iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

Abtb2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs3708133	snp	A/G	0.5	0	intron-variant	Abtb2	Mm_Celera	2:103574097	agccctagtgaccca[A/G]cctgAGTGAGCCATC	99382
rs6219381	snp	A/G	0.5	0	intron-variant	Abtb2	Mm_Celera	2:103715194	tgggcctcaaacttg[A/G]gcaatcctcccatct	99382
rs6219974	snp	A/G	0.5	0	intron-variant	Abtb2	Mm_Celera	2:103715314	AGTGGGGTGGGAGAG[A/G]GGGTAGNGGCCCTGC	99382
rs6219992	snp	C/T	0.5	0	intron-variant	Abtb2	Mm_Celera	2:103715321	TGGGAGAGNGGGTAG[C/T]GGCCCTGCTTTGGAA	99382
rs6220480	snp	C/G	0.359862	0.224567	intron-variant	Abtb2	Mm_Celera	2:103715389	TCCTGGGCTACAGAG[C/G]TCTCATAGGGAAAGG	99382
rs6220969	snp	A/G	0.5	0	intron-variant	Abtb2	Mm_Celera	2:103715459	GCAGTATAGCTGTGC[A/G]GCACCACACGNGTGG	99382
rs6220987	snp	G/T	0.5	0	intron-variant	Abtb2	Mm_Celera	2:103715470	GTGCNGCACCACACG[G/T]GTGGTGTTTACNTAA	99382
rs6221001	snp	A/G	0.5	0	intron-variant	Abtb2	Mm_Celera	2:103715482	ACGNGTGGTGTTTAC[A/G]TAAGTCCGTTCCCAC	99382
rs6221486	snp	A/G	0.290657	0.246672	intron-variant	Abtb2	Mm_Celera	2:103715577	CATCCTGCAGGTAAG[A/G]GCAGGGCATGTAGCC	99382
rs6310195	snp	A/G	0.5	0	intron-variant	Abtb2	Mm_Celera	2:103693612	TAGGTAAAGTCAGCC[A/G]GACATGGTGACACAC	99382
rs6310622	snp	A/G	0.5	0	intron-variant	Abtb2	Mm_Celera	2:103687078	TTTACAGTGTTTCAG[A/G]TCTCTCTTCTCCCTG	99382
rs27358068	snp	A/G	0.42	0.183303	intron-variant	Abtb2	Mm_Celera	2:103678537	TCTGTCTACATATTG[A/G]TAAAATCCCAGGAGA	99382
rs27358069	snp	C/G	0.21875	0.248039	intron-variant	Abtb2	Mm_Celera	2:103678391	ATCATCCAAACTGAG[C/G]AAGCATAAGTGCTAT	99382
rs27358070	snp	A/G	0.49827	0.0293608	intron-variant	Abtb2	GRCm38.p3	2:103678320	GAGAAGAAATGGACT[A/G]AGTGGGAAGGGGGAA	99382
rs27358071	snp	A/G	0.497041	0.0383476	intron-variant	Abtb2	Mm_Celera	2:103678280	GTATCCCTTTCCAGT[A/G]ATGTCTCCTGGCCTT	99382
rs27358072	snp	A/C	0.18	0.24	intron-variant	Abtb2	Mm_Celera	2:103678269	TAGAGAGGGCAGTAT[A/C]CCTTTCCAGTAATGT	99382
rs27358073	snp	C/T	0.497041	0.0383476	intron-variant	Abtb2	Mm_Celera	2:103678245	GCTGGGACAGTCCCA[C/T]TCATGAAGTAGAGAG	99382
rs27358074	snp	A/G/T	0.277778	0.248452	intron-variant	Abtb2	GRCm38.p3	2:103678026	ATCAGAGAAGTAGCA[A/G/T]CTCCCCAGAATTTGG	99382
rs27358075	snp	C/G	0.35503	0.226867	intron-variant	Abtb2	Mm_Celera	2:103677864	CATCCCTGCATGCCA[C/G]AGAGGAGACTCTTAG	99382
rs27358076	snp	A/G	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103677793	ACATGTCAGCACAGT[A/G]TTTATAAATGCCAGA	99382
rs27358077	snp	A/G	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103677761	CAAGTCACCCACCCA[A/G]GTTCATGTAGCTGAT	99382
rs27358078	snp	C/T	0.473373	0.11227	intron-variant	Abtb2	Mm_Celera	2:103677720	ATTTACGTTCCTCCG[C/T]CATTGTCTCCACTTA	99382
rs27358079	snp	A/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103677459	GCCCCAGGTTAGGGG[A/T]GGACTGCCCCCATGC	99382
rs27358080	snp	C/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103677409	GAACTATCACTGTAC[C/T]TGCAGGGTGATCTAG	99382
rs27358081	snp	C/G	0.415225	0.187619	intron-variant	Abtb2	GRCm38.p3	2:103677262	CCAGTTCTTTCTCCT[C/G]CCATGGAAATAAACA	99382
rs27358082	snp	A/G	0.497041	0.0383476	intron-variant	Abtb2	Mm_Celera	2:103677040	CCCAGTGTTGTTTCT[A/G]TCAATGAAAAAGGAG	99382
rs27358083	snp	C/T	0.35503	0.226867	intron-variant	Abtb2	Mm_Celera	2:103676947	TAGTGACATAATAGT[C/T]CTCACTGGGAATCCT	99382
rs27358084	snp	A/G	0.35503	0.226867	intron-variant	Abtb2	Mm_Celera	2:103676756	AAGAGAGTGAAGAGA[A/G]AGAACAATTTCTAAA	99382
rs27358085	snp	C/T	0.444444	0.157135	intron-variant	Abtb2	Mm_Celera	2:103676724	CTGACTGCATTATTT[C/T]CTTTGTTAGAAGAAG	99382
rs27358086	snp	A/G	0.497041	0.0383476	intron-variant	Abtb2	Mm_Celera	2:103676062	CATTTTCAGTTTCTG[A/G]TGATCTCTGTAAGAA	99382
rs27358087	snp	A/G	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103675984	CAAGATGGCCAAGAT[A/G]AAAATATCATTTCAT	99382
rs27358088	snp	A/G	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103675963	CTTCCAGATACCCTA[A/G]ATGGCCAAGATGGCC	99382
rs27358089	snp	A/G	0.35503	0.226867	intron-variant	Abtb2	GRCm38.p3	2:103675581	TGGTAAAAGCAGTAC[A/G]GCCTGGTGACTGATG	99382
rs27358090	snp	A/G	0.35503	0.226867	intron-variant	Abtb2	Mm_Celera	2:103675579	GGTGGTAAAAGCAGT[A/G]CGGCCTGGTGACTGA	99382
rs27358091	snp	C/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103675546	AGCAGTGGCCGTGAC[C/T]AGTTTTTGAAATACT	99382
rs27358092	snp	C/G	0.497041	0.0383476	intron-variant	Abtb2	Mm_Celera	2:103675524	GAACAGGGAGGCCAG[C/G]GTGAGGAGCAGTGGC	99382
rs27358093	snp	C/T	0.35503	0.226867	intron-variant	Abtb2	GRCm38.p3	2:103675465	AAAGGCAGTTGGATT[C/T]CTTCATACAGACAGC	99382
rs27358094	snp	A/G	0.497041	0.0383476	intron-variant	Abtb2	Mm_Celera	2:103675380	TTTTGCCACTTTACC[A/G]GCAGAAAATCACTTC	99382
rs27358095	snp	C/T	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103675180	GGGTGGAGTTTCCCT[C/T]CTAACTCAACACCAC	99382
rs27358096	snp	C/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103675138	TGGGTGGCACCTCCT[C/T]GTGAGAAGGCAGGTT	99382
rs27358097	snp	C/T	0.35503	0.226867	intron-variant	Abtb2	Mm_Celera	2:103675005	CAGATGAAATCATCT[C/T]CTTTTCCTTTGAACT	99382
rs27358098	snp	C/T	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103674864	GGTTCTGTTTCTTTC[C/T]ACTGCTGACCATTTG	99382
rs27358099	snp	C/G	0.35503	0.226867	intron-variant	Abtb2	Mm_Celera	2:103674801	CGCAAGCACACACAT[C/G]CTCTTATGACTGTGA	99382
rs27358100	snp	A/G	0.456747	0.140554	intron-variant	Abtb2	GRCm38.p3	2:103674616	TAGGTTGGAAGGGAA[A/G]CTATGTTGCAGCCTT	99382
rs27358101	snp	A/G	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103674591	TAGGGAGAATGCTGT[A/G]ATGGGTTATTAGGTT	99382
rs27358102	snp	C/T	0.35503	0.226867	intron-variant	Abtb2	Mm_Celera	2:103674287	ACTCCTTACCCATTC[C/T]TTCCATGGAAAAATC	99382
rs27358103	snp	A/G	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103673914	CTTCCCTTTGCTTCA[A/G]GAGGCACCCATGCCT	99382
rs27358104	snp	C/T	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103673727	CTCCCTGTCTCAGAA[C/T]GTTGTCCTTGTTTGA	99382
rs27358105	snp	C/G	0.35503	0.226867	intron-variant	Abtb2	Mm_Celera	2:103673677	CTCAGTTTGGACACC[C/G]TGCTCCATGTGTATG	99382
rs27358106	snp	A/T	0.35503	0.226867	intron-variant	Abtb2	Mm_Celera	2:103673589	CCCTACTAAGTTTGT[A/T]TGGGCATGGAGTATA	99382
rs27358107	snp	A/G	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103673525	CTGTGTCCCACAGGA[A/G]AATGAGACACTGCAG	99382
rs27358108	snp	C/T	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103673452	TTGCTGCTCAGTTTG[C/T]ATTCCACTTTGCCAT	99382
rs27358109	snp	A/G	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103672873	CAGTTGTAACTGTGC[A/G]TTTTTATTTCATTGC	99382
rs27358110	snp	A/G	0.497041	0.0383476	intron-variant	Abtb2	Mm_Celera	2:103672303	CTTAAAGTATTCAAA[A/G]TAACACAGAGCCTTT	99382
rs27358111	snp	C/T	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103672215	AGAGGTCATTCCAAG[C/T]CTTGTGCTTCTTGGC	99382
rs27358112	snp	A/C	0.46281	0.131194	intron-variant	Abtb2	GRCm38.p3	2:103671111	AGAATTGCTTGGAGA[A/C]ATTAGAAAGGTGAAA	99382
rs27358113	snp	C/G	0.396694	0.202437	intron-variant	Abtb2	GRCm38.p3	2:103671085	GGAAGCTGAGAAAAA[C/G]TCTTCCACCCAGAAT	99382
rs27358114	snp	C/T	0.396694	0.202437	intron-variant	Abtb2	Mm_Celera	2:103671024	ACCAGATCATTTGAT[C/T]CATGTAAATTTGCCA	99382
rs27358115	snp	C/T	0.48	0.0979796	intron-variant	Abtb2	GRCm38.p3	2:103670885	TTGTCTAAAAACACC[C/T]TGAACAATGGGGGGG	99382
rs27358116	snp	A/G	0.165289	0.235211	intron-variant	Abtb2	Mm_Celera	2:103670585	TCAGGATGACTTCCT[A/G]TAAGAGGATGGAAAG	99382
rs27358117	snp	C/T	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103668857	TGAGGGAGCAAGTCA[C/T]TGTGGTCCTGCATGA	99382
rs27358118	snp	A/C	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103668852	CCTCATGAGGGAGCA[A/C]GTCACTGTGGTCCTG	99382
rs27358119	snp	A/G	0.35503	0.226867	intron-variant	Abtb2	Mm_Celera	2:103668810	GGGGCTCCTCTCAGA[A/G]CCCAGGCCTGCTTCC	99382
rs27358120	snp	A/G	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103668650	CTTGCCCTTCCAAGA[A/G]GCCTGCTCCAGGCTC	99382
rs27358121	snp	A/G	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103668243	ACTCCACAAGACATC[A/G]GGTTGCCTCATTCAA	99382
rs27358122	snp	C/T	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103668168	ATCAGTCATGAGTGC[C/T]ACTTGCAGGCAGGTA	99382
rs27358123	snp	C/T	0.375	0.216506	intron-variant	Abtb2	Mm_Celera	2:103667933	CTGCGCTGGAAAGTC[C/T]TCACCCAGCATAGAC	99382
rs27358124	snp	A/G	0.277778	0.248452	intron-variant	Abtb2	Mm_Celera	2:103667922	CTCCAAGGTAGCTGC[A/G]CTGGAAAGTCCTCAC	99382
rs27358125	snp	A/T	0.5	0	intron-variant	Abtb2	Mm_Celera	2:103667348	GAAGGAAAAATAAGA[A/T]GCTGAGAGGAGTAGA	99382
rs27358126	snp	A/G	0.277778	0.248452	intron-variant	Abtb2	Mm_Celera	2:103667273	ATTTTCCCTCTTCCA[A/G]GGTACTCAGTGGGAA	99382
rs27358127	snp	A/C	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103667255	CTGTCTGCAGTCTAG[A/C]CCATTTTCCCTCTTC	99382
rs27358128	snp	G/T	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103667230	ATTTATTTAACCTGC[G/T]GATGGTACTCTGTCT	99382
rs27358129	snp	C/G	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103667141	TTACATACCTGGGAG[C/G]TACACAAAAAGAGAC	99382
rs27358130	snp	C/T	0.497778	0.0332592	intron-variant	Abtb2	GRCm38.p3	2:103667041	TGGAAGTTACATTCA[C/T]AGTGAGCCTCATGCT	99382
rs27358131	snp	C/T	0.277778	0.248452	intron-variant	Abtb2	Mm_Celera	2:103667005	AGAACTGCAGGCAGC[C/T]CAGCATCCAGTGACC	99382
rs27358132	snp	A/G	0.277778	0.248452	intron-variant	Abtb2	Mm_Celera	2:103666861	CAGCACCCGTGCTGT[A/G]ATAAAAGTCACAGTG	99382
rs27358133	snp	A/C	0.456747	0.140554	intron-variant	Abtb2	GRCm38.p3	2:103666816	GCACCTGGAAAGAGA[A/C]GATCACGCTCAAAGT	99382
rs27358134	snp	A/G	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103666814	ATGCACCTGGAAAGA[A/G]AAGATCACGCTCAAA	99382
rs27358135	snp	C/T	0.277778	0.248452	intron-variant	Abtb2	Mm_Celera	2:103666773	GCCACCAGCAAGAGA[C/T]GCAGAACATTACCCA	99382
rs27358136	snp	A/G	0.35503	0.226867	intron-variant	Abtb2	GRCm38.p3	2:103666735	AGTGATTCAGGTAAT[A/G]GAGTCAACCCCGGTA	99382
rs27358137	snp	C/T	0.444444	0.157135	intron-variant	Abtb2	Mm_Celera	2:103666692	AGAGCACTTCAGTCT[C/T]TGTGAGGCTTGAGAT	99382
rs27358138	snp	C/T	0.429688	0.173817	intron-variant	Abtb2	GRCm38.p3	2:103666527	TATTGTTTTTGCTGT[C/T]TTACAGGAGTATTAA	99382
rs27358139	snp	C/G	0.375	0.216506	intron-variant	Abtb2	Mm_Celera	2:103666466	CAGTAAGCACCCTGG[C/G]TAGGATCTGAAACCC	99382
rs27358140	snp	G/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103666391	AAGACACACAGCAAG[G/T]CAGGCATGGAATGGT	99382
rs27358141	snp	G/T	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103666344	TGGGTCAAGGACTGG[G/T]CCCTTACATGGCCAT	99382
rs27358142	snp	C/T	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103664871	GAAGCCTTCTCTTAT[C/T]CTATAATTCCACCTG	99382
rs27358143	snp	A/G	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103664725	GTCCACCTGTGGCTT[A/G]AATTGGAGCTGGGAG	99382
rs27358144	snp	C/T	0.495868	0.0452663	intron-variant	Abtb2	GRCm38.p3	2:103664724	GGTCCACCTGTGGCT[C/T]GAATTGGAGCTGGGA	99382
rs27358145	snp	C/T	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103664715	CAGTGCTCTGGTCCA[C/T]CTGTGGCTTGAATTG	99382
rs27358146	snp	A/G	0.32	0.24	intron-variant	Abtb2	GRCm38.p3	2:103664635	CAAGCCTGTGTGGTC[A/G]CAGAGTTGCTGTAAA	99382
rs27358147	snp	C/T	0.345679	0.230967	intron-variant	Abtb2	Mm_Celera	2:103664634	GCAAGCCTGTGTGGT[C/T]GCAGAGTTGCTGTAA	99382
rs27358148	snp	A/G	0.277778	0.248452	intron-variant	Abtb2	Mm_Celera	2:103664524	GTGTCACACGTGTTT[A/G]TTTGTCAAGCAGGGC	99382
rs27358149	snp	A/T	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103663958	ACAGTCGACAGTATG[A/T]ACTCTCTAGGGAAGC	99382
rs27358150	snp	C/T	0.297521	0.245442	intron-variant	Abtb2	Mm_Celera	2:103663814	TGGAATGCTTACAAA[C/T]TGTGTCATCTCCTGC	99382
rs27358151	snp	A/G	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103663685	CCTTTGAACAGTGAC[A/G]AACACATTTGAATTA	99382
rs27358152	snp	A/G	0.486111	0.0821678	intron-variant	Abtb2	GRCm38.p3	2:103663320	AGGGTAGACCGTATG[A/G]AGAAGCATAATGGGA	99382
rs27358153	snp	A/T	0.18	0.24	intron-variant	Abtb2	Mm_Celera	2:103662934	TAGGTACCATGTAGG[A/T]ATTACATACTCTGCG	99382
rs27358154	snp	A/G	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103662866	TTATAGGAGCCTTCT[A/G]TGTCCACTCCCTGGC	99382
rs27358155	snp	C/T	0.152778	0.230321	intron-variant	Abtb2	GRCm38.p3	2:103662741	CTTTTCAAATGCCAA[C/T]TGTCAAGTCAACTTT	99382
rs27358156	snp	C/T	0.486111	0.0821678	intron-variant	Abtb2	Mm_Celera	2:103662401	CTACCTCTGTCTCTA[C/T]TTCAGCCAGGAGGAG	99382
rs27358157	snp	C/T	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103662316	TCTATGTGATCTCAC[C/T]GGAAGCTCATCTGAG	99382
rs27358158	snp	A/G	0.444444	0.157135	intron-variant	Abtb2	Mm_Celera	2:103662101	AGGAGTCTCTAGATG[A/G]GAAGGTCCTAGGTAA	99382
rs27358159	snp	A/G	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103662046	ACCCTTGCCAGCCTC[A/G]GATGGATGAAATGCA	99382
rs27358160	snp	A/G	0.277778	0.248452	intron-variant	Abtb2	Mm_Celera	2:103661988	AGATTCCCAGCACTG[A/G]AACTGTATCCCTCCT	99382
rs27358161	snp	C/T	0.46281	0.131194	intron-variant	Abtb2	GRCm38.p3	2:103661855	CATTGAGCAATCTCA[C/T]CTGAACATCCCTGAG	99382
rs27358162	snp	C/T	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103661822	GAAAGCATTGCCCTG[C/T]CACGTTGGGAAGGAT	99382
rs27358163	snp	G/T	0.493827	0.0552116	intron-variant	Abtb2	GRCm38.p3	2:103661688	TGAGGAGTCGCAGTC[G/T]TGGTTTAGAGAAGGG	99382
rs27358164	snp	C/G	0.408163	0.193609	intron-variant	Abtb2	Mm_Celera	2:103661683	TGCCATGAGGAGTCG[C/G]AGTCTTGGTTTAGAG	99382
rs27358165	snp	C/T	0.444444	0.157135	intron-variant	Abtb2	Mm_Celera	2:103661644	TTCACAAGGTATTTC[C/T]TGAGCCTCTGTTCAG	99382
rs27358166	snp	A/G	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103661232	TAGATCAAGAAAAGC[A/G]TGGCCAAATGGCAAT	99382
rs27358167	snp	A/G	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103661230	TCTAGATCAAGAAAA[A/G]CATGGCCAAATGGCA	99382
rs27358168	snp	A/G	0.297521	0.245442	intron-variant	Abtb2	Mm_Celera	2:103661113	AGGGCAGCCTCTCTT[A/G]GCCTTGCCAGCCTTA	99382
rs27358169	snp	A/C	0.375	0.216506	intron-variant	Abtb2	Mm_Celera	2:103660490	CCTTTTCAAGCCAGA[A/C]ACAAGCTCTCACAAC	99382
rs27358170	snp	A/G	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103659823	TGATATCCTCACCAC[A/G]TTAGTACTTTAGAGG	99382
rs27358171	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103659728	GTGATGTGGTCTGGC[A/G]AGGAGCCTTCTTCTC	99382
rs27358172	snp	C/T	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103659727	TGTGATGTGGTCTGG[C/T]GAGGAGCCTTCTTCT	99382
rs27358173	snp	A/T	0.277778	0.248452	intron-variant	Abtb2	Mm_Celera	2:103659656	CAATGTCTCACACAA[A/T]GTCCCTTCAGCCTCC	99382
rs27358174	snp	C/T	0.396694	0.202437	intron-variant	Abtb2	Mm_Celera	2:103659635	AATTAATGTCAACTA[C/T]AGCACCAATGTCTCA	99382
rs27358175	snp	A/G	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103659489	CTCCCCTCAGCCCTG[A/G]CCACCACATGGACTG	99382
rs27358176	snp	C/G	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103659460	GAAGGTGAGATCTCA[C/G]GTAGAGCACACTGCT	99382
rs27358177	snp	C/T	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103659415	GTCTGAGAAGCCCCG[C/T]AGGTGAACACACAAC	99382
rs27358178	snp	A/T	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103659365	GAGATAAAGACAGAA[A/T]CTCAGTGTAGTCTTG	99382
rs27358179	snp	A/G	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103659195	CTATGGGTCTCTAGT[A/G]GGTCTTGGTCAGAAA	99382
rs27358180	snp	G/T	0.486111	0.0821678	intron-variant	Abtb2	GRCm38.p3	2:103659145	GTCTCTGGGAAAAAG[G/T]CCCATTCATACTGAG	99382
rs27358181	snp	A/G	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103659137	AGCTTTGAGTCTCTG[A/G]GAAAAAGGCCCATTC	99382
rs27358182	snp	A/G	0.486111	0.0821678	intron-variant	Abtb2	GRCm38.p3	2:103659123	GCTGGGTCTTGAGCA[A/G]CTTTGAGTCTCTGGG	99382
rs27358183	snp	A/G	0.375	0.216506	intron-variant	Abtb2	Mm_Celera	2:103659052	CTACACCCATTGACC[A/G]TCTCTGTGGAGAAGG	99382
rs27358184	snp	C/T	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103659024	GTTATGATTTTACTG[C/T]GAGCTGTCCATTCTA	99382
rs27358185	snp	C/T	0.42	0.183303	intron-variant	Abtb2	GRCm38.p3	2:103658515	TAATGTCACGTTAGA[C/T]ATCTCTACTTATGTG	99382
rs27358186	snp	A/G	0.497041	0.0383476	intron-variant	Abtb2	GRCm38.p3	2:103658323	ATATTAGAGTAAGAG[A/G]AAACATGAGGAAACT	99382
rs27358187	snp	C/T	0.5	0	intron-variant	Abtb2	GRCm38.p3	2:103658255	ATTTAAACACAGCCA[C/T]GGACTTTAAGACCCT	99382
rs27358188	snp	A/G	0.486111	0.0821678	intron-variant	Abtb2	GRCm38.p3	2:103658230	CTTTTTAAGGCCATG[A/G]CAGTTTCCAATTTAA	99382
rs27358189	snp	A/G	0.165289	0.235211	intron-variant	Abtb2	Mm_Celera	2:103658143	GTGCCTCTTTGTTCC[A/G]GATGTATGCTAAAGC	99382
rs27358190	snp	C/T	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103657993	CTATGCAGCAACGAG[C/T]CCTGATCTCATTTAT	99382
rs27358191	snp	A/T	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103657963	CACTCATAATAAGAA[A/T]GCCGAAAGCATCACC	99382
rs27358192	snp	A/C	0.492188	0.0620098	intron-variant	Abtb2	GRCm38.p3	2:103657822	CAAACAAAACCTATC[A/C]TCCTAGAAGCCAGCT	99382
rs27358193	snp	C/T	0.498615	0.0262793	intron-variant	Abtb2	GRCm38.p3	2:103657614	AGCCCAGAAATGCTG[C/T]TACTCACTGAGCATC	99382
rs27358194	snp	A/G	0.489796	0.070696	intron-variant	Abtb2	GRCm38.p3	2:103657513	GCCCCTGTTTTCCCA[A/G]CACCTCAAAATCTCT	99382
rs27358195	snp	A/G	0.336735	0.234472	intron-variant	Abtb2	GRCm38.p3	2:103657349	ACAGGTGAACCATTG[A/G]CTGGGTGCAAGAGCT	99382
rs27358196	snp	C/T	0.473373	0.11227	intron-variant	Abtb2	GRCm38.p3	2:103657219	GCAGCCCAACATCCT[C/T]ATTACATGACCTCAG	99382
rs27358197	snp	C/T	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103657172	GGACATGGGGCAGCA[C/T]TGTGGCAGGGCAGAG	99382
rs27358198	snp	A/G	0.336735	0.234472	intron-variant	Abtb2	GRCm38.p3	2:103657030	GCAAACCTTACTACA[A/G]ATTAGGCTGTCTATA	99382
rs27358200	snp	A/G	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103656655	GCTCATTCCTCTCCT[A/G]TAAGCTGGTGATGGG	99382
rs27358201	snp	A/T	0.408163	0.193609	intron-variant	Abtb2	GRCm38.p3	2:103656633	AGAATCTAGAACGGG[A/T]TGAACTGCTCATTCC	99382
rs27358202	snp	G/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103656605	CAGAAGAGTGTTCTG[G/T]CTCGGCGAAGGCAGA	99382
rs27358203	snp	G/T	0.21875	0.248039	intron-variant	Abtb2	Mm_Celera	2:103656598	TGGGCTTCAGAAGAG[G/T]GTTCTGTCTCGGCGA	99382
rs27358204	snp	A/G	0.497041	0.0383476	intron-variant	Abtb2	Mm_Celera	2:103656575	GAGAGGGTTGCGGAT[A/G]AGCAAGGTGGGCTTC	99382
rs27358205	snp	A/C/G	0.35503	0.226867	intron-variant	Abtb2	GRCm38.p3	2:103656571	AGAGGAGAGGGTTGC[A/C/G]GATAAGCAAGGTGGG	99382
rs27358206	snp	A/G	0.244898	0.249948	intron-variant	Abtb2	Mm_Celera	2:103656231	AGTCACTGTCCTGAT[A/G]CTTGAGACTGGGGTG	99382
rs27358207	snp	A/G	0.132653	0.220748	intron-variant	Abtb2	Mm_Celera	2:103656183	GGTTTTCCCTACACA[A/G]CCCTTTCTAGGCCCT	99382
rs27358208	snp	C/T	0.35503	0.226867	intron-variant	Abtb2	Mm_Celera	2:103656152	ACAGGGAATGGCAAA[C/T]ACACAGACAAGGTGG	99382
rs27358209	snp	G/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103656029	TGTACTCAGGACCAG[G/T]GCACTGGGTTGGGAT	99382
rs27358210	snp	A/G	0.336735	0.234472	intron-variant	Abtb2	Mm_Celera	2:103656015	GAGCTTCCTGTCTGT[A/G]TACTCAGGACCAGTG	99382
rs27358211	snp	C/T	0.336735	0.234472	intron-variant	Abtb2	Mm_Celera	2:103655973	GTCAGGATGGGACTA[C/T]GTGGGATGACTGCTG	99382
rs27358212	snp	A/G	0.336735	0.234472	intron-variant	Abtb2	Mm_Celera	2:103655946	CCTTTCCTGGAACAC[A/G]TGTGGCCTACAGTCA	99382
rs27358213	snp	G/T	0.336735	0.234472	intron-variant	Abtb2	Mm_Celera	2:103655835	AAGCCTGACAAACTG[G/T]CCTGTGTCACGTAAA	99382
rs27358214	snp	A/C	0.49827	0.0293608	intron-variant	Abtb2	GRCm38.p3	2:103655797	CTGCTTCCCTTTTCA[A/C]TGTGAGCTCTGAAAG	99382
rs27358215	snp	A/G	0.336735	0.234472	intron-variant	Abtb2	Mm_Celera	2:103655726	TGTGCCGGACTTTCA[A/G]TCTCTTTGTGCTGGT	99382
rs27358216	snp	A/G	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103655647	GGCCCAGGGTGCTGT[A/G]ACACGGTCACCCTGC	99382
rs27358217	snp	C/G	0.375	0.216506	intron-variant	Abtb2	Mm_Celera	2:103655283	GAAGTAGCCCAGGGT[C/G]AGCAGGTCATGACCT	99382
rs27358218	snp	C/T	0.459184	0.136902	intron-variant	Abtb2	GRCm38.p3	2:103655282	GGAAGTAGCCCAGGG[C/T]CAGCAGGTCATGACC	99382
rs27358219	snp	C/T	0.336735	0.234472	intron-variant	Abtb2	Mm_Celera	2:103655059	TCTCAGCACCTCAGT[C/T]AGCTTAGAGTCAGGC	99382
rs27358220	snp	A/G	0.336735	0.234472	intron-variant	Abtb2	Mm_Celera	2:103655015	GAATCATGACCACTG[A/G]AGACAAACAGCTACT	99382
rs27358221	snp	C/T	0.486111	0.0821678	intron-variant	Abtb2	Mm_Celera	2:103654972	TCCCCTCCCTGTCTC[C/T]CGTATGAAGAGAGAA	99382
rs27358222	snp	A/G	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103654910	ATCTGAGGAGACACA[A/G]GCAGAAGCAGGTGTT	99382
rs27358223	snp	A/G	0.132653	0.220748	intron-variant	Abtb2	Mm_Celera	2:103654867	ATAAGACATTGCACT[A/G]CAGGAAGGAGCCAAG	99382
rs27358224	snp	A/G	0.492188	0.0620098	intron-variant	Abtb2	GRCm38.p3	2:103654641	TAGCAGCAAAGGCTG[A/G]CCCTGAGTTCTCCCA	99382
rs27358225	snp	A/G	0.493827	0.0552116	intron-variant	Abtb2	GRCm38.p3	2:103654528	GTAGTGTTCAATTAA[A/G]CACGTTAGGTAAGAG	99382
rs27358226	snp	A/G	0.401235	0.199068	intron-variant	Abtb2	GRCm38.p3	2:103654425	GTACCAAGTCCAAGC[A/G]TAATGCTGAGACCTG	99382
rs27358227	snp	A/C	0.49827	0.0293608	intron-variant	Abtb2	GRCm38.p3	2:103654118	GCAATTTAGATTTAA[A/C]CCTTTGCACACTGGG	99382
rs27358228	snp	C/T	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103653865	TCTTAAAAGCCAAAC[C/T]ACAAGGAGATGAGGG	99382
rs27358229	snp	A/G	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103653808	AGGCTTTTTGTTGTA[A/G]TAGGACTCAAACAAG	99382
rs27358230	snp	A/C	0.497778	0.0332592	intron-variant	Abtb2	GRCm38.p3	2:103653749	TGATCTGTTGAGCAT[A/C]CCAGGCTCATTTCAA	99382
rs27358231	snp	C/T	0.132653	0.220748	intron-variant	Abtb2	Mm_Celera	2:103653290	CAGGGCCTGTTTTGT[C/T]CACCTTCAGTAAAGT	99382
rs27358232	snp	C/T	0.132653	0.220748	intron-variant	Abtb2	Mm_Celera	2:103653197	CTAAATTCCTTAGCG[C/T]CCTGGTCTGTAGTTA	99382
rs27358233	snp	A/C	0.415225	0.187619	intron-variant	Abtb2	GRCm38.p3	2:103653195	TGCTAAATTCCTTAG[A/C]GCCCTGGTCTGTAGT	99382
rs27358234	snp	C/T	0.401235	0.199068	intron-variant	Abtb2	GRCm38.p3	2:103653171	TTGAGAGGCTTGTGT[C/T]AAGTGGTGTGCTAAA	99382
rs27358235	snp	A/C	0.244898	0.249948	intron-variant	Abtb2	Mm_Celera	2:103653159	TTCACTCAGTTTTTG[A/C]GAGGCTTGTGTCAAG	99382
rs27358236	snp	C/G	0.484429	0.0868505	intron-variant	Abtb2	GRCm38.p3	2:103653074	AAGATCCTGAAAACT[C/G]AACACATTTCTCTTG	99382
rs27358237	snp	A/G	0.132653	0.220748	intron-variant	Abtb2	Mm_Celera	2:103652679	ATGTGGGCTTCCGCA[A/G]TGGGTTCATGGTTGA	99382
rs27358238	snp	A/T	0.132653	0.220748	intron-variant	Abtb2	Mm_Celera	2:103652134	CCACACTTGTGAGTT[A/T]ATTTGCGTGTGTGTG	99382
rs27358239	snp	A/G	0.336735	0.234472	intron-variant	Abtb2	Mm_Celera	2:103651707	AGCTATGGACACCTT[A/G]ATTCTCATGTGGCCT	99382
rs27358240	snp	A/G	0.401235	0.199068	intron-variant	Abtb2	GRCm38.p3	2:103651571	CAGTTCTTCTTCTGG[A/G]AACTCCTTAAGTTGT	99382
rs27358241	snp	A/G	0.336735	0.234472	intron-variant	Abtb2	GRCm38.p3	2:103651119	AGGCTCTCTGAAACC[A/G]GAATATAGAATGCTC	99382
rs27358242	snp	A/G	0.497041	0.0383476	intron-variant	Abtb2	GRCm38.p3	2:103650965	CCTGCATGGAGGCAG[A/G]AGTCAGTGATGCCCT	99382
rs27358243	snp	C/T	0.408163	0.193609	intron-variant	Abtb2	GRCm38.p3	2:103650719	CTTTTCCCGGTATAC[C/T]TGATGCCTGTTGGTA	99382
rs27358244	snp	A/G	0.49827	0.0293608	intron-variant	Abtb2	GRCm38.p3	2:103650236	TATGAGCCTTTTGTG[A/G]CAGATGCTTGAGACT	99382
rs27358245	snp	A/C	0.244898	0.249948	intron-variant	Abtb2	Mm_Celera	2:103650186	TTTCCTCTGGCATTG[A/C]GTGTTGCATGCAAGT	99382
rs27358246	snp	C/T	0.484429	0.0868505	intron-variant	Abtb2	GRCm38.p3	2:103650175	CCATCTTGGGCTTTC[C/T]TCTGGCATTGCGTGT	99382
rs27358247	snp	A/G	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103650053	GTTCTGGCCTCACAC[A/G]CATGTATACACATGT	99382
rs27358248	snp	A/G	0.244898	0.249948	intron-variant	Abtb2	Mm_Celera	2:103649653	ATCTCTGATCTCCAT[A/G]TCTTGCATGTTAATG	99382
rs27358249	snp	C/T	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103649432	TAACTTGAGTTTGAG[C/T]TTTGTCTAAGGAGGA	99382
rs27358250	snp	C/T	0.244898	0.249948	intron-variant	Abtb2	Mm_Celera	2:103649391	TGACTTTAACTTCTG[C/T]CCCATTTCCCTTATG	99382
rs27358251	snp	C/T	0.336735	0.234472	intron-variant	Abtb2	Mm_Celera	2:103649308	AGGTTTCAGAATGTC[C/T]TCAGAGCCACTGTGG	99382
rs27358252	snp	C/G	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103649280	ATAACCAGGAATTAG[C/G]TTTCATTTAAGCAGG	99382
rs27358253	snp	C/T	0.415225	0.187619	intron-variant	Abtb2	GRCm38.p3	2:103649141	TGTCCCAGCTGAAAT[C/T]AGAAACTGGCAGTGG	99382
rs27358254	snp	A/G	0.244898	0.249948	intron-variant	Abtb2	Mm_Celera	2:103649109	TTCAGTAGATTATAA[A/G]CTGACCCTAGTGTAG	99382
rs27358255	snp	C/T	0.415225	0.187619	intron-variant	Abtb2	GRCm38.p3	2:103649037	GCTTTATTGAATTCA[C/T]GTTTTCTGGGTGTCT	99382
rs27358256	snp	C/T	0.429688	0.173817	intron-variant	Abtb2	Mm_Celera	2:103648996	ACTGGTCGCTAGTGG[C/T]TGGCAATGATTTATT	99382
rs27358257	snp	A/C	0.260355	0.249785	intron-variant	Abtb2	GRCm38.p3	2:103648947	ACCCTCACCCGGAGC[A/C]AGAGTTGGGAACAAA	99382
rs27358258	snp	A/G	0.493827	0.0552116	intron-variant	Abtb2	GRCm38.p3	2:103648656	TGTCACACTGCACAG[A/G]TCGCTGACACCCAGT	99382
rs27358259	snp	A/G	0.336735	0.234472	intron-variant	Abtb2	Mm_Celera	2:103648577	AAAACGTCATTGGCA[A/G]TTTTGCCTTGAGTGT	99382
rs27358260	snp	G/T	0.244898	0.249948	intron-variant	Abtb2	Mm_Celera	2:103648056	TTTGCTCCTGCAGCC[G/T]TATAGCTATGAGAGT	99382
rs27358261	snp	A/G	0.132653	0.220748	intron-variant	Abtb2	Mm_Celera	2:103647811	CAACCTAGCAGGACC[A/G]TGACAATTTCTCTTC	99382
rs27358262	snp	A/G	0.244898	0.249948	intron-variant	Abtb2	Mm_Celera	2:103647779	GGTCAGTCTTGAGAC[A/G]CATCTTTGTAACAAG	99382
rs27358263	snp	C/T	0.244898	0.249948	intron-variant	Abtb2	Mm_Celera	2:103647630	GTTCCTCCCAGAAGA[C/T]GCCTGGAGATTGAGT	99382
rs27358264	snp	A/C	0.244898	0.249948	intron-variant	Abtb2	Mm_Celera	2:103647597	CTTCTAGCCTAAATA[A/C]TCCCTTTACCTCTTT	99382
rs27358265	snp	A/C	0.244898	0.249948	intron-variant	Abtb2	Mm_Celera	2:103647554	ATCACAGCAAGTTTG[A/C]CCTTTCCTGGCCTGG	99382
rs27358266	snp	A/C	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103647499	AAGAAGCAATCATTA[A/C]TAATACTCACACTAG	99382
rs27358267	snp	A/G	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103647131	CCTAACTACTCTAAA[A/G]TAGAGGAAAAGGCAG	99382
rs27358268	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103646964	TTTGGAGCATGCATT[A/G]GCGGTGGTGCTCAGA	99382
rs27358269	snp	A/C	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103646770	TAAAATGAAGTTGAG[A/C]GCCAAAGCAGAGCTA	99382
rs27358270	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103646721	CTAACACACTCCTGT[A/G]AGTTAAGCTCCACAA	99382
rs27358271	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103646699	GGTCAAGAGTCTGCA[A/G]ATTGCCCTAACACAC	99382
rs27358272	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103646677	AGTGGATGAAAATAA[C/T]TAGGTGGGTCAAGAG	99382
rs27358273	snp	A/G	0.498615	0.0262793	intron-variant	Abtb2	GRCm38.p3	2:103646333	TGAAAAGTACTGATA[A/G]CCTATGCATTCAGGT	99382
rs27358274	snp	A/G	0.498615	0.0262793	intron-variant	Abtb2	GRCm38.p3	2:103646130	AGCACAGGATGGTGC[A/G]TCTCATTCTGACCTT	99382
rs27358275	snp	A/G	0.456747	0.140554	intron-variant	Abtb2	GRCm38.p3	2:103646116	GCAGAAAGTATCTCA[A/G]CACAGGATGGTGCAT	99382
rs27358276	snp	A/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103645727	TTAGTAAATTCTTTC[A/T]AAGAAGCTGTTCTGA	99382
rs27358277	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103645692	GATTGCTTGAAGTAA[A/G]TCCACAAAATAAGTA	99382
rs27358278	snp	A/G	0.415225	0.187619	intron-variant	Abtb2	Mm_Celera	2:103645610	CCTCACCCTTTCCTA[A/G]CTCTGGGCAGGATAC	99382
rs27358279	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103645479	AAGTGTTTTGCAAAG[C/T]CTTATTTAGATAAAA	99382
rs27358280	snp	G/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103645422	TTTGCAGAAAATCTT[G/T]TAGGTTACTCAACTT	99382
rs27358281	snp	C/G/T	0.497041	0.0383476	intron-variant	Abtb2	GRCm38.p3	2:103645323	TTGGTCCTAACTGTT[C/G/T]CTAGGTTACCTAAAA	99382
rs27358282	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103645296	AGCTCTATCTTCCAT[A/G]CAAACCTGATCTTGG	99382
rs27358283	snp	A/G	0.498615	0.0262793	intron-variant	Abtb2	Mm_Celera	2:103645179	AATCCAAAAACTTGG[A/G]AGATGCAGGTTTTTA	99382
rs27358284	snp	A/G	0.498615	0.0262793	intron-variant	Abtb2	GRCm38.p3	2:103644821	TATCCACAAGTCTAC[A/G]TGCATCAACTCATCA	99382
rs27358285	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103644397	GCCTTGAACCTGCTG[C/T]ATGTCTGGATAGCAG	99382
rs27358286	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103644207	CTTGTAAAATTTTCC[A/G]TCTTTAGAGGAGGTG	99382
rs27358287	snp	A/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103644157	AGTAATTCTTGGATC[A/T]GGCAGTGCAGTGTGA	99382
rs27358288	snp	A/C	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103644041	ATTGGAAGATGCCCG[A/C]AGCTTCACTCTGCAT	99382
rs27358289	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103643965	ATGGAGGAAGAAAAG[C/T]CCAACCAGAAAGCAT	99382
rs27358290	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103643657	TGGTTCCTCTCAGTC[C/T]GATTTTCAGGGCTAT	99382
rs27358291	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103643517	CTCGCAAGGCATTTA[A/G]CATTCAGGCCTCTAA	99382
rs27358292	snp	A/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103643501	CTGATGCTACAGCAG[A/T]CTCGCAAGGCATTTA	99382
rs27358293	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103642231	TACCTCAGAATGCCA[C/T]GGATACACACACACA	99382
rs27358294	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103642103	GTGAGTTGTTTATCA[A/G]TGTGGAGGGAAGGGA	99382
rs27358295	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103642066	AGAGTAGCAGGTGAT[A/G]GAAAAAGCAAAGCCT	99382
rs27358296	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103641987	TAACTCATTCCTACA[A/G]CTGTCCAGCTTCCCA	99382
rs27358297	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103641914	CCTTCTGCATCTAGA[C/T]TTGATCTGTGTTCTC	99382
rs27358298	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103641782	ATGGAGAATTGTCCT[C/T]AGCCTCCTAACAGAG	99382
rs27358299	snp	A/C	0.401235	0.199068	intron-variant	Abtb2	GRCm38.p3	2:103641624	CGAACCCTGATGGCA[A/C]CGGGACTCCCTCCAC	99382
rs27358300	snp	C/G	0.277778	0.248452	intron-variant	Abtb2	Mm_Celera	2:103641538	ATGGTAGACTCACAG[C/G]CTGAGCCCCATGCCC	99382
rs27358301	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103641515	GAGTGCTAGGGAGAG[C/T]CAGACCCATGGTAGA	99382
rs27358302	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103641428	TCACTTCAGCATAGA[C/T]CTGAGAGGCCATTTA	99382
rs27358303	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103641416	GGACCCATGATCTCA[C/T]TTCAGCATAGATCTG	99382
rs27358304	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103641367	CTGACTGTACTGACC[C/T]GATGGCCTCTCTTCT	99382
rs27358305	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103641138	ATTGGTTTTGAGCTT[C/T]TCTGTGGGTTTCTTT	99382
rs27358306	snp	G/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103641087	CTCTAGAAATGACTG[G/T]TCCAGAACAAAGAGG	99382
rs27358307	snp	C/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103641060	CCTGGGCCTACCTCG[C/G]ACAGTTCAGTGCTCT	99382
rs27358308	snp	G/T	0.497778	0.0332592	intron-variant	Abtb2	GRCm38.p3	2:103641057	CACCCTGGGCCTACC[G/T]CGCACAGTTCAGTGC	99382
rs27358309	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103640738	GGCCAGGTACCCTTT[C/T]TTCTGTTCGCTTTTA	99382
rs27358310	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103640556	GGAAGGTAAAGAGCC[C/T]GACCAGGATGCCTGG	99382
rs27358311	snp	G/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103640426	TGTGGACTGAGAACC[G/T]TTCTTGGTATCTCCC	99382
rs27358312	snp	A/G/T	0.244898	0.249948	intron-variant	Abtb2	Mm_Celera	2:103640255	AGGAAGGATAAGGCT[A/G/T]CTCTGAAATCCCATG	99382
rs27358313	snp	C/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103640184	TACACAGCACCAGGG[C/G]TAGAAGGGCTCAGTC	99382
rs27358314	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103639918	GGAAATGAAGGCATC[C/T]TCCCAGGAGCACAGT	99382
rs27358315	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103639581	GGTTGACAGTGTCTG[A/G]TAGTTGTCCATACAA	99382
rs27358316	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103639386	GTTGTGAGGGGCTTT[C/T]GGAAAGTCAACAAGA	99382
rs27358317	snp	A/G	0.46875	0.121031	intron-variant	Abtb2	GRCm38.p3	2:103639277	CTGGGGTAGAAATGT[A/G]AAAGAGAGTCAGGTA	99382
rs27358318	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103639230	TAGCTGTCTGTCCAC[C/T]CAAGCATGTTCAGGA	99382
rs27358319	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103639195	AGCATCATTATCACA[C/T]GGAAAAACACTGTAA	99382
rs27358320	snp	C/G	0.5	0	intron-variant	Abtb2	GRCm38.p3	2:103638962	CAAGTTGCTGGGAAA[C/G]AGCAGCCCCCAGTAA	99382
rs27358321	snp	C/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103638953	ACATCCAGACAAGTT[C/G]CTGGGAAACAGCAGC	99382
rs27358322	snp	C/T	0.391111	0.206368	intron-variant	Abtb2	Mm_Celera	2:103638702	ACCCATCATGGAAGG[C/T]GATTTGTAAGGACAG	99382
rs27358323	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103638620	AGAAACTGACAAGAG[A/G]GAGCTGTCATCTTCT	99382
rs27358324	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103638267	TACATAGCTGCTCCT[A/G]TGATCAGCCTGGGTG	99382
rs27358325	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103638182	AAAAGAGAAGAGCCT[A/G]TTCCTGTCACAGTGG	99382
rs27358326	snp	A/G	0.391111	0.206368	intron-variant	Abtb2	GRCm38.p3	2:103638090	GGTCTCACGCTTCGG[A/G]CTCTGGCTGGGGGCA	99382
rs27358327	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103637939	AGAAGGGACCAGTGC[C/T]CATGTTCTCTTCAGA	99382
rs27358328	snp	A/C	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103637539	GTGTTTCCAGCTGTG[A/C]AGTTGAGAGGGAGAT	99382
rs27358329	snp	A/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103636904	CCCAATTGCTTCAGA[A/T]TTCCTGGGACAGTCA	99382
rs27358330	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103636746	GAACTTGCCAGGCCT[A/G]GTGACCCAGAACCCC	99382
rs27358331	snp	A/C	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103636673	AGCATGTAGTTGTTA[A/C]CCCTGATAGAGATGG	99382
rs27358332	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103636489	CAACGCATGGTACAG[C/T]GTGGATGTCTGTGGA	99382
rs27358333	snp	C/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103636348	GTTTCTTGTTTCTCT[C/G]TGTTACCACTCCATC	99382
rs27358334	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103636181	TTGTGACAAGGTATT[A/G]TCAAGTTCAATTTAG	99382
rs27358335	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103635881	CCAAAACTAAGATGC[C/T]GTGGTGTCACCAGGA	99382
rs27358336	snp	A/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103635804	ATAAGTACCTGGTAT[A/T]GGATCTGAGCAGTAT	99382
rs27358337	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103635649	ATAGTTGTGAACTCA[C/T]TAGTCAAATCCTCTG	99382
rs27358338	snp	A/G	0.132653	0.220748	intron-variant	Abtb2	Mm_Celera	2:103635636	CATGAGGGATGACAT[A/G]GTTGTGAACTCACTA	99382
rs27358339	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103635481	CAGTGAAGGCCGTTA[A/G]CATCAATGAGAAGCA	99382
rs27358340	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103635243	GAACCCAGACAGTCT[A/G]GAATTCACACTTTTT	99382
rs27358341	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103634885	ACAATTAAAGCAGAC[C/T]CCTGGTGTCTCCTTG	99382
rs27358342	snp	G/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103634751	AGCTTAGTCTCCAAA[G/T]CAGTGAGCTAGAAGC	99382
rs27358343	snp	A/G	0.432133	0.171253	intron-variant	Abtb2	GRCm38.p3	2:103634736	TCCATGTCCCTTGCT[A/G]GCTTAGTCTCCAAAG	99382
rs27358344	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103634427	TAAGTTCTTAGGAAG[C/T]TTGATCTTGAAGCTA	99382
rs27358345	snp	G/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103634325	CCCATAGCAACTGAT[G/T]GAGTGATGTCCTCCA	99382
rs27358346	snp	A/G	0.336735	0.234472	intron-variant	Abtb2	Mm_Celera	2:103633977	GCAGCATTATTAATA[A/G]AAGGCAAAGCAAGAA	99382
rs27358347	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103633937	ACTGGAAAAGCAATA[A/G]ACAGAATAAGCCAGC	99382
rs27358348	snp	A/G	0.498615	0.0262793	intron-variant	Abtb2	GRCm38.p3	2:103633110	AATGTATTCCAAATG[A/G]TGGAATCTGATTTTT	99382
rs27358349	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103633072	CAGGTCTTGAGTAAG[A/G]ATGCTGTCTCGGACC	99382
rs27358350	snp	C/T	0.35503	0.226867	intron-variant	Abtb2	Mm_Celera	2:103632996	TGAGGTAAGGGCATG[C/T]TGGTAACTCAGACTC	99382
rs27358351	snp	A/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103632974	TTTATTTACAGCCCC[A/T]AGTCAATGAGGTAAG	99382
rs27358352	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103632765	TCTAGGCAGGAAATC[A/G]AAGATCGGATTGCTG	99382
rs27358353	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103632664	AGGTGTGGAGCTAGG[A/G]GCCACCTAAGTGGAG	99382
rs27358354	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103632623	CATACCACTGCAAAC[A/G]CAGATGAAAGGTGAT	99382
rs27358355	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103632570	CCTTAGCATACAGTG[C/T]GCAATTAACTCTGCT	99382
rs27358356	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103632534	ATGCTTGGCATGAAA[A/G]GCAGGCAGTGTGTGA	99382
rs27358357	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103632450	CCTCAGATGTCAAGG[C/T]CATGCCCAGCTGTCC	99382
rs27358358	snp	A/G	0.497041	0.0383476	intron-variant	Abtb2	GRCm38.p3	2:103632308	TAGTTCTTAGAAGTT[A/G]GTGAGCTGATGAATT	99382
rs27358359	snp	A/T	0.486111	0.0821678	intron-variant	Abtb2	Mm_Celera	2:103632301	TTGTTTCTAGTTCTT[A/T]GAAGTTGGTGAGCTG	99382
rs27358360	snp	A/C	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103632265	AGGGCAAAGCCTTCC[A/C]ACACTGGTGACACCT	99382
rs27358361	snp	A/C	0.244898	0.249948	intron-variant	Abtb2	GRCm38.p3	2:103632025	CATAAGAAATAAAAT[A/C]CCCCGGGGCTGGTGA	99382
rs27358362	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103632005	GGTATCATTCAGGAG[C/T]CTCCCATAAGAAATA	99382
rs27358363	snp	C/T	0.489796	0.070696	intron-variant	Abtb2	GRCm38.p3	2:103631951	CATGACTCTGCAATG[C/T]TGCATTTCTCCTGTC	99382
rs27358364	snp	C/T	0.5	0	intron-variant	Abtb2	Mm_Celera	2:103631942	GGGGTTTGACATGAC[C/T]CTGCAATGCTGCATT	99382
rs27358365	snp	C/T	0.497778	0.0332592	intron-variant	Abtb2	GRCm38.p3	2:103631829	AAATAACTGATTAAA[C/T]CCAGGGGAGAAGAAA	99382
rs27358366	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103631716	GGTATGTATAGCCAA[A/G]TAGAAGTTTGTGTAT	99382
rs27358367	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103631557	GACTTGTCAAGTGCC[A/G]TAACCCTAAGCAGTA	99382
rs27374868	snp	A/G	0.498615	0.0262793	intron-variant	Abtb2	GRCm38.p3	2:103631273	GCCTGGCCGTGCAGT[A/G]GAAATCAGGATGCAT	99382
rs27374869	snp	A/G	0.498615	0.0262793	intron-variant	Abtb2	GRCm38.p3	2:103631246	GACACATTTAAGAAT[A/G]CAGGCGTCTTTGCCT	99382
rs27374870	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103631229	TGGAATTGCTTTGAC[A/G]AGACACATTTAAGAA	99382
rs27374871	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103631215	AGCTGCCTTGAAAGT[A/G]GAATTGCTTTGACGA	99382
rs27374872	snp	C/T	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103630859	AAAGCACTCAGGGTA[C/T]CCTTACAAATCCACT	99382
rs27374873	snp	G/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103630791	GGAAAATGAAATTCA[G/T]ACGACCCTTTCTTTT	99382
rs27374874	snp	A/C	0.495868	0.0452663	intron-variant	Abtb2	GRCm38.p3	2:103630725	ACAAGCATTACGTGA[A/C]TATTAACAAAAGATA	99382
rs27374875	snp	A/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103630400	CTAAGAACCTAAGCA[A/T]CAATTAATCCCCAAC	99382
rs27374876	snp	A/G	0.132653	0.220748	intron-variant	Abtb2	Mm_Celera	2:103630346	CTACAGGAAATCAAA[A/G]TAGAGCCTTATCAGT	99382
rs27374877	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103630299	TTCCCCCTGCAGAAC[A/G]GTGATGCCGACAAGC	99382
rs27374878	snp	A/G	0.5	0	intron-variant	Abtb2	GRCm38.p3	2:103630264	CCAGCACACAGCCGC[A/G]CATGTACATTTACTT	99382
rs27374879	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103630151	TGCCTCTATAGAGGC[A/G]GGCATCTTTGGACAT	99382
rs27374880	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103630025	GGATATGAAGGGGAA[A/G]GCAGACGGCCTGTAC	99382
rs27374881	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103629941	GGGACTTCATGCACC[C/T]GTTCAGATTTCATTT	99382
rs27374882	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103629810	GGAGTTACAGGGGGA[A/G]TGAAAGATTGTGTTG	99382
rs27374883	snp	A/C	0.231111	0.249285	intron-variant	Abtb2	GRCm38.p3	2:103629752	AATGTTCTAAGCCCT[A/C]ACTTCCTTCTCTGTG	99382
rs27374884	snp	C/T	0.493827	0.0552116	intron-variant	Abtb2	GRCm38.p3	2:103629611	ATCTGAAATCTCATC[C/T]CAACTAATTCCGTTC	99382
rs27374885	snp	G/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103629551	GCTCCCTAGTCGCCC[G/T]CCTTCCTTTTTGGTA	99382
rs27374886	snp	A/T	0.49827	0.0293608	intron-variant	Abtb2	GRCm38.p3	2:103629431	CAGGAAAGGCTATGC[A/T]GAGTGGGCACAGGGA	99382
rs27374887	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103629384	CTCAGGCAGTTCTCA[A/G]AGGTGAGAAGACTGG	99382
rs27374888	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103629157	GTCTGAGGCTTGAGC[A/G]GGTGTGCTAGCCAGA	99382
rs27374889	snp	G/T	0.48	0.0979796	intron-variant	Abtb2	GRCm38.p3	2:103629081	GTATCGATGGTTTCA[G/T]GTCCAGAGGCTTTGC	99382
rs27374890	snp	A/G	0.396694	0.202437	intron-variant	Abtb2	Mm_Celera	2:103629056	AAAGGTTACGCAGAG[A/G]GCAGAGAGAGTATCG	99382
rs27374891	snp	A/G	0.497778	0.0332592	intron-variant	Abtb2	GRCm38.p3	2:103628992	TTGAAGAAAACAAAC[A/G]ATTTGGGCTTTGGAA	99382
rs27374892	snp	C/G	0.459184	0.136902	intron-variant	Abtb2	GRCm38.p3	2:103628957	TTGTAGCAAATAGCT[C/G]TTGTTACTCATTAGT	99382
rs27374893	snp	A/C	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103628935	TGGACTCATTGGTGC[A/C]GCTTCATTGTAGCAA	99382
rs27374894	snp	C/G/T	0.124444	0.216185	intron-variant	Abtb2	GRCm38.p3	2:103628855	GAAGAGAGTTGGCTC[C/G/T]ATCCTGGAGTGCAGT	99382
rs27374895	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103628738	CTTCCACAGTCTAAA[A/G]ATGCACCATTTGGCT	99382
rs27374896	snp	A/G	0.489796	0.070696	intron-variant	Abtb2	GRCm38.p3	2:103627926	CTGTATCGCTGTGGA[A/G]TTAATATGTCCTCCC	99382
rs27374897	snp	C/T	0.48	0.0979796	intron-variant	Abtb2	GRCm38.p3	2:103627917	CAAGATGTCCTGTAT[C/T]GCTGTGGAATTAATA	99382
rs27374898	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103627895	TCTTGCAAGGTGTTT[C/T]ATTATACAAGATGTC	99382
rs27374899	snp	C/T	0.497778	0.0332592	intron-variant	Abtb2	GRCm38.p3	2:103627660	TGTTTTCACTGAGCA[C/T]ACCTTTTTAACTCAA	99382
rs27374900	snp	A/G	0.48	0.0979796	intron-variant	Abtb2	Mm_Celera	2:103627135	ATATGTTAAATGGGC[A/G]TGTGCCCTGATTTAA	99382
rs27374901	snp	A/T	0.48	0.0979796	intron-variant	Abtb2	Mm_Celera	2:103627061	TTATGAATGAGATGG[A/T]TTTTACACACACATA	99382
rs27374902	snp	C/G/T	0.48	0.0979796	intron-variant	Abtb2	GRCm38.p3	2:103627009	ATTTTTTGTCTTGAC[C/G/T]TGTGTTCTAAATTAC	99382
rs27374903	snp	C/T	0.132653	0.220748	intron-variant	Abtb2	Mm_Celera	2:103626696	AGGCAAGAAAGGTCC[C/T]TGTAGAATTACTAAG	99382
rs27374904	snp	A/G	0.473373	0.11227	intron-variant	Abtb2	GRCm38.p3	2:103626688	GTAAATCCAGGCAAG[A/G]AAGGTCCTTGTAGAA	99382
rs27374905	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103626628	ACGGAGACAACAGCA[C/T]ATGGGTTCAAGTGTG	99382
rs27374906	snp	A/G	0.277778	0.248452	intron-variant	Abtb2	Mm_Celera	2:103626618	CAGAACCTACACGGA[A/G]ACAACAGCACATGGG	99382
rs27374907	snp	G/T	0.497778	0.0332592	intron-variant	Abtb2	GRCm38.p3	2:103626615	TAGCAGAACCTACAC[G/T]GAGACAACAGCACAT	99382
rs27374908	snp	A/G	0.497778	0.0332592	intron-variant	Abtb2	GRCm38.p3	2:103626408	TCCTAGATAGTGGCA[A/G]TGTCCCAGGTTTTGT	99382
rs27374909	snp	C/T	0.497778	0.0332592	intron-variant	Abtb2	GRCm38.p3	2:103626373	GATGCTAAGAGTCTC[C/T]CAAAAGCTGAGCAAT	99382
rs27374910	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103626335	TGTTTAGGTCCCTTA[C/T]TAATTGGTCACTAGT	99382
rs27374911	snp	C/T	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103626196	CTGGGTACCTAATGG[C/T]GATTCTGGTTATCTA	99382
rs27374912	snp	A/G	0.48	0.0979796	intron-variant	Abtb2	GRCm38.p3	2:103626145	TATCTTTCCCATTCC[A/G]TTTCTGAATAGAATC	99382
rs27374913	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103626118	AATTACTGTCTGGGC[A/G]TGGCTTACAAATATC	99382
rs27374914	snp	C/T	0.48	0.0979796	intron-variant	Abtb2	Mm_Celera	2:103626032	CAAGTTGCTTCTTTC[C/T]GAGTGGGACTTTACC	99382
rs27374915	snp	A/G	0.48	0.0979796	intron-variant	Abtb2	Mm_Celera	2:103625874	TCAAGTGGGGTGTGC[A/G]CAAACACAGAGCCTG	99382
rs27374916	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103625439	AGCTACTCAGTCCTG[C/T]TAGAGTCACCAGCCA	99382
rs27374917	snp	A/C	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103625099	GTGTGACAGCATCAA[A/C]GGGCAAGGCAGTAAG	99382
rs27374918	snp	A/G	0.375	0.216506	intron-variant	Abtb2	Mm_Celera	2:103624878	TTTAGCTTAGCAGCA[A/G]AAGAAACAATAGCAT	99382
rs27374919	snp	C/T	0.297521	0.245442	intron-variant	Abtb2	Mm_Celera	2:103624723	CTCCTTTATTTTTCT[C/T]CCAAGAAACCTTCAG	99382
rs27374920	snp	A/G	0.297521	0.245442	intron-variant	Abtb2	Mm_Celera	2:103624523	ACATGGAGAGAATAA[A/G]GGTTAAAAGGCTTTT	99382
rs27374921	snp	A/T	0.297521	0.245442	intron-variant	Abtb2	Mm_Celera	2:103624245	TGCTGCATACATTTT[A/T]AAAAATTGCCTTTTG	99382
rs27374922	snp	A/C	0.197531	0.244432	intron-variant	Abtb2	Mm_Celera	2:103624075	GATGGAAAGGATCTC[A/C]ATGTCAGGTAGTGCT	99382
rs27374923	snp	C/T	0.396694	0.202437	intron-variant	Abtb2	Mm_Celera	2:103623990	CTGATGCTCACATGG[C/T]GGGCTCTGGAAAGCT	99382
rs27374924	snp	C/T	0.297521	0.245442	intron-variant	Abtb2	Mm_Celera	2:103623657	TTCTTTATGCTTACT[C/T]ATTCCATTTTGAGCA	99382
rs27374925	snp	C/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103623556	TACATAAAGTGTTTG[C/G]AAGTTTATAAAAGAC	99382
rs27374926	snp	G/T	0.297521	0.245442	intron-variant	Abtb2	Mm_Celera	2:103623285	AGGAACACCACTATT[G/T]CAAATCTTCTATTAT	99382
rs27374927	snp	A/G	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103623267	ATATTCAGAAAACAT[A/G]GGAGGAACACCACTA	99382
rs27374928	snp	A/G	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103623054	CACACAGAAGCCTGG[A/G]TGTAATGAGAAGGGC	99382
rs27374929	snp	A/T	0.375	0.216506	intron-variant	Abtb2	Mm_Celera	2:103622865	CTGTTCCATGTCAAA[A/T]AATTGGGATTAGTGT	99382
rs27374930	snp	A/C	0.444444	0.157135	intron-variant	Abtb2	Mm_Celera	2:103622773	CAGCGTCCAGTGTAT[A/C]GTTCGAAGGATTAAT	99382
rs27374931	snp	A/C	0.165289	0.235211	intron-variant	Abtb2	Mm_Celera	2:103622623	TCTCTGAGTTTACAA[A/C]GACAAAAACAACCAT	99382
rs27374932	snp	C/T	0.375	0.216506	intron-variant	Abtb2	Mm_Celera	2:103622386	TGTAACTTTCACAGA[C/T]ATTGTAACTCTTAGA	99382
rs27374933	snp	A/G	0.375	0.216506	intron-variant	Abtb2	Mm_Celera	2:103620618	GCCTACTACCAGAGC[A/G]GCACCCAAATTTTAG	99382
rs27374934	snp	A/G	0.297521	0.245442	intron-variant	Abtb2	Mm_Celera	2:103620511	CCTATCTTTAGGGCT[A/G]TATTAAACATGACTT	99382
rs27374935	snp	A/G	0.297521	0.245442	intron-variant	Abtb2	Mm_Celera	2:103620477	GCCTTGCCAATTGGT[A/G]TAAGTGTATGAGCCT	99382
rs27374936	snp	A/G	0.375	0.216506	intron-variant	Abtb2	GRCm38.p3	2:103620287	GCTGCTGAGCTAGAG[A/G]TTTGTTGAGTTCAGT	99382
rs27374937	snp	C/T	0.165289	0.235211	intron-variant	Abtb2	Mm_Celera	2:103618754	AAATGCTATTTTTTT[C/T]CCTCAGTTGGTCTTA	99382
rs27374938	snp	C/G	0.486111	0.0821678	intron-variant	Abtb2	GRCm38.p3	2:103618645	AATGACTGGACTCCA[C/G]TCTCTCTGACACTTA	99382
rs27374939	snp	A/C	0.165289	0.235211	intron-variant	Abtb2	Mm_Celera	2:103618216	TTTTGCTCAACCAAA[A/C]TCAGCCCATTTGTGT	99382
rs27374940	snp	A/C	0.197531	0.244432	intron-variant	Abtb2	Mm_Celera	2:103618178	TCTATTAACCATAAA[A/C]ACAGACTTTGCTTTT	99382
rs27374941	snp	G/T	0.46875	0.121031	intron-variant	Abtb2	Mm_Celera	2:103617371	CATTATAAGAAGTAC[G/T]CTTTGGGCTGGTGAG	99382
rs27374942	snp	C/G	0.48	0.0979796	intron-variant	Abtb2	Mm_Celera	2:103617130	CTACTTTATGGGGCA[C/G]ATGGATGTGTGACTC	99382
rs27374943	snp	C/T	0.46281	0.131194	intron-variant	Abtb2	Mm_Celera	2:103616499	TCCCTGAGGGTCCTC[C/T]TCTTTGCCTAGGTCC	99382
rs27374944	snp	A/G	0.495868	0.0452663	intron-variant	Abtb2	Mm_Celera	2:103616349	TAACCCCCTTGCCCT[A/G]CTTCTCTCGCTCCAT	99382
rs27374945	snp	A/T	0.444444	0.157135	intron-variant	Abtb2	Mm_Celera	2:103616101	GTTTCTGTTTTGGGA[A/T]TTAGGCTGTTCAGTT	99382
rs27374946	snp	A/T	0.375	0.216506	intron-variant	Abtb2	Mm_Celera	2:103616063	CATGTTGACACTCAA[A/T]CTTGGATTTTGGAGG	99382
rs27374947	snp	A/G	0.42	0.183303	intron-variant	Abtb2	Mm_Celera	2:103615382	CACAGGGAAGCCCAG[A/G]GAAAGCATGGTTAGA	99382
rs27374948	snp	A/C	0.426035	0.177515	intron-variant	Abtb2	Mm_Celera	2:103614620	TGATTGGAATCACTT[A/C]GCATGAGTGCCGTAG	99382
rs27374949	snp	A/G	0.5	0	intron-variant	Abtb2	Mm_Celera	2:103614584	ACCTCAGCATGACTG[A/G]AGAGGAGCATTCACA	99382
rs27374950	snp	C/G	0.396694	0.202437	intron-variant	Abtb2	Mm_Celera	2:103614489	CCCATCGTTTGCCCT[C/G]ACTTTCCACTACATT	99382
rs27374951	snp	C/T	0.396694	0.202437	intron-variant	Abtb2	Mm_Celera	2:103614459	TTGCTTCTCTCCTCA[C/T]TTAAGAGATCTCAGC	99382
rs27374952	snp	A/G	0.444444	0.157135	intron-variant	Abtb2	Mm_Celera	2:103613661	AATGAATGTGTGCAT[A/G]AAGGACCAAGATGAA	99382
rs27374953	snp	A/C	0.426035	0.177515	intron-variant	Abtb2	Mm_Celera	2:103613548	AGTTAGCATGGCTAA[A/C]GTGAGGCTAGGGACC	99382
rs27374954	snp	A/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103613370	GCCATGAAAATGAAT[A/T]TATTGTCCATTCACT	99382
rs27374955	snp	C/T	0.391111	0.206368	intron-variant	Abtb2	GRCm38.p3	2:103613227	GGCAAATGGGAGGCC[C/T]CTTAAATGGAGACCT	99382
rs27374956	snp	A/G	0.132653	0.220748	intron-variant	Abtb2	Mm_Celera	2:103613212	CTTCATAGGACAGAA[A/G]GCAAATGGGAGGCCT	99382
rs27374957	snp	A/G	0.391111	0.206368	intron-variant	Abtb2	GRCm38.p3	2:103613205	TAGTTGTCTTCATAG[A/G]ACAGAAGGCAAATGG	99382
rs27374958	snp	A/G	0.336735	0.234472	intron-variant	Abtb2	Mm_Celera	2:103612981	ATTTTGTGGTATGGT[A/G]TGTTCTGGAGAAATT	99382
rs27374959	snp	G/T	0.391111	0.206368	intron-variant	Abtb2	Mm_Celera	2:103612664	GGGATCTCTATTAAT[G/T]TAAGCATTCGTGCAG	99382
rs27374960	snp	C/T	0.48	0.0979796	intron-variant	Abtb2	Mm_Celera	2:103612596	TCACTCAAGCATTCA[C/T]GAACCAGAATTTTGA	99382
rs27374961	snp	C/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103612387	TGACTTTGGTTCTTT[C/T]AGTCCTTCCTATTTT	99382
rs27374962	snp	G/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103612239	TGACCACCATGCATC[G/T]CTGTATCCAAGAAAC	99382
rs27374963	snp	A/C	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103612238	ATGACCACCATGCAT[A/C]GCTGTATCCAAGAAA	99382
rs27374964	snp	G/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103612127	GGATACCCTTGGAGA[G/T]CTTGGCTTGAACATC	99382
rs27374965	snp	C/T	0.489796	0.070696	intron-variant	Abtb2	Mm_Celera	2:103612107	GCCCTCCAAACAAGG[C/T]AATCGGATACCCTTG	99382
rs27374966	snp	C/T	0.426035	0.177515	intron-variant	Abtb2	Mm_Celera	2:103612042	TTTCCTAACAACTTC[C/T]TTCATTGTTGCCCAT	99382
rs27374967	snp	C/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103612029	AGCCTTCACTGGCTT[C/T]CCTAACAACTTCCTT	99382
rs27374968	snp	C/T	0.197531	0.244432	intron-variant	Abtb2	Mm_Celera	2:103612013	TGGCCTGCAAAGCTA[C/T]AGCCTTCACTGGCTT	99382
rs27374969	snp	C/T	0.396694	0.202437	intron-variant	Abtb2	Mm_Celera	2:103611998	CAAGATGGGCTGGAC[C/T]GGCCTGCAAAGCTAT	99382
rs27374970	snp	C/T	0.497778	0.0332592	intron-variant	Abtb2	Mm_Celera	2:103611971	TGGTAAGGTGGCCTG[C/T]CTCAGATGTAGCAAG	99382
rs27374971	snp	C/T	0.336735	0.234472	intron-variant	Abtb2	Mm_Celera	2:103611930	CATTCAGAATTCATT[C/T]GCTGGGTTAAAATGC	99382
rs27374972	snp	C/T	0.426035	0.177515	intron-variant	Abtb2	Mm_Celera	2:103611928	ATCATTCAGAATTCA[C/T]TCGCTGGGTTAAAAT	99382
rs27374973	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103611912	CATTTGCTTAAAAGG[C/T]ATCATTCAGAATTCA	99382
rs27374974	snp	A/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103611836	GATATGAGGGCTCTG[A/T]GTATAATTCTTGTCA	99382
rs27374975	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103611811	GATGAACAAGCTTCA[A/G]ATGTCCTTTGATATG	99382
rs27374976	snp	A/G	0.391111	0.206368	intron-variant	Abtb2	Mm_Celera	2:103611773	TATTTCAAGTTCAAG[A/G]GCAATGCAGAATGGG	99382
rs27374977	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103611521	ATTCCTGCCCTTCAC[C/T]CTGATTCCATCATGT	99382
rs27374978	snp	A/G	0.497778	0.0332592	intron-variant	Abtb2	Mm_Celera	2:103611502	GTGTTCCTCACCTTG[A/G]GATATTCCTGCCCTT	99382
rs27374979	snp	G/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103611431	GCCTGCATGCAGCAG[G/T]CTGTAAAATAGCTCC	99382
rs27374980	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103611249	AAATGTGAAGCGCCT[A/G]GTATGAGAACATTTC	99382
rs27374981	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103610944	AATTACACTTGGCAA[A/G]CCCAGGACAAAAATT	99382
rs27374982	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103610676	CTTAACAAGTTGCCC[C/T]AGCTTAGAACCTCTT	99382
rs27374983	snp	A/G	0.132653	0.220748	intron-variant	Abtb2	Mm_Celera	2:103610615	ACAATCATACAAGAG[A/G]CAGAACAAAGGAAGG	99382
rs27374984	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103610544	CAGTAAATTGCATGA[A/G]TGGATATTTCAAGTT	99382
rs27374985	snp	C/T	0.391111	0.206368	intron-variant	Abtb2	Mm_Celera	2:103610516	GTTAAGTATAGTCTC[C/T]CACTCCGTGTCCCAG	99382
rs27374986	snp	A/C	0.391111	0.206368	intron-variant	Abtb2	Mm_Celera	2:103610446	ACCCAGAAACACCAC[A/C]TGGGCATTTCTAGTC	99382
rs27374987	snp	C/T	0.132653	0.220748	intron-variant	Abtb2	Mm_Celera	2:103610442	GAAAACCCAGAAACA[C/T]CACCTGGGCATTTCT	99382
rs27374988	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103610421	ATACCAGCTTTGGAA[A/G]GGTTTGAAAACCCAG	99382
rs27374989	snp	A/G	0.391111	0.206368	intron-variant, downstream-variant-500B	Abtb2, LOC105244251	Mm_Celera	2:103610334	GGTCTGTAGAGGGGC[A/G]CACAGGCTGCTCTCT	99382
rs27374990	snp	C/T	0.32	0.24	intron-variant, downstream-variant-500B	Abtb2, LOC105244251	Mm_Celera	2:103610323	CAGGAAGAAGAGGTC[C/T]GTAGAGGGGCGCACA	99382
rs27374991	snp	C/T	0.32	0.24	intron-variant, downstream-variant-500B	Abtb2, LOC105244251	Mm_Celera	2:103610288	TGTCAAGGACGTGCC[C/T]TTTGAGCAGCACTGA	99382
rs27374992	snp	C/T	0.231111	0.249285	intron-variant, downstream-variant-500B	Abtb2, LOC105244251	Mm_Celera	2:103610259	AAACATAGTTTGTTC[C/T]TGCTCCCATTCTTTG	99382
rs27374993	snp	C/T	0.489796	0.070696	intron-variant, downstream-variant-500B	Abtb2, LOC105244251	Mm_Celera	2:103610177	TTTTGATGTTGATAC[C/T]GTCAAGTGACCACTT	99382
rs27374994	snp	G/T	0.124444	0.216185	intron-variant, downstream-variant-500B	Abtb2, LOC105244251	Mm_Celera	2:103610107	TGTTTATACGGCCTT[G/T]GTTAAGAAAGGCATC	99382
rs27374995	snp	A/T	0.124444	0.216185	intron-variant, downstream-variant-500B	Abtb2, LOC105244251	Mm_Celera	2:103610106	TTGTTTATACGGCCT[A/T]TGTTAAGAAAGGCAT	99382
rs27374996	snp	C/T	0.497778	0.0332592	intron-variant, downstream-variant-500B	Abtb2, LOC105244251	Mm_Celera	2:103610053	CTCTATAGAAACATA[C/T]GCTAGTAAATGCAAT	99382
rs27374997	snp	A/G	0.375	0.216506	intron-variant, downstream-variant-500B	Abtb2, LOC105244251	Mm_Celera	2:103609986	TGAACACACACACAC[A/G]TTATACCCACACATA	99382
rs27374998	snp	C/T	0.396694	0.202437	intron-variant, downstream-variant-500B	Abtb2, LOC105244251	Mm_Celera	2:103609883	AGGGAAAGAATAAAA[C/T]CCTGTCTCTATGTCA	99382
rs27374999	snp	C/T	0.391111	0.206368	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103609791	GTTTCCTAAAGAAAG[C/T]ATTCCTCGATGGATC	99382
rs27375000	snp	A/G	0.244898	0.249948	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103609738	TGAGCGAGCCTTCCC[A/G]TGCCAGAGTCCTTCA	99382
rs27375001	snp	C/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103609615	ATCACTCAAGGGCCC[C/G]AGGCTCAACAGCCAA	99382
rs27375002	snp	C/T	0.197531	0.244432	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103609563	ACAAGGACATCATGC[C/T]TTTTCTGCTGTTCTG	99382
rs27375003	snp	A/G	0.444444	0.157135	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103609551	TATCAGCTGGTCACA[A/G]GGACATCATGCCTTT	99382
rs27375004	snp	A/C	0.48	0.0979796	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103609550	GTATCAGCTGGTCAC[A/C]AGGACATCATGCCTT	99382
rs27375005	snp	C/G/T	0.489796	0.070696	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	GRCm38.p3	2:103609489	CACCAGAGTTTAATT[C/G/T]CCCACAAGAGTAAGG	99382
rs27375006	snp	G/T	0.391111	0.206368	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	GRCm38.p3	2:103609390	GATGCAGATATGGCT[G/T]CTATTTAGGACCAGA	99382
rs27375007	snp	C/T	0.391111	0.206368	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103609368	CCAGAGAGGTGCAAA[C/T]AAGTGAGATGCAGAT	99382
rs27375008	snp	G/T	0.473373	0.11227	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103609347	GCTGATCTTAACTCT[G/T]CCCTGCCAGAGAGGT	99382
rs27375009	snp	G/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103609271	AGGAATGTAGAAAAT[G/T]AAACACACCAGGAAC	99382
rs27375010	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103609245	GCCCTTTGGCTTCTG[C/T]TGGAGTTGACAGGAA	99382
rs27375011	snp	A/C	0.391111	0.206368	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103609206	AGGAGAGAAGAAATG[A/C]TAATGGTTCCAACTT	99382
rs27375012	snp	C/T	0.48	0.0979796	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103609168	CACCATGGCCATCTG[C/T]CTTAGTTCTATAAAT	99382
rs27375013	snp	C/T	0.231111	0.249285	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103609128	GCCTTCCTGTGACTC[C/T]CTGTCCTGACCAATG	99382
rs27375014	snp	C/T	0.391111	0.206368	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103609125	TGGGCCTTCCTGTGA[C/T]TCCCTGTCCTGACCA	99382
rs27375015	snp	A/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103609040	GAGCTCTGTGATGGG[A/G]TTGCCTAGACCAGCA	99382
rs27375016	snp	C/T	0.231111	0.249285	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103608980	GTGTAAAGTAGAACA[C/T]GCTTGACTGGTTAAT	99382
rs27375017	snp	A/G	0.48	0.0979796	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103608830	TAGAGCACACATTAG[A/G]GTTCACAGTTAAACA	99382
rs27375018	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103608545	TGCTAGCTGAAATCA[C/T]TGCACTGTGGCTCTC	99382
rs27375019	snp	A/T	0.489796	0.070696	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103608490	AAAGCAGAGCCACAT[A/T]CCCTCCCTACCATTT	99382
rs27375020	snp	A/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103608380	ACGTGACTCAAGTGC[A/G]AGGCCCGGTGTCAGC	99382
rs27375021	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103608379	GACGTGACTCAAGTG[C/T]GAGGCCCGGTGTCAG	99382
rs27375022	snp	A/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103608331	ACCGTATACTCTTCT[A/G]AACTGACACTGTTCC	99382
rs27375023	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103608264	AGTGCACCTGCAGGC[C/T]ACTCTTCCCCATCCT	99382
rs27375024	snp	A/T	0.444444	0.157135	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103608205	AGAGACCCAGCTTAG[A/T]GTGTTGGTTTCCTGC	99382
rs27375025	snp	C/T	0.32	0.24	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103608114	TCACCATGTGCACAC[C/T]CGGGAAGACACTGCC	99382
rs27375026	snp	A/G	0.391111	0.206368	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	GRCm38.p3	2:103608021	GGACCGTTTCCAACC[A/G]CAAGAGCTTCCTGTC	99382
rs27375027	snp	C/T	0.497778	0.0332592	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103607930	CTCGAATAACTGCTC[C/T]GTAGACTGGATTTTT	99382
rs27375028	snp	G/T	0.231111	0.249285	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103607781	TGGAGATAGAAATCA[G/T]CTTGATACGACAGAC	99382
rs27375029	snp	G/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103607731	AACGGTAAGGGGAAG[G/T]AGGAAAACCTCTCCG	99382
rs27375030	snp	A/G	0.444444	0.157135	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103607543	ACATGCCTGCAGCTT[A/G]AGGAGAATACATATG	99382
rs27375031	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103607505	GCTGTAAGGCAAGGT[C/T]GCCTTGTGCCTCAGG	99382
rs27375032	snp	A/G	0.444444	0.157135	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103607096	AGTCTTCATTTTCCT[A/G]AAGCAGAAATACATG	99382
rs27375033	snp	A/G	0.444444	0.157135	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103606856	TTCCTTTTCTCTTTT[A/G]GAAGCCCCCTCCTAT	99382
rs27375034	snp	C/T	0.231111	0.249285	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103606744	GAATTTCTTAGGACA[C/T]CAAATTCTGAGGACT	99382
rs27375035	snp	A/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103606708	AGAACAGTACACCCA[A/G]GAGACTCCATACATC	99382
rs27375036	snp	A/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103606683	CGGTGTAAGAGGGAG[A/G]GCTGACAATAGAACA	99382
rs27375037	snp	A/T	0.497778	0.0332592	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103606674	AATGACTCTCGGTGT[A/T]AGAGGGAGGGCTGAC	99382
rs27375038	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103606656	GAACAGTGGGTAATA[C/T]TGAATGACTCTCGGT	99382
rs27375039	snp	A/G	0.48	0.0979796	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103606630	TTCTGAGCCAGTGTC[A/G]TGTTGTCCATGAACA	99382
rs27375040	snp	A/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103606514	AAGGAGACAGAGATG[A/G]GAAAGGACTGGATAA	99382
rs27375041	snp	A/T	0.132653	0.220748	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103606216	GTAGAGCACAGTCTC[A/T]GTCTCCAAGGAAAAC	99382
rs27375042	snp	A/G	0.231111	0.249285	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103605725	TCTTTTGAGTAGTTG[A/G]TAAGTGTAAAATGAG	99382
rs27375043	snp	G/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103605436	ATGTGTCTCTGATAA[G/T]TCAAGGTCATAGTGT	99382
rs27375044	snp	A/T	0.231111	0.249285	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103605384	TTGAGGACAGAGGCT[A/T]TTGAAATGTAATGCA	99382
rs27375045	snp	A/G	0.32	0.24	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103605287	CCTGTACAAGACAGA[A/G]TTACCTGAAGTCTGA	99382
rs27375046	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103605261	GGTGTCTTCTGATGG[C/T]TTGGAAGGATCCTGT	99382
rs27375047	snp	A/C	0.231111	0.249285	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103605215	CTGCCTGTAGTTAGT[A/C]TTCCCCATATTCAGT	99382
rs27375048	snp	A/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103605172	GACTCATGGGTTCAA[A/G]TAGTTGTGATAGGAA	99382
rs27375049	snp	C/T	0.231111	0.249285	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103605060	GAGGGTTGATGACAT[C/T]GACTCTATTTGGAAG	99382
rs27375050	snp	A/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103604672	ACTTCTCTTTAGTCC[A/T]TTCTGTGATGCTGCT	99382
rs27375051	snp	A/G	0.132653	0.220748	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103604636	CAGATCCTTGCGATG[A/G]CACAGGACGCACCCA	99382
rs27375052	snp	A/G	0.32	0.24	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103604630	TGAATGCAGATCCTT[A/G]CGATGGCACAGGACG	99382
rs27375053	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103604605	GTTGTCTATGTGGGT[C/T]ACAAGGATTTGAATG	99382
rs27375054	snp	A/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103603968	CAAGTGCAAGAACAG[A/T]ACTCAAAGGTGCATC	99382
rs27375055	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103603747	CGGATTTGGAAGTTG[C/T]CTTGAGATCGGAAGA	99382
rs27375056	snp	A/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103603654	TAGGAAGAGACCTGC[A/G]TGGAGGCCGGTGAGT	99382
rs27375057	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103603488	GGAGAGAGGCTAGCC[C/T]TTGGAGAGAGAGAAT	99382
rs27375058	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103603437	TCACAGGATAAGAAC[C/T]AGAGGAAGCAAGAAG	99382
rs27375059	snp	A/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103603375	CAGGTCCCTGCAGCC[A/T]TTCTGGTGCCTGACA	99382
rs27375060	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103603304	AGCACTTGCAATGTG[C/T]CTTTCTGGGTTTGTA	99382
rs27375061	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103603225	GTCCTGGCCACTGGG[C/T]TGACCTAGGGAGTAA	99382
rs27375062	snp	A/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103603155	TCTTTTGGAGGAAAT[A/T]TGTTTGGATCAGTTT	99382
rs27375063	snp	A/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103603033	TGCTGTTCCTGAAGC[A/G]TGTTCCTCCTCAGTG	99382
rs27375064	snp	A/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103602916	GAAATGTGTAATAAT[A/T]ACCCTGGTGTAGAAT	99382
rs27375065	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103602608	TCCAGCCCAGATCTT[C/T]TACCACAAGCCTAGT	99382
rs27375066	snp	C/G	0.391111	0.206368	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103602267	TTGCTGCTAGATATC[C/G]TCAGATAACAGAGTA	99382
rs27375067	snp	A/C	0.132653	0.220748	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103602015	TCATGTCTCCATTTT[A/C]GTGTATATAGTTTCA	99382
rs27375068	snp	C/T	0.432133	0.171253	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	GRCm38.p3	2:103601513	GTGGCACCTCTCTTG[C/T]TCATATGGCCTGGCT	99382
rs27375069	snp	A/G	0.497778	0.0332592	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103601338	TATTCACCCTACCTC[A/G]GGTAATACCTAGTGC	99382
rs27375070	snp	A/G	0.132653	0.220748	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103600672	GATTACACACCCTAT[A/G]AGCTGGGTGTCTCCC	99382
rs27375071	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103600573	GCAAGGAGCGTAAGA[C/T]AATACGTGGCAGTCT	99382
rs27375072	snp	A/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103600558	CAGTCTTTGTATTTT[A/G]CAAGGAGCGTAAGAT	99382
rs27375073	snp	A/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103600084	CCTCCAAAGGCCTGT[A/G]TTCCCCTAGGTTTTC	99382
rs27375074	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103599980	CCCTCTCTGCTGAGG[C/T]TGAGGGAAAGCTGTG	99382
rs27375075	snp	A/G	0.408163	0.193609	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103599841	CCTGGAAAGCACAGA[A/G]GGTGGCAGCTTCCAT	99382
rs27375076	snp	C/T	0.497778	0.0332592	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103599794	TCGAGTTCTGCAGTA[C/T]GTCAGAAGCACTAGG	99382
rs27375077	snp	C/T	0.231111	0.249285	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103599570	CTGATCACTTGGTTC[C/T]GAAGTTAATTTCTGT	99382
rs27375078	snp	C/T	0.132653	0.220748	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103598737	TAGCATGGAAGGACA[C/T]GAACTATACCCAAAA	99382
rs27375079	snp	A/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103598664	ATTTGAGACCAGAGG[A/G]GCCCAAGTGTTTGCC	99382
rs27375080	snp	G/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103597987	TACCTAAAACTTAGT[G/T]TCATTTCCTGGCTCT	99382
rs27375081	snp	G/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103597888	CTGTACTTAATGAGT[G/T]ATTCACAACAGCAAA	99382
rs27375082	snp	C/T	0.231111	0.249285	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103597397	AGATCCATAGTTAAG[C/T]CCTGTGGTTCATGGC	99382
rs27375083	snp	A/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103597352	TGAGAGATGGGAGAG[A/G]AGGTAGGAGCCAAGA	99382
rs27375084	snp	A/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103597134	TCAGTGTCTCAGAAA[A/T]GATACTGTCAAGCTT	99382
rs27375085	snp	A/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103597076	ATTGGGGATTAGTGT[A/G]CTCCTGGTACCAGGC	99382
rs27375086	snp	A/G	0.231111	0.249285	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103596820	CCTATGATATTTCAA[A/G]CTGAGGACGATCCAG	99382
rs27375087	snp	A/G	0.32	0.24	intron-variant	Abtb2, LOC105244251	Mm_Celera	2:103596695	ATGGTGGTCCCTTGA[A/G]CTTCGGATCCTTCTT	99382
rs27375088	snp	C/T	0.391111	0.206368	intron-variant	Abtb2, LOC105244251	Mm_Celera	2:103596497	TGGAGAGCAGGAGCG[C/T]TGTATTCCCAGGGTT	99382
rs27375089	snp	C/T	0.32	0.24	intron-variant	Abtb2, LOC105244251	Mm_Celera	2:103596468	AGGGAGTCTGGGGAG[C/T]TTGCATTTGAGGCTG	99382
rs27375090	snp	G/T	0.231111	0.249285	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103596304	GAAGCATCTGGGAAG[G/T]CTTGGCTTCTGTGAA	99382
rs27375091	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103595814	CAGTCACTAGTAATA[C/T]AGTAACGTCACTTCA	99382
rs27375092	snp	C/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	GRCm38.p3	2:103595762	AGATAAACTGATACA[C/G]TCTCTGTGGAGGTTG	99382
rs27375093	snp	A/G	0.32	0.24	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103595077	GTCTGTGTTGCTTAA[A/G]CTATCCCAGCAAAAG	99382
rs27375094	snp	C/T	0.231111	0.249285	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103594842	GTCTGATCCTTTTTC[C/T]TGTCTTCTGTAAACA	99382
rs27375095	snp	A/G	0.231111	0.249285	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103594709	TCTCTGCATTGTCAC[A/G]GGATTACTGCTGTGG	99382
rs27375096	snp	C/T	0.231111	0.249285	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103594686	GATCTTTGGGTCCGT[C/T]GCTCACATCTCTGCA	99382
rs27375097	snp	A/G	0.231111	0.249285	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103594560	TCTTCTCAGTTCTTC[A/G]CAGTTCTGTTACTAA	99382
rs27375098	snp	A/G	0.132653	0.220748	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103594408	TAGATTTTAGAAGGA[A/G]TAAAGAGTTGGGTCT	99382
rs27375099	snp	C/T	0.231111	0.249285	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103593794	CTTGGGTTTAGCTTT[C/T]TTTCTGATTTGCTCA	99382
rs27375100	snp	C/T	0.231111	0.249285	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103593498	AGAGCAGGGGATCTT[C/T]TTGCATTGCTCTACC	99382
rs27375101	snp	G/T	0.231111	0.249285	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103593030	TTCATACCTTTAGAC[G/T]TGAGACAGGAGACTC	99382
rs27375102	snp	A/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103592877	CCAACCACAATGGGA[A/G]AAGCAAAAACCTAAT	99382
rs27375103	snp	A/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103592553	ATCTGTCTGGCTTCT[A/G]ACTCTCAGCACCGAC	99382
rs27375104	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103592419	AGATTTCATCACTCT[C/T]GAAACTGGAAGCCTG	99382
rs27375105	snp	G/T	0.497778	0.0332592	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103592323	AACCCCTGTTGCTCA[G/T]TCCCTCACCACAGTG	99382
rs27375106	snp	A/G	0.32	0.24	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103592309	CCTCCAGCTGCAGAA[A/G]CCCCTGTTGCTCATT	99382
rs27375107	snp	A/C	0.32	0.24	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103592265	GTCACCAGGGACAAG[A/C]TCGTCACATCCAGCC	99382
rs27375108	snp	C/T	0.432133	0.171253	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	GRCm38.p3	2:103592239	ACAGAGGCTTAAAGA[C/T]GAAATCTCCAGTCAC	99382
rs27375109	snp	C/T	0.32	0.24	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103591995	CAGATCCAGATAGAA[C/T]GACTGTTGAGCCAAC	99382
rs27375110	snp	C/G	0.444444	0.157135	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103591864	TGCGACCGTATTAGG[C/G]ACCATGTGTTTTCAG	99382
rs27375111	snp	A/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103591736	TCCAGCCTAAGTCCA[A/G]GTCATTGCTATCTTG	99382
rs27375112	snp	A/C/T	0.244898	0.249948	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	GRCm38.p3	2:103591170	CTGTGCTCCTATGGG[A/C/T]GTACATGCACATGGA	99382
rs27375113	snp	G/T	0.231111	0.249285	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103590978	GAGATGGAGCTGCTG[G/T]TTGAACTAGATAGAA	99382
rs27375114	snp	A/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103590936	GTGGGTCTGAGAATG[A/G]TAGGTGGGCTATGGA	99382
rs27375115	snp	A/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103590749	ACAACCTTGCCTTTG[A/T]GGAAGAACAAGGGCC	99382
rs27375116	snp	A/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103590554	GTGCACTTCTGTTCA[A/G]ATTTTATGTTtcagg	99382
rs27375117	snp	C/T	0.231111	0.249285	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103590457	TCAAGGTAGGTGAGG[C/T]GGTCTGGGAGGCCAG	99382
rs27375118	snp	C/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103589961	GACCAGCCCTAATAG[C/G]AGTAGAGTACCTTAT	99382
rs27375119	snp	A/G	0.432133	0.171253	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	GRCm38.p3	2:103589921	ATGATGACTCTAACT[A/G]TAGTTGGTTTAGAAG	99382
rs27375120	snp	A/G	0.497778	0.0332592	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103589754	GGTTTTCATCGCTGC[A/G]CCTCCTTAGTACCCC	99382
rs27375121	snp	A/G	0.32	0.24	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103589473	TCCACAAAGAAGCAC[A/G]TTTGCATCCTGTCAG	99382
rs27375122	snp	C/T	0.48	0.0979796	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103589313	TGGTCTTTCGGATTT[C/T]TCCTGAGCTATCTCT	99382
rs27375123	snp	C/T	0.32	0.24	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103589052	CCTGCGCTGAGTTCT[C/T]TAGCTTCAAATGGGG	99382
rs27375124	snp	C/T	0.497041	0.0383476	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103588903	AGTAGGGAGCCAGCA[C/T]GCCAAATTTCTCCAG	99382
rs27375125	snp	A/C	0.32	0.24	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103588888	TGTGGCCCGCCATCG[A/C]GTAGGGAGCCAGCAT	99382
rs27375126	snp	A/G	0.142012	0.225474	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103588852	TTTGCTGAGAAGGAG[A/G]TGCCCACTCGGCATC	99382
rs27375127	snp	A/T	0.231111	0.249285	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103588733	TTTCTTCCCAGGTAA[A/T]TAAGAGAGGTTAGGC	99382
rs27375128	snp	A/G	0.497778	0.0332592	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103588507	TGTCATATGTGACTC[A/G]TGTCAGAGTGTCCCT	99382
rs27375129	snp	A/G	0.32	0.24	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103588313	AATATGTCAAGGACG[A/G]TGTGAAGAGAGCAGT	99382
rs27375130	snp	A/T	0.142012	0.225474	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103588307	ACTGACAATATGTCA[A/T]GGACGATGTGAAGAG	99382
rs27375131	snp	A/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103588259	CTGAAGCTGGGATCT[A/G]TCCTTAGAACCTTCT	99382
rs27375132	snp	C/T	0.132653	0.220748	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103588227	TAAAGACAAATTCCC[C/T]GAGTCAGAGATGGAG	99382
rs27375133	snp	A/G	0.244898	0.249948	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103588186	AGAAGGCAGGACTAC[A/G]GGAGAGAGGGCATCC	99382
rs27375134	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103588140	AATCTGTGTGGTATG[C/T]ATGCCCTTTCCTGAC	99382
rs27375135	snp	G/T	0.231111	0.249285	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103588139	TAATCTGTGTGGTAT[G/T]TATGCCCTTTCCTGA	99382
rs27375136	snp	A/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103588116	GATGCATGTTCTACA[A/T]TAGGCCTTAATCTGT	99382
rs27375137	snp	A/G	0.260355	0.249785	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103588034	TCAAAGAGAAGAAAA[A/G]ACAGGATACCCAAGT	99382
rs27375138	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103587883	CCTGTTTCTCTAAAC[C/T]GAGAGTTGGTGTTAG	99382
rs27375139	snp	C/G	0.32	0.24	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103587804	AACCTGTGATTCAGA[C/G]TCGGTCTGTTTTCTC	99382
rs27375140	snp	A/G	0.260355	0.249785	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103587745	ATGCTTAAGTTGATA[A/G]AAGAGTGAGCAGTAA	99382
rs27375141	snp	A/G	0.231111	0.249285	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103587670	TCCACTACCATCTTG[A/G]ACATGCTTCAGGTTG	99382
rs27375142	snp	A/G	0.244898	0.249948	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103587664	CTATGTTCCACTACC[A/G]TCTTGAACATGCTTC	99382
rs27375143	snp	C/G	0.231111	0.249285	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103587559	AGCAGGTATCACTAG[C/G]TTAGGCAGAGCTGTG	99382
rs27375144	snp	A/G/T	0.142012	0.225474	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	GRCm38.p3	2:103587493	TACTGCATTGATTTG[A/G/T]GAAAATCTAACAGGA	99382
rs27375145	snp	G/T	0.32	0.24	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103587492	TTACTGCATTGATTT[G/T]GGAAAATCTAACAGG	99382
rs27375146	snp	C/T	0.32	0.24	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103587410	TCTGAACTTTTAGGG[C/T]TGAGACATTATTAAA	99382
rs27375147	snp	C/G	0.336735	0.234472	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103587374	ACCCACAGAGGTCTG[C/G]TTTTTGTTGCTATCA	99382
rs27375148	snp	A/G	0.32	0.24	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103587296	AATCAAACGGTAACA[A/G]CAAAAGGATCTTAGG	99382
rs27375149	snp	G/T	0.497778	0.0332592	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103587083	CATAGGTACATGTGT[G/T]CAACTTACCTAGGTC	99382
rs27375150	snp	C/T	0.231111	0.249285	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103587048	TTCCTGTATGTTGAA[C/T]TGAGACCAGTGAATT	99382
rs27375151	snp	A/G	0.391111	0.206368	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103586808	CTTTGCTCTACCCAT[A/G]GTTCCTTTTCCTTAA	99382
rs27375152	snp	A/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103586138	CAGAAAAGGGAAGAT[A/G]AGGGCCAAACACAGA	99382
rs27375153	snp	A/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103585936	GATTCAAAGGGTGAA[A/G]TTAAAAGTCAATGGC	99382
rs27375154	snp	G/T	0.32	0.24	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103585766	ATGGCTGACAAACAC[G/T]TTACTATTGAACTAT	99382
rs27375155	snp	C/T	0.32	0.24	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103585695	AATTCTGGGCAGGTT[C/T]CTCTGCTTTGTTTAT	99382
rs27375156	snp	C/T	0.497778	0.0332592	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103585651	AGGTCTGGGCTTTGC[C/T]AGTCCAGTTTAGGTC	99382
rs27375157	snp	A/G	0.124444	0.216185	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103585570	TTAGCCATTATGGTG[A/G]TAGAGTAGGCCCAGT	99382
rs27375158	snp	C/G	0.32	0.24	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103585291	ACAGGCCCGTTTTTA[C/G]TTGGTATGTGTCTCA	99382
rs27375159	snp	C/T	0.244898	0.249948	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103585116	AAAACTGGTTTGCTC[C/T]TTTTCAGTGAGTTGT	99382
rs27375160	snp	A/G	0.244898	0.249948	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103584997	ATTCCTGTCCTGTAA[A/G]AGAAATGTCAGAGTT	99382
rs27375161	snp	C/T	0.497778	0.0332592	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103584422	AGGAGCTTGGAGTGC[C/T]TTGGAAAAAAGAATA	99382
rs27375162	snp	A/G	0.497778	0.0332592	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103584289	GGAACCTCTAAGTGT[A/G]TATCAGTCTGGCAAA	99382
rs27375163	snp	A/G	0.336735	0.234472	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103584045	AAAGCACTGTGTTTC[A/G]CCATGGCATTTTCAC	99382
rs27375164	snp	A/T	0.32	0.24	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103583903	TTAACTGGCTATATT[A/T]ATTTTAAACCTCCAA	99382
rs27375165	snp	A/T	0.32	0.24	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103583849	ATCCATATGACTGGC[A/T]GATTGCTGGAACATT	99382
rs27375166	snp	C/T	0.32	0.24	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103583789	TGATTTGAGCCCATA[C/T]GTATCTTCCTCTTTC	99382
rs27375167	snp	C/T	0.244898	0.249948	intron-variant, nc-transcript-variant	Abtb2, LOC105244251	Mm_Celera	2:103583765	GAGGGAGAGAATATG[C/T]GTATGTGTTGATTTG	99382
rs27389568	snp	C/G	0.32	0.24	intron-variant, upstream-variant-2KB	Abtb2, LOC105244251	Mm_Celera	2:103583480	GGATATTGCATCACT[C/G]TGTTGTCACCGTTTG	99382
rs27389569	snp	A/G	0.401235	0.199068	intron-variant, upstream-variant-2KB	Abtb2, LOC105244251	GRCm38.p3	2:103583460	AAAGGAAGGACACAA[A/G]GCCAGGATATTGCAT	99382
rs27389570	snp	A/G	0.32	0.24	intron-variant, upstream-variant-2KB	Abtb2, LOC105244251	Mm_Celera	2:103583326	TATACAGGCGTCTTA[A/G]TCAAACTTATTACAA	99382
rs27389571	snp	C/T	0.142012	0.225474	intron-variant, upstream-variant-2KB	Abtb2, LOC105244251	Mm_Celera	2:103582185	TAAATGGAGTTGATA[C/T]TATTGCTGCTCCCTT	99382
rs27389572	snp	A/C	0.32	0.24	intron-variant, upstream-variant-2KB	Abtb2, LOC105244251	Mm_Celera	2:103582091	GTGACACATTCCCTC[A/C]ATGGAGGCCAGGGTA	99382
rs27389573	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103581711	AGCTCTACGAGACAA[C/T]ATGCCATTAGACTGC	99382
rs27389574	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103581366	GACTTGGCCGTTTCT[C/T]TCCTCTGGCTGCAGA	99382
rs27389575	snp	C/T	0.432133	0.171253	intron-variant	Abtb2	GRCm38.p3	2:103581353	GCCATTTGTTTAGGA[C/T]TTGGCCGTTTCTCTC	99382
rs27389576	snp	G/T	0.336735	0.234472	intron-variant	Abtb2	Mm_Celera	2:103581115	ATCTTTGGAAGCTTC[G/T]GGCTCCTTGAGCCCA	99382
rs27389577	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103580908	GCAGCAAGGCCCAGG[C/T]GCCCCTTATGCTTAG	99382
rs27389578	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103580579	CAGCAGACCATAGTG[C/T]CAACTCCCATGTCCA	99382
rs27389579	snp	C/G	0.391111	0.206368	intron-variant	Abtb2	Mm_Celera	2:103580417	ACTGGTAAAGCTTCT[C/G]TTAATTACATCTCTA	99382
rs27389580	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103580337	GAAGCCTGGAGTGCT[A/G]GGCTTACCTGGGAAG	99382
rs27389581	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103579970	TCCTCTGCTATTAAA[C/T]GGGGATATCACAGTT	99382
rs27389582	snp	G/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103579943	CTGCCTGACCATCTG[G/T]TGTCTCAATTTTCCT	99382
rs27389583	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103579849	AAAGAATGTTCATAG[A/G]ATACTGTGTATATCC	99382
rs27389584	snp	A/G	0.391111	0.206368	intron-variant	Abtb2	Mm_Celera	2:103579669	GTGATCAGCTCTACT[A/G]TTTTCAGTCATTAAC	99382
rs27389585	snp	C/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103579598	ATTTCTATTTAACAT[C/G]TTCAGTTGTTAGCCT	99382
rs27389586	snp	C/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103579554	CATAGCCCAACAAGA[C/G]TGGTCAGGACTTGGG	99382
rs27389587	snp	C/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103579496	TATACTTTCTCAATC[C/G]TGTAATAGATTGAAT	99382
rs27389588	snp	C/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103578463	GGGACCTGGTGGTTT[C/G]GTCTTCATCTCAGAG	99382
rs27389589	snp	A/C/G	0.489796	0.070696	intron-variant	Abtb2	GRCm38.p3	2:103578048	TAGGGGAGAAGCTAG[A/C/G]AAAAAATAAATACTC	99382
rs27389590	snp	C/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103577828	ACGCCATCTTTTTAA[C/G]ATTAGCATTTGCTGT	99382
rs27389591	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103577397	GCCTGTGCTCTTCCA[C/T]CAAGCTACACCCTAG	99382
rs27389592	snp	G/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103577275	GCAATAGAAACCTGA[G/T]TCCAGGGAGAGATGA	99382
rs27389593	snp	A/G	0.244898	0.249948	intron-variant	Abtb2	Mm_Celera	2:103577180	AGTTAATGATTTGAA[A/G]GTCTTTCTTTCTAAA	99382
rs27389594	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103576994	GGACTCCCTAGAGTT[C/T]AGTAGAGCCCTGACA	99382
rs27389595	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103576790	AAAAGGGTCTTACTC[C/T]TCTTTGTTGACTTCA	99382
rs27389596	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103576678	CCTGTACGTAATAAA[A/G]GTTGTGAGTGGTAAA	99382
rs27389597	snp	A/T	0.497778	0.0332592	intron-variant	Abtb2	Mm_Celera	2:103576646	CGACTTGATTAGTTC[A/T]CTGGGCTAAAGTGAT	99382
rs27389598	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103576631	GTTGAACTTGGCTTC[C/T]GACTTGATTAGTTCA	99382
rs27389599	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103576566	TGTGAAAGTAATACA[A/G]GACTTTTAAATGAGC	99382
rs27389600	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103576211	AGAGAAAGAAGGGAC[A/G]GTGTGGGAAAGACCT	99382
rs27389601	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103576187	GGACAACAGAGCCTC[A/G]ATCAAGAAAGAGAAA	99382
rs27389602	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103576160	ATGGAGCCTGTGAGC[C/T]AATGCAGACGTGGAC	99382
rs27389603	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103576078	ATAGATGAAAGTTTT[A/G]AAGCTTTACAAAGCT	99382
rs27389604	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103575666	ATGCATATGGTTAGC[A/G]GCAAAGAAGCTTGGC	99382
rs27389605	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103575661	ATAGCATGCATATGG[C/T]TAGCGGCAAAGAAGC	99382
rs27389606	snp	C/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103575639	TTTGTGATCTAAGAG[C/G]GACAGCATAGCATGC	99382
rs27389607	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103575539	TGAGAAATGCCCCAG[C/T]ACCCTCTGTGATCTA	99382
rs27389608	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103575496	AGTTGGAAGGGAAAT[A/G]ATGGAGAAACATAGC	99382
rs27389609	snp	A/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103575430	GCTTTGCCTGTTTTT[A/T]AAAACAACCAAAATG	99382
rs27389610	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103575282	TAGTAGACTGGACAT[A/G]CCTAGAAACTACTGT	99382
rs27389611	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103575225	CTCATCTGTGATGTG[A/G]GCACCTTGTTGATTG	99382
rs27389612	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103575205	GGCAGGTGATTCCTG[C/T]TTTGCTCATCTGTGA	99382
rs27389613	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103575111	GCAATCCCTGTTTAA[C/T]GCTCCAGACTCCGAG	99382
rs27389614	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103575101	GATAACAAGAGCAAT[C/T]CCTGTTTAACGCTCC	99382
rs27389615	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103575073	CCACTGAGTACTTGT[C/T]CACCTCTGTCAAGAT	99382
rs27389616	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103574954	CTAATAATTGGTTTC[C/T]GGAGGTAGGAAGAAG	99382
rs27389617	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103574873	GCTACTTGAGTTTCT[C/T]ATGTAGGGTGGAGCA	99382
rs27389618	snp	A/C	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103574718	GATTGGAAAACACAG[A/C]TCTGCAAGGTAGGAC	99382
rs27389619	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103574306	TATTAGTGAACCCAT[A/G]TCCTCAAGCAAATCA	99382
rs27389620	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103574225	GACAAACACTAATCA[A/G]CACAGCACTGTGCCA	99382
rs27389621	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103574201	CGGTATTTTGTATTC[A/G]GAGTATAGGACAAAC	99382
rs27389622	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103573901	AGAATCAACCAATCC[C/T]GTCTCCTTTCTTTCT	99382
rs27389623	snp	G/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103573803	GGAGCTTGGGATGCA[G/T]GGACATGCAAGGGAG	99382
rs27389624	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103573686	GGCTGCCCCAGAGGG[A/G]AGTCCTTTACCAAGT	99382
rs27389625	snp	A/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103573550	TTGTAAATGGCCTAC[A/T]ATGTCTAGGTATCTT	99382
rs27389626	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103573394	CTATTTTGCTCAAAT[C/T]CCAAGTCTGCAAAGA	99382
rs27389627	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103573393	CCTATTTTGCTCAAA[C/T]CCCAAGTCTGCAAAG	99382
rs27389628	snp	A/G	0.244898	0.249948	intron-variant	Abtb2	Mm_Celera	2:103573279	TAGTAATCTTGCTGC[A/G]TTCCCATCAACTTGC	99382
rs27389629	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103573206	TGGTGGAGTTTTATA[A/G]CAGATATCCAGCAGG	99382
rs27389630	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103572754	TTTACCCGACTTCCC[C/T]GCTCTGAGCTGGAAG	99382
rs27389631	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103572542	TTAACACCTGGGTAG[A/G]CTGAGCAAGGAGGGC	99382
rs27389632	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103572348	CACTTATTTACCATC[C/T]GAGACAAGTGTCAAC	99382
rs27389633	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103571801	GAGGAACAAGAAAAC[A/G]GAAACAAAGATTTAC	99382
rs27389634	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103571711	AATACGTACTCATCA[C/T]GGACGGCACCCCACT	99382
rs27389635	snp	C/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103571508	GTCACAGTGGCAAAT[C/G]TAAGAGTTTAAGGCC	99382
rs27389636	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103571292	TTGATTCAGAACAGC[C/T]TTTCTAGGTTCCTTC	99382
rs27389637	snp	A/C	0.336735	0.234472	intron-variant	Abtb2	Mm_Celera	2:103570926	TTAATGTCTTCCAAC[A/C]AGGAGCTTAAGAGCT	99382
rs27389638	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103570743	GGTTACAGTTTATAC[A/G]GCTGAAGACCGAATG	99382
rs27389639	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103570608	TGAAATGAATGTTTG[C/T]TAGAGAAGCAATGAA	99382
rs27389640	snp	G/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103570558	TGGTCTCACTAACCA[G/T]CGACTAGGCTGATTT	99382
rs27389641	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103570502	GTTGTCGTCCCCTTC[A/G]TAACTTCGATGCCCA	99382
rs27389642	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103570397	ACCTTTACCTCACAC[C/T]TTCAACAGGCAGGAA	99382
rs27389643	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103570343	AACCACTTGGAACTT[C/T]TTCACTGGATAGTGA	99382
rs27389644	snp	G/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103570334	TGCTTACAAAACCAC[G/T]TGGAACTTCTTCACT	99382
rs27389645	snp	A/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103570292	GTCAGAGATCGGTTC[A/T]TCTAAGTTCTCGCAA	99382
rs27389646	snp	C/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103570276	CTGCAAGTGCAAAGT[C/G]GTCAGAGATCGGTTC	99382
rs27389647	snp	A/G	0.42	0.183303	intron-variant	Abtb2	GRCm38.p3	2:103570203	AGAGCCCAGCATGCT[A/G]AATGCCTTTTTCTGA	99382
rs27389648	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103569959	TGTGGCTTCAGCACT[A/G]GGAACACCAGTTCCA	99382
rs27389649	snp	A/C	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103569822	TCATTTCTGGCACTA[A/C]CACAGGACATTCTTG	99382
rs27389650	snp	A/G	0.498615	0.0262793	intron-variant	Abtb2	GRCm38.p3	2:103568403	AAAACTAAGCACTGG[A/G]TAGCTGCACCCCAAC	99382
rs27389651	snp	C/T	0.432133	0.171253	intron-variant	Abtb2	GRCm38.p3	2:103568378	GGCAGCTGCACGGCG[C/T]GGAGTCTAGAAAACT	99382
rs27389652	snp	G/T	0.244898	0.249948	intron-variant	Abtb2	Mm_Celera	2:103567890	GCTGCCCTGCTACGG[G/T]TTTCCCTGTTAGTTG	99382
rs27389653	snp	C/T	0.408163	0.193609	synonymous-codon	Abtb2	Mm_Celera	2:103566780	GGACTTGACCTTGGA[C/T]TCCGGGTATGGGGCC	99382
rs27389654	snp	A/G	0.5	0	synonymous-codon	Abtb2	Mm_Celera	2:103566738	CCCCATGGCCGGGAC[A/G]TACAGCTCCACATTG	99382
rs27389655	snp	C/T	0.408163	0.193609	upstream-variant-2KB	Abtb2	Mm_Celera	2:103566245	CTGATGATTGGTGAA[C/T]CGCCCGGGTGTATTT	99382
rs27389656	snp	C/T	0.489796	0.070696	upstream-variant-2KB	Abtb2	Mm_Celera	2:103565443	CGAGGGGGAAGAAGA[C/T]CTGCGGACCCGCACA	99382
rs27393566	snp	A/G	0.124444	0.216185	downstream-variant-500B	Abtb2	Mm_Celera	2:103718750	CCGTCAGGCTGAGAT[A/G]AGGAAGGTCCTGAGG	99382
rs27393567	snp	A/G	0.231111	0.249285	downstream-variant-500B	Abtb2	Mm_Celera	2:103718737	GGCCCAGGCCCCTCC[A/G]TCAGGCTGAGATGAG	99382
rs27393568	snp	A/G	0.124444	0.216185	downstream-variant-500B	Abtb2	Mm_Celera	2:103718636	CCTGGGAAATGAGGC[A/G]CATGAAAATTTGATG	99382
rs27393569	snp	C/T	0.231111	0.249285	utr-variant-3-prime	Abtb2	Mm_Celera	2:103717994	AGGTTGGTTCTAGGT[C/T]GGGCCTAGCTCTAAT	99382
rs27393570	snp	A/G	0.444444	0.157135	utr-variant-3-prime	Abtb2	GRCm38.p3	2:103717992	AGAGGTTGGTTCTAG[A/G]TCGGGCCTAGCTCTA	99382
rs27393571	snp	C/G	0.124444	0.216185	utr-variant-3-prime	Abtb2	Mm_Celera	2:103717793	CCAAATCCTGTCCTC[C/G]AAGCTGTGCCTTTGA	99382
rs27393572	snp	A/T	0.124444	0.216185	utr-variant-3-prime	Abtb2	Mm_Celera	2:103717466	GGCTTTAGGGGTACT[A/T]CCTGCTCTTCCCCTA	99382
rs27393573	snp	A/G	0.484429	0.0868505	utr-variant-3-prime	Abtb2	GRCm38.p3	2:103717439	GACACCCCCAGTGGA[A/G]GGAGGCTTGTAGGCT	99382
rs27393574	snp	A/G	0.231111	0.249285	synonymous-codon	Abtb2	Mm_Celera	2:103717246	GCAGGATGCCTTCCG[A/G]CAGCTCATCTATGGC	99382
rs27393575	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103717145	CACGGGCCTCACTTC[C/T]CTCTCTACCTGCAGA	99382
rs27393576	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103717123	ATGGAGAAGGCTATA[A/G]GAAGGCCACGGGCCT	99382
rs27393577	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103717111	GCAGGTTTGGGGATG[A/G]AGAAGGCTATAGGAA	99382
rs27393578	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103716866	AGCCTTGTGCTGGGC[C/T]GTGTGTAGTCACTGC	99382
rs27393579	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103716800	CTGGAAGTGAATGCT[C/T]GATACTTTCTGCATT	99382
rs27393580	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103716556	GCTTGACAAGACTCA[C/T]AGCATCCCACTCTCC	99382
rs27393581	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103716535	TAAGTCGCCAGCCCA[C/T]AGCAAGCTTGACAAG	99382
rs27393582	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103716403	CCTCACATCCCACTC[A/G]GCTATCCTCAGTTCT	99382
rs27393583	snp	C/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103716176	CTGGGGACAGTCAGC[C/G]ACTCCCACCACACTC	99382
rs27393584	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103716000	CCTGGGACTTAAAAG[A/G]GGACGCTTTCATTTC	99382
rs27393585	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103715873	GAAATCTCAGCCCAC[A/G]CCCGTGCCTATCCTG	99382
rs27393586	snp	A/C	0.401235	0.199068	intron-variant	Abtb2	GRCm38.p3	2:103715797	GGCTGAGTCTGCTCG[A/C]CAGTGGTACATGGCC	99382
rs27393587	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103715762	TGCCTGTGGGGTTCA[A/G]CCCAGGAGCATCAGA	99382
rs27393588	snp	A/C	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103715642	CTCAGATCCATGTGG[A/C]GGGGCCTGTCATCCA	99382
rs27393589	snp	A/G	0.197531	0.244432	intron-variant	Abtb2	Mm_Celera	2:103715576	ACATCCTGCAGGTAA[A/G]GGCAGGGCATGTAGC	99382
rs27393590	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103714901	AGGCAGCAGAGCAAG[C/T]GCCTCCTCTCCTCAG	99382
rs27393591	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103714864	ACTCACTTCCTAAGC[A/G]CTCTAGGCACAGATC	99382
rs27393592	snp	G/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103714691	CTTGTTTACTCTTGC[G/T]CCTGCCAGCACCTTG	99382
rs27393593	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103714661	CTAACAGAGCCTGGC[C/T]GTGCCTGCTGGAGCC	99382
rs27393594	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103714604	CCTGCTGTCAGGTTT[C/T]CTCCTAGACCCTCTG	99382
rs27393595	snp	C/T	0.432133	0.171253	intron-variant	Abtb2	GRCm38.p3	2:103714501	CACAGGGACAGACTA[C/T]TGAGCCACTGTGTGA	99382
rs27393596	snp	A/C	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103714475	TGGTGGCTAAGGAGA[A/C]ACAGAGTACTCACAG	99382
rs27393597	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103714429	CACTGTCCCAACTGA[A/G]TGAGGGTATCCCAGG	99382
rs27393598	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103714222	ACTTAGCCAGATCTG[A/G]ACATCTACCTGCCTT	99382
rs27393599	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103714192	GCTACCCTCAGCTCC[C/T]ACCCAGGGTTAGCCA	99382
rs27393600	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103714003	GTGACTGTAGCTGTG[C/T]TCAGATGTAGGATGG	99382
rs27393601	snp	G/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103713828	ATTTGATTGATAAGA[G/T]CTTGGCGACGAGATG	99382
rs27393602	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103713629	ACCCTCGAGTCACTG[A/G]GCATGAGAGCAGCTC	99382
rs27393603	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103713563	GGGGTGCAGAGGGGA[A/G]GCATGCCAGTGTGTA	99382
rs27393604	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103713421	ACCAGACTGCAGACT[A/G]CAGACTGCGCACAGA	99382
rs27393605	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103713222	AGAGAGGACCAGAGC[A/G]TGAGACCTTCAGGAA	99382
rs27393606	snp	A/G	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103713109	GTACAGAGAGCCACC[A/G]TGGAACACTCCTGGG	99382
rs27393607	snp	A/C	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103713049	CCCTGTATAGAGTAA[A/C]GATCCCATGGGAGAC	99382
rs27393608	snp	C/G	0.244898	0.249948	intron-variant	Abtb2	Mm_Celera	2:103713043	GTCTGGCCCTGTATA[C/G]AGTAAAGATCCCATG	99382
rs27393609	snp	A/G	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103713032	TGCTAGGCCCTGTCT[A/G]GCCCTGTATAGAGTA	99382
rs27393610	snp	A/C	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103712895	GAGGAGGGTTGGAGT[A/C]TCAGCTGAGAGAGAT	99382
rs27393611	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103712846	GGGCTTTGCACAAGG[C/T]TCAGGCTGAGCAACA	99382
rs27393612	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103712790	AATGGCTGGGCTATT[A/G]GGCAACCATGGTGTA	99382
rs27393613	snp	A/G	0.244898	0.249948	intron-variant	Abtb2	Mm_Celera	2:103712602	TCAGTGACCACAAGA[A/G]AGCCACCCAGTCCTC	99382
rs27393614	snp	C/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103712554	TTATGCATCTGGTCA[C/G]TCTGTCCCTGAGGGC	99382
rs27393615	snp	C/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103712348	CACAGCAATGGATCT[C/G]AGGCCATGTTCAAAC	99382
rs27393616	snp	A/G	0.432133	0.171253	intron-variant	Abtb2	GRCm38.p3	2:103712227	GAGCTGGGCCCAGCA[A/G]CCCAGGATGATGTAA	99382
rs27393617	snp	A/G/T	0.456747	0.140554	intron-variant	Abtb2	GRCm38.p3	2:103712093	GAAGTTCTCAGGGCC[A/G/T]CCTCCTGCTGAGTTA	99382
rs27393618	snp	G/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103712005	GGGACCAAGAGGACC[G/T]TATAACTTCTGTCCC	99382
rs27393619	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103711951	TTCATCTACCTTAGA[A/G]GAAAGAGCTATATAA	99382
rs27393620	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103711886	TGATGTGAATTTTTC[C/T]AAGTTTCAGGAACTT	99382
rs27393621	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103711804	GAAGTTCCTGGCTGA[C/T]TTGCCTATCTGCCCA	99382
rs27393622	snp	C/T	0.244898	0.249948	intron-variant	Abtb2	Mm_Celera	2:103711785	ACATGAAGCCTGCAT[C/T]TCTGAAGTTCCTGGC	99382
rs27393623	snp	A/G	0.475309	0.108333	intron-variant	Abtb2	GRCm38.p3	2:103711768	GCAATCCCAGCATGG[A/G]TACATGAAGCCTGCA	99382
rs27393624	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103711744	TTAGAGGAACATGAT[A/G]TCCCAGAGGCAATCC	99382
rs27393625	snp	A/G	0.336735	0.234472	intron-variant	Abtb2	Mm_Celera	2:103711288	AGGGCTTGTTCCCAC[A/G]CTCTTCTTTCTCCCC	99382
rs27393626	snp	C/T	0.497778	0.0332592	intron-variant	Abtb2	Mm_Celera	2:103711269	GTGTGTATCCATGCC[C/T]GCTAGGGCTTGTTCC	99382
rs27393627	snp	A/C	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103711060	CACAGATGAAATGAC[A/C]GTCTGTTCTGGCCAA	99382
rs27393628	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103711011	GCCATGGCAGTCCAG[A/G]CTGGAGCCCAGCCAA	99382
rs27393629	snp	G/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103710924	AAATATACATGCACA[G/T]CCATCCCACACACAT	99382
rs27393630	snp	A/T	0.336735	0.234472	intron-variant	Abtb2	Mm_Celera	2:103710913	GATGGCCGTGTAAAT[A/T]TACATGCACATCCAT	99382
rs27393631	snp	C/T	0.32	0.24	synonymous-codon	Abtb2	Mm_Celera	2:103710836	GCAGCTCATGTTTGA[C/T]ATCCTCAAGACCAGC	99382
rs27393632	snp	A/G	0.32	0.24	synonymous-codon	Abtb2	Mm_Celera	2:103710791	CATCAAGGAAGAGGA[A/G]TACAACGAGGAGCTG	99382
rs27393633	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103710666	GACAGCTTCCCTTCT[C/T]TCTGGCCAGGTGTTC	99382
rs27393634	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103710625	AGAGCCCACCCTGAA[A/G]AGGCTGTACTTTCCT	99382
rs27393635	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103710535	AAGGCCTTCCTCCAT[A/G]TCATCTGATGAACAG	99382
rs27393636	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103710512	GCACTAGGCCCTTAG[C/T]TTGGCTGAAGGCCTT	99382
rs27393637	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103710440	GCGTACTTTCTGGGT[A/G]CATCTGGTCATCCCT	99382
rs27393638	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103710427	TCTTGAGTGCCCTGC[A/G]TACTTTCTGGGTACA	99382
rs27393639	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103710359	TGTGCACAGATACAC[C/T]AGGGAGCTGGATGCT	99382
rs27393640	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103709916	GAACAGGATGCTGTC[C/T]GCTAGAGCACAAGGC	99382
rs27393641	snp	A/G	0.231111	0.249285	synonymous-codon	Abtb2	Mm_Celera	2:103709439	CCGAACGAAGGCCCT[A/G]CAGGAAGCCATGTAC	99382
rs27393642	snp	C/T	0.244898	0.249948	synonymous-codon	Abtb2	Mm_Celera	2:103709397	GAGCCAGGGCAGCAG[C/T]GAGGGGCCTGTGAGG	99382
rs27393643	snp	C/T	0.231111	0.249285	synonymous-codon	Abtb2	Mm_Celera	2:103709337	AGCAGATGTGCTGTC[C/T]CTAGAAGAGATCCTG	99382
rs27393644	snp	A/G	0.231111	0.249285	synonymous-codon	Abtb2	Mm_Celera	2:103709292	CAGAAATGTCCTGAG[A/G]AAGCTCCTGACTCAG	99382
rs27393645	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103709232	CAGTTGGGCACTGTC[C/T]ACCCATCTTGGGGAT	99382
rs27393646	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103709225	TATAGCTCAGTTGGG[C/T]ACTGTCCACCCATCT	99382
rs27393647	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103709054	CAGAGAAGTAGAAGA[A/G]CCTGAGATCACACAG	99382
rs27393648	snp	C/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103709005	AGAGGGTGATCCTGG[C/T]ACCCTGTGTTAAGGT	99382
rs27393649	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103708906	CCCATCAATGCATAG[A/G]AGGAAAGCAGAAAGG	99382
rs27393650	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103708789	GCAAGACTCCAGCGC[A/G]CAGTTCAGGGCTGTC	99382
rs27393651	snp	A/G	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103708728	GGGAACAAGAGAAGC[A/G]GTTACTAGAGAGCAG	99382
rs27393652	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103708725	GAGGGGAACAAGAGA[A/G]GCAGTTACTAGAGAG	99382
rs27393653	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103708702	GGCTGTGCTAGAGGT[A/G]GAACGTGGAGGGGAA	99382
rs27393654	snp	A/C/T	0.244898	0.249948	intron-variant	Abtb2	Mm_Celera	2:103708690	CCAGAGTCGTTAGGC[A/C/T]GTGCTAGAGGTGGAA	99382
rs27393655	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103708568	TGCTCCCAGAGTATC[C/T]CCAGGGCTTCACTCA	99382
rs27393656	snp	A/C	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103708524	TCCAGTCCTCTGTGA[A/C]GTTGGTGGTGATTTT	99382
rs27393657	snp	A/G	0.391111	0.206368	intron-variant	Abtb2	Mm_Celera	2:103708423	ACTGGATGAGCTCTG[A/G]CTTCTGACACGCTGG	99382
rs27393658	snp	C/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103708374	GTAGGTTCTTGGTCA[C/G]CATGGAGGCCCAAGA	99382
rs27393659	snp	C/T	0.231111	0.249285	synonymous-codon	Abtb2	Mm_Celera	2:103708198	CTGCTTCAGCCACTC[C/T]GCTGCCCACGGCCAC	99382
rs27393660	snp	A/G	0.244898	0.249948	synonymous-codon	Abtb2	Mm_Celera	2:103708105	GCTGGTCAGCTTGCT[A/G]CTGAGCCGGGGTGCT	99382
rs27393661	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103707945	TCCCATTTATACCCA[C/T]GTTATCATTGCCTGA	99382
rs27393662	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103707887	ATGAGCCTTCCCCTC[C/T]TGAGGACCTAGACAG	99382
rs27393663	snp	C/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103707867	AGAGAGGGCCCTGTA[C/G]GGTAATGAGCCTTCC	99382
rs27393664	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103707767	AGCTATGTGCTAACT[C/T]TAGAAACCCTTAAGG	99382
rs27393665	snp	A/G	0.124444	0.216185	synonymous-codon	Abtb2	Mm_Celera	2:103707606	CGGTGCCCATGTGGA[A/G]GGCTCAGCTGTGAAC	99382
rs27393666	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103707566	GTATGTCTTCTTCCT[A/G]TGCCTGACAGCTGCT	99382
rs27393667	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103707321	AAGCTGATTGGTGGG[A/G]AAGTATTGAGAAGAG	99382
rs27393668	snp	A/C	0.391111	0.206368	intron-variant	Abtb2	Mm_Celera	2:103707294	CTGTGTGAGTTCTCC[A/C]GAAGGTCTCTGAAGC	99382
rs27393669	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103706986	AGCCATTCCAGTCAG[C/T]GGCCAGCACCGTAGC	99382
rs27393670	snp	C/T	0.444444	0.157135	intron-variant	Abtb2	Mm_Celera	2:103706901	TGTTGGGCACCATAT[C/T]GTTTAATCTCAGTAA	99382
rs27393671	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103706889	AGTCCCTCAGTGTGT[C/T]GGGCACCATATTGTT	99382
rs27393672	snp	C/G	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103706881	CAGTGAGGAGTCCCT[C/G]AGTGTGTTGGGCACC	99382
rs27393673	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103706696	TCTTCAGAAGCCTGG[A/G]AGTGTGCAAAGCAAG	99382
rs27393674	snp	C/T	0.391111	0.206368	intron-variant	Abtb2	Mm_Celera	2:103706569	CTGACTGACAAGTCG[C/T]CAGCAGATACAGGCT	99382
rs27393675	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103706199	AAGAGGCACCAGTGA[C/T]ATGGCACTCAGTTGA	99382
rs27393676	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103706123	CCCACCTTGGGTTGG[A/G]CTGCTATGGCTGGCA	99382
rs27393677	snp	A/G/T	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103705912	AGGCCTAGCCAGGGC[A/G/T]CTCTCCGGGTGAGTT	99382
rs27393678	snp	C/T	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103705905	GAGAGCCAGGCCTAG[C/T]CAGGGCGCTCTCCGG	99382
rs27393679	snp	C/T	0.432133	0.171253	synonymous-codon	Abtb2	GRCm38.p3	2:103705669	TCCGTCCGTCCACCC[C/T]GACAGCAGGCATTGG	99382
rs27393680	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103705581	GTACCTGTGTCATCT[A/G]CTCTGGAAAGTCACC	99382
rs27393681	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103705210	ATCTCCAGCAGCCAG[A/G]CTGGGCGTGGTATTT	99382
rs27393682	snp	A/G	0.498615	0.0262793	intron-variant	Abtb2	GRCm38.p3	2:103705026	TGTTCCATGCCTGAC[A/G]ATTTAGCATCTACCT	99382
rs27393683	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103704730	ACCTCTCACTTGGGG[C/T]TGTAAGCTTATCATG	99382
rs27393684	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103704530	TCAACAACTCAGACC[A/G]GGGTTCCAGCCTAGG	99382
rs27393685	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103704155	TTGCTCTATGAACGC[C/T]GGTATTTAGAAACAG	99382
rs27393686	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103703955	GGGACAGCATAAAAA[C/T]GTGGCTTCCTTTCTC	99382
rs27393687	snp	C/G	0.132653	0.220748	intron-variant	Abtb2	Mm_Celera	2:103703716	GAAGGCTTTAGTCTA[C/G]CACATCACAGCTGAG	99382
rs27393688	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103703656	GGTGTTCGCTTCCTC[A/G]GGGCCTGCAGTGTTG	99382
rs27393689	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103703589	CCTCAGGCTGGTGTC[A/G]GTCGCATGCAGGCAC	99382
rs27393690	snp	C/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103703559	CAGAGCGAGGAGTGT[C/G]TGCACAGTGGAGAAC	99382
rs27393691	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103703428	TGAAGCGTGAGGCCA[A/G]GAGTGCTTTGTGGGG	99382
rs27393692	snp	A/G	0.475309	0.108333	intron-variant	Abtb2	Mm_Celera	2:103703240	TCAGAAGACTGCAGC[A/G]CACACCCGCTGTGGA	99382
rs27393693	snp	C/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103702827	TAAGCCTATCGACCA[C/G]CTAAGGCCAAGTGCA	99382
rs27393694	snp	G/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103702822	GCACCTAAGCCTATC[G/T]ACCACCTAAGGCCAA	99382
rs27393695	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103702792	TGACACTGGTAAAGC[A/G]AGAGTAAGAAGCAAG	99382
rs27393696	snp	A/G	0.498615	0.0262793	intron-variant	Abtb2	GRCm38.p3	2:103702750	GTGCCAGCCACTCAC[A/G]AGCTCCAGAGAAACC	99382
rs27393697	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103702727	CACTGGCATGTGAAC[A/G]GGACTGTGTGCCAGC	99382
rs27393698	snp	A/C	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103702579	GGTCCCCCAAACCTC[A/C]TGGACAACTATGGTA	99382
rs27393699	snp	C/T	0.432133	0.171253	intron-variant	Abtb2	GRCm38.p3	2:103702536	CAGTCAGCTCTGGGC[C/T]TCAAGATCCTGACAG	99382
rs27393700	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103702232	ACAGTCACACTCACA[C/T]ACCTCTTGGTCTCTC	99382
rs27393701	snp	A/G	0.465374	0.126941	intron-variant	Abtb2	GRCm38.p3	2:103702163	CAAGACCAGAGCAAG[A/G]CCAGCCATAGCTGAC	99382
rs27393702	snp	C/T	0.495	0.0497494	intron-variant	Abtb2	GRCm38.p3	2:103701934	AGTCCACTGCATTAG[C/T]CCATGTGTAGGAGGC	99382
rs27393703	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103701740	CCTGAAGAGACAAAG[A/G]GAAAATCTAGGCATT	99382
rs27393704	snp	A/C	0.455	0.143091	intron-variant	Abtb2	GRCm38.p3	2:103701500	GGCCTGGCCTGAGGG[A/C]TGCTTGAATTTCTGT	99382
rs27393705	snp	A/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103701454	TGCAGAAGCTGTTCA[A/T]GGGCCTGCTCCTGCT	99382
rs27393706	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103701385	TGCAGAGGTGCCTAA[A/G]TTTAAGATCATCATG	99382
rs27393707	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103701381	TGTCTGCAGAGGTGC[C/T]TAAATTTAAGATCAT	99382
rs27393708	snp	C/T	0.432133	0.171253	intron-variant	Abtb2	GRCm38.p3	2:103701054	GGCACCTGAGTTACA[C/T]TAAGTATCGTTCAAA	99382
rs27393709	snp	A/C	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103700975	TCTCTGTCCCATCAC[A/C]TATAACACCTCTCTG	99382
rs27393710	snp	C/T	0.487535	0.077957	synonymous-codon	Abtb2	GRCm38.p3	2:103700906	GCCAGGCCTGGACTG[C/T]GAGCCCCGGCAACTC	99382
rs27393711	snp	A/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103700656	TGGCACTGTCCTTTC[A/T]TGGATAAAGCAGCGC	99382
rs27393712	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103699440	CAAAACCTTCTCTTG[A/G]GCTAAGGGCTAAGGA	99382
rs27393713	snp	G/T	0.244898	0.249948	intron-variant	Abtb2	Mm_Celera	2:103699349	CACACACACACACGG[G/T]TTAATGGCCACACTC	99382
rs27393714	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103698874	TACAAGCATGCTCTA[C/T]GAAGAGAGAAGAACT	99382
rs27393715	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103698781	AGAACTGAGACTAGG[A/G]TCATGAATCTCTCTG	99382
rs27393716	snp	G/T	0.455	0.143091	intron-variant	Abtb2	GRCm38.p3	2:103698522	AGACACCACCTGAGA[G/T]ACAGAGGGATAATTC	99382
rs27393717	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103698243	GCCCTTCCAATAGGA[A/G]GCTGCAGCACAGGGA	99382
rs27393718	snp	G/T	0.197531	0.244432	intron-variant	Abtb2	Mm_Celera	2:103698037	GTCTCAGCAGGCAGA[G/T]AGATGGCTGCGCAGA	99382
rs27393719	snp	C/T	0.5	0	intron-variant	Abtb2	GRCm38.p3	2:103697077	AGTGTCATCCTTACA[C/T]ACTATGCTAGCTGTC	99382
rs27393720	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103697058	CAGAGTTCCAGCCCC[A/G]GGCAGTGTCATCCTT	99382
rs27393721	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103696981	CTCAGGATCCTGATC[A/G]ATGGGTGGATGTGAA	99382
rs27393722	snp	C/T	0.132653	0.220748	intron-variant	Abtb2	Mm_Celera	2:103696974	CCAGGTCCTCAGGAT[C/T]CTGATCGATGGGTGG	99382
rs27393723	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103696495	CCCTATCAACAGATA[C/T]TAAAGCAGTAAGAAT	99382
rs27393724	snp	A/G	0.432133	0.171253	intron-variant	Abtb2	GRCm38.p3	2:103696429	ACCTGTAAGAAGGCT[A/G]GAGCTGAGGCAGCCA	99382
rs27393725	snp	C/T	0.336735	0.234472	intron-variant	Abtb2	Mm_Celera	2:103696199	TAGTGACCCACAACC[C/T]TCTATGACTATGTTT	99382
rs27393726	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103695895	AGCTAGAAATTAGAG[A/G]TGTTTCCTGTTCCAT	99382
rs27393727	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103695879	AACAGAGCCTGCTTT[A/G]AGCTAGAAATTAGAG	99382
rs27393728	snp	A/C	0.32	0.24	intron-variant	Abtb2	GRCm38.p3	2:103695786	CCCAGGGTTTGGACT[A/C]CATAGCCTATAGGTA	99382
rs27393729	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103695658	TGCCCGCTCTCATAG[C/T]CTTGGTCAGTAGGCA	99382
rs27393730	snp	C/G	0.244898	0.249948	intron-variant	Abtb2	Mm_Celera	2:103695623	AAAACCCTGGCCCAG[C/G]CTTCCCACAGTGAAG	99382
rs27393731	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103695592	TGAGTTGCCATGACC[C/T]TATACCCAGGCAAGC	99382
rs27393732	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103695472	CTCCTCCTTTCTTAA[A/G]CTTCAAATGCTCTCA	99382
rs27393733	snp	A/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103695250	AATCTGGCAATCTTC[A/G]CAACATTTCTCTCCT	99382
rs27393734	snp	G/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103695214	GAAGTTTCTGTCTGT[G/T]GAATCTTCACTTGGT	99382
rs27393735	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103695181	TGGCATTTCAGAGCC[A/G]ACTCCAACTCTTCCA	99382
rs27393736	snp	A/G	0.244898	0.249948	intron-variant	Abtb2	Mm_Celera	2:103695081	AGTAAGACAATATTG[A/G]CTTTATTCTACATGG	99382
rs27393737	snp	A/G	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103695021	AGTCCAAGATGTGAG[A/G]CAAACTAGAATCCCT	99382
rs27393738	snp	A/C	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103694772	AATCTGTACCAGATG[A/C]GTTTTAATAAGAAAC	99382
rs27393739	snp	A/G	0.432133	0.171253	intron-variant	Abtb2	GRCm38.p3	2:103694735	TGTGTAGCATATCTG[A/G]CAAGCGGTTTCTAGT	99382
rs27393740	snp	G/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103694356	AGTCTGGTAAGGCAA[G/T]CCACCCCAATCCTGG	99382
rs27393741	snp	G/T	0.336735	0.234472	intron-variant	Abtb2	Mm_Celera	2:103694262	CTAGAGCCACCACCA[G/T]CAAGAGGCCGGAGAA	99382
rs27393742	snp	C/T	0.444444	0.157135	intron-variant	Abtb2	Mm_Celera	2:103694260	CTCTAGAGCCACCAC[C/T]AGCAAGAGGCCGGAG	99382
rs27393743	snp	C/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103694199	TCATGTCCCAATTGT[C/G]ATACAGTTGACTGCA	99382
rs27393744	snp	G/T	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103694061	GTGCTCTGCTTGTCC[G/T]TGTGTAGAGTACACA	99382
rs27393745	snp	A/G	0.132653	0.220748	intron-variant	Abtb2	Mm_Celera	2:103693618	AAGTCAGCCAGACAT[A/G]GTGACACACAACGTT	99382
rs27393746	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103693224	TACAGATGCCCCTCT[C/T]ATTGTGAGATGGGTC	99382
rs27393747	snp	C/T	0.391111	0.206368	intron-variant	Abtb2	Mm_Celera	2:103693113	TCAAGTGCCCTAACA[C/T]TGTGAGGATGAAGTG	99382
rs27393748	snp	C/T	0.497778	0.0332592	intron-variant	Abtb2	Mm_Celera	2:103693075	ATCAGGCAGAGGGAC[C/T]GCTGTGGACAAAGAT	99382
rs27393749	snp	C/T	0.497778	0.0332592	intron-variant	Abtb2	Mm_Celera	2:103692965	TACAAACCTGGTAAG[C/T]CCTGTATGTCATAGG	99382
rs27393750	snp	C/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103692856	ATGGCTCCTAATGGA[C/G]TTTCTTTGCTGAAAG	99382
rs27393751	snp	C/T	0.124444	0.216185	intron-variant	Abtb2	Mm_Celera	2:103692846	AACTCAGTAGATGGC[C/T]CCTAATGGACTTTCT	99382
rs27393752	snp	A/G	0.497778	0.0332592	intron-variant	Abtb2	Mm_Celera	2:103692773	GTGCAGCTCAGGAGT[A/G]AATGGACCCCTGAGA	99382
rs27393753	snp	C/G	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103692624	TTAGCCCCAGTCTGC[C/G]TGGTTCTAGGAAGTC	99382
rs27393754	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103692598	TTTCCAGCTACTTTC[C/T]TAGAGCTACCTTAGC	99382
rs27393755	snp	C/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103692568	CTGCCTCTCCCTTTC[C/G]TGCCTTATCCTAGTT	99382
rs27393756	snp	A/C	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103692501	TCGAGGCCGGTTGTG[A/C]TCTTTCCATCATGAC	99382
rs27393757	snp	A/G	0.46875	0.121031	intron-variant	Abtb2	GRCm38.p3	2:103692402	AAGGCCCTTCCTGCT[A/G]CGTGGAAAAGGGTGT	99382
rs27393758	snp	A/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103692269	GGTTTGCTGTCACAC[A/T]CCTGCCACCCCATGT	99382
rs27393759	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103692186	GGCACATGGCAGCAC[C/T]GGGCCCTGTGGATGA	99382
rs27393760	snp	A/G	0.497778	0.0332592	intron-variant	Abtb2	Mm_Celera	2:103692148	GCTGTGTCAGCGAGT[A/G]TGGAAAGAGAAAGTG	99382
rs27393761	snp	C/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103692124	GAGAGAATGTATGGT[C/T]CGTAGTCAGCTGTGT	99382
rs27393762	snp	G/T	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103692086	TAGGTTGGAAGTCCT[G/T]GCCTGTCTGGCTTTT	99382
rs27393763	snp	C/G	0.391111	0.206368	intron-variant	Abtb2	Mm_Celera	2:103691984	TTGTCTTGGGAACAA[C/G]TGAGCCCTGGGATCC	99382
rs27393764	snp	A/G	0.444444	0.157135	intron-variant	Abtb2	Mm_Celera	2:103691813	ACTTTCGAGTGTGTC[A/G]CCTTTCTTCCCTAGA	99382
rs27393765	snp	C/T	0.231111	0.249285	intron-variant	Abtb2	Mm_Celera	2:103691794	TAGAAGCTCCATATG[C/T]GACACTTTCGAGTGT	99382
rs27393766	snp	A/G	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103691291	CTCTATTGGCCAGCA[A/G]ATTCAATGTGCCCTA	99382
rs27393767	snp	C/T	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103691273	CCATTACACCTCCTA[C/T]TTCTCTATTGGCCAG	99382
rs27409668	snp	A/C	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103691169	GCACTCTTTGAGACG[A/C]TGGTGTCCAGCTTTC	99382
rs27409669	snp	C/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103691146	ATGGGGTTTTTAATA[C/T]TTTGAGTGCACTCTT	99382
rs27409670	snp	A/G	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103690963	GCAGCTAGGAGCTTT[A/G]GCAGATCAAGAGCCA	99382
rs27409671	snp	C/T	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103690945	CAGACCCTGACAGTG[C/T]GAGCAGCTAGGAGCT	99382
rs27409672	snp	A/G	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103690909	TTTTGAGGTGCTTCC[A/G]AGGCCCTTCTGGAGA	99382
rs27409673	snp	A/G	0.497041	0.0383476	intron-variant	Abtb2	Mm_Celera	2:103690862	GAGAGTGCCTGGTAT[A/G]GGGAAGGCCTCCCTC	99382
rs27409674	snp	C/G	0.497041	0.0383476	intron-variant	Abtb2	GRCm38.p3	2:103690698	CCCTGCGGGCTGCCC[C/G]TTGCCTGGGACTTCC	99382
rs27409675	snp	A/G	0.35503	0.226867	intron-variant	Abtb2	Mm_Celera	2:103690394	ATTCTGATTATAACA[A/G]ACCAGGGACTTCTTA	99382
rs27409676	snp	A/C	0.165289	0.235211	intron-variant	Abtb2	Mm_Celera	2:103690363	AGAAAGAGGCAAAGT[A/C]GAGTTCAGGCCGGGA	99382
rs27409677	snp	A/G	0.444444	0.157135	intron-variant	Abtb2	Mm_Celera	2:103690359	AGAAAGAAAGAGGCA[A/G]AGTAGAGTTCAGGCC	99382
rs27409678	snp	A/G	0.415225	0.187619	intron-variant	Abtb2	GRCm38.p3	2:103690277	CTTGTTCCCATTTAC[A/G]GCAGACTGTAGGTCT	99382
rs27409679	snp	A/G	0.497041	0.0383476	intron-variant	Abtb2	Mm_Celera	2:103690178	GTGTAGACCCTCAAC[A/G]TTAAGATCAAGCCTG	99382
rs27409680	snp	A/G	0.375	0.216506	intron-variant	Abtb2	GRCm38.p3	2:103690091	AGGGGAGGGGAGTCA[A/G]TAGTCACTTCTGATG	99382
rs27409681	snp	C/T	0.426035	0.177515	intron-variant	Abtb2	Mm_Celera	2:103689983	ATGCATACCTAGGAG[C/T]AATATGATCTGACTT	99382
rs27409682	snp	A/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103689513	TGGTAATTGCTAATG[A/T]ACTGTGCAGATGTTA	99382
rs27409683	snp	C/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103689110	GATCACACTGAGGGC[C/T]GTCTCTCCCATCCAA	99382
rs27409684	snp	A/G	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103688772	TCAGAGGCACCCACC[A/G]GTTGGTGTTCGTTGA	99382
rs27409685	snp	C/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103688596	TTTCTTCCTCTGATT[C/T]CCAGAGACTGTTCCT	99382
rs27409686	snp	A/G	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103688573	TGTTCTAAGAGTCCA[A/G]TTCAGCGTTTCTTCC	99382
rs27409687	snp	A/G	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103688533	GGTTAGTAGTTTGCC[A/G]TTGGTGAGCATATCC	99382
rs27409688	snp	G/T	0.475309	0.108333	intron-variant	Abtb2	GRCm38.p3	2:103688489	CATTACCAGTTCCTA[G/T]TTAGCAAATGTTTCA	99382
rs27409689	snp	G/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103688390	ACAGGGCTTCTGGTA[G/T]TCCCAGATGCAAATA	99382
rs27409690	snp	A/T	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103688282	GACTAGAATTGTTGA[A/T]AGACCCTGGCAGATC	99382
rs27409691	snp	C/T	0.46875	0.121031	intron-variant	Abtb2	GRCm38.p3	2:103687719	AGGGAGAAAGAGTGG[C/T]AGTTACAATGGCTAC	99382
rs27409692	snp	A/G	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103687557	TGCATGGGAGGCAAG[A/G]GACCTGTTCTCTTGC	99382
rs27409693	snp	C/T	0.456747	0.140554	intron-variant	Abtb2	GRCm38.p3	2:103686983	TATTTTTCAGAAGGG[C/T]GGTGTATCAGGCCTG	99382
rs27409694	snp	A/G	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103686588	ATACTGTTCAGTGGG[A/G]CCTCAGTATCTCTCT	99382
rs27409695	snp	A/G	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103686569	GACATTCCCTACTAA[A/G]CCTATACTGTTCAGT	99382
rs27409696	snp	G/T	0.456747	0.140554	intron-variant	Abtb2	GRCm38.p3	2:103686532	ACATGCTAGCATCCC[G/T]TTTGTGTGGAGCACA	99382
rs27409697	snp	A/G	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103686413	GGACTCATTTTGGCG[A/G]CGTGGCTATTCAAGT	99382
rs27409698	snp	G/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103686296	GAGACTGTGATTCCA[G/T]GTGTGGCAGTGAAGG	99382
rs27409699	snp	C/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103686139	AAATAGCTGAGAAAA[C/T]TTGCCTCCTTGCAGT	99382
rs27409700	snp	A/G	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103685912	ACCACTGTGGGAGCA[A/G]TGAAATCCAAAATTT	99382
rs27409701	snp	C/G	0.375	0.216506	intron-variant	Abtb2	Mm_Celera	2:103685906	GGAACCACCACTGTG[C/G]GAGCAATGAAATCCA	99382
rs27409702	snp	A/G	0.492188	0.0620098	intron-variant	Abtb2	GRCm38.p3	2:103685449	GGCTAGGCAGACTGC[A/G]TTAGAGAGAGGAGAG	99382
rs27409703	snp	G/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103685409	TGTGGAGAAAGTGTT[G/T]CGGTTGCAAAAGTTG	99382
rs27409704	snp	A/G	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103685346	TCAAGCCCATACAGT[A/G]GGAGGCGTGGCCAGA	99382
rs27409705	snp	A/G	0.48	0.0979796	intron-variant	Abtb2	GRCm38.p3	2:103685319	CAGCTGGAACCCAAG[A/G]CATTCTGAAAGTCAA	99382
rs27409706	snp	A/G/T	0.459184	0.136902	intron-variant	Abtb2	GRCm38.p3	2:103685156	GAAGAAACATAAAAC[A/G/T]ACAGTGGCCTGGCAC	99382
rs27409707	snp	C/T	0.473373	0.11227	intron-variant	Abtb2	GRCm38.p3	2:103684510	TATACATATTGGTGC[C/T]GCATGTACTTACCCT	99382
rs27409708	snp	C/G	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103684197	AAGGCTTTGAAAGCA[C/G]CAGGCATCCATGTAG	99382
rs27409709	snp	A/G	0.426035	0.177515	intron-variant	Abtb2	Mm_Celera	2:103684123	GAGCTTGAGAAGGGG[A/G]TGCCTGAGTGGCAGG	99382
rs27409710	snp	C/T	0.426035	0.177515	intron-variant	Abtb2	GRCm38.p3	2:103684076	CTGAACATATGTGCA[C/T]GTTGTGGGCGTCCCA	99382
rs27409711	snp	A/G	0.426035	0.177515	intron-variant	Abtb2	GRCm38.p3	2:103684026	CTGGGGCCAAGGCAG[A/G]TTTTTGTTGTCTTCA	99382
rs27409712	snp	C/T	0.426035	0.177515	intron-variant	Abtb2	GRCm38.p3	2:103683798	GTTTCCTCTACAAAA[C/T]GAGACATCCTTGCAG	99382
rs27409713	snp	A/C	0.426035	0.177515	intron-variant	Abtb2	Mm_Celera	2:103683721	TGGGAAGTGGGCTTT[A/C]GTCTCAGCCTGGAGT	99382
rs27409714	snp	C/T	0.426035	0.177515	intron-variant	Abtb2	GRCm38.p3	2:103683674	TAATATATTTCTTTA[C/T]CAGGGCAGATGTGTT	99382
rs27409715	snp	A/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103683621	GTGCTCAGACAGATG[A/T]AGGCTCATGTGCAAT	99382
rs27409716	snp	G/T	0.35503	0.226867	intron-variant	Abtb2	Mm_Celera	2:103683608	AAAGGTGGCCTGGGT[G/T]CTCAGACAGATGAAG	99382
rs27409717	snp	A/G	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103683231	GAGCTGCTACCCTAG[A/G]AGAATGTGGGCTGGG	99382
rs27409718	snp	G/T	0.49827	0.0293608	intron-variant	Abtb2	GRCm38.p3	2:103683180	TCCTCCTCAGCCTGT[G/T]GACTCTGGGGTAAAC	99382
rs27409719	snp	A/G	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103683146	AACCAAATTGCTATT[A/G]TGCATCTAGGTGACA	99382
rs27409720	snp	C/G	0.475309	0.108333	intron-variant	Abtb2	GRCm38.p3	2:103683063	ACATTAGCATAAGTT[C/G]TGGAGGAAGACAGCC	99382
rs27409721	snp	C/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103682897	TCCAATGGATGGTGG[C/T]AGCCATTATCTTCCA	99382
rs27409722	snp	C/T	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103682840	TGACTTGACCCTTAG[C/T]GCTGTAAGGACTGAG	99382
rs27409723	snp	A/G	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103682708	AGAGCCCTTATCACA[A/G]TGAAGTTCATGGGCT	99382
rs27409724	snp	A/G	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103682585	GTGGCCTCACACAAT[A/G]ATGGCACATTTCCTG	99382
rs27409725	snp	A/G	0.429688	0.173817	intron-variant	Abtb2	GRCm38.p3	2:103682388	CTGTAGAGTTAGCTG[A/G]GTCCCTAAGGCTTCC	99382
rs27409726	snp	A/G	0.375	0.216506	intron-variant	Abtb2	GRCm38.p3	2:103682299	AGGTGGAAGCTGACT[A/G]GTTAAAGTAATGAAT	99382
rs27409727	snp	A/G	0.48	0.0979796	intron-variant	Abtb2	GRCm38.p3	2:103682278	ATCAGACACCCATTA[A/G]CTGAGAGGTGGAAGC	99382
rs27409728	snp	A/G	0.426035	0.177515	intron-variant	Abtb2	Mm_Celera	2:103682261	AACACAAGAAATACC[A/G]AATCAGACACCCATT	99382
rs27409729	snp	A/G	0.497041	0.0383476	intron-variant	Abtb2	Mm_Celera	2:103682239	GGGAGACTCTGCAGG[A/G]CTCTGGAACACAAGA	99382
rs27409730	snp	C/T	0.426035	0.177515	intron-variant	Abtb2	Mm_Celera	2:103682215	GGCATTTCTGAGCAG[C/T]TTGTGTGAGGGAGAC	99382
rs27409731	snp	A/G	0.345679	0.230967	intron-variant	Abtb2	Mm_Celera	2:103681915	ACCCCACTCTCACCA[A/G]CACTTTTGGCCCTGG	99382
rs27409732	snp	A/G	0.497041	0.0383476	intron-variant	Abtb2	Mm_Celera	2:103681264	GTAGTCCTGTGTTTC[A/G]CCAACTGTTATGACA	99382
rs27409733	snp	C/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103681248	TTGATTTCTCTTTCT[C/T]GTAGTCCTGTGTTTC	99382
rs27409734	snp	A/G	0.497041	0.0383476	intron-variant	Abtb2	Mm_Celera	2:103681191	TCCAGCTCTTGGAAC[A/G]GTATCTCAGCACAGC	99382
rs27409735	snp	A/G	0.35503	0.226867	intron-variant	Abtb2	Mm_Celera	2:103681051	GAGGAAGCTCCAGGA[A/G]CAGCTACTTCTCTGG	99382
rs27409736	snp	A/G	0.297521	0.245442	intron-variant	Abtb2	Mm_Celera	2:103681032	TGTGTCCTGTTTGCC[A/G]TTAGAGGAAGCTCCA	99382
rs27409737	snp	A/G	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103681012	TTTCTGAACCTCTGA[A/G]CCCCTGTGTCCTGTT	99382
rs27409738	snp	G/T	0.444444	0.157135	intron-variant	Abtb2	Mm_Celera	2:103680506	GTGAACTACTAACAG[G/T]TTCGTGGCTGGTACC	99382
rs27409739	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103680163	CGTCAAATGGCTGTG[A/G]ATGTCATTTTTTGTG	99382
rs27409740	snp	A/G	0.473373	0.11227	intron-variant	Abtb2	Mm_Celera	2:103680054	CTCAATTACAGATTA[A/G]AACATTGCAAAATAG	99382
rs27409741	snp	C/T	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103679685	AAAACAAACTTCTCT[C/T]GGAGGGTGGCCAGAT	99382
rs27409742	snp	C/T	0.497041	0.0383476	intron-variant	Abtb2	Mm_Celera	2:103679613	TGGGGAGCTCTGGTC[C/T]TTGGGCTTGCTCTGT	99382
rs27409743	snp	A/G	0.32	0.24	intron-variant	Abtb2	Mm_Celera	2:103679479	GTGATACTTGGCACT[A/G]AGCACCGTGGACCTA	99382
rs27409744	snp	C/T	0.444444	0.157135	intron-variant	Abtb2	Mm_Celera	2:103679478	AGTGATACTTGGCAC[C/T]GAGCACCGTGGACCT	99382
rs27409745	snp	A/G	0.473373	0.11227	intron-variant	Abtb2	Mm_Celera	2:103679331	GCTAGACCAGGCTAT[A/G]TCATACACCACATTG	99382
rs27409746	snp	A/G	0.473373	0.11227	intron-variant	Abtb2	Mm_Celera	2:103679258	GAAGGGGTGAGTTCT[A/G]TCCCACCCAGTTTGG	99382
rs27409747	snp	C/T	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103679166	TCCCAGTGCATAGAA[C/T]GTCCCCCAACACCAA	99382
rs27409748	snp	G/T	0.444444	0.157135	intron-variant	Abtb2	Mm_Celera	2:103679040	TTCTAGTCAAAACAC[G/T]AGCCACCACTTGAAG	99382
rs27409749	snp	C/T	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103679022	TCTTGCCTGTGGCTT[C/T]AGTTCTAGTCAAAAC	99382
rs27409750	snp	A/G	0.142012	0.225474	synonymous-codon	Abtb2	Mm_Celera	2:103678833	CTATGCTCAGCTGGA[A/G]CTTCGGACACTGGAG	99382
rs27409751	snp	C/T	0.497041	0.0383476	intron-variant	Abtb2	Mm_Celera	2:103678691	ACAGTAGCTGTGATA[C/T]GGCGTGCAGAGTTTC	99382
rs27409752	snp	C/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103678677	CCTGAGCCCTGAGCA[C/T]AGTAGCTGTGATATG	99382
rs27409753	snp	A/C	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103678579	TCTCTCTCTTTATGA[A/C]CTCTGAGGCACTAGG	99382
rs29504065	snp	A/G	0.48	0.0979796	utr-variant-3-prime	Abtb2	GRCm38.p3	2:103717675	GGCTGGACTGTTAGG[A/G]GCATGGGCATTCTTA	99382
rs29504874	snp	A/G	0.5	0	intron-variant	Abtb2	GRCm38.p3	2:103653465	GAATGAGATGGGAGG[A/G]TTATAACTTCAAGAT	99382
rs29519964	snp	G/T	0.5	0	intron-variant	Abtb2	GRCm38.p3	2:103670137	GCTTAGCTCTTTCAG[G/T]CCTCAAACTCAGCCA	99382
rs29520655	snp	A/G	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103677504	AGGGAAATGTCACAG[A/G]CTCAGAGGGGAGCAT	99382
rs29523820	snp	A/T	0.5	0	intron-variant	Abtb2	GRCm38.p3	2:103697382	AGTTCCCCAGTTGAG[A/T]GTCTCTCTTCCCAAC	99382
rs29536578	snp	A/G/T	0.5	0	intron-variant	Abtb2	GRCm38.p3	2:103667768	CAAGTTTTTAAACTC[A/G/T]CAAAGCCAATCCCCA	99382
rs29538338	snp	C/T	0.375	0.216506	intron-variant	Abtb2	GRCm38.p3	2:103666134	TTGTCATTCCCATTT[C/T]ACTGTCAAGTAAGCT	99382
rs29538512	snp	A/G	0.5	0	intron-variant	Abtb2	GRCm38.p3	2:103653483	ATAACTTCAAGATCA[A/G]TCTAGGAGATAAAAT	99382
rs29539235	snp	C/T	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103697495	AGACTTCTGTGAGTT[C/T]AGGGCCAACCTGGTC	99382
rs29539769	snp	G/T	0.5	0	intron-variant	Abtb2	GRCm38.p3	2:103637840	GCTACAACAGAGGTA[G/T]TGACAAGGACCTCAA	99382
rs29542520	snp	C/T	0.375	0.216506	intron-variant	Abtb2	GRCm38.p3	2:103669422	AGGGTTGAACGTTCT[C/T]GACCAGCCTGGGGTT	99382
rs29543714	snp	A/T	0.48	0.0979796	intron-variant	Abtb2	GRCm38.p3	2:103635379	CTGTTCTTTACAGTC[A/T]TTATTATATTAAGGT	99382
rs29561282	snp	A/G	0.48	0.0979796	intron-variant	Abtb2	GRCm38.p3	2:103714998	CATATAGACTTATTT[A/G]CTTCCGAGACAGGGT	99382

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