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

Arhgap10

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs6185108	snp	C/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77357795	ACAGTCTTCCCTTTA[C/G]TTTAATACATAAATA	78514
rs6185186	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77357834	AATGTATTTAATAAA[C/T]AGCTTTCCTTACTGT	78514
rs6185625	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77357856	CCTTACTGTTGCTAC[A/G]TAGTGTATAATGGAA	78514
rs6186131	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77357963	taacagccccacggg[C/T]tcatatatttgaang	78514
rs6186140	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77357977	gntcatatatttgaa[C/T]gtttgggcccccgtg	78514
rs6211445	snp	A/G	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77332485	GAGAATGGCTTCCTC[A/G]GAGCTGTATCACCTA	78514
rs6211992	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77332608	TTTGAGACCTTGATA[C/T]GGNGAGCAAGCAGGG	78514
rs6211997	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77332611	GAGACCTTGATANGG[C/T]GAGCAAGCAGGGCAC	78514
rs6212029	snp	G/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77332630	CAAGCAGGGCACCAG[G/T]CTTTACTGGGAAGGC	78514
rs6289772	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77456309	GGACTGGCCTCAAAC[A/G]TTCTTTCAAGTTTTC	78514
rs6289856	snp	A/G	0.5	0	intron-variant	Arhgap10	GRCm38.p3	8:77456361	AGCACCTTACACTGT[A/G]GCTACAAGTAAGTAA	78514
rs6290853	snp	A/G	0.46875	0.121031	intron-variant	Arhgap10	GRCm38.p3	8:77456508	CGCTAGGAACAGCTC[A/G]TGGGCCAACAGTATC	78514
rs6292365	snp	C/T	0.459184	0.136902	intron-variant	Arhgap10	GRCm38.p3	8:77450194	GAAACCCTTGACGCT[C/T]CATTGCTGAGTTCAC	78514
rs6292366	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77450195	AAACCCTTGACGCTN[C/T]ATTGCTGAGTTCACG	78514
rs6292988	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77450332	CCAGACCTGAGTTCT[A/G]GCCACCCTCACAAGA	78514
rs6293019	snp	C/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77450356	CACAAGACAAGAAAT[C/G]CAGACATAAGGCTCA	78514
rs6293472	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77450386	AAAAAGCATCCTTCC[A/G]CTCTCTCNGTCCTGC	78514
rs6293481	snp	G/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77450394	TCCTTCCNCTCTCTC[G/T]GTCCTGCCTTCAGCT	78514
rs6293540	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77450436	TACATGCAAGTCAAA[A/G]GCTCTTGCTAACACA	78514
rs6293568	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77450455	CTTGCTAACACAAAG[C/T]ACAAGNGCCACCCAG	78514
rs6293579	snp	A/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77450461	AACACAAAGNACAAG[A/T]GCCACCCAGCCTTCG	78514
rs6308440	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77332282	GCTGCTTGCCTAAAA[C/T]GATTCAGATGCTACT	78514
rs6386455	snp	G/T	0.429688	0.173817	intron-variant	Arhgap10	Mm_Celera	8:77420425	ACATAAAGGTCTATC[G/T]CCATGCCTGTAACAG	78514
rs6386905	snp	C/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77420479	GGCGGGGGGGCTGTG[C/G]CCCTCACTGGGGTGA	78514
rs6386974	snp	C/T	0.290657	0.246672	intron-variant	Arhgap10	Mm_Celera	8:77420525	AACAGGGCCTCCCAA[C/T]GGTTTAGATGTTTCT	78514
rs6387986	snp	C/T	0.375	0.216506	synonymous-codon	Arhgap10	Mm_Celera	8:77420694	GAGCTTGCACACATA[C/T]TCAAGCGAGAGCTCG	78514
rs6388493	snp	C/T	0.304688	0.243945	intron-variant	Arhgap10	Mm_Celera	8:77420810	CAAGCTGGAGGTCAA[C/T]GGCCTGGTGCTGGCC	78514
rs6389100	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77420964	AAGAGCTTGATGACC[C/T]NCAAAGACTGAAGAT	78514
rs6389102	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77420965	AGAGCTTGATGACCN[C/T]CAAAGACTGAAGATT	78514
rs6389524	snp	A/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77420992	GATTAAGGAAAACAC[A/T]TCTTCCTGGAACAGT	78514
rs13479846	snp	A/T	0.375	0.216506	synonymous-codon, intron-variant	Arhgap10	Mm_Celera	8:77259128	TCTGGGTGAAGGAGG[A/T]GTTCCAGCTGGGTTG	78514
rs32532686	snp	A/G	0.265928	0.249492	intron-variant	Arhgap10	GRCm38.p3	8:77349009	AGAATGAACTACCTC[A/G]TAAGCTGAAAGGCAA	78514
rs32534714	snp	A/C	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77400736	AACTGTGGCTCCTTC[A/C]GATCCCACGCCTAGG	78514
rs32536777	snp	C/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77286450	AGAAAGCACTTCATT[C/G]GTTAGTTTCAGAGGA	78514
rs32538134	snp	C/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77478400	GTTGTCAGGTGCCTG[C/G]TCTAAAACCAAAGAA	78514
rs32542727	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77280701	AAAAGTCTATGCTGG[A/G]AGGCCAGGAAGCCAG	78514
rs32545086	snp	A/C	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77287407	CACAAACAGCTACCA[A/C]ACCATAGTGGCCTCT	78514
rs32548374	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77278741	AAGCATAAGACAAAT[C/T]GTGGGCCCTGAGTAA	78514
rs32548786	snp	G/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77410798	GCCTAGCATAGGAAG[G/T]AGTCTTCTCTTCTAA	78514
rs32556657	snp	A/T	0.48	0.0979796	intron-variant	Arhgap10	Mm_Celera	8:77280015	CCAGAAGCCAAGGAT[A/T]CCTAGACTGCCATTC	78514
rs32556769	snp	C/T	0.48	0.0979796	intron-variant	Arhgap10	GRCm38.p3	8:77451819	AGGCTCCGCCATCAG[C/T]GGTCAGGAAACGGAA	78514
rs32565587	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77351112	AGTTCACCAGCTACC[A/G]GCTTCATTTCATTCC	78514
rs32566013	snp	A/C	0.465374	0.126941	intron-variant	Arhgap10	GRCm38.p3	8:77470451	ACTATCTAACTATCG[A/C]CAGCTCTGATTGCTC	78514
rs32566365	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77334311	ATGAGAAGAGAAAGG[A/G]AAGCTACTTAAGGGA	78514
rs32568156	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77342174	GGACCAAGGGATCAT[A/G]GAGAGCCAAGCCACA	78514
rs32572495	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77331357	CCGTGGCTAAGTCAT[A/G]TCCGCTCTCTAAGCC	78514
rs32573254	snp	C/T	0.48	0.0979796	intron-variant	Arhgap10	GRCm38.p3	8:77444705	TCTTCACTCTGAGCA[C/T]CCTCTATACTGAGCC	78514
rs32573795	snp	A/G	0.493827	0.0552116	intron-variant	Arhgap10	GRCm38.p3	8:77482290	TCCTTTAACCATACT[A/G]TACAGACAGCACAAA	78514
rs32575619	snp	G/T	0.33241	0.236027	intron-variant	Arhgap10	Mm_Celera	8:77314962	TTGGTTATTCCTGTA[G/T]ACTTCTGGCAGCTCC	78514
rs32577176	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484696	GGGCATGGTGGTACA[C/T]GCCTTTAATCCCAGC	78514
rs32577381	snp	C/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77321493	ACCAACGACCCCGAG[C/G]CTTACTCAAAGGTGG	78514
rs32578334	snp	C/T	0.33241	0.236027	intron-variant	Arhgap10	GRCm38.p3	8:77490901	ACACATGCTCTTTAT[C/T]CTTAGGTGTGTGGTG	78514
rs32579538	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77349063	CAGGTAGATGCTACC[A/G]GCTTTGCACAAGTGA	78514
rs32582343	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77509841	CTTGACATTGTTATG[A/G]GCTGAGGTGGGGAAA	78514
rs32583244	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77354753	CTCCCAGCCTCCCAC[C/T]GGGCCACCCATCAGA	78514
rs32585101	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77472169	ATATATATATACACA[C/T]ATATACATATACACA	78514
rs32585804	snp	G/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77479883	GTTGTTGTTGTTGTT[G/T]TTTTTAAATATAGCC	78514
rs32587577	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77435705	ATCCACAGTTCTGGG[A/G]TTCTACCTGAGCTCG	78514
rs32587955	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77490409	TCACATGATTTTTAA[C/T]AGACACTTTTAAACT	78514
rs32589562	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77443006	CTTTTGTGTAGTTTT[A/G]TATCAGGTTTTCGGA	78514
rs32591453	snp	A/G	0.48	0.0979796	intron-variant	Arhgap10	GRCm38.p3	8:77444558	GCGCTGAGCGCATCC[A/G]CTCAAGAAGACCAAA	78514
rs32593254	snp	A/T	0.48	0.0979796	intron-variant	Arhgap10	GRCm38.p3	8:77465421	CCCCACAGGCCTGAA[A/T]CTACCTTCCCCTACT	78514
rs32595629	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77338503	CTAGCACTCTTCCCA[C/T]TGGCTGACTCCTAGC	78514
rs32596259	snp	A/G	0.48	0.0979796	intron-variant	Arhgap10	Mm_Celera	8:77310485	ACAAGTCTCCCAAAA[A/G]AGAAATTTAAGCTGT	78514
rs32598934	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77357065	TCAAAGACCAGCAAG[C/T]ACAGGAATTATCAAT	78514
rs32603497	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77428181	GCCCTCCCCAGAAGC[A/G]ACTGTGACAGACCTG	78514
rs32603831	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77371455	GCTGGGGAGATGGTT[C/T]AGTAAGCGAACTTAT	78514
rs32604318	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77367815	AGAAACACACAGAGA[C/T]GAAGTTAAGAATGTC	78514
rs32614335	snp	A/G	0.493827	0.0552116	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485355	AACCAGTTACTCCAC[A/G]GACCACGAGAAACAG	78514
rs32615022	snp	A/C	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77328863	GACAGACCACCACAG[A/C]GTAAGGCCTGAACAG	78514
rs32617658	snp	G/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77509515	GAGGAAGAGGAAGAG[G/T]GAAAAGAAAATAGGG	78514
rs32620956	snp	A/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77428851	TCTTACTAAGACTTT[A/T]ACATTTTCATAAAAA	78514
rs32621134	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77357025	CTTGCAGGGGGCAGG[A/G]AGGACTGTATGCCTT	78514
rs32623142	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77410080	AAAATGGAAGCTATC[A/G]CTAAGGAGAACTGCC	78514
rs32623496	snp	A/G	0.46875	0.121031	intron-variant	Arhgap10	GRCm38.p3	8:77508069	TCACATTAATATGTC[A/G]ATGGCATCCCGCTCC	78514
rs32627264	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77304677	CGGTCGTGAGAACGC[A/G]TGTAAGAAGGTAACC	78514
rs32627635	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77321443	TGAGCATACATCACC[C/T]CCCAAAGCAGAGCCT	78514
rs32631717	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77352148	GTGGTCCCCAACCCC[C/T]TTGGGGCTGGATATC	78514
rs32633665	snp	C/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77336953	AAACATATTTATCAG[C/T]TAAGGAACAGGCTTT	78514
rs32635041	snp	A/T	0.32	0.24	intron-variant	Arhgap10	GRCm38.p3	8:77464941	AATAGATCTTTTTTT[A/T]AAAAAAGTGCCTTAC	78514
rs32635049	snp	C/T	0.345679	0.230967	intron-variant	Arhgap10	Mm_Celera	8:77408946	ACTACACACACCAAA[C/T]AGCTTTATCTAAAAT	78514
rs32637461	snp	A/G	0.48	0.0979796	intron-variant	Arhgap10	Mm_Celera	8:77333415	AAAGACAGAGCCAGC[A/G]TTTCTTCATTACCCT	78514
rs32644816	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77262910	TGGAGAATAGGAAAC[A/G]TTGATGAGAGGAGAT	78514
rs32645327	snp	A/C/G	0.625	0.125	intron-variant	Arhgap10	GRCm38.p3	8:77477025	ATGTTGAAGCCCTAC[A/C/G]CCCCTTCTCCCCAGT	78514
rs32646960	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77426068	GGGACTAGAGGTGTG[C/T]GCCACTGTGCCCTGT	78514
rs32650619	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77277508	TCAGAGCTGTTATAG[C/T]GTGGATATTGAATGT	78514
rs32650977	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77442479	TGAGATAGTCAACCC[A/G]GCTGGTTCCAATAAC	78514
rs32651306	snp	G/T	0.401235	0.199068	intron-variant	Arhgap10	GRCm38.p3	8:77358791	GACTGCAGAAAGCCT[G/T]CGGGAAAGACAAAAG	78514
rs32651894	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77344871	GCATTCAATAATCTG[C/T]ATTTTCCTTAACAAT	78514
rs32655111	snp	G/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77484317	TCAATCTCATACTTA[G/T]GCTCCCAATTTTCTA	78514
rs32655825	snp	A/C	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77371697	TCCCAGGTCTGCTCT[A/C]CACCCCTTACGCACA	78514
rs32655921	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77337143	TGAGGGCGCTGGCAG[C/T]GAGGCTGAAGAGATC	78514
rs32659469	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77508147	TTTTTTTTTTTTTTT[C/T]TCTCTTTTGATAGAA	78514
rs32660734	snp	A/G	0.48	0.0979796	intron-variant	Arhgap10	GRCm38.p3	8:77443289	TTTATACCATTTATG[A/G]TGTAAATTCACATTC	78514
rs32664122	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77455270	TGCTTTCACATAACG[C/T]AGAAGCACCTGCCAG	78514
rs32667461	snp	C/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77429737	AAAGCTGGATGGGGT[C/G]CATCCCAGATCTCTG	78514
rs32670959	snp	A/G	0.387812	0.208586	intron-variant	Arhgap10	Mm_Celera	8:77329413	TACAGGGCTAGGTTC[A/G]GAGAAAATCAAGATG	78514
rs32689698	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77450237	AAAGCGCCAGGCCCT[C/T]GGAGCACACTGAATG	78514
rs32693085	snp	C/T	0.495868	0.0452663	intron-variant	Arhgap10	GRCm38.p3	8:77510656	GGTGTAGGCCAGGAC[C/T]GCCCACCAGCTCTGG	78514
rs32693201	snp	G/T	0.493827	0.0552116	intron-variant	Arhgap10	Mm_Celera	8:77408798	ACAACTAGTCTTCAG[G/T]GAATTTACTCATGGG	78514
rs32700260	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77366345	AAGATGGTGTGAACA[C/T]ACGTTTGTAACTCAT	78514
rs32704269	snp	C/T	0.277778	0.248452	intron-variant	Arhgap10	Mm_Celera	8:77385630	TGTACGGTCTAATGG[C/T]ATGCTATCATGCACT	78514
rs32706291	snp	A/G	0.484429	0.0868505	intron-variant	Arhgap10	Mm_Celera	8:77371524	CCCGTGTAAAACAAA[A/G]CATTACCGACAACTA	78514
rs32706874	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77324743	TGCTAATAACTTAAA[C/T]TGAAGAAAAAAAATT	78514
rs32707139	snp	A/C	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77508841	ATAGTGAGACTATCT[A/C]CTTAAGATATAATAA	78514
rs32707316	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77428756	CAACATCCCAGTTAG[C/T]GGGGTAAACAGCAAC	78514
rs32707837	snp	A/G	0.5	0	intron-variant	Arhgap10	GRCm38.p3	8:77366640	GTGGCTACAGTGCAC[A/G]CTGCCATGCTTGGCT	78514
rs32707909	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77440241	TCTTCAAAATGAGCA[C/T]CTCATCACCAACAAA	78514
rs32710182	snp	G/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77434986	GTGAAGGGGTCAGGG[G/T]GAGCAGATTCCAGCC	78514
rs32712796	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77418347	GGTTCCTGTGTCATT[C/T]CAGAGCCTGGGCTAA	78514
rs32720656	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77475029	ACTACTAGCCTCCAA[A/G]GTCTGGTTGCCTCGG	78514
rs32720657	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77292083	ATCATGATCACAATT[A/G]CATTTCACACATAAA	78514
rs32723261	snp	A/G	0.415225	0.187619	intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77485654	TGGCAATGGAGCAAG[A/G]TGCCAGCATTAAGCA	78514
rs32725454	snp	A/G	0.48	0.0979796	intron-variant	Arhgap10	GRCm38.p3	8:77333146	TTTGTCCACGTGTAT[A/G]TCTGTGCACCATATG	78514
rs32725637	snp	C/T	0.5	0	intron-variant	Arhgap10	GRCm38.p3	8:77325727	GCATTTCTCCAAAGA[C/T]TTGAGAGGAAGTCTG	78514
rs32726590	snp	A/G	0.32	0.24	intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77502597	ATTTTGCAAGGATGA[A/G]GCAAAAAGGCAACCA	78514
rs32728551	snp	A/G	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77388479	ATGGCCCCAGTGTGC[A/G]TGTGCTGCAGCTGAC	78514
rs32732293	snp	C/T	0.290657	0.246672	intron-variant	Arhgap10	GRCm38.p3	8:77470284	TGCCCGAAGCTGCTT[C/T]GTGGGTAGAAAAGTA	78514
rs32735568	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77257490	CTCCTCCCCATTTCC[C/T]AGTCTCATTTACATG	78514
rs32736131	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77467357	AGCCGGACAGTGGTG[A/G]TACACGCCTTTAGTC	78514
rs32745269	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77413340	TGGCTGCGGAGCTCC[A/G]TGCTACTGCAGAAGC	78514
rs32745986	snp	C/G/T	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77265681	AGGGTGGCCATGACT[C/G/T]GTGCCATGGAGCAAT	78514
rs32748574	snp	C/T	0.46281	0.131194	intron-variant	Arhgap10	GRCm38.p3	8:77447610	GCTCACCTACAGCTC[C/T]GCCCGTCTGCTCTCA	78514
rs32750266	snp	A/G/T	0.459184	0.136902	intron-variant	Arhgap10	GRCm38.p3	8:77405018	GCCTGATGGGCCCTG[A/G/T]CCCAATCGAGTCTCA	78514
rs32754158	snp	A/G	0.426035	0.177515	intron-variant	Arhgap10	GRCm38.p3	8:77478659	CACCATCCCAAGGTC[A/G]AGGCTGTGTTGCCAG	78514
rs32754219	snp	A/G	0.486111	0.0821678	intron-variant	Arhgap10	Mm_Celera	8:77285790	TCAGAAACGGTGGAC[A/G]CTGGCTTGTTTTCTT	78514
rs32754439	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77429586	ACCTGGCCAGTGGGC[A/G]GTATTTCCAGATCCC	78514
rs32758612	snp	C/T	0.48	0.0979796	intron-variant	Arhgap10	GRCm38.p3	8:77481949	TGAGCGCACGGCTTT[C/T]CAAGCACATTCCAGC	78514
rs32762254	snp	A/G	0.48	0.0979796	intron-variant	Arhgap10	GRCm38.p3	8:77443291	TATACCATTTATGAT[A/G]TAAATTCACATTCAT	78514
rs32765178	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77402783	AAGAACTCCGACCTG[A/G]GATGTGCACTTCGAC	78514
rs32769015	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77424228	AGTAGACCAAAAAGT[C/T]AACAGCTGCCCTTGC	78514
rs32772006	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77274034	AGTCCGTAAAGACAA[A/G]GTAAAGAGAAAAGAG	78514
rs32778678	snp	A/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77259766	CACGACCACCCATAA[A/T]GAGATCTGACATCCT	78514
rs32779664	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77508987	GTAAGACTTTCTTAA[C/T]TTAATATATATATAC	78514
rs32779772	snp	A/C	0.495	0.0497494	intron-variant	Arhgap10	Mm_Celera	8:77382495	TGATAGGGCTACAAG[A/C]AGATGTGATTCTATT	78514
rs32782659	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77286284	CTTGTGTCACCACCC[C/T]ACCACAGATACACGT	78514
rs32784892	snp	C/T	0.489796	0.070696	intron-variant	Arhgap10	GRCm38.p3	8:77482022	CCAGAGCAGATTCCG[C/T]AGCCTCAGGGCTTGG	78514
rs32786314	snp	C/G	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77439880	CAGGAGGGCATTAGC[C/G]TACCAAGGACACTGG	78514
rs32786404	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77375996	TTACCAAGAGAACTC[A/G]ACCAAGTTCTCAAGT	78514
rs32786749	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77293421	TAACTTCCTGATAGA[A/G]ACAGGCTTTATACAG	78514
rs32787532	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77321483	GTGTGTGCACACCAA[C/T]GACCCCGAGCCTTAC	78514
rs32787667	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77336995	ACCAGGTTCAAATGT[C/T]GGCTCAGCCACTTTC	78514
rs32792053	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77281809	AATTACTGCCAGACT[C/T]GGAGGCTCTGAAGAG	78514
rs32800487	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77259873	CTTTAAAAAAAAAGC[C/T]AATCTCCCCAAATAG	78514
rs32801726	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77319389	TTTCTCATAATTAAA[C/T]CCTATCTAATAAACT	78514
rs32812533	snp	A/C	0.359862	0.224567	intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77484323	TCATACTTAGGCTCC[A/C]AATTTTCTAAATAAT	78514
rs32825930	snp	G/T	0.375	0.216506	intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77502880	AGCATCACCTATATG[G/T]ATGGGCATGAGAGGA	78514
rs32827556	snp	C/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77368607	CTGCAAATGCTGGCA[C/T]TTAGACAGTGCTTCG	78514
rs32834731	snp	A/C/T	0.475309	0.108333	intron-variant	Arhgap10	GRCm38.p3	8:77330930	TGGCACCATCTACAA[A/C/T]CTGAAGCCCATGGGT	78514
rs32836771	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77251261	AAACAGAGCAGAACA[C/T]GCCTTTCCCACTTCA	78514
rs32842465	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77351681	AAGACTCCTGGAAAA[A/G]AAAAAGAAAAAAAAA	78514
rs32849025	snp	A/T	0.375	0.216506	intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77484436	AGGACACTGTGCAGC[A/T]CACTGCACCCTTGTC	78514
rs32854324	snp	A/G	0.265928	0.249492	intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77502923	AGCAACCCGCTAAGG[A/G]AAAGCACGCCAGTAA	78514
rs32854918	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77429328	CCCAACAAGCGATCC[C/T]GCCCTAGCTATAATC	78514
rs32856578	snp	C/T	0.359862	0.224567	intron-variant	Arhgap10	GRCm38.p3	8:77487526	CAACCAGAAGAACTG[C/T]AGGCACCCTTCACCG	78514
rs32857133	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77381237	GGAGCTGATGCAGAG[A/G]CCATGGAGGAACATA	78514
rs32866280	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77349595	TGTCCAGGGGAAAAC[A/G]ACAGTTTAACCACAA	78514
rs32871718	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77331650	ACCTACTCCTGAGAG[C/T]CTGGAGCCCCCAGGC	78514
rs32873737	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77295981	ATATGCTCAGTCAAG[A/G]GAGTGGCACTATTAG	78514
rs32875025	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77371546	CGACAACTAACATCC[A/G]TGGGTAGCATCTCTG	78514
rs32877174	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77262908	CTTGGAGAATAGGAA[A/G]CGTTGATGAGAGGAG	78514
rs32878274	snp	G/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77418815	GAAAACACAGATATT[G/T]GCATTAGGACTCATA	78514
rs32886772	snp	C/T	0.484429	0.0868505	intron-variant	Arhgap10	Mm_Celera	8:77318339	TTCTCAATATTCTGT[C/T]CTTGGCTACATATAT	78514
rs32889271	snp	A/G	0.48	0.0979796	intron-variant	Arhgap10	Mm_Celera	8:77276851	TCACAGACAGCCCAT[A/G]GGAGTGCGAGCACCC	78514
rs32890907	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77435835	TTCATTGCTGTGAGG[A/G]GACACTATGACCAAG	78514
rs32891172	snp	A/C	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77251430	CCCTTGCACTTCTTC[A/C]CTGGGTAACTCTTCT	78514
rs32892606	snp	A/G/T	0.5	0	intron-variant	Arhgap10	GRCm38.p3	8:77371712	CCACCCCTTACGCAC[A/G/T]TCCCACACGCATGCC	78514
rs32895060	snp	A/G	0.32	0.24	intron-variant	Arhgap10	GRCm38.p3	8:77500805	CAGATACCAGCTTAC[A/G]CTGCAAATACCTTAG	78514
rs32899458	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77429242	CTTTCGTCCTCCAGG[A/G]TCCACTAACACCCTA	78514
rs32904044	snp	C/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77483994	CTTTTGTGACAAGCA[C/T]GCCTTCTATCAGCTC	78514
rs32905139	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77426685	TCTTCATATTCGTTC[A/G]AGTTGAGAGGTAGTG	78514
rs32906572	snp	G/T	0.345679	0.230967	intron-variant	Arhgap10	Mm_Celera	8:77293315	AGCTGCAGGACGCAA[G/T]TGATGACACATGCCA	78514
rs32907571	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77482710	AAATTACACTTAAAA[C/T]GAGTACCTAGACTTT	78514
rs32907920	snp	A/C	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77466728	AGTCCTTAATCAAAA[A/C]AAGTCCCTACAAATT	78514
rs32908483	snp	A/G	0.493827	0.0552116	intron-variant	Arhgap10	Mm_Celera	8:77337351	CTTGGGCGGTGCTGA[A/G]GAGAAACCTCTGAAG	78514
rs32910950	snp	A/C	0.444444	0.157135	intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	GRCm38.p3	8:77515768	CTAGCCCCCCCCCCC[A/C]CACACACACACACAC	78514
rs32912081	snp	A/G	0.5	0	intron-variant	Arhgap10	GRCm38.p3	8:77481071	CTGTCCACGCTGACT[A/G]TCTACACATGAAATG	78514
rs32917355	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77260905	TGCTAACCAGCATAC[A/G]GAAAGTACATTTACC	78514
rs32918042	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77440242	CTTCAAAATGAGCAC[C/T]TCATCACCAACAAAA	78514
rs32918526	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77482769	GTGACCTAGAGCTCT[A/G]TTTCTCAGCACTTGG	78514
rs32921106	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77482107	AAGAGCAGACTGGCC[A/G]ACCACAAAGAAAGAA	78514
rs32924083	snp	A/G	0.304688	0.243945	intron-variant	Arhgap10	Mm_Celera	8:77415372	CCATCTCAGACTTCT[A/G]TGCAGGCAGACTTGG	78514
rs32924806	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77510736	GAGGAGCAGTGGTTT[C/T]CCAGCATGAGAGACA	78514
rs32927176	snp	A/C	0.290657	0.246672	intron-variant	Arhgap10	Mm_Celera	8:77368585	TACTCAGACTACAGG[A/C]AGTTACCTGCAAATG	78514
rs32928651	snp	A/G	0.277778	0.248452	intron-variant	Arhgap10	Mm_Celera	8:77317170	GTACAGAAGATGTCC[A/G]CACAGGAAGCCTACC	78514
rs32928872	snp	C/T	0.290657	0.246672	intron-variant	Arhgap10	Mm_Celera	8:77415041	TGGCATTATTCATTG[C/T]GGTAAGATTCCTCCC	78514
rs32930282	snp	G/T	0.345679	0.230967	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503301	TATTATCCTTGGAAA[G/T]TTTAAAATTGTCCTT	78514
rs32935109	snp	G/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77350599	GGACCTCACAAGAAG[G/T]TAACAGTCAGAGCCA	78514
rs32936274	snp	A/C	0.46875	0.121031	intron-variant	Arhgap10	GRCm38.p3	8:77486178	GATGGCCTTTCAGTC[A/C]GTCTGTCTGTCCATC	78514
rs32940675	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77479858	TGTCAGGCTCAGACC[C/T]GTTTTTGTTGTTGTT	78514
rs32944424	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77331914	TCAATACCGAGCAGC[A/G]AGAAGTGGATGACTT	78514
rs32945797	snp	A/G	0.5	0	intron-variant	Arhgap10	GRCm38.p3	8:77442557	CTCCTGGTTCTGTGG[A/G]CACATGCACAATCCA	78514
rs32960269	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77496141	GTTTTCTATGTATAA[A/G]TAGAAATAACGAATG	78514
rs32963638	snp	A/C	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77290232	AACAAAACAAACAAA[A/C]AAAAAAAAACCAACA	78514
rs32963857	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77412312	TGTGTGTGTGTGTGC[A/G]CACGTTCATGGATAC	78514
rs32970631	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77258665	TCCACTACAAATTGT[C/T]CTCAAGGACCTCCAC	78514
rs32972211	snp	C/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77490872	AAAGCAAGGTCACAA[C/G]AGCCCACAGCAACAC	78514
rs32972389	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77355144	AGCCGCATCCCTCCC[C/T]CCTCCACCTCTAGCT	78514
rs32973197	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77261393	GAGTCACGCCAGAGC[A/G]CAGCTGTCTGGTAGC	78514
rs32973260	snp	A/C	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77251354	CCTACACTATCAACC[A/C]GTGTACCTGAGTCCG	78514
rs32975925	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77319088	TCACTGGAAAGAGAA[A/G]CCCATTGGACTTGCA	78514
rs32976318	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77381209	AACCAAGCAGGACAG[A/G]AACCTGGAGGCAGGA	78514
rs32980887	snp	C/T	0.475309	0.108333	intron-variant	Arhgap10	Mm_Celera	8:77325670	GGCCCCAATATATTT[C/T]TCCACACACATGAGT	78514
rs32988350	snp	C/T	0.391111	0.206368	intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77484869	ACAACACAGGGTAGA[C/T]AGTAACTTCTTCAGA	78514
rs32988987	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77354312	GTCCCTCCCAATAGC[C/T]ACAACCCAGAGAACT	78514
rs32989609	snp	C/T	0.489796	0.070696	intron-variant	Arhgap10	GRCm38.p3	8:77508015	CAGCAAACCCATCCA[C/T]CACATGACAAAGGTA	78514
rs32991500	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77479769	ACAGTAAGATGTGAA[C/T]TGTGTCTGCTGGTCT	78514
rs33003411	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77428782	GCAACTGAGGAGGGC[A/G]TGGCCACCTACCTCA	78514
rs33005652	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77486044	AACATGAGGAACTGT[A/G]TTAAAGGGCAGCATC	78514
rs33006174	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77337290	GCTAGGCCTGGCACC[A/G]GATCATTTACCACTT	78514
rs33008553	snp	A/G/T	0.48	0.0979796	intron-variant	Arhgap10	GRCm38.p3	8:77465102	GTCAGGCTATGGCTC[A/G/T]CCCAGATCAATCTCA	78514
rs33009455	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77505202	AGTCGGGTGCTCTTA[C/T]CCACTGAGCCATGTC	78514
rs33009516	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77374455	TTGCCACAGAGCCTT[C/T]TGATTCAATATGCCC	78514
rs33010831	snp	A/G	0.487535	0.077957	intron-variant	Arhgap10	Mm_Celera	8:77466896	TAACCTCAGAAAGTA[A/G]AAGTTATAAAGTCAC	78514
rs33013926	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77450476	AGCCACCCAGCCTTC[A/G]GCTGCATAATGAAGA	78514
rs33015155	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77327353	TCCCAGGACTGAAGA[A/G]GTGGAGCTGGGAGAA	78514
rs33017534	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77278496	GTTCTAGGGAAACAG[C/T]ACTAACATGGCCTTG	78514
rs33020674	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77279401	CTACAGAGCTGAGAG[A/G]AACTTGGCTGGTGTG	78514
rs33020714	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77279691	TCTTGAGGTTTTACT[C/T]TCTGATGGGGGATAC	78514
rs33024180	snp	A/T	0.32	0.24	intron-variant	Arhgap10	GRCm38.p3	8:77464942	ATAGATCTTTTTTTT[A/T]AAAAAGTGCCTTACC	78514
rs33024669	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77349746	CTTTCCCAAGAGGCA[C/T]GGAGTACAGAGGAAG	78514
rs33026264	snp	A/G	0.5	0	intron-variant	Arhgap10	GRCm38.p3	8:77477760	TTGGAAAATTACACC[A/G]TGCTAAATTTAGGAT	78514
rs33026709	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77486053	AACTGTGTTAAAGGG[C/T]AGCATCAGGAAGGCT	78514
rs33027373	snp	A/G	0.48	0.0979796	intron-variant	Arhgap10	GRCm38.p3	8:77479162	GAGGTTTCCAGTGTC[A/G]AAACTCCTTCTTAAT	78514
rs33028796	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77356245	CTTCCAGAAGACCCA[A/G]AATCCTTTCCCAGGA	78514
rs33031424	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77444198	AAGAAAACAAAACTC[A/G]GTCTGTTCAAAGGAT	78514
rs33034540	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77286727	ATAACAAAAGAAAAA[A/G]TTGTAAATTATCTTC	78514
rs33037017	snp	A/C	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77381661	TCCGCAAACAATTCA[A/C]ACAAATAGTATATTT	78514
rs33041620	snp	C/T	0.48	0.0979796	intron-variant	Arhgap10	Mm_Celera	8:77414271	GAAGAGACAGAGCAG[C/T]CGCAGGCCACGCAGT	78514
rs33042304	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77321012	CTCACGTGGGAAGAC[A/G]CACACTAAACGTGGG	78514
rs33044981	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77325383	TGCCATGAAGTTGAG[A/G]CTTTTTTCCCTGACT	78514
rs33050185	snp	C/T	0.345679	0.230967	intron-variant	Arhgap10	Mm_Celera	8:77405670	AAATACAGATAGATG[C/T]TCTCTAACCGAGAAA	78514
rs33052286	snp	G/T	0.48	0.0979796	intron-variant	Arhgap10	GRCm38.p3	8:77359564	GACAGCCAGCTGTAC[G/T]CAAGAGAAACCCTGA	78514
rs33053810	snp	C/T	0.48	0.0979796	intron-variant	Arhgap10	Mm_Celera	8:77430715	ACAGAAACCGCCTAG[C/T]GCCATAGATTACATT	78514
rs33055623	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77290849	CTTCACCTGTTCCTC[C/T]TCCTGCTCACCTCTG	78514
rs33058056	snp	A/G	0.401235	0.199068	intron-variant	Arhgap10	Mm_Celera	8:77385620	CCAGATGAGCTGTAC[A/G]GTCTAATGGCATGCT	78514
rs33062772	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77333759	AATCCCTGAATGTAC[A/G]CAGGCAATTTTCTGA	78514
rs33063038	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77428656	AGAAATGAAGCTGTG[C/T]CCCAGAGATCACCAT	78514
rs33067186	snp	C/G	0.475309	0.108333	intron-variant	Arhgap10	Mm_Celera	8:77336697	GGGAGCTGCCATTTC[C/G]ACAGCCAAGTCAATG	78514
rs33067625	snp	A/G	0.33241	0.236027	intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77503399	AACAAAAGCATATAC[A/G]ACCACATACTACCTT	78514
rs33073029	snp	A/G	0.493827	0.0552116	intron-variant	Arhgap10	GRCm38.p3	8:77446430	TACACAGGACCACTT[A/G]ACACCAATGTGGTTA	78514
rs33073937	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77435087	CTGGGGCATAGGACA[C/T]CTAAGGGAACAGAAA	78514
rs33074730	snp	C/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77278034	TGTCCCTGTGCATTC[C/G]TTCACACCGAGTGCG	78514
rs33075331	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77438981	ACCAGTGAGTATTAT[A/G]TTTATTTGGTTGGCC	78514
rs33076197	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77443024	TCAGGTTTTCGGAGA[C/T]GGGGTTAATTTGTCT	78514
rs33078400	snp	A/T	0.32	0.24	intron-variant	Arhgap10	GRCm38.p3	8:77463465	GAGGGCACTAGAGAC[A/T]CTCTGGGACTAGAGA	78514
rs33083323	snp	A/C	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77477759	CTTGGAAAATTACAC[A/C]ATGCTAAATTTAGGA	78514
rs33096541	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77348842	GTATTCTCGTCTGAG[C/T]AACTGCTGGGAGAGG	78514
rs33097053	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77499870	AAGGCTTAAAACTAA[C/T]GCTCTACAATCATGG	78514
rs33097178	snp	C/T	0.48	0.0979796	intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77494581	GCGTTTCCAGCATGT[C/T]CTTGTTCCAGCTGCG	78514
rs33100919	snp	A/G	0.5	0	intron-variant	Arhgap10	GRCm38.p3	8:77443628	AGGAGCACTACCAAA[A/G]AGCAAAAACATTCAT	78514
rs33101183	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77285930	CAATTAAAAGACAGC[A/G]ACTCTCCAAGTGCAT	78514
rs33101999	snp	A/T	0.277778	0.248452	intron-variant	Arhgap10	Mm_Celera	8:77404940	CTGGCTGCAGAAACC[A/T]ATTCTCACTGGTTTC	78514
rs33102878	snp	A/T	0.32	0.24	intron-variant	Arhgap10	GRCm38.p3	8:77464943	TAGATCTTTTTTTTA[A/T]AAAAGTGCCTTACCT	78514
rs33102988	snp	C/T	0.46281	0.131194	intron-variant	Arhgap10	GRCm38.p3	8:77479463	GAAGAGCCTGCTCCA[C/T]ACCAAGTGAGTGACT	78514
rs33103329	snp	C/G	0.391111	0.206368	intron-variant	Arhgap10	GRCm38.p3	8:77498488	GATCACTGCTAAAGG[C/G]GGAAACCCCTAGAGA	78514
rs33105586	snp	A/G	0.265928	0.249492	intron-variant	Arhgap10	GRCm38.p3	8:77350789	ACTGTTGGGGCACCT[A/G]TGAAAACCAATATTG	78514
rs33106365	snp	G/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77357012	CCAAGAAGCACCGCT[G/T]GCAGGGGGCAGGGAG	78514
rs33108767	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77481430	AAATTATATTTTGAT[A/G]GCTTTGCCTCGTGGA	78514
rs33112374	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77331584	TGCAGACACACCCAC[A/G]GTCAGGCTGAGTAGT	78514
rs33112944	snp	C/T	0.5	0	intron-variant	Arhgap10	GRCm38.p3	8:77442839	AAATGAATCCCCAAC[C/T]GGGACATTCCTGACA	78514
rs33112948	snp	A/C	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77373621	ATATTATATTTCTAT[A/C]TACATATTTAATGAG	78514
rs33113150	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77373670	ATATAACCATCCTGC[A/G]ATGTTCTTCAAGGTG	78514
rs33113626	snp	C/T	0.475309	0.108333	intron-variant	Arhgap10	Mm_Celera	8:77331596	CACAGTCAGGCTGAG[C/T]AGTGGAGAACAGAGA	78514
rs33117448	snp	A/C	0.48	0.0979796	intron-variant	Arhgap10	GRCm38.p3	8:77448006	TCTCTATGGGCCAAG[A/C]ATTCAAACACCTGAT	78514
rs33117703	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77426680	TCAACTCTTCATATT[C/T]GTTCGAGTTGAGAGG	78514
rs33118759	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77296471	CAGAGCAGTAAAACC[C/T]TAAGACACTGTCTTA	78514
rs33120261	snp	C/T	0.375	0.216506	missense	Arhgap10	GRCm38.p3	8:77277172	GTGGCATCTCCACAG[C/T]TCCCTCCGTCTGCTG	78514
rs33120366	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77428908	ATAACTGTACATTGC[A/G]CCAGAATTTAGGTTT	78514
rs33120717	snp	C/G	0.475309	0.108333	intron-variant	Arhgap10	Mm_Celera	8:77513369	GTCTCCGGGGTCCAC[C/G]AGAGCATCTGCACGT	78514
rs33123452	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77371711	TCCACCCCTTACGCA[C/T]ATCCCACACGCATGC	78514
rs33126102	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77405897	CTGAATTCATATGTG[C/T]ATATAAAATGCTGGG	78514
rs33128395	snp	A/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77480759	TAAGAACAAAGGTTC[A/T]TAACTCCTGAGCTGT	78514
rs33134933	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77426290	CACAGGTAAAATACA[C/T]TTTTAAAAGGGCAAA	78514
rs33141762	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77442950	CATCATTTTCAAAGA[A/G]AGAAAGAAACCTTTG	78514
rs33150079	snp	A/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77484311	TAGTTCTCAATCTCA[A/T]ACTTAGGCTCCCAAT	78514
rs33150796	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77377249	AAAAAAGAATTACTG[A/G]TTTTGCATTATAGTA	78514
rs33156023	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77429339	ATCCTGCCCTAGCTA[C/T]AATCCCTCTCCGAGT	78514
rs33156176	snp	A/C	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77509358	TTAACCTCAGGAAAC[A/C]CAGAGAAGAAAATCT	78514
rs33159017	snp	A/C	0.459184	0.136902	intron-variant	Arhgap10	Mm_Celera	8:77328918	AAGAGGCCACATGTT[A/C]AAAGCCAGTTACCTG	78514
rs33161424	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77434947	TCATCAACGCAGTGA[C/T]ATCTAGGCTAAGTGC	78514
rs33167140	snp	A/G	0.46875	0.121031	intron-variant	Arhgap10	Mm_Celera	8:77316841	ACCTGCACACGTTCG[A/G]GAAGCCCAGCACTGC	78514
rs33173928	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77349549	TCAACTGAGCTCACC[A/G]ACACAGAGCAAAGCC	78514
rs33176523	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77474622	CAGAAAACCAGACAA[A/G]GAATAATGAAATCCA	78514
rs33179572	snp	A/C	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77358904	ACTCAGCTTAGGGCG[A/C]GTGCACGGGGCTTGT	78514
rs33182182	snp	A/G	0.42	0.183303	intron-variant	Arhgap10	GRCm38.p3	8:77465237	AGGCAGACAGAGTGA[A/G]CTGTTGTAAGTACTA	78514
rs33182323	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77279789	CACCAGGATGACTGT[A/G]TGTATCCCTTCAAAC	78514
rs33182514	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77381153	TTTATTGGCTTAGGC[A/G]TCTGTCCGTGGCACC	78514
rs33183936	snp	A/G	0.32	0.24	intron-variant	Arhgap10	GRCm38.p3	8:77479045	GCTCTGCTCAGGCCC[A/G]CCCTTCCCTCACTCC	78514
rs33188100	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77435038	ATTAAGGCATAGTGA[C/T]TGCTTATGCCTGTAC	78514
rs33188608	snp	G/T	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77452053	CGGCATGACTCATCC[G/T]GTCATAAGAGTTGGG	78514
rs33197220	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77510645	CAGGACTCACAGGTG[C/T]AGGCCAGGACTGCCC	78514
rs33197407	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77318422	TTTAACTTAAAATAC[A/G]TAGATCATGTATTGC	78514
rs33206455	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77281588	CAGGCACATCATGGA[C/T]AAAACTTAACAGTTA	78514
rs33207873	snp	A/C	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77480765	CAAAGGTTCTTAACT[A/C]CTGAGCTGTCTCTCC	78514
rs33208872	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77404926	GTGTGCCACCAAGCC[C/T]GGCTGCAGAAACCTA	78514
rs33213637	snp	A/C	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77482809	CCAGAAATAACCAGA[A/C]ACTTATTTTGCTCTC	78514
rs33214555	snp	A/T	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77490414	TGATTTTTAACAGAC[A/T]CTTTTAAACTTCTCC	78514
rs33217952	snp	A/C	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77251483	CCTCTTGAGGGAGGC[A/C]TGCTTCAACCCATCA	78514
rs33222372	snp	G/T	0.207612	0.24638	intron-variant	Arhgap10	Mm_Celera	8:77368643	GCACTGCGGCTGGTA[G/T]CTCAGCTGCCAAGAC	78514
rs33223082	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77386739	TCTTAGGAAGGAAGG[A/G]AGGGAGGGAGGGAGG	78514
rs33227679	snp	A/G	0.33241	0.236027	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503237	TTGGGACTGTCTAAT[A/G]TTACTGCCCCATTTT	78514
rs33229791	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77297897	GGCTCCCACAGACTC[A/G]TGTGTTTGAAACCTT	78514
rs33232094	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77296260	CGTTGGTCAGGGGCT[A/G]GAGAGATGGCTCAGT	78514
rs33233455	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77281939	AACAAAAAACAAAAA[C/T]GGGACCACACTAGGG	78514
rs33233664	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77278664	CACATAAATGCCAAG[A/G]TTGGAAGAAAACTCA	78514
rs33240793	snp	C/T	0.48	0.0979796	intron-variant	Arhgap10	Mm_Celera	8:77316139	CCTATCACAGGAAAC[C/T]GGAGAGGGACTTTAG	78514
rs33244305	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77266163	GGCTCATGCTGCCAT[A/G]CTGACCGTGGGCTTG	78514
rs33246223	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77358655	GAACAGCAAGGGGGG[A/G]AAAAAATTAAAAACC	78514
rs33247573	snp	C/T	0.5	0	intron-variant	Arhgap10	GRCm38.p3	8:77491448	CTCTGGCTCCTGCTA[C/T]ACTACCAGTACTGCA	78514
rs33248295	snp	C/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77426078	GTGTGTGCCACTGTG[C/G]CCTGTATGAGTAGCT	78514
rs33248347	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77413654	AAAAAAATACAGATT[C/T]CAACATCTATGATTT	78514
rs33252397	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77428467	CACAACTCGAATCAA[C/T]GGACCTCTTAAAGGG	78514
rs33253352	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77429278	AGTGGACCCAGACCC[A/G]AGGGTGCCCACCCCC	78514
rs33253839	snp	G/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77478480	CGTGTCAAACAGCCA[G/T]TAAAGTCTAAAGTGA	78514
rs33254024	snp	A/G	0.48	0.0979796	intron-variant	Arhgap10	Mm_Celera	8:77325077	GAGAAGGACGCAGGC[A/G]TGTGGACAGTGTTCC	78514
rs33257352	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77437098	AGGTGGGCACATGTC[A/G]CATCACACACGTGGA	78514
rs33266188	snp	G/T	0.33241	0.236027	intron-variant	Arhgap10	Mm_Celera	8:77328830	GGAGTGTCATCTTTG[G/T]TTGGACAAGGCTGCT	78514
rs33267032	snp	C/T	0.48	0.0979796	intron-variant	Arhgap10	Mm_Celera	8:77267234	GAAAGCATCCATGCC[C/T]GCAGTCTTAAGGAAT	78514
rs33270520	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77453865	AAGCCTATGCATCCT[C/T]TTCCTCCACGAACAA	78514
rs33272034	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77332142	GTTCCTGCTGTAGCC[A/G]TTAGCGGACATCCAG	78514
rs33277308	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77477020	TGCCTATGTTGAAGC[C/T]CTACACCCCTTCTCC	78514
rs33280502	snp	A/C	0.484429	0.0868505	intron-variant	Arhgap10	GRCm38.p3	8:77346446	ACAGACTGCCCTTAA[A/C]GACGATTGATAACAG	78514
rs33281387	snp	G/T	0.408163	0.193609	intron-variant	Arhgap10	Mm_Celera	8:77337321	AGGTTTTGAAATTAT[G/T]ATTCCCAATCCTGTC	78514
rs33285236	snp	C/G	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77490415	GATTTTTAACAGACA[C/G]TTTTAAACTTCTCCC	78514
rs33286321	snp	C/T	0.5	0	intron-variant	Arhgap10	GRCm38.p3	8:77481343	GATCAAAGTTCTATC[C/T]TCCTCAGGGTGAGTG	78514
rs33286686	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77315674	ACAAAGTACACTCTG[C/T]ACATATACTAGTGGC	78514
rs33289067	snp	A/G/T	0.456747	0.140554	intron-variant	Arhgap10	GRCm38.p3	8:77496592	CACACCCAAAGACAA[A/G/T]TTGCCTTATTTTTTA	78514
rs33296567	snp	A/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77399048	GTCCAAACACTCTCC[A/T]GCCATGAAAACCTCG	78514
rs33297030	snp	C/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77381184	ATTACAAAAGTAAGA[C/G]AGGACAGGAAACCAA	78514
rs33298188	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77490446	AGGAAAAACAGATGA[C/T]TGTTTTTAAACCCTT	78514
rs33299847	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77324988	CAGGCCAATGCACTG[C/T]AATGCATGGGTTTGT	78514
rs33300866	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77331413	TGCACAACATGCACC[A/G]CCCCGCTACCCTTCT	78514
rs33301591	snp	A/G	0.475309	0.108333	intron-variant	Arhgap10	Mm_Celera	8:77468622	GATGGACGTGACTAT[A/G]GGCCTGGAAGGTATT	78514
rs33304479	snp	G/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77319368	CAGAGACCAGCACAT[G/T]AAGATTTTCTCATAA	78514
rs33304483	snp	A/T	0.486111	0.0821678	intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77484343	TTCTAAATAATTGTG[A/T]ATGATCAGGGAAGAG	78514
rs33317751	snp	A/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77410435	ACCAATGTTCACCTT[A/T]AGCAATCTCTCACAG	78514
rs33319680	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77331787	AGTGCTTCCGAGGGG[C/T]TTTTCATCCGGTGCC	78514
rs33324490	snp	A/G	0.487535	0.077957	intron-variant	Arhgap10	Mm_Celera	8:77336583	AATCTCCAATGTGAG[A/G]TACAGACAACCTAAT	78514
rs33329585	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77279402	TACAGAGCTGAGAGA[A/G]ACTTGGCTGGTGTGG	78514
rs33329586	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77368521	ATCTACCCTACACAT[C/T]CACAACAGGGCCCCA	78514
rs33332088	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77349044	CTTCACAGAGGAAGG[C/T]TTCCAGGTAGATGCT	78514
rs33333213	snp	A/G	0.32	0.24	intron-variant	Arhgap10	GRCm38.p3	8:77500780	ACTCACGGAGCCCTC[A/G]CTCTAGCTCCAGATA	78514
rs33337397	snp	C/G	0.35503	0.226867	intron-variant	Arhgap10	GRCm38.p3	8:77481498	GAGTACCTTAATCAC[C/G]AACACTCCGTTTACA	78514
rs33337991	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77278098	TGACTTCTAATGGTC[C/T]AATTTATCAACATTC	78514
rs33341873	snp	A/G	0.396694	0.202437	intron-variant	Arhgap10	Mm_Celera	8:77479321	TCAAATAACTCTCTC[A/G]GCTCCAGAAGACTAT	78514
rs33342310	snp	A/T	0.493827	0.0552116	intron-variant	Arhgap10	Mm_Celera	8:77328279	ATATGTCTGTACTTG[A/T]CTCTTACATCTGCGG	78514
rs33344446	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77381183	CATTACAAAAGTAAG[A/G]GAGGACAGGAAACCA	78514
rs33349790	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77263835	AAGTACTAATGTTCT[A/G]ACTGTCAGGGGCTCT	78514
rs33352829	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77350217	TTCTCATGACACTGA[C/T]TTGTGGGGATTTAAA	78514
rs33356142	snp	A/C/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77349405	ATGAGAGAAAATGAC[A/C/T]GAGGCCAGAAGCCTC	78514
rs33362186	snp	G/T	0.426035	0.177515	intron-variant	Arhgap10	Mm_Celera	8:77325009	ATGGGTTTGTGAACA[G/T]CAGGGTGGATTAGAA	78514
rs33362331	snp	A/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77338308	TGAGTCACCGCTAGA[A/T]TACCCGTATACCTGA	78514
rs33369477	snp	C/T	0.48	0.0979796	intron-variant	Arhgap10	Mm_Celera	8:77261506	GCCCCAGCATCTGTG[C/T]AGCCCAGGAAAAGCT	78514
rs33370310	snp	A/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77344585	TAACAAAGCTGTGTA[A/T]TAAGTTAACGAGCCA	78514
rs33376566	snp	G/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77282664	CCAGGAGCGATTTGA[G/T]CATCTGCTTGAGCAT	78514
rs33378539	snp	A/G	0.475309	0.108333	intron-variant	Arhgap10	Mm_Celera	8:77339215	CAAGGTATAAAGGTC[A/G]GTCCTAAGACAAACT	78514
rs33382879	snp	A/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77280770	CAAGCATATGCCAGC[A/T]TGCCCAGGTTGTTCT	78514
rs33386135	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77276630	GTCCTACCATGATCC[C/T]TCAGGTGCCATCAGC	78514
rs33387941	snp	A/G	0.444444	0.157135	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493320	AGGAGGAGGAGAAGG[A/G]GGAAAGGAAAAGAAA	78514
rs33388227	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77480808	CAATTTTCAAAACAA[C/T]AGAAAACAAGTTTGT	78514
rs33395683	snp	C/G	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77510710	CTTCTCTCACTGTGA[C/G]AAGGGCCACTGAGGA	78514
rs33404621	snp	C/G	0.401235	0.199068	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484188	ACAGGGAAGACCAAA[C/G]TAAAAGCCAATGCTC	78514
rs33406882	snp	G/T	0.46281	0.131194	intron-variant	Arhgap10	GRCm38.p3	8:77450248	CCCTTGGAGCACACT[G/T]AATGGAGAAGTGGCT	78514
rs33415625	snp	G/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77434960	GACATCTAGGCTAAG[G/T]GCTGAAAGGTGTGAA	78514
rs33415630	snp	C/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77272519	TCCCTCAGTCTCTAC[C/G]TGGCATATCCTGCCC	78514
rs33419552	snp	C/T	0.408163	0.193609	intron-variant	Arhgap10	GRCm38.p3	8:77510358	CAAGACACTTCTACT[C/T]AGAAAGAGCTGGGAA	78514
rs33419982	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77336130	AAAGTATTTCAATAT[C/T]CAGGAAATTACAAGG	78514
rs33420800	snp	C/T	0.459184	0.136902	intron-variant	Arhgap10	GRCm38.p3	8:77366408	GTCAAAATCAGTATT[C/T]TCTTTCTCTTGCAGT	78514
rs33421668	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77251307	AATTGGCCCAGTGCA[C/T]GGGGCCTCTCCTACC	78514
rs33421924	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77509019	CGTGTGTGTGTGTGT[A/G]TATAAAATCAATGAT	78514
rs33423078	snp	A/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77381485	GTCGATGAGACACTA[A/T]CCTGCACAGTCCCAC	78514
rs33424350	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77498112	CTGACTGCAGAAGCA[A/G]CTCCTGCCATAGGCA	78514
rs33426539	snp	C/T	0.277778	0.248452	intron-variant	Arhgap10	GRCm38.p3	8:77351560	TGGGAATATTTAACG[C/T]GTGCACGCCATCAAC	78514
rs33430860	snp	G/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77482704	CCTCAGAAATTACAC[G/T]TAAAACGAGTACCTA	78514
rs33435793	snp	G/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77257236	CATCTATACAAGCTG[G/T]TGTCAAAACTGGGCC	78514
rs33436851	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77507744	ATTCTACACCGCAGC[A/G]GAAAGGAAGCTACCT	78514
rs33437663	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77260371	TCAATGAACTACAAA[C/T]AATTTTCCTTAGAAG	78514
rs33438202	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77286335	AGGATAATATTCTCT[C/T]TAATATCACATAAAA	78514
rs33441460	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77507901	GGGAAAAACAGGCAA[C/T]CGGCCTGAGGTCACA	78514
rs33447714	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77482065	AGCTCCTTTTACTGA[C/T]AGCCACTGCCACAAT	78514
rs33449052	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77475555	CTCCATGGATACCAC[A/G]TACATACGTGGTTCA	78514
rs33451196	snp	A/G	0.304688	0.243945	intron-variant	Arhgap10	GRCm38.p3	8:77415114	AGTGGCTTCACCCAC[A/G]ATGATCTCCTGTTGC	78514
rs33454193	snp	A/G	0.444444	0.157135	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484957	AACCCCAGGCTCCAA[A/G]CTCCGGGAAATGCTA	78514
rs33455594	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77293337	CACATGCCAACCATG[A/G]TTTTTGGGTGCTTCT	78514
rs33457692	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77351559	GTGGGAATATTTAAC[A/G]CGTGCACGCCATCAA	78514
rs33458557	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77470834	CACGTGCATTCAGGC[A/G]CCCACAGGGCCCAGA	78514
rs33459991	snp	A/C	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77264086	GGTTCACATGAGAAC[A/C]TGGCTAAGAGTCTCT	78514
rs33467964	snp	A/G	0.48	0.0979796	intron-variant	Arhgap10	Mm_Celera	8:77277004	GAAACAGAAAGGCAT[A/G]TTCAACAAAGATTTT	78514
rs33467969	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77486051	GGAACTGTGTTAAAG[A/G]GCAGCATCAGGAAGG	78514
rs33468469	snp	A/G	0.35503	0.226867	intron-variant	Arhgap10	Mm_Celera	8:77337306	GATCATTTACCACTT[A/G]GGTTTTGAAATTATT	78514
rs33468850	snp	C/G	0.304688	0.243945	intron-variant	Arhgap10	GRCm38.p3	8:77509331	AGAGATGAAGCATGA[C/G]ATGGTACAGGATTAA	78514
rs33470626	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77256929	AAAACTGCAAAGCAC[A/G]GGGATGGTGCCAGAG	78514
rs33473943	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77405544	CCAGTGCATGCTCTT[A/G]ACCGCTGAGCCACCT	78514
rs33477906	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77429472	TGTGCCAACACTGAC[C/T]AGAGCCACTGTCAAC	78514
rs33478356	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77454047	TCAACTCTTCAGGGT[C/T]CCCAGTGTTGTCTGG	78514
rs33478803	snp	G/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77373817	GCTTATGGTACCCAC[G/T]ATTCTACTCCCTACT	78514
rs33480656	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77279202	CGGAGAAACTCAGTC[C/T]GGACATTAGGGCCAA	78514
rs33484140	snp	A/G	0.387812	0.208586	intron-variant	Arhgap10	Mm_Celera	8:77343957	CTTTGCCCATGCTCC[A/G]GACTGAAGCCCTGCC	78514
rs33485159	snp	A/G	0.32	0.24	intron-variant	Arhgap10	GRCm38.p3	8:77497147	ATATTTATTTAATGT[A/G]TGTGTTTTGCTGGAG	78514
rs33485967	snp	G/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77450569	CCCAGAAATCAGAGC[G/T]CAGAAAACCCCATCC	78514
rs33486139	snp	A/G	0.495868	0.0452663	intron-variant	Arhgap10	Mm_Celera	8:77455013	GGAAGCTGATGTAGC[A/G]TCTCTCAGAATAGGC	78514
rs33486886	snp	A/C	0.456747	0.140554	intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77493766	GAAGGGGCTCGGAAG[A/C]ATCCCATACTGCCAA	78514
rs33491614	snp	C/T	0.46875	0.121031	intron-variant	Arhgap10	Mm_Celera	8:77378364	GCCTTCCAAGGTCTA[C/T]GTATTATTGGAGGAC	78514
rs33493180	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77285953	AAGTGCATTTCTGTA[C/T]TCAAGCAATATGCTG	78514
rs33494246	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77426064	TGCTGGGACTAGAGG[C/T]GTGTGCCACTGTGCC	78514
rs33494758	snp	C/T	0.5	0	intron-variant	Arhgap10	GRCm38.p3	8:77505685	ATGCACAGTCCCCCC[C/T]GAGACACAGTATGTG	78514
rs33497173	snp	C/T	0.265928	0.249492	intron-variant	Arhgap10	GRCm38.p3	8:77330145	GCAGCACCAACACCA[C/T]AGGCTCCTTATGAAG	78514
rs33500025	snp	G/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77325274	TCCAAAGGCCCTTAG[G/T]TCCTCAGGCTGTGAG	78514
rs33500672	snp	A/G	0.375	0.216506	intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77502885	CACCTATATGTATGG[A/G]CATGAGAGGAGAGTC	78514
rs33513119	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484903	AAACTACTTGAATTC[A/G]GTTTAAAAACTGACG	78514
rs33515249	snp	C/T	0.48	0.0979796	intron-variant	Arhgap10	GRCm38.p3	8:77359563	AGACAGCCAGCTGTA[C/T]TCAAGAGAAACCCTG	78514
rs33515354	snp	A/C	0.277778	0.248452	intron-variant	Arhgap10	Mm_Celera	8:77405882	AGTGTTTATGTAAGA[A/C]TGAATTCATATGTGT	78514
rs33515464	snp	C/G	0.277778	0.248452	intron-variant	Arhgap10	GRCm38.p3	8:77487475	CCAGGAGCAAGAGTT[C/G]CAGTGTTTATGAGCC	78514
rs33519618	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77318287	AAAACAACCAATACA[C/T]TCTATGTGGCTACAT	78514
rs33521733	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77450103	ATGAAAATAGTATGT[A/G]GAAACCCAGTGGTAA	78514
rs33524743	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77387775	CGACAATGCCCCTGC[A/G]GCTGAGCCACCAGCC	78514
rs33525830	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77371337	ATGAATGCAATGCAT[A/G]GAGTGAGAAAATACA	78514
rs33527896	snp	A/G	0.408163	0.193609	intron-variant	Arhgap10	Mm_Celera	8:77336760	GCGGAGCTTCGTCCC[A/G]GGTGAGGAGCATCCA	78514
rs33528190	snp	A/C	0.487535	0.077957	intron-variant	Arhgap10	Mm_Celera	8:77401149	CTTTAAAAAAATAGG[A/C]AAGTTCTTTGTGAAT	78514
rs33528783	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77349576	AGCCAGGAGAGCTGT[A/G]ATGTGTCCAGGGGAA	78514
rs33537984	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77462964	GGTGGCCCAGTGGAC[A/G]TTAGAAGCACAGCGA	78514
rs33542715	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77348376	TCACCACACCTCTGT[A/G]TCTATTTATTTATAA	78514
rs33542718	snp	A/C/G	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77408996	GTCAGTAGGCGCCTG[A/C/G]CACGCAGGCAGCACT	78514
rs33542797	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77451218	AATCAGGAACACCCA[C/T]CAGACAGCACTCCTC	78514
rs33546526	snp	A/C	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77318312	CTACATAATGGAACT[A/C]GGCTTCTGGGATTCT	78514
rs33546901	snp	C/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77276676	CCCCATGTAATCAAA[C/G]AAGCTCAAGGTTTTC	78514
rs33549165	snp	A/C	0.5	0	intron-variant	Arhgap10	GRCm38.p3	8:77444197	CAAGAAAACAAAACT[A/C]GGTCTGTTCAAAGGA	78514
rs33551410	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77465904	CCAGGCTAGAGAAGT[A/G]GCTCAGGGGCCAAAA	78514
rs33552099	snp	C/T	0.426035	0.177515	intron-variant	Arhgap10	GRCm38.p3	8:77478534	GCTACTGGGTCTAAA[C/T]TTTACTCTCTCAATT	78514
rs33553049	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77278970	GAAGTTGGTAGCATC[A/G]TGTAACAAGAAGGCC	78514
rs33554578	snp	A/G	0.429688	0.173817	intron-variant	Arhgap10	Mm_Celera	8:77376310	GAGGTTAGCAGGGAC[A/G]TGGATCAGTCCTCCA	78514
rs33556762	snp	A/C	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77316928	CAAATTTTCTCCTCA[A/C]TAGAACTTACTGACA	78514
rs33559086	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77319367	CCAGAGACCAGCACA[C/T]GAAGATTTTCTCATA	78514
rs33561673	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77438003	TGTGTGCAGCCATGC[A/G]GTGAGATATATACTG	78514
rs33567833	snp	C/T	0.290657	0.246672	intron-variant	Arhgap10	Mm_Celera	8:77415080	CTTCCTCCACAAACG[C/T]GTACAACAGATCTAG	78514
rs33573257	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77505452	CAAATTCAACTTCAC[A/G]AGTTGCAAACTGTTA	78514
rs33577463	snp	A/G	0.475309	0.108333	intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77502355	TAGAATTATTTACTG[A/G]AAGATCCAGAAGCCA	78514
rs33579879	snp	C/T	0.265928	0.249492	intron-variant	Arhgap10	GRCm38.p3	8:77498476	ATACAGAAACGAGAT[C/T]ACTGCTAAAGGGGGA	78514
rs33580810	snp	C/T	0.432133	0.171253	intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77484583	ATTTGTATCTCCTTC[C/T]ATTTAAACTTCAGGA	78514
rs33581644	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77426035	CAGAGCTCTGCCTGC[C/T]TCTGCCTCACGAATG	78514
rs33581712	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77480602	AAAAGATTTATCTTA[C/T]GTGGCTGAGTGTTTT	78514
rs33583934	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77256538	ACAACCCTCAGCAAA[C/T]CCTGTGCGCCTGACT	78514
rs33584063	snp	A/C	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77332122	TCCTCAGCCCTGCCA[A/C]AGAGGTTCCTGCTGT	78514
rs33590206	snp	G/T	0.48	0.0979796	intron-variant	Arhgap10	Mm_Celera	8:77316057	CATATGCCTCGTGAG[G/T]CCCTGAGGCTGGACA	78514
rs33593403	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77470200	GTCTCCGCATACTCA[A/G]GAGGGGCTTGATAAC	78514
rs33593587	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77429612	ATCCCTATAATTCTG[A/G]CAACTGAGGGAGAGA	78514
rs33610836	snp	C/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77336826	CAGAAGAGGCAGCAG[C/G]AAGGGGCACCTTCCC	78514
rs33895930	snp	G/T	0.401235	0.199068	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503504	GTAAGTCACATGTAA[G/T]AAGCCATTAGAAACG	78514
rs33895954	snp	C/T	0.357143	0.273994	intron-variant	Arhgap10	GRCm38.p3	8:77504700	AGGATGGTCAGAGTG[C/T]GAGCATGGCACACTG	78514
rs33896100	snp	A/C	0.5	0	intron-variant	Arhgap10	GRCm38.p3	8:77504734	AGCATGGTCACAGTG[A/C]GAGCATGGCACACTG	78514
rs33896283	snp	A/T	0.345679	0.230967	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503467	TGAACACAGAATTTA[A/T]AATACAGACACCCAC	78514
rs33896331	snp	C/G	0.5	0	intron-variant	Arhgap10	GRCm38.p3	8:77504695	TGGCCAGGATGGTCA[C/G]AGTGTGAGCATGGCA	78514
rs33896344	snp	A/G	0.5	0	intron-variant	Arhgap10	GRCm38.p3	8:77403103	CTAAAATATAAACAG[A/G]TAAACTGCGGGGATA	78514
rs33896400	snp	A/C	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77504768	AGCATGGTCACAGTG[A/C]GAGCATGGCACACTG	78514
rs36242322	snp	A/C	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77372266	CCTACCTGTCCCTGG[A/C]TCTCAGCCGTAGCTA	78514
rs36243886	snp	C/T	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77367180	TATTTAAAAGATGCA[C/T]AAACTTCAAATACAT	78514
rs36261068	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77365383	AGTTCCACATGGATA[A/G]GGATGCCCACAGTTA	78514
rs36262977	snp	C/T	0.21875	0.248039	intron-variant	Arhgap10	Mm_Celera	8:77353520	ATGACGAACCACTCA[C/T]ACACCAGGAAACTTT	78514
rs36264286	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77341820	CCACTCACAAACACC[C/T]TTGTCAGCAGATTTA	78514
rs36264775	snp	C/T	0.493827	0.0552116	intron-variant	Arhgap10	Mm_Celera	8:77324649	ACAGCACTACTGATT[C/T]TGATACCAGAATGTT	78514
rs36266361	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77346868	GCATGCCGACAGAAG[A/G]AAAAGTGTGCGTTTT	78514
rs36274447	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77371854	AAAGAGGCAGTCTGG[C/T]TCGTGACAGGAACGA	78514
rs36290982	snp	A/G	0.489796	0.070696	intron-variant	Arhgap10	Mm_Celera	8:77311582	TGGACAAAGTAATAC[A/G]TGTGCCATAAAGAGA	78514
rs36291288	snp	G/T	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77351937	GTTGCATATCTAATC[G/T]TGGAAAGTATCTTTA	78514
rs36314817	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77371667	AAAACATCCGGGTCA[C/T]GCTCACCCCACACCT	78514
rs36315913	snp	C/T	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77322350	GGTCATGTCACACCT[C/T]GATGGCTGCAAGTGA	78514
rs36316873	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77319048	GTGCTTGGCATTCTC[A/G]TTGGAATGAAAGGTT	78514
rs36319924	snp	C/T	0.35503	0.226867	intron-variant	Arhgap10	Mm_Celera	8:77357397	AACTACACAGTAAAA[C/T]GTGGATTCTCACGCA	78514
rs36323142	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77378583	GATCACAGACTGGTA[C/T]CTTCAAAACTGAGAG	78514
rs36324303	snp	G/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77364454	TAGCAAGGCCAAAAT[G/T]ACAGATTAGTTTGAT	78514
rs36331433	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77272901	AAAATGCTAGAAAGA[A/G]GAAGCACAGACTAAT	78514
rs36335190	snp	C/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77296745	CTCTAGCAGACTCAG[C/G]TAAAACACCGGAAGT	78514
rs36340605	snp	C/T	0.408163	0.193609	intron-variant	Arhgap10	Mm_Celera	8:77361299	CACTGGTCACTGCCT[C/T]GAAGCCGAGGTGTGT	78514
rs36341178	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77335324	GAATCAACAGGAACT[C/T]AAGATTGCCTTGATT	78514
rs36344094	snp	C/G	0.396694	0.202437	intron-variant	Arhgap10	Mm_Celera	8:77344309	AAAGCCCTCTCTTGA[C/G]CAAGGGGATAAGACA	78514
rs36347340	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77323950	GCCACTGAAACATGA[A/G]GGCCCATTGCTTACT	78514
rs36348894	snp	C/T	0.408163	0.193609	intron-variant	Arhgap10	GRCm38.p3	8:77347185	GTGTACCTAAGAACT[C/T]GCTAGCCCTGCAGGC	78514
rs36351364	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77326063	CATGTAGCGTATAAA[C/T]GGTGCTGGACAATGC	78514
rs36352101	snp	A/T	0.486111	0.0821678	intron-variant	Arhgap10	Mm_Celera	8:77325782	AAGTAGACAGAAGAA[A/T]GCCCATCACATGCAA	78514
rs36354188	snp	A/G	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77383889	AGAATGAGCCCAGGT[A/G]ATGGCAACTGTTTTG	78514
rs36354859	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77344550	ATTCACAGCGATGAC[A/G]AGACAGCAATACAGA	78514
rs36355519	snp	A/C	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77327579	CTTCTATGTGAACAA[A/C]CACAGTGGCTCTGAA	78514
rs36357537	snp	A/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77383185	CTTTCAGTGAGCATC[A/T]GAGCTTCTGTCTAAC	78514
rs36359836	snp	A/G	0.459184	0.136902	intron-variant	Arhgap10	Mm_Celera	8:77322220	AGGGCTTTCTAGTGG[A/G]CTGGAAACAAGCAAC	78514
rs36369660	snp	A/G	0.408163	0.193609	intron-variant	Arhgap10	Mm_Celera	8:77327907	TGGATCTCATGTACC[A/G]TACATAAGCTTTTAG	78514
rs36371820	snp	C/G	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77384675	ACAATGAGGCTACCC[C/G]ATGGGCATAAAGACG	78514
rs36390447	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77369824	GCCCATCTTCGTGTC[A/G]CCTGTTTACAGTCTC	78514
rs36395277	snp	C/T	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77384890	TGTCATTTTTGTAAA[C/T]TTAGCATTAGACCAT	78514
rs36402080	snp	A/G	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77349074	TACCGGCTTTGCACA[A/G]GTGACACAATCCTTT	78514
rs36411378	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77263602	CCTCTTTATGCCTCT[A/G]CACAGCCAATCATCT	78514
rs36417609	snp	C/T	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77365984	CCCTAACAAATAAGA[C/T]GTTCCAAAATGTGCC	78514
rs36419719	snp	C/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77317422	AAGGCATGGGTTAAA[C/T]CTCCAAAATGTAATG	78514
rs36423414	snp	C/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77333918	GACCAGAAGGCCAGC[C/G]AGGTGCAGAATACCA	78514
rs36423749	snp	A/C	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77378453	GAAGAGGTCTGTGGA[A/C]GTCTTCCACGTTGTT	78514
rs36438408	snp	C/T	0.35503	0.226867	intron-variant	Arhgap10	Mm_Celera	8:77335590	CTGACTGAAAGATAC[C/T]ATGTGTAGTCCAGTG	78514
rs36439755	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77380340	GGACGTGCAGCAGAA[A/G]TTGGCAACAAGTGTT	78514
rs36444706	snp	C/T	0.42	0.183303	intron-variant	Arhgap10	Mm_Celera	8:77363491	TAATGGAACCTTGGG[C/T]TCACCGTTTAGACCT	78514
rs36449269	snp	A/G	0.396694	0.202437	intron-variant	Arhgap10	Mm_Celera	8:77325590	AGAACTAGGACCTCT[A/G]GGGTCAGCCTACTCT	78514
rs36459387	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77365739	TGTGGACTCTCATAG[C/T]TAAGTGACACTCAGA	78514
rs36460101	snp	A/G	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77335373	AGAGTCAAGGAAAGA[A/G]CTTTTCACTGACAGC	78514
rs36461228	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77265732	GACAGAGAGGGAAGC[A/G]TTGAACACCTCTTGA	78514
rs36461785	snp	A/T	0.408163	0.193609	intron-variant	Arhgap10	Mm_Celera	8:77366923	TAAATTTCTAGTTCC[A/T]ACCTGTGTTTAATTC	78514
rs36464716	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77267624	ATAGCAGCTACCTAA[C/T]GGGAGGCCTGAACAT	78514
rs36467428	snp	A/G	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77351008	CTGTCTGCAGCAGGC[A/G]ACTCTCCCCTCACAC	78514
rs36468946	snp	A/G	0.142012	0.225474	intron-variant	Arhgap10	Mm_Celera	8:77368642	TGCACTGCGGCTGGT[A/G]TCTCAGCTGCCAAGA	78514
rs36471110	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77378513	GTTTTACATCACTAC[A/G]CAGTCCATGTGTGCT	78514
rs36485143	snp	G/T	0.297521	0.245442	intron-variant	Arhgap10	Mm_Celera	8:77351147	TGCATCCTATATAAC[G/T]CATTATCAGGTAGTC	78514
rs36490624	snp	G/T	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77363031	CTGTTTGCTCAATGT[G/T]ACTGAAAACACACCA	78514
rs36494763	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77342742	CCCTGGTGACTCAGT[A/G]CATGCTGAGGCTCAA	78514
rs36495407	snp	A/G	0.396694	0.202437	intron-variant	Arhgap10	Mm_Celera	8:77269865	TAGGAACACTTGCCT[A/G]TCCAGGTCTAAGAAG	78514
rs36506127	snp	C/T	0.473373	0.11227	intron-variant	Arhgap10	Mm_Celera	8:77267705	TGTGACAACTGCCAT[C/T]ACCCATTAGGCACCA	78514
rs36510166	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77382967	GTATTTATAGGAGAG[C/T]CTCCACGATGCATAC	78514
rs36513108	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77359324	TTCACTTCAACCTTA[C/T]AAGCCATTCGCTGCC	78514
rs36515969	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77345182	TGGAAGGCTAACATC[A/G]CTGCGGACCTTGCCA	78514
rs36516619	snp	A/G	0.152778	0.230321	intron-variant	Arhgap10	Mm_Celera	8:77325511	AAGGCAGCCTTATAC[A/G]ACAGAAAACTGCCCC	78514
rs36519116	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77331489	TACAGAGCACGCTGT[A/G]TATCTTTTTACAAGA	78514
rs36529796	snp	A/G	0.124444	0.216185	synonymous-codon	Arhgap10	Mm_Celera	8:77344799	CGAGTGACTTGACAC[A/G]CTAATATTGATTTAG	78514
rs36535906	snp	A/T	0.426035	0.177515	intron-variant	Arhgap10	Mm_Celera	8:77340783	CATCTCACATTTCTT[A/T]GTGCCATCTTCTCTG	78514
rs36539098	snp	A/G	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77289341	GGTTAGAAGAAGGAC[A/G]TGTGGAAAAAAAGTA	78514
rs36543975	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77364143	ATACCCAAGTTAAAC[A/G]AGAGGCAGAAAATGG	78514
rs36546204	snp	C/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77352398	AATCAGAACGGTGGC[C/T]GTGTTAGTAACACAC	78514
rs36547232	snp	G/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77345960	TTTGGGAGTTGTTTT[G/T]TACATACAGGGCTGT	78514
rs36552286	snp	G/T	0.132653	0.220748	intron-variant	Arhgap10	Mm_Celera	8:77251079	CACCATGCCACAGGG[G/T]TTCTGGTAGGCTTCA	78514
rs36552943	snp	A/G	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77326524	GGCTGTTCTAAATTC[A/G]CTGGTGTAGGCTCAC	78514
rs36558338	snp	A/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77366373	CATAGCACACTATAC[A/T]CACAAACTTTCATCA	78514
rs36561009	snp	A/T	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77340659	GCTGTTGCACACCCT[A/T]GTCAATTAAGCTGCC	78514
rs36562957	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77329161	GGCCTCTCTGCAAGC[C/T]GGTCACAGTATGCAT	78514
rs36568433	snp	C/T	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77327014	TTTATCTAATGTTTT[C/T]AGGAATTTGGTGAAA	78514
rs36569596	snp	C/T	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77329994	AGATCTGGTGACAGG[C/T]GGAAACCTATAAGCC	78514
rs36571458	snp	C/T	0.489796	0.070696	intron-variant	Arhgap10	Mm_Celera	8:77324222	ATGCATGTGTTTCCA[C/T]CCTTCATCCAACCCT	78514
rs36587072	snp	C/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77358855	GACAAAGTATGGCAT[C/T]TCAACAGGGCAGCTT	78514
rs36588333	snp	C/T	0.21875	0.248039	intron-variant	Arhgap10	Mm_Celera	8:77251812	GAACCAGTTGTGAAA[C/T]GCAGCTTGGGATCAT	78514
rs36588629	snp	C/T	0.244898	0.249948	intron-variant, downstream-variant-500B	Arhgap10	Mm_Celera	8:77358467	AACATTATTGGATAC[C/T]TTGGAGACTTCTCGT	78514
rs36589775	snp	C/G	0.142012	0.225474	intron-variant	Arhgap10	Mm_Celera	8:77266063	CAGACCCTGGGCTAA[C/G]GGTAAGGACAGCTAC	78514
rs36594637	snp	C/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77377587	TGATATGTTGGTTCT[C/G]TCTCTTCAATGCCCA	78514
rs36598003	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77360441	GTGATGGCTATTTTA[C/T]GCCACAACACCACAT	78514
rs36602263	snp	C/G	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77384546	CACCCCTTGCAAAGA[C/G]TCTGGAAGCTCAGAA	78514
rs36609025	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77341940	TACACAAGGGAAGTC[A/G]GAGGAAGCCAGGAAG	78514
rs36609792	snp	C/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77367672	TGAGCCCGGTTCCTT[C/G]CCACACTAAGGGCAC	78514
rs36616018	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77324928	AAGGAATGCATGACT[A/G]AGGCAAAGGCTGAGG	78514
rs36632688	snp	G/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77376435	AATTGTGGCGATGAC[G/T]ACGCTGGCCTGCCTC	78514
rs36636352	snp	A/C	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77339159	GTTTTATGCGAGCAA[A/C]GTTTTATAGTCTCTG	78514
rs36638917	snp	A/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77378735	CACATGCAGAGCAGT[A/T]GTGCTTCACCCCAAG	78514
rs36644171	snp	C/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77351998	AATACAGGCATAGTT[C/T]TGAAAGGCATCTTTA	78514
rs36648866	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77350912	CTCTTAATTACCTAG[C/T]GTGAGTATCCCTCAA	78514
rs36651692	snp	C/T	0.459184	0.136902	intron-variant	Arhgap10	Mm_Celera	8:77322159	CAGACTGGACATGCC[C/T]GGGAACAAATGACAA	78514
rs36652726	snp	A/G	0.426035	0.177515	intron-variant	Arhgap10	Mm_Celera	8:77366825	TCCTTATTTATTTTT[A/G]TAGCTTCTCAAATAG	78514
rs36653136	snp	A/G	0.497778	0.0332592	intron-variant	Arhgap10	Mm_Celera	8:77369894	CACTTGGCTCCAGGG[A/G]ACATTTGTGAAGCTA	78514
rs36655068	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77382637	GCTCCTGGTGTAGCG[C/T]GTAGCCGAGGGCTGT	78514
rs36656216	snp	A/G	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77318625	TACATCTCGAAAGGT[A/G]ACAGAAAATCCATCT	78514
rs36656535	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77368015	TGTCCAAAGGCAGGT[C/T]GGAAATGGCACGGTA	78514
rs36658060	snp	C/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77335013	CGCCCAGGTTCCAGG[C/T]ATAAAATCATGGGCT	78514
rs36658424	snp	A/C	0.459184	0.136902	intron-variant	Arhgap10	Mm_Celera	8:77322131	GAAAACAGCACTGCG[A/C]AACTGTAAAGACCAG	78514
rs36669779	snp	A/G	0.396694	0.202437	intron-variant	Arhgap10	Mm_Celera	8:77318886	AATTAGAAAGAGTAA[A/G]AACAGTCGAGTAAAA	78514
rs36670393	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77343089	TGGATGGAAAGCATA[A/G]ACATACATTACGTAC	78514
rs36673193	snp	C/G	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77291057	AGCTAAAATTCTAGA[C/G]CAGCCACTACAGCAT	78514
rs36678435	snp	A/G	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77384146	TCAGTCCAAGCAAGA[A/G]AATAAAGCCAGGAGC	78514
rs36686024	snp	G/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77262111	CTGTAGCTTTGTATT[G/T]TCCTTTTGTCTCTGT	78514
rs36691037	snp	A/G	0.244898	0.249948	synonymous-codon, intron-variant	Arhgap10	GRCm38.p3	8:77382738	ACCTCGGGTTTCAAC[A/G]GCGCTGATGCATTTT	78514
rs36707841	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77350806	GAAAACCAATATTGC[A/G]AAATCTAGCCAGTGG	78514
rs36712718	snp	A/G	0.132653	0.220748	intron-variant	Arhgap10	Mm_Celera	8:77375053	GACTGAAGCACAGCA[A/G]TCACACACGTGGCCA	78514
rs36721417	snp	A/T	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77354413	TGACATCACAGCCAT[A/T]AGGACAGTTTTCAGG	78514
rs36725308	snp	A/G	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77383555	TGCATCACTATGCTG[A/G]AAGTGAATTTCAATG	78514
rs36729605	snp	C/T	0.48	0.0979796	intron-variant	Arhgap10	Mm_Celera	8:77323496	AACAAAATATGTAAA[C/T]CAAGAAAATCTATCA	78514
rs36739553	snp	A/C	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77360295	AGGAGGAACACTAAA[A/C]GGAAAGGCTGTCCAA	78514
rs36747675	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77353605	GAGCGACTAACGTAA[A/G]AAAGGTGACTTCATT	78514
rs36748855	snp	C/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77365332	TATATTAGCTTCGTA[C/T]GTGAGCTGAGACCCA	78514
rs36761083	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77354555	ACACTGTAGCAGCAC[C/T]GAGAAGGGTATTTCC	78514
rs36765812	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77350774	GGTACAATTTCACCC[A/G]CTGTTGGGGCACCTG	78514
rs36774028	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77383470	ACTGCTCCAGGGCCC[A/G]AGGGACTGTGGCATT	78514
rs36786120	snp	C/T	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77386153	TTACAAAGGCTCAAC[C/T]ATGGTGGTATTTTTT	78514
rs36794876	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77386070	GTCTGTCAGTGGCTC[A/G]GCTCTTTACAGGGCA	78514
rs36800745	snp	A/G	0.35503	0.226867	intron-variant	Arhgap10	Mm_Celera	8:77294184	TCAGCTTGAACGTGT[A/G]AGCAGTGTGCATGTC	78514
rs36807341	snp	C/T	0.408163	0.193609	downstream-variant-500B	Arhgap10	Mm_Celera	8:77249884	TCATAGTCCAAAGGC[C/T]GCAAATACCGAGCTT	78514
rs36814969	snp	A/T	0.132653	0.220748	intron-variant	Arhgap10	Mm_Celera	8:77374263	TTTATTATCTGATCC[A/T]CATGAATCCAATTTC	78514
rs36821043	snp	C/T	0.408163	0.193609	intron-variant	Arhgap10	Mm_Celera	8:77324264	AGCAGATGATGGCTA[C/T]GAACAAAGCAGCCAC	78514
rs36836713	snp	A/G	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77293947	CTTTGAAGACATAAC[A/G]CCTTGGTATTTCTTT	78514
rs36843365	snp	A/G	0.489796	0.070696	intron-variant	Arhgap10	Mm_Celera	8:77370180	GCACGGTACAGATAA[A/G]AGCTTTGATTCCTAG	78514
rs36852349	snp	G/T	0.444444	0.157135	utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250749	AGCAACGCCAGTCAC[G/T]CTCTGCTTCCGCCCA	78514
rs36855266	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77374964	CTTCAAGAAACTGCA[C/T]GGGATCACTCATAAG	78514
rs36857158	snp	C/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77379003	CTGCATGGCATCTCA[C/G]TTTGATTCTCTCAGC	78514
rs36859288	snp	A/T	0.495868	0.0452663	intron-variant	Arhgap10	Mm_Celera	8:77354511	GAAGAAAAGTCTGGG[A/T]GCTAAGTAGAAAGAA	78514
rs36868200	snp	A/G	0.459184	0.136902	intron-variant	Arhgap10	GRCm38.p3	8:77352710	GCCAGGGATAAGGAC[A/G]GTTGCTCCGTGCTGA	78514
rs36869753	snp	C/T	0.244898	0.249948	utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250748	CAGCAACGCCAGTCA[C/T]GCTCTGCTTCCGCCC	78514
rs36872738	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77375433	GCATCTTCCTTTCTT[C/T]GCCCTCTGTCCCTTT	78514
rs36886497	snp	A/C	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77327048	ATTCTCCTTTGACTT[A/C]TTCATGCAGTGTGCA	78514
rs36890082	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77385887	ATTTATGTAAGCAAT[A/G]GATAATCCTTGCACA	78514
rs36895424	snp	C/T	0.35503	0.226867	intron-variant	Arhgap10	Mm_Celera	8:77327518	TGGGAAATCCCGGAG[C/T]GTCTTTCACACGACT	78514
rs36903987	snp	C/T	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77327632	TTAGGTGCTTGTGTT[C/T]ACTCTATGGCTGAAT	78514
rs36907314	snp	C/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77335518	AACAAGCCTAGTTTC[C/T]TTATAGCCTGATTCC	78514
rs36912202	snp	A/C	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77359294	CATGTGAGTGAGAGG[A/C]TATCTGTATGAGCCT	78514
rs36923122	snp	G/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77337696	CTCAGCCCTGCTCCG[G/T]ACTCAGCTCCAACAC	78514
rs36937485	snp	A/G	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77323112	ACTTAACTCATGAGC[A/G]AGAAAATGTGGAACT	78514
rs36940779	snp	C/G	0.277778	0.248452	intron-variant	Arhgap10	Mm_Celera	8:77287190	CAGTCTCTAAGATCA[C/G]AGTAGAAATCAATGG	78514
rs36941207	snp	C/G	0.408163	0.193609	intron-variant	Arhgap10	Mm_Celera	8:77329375	TTTTTAATGACTTTT[C/G]TTGTTTATCCCTATC	78514
rs36944240	snp	C/T	0.152778	0.230321	intron-variant	Arhgap10	Mm_Celera	8:77291194	TTCAGTCCAGCTTCA[C/T]TTAAACACAAACTTA	78514
rs36947659	snp	C/T	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77343224	TCACCTACTTCCCAA[C/T]CAGGCCTGCCAGTAT	78514
rs36951759	snp	A/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77352427	ACACAGCATTTTAGT[A/T]TTCTGCAAACTGCAT	78514
rs36958444	snp	A/C	0.408163	0.193609	intron-variant	Arhgap10	Mm_Celera	8:77324125	TAAGAAGAATGGAGA[A/C]GCTGCCCATCTTTGG	78514
rs36965994	snp	A/T	0.408163	0.193609	intron-variant	Arhgap10	Mm_Celera	8:77340797	TAGTGCCATCTTCTC[A/T]GGGTAACCGTCTCCT	78514
rs36976137	snp	A/G	0.35503	0.226867	intron-variant	Arhgap10	Mm_Celera	8:77339326	CCATTCCATCACACC[A/G]AGAAGTCAAAATAAG	78514
rs36976276	snp	A/G	0.244898	0.249948	intron-variant	Arhgap10	GRCm38.p3	8:77347214	GCCACAGAAGGCCTC[A/G]GATATCAAACATCAA	78514
rs36977314	snp	A/C	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77377967	CCTGTCACACTCTTT[A/C]TAGAAGCGTTCCTCT	78514
rs36978111	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77330716	TTTCCATATATGATG[A/G]AGCCGAACTGACTAC	78514
rs36983714	snp	A/G	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77386095	AGGGCAAGTCAAGCA[A/G]ATCATGAGTTCAAGA	78514
rs36990130	snp	A/C/G	0.473373	0.11227	intron-variant	Arhgap10	GRCm38.p3	8:77288564	TCAGGCTGTCAGAGC[A/C/G]TCATGGGTCCCTCTA	78514
rs37004852	snp	C/G	0.152778	0.230321	intron-variant	Arhgap10	Mm_Celera	8:77363179	GTGCTCAGACACCTA[C/G]ATGCAGATGAACTTA	78514
rs37005789	snp	A/T	0.165289	0.235211	intron-variant	Arhgap10	Mm_Celera	8:77376322	GACATGGATCAGTCC[A/T]CCACTTAGCAAACAT	78514
rs37007119	snp	A/G	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77267785	CATGTGACTTTTCTC[A/G]GAGATTCCCAAACAT	78514
rs37007492	snp	A/G	0.132653	0.220748	intron-variant	Arhgap10	Mm_Celera	8:77375297	GCCATCTGTTTTCAA[A/G]GCAGCCACGACACCA	78514
rs37012548	snp	C/T	0.152778	0.230321	intron-variant	Arhgap10	Mm_Celera	8:77271899	CTAGCAACTCTTCAC[C/T]GGCAATGAAGTCACC	78514
rs37019661	snp	C/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77315433	GTTCGGCTTTGAGGA[C/T]TTTAAGGCTTCCCAT	78514
rs37024714	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77379015	TCAGTTTGATTCTCT[C/T]AGCTTGACACACTGA	78514
rs37028587	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77378820	GGCTTGGGTAAAATG[A/G]CCCCAAAACGCTGGC	78514
rs37032407	snp	C/T	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77315495	GAGCTGGAAAGCATT[C/T]TTGCCAACCTCTCTG	78514
rs37039031	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77362123	CTGAGGAGAGGATTC[A/G]GAAGGAAAAGGAGCT	78514
rs37043171	snp	C/T	0.5	0	utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250699	AATTAAACATCACAA[C/T]CAATGCCCAGTCCTG	78514
rs37046296	snp	A/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77267884	TCCAGGGCTGCTCCA[A/T]GGCTACAGAGGTCAT	78514
rs37053859	snp	C/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77371998	TTACCACCTCTAATC[C/T]GAGTCTCAAATGCAG	78514
rs37060974	snp	C/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77335173	TGAGCTTAATCAAAA[C/T]CATTAAAAGAGCCTG	78514
rs37068119	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77375889	TAGCCACTGCTCTAG[A/G]AAAATAAAGGCATTA	78514
rs37068794	snp	C/T	0.277778	0.248452	intron-variant	Arhgap10	Mm_Celera	8:77263489	CACAGCAGTGTCCCA[C/T]CTGGGTCCCGAGTCT	78514
rs37076006	snp	A/G	0.408163	0.193609	intron-variant	Arhgap10	Mm_Celera	8:77334999	AAAGACAGACAGCGC[A/G]CCCAGGTTCCAGGTA	78514
rs37079711	snp	C/G/T	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77288696	ACGAACCAGAGAAAA[C/G/T]CTAGTGCTCCTCTTA	78514
rs37097048	snp	A/G	0.152778	0.230321	intron-variant	Arhgap10	Mm_Celera	8:77265980	GAGACAGAGGAGAGC[A/G]TGTTCTGAGAGGCTG	78514
rs37097997	snp	C/T	0.277778	0.248452	intron-variant	Arhgap10	Mm_Celera	8:77264817	TAGCTATCATATCAG[C/T]ATGTCTACTTCCAGA	78514
rs37102410	snp	A/G	0.152778	0.230321	intron-variant	Arhgap10	Mm_Celera	8:77348662	CCCTGTAATGCCCAC[A/G]TATCCTTCCTTGTGT	78514
rs37116319	snp	A/G	0.35503	0.226867	intron-variant	Arhgap10	GRCm38.p3	8:77345786	GTTTTAACATTTGCT[A/G]TAACCTGTTTCTTTT	78514
rs37120205	snp	A/G	0.473373	0.11227	intron-variant	Arhgap10	Mm_Celera	8:77369997	CCAAGGAAAAGATGC[A/G]TGAAAGTGGATGGCA	78514
rs37120671	snp	A/G	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77361729	AGACTACCACCGGGC[A/G]CTTCTACCTCATACC	78514
rs37128382	snp	C/G	0.277778	0.248452	intron-variant	Arhgap10	Mm_Celera	8:77335078	TGCTCCAAAGGACCA[C/G]TTTCCACTTAAAGCT	78514
rs37132932	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77323810	GGCTAACAGCTTCTC[A/G]GATCCACTTCTATAT	78514
rs37135222	snp	A/G	0.426035	0.177515	intron-variant	Arhgap10	Mm_Celera	8:77325542	TTGCCATAGTCTATT[A/G]GTTAGCATTGAGATA	78514
rs37138042	snp	A/G	0.396694	0.202437	intron-variant	Arhgap10	Mm_Celera	8:77363791	GTGAGATTAAGAACA[A/G]ATTTCAAGACAATTT	78514
rs37149661	snp	A/G	0.165289	0.235211	intron-variant	Arhgap10	Mm_Celera	8:77267625	TAGCAGCTACCTAAC[A/G]GGAGGCCTGAACATA	78514
rs37153946	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77360363	GAGCTGTAGGCATGG[A/G]CATGACCACAAAGGG	78514
rs37157110	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77356947	CTATAACACCATGAG[A/G]GTAAAAAAGACCACA	78514
rs37169420	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77296885	AAGTGAGTTGGACAC[A/G]CAGGCTCCACTGCGG	78514
rs37175589	snp	A/C/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77339072	AACAAATTAGTAGCA[A/C/T]AAGGCTCCTCATTCC	78514
rs37208581	snp	A/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77383968	ACCTTGACTTGGCAG[A/T]TCCTTCATGTGCTGT	78514
rs37213229	snp	G/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77378292	CCAACCTTGGACTCT[G/T]AGAATGCATTTCAAA	78514
rs37215372	snp	A/C	0.297521	0.245442	intron-variant	Arhgap10	Mm_Celera	8:77263594	TCCCTGGGCCTCTTT[A/C]TGCCTCTGCACAGCC	78514
rs37221432	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77377007	AAGGTCTGTCATGTC[C/T]TTTCTATCCCATGAA	78514
rs37235241	snp	G/T	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77371842	ACTGCACACGGGAAA[G/T]AGGCAGTCTGGCTCG	78514
rs37238308	snp	C/G	0.486111	0.0821678	intron-variant	Arhgap10	Mm_Celera	8:77251808	CCCAGAACCAGTTGT[C/G]AAATGCAGCTTGGGA	78514
rs37240034	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77378150	TATTCCCTGGGCAGC[A/G]GGAACCTGGACAAGT	78514
rs37243934	snp	A/G	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77339897	CTCTTACACAAGCAC[A/G]GGATCTCTTATGACT	78514
rs37250920	snp	A/C	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77348274	ACTTAATTAACCATA[A/C]ACTAAATTCCTGTTA	78514
rs37264215	snp	A/G	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77320861	TGTGACTGTGACATC[A/G]GTGCCAGTGATGAGC	78514
rs37264691	snp	A/C	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77321346	CATAAAAACTAAAGA[A/C]AATCAAGAGACATGA	78514
rs37265991	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77349021	CTCGTAAGCTGAAAG[A/G]CAATAGGCTTCACAG	78514
rs37267062	snp	C/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77331956	CTTACGAATGCCTAC[C/G]GAGCGCAATTCAGAG	78514
rs37269925	snp	C/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77365201	AGGTTATAAGACCAC[C/T]GTGTTTCAAAAGCTA	78514
rs37276161	snp	A/G	0.408163	0.193609	intron-variant	Arhgap10	Mm_Celera	8:77339098	ATTCCAAATGCTAAC[A/G]TGATTTCTTTGGAAA	78514
rs37283037	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77372556	AGATCCCACTCCTCA[A/G]GCACTGGGCACATCT	78514
rs37299772	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77377920	TCATCTCTTCTCCAC[A/G]AACCAGGCGCATGAA	78514
rs37314270	snp	G/T	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77297013	TAAAAACGATTCAGT[G/T]ATTTTTGAATTTTTG	78514
rs37315325	snp	A/G	0.426035	0.177515	intron-variant	Arhgap10	Mm_Celera	8:77271028	AACATTTTTGCTCTG[A/G]GGACCTGCAAATGCC	78514
rs37332418	snp	A/C	0.48	0.0979796	intron-variant	Arhgap10	GRCm38.p3	8:77347158	TATCAGAATGTGAAG[A/C]GGGACCAGAACGTGT	78514
rs37332581	snp	A/G	0.152778	0.230321	intron-variant	Arhgap10	Mm_Celera	8:77363829	CGTGGTAAGCACAGA[A/G]ATACCTGTGTTCAAA	78514
rs37372103	snp	A/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77335924	TCAGTGGTATACTTG[A/T]CCTGTGAGCATCCCC	78514
rs37376357	snp	C/T	0.277778	0.248452	intron-variant	Arhgap10	Mm_Celera	8:77341474	GGCTTGCTCTCTGCT[C/T]TGGGGATGCTCCTGC	78514
rs37388892	snp	A/G	0.165289	0.235211	intron-variant	Arhgap10	Mm_Celera	8:77370330	CAGGAATAAAGAATA[A/G]GACTTTGCCATCTTC	78514
rs37399208	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77337368	AGAAACCTCTGAAGA[C/T]TTCGCAGCTTTGTTT	78514
rs37404829	snp	A/G	0.497778	0.0332592	intron-variant	Arhgap10	Mm_Celera	8:77323796	GAGCCACATGGGATG[A/G]CTAACAGCTTCTCAG	78514
rs37410322	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77264741	TTTAGAGAAACAGGT[A/G]TGCACATCAGGCAAA	78514
rs37416608	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77361582	TGTATCTAAAAGGCA[A/G]TAAAAACCACCTAGT	78514
rs37420793	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77372275	CCCTGGATCTCAGCC[A/G]TAGCTATGACTCACC	78514
rs37423720	snp	C/T	0.426035	0.177515	intron-variant	Arhgap10	Mm_Celera	8:77374317	ATTCAAACATGTCAA[C/T]ATCTCATGCCACCCT	78514
rs37426521	snp	A/C	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77383910	AACTGTTTTGAAGCC[A/C]TGTGTACATCAGACA	78514
rs37458923	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77316197	CACGCTGTGTCTGCG[C/T]GTTCTTCCCACAGTC	78514
rs37483041	snp	C/T	0.165289	0.235211	intron-variant	Arhgap10	Mm_Celera	8:77326028	TCTAACAGAAAGTAA[C/T]AGCACGAGTCGTCCA	78514
rs37485260	snp	C/G	0.35503	0.226867	intron-variant	Arhgap10	Mm_Celera	8:77354633	CTGCCACATGTCTAG[C/G]TGGCAATAGAACTTT	78514
rs37488149	snp	A/G	0.142012	0.225474	intron-variant	Arhgap10	Mm_Celera	8:77370569	AGGGCTGGAGATTCT[A/G]TTGGCCTTGGAAGGC	78514
rs37494824	snp	C/G	0.18	0.24	intron-variant	Arhgap10	Mm_Celera	8:77370337	AAAGAATAAGACTTT[C/G]CCATCTTCAGGAAAA	78514
rs37503498	snp	G/T	0.277778	0.248452	intron-variant	Arhgap10	Mm_Celera	8:77291112	AACTACATCATAGAC[G/T]GCAAAACACTTTAGG	78514
rs37520563	snp	C/T	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77327068	TGCAGTGTGCATCAA[C/T]GTTTTCCCAAATATG	78514
rs37520603	snp	C/G	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77364530	CTTTGAAGCATCTTA[C/G]AGGTTGCATGGCACA	78514
rs37532515	snp	A/T	0.152778	0.230321	intron-variant	Arhgap10	Mm_Celera	8:77336193	TCTGAGAAAGAGCTG[A/T]TCATGTACCCTTTTA	78514
rs37542209	snp	C/T	0.396694	0.202437	intron-variant	Arhgap10	Mm_Celera	8:77356659	TTGCTGCTGAAATAA[C/T]TAAGGGTAACAATAA	78514
rs37586669	snp	C/T	0.426035	0.177515	intron-variant	Arhgap10	Mm_Celera	8:77354588	TTCAATAAAACTGAA[C/T]GTGTGTCTCAGTGTC	78514
rs37591341	snp	G/T	0.132653	0.220748	intron-variant	Arhgap10	Mm_Celera	8:77325576	ATCTCTGACCTTCCA[G/T]AACTAGGACCTCTGG	78514
rs37594670	snp	A/C	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77335467	ATCTACCACGGAGGA[A/C]CCTTCAGGCTGGGTA	78514
rs37600444	snp	C/T	0.497778	0.0332592	intron-variant	Arhgap10	Mm_Celera	8:77385945	GGTAATTCTGCTCCT[C/T]GAACTGGCTCACTAT	78514
rs37607109	snp	C/T	0.336735	0.234472	synonymous-codon	Arhgap10	GRCm38.p3	8:77310873	GGTATCAGGCGAGGT[C/T]CGAAAAATCTGTCAT	78514
rs37614648	snp	G/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77367902	CAAATTCATCAACCT[G/T]CGAGAGCTAGAGTTA	78514
rs37619688	snp	C/T	0.426035	0.177515	intron-variant	Arhgap10	Mm_Celera	8:77382527	TAACTATGACTTCAT[C/T]TGTTACTGCAGTGAA	78514
rs37620990	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77379303	TTTAGTCCTCTTTGC[A/G]TCCCAAAGTCCTTGC	78514
rs37624087	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77353677	GGTCACAAAGCCGAT[C/T]GCTTTCCAAACAGCT	78514
rs37629721	snp	C/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77297062	CAAGTGCTTTTCAGG[C/T]GCCTTATATACAGGT	78514
rs37631520	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77345577	GACTCCACGCAGCTT[C/T]AAACACTTAGATCCG	78514
rs37635104	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77375199	GAGCCTCGGGCACAA[A/G]GCAGAAGTTGGCTCC	78514
rs37645158	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77342657	GAATATAAAATAGTT[A/G]AGCTACTGTCACATT	78514
rs37656192	snp	A/G	0.132653	0.220748	intron-variant	Arhgap10	Mm_Celera	8:77350224	GACACTGACTTGTGG[A/G]GATTTAAAACCTCAT	78514
rs37657956	snp	G/T	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77339401	GGAGAGGCGCTCGAC[G/T]CTTATGTTATATGGC	78514
rs37661510	snp	C/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77385527	AGTATCAGAGTTGAA[C/G]TGAACTTGGGGACAT	78514
rs37661554	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77294737	CTCCGCCACGCTGCA[A/G]GACTACAATAACACA	78514
rs37671337	snp	G/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77346101	ATTCCCACAATCTGT[G/T]AGGACAAAACATAAA	78514
rs37674144	snp	G/T	0.297521	0.245442	intron-variant	Arhgap10	Mm_Celera	8:77349587	CTGTGATGTGTCCAG[G/T]GGAAAACAACAGTTT	78514
rs37733321	snp	C/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77312627	AGGAGATAAAGGTGC[C/T]TGCCTGAACCTCAGA	78514
rs37749851	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77351217	CCATATAAGTGTCTG[C/T]GTGTGAAACCATCTC	78514
rs37767256	snp	A/G	0.244898	0.249948	intron-variant	Arhgap10	GRCm38.p3	8:77347129	CCAGGGAGAACATAC[A/G]GCTTTGCACTGGTTA	78514
rs37772194	snp	C/T	0.197531	0.244432	intron-variant	Arhgap10	Mm_Celera	8:77267528	CCTTTCAGAAAATTA[C/T]AGGCCGTTAGAGATC	78514
rs37776525	snp	A/G	0.152778	0.230321	intron-variant	Arhgap10	Mm_Celera	8:77271728	TCTTCTGTGCAGGGA[A/G]CCTAAAAGGATTACT	78514
rs37784797	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77344366	ATCCAAGGCTAAGAA[C/T]GAAAGTGCTCAATTA	78514
rs37793096	snp	C/T	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77379976	CAGACTGGCTTCCAC[C/T]TGACTGGCACTAGGG	78514
rs37819952	snp	G/T	0.231111	0.249285	intron-variant	Arhgap10	GRCm38.p3	8:77346770	CTCCCCCAGAATTGA[G/T]GCTCAGGTTACATCA	78514
rs37824058	snp	A/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77355665	TGGGATAAAGTGATA[A/T]ACCGAGAGAAGGGGA	78514
rs37826043	snp	C/T	0.35503	0.226867	intron-variant	Arhgap10	Mm_Celera	8:77288766	ACTGCGGCATACGGT[C/T]TTTATGACGCTTACG	78514
rs37841508	snp	C/T	0.277778	0.248452	intron-variant	Arhgap10	Mm_Celera	8:77295754	TTTTCAATTGCTTTT[C/T]ATTACCTAGCTCAAA	78514
rs37856350	snp	C/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77333650	AAAACTTCCATGAAC[C/G]CTGATACCACTCATA	78514
rs37863956	snp	C/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77331924	GCAGCGAGAAGTGGA[C/T]GACTTTTCCTGGCAT	78514
rs37868354	snp	A/G	0.408163	0.193609	intron-variant	Arhgap10	Mm_Celera	8:77370374	AGGCCAGAGAAAAGA[A/G]CCAGACTTGGAAGAT	78514
rs37869264	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77325192	TCTTAGTATACAATC[A/G]GACAGCTATAGATCA	78514
rs37913940	snp	A/G	0.152778	0.230321	intron-variant	Arhgap10	Mm_Celera	8:77271865	GACCTATGATGTCAC[A/G]AACTCCGAGGAGCCT	78514
rs37937260	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77373691	CTTCAAGGTGAAAGC[A/G]TTTAACCCTTTGCCT	78514
rs37938941	snp	G/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77323242	TCACCCACTCCTCTC[G/T]CCTGGTCTCAAGCTA	78514
rs37948839	snp	A/T	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77360091	AGCCATCGCTACAAA[A/T]CTGACGGGCTTCCCA	78514
rs37960874	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77337748	AAAAGCTCACTCCTG[A/G]CAAATTCGTCCGCCT	78514
rs37965631	snp	A/G	0.277778	0.248452	intron-variant	Arhgap10	Mm_Celera	8:77293497	CTTTGTGCAATAGTG[A/G]TCTCCCTGAACTGGG	78514
rs37968663	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77297034	TGAATTTTTGGCATG[C/T]GAACGATAACATCAA	78514
rs37977222	snp	C/T	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77379035	TGACACACTGAGATT[C/T]GCTTTCCCATAAGTC	78514
rs38000634	snp	C/G	0.486111	0.0821678	intron-variant	Arhgap10	Mm_Celera	8:77287004	TTGATAGCCAAAGAA[C/G]AGTCTCAAAGAATTC	78514
rs38007180	snp	C/G/T	0.142012	0.225474	intron-variant	Arhgap10	Mm_Celera	8:77333876	GTAGAAATGGACTTT[C/G/T]CATGTTCAGTGGCCA	78514
rs38011949	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77378008	AGCTTAGACCTCACC[A/G]CTTCCGGTCACTCAG	78514
rs38011992	snp	A/C	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77375817	AGATGAAAACATGAG[A/C]GTGCTGATAACATTC	78514
rs38021290	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77351352	GTAAGGAGAGTGTGA[C/T]GTGGACAGAACCAGT	78514
rs38023304	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77351437	GTATGCACTGAGGTC[C/T]ATGGTTGATCTGTTA	78514
rs38027292	snp	C/T	0.426035	0.177515	intron-variant	Arhgap10	Mm_Celera	8:77317296	CTTGGAAGCTCTGGT[C/T]CCAGAAAACAAATCC	78514
rs38046978	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77339635	CTAACGGGCTCCTTA[C/T]ACCCACAAGGACAAG	78514
rs38063058	snp	A/G	0.142012	0.225474	intron-variant	Arhgap10	Mm_Celera	8:77375559	AAGACACACAAGATG[A/G]CTGAGTCCCAGGAAC	78514
rs38064269	snp	C/T	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77323756	CCCAGTGGCCAGCAA[C/T]GTGGAACTGCTTTTC	78514
rs38080707	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77331846	ACATGGGACTTACTC[A/G]GCCTGTCAGCATGTG	78514
rs38084413	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77371116	AACAGCACATGCTAG[A/G]ATGCGAATCAACATT	78514
rs38095703	snp	C/G	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77251712	CCAAAGCATTTAAGG[C/G]ACCCTAGCTGAAACA	78514
rs38097013	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77380131	CAGGTAGCAGGCCAC[C/T]AGCAATACTAAAGGT	78514
rs38099326	snp	A/G	0.48	0.0979796	intron-variant	Arhgap10	GRCm38.p3	8:77352513	TATCTTTGCCAGGCC[A/G]GGGATGTTAACTGCA	78514
rs38105160	snp	A/G	0.197531	0.244432	intron-variant	Arhgap10	Mm_Celera	8:77364685	GCATGGTTCTGGAGA[A/G]GAGCCTGGTGAGAAC	78514
rs38119701	snp	C/T	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77361069	CCTGGCAGTCCTTCG[C/T]AATCAGTGAGCGAAG	78514
rs38128178	snp	C/T	0.459184	0.136902	intron-variant	Arhgap10	Mm_Celera	8:77321831	CTGGTGACCTCTTCC[C/T]GTAGTCGTAAAAATT	78514
rs38131406	snp	G/T	0.426035	0.177515	intron-variant	Arhgap10	Mm_Celera	8:77316677	ATGCGCACCAGTCAC[G/T]TACTCCTAGCTACAC	78514
rs38139180	snp	C/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77376554	GCTGCAGAATTTCAG[C/G]GATGCATTTGCAGCT	78514
rs38144897	snp	C/T	0.35503	0.226867	intron-variant	Arhgap10	Mm_Celera	8:77372995	AATTTTCTGGAATGA[C/T]CAAGTTGGACAGCGG	78514
rs38145047	snp	A/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77379560	TGTGGAAATGCATTA[A/T]GTACAAGCTTTCAGT	78514
rs38158916	snp	A/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77334945	AGCTTGAGGCAATCC[A/T]TCTGTAACAGGTTAG	78514
rs38232589	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77369797	CTCTGCCACGTGCTA[C/T]CACACAGGGATGCCC	78514
rs38268744	snp	G/T	0.197531	0.244432	intron-variant	Arhgap10	Mm_Celera	8:77267180	TAACTTGCTCACCCT[G/T]CAGCACGAACGTGTA	78514
rs38270548	snp	A/G	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77363887	ATCAGATAAAGCCAG[A/G]GTCACTTTGACCGAC	78514
rs38285978	snp	G/T	0.152778	0.230321	intron-variant	Arhgap10	Mm_Celera	8:77353188	AGCCATATCCAAAGC[G/T]GAATGCAGTGAGTGC	78514
rs38296333	snp	C/T	0.142012	0.225474	intron-variant	Arhgap10	Mm_Celera	8:77346213	CTTGGGGATACACGG[C/T]CCAGCCAAGAACAAC	78514
rs38300065	snp	C/T	0.396694	0.202437	intron-variant	Arhgap10	Mm_Celera	8:77342498	TATGAACCGATCAAC[C/T]CAGGAAGCCATCACC	78514
rs38305283	snp	A/G	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77384590	CCTGGAAAGCTGCCC[A/G]TCATCACTCATGACT	78514
rs38305689	snp	G/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77385739	GTCTGCAGTCTCTAA[G/T]GAACTTGTCACAAGT	78514
rs38318410	snp	A/G	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77383387	GTTTGCTTATGACCA[A/G]GCTGGCATATATTTA	78514
rs38349251	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77380127	ATCCCAGGTAGCAGG[C/T]CACTAGCAATACTAA	78514
rs38351401	snp	C/G	0.35503	0.226867	intron-variant	Arhgap10	Mm_Celera	8:77357311	TGTGCCCGAGCGGCA[C/G]AGCGGGCCACAAGGG	78514
rs38356761	snp	A/T	0.18	0.24	intron-variant	Arhgap10	Mm_Celera	8:77328914	CTCCAAGAGGCCACA[A/T]GTTAAAAGCCAGTTA	78514
rs38358202	snp	A/G	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77336156	CAAGGTCTGAAACCT[A/G]AAACGCTCTGGTCCT	78514
rs38367281	snp	A/G	0.142012	0.225474	intron-variant	Arhgap10	Mm_Celera	8:77267742	TGGTAGATGAGTCTC[A/G]GGTTCCCAGGTCTTG	78514
rs38375041	snp	C/T	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77315138	TGATGTGCTAGCCTA[C/T]AAATGGTGTCTTCCC	78514
rs38384339	snp	A/C	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77336618	ACCTTGGAGCTGCTG[A/C]GCACAACAGTAGCTG	78514
rs38406879	snp	A/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77375516	AAAGGGTGCAAATCC[A/T]ATCAGTTAATTCTGC	78514
rs38429482	snp	C/T	0.197531	0.244432	intron-variant	Arhgap10	GRCm38.p3	8:77356684	CAATAATGTACACAA[C/T]AGTTTAGGAATGAGA	78514
rs38437093	snp	A/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77345853	TTGTCCAACTATGTG[A/T]CCACTGGCACTTTCA	78514
rs38443735	snp	A/C	0.231111	0.249285	intron-variant	Arhgap10	GRCm38.p3	8:77345388	GAGCCAATGATTGGA[A/C]ATGAAAACGGAATCT	78514
rs38467292	snp	C/T	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77367746	GTAGTTTGACCTCAG[C/T]GAAGTCAAGAGCAAG	78514
rs38471581	snp	A/T	0.48	0.0979796	intron-variant	Arhgap10	Mm_Celera	8:77324119	GTGTCTTAAGAAGAA[A/T]GGAGAAGCTGCCCAT	78514
rs38516843	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77329346	TTCCCACTTTTCCAA[C/T]GGCTCTGATGACATT	78514
rs38554033	snp	A/G	0.35503	0.226867	intron-variant	Arhgap10	Mm_Celera	8:77355437	TCAGAAAAGAATATC[A/G]CCTAAATCGTAACTG	78514
rs38581039	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77312328	CTATGACCACACTTT[A/G]ATAACAGCCCCAAAC	78514
rs38589331	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77273635	CAGAGGAGTCAGTGC[A/G]GACTATTTGGAACCC	78514
rs38590688	snp	C/T	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77364691	TTCTGGAGAAGAGCC[C/T]GGTGAGAACTGCAAA	78514
rs38632638	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77310276	CTGCAGGCTTTTGAC[A/G]TGACTGAGAGAACTG	78514
rs38670899	snp	A/G	0.345679	0.230967	intron-variant	Arhgap10	Mm_Celera	8:77273072	AATAATTATCAGTGA[A/G]GGAAATTAAAGAGTA	78514
rs38671066	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77332760	AGGCTGGCATGGTCC[C/T]CTAAAGTGCATGAGC	78514
rs38693989	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77265038	GCAGATGGGTCAGCT[C/T]TGAGCACTGCTGGCA	78514
rs38748666	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77380403	GATGAAGAATCTGAC[A/G]CCTATACACCGTGTA	78514
rs38798085	snp	A/G	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77311881	TCAAGCACGTGACTT[A/G]TGCTGAGTGACAGCG	78514
rs38834449	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77360517	CAGCATTTGATTACC[A/G]CAGCTGACCACAGCA	78514
rs38872978	snp	C/T	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77326614	GTCCTAATTCCTGTG[C/T]TCCAGGCTGTCCTCA	78514
rs38896717	snp	A/G	0.35503	0.226867	intron-variant	Arhgap10	Mm_Celera	8:77360530	CCACAGCTGACCACA[A/G]CAGGCAATGAACTAC	78514
rs38897410	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77379326	GTCCTTGCAGCAATC[C/T]GGTGAGTCTCCAAGC	78514
rs38912520	snp	A/C	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77353631	TCATTCAGAGGTCGC[A/C]GAGGAGCAGGACTCA	78514
rs38919325	snp	A/C	0.297521	0.245442	intron-variant	Arhgap10	Mm_Celera	8:77311608	AGAGAGGCAGACCGC[A/C]CTGCAGTGAGTTATC	78514
rs39137548	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77337760	CTGGCAAATTCGTCC[A/G]CCTCCCTTGTACTTA	78514
rs39144270	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77273556	AGAGAGCAGATGCCT[A/G]AGAGGACTAACTTCT	78514
rs39185818	snp	C/T	0.495868	0.0452663	intron-variant	Arhgap10	Mm_Celera	8:77321794	GAACCGACCAGATAC[C/T]AGATGATCTTACTGT	78514
rs39186344	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77358957	TCCTGAGTAGTCTGT[A/G]AGGAACACTATCACC	78514
rs39205429	snp	C/T	0.197531	0.244432	intron-variant	Arhgap10	Mm_Celera	8:77337610	GGACAGATCTCTGCA[C/T]CTCCGAAACTCCAGA	78514
rs39238648	snp	C/T	0.426035	0.177515	intron-variant	Arhgap10	GRCm38.p3	8:77345052	ACCAGTCTCCTCAGG[C/T]ACAGGCTCCTTCCAT	78514
rs39241180	snp	C/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77364248	CTTGAAACGTGCTTG[C/T]TTATGAAACTCTTGA	78514
rs39286628	snp	A/C	0.345679	0.230967	intron-variant	Arhgap10	Mm_Celera	8:77266900	GGACTTGAAAGCCAG[A/C]GTCTTCTTACCTGAC	78514
rs39417579	snp	G/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77368308	TAAAGTTACAATTTT[G/T]AAATCAGCCTTGAGT	78514
rs39591676	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77322905	CAGCAGGTCTCCACA[A/G]CCATCCTCAGGCCCT	78514
rs39613473	snp	C/G	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77335491	CTGGGTACCCAAGAG[C/G]AACGTCACACTAACA	78514
rs39684420	snp	A/G	0.48	0.0979796	intron-variant	Arhgap10	Mm_Celera	8:77324406	AAGAAGGACTGACAG[A/G]CATAAGAAGGACTGA	78514
rs39686306	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77379545	GCACCTTCACCGTTG[C/T]GTGGAAATGCATTAT	78514
rs39720748	snp	C/T	0.21875	0.248039	intron-variant	Arhgap10	Mm_Celera	8:77332824	GCAAGAATGTACTAG[C/T]CAAAACATTTAGCTT	78514
rs39786791	snp	C/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77340088	GTATGCATACGAATT[C/T]TGTACCTAGGTAGAT	78514
rs39796002	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77380207	AGGACAATGCTTTAT[C/T]AGTGCACCGTAATCA	78514
rs39823400	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77293366	CTATTTCTCACACTG[C/T]TGGAAGTGCTCTGTT	78514
rs39826910	snp	A/G	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77251045	TACAAGCCTGTTCCC[A/G]GTGCTTACCCCTGAC	78514
rs40015843	snp	C/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77338146	GGAGAGTATTCTGTA[C/T]GTGTCCACAGTTTAA	78514
rs40051957	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77355761	ACGTGCGCATGTGAA[C/T]ACGAAGCCCCGATTT	78514
rs40365947	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77335348	CTTGATTAGGACCTG[A/G]AGGGCATCAAGAGTC	78514
rs45632343	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77510810	TAGAAGTCACTGGTA[A/G]TCACCCTTGAGCAAT	78514
rs45637342	snp	A/T	0.152778	0.230321	intron-variant	Arhgap10	Mm_Celera	8:77496058	ACTCCTAGTATCTTC[A/T]TGTACCCTACCACCA	78514
rs45637412	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77471804	TCTGTAACTCAAAAG[C/T]ACACAAGTTAAAACC	78514
rs45645759	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77498533	CAACGGGCTTGTCTC[C/T]GAGATACAAGGACAT	78514
rs45660796	snp	A/G	0.46281	0.131194	intron-variant	Arhgap10	Mm_Celera	8:77460637	CCAGCCCTCAGGCCC[A/G]ACACATTTCTGACTG	78514
rs45664184	snp	A/C	0.408163	0.193609	intron-variant	Arhgap10	Mm_Celera	8:77506164	TGCTGTGGCTTGTGA[A/C]GGATGAAAGTAGTCT	78514
rs45672358	snp	A/C	0.459184	0.136902	intron-variant	Arhgap10	Mm_Celera	8:77456584	CTGACCAATGTGGGT[A/C]ATCTCTGTACTAAGT	78514
rs45678284	snp	A/G	0.152778	0.230321	intron-variant	Arhgap10	Mm_Celera	8:77414157	TCCCACGGGCAGATA[A/G]TGTCCAGGCAGCTAA	78514
rs45686502	snp	C/G	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77420759	CGGCCTGTGTTAAAA[C/G]AAGCACTGTGAGTTG	78514
rs45707200	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77374194	CATTTAAATCACTAT[C/T]ACCCCCTGTATAAAT	78514
rs45708769	snp	A/C	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77513417	CCCACTGCTATAAAA[A/C]GGGAAAACGAACACT	78514
rs45710007	snp	C/G	0.46281	0.131194	intron-variant	Arhgap10	Mm_Celera	8:77456624	CAGAATAAGCAGTAT[C/G]TGAAGTCAAAGGAAT	78514
rs45712843	snp	A/G	0.244898	0.249948	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493567	CGTTCTCTGTTTTCC[A/G]TCCCAGGCATGAAAG	78514
rs45713153	snp	C/G	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77403777	CACGTGGAAGTGCAC[C/G]ATGCAGGTTATCTTA	78514
rs45716759	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77402910	TTCCACTCAGCGTGC[A/T]ACACAAGCACTCTCG	78514
rs45723022	snp	A/G			downstream-variant-500B	Arhgap10	Mm_Celera	8:77249878	CTCCCTTCATAGTCC[A/G]AAGGCTGCAAATACC	78514
rs45727166	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77395669	CCAGCTTTTTTAAAT[A/G]CAAGTTTCCTCTCAG	78514
rs45738168	snp	A/G	0.408163	0.193609	intron-variant	Arhgap10	Mm_Celera	8:77495899	TCTATCAAAATTCTT[A/G]CTACCCCTTCAGAAT	78514
rs45740623	snp	A/C	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77419373	ACAGAAAAAGTAAGT[A/C]CCCTACCATCGGAAC	78514
rs45750212	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77424887	GTCTTCAGTAGCTGA[A/G]GGGAAATGGAGAGTG	78514
rs45750700	snp	G/T	0.345679	0.230967	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503687	CCTCACGGTTCTGAC[G/T]GACGTCAATGGCGCT	78514
rs45751817	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77464493	CGTTATTTTAGATTT[A/T]ATCAAAAATGATTAA	78514
rs45761744	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77374513	AGCCTTAGAAATAGC[A/G]TCCCCTTCCTTTTAT	78514
rs45764764	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77254179	AAGGGGGCAGATTTC[C/T]TCCAGCTTTCAGAGA	78514
rs45769415	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77279039	CCAAGCAGAGAAAGT[A/G]GGGCACACTAGACTG	78514
rs45771790	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77512116	AAAAGGGTCAGGAGT[A/G]AGAGACCAGCAGGCT	78514
rs45772512	snp	A/G	0.124444	0.216185	intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77502288	AAACCAGGAAAGGGC[A/G]TGGTTCTTGTCAACA	78514
rs45772749	snp	A/G	0.244898	0.249948	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494259	ATTTCTATGACTAGA[A/G]AAGGAAACTCTAAGG	78514
rs45776346	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77451283	TTTGAACTGATCACC[A/G]CCACCACCATCACAC	78514
rs45777028	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77451115	CACCATCCCTCCCCT[C/T]CCCACCTCCTGCAGC	78514
rs45782642	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77456728	ATACATATACCTGAC[A/G]GAGAAGCCTTAAAAC	78514
rs45791589	snp	A/C	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77408698	GCATTCTTTCTCCCG[A/C]GATCTTGGCAAACGC	78514
rs45793555	snp	C/T	0.132653	0.220748	intron-variant	Arhgap10	Mm_Celera	8:77488197	TACCCCGCCTCTACT[C/T]TAGTATCACTGCCCT	78514
rs45800498	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77483076	CAAAAGGTAGGGATT[C/T]CTCCATGCTCAGCAA	78514
rs45806044	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77504535	TCCCTGTGACTCTCA[A/G]CAACTGTCTTAGTCA	78514
rs45821551	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77427788	GCTCCCACCTGGCAC[A/G]AGCTGGCACAAGCTA	78514
rs45822064	snp	A/G	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77401491	TGTATGACTACCTAC[A/G]AAATCACTTTCAGCC	78514
rs45827098	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77352964	AAGTACATGTCCTTT[A/T]CTTAAGTGACCATCT	78514
rs45834437	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77449393	cctgtgcacactgcc[A/G]catccctggccctgt	78514
rs45837884	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77448480	ACACACCTGCTGCAG[A/G]CACACAGAGATGTGT	78514
rs45839170	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77420300	TCCCTGTCTGTCACG[C/T]CCTGAAATGAAAGTA	78514
rs45842856	snp	C/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77345610	CCTTCGAACACCCTC[C/G/T]CTCTCTCCTTGCAAT	78514
rs45855607	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77460966	AGACCTCATCACAAA[A/G]TAACCTGGCCTACAA	78514
rs45865786	snp	A/T	0.142012	0.225474	intron-variant	Arhgap10	Mm_Celera	8:77462491	CTGTGAGAGGCCTGG[A/T]AATGTGACATCTCTG	78514
rs45876624	snp	C/T			downstream-variant-500B	Arhgap10	Mm_Celera	8:77250120	AGTCAGGAGGGCTGG[C/T]CATCAGCATAACTAT	78514
rs45885988	snp	C/T	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77487377	CACTAGCTGGACCAA[C/T]AAAGTCCTTTAAAAA	78514
rs45897465	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77507947	AGCTGACCTTATCAC[A/G]GTGACTTGTCACTTA	78514
rs45902463	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77271760	GTCAAGGACCCAGCT[C/T]CATCAATTACAATAG	78514
rs45917799	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77252123	CTCGCTAGGTCCTAA[A/G]TATTGGACACTGCAA	78514
rs45922385	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77276001	GCAGCCAGGACTAGA[C/T]GCTGGGTACCACAGC	78514
rs45943416	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77373172	TCCTTTGATTAGTTA[C/T]GGTTCCTTTGTTTTT	78514
rs45970378	snp	A/G	0.132653	0.220748	intron-variant	Arhgap10	Mm_Celera	8:77387918	TAGGCCAAGCAGGCC[A/G]GGTGGTACCTGCTCT	78514
rs45970417	snp	A/G	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77464403	TCTTTGAAGTAGAAT[A/G]AGAAGAGCAAAGGCA	78514
rs45976667	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77275423	CCCTTCTTCCCGTCT[A/G]TGCAGGCAGCGCCTA	78514
rs45982488	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77501909	GGTTGGACAGAGATA[A/G]AACCCTGACGGGACG	78514
rs45985679	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77345315	TCCTACATGTATTTG[A/C]TCAATATTAAACAGA	78514
rs45988662	snp	A/C/G	0.5	0	intron-variant	Arhgap10	GRCm38.p3	8:77387640	GATAATTTTACCCAG[A/C/G]GATACACTTCTTAAA	78514
rs45997520	snp	A/G	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77496219	AGCAAGGCAGGCCTA[A/G]CAGCAAGTCCCATCA	78514
rs45999900	snp	C/T	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77416069	CAGAGTCCACTGAGG[C/T]TCCAAGATGGGAGTC	78514
rs46003539	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77472021	ACTGAGAGCCTCTAC[C/T]GGCATGCAGTATAGG	78514
rs46006532	snp	G/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77498323	ACCTCCAACACCAAG[G/T]GAGGAACCACAGAGT	78514
rs46012229	snp	A/G	0.244898	0.249948	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485822	CAGTTGGGAAAAGCA[A/G]GTGCCAAGCACTATG	78514
rs46020806	snp	A/G	0.396694	0.202437	intron-variant	Arhgap10	Mm_Celera	8:77478436	CCCTGGTTTGAGATC[A/G]TAGAGGTTCGTGGAG	78514
rs46029904	snp	G/T	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77506839	CTGACCCTGACTTTG[G/T]ATACTAGGCAGCCCA	78514
rs46030322	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77370910	GGCGGAACTAAGGAG[A/G]GGTGGGACTTCCGAT	78514
rs46035397	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77300441	CTCTTCCATTGCTGG[G/T]GGGATTGCAAGCTGA	78514
rs46047732	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77313815	TCCAGGCCAGAGATC[A/G]TATCGCCCAGCAACT	78514
rs46049156	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77374857	CTACTGCAGCTGAGG[C/T]TCACATGCAGACAGT	78514
rs46053856	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77457064	GATCAAGGTATGGAC[A/G]CTTTGCCCCTTCTTG	78514
rs46062579	snp	G/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77402976	TAACATGCCCAACTC[G/T]TTCAGTCTGAAGAAC	78514
rs46064788	snp	C/G	0.408163	0.193609	intron-variant	Arhgap10	Mm_Celera	8:77474704	GCGGGTAAAGCGCTT[C/G]GTAACAGTCACAGTT	78514
rs46067862	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77416783	CTGATCAGGCCTTAA[A/G]ACTCCAAAACACAGC	78514
rs46088866	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77496453	AGCAGGCTCTCATTC[A/G]CCTGTCCTCAGCTTA	78514
rs46092956	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77496271	AAAAAGAATTAAAGG[A/G]CCACTGCAAAGAAGC	78514
rs46099905	snp	C/T	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77413153	CCTCCAGCACCTTCC[C/T]TAATAACAGACATAG	78514
rs46100836	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77454190	GCATCCTGACAGCCC[A/G]GTGAAGAGGCAAACG	78514
rs46103966	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77457058	AACAAAGATCAAGGT[A/G]TGGACACTTTGCCCC	78514
rs46106918	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77498721	CCTCAATCAGGTTAC[A/G]GAAAATCAGCTCTGA	78514
rs46114231	snp	G/T	0.489796	0.070696	intron-variant	Arhgap10	Mm_Celera	8:77406838	ACCAAACTGAGAACA[G/T]ACAAGTGGGCGGAGG	78514
rs46122137	snp	C/T	0.495868	0.0452663	intron-variant	Arhgap10	Mm_Celera	8:77396343	AAAACTGCAGAAGGG[C/T]GTCCATGCATTATAG	78514
rs46133347	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77433097	TCCATAAACAACAAA[A/G]GGCTCTGTCATACCC	78514
rs46136466	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77436414	CAAGAGACCCGGCTG[A/G]ATGCCATTCTACCAC	78514
rs46141579	snp	A/C	0.297521	0.245442	intron-variant	Arhgap10	Mm_Celera	8:77506505	GTCAAAGCCACAAAA[A/C]TTCTTTTACAAATTC	78514
rs46158746	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77378412	GGCTTAGCAGGAGGT[C/T]CCTAGGCCAGCCCTA	78514
rs46164761	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77404291	GCACTGGTGTGCAAG[C/T]GTGGGCAGCCTCTGA	78514
rs46179451	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77374376	AGCTAAGATCGGTCC[C/T]GGCCCATTCAGCTGC	78514
rs46180464	snp	C/T	0.142012	0.225474	intron-variant	Arhgap10	Mm_Celera	8:77496061	CCTAGTATCTTCATG[C/T]ACCCTACCACCATGT	78514
rs46189220	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77398707	TTCCCAAAACCTAGT[A/G]TAAATTCATCTTATA	78514
rs46190728	snp	C/G	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77404577	GAGAAGCTCTTAACT[C/G]CTATTTTAGACCAAA	78514
rs46193188	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77451362	TCCAGTCCAAGCCAA[C/G]CAAGGAAACCAGAAA	78514
rs46197615	snp	A/G	0.408163	0.193609	intron-variant	Arhgap10	Mm_Celera	8:77400935	ACAGTGCGGATCTGC[A/G]TCCTCACCCCTCACC	78514
rs46212016	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77467585	CAGCACCTCCATGGA[C/T]CAGATACCATGCACG	78514
rs46213263	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77405714	CCAAAAGCAATAGGC[A/G]TCTATAATCCAAAAA	78514
rs46213311	snp	G/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77479828	GGCCTTTCAAGTCAC[G/T]GTGCAAGTGTGCGCT	78514
rs46213777	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77459186	ATAGTTCTTATTTTC[A/G]TTAAAGTTCTCATTT	78514
rs46217702	snp	A/C	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77396711	TCACTGGCTGAACTG[A/C]GGACATGACTGATCT	78514
rs46230299	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77498665	CCTATGAAAGCCCCG[C/T]CAACTATGCAGAGCA	78514
rs46233677	snp	C/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77504278	TGTACAGTCTGGGGG[C/G]GGGGGGGGAGCAAAA	78514
rs46233886	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77500389	GATGTGTTATTCTAA[A/G]TGGAGATATACATCC	78514
rs46263897	snp	G/T	0.152778	0.230321	intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77492718	TTTATAGAATACATA[G/T]TTTCTCCTAGAAGAC	78514
rs46269149	snp	A/T	0.152778	0.230321	intron-variant	Arhgap10	Mm_Celera	8:77469829	GCTACCGAAGTTGAA[A/T]ATGATTCCACCAGGC	78514
rs46279667	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77370969	TAACAAACAAGCAGA[C/T]ACTAACAAAGAGAAA	78514
rs46284603	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77428052	AATGGCAAGGAGCAA[A/T]TGTTTCTTATGAAGC	78514
rs46286928	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77435672	AAAGTTACCCCAGGA[A/G]CCCTGAGATCCTAAT	78514
rs46293367	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77352947	CCCCACCTCCCTCAC[C/T]CAAGTACATGTCCTT	78514
rs46296202	snp	A/T	0.486111	0.0821678	intron-variant	Arhgap10	GRCm38.p3	8:77459146	AATATAGGCTTTGAA[A/T]GCTGGGGTCCCACAA	78514
rs46300316	snp	A/G	0.408163	0.193609	intron-variant	Arhgap10	Mm_Celera	8:77405308	GGGTTTCAGAGTTAC[A/G]GATCTCAATGTACAT	78514
rs46302451	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77456058	AGAAGCTTGCACTCC[A/T]TGGCATAAAGGCCTA	78514
rs46311735	snp	A/G	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77418647	CTGTTCTCATTTTAC[A/G]CGAGTCCCATAATAC	78514
rs46319407	snp	A/C/G			intron-variant	Arhgap10	GRCm38.p3	8:77374850	GTTGTCCCTACTGCA[A/C/G]CTGAGGCTCACATGC	78514
rs46328697	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77410036	TCACAGCTATACTCT[A/G]CACTGCTTCATTTGG	78514
rs46355669	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77408621	TCCCTGAGTAGCGCA[A/G]ACCAGAGTCTTAGGA	78514
rs46364820	snp	A/C/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77405062	TGAGGAGCATTCAAC[A/C/G]CTGGCTAATACGGCA	78514
rs46368397	snp	A/C	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77404559	AGAAATACCACAACT[A/C]CAGAGAAGCTCTTAA	78514
rs46370258	snp	C/T	0.152778	0.230321	intron-variant	Arhgap10	Mm_Celera	8:77512192	GATGGGACAGACCAA[C/T]AATGGTTCATAAAGA	78514
rs46372581	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77267294	CCTCGTGAACCTCCC[C/T]CTTTAAGAGAAAGGC	78514
rs46387212	snp	A/G	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77408697	CGCATTCTTTCTCCC[A/G]CGATCTTGGCAAACG	78514
rs46390712	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77328635	CTACCAGAGCACATC[C/T]GCACCGCCCATACCG	78514
rs46397482	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77374811	TTGTTCCTACTGCAA[C/T]TGAGGTTCACATGCA	78514
rs46401771	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77504620	CATTTCAGAGGATCC[A/G]TCATCACGGGGCGAG	78514
rs46405436	snp	G/T	0.231111	0.249285	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77502804	TGTCTGGAGACTTGC[G/T]CCCACGGCCCAGCAG	78514
rs46422166	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77454239	CTGTTGGCGGGTGGC[A/G]GCACTGCTGAGAATC	78514
rs46434004	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77286751	TATCTTCTTATAGCA[C/G]ATGAAAATTGCAAGA	78514
rs46434291	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77457076	GACACTTTGCCCCTT[C/T]TTGGAATTGGGAGCA	78514
rs46439178	snp	A/C	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77496454	GCAGGCTCTCATTCG[A/C]CTGTCCTCAGCTTAA	78514
rs46443557	snp	A/G	0.197531	0.244432	intron-variant	Arhgap10	Mm_Celera	8:77477821	AGATAAACAATTCTT[A/G]GAAAAATAGCTCGTC	78514
rs46452955	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77427540	ACAGCATCTCTGTGC[A/G]TTTACATCCATTACA	78514
rs46454085	snp	C/G	0.32	0.24	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493644	AAAGCAATGGAACCA[C/G]TGGTGATGGACTAAA	78514
rs46455375	snp	C/T	0.277778	0.248452	intron-variant	Arhgap10	Mm_Celera	8:77410868	TCTAACTGTGAAGAC[C/T]GAGGAGTGTGATTTA	78514
rs46464556	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77501116	AGACACACGCAGCAA[A/G]CTACAGCACAACTGT	78514
rs46466243	snp	C/T	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77486630	GCAAGCACCGTATTC[C/T]AAAATCCCAGTTATA	78514
rs46469749	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77419458	CTCACAGGCCAACTG[A/G]GCCCCTGAGAGTCCT	78514
rs46472276	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77328708	TGGGTAGCTTGGTCA[A/T]CAGCTGCTGCTCTAA	78514
rs46478480	snp	A/G	0.35503	0.226867	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493579	TCCGTCCCAGGCATG[A/G]AAGTTTGTTGGGCTA	78514
rs46481065	snp	A/G	0.277778	0.248452	intron-variant	Arhgap10	Mm_Celera	8:77506333	TGTTGGTTCTCCTGC[A/G]CCTTCCAGAGGCCAC	78514
rs46497562	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77397658	GTGGTGGTAACACGC[A/G]TGACAGGTTCTGCTT	78514
rs46502502	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77374445	CAGGAAAGCCTTGCC[A/C]CAGAGCCTTCTGATT	78514
rs46508680	snp	A/T	0.489796	0.070696	intron-variant	Arhgap10	Mm_Celera	8:77508370	TATTGTTAGCTTGAA[A/T]GAAAAAACAAGCCCA	78514
rs46520075	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77408212	CATACAGCATCATCA[A/G]TGTCTCCAAAAGTAG	78514
rs46529202	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77478564	TTGCCTTATACTTTA[C/T]TTCAGATCCTACCAA	78514
rs46532510	snp	A/G	0.165289	0.235211	intron-variant	Arhgap10	Mm_Celera	8:77508802	ATCAACTGAACCCAA[A/G]ACTTGGAGTCATTGT	78514
rs46536635	snp	C/T	0.152778	0.230321	intron-variant	Arhgap10	Mm_Celera	8:77467770	CTGCCAGCAGGTCCA[C/T]AGCAGACTGACCCTT	78514
rs46539112	snp	C/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77389146	ATTCCTATTATATAC[C/T]GTATCTCTACAAATC	78514
rs46541355	snp	G/T	0.132653	0.220748	intron-variant	Arhgap10	Mm_Celera	8:77410386	TGTGTGGCCAGTTAT[G/T]CTCACTCCTAGTGGG	78514
rs46544704	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77403009	AGCTGCACACACACA[C/T]AAAGACCTGCGTTGC	78514
rs46554593	snp	C/T	0.336735	0.234472	intron-variant	Arhgap10	GRCm38.p3	8:77456187	TATAGAAGAACAAGG[C/T]TCAGATTCTAAGAAC	78514
rs46560069	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77397697	ACCAATGCAAATGAC[A/G]ATAGTAATAAACTAG	78514
rs46566188	snp	A/G	0.408163	0.193609	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484561	ATGACTGATGGTTTT[A/G]GTAAGTATTTGTATC	78514
rs46573539	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77408331	ATCCAGCAAAGCAGA[C/T]TTCCGATTCATCTGT	78514
rs46576390	snp	C/T	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77467599	ATCAGATACCATGCA[C/T]GACCAACCCATCTTC	78514
rs46579465	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77298095	CTCTTGGCTCCTCTA[A/G]CACCATGTCTGCCTG	78514
rs46588006	snp	C/G	0.336735	0.234472	intron-variant	Arhgap10	GRCm38.p3	8:77402121	CCCCAACTGAGCACT[C/G]TTGCCTACAGTGTTT	78514
rs46591247	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77417763	CTATGGCGCGTGGCT[A/G]AAGTGGAGAAGGTGG	78514
rs46592803	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77374175	TCTATGCTGTACATA[C/T]CCTCATTTAAATCAC	78514
rs46598014	snp	A/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77470747	TCTGGGGAGTTATTC[A/T]TTTTTAAGATTTGTA	78514
rs46602500	snp	A/G	0.493827	0.0552116	intron-variant	Arhgap10	GRCm38.p3	8:77444927	TACTGCAGAATTACT[A/G]AGCGCACAGGCTTTT	78514
rs46608122	snp	A/G	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77409148	TGGAAGGGTTTGCCT[A/G]TGATCGCCAACCTCA	78514
rs46615139	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77455784	GCCATGGTAAGCAAG[C/T]CAGTAAGCAGTACCC	78514
rs46616109	snp	C/G	0.336735	0.234472	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484843	AGAGAAAATTACAGG[C/G]AGCTCTGTCTACAAC	78514
rs46616498	snp	C/T	0.142012	0.225474	intron-variant	Arhgap10	Mm_Celera	8:77460681	TGTAACTTGTGATTG[C/T]TCCCCTTGCTCCCAC	78514
rs46642537	snp	A/C	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77472795	CAAGGAAAGCTGGGC[A/C]CTGTAGATCCCCAGT	78514
rs46650303	snp	C/T	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77409372	AGTCTTCAGCCAGGA[C/T]AGAGCTATGACCCTA	78514
rs46657413	snp	A/G	0.277778	0.248452	intron-variant	Arhgap10	Mm_Celera	8:77409889	GTCACCCTCCCTAAG[A/G]GCATTAGAACTGGGG	78514
rs46688353	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77483815	TGGTCTGTGATCTTC[C/T]GCTTCTTGGCTGCTG	78514
rs46691935	snp	G/T	0.231111	0.249285	intron-variant	Arhgap10	GRCm38.p3	8:77498502	GGGGAAACCCCTAGA[G/T]AAGAGTCTGTACCTT	78514
rs46693962	snp	C/T	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77407559	CACTAACAGCCAAGG[C/T]GAGGAAGGCTGGGAG	78514
rs46705293	snp	C/T	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77415843	CAGTTTGCTTTGCCA[C/T]ACATGATGACTGTGG	78514
rs46709860	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77458395	TCCCTCAGAATCCTA[C/T]TCAGTTTCCAAGGGT	78514
rs46714353	snp	C/T	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77470701	TGTAAGTTCATCTCC[C/T]AGAAGAGACATTATT	78514
rs46714809	snp	A/G	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77412171	GAAGAGTCGGAGGCT[A/G]AACCACGATCCTAAC	78514
rs46716580	snp	A/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77314406	CCCAGGTCTCTTTCT[A/G/T]GGTGCTTGGCTCCCT	78514
rs46716770	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77458440	ACTGGAAGACCCTCA[C/T]ACTGCAAGGTGCTCC	78514
rs46722398	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77252199	CCCCATAAAGACCAG[A/T]TGAGGGACCTCATGC	78514
rs46728356	snp	A/G	0.244898	0.249948	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493855	TTCTATCGAGGGTAC[A/G]TCACTTTGACTTATA	78514
rs46730197	snp	A/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77468082	GGACATGAGACCCTT[A/T]CTGAGATTTCACCTA	78514
rs46735473	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77254300	GTCTGATAGTACGAA[A/G]AGAAAGAGCAGGCTG	78514
rs46736380	snp	G/T	0.35503	0.226867	intron-variant	Arhgap10	Mm_Celera	8:77472908	CCTCATCTCTACAGG[G/T]GTGCTGCGGCAGGGG	78514
rs46736686	snp	C/T	0.165289	0.235211	intron-variant	Arhgap10	GRCm38.p3	8:77505837	GCAACTCAGTATCTC[C/T]GAGCAGTCATAATCT	78514
rs46751533	snp	A/G	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77495676	TGACAGCAGTCTTCA[A/G]GGTTTGGGGACAGTG	78514
rs46752794	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77422144	TCATGGAGGCACTAC[C/T]GTTGGAGGGATTAAG	78514
rs46762974	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77274571	TTAAGAAAAGAAAAA[C/T]GCAATCAGTCCAGGT	78514
rs46776665	snp	A/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77486114	ACATACAGAAAAGGG[A/T]CTGCTGCAAACTGGA	78514
rs46776747	snp	C/T	0.142012	0.225474	intron-variant	Arhgap10	Mm_Celera	8:77458271	TTGACCTGTTTTCAC[C/T]GCTGCTCTAGGACTC	78514
rs46787733	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77314132	GCATCAATTCAGACA[C/T]AGCCACCTCAGTGTA	78514
rs46792070	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77353081	CTCTCAATTTAAAAA[A/T]GTTCAAGTCAAAGGC	78514
rs46792537	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77388995	GAATTCAATCTATTC[C/T]TGTCCCCATCACCTG	78514
rs46796079	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77254898	CTCCACAGGCCCTAC[A/G]ACCTGCCAACTATTT	78514
rs46797418	snp	C/T	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77405679	TAGATGCTCTCTAAC[C/T]GAGAAATGAAGAAAT	78514
rs46799090	snp	A/G	0.5	0	intron-variant	Arhgap10	GRCm38.p3	8:77460572	ACCTTGCAGGAGCAA[A/G]GGCACAGGTGCACCT	78514
rs46811895	snp	A/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77500012	ACGCAGCTCTACGGT[A/T]GATGTGTGTCGACTG	78514
rs46812854	snp	A/T	0.32	0.24	intron-variant	Arhgap10	GRCm38.p3	8:77457850	ACTGGTTCTTTTGTT[A/T]AAAAAGTTCTAGTAA	78514
rs46815238	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77424748	CAGTTTTATGCTTTT[A/G]TTGGGAAGTCATAAT	78514
rs46819212	snp	C/G	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77496747	CACTAGGTTCATAAT[C/G]GGACTAAATGTTTGT	78514
rs46819986	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77324396	TTAGTCAGAAAAGAA[A/G]GACTGACAGGCATAA	78514

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