Isolated nucleic acid molecules encoding human carbonate transporter proteins, and uses thereof

The present invention is in the field of transporter proteins that are related to the sodium bicarbonate cotransporter subfamily, recombinant DNA molecules, and protein production. The present invention specifically provides novel peptides and proteins that effect ligand transport and nucleic acid molecules encoding such peptide and protein molecules, all of which are useful in the development of human therapeutics and diagnostic compositions and methods.

Transporters

Transporter proteins regulate many different functions of a cell, including cell proliferation, differentiation, and signaling processes, by regulating the flow of molecules such as ions and macromolecules, into and out of cells. Transporters are found in the plasma membranes of virtually every cell in eukaryotic organisms. Transporters mediate a variety of cellular functions including regulation of membrane potentials and absorption and secretion of molecules and ion across cell membranes. When present in intracellular membranes of the Golgi apparatus and endocytic vesicles, transporters, such as chloride channels, also regulate organelle pH. For a review, see Greger, R. (1988) Annu. Rev. Physiol. 50: 111-122.

Transporters are generally classified by structure and the type of mode of action. In addition, transporters are sometimes classified by the molecule type that is transported, for example, sugar transporters, chlorine channels, potassium channels, etc. There may be many classes of channels for transporting a single type of molecule (a detailed review of channel types can be found at Alexander, S. P. H. and J. A. Peters: Receptor and transporter nomenclature supplement. Trends Pharmacol. Sci., Elsevier, pp. 65-68 (1997).

The following general classification scheme is known in the art and is followed in the present discoveries.

Channel-type transporters. Transmembrane channel proteins of this class are ubiquitously found in the membranes of all types of organisms from bacteria to higher eukaryotes. Transport systems of this type catalyze facilitated diffusion (by an energy-independent process) by passage through a transmembrane aqueous pore or channel without evidence for a carrier-mediated mechanism. These channel proteins usually consist largely of a-helical spanners, although b-strands may also be present and may even comprise the channel. However, outer membrane porin-type channel proteins are excluded from this class and are instead included in class 9.

Carrier-type transporters. Transport systems are included in this class if they utilize a carrier-mediated process to catalyze uniport (a single species is transported by facilitated diffusion), antiport (two or more species are transported in opposite directions in a tightly coupled process, not coupled to a direct form of energy other than chemiosmotic energy) and/or symport (two or more species are transported together in the same direction in a tightly coupled process, not coupled to a direct form of energy other than chemiosmotic energy).

Pyrophosphate bond hydrolysis-driven active transporters. Transport systems are included in this class if they hydrolyze pyrophosphate or the terminal pyrophosphate bond in ATP or another nucleoside triphosphate to drive the active uptake and/or extrusion of a solute or solutes. The transport protein may or may not be transiently phosphorylated, but the substrate is not phosphorylated.

PEP-dependent, phosphoryl transfer-driven group translocators. Transport systems of the bacterial phosphoenolpyruvate:sugar phosphotransferase system are included in this class. The product of the reaction, derived from extracellular sugar, is a cytoplasmic sugar-phosphate.

Decarboxylation-driven active transporters. Transport systems that drive solute (e.g., ion) uptake or extrusion by decarboxylation of a cytoplasmic substrate are included in this class.

Oxidoreduction-driven active transporters. Transport systems that drive transport of a solute (e.g., an ion) energized by the flow of electrons from a reduced substrate to an oxidized substrate are included in this class.

Light-driven active transporters. Transport systems that utilize light energy to drive transport of a solute (e.g., an ion) are included in this class.

Mechanically-driven active transporters. Transport systems are included in this class if they drive movement of a cell or organelle by allowing the flow of ions (or other solutes) through the membrane down their electrochemical gradients.

Outer-membrane porins (of b-structure). These proteins form transmembrane pores or channels that usually allow the energy independent passage of solutes across a membrane. The transmembrane portions of these proteins consist exclusively of b-strands that form a b-barrel. These porin-type proteins are found in the outer membranes of Gram-negative bacteria, mitochondria and eukaryotic plastids.

Methyltransferase-driven active transporters. A single characterized protein currently falls into this category, the Na+-transporting methyltetrahydromethanopterin:coenzyme M methyltransferase.

Non-ribosome-synthesized channel-forming peptides or peptide-like molecules. These molecules, usually chains of L- and D-amino acids as well as other small molecular building blocks such as lactate, form oligomeric transmembrane ion channels. Voltage may induce channel formation by promoting assembly of the transmembrane channel. These peptides are often made by bacteria and fungi as agents of biological warfare.

Non-Proteinaceous Transport Complexes. Ion conducting substances in biological membranes that do not consist of or are not derived from proteins or peptides fall into this category.

Functionally characterized transporters for which sequence data are lacking. Transporters of particular physiological significance will be included in this category even though a family assignment cannot be made.

Putative transporters in which no family member is an established transporter. Putative transport protein families are grouped under this number and will either be classified elsewhere when the transport function of a member becomes established, or will be eliminated from the TC classification system if the proposed transport function is disproven. These families include a member or members for which a transport function has been suggested, but evidence for such a function is not yet compelling.

Auxiliary transport proteins. Proteins that in some way facilitate transport across one or more biological membranes but do not themselves participate directly in transport are included in this class. These proteins always function in conjunction with one or more transport proteins. They may provide a function connected with energy coupling to transport, play a structural role in complex formation or serve a regulatory function.

Transporters of unknown classification. Transport protein families of unknown classification are grouped under this number and will be classified elsewhere when the transport process and energy coupling mechanism are characterized. These families include at least one member for which a transport function has been established, but either the mode of transport or the energy coupling mechanism is not known.

Ion Channels

An important type of transporter is the ion channel. Ion channels regulate many different cell proliferation, differentiation, and signaling processes by regulating the flow of ions into and out of cells. Ion channels are found in the plasma membranes of virtually every cell in eukaryotic organisms. Ion channels mediate a variety of cellular functions including regulation of membrane potentials and absorption and secretion of ion across epithelial membranes. When present in intracellular membranes of the Golgi apparatus and endocytic vesicles, ion channels, such as chloride channels, also regulate organelle pH. For a review, see Greger, R. (1988) Annu. Rev. Physiol. 50: 111-122.

Ion channels are generally classified by structure and the type of mode of action. For example, extracellular ligand gated channels (ELGs) are comprised of five polypeptide subunits, with each subunit having 4 membrane spanning domains, and are activated by the binding of an extracellular ligand to the channel. In addition, channels are sometimes classified by the ion type that is transported, for example, chlorine channels, potassium channels, etc. There may be many classes of channels for transporting a single type of ion (a detailed review of channel types can be found at Alexander, S. P. H. and J. A. Peters (1997). Receptor and ion channel nomenclature supplement. Trends Pharmacol. Sci., Elsevier, pp. 65-68.

There are many types of ion channels based on structure. For example, many ion channels fall within one of the following groups: extracellular ligand-gated channels (ELG), intracellular ligand-gated channels (ILG), inward rectifying channels (INR), intercellular (gap junction) channels, and voltage gated channels (VIC). There are additionally recognized other channel families based on ion-type transported, cellular location and drug sensitivity. Detailed information on each of these, their activity, ligand type, ion type, disease association, drugability, and other information pertinent to the present invention, is well known in the art.

Extracellular ligand-gated channels, ELGs, are generally comprised of five polypeptide subunits, Unwin, N. (1993), Cell 72: 31-41; Unwin, N. (1995), Nature 373: 37-43; Hucho, F., et al., (1996) J. Neurochem. 66: 1781-1792; Hucho, F., et al., (1996) Eur. J. Biochem. 239: 539-557; Alexander, S. P. H. and J. A. Peters (1997), Trends Pharmacol. Sci., Elsevier, pp. 4-6; 36-40; 42-44; and Xue, H. (1998) J. Mol. Evol. 47: 323-333. Each subunit has 4 membrane spanning regions: this serves as a means of identifying other members of the ELG family of proteins. ELG bind a ligand and in response modulate the flow of ions. Examples of ELG include most members of the neurotransmitter-receptor family of proteins, e.g., GABAI receptors. Other members of this family of ion channels include glycine receptors, ryandyne receptors, and ligand gated calcium channels.

The Voltage-gated Ion Channel (VIC) Superfamily

Proteins of the VIC family are ion-selective channel proteins found in a wide range of bacteria, archaea and eukaryotes Hille, B. (1992), Chapter 9: Structure of channel proteins; Chapter 20: Evolution and diversity. In: Ionic Channels of Excitable Membranes, 2nd Ed., Sinaur Assoc. Inc., Pubs., Sunderland, Mass.; Sigworth, F. J. (1993), Quart. Rev. Biophys. 27: 1-40; Salkoff, L. and T. Jegla (1995), Neuron 15: 489-492; Alexander, S. P. H. et al., (1997), Trends Pharmacol. Sci., Elsevier, pp. 76-84; Jan, L. Y. et al., (1997), Annu. Rev. Neurosci. 20: 91-123; Doyle, D. A, et al., (1998) Science 280: 69-77; Terlau, H. and W. Stühmer (1998), Naturwissenschaften 85: 437-444. They are often homo- or heterooligomeric structures with several dissimilar subunits (e.g., a1-a2-d-b Ca 2+ channels, ab 1 b 2 Na + channels or (a) 4 -b K + channels), but the channel and the primary receptor is usually associated with the a (or al) subunit. Functionally characterized members are specific for K + , Na + or Ca 2+ . The K + channels usually consist of homotetrameric structures with each a-subunit possessing six transmembrane spanners (TMSs). The al and a subunits of the Ca 2+ and Na + channels, respectively, are about four times as large and possess 4 units, each with 6 TMSs separated by a hydrophilic loop, for a total of 24 TMSs. These large channel proteins form heterotetra-unit structures equivalent to the homotetrameric structures of most K + channels. All four units of the Ca 2+ and Na + channels are homologous to the single unit in the homotetrameric K + channels. Ion flux via the eukaryotic channels is generally controlled by the transmembrane electrical potential (hence the designation, voltage-sensitive) although some are controlled by ligand or receptor binding.

Several putative K + -selective channel proteins of the VIC family have been identified in prokaryotes. The structure of one of them, the KcsA K + channel of Streptomyces lividans, has been solved to 3.2 Å resolution. The protein possesses four identical subunits, each with two transmembrane helices, arranged in the shape of an inverted teepee or cone. The cone cradles the “selectivity filter” P domain in its outer end. The narrow selectivity filter is only 12 Å long, whereas the remainder of the channel is wider and lined with hydrophobic residues. A large water-filled cavity and helix dipoles stabilize K + in the pore. The selectivity filter has two bound K + ions about 7.5 Å apart from each other. Ion conduction is proposed to result from a balance of electrostatic attractive and repulsive forces.

In eukaryotes, each VIC family channel type has several subtypes based on pharmacological and electrophysiological data. Thus, there are five types of Ca 2+ channels (L, N, P, Q and T). There are at least ten types of K + channels, each responding in different ways to different stimuli: voltage-sensitive [Ka, Kv, Kvr, Kvs and Ksr], Ca 2+ -sensitive [BK Ca , IK Ca and SK Ca ] and receptor-coupled [K M and K ACh ]. There are at least six types of Na + channels (I, II, III, μ1, H1 and PN3). Tetrameric channels from both prokaryotic and eukaryotic organisms are known in which each a-subunit possesses 2 TMSs rather than 6, and these two TMSs are homologous to TMSs 5 and 6 of the six TMS unit found in the voltage-sensitive channel proteins. KcsA of S. lividans is an example of such a 2 TMS channel protein. These channels may include the K Na (Na + -activated) and K Vol (cell volume-sensitive) K + channels, as well as distantly related channels such as the Tok1 K + channel of yeast, the TWIK-1 inward rectifier K + channel of the mouse and the TREK-1 K + channel of the mouse. Because of insufficient sequence similarity with proteins of the VIC family, inward rectifier K + IRK channels (ATP-regulated; G-protein-activated) which possess a P domain and two flanking TMSs are placed in a distinct family. However, substantial sequence similarity in the P region suggests that they are homologous. The b, g and d subunits of VIC family members, when present, frequently play regulatory roles in channel activation/deactivation.

The Epithelial Na + Channel (ENaC) Family

The ENaC family consists of over twenty-four sequenced proteins (Canessa, C. M., et al., (1994), Nature 367: 463-467, Le, T. and M. H. Saier, Jr. (1996), Mol. Membr. Biol. 13: 149-157; Garty, H. and L. G. Palmer (1997), Physiol. Rev. 77: 359-396; Waldmann, R., et al., (1997), Nature 386: 173-177; Darboux, I., et al., (1998), J. Biol. Chem. 273: 9424-9429; Firsov, D., et al., (1998), EMBO J. 17: 344-352; Horisberger, J. D. (1998). Curr. Opin. Struc. Biol. 10: 443-449). All are from animals with no recognizable homologues in other eukaryotes or bacteria. The vertebrate ENaC proteins from epithelial cells cluster tightly together on the phylogenetic tree: voltage-insensitive ENaC homologues are also found in the brain. Eleven sequenced C. elegans proteins, including the degenerins, are distantly related to the vertebrate proteins as well as to each other. At least some of these proteins form part of a mechano-transducing complex for touch sensitivity. The homologous Helix aspersa (FMRF-amide)-activated Na + channel is the first peptide neurotransmitter-gated ionotropic receptor to be sequenced.

Protein members of this family all exhibit the same apparent topology, each with N- and C-termini on the inside of the cell, two amphipathic transmembrane spanning segments, and a large extracellular loop. The extracellular domains contain numerous highly conserved cysteine residues. They are proposed to serve a receptor function.

Mammalian ENaC is important for the maintenance of Na + balance and the regulation of blood pressure. Three homologous ENaC subunits, alpha, beta, and gamma, have been shown to assemble to form the highly Na + -selective channel. The stoichiometry of the three subunits is alpha 2 beta1, gamma1 in a heterotetrameric architecture.

The Glutamate-gated Ion Channel (GIC) Family of Neurotransmitter Receptors

Members of the GIC family are heteropentameric complexes in which each of the 5 subunits is of 800-1000 amino acyl residues in length (Nakanishi, N., et al, (1990), Neuron 5: 569-581; Unwin, N. (1993), Cell 72: 31-41; Alexander, S. P. H. and J. A. Peters (1997) Trends Pharmacol. Sci., Elsevier, pp. 36-40). These subunits may span the membrane three or five times as putative a-helices with the N-termini (the glutamate-binding domains) localized extracellularly and the C-termini localized cytoplasmically. They may be distantly related to the ligand-gated ion channels, and if so, they may possess substantial b-structure in their transmembrane regions. However, homology between these two families cannot be established on the basis of sequence comparisons alone. The subunits fall into six subfamilies: a, b, g, d, e and z.

The GIC channels are divided into three types: (1) a-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA)-, (2) kainate- and (3) N-methyl-D-aspartate (NMDA)-selective glutamate receptors. Subunits of the AMPA and kainate classes exhibit 35-40% identity with each other while subunits of the NMDA receptors exhibit 22-24% identity with the former subunits. They possess large N-terminal, extracellular glutamate-binding domains that are homologous to the periplasmic glutamine and glutamate receptors of ABC-type uptake permeases of Gram-negative bacteria. All known members of the GIC family are from animals. The different channel (receptor) types exhibit distinct ion selectivities and conductance properties. The NMDA-selective large conductance channels are highly permeable to monovalent cations and Ca 2+ . The AMPA- and kainate-selective ion channels are permeable primarily to monovalent cations with only low permeability to Ca 2+ .

The Chloride Channel (ClC) Family

The ClC family is a large family consisting of dozens of sequenced proteins derived from Gram-negative and Gram-positive bacteria, cyanobacteria, archaea, yeast, plants and animals (Steinmeyer, K., et al., (1991), Nature 354: 301-304; Uchida, S., et al., (1993), J. Biol. Chem. 268: 3821-3824; Huang, M.-E., et al., (1994), J. Mol. Biol. 242: 595-598; Kawasaki, M., et al, (1994), Neuron 12: 597-604; Fisher, W. E., et al., (1995), Genomics. 29:598-606; and Foskett, J. K. (1998), Annu. Rev. Physiol. 60: 689-717). These proteins are essentially ubiquitous, although they are not encoded within genomes of Haemophilus influenzae, Mycoplasma genitalium, and Mycoplasma pneumoniae. Sequenced proteins vary in size from 395 amino acyl residues ( M. jannaschii ) to 988 residues (man). Several organisms contain multiple ClC family paralogues. For example, Synechocystis has two paralogues, one of 451 residues in length and the other of 899 residues. Arabidopsis thaliana has at least four sequenced paralogues, (775-792 residues), humans also have at least five paralogues (820-988 residues), and C. elegans also has at least five (810-950 residues). There are nine known members in mammals, and mutations in three of the corresponding genes cause human diseases. E. coli, Methanococcus jannaschii and Saccharomyces cerevisiae only have one ClC family member each. With the exception of the larger Synechocystis paralogue, all bacterial proteins are small (395-492 residues) while all eukaryotic proteins are larger (687-988 residues). These proteins exhibit 10-12 putative transmembrane a-helical spanners (TMSs) and appear to be present in the membrane as homodimers. While one member of the family, Torpedo ClC-O, has been reported to have two channels, one per subunit, others are believed to have just one.

All functionally characterized members of the ClC family transport chloride, some in a voltage-regulated process. These channels serve a variety of physiological functions (cell volume regulation; membrane potential stabilization; signal transduction; transepithelial transport, etc.). Different homologues in humans exhibit differing anion selectivities, i.e., ClC4 and ClC5 share a NO 3 − >Cl − >Br 31 >I − conductance sequence, while ClC3 has an I − >Cl − selectivity. The ClC4 and ClC5 channels and others exhibit outward rectifying currents with currents only at voltages more positive than +20 mV.

Animal Inward Rectifier K + Channel (IRK-C) Family

IRK channels possess the “minimal channel-forming structure” with only a P domain, characteristic of the channel proteins of the VIC family, and two flanking transmembrane spanners (Shuck, M. E., et al., (1994), J. Biol. Chem. 269: 24261-24270; Ashen, M. D., et al., (1995), Am. J. Physiol. 268: H506-H511; Salkoff, L. and T. Jegla (1995), Neuron 15: 489-492; Aguilar-Bryan, L., et al., (1998), Physiol. Rev. 78: 227-245; Ruknudin, A., et al., (1998), J. Biol. Chem. 273: 14165-14171). They may exist in the membrane as homo- or heterooligomers. They have a greater tendency to let K + flow into the cell than out. Voltage-dependence may be regulated by external K + , by internal Mg 2+ , by internal ATP and/or by G-proteins. The P domains of IRK channels exhibit limited sequence similarity to those of the VIC family, but this sequence similarity is insufficient to establish homology. Inward rectifiers play a role in setting cellular membrane potentials, and the closing of these channels upon depolarization permits the occurrence of long duration action potentials with a plateau phase. Inward rectifiers lack the intrinsic voltage sensing helices found in VIC family channels. In a few cases, those of Kir.1.1a and Kir6.2, for example, direct interaction with a member of the ABC superfamily has been proposed to confer unique functional and regulatory properties to the heteromeric complex, including sensitivity to ATP. The SUR1 sulfonylurea receptor (spQ09428) is the ABC protein that regulates the Kir6.2 channel in response to ATP, and CFTR may regulate Kir1.1a. Mutations in SUR1 are the cause of familial persistent hyperinsulinemic hypoglycemia in infancy (PHHI), an autosomal recessive disorder characterized by unregulated insulin secretion in the pancreas.

ATP-gated Cation Channel (ACC) Family

Members of the ACC family (also called P2X receptors) respond to ATP, a functional neurotransmitter released by exocytosis from many types of neurons (North, R. A. (1996), Curr. Opin. Cell Biol. 8: 474-483; Soto, F., M. Garcia-Guzman and W. Stühmer (1997), J. Membr. Biol. 160: 91-100). They have been placed into seven groups (P2X 1 -P2X 7 ) based on their pharmacological properties. These channels, which function at neuron-neuron and neuron-smooth muscle junctions, may play roles in the control of blood pressure and pain sensation. They may also function in lymphocyte and platelet physiology. They are found only in animals.

The proteins of the ACC family are quite similar in sequence (>35% identity), but they possess 380-1000 amino acyl residues per subunit with variability in length localized primarily to the C-terminal domains. They possess two transmembrane spanners, one about 30-50 residues from their N-termini, the other near residues 320-340. The extracellular receptor domains between these two spanners (of about 270 residues) are well conserved with numerous conserved glycyl and cysteyl residues. The hydrophilic C-termini vary in length from 25 to 240 residues. They resemble the topologically similar epithelial Na + channel (ENaC) proteins in possessing (a) N- and C-termini localized intracellularly, (b) two putative transmembrane spanners, (c) a large extracellular loop domain, and (d) many conserved extracellular cysteyl residues. ACC family members are, however, not demonstrably homologous with them. ACC channels are probably hetero- or homomultimers and transport small monovalent cations (Me + ). Some also transport Ca 2+ ; a few also transport small metabolites.

The Ryanodine-Inositol 1,4,5-triphosphate Receptor Ca 2+ Channel (RIR-CaC) Family

Ryanodine (Ry)-sensitive and inositol 1,4,5-triphosphate (IP3)-sensitive Ca 2+ -release channels function in the release of Ca 2+ from intracellular storage sites in animal cells and thereby regulate various Ca 2+ -dependent physiological processes (Hasan, G. et al., (1992) Development 116: 967-975; Michikawa, T., et al., (1994), J. Biol. Chem. 269: 9184-9189; Tunwell, R. E. A., (1996), Biochem. J. 318: 477-487; Lee, A. G. (1996) Biomembranes, Vol. 6, Transmembrane Receptors and Channels (A. G. Lee, ed.), JAI Press, Denver, Colo., pp 291-326; Mikoshiba, K., et al., (1996) J. Biochem. Biomem. 6: 273-289). Ry receptors occur primarily in muscle cell sarcoplasmic reticular (SR) membranes, and IP3 receptors occur primarily in brain cell endoplasmic reticular (ER) membranes where they effect release of Ca 2+ into the cytoplasm upon activation (opening) of the channel.

The Ry receptors are activated as a result of the activity of dihydropyridine-sensitive Ca 2+ channels. The latter are members of the voltage-sensitive ion channel (VIC) family. Dihydropyridine-sensitive channels are present in the T-tubular systems of muscle tissues.

Ry receptors are homotetrameric complexes with each subunit exhibiting a molecular size of over 500,000 daltons (about 5,000 amino acyl residues). They possess C-terminal domains with six putative transmembrane a -helical spanners (TMSs). Pulative pore-forming sequences occur between the fifth and sixth TMSs as suggested for members of the VIC family. The large N-terminal hydrophilic domains and the small C-terminal hydrophilic domains are localized to the cytoplasm. Low resolution 3-dimensional structural data are available. Mammals possess at least three isoforms that probably arose by gene duplication and divergence before divergence of the mammalian species. Homologues are present in humans and Caenorabditis elegans.

IP 3 receptors resemble Ry receptors in many respects. (1) They are homotetrameric complexes with each subunit exhibiting a molecular size of over 300,000 daltons (about 2,700 amino acyl residues). (2) They possess C-terminal channel domains that are homologous to those of the Ry receptors. (3) The channel domains possess six putative TMSs and a putative channel lining region between TMSs 5 and 6. (4) Both the large N-terminal domains and the smaller C-terminal tails face the cytoplasm. (5) They possess covalently linked carbohydrate on extracytoplasmic loops of the channel domains. (6) They have three currently recognized isoforms (types 1, 2, and 3) in mammals which are subject to differential regulation and have different tissue distributions.

IP 3 receptors possess three domains: N-terminal IP 3 -binding domains, central coupling or regulatory domains and C-terminal channel domains. Channels are activated by IP 3 binding, and like the Ry receptors, the activities of the IP 3 receptor channels are regulated by phosphorylation of the regulatory domains, catalyzed by various protein kinases. They predominate in the endoplasmic reticular membranes of various cell types in the brain but have also been found in the plasma membranes of some nerve cells derived from a variety of tissues.

The channel domains of the Ry and IP 3 receptors comprise a coherent family that in spite of apparent structural similarities, do not show appreciable sequence similarity of the proteins of the VIC family. The Ry receptors and the IP 3 receptors cluster separately on the RIR-CaC family tree. They both have homologues in Drosophila. Based on the phylogenetic tree for the family, the family probably evolved in the following sequence: (1) A gene duplication event occurred that gave rise to Ry and IP 3 receptors in invertebrates. (2) Vertebrates evolved from invertebrates. (3) The three isoforms of each receptor arose as a result of two distinct gene duplication events. (4) These isoforms were transmitted to mammals before divergence of the mammalian species.

The Organellar Chloride Channel (O-ClC) Family

Proteins of the O-ClC family are voltage-sensitive chloride channels found in intracellular membranes but not the plasma membranes of animal cells (Landry, D, et al., (1993), J. Biol. Chem. 268: 14948-14955; Valenzuela, Set al., (1997), J. Biol. Chem. 272: 12575-12582; and Duncan, R. R., et al., (1997), J. Biol. Chem. 272: 23880-23886).

They are found in human nuclear membranes, and the bovine protein targets to the microsomes, but not the plasma membrane, when expressed in Xenopus laevis oocytes. These proteins are thought to function in the regulation of the membrane potential and in transepithelial ion absorption and secretion in the kidney. They possess two putative transmembrane a-helical spanners (TMSs) with cytoplasmic N- and C-termini and a large luminal loop that may be glycosylated. The bovine protein is 437 amino acyl residues in length and has the two putative TMSs at positions 223-239 and 367-385. The human nuclear protein is much smaller (241 residues). A C. elegans homologue is 260 residues long.

Sodium Bicarbonate Cotransporters

The novel human protein provided by the present invention is related to the family of sodium bicarbonate cotransporters, and shows a particularly high degree of similarity to the mouse sodium bicarbonate cotransporter isoform kNBC-3.

The sodium bicarbonate cotransporter provides the primary mechanism for transporting bicarbonate across the basolateral membrane in the kidney. At least three sodium bicarbonate cotransporter isoforms are located in the kidney and these may be functionally altered in various pathophysiologic states. For example, sodium bicarbonate cotransporter isoform 1 may be stimulated by metabolic acidosis, potassium depletion, and glucocorticoid excess and may be inhibited by bicarbonate loading or alkalosis. Sodium bicarbonate cotransporters are activated by cystic fibrosis transmembrane conductance regulator (CFTR) and play an important role in bicarbonate secretion in pancreatic duct cells. Furthermore, sodium bicarbonate cotransporters may play an important role in acid-base disorders such as proximal renal tubular acidosis (Soleimani et al., Kidney Int 2000 February;57(2):371-84).

The sodium-driven chloride/bicarbonate exchanger plays an important role in regulating intracellular pH in a wide variety cells by transporting extracellular sodium and bicarbonate into cells in exchange for intracellular chloride and H(+), thereby raising intracellular pH (Wang et al, J Biol Chem Nov. 10, 2000;275(45):35486-90).

Transporter proteins, particularly members of the sodium bicarbonate cotransporter subfamily, are a major target for drug action and development. Accordingly, it is valuable to the field of pharmaceutical development to identify and characterize previously unknown transport proteins. The present invention advances the state of the art by providing previously unidentified human transport proteins.

The present invention is based in part on the identification of amino acid sequences of human transporter peptides and proteins that are related to the sodium bicarbonate cotransporter subfamily, as well as allelic variants and other mammalian orthologs thereof. These unique peptide sequences, and nucleic acid sequences that encode these peptides, can be used as models for the development of human therapeutic targets, aid in the identification of therapeutic proteins, and serve as targets for the development of human therapeutic agents that modulate transporter activity in cells and tissues that express the transporter. Experimental data as provided in FIG. 1 indicates expression in humans in the testis, brain (adult and fetal), placenta, and bone marrow.

FIGS. 1A-1D provide the nucleotide sequence of a cDNA molecule that encodes the transporter protein of the present invention. In addition structure and functional information is provided, such as ATG start, stop and tissue distribution, where available, that allows one to readily determine specific uses of inventions based on this molecular sequence. Experimental data as provided in FIG. 1 indicates expression in humans in the testis, brain (adult and fetal), placenta, and bone marrow.

FIGS. 2A-2G provide the predicted amino acid sequence of the transporter of the present invention. In addition structure and functional information such as protein family, function, and modification sites is provided where available, allowing one to readily determine specific uses of inventions based on this molecular sequence.

FIGS. 3 A- 3 GGGGG provide genomic sequences that span the gene encoding the transporter protein of the present invention. In addition structure and functional information, such as intron/exon structure, promoter location, etc., is provided where available, allowing one to readily determine specific uses of inventions based on this molecular sequence. As illustrated in FIG. 3, SNPs, including insertion/deletion polymorphisms (“indels”), were identifed at 87 different nucleotide positions.

General Description

The present invention is based on the sequencing of the human genome. During the sequencing and assembly of the human genome, analysis of the sequence information revealed previously unidentified fragments of the human genome that encode peptides that share structural and/or sequence homology to protein/peptide/domains identified and characterized within the art as being a transporter protein or part of a transporter protein and are related to the sodium bicarbonate cotransporter subfamily. Utilizing these sequences, additional genomic sequences were assembled and transcript and/or cDNA sequences were isolated and characterized. Based on this analysis, the present invention provides amino acid sequences of human transporter peptides and proteins that are related to the sodium bicarbonate cotransporter subfamily, nucleic acid sequences in the form of transcript sequences, cDNA sequences and/or genomic sequences that encode these transporter peptides and proteins, nucleic acid variation (allelic information), tissue distribution of expression, and information about the closest art known protein/peptide/domain that has structural or sequence homology to the transporter of the present invention.

In addition to being previously unknown, the peptides that are provided in the present invention are selected based on their ability to be used for the development of commercially important products and services. Specifically, the present peptides are selected based on homology and/or structural relatedness to known transporter proteins of the sodium bicarbonate cotransporter subfamily and the expression pattern observed. Experimental data as provided in FIG. 1 indicates expression in humans in the testis, brain (adult and fetal), placenta, and bone marrow. The art has clearly established the commercial importance of members of this family of proteins and proteins that have expression patterns similar to that of the present gene. Some of the more specific features of the peptides of the present invention, and the uses thereof, are described herein, particularly in the Background of the Invention and in the annotation provided in the Figures, and/or are known within the art for each of the known sodium bicarbonate cotransporter family or subfamily of transporter proteins.

Specific Embodiments

Peptide Molecules

The present invention provides nucleic acid sequences that encode protein molecules that have been identified as being members of the transporter family of proteins and are related to the sodium bicarbonate cotransporter subfamily (protein sequences are provided in FIG. 2, transcript/cDNA sequences are provided in FIGS. 1 and genomic sequences are provided in FIG. 3 ). The peptide sequences provided in FIG. 2, as well as the obvious variants described herein, particularly allelic variants as identified herein and using the information in FIG. 3, will be referred herein as the transporter peptides of the present invention, transporter peptides, or peptides/proteins of the present invention.

The present invention provides isolated peptide and protein molecules that consist of, consist essentially of, or comprising the amino acid sequences of the transporter peptides disclosed in the FIG. 2, (encoded by the nucleic acid molecule shown in FIG. 1, transcript/cDNA or FIG. 3, genomic sequence), as well as all obvious variants of these peptides that are within the art to make and use. Some of these variants are described in detail below.

As used herein, a peptide is said to be “isolated” or “purified” when it is substantially free of cellular material or free of chemical precursors or other chemicals. The peptides of the present invention can be purified to homogeneity or other degrees of purity. The level of purification will be based on the intended use. The critical feature is that the preparation allows for the desired function of the peptide, even if in the presence of considerable amounts of other components (the features of an isolated nucleic acid molecule is discussed below).

In some uses, “substantially free of cellular material” includes preparations of the peptide having less than about 30% (by dry weight) other proteins (i.e., contaminating protein), less than about 20% other proteins, less than about 10% other proteins, or less than about 5% other proteins. When the peptide is recombinantly produced, it can also be substantially free of culture medium, i.e., culture medium represents less than about 20% of the volume of the protein preparation.

The language “substantially free of chemical precursors or other chemicals” includes preparations of the peptide in which it is separated from chemical precursors or other chemicals that are involved in its synthesis. In one embodiment, the language “substantially free of chemical precursors or other chemicals” includes preparations of the transporter peptide having less than about 30% (by dry weight) chemical precursors or other chemicals, less than about 20% chemical precursors or other chemicals, less than about 10% chemical precursors or other chemicals, or less than about 5% chemical precursors or other chemicals.

The isolated transporter peptide can be purified from cells that naturally express it, purified from cells that have been altered to express it (recombinant), or synthesized using known protein synthesis methods. Experimental data as provided in FIG. 1 indicates expression in humans in the testis, brain (adult and fetal), placenta, and bone marrow. For example, a nucleic acid molecule encoding the transporter peptide is cloned into an expression vector, the expression vector introduced into a host cell and the protein expressed in the host cell. The protein can then be isolated from the cells by an appropriate purification scheme using standard protein purification techniques. Many of these techniques are described in detail below.

Accordingly, the present invention provides proteins that consist of the amino acid sequences provided in FIG. 2 (SEQ ID NO:2), for example, proteins encoded by the transcript/cDNA nucleic acid sequences shown in FIG. 1 (SEQ ID NO:1) and the genomic sequences provided in FIG. 3 (SEQ ID NO:3). The amino acid sequence of such a protein is provided in FIG. 2. A protein consists of an amino acid sequence when the amino acid sequence is the final amino acid sequence of the protein.

The present invention further provides proteins that consist essentially of the amino acid sequences provided in FIG. 2 (SEQ ID NO:2), for example, proteins encoded by the transcript/cDNA nucleic acid sequences shown in FIG. 1 (SEQ ID NO:1) and the genomic sequences provided in FIG. 3 (SEQ ID NO:3). A protein consists essentially of an amino acid sequence when such an amino acid sequence is present with only a few additional amino acid residues, for example from about 1 to about 100 or so additional residues, typically from 1 to about 20 additional residues in the final protein.

The present invention further provides proteins that comprise the amino acid sequences provided in FIG. 2 (SEQ ID NO:2), for example, proteins encoded by the transcript/cDNA nucleic acid sequences shown in FIG. 1 (SEQ ID NO:1) and the genomic sequences provided in FIG. 3 (SEQ ID NO:3). A protein comprises an amino acid sequence when the amino acid sequence is at least part of the final amino acid sequence of the protein. In such a fashion, the protein can be only the peptide or have additional amino acid molecules, such as amino acid residues (contiguous encoded sequence) that are naturally associated with it or heterologous amino acid residues/peptide sequences. Such a protein can have a few additional amino acid residues or can comprise several hundred or more additional amino acids. The preferred classes of proteins that are comprised of the transporter peptides of the present invention are the naturally occurring mature proteins. A brief description of how various types of these proteins can be made/isolated is provided below.

The transporter peptides of the present invention can be attached to heterologous sequences to form chimeric or fusion proteins. Such chimeric and fusion proteins comprise a transporter peptide operatively linked to a heterologous protein having an amino acid sequence not substantially homologous to the transporter peptide. “Operatively linked” indicates that the transporter peptide and the heterologous protein are fused in-frame. The heterologous protein can be fused to the N-terminus or C-terminus of the transporter peptide.

In some uses, the fusion protein does not affect the activity of the transporter peptide per se. For example, the fusion protein can include, but is not limited to, enzymatic fusion proteins, for example beta-galactosidase fusions, yeast two-hybrid GAL fusions, poly-His fusions, MYC-tagged, HI-tagged and Ig fusions. Such fusion proteins, particularly poly-His fusions, can facilitate the purification of recombinant transporter peptide. In certain host cells (e.g., mammalian host cells), expression and/or secretion of a protein can be increased by using a heterologous signal sequence.

A chimeric or fusion protein can be produced by standard recombinant DNA techniques. For example, DNA fragments coding for the different protein sequences are ligated together in-frame in accordance with conventional techniques. In another embodiment, the fusion gene can be synthesized by conventional techniques including automated DNA synthesizers. Alternatively, PCR amplification of gene fragments can be carried out using anchor primers which give rise to complementary overhangs between two consecutive gene fragments which can subsequently be annealed and re-amplified to generate a chimeric gene sequence (see Ausubel et al., Current Protocols in Molecular Biology, 1992). Moreover, many expression vectors are commercially available that already encode a fusion moiety (e.g., a GST protein). A transporter peptide-encoding nucleic acid can be cloned into such an expression vector such that the fusion moiety is linked in-frame to the transporter peptide.

As mentioned above, the present invention also provides and enables obvious variants of the amino acid sequence of the proteins of the present invention, such as naturally occurring mature forms of the peptide, allelic/sequence variants of the peptides, non-naturally occurring recombinantly derived variants of the peptides, and orthologs and paralogs of the peptides. Such variants can readily be generated using art-known techniques in the fields of recombinant nucleic acid technology and protein biochemistry. It is understood, however, that variants exclude any amino acid sequences disclosed prior to the invention.

Such variants can readily be identified/made using molecular techniques and the sequence information disclosed herein. Further, such variants can readily be distinguished from other peptides based on sequence and/or structural homology to the transporter peptides of the present invention. The degree of homology/identity present will be based primarily on whether the peptide is a functional variant or non-functional variant, the amount of divergence present in the paralog family and the evolutionary distance between the orthologs.

To determine the percent identity of two amino acid sequences or two nucleic acid sequences, the sequences are aligned for optimal comparison purposes (e.g., gaps can be introduced in one or both of a first and a second amino acid or nucleic acid sequence for optimal alignment and non-homologous sequences can be disregarded for comparison purposes). In a preferred embodiment, at least 30%, 40%, 50%, 60%, 70%, 80%, or 90% or more of a reference sequence is aligned for comparison purposes. The amino acid residues or nucleotides at corresponding amino acid positions or nucleotide positions are then compared. When a position in the first sequence is occupied by the same amino acid residue or nucleotide as the corresponding position in the second sequence, then the molecules are identical at that position (as used herein amino acid or nucleic acid “identity” is equivalent to amino acid or nucleic acid “homology”). The percent identity between the two sequences is a function of the number of identical positions shared by the sequences, taking into account the number of gaps, and the length of each gap, which need to be introduced for optimal alignment of the two sequences.

The comparison of sequences and determination of percent identity and similarity between two sequences can be accomplished using a mathematical algorithm. ( Computational Molecular Biology, Lesk, A. M., ed., Oxford University Press, N.Y., 1988; Biocomputing: Informatics and Genome Projects, Smith, D. W., ed., Academic Press, N.Y., 1993; Computer Analysis of Sequence Data, Part 1, Griffin, A. M., and Griffin, H. G., eds., Humana Press, N. J., 1994; Sequence Analysis in Molecular Biology, von Heinje, G., Academic Press, 1987; and Sequence Analysis Primer, Gribskov, M. and Devereux, J., eds., M Stockton Press, N. Y., 1991). In a preferred embodiment, the percent identity between two amino acid sequences is determined using the Needleman and Wunsch (J. Mol. Biol. (48):444-453 (1970)) algorithm which has been incorporated into the GAP program in the GCG software package, using either a Blossom 62 matrix or a PAM250 matrix, and a gap weight of 16, 14, 12, 10, 8, 6, or 4 and a length weight of 1, 2, 3, 4, 5, or 6. In yet another preferred embodiment, the percent identity between two nucleotide sequences is determined using the GAP program in the GCG software package (Devereux, J., et al., Nucleic Acids Res. 12(1):387 (1984)), using a NWSgapdna.CMP matrix and a gap weight of 40, 50, 60, 70, or 80 and a length weight of 1, 2, 3, 4, 5, or 6. In another embodiment, the percent identity between two amino acid or nucleotide sequences is determined using the algorithm of E. Myers and W. Miller (CABIOS, 4:11-17 (1989)) which has been incorporated into the ALIGN program (version 2.0), using a PAM120 weight residue table, a gap length penalty of 12 and a gap penalty of 4.

The nucleic acid and protein sequences of the present invention can further be used as a “query sequence” to perform a search against sequence databases to, for example, identify other family members or related sequences. Such searches can be performed using the NBLAST and XBLAST programs (version 2.0) of Altschul, et al. ( J. Mol. Biol. 215:403-10 (1990)). BLAST nucleotide searches can be performed with the NBLAST program, score=100, wordlength=12 to obtain nucleotide sequences homologous to the nucleic acid molecules of the invention. BLAST protein searches can be performed with the XBLAST program, score=50, wordlength=3 to obtain amino acid sequences homologous to the proteins of the invention. To obtain gapped alignments for comparison purposes, Gapped BLAST can be utilized as described in Altschul et al. ( Nucleic Acids Res. 25(17):3389-3402 (1997)). When utilizing BLAST and gapped BLAST programs, the default parameters of the respective programs (e.g., XBLAST and NBLAST) can be used.

Full-length pre-processed forms, as well as mature processed forms, of proteins that comprise one of the peptides of the present invention can readily be identified as having complete sequence identity to one of the transporter peptides of the present invention as well as being encoded by the same genetic locus as the transporter peptide provided herein. As indicated by the data presented in FIG. 3, the gene provided by the present invention is located on public BAC AC008063.2, which is known to be mapped to chromosome 2.

Allelic variants of a transporter peptide can readily be identified as being a human protein having a high degree (significant) of sequence homology/identity to at least a portion of the transporter peptide as well as being encoded by the same genetic locus as the transporter peptide provided herein. Genetic locus can readily be determined based on the genomic information provided in FIG. 3, such as the genomic sequence mapped to the reference human. As indicated by the data presented in FIG. 3, the gene provided by the present invention is located on public BAC AC008063.2, which is known to be mapped to chromosome 2. As used herein, two proteins (or a region of the proteins) have significant homology when the amino acid sequences are typically at least about 70-80%, 80-90%, and more typically at least about 90-95% or more homologous. A significantly homologous amino acid sequence, according to the present invention, will be encoded by a nucleic acid sequence that will hybridize to a transporter peptide encoding nucleic acid molecule under stringent conditions as more fully described below.

FIG. 3 provides information on SNPs that have been found in the gene encoding the transporter protein of the present invention. SNPs, including insertion/deletion polymorphisms (“indels”), were identifed at 87 different nucleotide positions. Changes in the amino acid sequence caused by these SNPs can readily be determined using the universal genetic code and the protein sequence provided in FIG. 2 as a reference. SNPs outside the ORF and in introns may affect control/regulatory elements. SNP positioning in exons, introns, or outside the ORF can readily be determined based on the genomic features given in FIG. 3 .

Paralogs of a transporter peptide can readily be identified as having some degree of significant sequence homology/identity to at least a portion of the transporter peptide, as being encoded by a gene from humans, and as having similar activity or function. Two proteins will typically be considered paralogs when the amino acid sequences are typically at least about 60% or greater, and more typically at least about 70% or greater homology through a given region or domain. Such paralogs will be encoded by a nucleic acid sequence that will hybridize to a transporter peptide encoding nucleic acid molecule under moderate to stringent conditions as more fully described below.

Orthologs of a transporter peptide can readily be identified as having some degree of significant sequence homology/identity to at least a portion of the transporter peptide as well as being encoded by a gene from another organism. Preferred orthologs will be isolated from mammals, preferably primates, for the development of human therapeutic targets and agents. Such orthologs will be encoded by a nucleic acid sequence that will hybridize to a transporter peptide encoding nucleic acid molecule under moderate to stringent conditions, as more fully described below, depending on the degree of relatedness of the two organisms yielding the proteins.

Non-naturally occurring variants of the transporter peptides of the present invention can readily be generated using recombinant techniques. Such variants include, but are not limited to deletions, additions and substitutions in the amino acid sequence of the transporter peptide. For example, one class of substitutions are conserved amino acid substitution. Such substitutions are those that substitute a given amino acid in a transporter peptide by another amino acid of like characteristics. Typically seen as conservative substitutions are the replacements, one for another, among the aliphatic amino acids Ala, Val, Leu, and Ile; interchange of the hydroxyl residues Ser and Thr; exchange of the acidic residues Asp and Glu; substitution between the amide residues Asn and Gln; exchange of the basic residues Lys and Arg; and replacements among the aromatic residues Phe and Tyr. Guidance concerning which amino acid changes are likely to be phenotypically silent are found in Bowie et al., Science 247:1306-1310 (1990).

Variant transporter peptides can be fully functional or can lack function in one or more activities, e.g. ability to bind ligand, ability to transport ligand, ability to mediate signaling, etc. Fully functional variants typically contain only conservative variation or variation in non-critical residues or in non-critical regions. FIG. 2 provides the result of protein analysis and can be used to identify critical domains/regions. Functional variants can also contain substitution of similar amino acids that result in no change or an insignificant change in function. Alternatively, such substitutions may positively or negatively affect function to some degree.

Non-functional variants typically contain one or more non-conservative amino acid substitutions, deletions, insertions, inversions, or truncation or a substitution, insertion, inversion, or deletion in a critical residue or critical region.

Amino acids that are essential for function can be identified by methods known in the art, such as site-directed mutagenesis or alanine-scanning mutagenesis (Cunningham et al, Science 244:1081-1085 (1989)), particularly using the results provided in FIG. 2 . The latter procedure introduces single alanine mutations at every residue in the molecule. The resulting mutant molecules are then tested for biological activity such as transporter activity or in assays such as an in vitro proliferative activity. Sites that are critical for binding partner/substrate binding can also be determined by structural analysis such as crystallization, nuclear magnetic resonance or photoaffinity labeling (Smith et al., J. Mol. Biol. 224:899-904 (1992); de Vos et al. Science 255:306-312 (1992)).

The present invention further provides fragments of the transporter peptides, in addition to proteins and peptides that comprise and consist of such fragments, particularly those comprising the residues identified in FIG. 2 . The fragments to which the invention pertains, however, are not to be construed as encompassing fragments that may be disclosed publicly prior to the present invention.

As used herein, a fragment comprises at least 8, 10, 12, 14, 16, or more contiguous amino acid residues from a transporter peptide. Such fragments can be chosen based on the ability to retain one or more of the biological activities of the transporter peptide or could be chosen for the ability to perform a function, e.g. bind a substrate or act as an immunogen. Particularly important fragments are biologically active fragments, peptides that are, for example, about 8 or more amino acids in length. Such fragments will typically comprise a domain or motif of the transporter peptide, e.g., active site, a transmembrane domain or a substrate-binding domain. Further, possible fragments include, but are not limited to, domain or motif containing fragments, soluble peptide fragments, and fragments containing immunogenic structures. Predicted domains and functional sites are readily identifiable by computer programs well known and readily available to those of skill in the art (e.g., PROSITE analysis). The results of one such analysis are provided in FIG. 2 .

Polypeptides often contain amino acids other than the 20 amino acids commonly referred to as the 20 naturally occurring amino acids. Further, many amino acids, including the terminal amino acids, may be modified by natural processes, such as processing and other post-translational modifications, or by chemical modification techniques well known in the art. Common modifications that occur naturally in transporter peptides are described in basic texts, detailed monographs, and the research literature, and they are well known to those of skill in the art (some of these features are identified in FIG. 2 ).

Known modifications include, but are not limited to, acetylation, acylation, ADP-ribosylation, amidation, covalent attachment of flavin, covalent attachment of a heme moiety, covalent attachment of a nucleotide or nucleotide derivative, covalent attachment of a lipid or lipid derivative, covalent attachment of phosphotidylinositol, cross-linking, cyclization, disulfide bond formation, demethylation, formation of covalent crosslinks, formation of cystine, formation of pyroglutamate, formylation, gamma carboxylation, glycosylation, GPI anchor formation, hydroxylation, iodination, methylation, myristoylation, oxidation, proteolytic processing, phosphorylation, prenylation, racemization, selenoylation, sulfation, transfer-RNA mediated addition of amino acids to proteins such as arginylation, and ubiquitination.

Such modifications are well known to those of skill in the art and have been described in great detail in the scientific literature. Several particularly common modifications, glycosylation, lipid attachment, sulfation, gamma-carboxylation of glutamic acid residues, hydroxylation and ADP-ribosylation, for instance, are described in most basic texts, such as Proteins—Structure and Molecular Properties, 2nd Ed., T. E. Creighton, W. H. Freeman and Company, New York (1993). Many detailed reviews are available on this subject, such as by Wold, F., Posttranslational Covalent Modification of Proteins, B. C. Johnson, Ed., Academic Press, New York 1-12 (1983); Seifter et al. ( Meth. Enzymol. 182: 626-646 (1990)) and Rattan et al. ( Ann. N.Y. Acad. Sci. 663:48-62 (1992)).

Accordingly, the transporter peptides of the present invention also encompass derivatives or analogs in which a substituted amino acid residue is not one encoded by the genetic code, in which a substituent group is included, in which the mature transporter peptide is fused with another compound, such as a compound to increase the half-life of the transporter peptide (for example, polyethylene glycol), or in which the additional amino acids are fused to the mature transporter peptide, such as a leader or secretory sequence or a sequence for purification of the mature transporter peptide or a pro-protein sequence.

Protein/Peptide Uses

The proteins of the present invention can be used in substantial and specific assays related to the functional information provided in the Figures; to raise antibodies or to elicit another immune response; as a reagent (including the labeled reagent) in assays designed to quantitatively determine levels of the protein (or its binding partner or ligand) in biological fluids; and as markers for tissues in which the corresponding protein is preferentially expressed (either constitutively or at a particular stage of tissue differentiation or development or in a disease state). Where the protein binds or potentially binds to another protein or ligand (such as, for example, in a transporter-effector protein interaction or transporter-ligand interaction), the protein can be used to identify the binding partner/ligand so as to develop a system to identify inhibitors of the binding interaction. Any or all of these uses are capable of being developed into reagent grade or kit format for commercialization as commercial products.

Methods for performing the uses listed above are well known to those skilled in the art. References disclosing such methods include “Molecular Cloning: A Laboratory Manual”, 2d ed., Cold Spring Harbor Laboratory Press, Sambrook, J., E. F. Fritsch and T. Maniatis eds., 1989, and “Methods in Enzymology: Guide to Molecular Cloning Techniques”, Academic Press, Berger, S. L. and A. R. Kimmel eds., 1987.

The potential uses of the peptides of the present invention are based primarily on the source of the protein as well as the class/action of the protein. For example, transporters isolated from humans and their human/mammalian orthologs serve as targets for identifying agents for use in mammalian therapeutic applications, e.g. a human drug, particularly in modulating a biological or pathological response in a cell or tissue that expresses the transporter. Experimental data as provided in FIG. 1 indicates that the transporter protein of the present invention is expressed in humans in the testis, brain (adult and fetal), placenta, and bone marrow, as indicated by PCR-based tissue screening panels. A large percentage of pharmaceutical agents are being developed that modulate the activity of transporter proteins, particularly members of the sodium bicarbonate cotransporter subfamily (see Background of the Invention). The structural and functional information provided in the Background and Figures provide specific and substantial uses for the molecules of the present invention, particularly in combination with the expression information provided in FIG. 1 . Experimental data as provided in FIG. 1 indicates expression in humans in the testis, brain (adult and fetal), placenta, and bone marrow. Such uses can readily be determined using the information provided herein, that known in the art and routine experimentation.

The proteins of the present invention (including variants and fragments that may have been disclosed prior to the present invention) are useful for biological assays related to transporters that are related to members of the sodium bicarbonate cotransporter subfamily. Such assays involve any of the known transporter functions or activities or properties useful for diagnosis and treatment of transporter-related conditions that are specific for the subfamily of transporters that the one of the present invention belongs to, particularly in cells and tissues that express the transporter. Experimental data as provided in FIG. 1 indicates that the transporter protein of the present invention is expressed in humans in the testis, brain (adult and fetal), placenta, and bone marrow, as indicated by PCR-based tissue screening panels. The proteins of the present invention are also useful in drug screening assays, in cell-based or cell-free systems ((Hodgson, Bio/technology, 1992, September 10(9);973-80). Cell-based systems can be native, i.e., cells that normally express the transporter, as a biopsy or expanded in cell culture. Experimental data as provided in FIG. 1 indicates expression in humans in the testis, brain (adult and fetal), placenta, and bone marrow. In an alternate embodiment, cell-based assays involve recombinant host cells expressing the transporter protein.

The polypeptides can be used to identify compounds that modulate transporter activity of the protein in its natural state or an altered form that causes a specific disease or pathology associated with the transporter. Both the transporters of the present invention and appropriate variants and fragments can be used in high-throughput screens to assay candidate compounds for the ability to bind to the transporter. These compounds can be further screened against a functional transporter to determine the effect of the compound on the transporter activity. Further, these compounds can be tested in animal or invertebrate systems to determine activity/effectiveness. Compounds can be identified that activate (agonist) or inactivate (antagonist) the transporter to a desired degree.

Further, the proteins of the present invention can be used to screen a compound for the ability to stimulate or inhibit interaction between the transporter protein and a molecule that normally interacts with the transporter protein, e.g. a substrate or a component of the signal pathway that the transporter protein normally interacts (for example, another transporter). Such assays typically include the steps of combining the transporter protein with a candidate compound under conditions that allow the transporter protein, or fragment, to interact with the target molecule, and to detect the formation of a complex between the protein and the target or to detect the biochemical consequence of the interaction with the transporter protein and the target, such as any of the associated effects of signal transduction such as changes in membrane potential, protein phosphorylation, cAMP turnover, and adenylate cyclase activation, etc.

Candidate compounds include, for example, 1) peptides such as soluble peptides, including Ig-tailed fusion peptides and members of random peptide libraries (see, e.g., Lam et al., Nature 354:82-84 (1991); Houghten et al., Nature 354:84-86 (1991)) and combinatorial chemistry-derived molecular libraries made of D- and/or L- configuration amino acids; 2) phosphopeptides (e.g., members of random and partially degenerate, directed phosphopeptide libraries, see, e.g., Songyang et al., Cell 72:767-778 (1993)); 3) antibodies (e.g., polyclonal, monoclonal, humanized, anti-idiotypic, chimeric, and single chain antibodies as well as Fab, F(ab′) 2 , Fab expression library fragments, and epitope-binding fragments of antibodies); and 4) small organic and inorganic molecules (e.g., molecules obtained from combinatorial and natural product libraries).

One candidate compound is a soluble fragment of the receptor that competes for ligand binding. Other candidate compounds include mutant transporters or appropriate fragments containing mutations that affect transporter function and thus compete for ligand. Accordingly, a fragment that competes for ligand, for example with a higher affinity, or a fragment that binds ligand but does not allow release, is encompassed by the invention.

The invention further includes other end point assays to identify compounds that modulate (stimulate or inhibit) transporter activity. The assays typically involve an assay of events in the signal transduction pathway that indicate transporter activity. Thus, the transport of a ligand, change in cell membrane potential, activation of a protein, a change in the expression of genes that are up- or down-regulated in response to the transporter protein dependent signal cascade can be assayed.

Any of the biological or biochemical functions mediated by the transporter can be used as an endpoint assay. These include all of the biochemical or biochemical/biological events described herein, in the references cited herein, incorporated by reference for these endpoint assay targets, and other functions known to those of ordinary skill in the art or that can be readily identified using the information provided in the Figures, particularly FIG. 2 . Specifically, a biological function of a cell or tissues that expresses the transporter can be assayed. Experimental data as provided in FIG. 1 indicates that the transporter protein of the present invention is expressed in humans in the testis, brain (adult and fetal), placenta, and bone marrow, as indicated by PCR-based tissue screening panels.

Binding and/or activating compounds can also be screened by using chimeric transporter proteins in which the amino terminal extracellular domain, or parts thereof, the entire transmembrane domain or subregions, such as any of the seven transmembrane segments or any of the intracellular or extracellular loops and the carboxy terminal intracellular domain, or parts thereof, can be replaced by heterologous domains or subregions. For example, a ligand-binding region can be used that interacts with a different ligand then that which is recognized by the native transporter. Accordingly, a different set of signal transduction components is available as an end-point assay for activation. This allows for assays to be performed in other than the specific host cell from which the transporter is derived.

The proteins of the present invention are also useful in competition binding assays in methods designed to discover compounds that interact with the transporter (e.g. binding partners and/or ligands). Thus, a compound is exposed to a transporter polypeptide under conditions that allow the compound to bind or to otherwise interact with the polypeptide. Soluble transporter polypeptide is also added to the mixture. If the test compound interacts with the soluble transporter polypeptide, it decreases the amount of complex formed or activity from the transporter target. This type of assay is particularly useful in cases in which compounds are sought that interact with specific regions of the transporter. Thus, the soluble polypeptide that competes with the target transporter region is designed to contain peptide sequences corresponding to the region of interest.

To perform cell free drug screening assays, it is sometimes desirable to immobilize either the transporter protein, or fragment, or its target molecule to facilitate separation of complexes from uncomplexed forms of one or both of the proteins, as well as to accommodate automation of the assay.

Techniques for immobilizing proteins on matrices can be used in the drug screening assays. In one embodiment, a fusion protein can be provided which adds a domain that allows the protein to be bound to a matrix. For example, glutathione-S-transferase fusion proteins can be adsorbed onto glutathione sepharose beads (Sigma Chemical, St. Louis, Mo.) or glutathione derivatized microtitre plates, which are then combined with the cell lysates (e.g., 35 S-labeled) and the candidate compound, and the mixture incubated under conditions conducive to complex formation (e.g., at physiological conditions for salt and pH). Following incubation, the beads are washed to remove any unbound label, and the matrix immobilized and radiolabel determined directly, or in the supernatant after the complexes are dissociated. Alternatively, the complexes can be dissociated from the matrix, separated by SDS-PAGE, and the level of transporter-binding protein found in the bead fraction quantitated from the gel using standard electrophoretic techniques. For example, either the polypeptide or its target molecule can be immobilized utilizing conjugation of biotin and streptavidin using techniques well known in the art. Alternatively, antibodies reactive with the protein but which do not interfere with binding of the protein to its target molecule can be derivatized to the wells of the plate, and the protein trapped in the wells by antibody conjugation. Preparations of a transporter-binding protein and a candidate compound are incubated in the transporter protein-presenting wells and the amount of complex trapped in the well can be quantitated. Methods for detecting such complexes, in addition to those described above for the GST-immobilized complexes, include immunodetection of complexes using antibodies reactive with the transporter protein target molecule, or which are reactive with transporter protein and compete with the target molecule, as well as enzyme-linked assays which rely on detecting an enzymatic activity associated with the target molecule.

Agents that modulate one of the transporters of the present invention can be identified using one or more of the above assays, alone or in combination. It is generally preferable to use a cell-based or cell free system first and then confirm activity in an animal or other model system. Such model systems are well known in the art and can readily be employed in this context.

Modulators of transporter protein activity identified according to these drug screening assays can be used to treat a subject with a disorder mediated by the transporter pathway, by treating cells or tissues that express the transporter. Experimental data as provided in FIG. 1 indicates expression in humans in the testis, brain (adult and fetal), placenta, and bone marrow. These methods of treatment include the steps of administering a modulator of transporter activity in a pharmaceutical composition to a subject in need of such treatment, the modulator being identified as described herein.

In yet another aspect of the invention, the transporter proteins can be used as “bait proteins” in a two-hybrid assay or three-hybrid assay (see, e.g., U.S. Pat. No. 5,283,317; Zervos et al (1993) Cell 72:223-232; Madura et al. (1993) J. Biol. Chem. 268:12046-12054; Bartel et al. (1993) Biotechniques 14:920-924; Iwabuchi et al. (1993) Oncogene 8:1693-1696; and Brent WO94/10300), to identify other proteins, which bind to or interact with the transporter and are involved in transporter activity. Such transporter-binding proteins are also likely to be involved in the propagation of signals by the transporter proteins or transporter targets as, for example, downstream elements of a transporter-mediated signaling pathway. Alternatively, such transporter-binding proteins are likely to be transporter inhibitors.

The two-hybrid system is based on the modular nature of most transcription factors, which consist of separable DNA-binding and activation domains. Briefly, the assay utilizes two different DNA constructs. In one construct, the gene that codes for a transporter protein is fused to a gene encoding the DNA binding domain of a known transcription factor (e.g., GAL-4). In the other construct, a DNA sequence, from a library of DNA sequences, that encodes an unidentified protein (“prey” or “sample”) is fused to a gene that codes for the activation domain of the known transcription factor. If the “bait” and the “prey” proteins are able to interact, in vivo, forming a transporter-dependent complex, the DNA-binding and activation domains of the transcription factor are brought into close proximity. This proximity allows transcription of a reporter gene (e.g., LacZ) which is operably linked to a transcriptional regulatory site responsive to the transcription factor. Expression of the reporter gene can be detected and cell colonies containing the functional transcription factor can be isolated and used to obtain the cloned gene which encodes the protein which interacts with the transporter protein.

This invention further pertains to novel agents identified by the above-described screening assays. Accordingly, it is within the scope of this invention to further use an agent identified as described herein in an appropriate animal model. For example, an agent identified as described herein (e.g., a transporter-modulating agent, an antisense transporter nucleic acid molecule, a transporter-specific antibody, or a transporter-binding partner) can be used in an animal or other model to determine the efficacy, toxicity, or side effects of treatment with such an agent. Alternatively, an agent identified as described herein can be used in an animal or other model to determine the mechanism of action of such an agent. Furthermore, this invention pertains to uses of novel agents identified by the above-described screening assays for treatments as described herein.

The transporter proteins of the present invention are also useful to provide a target for diagnosing a disease or predisposition to disease mediated by the peptide. Accordingly, the invention provides methods for detecting the presence, or levels of, the protein (or encoding mRNA) in a cell, tissue, or organism. Experimental data as provided in FIG. 1 indicates expression in humans in the testis, brain (adult and fetal), placenta, and bone marrow. The method involves contacting a biological sample with a compound capable of interacting with the transporter protein such that the interaction can be detected. Such an assay can be provided in a single detection format or a multi-detection format such as an antibody chip array.

One agent for detecting a protein in a sample is an antibody capable of selectively binding to protein. A biological sample includes tissues, cells and biological fluids isolated from a subject, as well as tissues, cells and fluids present within a subject.

The peptides of the present invention also provide targets for diagnosing active protein activity, disease, or predisposition to disease, in a patient having a variant peptide, particularly activities and conditions that are known for other members of the family of proteins to which the present one belongs. Thus, the peptide can be isolated from a biological sample and assayed for the presence of a genetic mutation that results in aberrant peptide. This includes amino acid substitution, deletion, insertion, rearrangement, (as the result of aberrant splicing events), and inappropriate post-translational modification. Analytic methods include altered electrophoretic mobility, altered tryptic peptide digest, altered transporter activity in cell-based or cell-free assay, alteration in ligand or antibody-binding pattern, altered isoelectric point, direct amino acid sequencing, and any other of the known assay techniques useful for detecting mutations in a protein. Such an assay can be provided in a single detection format or a multi-detection format such as an antibody chip array.

In vitro techniques for detection of peptide include enzyme linked immunosorbent assays (ELISAs), Western blots, immunoprecipitations and immunofluorescence using a detection reagent, such as an antibody or protein binding agent. Alternatively, the peptide can be detected in vivo in a subject by introducing into the subject a labeled anti-peptide antibody or other types of detection agent. For example, the antibody can be labeled with a radioactive marker whose presence and location in a subject can be detected by standard imaging techniques. Particularly useful are methods that detect the allelic variant of a peptide expressed in a subject and methods which detect fragments of a peptide in a sample.

The peptides are also useful in pharmacogenomic analysis. Pharmacogenomics deal with clinically significant hereditary variations in the response to drugs due to altered drug disposition and abnormal action in affected persons. See, e.g., Eichelbaum, M. ( Clin. Exp. Pharmacol. Physiol. 23(10-11):983-985 (1996)), and Linder, M. W. ( Clin. Chem. 43(2):254-266 (1997)). The clinical outcomes of these variations result in severe toxicity of therapeutic drugs in certain individuals or therapeutic failure of drugs in certain individuals as a result of individual variation in metabolism. Thus, the genotype of the individual can determine the way a therapeutic compound acts on the body or the way the body metabolizes the compound. Further, the activity of drug metabolizing enzymes effects both the intensity and duration of drug action. Thus, the pharmacogenomics of the individual permit the selection of effective compounds and effective dosages of such compounds for prophylactic or therapeutic treatment based on the individual's genotype. The discovery of genetic polymorphisms in some drug metabolizing enzymes has explained why some patients do not obtain the expected drug effects, show an exaggerated drug effect, or experience serious toxicity from standard drug dosages. Polymorphisms can be expressed in the phenotype of the extensive metabolizer and the phenotype of the poor metabolizer. Accordingly, genetic polymorphism may lead to allelic protein variants of the transporter protein in which one or more of the transporter functions in one population is different from those in another population. The peptides thus allow a target to ascertain a genetic predisposition that can affect treatment modality. Thus, in a ligand-based treatment, polymorphism may give rise to amino terminal extracellular domains and/or other ligand-binding regions that are more or less active in ligand binding, and transporter activation. Accordingly, ligand dosage would necessarily be modified to maximize the therapeutic effect within a given population containing a polymorphism. As an alternative to genotyping, specific polymorphic peptides could be identified.

The peptides are also useful for treating a disorder characterized by an absence of, inappropriate, or unwanted expression of the protein. Experimental data as provided in FIG. 1 indicates expression in humans in the testis, brain (adult and fetal), placenta, and bone marrow. Accordingly, methods for treatment include the use of the transporter protein or fragments.

Antibodies

The invention also provides antibodies that selectively bind to one of the peptides of the present invention, a protein comprising such a peptide, as well as variants and fragments thereof. As used herein, an antibody selectively binds a target peptide when it binds the target peptide and does not significantly bind to unrelated proteins. An antibody is still considered to selectively bind a peptide even if it also binds to other proteins that are not substantially homologous with the target peptide so long as such proteins share homology with a fragment or domain of the peptide target of the antibody. In this case, it would be understood that antibody binding to the peptide is still selective despite some degree of cross-reactivity.

As used herein, an antibody is defined in terms consistent with that recognized within the art: they are multi-subunit proteins produced by a mammalian organism in response to an antigen challenge. The antibodies of the present invention include polyclonal antibodies and monoclonal antibodies, as well as fragments of such antibodies, including, but not limited to, Fab or F(ab′) 2 , and Fv fragments.

Many methods are known for generating and/or identifying antibodies to a given target peptide. Several such methods are described by Harlow, Antibodies, Cold Spring Harbor Press, (1989).

In general, to generate antibodies, an isolated peptide is used as an immunogen and is administered to a mammalian organism, such as a rat, rabbit or mouse. The full-length protein, an antigenic peptide fragment or a fusion protein can be used. Particularly important fragments are those covering functional domains, such as the domains identified in FIG. 2, and domain of sequence homology or divergence amongst the family, such as those that can readily be identified using protein alignment methods and as presented in the Figures.

Antibodies are preferably prepared from regions or discrete fragments of the transporter proteins. Antibodies can be prepared from any region of the peptide as described herein. However, preferred regions will include those involved in function/activity and/or transporter/binding partner interaction. FIG. 2 can be used to identify particularly important regions while sequence alignment can be used to identify conserved and unique sequence fragments.

An antigenic fragment will typically comprise at least 8 contiguous amino acid residues. The antigenic peptide can comprise, however, at least 10, 12, 14, 16 or more amino acid residues. Such fragments can be selected on a physical property, such as fragments correspond to regions that are located on the surface of the protein, e.g., hydrophilic regions or can be selected based on sequence uniqueness (see FIG. 2 ).

Detection on an antibody of the present invention can be facilitated by coupling (i.e., physically linking) the antibody to a detectable substance. Examples of detectable substances include various enzymes, prosthetic groups, fluorescent materials, luminescent materials, bioluminescent materials, and radioactive materials. Examples of suitable enzymes include horseradish peroxidase, alkaline phosphatase, β-galactosidase, or acetylcholinesterase; examples of suitable prosthetic group complexes include streptavidin/biotin and avidin/biotin; examples of suitable fluorescent materials include umbelliferone, fluorescein, fluorescein isothiocyanate, rhodamine, dichlorotriazinylamine fluorescein, dansyl chloride or phycoerythrin; an example of a luminescent material includes luminol; examples of bioluminescent materials include luciferase, luciferin, and aequorin, and examples of suitable radioactive material include 125 I, 131 I, 35 S or 3 H.

Antibody Uses

The antibodies can be used to isolate one of the proteins of the present invention by standard techniques, such as affinity chromatography or immunoprecipitation. The antibodies can facilitate the purification of the natural protein from cells and recombinantly produced protein expressed in host cells. In addition, such antibodies are useful to detect the presence of one of the proteins of the present invention in cells or tissues to determine the pattern of expression of the protein among various tissues in an organism and over the course of normal development. Experimental data as provided in FIG. 1 indicates that the transporter protein of the present invention is expressed in humans in the testis, brain (adult and fetal), placenta, and bone marrow, as indicated by PCR-based tissue screening panels. Further, such antibodies can be used to detect protein in situ, in vitro, or in a cell lysate or supernatant in order to evaluate the abundance and pattern of expression. Also, such antibodies can be used to assess abnormal tissue distribution or abnormal expression during development or progression of a biological condition. Antibody detection of circulating fragments of the full length protein can be used to identify turnover.

Further, the antibodies can be used to assess expression in disease states such as in active stages of the disease or in an individual with a predisposition toward disease related to the protein's function. When a disorder is caused by an inappropriate tissue distribution, developmental expression, level of expression of the protein, or expressed/processed form, the antibody can be prepared against the normal protein. Experimental data as provided in FIG. 1 indicates expression in humans in the testis, brain (adult and fetal), placenta, and bone marrow. If a disorder is characterized by a specific mutation in the protein, antibodies specific for this mutant protein can be used to assay for the presence of the specific mutant protein.

The antibodies can also be used to assess normal and aberrant subcellular localization of cells in the various tissues in an organism. Experimental data as provided in FIG. 1 indicates expression in humans in the testis, brain (adult and fetal), placenta, and bone marrow. The diagnostic uses can be applied, not only in genetic testing, but also in monitoring a treatment modality. Accordingly, where treatment is ultimately aimed at correcting expression level or the presence of aberrant sequence and aberrant tissue distribution or developmental expression, antibodies directed against the protein or relevant fragments can be used to monitor therapeutic efficacy.

Additionally, antibodies are useful in pharmacogenomic analysis. Thus, antibodies prepared against polymorphic proteins can be used to identify individuals that require modified treatment modalities. The antibodies are also useful as diagnostic tools as an immunological marker for aberrant protein analyzed by electrophoretic mobility, isoelectric point, tryptic peptide digest, and other physical assays known to those in the art.

The antibodies are also useful for tissue typing. Experimental data as provided in FIG. 1 indicates expression in humans in the testis, brain (adult and fetal), placenta, and bone marrow. Thus, where a specific protein has been correlated with expression in a specific tissue, antibodies that are specific for this protein can be used to identify a tissue type.

The antibodies are also useful for inhibiting protein function, for example, blocking the binding of the transporter peptide to a binding partner such as a ligand or protein binding partner. These uses can also be applied in a therapeutic context in which treatment involves inhibiting the protein's function. An antibody can be used, for example, to block binding, thus modulating (agonizing or antagonizing) the peptides activity. Antibodies can be prepared against specific fragments containing sites required for function or against intact protein that is associated with a cell or cell membrane. See FIG. 2 for structural information relating to the proteins of the present invention.

The invention also encompasses kits for using antibodies to detect the presence of a protein in a biological sample. The kit can comprise antibodies such as a labeled or labelable antibody and a compound or agent for detecting protein in a biological sample; means for determining the amount of protein in the sample; means for comparing the amount of protein in the sample with a standard; and instructions for use. Such a kit can be supplied to detect a single protein or epitope or can be configured to detect one of a multitude of epitopes, such as in an antibody detection array. Arrays are described in detail below for nucleic acid arrays and similar methods have been developed for antibody arrays.

Nucleic Acid Molecules

The present invention further provides isolated nucleic acid molecules that encode a transporter peptide or protein of the present invention (cDNA, transcript and genomic sequence). Such nucleic acid molecules will consist of, consist essentially of, or comprise a nucleotide sequence that encodes one of the transporter peptides of the present invention, an allelic variant thereof, or an ortholog or paralog thereof.

As used herein, an “isolated” nucleic acid molecule is one that is separated from other nucleic acid present in the natural source of the nucleic acid. Preferably, an “isolated” nucleic acid is free of sequences that naturally flank the nucleic acid (i.e., sequences located at the 5′ and 3′ ends of the nucleic acid) in the genomic DNA of the organism from which the nucleic acid is derived. However, there can be some flanking nucleotide sequences, for example up to about 5 KB, 4 KB, 3 KB, 2 KB, or 1 KB or less, particularly contiguous peptide encoding sequences and peptide encoding sequences within the same gene but separated by introns in the genomic sequence. The important point is that the nucleic acid is isolated from remote and unimportant flanking sequences such that it can be subjected to the specific manipulations described herein such as recombinant expression, preparation of probes and primers, and other uses specific to the nucleic acid sequences.

Moreover, an “isolated” nucleic acid molecule, such as a transcript/cDNA molecule, can be substantially free of other cellular material, or culture medium when produced by recombinant techniques, or chemical precursors or other chemicals when chemically synthesized. However, the nucleic acid molecule can be fused to other coding or regulatory sequences and still be considered isolated.

For example, recombinant DNA molecules contained in a vector are considered isolated. Further examples of isolated DNA molecules include recombinant DNA molecules maintained in heterologous host cells or purified (partially or substantially) DNA molecules in solution. Isolated RNA molecules include in vivo or in vitro RNA transcripts of the isolated DNA molecules of the present invention. Isolated nucleic acid molecules according to the present invention further include such molecules produced synthetically.

Accordingly, the present invention provides nucleic acid molecules that consist of the nucleotide sequence shown in FIG. 1 or 3 (SEQ ID NO: 1, transcript sequence and SEQ ID NO:3, genomic sequence), or any nucleic acid molecule that encodes the protein provided in FIG. 2, SEQ ID NO:2. A nucleic acid molecule consists of a nucleotide sequence when the nucleotide sequence is the complete nucleotide sequence of the nucleic acid molecule.

The present invention further provides nucleic acid molecules that consist essentially of the nucleotide sequence shown in FIG. 1 or 3 (SEQ ID NO:1, transcript sequence and SEQ ID NO:3, genomic sequence), or any nucleic acid molecule that encodes the protein provided in FIG. 2, SEQ ID NO:2. A nucleic acid molecule consists essentially of a nucleotide sequence when such a nucleotide sequence is present with only a few additional nucleic acid residues in the final nucleic acid molecule.

The present invention further provides nucleic acid molecules that comprise the nucleotide sequences shown in FIG. 1 or 3 (SEQ ID NO:1, transcript sequence and SEQ ID NO:3, genomic sequence), or any nucleic acid molecule that encodes the protein provided in FIG. 2, SEQ ID NO:2. A nucleic acid molecule comprises a nucleotide sequence when the nucleotide sequence is at least part of the final nucleotide sequence of the nucleic acid molecule. In such a fashion, the nucleic acid molecule can be only the nucleotide sequence or have additional nucleic acid residues, such as nucleic acid residues that are naturally associated with it or heterologous nucleotide sequences. Such a nucleic acid molecule can have a few additional nucleotides or can comprise several hundred or more additional nucleotides. A brief description of how various types of these nucleic acid molecules can be readily made/isolated is provided below.

In FIGS. 1 and 3, both coding and non-coding sequences are provided. Because of the source of the present invention, humans genomic sequence (FIG. 3) and cDNA/transcript sequences (FIG. 1 ), the nucleic acid molecules in the Figures will contain genomic intronic sequences, 5′ and 3′ non-coding sequences, gene regulatory regions and non-coding intergenic sequences. In general such sequence features are either noted in FIGS. 1 and 3 or can readily be identified using computational tools known in the art. As discussed below, some of the non-coding regions, particularly gene regulatory elements such as promoters, are useful for a variety of purposes, e.g. control of heterologous gene expression, target for identifying gene activity modulating compounds, and are particularly claimed as fragments of the genomic sequence provided herein.

The isolated nucleic acid molecules can encode the mature protein plus additional amino or carboxyl-terminal amino acids, or amino acids interior to the mature peptide (when the mature form has more than one peptide chain, for instance). Such sequences may play a role in processing of a protein from precursor to a mature form, facilitate protein trafficking, prolong or shorten protein half-life or facilitate manipulation of a protein for assay or production, among other things. As generally is the case in situ, the additional amino acids may be processed away from the mature protein by cellular enzymes.

As mentioned above, the isolated nucleic acid molecules include, but are not limited to, the sequence encoding the transporter peptide alone, the sequence encoding the mature peptide and additional coding sequences, such as a leader or secretory sequence (e.g., a pre-pro or pro-protein sequence), the sequence encoding the mature peptide, with or without the additional coding sequences, plus additional non-coding sequences, for example introns and non-coding 5′ and 3′ sequences such as transcribed but non-translated sequences that play a role in transcription, mRNA processing (including splicing and polyadenylation signals), ribosome binding and stability of mRNA. In addition, the nucleic acid molecule may be fused to a marker sequence encoding, for example, a peptide that facilitates purification.

Isolated nucleic acid molecules can be in the form of RNA, such as mRNA, or in the form DNA, including cDNA and genomic DNA obtained by cloning or produced by chemical synthetic techniques or by a combination thereof. The nucleic acid, especially DNA, can be double-stranded or single-stranded. Single-stranded nucleic acid can be the coding strand (sense strand) or the non-coding strand (anti-sense strand).

The invention further provides nucleic acid molecules that encode fragments of the peptides of the present invention as well as nucleic acid molecules that encode obvious variants of the transporter proteins of the present invention that are described above. Such nucleic acid molecules may be naturally occurring, such as allelic variants (same locus), paralogs (different locus), and orthologs (different organism), or may be constructed by recombinant DNA methods or by chemical synthesis. Such non-naturally occurring variants may be made by mutagenesis techniques, including those applied to nucleic acid molecules, cells, or organisms. Accordingly, as discussed above, the variants can contain nucleotide substitutions, deletions, inversions and insertions. Variation can occur in either or both the coding and non-coding regions. The variations can produce both conservative and non-conservative amino acid substitutions.

The present invention further provides non-coding fragments of the nucleic acid molecules provided in FIGS. 1 and 3. Preferred non-coding fragments include, but are not limited to, promoter sequences, enhancer sequences, gene modulating sequences and gene termination sequences. Such fragments are useful in controlling heterologous gene expression and in developing screens to identify gene-modulating agents. A promoter can readily be identified as being 5′ to the ATG start site in the genomic sequence provided in FIG. 3 .

A fragment comprises a contiguous nucleotide sequence greater than 12 or more nucleotides. Further, a fragment could at least 30, 40, 50, 100, 250 or 500 nucleotides in length. The length of the fragment will be based on its intended use. For example, the fragment can encode epitope bearing regions of the peptide, or can be useful as DNA probes and primers. Such fragments can be isolated using the known nucleotide sequence to synthesize an oligonucleotide probe. A labeled probe can then be used to screen a cDNA library, genomic DNA library, or mRNA to isolate nucleic acid corresponding to the coding region. Further, primers can be used in PCR reactions to clone specific regions of gene.

A probe/primer typically comprises substantially a purified oligonucleotide or oligonucleotide pair. The oligonucleotide typically comprises a region of nucleotide sequence that hybridizes under stringent conditions to at least about 12, 20, 25, 40, 50 or more consecutive nucleotides.

Orthologs, homologs, and allelic variants can be identified using methods well known in the art. As described in the Peptide Section, these variants comprise a nucleotide sequence encoding a peptide that is typically 60-70%, 70-80%, 80-90%, and more typically at least about 90-95% or more homologous to the nucleotide sequence shown in the Figure sheets or a fragment of this sequence. Such nucleic acid molecules can readily be identified as being able to hybridize under moderate to stringent conditions, to the nucleotide sequence shown in the Figure sheets or a fragment of the sequence. Allelic variants can readily be determined by genetic locus of the encoding gene. As indicated by the data presented in FIG. 3, the gene provided by the present invention is located on public BAC AC008063.2, which is known to be mapped to chromosome 2.

FIG. 3 provides information on SNPs that have been found in the gene encoding the transporter protein of the present invention. SNPs, including insertion/deletion polymorphisms (“indels”), were identifed at 87 different nucleotide positions. Changes in the amino acid sequence caused by these SNPs can readily be determined using the universal genetic code and the protein sequence provided in FIG. 2 as a reference. SNPs outside the ORF and in introns may affect control/regulatory elements. SNP positioning in exons, introns, or outside the ORF can readily be determined based on the genomic features given in FIG. 3 .

As used herein, the term “hybridizes under stringent conditions” is intended to describe conditions for hybridization and washing under which nucleotide sequences encoding a peptide at least 60-70% homologous to each other typically remain hybridized to each other. The conditions can be such that sequences at least about 60%, at least about 70%, or at least about 80% or more homologous to each other typically remain hybridized to each other. Such stringent conditions are known to those skilled in the art and can be found in Current Protocols in Molecular Biology, John Wiley & Sons, New York (1989), 6.3.1-6.3.6. One example of stringent hybridization conditions are hybridization in 6× sodium chloride/sodium citrate (SSC) at about 45 C, followed by one or more washes in 0.2× SSC, 0.1% SDS at 50-65 C. Examples of moderate to low stringency hybridization conditions are well known in the art.

Nucleic Acid Molecule Uses

The nucleic acid molecules of the present invention are useful for probes, primers, chemical intermediates, and in biological assays. The nucleic acid molecules are useful as a hybridization probe for messenger RNA, transcript/cDNA and genomic DNA to isolate full-length cDNA and genomic clones encoding the peptide described in FIG. 2 and to isolate cDNA and genomic clones that correspond to variants (alleles, orthologs, etc.) producing the same or related peptides shown in FIG. 2 . As illustrated in FIG. 3, SNPs, including insertion/deletion polymorphisms (“indels”), were identifed at 87 different nucleotide positions.

The probe can correspond to any sequence along the entire length of the nucleic acid molecules provided in the Figures. Accordingly, it could be derived from 5′ noncoding regions, the coding region, and 3′ noncoding regions. However, as discussed, fragments are not to be construed as encompassing fragments disclosed prior to the present invention.

The nucleic acid molecules are also useful as primers for PCR to amplify any given region of a nucleic acid molecule and are useful to synthesize antisense molecules of desired length and sequence.

The nucleic acid molecules are also useful for constructing recombinant vectors. Such vectors include expression vectors that express a portion of, or all of, the peptide sequences. Vectors also include insertion vectors, used to integrate into another nucleic acid molecule sequence, such as into the cellular genome, to alter in situ expression of a gene and/or gene product. For example, an endogenous coding sequence can be replaced via homologous recombination with all or part of the coding region containing one or more specifically introduced mutations.

The nucleic acid molecules are also useful for expressing antigenic portions of the proteins.

The nucleic acid molecules are also useful as probes for determining the chromosomal positions of the nucleic acid molecules by means of in situ hybridization methods. As indicated by the data presented in FIG. 3, the gene provided by the present invention is located on public BAC AC008063.2, which is known to be mapped to chromosome 2.

The nucleic acid molecules are also useful in making vectors containing the gene regulatory regions of the nucleic acid molecules of the present invention.

The nucleic acid molecules are also useful for designing ribozymes corresponding to all, or a part, of the mRNA produced from the nucleic acid molecules described herein.

The nucleic acid molecules are also useful for making vectors that express part, or all, of the peptides.

The nucleic acid molecules are also useful for constructing host cells expressing a part, or all, of the nucleic acid molecules and peptides.

The nucleic acid molecules are also useful for constructing transgenic animals expressing all, or a part, of the nucleic acid molecules and peptides.

The nucleic acid molecules are also useful as hybridization probes for determining the presence, level, form and distribution of nucleic acid expression. Experimental data as provided in FIG. 1 indicates that the transporter protein of the present invention is expressed in humans in the testis, brain (adult and fetal), placenta, and bone marrow, as indicated by PCR-based tissue screening panels.

Accordingly, the probes can be used to detect the presence of, or to determine levels of, a specific nucleic acid molecule in cells, tissues, and in organisms. The nucleic acid whose level is determined can be DNA or RNA. Accordingly, probes corresponding to the peptides described herein can be used to assess expression and/or gene copy number in a given cell, tissue, or organism. These uses are relevant for diagnosis of disorders involving an increase or decrease in transporter protein expression relative to normal results.

In vitro techniques for detection of mRNA include Northern hybridizations and in situ hybridizations. In vitro techniques for detecting DNA include Southern hybridizations and in situ hybridization.

Probes can be used as a part of a diagnostic test kit for identifying cells or tissues that express a transporter protein, such as by measuring a level of a transporter-encoding nucleic acid in a sample of cells from a subject e.g., mRNA or genomic DNA, or determining if a transporter gene has been mutated. Experimental data as provided in FIG. 1 indicates that the transporter protein of the present invention is expressed in humans in the testis, brain (adult and fetal), placenta, and bone marrow, as indicated by PCR-based tissue screening panels.

Nucleic acid expression assays are useful for drug screening to identify compounds that modulate transporter nucleic acid expression.

The invention thus provides a method for identifying a compound that can be used to treat a disorder associated with nucleic acid expression of the transporter gene, particularly biological and pathological processes that are mediated by the transporter in cells and tissues that express it. Experimental data as provided in FIG. 1 indicates expression in humans in the testis, brain (adult and fetal), placenta, and bone marrow. The method typically includes assaying the ability of the compound to modulate the expression of the transporter nucleic acid and thus identifying a compound that can be used to treat a disorder characterized by undesired transporter nucleic acid expression. The assays can be performed in cell-based and cell-free systems. Cell-based assays include cells naturally expressing the transporter nucleic acid or recombinant cells genetically engineered to express specific nucleic acid sequences.

The assay for transporter nucleic acid expression can involve direct assay of nucleic acid levels, such as mRNA levels, or on collateral compounds involved in the signal pathway. Further, the expression of genes that are up- or down-regulated in response to the transporter protein signal pathway can also be assayed. In this embodiment the regulatory regions of these genes can be operably linked to a reporter gene such as luciferase.

Thus, modulators of transporter gene expression can be identified in a method wherein a cell is contacted with a candidate compound and the expression of mRNA determined. The level of expression of transporter mRNA in the presence of the candidate compound is compared to the level of expression of transporter mRNA in the absence of the candidate compound. The candidate compound can then be identified as a modulator of nucleic acid expression based on this comparison and be used, for example to treat a disorder characterized by aberrant nucleic acid expression. When expression of mRNA is statistically significantly greater in the presence of the candidate compound than in its absence, the candidate compound is identified as a stimulator of nucleic acid expression. When nucleic acid expression is statistically significantly less in the presence of the candidate compound than in its absence, the candidate compound is identified as an inhibitor of nucleic acid expression.

The invention further provides methods of treatment, with the nucleic acid as a target, using a compound identified through drug screening as a gene modulator to modulate transporter nucleic acid expression in cells and tissues that express the transporter. Experimental data as provided in FIG. 1 indicates that the transporter protein of the present invention is expressed in humans in the testis, brain (adult and fetal), placenta, and bone marrow, as indicated by PCR-based tissue screening panels. Modulation includes both up-regulation (i.e. activation or agonization) or down-regulation (suppression or antagonization) or nucleic acid expression.

Alternatively, a modulator for transporter nucleic acid expression can be a small molecule or drug identified using the screening assays described herein as long as the drug or small molecule inhibits the transporter nucleic acid expression in the cells and tissues that express the protein. Experimental data as provided in FIG. 1 indicates expression in humans in the testis, brain (adult and fetal), placenta, and bone marrow.

The nucleic acid molecules are also useful for monitoring the effectiveness of modulating compounds on the expression or activity of the transporter gene in clinical trials or in a treatment regimen. Thus, the gene expression pattern can serve as a barometer for the continuing effectiveness of treatment with the compound, particularly with compounds to which a patient can develop resistance. The gene expression pattern can also serve as a marker indicative of a physiological response of the affected cells to the compound. Accordingly, such monitoring would allow either increased administration of the compound or the administration of alternative compounds to which the patient has not become resistant. Similarly, if the level of nucleic acid expression falls below a desirable level, administration of the compound could be commensurately decreased.

The nucleic acid molecules are also useful in diagnostic assays for qualitative changes in transporter nucleic acid expression, and particularly in qualitative changes that lead to pathology. The nucleic acid molecules can be used to detect mutations in transporter genes and gene expression products such as mRNA. The nucleic acid molecules can be used as hybridization probes to detect naturally occurring genetic mutations in the transporter gene and thereby to determine whether a subject with the mutation is at risk for a disorder caused by the mutation. Mutations include deletion, addition, or substitution of one or more nucleotides in the gene, chromosomal rearrangement, such as inversion or transposition, modification of genomic DNA, such as aberrant methylation patterns or changes in gene copy number, such as amplification. Detection of a mutated form of the transporter gene associated with a dysfunction provides a diagnostic tool for an active disease or susceptibility to disease when the disease results from overexpression, underexpression, or altered expression of a transporter protein.

Individuals carrying mutations in the transporter gene can be detected at the nucleic acid level by a variety of techniques. FIG. 3 provides information on SNPs that have been found in the gene encoding the transporter protein of the present invention. SNPs, including insertion/deletion polymorphisms (“indels”), were identifed at 87 different nucleotide positions. Changes in the amino acid sequence caused by these SNPs can readily be determined using the universal genetic code and the protein sequence provided in FIG. 2 as a reference. SNPs outside the ORF and in introns may affect control/regulatory elements. SNP positioning in exons, introns, or outside the ORF can readily be determined based on the genomic features given in FIG. 3 . As indicated by the data presented in FIG. 3, the gene provided by the present invention is located on public BAC AC008063.2, which is known to be mapped to chromosome 2. Genomic DNA can be analyzed directly or can be amplified by using PCR prior to analysis. RNA or cDNA can be used in the same way. In some uses, detection of the mutation involves the use of a probe/primer in a polymerase chain reaction (PCR) (see, e.g. U.S. Pat. Nos. 4,683,195 and 4,683,202), such as anchor PCR or RACE PCR, or, alternatively, in a ligation chain reaction (LCR) (see, e.g., Landegran et al., Science 241:1077-1080 (1988); and Nakazawa et al., PNAS 91:360-364 (1994)), the latter of which can be particularly useful for detecting point mutations in the gene (see Abravaya et al, Nucleic Acids Res. 23:675-682 (1995)). This method can include the steps of collecting a sample of cells from a patient, isolating nucleic acid (e.g., genomic, mRNA or both) from the cells of the sample, contacting the nucleic acid sample with one or more primers which specifically hybridize to a gene under conditions such that hybridization and amplification of the gene (if present) occurs, and detecting the presence or absence of an amplification product, or detecting the size of the amplification product and comparing the length to a control sample. Deletions and insertions can be detected by a change in size of the amplified product compared to the normal genotype. Point mutations can be identified by hybridizing amplified DNA to normal RNA or antisense DNA sequences.

Alternatively, mutations in a transporter gene can be directly identified, for example, by alterations in restriction enzyme digestion patterns determined by gel electrophoresis.

Further, sequence-specific ribozymes (U.S. Pat. No. 5,498,531) can be used to score for the presence of specific mutations by development or loss of a ribozyme cleavage site. Perfectly matched sequences can be distinguished from mismatched sequences by nuclease cleavage digestion assays or by differences in melting temperature.

Sequence changes at specific locations can also be assessed by nuclease protection assays such as RNase and S1 protection or the chemical cleavage method. Furthermore, sequence differences between a mutant transporter gene and a wild-type gene can be determined by direct DNA sequencing. A variety of automated sequencing procedures can be utilized when performing the diagnostic assays (Naeve, C. W., (1995) Biotechniques 19:448), including sequencing by mass spectrometry (see, e.g., PCT International Publication No. WO 94/16101; Cohen et al., Adv. Chromatogr. 36:127-162 (1996); and Griffin et al, Appl. Biochem. Biotechnol. 38:147-159 (1993)).

Other methods for detecting mutations in the gene include methods in which protection from cleavage agents is used to detect mismatched bases in RNA/RNA or RNA/DNA duplexes (Myers et al., Science 230:1242 (1985)); Cotton et al., PNAS 85:4397 (1988); Saleeba et al., Meth. Enzymol. 217:286-295 (1992)), electrophoretic mobility of mutant and wild type nucleic acid is compared (Orita et al., PNAS 86:2766 (1989); Cotton et al., Mutat. Res. 285:125-144 (1993); and Hayashi et al., Genet. Anal. Tech. Appl 9:73-79 (1992)), and movement of mutant or wild-type fragments in polyacrylamide gels containing a gradient of denaturant is assayed using denaturing gradient gel electrophoresis (Myers et al., Nature 313:495 (1985)). Examples of other techniques for detecting point mutations include selective oligonucleotide hybridization, selective amplification, and selective primer extension.

The nucleic acid molecules are also useful for testing an individual for a genotype that while not necessarily causing the disease, nevertheless affects the treatment modality. Thus, the nucleic acid molecules can be used to study the relationship between an individual's genotype and the individual's response to a compound used for treatment (pharmacogenomic relationship). Accordingly, the nucleic acid molecules described herein can be used to assess the mutation content of the transporter gene in an individual in order to select an appropriate compound or dosage regimen for treatment. FIG. 3 provides information on SNPs that have been found in the gene encoding the transporter protein of the present invention. SNPs, including insertion/deletion polymorphisms (“indels”), were identifed at 87 different nucleotide positions. Changes in the amino acid sequence caused by these SNPs can readily be determined using the universal genetic code and the protein sequence provided in FIG. 2 as a reference. SNPs outside the ORF and in introns may affect control/regulatory elements. SNP positioning in exons, introns, or outside the ORF can readily be determined based on the genomic features given in FIG. 3 .

Thus nucleic acid molecules displaying genetic variations that affect treatment provide a diagnostic target that can be used to tailor treatment in an individual. Accordingly, the production of recombinant cells and animals containing these polymorphisms allow effective clinical design of treatment compounds and dosage regimens.

The nucleic acid molecules are thus useful as antisense constructs to control transporter gene expression in cells, tissues, and organisms. A DNA antisense nucleic acid molecule is designed to be complementary to a region of the gene involved in transcription, preventing transcription and hence production of transporter protein. An antisense RNA or DNA nucleic acid molecule would hybridize to the mRNA and thus block translation of mRNA into transporter protein.

Alternatively, a class of antisense molecules can be used to inactivate mRNA in order to decrease expression of transporter nucleic acid. Accordingly, these molecules can treat a disorder characterized by abnormal or undesired transporter nucleic acid expression. This technique involves cleavage by means of ribozymes containing nucleotide sequences complementary to one or more regions in the mRNA that attenuate the ability of the mRNA to be translated. Possible regions include coding regions and particularly coding regions corresponding to the catalytic and other functional activities of the transporter protein, such as ligand binding.

The nucleic acid molecules also provide vectors for gene therapy in patients containing cells that are aberrant in transporter gene expression. Thus, recombinant cells, which include the patient's cells that have been engineered ex vivo and returned to the patient, are introduced into an individual where the cells produce the desired transporter protein to treat the individual.

The invention also encompasses kits for detecting the presence of a transporter nucleic acid in a biological sample. Experimental data as provided in FIG. 1 indicates that the transporter protein of the present invention is expressed in humans in the testis, brain (adult and fetal), placenta, and bone marrow, as indicated by PCR-based tissue screening panels. For example, the kit can comprise reagents such as a labeled or labelable nucleic acid or agent capable of detecting transporter nucleic acid in a biological sample; means for determining the amount of transporter nucleic acid in the sample; and means for comparing the amount of transporter nucleic acid in the sample with a standard. The compound or agent can be packaged in a suitable container. The kit can further comprise instructions for using the kit to detect transporter protein MRNA or DNA.

Nucleic Acid Arrays

The present invention further provides nucleic acid detection kits, such as arrays or microarrays of nucleic acid molecules that are based on the sequence information provided in FIGS. 1 and 3 (SEQ ID NOS:1 and 3).

As used herein “Arrays” or “Microarrays” refers to an array of distinct polynucleotides or oligonucleotides synthesized on a substrate, such as paper, nylon or other type of membrane, filter, chip, glass slide, or any other suitable solid support. In one embodiment, the microarray is prepared and used according to the methods described in U.S. Pat. No. 5,837,832, Chee et al., PCT application WO95/11995 (Chee et al.), Lockhart, D. J. et al. (1996; Nat. Biotech. 14: 1675-1680) and Schena, M. et aL. (1996; Proc. Natl. Acad. Sci. 93: 10614-10619), all of which are incorporated herein in their entirety by reference. In other embodiments, such arrays are produced by the methods described by Brown et al., U.S. Pat. No. 5,807,522.

The microarray or detection kit is preferably composed of a large number of unique, single-stranded nucleic acid sequences, usually either synthetic antisense oligonucleotides or fragments of cDNAs, fixed to a solid support. The oligonucleotides are preferably about 6-60 nucleotides in length, more preferably 15-30 nucleotides in length, and most preferably about 20-25 nucleotides in length. For a certain type of microarray or detection kit, it may be preferable to use oligonucleotides that are only 7-20 nucleotides in length. The microarray or detection kit may contain oligonucleotides that cover the known 5′, or 3′, sequence, sequential oligonucleotides that cover the full length sequence; or unique oligonucleotides selected from particular areas along the length of the sequence. Polynucleotides used in the microarray or detection kit may be oligonucleotides that are specific to a gene or genes of interest.

In order to produce oligonucleotides to a known sequence for a microarray or detection kit, the gene(s) of interest (or an ORF identified from the contigs of the present invention) is typically examined using a computer algorithm which starts at the 5′ or at the 3′ end of the nucleotide sequence. Typical algorithms will then identify oligomers of defined length that are unique to the gene, have a GC content within a range suitable for hybridization, and lack predicted secondary structure that may interfere with hybridization. In certain situations it may be appropriate to use pairs of oligonucleotides on a microarray or detection kit. The “pairs” will be identical, except for one nucleotide that preferably is located in the center of the sequence. The second oligonucleotide in the pair (mismatched by one) serves as a control. The number of oligonucleotide pairs may range from two to one million. The oligomers are synthesized at designated areas on a substrate using a light-directed chemical process. The substrate may be paper, nylon or other type of membrane, filter, chip, glass slide or any other suitable solid support.

In another aspect, an oligonucleotide may be synthesized on the surface of the substrate by using a chemical coupling procedure and an ink jet application apparatus, as described in PCT application WO95/251116 (Baldeschweiler et al.) which is incorporated herein in its entirety by reference. In another aspect, a “gridded” array analogous to a dot (or slot) blot may be used to arrange and link cDNA fragments or oligonucleotides to the surface of a substrate using a vacuum system, thermal, UV, mechanical or chemical bonding procedures. An array, such as those described above, may be produced by hand or by using available devices (slot blot or dot blot apparatus), materials (any suitable solid support), and machines (including robotic instruments), and may contain 8, 24, 96, 384, 1536, 6144 or more oligonucleotides, or any other number between two and one million which lends itself to the efficient use of commercially available instrumentation.

In order to conduct sample analysis using a microarray or detection kit, the RNA or DNA from a biological sample is made into hybridization probes. The mRNA is isolated, and cDNA is produced and used as a template to make antisense RNA (aRNA). The aRNA is amplified in the presence of fluorescent nucleotides, and labeled probes are incubated with the microarray or detection kit so that the probe sequences hybridize to complementary oligonucleotides of the microarray or detection kit. Incubation conditions are adjusted so that hybridization occurs with precise complementary matches or with various degrees of less complementarity. After removal of nonhybridized probes, a scanner is used to determine the levels and patterns of fluorescence. The scanned images are examined to determine degree of complementarity and the relative abundance of each oligonucleotide sequence on the microarray or detection kit. The biological samples may be obtained from any bodily fluids (such as blood, urine, saliva, phlegm, gastric juices, etc.), cultured cells, biopsies, or other tissue preparations. A detection system may be used to measure the absence, presence, and amount of hybridization for all of the distinct sequences simultaneously. This data may be used for large-scale correlation studies on the sequences, expression patterns, mutations, variants, or polymorphisms among samples.

Using such arrays, the present invention provides methods to identify the expression of the transporter proteins/peptides of the present invention. In detail, such methods comprise incubating a test sample with one or more nucleic acid molecules and assaying for binding of the nucleic acid molecule with components within the test sample. Such assays will typically involve arrays comprising many genes, at least one of which is a gene of the present invention and or alleles of the transporter gene of the present invention. FIG. 3 provides information on SNPs that have been found in the gene encoding the transporter protein of the present invention. SNPs, including insertion/deletion polymorphisms (“indels”), were identifed at 87 different nucleotide positions. Changes in the amino acid sequence caused by these SNPs can readily be determined using the universal genetic code and the protein sequence provided in FIG. 2 as a reference. SNPs outside the ORF and in introns may affect control/regulatory elements. SNP positioning in exons, introns, or outside the ORF can readily be determined based on the genomic features given in FIG. 3 .

Conditions for incubating a nucleic acid molecule with a test sample vary. Incubation conditions depend on the format employed in the assay, the detection methods employed, and the type and nature of the nucleic acid molecule used in the assay. One skilled in the art will recognize that any one of the commonly available hybridization, amplification or array assay formats can readily be adapted to employ the novel fragments of the Human genome disclosed herein. Examples of such assays can be found in Chard, T, An Introduction to Radioimmunoassay and Related Techniques, Elsevier Science Publishers, Amsterdam, The Netherlands (1986); Bullock, G. R. et al., Techniques in Immunocytochemistry, Academic Press, Orlando, Fla. Vol. 1 (1982), Vol. 2 (1983), Vol. 3 (1985); Tijssen, P., Practice and Theory of Enzyme Immunoassays: Laboratory Techniques in Biochemistry and Molecular Biology, Elsevier Science Publishers, Amsterdam, The Netherlands (1985).

The test samples of the present invention include cells, protein or membrane extracts of cells. The test sample used in the above-described method will vary based on the assay format, nature of the detection method and the tissues, cells or extracts used as the sample to be assayed. Methods for preparing nucleic acid extracts or of cells are well known in the art and can be readily be adapted in order to obtain a sample that is compatible with the system utilized.

In another embodiment of the present invention, kits are provided which contain the necessary reagents to carry out the assays of the present invention.

Specifically, the invention provides a compartmentalized kit to receive, in close confinement, one or more containers which comprises: (a) a first container comprising one of the nucleic acid molecules that can bind to a fragment of the Human genome disclosed herein; and (b) one or more other containers comprising one or more of the following: wash reagents, reagents capable of detecting presence of a bound nucleic acid.

In detail, a compartmentalized kit includes any kit in which reagents are contained in separate containers. Such containers include small glass containers, plastic containers, strips of plastic, glass or paper, or arraying material such as silica. Such containers allows one to efficiently transfer reagents from one compartment to another compartment such that the samples and reagents are not cross-contaminated, and the agents or solutions of each container can be added in a quantitative fashion from one compartment to another. Such containers will include a container which will accept the test sample, a container which contains the nucleic acid probe, containers which contain wash reagents (such as phosphate buffered saline, Tris-buffers, etc.), and containers which contain the reagents used to detect the bound probe. One skilled in the art will readily recognize that the previously unidentified transporter gene of the present invention can be routinely identified using the sequence information disclosed herein can be readily incorporated into one of the established kit formats which are well known in the art, particularly expression arrays.

Vectors/Host Cells

The invention also provides vectors containing the nucleic acid molecules described herein. The term “vector” refers to a vehicle, preferably a nucleic acid molecule, which can transport the nucleic acid molecules. When the vector is a nucleic acid molecule, the nucleic acid molecules are covalently linked to the vector nucleic acid. With this aspect of the invention, the vector includes a plasmid, single or double stranded phage, a single or double stranded RNA or DNA viral vector, or artificial chromosome, such as a BAC, PAC, YAC, OR MAC.

A vector can be maintained in the host cell as an extrachromosomal element where it replicates and produces additional copies of the nucleic acid molecules. Alternatively, the vector may integrate into the host cell genome and produce additional copies of the nucleic acid molecules when the host cell replicates.

The invention provides vectors for the maintenance (cloning vectors) or vectors for expression (expression vectors) of the nucleic acid molecules. The vectors can function in procaryotic or eukaryotic cells or in both (shuttle vectors).

Expression vectors contain cis-acting regulatory regions that are operably linked in the vector to the nucleic acid molecules such that transcription of the nucleic acid molecules is allowed in a host cell. The nucleic acid molecules can be introduced into the host cell with a separate nucleic acid molecule capable of affecting transcription. Thus, the second nucleic acid molecule may provide a trans-acting factor interacting with the cis-regulatory control region to allow transcription of the nucleic acid molecules from the vector. Alternatively, a trans-acting factor may be supplied by the host cell. Finally, a trans-acting factor can be produced from the vector itself. It is understood, however, that in some embodiments, transcription and/or translation of the nucleic acid molecules can occur in a cell-free system.

The regulatory sequence to which the nucleic acid molecules described herein can be operably linked include promoters for directing mRNA transcription. These include, but are not limited to, the left promoter from bacteriophage λ, the lac, TRP, and TAC promoters from E. coli, the early and late promoters from SV40, the CMV immediate early promoter, the adenovirus early and late promoters, and retrovirus long-terminal repeats.

In addition to control regions that promote transcription, expression vectors may also include regions that modulate transcription, such as repressor binding sites and enhancers. Examples include the SV40 enhancer, the cytomegalovirus immediate early enhancer, polyoma enhancer, adenovirus enhancers, and retrovirus LTR enhancers.

In addition to containing sites for transcription initiation and control, expression vectors can also contain sequences necessary for transcription termination and, in the transcribed region a ribosome binding site for translation. Other regulatory control elements for expression include initiation and termination codons as well as polyadenylation signals. The person of ordinary skill in the art would be aware of the numerous regulatory sequences that are useful in expression vectors. Such regulatory sequences are described, for example, in Sambrook et al., Molecular Cloning: A Laboratory Manual. 2nd. ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., (1989).

A variety of expression vectors can be used to express a nucleic acid molecule. Such vectors include chromosomal, episomal, and virus-derived vectors, for example vectors derived from bacterial plasmids, from bacteriophage, from yeast episomes, from yeast chromosomal elements, including yeast artificial chromosomes, from viruses such as baculoviruses, papovaviruses such as SV40, Vaccinia viruses, adenoviruses, poxviruses, pseudorabies viruses, and retroviruses. Vectors may also be derived from combinations of these sources such as those derived from plasmid and bacteriophage genetic elements, e.g. cosmids and phagemids. Appropriate cloning and expression vectors for prokaryotic and eukaryotic hosts are described in Sambrook et al, Molecular Cloning: A Laboratory Manual. 2nd. ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., (1989).

The regulatory sequence may provide constitutive expression in one or more host cells (i.e. tissue specific) or may provide for inducible expression in one or more cell types such as by temperature, nutrient additive, or exogenous factor such as a hormone or other ligand. A variety of vectors providing for constitutive and inducible expression in prokaryotic and eukaryotic hosts are well known to those of ordinary skill in the art.

The nucleic acid molecules can be inserted into the vector nucleic acid by well-known methodology. Generally, the DNA sequence that will ultimately be expressed is joined to an expression vector by cleaving the DNA sequence and the expression vector with one or more restriction enzymes and then ligating the fragments together. Procedures for restriction enzyme digestion and ligation are well known to those of ordinary skill in the art.

The vector containing the appropriate nucleic acid molecule can be introduced into an appropriate host cell for propagation or expression using well-known techniques. Bacterial cells include, but are not limited to, E. coli, Streptomyces, and Salmonella typhimurium. Eukaryotic cells include, but are not limited to, yeast, insect cells such as Drosophila, animal cells such as COS and CHO cells, and plant cells.

As described herein, it may be desirable to express the peptide as a fusion protein. Accordingly, the invention provides fusion vectors that allow for the production of the peptides. Fusion vectors can increase the expression of a recombinant protein, increase the solubility of the recombinant protein, and aid in the purification of the protein by acting for example as a ligand for affinity purification. A proteolytic cleavage site may be introduced at the junction of the fusion moiety so that the desired peptide can ultimately be separated from the fusion moiety. Proteolytic enzymes include, but are not limited to, factor Xa, thrombin, and enterotransporter. Typical fusion expression vectors include pGEX (Smith et al., Gene 67:31-40 (1988)), pMAL (New England Biolabs, Beverly, Mass.) and pRIT5 (Pharmacia, Piscataway, N.J.) which fuse glutathione S-transferase (GST), maltose E binding protein, or protein A, respectively, to the target recombinant protein. Examples of suitable inducible non-fusion E. coli expression vectors include pTrc (Amann et al., Gene 69:301-315 (1988)) and pET 11 d (Studier et al., Gene Expression Technology: Methods in Enzymology 185:60-89 (1990)).

Recombinant protein expression can be maximized in host bacteria by providing a genetic background wherein the host cell has an impaired capacity to proteolytically cleave the recombinant protein. (Gottesman, S., Gene Expression Technology: Methods in Enzymology 185, Academic Press, San Diego, Calif. (1990)119-128). Alternatively, the sequence of the nucleic acid molecule of interest can be altered to provide preferential codon usage for a specific host cell, for example E. coli. (Wada et al, Nucleic Acids Res. 20:2111-2118 (1992)).

The nucleic acid molecules can also be expressed by expression vectors that are operative in yeast. Examples of vectors for expression in yeast e.g., S. cerevisiae include pYepSec1 (Baldari, et al., EMBO J. 6:229-234 (1987)), pMFa (Kujan et al., Cell 30:933-943(1982)), pJRY88 (Schultz et al., Gene 54:113-123 (1987)), and pYES2 (Invitrogen Corporation, San Diego, Calif.).

The nucleic acid molecules can also be expressed in insect cells using, for example, baculovirus expression vectors. Baculovirus vectors available for expression of proteins in cultured insect cells (e.g., Sf9 cells) include the pAc series (Smith et al., Mol. Cell Biol. 3:2156-2165 (1983)) and the pVL series (Lucklow et al., Virology 170:31-39 (1989)).

In certain embodiments of the invention, the nucleic acid molecules described herein are expressed in mammalian cells using mammalian expression vectors. Examples of mammalian expression vectors include pCDM8 (Seed, B. Nature 329:840 (1987)) and pMT2PC (Kaufman et al, EMBO J. 6:187-195 (1987)).

The expression vectors listed herein are provided by way of example only of the well-known vectors available to those of ordinary skill in the art that would be useful to express the nucleic acid molecules. The person of ordinary skill in the art would be aware of other vectors suitable for maintenance propagation or expression of the nucleic acid molecules described herein. These are found for example in Sambrook, J., Fritsh, E. F., and Maniatis, T. Molecular Cloning: A Laboratory Manual. 2nd, ed., Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989.

The invention also encompasses vectors in which the nucleic acid sequences described herein are cloned into the vector in reverse orientation, but operably linked to a regulatory sequence that permits transcription of antisense RNA. Thus, an antisense transcript can be produced to all, or to a portion, of the nucleic acid molecule sequences described herein, including both coding and non-coding regions. Expression of this antisense RNA is subject to each of the parameters described above in relation to expression of the sense RNA (regulatory sequences, constitutive or inducible expression, tissue-specific expression).

The invention also relates to recombinant host cells containing the vectors described herein. Host cells therefore include prokaryotic cells, lower eukaryotic cells such as yeast, other eukaryotic cells such as insect cells, and higher eukaryotic cells such as mammalian cells.

The recombinant host cells are prepared by introducing the vector constructs described herein into the cells by techniques readily available to the person of ordinary skill in the art. These include, but are not limited to, calcium phosphate transfection, DEAE-dextran-mediated transfection, cationic lipid-mediated transfection, electroporation, transduction, infection, lipofection, and other techniques such as those found in Sambrook, et al. ( Molecular Cloning: A Laboratory Manual. 2 nd , ed., Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989).

Host cells can contain more than one vector. Thus, different nucleotide sequences can be introduced on different vectors of the same cell. Similarly, the nucleic acid molecules can be introduced either alone or with other nucleic acid molecules that are not related to the nucleic acid molecules such as those providing trans-acting factors for expression vectors. When more than one vector is introduced into a cell, the vectors can be introduced independently, co-introduced or joined to the nucleic acid molecule vector.

In the case of bacteriophage and viral vectors, these can be introduced into cells as packaged or encapsulated virus by standard procedures for infection and transduction. Viral vectors can be replication-competent or replication-defective. In the case in which viral replication is defective, replication will occur in host cells providing functions that complement the defects.

Vectors generally include selectable markers that enable the selection of the subpopulation of cells that contain the recombinant vector constructs. The marker can be contained in the same vector that contains the nucleic acid molecules described herein or may be on a separate vector. Markers include tetracycline or ampicillin-resistance genes for prokaryotic host cells and dihydrofolate reductase or neomycin resistance for eukaryotic host cells. However, any marker that provides selection for a phenotypic trait will be effective.

While the mature proteins can be produced in bacteria, yeast, mammalian cells, and other cells under the control of the appropriate regulatory sequences, cell-free transcription and translation systems can also be used to produce these proteins using RNA derived from the DNA constructs described herein.

Where secretion of the peptide is desired, which is difficult to achieve with multi-transmembrane domain containing proteins such as transporters, appropriate secretion signals are incorporated into the vector. The signal sequence can be endogenous to the peptides or heterologous to these peptides.

Where the peptide is not secreted into the medium, which is typically the case with transporters, the protein can be isolated from the host cell by standard disruption procedures, including freeze thaw, sonication, mechanical disruption, use of lysing agents and the like. The peptide can then be recovered and purified by well-known purification methods including ammonium sulfate precipitation, acid extraction, anion or cationic exchange chromatography, phosphocellulose chromatography, hydrophobic-interaction chromatography, affinity chromatography, hydroxylapatite chromatography, lectin chromatography, or high performance liquid chromatography.

It is also understood that depending upon the host cell in recombinant production of the peptides described herein, the peptides can have various glycosylation patterns, depending upon the cell, or maybe non-glycosylated as when produced in bacteria. In addition, the peptides may include an initial modified methionine in some cases as a result of a host-mediated process.

Uses of Vectors and Host Cells

The recombinant host cells expressing the peptides described herein have a variety of uses. First, the cells are useful for producing a transporter protein or peptide that can be further purified to produce desired amounts of transporter protein or fragments. Thus, host cells containing expression vectors are useful for peptide production.

Host cells are also useful for conducting cell-based assays involving the transporter protein or transporter protein fragments, such as those described above as well as other formats known in the art. Thus, a recombinant host cell expressing a native transporter protein is useful for assaying compounds that stimulate or inhibit transporter protein function.

Host cells are also useful for identifying transporter protein mutants in which these functions are affected. If the mutants naturally occur and give rise to a pathology, host cells containing the mutations are useful to assay compounds that have a desired effect on the mutant transporter protein (for example, stimulating or inhibiting function) which may not be indicated by their effect on the native transporter protein.

Genetically engineered host cells can be further used to produce non-human transgenic animals. A transgenic animal is preferably a mammal, for example a rodent, such as a rat or mouse, in which one or more of the cells of the animal include a transgene. A transgene is exogenous DNA that is integrated into the genome of a cell from which a transgenic animal develops and which remains in the genome of the mature animal in one or more cell types or tissues of the transgenic animal. These animals are useful for studying the function of a transporter protein and identifying and evaluating modulators of transporter protein activity. Other examples of transgenic animals include non-human primates, sheep, dogs, cows, goats, chickens, and amphibians.

A transgenic animal can be produced by introducing nucleic acid into the male pronuclei of a fertilized oocyte, e.g., by microinjection, retroviral infection, and allowing the oocyte to develop in a pseudopregnant female foster animal. Any of the transporter protein nucleotide sequences can be introduced as a transgene into the genome of a non-human animal, such as a mouse.

Any of the regulatory or other sequences useful in expression vectors can form part of the transgenic sequence. This includes intronic sequences and polyadenylation signals, if not already included. A tissue-specific regulatory sequence(s) can be operably linked to the transgene to direct expression of the transporter protein to particular cells.

Methods for generating transgenic animals via embryo manipulation and microinjection, particularly animals such as mice, have become conventional in the art and are described, for example, in U.S. Pat. Nos. 4,736,866 and 4,870,009, both by Leder et al., U.S. Pat. No. 4,873,191 by Wagner et al. and in Hogan, B., Manipulating the Mouse Embryo, (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1986). Similar methods are used for production of other transgenic animals. A transgenic founder animal can be identified based upon the presence of the transgene in its genome and/or expression of transgenic mRNA in tissues or cells of the animals. A transgenic founder animal can then be used to breed additional animals carrying the transgene. Moreover, transgenic animals carrying a transgene can further be bred to other transgenic animals carrying other transgenes. A transgenic animal also includes animals in which the entire animal or tissues in the animal have been produced using the homologously recombinant host cells described herein.

In another embodiment, transgenic non-human animals can be produced which contain selected systems that allow for regulated expression of the transgene. One example of such a system is the cre/loxP recombinase system of bacteriophage P1. For a description of the cre/loxP recombinase system, see, e.g., Lakso et al. PNAS 89:6232-6236 (1992). Another example of a recombinase system is the FLP recombinase system of S. cerevisiae (O'Gorman et al. Science 251:1351-1355 (1991). If a cre/loxP recombinase system is used to regulate expression of the transgene, animals containing transgenes encoding both the Cre recombinase and a selected protein is required. Such animals can be provided through the construction of “double” transgenic animals, e.g., by mating two transgenic animals, one containing a transgene encoding a selected protein and the other containing a transgene encoding a recombinase.

Clones of the non-human transgenic animals described herein can also be produced according to the methods described in Wilmut, I. et al. Nature 385:810-813 (1997) and PCT International Publication Nos. WO 97/07668 and WO 97/07669. In brief, a cell, e.g., a somatic cell, from the transgenic animal can be isolated and induced to exit the growth cycle and enter G o phase. The quiescent cell can then be fused, e.g., through the use of electrical pulses, to an enucleated oocyte from an animal of the same species from which the quiescent cell is isolated. The reconstructed oocyte is then cultured such that it develops to morula or blastocyst and then transferred to pseudopregnant female foster animal. The offspring born of this female foster animal will be a clone of the animal from which the cell, e.g., the somatic cell, is isolated.

Transgenic animals containing recombinant cells that express the peptides described herein are useful to conduct the assays described herein in an in vivo context. Accordingly, the various physiological factors that are present in vivo and that could effect ligand binding, transporter protein activation, and signal transduction, may not be evident from in vitro cell-free or cell-based assays. Accordingly, it is useful to provide non-human transgenic animals to assay in vivo transporter protein function, including ligand interaction, the effect of specific mutant transporter proteins on transporter protein function and ligand interaction, and the effect of chimeric transporter proteins. It is also possible to assess the effect of null mutations, that is mutations that substantially or completely eliminate one or more transporter protein functions.

All publications and patents mentioned in the above specification are herein incorporated by reference. Various modifications and variations of the described method and system of the invention will be apparent to those skilled in the art without departing from the scope and spirit of the invention. Although the invention has been described in connection with specific preferred embodiments, it should be understood that the invention as claimed should not be unduly limited to such specific embodiments. Indeed, various modifications of the above-described modes for carrying out the invention which are obvious to those skilled in the field of molecular biology or related fields are intended to be within the scope of the following claims.

<160> NUMBER OF SEQ ID NOS: 4

<210> SEQ ID NO 1

<211> LENGTH: 5735

<212> TYPE: DNA

<213> ORGANISM: Human

<400> SEQUENCE: 1

cggccgcgtc gacgtgattt gatatcttga tgatggctta aacagatact ga

#tggacaga     60

tctgttgttt gatatttttt tcactagccc tgaagatgct gagacataga ga

#tggctgtg    120

attatctttt gtaagacagg aaatgcagtc tttaggggtt tctggaaata ga

#aaggtcat    180

gcagtctgga acctgtgagc cttttcaatc tctaagtcat cagagaaatg at

#gaagaagc    240

agttgtggat agaggtggaa ctcgttctat tctcaaaaca cactttgaga aa

#gaagattt    300

agaaggtcat cgaacactat ttattggagt acatgtgccc ttgggaggaa ga

#aaaagcca    360

tcgacgtcac aggcatcgtg gtcataaaca cagaaagaga gacagagaaa ga

#gattcagg    420

attagaggat ggaagggagt caccttcttt tgacacccca tcacagaggg ta

#cagtttat    480

tcttggaacc gaggatgatg acgaggaaca cattcctcat gaccttttca ca

#gaactgga    540

tgagatttgt tggcgtgaag gtgaggacgc tgagtggcga gaaacagcca gg

#tggttgaa    600

gtttgaagaa gatgtggaag atggaggaga aaggtggagc aagccttatg tg

#gctactct    660

ttcattgcac agcttgtttg aattgagaag ttgtattctg aatggaactg tg

#ttgctgga    720

catgcatgcc aacactttag aagaaattgc agatatggtt cttgaccaac aa

#gtgagctc    780

aggtcagctg aatgaagatg tacgccatag ggtccatgag gcattgatga aa

#cagcatca    840

tcatcagaat cagaaaaaac tcaccaacag gattcccatt gttcgttcct tt

#gctgatat    900

tggcaagaaa cagtcagaac caaattccat ggacaaaaat gcaggtcagg tt

#gtttctcc    960

tcagtctgct ccagcctgtg ttgaaaataa aaatgatgtt agcagagaaa ac

#agcactgt   1020

tgactttagc aagggactgg gaggccaaca aaaggggcat actagtccat gt

#gggatgaa   1080

acaaaggcat gaaaaaggac ctccacacca gcaagagaga gaggttgatc tg

#cattttat   1140

gaaaaagatt cctccaggtg ctgaagcatc gaacatctta gtgggagaac tg

#gagttctt   1200

ggatcgaaca gtagttgcgt ttgtcaggtt gtctccagct gtattgcttc aa

#ggactggc   1260

tgaagtccca atcccaacca gatttttgtt cattcttctg ggacccctgg ga

#aagggtca   1320

acagtaccat gagattggca gatcaattgc aaccctaatg acagatgagg ta

#tttcatga   1380

tgttgcctat aaagctaaag atcgtaatga cttggtatca ggaattgatg ag

#tttctgga   1440

tcaggttact gttctccctc ctggagaatg ggatccaagc attcgaatag ag

#cctcccaa   1500

aaatgttcct tcccaggaga agaggaagat tcctgctgta ccaaatggaa ca

#gcagctca   1560

tggggaagca gagccccacg gaggacatag tggacctgaa ctccagcgaa ct

#ggaaggat   1620

ttttggggga cttattttag atatcaaaag aaaagctcca tacttctgga gt

#gacttcag   1680

agatgctttc agcctgcagt gcttagcatc ttttctattt ctctactgcg cg

#tgtatgtc   1740

tcctgtcatc acgtttggag gactgctggg agaagcaact gaagggcgta ta

#agtgcaat   1800

tgaatctctc tttggagcat ccatgaccgg gatagcctat tctctctttg gt

#ggacagcc   1860

tcttaccata ttaggcagta caggaccagt tttggtgttt gaaaagattt tg

#tttaaatt   1920

ttgcaaagaa tatgggctgt catacctatc tttaagagct agcattggac tt

#tggactgc   1980

aactctatgt atcatacttg tggccacaga tgctagttcc cttgtctgct ac

#atcactcg   2040

gtttactgaa gaagcttttg cttccctgat ttgcatcatt ttcatttatg ag

#gccctgga   2100

gaagttgttt gaactcagtg aagcatatcc aatcaacatg cataatgatc tg

#gaactgct   2160

gacacaatac tcgtgtaact gtgtggaacc gcataatccc agcaatggca ca

#ttgaagga   2220

atggagggaa tccaatattt ctgcctctga cataatttgg gagaacctaa ct

#gtgtcaga   2280

atgcaaatca ttgcatggag agtatgttgg acgggcctgt ggccatgatc ac

#ccatatgt   2340

tccagatgtt ctattttggt ctgtgatcct gttcttttcc acagttactc tg

#tcagccac   2400

cctgaagcag ttcaagacta gcagatattt tccaaccaag gttcgatcca ta

#gtgagtga   2460

ctttgctgtc tttcttacaa ttctgtgtat ggttttaatt gactatgcca tt

#gggatccc   2520

atctccaaaa ctacaagtac caagtgtttt caagcccact agagatgatc gt

#ggctggtt   2580

tgttacgcct ttaggtccaa acccatggtg gacagtaata gctgctataa tt

#ccagctct   2640

gctttgtact attctaattt ttatggacca acagattaca gctgtcatca tc

#aacaggaa   2700

agagcataag ctaaagaaag gttgtgggta ccatctggac ctattaatgg tg

#gctgtcat   2760

gctcggtgta tgctccatca tgggcctgcc atggtttgtg gctgccacag tc

#ctctccat   2820

cactcatgtc aatagcctaa aactggaatc agaatgctca gctccaggag aa

#caacccaa   2880

atttctcggc attcgggagc aaagggttac tgggcttatg atttttattc tt

#atgggttc   2940

atcagtcttt atgaccagta ttctgaagtt tattcccatg ccagtgctat at

#ggagtgtt   3000

tctttatatg ggtgcttcat ctctaaaggg aattcagttc tttgatagga ta

#aagctctt   3060

ctggatgccg gcaaaacatc aaccagattt tatataccta aggcacgtac cg

#cttcgaaa   3120

agtgcatctc ttcacaatta ttcagatgag ttgccttggc cttttgtgga ta

#ataaaagt   3180

ttcaagagct gctattgtct ttcccatgat ggtgttagcc ctggtatttg ta

#agaaagtt   3240

gatggacttg ttgttcacga agcgggaact cagctggttg gatgatttga tg

#cccgagag   3300

taagaaaaag aaactggaag atgctgaaaa agaagaagaa caaagtatgc ta

#gctatgga   3360

agatgagggc acagtacaac tcccattgga agggcactat agagatgatc ca

#tctgtgat   3420

caatatatct gatgaaatgt caaagactgc cttgtggagg aaccttctga tt

#actgccga   3480

taactcaaaa gataaggagt caagctttcc ttccaaaagc tccccttcct aa

#tcactcta   3540

gaagctgatt ccccaaagca ttgaaagccg aaaagagaag aaagctgact ca

#gggaaagg   3600

tgttgacagg gagacttgtc tatgactcga tcttcaattt attttttaca ta

#tatatgag   3660

aagagtgtca caattattaa taaaactgct ttgatcatgt attgtaaatt ct

#gtccctca   3720

acccaaatcc accttcatac tgtaagtagt gcaatacttg tttcatttct gt

#gtttaaac   3780

ttctgagcag tgagacatcc ctgtgagcag atacaatagc caatgcaaga at

#ctgtgtgt   3840

tccttgctgt acgttagaca tttgtaaact ggattctgat tgtcagtttt at

#gagagcaa   3900

tagcttcctt aaagagataa gtcatattta cctagtttgt attttcctac tt

#tagtgacc   3960

tgaagatgcc tgataatttc attcagaaga atttttgaaa ggtagtctta ct

#tcttttta   4020

gtttttatag cttagcatta gtgacttatt tcaaaagacc caaatcaaaa ag

#ttagtttg   4080

aaagcatttt ttaataattg tatttatgca tttccttgat ttaatatgat aa

#atttaata   4140

cttaacaatt tatatgtaac taaaacttaa agtcatttga aaaatatata ga

#aacctatt   4200

tacaacttgt taaggacaat cagacataat gcagagttaa gtagtatttg ct

#taaaattc   4260

aagttgtgac taatgatcaa atactaggct tgtacgaaat gctttagaaa aa

#ctttgtaa   4320

cagttttgtg ggatttttca atataaacct ttatcagaaa tatactaagt tt

#gtctccca   4380

ctgacaacag atgttttcca aataaacata ttctatacat acttgtggaa tg

#ccacatgg   4440

tgaatcattg tatatgaaat tccactcctg tacagttact ctgcagctaa tg

#gtcatgca   4500

ctgcttaatg ctggtcctga atcatgttct catgttagac caacagctct cc

#aattgtca   4560

ttttttttct gcagagtttt tttttttcca cttttaaatt aaatgcatgt tg

#tggaaaaa   4620

cagtctttta aaatgaaatt tcagattcca tttgagaagg ttctgtagat at

#ttcagtcc   4680

atataaaata atacatcttt actaaactta tataagggga gagaaagtta tg

#aagttttg   4740

gacattacta aaagtacagt atttgatttc actttcaatg aatgtgaagt ta

#ataaaact   4800

aaatctcata atgctcttgg ttcctaagaa tgagtagtaa tcatcaactt ta

#taatactc   4860

caatattccg ttttataata attcagagcc ctgtggcttt tacacaccgt ta

#attatgta   4920

ctctgttgga agtgcacatg aaaagtgaag aaaagttcct cttgtgatta aa

#ctaatggg   4980

aggaaataaa tcaacaaagt ctccattaag ttctacattt tgagaccttt ta

#aaaattcc   5040

cctcacaatt ctttaaggag cccccctttt tatggaacat gagcctaaaa at

#tatagaaa   5100

gaagaatttt aagttaataa agtttgtatt tataaatgct gaaaaaatac ag

#aaactttc   5160

tgttccaaat gtgttgcctt tgtgtatttt ataatacaga tactacattg ta

#aacatttc   5220

cattgtttta tgatttagcc agtgattccc caaagcagcc tcttagtgtt tt

#aatatatt   5280

aataactgtt ttgttaaaaa tgatcatagt gaatttaaat cttcacatga tc

#acctattt   5340

gaataagcaa tcatatccaa tgaaattctg tatttctgag tatttttata gt

#cattttgt   5400

tcttgtgtga attttaaagc tatccctatg ttaatcctaa tattttgaaa tc

#atataaaa   5460

tataataaaa atgtagtatt atatatttac ttctaatttc agattcctgg tc

#aaaattac   5520

taaatatctt gaatgtaatt tagtgccaag tttaaataat gtgtaaatgt ga

#ctaggata   5580

ttgtgttttt cacaattaag aaatgttatg tggaaataaa tatttatcct aa

#cttccttg   5640

cacattttaa attgtgatac aaagtgtctt gtcttttttc tttgttttaa tt

#agtaaatc   5700

agtgtaaaac aaaaaaaaaa aaaaaaaaaa aaaaa

#

#     5735

<210> SEQ ID NO 2

<211> LENGTH: 1129

<212> TYPE: PRT

<213> ORGANISM: Human

<400> SEQUENCE: 2

Met Gln Ser Leu Gly Val Ser Gly Asn Arg Ly

#s Val Met Gln Ser Gly

1               5

#                10

#                15

Thr Cys Glu Pro Phe Gln Ser Leu Ser His Gl

#n Arg Asn Asp Glu Glu

20

#            25

#            30

Ala Val Val Asp Arg Gly Gly Thr Arg Ser Il

#e Leu Lys Thr His Phe

35

#        40

#        45

Glu Lys Glu Asp Leu Glu Gly His Arg Thr Le

#u Phe Ile Gly Val His

50

#    55

#    60

Val Pro Leu Gly Gly Arg Lys Ser His Arg Ar

#g His Arg His Arg Gly

65

#70

#75

#80

His Lys His Arg Lys Arg Asp Arg Glu Arg As

#p Ser Gly Leu Glu Asp

85

#                90

#                95

Gly Arg Glu Ser Pro Ser Phe Asp Thr Pro Se

#r Gln Arg Val Gln Phe

100

#           105

#           110

Ile Leu Gly Thr Glu Asp Asp Asp Glu Glu Hi

#s Ile Pro His Asp Leu

115

#       120

#       125

Phe Thr Glu Leu Asp Glu Ile Cys Trp Arg Gl

#u Gly Glu Asp Ala Glu

130

#   135

#   140

Trp Arg Glu Thr Ala Arg Trp Leu Lys Phe Gl

#u Glu Asp Val Glu Asp

145                 1

#50                 1

#55                 1

#60

Gly Gly Glu Arg Trp Ser Lys Pro Tyr Val Al

#a Thr Leu Ser Leu His

165

#               170

#               175

Ser Leu Phe Glu Leu Arg Ser Cys Ile Leu As

#n Gly Thr Val Leu Leu

180

#           185

#           190

Asp Met His Ala Asn Thr Leu Glu Glu Ile Al

#a Asp Met Val Leu Asp

195

#       200

#       205

Gln Gln Val Ser Ser Gly Gln Leu Asn Glu As

#p Val Arg His Arg Val

210

#   215

#   220

His Glu Ala Leu Met Lys Gln His His His Gl

#n Asn Gln Lys Lys Leu

225                 2

#30                 2

#35                 2

#40

Thr Asn Arg Ile Pro Ile Val Arg Ser Phe Al

#a Asp Ile Gly Lys Lys

245

#               250

#               255

Gln Ser Glu Pro Asn Ser Met Asp Lys Asn Al

#a Gly Gln Val Val Ser

260

#           265

#           270

Pro Gln Ser Ala Pro Ala Cys Val Glu Asn Ly

#s Asn Asp Val Ser Arg

275

#       280

#       285

Glu Asn Ser Thr Val Asp Phe Ser Lys Gly Le

#u Gly Gly Gln Gln Lys

290

#   295

#   300

Gly His Thr Ser Pro Cys Gly Met Lys Gln Ar

#g His Glu Lys Gly Pro

305                 3

#10                 3

#15                 3

#20

Pro His Gln Gln Glu Arg Glu Val Asp Leu Hi

#s Phe Met Lys Lys Ile

325

#               330

#               335

Pro Pro Gly Ala Glu Ala Ser Asn Ile Leu Va

#l Gly Glu Leu Glu Phe

340

#           345

#           350

Leu Asp Arg Thr Val Val Ala Phe Val Arg Le

#u Ser Pro Ala Val Leu

355

#       360

#       365

Leu Gln Gly Leu Ala Glu Val Pro Ile Pro Th

#r Arg Phe Leu Phe Ile

370

#   375

#   380

Leu Leu Gly Pro Leu Gly Lys Gly Gln Gln Ty

#r His Glu Ile Gly Arg

385                 3

#90                 3

#95                 4

#00

Ser Ile Ala Thr Leu Met Thr Asp Glu Val Ph

#e His Asp Val Ala Tyr

405

#               410

#               415

Lys Ala Lys Asp Arg Asn Asp Leu Val Ser Gl

#y Ile Asp Glu Phe Leu

420

#           425

#           430

Asp Gln Val Thr Val Leu Pro Pro Gly Glu Tr

#p Asp Pro Ser Ile Arg

435

#       440

#       445

Ile Glu Pro Pro Lys Asn Val Pro Ser Gln Gl

#u Lys Arg Lys Ile Pro

450

#   455

#   460

Ala Val Pro Asn Gly Thr Ala Ala His Gly Gl

#u Ala Glu Pro His Gly

465                 4

#70                 4

#75                 4

#80

Gly His Ser Gly Pro Glu Leu Gln Arg Thr Gl

#y Arg Ile Phe Gly Gly

485

#               490

#               495

Leu Ile Leu Asp Ile Lys Arg Lys Ala Pro Ty

#r Phe Trp Ser Asp Phe

500

#           505

#           510

Arg Asp Ala Phe Ser Leu Gln Cys Leu Ala Se

#r Phe Leu Phe Leu Tyr

515

#       520

#       525

Cys Ala Cys Met Ser Pro Val Ile Thr Phe Gl

#y Gly Leu Leu Gly Glu

530

#   535

#   540

Ala Thr Glu Gly Arg Ile Ser Ala Ile Glu Se

#r Leu Phe Gly Ala Ser

545                 5

#50                 5

#55                 5

#60

Met Thr Gly Ile Ala Tyr Ser Leu Phe Gly Gl

#y Gln Pro Leu Thr Ile

565

#               570

#               575

Leu Gly Ser Thr Gly Pro Val Leu Val Phe Gl

#u Lys Ile Leu Phe Lys

580

#           585

#           590

Phe Cys Lys Glu Tyr Gly Leu Ser Tyr Leu Se

#r Leu Arg Ala Ser Ile

595

#       600

#       605

Gly Leu Trp Thr Ala Thr Leu Cys Ile Ile Le

#u Val Ala Thr Asp Ala

610

#   615

#   620

Ser Ser Leu Val Cys Tyr Ile Thr Arg Phe Th

#r Glu Glu Ala Phe Ala

625                 6

#30                 6

#35                 6

#40

Ser Leu Ile Cys Ile Ile Phe Ile Tyr Glu Al

#a Leu Glu Lys Leu Phe

645

#               650

#               655

Glu Leu Ser Glu Ala Tyr Pro Ile Asn Met Hi

#s Asn Asp Leu Glu Leu

660

#           665

#           670

Leu Thr Gln Tyr Ser Cys Asn Cys Val Glu Pr

#o His Asn Pro Ser Asn

675

#       680

#       685

Gly Thr Leu Lys Glu Trp Arg Glu Ser Asn Il

#e Ser Ala Ser Asp Ile

690

#   695

#   700

Ile Trp Glu Asn Leu Thr Val Ser Glu Cys Ly

#s Ser Leu His Gly Glu

705                 7

#10                 7

#15                 7

#20

Tyr Val Gly Arg Ala Cys Gly His Asp His Pr

#o Tyr Val Pro Asp Val

725

#               730

#               735

Leu Phe Trp Ser Val Ile Leu Phe Phe Ser Th

#r Val Thr Leu Ser Ala

740

#           745

#           750

Thr Leu Lys Gln Phe Lys Thr Ser Arg Tyr Ph

#e Pro Thr Lys Val Arg

755

#       760

#       765

Ser Ile Val Ser Asp Phe Ala Val Phe Leu Th

#r Ile Leu Cys Met Val

770

#   775

#   780

Leu Ile Asp Tyr Ala Ile Gly Ile Pro Ser Pr

#o Lys Leu Gln Val Pro

785                 7

#90                 7

#95                 8

#00

Ser Val Phe Lys Pro Thr Arg Asp Asp Arg Gl

#y Trp Phe Val Thr Pro

805

#               810

#               815

Leu Gly Pro Asn Pro Trp Trp Thr Val Ile Al

#a Ala Ile Ile Pro Ala

820

#           825

#           830

Leu Leu Cys Thr Ile Leu Ile Phe Met Asp Gl

#n Gln Ile Thr Ala Val

835

#       840

#       845

Ile Ile Asn Arg Lys Glu His Lys Leu Lys Ly

#s Gly Cys Gly Tyr His

850

#   855

#   860

Leu Asp Leu Leu Met Val Ala Val Met Leu Gl

#y Val Cys Ser Ile Met

865                 8

#70                 8

#75                 8

#80

Gly Leu Pro Trp Phe Val Ala Ala Thr Val Le

#u Ser Ile Thr His Val

885

#               890

#               895

Asn Ser Leu Lys Leu Glu Ser Glu Cys Ser Al

#a Pro Gly Glu Gln Pro

900

#           905

#           910

Lys Phe Leu Gly Ile Arg Glu Gln Arg Val Th

#r Gly Leu Met Ile Phe

915

#       920

#       925

Ile Leu Met Gly Ser Ser Val Phe Met Thr Se

#r Ile Leu Lys Phe Ile

930

#   935

#   940

Pro Met Pro Val Leu Tyr Gly Val Phe Leu Ty

#r Met Gly Ala Ser Ser

945                 9

#50                 9

#55                 9

#60

Leu Lys Gly Ile Gln Phe Phe Asp Arg Ile Ly

#s Leu Phe Trp Met Pro

965

#               970

#               975

Ala Lys His Gln Pro Asp Phe Ile Tyr Leu Ar

#g His Val Pro Leu Arg

980

#           985

#           990

Lys Val His Leu Phe Thr Ile Ile Gln Met Se

#r Cys Leu Gly Leu Leu

995

#       1000

#      1005

Trp Ile Ile Lys Val Ser Arg Ala Ala Ile Va

#l Phe Pro Met Met Val

1010

#   1015

#  1020

Leu Ala Leu Val Phe Val Arg Lys Leu Met As

#p Leu Leu Phe Thr Lys

1025                1030

#                1035

#               1040

Arg Glu Leu Ser Trp Leu Asp Asp Leu Met Pr

#o Glu Ser Lys Lys Lys

1045

#               1050

#              1055

Lys Leu Glu Asp Ala Glu Lys Glu Glu Glu Gl

#n Ser Met Leu Ala Met

1060

#           1065

#          1070

Glu Asp Glu Gly Thr Val Gln Leu Pro Leu Gl

#u Gly His Tyr Arg Asp

1075

#       1080

#      1085

Asp Pro Ser Val Ile Asn Ile Ser Asp Glu Me

#t Ser Lys Thr Ala Leu

1090

#   1095

#  1100

Trp Arg Asn Leu Leu Ile Thr Ala Asp Asn Se

#r Lys Asp Lys Glu Ser

1105                1110

#                1115

#               1120

Ser Phe Pro Ser Lys Ser Ser Pro Ser

1125

<210> SEQ ID NO 3

<211> LENGTH: 202001

<212> TYPE: DNA

<213> ORGANISM: Human

<220> FEATURE:

<221> NAME/KEY: misc_feature

<222> LOCATION: (1)...(202001)

<223> OTHER INFORMATION: n = A,T,C or G

<400> SEQUENCE: 3

gccttgggag ctgtgagaaa taaatatttg ttgttgtggc attttgttat ag

#cagcccaa     60

atggactaag atacactctt ttggctctct cttcattcag tccaagggtg tt

#ctgctagg    120

ttttggctac tcttcatttc ttttatcaaa tatttgttaa ggcttattag gg

#cctaaagt    180

ctagaggcat tctgctttac tattatgacc atatcttaat aacactggta tg

#agtaacat    240

actgtatgag taaataattt gttttagagc aatggttttc taaaaatggg ag

#atcatagt    300

ttttagtaat taattgtgtt aaattactat taagagggtc aagtaataga tg

#ttaagtaa    360

ttttttggat taaatagatc ttatcaacta gataatagag agattaagag ct

#gctttgca    420

ctcaggtttc atgtttttat tgcaaagatc aattgtgctt acaagaaaac ac

#tgaaggaa    480

attggggatt atatatacta attaataaca tccagagaat gataaaaata tc

#agtgtttg    540

tattcttgct gtgacaaaat acctgaagga aaagttcaat tttcttattt tt

#cattattg    600

attcatttaa taactttgat atgtaatagt ataggagatt aggaatgaac ct

#tgcttgat    660

gtttcgcttt tcctcatttc tcacattcaa tccctgaatt ctatcttttt tc

#aataagat    720

gtgtatctgg atctattcat ttctcttcat tcctattgcc acttctttgg tt

#caggccat    780

catcatcccc tgattgaaat tatttaacat tctcctgatt tgtctcccgt cc

#tccagttt    840

tgttttactc aattgattgt ctatagagta gccgggatat tttaaacctg at

#tatgctga    900

cagtttgtca tttccctaag ggtaaagctc acactcttta aatggctcct ga

#cgcttacc    960

gtgactgggc ctcacttctc atctcttccc tctgttctta cactttatgg tc

#taacctat   1020

gttgtatttg ccattccttg aatgtgacta gatcagaatc ttctgtttta ac

#agtacttc   1080

cctaaggaaa tcttttctga tccctagatt agggtaggat gccttgctac gg

#ctttcatg   1140

tcaactttta attcttcagt tataacaaaa catgcttgtt tgatttatct gc

#tttctgtg   1200

atggcaggtt ttgtgttgtt tgttatggag tccctagcac ctatatagta cc

#tgacacat   1260

agtaagaatt caatattttc tacaggaaag aatgaatata gaaagagaga cg

#atgtagct   1320

taggaaggct ttattgagaa gataggtctt aaaggatgag tacctatttt ga

#ttataata   1380

agagggtaaa tactacatag atggaaatat ttgtttacat gtgatttttc at

#tcagatgt   1440

gttatagtat acatacagca gaataccaag ctctgtgtct ccaacctgtg ca

#gttagagt   1500

cagtagtttt tctaaaagta taatttggat cagcccagtt tcttaagact ca

#ttgtgact   1560

agtctccatc aaatgttgtg agtgaaagaa gggaaactat tcacaggtaa at

#aaagtgtt   1620

catagagtcg tgaattcagg ctattcataa tgtgagggct gtttcaggat aa

#tatgttgc   1680

acttggtgtc ttaattttga atgtagttga attgactata atcttagtct tt

#tttttttt   1740

tggtttgtgt tttctttagt tataaaacac aaccttttgt cacacggtaa ag

#agaaagca   1800

tttccaatta taatttttga gatattgatt ctatattaga acactttatc aa

#tcttaaag   1860

ttccctgatt ctgctatgtt gtggtaaaag aaaacagtac tcaaacttta at

#aaataaga   1920

cacagtgaaa atccatagta aaaatgccaa caacttacat aggtttcatt ac

#tagactta   1980

accgtgcagt tttagcattt gataatacca cattatcttt tgcatgtaaa tt

#ctttagaa   2040

gaagatatta aataaaaaga taaaatgtat gttggtatga agaatctgaa ac

#ataaatga   2100

aatccctgaa aattaaaagg tgaatatgta tttacctatt tactatttac ac

#aactatca   2160

aagattgcca aaataaaaat cctgtatagg cgctcatcat tttgatgggt gg

#ataagtcg   2220

tgatacccat agtttggaag gaagattcct tcaagagagt acaattttgc tt

#ggtaaatc   2280

ttttgcatgt taaacttttt agaagaagaa attaaataaa aatataaaat gt

#atgttggt   2340

atgaagaatc tgaaacataa atgaaattcc tgaaaattaa agggtgaata tg

#tatttacc   2400

tatttactat ttatacaact atcaaagatt gccaaaataa aaatcctttt ta

#ggcactca   2460

tcattttgat gggtggataa gtgatgatat tcagagtttg gagggaaaat tc

#ctttaaga   2520

gagtataatt ttgcttggta agtcataaag cctaaagctt agtcacatat ag

#agaaagct   2580

gcctaataat taagagttga cattttaaca tggtatttgc aacagacaca tt

#ggatactt   2640

aattaaatgg aaaactgctt atttttaaag gactgaaaaa attcaactct cc

#ttggcaaa   2700

tgaagtcttc atagtatcag aaatggggaa atctgaagga tgtggctcat tc

#tctgtttc   2760

gatgatgcag aattgctcta agcagtaagc ttacagtttt cagacagcat ca

#gcaaatac   2820

aactgtgtca gtctctctta gtatggggtg tttgtaactg cacaggggag at

#gataaata   2880

gtatatgtga tttgatatct tgatgatggc ttaaacagat actgatggac ag

#atctgttg   2940

tttgatattt ttttcactag ccctgaagat gctgagacat agagatggct gt

#gattatct   3000

tttgtaagac aggaaatgca gtctttaggg gtttctggaa atagaaaggt ca

#tgcagtct   3060

ggaacctgtg agccttttca atctctaagt catcaggtat gacctcatga at

#tatgatga   3120

taatattaga atgtagggtg cttgcttttt ctagttctta ctcattgaaa at

#atattcat   3180

taatgtaatt gtttattgtc agactttcct taggatattt gaacaagtaa ga

#tttatggc   3240

agctaaacaa tatgattatt agaaatgtgt gtgtatgtgt gtgcctgtgt gt

#gtgtatgt   3300

gtttaaattt gtgtttactt tagctttttg ggggagaggg cggtaaagga ag

#agattctt   3360

tgaatgtgat taaaagcaag gtttggggca cttcagattt ttccagatta ag

#cctgaata   3420

gagtcaatct ttatatttta cttcaagtga taaaaatagt ataaatcgat ca

#aactgata   3480

aggatacatc gtagctagct gcttacagat actgatatat tgcaaatatt tt

#tattattt   3540

ggaatttctt aaccatagaa actgatgctg ctaccattgt agtgtgctac at

#agcaaagg   3600

aagtttggtg aatagaatca tctttgtcag catctgacct ataaactaat tt

#cctgaaat   3660

ttatgttgca ttatctgaac tgttgtaaag acactggttt taatcatttc tc

#agatctat   3720

tgaaatattg atgctcttgg tgcttttaag gtagatatat actaacgtat tg

#ttcataga   3780

agaaaggaga ctataaatct gtttttcaca aagaaagctt gtgacattta ag

#cttgttga   3840

agattttttg acccagagag cttcgtcctt tgcttacttt cattttcaaa ct

#gaaaatac   3900

ttgactatgt taaacatgca aatgatttgg atttcgatgt ccattttgta ct

#gaaactct   3960

gccatttatt ttaaactatt ttcacccatc aagttatata taatgcattt aa

#ctttgatt   4020

tgttacagca tgtcctcaga attatatact tggataagaa actacctata tt

#tgacattc   4080

agattttgaa ggaaatatat ttcatttttc aaaatattgt acatgcttct gc

#ctcaatgt   4140

tagagaactt ttcaggtact ccatattaaa tgatcaaaaa gagagaaata ta

#ttgcagca   4200

gttctcaaca gcaagatggt tttgtcttta tgattctgta gcctgattgt aa

#tttaatgc   4260

cttatcaggg tgaaatgaca tagattaaaa aaatgaatat atttaaggaa gt

#ctgaaaca   4320

atgaattgat tcagttaagg ggtttctcct ttttaattaa aaacacattc tg

#cctactga   4380

tattgactat aatttatatg ttattcaggc tacttagcca gcttatattc tt

#attagtag   4440

ggaagattgg catattctta agcttgatta attttgaaat gatttgaata ta

#ccttttaa   4500

ttgcaacaaa atatgtctaa tctgttagaa tttatttcca gtatttgcat gt

#attagtca   4560

ttatgagtac attctgtttc ttggcattgc tttgggattc ctcttggtat tg

#gtttcaca   4620

gcattctgct atttttcact gtattcctga cctttcaaga gaaccaaact gt

#aaagattt   4680

ttagttactt tctgttagtg gcatttaaat gaggatatcg ataattttgt aa

#ggtggaaa   4740

aaaattacta ttttagaatt gtcatttctg tcacaaatca gagaaatttt tc

#tctattac   4800

tatttcaaaa tatactacaa taaaaagcaa agactggtta gaatgtagtt aa

#atgcaatg   4860

tcaatctttc ttcttgcatg gcaggataat cttgatcttt ggaatgataa aa

#ctgattgt   4920

aaacttgccc agtaatgatt ggtcatcttc cttacaaagg ctgccttcgt tt

#atactatt   4980

ttacatgcat ttcattatac atcataaagg ttttaaaggt aagctgccta ta

#aaaactat   5040

ttgagtaatt cttcaattca gtaaacatag taaaggctga gcattggatg at

#actgtatg   5100

tatttggtgt tatgaggaat gcagaaaaga aaaagtcatt tccggctttc aa

#ggagatta   5160

gtgaatatat gcaatgaatt gtgttcacat tttgaattga tttttgatag gc

#agtatgct   5220

acaatcagtt ttaacttaat ctataagctg atgaatccta gaaggagtta ca

#tgtaacct   5280

tttttcctca tgtaaatttc ttgatattag ataaatgaag gcttaggtca aa

#ctgtatca   5340

ttatgcatcc cataacttta ttgaaaattg cattaaagac ttttagagtg ca

#tagtttct   5400

cgtatagggc tttataaact gtgaatcagt aaaatagcaa aatagctttg ca

#tgttgtat   5460

aagccatcat tgtcagtatg agactgaagg tgcacccagt ccactggcag ga

#ggcagaag   5520

tgtcagctca acatagagac ttgatcaatc ctgtctaatt ccaggctcag tg

#tgggtaat   5580

taagtattat ggaaggggtt ttgactttat agggataaaa cttggaaata aa

#gagtagca   5640

agtatggaag tgtctgttac taactaggtc atttggagag tcctttgaat aa

#aatggggg   5700

aataggattt acctcaggtt ctgagaaagc ggatcaggac caactaatta tg

#gaagtgga   5760

ccttagctgc tgcttggtga acagtcaggc attactctct tctctttcat tc

#caatatgt   5820

ttgctgaaag ttgcaggaag gtgggtggag aagatgcaaa gcccttgttt cc

#ccagaatc   5880

ccaaactgga acacgctgcc tgatagtgcc tccaaagtgc ctgtttcctt gt

#attagagc   5940

aatagaaaat tgatttgcaa attcttctgg tttgtaatgg ctggctgcag ta

#agaggctt   6000

gtgcaatggt tcagtgtctg gactgccatg ttctctgggt tcaaatctta gc

#tatgctac   6060

ttactggctg catgatcttg gcttgtttcc tgatgtgtaa tatagggata at

#aatggcac   6120

ctacctcaaa gagttgtggt aaacattaag tgagttaatg tatgtgaaac ac

#ttataaga   6180

gtacctgaca tatatcaaac atattattgt caacatcctt tgtcgacaga ct

#ttgttata   6240

gacattctaa gaggttggat gggctattgg caagactttg taacagtcat ca

#tgcagttt   6300

agttttgttc cctctccctt aatctcttta tcaaataaga aattcagcca aa

#aatatatg   6360

ctacactgaa atatagttat aaaaatgcaa acaaagaaca acatgctata tc

#tgattcaa   6420

ttctaacatt tactgacaat aagaattgtg acttgatgaa agattttgtg tt

#taaacttt   6480

acatctacct gctaggctga tccaaactct cttagaattc tatgtgtgca ga

#ttctttgc   6540

ttctctgtat tacaccaact actttattca tgactgaaag attactagga ct

#ttgggaaa   6600

atttaacagc aacttaaggt ctttcttgtt tattgtttaa gactaaaatt aa

#ggggtaaa   6660

aaaaagcctt tctttaaagg cttaaaaaaa ataatagggg caaatttacc ta

#gcatagat   6720

ttagtgatac ttagtcatca aaaatgtcca agacaaaaaa ttttaccgaa ag

#tcaaacac   6780

aacttgtttt taataatttt atttcttggc atttttattc tagatgaaac ac

#taaatgaa   6840

atatattata aatagaatgc tacatatata agtagaacaa ttcaagttcc ca

#tttgatag   6900

agtataatat tttgaattgc tggtgattat ttaatgtaaa aacatttatc tg

#cttaaaat   6960

tctcaataaa cttcaaagag aagtgagtaa tatgatattt ggattaaatt ta

#catgctta   7020

aatatggcat tttattacat ctctgaattt cacttctctt ctctgaagaa at

#ttcctcag   7080

tgtgctgctg tttcccccaa attggcagag tcagttgaat ctcagaataa tg

#caattttt   7140

aaaaacaaat atacaaaatc ctacaatgtt ctagaaagaa ttgtactggg ca

#aggatata   7200

aaagtctgta ggtctctgcc ttcaggaggt cacaggtaat gggttgtaac ta

#caaaatac   7260

aagtaactat ggcagaatat gaaagtagtg aatgccatga ggtagtcttg aa

#gactggcc   7320

aacatagaga gaaaaggtca tttcaggcag aggaaacaac atcattaaag gt

#agggaggc   7380

agaaagcaaa taatagaata gttcattttg gctatagcct agtgggataa ct

#tagactta   7440

ccacaggaaa ggtttgttgg gaccagataa gtgtagaatc ttgaatgcta ga

#ctatgatt   7500

tctaaactga gaacatttct ttgctgatgt acgtattcct ggaaaaaata aa

#ataaaaaa   7560

aacaaaagag cagtacctat attttgaagt cattttcaga gctctaaccc tc

#ttgagact   7620

ttgagaatga aaattaaatt cctgagtaga tttagtagtt agtagacaag gt

#agggggta   7680

gaaacaaact gaaggatttt aataaaattt tctatcaaaa ttgcacatga ga

#gcatttct   7740

cagtctatcc acaagcactc aaaagtccta gatttcagat cctaagagac ct

#cctgcttg   7800

tccgtgatgt aaactccatt ttattggtac gtaatctgat ttagctttgg ct

#ttgttttt   7860

gacatttcct aaagcaagga caatctagtg ggatcatttt aatacaatga at

#actcatgt   7920

tactatggtg aatagttgga taaaaaggac tttgtcttag ggaaaattgg aa

#attaaaat   7980

tgccattttg aatcacggaa gtcgctgaat attttacctt tgttctctgt tc

#atttaaaa   8040

atcataaagt aaaccatgtt tgcaaatact tttaatatcg ccttcttcta ct

#ccatacac   8100

cagaggcatt ttagtattgc atgaggttag taaaaaagct ggataccttc ca

#agagcaga   8160

tttcctttag atgtgacagc tgggatgtga cttttggtat cagatgcagg aa

#gacgtcat   8220

ttgtacatgg taattgtgaa aaaattggaa cttattactc tcagtataaa tg

#atccataa   8280

aaagtatgtc agaagtaaaa ctcctggaat tctacaggga gagttaaaat aa

#aaccagac   8340

acaggtgctc atctgactct atttttagaa caataggaga ctcatataac tg

#agaatgct   8400

ctgtacttcc tgtataaatc tacattattt gaaagtcgta ttttctagaa gt

#tcctgtga   8460

agttgtactt attaatcttt gcaacttcac attgcctagg aaagagccat tc

#acctggta   8520

ggaacccaac aaattttcag tgcttgtctt agaatcatag tcccatttct ga

#aagaaacc   8580

ttgaatatca ttgggcttca agttgttcta aaaatgttta agcatttaaa ca

#tggttttc   8640

tttctcaaaa agcaaataga aggcatttag aggaaaagga ccctttcttc ac

#cttaagac   8700

ttttaaaaat ggcaatatgg gaagattaat aagaagaata agttaaggga ga

#attcaata   8760

ttcctccatg aaactactct ttctaaaagg caacagagac tggttccagt ga

#agcatatt   8820

atgatgtgtg gcgtgtaaat gtatatcatt atccctactc atctttttcc cc

#aaattcaa   8880

tttaatactc ataagaattt attgaggcta ctgtataaca tggaggaaag ct

#gtatacca   8940

cagtagcaag gagctagggc tccagagcgg gactcctgtg ttatgatccc at

#atcttcca   9000

ctttactggc aatttttatc ttaggaagtt acttaatctc tcttttcttc ag

#tgttttca   9060

tctgtgaaat gaggacacta atacgttaat ctctagagtt gtaatgaaaa tc

#aaataaaa   9120

taataaatta atacttcaaa cagtgcctag agtgtttgat acagtgccta gc

#ttttggtt   9180

attataatta tccccactga actaggtaaa tgctacaaat atgtatgtgt at

#atttgtgt   9240

gtatacacac aaatatgcat atatgtacac acacatactg tacatcctat gt

#aaacacaa   9300

ttttagtatg tatgtatgtc tatacatacg tatacattct accttaagta ta

#tatagtat   9360

actgaaaaag aaatttagta gtttgcccaa gatcaaaatt gcctgcaaag ga

#taggacaa   9420

tttgagtttc aaacccagaa agtctagctc tacagctgtt ggccttaact ac

#tgtttcat   9480

actgtttaga gtataaacac ctgaattaga tagccatgta taaattagca ta

#ttctaaat   9540

gccaaattga gactaaagac atgaaggtaa actgaaacta ctgtgaaaga ct

#taatggaa   9600

gaattgtgac ttttatttga ttttaagttc tgggatacat gtgcaggata cg

#caggtctg   9660

ttacataggt aaatgtgtgc caaggtggtt tgctgcacct atcaacccat ca

#cctaggta   9720

ttaagcccag catgcattag ctatttttcc ttatgctctc cctcttctca ca

#cacccctc   9780

agcagacccc agtgtgtgtt tttcccctgc ctgtgtccat gtgttctcat ct

#ttcagctc   9840

ccagtgagaa catgtggtat ttggttttct gttcctgcgt tagtttgcag at

#gataatgg   9900

cttccagctc catccatatc cctgtaaaag acatgatcta attcctttct at

#ggccacat   9960

agtattccag ggtgtctatg taccacattt tctttatcca gcctatcatt ga

#tgggcatt  10020

tgggttgatt ccatgccttt gatattgtta atagtgctgc aatgaatata cg

#cacgcatg  10080

tatctttata atagaatgat ttatattcct ttgagtgtat acccagtaat ag

#ggtcaaat  10140

ggtatttctg gtgcaggtct ttgaggaatt gccacactgt tttctacaat gt

#gtgaacta  10200

atttacattc ccaccaaaaa tgtaaaagtg tttctgtttc tccacagccc tc

#gctagcat  10260

ctgttgtttc ttgacttctt tataatcacc attctgactg gcatgagatg gt

#atcttatt  10320

gtggttttaa tttgaatttc tctaataatc agcaatatta agctttctct aa

#atatgttt  10380

tttggctgct tatatatctt cttttgagaa gtgtctgttc atgtcctttg cc

#cacttttt  10440

gatgggtttt ttttttttct tgtaaatttg tttatgttcc ttgtagagtc tg

#gatactag  10500

gcctgtgcca gatggatgga ttgcaaaaat ctcccattct gtaggttgtc tg

#ttttctct  10560

gatgatagtt tcttttgctg tgcagaagtt ctttagttta attagatccc at

#ttgtaaat  10620

ttttgctttt gttgcaattg cttttgatat ttttgtcatg aaatctttgc cc

#gtgcctat  10680

gtcctgaatg gtattgccta gattttcttc tagggttttt ataattttgg gt

#tttacatt  10740

taagtcttta ctccatcttg agttaatttt tgtaaaagat gtaaggaaaa gg

#tccatttt  10800

caattttctg cactatttat taaataggga atcctttctc cattgcttgt tt

#ttgtcagg  10860

tttgttgaag atcagacaat tgtaaatgta tggtcttatt tctgagttct ct

#attctgtt  10920

ccattggtct atgtgtctgt ttttgtacca ataccatgct gctttggtta ct

#gtagcctt  10980

gtagtacagt ttgaagttgg gtagggtgat gttgccagct ttattctttt tt

#ctttagga  11040

ttgtcttgac tataccagct cttttctggt tccatatgaa ttttaaaatt tt

#ttttctaa  11100

ttctgtgaag aatgtcattg gtagtttaat cattgaatct ataaattact tt

#gggcagta  11160

tggccatttt catgatgttg attcttctta tccatgagtg tggattgttt tt

#cgatttgt  11220

ttgagtcatc tctgatttcc ttgagcagtg gtttgtagtt ctccttgaag ag

#gtccttca  11280

cattccttgt tagctgtatt ctaggtattt tattctcttt gtagcaattg tg

#aatgggag  11340

ttcattcatg atttggcttt atgcttgtct gttgttggtg tataggaata cc

#tgtgattt  11400

ttgcatgttg attttttatc ctgagatttt gctgaagttg cttatctgct ta

#agaagctt  11460

ttgggctgag atgatggggt tttctaggta tgggatcatg tcatgggcaa ag

#acaatttg  11520

atttcttctc tttctatttg aatacgcttt atttatttct ctttgcctga tt

#gccctggc  11580

ccagaacttc caatactatt tgaataggag tggtgagaga gcatccttgt ct

#tgtgccag  11640

ttttcaaggg gaatgcttcc agcttttgcc catgcagtat gatattggct gt

#gagtttgt  11700

cataaatggc ttttattatt ttgaggtatg ttccttcaaa cctagtttat tt

#agagtttt  11760

taagacgaag ggatgttgaa ctttatcaaa gtccttcttc tgcatctaat ga

#gataatca  11820

cgtggctttt ttctttagtt ctgttcatgt ggtgaattat gtatattgat tt

#gcatacgc  11880

tgaaccaccc ttgcatccca gggatgaagt agacttgatt gcgatggata ag

#ctttttga  11940

tgtgctgctg gattcatttt gccagcattt tcttgaagat ttttgcattg at

#attcatca  12000

gggatattgg cctgaagttt tctttatttg ttatatctct cccaggtttt gg

#tgtgagga  12060

tgacgctggc ctcataaaat ggtttacaga ggagtccctc ctttccaatt gt

#ttggaata  12120

gtttcagaag aaatggtacc aactcctctt tgtacctctg gtagaattca gc

#tgtaaatt  12180

catctggtcc tgggctgttt tgtttgggag gctattttta ctgcctcaat tt

#cagaactt  12240

gttattggtt attggttatt gattattctt cagggaatca acttctttgt gg

#gtcagtgt  12300

gaggagggtg tatgtgtcca ggaatttatc catttctcct agattttcta gt

#ttgtttgc  12360

atagaggtgt ttatagtatt ctctgatggt tgtttgtatt tctgtgatat cc

#cctttatc  12420

atttttactg tgtctatttg atttttctct tttttcttct ttattagtct ag

#ctagtggt  12480

ctagctattt tattaatttt ttaaaaaaat cacctcctgg attcgttgat tt

#tttgaagg  12540

gtttttttgt gtgtctctct ccttcagttc tgctctgatc ttgcttattt ct

#tgtcttct  12600

gctagctttg gggtttgttt gctcttggtt ctctgtaaat agttctttca gt

#tgtgatgt  12660

taggatgtgg gtttgagata ttgctagcat tttgatggca gcatttagtg ct

#ataaattt  12720

ccctcttaac actgctttag ctgtgtccca gagattctgg tatgctctct tt

#gttctcat  12780

tagtttcaaa gaacttcctg atttttgcct taattatttt attcacccag aa

#gtcattca  12840

ggagtgggtt gttcaatttc catgtagttg tgtagttttg agtgagtttc tt

#aattttga  12900

attctaattt gattgtgcca tggtctgaga gactgttgtg atttcagttc tt

#ttgcattt  12960

gctgaagagt gttttacttc cacttatgtg atcagtttta gagtaggcac ca

#tgtagtgc  13020

tgagaagaat gtatattctg ttgtttttgg gtggaaagat ctgtagataa ct

#atcaagtt  13080

cacttgatgc agagctgact tcaagtcctt tgttgatttt ctgtcgtgat ga

#tgagtcta  13140

atattgacag cagggtgtta ttatctccca ctgttttttt tattattata ct

#ttaagttt  13200

tagggtacat gtgcacaatg tgcaggatag ttacatatgt atacatgtgc ca

#tgctggtg  13260

tgctgcaccc attaactcct gcttgagcaa tagtggtatc tcctaaggta aa

#ctttcccc  13320

ctcccctaac ccacaacagg gcccaaagtg ggttggtccc ccttcttnnn nn

#nnnnnnnn  13380

nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nn

#nnnnnnnn  13440

nnnnnnnnnn nnnnnnnnaa tatatgtggc tccatcttgg ttcacactgc ta

#ctcagtgt  13500

actacaaatc acagtgagtt tgaatgccat tcatattact gcaaacgaca tt

#ttatttat  13560

ttttattgcc agtgcatatc catcatgcca gaacaagaaa ataagagaaa aa

#tgaacttt  13620

gattgtcatg cttttatagc acagtggagt gtgaattatt ttatttaatt ag

#atgacaaa  13680

atatgtattt attatgtaaa gactctatag ctatgctaaa agaatagaat at

#atctccac  13740

ataaccagat taatcactca tcacaatatt cctgactcac aagaagacaa ca

#gtcataaa  13800

tattagaagg cttaaaatgg aatctctcat tatagcagag ttttcctaca aa

#acaaaaag  13860

gacagtgaga cttcaaccaa tgtacatttc tgaatggctc acttgttagc ca

#agtatgcc  13920

cttataagac tgtggcactc taaacagggc tttcacaatg tccacccaca ca

#atacctgc  13980

cttaatgaaa agctcagtac cagtttcagg caatttaaaa atcttagcct tt

#attatatt  14040

gaaattaagt cgaattattt ttctattatg atcccttttg aaataagctt tt

#acacattt  14100

ctaatgcttt cttcagagcg gctcatataa atcaatgatt ttttaaaaaa tt

#ctttcatt  14160

tcgatttaat ctattaatac tttagatctc actctcaggg aaaaattact tt

#attgcatg  14220

taaagtaatt caaatagaat atagtttaca attttcttcc aaattaagct tg

#agcctgga  14280

taaaaatatt tttaagtgcc caacaatatt tagatattat ttgccatgtt tc

#tattttca  14340

taggaagaga taatatgttt aataaaaaat acatatctaa aaggataatc tg

#atgttgta  14400

aaattataaa ttctaatttt ctgtcaaaac aaccctgaat gtgaacttat ca

#gaatcttg  14460

tctgtgtgac tgcaacccct cccccaacct taaaaaacat accaccagcc cc

#actctcca  14520

ccagtgtggc caaaccaagg gaagtgagaa gcaggaacat agctacacag gt

#cagagcta  14580

aatattaaga gtaaaaatag tatcttgagc tttcagaacc acaaattttc aa

#agtgagcc  14640

agaggacaga gcagcagctg cattttcaaa cagaagcaac tacatttttc ta

#atcaactg  14700

ctgtgttatg gaacatgaac tgcaggaaat gatggactaa tgtcctttta tg

#tatcagat  14760

aagcaggagg aagtatcagt ggtgtgcttt acttggtgag tgaatcttga ta

#aacatatt  14820

caataaatat cttccactta tgtcctttaa ttcagtacaa tgctttttaa aa

#aatattca  14880

acttgtgtgt acatcgacca gaaaatgttc tatataaaaa ctgtattttg ct

#tgggtttc  14940

gagatgaatg tttcataaga tatctatata tgtattaaaa ttatttaaat at

#gaggaaaa  15000

agaacttgtt tgctgttggc gatgaaatca tgtttaatta tagtactgaa aa

#aaatgtgc  15060

caagagtaaa caaacttgtt tagtgctgct agtgtttagg tgagaaccat tg

#cttgaaga  15120

gttggggaca ctgggagcaa catagatggt caatgaaaaa atgacagaag ac

#tgatgtca  15180

ccaaagtgtg gagtaggaaa ccttcgtccc caccacaaac acaccaattc ag

#gaacaatt  15240

cacagaaaaa ttccctttgt gggaaatcca gcaactaatt gaagggctcc tg

#caccctgg  15300

gtgaatgcaa aatcagatcc atcgaagctg gtgaggatat tcacgacagc tg

#tctgccaa  15360

aatttctacc cccaacgcaa caccatacaa ttgggaaaag agtctcagct ct

#cagcttct  15420

cccagaggag gtttgtacat ccaatacccc aacttcgatg ggggctaccc aa

#aggactgg  15480

cttctgtctt ctctgtctta aagtgctaat ggtgtggaat tatctagcca cc

#tgggggag  15540

aatagagatg gtggcttaga ttggtagcca ccatagcttt tcctccctag ct

#cagagcat  15600

agagcaagca aacaaaatcc ccacctttca gcttctccct ggggatggaa ag

#agttggta  15660

catacattaa actttctggg ggttttccaa aggattggct gaaatcccaa ag

#aattcagt  15720

ctcactcatc ctggtgcact cacaagacct ggcaaaccct agacacctgg gg

#ctacaaga  15780

aatacacaag caaataagtt gaacaagcat gaggtttaag aagctttaga at

#ctcttcct  15840

ggacttattg gtggggatct tccatataag gccagctctt tgtgaagact ca

#gagagaag  15900

tctgctttat ctgatgcaaa gacaccaatg catagagtca agtaagatga aa

#aaacagga  15960

aaatgtgttc caaactaggt aacagaaaaa tctccagaaa ttgactctaa tg

#aaacaaag  16020

atacacaatt tacctggaaa agaatttaga ataactgtca taaagatgct ca

#ctgaggat  16080

aagagaacgt tgcatgaaca aagtgagaat ttcagcaaag agatagaaaa ta

#tcttaaaa  16140

gtaccaaaca ggaatcatga agttgaagaa taaaataatt aaattgaaaa at

#tcactaga  16200

gggattcaac aacatactag tatcaagcta aagaaagaat cagtgaactt aa

#ggacaggc  16260

cattggaact tgctgagtca gagaaacaaa aaggacaaaa taatgaaaaa ga

#ataaaaaa  16320

agcttaaagg acttacgaga caccatcaag tggatcaata tatgcattat ga

#gaattcca  16380

gaaggagaag agagaaggaa agaaccagaa gatttattca aagaaataat ag

#ctaaaaac  16440

tcccaagtat ggaaaaggaa atgtgtaatc caaggacccc caaaaaggaa aa

#cttagaga  16500

tatcaacact aagacacctt ataatcaaat tgtcaaaagt caatcacaaa ga

#gaaaaagc  16560

aacaagggaa aagttacttg ttcgggtaca agggaaattt cataagagta ta

#agtagatt  16620

tttcttcagc aacttttttg cagatgagaa ggaaatgaga tgatagattc ac

#aatgctgg  16680

gggaaaaagc caaccaggaa acctagacca aatgaaactg tccttcaacc ag

#gaaaacta  16740

gaccaaatga aactgtcatt caatcatgaa agagagataa agtcttttcc ag

#acaaacaa  16800

aaactaagga agttcatcac caccagacct ccctacaaaa aatgctaagg ga

#acctcctt  16860

aacttgaaat gaaaggacac taaacagcaa caagatagca taagaaagta ta

#aaagtatt  16920

ggtaaaggta aatatataga caaatgcagg accgtaatac tgcaatagtg gt

#aggtagac  16980

cacttgtaat tcaagtaaaa aagttaaaag acaaagtagc aaaatacttt ca

#ataactaa  17040

aatactttta ataagtaaaa ctatgttaat agatacacaa tataaagaaa tg

#ttaactgt  17100

gacaacaata acaaaatgtg tatgggaagg agagtaaaaa gaggcatatt tt

#tgtatgtc  17160

attgaactta agttgttatc aggaaaaaat agactgtcat tactataagg ta

#ttatataa  17220

accccatggt atctaatgag aaaataccta tagaaaggta tcaaagattc cc

#aacaaaaa  17280

aaaatcaaca aaacatgaaa aatgagagca agagaggaaa aaatgcacaa aa

#taattaca  17340

aggctaacag aaaacagtac atgacaataa taaatccttc tctatcaata at

#tactttaa  17400

aactaaataa attatacttc ccaatcaaag acatagggtg gttgaatgga tt

#aaatgtat  17460

aatggaatca catgctgtta tcaagagact ccctttagaa tttaggctca at

#gtgaaaga  17520

atggaaaaaa aaattccacg aaaatgttaa tgaaaaacga gcaagagtga ct

#atacttat  17580

atcagataaa atagactata agtcaaaact ctctcaaaag actgagaaag ac

#atcttata  17640

atgataaaag gatcaattca ccaggaatat ataacaattg taagtagtta tg

#cacccaac  17700

gattaagcac ctaaacatat aaagcaaaca ttgacaaaac tgaagagaga aa

#caggcagc  17760

aacacaataa tagtaggata tttcaatacc tcattttgaa tgatgggtaa aa

#catattat  17820

ccattaccca cgggcaaaac agagcaaaag gaaataaagg acttcaacaa cc

#ttatagaa  17880

aaaaatggac ccaatagaca tgaacatttc actcaatagc agcataatac ac

#attcttct  17940

caagtgcagc cagaatattc tccagaatag atcacatatt aagctgaaaa gt

#atgtttta  18000

aaaatttaaa gtgatcaaaa ttgtaccaac tattatttct gactacaatg ga

#atgtgaaa  18060

gtagaaatca atagccatgg gaaaactgaa aatattataa atatgtggac at

#taaacaaa  18120

acactcttga acaactaatg ggtcagaaag aattcaaaag agacattaga aa

#atatcttg  18180

agagacatga agatgaaaac ataatatacc aaaacttatg gtatacagcc aa

#agcactat  18240

taaaagataa gtttataatg ataaaagtct atatgaaaaa agaagacaga tc

#tcaaattt  18300

gcaacctaat tatacatttg aagggactag aaaaaaaaaa cacactagac cc

#aaagttag  18360

ctgataggaa gaactagcaa agatcagagc agaaataaac aaaatagata at

#agaaaaca  18420

ataggaaaaa atcaatgaaa ttgggttttt ttttaaaaga taaaattgac aa

#acctttgg  18480

ctagacttag aaaaaagaga ggattcaaat aaatataaat catatattaa ag

#aggaggta  18540

ttaccactga tatcacataa gttaaaaagt tcataagtat ctatgataaa ca

#attatatg  18600

ctaagaaact ctatgacctt aaaaatggat aaattcctag gaacataaaa tc

#taccaaac  18660

acgaaacaag aagatataga aaatctggac agacaaataa caagcaagaa aa

#ttaaatca  18720

gtaataaaag acctccaaac aaagaaaatc ccaggaacag atggcttcac tg

#gtgaattt  18780

taccaaacat ttgaagaaga tttatgtcaa actttttttt atcttgaaga ag

#aggaaata  18840

cctccaaact cattgtatga tgccagcatt accctgatac caaagccaga ca

#aagacact  18900

gcaagataag aaaattacat aataatatct ctgatgaaca tagatgcaaa aa

#ttcttaac  18960

aacaaaaact acctagcaag ctgaattcaa cagtacatta aaaagtcata tg

#atatttat  19020

tataggaagc aatggatacc ctgggctggg gttcattata tacaaatcaa ta

#aatgtgat  19080

gtgccacatt cacagagtaa agaacaaaaa atatattatt atttaacatc gt

#ttcatgat  19140

aaaaactctc aacaaattag ctgtagaagg gatgtagctc aacacaataa ag

#gccatata  19200

tgacaatcct acagtttaca tcatactcaa tgatgaaaag ttgaaagctt tt

#cctctaag  19260

ttcaggaaca aggcaaggat gtctactctt gctacttcca ttcaacatag ta

#ctagaagt  19320

cctaggaaga gcgattaggc aagaaaattt tttcatgtgc agatgagaaa aa

#atgtatat  19380

tctgtggtcg ttgaatggaa tgttcagtag atgtttatta ggtccatttg gt

#caagagtg  19440

cagtttaagt tcagagtttc tttgttagtt ttctgcttta atgatctgtc ta

#gtgccatc  19500

attgggatgt tgaagtcctc cactgttatt gtatatctgt ctgtctcttt tc

#tgaggtct  19560

aatggcattt gctttataaa tctgggtggt caggtattgg gtataaatat at

#ttaggata  19620

gttaaatctt cttgtagaat tgaactcttt gtcattatat aatgttattc tt

#tgtctttt  19680

ttttaactat tattggtata aattctgttt ttttctgatg taagaatagc aa

#cctatgct  19740

cttttttgtt ttccattgtg tgatatacct ttctccactc ctttactttg ag

#cctgtggg  19800

tgtcctttca cattagatgg atctcttgta gtcagcagat gttgagtctt gt

#ttcttaaa  19860

tgcaatttga caatctatat cttcatttag gtcatttctg ttcaaagtta at

#attgacat  19920

gtgaagtttt gttccaatca tagtactgtt agctaattgc tttgtagtct ca

#gtggtgtg  19980

attgctttat aggatctttg gattttgtac ttatatgagc ttttatgaca gg

#agagtatt  20040

gtcctatatt cttttatgac ataaaagagt atactctttt ctgttcgaag tt

#tatgcttt  20100

atgacataaa agagtatact catttctgtt caaagttaat attgacgtga aa

#ttttgttc  20160

caatcatagt attgttagct agttgctttg cagtctcagt agtgtaattg ct

#ttttagga  20220

tctttgagtt ttgtacttat atgagctttt atgacaggag agtattgtcc ta

#tattcttt  20280

tatgacataa aagagtatac tcttttctgt tcaaagttta tgctttatga ca

#taaaagag  20340

tatactcatt tctgttcaaa gttaatattg acatgtgaag ttttgtccca at

#catagtat  20400

tgttagctag ttgctttgca gtctcagtgg tgtaattgct ttataggatc tt

#tgaatttt  20460

gtacttatat gagcttttat gacaggagag tattgtccta tgttctttta tg

#acataaaa  20520

gagtatactt ttttatgaca aagagtattg tcctttttcc ccacgtttac aa

#cacctttg  20580

agcatttctt atagcaccag tctcatggtg atgaattttc ttaatatttg ct

#tgtttgag  20640

aaagacttta tttctccttt gcttatgaag cttagttagg caggatatac aa

#tttggggc  20700

tataattttt tgtcctcaag aaggctaaaa ataggccccc tatctttttg gc

#ttatatgg  20760

tttctgttga gaaagccact gctagtctga tggaatttcc tttacaggtg ac

#ttgactgt  20820

tctctctaac tctctttaag attttttctt tagcattgac cttggttagt ct

#gatgacta  20880

tatgccttga tgatgttcat cttatatagt atcttgcaag tgttttctga at

#ttctttta  20940

tctggatgtc tacctcccaa caagatcagg gaaatttttc tgaatgattc ct

#ttaaatat  21000

gtttccaaat tgcttacttt tccttctttc tcagcaatac ctataagcta ta

#ggtttggt  21060

caatttaccc cctataccat ctttctcaaa tattttgttt atttttaaaa tg

#cttttcta  21120

tttatttttg tctgactgga ttaatttgaa agaccaatgt ttaagctctg aa

#attctttc  21180

ttctacttgg tctagtcttt tgttaatgtt ttcaattgta cattgaaatt ac

#ttttgtga  21240

atttttttat tttcagaagt tctattttta taaatatagc tatcttgtct tt

#cattttct  21300

gagttgttct tctggtttct ttgtattggt tttcaacatt ctcttggata tc

#attgcact  21360

tctttagaat ccgtatcttg aattccttat cagtcatttt ttattttgtt ta

#ggatccat  21420

tgctagaaat ctagcctgat cctttcaagg tgttaaaaca ctctgtcttt tt

#gtaccact  21480

ggagttcttg cactgattcc ttcccatgcg aaggagttgt tgcttctaag tt

#ttgaattt  21540

gctattgttt gaatgggact ttatcatgtt tattcttttt tcccttgagg gt

#atgactgt  21600

ggtgtatgtt gtatgtgatt gtttggcttc ttttctgggg tttctcggtg cc

#aagactct  21660

gcatgggctc cttggttatg gatagccttt gtgtggtggc tttctcaaat gc

#tgcttgtt  21720

gtagacatgt attgggcata tgagccaaca cactattttc tgtgtgacta gg

#agagcaga  21780

ggtctcagta aacttatctt gtacactagt actataccct tctgacagta gg

#ttttttat  21840

ttggtggtgc aattcagtct tcagtcaagt aggaggtgct taagagtaag aa

#tccactca  21900

ccctcaggca gtctaatgat gaaggaagac aactgtccta attgaggtta gt

#gtggggag  21960

cttgtgttgg agtgaactgg tcttggtggt aggggcaggg ggcctgcatt ag

#cccctcat  22020

cctgggcagg caggaatgtg atccgttttc ctatcacacc tttctgtcac ag

#ggctcatg  22080

atcttcagca tatagacatt gttctttggc tcccaagctg aagtgtgact ga

#ggtctgga  22140

gaaatgcccc tttggtggct accaccaaaa tgagctcagg gcagagcctc tt

#cccagagc  22200

ccagagcaaa cagtttttca acttgtctgc ccttcgttgc tgggacactg cc

#attctgtg  22260

ttgggatggg gagacaggtc ccacctttca tgcatgccta ggtggcattg gc

#tcactttc  22320

aatgaggtgt agctgccacg aagagtgctg gaaaggctgt ctccaagtgc aa

#tcaggtca  22380

gccctcatca ggaaaaagcc tctgctgcat ccacaacagt gcctgcactg ag

#ggctagat  22440

ttccatggaa cctgcagctc cccagagacc cgccagtctc ctgtggttgc ca

#aagtcaga  22500

aggggttctg aggtatgttt gcaggggatc ttgtagtgtg gcaacacaag ga

#ctaaggtt  22560

ccttggacag ggcactggcc cacaatgagt gcacaaccag tgtggcacct gc

#catctcag  22620

ttagggcctg aggggagtgt gggcacacca gcacgagctg gccacctgag gc

#tcccaccc  22680

cagagagttc ccaaattgcc accaactgca ttgcctggga tttcaagggc ag

#aggggttc  22740

tctgacaatt tgtcagtcag cagttagtca caggagtgag gggagcagag aa

#gcacccca  22800

acctatcctt tacatgggac tctgagttcc tcaggagtca gtgtctgcca ga

#cttttgct  22860

gctttccttg tctgcacccc agtttcttcc catgggctct ctgaaagctc gt

#ggctctct  22920

tccctcagct ttccatttgg atcatgacca ttcaactgta actttgatct tt

#ctacaaac  22980

tggtgtctga catctctagt cagccatctt gaaaaaaaaa agctacatta aa

#gttataaa  23040

aataaaagta attgcactgt gatgttacaa aggctactat atcactaggt ga

#caagaatt  23100

tttcagccct attatagttt tatggtacca ctattttata tgcgatccat ca

#tttgactg  23160

aaacatcatt atgtatgact gtacataaca aattgcgaat agaattagaa ag

#tgctttct  23220

acttctggaa atcaatgttg tcttcacaga gacagaggtg ggctttgaag ga

#taaatagg  23280

agttcaggag gcaaagaagg aaggatctgt tatattctgg gaatggcaaa ta

#tgatgtgg  23340

ataaagcatt gggattgtgt ctgggggcat aaaatgtgac tggatataaa gt

#ttaaatct  23400

ttacataagg taggtcaaat tgtggagaat gaattaatcc ttgaagtcac tc

#tatctgat  23460

aagcacatta ttatctccat ttcacagata aagaaactaa ggtacagaag at

#taaatgac  23520

ttaaataggt cacctgacta gtaagtcgta tggcagtgat tcaaacccac aa

#ggaagact  23580

tgtacatatt tattgacttt ttcatgatga tttttaaaaa gttgagaata tt

#ctattata  23640

aagcaataaa gaatttgata tttagtaacc atatcacaat agttttacaa at

#gttttagc  23700

aaaagtttga aagttttata gttagaaaat tcccattgaa ctaagattta tt

#cccataat  23760

taggaaagcc actctcccat tggagactac ttttattata gcctcatgtt ct

#cttacttt  23820

aaattatctt ctctgctgta ccacaaaata aaaagtctta taatttcctt at

#ttcaaatg  23880

ttttttcttt gaaaaagaac catttatttc tggtattatt agttgattaa tt

#tttgtgca  23940

acttagtagt gttgatatag gatcaatgtc aactggtgga gcaattctaa gg

#gtgtttgc  24000

tccattagta ataaccagtg gagttaatta attacacagg catttgaaat tg

#taggtttt  24060

gcctgttaaa cactggatat ttcaggatga gaaatgtgga ggtggactaa ta

#ctgaacat  24120

tttatttcag aaaatacagc caatagtaaa tttcagtctt ttattgagct at

#ctttgaca  24180

cctgtgcaca tcttataata aactgttctg tttttcaatg ggtatcctag ga

#acaagaac  24240

taaataagag acaattattt taaagtcttc aataatagaa tttacttttg tg

#tgggcaaa  24300

agacacgaac agacacttct caaaagaaga catacatgcg gctgacatag ga

#aaaaaaag  24360

ctcaacatca ctaatcatta gagaaatgca aatcaaaacc tcaataagat at

#catctcac  24420

atcagtcaga atggctatta ttaaaacgtc aagaaacaac agatgctggt ga

#ggttgtgg  24480

agaaaaagga ttcctttaca ctattggtgg aaacgtaaat tagttcaacc at

#tgtggaag  24540

acagtgtggc aattccttaa agacctagag gcagaaatac catttgaccc aa

#caatgcca  24600

ttaatgtgta tatacccaaa ggaatataaa tcattctatt ataaagatac at

#gcacgcac  24660

gtgttcattg tagtgctatt cacaatagca aagacatgga accaactaaa at

#gcccatca  24720

gtgatagact ggataaagaa aatgttgcac atgtataccc tgaaatgcta tg

#cagccata  24780

aaaaggaaca agatcatgtc ctttgcaggg acctggatgg aactggaagc ca

#ttaccctc  24840

agcaaactaa agcagtaaca gaaaactaaa taccacatat tctcacttat aa

#gtgggagt  24900

agaatgatga gaacacatgg acacatgaga ggaaacaaca cacactgagg cc

#tgttggag  24960

ggtaggaggt gggaggaggg agcacatcag gaagaatagc tgatggactc tg

#ggcttaat  25020

acctagatga tgggttgatc tgtgcagcaa accaccgtgg tacacattta cc

#tatgcaac  25080

aaaactgcac atattgccct tgtacatctg aacttcaaaa taaaagttgg ag

#attaaaaa  25140

acgaaattac ttttgttcca gaattaactc tcagatgttc catgtttcat ca

#ctttattt  25200

tttcacataa tttgtgtatg tgactcacat caattcattt tgatatataa tt

#gatttctg  25260

atattttgtt tgtttgaagt gagaggtaac tgggtaatta tctatactct gc

#ttttacca  25320

tgcattttat ttccaggtaa atttgaaaaa tctaaattat ttttctaaat tt

#gatcatgg  25380

tttatttgac agtttacaag tacttgcagg catgtgtttg catgtggata at

#aacaaata  25440

actaagaaat cttacaaaag tatagcttca taatttgggg gtcctggtta ta

#cattttac  25500

atctctaagt taggaactca tattgttaat ctcccttcat agttccttat aa

#ctaaactc  25560

tgtttagtat gagtttctac ttatcaaagg cataataact cactcactat tt

#ggtatatt  25620

tgctctttaa tgtgacatga catgttttct gtggataagg agaactgtgt at

#ttgtgcgt  25680

atatgtatat ataatgtttt caaccaatca ctatttcaga gaaaaaatgg at

#gaaaataa  25740

acttgtattc attacattaa atataatcct atacatatta agaggaaatt tt

#acagcagg  25800

aaattgttcc tttaatcatt atttttcttg aaaattattt aatactttta ag

#acaaacca  25860

cggatgacca aagtctctta atatttacca catagattta tattaacact at

#atttttgt  25920

tttaagtttt ctagacatct gagacttaaa tatgttctta tttaaagact tt

#aatagtat  25980

ggcagttgta ccatgaaggt ggcatagtga aggagatcaa cttagtctac tt

#tttgacta  26040

aattcttaaa tctctatttc agctgtcttc cccctagaac tatagcttaa aa

#gctcctca  26100

gctgcataca gcacatagcc ttcacaggtt atcgcctttc tatagagtcc tc

#tcacaata  26160

taaacaggtg tagctaccaa ttaggacatg tctcaagaaa ttgttaacac tc

#accaatat  26220

taattaagtg ctaatagggt actgagccaa acactgaggg tgctgagcca aa

#tttccatt  26280

tcacattctt cattctccaa ggaggtttag atactggtgc tgtcaatagg gt

#gcttgagt  26340

tctagaaccc atggggaaaa ataaattact gtggccactt tgcacataaa tg

#tttaaatt  26400

taaaatatca attgatataa atactgataa taatgaataa atattaaata at

#aattgaaa  26460

gggatgatgt tcttggtttg ggggataata cccataatct tagcagtacc ag

#aatcattg  26520

caaccctaat aggattaatt ccattttgga atatcagtat tctgagatta ct

#attttgaa  26580

tgttctcgtt tatattttct tcaagtaaac ttttttgctt cttcattctt tt

#tcagaaat  26640

tttattattt ttaaaattga cagataaaat tgtatgtatt tattatgtac aa

#catgatgc  26700

tttgaaatat atatatctat gcactgtaga ataactaaat atagctaatt aa

#catatgcc  26760

ttacctcaca tagttattat ttttgtagtg aaaatactta tccactctca ct

#atttttca  26820

ggaatacaat atgttattaa ctattgtcac tatgctgtac aatagatctc tt

#gaacttat  26880

ttctgctgtc aaactagaat tttatatcct ttgactagcc ccttcctcag cc

#ccccaagt  26940

gccccagccc ctagtagcca tcattctact ctctagttct atgtgtttgc ct

#cctcgttc  27000

tatctttcct cttcctcact acctagtcat tcctagtgcc cacagtgtgt ca

#caactgct  27060

gaaagcatgg tgaaaaaata tctgttttct tttcttccct tctctctctc tt

#cttaatgc  27120

gtttcaggtg ggaagataat aaaagaaacc aaaatgattg aaatcattat ta

#gcagaaag  27180

taaaatttta atttcctgct ggtacaataa gcttttgtct gggctctggg ga

#caaaaaga  27240

ttatgaatat tcttttgtgc cactttcaaa ctgcttctaa atatcttagg ta

#catttgta  27300

atatgaaaat atggcagcct tattagcaaa ataatttcta attttgagct aa

#attgtata  27360

agattatgca tgtttttctt ttgcataact caatttgttt cctgtaatga ta

#attgccat  27420

gattgaatta gaagataata tagcataaaa aaattttatg acatcacagt ga

#ttaatcca  27480

aaactatcag catcaatgaa gttaataaca atattgttca tgaaaacaaa gg

#tcatgttt  27540

atgaaattga aacattgttt atatgtgagt ggcctatttt tctcatgcta ct

#gcactaat  27600

tttatcttag ggtttataaa tatgaatcct aaatattaaa gtagtgctat tt

#atcgccaa  27660

ctctagtggc cttctgtcct cagccttttt gaattcacaa aattcctgta aa

#ctgtggac  27720

tattttcccc aacttacaaa taaagaaatt gaggttcaaa aaagtaactc gc

#caataaat  27780

aggttctaga tatctactat acagcatagt gcctatagct aaaaatactg ta

#tcgtatac  27840

ttaaaatctt ccaagagggt ggatcttatg ttgtattctt accacgcaca ta

#caaataat  27900

aataatgata gtaaaggcat tagggagctt tgggatgtga tagatatatt tc

#catgtgta  27960

agtgctgtaa gagttcacaa gggcataacc caagtgcccc agatatggcc ct

#tctgtatt  28020

gaatatacct aaggtagaca cactgaagaa gatggatata tgaaaaagtc ta

#atatacta  28080

gccttattga ggtaaattga tcagttcaca ttgggtatag aacattgtca gc

#aactagaa  28140

aaagaaaatg aggttgttcc gtctctatgt tcacacgagg catgaggcag cg

#acgttcta  28200

ataatcctcc tgctcttctc ccttaccctc ctgcctcctc aatagcctta at

#ttgtagca  28260

ttttccaata tctgtggtta aattctttcc ctatggccaa ttttatacca ct

#gaggtgtt  28320

ttcccctgaa cataaagtta ggaagagatg cgtgtaactg gcactggtga gc

#tggggtaa  28380

gccagctcta gcataccact gctgccaggt tatctaccgt agagtgtaag cc

#atagtttt  28440

catcaaaagt gtcctgcaaa aaaaaaacat tgaaaaatga gaaacagttt ct

#gtatgtca  28500

atataagtca atttttattg caatgaatat tgaaggaggt aaaatttttt tt

#tacttcct  28560

gatgaaaaca gatgaagtat gttaatatat gtccctgggc cctctgtgtt tc

#tgtgcctc  28620

ccctcacaag gcatgctatt tttctgtacc tgccaataca tatcttatct tc

#cttacagg  28680

cctctctcct ctgtttttga ctatttcagc ctactccagc ttgtagtgct gt

#agaaaagg  28740

ctttagattc atttatttat tcaagaaaca cttactgagc ttttaatatg cc

#aggtactg  28800

agaatataaa catgattaga cagaccatgc tatagctttg attgtatggc tt

#tggggcaa  28860

ttgctttttt tgttttttaa cttactgagg gatgactgac atgtaaaaag ct

#gtacatat  28920

ttaatgtata caactcaatg agtttggaat atacacccat gaaatcatta ct

#agcatcaa  28980

agccacagat atatctatca cctcccaaag cttcctaatg cctttattat ta

#ttactatt  29040

atttttatta ttattagtat gtgtgtgtgt ggtaagaaca caacataaga tt

#caacctct  29100

tggaagattt taagtataca atgcagtatt gttagctata ggcactatgc tg

#tgtagtag  29160

atctctagaa cctatttatc ggaaagttac ttttttgaac ctcaatttca tt

#atttgtaa  29220

gttggggaaa atagtccata gattgcagcg attttgtgaa gattaaatga ga

#aaatataa  29280

ataaaacact tagcatagta gatggtacat tgtagatttt ctataaaggc ta

#gtttcttt  29340

tttttaactc taaactctta tagctatctt aagtgccaaa tgaatcggca tt

#tatttata  29400

ttctgccttg gatgttgctt gccttctcta gtatcctcag cttgtacctt ta

#tgcaggtt  29460

cttatacata atttgttgtt cctatcaaca ttgatcacaa tgtagtatca at

#actttctg  29520

attcttggtt cttaatttgc ctgcccattg agatattggt cataagttaa ca

#ttttccca  29580

ttattttcca ttttgaatca ctttcctggt actttcaatt ttgtatttta ta

#tcctgtcc  29640

atctgtattt tataatttta aattttttct tccaaataaa ttttagcatt ca

#gctattgc  29700

tgtgtcacaa tccatttcca aacgcagtgg cttcaaacag caacatttta tt

#taggtcat  29760

aattctgtag gttgtgaatt tgggttggac tcagctagtt agttcttcta at

#gtgaatca  29820

gctggcgccc gcttctacaa tcagctgatg atttcacaac tgaggccggc tg

#gtttgtga  29880

agtcctcagc tggatgactg ccagctaggg cttctctctt catggtctct ga

#tctgatcc  29940

agccagctag gctgggcatg tttacatggt ggcatgactt ccagaagcaa ca

#gcaggtaa  30000

gaacctatgc ataagaaccc ttcaaacctc tgtgtcacat ttgctaatgc cc

#cattgatc  30060

cagattcaag ggttggagga atatattcca actcttgttg gaacaagctg ct

#aaaatatt  30120

gtggccattt taagagaatc taccacatta tctatgtatt tttcatttgt aa

#acatctat  30180

acagaaatgc caagtgtttt tatctttgat ttcagatatt ttaattgttt ca

#cagttgaa  30240

tttcataaac tttcctcatg gaaatctgtt tttctcctca gcaacttctc gg

#tttttcca  30300

ggcaagcctt tctgttctta attactgtaa ttttcagaat gagctacttt ct

#acatgtgc  30360

acatgtcttt taaattaata taatacaaaa ctaaatctgg aaaattttag tt

#ttacattt  30420

ttttgttcat ctcctaacct atttccctga agcaaagtga caggtctgtt ca

#gaatttat  30480

aatttaatta agatgagatt ggggaggtaa ggaagtacca ctttctcttt tg

#cattcatt  30540

ttttaaggat ctcaggacat atgttgatct attttctttc tcttccttgc aa

#attaaaac  30600

aaaatgtttt aaaataaatg ttttaaaata atagtgaaat tgcgagcttt gc

#tgattata  30660

aaaatatatg ctctatgtca tcttgccttt tcttccctgc tctaatatga ac

#ttcacatt  30720

atcccttcaa ttgctcttct gtttttgctc acgttatctc ctttttctaa at

#ttttcact  30780

cctctgctga tgtaaaacct gcttattgtt taagagcaac tcaagtccta ca

#tcctccat  30840

gaaattttca ctgattgccc aggttatcct tgattttact ctattgtgaa ct

#cctacagc  30900

atttgatggc tggtaccaca cagtaacatt tgcctcatta caggttggta tt

#gtttaatg  30960

cttttaatgt gtatttttaa tttgtattgt ttgctgctgt tttcattgct gg

#gcttgatt  31020

cgttagccag tttttttttt tactgatttg cactcctggc tctctaagtg ct

#gtaaatgt  31080

ccaggattaa gctgttttat aatataccaa aattgggagt tctcaagtca tt

#ttttttat  31140

aagaaaacac atatttttag gtttcattca cttattcaag atatattaaa tg

#cttattat  31200

gtttcaagat taaaaataaa cactatctca agacacaaag ttaatttagt tg

#ctatgttt  31260

tgctcaagac ggtgttataa acttgtaaga aacagtattt ttgaaaatgt gc

#cacagtac  31320

cttctaaact agtaaatctc agttagtggc ccttttgatg agcaacttta gg

#actttcaa  31380

gatttctact ttctatctag aatagtcata gtcatgaagc cttttgtttt at

#aatgatta  31440

taaataccct tcccagggtc aggtaactat gaccagcact agtttaacac tg

#tctttttc  31500

ttttagcaaa acaacacaag gaacaatggc acagtagcct agtaatacct ct

#ttgctata  31560

aacatacact cactcccatc ctctcagtct ctttgtttct ctgttactct cc

#cttagcag  31620

aaattttcca ttggacttct agtgctttga tgtattatga tcaatgatga ct

#tgtgtttt  31680

ctgactctgt tagagtctcc atggaattaa agattatatg cttattcagc tt

#aatgtact  31740

tgaccttttt gtatgattga cacatctaaa tttctgtagc aactcagtca tt

#atgcaaca  31800

gctgtgttat attcatttca tgtaaaaagc aaaaacaaaa gacatagagt tc

#tcttcaag  31860

agtagatacc ttgacccctt ccctcccagc taaataaaga atagtttatt aa

#taacatta  31920

ttaatcagtt tccaaatgcg tctcctttcc tcaccgcatt ttataaacat tc

#agtatact  31980

gtgaccatag tcacatcaag aatcatttca atactgatcc ttattatata at

#taaaatat  32040

tcaataattc tgagtctgtt gaacataata atagccacac aacttaagtg tc

#aaacatct  32100

aggatttgtt agcaagattt gtgctcagaa aataatatgt acaaaccttt ga

#ttttctta  32160

atgatgaaac tgtattttgt ctgaattgac atatgtgtct ttaagttaga ga

#gaaaaaac  32220

cttgacattt ttctgtgact tttccttatc aacagctgtg ttctacctgc gt

#ttattttt  32280

ctcagaattc attatgaatt ctgtataggc cttcagaagg cctatacagg ct

#ttctaaca  32340

gagattctat aggaaaaagt tttggttaac tgtttgaagt attagttgaa ga

#aggcattc  32400

tagataaggt tttacaagac agaagaaaag aatcaattca tttttagttc tg

#agcctgaa  32460

ttgtggaaac tgtactaact gcagataaac tctgaataaa ttctagtgtt ct

#ctgcttat  32520

ctcaaaaaat cttttctttt aatgatactg ttccatgctc actaatgttt tc

#aaaacata  32580

ttcatatcta aatggttttg tatttttatt aaattttgga ttttttgcat ta

#cataaagt  32640

taattttgtt gaccatttta tgaatttaag aaatgtccac ttgaaaggac tc

#gctccttt  32700

aattaaattt ttggccttta tttataaaat aaaaattatt ctttatatgt tc

#ttgaaaag  32760

taaatcagat taggattaat aattgtcaag tcattttaga acaatgacat ct

#atcattaa  32820

atttcttgaa ttttttgcct tctcaactga tagctatccg ggtgaaaaat tc

#aattatgg  32880

atattggaaa aattgatggt aatattaatc tggaaatgtt atttctgtac ta

#ttctttac  32940

aggacctgag gggattctct agttctttag gccagtgtta taatgttagg at

#ttacaaaa  33000

gttggtaata tagagagaaa caggaagaaa atgaaatggg acaggaaaat at

#cattcctt  33060

cttcttattc cttcctctaa gtcactggca ttgtgaaggg aaaagggaac ta

#acatgtat  33120

tagtgtctac catgtaacag gcattgtctt tcatatttta tatttatcgt at

#tagctcat  33180

gtaatctttg tggaaaatct cctaaatcta ttagtaggtc tttaatatct at

#gtttattt  33240

attttgtcct gaaaacaaat gaagtttttg gatcaagaca gagaattatt at

#tacttata  33300

gcaataacca ccttggaaag aaggcacaca gttatgcgca caggagggga gc

#catgaaat  33360

tatgaatctg ggaatttata taggaattac tatataaact ctttatatag ta

#aatggtct  33420

tctcctgtct tctccttttc tgaaagagga agagaaagtt tatctccgtt at

#atacaata  33480

agcaaatctt taggggagag aatgagaagg tcctggttta aaccctttga aa

#tgtaaacc  33540

agtagctctg ggattttgtt ctcttttgaa atgtaaacac agagctgtag aa

#aataagtg  33600

tctgcatatc tctgagggtc tctgtctatt cagtccacct ttaatccaga tt

#tcagtttg  33660

tcttgcttta taactcctta accatgcaga agcatgaaaa cattttctct gt

#agttccac  33720

atcatgaatt ttagcagttt tagtactgtt gctaaaaaat tgtggctatt ag

#cttgtttc  33780

cattcctttc ataaagtgtt tagtagcata atgcattatt aggtctactt tc

#tatctatt  33840

atacttgaaa accatcctct ctatgtaaaa tatctattta ttcaatggat at

#ttattgag  33900

caccaaaaac tgtcaagcat tgttctaggt atttgggata catcagtcga ca

#aatcaaag  33960

atacctgcct tgcttgtatt tacaaacttt ggggttagaa tgcataaaat tg

#agattatg  34020

gaggggttgt aattattgcc aatgaaaagc ctaggatgaa agatcactgg aa

#gactaaag  34080

tttaaggaat tgaaaggcca gaatatcaaa agaatcatct atatgtgttt tg

#aaatctta  34140

tgaattaagg cagtatcgaa gagaatgaca gtatgcaaag agctcaaatg gt

#tgagtggg  34200

aattacctgg accttagtgg ataacagcaa ccatgaggca aagtatgtag tg

#agtaatgt  34260

cgaccatgag atttaaatct gaaggatgtc aggaaggata tggggaaatg gt

#ctgaaaat  34320

gtcagaatgg agcaaagaaa taccactttg cttattccac tcacccaacc ag

#aggtcgca  34380

ggaacaagaa tgacaccttt ccatcttgca taagaactgt gggagagaag ca

#gccatcac  34440

tgagagattg taggggaggc attgtcctcc agagaaagac aggtttatgt tt

#cagctagg  34500

aaagtaaagg gaacacttag aaaattgatt tttggctcac tggaagggtt tc

#agcagttg  34560

ggagagaaca aaggtaattt ttaccagctt gtaacttcac atgtattaac tg

#tgttgcaa  34620

aactaatgaa acttactgtc tattctcttg ctttatctga taatatagat aa

#gggtgtca  34680

cctgtaatca ttgttaccat atttcttgag gccattttct tattctcatt ta

#acttttct  34740

acttgtttct tctttatttg tatttttctc tgtttttaat cttgctcttt tt

#atcatttc  34800

tgtctcttta tatcctactt acctcttaat ctttttgccc aacttctctc tt

#aatatata  34860

tatatttttg ctctttacta tttctcttat ctttctattt caaaattaca ct

#gtctgctg  34920

ttttctccaa ctccccacaa ctcaccttag gtgtagttgg gactatgcaa ta

#tgccatca  34980

cacaggtagt actaattttg acaggtagca tctctacttc aaacaaagaa ag

#ctttaacc  35040

aaaaaggaat tacaggagag aagacagtat tctccccaac tgatgctaac at

#tgccacct  35100

acacttttga cgctttcttc aacagttaag acgtagcaac ttattacttc cc

#caaattcc  35160

ctgtgctctg ttgatctgtc ttaaactcta aagggagaga aagtaggttt gt

#tcattagc  35220

tgtgggactt aaaatgtgac ttaacttttt tgaacctttt gtttcgtgaa tg

#ataaaaaa  35280

acactttctg aatgatatag ctactaatat tttcatttta tagataaagt ga

#aagataaa  35340

gtactttttt taaaggttgc ataaatataa gtgacacaca ctgatatgaa tg

#taagcatt  35400

tgactcaatc ccagagatca tgttttaatg aatactctat tgtttctcac at

#aatataac  35460

ttaatattgt ggtcaataaa ataataaata ggaccagaca catatatgta tt

#aattcact  35520

tccctttatt tcctttttcc aaaattgagc cttattggta aagggctttt tg

#tgcatttt  35580

aattgtctat aatcaggtac ttgaaccaat tataattttt cacttgcctg ca

#tgaatcca  35640

tacaggacaa aaacctgaat atagaaacta tctttcagct ttcggtttgc ca

#gaggatta  35700

atctataatt atttttagga ttataaaaga tttacatccg ttcttaaaat at

#acataata  35760

tcggattttt ttccagcaat agaggaataa ctaattctat agtttcatgc ca

#atctcacc  35820

tccagtcctt ctagaatttg gaggtaattt aaccccgtgt ataaaaaata aa

#tattttct  35880

tttttgcgtt ttattgaaaa aatcacgtaa tttaagtaca aatatatcca ct

#aaagtagg  35940

caaatttatt ttagtagaat tcagttatcc ctttcaaaga aacactatca gc

#ctaagtgt  36000

tatacattgg atattttaga aatcttacaa tttcaattac atgtcttctg aa

#actcatta  36060

ttgtaaggct ttgttttagg ctttccttgc tgtattagtt gactggggct gc

#cagaaaaa  36120

aataccacag gctgggcagc ttaaactaca gaaatgtatt ttctcacagt tc

#tggaggct  36180

gggacaccta agatcaagat ggctagccag gtgggtctca ttctgaagac tt

#ttctcttg  36240

gctttaggtg gttaccatct ccttgcatca ttgtgttacc tctttgtgtg ct

#tggacaga  36300

gagcaagaga ggtagctctt tggtgtttct tcttttaaga acactaattg ga

#tggatcca  36360

gccccactcc tatggcctca tttaacctta attacctcta taaaggccct at

#ctctaaat  36420

acagtcacat ttggggttgg gactttaaaa tataaacctc gggggacata ag

#ccttcatc  36480

cacagtattg ccattataat attttgtgta ctttggcact tgagaaagta ag

#attttttt  36540

taacctagta ttttaatgtt ttctttagag gttttttccc tgatacaaca ct

#ctcctata  36600

catgatctac ttggtaacac aaatatccct ttgtttgctt gtacttttgc tt

#cctcataa  36660

atttttctgt agctacaaat gttaactttg ttggataggc tttatttttt ag

#atcaattt  36720

taagtttata aaaatactgc acagaaagtt gagacagttc ccatgtattt cc

#tctccctg  36780

ctgcacacaa tttcttctct tattaacatt ttacattagt gcagtacatt tg

#ttacaatt  36840

gataaaccaa cattaatagg ttattatcaa ccaaagtcca tagtttacat ta

#gggttcac  36900

tctgtgttat acagttctat tggtctggac aaatgtttaa tgacatgtat ct

#accattac  36960

attatcaagg atggtttgac ttccctaaaa atgccctgtg ctccacctgt tc

#atccctat  37020

accttctccc tgaagccctg acaactgctg atatttttac tgtctctata gt

#tttagctt  37080

ttccagaatg tcatacagtt ggaataatac agtatgtagc ttttaaaacc at

#cttctttc  37140

acctagcaat atgcattaac agttctctca tgtctttttt gtggttgaca gc

#tcatttcc  37200

ttttccagta gtcccacttt atctgtagag gatacgttct aagaccccca aa

#agatgcct  37260

gaaacctcag atagtactga accctatata tactgtgttt ttcctttaca ta

#cataccta  37320

tgataaaatt taatttataa attaggcaca gtaagagatt aacagtagct aa

#taataaaa  37380

ttgaacaatt ataacaatat gccagagtcg aaactcttgt gccttgggac tt

#ttattaag  37440

tataataggt ggccaatatc aagtgtaaca tatagaaata ggaaaacaga aa

#aacctctg  37500

tggaatttgg cattaacata gaccttagcg aaacctgttt tattagagac ag

#tgattttt  37560

taaaaacact taactgtgaa gggaagggat ttgatgagat aacacaattg tc

#tgaaggta  37620

gagagaataa aaaacaattt tttttctaat gagaagagta taattaagca tg

#gggaacag  37680

acacatagag attataaagg aagtgatgat tgcaaaatat ttaaccaaat aa

#ttagtatt  37740

atacatgttt gtgatagagc tatggtacac ttaattaggt aaaatgccaa aa

#gacagtgc  37800

cacgctccaa gctttatgta tcataaacat caaaaatgac ttgctgaatt aa

#attaaatt  37860

gagtctccat taacatgtaa atcatcatat ctgtgccctg gaataattca ga

#gtttaatt  37920

tgtgggtttg cttccttatg aaggtcatcg aacactattt attggagtac at

#gtgccctt  37980

gggaggaaga aaaagccatc gacgtcacag gcatcgtggt cataaacaca ga

#aagagaga  38040

cagagaaaga gattcaggat tagaggatgg aagggagtca ccttcttttg gt

#aagaatcc  38100

ttctccttgt ttttattaag ttaattattg taatatactt gcttatacaa tt

#atgattag  38160

gagtaatacc ttatactcat aaaattgttt atacttttat aaaagacttt gg

#gccggttg  38220

gagagaagtg ggagagataa agcttgatct ttgtttttct cttatatatt tg

#cattgaga  38280

agctgagaat tgatgaagat ttatgatata ggaaatacaa ttgagtaaag ct

#caaaaact  38340

cttgataatt tatacaaata atcatcatta ctcaaagtgg tttgaaaatc ca

#gggcaaaa  38400

tgccttaatt tagttcccat ttgcactttt actgatagtg cccaagtttc ag

#tcttagga  38460

tgttgtatta gtccgttttc acactgctga taaagacata cccggactag ac

#aatttacc  38520

aaaataaaaa agaggtttaa ttggacttac agtaccacat ggctggggaa gc

#ctcacaat  38580

tatggtggaa ggcaaggaga agcaagtcat gtcttacatg ggtggcagca gg

#caaagaga  38640

gcttgtgcag gaaaactccc ccttataata actatcagat ctcatgagac tt

#actcacta  38700

tcacgagaaa agcacaggaa agacctgtcc tcattattca attaactccc ac

#tgggtccc  38760

tcccacaaca catggaaaat tcaagatgag atttgggtga ggacacagcc aa

#accatatc  38820

gttccaccct tgggccctcc caaatctcat gtcctcacat ttcaaaacca at

#cgtgcctt  38880

cccaacagtc ctccaaggtc ttaacttatt tcagctttaa ttcaaaagtc ta

#tagtccaa  38940

aatctcatct gagataaggc aagtcccttc cacctgtgag cctgtaaaat ca

#aaagcaag  39000

ctagttactt cctagataca actggggtaa aggcattagg taaatacagc ca

#ttccaaat  39060

gggagatatt ggccaaaaca aaggggctac aggcccaatg caagtccaaa at

#ccagcaag  39120

gcaatcaaat cttaaagctc cgaaatgatc tccttttact ccatgtctca ca

#tgcaggtc  39180

atgctgatgg ttctcatggt cttgggcagc tctgccctcg tggctttgca gg

#atatagcc  39240

cacctcctgg ctgctttcat gggctggcgt tgagtgtctt gttgcttttc cg

#gacacact  39300

attcaagctg tcagtggatc ttccattctg cagtcaggag gacagtggcc ct

#tttctcac  39360

agctccacta ggtggtgtcc cagtagggac tctgtggggg ctgtaacccc ac

#atttccct  39420

tctgcactgc cctagcagag gttctccatg agggccctgc ccctgaagca aa

#tttctgcc  39480

tgggcatcca ggcatttcca tacatcctct gaaatctagg cagaggttcc ta

#aaccccaa  39540

ttcttgactt ccgtacacct gcaggctcaa caccacatgg aagctgccaa gg

#cttgaggc  39600

ttgcaccctc tgaagccaca gcctgagctc tacatttgtc cctttcagct at

#ggctggag  39660

cagctgaaac acagggcacc aagtccctag gctgtacaca ggatgggtac cc

#tgtgcctg  39720

actgagaaaa ccactttttc ttcctgggcc tctgggtctg tgatgggagg gg

#ctgccata  39780

aagacctttg acatgccctg gagacatttt ccccattgtc ttggggatta ac

#atttggct  39840

cctcattact tttgtgaatt tctgcatttg gcttgaattt ctcctcagaa aa

#tggaattt  39900

tcttttctat tgcactgtca ggctgcaaat tttctgaact tttatccttt gc

#ttccttta  39960

taaaaccgaa tgtctttaac agcatccaag tcacttcttg aatgctttgc tg

#cttagaaa  40020

tttcttctgc cagataccct aaatcatctc tctcaagttc aaagtttcac ag

#atctctag  40080

ggcaggggta aaacactgcc agtctctttg ctaaaacata acaagagtca cc

#tttgctcc  40140

agttcccaac acgttcttca tctccacctg agaccacctg agattgcctg ga

#ccttattg  40200

tccatatcat tatcaagctt ttggtcaaag ccattcaaca cgtcactagg aa

#gttccaaa  40260

ctttcccaca ttttcctatc ttcttctgac ccctccaaac tgttccaact tc

#tgcctgtt  40320

acccagttcc aaagtcactt ccacattttc aggtatcttt tcagcagcac cc

#cactctac  40380

tggtatcaat ttactatatt aatatgtttt cacactgctg ataaaaacat ac

#ctgagact  40440

aggcaattta cagaagaagg aggtttaatt ggacttacag ttccacatga ct

#ggggaagc  40500

ctcacaatca tagcggaaag caaggaggag caagtcacat cttatgtgaa tg

#gcagcagg  40560

taaagagacc ttgtgcagga aaactctgcc ttataataac catcagatct ca

#tggactta  40620

ctcactatca tgagaacagc acaggaaaga cctgcccccc atgattcaat ta

#cctcccac  40680

caggtccctc ccacaacatg tgagaattca agatgagatt tgggtgggga ca

#caaccaaa  40740

ccatatcaaa tgtgaacctt ttactattgt gaatgctctc tcattgaaag ca

#tattcaga  40800

ataccacaat aagtgttttc gtagttgtta aaaggttctg aatgccatga ga

#gcccatgt  40860

acatgacata actgagaacc tggctctcag ttccttgacc atcccatctc tt

#atgacctt  40920

ctctgtcatt gcactttgtt caccttctca accatattca ctccatccct ga

#agtcacta  40980

attcatttat ctttctgtct gaccacagct tcactccttt cttgctgtgc ag

#ctacttaa  41040

cccctctact tttcttctat ccataagttt gtctttattt gtttatccta gt

#ctgattgc  41100

atagcatgca gtcttaggaa tactttagca ttactagtat tccatttgta tt

#actagtag  41160

tctatttagt aatactagta ttctaaatat cttaggttct aagttttagt tt

#tcttcata  41220

cctttactgc ctcttttatt ttcattttta ataggaagca gcattttatt ta

#aaatgttt  41280

ttaatagatt tcttaaagat gtaaataatc gaattaaact tagtctatat ta

#cttgtatg  41340

aattaattta cattttgttc acattcgtga aaaataattt agctaggtat gc

#aattccaa  41400

attgacaagt attttaactc agcactttga acataatatc tatttattta tc

#aatttcat  41460

gaagatgtta agaaaggaga taaaaatcta ttgttgctct acagttaatt tg

#gattttat  41520

atttttatga atttaaatca tttcctttat tttggtattt agttttacat tt

#attatgat  41580

attttcagac acacatatat gccttttatg cttttcttgg ttgatattta at

#gagaatgt  41640

atattattag ttctttaaaa tgcttaaaca tgtcctattt tctattattt tc

#tctcccac  41700

ttatttaaat tctttcttca aatattcatt aagcatattc ctttcaattt ca

#ttttcgat  41760

ttattttgat ccctctttta tattttttca tcattttctc cttgtcctga ca

#ttgaagtg  41820

tttattttag ctaattcatt tattcatatt ttagctcata gtttttgcct tg

#ctcatatc  41880

cctttacttt ctttaaacat tttgactaca tgtgtctttc acttctttta ct

#ttggattc  41940

gggggcatgt gtgcaggttt gttacataag tatgttgtgt gatgctgggg tt

#tgggatat  42000

ggatggtcct atcacctagg tagtgagcac agagtatagt tttacaaccc tt

#gttcccca  42060

ccctccttcc ctgctctggt gattcccagt gcctattgtt cccatcttaa tg

#tacataag  42120

tacccaatgt ttagccccac ttatgagtga gaacatgcag tatttggttt tc

#tgttcctg  42180

agttaatttt tttaggataa tgatctccag ctgcattcat gttgctgcaa aa

#ggatatga  42240

tgtcattctt tttatggcca catagtattc catgatatat atgtaccaca tt

#ttcttcat  42300

ccactttacc ataaggaaac ctagttgatt ccatgtcttt gctatggtga at

#aacactgc  42360

agtgaacata ccagtgcatg catctttttg gtggaatgat tcatttttct tt

#gagtatat  42420

acccagtaat gggattgctg ggttgaatgg tagttctgtt ttaatttctt tg

#ataaatct  42480

ccaaactgct ttccacagtg gctgaaccaa tttatattcc caccaacagt gt

#ataagcat  42540

tccgttttct ctgcagcctt gtcagcatct attatttttt gactttttaa tg

#ttcaccat  42600

tctgactggt gtgacatggt atctcattgt ggttttgact tgcatttcat tt

#gttgactg  42660

cttgtatgtt ttcttttgag aagtgtctgt tcgtgtcctt tgcccatttt ta

#gtagaatt  42720

atttgttttt tgcttgttga tttgtttaaa ttttgcttgt ggattcgggg ta

#tcagacat  42780

tttttgaatg catagtttgc aaatattttc tcccattctg taagctatct gt

#ttagacta  42840

ttgagatttg ctgtgcagag gctctttagt ttaattaggt cccacttgtc aa

#tttttgtt  42900

tttgtttcaa ttgcttttgg agacttagcc attaattctt tgtcaaagtt aa

#tgttggga  42960

agggtatttc ctaagctttc ttctagaatt attataactt aaagtcttac at

#ttaactct  43020

ttaatccaac ttgagttaat ttttgtatat ggtgaaaagt aggtatccag tt

#tcattatt  43080

ttgcatatgg cttgacagtt atcccagcac catttattta atagggagtc ct

#ttctgtat  43140

tagttattct tggtgacttt gttgaagagc agactgttgt aggtgtttga ct

#ttatttct  43200

ggattctcta ttctattcca ttagtgtgtg tgtctgtttt ttgtaccagt ac

#aatgctgt  43260

ttgggttaat gtagccatag agtacagttt gaagtcaggt aatatgatgc ct

#ctgacttt  43320

gttctttttg cttagaattg ctttggctat ttgggctctt ttttgattcc at

#attaattt  43380

tagaatagtt tttctaattc tgtgaaaaac aacattggtg ttttgataga ga

#tcggtatt  43440

gaattctgta aattgctttg ggcagtatgg ccattttaat gatattgatt ct

#tcctattc  43500

atgagtgtgg aacattttta catttgtttg tgttgtctct gatttctttc ag

#cagtgttt  43560

tgtagttctc cttgtagaaa tctttcacct ctttggttag atgtattaca tt

#tttttgtg  43620

tgcctattgt aaatgggatt gagtttttga cttggctctc tgatacaatg tt

#attgctgt  43680

acagaaatac tattgacttt tgtacattga ttttgtctcc tgaaactcta ct

#gaaattgt  43740

caattctagt tgccttttgg tggagtcttt agggttttct atttctaaaa tt

#ataatcat  43800

cagcaaagga gagatagttt gacttcctct cttcctattt gaatgccttt ta

#tttctttc  43860

tcttgcctga ttgctctggc taggtcttcc ttatactatg ttaaatagga gt

#ggtaagag  43920

taggcatcac tttcttgttc tggttctcca ggggaatagt tatagctttt gc

#ccattcag  43980

tatgatttta gctgtgtgtt tttcatagat ggctcttatt gttttgaggt at

#gtttcttc  44040

aatgactagc ctgttgaggg tattttatca tgaagggatt tgggattctc tt

#gaaggcct  44100

tttctgtatc tatcgagata accatatggt tttgattttg attctgttta tg

#cgatgaat  44160

catatctagt gaattgtgta tgtcgaacca accttgcatt ccaggaatga ag

#cccacttt  44220

tctcatagtg aattagattt tgatgtgctg ctgaattcag tttgctagta tt

#ttgttgag  44280

gattttgtgt ctatgttcat cagggagttt agcctgaagt tttctgtttt tg

#tgtctctg  44340

ccagattttg gtataaggat gatgatgact ttgtataata tgttagtgag aa

#gcctcccc  44400

tcatcctcaa ttttttggaa gagttttagt aggattggta ccagttcttc tt

#tgtaactc  44460

tagtagaatt cagctgtgaa tccgcctggt tcagggcttt ttttggttgg ta

#ggtttttt  44520

taaaattacc gattcaattt cagaacttgt tattggctta ttcatgtttt ca

#cattatcc  44580

cttgttcaac cttggatggt tttgtgtttc tgagaactta tccatttcct ct

#agattttc  44640

taatttgttt gcacagaggt gttcataata gtctctgaat atcttttgta tt

#tctgtggg  44700

attgggtgta atgtcatttg tcatttttga ttgtgcttat ttgggtcttc tc

#tttttttg  44760

ttaatctaac tagtagtcta tcaatcttat ttattctttc aaaaaacaaa ct

#ctgtttca  44820

tttatctttg tatggacttt tgcatctcaa tttctttcag ttgttctctg at

#tttagtaa  44880

tctcttttct tctgctagct tttaaagcca tacttatgtt ggggttcctc ca

#tttttcca  44940

ttttctcctt gcctccacaa gcagatatac tctgctggaa atcatcattc aa

#caaggcag  45000

attgtaacca ttatgaagtt atgactcaag gagaccttca acatctcctc ct

#aatttcat  45060

tgtgtatctt ttttgacatt tgaaataatt atttttcaac tttcttcgcc tt

#cttcatca  45120

ttctccaaca tcctctcttt tcaccattac ttgatagtaa tcttgctttg ta

#cttcagag  45180

ggaaaatata tcatcagaaa gaactcactt tactttcttc ctgttaaaaa gt

#tatagctg  45240

aaacctttct tcctattaaa cggttaaaac tgcaagaaaa taaggaagtt tt

#cttttcct  45300

ttatgtttat tttctattcc ctctcaccac tctggaaact tatgccattt ct

#aatttaat  45360

tgacctcttc ctcttgaaat gaatttttct tatcatcttt gaaacatgat ag

#agtctcca  45420

ccattttaag cagttctcca acctcctgca aacccacctt tagtcattca ga

#tatgtaag  45480

ttaactgcat ataaatgttc tgggtagcaa ttttactttt aaatatctct cc

#atattgct  45540

ttatttggtt tattcaatat ctggcttcag taactattgc agataagtct at

#agtctctc  45600

tatttttatt ttttaggttt atgtatttta atcctgaatg tttatagaca tt

#tttctgtg  45660

tcccttaatg aagaaaattg ctaagattga cctaatggta ggtgtattaa aa

#aacttttc  45720

catcccgcat acacgaatag ttttccacct agggaacatt ttcctattat gt

#ttcattct  45780

gttccattta ctttgatctc tttgtgaaga ctttctttgc tcatatccct ct

#actttctt  45840

caaacatttt aactacatat atctttcatt tttttttaac tttgaatttg gg

#ggtacatg  45900

tgcaggtttg ttacatgagt atgttgtatg atgctgaggt ttggggtaca ga

#tggtccta  45960

tcacgcaggt agtgagcaca gagtatagtc aattttacaa cccttgttcc ct

#accctcct  46020

tcccagctcc ggtgattcca agtgcctatt gttcccatct ttatgtccat ga

#gtacccaa  46080

tgtttatctc ccatttatga gtaacaacat gcagtatttg gttttctgtt cc

#tgagttaa  46140

tttgcttaga gtaatggcct ccagctgcat tcatgttact gcaaaaggat at

#gatgtcat  46200

tctttttatg gctgcacagt attccatggt gtatatgtac cacattttct tt

#atccacct  46260

caccctaatg gtacctagtt gattccatgt ctttgctatg gtgaatagca ct

#aagatgaa  46320

catgcacgta tatgtcagat ttctgatttc tgctctgtat ccttttcctc tg

#tagtttaa  46380

tgttagtctt ttatattacc atttgattat ctgcagaata aattctgcat tt

#tcctactt  46440

ttattatgag ttttggtttt gctgttgcat ttttagtttt cattaatttc tt

#tcttattt  46500

catcctattt tctttacatt ttagcctgtc ctttcctgaa tactttttat tt

#ttttctgg  46560

ttggtagagt gtatccccag tgatttctgg acgttttcat tttatcctaa ag

#tagacaat  46620

tttcagagct atgcttttcc tttggactgt cagattattt ttactctcca tt

#gattttta  46680

gtatttttta tggactccta ggttttttcc tttttttctc atttttaaac aa

#ggaaaggt  46740

agattcctac tatatctacc tagctatatc ttaagattgc ttaatgaggc tg

#ctgtcagt  46800

atgctccatg tttccaacag tatgtataat aagcatcaca cttatccaaa tg

#ccctgtac  46860

ttctgccagg ggcagcatag ttgttggtgg cagagtatgt aaagaaaagt ac

#tctaggta  46920

tcctgcacca ccatgataaa gaaggatggt tgtccataag aatgggcaga tg

#ggctgaga  46980

gtgtaggata tactaagtat cttctgcatt ttcagatgtt gtctctttca tg

#aaggaacg  47040

tcttagagtg taaaaaaatg acaatttggc atatttttct cattcaagtt cc

#atctgctt  47100

atagttagca gagatgccct cttagactgc aggaatggat tatctgtagg gc

#tatgcgct  47160

aatgatgagt tttcatcatt ttctagtatt tgagaaaata tatttatatc at

#cttacaag  47220

tatttcatga gcaaataaaa ataagctgta tttatcattt gtttgttccc tg

#tgcctctt  47280

ctttattttt ccctaactgg aggcattatg ccagtttttc tagaacagtg gt

#tctcaata  47340

atgactgcat ttgagaattc taaaaccgtg ctaatgctca acccgtacac ca

#accagaat  47400

ctctgtgcct ggggcctaag catgagtatt ttttgaaaag tacccccagg tg

#attcttct  47460

gtggagctgt tgatagctcc acagaaggtt gatatccact gttctggaaa ct

#ttgctatt  47520

taaatttagt tcatcagggg tctaatatcc agaatctata aggaacttaa ac

#aactcaac  47580

aagcaaaaat caacgtgatt aaaaagtggg taaagacatg aacagacact tc

#ttaaaaga  47640

agacatataa gcagccaata aacatatgaa gaaatgctca atatcacgaa tc

#atcagaga  47700

aatgcaaacc aaaaccacaa tgagatacta tctcacacca gtcaaaatgg tg

#attatcaa  47760

aaagttaaaa aataacagat tctgacaaag ctgcagagaa aagggtatgc tt

#acacactg  47820

ttggtgggaa tataaattgg ttcagccact gtggaaagca gtttggagat tt

#ctcgaaga  47880

acttaaaaca gaacaactat tgacccagca atgtcattac tgggcatata cc

#caaaggca  47940

aatgaatcat tctatcaaaa ggcacatgga cacgactgtt aatcacagtg ct

#attcacca  48000

tggcaaagac atggaatcaa cctaggtgct catcaacagt ggattgaata aa

#gaaaatat  48060

actccatggc atacattgca gccctaaaaa agagcaaaat catgttcttt gc

#agcaacat  48120

gtatacaact ggaggtcatt atcctaagtg aattaatgca ggaacagaaa ac

#caaatacc  48180

acatgttctc acttataagt gggagctaaa cattgggtag ttgtgaacat aa

#cgatggca  48240

acaatagaca ctggaaacca ccagagagga gagggagggt ggggaactag gg

#ttaaaaaa  48300

gtaactattg ggtactatac tgcccactac ttgggggaca ggatcagtca ta

#ccccaaac  48360

ctcagcatca ttcaatatgc ccatataaca agcctgcaca tgtactccct ga

#atctaaaa  48420

taaaagtaga aattattttt aaaacttacc aaacgtaaag aaagaaacct gt

#actgctag  48480

cttttaaaag ttatttaata aataaaccta ttttataaca aaaatagtaa aa

#ataaattt  48540

ctacttcaaa gtataaagcc aacaatatta gcattaaatt taaacttgcc ag

#aaatgcag  48600

aatctcaggc cccatccaga cctcttgagt caggacctgt acattaaaaa ta

#tatttagg  48660

taactggtat ggtttggctc tgtgtcccca ccaaaatctc atctccattt at

#aatcccca  48720

tgtgttgagg gagggacctg taatccccat gtgtccaagg agggaggtga tt

#ggattttg  48780

ggggcggttt ccctcatgct gttctcgtga tggtgagtga tttctcatga ga

#tctgaagg  48840

atttataagg cagtgttccc agctctttgc tcgctcgctc ttctgccgcc tt

#gtgaagaa  48900

agtgcctact tctccttccg ccatgattgt aagtttcctg aggcctctcc ag

#gcatatgg  48960

agctgtgaga caattaaact tctttccttt ataaattacc cagcctcagg ga

#agctcttt  49020

atcacagtgg tgaaacagac taataacagt aacgtatatg aatcttaaaa tt

#tgacgcca  49080

agcgatgctc tagaacattg cttatcaaac ccttctggca cattgggaat ca

#cttgagaa  49140

gctttaaaaa aattattgat gctaggcttc aacctcgaag gatttttatt ta

#attaatct  49200

tgggtgtttc cctaggcact ggtattttta aaaagtaccc caaattattt aa

#taaccact  49260

taaataattg accaagaatc agattctgag aagcttctgc ctctcaattt gg

#tgaaactt  49320

ggaaataagt cgggtggccc agattctccc tcttattttt tgccactatt tt

#tggatgcc  49380

acctaccttt ttccttcttc aatcatctga gtatcttcag tgacatttag ac

#ctaaatgt  49440

ggtttatcag tgacaaatgt ttggcacttg gtggtttcta agcaatggaa tt

#ttctagat  49500

ttcacttttt tcagtttctc tagtactaat cttctgcctt catccttatt cc

#acactcag  49560

tttatttgct ataataagta ctcagtcaca cacagagact tcaaccaaac cc

#taaacacc  49620

atcctatctg atttgggttt tgatattctg catagtgaga atatatgaca tt

#tccatgct  49680

gaaggcatta aagaaaattt ctgcctactt aagaaatagt tattttacgt gg

#aagcattc  49740

caaagaaaat attttgaaga tatttctgca ggtgcctcaa aattctttgg aa

#ttcaactt  49800

ccgaagaagt ataggataga ggagaattta agagagtatc aggtctctct gc

#tatgaagc  49860

tagatatatg ttgttaattg cagtatgaat ctgtgaaatc atggaatcat ta

#gggcccaa  49920

attatgaagc aagcatcaat ttaacaaaac gatttttgga aaaacgtttg aa

#tttgggca  49980

ctcttttttt tattattata ctttaagttt tagggtacat gtggacaacg tg

#caggtttc  50040

ttacatacgt atacatgtgc catgtgtggt gtgctgcacc cattaactcg tc

#atttagca  50100

ttaggtatat ctcccaatgc tatccttccc cccctccccc caccccacaa ca

#gtccccag  50160

tgtgtgatgt tccccttccc tgtgtccatg tgttctcatt gttcaattcc ca

#cctgtgag  50220

tgacaacatg cggtgtttgg ttttttgtcc ttgcaatagt ttgctgagaa tg

#atggtttc  50280

cagcttcatc catgtcccta caaaggacat gaactcatca ttttttatgg ct

#gcatagta  50340

ttccatggtg tatatgtgcc acattttctt aatccagtct atcattgttg ga

#catttggg  50400

ttggttccaa gtctttgcta ttctgaatag tgccgcaata aacatacatg tg

#catgtgtc  50460

tttatggcag catgatttat agtcctttgg gtatataccc agtaatggga tt

#gttgggtc  50520

aaatggtatt tctagttcta gatccctgag gaatcgccac actgactttc ac

#aatgattg  50580

aactagttta cagtcccacc aacagtgtaa aagtgttcct atttctccac at

#cctctcca  50640

gcacctgttg tttcctgact ttttaatgat tgccattcta agtggtatga ga

#tggtatct  50700

cattgtggtt ttgatttgca tttctctgat ggccagtgat gatgagcatt tt

#ttcatgtg  50760

cctgttggct gcataaatgt cttcttttga gaagtgtctg ttcatatcct tt

#gcccactt  50820

tttgatggga ctgtttgttt ttttcttgta aatttgttta agttcattgt ag

#attctgga  50880

tattagccct ttgtcagatg agtaggttgc gaaaattttc tcccattttg ta

#ggttgcct  50940

gttcactctg atggtagttt cttttgctgt gcagaagctc tttagtttaa tt

#agatccca  51000

tttgtcaatt ttggcttttt gttgccattg cttttggtgt tttagacatg aa

#gtccttgc  51060

ccatgcctat gtcctgaatg gtattgccta ggttttcttc tagggttttt at

#ggttttag  51120

gtctaacatt taagtcttta atccatcttg aattaatttt tgtataaggt gt

#aaggaagg  51180

gatccagttt cagctttcta catatggcta gccagttttc ccagcaccat tt

#attaaata  51240

gggaatcctt tccccattgc ttgtttttct caggtttgtc aaagatcaga ta

#gttgtaga  51300

tatgcagtgt tatttctgag ggctctgttc tgttccattg atctatatct ct

#gttttggt  51360

accagtacca tgctgttttg gttactgtag ccttgtagta tagtttgaag tc

#aggtagcg  51420

tgatgcctcc agctttgttc ttttggctta ggattgactt ggtgatgtgg gt

#tctttttt  51480

ggttccatat gaactttaaa gtagtttttt tccaattctg tgaagaaagt ca

#ttggtagc  51540

ttgatgggga tggcattgaa tctataaatt accttgtatc tcccactgtt at

#tgtgtggg  51600

agtctaagtc tcttcatagg tctccaagaa tgtgttttat gaatctgggt gc

#tcctgtat  51660

tgggagcata tataattagg acagttagct cctcttgttg aattgaaccc tt

#taccatta  51720

tataatgccc ttctttgtct ttttcgatct ttgttgggtt aaagtctctt tt

#gtcagaaa  51780

ctaggatttc aactcctgct tttttctgct ttccatttgc ttggaaaatt tt

#ctccctcc  51840

ctttatttga gcctatctgt atcttggcat gtgagatgga tttcttgaat ac

#agcacgcc  51900

aatgagtctt gactcttttt ttttttcttt tttttcttga tgcagagtct tg

#ctctgtca  51960

cccaggctgg agtacagtgg catgatcttg gtcactgcaa cctctgcccc ca

#ggttcaag  52020

taattctcct gcctcagcct cccaagtagc tgggattaca ggcatgtgac ac

#cacgccca  52080

gctaattttt gtagttttag cagagatggg gtttcaccat gttgatcagg ct

#ggtcttga  52140

actcctgtcc tcaggtgatc cacccacctc ggcctcccca aaagtgcttg ga

#ttacaggc  52200

atgagccagg gccttgactc tttatccagc ttaccattct gtgtcttttg at

#ttgggcat  52260

ttagcccatt taattgaaga ataatatctt tatgtgtgaa tttgatcctg tc

#atcatgat  52320

gctagctagt tattttgtag atttgttagt gtagttgctt catagagtca tt

#ggtctgtg  52380

tacttcagtg tgtttttgta gtggctgcta atgattttcc ctttcatatt ta

#gtgctttt  52440

ctcaggagct cttacaaggc aggcaggcca ggtggtgaca aattccctca gt

#atttgcgt  52500

gtctgaaaag ggttctattt ctccttcact tatgaagcgt ggtttagcca ga

#tatgaaat  52560

tttgggttag aaattctttt ctttaagact gttgaatatt ggcccccagt ct

#ctgctggc  52620

ttatagggtt tccactgaga tgtttgctgt tagtctgatg gacttccctt tg

#taggtgac  52680

ctggcttttc tctctgcgct gcccttaaca ttttttcctt catttctacc tg

#gagaatct  52740

gatgactata nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nn

#nnnnnnnn  52800

ctaaattatt acattcaatg aaatgtaata attgacaaaa ttttatttta tt

#ttattatt  52860

attatacttc tagggcacat gtgcacagca tgcgggtttg ttacttatgt at

#acatgtgc  52920

catgttggtg tgctgcaccc attaactggt catttacatt aggtatatct cc

#taatgcta  52980

tccctccccc ctacccccac cccatgacag gccccagtgt gtgatgttcc cc

#ttcctgtg  53040

tccaagtgtt ctcacattgt tcagttccca cctatgagtg agaacatgtg gt

#gtttggtt  53100

ttttgtcctt gcgatagttt gctgagaatg atggtttcca gcttcatcca tg

#tccctaca  53160

aaggatatga actcatcctt tttatggctg catagtattc catggtatat at

#gtgccaca  53220

ttttcttaat ccagtgtatc attgatggac atttgggttg gttccaagtc tt

#tttttttt  53280

ttcattgtta ttttttccag actttttttt ttttattata ggttccaagt ct

#ttgctatt  53340

gtgaatagtg ccgcaataaa catatgtgtg catgtgtctt catagcagca tg

#atttataa  53400

tcctttgggt atatacccag taatgggatt gctgggtcaa acggtatttc ta

#gttctaga  53460

tccctgagga atcgccacac tgactttcac aatgattgaa ctagtttaca gt

#cccaccaa  53520

cagtgtaaaa gtgttcctat ttctccacat cctctccagc acctgttgtt tc

#ctgacttt  53580

ttaatgattg ccattctaag tggtatgaga tggtatctca ttgtggtttt ga

#tttgcatt  53640

tctctgatgg ccagtgatga tgagcatttt ttcatgtgcc tgttggctgc at

#aaatgtct  53700

tcttttgaga agtgtctgtt catatccttt gcccactttt tgatgggact gt

#ttgttttt  53760

ttcttgtaaa tttgtttaag ttcattgtag attctggcta tcagctcttt gt

#cagatgag  53820

taggttgcga aaattttctc ccattttgta ggttgcctgt tcactttgat gg

#tgatttct  53880

tttgctgtgc agaagctctt tagtttaatt agatcccatt tgtcaatttt gg

#cttttgtt  53940

gccattgctt ttggtgtttt agacatgaag tccttgccca tgcctatgtc ct

#gaatggta  54000

ttgcctaggt tttcttctag ggtttttatg gttttagtct aacatgtaag tc

#tttaatcc  54060

atcttgaatt aatttttgta tatggtgtaa ggaagggatc cagtttcagc tt

#tctaccta  54120

tggctagcca gttttcccag caccatttat taaataggga attctttccc ca

#ttgcttgt  54180

ttttgtcagg tttgtcaaag atcagatagt tgtagatatg cggcattatt tc

#tgagggct  54240

ctgttctgtt ccattgatct atatctctgt tttggtacca gtaccatgct gt

#tttggtta  54300

ctgtagcctt gtagtatagt ttgaagtcag gtagcgtgat gcctccagct tt

#gttctttt  54360

ggcttaggat tgacttggtg atgtgggttc ttttttggtt ccatatgaac tt

#taaagcag  54420

ttttttccaa ttctgtgaag aaagtcattg gtagcttgat ggggatggta tt

#gaatctat  54480

aaattacctt gggcaatatg gccattttca tgatattgat tcttcctacc ca

#tgagcatg  54540

gaatgttctt ccatttgttt gtatcctctt ttatttcatt gagcagtggt tt

#gtagttct  54600

ccttggacga ggtccttcgc atccctttta agttggagtt ctaggtattt ta

#ttctcttt  54660

gaagcaattg tgaatgggag ttcattcatg atttggctct ctgtttgtct gt

#tattggtg  54720

tataagaatg cttatgattt ttccacattg atttttgtat cctgagactt gt

#tgtagttg  54780

cttatcagct taaggagatt ttgggctgag atgatggggt tttctagtat at

#acaatcat  54840

gtcatctgca aacaggggac aatgtgactt cttttcctaa ttgaatgccc tt

#tatttcct  54900

tctcctgcct gattgctctg gccagaactt ccaacactat gttgaatagg ag

#tggtgaga  54960

gagggcatcc ctgtcttgtg ccagttttca aagggaatgc ttccagtttt tg

#tccattca  55020

gtatgatatt ggctgtgggt ttgtcataga tagctcttat tattttgaga ta

#catcccat  55080

caatacctaa tttattgaga gtttttagca tgaaaggttg ttgaattttg tc

#aaaggcct  55140

tttctgcatc tgttgaaata atcatgtggt ttttgtcttt ggttctgttt at

#atactgga  55200

ttacatttat cgatttgcat atgttgaacc agccttgcat cccagggatg aa

#ggccactt  55260

gatcatggtg gataagtttt tgatgtgttg ctgtattcag tttgccagta tt

#ttattgag  55320

gatttttgca tcaatattca tcaaggatat tggtctaaaa ttctcttttt tt

#gttgtgtc  55380

tctgccaggg tttggtatca ggatgatgct ggcctcataa aatgagttag gg

#aggattcc  55440

ttctttttct atcgattgga atttgggcac tcttaaaaag ttttattact cc

#aacgtata  55500

agcaacatca gcagaatcct actttattat gagacccaat catagaatac ag

#tgttgtta  55560

aaacatccta gttgcattag tgttgcattc aggtaaaaga ataggccttt aa

#tatagacg  55620

gaagagttta tgcttacatc ataggaaaac aatgactggt tcaagcctac ca

#tatgtcat  55680

ggttgggctg tgattcctag gtgagtctaa agaggaactg gcttttggtc tg

#tgtggtag  55740

tggtggtggt gatgttttgc tcatacaaaa aacttttaat gcccacaaat aa

#gttcaacc  55800

tactttggct actgtactta ataaatataa taaatatatt aatttgttta ga

#tgaatgtg  55860

atgatgatta attaattctc cttcctattg caatcaactc cccagtaaca aa

#gctgctaa  55920

aatttcactt tttttttttg agacagagtc tcactctgtt ggccaggctg ca

#gtgctgta  55980

gcacagtctt ggctcactgc aacctctgcc tccctggttc aagcgattct cc

#tgcctcag  56040

cctcctgagt agctgggatt acaggcacct gccaccacag ccagctaatt tt

#ttgtattt  56100

ttagtagaga cggggtttca ccatgttggc caagctggtc tcgaactcct ga

#cctcgtga  56160

tccacccgca ccagcctccc aaagtgctgg gattacagga atgagccacc gc

#atccagcc  56220

cacatttgtt atttttaatg tcatcttcta ttctctttgt ataatttgaa ac

#tatatttt  56280

caactgggaa catggatgag ctgctttaaa ttggtaagtt tgaagcataa gc

#ttgaagtc  56340

agtgaaaata tgaaagatga tgagggaaat ttgtaacact tcaacgttta tt

#tttttcct  56400

caacctccct gaaaagaatc taatagaaaa gatgatagga ttatgccaat ta

#caattagc  56460

taatgtataa gaagtagaaa taaatctaaa agatacagac tattaaacac at

#gtttaaaa  56520

tatggtacac aaagatactg aataaattaa cacagtcctg gaattataat ag

#gattttgt  56580

cagtcttagg tggtaaattg tgcacactct ttaggagaaa tgaagcaaat at

#agaaaaca  56640

tgacctcaaa gagcaatttt ttgatggaca gtggcttcct gttcctattt ta

#atgaccaa  56700

ttaggtgcta tatgagaata tcaaggtgtt tttacaaatg tattttattg ta

#aagtataa  56760

gacaagcatt cacaagtgtt aaagcataga aacatacata taaaacccaa tg

#aattatca  56820

caccagaaca tctgtgtaat accaccttgg ctggcactct agaaactcac tt

#tgtgctca  56880

ttaccagtca ttaggttttc catcctcctc aaaagaatct ctggcctttc tt

#tttacaat  56940

gggtattttg cttgtttttg aacgttatat aaatgaaatc atataagagg aa

#ttaattgc  57000

tcagtgttct gtttatggaa ttcaccaatg tttttgatgt agcttcagcc ta

#ttcatttt  57060

cattattgta tagtatgtta atgtgcttct atatgcacgg tatgtatgca tt

#ctactatt  57120

gatggtcatt tggatcatat gcaattagaa gctactacaa gtaataatgc tg

#tgaacatt  57180

tttctatatg tcttttggta tacatatgca tttctcatac cgatgaatga aa

#ttatcaat  57240

tgctgagtca taggacatgc atattttcag ttttggtaga taatgccaaa ta

#gatttcca  57300

aaattggggt acatatttac attcccacca ataaagtgtg agaacttatg tt

#tttttgca  57360

tccttactaa cacttggtaa ttccattctt ttaacattag ccattctctt aa

#ggtatgta  57420

attatatctt attgttttaa tttatatttc ttgattacca atgaaattga gt

#aactttgc  57480

atatgccttt ggccatttgg atattctctt ctaggaagtg cctaccaaag tc

#atattttt  57540

aatgagcttt tattgatttg tagaagttct ttacatgtta tggaaataag tc

#ctttgtta  57600

gttttatgtg ttttaaatat cttctcacta ttgtgggttc tgatttcact ct

#cataatgg  57660

tatttttttg atgtggctac agattccagc agagtctgct aagaggctga ta

#cctttatt  57720

ctttaggcaa atttttctat gttatttatt tccattatat gttttagtat at

#atagaagc  57780

agacccatat cttgatcttc cataatcttg gctgaagttt gtatttcact gc

#tctatggt  57840

ttcagtggct atcataaaaa taaacatcca tcaacacagg agaaatattc ta

#ttaactta  57900

gacaattctg ccaggtgctg tagctcacac ctataaaccc agttacttag aa

#ggctgagg  57960

tgagagaatt gcttgagccc aggagttcag ggttacagtg atcatgccat tg

#cactccag  58020

actgtgtgac agaacaagac agcatctcta ataaaaataa caatttttaa ca

#ggaagatt  58080

ttttctgatt ttgatagtac tgcaatttac atgaaatatg taatactatt tt

#aaggtgtc  58140

tatttttaat agacatgaaa aatgggtgtt gaattacaca tttggaaaat tt

#actgtatt  58200

gaaacataat cttaatccct ttttaagatc ttaaaaatat gttagtagga tg

#gttatgaa  58260

aaatcttttg tgaaaataac ctaataccta taaaatcatt tctattttaa ag

#aatgaagg  58320

cctgatacag ggaaccatac gttatcttga atcaaaataa aatatttctt gt

#cgctgaat  58380

agatgaccct atttcaataa attattattt tctttaccat tgctgctatc at

#tgtgtttt  58440

agggaagcct tttgaatacc tgacacccta tctcacactt tcaaatactc ct

#tattcata  58500

actgtgaggg tgttataacc acatgtttac ttacaaatag tattttaaag gt

#gtgtagtg  58560

agtaagcctc atgctttata aaaggaaaca ctaataagcc ttaaaattaa ca

#ctcatgta  58620

catagcaatt gagatttggg ggttggatgc atggtattat agacatccag at

#tactgatg  58680

aagagtgaac tgaaataagt ctttggaaac agtgatgaga gaaaatgttt ca

#gagacatg  58740

gggaccctaa taccaatgtg gaagcatggc tgctatgaga tgtgacctct ga

#gaagtgat  58800

tgggtagtca gaactggttg tcatgcaaca caaaatgact atgtctgctc ac

#actgggtc  58860

agtctaatgg gaatatttaa ttgatttctt agtgtaactc tagaatcaca aa

#ttgtgctt  58920

ttttttaaat ggctattcaa agtactgata ttttttctag accaactagt ct

#gagagata  58980

acaggctaat taaaaatgca gttgaccctt gaacaatatg ggtttgaact gt

#gcaggtcc  59040

acttacacat agacttttac atttatatgt atattatgta gtttttgtat at

#tatgtatt  59100

tttatattaa aaatgtatgg gccaggcgca gtggctcatg cctgtaatcc ca

#gccttttg  59160

ggaggcctag aaacacagat cacttgaggc caggagttgg agaccatcat gg

#ccaacatg  59220

gcaaaacctc ctctctgcta aaaatacaaa aattagctag acatggtgat gc

#gcacctgt  59280

agtcccagct atttgggagc ctggagcagg agaactgctt gaacccaaga gg

#tggaggct  59340

gcagtgagcc aagacagtgc cactgcactc cagcctggat ggcagaaaga aa

#ctgtctca  59400

aaaaaaatta tgtgtatata tatatacttt ttttttagat ttgtgacatt tt

#gaaaaaac  59460

tcacagataa actgcatagc ctagaaatat aaaaaaatta ggaaaaaagt at

#gtcatgaa  59520

tgcataacat ataggtagat actagtctat tgtatcacat actaccataa aa

#tctacaca  59580

aatctattat aaaagttgaa atttatcagg ccttatgtac acaaacactt at

#agattgtg  59640

catggtgtca ttggcaactg agagaaatgt aaacaagtgc aaaaaatgca gt

#attaaatc  59700

ataactgcat acagtttact gttgtactta atgtactact gtaataatgt tg

#tagccact  59760

tgctgttgct attgtgtgag tgcaagtgtt tccagtatcc acttaaaaca cc

#ttgtgatg  59820

ctaatcacgt ctacctgagc agttcatctc ttcagtaaac agcatattgc cg

#taaaaaga  59880

atgatctctc atggttctca catatttttc atcatgttta gtataatatt gt

#gaaccttg  59940

aatataacca cggaacccgt atgaagtgcc acagtgatgc tcgaagtgct cc

#caagaagc  60000

agagaaaagt cataacatta caagacaaag ttgaattgct tgacatgtac tg

#cagattga  60060

ggtttgcagc agtggttgcc caccgtttca ggcagataac ataaaaagat gc

#agaaactt  60120

atcaacaaat acagtaaagt actgtaagtg tattttcttt catttatgat tt

#ttgtaaga  60180

gaaaggatat ctgcttgaac aggtttttaa agcagacgaa agtgcccaat tc

#tgggggga  60240

aaatgccaca aaggaagaga acatcagtat ttaaagcaga aaggaatagg ct

#aactactg  60300

ttttttggca attgccgcta ggtttatgat caagactacc cttatctata aa

#actactaa  60360

ccctagatcc ttgaaaggaa aagatgagta ctgcctgcca gtctcttggt tg

#tactaaaa  60420

ggcctggaca atgagaatcc tttttctact ttggttctat cgatgctttg tc

#cctgaagt  60480

caggaagtac cttaccggta aggaaatgcc tttgaaaatc ctttcaatgt tg

#gacaatgc  60540

ctctggccgt gtagaaaccc aggagctaat gttcatgaag gtgttaaagt ga

#tctacttg  60600

ccccaaaaca caaaacttat aatcagcttc tagatcaggt tttgtaagga cc

#tttaaggt  60660

tcattacaca tggtacccta tggaaagcat cgtcaataat gtggaagaga ac

#cccaatag  60720

agaagacatc atgaaactct agatggatta caccattaaa gatgccttca tt

#gctacaga  60780

aaaatccatg aaagccatca agcttgaaac cacaaattcc tgctggagaa aa

#ctgtgttc  60840

cagtgtgcat gacatcacaa gatttacaac acagccaatc aaggaaatta tg

#aaacagat  60900

tgtgaatatg gcgaaaaagg tgggggtaaa aggtatcagg atatggatct tg

#gagaaact  60960

caacagcaaa cagaaaccat gtcagaggaa ttaatagaag atgactcgat ga

#agatgagt  61020

atttctaaac cagcgccaga agataaggaa gaaaacattg aaaaagcagt gc

#cagaaaac  61080

aaattcacat tagacaatct ggcagaagag ttacaattat tcaagactag gt

#tcaacttt  61140

ttttacaaca tggacccttc tataatatgt gcactgaaac taaaataaat gg

#tggaagaa  61200

ggatcgcatc tcatggaaac agttttagag aaatgaaaaa gcgaaaaggt ca

#gaaattac  61260

aatttatttc cataaagtta catcaagtgt gtctgcctct cttgcctccc ct

#tctacctt  61320

ttctgcctct gccactcctg agatagcaag accaacccct cctcttcctc ct

#cctcagca  61380

tactcaacat gaagacaatg aggatcaagt cctttatata atccattttc ac

#ttaatgag  61440

tagtaaatat attttctctt ctttgtgatt ttcttgtttt ctccagttta tt

#gtaaaaat  61500

acagtacata atacacataa tatacacatt atgtgttaat tgactatgtt at

#cattaagg  61560

cacctggtca acagtaggct attagtagtt aagttttgag ggagtcaaaa gt

#tatataca  61620

gattttcagc tgtgtgggag atcagcacct ttaagacctg tgttattcaa ga

#gtcaactg  61680

tagttgcttt tttttctttt ctaccttgaa catcttcctg cagatgctcc at

#catcttcc  61740

tagctctagt ttcttatctc taatggaggt aaagcaggaa agttcttact tc

#actgctac  61800

tgtggcaagt taatgtcaca ctccttaggc ttagcaagaa tttgagttta tt

#cattctct  61860

cctggaggtt ttctcacctg cactcttttc tgcgttacta tttattcctc tt

#catcccct  61920

aggcattcag ttataatgat agagtctctc tgctgaaata ttctcagtgc tc

#tgtggcag  61980

cccaagatga ctctatattc cacaccctct ctctctcttc tccccgctcc cc

#tctcatgt  62040

gtgtggctta tgtatgattc acagaagaca cacacacact cagattgagt gc

#tctggtaa  62100

atactgaaag tgtgtgttat tgaatgcagc aatgtcagcc atcagcagct ag

#gctgactt  62160

tatgtttctc aggtaagaat cataccccta ctgccatccc ttttaaggag aa

#taagtaaa  62220

tgtcagactc atgttacagc tctttccgaa gaactctaaa atgtgtctgt tt

#catctcat  62280

gatcctttat agccagcctc tgtgtgggtg aaaaattaga gtcacataac ta

#ggttttta  62340

gagcatggtt tgcaaattct gcatataatc ttatatccca tgtggaaata aa

#tatctgtt  62400

cttggtgctt catctgaaac attcatttta ccaatctatt accctgtaat ga

#aattacta  62460

attagaattg ataatattat attatttcaa ttatgtaaat gaattaaaat ct

#agaaattt  62520

caatgaatag attgtgcatg acattcaaat actatgaaca caattttaaa gt

#tcaactaa  62580

aaatggaaaa tattattgag cttcaaggag actggagaca taaatttgga ac

#agaactac  62640

caaacttgtc ataatttcat aagatagatt atctgaatat ggattcatct ga

#actataac  62700

aaagataaag aggaagaaaa gtgtctgtga ttcagaaatt cacaatggta ag

#cattttgt  62760

gaatctgttc tcttaagcta aatgtcatag taaccaaggc ttgtgtactt ca

#tgacagca  62820

agattacata ttaaaatgga agtttttcaa ttcacttctg tcattgtact tg

#taatgctg  62880

gcatgataaa tatatattct caacatattt gtaaaatatt gtccagaaag tg

#tctaaaaa  62940

atagagtgct tttggagagg gcctgcaaaa ggagagtatt ttcactgatt at

#taggaact  63000

atctctttaa gccctggtta attagtatgt gagttattaa ggcaatataa gt

#aatatagc  63060

taataatgca aagatagaag tttgctaagg aatttgttgt ttccagttat ga

#ttctacaa  63120

gggctttcct cagatagcat aatgatttaa atttgatttt cttaactaat ta

#tttgttga  63180

aaatacagtc catattccaa atggaaatac cttatttgtc tatttctgat ta

#taacagta  63240

ataaatgttc tttggaattc cagtgctatt gaaaattagg ctagccagat ct

#tctttctc  63300

ttaacacagt tctcattgac caccctacaa catccaacat tattgacttc tt

#attctttt  63360

taaattcttt tctactttgt tcctggttat actactctct ccgtgagatg ta

#tgttccat  63420

gaaggcagag gctttttttc tgtttatatc tgtcttattc actacttagt at

#ggtatctg  63480

acaaaagaaa ggtgttcatt aaatgtttgt gtaatgtatt aatcctttta ca

#tatttatt  63540

ccttttccga ttcttttgtt aacttatttt ccttctgcca aatcttaaac ct

#tattactt  63600

ctccagtgtt gagtcttctt ctctctcaag actttcattt tgagtcatca tc

#atcattgt  63660

aatcatgtga tatctttagt taaatgttat ctatgtctct atctctgtcc ct

#gctctctc  63720

ttccagaatc caatctcaaa tctccaactg ccttatgacc ttcttcatat ga

#tggtccct  63780

tagtcacctc aaagttagca tatgcaaaag ttatctttgg agcacccaac ct

#acaatgct  63840

ggctctcatt ctgacaactc tcttttaatt aatggcatga ttattctacc tg

#cttcaatt  63900

tgtaaagctc tctatttctg gtaggtaatt ctatatcatc attataacca tc

#acccccta  63960

tctctaatat aatcatcagt aatattatgt gattcttttt ttttttttga ga

#cggagtct  64020

cgctctgtca accaggctgg agtgcagtgg cgcgcgatct cggctcactg ca

#agctccgc  64080

ctcctgggtt cacaccattc tcctgcctca gccttccgag tagctgggac ta

#caggcacg  64140

cccgcaccag gccggctaat tttttgtatt tttagtagag acggggtttc gc

#catgttag  64200

ccaggatggt ctcgatctcc tgacctcgtg atccgccctt ctcggcctcc ca

#aagtgctg  64260

ggattacagg cgtgagcccc cgcgcccggc caatatttat gtgattcttt at

#tgcttgaa  64320

aagtattttt acatctataa tttcctcttt tggggcttgg tccaatcttc tg

#ggagacta  64380

attctggcag gtagaaatat aaggaggcca atatcagtac attgcttatt ca

#ccattgct  64440

agcgtcttac tcctgggttt actctgactt tggtccccag ctctccagtg ct

#attatttc  64500

tttgcttctt tctgttatcc atattcctgt cttgcaacca agtttccctt ta

#atgagata  64560

ttctatttca ctccagtttt cctatgatgg aaccactttg ctagacaaag cc

#tgcgcatt  64620

tggacttgtg ctcattacat gatgcaaact agtgtgataa acctagttat tg

#tattttat  64680

taacttctta caaaacagta ttcatgactc acttgttcct ttacttctgc ct

#gcagatct  64740

gctttttgga atttcatttt tgtactactg acccttggat ttgcttacaa aa

#ctaaatta  64800

ctgttttttt cttgagcttt tgaatttttg atattgactg cttccagttt gg

#tccacact  64860

aatttcaacc agtcatcaat tattaaagat ataatcctca tttaaaatgt ta

#tatatctc  64920

tatatatttt aaatatgtag tataatttta tatatgctta tttttatttg ta

#tatataaa  64980

tatatacata ttatttacca tatattatat atacatgcat aggaaaggac tc

#tttctggt  65040

tccctagtat tggaattttt gcttttcttc tctctggtat tttttcatcc tt

#gtttgatt  65100

cagacaacct ggctattgtt ttactgctta cccgggatct taatgcttca gg

#ttcggctg  65160

gattccagct tttccttggt tttaattcta attcatatat atatatatat at

#atatatat  65220

atatatatat atatatgtat aatctacatc tgcatcaaat ccctctctag ag

#catgcagt  65280

ggatttcaga cctgggattt catcttgaac ttcagctact gaggatattt tc

#ttgcatta  65340

ttctatttct aaattattct attagaataa ttctattaga attattctat tt

#ctatatta  65400

ttgtatttct aaatccattg cctaaaccaa accattaatt ttgtctcagt aa

#tcctggat  65460

ctttttcttt taccatatag tcaaaaatat tatgtcctta atgctggtgt gg

#cctgactt  65520

aatcccacct cttcttgtga aaacctcctt gaccgtgtag ccttcatttg tt

#tttacacc  65580

tctttaccct tatagcacta agcaccagac atgttagtgc ttaattatta tt

#gtcttaca  65640

ttgtctgtta ttatgtattc atcttatttt taaaaccaga ttataagcaa tt

#taagaaca  65700

ataaatatgg tatagcattt atgtgaactg gaatagatac tatcctacag tt

#aatgaatt  65760

gaccaagcaa ctattcaaag tacagccagg ctgaagacgg cagtatgttg tt

#tttttaaa  65820

agatacttta tttgctcaat aaatctagga agaaatcagc ctcacatttt tt

#tgaactgc  65880

aacttctttg cttgccatca tttaattagt tgccgagtta aaggaccctc tt

#ggctaata  65940

agatagcaaa attgtcatgg attctcatga atctcaatat aattgaactt ac

#aattcatc  66000

taaattattc cactttgttt tttatactat ttgcagtaat ttcattccac tt

#gaataata  66060

agggaatgtt ttctcatgtt ctgtaaatat attatttgag gatattttac tt

#tttttcta  66120

tatttatgta ttggtctgtt ttcatgctgc tgataaagac atacctgaga ct

#gggtaatt  66180

tataaagaaa aagaggttga atggatcaca gttccatatg gctgaggagg cc

#tcacaatc  66240

atggcgggaa gcaaaaggaa ggcacatctt acatggcagc agacaagaga ga

#ataagagc  66300

caagcaaaag gggtttcccc ttataaaacc atcagatctc atgagactta tt

#cactacca  66360

cgggaacagt atggggaaac tgtccccatg attcaattat ctctcactgg gt

#ctctgcca  66420

caacacataa gaattatggg agctaaaatt caagatgaga tttgggtgag ga

#cacagccc  66480

aaccatacca atttctttct atagaatata catttaaaaa ttgacataag tg

#tgctaagt  66540

gctctgcaca tttcagctcc caaggaatgc atattgtagg aactaaagca aa

#aaaaaaaa  66600

aaaaataaca acaaccaggg cagttttatt gagttcagta aagaatatgt tt

#ccctatat  66660

tttaataacc acatctattc ttatctgatt tactttaaga atctattttc ct

#ctttaatg  66720

cagttaacta atactatttc ttatacaatg gcagtttgaa atattaatcc aa

#acattttt  66780

acaatttttc catccatttt cataacatgc cagtgttata tttagtttaa ta

#ggctaagg  66840

ttacctttca tattgatgga tttactctga acttctagct gctcttaagg ta

#gttgtgag  66900

gttttttttt tttcctgtta ttgtaattac agttacagaa taagactgga aa

#ctttgagc  66960

aagtttattt tctgttttta aaaaaaaccc agaaacaaac aagctgacat gt

#tgatgaga  67020

tatattttat taccctactt tacccagaaa gctatgcata aagttcatac aa

#caagataa  67080

aattttaaaa aaaagccaaa agtgtacaaa atacatcttg gcttcatctt tt

#aaataaat  67140

taatatttgt taaacctttg atatttactg aggatatagc agtgaataaa ac

#aaacatgg  67200

tttctgccct tatatttcat ccattctagc aaaaagatag atgcaaaatc aa

#ttattgca  67260

caattaatta ttagttgcaa ttgtgataag tagatcaaga gatgtagggt gc

#tataagtt  67320

aggatagcag gggcctgatt tgtttgtata tgaatatgct tagatgtgga ta

#tgtatgtg  67380

ttcatatgtc tgttttacaa agatgattag gtaggtgtgc caaagtatac ta

#catttaag  67440

cagagagtag atgtctaaga cagctacaag attctgaggt agggaagagc at

#gatatttt  67500

taagagtctt aaagaaggct aatgtaccta gactgtaata gcaagggaaa ga

#ctggcaga  67560

agatgaggct aatgagttag gcaagagtta ccacagatat ttatttacac ag

#aaatatga  67620

cactatatta tcattgtgtg tttatttttc acctttgccc tctgaaatac tc

#tcaattat  67680

gacttagttg taatctaatt atttcaataa cttattaatt ggtttatttt ca

#tatatgaa  67740

atgattaata ttatagattt cagtaattgc tctatagctg ttactgattt ac

#tcattctt  67800

ttgtgtttta aaaagtttaa aacataccag atgttttatt gaactaacat tg

#aattcatg  67860

attttttttt atgactaagg cttcctcatc attcaataaa gttttataat tt

#ttatcaca  67920

aatatgctac ataattttgc tggatttatt cctaatatta tatttttctt ct

#aaggtaaa  67980

tgaatttttt tctggctaga ctaatagttt ttgctgccct ataggaatag ta

#tggatttt  68040

ctttttaaga cctagtaaag atttctaggt aaaaatcata taatctgtac aa

#aatataat  68100

gaaaaaggaa ataatgaaag caaaatccca agaattcttt tttcccccct ca

#aagaatgc  68160

gttgaagaat gggcaaataa aatcgggaat atttagaggt aggaaggtgg tg

#aaaaggtt  68220

cacaaagaag tttcaatttc aacaaaaagc ttttaattca aagatttttc tt

#tctttttc  68280

tgagagtgat cagaacatga agatggctgt tgggagacaa atctccatgt at

#cctttatg  68340

ttcccaaaca tcttttgggc aaaggcacta agtgcctttg tgcctgtctg tc

#tttacaag  68400

tatgtttata tcgtgaacac actaggaaga tatagatagt gtctctctct gg

#agcaaagg  68460

gtaggttttt tatctttata cagtaaagat aatgtctcct tatggggcaa ca

#atcagtga  68520

ggattattgt ccattatgaa agacctgagt tccttacctt ggttctcccc tg

#tcacatat  68580

cccgctacat gtgcagcatc tcctggccct ttgcacaccc ttctgtggga gt

#tggggctc  68640

agaatgcaac acaaatgatg atactctagg tactactatt ctgtgcataa ta

#aaccatct  68700

tttgtctctg actcaagagt ctcatggctt ttgctagcat ccataaaact gg

#cagggcaa  68760

atcctgatac ccttcacaat tcttggcagt tttggcagtg aggaagggat ac

#tgacagag  68820

acatggcttt tggaaaaaga aggatgatgg cctcacagct aattaataga ct

#ttgaaaga  68880

agtccattgg tattggtagc aaacttgtgg accaaattgt ctagtaagca ga

#gcaataaa  68940

tattcttcta ctctattgct cattaatgag gaggatttgg ggaggtagtt gc

#aagctgag  69000

aaccaggcaa cagatatgat ttaactgtcc tttaggcagg gagattacag tc

#tggcagta  69060

gtctcaggtt cacctattgt aacaattagt acttagattc atttgggctg tg

#gggtgggg  69120

agagaggaac aagtttgcat tttctttttt tgttgttgtt gttttgtttt gt

#tttgtttt  69180

gtttttcaga cagagtctca ctctgtcgcc caggctggag tgcagtggcg cg

#atctcagc  69240

ttactgcaag ctccgcctcc cgggttcacg ccattcttct gcctctgcct cc

#cgaatagc  69300

tgggattaca ggcgcctgcc accacgcctg gctaattttt tgtattttta gt

#agagacgg  69360

ggtttcaccg tgttagccag gatggtctcg atctgctgac ctcgtgatcc gc

#ccgcctca  69420

gtctcccaaa gtgcagtgtt gggattacag gcgtgcgcca ccgcgcccgg cc

#gcattttc  69480

tttcagacaa caattttaga gatacatacc tacagtgagc atgagaggaa aa

#tttatgac  69540

tattatgtac agaaaccagg caaattatta gaactttggc tgattttctt gg

#aaaatgag  69600

tgaggtgggt catggaatgt tggtaataga agaatggcca aaactgggat at

#cttttttg  69660

ctcagactct cctaccatca tgccaacttg taatccatct ggagatgaca gt

#agaaagtc  69720

ttggaatttt ctgtaatggg ttctatctgc tgtaaaataa ctttggccct tt

#tatggaga  69780

tttctctgga agagacaaaa tcaaggggaa actatagatg aggcattaat ta

#gtattgca  69840

ctcttacagc cccagattgg tttcataatg ctaatataag tgaccccctg ga

#gaatgaaa  69900

aggtcatcaa agaaatttag ataaattctt gtggtcagcc tgaagttcta ga

#aaagttct  69960

ttcaccctta tgttggaacc aggcaagaac ttaataaatg ttgtattgat ag

#tagggcag  70020

caggtacatc tatctagtct gaggatgttg ttgctgttac agccaattag tt

#tattctag  70080

acacaccatg tgacccttga aactaatcta tgttatgtat tcagatttct ga

#accattca  70140

cagtcagaga gtcatgcact ttttaatccc caaagccata caacaattgg ct

#gataatca  70200

aggtatgtga tagaccttcc acatttccta tcatccatcg gcatctggta tt

#gttaaatg  70260

ttggaagggc ttcttcaaaa attaaaaaaa gtttccaact ctgcctctct ca

#cctccttc  70320

tggtgcacac atataagtaa gatggtttgg tcactgaatg tggcttctgc ag

#aaactgat  70380

catctcctct cagcctctat gtggataata agatgaaagg gttaagattt ta

#tataaact  70440

tatattgaaa aatcagtgtt ccaccatgac catttctggg cataatgcgt ta

#ttctttct  70500

tattacagaa acctcaggcc agcctgattg gtacatcctc caaatggtag tc

#cagctaaa  70560

gggaggcctc aggaattttt atttaattct tgtatagcta actggatatg ct

#tgttggct  70620

tcatttggtc ctacattgta agagtagtaa ccatttagtt gagtacacag ct

#tgccaaga  70680

ccccctgcaa ttgcccaaat gtaccattaa tgtaggggac ataatgagtc tc

#tgtaaatt  70740

ttataaaaat gcccttttct cccttattct gacccttccc aacaaaagat tt

#gggtatga  70800

tagaggatgg ttagaaaaaa agtgaaatta tagctaccgg aatggaacac ac

#tctgcatt  70860

tcaggtgcag gagtaaaatc aatgatcttt cagaacttcc cctggagcct cc

#cacataaa  70920

gaaaagtcct tggtgtgagt ctctcaaact gtggtaaatg ctttaaatgt aa

#tttccttc  70980

tggcttaaca ttcttcatca gatgtctctg cctgcatttt gatcatcatt gc

#ttttaacc  71040

ttgaggagaa gtttattaga aacatcaggg aaagatcctt tatcgcctac ac

#acacacac  71100

acacacacac acacacacac acacacacaa aacctattaa cacctttggg tg

#tcttcttt  71160

acccctcttt ctataaccat caatcactca ttccatgggg tggatgaatg cc

#atgtagtg  71220

gcttgcatgg ataaatagat cagattggac tgactgtccc caagcagttt ct

#ctaaaaaa  71280

cagcaataat ctcaattatc tgaactgaac tgagaacccc aaggccaact ag

#ctggcctg  71340

gaggccctgt tggagacatt gccaatctgt ttcttctaac tgacatcggt cc

#atttttgg  71400

ggtcacagtc atcgtaaata acatgttctt tctaggacca ttgtgtgaac cc

#ttaagact  71460

atatgtcttt tttttttttt ttgagacgga gtcttgctct gtcacacagg ct

#ggagagca  71520

atagcgcaat cttggctcac tgcaaccccc acctgctggg ttcaagcaat tc

#ttctgcct  71580

cagtctcctg agtatctgag actacaagca cgtgccacca tgcccagcta at

#tttttgta  71640

tttttagtag agatgggatt tcaccatgct ggccaggctg gtcttgaact cc

#tgaccttg  71700

tgatccgtcc acctcggcct cccaaagtgc tgggattaca ggcatgaacc ac

#tgcgcccg  71760

gccaagactg catgtcttat gtccaaatca tgcattattt tccctcccta tc

#caaaatat  71820

agtgacttga accacaggga tggtcataag agacctttga atgtttaagc aa

#acaccacc  71880

agtagattat gtaagcttca gacgatttcg gagagaactc caaaatctac ac

#ttggctat  71940

gaggatgagc ttcctggagg gataattgac ttattagttt tgtgtgccct ac

#aggcagtt  72000

atccctacaa tggtaatcat caaattagaa aaattggtga gaaatttgcc cc

#tgaattta  72060

atctaaaaga ttaatgatac aattccagtc ttctttagcc tcagttcatg ga

#ctaacgtt  72120

tttatggatg ataggattgc cctcagctac ctccttgtgg tccaaggaag ag

#actgtgca  72180

attgcttata tatcctgctg tacctgatct aatgcctccg gccaagtgga aa

#ggttaata  72240

tagaaactta aggagaaagt cacatggctt tgtaagggaa acctttatgg tt

#tgggggat  72300

ttattcagtt tgttgggttc agcagctgaa tacatcagca gtgtggttga gg

#tatatact  72360

gtagattggt cccatccttc tgctttgagt cctgttgata gtgaccttaa gt

#aaagacat  72420

gtatgagaca aagtggatga acttttttcc agcatctgtt ggttagattt at

#ccgtgact  72480

gatggcgtat ttatgggaaa attagtcaga gaaaagatga tgtcaagaca ag

#ctgtggct  72540

attgttgatg actgttctca gttgattctg ctgtcactat atcagaagcg aa

#gagaaaga  72600

gtatgaagca aacagacaga aaactatgga agaaataatt gaagacagtt gt

#ggtggctc  72660

atgcctgtaa tcccagcact ttgggaggct gaggcaggca gatcacttga gg

#tcaggagt  72720

ttgagaccag cctggccaac atggcaaaac cccatctcta ctaaaaatac aa

#aaattagc  72780

tgggtgtggt ggtgcatgcc tgtaatccca gctacttggg aggctgaggc ag

#gagaatca  72840

tttgaacctg ggaggcagag gttgtagtga gcagagatca caccactgca ct

#ccagtgtg  72900

ggtgacagag tgaaagaaag aaaagaaaga aaaggaagaa aaagaaagaa ag

#aaagagag  72960

agagagagag agaaagaaag aaagaaagaa agaaagaaag aaagaaagaa ag

#aaagaaag  73020

aaagaaagaa aggaaggaag gaaagaaatg aaagaaaaga aagaaaagaa ga

#aagaaaat  73080

ttctggaaaa aaaaaaaccc cataaactta cacattgaag aagctcaggg tt

#cccacagg  73140

ataaatgcta aaataaacaa acaccaaaac aaaaccccaa atcccaaaat ta

#ttaaaaag  73200

tatcataacc aagcttctga aaactaaaaa caaagaaaat attctaatag ta

#gccagaga  73260

aaaatgcaac aatgattcca atgattgcag atttctcatt aagaaatatg ag

#ggctaaaa  73320

ggaaatggaa cagcatttga gaatgctgaa agaacattta gtccaggatt ct

#atatccac  73380

tgacatattc tttaggcatg aaagttaaat aaaggcattc tcagacaaag gg

#aaactgac  73440

atcatactta ttcatgaaag actgttttcc ccctgtgacc aggaacaaag ta

#agcctggc  73500

cactctcatc actgccactt aatatcgtac tggaattcta gccagtataa ta

#ataaataa  73560

ataaatagag aaagagcttg gaaaggaaaa aataaaatgg ttcatattca ca

#tatatatg  73620

atctctacct ggaaaattcc gtggaaccta caaaaaaatt agaaataata ag

#taagttta  73680

ataaggttga aggatacaag gtcacatgaa aataaatcac atttctctac ac

#tagcatta  73740

aaaattggaa acaaattaaa aaatataata gcctcaagaa atgaaatatc ta

#ggtataaa  73800

tttaacaaag caggtagaag atctgtgttc tggaaattat aaaacctgat gg

#aagtaaat  73860

attttgaaat gaaagaagac ctaaataaat gaagatacac atagtttcca tg

#ggttggaa  73920

aaatcattac acttaaggta ctattctccc taaattgatc catagattta gt

#gcaatatc  73980

aatcaaattc caagcaggaa ttttgtagat acagaaaaac ttgttctaaa at

#gtatatca  74040

aaaggcaaaa agattagaat agccaaacag ttttgaaaaa gaagagcaaa gt

#tgggagac  74100

tcataccatc tgactttaag aattactcta aagctatagt aatcaaaaaa gt

#gtggtatt  74160

gtcaaaggaa tagacaaagc aatgaactaa atgtttgtgt tcccccaaaa ct

#cataggtt  74220

gatattctca ccccaatatg atggtattag gagatcgggc ctttgggatg aa

#attaggtc  74280

atgagggtga agcccttatg attgggatta gtgcccttat aaaatgaacc tg

#ctctctca  74340

gccttttcca ccatgtgata ttacaaggag aaaacagcag tttgcaaccc ag

#aataagtc  74400

cttcactaga acctaaccat gttggcaccc tgatttcaga catccaggct tc

#agaactgc  74460

aagaaataaa tttctgttgt ttataagcca ctcaatctat ggtactttgt ta

#tagtatcc  74520

tggactgact gaaatatagg cctagatcaa tgggacattt tagaaagtcc ag

#aaaaacag  74580

tccaaacaaa tataactaat tgatttttga aaacggcaca aaccatgaag aa

#tatacttt  74640

ttctgtgtct tttatttggg tcttttccat aaatggtatg atattggaac aa

#tttaacat  74700

ccatatgcaa aaaataaaaa aaaaaccctt gaattaaacc tcatatctta ta

#ccaaaatt  74760

aactcaaaat ggaccatagc ttcaagatgt aaaatataat atatgaaact tt

#agaagaaa  74820

acataaaaga aaatctttgt gacctttagg cagagagttt tcaaatttga ta

#ccaaagca  74880

taatttataa cacacacaca caaatcagaa tttatcaaaa tttaaaactt tt

#cctcagtg  74940

aaagacactg ctaaaagaat ataaagtcaa actataaatg gggagaaaag ac

#aaatattg  75000

caaatcatat gttcaaaaaa tgtcgtgtat ccagaatgta taaagaagtc tc

#aaaactcg  75060

acagtaagga acagacaacc caataaaaat aagcaaaatg ttttcataaa ca

#ctttgcca  75120

gagaataaat atggatgtca aataaactca ggaaaaattg tcaacaataa cc

#attataga  75180

aatgtaaagt aacaccacaa tgaaatacca ctacatagaa tggctacaaa ac

#aactgata  75240

ataccaagtg ctggtgaaga ttcagaacaa ctgcaactct cttgcattgc tc

#ctgggaat  75300

gcaaaatggt acagccattc tggaaagcag tttggcagtg tctcagaaag ct

#gaacataa  75360

acttatcata tgactagcaa tcctacttct aggtatttac cctagagaaa ta

#aaatttat  75420

gtttacacca aagcctacac aagaatactt atagcagttg tatttataat tg

#ggccaagc  75480

actagaaacc caaatgtcct ccagcaggtg aatgcataag caaagagtgg ta

#cattcctg  75540

caatggactg ttactcagct atgaaaaaga atgaactact aatacacaca at

#gacagata  75600

aatctcaaaa tctcaaaggc atttgctaag tgaataaagc cagtctcaaa ag

#gttatatg  75660

ctgcgtttcc acttacatga cattttgcaa aggcaaagct agcagcagag ac

#cagatcag  75720

tggttgctgg gggctacaaa agggaggtag gaatgactac aaaggaggat ca

#caagggag  75780

tttttttggt gaataacatt ctgcatagtt ttagtataaa tgaattttat ca

#tgatctac  75840

tcttctgaat attacccata aaatatacca tatatgatga gagaaaatga gt

#atatgtgt  75900

ctgagaaata gaaatagtct ccatgagtgt taaaaataat ccaaaataat aa

#tcatattt  75960

tatttattat ttattatatg tatacattaa tatatacatt ttacatattt at

#tttcccca  76020

attatactgg acttcatgta atgatgaatt tggttttagt tcctgagttt ga

#tttggatg  76080

agtgttgcag tggggagcag gggaggtgtg agcttggggt ggtgcgagct tg

#gggtggtg  76140

ctgaaggcag tgactgggac attttaagct cagggtcgtg gtaatacatg tt

#catggtaa  76200

tacatgtctc tgatttttta gacaccccat cacagagggt acagtttatt ct

#tggaaccg  76260

aggatgatga cgaggaacac attcctcatg accttttcac agaactggat ga

#gatttgtt  76320

ggcgtgaagg tgaggacgct gagtggcgag aaacagccag gtgaggattt tt

#gttaaagg  76380

gtgaaggtat actaaagaat tttcatgtta ctagaaaaag agatttctaa tg

#caacaatt  76440

ttgcaaacat ctatgattgc tgctgatttt agaagttgct catctagcct ga

#gcatatcc  76500

tataacggga tatgggtcag aaagaaatct gaaggcagta attacagtaa ac

#ggtgatgc  76560

agagccagca acagctgcag tcttaaagat aaacagtaac ataatttgtg tg

#tcatcaac  76620

aaaacaaaag aaatctaaaa gtagtttatt tctatttttt cagctgctgg ct

#tgcaccta  76680

aatttatgat agtatatgat aacttgaaag tgggcttttt ttaaaagaaa gg

#gcaaatat  76740

tatgataaaa tgctttatgt acagtcctgg atttcatgtg ctctttcatg ag

#gataaaaa  76800

taatttgtaa tatgtttcta ggatatgcat acatttaagc atagtggttt tt

#aaaaatat  76860

cttttaaaat cactttttct atcatttgta attaagattt ttacattgct at

#ataattga  76920

tagagttctg taaagttgga attaaatttt gtgtttactt ttcattcatt ct

#ttctgatt  76980

tgctcagtta acaaacattt atggagtgtc cattatgtgc caagtgcaat gg

#atatggca  77040

caacaacaaa aatcttagat cttgccttta gggatcttgc agtctaattt ag

#acaagaaa  77100

acaaagttgt aaatgctgta taatgaaagc tgtgatacag gtgtgcacaa ga

#aactgtgg  77160

gcacacccag ggttgtcatt tacccacttt ttcacaaatt ttaatgtgac ta

#ccaatcac  77220

ctggaatatt gtttaaaatg tagacttagt aggcctcagg catagtcaga cc

#atgaggat  77280

gtcgtgtaaa atgttttggg tttgagaacc aaactttgag tagcagttat ct

#aaaccacg  77340

aggtgaaaga gaggatcagg gtagcttccc tggaggaggc gattcttgag ct

#agctcttg  77400

tgagttgggt tggagttagc taggcagaaa agcagagggg acagtattct ag

#gcagagat  77460

agcaggacgt gcttaaatat atcattgaca caggtttagt gtttatttat tt

#atttattt  77520

atttgtctga gacagagtct cactctgtcc cccagggtgg agtgcagtga cg

#agatcttg  77580

gctcattgca acctctgcct ccctggttca agccattctc ctgccccagc ct

#ccctagta  77640

gctgagacca cagtcatctg ccaccgcgcc cagctaattt ttgtattttt ag

#tagagaca  77700

gggtttcacc atgttggcca ggctggtctc gaactcctga cctcaagtcc tc

#tacctgcc  77760

tcagcctccc aaagtgctgg gattgcaggt gtgaaccacc atgcccctgc tg

#acacaggt  77820

tttattgttt tgttaggcta tctcttccac tgtaggacag cattattatt ag

#aaagactt  77880

tatcttaagc atatttatta gtggtcctca gattgcaatt gctgtctgaa ag

#ccacagta  77940

attccattgg atcatgttaa acttgtagct gcatttattc attgacttta ct

#cagtgtag  78000

aaataaatgc tcaattatga aaaagaatgt tgtgaataac aatggcccag tt

#aattcttg  78060

tttgatatat tttcagtggt ctttacagct ctcctttatt taaaaaacac ta

#aaaacgag  78120

acaaccaaaa tggttaccaa ctagtttatc cttattaaca ttttaaagta aa

#taaaacta  78180

ataactgcca gtatttaaaa ttcacaaggt ataggatggc agaaaagtaa aa

#atacttct  78240

ctatgcttat tcacagtatc tcttttcaaa agtaatcact gttaatcttt tc

#tgtgcatc  78300

tttcccccaa aatttaatag ctaaatctgc gtgtaaatat atgccctttt aa

#atttacac  78360

aatagggatt atataatata cagtgttcat atcttatctt ttccacttca ta

#tatttgga  78420

acattttcca tatcagcaat tcaaatttat atcatctatt tgatgattgc at

#tgcattca  78480

attatatgga tgaactttca tttatttatt tatcagttag tcttgataga ca

#tttaggtt  78540

atttattttt ttccataaaa accactgcag tgattgctca cacaaatatt tt

#gtcattat  78600

tttgtaggta tttctgtaaa gtgaatttct aacaatggca acatatgtag ca

#aagagagc  78660

agacattttt tcctttgata aatactgtaa acttaccttc ataaaatgtt tt

#tctaattt  78720

acacttctat caacagtgta tgagagtgct tatttcctcc acatcctttc ac

#agtaaatt  78780

atcaaactgc ttaaaatgtc ttttccagtt ttataaataa aacataaatc tc

#attgtttt  78840

aatttgatta ttcaaattat tagtgaggta caacatcttt tcctatgttt tt

#attttttt  78900

catgtgaacg aactattcat ttcctttatt tattttatat aaatcattca tt

#attttctt  78960

tatttgcctt ttggaacact ttaaattggt ggcatgttat tcagtatgaa ct

#aacctttt  79020

taataaaata atttacataa gtttcctcat gatgttttgt attgtaatac tt

#taaatata  79080

gacttaaatt taaaatagtt tttatttaac ctggtacata ttaagattaa ga

#gacttcta  79140

ccttactttt tgtcccaact gcatcaaaaa ctacgtagta gttttaaaaa tg

#tgtaatat  79200

atgtgctcat cttctttatt tggtgacaga aagggaatat aagatcattt tt

#tccacaga  79260

ttagtgatat aacttgctct tttatgattt tgataagtta aagttcctcc ct

#ccctgttt  79320

aagaccagaa gcatctgtct gccacgagtt acaaggaaca gatgttccta tg

#tgacttga  79380

aggaaggcga tctggtgatt gtgatgacta gacagctctg gttagttaga gt

#ctctttaa  79440

cctattgcta agaagtattt tgttgaagca tttattttag agttccttct tt

#accctcat  79500

actacataat agagctgaaa agtaaaattg gaatatatat ttgggcaaga gt

#aactcact  79560

tattcttaca gtgattggtg atttttcatc ttacagatca aatagtgacc ca

#ttcatttt  79620

aaccaataat ttcttgtaac ttgcccactc tcataaagct aggagattgc ag

#aagcgata  79680

ctagaatata gcactctcac tttgttacag ttgagcaggt aggtttttgt ta

#tgctctaa  79740

tggattaact caataacatg tttgtcctaa accatcaaaa tatattgctg tt

#gatttata  79800

aagaataaaa agatagtcca tttaattata cacattctct aatattatta ga

#tggaccta  79860

tgtttgtagc caagcttcta gaatctaatg catgctatag ctgtttgagc tt

#cagggaga  79920

catctgatga gcaatggaaa taataacaga tattgaaggg gagggtagat ga

#attttaac  79980

agagacacaa tgattcaggg aagggcagaa catatttatt gaggatttcg aa

#aagtaaca  80040

ggttttaaag tggcagaagt aattttgttc tgattgccct aattcatcta aa

#aacactaa  80100

tttttgttaa ttcatgactc catctgattt ttcacatgca atttaattct ag

#aaaatcat  80160

tagcatcacc atttaaagca cttctttctt ttgattagta ttccagatgg ga

#ttaataat  80220

tttctaccct cacagcagaa acaaaaagat attttatcag ctcattccac ct

#gtcacgta  80280

tcacatcttg cataatttat gcccactgtc attgccaagt aaaacttaag ca

#aagtttta  80340

ggttttgaag ctaaattttt gaatcataat tatttaataa atgttcgtaa aa

#accagctg  80400

gtcactttta aaaaccctaa aagaagccat atgaagagac taatgaaatc aa

#cacaatta  80460

caatgtcctg cttataaata acatgtaatg ttattaatag aaaagtgagc aa

#agctacca  80520

cagctgtgca gttgtggcga caacatgttt gactcactgt agttaccctt ta

#taaaagct  80580

tcccactaat gaactcagaa gaggcaaagc agggggtagc gttaggcttc tg

#atacatac  80640

atacatggca gaatagaaaa ggattattac atcagaacaa ttttattgat gc

#tgtgaagg  80700

catttgatct tcaaaattag taatggttta agtcatctgg attttttacg gg

#aaaataat  80760

gtggattaag aacaggtgtg aaaataatat ggattaagaa cagttaatgt ct

#ataaacac  80820

taggtttgga tgtatatcat ttccccttaa gatgactata ggtattcttt ga

#ttacatgt  80880

tattctctag ctccacccca gccatgtccc ccaactatcc taaaagagga tg

#tttttttc  80940

ttgagacatc cattatttcc ccgaaggcta taattttgga tgatataata ac

#tccttttg  81000

gatgatagac ttactctttt tttgtttggg tagaatgaga ggattaaaaa tc

#ttagaaaa  81060

gttaaactga gttagtgaga atagaacacc cagaaagagt taagttctct ag

#aaaaaacc  81120

ttctctagaa gcacctaatt ggcagaataa ttttattctg tatattttaa ta

#ggagtatt  81180

gtagaggaga ttataataaa cttaatcctc aaagaattca tgaaacacct at

#ttaatgtt  81240

gcttagtgga aagagactcc aatgtgctaa tcttggatga aaacagatcc ag

#acatactg  81300

aaggaaatga aaataatctt ctcagggttt aaatccaccc ctctctcccc ac

#agaaaagg  81360

tcgtgcaatt ggccaacagt tttatttatt tattttttag cattatccct ca

#catctcat  81420

tcatgctttg aaactcttgt ttgccttggt ttgctgttca aacaaatgtc ag

#cagagttt  81480

atttgaaaac tggaacaaat tgcagcactt taggtcatta actgcaatca gg

#cattttgc  81540

aactgacagt atattcagtg attacaaatc ttgaaacagt gtctggtgtg ct

#cccagatc  81600

tgttcatgtc tatctttgaa ggatgaaatg ggatttaaaa gaacagaaaa ga

#gagatata  81660

gttatgtatt tatgtgtatg tattattttt aatagtctct ttaacaatat tc

#atttaaat  81720

atctcttaaa gaattggcat cattctggag ctggcataga gcactgaatc tt

#gaaatgtt  81780

tagtatcttt agtaacttga tatttgtaac atgtgggcac ctttttatgg aa

#agtacctt  81840

ctgcctcctc ctataatact cataaaacct atgggtacat caaaccatcc at

#gcatataa  81900

cttatatttg gtcatcttaa ctaacaaact gtttggaact ccctgaagtt cc

#aaactctc  81960

tgaaaagaac tccattcttt tctcagagaa ttaagccctc aacttgaaga aa

#attattct  82020

aaaggaagga agaataattg gattttttaa aatgtcattt cagacacata aa

#tcactgga  82080

acggaataga gaactaagaa atagaccagc acaagtaaag cttactgatt tt

#tgacaaaa  82140

gacaaaaact attaaatgaa ggaaaaataa tctttttgaa aaataatgtt gg

#agcaatta  82200

gacacctaca ggcaaaaaat tagccttgat ataaacctca ccatgtacat aa

#aaattaat  82260

ttaaaatagt ttatagattt aaatttgaaa cataaagcca tgaaattttt ag

#aagaaaat  82320

attagataaa atcttcagga cctagggcta ggtggcaagt ttttagacat aa

#caccaaaa  82380

gcgcaattcg taaaaggaaa tatttataga ttgaacttta ccaaaattaa aa

#tgtttgtg  82440

ctgtgaaaga ttctgttaag tggatgaaaa ggcaagctac agacagaaag ta

#tttgtaaa  82500

ccagatattc aacaaaagtg ttatatgtag aacatataaa gaactctcaa ag

#ttcaacag  82560

tatgaaaata aatcaactag aaaagtgggc aaaaggcaca aacagacatt tc

#accaaaga  82620

agagatacat atggcgaata gcacatggaa aaatgttcaa tatcattagt ca

#tcaggaaa  82680

atgcaaatta gaactgctct gagatattac tgcataccta atagaatagt aa

#aaatgaaa  82740

aaatagtcat aataacaaat gttggtgagg atttgaaaaa actagatctt tc

#atacattg  82800

ctggtgtgaa tgtaaaatgg tagagccact tatggaaaac agtttgacag tt

#tctgataa  82860

aactaaacat gcatttacta tatgatccag caattggact cttgggcatt ta

#tcccagag  82920

taatgaaaac atgttcacac aaagacctct gcatgagtgt tcacagcaaa tt

#tatttgta  82980

atggcaaaac ctgcaaacaa cctgaatgtc ccccatgggt gactgattaa ac

#aaactgat  83040

acatccatct ttataatgga atattactct gcaataaaaa ggaacaaact ac

#tgatacac  83100

acaataactt gaatgtatat caagggcatt atgcttagta aaaaagtgtc aa

#tctcaaaa  83160

ggttgcaaac tatatgattc catttatata acaccgtcaa aataacaaaa gt

#atggtgat  83220

gaagaataga ttagtggttt ccaggggaca gaaatagagt gaggattgag aa

#tataaagg  83280

tgcagcacaa gggatttctt ttgtggtgat ggaacagctt cgtatgttga tt

#gtggtaga  83340

ggttacatct atctatacat gggataaaaa tgcatagaat ggaggcaggg ca

#tggtggct  83400

catgcctgta atcccagcac tttgggtggt cagctaaggc aggaggatta ct

#tgaggcca  83460

ggagttcaag accagcctgg gtaacatagt gagaccccca tctctattaa aa

#aaatacaa  83520

aaaaaaaaaa gccagacata gtacctggct atgtagtccc agctacttgg aa

#ggctgagg  83580

tggaaggatc atctgaaccc aggaggttgt ggctgcagtg agctgtgatt gc

#accacagc  83640

actccagtct ggatgacaga gtgagactat gtctcaaaaa agtttttttt aa

#tgcataga  83700

actgcacaca cacacacata cacacacaca cacacagcaa cacacagagc cc

#acatctta  83760

tcagtattct tttttttttt ctttccaact tttattttag gttcaagggg ta

#tatgtgca  83820

gggttgtttc atgggtaaat tgtgtgttac aggtttggtg tacagataat tt

#tgtcagct  83880

gttaggtagt ttttcaatcc tcccattcct ccaccttacc tgatagatat tt

#tttgtcac  83940

tgaataggta gttttcgatc atcccactct ccaccctcaa ctaggcctca gt

#gtctgttg  84000

ttcccttctt tgtagtccat gtgtatgaat gtttagctcc cacttgtaag aa

#cttgcagt  84060

atttagtttt ctgttcctgc attagttcac ttaggataat ggcctctagc tc

#tattcatg  84120

ttgctgcaaa ggccattatc tcatttttta tagctgcata ttattgcatg gt

#gtatatgt  84180

actacatttt ctttatacag tccaccactg gtaggcacat aggttgattc ca

#tgtctttg  84240

ctattgtgaa tagtgctgca atgaacatac atgtgcatgt gtctctatgg ta

#gaacgatt  84300

tatattccat tggttatata ctgagtaata ggattgctgg gatgaatgat ag

#ttctgttt  84360

taagttcttt gagaaatgtc cagactgctt tccacagtgg ctgaactaat tt

#acattccc  84420

accagcaatg tataagcatt ccccttcctc tgcaacctca ccagcttctg tt

#attttttg  84480

actttttagt aatagccatt ctgactggtg tgtgatggta actcattgta gt

#tttggttt  84540

agatttctgt aatgattagt gatactgagc attttttcat atgcttgttg ct

#acttgtat  84600

tagtatgtct tcttttgaga agtgtctgtt aatatctttt gcccactttt ta

#aatagggt  84660

tgtttgtttt ttgcttgttg atttatttga gttccttaaa gattctggat at

#taaacctt  84720

agtcagatgc atagtttgca aacattttct cctactctgt aggttgttta ct

#ctgttgat  84780

agtttctttt actgtgcaaa agctctttag gtcaattaaa ttccacttgt ca

#atttttgt  84840

ttttgttgca attgcttttg gcatcttcat catgaagtct tttctttggc tg

#atgtccag  84900

aatggtattt cctggatttt cttctagagt ttttatagtg tttttggcct ta

#catttaag  84960

tctttaattc atcttgagtt gacttttgta tatggtgaaa tgtaggggtc cc

#gtttcaat  85020

cttctgcata tggctagcca gttatcccag cagcatttat tgagtaggga gt

#cctttcct  85080

cattgcttat ttttattggc tttgttgaag atcagatggt tctacatatg tg

#gctctatt  85140

tctgggtcct ttaacctgtt ccattggtct atgtgtctgt ttttatactg at

#accatgct  85200

gttttggtta ctgtagcctt gtagtatagt ttgaagtcag gtagtgtgat gc

#ctccagct  85260

tcattctttt tgttcaggat cactttggct atttgggatc ttttttggtt cc

#atatgaat  85320

tttagaattt ttttctaatt ttgaaaaatg tgcacttttt tctaattttg ta

#aaaatgtt  85380

attggtaggt tgataggaat agcactgaat ctgtaaattg ctttgggcag ta

#tgccattt  85440

taattttgat ttttttccta tccatgagca tggaatgttt ttccatttgt tt

#gtgtcatc  85500

tctgatttat ttcagcagtg tcttgtaatt ctcgttgcag agatctttta cg

#tccctgtt  85560

tagttgtatt cctaggtatt ttatgatttt catggctatt gtgaatggga tt

#gcattctt  85620

gatttagctc tcagcttgaa tgttattggt gtatataaac atataccatt tg

#catattga  85680

tttttgtatc ttaaaacttt gctgaagttg tttagcagat ctaggagcct ca

#agcagaga  85740

ttatggtttt cctaggtata gtatcatatc atttgcgaag agagatgatt tg

#acttcctc  85800

tttctctatc tggatggctt ttatttttta ttcttttctg cttctctggt ta

#ggacttcc  85860

aggacttatg ttgaataaga atggtgagag tgggcatcct tgtcttgtac ca

#gttttcaa  85920

ggagaatgct ttcagctttt gcccattcag tatgatgttg gctgtaggtt tg

#ttgtagat  85980

aacacttatt attttgtggt gtacaccttc aatgcctagt tttttgcggg tt

#tcaaacat  86040

gaggggatgt ttaattttat caaaagcctt ttctgcatct tctgagatga tc

#atgtggtt  86100

tttgttttta gttctgttta tgtaataaat aacatttatt gatttgcata tg

#ttgaacca  86160

aacttgcctc ccaggaataa agcctatttg atcatggtgg attagctttt tg

#atgtgctg  86220

ctggatttgg tttgctagta ttttgtggag gatttttgca tctatgttta tc

#aggggtat  86280

tggtctgaag atttttgttg tgaatctgcc tggttttagt atgagaatga tg

#ctggcctc  86340

atagaatgaa ttggacagga gcccctcctc cttgtttttt ggaatagttt ca

#gtatccgt  86400

tcttctttac acatctggta gaatttggct gtgactccat ctgatccaag gc

#ttttttct  86460

ggttgatagg ttttttttat tactgattca agtttggaac tcattattgg tg

#tgttcatg  86520

gtttcaattt ctttctggtt aggccaggta cacggctcac acctctaatt cc

#agcacttt  86580

gggaggttga ggtgggtgga tcacttgagc ccagacattt gagaccagct tg

#gccaaaat  86640

ggcaaaaccc tgtctctact aaaaatacaa aaaaattagc tagacacagt gg

#tgtgcacc  86700

tgtagtccca gctacttgtg atgtgaggca ggagaatcac ttgagtgcag ga

#acagaggt  86760

tgcagtgagt caagattgtg ccactgcact ccagtctggg tgacagagca ag

#actctgtc  86820

tcaaaaaaat aaaataaaat aaaataaaaa taatttattt ctggtttaat ct

#tgggcagt  86880

tgaatattcc caggaattta tccatttctt ctagcttttc tagtttgtga gc

#acagaggt  86940

gttcataata gtctcttagg gtttttgtat ttctgtcggg ttagtagtaa tg

#tctccttt  87000

gttttctgat tgtgtttatc tttatcttct cccttttaaa aaattagtat ag

#ctaatagt  87060

atatcaatgt tatttattct ttcaaagagc caagtcttgg ttttgttgat ct

#tttgtgtg  87120

atttttctca tctccatttt attctgttca gctatatttt ggttatttct tt

#tcttctgt  87180

tatatttggg attggttggc ttttgttttt caaattcctt caagtgtaat gt

#taggttgt  87240

taacttaagt tgtaagtttt tcttttttat gtcgacattt agcagtataa ac

#tttcctct  87300

caacactgct tttgccctgt cccagagatt ctagtatgtt gtatctttgt tt

#tcattagt  87360

ttcaaggaat ttctcggttt ctacagttac ttcattgttt acccaaatca tt

#caggagta  87420

ggttgtttag tttccatgta attgtatgct tttgagagat cttcttgata tt

#gatttata  87480

tttttactgc attgtgttct gagagcatgt ttggtatgat tttggttttg ta

#aaatttgt  87540

tgagaattgc tttatggcta agtatgtggt caattttaga atatgtgcca tc

#tgcagatg  87600

aaaagaatgt atattctgtt tttgttgggt ggagtgttct gtagatgtct gt

#taggttca  87660

tttggtcaag tgttaagttt aggtcccaaa tatctcttgt tagtattctg cc

#tcagtgat  87720

ctgtccaatg ccatcagtag ggtgttgaag tcttccatga ttatattgcc at

#tatctaag  87780

tctcttccta agtctctaag aacttgtttt atgaatctgg gtgttccagt at

#tgggtgca  87840

tatatattta ggatagttaa gtcttcttgt ttaattgaac actttatttt ta

#tgtaatcc  87900

tcttcttttt actttctgaa tgtttttggt ttaaagtcat tcttttctga aa

#taaaaaca  87960

gcaacccctt tttagcattc ttaaaattta aaattttact ttcaaaggag cc

#aagatgaa  88020

atgatttaga tgctttgtca cttatttagt catcttcact gttatccaga ag

#taaatttt  88080

aactataaat tttattataa gaaagggttt tatcattcta tatagatcaa ga

#ggcccagg  88140

agtattttaa aagtgaattt gttattaatg ttattacagc ttacaaacaa ta

#ttattgta  88200

tgggtaagtt tatagagtta cacttaagta gttaagaaac aatatgattt tt

#tagtaatg  88260

tacgaagact tttcaggatt ttgtacttga gtataatttt tggagattac at

#ttaattca  88320

gtttatttat ttgttctttt gaggcaggat ctcactctat cagccaggct ag

#agtgcagt  88380

ggcgttatca tggctcactc cagcctcgat ctcctgggct caagcaatcc tg

#ccatctta  88440

gccttctgag cagctggggc tacaggcatt cacctctaca cctggttaac at

#tttttatt  88500

tcttgcagag acgtcatctc actgttaccc atcgcctcac tgttacaaca tt

#ttagaatc  88560

aattgtataa acagggatga cagaaagtac catagttcta gaaaccttaa tt

#gaggacat  88620

tttccataga gaaaaacctg tatttcctta aatagcatta caccctttta aa

#actctagg  88680

ttttctttac caccaaatag actagaaagt aaatttccaa tttaacaaag tt

#cttcagtc  88740

aaaataacac cagcatacat gctattatat agtctccctt ccttttgctc tt

#tttatctg  88800

aaatccacag catatgtcag tagattataa tttaattaga agatttaata aa

#agttgtat  88860

ccactcccct gatgccactt ccttatggaa agtttcatta tagcccttcc ac

#agaatagt  88920

atgtttgagt cttattcaca aaggaaaacc atctattttt atctagcaca gt

#aggcaata  88980

aagaaaacaa attggaataa tataaaagaa aaagtgagaa caaagaacat tt

#tgcaactt  89040

aagattggct ccagacatgg atgaaaatta aatgttaaat cagttgtttc tg

#ctataagc  89100

attagcataa gatctttgaa ctgaaaagga ctataaattc aattcaaatt ac

#tatattat  89160

ggtgggaaat gggcacagac tctggagaaa aacaaaattt taaaaaaaac tt

#agagttgg  89220

atcctggctt gacaaggtca ctggctaggt gatctttgga aaattattta at

#gtgtttaa  89280

tttgtctcat cattttacct gtgagaaaac tgacccagag aagttaaaag ac

#tttccttt  89340

tattacatgg tggtttagct gtatagaaaa aatataaatg tctttttatt ct

#caactagt  89400

tgaagacact ttatgtaata ctattccatt aaaatgtctg ccaagaggtt gt

#tcctttgt  89460

gatattgaaa tcataatgtg actatggcct tattctcata tctgacaaga aa

#tagtaatt  89520

tatatttatt aaaatcatat ttactttcac cattaattct gattaggatt tt

#tatgctga  89580

tatgattaac gaaaatggtg atctatgtca gttgggatag gctaaattat gc

#tataaaaa  89640

ataccctgca atctcagtgg cttaaaccca tttatttatg gctcacaatt ca

#tgtccatc  89700

atgaatcatt ggggttttgc tcatctgttc attgtattaa atagtgactt ag

#aaacctca  89760

gctgatagat cagtcttcac cttgaacttt gcttgttgca tgtcaaggaa ag

#gatgagct  89820

ccagaggata tcctcttgcc aattaaatac tccagtctga aagtgacaca ca

#cataattt  89880

ctgttcccac ctcatttcca gatttaatca cagacacatg gactcaccca at

#taaaaggg  89940

agccaggtag tgatgttcta cactttccta ggaagagagg gagaaccagt ta

#tgacatga  90000

tatgaccatc acatgatcta tgaggtatta tggccctgtt taggactgaa aa

#actttagg  90060

aataactaat atgaaaactt tctgtgtaga caaaaatgtt ctataaaatt cc

#cagccttg  90120

aagagatata ctgttggtga tttgtggctt aaatgtaagt tttttcaata tg

#gcatatct  90180

attcttacct gattgtaaat tttggcaggt ataagtattc ttttctattg gc

#ttcctttt  90240

cactttctga catttttttt tctttttgct tcctaaacac taaaaacaga tc

#catagctt  90300

tcctgatctc tcttactact ctgcacatta atcattctga ctgtctcttt tg

#gttagtta  90360

cttttggcta atccacttga ttccctaact agttactccc acatatttgt tg

#tgtgttga  90420

aggtggatca ttttattaca caaaatagta agataatata atatagagga tt

#tgaatgat  90480

attgcttgga gagagaaatt ggggtcaaaa atgactaagg agaaaaggaa tg

#agggaaat  90540

ggtggagatg gaggtaggca agaagattta ggctaaggtt cattagaaat gg

#tgaaacta  90600

aattggtcat ctattaggat tagagaccaa attcctaaac ggataagaat ta

#agtggctt  90660

gtgccagagc aataaaatca ctggtttctc tttatctgtt ccatttatct tg

#cttataga  90720

caatctaggt attactattc atttcagtcc aagaagacag tggtccccca tt

#tgacatca  90780

tgacatcaag gttcttctct gattatccat cctggcagaa acacccaggg at

#ggggtctg  90840

agctcaattc tcacatattc agtccctagg aagtgactgc tatcactagc tt

#tcatccaa  90900

gcaagcctaa caaggatttt tcctatgcaa caggccccta attatgctag cc

#tccctcaa  90960

gatcttataa gaaaattacc aagagactaa aatattcagg tttaagacct cc

#cactaagg  91020

aaaaataagt attctttcat tttctttttc aattaccatt aactttccat ga

#agtataca  91080

ctctttatta gtgctacata agattttctc tgaccactgg ttaaacaatt at

#atttaaat  91140

atttcttcag agttagacaa gttaacaaaa taacatgagt tttccttttt tt

#caattatt  91200

ttttaattgc aaaaagaata tgagttaaat ggaattaaaa tgaaataagc ca

#aatggctt  91260

agactagctt ttatatactt ccaaaaccta tgaaccaaga cacaatatga ct

#atttttct  91320

atttcaacct tttatttttg gtataaagga tcattaacct acaatataat at

#aaactgtg  91380

ctgataatat ttgtttgtat aggtggttga agtttgaaga agatgtggaa ga

#tggaggag  91440

aaaggtggag caagccttat gtggctactc tttcattgca cagcttgttt ga

#attgagaa  91500

gttgtattct gaatggaact gtgttgctgg acatgcatgc caacacttta ga

#agaaattg  91560

caggtatatc ttttccccct tagtgtattt tataggtaca gctaattttt tg

#ttactctc  91620

ttttccttat aattcaatat acgtatgaac tttggaaaac taattctcat aa

#tcactgca  91680

taaggtctta aaagtcattt tcttttaccc tgttatttga gataaaagaa gt

#tgaatctc  91740

agagaaatat gctctagttt ggcagtgcca agtctaggac aagaacctag at

#atcttgat  91800

tcccattcac catttatttt cattatcata tttagactct caccattaga aa

#attaaagg  91860

aaaaaacctt agagctagat acttattttc aatattcaaa catatgaaat aa

#ccaaatga  91920

aaaaatttca atatacagaa aaatgttggt ttagaatgga cacagaaagg ta

#cggccatt  91980

cattttaaac ttaattaaaa cccttgaatt ccagaggaag ccaagtgata ca

#gttaggat  92040

tcgttttgta attcaatact ataaactgat gaatgattag tattataatt ca

#atgatatc  92100

ttataataca gacaggtata tttaggaaat gttattatta cagaaattga gt

#caaagaac  92160

tcctgtatct tttgaccaga aggcaaacat attttagtaa aaacaaaata at

#acaaaaag  92220

acagaaatga attttgaaag agtataaatg aaataattga tggaggtttt aa

#aaacacaa  92280

acaaagaaaa gaggcagttg aaaagttatt agtttgggaa aaaataaaat tc

#attccata  92340

tgatttgtat ttgtgaagtg aaaaaactta atatcttaat catattgtag ag

#atgaaaaa  92400

ctatatgtgt gtttttaatc atgtatatga aaataatata ttagaaaaat aa

#catatcta  92460

ctttaatctg cagaacagcc ccatgaagta gatgtcattc tcattttcca at

#cacaaaat  92520

agaaactcta aaattgtcat ggcctagatt tcacccaagg gcccctgact tt

#aagcctag  92580

tgttttttct attacactac aactgctgtc tgaagaaaaa gaaatgtctt ga

#agtgaatg  92640

tcacccaaat tttgatggca catttatcac cttaaaaatt attgatttag tc

#attggtgc  92700

tgataggcac tgcagtatgt gtgaaaagaa aagtaagtac tgaaagatac tt

#tggcttga  92760

aatattaagc aaaaactcca aaaatactaa aacacacaca cacacacaca ca

#cacacaca  92820

cacacacaca cacaccacac tgccccaaat aggaaagata agcggtcctc tt

#ctgtttca  92880

tgtaacacct ataaagagat tattctttaa gttacatagc tagagcctga aa

#gactttat  92940

aaagttaaac ataaatgtat aattttcaga aatatccagg ctactgtagc tg

#cactaaat  93000

caagagaaaa tagagaaaat gattaactca gaaataagca aactccctaa ga

#atgctgaa  93060

atagttagct atccagctca atttcttagc tttacattat atggtcttgc ta

#atacccaa  93120

taaacatttt tatattttaa ttaggaatga aacagcaggc ttttcacagt ac

#tttcaagt  93180

atgggaagct cttaagtttg taattatctt tttaatgctc aaacctggtt ct

#tagtatta  93240

ttattgttat ccttatttaa taaagaaaaa aactaagatt taaaaggtta aa

#ggccttgc  93300

tctaaggcgt ttatttctgc cgcttaaatc gatgatggcg ctacctttaa aa

#atagatta  93360

atccaaatac attttgaaat gggaaacaaa actgtcacat tctaccacct gg

#caaaatta  93420

gcctcagaac atacccttta tacttttacc agtcttcaca tttcttaaat ta

#tgtaattt  93480

ctaatgcttt cctcagaaag ttattcctat gaagaaattt tctcccagta at

#ttgactaa  93540

aacacttcat tttatcactt tagttcactt tcattgtcca aaattatgca aa

#tttttcct  93600

aactctgtcc ctgtttccca agctcaattc tgtagaatat gtgaaggtta ac

#tgggttaa  93660

atctagcctt ttcaagcaaa ttacattctc taagtctacc cttacagtga aa

#gtagttca  93720

gttgacgtct tgatacccta aatagctttt tagtattctt tctgctcttc ta

#attagtgt  93780

gtatctttct gactttgaag tagcccaacc tgaatgtccc atttttcagt gt

#agaacagc  93840

ctgtaaaatg acatttagaa tgtgtcagtg gtttaatgct aacatcacaa ag

#aaaaatat  93900

gattacaaat atttgtgttg atcattatta ctttagattc ctttactgtc at

#tactaaga  93960

agagatttcc tctcattgaa aactataatt tggctaaatt taaaagttac tt

#atttatcc  94020

cctcaatata aactcattaa aatattttct ctctatagtt tgtaattatt tt

#cttatttt  94080

ttacttctcc tattttcatt ttataaaaat tgaggggcat tactaagttt gt

#aataaata  94140

agcatgcttt ccgtttttaa gacttctaac tttgcaaagt atttccacat aa

#ttatgttt  94200

tattatcata acaacatata aagtaggaaa gagactattt caccataaac ag

#ataaatag  94260

aaagttcttt atcaaagatg acctttgcag aaataaaaat aattttttta tt

#aacctata  94320

atcataatat ttggggatgg gatctcctat gttgcccagg ctggtcttga ac

#tcctgggt  94380

tcaattgatc cacctgcctc agcttcccaa agtgctagga ttacaggcat ga

#gtcactgt  94440

gcccaaccat aatttttgtt ttattctgtt tcatgatcat ttgtggccat ag

#tgattaac  94500

aatcagccct gaaacttttt cctcagctct tatttaccat gatttttctc tg

#ttagccat  94560

aattcacata cattagtcac tagtttcagt tttacaaacg ctaagtgtaa ga

#gcttacct  94620

ttaagggttc taatccctag tactttgtga atacacaggc tttacagtat tg

#atgttttt  94680

cagacatttc ctactagatg aatatgaccc agatattgtt ttgtaatgat ca

#aggatttt  94740

tatatcaatg ttttgatatg tttttaacag actcggataa ttccttaaga ga

#tttttgta  94800

gacttagtag cagaaaatcc catttgtatc tggcagatct gtcaagaatt tc

#tgatataa  94860

ttaaagtagg attttctttt ggctaagtta atttaaaata tatctgtttc cc

#aatgtttc  94920

aggaaactca ataaatttaa actttatcct tcaaaatatt acttaacctt tt

#caaatcca  94980

aaattctcca gatatatctt cttaccacaa tttactctga tatggagatt aa

#ttgtattg  95040

aatatgcttc tgaattatat tcatataaat tacagggaat tttatggtct at

#gttaatct  95100

ctttgaaatt aagcattata aagattaatg atggaaatat cctctctgca gt

#gtgtgtat  95160

actttaacct aattctgtca atgagagtta ggaagaaatt aaaaccaaac ca

#aagttggt  95220

accatggaca gattatcaat catagctccc aactcattta aacaaccttt gt

#tgtttaaa  95280

atctttcatt gaaggaagaa tctacagttt gctccactga atgtaatctg ta

#gagttggg  95340

agtataggaa taaccatata ttttttaacc tgcctatact gtgacaatcc tt

#ggtctgaa  95400

aagtaagtat tctattacag tttacatctt tagtacacac atccctgtta gt

#gctggcaa  95460

ccaaaccaca gaatttagga acttcgtatc atattccccc ccacctctcc ca

#atatcttt  95520

taaagttaag acaatgggtt ttcaaagcat tgatatgatg atcttcaaaa ag

#gcagagat  95580

ttatgtagaa tctgcaatat gtcataacct ctaggggctt tcattcaaga ta

#cattatga  95640

taaaatagtt atctgatagg atgaaaaaca atttttcatt tttctgaggc ct

#ttttccac  95700

aagtgctact agtttttctt ttcttttctt ttcttttttt tttttttaga cg

#aagtctcg  95760

ctctgtcgcc aggctggagt gcagtggtgc gatctcagct cactgcagcc tc

#cgcctcct  95820

gggttcaagc aattctccta cttcaatctc ttgagtacct gggactacag gc

#acacggca  95880

acatgcccag ctaatttttt tgtattttag tagagacggg gattcaccac gt

#tggacagg  95940

gtggtctcaa agtgctacta gtttttctag agtctgctta gtgttagcag ag

#tgtgacct  96000

atttgtcctt tttttctttt cttttctttt cttttttttt tttttttttt tt

#tttgaggc  96060

ggagtcttgc tttgtctccc aggctggagt gcagtggcgc aatctcggct ca

#ctgcaagc  96120

tccgcctccc gggttcacgc cattcccctg cctcaacctc ccgagtcgct gg

#gactacag  96180

gcgcccgcca ccacgcccgg ctgatttttt gtatttttag aagtgacggg gt

#ttcaccgt  96240

gttagccagg atggtctcta tcccctgacc tcgtgatccg cccgcctcgg cc

#tcccaaag  96300

tgctgggatt acaggcgtga gccaccgcgc cttttctctt atcacccaga tc

#ctggggca  96360

gaatagactg tattatgtag gcataatagc ttgctgagat tgcaggactt ca

#ctctggac  96420

ccaacgtcat tatggtccgt tattctttca cacttttcaa attaatacta at

#atgtattg  96480

tagtggtgaa aagaacaatg taagtgatta ctaattcaga ttccttttgg ta

#cttaaatg  96540

tcaccctagt ataaattata ttcttaagca aaatgagtaa ttttttccag ac

#aagtagat  96600

ataatttgat acagttatac tttggagaag tttgctgtgt atttctctgt aa

#ctaatgaa  96660

cagatgagtg tgttttttaa tatttacttt tctttacata actgtttcaa at

#aaaaatct  96720

tatctttgaa aaactgtgaa gatagtgacc tatggctttt ttagtgttcg ag

#cctggaaa  96780

cattgtgctt taatagaaat taaaaataat aaacatatgt agggtttatt at

#gtgattac  96840

ttttgattct gactagaata ttgaactggg aattcatatc atggcttata tt

#tggaactg  96900

ctttacaata atatcatatt gatattctaa taacctactt tacaacttcc at

#tatgaagt  96960

atatgcatat tttatataca tttttccatc ttagcaaggt ttcagtgtaa tg

#tcatatac  97020

gttgacaatt tattatttcc tttatttcag attaacccag gggtattata ac

#tactgatc  97080

tccaaagaac tgaaaaatag atttaaatat tattctatag tatcacacat tt

#tcagaatt  97140

ggaagggacc tttgaggtaa ttatagtgac tgactttcaa acattccagg ta

#tataatat  97200

gggtaacttc caaatattct ttctacctct ttccattgta aacacaaaaa tg

#atagagca  97260

cactatatcc cacgtgccac atatggccga ctgcctgatt ttgtagggca tt

#tgagctaa  97320

gaatggtgat tatattttaa atggttgaaa aataataaaa aagaagttaa ta

#tgttgtga  97380

tgtgaatatt atatgaaatt caagtttcag catccttaaa aaagtttcat tg

#gagcataa  97440

ccaggctcat ttgtgtacat gttgcctgtg gctgctttct tgctacaaag gc

#aaaattca  97500

gtatttgtga cagagatcat atggcctaca atgcctaaaa tatttgttat ct

#ggctctgg  97560

acaaaaagag cttgtctttc tctggtttag agaattaact ctagagtgaa gc

#gcagttct  97620

tgattagcct gtcagtcata tgaataccat ctcctttgcc agtgattggt tc

#aagatggg  97680

cagggctatg tcagttagac ttaggataat ttttcctggc caggtgaaaa at

#aactcatc  97740

taagagaaag tcacaaaaaa acaatatatt tctcactgga tatgaacaaa aa

#tatatatt  97800

tccttgttgc tgctggaagc caccttatga ccataaggaa aatcagcctg ag

#gttaaagc  97860

ttaccctaga ggaggaggaa gttaacaaaa tcacagagaa gcagaattat ag

#ccaaccta  97920

actttgatct ttctatttat gtgagccaat aaaattgttt tatgtagttt aa

#tttgggtt  97980

ttctgctatt gataagccca gctttgtctc tacttgataa gctgtcacaa aa

#tatgaaca  98040

tattgaaacc accacaaatt tcaaaccagg aacccataat ctacattatg aa

#aattacaa  98100

agaaaatctt gttctgggaa atatttactg atagcctcaa tattccaatc ag

#tgcatcag  98160

gtgccttatg tcattagtct tggcaccaat atatgatata gatattatta tc

#tccatttt  98220

acaaataagg acacttaggt tattcaactt tgcaaagttg tctagctaga at

#gtcataaa  98280

gtggcccaaa tctgtctcct agttcatttc catttcacac tgaaggaaaa ca

#ttgttggt  98340

aagggagcat tctgctaact ttgaaacctt tattgtactc aaaaaggcag tg

#gaaggcag  98400

ctcattgtaa tctgctttac ataagatgtt aatgcctaaa aaacaattag ag

#ttaatgtt  98460

tgataatcag aaagcagatt aattacacaa acatccattg atgtgatctt ta

#tatcacta  98520

agaaacttaa aataccttta cttatctatt ttactgacat ttttgatact at

#gtatggta  98580

aataatctgc ttaattatag acttctgaaa tctcaccttc cagtctttgt tt

#tgcaggta  98640

tagaatatct ttttaatcta acattctcaa gggagtgtgt ttccagcaaa gt

#ttgagaaa  98700

gggctgattt tctatccata tgaaacagaa ttgtttactc tccaaattca gt

#aactatat  98760

cacttcatag gcctctttgc atcagatttt cacagataga cttttgttca ct

#taatgggg  98820

aaacaaggaa attagtctgt actagaaaat gggaaaaaaa ttaaaatata ag

#tataaaac  98880

caattttcaa attcaaacac gttatgaatt gtgaattcaa acacattatg aa

#ttttcaaa  98940

ttcaaacaca ttatgaattt tgatattatc tctacagcta ttcctcccat ca

#gtgtggat  99000

aataaataaa taaagaactt tcttctcaat gcaactattc ccatttgaaa aa

#taatactt  99060

cataagaatt atatatttaa atagaatggt ttataatgaa aatttgccca aa

#tctttctt  99120

attcaacatt tctacaatgg aagataaatt tccatttata acagcatgct ta

#gagatttt  99180

ttaaagaagt tatttctatt tcaagatgaa taatattgtt tagggcttgc at

#atttggac  99240

tcagtggttc acggctggca cacgttctag aggaaagctg tgcttatctt ct

#tccggcct  99300

tttctcttca gatatggttc ttgaccaaca agtgagctca ggtcagctga at

#gaagatgt  99360

acgccatagg gtccatgagg cattgatgaa acagcatcat catcagaatc ag

#aaaaaact  99420

caccaacagg attcccattg ttcgttcctt tgctgatatt ggcaagaaac ag

#tcagaacc  99480

aaattccatg gacaaaaatg gtaaatgttt atttattgtg ctctttatgt ct

#actatagg  99540

tctctgacat atcaaagcgc ttctaaatct tttaaaactt gttttatttg aa

#aatgattt  99600

tttgaaattc agattattgt agaattcttt tcacatgagt atatattctt at

#tatcaagc  99660

atcaagttgt aaaaatttta gaaaagaact taagtttcct gaaaggttca gg

#aaaaaaat  99720

gcaaagaaaa ctaatattta ataaaaaaac ttttagattt ggctgcagaa aa

#cataaaca  99780

gagcatctgt ggcataccaa ataaggtcct agtctctgtc ctgtagctta aa

#aatgtaat  99840

gcagggcttt gacttacgcc atagatggtc ttttagttta aaggaatcat ga

#tcatcatc  99900

tagtgtttgt ggaaaaaaga tattggtttc atgttgctca tagtcaacaa at

#tccattag  99960

agaaaatgat tgaaaagacc agccagtgca ttgtttgtgg ctttacatac at

#tatggctg 100020

attccggttc aagggctcat tgctgtttgt aatgcagcat cttcaacatc ca

#tggagcca 100080

ccccacttac tatcttcata aaccaacata gatgaccacc attgtttcct ag

#caatcaac 100140

ttactatgat ttatgcttca gactattttg tctttcctgt attttttgtt ct

#ctccttgc 100200

gtttatttaa cccctcatca tttgcaataa ggaagttgct taggaatctc ct

#gttatcat 100260

ccatcctttc tattagtctc atgagagaaa atgaagttac catgaagatg at

#atgaattt 100320

gttaaacttc tgtaggcttt aaaagtttcc agttctaggc cgggcgcagt gg

#ctcactcc 100380

tgtaatccca gcactttggg aggccgaggc gggcggatca agaggtcagg ag

#atcgtgac 100440

catcctggct aacacggtga aaccccgtct ctactaaaaa tacagaaaaa tt

#agccgggc 100500

gtggtagtgg gtgcctgtag tcccagctac tcgggagact gaggcaggag aa

#tggtgtga 100560

acctgggtgg cggagattgc agtgagccga gatcgcgcca ctgcactcca gc

#ctgggcta 100620

cacagctaga ctctgtctca aaaaaaaaaa gtttccagtt ctaaaagata aa

#aattaatg 100680

aaaagtattt tcaaatgctt tactggaaag actgatttcc acgaatggat ga

#aagcacat 100740

gtaatgacag cgtgaaatat catgtaatct cacccttatt ttcaaaagct tc

#agagatgc 100800

cttaaataaa atgtatgaaa attagttttc ttcagatttg cttcatatta at

#cagttttc 100860

atgctactgt atcaaatata cataaaaata tagggtaaat gctttattaa at

#agataaag 100920

atgattagat gtaattttgt ctcagaatgt agaaccagtt cttaatgaca aa

#atcatttt 100980

tgagatagtt gatttttagg gcttttcaat gactgaatat aagtcatttt tg

#ttacatac 101040

aagagtctat agatgtgcac acttaagttc aataaaatta ttatgaatac tt

#tatggtga 101100

ataccaactt gtgtttgtag attccactga acattctgag gagatataac tt

#gctttgaa 101160

tcaaatcata tatttaaaac atatttatat tctaaatcac aatttgcttt aa

#aatatgtg 101220

atacataaga taacaaaact tgaggctttt atattctaag agatgtatta ca

#aatgcagt 101280

gcttttgtta tgcttataat gctagtattt atttggtatg gtagtgttaa aa

#tagactca 101340

gttatttact aattttggct atgggattat gtctacatga ttccaaaaac tt

#tattagaa 101400

ttaacttcct aagaatgcat gcagatttta taaaaatgaa cttttacctt ca

#taactttt 101460

gctagaaatc agataagata tatgtcttta agaaagaggt atgtttcttc aa

#agaggcaa 101520

ggatcttgca ttttgaacta gttaaaattt ataccttaaa tttcattgga ga

#taatgttt 101580

actataacaa taatttcatt gcattttttt ttcaggcaag agactacaga at

#ttattgga 101640

gcaatgattt attgtaatat gcagatctag gcacactgtt tgttactgct tt

#aaacttct 101700

attaaacatt agaagagatg ttagaattat aactgtgaat cacaaatcta ca

#tatagtca 101760

caaggttttc tgagagcctg ctttttgtct tatttaggaa atggtttagt tt

#tcccaaaa 101820

atcagaatct gagtggttct aaagtgattc tgtcaccatc tgtacaatca gc

#ctttatct 101880

gaacacatac aaatcttttc gaggcatacg taagggcaat aaaaacttgg aa

#acatttct 101940

aataagattc atatacccaa ttaagtattg ttgtagagta tgctgtcaga ag

#tggttttc 102000

taagcctaag cttataacac ctccttatga ctctgttttg cttcctcaca ca

#ctttgcat 102060

aattatgtgt gttgagaatt ctgaaaatat gtatagactt caccaattta ga

#agtaaatc 102120

tcctacccaa aagtgaaaaa aagtacaaaa gacctttact gctaaggttc tt

#aatctact 102180

tatgaactct aaagcctgac aaactctaga tatataaaca aattgaaatt aa

#tagccgta 102240

aatgtaaatt ggaaattctg ttttaaatat gcaatcaaga tttaaatttt tg

#tgcaatag 102300

ttcagagaga tgcaaaagga tttcaaaaca tcaaaaaagt aaaggtaata ct

#attaattt 102360

ttaaaaatct ccttagtaaa atccattatg caaaaagatt gactttttta aa

#aaaaaaga 102420

ttatagaata gaaattaaat agagcaaaga tttttccaga aactttaaaa ca

#gaacacat 102480

tttcctccct aagcatagtg gtagaaataa gtccccgttt cttgtttaat gt

#gctaaaat 102540

tatctcaaaa aggggatcct ctagagtcga nnnnnnnnnn nnnnnnnnnn nn

#nnnnnnnn 102600

nnnnnnnnnn nnnnnnnnnn tcccggaagc agagcgggag aaagaaggcc cc

#gtttcggg 102660

gtgaatgtgc gaaaaggagc gcaaaaacaa agtgaagctg atgtagataa ac

#ctgaaaga 102720

gtcagataga agaaagttag tacgtcctga agtgacttgt gtcttgagca tg

#ttaccttg 102780

tgagtactct ccggggttaa acattcagac actgtatttc aaacggggtc tt

#ccccattt 102840

taaagattag attaataaaa tagtgcattt ccttgctctt ctccttccca ag

#tctaccat 102900

tctttgtcca ttcctttttt agtgatttgt gataatttgt caatctcatc tc

#taaacaca 102960

ctagttcact cgtttgaata atttttttct tcgtattccg cattctcttc ag

#ggctaatg 103020

tgaaggatgc tatggattca ccatgcattt ttaatgccac catgctgtgt tt

#aactttca 103080

cttttcatta agcatcaaaa ctgtgagaat taaatgtctg attctgatgt tt

#caataaaa 103140

agtgacagtt acatttggca aaacaacagc aaaaataata gaaaaataat at

#ctactttg 103200

acattagtac cctgaaaagg gtatgggtgg taaagcactc aaaataaatg ta

#tcgaaaat 103260

attaaaataa ttatttgaat taggaagatt ttctaaaact aaaaataaaa ct

#tttaaggg 103320

atctagaaga caaattttat cagtatctgt atttatcatt taggtcatgt at

#tcaattac 103380

cttttgagac attgggatta taaatctatt ataaaatatt attatcctta tg

#ataatttt 103440

tatatttttg aagataattt gggattatta gttttcttaa gtataggatg tc

#tttattct 103500

gctctatcct ttactaataa tttctaactc tgttcgtttt ccttcacata tc

#ttttgtct 103560

ctcctaatct gaatactttc cagttgtacc ttttatttag gatctcaaaa gg

#agttacag 103620

tgcagaaagt ctctaactac tgttcaacgc cataagttac tgaaaagcag tt

#agatttgg 103680

gagcctggga cataaagttc actctttagg cctgggtaga tttcagccct ta

#aagcaatg 103740

tacacatatg tattgtgcat aatatttatt tatggttttg gaaatcagac ct

#attacatt 103800

gtagttactt cttttacaaa tgctgtactt ttaattttca gatgcatgct gt

#ctttacgt 103860

atttagatat atatgctttc ttgctttttt aatacaatgg tctcataaat aa

#gatatcca 103920

ggatttaaaa tttatccctc ataatgttct acctttgaag aaaaaataaa gc

#tagaataa 103980

taattcttga gattgcttga aagaaaactt attaaaagat ttgtgtatat ta

#aataatta 104040

aacattgttt aataaatatg atattttcca ccgctccaag aaaatcaaga tg

#acattgtt 104100

gacacaactg atgggcctgc ccagaggcta tattgtcatt acagttttgg aa

#tgtcaaga 104160

ctagatttta agagcaaaca taattctagt atgaagtgtt tgaatttgtt at

#ttcttata 104220

ttgcattaat tattttcagg catactaatt tttctccgag tttaattgtt tg

#catacttc 104280

tcatgttttt gaagtgtagc tcacctaatc agcattttct aaatatttag cc

#cttctttc 104340

ttcatgtttt ctattcccat gaataaatgt attgttacac atgtatgtaa ct

#ttgtcatt 104400

catctttata tttctttatt ttgctctgtc ttgtgtctgt ctctaacagg ct

#catctcat 104460

ctctgtacct ccctcatctc ctaccctttg ggtactctaa atgcgttgaa gg

#tttctgag 104520

gtagtgtaaa ccagcttggt ctctaggtta atagtaatgt acctccatgt ct

#tcatccca 104580

gtttccttct agtgcacgtg atttacagtg gattaagcag tagaaaataa tg

#atacattt 104640

atgcaatata ttctattgat acgaatttgg ccaactataa atttaaaagt tg

#ctaagctg 104700

ctgttttata atacatatgt gcatacttaa agaagaagag aactatagct aa

#agacaaat 104760

gagttaatat aatactcaac agggtttttg agaatatacc tttttttcca at

#aatgaagt 104820

gttttaaaat actgctatta attaaagtca tgaaatagta cttttgatgt aa

#tctcatgt 104880

tccttccttt atgataaaga aactgtatga taaagaaaat gactttacca gt

#ctcacaat 104940

acacttagtg aaaaatttat ggtgtaacaa gcagaaaaac agcttcattt tt

#ctagttag 105000

tatttactca aaatactctc agttttctcc tatgctagcc ccatatctat ta

#taatttgc 105060

cctagaaaaa ttcatggtct ataataactt tttatctgac acatatgatc cc

#tacatgaa 105120

gactcaaaga aaaaaaaatg aatttgtaac tcaaagaaaa gtaattcaaa ca

#ggtgctaa 105180

tatgaatact atataatata tatcttaatt ggtaagatat caaacaaata tt

#agaaattt 105240

tgatttaagg tgaagaactg ttgagcttaa caagtcataa aaatgtattt ag

#taaatagc 105300

agaggagata ttaggtttct caaatgtttc catttacgtt taaatagtca ca

#gataccag 105360

ttaaccttag tgatatctac ttttcatcag ttttttaata acttaccatg aa

#tataatag 105420

attactcaat gtcttttttt catagtcatc ctcatgcctc aaaattttct ag

#gtattata 105480

aaaacagaaa taattgaaca ttgcaatgac attcatttat aggaaataat at

#gggtagtg 105540

atcagtggac aaaggtaata taaagaaaca ggtaaaaagc atttgtttgt aa

#gtactgtg 105600

gtatagcact ttaaaaaaat tacagtatac aattagcatt cataaagctt cc

#acacatat 105660

atgagtgcta aatcctaaac ttatactaat ttttttccgt gagggaaaaa ta

#tcctagca 105720

aattctttgt tattctatta ggaaaatttt tacttctggc tgaaggtaaa at

#tctgtacc 105780

tgaaaattgc cattctgtga accattattg ccttagacat cagcaagaaa at

#aagagatg 105840

cccttccaaa atctgaattt attgattctt cttatgtaat agtatttcag tt

#aatgaaat 105900

taattttgaa atttaatcca tcatcttctt ttgaaagatg gtaataattg gc

#ataaacta 105960

aataattggc atagagaaaa atatatttaa acaatgatta caattgataa ta

#gaactata 106020

aaatcatttt taatttatga ggtttcaatt agttctatat actataattc at

#gcttgaat 106080

attggtttta tatatacagc aaataaaatg ttaagctttt taaaagactt ct

#attttttc 106140

aaaataaccc aaatcaaact tgttagctta atttttaaat agtatctata ca

#tcgttcta 106200

tatactacca agttgtgaaa actgccttga ggatatacac atttaatgta ca

#ttgtttca 106260

actttaacaa attaacttac atttttagaa ataatagaca agaaataaca ag

#atttgaag 106320

tgctacttaa acttcgcagg acttttgatg tgattaaata tatttaatta tg

#aatattaa 106380

cgcctatcat ttaactactg ctctgaaata taaacgatat acaatttgtg gt

#ctttatgt 106440

ctatgtcata ggctagtagt ttttatggct ttttatatta gcatacattc ta

#tacacata 106500

cctagaatct aggactagca agaagtttac tgtcatctga tgtgtctgct gc

#tagttaaa 106560

ctctcaacta ggtcattatc aacatcactt aaaatattta taaaaatagt tt

#ctaaatcc 106620

cttcttcatt atcaacctta taaagtaata ttttctaaaa ttgttcttgt tt

#tagaacaa 106680

gaatagcata caacaatctc aaaatatatt attataatta ttacataaaa ta

#ttaattat 106740

taattactgt aattatttac aaggagaaat acaagtatta atattttaaa ca

#tactacct 106800

gagctgaagg taatttatga aatgctctgc ttaaagtata caaatgaaaa ca

#taaggtat 106860

tcaatttctt caaatgttaa gttccgcata ttttctatcc aattcaaaat tt

#aatctctt 106920

caaagttaat gactttgcac tgggttgact tttgttttgt atgtgtttgg tg

#atagaact 106980

aaataattgt tcttccatgt agatttatac cacacgaaat gaattattat aa

#gaaagcag 107040

atatgtgttt atttaattta tccatgactt gagtttcacc actcaatttt ac

#agaacatt 107100

caataaattt agttttaaat atatctaatg ttctaactca ttaaaatatg ga

#gaaatgat 107160

gtgaaactgg tgattgaaga catctgttgg tagcacaaat gcattatgta aa

#agattttt 107220

ttaaaactac agttattatt ttgagaatgg taaattgaat ggctgctaat ga

#acagttca 107280

cagtcatagc tgcacattgt ggttagaaat gggagaatga gaataattta tg

#tagcttgt 107340

gtgacattta tctgaagttt atatatttcc ctagaatatg ctatactcag aa

#tttgtgaa 107400

catggtttga ggtgaactta ttttaaaaag tcattttatt ttcatcttct cc

#aaatatat 107460

tcttttacat tttttaatga aagtagtgaa atccttaagt tctagaagaa ta

#ttaagcct 107520

attactttct ggcattataa caactttaaa ccataaaatt actcctatta at

#aaatgacc 107580

cctgcttgag aggcttacta gtccaaaaag caaacttata gtaatatttg aa

#agtaaata 107640

attagtattt ttaaccacag ttggtaattt ctaggtaaca aagaataagt gg

#gttttcag 107700

gagagaattt aagggaaagc gtttttgtgg ggtttttttg catttacact gg

#gagtttag 107760

agaatttcag tcagagactg aagtgattag agatgacact aaaggtgaat tt

#agaataaa 107820

attgggattt aggtaggtag agagaagagc cagacagaga gagtatttct aa

#catctaca 107880

actgacgtga ataaaagcag tattttgagt cattgagtta ttatcataaa ta

#tgagcaag 107940

gcttcagagt tgagttgtct ttattcattt cacagaaaaa aaaaagatgg gg

#agatgttt 108000

aattttcatt gcattgctaa ctatgaacaa atttcatatg acttactgca aa

#caatgttt 108060

catatttagt gaatgatgga atttaacctt ttctagccat tgccacactc cc

#agagctac 108120

tatccactta attctcatca tcttccctat aatagggaaa agaactacaa ga

#taattttg 108180

ttttaattta ctgttaatgc aaaactaata caattcaagt ttttatcttt tc

#tcacatca 108240

cagactagta ccagtatgct tatataatag aatagtcaga ggcataaaat ca

#tatccata 108300

gtgttcatac tgtgtgaaat aaaggtattt ctaactgaac ccccttatat ag

#aaaactgt 108360

aagagttatg gccaaagaaa tttttttcat tggtttggct ttttagatgc aa

#tagaacct 108420

aaaaatatac tgtgtaattt tcagataaat atccgtcctt tttaatgctt ta

#cattttaa 108480

attcttcagg ctgagcttac atcttaacag atgtctatct tgtcttttta ta

#tacgccat 108540

tagttttggt tggaatctag aaatcaatga tgcttcaaaa tcctggtaac at

#ttacatat 108600

tttgtagata atccttattg aaaataatct tttagagttt ttatctgaaa at

#atgtttat 108660

tttttactga attctcccat ttctacctgt tactgataat aagaatgttt gt

#attaatat 108720

agatttattt atattgaccc ttcattctta catcataaat ttattaagaa ac

#ctgttagt 108780

ctagtttaat tgaagtgcct atttcactca gtatgtctac aactatgtaa gt

#aattgttt 108840

gtattctgtc acaacaatct cttttagcag gtcaggttgt ttctcctcag tc

#tgctccag 108900

cctgtgttga aaataaaaat gatgttagca gagaaaacag cactgttgac tt

#tagcaagg 108960

tgagcttttc tccctctcat ctaagtaagt tgctaaatta ctactagaaa tt

#actaccca 109020

ttttaagagg tgttgacaca atattttgca tgcgcttttt gtttcttgtc aa

#agcttgat 109080

attgttacag aaaatgttag cattaagtcc acatgtaaca ttttgcctat tc

#aaaaaaaa 109140

aaaaaaaact gaacctgtga gttttatgca tagtattcat gtttcagcca ct

#tggtataa 109200

tgttatctct tccaataaaa agaataactg ggcttcacag ggaatttaac ag

#aagtttaa 109260

tctatttttg tttgtttgtg tttgttgttc tttgtttgtt tgtttgaggc ag

#agtctcgc 109320

tctgtcaccc aggctggaat gcagtggtgc aatcttggct cactgcaacc tc

#cgcctcct 109380

gggttcaagc aattctcaag cctcagcttc ccgagtagct gggattacag gc

#gtgcacca 109440

ctatgtctga ctaatttttg tatttttagt agagacgggg tttcaccatc tt

#ggacaggc 109500

tggtctcgaa ctcctgacct caggtgatcc gtccgcctca gcctctcaaa gt

#gctgggat 109560

tacaggcgtg agccaccccg cccggccaag tttaatctat tgtttaaaaa ct

#ttggctag 109620

tttgtgttca aaatcacttt tcttctattt gtgggaaagc aaatcataat at

#aaaactga 109680

attgttaatg taattaagga aaagtcatta ctgtaaggaa atcctagaag ga

#cacagcaa 109740

aactgagcag agttttaaat aaaaacatat taagaactga ctgtgttgag gg

#atacatct 109800

aattggagac aactgaagtg aaatcattaa cttgaatgta ttcttagaaa at

#gagtcagt 109860

gacaatgatg tgattttgat tagcaaattc ctgacattgt atatgtgcca tt

#gcaagcta 109920

tggcaaagta acaattgagt ggaaaagagg agtttctagc cgggtgtggt gg

#cgcgtgcc 109980

tgtggttcca gccacttggg aggctgaggt gggaggattg cttgagccta gg

#aggcagag 110040

attgcagtga gctgaggtcg tgtcactgca ctccagcctg ggtgacagag tg

#agaccaca 110100

tctcaaaaaa aaaaaaaaaa aaaaaaaaaa gacaatgcaa aagagaagga gt

#ttgaatac 110160

ttggtgaaaa tacggcaggt taacaattct ctttatctga gtggctgaaa ta

#gaagtaac 110220

tcagagtaat attttaataa agcccttagc actggcaata attatagtag tg

#ggaggagg 110280

tgggaatgga tggaagcagt agaggaagta gcctgaatca aggttctgaa aa

#gattaata 110340

gtgatcagct ccttggacct gtttcagaat ccctctgaca atgcctaaat aa

#tctagatc 110400

tagttacgtg catgctctcc ctctggtgcc tggcggagtc tccgtgggag ca

#tggtgtac 110460

cagcttaagt ctgttaatta tgcgtgcagg gactgggagg ccaacaaaag gg

#gcatacta 110520

gtccatgtgg gatgaaacaa aggcatgaaa aaggacctcc acaccagcaa ga

#gagagagg 110580

tgagggcata ctcgggctct atttctacag tggttcaaag ctcatttcac tg

#tatggagg 110640

catgtgattc aaacattaag ccagttgaaa tgtattccat ctgccactct aa

#gaactatc 110700

tttttaaagc attgcatctt cattcatctg caagttggaa aaagttgtca ca

#aactgcca 110760

tacatttaat ttctgatatt cttaatttga aatgatctta aaagcaataa tg

#taacgagc 110820

tgcatattta tgtataaatg cattaacaac ataaagaagg catatttaac at

#cctcagaa 110880

acaatcatta taaagcacat agctcctcct ttcaaataaa ttgtgattta ac

#tttttaaa 110940

aataatataa cctttataca ctgattgtgt atctccatat catgttgctt tt

#ggttgtgt 111000

gacctgcctt tgcagccttc aagaatactt catcacatat gaaagaaaat ga

#agattgcc 111060

agttgtaggc agtagtctca tcttctggtc ccccctcaaa cagttaaaac ta

#tggaagag 111120

tcaaacttcg atttcctttc ttttaatcct tttctttctc ttcacatttg cg

#atcactgg 111180

cccgtttcat cttttaatag gcaagttaaa tttctagagc cctctactta gt

#gtcagctg 111240

ttgttcatag catggcacac tggaaagtct cttgttcata gcatggcaca ct

#ggaaagaa 111300

tgtggctttt gagaaacagc atgagatctt gaatcccaac tctggcatta ta

#aactagct 111360

gatcttggag aagttctcta aagttcagcc ttctcatttg caaagtaaga aa

#actattta 111420

caatttcgtt gtgaagattt aatgagctaa tatagaggga ggtgctggaa ca

#gtgcttga 111480

cttgtagcag gtatttaata aaaggtggtt acacttatta gtgtggttat ta

#gtagtagt 111540

agagataata gtgtcagaaa tgaaacacca gaccataatt gaatgttttg gt

#ctccactg 111600

ggtctttagt gccttgaata gtatttggta tatatttgtt gaatgaatcc tt

#caagattc 111660

aaaataatgt aagcccagtt ttggaattta aaaaagacta agtaagattt tt

#tactttaa 111720

agtctgagag ggcagaaaag tagagtttga aaagagcaat tgtgatctat ca

#ctatggaa 111780

acaaatttta gtgccagatt ttgcaggtgc atgagttgat attttttagc ct

#tatgattt 111840

tagtttagta gtgaatttat cagaattcac ctagtctcca ggttagttct ct

#gttttaat 111900

attttaagtc ttaatataca gattccaaaa ccccagaatc ttaatatgca ga

#ttccaaac 111960

attttgaggt gttaagaaaa aaaaggtctt tattcatctt atatgatttg at

#catattta 112020

ttccatctac attcaaccta catatttgta acccttccag tggatagacg ta

#tcaaactt 112080

acttaaggaa tgattaggaa aataactgga attatcaggt tttagcttcc ca

#taatactt 112140

ttaaaaagca gatgtgtcaa agcaatattt gtttttgttt ttcaagctga ca

#gtggaacg 112200

taggtatttt atgttggtgg tgttttcttt tacttcaaat gacccagaga tg

#gcttcaca 112260

taattttcta catagaaaga acttccgtct gcatctagct ttagtgtatg aa

#acatatta 112320

gagagagttg tattatttaa tcctagaact gtaggaaacc ttagacatct cc

#tcatttag 112380

tcagcaagaa agctgaatta tagagtgatt aagagagctg ctcaagatca ct

#ggcgagtt 112440

agtgtcaaga caccatttct tcccagagaa tccctatgaa gtttcttgta ct

#ttctataa 112500

ggggctgaag gcttaaattt tctccttaaa tttccatctg tttttccttt aa

#ctcttagc 112560

gtgtagtttg cccagacact tccaatttca ccttggtctt ctatctaatc tc

#attccttg 112620

ttccctagaa atgtaactgt ttctcatcca cagattaagt atcaaaggcc ca

#gaaagaaa 112680

tctttccact accagcataa aggtgaggtc tgggcagccc agaagcatga gt

#gtaaatac 112740

agacccagaa gagtatagct cgatttcttc aagatcctat tcagaggacc ag

#aaacttcc 112800

aggatttcct tcttgtccat tccaagtgtt tgtgttcact tgacagtttt ct

#tagggatg 112860

tagttcaacc tagattctct agagctgctt tacatattta taattttata ag

#aggtcaca 112920

ttcaggtctt taaacataat attttattat attaaaagtt gcttaggggg cc

#aagggcat 112980

ggtggctgac acctgtaatc ccagcatttt gagaggccaa gtcaggagga tc

#acttgagc 113040

ttaggagttc gagatcaacc taggcaacat ggtaagacct catctctaca aa

#atctagaa 113100

aaaatcagcc aggcatggtg gcgcacctgt agtcccagct actcagaagg ct

#gaaatgga 113160

aggatcagga tggcttgagc caggaagttc gaggctgcag tgagctggga tc

#gcaccact 113220

gcactccact ctggatgaca caaggagacc ctgtctcaaa aacttaacca aa

#ccaaaaaa 113280

gatagttggt ttgtcaaata agtttcttca tgaagtatat agtacacaaa ca

#caaaatat 113340

agggttgccc cacgaataat ataatatgta actatacata atataggaat aa

#tataatta 113400

gataatatat aatcgattac ttcccaaagt atatgattac tccaagaata at

#gtaatgta 113460

atgagtataa tacaatggct accccagata tgtgctatag tactataact ta

#ttccattt 113520

gaagtcaaaa gatgaatttg cttatcctga atttaaattc tgtatatttt aa

#tgtttttt 113580

ctaaataaca ggtatcaatg atatattagg tattttgtaa atttaaagat ca

#tatgtaat 113640

gaccatatat tttcttttac aaaatttaac tattttaaca tactatgtac tt

#cttgattt 113700

aattaaattt catctttaaa cagttatttc tataatcacc agttgcccga gg

#cacagact 113760

ttcatagtta agacaatggc atttgtcaag caataaatga gtttatagaa tt

#ttcaaggt 113820

ggaatttaaa tttcaggtat tatcaatata attcatatta tcaattatgg at

#tttaaaaa 113880

aagatgtttt ctcattttaa attttgttca gtatatttat attgtatcat tg

#ttctttcc 113940

attgagagag aaaacttaac tgtttattct tttagtaaca gaaaggatta tg

#agatttat 114000

tatgttttcc tcacagagct gatagtatat gggaaatctt ctattccctc ct

#tgggaatt 114060

ttggcattac aataaaaatg taaagcatta ctaatttaaa gcatcttaaa tg

#tgtacatt 114120

tctcctaact agataaatac ctacaaaaat accacaataa atcccatgaa at

#ttaacctt 114180

acttattata gtaaataaat acttttgcta tctataaact aaaagatcag at

#tccacaaa 114240

agcaaaatat ttgctgtata atccagtgta cattaattat gaatttacaa at

#ttatattt 114300

ggagtacatt tgtagcttaa aaattttgga tgtataatat ttgttagata tt

#tttatagg 114360

cagttttgct ttgttaaatc attcttcctt tcctttaaaa taaaataatg at

#tctattta 114420

atatttttga tggagtactg taggatattt ttatatttaa tccttgtgaa ag

#aacatatg 114480

cttcctatac taggttatat attttgtggt atccttattc tttggaaaga tt

#aattagtt 114540

acaaaactta caaatagctg tactatcatc ttgatttcag aaagcaacat at

#ttaatgta 114600

gtcactaagt attactatgg attttttcat tttaaatttt tgagaaaaat at

#tctcaaat 114660

cattaaacct gcaaaagaac tatctaggct aaaaaaaatc ttctcagccc ca

#ctcatatt 114720

tgccagagct cattcctctc tcggctattc tcactttgat ctttggccct ca

#tttcatta 114780

acatcagagc ataagatcaa ttactagagc agataaattc ttactcccct aa

#aaacagag 114840

tttcataaaa agctactcaa gtgaattaga aacaagacat agatcttgta ca

#atttacat 114900

taaagtcact gcttgtcttt cactgaggcc ctatgcataa aaattgatat tt

#attgttaa 114960

ggatattttg cattcatttt ttagacttca ccctttattc ttagcatttc tt

#ctcgttaa 115020

tgatcacttt tgctttgtgt acattcattt cgatcacaaa catctcatgt ca

#gaaattca 115080

actatagctc ttcagtaact ccaaatgtta atattttttt cttatttttt tc

#tactgtgt 115140

catatctaaa ttctcagatg aaaaaccaat attgaagaat taccaggcca ag

#tatataat 115200

gtgaagaata tagaacaact agaaaagaga agaaggttaa agtcataatt ta

#tactgtaa 115260

agagaaacag gattatattt cttttgacat aagcatattt gagtatcaat ta

#aaatgtat 115320

tatgtacaaa aattaggtaa tgtagtataa aatattaaat ctgttggcaa at

#gctaatta 115380

aattatggtt aaagaatagt tatttaactg aactcacata cttttccctg tc

#taaaattt 115440

caagattgtt gaggctggag aaacttcttt taaaaataat aaatagaagt ac

#cagagtac 115500

tcagcttatt gatgacaagt taaaataatc cacaagtaaa gaaaaaaggt ta

#ttatagaa 115560

aaagggcaaa tgagatgttt aactgtgtgt atttatttaa actatattta tt

#catggatt 115620

actatatgtg aagcactgtg caagaatatg atttaccaga tttttccaat tt

#tgatttat 115680

catatttacc tggtgatgct tgcaggttga tctgcatttt atgaaaaaga tt

#cctccagg 115740

tgctgaagca tcgaacatct tagtgggaga actggagttc ttggatcgaa ca

#gtagttgc 115800

gtttgtcagg ttgtctccag ctgtattgct tcaaggactg gctgaagtcc ca

#atcccaac 115860

caggtaaaaa gtataaaagc gtcttttgta tttttcttaa accatctttt ca

#tggaaaga 115920

aaatgaggat tcaatgtaat tttctgttag agttttgact agaaactaat gt

#gaaatcca 115980

caaaactact attaattttt gtttgtggag gaggggaaaa gtgctttaaa aa

#ttattctc 116040

ttctttcctc ccttctctca aacttctgct tcattttagg cacattcctc at

#ctcaaggt 116100

accctgaagc catatgaatc cttttttttt tttttttttt tacatttttg gt

#aaaagaag 116160

tggtaacatg ttagcttttt ctcaaagatt gcattaaatt gtctgctata ga

#aagaaagg 116220

atcctgtgca tgagtgcggt caaactcaaa aacagcaaag ttactaaggt tt

#gcttacac 116280

ttgaataaga aggccttcaa aatgcatgta agtgccatcg ttaggatagc gt

#caaatata 116340

tgtttcaatc ctaggcacag tgggcttccg acacacaggg tctgtagaaa ca

#ctggtaga 116400

agtattatcg cagtgtggtt ggatgtgagt taaaggtaca aatttaattt ga

#tgatcaga 116460

acttgtttct catttaacaa taaaataaca acttagggat aatacaaact ga

#attatgct 116520

tttctcattt tttagaataa ggctatccat tactaaaact gtaaaaaaaa ga

#aaaagata 116580

aaaaaaagaa aggaaacaca gaatattgac tttagcacat taatttccaa gc

#aatttacc 116640

caggaacctt gttttcttcc atacttctac catcagtgtg attccaaaat gc

#agatagcc 116700

ttttactcta gtcctattcc cacagcaaaa catgtatatt tagggccccg tt

#cccatatg 116760

gctggtgccc tttgtttgat gctacagcta tctcaaaagc tgttagtgcg cc

#tcctcttc 116820

caaacattga ataccttagc caagttactt gatgaaaagt tcaggtactg ta

#tcaactgt 116880

agaatatatg tcctctatga atctttggcc ttaactcaaa atatagcaga tt

#acataact 116940

ccatgctttg attatggata aaatattcta caactatgga acagcacagc ca

#ggagaggc 117000

ctcatttttt aagagctcag ctgactggaa cgggattcag tggttaagta cc

#tatgtctg 117060

actatggttt gggggaggaa tctagttact gttcagatta tagaaagaag tc

#tatgttta 117120

tcctgtttga gagttactga gatgactgat acacatcaac ttttatgtac aa

#agggaaag 117180

gatgaactga gcacattaaa gtggcatctg actgtgtgat tcaggctata tg

#ttttctat 117240

ggacaacctg taacctattc aaggtttctg ggagtctggg atttatatct aa

#gatgttaa 117300

acttgctaat ggtagagtta ctattatagc agtttaaaat ttcttttcag tc

#ctccaagc 117360

agtgcatttg tgttccacca cttaggaagg tgtctggtga actatgagca aa

#tgatggct 117420

atttacgaca atgatagtgc ttgtatttca aaagaaggaa aagaaaaatt cc

#catgagta 117480

gaaaaaagcc gtgatggggt tatataccct tactgtgaaa actgtcaggt tt

#aagtgacc 117540

ttatttcata ctgagatagc aaaatatgtg tagagaacaa cggagaaaaa aa

#ttagggcc 117600

actgtagagc aactgtatga gaaaagattt aaagacaaga ctatttagtt ag

#gaaaggtg 117660

aaaaatggaa gattagttgg acaaacaaaa taaagaaagc cattcagggt tt

#cttattat 117720

cctttttttg ggaagacaaa aggcatccta ttaatacgat ggcaacacat ag

#tagaaagg 117780

tcagaaaata atcttttaga tctttaaaaa tagcccatgg aatggaaacc tg

#aaaaatag 117840

caagatgtac ataggttagg aagtttctta aaaagctatt atagttgata aa

#gcacctgc 117900

taccgaatta aaccattcct gtttttaatg tatactggac atttctacat ag

#tagaaatt 117960

ggcttgggtt cagttgtcac tggcacacac aaaaaatatt gtcatatcct ct

#acaattgt 118020

gtaatatttg cctcatgtaa aaacatgtac aatctctaaa gattacaact aa

#atgaggag 118080

tagaattata gtaactattt tagtacacct tgtgaagtca ttagtcttca ta

#cttaacag 118140

cataaaccat ttaacaaatt aacaccacag aatgatatgg cagaatatag gg

#cattcttt 118200

aattttcaaa atttcccaga aggattgacc ttctcagaga cagggcaatt ac

#cagtctgc 118260

taaagttaga gtatctattg atttctttaa aagcaccact tgtgatgatg aa

#tttgccaa 118320

atgttcgacc taatatagat ggaatattat agtgcagatg ctatttttat tc

#ctcagcat 118380

tataaataat agatcattaa ctccccattt tcttctacgt ggctgatctt tg

#attcctga 118440

caataatttt ttataatgaa aattgcacat acacctactg ttttttgact ct

#atattttc 118500

tctgttttgc tactgtgtta cctttgtccc ctttgaacta ttcgccattt tg

#catacaag 118560

tgagttttct tccttccaat ttagaaaggt ctaatcagat tttacttttc cc

#actttcct 118620

tctctaagga tcatagaatc cttaaaattc ccaataacaa ctgcacatgc tg

#tacagata 118680

actaaacgga gaaacactgt gataaaaaaa aaaaacacgg aaaaccatgc at

#tcccattg 118740

cttgaggatc ttaagcataa gggtcaatca tggtaaaatt tttcaaaata at

#aatgaact 118800

atgaaaaact atggaagtat ttgccatcac aatctccatt ttcagtaatt cc

#tttgagat 118860

gagtgattct gtattactaa aattattttt atatttctac cttaaaacat tt

#tttttctt 118920

cttaattaca gatttttgtt cattcttctg ggacccctgg gaaagggtca ac

#agtaccat 118980

gagattggca gatcaattgc aaccctaatg acagatgagg tatttattca ag

#ttctttgg 119040

gaacattttc ccccattagg tatacctaaa acttttggag gtcctctttt ca

#tgacagtt 119100

tgttgtgaat cagatttctc tgtattgaat cccattctcc catgcttctg ct

#ataaaatc 119160

tcctttagaa aaatgtttcc caaagggata ataaattaac acccatgaat at

#aatatttt 119220

aaaacttcat agtgtaaaga aattttttca gtgacactta gaatatatta tt

#aatattcc 119280

ctttatggta tatgtgctac caaagtaagc accattgtta atatcaatgg aa

#atcttgtt 119340

ttgagtaaag aatttcgaag tctaaagaaa aaacaatagc agtttatctg aa

#tagtatac 119400

atgacaccaa aatgcatgca acatctatca actctctaca gttgcctgaa tg

#tagatatt 119460

tttaacctgg gagtctgggg actattagag aagctgtaga tagatttcaa gg

#agcttgtg 119520

atttctgtaa cagagcatgt aaatttttct atgtaaaaaa tttgtatgta ga

#ttttttgg 119580

gactggaaaa agctttcatc agctcttcaa agaagtgtat gtctcaaaaa ta

#taagatct 119640

ttaaagtaag aacataaaaa gtagcatcat accactattt tcctttactt gg

#gttctcca 119700

acacattatg gaaatttgtt gttattgtta acgggaagag cagatgcagt ag

#atcacaga 119760

aggggcatta aatcaaaatt cagttgtaaa tgaacaaatg ggattatata ct

#tctagatt 119820

tcatctaaat aatttaataa tgtttttatt gaaatacatg gctgcagata tt

#tgaaaatt 119880

ctgtaaaaag agccaattag tattgtatat tactttttct atgtttacaa ta

#gctaaaat 119940

ttgaacttgt tttgggggtt aaatattata aattcttcaa tctgtccaaa tt

#atgtttta 120000

tagtgttata tgaattagtt tttgatattt atgcacaaga aagcaaaagc aa

#gaagaaaa 120060

acattttttc cctcagtttt caaaaggaac caacttaatg agtgtattag tt

#tacaacga 120120

ctgccataag aaactactac aaattgggtg gtttaaaatg acagtagttt gt

#tttctaac 120180

atttttgagg ctagaagttt gaagtcaagg tgtcagcagg gccacaatcc ct

#tcgaagtc 120240

tctaggggag gatccttcct tgtctcttcc atattctggt ggctcttggt ct

#tccctggc 120300

ttgtggcaat agacctttgt tctctgtctc catcttcaca tggctttctc cc

#agttgtct 120360

ctgtgtgtct tcttattttc tgttatgaag acagacattt gtcatttgat tt

#agggccca 120420

tcctaaatcc atccaaatca ttggatttag ggcccatcct aattcaggat aa

#tttcatct 120480

tgagatactt accttaatta catctgcaaa aatccttatt tcaaataagg cc

#acattctg 120540

cggctccagg ttgatgtgta ttttgggagg aaattattca atccactgta at

#gaataact 120600

tattctattt aggaaatttg tgagaagaca ggaggatgaa aaaaataact ta

#atgagggc 120660

catacacctg atttagcaga actctctctg agaaaacact cacagtataa aa

#gctcttag 120720

tatttctata ttgatttgta ttgttattct atgatttaag tattatcact tt

#cacataca 120780

tttgtttaat attttgttat atttcagaca aaaaatgttt ccccatctaa ga

#aattaggg 120840

caatatttta agatatctgt ggggcatgag acacgtgata atgtgagagg at

#cctactat 120900

gtcatgggaa gtacatgtat atcaatgtat ctctcttctc ttcatcctct ac

#ttccccaa 120960

ttgggaatca agatttttct cgacagaaag atgtcagttc caaagttttc tt

#gactaacc 121020

aagtggacac agaacaggga aacatccatg ttctataaat ttcagattta gg

#atgagaac 121080

agagaagggg cttccaccta tttctttgat tagtgagagc tacctaattt ga

#gaataagc 121140

atcaatcaca taataaagac tgaaatttga gcataagcat cagtcatcta tt

#ttttcaat 121200

tatttagact tgaaagtttc agagcatggc tttaggtaat cattgtagat ta

#tgggatag 121260

agaagcagaa actcaaccag aaagctactc taaaagataa gagccattag tt

#ataatagg 121320

acatgttaat tacaacagga cattgattga atatcaaaga atgtttaaat at

#tttttaaa 121380

agagaaaaca gatttgtatt tctcaaagcc tcggtgaggc aattgttctg ct

#tatctaat 121440

tgctttgaag gctattgaat aattgtacta ggccaggtgt aatggcttac at

#ctgtaatc 121500

ccagcacttt gggaggccaa ggtggatgga tcacctgaag tcaggagttc ga

#gatcagcc 121560

tggccaacat ggtgaaacct cgtctctact aaaaatacaa aaattagctg gg

#tgtggtgg 121620

caggtgcctg tggtcccagc tacttgagag gctgagaggg gagaatcact tg

#aacctggg 121680

aagtggagat ggcaatgagc caagattgca tcactgcact ccagcctggg tg

#atggagcg 121740

agactctgtc tcaaaaataa ataaatagat aaataaataa gaaagaaaaa ga

#aaaaagaa 121800

aagaacaatt gtactcatta agaatagaat ttaatatgtt gattcatagt tt

#actttggt 121860

taaaaaaaat agtgcattgg agtgcattat caaacataaa ttccatgaga ac

#agttagca 121920

ttttagcatt cagtattcgt ttttatgacc tgattcttcc aagtgctcaa at

#aaatatcc 121980

attgagctaa gttctgtttt ctttcccttc tctgtacttg gaacactttc ta

#ggtagact 122040

gtcttccttt tgtattttta gacttattat gagtgtctga ccctcagtca gg

#gttcaata 122100

aatctttaga acatgaatca attactgaat attctagaca tcataccaat at

#tctatctt 122160

gaatcaagcc aataatttat tttcttcatt tctgttgagc tttgctagag at

#aaatcata 122220

tgattatgct tatcaacact gctaccaatg tgttgatccc ttcacattct ca

#aaaattac 122280

taagcacccc aaagaacttt tgtgtatgta gatatgttgg tatttaccat ag

#gagaactt 122340

aaaactgaga aatttaaaaa gtatgtgtta atgaattcat ttaaaaataa ta

#atagaacg 122400

ggttcagtgg ctcacacctg taatcccaga actttcagag cctaaggcga gt

#ggatcact 122460

tgatgtcaca agtttgagac cagcctgggc agcatggtga agccctgtct ct

#accaaaaa 122520

attcaaaaaa atttagctgc atataatccc agctgctcag ctacttggga gg

#gtgaggtg 122580

ggcggatcac ttgagccagg gaggtggagg ttgcagtgag ctgagatggc ac

#cactgcac 122640

tccagcctgg gcaatagagc cagaccttgt ctcaaaataa atacataaat aa

#caatagta 122700

aagccattac atattaacat aaataataca ttttaatgaa aacaaannnn nn

#nnnnnnnn 122760

nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnagtt tgtattgagt at

#caaaccag 122820

aaatggaaac aaatggtcta aaagtaaaat agaatatttg aaagcagaat tt

#tcctggca 122880

attttgggac atttggtcac tgtaatttag gccagcataa agaataatat ag

#gagtcctt 122940

aatctcaaat acttgtatca tttcatccca agtaaaattt aaagtgtcag aa

#atatttat 123000

attatattca gtgtaaatta attttttctc ttcatcctta tttttatttt cc

#ccacttac 123060

tatattaagt acgtaattcc tgagtatgat aagataaatt aggttatgct gc

#aggaataa 123120

ccaactaaaa tattaatggc ttaaaacaat aaggatttat ttctatcatg ct

#aaactttc 123180

atcaagatgt aggagagagg ctctgctcat tataatcact taggccccct gt

#gcttatag 123240

aagctctagc tggacctgtg ttttctcagt cactaaacca gaaaaaaagc aa

#tgtgataa 123300

gtcacacatt ggtactcata acttccattc aaaactgaca tatgtacacc ca

#agtagaat 123360

atacctgatc caaatagcaa agaaggcaaa gaagtacaat cttaccatgt gg

#tctagaag 123420

aaaacctgga atatctgtga acagcctaaa tggctaacat agcacatgtg tg

#cggagggg 123480

aggtggaagg gacaagtatg aaatgtaact catactttga gtggaaatga ac

#tttctgca 123540

ctgtgtagat ataatatata gttggccctc tgtatcttca ggttctgcac cc

#ttgaactt 123600

aactaactgc aaatcaaaaa tatttgaaaa gtcagggtgc agtagctcac ac

#ctataatc 123660

ccagcacttt gggaggccaa ggtggaggat ggtttggggc caggagttca ag

#accagccc 123720

aggcaacata gcaagactct gtctctacaa gaaatttttt aaaaattagc ca

#ggttttgt 123780

ggtacacacc tgtagtccca gctacttgga agacaggagc ttaagcagga gc

#ttaagcct 123840

aggagttcaa ggctgcagtg aggtatgact gtgccactgc attccagcct gc

#atgacaga 123900

gtgagaccct gcctctaaaa acaaaaatca aaaatattcg agggggggac aa

#taaaaaat 123960

aacaatgtta caataaaaat aatatgcata aaaattatac agtataataa at

#atatagca 124020

tatacattgt atagatatta taataatcta gaaatgattt aaagtacaga tg

#ctcctcaa 124080

ctttcaatgg gggattatgt ccccccattg aaaatatcat aagtggaaac ta

#tgtttttg 124140

acttatgata ttttcaactt atgataggtt tatccagact taaccccact ga

#aagttgag 124200

gagcctactc aatgcatgtc acttttgcac catcataaag tcaaaagatt gt

#aagagaaa 124260

ccatagaaag taggggatcc tctaaatata ggagtatatg cataggttat gt

#gcaaatac 124320

cactccattt tatgtaagga actcaagtat ccatagattt tggtatctgc ag

#ggaatcct 124380

ggaaccaatc cctcaaagat actgaggaat gactatatat ccagaaaata ct

#aacataac 124440

cttagtatta ttttcaaaat ggaaacaaaa ttaacctttt aaattaattt at

#ttatgcca 124500

gggtataaat actgctgaaa tttccaacac attttacaaa tttttatttc ta

#tttgtaag 124560

caaaggcttc ctccagaaac tgattttccc atacataaat aacttttgcc ta

#attctagt 124620

ttaatgagct tcctttcatc ctcctttttc tttcccttac tccttccctc ta

#gaaatttc 124680

aacattcatc tgacatcata agacaaatag ttacctatat ggatccataa aa

#taaattat 124740

aatattttac aacataaact tctttagagt cagagctgtc tatttcttca aa

#ttgttata 124800

atcacatgtg agataactga gttgaaaaca ctgaacacat taatatttta ta

#attatttt 124860

taagctataa ataatatttc tatttcttct aaaggtattt catgatgttg cc

#tataaagc 124920

taaagatcgt aatgacttgg tatcaggaat tgatgagttt ctggatcagg tt

#actgttct 124980

ccctcctgga gaatgggatc caagcattcg aatagagcct cccaaaaatg tt

#ccttccca 125040

ggtatgtata tttgaagaca ttctttgaaa ttgaattttt ttttgtcttt ta

#aatgcatg 125100

ttttatttta ttttatttat ttatttattt attttattat tattatactt ta

#agttttag 125160

ggtacatgtg cacaatgtgc cggctagtta catatgtata catgtgccat gc

#tggtgtgc 125220

tgcacccatt aactcgtcat ttagcattag gtatatctcc taatgctatc cc

#tcccccct 125280

ccccccactc cacaacagtc cccagagtgt gatgttcccc ttcctgtgtc ca

#tgtgttct 125340

cattgttcaa ttcctatcta tgagtgagaa catgtggtgt ttggtttttt gc

#ccttgcga 125400

tagtttactg agaatgatga tttccaattt catccatgtc cctacaaagg at

#gtgaactc 125460

atcattttta tggctgcata gtattccatg gtgtatatgt gccccatttt ct

#taatccag 125520

tctatcattg ttggacattt gggttggttc caagtctttg ctattgtgaa ta

#gtgccgca 125580

ataaacatac atgtgcatgt gtctttatgg cagcatgatt tatagtcctt tg

#ggtatata 125640

cccagtaatg ggatggctgg gtcaaatggt atttctagtt ctagatccct ga

#ggaatcgc 125700

cacactgact tccacaaggg ttgaactagt ttacagtccc accaacactg ta

#aaagtgtt 125760

cctatttctg cacatcctct ccagcacctg ttgtttcctg actttttaat ga

#tcaccatt 125820

ctaactggtg tgagatggta tctcactgtg tttttgattt gcatttctct ga

#tgaccagt 125880

gatgatgagc attttttcat gtgtcttttg gctgcataaa tgtcttcttt ta

#agaagtgt 125940

ctgttcatat cctttgccca ctttttgatg gggttgtttg tttttttctt gt

#aaatttgt 126000

ttgagttcat tgtaggttct ggatattagc cctttgtcag atgagtaggt tg

#tgaaaatt 126060

ttcttccatt ttgtaggttg cctgttcact ctgatggtag tttcttttgc tg

#tgcagaag 126120

ctctttagtt taattagatc ccatttgtca attttggctt ttgttgccat tg

#cttttggt 126180

gttttagaca tgaagtcctt gcccatgcct atgtcctgaa tggtaatgcc ta

#ggttttct 126240

tctagggttt ttatggtttt aggtctaaca tttaagtctt taatccatct tg

#aattaatt 126300

tttgcctgag gtgtaaggaa gggatccact ttcagctttc tacatatggc ta

#gccagttt 126360

tcccagcacc atttattaaa tagggaatcc tttccccatt gcttgttttt gt

#caggtttg 126420

tcaaagatca gatagttgta gatatgcagc gttatttctg agggctctgt tc

#tgttccat 126480

tgatctatat ctctgttttg gtaccagtac catgctgttt tggttactgt ag

#ccttgtag 126540

tatagtttga agtcaggtag tgtgatgcct ccagctttgt tcttttggct ta

#ggattgac 126600

ttggtgatgc aggctctttt ttagttccat atgaacttta aagtagtttt tt

#tccaattc 126660

tgtgaagaaa gtcactggta gcttgatggg gctggcattg aatctataaa tt

#accttggg 126720

cagtatggcc attttcacga tattgattct tcctatccat gagagaataa aa

#tacctagg 126780

aatccaactt acaagggacg tgaaggacct cttcaaggag aactacaaac ca

#ctgctcaa 126840

tgaaataaaa gaggatacaa acaaatggaa gaacattcca tgctcataaa tg

#catgtttt 126900

acaatagcat aacccatcaa gaagattcaa atgatttaaa ggatagcctc ta

#aggcagaa 126960

ggggcatgaa gttacaagat ctttcttagt actacctaac acacattact ga

#gaaacttg 127020

gcagtttgat gacaacctac taatcaaaca gtgccatatg cctggaaaga tt

#ttagcccc 127080

tacttaaaac atattatcca agaggaatat taaaatttta ataacaacat ta

#aatatggc 127140

ctaagagaaa gcgcattact gtccttgtat gttttgatac atcactttga aa

#ttggcaag 127200

cattaggaaa attcaaagac atgacttaat catattatat agaaaactcc at

#atttatta 127260

ctgctaatca caggaaatat tgggaagatt ttaaaattat aattcttata tt

#tgtattgc 127320

ttttttgtga atgtatgata taaagatttt ttaaattttg tttatgaaca tc

#taatgtat 127380

attttaccca tcatacaatc cagaaagata gaaatataaa gcattgctat tt

#tttagggt 127440

cattttttaa attgcaggca tgagtattaa gagtgatgac caaatatttg tt

#aagctcac 127500

tcctcatact gccacctcta tgcctactga atctgcctcc cacaaccctc cc

#aaattgtt 127560

gtgtacttag tcttgccttt gcgccttgcc ctgtggagtt cagccttgcc tg

#actctgct 127620

accctattgg aagcggcaga tggtctaatt gacccagccc tggaattaga aa

#ttttcctg 127680

ctttgccaga ggtgggcaaa tgagcagttg taccactcaa ccatgagtac tt

#aaaaaggg 127740

tatctcaatt tcactgtcaa tttaaagaaa ctatatggat acctcatttt ta

#tattttca 127800

ttttgaaatc atttcataat tattaaagac tatttccttt tctcaaaact ta

#ccattttg 127860

tgattatgta actgctacca catatttcag ttgatctact attaaaataa aa

#agttgcct 127920

aataattaat tgtagggttt atagattgtc tcatttctgt acttgtagaa ta

#catctttg 127980

tactaatgat attagaaaag gcaatataat gcttcctgag tatgtagaaa ct

#ctttaatt 128040

aatgttattt ggagaaatgc agcaaaatat taatacattc agaatgaggc tt

#taaaattc 128100

actgtaatac ccattagcta ttgaaacatt gaagttaagt gtttttgaaa ac

#acctttgt 128160

gaacaataat gtttttgagg caagttgagt gatgggaggc caatattgtt ta

#tgatttta 128220

tgacaccctt taaaatcgaa ttaattattg gattctgggt attgagaggc ag

#tcatagaa 128280

agaacatcaa attaagaatc aaagcatccg agttctgcaa ttatctatat gt

#atgacctt 128340

gaacaaatgt tttaacctct ctgttgatgt tctgtatcag cactgtccaa ca

#gagttttc 128400

tgcaataatg gaaatattct acgtctatgc tatccagtaa tcaagccact ag

#taagcatt 128460

agaaatgttg ccattgtaac taaagatcag aatttttcat tttaattacc tt

#aaatgtaa 128520

atagacatat gtagtttgtg gctatcatat tagacagcat agttctatac aa

#caaatttg 128580

aaattacaga tatgctctat gcttcttttc aacattcatg ttttaaaaat at

#atgttgta 128640

attgaataat agatagcatg aggctatgtt ttctattaga cggagtgaaa tg

#agttaata 128700

tacattaaac attctgacct catactcttt caaatttttt caccattggg at

#catttcca 128760

tcttttttat tcatttgaaa tgtgcaaatc ccagcatttt aaatattttt tc

#cctttcag 128820

ttaagagaag aataacctgt cacctccagg gataaccctg aaaatgttca tt

#agaacttt 128880

gcatcagtca ttaaaatcac tcccttttgt gtaccctcaa cttatttgct ct

#tctctcat 128940

gtcgtgtact tgcttggcaa aaccacaacc ctgtgagaat ccaacacttt ac

#tctgtacc 129000

gcactgatga actgaagctg aaggaaaaca tgtaaccaca ctaactggtc tc

#acataaat 129060

tcatgaccac atacctcaag tgagcccttt gtgttgcagg ttcatcatac ta

#cactttcc 129120

tagtccaatc attctcactt gatgactatt tcacacttat tcttctctcc tc

#aagccttc 129180

agcacatcct ttctgaccct cactctcata tgctgatgtg ccttttattt cc

#ctaagaaa 129240

tttgaaacaa tcaaaaaaga acttctatag attgctacat gcatccacat ac

#tctgcctt 129300

cctgttcatt actattgatg aaatagccaa agtcagcctt ctacttgtgc ac

#tagaaaga 129360

acctatctct tcacatctac tcaagagcac aactctacca attctcctct tt

#ctcttcta 129420

tatcatcaaa tctttttttc tgtattttat cacttttatt agcatacaat ac

#tattaaat 129480

ttaccaatct taaataaaag aactctcttg ataccactac ccagcctgcc ac

#tcttattc 129540

attccctttt ataacaaaat gccacagaag agttctctgt gctacttgtc tc

#cagttact 129600

ctcctccaat tctcttttaa cattcactcc aagaggcttt tgcccctacc at

#ttcactaa 129660

aatacatacg agaacaatga tctccaccat gctaagtccc atggtcaatt ct

#cagcctgc 129720

attttatcta atctatcaat gaacagcatt taagagttga tgactccctt tt

#ccttaata 129780

tatgttcttt acttggctcc caaaacatca ccttctgtta gttttgtcat ta

#taaaatag 129840

agttaattta tctagtcagt agtattttcc cagaagacca cataataatg ct

#tgctttct 129900

gagacctgtg aaagctatga attgttttcc taggtgattg ggaagtaggt at

#tgagggaa 129960

actcttaaat ccctttatta atgtatccta tttacctgta aagacagttc ct

#tcatcagt 130020

tgacagatgc ttctctttta tctttgaact ttagtcttac tgcgtccatc ca

#tttgcctg 130080

ggaaaattgt taaaatatta agcaataaac tttcttatat tgagcatttt tc

#aaaacctt 130140

ttttatgttt taaacctgta tcattctatc taaatgtctc atggtaagtg ag

#atcagttt 130200

ataagtcact tttgtttttc atgtttacac taattctatt ttggaatggt gg

#tcaagtaa 130260

aaatcataat ttcaccactt aagatttttc ctattatcct ttgaagtgct tt

#tgaacaca 130320

ttggtgtgct ctaagatcac cataggtagg attttaggta gaactttctg at

#tttttaag 130380

aaatcatatt caccaacaaa agcaggtgga atagaccatg ggaaaacaat ac

#ttacctga 130440

atctctacta atttgtcatt ggttaaatta gaagcctcct tttacaacag tc

#tttggcac 130500

tctatgagtt agaaagacct atattgtaaa ctatttactg ggtagaaaaa ca

#ccagctgg 130560

aattacacag agaaatatac tttaaaaata gtgatgatgg ttactgttct tt

#gaacagtt 130620

aaactatgcc acgcatataa caccaccata cttaacacct cctcacgcca ac

#ctacccac 130680

atcctgatct ctctctttgc cccttccctt acttcatttt tcttcatagc tc

#ccatctgt 130740

acctgatatt ataaggttat tgtctcttca ctaacagaat gctttttctt gc

#ccaccttt 130800

gcagctctag cattcattac aatgaatggc atacactagg cactcagttt ta

#gttgaaag 130860

aataaataag tgcccatcac ctcatttaat tctcttagtc acactataag at

#agatactg 130920

ttgttacccc cagtaaacaa aggaagaaac taacacttta aaaggctaaa ta

#acttcctg 130980

gaggtcaagc aacaagtaag tacagagcct gggttctcag ctattgtgca ta

#ttgcttca 131040

aggaaaaatg aactgttatt attatttaca attaacacct gaaattaaaa ca

#aaacaaaa 131100

cacatgaaca aaaaactctc cacaggagaa gaggaagatt cctgctgtac ca

#aatggaac 131160

agcagctcat ggggaagcag agccccacgg aggacatagt ggacctgaac tc

#cagcgaac 131220

tggaaggtta gtgaaaatca cttctatggg acttcaagga ccaaatgaca ta

#ccattctt 131280

ctctgtcaga aattgctatt ttgggatcta atttattgta tacttttaat ac

#ctgctttt 131340

tgagggtgaa aatgccaatt agtttgattt ctctgaagtt actaatgatt gt

#cattactg 131400

ttaaactaaa acagtggata cacccttcca ttatacttta cctagtcttt ca

#ttttgctg 131460

tgcataaaat gcattctcag attcttagaa tgaaaaggaa aaccgtcaat tg

#acccttcc 131520

aaaagaaccc attgaaagct tcaagttgaa gatagaaata aaactaaata cc

#aacaactc 131580

agtcttgtag gccctatctc attaaatgca agtaggatgt atatagtggt at

#tttttatt 131640

tttatggctg tgatttgaaa gagctatatg atttattttt ctaatcacac at

#ctttgaag 131700

agatgaaagc ttcaatttat ttcttaaaat ggtgcttcat ggtttttttg ac

#agcttgtc 131760

tctctctaag caatgtgtga gcagaaaatc agaaaccctt gggtgggtct ct

#cttcaggg 131820

aatatgtgta tagcctccat tataattaaa ggcagttgca aaggctttgc ag

#gattggtg 131880

ctcccctccc ctcaaggcca ttttctgtac tgcttgcaat gtgtcctcta ag

#ctgacttt 131940

ccagttcctg agcactctgc attttaattc tgtgttcttt ccctttatct at

#gtgttgtc 132000

tctgaggaaa tgtcctttaa tgtcttcctc aggcttgata cctaatttga ga

#tggttcaa 132060

acaatttttt ccttttccct tcactggaag ctttgttact cattctgttt gc

#tttcatac 132120

tttcaaatgc tgtcttttta tttttggtgg tatttttttt ctctttctca gg

#tgtaacat 132180

gccacatagc ttagattttt ttcgaagttc acttttcctt actgcttcct aa

#atcctccc 132240

aggtcaccaa tatccggtat cttcgcttct ccagagttct tccacagatt ct

#gttgctga 132300

catgacttga agtatccatt actcatctgc tctcctggag ttgctggtgt ac

#atctgggc 132360

tgctcttgca ctgttctctg taatgaactc ccacttccgg atttagattt tt

#actgctaa 132420

aagcacattt attacacagt actataacaa ctattcagac taatgtatgc tc

#taataagt 132480

aattgattag aatcaatggt ctaatataaa gtgctttcaa aactataaat at

#taattact 132540

aattaatagc tcataaccac ctcaaattct ttttgggatt aggtgggata ta

#aatcataa 132600

atgaatgcct aaatagactg gtagagtaaa tctgttttga attgtgactt tg

#ataagtta 132660

acaaattatt cagaaatgat ccctaaaata aaaaaaagtg catatgtttt ac

#caaacatg 132720

ggtagagaag cctaaggtga tctttatgtg tacaaatatt tcacaggttc tc

#tgcaagct 132780

tctctgagtt tcaaatgtcc ttttattcaa ttgaagtttc attcttctca ac

#cctctcct 132840

actccatagc tctctaatgg aagcaatcac aggaaaatat agtgatctta ta

#cctgcata 132900

atagtagaag agttattaat aggtaactat tacagataaa tcagatcagg ga

#aattactt 132960

ggtaaaatat tttaattatt cataatatgt acatctttta tttcaaattc ta

#aggagaat 133020

ttatttctaa aaaggacagt cctttctgag atgattctag gactgccaaa tg

#aatattcc 133080

tatgcataaa ataaataaga aaaatgaaac agttttttat gatccaagta ta

#ctcagcat 133140

gctggcagta tattggagca taataagatt tttcaccact gacattaacc tt

#catgtagg 133200

aacttattca tagtcttatt catttttgct atcacatcat tattccatgg ag

#caaaactt 133260

acagtagcca aatgttaagt ctgcgtattg ttattaaatg ttcataaaat ga

#gaatacct 133320

acttattaat gctctcattt cttatagatt taaaaaaaga tctcaaattt ca

#agcataat 133380

ttcacagttt aatacttttc ccccaaaata attatctttc aagtgtttca ac

#atggtttt 133440

gaatatattt ggagtaaatg aatttatacc aagtaaggtc actattgtct tg

#tgaatcac 133500

agatgctggg atatgttaac gcaatagtgg atcaaaatta catttatcta gt

#tttattat 133560

tataaggact ccctcctagt tttctaaaaa tgaaaacagc tctgaaacct at

#ctgtctct 133620

actaagtatt gctgccatcc aaaaggacat ttagatgtct tcctgcaaca at

#atctggtg 133680

agggattttt gtttgtttgt tttttggccg agagagtagg taactggagc ca

#tggttaaa 133740

cattgctttt tctctctagg gtgatgctca ctactggagt atacaaaagc ca

#gctaaccc 133800

tccctccctc acttcctgct atgctaaatg gaattaaaca tttagaaata ct

#gccaatga 133860

ttgagggttg taggcctgag tttaggagga gtaggttgac gtagaaatgg ca

#cagagatt 133920

agagtaatcc ttgaatctca ttatttggat tatgattggt aaacagctct ga

#accttgtt 133980

taagagaacc tgggattttt ggtggttgac acgatattgg gttaggaatt ga

#ggtaacga 134040

acgtagttgt gcagtgcctc cctgtagatt gttataagac aatgcagcag gt

#taatgtgt 134100

gtctcacctc tgctgatgga aaacgtatac tgtgacctgg caacaaagca aa

#tgagcatt 134160

ttgacttgtg tgttttttat atttgggttt cactattgtg ttttcccccc tg

#tcttagga 134220

tttttggggg acttatttta gatatcaaaa gaaaagctcc atacttctgg ag

#tgacttca 134280

gagatgcttt cagcctgcag tgcttagcat cttttctatt tctctactgc gc

#gtgtatgt 134340

ctcctgtcat cacgtttgga ggactgctgg gagaagcaac tgaagggcgt at

#agtatgta 134400

ttatgctttt ctctgaactt tgaaacataa tccattttta agattcatag tt

#agataagt 134460

gagcatttaa ttttggattc ttttctgagg agagatttga gatatggtct gg

#cagataca 134520

ccttatatga atttcctgga tggctagtgg aactggtaat ctgggagtgg aa

#tgtctcag 134580

aataactagt tctgagtctt acaaaaggtt ctcatctgat gccttgccct ca

#gcgccccc 134640

aatcctaagc taggtttagt ctccattctt gtctcacaag aggtccattt gc

#tatgtacc 134700

cgggccatgt ttctgtccag acactaatcc tgaatacatt taaacctttt gt

#aaggcaac 134760

agagacgtga gataggaaag tgaagagaac actcctacct ttgctactat gc

#attttctt 134820

cttgctgtca gcccctttag tcatccttct accccacgtc ttgcccaggg tt

#gctagact 134880

tttcagggtg aagcacaaag cacatatcca tgtattttaa atgtcttctc ct

#tagctaca 134940

atggcctcct gtacagctta ggtaattgaa ccatttatat ctctacacag ag

#tgcaattg 135000

aatctctctt tggagcatcc atgaccggga tagcctattc tctctttggt gg

#acagcctc 135060

ttaccatatt aggcagtaca ggaccagttt tggtgtttga aaagattttg tt

#taaatttt 135120

gcaagtaagt gttatgtact ttttggccct tagcctcttc cttttttctt ta

#ctgtattt 135180

atacttctcc caacatcact tttggaggtc tgttgataga gacagaattg cc

#tgatttgt 135240

ttcagtttat catttttgct tcatcatggg aatagaggaa aagtaaaata tt

#tatgtata 135300

tttttatgta atatttttaa aaagtaagac tcagttataa gcatcgataa at

#cccttttg 135360

attttgtccc tttagatgtt ccctttagac cggtggtctg caaccatttt gg

#caccaggg 135420

actggtttca tggaagacaa tttttccaca aagagggttg aggggatggt tt

#tggaatga 135480

aactgttcac ctcagatcat caggcattag attctcataa ggagcacaca at

#ctagattc 135540

ctcacatgca cagttcacaa tagggcttgt gctcctatga gaatctaacg tc

#cccactga 135600

tctgacaaga gtctgagctc aggcggtaat gctcactcgc ctgccactca cc

#tcctgctg 135660

tgcaaccctt ttcataacag gccatggacc aggggttggg gacccctgct tt

#agacagtc 135720

ttgagtttag atactcatgg gatgtgaagc ttatttactt tcacttcctg aa

#tgaggttt 135780

attttcattt gcttaaaatg atagcaagct gttaaatgac cttcttttca ct

#gttctttc 135840

cttttcctcc tcccagagaa tatgggctgt catacctatc tttaagagct ag

#cattggac 135900

tttggactgc aactctatgt atcatacttg tggccacaga tgctagttcc ct

#tgtctgct 135960

acatcactcg gtttactgaa gaagcttttg cttccctgat ttgcatcatt tt

#catttatg 136020

aggccctgga gaagttgttt gaactcagtg aagcatatcc aatcaacatg ca

#taatgatc 136080

tggaactgct gacacaatac tcgtaagtac catttcccct gctggccttg gg

#gcttttct 136140

tttgacaaat attgctattg ttacaagaaa tatgaggaaa ttactcagca ga

#gaatgtgc 136200

cttaagttga ttcatgacct aaatcctgac tctcagagtc gaacaggatt tt

#aaaagtta 136260

tttaatcggc cactcatctg ctacttgcat tctcattata ccatctctgc ca

#agagtatc 136320

tttttaaagt tctatttgtc cagtgttctc taaaataagt agataaggaa cc

#aattccat 136380

tttaatatac acgaatttta ccttagcgaa atatatgtta tttggcgtta tt

#tcagggtc 136440

tttttaattt acaataatcc aaagaaacat agtaatgaaa atataagatt tc

#aaatttag 136500

agcaataagg taaaataaac ttattgggtc taaatcttag tagatgtttg aa

#agtgtggt 136560

aaaaacataa atcactgaat gaaaatttaa ttttggtttt ggcacttgtg ac

#attttgat 136620

ggaaatactc agatattagt tgttgaagtt gatgttacag tccgggattg aa

#gatgtgat 136680

tggatctatt gctttttcta gttttggtgt atcaacagtc tgaaatgtct ct

#aaggcttt 136740

gtctgcagac tatatgtggc cattaaatga ccccattatt taattgtaga at

#tttttatt 136800

gtgcttatat gcagtttttt atactgcaaa tatctgaagc aatatgttct tt

#aggagaca 136860

gttataatct ctgcatcaac caccaatcat ttccctataa actgcttaga ta

#tggccttg 136920

aaccctttta atatttttta atctttattt actatcagaa gtttaaattg tt

#gaaatcag 136980

accaaaatag tgcaatgtta taattttgtt aagaatgacg aaatgttggg ag

#gccgaggc 137040

gggcggatca cgaggtcagg agatcgagac catcctggct aacacagtga aa

#ccccgtct 137100

ctactaaaaa acacaaaaaa attagccagg cgtggtggcg ggcgcctgta gt

#cccagcta 137160

cgcgggaggc tgaggcagga gaatggcgtg aacccgggag gcggagcttg ca

#gtgagctg 137220

agatcgcgcc actgcactcc agcctgggcg acagagcgag actccgtctc aa

#aaaaaaaa 137280

aaaaaaaaaa aaaaaagaat cacgaaatga tattatgttg aaaataatgt ga

#gttttagt 137340

actttcactt ttatattata tttagagata actttaaaca actgacccct at

#ttttgaac 137400

aagaaaaatc aaagtggaaa tataaaataa ttttcccatt aaaagcaaat ag

#tgagaata 137460

ttgtaaacag ggctaagaaa ggactgagca taggtgtcag ggacactcag aa

#aacaggca 137520

aatgggaaga acagtttgat caaaaccagg gataacattg atacacgcct tt

#tcatttat 137580

ccttacctga aagagaatct cactgaattt ggatatcctt gctgggatat gt

#aattatct 137640

ctggttggat tttcaaatct actacatgcc aggcactata ctaggtgcta gg

#aaaaccat 137700

ggtgaatcat attctgtcct cagtgagctt ccagtttagt agggaatgta ga

#taaacaga 137760

cagcataagg aaatgagtgc cgggttaaga ggttggtaca gaatgctata gc

#agcacatc 137820

aggagagcac ctaacccaga tttgaggttc agagaaggct tcctggagga aa

#taatgtag 137880

aataaaaatg cagtagaagt taggaaggtg ctaaggaata gggcagaaaa gt

#agttcagt 137940

caaagggcat tcacaggact agatgcaaga gatgcattca tgctttaaaa ta

#tttgtctg 138000

aagttatata gatagtggta aaacaagaaa tggaatccag gttttattac tg

#atataatt 138060

ttcagtacac tgatgaatac agataaactc tccaaaagaa actatgtaaa ac

#aaataaaa 138120

caggtaaaat cagaactatt ctgtttcaag tggtaggaag gcacccattg cc

#taccctct 138180

cagctgttct ttgaaccttc atggtagctt cttaggtact tcagactgag ga

#acatagtt 138240

taaagtccct tggtctagaa aggaaaaaga ttggaaaagc aaggtctgag cc

#ctgaacaa 138300

ttttcacagc tctaaagtag aatgagaaaa atgcaaccaa taggcaaaaa at

#aaataaat 138360

aaaaataaga aagaagcatc agaaaaagag gaaactatgg ataatgtcag gt

#cgcagaag 138420

gcaagaaaca agaaatgtat cacaaagtct ttagagagga cagtggcatg ga

#catcaaac 138480

agaataagga aaagtgtttg aaaagagata cctggtagct ttaaaaaatt ct

#cagcaaac 138540

tattgcaagg acaaaaaacc aaacaccgca tgttctcatt cataggtggg aa

#ctgaacaa 138600

tgagaacaca tggacacagg aaggggaaca tcacacactg gggactgttg tg

#gggtgggg 138660

ggagggggga gggatagcat taggagatat acctaatgct aaatgacgag tt

#gatgggtg 138720

cagcacacca acatggcaca tgtatacata tgtaacaaac ctgcacgttg tg

#cacatgta 138780

ccctaaaact taaagtataa taataataaa attaaaaaaa aaaaacaact gg

#tattgggt 138840

tgggaaagga ggcagaatgg gaagccagtt tgcaaaaact aacaaggaag tg

#ggtggtaa 138900

agaaatggag aaagctgcat aggccagttg gtgtcaaaga aagtgggaaa ca

#gaatgcct 138960

tttgaggagg gcaatgaaat cgtaagattg ataatttgtg acagagaagg ac

#tatgtgtg 139020

tttgaaaatg ggagaataga gactggggag aggaaggcag caatgatgaa aa

#gagtcgat 139080

aaacgtggga ttgcaacctc ccaggagtca caaaatagta aactcaagag aa

#taagtcaa 139140

acaaatgctc aaaaggtaat ttaacaacaa gaatagcttt aaataaacgt ga

#acccaaac 139200

tgacatgaaa atagcaggaa aatgacgaaa aaaaaaaatt cgccaaaaaa ga

#cagtgaca 139260

caaacagtgc acacaacaca caagagcgag aagagcagaa tggaggagga ca

#agacaagg 139320

ccggtgctca gtgagagacg caccgtatga cacctagcag aggaagcgaa ga

#gggtagaa 139380

gtgctgannn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nn

#nnnnnnnn 139440

nnnnnnnnnn nnnnnnnnnn nntctgaggc atggctgtga caccctcttt gg

#gctctgca 139500

gttcctggtg tctccaagct tctggtgcca ccacgttccc cagagcctgc ag

#tgtaagtg 139560

gcttgcagta tgcctggtcc agccacagcc ttgcacagag ctggttcctg tg

#ccagtgtc 139620

tggaactgcc tgccccacca cagcagccag catgcctgac tgtgcacagt gg

#ccagacca 139680

tatgcttgct cacttatgca cccctcacct ctgtgccttt ggcagcgctg gg

#atccaggc 139740

tggtagcacg agctgagcac aacctgccag gcctagtggg cagaatgagc ca

#gagggccc 139800

aagcaaaact caggcaaagg caccactggc cacaaaggct tctggctgga ag

#aatgacac 139860

cccggggacc tcatgacagt aataacttgg cttaaaaggc tgggataggg at

#ctatgaca 139920

ttaacccaat tagtggcctt gggtaagtcc ctaagaacaa cctctagaga ca

#atgtctta 139980

actcaagaaa aaaaaagtag gaagaatatg gaaaatacat agggaataag aa

#gtctggaa 140040

gtattgtatt aataccaaac ttatagtact taaaggacaa aataaagggt tg

#caaaagag 140100

ttcaccttgt tggtgaagga aaccttgtac tttttattct ctgcatattt tg

#aattgttc 140160

aacttgcact gtatgcctgc attattttgt aatttctttc taaagatgaa tt

#ttgtgttg 140220

ggaaattcaa gtcctgtgac aaaccatagt atgagctaat ctgggggagg tg

#gtgctctt 140280

caaattagtt tccatgtaac aaaatttatt ttcaaattca ggaaaagagc aa

#cctacaaa 140340

actcaggagt aaaatgggca aaatgttcaa ggaataataa gtaggtttac tg

#ttctgttc 140400

atacatgtgc ttactcattc actcacttag ctcattcctt caacatccat tg

#atcttcct 140460

tgtgtatgtc agtgctgatg gtataaaatg aatacaatat ggtccctact ct

#gaaagacc 140520

ttagtgatta tcagacagtg tctggagatg tcctttggac atgatatcca ct

#caaatagt 140580

atttgttgaa ttaataaatg aggagagagg ctagaggata cacagttaaa ta

#attgcaat 140640

gtgatataac aagcactata caaggtgtct gtataatggc ctaagagaag aa

#gtaacaga 140700

gtgccctgga gagctcagaa gcattcatag aaaaaggaaa cctgaactta tc

#tctccatt 140760

tctgttgtac ctgccacatg agtttattgt atgtggcata cctatgtttc tt

#tctctctc 140820

tctcttcatt gtacctgtga attcccacat gcagatcatc actagatctg ag

#agtagtta 140880

cgcagagtag aatggacctc tggggaccaa ttggcagaga gccttaaaag tt

#ctaataag 140940

ttttatctgg tacaaaggcc atcatggatc atgacaaggc tctgggaaga at

#tatgtgac 141000

aataggttag aaggtgatca caggaagcag agcaaggagc aataccctag gc

#atagaatg 141060

tttaagtcct gactactggc tgagacaatg gtaatgggaa gaaagcaaaa aa

#actaaaaa 141120

tggaaaaaat gaaaaacaaa aattatccag gattgattca cttgttcaac aa

#gtaattgt 141180

ggaacagtgt ctaatttcta ggagctatta tgaaaacttt gcctatatga ct

#tcatttga 141240

acctcacaag aaccttgtgg gacaagtatt atccctgctt tacaaacaat ca

#atctgagg 141300

ctccaacagg ttaaataatc ttctcaatat cacatataca ataaacggta aa

#tggggtaa 141360

acccaggacc attttgtctt aaagctcata aactttctga catattaaag ta

#aaaataat 141420

agcaaatgat tgcgatgatt ataactcctt aaaggtaggg actacgatat at

#gtctatgt 141480

atctccagta ggacttagca cagtaatctg tataaaataa tttcaaattg tt

#aaatcagt 141540

cagttgtcat aaggctgcct gctatgggcc aggtgcttgc ttaaaaaaaa tg

#aatgcata 141600

gacaggattc cttcatggaa cttatagtct gttgaaagaa tcagacatta aa

#tattacac 141660

aaaattacat tatacaaatg acgtaagtgc tatcatataa aagtatagga tg

#ccaagaca 141720

gtgagaaata tttccaaact tatatattta gaggctaagg agaggatatg tc

#tatttgaa 141780

tgaagataaa tttgagatga gaaaaagttt aagaatttaa tggagagagt at

#ttaaattt 141840

ttagtgttag ctaattgtgg tggtgtttta caaagctacg atgcatattt tt

#gaaaagct 141900

attttcctca taatatatta tggttatata cttagtgata tcttagaaaa gt

#ataagtac 141960

taagcaaacc tcttcaaata ataagctcaa aatatggaaa taggtgtatt ca

#taaaagga 142020

ttgtctctat attatttaaa tagtcatctt aatagtaaca atttaattaa at

#gattaata 142080

atccaagaat aagttatgtt gtatccctta caaataatgg ttctgaaggg ta

#atgtagca 142140

ataggaaaat gcttgcattc tagtgctatg taaaaaagga ataaaaatat tg

#tatgctca 142200

taaaaacatg ttgaaaatat acataagaac tactgaaaga agtataccaa aa

#atttgtag 142260

caattatggt agaaagacta tgagagatac ctttttcttt ttttattttg ta

#aatattct 142320

gtagtgtgat tttattatca ttgcaattaa aaatactttc tgaaatagaa aa

#agaataat 142380

cataaaaaca catttggctt ctatggatag atcctgattt tctgattgta tg

#ttttgtat 142440

taatacctga cttggtacat agcactctgg gagataatca agtcaataaa aa

#gacctgaa 142500

aaataaatga atcacaaacc ataactgttt agtgcacaca ggaaggtact at

#taataact 142560

acaaaggcaa aaggagagca tctgcaaccc aaggactaaa attagtaata at

#gttgaagg 142620

gagttctacc aaattatgtt ttccagaaga cagcgcaggc tcttcttgtg ta

#aggaagac 142680

agatcacctc cattagcctt gaaacaaaag caaagacttc tggatgaggg ca

#tttaatta 142740

taatgtttat gtaatcactc tgtagccatt tatataaaca agatcgctta ga

#gcacttgc 142800

ttttctgtgg gcagtaaagg gtactaaaag atgtatttta taaaaagtgt at

#tttaagcc 142860

aaataattca gcaccacaag tgaaaattat tggcatttta tactggtgtt tt

#taaacatg 142920

tagagaagtg cagatacaac cctttttctg ctttatgatt gttggacttt tc

#agtctatg 142980

agcttgtgat agtaacaata ataaataacc aaaatgagat acctaacaat ct

#ctatttac 143040

ttatgtcagg gcccattcta ggacttttat gtatattaat tcatttaatt tt

#ataataac 143100

ccctagaaag gacatgaact cagaagctgg aaaccatcat tctcagcaaa ct

#atcgcgag 143160

gacaaaaaac caaacactgc atgttctcac tcacaggtgg gaattgaaca at

#gagaacac 143220

atggacacag gaaggggaac atcacacacc ggggcctgtt gtggggtggg gg

#gagtgggg 143280

aaggatagca ttaggagata tacctaatgt taaatgatga gttaatgggt gc

#agcacacc 143340

aacatggcac atgtatacat atgtaacaaa cctgcacatt gtgcacatgt ac

#cctaaaac 143400

ttaaagtata ataataaaaa aaagaaaaaa aaataacccc atgaggttga tt

#attatcat 143460

tatcttcact ttatacataa ggaaactgaa acatagagtg attaaatggc tt

#gtccaagg 143520

ttgctcagct aaatgcttgg atttgaatga acataggaaa cctggctgga ga

#cctcagtg 143580

ttctaagcat acactatgct atgcatcaaa agaaacgttt tgcattaata ct

#ccatctta 143640

ttgccagagt cactagaaat tatttttgat gagattaaca aaaaagcttg tt

#ccagactc 143700

atattctatc tcctcacagt gctatttcca tgtttctttt ctctttcttt ct

#tctttttt 143760

ctttttcatt tatcttcttt aactttttgt agttttagaa ataagttcac ca

#atacagag 143820

gaagacagga aaatgggatt tttttctcac atttttcttg attgatttat tt

#agcatatc 143880

tatttttgat atgtaagaac ataagaagta agtagtcaga agtcttcttt ga

#gccaccaa 143940

gagttggtac ggagatatca aatgtcctta cacaactggg cagcctctga ga

#actgtctg 144000

ctgagatttt agatgtcaga ggtgcagact caagaaagaa caatatttgc tt

#gggtatac 144060

atgatatctg tgattttata catatataaa tacaaataaa tctttaactt at

#ttattttt 144120

aaatttgaat ttatttattt atgtcatata taaatcttgt atattaaaaa ca

#tattttcc 144180

actttggaat tgatttatag gtgagtaatg tcataaccta gagatagctt tg

#acagggag 144240

gcacgtaggt aactaacgtc cacttgtaga ctcaactctt caaaaaatgt ct

#ctcctatg 144300

acattggtac atcaaatttc taacttagca ttttcaaaaa gtcacggtta aa

#atgtaagt 144360

acactaccag gaatggagta acacatgcca ttgtattcac taacacagta ta

#accacttt 144420

ggaaagcaga gaccatgttc ttgagggagt agtaaagcaa aatgaatgga ga

#agccatat 144480

catcaggttt cgatggggtt ataggaaact ggacagtggg gctgaggaaa at

#gtggatgg 144540

tgtagttttc atgataggag ggcagagcta caggtgtttt ggaagaatac ct

#tataggag 144600

agaagtcttg aaagtggaag ctagcaaact acacggtgaa atgtagatta ct

#tcatttgt 144660

tctggagtca tctcactctt ctggctatct tgatagaaac agcaccaagt ca

#catattga 144720

ggcagcatac aatagctaaa agagtaggag tttccatctg gtcctggact ct

#ttttggtt 144780

ggtaagctat tgattattgt cacaatttca gagcctgtta ttggtctatt ca

#gagattca 144840

gcttcttcct ggtttagtct tgggagggtg tatgtgtcga ggaatttatc ca

#tttcttct 144900

agattttcta gtttatttgc gtagaggtgt ttgtagtatt ctctgatggt ag

#tttgtatt 144960

tctgtgggat cggtggtgat atatatcccc tttatcattt tttattgtgt ct

#atttgatt 145020

catctctctt ttcttcttta ttagtcttcc tagcggtcta tcaattttgt tg

#atcctttc 145080

aaaaaaccag ctcctggatt cattaacttt ttgaagggtt ttttatgtct ct

#atttccct 145140

cagttctgct ctgattttag ttatttcttg ccttctgcta gttttcgaag gt

#gtttgctc 145200

ttgcttttct ggttctttta attgtgatgt tagggtgtca attttggatc tt

#tcctcctt 145260

tctcttgtgg gcatttagtg ctataaactt ccctctacac actgctttga at

#gtgtccca 145320

gagattctgg tatgttgtgt ctttgttctc gttggtttca aagaacatct tt

#atttctgc 145380

cttcatttca ttatgtaccc agtagtcatt caggagcagg ttgttcagtt tc

#catatagt 145440

tgagcggttt tgagtgagtt tcttaatcct gagttctagt ttgattgcac tg

#tggtctga 145500

gagacagttt gttataattt ctgatctttt acatttgctg agaagagctt ta

#cttccaac 145560

tatgtggtca attttggaat aggtgtggtg tggtgctgaa aaaaatgtat at

#tctgttga 145620

tttggggtgg agagttctgt agatgtctat taggtccgct tggtgcagag ct

#gagttcaa 145680

ttcctgggta tccttgtcaa ctttctgtct cgttgatctg tctaatgttg ac

#agtgggat 145740

gttaaagtct cccattatta ttttgtggga gtctaagtct ctttgtaggt ca

#ctcaggac 145800

ttgctttatg aatctgggtg ctcctgtatt agatacatat atatttagga ta

#gttagctc 145860

ttcttgttga gttgatccct ttaccattat gtaatggcct tgtctctttt ga

#tctttgtt 145920

ggtttaaagt ctgttttatc agagactatg attgcaaccc ctgccttttt tt

#ggtttttt 145980

tttttttttt tttttttggt agatcttcct ccatcccttt attttgagcc ta

#tgtgtgtc 146040

tctgcacgtg tgatgggttt cctgaataca gcacactgat gggtcttgac tc

#tttatcca 146100

atttgccaat ctgtgtcttt taattagagc attcagccca tttaccttta ag

#gttaatat 146160

tgttatgtgt gaatttgatc ctgtcattat gatgttagct ggttattttg ct

#tgttactt 146220

gatgcagtta cttcctagca tcgatggtct ttacaatttg gcatgttttt gc

#agtggctg 146280

gtaccagttg ttcctctcca tgtttagtgc ttccttcagg agctctttta gg

#gcaggcct 146340

ggtggtgaca aaatctctca gcatttgctt gtctgtaaag tattttattt ct

#ccttcact 146400

tatgaagctt agtttggctg gatatgaaat tctgggttga aaattctttt ct

#ttaagaat 146460

gttgaatatt ggcccccact ctcttctggc ttgtagagtt tctgctgaga ga

#tccgctgt 146520

tagtctgatg ggcttccctt tgtgggtaac ccaacctttc tctctggctg cc

#cttaacat 146580

tttttccttc atttcaactt tggtgaatct gaaaattatg tgtcttggag tt

#ggtattct 146640

cgaggagtat ctttgtggtg ttctctgtat tttctgaatc tgaatgttgg cc

#tgccttgc 146700

tagattgggg aagttctcct ggataatatc ctgcggagtg ttttccaact tg

#gttccatt 146760

ctcccggtca ctttcaggta caccaatcgg acgtagattt gttcttttca ca

#tagtccca 146820

tatttcttgg aggctttgtt tgtttctttt tattcttttt tctctaaact tt

#ccttctca 146880

cttcatttca ttcatttcat cttccatcac tgataacctt tcttccagtt ga

#tcacatca 146940

gctcctgtgg cttctgcatt ctttacgtag ttctcaagcc ttggtttcag ct

#ccatcagc 147000

tcctttaagc acttctctgt attggttatt tcaggacata ggcatgggca ag

#gacttcat 147060

gtctaaaaca ccaaaagcaa tggcaacaaa agccaaaatt gacaaatggg at

#ctaattaa 147120

actgaagagc ttctgcacag taaaagaaac taccatcaga gtgaacaggc aa

#cctacaaa 147180

atgggagaaa attttcgcaa cctactcatc tgacaaaggg ctaatatcca ga

#acctacaa 147240

tgaactcaaa caaatataca agaaaaaaac aaacaacccc atcaaaaagt gg

#gcaaagga 147300

catgaacaga cacttcttaa aagaagacat ttatacagcc aaaaaacaca tg

#aaaaaatg 147360

ctcaccatca ctggccatca gagaaatgca aatcaaaacc acaatgagat ac

#catctcac 147420

accacttaga atggcaatca ttaaaaagtc aggaaacaac aggtgctgga ga

#ggatgtgg 147480

agaaatagaa acacttttac actgttggtg ggactgtaaa ctagttcaac ca

#ttgtggaa 147540

gtcagtgtgg cgattcctca gggatctaga actagaaata ccatttgacc ca

#gccatccc 147600

attactgggt atatacccaa aggactataa atcatgctgc tataaagaca ca

#tgcacacg 147660

tatgtttatt gtggcattat tcacaatagc aaagacttgg aaccaaccca aa

#tgtccaac 147720

agtgatagac tggattaaga aaatgtggca catatacacc atggaatact at

#gcagccat 147780

aaaaaatgat gagttcatgt cctttgtagg gacatggatg aaattggaaa tc

#atcattct 147840

cagtaaacta tcgcaagaac aaaaaaccaa acacggcata ttctcactca ta

#ggcgggaa 147900

ttgaacaatg agaacacatg gacacaggaa ggggaacatc acactctggg ga

#ctgttgtg 147960

gggtgggggg cggggggagg gatagcttta ggagatatac ctaatgctaa at

#gacgagtt 148020

aatgggtgca gcacaccagc atggcacatg tatacatatg taactaacct gc

#acattgtg 148080

tacatgtacc ctaaaactta aagtataata ataacagaat aaaaaaagta ta

#atatataa 148140

taaaaatatc ttgaaaatta aaaaaaaaaa caaacttctc aatggctgtc cc

#tctcattc 148200

aagagcaaaa ataaaatcat aacaatcctt gaaagcaaaa aaaaaaaaaa aa

#aaagtagg 148260

agtttcaggt tgggacagac ctggattcaa gtttatttct atcagtgtag cc

#ttggataa 148320

gttatcaaac atttagttcc tcccatctat aaaatgtagc aattaaacta tt

#aaactaga 148380

aaatccacta tatgccatgc gtatagcaac tgtatgcacg ccatacctat ag

#gcatagat 148440

atacagtagc tacagaaaac atatatgtat gtatatacac atatacattt gt

#acatggag 148500

gtattcacat atctacgata gtgctatctt tctccctcgt tatgttactt ct

#gcaagaaa 148560

cttgccatat tttctctatt ttatattttt gtttcttatg tatggattta ct

#tttaacaa 148620

attttcaaaa tatgcaaata actttctgtt aaactatagt actggccctt tt

#atttctga 148680

ggtaaactaa ctgaccatct tagggaattc tatttgttag caaccaaaaa aa

#aaggatgt 148740

ttgccactta ataaacagat tcagacaata tattactaat ttacttcaac ga

#gaaagaga 148800

ctcttgcttc tagtgaatga tattacacag tttgttttgt tttgttgata gc

#actactgt 148860

gcaatggtca cctgtgatac aattatttga attcatgaca atgctgggtt ag

#gaaccgag 148920

gcagatccac tatgcttctt tatgttcaga tgttttaaat cagaattata gg

#actatatc 148980

tatgtgccta ggcaaatatc taaaataatt attccattct ctgctaacag ct

#taaacacg 149040

tgttgtaatt ctaacagact ttagagagca tatggcagtt tcaacaagtc ac

#acatattt 149100

ttacatgcac ctaagctagg gacccctgac caatgagttg agcatcatct at

#caggatgc 149160

tcccgataga tgacagatct tcaaccagcc agctaggtca tttctgcttc ct

#caattcca 149220

catgtttagt tagttgggat tcccagtcgg gaggcaaagc aggtagcatt tg

#ggccctcc 149280

ccttactgtg ctcagttcag tttattgatg gaaacatctc caaggatctt aa

#aactttaa 149340

aatagaaaat atctcttcct cacaaagttg gaagccctga acctgagcct ta

#agagattt 149400

atttttacat ttgttttcaa attctcacaa tttatacaga aaaaaaaatc ag

#agtatcca 149460

ttctggtttt taattttttt atttcttgcc atagtattat atatcaagaa ta

#tttataag 149520

aaggaagtag ttaatacata tttgttatct aagtataatt tgggacacta ta

#taaatctt 149580

ttagtttgtg agttacttct gtaccctgtc atctcctaag ctacctggtc tt

#tcttggaa 149640

taataaatat acataccttt taggaccaag atctatagtt tcacaatatt ca

#tagccatc 149700

tggttctgct acagggtaaa tttagactgg aaataaggta atattaagta ag

#agaagctt 149760

cgtttgttta acctacctcc caaaggctcc atttgtaaag agtgcagacc ag

#aaatcaca 149820

tgcactgctg gattctttcc atgagaaaag cctgtgttga gctttagttt ct

#tcattttc 149880

tttaaacaga acaaaaatct ctcctaccac tcaaaggagt gatttgcaga tt

#taatgcaa 149940

ttatatcaaa gtagtttata acccataaaa cacaaagtta tatgaccgtt ac

#tttgtatt 150000

gaacatccat gaaactctag gaatagtact agaagcttta tacaccatta ta

#tatagaat 150060

ggtgtctctt ttaattctca agaaatcctg tccagttgtt ataattatac tt

#actgaata 150120

aattatatta atttatatta taattatatt aattagttat ataatgaatt ca

#tagaaact 150180

caggggttgg gtgatttgct aagatcaata gctagaaagg ggcagaatca gt

#attcaact 150240

caatattacc tccaaatgga agtaattcag tattagtgag tattactaat ta

#tagaagta 150300

atacttctcc tttctactca gagctaacac aacagcatta tctaatgttg tt

#aaatggta 150360

ggtggaatta aaaattgtag gtaagattaa gaaaggaggg aaatcactga at

#aacctgcc 150420

cttccagcaa agttgacaaa gtagataaga tctctggtaa gatctaatct tc

#atctcatt 150480

ctgccacatg tttttgtttt gttttgtttt gttttgtttt gttttatttt gt

#tttttaag 150540

acgcgtctcg ctctgtggcc caagctgaag tgcagtggca caatcttggc tc

#actgcaac 150600

ctctgcttcc cagttcaaac aattctcctg cctcggcctc ctgagtagct gg

#gattacag 150660

gcgtgcacca ccacgcctgg ctaatttttg tattttcagc agaaaggggg tt

#tcaccata 150720

ttggccaggc tagtctcccc atgtttttta tcgaagtccc tgtgttctca at

#atcctgag 150780

atgattggct gattggctgt tgccacagcc attggcttca gccactcttc tg

#gcctggac 150840

atcatccagt gcatgtcaaa gacaggactc tggcctagct tcttttgggg ac

#tttctacc 150900

acagaatgag caaaggtgat gttcggaaca aaatacctat acgtttcatc ca

#gctgcaaa 150960

taatcagctc cagcttctgg agttacttgg tacctaaatt ggccaggttg ct

#gttgagga 151020

tgaatgggcc aatcttacag ctgaacacca tgatactggt tcccaggagc ca

#agcattgc 151080

cccaatccag ccttttttta tttattttaa aaatgtgtta atacttttta aa

#tctttaag 151140

tagtgactaa ttttctttta aataaagatt gttttcctcc aggatgcatc ag

#agtaaaag 151200

cataaaatgg agctttaaaa aaattaattt agaatcagtt gtgtcttcag tt

#tactaatc 151260

cacgcttcaa atgagtagaa cttacaattt gctctggttt tgttacttgg gt

#gggtaaga 151320

taacttagaa gagcgacagg gattttgcta aaatataaaa atgggatagt tt

#taaatctc 151380

tattgttgtt accgttggca gtaatataaa ggagatcaaa gaactaatgt gt

#ttgttccc 151440

aacctacctt taaataaaat tgttttatag atgttataaa agtataccta ta

#tacacttt 151500

atgtacacac acatgcattt catgtatata tccactataa tgctagttct ct

#cttattat 151560

aacactcctg caagaaattt gccatatttt ccctattttg tgttttagtt tc

#ctttttgt 151620

cattaataaa tatactaggt tttcagagta tgaaaatgtt ttcccatcaa ac

#tcttatgg 151680

tgttgggcct tttttttctg agataaagta acagagaaat caatttggga ga

#atcttctc 151740

attaagggag catactactc cttactagtg aactggctta cagactgagg tt

#ggcaggtt 151800

cagatatgta tgagcagaac agtagcaaga catttgcaga cctatgatcc tt

#gcttgttc 151860

acctaattct ttttacctaa cactgccact actgtaaaac caaagcaaga ca

#ttcagaaa 151920

aagacattgc agaccaaatt gacactttga gggaggctac catgggtata at

#gtataagc 151980

ctccatttgg agcaggatcc aagatcaata tggatacatt agattctact tt

#ttaaaata 152040

agcactcatc tcatttcaga ctatggacat gctactgagc tttactatcc tt

#aatcctta 152100

gtctagtacc tcggtatctt cattaagtat gaaaggttat ttctattagg ac

#ttgcctct 152160

gagtcccaaa ctgggactca ggatcagatc atggaggaac atgaaactct ta

#tgtggatg 152220

atgacatgga ttgggcatct gtggtggttc tggaacttca ggattcacct ga

#tctgcctc 152280

ctacttatct ttggaaaaat gtaaagtata ggatctttct accacaatct tt

#actactgt 152340

agggagtttg atccactgac tcttttcaaa agacctctca gtgttcaagt ac

#ttttcttt 152400

aatgccattt cttgagagtt ggagctacag ttgctctaga tgtgtctagg tc

#tgatcttt 152460

tctccccata ctccttgagc ccctgataac caccattcta ctttctattt cc

#atgagttc 152520

agtcttttta gattccccat ataagtgaga tcacaaggta ttggtctttc tg

#tgcctggc 152580

ttattccact taacataatg tccttgaaat tcatccaaat tgtcaaaatg ac

#agaatttt 152640

gttccttttt aaggctgaaa agtattccac aatgtatata tgccacttat ct

#ttctttct 152700

ctttctttcc tgcctgtttt tctttctttt cttctttctt tcctctttct tt

#ctctttcc 152760

ccttccttct tttctttctt tctttctttc tttctttctt tctttctttc tt

#tctttctt 152820

tctttctttc tttctttctt ctttctttct ccttccttcc tttctttttc tt

#tctctttc 152880

tttgtttctt ttttctttat ttctctctct tttctctttt ttctttctat tc

#ttttcttt 152940

ctctttctct ctctttctct ctttgtttct cccttccctt cccttccctt tc

#ctctttct 153000

tttacaggct ctcactctgt cacccagtga gtacagtggc acaatcatag ct

#cactgcag 153060

cctggaactc ctgggctcaa gcaatacttc tgcctcagcc tcccgagtaa ct

#aggacaac 153120

atgcacatgc caccacatct gcctaattta aaaaatttgt tatagagaca ac

#attcttgc 153180

tatgttgccc agattgttct caaaggtctg gcttcaagca atcctcctgc ct

#tggcctcc 153240

caaaatgcag ggattacagg catgagcccc cacactcagc ctcaatgcca tg

#tttgactt 153300

atcctttcgt ccattgatgg gcacttaggt tgattccata tcttggctac tg

#tgaataaa 153360

tgctacagtg aacatgggaa tgcagatatc tcttccattt actgatttaa tt

#acctttgg 153420

gtacatatcc agtagtggaa ttgatggatc atatggtagg tctattaatt tt

#ttgaagaa 153480

actccgtact gttttccata tggctgtact aatttatatt cccatcaaca at

#gtgaaaag 153540

tttccctttc tccacctcct cgccaacact tgttcagaca ctttcatctt ta

#aaaaaaaa 153600

ttaattttta attttgtgca cacagtaagt gtgtatatgt atggggtgca tg

#agatattt 153660

tgataccggc attttgatgt gtaatgatca catcagagta aatgagatat cc

#attacctc 153720

aagcgtttgt tctttctttc tgttacaaac aatccaattt tgctctttaa at

#tattttaa 153780

aatgttcaat ccattattgt tgactgtagt caccctgttg tgttatcaaa ta

#ccagatct 153840

tattcattct acctaactat atttttgtac ccattaacca cccccacttg cc

#tgcccacc 153900

cctcattacc cttcccagcc tctgataacc atcattatac tttttatcta ca

#tgaggtcg 153960

attattttaa tttttagctc ccacaaataa gtgaaaacat gcaaagtctg tc

#tttcagtg 154020

cctggcttat ttcacttaat ataacgacct tcacttctat tcatgttgac ac

#aaatgaca 154080

ggatctcatt ctttttatgg ctgaatagta tttcatcata tatatgtacc ac

#attttcct 154140

tattcattca tctgttggtg aatacttagg ttgcttcgaa atcttggcta ct

#gtgagtag 154200

ttttcatctt ttcgataata accattctta tagatgtgag gtagtatctc tg

#tggtttta 154260

atttgcattt ctctgatcat tggtgatttg agcatttttt cacataccat tg

#gctatttg 154320

tatgtcttct tttgagaaat gtctattcag atactttgcc catttttaac ct

#tgtttttt 154380

ttcttacagt tgtgttgagt tcctcgtata ttttaaacat taatctctta tc

#agatttat 154440

ggtttgtaaa tattttatct cattccatag gttgtatatt cactctgctg at

#tattttct 154500

tggctatgca gctttttagt ttgatgtaat ctcatttgtc tatctttgct tt

#cccagtct 154560

gtgatttggg gttaaatcca aaaaaaaatt atgcagacaa atggcaatgt tt

#tcttatag 154620

tggttttagg tatttaatcc ttttttaaat atggtgtgag ataagggtct ga

#tttcattc 154680

ttccacatgt ggatattcag ttgtcccaac accatttgtt gaagagactg tc

#ctttcccc 154740

actgtgtgct ctcagcatct ttgtcgaaaa tcatttgacc ttaaatacat gg

#atttattt 154800

cgggttgtct attctgttca ctggcctctg tgtctatttt tatgccagtg cc

#atgctgcc 154860

ttgtaataca gctttgtggt gtattttgaa gtttgatatt gtgatacttc ca

#ggtttgtt 154920

ctttttgctc aagatttatt tggttatttg ttttttgtgg ttatacaaag tt

#taggattg 154980

cttttttcta tttttgtaaa aaatgtcatt ggcattttgg cagggattat at

#tgaatctg 155040

ttgatagctt ttgttagtat ggatatttta aatatcagtt cttccaatcc at

#aaacacag 155100

gatatttttc cttttatatg tgtcctctac aattatttca tcaatgtttt at

#agttttca 155160

gtgtacaggt ctttcacctc ctttggatta aatttattcc taagtatttg aa

#atttattt 155220

tggtaactat tgcaaacagg attgttttct tgattttatt tttcagatag tt

#tgttgtta 155280

gggtgttaaa gtgctaccca tttttatgtg caaataagga taattttctt tc

#tttctttc 155340

tttccaattt ggatgccttt tatttctttc ttttgcctaa tggctatgac ta

#gaacttcc 155400

agtacaatgt tgactaaaag tggcaagagt aggcattctt gtcttattcc tg

#atcttgca 155460

ggaaaacctt tcaacttttc accattgaat aagatattag ctgtgggttt at

#cacatgtg 155520

gtctttattg tgttggggta cattccttct atgtttaatt tctgagagtt tc

#tatcatga 155580

aagaatgttg aattttgtca aatgcttttt ctgtgtctgt agagatgatc ac

#atggtttt 155640

tgttctttat tatattaatg tagtgtatca catttataga ttcgtaaatg tt

#gaatcatc 155700

cttgcatctt tgggatatat ctcacttgat catgatgaat tattctttta ct

#gtgttgtt 155760

gcatttaatt tgctggtata ttttgaaggt ttttgcattt atgttcatca gg

#gatattga 155820

cctataatat tttcttgtaa tgttcttgtc tggctttggt atcattgtaa tg

#ctttcctc 155880

ataaaatgag tttggatgta cttctcttct tcaatttttt gaaagagttt ca

#gaggaact 155940

ggtattatta gttcttcatt aaatggttga tgatttcagc actgaagcca tc

#aggtcgtg 156000

ggcttttctt tcttgggaga ggcttttggt aattgattca atctccttac tt

#attattgg 156060

tctgttcaga tcttctattt cttcctgatt caaccttagt aggttatatg tg

#tctaggaa 156120

tttatccatt tttttctagg ttattcaata tgttggataa taattgttta ta

#gcgttctt 156180

ttataatcct ttgcatttct gtagtgtatt ttaatgtctc ctctttcatt tc

#tgatttta 156240

tttgtttgaa ttttctttcc tttattcttg gtctagctca acatttgttg at

#tttgttat 156300

tatttcaaaa caccaacctt tagttgagct gttctattgt tagatagaat ag

#aatagaat 156360

gttctatttc aacaataaaa tgttgagcag ttctattgtt tttctacttt gt

#atttcact 156420

tatttctgct ctgattatta ttttcctcct tttagtaact ctgtgcttag tt

#tcttctta 156480

ttttgtgtgt cttaaggtac aatgttatag gttgtttgag atctttctcc ct

#ttttgatg 156540

taagtgttta ttgccatgaa ctttcctctt agaactctta ctgttgcaat ct

#acaaaagt 156600

atttgttttt ggcaagttgt gtttccattt tcatttgtct caatacattg tt

#aaatttat 156660

cttttaactt cctcattgtc ccactggttg ttgaggagta tgttgtttaa tt

#tccacata 156720

tttctgcatt ttccaaaatt cttcctgtta ttgatttcta gtcgcatacc at

#tgtgttaa 156780

aaaaaagata ctcaatatgg tttaaagtat catttcagtt aatgatctgg ac

#cttaaatg 156840

atggcagcat aatcaatgtt aatcacaaac caaaggctat ttagtgttat ta

#ttttaata 156900

tgcaatatac ttaccaggcc ccccagcact cagtctgcac agtctagacc ct

#gcctatct 156960

cagatccata ccccatctct tcctccaccc cttctgtttc aaccaaatta ac

#actgttta 157020

ttctctgtag ttccccaccc tcactgccgt gcccacacta tgtcttacca aa

#ttctgtcc 157080

ctcttttaga tctcagtttt ccttgaacac ccagactcaa ggtgtggatg cc

#tatttgtt 157140

tatcttttta gtagcccaga cttttttata gtacatttta cagatgtagt ca

#aataattg 157200

tgtaattggc tacttaagat ttctctcctg catttaaaga aagccccgag at

#tatatcta 157260

tcttgtccaa cttagcatgc tgtcttgcat gacaatcatt aactttttat tg

#agttaatt 157320

aagcattgtg cagaatgcct agatgcctaa gctttcaatg ttaccaaaca tg

#tggaacaa 157380

aacttactgc aatctaggtt cccctgaaaa catagcctaa ggtggaggct ta

#cttgaagg 157440

ttaccgtacc ttaaggagga gaagtaaaga acaggaagtt actgttatag ag

#tgaatttt 157500

tctccatacc ccacccaaat tcatatgctg aagccctgtt gactaaagaa aa

#aaaaaatc 157560

aagcttttaa agtatcaggc caggtacggt ggctcatgcc tataatccca gc

#actttggg 157620

aggctgaagc aggcagattg ctttaggcca ggagttagag gccagctggc aa

#catgacaa 157680

aaccccgtct gtactaaaaa tacaaaaatt agccaggcac gatggcgatc at

#ctgcagtc 157740

ctagctattc gggaggctga ggcacgagaa tcgcttgaac ctgggaggcg ga

#ggttgcag 157800

tgaaccgaga tcatgccatt gcactccagt ctgggggaca gagagaaacc ct

#gtctccaa 157860

ataaataaat taattaatga attaattaaa taaagaaaag ttagctttat tt

#ggaagtct 157920

gaggactatg gaccaaggcc tattgcctgg gatcagttct gttagaccat tc

#caatgcag 157980

caattgagtt cacagtttgt atacaaatgg tgaggattca ttacatgcaa aa

#tcacatcc 158040

gagttcgtgt ataagagttg atatttatag attattatta ttatagatta ta

#ttatagat 158100

tatacattat tatcgataat aatctattat cgataataat aatctataac ct

#ataacatg 158160

ctaggctgcc ttctgctgtt gaaaataatc caaatatctt gggcatataa tt

#atcattga 158220

gaagggcatg atatgtacaa gagaagtatt caactggttt ccccatgatc gc

#aaaccttt 158280

ggagcttata gaagagaaaa aaaaaaaaga gagacaaagc aaatataaaa ga

#gattttga 158340

gataatttgt acactctgaa atgagaaagc aaacttaggg ctgacacaag aa

#gaactaat 158400

tatttttttc aagtacattt tattgttatc aaaatagtcc atacatatcc ta

#gggaaaaa 158460

aaaccccaca aatagtacag gaagattata atttaaagca ccagttcact ca

#aaggcaac 158520

atttttaaca aaatttttta aaattatttt tagtgatccc tctaaatttc ta

#aataatat 158580

gcttatattt ttttcttgtt ttacccatgt taagtgtgac aaatttactt tt

#tgctctta 158640

taaatatgga tttagctaat tttattttta ttttatttta ttgagaccag tc

#tcgctctg 158700

tcgccaggca gagtgtgcag tgatgcaatc tctgctcact gcaacctctg tc

#tcccaggt 158760

tcaagtgatt ctcctgcctc agcctcctca gtacctggga gtacaggcac tt

#gccaccat 158820

gcctccctaa tttttgtgtt tttagtagag atggggtttc accatgttgg cc

#aggatggt 158880

ctcgatctct tgaccttgtg atctgcctgc ctctgcctcc caaagtgctg ga

#attacaga 158940

tgtgagccac tgcacctgtc cagatttagc taattttcta cacttatccc ca

#accttcct 159000

cttcactcta cctccctttt caatacgata atatcacatc ttaagttcca tc

#atccctgt 159060

aacctctgta gctataagta tatagccaca attaacatat gtagatttcc at

#ttctgatt 159120

ctatcagcca taggtaactg tctttacatt ccactttgta agaggagatg aa

#taattctc 159180

acctttcctc ccaactctgt gttcctcctt ctacctcccc acccccaact cc

#gttgtagc 159240

ggctattaac atatattatt ttgtaaccat gggtaagtgt taagtaattt gc

#ctaaagat 159300

tgattctaaa aaatttaaaa atatagaaat ctataaaatt ctgtaaattt ta

#gattttct 159360

ataattatag aatgtaaaaa tatagatttt ctataaacat agaatgtaaa at

#tctataaa 159420

aatatagaaa tctttatgta attataactg tgtaagtatt atttactgta ga

#accaagta 159480

atgtgcaatg cttccttctc catggctcca gtgtcatgac atctatagta ct

#ttacaaat 159540

aatgttatga gtatatactt ccagaatggt ggtaaaagaa gctctgcaga cc

#ctctcccc 159600

agtgaaacaa ccatactggt aaaagtaatt ttaaaaggca atcatgaaaa gt

#ctctggaa 159660

attttcttaa gggtatacag caaatgaaga aacatttatt ccaaaaagtg ta

#ctaaatct 159720

tggtaagaac aatgagtcca aggcacctaa gtcacaaccc acttcccttc ct

#ctcctccc 159780

agctcagcat gacagaagct taactctgga caagaacaca gggcttcctc ag

#cttccagt 159840

tgaggccaac tgtatgttcc caagaggaga agaccaacag cgtttcttgt ct

#cccttcac 159900

ccttcccctc cagaagctaa attctggcta gatgaatcca agatattggg gc

#tcccttct 159960

ctcacccagc tcctactggt agggtggagg ttcaacctca ggcctggaac ac

#tgagaata 160020

gtatgggttc ccaattatta atgagactct gattattgcc catgctcagc tc

#cctgctcc 160080

tacagcagag gagtcactta cagagaaaca caatgctgtc cccatcccta gc

#tctgaagc 160140

cgcgcgtcag agattttccc cagtgggagc actgaagctc tttgcaaagg aa

#ctgacttt 160200

atttgaagca gagtaaaggg aagttcaaga taaaggtatt ctcaaaaata at

#gtaagttc 160260

tggtggaaag caattaaggg gaggttggta gcttcgtgaa agagacaagc ta

#aaccagat 160320

tagctagtgt atgagagaga atcaggaaaa gagatagcta agaagagccc tc

#ctgggtca 160380

gaacaaacct caagcactga ccacagcagg cagggcactg tggcttacac ct

#gtaatccc 160440

agccctttgg gaggctgagg tgggaggatt acttgagcgc aggagtttga ga

#ttagcctg 160500

ggcaacataa caagactctg tctatatttt aaaaacaaaa aacaaaaggc ta

#ccacagca 160560

aaaaggctgg aatttagttg gagcagaccc ccagagcaat ttatgtccca gg

#acattgta 160620

aaaaataaca gaacaatcta gaacagaata gctgggtata tgtgataagc ct

#tagagcaa 160680

ccactaagaa aataactcga aaaatacata gtgaaggaaa gaaaacaaca at

#gttcctaa 160740

catcacaatc aaatgaattc tccttttcaa catttcacca gaggctcaaa at

#cattccac 160800

gtttaaaatt tttttctctt tataatgtct actgaaaaag tagcaaaatc ta

#ctgaggag 160860

agctttattt ctaaaaggga gtatcacaac ctgcaagtgg gaaatggagc ct

#ctggttaa 160920

aactgaaaag caggtgcttc gaaggaggaa aaatgagaca ggaattcata ct

#aaatggat 160980

tggtttagca tacatattca accggctatt ggaggagcta tgaatattca tg

#aaggggca 161040

cacgtgtagt aagctaacat gtctattaca tatgtcccat gttcactttg gg

#gtggaaaa 161100

agcatttaaa tatactaaaa ttaagctcta tatgtcaaaa ggttaagcag ag

#gacatgaa 161160

gggactcagc atacagtctc tgtaaactgg ccagaaccac tccatgttca gt

#gttctctt 161220

attgggaagg aatgctagcc agttgctgtg tcgaaactac aaaaagcaag gg

#gcagcgta 161280

acatggttgg ttgaaatcag ccatggagca agtctttcaa aagagcttgt tt

#ctgtttaa 161340

cccttaggaa cgaaagccta ctggtggtta acaaggtagg gggtgttaca gg

#gtgtggct 161400

gacctactgt tccatcatag acaggagctc agtttttaag gtttctctgg gg

#tctccaag 161460

tgagcctccc tggagaatcc tccaatttcc ctagtgagag caagaaccat at

#ctgtctat 161520

actgcccaac tcagttgttt ttgcaataat agacaataac tctttaaaga at

#gaataagt 161580

ggtggtgaaa tgaaacagag taagttcctg atgtagaagg cagaagggag ac

#tgttgctt 161640

aggcagacca agtagaaact atacgatatt ttctatagta ataaccttag aa

#atggcaat 161700

tcggttctat agttcaatta atatcactaa aagagctgtc caatgaactt ac

#aagttatg 161760

tggtatatgt gggttaatct gggagaccaa ccaccattta tgaaattctt ct

#ctatgaaa 161820

atgctttatg aagggcaaat agcaagttta caaatgaatt tttggaaaac aa

#actgtaaa 161880

ttgaggttaa cttctaaggc tgttaatttg tgggtatctt tgtctatatc tt

#cttctcac 161940

tgatatatcc tcaggtagct agagttctcc tttcaactag ccttaatttt ga

#attatatg 162000

ccagttataa atcatcttca gaatatgaat taaatacccc tttaatttta at

#tgatatga 162060

ttttacaata ttaactacat agtaacaatg gatttggata tttatcattt tt

#ctatttga 162120

tttataattt agggccaaat gggtgtcata aggggctctc attccaggaa ac

#actgtaga 162180

gtagtctagt atcctaacag tctatccatc ttgatttttg aaaatagtct gt

#tgtggagt 162240

agtttaggat aacctaacta cttgtctgtc aaatagagga atgctgtgac tg

#gagaaaat 162300

ggagccgtta tacattagtc ttcggtacag tcacaaaaag ctacttattt ca

#caaaagac 162360

actattttgc cttttcaggt gtaactgtgt ggaaccgcat aatcccagca at

#ggcacatt 162420

gaaggaatgg agggaatcca atatttctgc ctctgacata atttgggaga ac

#ctaactgt 162480

gtcagtaagt aaaacactga aaaataagtc atacctaaga gcttttgttg ac

#attttgac 162540

tcaattattg ccattacagt aaaatttttt tgaatgcata atataaaact aa

#tagttgtg 162600

ttttaatttt aatttcatca tttcagatgc tcatcagtaa actggggtta tc

#tttcatta 162660

ttaaggttgt tctaatagaa gaccagaatt gctcaaatag ctcacttata ca

#gaaatatg 162720

tgaccgagat ggactgaaag cacattaaat atgagtggtg ttgacctaaa tg

#aaaccata 162780

tggcagaact aagtctgcct tctgtgtaaa gaactcagaa tgctcttact tt

#actctgta 162840

atgctgctcc agctgttccg gatctgctgg ggggaaaggg atgtttctaa ta

#ttctagtg 162900

tcaatactaa agtctttggg aggaacaaat atcacttttc ttcacaaaat tc

#tggcacct 162960

ccctcaacaa gatctttctt ttttccattt tattcttatc tcccactcaa ga

#aagagcat 163020

ggcaacatat ttttcaccta taacagttca atcctgtgcc attgtcttat tt

#cctttgac 163080

ttttctctac tttgtgattt cttttttctc atacctgcat ttctctattt tt

#ctgaatct 163140

attctgtgcc tcctttccta tcaatacttg cattctatgc ttctggttca at

#aaaatctt 163200

gtaatttgaa aatgtgttct actttaaata aatattaaaa tctgagtagc cc

#tactttct 163260

tttctattct tcccagctat aaacattaca ggttcaaacc ttctaccact tt

#acctaccc 163320

atataggctc aagttttatt atgactatca gcacaaaact attgagttct ag

#ttcatttg 163380

atcaaatgca tactatttta gtaagttgtc tagttagtga gcatagaaat ct

#tttttggt 163440

gtacagatgc tataaaactc taaacatgat tcttgtaaag agcatatgat ct

#attgacta 163500

tattcttgat tttctctatt gaatatgttc tttcaaaatt gaaatcaaat ta

#cttactct 163560

ttatttaaaa ttctatcttg acctatattt tactacttct attcttaccc ta

#gctgtgtt 163620

ctgtagaata agccttcagt tactcttatt gttttctttt gttattgtta ac

#atttattc 163680

tgttccacct atttttccct agaaaaataa cattgccagt ctgcttccac tc

#aaagagcc 163740

atttaaactg aacaataaaa gaattgatga gctgatcaag aaaaaacact at

#agttattc 163800

agaatttaga catggggtca tgattaatga aatcattagt gggtcttctg tc

#tacacttt 163860

ctttggtaaa ctatattatg tttacagagc ctcttgatgt cttcttcaat at

#gaaaaccc 163920

aaatgatccc atctctaagt tatataacat gataatttac tctatatgtg tt

#ttgtatta 163980

tgtgaataat ttaatactaa ataataatat tccttctatg tattagcaaa tc

#ttgaattt 164040

tgagagttct aagaagcaga catacagcac agttatcagg ctagctgtga gt

#tagatacc 164100

ctgagttttg aggtcaagta gaatagtgaa aaatattttg caattaaagc aa

#atacagca 164160

ttgtggggtt gttggttttt ttctcttttt ttttgtcatt ttaaaaagtt tt

#gtactagg 164220

tgttaacatt tgagcagaaa gtttcatatt atttttcatt agttaaaagc ag

#tttttgca 164280

atggataatt gctaaacttg accagaaaca gtctttatca ccagagggaa ta

#ctatataa 164340

tgaaaacaat cttgtaattt ttaagtcaaa aaaagaccat taaaattttt gt

#ctaattgt 164400

tatgctgaat tttttcctca atatattcat aatgtcatca aaaatatttt at

#taataaag 164460

cactgaacta gtggctatca caactaattt tgttaaaata gtgacataac at

#ttaattta 164520

catattattt gtttggcagg tcctgtaatg ttttattgag ttgtttgtta ca

#tatctcat 164580

gaattataat ttataccttg ccaactcagc aagggcaaag aactttagtt tt

#ctctgatt 164640

ctcccaaact gctctatgca tagtaagtgt caaacatttg atagaagtac tt

#aatgtctg 164700

tttgaaacag tttcatctta ctatttaatg caaatattta tggcaaactg ga

#gtacttaa 164760

gtttgtgtgt atatatatat atatatatat atatatatat atatctctct ac

#atatatat 164820

gcgtgtcgat atcgcgaaaa accgtctcta tatgatactc tcgcgcaacg tc

#gaagagta 164880

agcaggcgca gctcaaccag cacgaggtgt cgcagtcact acctcgcata cc

#ttgcgtgt 164940

nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn ta

#tactatag 165000

gagccaagta gcaaagcata tgtatgacac gcaggatcga ctctacgagg at

#ccccctta 165060

ggcaagattt aaaatattca taagcagtta accagcattt ggtgtttcag tg

#cctgaatt 165120

acatatttag cttgtacata tataaggggc aggacactaa tgccaacttt aa

#tttcttat 165180

tctaacttaa tttttgccaa cttatagaat tgctgaaact tagaatgtgt tt

#gaagagta 165240

attagtagaa atcagtttgt caacaagcat tttttgagta cccattgtaa ct

#gaaaccat 165300

atgttagact caaaaaacga gagcaggatt tggatttggt tttcatttct aa

#atttcagg 165360

acttactctg tgtgtatgtg tgcatgtatg tatgtgtgca tgtgtgagtg cc

#tctgtgtg 165420

tgtattgggg atacaattag tataaatctg aaaataattg ttgaatttag ca

#ggtcacaa 165480

tttttctctt ttaaaattag cattttgttt cctcccaaag agaaaataaa ta

#acattttc 165540

aaatatgctt tgaattaatg taattaggca gaccattggc aaattataga gt

#gtaagaca 165600

gctaaggaac cctttaaatg tcatctatgt tcttaagaat tgagaacaag at

#cccgccaa 165660

atgactttta tacctgcaga aatgacaaaa gatgctcaca aatttataga ta

#atgtgttt 165720

atcatggaac ttttagctcc tttttctatg tagcaatttt gctacccatt at

#attgctta 165780

ataattgctc tgctagcatt tctggacagg tgcagaagag gatgaaaaac ac

#aaggattc 165840

atttttgcca ccttatctat ttttaaagca ttttgaaaga aggaaaatta aa

#actttaat 165900

taaggcctgg gggatttttc tgtggttttt caattagcca agttgctgtg ct

#ctgtatta 165960

gcttaacatg aataattgga atttaacttt gcctatcaag gaagatgttt gc

#agttaaat 166020

tagaaaagga gacagattct ttaagacaat aataaggtgt attaactata tt

#tctcaaga 166080

ctctcaggct tagggtagct agcaactcca agtagatttt actagttgtt tg

#ttttcaga 166140

tgacagtgta gctatttgta atttattcta caatctttgg agtgtattta ct

#ttttgctc 166200

tacaaagatt tcaggcctaa agttgggcag actctgtgtt tgtgatcaat ct

#atcagttc 166260

atatttgtct ccaagatctc tctgcaattc aatttatgtt cagggcaaga at

#atctcaag 166320

gactaatgag atcactggat catttaaacc attatttcct gttttgaaat gt

#aaaaatac 166380

tttagtaatc taatttttaa ataagataaa ccaaagtaag tttaaaataa ct

#ttttttca 166440

ttcaaaatat ttgtttgaaa tgctcagttt ttcctggagg aaaaaaattt tt

#ttgacttt 166500

gctgccacct catggctaag gcagtaatta gaaatagttc ttcaggctct ta

#cagaacta 166560

cagttgcaga agaaaaaata atccatggag aagtcatagt aaatatgagc tt

#tgccttgc 166620

tcatgtagta attttatttc atttgttctt tagtccaagt tcgatagtcc ca

#tctttgac 166680

ttacaagttc atttcagtca ttgtatgtca tagttttctt gttgcctttc tc

#atctttct 166740

tggcagcttt tggactagat aattctacaa agtcattgtt cttagtcaat aa

#gcaataat 166800

aatctcactg cagaaatcgt gtttgtatca cagctctgcg gccacccacc ag

#tggtgagg 166860

ccacaacaaa ttatttaacc cctttatgct tcagtttcct cagacatgga at

#attaataa 166920

tagcatgaac atattttatg gtattggtgt gaaaagtaat ttaaatgatg ta

#tttaaata 166980

gctgggcata gtgtctgacc ttagtaacca atcactatta catatgtcat at

#tttcaata 167040

tatctcgtgt taggaactta gtagatatta gatttaatac atactaatta at

#tggtaaat 167100

caatcgtttt atacatttaa atttaaaaag cagttcatgt tcaaattttt ca

#taaacctt 167160

tgcatatttc tcaccaccca tccaagttga acttgaaact cgtaatgtaa tg

#cctgctaa 167220

atcattgtga gagccataaa ggaaaagcct cagcatctga actacaattg at

#cagaaggt 167280

gttagttttc tgcaagaaat gtgtccggtt ttttcttagt agctccattt gt

#tttacttc 167340

ctctggcagg aatgcaaatc attgcatgga gagtatgttg gacgggcctg tg

#gccatgat 167400

cacccatatg ttccagatgt tctattttgg tctgtgatcc tgttcttttc ca

#cagttact 167460

ctgtcagcca ccctgaagca gttcaagact agcagatatt ttccaaccaa gg

#tacttaga 167520

ctatttcttg atctaaatgt aaaataacat aggacaaaag aaagagtaat tg

#atgtaata 167580

aaaggagcca ctgaaaggct tttgtgtgag tgagctgcca ggttagttgt gg

#agtgagat 167640

gaggggctga agagaaagaa tttgtgatgc aggtgctggg agtgcatatg ca

#ggcttttc 167700

tcctaactgc aaaccccacg gatcaactcc tactttccta ctgacgtttt tg

#gaaattca 167760

cagcacacac tgcattactg attgtcactt ttttgcccag tgaacagtgg ga

#actattcc 167820

agcctgacag atacctcaga ggagcctatg ttacattctc taattgggga ag

#ccccggca 167880

agactcattg gaacaatatt ctctttttca atgtttaaac cgtcagtccc tc

#cccctaac 167940

ccaccacgtt tgcatctgca tatttggaaa ggaaagtaaa cagagaaaca gc

#ttagttca 168000

atatttaaca ctgcaaagta acacctataa tgtctgattc cgccaaaaaa aa

#tttaaaaa 168060

aaggaaaaga aacaaggaaa caagcttctg agggatgagc tatagattat ga

#tcaaaatt 168120

ccactctgga aaaatatttc aagaactgtt ccttccgaag ggggcttctt tt

#ttgtcacc 168180

actttcttct actaaaggtg gaagattcat ttatttcccc aaaaatctta gt

#ctgattaa 168240

tacaaaaaca tttttctaag ctgaaacaat aatcttaagc attttgtgta tg

#cttgtgtg 168300

tatgtcataa aggcatctta aaataaacta gatctggata ataattatat gt

#gaatattt 168360

gctcagaatt ggctttataa atgagaaatg gctttaaaaa ttggctcaca ta

#gaataaat 168420

tttaaatttg cccactctgt tgtgtacatt cccaactgtc atgcttatat tc

#tagataaa 168480

ctaaaacatt atgtttcttt gataagaaca gataatttta ttttatgatg ct

#tcaagttt 168540

atcatattaa agtgttacct gtgtgaaaga gatccctaaa atccagccaa at

#tctgccca 168600

tgctacctta ttctgcattc tgaatattca catgcatggg ttcatcataa ag

#ttagattt 168660

taaataaaca ttgaaaacag cacaaccacg atgtagctat tccataatgc ct

#cattctgg 168720

aaaggttgag tgtgtaccaa tcttaacgac agtgatacat aaatatatat tc

#aggttctg 168780

acagagctaa tggtaatctt atagtatgca taaaatataa tattatgata tt

#atgtcata 168840

aagtgtttat aaagtgtgac tctagattat gttcctgagt attccttgat at

#ttatagct 168900

actttaagtg acaagtgttt tcattatttt taggttcgat ccatagtgag tg

#actttgct 168960

gtctttctta caattctgtg tatggtttta attgactatg ccattgggat cc

#catctcca 169020

aaactacaag taccaagtgt tttcaaggta cttactatct ctctccctct tc

#ccatctct 169080

ctcggtctaa tcttcattta gatgatacct ataactctag tacttaggat tt

#tcatgaaa 169140

atatgaagaa tttagattag aagaccagta aatgaaatgc acacagcatg gc

#taaaattt 169200

aggtctaata tttaaaaata taagaattac aaaatataaa taattataaa ta

#taaaactt 169260

gcttgaaaaa aatttcctgt caattctgcc agttgaaata cctatatata ac

#attcttaa 169320

aagataagga agcatttgaa actaagagaa aaggattatc ttggcagaat tg

#tacagtga 169380

ataaggcttg gaaaacagat aaaaatagat tgggaataga attctgaccg tg

#ttactaat 169440

ggggtacagt ttgaatattc cttatccaaa gtgcttggga tcggaagtgt tt

#cagagttc 169500

attttttttt caaattttga aatatttgca aacacataat gagatatgtt tg

#gggtgggg 169560

cccaagtcta aatacaaaat ttatgtttca tatatacctt atacatataa cc

#tgaaggta 169620

attttataca ctattcttaa taatatatgt gacctatcac atgatgtgag gt

#gtgaattt 169680

tccgcttgtg gcatcatgtg agcgctcaaa agtttcagat tttggatcat tt

#cagatttc 169740

agcttttcaa attaggggca cccctttgtt ttctctgtca aacagggctg gg

#gacttcta 169800

tatagggctc ttgtcaggat gaaattttga gaatcatctc agacagcagc ca

#tgtttgga 169860

atccttccct gagcctctgc tgtgaccaag tatctttttt atcattttca ct

#caatagcc 169920

tctgcacatc aaaaataaca gttacaatac cataatgatg tattttgttt ag

#atgtctgt 169980

ctctgattct aaactgaaag aagcctctga tttatctttg tatctcagtt ct

#agcacagt 170040

ggtcaatgtg tcaatatgct atttgtaaat ttcaatacat tttccaatag ta

#aatagtaa 170100

atattaatat cattttattt aatacaggta ttgattaata acacagattt tt

#caacaagt 170160

ctgtcagagt ttaaatccca tctctaccac gtactagctt tgggatcttg gg

#caagttac 170220

tggatctctc tgtgcctcaa ttttcttatc tgtgtcatct ttagagtgtt gt

#gaagaaaa 170280

aaaaaatgag ttaaaatatt taaagcactt aaaatggttt taagtgattt at

#gagtatta 170340

ttattattta ttataggcca ctcagctcct ctgtttataa ttagggcttt cc

#tagtagca 170400

tctgtaagac ctaatttgat caagtattca ttaatccagt tcataactat gc

#acattctt 170460

tactttatac agcccactag agatgatcgt ggctggtttg ttacgccttt ag

#gtccaaac 170520

ccatggtgga cagtaatagc tgctataatt ccagctctgc tttgtactat tc

#taattttt 170580

atggaccaac agattacagc tgtcatcatc aacaggaaag agcataagct aa

#aggtatat 170640

tttaacatcc attttaatgt aaataattat gacaactgat atcaactgat gt

#tcatttga 170700

cttctatatt ctgtattcat ttgcacagtg aaatatataa aataatgttt tt

#agatgtat 170760

aatttttatt gtcttacaag atacttggtc ttacaatgag atgagaattt ac

#ttatttgt 170820

agcacttggc tgagctcacg tctgagaact cacctccaag gcataaaata aa

#aaactgtc 170880

aaagttttaa cttttccata cttaacatat tttaatgaaa taacaatctg tt

#ctggtgaa 170940

gtacaaccat accaacttgt cttacatctg agattcctct attcctctat tt

#aaccctaa 171000

atgtatctat tacattgaat tcattatcag aataaattac aacttcaact at

#ttctcatt 171060

ttctttaatt atttttctgt ctgcctgtaa caacaaaatc cagacataaa cg

#tcacagtt 171120

tagaagtgac atctttgagt tttattgcag atttcactgt ctcttttata aa

#aagaataa 171180

ctatagatgt gtcttagtta cattctgacc ttgccatttt gcaattgtga at

#aatcgaaa 171240

ttgttcactg gtatgcaatt tgcctgagat atgtaatgta agcactgtca ct

#tacttaca 171300

ggaatatgtt aaataaaatc gatgaaatca ttaaatggtt aaaaataatc tg

#catcaaac 171360

cttgtaaaaa cataacatgc acaatcttgt ttttgttttg gtatcgtggg gt

#agttgcca 171420

gctattttca catacccttt aaactctagg agaaaaaatc attgtcagag ca

#acagaaat 171480

catgctttat agaatttttt tataggaatg ttagaaagat gaaaaatatc tc

#tgattaaa 171540

ctctgatgca atatattggg tcaatgcaaa agtaattgca gtttttgcca tt

#acttttaa 171600

taataataat tacataaatg taagaaagca cacttatttg caataaatct ta

#tgaagaag 171660

gaattttgag tatatggtgg agagaatgtg tgtctatctt aaagcaaagg ac

#atttttca 171720

ttctctttgt agaacgtaag ttaagaattc tcacaacttt atgtatttta tt

#aaatgata 171780

cattttaaaa aatcaactaa aaaacctgtt ttaggaagaa agtaagccat at

#aattatta 171840

tttacctttc aaaaagattt ttttagcctt tataattagg cagaaattct ag

#tgtgttca 171900

ctgaaaaatt atcctctgta agggccatca gttaaatgga ttcaggcagc at

#ttttttct 171960

tattgtaagt ggaatcatat taaaacaaag tgtggaagtg aaatgtgtgc tg

#agattgat 172020

attaccttcc tggccattct gaatctttgc cctttcaacc ttataaatca ca

#tgacactt 172080

gctcttactc cttgttcttc atgagccctt gacattcaca gcctttgtaa ag

#ctccacat 172140

tgacaaatac actaatttcc cccttcacat atactgtgga ataacaaaaa tg

#tagtaaag 172200

cattctttaa gtggtccttt caagtacttg catttataga attaaatgca ga

#actagaac 172260

tatttttgtc actgaaataa acctgaggct acattactaa atctgtttta tt

#gtgcaaat 172320

aaatgattat gtagtcaaaa gttgtgtatt tttgcccctt actactctgg at

#ttagtaaa 172380

tgatacagca aatctggctt aatcataaac tctgctatat ggccacaggc ag

#aagagtca 172440

gcctgttctt ggccactgtg aatctgaact ctccatcctc cttcttagat at

#gaatactt 172500

ttaaagcaaa tttcttccag tgaagatgta tttcatctac attgaacccc ta

#ttgggcct 172560

ataactcttg tctcctataa gcttctatag agtgtggtct gatgctactg gt

#tttcccgt 172620

taacaacaac aaaatcacct tctcagaatg ttatttactc agagtaacgg tt

#tgttccat 172680

agtccttctc cccgcctgtt gcttcattga aatgtttgca aagtctcctg gc

#tttgactt 172740

gaaccacatt ttcactaaaa gatgtgtttc ttgagtatat caccagacca ca

#agctaacc 172800

acttgtgaaa gcattttcag cttttactaa ttttcttttc tcacttgaaa ac

#ccattttt 172860

gccttggttg gagcattccc cgaaattgtt taatgaatca tgttttgtag tt

#tatgtatc 172920

aaacacttgg tagactccac atcatgtatc taagtctaca tacacccaag tc

#aactcaga 172980

attcctcatt tcattcttta tctctcccaa acatatttta gatcttttta ct

#ttttcttc 173040

acctctattg ccagaactag tagctggttt tcttttagat gatatttctc ct

#gctgataa 173100

aaatgttttt attggccagg cacagtggct cacgcctgta atcccagcac tt

#tgggaggc 173160

cgagacaggt ggatcacgag gtcaggagtt agagaccagc ctggccaaca tg

#gtgaaacc 173220

ccatctctac taaaaacaca aagattagct gggcgtagtg gcgggcacct gt

#aatcccag 173280

ctactcagga ggctgaggca ggagaatcgt ctgaacctgg aaggcagagg tt

#gcagtgag 173340

atgagatcat gccattgcac cctggcctgg gcgacagggt gagactccgt ct

#caaaaaaa 173400

aaaaatgttt ttatcatttc atgagtgtca ctatgtacac aataaagctg tg

#ttgcactg 173460

cataggtgac ttactactcc cgaagaatgg gggagctcaa aatcagtaaa cc

#tcgaactc 173520

attgcatcct atgatccttt ggatggctcc agagtgaaag aagaggcaaa ta

#caaaaatt 173580

tgagaatgtg aagtatcatg tatattatac ataaatgtac atataaatcc at

#actctctc 173640

tagcatttgt ttgtttgttt ctcccttaga gaagtggatt aggcataagt ta

#actgaatc 173700

cttttgaaaa gcattaaaaa tatctacttg ggttttttaa agcacattct ct

#aaatgtga 173760

aaagagagat aaaatcttat aaaaaagaaa gtttctgtta agatacaact gt

#gggctttt 173820

ctacatgttt ctgtagacag ttcaggcttc ttttgacatc atttttaata aa

#cagcaata 173880

caatcccgga tcacttgagt aaatgaatgc atttgcaaca ttcatttggc ac

#catattct 173940

cttgatgatt atggcatttg atatgttctt ttttgccctc tttgtcagcc tg

#gttcttca 174000

tgtcaatcta tagtctttta tgtggttaac ttgacagatg caggaaattg ct

#gccaagct 174060

ttgaaatgaa ttttttcagc agtggcatct gggtatcaga tggtcctctt gg

#ctggcctc 174120

ttgtcttgct gcatgttggt tttagtgggg tctggtgtag catcacctgt tg

#ctatgctc 174180

ccttttcctc ccatatgtcc atttcctgtg attcatggat gaatgtgaga at

#aaaagctc 174240

tagctctgtc tttatttgag aaaaaaatct acagaaatat gttagaaggt gt

#agagttct 174300

ctgtctgaca aagggatact tctctttggc tggcatgcct atcagctaat aa

#ttttgtta 174360

caaagtccaa gtttttaaag acattttaaa tgaaaggcaa gaaggatact gg

#ttagttag 174420

gggaagagca agaactgctt tatttatttc ctttggttta cgttaaatca ag

#atgctgcc 174480

attgttgtac agcataatta ggggaaatta tatttttgtt tttgttatat at

#ttatatat 174540

tacaaaacta gctttataaa tttagaaaag aaattatttc ctctgaaaga at

#tattttgc 174600

ctacttcctg caattcagaa tcccactgtt tacatttgta tcatattttt aa

#aacattca 174660

ataagagcta ttggaaatca ctatcgcgac aaagatctcc ctcatattat tg

#agatgtag 174720

tgaatgtgga ctctgagaaa gtccaggtgt gctaaaaagt acaagcctga ct

#ctcaaggc 174780

cccctgtctt ctgccctcct ctgatgctca tctcacagcc accagctcct ct

#tccatctt 174840

ttgatttctc ttagcagtac cataattttg caaaatagct ccaagggggc ac

#cattcaca 174900

ttgtactccc tcagaggcag aggcttaagt atgaggtcct tccctgttct ac

#atccttct 174960

cactccagag ttgctaggac aaaacacttc tcaaactgct taagacattg tc

#ctttaaag 175020

ggaccaaaat ctgagttcta ttctatggaa ttacatcttc caaaatgttt tg

#caaaaggg 175080

ccaagggatg atattatggt cctggcaaaa ctgtttccta tgcttttttg gt

#tatgctga 175140

caccaggcag tttctcttcc tactcttcaa ctcttactaa tcaaattctt tc

#ttgagtta 175200

cttgcaaaga aaagtttcca gagtcatatt cattcaggaa attgagttag at

#attttggt 175260

aaattgtagt attgccccag taagctgaat caatgaaggg taccattgct tt

#ggtgtcaa 175320

cataggagga acaggtcctt aggcacataa ctctcattgt ctcctcacta tc

#atctcttg 175380

cacttttata atttggaaag gatgagcaga aaggaaagaa agtacaactg ac

#tttaagaa 175440

ccttcttact aagaaaacaa gaaaacaaaa tcacagagaa aagactacca tg

#acaaatat 175500

gcaacaaata ctcagtgtgt ttcacactcc aggctataag agctctcata ct

#gactacaa 175560

actgcttgaa gttatataaa actacctcta aaaaagacta ttattctcct ag

#aagaattg 175620

gtaatttctg ctcatggtca taataacaaa tttaactgct gtatttattt ta

#aaattaca 175680

cttactaaat ttgattctga aatgtttgat gcgtatttta ttttcaaaaa ag

#tcaatttg 175740

taacttttat tgattgctta ttgtgtgcca atgattgtgc taaaaactag ag

#gaaatact 175800

gagaaattat ataagttatc tgatcttaag aaacatatta atagttttat ta

#aggagcct 175860

tgaaacctaa tgagtacaaa agaaacattt attgtttaac cactagaata ta

#atagtacc 175920

taacatttta ctgattgctt tctattcaac agatattatt ccaaatgatt ta

#caacatca 175980

actaatttaa ttatcacaac agcccagtga ggtgccttct actatcatca tc

#atcgtttt 176040

tcagataggg aaaaagaggc acaagagctt aagtgattta ttggttgagc ta

#gcatttca 176100

ttccaggcag tctgactcca gaacttatat tcttaaccac tttattatac tg

#cctctcat 176160

aaagcagtca ctaaaaatta aaaataaaag gtggaacata aaataggcca tc

#cctttggc 176220

tgcttctgag gctctacact tcgattcctg cagggtatgg agggagtgct ct

#tccccatc 176280

tttgatttcc ctcctcagag agcaccctgt ctgcaagagg gcagttttca ca

#caccccat 176340

tgcacctatt tttcctcctt tacatttcct acctggtcct aggaggcact ta

#gtttgcaa 176400

cacctggaga tcagtgacag tggagtagca taacagagga aatagaaaac aa

#aaaaccgt 176460

gatttctaag gaggggctta atttgtctag tgctgaaact gaagcaaatt ag

#aacaagat 176520

agcactatat taaggagaaa atgactatac aggggagctt aggctccatg at

#attatttt 176580

ttctaataga agtcacccaa tgagacaaac gagggcaatt ggaaactgag tg

#tttgttta 176640

agagttactc caggagatct gatatgaagg gcttgttgag tatcatcagg aa

#gtggtttc 176700

tattcgcaat caggccaccc ttagccctgt tattgacaca gtttctttct ct

#ctttcttt 176760

cttttttaaa cagaaaggtt gtgggtacca tctggaccta ttaatggtgg ct

#gtcatgct 176820

cggtgtatgc tccatcatgg gcctgccatg gtttgtggct gccacagtcc tc

#tccatcac 176880

tcatgtcaat agcctaaaac tggaatcaga atgctcagct ccaggagaac aa

#cccaaatt 176940

tctcggcatt cgggagcaaa gggttactgg gcttatgatt tttattctta tg

#ggttcatc 177000

agtctttatg accagtattc tgaaggtaac aaaatctgtc tttatgaact tg

#agagaaag 177060

aatacattta tcatcattta agattttcat ttgaatctga gccataaatt tg

#caaatatt 177120

gtgtggcatg tgatgaaagt gatgaatttc tgaaccatgt ttatataatt ct

#tcataacc 177180

taagggaggg aaattacgtc ctatatttta aaacccttaa atacataaaa at

#ttagtctg 177240

gcaaagtaaa atttgatgag taaattattg taacaatttt gaatcggtga tc

#aagctatg 177300

ggaaaaagtc actcattgtt tctgactgac ttgtgacccg aatccattac ag

#gcattcat 177360

aaagattcta ttttcttgtc agtggataaa tatattagca gttaatatta ct

#tactatta 177420

ataagagata gaggtgaagg gatgagcctg gttatagtca catacgcagt tt

#tccatttt 177480

aagtgctctg taaaaccact gtctggacat catcattgca tatagtgatt tt

#tttttcac 177540

acaaaacttg aaatctattt ttaagaggat taactagtaa ttattttgtc at

#gtaatttt 177600

gtcagatatt tccaaggtgt gtcaattgcg ctataaatta caacacattt ta

#tttgccta 177660

taatttgaca ttttaattaa attatttaat gatttacact agtttacttg ta

#tttgatca 177720

ttaacacaag tacctttgca agaattaatc tctgttatat aagtaattat gt

#tatagaca 177780

taagatgatg tgaactattc caataaaaag agaaaatctg aattatccat at

#atttacaa 177840

atacctggta taatacagga aacacatcta aatgttagct tcatttttaa tc

#caccttta 177900

atccaaatat cttatctttg taaagcaaaa ttcaagttgt ctccaaagta gc

#ataataat 177960

aatattattg ttcattatat actacatggt ttttaaaaat agattttgac ct

#attaaata 178020

attataacaa ccctattgtt atcatctcct tttagatatt gggaaactaa gg

#cacagaga 178080

gcttaagtaa cttacctaag gttacacagc taaaaatgct agagctggaa ct

#tgaatcct 178140

tgtcttctga atctgtacta tactgtttct attcaaaaat gccttttttc cc

#tgtttttt 178200

tctttgataa atgcaaaacc acaatctatt tgaaaatgat ttctgccttt tc

#tccaattg 178260

ttcttttaca gtttattccc atgccagtgc tatatggagt gtttctttat at

#gggtgctt 178320

catctctaaa gggaattcag gtaaattact tacagtacta caggcacatc tg

#tgatgact 178380

gaccttaagg tctactgata agtcatgtga cagctgagaa aatgccacca cc

#tgaggaac 178440

agcttttaga ccacaattaa atttcttcaa acttgtcaga gttacaaaag tt

#aaagaaga 178500

ttctctccag catctaaggt tcataatctt atggtaattt tctttatcat aa

#gtatatta 178560

aaactgtaag aggcttagat tttacagcat ttttagaaaa atcatagtag ta

#tatttcaa 178620

tatatatcca aatatttata atatttgaca ctttaatcat gtgtatggac at

#ctattggt 178680

aagaatagga aaagtcttta tgcacgaaga tgttcattgt aacacatact at

#taaaatat 178740

tggaaacaac ccaattctct aactgcagtc aaataattag gtaacctatg gt

#atattcac 178800

tgaaaattga taattatagg aaccacaaaa gtaacatggc aaaaatgctt ac

#aacataat 178860

acaaagtaag aaactattga ccataggttt ataaagctat gagtttgagc tg

#ggttgtga 178920

aggaaggtgt agaaataaga acaatttgtt gagatagtga tatcccgggg gt

#tttccccc 178980

ttgttttgtt tgttttactg ttatatttat aggattattt ttaaaattag ac

#taaaataa 179040

agatataagc agtttcaagt ataaggggaa ctttatgaat tatttaagta ag

#tattggtt 179100

aaataaatat tttaggcatg aatttggcaa cagatcagcc agatggttct gg

#ttcaggat 179160

gtcccatgtg gtcactgtca gggtgtggac aaggtccaca gcatctgaag gt

#ttgatagt 179220

gctggaggat ctgcttgcaa aatggctatt ccacaactgt gggcatgagg gc

#atcagttc 179280

ttttctacct gttggtagga tgactcagtc ttttgccaca gtggcctctc ca

#tggaatcc 179340

ttagtgtgtc ctcaaaccat ggaatgtgac tccttcagag tgagcaatat aa

#aagagaga 179400

gagagagata gaggagaaag gagagaagag aatgagaaag aagatgaagt gc

#tttttgac 179460

ttagtcttca aagtcataca tggtctttcc atgttttcta tttgttagag gc

#tatccact 179520

actaagtcca gcttgcaccc aagtgaaggg aaaagggaga ctatctcttg aa

#gagaagag 179580

tatcaaagaa tttgtagaca cattttaaaa cctccacaag tgtattctaa at

#ttttacag 179640

aagctgtagg caaattcttc ccacgtattt ctttgatgat actgttattg gt

#tgaatagt 179700

gagtgtttcc tgaaaattta tgtccacctg gagtctcaaa atgtgacctt ac

#ttgggaaa 179760

tagactattt gcctatgtaa ttagatatgg gtttcaagac aagataatca tn

#nnnnnnnn 179820

nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nttgagtgtg gt

#gtggctca 179880

tgcctgtaat cccagcactt tgggaagccg agtgggcgga tcatgaggtc aa

#gagatcga 179940

gaacatcctg gccagcatgg tgaaacccca tctctactaa aaatataaaa at

#tagctggg 180000

catggtggtg ggcgcctgta gtcctagcca cttgggaggc tgaggcagga ga

#attgcttg 180060

aacctgggag gcggaggttg cagtgagtgg aaattgcacc actgcactcc ag

#cctgggag 180120

gcagaaagag actctgtctc aaaaaaaaaa aaaaaaaaaa aaagaagagg gg

#agaacaca 180180

gagagacaca ggacagggaa gaaggctata tgaagatgta ggaaggccag gc

#acggtcag 180240

ctcacacttc taatgccaga ccaaggcggg tggatcacct gaggtcagga gt

#tcgagacc 180300

agcctgacca atatggcaaa atctagtctc tactaaaaat acaaaaatca ga

#cgggtgtg 180360

gtggtgcatg cctgtaatcc cagctactca ggaggttgag atagaagaat ta

#cttgaacc 180420

cgggaggtga agatcgcatt gagccgagat catgctactg cactccagcc tg

#gacgacag 180480

agggatactc tgtctcaaaa aaaaagaaaa aaaaaaaagg gagaaagaga tt

#agagtttt 180540

gttgccataa atcaagggtg ctaggagcca cctggagctg gaaggggcaa gg

#aagttttc 180600

tcccctaaga ccttcaaagg gagtgtggcc ctggcaatat cttgctttag gc

#ttctggcc 180660

tccacaagtg tggaagaata tatttctatt gatttaaacc accaagttgt gg

#taatttgt 180720

taggacagtc ctagcaaact aatagatttc tacttaaatt gtcccttgaa aa

#gtcttgtt 180780

ttataattta acattattta gcccaacact ccaatgttct tgaaaaagag ac

#tagagact 180840

tattcatcat atagtatttt gtcaactgaa aagcaaaaat aaattgcagc tt

#tttctata 180900

acacagctag actcactgat gttcatagca tataagagaa tagttaacct gc

#aggacagg 180960

cagcacggga tctctgttcc tgagcaaatg actaaccagc ttctgacttt gg

#gagaaaaa 181020

gcagaactta ggccttaaga caatactggc tgccagtctg ggggaaactt aa

#gtatgaag 181080

tcattgcagg tcacggaaca cccaaagttg atagtatgac tgactcttca tc

#ctgacact 181140

gggaaaaatg aactgggaga gggagatggt tgagccatgt tatatgtttt aa

#ttttactc 181200

aaattagatt taatttgctc atttaaaatt tcatgtatga aaagtgtagt tt

#gatagaat 181260

ttgtttagta agccattagg gaagaatatg gaagaggttt tgtttatttg tt

#tttctttt 181320

tccctttttt ttttttttgc ctttggcaaa agttccatga gtactaattt ca

#tctgtaag 181380

tgaaaagcat ttattattag gccccaggct cacataaata cagcagcaga gt

#ttaagaaa 181440

caatgtaaaa tcattttgat gataggtttc aacagatttt ctcctctaat tc

#cacatgat 181500

tttatactca tgagatttag aattgaacaa gaacgtcaag ttttggaatt at

#ttggggtg 181560

tgaatctttt aaatgaaaat tgaagaaaac gttatcaaaa gcccatgagt ta

#aatataat 181620

gagttttaaa gaacacaaat gaaacatcaa tctggggcac atgttgatga ac

#agggtctc 181680

acactgagaa acagtgttcg tgaaaattta agtgagcccc aagagcaggg ag

#ctgaaatt 181740

cctatttgga attgtagcta actgggtggg gaaatgtgat attgatacta gg

#atataata 181800

aaaaccaaat gtaaaactca gaatacattt atcatgatga tgattattat tt

#aaacatat 181860

gctaaatata atcagttcca gcagcatgtt actgtcttac cctattgaag ga

#atctatgt 181920

tacctgcttg tttggcaata ttaagaaact tattatctgg gcttctcact gt

#gaaacatg 181980

gcagaaaaaa cagatcacag tgttctcatg aatgctgttt ctgcattcag at

#atataccc 182040

acatctatat tcattccaac acttcaggaa tccaaagtaa agcaaatgtg cc

#atttaaac 182100

aataacaatt gaagcaccca cacactgaag tacacttatg caataacata gc

#ttcacaaa 182160

tggagaaatg gtggctggga aaaactagtt ctatagaaaa ggaaatattc ca

#ttgtaagc 182220

cagaagattt tattttattt ctttcctatt cctacctcta ccatgcacca ag

#tttttgtt 182280

tatttaatga cttttaagtt taaataatat ttaggaaata gaaattttaa aa

#cttaatga 182340

catgtacatg gacagaatgg agagacatta ttcaggaatg agttcagcac tt

#agtagcct 182400

gcatagaatg tttcaataat atttttggaa tatataaatg aatatgaata aa

#tgaatggt 182460

cagggaatga actaatatat gtatgattct tatttagata actgaggaaa gg

#aaggccat 182520

gtcatgccat aagacataga acacagaagg gaagataggt ttatgttgag tt

#tgagattc 182580

ctattatgta tacaagcagg tcttggtaaa acagggtgtt ttgactctaa ca

#ttttgact 182640

caatggacaa ctgttccttt gcatattaat atgacacatt tgatgagaat tg

#cctacagt 182700

ttttaaaata agttagttaa gaaataaaat ctaatattac tttttgaaaa tg

#cataatgg 182760

atgttactgt agagatggca tgaaataaaa cagtgactga cagtgattga aa

#ccattatt 182820

ttctaaataa tcgcctctag ttggaaacac tgaaaattgc aaaaattggc cg

#aagaacaa 182880

taaaccaaat aatctatata aaataaaact atcatgcagt atgatttgtt ag

#taaataaa 182940

atgtgattaa agatttaagc ttcctgtgtg catttaattt ataaaattca aa

#aaaagaaa 183000

aattggtttg cttgattaaa aaagccctca aagtcaaagc tgtaacataa ta

#gtatgaag 183060

tactataaca atagtgttat gtaatactat gtactatctt tatggcaaga tt

#gaaacaaa 183120

taacattgat tgagatgaaa ataattttaa taaaatacaa ctgaaaatat at

#aaatgacg 183180

tgacagtgct gtatataaag ttaatcaaga aattaaatag agttaacaaa at

#ttgctctg 183240

gaacatactt tattaacaaa atttatttag gttaaatttt tatggttaag at

#gtttgtgt 183300

ccataaagac agcatctaaa cttttgttgg ggattaaagg gacaaagtca aa

#acagcaga 183360

gtcaaaataa ggaggttaaa ataccgtact tagcagctgg ataagggtct ag

#aactcagg 183420

agagagctaa ggcagagacg taggtccgtg aatcattagc aagtctgtga aa

#gtcaaagc 183480

catgggtatg gatgaactat tccaggagaa aagaaaacag agaatgagag tc

#caggaatc 183540

ccaatgttga ggggcaaata aaggaagaga ttgtgttgtg acaatgaaaa ag

#aagatggt 183600

taattatgtt ttgcttcaca gggctccact cttcaaggta gcaatattta ac

#attggctt 183660

tctattttta aactcttcta aattgtaacc cgtctccata ttcaagaaaa tg

#tgggctat 183720

tgtttaactg aaattgtagt gtttcagagg gtaagcataa caatcccatt gt

#cttgatgc 183780

cgagatatca acttagtgtt atccaggtat gtcatttaac ccaaaattgt gg

#accatatt 183840

aaacatcaac ttgtcctact tttattgttg tcttacacct aaaaacaatt ta

#gtctgttt 183900

aatcttttag ttctttgata ggataaagct cttctggatg ccggcaaaac at

#caaccaga 183960

ttttatatac ctaaggcacg taccgcttcg aaaagtgcat ctcttcacaa tt

#attcagat 184020

gagttgcctt ggccttttgt ggataataaa agtttcaaga gctgctattg tc

#tttcccat 184080

gatggtatga aacttctgtc aactattttt ctctttctct gatttgctgg tc

#tctttgga 184140

aacataaaca catgaattga aactggaaca acagagtcat tttgaacaat ta

#ttggaaaa 184200

tataagtttt ggcactgaaa gtgtgactaa gatagggttt aagaatgcct at

#gaatttca 184260

gtgattccta ttagttttgt ctctatcact ctgaatgttt gtggtagtct ga

#attaattg 184320

aagctggatg gaaaaatgca ttcttccaaa atttaacatt aaagatacta gc

#aaatatga 184380

aaaattagga tttttaaaat aacattgtat taaatgtttc aggcaagttt ca

#aatacttc 184440

aaaaactata gtgaatttga atgactaaat aatttcataa ttattagtat ag

#ataagaat 184500

gttctcgtgt tcatttaata tagtataaac tattaactac atgtatttaa gg

#aaacatag 184560

tcaaatacat tttataggtt ttttaaaata gcttatttaa tagactccca ta

#ttggttaa 184620

aatcatagtc attattgtgg tgatgtagta agaaaagaaa atgaaggaag ca

#gaagacta 184680

gacaatgttt tatacatata tatctttaat ttttacttta atctcaggcc ta

#atagaaat 184740

tgtttctacc aaaaaccata caggcaaatc tacacctctc attttaattt tt

#tttccact 184800

ttaaactagt ttattattta cttcaggtgt tagccctggt atttgtaaga aa

#gttgatgg 184860

acttgttgtt cacgaagcgg gaactcagct ggttggatga tttgatgccc ga

#gagtaaga 184920

aaaagaaact ggaagatgct gaaaaagaag taagagcaaa atcaatgttt ta

#taaagaaa 184980

gaaaaaagga acatagtaat atttctttgc aaaactaaat tattgttttt at

#ctttagac 185040

agttttgtct ttagacagtg atcactaaca accacaagta gactagtttg ga

#agtttaat 185100

gtttaaaatc ataaagattt gaacagagag agaatgaaga tcttatagga gg

#aaaccaaa 185160

tcctaatgaa atatggaaat actttgtact aaaataccct ccaaattgta ag

#gctcattt 185220

ttctgattcc tctcctatgg atggcagaaa cttgctaata cttaactatt tc

#caaattat 185280

gatcatgcag tgattgtttt tttgttacat atgtgagaac aaaaagaaga ga

#cattatta 185340

ctgttggtat tttcctaggg aacagagttt taatcaaaat attctaatga at

#aattattt 185400

attcttgaaa taggtgaaat gtttagtagg aaaaatgttg atctgatttg ct

#ttcaaagt 185460

gatttaagat tgagtagatg ttgcagaaac ttctggaatt tatttttaca gg

#ctacttat 185520

ttattttatt ctattttata tggtataaca atgtattata agtttcgtgg ca

#tatttaaa 185580

gtttatatgt aagcctgagt ctattttgaa agcacttaat caacattttt tt

#aagtatat 185640

aaaaactaca aagagtgtaa atgagggaaa aataactagc gtaacattta gc

#aggatgat 185700

tgagcccata caatgtaaaa cacaacaaag ttttcacata aatagaaatg ag

#attgaaat 185760

aaaatatttg atgagaatta tactattttt ctctataagt agtcagtaaa tg

#tattcaac 185820

tttctatttc ctcaaaccat agatatattt cctatttcct ttggggaatt ca

#tttgcaga 185880

tgtttcagag gtcttagtca tttaatgagg tcagatcagg ccataaatca aa

#tgaggttt 185940

tttctttctc agaaatttat accaatatgg ttacataatg tgtaattggt aa

#ttccctta 186000

ctctacatgg tgttctatca ctaacaatgg attcccacag atagagattc at

#catgatga 186060

tgtgtcttaa tcctgtaaga atgtttcaat ttttccaaat attgtagaag gc

#aatactta 186120

gactcatact tctagtaata ttaatgttaa cacaaaaaat gatattatac aa

#ttgttatt 186180

atttattttt ctgtttgata tatttttatt taaatattag tgctttttta aa

#aaataata 186240

ctttgagtca ggcgcagtgg ctcatgcctg taatgctagc agtttgggag gc

#tgaggcgg 186300

gcagatcacg agatcaggag ataagaccat attggctaac atggtgaaac cc

#cgtgtcca 186360

ctaaaaatac aaaaattagc tgggcatggt ggtgcacacc tgtagtctca gc

#tactcagg 186420

aggctgaggc aggaggatca cttgaaccgg gaggtggacg ttgcagtgag cc

#actgcact 186480

ccagcctggt gacagagcga gactccgtct caaaaaaaaa aaaaacaaaa aa

#caaaaaac 186540

tttgactagg atattttgat agtctctatt tctttttagg cctttagtaa ac

#gtttgctt 186600

tcatcctcag atactcttca agaaaatatg gtataatttg gcacaagtta aa

#tttaaata 186660

aaacggacac tagaacacag aaattctaaa atcttaagtt atctatattt ga

#tgtaaata 186720

aaattattga gatcaaacac aacacccaag aaggtttaaa ttaatttaat tt

#tgatgaaa 186780

aagctcttgg ctgtgagctt gcctttcagt ctttttgata atgtcagtac ag

#cagaccct 186840

tgaataatat agcattgtta taatgttgat gagaaaagaa aaaaaaaatt cc

#ctggccag 186900

ggccactgtc tgtagggagt ttgcacattc tcctcatatc tgtgtgggtt tt

#ctctggac 186960

acttcggttt cctcccacat ccccaaaatg tgcccattag gttcattggc gt

#gtctacat 187020

tggctcagtg tgagtgaatg tgggtgtgtg tgtgagtgtg tgctgcaagg ga

#atagcgtc 187080

ttggccagtc ttatttctca tcttgtaccc tgagctgcca agataggctc ca

#gccaccct 187140

cgaccttgaa ctggaataag tgggttggaa aaggaatgaa taaatgaata ca

#aatgactg 187200

taaaataaaa attcatcaag tatacgataa tcacacaaat gtacgacaac aa

#tttggtat 187260

gaaaatgctc agtgaaccca gccatatttg ctattgtttt tgaactgctt gg

#tggtaaga 187320

tgtgctcctt acaattttca ctttgcaaac atttattcct gatttaatcc ac

#ccctacta 187380

tggcctcagt cactctctca ctcaccagaa atttggtaat tcaatatctt ac

#ttgctttt 187440

attaactttt cttacatgtt tgtatagctc acatttattt caatgtttaa ta

#ttaaaaac 187500

attttgggtc tttagttaga agtttggtga tgtttttgtg accagatatt gc

#cataggaa 187560

tttaactctt gtttatatca attagcctat ggtaaaattg gttttattta tt

#cttaatgt 187620

cacagtctcc gagaacctat caataacttt atgtgagcac ttattgtact at

#taattata 187680

ctcaagcagt aacttacata tctaattttg ctttattttt ctgctttttt tt

#gttaactg 187740

tctttactgc ttctggaaaa aaaaaaaacg aacacagccc cagacatata at

#catctctt 187800

tcacagtatt ctccttagat catactcata ccgtgaaaca ttcttgcctt tt

#agaagttc 187860

acaaaatgaa aaatgatatg taatctatta tgtaatgttt aatatttctg tg

#actgtgat 187920

tcaaagataa tttcagattc tccttttatt ttctgtgaaa caggagagaa ca

#agtttaat 187980

aataattgta aatttattag aatttgccat tcccactgcc cagaaccact ca

#catagcta 188040

tgcatgtatg gtacttatat gtgtgtgtgc catatgccca ttttggaatt ta

#tgaatctc 188100

atagggcaga gaacatatgt aatcagtgtc taatcttttt atattatata cc

#cactgtac 188160

tttaatgggc atttactgtt ctctgattat gaagataaag attttaaaag ta

#actaaata 188220

gcactaaatt tcctagaact catgctttct gaaaagatac aaaaatggat ta

#aagatttc 188280

ctggggcaat tttactgcta aatccttcat atccaagtta gagggaaaag cc

#ttgcagta 188340

cattaactag gcaggtttat agatccttaa aatctcagat gggttaatat ga

#tgatactt 188400

tcatgtgatc ctcagtacat ggaaagaaac aagaaaatca ataatatagt ca

#agaaataa 188460

tctataattg aacaataaaa tatagctctg actagtgcaa agacagctaa tt

#ctccatcg 188520

aacaggaaag aaaataggaa gtttaaagag gttcgctttc tagcttagaa tt

#agtattaa 188580

aagagtatgg tcactaaaga cattaggaag atttaggaat aattatacta aa

#agttaaat 188640

tcctggttga tttgtttgcc cggatcttgg tattctattt tcttgaggct ta

#cagactca 188700

gtagaaggat gtgatcttac tgtggcatct tatactaagg cccagtcttc ta

#agagattg 188760

tgtgttaagg tggtaaacgg acaagttctc cagaaatgtt gcatttctgc aa

#ttgctcaa 188820

attaattgag taactttgat catgaactgg caagatggta aatagcagaa at

#gtctcagc 188880

tccctgagac ttgaatttaa agtaggctca cctcttgtcc ttttgatgat ag

#atacaagc 188940

ttttaccttt agcctccagg gttttcctat cagtagccca tttctggtct ta

#tggcactg 189000

agaaaacatt catttgacct taaaattcaa taatgagtta agcagaataa at

#agctacac 189060

aggccagtcc aaggtcgcag agcttctgtt ccaaattttc atgtacttca tg

#catatgca 189120

tatgcatatg cttcagtttt tagaaagaaa ggattataat cagggtagaa at

#gaatattg 189180

gaaccctgac attttgcaca ttgctctgtg taaagggaag actgcagaat ca

#aattctgg 189240

atgtccaaat gtgctcagag taccaacatg ccttccttcc tacttaaata tt

#ctctaggc 189300

cattgtacac atttgacaaa aggctactta ctgttaaagg cagaaaatcc ca

#gcagaatg 189360

tttgctcctg ggtaggagga aagggggtta gtgttggata aatcctagaa at

#tctactct 189420

gtggaagtga tcatgatagt gatacttctt gatttactgg ggcttcactc tt

#aacatata 189480

cactatagga gaaaacaaaa agagggcaaa tgggaccctg tgatcccaat gc

#aggatcat 189540

gaaaaaggtc aagaaaaaag caatctaaaa acaagtgcaa ctaaacaaat ta

#cagaggac 189600

gacttactgc taagataggt cagaattggt tatggatttg ggaagcatgg cc

#aaattatt 189660

acannnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nn

#naacaaag 189720

tatgctagct atgggaagat gagggcacag tacaactccc attggaaggg ca

#ctataggt 189780

aagacataaa tttaaaaaca catcaattaa agtaatgaaa tgcattgtta ta

#tactttaa 189840

gaatttcata ctgtgtagat cctcagagag gtttcttgaa attgtataag ag

#tagaaaga 189900

acgaagagtt agataacatg ggtcctactg ctaagttttg ccaataatag cc

#gtgtgact 189960

ataatcaaat tgcattaaat gaagtgaagc aggaagctgt tgtctgaagt tt

#ttcttgct 190020

cctgttttat aatgtgtatg aaaaatccct ttcatattct cagaaagtag ca

#ccagaaga 190080

cagatcaagg ttcctttttt gtataagtga ctagttattc actaagttga tc

#acaggtaa 190140

atgttttaac tctgggaatt tgccgctaaa agtggaattt ccaatgacat aa

#tctatttc 190200

ttaagtgatt cagttgtatc agtcatttta ggatatattt atgcaattct cc

#aaaatttt 190260

ctaatcttct ttatgtacaa agacatagca aaagaaagca aactactgaa gt

#tataaaga 190320

aaacatttgc aagcatttgg cccagaattc tcccctctct ctctcttctc tg

#tctccctc 190380

tcaatatagt ttagtttaaa cggttatctt gtacaattct aagtatcaat ta

#gtgcccaa 190440

ttttatagtc tcaaagtctt tatgaataat ttaaggttat gccaataaaa at

#acagagaa 190500

tactttttta tgagaaggga atttgtcata gtgttaaaaa ccaaaatagg ag

#agaatttt 190560

ctagatcttt agggtctgac tctaagatta tattccctag aatttaagaa aa

#tgtgatta 190620

cctccctctt aagagggggc acaagtataa gatgttttat cttttttttc tt

#ttttacaa 190680

catttaaatt ttaaaatcct gttgattttt tagctgaacc agcatatttc ca

#agtgtatt 190740

aggtagaaac ctagtcttgt gtgataccac tctcgaaagg gctgtgtggt ta

#aataagtt 190800

tgaaaaaatg tgccaaactg cattccagtt tggagattca caatgcatat ta

#gcaaatga 190860

aacaatctaa gtagtactgc attttaaaaa attgtatagc ttcgttcaat ca

#agtattta 190920

aaaaaatctt ttgctcagaa gactcttcct cacataatat catgaaaaat gt

#ctattcca 190980

catgatgctt tttttaagaa agtagtcaat ctggtgcttt gaattaccag ga

#aactatct 191040

ttctaggaag accaaaacag ctggagggtt tagaggaact gaagaacaca tt

#tccagatt 191100

gggcaagaga gggagaccca aggttttgtt cctcttaaaa gttgcatttg tt

#cctctcct 191160

gtgacctatc accaatcagg gtcatatgaa aaggcggcat ttgaacaaag aa

#ggggcaag 191220

gttgctccat gtgaagggac atgataagca gagggaagag caaggacaag gc

#ccccaggc 191280

agcaccatgc ccattgtgtt ccagaacagt caggaggcta ctgaaatggg gc

#tggaaagg 191340

agtgagcagg gatgcagtgg caggaggtga aatcagagtg aggtggggac ag

#agccttta 191400

ggccattata aggacttggc attgactctg agtgactggg agccactgca ag

#gtctgagc 191460

aaaggaggga agtgatctgg ttgctatgat gttaggggca agcgtttaag ca

#atggacat 191520

gcggaaccca ttctctgtaa tttgaaatga attaagaata ccacaggcca ac

#tcagtatc 191580

tattcaacta gaatattttc tttagttttt ttatttttca cagattgttt tc

#aataattg 191640

agagaaatat tcaatacttc ttcattttta attatcaaaa atattgtaca at

#aaacaaaa 191700

tggggcatac acatacaatg gaacattatc caggtttaaa aaggaggaaa tt

#ctgacata 191760

tgctacaaca tggatgcacc ttgaggatgt tgtactaact gaaataaacc ag

#tcacaaaa 191820

agacaaatac tgtatgattc tgcttatatg aggcacttag agaagtcaga aa

#cctagaga 191880

cagaaagtgg aattatagtt gccagggacc gggaacaaga ggaaatggag ag

#ttgtggtt 191940

tagtgggtat ggagttccag ttttatagga taaaaagagt tctggaaatg ga

#tggtggtg 192000

atggttgcac aacattatga atgtatttag taaccctgaa ctgtactttt aa

#aaatagtt 192060

aaggtagtaa attttatgtt atgtgtattt taccacaatt taaaaattgg ga

#aaaatatt 192120

cttcatagat atatgattgc cctatattta gtttctgtca ttgaaaaact gc

#agttactt 192180

atgtaatgtt tattatttca tttggggaaa ctcctgtcta gagatgatcc at

#ctgtgatc 192240

aatatatctg atgaaatgtc aaagactgcc ttgtggagga accttctgat ta

#ctgccgat 192300

aactcaaaag ataaggagtc aagctttcct tccaaaaggt ttggatttta aa

#ataatgag 192360

aatttatact aattccaatt gttttttgac ataaaccata agcaaaagaa ta

#atattagt 192420

ttccatcaaa tttagatata aaatattcca gaaaattctt tccaaaagtg gg

#tagaaatt 192480