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
rs46820745	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77448196	ACACACACACAAACA[C/T]ACTCCTTATATAATA	78514
rs46827833	snp	C/G	0.132653	0.220748	intron-variant	Arhgap10	Mm_Celera	8:77458298	ACTCCTTAAGAACGA[C/G]TGGAACTGTGTTTGG	78514
rs46830385	snp	G/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77513194	TCGAGTTTAAGAGAT[G/T]TGTGCTTCTTAGTTT	78514
rs46851808	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77472342	AAGTAATATGACAGG[C/T]CATGGTGATTATGGC	78514
rs46861896	snp	C/T	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77410672	CTGAATGAAAGGGGA[C/T]TGATTCACTCAAAGG	78514
rs46872354	snp	A/G	0.142012	0.225474	intron-variant	Arhgap10	Mm_Celera	8:77473160	GGTCGACAAGAAACG[A/G]CTCAGCAGGGAGAGC	78514
rs46878469	snp	C/T	0.124444	0.216185	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494522	CATCACCCAAAAATG[C/T]ACTGTTTAACTCCAT	78514
rs46879773	snp	A/T	0.336735	0.234472	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485710	CTGCATCAAGTCCAT[A/T]GTCAGAAAAAAAGAG	78514
rs46881847	snp	A/T	0.32	0.24	intron-variant	Arhgap10	GRCm38.p3	8:77489016	GCTCACTTCTTAGTT[A/T]ATTTGTAGCCACAAA	78514
rs46887478	snp	A/T	0.336735	0.234472	intron-variant	Arhgap10	GRCm38.p3	8:77489448	GCCATTGAGGAACTT[A/T]GTAAATAACAAATGC	78514
rs46891775	snp	A/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77404618	GGCTCACGAAGCCTC[A/T]CCTGCAATGCCACTT	78514
rs46892717	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77320057	AGTAATTGGATACTA[C/T]AAATGAGACAGAAAT	78514
rs46902104	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77254892	GCCTGGCTCCACAGG[C/T]CCTACGACCTGCCAA	78514
rs46906550	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77256633	TCCAGCATCCAAGGT[G/T]TCCCTGCTTCCTAGG	78514
rs46920208	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77275684	CCAACCCCGCCCCCA[C/T]CCAGCTAGAAAGTCA	78514
rs46921405	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77369083	AGAAGCACATACTAG[A/T]CAATTTTTGTTTGTT	78514
rs46921528	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77271722	ACTTTTTCTTCTGTG[C/G]AGGGAGCCTAAAAGG	78514
rs46936442	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77281664	ACAGCTGATAATAAA[C/T]AGAGCAAAAGGTGGC	78514
rs46940082	snp	A/G	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77405958	CACAAAAAAGCAGGA[A/G]CTCTGAAAATGACTT	78514
rs46961497	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77505529	CTTTAATCCCAGCAC[A/G]TAGGAGGCAGAGACA	78514
rs46961962	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77403787	TGCACGATGCAGGTT[A/G]TCTTATGCTTTCAGG	78514
rs46966862	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77448777	CACTGCCGCATCCCT[A/G]GCCCTGTGCACACTG	78514
rs46990846	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77410088	AGCTATCGCTAAGGA[A/G]AACTGCCCTAAAACC	78514
rs47008177	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77507132	GCACGCTTGTAAAAA[G/T]CCAGGTGTGGTCCCC	78514
rs47012006	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77372182	GGGGAAATGCTTGGA[C/T]AGAGACCAAAGCAAA	78514
rs47023101	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77371809	CTTCTTGACATTCTC[C/T]GCCCAAACCAACAAG	78514
rs47044568	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77254268	CCAAGAACTGGAATT[C/T]GTAGCCCAAGTCCAT	78514
rs47076710	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77252304	ACTTGTGTTCCCTGG[C/T]ACCTAGCCCAGTGTC	78514
rs47078669	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77319997	CATGAAAACAAGACT[A/C]ATTAGTTGAAAATCG	78514
rs47095258	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77271877	CACGAACTCCGAGGA[G/T]CCTGGGCTAGCAACT	78514
rs47099398	snp	A/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77469879	TCTCTGACTGTAAAG[A/T]GCCCAGGAAGACGTT	78514
rs47102780	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77497514	TTTAGAAACTGGTAG[A/G]TTTAAACAAAGCTCA	78514
rs47103817	snp	C/T	0.35503	0.226867	intron-variant	Arhgap10	Mm_Celera	8:77467169	ATTTCTGTTGTACGG[C/T]ACTAGTACAGTTTCA	78514
rs47106132	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77424386	AGGCTGAGGCAACAG[A/C]CTGGAGCATCAGGTA	78514
rs47107969	snp	A/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77404732	GAAATTGCCATTCAA[A/T]AAAGACCTCAACAGG	78514
rs47128780	snp	A/G	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77500255	CTCATACAGCAGGTG[A/G]AGATAATGCTCAGTA	78514
rs47133611	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77450650	CCAGACTGTCCCCTC[A/G]TGGAAATCTGGTAAT	78514
rs47139579	snp	A/G	0.297521	0.245442	intron-variant	Arhgap10	Mm_Celera	8:77508014	ACAGCAAACCCATCC[A/G]TCACATGACAAAGGT	78514
rs47139645	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77275896	CAGTGGCTAACTAAA[C/G]TTGACTTCACTGGCT	78514
rs47154750	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77514360	CTTCCTTATTATAAG[A/G]CATCGCTGAGCTCTG	78514
rs47158798	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77457022	TAAGATACAATTTGC[A/G]AAACACATGAAGCTC	78514
rs47166024	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77401351	GTTGTCAATGCTTTC[C/T]GCACAGAAACTAAGC	78514
rs47168298	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77253603	TTTCAGCTCTGAAAG[C/T]GCAACACAGGCCCCA	78514
rs47182256	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77275975	GCTCACAGACTAACT[C/T]CAACCCTAGTGCAGC	78514
rs47191688	snp	A/G	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77398359	GGCACTTCTAAAAGA[A/G]GCTGTTCAAAACTCC	78514
rs47197273	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77416802	CCAAAACACAGCAAA[C/T]GAGAATCTCTGGACT	78514
rs47204680	snp	A/C	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77488170	AAGAGAAGCTCCTGA[A/C]TGTAAAGGATGTACC	78514
rs47215650	snp	C/T	0.32	0.24	intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77492959	CTATGTGGACAACTA[C/T]GGGTTTAAACAATTG	78514
rs47237290	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77405074	AACGCTGGCTAATAC[A/G]GCACAAGTCTGGTGA	78514
rs47242374	snp	A/G	0.42	0.183303	intron-variant	Arhgap10	Mm_Celera	8:77478464	GAGACAAGGAAAGAA[A/G]CGTGTCAAACAGCCA	78514
rs47243420	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77498852	CTTTTTTTGAAAGTT[G/T]TTTGAGACAGTGTTT	78514
rs47251882	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77449685	CAGCTAGGTACCACC[C/T]GGGAGATCCAAAGCA	78514
rs47259843	snp	A/G	0.152778	0.230321	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493967	GGCCAAAATATAAAC[A/G]ACTGTGTCTAATCTG	78514
rs47274476	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	GRCm38.p3	8:77402191	CTCTGGGCTTTCCAA[C/T]TGTCATCTATTCTGC	78514
rs47282053	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77251634	AGTCGCATGACAAGG[C/T]CCAGACTGGACAGCA	78514
rs47286655	snp	A/T	0.132653	0.220748	intron-variant	Arhgap10	Mm_Celera	8:77463296	ACATGTGGTCTCAGT[A/T]GCTCTCAGAAGCCAA	78514
rs47298386	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77403071	TTCAGGAACACAGGG[C/T]ACTATGCCTGGTGGC	78514
rs47300267	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77403450	TCAAAGATGAGTGGC[A/G]TCAGCACGTGTCAGC	78514
rs47302153	snp	A/G	0.495868	0.0452663	intron-variant	Arhgap10	GRCm38.p3	8:77460488	AAATGTGGAGATGCC[A/G]GTCACACAGTGAGGT	78514
rs47310997	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77396784	TCCAATCATGCATCA[C/T]AGTGAGCCTTGCTAA	78514
rs47313216	snp	A/G	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77486321	GTTAGCATTACAGCT[A/G]TGAGCTACCCTGCCT	78514
rs47314261	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77314453	CTCCACTATTTTCTA[C/T]TCCTTAATTTAGCAC	78514
rs47321221	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77497870	TTAAGTTCGTGTTTA[A/G]AATGTAGCATGCTCA	78514
rs47323023	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77516670	CTTGGCTCCTGCACT[A/G]TCAGGCCTTTTAAGG	78514
rs47323742	snp	A/G	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77400349	CCTCAGCTACTTTCC[A/G]AGCTGTAACTTGAGA	78514
rs47337935	snp	A/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77372800	GTTCAGACCTAAGCC[A/G/T]CTCACTGGAGTGTGA	78514
rs47339024	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77314811	ATAGACTCCATCACT[C/T]GTGCCAGAGGTGAAG	78514
rs47343966	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77495733	AGCTACATGTTCTTC[A/G]TTAGGAAAACTTTGA	78514
rs47344206	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77401123	TATACATTAATTATA[A/G]TGGTTTTTCACTTTA	78514
rs47354384	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77378666	CCAGGCCTCCACGAA[A/T]AAGGATGCTCTAGAG	78514
rs47358880	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77427438	GCTCTTCACTGCGTC[A/G]CAGGCTCATCCCCTT	78514
rs47362228	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77314291	TCTTTTACTTTAAAT[C/T]GCCGAGCTGTTTTCT	78514
rs47363788	snp	C/T	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77404721	CAAGCAACTATGAAA[C/T]TGCCATTCAATAAAG	78514
rs47363841	snp	A/C	0.32	0.24	intron-variant, utr-variant-5-prime	Arhgap10	GRCm38.p3	8:77492334	TGATCTCATGCTTTA[A/C]AACATATCACTTCCA	78514
rs47371127	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77320622	CAGCTCATCCCCCTG[C/T]ACCACACCCCAGTTT	78514
rs47383696	snp	A/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77464450	TCTTGTGCAAGAAGG[A/T]CGATTTCATAAAGTC	78514
rs47402213	snp	C/T	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77410421	GCTCTACCCCAGACA[C/T]CAATGTTCACCTTAA	78514
rs47403577	snp	C/T	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77399983	TGAGACTACAGATTC[C/T]GCCATTACACAGGGT	78514
rs47410268	snp	G/T	0.46875	0.121031	intron-variant	Arhgap10	Mm_Celera	8:77508091	TCCCGCTCCCAGTGG[G/T]CCAGGCACAGCTGGC	78514
rs47427200	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77253604	TTCAGCTCTGAAAGT[A/G]CAACACAGGCCCCAT	78514
rs47432910	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77449954	CTGAGCCCCCTCACA[C/T]GTCAACCTAATCTAG	78514
rs47451099	snp	C/T	0.46281	0.131194	intron-variant	Arhgap10	GRCm38.p3	8:77457823	AGTGCTGAGTACAAA[C/T]AGCACCTGACCACTG	78514
rs47456159	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77275935	CATTCACTGAAGGAG[A/C]TAGGGATCTGGACTT	78514
rs47456332	snp	C/T	0.142012	0.225474	intron-variant	Arhgap10	Mm_Celera	8:77467732	TCTCTTCTAGGTAAC[C/T]CTGGGAGACTCATCT	78514
rs47458887	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77320654	TGTCCTACCTCCTGT[A/T]AAAGTCCCTAGACTA	78514
rs47462978	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77497576	ATCACTGCATGGTAT[A/G]TGTCCAAGACAGCAC	78514
rs47466846	snp	C/T	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77417736	GTAATGACGGTCCTT[C/T]CGAGGGAGAGCCTAT	78514
rs47494701	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77374369	GCCCAGCAGCTAAGA[C/T]CGGTCCTGGCCCATT	78514
rs47499066	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77417217	TCTAAAATATCCTTT[A/C]ATTTTGATACAATTT	78514
rs47501101	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77506221	TATAGATTACATGTT[A/C]TTCTAAGTTTTCTCC	78514
rs47504107	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77352872	TGAATCTCTCTGTCC[C/T]CATCGCTGACTGGAC	78514
rs47506640	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77417106	ACTCTTACCTACTTC[A/T]TCTATCACCTGGAGG	78514
rs47511597	snp	C/G	0.132653	0.220748	intron-variant	Arhgap10	Mm_Celera	8:77513181	AGCTAAGCAGGGCTC[C/G]AGTTTAAGAGATTTG	78514
rs47514760	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77498664	GCCTATGAAAGCCCC[A/G]CCAACTATGCAGAGC	78514
rs47517827	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77458820	TTGTGGTTTTGGCAT[A/G]ATTTCTGGAGGAGCA	78514
rs47521848	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77414309	CACCCAGCTTATGGG[C/T]ATTTCTTGCAGCCAG	78514
rs47521916	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77442102	TGTACTGATTACACA[C/T]ATTCCCCCATGCTCA	78514
rs47523103	snp	A/G	0.277778	0.248452	intron-variant	Arhgap10	Mm_Celera	8:77508781	AAGGAGACTAAAGCA[A/G]GGAGAATCAACTGAA	78514
rs47528684	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77251387	GGAGGCCTCTGCGCA[C/T]GCAGCACTTTACTTG	78514
rs47531870	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77403473	GTGTCAGCCCGTGGT[A/G]TTTGAATGAGACTGC	78514
rs47539198	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77378662	CCCTCCAGGCCTCCA[C/T]GAATAAGGATGCTCT	78514
rs47545455	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77457135	AGAGTTTGGAGCTGA[A/G]ATGAAAGGATGGACC	78514
rs47559811	snp	A/G	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77488087	CTACCAAGTCAAACC[A/G]GCCTGGGATCAATAC	78514
rs47562562	snp	C/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77468094	CTTTCTGAGATTTCA[C/G]CTACTCAGTTTCCTC	78514
rs47571848	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77498676	CCCGCCAACTATGCA[C/G]AGCAACCAGGTAGGG	78514
rs47579414	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77404841	GTCCTGGAACTCACT[C/T]TGTAGACCAGGCTGG	78514
rs47579468	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77255464	GAAGTCCTCTATATC[G/T]CGCTAATACATCCTT	78514
rs47614861	snp	A/G	0.260355	0.249785	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493752	CTATCTGCCGAACAG[A/G]AGGGGCTCGGAAGCA	78514
rs47616830	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77400712	AGCCCCGTAACATTC[C/T]TATCAATCAACTGTG	78514
rs47621554	snp	A/G	0.244898	0.249948	intron-variant, utr-variant-5-prime	Arhgap10	GRCm38.p3	8:77492321	AGCCCAAAAGACCTG[A/G]TCTCATGCTTTAAAA	78514
rs47622107	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77422112	GGAATCTTCAAGAAA[C/T]GAGGCCTGCTCCGGG	78514
rs47627818	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77464409	AAGTAGAATGAGAAG[A/G]GCAAAGGCAGCCAGT	78514
rs47627942	snp	C/T	0.336735	0.234472	synonymous-codon	Arhgap10	GRCm38.p3	8:77413616	TCTGGTTCCCTCAAA[C/T]CGATTCCGTGTCTGA	78514
rs47631380	snp	C/G	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77479366	CTTCCATCTTGGTTA[C/G]TGCCTGAGGAGGTAA	78514
rs47631529	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77353033	AAATTGAGTCTCTAA[A/G]AGAAACCATATTCTG	78514
rs47639135	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77253487	ATTTCTGCAAAGCTG[C/T]AAGCACAGCAGAATC	78514
rs47648579	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77374171	CATCTCTATGCTGTA[A/C]ATACCCTCATTTAAA	78514
rs47657182	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77252135	TAAATATTGGACACT[C/G]CAACCATGCCTGGGC	78514
rs47660052	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77298777	GTGACCCTAAAAATT[A/C]TACCAGAGAACTCCT	78514
rs47660071	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77404236	ACACACAGATGCAAC[A/G]TTCCAGCCTCAAGAT	78514
rs47665839	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77458184	GGTGCACGAAGGACA[C/T]TTTCTAAAGGTTCAA	78514
rs47681562	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77377002	AAATCAAGGTCTGTC[A/T]TGTCTTTTCTATCCC	78514
rs47691068	snp	C/T	0.426035	0.177515	intron-variant	Arhgap10	Mm_Celera	8:77495993	AAGTCTATGAAATAT[C/T]TAAAAGTCATTCTGA	78514
rs47703072	snp	C/T	0.336735	0.234472	intron-variant	Arhgap10	GRCm38.p3	8:77490206	AATGCATAAAGCAAG[C/T]CATTCTACCAAGGGG	78514
rs47715887	snp	C/T	0.345679	0.230967	intron-variant	Arhgap10	Mm_Celera	8:77510468	AAAACTTTTAGAAAA[C/T]CATAGGCAAAGTTAG	78514
rs47725545	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77505701	GAGACACAGTATGTG[C/T]TTGGAGATGCAGACA	78514
rs47727629	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77416985	CCCCAGTGTCACAGA[G/T]GTTAGGACAGCTGTC	78514
rs47741490	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77375019	CCATCCTAATCCTCC[A/G]GTATCTTTCCTATAG	78514
rs47744880	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77277966	AAAAGATCCCAGATC[C/T]AAGCCACTAACAAAG	78514
rs47746363	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77455921	CTATCTCCCCAAATT[A/G]TTTTATCCATAGTGT	78514
rs47757860	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77467332	CATTTGCATCAATAA[C/T]ACCACAAAAAGCCGG	78514
rs47761547	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77396605	ACAGCAGACACTCAT[A/G]AAGAAGCTCTGTTGA	78514
rs47768864	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77425075	GGAACTCCAGCTCCA[C/G]AGGATTCACCACTCT	78514
rs47772008	snp	C/T	0.152778	0.230321	intron-variant	Arhgap10	Mm_Celera	8:77399865	CTGTTCTGGGTGTTA[C/T]TCTCTGCATGACATG	78514
rs47772171	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77396434	CTAGCAACAGCAAAC[A/G]GCAATTCTTTACCTG	78514
rs47772619	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77427312	TATCCCAGCTTCTGC[C/G]TGCAGAGATGACAGA	78514
rs47779531	snp	C/T	0.495868	0.0452663	intron-variant	Arhgap10	GRCm38.p3	8:77457745	ACCATCCAATCTCCC[C/T]TAAGCCACGTGCCAT	78514
rs47780044	snp	A/C	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77408160	GGAGAGAAAGGCTGC[A/C]GCTTACAATCATGTA	78514
rs47782894	snp	C/T	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77388020	GCCTTTACTGAATCC[C/T]GAACCCCATACGAGA	78514
rs47786789	snp	C/G	0.42	0.183303	intron-variant	Arhgap10	GRCm38.p3	8:77460291	ACAAACACTGCTCAG[C/G]CCACACTCAGCCTCC	78514
rs47787177	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77374594	CTTGGGTTTTCTCCC[A/G]TATCACAGCCCACGC	78514
rs47799980	snp	A/C/G			intron-variant	Arhgap10	Mm_Celera	8:77451403	AACATGTTCACTGAA[A/C/G]GTAGCACTACAGAGG	78514
rs47801170	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77406330	AGGAAAAACACATCG[A/G]GCCACCTCCAACATA	78514
rs47810297	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77507288	ATAATCAGGATAGCC[G/T]GATGGTCTCCTCACC	78514
rs47811021	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77251876	TACACCCCTGGTGAA[G/T]CAGTGTTTCCTTCCG	78514
rs47816352	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77403377	GTCTTAAGTTACATG[C/T]CCTGATAGACCATGG	78514
rs47832548	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77256035	CGAGTCACCAGCTGA[G/T]AAAATTTACCAAACA	78514
rs47835720	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77512510	AAAAAAAAAAGAGGC[A/C]TATTTTTTTTCTATC	78514
rs47839310	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77458190	CGAAGGACACTTTCT[A/G]AAGGTTCAAGGGTTC	78514
rs47848760	snp	A/G	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77398510	TCTTCCTGTCTGAAT[A/G]AACTGGTATAGTAGT	78514
rs47849129	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77380841	AGAAACCAAAGACCA[A/G]GGTGGGAATGACAGG	78514
rs47851363	snp	A/G	0.396694	0.202437	intron-variant	Arhgap10	Mm_Celera	8:77464980	CAGGTACGTAAGATT[A/G]CAAGAATACAGGAAA	78514
rs47853279	snp	C/G	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77413261	TTACCTCTAACCTCA[C/G]TTTCCTCAGAAACAA	78514
rs47854953	snp	C/T	0.35503	0.226867	intron-variant	Arhgap10	Mm_Celera	8:77513937	GGTTATTCTACAGAG[C/T]GCGGAGGAACGACAA	78514
rs47855886	snp	A/C/T			intron-variant	Arhgap10	GRCm38.p3	8:77436534	ATGGCAACGTTAGTG[A/C/T]GTTAGTTAGTAACTA	78514
rs47857526	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77254216	CTTGTGGTAGTGCAT[C/G]GCAGCAGCCCCCAGA	78514
rs47867732	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77352866	CAGATTTGAATCTCT[C/G]TGTCCCCATCGCTGA	78514
rs47871861	snp	A/G	0.495868	0.0452663	intron-variant	Arhgap10	GRCm38.p3	8:77461018	TCTACATCAGCCTAC[A/G]CCCCTCACCAACATC	78514
rs47874060	snp	G/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77412886	CTTTTTTATACGACA[G/T]CCAGGTCTCAAGTGC	78514
rs47885100	snp	A/G	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77456161	GAATCTAAAGTCACC[A/G]ATGATTTATTTATAG	78514
rs47896000	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77507081	TGGGCAGAGTGCTTG[C/T]TATACGATCATGAGA	78514
rs47896545	snp	A/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77401254	AAAGAATTCATAGCC[A/T]CAGTGTCCAAACCTA	78514
rs47909091	snp	A/G	0.124444	0.216185	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494960	AAGGGAATCCTTGAT[A/G]TGTCCATCATCTTTA	78514
rs47917119	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77450768	ATCTGTAAGGAGAAA[A/G]GCATGAGTCCATGCT	78514
rs47923816	snp	C/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77498741	ATCAGCTCTGAAGGA[C/G]AAAAGCCAGCTCCCC	78514
rs47925228	snp	A/G	0.132653	0.220748	intron-variant	Arhgap10	GRCm38.p3	8:77456295	TCTTCTAGGACTATG[A/G]ACTGGCCTCAAACAT	78514
rs47927024	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77342364	GTGTCCAGCCACAGA[A/G]GGGCAGAGAAAAACC	78514
rs47930271	snp	C/T	0.152778	0.230321	intron-variant	Arhgap10	Mm_Celera	8:77457776	CCACATGCATTATAC[C/T]CACTGCTCAGAGGTA	78514
rs47935358	snp	A/G	0.32	0.24	intron-variant	Arhgap10	GRCm38.p3	8:77489427	CATGAAAACCACCAA[A/G]TAAGTGCCATTGAGG	78514
rs47938629	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77500142	ATCTTTACATCCTAC[A/G]TGAAAATTCACAAGC	78514
rs47962066	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77378336	AGGAGCCTTGGGAGG[A/C]CAGAAGCAGAATGCC	78514
rs47962978	snp	A/C	0.244898	0.249948	intron-variant	Arhgap10	GRCm38.p3	8:77402245	GGAGCACTCAATGAG[A/C]TATCTTATGTGTAGC	78514
rs47993744	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77441296	ACACTAATGCAGCAG[C/T]GAAGTCCACAACCCA	78514
rs48005004	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77374565	CTATTAGAAGAGATT[G/T]GAAACCTAAATGTCT	78514
rs48010605	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77314565	CACTCCACAGCATAA[G/T]AAAAATCCAGACCAA	78514
rs48011867	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503820	ATGTGCTGAAGCAAA[C/T]CAAAGATTCCACCCA	78514
rs48018378	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77255052	AGTAAGGAAAGAATG[C/T]ACCCTGCATTGACAC	78514
rs48018931	snp	A/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77514856	CTTGTATCGTTTCAT[A/T]TCCTTTATTTCAAGA	78514
rs48022158	snp	A/G	0.5	0	intron-variant	Arhgap10	GRCm38.p3	8:77452208	AACACCTCATGACTG[A/G]GAAAGAAGAAGGCTC	78514
rs48027134	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77254296	CATGGTCTGATAGTA[A/C]GAAGAGAAAGAGCAG	78514
rs48033514	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77387854	TCCTTGCTGACTGTA[C/T]AGAACTCCTCTTCCA	78514
rs48061996	snp	A/G	0.277778	0.248452	intron-variant	Arhgap10	Mm_Celera	8:77450037	TGGGATACTGAACTC[A/G]GTGTCTTCTGCAAGC	78514
rs48066899	snp	C/G	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77505300	ACCCATGGCTTCACA[C/G]AAAATAATACCTCAA	78514
rs48068034	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77253859	CCCCATACCATCAAC[C/T]TCCCAGAGGATGCCA	78514
rs48069492	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77505947	TCACACCCAGTTTGT[G/T]TTCACCAAGCTGAAT	78514
rs48076035	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77369255	CCACCACACCCGGTC[A/T]TACTAGACAATTATG	78514
rs48077766	snp	C/T	0.345679	0.230967	intron-variant	Arhgap10	Mm_Celera	8:77480860	GTTCTTCCTAGTAAC[C/T]GGACTTAATTTTATT	78514
rs48081487	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77314584	AATCCAGACCAAAAA[A/C]TCTTTTAACAATAAA	78514
rs48083850	snp	G/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77407606	AAGAATGTGCTTACA[G/T]CCTACACAGCAGCAC	78514
rs48102588	snp	A/G			downstream-variant-500B	Arhgap10	Mm_Celera	8:77249927	GACTGGGCCATGCCT[A/G]GGCCTGGAGTTTGCA	78514
rs48111244	snp	A/T	0.336735	0.234472	intron-variant	Arhgap10	GRCm38.p3	8:77489650	GGTTAAAAGTAACTA[A/T]CTCTGAATGTTTCCG	78514
rs48136495	snp	C/T	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77415581	CTCGTGCCTTTGCAC[C/T]AGAATAAGCAGGGTT	78514
rs48145784	snp	C/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77401073	AAATAAACAAGCCTG[C/T]TATCATTCACAGTGC	78514
rs48148525	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77372861	AATCAATCGCATCCG[C/T]CCTTCCACCCGAGTC	78514
rs48154209	snp	A/G	0.486111	0.0821678	intron-variant	Arhgap10	GRCm38.p3	8:77458589	AAGGCTTACAGTGGA[A/G]GAGGCTGAAAAGCTT	78514
rs48186452	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77410188	GCTTGCCTCAGCCTC[A/G]TCTGGGTGGCTGTTT	78514
rs48199067	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77372851	TGGTCTCCTCAATCA[A/G]TCGCATCCGCCCTTC	78514
rs48199963	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77374421	GTCACACAAGCCACC[C/T]ACCACAGCCAGGAAA	78514
rs48207024	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77410030	AGAACATCACAGCTA[C/T]ACTCTACACTGCTTC	78514
rs48213636	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77444012	TAATACATAAAGGTG[A/G]AGAGGTTGCCCTGCC	78514
rs48225224	snp	A/C	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77467512	AAAAAAATATTAAGA[A/C]CATCACAGAGGTCCA	78514
rs48228453	snp	C/T	0.142012	0.225474	intron-variant	Arhgap10	Mm_Celera	8:77514413	CTACCACAAACTTGT[C/T]GCTGAGAAGGTCGGG	78514
rs48236579	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77509733	GACATTCTATAGAAT[A/G]TCCACTGTACACTTG	78514
rs48241659	snp	C/T			downstream-variant-500B	Arhgap10	Mm_Celera	8:77250023	CCCAAAGCCCAGCTT[C/T]ATCAAGATGGGCAAA	78514
rs48270599	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77506061	AGGGTGATCTTGAAC[G/T]TGTGACCACCACCCC	78514
rs48277657	snp	G/T	0.197531	0.244432	intron-variant	Arhgap10	Mm_Celera	8:77508357	CTGGACTTTAAAATA[G/T]TGTTAGCTTGAATGA	78514
rs48281759	snp	C/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77509765	AGATAATGAGGATTT[C/T]CCACTGTAGCATTCC	78514
rs48287405	snp	C/T	0.277778	0.248452	intron-variant	Arhgap10	Mm_Celera	8:77507434	CTCCAAATTCCTCTG[C/T]TCGTTCATTCGTTCA	78514
rs48290746	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77448881	CACTGCCACATCCCT[A/G]GCCCTGTGCACACTG	78514
rs48292350	snp	A/C	0.231111	0.249285	intron-variant	Arhgap10	GRCm38.p3	8:77402206	CTGTCATCTATTCTG[A/C]AAAACTCAAGTTTAG	78514
rs48293081	snp	A/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77468243	TGGGGAAGCTGTTGT[A/T]CATCTTGCACTGACA	78514
rs48298733	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77347009	AATGGTGCTGGGAGG[A/G]TCCAGATTCACGGGG	78514
rs48305529	snp	C/G	0.48	0.0979796	intron-variant	Arhgap10	Mm_Celera	8:77403358	CAGGGGTGGTGCTGT[C/G]AATGTCTTAAGTTAC	78514
rs48307185	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77409984	ATGGGGATCTGTTAA[A/C]AATACTTTATAAGAT	78514
rs48314646	snp	C/T	0.18	0.24	intron-variant	Arhgap10	Mm_Celera	8:77507481	TACTCTTTTCCTTCA[C/T]ACTAAACACCAAACT	78514
rs48315639	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77478173	ATAAGTACCTCAGGA[C/T]TCATTTTCTCATTCT	78514
rs48322115	snp	C/G	0.396694	0.202437	intron-variant	Arhgap10	Mm_Celera	8:77483039	CATATCATGCCCACT[C/G]TGAGTAGCAGCCCAG	78514
rs48326760	snp	A/C	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77401832	CTCAATAGTAACTGA[A/C]CAGTATATTGAACAG	78514
rs48328359	snp	A/G	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77405007	ACAAAGGTGCTGCCT[A/G]ATGGGCCCTGGCCCA	78514
rs48332508	snp	A/G	0.35503	0.226867	intron-variant	Arhgap10	GRCm38.p3	8:77488627	TACATGCAAAGTGCT[A/G]GGCTATGCAAAGACC	78514
rs48335652	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77251996	TCTTCTTACTGAGGC[A/C]ACCATTTGTTTTCCC	78514
rs48351421	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77372086	TGGCTGCCCTTACTT[C/T]CCATTCATACAAAAC	78514
rs48364572	snp	C/T	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77458535	CAGATTCTCACCAAC[C/T]TGCTCAAAATCATAC	78514
rs48365957	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77425151	TACACTGGCATTCAT[A/G]TGTACAGATTCCCCC	78514
rs48366433	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77254217	TTGTGGTAGTGCATG[A/G]CAGCAGCCCCCAGAC	78514
rs48382670	snp	C/T	0.35503	0.226867	intron-variant	Arhgap10	Mm_Celera	8:77514293	CTCACTCTTCCCGGG[C/T]TCTGCAAGTGTTCCG	78514
rs48384224	snp	A/G	0.495868	0.0452663	intron-variant	Arhgap10	GRCm38.p3	8:77460923	ATTCACAGAGAAGAC[A/G]CTGGGACAGCCAGCA	78514
rs48386348	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77252270	ACTACAACTCAAAGT[A/G]CAGAACATACATAAA	78514
rs48387448	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77274516	TAGAAGAGCATATTC[C/T]ACATACTGGCAACCA	78514
rs48388763	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77422092	ACGTCATTCTTGGGG[A/G]TGATGGAATCTTCAA	78514
rs48411062	snp	A/G	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77407830	GCTGTCTTTCAGAAT[A/G]ATTTTATATATGTGT	78514
rs48415231	snp	C/T			downstream-variant-500B	Arhgap10	Mm_Celera	8:77249930	TGGGCCATGCCTGGG[C/T]CTGGAGTTTGCACTT	78514
rs48415992	snp	C/T	0.142012	0.225474	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494243	CGTGTGTGAACACAC[C/T]ATTTCTATGACTAGA	78514
rs48416462	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77505774	TGCCGTAGTACTCCA[C/T]ACACAATGTCTCACA	78514
rs48426394	snp	C/T	0.408163	0.193609	intron-variant	Arhgap10	Mm_Celera	8:77481854	TGCAAACTAGTTGGA[C/T]GCTCTGAGCAAGTCA	78514
rs48436605	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77458347	CATCTCCTCGTTCTC[A/G]GGATCCATAATTTAG	78514
rs48440805	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77287683	CGTGGTGGTGCACAC[C/T]TTTAATCCCAGCACT	78514
rs48452736	snp	C/T	0.277778	0.248452	intron-variant	Arhgap10	Mm_Celera	8:77507547	GGCAGTCTGGCACCG[C/T]ATTCTTAAGAGATTT	78514
rs48456988	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77485100	TTCTACCAGTCACTC[A/G]CTTCTGTAAGGAACT	78514
rs48477104	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77419803	AAGGCCAGGATAGCG[A/G]GTTGTTACACAACAA	78514
rs48482626	snp	A/C/G	0.260355	0.249785	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485443	CTCCAGGGCTCACCT[A/C/G]CTCAGTCCCCAGAGC	78514
rs48484767	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77313663	TCTAATGGAGAAAAG[A/T]TGACCAGCCATGTGA	78514
rs48487187	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77457137	AGTTTGGAGCTGAAA[C/T]GAAAGGATGGACCAT	78514
rs48487616	snp	C/T	0.408163	0.193609	intron-variant	Arhgap10	GRCm38.p3	8:77457891	AGCGCACATGCATGA[C/T]ACACACAAAGATAAA	78514
rs48489964	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77469818	CTTGGGTTCAGGCTA[C/T]CGAAGTTGAATATGA	78514
rs48496433	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77405735	AATCCAAAAATAACA[A/G]TTGGATTCATTCTGA	78514
rs48496630	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77441964	TAAGAGAGATTGACC[A/T]CTCCCTCTGTAACCA	78514
rs48502801	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77446464	TGCGCTGGCCTTGCA[A/C]CCTTTATTAATTCCA	78514
rs48506728	snp	C/T	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77501389	CCATGACACGAGAAA[C/T]AGCATCGGGTAAGAC	78514
rs48516781	snp	C/T	0.18	0.24	intron-variant	Arhgap10	Mm_Celera	8:77473129	GTGGGACAACTAGGT[C/T]TGTTATACCAACAGT	78514
rs48520121	snp	G/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77403841	CCGTTCCGTCTCCAG[G/T]CTGGGTGGACGCCCA	78514
rs48522654	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77414184	CTAAAGCAGCTCGTG[A/G]CATTTTGGAAACTCA	78514
rs48523721	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77404362	AAGGATCCTGAGCCC[A/G]AGGAACCTGAGAAAG	78514
rs48529064	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77256051	AAAATTTACCAAACA[C/T]GGTAACACTTTGGTC	78514
rs48530124	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77410058	TTCATTTGGTCATCT[A/G]GAGCCGAAAATGGAA	78514
rs48540120	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77427091	AGCCCAGTTTGACTA[C/T]GTAATGCTCCACCCA	78514
rs48540848	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77352761	AACAAACCAAACCCA[A/G]TGCTCACTCAGAACA	78514
rs48542215	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77254157	TGGGATTCCTAAGCC[A/T]CAGAGAAAGGGGGCA	78514
rs48542753	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77314437	GGCTTCATTAACTTG[C/T]CTCCACTATTTTCTA	78514
rs48556569	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77415713	TCAGTTCTAATCTCG[A/G]GGGACCCTGGAAGAT	78514
rs48557633	snp	A/C/T	0.142012	0.225474	intron-variant	Arhgap10	GRCm38.p3	8:77388107	GGACCGAGTGCCAAC[A/C/T]GTCAGAATCCAGGTG	78514
rs48559895	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77455786	CATGGTAAGCAAGCC[A/G]GTAAGCAGTACCCCT	78514
rs48560671	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77254762	AAGCTATTGCATGAG[A/C]GCAAGAAAACAGCCT	78514
rs48563041	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77374239	TAACAGCCATTCTGC[C/T]CACCATCGTTTATTA	78514
rs48568278	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77251867	AGAAATACATACACC[C/T]CTGGTGAATCAGTGT	78514
rs48585249	snp	C/T	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77398517	GTCTGAATAAACTGG[C/T]ATAGTAGTCGGTGTG	78514
rs48589310	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77457159	ATGGACCATCTAGAG[A/G]CTGCCATACCCAGAG	78514
rs48607925	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77275468	GTTCTGGGGACTGAA[C/T]TCAGGTCCTCACGCT	78514
rs48608811	snp	C/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77409354	ACAGGTTAGAATGAT[C/T]CCAGTCTTCAGCCAG	78514
rs48618728	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77252175	TCACACTGCGGTTAT[C/T]GGCTTTGCCCCCATA	78514
rs48618992	snp	A/C	0.35503	0.226867	intron-variant	Arhgap10	Mm_Celera	8:77409849	ATACTGCTGGGATCA[A/C]AACACAGAACCACTG	78514
rs48624956	snp	A/G	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77495872	CCGCACAGCTGCTCT[A/G]ACAAAGTGACTTCTA	78514
rs48638475	snp	C/T	0.473373	0.11227	intron-variant	Arhgap10	GRCm38.p3	8:77488498	CACCACAAGGCCTCT[C/T]GCTGGAACAGAAAAT	78514
rs48641897	snp	A/C	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77400151	CAAGCATTCTCACAC[A/C]GTTAACAGGTTAGTG	78514
rs48649951	snp	A/G	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77460197	CAGGTGGGCATGGCC[A/G]GGAGCATTATGGGAA	78514
rs48652879	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77252251	CCTAAGAGGCCAGGG[G/T]GAGACTACAACTCAA	78514
rs48654710	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77427335	ATGACAGAGAAGCCG[A/C]TGCTCAGCTAGGTAA	78514
rs48693464	snp	C/T	0.142012	0.225474	intron-variant	Arhgap10	Mm_Celera	8:77456441	ACGAGCCCCAGCGCA[C/T]TCCTAAGCTGCTCTA	78514
rs48694171	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77457011	TACCCAAGATATAAG[A/G]TACAATTTGCGAAAC	78514
rs48701985	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77255332	GACAGCTGGCCACCC[A/G]CACTACAGTGCATCA	78514
rs48714407	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77251804	ACAACCCAGAACCAG[C/T]TGTGAAATGCAGCTT	78514
rs48719695	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77451280	GACTTTGAACTGATC[A/G]CCACCACCACCATCA	78514
rs48731065	snp	A/G	0.297521	0.245442	intron-variant	Arhgap10	Mm_Celera	8:77514339	TTTCCAATCTGACAA[A/G]GCTCTCTTCCTTATT	78514
rs48734356	snp	C/G/T	0.231111	0.249285	intron-variant	Arhgap10	GRCm38.p3	8:77404524	CAAAAGCAAATAAAT[C/G/T]TAACCAAGCCTCATC	78514
rs48753207	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77275691	CGCCCCCATCCAGCT[A/C]GAAAGTCAGAGTACT	78514
rs48764370	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77387817	CGTGTTACACGCTCT[A/G]AGACAGCTCCATTCT	78514
rs48767390	snp	A/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77388293	TGCACTTATTGACCC[A/T]TCTCCACAATCTAAA	78514
rs48774787	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77256647	TTTCCCTGCTTCCTA[A/G]GAACTCTTTTGGGGA	78514
rs48784556	snp	C/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77463608	TAAAAAGAAAACTTA[C/T]AGAGTAGAAAATATT	78514
rs48790376	snp	C/T	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77419034	TCACAAGTTGTTTTA[C/T]AGCCTACAAGTTACT	78514
rs48812607	snp	A/C	0.391111	0.206368	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484175	AGGACTTGGAGCCAC[A/C]GGGAAGACCAAACTA	78514
rs48828372	snp	C/G	0.165289	0.235211	intron-variant	Arhgap10	Mm_Celera	8:77396770	ACACTATACCAAGCT[C/G]CAATCATGCATCACA	78514
rs48849680	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77378384	TATTGGAGGACTGGC[A/G]TCTAGGAAGCAAGGC	78514
rs48872913	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77400852	TCCTTTCTGTGTCAA[A/G]GCCGTGACTCCTGGC	78514
rs48876212	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77511935	TAAGCGCACTGCACC[A/G]CCACACCTGGCTCGT	78514
rs48881037	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77497425	TCCGGCCAGAATTTA[C/T]ACCAATATTTACCCA	78514
rs48881545	snp	C/T	0.35503	0.226867	intron-variant	Arhgap10	Mm_Celera	8:77505761	CCTCACTAGTAACTG[C/T]CGTAGTACTCCACAC	78514
rs48882592	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77374800	CAGATGGACAGTTGT[C/T]CCTACTGCAACTGAG	78514
rs48889054	snp	A/G	0.35503	0.226867	intron-variant	Arhgap10	GRCm38.p3	8:77488831	CTAAGTAAGATGGGT[A/G]GCAGAGCAGTGGTAT	78514
rs48889535	snp	A/G	0.132653	0.220748	intron-variant	Arhgap10	Mm_Celera	8:77412178	CGGAGGCTGAACCAC[A/G]ATCCTAACTCTACCA	78514
rs48889756	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77328348	ATGTGTTCATGGCAG[C/T]CATTTCTTCTGTAAC	78514
rs48891584	snp	G/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77461263	CATAATGGCACGGTG[G/T]ACAGCAATTCTGCAA	78514
rs48898270	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77406537	AAAGCACAAGATGGA[C/T]CCCTGAAGCACCACA	78514
rs48899919	snp	A/G	0.486111	0.0821678	intron-variant	Arhgap10	GRCm38.p3	8:77459009	TGCGTGGGCCAATTC[A/G]TTCCCTCCTCCTCTT	78514
rs48915751	snp	C/T	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77498687	TGCAGAGCAACCAGG[C/T]AGGGTTTTCCTATTG	78514
rs48915952	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77401008	AGCTAAATCCGACTC[A/G]AGTCTCCGCCAATGT	78514
rs48917205	snp	A/G	0.42	0.183303	intron-variant	Arhgap10	GRCm38.p3	8:77459058	CAAAGATGGCTGACA[A/G]GCCGCAAGCATTTAT	78514
rs48923693	snp	A/G	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77468697	ATGAGTAAGTTGAGA[A/G]TCTGCCCAGCTGAGC	78514
rs48927466	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77456615	TCTTATTCCCAGAAT[A/G]AGCAGTATCTGAAGT	78514
rs48934763	snp	A/G	0.497041	0.0383476	intron-variant, utr-variant-5-prime	Arhgap10	GRCm38.p3	8:77492643	GCATTTAGTAACCCC[A/G]CTCAGCTGCAGAGAG	78514
rs48935376	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77288071	GAGGACTGACAGAGG[A/G]CAAAAGACACATAAA	78514
rs48935977	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	GRCm38.p3	8:77418234	AGCATCTCATGCCTC[A/G]CTCGACATGGCTCAG	78514
rs48936548	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77328673	TGGCTGGTTGGTTTC[A/C]ATTATACTAACACCA	78514
rs48938824	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77498463	ATCAAGAACTCATAT[A/G]CAGAAACGAGATCAC	78514
rs48946622	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77417640	TATCTGCCCTTATTT[A/T]AAAAAAATTAAAAAC	78514
rs48949774	snp	A/G	0.32	0.24	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484071	CTAGGAAGGTCATGC[A/G]GTCACAACCTGGTTA	78514
rs48950943	snp	A/G	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77501139	ACAACTGTTAGGCAT[A/G]TATCTGTCAAGTGCC	78514
rs48957627	snp	A/G	0.142012	0.225474	intron-variant	Arhgap10	Mm_Celera	8:77418053	GAATACATATCTCTG[A/G]ATTCCAAAATATATA	78514
rs48959817	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77474906	CAGAGGCTGGAGATA[C/T]CCCCAACAAAAGCAT	78514
rs48966498	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77369239	GGATTAAAGGTGTGC[A/G]CCACCACACCCGGTC	78514
rs48966797	snp	C/T	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77500864	CATTCATACCAATCC[C/T]GCAAGGCTGGCATTC	78514
rs48974724	snp	A/G	0.42	0.183303	intron-variant	Arhgap10	Mm_Celera	8:77474225	TGGGTGGTCTGCTCC[A/G]TACGAAGTCAGATTA	78514
rs48990216	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77252012	ACCATTTGTTTTCCC[C/T]GTTGCGAGAAGTTCT	78514
rs48990368	snp	A/G	0.142012	0.225474	intron-variant	Arhgap10	Mm_Celera	8:77398761	TTAATAGATGCAATA[A/G]ATGTCTGTTGTCTTA	78514
rs48994964	snp	G/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77403460	GTGGCATCAGCACGT[G/T]TCAGCCCGTGGTGTT	78514
rs49001759	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77372862	ATCAATCGCATCCGC[C/G]CTTCCACCCGAGTCC	78514
rs49002899	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77448227	TAAACCAAGATGCTT[C/T]ATTACCAGCCCACAC	78514
rs49012186	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77507107	TGAGAAGCTGAGTTT[A/G]GATCCCACAGCACGC	78514
rs49021086	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	GRCm38.p3	8:77468302	GCCTCTAAACTCACT[A/G]GCTTGGCAAGCTGGA	78514
rs49025658	snp	A/C	0.391111	0.206368	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484140	TGAAGAATCCTAAAT[A/C]GAATCCACTGCGCTC	78514
rs49027180	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77516217	CTCTGTTTCCCACCT[A/G]GAACAGAAAACCTCA	78514
rs49029241	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77456126	AAATCTGCCAACAAG[A/G]GAAGTACACATTCAA	78514
rs49032352	snp	A/G	0.35503	0.226867	intron-variant	Arhgap10	Mm_Celera	8:77461321	AGGGTTTAGCTGTCA[A/G]CTACCTGCAGAAAGG	78514
rs49036327	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77511699	GCAGAGGCAGAGGCA[A/G]GCGGATTTCTGAGTT	78514
rs49044665	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77506442	ATGCATTGAATTCAG[A/T]TGTCCCCACTCAAAA	78514
rs49049040	snp	A/G	0.142012	0.225474	intron-variant	Arhgap10	Mm_Celera	8:77461421	ACAGAGAGAATCAGA[A/G]GTGGCCGATGGAAGC	78514
rs49056421	snp	A/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77470607	AGTGCTGATGAGGTA[A/T]ACTGTCTCTATGAGC	78514
rs49059191	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77459349	AACATAATTTAATCA[A/G]CTACTTTATCACAGG	78514
rs49072740	snp	A/C	0.124444	0.216185	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77502745	TGCTGAAGAACTGCT[A/C]GATCAACAGGTGGGA	78514
rs49074146	snp	C/T	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77489118	GTCTCAGTGAGAGAG[C/T]CTGTCTCAATCTATC	78514
rs49074361	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77422676	ACGTGGGTGGTGGGT[A/G]GAGGTGAAGGTCCTT	78514
rs49082459	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77398849	TCAAGTGCCTTTTAG[A/G]GAAAGGACAATAAAA	78514
rs49082682	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77457046	GAAGCTCGGAAGAAC[A/G]AAGATCAAGGTATGG	78514
rs49093720	snp	G/T	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77487075	AGGCTAGACTCTTGA[G/T]CAACTAGTCACACTG	78514
rs49096748	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77353168	AAAGTGTTTGGGACG[C/T]GAACAGCCATATCCA	78514
rs49113584	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77275755	AGCTGGGGAATTCAC[C/T]CTTCCTTTGATTTAT	78514
rs49122521	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77417139	TCCTGATAATCCCGA[C/G]ACCCCTCCTGCTTTC	78514
rs49126340	snp	C/T	0.32	0.24	intron-variant, utr-variant-5-prime	Arhgap10	GRCm38.p3	8:77492396	ACATTTGCCCAGATC[C/T]TGCACATGATAGGTT	78514
rs49131422	snp	C/T	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77416088	AAGATGGGAGTCAGA[C/T]GCCTTTAATCAGAAT	78514
rs49146955	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77374773	GTCCCTACTGCAACT[A/G]AGGCTCACATGCAGA	78514
rs49149961	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77417195	CACAAAAGTGCAAAG[C/T]GAGCTTTCTAAAATA	78514
rs49164135	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77274548	TTTGGTGATAGCACA[A/G]TTGGGATTTAAGAAA	78514
rs49168128	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77418366	AGCCTGGGCTAAATC[A/G]AGATGGCTTCCCTGG	78514
rs49169254	snp	A/G	0.46281	0.131194	intron-variant	Arhgap10	GRCm38.p3	8:77459459	CCTCAGACTGACTCA[A/G]GAGGTCAGGGATCTG	78514
rs49174272	snp	G/T	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77406871	AGGAATGATGGCATC[G/T]GCAACTGTACGCAGT	78514
rs49184358	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77416558	AAGAAGGCAGAGGAG[A/C]CAGCATGAGAGGATT	78514
rs49192831	snp	C/T	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77514371	TAAGACATCGCTGAG[C/T]TCTGAAACGCCAGGG	78514
rs49206174	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77401655	GAAACTTAAATTTTT[A/G]TACGACTCACTATTC	78514
rs49210835	snp	C/T	0.142012	0.225474	intron-variant	Arhgap10	Mm_Celera	8:77400269	TTTATGCTACCAGAT[C/T]TTAATTCCATCCAAG	78514
rs49220109	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77457051	TCGGAAGAACAAAGA[C/T]CAAGGTATGGACACT	78514
rs49220609	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77319914	TCAAGAGGCTGAAAA[C/T]GTCCTACCTCAGGCT	78514
rs49221992	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77471955	GCAAGGACTGGTGAT[A/G]TAAACCAGATCACTT	78514
rs49223316	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77388475	AATAATGGCCCCAGT[A/G]TGCGTGTGCTGCAGC	78514
rs49224487	snp	A/T	0.46281	0.131194	intron-variant	Arhgap10	Mm_Celera	8:77407892	TTTTGCTATATATAT[A/T]AAAAAAAAGTAGAAT	78514
rs49229501	snp	C/T	0.297521	0.245442	intron-variant	Arhgap10	Mm_Celera	8:77412078	TTGAACGAGCTTTGG[C/T]TTCTTTAATTTCCCA	78514
rs49235895	snp	C/T	0.391111	0.206368	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484210	CCAATGCTCTAGCCG[C/T]AACTTACAGGGAGTT	78514
rs49236735	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77324014	CCTCCACCCCTTCCA[C/T]AGGAGCATGCTCTCC	78514
rs49240914	snp	A/G	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77500095	CTACAAACTTTGTAC[A/G]CTTACTTGGTCACTC	78514
rs49248917	snp	A/T	0.132653	0.220748	intron-variant	Arhgap10	Mm_Celera	8:77467634	GATTCACCTTCCAAA[A/T]GCTGCTTTTATCAAT	78514
rs49252829	snp	A/T	0.124444	0.216185	intron-variant	Arhgap10	GRCm38.p3	8:77486768	TCTTAGTTGGCTTTC[A/T]ACACTATCACAAAAT	78514
rs49254363	snp	G/T	0.197531	0.244432	intron-variant	Arhgap10	Mm_Celera	8:77445087	GGTCTGGAGTAGGCA[G/T]ATGAACATGCTGCTG	78514
rs49256586	snp	C/T	0.152778	0.230321	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485497	TCTGCCTTCAGAGCA[C/T]TCCTCTCCACTCCCG	78514
rs49258611	snp	A/G	0.42	0.183303	intron-variant	Arhgap10	Mm_Celera	8:77506567	TTAAAATCCTTTTTT[A/G]GATTTACAACAGTCA	78514
rs49262286	snp	A/C	0.48	0.0979796	intron-variant	Arhgap10	GRCm38.p3	8:77478073	CCAGATGTTTTAGAG[A/C]TATCTATAGCAAACA	78514
rs49265034	snp	A/C/T			intron-variant	Arhgap10	GRCm38.p3	8:77490330	CAGGCCCCTCTCCTC[A/C/T]TCACCCGGCAGGGGC	78514
rs49272281	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77372499	TGGTAGTCTATAAAT[A/G]TATCAACTCAACTCT	78514
rs49281291	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77287666	GCCATGCTCAAGCCG[G/T]GCGTGGTGGTGCACA	78514
rs49282577	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77318173	GGGTATTTTAGTACA[A/C]CAATAAGAAAAGCAA	78514
rs49293315	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77372124	AGCTCTCTCTTTCAG[G/T]GTGGACAGCCCCAGG	78514
rs49303185	snp	C/G	0.277778	0.248452	intron-variant	Arhgap10	Mm_Celera	8:77460933	AAGACACTGGGACAG[C/G]CAGCATGCCTTTTAG	78514
rs49303468	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77372807	CCTAAGCCACTCACT[C/G]GAGTGTGAGGCCCTG	78514
rs49306154	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77371604	ATTTTTACACTCTCA[C/T]TTTTACAATGCACTT	78514
rs49312217	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77490577	CAGGGATCCGAGCTG[C/T]TTCCTAGAAGAGACT	78514
rs49312524	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77428970	TAGATTTTCTTTAAC[A/G]TGACTATCTTTGTAT	78514
rs49317722	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77512256	TCTGAATGAGCAACG[A/G]CCTGCTGCTCGGAGA	78514
rs49322161	snp	C/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77408686	TTTTCAAACAACGCA[C/T]TCTTTCTCCCGCGAT	78514
rs49322559	snp	A/T	0.132653	0.220748	intron-variant	Arhgap10	Mm_Celera	8:77404584	TCTTAACTGCTATTT[A/T]AGACCAAATGTTTGC	78514
rs49328035	snp	A/T	0.297521	0.245442	intron-variant	Arhgap10	Mm_Celera	8:77496028	GATAGTTGTTTGGTT[A/T]TTTTAAGAAGGAGCA	78514
rs49330749	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77367289	GCCACCTATAGGCGA[G/T]GGGGAAACATGCAGA	78514
rs49337490	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77254011	AAACCAACCAATACA[C/T]CGGACCACATGGGGA	78514
rs49337971	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77513483	CCAAATCGCGGTACA[A/G]TGTGTAAGGGCAACT	78514
rs49339320	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77255389	TATGCAACCATATCT[A/G]CAGCATACCGTGAGG	78514
rs49347373	snp	C/T	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77499998	GATAGGACCACAGAA[C/T]GCAGCTCTACGGTTG	78514
rs49350283	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77372725	GTCCACACCTTCTAA[C/T]GCGCTCTTCAAAGAT	78514
rs49361530	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77427657	TGCCTCCACCGCAGC[A/G]CCCATTTAAAAGCGG	78514
rs49385097	snp	C/T	0.48	0.0979796	intron-variant	Arhgap10	Mm_Celera	8:77481802	AAACTACCAGGAAGT[C/T]TCTATGTGAATTTCC	78514
rs49385475	snp	A/G	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77417055	ACAGGGAAAGGAGTC[A/G]TTGTTATTCTTCTAT	78514
rs49386883	snp	A/C			downstream-variant-500B	Arhgap10	Mm_Celera	8:77250175	CCAGTTCCCATCCCA[A/C]GGTCTCTTGTGGGAA	78514
rs49396044	snp	C/G	0.336735	0.234472	intron-variant	Arhgap10	GRCm38.p3	8:77489557	AAAAAGGCATTATGC[C/G]AGTTTACCCACCCAA	78514
rs49400794	snp	A/G/T	0.142012	0.225474	intron-variant	Arhgap10	GRCm38.p3	8:77387791	GCTGAGCCACCAGCC[A/G/T]AAAGCAGCACCGTGT	78514
rs49402279	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77369350	TTAAACAAATGCAGA[C/T]CTATACTTTACCATG	78514
rs49404330	snp	A/C	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77413134	TCAACTCTGCTGAAT[A/C]ATCCCTCCAGCACCT	78514
rs49414896	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77498232	TCCTGGCAACACTTT[C/T]TGAGGATACAGTTGC	78514
rs49423594	snp	C/G	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77461592	GACACTGGCTCTGCT[C/G]TGGTACACACCAAAC	78514
rs49426059	snp	A/G	0.152778	0.230321	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485522	CTCCCGTCCTTCAAA[A/G]CCAGACCAGACTTTG	78514
rs49427622	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77424820	CTAGGCTAAAGAGGT[A/G]GCTGAGTGTTTAAGG	78514
rs49428257	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77402789	TCCGACCTGAGATGT[A/G]CACTTCGACCTGAGA	78514
rs49430847	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77507345	CATACCTACAGTCAC[A/G]AAACTCCCCATCTTA	78514
rs49446899	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77467825	CCGCATCAGAGCTGA[A/G]AACTTTCTCACAGCA	78514
rs49448096	snp	C/T	0.18	0.24	intron-variant	Arhgap10	Mm_Celera	8:77451175	CTCTCCTCAATCAGG[C/T]CAGAATGTATTCCAA	78514
rs49451951	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77504471	TCCTTCTTTTGTGAT[A/G]GACATAACGGTGTAG	78514
rs49454086	snp	A/G	0.5	0	intron-variant	Arhgap10	GRCm38.p3	8:77460413	ATATTAGCAAGAAAG[A/G]AACATTTTCCAAGAG	78514
rs49467185	snp	A/G			downstream-variant-500B	Arhgap10	Mm_Celera	8:77250006	GCTGTCAGCCTACCC[A/G]TCCCAAAGCCCAGCT	78514
rs49475579	snp	C/T	0.42	0.183303	intron-variant	Arhgap10	Mm_Celera	8:77513581	CTAACTGAAATAAAG[C/T]ACAGGCCACTAAGTC	78514
rs49484437	snp	A/T	0.260355	0.249785	intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77492732	ATTTTCTCCTAGAAG[A/T]CAACAAATTAAATAG	78514
rs49488189	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77484030	TCACTCCTCCCTTCC[C/T]CTTGCTTCTGACAGG	78514
rs49490412	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77407135	ACATGTATACGATGC[A/G]CAGACATCTATCCAA	78514
rs49492576	snp	C/T	0.18	0.24	intron-variant	Arhgap10	Mm_Celera	8:77446315	CTCCAACGACACGAT[C/T]GTATCTTCATAAGCT	78514
rs49492694	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77475158	AGAGAGGAAGGGGGG[A/C]TTCAGTAGCCCAGCT	78514
rs49498934	snp	A/G	0.35503	0.226867	intron-variant	Arhgap10	Mm_Celera	8:77469567	GACGGGAGAGTATGT[A/G]CTGGGCTGGAAGGGT	78514
rs49507297	snp	C/T	0.132653	0.220748	intron-variant	Arhgap10	Mm_Celera	8:77458462	AGGTGCTCCACTGTG[C/T]GTTATCAGTTCAGTT	78514
rs49520453	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77450615	TGCATCAAAACTTCT[A/G]TCAGGCTCAGCTCCA	78514
rs49522538	snp	A/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77486209	CTTCGACAAGGAAGC[A/T]TTACATTGTCACATA	78514
rs49527526	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77338569	TTGCCTAACTCCTAG[A/C]ATCCTTCCCATTGGC	78514
rs49536553	snp	C/T	0.495868	0.0452663	intron-variant	Arhgap10	Mm_Celera	8:77511088	GAAAAGCTAGAGGAC[C/T]GGTCTGTAAGCCACA	78514
rs49544761	snp	C/T	0.152778	0.230321	intron-variant	Arhgap10	Mm_Celera	8:77461614	ACACCAAACCACTGT[C/T]CCCTGCCTGACAAGG	78514
rs49551750	snp	A/G	0.408163	0.193609	intron-variant	Arhgap10	Mm_Celera	8:77473535	ACAAGGCAGTGTGGC[A/G]CTCAGCCAGCGAGGT	78514
rs49557983	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77504216	ACCACCACCATTGTG[C/T]GGTGCTTCCCACAGC	78514
rs49567059	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77476906	AAGTGACGTGGGTAC[A/C]AGCCTATGAGACCAC	78514
rs49574666	snp	A/G	0.32	0.24	intron-variant	Arhgap10	GRCm38.p3	8:77488510	TCTTGCTGGAACAGA[A/G]AATCTATAAACATTC	78514
rs49579226	snp	C/T	0.497778	0.0332592	intron-variant	Arhgap10	Mm_Celera	8:77407525	GACCCCTGACTAATG[C/T]CGGTAAGGACCACAG	78514
rs49585372	snp	C/G	0.277778	0.248452	intron-variant	Arhgap10	Mm_Celera	8:77487756	AGAGAAACAGGCTGT[C/G]GGTGTGTGAAGAAAG	78514
rs49596638	snp	A/C	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77454961	ATAGCAGAGCCATCT[A/C]GTTAAAGCCATGGAA	78514
rs49600675	snp	A/G	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77414440	ACAATGAAAGGGGCC[A/G]CCATGGCTCCTGAGG	78514
rs49611295	snp	A/T	0.18	0.24	intron-variant	Arhgap10	Mm_Celera	8:77505809	CCACAAACCTAAGAC[A/T]ACCAAATGAACTGCA	78514
rs49616394	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77271752	GATTACTTGTCAAGG[A/T]CCCAGCTCCATCAAT	78514
rs49625570	snp	A/G	0.46281	0.131194	intron-variant	Arhgap10	GRCm38.p3	8:77461057	CCACCATATACCTCT[A/G]CATACATGATGTCGT	78514
rs49628506	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77353098	TTCAAGTCAAAGGCA[A/G]TACATTCTTTGATTT	78514
rs49632260	snp	C/G	0.35503	0.226867	intron-variant	Arhgap10	Mm_Celera	8:77413741	CTCAAAAAAATGTTT[C/G]TTCTTTCCAGTGTGT	78514
rs49658777	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77472820	CCCAGTTCCTATGGT[A/G]AGACAGGAGACGGAG	78514
rs49679007	snp	A/T	0.165289	0.235211	intron-variant	Arhgap10	Mm_Celera	8:77418645	TTCTGTTCTCATTTT[A/T]CACGAGTCCCATAAT	78514
rs49679312	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77483787	CTCAAGCCTCTCCCT[A/G]CTGCCTTTTCTGTGG	78514
rs49679843	snp	A/C	0.408163	0.193609	intron-variant	Arhgap10	Mm_Celera	8:77513453	TTACAGAGAACTGAA[A/C]TTCTTCTCGTTCTTC	78514
rs49685386	snp	C/T	0.277778	0.248452	intron-variant	Arhgap10	GRCm38.p3	8:77460402	ACAAAGTAGCAATAT[C/T]AGCAAGAAAGAAACA	78514
rs49689499	snp	C/T	0.132653	0.220748	intron-variant	Arhgap10	Mm_Celera	8:77387770	GCTTTCGACAATGCC[C/T]CTGCGGCTGAGCCAC	78514
rs49694336	snp	C/T	0.260355	0.249785	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493786	CATACTGCCAACACT[C/T]GACCACAGATTCCTG	78514
rs49698371	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77278823	ACTGACTCCTGACCC[A/G]ACTCAGAGCTAAGGC	78514
rs49709214	snp	C/T	0.165289	0.235211	intron-variant	Arhgap10	Mm_Celera	8:77451644	TGACTAGGGTAAAAA[C/T]GCTAAAGACGGCTGA	78514
rs49727654	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77372207	AGCAAAGCTTCAGGA[A/G]AACACAGAAGAACTC	78514
rs49729527	snp	C/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77410091	TATCGCTAAGGAGAA[C/G/T]TGCCCTAAAACCCCA	78514
rs49732095	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77404760	AGGAACCATGCAGAA[A/G]CCTTTTTTTTTTTTT	78514
rs49740693	snp	C/T	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77406571	GACAGCAGGCCTGCC[C/T]GCAGAGAATACTGCA	78514
rs49766425	snp	G/T	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77456532	CAGTATCTGGTGACA[G/T]CGAGCGGAAAGTGTT	78514
rs49769476	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77507285	GTGATAATCAGGATA[A/G]CCGGATGGTCTCCTC	78514
rs49781032	snp	A/G	0.497778	0.0332592	intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77484150	TAAATCGAATCCACT[A/G]CGCTCCTCAAGGACT	78514
rs49790308	snp	C/T	0.132653	0.220748	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494148	AAGTTGTAAGTAAGC[C/T]CAAAGCAAGGGAGAG	78514
rs49804480	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77457171	GAGGCTGCCATACCC[A/G]GAGATCCATCCCATA	78514
rs49807009	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77397532	GTGGCTATCTGTAGA[A/G]CGCACAGTTGGAATT	78514
rs49816972	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77408417	CAGTAGTTTTAAAAG[A/G]CTTGTCCTTCCGGGC	78514
rs49840049	snp	C/T	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77396569	GAAAACACATGAACA[C/T]ACGAATTGAACAAGG	78514
rs49851714	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77374387	GTCCTGGCCCATTCA[A/G]CTGCTCACAAAGCAC	78514
rs49867767	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77449739	AGTGGAGAAGCTCAG[A/G]GCTCCATCCCCCTAC	78514
rs49888818	snp	A/G	0.46875	0.121031	intron-variant	Arhgap10	Mm_Celera	8:77512920	GAGATTGGAATCTTC[A/G]TTCTTTTCGTTTATC	78514
rs49889553	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77319660	CTTCAAACAGAAGTG[C/T]ATGCTAGAATGGGCT	78514
rs49890261	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77444059	AAGGTGCCTCTGGGC[G/T]CCCCTGGAAAGCTCC	78514
rs49902669	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77352798	AGAGCCTGAAATACA[C/T]GAGTAGAATCTAACA	78514
rs49909267	snp	A/C	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77398442	CCTTGACATGGGAAA[A/C]CGGTTCCTTTTCAGT	78514
rs49911066	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77281899	GGATTTGGCTAGAGT[A/G]TGGGGGCCAGGCAGA	78514
rs49917426	snp	A/C	0.444444	0.157135	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503791	TACCCATTACTCCAT[A/C]GCCCACGGCGACAAT	78514
rs49918791	snp	A/G	0.152778	0.230321	intron-variant	Arhgap10	Mm_Celera	8:77471585	CCATCTCTCCAGCCC[A/G]CAGCAGCCAGTGCTC	78514
rs49930785	snp	A/G			downstream-variant-500B	Arhgap10	Mm_Celera	8:77250162	TCACTACCACAGACC[A/G]GTTCCCATCCCAAGG	78514
rs49932032	snp	A/C	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77467813	TGCGATTTTAATCCG[A/C]ATCAGAGCTGAGAAC	78514
rs49934636	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77457233	CACTAGCAAGATTTT[A/G]CTGAAAGGACCCTGA	78514
rs49945796	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77405163	AGACAGCCCCAGCTC[A/G]TGGGATTCATAATCT	78514
rs49948614	snp	C/T	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77388775	GTCACCTAGTGACAA[C/T]GCAAACCCTCTCCTC	78514
rs49950379	snp	A/C	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77388534	TACAGTTCCAAGATG[A/C]GTTCAAACACCAGCT	78514
rs49959543	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77287160	TTATTCATATACAAA[G/T]CTTGATGAGAAAAAC	78514
rs49961127	snp	A/C	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77499972	AACTGATGGGCAAAC[A/C]CAGTCTAAAGGATAG	78514
rs49978902	snp	C/G	0.244898	0.249948	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493966	AGGCCAAAATATAAA[C/G]GACTGTGTCTAATCT	78514
rs49994051	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77253956	TAATCTGGTCCATAG[A/C]TGTTGCAACAAACAG	78514
rs49994390	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77443710	TTATAGCCGGGCGTT[A/G]GTGGCGCACGCCTTT	78514
rs49998858	snp	A/G	0.165289	0.235211	intron-variant	Arhgap10	Mm_Celera	8:77510989	CATCGTCAGAATGTG[A/G]CTCTTTCCAGAGTCT	78514
rs49998985	snp	A/C	0.391111	0.206368	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77502558	TCTTCACCATTCAAA[A/C]AAGCCAGGTGTGACG	78514
rs50020320	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77476828	CTGTTATTGTTGAGA[C/T]AGGCTCCTTGACATG	78514
rs50034625	snp	A/G	0.426035	0.177515	intron-variant	Arhgap10	GRCm38.p3	8:77458932	TTCAAGTATTTGCAC[A/G]TCTGCCTGAAGAATC	78514
rs50034691	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77352946	TCCCCACCTCCCTCA[C/T]CCAAGTACATGTCCT	78514
rs50042115	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77410046	ACTCTACACTGCTTC[A/G]TTTGGTCATCTGGAG	78514
rs50046699	snp	C/G			downstream-variant-500B	Arhgap10	Mm_Celera	8:77249987	AGAATCTCATGTTGG[C/G]ATGGCTGTCAGCCTA	78514
rs50048772	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77369394	CAGTATATAGCTCAC[C/T]AAGAAAAATACTCAT	78514
rs50056497	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77353113	GTACATTCTTTGATT[A/T]CAATAAGAGTGGAGA	78514
rs50058686	snp	A/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77498545	CTCTGAGATACAAGG[A/T]CATGGACAGGGACTT	78514
rs50080118	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77374629	cctgaggggcagtta[C/T]atgttactcttggtg	78514
rs50103288	snp	A/T	0.336735	0.234472	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484348	AATAATTGTGAATGA[A/T]CAGGGAAGAGACTAA	78514
rs50106914	snp	C/T	0.132653	0.220748	intron-variant	Arhgap10	Mm_Celera	8:77407927	TTCTTGTAAGTTCTG[C/T]TTTAGTTCTTCGTCT	78514
rs50111458	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77457717	TCCCACTAGAAAGTC[C/T]ACACTCAATAGCACC	78514
rs50118829	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77480153	CCTTAGGGCCAGGCC[A/G]CTGGGGATGCAACTT	78514
rs50124804	snp	A/G	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77487506	ACCTGACATGCCTGA[A/G]GAACCAACCAGAAGA	78514
rs50136747	snp	A/C/T	0.5	0	intron-variant	Arhgap10	GRCm38.p3	8:77478779	AGTGGTCACTGGTCG[A/C/T]GAGCCTAGGAGGCCC	78514
rs50147040	snp	C/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77402620	AAAAGGTCTGGAGAC[C/T]GTCGGCTGGTAGCTC	78514
rs50152954	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77410602	ACCTTATGAAAACTC[C/T]GCGTGCCTAACTGAG	78514
rs50153168	snp	C/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77498337	GGGAGGAACCACAGA[C/G]TGGAACCAAGTGAGG	78514
rs50165744	snp	A/G/T	0.244898	0.249948	intron-variant	Arhgap10	GRCm38.p3	8:77418127	CACAATAAAGGACGG[A/G/T]TGTTGCTGTCAGCCG	78514
rs50173693	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77252234	TCCACATTCCATGAG[C/T]ACCTAAGAGGCCAGG	78514
rs50177385	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77504490	ATAACGGTGTAGACA[C/G]TAATTCAGATCATCT	78514
rs50178065	snp	C/T	0.132653	0.220748	intron-variant	Arhgap10	Mm_Celera	8:77473011	CTATCCCTTACACAG[C/T]CCTAGTGTCCACACT	78514
rs50196324	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77457787	ATACCCACTGCTCAG[A/G]GGTAAGGATCGACTG	78514
rs50198316	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77409348	GACAGCACAGGTTAG[A/G]ATGATTCCAGTCTTC	78514
rs50200992	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77288276	CAGGTCCTGAAAGCA[C/G]GCCAACATATTGGCT	78514
rs50205607	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77443492	GACAAGCCTAAAGTC[C/G]GGTCTCCTGTGCAAT	78514
rs50211721	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77450928	AGCTGACAGACCTAA[A/G]AAGAAAGGCACACTG	78514
rs50219983	snp	A/G	0.396694	0.202437	intron-variant	Arhgap10	Mm_Celera	8:77505954	CAGTTTGTGTTCACC[A/G]AGCTGAATATCAACA	78514
rs50241048	snp	C/G	0.32	0.24	intron-variant	Arhgap10	GRCm38.p3	8:77488899	AAGCATTCTATTAGG[C/G]TCAACAATGCCACCA	78514
rs50244407	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77504555	TGTCTTAGTCACCAG[A/G]AGCAGGACAACACTG	78514
rs50270974	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77255036	AGATAAAAGTGTGTA[C/G]AGTAAGGAAAGAATG	78514
rs50301247	snp	A/C/G	0.495868	0.0452663	intron-variant	Arhgap10	GRCm38.p3	8:77461071	TACATACATGATGTC[A/C/G]TGGGCAATCTTCATT	78514
rs50303533	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77448769	CCTGTGCACACTGCC[A/G]CATCCCTGGCCCTGT	78514
rs50304788	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77459062	GATGGCTGACAGGCC[A/G]CAAGCATTTATTATG	78514
rs50304954	snp	A/G	0.375	0.216506	intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77493791	TGCCAACACTTGACC[A/G]CAGATTCCTGTAGCC	78514
rs50307380	snp	A/C	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77497836	TTCATTTGGATTATG[A/C]AAATTTTGTTCAAAA	78514
rs50313510	snp	A/G	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77490138	CAGTGGGGTTCTCAG[A/G]CCCACACTCCCAGGT	78514
rs50313629	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77314820	ATCACTCGTGCCAGA[C/G]GTGAAGGACTGTCTG	78514
rs50320458	snp	C/T	0.277778	0.248452	intron-variant	Arhgap10	Mm_Celera	8:77506526	TTACAAATTCACCTC[C/T]GTTTTTCTAGACACA	78514
rs50322703	snp	C/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77400825	TCTGCCTCATGTTGA[C/T]GGTCCCGAGATTCCT	78514
rs50350412	snp	A/C	0.132653	0.220748	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484259	GACTGAACACGGGGC[A/C]TCACACACGCTAAAT	78514
rs50356911	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77255426	TCTCTCAAGTGGCAA[C/T]AGTAATCAAAGCTCA	78514
rs50359482	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77253624	ACAGGCCCCATGCAA[A/G]ATGTGTCTTGAGGAT	78514
rs50359929	snp	A/C	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77397589	TGGAAGCAGTACCTG[A/C]ACTTCAGAAGCACCT	78514
rs50368160	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77489499	GCAAGCCTGAGGAGA[A/G]CACACACACACACAA	78514
rs50372923	snp	A/C	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77513579	GCCTAACTGAAATAA[A/C]GTACAGGCCACTAAG	78514
rs50383053	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77448691	CCTGTGCACACTGCC[A/G]CATCCCTAGCCCTGT	78514
rs50394409	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77457368	AGGAAGTACCCAGGG[A/G]GCTGGGGGGGATCTG	78514
rs50399637	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77455857	TTGAGTTCCTGTCCT[A/G]ACTTCCTCTGCTGGT	78514
rs50400039	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77256822	CATAGCTCCTAAATG[C/T]CTGTGTATGAATATT	78514
rs50410176	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77471848	AATAGACTGAAGAGC[A/G]GAGGGCTTTATAGAC	78514
rs50415431	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77255164	TGAGAGACTTGGGGA[A/G]GCACCTGTAAGACGC	78514
rs50419861	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77403870	CACTGCTCACTACGA[A/G]AATACACCACTCCTG	78514
rs50427858	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77483759	TGGCACCACTCTGGG[C/G]TATCTGCTGTGCCTC	78514
rs50438126	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77320189	GATGGATCTCTGTGA[A/G]GGCCAGTTTGGTCTA	78514
rs50454638	snp	C/T	0.152778	0.230321	intron-variant	Arhgap10	Mm_Celera	8:77395698	AGTCAGAACACGCAT[C/T]ACCAATCTTCCTTCT	78514
rs50460118	snp	C/G	0.32	0.24	intron-variant	Arhgap10	GRCm38.p3	8:77488806	CACTTTTCTGTACAT[C/G]GGTTCCCTACTAAGT	78514
rs50470961	snp	G/T	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77415373	CATCTCAGACTTCTG[G/T]GCAGGCAGACTTGGG	78514
rs50480332	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77408712	GCGATCTTGGCAAAC[A/G]CTCCCTGTCTACTTG	78514
rs50487101	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77252222	CCTCATGCTGCCTCC[A/G]CATTCCATGAGCACC	78514
rs50492052	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77449488	TTGTATGGCAGGCAC[A/G]TTACCAAATGAGACA	78514
rs50497679	snp	C/G	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77461165	AATCAAGAGTTACTA[C/G]AGTGTCCTGTCAGAA	78514
rs50504031	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77425080	TCCAGCTCCAGAGGA[C/T]TCACCACTCTTCTGG	78514
rs50510870	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77403208	AGGCAGCATCGCGGC[A/G]AAGAACCTGGATGTG	78514
rs50517736	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77409994	GTTAAAAATACTTTA[A/T]AAGATCCCAGATAAA	78514
rs50526939	snp	A/C	0.46281	0.131194	intron-variant	Arhgap10	GRCm38.p3	8:77460379	TATATGAAAACTAGA[A/C]AAGAGGTACAAAGTA	78514
rs50527987	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77417118	TTCATCTATCACCTG[G/T]AGGCTTCCTGATAAT	78514
rs50533728	snp	C/T	0.396694	0.202437	intron-variant	Arhgap10	Mm_Celera	8:77485994	ACAGTTATGAAGTAG[C/T]AATAAAAATAACTGT	78514
rs50552342	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77424409	ATCAGGTAGAGCCAC[A/G]CATGGCTTCCTACAG	78514
rs50553775	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77500899	GAAAACAGACGGTAA[C/T]GGACACAAAACTAAC	78514
rs50576699	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77372871	ATCCGCCCTTCCACC[C/T]GAGTCCTCCAGGGGG	78514
rs50580527	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77496316	AGTCACCTTGCCCTT[A/G]CAAAGTCACACCTGC	78514
rs50583844	snp	A/G	0.142012	0.225474	intron-variant	Arhgap10	Mm_Celera	8:77388975	ATGTAGCTCAAGCTG[A/G]TCTTGAATTCAATCT	78514
rs50599219	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77271553	CAGAAACCCCGACTT[C/T]GACAGAGAGGAACCA	78514
rs50600679	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77347149	TGCACTGGTTATCAG[A/T]ATGTGAAGCGGGACC	78514
rs50605467	snp	A/C	0.46875	0.121031	intron-variant	Arhgap10	Mm_Celera	8:77513615	AAGGCCTCAATCTAT[A/C]AAGACTTAGTCTGGG	78514
rs50617514	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77403043	TGAACAGGCTTTCCA[C/T]GCCACCTCATGCTTC	78514
rs50618199	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77319878	TATAGCAGCTTCCAG[A/G]TGGCTGCCCCCAACA	78514
rs50620535	snp	A/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77372749	CAAAGATGAGCCCAT[A/G/T]GAGCTTCCATCTCCT	78514
rs50621320	snp	A/C	0.152778	0.230321	intron-variant	Arhgap10	Mm_Celera	8:77460739	CACGTTCTTTGCAAA[A/C]CTTAGAAGACACCAA	78514
rs50637269	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77422598	CATTAAAAACCAAGA[A/G]GGATGTAATCTTCTC	78514
rs50644011	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77341408	ACGCAGAGGAACTTC[A/G]TCTCCTCCTCACTCC	78514
rs50644532	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77424722	TTAAGAACAAGCAAA[C/T]GGACAGAAAGCAGTT	78514
rs50654308	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77322379	GACTGCAGGGGAGCA[C/T]GGTCAGAAGAGAAAG	78514
rs50660192	snp	A/G	0.408163	0.193609	intron-variant	Arhgap10	Mm_Celera	8:77459906	TGACGTTCATTTTGC[A/G]TGCCCCCTGGGCCAC	78514
rs50665437	snp	C/T	0.48	0.0979796	intron-variant	Arhgap10	GRCm38.p3	8:77511648	TTTTTAGGACAGAGT[C/T]TCGGCCGGGCGTGGT	78514
rs50669159	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77422395	AACAATACAAAATGA[A/G]CTTGCACACACAGTA	78514
rs50671226	snp	C/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77497439	ATACCAATATTTACC[C/T]ATCATTGTCCTTTGA	78514
rs50675246	snp	C/T	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77501463	AAGCAGAAGTTATGC[C/T]TGGAAAGAAGCTACG	78514
rs50676956	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77457063	AGATCAAGGTATGGA[C/T]ACTTTGCCCCTTCTT	78514
rs50677297	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77319596	GATAATCTTCATTAA[C/T]AGGGGACATGAATGC	78514
rs50684126	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77489134	CTGTCTCAATCTATC[A/G]ATCAATCAATCAATC	78514
rs50699338	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77428090	TAAAATCTAGAGACC[C/T]TCGGCTCTCCATGAA	78514
rs50705682	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77505378	CTAGAGAACTAAGAG[C/T]TCTGACCAGGGTATG	78514
rs50706171	snp	G/T	0.152778	0.230321	intron-variant	Arhgap10	Mm_Celera	8:77414004	CAATCTGAACACTGA[G/T]GATCTGAAAATAATC	78514
rs50708066	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77483597	TTGCAGGATCGGGAT[C/T]AGGATGTCAAATCTA	78514
rs50711648	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77373274	GTTCCTTGACCCTTC[A/T]CTCTTCACCTCAGTG	78514
rs50714218	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77276512	AATTTTTAATGCTCT[C/T]TGGGTGAATTATAAA	78514
rs50714238	snp	A/G			downstream-variant-500B	Arhgap10	Mm_Celera	8:77250130	GCTGGTCATCAGCAT[A/G]ACTATAGCTCACCCA	78514
rs50731170	snp	C/T	0.46875	0.121031	intron-variant	Arhgap10	Mm_Celera	8:77482766	AATGTGACCTAGAGC[C/T]CTGTTTCTCAGCACT	78514
rs50765758	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77507324	CCCTGCTCCCCACAC[A/G]CTCATCATACCTACA	78514
rs50766540	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77427542	AGCATCTCTGTGCAT[G/T]TACATCCATTACAGT	78514
rs50770477	snp	A/G	0.297521	0.245442	intron-variant	Arhgap10	Mm_Celera	8:77512366	CTAATTATTTTCCCA[A/G]CCAGCCTACATTCCT	78514
rs50774655	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77404845	TGGAACTCACTCTGT[A/T]GACCAGGCTGGCCTT	78514
rs50776304	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77254273	AACTGGAATTCGTAG[C/T]CCAAGTCCATGGTCT	78514
rs50789805	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77424856	GACACTCAGTATTGA[A/C]TATTGAGGTATTGAG	78514
rs50799487	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77298926	TTCACAATAGTCACA[A/T]ATAATATAAAATACC	78514
rs50804672	snp	C/G	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77464300	GGTCTGTGGAGTGTG[C/G]ATTCTGCCTAATGGA	78514
rs50812230	snp	C/T	0.260355	0.249785	intron-variant	Arhgap10	GRCm38.p3	8:77505801	CACACTTGCCACAAA[C/T]CTAAGACAACCAAAT	78514
rs50813944	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77253546	TGTAAACTCTCCATC[C/T]ATGACAAATGGCCTT	78514
rs50818922	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77275845	GCTGTTCCATGCCGC[A/G]TGATGTCACTGTCCT	78514
rs50818947	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77480261	GGCCTGCAGGCTCCC[C/T]AGCTTTGTCTACTCC	78514
rs50820850	snp	A/C	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77400808	ATTTTTAAGACAACT[A/C]TTCTGCCTCATGTTG	78514
rs50821310	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77408919	TTCTTAATCCTCTCC[A/G]TTGGAAGACTTACTA	78514
rs50844125	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77450818	AAAGCGGACCCCCTG[C/T]ATTTCTTACCTATGC	78514
rs50844208	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77511579	TCATGTGGATGGACA[A/G]ACAGGCTACACTGCT	78514
rs50851456	snp	C/T	0.260355	0.249785	intron-variant	Arhgap10	GRCm38.p3	8:77490241	GCCAGCTCCACCCTA[C/T]GCCTGCCTACACCTG	78514
rs50856222	snp	A/C	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77405137	AGCGAGGTACCAAGT[A/C]ACACTAAGGGAGACA	78514
rs50867794	snp	A/G	0.48	0.0979796	intron-variant	Arhgap10	Mm_Celera	8:77451811	ATGTGAAGAGGCTCC[A/G]CCATCAGCGGTCAGG	78514
rs50870600	snp	A/G	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77400413	AAGACACTAAATCTC[A/G]ACTTTTCCTCCAGAG	78514
rs50870954	snp	C/T	0.277778	0.248452	intron-variant	Arhgap10	Mm_Celera	8:77388619	CAAGCCAGCTGAGTG[C/T]ATCTGAACTAGAGCT	78514
rs50893876	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77320749	TCAAGTTCCCACCTA[A/C]GGGATCTGTAAGAAA	78514
rs50896148	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77253663	GTCTCCTTCCCAACT[C/T]TTAATGAAAACACCT	78514
rs50896158	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77328699	CACCATAAATGGGTA[A/G]CTTGGTCAACAGCTG	78514
rs50904198	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77313696	TCACAAAACAGAGTG[G/T]CCACACAGGCTGCTC	78514
rs50907911	snp	C/T	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77408588	GAGCTGGGTCCGAGG[C/T]AGCATGGGCACAGGC	78514
rs50908326	snp	C/T	0.495868	0.0452663	intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77485072	AATTACAGTCACAGC[C/T]CTTCCCCTCAGCTTC	78514
rs50910085	snp	C/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77388222	CAAAGTAGAAACCAT[C/T]ACAGTATATCCACCG	78514
rs50911108	snp	C/T	0.375	0.216506	intron-variant	Arhgap10	GRCm38.p3	8:77460708	CCACAATCCAGAGGT[C/T]AGAACAAGCACTCTG	78514
rs50920476	snp	A/G	0.197531	0.244432	intron-variant	Arhgap10	Mm_Celera	8:77454410	TTCCAGCGGTGAAGT[A/G]GACACAGTCGACAGC	78514
rs50930525	snp	A/C	0.132653	0.220748	intron-variant	Arhgap10	Mm_Celera	8:77419921	CATCAGCTTCAGAGC[A/C]ATGTGTTACACCAAA	78514
rs50937883	snp	C/T	0.5	0	intron-variant	Arhgap10	Mm_Celera	8:77460613	TTGCACAAGCATGCC[C/T]GTGGTGCACCAGCCC	78514
rs50943994	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77388521	ACAGGAGTGCCAATA[C/T]AGTTCCAAGATGCGT	78514
rs50946009	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77513779	ACTGCTGCTGACACC[A/G]TTTCCCCTACAGTTA	78514
rs50955374	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77480390	CCAGTAAACATGAAC[A/G]GACTAACCTTAATTT	78514
rs50967940	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77348120	CCATTAACAGGCACT[C/T]CCATAATGTAACATA	78514
rs50971948	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77371002	TCAAGCACTTGTTTA[A/G]TTTTTAACTGTGCTA	78514
rs50984830	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77456830	GAAAATGTGGTACAT[C/T]TACACAATGGAGTAC	78514
rs50988472	snp	A/C	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77415790	GAATCAAATAACTTC[A/C]AATGGTACCTGAGGT	78514
rs50994184	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77506446	ATTGAATTCAGATGT[C/T]CCCACTCAAAATGAC	78514
rs50996740	snp	A/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77469763	TTCACGTGTAATAAA[A/T]AAATATGTACTTCAC	78514
rs51013204	snp	A/C			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503781	AGGCAGGAGCTACCC[A/C]TTACTCCATCGCCCA	78514
rs51014386	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77255415	TGAGGAGCATGTCTC[C/T]CAAGTGGCAACAGTA	78514
rs51030777	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77347327	TGAAGAAATTTATTA[A/G]TAAGAAGAACATATT	78514
rs51033557	snp	C/T	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77398435	CAGTGACCCTTGACA[C/T]GGGAAACCGGTTCCT	78514
rs51056774	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77488816	TACATCGGTTCCCTA[A/C]TAAGTAAGATGGGTA	78514
rs51059745	snp	A/G	0.152778	0.230321	intron-variant	Arhgap10	Mm_Celera	8:77396352	GAAGGGTGTCCATGC[A/G]TTATAGTCAACAACG	78514
rs51060695	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77254029	GACCACATGGGGACT[C/T]TGGCCTCCTGAAAAC	78514
rs51068097	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77287676	AGCCGGGCGTGGTGG[C/T]GCACACCTTTAATCC	78514
rs51080410	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77347021	AGGGTCCAGATTCAC[A/G]GGGCAAGAAGGGCTG	78514
rs51098716	snp	A/G	0.408163	0.193609	intron-variant	Arhgap10	Mm_Celera	8:77478013	CACAGGCCTGCGTCC[A/G]TCGACACCAACCGTG	78514
rs51099082	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77295445	GTATGTAGTCCTATA[A/T]TAGGTGAGCATTTAA	78514
rs51106381	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77403943	CTATGAAAAATGCAC[C/T]TCTGAATTACCATTC	78514
rs51119279	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77409167	TCGCCAACCTCATGA[C/T]GAGAACATACGCTCA	78514
rs51120168	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77387874	CTCCTCTTCCATCTT[C/T]AGATCATGCCCCCCC	78514
rs51121963	snp	C/T			downstream-variant-500B	Arhgap10	Mm_Celera	8:77250107	GCCCAAAGAAGCCAG[C/T]CAGGAGGGCTGGTCA	78514
rs51123589	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77422505	AGGAGATCAATCTCA[C/T]GCAATATTACTAAAA	78514
rs51125355	snp	A/C	0.336735	0.234472	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485770	GGCTATACACCCAGG[A/C]ATGACATTTTTCAAC	78514
rs51131201	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77331780	ACACAGGAGTGCTTC[C/T]GAGGGGCTTTTCATC	78514
rs51131427	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77396856	ATCAGAAACAGGGAA[C/T]GAGCTGTCCAGGCTT	78514
rs51132410	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77255230	AGAGAGAATCAGCAC[A/G]CCAAGCAGGAGGTTT	78514
rs51134497	snp	A/T	0.277778	0.248452	intron-variant	Arhgap10	Mm_Celera	8:77507929	ACACAGTCAGTAAAG[A/T]AAAGCTGACCTTATC	78514
rs51147655	snp	C/T	0.142012	0.225474	intron-variant	Arhgap10	Mm_Celera	8:77472831	TGGTGAGACAGGAGA[C/T]GGAGACAGGAGACTC	78514
rs51157111	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77423282	CTGGAAGGAGCTCTG[A/G]TCTGTTATGCATTGT	78514
rs51162803	snp	C/G	0.375	0.216506	intron-variant	Arhgap10	Mm_Celera	8:77457761	TAAGCCACGTGCCAT[C/G]CACATGCATTATACC	78514
rs51206440	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77482770	TGACCTAGAGCTCTG[C/T]TTCTCAGCACTTGGC	78514
rs51214183	snp	A/G	0.35503	0.226867	intron-variant	Arhgap10	Mm_Celera	8:77413804	GAGTGTAAAACAGTC[A/G]ATCGAGAGGGTGAGC	78514
rs51218578	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77467096	AGGACCTACTTTGGA[A/G]CAATGTACTATAGCA	78514
rs51220593	snp	A/C	0.244898	0.249948	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493598	TTTGTTGGGCTAAAC[A/C]CACCAAGACATGCTG	78514
rs51222547	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77288365	CTGAGAAAGGATTGT[G/T]ACTCCAGACTGGATT	78514
rs51230797	snp	C/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77496705	TAGGCACAGCTCAGT[C/G]CTTCCATGATACTTT	78514
rs51250173	snp	A/G			downstream-variant-500B	Arhgap10	Mm_Celera	8:77250134	GTCATCAGCATAACT[A/G]TAGCTCACCCATTCA	78514
rs51271243	snp	A/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77388817	GTCTGACTATATAAA[A/T]TAAAGGTTTCATTCA	78514
rs51271479	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77374789	AGGCTCACATGCAGA[C/T]GGACAGTTGTTCCTA	78514
rs51286339	snp	C/T	0.35503	0.226867	intron-variant	Arhgap10	Mm_Celera	8:77463659	CCTTTGCTTTAAGTG[C/T]GCAGAGTTGGAGGGC	78514
rs51286711	snp	C/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77496329	TTACAAAGTCACACC[C/T]GCAAAGACTAAAGCC	78514
rs51287692	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77251405	AGCACTTTACTTGCG[A/G]CCTAGAATGCCCTTG	78514
rs51288748	snp	A/G	0.42	0.183303	intron-variant	Arhgap10	Mm_Celera	8:77511178	TAATCTAAATGCTTT[A/G]CCTATATCAAGTCAC	78514
rs51297803	snp	C/G/T	0.152778	0.230321	intron-variant	Arhgap10	GRCm38.p3	8:77495917	ACCCCTTCAGAATAT[C/G/T]CGGAGGCAGGACACA	78514
rs51299274	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77444118	TGCATCTTTTCTAAC[C/T]CTCTAGTCCAAACCC	78514
rs51303801	snp	A/G			intron-variant, utr-variant-5-prime	Arhgap10	GRCm38.p3	8:77483885	TCCTTCTCTCCGAAG[A/G]ACAGGCGAGTGACTT	78514
rs51309575	snp	G/T	0.46875	0.121031	intron-variant	Arhgap10	Mm_Celera	8:77483596	CTTGCAGGATCGGGA[G/T]CAGGATGTCAAATCT	78514
rs51311833	snp	A/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77398786	GTCTTAAAAAATGTA[A/T]AGGCCTTCATGACTT	78514
rs51314753	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77495796	TTCAGCTTCACGATC[C/T]GTATGGCTTGAAGTG	78514
rs51317183	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77443486	CCCACAGACAAGCCT[A/G]AAGTCGGGTCTCCTG	78514
rs51353062	snp	A/T	0.142012	0.225474	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494031	TACACCATGTGACAG[A/T]TAAAAAGGAGGACGC	78514
rs51357973	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77423153	AGGCAGAATGGATAG[A/G]GGACTCTGAACTGTA	78514
rs51369063	snp	C/T	0.152778	0.230321	intron-variant	Arhgap10	Mm_Celera	8:77401331	CTTGTCTCTCTGAAA[C/T]CCTGGTTGTCAATGC	78514
rs51373955	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77275962	ACTTCACTAAGAAGC[A/T]CACAGACTAACTCCA	78514
rs51378461	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77449795	ATGTGGATCAGTTTC[C/T]CCATTCATAAAACAG	78514
rs51383094	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77451092	CCCACAGCCCAGCAC[A/G]GAGAAGCCACCATCC	78514
rs51404286	snp	A/G/T	0.277778	0.248452	intron-variant	Arhgap10	GRCm38.p3	8:77504367	CAGCAAAAGCCAGCC[A/G/T]CGTGTTGTCAGTGGC	78514
rs51409501	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77353354	TGGTCAGCGTGAATG[A/T]GTGTGTGTGCGCAGG	78514
rs51412720	snp	C/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77409096	ACTGAAAACTAAATG[C/T]TTCGAAGTTATTTTG	78514
rs51413091	snp	C/G	0.142012	0.225474	intron-variant	Arhgap10	Mm_Celera	8:77420366	AATAGGTGGTCTGTA[C/G]AGAAAATTATGAACA	78514
rs51435837	snp	A/C	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77455511	ATAAGTGAAGTTCCA[A/C]CATCCTGAACTTGAA	78514
rs51440850	snp	C/T	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77488119	GACAAGCTCATAGAC[C/T]CAGAATCGCAATGTG	78514
rs51441396	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77504630	GATCCATCATCACGG[G/T]GCGAGCATGGCACAC	78514
rs51464713	snp	C/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77321959	TGGCTACAAAGAAAA[C/G/T]GCTAATGTGTTTTTG	78514
rs51465162	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77438888	TTAAACTGACTCTTA[A/G]CCCTGTTAAAGAAAC	78514
rs51467219	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77346544	ATCTTCGTCCCTCTA[C/T]TTTTCAGGTACCTCT	78514
rs51479566	snp	A/C	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77408770	CAGGGTGCTTAAGGG[A/C]ACGTATTTTTATACA	78514
rs51486804	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77403967	ACCATTCAAATGTTT[C/T]GTGTGGACATATGTG	78514
rs51502126	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77314415	CTTTCTTGGTGCTTG[A/G]CTCCCTGGCTTCATT	78514
rs51504992	snp	A/C	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77499644	GAACCCTCTATATAA[A/C]AGCAGCTCTCAACCC	78514
rs51507189	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77396812	TAAACACGAAAGCAA[C/T]ACAATGAATTTCCTA	78514
rs51509830	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77427308	CAAATATCCCAGCTT[C/T]TGCCTGCAGAGATGA	78514
rs51525128	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77427753	CACTACACCGGCAGC[C/T]CCAGTACTGCCACAG	78514
rs51531271	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77288372	AGGATTGTGACTCCA[G/T]ACTGGATTGCTGCAG	78514
rs51531326	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77474318	GATCAGAGAAGCATC[A/G]GACAGTGGAGGGGAT	78514
rs51537967	snp	A/G	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77499600	CATGCTCCTGCCTCC[A/G]TGACAGTCTGTCCAA	78514
rs51547361	snp	C/T	0.297521	0.245442	intron-variant	Arhgap10	Mm_Celera	8:77513759	GGCAGGTAACAATGG[C/T]TAGGACTGCTGCTGA	78514
rs51552866	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77427818	AGCACTGCACAGATG[G/T]TGTTGTGTCTTGCTC	78514
rs51560964	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77369993	GGGACCAAGGAAAAG[A/G]TGCATGAAAGTGGAT	78514
rs51571937	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77251778	GATGGGGGATTGTGT[C/T]TATCTACAGAACAAC	78514
rs51577671	snp	A/C	0.32	0.24	intron-variant	Arhgap10	GRCm38.p3	8:77489596	TGTAACTTCTAGGTG[A/C]TCTCATGCTACAACA	78514
rs51602299	snp	A/G	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77413302	CTCCTGGAGCACATC[A/G]CTAGATAGCATGTGG	78514
rs51603751	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77378362	ATGCCTTCCAAGGTC[C/T]ATGTATTATTGGAGG	78514
rs51606926	snp	A/C	0.231111	0.249285	intron-variant	Arhgap10	Mm_Celera	8:77507794	ATCACTGGAACTCTA[A/C]CTCTCGTGTCCAGTC	78514
rs51619195	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77346559	CTTTTCAGGTACCTC[C/T]CACACAGCTTCATGC	78514
rs51626736	snp	C/T	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77500294	AACTGGAAGGGGACA[C/T]GGTGTGAACCTCGAG	78514
rs51634214	snp	C/T	0.277778	0.248452	intron-variant	Arhgap10	GRCm38.p3	8:77458142	ACCAGTGAGTTAAGC[C/T]GATGGTTTTGAGAGG	78514
rs51645842	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77474920	ACCCCCAACAAAAGC[A/G]TAAGGGCCTGAGTTC	78514
rs51653715	snp	A/C	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77461289	TGCAAGACGCAGATA[A/C]GGTCATGGTTTAACA	78514
rs51655752	snp	C/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77470579	CAGCCGGCTCTGCAT[C/T]TCTGGCTAACAGAGT	78514
rs51656405	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77402772	CTAAGCTTGAAAAGA[A/G]CTCCGACCTGAGATG	78514
rs51656686	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77253805	TCTGAGATTCCTACG[A/T]TCAGAATACATCTGG	78514
rs51673792	snp	A/G	0.444444	0.157135	intron-variant	Arhgap10	GRCm38.p3	8:77402261	TATCTTATGTGTAGC[A/G]TGACCAAAGCCAGTC	78514
rs51677467	snp	A/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77398630	CTGAAACAGCCAAAA[A/T]GTTCCAACTCTAACA	78514
rs51689900	snp	C/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77471835	CCACAAAGAATGAAA[C/T]AGACTGAAGAGCGGA	78514
rs51692879	snp	A/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77395716	CAATCTTCCTTCTTA[A/T]GACTGAATGATACTT	78514
rs51699207	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77345423	AATTAATCATAGTCC[A/G]TTTCACAAGCATAAG	78514
rs51706496	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77255432	AAGTGGCAACAGTAA[G/T]CAAAGCTCAGGCTTC	78514
rs51707518	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77408743	CCCTTGCCACAGCAC[C/T]GCCAACTTTGGCAGG	78514
rs51711985	snp	C/T	0.277778	0.248452	intron-variant	Arhgap10	Mm_Celera	8:77412131	ACCTGGACAAAGCAA[C/T]GGTACAATGATTATT	78514
rs51720006	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77372502	TAGTCTATAAATATA[A/T]CAACTCAACTCTCTT	78514
rs51732194	snp	A/G	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77501317	GAGCCAGCCCTGGCC[A/G]CCTCTTCCCAAGTCC	78514
rs51738712	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77255331	AGACAGCTGGCCACC[C/T]ACACTACAGTGCATC	78514
rs51748446	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77320455	CCAGCGATATTGGGC[C/T]TGGTCAGAGGCCTGG	78514
rs51757220	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77409255	CCACACACCACCCAC[A/G]CTCTCCTTCATTACT	78514
rs51759587	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77389066	AGATGTTGTGATCTT[A/G]CAAAAGTAAACCTCT	78514
rs51761755	snp	C/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77398477	GGTTTTTGTTCACTG[C/T]CTTTTTAAATACCGT	78514
rs51763670	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77498569	GGGACTTAGAAAGCA[A/G]CTTACCCCTGGGTGA	78514
rs51769147	snp	A/C	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77498353	TGGAACCAAGTGAGG[A/C]CCACAGAAACAATTC	78514
rs51801067	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	GRCm38.p3	8:77515596	CTTGAGGGGAAGAGT[A/G]TAAAGTTAAGGATAA	78514
rs51802129	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77455648	CTGTAAGATAGTACT[G/T]CAGGCGAGCTGGTAG	78514
rs51809126	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77434991	GGGGTCAGGGGGAGC[A/G]GATTCCAGCCTGAAG	78514
rs51810584	snp	C/T	0.32	0.24	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484051	TTCTGACAGGCTCTT[C/T]CCTCCTAGGAAGGTC	78514
rs51813135	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77321950	TGTGTGAGTTGGCTA[C/G]AAAGAAAATGCTAAT	78514
rs51816862	snp	A/C	0.345679	0.230967	intron-variant	Arhgap10	GRCm38.p3	8:77505823	CAACCAAATGAACTG[A/C]AACTCAGTATCTCCG	78514
rs51818781	snp	A/C	0.32	0.24	intron-variant	Arhgap10	GRCm38.p3	8:77488739	CTAGAAGCTGACATT[A/C]AGGACCTAGATTCAA	78514
rs51820891	snp	A/G	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77408550	ATCAAGGCAGATAAC[A/G]CTCACAAGGACAGAG	78514
rs51828416	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77424753	TTATGCTTTTGTTGG[A/G]AAGTCATAATCCTAT	78514
rs51831113	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77398746	GAAAGGAGAATATGA[C/T]TAATAGATGCAATAG	78514
rs51833435	snp	G/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77467017	TCTCTCCTCTGAGAA[G/T]CTCCTGTCATCATCC	78514
rs51833708	snp	C/T	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77415611	TATTTGTAAAATATG[C/T]CGTATTTCTTTATGT	78514
rs51845677	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77324019	ACCCCTTCCATAGGA[A/G]CATGCTCTCCCTCTC	78514
rs51848110	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77489806	TTCACCAAGAGTCCT[C/T]GCTTACCTCGCCTGG	78514
rs51850010	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77251970	GTACACTGATGGTTC[A/C]TTCTGACTGTTCTTC	78514
rs51853153	snp	A/G	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77398090	GTAAATGGTTACAAG[A/G]CCCAATGGTGGAAGC	78514
rs51855165	snp	C/T	0.35503	0.226867	intron-variant	Arhgap10	Mm_Celera	8:77413222	GCAGAAAGGTGCTGG[C/T]GACATAGTCCCTCCT	78514
rs51859228	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77507087	GAGTGCTTGTTATAC[A/G]ATCATGAGAAGCTGA	78514
rs51861395	snp	A/G	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77408898	ACCTGAAAAAAGAAA[A/G]GTTTGTTCTTAATCC	78514
rs51866211	snp	A/G	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77487144	AAATGCTGAAACCAA[A/G]GCCAAAAGATAAAAA	78514
rs51877960	snp	A/C			downstream-variant-500B	Arhgap10	Mm_Celera	8:77250028	AGCCCAGCTTTATCA[A/C]GATGGGCAAAGGTAA	78514
rs51888947	snp	C/T	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77411861	CTACGGATTAAACAG[C/T]GGGCGCACACCATCC	78514
rs51891405	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77448158	TGCCAAAGGAAGTTG[C/T]GCGCATGCGCGCGCG	78514
rs51900507	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77429202	TCACTCTTCAAACAT[C/T]CCAGGAAGCAGAGTC	78514
rs51914188	snp	A/G	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77404342	ACTATCGGAAACACG[A/G]GAGCAAGGATCCTGA	78514
rs51932404	snp	A/C	0.391111	0.206368	intron-variant	Arhgap10	GRCm38.p3	8:77402312	AAGAGTCCACTTACA[A/C]ATCATTTCTTGGGCT	78514
rs51938318	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77428082	CAGACATATAAAATC[A/T]AGAGACCCTCGGCTC	78514
rs51947793	snp	C/T	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77403207	CAGGCAGCATCGCGG[C/T]GAAGAACCTGGATGT	78514
rs51964669	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77263814	CCCCTGCAGACATGG[A/G]ACAAGAAGTACTAAT	78514
rs51965956	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77336531	TGGATTCCTAGCAAT[C/T]CCCACAACTACATGA	78514
rs51982973	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77374617	GCCCACGCTTACCCT[A/G]AGGGGCAGTTATATG	78514
rs51990848	snp	C/T	0.391111	0.206368	intron-variant	Arhgap10	Mm_Celera	8:77500802	CTCCAGATACCAGCT[C/T]ACGCTGCAAATACCT	78514
rs51992686	snp	A/C/G	0.5	0	intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77484916	TCAGTTTAAAAACTG[A/C/G]CGTGCTTCTGCTCCA	78514
rs51994066	snp	C/T	0.32	0.24	intron-variant	Arhgap10	Mm_Celera	8:77463346	GGATACAATCATCCA[C/T]TTTATAAAGCTCTGT	78514
rs51997557	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77254286	AGCCCAAGTCCATGG[C/T]CTGATAGTACGAAGA	78514
rs51999596	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77425056	CAGGCGGGTCACACC[A/G]ACAGGAACTCCAGCT	78514
rs52000397	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77275953	GGGATCTGGACTTCA[C/T]TAAGAAGCTCACAGA	78514
rs52008395	snp	C/T	0.244898	0.249948	intron-variant	Arhgap10	Mm_Celera	8:77413764	CAGTGTGTGTCCTTA[C/T]TGAGATTGATATCCG	78514
rs52012196	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77279203	GGAGAAACTCAGTCT[A/G]GACATTAGGGCCAAC	78514
rs52017986	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77353189	GCCATATCCAAAGCG[A/G]AATGCAGTGAGTGCT	78514
rs52037094	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77423467	CTGTGGGATAAGGGA[C/T]CATGAGAACTGACCA	78514
rs52045903	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77252128	TAGGTCCTAAATATT[C/G]GACACTGCAACCATG	78514
rs52103298	snp	A/C/G	0.244898	0.249948	intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77493376	TCCTCCTTCACTGGC[A/C/G]TACAGGAACACAACA	78514
rs52104208	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77305456	ATATAGTACAATAAT[A/T]AATGTAACTGTGTTA	78514
rs52110709	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77491362	GCAGTGGGTCCCAGT[A/G]CATTTACTCCAAGGT	78514
rs52117905	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77452051	CTCGGCATGACTCAT[C/T]CTGTCATAAGAGTTG	78514
rs52121047	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77445359	TACAATATTTAGCAT[A/T]TGTAGCTGCTTGTAT	78514
rs52128777	snp	A/G	0.142012	0.225474	intron-variant	Arhgap10	Mm_Celera	8:77461493	CCAAAACCTAATAAC[A/G]GTTAAAAATGAGCCC	78514
rs52134654	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77480440	TTATTTTTGGTTTTT[C/T]GAGACAGGGTTTCTC	78514
rs52135893	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77287950	agaaagaaaaagaaa[A/T]gCCATTCTCAGCAGC	78514
rs52143117	snp	A/G	0.497778	0.0332592	intron-variant	Arhgap10	GRCm38.p3	8:77458076	TATCTATGCCAACAC[A/G]TATTATCATTCCATT	78514
rs52144191	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77482511	AGAGAGGAGGGTGGA[A/G]AGAGAGAGGGAGGGA	78514
rs52147369	snp	C/T	0.42	0.183303	intron-variant	Arhgap10	Mm_Celera	8:77472751	GAATATATATTACTG[C/T]TCAAGGACTTGAGCT	78514
rs52149955	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77483210	CCACATGTGCCCCAG[A/G]TATGTGCATGCCTTA	78514
rs52150641	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77472573	AAATAAATCTTTTTT[A/T]AAAAGATATATGTGT	78514
rs52178133	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77511742	GGTCTACAAAGTGAG[C/T]TCCAGGGCAGCCAGG	78514
rs52180044	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77499005	GCCCCCTGCCCGCTG[C/T]CCGCTGCCCGCTGCC	78514
rs52204644	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77483234	TGCCTTacacacaca[A/C]acacacacacacaca	78514
rs52225182	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77261092	AGAGAGAGAGAGAGA[C/G]AGACAGACAGACAGA	78514
rs52229181	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77320285	TAAATAAATAAATAA[A/G]TAAAAGGGAGTCTAT	78514
rs52240152	snp	A/G	0.391111	0.206368	intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77495185	CAACACTACAATTGG[A/G]TGCCCTGTAGGTTGG	78514
rs52253619	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77414911	ACACACACACACACA[A/C]ACACACACAAACACA	78514
rs52261669	snp	A/G	0.495868	0.0452663	intron-variant	Arhgap10	GRCm38.p3	8:77457936	TTGATGACCACAAAT[A/G]TAGTGGGCACACTAT	78514
rs52268675	snp	C/T	0.444444	0.157135	intron-variant	Arhgap10	Mm_Celera	8:77416608	AAAACCAGAAAAGTA[C/T]AGTTCCCAAGACAGA	78514
rs52317936	snp	G/T	0.48	0.0979796	intron-variant	Arhgap10	Mm_Celera	8:77482403	ACTTTACAGGACACT[G/T]CAAAAGGAGAGGGGG	78514
rs52329655	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77287970	TTCTCAGCAGCAAAA[G/T]TGGAGGTGCCCGCAC	78514
rs52341666	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77261076	AGAGAGAGAGAGAGA[C/G]AGAGAGAGAGAGAGA	78514
rs52343070	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77452090	TCTGCTAACAACAGC[A/C]Caaaaaaaaaaaaaa	78514
rs52346566	snp	A/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77466283	ATGCACTGGCACGTG[A/G]GGAGAAGATGGAGGA	78514
rs52352685	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77404805	TTTTCTGAGACAGGG[A/T]TTCTCTGTATAGCCC	78514
rs52356615	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77511749	AAAGTGAGCTCCAGG[A/G]CAGCCAGGGCTACAC	78514
rs52357379	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77261054	ACACACACACACAGA[C/G]AGAGAGAGAGAGAGA	78514
rs52357746	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77511851	ACTGGCCTGGAACTC[A/T]CTCTCTCTCTCTCTC	78514
rs52397580	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77498985	TGCCTCGCCCCCTGC[C/T]CCCTGCCCCCTGCCC	78514
rs52400124	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77458060	TATCTATCTATCTAT[A/C]TATCTATGCCAACAC	78514
rs52401679	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77498882	TCTCTATGTAGCCCT[G/T]GTTGTCCTAGCACTC	78514
rs52416247	snp	C/G	0.124444	0.216185	intron-variant	Arhgap10	Mm_Celera	8:77406899	AGTTCTTAAAGGTCC[C/G]TAGGCAGCAGTAATA	78514
rs52427203	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77407436	TAGATAGAGATGGAT[A/G]GATAGATAATTAGAT	78514
rs52444730	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77457601	TTTGGGATAGCATTG[A/G]AAATGTAAATGAAAT	78514
rs52450693	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77377822	ACACACACAGACACA[C/G]ACACACACACACACA	78514
rs52463752	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77417871	CACACACATGCAAGC[A/G]TGCACACGTGAGGGC	78514
rs52464581	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77458039	CTACCTACCTACCTA[C/T]CTATCTATCTATCTA	78514
rs52473876	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77377816	AAGTACACACACACA[C/G]ACACAGACACACACA	78514
rs52509961	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77458011	CTATCTATCTATCTA[C/T]CTACCTACCTACCTA	78514
rs52529722	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77287936	agggaaagagaaaga[A/G]aaagaaaaagaaaag	78514
rs52536465	snp	A/C	0.260355	0.249785	intron-variant	Arhgap10	Mm_Celera	8:77421098	TACACACGATGAAAT[A/C]TAACAAAAGGGGACA	78514
rs52539008	snp	A/G	0.297521	0.245442	intron-variant	Arhgap10	Mm_Celera	8:77511529	GGCAGGCAGGCTACG[A/G]AGCTGGACCCAGGTC	78514
rs52539840	snp	A/G	0.35503	0.226867	intron-variant	Arhgap10	Mm_Celera	8:77389183	ATCTCAGAACCATAA[A/G]ACAAGAAACCACATC	78514
rs52542815	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77489207	ACCTCTATATATATA[C/T]ACACACAGACATTCA	78514
rs52543675	snp	A/G	0.396694	0.202437	intron-variant	Arhgap10	Mm_Celera	8:77466254	ACACATACCACGTGA[A/G]CACATGCAGACACAT	78514
rs52555684	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77320223	AGGGAGTCTATGACA[G/T]CCAGGGTTACACAGA	78514
rs52569075	snp	A/C	0.336735	0.234472	intron-variant	Arhgap10	Mm_Celera	8:77472089	TGTTATGATTTCACA[A/C]CCCAAAAATAATCGT	78514
rs52583285	snp	A/C	0.132653	0.220748	intron-variant	Arhgap10	Mm_Celera	8:77514145	AACCATCTCTCTCCG[A/C]TTACATCAGGCTCCC	78514
rs107642480	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77482451	GGGAGGGGAGAGGGG[A/G]AAAGAAATGAAAAGG	78514
rs107658319	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77301263	CGAGAAAATCCGGGA[A/C]GAAAAAACCCGGGAC	78514
rs107664031	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77414921	ACACAAACACACACA[A/C]ACACACACACACACA	78514
rs107727434	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77504670	TGGTCACACAGCAAG[A/C]ATGGCACACTGGCCA	78514
rs107804931	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77417877	CATGCAAGCGTGCAC[A/G]CGTGAGGGCACACGC	78514
rs107843202	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77301275	GGAAGAAAAAACCCG[A/G]GACAAGAAAACTCGG	78514
rs107855865	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77371214	GCACACGGCCAGGAA[A/G]CCCAACAACCTGACT	78514
rs107865356	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77301110	GCAATGGGGGGTTTG[A/G]GGCTTGCACTCTTGC	78514
rs107894488	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77301266	GAAAATCCGGGAAGA[A/G]AAAACCCGGGACAAG	78514
rs107975737	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77364195	TATTCTAGCAAAACA[C/T]GCAAGTGACAAAGGG	78514
rs108086546	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77364186	AAGTGAATATATTCT[A/T]GCAAAACATGCAAGT	78514
rs108089222	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77301248	CGAGAAAATCCGGGA[A/C]GAGAAAATCCGGGAA	78514
rs108203836	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77364444	AATTCTTACATAGCA[A/T]GGCCAAAATTACAGA	78514
rs108222531	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77301203	GCCGGTCGTGAGAAC[A/G]TGTGTAAGAGTTGGT	78514
rs108309789	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77301175	AAGATTCTGGTTTGT[A/T]GTGTCTTTCCTGGCC	78514
rs108354163	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77301256	TCCGGGACGAGAAAA[C/T]CCGGGAAGAAAAAAC	78514
rs108376173	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77300807	CGCCCCCACATTCGC[A/C]GTCACAAGATGGCGC	78514
rs108392714	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77341899	CTCAGGAAAAAAAAT[A/T]AAAATAAAAAATACG	78514
rs108395420	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77301181	CTGGTTTGTAGTGTC[C/T]TTCCTGGCCGGTCGT	78514
rs108429370	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77301204	CCGGTCGTGAGAACG[C/T]GTGTAAGAGTTGGTG	78514
rs108458073	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77364164	CAGAAAATGGAAACA[A/G]CCACATAAGTGAATA	78514
rs108495968	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77298133	CCATGCTTCCTGCTA[C/T]GACGATAATAGACTA	78514
rs108503778	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77374406	CTCACAAAGCACCTT[C/G]TCACACAAGCCACCC	78514
rs108504565	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77364207	ACATGCAAGTGACAA[A/T]GGGCAACTTTTCCTG	78514
rs108586633	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77301273	CGGGAAGAAAAAACC[C/T]GGGACAAGAAAACTC	78514
rs108658547	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77374886	GTTGTCCCTACTGCA[C/G]CTGAGGCTCACATGT	78514
rs108751659	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77371218	ACGGCCAGGAAGCCC[A/G]ACAACCTGACTTCAG	78514
rs108797974	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77363899	CAGAGTCACTTTGAC[C/T]GACTGACTCCAAAAT	78514
rs108807363	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77304537	CTCTGGCGCTCTGGC[G/T]CTCTGGCGCTCTGGC	78514
rs108844814	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77252414	CCCACAGTGACCTTG[A/C]CCCTGACCTTGTTAC	78514
rs211697859	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77496755	TCATAATGGGACTAA[A/G]TGTTTGTTTGAAGCA	78514
rs211702371	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77488837	AAGATGGGTAGCAGA[A/G]CAGTGGTATGGACCA	78514
rs211709135	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77364754	CAGATGACAGTCTGC[A/G]AAACTAAAAATGAGC	78514
rs211714904	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77271892	GCCTGGGCTAGCAAC[-/T]CTTCACTGGCAATGA	78514
rs211742498	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77320177	GAGGCCGAGGCAGAT[A/G]GATCTCTGTGAAGGC	78514
rs211744059	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77410281	TTTCTGGACAAAGTG[A/T]AAGGTACATAGACAG	78514
rs211745421	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77452855	CATGGCAGCTCACAA[A/C]GGTCTGTAACTCCAG	78514
rs211750034	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77265136	AAAAATTATTAGAAG[A/C]GACTACGCCCTGTAG	78514
rs211760605	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77405400	GTTGGGGTGGGGAGA[A/T]GCACACAGAAATGTG	78514
rs211770648	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77365355	GAGACCCAAAGATGA[C/G]CACATGCAGCAGAGT	78514
rs211772129	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77415235	TAGTGGGGAATCCCA[A/G]GCTGATCTATTGTAC	78514
rs211789766	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77458896	CAAAGAGCAACAGAG[A/C]AAGGCAGCCAGGGCC	78514
rs211794746	in-del	-/TGTGTGTT			intron-variant	Arhgap10	Mm_Celera	8:77443968	AACTCAGAAAGTGTG[-/TGTGTGTT]TGTGTGTGTGTGTGT	78514
rs211803405	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77405955	CAACACAAAAAAGCA[A/G]GAACTCTGAAAATGA	78514
rs211819972	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77501754	TCACTGCAACTAGAC[C/T]ACCAACCCTGCCCAG	78514
rs211830235	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77414729	AGCCAGGGCTACACA[A/G]AGAATACAGGGCTAC	78514
rs211830785	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77421406	AAGTCACGGCTTCCC[A/G]GTCAGGGCTTCTGCT	78514
rs211837355	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77257974	TGGCTGGTTTCCTGT[A/G]TCAACTTGACACAAG	78514
rs211837459	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77265593	AGAAGAACCCATCAG[A/G]GGCTGCCCTGGAGAC	78514
rs211838609	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77358985	ACCATTGAGGCAAAG[A/G]GATGTTGAATGGCAG	78514
rs211838611	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77345609	TCCTTCGAACACCCT[-/C]TCTCTCTCCTTGCAA	78514
rs211863152	snp	A/C/T			intron-variant	Arhgap10	GRCm38.p3	8:77464322	CCTAATGGAGAGCCC[A/C/T]GAGCGATGCTGTTAC	78514
rs211864302	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77315178	GATTTCCAGCACACA[A/G]TAGCAAGTAAATTCA	78514
rs211874872	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77258474	CTGACTTGCTTCTCT[A/G]TCTTCAACAAACTGG	78514
rs211883376	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77507146	ATCCAGGTGTGGTCC[C/T]CCATGCCTGTATTCC	78514
rs211885054	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77500950	CAAACTACACAATTT[A/G]AATGAATGGACTGGG	78514
rs211886495	in-del	-/A			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77485407	TGGGAGGAAGGCAAG[-/A]ATGCCTGTCCTGTGG	78514
rs211887894	in-del	-/TG			intron-variant	Arhgap10	Mm_Celera	8:77446968	TGGGGTGCCTGTGGC[-/TG]TCTCTCACTGCTTCT	78514
rs211904933	snp	G/T			intron-variant, synonymous-codon	Arhgap10	Mm_Celera	8:77476630	CTCTCAACACAGGCC[G/T]AACCAAGTATCTGCT	78514
rs211908379	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77352249	GCTGAGGGTCACCAC[A/C]ACATGAGGAACTGTA	78514
rs211913328	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77381854	AACCAGCAATAAGGC[A/G]CTTGAACAAAATGTG	78514
rs211921370	in-del	-/TGAACATGCTGCTGACAGC			intron-variant	Arhgap10	Mm_Celera	8:77445089	TCTGGAGTAGGCATA[-/TGAACATGCTGCTGACAGC]TTAAACAGATAGGGA	78514
rs211923198	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77298569	GAGAGATGGCTCAGC[A/T]GTTTAGAGCACTGAC	78514
rs211954076	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77337343	AATCCTGTCTTGGGC[A/G]GTGCTGAAGAGAAAC	78514
rs211961708	in-del	-/ACCACATG			intron-variant	Arhgap10	Mm_Celera	8:77310087	TATACTCTACACAAA[-/ACCACATG]ACCACGAATCACCAA	78514
rs211973188	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77375805	ACAGTGAGAGGAAGA[C/T]GAAAACATGAGCGTG	78514
rs211977907	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77430161	GTGTTTAAATGTTTG[A/C]GTCTACTGGGTACCA	78514
rs211985263	in-del	-/AAAAAA			intron-variant	Arhgap10	Mm_Celera	8:77418937	AACCCCTGGTCTAAG[-/AAAAAA]AAAAAAAAAAAAGGT	78514
rs211985302	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77370638	CCAGCATTGTTTCTG[C/T]TAGCTGTGGCTTTGC	78514
rs211986394	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77283991	GGAACCCAGAACATT[G/T]GGGTGGGTTGCAATG	78514
rs211990672	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77447839	GCGAGCAGCCAGACC[A/G]GTACTGGAGCTGAGA	78514
rs211997251	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77331815	GCCAAGACAGCCTGG[C/T]GACATAGACCGGGTG	78514
rs212004537	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77441426	CTTCCAACAAACCCC[A/G]CCACCAGAATAAGAC	78514
rs212006323	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77275584	ATCTATTTAATGCAC[A/G]GCATAAGAAGAAAAG	78514
rs212009973	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77325456	ATTCACACATGGCTG[C/T]TTGCTTCTGCTGCCC	78514
rs212012137	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77489554	GCTAAAAAGGCATTA[G/T]GCGAGTTTACCCACC	78514
rs212030670	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77375405	CAATGCAATAGCCAC[A/C]GTGTTCTTCCGAGCA	78514
rs212032523	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77482082	GCCACTGCCACAATA[G/T]TCTCTCAGGAAGAGC	78514
rs212034274	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77461468	TCAAAACAAAAAGTC[-/AA]AAAAAACCACCAAAA	78514
rs212048223	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77371147	TATTTAATAGAAATG[A/G]CTCATGGAAAATGTG	78514
rs212051307	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77453249	TAACATGTAAGAATG[C/T]TCCTGTCTCCTTTCC	78514
rs212066249	in-del	-/AG			intron-variant	Arhgap10	GRCm38.p3	8:77447376	TCACAGCCAGCTAAC[-/AG]AGTCTCTAGGAACCG	78514
rs212076591	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77325934	GACCAAGTTCTGCCT[A/C]CTCCACCCTCTAGAT	78514
rs212076831	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77357344	CGCCATGCTCCCCTT[C/T]CGGGGTCTCACTGTA	78514
rs212083531	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77274025	AGAAGGTGCAGTCCG[-/T]AAAGACAAGGTAAAG	78514
rs212092556	in-del	-/CTGCTGTTG			intron-variant	Arhgap10	Mm_Celera	8:77384014	CACCTCAGCACCTCC[-/CTGCTGTTG]CTGCTGCTGCTGCTT	78514
rs212092601	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77313327	CACTCTCTTCACAAG[A/G]CAGGGCCTATCTCCT	78514
rs212103117	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77350122	CATTACCTCCTGATG[G/T]GTAGGAACTTCCTCC	78514
rs212104916	in-del	-/CA			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519950	TCTCTCTCTCTCTCT[-/CA]CACACACACACACAC	78514
rs212108861	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77447065	TGGTTTAAGGGGGGG[A/G]GGGTTTGAGTGGTTG	78514
rs212122148	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77481271	CACACTGTCTACATG[C/T]GAAATGATGGCCCAC	78514
rs212127859	in-del	-/TTT			intron-variant	Arhgap10	Mm_Celera	8:77360868	CTTCTAAAGGAACTC[-/TTT]TTTTTATTTCCAGTT	78514
rs212132107	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77274908	GAACTAACCAGTACC[C/T]CCCAGAGCTCGTGTC	78514
rs212134772	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77386362	GTCTTGAACTCGGAT[A/C]CTAACTCCACCTCCC	78514
rs212134967	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77297549	TATATTTGGCCATGT[A/G]CCTAGCTGAAAACCA	78514
rs212140729	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77399642	GACTGTGAGGTCACA[A/C]TTCCTAACTCACGTT	78514
rs212147483	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77440238	AACTCTTCAAAATGA[A/G]CATTTCATCACCAAC	78514
rs212156023	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77252444	CTAAGAGCCCTATTC[C/T]TAAAGGTTCTATCCA	78514
rs212168993	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77428951	AGGTTTTTTTTTTTT[-/A]AATTAGATTTTCTTT	78514
rs212184604	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77289901	CTCCTCAAAACAAAC[A/G]GAATCAGAGGAAAGT	78514
rs212189290	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77270413	ACCCCAAATCAACTC[A/C]CCCCTCACAAGGCTC	78514
rs212192246	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77461469	TCAAAACAAAAAGTC[-/A]AAAAACCACCAAAAC	78514
rs212202180	in-del	-/GCTCTGCTAT			intron-variant	Arhgap10	Mm_Celera	8:77416288	GGATACAAACCCTCA[-/GCTCTGCTAT]GCTCTGCTATGCTCC	78514
rs212206636	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77387760	AGTTCCCTGGGCTTT[C/T]GACAATGCCCCTGCG	78514
rs212228949	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77343167	CGCTACAAGTGCAGC[A/C]GGCCGGGTAAGAGTT	78514
rs212242301	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77427608	TTCTCGTTGACTGCT[A/T]TCAGAGCACAAAGTC	78514
rs212244430	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77447544	TCTGTGGGGAAGACC[C/T]GCCAACAGTGCTCTG	78514
rs212258561	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77362578	ATTCCTCAGAAGACA[C/T]TGGTTGGCTTGAAAA	78514
rs212265745	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77274019	AGGCAGAGAAGGTGC[A/C]GTCCGTAAAGACAAG	78514
rs212278897	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77290617	GGTTTTTAACTTCCC[G/T]AATGCTATGACCCTT	78514
rs212293104	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77448829	CACTGCCGCATCCCT[A/G]GCCCTGTGCACACTG	78514
rs212311920	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77420991	AGATTAAGGAAAACA[C/T]TTCTTCCTGGAACAG	78514
rs212331584	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77463725	ACTCCTTGGGCCTAT[C/T]AGAATGCCAACAAGC	78514
rs212335342	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77268959	AGCCGCATGGCTTAC[C/T]ACGGCAATGGTCTCT	78514
rs212340335	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77318485	TTTAAAATAACCTAA[A/C]AGCCTGCCTTTCCAA	78514
rs212364938	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77506699	GATACATCCGGTTTC[C/T]TCAAGTGTGACTGTT	78514
rs212371184	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77263344	GAAGGGAGACAGGGT[A/G]AGAGAAAGTACTGAC	78514
rs212371453	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77269486	TGCTCCTCCACACTT[A/G]TCTCTCTGAATCCAC	78514
rs212373092	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77370168	TGAATTAATAGAGCA[C/G]GGTACAGATAAAAGC	78514
rs212398944	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77319178	GGGGAGTAGCGGGGA[A/G]GGTATGGGAGTCTTT	78514
rs212401235	in-del	-/A			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484116	CCTAACTCCTCCTAC[-/A]AAGCTTACTGAAGAA	78514
rs212401956	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77300174	AGGAGGAAAAAGAAG[-/A]AAGAAGGAAGAAGAA	78514
rs212418918	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77433990	CTTAGTTGCAAAAGA[A/G]CCCTGGCAACACACA	78514
rs212420049	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77446789	TGAGGTATTTGTACT[C/T]GAAATGTATATATTT	78514
rs212420283	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77460404	AAAGTAGCAATATTA[A/G]CAAGAAAGAAACATT	78514
rs212422028	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77404922	AGGCGTGTGCCACCA[A/C]GCCTGGCTGCAGAAA	78514
rs212434362	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77368068	GGCACATTAGACATC[C/G]GGTCTTATAGGATTT	78514
rs212439282	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77433014	AGGGAAAGGAGCTGG[A/G]GCAGCTGGGGGGAGC	78514
rs212455220	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77280447	TAACATCCCTCTCCC[C/T]GTCCTGTCCAGGAAT	78514
rs212457537	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77263744	AAGACTCCTGTTTCT[C/T]GAGGACCCGGAGTCC	78514
rs212482487	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77398995	ACGTACTGGGTTAGA[A/T]CAGTCACATTCTGGG	78514
rs212485160	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77381316	ACCTAGGACGGTCAG[C/T]CCAGGAGTGGCACCA	78514
rs212489090	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77440640	ATATGAAATAAAAAA[C/T]ACACAAGTTTTTCAT	78514
rs212499493	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77451600	AGGGCTCTGCCACGA[C/T]CACTTCCGAAGGGAA	78514
rs212510702	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77424741	CAGAAAGCAGTTTTA[C/T]GCTTTTGTTGGGAAG	78514
rs212528371	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77336877	AAAACCACCTGACCT[A/C]TTGTTTTTCTCAAAA	78514
rs212560674	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77447542	ACTCTGTGGGGAAGA[-/C]CCGCCAACAGTGCTC	78514
rs212564484	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77512284	AGATTCTCTTTCAGA[A/G]CCAAAGACCACCAGC	78514
rs212575279	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77316629	CATGGCCATTAAAAC[-/T]CTGACAATATTATGA	78514
rs212575720	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77430996	TTCAAACTAAGAGAC[C/T]AAAGTCTTTGTAAAG	78514
rs212589294	in-del	-/CACA			intron-variant	Arhgap10	Mm_Celera	8:77487343	ACAGGCGCATGCACG[-/CACA]CACGCACACACAGAT	78514
rs212591921	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77409099	GAAAACTAAATGTTT[A/C]GAAGTTATTTTGTAA	78514
rs212596843	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77416120	TCTGGATAAGGCTAA[A/G]ggggggggggggggg	78514
rs212603381	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77511719	ATTTCTGAGTTCGAG[G/T]CCAGCCTGGTCTACA	78514
rs212604268	in-del	-/ACACAAACACACACAA			intron-variant	Arhgap10	GRCm38.p3	8:77414906	CACACACACACACAC[-/ACACAAACACACACAA]ACACACACACACACA	78514
rs212606848	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77427061	AACCCTAAGACCTTC[C/G]AGGGAAGTCATCGGA	78514
rs212610018	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77473473	AGCAGACTGTGCAGC[A/G]GAGTCCACTCGGCAA	78514
rs212613367	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77457857	CTTTTGTTTAAAAAG[A/T]TCTAGTAAAAACAGC	78514
rs212614354	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77467789	AGACTGACCCTTCGG[A/G]CAAAGGAATGCGATT	78514
rs212619017	in-del	-/AAATAGGC			intron-variant	Arhgap10	Mm_Celera	8:77290478	TTGGAAACCAAAGGG[-/AAATAGGC]CCTGAGTGAAGCCTC	78514
rs212623648	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77363064	TTCCCTGCCAACAAC[A/G]GAATGACGTCCTAAC	78514
rs212635755	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77330682	GCAAAGAGGGAAACG[A/C]CAGGTAAGTAAGTTC	78514
rs212642799	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77439188	CTAAGGACTGAGGTC[A/T]ACGGTGTGTAGGTCT	78514
rs212652167	in-del	-/AGAC			intron-variant	Arhgap10	Mm_Celera	8:77334986	AAGACAAGACCTGAA[-/AGAC]AGACAGCGCGCCCAG	78514
rs212652748	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77469848	ATTCCACCAGGCGTA[G/T]GCTCTTAAGTGCCCT	78514
rs212658708	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77480088	CCAGAAAGAGAAGCA[A/G]CAGCTCTTTCCACCC	78514
rs212667062	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77369318	CTAAACCCCCAGATG[C/T]GTGGCATCTTAAGTC	78514
rs212669732	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77404664	TGCAAAATAGCAAAA[A/G]CAGATACTTGGAAAG	78514
rs212669932	in-del	-/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503488	GACACCCACCCTTCA[-/G]GTAAGTCACATGTAA	78514
rs212676157	in-del	-/ATT			intron-variant	Arhgap10	Mm_Celera	8:77459198	TTCGTTAAAGTTCTC[-/ATT]TGACTCTCTCACATG	78514
rs212707419	in-del	-/ACAC			intron-variant	Arhgap10	Mm_Celera	8:77457889	GAGCGCACATGCATG[-/ACAC]ATACACACAAAGATA	78514
rs212709299	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77438581	TCTGCCATTGAGAAA[G/T]CATTCCATCTTCACC	78514
rs212717994	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77356863	AAATAAGTTGATTAA[A/G]TATGACTTGATCTGA	78514
rs212721383	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77464984	TACGTAAGATTACAA[C/G]AATACAGGAAAATAA	78514
rs212729759	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77312546	GCAAGGTGCAGGTGC[C/T]AGCCATCCTTGTGCC	78514
rs212735307	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77397985	CACTGTCTTCCATGC[C/G]GCAAAGGACAGTCAC	78514
rs212736080	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77475496	TTCCCAGCACTCATA[C/T]GATTCACAATTCCAG	78514
rs212756727	snp	C/T			synonymous-codon	Arhgap10	Mm_Celera	8:77384785	AATGGCTCTGTTAAA[C/T]GTGTGGAACAGCTAG	78514
rs212757351	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77457560	GGCCAAGAGGTGAGA[A/G]TGGGTGTGAGAGGGT	78514
rs212769367	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77413346	CGGAGCTCCATGCTA[C/G]TGCAGAAGCAGGAAT	78514
rs212769489	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77419830	ACAACTCAGAGCTAA[C/T]ATAACCAAGTTTACC	78514
rs212773236	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77256417	CTCCGCAAAGCCCAA[C/T]CTTGTGTGAGGGTTG	78514
rs212774888	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77295430	GTAGGAAAATGAACA[A/G]TATGTAGTCCTATAT	78514
rs212795247	in-del	-/AAGAG			intron-variant	Arhgap10	Mm_Celera	8:77475898	TTTAATCTTAAGTAT[-/AAGAG]AAGACACTGGCCAGT	78514
rs212822217	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77274821	AGGTGGTTCTGAAGT[A/G]TGCTCACTGAGCTAG	78514
rs212824393	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77415556	CACGCTGCCTGGGGG[-/C]CCCCGCTTCCTCGTG	78514
rs212825692	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77462960	CCAGGGTGGCCCAGT[A/G]GACGTTAGAAGCACA	78514
rs212829107	in-del	-/AGT			intron-variant	Arhgap10	Mm_Celera	8:77258158	TAAGGGAAGCAAGGC[-/AGT]AGTAAGCAGCATTCC	78514
rs212831524	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77468220	GTGTGCTCTCACTTG[G/T]GTGGTTATGGGGAAG	78514
rs212834403	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77419194	GGGGCAGAGATCACA[A/G]GATGGTGGGACGGGT	78514
rs212847891	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77251500	GCTTCAACCCATCAA[C/G]CACTACCGGAATCAG	78514
rs212849505	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77348999	TAGGCTACAGAGAAT[A/G]AACTACCTCGTAAGC	78514
rs212851056	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77340744	ACACCCTGTCCACAC[C/T]CAGCCAGACTCCCTT	78514
rs212852546	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77486614	AGTGCACTAGAAAAA[-/T]GCAAGCACCGTATTC	78514
rs212859472	in-del	-/A			intron-variant	Arhgap10	GRCm38.p3	8:77308028	AACAAACAAACAAAC[-/A]AAAAAAAAAACTATA	78514
rs212864692	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77335709	TTGGGCAGTGAAATA[G/T]AAGAATCAAAGTACT	78514
rs212867852	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77296065	GTGGGTGTGGCTTTA[A/C]GACCCTCATCCTAGC	78514
rs212870930	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77431485	ACCTGCTGCCAGAAA[C/T]AGGACTTAGGGATAG	78514
rs212888001	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77462653	ATAGCTTTCACTGTG[A/G]AGGTCTTTGCTCTGT	78514
rs212890219	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77505552	CAGAGACAGGTGAAT[C/G]TCTGTGAGTTTGAGG	78514
rs212896854	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77455370	CACAGGCCAATACAA[C/T]GGAGGCAATGCCTTA	78514
rs212905386	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77491795	GACCAGGGAGTCAAC[A/G]TGGCCTCTGGTGGTA	78514
rs212906309	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77407769	ACAGACCTTAGGAAC[C/T]GAGGTGGGCACAGGA	78514
rs212911925	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77341557	TTCAATCACAGCCAC[A/G]CCTCCTGTCCAGTGC	78514
rs212916203	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77281097	TCCTGTGAATAGAAA[C/G]AACAAAAATGATACT	78514
rs212926854	in-del	-/T			intron-variant	Arhgap10	GRCm38.p3	8:77387166	TTTAAAACTCTTCTA[-/T]TTTTTTTTTAGTTTT	78514
rs212930600	in-del	-/CTCT			intron-variant	Arhgap10	Mm_Celera	8:77325941	TCTGCCTCCTCCACC[-/CTCT]CTCTAGATCCTTTCC	78514
rs212931387	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77291325	GAGAGAGCTGGCCAC[-/G]CCTACAGAGATACCC	78514
rs212939457	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77361396	ATTTTCTTTCCTTTG[A/G]AGAGTTGAAGAAGCA	78514
rs212949210	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77330036	CTGCTGTCCGCTCTC[C/T]GTCTGTGTTGGCTGT	78514
rs212961643	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77317120	TTCACTTTTTCTCGG[A/G]ACCGGAAGCATCCTA	78514
rs212967378	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77273682	GAGGGGATGAGCACA[C/T]GAATAATCTAAACTG	78514
rs212969737	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77383327	TCATACTTTGAACTG[-/A]AAACAGATGATTCAT	78514
rs212975165	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77368508	TCCTCCCACCCCCAT[C/T]TACCCTACACATCCA	78514
rs212989075	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77504368	AGCAAAAGCCAGCCG[C/T]GTGTTGTCAGTGGCC	78514
rs212991320	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77417923	GTCCTGAAAATGAGG[G/T]CAAAAGAACAACTTC	78514
rs213007501	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77460896	TATCCATAAAAAGAT[A/G]TATAACACAGGATTC	78514
rs213013555	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77402924	CAACACAAGCACTCT[C/T]GCTACTGTGCAAACC	78514
rs213014180	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77310097	ACAAAACCACATGAC[C/T]ACGAATCACCAATCG	78514
rs213023322	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77323460	ACAGGAATTTAATCT[C/T]TCTTTCGTACACCTG	78514
rs213040860	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494286	AAGGCTGGGTGCGGT[A/G]GTGTAGGTGGTGTAT	78514
rs213043832	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77355411	GAGGAGGGGAGGGGA[A/G]GAACCATCAATCAGA	78514
rs213046473	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77267872	CTAAGGGCAAGATCC[A/G]GGGCTGCTCCATGGC	78514
rs213056921	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77424011	AGGGCTTTCAAAGAG[A/G]AATGAGAAGGGGCCA	78514
rs213074197	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77467275	CATACGAATAGTCTA[C/T]ATATTCTACTATATC	78514
rs213074532	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77460543	GGTCACCTCAGCCTA[C/T]AAGCATGACACAGAC	78514
rs213077937	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77403309	ACAGCACTAAGGTAA[A/G]CATCCCTACAAGTTC	78514
rs213085721	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77262602	GGCAGGTATAAAGCT[A/G]GAGCAGAAGCTAAGC	78514
rs213096523	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77310964	CAGAGTCCAGCCACA[G/T]TAGACTTGGGGTTCA	78514
rs213098953	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77510603	AGTTTAAATATCTAT[A/C]CAAGACCACAGCTGC	78514
rs213119309	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77333858	GGTGAAAGGATGTCA[A/G]GTGTAGAAATGGACT	78514
rs213125415	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77500307	CATGGTGTGAACCTC[A/G]AGACTTAAAAGTCAG	78514
rs213127133	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77286528	GCATGCATGGTACTG[A/G]AGCAGTAGCTGGAAG	78514
rs213149163	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77278740	GAAGCATAAGACAAA[C/T]CGTGGGCCCTGAGTA	78514
rs213153735	in-del	-/AAC			intron-variant	Arhgap10	Mm_Celera	8:77370598	GCTTTTTTGGGTGAG[-/AAC]AACTGTCTTGTGTAC	78514
rs213165381	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77251191	TCTAGTACCTGTTTC[C/T]AATCTTGCCCCTTCT	78514
rs213199082	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77272536	GGCATATCCTGCCCC[C/T]AACCCTGAACTTTCC	78514
rs213211827	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77287366	CATAATGCCAGCCTG[C/T]GTTTCCTATGGTTCC	78514
rs213224443	in-del	-/TATA			intron-variant	Arhgap10	Mm_Celera	8:77407428	AGATAGATAGATAGA[-/TATA]GATGGATGGATAGAT	78514
rs213227561	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77444258	GGCTTTTTAGAGATG[C/T]TCATAAATGCTGCCA	78514
rs213230588	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77328231	CCAGATTTTGAAGAC[A/G]AGTTAGTTACCACTG	78514
rs213270030	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77412164	ACATCCCGAAGAGTC[G/T]GAGGCTGAACCACGA	78514
rs213289472	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77328636	TACCAGAGCACATCT[A/G]CACCGCCCATACCGC	78514
rs213312290	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77499219	GCATGAAGGGAAGGG[A/G]GGGCATGTAATGAAT	78514
rs213323798	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484195	AGACCAAACTAAAAG[C/T]CAATGCTCTAGCCGC	78514
rs213325168	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77272820	CTGCAAATCTGGTAT[A/G]TAGAAATGGAGGTAA	78514
rs213339664	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77396183	CACCACGGAGGGCTA[C/T]ACGGTGCATCATTTC	78514
rs213345735	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77448698	ACACTGCCGCATCCC[C/T]AGCCCTGTGCACACT	78514
rs213346474	snp	A/C/T			intron-variant	Arhgap10	GRCm38.p3	8:77307353	ATAAAAGCAACTTTA[A/C/T]GAAAGCTCAAAGCAC	78514
rs213362906	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77345763	TTGTCTGCTCCCTAG[C/T]TGAAATCGTTTTAAC	78514
rs213363208	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77354049	TACAGTGCTGCTTTC[A/G]TGGGAGAATAAAGAC	78514
rs213381338	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77483777	TCTGCTGTGCCTCAA[A/G]CCTCTCCCTACTGCC	78514
rs213381409	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77491273	CTCATATACATAAAA[C/T]AAATAAATCTTAAAA	78514
rs213381672	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77293146	AGGCCCCCATGCTCA[C/G]GAAGTTGGTACCCAG	78514
rs213396825	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77396470	GCAACGCTCTATTAA[C/T]GACAAAAGTCTTGAG	78514
rs213420858	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77408194	ATCACGGCCGACTAA[A/G]AGCATACAGCATCAT	78514
rs213439901	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77474810	AAAGGTCACTGACTG[-/A]AGGTCATGGGTCGCA	78514
rs213461001	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77361961	GGCTTCGCCCTAGAA[A/G]GAGAGCGGTCACTCA	78514
rs213461978	in-del	-/GATT			intron-variant	Arhgap10	Mm_Celera	8:77410670	AACTGAATGAAAGGG[-/GATT]GATTCACTCAAAGGT	78514
rs213463070	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77428538	ACCCCATTTTTAAAT[-/G]CATCACTTAACCAGT	78514
rs213463227	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77293777	TATAATAATAATGCC[C/T]AAAAAGTAGGAGGGC	78514
rs213467266	in-del	-/TATTAATCC			intron-variant, cds-indel	Arhgap10	GRCm38.p3	8:77492051	AGGGCTCTTCTGTGA[-/TATTAATCC]CCAGATTCACTCTTT	78514
rs213472654	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77296186	TTCCCACCTTGGTGA[-/T]TAATGGGCTGAACCT	78514
rs213478677	snp	C/T			downstream-variant-500B	Arhgap10	Mm_Celera	8:77249865	CAGTGATACAGAACT[C/T]CCTTCATAGTCCAAA	78514
rs213487569	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77317498	AAACCTCTTCCAAGT[A/G]CACATGCAAGGTCTC	78514
rs213489573	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77423320	AATACTGGCCCTGGC[C/T]GCCCCAGGGACGAGG	78514
rs213505853	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77382413	CTCCTGTGCTCAGCC[-/A]CCCCACCTCCTGAAC	78514
rs213507415	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77271506	GTATGGGGGCTCTGT[A/G]ATATATGGGAGGTTT	78514
rs213507567	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77383624	TAACATTATATAAAA[C/T]GCAAGTTGTTTCCTC	78514
rs213517157	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77423924	CCTGAGCAGGTGTGC[-/A]AGTGCATGACACATG	78514
rs213518321	in-del	-/ATGGACTGGCC			intron-variant	Arhgap10	Mm_Celera	8:77456292	AATTCTTCTAGGACT[-/ATGGACTGGCC]TCAAACATTCTTTCA	78514
rs213518964	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77454130	ACCTGGAGAAGCGCA[C/T]GGGCTGGGACCCCTA	78514
rs213521997	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77466356	AGATACAGAAGAATC[C/T]TGATGGGAAATACAG	78514
rs213527251	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77327294	ACCGATAACTGTTAG[C/T]TCTGCTCTTCCCGAG	78514
rs213529490	in-del	-/CACACACACACACACACACA			intron-variant	Arhgap10	GRCm38.p3	8:77433417	CCCTTCTCTTGGCCT[-/CACACACACACACACACACA]CACACACACACACAC	78514
rs213538561	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77265678	GTTAGGGTGGCCATG[A/G]CTGGTGCCATGGAGC	78514
rs213539017	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77271886	CGAGGAGCCTGGGCT[A/T]GCAACTCTTCACTGG	78514
rs213542162	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77339367	GGATTATAGTCCTAA[C/T]CATCTAAAATGATTA	78514
rs213559568	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77435623	TGTGTCAAGTTGACA[-/C]AGAAACCCATCCGGT	78514
rs213565406	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77488618	TGTGCCCAATACATG[-/C]AAAGTGCTAGGCTAT	78514
rs213566482	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77384063	TGCGTCCTGAAGAGC[A/G]AGCGCATGCTTTAGC	78514
rs213575634	snp	A/G			intron-variant, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77517614	GCAGCCCGAACGCGA[A/G]CAGGACCCCGCTTAC	78514
rs213597174	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77339986	AACAACACAAAACAA[A/G]GCATCCGGCATCAAA	78514
rs213614285	in-del	-/AAAAAA			intron-variant	Arhgap10	Mm_Celera	8:77341726	TCTGAAATGTCTATC[-/AAAAAA]AAAAAAAAAAAAAAA	78514
rs213615133	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77265935	AAGCCCAGAGAGGTG[A/G]CAGGGATTTGCTCAA	78514
rs213620218	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77410878	AAGACTGAGGAGTGT[A/G]ATTTAGAAACAAAAC	78514
rs213625521	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77296626	CTCAAATATTGGCAG[-/A]GGAAAAAAAATCTAC	78514
rs213635756	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77429443	AGCCAGTGAGCATGC[A/G]CTCACAGCACAAGTG	78514
rs213647111	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77366210	GTGGAACAAGACTAA[C/T]GCAGGGTCCAAAGGT	78514
rs213652607	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77370783	TAATCAGCCTCACTT[-/C]CCCCTCAGAGGACCA	78514
rs213662944	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77443375	AGAGTATATGATCAG[C/T]CATGGAGGAACACAG	78514
rs213670833	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77334371	AGTCCAGGAATACAG[G/T]GGAGTCCATGGAGAG	78514
rs213672136	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77472394	TTGAGAGATGGCTCA[A/G]TGGTTAAGAGGTTAA	78514
rs213687536	in-del	-/CCTC			intron-variant	Arhgap10	Mm_Celera	8:77479111	CCCCAAGCTCTGGCT[-/CCTC]CCTCCCTCCCTCCCT	78514
rs213688117	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77279266	CAGCTTCAATTCTTT[C/T]TCGAATGGAGTTCCC	78514
rs213701880	snp	G/T			intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77492690	GGAAAATGCCTGCAT[G/T]TTCTTTAAGATATTT	78514
rs213703055	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77470929	GAACTGAGCCCAGGT[C/T]CTCTGGAAAAGCAGC	78514
rs213704056	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77412649	CATGGGATACTCGTG[A/G]GGACACCTCAACTTT	78514
rs213705232	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77436639	GCTGCTAGCAAAGCC[A/G]GGCTGAATATAGAAG	78514
rs213717241	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77368249	CTGCACCAGCCTTTT[-/C]TTCCAAAATTCTTTC	78514
rs213728699	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77359975	TAACACATCAAGGCA[C/T]GGGAAGAATTACATG	78514
rs213739068	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77455702	ATGGAAGAACACCCA[G/T]CCTATTGTGGGTAGT	78514
rs213740383	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77515584	AACCCTTTTATTCTT[A/G]AGGGGAAGAGTGTAA	78514
rs213747863	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77315826	ATTTATACTATATTA[A/G]TGGTAAGAGAACTTA	78514
rs213759408	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77376360	TATTAGTTTAGTTCA[A/G]TCCTTTATTTAAAGC	78514
rs213765572	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77470682	ATTTAGTTTCGAATG[A/G]TAGTGTAAGTTCATC	78514
rs213766110	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77259773	ACCCATAAAGAGATC[C/T]GACATCCTCTTCTGT	78514
rs213774781	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77447029	CTTTTGAGGGGTAGG[-/A]TTTTTTGTTTTGGTT	78514
rs213777675	in-del	-/ATGCTGTT			intron-variant	Arhgap10	Mm_Celera	8:77464327	GGAGAGCCCTGAGCG[-/ATGCTGTT]ATGCTGTTACAGGAG	78514
rs213778756	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77514539	GTATATGCATGCAAA[C/T]CCAGGTGCCACAGAG	78514
rs213790165	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77477553	AAAAGGGCCGAGTTC[C/T]GTCATCTAACTATGT	78514
rs213791134	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77441897	GAGACACTGGTTGCT[A/G]GAGCTGCATTGTTCA	78514
rs213814392	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77290073	TGTAATATTTTGATT[-/A]AAAAACTTCAAAAAC	78514
rs213816457	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77371698	CCCAGGTCTGCTCTA[C/T]ACCCCTTACGCATGT	78514
rs213832658	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77382321	AAGGACATGTATGTA[C/T]ACACACAGGAAAGGC	78514
rs213844140	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77441332	CTCCCTCTCCCTGCA[G/T]CAGGGACAGGACTAG	78514
rs213844526	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77326540	CTGGTGTAGGCTCAC[A/G]CTCATATGACTCGTC	78514
rs213846141	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77457425	GAACTAACCAGTACC[C/T]CCCCAGAGCTCGTGT	78514
rs213855524	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77308931	TACTGTTAACAGACA[C/T]TACTCAGCCATTAAT	78514
rs213870371	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77338191	CTGCTGGGAAACTGT[C/T]ATCTGCAGTATGCAA	78514
rs213874349	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77254133	AGATCCACCAACAGA[A/C]TGTATTTCTGGGATT	78514
rs213878466	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77416722	TCTATACATATGGAG[A/G]ATGAGGAGGAAAAGA	78514
rs213879332	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77435432	CAAAGCTACCTAAGA[A/G]CACTCCTACGGTCTG	78514
rs213885586	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77364841	TGGAAACCATGCAGA[A/G]CACAGAGGCCTGACT	78514
rs213905783	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77322995	AGACACGTGCCAGCC[-/A]AATCTGAGGAGAAGG	78514
rs213908521	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77400302	ACCCTAGGAGACACC[G/T]TCTAGTTTCACTTAT	78514
rs213913267	snp	C/T			intron-variant, missense	Arhgap10	Mm_Celera	8:77476596	AGTACTAGGCAGCAA[C/T]TGTGGGCTCCATAGC	78514
rs213916181	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77387704	TCATTTTCGGCAGCC[-/A]ATCACCTCACGACTG	78514
rs213918970	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77284959	AACATCTAGGTCCTG[A/G]GAGAGGAAACAAACT	78514
rs213923943	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77352143	GACCAGTGGTCCCCA[A/G]CCCCTTTGGGGCTGG	78514
rs213940418	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77332260	CGGGGTGGCCCACCG[C/T]GTTCATGCTGCTTGC	78514
rs213947775	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77298385	ATGAACAAAAATTAT[C/T]TCAAATAAATAAATA	78514
rs213958899	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77465176	GCAATGGATCTGAAG[C/G]CCCGCAAACCTTGAG	78514
rs213964095	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77400779	GTGTGTTTTCCCTCT[C/T]TGTACACATCTCTAT	78514
rs213965176	in-del	-/AGG			intron-variant	Arhgap10	Mm_Celera	8:77376937	GCCCAAGCCAATGTC[-/AGG]AGAATTCTCCAAAAA	78514
rs213966095	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77423126	GGTTCTCGCTCTGAC[-/G]AGCACTATTCTAGGC	78514
rs213988646	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77253037	TGCTTCCATCTTTGG[A/G]CTATTTTTGAGTACT	78514
rs213993067	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77276156	ACATGCACATTCTTG[A/C]ACACACCAATGCATA	78514
rs213993593	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77508772	CAAGGTAGTAAGGAG[A/G]CTAAAGCAAGGAGAA	78514
rs214000587	in-del	-/CTAA			intron-variant	Arhgap10	Mm_Celera	8:77477559	GCCGAGTTCCGTCAT[-/CTAA]CTATGTGGCCCTATG	78514
rs214005789	in-del	-/ACA			intron-variant	Arhgap10	Mm_Celera	8:77432908	AAAATGAACAACAAC[-/ACA]ACACTTGGCTGTTTT	78514
rs214006373	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77365574	TTTTAAAAAAGAGAG[C/T]TGCCATAAACTCCAT	78514
rs214012046	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77464767	TTACCTAGGGCTGGA[A/G]AGCTGGCTCAGCGGT	78514
rs214016153	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77291410	GATACCCAGCACAGG[A/C]AGCATGAAATGCAAA	78514
rs214016164	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77305559	CTGTGCCACACGTGC[A/G]AACACATCTAAGACC	78514
rs214017283	snp	A/G			synonymous-codon	Arhgap10	Mm_Celera	8:77277297	CTCCTTGAGAGGGCT[A/G]GGACTGTCACCTAGA	78514
rs214028024	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77345020	CCCTGCTCTCCAGTC[C/T]TCCTTCTCCTTCTGT	78514
rs214028451	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77472784	GATCCAGAACCCAAG[A/G]AAAGCTGGGCACTGT	78514
rs214042463	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77320929	AGTCAACCCAGACTG[C/T]CAACGTGACAAGCTC	78514
rs214047634	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77495421	GCCACCCCAAGCTGA[G/T]GACCCAACCAAGAAT	78514
rs214067394	snp	C/T			upstream-variant-2KB, downstream-variant-500B	Arhgap10, 0610038B21Rik	Mm_Celera	8:77518589	GTAGGAGAGGCGATC[C/T]GCTAAAAATAGCCCG	78514
rs214075881	in-del	-/G			intron-variant	Arhgap10	GRCm38.p3	8:77449599	AGAAAACATGGCTGT[-/G]TTACTTTGAAAATCA	78514
rs214084847	snp	C/G			intron-variant, downstream-variant-500B	Arhgap10	Mm_Celera	8:77358180	CTCCACTACGCCCTA[C/G]TCCCCCCATCTCCCT	78514
rs214093776	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77497302	GTGGGTCCTCTGCTA[C/G]AGCAGCCGGTGCCTT	78514
rs214097872	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77270372	TACAGAGAACAGGAG[A/C]CGGTGGAAGGCTCAG	78514
rs214103581	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77265054	TGAGCACTGCTGGCA[A/G]CGGAAGGCCAGTTCC	78514
rs214110502	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77439486	TCGAACTACAGTTCT[-/A]AAAACCTGTTTTAGA	78514
rs214113953	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77371100	CCCACATTTATAAAA[C/T]AACAGCACATGCTAG	78514
rs214118021	in-del	-/A			intron-variant	Arhgap10	GRCm38.p3	8:77404516	ACTCCTTCCAAAAGC[-/A]AATAAATCTAACCAA	78514
rs214118264	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77314251	TTATATCCTTTTTGC[A/G]TCTCAAGGAGGAGAT	78514
rs214133895	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77460131	ACAGCCAGGGCTACA[C/T]AGAGAAACCCTGTCT	78514
rs214136998	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77325833	AGAATCACCATATAT[A/T]CACATATTCACAATT	78514
rs214141496	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77463677	AGAGTTGGAGGGCAC[A/G]GAATGCGAGATTAGC	78514
rs214149094	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77257929	CCCTCCCGAGAGAGG[C/G]GCAACAATAGGGAAT	78514
rs214150400	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77404955	TATTCTCACTGGTTT[C/T]TGTAAGCAGAGAGCG	78514
rs214161739	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77270909	TCAAACTACGTTTCA[A/G]TGGTGTGCTGGAGAG	78514
rs214167383	snp	A/C/G			intron-variant	Arhgap10	GRCm38.p3	8:77420265	ATCCAGAGCACTGCC[A/C/G]TCCGGAGCACCCAAC	78514
rs214169256	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77427055	CCTAACAACCCTAAG[A/G]CCTTCCAGGGAAGTC	78514
rs214182490	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77357411	ATGTGGATTCTCACG[C/T]ACTCATGGGAGCCAA	78514
rs214207292	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77407088	TCTAGTTTCGGGGGA[C/T]CTGACGCCCTCTTCT	78514
rs214208385	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77405169	CCCCAGCTCGTGGGA[G/T]TCATAATCTAACAGA	78514
rs214209288	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77513611	CACAAAGGCCTCAAT[A/C]TATAAAGACTTAGTC	78514
rs214226586	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77436233	TCTTCTCATTAGATG[C/T]AAGGCTATAAGAAGC	78514
rs214227460	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77426462	AGACAATGGTGATTA[A/C]ACATAATCACATAAG	78514
rs214252886	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77284232	ATCCTGTGGCTTCTC[A/G]GGAGTGCAGTATGAA	78514
rs214271826	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77447443	CTCTTCCTCTCATCA[C/G]TTCACTCCAAGGAAT	78514
rs214281252	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77388968	TCTTACCATGTAGCT[A/C]AAGCTGGTCTTGAAT	78514
rs214304207	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77427787	TGCTCCCACCTGGCA[C/T]GAGCTGGCACAAGCT	78514
rs214319860	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77428076	ATGAAGCAGACATAT[A/G]AAATCTAGAGACCCT	78514
rs214320729	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77374946	CTTTTTTCCTCTACC[A/T]GTCTTCAAGAAACTG	78514
rs214342366	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77447123	TTTTGTTTTGTTTTC[A/G]CCCAAGATAGGGTTT	78514
rs214343811	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77501571	AAACTAGACAACACC[C/T]GGTTCCCACTGACTT	78514
rs214344217	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77330772	TGCAGGGAGTAATAT[A/G]GTGGAGATTGTGGCC	78514
rs214344271	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77421638	GTTTAAATGTCAAGT[G/T]AGCAAAATAAGAGCT	78514
rs214350653	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77501231	GTGTCCACTATCACA[-/G]GCTCACTAAACAGGA	78514
rs214356804	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77274098	AGGAGTGCAGAAAGA[C/T]CAGCTGGGCGCTTTT	78514
rs214372821	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77434768	TGGGCCAAGGTATAA[G/T]GTCCCCCCAAAAGAA	78514
rs214407584	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77331344	GGATGCGGTACGACC[G/T]TGGCTAAGTCATGTC	78514
rs214415576	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77476082	AACCTTAGTGAAAAT[C/T]TGGAAACCATCTAAA	78514
rs214418913	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77483592	AAGTCTTGCAGGATC[A/G]GGATCAGGATGTCAA	78514
rs214421187	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77356281	ACAACAGGTAAGAAT[C/T]CTTTGTAACTCCGGT	78514
rs214425575	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77454845	TGCCAAGAAATCCTT[-/A]ACAGCAACCCCCGGC	78514
rs214439112	in-del	-/TAAGACT			intron-variant	Arhgap10	Mm_Celera	8:77268412	GGCTAGACTTTACTG[-/TAAGACT]TACTCATTCTTGGGA	78514
rs214440508	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77332974	GATGTTATAAGCTAA[A/G]ATAATAACATACGCT	78514
rs214452962	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77410461	CACAGCTATTCACTG[A/G]TCACAGCTAGAGGCC	78514
rs214455273	in-del	-/AGCAGC			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77503727	TTTGAGAAAAGCTGG[-/AGCAGC]AGCACAAACGGTGCA	78514
rs214464160	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77451534	CCATGGCAGGTCATG[C/T]ATGGGAAATGAACCA	78514
rs214465118	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77283146	CAAGAGGGAGGGGAG[A/G]GAAGGGGGGGAGGGG	78514
rs214466299	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77446201	CCTCTCGCCAGCCAT[A/T]CTTCAGACCTTTGCC	78514
rs214469420	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77404602	ACCAAATGTTTGCCC[A/G]GGCTCACGAAGCCTC	78514
rs214484910	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77356825	CAACAGGAAGGAAGT[A/G]GCACCACTGTGACGG	78514
rs214498990	in-del	-/CACA			intron-variant	Arhgap10	Mm_Celera	8:77326474	ATGTGTGTGTGTGTG[-/CACA]TGTGTGTGTGTGTGT	78514
rs214502484	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77364692	TCTGGAGAAGAGCCT[A/G]GTGAGAACTGCAAAC	78514
rs214508753	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77296193	CCTTGGTGATAATGG[A/G]CTGAACCTCTGAACC	78514
rs214510618	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77312538	CACAGACAGCAAGGT[A/G]CAGGTGCCAGCCATC	78514
rs214510957	snp	A/C			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494239	GGCTCGTGTGTGAAC[A/C]CACTATTTCTATGAC	78514
rs214513530	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77453674	GGCCAGGTTCCTATC[C/G]TGAAGCACGTGACCC	78514
rs214521189	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77320148	TGGCACACACCTCTG[A/T]TCCCAGCACTTGGGA	78514
rs214526722	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77463056	TGAGTGAACTGTAGA[C/T]GCTTAGACTAGAATA	78514
rs214532682	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77405369	TTTCTAAGATTTTTT[-/A]AAATTATGTGTTTTT	78514
rs214545388	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77349917	ACAAGTCCATGCGGG[C/G]AACTATGGGAAGTAC	78514
rs214548738	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77496928	ATTCTGCCACAGGGC[C/T]GGGCAGTGGTAGCGC	78514
rs214558379	snp	A/C/G			intron-variant	Arhgap10	Mm_Celera	8:77506082	CCACCACCCCCCCCC[A/C/G]CCCCCCCCCCCGCCT	78514
rs214562298	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77433888	AAGTGGACATCCATA[G/T]TACAAAGTGAAGAAT	78514
rs214576275	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493756	CTGCCGAACAGAAGG[A/G]GCTCGGAAGCATCCC	78514
rs214585641	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77459503	GCTTCGCCATTTACA[G/T]ATTTACCTTTTGTGG	78514
rs214596855	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77252061	CACCATGCCTTCTGA[C/T]AACTGTCTTCCACCT	78514
rs214597711	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77387490	CTGCTGAATGAGAAA[C/T]GGGTCTGCCCAGAGA	78514
rs214616425	snp	A/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77502473	GCAAAAACTGTGGCC[A/T]ACTAACCCTAAGCAC	78514
rs214625784	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77273280	ACTCTGCATCCTGGA[A/G]GTGAAGATTAAGCTA	78514
rs214626250	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77343063	ATTAATCCATCAGCA[A/G]TCACTCCCTGTGGAT	78514
rs214643603	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77469479	GACTGTATTAAAGTG[C/T]TGCAGCACTAGGAAG	78514
rs214652277	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77330012	AAACCTATAAGCCGT[A/T]AAGCTTCACTGCTGT	78514
rs214655647	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77381993	GGGGCCTTTAAGGAG[A/G]TGGTTAGGGTATTAG	78514
rs214668362	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77381251	GACCATGGAGGAACA[C/T]AGTTCACTAGATGAA	78514
rs214676369	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77290432	TTCTCATTATGATTA[C/T]AATCCATGCAACAGC	78514
rs214676671	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77253375	GTGTGAAGTGCTCCC[C/T]TCTCCAGCGCTGGAA	78514
rs214686015	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77452816	GTTCTTCCAAGGGAC[A/C]AGGGTTCACTTCCCA	78514
rs214689571	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77337417	TGGTTCCAGAGGCAG[A/C]CGTCTAGCCCATACA	78514
rs214690764	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77513244	TCTTGCCTGGGTCTT[C/T]CCAGCGCAGTTGGAA	78514
rs214693679	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77336777	GTGAGGAGCATCCAG[A/C]ACACTTGAGGTGGGC	78514
rs214709685	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77414643	AAGGCTAGGTGGTGC[A/G]TACCTTTAATCCCAG	78514
rs214715704	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77273623	TCTCAGAGGGGTCAG[A/T]GGAGTCAGTGCAGAC	78514
rs214715790	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77268290	ACTCTGAAGTCACAG[C/T]GCACCAACTCAGAGG	78514
rs214718660	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77282948	CCTTCCTCTCCTTCC[G/T]AATAGTACAGAAACC	78514
rs214726992	in-del	-/A/AAA/AAAA			intron-variant	Arhgap10	Mm_Celera	8:77477218	AAGACATTAGGATTT[-/A/AAA/AAAA]AAAAAAAAAAAAAAG	78514
rs214731987	in-del	-/GGG			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77504273	CACACTGTACAGTCT[-/GGG]GGGGGGGGGGGAGCA	78514
rs214742083	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77408711	CGCGATCTTGGCAAA[C/T]GCTCCCTGTCTACTT	78514
rs214753298	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77268919	ATGGATCAAGGCTGT[C/T]GCCCCACAGGTAGTC	78514
rs214759075	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77409535	TCATATCTAATTAAT[C/T]CCACTCCCTTACCTG	78514
rs214772751	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77458694	ATCTTCTCTTGACTG[C/T]CCAAGGAACAAAGGC	78514
rs214780705	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77500859	ACTATCATTCATACC[A/C]ATCCCGCAAGGCTGG	78514
rs214786133	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77460259	CTAGCAGAGGATCCA[C/T]GGTATACAGCCTCAG	78514
rs214786587	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77363902	AGTCACTTTGACCGA[C/T]TGACTCCAAAATGTG	78514
rs214794926	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77446739	AAAGGCATGCCGTGG[C/G]TTTTGTTAAAGTGGC	78514
rs214802095	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77362997	AATTAATATCTTTGC[A/G]CCAATTCTCTAACTT	78514
rs214805694	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77404159	AGCCCCCTGCTGCTC[A/G]CAGTCCCCTTGGTTC	78514
rs214812656	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77480290	CCACAGCCTACTTCC[A/G]GTCCCCTTTCAAAGC	78514
rs214819102	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77319165	GAATGGGTGGGTAGG[A/G]GAGTAGCGGGGAGGG	78514
rs214821577	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77319688	GCTATAGGGTATCTA[A/G]TGCTAGACCTTGAAA	78514
rs214822220	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77295274	TTCAGTTACCCTAGT[G/T]CTCCTTCTGAGGACA	78514
rs214823837	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77410372	TGGCTTTCTTAAACT[-/G]TGTGGCCAGTTATGC	78514
rs214848567	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77388435	AGTGACAAAGTCAAG[-/AA]AAAAAAAATCAGAAC	78514
rs214851547	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77506549	TAGACACAAAAGCAC[A/G]TCTTAAAATCCTTTT	78514
rs214853242	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77263691	GACAGCAGAGACTGC[A/G]ACTCTCTGGAGCAAA	78514
rs214863183	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77473408	CTAGATGACATGTGT[A/C]CACCATCCATTCCTG	78514
rs214867845	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77264674	ACACACACAGACACA[C/G]ACAGAGAGAGAGAGA	78514
rs214873085	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77430237	GTCTAGGGTGTCCGA[C/T]TGACTCTTACACAGT	78514
rs214877388	snp	A/G			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519835	AATGTCTGTCTCCAA[A/G]CCAACCCACATTGTA	78514
rs214903102	in-del	-/AAAAAA			intron-variant	Arhgap10	Mm_Celera	8:77402689	AAACCTTATTATGAC[-/AAAAAA]AAAAAAAAAAAAGAA	78514
rs214912508	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77257541	TCTGAAGAGAAAATG[A/G]CGGACATGAACATCA	78514
rs214916085	snp	A/G			upstream-variant-2KB, downstream-variant-500B	Arhgap10, 0610038B21Rik	Mm_Celera	8:77519051	CCATTTGAGTGCCAC[A/G]GATGAGGCCACTTTA	78514
rs214924899	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77472927	CTGCGGCAGGGGAAT[A/G]CCTACACTCAGGCGC	78514
rs214926360	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77379428	TCCCCTTACTTAGGG[A/G]GCAGTCCAGCCTCTG	78514
rs214926516	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77335041	GCTCAGGGTCAGGTT[C/T]GGAAGAGGTCTAGGT	78514
rs214940915	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77256266	ACAATTTCAGTGCTA[C/T]AATGTCCCTCCCAAC	78514
rs214945656	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77289785	GGGTGTTCATTCCAA[A/C]CGGCAATGCCATTTC	78514
rs214955821	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77482027	GCAGATTCCGCAGCC[G/T]CAGGGCTTGGTGAAG	78514
rs214969121	in-del	-/TACAAGGTA			intron-variant	Arhgap10	Mm_Celera	8:77339198	GGGGTCTAAAGAGAC[-/TACAAGGTA]TAAAGGTCAGTCCTA	78514
rs214985776	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77380041	AAAAGCACTATGCTA[C/T]CTTCTTCAGAACATT	78514
rs214990433	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77335632	AGCTAGAAAAGAGCA[A/G]ACCAAAACTTGCATA	78514
rs214990437	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77329417	GGGCTAGGTTCGGAG[A/T]AAATCAAGATGGACC	78514
rs214993726	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77336460	TGATAATCCAACCCA[C/G]TAAACAATTGAGCCT	78514
rs215017749	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77280931	TAATTGAGAACTAGG[A/G]GCAGACAACTTATTG	78514
rs215023763	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77361362	GGAGTCAGTGCCCTA[A/G]CCACCACAGACGTGG	78514
rs215037749	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77372084	TATGGCTGCCCTTAC[-/T]TTCCATTCATACAAA	78514
rs215049792	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77282002	ACTGCAGGGATTGCA[A/G]GGAGCAACGTGATCC	78514
rs215050181	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77367720	CCCCCCCTCCCCCCT[A/G]CAGAATTTAAGTAGT	78514
rs215053517	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77475428	TGGGGGAAAACCGGC[A/G]TTTAATATTTACCAC	78514
rs215060538	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77323708	AGCTCCTGCCGTGCA[C/T]GCCCAGACCCCACAT	78514
rs215081215	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77425083	AGCTCCAGAGGATTC[A/G]CCACTCTTCTGGCCT	78514
rs215082187	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77354593	TAAAACTGAACGTGT[A/G]TCTCAGTGTCTTCTA	78514
rs215090709	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77499495	CGGGCTCGGGGCACA[A/G]GGAGATGGGAAGGGA	78514
rs215094702	in-del	-/AT			intron-variant	Arhgap10	Mm_Celera	8:77472633	TATTACTATAGAATC[-/AT]ATACTTTATATAACT	78514
rs215095605	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77309982	AAACAAACAACTCAG[C/G]AAGCATCTTAAATCT	78514
rs215095689	in-del	-/ACACAC			intron-variant	Arhgap10	GRCm38.p3	8:77276171	CACACACCAATGCAT[-/ACACAC]ACACACACACACACA	78514
rs215113038	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77403290	AGGATGGCCCCAGCA[C/T]GAGACAGCACTAAGG	78514
rs215129592	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77378014	GACCTCACCGCTTCC[-/G]GTCACTCAGAGGCAA	78514
rs215138905	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77424691	TGTAGAACATTATGC[C/T]CAGGTTCGTTTGTGT	78514
rs215139357	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77432370	GTAGCAATAGTCTCA[-/T]TCCCAGGTTCCAGGG	78514
rs215139940	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77314482	ACTCTACCTTGTATC[-/T]TTTTTTTTTTTTAAG	78514
rs215141827	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77355249	GGTTCATAGCTATGT[C/T]CTGGTGTTGTGAGTG	78514
rs215146545	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77512217	TAAAGACCCATGGAC[A/G]GCAGCTCACTGAGCA	78514
rs215153126	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77452499	GTTATTCATTTTGCA[A/T]ACGTTCTCAGTCAGA	78514
rs215154679	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77254556	CCCCTGGCACACTAA[A/C]GTACTAAAGGTCCCT	78514
rs215180886	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77294427	GCAGACCACTTTCTC[A/G]TCTTCTCTTTTCTTG	78514
rs215182187	snp	A/G			synonymous-codon	Arhgap10	GRCm38.p3	8:77310744	ACCCTCCTCCAGCTC[A/G]AGACAAAGGTTGTAC	78514
rs215186914	in-del	-/AGAGTTCCCAGAC			intron-variant	Arhgap10	Mm_Celera	8:77289013	GCTCGGCCTTCAGAG[-/AGAGTTCCCAGAC]AGCCAGGGCTATACA	78514
rs215189850	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77254998	TCTGCTTTTCACAAG[A/T]TGGGAGATAAACTCT	78514
rs215195386	snp	A/G			utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250577	AAGAAGTTTCTCTCT[A/G]CTTCCCTCCAGGTTG	78514
rs215195942	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77380927	CGACTGTGCAGACTG[-/AA]ACTCAAAACATCTGG	78514
rs215200826	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77263266	TGTTATTCCCACCCC[C/T]TTCTTTAAACCATCT	78514
rs215205602	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77430867	GAGAGGAGAGCAGGC[A/G]AGAAGCCAGGATGCT	78514
rs215207808	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77278513	CTAACATGGCCTTGA[C/T]TTTCCTGGTGATGGG	78514
rs215224267	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77439326	TACAGATCGCCTCCA[C/T]CCCAACAATGAGCGT	78514
rs215226974	in-del	-/TGGTCTTGTTGGAGTAGGTA			intron-variant	Arhgap10	Mm_Celera	8:77296023	CTGCTGGAGTAGGTG[-/TGGTCTTGTTGGAGTAGGTA]TGTCACTGTGGGTGT	78514
rs215244514	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77255541	CAGAGAAAGTCAAAG[A/G]GCAAGGCACTATAAA	78514
rs215250821	in-del	-/C			utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250902	CCACGATCAGTAGGA[-/C]CCCCCACGGCCGGGA	78514
rs215251542	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77369464	ACAAACAATGGGCAC[-/A]AAATATGTATGTCTT	78514
rs215251658	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77328175	TGCTGTGGATAATCC[G/T]GATTGACTCGGGATG	78514
rs215252569	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77287637	AAGGAATACTTTATA[C/T]CTCACATAGAAATGC	78514
rs215254333	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77254724	ATTACACTGTAGGAT[C/G]CCTGTTCTTGCTAGA	78514
rs215281085	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77423230	CTAGGAAGCGTAAGA[A/G]CAATAAGCCAGAAGA	78514
rs215281772	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77324709	CCCTAATACTCTTTT[-/C]CCCCCATAAGACAAC	78514
rs215291803	in-del	-/TGAT			intron-variant	Arhgap10	Mm_Celera	8:77510244	GTACTCTTAAAACAC[-/TGAT]TGATCCTCCTCAGGC	78514
rs215297819	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77272448	GACCCTACACAAACA[A/G]CTGAGGTGCATATTT	78514
rs215301845	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77336814	AGAGAAGTGAGGCAG[-/A]AGAGGCAGCAGCAAG	78514
rs215304700	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77398906	ACCCCCAATCCTCCC[A/C]AAAACCTTAAATGCT	78514
rs215313357	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77328609	TCTTAACCCACAGCC[A/C]CACCTACCTCCTACC	78514
rs215319896	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77407198	GGGCTGTAGAAATGA[C/T]TCATTGTTGAAAGTA	78514
rs215332267	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77272667	TCTTCCCACTCTCCT[C/T]TGTCTCTCTCCCCTT	78514
rs215333705	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77381736	GTGCATATGTATGTG[-/T]GCTAAAAGTCAGACA	78514
rs215342603	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77429410	TCCTACACGATCCAG[A/T]GCTCCACATCCAGCA	78514
rs215344070	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77422624	TTCTCCCAGAGCCAG[C/T]ATGTGTTGTAGTACA	78514
rs215350179	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77360689	AATCCTTTATAACTA[C/G]GACTAAATAATTCTG	78514
rs215355396	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77472323	ATTGAGCATTCTCTG[A/G]CCCAAGTAATATGAC	78514
rs215375235	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77437546	GACCCTTGGAGACAC[A/G]TGGAAAAACCCCTCA	78514
rs215381260	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77407700	ACTGGGTTACAGGAG[A/C]CTCAACAGAGGGAGG	78514
rs215382717	snp	C/T			intron-variant, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77517525	AATCGCCTATTCCTC[C/T]AGCCCGGTCTTAGGA	78514
rs215387262	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77386324	AGCCCTGGCTATCCT[A/G]GAAAACTATACAAGC	78514
rs215398874	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77428771	TGGGGTAAACAGCAA[A/C]TGAGGAGGGCGTGGC	78514
rs215417474	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77342281	AGAAAGAGAGCTGGG[A/G]AAGTGATGTAACTGT	78514
rs215423140	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77479016	AGCAGCCATTCACTC[C/G]CAGCCAGCCACTGGC	78514
rs215427217	in-del	-/AGCCCTTCACAC			intron-variant	Arhgap10	Mm_Celera	8:77327595	CACAGTGGCTCTGAA[-/AGCCCTTCACAC]AGCCCTGGGTTTAGG	78514
rs215432558	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77383163	AACCCACAAATGTGC[A/T]CGAAGGCTTTCAGTG	78514
rs215449029	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77450120	AAACCCAGTGGTAAT[C/G]AGACCAAGAGTCTGT	78514
rs215478297	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77491759	CCTGCAACATCAAAA[C/T]GGCACGGCCTAGGAG	78514
rs215478846	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77412909	TCAAGTGCTTTGTTA[G/T]AAGATACACAAGGAC	78514
rs215487415	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77260707	TTAACTGCTATGATG[A/G]ACACCACTGATAGAA	78514
rs215491052	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77383588	GAAAACTGAACGAAG[C/T]TTTCAAGAACCGACT	78514
rs215506423	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77455914	AATAACCCTATCTCC[C/T]CAAATTGTTTTATCC	78514
rs215507682	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77432873	GGCGTCTCATTTTCA[G/T]CTTGCACTCCACCCA	78514
rs215509479	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77449703	GAGATCCAAAGCATG[C/T]AGGAAGCTGGCTACA	78514
rs215511439	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77455345	TCAAGAAATGAGCCG[A/G]AGACACGGCCACAGG	78514
rs215516525	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77333223	GAAACATGGTTAAGA[A/G]TGGCTGTGAGCCACC	78514
rs215534338	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77491399	TTCTGTCCACACATC[G/T]TCACCACAATGAGTC	78514
rs215539784	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77369246	AGGTGTGCGCCACCA[C/T]ACCCGGTCATACTAG	78514
rs215542681	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77378267	AATTCTGAGCAAAGC[G/T]GTGAGAGTTCCAACC	78514
rs215554440	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77474804	GCAGGTCAAAGGTCA[A/C]TGACTGAGGTCATGG	78514
rs215566503	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77454925	TGCCCTTGATGACTT[C/T]ATTGAGAATAGTGAT	78514
rs215570422	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77333764	CTGAATGTACGCAGG[C/T]AATTTTCTGAAAATA	78514
rs215571171	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77359057	CTAACACTTGTATTC[C/T]TTACAGCAGTTCTCT	78514
rs215573460	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77324061	GAACGGCCTCCCTTG[C/T]GGCCTAGCAGTCTCC	78514
rs215576150	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77418432	AGGGTCTCAGGACAG[A/G]CTTAATGTCCTATGA	78514
rs215578418	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77336805	GGCAGGGAAAGAGAA[-/G]TGAGGCAGAAGAGGC	78514
rs215601133	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77440033	ACCCACAGAAATAAG[G/T]GATGAAGTTAGTCTC	78514
rs215605067	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77454022	CTCATCCTAGGCCCA[C/T]AGCCCATTCTCAACT	78514
rs215606244	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77447896	AGAGGTGACTGTGTG[C/T]CATACTGGGCATAGC	78514
rs215609218	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77258634	AGAAAGGGAGAGTAG[A/G]TTCCCACCAGGCTCT	78514
rs215619787	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77426643	GTGCGCTCGTGAGGT[-/C]TTTCCCAACCCTTAA	78514
rs215620089	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77359940	ATTGTAAACGATCCT[G/T]TAAACTCACGTGTGC	78514
rs215620304	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77352953	CTCCCTCACCCAAGT[A/G]CATGTCCTTTTCTTA	78514
rs215622374	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77406490	ACTCTACAGATCTGG[A/G]AAATGAGCTGGAGAA	78514
rs215626752	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77315285	CTTGGTTTATCCTTC[A/C]TGTACACCACAAGTA	78514
rs215636069	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77497231	AAGTGGGCACCAGAT[C/G]CCCTGGAATCAGCTA	78514
rs215639101	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77362529	TATGCTCTGAAAAAT[G/T]TACAAATTTGAAACA	78514
rs215650177	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77397476	ATTAAGGTAGCTTGA[G/T]AAAAATTATGCCTAC	78514
rs215653233	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77453563	GTGGGCAAGTGGAAC[C/G]GTGTCACAGACAGAA	78514
rs215654321	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77480710	CTGGAATGACACACT[C/T]GTGACTGCTGGGAAT	78514
rs215674634	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77353383	GGCAGGGAGACTGAC[A/G]CTGAAACATATGAAA	78514
rs215675227	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77347236	AAACATCAAAATAGC[A/G]GAAGCAAAAGGACTG	78514
rs215676538	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77315690	ACATATACTAGTGGC[C/G]TTCCTCACAGAGACA	78514
rs215678349	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77305762	AGAAGTACTGACACA[C/T]CGGTTTGTAGGAGGG	78514
rs215683167	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77253441	CAACTCTTTACCATC[C/T]AGCCACAGCAGTGAC	78514
rs215684755	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77504891	ACTGGGCTTGGCATG[A/G]GCCTTTGACATCGAA	78514
rs215697049	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77275203	CAGTAAAGTGTGTGT[C/T]CGTGCCTGTGTGTGT	78514
rs215710074	in-del	-/A			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77516412	TAAATTCTTCCCATT[-/A]AAAAAAATATTTCAA	78514
rs215710246	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77496856	TCAGAGATCTGTGTG[A/C]TCTGCCTCACAGGTG	78514
rs215712285	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77306922	AAGCAAGAAAGAAAT[C/T]TTCTTTCAACAAATC	78514
rs215714790	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77452908	CCCACACATAATCGG[A/G]GGCAAAATAGCAATG	78514
rs215720332	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77384164	TAAAGCCAGGAGCTT[A/C]TGAAGGACTTCTCAG	78514
rs215721737	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77253694	TGGTCCCACAAGTCT[A/G]TATGTCAACTTGCTT	78514
rs215736521	snp	A/G/T			intron-variant	Arhgap10	Mm_Celera	8:77511578	TTCATGTGGATGGAC[A/G/T]AACAGGCTACACTGC	78514
rs215739968	in-del	-/GC			intron-variant	Arhgap10	Mm_Celera	8:77328007	CTGTGGTCAGAAGCA[-/GC]AGTGGTATTTTTGCG	78514
rs215747829	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77384698	TAAAGACGGTGCACA[C/T]AGAACCAGCAACAGC	78514
rs215748315	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77340163	CATACACAGTTGGGC[C/T]GTTTGTTGGTTATGT	78514
rs215758268	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77478127	CTGATGTCATAAGAA[C/T]TGCCCAGACTACTGG	78514
rs215758874	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77275710	AGTCAGAGTACTTCG[A/C]AGGACATTTTCAAAT	78514
rs215774358	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77340723	TGAGAGCCACTAGTG[G/T]CACGCACACCCTGTC	78514
rs215774584	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77438507	ATTAAAATGGCCAGT[G/T]AAGTGCTCTTATTTT	78514
rs215774926	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77417552	TCAGTTTTATCATTT[C/T]AGTGTGGTTGGTATT	78514
rs215780964	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77332203	ACTCTGCTGGCTGGT[C/G]AGCCATTTTTAAACT	78514
rs215788921	in-del	-/GATG			intron-variant	Arhgap10	Mm_Celera	8:77374750	TGAGGCTCACATGCA[-/GATG]GACAATTGTCCCTAC	78514
rs215789198	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77372772	CATCTCCTTGAGCTC[A/G]CTGTGGTAAACAGTT	78514
rs215800463	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77288327	AAATTCTGTGGACGG[A/T]GGGACATTCCTCAAC	78514
rs215813898	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77410061	ATTTGGTCATCTGGA[C/G]CCGAAAATGGAAGCT	78514
rs215817181	in-del	-/GT			intron-variant	Arhgap10	Mm_Celera	8:77347972	TGTGTGTGTGGGTGC[-/GT]GTGTGTGTGTGTGTG	78514
rs215819105	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77477528	AGGTCTCTAATGGGA[A/T]AGGAAATCTAAAAGG	78514
rs215819981	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77479565	TCAGAGGTGTGACCT[C/T]AGTGGGGACAGCATC	78514
rs215823695	snp	G/T			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77516718	CAATAACTCAAGGAA[G/T]GAATTCAGGGTTCCA	78514
rs215828543	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77411693	TCAATCCCCAGATGC[C/T]ACAACGGAAAGAGAG	78514
rs215849216	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77444896	CTGACCTCTCCAGGA[C/T]CCCCACTGCCTCTGG	78514
rs215849837	snp	C/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503771	AAGTCACTTCAGGCA[C/G]GAGCTACCCATTACT	78514
rs215855881	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77260709	AACTGCTATGATGAA[-/C]ACCACTGATAGAAAG	78514
rs215863351	snp	A/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77366939	ACCTGTGTTTAATTC[A/G/T]TTTTTACCTTTATTT	78514
rs215873967	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77466325	TAAAAGAGGTCTGTG[C/T]CGCCAGACTTTGGGG	78514
rs215874870	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77476799	ACCTTTGCACCAGAT[C/T]GCTCACCTTTTTGCT	78514
rs215883570	in-del	-/C			intron-variant	Arhgap10	GRCm38.p3	8:77371906	ATCCCATGCCTACTT[-/C]CCAACCCAGCACGAG	78514
rs215884475	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77271440	GATGTTTGGCTATGG[A/G]GCTCTGTAGGGTATG	78514
rs215909895	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485477	CAAGCACTTCCTCTT[C/T]CGTCTCTGCCTTCAG	78514
rs215913463	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77266564	TAGCGGTCTGTGTAA[A/G]AAGGGAAAGTCAGTG	78514
rs215916567	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77280146	AACAGCTGTGGTGAG[A/G]AGCAGGTTTGAGGAG	78514
rs215917526	in-del	-/GAACTTA			intron-variant	Arhgap10	Mm_Celera	8:77441563	CGCTTTATTATATGT[-/GAACTTA]GAACTTATATTTCAG	78514
rs215922247	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77509736	ATTCTATAGAATATC[C/T]ACTGTACACTTGCAG	78514
rs215949223	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77316440	CTCTCATAGACTAGA[G/T]AGTAACGCCCAGCTG	78514
rs215964208	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77418986	CCAGTTGGGAATGGG[G/T]ATCAGTCTATAATCT	78514
rs215967817	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77499810	TTATGTCTAATAGAG[C/T]CCCTCACCAGATGAG	78514
rs215968206	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77475959	AGGCTATGTAAATGA[A/G]TGGAGTAAAACTGAA	78514
rs215976996	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77298337	ATCTGAGAGGAGTTA[A/G]GGTTAAGAGAAAACA	78514
rs215977772	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77267112	GCTCTTTCCCACAGG[A/C]CCTTCTGAAGGAGGG	78514
rs215986860	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77381475	CTCGTATTACGTCGA[C/T]GAGACACTAACCTGC	78514
rs215989101	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77317091	TTAGTGAGAACACAC[C/T]TGCTTGCTTCTTGTT	78514
rs215992854	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77462638	TTAGCATACAGAATG[A/C]TAGCTTTCACTGTGG	78514
rs215997261	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77434092	TTTTAAATCTGAATG[C/T]TCTACATTTAGCACC	78514
rs216025708	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77261337	CTCTCTGCTCTATGC[C/T]ACACTGCTAACATGG	78514
rs216028435	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77369529	ACAGAAATCTAAGCT[-/A]AAAAAGTTAAAGTAT	78514
rs216038331	in-del	-/AAGTA			intron-variant	Arhgap10	Mm_Celera	8:77430469	ATGAAGCAGGCCTCG[-/AAGTA]AACTCCCACCAGCAC	78514
rs216040714	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77381913	CTTCCAAAGAATGAG[A/C]TGAATTGTATCCCAT	78514
rs216043281	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77293000	GTCGATCCTATCACT[A/G]TAAAAATGAGTTAAA	78514
rs216045900	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77505502	TGTGGTGCCGGGTAT[A/C]GTGTCGCACATCTTT	78514
rs216048306	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77337364	GAAGAGAAACCTCTG[A/G]AGACTTCGCAGCTTT	78514
rs216053063	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77497911	TAATCTTCCATTATC[-/A]ATTTGGCTGGACTTG	78514
rs216062209	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77338772	AGCATGATCATCACA[A/G]ATGATCTCTATTTCT	78514
rs216087668	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77285682	GTCGTGCTGACTGTG[A/G]AAGCAAGTGACAGTT	78514
rs216097571	in-del	-/AT			intron-variant	Arhgap10	Mm_Celera	8:77448163	AAGGAAGTTGTGCGC[-/AT]GCGCGCGCGCACACA	78514
rs216103097	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77375842	ACATTCAAGCTGAGC[C/T]GCTAGTGAGGCCCCG	78514
rs216103201	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77382245	ATATACACACAGAAG[A/G]GACATGTATGCACAC	78514
rs216103247	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77284134	CAGAGACAGAAAGGA[A/C]ATATTCAGGGGTCAG	78514
rs216105523	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77331857	ACTCAGCCTGTCAGC[A/G]TGTGAGCACAGGCTT	78514
rs216113336	in-del	-/AAAAAG			intron-variant	Arhgap10	Mm_Celera	8:77402698	TATGACAAAAAAAAA[-/AAAAAG]AAAGAAAAAGAGTGA	78514
rs216136525	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77372694	CACACTGTCCCTCTG[-/A]CTCTTCCTTCCCAGT	78514
rs216141611	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77356878	ATATGACTTGATCTG[A/G]CCCTAACAAAGGCTA	78514
rs216146757	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77489443	TAAGTGCCATTGAGG[-/A]ACTTTGTAAATAACA	78514
rs216163257	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77397964	CCAGCCACTTCTAGC[A/G]CCTACCACTGTCTTC	78514
rs216173285	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77404931	CCACCAAGCCTGGCT[C/G]CAGAAACCTATTCTC	78514
rs216183844	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77319628	CTTCTCTCCACATCT[C/T]CACAGGCCCAGAACA	78514
rs216185685	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77348034	GTGTGTGTGCCTCAT[A/G]CACATACCTGTCTTT	78514
rs216189873	in-del	-/C			intron-variant	Arhgap10	GRCm38.p3	8:77506164	GCTGTGGCTTGTGAA[-/C]GGATGAAAGTAGTCT	78514
rs216191964	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77287916	AAAGAGAAAGAGAAA[-/G]AAAAAGGGAAAGAGA	78514
rs216192983	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77293791	CTAAAAAGTAGGAGG[G/T]CTCATGAGTTTGTTG	78514
rs216194024	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77483385	GAGAAAAGGAGGAGA[A/G]GGACTGAGAGAAGGG	78514
rs216199053	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77357404	CAGTAAAATGTGGAT[C/T]CTCACGCACTCATGG	78514
rs216207136	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77501844	GTTTGGATCATAAAT[A/G]CCCCCCAAGATCACC	78514
rs216207558	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77428051	CAATGGCAAGGAGCA[A/C]TTGTTTCTTATGAAG	78514
rs216207609	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77349633	TACCAACACTCAAAA[-/G]GGGGCTCATTTTGAA	78514
rs216208317	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77504309	CAAAACCTTCTGTAA[A/G]TCTTTTTTAGGAGAA	78514
rs216223804	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77470908	GAGCTGCCGTGTGGG[C/T]TCTAGGAACTGAGCC	78514
rs216227848	in-del	-/TCAGC			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493687	TGGCTGAAATGTTGG[-/TCAGC]AAAGCTATCTGTTAC	78514
rs216247329	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77288496	TCTTCCAAGTTGCTC[A/C]CTTCCTGGTTGTACA	78514
rs216250444	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77265663	TCAGGCAGGGCTGGG[C/G]TTAGGGTGGCCATGA	78514
rs216252987	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77313481	TAGACTCAAACAGTT[A/G]TTTGTTGTAGGAGCA	78514
rs216256434	snp	C/T			intron-variant, downstream-variant-500B	Arhgap10	Mm_Celera	8:77358164	CTTTCTCTCTCTCTC[C/T]CTCCACTACGCCCTA	78514
rs216263711	snp	C/T			synonymous-codon	Arhgap10	Mm_Celera	8:77257363	TTCAAATGACAATTC[C/T]GAGCTGTGTTCTGCT	78514
rs216272392	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77427742	CACCTGCAGGACACT[A/C]CACCGGCAGCCCCAG	78514
rs216277650	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77470672	GACCCCGAGAATTTA[C/G]TTTCGAATGGTAGTG	78514
rs216297563	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77257838	CAGCCATGCCTTCTC[G/T]GTCTTTAGACCTTTC	78514
rs216301343	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77373071	TAATGGTCTTTTTTT[G/T]GGGAAGGGCAGAAGA	78514
rs216306783	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77252454	TATTCTTAAAGGTTC[C/T]ATCCATACATTGTAG	78514
rs216311980	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77314228	CAACGTGTAGGAATG[C/G]TGTTAAATTATATCC	78514
rs216316255	in-del	-/ACT			intron-variant	Arhgap10	Mm_Celera	8:77506104	CCCCGCCTCTAGAAC[-/ACT]GCTGACATTACCGAC	78514
rs216328672	in-del	-/TT			intron-variant	Arhgap10	GRCm38.p3	8:77473289	ATTCACGCACGGTTA[-/TT]TTTTTTTTTCCAAAA	78514
rs216331361	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77434710	ATCACAAACAGCCAC[C/T]TTAACCAAACCCGCA	78514
rs216331596	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77427143	TGCCACAGATGCATA[C/G]AGCACTGAACAGAAG	78514
rs216339426	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77268440	GGAGTCTCAAGCAGC[-/A]AAAAAACGCTACCCC	78514
rs216354276	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77452309	AGAATGCAGCCTCAC[-/T]TTTTTTTTGTTGTTT	78514
rs216355365	in-del	-/AAAGAAAG			intron-variant	Arhgap10	Mm_Celera	8:77316276	ATTTACAAGTTTAAA[-/AAAGAAAG]AAAGAAAGAAAGAAA	78514
rs216364415	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77401317	ACAGAAACTGAAAGC[C/T]TGTCTCTCTGAAACC	78514
rs216364462	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503141	GCCAAGTTTTAATAA[A/G]ATAAACCTGGCAAGT	78514
rs216375059	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77388594	AAAGAAAAATGACAT[-/G]GGGATGAAGCAAGCC	78514
rs216377475	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77367705	CCTAAGGATTTTAGG[C/T]CCCCCCTCCCCCCTG	78514
rs216382454	snp	C/T			synonymous-codon	Arhgap10	Mm_Celera	8:77426333	TGTCAGGAATACCTC[C/T]TGCAAGTGTGAGTCC	78514
rs216386311	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77465296	TCCAGAAATAGGAGG[A/G]AAACTGTGGGATGTC	78514
rs216389975	in-del	-/A			intron-variant	Arhgap10	GRCm38.p3	8:77481811	GGAAGTCTCTATGTG[-/A]ATTTCCCAGAATTTC	78514
rs216401832	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77323030	CTCCCGACTGGTTCG[C/T]TCAGAAGCTGCAAGC	78514
rs216405850	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77415750	TAATCAGAAGGACAC[C/T]AAACACTGAATTTGG	78514
rs216418898	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77274047	AAGGTAAAGAGAAAA[A/G]AGGGTCCGTGAGCTG	78514
rs216419473	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77508989	AAGACTTTCTTAATT[A/T]AATATATATATACAC	78514
rs216436402	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77331132	AAGGGGGCAGACATA[C/T]GCACTTTTGTGCAAT	78514
rs216440305	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77396152	GCAAGTTCATTATTA[C/T]TCAGTGAAAGAAGTC	78514
rs216441283	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77505624	ACACTGTGAGACCCT[G/T]TCTCAAGAATAACAA	78514
rs216441926	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77432689	AGTGTACAGCAACAG[C/T]AGAGACATAGGCATG	78514
rs216452505	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77274572	TAAGAAAAGAAAAAT[A/G]CAATCAGTCCAGGTT	78514
rs216457517	in-del	-/CCCCCCCCCCCCCCC			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	GRCm38.p3	8:77515753	GAGGAGGAAAACTAG[-/CCCCCCCCCCCCCCC]CCACACACACACACA	78514
rs216459404	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77363086	CGTCCTAACGTGCCT[C/G]TGTCCGGACTTCTCT	78514
rs216466353	in-del	-/ATAGAC			intron-variant	Arhgap10	Mm_Celera	8:77467949	AAGGCAAGTACAACT[-/ATAGAC]AGTGACACAGACACA	78514
rs216475531	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77474728	CACAGTTTTGCTGAG[G/T]TTCAGTGGAGTTCAA	78514
rs216500693	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77386967	AAAAAGAAAGAAAGA[A/G]AGAAAGAAAGAAAGA	78514
rs216502666	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77409474	GTTCAGAGAAATCAC[A/G]CTGGCCACTCATTTT	78514
rs216505267	in-del	-/AAGTT			intron-variant	Arhgap10	Mm_Celera	8:77420380	CAGAAAATTATGAAC[-/AAGTT]AAGTTGTGAGTTCAA	78514
rs216505526	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77431682	AGCATCCAGAGCCTG[A/C]AGCTCATTGGCTGTC	78514
rs216507252	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77319289	CAGACAGCATCAGAT[A/G]AACTTACTCTATCTC	78514
rs216521040	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77456370	CACTGTAGCTACAAG[-/T]AAGTAAATAACTCAT	78514
rs216522326	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77346260	GAGAGCTGATGGGGA[A/G]GGAACACTCACTTGG	78514
rs216541105	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77436190	AAAGTTTCCGATGGT[C/G]TTTCCATTATGACTG	78514
rs216545898	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77293644	CCTACATGAAAAGCT[A/T]TAAGTGATTAACAAC	78514
rs216554859	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77452467	TAAAGGTGTGCACCA[A/C]CGCTTTTAACAACTC	78514
rs216561145	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77341632	CTTGCACACTCCCCT[C/T]AGGCTGGGCACTGAC	78514
rs216575732	in-del	-/AGG			intron-variant	Arhgap10	Mm_Celera	8:77300147	GAAGAAGAAAGATGA[-/AGG]AGGAGGAGGAGGAGG	78514
rs216594170	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77326459	AAATAAAATATATAT[A/G]TGTGTGTGTGTGTGC	78514
rs216614207	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77451786	GAATTAAAGTGGTCT[A/G]CGGCGGCCCATGTGA	78514
rs216618123	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77380357	TGGCAACAAGTGTTG[C/G]ATAAGACATAAGTTT	78514
rs216618184	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77386168	CATGGTGGTATTTTT[G/T]CTATGCAAATTCACT	78514
rs216619107	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77335768	AGATGCAAATAAATA[A/C]ATAAATGAAAAGGAA	78514
rs216636078	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77342166	CAAGGAAGGGACCAA[C/G]GGATCATAGAGAGCC	78514
rs216645527	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77500838	CCCACCAGCCACATA[C/T]TAAACACTATCATTC	78514
rs216645875	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494381	CAGCAACACAGCTGA[A/G]CAACTCAGCAAGACC	78514
rs216647738	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77365450	ACAGGTGCACTTCCA[C/T]GGTTTTGTTTATTTA	78514
rs216657726	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77286392	TTCAATATTGTCTTA[A/G]TCACCATTCTATTCT	78514
rs216660162	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77460714	TCCAGAGGTTAGAAC[A/T]AGCACTCTGCACGTT	78514
rs216661478	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77414144	AGGAGGAGTAAGGTC[C/T]CACGGGCAGATAATG	78514
rs216674750	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77380757	AGACTATCAACTGCA[A/T]TTAAGACTCCGCCGA	78514
rs216678705	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77408477	ACATCTGCAAGGTCT[-/C]CAGGGCCTCCCTGAA	78514
rs216680081	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77281186	CCTCCACCAAATACT[A/C]GCCAACACCTGTTTG	78514
rs216691410	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77336240	TCATGAAAACTGTGT[A/G]ATTTATTTTCAAGAC	78514
rs216692576	in-del	-/GCCCATCA			intron-variant	Arhgap10	Mm_Celera	8:77345657	ACAGCAGACAGGAGT[-/GCCCATCA]GCCCATCAGCCCTTC	78514
rs216698872	in-del	-/TCCT			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77504150	CTTGTTCATCCCTCC[-/TCCT]TCCTGGTAACCTCAG	78514
rs216713272	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77361999	CAAGGCTCGGGGGAG[C/T]GGAAACAGATGACAC	78514
rs216715355	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77369216	CTGCCTCTGCCTCCC[A/G]AGTGCTGGGATTAAA	78514
rs216719491	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77482926	GAATCACAAGCCATC[A/G]ATAATATTTTAGTAA	78514
rs216726657	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77366038	TTACAGCTTTCTCCG[C/T]GCTTGCTTTCTGCAC	78514
rs216735230	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77408696	ACGCATTCTTTCTCC[C/T]GCGATCTTGGCAAAC	78514
rs216737248	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77317587	CTGACTGGACTCCTT[A/C]AAGCAGAACCACACC	78514
rs216755868	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77262775	CCTAAACTGTTCACA[C/T]ATATGCAGGCCGCTC	78514
rs216757333	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77370424	ATTTGCCATTTCTCT[A/G]AAGTAGAGAAAAAGA	78514
rs216763870	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77412765	CAGCAGGCTATCTCA[A/G]GTGAAGCCCTTATAC	78514
rs216769300	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77362419	GTCTCAAGTAAATAT[A/T]GCCTTCTTCTAAAAA	78514
rs216775065	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77400865	AAGGCCGTGACTCCT[C/G]GCTTGGCTAAGCTGA	78514
rs216781080	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77265908	AACATTTCATGACAC[A/G]TGCTGCAAGACAAGC	78514
rs216786974	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77344224	CCAGGTATTTTATCA[C/T]CACAGAAGGGTGACC	78514
rs216793381	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77318313	TACATAATGGAACTC[A/G]GCTTCTGGGATTCTC	78514
rs216796664	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77441217	AGCAAGACCGTCCAC[A/C]GGCGTGAGCCTCCTT	78514
rs216797680	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77311154	TCTCATGAGGCAGAC[A/G]AAACCGCAACCCTTC	78514
rs216801444	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77513830	CCGGAAGGGAACATT[C/T]ACGAGTATGAGAACT	78514
rs216810230	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77499329	CCTTTTAAAAGGGCA[A/G]TGGTGGCCCACACCT	78514
rs216820007	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77291272	GAGAAATGTGAAGAG[G/T]GGTGAAGGGCAAGGG	78514
rs216822214	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77482017	CGCTCCCAGAGCAGA[C/T]TCCGCAGCCTCAGGG	78514
rs216830516	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77263184	TTTTAATACTTAATT[C/T]TTTCAAATGCCCTAC	78514
rs216833259	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77311771	ACCGGCACGCTCCTC[A/G]GGTGGAGACAAGAAG	78514
rs216849731	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77498994	CCCTGCTCCCTGCCC[C/G]CTGCCCGCTGCCCGC	78514
rs216851805	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77461308	CATGGTTTAACAGAG[A/G]GTTTAGCTGTCAGCT	78514
rs216859832	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77455478	ACTTCTACTCTCAAC[C/T]TCTGGAGCCCCTGTA	78514
rs216862145	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77255465	AAGTCCTCTATATCT[C/T]GCTAATACATCCTTT	78514
rs216866004	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77271206	CCTTGTGGGTGGTAC[C/T]ATCCCTGGGCTGGTA	78514
rs216867490	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77504818	GAGCATGGCACACTG[G/T]CCAGCATGGCCTTGG	78514
rs216878395	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77288119	GTGCCACATCCCAAA[A/G]CAGTCACTACAAAGC	78514
rs216879458	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77279300	GAAAGAAGGACTGGC[A/G]CTTCCTGTGCTTAGC	78514
rs216885013	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77447391	CAGTCTCTAGGAACC[A/G]AGAAATCTCCATCGG	78514
rs216889087	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77259710	CACTGATTACTCTTC[C/T]GGAGGTTCTGAGTTC	78514
rs216897218	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77474250	AGATTATTTGCTTCC[G/T]TTTAAGCTACTTTTC	78514
rs216926436	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77412213	GAGACTGACTGGATG[A/T]TGGGGCACCACCCCA	78514
rs216928002	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77439219	GAAAATCAGCTAAGG[A/T]CTGAGGTCAACGGTG	78514
rs216930499	in-del	-/GC			intron-variant	Arhgap10	GRCm38.p3	8:77460985	CTGGCCTACAACACA[-/GC]ACAAAGACAGAGGGG	78514
rs216945530	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77459869	GACACTGCTCCCAAA[C/T]GGTTGGAGCATAATA	78514
rs216951523	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77335279	CCCTGGCAAATCAAA[-/G]GAGGTGAAAAAAACT	78514
rs216956004	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77480136	GTCCTTGGGGCCTCC[A/G]TCCTTAGGGCCAGGC	78514
rs216958921	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77284903	GAGAAGACAATGATT[C/T]AGAGATGCACAATAC	78514
rs216963323	in-del	-/GGGGGA			intron-variant	Arhgap10	Mm_Celera	8:77512454	TGAGACCTCGACTGC[-/GGGGGA]GGGGGAGGGGTCCAC	78514
rs216972600	in-del	-/AAAT			intron-variant	Arhgap10	Mm_Celera	8:77417641	TCTGCCCTTATTTAA[-/AAAT]AAAAAATTAAAAACC	78514
rs216979156	in-del	-/ACAAAAAACAAAAAAC			intron-variant	Arhgap10	Mm_Celera	8:77284402	TCCAGCGAGGGGGAA[-/ACAAAAAACAAAAAAC]AAAAAAACGCAAAGG	78514
rs216984063	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77438625	GTGTGCCCTGCCACC[A/G]AGACCGTCAGAAAGC	78514
rs217000256	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77325972	AGCCCGTGCTCACTG[C/T]TCTTCTTTTCTGTAT	78514
rs217008708	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77479805	GCAACTGGTGACCAC[C/T]CAACCTTGGCCTTTC	78514
rs217024725	in-del	-/CA			intron-variant	Arhgap10	Mm_Celera	8:77433459	ACACACACATCTGGC[-/CA]CAGTCTCATTCATGG	78514
rs217033773	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77408224	TCAGTGTCTCCAAAA[A/G]TAGGAGCTTCAGAAA	78514
rs217034673	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77421770	TTGAAAGCAGTGGTT[A/G]GCTCACGTGACGCTC	78514
rs217037252	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77462804	TTTTGGAGGCCTGGC[-/T]TTTTTTTTTCTCTCC	78514
rs217041205	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77270270	AAATGCCAAGTAGTC[A/G]CCCCTGAGGAACCTC	78514
rs217043826	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77451003	TAGAACAAGAATGGT[A/G]CTCCACTAAGAACTC	78514
rs217052400	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77284842	TTTATAGGTAATGGG[-/A]CACAGCTAAGCAGGA	78514
rs217062406	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77465670	TCTGCCCAGCACCCA[-/G]GGTATCTTACCAGGC	78514
rs217062880	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77478778	CAGTGGTCACTGGTC[G/T]CGAGCCTAGGAGGCC	78514
rs217063838	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77464743	ATTTAACCTGACTTC[A/C]AAAATGCCTTACCTA	78514
rs217064902	in-del	-/CA			intron-variant	Arhgap10	Mm_Celera	8:77279043	GCAGAGAAAGTGGGG[-/CA]CACTAGACTGAGCAG	78514
rs217067757	in-del	-/GCAGTG			intron-variant	Arhgap10	Mm_Celera	8:77316569	CAGTCCATGGCATCA[-/GCAGTG]GCTATAATACCTTGC	78514
rs217068568	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77271103	AAGCTGGAGTTATTA[C/G]GGAGAAAGGAGCCTC	78514
rs217080036	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77383728	GGAAGACCAGGAAGA[A/G]GGAGAGGAATGTAAG	78514
rs217083239	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77397174	ACTTCTCATGAGATT[A/C]CTGGGGCTTCTTGCC	78514
rs217099480	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77264539	TCTCAAACTCAGGAG[C/T]GTATTCCTGAGAACA	78514
rs217102729	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77436786	TCTCCCATGACCTTC[A/C]AGACACTTCCAATTT	78514
rs217116528	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77254498	TCTTTTTTAAAAAGA[A/G]GGAAGGGGGAAGGGA	78514
rs217118005	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77478266	AGAACACTCCCAAGT[A/G]TACAGCGAGGAGGGA	78514
rs217118692	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77339402	GAGAGGCGCTCGACT[C/T]TTATGTTATATGGCA	78514
rs217123403	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77286547	AGTAGCTGGAAGCTC[G/T]CACATTGAGAGGGAG	78514
rs217123450	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484801	GACTGTCTCACAAAA[A/G]GGGGAAGAAGGGGAC	78514
rs217133535	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77384085	TGCTTTAGCTGCAAG[A/G]CCAGAGAGTTTCAAG	78514
rs217158211	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77340019	TCTCAGTCCAAGCCC[-/A]AAACACTGCCATCTG	78514
rs217161719	snp	G/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484247	ACCCATGTCAGGGAC[G/T]GAACACGGGGCCTCA	78514
rs217176188	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77287484	GCCTACTGGCAGGAA[A/C]GCATTTCCATGTCTT	78514
rs217182917	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77442146	AGAGCTGGTGCAGAC[C/G]GCTGAGACAATGTGT	78514
rs217189342	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77340041	TGCCATCTGGCTGTG[A/T]CCCCATGAACAAGTT	78514
rs217201626	in-del	-/ACACACGTGT			intron-variant	Arhgap10	Mm_Celera	8:77411379	AATACATACACGTGC[-/ACACACGTGT]ACACACAGACACACG	78514
rs217207395	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77266033	CAGCGACCTGAGCTC[A/T]GAGGACTCAGGAGGC	78514
rs217210005	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77366926	ATTTCTAGTTCCAAC[C/T]TGTGTTTAATTCTTT	78514
rs217216571	in-del	-/AGA			intron-variant	Arhgap10	Mm_Celera	8:77255188	AGACGCAGGGCTCAC[-/AGA]AGATGAGGCATCCAC	78514
rs217234468	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77259941	GAACAGGGTTAGATT[A/G]GATGAACAAATGGAT	78514
rs217234489	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77504531	GTCTTCCCTGTGACT[C/G]TCAGCAACTGTCTTA	78514
rs217244386	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77290661	TGTGATGACTCCCCC[C/G]ACCCAACCATAAAAT	78514
rs217249324	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77334386	TGGAGTCCATGGAGA[A/G]CAGTGCAGTAGAGTT	78514
rs217255907	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77338696	ACAAAACAAATAAAC[-/A]AAAAACAGAGCATAG	78514
rs217256984	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77360591	TGATCAGTCCCTACA[A/G]CAGAACTCATTTGTT	78514
rs217258491	in-del	-/AT			intron-variant	Arhgap10	Mm_Celera	8:77489506	GAGGAGAACACACAC[-/AT]ACACACAAACACACA	78514
rs217282542	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77322432	TAAGGAGATGTAGGC[C/T]AGGGGTTGACTCCCT	78514
rs217291197	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77322083	CAGCTGGCCTCTCTC[C/T]GCTTCCACAGCCAAC	78514
rs217293571	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77315861	ATACAAGAGTATATG[A/G]GAGGTTATATGGAAA	78514
rs217297757	in-del	-/TCTT			intron-variant	Arhgap10	Mm_Celera	8:77318135	AATAAAGCTTCTCTC[-/TCTT]GCTTAACTTGGTCTT	78514
rs217300853	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77260482	AATACAATTCCCAGT[A/G]CCTGCAAAGTGGCTC	78514
rs217318604	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77396572	AACACATGAACACAC[A/G]AATTGAACAAGGTTC	78514
rs217326583	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77261175	GTTCACCTTGACAGT[C/G]CTCTTCATCATCATC	78514
rs217351084	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77440711	TCCGGTTTCGGAGGA[C/T]CCATCGCCCCCTGCT	78514
rs217351362	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77316304	AAGAAAGAAAAAACA[A/G]ATTTTGTTAAGCAGA	78514
rs217367805	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77415034	TTTACATTGGCATTA[-/T]TCATTGCGGTAAGAT	78514
rs217367906	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77430165	TTAAATGTTTGCGTC[A/T]ACTGGGTACCATCAA	78514
rs217415659	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77447089	GTGGTTGATTTTTTT[C/G]TTTGTTTGTTTTGGG	78514
rs217419272	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77352021	CATCTTTAAAATATT[A/G]ATATCAAAAGAATAC	78514
rs217425700	snp	A/G/T			intron-variant	Arhgap10	Mm_Celera	8:77436076	AAGCATTGGAGCCTC[A/G/T]AAGTCCATCCCCAGA	78514
rs217430945	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77437477	TGGCCAAATCACCAA[G/T]CTCTGGGCCAGTGAG	78514
rs217433147	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77344291	TTATTTCTCTGAGCT[-/A]AAAAAGCCCTCTCTT	78514
rs217444697	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77415315	TCGATGGAAGGAGGC[A/G]TCTAACTCTGTACCA	78514
rs217446075	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77285651	AGGGGAAAATGAGAG[A/G]AAGCTGAGACTATTT	78514
rs217454066	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77263766	CCGGAGTCCTCTCCA[A/T]TACTTCACAGCTATT	78514
rs217467828	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77435459	TCTGGATCTAAACAG[C/T]CTCCAAAGGTCCACA	78514
rs217470202	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77458984	ACATGGTCAGGTTTT[C/G]GGGGGCAAATGCGTG	78514
rs217498247	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77317979	GGTGGCATCATTCCA[C/T]GGTCTGGGAGAAAGC	78514
rs217501089	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77454905	CCAGCACAACAGCCA[C/T]AGCGTGCCCTTGATG	78514
rs217507536	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77421442	AGGCACAAAGGTCTG[G/T]AGACTGGTGGGGAAC	78514
rs217531375	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77464385	TAATTACCGTGTGGA[C/T]ATTCTTTGAAGTAGA	78514
rs217554059	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77508131	AGTCTTTCTAGCTGG[G/T]TTTTTTTTTTTTTTT	78514
rs217554587	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77399692	ACAAGACCCAGTGGC[C/T]CTTGAGCAACTCTCT	78514
rs217556371	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77454164	CAGCTAGCATTTCGC[A/C]TCCCGGAGCAGCATC	78514
rs217559018	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77411003	ATATAAAACAAAATA[A/G]CTCCTATCAAATACT	78514
rs217565849	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77270056	CAGGCACTCAGAAGA[-/G]GGCCAGCAAAGGACA	78514
rs217566945	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77419326	AGAGAGACAGAAGTG[A/G]GCAGCCTCTGGCCTG	78514
rs217571340	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77511077	TAGTAAGTATGAAAA[-/G]GCTAGAGGACCGGTC	78514
rs217574179	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77338257	ACTCTGAGTAAAACA[A/C]CACAGTACTGATATC	78514
rs217574296	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77345453	GTCATATTGCTTGTC[A/G]TTTCAACAAGTGTGT	78514
rs217589475	in-del	-/ATGCTGCAACAGTCCCACTCTCCTCGTATCAACACCAGGCACA			intron-variant	Arhgap10	Mm_Celera	8:77422801	TCAACACCAGGCACG[lengthTooLong]CTGCTGCAACAGCCC	78514
rs217591719	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77477416	CGACCGAAGACTCCC[C/G]CATGTCACTTGAATC	78514
rs217592251	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77462697	AGCCACCCCTCTCTA[C/G]CCTTCCACTACCACC	78514
rs217599724	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77297593	TAAGAGAACACAGCA[A/G]TAAAGTGACTAACAG	78514
rs217611089	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77460173	AAAGGAGTCGGGGGT[G/T]GGGGAGCACAGGTGG	78514
rs217615127	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77514375	ACATCGCTGAGCTCT[A/G]AAACGCCAGGGATCT	78514
rs217631229	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77411543	ACACATAGACACATG[C/T]ACACACATGTACACA	78514
rs217631360	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77321559	CAGTCTTCATTTCCA[A/G]GAAATGCCCAGTCAC	78514
rs217632010	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77338616	TTCCAGTTGTCCTCC[G/T]TTGTTCTTTATGATT	78514
rs217632276	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77343248	CCAGTATCTCTGCTT[C/T]GTCCCAGGACCTGCT	78514
rs217645060	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77443357	GGGAAGCCCACAGTT[-/AA]AAAGAGTATATGATC	78514
rs217648644	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77420025	GAGTAGAAAAAGAGC[C/T]GCACCCCAAACATCT	78514
rs217659738	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77374841	AGACAGACAGTTGTC[C/T]CTACTGCAGCTGAGG	78514
rs217667535	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77425831	AGGCTCACACAGTCC[A/G]ATTCATCAAGACAAC	78514
rs217669511	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77440364	TCCCTTAGATGGCTA[C/T]AAGCTAAGCACCTGT	78514
rs217676175	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77462985	AGCACAGCGACTAGA[C/T]AAATCAGCATGTTTT	78514
rs217690571	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77468284	TGCTGTGGGGCCACC[C/T]ATGCCTCTAAACTCA	78514
rs217706887	in-del	-/CAGCAGGCTCT			intron-variant	Arhgap10	Mm_Celera	8:77496437	AGCCTACTCTGGCTG[-/CAGCAGGCTCT]CATTCGCCTGTCCTC	78514
rs217709842	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77506040	CTCAAATGTACTTCA[G/T]AGACAAGGGTGATCT	78514
rs217716247	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77292174	CAGGCTTAAAGAAAA[A/G]CAAAAATGTAAACAT	78514
rs217719467	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77330752	AAAGTACAAGAGGAG[A/G]CAGATGCAGGGAGTA	78514
rs217721266	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77512462	CGACTGCGGGGGAGG[A/G]GGAGGGGTCCACAGT	78514
rs217728877	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77382441	AACCGTGAGGATACA[C/T]TTCCACTTGGGCCAT	78514
rs217729175	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77396017	TCTATACAAGATTTA[C/T]TCACAGCCTCTGCAA	78514
rs217753179	snp	A/G/T			intron-variant	Arhgap10	Mm_Celera	8:77370038	GAAACCAGCAAAGAC[A/G/T]GGAGTGGCTGTGCAC	78514
rs217759083	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503690	CACGGTTCTGACGGA[C/T]GTCAATGGCGCTGGC	78514
rs217759147	in-del	-/AGTG			intron-variant	Arhgap10	Mm_Celera	8:77353195	TCCAAAGCGGAATGC[-/AGTG]AGTGCTGAGCAGATA	78514
rs217760934	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77469401	CAAAACACTCTTTGC[A/G]TTTACATCCTATTTG	78514
rs217763793	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77343650	TTTGCCCCAACCAAA[A/G]TTGCTTTTTGGTTAG	78514
rs217776393	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77470321	TTGTGACTTGTTTTC[-/A]TTCACTCATTGTTCA	78514
rs217784576	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77513097	CAAGCACTCTACCAA[C/G]GAAGCTATTTCCCCA	78514
rs217793474	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77285242	TCCAATATATACGCG[C/T]GTGCGTGCGTGCGTG	78514
rs217797378	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77324748	ATAACTTAAACTGAA[A/G]AAAAAAAATTCTAAG	78514
rs217799447	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77269658	GAGAGCTACTACTAC[C/T]ACCCTTGCCTAGTAT	78514
rs217810974	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77398848	GTCAAGTGCCTTTTA[C/G]AGAAAGGACAATAAA	78514
rs217814912	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77502927	ACCCGCTAAGGGAAA[A/G]CACGCCAGTAAGGTC	78514
rs217822943	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77481548	AATACACTGCTAATC[C/T]CAGCCTTTGGAAAGC	78514
rs217824183	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77463986	AAAAGGGGAGATTTA[C/T]AATAAACATGTATTA	78514
rs217827077	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77415677	CATCAATTAATAGAC[-/A]TACCTACAACCTAGC	78514
rs217837029	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77446904	CTGGGTGCTGAGTAC[C/G]TGTAATTTAACACCG	78514
rs217843983	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77264680	ACAGACACACACAGA[C/G]AGAGAGAGAGTCAGA	78514
rs217857247	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77448172	GTGCGCATGCGCGCG[C/T]GCACACACACACACA	78514
rs217857438	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77434931	GTGCTCCACCTGAGT[C/T]TCATCAACGCAGTGA	78514
rs217860948	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77324909	ACATGCAAAGTCTAT[A/G]CAGAAGGAATGCATG	78514
rs217866060	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77399976	GACCAGTTGAGACTA[C/T]AGATTCTGCCATTAC	78514
rs217877101	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77257598	GAAATGATGGGTTTC[C/T]GAAGCAAACTTTTCC	78514
rs217877196	snp	A/C/G			intron-variant	Arhgap10	GRCm38.p3	8:77481087	TCTACACATGAAATG[A/C/G]TGGCCCACTGTCCAC	78514
rs217887427	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77296938	AAAAGGATCACTGAA[A/G]GCACGAGCCCAACAT	78514
rs217887570	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77414510	CCTAGGGATGGGGGA[C/T]CAAGAAACATGGACT	78514
rs217910918	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77434357	AGACCCTCACAGTAG[A/G]AGCGAATTGACCCCC	78514
rs217915165	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77319462	AACAGGATTCTTGAA[A/T]AGTCTTGGGTTGTTT	78514
rs217934890	in-del	-/ACTGCTCTCGCAGAG			intron-variant	Arhgap10	Mm_Celera	8:77495605	GCAGCTACTAGGGAA[-/ACTGCTCTCGCAGAG]CAGACATCTACCCAG	78514
rs217952194	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77296132	GGAGGATGTAGAACT[C/T]TTAGCTCCTCTTCAC	78514
rs217963686	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77420750	CTTGGAGGTCGGCCT[A/G]TGTTAAAACAAGCAC	78514
rs217964077	in-del	-/TAAGGG			intron-variant	Arhgap10	Mm_Celera	8:77412020	AACCCTGAGCAAAGC[-/TAAGGG]TCAGAAGGAGGGAAA	78514
rs217966829	snp	A/C/T			intron-variant	Arhgap10	Mm_Celera	8:77440872	AGATGATGAAAAGAG[A/C/T]AGTGTACACAAACAC	78514
rs217972117	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77388592	TAAAAGAAAAATGAC[A/G]TGGGGATGAAGCAAG	78514
rs217973547	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77319815	AGAAACCATGTATTG[A/G]CAGGAACCAAGACTC	78514
rs217992079	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77421444	GCACAAAGGTCTGGA[A/G]ACTGGTGGGGAACGG	78514
rs217995241	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77251613	CTATCAATACATACT[C/T]GGCATAGTCGCATGA	78514
rs217997768	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77288775	TACGGTCTTTATGAC[A/G]CTTACGATGCGATGC	78514
rs218004483	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77289619	ATCCCTCTCACCTCT[C/T]TCTTAGTTACACGGC	78514
rs218016001	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77512733	CAATGCATGGCTCAC[A/G]CGGCACCACAAACAC	78514
rs218021303	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77289218	ATTAAATGTGAATGA[A/G]TCAATTATCTTTCTA	78514
rs218027620	snp	A/C/G			intron-variant	Arhgap10	GRCm38.p3	8:77288729	GCCGCCCATATGTTC[A/C/G]TCAGACTGAAATGGC	78514
rs218029783	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77507033	AAAGAGTTGCCTTTG[A/G]GGGATGGAGAGATGA	78514
rs218044245	in-del	-/AGAGAGATCT			downstream-variant-500B	Arhgap10	Mm_Celera	8:77250082	ATACTCAGTGGTATG[-/AGAGAGATCT]GCCCAAAGAAGCCAG	78514
rs218047641	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77330143	GTGCAGCACCAACAC[C/T]ATAGGCTCCTTATGA	78514
rs218051572	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77281419	CTGTTACAAGAAAGA[G/T]CATGGACACGAAACG	78514
rs218052582	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485606	ACTCACCTGAAGTAA[C/T]CTCCATTTCCACTTG	78514
rs218053612	in-del	-/AC			intron-variant	Arhgap10	GRCm38.p3	8:77253524	GGGCCTCTGCTTTCT[-/AC]ACAGAGTGTAAACTC	78514
rs218069772	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77476223	TCTCTTATATAGAGT[A/G]TGCTATCACTTCCAT	78514
rs218083738	in-del	-/ACTAGAC			intron-variant	Arhgap10	Mm_Celera	8:77253764	ATGTAGTGCACATGA[-/ACTAGAC]CTAGACACTAGACAG	78514
rs218086440	in-del	-/GCAATGGGAGCACG			intron-variant	Arhgap10	Mm_Celera	8:77415974	GATGCCAGGAGCACA[-/GCAATGGGAGCACG]GCAATGGGAGTGTGC	78514
rs218088507	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77370833	ACAGGTACATCTCCT[C/T]CTTCCCTCAGATGTC	78514
rs218094635	in-del	-/AAAAA			intron-variant	Arhgap10	Mm_Celera	8:77356172	ACTGTCTGTGATTAT[-/AAAAA]TAAAAAATGTACACA	78514
rs218103635	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77480336	CCATGAAGCTCTCTG[A/T]CCATCTTTGAACAGG	78514
rs218112261	in-del	-/TATACA			intron-variant	Arhgap10	Mm_Celera	8:77272218	TTTGTATAGCGTCGC[-/TATACA]AAACACTACCTGACC	78514
rs218115605	in-del	-/TTGGCTA			intron-variant	Arhgap10	GRCm38.p3	8:77255702	CTTGGGCCTCCTGGG[-/TTGGCTA]TTGGCTATCTTCTGG	78514
rs218125263	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77264151	GTAATTGAGCATCAG[A/G]TGAATGTTCTATCTC	78514
rs218125970	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77403407	GCTTGCACTGAACCA[A/G]ACAACTATATTAAAC	78514
rs218127590	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77282055	TCAGGCACTGCAGTC[G/T]GCAGAACTCAGTAAA	78514
rs218137944	snp	A/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493673	AAGCCTCCAAAACAC[A/T]GGCTGAAATGTTGGA	78514
rs218139309	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77268836	TCCCTTGGCCCTCCT[C/T]GGGATGGTGGCTCAC	78514
rs218148956	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77425689	GGAAGAAGGAAGAAG[-/AA]GAAGAAGAAGAAGAA	78514
rs218153298	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77324356	TGTTGTCACCTAAGG[A/G]CAAAACAGCCACATA	78514
rs218156017	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77267997	TCAGGGTTAGCAAAA[C/T]GAGGCAGGTGGCTGC	78514
rs218157403	snp	C/T			intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77492765	GTGTGACCATTTATA[C/T]CCTAGGAGTTCGAGC	78514
rs218160369	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77414281	AGCAGCCGCAGGCCA[C/T]GCAGTGAGTCACCAC	78514
rs218165128	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77355574	GCAGAATGCTTGGAT[G/T]TATGATCAAGTTATA	78514
rs218166877	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77399334	ATGAGAACCACTGGT[C/G]TACAGTGCCACTTCT	78514
rs218180858	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77262903	AGGCTCTTGGAGAAT[A/G]GGAAACGTTGATGAG	78514
rs218184197	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77341914	AAAAATAAAAAATAC[A/G]AACTTTGAAATACAC	78514
rs218200661	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77398190	TTTATTATATGTAAG[A/T]ACACTATAGCTGTTT	78514
rs218215938	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77420360	ACTGTAAATAGGTGG[G/T]CTGTACAGAAAATTA	78514
rs218222279	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77377230	AAGATGTTTTTTAAG[-/AA]AAAAAAAAGAATTAC	78514
rs218227821	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77398068	AGCTTTGCCCCTACA[A/G]AAGGAGGTAAATGGT	78514
rs218248764	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77348405	AACAACAGAGGCTGG[A/G]GTATAAGCAAGTTTA	78514
rs218251361	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77440206	CAAACTCAAAAGGGG[-/A]AAAAAATCAAAGAAA	78514
rs218255181	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77385182	TTTCCCTGGATGAAC[A/G]CATCAAATGCTAGGA	78514
rs218258925	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77506201	CGAAGGCCTTCTTTA[A/G]CACCTATAGATTACA	78514
rs218267343	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77471645	GCTCTCCAACTCCCC[-/T]TCCCCCCCCCCTTTT	78514
rs218270371	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77419506	TTATGGCACAGTTCG[A/C]CAATTGGCTTTGCAT	78514
rs218275314	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77404020	TGTGCATCTTAAATG[C/T]TTCCCTCTACCAAAG	78514
rs218278398	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77295580	TCAAATAAACTGAAT[A/G]TCGGGCCAAGAAGTG	78514
rs218279629	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77439433	ATCGATTTCAATCCT[A/T]AATTCCAATTACCTT	78514
rs218292971	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77288527	ACAAAGTCAGGAGAC[C/T]CCCTCACTGCTCATC	78514
rs218297211	in-del	-/GC			intron-variant	Arhgap10	Mm_Celera	8:77411501	TGCACGCACACACGT[-/GC]ACACACATACACATG	78514
rs218297965	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77356316	AAGGGAACAGATACC[-/T]TCCCCCGGCATCCAC	78514
rs218300069	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77356237	TAACTGCTCTTCCAG[A/C]AGACCCAGAATCCTT	78514
rs218312677	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77418408	ACTGTCACACAGGGC[C/T]TGTGACACAGGGTCT	78514
rs218314188	in-del	-/TTG			intron-variant	Arhgap10	Mm_Celera	8:77401600	AGAAATTTTGTTTTA[-/TTG]TTGTTTTTTTTTTAA	78514
rs218320679	in-del	-/TGGTTTTTTTTTTTGTTTGTT			intron-variant	Arhgap10	Mm_Celera	8:77368822	TCACAGAACTCTGCC[-/TGGTTTTTTTTTTTGTTTGTT]TGTTTTTTTTTTTTT	78514
rs218321887	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77369618	CTAAGTTAAAAATTG[C/T]CATTTCCACAGTGGT	78514
rs218336085	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77438948	ATAACTCAAAATCAC[G/T]AACCTAAATTCACTA	78514
rs218362667	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77368219	ATATGCCAAACTACA[A/G]GTGAGTTAGCACAAC	78514
rs218364512	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77374139	CCATACAACACTTCT[A/G]TAATCAATTCTTGAA	78514
rs218367337	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77461542	TCTCTGGTAACTGAC[A/T]AAGCCGTGCTGACTG	78514
rs218409893	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77379382	GATGTCACTTGGTGG[A/C]TCTGAACTATGTGCG	78514
rs218418212	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77368805	CAATTTTCTCATACC[A/G]TCTCACAGAACTCTG	78514
rs218420879	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77267684	ATGCCTCATCATCAA[A/G]CTGACTGTGACAACT	78514
rs218426705	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77348684	TCCTTGTGTATGTCC[C/T]AACCAGAAGGGGATG	78514
rs218432599	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77463118	GTCTACATGAGACTA[A/G]AGGTTTTGAAACTGT	78514
rs218443319	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77456791	GAAAGAACCCAGATG[C/G]CCCTCAACAGAGGAA	78514
rs218451345	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77268509	GATTTAGAATGTGCA[C/G]TTACAGCACAGCACA	78514
rs218472665	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77467442	GTCTACAGAGGTCTA[C/T]AGGTCTATAGGACAG	78514
rs218477033	in-del	-/TTT			intron-variant	Arhgap10	GRCm38.p3	8:77486353	GCCTGACAGCAACTC[-/TTT]TTTTTTTTTTTCTTT	78514
rs218477526	in-del	-/TGT			intron-variant	Arhgap10	Mm_Celera	8:77326978	TAATTTATTTCAAAG[-/TGT]TGTTAGGAATTTGTA	78514
rs218482140	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77340963	TCCCATGGAGCCCTT[C/G]GCATGCTCTCCATTT	78514
rs218487751	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77462860	AGCAAACCCCTTAAC[C/G]CATAGCAAGCAAGGC	78514
rs218488808	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77272908	TAGAAAGAGGAAGCA[C/T]AGACTAATGCCTTGG	78514
rs218501145	in-del	-/AG			intron-variant	Arhgap10	Mm_Celera	8:77427254	GCACCACCCGAAACT[-/AG]AGTCTGCTTTGCTTC	78514
rs218512661	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77347420	TTGTTGTTGTTTTTT[C/T]GAGGCAGGGTTTCTC	78514
rs218535173	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77412437	TCAAGACAGGGTTTC[C/T]CTGTGTAGCCCTGGC	78514
rs218535267	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77418496	ATGTGGCTCAGGCTG[C/T]TCTCAAAATCACTAC	78514
rs218538235	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77446049	CCAAAACAGGATTTA[C/T]TTTTTAATAATTAAT	78514
rs218540577	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77267405	AGGGTTACAGCTTTG[A/G]TCCAATCTTAGAGAA	78514
rs218541829	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77329391	TTGTTTATCCCTATC[C/T]TTTCTGTACAGGGCT	78514
rs218544049	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77273238	AATGACAAATCAGAT[G/T]TTCAAGAAAGAAGGG	78514
rs218551027	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77314987	GCTCCAGCAGCAGGT[-/A]TAATTATTTAGCACA	78514
rs218556545	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77485945	ACCAGAAAACACAGA[A/C]ATTTTCATTGGGATT	78514
rs218573624	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77340464	CCGGGGACTATTCTG[C/T]CTATTTGTAAATTTC	78514
rs218581705	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77504933	AGTGGCACAGTTCCT[C/T]CAACAAGGCCATGCC	78514
rs218585998	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77323360	CCCACTCATTTTGTA[C/T]ATCTGCCATAGACAC	78514
rs218588987	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77418133	AAAGGACGGGTGTTG[C/T]TGTCAGCCGTGCAAG	78514
rs218613116	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77323491	TTTATAACAAAATAT[A/G]TAAATCAAGAAAATC	78514
rs218631976	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77504628	AGGATCCATCATCAC[A/G]GGGCGAGCATGGCAC	78514
rs218638626	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77445133	AGGGAGTTGGTAGCC[A/G]ACTTCCAGACAGATG	78514
rs218639029	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77354536	AAAGAAAAGGGAAAA[C/T]CGAACACTGTAGCAG	78514
rs218639682	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77324736	CAACTACTGCTAATA[A/G]CTTAAACTGAAGAAA	78514
rs218642134	in-del	-/GGT			intron-variant	Arhgap10	Mm_Celera	8:77465863	TGGAGTGGGGGGGGG[-/GGT]GTCAGTAAAGAACTA	78514
rs218644825	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77472441	TCCAGAGGTCCTGAG[C/T]TTAATTCTCAGCAAC	78514
rs218671025	snp	C/T			utr-variant-5-prime, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77517845	GGCGGCAGCGAGCGG[C/T]TAGCAGGGCTGAGCG	78514
rs218678278	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77309772	GGGCATTCTGGGTCT[C/T]TCTGAATACACCCTC	78514
rs218697105	in-del	-/CGTCTTCC			intron-variant	Arhgap10	Mm_Celera	8:77471991	CCCAACAAGTGTCCG[-/CGTCTTCC]CATAAACACTGAGAG	78514
rs218705169	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77353860	TTCAACTTGCTACAA[C/T]GATTATTCTAAGTAT	78514
rs218714975	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77293802	GAGGGCTCATGAGTT[C/T]GTTGAGTTGGGAGGG	78514
rs218731187	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77294346	ATCTACATATGCTAG[G/T]GATATCACAGAATAC	78514
rs218743019	in-del	-/TTTA			intron-variant	Arhgap10	Mm_Celera	8:77508693	GTTTTGTTTTTTTTT[-/TTTA]AATATTTGGTGTGAA	78514
rs218747496	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77294619	CCAGATAAACATGCG[C/T]TCCCCCGAAGCACAG	78514
rs218758701	snp	A/G			downstream-variant-500B	Arhgap10	Mm_Celera	8:77250293	CTAACATCATGGTCT[A/G]CTGACCATGACTGTC	78514
rs218785764	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77287668	CATGCTCAAGCCGGG[C/T]GTGGTGGTGCACACC	78514
rs218812611	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77346660	AACACCTTTTCTAGT[A/G]AGCTTGTAGCTCACA	78514
rs218829519	in-del	-/TTTTT			intron-variant	Arhgap10	Mm_Celera	8:77363259	TGTGGCTTTTTTTTT[-/TTTTT]TTTTGGAAAGGAAGG	78514
rs218834952	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77412966	AAGTAAAATGCTGCT[A/G]GGTAGCACTGGTTTC	78514
rs218873838	in-del	-/TT			intron-variant	Arhgap10	Mm_Celera	8:77498820	GGTCAAGAGCTCTTC[-/TT]TTTTTTTTTTTTTAA	78514
rs218879207	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77378811	AGGAATGAAGGCTTG[G/T]GTAAAATGGCCCCAA	78514
rs218886252	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77424615	GGAGTCTGTCAGAAA[A/G]GCATACAAGCTTGAT	78514
rs218889742	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484276	CACACACGCTAAATA[C/T]ACACTTTATCACCAA	78514
rs218905910	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77272372	GCTTTAATGACCCCA[A/T]AGAAATTTTGATTTA	78514
rs218908498	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77266632	AGATATTAAACTATT[C/T]CAGAATAAAAGTTTA	78514
rs218909322	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77467715	ACACACACAAAGGCT[A/G]ATCTCTTCTAGGTAA	78514
rs218916890	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77437681	CTTATACCAAAAGGA[C/T]GTGAACCCTCAGATG	78514
rs218918271	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77327655	GGCTGAATCAGAGTG[G/T]AAGGCAAATTTGTAT	78514
rs218925387	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77504477	TTTTGTGATGGACAT[-/A]ACGGTGTAGACAGTA	78514
rs218930951	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77402489	ATAAAAAATCTTTTT[A/T]TAAAAAGTCATTTCT	78514
rs218942034	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77417985	GCAGAATAAAACTGA[A/G]GGATATTTATAAGGT	78514
rs218955184	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77266483	TGAAACAACTGTATG[C/T]TGTCACTGTTCTCAC	78514
rs218975318	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77321702	TTTTTTTTTAATGAC[G/T]GCTGTTGAGGCTGCC	78514
rs218998205	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77407180	CATAACAAAAATAAA[C/T]AGGGGCTGTAGAAAT	78514
rs219001546	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77490960	CAAAGCACAGGCTCT[C/T]CTGTGATTATCTGAA	78514
rs219025834	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77424152	GTTTGAGGCATAAAA[A/C]TCCTCTCTGAAGTAA	78514
rs219026601	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77294006	TCCTTCACTGACAAC[C/T]ACTTAGTGTTCTTCT	78514
rs219027850	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77443716	CCGGGCGTTGGTGGC[A/G]CACGCCTTTAATCCC	78514
rs219033367	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77322331	GGAAACCAGGAAGGA[G/T]CTTGGTCATGTCACA	78514
rs219066800	in-del	-/T			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519514	TGTGGAACTGTTGGG[-/T]GGGGGGGAGGGAGGG	78514
rs219078620	snp	A/C/G			intron-variant	Arhgap10	Mm_Celera	8:77271800	AGTTGAGGGAAAATG[A/C/G]CTTTATTGGGGGATG	78514
rs219083147	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77402711	AAAAAAGAAAAAGAG[C/T]GACTTTGTGTAGCAA	78514
rs219083614	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77516046	GCGTACAATGGCTCA[A/G]AAGCACACACACAGT	78514
rs219091418	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77292436	GAAAACACTTCAAAT[C/T]AGTCACTCTTGACAG	78514
rs219097393	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77510202	GGGGCTGGGAATTGA[A/G]CCTGTGTCCTCTGTG	78514
rs219097631	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77323380	GCCATAGACACAGAA[A/G]GAGGTTTCTGACCCA	78514
rs219099185	in-del	-/AC			intron-variant	Arhgap10	Mm_Celera	8:77261095	GAGAGAGAGAGAGAG[-/AC]AGACAGACAGACAGA	78514
rs219103171	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77402219	TGCAAAACTCAAGTT[G/T]AGGACTTGGAGGAGC	78514
rs219116007	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77441422	TTGACTTCCAACAAA[C/T]CCCACCACCAGAATA	78514
rs219151497	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77272172	AGCTGAGGATACAGC[A/G]TTTCTGTATAGCGCT	78514
rs219152276	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77354056	CTGCTTTCATGGGAG[A/T]ATAAAGACACCAAGC	78514
rs219160356	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77472846	CGGAGACAGGAGACT[C/T]TCCCAGGTCAAAGGC	78514
rs219165608	in-del	-/CA			intron-variant	Arhgap10	Mm_Celera	8:77439493	CAGTTCTAAAAACCT[-/CA]GTTTTAGATTTATTC	78514
rs219168322	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77309006	GTTAAGATATAATTT[C/T]ATTCCGAAGAATAGT	78514
rs219172346	in-del	-/CTAGACA			intron-variant	Arhgap10	Mm_Celera	8:77454986	ATGGAACTTACGAAG[-/CTAGACA]CTGGTGGAAGCTGAT	78514
rs219179356	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77483083	TAGGGATTCCTCCAT[C/G]CTCAGCAAGTCAGCA	78514
rs219201539	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77367084	TGGGTTCTAGGAATC[A/G]AACCTGGATCCTCTA	78514
rs219206612	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77421848	CTCGGTATGACTTGC[C/T]CTCACTCTGCTGAGC	78514
rs219217543	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77369360	CAGACCTATACTTTA[-/C]CCATGGGTTTCTCCT	78514
rs219223421	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77326737	TAGCTTCCCCCTTCC[A/G]GGTTAGATTTGCCAC	78514
rs219223704	snp	A/G			upstream-variant-2KB, downstream-variant-500B	Arhgap10, 0610038B21Rik	Mm_Celera	8:77518828	GTGCACACATGGCAT[A/G]CATTTTTCACAAACT	78514
rs219228853	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77416911	CTGAGACTAAGCAGC[A/G]CAGGTCTGTGAGCAA	78514
rs219229414	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77401754	CTGCATACATATATT[A/T]CCATGAAACAATATA	78514
rs219231689	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77422596	AGCATTAAAAACCAA[A/G]AAGGATGTAATCTTC	78514
rs219236784	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77464779	GGAGAGCTGGCTCAG[C/T]GGTTAAGAGCACTGA	78514
rs219246432	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77265274	AGTGCAATAATCTCT[C/T]GTAGTATGGGAAATA	78514
rs219249361	in-del	-/TAAA			intron-variant	Arhgap10	Mm_Celera	8:77480587	GCTCTTTTTTTTTTT[-/TAAA]AAAGATTTATCTTAC	78514
rs219249372	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77377384	TGTAAGCATATTTCA[C/T]GCTCTAAAATACTTC	78514
rs219254525	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77465234	AACAGGCAGACAGAG[C/T]GAACTGTTGTAAGTA	78514
rs219254973	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77345186	AGGCTAACATCACTG[C/T]GGACCTTGCCAGACT	78514
rs219275824	in-del	-/GAGT			intron-variant	Arhgap10	Mm_Celera	8:77422371	ACTCTCCATCCATAG[-/GAGT]TTTATAACAATACAA	78514
rs219277584	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77400663	GGTCCTCTGCAAGGG[A/G]AGTCAGTGCTCTTAA	78514
rs219279911	in-del	-/AAAA			intron-variant	Arhgap10	Mm_Celera	8:77381965	TCAGAATGTAACATT[-/AAAA]AAAAAGGGGGGGGCC	78514
rs219283763	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77357234	ATATATCTGCAAAAA[-/G]ACTCTTTTTAGTATC	78514
rs219285512	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77428108	GGCTCTCCATGAAGT[G/T]TGGCTCACTGGAAAA	78514
rs219287874	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77416312	ATGCTCCAGCTGCTA[C/T]GCCTGCCACCTCTGC	78514
rs219304501	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77471149	CAGAGACAAAATTTG[G/T]AGCTGTGACGAAAGG	78514
rs219312319	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77372677	ACCCAGCACAGACAG[A/G]CTCACACTGTCCCTC	78514
rs219313129	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77333111	CCTTTTAATTTTACA[A/T]TTTTTGTGTGTCTGT	78514
rs219324470	snp	A/C/T			intron-variant	Arhgap10	Mm_Celera	8:77509004	TAATATATATATACA[A/C/T]GTGTGTGTGTGTGTG	78514
rs219324901	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77428726	CAAAGATCTTCTAGA[C/T]TTCAAAACAATGTAC	78514
rs219329735	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77400977	ACAGCCAAGCCATTC[C/T]TGAAAGGAATAAAAG	78514
rs219330033	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77376832	CCCAAACACACCTAC[A/G]AAGTTTAATAATGAA	78514
rs219331616	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77299829	TGAACTCAGCCGGGC[A/G]TGGTGGAACACACCT	78514
rs219337872	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77442281	GAGGAAAAAGACAAA[A/G]TTACAAACAGCTGAA	78514
rs219357870	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77372264	GCCCTACCTGTCCCT[A/G]GATCTCAGCCGTAGC	78514
rs219358549	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77291711	TGTCGACAACAGCTG[C/T]CGGCTCTAAAAGAGC	78514
rs219358596	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77305888	TACTTGGCATCATCA[A/G]AAACCAGTATTCACA	78514
rs219361009	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77328005	GACTGTGGTCAGAAG[C/T]AGCAGTGGTATTTTT	78514
rs219361298	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77406694	GAGGAGTTTGCACTG[A/T]TGTGGAAGGAAAGGA	78514
rs219363909	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77373945	GTAATCTTTGGTGTC[C/G]GGGCCAAAGGCAAGA	78514
rs219366575	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77471756	TTAAAACACCTTTGG[C/T]CCAGCCCCCAACAAC	78514
rs219390366	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77516922	GAATACAGATGGAAC[C/T]GAGGTGGCCAGCTTC	78514
rs219392275	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77508502	ACTGATTGCACTATG[C/T]AGCTCTGGCTGGTCT	78514
rs219396662	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77441717	CCTTCCATCTTAGTC[A/G]CCAAAATCTGTTCCC	78514
rs219396663	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77447934	TAGCAGACCTCAAAG[C/T]CCGACTCTCCAGTGA	78514
rs219400384	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77516486	GGTGGATGAGAATGT[A/G]CACTCAGTACGTTTT	78514
rs219420636	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77370882	AAACACAAAGGATAT[G/T]AGAACTAAGAGGGGC	78514
rs219425665	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77327372	GAGCTGGGAGAATCG[C/G]GAGTTCAAAATCAGC	78514
rs219430750	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77271911	CACTGGCAATGAAGT[C/T]ACCTGTCTGTCACCT	78514
rs219434044	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77448236	ATGCTTTATTACCAG[C/T]CCACACCCCCATGTC	78514
rs219437601	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77487546	CCCTTCACCGCAGAC[-/A]GCCTCACCAGCCCCA	78514
rs219450465	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77490807	ATTATGATGAAACTC[C/T]GTTAAGTACTTGGGA	78514
rs219472245	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77371280	ATAACTCACAAGCTG[A/T]CCTGTGACTTACACA	78514
rs219479043	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77463912	CTCTCACACTGAGTT[G/T]GGAGATGAGTATATG	78514
rs219481023	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77270561	TGGCGATGCAAGACA[C/T]AAGATGTAGCCAAGA	78514
rs219497359	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77465423	CCACAGGCCTGAATC[G/T]ACCTTCCCCTACTGA	78514
rs219503866	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77271142	AAATGCCTCCGTGAG[A/C]TCCAGCTGTAATTTT	78514
rs219507027	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77325239	TCAGGAGGATAGCAC[-/A]AATTAGCTGAATCCC	78514
rs219507050	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77264867	AACAAACTGGCACTG[C/T]AGGCCCAACTGACCT	78514
rs219514540	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77449159	CCTGTGCACACTGCC[A/G]CATCCCTGGCCCTGT	78514
rs219524735	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77499911	GGGACACCCTACACA[C/T]AGACACCTTCCTGGC	78514
rs219526429	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77470047	GTTTGAACCAACTTA[A/G]CAAGTGTACAGTACC	78514
rs219535524	in-del	-/CATAGC			intron-variant	Arhgap10	Mm_Celera	8:77318359	GCTACATATATCAGG[-/CATAGC]CTTTGCTACATGCAT	78514
rs219545468	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77491354	TGGAAGCTGCAGTGG[A/G]TCCCAGTACATTTAC	78514
rs219546854	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77497340	TCAGCGATCTCCCCA[G/T]CCTCCTCAGAGAAGC	78514
rs219555016	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77464948	CTTTTTTTAAAAAAA[A/G]TGCCTTACCTAGAAA	78514
rs219567114	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77489675	TTTCCGAAGGCTGTG[C/G]TCTCAAAGCACTAAA	78514
rs219580599	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77376512	CTGGCAGCTCTCCAG[C/T]TCCCTCCCTCAGGCA	78514
rs219586597	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77414598	GAAAGAAAAAAGAAC[-/T]TTTTTATGCCCTTTA	78514
rs219589862	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77324327	CACACACTCTCTCTC[A/G]CTAACACTTCAAGTG	78514
rs219595818	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77292935	CATGAGGTGGCTTCT[C/T]GCCACAATTCAATTC	78514
rs219602709	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77305658	AACAGCCAGGTACAG[G/T]ATCCTTCCAGTTTCT	78514
rs219615777	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77385127	ATCCAATGACCGCCT[-/G]GGGGTAGAAGTTTAC	78514
rs219617379	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77253407	GGTGTGAAGTGCTAT[A/G]TCCCATGCTTTTGCT	78514
rs219619317	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77252572	TGGGAGAGCATAAAC[G/T]CAGGCTGAAGCCTTA	78514
rs219622255	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77489115	ACAGTCTCAGTGAGA[A/G]AGCCTGTCTCAATCT	78514
rs219635645	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77331906	CCGTGAAGTCAATAC[C/G]GAGCAGCGAGAAGTG	78514
rs219637119	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77498072	CGGAGAAAGCAAGAG[A/G]AACACCAGAACTGGA	78514
rs219639393	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77325612	GCCTACTCTGTACAC[A/C]ACAGTCCCTGATATT	78514
rs219645895	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77253392	CTCCAGCGCTGGAAT[A/G]GTGTGAAGTGCTATA	78514
rs219669446	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77297294	CTACGACAACTTTGA[G/T]ATGGGTGGAGTGGGG	78514
rs219679347	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77370646	GTTTCTGTTAGCTGT[A/G]GCTTTGCTTTCCAGG	78514
rs219688125	in-del	-/CTATGGGTCA			intron-variant	Arhgap10	Mm_Celera	8:77412825	CACAATGTGATGGAG[-/CTATGGGTCA]CTTCCCAACCACCAA	78514
rs219689754	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77326033	CAGAAAGTAACAGCA[C/T]GAGTCGTCCAAGCTC	78514
rs219695953	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77427212	TGCCCTCAGCTGCTT[C/T]GCTTAGCTCACTCAC	78514
rs219709314	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77375552	GTTAGCAAAGACACA[C/G]AAGATGACTGAGTCC	78514
rs219748498	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77426622	ATTCATTCCCCTTGC[A/G]GTGCTGTGCGCTCGT	78514
rs219749719	in-del	-/GAAGCCT			intron-variant	Arhgap10	Mm_Celera	8:77512016	CGTAATCATCTTCCA[-/GAAGCCT]GAAGAACTTCGAAAA	78514
rs219751549	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77513894	TAGAAAGCCCACAGT[C/T]GTCTAAACTGCTCTG	78514
rs219759256	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77356522	GCAGCACTCACACGA[C/T]ACCTATCTCTCCAGG	78514
rs219765598	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77446992	CTGCTTCTTCCAGCA[A/G]CTACCCCTCTTCTCA	78514
rs219772125	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77364991	CGGTACAAGAGAAGA[C/T]GTGTTCCTAAGTGCA	78514
rs219778466	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77451954	AAGTAAATTTGATGA[A/G]CTCCTATGACCCAGA	78514
rs219789617	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77421456	GGAGACTGGTGGGGA[A/C]CGGCTACACAGCCAG	78514
rs219796078	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77447715	TGCAGGCACTCTGAC[A/G]TGTGTCTTCGTGAGA	78514
rs219798077	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77290188	ATGAGGGAATCAGCT[A/G]TATTATAATCAAGTC	78514
rs219800664	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77297715	ACAAAGCACAGACAA[C/T]AGTGGTTTGGAAGGG	78514
rs219812076	in-del	-/ACACATTGAAG			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493383	CACTGGCCTACAGGA[-/ACACATTGAAG]ACACAACAGACTGCT	78514
rs219815953	in-del	-/TTGG			intron-variant	Arhgap10	Mm_Celera	8:77414761	ATTTGTATTTGTTTA[-/TTGG]TTTGTTTGTTTATTT	78514
rs219831055	in-del	-/CCCAAATAAGAG			intron-variant	Arhgap10	Mm_Celera	8:77416358	GCCAACTTTCAGGAA[-/CCCAAATAAGAG]CCCAAATAAGCTCTT	78514
rs219831810	snp	A/C/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77290785	AGGGGTCGAGACTCA[A/C/G/T]GGGTTGAGAAGCACA	78514
rs219844118	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77381587	GGTAGGTGTGGCTCC[A/G]GGAGAAGTTAGGAGT	78514
rs219848133	in-del	-/TGTT			intron-variant	Arhgap10	GRCm38.p3	8:77373535	ACCAGGCCAACTGTC[-/TGTT]TTCCTGTCAAGTGTC	78514
rs219860156	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77357554	GCCACGGCAGAGAAG[C/T]GCAGTTGTGATCGCT	78514
rs219872152	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494593	TGTTCTTGTTCCAGC[C/T]GCGAGTTTAAAACCT	78514
rs219872715	in-del	-/TAAAA			intron-variant	Arhgap10	Mm_Celera	8:77464940	AATAGATCTTTTTTT[-/TAAAA]AAAAAAAGTGCCTTA	78514
rs219874217	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77446514	TCAGGAGAGAATCAG[-/T]TCACTGCATGGGGGT	78514
rs219883836	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77269210	CTCTTTACCTCACTG[A/C]GCTGATATAAGCATT	78514
rs219896794	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77447157	CGTGTAGCTCTGGCT[A/G]TCTTAGAACTCTCTC	78514
rs219907690	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77313779	GGTATGGAGCTAAGA[A/G]TATTGATAAGGGCAC	78514
rs219912568	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77419439	TCTGGTTGTTAGTGT[C/T]GCACTCACAGGCCAA	78514
rs219926071	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77331547	AAACTGAGGGGGGAG[A/G]AATCTAGATGGGTCA	78514
rs219928867	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77421457	GAGACTGGTGGGGAA[C/T]GGCTACACAGCCAGG	78514
rs219932351	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77300126	AGAAAGAAGAAGAAG[A/G]AAGATGAAGAAGAAA	78514
rs219932957	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77469680	CCAGGGGATATGGAA[C/T]CCTCTTCCGGCCCCC	78514
rs219937360	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77487430	GTGTGCACACATGTG[C/T]ACATACCCACGGAGG	78514
rs219949163	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77269845	TAAAATACTACAGTA[C/T]CAACTAGGAACACTT	78514
rs219955162	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77488212	CTAGTATCACTGCCC[C/T]TGGGGACCAGAACAA	78514
rs219955626	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77330164	CTCCTTATGAAGTCT[G/T]CCTGTTACCCTCCCT	78514
rs219955992	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77409266	CCACGCTCTCCTTCA[C/T]TACTCTCTTCCTGAT	78514
rs219988419	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77351279	TCCAACCTCCTGTAA[C/G]CCGAACGCTGGCCTG	78514
rs219990545	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494457	GTCCTAGTTTATAAT[A/G]CAAAACATGTGGGCG	78514
rs219997866	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77324279	CGAACAAAGCAGCCA[A/C]CAAGCTTCACAGTAA	78514
rs220004268	in-del	-/ACCCAGCT			intron-variant	Arhgap10	Mm_Celera	8:77410334	CCTAAGCAAAATGTC[-/ACCCAGCT]ACCCAGCAAGCAACA	78514
rs220029165	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77399198	TATCCTGCATAGCAG[A/C]TATTTACATTACAAT	78514
rs220037160	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77446928	AACACCGTATTCTTG[C/T]TCTGGGGTGCCTGTG	78514
rs220037988	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77452531	CACACTGGGCCAGAC[A/G]TGGTGGCGCATGCCT	78514
rs220038417	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77324804	TGTCTACTTCTATAC[C/T]GGCATTACTATACAC	78514
rs220050103	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77513938	GTTATTCTACAGAGT[G/T]CGGAGGAACGACAAA	78514
rs220065231	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77297735	GTTTGGAAGGGTTTT[C/G]TCTCACAATGCTTTA	78514
rs220066634	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77475730	ACATACAAACAAATA[C/T]ATACAGTGCAACACA	78514
rs220074763	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77297192	AAACTCAAATTTGAA[C/T]ATACCTTTTTAATTG	78514
rs220087206	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77252650	TTTCTTATGCCTTTC[C/T]CATCTCAGGGCAGGG	78514
rs220091665	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77295693	CCTAATAAAAATATT[A/T]AAAAAATTAAACTGA	78514
rs220094673	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77399829	AATGTGGCTTCAAGG[A/T]ATGTCATAGGAGAGG	78514
rs220109270	in-del	-/TT			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485809	GTGGCCTGTGAACAG[-/TT]TTGGGAAAAGCAGGT	78514
rs220121026	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77273425	CTGGACCATTAAAAA[A/G]AACACAACAAAACAA	78514
rs220130826	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77312912	ACGGCAAAAATCAGA[A/G]CACCAAAAAATATTT	78514
rs220140856	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77374495	ATAGAGCAGGCTGCC[G/T]ATAGCCTTAGAAATA	78514
rs220147291	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77513421	CTGCTATAAAAAGGG[A/G]AAACGAACACTCCAG	78514
rs220148644	in-del	-/AATT			intron-variant	Arhgap10	Mm_Celera	8:77370155	GGGACTCGGGAGTGA[-/AATT]ATAGAGCACGGTACA	78514
rs220154858	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77370114	CTGAGGGGGGGGGGG[-/G]CGGGGGAATAGGAAA	78514
rs220156877	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77468512	CTGATGGCCAATTAG[C/T]TGGGCAGGAAGTGGA	78514
rs220160559	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77274257	GGAGAAGGAGAGAGA[A/G]AGCTTTCATTCACTA	78514
rs220161332	snp	C/T			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519487	TTCTCTGTTTGAATG[C/T]TAGGTCCCTAGTGTG	78514
rs220162859	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77415879	ATCAGCACTGCAAAT[-/A]AAATAATAAATTAAA	78514
rs220178697	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77470768	AAGATTTGTATGTTA[C/T]ATATGTTATATTGTG	78514
rs220181718	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77289745	AAGCGTAGCCACACA[-/C]GGCTTGGTGACAGCA	78514
rs220185392	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77380550	TTTTATCTAAAATAA[G/T]ATTACTATAAAATAT	78514
rs220187707	in-del	-/TT			intron-variant	Arhgap10	Mm_Celera	8:77514655	GAGCAGTATGTGCTC[-/TT]AAGTGCTGACCTGGC	78514
rs220206463	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77273722	CTGTTATAGACACGC[C/T]GAAATACCTACTGCA	78514
rs220206769	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77514610	AACCACCTAATATGG[C/G]TGCTAGGAATCCAAC	78514
rs220212921	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77432214	GGCTCCCCTGTGGCA[C/T]AGCTGTTTGCTGTAT	78514
rs220223126	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77329752	CTTCCAGGGGACCCA[A/C]ATTTGATTCCAGCCC	78514
rs220225882	in-del	-/CCCGC			upstream-variant-2KB, nc-transcript-variant	Arhgap10, 0610038B21Rik	GRCm38.p3	8:77517993	CCCGCCTCGGGCGCG[-/CCCGC]CCCGCCCCGCCCCCG	78514
rs220237015	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77335887	ACAAGTCCTACTCTG[A/C]TGGAGAATATGTCTG	78514
rs220241021	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77474496	GTCATTTCTGTGTCA[C/T]ACGTACACACATTGT	78514
rs220241826	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77269015	GGGTCTTAATAATCT[A/T]GGTGGTAAAGGGCTG	78514
rs220250255	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77267572	CCAATAGGGTCCCTG[A/C]CGAGACTGCTTCCAC	78514
rs220279364	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77403063	CCTCATGCTTCAGGA[A/C]CACAGGGCACTATGC	78514
rs220280493	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77408352	ATTCATCTGTGTCGA[C/T]GATTTAAGCAGAAGC	78514
rs220286253	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77425872	AAAACAGGCCTAGCT[G/T]AGTCTACTGTGTGGG	78514
rs220287565	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77418731	AAAGTCTAGAACAGC[A/G]GTTCTCAGCCTATAG	78514
rs220290426	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77404340	GCACTATCGGAAACA[C/G]GGGAGCAAGGATCCT	78514
rs220292536	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77280139	CAGGGAAACAGCTGT[-/G]GGTGAGAAGCAGGTT	78514
rs220298063	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77269940	GAGAGTTTCTTGGAA[C/T]GTGCCAGGTAAATGG	78514
rs220302918	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77348575	AAAGGTACTACGGTT[C/T]TCCTGTGGTCCTCAC	78514
rs220303568	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77330255	AGGGAAGGCGGTGAA[C/T]ATAGAAAGAATGGGG	78514
rs220307577	in-del	-/TCT			intron-variant	Arhgap10	Mm_Celera	8:77420930	GGACATACAGAAAAG[-/TCT]TCTTCCCAAACTCTA	78514
rs220318438	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77473840	GTAATCAGTTCGGAT[A/T]CTTATGAAGTACATG	78514
rs220325447	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77512634	ATCTACAACACCAAT[C/T]CCAACAAAATGAACA	78514
rs220333180	snp	G/T			synonymous-codon	Arhgap10	GRCm38.p3	8:77409634	CAAAAAGAAAGCCTC[G/T]CCATCCCCCTGCAAA	78514
rs220338286	in-del	-/AT			intron-variant	Arhgap10	Mm_Celera	8:77403009	GCTGCACACACACAC[-/AT]AAAGACCTGCGTTGC	78514
rs220338825	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77273798	AACAAAACAGGAAGA[A/G]CCCACTTACCTTAAT	78514
rs220340260	snp	A/C/G			intron-variant	Arhgap10	GRCm38.p3	8:77310189	CCTGGTTGGACGGGA[A/C/G]AACCACCACCTGCCC	78514
rs220341599	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77424954	GGTGTGTGAGTGTGT[G/T]TGTGTTCTCAACGAT	78514
rs220351029	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77251383	CGCTGGAGGCCTCTG[C/T]GCATGCAGCACTTTA	78514
rs220352032	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77374645	ATGTTACTCTTGGTG[G/T]TGCTCTTGGTAACTG	78514
rs220374075	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77294770	TTCAACAAAATGTGC[C/T]GCAGTTAACACGTTT	78514
rs220374960	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77311274	ATCTTTTCTTCCAAC[A/T]ACACAAACAGAAACA	78514
rs220383919	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77473149	ATACCAACAGTGGTC[A/G]ACAAGAAACGGCTCA	78514
rs220398464	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77379767	GGTCTGTCACACACC[A/G]AGGTTCTCCTAATCT	78514
rs220404264	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77311365	CTCGGTTCTTATTTA[C/T]ATTCTTCATAATTTC	78514
rs220405761	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77445392	CAAATGCCAATATGT[C/T]CCCCCAAAACTGTTT	78514
rs220409097	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77512062	AAGAGCCAGCTGTGG[A/T]GGAGCACACCTTGTG	78514
rs220424414	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77278918	ACTGACTGGACAGAG[A/G]TGTCTGGGGAGACAT	78514
rs220426194	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77405000	CTGAGACACAAAGGT[C/G]CTGCCTGATGGGCCC	78514
rs220432226	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77500673	ATGGCAGGGACTCAC[A/G]TGTCAGGGAGGTCCA	78514
rs220435590	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77372919	GGCTCCTGTGAGAAA[A/C]CCATGAGGACAAGTC	78514
rs220435948	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77378924	GAAGGGAGGGGCTAC[A/C]GCGAAGCACAGGGTA	78514
rs220442602	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77467392	GACTCAGGAGGCAGA[A/G]GCAGATGGATTTTTG	78514
rs220454471	in-del	-/G			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519406	CTCACAAACAAAGCT[-/G]GGGGGTGGGGGTGGG	78514
rs220463301	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77374195	ATTTAAATCACTATC[A/G]CCCCCTGTATAAATC	78514
rs220466785	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77450534	CCTTGACCAAGAACT[C/G]ATCACATAACCACCA	78514
rs220473892	in-del	-/CT			intron-variant	Arhgap10	Mm_Celera	8:77444137	TAGTCCAAACCCCAA[-/CT]CTGATTTGCCAGGAT	78514
rs220474855	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77444508	GAAAAAGTTATGCAC[C/T]TCGAAACCCTGTCCT	78514
rs220493198	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77373398	CTCATCTCAAACCTC[A/G]GCCTGGGCTAACGCA	78514
rs220498767	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77466750	CTACAAATTTGCCTA[A/C]AGGCCAATCCAATGG	78514
rs220500188	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77272594	CAGAGGCTCTTCTCT[A/G]GATAATACATATGGT	78514
rs220511415	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77295748	AAGTTGTTTTCAATT[A/G]CTTTTTATTACCTAG	78514
rs220532398	in-del	-/CCC			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77503970	CGGAACCCTCATGAG[-/CCC]CCCCCCCCCCCTCCA	78514
rs220537874	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77272946	CAGTAAGTGGTTCTC[A/C]TCTTTCTCCAGAAGG	78514
rs220538584	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77251404	CAGCACTTTACTTGC[A/G]ACCTAGAATGCCCTT	78514
rs220559481	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77465923	CAGGGGCCAAAAACA[C/T]ACTGATCTTGCAGAG	78514
rs220559659	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77472542	GTGTACTCATTCATT[A/C]ATTAAATAAATAAAT	78514
rs220564042	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77380911	AAGTCTACCATTAGC[A/C]CGACTGTGCAGACTG	78514
rs220578183	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77354983	CCTAGGCAGAGGCTG[A/G]GAGCCAGGCCTCTCT	78514
rs220586664	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77468420	AACCCTGTTGGAGTA[C/G]ACAGGGCGGTGTGAA	78514
rs220587651	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77407938	TCTGCTTTAGTTCTT[C/T]GTCTGTTTTAAAGTT	78514
rs220594519	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77431293	TAAAGATTTAACAAC[A/G]TAATGTAAGGGATGG	78514
rs220598052	in-del	-/CATAT			intron-variant	Arhgap10	Mm_Celera	8:77472149	ATATATATACACACA[-/CATAT]ATATATATATACACA	78514
rs220599258	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77354148	GCTATAAAAGGTATA[C/T]ACTACCTCAATGTTT	78514
rs220618571	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77336572	ACTCTTAATCCAATC[C/T]CCAATGTGAGGTACA	78514
rs220627243	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77272987	GACAGAAATCAGACT[G/T]AATAGCATAAGAGAT	78514
rs220628676	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77474017	CTAGATGGACAGCCC[C/T]GCCCCCCAACCTGGC	78514
rs220629028	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77254737	ATGCCTGTTCTTGCT[A/T]GAAGATTCCAAGCTA	78514
rs220632291	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77347599	GAAACTCTGAAGAAG[C/T]AGTCATAGGCTCCAC	78514
rs220633624	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77383382	TAAATGTTTGCTTAT[A/G]ACCAAGCTGGCATAT	78514
rs220640698	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77474302	AGAAGCATCCAACAC[A/G]GATCAGAGAAGCATC	78514
rs220640939	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77467884	AGCTGTGGACACGTG[A/G]GATGAATGGGGAATG	78514
rs220642303	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77421843	GTGTCCTCGGTATGA[C/T]TTGCCCTCACTCTGC	78514
rs220658451	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77374975	TGCATGGGATCACTC[A/C]TAAGAGGAATGCAGA	78514
rs220661122	snp	C/T			intron-variant, missense	Arhgap10	GRCm38.p3	8:77491977	TGTTCATCATAGAGT[C/T]GTCCACTGCCACGGG	78514
rs220678907	in-del	-/CCCTGCCGCGG			intron-variant	Arhgap10	Mm_Celera	8:77438169	TCACCTGCCGCCATT[-/CCCTGCCGCGG]CCCACACCTTGCAAG	78514
rs220684313	in-del	-/TG			intron-variant	Arhgap10	Mm_Celera	8:77400526	ATGTGAGTGTTTGCC[-/TG]TGTGTGTATGCAGTA	78514
rs220694132	in-del	-/CG			intron-variant	Arhgap10	Mm_Celera	8:77285238	AAAATCCAATATATA[-/CG]CGTGTGCGTGCGTGC	78514
rs220714385	snp	A/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77491645	AGCTCACCCAATGCC[A/G/T]CAGCAGGCAAGGGGT	78514
rs220717097	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77330833	TTCTTTATGTGAACA[C/T]ATACAGAACTGTTCT	78514
rs220718996	in-del	-/TC			intron-variant	Arhgap10	Mm_Celera	8:77308613	AAGAGGTTTTTTTTT[-/TC]CCTACTTTTATCATG	78514
rs220727662	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77334435	GCGCGGAGAGAGAGA[A/G]AAGGAGGCAGTTTCA	78514
rs220727822	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77328307	CGGTTTGTCCTTCCA[G/T]TTGTTTCCCTGACAA	78514
rs220728021	snp	A/G			downstream-variant-500B	Arhgap10	Mm_Celera	8:77249994	CATGTTGGCATGGCT[A/G]TCAGCCTACCCATCC	78514
rs220731916	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77423726	CTGAGTAGAAGCTAT[C/T]TGAGCCAGTATCTGA	78514
rs220743987	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77378510	GTGGTTTTACATCAC[C/T]ACACAGTCCATGTGT	78514
rs220769049	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77424230	TAGACCAAAAAGTCA[A/G]CAGCTGCCCTTGCCG	78514
rs220771136	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77498426	CTGAAGGTACCAGCA[A/C]ACACACAGAAATACA	78514
rs220779723	in-del	-/AGA			intron-variant	Arhgap10	Mm_Celera	8:77351686	TCCTGGAAAAAAAAA[-/AGA]AAAAAAAAAAAACAC	78514
rs220785161	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77404216	CACTGCACAGGGACA[G/T]CTGGACACACAGATG	78514
rs220787023	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77328757	CTCCTTCCATGCCGC[C/T]CCATGTATGATGTCC	78514
rs220787670	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77359553	GCTAGTTCTAAGACA[A/G]CCAGCTGTACTCAAG	78514
rs220804413	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77454227	CCCAGCGCTTCACTG[C/T]TGGCGGGTGGCGGCA	78514
rs220805957	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77448034	GATTCTATGGGAGCC[A/G]TACATACTCAAGCCA	78514
rs220808134	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77362179	GGGGAACAGAATGGA[A/G]AAATGTTCTTATCTA	78514
rs220822841	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77356348	GACAGTGCACACACA[G/T]GGCACACAGGCATCC	78514
rs220824950	in-del	-/ATATATATAT			intron-variant	Arhgap10	GRCm38.p3	8:77472129	TGATTTTATATATAC[-/ATATATATAT]ATATATATATATACA	78514
rs220833669	in-del	-/GTCTTTAATTTTAACTTCTTTGG			intron-variant	Arhgap10	Mm_Celera	8:77463758	TACCAGGTGAATAGT[-/GTCTTTAATTTTAACTTCTTTGG]GTCTTTAAAGAGTTT	78514
rs220844717	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77403564	ACTGTGTTTGGTTTT[C/T]GCTTGTCTTGAGGTT	78514
rs220844774	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77430305	TGGCTGGTCAGCTGT[A/C]TAAGAAAGCAATTTT	78514
rs220847241	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77360191	ATGCCTCAGCTAGAA[A/C]CAAAAAACTAGCTGT	78514
rs220848374	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77429165	GGGAACAAGGACCCA[A/G]TGCAAGCAGCTATCA	78514
rs220855732	snp	C/T			utr-variant-5-prime, nc-transcript-variant	Arhgap10, 0610038B21Rik	GRCm38.p3	8:77517887	CAGCACGGTCATGTC[C/T]AGCCCAGCCCAGCGA	78514
rs220864628	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77453822	CTTCCTGCAGGAGGT[A/G]TTTACTCTCTGTTCA	78514
rs220872144	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77500009	AGAACGCAGCTCTAC[A/G]GTTGATGTGTGTCGA	78514
rs220876189	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77311955	GGGTTTAGCTGAACA[C/T]CCTAGAAATGTCACC	78514
rs220881879	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77499539	ATCTTGTCTCCGGCC[C/T]CTCAGCTTCCTTTAC	78514
rs220887669	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77426544	AATAAAGCAAGGGGC[A/G]CGAATCATGGCGGAG	78514
rs220899755	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77487238	TTCCCCATTTCAGCA[-/T]TATGAAAGATCCCCA	78514
rs220904450	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77384194	GTCCTCACTGCCCGA[A/T]GCCCGCCCTGCACAG	78514
rs220906733	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77353769	TCAAAGATTTACACA[C/G]AGCCATTTAAGCAGT	78514
rs220909414	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77309020	TTATTCCGAAGAATA[A/G]TAGAATGTGGATCTA	78514
rs220911459	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77255627	ATGAGTATACACATA[C/T]TTTATGACTCTTTAA	78514
rs220913858	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77469585	GGGCTGGAAGGGTAT[C/T]TCAGCAGTTAAGCGC	78514
rs220922786	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77296276	GAGAGATGGCTCAGT[A/G]GTTAAGAGCACTGAC	78514
rs220944809	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77293909	GTTTCCTCTTGTTTG[A/T]GAGTTTGGGGACTAC	78514
rs220957842	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77449890	AGCAACAGACAGGCA[C/T]GAGTAACCACGTTAG	78514
rs220969773	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77457636	ACCCAATAATAATAA[C/T]AATAATAATAATAAC	78514
rs220976166	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77472108	AAAAATAATCGTTTG[C/T]TAAAGATGATTTTAT	78514
rs220984768	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77378966	GAACTAGGCAGATGC[C/T]CCTCAACTCCCCTGG	78514
rs220985463	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77513325	TCATGAGTCACCTGA[A/C]CAAAACCAGGACCGA	78514
rs220998443	in-del	-/TGCA			intron-variant	Arhgap10	Mm_Celera	8:77380623	TTTCTCTGATCTTGG[-/TGCA]TGCAGGTGGGATATG	78514
rs221005569	in-del	-/TG			intron-variant	Arhgap10	Mm_Celera	8:77366443	GTCCTCTTATCCATT[-/TG]TGTGTGTGTGTGTGT	78514
rs221017293	snp	C/T			intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77493013	TATACATTTTTAACC[C/T]CAGCACTTGGAAGGC	78514
rs221017526	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77334510	ACACCGGTAAAGACA[A/G]AGTGAGCAGATTAGA	78514
rs221023111	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77431921	GAGAGGGGAGAGGAG[-/T]GGGAGGGGAGGGGAG	78514
rs221024963	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77455552	ACAAAGAATGCATGC[A/G]CTCTCAGTGTGCGGC	78514
rs221032590	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77459023	CATTCCCTCCTCCTC[-/T]TTTATTTGCTCACCA	78514
rs221033288	in-del	-/TCTC			intron-variant	Arhgap10	Mm_Celera	8:77363241	AATATTAAGCATCTT[-/TCTC]TGTGGCTTTTTTTTT	78514
rs221036384	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77333979	CAACATCCTGGGAAA[C/T]CATCCCCATAAAAGA	78514
rs221041052	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77424226	GCAGTAGACCAAAAA[G/T]TCAACAGCTGCCCTT	78514
rs221043086	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77376223	AAGAGTTCTTAACTG[-/AA]AAAAAAAAAGGGGGC	78514
rs221046143	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77272092	CCCAGGTCAGAACCA[C/T]AGCTGCTGTGGGTGC	78514
rs221054248	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77490886	AGAGCCCACAGCAAC[A/T]CACATGCTCTTTATT	78514
rs221062329	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77455927	CCCCAAATTGTTTTA[G/T]CCATAGTGTTTCACC	78514
rs221066228	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77329543	GTATGCACACCTGTG[G/T]GCAATCACATTGACT	78514
rs221068882	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77408060	TGAGGCTAGGTTCAG[A/G]ACCTAGCCTTTATCA	78514
rs221073132	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77279408	GCTGAGAGGGACTTG[A/G]CTGGTGTGGTGCTGC	78514
rs221088594	in-del	-/ACACA			intron-variant	Arhgap10	Mm_Celera	8:77405994	ACAATACCCCCCCTC[-/ACACA]CCCACAGTGCACTGA	78514
rs221104354	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77499564	CTTTACACCATGACA[C/T]GAAACAGCATCCACA	78514
rs221106609	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77490111	AAACATACTGAGCTG[A/G]GAGTCAGCAGACAGT	78514
rs221108408	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77448356	ATAACATTATACAAA[C/T]ACTAGTTGAACCTGT	78514
rs221112516	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77327534	GTCTTTCACACGACT[C/T]ACCTAGCTTCATTCA	78514
rs221116565	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77361597	ATAAAAACCACCTAG[A/T]CTTTTGTAAACTAAG	78514
rs221126126	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77316000	CACCTCTTCGGGATA[G/T]ATTCTGCAAGTGCCA	78514
rs221127188	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77273329	GGCTATGAGCAAACA[C/T]ACAGAGATCTATCTA	78514
rs221137613	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77401633	AAATACTTAGTGTTT[C/T]TAAAAAGAAACTTAA	78514
rs221152440	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77360918	TTATTTTGAGATTCA[C/T]ATTCTTTCTATGGAA	78514
rs221153073	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77497132	AGTGTGATTTTTTTT[A/T]TATTTATTTAATGTA	78514
rs221166923	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77317303	GCTCTGGTTCCAGAA[A/G]ACAAATCCGGAAGTA	78514
rs221170194	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77308417	TTTAGTATAGAATTC[C/T]ATCAGATCTTCAAAG	78514
rs221174852	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77434376	GAATTGACCCCCTCG[A/C]CCAGGTTCTTATCTG	78514
rs221175512	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77449782	TCTTGGGCAGACCAT[G/T]TGGATCAGTTTCTCC	78514
rs221176569	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77298727	GGAAGAAGTCAAAAT[A/G]TCACTGTTTGCAGAT	78514
rs221179401	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77316650	AATATTATGAACCAA[A/G]TGCCAGTTACGATGC	78514
rs221200495	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77260740	CAGCTTGGGGCGGGA[A/G]GGGTTTGTTACCAAG	78514
rs221216425	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77275848	GTTCCATGCCGCATG[A/G]TGTCACTGTCCTGCA	78514
rs221225485	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77354194	TAAAATATGCATTGA[G/T]ATTCATGAAGAAAAT	78514
rs221238382	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77498985	TGCCTCGCCCCCTGC[-/T]CCCTGCCCCCTGCCC	78514
rs221238809	snp	A/C			intron-variant, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77517293	TTGCGGGAGACTGGA[A/C]GCAGCGTTAGGGCGC	78514
rs221245054	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77376643	CCCACTCTCAACCTC[G/T]CACCCATGCTGATTA	78514
rs221248047	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77423852	TTACTCTGAGCAGGT[A/G]TGCAATGCATGGCAC	78514
rs221248485	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77454981	AAGCCATGGAACTTA[C/T]GAAGCTAGACACTGG	78514
rs221248929	in-del	-/CCCCCCCCCA			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	GRCm38.p3	8:77515761	AAACTAGCCCCCCCC[-/CCCCCCCCCA]CACACACACACACAC	78514
rs221264457	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77309062	ATGCCTGAATCTGAT[C/G]ACCTCCACTAGCAAA	78514
rs221275557	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77339659	GGACAAGAAGCACCA[A/G]CTAGCTGCTCAGCCC	78514
rs221285516	in-del	-/TC			intron-variant	Arhgap10	Mm_Celera	8:77412740	CCAGCTAAGCAGCTT[-/TC]CCCAGGCCACAGCAG	78514
rs221290252	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77358918	GCGTGCACGGGGCTT[-/G]TCTCCACTGGCACTA	78514
rs221308714	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77332080	AGAGGATGATGACAG[C/T]ATCCGAGATGAAGGA	78514
rs221311600	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77378529	CAGTCCATGTGTGCT[A/G]TGCTACTTCACCATA	78514
rs221336366	snp	C/G			utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250629	TCCCCCTGAAAACCC[C/G]ACAGCGGGTGTGTGG	78514
rs221340849	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77334023	AGAGCTGGGGAAGTA[C/G]CAGAAAAGTGGTGGG	78514
rs221349902	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77410589	TTCACAGGGAGTGAC[C/T]TTATGAAAACTCTGC	78514
rs221351938	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77486052	GAACTGTATTAAAGA[A/G]TAGCATCAGGAAGGC	78514
rs221365263	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77279041	AAGCAGAGAAAGTGG[G/T]GCACACTAGACTGAG	78514
rs221378785	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77472960	GCACATGTGCACATG[C/T]TCACATCTGTTTTCA	78514
rs221386724	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77313819	GGCCAGAGATCATAT[C/T]GCCCAGCAACTGTGC	78514
rs221387001	snp	C/G			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77515717	CACAAGTCACAAATT[C/G]CAGAAGGTCTACCTT	78514
rs221397144	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77405413	GATGCACACAGAAAT[A/G]TGGTGCCCACAGAGG	78514
rs221401510	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77427932	GTGGTAAAGTTATAT[A/G]GATCTTAGGAAGCAA	78514
rs221401903	snp	A/G			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519309	TCCTCGATCCCATAA[A/G]CTGAGGCAAGAGGAT	78514
rs221407704	in-del	-/GGGAGA			intron-variant	Arhgap10	GRCm38.p3	8:77509573	TTAAAAAAAGGGGGG[-/GGGAGA]GGATAAAGAATTTTG	78514
rs221424555	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77297943	GCCTTATTAGGAGGT[A/G]TGGCCTCGTTGGAGT	78514
rs221428235	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77432130	TGGTGGGGGGGGGGG[G/T]GGAAATTATTTCCCT	78514
rs221430655	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77406205	AGACCCACCCCTAAA[A/T]GAAGGAAAAAGTATA	78514
rs221444738	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77514681	CTGGCTCTCGCTCCA[C/G]CCGCTCCACAGTTTA	78514
rs221449502	in-del	-/AAGATGACGTC			intron-variant	Arhgap10	Mm_Celera	8:77383762	GGAAGACTGAAGATA[-/AAGATGACGTC]AAGTAAAGAGAGAGA	78514
rs221455603	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77258029	CCTCCCTTGAGGAAA[C/T]GCCTCCATGAGATCT	78514
rs221455918	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77368860	CTGTTCTTGTTTTTA[-/T]TTTTTTAACATAACT	78514
rs221459103	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77476311	CATAACAATGCTACA[C/T]TCCAAATCTAAGATA	78514
rs221459179	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77252699	ACACTGCAGCTGCTC[A/G]GGCAGACAGAAAGAG	78514
rs221462323	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77369294	GTTCCCTTTCAACTT[-/A]AAAAAAATCTAAACC	78514
rs221471675	in-del	-/GC			intron-variant	Arhgap10	Mm_Celera	8:77489304	CGCGCGTGCACATGA[-/GC]GTGCATGTGTGAGTG	78514
rs221478733	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77282107	GAGACTCGCAGTTCC[A/C]CTAAAACTGAGATAG	78514
rs221484123	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77453359	TAATAATTAATAATC[-/A]AATGTGATTGCTTTC	78514
rs221491426	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77253104	ATACAGAGACTAGAA[C/G]CCCTGCCTCCCCTCC	78514
rs221503750	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77283423	TACTTTTCTTATAAA[A/G]CTAACCGAGGATTTC	78514
rs221505715	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77274399	TCCTCTTCTCCTCCA[A/G]TCAGGTAAGGGCCTC	78514
rs221518057	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77475812	AGATAACTACTGGAG[C/T]TCTCGGGCAAATTCT	78514
rs221522699	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77411753	CCACACATGCTCCAG[C/T]CCAGGTGCTCAGCCA	78514
rs221537117	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77382033	CGTGTGTACATAAGC[G/T]CAAGCGTGCGCGCGC	78514
rs221539906	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77409325	TGCTCCAAGTTTCTC[C/T]TCCAGGTGACAGCAC	78514
rs221555366	snp	C/T			intron-variant, utr-variant-5-prime	Arhgap10	GRCm38.p3	8:77492126	AATGACTAGGTCCCA[C/T]GTGCCCACCTTGCTC	78514
rs221566669	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77274960	AGATGGCCTAGTCAG[C/T]CATCAGTGGAAAGAG	78514
rs221574191	in-del	-/GA			intron-variant	Arhgap10	Mm_Celera	8:77282657	GACAGGCCCAGGAGC[-/GA]TTTGAGCATCTGCTT	78514
rs221584286	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77409716	CAGGTTCTGCGCTCG[C/T]TTGTAAGGAGCCAGA	78514
rs221598946	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77255865	ACATTTGACCCAGTT[A/T]TGACCAAAGGCATGT	78514
rs221601893	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77407285	CAACCATCTACAACT[C/T]CAGTTTCTGAGGATC	78514
rs221605729	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77382476	TCTGTGGTATTTTCT[A/G]TGATGATAGGGCTAC	78514
rs221606291	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77499826	CCCTCACCAGATGAG[A/G]GACTGTATTAAAGAC	78514
rs221619852	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77260144	AGTTCACAGTCTCCT[A/T]AGTGTGAGGGGCAGC	78514
rs221620126	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77385934	GTTAGTACCACGGTA[A/G]TTCTGCTCCTTGAAC	78514
rs221623103	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77256516	GAAACAATTTGCTTG[C/T]TATATAACAACCCTC	78514
rs221627741	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77251858	TTTTATACTAGAAAT[A/T]CATACACCCCTGGTG	78514
rs221629096	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77308464	GCTCTTCAAACCATT[C/G]CTCAAAATAGAAACA	78514
rs221629414	in-del	-/CGTCTT			intron-variant	Arhgap10	Mm_Celera	8:77509346	ATGGTACAGGATTAA[-/CGTCTT]CCTCAGGAAACACAG	78514
rs221633972	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77297101	TACACAGTAAGCCTA[-/G]GGGGAAGACCTGCAT	78514
rs221639592	in-del	-/AAAA			intron-variant	Arhgap10	Mm_Celera	8:77274729	AGGAGAGTGGGCATT[-/AAAA]AAAAAATGTTTCTTA	78514
rs221657763	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77386391	CCAAGTGCCAGGATT[A/C]AAGAAATGTTCAGGG	78514
rs221658634	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77380638	GTGCAGGTGGGATAT[A/G]AATTAAAAAGCAGTA	78514
rs221675727	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77501110	ACTGCAAGACACACG[C/T]AGCAAACTACAGCAC	78514
rs221676304	snp	A/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494624	ACAAACAGATGAACC[A/T]GGTCCCTCCGCAGCT	78514
rs221683199	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77252169	ACAGACTCACACTGC[A/G]GTTATCGGCTTTGCC	78514
rs221686616	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77281512	GCTAGAAGTTGCTCC[A/G]TCTGATGCATCCCTT	78514
rs221699850	in-del	-/GTATGTGTGTGTGT			intron-variant	Arhgap10	Mm_Celera	8:77443963	AGCAGAACTCAGAAA[-/GTATGTGTGTGTGT]GTGTGTGTGTGTGTG	78514
rs221701837	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77380961	AGTTAATGTCAGTAA[A/G]TTTCTAGCCCCACCT	78514
rs221702934	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77501950	GCAGATCTTCAAGAG[A/G]ACTTGGTGGTCTCCC	78514
rs221718095	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77500741	GCAGATTCAGGTCAC[C/G]AGGCTGAAGCAGCAA	78514
rs221723005	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77357670	TCCAGCCCTATGCTC[C/T]TTTCTGTGATAAACA	78514
rs221726462	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77471343	CAGTCAGCTATTGGA[G/T]GGGTCACACGACCCC	78514
rs221729809	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77364907	GCATTCTTCTGTCCT[A/C]CTGCTTATTAAGTCC	78514
rs221730076	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77362203	TTATCTATTTTAATC[G/T]TAAACAGCAAAGGGG	78514
rs221734415	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77448372	ACTAGTTGAACCTGT[C/T]AGTGCATGCTGGGAA	78514
rs221741541	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77450636	CTCAGCTCCACAGCC[C/T]AGACTGTCCCCTCAT	78514
rs221756144	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77383780	GTAAAGAGAGAGAAA[-/C]GCACAGCTGAGAAGC	78514
rs221756400	in-del	-/AAA			intron-variant	Arhgap10	Mm_Celera	8:77376222	AAGAGTTCTTAACTG[-/AAA]AAAAAAAAAAAGGGG	78514
rs221767516	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77355865	AGAGGTCACTGTTTA[C/G]TCTCGAGTTTTCCAT	78514
rs221772474	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77362618	GCATTTGGCAGGTTC[A/G]TGCCCTGCCTCCTTT	78514
rs221778105	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77262951	GAAGAGAAGCTGCAA[A/C]GCTATCCGCTCAGAA	78514
rs221780912	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77456052	GCACCTAGAAGCTTG[C/T]ACTCCATGGCATAAA	78514
rs221781687	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77383220	GGACAAAAGGTTTAA[A/G]AAAGGTTTTTGTTAA	78514
rs221785119	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77257711	TTGTGGGATACACAA[A/G]GCATGTTTACTTGTG	78514
rs221797365	snp	A/C			intron-variant, downstream-variant-500B	Arhgap10	Mm_Celera	8:77358511	AAAATGACTCCTGCC[A/C]CTTCTGTCAGGCGGG	78514
rs221810142	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77356368	CACAGGCATCCATGA[A/G]GTAAAACATCCAGAC	78514
rs221821714	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77476406	TTCATACATTAAGAT[C/G]ATCTCTGGACACATG	78514
rs221825950	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77470812	ACCTAAGTGTATTTC[A/G]TTATACCACGTGCAT	78514
rs221827284	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77499018	GCCCGCTGCCCGCTG[-/C]CCTCTGCCTCTGCCT	78514
rs221847361	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77480974	CAAAGCCATGATGAT[G/T]CCTAAACTGAGCATT	78514
rs221848540	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77474508	TCATACGTACACACA[G/T]TGTGTCACAAAATAT	78514
rs221855739	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77377916	TAGCTCATCTCTTCT[C/T]CACAAACCAGGCGCA	78514
rs221856272	in-del	-/TC			intron-variant	Arhgap10	Mm_Celera	8:77348057	CTGTCTTTTCCTGTG[-/TC]TGCTTTTTTAGCTTT	78514
rs221858215	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77498424	CCTGAAGGTACCAGC[-/AA]ACACACACAGAAATA	78514
rs221890794	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77289589	CCAAGGTTCTTCCAG[-/C]CCCTCCCAACCCCAA	78514
rs221937002	in-del	-/CAT			intron-variant	Arhgap10	Mm_Celera	8:77378702	AGGAGAATGCTAAGC[-/CAT]CATCTCTCTCAGAAA	78514
rs221937684	in-del	-/ACAAGA			intron-variant	Arhgap10	Mm_Celera	8:77371434	AAAGTAACACTACAG[-/ACAAGA]GCTGGGGAGATGGTT	78514
rs221952572	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77330884	CCTTCCCCATAACCT[A/G]CTAATGCAACCATTT	78514
rs221955515	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77336960	TTTATCAGCTAAGGA[A/G]CAGGCTTTAAAGAAC	78514
rs221957146	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77426565	CATGGCGGAGCTTCT[A/G]AGACAGCGCCACTCT	78514
rs221961309	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77406070	GTTACTCGGCCAGGC[A/G]GTGGTGGCCACACCT	78514
rs221977623	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77267219	AGGGGAAAGAGCACA[-/G]AAAGCATCCATGCCT	78514
rs221983173	in-del	-/GAA			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493255	GAGAAGAAGGAAGAG[-/GAA]GAGGAGGAGGAGGAG	78514
rs221988018	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77429703	AAAGCAGGGTCCCTG[A/G]CAAGGTTGAGTGTGT	78514
rs221990391	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77310158	CTGTGAGCTGAAAGC[C/T]AGCTGGCAGGGATAG	78514
rs221995197	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77425237	CTATTATAAATAACT[-/AA]GTTATTAGTCAAGCC	78514
rs221999003	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77411346	CACACACGTGCACAC[A/G]CATGCACACACACGC	78514
rs221999283	in-del	-/TCTGCCTA			intron-variant, downstream-variant-500B	Arhgap10	Mm_Celera	8:77358298	ATACCTGCCTGCATG[-/TCTGCCTA]CTACCGTGCTTCTCA	78514
rs222004631	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77252600	TTACAGCTCACTGAG[A/G]CTCATCTCTGATGCC	78514
rs222007430	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77437225	TGCCTTATTCTGATC[A/C]ACAGCAGCTGTTTGA	78514
rs222015546	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77331417	CAACATGCACCGCCC[C/T]GCTACCCTTCTGAGG	78514
rs222019930	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77426082	GTGCCACTGTGCCCT[A/G]TATGAGTAGCTGTAT	78514
rs222020071	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77433324	CTGCTGGCAGGCAAC[C/G]AATGGGGTGCAGGGG	78514
rs222025239	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77315304	ACACCACAAGTAAAA[C/G]TGAAAACTAGTTTCC	78514
rs222040069	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77502729	CACATGCAGCTGTCA[A/G]TGCTGAAGAACTGCT	78514
rs222043342	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77366630	ACATAGCACTGTGGC[C/T]ACAGTGCACACTGCC	78514
rs222052831	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77428812	AGAAGAGATCACTCA[C/T]TCAGTTCATGGCCAT	78514
rs222076717	in-del	-/CCC			intron-variant	Arhgap10	Mm_Celera	8:77378864	AGGACGAGTGAGCTA[-/CCC]CCCCCCCCCCATGGG	78514
rs222077429	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77432408	TGGGAGGAGTGTCCA[C/T]AACATTAAGGCTGGC	78514
rs222078079	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77258710	GACTCAACCAGCCAC[C/T]GATTCAAAGTATTAA	78514
rs222080646	snp	A/G			upstream-variant-2KB, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77518138	TCCGAGGCAGCGGCG[A/G]TGGAGAACGTAGTCT	78514
rs222081009	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77340505	CTCAGAACTGAGTTC[C/T]CCCACGGTCCAATGA	78514
rs222084254	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77406910	GTCCGTAGGCAGCAG[C/T]AATACAACAACAACA	78514
rs222090804	in-del	-/GGTCCAGCGGCAGCCTGT			intron-variant	Arhgap10	Mm_Celera	8:77435483	GTCCACATGCTGAAG[-/GGTCCAGCGGCAGCCTGT]GGTCCACTGGCAGCC	78514
rs222098027	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77471920	TAAAAGGGCATTTAC[A/G]AACTGAGAGTCAAAT	78514
rs222111851	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77331932	AAGTGGATGACTTTT[-/C]CTGGCATGCTTACGA	78514
rs222116476	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77312595	GAAGATGGGATGTCC[A/G]GATAAGGCTATCGGG	78514
rs222116495	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77294420	CATTTAGCAGACCAC[-/T]TTTCTCGTCTTCTCT	78514
rs222124664	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77452561	TGTATCCCCAGACGT[G/T]GTGGCGCATGCCTGT	78514
rs222125704	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77253519	AGTGTTGGGCCTCTG[C/T]TTTCTACAGAGTGTA	78514
rs222133743	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77334657	ACCAGCTACCCAGAG[C/T]TCAGAAAGAACTAGA	78514
rs222135697	snp	A/C/G			intron-variant	Arhgap10	GRCm38.p3	8:77340889	TAGCCCGCAGTGAGC[A/C/G]CACGCATGCATGCAC	78514
rs222150176	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77414969	AGGTCTGGTTTTCCT[C/T]CATGTCACCACCTGC	78514
rs222154500	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77316109	ACTGCCACCCATCAG[A/T]AGAAGATCCTTCCTC	78514
rs222162521	in-del	-/AATGAC			intron-variant	Arhgap10	Mm_Celera	8:77456647	AAAGGAATGATGGGA[-/AATGAC]AAGCTGATAAAGTAC	78514
rs222176004	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77452249	GCAGAGATGATGGAC[A/G]GATTTGTCTTCTATT	78514
rs222180160	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77458497	CAGTTCTGGGTGTTA[C/T]TATGCACACACAACC	78514
rs222182735	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77310111	CCACGAATCACCAAT[-/C]GACTTTTGTGGGGCT	78514
rs222192460	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77407431	ATAGATAGATAGAGA[G/T]GGATGGATAGATAAT	78514
rs222194181	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77431049	CAAAAGAACACAAGC[A/G]TGTGGTTGTCAAAAC	78514
rs222203898	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77335965	TTTGAATATAATAAA[C/T]TCTCTCTCTCTCTTT	78514
rs222217480	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77409777	CTGTGCCATTATCAG[C/T]GTGACCACTACTAGC	78514
rs222218863	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77449596	TTTTAGAAAACATGG[C/T]TGTTTACTTTGAAAA	78514
rs222225028	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77312930	CAAAAAATATTTCAG[-/AA]AAAAAAAAATGGCAC	78514
rs222231561	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77457838	CAGCACCTGACCACT[G/T]GTTCTTTTGTTTAAA	78514
rs222235979	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77292002	AATCTTGGTTTTTTT[-/A]AAAAGAAGATAATAA	78514
rs222241129	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77288605	AGGGCACACAGGAAA[A/G]AGCAGTTCCCAGCAG	78514
rs222248825	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77430427	CACTGCCCAGAAAAA[A/G]GAAACGGCGTGAAAA	78514
rs222249249	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77471400	AAGGAGCTAAAGGGA[A/T]CTGCAACCCTATAGG	78514
rs222251058	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77316690	ACGTACTCCTAGCTA[C/T]ACAAAGGGAGCCCCT	78514
rs222259959	in-del	-/GAGAACTA			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77502662	AACAGGCTAAACACT[-/GAGAACTA]AAAAATGACCAAGTG	78514
rs222265001	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77336595	GAGGTACAGACAACC[G/T]AATATCTACCTTGGA	78514
rs222266550	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77382575	TGGAAAGCGTCGAGG[A/G]ACTCCCGCCATCATT	78514
rs222272149	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77435720	GTTCTACCTGAGCTC[A/G]GGCAAGCCAAAGCAC	78514
rs222276747	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77273707	AAACTGACCTTATAC[A/C]TGTTATAGACACGCT	78514
rs222282585	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77506949	TCCTACCATGCTCTG[C/T]CGCCACAGGTCCAAA	78514
rs222282703	in-del	-/GGGTGT			intron-variant	Arhgap10	GRCm38.p3	8:77412286	AACAGTCTGTGTGGG[-/GGGTGT]GTGTGTGTGTGTGTG	78514
rs222284133	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77338340	CAATGCAAATGCTAC[C/T]TAAAAGGTTGTTACT	78514
rs222284520	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77413471	CCCGACTCTTCAGAT[C/G]GAAGGCATCCAACAC	78514
rs222285448	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77319939	CAGGCTCAGGTATTA[A/T]GGAGCAAGGCAAATG	78514
rs222286485	in-del	-/TGTGTGTGTGTGTGTG			intron-variant	Arhgap10	GRCm38.p3	8:77445955	ATAAAATATAAAGGC[-/TGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT	78514
rs222289964	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77285345	CTAACACAAGAATTC[A/G]AAATAGTGCTGAGAT	78514
rs222321099	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77317152	AAATCGGTCCTGGAC[G/T]CAGTACAGAAGATGT	78514
rs222327163	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77318160	CTTGGTCTTGTCAGG[C/G]TATTTTAGTACAACA	78514
rs222340948	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77499902	GGAGGGAGAGGGACA[C/T]CCTACACATAGACAC	78514
rs222349215	in-del	-/GAACA			intron-variant	Arhgap10	Mm_Celera	8:77381858	AGCAATAAGGCACTT[-/GAACA]AAATGTGCTAAGAAT	78514
rs222361160	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77413024	CTTTTAAGATTTTTA[C/T]TATGTGTCTAGGTGT	78514
rs222362252	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77252721	CAGAAAGAGCTGGCC[A/G]AAGGCAGCTGTACTT	78514
rs222365642	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77276982	ACACCCGTCCCCTTC[C/T]AGCCAGGAAACAGAA	78514
rs222405037	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77278141	AGTTCCCACATGCCC[A/G]TGAACACCGAAGGGA	78514
rs222417327	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77342768	CTCAATGGAAGTGTG[A/G]CAGGACCATAAATGA	78514
rs222422799	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77318562	GCTAAATACCAGCCT[C/T]TTCTCCGGTGTGAGC	78514
rs222439066	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77314704	CAGGCTCCTCAGATG[G/T]AGTGAGGCAGACGCT	78514
rs222443032	in-del	-/TGT			intron-variant	Arhgap10	GRCm38.p3	8:77257738	TGTGAGCACTTGAGC[-/TGT]TGTGCATTTGCAAAG	78514
rs222447536	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77411435	ATACACATGTACACA[C/T]GTGTACACATGCACA	78514
rs222454839	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77258077	TCAATTAGTGATCAA[A/G]GAGGGAGGGCCTAGC	78514
rs222465507	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77381035	CAGTGTGCTTTTACA[A/G]TGTGGCCCCTGGTGG	78514
rs222478079	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77278822	TACTGACTCCTGACC[C/T]GACTCAGAGCTAAGG	78514
rs222480603	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77312087	AAATTGCTGTGGATA[A/C]GCATTTGCTAATGAA	78514
rs222491761	in-del	-/TGTGCTGGACA			intron-variant	Arhgap10	Mm_Celera	8:77324991	CCAATGCACTGTAAT[-/TGTGCTGGACA]GCATGGGTTTGTGAA	78514
rs222498088	in-del	-/CA			intron-variant	Arhgap10	Mm_Celera	8:77267036	GAGTGCCTGGGTAGG[-/CA]CTCTGAATCTGACCT	78514
rs222499036	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77341567	CCACGCCTCCTGTCC[-/G]AGTGCTCTGTACTCA	78514
rs222501007	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77499836	ATGAGGGACTGTATT[-/A]AAGACTCACAGCATT	78514
rs222501227	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77411826	TGTATGTGCTACAAC[A/G]CCCAAGAGCTCCTCA	78514
rs222519235	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77258734	GTATTAAAAACAAGT[C/T]ATCTGGATGGTGCAG	78514
rs222524522	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77379636	CCCAGCTACATTCCG[C/T]CTACATCTTAGCTGA	78514
rs222527128	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77279589	CTTCTCCTGCAGATA[A/C]GTTTGTGTGTTTGAA	78514
rs222540874	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77382167	CCTTATTTAAAAAAA[-/G]AGAGAGAGAAATTCT	78514
rs222541319	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77282500	CCCCACAAAGGGCTG[C/G]GCCCTCCCTGCTGTC	78514
rs222546627	in-del	-/CAAGCCAGCTAGAAC			intron-variant	Arhgap10	Mm_Celera	8:77339349	AAATAAGACATTCAA[-/CAAGCCAGCTAGAAC]CTGGATTATAGTCCT	78514
rs222548629	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77395798	CAATTAATACATAAT[C/G]ACAGCACACTGACTG	78514
rs222554043	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77498380	ATTCCAGTATACTCC[G/T]GTGGTTTAGACTGAA	78514
rs222556894	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77319019	AGGAACTGAGCAGAC[-/A]AGAGTTATGTAGAGT	78514
rs222565122	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77280655	TCAGACTGGGTGAGA[C/T]TGGATCTCTCACGGG	78514
rs222571389	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77398597	AAGTCTTCATTTTGT[-/G]TTTTTAAAAGACTGT	78514
rs222575544	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77395693	CTCTCAGTCAGAACA[C/T]GCATCACCAATCTTC	78514
rs222584478	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77460564	TGACACAGACCTTGC[A/G]GGAGCAAAGGCACAG	78514
rs222585637	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77428244	CATGTGTCATCTCTT[C/T]TCATTTTCATCAAAC	78514
rs222594066	in-del	-/TC			intron-variant	Arhgap10	Mm_Celera	8:77327682	TATGTGCATTTTTTT[-/TC]CTCCCTCAGAAGGAT	78514
rs222604362	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77275075	GGGTGGGGGAGGGTG[G/T]GGGGGACTTTTGGGA	78514
rs222604835	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77401764	ATATTTCCATGAAAC[-/AA]TATAATTCTACAAAC	78514
rs222620841	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77382710	ATAAAGCTGCGGGCA[A/G]AGCATGACCGTTACC	78514
rs222620900	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77396277	AAAGACATTGGAAGG[A/C]AGGCAGAGAGCAGCA	78514
rs222622958	snp	G/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503865	GAGTTTAAATGGAGG[G/T]CCTCACAGCAGTGCG	78514
rs222641256	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77417008	CAGCTGTCTGCTCCC[A/G]GTGGAGGAAGTCATT	78514
rs222642461	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77452597	CAGACGTGGTGGCAC[A/G]TGCCTGTATCCCCAG	78514
rs222663951	in-del	-/TTTT			intron-variant	Arhgap10	Mm_Celera	8:77328041	TGATGTTTAGGTGTG[-/TTTT]TTTTTTTCTTTTTAA	78514
rs222664138	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77285528	TTCAACATTTTATCA[A/C]GGGAAGCAACAGAGC	78514
rs222665804	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77273372	TAAGTGTGCAGGAGA[C/T]ACACGCAGGTCCTTG	78514
rs222682154	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77383252	TGCTGGGCAATAAGC[C/T]TAAGTTAAAATTTTG	78514
rs222690520	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503324	TTGTCCTTCTGAAAC[A/G]TTTGTGTTTCTCAAG	78514
rs222691532	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77408537	AGGTGTGGTGAGGAT[C/T]AAGGCAGATAACGCT	78514
rs222705446	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77479142	CCACTGAGTAAAAAA[C/T]TCTGGAGGTTTCCAG	78514
rs222712559	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77261749	TAAATTCTTTACAAG[A/G]AAATGAATCTCTAAT	78514
rs222714053	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77254351	AGCACTGACTACTCT[A/G]CCAGAGGTCCTGAGT	78514
rs222715346	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77357236	TATATCTGCAAAAAA[-/C]TCTTTTTAGTATCAA	78514
rs222721599	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77312261	CGAATGGGGAGCAGA[A/C]GAGTTGGGTGGAGAG	78514
rs222737383	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77371751	CCAATTTGTGCCATC[G/T]TTGTATATGTGGTGT	78514
rs222751359	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77254687	ATAAACTGGTTTGTC[C/T]TTGCCTACATTATAA	78514
rs222751903	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77256021	ACCAGTGAAAGACTC[A/G]AGTCACCAGCTGAGA	78514
rs222755763	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77459742	CCTCGGGCAAGCCTC[A/T]CTGAAATGCTCTCAC	78514
rs222768856	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77478539	TGGGTCTAAACTTTA[A/C]TCTCTCAATTTGCCT	78514
rs222771121	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77320441	GTCCTCACCAAAGGC[C/T]AGCGATATTGGGCTT	78514
rs222782117	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77434267	TCCAATCCACAGACA[A/C]TCTCCATAAATGAAG	78514
rs222793138	in-del	-/AC/CC			intron-variant	Arhgap10	Mm_Celera	8:77469359	ACACACACACACACA[-/AC/CC]CCTCGCATGCTGGAC	78514
rs222803081	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77365700	AGCTTCATGTGTTGA[A/G]CATGTGTAGAACAAA	78514
rs222811559	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77265314	AGTCCTGAACAGCTG[C/T]CCCATCCAAGTGTTT	78514
rs222814283	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77384309	TGTGGCCAAGGATGG[C/T]TATTTTAAACTATAT	78514
rs222820449	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77459126	GCCTCTCTAGAGTAG[C/T]ACTAAATATAGGCTT	78514
rs222825330	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77387935	GTGGTACCTGCTCTG[A/G]CAGCTGACTTGGAAT	78514
rs222841350	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77379200	CGGGTTTCACTGCCT[-/A]AAAGCAGACACCAAC	78514
rs222849585	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77258158	CTAAGGGAAGCAAGG[C/T]AGTAAGCAGCATTCC	78514
rs222849628	in-del	-/ACTT			intron-variant	Arhgap10	GRCm38.p3	8:77444172	AGAAACTGAATCCTC[-/ACTT]ACAGGCTGGCAAGAA	78514
rs222851097	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77265705	GAGCAATCTGCCCAG[A/G]TCTATCACAGGGACA	78514
rs222854715	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77343496	ACAACAGTCACCTAA[C/G]AGAAGACTTTAATCC	78514
rs222878204	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77384885	CAAACTGTCATTTTT[G/T]TAAATTTAGCATTAG	78514
rs222884766	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77452956	AATAAGTCATTTTTT[A/T]AAAAAGTGTTCCTTT	78514
rs222886514	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77381488	GATGAGACACTAACC[C/T]GCACAGTCCCACACG	78514
rs222904972	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77386475	GAGTTCAAATGCCAG[A/C]AACCACATGGTGGCT	78514
rs222912754	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77337100	TACTCACGGACGGAC[A/G]GACGGCCTTTGGGTT	78514
rs222915548	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77415415	CAGAGGCAGTCACAT[A/T]CACTCGTGCATACAG	78514
rs222927312	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77483828	TCTGCTTCTTGGCTG[C/T]TGCCAGCCACAAGAG	78514
rs222934739	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77367184	TAAAAGATGCACAAA[C/T]TTCAAATACATGGCT	78514
rs222935341	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77344410	ACTGTGCTCAATCAC[A/T]CCTGCACTGTGTACT	78514
rs222946752	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77283569	TGGGTCCCCAAAACT[G/T]CAGGAGAACATATAA	78514
rs222964942	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77370121	GGGGGGGGCGGGGGA[-/G]ATAGGAAAGAGGGGT	78514
rs222969828	in-del	-/CCCT			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503979	TCATGAGCCCCCCCC[-/CCCT]CCAGCAACTGTTAAA	78514
rs222971935	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77501876	GCACCAAATGCTGGT[G/T]AGGTCTTAGCCTGGC	78514
rs222973170	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77504663	GCCAGCATGGTCACA[C/G]AGCAAGAATGGCACA	78514
rs222979539	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77373538	AGGCCAACTGTCTGT[C/T]TTCCTGTCAAGTGTC	78514
rs222990174	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77363109	ACTTCTCTGAAAAAG[A/G]AAAAAAGACAGTTTT	78514
rs222996631	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77433333	GGCAACGAATGGGGT[A/G]CAGGGGGAGGCCAAG	78514
rs222999055	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77473607	GCTTATATGCTGCAC[A/G]CAGATGAAAACCAGA	78514
rs223003431	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77483371	GAGGGAGAGAGAGAG[A/T]GAAAAGGAGGAGAAG	78514
rs223005464	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77337626	CTCCGAAACTCCAGA[C/T]ACTTCTGCAGAGAAT	78514
rs223007167	in-del	-/ACA			intron-variant	Arhgap10	GRCm38.p3	8:77406914	GTAGGCAGCAGTAAT[-/ACA]ACAACAACAACAACA	78514
rs223037154	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77346476	TTTGTTTAGGAGCTG[-/AA]AAAAAAATAATGAAT	78514
rs223043515	in-del	-/GTGTGT			intron-variant	Arhgap10	Mm_Celera	8:77348007	TGTGTGTCTGCCTTC[-/GTGTGT]GTGTGTGTGTGTGTG	78514
rs223044653	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77369574	ATTTTCCCGGACATG[A/C]ATGCTCACTAGTGCA	78514
rs223044798	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77260810	TGCCACAGCTAACTC[A/C]CCTTGCTTTTTTATA	78514
rs223056716	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77361449	TATGCTTTATCACCT[C/T]GGATCGTTTCCAGTT	78514
rs223058551	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77473030	AGTGTCCACACTGAC[A/G]GCATTAGCTCAGGAG	78514
rs223071606	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77440331	ACCACCTGGGCTGAA[A/G]GGCTCATGCTAATGT	78514
rs223082776	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77408845	CTAACTCCATTCTTG[G/T]CCAGATCACATAAAG	78514
rs223095128	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77371377	TTCACCTGTAATATG[C/T]CCAACGTTTTCTGTC	78514
rs223097291	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77467064	AGCAGGACTAAAGGC[-/A]GAATGTTCACAAGCC	78514
rs223099970	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77312769	ACAGGCACTACTGGG[C/T]TTACACCAGAATATG	78514
rs223106243	in-del	-/CTCAGGTGA			intron-variant	Arhgap10	Mm_Celera	8:77347082	GACAAGTGAGCTGTC[-/CTCAGGTGA]CTATAATATGGGCCA	78514
rs223111079	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77500415	CATCCTACCTGAAAA[A/G]GGAGGATACAAAGTA	78514
rs223111335	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77453732	GGCCATGTGGCATAG[A/G]GCCTAAAGCATGCTG	78514
rs223114564	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77481032	CTACCCGCACTGACC[A/G]TCTACACATGAAATG	78514
rs223119855	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77362776	TTCAGAATGAAAGGA[A/G]AACCGTAAGAGAACT	78514
rs223122248	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77256572	ACATGCACTGTGGCG[A/T]TATGTTCCACAGAAG	78514
rs223136948	in-del	-/AAA			intron-variant	Arhgap10	Mm_Celera	8:77287914	GGGAAAGAGAAAGAG[-/AAA]AAAAAGGGAAAGAGA	78514
rs223143602	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77342130	CATATGGAGACTGTC[A/G]CAGAACGCGACAACT	78514
rs223166305	in-del	-/TGACCT			intron-variant	Arhgap10	GRCm38.p3	8:77252406	TCTTCATCCCCACAG[-/TGACCT]TGACCCTGACCTTGT	78514
rs223167097	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77428902	ATGAACATAACTGTA[C/T]ATTGCACCAGAATTT	78514
rs223183843	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77432588	TTTTCACTTTCCCTC[A/C]CTGAGTGGGAAAAGT	78514
rs223200457	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77281324	TGAGGGTGGAAACCA[C/T]GTCTCAGGCTTGGTA	78514
rs223204975	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77260833	TTTTTATACAGCCCA[-/G]GACCACTTGCCCAGT	78514
rs223214191	in-del	-/TGTT			intron-variant	Arhgap10	GRCm38.p3	8:77436534	ATGGCAACGTTAGTG[-/TGTT]AGTTAGTAACTACTG	78514
rs223215653	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77384972	TTCCTACACCTGGAA[C/T]TTTCAGATAGAAAGG	78514
rs223216108	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77475595	ATGCAAACCAAACAC[A/G]CACAGGCATAAAATA	78514
rs223218002	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77438660	GCGCCCTTTCTGAGA[C/T]GATCAGAAGGCCACT	78514
rs223225355	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77342833	GTAAGACTCACTGCC[C/T]CAAACAAACTGTCTT	78514
rs223232041	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77436289	AGAGATGGCCGTGGA[C/G]GTGTCTCCATGGCAG	78514
rs223237859	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77340918	ACGCACATGCATGCG[C/T]GTACACACACACCAA	78514
rs223248992	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77440741	TGGCCTGTATGGGTA[G/T]CCATGCAAGTATGGC	78514
rs223251484	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77439718	AAGTTGGCTAAAAGG[A/G]AGAGGAACAAAGCAA	78514
rs223269598	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77288505	TTGCTCCCTTCCTGG[C/T]TGTACAACAAAGTCA	78514
rs223272633	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77366743	TTCTTCCTGGCAATA[C/T]TGAGATGAATTAAAC	78514
rs223277007	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77438557	TAAAAGAATTGAATC[-/A]AAAAAAATTCTGCCA	78514
rs223285592	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77481441	TGATGGCTTTGCCTC[A/G]TGGATGTCATACACA	78514
rs223286753	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77336732	GGACGTGAGGCAGGC[A/G]GTGAAAACCAGGGCG	78514
rs223293063	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77435836	TCATTGCTGTGAGGG[A/G]ACACTATGACCAAGG	78514
rs223312618	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77439190	AAGGACTGAGGTCTA[C/T]GGTGTGTAGGTCTGA	78514
rs223344260	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77455012	TGGAAGCTGATGTAG[A/C]GTCTCTCAGAATAGG	78514
rs223351007	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77497606	ACAACATACCATGAA[-/T]TACTCCTGACTCCAA	78514
rs223373074	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77345208	TGCCAGACTGAAGGA[C/T]AATTCTGCCAAGTTG	78514
rs223375687	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77370077	TGAGCGATGATGAAC[A/C]GGAGGCAGTGAATTC	78514
rs223391563	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77386759	AGGGAGGGAGGGAGG[A/G]AGGGAGGGAGGGAGG	78514
rs223402244	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77454495	CTTGTCGCCTAGCAG[C/T]CACAGTAAACTAAGA	78514
rs223417766	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77463491	AGAGACTGAGATGTT[A/G]TGAGCTGCCGTGTTG	78514
rs223417936	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77349000	AGGCTACAGAGAATG[A/G]ACTACCTCGTAAGCT	78514
rs223419509	in-del	-/CTATATCC			intron-variant	Arhgap10	Mm_Celera	8:77399999	GCCATTACACAGGGT[-/CTATATCC]CTATCAGTGTGGATA	78514
rs223420475	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77361517	GTCCAACAAAGTAAA[C/T]GAGAAAATATTTTAA	78514
rs223425805	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77338378	ATTTGGGTCATAATG[A/G]CAAGGAGAAGAGACT	78514
rs223431263	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77462811	AGGCCTGGCTTTTTT[C/T]TTCTCTCCTCATAGA	78514
rs223432182	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77409183	GAGAACATACGCTCA[A/G]ATGTGCGCAAGGCTG	78514
rs223439153	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77317247	AAATCTAGCATCAAC[C/T]CTGACCGAAATGTCC	78514
rs223450384	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77460267	GGATCCACGGTATAC[A/G]GCCTCAGCACAAACA	78514
rs223461926	in-del	-/AAA			intron-variant	Arhgap10	Mm_Celera	8:77512491	TGTATTTTTAAGGAC[-/AAA]AAAAAAAAAAAAAGA	78514
rs223464965	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77261913	GTGGCTGAAGATGAG[A/G]CACTGTGCCACACCC	78514
rs223471068	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77255240	AGCACACCAAGCAGG[A/T]GGTTTTGGAATACAC	78514
rs223510142	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77433407	GTGTGCATGTCCCTT[C/T]TCTTGGCCTCACACA	78514
rs223526287	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77502568	TCAAACAAGCCAGGT[A/G]TGACGTGTAAACCAT	78514
rs223530407	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77410544	CTATTCATCTCGTTG[A/G]CTGAGCAGCTAGCTC	78514
rs223530651	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77320553	AGACACAAGGACACA[A/G]ACAAAGCTGAGAGGC	78514
rs223537092	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77415468	TCACTGGCTAGCATA[C/T]GCATATACAATGGAG	78514
rs223557766	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77281824	GGAGGCTCTGAAGAG[-/A]AAACATCGGAGCTGA	78514
rs223573028	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77418352	CTGTGTCATTCCAGA[A/G]CCTGGGCTAAATCGA	78514
rs223579854	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77501919	AGATAAAACCCTGAC[A/G]GGACGGATCCTAGTA	78514
rs223582972	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77385790	CCACCTTACAGAGAC[A/T]GGCTGACAAACTGCT	78514
rs223586801	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77323461	CAGGAATTTAATCTT[A/T]CTTTCGTACACCTGT	78514
rs223594918	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77438207	TGCCACCCCAGTTCA[C/T]TGTTTCCACGTGTAG	78514
rs223606519	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77504785	AGCATGGCACACTGG[C/T]CAGCATGGTCACAGT	78514
rs223622071	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77309446	GCCTTTCTGGCCTGT[-/A]AACCCGAGTACAGAA	78514
rs223623248	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77512150	TATCTTGAGTGTGTC[A/G]CAAACAAAGGTAAAG	78514
rs223626023	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77286502	GAGGAGCAAGGCAGC[-/T]TGGCAGGCAAGCATG	78514
rs223631890	snp	A/C/G			intron-variant	Arhgap10	Mm_Celera	8:77323986	AAAAAGACTCCCTCC[A/C/G]CCCCCCCCATCCCCT	78514
rs223640223	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77479268	AAAAAACTTCAATAG[C/T]ATTTCCCCTGAAAGC	78514
rs223650413	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77511328	CAAATCCCAGCAACC[A/G]CATGGTGGCTCACAA	78514
rs223651458	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77507545	AAGGCAGTCTGGCAC[A/C]GCATTCTTAAGAGAT	78514
rs223656395	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77401606	TTTTGTTTTATTGTT[G/T]TTTTTTTAAATAAAT	78514
rs223656561	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77398114	TGGAAGCCCTGGAGT[A/G]GACTCTCAACTCCCG	78514
rs223659240	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77315421	AACACCAGTCAGGTT[A/C]GGCTTTGAGGATTTT	78514
rs223662926	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77431154	CTAAACTGCAAGTTC[C/T]TCTCTGGTTCTTACA	78514
rs223677094	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77318307	TGTGGCTACATAATG[C/G]AACTCGGCTTCTGGG	78514
rs223687318	in-del	-/AAA			intron-variant	Arhgap10	Mm_Celera	8:77467708	CACACACACACACAC[-/AAA]GGCTGATCTCTTCTA	78514
rs223699414	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77335823	CCAAGTTTTGGCTAT[C/G]CAGAGGTAGCAGGGA	78514
rs223700858	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77295125	AGGAAAACAGGAGAG[A/G]TCACTTTCATCTCCA	78514
rs223702449	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77287460	GAGGGTGATGGGAAG[A/T]GCTGTGAGGCCTACT	78514
rs223703864	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77291478	ACATAACTGTTTGCA[C/T]GTTTTATATACACAC	78514
rs223706136	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77283788	GGACAGACAGACAGC[C/T]AACATGTAAGAGCCA	78514
rs223708568	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77442331	CTCTCCTCTGCAGGT[C/T]TCCTAACAGAGCAGT	78514
rs223731892	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77284267	TCCACACTACATTCA[A/G]ACAAAACTCTGCGGT	78514
rs223740325	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77329239	TCCTTATCTAGGGAG[-/C]CCTCCAGGCACAGGA	78514
rs223777102	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77362122	CCTGAGGAGAGGATT[A/C]GGAAGGAAAAGGAGC	78514
rs223781785	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77336011	CACACACACACACAC[-/AA]ACACACACCTACCTA	78514
rs223783072	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77261788	ACTAATCAGGAAGGG[-/A]GAAGGGTGGACAGTA	78514
rs223788797	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77462038	TTATTGATTCACAAC[A/T]CTTAATTATGAAGAT	78514
rs223791444	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77317681	TTTATAGCTAACCAC[A/G]ATTTCTAAAATGTAT	78514
rs223797328	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77397843	CCTCTGGAACCGAAA[C/T]GTTCGGCAGCACCAC	78514
rs223798141	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77510659	GCAGGCCAGGACCGC[C/T]CACCAGCTCTGGGAC	78514
rs223802577	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77431769	CACAACCCAAATGCT[A/G]TGTGGAAAAAAGTAA	78514
rs223805845	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77262887	TCCAGGAAAGAGCTT[A/G]AGGCTCTTGGAGAAT	78514
rs223808824	in-del	-/ACAC			intron-variant	Arhgap10	Mm_Celera	8:77475616	GCATAAAATAACTAA[-/ACAC]ACACACACACACTGT	78514
rs223827083	in-del	-/TTG			intron-variant	Arhgap10	Mm_Celera	8:77440316	ACTGGCAGGGGGCCA[-/TTG]CCACCTGGGCTGAAG	78514
rs223832497	in-del	-/TG			intron-variant	Arhgap10	Mm_Celera	8:77414768	ATTTGTTTATTTGTT[-/TG]TTTATTTATTTGTTT	78514
rs223847841	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77321670	TTGTCCTTGTTTTTA[C/T]TTTTTACTTAATTCT	78514
rs223861559	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77410122	ATTTACTGTAACAGC[A/C]AACTCAGGCTCAAAG	78514
rs223870136	in-del	-/AACA			intron-variant	Arhgap10	GRCm38.p3	8:77455328	ACCCCCTTGTCAGTG[-/AACA]ATCAAGAAATGAGCC	78514
rs223879398	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77412307	GTGTGTGTGTGTGTG[C/T]GTGCACACGTTCATG	78514
rs223884532	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77460579	AGGAGCAAAGGCACA[A/G]GTGCACCTGCAGTTG	78514
rs223894238	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77289557	GCCCCAGCACAGCAC[A/G]GGCTTAGCATGCAAG	78514
rs223907295	in-del	-/AGAAAACAC			intron-variant	Arhgap10	Mm_Celera	8:77430575	CCCACCAAGCCTACA[-/AGAAAACAC]AGAAGAACCTTCAAA	78514
rs223907839	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503894	CGGGGAGCTACCCAC[C/T]AGAGAAAAACAAAGA	78514
rs223909438	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77368055	TCTTACAGGAAATGG[C/T]ACATTAGACATCCGG	78514
rs223910644	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77418753	AGCCTATAGGCCACC[A/C]CTCCAGGGGTCAAAG	78514
rs223914070	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77412674	AACTTTTTGACGGGT[C/G]CTGAGGATCTCAACT	78514
rs223914935	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77386623	GCAGGGCTGACCAGA[A/G]TGAGCAGAGGTCTTA	78514
rs223925043	in-del	-/ATCCTTCCCATTGGCTGACTCCTAGA			intron-variant	Arhgap10	Mm_Celera	8:77338569	TGCCTAACTCCTAGC[-/ATCCTTCCCATTGGCTGACTCCTAGA]ATCCTTCCCATTGGC	78514
rs223926555	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77260419	AATTTAAAGTGTAAA[A/G]AAATGGTTCCGTGGT	78514
rs223936432	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77367282	GACAACTGCCACCTA[C/T]AGGCGAGGGGGAAAC	78514
rs223939144	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77323076	TTTCACAAGGAAGAG[C/T]GGCTAGTGTCCCAAA	78514
rs223939982	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77266871	GGGATTCCCACTTGC[C/T]TTCTTCCAAAATGGG	78514
rs223942794	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77279370	GCACACATTTGTGTC[C/T]TGAGCTACCACCACT	78514
rs223948818	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77510121	ATGCCTGGTGTACAC[C/T]CCGGTCAGAAGAGGG	78514
rs223953164	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77436867	CAGTGGAGGAACCAC[C/T]GAGCTGGGACACACT	78514
rs223957119	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77322396	GTCAGAAGAGAAAGA[C/T]GCTGATCTAAGCAAG	78514
rs223973675	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77266856	CATTGGTTTACCACA[A/G]GGATTCCCACTTGCC	78514
rs223976813	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77281628	TCCCCAGCCCAAAGG[A/T]GCTCACATTTAACAT	78514
rs223981101	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77290243	CAAAAAAAAAAAAAC[C/T]AACAACAACCAAACT	78514
rs223991716	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77402663	GCAAAGCATTAGCAA[C/T]TCTGTGAGTTCAAAC	78514
rs223994745	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77480632	TGCTCGTATGTACAT[C/T]TGTGGACCAGCTATG	78514
rs224021402	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77282647	CACACCAAGAGACAG[C/G]CCCAGGAGCGATTTG	78514
rs224033038	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77261141	GCCCCTTTAACTCGG[C/G]TGTTTCCACCACACA	78514
rs224034459	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77396697	GGGCAAACGCTCACT[C/T]ACTGGCTGAACTGCG	78514
rs224040108	in-del	-/CGTGAGCG			intron-variant	Arhgap10	Mm_Celera	8:77279341	CAGTTCTCTTCTGCA[-/CGTGAGCG]AGGGAGCGAGCGAGC	78514
rs224046594	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77491312	AAATAAACAAAGATT[A/T]AAAAAAAAAAAAAAA	78514
rs224054308	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77486498	CACTAAACCTAGACA[A/G]TGACAGCAACTTTTG	78514
rs224059148	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77480114	CACCCTCCAGGCCAC[A/G]GCCCGAGTCCTTGGG	78514
rs224060979	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77346578	ACAGCTTCATGCATG[C/T]ATGAGGCCTGCCTTT	78514
rs224064421	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77397064	TTGCTCTGCCCCACT[A/T]TTTTTCACTGATGAC	78514
rs224065459	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77263067	CAATTCACCTTCATC[A/G]GCTAGCTTTTTAAAG	78514
rs224075945	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77293310	CCAACAGCTGCAGGA[C/T]GCAAGTGATGACACA	78514
rs224085767	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77362817	CAGCAAGCAGTGAGG[A/G]CATCTATTTTGTCAA	78514
rs224094394	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77339234	CTAAGACAAACTCGA[C/T]GACCTCCTGTCTCCA	78514
rs224106697	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77383839	ACATCTGTCAGCATC[C/T]GGGGCCAGGCTGCAG	78514
rs224108389	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77398436	AGTGACCCTTGACAT[A/G]GGAAACCGGTTCCTT	78514
rs224108853	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77455494	TCTGGAGCCCCTGTA[A/G]GATAAGTGAAGTTCC	78514
rs224119906	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77460614	TGCACAAGCATGCCT[A/G]TGGTGCACCAGCCCT	78514
rs224127030	in-del	-/CT			intron-variant	Arhgap10	Mm_Celera	8:77343431	GGACTCCTTGAAAGA[-/CT]CTATTTTTAAAAGAC	78514
rs224127108	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77263586	AATCCTTCTCCCTGG[A/G]CCTCTTTATGCCTCT	78514
rs224132580	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77286157	TCAACCAGCCAACCA[C/T]TAGCTCCTGAAAGCT	78514
rs224133575	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77339555	CTGTAGACCTTAGTG[C/T]ATAACTATGGGTTCA	78514
rs224146693	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77397905	AGGAGAATGCAGGCC[A/G]AGCAGCACCCACCAC	78514
rs224147970	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77418070	TTCCAAAATATATAG[A/G]AAAAAATGTTTCCTC	78514
rs224152306	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77294256	TTCCAATTCCAGCAT[C/T]CAGTGCCATAAAAGC	78514
rs224153829	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77398794	AAATGTAAAGGCCTT[C/T]ATGACTTGTGTCATC	78514
rs224193284	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77461005	AGACAGAGGGGGTTC[G/T]ACATCAGCCTACACC	78514
rs224197572	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77286662	CAAGAAGGGACCAAA[C/T]ATTCAAACTTATTAG	78514
rs224199786	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77372624	TGTGTGTACACTGAG[A/G]CAGTGTCAGGAGCAT	78514
rs224202037	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77455085	TGAAATGACTAAATA[A/C]CCCGTTACAGTTTCT	78514
rs224211703	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77255531	TTACAGCTTCCAGAG[-/A]AAGTCAAAGGGCAAG	78514
rs224218875	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77386099	CAAGTCAAGCAGATC[A/G]TGAGTTCAAGACTAA	78514
rs224224535	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77505949	ACACCCAGTTTGTGT[C/T]CACCAAGCTGAATAT	78514
rs224227841	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77504614	GCTTACCATTTCAGA[A/G]GATCCATCATCACGG	78514
rs224231074	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77417757	GAGAGCCTATGGCGC[A/G]TGGCTGAAGTGGAGA	78514
rs224237562	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77479363	CAGCTTCCATCTTGG[C/T]TAGTGCCTGAGGAGG	78514
rs224239767	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77483447	AAAAGAGGTTAAGGC[C/T]GGCCTAGGCTACAAT	78514
rs224252112	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77462279	AGGGAGGGAGGAAGA[A/G]AGGGTGGGTCTTCTT	78514
rs224257495	snp	A/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77366572	TAACTCACTGTTATG[A/G/T]ACAGACTAGCTGGGC	78514
rs224281463	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77321609	ACAGACACATAGATA[C/T]ACTGCTAACAATTCT	78514
rs224298752	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77401086	TGTTATCATTCACAG[A/T]GCCTGCCAACTCTCT	78514
rs224301728	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77320507	TTCTTATTCTTCTCT[-/C]CCCCTACATAAGCAG	78514
rs224308820	snp	C/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485218	CAAGGGAGCACGCGT[C/G]CGGTGACCCTGCGCG	78514
rs224314045	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77416840	CTCCTGGAGTCAGAG[A/G]CAAGGTTTGCCAGTA	78514
rs224315892	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77461282	GCAATTCTGCAAGAC[A/G]CAGATACGGTCATGG	78514
rs224324927	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77259001	TTCCTAAGAGGGATG[G/T]CACAGCCCTTGCGTG	78514
rs224334386	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77473835	GACAGTAATCAGTTC[-/G]GGATTCTTATGAAGT	78514
rs224336595	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77369198	TCAAACTCAGAAATC[C/T]ACCTGCCTCTGCCTC	78514
rs224340134	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77266085	GACAGCTACAAGGGA[C/T]AGTAATCACACATAT	78514
rs224343088	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77460205	CATGGCCGGGAGCAT[C/T]ATGGGAAACTAAAAA	78514
rs224353774	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77266422	TAAGGGGAAGCAGCT[G/T]ACCCCTTGCTACTTG	78514
rs224356908	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77367527	CCCCAGCAGCAGAGA[A/C]TCCCTCCGTAAGGAG	78514
rs224357285	in-del	-/A			intron-variant, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77517218	TCCCAAAGCATTTCC[-/A]AAAAAAATTACTTGG	78514
rs224359876	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77416156	GAGCACACTACCCAG[A/G]TGTTTGGGAGGATTA	78514
rs224374065	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77462767	GGGCAGAATATAAGT[-/A]AATTGGGTCCCTAAG	78514
rs224375407	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77483573	TCAGCAACAATTGTT[-/C]CCTAAGTCTTGCAGG	78514
rs224380771	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77459821	GATTAACCATCACAA[G/T]GAAGAAACACAATTA	78514
rs224390263	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77259977	AAAGCTGCAAATACC[A/G]TAAACTGAGACTGAC	78514
rs224396311	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77268825	CAAGTTTCCAGTCCC[A/T]TGGCCCTCCTCGGGA	78514
rs224398778	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77396315	ATAAAGATGAGCCCC[A/G]CTCCTCATCAGGAAA	78514
rs224414842	snp	C/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77502621	GCAACCAATCTTGGA[C/G]TCCTCAACCTCAGAA	78514
rs224425821	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77488017	CAGCGCTGTGTGCTA[-/C]CCTCAGAAGGTGGCT	78514
rs224434349	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77345396	GATTGGAAATGAAAA[C/T]GGAATCTCCTAAATT	78514
rs224436110	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77407876	TGCAAAAAGGAGCAG[-/T]TTTTGCTATATATAT	78514
rs224437299	in-del	-/GCCTTAGAGGCA			intron-variant	Arhgap10	Mm_Celera	8:77435236	CTGCCATAAGCAAAG[-/GCCTTAGAGGCA]GGGAAGCCAAAAGAA	78514
rs224447230	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77347661	ATTATCAAAGGTTTA[G/T]AACTCTGGAGGCTTT	78514
rs224447328	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77340025	GTCCAAGCCCAAACA[A/C]TGCCATCTGGCTGTG	78514
rs224453004	in-del	-/CG			intron-variant	Arhgap10	Mm_Celera	8:77411546	ATAGACACATGCACA[-/CG]CACATGTACACACAC	78514
rs224455842	in-del	-/AAAAC			intron-variant	Arhgap10	Mm_Celera	8:77497085	AAAAAAAAAAAAAAA[-/AAAAC]CAGTTCTGCCACAGA	78514
rs224460943	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77436334	CCAATCAAATCCCCA[A/C]GGCTGTGACTTCTAT	78514
rs224475592	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77485918	ACCCTTTCACAGGGG[C/T]CACTTAAGACCACCA	78514
rs224496225	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77477917	TGTCCTACAGTCACT[A/T]GTGTCCTTGGTTCAG	78514
rs224505112	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77340607	CATGCCCTTACTCTA[C/T]TGGAGCCCTCCCTCC	78514
rs224506392	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77478285	AGCGAGGAGGGAAGA[A/G]CAAGACTACCAAAAG	78514
rs224510735	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77371467	GTTTAGTAAGCGAAC[G/T]TATGCTGTAAGCATA	78514
rs224523125	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77443280	GTCAAGTGGTTTATA[C/G]CATTTATGGTATAAA	78514
rs224527084	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77326681	GATAACTGTATAGCT[C/G]TAATGTTCCTCACCC	78514
rs224527197	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77285254	GCGTGTGCGTGCGTG[C/T]GTGCGTGTGTGTGTA	78514
rs224528064	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77442498	GGTTCCAATAACACT[A/G]TAGTTTAGACAATTG	78514
rs224531647	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77443664	TTAATATTACTTCAG[A/T]AACATTATAAAACAT	78514
rs224576139	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77365774	ATCAGGAAGCTACAG[G/T]AGGGAATCAGGTTAG	78514
rs224588640	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77321122	GTAAGCAGTTCTCAG[A/C]CCCCTGGGCCCTGCC	78514
rs224589653	snp	C/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484258	GGACTGAACACGGGG[C/G]CTCACACACGCTAAA	78514
rs224590191	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77373890	CAGAGATGCAGTCTG[C/G]TACCAGCCTTTCTCT	78514
rs224601506	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77448066	AGCTACCAAGCCCTC[A/G]GATTTCAACCAATAA	78514
rs224603597	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77441926	CATTGACTTAACTAG[A/G]TCTCTAAACAAGGTT	78514
rs224612833	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77352293	GCATTAGGAAGGTTG[A/G]GAATCACTGATAAAG	78514
rs224619510	in-del	-/GAG			intron-variant	Arhgap10	GRCm38.p3	8:77254190	TTCCTCCAGCTTTCA[-/GAG]GAGAACAGACCTTGT	78514
rs224632072	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77499014	CCGCTGCCCGCTGCC[-/C]GCTGCCTCTGCCTCT	78514
rs224653598	in-del	-/ACTCATCT			intron-variant	Arhgap10	Mm_Celera	8:77476678	GTTAGGAAAAGACTC[-/ACTCATCT]ACTCATCTACTCATC	78514
rs224654343	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77388617	AGCAAGCCAGCTGAG[C/T]GTATCTGAACTAGAG	78514
rs224656129	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77338519	GGCTGACTCCTAGCA[-/T]TCCCCCCATTGGCTG	78514
rs224657525	snp	C/G/T			intron-variant	Arhgap10	Mm_Celera	8:77441473	AGCATGCCACAAAGG[C/G/T]GGGGGGGGGGGGGGG	78514
rs224671186	in-del	-/TC			intron-variant	Arhgap10	Mm_Celera	8:77328433	GTGCTGCTTTGAGCG[-/TC]TCTGTTTTCTTAGTT	78514
rs224673112	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77372321	TCTCTCCTCATGGTC[C/T]GATTCTTAACAAAAG	78514
rs224676665	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77344518	AAGACAACTGAATGT[C/T]AACTTCTGGGGAATA	78514
rs224684903	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77442459	TCATCGAGAAGTATG[C/G]GCCATGAGATAGTCA	78514
rs224697867	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77291663	CACACAGTGATGAAG[C/T]TCCAGAGCCAGACCG	78514
rs224710367	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77321157	CCACCACGCTGGACC[A/G]TGTCAGATAAAGGAA	78514
rs224711783	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77411237	AGGGGCAGGGGCTCA[A/G]CCAAGCTTGGGGACC	78514
rs224713227	in-del	-/AAAAAAAA			intron-variant	Arhgap10	Mm_Celera	8:77497067	CCCTGTCTCAGAAAG[-/AAAAAAAA]AAAAAAAAAAACAGT	78514
rs224719735	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77343737	CTTTGCTTTTCTTAA[C/G]AGGAAGAAACTTAGT	78514
rs224723461	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77430064	TCCTGGAAAGAAATG[-/T]TTTTTAAAATGTGAC	78514
rs224735444	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77466187	TAGAAGGTTAGTCCC[G/T]CATGAAAAACTGTGT	78514
rs224741581	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77417796	GAAAGCAGAGACAAG[A/G]CAGGAGCGTGGGGCT	78514
rs224779555	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77284489	CTTCACAAAGAATTA[C/T]GAACTTGAACTTGTA	78514
rs224789418	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77504186	GCTGGCAGTTCTAAA[A/G]AGCATGGTGTCACCA	78514
rs224801295	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77417192	CGTCACAAAAGTGCA[A/C]AGCGAGCTTTCTAAA	78514
rs224804580	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77465210	TCAGGTACAAGGTGT[A/G]TTCAATGGAACAGGC	78514
rs224807467	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77464159	CCTGGGTTTGATCTT[-/A]AAAAAATGATAATAA	78514
rs224813330	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77270511	TGGTGCTTCCTGGAC[A/G]CAACAGGGCAAATGT	78514
rs224828339	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77353192	ATATCCAAAGCGGAA[C/T]GCAGTGAGTGCTGAG	78514
rs224842224	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77319855	CCAGTCCAGGCACCA[G/T]ATGTGGATATAGCAG	78514
rs224853180	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77438301	CCTCTCTCCAGGGCC[C/T]CACTCCCGTCCCTTC	78514
rs224855164	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77440944	AGTCTCTGCCTGCTG[C/T]TGTGCCCCACCAACA	78514
rs224882692	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77345136	GGAAGTCCCCAAGAC[A/T]GTGAGCTCTCTCAGA	78514
rs224883636	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77327901	CCTACTTGGATCTCA[C/T]GTACCATACATAAGC	78514
rs224896141	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77264719	TAGGGAGAATAAATA[C/T]TCTTGCTTTAGAGAA	78514
rs224906673	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77292222	CTCCTTCATAGGCAG[A/G]CTCACAGTAGGGAGT	78514
rs224909478	in-del	-/G			intron-variant	Arhgap10	GRCm38.p3	8:77370103	AATTCACAATCCTGA[-/G]GGGGGGGGGGGCGGG	78514
rs224911146	in-del	-/CCAGGGAAAGCATAGAGGGGCAGGGGCTCAA			intron-variant	Arhgap10	Mm_Celera	8:77411207	TACTGCCCTGCTCAG[lengthTooLong]CCAAGCTTGGGGACC	78514
rs224911842	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77437393	CGGCATAAAGGCACA[C/T]GTTTGCAATCCCAGG	78514
rs224920695	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77507687	CTCTACTGCCTTCCT[C/T]TATGCTCTGAAAGCA	78514
rs224930034	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77421364	AGAATGACAGAAGGA[A/C]GGACGGTAGGGCTGG	78514
rs224932303	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77447231	GGCTCCCGAGTACTG[A/G]GATTAAAGGCATGCA	78514
rs224942132	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77322004	TTTTCCCAAGCAATA[A/G]CAACAATGTGGTGAG	78514
rs224953139	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77325874	GCACCCTACTGTGCA[A/G]AACAACAAAACCTAC	78514
rs224963364	in-del	-/CA			intron-variant	Arhgap10	Mm_Celera	8:77411543	ACACATAGACACATG[-/CA]CACACATGTACACAC	78514
rs224966489	in-del	-/TGT			intron-variant	Arhgap10	Mm_Celera	8:77339572	TAACTATGGGTTCAA[-/TGT]ACACAGACAAATGCC	78514
rs224966620	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77444039	TGCCCAGACCTCCTG[C/T]GTCTAAGGTGCCTCT	78514
rs224981047	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77400460	GGTAGATCTTACTCT[A/T]TTCCTGAGCATCTAT	78514
rs225004911	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77514920	CTCAGATTAAGTGCC[A/G]AAACCATCCGTAAAG	78514
rs225011153	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77315931	GTGGTATGGCAAAAT[-/G]GGGCAGGGGATGGTA	78514
rs225013285	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77474684	GTGGACCCAAAGAAG[-/C]TGAAGCGGGTAAAGC	78514
rs225016147	snp	A/G/T			intron-variant	Arhgap10	Mm_Celera	8:77459194	TATTTTCGTTAAAGT[A/G/T]CTCATTTGACTCTCT	78514
rs225019248	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77326360	ACCACCCACATGGTG[A/G]CTCACAACCATCTGT	78514
rs225019914	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77421083	CAGGCGCACACACAC[-/T]ACACACGATGAAATA	78514
rs225029775	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77292875	CTAGGGGGCTGAGCT[A/C]GCTGCAGGCTTCAGA	78514
rs225044859	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77396364	TGCATTATAGTCAAC[A/G]ACGCAGTGGTAAGAA	78514
rs225044889	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77516285	ACTCATCAAAAAAGT[A/G]ATTTCCAGTCCCAAC	78514
rs225046548	in-del	-/CCC			intron-variant	Arhgap10	Mm_Celera	8:77253113	CTAGAACCCCTGCCT[-/CCC]CTCCTCTGAGTGTAC	78514
rs225054813	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77421543	AAGATAAATATTTTC[C/T]AACACATTTTCAGAA	78514
rs225070033	snp	A/C/G			intron-variant	Arhgap10	Mm_Celera	8:77370115	TGAGGGGGGGGGGGG[A/C/G]GGGGGAATAGGAAAG	78514
rs225089447	in-del	-/ACACACAC			intron-variant	Arhgap10	Mm_Celera	8:77475615	GCATAAAATAACTAA[-/ACACACAC]ACACACACACACACA	78514
rs225093265	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77320670	AAAGTCCCTAGACTA[C/T]CAGTTCAGTGGTGTG	78514
rs225095535	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77299361	acccagaaatgaacc[C/T]acacacctatggtca	78514
rs225096089	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77375491	GTAAGCACATCATAA[C/T]AAGGACCAGAAAGGG	78514
rs225099578	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77464462	AGGACGATTTCATAA[A/G]GTCATGCAGAAGCTA	78514
rs225108177	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77320242	GGGTTACACAGAGAA[A/G]CCCTGTCTCAAAAAA	78514
rs225109492	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77285586	TAAAGGAAATGGAGA[G/T]GGAGTAACCGAAACA	78514
rs225113384	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77372451	GTACTTGCTTAACAA[C/T]CTCCTGAGTTGTTTG	78514
rs225121109	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77483494	ATGAAACATTTAAAC[A/G]CCTAAGAAGCTGAGT	78514
rs225126801	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77400063	ATCCTTAAGATCAAG[A/G]AATTGAAGTCTCCAA	78514
rs225127556	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77447824	ATCATCATCATGGTA[G/T]CGAGCAGCCAGACCG	78514
rs225129584	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77290487	AAAGGGAAATAGGCC[C/T]TGAGTGAAGCCTCAC	78514
rs225130769	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77435564	TTAAATCTCATGGAA[C/G]CATTTTCTCACCTGA	78514
rs225132818	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77298129	GCTGCCATGCTTCCC[A/G]CCATGATGATAATGG	78514
rs225134455	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77507642	ATATTCCAGGATCCA[A/G]ACTCCGATCAGGAAG	78514
rs225136958	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77468835	AATCTTTTACTTTAC[A/C]TGACCCTTTTACAGG	78514
rs225146001	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77265211	ACTCGGGAGTGCGTG[A/G]TTCTCACCACCTCAC	78514
rs225166600	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77413637	CCGTGTCTGAAAAAG[-/AA]AAAAAAATACAGATT	78514
rs225179231	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77440252	AGCATTTCATCACCA[A/G]CAAAAGGGGCTGGGG	78514
rs225182802	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77512804	TTGTCAGAAATGGCA[A/G]GGAGCCCTGCCAGAT	78514
rs225197367	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77265554	GTCCAAAACAGACCC[C/T]GTCCACTCATTACTT	78514
rs225211689	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77388093	AGAAATCAGTGCTGG[A/G]ACCGAGTGCCAACCG	78514
rs225215242	in-del	-/CTGTCACTGTCA			intron-variant	Arhgap10	Mm_Celera	8:77314660	AGCACAAACAGAGGT[-/CTGTCACTGTCA]CTGTCACTGTCACTG	78514
rs225225293	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77345430	CATAGTCCGTTTCAC[-/A]AGCATAAGTCATATT	78514
rs225233948	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77291085	CATTGTAACTCAATC[A/G]TGCTTCGCAAAAACT	78514
rs225248166	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77400803	TCTCTATTTTTAAGA[A/C]AACTCTTCTGCCTCA	78514
rs225254524	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77350309	GCCTGGCTTTTTCCA[A/G]GCTCTAAGACAAACA	78514
rs225258097	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77414831	ATGTACACACACAAT[A/G]CTACACAGAGAAACC	78514
rs225260830	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77463338	GGCAAACTGGATACA[A/G]TCATCCACTTTATAA	78514
rs225271570	in-del	-/GGAA			intron-variant	Arhgap10	Mm_Celera	8:77330685	AGAGGGAAACGCCAG[-/GGAA]GTAAGTAAGTTCCCT	78514
rs225283594	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77265842	GAGGTGTGTGTGCTC[A/G]GCCCAGCTTGTCTAT	78514
rs225285912	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77375024	CTAATCCTCCGGTAT[C/T]TTTCCTATAGCATGA	78514
rs225298146	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77422441	AATGAATGAATGAAT[A/G]AACAACTGTGTATTA	78514
rs225298410	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77297114	TAGGGGGAAGACCTG[A/C]ATGCCTCCTTTCACA	78514
rs225303243	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77401121	GTTATACATTAATTA[C/T]AATGGTTTTTCACTT	78514
rs225308596	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77415134	TCTCCTGTTGCTTAA[C/T]GCTACTGCCCTAAAT	78514
rs225308645	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77421601	CTGGTACTTTTAATT[A/G]AAAGTCTTTGAGTAA	78514
rs225316169	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77421020	AGTCAAAAGCCCCGT[C/T]GACACCACCTGCACA	78514
rs225320261	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77506330	CATTGTTGGTTCTCC[C/T]GCGCCTTCCAGAGGC	78514
rs225331166	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77270030	GAATAAGGAAAGAGT[A/G]GACAGTCAAGTCAGG	78514
rs225335962	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77290028	GACAGACGTGGGAGG[A/G]GCTGGAAGGAGGAGA	78514
rs225337905	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77463796	GTCTTTAAAGAGTTT[C/T]CAGAAAGTCAACAGG	78514
rs225342456	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77469611	AGCGCACTAGCTCCC[A/G]AGTTCAATTCCCAGC	78514
rs225351589	in-del	-/TC			intron-variant	Arhgap10	Mm_Celera	8:77410441	GTTCACCTTAAGCAA[-/TC]TCTCACAGCTATTCA	78514
rs225364871	in-del	-/TAA			intron-variant	Arhgap10	Mm_Celera	8:77333822	GAGTCACCACTGAGC[-/TAA]TAAAGCTTCAGGAAG	78514
rs225366129	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77396005	GATCTGTGTCCATCT[A/T]TACAAGATTTATTCA	78514
rs225368046	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77513363	AAAGGAGTCTCCGGG[A/G]TCCACGAGAGCATCT	78514
rs225372707	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77425374	aagaaggaaaagaag[A/G]aggaggaggaggagg	78514
rs225379294	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77506762	CCTCTGCGGAAGCTG[A/T]CCATTTTAAAGGAGC	78514
rs225382228	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77324992	CCAATGCACTGTAAT[A/G]CATGGGTTTGTGAAC	78514
rs225383264	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77486739	CCCTCTCTCTCTTTC[C/T]CTCCCTCCATCCCTC	78514
rs225383360	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494896	ATTAAAGGAGACAGT[A/G]GCAGCACCTCGGGCT	78514
rs225390871	snp	C/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485840	GCCAAGCACTATGAA[C/G]TGCCCAGTCCTCTAG	78514
rs225392511	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77404913	TGGGATTAAAGGCGT[A/G]TGCCACCAAGCCTGG	78514
rs225398371	in-del	-/AACGAC			intron-variant	Arhgap10	Mm_Celera	8:77426657	TCTTTCCCAACCCTT[-/AACGAC]ATTCAACTCTTCATA	78514
rs225400797	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77464574	CTGGATTCCTTCCTT[A/G]TTTGCACAGGTTTCC	78514
rs225402706	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77369497	AATTAAACCAAACTT[A/C]TAAAGATTAGGGCAA	78514
rs225421806	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77376038	ACGCAGTCCCAGCAC[A/G]ACTTGAAAATCAGCT	78514
rs225426027	in-del	-/CAT			downstream-variant-500B	Arhgap10	Mm_Celera	8:77250282	GGTTCTAAGGACTAA[-/CAT]CATGGTCTGCTGACC	78514
rs225427512	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77269997	GGGGCAATCAAGAAA[C/T]CAAGCAAACTAAAGT	78514
rs225443487	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77403730	TGCTCTGCTGTTTGT[A/C]CAAACAGACTTGCAT	78514
rs225443919	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77319509	TAATTGCTAAGAGAA[A/G]GGAGACACATTGACA	78514
rs225460763	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77399596	GCTTTCTTTCTTAAA[G/T]CTGTACTTTTGTGAC	78514
rs225462712	snp	A/G			intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77493135	AAAAATTAGTGGAGG[A/G]CTGAGAAAAAGAGGG	78514
rs225463062	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77405075	ACGCTGGCTAATACG[A/G]CACAAGTCTGGTGAA	78514
rs225468085	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77398152	CTACTTCTTTTTTTC[-/T]TTTTTTTTTAAAGAT	78514
rs225469769	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77271001	CAAAACCAAGTGTCT[A/C]GGCACGCAGGAAACA	78514
rs225470442	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77349511	CAGCAACAAAGGCTG[G/T]CAGCGTGGGGTCACT	78514
rs225472910	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77470852	CACAGGGCCCAGAAG[G/T]AGATGTCTGATCCTC	78514
rs225475055	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77488376	AGCTCCAAGTTAGTT[C/T]GGCTTAAACAAACAT	78514
rs225482184	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77268983	GGTCTCTCTGCCAAC[C/T]ACAGGCATTGACAGC	78514
rs225492888	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77371527	GTGTAAAACAAAGCA[C/T]TACCGACAACTAACA	78514
rs225496016	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77296345	ACACGGTGGCTCACA[A/G]CCATCTGTAATGGAA	78514
rs225500828	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77463439	CCTACCTGATGCCCA[C/T]GGAGTCAGAAGAGGG	78514
rs225511675	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77263416	GTCATAATAAAACTT[G/T]GTTTTGTGCAGTTAA	78514
rs225534158	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77400088	CTCCAAAGTGGGGGA[A/G]CTGAGACAGGAAAAG	78514
rs225536910	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77470571	CGTGCTCACAGCCGG[C/G]TCTGCATCTCTGGCT	78514
rs225538262	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77297506	AATTGAAAACAAACA[A/C]ACACAAAATTCAAGG	78514
rs225555841	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77342006	CTCAGTCATATTATT[C/T]CACACCTCAGCCTCA	78514
rs225558337	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77271390	GGAAGTGTAAGCTGA[A/G]TAAACCCTTTCCTCC	78514
rs225599689	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77252386	ACCCAGCAGGCAACT[C/G]GATTTCTTCATCCCC	78514
rs225604926	in-del	-/CTCGATGACCT			intron-variant	Arhgap10	Mm_Celera	8:77339229	CAGTCCTAAGACAAA[-/CTCGATGACCT]CCTGTCTCCACGAGA	78514
rs225609985	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77351870	GCTATTCCCCCTAGA[C/T]GCAGTTAACTCTTAA	78514
rs225614986	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77289414	TGAGACAGTGGAAGG[G/T]GTGTGCCCAGCCTGA	78514
rs225616389	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77418070	TCCAAAATATATAGG[-/A]AAAAAATGTTTCCTC	78514
rs225619595	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77288397	CTGCAGCTTGCGATT[G/T]CTTTGAAAGGGACAT	78514
rs225634187	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77328989	TGAAGCCCACTCCGT[A/G]TCTTCTTTTTCTCAT	78514
rs225635085	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77414353	TGTCTTGATACCAAA[A/T]AGCTGCTGCTGTGAA	78514
rs225636697	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77273924	CAAGAGCTTCTGTTT[A/G]TTGTAAACAAGGAGT	78514
rs225654602	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77369823	TGCCCATCTTCGTGT[A/C]ACCTGTTTACAGTCT	78514
rs225657106	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77375127	AAATACAGTCATCAC[A/G]ATATGCACAACTCGG	78514
rs225662465	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77273006	AGCATAAGAGATATG[C/T]GGTGATATCCAGACG	78514
rs225676043	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77343860	TTCCCAACACGCACC[A/G]TCATGGGGCAGACTA	78514
rs225688296	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77488575	TGCAGTCTGCATCTG[C/G]GGCCAGGGGCAGGGC	78514
rs225690324	in-del	-/AT			intron-variant	Arhgap10	Mm_Celera	8:77425175	TTCCCCCATATATAC[-/AT]ATATATATATGTAAT	78514
rs225703356	in-del	-/ACACACACACA			intron-variant	Arhgap10	Mm_Celera	8:77352684	CACACACACACACAC[-/ACACACACACA]CCCAAATAATGCCAG	78514
rs225711081	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77420461	GGACAGGGGTCACGG[C/T]ATGGCGGGGGGGCTG	78514
rs225719799	in-del	-/ATTG			intron-variant	Arhgap10	Mm_Celera	8:77329283	CCGGTAGAGGAATGT[-/ATTG]ATCGTGGTGGGGACA	78514
rs225721173	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77370205	TCCTAGTGTTGGGGG[A/T]TGGAAGGGTTTAGAG	78514
rs225721470	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77268634	GAACTATACAGGACA[C/T]GTTATGGCCCCCAAG	78514
rs225728788	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77269423	AGCTGAGCAAGCAGA[A/G]ACATAAAGGCTGCAG	78514
rs225740121	in-del	-/CG			intron-variant	Arhgap10	Mm_Celera	8:77466917	ATAAAGTCACACACA[-/CG]CGCACACACACAAGG	78514
rs225746423	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77488081	ACACTGCTACCAAGT[C/T]AAACCGGCCTGGGAT	78514
rs225751536	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77445731	TGGAAGAGAGGAGAG[C/T]AGCCATGCCTGAGAA	78514
rs225757467	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77372693	TCACACTGTCCCTCT[-/G]GCTCTTCCTTCCCAG	78514
rs225768731	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77375648	GTCCCTCAGTGTGCC[G/T]ACAGCCTTGAATCAA	78514
rs225779369	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77348940	CAACCCAGAAAGACG[A/G]GTCCATGCTCACCGC	78514
rs225785587	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77346771	TCCCCCAGAATTGAG[A/G]CTCAGGTTACATCAC	78514
rs225801194	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77294031	TCTTCTCATTCTCCT[C/G]AACAGGAATCGTCTT	78514
rs225813341	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77251494	AGGCCTGCTTCAACC[A/C]ATCAAGCACTACCGG	78514
rs225834508	snp	A/G			downstream-variant-500B	Arhgap10	Mm_Celera	8:77250118	CCAGTCAGGAGGGCT[A/G]GTCATCAGCATAACT	78514
rs225844390	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77349571	AGCAAAGCCAGGAGA[A/G]CTGTGATGTGTCCAG	78514
rs225853890	in-del	-/CATC			intron-variant	Arhgap10	Mm_Celera	8:77481458	GATGTCATACACACG[-/CATC]CATCCCATTTCAAGA	78514
rs225856851	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77445786	CGCCACGTGGAGTAC[C/T]GGGAGAGCTCGTCCC	78514
rs225863768	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77380122	AAAAGATCCCAGGTA[G/T]CAGGCCACTAGCAAT	78514
rs225878668	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77251941	GAGCATTTCTTGACC[C/T]GCTCATGTTTGGAGT	78514
rs225884890	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77404273	TAGCTGCCCCTCCAT[C/T]GGGCACTGGTGTGCA	78514
rs225889506	in-del	-/TCCCAC			intron-variant	Arhgap10	GRCm38.p3	8:77251530	AATCAGGCACACTGA[-/TCCCAC]TCCCACACTGGTTAG	78514
rs225900647	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77443749	CACTCGGGAGGCAGA[A/G]GCAGGCGGATTTCTG	78514
rs225911273	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77418615	TTGAAAGTCTTCATT[A/G]TTTTTAATGTGGGGT	78514
rs225928729	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77462949	AGCAGAGGCTTCCAG[G/T]GTGGCCCAGTGGACG	78514
rs225935303	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77461784	ACAAACTTACTTCAT[A/C]TCAAACCATAGACAG	78514
rs225935473	in-del	-/CA			intron-variant	Arhgap10	GRCm38.p3	8:77421031	CGTCGACACCACCTG[-/CA]CACACACACACACAC	78514
rs225962456	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77350944	AGAACGATTAAGCAG[C/T]ATGCACTAGGGATAA	78514
rs225962911	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77323964	AGGGCCCATTGCTTA[C/T]TGTAGGAAAAAGACT	78514
rs225967353	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77398702	CAGCTTTCCCAAAAC[C/T]TAGTATAAATTCATC	78514
rs225980171	in-del	-/AAATGAGAC			intron-variant	Arhgap10	Mm_Celera	8:77476178	CACAGAAGTAAATCA[-/AAATGAGAC]AATTTTCAAAACATG	78514
rs225980667	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77449803	CAGTTTCTCCATTCA[C/T]AAAACAGGGTGGAGT	78514
rs225983850	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77364222	AGGGCAACTTTTCCT[-/G]GGGTCCGTGGCTTGA	78514
rs225991425	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77419818	GGTTGTTACACAACA[A/G]CTCAGAGCTAACATA	78514
rs225992106	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77468939	TAGTAATGAAAATAA[C/T]GTTATGGCTGGGTGT	78514
rs225993601	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77462649	AATGATAGCTTTCAC[C/T]GTGGAGGTCTTTGCT	78514
rs226001441	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77251277	GCCTTTCCCACTTCA[A/G]GTTCAAACCAAGTTA	78514
rs226003834	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77491545	ATCTGGAAGGCCTCC[A/G]CCTTTATCACACTCT	78514
rs226007392	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77355345	TACATAGCAATGCCT[C/T]TCAGGCCAGAAAAGG	78514
rs226020678	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77266189	GCTTGTGTGTGGTTT[C/T]ACCCCCCTAAACACA	78514
rs226035993	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77461106	CATTGCCAACTTGAG[A/G]ATAAGGAGAGAGTTT	78514
rs226043279	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77439614	TAAAACTTTAAGAGT[C/T]CCCTTCCTAACATCT	78514
rs226044945	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77441083	GCCCAGAAAGGCTTC[A/C]CAAGGGGCTGACGGT	78514
rs226057058	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77468138	CCTCCTCCTTGCAGG[C/T]CATCTGGTCCAAGGA	78514
rs226066197	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77355940	CGTATCAAGGTATTG[C/T]TTGATGGATCCAAGG	78514
rs226072424	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77330599	CCAAAGAGACTGAGC[A/G]GCTGGAGTTAGAGCA	78514
rs226081728	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77472163	ACATATATATATATA[C/T]ACACATATATACATA	78514
rs226082070	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77424289	GGGGGAGGGGGGGGG[G/T]CATGCACTGCAGGGC	78514
rs226101751	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77440611	AGACAGACATGTGGG[A/C]AAAACACCATTGCAT	78514
rs226105485	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77447313	GCCTCATTCCCTCAT[C/T]CGCCTCAGTCAAAAG	78514
rs226120036	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77446395	TCGTGCATCACAAGA[A/C]GTAATCACTACCAAG	78514
rs226122276	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77329618	TAAATTTAATTTTGT[A/T]GTTTTCCCCTTAATG	78514
rs226130458	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77324531	GAGTTGACAGATAAC[C/T]GGCATATGTAAAAAA	78514
rs226130845	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77511016	GTCTGGCAATCCATG[C/T]CCCTGCTCTGTGTAA	78514
rs226137572	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77511252	CAGAAAGGCTATGGA[A/G]GGGCTGGAGAGATGG	78514
rs226140163	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77486256	CTTGGGTGCATCAGG[C/T]TGTCCTTGAACTCAA	78514
rs226149508	in-del	-/GTTG			intron-variant	Arhgap10	Mm_Celera	8:77372019	CAAATGCAGCAGGCA[-/GTTG]GTTTATTAAAAGCTA	78514
rs226152033	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77402524	AGGACTTAATAGTAT[A/G]CACCTATAATTCCAG	78514
rs226157599	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77423991	CTTCTGAAGTCACCA[C/T]CTCCAGGGCTTTCAA	78514
rs226162154	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77447057	GTTTGGTTTGGTTTA[A/G]GGGGGGGAGGGTTTG	78514
rs226174968	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77328631	CCTCCTACCAGAGCA[C/T]ATCTGCACCGCCCAT	78514
rs226176814	in-del	-/AAA			intron-variant	Arhgap10	Mm_Celera	8:77370101	GAATTCACAATCCTG[-/AAA]AGGGGGGGGGGGGCG	78514
rs226176824	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77334773	GACTAGGCCTAGGTC[G/T]GCAGAGACAGGCAGC	78514
rs226178292	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77368870	TTTTTATTTTTTAAC[A/G]TAACTCACAATTAAT	78514
rs226179757	in-del	-/AA			intron-variant	Arhgap10	GRCm38.p3	8:77441014	ACATAGACACAGGGG[-/AA]AAAAAAAAAAGGCTA	78514
rs226179780	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77354323	TAGCTACAACCCAGA[A/G]AACTAGCTGTCTCAG	78514
rs226184489	in-del	-/AG			intron-variant	Arhgap10	Mm_Celera	8:77413196	TGAGAAGGAATGGGA[-/AG]AGAGGAAAGAGCAGA	78514
rs226193202	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77325069	TTCCAACTGAGAAGG[A/G]CGCAGGCATGTGGAC	78514
rs226196436	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77323876	AGGTAACAGAGAATG[C/T]TCTGTGTCTCCTTGG	78514
rs226220271	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77429860	GGCCGCACACTGTGC[C/T]TTCTGAGGCACAAGT	78514
rs226221364	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77369546	AAAGTTAAAGTATAC[-/A]AAACTATCGTTCATT	78514
rs226225707	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77510382	CTGGGAAGTTCAACA[C/T]TCCTCCACAAAATTG	78514
rs226229624	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77296032	TAGGTGTGGTCTTGT[G/T]GGAGTAGGTATGTCA	78514
rs226230320	snp	A/G			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519443	GGAGTATTGGCTTGA[A/G]TAAGAATGATTCCCA	78514
rs226230370	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77309185	GTTTATTAACACTTC[A/T]ACCAGGACAGGTGAG	78514
rs226231371	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77354827	TTTCTTCCCTATGAA[C/T]CCATCCCGTCTTCCA	78514
rs226235487	snp	A/C/G			intron-variant	Arhgap10	GRCm38.p3	8:77329287	GTAGAGGAATGTATC[A/C/G]TGGTGGGGACAAAGC	78514
rs226258950	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77382081	cacacacacacacac[A/T]cacacacacacacac	78514
rs226263025	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77465854	AATATAAAGTTGGAG[G/T]GGGGGGGGGGTCAGT	78514
rs226265862	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77397812	CTGAGCCTCTGGGCA[C/T]GCCAGTGAAGGGCTG	78514
rs226266549	snp	A/C			upstream-variant-2KB, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77518514	CTTAGGACAAGGGAG[A/C]GTGTGGCTAAACCGC	78514
rs226268697	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77444412	ACGCAACCCTGCCAG[G/T]TCTGGCCTCTTACTA	78514
rs226283626	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77406084	GGTGGTGGCCACACC[-/T]TTTAACAGCACTCAG	78514
rs226285817	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77509192	GAACCAAGTGACAAG[A/G]CTAATCTAGTTCCTC	78514
rs226286482	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77347519	GTCTCTGCCTCCCAA[C/G]TGCTGGGATTAAAGG	78514
rs226286672	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77429426	GCTCCACATCCAGCA[C/T]GAGCCAGTGAGCATG	78514
rs226293237	in-del	-/GGTT			intron-variant	Arhgap10	Mm_Celera	8:77407469	ACAGACAGACAGACA[-/GGTT]AATTAATTCATTTAT	78514
rs226293705	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77415933	CAAAAAAAAAAAAAA[C/T]ATGACAGATGCTGGC	78514
rs226293787	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77459204	AAAGTTCTCATTTGA[C/T]TCTCTCACATGGGCT	78514
rs226321664	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77296537	ATGCTAAGCCCAACC[C/T]AGCTAAGCATTCTTC	78514
rs226324202	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77333504	AGGGTTTATTACTGC[A/G]ATGAGAGATTTCCTG	78514
rs226335004	snp	C/G			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77485871	GGCAGGGGTTCTCAA[C/G]CTACGGTCATCTGCC	78514
rs226340331	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77450427	AGGGTAACATACATG[C/T]AAGTCAAAGGCTCTT	78514
rs226344378	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77309568	ATGCCTGACCTCTAA[C/T]ACACACACACACACA	78514
rs226344632	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77293659	ATAAGTGATTAACAA[C/G]TGCTAAGAAATAATA	78514
rs226345989	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77450227	GGTATGGAGCAAAGC[A/G]CCAGGCCCTCGGAGC	78514
rs226348746	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77372483	AGACTGAGAGTACCT[A/G]TGGTAGTCTATAAAT	78514
rs226349722	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77294677	TCTCCCTCCCCAGCG[C/T]ATGCTCATTCCCCTC	78514
rs226356514	in-del	-/ATTA			intron-variant	Arhgap10	Mm_Celera	8:77508400	TATGAATCCCAACAC[-/ATTA]TAATTCTTTATCTTT	78514
rs226358003	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77289482	GACAAAGCAGAAGGC[G/T]TTTGACCCAGGTGCT	78514
rs226362867	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77491938	GCTCCACTCTCATTC[C/T]CCCCCAGCTCTCCAC	78514
rs226363491	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77443939	AAGTGTCAAACACCA[A/G]AGTGGTTATAGCAGA	78514
rs226379899	snp	A/C			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77516977	CTCACAGGCACTTCT[A/C]GCAGGCCAGAACCTG	78514
rs226392064	snp	C/T			utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250670	CTGCCCTCTCTCTGT[C/T]CCACAGGTGGGAGAA	78514
rs226395866	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77408164	AGAAAGGCTGCAGCT[C/T]ACAATCATGTAAAGA	78514
rs226401273	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77267786	ATGTGACTTTTCTCG[G/T]AGATTCCCAAACATC	78514
rs226417827	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77327776	CACGCAGGCACTTCC[A/G]GTTATGAATGCTCTA	78514
rs226419265	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77294157	AGTTATACCATAACT[A/G]TGATTGACCAATCAG	78514
rs226451412	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77403301	AGCACGAGACAGCAC[G/T]AAGGTAAGCATCCCT	78514
rs226453168	in-del	-/ACA			intron-variant	Arhgap10	GRCm38.p3	8:77441500	GGGGGGGGGGACGGG[-/ACA]CACCGGACCTCCAGG	78514
rs226454706	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77272189	TTCTGTATAGCGCTG[C/G]AGAGATAGGGTGGTT	78514
rs226461822	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77272566	CAGCCCAGGGGCTGA[A/G]CTGCCCTTCCCCCAG	78514
rs226470676	in-del	-/TT			intron-variant	Arhgap10	Mm_Celera	8:77324081	AGCAGTCTCCGAGTA[-/TT]TTTTTTTTGTGTAGC	78514
rs226475777	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77424364	GGCTTCCTGCAGAGA[A/G]TGCCACAGGCTGAGG	78514
rs226481678	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77268650	GTTATGGCCCCCAAG[C/G]TCTCTGTGTAGACAT	78514
rs226481894	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77467823	ATCCGCATCAGAGCT[A/G]AGAACTTTCTCACAG	78514
rs226484667	in-del	-/TGTAAA			intron-variant	Arhgap10	GRCm38.p3	8:77430918	CAGATGCCGGCACCT[-/TGTAAA]TGTTCTGCTGTTATC	78514
rs226484775	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77406510	GAGCTGGAGAACAAG[A/G]TTAAGGGGAGGAAAG	78514
rs226491053	in-del	-/TCTGTG			intron-variant	Arhgap10	GRCm38.p3	8:77283933	TGTAAGTGGCAAGAC[-/TCTGTG]TGTGTGTGTGTGTGT	78514
rs226491856	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77272240	TACCTGACCTACACG[A/C]AGCTGGGTTTCATTC	78514
rs226508492	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77353103	GTCAAAGGCAGTACA[G/T]TCTTTGATTTCAATA	78514
rs226536964	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77305937	ACTCCAACACACCAG[A/G]AAAGGAAGACTCAGA	78514
rs226538684	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77497983	GTATATTCAGAGAAG[A/C]GTAACTGAGGAGGGA	78514
rs226546604	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77407016	TCTGCAGTTAAGAGC[A/G]GCAGCTGCTTTCACA	78514
rs226565052	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77253561	CATGACAAATGGCCT[C/T]GGCACAAGAGAACAC	78514
rs226565845	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77266778	CCGAGAAAACACCCA[A/G]CATCCAACAGACATG	78514
rs226574025	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77398405	GGACCGATGTCAGAT[A/G]TCATCGGGTGCCTCC	78514
rs226574500	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77401924	AGTGACCGTCGTCGT[-/C]GGCCTCCTCCTCCTC	78514
rs226575424	in-del	-/TTGCAC			intron-variant	Arhgap10	Mm_Celera	8:77488788	ATGTCACGTGTTCAA[-/TTGCAC]TTTTCTGTACATCGG	78514
rs226578744	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77311727	AAACACTGGAGCCAT[A/G]GGCCTGACAGACGCT	78514
rs226580724	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77252864	TTTCCTATAATGGGA[C/T]CGTCCATTTGTCCTG	78514
rs226600079	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77497276	CTGTCACATGGTGCT[G/T]AGACCTCAACGTGGG	78514
rs226605174	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77402046	CCAACCCTGCACCAC[C/T]CTCAAACACAAACAG	78514
rs226606157	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77467593	CCATGGATCAGATAC[C/G]ATGCACGACCAACCC	78514
rs226609015	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77407468	AGACAGACAGACAGA[C/T]AAATTAATTCATTTA	78514
rs226624966	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77373113	AAACCAGGGGTCTTG[C/T]GTGTGCTGAGTGAGT	78514
rs226625267	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77379154	CTGTGCCCTGACAGC[C/T]TCCTCTAACTCTGCA	78514
rs226633856	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77292648	CACGCTCCGGGGGAG[A/G]CGCGCTTTAGAGGGA	78514
rs226638828	in-del	-/TTTTT			intron-variant	Arhgap10	Mm_Celera	8:77508132	GTCTTTCTAGCTGGG[-/TTTTT]TTTTTTTTTTTTCTC	78514
rs226648153	in-del	-/TTTTTTTTTTTT			intron-variant	Arhgap10	GRCm38.p3	8:77404763	AACCATGCAGAAACC[-/TTTTTTTTTTTT]TTTTTTTTTTTTTGG	78514
rs226653221	in-del	-/GTTA			intron-variant	Arhgap10	Mm_Celera	8:77273296	TGAAGATTAAGCTAG[-/GTTA]ATGCTGAAGACAGGT	78514
rs226664318	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77467263	AGGAAAAGCAAACAT[A/G]CGAATAGTCTATATA	78514
rs226665397	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77402576	AAGTCTGAGGCCAAG[C/G]TGAGCAACTCAGCAA	78514
rs226666249	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77272798	CATTTCACTACTATA[A/G]TTGGTACTGCAAATC	78514
rs226673013	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77298288	GTTTTATATTGGGAA[-/T]TTTTTTAAAGAGGCT	78514
rs226673604	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77308814	CAAAGAAGCCTAACA[A/T]CAGTGATGATTATGG	78514
rs226684808	in-del	-/TTTT			intron-variant	Arhgap10	Mm_Celera	8:77314481	ACTCTACCTTGTATC[-/TTTT]TTTTTTTTTTTTTAA	78514
rs226688805	in-del	-/TGGCTTGCTCCCCA			intron-variant	Arhgap10	Mm_Celera	8:77282413	AAGAGTGCTGCTTAT[-/TGGCTTGCTCCCCA]TGGCTTGCTCAGGCT	78514
rs226690938	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77447211	TCAGAGATCCACCTG[C/T]TTCTGGCTCCCGAGT	78514
rs226704159	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77324084	AGTCTCCGAGTATTT[-/G]TTTTTGTGTAGCACA	78514
rs226714869	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77377030	CCCATGAATTCACAG[C/T]TTGCTACAATGTTGA	78514
rs226721165	snp	C/G			intron-variant, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77517531	CTATTCCTCCAGCCC[C/G]GTCTTAGGAGCACTG	78514
rs226722154	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77422720	ACAAGGCGGGAGCAG[C/T]AGCTTCGAGGAGAGA	78514
rs226724071	in-del	-/GCCTACATAT			intron-variant	Arhgap10	Mm_Celera	8:77422043	TACGATTTGGACATG[-/GCCTACATAT]GCCCTGTAAAGCCTG	78514
rs226727543	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77472731	TGTACTATATGATAA[C/T]ACATGAATATATATT	78514
rs226762029	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77277124	TTCCTTCCTCCACCA[C/G]CGCTCCAGAGCACAG	78514
rs226768817	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77421389	GGCTGGGAGCCCAGG[A/G]GAAGTCACGGCTTCC	78514
rs226776483	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77378014	GACCTCACCGCTTCC[A/G]GTCACTCAGAGGCAA	78514
rs226793862	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77254099	ACACAGAAGAGCCCA[C/T]ACTTCATACCTGACT	78514
rs226799207	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77354348	TCTCAGCCCCTCTCC[C/T]CCCACCCCACCTCCT	78514
rs226808818	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77294323	ACTATTTTATAATTT[-/A]TAAAAAAATCTACAT	78514
rs226832182	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77373969	GGCAAGACCACATTT[C/T]TGTTGTGGCTAAGCA	78514
rs226839444	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77271871	TGATGTCACGAACTC[C/T]GAGGAGCCTGGGCTA	78514
rs226840539	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77254420	GTAATGGGATCTGAT[A/G]CCTTCTTCTGGTGTT	78514
rs226840782	snp	A/G			intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77492580	CAGCTGCACTTATCC[A/G]CCACACCAAGAATAG	78514
rs226842515	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77278168	GGGATGGTGCTGAGC[A/G]GGGTCCTGCAGTAAC	78514
rs226845034	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77428325	ATTAAATATTACTCA[C/T]GAGAAGTTATAATGT	78514
rs226847975	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77499012	GCCCGCTGCCCGCTG[-/C]CCGCTGCCTCTGCCT	78514
rs226860283	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77491236	GCCCCCTTCTGGTGT[C/G]TTTGAAGACAGCTAC	78514
rs226868501	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77471490	TCAAAAGATGGCCTA[A/G]TCGGCCATCACTGCA	78514
rs226872914	snp	C/T			intron-variant, synonymous-codon	Arhgap10	Mm_Celera	8:77476574	AAAACTGCTGGTCCA[C/T]GGCTTCAGTACTAGG	78514
rs226873823	in-del	-/TAAACAAAAT			intron-variant	Arhgap10	Mm_Celera	8:77260616	TATAAGAAACAAAAA[-/TAAACAAAAT]CTCAAAAAATATTAA	78514
rs226877204	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77352718	TAAGGACAGTTGCTC[C/T]GTGCTGAAAGGGGGT	78514
rs226879924	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77252908	ATTTCACTTAGGAGA[C/T]CCTCAGGTCCAGTCA	78514
rs226885551	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77406135	TCTGGGGCCAGCTTC[A/G]TCTACAGACTGAGTT	78514
rs226896346	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77421504	TGCCTGCGCAATATT[C/T]GAATGGCTAAAATAA	78514
rs226900123	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77441886	CACCCACTTTAGAGA[C/T]ACTGGTTGCTAGAGC	78514
rs226913614	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77359358	AAAACTAGCAAACTA[G/T]CTTTCTTTGTCGGAA	78514
rs226916707	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77443118	TGCTGGGATTAAAGG[C/T]GTGGCCCACTACGCC	78514
rs226921271	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77516139	TACACATCCACTTCC[C/T]AGTCCATGGATGTCC	78514
rs226922216	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77464436	CAGTAATAGAACCTT[C/T]TTGTGCAAGAAGGAC	78514
rs226931162	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77328292	TGACTCTTACATCTG[A/C]GGTTTGTCCTTCCAG	78514
rs226935737	in-del	-/TA			intron-variant	Arhgap10	Mm_Celera	8:77491284	AAATAAATAAATCTT[-/TA]AAAAAAAAAATTAAA	78514
rs226944961	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77447785	ATTAAGCTGGGGCTA[C/G]CTTATCATTCAGAGG	78514
rs226951110	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77370436	CTGAAGTAGAGAAAA[-/G]AGAGAGAGAAAGTCT	78514
rs226953355	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77382274	ACAGAAGGGACATGT[A/T]TGCACACAGAAAGGA	78514
rs226958011	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77401010	CTAAATCCGACTCGA[A/G]TCTCCGCCAATGTTC	78514
rs226967508	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77427840	GTCTTGCTCCTGGAA[C/T]CTCGGCTCACACAAT	78514
rs226970883	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77253602	GTTTCAGCTCTGAAA[C/G]TGCAACACAGGCCCC	78514
rs226990250	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77401483	GCTATCAATGTATGA[C/G]TACCTACGAAATCAC	78514
rs227007656	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77447405	CGAGAAATCTCCATC[A/G]GAGTCCAAGACCACA	78514
rs227007861	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77453108	TTCTAGAATGACATT[A/T]TTAAATAAATTCTTC	78514
rs227015724	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77382014	AGGGTATTAGAGTAA[A/G]TTGCGTGTGTACATA	78514
rs227016499	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77417696	AAGAGAGAGAGAGAA[C/T]AAGATGAATAGCCGA	78514
rs227016619	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77353628	ACTTCATTCAGAGGT[C/T]GCAGAGGAGCAGGAC	78514
rs227022484	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77454503	CTAGCAGTCACAGTA[A/C]ACTAAGATACATACT	78514
rs227024000	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77448175	CGCATGCGCGCGCGC[A/G]CACACACACACACAC	78514
rs227027191	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77359949	GATCCTGTAAACTCA[C/T]GTGTGCATCCTAACA	78514
rs227066174	in-del	-/GGGGGGGGGGGTGTT			intron-variant	Arhgap10	GRCm38.p3	8:77413921	TCTACGGGGGGGGGG[-/GGGGGGGGGGGTGTT]ATAAAAGGTGTTCGA	78514
rs227075922	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77307778	AGAAAGAAATTAAAG[A/T]GTTTAGAATTTAGTG	78514
rs227077459	in-del	-/A			intron-variant	Arhgap10	GRCm38.p3	8:77260415	TAGAATTTAAAGTGT[-/A]AAAAAAATGGTTCCG	78514
rs227089828	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77375951	GTGTCAACACACAAA[A/G]TCAAGACCACTAACC	78514
rs227108826	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77447993	ATAATAGTGCCACTC[C/T]CTATGGGCCAAGCAT	78514
rs227117545	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77471565	CGGTGCTCTTAACCA[C/T]TGAGCCATCTCTCCA	78514
rs227123372	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77489971	TCTTATCAGGTTCTG[C/T]CATAAGTGCCTTAGA	78514
rs227129315	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77253866	CCATCAACTTCCCAG[A/G]GGATGCCAAAAAGCA	78514
rs227130484	snp	C/T			intron-variant, downstream-variant-500B	Arhgap10	Mm_Celera	8:77358166	TTCTCTCTCTCTCTC[C/T]CCACTACGCCCTAGT	78514
rs227131329	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77466650	CCAGCTTGCTCCTCC[A/T]ACACCGCACCACTAA	78514
rs227133588	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77293210	CAAAAATGCCAAGAA[C/G]AACCATTTCCAACCC	78514
rs227139586	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77332018	GGGGACCGGCTCTCC[A/G]CCTCGGGATCTCTAC	78514
rs227141665	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77361123	ATTCACACCTAAAAT[A/G]TGTTTAGAGTGTTCA	78514
rs227141808	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77354023	AGGGGATGGACAGGC[C/T]CAGTACTGATTACAG	78514
rs227156881	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77257883	GCACACAAGGCCCAG[C/T]TTCTCCTAAATAGTA	78514
rs227163313	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77422256	ACTGTCACATGAAGC[A/G]CATGACCACAGTGAG	78514
rs227170790	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77470921	GGCTCTAGGAACTGA[A/G]CCCAGGTCCTCTGGA	78514
rs227178901	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77275800	TGCTGTCCTTGTGTT[A/G]GGCCTGAATGTGCAG	78514
rs227181038	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77332212	GCTGGTGAGCCATTT[G/T]TAAACTGACCTAAAA	78514
rs227186821	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77352039	ATCAAAAGAATACAC[A/C]GGAAGTATTAAAGAA	78514
rs227188932	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77509923	GCAATTAGCCCTCTC[C/T]TCACTGTTTCCTAAT	78514
rs227202302	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77497066	ACCCTGTCTCAGAAA[A/G]AAAAAAAAAAAAAAA	78514
rs227214003	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77326087	ACAATGCCAACCCAT[A/C]ACAGACATGCATTCT	78514
rs227214337	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77475279	TAAGAGCAGCCCAGA[C/T]AGAACATGGCAAGTT	78514
rs227217018	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77444011	GTAATACATAAAGGT[A/G]AAGAGGTTGCCCTGC	78514
rs227226618	in-del	-/TT			intron-variant	Arhgap10	Mm_Celera	8:77365476	ATTTATTTACTTGGG[-/TT]TTTTTTTTTTTTTTG	78514
rs227239298	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77453039	CTGAACCAAGAAGGA[A/G]CAAAGGTCCTTCCTT	78514
rs227242380	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77332939	CAATTGCCAACACTT[A/T]GAAATTATTTTTAAA	78514
rs227261131	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77496496	TTCCTCTTTTCTTTT[C/T]TCCCTGGTCCCCCTC	78514
rs227264434	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77426929	CAGGGTGGTGGGGGC[A/G]GGGGGGGGGGGAGGT	78514
rs227280950	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77337288	AAGCTAGGCCTGGCA[C/T]CGGATCATTTACCAC	78514
rs227285326	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77331192	TTGATCAAAATGCTA[C/T]GTATCATTTAAACTT	78514
rs227293603	in-del	-/CA			intron-variant	Arhgap10	Mm_Celera	8:77418252	GACATGGCTCAGTCC[-/CA]CTGGAGTCCCTCTTT	78514
rs227301957	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77271586	GGTGCCAACACACCC[A/T]GGCTGAAAAGAGGCA	78514
rs227302906	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77333566	TCAGACGAGTGGCTT[C/T]CCTATCCCTCCTGTC	78514
rs227325413	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77433832	GCTTAATGTAAGCCA[A/G]GGCTGCTCTGCGCTC	78514
rs227331896	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77448690	ACCTGTGCACACTGC[C/T]GCATCCCTAGCCCTG	78514
rs227340322	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77331640	ATAAGACAGCACCTA[A/C]TCCTGAGAGCCTGGA	78514
rs227348537	in-del	-/GGCGGGCGGGCG			intron-variant	Arhgap10	Mm_Celera	8:77416633	ACAGACAGACTGGCA[-/GGCGGGCGGGCG]GGCGGGCGGGCAGGC	78514
rs227351918	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77327838	ATGCTTGTTTTCATG[A/C]TCTTTCGTTTTCTTT	78514
rs227382632	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77432698	CAACAGTAGAGACAT[A/G]GGCATGTTCTGTTTA	78514
rs227384246	in-del	-/TTTGTT			intron-variant	Arhgap10	Mm_Celera	8:77477139	AACCTCCTGAAACTG[-/TTTGTT]TTTTTTTTAAGCCAC	78514
rs227393264	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77305464	CAATAATAAATGTAA[C/T]TGTGTTATAAAAACT	78514
rs227409574	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77280480	GTCTGTCTACTGGGC[-/A]AAAAATCACTGTAAA	78514
rs227424570	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77421164	GCACTTGGGAAGCTA[C/T]GGCAGGAGGACATGT	78514
rs227431438	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77459746	GGGCAAGCCTCTCTG[A/G]AATGCTCTCACAGAT	78514
rs227432472	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77375164	GCGATGGAAAATTTC[A/G]ACTAACATAAATTAG	78514
rs227433577	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77452793	CTTGGTGGTTAGGAG[C/T]ACTGCCTGTTCTTCC	78514
rs227435568	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77446461	AACTGCGCTGGCCTT[G/T]CAACCTTTATTAATT	78514
rs227440575	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77313181	TTGATGCTTGGAACT[A/G]ATGTTAGTGAACTGG	78514
rs227475099	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77375578	AGTCCCAGGAACTCA[A/G]GGGAGCCGTTCCCCT	78514
rs227495371	in-del	-/TGT			intron-variant	Arhgap10	Mm_Celera	8:77384018	TCAGCACCTCCCTGC[-/TGT]TGCTGCTGCTGCTGC	78514
rs227497399	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77306446	AAAGGACAATAAATA[C/T]CTTCAATAAAATTAT	78514
rs227513503	in-del	-/CCCTGCT			intron-variant	Arhgap10	Mm_Celera	8:77498979	TCTCTCTGCCTCGCC[-/CCCTGCT]CCCTGCCCCCTGCCC	78514
rs227513938	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77420620	GGATCCACAGCAACG[A/C]GTGTCCTGCTACTCA	78514
rs227515873	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77404387	AGAAAGTGAACCAAG[C/T]CCAGACGGAAGCAAA	78514
rs227519574	in-del	-/TG			intron-variant	Arhgap10	Mm_Celera	8:77254203	TCAGAGAACAGACCT[-/TG]TGGTAGTGCATGGCA	78514
rs227521051	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77297359	ACTCTTCCAAAGGAT[C/T]CAGGTTCAATTCCCA	78514
rs227536929	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77275097	CTTTTGGGATAGCAT[C/T]GGAAATGTAAATGAA	78514
rs227538198	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77356598	TCCAAACCACAGTCA[C/T]GACTCAGGGCAAGCT	78514
rs227540200	in-del	-/TAG			intron-variant	Arhgap10	Mm_Celera	8:77511637	GTTTTATTTTTTTTT[-/TAG]GACAGAGTCTCGGCC	78514
rs227559818	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77312368	CTTGAATTCTACCAA[A/C]AAGGCAGATGCCTCT	78514
rs227575913	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77426698	TCGAGTTGAGAGGTA[A/G]TGATATGTCAACCTT	78514
rs227576647	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77496681	CTTTGGCAAAGACAG[A/G]GGGATCTGTAGGCAC	78514
rs227580683	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77427401	TATTAAAAGCATGTC[C/T]ATCAACGTCCCGGTC	78514
rs227583162	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77256131	AACCACTGTGGGATG[A/G]GCTTAGCCAGCTGCA	78514
rs227594415	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77270710	GACCAACCACAGTCC[A/G]GTGCATGGCAGCACA	78514
rs227616443	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77513475	TCGTTCTTCCAAATC[G/T]CGGTACAGTGTGTAA	78514
rs227631766	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77273860	CCCCAAGATTATGAA[C/T]GGAAAACCTTGCTGT	78514
rs227633222	in-del	-/ACAG			intron-variant	Arhgap10	Mm_Celera	8:77448198	CACACACAAACATAC[-/ACAG]TCCTTATATAATATA	78514
rs227640502	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77421782	GTTGGCTCACGTGAC[G/T]CTCATGAGGCATCAC	78514
rs227646928	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77447747	GACGCATCGTGGCCA[C/T]GGCTACTCTTATGAA	78514
rs227649322	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77413223	CAGAAAGGTGCTGGT[A/G]ACATAGTCCCTCCTG	78514
rs227649668	in-del	-/CT			intron-variant	Arhgap10	Mm_Celera	8:77367849	CAGCAATGTTAATCA[-/CT]CTGAGCTTGTAATTA	78514
rs227652469	snp	A/C			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493737	AGACAATGAAGATTT[A/C]TATCTGCCGAACAGA	78514
rs227653695	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77381932	TTGTATCCCATAAAG[-/T]TTTTCAACCTCAGAA	78514
rs227655508	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77405166	CAGCCCCAGCTCGTG[A/G]GATTCATAATCTAAC	78514
rs227665140	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77489213	ATATATATACACACA[C/G]AGACATTCACATACA	78514
rs227681916	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77290783	AAGGGGTCGAGACTC[-/A]ATGGGTTGAGAAGCA	78514
rs227682967	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77469130	CTTCCTCAGCTACTT[A/C]CTCAGCAACAGTCTC	78514
rs227683396	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77271346	TGTGAATTCCTGTCC[C/T]GACTTCCTTTGGTGA	78514
rs227697080	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77455703	TGGAAGAACACCCAG[A/C]CTATTGTGGGTAGTG	78514
rs227698719	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77293164	AGTTGGTACCCAGAG[-/C]CCACTGCTGCAATAT	78514
rs227700665	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77319118	AAACTTTATATGCCC[C/T]AGTACAGGGGAACGC	78514
rs227702646	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77314231	CGTGTAGGAATGCTG[C/T]TAAATTATATCCTTT	78514
rs227702867	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77516193	TTTCTCCACATTTAC[C/T]GACTCTCCCTCTGTT	78514
rs227705100	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77499807	GCTTTATGTCTAATA[G/T]AGTCCCTCACCAGAT	78514
rs227711120	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77405850	GCAACTAAAACTTTT[A/T]AAAACATTTACAGAT	78514
rs227711209	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77513071	GGGGATTAAACCTCA[G/T]GCAGGCTAAGCAAGC	78514
rs227713282	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77374247	ATTCTGCCCACCATC[G/T]TTTATTATCTGATCC	78514
rs227717767	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77499234	AGGGCATGTAATGAA[C/T]TCAAAGCTAACCTGG	78514
rs227722404	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77280842	CAAGTAGGTACGTTA[A/T]CAAGTTCTCACCTAA	78514
rs227728154	snp	A/G			utr-variant-3-prime	Arhgap10	GRCm38.p3	8:77250900	TGCCACGATCAGTAG[A/G]ACCCCCCACGGCCGG	78514
rs227732871	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77380694	AACAAAAAAACAAAA[A/C]AAAAAAAAAACCTCA	78514
rs227738467	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77425048	CTCCTGGCCAGGCGG[G/T]TCACACCAACAGGAA	78514
rs227739626	snp	G/T			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77515558	TCCAACTTGCCAAAA[G/T]GGTGTACACCAACCC	78514
rs227754633	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77336164	GAAACCTAAAACGCT[A/C]TGGTCCTAAGCACTC	78514
rs227755007	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77474689	ACCCAAAGAAGTGAA[A/G]CGGGTAAAGCGCTTC	78514
rs227756952	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77315043	CCTTGGACCAGATTT[C/T]CTGAGTCCAGAATAC	78514
rs227767567	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77404891	CCTGCCTCTGCCTCC[C/T]GAGTGCTGGGATTAA	78514
rs227771558	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77298366	CATAACCATAATATA[G/T]TTTATGAACAAAAAT	78514
rs227773480	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77312426	CAACATCCTGGGCCA[A/G]GACATCCAAAGCACC	78514
rs227774509	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77329845	CCTACATGGGCACTG[A/T]GCACAGATGTGGTAC	78514
rs227776374	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77468028	AAGACCCTCAACGAA[A/G]CAGACCCCAAGTCCC	78514
rs227777905	in-del	-/CACACACACGCGCACGCATC			intron-variant	Arhgap10	Mm_Celera	8:77421042	ACCTGCACACACACA[-/CACACACACGCGCACGCATC]CACACACAGGCGCAC	78514
rs227778706	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77273468	CTCATTAATAGAAGT[A/G]TGCTAAAAATTGATG	78514
rs227784808	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77461210	AGGGAAAAGAAAATA[A/G]AAAGGAAAGACAGAA	78514
rs227794107	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77470489	AATTCTCTGTCCAGG[A/G]GGTTACTAGACAAAT	78514
rs227810207	in-del	-/GTG			intron-variant	Arhgap10	Mm_Celera	8:77320129	AAAGTGTATCCAGGT[-/GTG]GTGGCACACACCTCT	78514
rs227810709	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77379990	CCTGACTGGCACTAG[A/G]GCTAAACCATGATGG	78514
rs227812183	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77381641	CATGACACAGAGGTA[G/T]AAAATCCGCAAACAA	78514
rs227813968	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77375265	GCAGACCAAAGCATC[A/G]GCCTTGCCTTGAAGC	78514
rs227816145	in-del	-/AGACT			intron-variant	Arhgap10	Mm_Celera	8:77289664	ACACCCTATCACAGG[-/AGACT]ACACACTGCTCTTTC	78514
rs227816774	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77374829	AGGTTCACATGCAGA[C/T]AGACAGTTGTCCCTA	78514
rs227818712	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77280112	GACCAGCCTGCTCCT[A/G]ACTCCCTCCAACCAG	78514
rs227824129	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77282758	CTACCGCAGCCAGTA[A/G]CTTAGGCTAACTGTA	78514
rs227830993	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77303958	CCCGAGAGAGTTGCA[C/T]GGCTAAGCACTGCAG	78514
rs227849109	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77280903	AGCTTTTACCTCTTA[C/T]AAGATTAATTTATAA	78514
rs227852008	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77274586	TGCAATCAGTCCAGG[G/T]TGGAATCAAGAAAAG	78514
rs227852821	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77469819	TTGGGTTCAGGCTAC[C/T]GAAGTTGAATATGAT	78514
rs227866468	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77375604	CCCCTTTGTAAGCTG[C/T]CATGAGGAGAAAGAA	78514
rs227867691	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77274023	AGAGAAGGTGCAGTC[A/C]GTAAAGACAAGGTAA	78514
rs227904102	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77475410	GAACTAAATGATCAA[A/C]GGTGGGGGAAAACCG	78514
rs227922214	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77273547	GGACTGTTAAGAGAG[C/T]AGATGCCTGAGAGGA	78514
rs227927565	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77275370	GAGTCTCTCACTGGA[C/T]GATTACGCCTAGCTG	78514
rs227948862	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494091	GGGCTAAAATGCCTA[C/T]ATTCTATGATAAACA	78514
rs227952677	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77262216	AAGCCTGTCCCTTAG[G/T]ACTGTTTGTTGCAGC	78514
rs227952837	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77254519	GGGGAAGGGAAGGGG[A/G]AAGGGGAAAGGGGAA	78514
rs227953171	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77356075	CGCCTATATTATATA[C/T]AGGATCAAATAATTC	78514
rs227956441	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77479538	GTGTGCACAGCACTG[A/G]GTCCAAGGAGGTCAG	78514
rs227956515	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77256212	GACAGTACAATGCAA[A/G]GAATCACACATGTAA	78514
rs227964480	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77357095	TATCATCTAAACCCT[A/G]TGAACACAGGCTGAG	78514
rs227982636	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77254780	AAGAAAACAGCCTTG[C/G]GTCTCAGGGATGTTA	78514
rs227994698	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77451497	TTCTCCAAAAGAGCT[A/C]CAGACCCATCGCCTC	78514
rs228003228	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77386194	TCACTATCTAAAGTA[C/T]TTCTAAAGGCTCTGG	78514
rs228008201	in-del	-/TTTCTT			intron-variant	Arhgap10	Mm_Celera	8:77480576	CACCACACCTGGCTC[-/TTTCTT]TTTTTTTTTTTAAAG	78514
rs228012017	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77311756	CTGCAACCACAGGCA[A/G]CCGGCACGCTCCTCA	78514
rs228012440	snp	C/G			utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250805	TCCATCCCCTCCCCA[C/G]CCTGGAGTACCCATG	78514
rs228040739	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77450423	CTTTAGGGTAACATA[C/T]ATGCAAGTCAAAGGC	78514
rs228041058	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77255442	AGTAATCAAAGCTCA[A/G]GCTTCAGAAGTCCTC	78514
rs228041901	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77256934	TGCAAAGCACAGGGA[C/T]GGTGCCAGAGAGGGA	78514
rs228042949	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77252017	TTGTTTTCCCCGTTG[C/T]GAGAAGTTCTGTGAA	78514
rs228060211	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77296102	GAAGCCAGTACTCTG[A/C]TAGCAGCCTTCAGAG	78514
rs228065554	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77501502	AGCGGATGAAGAAGA[C/T]GAATCCAGATGACCA	78514
rs228067646	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77482433	AAGGGGGAAGAGGGA[-/G]GGGGGAGGGGAGAGG	78514
rs228071488	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77252348	CTTGTACAATAAATG[A/T]TTTAAGGTGTGCTTT	78514
rs228079447	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77419889	AGGGCCTCCAAAGGG[C/T]AGAATTCCTGGAGCC	78514
rs228099331	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77500848	ACATACTAAACACTA[C/T]CATTCATACCAATCC	78514
rs228112456	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77251541	CCCACTCCCACACTG[A/G]TTAGGGAGTTCCTGA	78514
rs228117979	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77456863	CTCAGCTATTAAAAA[C/G]AATGAATTTATGAAA	78514
rs228118257	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77451016	GTGCTCCACTAAGAA[C/T]TCAAAAAGCCACAGC	78514
rs228121476	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77455629	CGTCAATTAAGAAAC[A/G]CCTCTGTAAGATAGT	78514
rs228121659	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77362423	CAAGTAAATATTGCC[C/T]TCTTCTAAAAACATA	78514
rs228148414	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77379411	CGCCTCTGCCAACTT[A/G]GTCCCCTTACTTAGG	78514
rs228149885	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77385314	TGGCTCCTTATGCCT[G/T]CTCAGGCTGTAACAT	78514
rs228159690	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77456285	AAAACAAAATTCTTC[C/T]AGGACTATGGACTGG	78514
rs228162815	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77362904	CGGGCAATCTGACTC[C/T]TATTACCAGTTACCC	78514
rs228180418	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77379858	TTCTGCTCTGTCTAC[C/T]ATGACTGGTTTACAG	78514
rs228223869	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77341400	GGCCTCCGACGCAGA[A/G]GAACTTCGTCTCCTC	78514
rs228226955	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77474746	CAGTGGAGTTCAACT[A/G]CAGATGTGAGTAAAA	78514
rs228228242	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77367703	ATCCTAAGGATTTTA[C/G]GCCCCCCCTCCCCCC	78514
rs228230756	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77415481	ATGCATATACAATGG[-/A]AGCCACTATTGATAT	78514
rs228233906	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77441167	GGAGGCCGAGATGGT[-/A]ACATGCTATGCTCAA	78514
rs228262256	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77335618	GTGGTGACTAGCAGA[A/G]CTAGAAAAGAGCAAA	78514
rs228265241	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77273197	TAAATGTAAACAAAA[A/G]GACAAACAAGAGGCA	78514
rs228266001	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77373359	GAACCTTGGATTCAG[-/A]AAAATCTAAAAACAA	78514
rs228284996	in-del	-/AAAC			intron-variant	Arhgap10	Mm_Celera	8:77290239	CAAACAAAAAAAAAA[-/AAAC]CAACAACAACCAAAC	78514
rs228289639	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77474053	TTAGATCTCTGTGCC[C/T]CAAGGCCTTTTATGG	78514
rs228295852	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77361308	CTGCCTCGAAGCCGA[A/G]GTGTGTGCCCCATGC	78514
rs228296840	in-del	-/ACGC			intron-variant	Arhgap10	Mm_Celera	8:77374715	GAGGCTCACATGCAG[-/ACGC]ACAATTGTCCCTACT	78514
rs228309566	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77368392	AGTGCAGAGCACACA[A/G]AGCGCATGCTAACCA	78514
rs228315086	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77451515	GACCCATCGCCTCCA[C/T]TTTCCATGGCAGGTC	78514
rs228320949	in-del	-/ATATA			intron-variant	Arhgap10	Mm_Celera	8:77472589	AAAAGATATATGTGT[-/ATATA]ATATAACAAATATAA	78514
rs228323224	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77357230	TAGTAATATATCTGC[-/A]AAAAACTCTTTTTAG	78514
rs228333088	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77330302	GGTTTTCTTTATGGA[A/T]GTGGGAGGAAAGAAT	78514
rs228358441	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77310703	AACATGCCATGCCAC[C/T]GAGCAGAAAGCCCAA	78514
rs228373342	in-del	-/TCTAAGT			intron-variant	Arhgap10	Mm_Celera	8:77375075	ACGTGGCCAGGAACG[-/TCTAAGT]ATAAAGTAAGCTGAG	78514
rs228373397	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77448699	CACTGCCGCATCCCT[A/G]GCCCTGTGCACACTG	78514
rs228374760	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77253040	TCCATCTTTGGGCTA[-/T]TTTTTGAGTACTGCT	78514
rs228375414	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77479914	CTCCCTAATATGGCT[A/G]AATCTGATACCGAAT	78514
rs228375481	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77473291	TCACGCACGGTTATT[A/T]TTTTTTTTCCAAAAA	78514
rs228378390	in-del	-/CTT			intron-variant	Arhgap10	Mm_Celera	8:77513453	TTACAGAGAACTGAA[-/CTT]CTTCTCGTTCTTCCA	78514
rs228383584	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77361667	AGCACAGTTTCTCCA[G/T]GTTTCCCCTGCTCTG	78514
rs228399899	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77424453	GACAGGGCAGAGCCC[C/T]ACACCTCAAGCACTG	78514
rs228406820	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77261193	CTTCATCATCATCAC[C/T]GCCCTCAGCTCAAAC	78514
rs228409485	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77412558	GAAGACAAGGTCTCC[A/T]TTAAACTCAGAGCCT	78514
rs228413192	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77275650	AACACAACCCTTCCC[-/A]GCTTGCTTCCTCTGC	78514
rs228415004	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77403111	TAAACAGATAAACTG[C/T]GGGGATAAAAGGCAT	78514
rs228432517	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77408651	ACCAGTTTGTCGTGA[C/T]GGACTTAGATCTTAG	78514
rs228444186	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77467625	TCTTCAAGGGATTCA[A/C]CTTCCAAAAGCTGCT	78514
rs228446947	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77498915	TCTATAGACCAACCA[A/G]GCTGGCCTTGAACTC	78514
rs228452834	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77414558	TCCAGAGGGTTATTT[-/A]AAACAGAAACTAAGA	78514
rs228459718	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77355034	GACCAAGGGAGGGAC[C/T]GTGAGGAGGACACTT	78514
rs228463412	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77339313	AGGTCAACCCAAACC[A/G]TTCCATCACACCGAG	78514
rs228468649	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77454695	AACTGTGAGAACTGC[A/G]TATGTCCAGATTATC	78514
rs228470613	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77362408	TATCTAAACAGGTCT[C/G]AAGTAAATATTGCCT	78514
rs228475695	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77431331	TGCATGGCTCTGTTA[A/G]AAGAGACCACTTCTG	78514
rs228477658	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77318066	CAGTCTCCTGCCATT[-/C]CCCCCACCCCACCCC	78514
rs228485242	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77407666	GCAGAGGCAGAAGAC[A/G]ATGGGAGCTCAGAGA	78514
rs228491650	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77498052	GGAAACCAAAATGAA[G/T]AAAGCGGAGAAAGCA	78514
rs228496898	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77384070	TGAAGAGCGAGCGCA[C/T]GCTTTAGCTGCAAGG	78514
rs228508048	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77430821	GAGAGGCAGGCACTG[C/T]GGATGAGGTCAGCAC	78514
rs228510479	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77430844	GTCAGCACACAGGGA[A/G]AGGAGAGGAGAGGAG	78514
rs228512256	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77310392	CAGTGCATTGGCTCC[A/G]CTAGCTCCTCACATC	78514
rs228512478	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77316940	TCAATAGAACTTACT[A/G]ACATGTAAGTAAAAA	78514
rs228521724	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77408136	ACCCCTTATCTATCT[C/T]TCTGAGTAGGAGAGA	78514
rs228533587	snp	A/G			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519760	GTTCTTTTATAAATC[A/G]CCTTGGTCAGTGTGT	78514
rs228536510	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77403979	TTTTGTGTGGACATA[A/T]GTGCCACTCCATTCA	78514
rs228542473	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77438346	ATCCGTTACAGGATG[G/T]CATTTCTCTGGGGGA	78514
rs228546392	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77317328	GAAGTAGCTGGCGTC[A/G]CCTCAAAGAATTTTC	78514
rs228546680	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77333733	CCTAAGACTCTTGAA[A/G]TAATATACACAATCC	78514
rs228553127	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77339781	CACCCTTACTCCCAA[C/T]GGGAAGGAACCTTAC	78514
rs228556839	in-del	-/GGGAGG			intron-variant	Arhgap10	Mm_Celera	8:77462337	CATGTCAGCAATGGA[-/GGGAGG]GGGACTCCCATGAAA	78514
rs228558979	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77309846	GACACTTTTCTCTTC[A/G]TGTTTATGATGTGGG	78514
rs228559972	in-del	-/TTTT			intron-variant	Arhgap10	GRCm38.p3	8:77327867	TTATATCTTCCAGGG[-/TTTT]TTTTTTTTTTTAATT	78514
rs228561210	snp	C/G/T			intron-variant	Arhgap10	Mm_Celera	8:77472677	ATATGTTATTTATGT[C/G/T]TATATATTTGCATGC	78514
rs228574689	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77286350	CTAATATCACATAAA[A/G]TATTTTTGAAGGAAT	78514
rs228586473	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77383990	ATGTGCTGTGTGTAA[A/T]AAGCTCAGCACCTCA	78514
rs228589709	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77430148	TATTTCAAGCCTTGT[A/G]TTTAAATGTTTGCGT	78514
rs228595205	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77445878	TTGGGATATTCAGCA[A/G]GAGATAGATTAACTA	78514
rs228595218	in-del	-/ACACACACACACACAC			intron-variant	Arhgap10	GRCm38.p3	8:77469320	TTCTGGTAATGGGAG[-/ACACACACACACACAC]ACACACACACACACA	78514
rs228608398	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77436465	CCCACCCTGGAGATC[A/G]AAGGCTGAGTTCTGA	78514
rs228612304	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77384427	CCATGAGCAAGAGCA[A/G]CCTGCTATTCTCAAC	78514
rs228626844	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77278504	GAAACAGTACTAACA[G/T]GGCCTTGATTTTCCT	78514
rs228628477	snp	C/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77287055	TTTATCTTAATGTAC[C/G/T]CACATAACATGGATT	78514
rs228631465	in-del	-/CATCTCAGAAAAA			intron-variant	Arhgap10	Mm_Celera	8:77278693	CAACTCTCAGAAAAC[-/CATCTCAGAAAAA]CAACAATTCCTCCCA	78514
rs228631488	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77411505	ACGCACACACGTACA[C/T]ACATACACATGCACA	78514
rs228631583	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77334191	AACAATGAAGGTAAA[A/G]TCTGTAGAAGAAAGA	78514
rs228640641	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77478071	GTCCAGATGTTTTAG[A/T]GATATCTATAGCAAA	78514
rs228646539	snp	A/G			upstream-variant-2KB, downstream-variant-500B	Arhgap10, 0610038B21Rik	Mm_Celera	8:77518594	AGAGGCGATCTGCTA[A/G]AAATAGCCCGCCGAA	78514
rs228664271	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77279129	ATCCTAGAATATTGC[C/T]TGTTTTTACTTTTAG	78514
rs228678281	snp	A/G			synonymous-codon, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77450844	TATGCACCGTTCATC[A/G]TCAGTCTCAGCATCG	78514
rs228679347	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77436108	TGACATACATCCTCC[A/G]ACAAGGCCACGCCTC	78514
rs228686867	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77379266	AAACGCAGCAAGGAT[A/G]TGTCACAAATGTCTC	78514
rs228695618	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77478738	CAGTCAAAGCTGTAA[A/T]GACTGGCTCCCTAGG	78514
rs228702858	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77407129	AACACAACATGTATA[C/T]GATGCACAGACATCT	78514
rs228703288	snp	A/C			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484147	TCCTAAATCGAATCC[A/C]CTGCGCTCCTCAAGG	78514
rs228715681	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77259668	AAAGCTAATCCCGGG[C/T]TGGTGAGATGGCTCA	78514
rs228721451	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77455275	TCACATAACGCAGAA[C/G]CACCTGCCAGAGGTG	78514
rs228731298	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77360554	GAACTACAATGGTGA[C/G]TGACACCGGTTGGCT	78514
rs228736169	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77334824	AGAGGAGAATAAGTT[A/T]CTTTGACAGGGAAGG	78514
rs228743194	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77279853	AATTGGCTTCTCGAC[A/G]GGGCTCTGTCTACAG	78514
rs228750798	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77272630	CTCTCCCCTCTTTTT[C/T]CCCCTCTTTTTTTGC	78514
rs228764254	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77396081	GGGGTGCAGGAACCC[A/G]TACAAGTGTACTTCT	78514
rs228768167	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77499537	AGATCTTGTCTCCGG[-/C]CCCTCAGCTTCCTTT	78514
rs228770411	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77498522	GTCTGTACCTTCAAC[G/T]GGCTTGTCTCTGAGA	78514
rs228776724	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77316255	TGAAAAACACCTTCA[A/G]CTCTGATTTACAAGT	78514
rs228779097	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77471657	CCCTTCCCCCCCCCC[C/T]TTTTTTAATAATCAC	78514
rs228798358	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77260218	CTTAAACACTGAGCA[C/T]GTGACCTGCGGCCGA	78514
rs228800312	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77253662	CGTCTCCTTCCCAAC[C/T]CTTAATGAAAACACC	78514
rs228810451	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77254686	CATAAACTGGTTTGT[C/T]CTTGCCTACATTATA	78514
rs228814724	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77323436	GTTTTATCAACTCCC[A/G]TGGCACCTACAGGAA	78514
rs228816854	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77402475	ATACATAAAATAAAT[-/A]AAAAAATCTTTTTTT	78514
rs228825485	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77449980	TCTAGGCAGTGTTCA[C/T]TCTGAAGTATCAAGA	78514
rs228826547	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77396384	AGTGGTAAGAAACCT[C/T]TTGCTCCATGGATCT	78514
rs228827267	snp	A/C/G/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77504287	TGGGGGGGGGGGGGG[A/C/G/T]GCAAAACAAAACCTT	78514
rs228831473	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77361249	GCACACAACCAAAGA[G/T]CTGGCACTTTCTTAC	78514
rs228851724	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77491669	AAGGGGTATGGCCAG[A/C]GCTCCCGTGGCCACA	78514
rs228855733	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77316920	AATGGCTGCAAATTT[C/T]CTCCTCAATAGAACT	78514
rs228859072	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77436034	AGGCACTTGGGAGCA[A/G]GCTCTCTTCCTCACT	78514
rs228859792	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77497133	GTGTGATTTTTTTTA[-/T]ATTTATTTAATGTAT	78514
rs228863463	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77382854	TTTCCCTTACAAAAA[A/G]AAGGAAAGAATTAAG	78514
rs228870839	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77429782	CCACTTCTGCAGGGC[A/G]TGCTTACTGTTCTCC	78514
rs228879119	in-del	-/GG			intron-variant	Arhgap10	Mm_Celera	8:77374644	ATGTTACTCTTGGTG[-/GG]GCTCTTGGTAACTGA	78514
rs228882711	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503699	GACGGACGTCAATGG[C/T]GCTGGCACTAGAATT	78514
rs228882787	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77383550	GAATATGCATCACTA[C/T]GCTGAAAGTGAATTT	78514
rs228888028	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77477365	AGCTACATAGTAAAA[C/T]CCAAGAACAAAGAAG	78514
rs228894024	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77410288	ACAAAGTGTAAGGTA[A/C]ATAGACAGAAACCAG	78514
rs228894272	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77455141	AAACGACTTGAGGAA[A/G]AAGTTTATAGTTCAT	78514
rs228900712	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77354481	GCAGAGGAAGGGAAA[C/G]CATCCATTTTCACAG	78514
rs228906208	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77338560	TCCTCCCCATTGCCT[A/G]ACTCCTAGCATCCTT	78514
rs228911339	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77309651	TGATATTAACGATTC[A/G]CACATTTCTCCAGGA	78514
rs228914580	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77459989	CCATACCCCATTAGG[A/T]AAGGTCAAAGGGAGA	78514
rs228915123	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77453331	CATGTGACCGCATCA[A/C]ACTGCATTCCTTTAA	78514
rs228937813	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77320750	CAAGTTCCCACCTAC[A/G]GGATCTGTAAGAAAA	78514
rs228947038	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77377289	CTCAAAATTAGGTGT[C/T]ATGTGTGCCCATCAA	78514
rs228953133	in-del	-/A			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77503972	GAACCCTCATGAGCC[-/A]CCCCCCCCCTCCAGC	78514
rs228953483	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77254465	CAGTGTACTCACATA[C/T]ATAAAATAAATAATA	78514
rs228953957	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77410761	CTTCTATGTGAACAG[C/G]GGTGGTCAACGAGTC	78514
rs228967319	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77459430	GAGACAGCCATTCAG[A/G]CGCACTGGCTTCACC	78514
rs228980141	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77366029	CTCAGAGAGTTACAG[A/C]TTTCTCCGTGCTTGC	78514
rs228992890	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77321176	CAGATAAAGGAAACC[C/T]GCCTTCTTTTAGTTG	78514
rs229004573	snp	A/G			intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77502167	CCGAGAACGCCTCCT[A/G]CTGAAGAAGCAGCAC	78514
rs229011386	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77332986	TAAGATAATAACATA[C/T]GCTGAGCTCTCAGTT	78514
rs229018478	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77277407	TTCAGCCCGGGAGCG[C/T]GTGGACACTTTGGAA	78514
rs229026051	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77473239	GGATTTATTCTGCAG[C/G]GCCCACCCCAGCACC	78514
rs229029641	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77359736	CGTAGTAAAGGAGAA[C/T]CCTCTGGGCATGCTG	78514
rs229040823	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77333629	ACAAAAAAGGCAGCG[C/T]TGACAAAAACTTCCA	78514
rs229053852	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77315569	CTGTACCCTTCATTC[A/G]TCAATGCCAAACTCA	78514
rs229067782	in-del	-/TCA			intron-variant	Arhgap10	Mm_Celera	8:77477941	GGTTCAGTGAGAATG[-/TCA]TCGACTGCGAGAAGC	78514
rs229073306	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77278319	GGCACATGCACAAAA[A/G]AGCTTCCCAAAGCAG	78514
rs229079765	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77477477	TCAAGGACATCTCAG[G/T]GTTTCAGGTACTAAA	78514
rs229082837	snp	C/G			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519566	GAAAAGGTTTGCCTG[C/G]AGGTTGGCTTTCAGG	78514
rs229092035	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77433047	GAACCTCGGAACTGG[-/C]CCCCGCAGCTCTCCA	78514
rs229099446	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77284022	ACTGTGCAGCTGCTG[C/T]GCTGAAGGGGTTGAT	78514
rs229114903	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77272285	TAAGCATTAGTTCTG[A/G]AAGGGACCTTCAAAA	78514
rs229119866	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77382223	CATGTATGCACTCAG[A/G]AGGGACATATACACA	78514
rs229130905	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77337886	TACTTCAGAATGCTC[C/G]CTGCCCCCAGATCTT	78514
rs229142159	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503686	GCCTCACGGTTCTGA[C/T]GGACGTCAATGGCGC	78514
rs229168801	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77315115	CATCCATCTGATGTC[A/C]TCCACAGTGATGTGC	78514
rs229172799	in-del	-/CTCT			intron-variant	Arhgap10	Mm_Celera	8:77324318	AAAAGGTCACACACA[-/CTCT]CTCTCACTAACACTT	78514
rs229181570	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77284894	AGAAAAGACGAGAAG[A/T]CAATGATTTAGAGAT	78514
rs229184994	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77411935	TTCTCCCACAATCCT[A/C]TACTTCCCAGCTGGT	78514
rs229205203	in-del	-/TCTGACT			intron-variant	Arhgap10	Mm_Celera	8:77284668	AGTCCTAACTGGGGC[-/TCTGACT]TCTGACTCACTTCCT	78514
rs229210569	in-del	-/CAGGCAACACTC			intron-variant	Arhgap10	Mm_Celera	8:77462544	AAGTCATGGGCCCCA[-/CAGGCAACACTC]CCTGTACTGATTGCC	78514
rs229211068	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77453931	AGGACTGCCATTGGG[G/T]AAAGCCTTCCTCATA	78514
rs229215663	in-del	-/AACGAGC			intron-variant	Arhgap10	Mm_Celera	8:77417033	GTCATTTATCACAGT[-/AACGAGC]ACAGGGAAAGGAGTC	78514
rs229221528	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77258363	CAGAAGCCATACTCG[A/G]CTAGATCTGAGCCAA	78514
rs229229335	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77305566	ACACGTGCGAACACA[G/T]CTAAGACCACCTCTT	78514
rs229248731	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77416461	AGGGAGGGGCAAAGC[A/G]GGGGTGGGGGAGGAT	78514
rs229256566	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77264924	TGCTAACAGGTTCTC[A/C]TATCAGAGGAGCACA	78514
rs229256600	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77257262	GGGCCACAGCCAGTG[G/T]CTGGCACTCTATGTG	78514
rs229263066	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77407552	ACAGTCCCACTAACA[A/G]CCAAGGTGAGGAAGG	78514
rs229267971	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77477993	GCTCACGGGCCTCAC[A/G]GCCTCACAGGCCTGC	78514
rs229282673	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77253383	TGCTCCCCTCTCCAG[C/T]GCTGGAATGGTGTGA	78514
rs229291281	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77253608	GCTCTGAAAGTGCAA[C/T]ACAGGCCCCATGCAA	78514
rs229305927	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77314154	CTCAGTGTACTAGCA[G/T]CAGTGCAAAGACTGT	78514
rs229333651	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77257806	ACACCTGCAGTTCCA[C/T]GGCACTCTGGAAGGA	78514
rs229343146	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77428681	CACCATCAGATCTCG[A/G]AATAAAACAAAGGCA	78514
rs229360362	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77388330	TGCAAGCATTCAATA[C/T]ACTTGTCAAAAAAAA	78514
rs229367716	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77415040	TTGGCATTATTCATT[G/T]CGGTAAGATTCCTCC	78514
rs229372035	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77491309	TTAAATAAACAAAGA[-/T]TTAAAAAAAAAAAAA	78514
rs229380789	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77344042	TGAGAGTGAATCCTC[A/G]TGACATAGAAATGTG	78514
rs229380863	in-del	-/CCAGTCA			intron-variant	Arhgap10	Mm_Celera	8:77264048	CTAGGAATGGCCATC[-/CCAGTCA]CCTTTGTGTAGTTCA	78514
rs229392297	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77458576	AGTGACAGGCATAAA[C/G]GCTTACAGTGGAGGA	78514
rs229405155	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77501418	ACTGAGAGAAGCCCC[A/G]GGTGAAGGCTCTGAG	78514
rs229409210	in-del	-/AGGCTGTG			intron-variant	Arhgap10	Mm_Celera	8:77325280	GGCCCTTAGGTCCTC[-/AGGCTGTG]AGTAAAAATATCGGT	78514
rs229415156	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77388915	ATTATTGTACAGCCA[C/G]CCCAATGATTCACCT	78514
rs229418380	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77381887	AAGAATTAGTTCTCC[A/G]ACTGCTGATTCTTCC	78514
rs229420120	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77414491	GGCGCCCTGGTTCCT[C/T]CCTCCTAGGGATGGG	78514
rs229435067	in-del	-/TA			intron-variant	Arhgap10	Mm_Celera	8:77350676	TTTCAACAGTTTAAC[-/TA]TATAAAACAGATCCG	78514
rs229437182	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77275450	CCTAGCTTTTTTATG[C/T]GGGTTCTGGGGACTG	78514
rs229444215	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77339257	TGTCTCCACGAGAAT[C/T]AATGAAATACTTGAG	78514
rs229460059	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77370298	TACAGGATCAAGCTC[A/G]CATACAGAGCTCTAC	78514
rs229469972	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77435133	CAGGAGCAGACCATG[A/T]CAGTCACAACATCCG	78514
rs229471647	in-del	-/AG			intron-variant	Arhgap10	Mm_Celera	8:77383769	CTGAAGATAAAGTAA[-/AG]AGAGAGAAACGCACA	78514
rs229476033	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77378125	ACATTCATTCAAACA[C/G]CAGCACCTTTATTCC	78514
rs229488832	in-del	-/TAGT			intron-variant	Arhgap10	Mm_Celera	8:77454674	TTTTCTATTTCTTGA[-/TAGT]TAAACTGTGAGAACT	78514
rs229488873	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77409447	GAAACACAACAAGGG[A/C]GCATTTTTCTAGTTC	78514
rs229492027	snp	C/T			intron-variant, splice-donor-variant	Arhgap10	Mm_Celera	8:77476539	TTTGATAAAAAGGCA[C/T]CTTTGAAAGAAGACA	78514
rs229516273	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77363701	ATACTCTGCGAGTTG[A/G]AGACTGTCTTGGGAT	78514
rs229524183	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77434675	AATAGAACACTGCAG[C/T]ACCAAATGGGTACCA	78514
rs229526974	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77441786	ATACAAATCTTTCTC[C/T]CTCTGTACCTCCAGG	78514
rs229545365	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77475895	ATATTTAATCTTAAG[A/T]ATAAGAGAAGACACT	78514
rs229545623	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77482576	CTTCAGCATCTTACC[C/T]CTCTGCACTTCACTT	78514
rs229554010	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77365890	GCATTCCAAAACTCA[C/T]CCAACTGTTGAACCA	78514
rs229564715	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77434976	GCTGAAAGGTGTGAA[-/G]GGGTCAGGGGGAGCA	78514
rs229567487	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77410259	CTGCTTTAAGGTTTT[A/T]TGTTTGTTTCTGGAC	78514
rs229575884	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77264476	CGGTTCCCTTCTCAC[A/G]GAAAGAGACGAGGAG	78514
rs229583680	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77441114	TAGATGAGGATCTGA[C/T]CCCAGGAAATGAAGG	78514
rs229590097	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77406225	GAAAAAGTATAAAAG[A/C]AGTAACATATGACCT	78514
rs229608345	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77462657	CTTTCACTGTGGAGG[C/T]CTTTGCTCTGTTCTC	78514
rs229619189	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77268773	AAAAAAGAAAAAAAG[-/A]AAAAAAAAGAGCTAC	78514
rs229620245	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77284403	CCAGCGAGGGGGAAA[-/C]AAAAAACGCAAAGGA	78514
rs229621070	snp	C/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77365316	TTCATTGTCAAAGTG[C/G/T]TATATTAGCTTCGTA	78514
rs229623446	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77359574	TGTACTCAAGAGAAA[C/T]CCTGACTCCAAAACA	78514
rs229625857	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77253171	CATGACTTCATTACT[C/T]ACTTTCTGAGTAGCC	78514
rs229628689	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77434418	CACACATCTATGTGC[C/T]CCTCCAACATACATA	78514
rs229638960	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77281143	TGAACAGTCACCAAG[A/G]CAACAGGAACACCCA	78514
rs229650105	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77315546	TCCCTGAGGCTCAAG[C/T]TTTCCTTCTGTACCC	78514
rs229660613	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77405900	AATTCATATGTGTAT[A/T]TAAAATGCTGGGTCC	78514
rs229664235	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77418528	TAGCCTTGAACTCCT[G/T]ATCCTCCTGCCTCCA	78514
rs229665804	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77472120	TTGCTAAAGATGATT[A/T]TATATATACATATAT	78514
rs229668083	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77461611	TACACACCAAACCAC[G/T]GTCCCCTGCCTGACA	78514
rs229668496	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77505590	GGTCTACATGGAGTT[G/T]CGGGGGCCAGCGGTG	78514
rs229693993	snp	A/C			intron-variant, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77517330	ACCTGACTCCGGAGC[A/C]GAGCCTCCATTCGCT	78514
rs229697536	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77275304	ACATGCAGGTATGCC[G/T]ACATGTACACTTGTG	78514
rs229713205	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77436429	AATGCCATTCTACCA[A/C]AGCATCAGCTCTCAG	78514
rs229713473	in-del	-/GCCT			intron-variant	Arhgap10	GRCm38.p3	8:77506361	CACATGCTCACTGAC[-/GCCT]GCCTGTACAGGCTTC	78514
rs229724049	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77504978	CACAGCTCTGCTCTC[C/T]GGTGACAAGGAATTC	78514
rs229727085	in-del	-/AAAC			intron-variant	Arhgap10	Mm_Celera	8:77329930	TAAAAAAAAAAAAAA[-/AAAC]CATGTTTGTGAGCTG	78514
rs229727846	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77306729	ATACAGACCCTAAGA[A/G]AACACAAATGCCAAC	78514
rs229731986	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77324134	TGGAGAAGCTGCCCA[C/T]CTTTGGCCACAGGAA	78514
rs229753396	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77337792	AGCGCTTTCTCAGCC[A/C]GCAGAGAACCCACCC	78514
rs229753626	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77458759	CATTCTAGGGGAACT[C/T]CAACAGGAATTCAGG	78514
rs229755680	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77388133	AGGTGCCTCCAGCCC[A/T]GTGTCATAACCTTTA	78514
rs229770013	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77318496	CTAACAGCCTGCCTT[C/T]CCAATTCTTTCCACC	78514
rs229770375	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77324656	TACTGATTCTGATAC[C/T]AGAATGTTAGACAAT	78514
rs229771780	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77362589	GACATTGGTTGGCTT[G/T]AAAAAGAAATTAAGC	78514
rs229783975	snp	C/T			downstream-variant-500B	Arhgap10	Mm_Celera	8:77250313	CCATGACTGTCAAAC[C/T]GTGAAGCATCACTGC	78514
rs229793042	snp	A/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77501718	TGCTTCCCTCCCTCC[A/G/T]CCTTTCCTTTTCTTC	78514
rs229798428	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77284621	GGGAGGTTCTGAGAA[C/T]GTTAGGAGAGAGAGC	78514
rs229802960	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77427964	CAATAAAGAATGGAG[C/T]CTGCCCTTCCCTACA	78514
rs229806508	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77474905	CAGAGGCTGGAGATA[-/C]CCCCCAACAAAAGCA	78514
rs229811524	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77414133	TGAGAGAAGCGAGGA[A/G]GAGTAAGGTCCCACG	78514
rs229813728	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77384827	AAGAAACAAAGAAAA[C/T]ACTCTCAGCAGATTA	78514
rs229821048	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77453125	TAAATAAATTCTTCT[C/T]GTTAATTGAAAAGCA	78514
rs229830569	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77348336	TGATAGAGAAATAAA[C/T]CAATTGGGAAACGAC	78514
rs229831563	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77332134	CCACAGAGGTTCCTG[A/C]TGTAGCCGTTAGCGG	78514
rs229852795	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77413363	GCAGAAGCAGGAATG[C/T]GTGCACGCTGTGCCT	78514
rs229855067	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77500330	AAAGTCAGGCCGACC[C/G]CACTACCCAACAGAG	78514
rs229856689	in-del	-/ACTTAAGGGAGAGACTG			intron-variant	Arhgap10	Mm_Celera	8:77334317	AGAGAAAGGGAAGCT[-/ACTTAAGGGAGAGACTG]CCAGTACAGGAGAAG	78514
rs229856836	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77381799	AGCTTAACCCCAGCC[C/T]GAAAAGATCACTTTT	78514
rs229859403	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77496746	ACACTAGGTTCATAA[G/T]GGGACTAAATGTTTG	78514
rs229886635	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77486179	ATGGCCTTTCAGTCA[A/G]TCTGTCTGTCCATCC	78514
rs229889670	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77335248	CAATCTGACAGATGA[-/T]CTATGTGTAATGAAA	78514
rs229890541	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77419248	CAGCCCACACAATTG[A/G]TGAGCCTCCCATTCA	78514
rs229894644	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77280528	ACAACCATCATGTAC[A/G]TCAATAGTCAGGCTT	78514
rs229914559	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77283860	AGCCAAGGTGTAGCA[C/T]AGGCTGTAGCAAGTG	78514
rs229939709	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77267387	CCATAAGAGAATCAT[C/T]TTAGGGTTACAGCTT	78514
rs229944886	snp	C/T			intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77502058	GGCAGTGGGGTCAAC[C/T]GACTCTGGACTGAAG	78514
rs229964790	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77341565	CAGCCACGCCTCCTG[G/T]CCAGTGCTCTGTACT	78514
rs229968622	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77456481	AGGCCTGAAGGCCAC[C/T]ATCAGAGACAGCGCT	78514
rs229972204	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77261593	TAGGTACTTAATAAC[C/T]GTTTCACTAAAAATA	78514
rs229992599	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77324748	TAACTTAAACTGAAG[-/A]AAAAAAAATTCTAAG	78514
rs229995583	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77410629	TGAGCTCACAGGGAA[C/T]GACTTTATGAAACCT	78514
rs230023131	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77452374	TGTAGCCCTGGCTGT[A/C]CTGGAACTCACTCTG	78514
rs230024135	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77323108	TGACACTTAACTCAT[G/T]AGCGAGAAAATGTGG	78514
rs230024559	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77257760	CATTTGCAAAGGGAG[A/G]GGAGGGAGTTTCCCA	78514
rs230025784	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77363561	GAGTTACAAGTGTAC[C/G]AGTGTAACTTCTATG	78514
rs230028894	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77460913	ATAACACAGGATTCA[A/C]AGAGAAGACACTGGG	78514
rs230033905	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77453851	CACCCTGGGTAAGTA[A/T]GCCTATGCATCCTTT	78514
rs230053107	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77262617	GGAGCAGAAGCTAAG[A/C]GCTCATGATCTGCAA	78514
rs230061157	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77497169	TTGCTGGAGTGTATG[C/T]ATGAGCACCCTGTGT	78514
rs230061954	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77319551	AAGCATTCACCGCCT[A/G]TGACAACTTTACAAT	78514
rs230068002	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77414456	CCATGGCTCCTGAGG[A/G]CAGAAGAAAGCAAAA	78514
rs230079158	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77398026	AAAGAGCAATACAAC[A/T]CTTCCCACTGCTGTT	78514
rs230085364	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77317125	TTTTTCTCGGAACCG[A/G]AAGCATCCTAGAAAT	78514
rs230110000	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77251757	GGTAGTAGCCACACA[-/C]CTGGGGATGGGGGAT	78514
rs230123438	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77417928	GAAAATGAGGGCAAA[A/G]GAACAACTTCCAAAT	78514
rs230124127	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77264415	TCCTGCAGCTTTTCC[C/T]ATGGAGGAAGAGAGA	78514
rs230130069	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77479771	AGTAAGATGTGAATT[A/G]TGTCTGCTGGTCTGA	78514
rs230137392	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77317503	TCTTCCAAGTACACA[C/T]GCAAGGTCTCTTCCA	78514
rs230145610	in-del	-/TC			intron-variant, downstream-variant-500B	Arhgap10	GRCm38.p3	8:77358094	CCATCTCAGACCCTT[-/TC]TCTCTCTCTCTCTCT	78514
rs230151224	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77313314	GGATCTGCTTAAGCA[C/G]TCTCTTCACAAGGCA	78514
rs230154408	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77321707	TTTTAATGACGGCTG[-/T]TGAGGCTGCCTATGG	78514
rs230154785	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77347443	GGTTTCTCTTTGTAG[C/T]CCTGGCTGTCCTGGA	78514
rs230161351	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77504428	ACATTACTTTTGAAA[C/T]CTTATTCTGTTAAAG	78514
rs230172694	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77257027	GGATGATGGAAGTCA[A/G]GGAGAACCAAGGACA	78514
rs230180449	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77417645	GCCCTTATTTAAAAA[A/T]AATTAAAAACCACAA	78514
rs230184074	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77373192	CCTTTGTTTTTGTCC[C/T]TGCTATTGTCCCCGC	78514
rs230184179	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77367150	TCTCCAGGATCCCCG[G/T]GTTTAGACAGAAGTT	78514
rs230188693	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485568	CTTTCCAGACCCCTC[C/T]GAATGTCCTCACCAT	78514
rs230190922	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77479110	TTCCCCAAGCTCTGG[C/G]TCCTCCCTCCCTCCC	78514
rs230211190	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77382179	AAAAAGAGAGAGAAA[A/T]TCTAAATGCACAAAA	78514
rs230213472	in-del	-/TAC			intron-variant	Arhgap10	Mm_Celera	8:77407212	ACTCATTGTTGAAAG[-/TAC]TTGCTACTGTTTGAG	78514
rs230217937	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77266694	TACAGTTGCATACTA[A/C]AATATCCAAAACCCA	78514
rs230232130	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77438585	CCATTGAGAAATCAT[G/T]CCATCTTCACCTCAG	78514
rs230241887	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77506397	CAGTGGTGCCACCTC[C/G]ATATCCATTCTCTGC	78514
rs230252483	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77263711	TCTGGAGCAAAGAGC[C/T]GGTTTCATCCATCAA	78514
rs230261447	in-del	-/GGAA			intron-variant	Arhgap10	Mm_Celera	8:77452207	AACACCTCATGACTG[-/GGAA]AGAAAGAAGAAGGCT	78514
rs230274178	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77336117	GGTAAAGCCTATGAA[A/C]GTATTTCAATATTCA	78514
rs230278056	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77411802	ATAACCCCAATAAAT[G/T]ACATACTCTGTATGT	78514
rs230280499	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77475857	ACAATAAGCTCATAC[A/G]TAACAATTGGTGAAA	78514
rs230287995	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77436234	CTTCTCATTAGATGC[A/G]AGGCTATAAGAAGCT	78514
rs230289357	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77443428	ACAGTGCTGCCCACA[C/T]GGGGTGGACACTGCC	78514
rs230294102	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77437805	ATTTCTATTAAAGAA[A/C]TGTGTGAAATATTTC	78514
rs230294147	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77445127	ACAGATAGGGAGTTG[A/G]TAGCCAACTTCCAGA	78514
rs230306917	in-del	-/TACCC			intron-variant	Arhgap10	Mm_Celera	8:77333425	CCAGCATTTCTTCAT[-/TACCC]TACCCATTCATTTGA	78514
rs230308691	in-del	-/TTG			intron-variant	Arhgap10	Mm_Celera	8:77357456	AAAATCACTCTACAA[-/TTG]TTGTGTGGCCTACAT	78514
rs230316023	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77379798	TGCAAGCGTGCTACA[-/T]TTTTTTATTTTAGCT	78514
rs230328767	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77346447	CAGACTGCCCTTAAA[G/T]ACGATTGATAACAGT	78514
rs230329274	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77281546	GACCACAAATATCTC[C/T]AATTTCCTGCCCTTC	78514
rs230336064	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77322336	CCAGGAAGGAGCTTG[A/G]TCATGTCACACCTCG	78514
rs230346387	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77444273	CTCATAAATGCTGCC[A/G]CACTATTTTTAAAGT	78514
rs230346613	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77443025	CAGGTTTTCGGAGAC[C/G]GGGTTAATTTGTCTA	78514
rs230354168	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77451546	ATGTATGGGAAATGA[A/G]CCATGCGGCTTGGTG	78514
rs230372471	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77481881	GTCATAACTAGTTCT[A/G]TATTGGGCATCTCTG	78514
rs230384683	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77339372	ATAGTCCTAATCATC[C/T]AAAATGATTAGGTGG	78514
rs230396946	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77413956	AGGTGTTCGAAACGA[A/T]TGACCTGACCCAAGC	78514
rs230404186	in-del	-/AAGAAG			intron-variant	Arhgap10	Mm_Celera	8:77399387	AGTCCCACCCTCAAT[-/AAGAAG]GCCTTTGTGCCCCTG	78514
rs230416335	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77476154	GGAATACATACATTT[-/A]AAAAATGACACAGAA	78514
rs230418998	in-del	-/CACACACACACACACACACACACACA			intron-variant	Arhgap10	GRCm38.p3	8:77268543	GCGTGAGTTAGACAT[-/CACACACACACACACACACACACACA]CACACACACACACAC	78514
rs230428819	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77457094	GGAATTGGGAGCAAG[A/G]CACCCATGGAAGGAG	78514
rs230430369	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77396539	TGACTATATAGGACA[A/G]TAAAGCAAGTATAAG	78514
rs230436526	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77293153	CATGCTCAGGAAGTT[A/G]GTACCCAGAGCCCAC	78514
rs230440749	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77467298	ACTATATCTATATAA[A/G]TTAATCATTATCCTC	78514
rs230441570	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77460549	CTCAGCCTACAAGCA[C/T]GACACAGACCTTGCA	78514
rs230446622	in-del	-/TTTT			intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77492413	GCACATGATAGGTTG[-/TTTT]TTTTTTTTACCTCTC	78514
rs230447459	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77320938	AGACTGCCAACGTGA[C/G]AAGCTCTACCCAACA	78514
rs230448994	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77327299	TAACTGTTAGTTCTG[C/T]TCTTCCCGAGCTAAG	78514
rs230461504	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77313981	TATGTCTTCATTTCT[C/T]TAACTTAACACTGAA	78514
rs230465595	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77387601	ACTCCAGCTCAGATA[C/T]GACAACCTATAAATC	78514
rs230469778	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77285795	AACGGTGGACACTGG[C/T]TTGTTTTCTTAAAGA	78514
rs230469953	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77293786	AATGCCTAAAAAGTA[A/G]GAGGGCTCATGAGTT	78514
rs230489809	in-del	-/ACTTTGTGAACTAAGCTGGCCTGGA			intron-variant	Arhgap10	Mm_Celera	8:77439048	GCTGGCCTGGAACTC[-/ACTTTGTGAACTAAGCTGGCCTGGA]ACTCACAGAGATCCC	78514
rs230498413	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77466575	CAGGAACAGCGTAAT[A/G]AAATGAAGCAGAGAC	78514
rs230501685	in-del	-/TCTGCCCCTT			intron-variant	Arhgap10	Mm_Celera	8:77438228	CACGTGTAGTCTCTC[-/TCTGCCCCTT]TCTGCCCTCCTCTGT	78514
rs230504776	in-del	-/CAGTTTC			intron-variant	Arhgap10	Mm_Celera	8:77321247	GCCAAGTGATCAATG[-/CAGTTTC]CCTGGTTACTACTAC	78514
rs230532285	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77433912	GAAGAATACAAAACA[C/T]ACAACTGTCCCCTCA	78514
rs230534747	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77490777	AAAATTCAACCTTGT[A/C]ATGAACTCGGGGAAA	78514
rs230547030	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77286540	CTGGAGCAGTAGCTG[A/G]AAGCTCGCACATTGA	78514
rs230554233	in-del	-/GAGA			intron-variant	Arhgap10	GRCm38.p3	8:77482509	AAAGAGAGGAGGGTG[-/GAGA]GAGAGAGGGAGGGAA	78514
rs230554993	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77475463	CACTTGCTGTTCTTG[A/C]AGAGGACCCAGTTTC	78514
rs230576880	in-del	-/AC			intron-variant	Arhgap10	Mm_Celera	8:77472163	CATATATATATATAT[-/AC]ACACATATATACATA	78514
rs230580527	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77480559	GGGATTAAAGGCGTG[C/T]GCCACCACACCTGGC	78514
rs230584892	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77366263	ATGAGCACATCAGGA[C/T]ACTTCCAGTTTCTGG	78514
rs230588778	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77436651	GCCGGGCTGAATATA[A/G]AAGAAACAGAAGGAA	78514
rs230599104	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77255416	GAGGAGCATGTCTCT[C/T]AAGTGGCAACAGTAA	78514
rs230599597	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77510614	CTATCCAAGACCACA[G/T]CTGCTCAGCCTCACT	78514
rs230622527	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77265976	GGGTGAGACAGAGGA[C/G]AGCATGTTCTGAGAG	78514
rs230642356	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77481199	GACTGTCTACACATG[A/T]AATGACGGCTCACTG	78514
rs230642446	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77467496	TCTTCAAAAACCATT[-/A]AAAAAAATATTAAGA	78514
rs230649220	in-del	-/AA			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77515060	ATTTATGGAAGAATT[-/AA]AAAAAAAAAAAAGCT	78514
rs230649518	in-del	-/TA			intron-variant	Arhgap10	Mm_Celera	8:77275156	AAAGAAGCATTTATC[-/TA]TGTAGCAAAGATAAT	78514
rs230655975	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77409041	GACACAGACATTACT[A/G]CCAGGCACTGTCTCT	78514
rs230656958	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77509856	AGCTGAGGTGGGGAA[A/T]CAGACAAACCCAGAG	78514
rs230659536	in-del	-/TC			intron-variant	Arhgap10	Mm_Celera	8:77456702	ATAGGGGAATACATG[-/TC]CCAAAACAAATACAT	78514
rs230668708	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77438572	AAAAAAAATTCTGCC[A/G]TTGAGAAATCATTCC	78514
rs230673481	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77386014	CTCACAGTCCCTATG[C/T]AAATGTATCGCTGAT	78514
rs230681460	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77401381	CATTGCTCCGACCCA[C/T]GGAGCACTGTCTTTC	78514
rs230684829	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77479591	GCATCAGAGCAGAAG[A/G]CAGATGACAGAGGTC	78514
rs230691808	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77342057	CCCACCTCCTCTCTC[C/T]ACCTTTCTGGATAAG	78514
rs230697187	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77274506	GCAGCCCAGCTAGAA[C/G]AGCATATTCTACATA	78514
rs230704829	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77421476	TACACAGCCAGGTAA[A/G]GCAGTTAGCCAATGC	78514
rs230709582	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77338522	TGACTCCTAGCATCC[-/T]CCCCATTGGCTGACT	78514
rs230716133	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77380675	GATCCACAGAGCACA[A/C]AAAAACAAAAAAACA	78514
rs230723583	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77319170	GGTGGGTAGGGGAGT[A/G]GCGGGGAGGGTATGG	78514
rs230724751	in-del	-/GCAGGGAAGAAT			intron-variant	Arhgap10	Mm_Celera	8:77260777	AGGGCAGGAACTCAA[-/GCAGGGAAGAAT]GCTGCTCACGACTTG	78514
rs230736067	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77413062	TGAGTGAAGATGCTC[A/T]CGGAGCCAGAGGCAT	78514
rs230736754	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77474095	CCCAGCCAGTGACTC[C/G]AACTGGCTCAGGTAA	78514
rs230740420	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77396208	CATTTCAAGTATATG[A/G]CAAGTCTGAAAAAGC	78514
rs230747724	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77464769	ACCTAGGGCTGGAGA[A/G]CTGGCTCAGCGGTTA	78514
rs230755618	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77345495	ATCACACGCACATAG[-/A]AAAAAAGCAGCCAAG	78514
rs230759071	in-del	-/A			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77515061	ATTTATGGAAGAATT[-/A]AAAAAAAAAAAGCTT	78514
rs230762698	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77369057	TCAGTGTTCCCACCT[G/T]GCCAATCCAAAGAAG	78514
rs230768853	snp	A/C			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77515585	ACCCTTTTATTCTTG[A/C]GGGGAAGAGTGTAAA	78514
rs230772432	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77439147	CTGGCCAGAGGGTTG[C/T]AATGAGCTCATAGCA	78514
rs230781469	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77385424	ATCTCAAATTCACAT[C/T]ATACTGTGCTACCAA	78514
rs230795493	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77408569	ACAAGGACAGAGAGA[A/G]AGAGAGCTGGGTCCG	78514
rs230806936	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77480059	AGTATCCTGGTTCAG[C/T]GAAGAAGAAGGAACC	78514
rs230818985	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77341502	TGCACTCACATTCCC[C/T]TGGGGAAGGAAAATA	78514
rs230826111	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77362272	ATGCAAGATATGAAA[C/T]GGAATTCAAGCCTTG	78514
rs230841429	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77432443	TGTCACAGTTCCCTA[A/T]AATACAGAGAATTAT	78514
rs230852286	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77326541	TGGTGTAGGCTCACA[C/T]TCATATGACTCGTCT	78514
rs230858919	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77263023	ACTCCACAAGTTCAC[A/T]AACAGGACTCCAGGC	78514
rs230864911	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77336021	acacacacacacacC[C/T]ACCTACATGACACTC	78514
rs230869600	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77288703	AGAGAAAATCTAGTG[C/T]TCCTCTTACAGCCGC	78514
rs230870300	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77370807	AGGACCAGTCGACTT[C/T]GTGCGGACCGACAGG	78514
rs230872933	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77474648	ATCCAAGACAGTACA[C/G]ATGGACATGGAGACT	78514
rs230877552	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77271526	ATGGGAGGTTTGTAG[A/G]GTATGCAGGAACAGA	78514
rs230877588	in-del	-/GG			intron-variant	Arhgap10	Mm_Celera	8:77287928	AAAAAAAAGGGAAAG[-/GG]AGAAAGAGAAAGAAA	78514
rs230893702	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77372254	AGAAGTCTAAGCCCT[A/G]CCTGTCCCTGGATCT	78514
rs230896681	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77335661	TACAGTGATGGCGAA[A/G]CTCGTGTCCATTGTG	78514
rs230897517	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77514590	TGGAGTTACAAAGGA[C/T]TGTGAACCACCTAAT	78514
rs230899696	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77318751	TGCTTCAAGAGCAAA[-/G]GGGAAGCTTTTGCTC	78514
rs230902120	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77439676	ACTTGCATGCACACA[C/T]CCCATACATGCACAC	78514
rs230914426	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77281002	TGCGAGCTCTCTACC[A/T]CAGGGTCCCAGCCCC	78514
rs230930720	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77340556	GAGGTTCTGCTGGGT[A/G]AGGCTTTTCACCCTG	78514
rs230939918	in-del	-/TC			intron-variant	Arhgap10	Mm_Celera	8:77327807	GATTCATCCTAGTCT[-/TC]TCTCTAAGTTTCATC	78514
rs230941274	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77460729	AAGCACTCTGCACGT[C/T]CTTTGCAAACCTTAG	78514
rs230960841	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77504314	CCTTCTGTAAGTCTT[C/T]TTTAGGAGAATACTA	78514
rs230963197	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77287797	AGAAACCCTGTCTCG[A/G]AAAAAACAAAACAAA	78514
rs230969569	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77447006	AGCTACCCCTCTTCT[-/C]AAATATCACTTTTGA	78514
rs230970354	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77430489	AACTCCCACCAGCAC[C/T]ATTACAAGCCCAGAG	78514
rs230972199	in-del	-/GCCAGACA			intron-variant	Arhgap10	Mm_Celera	8:77380479	AAACCCAGAATACCT[-/GCCAGACA]GCCCCACCCAGTCGG	78514
rs230973893	in-del	-/CCACAG			intron-variant	Arhgap10	Mm_Celera	8:77486134	TGCAAACTGGATAGA[-/CCACAG]CCTGAATAATGGCTG	78514
rs230990093	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77412136	GACAAAGCAACGGTA[C/T]AATGATTATTCTACA	78514
rs230994513	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77460161	TAGAAAAATCCCAAA[A/G]GAGTCGGGGGTTGGG	78514
rs230998176	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77416759	GGGCTGGCAGATCCA[G/T]GAGAATCACTGATCA	78514
rs231000520	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77344378	GAATGAAAGTGCTCA[A/G]TTAGCTATTAAGTTA	78514
rs231005584	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77361902	GAGAAAGAAAGAACA[C/T]CTTCTCCCTGACTAC	78514
rs231010910	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77279721	CAATGAATCTAAGGC[A/G]GGCTCCCCCCACCTG	78514
rs231015366	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77298458	ACCAAAGTTATAAAG[A/T]AGAAAAGAGTAAAAT	78514
rs231019941	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77505846	TATCTCCGAGCAGTC[A/G]TAATCTACTCATTAT	78514
rs231037141	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77317474	AAGAAACCTTACCAC[A/G]ATCATCTGAAACCTC	78514
rs231045177	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77459505	TTCGCCATTTACAGA[G/T]TTACCTTTTGTGGGA	78514
rs231051008	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77345047	CTGTAACCAGTCTCC[C/T]CAGGTACAGGCTCCT	78514
rs231056437	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77449055	CCTGTGCACACTGCC[A/G]CATCCCTGGCCCTGT	78514
rs231067269	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77291444	AAGCTAAGACTTCTA[C/T]ACACACACACATCTA	78514
rs231073355	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77375929	GTCACAAACGGATCC[A/G]ATTTTGGTGTCAACA	78514
rs231076190	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77262331	TCAATATCACTGAGC[A/G]ATGCTATCGCACACT	78514
rs231078171	in-del	-/GCAATACCAG			intron-variant	Arhgap10	Mm_Celera	8:77463739	TTAGAATGCCAACAA[-/GCAATACCAG]GTGAATAGTGTCTTT	78514
rs231084078	snp	G/T			utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250518	GCCCGGGGAGGGGGT[G/T]GGGAGGGGGAGGAGA	78514
rs231085203	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77415915	ACAGGCAGTAAAACA[C/T]CTCAAAAAAAAAAAA	78514
rs231097603	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77325435	CCTCTGCCATCTTCA[C/T]TGGCAATTCACACAT	78514
rs231120900	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77255005	TTCACAAGATGGGAG[A/G]TAAACTCTGCACTGA	78514
rs231133405	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77414698	CCAGCCTGGTCTACA[A/G]AGAAAGTTCCAGGAC	78514
rs231142834	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77346264	GCTGATGGGGAAGGA[A/T]CACTCACTTGGTTAG	78514
rs231172834	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77383600	AAGCTTTCAAGAACC[C/G]ACTATGGCTAACATT	78514
rs231174657	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77431422	CAACAGACAGGACAG[A/C]AACTCCCCATACGGT	78514
rs231175541	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77499701	AGGGTCCCCTAAGGC[C/T]ATCAGAAAACTCGTA	78514
rs231190397	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77292137	CATTCATAGATCCAA[A/G]ATGCAACAACAGTCA	78514
rs231206459	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77412408	TTTTGGAGATGGGGG[-/A]AGGAGGGTGTTTTTC	78514
rs231218433	in-del	-/CC			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485070	CAATTACAGTCACAG[-/CC]CTCTTCCCCTCAGCT	78514
rs231223617	in-del	-/AGAG			intron-variant	Arhgap10	Mm_Celera	8:77408562	AACGCTCACAAGGAC[-/AGAG]AGAGAGAGAGCTGGG	78514
rs231226883	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77315092	TTCACCGTGCGCTAG[-/T]TAAGTCCCATCCATC	78514
rs231236398	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77351238	AAACCATCTCCAGAC[C/T]ACAACATCTCCAAGC	78514
rs231245289	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77275273	AGAGAGAGAGAGAGA[A/G]AGAGAGAGAGAGAAT	78514
rs231246222	in-del	-/ATCAAGCACTACCGGA			intron-variant	Arhgap10	GRCm38.p3	8:77251495	GGCCTGCTTCAACCC[-/ATCAAGCACTACCGGA]ATCAGGCACACTGAT	78514
rs231255961	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77270385	AGCCGGTGGAAGGCT[C/T]AGCCCTAATAAAACC	78514
rs231264615	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77455352	ATGAGCCGGAGACAC[A/G]GCCACAGGCCAATAC	78514
rs231283649	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77421768	AGTTGAAAGCAGTGG[-/T]TGGCTCACGTGACGC	78514
rs231290065	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77441349	AGGGACAGGACTAGT[A/G]AGTGACAGGCAAAAC	78514
rs231292304	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77384414	GGCATGCGTAGGACC[A/G]TGAGCAAGAGCAACC	78514
rs231297588	snp	A/G/T			intron-variant	Arhgap10	Mm_Celera	8:77417875	CACATGCAAGCGTGC[A/G/T]CACGTGAGGGCACAC	78514
rs231298462	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77404969	TCTGTAAGCAGAGAG[C/T]GAGCCTGGACTCACA	78514
rs231305079	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77264676	ACACACAGACACACA[C/G]AGAGAGAGAGAGAGT	78514
rs231316621	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77265914	TCATGACACATGCTG[C/G]AAGACAAGCCCAGAG	78514
rs231327388	in-del	-/TCTCTC			intron-variant	Arhgap10	Mm_Celera	8:77255568	AAACCTGTGCACGAG[-/TCTCTC]TCTCTGTGTGTGTGT	78514
rs231335387	in-del	-/A			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77502370	GAAGATCCAGAAGCC[-/A]GCACGATTTGTTTTA	78514
rs231342967	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77330779	AGTAATATAGTGGAG[A/G]TTGTGGCCCAGATTC	78514
rs231347052	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77447444	TCTTCCTCTCATCAG[C/T]TCACTCCAAGGAATT	78514
rs231352588	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77440827	TTACTATTAAAAAAG[C/T]CTTGCCAGTGACTGA	78514
rs231370015	in-del	-/AAAAA			intron-variant	Arhgap10	Mm_Celera	8:77381964	TCAGAATGTAACATT[-/AAAAA]AAAAAAAAAGGGGGG	78514
rs231391128	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77399837	TTCAAGGAATGTCAT[A/G]GGAGAGGCTCTGCTG	78514
rs231392620	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77463701	GATTAGCATTCTGCA[A/T]CAGCATAGACTCCTT	78514
rs231397163	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77324836	AGATCATAATACACA[A/G]GTTGGTCCAAAGCTA	78514
rs231397223	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77331345	GATGCGGTACGACCG[C/T]GGCTAAGTCATGTCC	78514
rs231398136	in-del	-/TATA			intron-variant	Arhgap10	Mm_Celera	8:77356069	GAAGAACGCCTATAT[-/TATA]TATAGGATCAAATAA	78514
rs231399786	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77368476	CTTTTCACTGGTGCA[A/G]AAACGTCTGTGTAAG	78514
rs231403858	in-del	-/CTCCCACCCTCA			intron-variant	Arhgap10	Mm_Celera	8:77326647	CATGACCATTGCTTT[-/CTCCCACCCTCA]CTAATCTGATAACTG	78514
rs231406843	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77447134	TTTCACCCAAGATAG[A/G]GTTTCTCCGTGTAGC	78514
rs231417384	in-del	-/GTGTGTGTGTGC			intron-variant	Arhgap10	GRCm38.p3	8:77489278	TGTGTGTGTGTGTGT[-/GTGTGTGTGTGC]GCGCGTGCACATGAG	78514
rs231420288	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77437266	CCCAAACAGTGCCTA[G/T]CGAGTCTCAAATCTA	78514
rs231422859	in-del	-/C			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519191	AGGGGGAGGGAAAAA[-/C]TGGAGACTGAATTAG	78514
rs231425344	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77416664	GGACGGACAGACAGA[C/T]AGGCAGGCGGACCTC	78514
rs231448345	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77265096	CAAAAACAACTTAAA[A/G]CTCACAGCAGAGAAA	78514
rs231448346	in-del	-/CT			intron-variant	Arhgap10	Mm_Celera	8:77273266	GGGTGCATGGTGAGA[-/CT]CTGCATCCTGGAGGT	78514
rs231453297	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77460102	GCAGCCTGCTCTACA[A/G]AATGAGTTCCAGGAC	78514
rs231458641	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77297716	CAAAGCACAGACAAC[A/G]GTGGTTTGGAAGGGT	78514
rs231473202	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77295849	TGTGCCCACAGGGTA[-/G]GTCTCTATAAAAACA	78514
rs231474476	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77316855	GAGAAGCCCAGCACT[A/G]CATTTGAAAGTGCTT	78514
rs231477896	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77502824	CGGCCCAGCAGCCAG[C/T]GGTACCAAGCTCTGG	78514
rs231482557	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77396443	GCAAACGGCAATTCT[C/T]TACCTGCTGAAGCAA	78514
rs231485396	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77400308	GGAGACACCGTCTAG[C/T]TTCACTTATTGGGGG	78514
rs231492663	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77398951	CTGTAATAGCCCAAC[G/T]GGGAAGCTAAGCTAC	78514
rs231497568	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77396984	ACATGTGAAAGGATG[C/T]GTGGTGTTTAGAAGG	78514
rs231514069	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77412625	TTCCCCACATCAGCA[C/T]AGCACGAGCATGGGA	78514
rs231528674	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77436559	TAACTACTGTTTAAC[A/G]GATCAGCCCAGGTTA	78514
rs231532641	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77297018	ACGATTCAGTGATTT[C/T]TGAATTTTTGGCATG	78514
rs231532662	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77288985	GCAGTCAGATCTCTG[C/T]GAGTTCAAGGCCAGC	78514
rs231540987	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77346879	GAAGAAAAAGTGTGC[A/G]TTTTACAATACCTAA	78514
rs231558329	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77374958	ACCTGTCTTCAAGAA[A/G]CTGCATGGGATCACT	78514
rs231559516	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77478146	CCAGACTACTGGTAA[C/T]TACAACGCACAATAA	78514
rs231562474	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77482029	AGATTCCGCAGCCTC[A/G]GGGCTTGGTGAAGTA	78514
rs231579672	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77384048	TGCTTCCCAAGTGCA[C/T]GCGTCCTGAAGAGCG	78514
rs231581208	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77499212	AATCACAGCATGAAG[A/G]GAAGGGAGGGCATGT	78514
rs231583862	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77372160	CTATTTCATGAACAA[C/T]CATCCAGGGGAAATG	78514
rs231585776	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77443365	CCACAGTTAAAGAGT[A/G]TATGATCAGTCATGG	78514
rs231600224	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485682	GCACCCTCGGGGCAG[A/G]GATTTCAAGAGACTG	78514
rs231609169	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77289831	CTCTAGGAAAGGGGA[C/T]GCCCACGCTCTAATC	78514
rs231618551	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77423926	TGAGCAGGTGTGCAA[-/G]TGCATGACACATGAG	78514
rs231619479	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77410843	TTTAAGACTCCTCTT[C/T]GTTAAAGAATCTAAC	78514
rs231622040	in-del	-/GA			intron-variant	Arhgap10	Mm_Celera	8:77404077	AATTGAAGGAGGGGG[-/GA]AAAAAAAAGACAGCA	78514
rs231623515	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77287254	AGACATGCAGACATG[A/G]ATTCTAACATCAACA	78514
rs231628082	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77461196	CAGCAGAGAAAGCCA[A/G]GGAAAAGAAAATAGA	78514
rs231640606	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77366092	ACATACTGGCTGCCA[A/G]CGAAGTGTCTCTAAT	78514
rs231641818	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77506093	CCCCACCCCCCCCCC[A/C]GCCTCTAGAACGCTG	78514
rs231643241	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77370104	ATTCACAATCCTGAG[A/G]GGGGGGGGGGCGGGG	78514
rs231645187	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77375305	TTTTCAAGGCAGCCA[C/T]GACACCAGGTAATGA	78514
rs231656936	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77426503	AGTTAACTTACCAGA[A/G]GATAAAAATATGAAA	78514
rs231659228	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77488832	TAAGTAAGATGGGTA[A/G]CAGAGCAGTGGTATG	78514
rs231661332	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77268326	AGTAACAATAAATCA[C/G]AACAATGGCATCAAA	78514
rs231667831	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77321375	GACACGTCTTATGAA[A/C]GACCCGGTCATGGAC	78514
rs231671858	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77497107	GCCACAGAAGGACTA[-/T]TTTTTCATGAGTGTG	78514
rs231677943	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77411489	ACGTGCACACACATG[C/G]ACGCACACACGTACA	78514
rs231691109	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77416118	TGTCTGGATAAGGCT[-/AA]GGGGGGGGGGGGGGG	78514
rs231692637	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77268930	CTGTCGCCCCACAGG[C/T]AGTCATACTCCACAG	78514
rs231692884	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77513250	CTGGGTCTTCCCAGC[A/G]CAGTTGGAACTGAGT	78514
rs231706601	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77510247	CTCTTAAAACACTGA[-/T]TGATCCTCCTCAGGC	78514
rs231708513	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77281792	CAACAGAATAAGGAG[-/A]AAATTACTGCCAGAC	78514
rs231712156	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77425873	AAACAGGCCTAGCTG[A/T]GTCTACTGTGTGGGC	78514
rs231712958	in-del	-/TG			intron-variant	Arhgap10	Mm_Celera	8:77505613	CAGCGGTGTCTACAC[-/TG]TGAGACCCTTTCTCA	78514
rs231713840	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77366779	AGCATGCTAGGCAAG[C/T]GCTGTACCACTGAAC	78514
rs231726020	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77488188	TAAAGGATGTACCCC[A/G]CCTCTACTCTAGTAT	78514
rs231727384	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77388950	AATATTGCGGGAGGG[C/G]TGTCTTACCATGTAG	78514
rs231739603	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77404161	CCCCCTGCTGCTCAC[A/G]GTCCCCTTGGTTCTC	78514
rs231745701	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77482626	AAGTGGGAAAACCAC[C/G]CAGTGACTTTTCAAA	78514
rs231747863	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77344910	AAAAAACAGAAGAAA[C/T]GAACAGTCTTCAGTG	78514
rs231766351	in-del	-/AAG			intron-variant	Arhgap10	Mm_Celera	8:77285757	ACCTGCATTAGAAAC[-/AAG]AAGACAGAAGACTAC	78514
rs231775230	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77512715	GTGGCCTCCGGCCTA[A/C]AACAATGCATGGCTC	78514
rs231788787	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77292032	AATAGAATTAAATAA[C/T]TATGGTTCCTATTAT	78514
rs231791438	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77460309	ACACTCAGCCTCCAG[A/G]CCCATTTATTACAAT	78514
rs231796387	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77398521	GAATAAACTGGTATA[G/T]TAGTCGGTGTGCACA	78514
rs231796430	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77404614	CCCGGGCTCACGAAG[C/T]CTCTCCTGCAATGCC	78514
rs231796691	snp	A/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77489298	TGTGTGCGCGCGTGC[A/G/T]CATGAGCGTGCATGT	78514
rs231800267	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77266315	CTGTGCCTGAGTCAG[A/G]CTTTCTCAGAAAAAG	78514
rs231801245	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77446741	AGGCATGCCGTGGGT[A/T]TTGTTAAAGTGGCAA	78514
rs231803413	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77338166	CCACAGTTTAACATT[C/G]CACTGATGGCTGCTG	78514
rs231806655	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77467786	AGCAGACTGACCCTT[C/T]GGACAAAGGAATGCG	78514
rs231810413	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77251135	AACACCAAAGCTGCC[A/G]CAAAGGTTCTGTCTA	78514
rs231814449	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77356831	GAAGGAAGTGGCACC[A/G]CTGTGACGGGCTACT	78514
rs231816783	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77349261	ACATGTTCCCATACT[A/T]ACAGCTCAGTTTTTC	78514
rs231818975	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77316184	CAGGAGCAAAGGGCA[C/T]GCTGTGTCTGCGCGT	78514
rs231821864	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77284911	AATGATTTAGAGATG[C/T]ACAATACAGACAACA	78514
rs231835599	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77260339	AAAGAACAAAAGACT[A/G]GAGTCTAAAGGACAT	78514
rs231840124	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77373399	TCATCTCAAACCTCA[A/G]CCTGGGCTAACGCAC	78514
rs231845954	in-del	-/CAA			intron-variant	Arhgap10	Mm_Celera	8:77382039	ACATAAGCTCAAGCG[-/CAA]TGCGCGCGCACGCAC	78514
rs231848214	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77379452	GCCTCTGAAGCGTCT[A/G]CACACACCCCAGCCA	78514
rs231856728	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77467399	GAGGCAGAGGCAGAT[A/G]GATTTTTGTGAGTTT	78514
rs231866069	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77473445	CTAATCAACAGAGTT[C/G]TGCTAACTGGAAAGC	78514
rs231878175	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77364651	TGCCAAGGAACGCTG[C/T]GTTATCAGCACAGAT	78514
rs231885644	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77508731	AAACACTGTCACCCC[A/G]CAGGTTCAGACACCC	78514
rs231890971	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77446209	CAGCCATACTTCAGA[C/T]CTTTGCCTATTCTGA	78514
rs231899826	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77350047	GTGACAGAGTCTATG[A/G]CATCTACTGATAATT	78514
rs231903020	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77374068	CATTTCTTGGCTACT[C/G]TGGCCTGCTGGCTTT	78514
rs231907493	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77452129	AAAAAAAAAAAAAAA[-/C]CAAAAAACAAAAAAA	78514
rs231908838	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77320088	GGTCAGGCAGTTTTA[C/G]GGTAGCAGAAACTAT	78514
rs231909544	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77472938	GAATGCCTACACTCA[C/G]GCGCATGCACATGTG	78514
rs231921447	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77338482	ATCCTTCCCATTGGC[C/T]GACCCCTAGCACTCT	78514
rs231932771	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77478611	TACTTCCTAAACCAC[A/G]GCCCTCAGAGTTCCC	78514
rs231941322	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77273281	CTCTGCATCCTGGAG[A/G]TGAAGATTAAGCTAG	78514
rs231946939	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77265037	AGCAGATGGGTCAGC[C/T]TTGAGCACTGCTGGC	78514
rs231955950	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77374377	GCTAAGATCGGTCCT[A/G]GCCCATTCAGCTGCT	78514
rs231970971	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77422814	ACGCTGCTGCAACAG[C/T]CCTACTCTCCTCGTA	78514
rs231978674	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77285564	TAAAGTCTACTTCTG[C/T]CATTAATAAAGGAAA	78514
rs231982689	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77451157	ATCTTTCCGCACATT[C/G]CTCTCTCCTCAATCA	78514
rs231988304	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77445412	CAAAACTGTTTGGGT[A/G]GGAAGGTCTGCGCTT	78514
rs232001179	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484398	ACTACGCATGACAAA[C/T]GATTACTAACTGGGA	78514
rs232004776	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77346622	TAGCAGCACAGGCAA[C/T]TCCAGTAGCCAGCCC	78514
rs232013766	snp	C/T			intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77492985	AATTGTAATAATAGT[C/T]GAGTAGTGGTGGTAT	78514
rs232014042	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77435413	TTCCGAGATTCTGTA[C/T]GTGCAAAGCTACCTA	78514
rs232030192	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77400775	TTGGGTGTGTTTTCC[C/T]TCTTTGTACACATCT	78514
rs232055594	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77463098	CATGTGAACAAGCTA[C/G]CAAAGTCTACATGAG	78514
rs232055698	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77469845	ATGATTCCACCAGGC[A/G]TATGCTCTTAAGTGC	78514
rs232060921	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77347304	CAACTAAGATGACTG[C/T]ATAATGTTGAAGAAA	78514
rs232062220	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77330020	AAGCCGTTAAGCTTC[A/G]CTGCTGTCCGCTCTC	78514
rs232065299	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77323724	GCCCAGACCCCACAT[C/T]CACGTGGAAAGCACT	78514
rs232065853	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77514119	ACCATCCAATACTCC[A/G]CCTCCACTCTAACCA	78514
rs232073915	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77476287	GTGTGATAAAAGTAT[-/A]TAAAAATGCATAACA	78514
rs232080751	in-del	-/TTCTG			intron-variant	Arhgap10	Mm_Celera	8:77369421	TCATTTAATTGTGTC[-/TTCTG]TTCTATTTTCGTGGT	78514
rs232116626	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77372528	CTCTTGAAATTTAGA[C/T]AGTGGTTAAGGCAGA	78514
rs232121885	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77348077	TTTTTTAGCTTTTCA[A/C]CTTATACTGTTTTGA	78514
rs232137100	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77469560	ACATCATGACGGGAG[A/G]GTATGTACTGGGCTG	78514
rs232141190	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77378926	AGGGAGGGGCTACAG[C/T]GAAGCACAGGGTATG	78514
rs232145625	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77324062	AACGGCCTCCCTTGT[A/G]GCCTAGCAGTCTCCG	78514
rs232162872	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77328201	GGATGTAAAACTGGC[C/T]TTTCCTGACCATCCC	78514
rs232168028	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77458373	TTTAGTCTCCTCTGC[-/AA]AGTCTTCCCTCAGAA	78514
rs232183973	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77371055	AGTAGCTAGCTATAT[A/T]ATTATACATGAAAGA	78514
rs232187695	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77258311	AGCTTGCTTCTTGGT[C/T]ATGATATGTGTGCAG	78514
rs232190718	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77440510	TAAGAGCGCTGACTG[A/C]TCTTCCCTGGCTCAG	78514
rs232209365	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77325784	GTAGACAGAAGAATG[C/T]CCATCACATGCAACC	78514
rs232231735	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77468427	TTGGAGTACACAGGG[C/T]GGTGTGAAATTGTGT	78514
rs232243075	in-del	-/TA			intron-variant	Arhgap10	GRCm38.p3	8:77407892	TTTTGCTATATATAT[-/TA]AAAAAAAGTAGAATA	78514
rs232254675	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77423253	CCAGAAGAGGAGGCC[A/G]TGTGGACAGAGAGCT	78514
rs232263607	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77399417	GGAAACATTAAAATT[C/G]AGGAGTTCCCATCAA	78514
rs232268448	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77415045	ATTATTCATTGCGGT[A/T]AGATTCCTCCCAAAC	78514
rs232276652	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77440070	GGCTATAAAAGCATC[A/C]TTAGACAGAATGTTA	78514
rs232280395	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77350823	AATCTAGCCAGTGGA[A/G]TTGAGTTCTAATTTT	78514
rs232284414	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77356294	ATCCTTTGTAACTCC[A/G]GTTCCAAAGGGAACA	78514
rs232293590	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77441218	GCAAGACCGTCCACC[G/T]GCGTGAGCCTCCTTC	78514
rs232296813	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77458649	ACCGTGATGAGGTTA[C/T]CTGCTTGCCCAATCC	78514
rs232301408	in-del	-/GAACAATGTTGAAGT			intron-variant	Arhgap10	Mm_Celera	8:77419385	AGTCCCCTACCATCG[-/GAACAATGTTGAAGT]GGACTGGAACACATG	78514
rs232302356	in-del	-/AAA			intron-variant	Arhgap10	Mm_Celera	8:77382160	CATGAATCCTTATTT[-/AAA]AAAAAAAAGAGAGAG	78514
rs232304910	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77354170	TCAATGTTTGTATTA[A/G]TAAAAGGATAAAATA	78514
rs232309057	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77288843	GAAACCGTTAGAAGC[A/G]AGACAGAAATTAAAA	78514
rs232309651	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77422638	GTATGTGTTGTAGTA[C/G]AGAGGCTGTCTAGAA	78514
rs232311873	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77395932	ATGTCAGACAGCTCT[C/T]TGGCTTCCTACAGAC	78514
rs232318629	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77387367	GGCAAACATGGGTGC[C/T]AGGATCTGTGCTGTG	78514
rs232323482	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77421259	GGTATGGCACACATG[A/G]ATGGACTCTTAGGCT	78514
rs232335179	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77482020	TCCCAGAGCAGATTC[C/T]GCAGCCTCAGGGCTT	78514
rs232336242	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77342920	GTAAATTTATGTGTG[C/G]CCAAACTGCTCCAAC	78514
rs232354116	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77464280	GGGTTTTGAGAAGCA[C/G]CTGGGGTCTGTGGAG	78514
rs232358474	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77290381	TAGTCCTGTCAAGAG[A/T]AGTCACCAAACCGTC	78514
rs232361312	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77292717	CTCACTTTCACCACA[A/G]TGCAGCTATGTGGTT	78514
rs232396434	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77424227	CAGTAGACCAAAAAG[C/T]CAACAGCTGCCCTTG	78514
rs232402961	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77333302	TCTTAACCACTGGAC[C/T]GTCTGTCTAGCTCTT	78514
rs232412431	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77443707	AAGTTATAGCCGGGC[A/G]TTGGTGGCGCACGCC	78514
rs232412590	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77450191	TCTGAAACCCTTGAC[A/G]CTTCATTGCTGAGTT	78514
rs232418684	in-del	-/GCG			intron-variant	Arhgap10	Mm_Celera	8:77335963	ATTTGAATATAATAA[-/GCG]ATTCTCTCTCTCTCT	78514
rs232447903	snp	A/G			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519838	GTCTGTCTCCAAGCC[A/G]ACCCACATTGTAGAA	78514
rs232451738	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77328777	GTATGATGTCCGTTT[A/T]CTTCTCTACACTAGT	78514
rs232454314	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77324498	TCTCCAGGATTTCTA[G/T]TCCCACCCAGAAGAT	78514
rs232455074	in-del	-/AT			intron-variant	Arhgap10	Mm_Celera	8:77418512	TCTCAAAATCACTAC[-/AT]AGCCTTGAACTCCTG	78514
rs232455882	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77326142	AGGTCCTGAGTTCAA[C/T]TCCCAACAACCACAT	78514
rs232459910	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77419715	TGCCCAAAATGTAGG[A/G]ACGGAGAAATTCCAT	78514
rs232463968	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77333768	ATGTACGCAGGCAAT[G/T]TTCTGAAAATAGAAC	78514
rs232481957	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77269319	GGAGGGTAGCTAAGG[A/G]AGCCTCCACAGCCCT	78514
rs232482224	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77462905	GTAGCCAAGGGTCTA[A/C]AAATCACACTTTGAA	78514
rs232491713	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77464752	GACTTCAAAAATGCC[C/T]TACCTAGGGCTGGAG	78514
rs232496917	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77365254	CTCTGATAACTCGCA[A/G]CAGCAGCATTCCTGC	78514
rs232509253	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77329447	CATGGGAGACTGGGA[A/G]GAGAAGATGAGTCAA	78514
rs232519401	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77400925	GCTAAGGGTGACAGT[A/G]CGGATCTGCATCCTC	78514
rs232522263	in-del	-/ACACACATACACAT			intron-variant	Arhgap10	Mm_Celera	8:77385257	CACACACACACACAC[-/ACACACATACACAT]ACACTCACTTTACAA	78514
rs232528934	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77435884	ACATTTAACTAGGGC[A/T]GGCTTATAGTTTCAG	78514
rs232531191	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77509560	GTGCAGCTAAAGATT[-/A]AAAAAAAGGGGGGGG	78514
rs232536799	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77320572	AAGCTGAGAGGCAGC[A/G]GCAGGACACAATCTG	78514
rs232538123	snp	G/T			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519297	AGGCTGCAGTAATCC[G/T]CGATCCCATAAGCTG	78514
rs232551667	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77400281	GATTTTAATTCCATC[C/T]AAGGAACCCTAGGAG	78514
rs232559552	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77265503	TGCCAGAATCCATGG[C/T]GTAGGTAGGAGTATT	78514
rs232564746	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77263645	TCTGGACTAGGTTTT[G/T]GGGAATATTTGTAGG	78514
rs232578025	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77401323	ACTGAAAGCTTGTCT[C/T]TCTGAAACCCTGGTT	78514
rs232581635	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77305763	GAAGTACTGACACAT[C/T]GGTTTGTAGGAGGGA	78514
rs232593865	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77450539	ACCAAGAACTCATCA[C/T]ATAACCACCATGGAC	78514
rs232597579	snp	A/C/G			intron-variant	Arhgap10	Mm_Celera	8:77481167	TACACATGAAATGAC[A/C/G]GTCTACTATTCACAC	78514
rs232615527	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77307134	TGTCAAAGACAAACA[C/T]GACCTCAGAGTAAAG	78514
rs232620213	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77447033	TTGAGGGGTAGGTTT[G/T]TTGTTTTGGTTTGGT	78514
rs232655376	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77487725	CCTAACAGCCTCACT[A/C]TCTGTCCTGCTAGTG	78514
rs232658487	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77293910	TTTCCTCTTGTTTGA[A/G]AGTTTGGGGACTACT	78514
rs232658597	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77310050	CCATATGTAAAAACA[C/G]TGGCTTGACACCACA	78514
rs232670746	in-del	-/AG			intron-variant	Arhgap10	Mm_Celera	8:77319311	CTCTATCTCAATGTA[-/AG]AGTTCCAGAATCAAC	78514
rs232675522	in-del	-/A			intron-variant	Arhgap10	GRCm38.p3	8:77441743	TCCCCACCCTCCCCC[-/A]CCCACACACACACAC	78514
rs232679869	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77488919	CAATGCCACCAAGGT[A/G]TCCTGCATCTTACAA	78514
rs232683082	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77496874	TGCCTCACAGGTGCT[A/G]GAACTAAAGGCGTGC	78514
rs232695092	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77293034	ACAAATCATTGGTCT[A/G]CGTGGACTGCCACAT	78514
rs232700308	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77460403	CAAAGTAGCAATATT[A/G]GCAAGAAAGAAACAT	78514
rs232708433	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77290999	TTTCTTTGAAAGCAC[A/C]CCAACAGATGTATTG	78514
rs232714859	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77294530	TAGTGTCCATTGCTG[A/G]CATGTGGCACTGAAT	78514
rs232742442	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77283809	GTAAGAGCCAGGGAA[C/T]GTGGCCCAGGAGGGC	78514
rs232744167	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77271119	GGAGAAAGGAGCCTC[A/C]CTTGAGGAAATGCCT	78514
rs232745514	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77374615	CAGCCCACGCTTACC[C/T]TGAGGGGCAGTTATA	78514
rs232764565	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77405414	ATGCACACAGAAATG[C/T]GGTGCCCACAGAGGC	78514
rs232770079	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77413811	AAACAGTCAATCGAG[A/C]GGGTGAGCTGGTGGC	78514
rs232771236	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77271467	TATGGGGGCCTCTGT[A/G]AGGCATGGGAGGGAC	78514
rs232771829	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77516844	AGACTCACTACAGCT[C/T]CGATACACCTCTCTT	78514
rs232776475	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77513529	AAAGAACACCTCTGA[A/G]CCATTACACAGAAAG	78514
rs232788161	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77428185	TCCCCAGAAGCGACT[A/G]TGACAGACCTGGGCT	78514
rs232792291	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77325277	AAAGGCCCTTAGGTC[A/C]TCAGGCTGTGAGTAA	78514
rs232822318	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77406056	TGACAATTTAAAAAG[C/T]TACTCGGCCAGGCGG	78514
rs232836989	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77270276	CAAGTAGTCGCCCCT[C/G]AGGAACCTCAGTCTG	78514
rs232841784	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77418124	ACTCACAATAAAGGA[C/T]GGGTGTTGCTGTCAG	78514
rs232848045	snp	A/C			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77515770	CCCCCCCCCCCCCCC[A/C]CACACACACACACAC	78514
rs232859759	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77295278	GTTACCCTAGTTCTC[A/C]TTCTGAGGACATAAA	78514
rs232861108	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77444093	TTCCATCTCCCCCAC[A/G]CACTGTTCCTGCATC	78514
rs232868875	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77315289	GTTTATCCTTCCTGT[A/G]CACCACAAGTAAAAC	78514
rs232876270	in-del	-/CT			intron-variant	Arhgap10	Mm_Celera	8:77445953	GATAAAATATAAAGG[-/CT]CTGTGTGTGTGTGTG	78514
rs232880714	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77398300	GGACCTTTAGAAGAG[C/T]AGTCAGTGCTCTTAA	78514
rs232883676	in-del	-/TT			intron-variant	Arhgap10	Mm_Celera	8:77470955	CAGCCAGTGCTTTTG[-/TT]TTTTTTTTTTAAGAT	78514
rs232884153	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77264398	TTTGCAGTTGACACA[C/G]TTCCTGCAGCTTTTC	78514
rs232885312	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77470673	ACCCCGAGAATTTAG[A/T]TTCGAATGGTAGTGT	78514
rs232893874	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77349782	CATAAGAAAGGAAAA[C/T]GAGACATCAAACTGC	78514
rs232898649	snp	G/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484821	AAGAAGGGGACAATT[G/T]AAAGGCAGAGAAAAT	78514
rs232901468	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77348837	TACAAGTATTCTCGT[C/T]TGAGTAACTGCTGGG	78514
rs232915489	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77296942	GGATCACTGAAAGCA[C/T]GAGCCCAACATGGCC	78514
rs232915849	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77450084	CAGTGGGGGATAGGC[A/G]TCAATGAAAATAGTA	78514
rs232919292	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77295940	TTCAAGGTGGGGTTC[G/T]GTGTTTGGAGACTGT	78514
rs232925307	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77381974	AACATTAAAAAAAAA[A/G]GGGGGGGCCTTTAAG	78514
rs232932939	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77498280	GACTCCCCAAGAAAA[G/T]CATTACTTCTCTTCT	78514
rs232939398	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77272450	CCCTACACAAACAAC[C/T]GAGGTGCATATTTTA	78514
rs232941432	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77470020	GGCCAACGGCTGATA[C/T]TGGAAAGCACTGTTT	78514
rs232941706	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77475974	ATGGAGTAAAACTGA[A/G]CAGGACTATAGCGTA	78514
rs232955924	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77491679	GCCAGAGCTCCCGTG[C/G]CCACATTACCAGGGC	78514
rs232972263	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77373469	ACCTGGGCTAACGCA[C/T]CACAGACCTGGGCTT	78514
rs232972372	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77407228	ACTTGCTACTGTTTG[A/G]GAAGACCCATGTTGG	78514
rs232973885	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77325801	ATCACATGCAACCCT[-/C]TATTCTGAGGACATT	78514
rs232982520	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77375856	CCGCTAGTGAGGCCC[C/T]GATTTAGAGTCCACG	78514
rs232988923	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77274987	AGAGAGGCCCATTGG[C/T]TGTGCAAACTTTATA	78514
rs232990864	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77266596	AGTGAGGATTTGGTT[C/T]TATTTTTATAACTTT	78514
rs232996247	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77508683	GTTCTCTGAGGTTTT[-/G]TTTTTTTTTTTTAAA	78514
rs233001111	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77475583	TCACACACATACATG[C/T]AAACCAAACACACAC	78514
rs233001903	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77424623	TCAGAAAAGCATACA[A/C]GCTTGATTTCCTACT	78514
rs233005989	in-del	-/CA			intron-variant	Arhgap10	Mm_Celera	8:77351117	ACCAGCTACCGGCTT[-/CA]TTTCATTCCAAACTG	78514
rs233018570	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77275728	GACATTTTCAAATGT[A/G]CATGAATAGGAAGCT	78514
rs233023154	in-del	-/TCTTTC			intron-variant	Arhgap10	Mm_Celera	8:77480578	CCACACCTGGCTCTT[-/TCTTTC]TTTTTTTTTAAAGAT	78514
rs233029834	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77414552	AACTACTTCCAGAGG[G/T]TTATTTAAACAGAAA	78514
rs233030156	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77289629	CCTCTCTCTTAGTTA[C/T]ACGGCAACTTCACAT	78514
rs233038173	in-del	-/ATT			intron-variant	Arhgap10	Mm_Celera	8:77251838	TCATAACCAAAAGGA[-/ATT]ATTATTTTATACTAG	78514
rs233048892	in-del	-/GCAGCCCTCTGTGC			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503557	GCTGGCGCCTGCTGA[-/GCAGCCCTCTGTGC]GACAGAATGAGGAGC	78514
rs233049119	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77402378	CAATTCCCAGCAATC[A/C]TATGGTGGCTCACAG	78514
rs233049459	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77407704	GGTTACAGGAGCCTC[A/T]ACAGAGGGAGGAGAG	78514
rs233061435	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77323392	GAAAGAGGTTTCTGA[C/T]CCAAAGCCCAAGGGC	78514
rs233062225	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77256518	AACAATTTGCTTGCT[A/C]TATAACAACCCTCAG	78514
rs233063206	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77511555	AGGTCCCATTGTTAC[C/T]AGATGGCTTCATGTG	78514
rs233064088	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77466331	AGGTCTGTGTCGCCA[C/G]ACTTTGGGGAGATAC	78514
rs233065831	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77450581	GCTCAGAAAACCCCA[-/C]TCCCCTCAAAGCACT	78514
rs233074607	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77402712	AAAAAGAAAAAGAGT[A/G]ACTTTGTGTAGCAAG	78514
rs233086793	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77357408	AAAATGTGGATTCTC[A/G]CGCACTCATGGGAGC	78514
rs233091801	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77496354	AAAGCCCTCCTGCTA[A/G]GCTCCATCTCTGAGA	78514
rs233113104	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77309048	CTATTTTCAGATGAA[C/T]GCCTGAATCTGATCA	78514
rs233140346	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77257467	CTAAATGACAGAAGC[C/T]TCACAGACTCCTCCC	78514
rs233151093	in-del	-/CAAA			intron-variant	Arhgap10	Mm_Celera	8:77407148	GCACAGACATCTATC[-/CAAA]CAAACACTCGAAGCA	78514
rs233163949	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77509665	TCAGTTTTATTTATA[A/G]CAATGGTCACAATTC	78514
rs233173921	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77252456	TTCTTAAAGGTTCTA[C/T]CCATACATTGTAGTG	78514
rs233182765	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77378160	GCAGCGGGAACCTGG[A/C]CAAGTCTTCTTCCCC	78514
rs233185157	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77268913	TACCAGATGGATCAA[C/G]GCTGTCGCCCCACAG	78514
rs233200368	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77472181	ACATATATACATATA[C/T]ACACACACACATACA	78514
rs233207086	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77377638	GAATGCTTTCTACAC[A/G]CATGGCGCTGTGTGT	78514
rs233210701	in-del	-/AAC			intron-variant	Arhgap10	Mm_Celera	8:77466081	ATTAGAAAAAAAAAA[-/AAC]CTCCATATTGATGTC	78514
rs233229618	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77381477	CGTATTACGTCGATG[A/T]GACACTAACCTGCAC	78514
rs233230435	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77263194	TAATTCTTTCAAATG[C/T]CCTACCTACTTTCCC	78514
rs233240010	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77330765	AGACAGATGCAGGGA[A/G]TAATATAGTGGAGAT	78514
rs233244681	snp	A/G			intron-variant, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77517441	CCACCGAGGGCCAGG[A/G]TCGGGGAAAGGAACG	78514
rs233256336	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77328022	GCAGTGGTATTTTTG[A/C]GTTTTGATGTTTAGG	78514
rs233274817	in-del	-/TTC			intron-variant	Arhgap10	Mm_Celera	8:77420929	AGGACATACAGAAAA[-/TTC]GTCTTCCCAAACTCT	78514
rs233278011	in-del	-/AAGCCAG			intron-variant	Arhgap10	Mm_Celera	8:77328920	GAGGCCACATGTTAA[-/AAGCCAG]TTACCTGAGGCAGAT	78514
rs233281851	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77272435	TTGTGGGTACTGAGA[A/C]CCTACACAAACAACT	78514
rs233285732	in-del	-/A			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77502668	TAAACACTGAGAACT[-/A]AAAAAATGACCAAGT	78514
rs233288552	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77491764	AACATCAAAACGGCA[C/T]GGCCTAGGAGGCCAG	78514
rs233290488	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77372370	CCCCAGTGGGAGCTA[C/T]GAGACAGCGGCAGGC	78514
rs233293032	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77277987	ACTAACAAAGTCAGG[A/C]CAGGCCAGAGGAGCA	78514
rs233308617	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77456572	AACTTCCTAAACCTG[A/G]CCAATGTGGGTCATC	78514
rs233310411	in-del	-/AGG			intron-variant	Arhgap10	Mm_Celera	8:77290035	GTGGGAGGGGCTGGA[-/AGG]AGGAGAGGGAGGGGA	78514
rs233312393	in-del	-/CT			intron-variant	Arhgap10	GRCm38.p3	8:77506012	GAGACAGATCTGAAC[-/CT]GCCCAGGCTGGTCTC	78514
rs233321338	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77462336	TCATGTCAGCAATGG[A/G]GGGAGGGGGACTCCC	78514
rs233332740	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77363091	TAACGTGCCTGTGTC[C/T]GGACTTCTCTGAAAA	78514
rs233337678	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77353365	AATGTGTGTGTGTGC[A/G]CAGGCAGGGAGACTG	78514
rs233339461	snp	C/T			synonymous-codon	Arhgap10	Mm_Celera	8:77426366	CTTCCTGGCAGACAG[C/T]GTCAAGTGCTTGTCG	78514
rs233341653	in-del	-/GA			intron-variant	Arhgap10	Mm_Celera	8:77388381	AAAATAGGAGAAGTT[-/GA]GAGAGTTTTGCTGAC	78514
rs233348113	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77272093	CCAGGTCAGAACCAC[A/T]GCTGCTGTGGGTGCT	78514
rs233357448	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77480585	TGGCTCTTTTTTTTT[-/A]TTAAAGATTTATCTT	78514
rs233357505	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77505477	CTGTTACTTGTTTAA[A/G]AGGAATAACTGTGGT	78514
rs233358489	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77306911	TATCCCAGAAAAAGC[A/C]AGAAAGAAATTTTCT	78514
rs233368700	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77491412	TCGTCACCACAATGA[C/G]TCACTGGTCTGGTTC	78514
rs233368765	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77372774	TCTCCTTGAGCTCGC[G/T]GTGGTAAACAGTTCA	78514
rs233393958	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77345484	ATCCCTCCACAAATC[A/G]CACGCACATAGAAAA	78514
rs233396694	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77356899	ACAAAGGCTATAGGT[A/G]TAACCATTTTTCAGG	78514
rs233396734	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77425860	ACGTGAAAGCCAAAA[A/C]CAGGCCTAGCTGAGT	78514
rs233423995	in-del	-/AT			intron-variant	Arhgap10	Mm_Celera	8:77415822	GAGGTATAGCTCAGG[-/AT]ATATACAGTTTGCTT	78514
rs233440350	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77292984	CTGCTTTTTCTAACC[C/T]GTCGATCCTATCACT	78514
rs233443533	in-del	-/GG			intron-variant	Arhgap10	Mm_Celera	8:77441335	CCTCTCCCTGCATCA[-/GG]GACAGGACTAGTGAG	78514
rs233445135	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77447107	TGTTTGTTTTGGGTT[A/G]TTTTGTTTTGTTTTC	78514
rs233450324	in-del	-/AGTGAA			intron-variant	Arhgap10	Mm_Celera	8:77404180	CCCTTGGTTCTCAGG[-/AGTGAA]ATGTCTAAGCATCGG	78514
rs233455109	in-del	-/GAA			intron-variant	Arhgap10	Mm_Celera	8:77255189	GACGCAGGGCTCACA[-/GAA]GATGAGGCATCCACA	78514
rs233465896	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77480684	AGAAGAGGGAATCAG[A/G]CTCCCCAGAACTGGA	78514
rs233489095	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77335784	ATAAATGAAAAGGAA[A/G]TGACTCTGAGTTCTA	78514
rs233496416	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77446557	CAGCCTCAGCACTCA[A/G]TAGGCTGTGTGTGGC	78514
rs233497541	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77423202	GTCACTGAAGGGAGC[A/C]ATGCAACACTACCTA	78514
rs233497582	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77301072	GCTCTGGCGCTCTGG[C/T]GCTCTGGCTCCTAAA	78514
rs233499055	in-del	-/CC			intron-variant	Arhgap10	Mm_Celera	8:77443577	TGGCCTAGACACCAT[-/CC]GTTCAAAGAACACCT	78514
rs233502240	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77452483	CGCTTTTAACAACTC[C/T]GTTATTCATTTTGCA	78514
rs233528419	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77447910	GTCATACTGGGCATA[C/G]CCTGAGCATAGCAGA	78514
rs233535642	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77353395	GACACTGAAACATAT[A/G]AAAGGGGACTTATTT	78514
rs233542162	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77336327	TTTCATGTTTATCTT[C/G]TTCTACTTAGAATGT	78514
rs233544808	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77330144	TGCAGCACCAACACC[A/G]TAGGCTCCTTATGAA	78514
rs233545677	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77486540	CATGGTAGCTTCTTG[A/G]CAGGATGTGAGCAAG	78514
rs233551144	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77499534	GGAAGATCTTGTCTC[C/T]GGCCCCTCAGCTTCC	78514
rs233552251	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77271433	TGGTCCTGATGTTTG[G/T]CTATGGGGCTCTGTA	78514
rs233562222	in-del	-/GGG			intron-variant	Arhgap10	Mm_Celera	8:77466932	CGCGCACACACACAA[-/GGG]GGGGGGGGGCATTTA	78514
rs233575107	in-del	-/GGAA			intron-variant	Arhgap10	Mm_Celera	8:77435559	AGATTTAAATCTCAT[-/GGAA]GGAAGCATTTTCTCA	78514
rs233587808	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77253703	AAGTCTATATGTCAA[C/T]TTGCTTATTTCTGAG	78514
rs233588752	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77265644	GCCTGTTCTCCAGAA[A/G]CGGTCAGGCAGGGCT	78514
rs233591007	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77369228	CCCAAGTGCTGGGAT[C/T]AAAGGTGTGCGCCAC	78514
rs233609032	in-del	-/CT			intron-variant	Arhgap10	Mm_Celera	8:77292755	TGTTAGATACTCCCC[-/CT]CCCCTTTGTTCTCCC	78514
rs233609392	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77447678	CCACTCATCACCGCC[A/C]TGCTAGCATGTCAAC	78514
rs233610374	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77324016	TCCACCCCTTCCATA[A/G]GAGCATGCTCTCCCT	78514
rs233613759	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77453586	AGACAGAAAAACTAA[C/T]TGGTAAGGTCAAGCA	78514
rs233616415	snp	A/G			utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250914	GGACCCCCCACGGCC[A/G]GGAGCTACAGGAGCT	78514
rs233646121	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77464637	AAGTCAAAAGCATAG[C/T]TCCAAAGTTCCCATT	78514
rs233646433	in-del	-/ACAA			intron-variant	Arhgap10	Mm_Celera	8:77297499	CATGGATAATTGAAA[-/ACAA]ACAAACACAAAATTC	78514
rs233656000	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77444827	TCTCAAGACGGACGC[A/G]GCATTTCAGCTCAGC	78514
rs233658983	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77311206	GGATGCAGTATTAAA[A/G]CACTAAGTACCCTTT	78514
rs233682110	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77397927	ACCCACCACAGTCTA[A/T]GCTTCCTGACTGTGG	78514
rs233684697	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77428013	TATAATAAAAACTGG[C/T]AGCAAAGTCCTAGAG	78514
rs233692538	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77311776	CACGCTCCTCAGGTG[C/G]AGACAAGAAGCAAGC	78514
rs233703469	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485388	TGGGGGGCTAGCAGA[A/G]GCTCTGGGAGGAAGG	78514
rs233705269	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77412865	AAACATGAGCCACAT[A/G]AGTCACTTTTTTATA	78514
rs233706474	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77465415	CTGAGTCCCCACAGG[A/C]CTGAATCTACCTTCC	78514
rs233707710	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77347835	TTCATGTCTAACCAC[A/G]AACAACATTTTAAAG	78514
rs233724785	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77442788	ACGAGTTACGTTTAT[C/T]ATGGATATAATTCCT	78514
rs233759692	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77499430	AAATAGCCAAGACTA[C/T]ACAGAGAAACCTAAT	78514
rs233767258	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77295267	CGGCTGCTTCAGTTA[C/T]CCTAGTTCTCCTTCT	78514
rs233767897	in-del	-/CA			intron-variant	Arhgap10	Mm_Celera	8:77372344	ACAAAAGGAATGAGC[-/CA]CACACAGTGTCCCCA	78514
rs233783201	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77448128	TGCTTGGGATCCCAG[A/G]AAAGAATGACTAAAT	78514
rs233783474	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77326473	TATGTGTGTGTGTGT[A/G]CACATGTGTGTGTGT	78514
rs233787831	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77412229	TGGGGCACCACCCCA[A/G]CAAGGAATTAGCAGA	78514
rs233796760	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77471860	AGCGGAGGGCTTTAT[A/G]GACACTGTGAACGTA	78514
rs233801910	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77431758	GGGAAAAAGTTCACA[A/C]CCCAAATGCTGTGTG	78514
rs233804657	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77376244	AAAAAGGGGGCCACT[A/G]AAGAAGAAAAGAATT	78514
rs233810747	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77272919	AGCACAGACTAATGC[C/T]TTGGAAAGCCTCAGT	78514
rs233819357	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77332154	GCCGTTAGCGGACAT[C/T]CAGTTTGAAGGAAAA	78514
rs233833409	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77358650	CTGGTGAACAGCAAG[A/G]GGGGGAAAAAATTAA	78514
rs233838711	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77407893	TTTGCTATATATATT[A/T]AAAAAAAGTAGAATA	78514
rs233845424	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77273252	TGTTCAAGAAAGAAG[A/G]GTGCATGGTGAGACT	78514
rs233862083	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77431112	GATGCATGCACACAG[A/C]CGCACGCACGTGTGC	78514
rs233870884	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77471354	TGGAGGGGTCACACG[A/G]CCCCTAATGGAGGAG	78514
rs233877391	in-del	-/CTC			intron-variant	Arhgap10	Mm_Celera	8:77376633	CTGCTCCCGCCCACT[-/CTC]CTCAACCTCGCACCC	78514
rs233878851	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77468050	CCAAGTCCCTTACAG[A/T]GAGAGATGACAGGAA	78514
rs233885093	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77326386	TCTGTAATGTGATCC[A/G]ATGCCCTCTTCTGGT	78514
rs233888855	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77512209	ATGGTTCATAAAGAC[C/T]CATGGACGGCAGCTC	78514
rs233892443	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77497219	GCCAGAAGAAAGAAG[C/T]GGGCACCAGATGCCC	78514
rs233896744	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77268384	AATGAAAGCAAAAGG[-/A]AAAACCAAAGTCAGG	78514
rs233898548	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77408263	TCATTCAAATGGTGC[A/G]TGAGAGCACTAGCGA	78514
rs233906603	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77272660	CTATTTCTCTTCCCA[C/T]TCTCCTCTGTCTCTC	78514
rs233914678	in-del	-/GCTC			intron-variant	Arhgap10	Mm_Celera	8:77382658	CGAGGGCTGTGACAG[-/GCTC]GCTCGGGTGTTCCAT	78514
rs233915593	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77359077	AGCAGTTCTCTGCAG[A/G]TTAACAAGTGATCAA	78514
rs233922930	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77323020	AGAAGGAAACCTCCC[A/G]ACTGGTTCGTTCAGA	78514
rs233929136	in-del	-/G			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519183	AAGAGGCAAGGGGGA[-/G]GGAAAAACTGGAGAC	78514
rs233929633	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77447335	AGTCAAAAGCACTGT[C/T]AGCTGCCTCCAAAGC	78514
rs233930954	in-del	-/AGCCACA			intron-variant	Arhgap10	Mm_Celera	8:77354308	AGTGTCCCTCCCAAT[-/AGCCACA]AGCTACAACCCAGAG	78514
rs233941542	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77317602	AAAGCAGAACCACAC[A/C]AGAGCCACTGTCCCT	78514
rs233949238	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77400189	CTTCCCTTGACAGCC[A/G]ACAGCCTGTCCATTC	78514
rs233958779	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77472855	GAGACTCTCCCAGGT[C/G]AAAGGCCATCTAGCC	78514
rs233985156	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77452724	AGTCCAGTCATATTT[A/G]TGTGAATGCATTTAA	78514
rs233990874	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77298313	GAGGCTTGGGTGGAT[C/T]TGGGGAGGATCTGAG	78514
rs233992990	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77364947	GGATAATCTCAGCCT[C/G]CGCTGAGGACACAAC	78514
rs233995954	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77427156	TACAGCACTGAACAG[A/T]AGCCACAACGGGTCA	78514
rs233995989	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77384092	GCTGCAAGGCCAGAG[A/G]GTTTCAAGGTGTAAC	78514
rs234004416	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77496041	TTATTTTAAGAAGGA[A/G]CACTCCTAGTATCTT	78514
rs234011340	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77472468	CAACCCATTCCTGGC[C/T]CACACCCATCTGTAA	78514
rs234021796	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77252866	TCCTATAATGGGATC[C/G]TCCATTTGTCCTGTC	78514
rs234059040	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77513867	ATCATAGATGCCTTA[A/T]ACTTTTTCCCCTAGA	78514
rs234059119	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77331483	AAGAGCTACAGAGCA[C/T]GCTGTATATCTTTTT	78514
rs234069152	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77478272	CTCCCAAGTGTACAG[A/C]GAGGAGGGAAGAACA	78514
rs234079035	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77347784	TTAGAAATATAAGCC[-/AA]AGAGATAAGTTTCCT	78514
rs234080991	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77434189	ATCCTAGAAAGACCC[A/G]GAACAGACTATGTTG	78514
rs234089016	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77470884	AGAACTGGAGTTACA[C/G]ACTCTTCTGAGCTGC	78514
rs234093423	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77279349	CTTCTGCAAGGGAGC[A/G]AGCGAGCACACATTT	78514
rs234093786	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77331017	GGGGCTGTGCCACCA[A/G]GCACTGACATGTCTG	78514
rs234097920	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77407427	ATAGATAGATAGATA[G/T]AGATGGATGGATAGA	78514
rs234099764	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77403203	AAAGCAGGCAGCATC[C/G]CGGCGAAGAACCTGG	78514
rs234109584	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77515221	AACAGGCGACCTGGC[A/G]ATCTTGCCCAGTTTG	78514
rs234120416	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77274553	TGATAGCACAGTTGG[A/G]ATTTAAGAAAAGAAA	78514
rs234139101	snp	G/T			upstream-variant-2KB, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77518367	AAGGGTGCTTCGCTG[G/T]GCAAGGGCTCGCACG	78514
rs234148802	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77331865	TGTCAGCATGTGAGC[A/G]CAGGCTTCGAGACCC	78514
rs234151195	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77360618	TGTTATTGAGCCTGT[A/C]AGGCAAGGCACAGAT	78514
rs234154153	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77325147	ATCTCACTGCCTACA[A/G]ATACATTCATCAAGA	78514
rs234157658	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77270089	GAGAAAAGACAAAGA[C/T]TTCTGTCATTTCTCA	78514
rs234168935	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77259958	ATGAACAAATGGATG[G/T]ATCAAAGCTGCAAAT	78514
rs234172479	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77504843	CCTTGGAACAGAGAG[C/T]TTTACACTCTGATCT	78514
rs234172542	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77498697	CCAGGTAGGGTTTTC[C/T]TATTGGGCCCTCAAT	78514
rs234184540	in-del	-/TGTGTGTGTGTGTGTGTGTGTGTGTGTG			intron-variant	Arhgap10	Mm_Celera	8:77445954	ATAAAATATAAAGGC[-/TGTGTGTGTGTGTGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT	78514
rs234200296	in-del	-/AGAC			intron-variant	Arhgap10	Mm_Celera	8:77440476	TATGTGCTGCTGCAG[-/AGAC]AGACAGCTCAGCCAT	78514
rs234210681	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77253901	AAGAATTATTCTACT[C/T]GAACCCTTTAGTGTT	78514
rs234210736	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77260663	GTGAACGCTCGGAGC[C/T]TTGGAAGGGCTCATC	78514
rs234224520	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77452916	TAATCGGGGGCAAAA[C/T]AGCAATGCGCATAAA	78514
rs234236459	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77378605	AACTGAGAGCCAAAA[A/T]GATTTACTTATTTGT	78514
rs234262158	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77313488	AAACAGTTGTTTGTT[A/G]TAGGAGCAGTTTTGG	78514
rs234277859	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77335745	TCACTGCAGAAGTAG[C/G]AGGACCCAGATGCAA	78514
rs234278925	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77297122	AGACCTGCATGCCTC[C/T]TTTCACATATGTGTC	78514
rs234282305	in-del	-/AAGGC			intron-variant	Arhgap10	Mm_Celera	8:77424037	GCCACGTGCTGGTGG[-/AAGGC]AAGGAGGTGGAGTGT	78514
rs234288729	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77322939	CTACTACCTCATGGG[G/T]TGGGGATGGGCCTGC	78514
rs234317197	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77354216	AAGAAAATCTATTTT[-/A]TAAAAAAAGCTATAT	78514
rs234318528	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77297609	TAAAGTGACTAACAG[C/T]ATTCTGCTCTTTCCA	78514
rs234321699	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77443344	TATGGTCAGTCACGG[A/G]GAAGCCCACAGTTAA	78514
rs234321793	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77373008	GATCAAGTTGGACAG[C/G]GGTCTCCCGTGTGGA	78514
rs234322847	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77425722	AAGAAGCAAACTCAG[C/T]CTATTAACAGCAGTA	78514
rs234324677	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77374391	TGGCCCATTCAGCTG[C/T]TCACAAAGCACCTTG	78514
rs234325276	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77383741	GAAGGAGAGGAATGT[A/G]AGGGATGGAAGACTG	78514
rs234328342	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77510427	TGGCAAGTTTCCTTT[-/A]AAAAAAACCAAAAAA	78514
rs234337261	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77330037	TGCTGTCCGCTCTCC[A/G]TCTGTGTTGGCTGTC	78514
rs234338719	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77468231	CTTGTGTGGTTATGG[A/G]GAAGCTGTTGTACAT	78514
rs234339523	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77328515	CTGTCTTCCTGACTA[C/T]TTAGTTAAATGTAGT	78514
rs234343368	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77460175	AGGAGTCGGGGGTTG[A/G]GGAGCACAGGTGGGC	78514
rs234375588	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77431573	GTAAGCGGCTGTCTA[C/T]TGCTTTGATAAACAA	78514
rs234382898	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77268060	ATTAACTGTGGTGCC[-/T]TGAAAGCTTGCCAGT	78514
rs234383509	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77363423	AGAAGAAGCAGAAGA[A/G]GAGGAGGAGGAGGAG	78514
rs234385986	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77273698	GAATAATCTAAACTG[A/G]CCTTATACCTGTTAT	78514
rs234413371	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77401996	GCATCCACTAACCCC[C/T]AACTACCACCCACTC	78514
rs234413387	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77417848	CAGCCAGGGGGAGGC[A/G]CGTGCAACACACACA	78514
rs234419039	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77353948	AGAGCAGATAGAGGT[C/T]CCCTATGGATGCGGC	78514
rs234425537	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77308605	AGAGGACTTAAGAGG[G/T]TTTTTTTTCCTACTT	78514
rs234426032	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77474228	GTGGTCTGCTCCGTA[A/C]GAAGTCAGATTATTT	78514
rs234442575	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77500391	TGTGTTATTCTAAAT[A/G]GAGATATACATCCTA	78514
rs234443893	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77274054	AGAGAAAAGAGGGTC[C/T]GTGAGCTGCTTTTTC	78514
rs234448616	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77423908	GCATGGCACACAGGG[C/T]CCTGAGCAGGTGTGC	78514
rs234451452	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77268960	GCCGCATGGCTTACC[A/G]CGGCAATGGTCTCTC	78514
rs234470584	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77467131	TTTGTCTCTGCCACT[A/G]GATTACACACAGACA	78514
rs234523142	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77510294	AAATGCACATTTAAA[C/T]AAACCTTGTCTCTGA	78514
rs234543378	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77409477	CAGAGAAATCACGCT[G/T]GCCACTCATTTTCAA	78514
rs234548359	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77360097	CGCTACAAATCTGAC[A/G]GGCTTCCCACACTCA	78514
rs234549798	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77469434	ATTGGAGTCCAGGGC[A/G]TTGTGGACCCTCACG	78514
rs234559998	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77428115	CATGAAGTGTGGCTC[A/G]CTGGAAAAGAAGCAG	78514
rs234560044	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77366928	TTCTAGTTCCAACCT[A/G]TGTTTAATTCTTTTT	78514
rs234560981	snp	C/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494293	GGTGCGGTGGTGTAG[C/G]TGGTGTATGCCTGTA	78514
rs234566041	in-del	-/GG			intron-variant	Arhgap10	Mm_Celera	8:77367703	TCCTAAGGATTTTAG[-/GG]GCCCCCCCTCCCCCC	78514
rs234578890	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77372117	AGAGAAAAGCTCTCT[C/G]TTTCAGGGTGGACAG	78514
rs234585675	in-del	-/TT			intron-variant	Arhgap10	Mm_Celera	8:77398591	CTGGGGAAGTCTTCA[-/TT]TTTTGTTTTTTAAAA	78514
rs234596329	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77326963	TTTACTAAGTAGTCA[C/T]AATTTATTTCAAAGT	78514
rs234605649	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77496768	AAATGTTTGTTTGAA[A/G]CAAGGTCTCTCTCTA	78514
rs234628383	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77465000	AATACAGGAAAATAA[A/C]CCCTAAATGTTTCTG	78514
rs234633724	in-del	-/TT			intron-variant	Arhgap10	Mm_Celera	8:77360869	CTTCTAAAGGAACTC[-/TT]TTTATTTCCAGTTTC	78514
rs234643724	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77445191	CAAAAAAGATATTCA[-/G]GAAAAAAAAGGAAGG	78514
rs234653648	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77380382	AAGTTTCTCACCCTG[C/G]GGCTGGATGAAGAAT	78514
rs234657183	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77508683	GTTCTCTGAGGTTTT[G/T]TTTTTTTTTTTTAAA	78514
rs234669810	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77338265	TAAAACACCACAGTA[C/T]TGATATCCAATGTGA	78514
rs234674906	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77454906	CAGCACAACAGCCAC[A/G]GCGTGCCCTTGATGA	78514
rs234686143	snp	A/C/T			intron-variant	Arhgap10	Mm_Celera	8:77380218	TTATCAGTGCACCGT[A/C/T]ATCATGCGGTGAGCC	78514
rs234706199	in-del	-/TAGT			intron-variant	Arhgap10	Mm_Celera	8:77380145	TAGCAATACTAAAGG[-/TAGT]TAGTACGCGTGCACC	78514
rs234717045	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77380769	GCATTTAAGACTCCG[A/C]CGAGCAAGCATTCAA	78514
rs234721994	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77495196	TTGGATGCCCTGTAG[A/G]TTGGTAGAGTGTCTC	78514
rs234728144	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77281220	ACTCTCCTCTCTCAA[C/T]GAAAGCAGCATCAGT	78514
rs234741721	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77338691	AGAAAACAAAACAAA[C/T]AAACAAAAAACAGAG	78514
rs234742276	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77265899	CATCACCCTAACATT[C/T]CATGACACATGCTGC	78514
rs234743611	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77454168	TAGCATTTCGCCTCC[C/T]GGAGCAGCATCCTGA	78514
rs234758071	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77273713	ACCTTATACCTGTTA[C/T]AGACACGCTGAAATA	78514
rs234772287	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77408205	CTAAAAGCATACAGC[A/G]TCATCAGTGTCTCCA	78514
rs234775572	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77406964	GGCTGGAAACAACAA[C/T]AACACAAAACACGTA	78514
rs234785689	snp	A/C			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494423	ACACACACAGACAAC[A/C]CAGCAGACGATGGCC	78514
rs234794576	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77361967	GCCCTAGAAGGAGAG[C/T]GGTCACTCAGAGAGT	78514
rs234797264	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77253269	CGATTAGTTCCCCCT[G/T]GCTCCCTTCTCCAGT	78514
rs234800196	in-del	-/GTCACCAGCCAATAGCTG			intron-variant	Arhgap10	Mm_Celera	8:77445475	TTGGTAAATAAAGAT[-/GTCACCAGCCAATAGCTG]GGGAGGAGAGACAGA	78514
rs234815757	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77291776	TCACAGAGAGATACA[C/T]ACTACCTGCAGTCTG	78514
rs234839078	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77355575	CAGAATGCTTGGATG[C/T]ATGATCAAGTTATAC	78514
rs234842096	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77491114	AAAAACTAAGGGGCT[A/G]GAGAGATGGCTCAGC	78514
rs234845724	in-del	-/T			intron-variant	Arhgap10	GRCm38.p3	8:77441957	CTAAGCTAAGAGAGA[-/T]TTGACCTCTCCCTCT	78514
rs234851587	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77454998	AAGCTAGACACTGGT[G/T]GAAGCTGATGTAGCG	78514
rs234854331	in-del	-/TG			intron-variant	Arhgap10	GRCm38.p3	8:77283934	TGTAAGTGGCAAGAC[-/TG]TGTGTGTGTGTGTGT	78514
rs234879560	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77311064	AAAATAAAGCATCTC[A/G]TTAAAATTAAAACAC	78514
rs234883108	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77424098	CGAGAAACGTTTAGA[A/G]CAAGATGTCTAATTA	78514
rs234897908	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77450504	AGACAGAAACTTCAG[C/G]AGAGAGGTCCAGGAC	78514
rs234898209	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77255211	GCATCCACACCCTGG[C/T]GAGAGAGAGAATCAG	78514
rs234915551	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77315225	TGTGGGGCTGTGGGA[C/T]TAAGGTGGCTCTAAG	78514
rs234924022	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77415245	TCCCAGGCTGATCTA[C/T]TGTACCCGTCCCTGA	78514
rs234946819	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77378737	CATGCAGAGCAGTTG[C/T]GCTTCACCCCAAGAG	78514
rs234954641	in-del	-/AAAACC			intron-variant	Arhgap10	Mm_Celera	8:77510431	CAAGTTTCCTTTAAA[-/AAAACC]AAAAAACAAAAAACA	78514
rs234955291	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77344433	TGTGTACTCATCGCA[C/T]CTGGAGGCAAAGCTT	78514
rs234978134	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77255499	GACTAGGATGAAAAA[C/T]CTGATGCACAGAGCA	78514
rs234980171	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77321686	TTTTTACTTAATTCT[-/A]TTTTTTTTTAATGAC	78514
rs234983873	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77334372	GTCCAGGAATACAGT[A/G]GAGTCCATGGAGAGC	78514
rs234986314	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77376899	CCCCACATCAGTTGA[G/T]CACTATATGGAAACA	78514
rs234991622	snp	A/G/T			intron-variant	Arhgap10	Mm_Celera	8:77414781	TTTGTTTATTTATTT[A/G/T]TTTTTATTTATTTAT	78514
rs234996648	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77501787	CATGGCCCCTCTCCT[C/T]AAGGTGAGCAGCTTC	78514
rs235005711	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77385764	ACAAGTCTATGTAAA[C/T]GGGAAAAGTTCCACC	78514
rs235007048	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77332887	CACTATTAGGGTGTG[A/G]TTCGGTGACAATGTG	78514
rs235011687	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77279268	GCTTCAATTCTTTTT[A/C]GAATGGAGTTCCCTT	78514
rs235020324	in-del	-/CGTTT			intron-variant	Arhgap10	Mm_Celera	8:77270902	CAAAGAATCAAACTA[-/CGTTT]CAGTGGTGTGCTGGA	78514
rs235031075	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77435800	CTCAGGCAGACTCAC[-/A]ATATAAGATGTCTTA	78514
rs235049829	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77272833	ATGTAGAAATGGAGG[G/T]AAGAACAAAAGACAG	78514
rs235056065	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77435474	CCTCCAAAGGTCCAC[A/G]TGCTGAAGGGTCCAG	78514
rs235060772	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77450460	TAACACAAAGTACAA[A/G]AGCCACCCAGCCTTC	78514
rs235086806	in-del	-/TGCTGTG			intron-variant	Arhgap10	Mm_Celera	8:77325361	ACTTGGTCCGTTATT[-/TGCTGTG]TGCCATGAAGTTGAG	78514
rs235093885	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77474264	CGTTTAAGCTACTTT[G/T]CTTCTGGAAATACAA	78514
rs235098509	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77409656	CCCTGCAAATAAGCA[C/T]AATATTCAAAACTCC	78514
rs235099425	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77447069	TTAAGGGGGGGAGGG[G/T]TTGAGTGGTTGATTT	78514
rs235113404	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77488098	AACCGGCCTGGGATC[A/G]ATACAGACAAGCTCA	78514
rs235116314	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77434940	CTGAGTTTCATCAAC[A/G]CAGTGACATCTAGGC	78514
rs235116755	in-del	-/AGAGAG			intron-variant	Arhgap10	Mm_Celera	8:77511476	GAAAGAAAGGAAGAA[-/AGAGAG]AGAGAGAGAGAGAGA	78514
rs235134535	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77361451	TGCTTTATCACCTCG[A/G]ATCGTTTCCAGTTGC	78514
rs235137549	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77354051	CAGTGCTGCTTTCAT[A/G]GGAGAATAAAGACAC	78514
rs235139126	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77443739	TTAATCCCAGCACTC[A/G]GGAGGCAGAAGCAGG	78514
rs235143773	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77432129	TGGTGGGGGGGGGGG[-/AA]TGGAAATTATTTCCC	78514
rs235146693	in-del	-/TAATAG			intron-variant	Arhgap10	Mm_Celera	8:77451469	GCTTACAAAGCATAT[-/TAATAG]TAAACAATTCTCCAA	78514
rs235147378	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77352567	ATCTACAGAACTGCT[C/T]GGGCAGGGGACTGTG	78514
rs235148091	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77319827	TTGGCAGGAACCAAG[A/G]CTCTGAGAGAACCCA	78514
rs235154184	in-del	-/TAATTTAGCACTC			intron-variant	Arhgap10	Mm_Celera	8:77314458	CTATTTTCTACTCCT[-/TAATTTAGCACTC]TACCTTGTATCTTTT	78514
rs235154245	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77516923	AATACAGATGGAACT[A/G]AGGTGGCCAGCTTCG	78514
rs235160541	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77473759	TCTTTTGGTGGTGAC[C/T]TGCTCAGCTCAAGGC	78514
rs235165212	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77410055	TGCTTCATTTGGTCA[C/T]CTGGAGCCGAAAATG	78514
rs235166176	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77452460	CTGGGATTAAAGGTG[A/T]GCACCACCGCTTTTA	78514
rs235170104	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77477591	TGTAGACCAGTTTAT[C/T]TGCCTAAGCTGTGAG	78514
rs235174436	in-del	-/AT			intron-variant	Arhgap10	Mm_Celera	8:77326918	ACAATTTAAAATATG[-/AT]ATAATGTTAGCTAAA	78514
rs235178704	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77383224	AAAAGGTTTAAGAAA[A/G]GTTTTTGTTAAATGC	78514
rs235180462	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77308945	ATTACTCAGCCATTA[A/G]TAATCATTTAGAAGC	78514
rs235186811	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77495000	TCAAAACCAGTAACA[A/G]AGAAATAAATTTTCA	78514
rs235197743	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77362043	ACAGGCTTCTCCTGG[A/C]CCTGGGCTGAAGGAG	78514
rs235199382	in-del	-/AG			intron-variant	Arhgap10	Mm_Celera	8:77347864	GCTATTTGAGAAAAA[-/AG]AGAGAGATTTCCCCT	78514
rs235202214	in-del	-/AAAAA			intron-variant	Arhgap10	Mm_Celera	8:77415919	GCAGTAAAACATCTC[-/AAAAA]AAAAAAAAATATGAC	78514
rs235203806	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77254135	ATCCACCAACAGAAT[A/G]TATTTCTGGGATTCC	78514
rs235217013	in-del	-/CCCCCA			intron-variant	Arhgap10	Mm_Celera	8:77274424	GCCTCCCAGGCATCC[-/CCCCCA]CCCCCACCCTAGCAC	78514
rs235218137	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77479810	TGGTGACCACCCAAC[A/C]TTGGCCTTTCAAGTC	78514
rs235220637	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77305329	GTGGGTAGGGGAGCC[A/G]GGCTGGGGGAGGGTA	78514
rs235232642	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77339462	GAGATCCCAAGAAAG[C/G]CAGCCTAACATTAAT	78514
rs235247313	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77437506	AGACACCCTGTCACA[A/G]AACAAAGCGAAGTGG	78514
rs235253400	snp	C/T			downstream-variant-500B	Arhgap10	Mm_Celera	8:77249877	ACTCCCTTCATAGTC[C/T]AAAGGCTGCAAATAC	78514
rs235269880	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77481316	AATAGTAGCAAATGG[A/G]GACAGAAGGAAGATC	78514
rs235272519	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77475761	CACACAGATGCACAC[-/A]ACATACACAACTGAA	78514
rs235278278	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77289904	CTCAAAACAAACGGA[A/G]TCAGAGGAAAGTCAG	78514
rs235287072	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77340080	ACTGGGCAGTATGCA[C/T]ACGAATTCTGTACCT	78514
rs235290053	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77333939	CAGAATACCATGGGA[C/G]AGCACAGGCCTTCAG	78514
rs235307708	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77436842	TTCTCAGCTTCCACG[C/T]TGCAGACAGCAGTGG	78514
rs235309355	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77290621	TTTAACTTCCCTAAT[A/G]CTATGACCCTTTAAC	78514
rs235310847	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77282099	GAAGAAAAGAGACTC[A/G]CAGTTCCACTAAAAC	78514
rs235320254	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77406112	CAGGAGGCAGAGGCA[A/G]GAAAATCTCTGGGGC	78514
rs235326052	in-del	-/GTGTGTGTGTGTGT			intron-variant	Arhgap10	Mm_Celera	8:77348006	TGTGTGTCTGCCTTC[-/GTGTGTGTGTGTGT]GTGTGTGTGTGTGTG	78514
rs235336489	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77359336	TTATAAGCCATTCGC[C/T]GCCCAGAAAACTAGC	78514
rs235339556	in-del	-/G			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519177	GAAAGAAAGAGGCAA[-/G]GGGGAGGGAAAAACT	78514
rs235341586	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77334403	AGTGCAGTAGAGTTG[A/G]GAAGGAGAGTGGAGC	78514
rs235369791	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77315361	CAGGACTACGTATGG[A/G]TCTATTCTAAGGCAA	78514
rs235371488	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77258716	ACCAGCCACCGATTC[A/G]AAGTATTAAAAACAA	78514
rs235379463	in-del	-/GGAGGGCT			intron-variant	Arhgap10	Mm_Celera	8:77359681	CAAAAGATGGAAGAG[-/GGAGGGCT]GGAGGGCTGGAGGGG	78514
rs235383375	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77283220	GGAAGATGTAACTTA[C/T]TGTTGGGATTTAATT	78514
rs235389437	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77407185	CAAAAATAAACAGGG[A/G]CTGTAGAAATGACTC	78514
rs235402392	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77416556	AAAAGAAGGCAGAGG[-/A]GACAGCATGAGAGGA	78514
rs235403057	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77455479	CTTCTACTCTCAACT[C/T]CTGGAGCCCCTGTAA	78514
rs235403218	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77296411	ATACATAAAATAAAT[-/A]ATTTTTTTTTAAGAA	78514
rs235411638	in-del	-/ACAA			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77516569	CCAGGGGTGCTGTCT[-/ACAA]ACAAATGGAATAAAC	78514
rs235418792	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77363079	AGAATGACGTCCTAA[A/C]GTGCCTGTGTCCGGA	78514
rs235422585	in-del	-/AGA			intron-variant	Arhgap10	Mm_Celera	8:77460002	GTAAGGTCAAAGGGA[-/AGA]GAGCAAGACGGCTAG	78514
rs235424299	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77263369	ACTGACAGGAAACAA[A/G]GCTGGAGTACATCTT	78514
rs235428823	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77500964	TGAATGAATGGACTG[G/T]GGGATATGTGATTTG	78514
rs235429106	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77507272	AGGCAAAGAAAGAGT[A/G]ATAATCAGGATAGCC	78514
rs235431050	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77316336	ATAGGAAGCTGATAG[C/G]ATTCTTTTTTCTTTC	78514
rs235442880	in-del	-/CAAG			intron-variant	Arhgap10	Mm_Celera	8:77289047	AAACAAACAAACAAA[-/CAAG]CAAACACACACACCT	78514
rs235450104	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77428884	GAAAGAAATCAAAGG[A/G]ATATGAACATAACTG	78514
rs235450967	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77432498	GGAAAGACTTCTATC[-/T]AGAGAGGAAAACAGG	78514
rs235452416	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77263759	TGAGGACCCGGAGTC[C/T]TCTCCAATACTTCAC	78514
rs235452809	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77255769	TTAGGGAGACACAGG[C/T]GTCATGCATGGCTAT	78514
rs235478089	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77506703	CATCCGGTTTCCTCA[A/C]GTGTGACTGTTCATA	78514
rs235479328	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77309008	TAAGATATAATTTTA[C/T]TCCGAAGAATAGTAG	78514
rs235485408	in-del	-/C			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77503910	GAGAAAAACAAAGAA[-/C]CCCCCCCCCAGCAGC	78514
rs235495286	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77275775	CTTTGATTTATGAGC[A/C]AACTTCTCATGCTGT	78514
rs235496496	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77398997	GTACTGGGTTAGAAC[A/T]GTCACATTCTGGGGA	78514
rs235505550	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77418436	TCTCAGGACAGGCTT[A/G]ATGTCCTATGATATA	78514
rs235521158	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77256477	CTCTAGGAGCACACA[C/T]CGCATACAGAGTCTA	78514
rs235522594	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77462802	CTGTTTTGGAGGCCT[-/G]GCTTTTTTTTTCTCT	78514
rs235534108	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77430213	AGGTCGGTGGAATGA[A/G]TCAGTACAGTCTAGG	78514
rs235541129	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77475525	AGTTCCAGAGGACCT[G/T]GTGCCTCTTCTGAAC	78514
rs235546539	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77386367	GAACTCGGATACTAA[A/C]TCCACCTCCCAAGTG	78514
rs235557692	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77456000	AAATTTTAGAAATTA[C/T]ATTGGGTTCCAACAC	78514
rs235571311	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77470626	GTCTCTATGAGCAAA[A/G]GCCCAGCCTTTCTAG	78514
rs235574959	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77267693	CATCAAGCTGACTGT[A/G]ACAACTGCCATTACC	78514
rs235576912	in-del	-/TT			intron-variant	Arhgap10	Mm_Celera	8:77421593	GTATTTGTCTGGTAC[-/TT]TTAATTGAAAGTCTT	78514
rs235580189	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77277590	AAAAGAGGCAGAAAC[C/T]TTAAGAAGTACAACC	78514
rs235584783	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77410478	CACAGCTAGAGGCCT[A/G]CCTTCCTCACTCAGC	78514
rs235592827	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77368825	ACAGAACTCTGCCTG[G/T]TTTTTTTTTTTTTTT	78514
rs235597772	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77502982	GCATCTGGATAACAC[A/G]GTATGGACCGTCTTA	78514
rs235598942	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77434845	AAGTGCAAATTATAA[C/T]GATGCCTTCAACCAG	78514
rs235602013	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77365583	AGAGAGTTGCCATAA[A/G]CTCCATCGAAATGAA	78514
rs235615049	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77455565	GCGCTCTCAGTGTGC[A/G]GCTAGGTTATGTCAA	78514
rs235617140	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77476126	AAACACACACTATAG[A/C]ATAACCATGGGATGG	78514
rs235622369	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77411189	GACACAGTGAGAACA[C/T]ATTACTGCCCTGCTC	78514
rs235622951	in-del	-/TCTACATAATGTTGCAGAGAACATAACATGCAGGTCTA			intron-variant	Arhgap10	Mm_Celera	8:77374066	CCATTTCTTGGCTAC[lengthTooLong]TGTGGCCTGCTGGCT	78514
rs235642032	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77362187	GAATGGAGAAATGTT[A/C]TTATCTATTTTAATC	78514
rs235644157	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77447952	GACTCTCCAGTGACA[C/T]ACTTCCTCCAGCAAG	78514
rs235647815	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77502572	ACAAGCCAGGTGTGA[C/T]GTGTAAACCATTTTG	78514
rs235656781	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77262191	CTGGAAGAACAGATA[C/T]GGAAGGTACAAGCCT	78514
rs235656805	in-del	-/TAA			intron-variant	Arhgap10	Mm_Celera	8:77406745	TCACTGATAGTAAGA[-/TAA]TGACTTTCTAAATGA	78514
rs235668614	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77461060	CCATATACCTCTACA[A/T]ACATGATGTCGTGGG	78514
rs235681157	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77318248	GCTGACTAGTCTCTG[A/G]GGTCTTGTCTGGTTT	78514
rs235682855	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77406716	AGGAAAGGAATGGGC[A/G]GTGGAGAAAAAGGTT	78514
rs235682868	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77411545	ACATAGACACATGCA[C/T]ACACATGTACACACA	78514
rs235688682	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77514365	TTATTATAAGACATC[A/G]CTGAGCTCTGAAACG	78514
rs235707515	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77453722	GATCACAACTGGCCA[C/T]GTGGCATAGGGCCTA	78514
rs235726422	in-del	-/TTGTTT			intron-variant	Arhgap10	GRCm38.p3	8:77479878	TTGTTGTTGTTGTTG[-/TTGTTT]TTTTTAAATATAGCC	78514
rs235727505	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77496982	GAGGCAGAGGAAGGC[A/G]GATTTATGAGTTCAA	78514
rs235736640	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77357346	CCATGCTCCCCTTTC[A/G]GGGTCTCACTGTAGG	78514
rs235737945	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77315919	GAGCACCCATGGGTG[A/G]TATGGCAAAATGGGG	78514
rs235741141	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77340485	TGTAAATTTCCCTCA[G/T]ATCTCTCAGAACTGA	78514
rs235749605	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77381997	CCTTTAAGGAGGTGG[C/T]TAGGGTATTAGAGTA	78514
rs235751598	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77270595	TGCCCCAGCATGGAG[C/G]GAAAGGTGAGTATGA	78514
rs235764729	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77479903	TAAATATAGCCCTCC[C/G]TAATATGGCTAAATC	78514
rs235766639	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77373004	GAATGATCAAGTTGG[A/T]CAGCGGTCTCCCGTG	78514
rs235780403	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77262453	CACACACGCACACTG[-/C]CATCAGCTGCTGTTC	78514
rs235801300	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77313371	TTCTCAGAGCTAGTG[C/T]TCTGAGCAGTTAGTC	78514
rs235802304	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77337601	CTTTTCAGAGGACAG[A/G]TCTCTGCATCTCCGA	78514
rs235805253	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77329599	CCTGGTCCTTCATCT[A/T]TTTTAAATTTAATTT	78514
rs235807545	in-del	-/C			intron-variant	Arhgap10	GRCm38.p3	8:77431133	GCACGTGTGCACGCA[-/C]CCCCCCTAAACTGCA	78514
rs235808057	snp	A/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77502542	CTTTCTTCTTCCTTC[A/T]TCTTCACCATTCAAA	78514
rs235814435	in-del	-/TCTC			intron-variant	Arhgap10	Mm_Celera	8:77495207	TAGGTTGGTAGAGTG[-/TCTC]TCTCTCTCTCTCTCT	78514
rs235824128	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77382459	CCACTTGGGCCATCC[A/T]CTCTGTGGTATTTTC	78514
rs235836465	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77273342	CATACAGAGATCTAT[C/G]TAAAGCAGGAAATCT	78514
rs235837566	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77284237	GTGGCTTCTCGGGAG[C/T]GCAGTATGAAACCCT	78514
rs235854712	snp	A/C			synonymous-codon	Arhgap10	Mm_Celera	8:77409586	GCAAAACCTTCTGTC[A/C]GTGGAGTCCATGTGC	78514
rs235862719	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77452501	TATTCATTTTGCAAA[C/G]GTTCTCAGTCAGAAC	78514
rs235866802	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77364032	GATGCTGCACTCCCA[A/T]TAAATTCTTCCAGCT	78514
rs235870288	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77495519	GCTGCTGAGATTGGA[A/G]GGCAAGGTGGGTTGT	78514
rs235870545	snp	C/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485260	GCTGTCTGCTGAACG[C/G]ACTGACCCTACCCCA	78514
rs235892716	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77319725	AGGCTCTCTGTTTCT[A/G]CCTTGTTGGCCAGAA	78514
rs235901586	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77458309	ACGACTGGAACTGTG[C/T]TTGGCCTTGGACAGT	78514
rs235906191	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77357495	CACTGGCCAGTCATG[C/T]CACCTGTCACCCTTT	78514
rs235914857	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77383016	GTTTATAATTCAAAT[C/T]ATAAATAAAATTTTA	78514
rs235915098	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77285243	CCAATATATACGCGT[A/G]TGCGTGCGTGCGTGC	78514
rs235919577	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77443720	GCGTTGGTGGCGCAC[A/G]CCTTTAATCCCAGCA	78514
rs235919662	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77436452	GCTCTCAGTTCCTCC[C/T]ACCCTGGAGATCAAA	78514
rs235921628	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77346161	GCAGAGGTGTAAGCC[A/G]CTTACATAGCATCAA	78514
rs235922896	in-del	-/TT			intron-variant	Arhgap10	Mm_Celera	8:77311304	ATCCATTTGCAAACA[-/TT]TTTTTTACACATTAA	78514
rs235945739	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77313685	GCCATGTGAGATCAC[A/G]AAACAGAGTGGCCAC	78514
rs235948791	in-del	-/CAG			intron-variant	Arhgap10	Mm_Celera	8:77453798	AGGAGCTTCCCTTCC[-/CAG]ACACCCCTTCCTGCA	78514
rs235977020	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77257542	CTGAAGAGAAAATGG[C/T]GGACATGAACATCAG	78514
rs235979723	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77443306	ATAAATTCACATTCA[A/T]AAGCAACGTTCAACA	78514
rs235984638	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77497371	TTAAAAGAAAAAAAC[A/G]TCTGCATCCACAGAT	78514
rs235987720	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77285659	ATGAGAGAAAGCTGA[A/G]ACTATTTGTCGTGCT	78514
rs235990230	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77346667	TTTCTAGTAAGCTTG[C/T]AGCTCACATGGCACT	78514
rs235991230	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77416517	GTAAGGTTTATCCAT[C/T]TCAGCCATGACATCA	78514
rs236006845	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77431022	TAAAGCATAGCATAC[A/G]AGCACACTAACCAAA	78514
rs236033383	snp	G/T			utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250653	TGTGTGGACAGTGAG[G/T]TCTGCCCTCTCTCTG	78514
rs236039343	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77339693	GGTACTGCAGGCCCT[G/T]CTGGGTCCCTCCTCC	78514
rs236042510	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77446375	ATGATGATTCCATCC[A/G]ATGCTCGTGCATCAC	78514
rs236046860	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77336468	CAACCCACTAAACAA[C/T]TGAGCCTTCCAGAGA	78514
rs236059190	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77265137	AAAATTATTAGAAGC[C/G]ACTACGCCCTGTAGT	78514
rs236067857	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77282011	ATTGCAGGGAGCAAC[A/G]TGATCCTGAGATTGA	78514
rs236091123	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77257979	GGTTTCCTGTGTCAA[A/C]TTGACACAAGCTGGA	78514
rs236095031	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77452883	CAGTTTCAGAGCCTC[C/T]TACAACCCACCCACA	78514
rs236097540	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77321158	CACCACGCTGGACCG[G/T]GTCAGATAAAGGAAA	78514
rs236100131	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77327761	CCTCACGGGGTAACA[C/T]ACGCAGGCACTTCCA	78514
rs236100855	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77359000	GGATGTTGAATGGCA[A/G]CAAGTCAGTGGGAGA	78514
rs236119364	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77411362	CATGCACACACACGC[A/G]CAAATACATACACGT	78514
rs236134273	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77388596	AGAAAAATGACATGG[A/G]GATGAAGCAAGCCAG	78514
rs236149751	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77458903	CAACAGAGCAAGGCA[C/G]CCAGGGCCTAGCATT	78514
rs236156371	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77274113	CCAGCTGGGCGCTTT[C/T]TCTGCCTCTCTGAGC	78514
rs236173430	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77258499	AACTGGTCATAAGAT[A/G]TCTATGGACGTGACC	78514
rs236175787	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77308742	TTATTTTGATGACGT[-/A]AAAAAAAGTCAATAC	78514
rs236182554	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77335223	ATTGTAGGTGTCTCA[C/T]ACTCTCTCCACAATC	78514
rs236198645	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77389145	AATTCCTATTATATA[C/T]TGTATCTCTACAAAT	78514
rs236203592	in-del	-/TTTT			intron-variant	Arhgap10	Mm_Celera	8:77321686	TTTTACTTAATTCTA[-/TTTT]TTTTTTTTTAATGAC	78514
rs236237077	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77374163	TCTTGAAGCATCTCT[A/G]TGCTGTACATACCCT	78514
rs236247351	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77255586	TCTGTGTGTGTGTGT[C/G]TGTGTGTCTGTCTGT	78514
rs236262272	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77437152	TCTCCTGTGGGTCCC[C/T]GGGATCAAACTTGTA	78514
rs236265330	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77364516	TAGGCCAGGGGAGAC[-/T]TTGAAGCATCTTACA	78514
rs236278610	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77407819	GCAGTAAGAGAGCTG[C/T]CTTTCAGAATGATTT	78514
rs236279705	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77476774	CACCACATTGACTCT[A/C]CAAAGAATCACCTTT	78514
rs236299875	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77450210	CATTGCTGAGTTCAC[A/G]AGGTATGGAGCAAAG	78514
rs236312795	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77361418	GAAGAAGCAGGGAGC[A/G]CATGTGTTGTGTAAA	78514
rs236323298	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77373950	CTTTGGTGTCGGGGC[C/G]AAAGGCAAGACCACA	78514
rs236324735	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77309381	TTCCTGCTGATCAAG[C/G]TCAAAGACTGGAGTG	78514
rs236332815	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77491836	TGGACTCAGACATGC[C/T]CTCACCCCCGGCCCC	78514
rs236340196	in-del	-/TTTTT			intron-variant	Arhgap10	Mm_Celera	8:77498819	GGTCAAGAGCTCTTC[-/TTTTT]TTTTTTTTTTTTTTT	78514
rs236342552	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77476242	TATCACTTCCATAAA[A/G]CTTTAGAATATTTAT	78514
rs236343412	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77508585	TGGTCTCTTAATTGA[A/C]ATGATCTGCCTGCCT	78514
rs236346655	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77386347	ATACAAGCCAGGCTG[A/G]TCTTGAACTCGGATA	78514
rs236364761	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77264712	TCTTGTATAGGGAGA[A/T]TAAATATTCTTGCTT	78514
rs236369815	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77285353	AGAATTCGAAATAGT[A/G]CTGAGATCAGAACAG	78514
rs236375473	snp	A/C/G			intron-variant	Arhgap10	GRCm38.p3	8:77402954	CAATCCTATGAACTT[A/C/G]CAGAAGTAACATGCC	78514
rs236376867	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77342341	AGCACTTTTCATCTA[G/T]TTAGGCTGTGTCCAG	78514
rs236396960	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77455371	ACAGGCCAATACAAT[G/T]GAGGCAATGCCTTAA	78514
rs236400200	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77380864	ATGACAGGTGACTAC[A/G]AAGGCACAGAAGGGA	78514
rs236400249	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77501992	TCTCTGTCCCCGGCT[-/G]GTCCCCATGTAAGCA	78514
rs236404181	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77354762	TCCCACTGGGCCACC[C/T]ATCAGATCTGTTGGA	78514
rs236418282	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77498673	AGCCCCGCCAACTAT[A/G]CAGAGCAACCAGGTA	78514
rs236424301	in-del	-/CTCTCTCTCT			intron-variant	Arhgap10	GRCm38.p3	8:77309597	ATACAGAGTGGGCCC[-/CTCTCTCTCT]CTCTCTCTCTCTCTC	78514
rs236426188	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77342447	CTCTTCTGCCTGGAC[A/G]CAAGGACTGGCTCAC	78514
rs236439566	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77433022	GAGCTGGGGCAGCTG[C/G]GGGGAGCACGGAACC	78514
rs236445543	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77440658	ACAAGTTTTTCATCC[C/T]CAACATCCACATCAG	78514
rs236446469	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77326748	TTCCAGGTTAGATTT[A/G]CCACCTTTCCATTTT	78514
rs236448938	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77374921	GGACAGTGGTCCCTA[-/C]TTCAAGAGCCTTTTT	78514
rs236454977	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77448173	TGCGCATGCGCGCGC[A/G]CACACACACACACAC	78514
rs236458627	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77369251	TGCGCCACCACACCC[A/G]GTCATACTAGACAAT	78514
rs236465931	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77310100	AAACCACATGACCAC[A/G]AATCACCAATCGACT	78514
rs236474487	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77514973	AGAGCATCAAACTGT[C/T]GAAGCTACCTCCTGC	78514
rs236492406	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77254674	GCCACTGACTGCCAT[A/G]AACTGGTTTGTCCTT	78514
rs236492874	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77483129	AGCCTGGGCTGCCAA[A/G]ATGGCTTAGCAAGTA	78514
rs236494042	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77336576	TTAATCCAATCTCCA[A/G]TGTGAGGTACAGACA	78514
rs236494080	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77343202	GAGTCAGCCCCGGAC[A/G]TGGTTGTCACCTACT	78514
rs236504868	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77294641	GAAGCACAGGACGCA[C/G]CAGGCCTTCCTCTAG	78514
rs236512002	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77462197	CCAGGGATAGACAGA[-/C]CCCCATCTCAATGGC	78514
rs236516247	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77432907	GCAAAATGAACAACA[A/C]CACACTTGGCTGTTT	78514
rs236516307	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77362537	GAAAAATTTACAAAT[C/T]TGAAACAAACATATT	78514
rs236523531	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77400672	CAAGGGAAGTCAGTG[C/T]TCTTAACTGCTGCGC	78514
rs236537620	in-del	-/AC			intron-variant	Arhgap10	Mm_Celera	8:77448156	ATGCCAAAGGAAGTT[-/AC]GTGCGCATGCGCGCG	78514
rs236537984	in-del	-/TAT			intron-variant	Arhgap10	Mm_Celera	8:77378366	CTTCCAAGGTCTATG[-/TAT]TATTGGAGGACTGGC	78514
rs236538224	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77474805	CAGGTCAAAGGTCAC[G/T]GACTGAGGTCATGGG	78514
rs236543216	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77318427	CTTAAAATACGTAGA[C/T]CATGTATTGCTATTG	78514
rs236558263	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77333862	AAAGGATGTCAGGTG[C/T]AGAAATGGACTTTTC	78514
rs236560087	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77336952	CAAACATATTTATCA[A/G]CTAAGGAACAGGCTT	78514
rs236561608	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77416974	ACCTCCCTGCACCCC[A/G]GTGTCACAGATGTTA	78514
rs236586483	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77263305	GAGGGAAAAGTAAAC[C/T]GTGGGGCTGTTGGAG	78514
rs236587941	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77358659	GCAAGGGGGGGAAAA[-/C]AATTAAAAACCTGAC	78514
rs236588051	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77400998	GGAATAAAAGAGCTA[A/G]ATCCGACTCGAGTCT	78514
rs236590768	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77311935	GGAAAACCTGACAGT[A/G]AAAGGGGTTTAGCTG	78514
rs236599866	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77411327	GTGTCGGGACACACA[-/C]CCACACACACGTGCA	78514
rs236625981	in-del	-/AT			intron-variant	Arhgap10	Mm_Celera	8:77411610	CACACACACACACAC[-/AT]ATACACATACACACC	78514
rs236626410	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77416329	CCTGCCACCTCTGCT[A/C]TGCCATCAGAGACGC	78514
rs236630717	snp	A/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503305	ATCCTTGGAAATTTT[A/T]AAATTGTCCTTCTGA	78514
rs236631672	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77328276	TCCATATGTCTGTAC[C/T]TGACTCTTACATCTG	78514
rs236638574	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77340726	GAGCCACTAGTGTCA[C/T]GCACACCCTGTCCAC	78514
rs236647124	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77288344	GGACATTCCTCAACT[A/C]CACTTCTGAGAAAGG	78514
rs236651330	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77430951	ATCTCCACGGGAGAA[A/C]ACTTCTGTGCCTGCT	78514
rs236655373	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77291722	GCTGCCGGCTCTAAA[A/C]GAGCTAACTCACCTC	78514
rs236666975	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77272541	ATCCTGCCCCCAACC[C/T]TGAACTTTCCAGCCC	78514
rs236668476	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77509007	TATATATATACACGT[A/G]TGTGTGTGTGTGTAT	78514
rs236671395	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77319187	CGGGGAGGGTATGGG[A/G]GTCTTTTGGGATAGC	78514
rs236691566	snp	G/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77502748	TGAAGAACTGCTCGA[G/T]CAACAGGTGGGACAA	78514
rs236695155	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77284628	TCTGAGAATGTTAGG[A/G]GAGAGAGCCTAGCTG	78514
rs236695259	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77292635	AGTGAAGAAAGAACA[C/T]GCTCCGGGGGAGACG	78514
rs236697302	in-del	-/TGTCTCTCTCTCTCTCTCTC			intron-variant	Arhgap10	GRCm38.p3	8:77495206	TGTAGGTTGGTAGAG[-/TGTCTCTCTCTCTCTCTCTC]TCTCTCTCTCTCTCT	78514
rs236697683	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77335050	CAGGTTCGGAAGAGG[A/T]CTAGGTTTGGAATGC	78514
rs236699784	in-del	-/CCCTCCACTGTATGATTCCCT			intron-variant	Arhgap10	Mm_Celera	8:77421904	GCCAGAGCGGCTGGG[-/CCCTCCACTGTATGATTCCCT]CTCCAGATTCCCGAG	78514
rs236718727	in-del	-/TCTCTCTCTCTCTCTCTCTCTCTCTC			intron-variant	Arhgap10	Mm_Celera	8:77466780	GAGACATTCATTCAG[-/TCTCTCTCTCTCTCTCTCTCTCTCTC]TCTCTCTCTCTCTCT	78514
rs236738736	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77280237	AAGCTCATTTACATC[C/G]CCTCTGATCCTTTCC	78514
rs236744940	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77270580	ATGTAGCCAAGACAA[C/T]GCCCCAGCATGGAGG	78514
rs236756707	in-del	-/G			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77484561	TGACTGATGGTTTTA[-/G]GTAAGTATTTGTATC	78514
rs236765385	in-del	-/GTGCCA			intron-variant	Arhgap10	Mm_Celera	8:77270108	GTCATTTCTCAGTAC[-/GTGCCA]GTGCCAATTCTTCAG	78514
rs236766277	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77371333	ATGAATGAATGCAAT[A/G]CATAGAGTGAGAAAA	78514
rs236770017	in-del	-/AAAGAAAGAGAAAGAAAGAAAG			intron-variant	Arhgap10	Mm_Celera	8:77445287	AAGAAAGAAAGAAAG[-/AAAGAAAGAGAAAGAAAGAAAG]AGAAAGAAAGAAAGA	78514
rs236773326	in-del	-/CT			intron-variant	Arhgap10	GRCm38.p3	8:77336020	CACACACACACACAC[-/CT]ACCTACATGACACTC	78514
rs236781235	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77253831	TCTGGAAGGCCCTGA[A/T]GGGTGGTGATATCCC	78514
rs236786818	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77434010	GGCAACACACACAAG[G/T]AGAAGAAACGTCCAC	78514
rs236834862	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77271192	GAGAAGGCCAAGCCC[A/C]TTGTGGGTGGTACTA	78514
rs236835038	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77264877	CACTGTAGGCCCAAC[C/T]GACCTCATCACTGGA	78514
rs236835146	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77456336	TTTCCCATTTGACAG[C/T]ACCAGCAGCAGCACC	78514
rs236838330	in-del	-/AC			intron-variant	Arhgap10	Mm_Celera	8:77353335	TGACGCCTAAAGTCA[-/AC]CTCTGGTCAGCGTGA	78514
rs236841743	in-del	-/ATGTGGTGCCCACAGAG			intron-variant	Arhgap10	Mm_Celera	8:77405411	GAGATGCACACAGAA[-/ATGTGGTGCCCACAGAG]GCCAGAAGAAGAAGC	78514
rs236848225	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77463944	GACTATTACAAAGAA[C/T]CATCCAATTTAACCA	78514
rs236864785	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77412455	GTGTAGCCCTGGCTG[C/T]CCTGGAACTCACTCT	78514
rs236865728	in-del	-/AG			intron-variant	Arhgap10	GRCm38.p3	8:77253577	GGCACAAGAGAACAC[-/AG]AGAGCTCGGTTTCAG	78514
rs236867354	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77400113	GAAAAGAGTTTAACC[A/G]AAGCTTCCCACCAGC	78514
rs236871259	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77265277	GCAATAATCTCTCGT[A/T]GTATGGGAAATAGAC	78514
rs236871644	in-del	-/TAGA			intron-variant	Arhgap10	Mm_Celera	8:77374864	GCTGAGGCTCACATG[-/TAGA]CAGACAGTTGTCCCT	78514
rs236873504	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77499790	TTATGTTTAATATAT[C/T]AGCTTTATGTCTAAT	78514
rs236884164	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77317309	GTTCCAGAAAACAAA[C/T]CCGGAAGTAGCTGGC	78514
rs236907683	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77464496	ATTTTAGATTTAATC[-/AA]AAAAATGATTAAACT	78514
rs236919726	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77254557	CCCTGGCACACTAAC[A/G]TACTAAAGGTCCCTT	78514
rs236926550	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77418142	GTGTTGCTGTCAGCC[A/G]TGCAAGCTCTCAGCT	78514
rs236942148	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77383683	GCAAGATTCAACATC[G/T]TCATGATAAAGAGCA	78514
rs236944479	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77317998	CTGGGAGAAAGCTGG[A/C]TGAGCACAGGCATTT	78514
rs236948961	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77397980	CCTACCACTGTCTTC[C/T]ATGCCGCAAAGGACA	78514
rs236953243	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77441508	ggACGGGACACACCG[A/G]ACCTCCAGGATCTCC	78514
rs236956821	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77343522	AATCCAGAAATTCTT[C/T]CCCTAGTGCCCAGAT	78514
rs236965688	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77482571	CATGGCTTCAGCATC[C/T]TACCCCTCTGCACTT	78514
rs236985107	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77375144	TATGCACAACTCGGG[C/T]GCAAGCGATGGAAAA	78514
rs236989911	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77417802	AGAGACAAGGCAGGA[A/G]CGTGGGGCTCACACT	78514
rs236990078	snp	C/G/T			intron-variant	Arhgap10	Mm_Celera	8:77448198	ACACACACAAACATA[C/G/T]TCCTTATATAATATA	78514
rs237013144	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77384699	AAAGACGGTGCACAC[A/G]GAACCAGCAACAGCT	78514
rs237026930	in-del	-/AA			intron-variant	Arhgap10	GRCm38.p3	8:77457648	AACAATAATAATAAT[-/AA]AACTAACATACCACT	78514
rs237028786	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77481940	CAGTAGGGATGAGCG[A/C]ACGGCTTTTCAAGCA	78514
rs237039504	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77438950	AACTCAAAATCACTA[A/G]CCTAAATTCACTAAA	78514
rs237050765	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77370211	TGTTGGGGGTTGGAA[A/G]GGTTTAGAGAGGAAC	78514
rs237052325	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77410948	ATATGAAACTCAAAA[C/T]ATGATACTACTAAAA	78514
rs237061506	in-del	-/TCCGGTT			intron-variant	Arhgap10	Mm_Celera	8:77506690	TGGTTACAGGATACA[-/TCCGGTT]TCCTCAAGTGTGACT	78514
rs237066056	in-del	-/CACCTTTAGTCC			intron-variant	Arhgap10	Mm_Celera	8:77426784	GGTGGTGGTGGCACA[-/CACCTTTAGTCC]CAGCTCTGGGAGGCA	78514
rs237069996	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77266153	TGAATGCCAAGGCTC[A/G]TGCTGCCATGCTGAC	78514
rs237093308	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77488584	CATCTGCGGCCAGGG[A/G]CAGGGCTACAGAGGA	78514
rs237126989	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77367712	ATTTTAGGCCCCCCC[C/T]CCCCCCTGCAGAATT	78514
rs237137815	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77416901	CTTGTGAAATCTGAG[A/G]CTAAGCAGCACAGGT	78514
rs237142068	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77406599	GCAGCACAGACAAAG[C/T]CCCTGCAGGGGCGGC	78514
rs237151658	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77446940	TTGTTCTGGGGTGCC[C/T]GTGGCTGTCTGCTGG	78514
rs237151705	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77439681	CATGCACACATCCCA[C/T]ACATGCACACACATC	78514
rs237156938	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77323050	AAGCTGCAAGCTTTG[C/T]TCCCCAAGCATTTCA	78514
rs237164430	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77460223	GGGAAACTAAAAATG[A/T]GGGTGAAACCCAGGG	78514
rs237168281	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77359979	ACATCAAGGCACGGG[A/C]AGAATTACATGAATT	78514
rs237176633	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77320529	CATAAGCAGGTCTGC[C/T]TAGAGTCTAGACACA	78514
rs237189860	in-del	-/TT			intron-variant	Arhgap10	Mm_Celera	8:77487120	AAAAAAAAAAATCAA[-/TT]TTTTTTTTAAATGCT	78514
rs237189926	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77429445	CCAGTGAGCATGCGC[A/T]CACAGCACAAGTGTG	78514
rs237191499	snp	A/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503223	TGTTCTAAAAATAAT[A/T]GGGACTGTCTAATAT	78514
rs237195332	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77361374	CTAGCCACCACAGAC[G/T]TGGGCCATTTTCTTT	78514
rs237200288	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77412990	TGGTTTCTATAACCA[C/T]CCACGGTATTCCTAG	78514
rs237215528	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77317117	TTGTTCACTTTTTCT[C/T]GGAACCGGAAGCATC	78514
rs237217147	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77472406	TCAGTGGTTAAGAGG[C/T]TAATAGCACTGGCTA	78514
rs237220381	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77446448	ACCAATGTGGTTAAA[C/T]TGCGCTGGCCTTGCA	78514
rs237223838	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77396367	ATTATAGTCAACAAC[A/G]CAGTGGTAAGAAACC	78514
rs237224386	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77342088	TGTGATGACCAAACC[C/G]TCACCAAAGAAGCCC	78514
rs237224831	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77315839	TAATGGTAAGAGAAC[G/T]TAAAGTATACAAGAG	78514
rs237226385	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77350607	CAAGAAGGTAACAGT[C/T]AGAGCCATGTTCAAG	78514
rs237240356	in-del	-/AAG			intron-variant	Arhgap10	Mm_Celera	8:77299977	CAAAGAAGAAGAAGA[-/AAG]AAGAAGACGAAGAAG	78514
rs237242863	snp	A/C			missense, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77517642	TACTTTTGGTGGCAG[A/C]GATGAGGTTCTTGCC	78514
rs237255852	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77260757	GGTTTGTTACCAAGG[C/T]CCATCAGGGCAGGAA	78514
rs237256790	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77437038	TCCCAGGGAGTGTGC[C/T]TTTCGTTATTAAATT	78514
rs237257976	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77353515	CAAGTATGACGAACC[A/G]CTCATACACCAGGAA	78514
rs237265514	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77259861	TAATAAATAAATCTT[A/T]AAAAAAAAAGCTAAT	78514
rs237274184	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77478008	GGCCTCACAGGCCTG[C/T]GTCCGTCGACACCAA	78514
rs237284185	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77307452	AAACAGAAACTAAAC[A/G]GTGACACATGGAAAC	78514
rs237285681	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77396785	CCAATCATGCATCAC[A/G]GTGAGCCTTGCTAAA	78514
rs237286723	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77342783	GCAGGACCATAAATG[A/G]AGGCATAAGTTCACC	78514
rs237303936	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77478183	CAGGACTCATTTTCT[C/T]ATTCTTACCAAAACA	78514
rs237316239	in-del	-/AAGTTTATCCACT			intron-variant	Arhgap10	Mm_Celera	8:77409849	TACTGCTGGGATCAC[-/AAGTTTATCCACT]AACACAGAACCACTG	78514
rs237317600	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77339331	CCATCACACCGAGAA[G/T]TCAAAATAAGACATT	78514
rs237323211	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77338215	TATGCAAAGCTCCAC[A/G]GATATTAATTGTGAG	78514
rs237325572	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77501896	CTTAGCCTGGCACGG[C/T]TGGACAGAGATAAAA	78514
rs237328549	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77285138	GATGCTGAGGCAGGC[C/T]GATCTCCATGAATTC	78514
rs237336464	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77376426	CAAGGTGTCAATTGT[A/G]GCGATGACTACGCTG	78514
rs237350437	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77470943	TCCTCTGGAAAAGCA[A/G]CCAGTGCTTTTGTTT	78514
rs237358113	in-del	-/CGTGTGCACGCAC			intron-variant	Arhgap10	Mm_Celera	8:77431121	ACACAGACGCACGCA[-/CGTGTGCACGCAC]CCCCCCTAAACTGCA	78514
rs237363221	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77332276	GTTCATGCTGCTTGC[A/C]TAAAACGATTCAGAT	78514
rs237365175	in-del	-/AAC			intron-variant	Arhgap10	Mm_Celera	8:77406746	CACTGATAGTAAGAT[-/AAC]GACTTTCTAAATGAC	78514
rs237373477	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77294015	GACAACCACTTAGTG[C/T]TCTTCTCATTCTCCT	78514
rs237376664	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77435442	TAAGAGCACTCCTAC[A/G]GTCTGGATCTAAACA	78514
rs237379879	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77369766	TCCCACATAGCACGA[-/C]CTGTCCCACAGTCTG	78514
rs237380528	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77330202	TCCAACACATGTAAA[A/G]CATAAGAACTTGAGA	78514
rs237380565	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77323965	GGGCCCATTGCTTAC[C/T]GTAGGAAAAAGACTC	78514
rs237385335	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77276406	AGTAATGTGAAGAAC[A/G]CTTTCCAATCCATTT	78514
rs237391210	snp	C/T			intron-variant, missense	Arhgap10	Mm_Celera	8:77476608	CAACTGTGGGCTCCA[C/T]AGCACACTCTCAACA	78514
rs237393824	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77329704	AGCTTTTGGAAGACT[-/A]AAAAGATGGCTCCGC	78514
rs237408227	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77411343	CCACACACACGTGCA[A/C]ACGCATGCACACACA	78514
rs237420582	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77469689	ATGGAACCCTCTTCC[A/G]GCCCCCATCGGCACC	78514
rs237426064	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77286956	TATTAGGAAATAAGA[A/G]CATTTTATGCCAACA	78514
rs237447038	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77257941	AGGCGCAACAATAGG[A/G]AATGATAGAAGCTGT	78514
rs237452866	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77366575	CTCACTGTTATGGAC[A/C]GACTAGCTGGGCAGA	78514
rs237455432	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77454162	CTCAGCTAGCATTTC[A/G]CCTCCCGGAGCAGCA	78514
rs237456712	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77384255	AGCAACCAGAGGTTC[A/C]CCATCAGGCTGGGGC	78514
rs237462702	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77443848	CTCGAAAAACCAAAA[A/G]AAAAAAAAAAAAAAA	78514
rs237463034	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77324280	GAACAAAGCAGCCAC[A/C]AAGCTTCACAGTAAA	78514
rs237465854	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77497309	CTCTGCTACAGCAGC[A/C]GGTGCCTTTAACTGC	78514
rs237483046	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77323394	AAGAGGTTTCTGACC[A/C]AAAGCCCAAGGGCTA	78514
rs237497092	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77253046	CTTTGGGCTATTTTT[G/T]AGTACTGCTGCTGCT	78514
rs237501665	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77265857	AGCCCAGCTTGTCTA[C/T]GTTAGCTCATTCGCT	78514
rs237514294	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77510952	ACCTGTGCACTTGAC[C/T]TTGATTTCTACAACT	78514
rs237522477	in-del	-/TGATAGTG			intron-variant	Arhgap10	Mm_Celera	8:77468346	ATTACTTCGGTCTGT[-/TGATAGTG]CTCTATGGAGAGCAG	78514
rs237524553	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77442253	CCAACCCCCACCCTG[A/G]CCAAGAAGAGGTGAG	78514
rs237527425	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77325384	CCATGAAGTTGAGGC[-/T]TTTTTTCCCTGACTG	78514
rs237532416	in-del	-/TAATAGCTAAGAAAT			intron-variant	Arhgap10	Mm_Celera	8:77448318	ATATTTACTCTTCAC[-/TAATAGCTAAGAAAT]TAGTGACTATAACAT	78514
rs237541733	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77434368	GTAGAAGCGAATTGA[-/C]CCCCTCGACCAGGTT	78514
rs237557638	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77382364	TTCCATCTACAAGCC[A/G]AGGGCACAGGCTAAG	78514
rs237559038	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77315709	CTCACAGAGACAACG[G/T]ATTTGGAGAAAGCCA	78514
rs237564709	in-del	-/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484499	GTAGCTCATTTTGAG[-/T]TTAGGTAAGACTATT	78514
rs237565206	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77510216	AACCTGTGTCCTCTG[C/T]GAAAGTAACATTGTA	78514
rs237568581	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77440342	TGAAGGGCTCATGCT[A/G]ATGTGGTCCCTTAGA	78514
rs237599006	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77259738	TTCAAATCCCAGCAC[C/T]CACATGGTGGCTCAC	78514
rs237601028	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77345164	AGATGTGTGTCACAG[A/G]AATGGAAGGCTAACA	78514
rs237604461	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77266169	TGCTGCCATGCTGAC[C/T]GTGGGCTTGTGTGTG	78514
rs237611045	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77292265	GTGCCACCGCAGCTA[A/T]GGCCAACCCCAGACA	78514
rs237627738	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77417136	GCTTCCTGATAATCC[C/T]GACACCCCTCCTGCT	78514
rs237630321	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77401777	ACAATATAATTCTAC[A/G]AACATTCATGGGCAT	78514
rs237641654	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77260174	CCGCCTTTACCCATT[A/T]CTCCTCCTCAGAGAG	78514
rs237648736	in-del	-/ACCACCCCCCCCCA			intron-variant	Arhgap10	GRCm38.p3	8:77506069	CTTGAACTTGTGACC[-/ACCACCCCCCCCCA]CCCCCCCCCCCGCCT	78514
rs237663960	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77338314	ACCGCTAGAATACCC[A/G]TATACCTGATCAATG	78514
rs237667271	in-del	-/AGAAATACACACACACA			intron-variant	Arhgap10	GRCm38.p3	8:77467662	ATTACTACAGAAATT[-/AGAAATACACACACACA]CACACACACACACAC	78514
rs237674493	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77288520	TTGTACAACAAAGTC[A/G]GGAGACCCCCTCACT	78514
rs237681742	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77410033	ACATCACAGCTATAC[C/T]CTACACTGCTTCATT	78514
rs237696383	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77285258	GTGCGTGCGTGCGTG[C/T]GTGTGTGTGTATACC	78514
rs237699493	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77451996	GTTTCCAAGATAAAA[C/G]TCTTGCACGTGGATA	78514
rs237706900	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77511273	GGAGAGATGGCTCAG[C/T]GGTTAAGAGCACTGA	78514
rs237711048	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77325979	GCTCACTGCTCTTCT[G/T]TTCTGTATCTCCATT	78514
rs237723491	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77364724	ACGAATCCCCGAGAC[A/G]CAGGCCCTCCCTGAC	78514
rs237743089	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77464593	GCACAGGTTTCCCCT[A/G]TGAATTCCCTGGTAT	78514
rs237743736	snp	G/T			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519530	GGGGGGGAGGGAGGG[G/T]TAGGTGGCATGGCTT	78514
rs237746554	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77508990	AGACTTTCTTAATTT[A/C]ATATATATATACACG	78514
rs237755674	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77269738	CCAAAACAAACAAAC[-/AA]AAAAAAATCAATGAA	78514
rs237755842	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77320167	CAGCACTTGGGAGGC[A/C]GAGGCAGATGGATCT	78514
rs237759508	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77405223	CCTCATAGCCTTCTG[G/T]GCCAGAAACCCGGGG	78514
rs237768288	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77329785	ACATGGTAGCTCACA[A/G]TCATCTGTAACTCCA	78514
rs237770132	in-del	-/ACAG			intron-variant	Arhgap10	Mm_Celera	8:77434159	ACGCTGAAGAAGAGA[-/ACAG]ACAAAGAACTAGTCA	78514
rs237783446	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77435778	GATGAAGACCTCAAA[A/C]CCCAGACTCAGGCAG	78514
rs237788492	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77265219	GTGCGTGGTTCTCAC[A/C]ACCTCACTTGCAAGG	78514
rs237794517	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77463871	CTCCACCCACCGCTT[-/A]GCAGGGGCCTGGCGT	78514
rs237797535	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77500527	AACATTTGACTGATA[C/T]AGTTCATGGTGTATT	78514
rs237802049	snp	C/T			intron-variant, downstream-variant-500B	Arhgap10	Mm_Celera	8:77358186	TACGCCCTAGTCCCC[C/T]CATCTCCCTCTCCTC	78514
rs237812214	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77372088	GCTGCCCTTACTTTC[C/T]ATTCATACAAAACAG	78514
rs237816762	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77427059	ACAACCCTAAGACCT[C/T]CCAGGGAAGTCATCG	78514
rs237822838	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77309584	ACACACACACACACA[C/T]ACAGAGTGGGCCCCT	78514
rs237849300	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77442294	AAGTTACAAACAGCT[C/G]AAGCCAAAAGACAGA	78514
rs237877139	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77365913	TTGAACCAGGACTTA[A/G]GAACTGGGAGCTGGG	78514
rs237878479	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77258044	CGCCTCCATGAGATC[C/T]AGCTATAAGGCATTT	78514
rs237882010	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77397847	TGGAACCGAAACGTT[C/T]GGCAGCACCACTGCT	78514
rs237896331	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77381259	AGGAACATAGTTCAC[A/T]AGATGAATCCTCTTG	78514
rs237903743	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77475596	TGCAAACCAAACACA[C/G]ACAGGCATAAAATAA	78514
rs237905298	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77476801	CTTTGCACCAGATTG[C/T]TCACCTTTTTGCTGT	78514
rs237913812	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77418743	AGCGGTTCTCAGCCT[A/G]TAGGCCACCACTCCA	78514
rs237917899	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77261381	GTCCCAGGCGTGAGT[-/C]CACGCCAGAGCGCAG	78514
rs237919087	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77352453	TGCATTATGCAAACA[A/G]TAGCATGATGCTGAG	78514
rs237923730	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77322264	GCCTGCAGAAATGAA[C/G]ATGTCTTCAAAAGCA	78514
rs237938060	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77490232	AGGGGCTTAGCCAGC[C/T]CCACCCTACGCCTGC	78514
rs237938691	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77283469	TTATATGGAAATCTT[A/C]CTCTCTTCCACATAT	78514
rs237944670	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77398140	TCCCGTGATGGCACT[A/T]CTTCTTTTTTTCTTT	78514
rs237945042	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77336788	CCAGCACACTTGAGG[C/T]GGGCAGGGAAAGAGA	78514
rs237948821	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77294885	CAGATGATTCTAAAT[C/T]GTATTTTTAACTTGC	78514
rs237961144	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77460261	AGCAGAGGATCCACG[A/G]TATACAGCCTCAGCA	78514
rs237973762	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77424966	TGTGTGTGTTCTCAA[C/T]GATAAAGAACTATTT	78514
rs237974785	in-del	-/GACA			intron-variant	Arhgap10	Mm_Celera	8:77420446	CTGTAACAGAGTGGG[-/GACA]GACAGGGGTCACGGT	78514
rs237981738	snp	C/T			synonymous-codon	Arhgap10	Mm_Celera	8:77344751	TGGTCCAAACACCAC[C/T]CCTAAATTCGCCACT	78514
rs237985672	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77295735	TCATATATGACAAAA[A/G]TTGTTTTCAATTGCT	78514
rs237990463	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77283010	CCTTCACTCAGCCTC[A/G]AATGTGGTCACGACA	78514
rs238011258	in-del	-/GGTGG			intron-variant	Arhgap10	Mm_Celera	8:77334032	AAGTACCAGAAAAGT[-/GGTGG]GGTGGGGTGGGGTGG	78514
rs238016789	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77465429	GCCTGAATCTACCTT[C/G]CCCTACTGAGAAACA	78514
rs238021206	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77459922	TGCCCCCTGGGCCAC[G/T]CAAGTGTGGATGACA	78514
rs238029686	in-del	-/CGT			intron-variant	Arhgap10	Mm_Celera	8:77322097	CGCTTCCACAGCCAA[-/CGT]CGTGCCACACCATCT	78514
rs238036230	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77272601	TCTTCTCTAGATAAT[A/C]CATATGGTTTCATCT	78514
rs238039952	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77345187	GGCTAACATCACTGC[A/G]GACCTTGCCAGACTG	78514
rs238040796	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77452822	CCAAGGGACAAGGGT[A/T]CACTTCCCAGTCTCT	78514
rs238042705	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77274906	ATGAACTAACCAGTA[A/C]CTCCCAGAGCTCGTG	78514
rs238056860	in-del	-/TAGATAGATAGA			intron-variant	Arhgap10	GRCm38.p3	8:77407328	GGCCTCCATTTACTT[-/TAGATAGATAGA]TAGATAGATAGATAG	78514
rs238071515	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77440715	GTTTCGGAGGACCCA[G/T]CGCCCCCTGCTGGCC	78514
rs238075910	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77358653	TGAACAGCAAGGGGG[-/AA]GGAAAAAATTAAAAA	78514
rs238077080	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77496173	CACGACATGTTATTT[A/T]CAAAGGTTTGCCTGC	78514
rs238078712	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77464966	CCTTACCTAGAAAAC[A/C]GGTACGTAAGATTAC	78514
rs238091783	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77407469	GACAGACAGACAGAC[A/T]AATTAATTCATTTAT	78514
rs238103854	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77460260	TAGCAGAGGATCCAC[C/G]GTATACAGCCTCAGC	78514
rs238105992	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77481424	GGGAAGAAATTATAT[C/T]TTGATGGCTTTGCCT	78514
rs238112201	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77325637	GATATTTACAAATCT[A/G]CCTCACTCTTTTTTA	78514
rs238122700	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77266862	TTTACCACAGGGATT[C/T]CCACTTGCCTTCTTC	78514
rs238123865	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77272955	GTTCTCATCTTTCTC[C/T]AGAAGGAAGGAGGAT	78514
rs238132004	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77414980	TCCTCCATGTCACCA[C/T]CTGCAGCATCTCCCA	78514
rs238134495	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77466842	CTCCTCCCTTTGCTT[G/T]AGGCATGGATTTTAT	78514
rs238137422	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77439347	CAATGAGCGTTTCAC[A/G]GTTATTAGTCCAACT	78514
rs238143376	in-del	-/CCAAAC			intron-variant	Arhgap10	Mm_Celera	8:77338854	TGACCAAAACCAAAA[-/CCAAAC]CCAAACCAACTCGGA	78514
rs238153143	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77402607	GACCCTGTATCAGAA[A/G]AGGTCTGGAGACTGT	78514
rs238155902	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77415351	AGTGTGCTCACAGCC[A/G]CTGCTCCATCTCAGA	78514
rs238163673	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77480330	CTGAGTCCATGAAGC[A/T]CTCTGTCCATCTTTG	78514
rs238168886	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77399747	CCTGACAACTGAGGC[A/G]CCGTGTCCTCAGTCC	78514
rs238176336	in-del	-/GCTC			intron-variant	Arhgap10	Mm_Celera	8:77489594	CTGTAACTTCTAGGT[-/GCTC]GCTCTCATGCTACAA	78514
rs238177127	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77319966	AATGAATTCTGCCTT[C/T]CCTTATTCATTTACT	78514
rs238178511	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77385846	CAGTAATGTCTAGTC[C/T]ACTGCTTCCTGTTTC	78514
rs238178577	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77293020	ATGAGTTAAAAAAAC[-/A]AAATCATTGGTCTAC	78514
rs238182158	in-del	-/TCTCTGTGTGTGTG			intron-variant	Arhgap10	Mm_Celera	8:77255572	CTGTGCACGAGTCTC[-/TCTCTGTGTGTGTG]TGTGTGTGTGTGTGT	78514
rs238182472	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77459003	GGCAAATGCGTGGGC[C/T]AATTCATTCCCTCCT	78514
rs238185003	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77312542	GACAGCAAGGTGCAG[A/G]TGCCAGCCATCCTTG	78514
rs238196458	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77421144	CATGAACAGCTATAA[C/T]GCCAGCACTTGGGAA	78514
rs238196762	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77414479	AAGCAAAATGCTGGC[A/G]CCCTGGTTCCTTCCT	78514
rs238199599	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77466032	CAAAAAGATATTTTC[A/G]AGGTGTGGGGATGCT	78514
rs238199954	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77472546	ACTCATTCATTCATT[A/C]AATAAATAAATAAAT	78514
rs238209063	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77501870	TCACCTGCACCAAAT[A/G]CTGGTGAGGTCTTAG	78514
rs238221590	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77341865	AGGCCCCATGTAGGC[C/T]ACGCAGCCCTGTTAA	78514
rs238225707	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77256300	TGCTGTTCCAACACA[C/T]GACAAGGTGGCTGTG	78514
rs238241492	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77506966	GCCACAGGTCCAAAG[C/T]AAGAAGCCTAGGGAC	78514
rs238250274	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77464393	GTGTGGACATTCTTT[A/G]AAGTAGAATGAGAAG	78514
rs238253102	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485106	CAGTCACTCACTTCT[A/G]TAAGGAACTAACAGC	78514
rs238260039	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77420540	CGGTTTAGATGTTTC[C/T]CTAGACTTTCCCTAG	78514
rs238261202	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77343258	TGCTTCGTCCCAGGA[C/T]CTGCTACAGGCTTAG	78514
rs238262304	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77374719	GCTCACATGCAGACA[A/G]TTGTCCCTACTGCAA	78514
rs238267351	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77378060	AGCCTGCTCCACTAT[A/C]CTCCTGCCCTGCCTG	78514
rs238270151	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77507318	CGAGGACCCTGCTCC[C/T]CACACACTCATCATA	78514
rs238297490	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77290686	TAAAATTATTTCATC[A/G]CTATTTCTCAACTGT	78514
rs238311442	snp	C/T			intron-variant, missense	Arhgap10	GRCm38.p3	8:77491983	TCATAGAGTCGTCCA[C/T]TGCCACGGGGTGGCT	78514
rs238313762	in-del	-/ACACAGACACACACACACAC			intron-variant	Arhgap10	GRCm38.p3	8:77377822	CACACACAGACACAG[-/ACACAGACACACACACACAC]ACACACACACACACA	78514
rs238316284	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77441738	ATCTGTTCCCCACCC[C/T]CCCCCCCCACACACA	78514
rs238319224	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77288725	TACAGCCGCCCATAT[A/G]TTCATCAGACTGAAA	78514
rs238348403	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77370065	GCACTAAACTGGTGA[G/T]CGATGATGAACAGGA	78514
rs238357507	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77420197	ACAAAGGAGAGGAGC[A/G]TTAGTTAGTGCATGC	78514
rs238359703	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77491658	CCGCAGCAGGCAAGG[A/G]GTATGGCCAGAGCTC	78514
rs238362617	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77290807	AGAAGCACAGGTGTG[A/G]CAGCAAGGCTGCTAA	78514
rs238374574	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77324757	ACTGAAGAAAAAAAA[A/T]TCTAAGTTTACTACA	78514
rs238376875	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77372946	AGTCCCACCTGCAGG[A/G]AGGAGGAGGTTGCTG	78514
rs238380900	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77408401	GCTGGGCCCTGTAAC[A/G]CAGTAGTTTTAAAAG	78514
rs238383273	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77447725	CTGACGTGTGTCTTC[A/G]TGAGAAGACGCATCG	78514
rs238383528	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77272254	GCAGCTGGGTTTCAT[G/T]CTTCAGGAACTGGGA	78514
rs238384961	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77441087	AGAAAGGCTTCCCAA[A/G]GGGCTGACGGTTAGA	78514
rs238387810	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77269688	TCTTTTTAAACTTAC[A/G]TAACATCCTTGCCCT	78514
rs238389766	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77462991	GCGACTAGACAAATC[A/G]GCATGTTTTAATGGA	78514
rs238409839	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77448362	TTATACAAACACTAG[C/T]TGAACCTGTCAGTGC	78514
rs238413323	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77506054	ATAGACAAGGGTGAT[C/T]TTGAACTTGTGACCA	78514
rs238435200	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77319328	AGTTCCAGAATCAAC[A/G]CTGTCACCATTGAGG	78514
rs238440723	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77360196	TCAGCTAGAACCAAA[A/G]AACTAGCTGTCTCCA	78514
rs238445421	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77447314	CCTCATTCCCTCATT[C/G]GCCTCAGTCAAAAGC	78514
rs238457517	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77513164	CCCCAGAAAATGGAT[C/T]TAGCTAAGCAGGGCT	78514
rs238470922	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77448039	TATGGGAGCCATACA[C/T]ACTCAAGCCACAGCT	78514
rs238472415	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77317706	ATGTATGGCAACAGT[A/G]TTTCCTTCTTTACCA	78514
rs238473726	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77415438	GCATACAGTCTTATG[C/T]ACATACTCACATTCT	78514
rs238474158	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77263801	GGTCCCTGCTCTACC[A/C]CTGCAGACATGGAAC	78514
rs238488506	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77262889	CAGGAAAGAGCTTGA[A/G]GCTCTTGGAGAATAG	78514
rs238501752	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77404814	ACAGGGATTCTCTGT[A/G]TAGCCCTGGCTGTCC	78514
rs238502874	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77353780	CACAGAGCCATTTAA[A/G]CAGTTTTGTGTACAG	78514
rs238517664	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77341770	CACTACTTTCCAGTC[C/T]AATGGAGGCATGTGG	78514
rs238522553	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77264039	CTGGGAACTCTAGGA[A/T]TGGCCATCCCAGTCA	78514
rs238524113	in-del	-/AC			intron-variant	Arhgap10	Mm_Celera	8:77264668	CACACACACACACAG[-/AC]ACACACACAGAGAGA	78514
rs238533532	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77296593	AAGCACAAGTACTCT[C/T]GCTCATTTTAATCTT	78514
rs238542618	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77453827	TGCAGGAGGTGTTTA[A/C]TCTCTGTTCACCCTG	78514
rs238542934	in-del	-/ATGCACACAA			intron-variant	Arhgap10	Mm_Celera	8:77411375	CGCAAATACATACAC[-/ATGCACACAA]GTGCACACACAGACA	78514
rs238543534	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77288786	TGACGCTTACGATGC[A/G]ATGCGCTGTCAAGAG	78514
rs238546800	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77399226	AATTCATAATGGTAG[C/T]AAAATTACAGTCATG	78514
rs238565342	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77488154	TAGCCAGCCAGCAGG[A/G]AAGAGAAGCTCCTGA	78514
rs238577482	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77486464	AGATCTGTTTGCATT[C/T]GCATCCTGAATGCTG	78514
rs238580265	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77253999	CACTACACATGGAAA[C/G]CAACCAATACATCGG	78514
rs238593509	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77431883	TTTGTGCTTTGTGTC[C/T]CTCACATACAAGAGA	78514
rs238614783	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77297238	TCACCTTTAAGGTAA[C/T]ATAAAAATCACCCAA	78514
rs238627270	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77326167	CCACATGGTGGCTCA[A/C]AAACATCTGTAATGA	78514
rs238636340	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493986	GTGTCTAATCTGTGC[A/G]CTCAATAAGTGATGG	78514
rs238637391	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77323957	AACATGAGGGCCCAT[-/C]TGCTTACTGTAGGAA	78514
rs238661026	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77472115	ATCGTTTGCTAAAGA[C/T]GATTTTATATATACA	78514
rs238664430	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77334436	CGCGGAGAGAGAGAG[A/G]AGGAGGCAGTTTCAC	78514
rs238685142	in-del	-/GAAGATAGAAGAA			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493273	GAGGAGGAGGAGGAG[-/GAAGATAGAAGAA]GAGGAGGAGGAGGAG	78514
rs238687688	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77513922	CTGAAAGAGGACACT[A/G]GTTATTCTACAGAGT	78514
rs238691824	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77326722	ACCTGTGAATATAAA[C/T]AGCTTCCCCCTTCCA	78514
rs238691911	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77368676	TGATCACCTCACGCT[-/C]CCAACCTTCCCATGT	78514
rs238692721	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77414152	TAAGGTCCCACGGGC[A/G]GATAATGTCCAGGCA	78514
rs238697901	in-del	-/A			intron-variant	Arhgap10	GRCm38.p3	8:77464941	AATAGATCTTTTTTT[-/A]AAAAAAGTGCCTTAC	78514
rs238701524	in-del	-/CAGAGGAACGGCAGAA			intron-variant	Arhgap10	Mm_Celera	8:77295229	GCGTGGATATGAACT[-/CAGAGGAACGGCAGAA]CAGAGACAGCCTATC	78514
rs238702541	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77268652	TATGGCCCCCAAGGT[C/T]TCTGTGTAGACATTT	78514
rs238712711	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77262787	ACACATATGCAGGCC[A/G]CTCTCATTTAAACTT	78514
rs238715368	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77506418	CATTCTCTGCCTTCC[G/T]TCCACGTCATGCATT	78514
rs238723534	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77369584	ACATGAATGCTCACT[A/G]GTGCACAGTAGTAAT	78514
rs238763388	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77443281	TCAAGTGGTTTATAC[C/T]ATTTATGGTATAAAT	78514
rs238764954	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77404120	AGCAAAGGGCACAGT[A/G]AGACTGGCCTGTGGC	78514
rs238766257	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77430251	ACTGACTCTTACACA[C/G]TGCTGCTACTCACAC	78514
rs238773693	in-del	-/ACTA			intron-variant	Arhgap10	Mm_Celera	8:77429044	CTTTCAGATGTAAAC[-/ACTA]ACTAACATCCATGTT	78514
rs238799962	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77269063	GAGAGTCCCACAAGC[A/G]ACTAGACAGGTCAGA	78514
rs238812773	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77353909	TTGAAGTAGCCACGG[-/AA]AACAGTTCCACTTAT	78514
rs238818673	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77426157	AGAGCCTAACATTCA[C/T]TCTTATCAATCAATA	78514
rs238821281	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77514724	TTGTTTGTTTGTTTG[C/T]TTGTTTAAAATAGGG	78514
rs238821561	in-del	-/AAC			intron-variant	Arhgap10	Mm_Celera	8:77286915	ACAGTTAAAAAAAAA[-/AAC]CCAAAATAACAATAG	78514
rs238824000	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77398490	TGTCTTTTTAAATAC[C/T]GTAATCTTCCTGTCT	78514
rs238835413	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77263520	CCCATGTACCTAATG[G/T]AACCATCTCTGCTCT	78514
rs238837259	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77437550	CTTGGAGACACATGG[A/G]AAAACCCCTCAGGGC	78514
rs238839256	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77433434	cacacacacacacac[A/C]cacacacacacacac	78514
rs238845878	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77427413	GTCTATCAACGTCCC[A/G]GTCCCCCCTGCTCTT	78514
rs238860923	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77368658	TCTCAGCTGCCAAGA[C/T]CACTGATCACCTCAC	78514
rs238870586	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77491948	CATTCCCCCCCAGCT[C/T]TCCACCACATACCTG	78514
rs238873748	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77418414	ACACAGGGCCTGTGA[C/T]ACAGGGTCTCAGGAC	78514
rs238874488	in-del	-/CCTTGCATTCACA			intron-variant	Arhgap10	Mm_Celera	8:77463825	GGACTAACGGGAGCG[-/CCTTGCATTCACA]CCTCACATCCATCCC	78514
rs238876571	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77479022	CATTCACTCCCAGCC[A/T]GCCACTGGCTCTGCT	78514
rs238884358	in-del	-/AAA			intron-variant	Arhgap10	Mm_Celera	8:77377854	ACACACACACAGAGG[-/AAA]AAAAAAAAAGAGAAA	78514
rs238885055	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77296166	GCCTGCCTGGATGCT[A/G]CCATGTTCCCACCTT	78514
rs238917726	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77412943	CGACCCAACACTAAA[G/T]TCTCTGTAAGTAAAA	78514
rs238924705	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77514189	GTGGCTTCTCCAAGA[C/G]AGCATTCCGATTTTT	78514
rs238935249	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77317384	AGATAAGCTGGGTAA[-/C]CAGTTTTCTAGTAGC	78514
rs238935525	in-del	-/TT			intron-variant	Arhgap10	Mm_Celera	8:77477142	TCCTGAAACTGTTTG[-/TT]TTTTTTTTTTAAGCC	78514
rs238959155	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77384172	GGAGCTTCTGAAGGA[C/G]TTCTCAGTCCTCACT	78514
rs238977778	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77329397	ATCCCTATCTTTTCT[A/G]TACAGGGCTAGGTTC	78514
rs238982027	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77340320	TTTGTCCTATAGACA[G/T]GCACAACAATGCCCA	78514
rs238988043	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77504904	TGGGCCTTTGACATC[G/T]AAAGCCCATCCCCAG	78514
rs239004416	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77332081	GAGGATGATGACAGC[A/G]TCCGAGATGAAGGAA	78514
rs239006110	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77287665	TGCCATGCTCAAGCC[G/T]GGCGTGGTGGTGCAC	78514
rs239011575	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77439234	ACTGAGGTCAACGGT[G/T]TGTAGGTCTGGAATC	78514
rs239015556	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77368614	TGCTGGCACTTAGAC[A/G]GTGCTTCGTGGCTGC	78514
rs239030546	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77411698	CCCCAGATGCTACAA[C/T]GGAAAGAGAGAAGCA	78514
rs239032827	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77454936	ACTTTATTGAGAATA[A/G]TGATTCTTTATAGCA	78514
rs239046346	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77374212	CCCCTGTATAAATCA[C/T]GTCGGAAATCCTAAC	78514
rs239049469	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77415931	CTCAAAAAAAAAAAA[A/C]ATATGACAGATGCTG	78514
rs239053416	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77453120	ATTTTTAAATAAATT[C/T]TTCTCGTTAATTGAA	78514
rs239059335	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77313227	CCACTTTCAGTACAG[C/T]ACTAGGCTCACAGGA	78514
rs239061967	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77366993	TTTACCTACACATAC[A/G]AGCATACAACTTGTG	78514
rs239063926	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77405067	AGCATTCAACGCTGG[C/T]TAATACGGCACAAGT	78514
rs239070955	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77417563	ATTTCAGTGTGGTTG[A/G]TATTAAAAAATAAAA	78514
rs239071508	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77446168	CCTGCCTCCTGCAGC[C/T]TCTGGCCTTGCTGCC	78514
rs239082404	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77268015	GGCAGGTGGCTGCCT[C/G]CAAAGCCCAGGAGAG	78514
rs239085257	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77402690	AAACCTTATTATGAC[-/A]AAAAAAAAAAAGAAA	78514
rs239092296	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77330674	GGATGGCTGCAAAGA[-/G]GGAAACGCCAGGTAA	78514
rs239093082	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77481812	GAAGTCTCTATGTGA[A/T]TTTCCCAGAATTTCT	78514
rs239093355	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77422054	CATGGCCTACATATG[C/T]CCTGTAAAGCCTGGC	78514
rs239110407	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77460485	AGAAAATGTGGAGAT[A/G]CCAGTCACACAGTGA	78514
rs239111479	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77485947	CAGAAAACACAGACA[G/T]TTTCATTGGGATTCA	78514
rs239118792	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77273454	AAACCCAGCATATTC[C/T]CATTAATAGAAGTAT	78514
rs239121681	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77313916	GCTGGCAGCACCGCC[A/C]GTTCCCAGAACTAAG	78514
rs239122155	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77466656	TGCTCCTCCAACACC[A/G]CACCACTAACCTGCT	78514
rs239130258	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77387126	aagaaaggaaggaag[A/G]aagaaagaTTGATTC	78514
rs239131872	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503779	TCAGGCAGGAGCTAC[C/T]CATTACTCCATCGCC	78514
rs239136330	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77360766	CTCTCATTAAATCAA[C/T]CATTTAAAATCTCAC	78514
rs239150017	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77294357	CTAGTGATATCACAG[A/C]ATACTTCCCTACTGT	78514
rs239154226	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77364921	TCCTGCTTATTAAGT[A/C]CCAGGAACGTGGATA	78514
rs239155659	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77509981	GAATAATTCTTAATA[C/T]ATAATATGAGTAAAT	78514
rs239166632	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77316456	AGTAACGCCCAGCTG[A/T]CTGCAGTTTCTGCTT	78514
rs239177031	snp	A/C/T			intron-variant	Arhgap10	GRCm38.p3	8:77355006	GCCTCTCTCACAGCC[A/C/T]GGGTCAGCAGGAGAC	78514
rs239192803	snp	C/T			utr-variant-5-prime, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77517859	GCTAGCAGGGCTGAG[C/T]GCGCGGCGAGCGCAG	78514
rs239195399	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77462812	GGCCTGGCTTTTTTT[C/T]TCTCTCCTCATAGAT	78514
rs239197140	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77297991	GGAAGTACATCACCA[C/T]AGGGGTGAGCTTTGA	78514
rs239206545	in-del	-/GAGA			intron-variant	Arhgap10	Mm_Celera	8:77334424	GAGTGGAGCAGCGCG[-/GAGA]GAGAGAGAGAGAAGG	78514
rs239216796	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77427952	TTAGGAAGCAACCAA[C/T]AAAGAATGGAGTCTG	78514
rs239218944	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77260719	ATGAACACCACTGAT[A/G]GAAAGCAGCTTGGGG	78514
rs239235874	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77287491	GGCAGGAACGCATTT[C/T]CATGTCTTGACATAA	78514
rs239235876	in-del	-/ACCCGGTCAT			intron-variant	Arhgap10	Mm_Celera	8:77369247	GGTGTGCGCCACCAC[-/ACCCGGTCAT]ACTAGACAATTATGT	78514
rs239239347	snp	A/C/T			intron-variant	Arhgap10	Mm_Celera	8:77355747	GAGGTTCAAACACAA[A/C/T]GTGCGCATGTGAATA	78514
rs239239454	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77347615	AGTCATAGGCTCCAC[A/C]AAAATGAAGACTGTC	78514
rs239239461	in-del	-/GT			intron-variant	Arhgap10	Mm_Celera	8:77443964	AGCAGAACTCAGAAA[-/GT]GTGTGTGTGTGTGTG	78514
rs239259884	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77462141	CAGAACTGGCAGGCT[C/T]CTAAGCATTCAACCT	78514
rs239270525	in-del	-/CAAAAAAACAAAAC			intron-variant	Arhgap10	Mm_Celera	8:77380681	CAGAGCACAAAAAAA[-/CAAAAAAACAAAAC]AAAAAAAAAACCTCA	78514
rs239276730	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77338913	ACAACCCATCATTGG[A/G]GGAAGCCAAGGAAGG	78514
rs239286208	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77500761	TGAAGCAGCAAGCAC[C/G]CTTACTCACGGAGCC	78514
rs239289057	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77285686	TGCTGACTGTGGAAG[C/T]AAGTGACAGTTTAAG	78514
rs239291728	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77274429	CCCAGGCATCCCCCC[A/C]ACCCTAGCACCTCAA	78514
rs239304763	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77348637	AAACAGGAGACACTG[C/T]ATGTTCAACCCCTGT	78514
rs239312054	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484850	ATTACAGGGAGCTCT[A/G]TCTACAACACAGGGT	78514
rs239324178	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77467971	GTGACACAGACACAT[A/G]GTAGCCATTTTCATA	78514
rs239328483	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77379165	CAGCCTCCTCTAACT[C/T]TGCAGCTGCTCTACT	78514
rs239356061	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77266547	TTCCGTCTTTAGGGT[A/G]TTAGCGGTCTGTGTA	78514
rs239357115	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77328308	GGTTTGTCCTTCCAG[C/T]TGTTTCCCTGACAAC	78514
rs239360744	in-del	-/TCA			intron-variant	Arhgap10	GRCm38.p3	8:77491838	GACTCAGACATGCCC[-/TCA]CCCCCGGCCCCCGAC	78514
rs239381120	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77270014	AAGCAAACTAAAGTA[C/T]GAATAAGGAAAGAGT	78514
rs239387747	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77308197	GAAAATGAGGAAATT[A/C]AAAAAATAATCAGAT	78514
rs239393811	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77469626	GAGTTCAATTCCCAG[C/T]GCCTACTCTGCAGCT	78514
rs239406098	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77409720	TTCTGCGCTCGTTTG[C/T]AAGGAGCCAGAATCT	78514
rs239406324	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77404892	CTGCCTCTGCCTCCT[A/G]AGTGCTGGGATTAAA	78514
rs239416274	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77456968	TATGTACTCACTGAT[A/G]AGTGGATATTAGCCC	78514
rs239419348	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77270527	CAACAGGGCAAATGT[A/G]CAGGTGAGCTCCCCT	78514
rs239437302	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77423769	TGTGGATCTGAGTTA[A/G]GACATAGTAGGCAGG	78514
rs239452679	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77475123	TGAATAAAGATACTG[A/G]TGGCCAATAGTTGAG	78514
rs239454809	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77468857	TTTTACAGGGGTTGC[A/G]TATCAGACATCCTGC	78514
rs239470951	in-del	-/CG			intron-variant	Arhgap10	Mm_Celera	8:77370719	GGCATGGTAATGACC[-/CG]CGCAGCCCTCCCATA	78514
rs239479075	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77323286	GCCTCAGGGGTAGCT[C/T]TACCTCCTCCCAATT	78514
rs239481815	in-del	-/CACA			intron-variant	Arhgap10	GRCm38.p3	8:77253730	TGAGATAGCCAGCAT[-/CACA]CACACTGCATGTGCT	78514
rs239490275	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77423510	GCTGCCCAGCCAGCC[A/G]TGGCAAATCATATCG	78514
rs239504687	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77457822	CAGTGCTGAGTACAA[A/G]CAGCACCTGACCACT	78514
rs239506507	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77397246	TTCTGGATTTAACTG[C/G]CCCTCAAGGTTGGTG	78514
rs239506647	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77510123	GCCTGGTGTACACCC[A/C]GGTCAGAAGAGGGTA	78514
rs239519629	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77380650	TATGAATTAAAAAGC[A/G]GTAATTAGTGATCCA	78514
rs239521932	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77326621	TTCCTGTGCTCCAGG[C/T]TGTCCTCAGGCATGA	78514
rs239549917	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77444544	ACACAACACTGACAG[C/T]GCTGAGCGCATCCGC	78514
rs239562057	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77271615	CATCATGGGACACAG[C/T]CATCTGGAGTAGAGC	78514
rs239578473	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77380996	GTGAGCAGCTGTGGA[C/G]AGCTGATGGCCTCTA	78514
rs239614975	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77450257	CACACTTAATGGAGA[A/G]GTGGCTCTCCTTAGA	78514
rs239615910	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494694	ATTTTAGCAAACAGA[A/G]CCACAAAGAAAAAAG	78514
rs239628464	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77421875	GAGCACCTTGCATCT[A/G]AACGTTCTGAGCAGC	78514
rs239631425	in-del	-/GGG			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519510	TAGTGTGGAACTGTT[-/GGG]GGGTGGGGGGGAGGG	78514
rs239637220	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77333570	ACGAGTGGCTTCCCT[A/G]TCCCTCCTGTCAGGT	78514
rs239642391	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77375032	CCGGTATCTTTCCTA[G/T]AGCATGACTGAAGCA	78514
rs239649360	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77273866	GATTATGAACGGAAA[A/G]CCTTGCTGTGGTGTG	78514
rs239658672	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77396172	TGAAAGAAGTCCACC[A/G]CGGAGGGCTACACGG	78514
rs239664061	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77464809	ACTGCTCTTCCAGAG[A/G]TCTTGAGTTCAGTTC	78514
rs239687389	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77449929	TTCAATATCACCAGC[A/G]CTATTGGATCTGAGC	78514
rs239691078	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77508169	TTGATAGAATGAGAT[G/T]ATAAGTGGCTGCTAG	78514
rs239691662	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77362699	CAGATGTGTACACAC[A/G]TTTGCTGGAGCTCTA	78514
rs239691840	in-del	-/GAA			intron-variant	Arhgap10	Mm_Celera	8:77480060	GTATCCTGGTTCAGC[-/GAA]GAAGAAGGAACCAGA	78514
rs239699344	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77355909	TTGGACAGTTTCGTT[A/C]GTGCACTAGGTATAA	78514
rs239701018	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77327844	GTTTTCATGATCTTT[C/T]GTTTTCTTTATATCT	78514
rs239701111	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77334001	CATAAAAGAAAGAGA[C/T]TATTCAAGAGCTGGG	78514
rs239701644	in-del	-/CG			intron-variant	Arhgap10	Mm_Celera	8:77378869	GAGTGAGCTACCCCC[-/CG]CCCCCATGGGCTTAC	78514
rs239731077	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77255398	ATATCTGCAGCATAC[A/C]GTGAGGAGCATGTCT	78514
rs239740524	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77415752	ATCAGAAGGACACTA[A/C]ACACTGAATTTGGTC	78514
rs239743666	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77443237	ATTTGTTATTACACA[C/T]GTGACTTGTGAACAG	78514
rs239749316	in-del	-/AGGG			intron-variant	Arhgap10	GRCm38.p3	8:77509567	TAAAGATTAAAAAAA[-/AGGG]GGGGGGGGATAAAGA	78514
rs239749725	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77401087	GTTATCATTCACAGT[G/T]CCTGCCAACTCTCTA	78514
rs239756673	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77356422	GAAAGTATGCTGATA[G/T]CATCAAGTATCCTGG	78514
rs239771322	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77274959	AAGATGGCCTAGTCA[A/G]CCATCAGTGGAAAGA	78514
rs239782215	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77288474	CACACACACACACAC[A/T]CTGCTTTCTTCCAAG	78514
rs239782997	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77414257	ACACCATGCGAGCTG[-/A]AGAGACAGAGCAGCC	78514
rs239786855	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77456054	ACCTAGAAGCTTGCA[C/T]TCCATGGCATAAAGG	78514
rs239794851	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77306553	GACCAGAAAAGAAAT[A/T]CCTCCTGTCACATAA	78514
rs239806521	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77448294	TGGCACTAACTGTGA[C/T]CTAATGTCATATTTA	78514
rs239807270	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77371675	CGGGTCACGCTCACC[C/T]CACACCTCCCAGGTC	78514
rs239811502	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77251443	TCACTGGGTAACTCT[G/T]CTGCTTCAGTCAGGA	78514
rs239812852	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77401651	AAAAGAAACTTAAAT[C/T]TTTATACGACTCACT	78514
rs239817622	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77255956	GAGACATCTCCTTTG[C/T]TAGAGTTATATGTAG	78514
rs239838223	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77376552	TGGCTGCAGAATTTC[A/G]GGGATGCATTTGCAG	78514
rs239869465	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77332536	TAAGATACTCATCTG[G/T]GAGGGCAACTGCACC	78514
rs239880951	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77436200	ATGGTGTTTCCATTA[C/T]GACTGTGGTGTGACA	78514
rs239883071	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77365521	TATACAGAAGAAAGT[G/T]TTTAGATGATTTCTG	78514
rs239884040	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77292811	CACAGAGGCATAGTC[A/G]AGACTACACAGGAAG	78514
rs239885899	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77308424	TAGAATTCTATCAGA[C/T]CTTCAAAGAAGACCT	78514
rs239910490	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77497145	TTATATTTATTTAAT[A/G]TATGTGTTTTGCTGG	78514
rs239910840	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77474601	TGAAGCGAGATTTTA[A/C]AACCACAGAAAACCA	78514
rs239914802	snp	A/C/T			intron-variant	Arhgap10	GRCm38.p3	8:77252384	TGACCCAGCAGGCAA[A/C/T]TGGATTTCTTCATCC	78514
rs239914886	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77320900	ACTTCAGTCTTCCAG[A/C]CCACCACTGTGACAG	78514
rs239919181	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77477545	GGAAATCTAAAAGGG[C/T]CGAGTTCCGTCATCT	78514
rs239928701	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77266653	TAAAAGTTTAATCTT[-/A]TGAAAGACACATACA	78514
rs239934654	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77405408	GGGGAGATGCACACA[A/G]AAATGTGGTGCCCAC	78514
rs239935434	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77329628	TTTGTTGTTTTCCCC[G/T]TAATGTGTTTTTGTT	78514
rs239948925	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77447575	TGAAACAGCCCTCAA[C/T]ACAGAACCTCTCTGC	78514
rs239952123	snp	C/G			upstream-variant-2KB, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77518038	CCTGCTCTCCCGCCC[C/G]GGCGCCTTCGGCTCT	78514
rs239957199	snp	G/T			intron-variant, downstream-variant-500B	Arhgap10	Mm_Celera	8:77358481	CTTTGGAGACTTCTC[G/T]TATCAGTAAGTGTCA	78514
rs239958566	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77442978	TTGTAAAATAAGTAA[C/T]GGGCAACTTTTGCTT	78514
rs239960818	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77265668	CAGGGCTGGGGTTAG[C/G]GTGGCCATGACTGGT	78514
rs239979033	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77276859	AGCCCATAGGAGTGC[A/G]AGCACCCCCATCCTG	78514
rs239980844	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77271350	AATTCCTGTCCTGAC[A/T]TCCTTTGGTGATGAA	78514
rs239992257	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77488842	GGGTAGCAGAGCAGT[A/G]GTATGGACCAAACAA	78514
rs239993266	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77483700	CCCTGCCCCTCCCTA[C/T]AGGCTCCAGCTGTGA	78514
rs239997881	in-del	-/AACAACAAC			intron-variant	Arhgap10	GRCm38.p3	8:77414034	CACTCTTTCCAAGCT[-/AACAACAAC]AACAACAACAACAAC	78514
rs240012461	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77463799	TTTAAAGAGTTTTCA[A/G]AAAGTCAACAGGACT	78514
rs240017123	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77370515	CAGCCTGCTGAGGCA[A/G]GGAACAATGAGAAGG	78514
rs240021013	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77352272	GAACTGTATTAAGGG[A/G]CTGTAGCATTAGGAA	78514
rs240021841	in-del	-/AG			intron-variant	Arhgap10	Mm_Celera	8:77400611	TAGTGCTGGAACTAT[-/AG]ATGGTTATGACATGG	78514
rs240030369	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77377852	CACACACACACAGAG[-/A]GAAAAAAAAAAAAGA	78514
rs240030558	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77404411	AGCAAAATCATATAC[-/A]AAAATATTAGTTAGC	78514
rs240030838	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77344252	ACCAGCAGGTCCCCG[A/G]TCCGTGTTACTTCCA	78514
rs240035291	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77362223	CAGCAAAGGGGAAAA[C/T]ATCACAGGAAGGAAG	78514
rs240037856	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77449230	CCCTGGCCCTGTGCA[C/T]ACTGCCACATCCCTG	78514
rs240039059	in-del	-/ACC			intron-variant	Arhgap10	GRCm38.p3	8:77404550	CATCCGAAAGAAATA[-/ACC]CAACTCCAGAGAAGC	78514
rs240040915	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77298580	CAGCTGTTTAGAGCA[C/T]TGACTGCTCTTTCGA	78514
rs240042113	snp	A/C			intron-variant, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77517298	GGAGACTGGAAGCAG[A/C]GTTAGGGCGCAGTAA	78514
rs240045694	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77291345	CAGAGATACCCCACC[A/T]TCACTCCAGGGCTCT	78514
rs240054076	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77434723	ACCTTAACCAAACCC[A/G]CAGTTCAGTAAACTA	78514
rs240058211	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77342281	AGAAAGAGAGCTGGG[-/A]AAGTGATGTAACTGT	78514
rs240058552	snp	A/G			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519451	GGCTTGAATAAGAAT[A/G]ATTCCCACACAGGAT	78514
rs240071101	in-del	-/GGGGC			intron-variant	Arhgap10	Mm_Celera	8:77370111	ATCCTGAGGGGGGGG[-/GGGGC]GGGGGAATAGGAAAG	78514
rs240080560	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77429792	AGGGCGTGCTTACTG[C/T]TCTCCCACGGAGCCG	78514
rs240087805	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77339791	CCCAACGGGAAGGAA[C/G]CTTACTCCTGCAGGA	78514
rs240093773	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77406207	ACCCACCCCTAAAAG[A/G]AGGAAAAAGTATAAA	78514
rs240099966	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77253074	GCTGCTGCTGCTGCT[A/G]TAATCAATGTGGGAA	78514
rs240110114	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77421838	CTCACGTGTCCTCGG[A/T]ATGACTTGCCCTCAC	78514
rs240134405	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77291500	TATACACACTCCTAG[A/C]TTTCTATGATTATTG	78514
rs240136421	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77331361	GGCTAAGTCATGTCC[A/G]CTCTCTAAGCCTTAG	78514
rs240142034	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77471297	TTGTGAGACTATGCC[A/G]GGGCCTAGCAAACAC	78514
rs240146403	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77284160	GTCAGTGACTGCTGA[A/G]GCCAGGAGCTAACAG	78514
rs240152620	snp	C/T			upstream-variant-2KB, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77518393	GCACGCCGGGTGCTC[C/T]CTCTCCTTGTCTAAT	78514
rs240157801	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77253114	TAGAACCCCTGCCTC[C/T]CCTCCTCTGAGTGTA	78514
rs240164894	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77274912	TAACCAGTACCTCCC[A/G]GAGCTCGTGTCTCTA	78514
rs240171570	in-del	-/CCAAGG			intron-variant	Arhgap10	Mm_Celera	8:77258890	AGGGCATCTATAAAA[-/CCAAGG]CCAACAATACCCAGG	78514
rs240178195	snp	G/T			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77515632	GAAAAGATAGCGCTG[G/T]CTGGCTGCTCCCTTA	78514
rs240178662	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77308780	ACATTTTCAAATAAA[-/T]TTTTATTAGTCAGAA	78514
rs240197827	in-del	-/AAAGG			intron-variant	Arhgap10	GRCm38.p3	8:77365661	TTGAACACAAAAGAC[-/AAAGG]AAAGAGAAGTTACTC	78514
rs240198479	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77470500	CAGGAGGTTACTAGA[C/G]AAATTGAATGTTATG	78514
rs240198706	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77325506	CTGCTAAGGCAGCCT[C/T]ATACGACAGAAAACT	78514
rs240200381	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77476323	ACATTCCAAATCTAA[G/T]ATAATGGATCCTTCT	78514
rs240213167	snp	A/C/T			intron-variant	Arhgap10	Mm_Celera	8:77382040	ACATAAGCTCAAGCG[A/C/T]GCGCGCGCACGCACA	78514
rs240215842	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77334766	GCTTCCAGACTAGGC[C/T]TAGGTCTGCAGAGAC	78514
rs240252987	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77270431	CCTCACAAGGCTCAG[G/T]AACCATCATGAGGAG	78514
rs240254123	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77399057	CTCTCCAGCCATGAA[A/C]ACCTCGGATAAAGGC	78514
rs240257014	in-del	-/TA			intron-variant	Arhgap10	Mm_Celera	8:77275158	AGAAGCATTTATCTG[-/TA]TAGCAAAGATAATCT	78514
rs240257685	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77445429	GAAGGTCTGCGCTTA[C/G]CTTCTGGGAACCTGC	78514
rs240259274	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77264602	GGCAACCAACGTTGC[C/T]ATGAGTAGGTTGGAC	78514
rs240261536	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77455640	AAACACCTCTGTAAG[A/G]TAGTACTTCAGGCGA	78514
rs240262345	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77475852	TGAGGACAATAAGCT[C/T]ATACATAACAATTGG	78514
rs240263246	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77316140	CTATCACAGGAAACC[A/G]GAGAGGGACTTTAGG	78514
rs240270977	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77407452	GATAGATAATTAGAT[A/C]AGACAGACAGACAGA	78514
rs240272538	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77459473	AAGAGGTCAGGGATC[C/T]GGGGCAAGGGCCAGG	78514
rs240278118	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77375998	ACCAAGAGAACTCGA[C/T]CAAGTTCTCAAGTTT	78514
rs240293868	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77350326	CTCTAAGACAAACAG[C/T]CTGAAACTGTCTTCC	78514
rs240294868	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77441433	CAAACCCCACCACCA[A/G]AATAAGACCATCTTT	78514
rs240327414	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77316712	GGAGCCCCTTTAGCC[C/T]AAAGCAAAGACCATG	78514
rs240341374	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77376671	TTAAAACAGAGATGG[C/G]GAATGAGAAAGCTGT	78514
rs240347299	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77275857	CGCATGATGTCACTG[C/T]CCTGCAGAACCACGA	78514
rs240347990	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77252148	CTGCAACCATGCCTG[A/G]GCAGCACAGACTCAC	78514
rs240362306	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77424342	GGTGGTGGCATGACC[A/G]CTGCAGGGCTTCCTG	78514
rs240389309	in-del	-/GAAGGG			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493315	GGAAGAGGAGGAGGA[-/GAAGGG]GGAAAGGAAAAGAAA	78514
rs240398169	in-del	-/GGT			intron-variant	Arhgap10	Mm_Celera	8:77486050	GGAACTGTATTAAAG[-/GGT]AGTAGCATCAGGAAG	78514
rs240424738	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77430433	CCAGAAAAAAGAAAC[A/G]GCGTGAAAATGAGGT	78514
rs240436425	in-del	-/GCA			intron-variant	Arhgap10	Mm_Celera	8:77359457	GGCTGTTAGTGGCTT[-/GCA]CCTTTAATCCCAGCA	78514
rs240443534	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77288558	CTAGAATCAGGCTGT[C/T]AGAGCATCATGGGTC	78514
rs240444164	snp	A/C/G			intron-variant	Arhgap10	Mm_Celera	8:77310175	GCTGGCAGGGATAGC[A/C/G]TGGTTGGACGGGAAA	78514
rs240466630	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77381409	TTGCCTGCAGCCCCA[C/T]CTTATGGAGGCATTT	78514
rs240473456	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77421051	CACACACACACACAC[A/G]CGCACGCATCCACAC	78514
rs240474127	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77422988	GAGTAGAGAGAGCAA[A/G]ACAGAAATGAAACTG	78514
rs240475174	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77252822	GTTTCTTGGTGACCT[C/T]GAGCTTCCTATCTAA	78514
rs240491186	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77388478	AATGGCCCCAGTGTG[C/G]GTGTGCTGCAGCTGA	78514
rs240498833	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77278149	CATGCCCGTGAACAC[C/T]GAAGGGATGGTGCTG	78514
rs240507914	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77446847	GTCAATCAAAACAGC[A/T]GCAGAATTAGGAATA	78514
rs240509920	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77381434	CATTTCCAGACTGAG[-/C]GCCCCCTCCTCTGAG	78514
rs240512044	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77324235	CACCCTTCATCCAAC[A/C]CTGTACACACAGAAG	78514
rs240520458	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77352302	AGGTTGAGAATCACT[A/G]ATAAAGAGGAAACAT	78514
rs240523664	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77487351	CATGCACGCACGCAC[A/G]CACAGATACACACTA	78514
rs240532577	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77317875	AAATAATGGTGAAGC[-/T]TTACCGCCATTAGGC	78514
rs240548569	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77470833	CCACGTGCATTCAGG[C/T]GCCCACAGGGCCCAG	78514
rs240551240	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77411475	ACACGTGCACACACA[C/T]GTGCACACACATGCA	78514
rs240552893	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77409140	GACCTCACTGGAAGG[G/T]TTTGCCTATGATCGC	78514
rs240566919	in-del	-/CAAAA			intron-variant	Arhgap10	Mm_Celera	8:77359583	GAGAAACCCTGACTC[-/CAAAA]CAAAACAAAACAAAA	78514
rs240567459	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77330903	ATGCAACCATTTTTT[G/T]AAGATTTGGTCTGGC	78514
rs240574163	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77269007	TGACAGCTGGGTCTT[A/C]ATAATCTTGGTGGTA	78514
rs240579931	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77413476	CTCTTCAGATCGAAG[C/G]CATCCAACACCCTCC	78514
rs240596499	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77472079	CCACAGCTGGTGTTA[A/T]GATTTCACACCCCAA	78514
rs240603527	in-del	-/AGAG			intron-variant	Arhgap10	Mm_Celera	8:77489213	TATATATACACACAC[-/AGAG]AGACATTCACATACA	78514
rs240614818	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77406967	TGGAAACAACAATAA[C/T]ACAAAACACGTACAT	78514
rs240617170	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77411849	GCTCCTCAGGCACTA[C/T]GGATTAAACAGTGGG	78514
rs240619195	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77463734	GCCTATTAGAATGCC[A/G]ACAAGCAATACCAGG	78514
rs240621527	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77404667	AAAATAGCAAAAGCA[A/G]ATACTTGGAAAGAAG	78514
rs240643063	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77426573	AGCTTCTGAGACAGC[A/G]CCACTCTCTGACTCA	78514
rs240644807	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77356866	TAAGTTGATTAAATA[C/T]GACTTGATCTGACCC	78514
rs240667598	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77395837	AGAGTCAAAAGTACT[A/G]AGAACAGCAAATGTT	78514
rs240673730	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77253562	ATGACAAATGGCCTT[A/G]GCACAAGAGAACACA	78514
rs240687982	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77469849	TTCCACCAGGCGTAT[A/G]CTCTTAAGTGCCCTT	78514
rs240695014	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77312570	TTGTGCCTCTTCCTC[C/T]ACTGCATTTGAAGAT	78514
rs240704078	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77426124	AACACTGACTAACAT[A/C]GCTCCTGTGAAAACC	78514
rs240704250	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77433325	TGCTGGCAGGCAACG[A/C]ATGGGGTGCAGGGGG	78514
rs240708108	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77513763	GGTAACAATGGTTAG[A/G]ACTGCTGCTGACACC	78514
rs240711315	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77462748	TATGTTACATATGGA[A/G]TCTGGGCAGAATATA	78514
rs240722747	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77357218	TGTGTATTAGTATAG[G/T]AATATATCTGCAAAA	78514
rs240732708	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77382719	CGGGCAGAGCATGAC[C/T]GTTACCTCGGGTTTC	78514
rs240733276	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77297063	AAGTGCTTTTCAGGC[A/G]CCTTATATACAGGTT	78514
rs240746861	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77505641	CTCAAGAATAACAAC[A/G]AAACCTTTTAACATA	78514
rs240749908	in-del	-/AAG			intron-variant	Arhgap10	Mm_Celera	8:77450166	CACAAACTTACAAGA[-/AAG]AAGAAGATCTCTGAA	78514
rs240753129	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77447242	ACTGAGATTAAAGGC[A/G]TGCAGGACTCTGCAG	78514
rs240770512	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77498396	GTGGTTTAGACTGAA[C/T]GCTGCCCACCCACCC	78514
rs240770692	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77285530	CAACATTTTATCAAG[A/G]GAAGCAACAGAGCAT	78514
rs240788432	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77383318	ATTATTATTTTCATA[A/C]TTTGAACTGAAACAG	78514
rs240806879	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77499565	TTTACACCATGACAC[A/G]AAACAGCATCCACAG	78514
rs240809600	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77447042	AGGTTTTTTGTTTTG[G/T]TTTGGTTTGGTTTAA	78514
rs240812727	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77452587	CCTGTATCCCCAGAC[A/G]TGGTGGCACGTGCCT	78514
rs240829570	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77336081	TTGTACTTTAGATTA[G/T]ATTAGGTTAGTTAGA	78514
rs240830559	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77497953	GAGACATAGCCTCTG[C/G]GCCAGACTGTGAGGG	78514
rs240832151	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503871	AAATGGAGGGCCTCA[C/T]AGCAGTGCGGGGAGC	78514
rs240837038	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77408428	AAAGACTTGTCCTTC[C/T]GGGCAGAATGTACAA	78514
rs240838284	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77440289	GCCTCTCTAGGTGCA[C/T]GGGCCACCCTTGACT	78514
rs240858553	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77277024	ACAAAGATTTTGCCT[G/T]GCCACCTCCCTTGGG	78514
rs240873226	in-del	-/GGT			intron-variant	Arhgap10	Mm_Celera	8:77282167	TAGTTAGTAGAATTC[-/GGT]GGTGGTGGTGGTGGT	78514
rs240873285	in-del	-/CAGGTATC			intron-variant	Arhgap10	Mm_Celera	8:77459599	CTGGCCTTGAACTCA[-/CAGGTATC]CTCCTACCTCAGTCT	78514
rs240873651	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77468118	TTCCTCCTGCACTGA[-/C]CACCCCTCCTCCTTG	78514
rs240877316	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77481011	GACACGTGAAATGAC[A/G]GCCCACTACCCGCAC	78514
rs240877662	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77453763	ATGAGGTATCTAAAT[C/G]GGCCCTGACTGTCCA	78514
rs240877941	in-del	-/CCCACA			intron-variant	Arhgap10	GRCm38.p3	8:77252681	CCAGCGTTGTCAGGG[-/CCCACA]CTGCAGCTGCTCGGG	78514
rs240878466	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77452318	CCTCACTTTTTTTTT[G/T]TTGTTTTTGTTTTTT	78514
rs240886577	in-del	-/TG			intron-variant	Arhgap10	Mm_Celera	8:77401389	CGACCCATGGAGCAC[-/TG]TCTTTCCACACACAT	78514
rs240895030	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77330479	TACTTGTGCTTATTA[G/T]CACATTAAGCACATA	78514
rs240895638	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77365734	CTTCATGTGGACTCT[C/T]ATAGCTAAGTGACAC	78514
rs240901216	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77403617	GTATACTTGATTCAC[C/T]GTAAGTGAATATATT	78514
rs240907313	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77358793	CTGCAGAAAGCCTTC[A/G]GGAAAGACAAAAGGA	78514
rs240922377	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77355771	GTGAATACGAAGCCC[C/T]GATTTTACCAAGTTA	78514
rs240925738	in-del	-/CATTTCCACGGT			intron-variant	Arhgap10	Mm_Celera	8:77316855	AGAAGCCCAGCACTG[-/CATTTCCACGGT]CATTTGAAAGTGCTT	78514
rs240925959	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77446914	AGTACGTGTAATTTA[A/G]CACCGTATTCTTGTT	78514
rs240926495	in-del	-/CCC			intron-variant	Arhgap10	Mm_Celera	8:77387883	CATCTTCAGATCATG[-/CCC]CCCCCCCCAAGTCTT	78514
rs240927007	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77424244	AACAGCTGCCCTTGC[A/C]GAACAGACTGGGGGG	78514
rs240935217	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77453074	TAAGGACAGTATGTT[A/G]TATGGACAGAAATAA	78514
rs240935331	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77258233	TGTGAGTTCCTGTCC[C/T]GACTTCCTTTGGTGA	78514
rs240943343	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77311378	TACATTCTTCATAAT[C/T]TCCTTATTTAATGCT	78514
rs240950730	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77467457	CAGGTCTATAGGACA[C/G]CCAGGGCTACAGAGA	78514
rs240952330	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77408801	ACTAGTCTTCAGGGA[A/T]TTTACTCATGGGCCT	78514
rs240960690	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77482177	TCTATGTGCCACATC[-/A]AAAAAGGCCACCAGA	78514
rs240964896	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77359410	TTCCCTTTAGAAGAA[G/T]GGCTAGTGTTGTAAA	78514
rs240966384	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77487399	CTTTAAAAAACTTCT[C/T]TTTGTGTGTGCATGT	78514
rs240984736	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493883	ATACGAGTACTCCAC[A/G]CCACAGCTCAGAGAG	78514
rs240993129	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77311718	CCTGAAATAAAACAC[C/T]GGAGCCATGGGCCTG	78514
rs241013869	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77253284	TGCTCCCTTCTCCAG[C/T]GCTGGAATGGTGTGA	78514
rs241013968	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77258863	CTTTCAAATATACCG[A/G]AGGAGGAGTGTAGGG	78514
rs241026575	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77457707	CCTTTGGCAGTCCCA[C/T]TAGAAAGTCTACACT	78514
rs241032467	in-del	-/TC			intron-variant	Arhgap10	Mm_Celera	8:77453229	TTGAGGGTTTTTTTT[-/TC]CTTTTAACATGTAAG	78514
rs241047985	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77334602	GCCAGATTGAATCAA[C/T]AAGCCTGGAGACGAG	78514
rs241050050	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77337673	CCTCCGAGGTCAGCA[A/G]TCTTTACCTCAGCCC	78514
rs241051551	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77369566	TATCGTTCATTTTCC[C/T]GGACATGAATGCTCA	78514
rs241055615	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77445493	GAGGAGAGACAGAGG[C/T]GGGATTTTAGAATTT	78514
rs241062232	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77418816	AAAACACAGATATTT[A/G]CATTAGGACTCATAA	78514
rs241074394	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77312172	CACAGGAAAACTGAC[C/G]ACGTGCCTTGAAAAA	78514
rs241075228	snp	A/C/T			intron-variant	Arhgap10	Mm_Celera	8:77279543	ACCAGAAAGAGGAGG[A/C/T]GAGAGTTTCTATGGC	78514
rs241090085	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77403435	AACCTATTTCTCCAA[C/T]CAAAGATGAGTGGCA	78514
rs241091213	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77499686	AAAAACCCTTTCACA[A/G]GGGTCCCCTAAGGCC	78514
rs241094919	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77476991	ATGGACCAAATGTCT[A/C]TGTTCCCACAAAATG	78514
rs241099824	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77296349	GGTGGCTCACAACCA[C/T]CTGTAATGGAATCTG	78514
rs241113153	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77432116	ACCAGGAAGTGTGTG[-/T]GTGGGGGGGGGGGTG	78514
rs241115700	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77274298	TCCTTTTTAATTTAA[-/T]TTTTTCATTTTTTAC	78514
rs241119689	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77373614	ACACACAATATTATA[C/T]TTCTATCTACATATT	78514
rs241133317	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77423329	CCTGGCTGCCCCAGG[A/G]ACGAGGAGACCCTTA	78514
rs241134887	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77432428	TTAAGGCTGGCATAG[C/T]GTCACAGTTCCCTAT	78514
rs241137570	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77445165	ATTTACCTGCTAAAG[A/C]CCAAAGTCCCACAAA	78514
rs241144324	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77273007	GCATAAGAGATATGT[A/G]GTGATATCCAGACGG	78514
rs241152210	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77450614	ATGCATCAAAACTTC[C/T]ATCAGGCTCAGCTCC	78514
rs241152467	in-del	-/AAAAAA			intron-variant	Arhgap10	GRCm38.p3	8:77329916	AAGCAATACTACATT[-/AAAAAA]AAAAAAAAAAACCAT	78514
rs241168072	in-del	-/TG			intron-variant	Arhgap10	Mm_Celera	8:77401604	ATTTTGTTTTATTGT[-/TG]TTTTTTTTTAAATAA	78514
rs241174742	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485620	ACCTCCATTTCCACT[C/T]GGTCAACACCAGTTA	78514
rs241177462	in-del	-/GC			intron-variant	Arhgap10	Mm_Celera	8:77454125	TTGACACCTGGAGAA[-/GC]GCACGGGCTGGGACC	78514
rs241190710	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77365027	TATATCAAATATTAA[C/G]TTGCAAAGTCAATGA	78514
rs241197117	snp	A/G			intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77493036	TGGAAGGCAGAGGCA[A/G]GTGGATCTCTGTGAG	78514
rs241200656	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77482603	ACTTCACGTCACATA[A/G]AAAAAGTAAGTGGGA	78514
rs241204114	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77272994	ATCAGACTGAATAGC[A/G]TAAGAGATATGTGGT	78514
rs241215850	in-del	-/GT			intron-variant	Arhgap10	Mm_Celera	8:77428939	TGTTTTGGAAGAGAG[-/GT]TTTTTTTTTTTAATT	78514
rs241220021	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77273378	TGCAGGAGACACACG[A/C]AGGTCCTTGGGAGAC	78514
rs241223687	snp	C/G			intron-variant, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77517334	GACTCCGGAGCAGAG[C/G]CTCCATTCGCTCCGG	78514
rs241228196	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77440873	GATGATGAAAAGAGC[A/G]GTGTACACAAACACA	78514
rs241228454	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77433494	ACAGTGACTCACTTG[A/G]GGGTTTTCATTCAAA	78514
rs241228867	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77402490	TAAAAAATCTTTTTT[A/T]AAAAAGTCATTTCTC	78514
rs241231659	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77342918	ATGTAAATTTATGTG[C/T]GGCCAAACTGCTCCA	78514
rs241233937	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77316666	TGCCAGTTACGATGC[A/G]CACCAGTCACGTACT	78514
rs241239869	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77408549	GATCAAGGCAGATAA[A/C]GCTCACAAGGACAGA	78514
rs241243939	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77348507	CAATGGTAATGTAAG[A/G]AGGTTACGAAGGAGT	78514
rs241244034	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77269574	ACCAACATTTAAAAG[-/AA]AAAAAAATTATCTCC	78514
rs241252362	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77354265	TGTTTCCTGCACACA[G/T]CTTGGTCCCAGCATA	78514
rs241265147	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77295583	AATAAACTGAATATC[A/G]GGCCAAGAAGTGGGA	78514
rs241277659	in-del	-/GGGG			intron-variant	Arhgap10	Mm_Celera	8:77451323	AGAGAAAATGAGAGA[-/GGGG]GAGGGAGGGAAGGCG	78514
rs241278993	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77440378	ACAAGCTAAGCACCT[A/G]TCTTATACAAGAAGC	78514
rs241284312	snp	C/T			intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77492776	TATACCCTAGGAGTT[C/T]GAGCTGACACTGCTT	78514
rs241284527	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77309095	GACTTCTGCTTTCCT[C/T]GAAGGCCATTGGGTA	78514
rs241285288	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77343651	TTGCCCCAACCAAAG[G/T]TGCTTTTTGGTTAGA	78514
rs241285800	snp	A/C/G			intron-variant	Arhgap10	GRCm38.p3	8:77383991	TGTGCTGTGTGTAAA[A/C/G]AGCTCAGCACCTCAG	78514
rs241309901	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77289639	GTTACACGGCAACTT[-/A]CACATAGAGACACCC	78514
rs241322326	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77340908	GCATGCATGCACGCA[C/T]ATGCATGCGCGTACA	78514
rs241327246	in-del	-/CT			intron-variant	Arhgap10	Mm_Celera	8:77341903	GAAAAAAAATAAAAA[-/CT]TAAAAAATACGAACT	78514
rs241329899	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77449789	CAGACCATGTGGATC[A/C]GTTTCTCCATTCATA	78514
rs241337461	in-del	-/TGAT			intron-variant	Arhgap10	Mm_Celera	8:77414917	CACACACAAACACAC[-/TGAT]ACAAACACACACACA	78514
rs241343577	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77472687	TATGTTTATATATTT[A/G]CATGCAATATATACT	78514
rs241344622	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77337177	GGAAACACCCCACAA[G/T]CGGGGAAGCAGAGCC	78514
rs241351185	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77384403	TGAAGGCCTACGGCA[C/T]GCGTAGGACCATGAG	78514
rs241358320	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77491462	ACACTACCAGTACTG[C/G]ATCCTCACCAGGACT	78514
rs241375384	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77328736	TAACGGCCTCACAGG[C/T]GACATCTCCTTCCAT	78514
rs241376149	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77267300	AACCTCCCCCTTTAA[-/C]GAGAAAGGCCACAAC	78514
rs241405939	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77379086	TCCAAAGCCCCTGGG[A/G]CCCAGTGAATAGGTT	78514
rs241406698	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77409292	CTGATGTCAATCAGA[A/G]GTGTGGCAACAATGA	78514
rs241438171	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77291994	GGTCTATAAATCTTG[-/T]GTTTTTTTAAAAGAA	78514
rs241453014	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77379737	CTCCATTAGCACTGA[G/T]GCCTTCCAACCCATG	78514
rs241454124	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77279628	GAAAGGTTATGGAAC[A/C]TTTAAGAGGGGGAGC	78514
rs241455522	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77468711	ATCTGCCCAGCTGAG[-/C]CCTAAGGCTTTGAAA	78514
rs241458023	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77319468	ATTCTTGAATAGTCT[C/T]GGGTTGTTTCCTAAT	78514
rs241465368	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77323123	GAGCGAGAAAATGTG[G/T]AACTGTCACCAAGCT	78514
rs241484674	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77267527	TCCTTTCAGAAAATT[A/G]TAGGCCGTTAGAGAT	78514
rs241485903	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77407610	TGTGCTTACAGCCTA[-/G]CACAGCAGCACAGCC	78514
rs241490060	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77499072	AAGGCATCTGCCACC[A/G]CTACCTGGCCTTCCT	78514
rs241499192	in-del	-/AGTC			intron-variant	Arhgap10	Mm_Celera	8:77496300	CCAGAATGCCTGCAG[-/AGTC]AGTCACCTTGCCCTT	78514
rs241506712	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77260276	CCGAAAGGTATTTAC[A/G]TGTGGGAATTCAGAA	78514
rs241507117	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77361080	TTCGCAATCAGTGAG[C/T]GAAGTGGAATTTGTT	78514
rs241519172	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77272178	GGATACAGCGTTTCT[C/G]TATAGCGCTGCAGAG	78514
rs241522094	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77430373	CTCTAATGAACATCG[A/G]CTCTCAAGGTGCTGG	78514
rs241536936	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77312953	AATGGCACTAGACAC[A/G]CACCTCAACTCCTTA	78514
rs241545253	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77260859	CCAGTGGTAGCACAG[A/C]ACGCAGTAGGCTAGT	78514
rs241547684	snp	A/C/G			intron-variant	Arhgap10	Mm_Celera	8:77434360	CCCTCACAGTAGAAG[A/C/G]GAATTGACCCCCTCG	78514
rs241566003	in-del	-/AA			intron-variant	Arhgap10	GRCm38.p3	8:77451719	GAACTTTATTTTTTT[-/AA]TAAAAAATGGGCAAA	78514
rs241571246	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77313795	TATTGATAAGGGCAC[A/G]CTTTTCCAGGCCAGA	78514
rs241583822	snp	A/G			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519323	AGCTGAGGCAAGAGG[A/G]TAGAGAGTTTAAGGC	78514
rs241587645	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77438629	GCCCTGCCACCGAGA[C/T]CGTCAGAAAGCCGCT	78514
rs241592561	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77261811	GGACAGTAAGGCTCT[C/T]GCAGAGGATTTAAGG	78514
rs241606984	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77331208	TATCATTTAAACTTT[-/A]AAAAAAAAAAAGTTG	78514
rs241614937	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77449894	CAGACAGGCATGAGT[-/AA]AACCACGTTAGTAAC	78514
rs241617593	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77281429	AAAGAGCATGGACAC[G/T]AAACGAGCCTCCAAG	78514
rs241625132	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77254385	ATTCCCAGCAACCAC[A/C]TGGTGCCTCACAACC	78514
rs241629245	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77354830	CTTCCCTATGAACCC[A/G]TCCCGTCTTCCACAC	78514
rs241632504	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77296628	CAAATATTGGCAGGG[-/AA]AAAAAAAATCTACCT	78514
rs241642673	snp	C/T			downstream-variant-500B	Arhgap10	Mm_Celera	8:77249904	ATACCGAGCTTTCTT[C/T]CCCATAAGACTGGGC	78514
rs241653723	in-del	-/AAAAAAAAGAA			intron-variant	Arhgap10	Mm_Celera	8:77506618	CAGGCAGACACTACC[-/AAAAAAAAGAA]AGAAAAAAAAAAAAA	78514
rs241653975	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77407287	ACCATCTACAACTCC[A/G]GTTTCTGAGGATCCA	78514
rs241656391	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77473049	TTAGCTCAGGAGAAC[A/G]GTGACCAGCAGTAAA	78514
rs241670593	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77333510	TATTACTGCAATGAG[A/G]GATTTCCTGAGGCTG	78514
rs241678431	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77360981	AAGCAGCTGTCACTT[C/G]AGAAGTTAATGACTA	78514
rs241682767	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77286548	GTAGCTGGAAGCTCG[C/T]ACATTGAGAGGGAGG	78514
rs241686768	snp	C/T			upstream-variant-2KB, downstream-variant-500B	Arhgap10, 0610038B21Rik	Mm_Celera	8:77518918	GTGATTCTTTAAAAA[C/T]GTTCCGACTGAGTGC	78514
rs241687427	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77467209	CAAACAATTATGAAC[-/T]TTTTTCTCTCTCATC	78514
rs241691048	in-del	-/AAA			intron-variant	Arhgap10	Mm_Celera	8:77269573	ACCAACATTTAAAAG[-/AAA]AAAAAAAAATTATCT	78514
rs241732878	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77408918	GTTCTTAATCCTCTC[C/T]GTTGGAAGACTTACT	78514
rs241745312	in-del	-/A			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494074	TAAAGTCACTGTGAT[-/A]GGGGCTAAAATGCCT	78514
rs241763444	in-del	-/TG			intron-variant	Arhgap10	Mm_Celera	8:77368202	GGTGGAAGATGTAAC[-/TG]ATATGCCAAACTACA	78514
rs241766399	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77366755	ATATTGAGATGAATT[A/C]AACCTTCAAGCATGC	78514
rs241771775	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77480371	AATAGGAAGCAAAGT[C/G]TTGCCAGTAAACATG	78514
rs241779195	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77398230	CCAGAAAAGGGCATC[A/C]GATCTCATTCCGAAT	78514
rs241800688	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77436290	GAGATGGCCGTGGAC[A/G]TGTCTCCATGGCAGA	78514
rs241803997	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77428418	AGAGCAATATAAATA[A/C]ATAAATGGAAGAGAA	78514
rs241819381	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77443522	TTCCAAATCCTATCA[A/G]GGTGACAATGGAAAC	78514
rs241833351	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77385220	ACTCCTACAGGGCAC[G/T]GGAGCTCCTCGAGCA	78514
rs241833447	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77398670	AATGTTCTAAGACTA[C/T]AGACAAGGCTCTGAG	78514
rs241839836	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77373357	AGGAACCTTGGATTC[A/T]GAAAAATCTAAAAAC	78514
rs241848715	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77449849	AGACTGACATGCAAT[C/T]CAAAGACTTGAAGTA	78514
rs241861188	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77443966	CAGAACTCAGAAAgt[A/G]tgtgtgtgtgtgtgt	78514
rs241861594	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77427968	AAAGAATGGAGTCTG[C/T]CCTTCCCTACACTGC	78514
rs241861712	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77297197	AAATTTGAACATACC[-/T]TTTTTAATTGATTTG	78514
rs241869963	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77413785	TTGATATCCGAAGAT[A/G]ACAGAGTGTAAAACA	78514
rs241871090	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77288546	TCACTGCTCATCCTA[A/G]AATCAGGCTGTCAGA	78514
rs241871128	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77500721	GCTTTAGGTGGATTC[A/G]GGGAGCAGATTCAGG	78514
rs241872285	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484248	CCCATGTCAGGGACT[A/G]AACACGGGGCCTCAC	78514
rs241882344	in-del	-/TTGTT			intron-variant	Arhgap10	Mm_Celera	8:77447104	TTTGTTTGTTTTGGG[-/TTGTT]TTATTTTGTTTTGTT	78514
rs241888360	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77385903	GATAATCCTTGCACA[C/T]AGTGAATGCATCTGT	78514
rs241890409	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77470862	AGAAGGAGATGTCTG[A/G]TCCTCGAGAACTGGA	78514
rs241921183	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77333440	TACCCTACCCATTCA[G/T]TTGAAACCGAAAATG	78514
rs241925643	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77338380	TTGGGTCATAATGGC[A/G]AGGAGAAGAGACTGC	78514
rs241929299	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77418019	TAGAATAGAGAGAGG[A/G]TTTGGGGCAATTCCT	78514
rs241930193	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77506208	CTTCTTTAGCACCTA[G/T]AGATTACATGTTATT	78514
rs241934792	in-del	-/AA			intron-variant	Arhgap10	GRCm38.p3	8:77277467	TTTGTTTGTTGTTTG[-/AA]AAAAAAACAAAACAA	78514
rs241937370	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77410642	AATGACTTTATGAAA[A/C]CTCTGCGTGCCTAAC	78514
rs241955494	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77280861	GTTCTCACCTAAGCT[A/C]GTGTGTTCAGTGATT	78514
rs241955505	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77289280	CTTTATTCCCATGAA[C/T]ATTGACAGAAAACTC	78514
rs241956493	in-del	-/TCAC			intron-variant	Arhgap10	Mm_Celera	8:77461568	GACTGCCCTCTTCCT[-/TCAC]TCCCTGACACTGGCT	78514
rs241964942	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77476482	CACTCTATGCAAGTG[C/T]TAAAATGGTCTATCA	78514
rs241970226	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77454496	TTGTCGCCTAGCAGT[C/T]ACAGTAAACTAAGAT	78514
rs241975662	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77354108	AATGGTGCAGCTCAC[G/T]TCGAATCAATTATAC	78514
rs241979751	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77339187	CTGTGTGCCCTGGGG[C/T]CTAAAGAGACTACAA	78514
rs241981471	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77332901	GGTTCGGTGACAATG[G/T]GTACATAGTAGGCAT	78514
rs241988507	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77261146	TTTAACTCGGCTGTT[C/T]CCACCACACACATGT	78514
rs242003037	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77478224	TAATGCAGGGCATTT[A/G]TTAGCCATTGCTCAA	78514
rs242006240	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77424159	GCATAAAAATCCTCT[A/C]TGAAGTAATTGAAAG	78514
rs242008521	snp	A/C			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484798	TGAGACTGTCTCACA[A/C]AAAGGGGAAGAAGGG	78514
rs242024921	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77320554	GACACAAGGACACAG[A/C]CAAAGCTGAGAGGCA	78514
rs242031282	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77326269	ACTGACTGATTAAAA[-/G]GGGGGGCTGAAGAGA	78514
rs242035932	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77397147	CTCGATAATGGAAAA[A/G]GTTGCCAAAGAACTT	78514
rs242037397	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77410567	GCTAGCTCACGGCTA[C/G]CTCACATTCACAGGG	78514
rs242048517	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77467346	ACACCACAAAAAGCC[A/G]GACAGTGGTGATACA	78514
rs242062076	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77510646	AGGACTCACAGGTGC[A/G]GGCCAGGACCGCCCA	78514
rs242065694	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77497086	AAAAAAAAAAAAAAA[A/C]AGTTCTGCCACAGAA	78514
rs242068702	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484246	GACCCATGTCAGGGA[C/T]TGAACACGGGGCCTC	78514
rs242085694	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77321045	TCTGAGATGAACCAA[A/G]AGAGAAACTGAGGTA	78514
rs242088596	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77455194	AACCTGGAGGCAGAA[C/T]TGAAGCAGAGGTCAT	78514
rs242094555	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77384074	GAGCGAGCGCATGCT[C/T]TAGCTGCAAGGCCAG	78514
rs242098837	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77397916	GGCCGAGCAGCACCC[A/G]CCACAGTCTAAGCTT	78514
rs242109084	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77422688	GGTGGAGGTGAAGGT[A/C]CTTGTGTCTGAGACC	78514
rs242112273	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77293810	ATGAGTTTGTTGAGT[G/T]GGGAGGGTATAAAAA	78514
rs242114909	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77497205	TGCTGTATCTGGAAG[C/T]CAGAAGAAAGAAGTG	78514
rs242123031	in-del	-/A			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494102	CCTACATTCTATGAT[-/A]AACAAATATTACTAT	78514
rs242131131	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77415469	CACTGGCTAGCATAT[A/G]CATATACAATGGAGC	78514
rs242135479	in-del	-/CTGCCT			intron-variant	Arhgap10	Mm_Celera	8:77499016	GCTGCCCGCTGCCCG[-/CTGCCT]CTGCCTCTGCCTCTG	78514
rs242138673	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77287461	AGGGTGATGGGAAGA[A/G]CTGTGAGGCCTACTG	78514
rs242143136	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77382187	AGAGAAATTCTAAAT[A/G]CACAAAAAAGACAGA	78514
rs242149859	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77305901	CAGAAACCAGTATTC[A/C]CACCACAGTGAGCCC	78514
rs242155433	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77252653	CTTATGCCTTTCCCA[C/T]CTCAGGGCAGGGCCA	78514
rs242164075	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77337817	CCACCCTCCCTTATC[A/G]CAGCCCTCCCACCCT	78514
rs242191238	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77501924	AAACCCTGACGGGAC[A/G]GATCCTAGTAGCAGA	78514
rs242198255	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77327514	GCTCTGGGAAATCCC[A/G]GAGTGTCTTTCACAC	78514
rs242206112	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77366924	AAATTTCTAGTTCCA[A/G]CCTGTGTTTAATTCT	78514
rs242214578	in-del	-/AG			intron-variant	Arhgap10	Mm_Celera	8:77447378	ACAGCCAGCTAACAG[-/AG]TCTCTAGGAACCGAG	78514
rs242218358	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77423570	AAACAGCATAGATTC[-/T]TGGGTAGTATCTGCC	78514
rs242228204	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77452718	CCCGTCAGTCCAGTC[A/G]TATTTGTGTGAATGC	78514
rs242235662	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77510634	TCAGCCTCACTCAGG[A/G]CTCACAGGTGCAGGC	78514
rs242237301	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77409822	CCGTAAGGATTGACC[G/T]GAAACCTCACTATAC	78514
rs242243424	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77435855	CTATGACCAAGGTAA[C/T]TCTTATAAAAGCAAC	78514
rs242248020	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77266433	AGCTGACCCCTTGCT[A/G]CTTGCTGCTACATTT	78514
rs242250262	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77284401	GCTCCAGCGAGGGGG[A/G]AAAAAAAACGCAAAG	78514
rs242265342	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77364284	ACAACACCCAAGAAG[C/G]AGCGCTACCCAAAAC	78514
rs242266274	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77367569	ACTGAGGGGAAAGGA[C/G]AGCACACCCCTATCC	78514
rs242266542	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77508978	AAACACAGAGTAAGA[C/T]TTTCTTAATTTAATA	78514
rs242266747	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77272018	GCAAAAGCCCCAGAA[A/T]TCGCATTCTGCCGCA	78514
rs242281361	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77321583	CAGTCACTGTGTTGA[G/T]TCTAGATTACACAGA	78514
rs242297487	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77458508	GTTACTATGCACACA[A/C]AACCCATTAGACAGA	78514
rs242311271	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77405109	CCACCTTCCACAAGG[C/T]ACTACATCTGTTAGC	78514
rs242314484	snp	C/G			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77516588	ACAAATGGAATAAAC[C/G]CCCAGAGATGGAGAG	78514
rs242316296	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77478747	CTGTAAAGACTGGCT[C/T]CCTAGGCCGAGCACA	78514
rs242317562	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77501319	GCCAGCCCTGGCCGC[C/T]TCTTCCCAAGTCCAA	78514
rs242320188	in-del	-/CAAT			utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250696	AGAATTAAACATCAC[-/CAAT]AATGCCCAGTCCTGC	78514
rs242322976	in-del	-/CGCC			intron-variant	Arhgap10	Mm_Celera	8:77277718	TGTGCTCTATTGCTG[-/CGCC]CCACCACCACCCCCA	78514
rs242325589	in-del	-/GGG			intron-variant	Arhgap10	Mm_Celera	8:77474540	TTTTATAAATGAACT[-/GGG]GGGGGGGTCATGAAA	78514
rs242326834	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77266890	TTCCAAAATGGGACT[C/T]GAAAGCCAGCGTCTT	78514
rs242327087	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77260430	TAAAAAAATGGTTCC[A/G]TGGTTAAGAGGCTTA	78514
rs242330832	in-del	-/TGA			intron-variant	Arhgap10	Mm_Celera	8:77346237	GAACAACAGCAGCAC[-/TGA]TGAGGGAGAGCTGAT	78514
rs242335484	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77275812	GTTGGGCCTGAATGT[A/G]CAGTGAGTTGAGCAA	78514
rs242336182	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77357868	TACGTAGTGTATAAT[A/G]GAAATATTCTGCATC	78514
rs242339149	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77408082	CTTTATCATTAAAAA[-/G]AAAATTAATCCTTTA	78514
rs242344206	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77260403	TTGGGTCATTCCTTA[-/G]AATTTAAAGTGTAAA	78514
rs242364321	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77338598	GCTGACTCCTAGCAT[C/T]CTTTCCAGTTGTCCT	78514
rs242367124	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77345082	TGCTGGTATTCTGAT[A/T]CACTTCATGCCTGAG	78514
rs242367318	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77410134	AGCAAACTCAGGCTC[A/G]AAGCCAATGCTACAA	78514
rs242378288	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77449681	CACTCAGCTAGGTAC[C/T]ACCCGGGAGATCCAA	78514
rs242389059	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77314065	TGGACATAAGCCCAT[A/G]GGTGATGCTCTGCTT	78514
rs242389666	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77427995	CTGCACATAGGAAAA[-/G]GGTATAATAAAAACT	78514
rs242394553	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77257775	GGGAGGGAGTTTCCC[A/G]GGGAGCCCACATATG	78514
rs242397199	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77292214	ACACTGTACTCCTTC[A/C]TAGGCAGGCTCACAG	78514
rs242401487	in-del	-/AT			intron-variant	Arhgap10	Mm_Celera	8:77326451	AAATAAGTAAATAAA[-/AT]ATATATATGTGTGTG	78514
rs242404060	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77420299	TCCCTGTCTGTCACG[-/C]TCCTGAAATGAAAGT	78514
rs242417737	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77387327	ATCATCTGGACCTGG[A/C]GTTACAAGGTGGTTA	78514
rs242421452	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77436056	TTCCTCACTGGGAGA[A/G]GCCTAAGCATTGGAG	78514
rs242421847	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77339277	AAATACTTGAGCAAA[A/C]TGAAATATCACGTGA	78514
rs242454627	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77257677	TGCCAGGTGGGCTGT[C/T]CTTTCCCACTGCTCA	78514
rs242454947	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77295691	TACCTAATAAAAATA[-/T]TAAAAAAATTAAACT	78514
rs242456936	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77372263	AGCCCTACCTGTCCC[A/T]GGATCTCAGCCGTAG	78514
rs242463502	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77336710	TCCACAGCCAAGTCA[A/G]TGATATGGACGTGAG	78514
rs242468244	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77475280	AAGAGCAGCCCAGAC[A/G]GAACATGGCAAGTTC	78514
rs242468265	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77481587	CTCAGACGCAGCTTA[G/T]CAACAGAGCACACAT	78514
rs242477490	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77388032	TCCCGAACCCCATAC[A/G]AGATCTGCCAGACTC	78514
rs242480311	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77435453	CTACGGTCTGGATCT[A/T]AACAGCCTCCAAAGG	78514
rs242500126	in-del	-/AAAAA			intron-variant	Arhgap10	Mm_Celera	8:77284399	AGCTCCAGCGAGGGG[-/AAAAA]GAAAAAAAAACGCAA	78514
rs242506375	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77449747	AGCTCAGAGCTCCAT[-/C]CCCCTACTTCACAAA	78514
rs242515894	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77372675	GTACCCAGCACAGAC[A/T]GACTCACACTGTCCC	78514
rs242517259	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77417673	CAAGAGAATAAGATG[-/A]AAAAAAAAAGAGAGA	78514
rs242520615	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77282501	CCCACAAAGGGCTGC[A/G]CCCTCCCTGCTGTCA	78514
rs242526192	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77481095	TGAAATGGTGGCCCA[A/C]TGTCCACGCTGACTG	78514
rs242528870	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77425274	GGGAGGAAAAAAGTC[-/A]AAAAAAATTTAGAAA	78514
rs242532526	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77381592	GTGTGGCTCCAGGAG[A/G]AGTTAGGAGTGTGGC	78514
rs242536330	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77330966	ACGTCACAGAGCTGT[A/G]TGAAGATTAACTCGA	78514
rs242586312	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77416804	AAAACACAGCAAATG[A/G]GAATCTCTGGACTCC	78514
rs242588284	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77377493	TATATATGCTACATG[A/G]AAATATTCATTCTAA	78514
rs242589265	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77382018	TATTAGAGTAAGTTG[A/C]GTGTGTACATAAGCT	78514
rs242595175	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77460400	GTACAAAGTAGCAAT[A/G]TTAGCAAGAAAGAAA	78514
rs242600710	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77283794	ACAGACAGCCAACAT[A/G]TAAGAGCCAGGGAAT	78514
rs242615856	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77288746	CAGACTGAAATGGCC[A/G]GAGAACTGCGGCATA	78514
rs242624475	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77345051	AACCAGTCTCCTCAG[C/G]TACAGGCTCCTTCCA	78514
rs242641033	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77263587	ATCCTTCTCCCTGGG[C/T]CTCTTTATGCCTCTG	78514
rs242645309	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77363211	ACATGCATGCACATA[C/T]AGGGGTCAGAGGTTA	78514
rs242648803	snp	C/G/T			intron-variant	Arhgap10	Mm_Celera	8:77460166	AAATCCCAAAGGAGT[C/G/T]GGGGGTTGGGGAGCA	78514
rs242649204	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77466207	AAAAACTGTGTGTGT[A/G]TGTGTGTATGTGCAC	78514
rs242684553	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77364098	GAGCCCACTAATGGT[-/A]AAAAAGGAAAATATG	78514
rs242685056	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77507060	ATGACGTAGTAGACC[A/G]TTCAGTGGGCAGAGT	78514
rs242688320	in-del	-/GT			intron-variant	Arhgap10	Mm_Celera	8:77413674	ATCTATGATTTTTTT[-/GT]GTGTGCATACATTTT	78514
rs242704780	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77264261	CCTATGCTGGGCAAG[C/G]CCAGACCACTCACCC	78514
rs242708913	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77465220	GGTGTGTTCAATGGA[A/C]CAGGCAGACAGAGTG	78514
rs242713213	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77287681	GGCGTGGTGGTGCAC[A/G]CCTTTAATCCCAGCA	78514
rs242726800	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77325889	GAACAACAAAACCTA[C/T]TCCTGTGTGATGGAA	78514
rs242745966	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77415166	TCCTACAGGTGTCCA[A/G]CTAGCCAGCAGACCT	78514
rs242776877	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77452539	GCCAGACGTGGTGGC[C/G]CATGCCTGTATCCCC	78514
rs242776917	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77474954	TCTCTATGATATAAT[-/AA]GAGAGGGTAGAGTAA	78514
rs242779922	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77475779	ATACACAACTGAAAG[A/G]TCAATACATGTTTGA	78514
rs242787830	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77326376	CTCACAACCATCTGT[A/G]ATGTGATCCGATGCC	78514
rs242790086	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77320168	AGCACTTGGGAGGCC[A/G]AGGCAGATGGATCTC	78514
rs242793410	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77462895	CTCTGAGAAGGTAGC[A/C]AAGGGTCTAAAAATC	78514
rs242831263	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77421418	CCCAGTCAGGGCTTC[C/T]GCTTGGCTAGGCACA	78514
rs242833496	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77495700	GACAGTGGGTTCCTG[C/T]TTGATTCTGCTCAAA	78514
rs242835225	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77386518	TAATGAGATCTGATG[C/T]CCTCTTCTGGTGCGT	78514
rs242847661	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77305679	TCCAGTTTCTGTCTG[C/T]ACCCTGGAGCTGACC	78514
rs242850184	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77320690	TCAGTGGTGTGCCAC[C/T]CCCAGTGATCCGCAT	78514
rs242858554	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77386847	AGAGAAAGAGAGAGA[A/G]AGAGAGAGAGAGAGA	78514
rs242862391	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77376043	TCCCAGCACGACTTG[-/A]AAAATCAGCTATTGC	78514
rs242872352	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77377828	ACAGACACAGACACA[C/G]ACACACACACACACA	78514
rs242884094	in-del	-/CACCC			intron-variant	Arhgap10	Mm_Celera	8:77337167	AGAGATCCCAGGAAA[-/CACCC]CACAAGCGGGGAAGC	78514
rs242886816	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77432349	AGAGTCAGGAAAATA[A/T]GTCCCAGTAGCAATA	78514
rs242900714	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77369680	AAAGACATAAAGTAA[A/T]CATGGCCGGACCTCC	78514
rs242916225	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77441931	ACTTAACTAGGTCTC[G/T]AAACAAGGTTTCTAA	78514
rs242916907	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77331841	GGGTGACATGGGACT[G/T]ACTCAGCCTGTCAGC	78514
rs242917196	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77381103	TGCTGCTGGGATCAA[A/G]CACTGTGAACACAAA	78514
rs242922628	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77290580	CACAAACTCCAGGCC[C/G]ACTGAGACAGTGTAG	78514
rs242942556	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77439526	AGAATACTGCCTATA[A/G]CCTAGGCTCAGATTT	78514
rs242946792	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77431312	TGTAAGGGATGGCTG[C/T]TTGTGCATGGCTCTG	78514
rs242955960	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77441976	ACCTCTCCCTCTGTA[A/G]CCAGTCCATCATTTA	78514
rs242958679	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77362833	CATCTATTTTGTCAA[A/G]AGCTAAGGTTTCCAT	78514
rs242970831	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77371153	ATAGAAATGACTCAT[A/G]GAAAATGTGTCTCTC	78514
rs242988374	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77325961	AGATCCTTTCCAGCC[C/T]GTGCTCACTGCTCTT	78514
rs243003944	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77486017	ATAACTGTGTGCTTA[-/G]GGGGTCACCAGAACA	78514
rs243005293	in-del	-/A			intron-variant	Arhgap10	GRCm38.p3	8:77480750	GTCTCCTGTAAGAAC[-/A]AAAGGTTCATAACTA	78514
rs243023086	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77271032	TTTTTGCTCTGGGGA[C/T]CTGCAAATGCCCCAG	78514
rs243026526	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77447874	TACATCTTGATCCAC[A/C]GTCAGCAGAGGTGAC	78514
rs243032072	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77408851	CCATTCTTGGCCAGA[A/T]CACATAAAGAAAGCA	78514
rs243039109	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77283881	GTAGCAAGTGATGAG[C/T]TGGGATTACTGGAAA	78514
rs243044901	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77433337	ACGAATGGGGTGCAG[C/G]GGGAGGCCAAGAGGA	78514
rs243057011	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77362777	TCAGAATGAAAGGAG[A/T]ACCGTAAGAGAACTC	78514
rs243059009	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77341043	ATGTTTAGTTTCCCC[A/C]AATCACATACAGCTA	78514
rs243067306	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77496152	TAAATAGAAATAACG[-/A]AATGCCACGACATGT	78514
rs243068491	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77415631	TTTCTTTATGTTAAT[C/T]ATAAATTAGGGTAGA	78514
rs243069280	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77475162	AGGAAGGGGGGATTC[A/G]GTAGCCCAGCTTGGG	78514
rs243097756	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77463143	AACTGTGACAATATA[A/C]ACATATACTTTGGTG	78514
rs243101980	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77351030	CCCTCACACTGCAGG[C/T]ACACAGTGCTGGCAC	78514
rs243106993	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77318729	CCCTCCTGCAATCCC[A/G]GTCCTTATGCTTCAA	78514
rs243110779	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77456827	ACAGAAAATGTGGTA[C/T]ATTTACACAATGGAG	78514
rs243111801	in-del	-/TTTA			intron-variant	Arhgap10	Mm_Celera	8:77414769	TTGTTTATTTGTTTG[-/TTTA]TTTATTTATTTGTTT	78514
rs243113455	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77398981	CTGCCCTTTCCTTAA[C/T]GTACTGGGTTAGAAC	78514
rs243125975	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77264435	AGGAAGAGAGAGTAA[A/G]TACCATCACCCTCCG	78514
rs243129046	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77356575	GAGCTCAGCCATTCC[A/G]ACCCTCCTCCAAACC	78514
rs243130070	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77513337	TGAACAAAACCAGGA[C/T]CGACAGAAGGAAAGG	78514
rs243142777	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77481064	TGGCCCACTGTCCAC[A/G]CTGACTGTCTACACA	78514
rs243142996	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77447056	GGTTTGGTTTGGTTT[-/A]AGGGGGGGAGGGTTT	78514
rs243143860	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77480807	TCAATTTTCAAAACA[A/T]CAGAAAACAAGTTTG	78514
rs243145647	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77488084	CTGCTACCAAGTCAA[A/G]CCGGCCTGGGATCAA	78514
rs243147011	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77474985	ACCTACACAGCTGCA[A/G]TCCCAGCCCAGGGAG	78514
rs243153618	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77380913	GTCTACCATTAGCCC[A/G]ACTGTGCAGACTGAA	78514
rs243157389	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77297574	AAACCAAATACTGCT[C/G]TGCTAAGAGAACACA	78514
rs243171573	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77444058	TAAGGTGCCTCTGGG[C/T]TCCCCTGGAAAGCTC	78514
rs243172609	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77399603	TTCTTAAATCTGTAC[A/T]TTTGTGACTATGTTC	78514
rs243173064	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77436784	TTTCTCCCATGACCT[A/T]CCAGACACTTCCAAT	78514
rs243188639	in-del	-/AGTAACAC			intron-variant	Arhgap10	Mm_Celera	8:77405595	AGTTTGCGTCACAGG[-/AGTAACAC]AGTTTGGGGTGAGAA	78514
rs243197462	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77486834	GCTGTTTCAAGCCAA[G/T]GTTGGCCTGCTCCAT	78514
rs243199189	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77252450	GCCCTATTCTTAAAG[A/G]TTCTATCCATACATT	78514
rs243204360	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77511802	ACAAACCAAAAAAAA[-/C]AAAAACAAAAAAAGA	78514
rs243213631	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77431168	CTTCTCTGGTTCTTA[C/G]AGAACTGTTATTAAC	78514
rs243217528	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77340937	CACACACACCAAAGC[A/G]GACACAGTCTTCCCA	78514
rs243226401	in-del	-/TG			intron-variant	Arhgap10	Mm_Celera	8:77354432	ACAGTTTTCAGGGGT[-/TG]TGTTTCCAAGCACAG	78514
rs243235528	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77473854	TTCTTATGAAGTACA[C/T]GAAGCAAGCTTAGAC	78514
rs243235950	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77297538	TGACCTGAGACTATA[C/T]TTGGCCATGTGCCTA	78514
rs243244080	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77379809	CTACATTTTTTATTT[G/T]AGCTCCTGGAATAAT	78514
rs243273556	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77432856	AGCGTTAGGAAAAAA[-/G]CGGCGTCTCATTTTC	78514
rs243275106	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77438661	CGCCCTTTCTGAGAC[A/G]ATCAGAAGGCCACTC	78514
rs243288464	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77370121	GGGGGGGGGCGGGGG[A/G]ATAGGAAAGAGGGGT	78514
rs243291442	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77280817	GGATGGAGTCAGATC[A/G]TTGTGTTTGCAAGTA	78514
rs243294631	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77296831	TTGAAAACTAGACAG[-/C]TTTAGAAGGCACTCT	78514
rs243304598	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77506681	TGTTGACTGTGGTTA[C/T]AGGATACATCCGGTT	78514
rs243306623	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77479840	CACTGTGCAAGTGTG[C/G]GCTGTCAGGCTCAGA	78514
rs243317480	in-del	-/GT			intron-variant	Arhgap10	Mm_Celera	8:77424947	TTGTGTGGTGTGTGA[-/GT]GTGTGTGTGTGTTCT	78514
rs243326752	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77340035	AAACACTGCCATCTG[A/G]CTGTGTCCCCATGAA	78514
rs243328070	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77347695	ATGGAAGAACGCTAG[A/C]TTTGGAGCCTACCGT	78514
rs243335050	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77404227	GACAGCTGGACACAC[A/G]GATGCAACATTCCAG	78514
rs243335055	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77464369	GGAAGTGTCACCATC[G/T]TAATTACCGTGTGGA	78514
rs243345647	in-del	-/AAA			intron-variant	Arhgap10	Mm_Celera	8:77441013	ACATAGACACAGGGG[-/AAA]AAAAAAAAAAAAGGC	78514
rs243348236	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77268947	GTCATACTCCACAGC[C/T]GCATGGCTTACCACG	78514
rs243360390	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77356359	CACAGGGCACACAGG[C/T]ATCCATGAGGTAAAA	78514
rs243368370	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77513667	TCGGAAGGAGCAAGG[A/T]CCTCTCCTTGTATGT	78514
rs243379575	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77269583	TAAAAGAAAAAAAAA[C/T]TATCTCCTCCCTAGA	78514
rs243382987	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77269483	GCCTGCTCCTCCACA[C/T]TTGTCTCTCTGAATC	78514
rs243390302	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77411519	ACACATACACATGCA[C/T]ACACGTGTACACATA	78514
rs243408153	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77428358	TAAAATTGCACACAT[-/G]AAAAAAGTGAGATAT	78514
rs243413924	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77311981	TCACCTAAAAATTAC[C/T]CTACACCAATAAAAA	78514
rs243414818	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77317253	AGCATCAACTCTGAC[C/T]GAAATGTCCTATCTC	78514
rs243434640	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77499986	CACAGTCTAAAGGAT[A/T]GGACCACAGAACGCA	78514
rs243438511	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77322055	TGCAGTCTCTTGAGT[C/T]GGGCATCACAGCCAG	78514
rs243442659	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77438317	CACTCCCGTCCCTTC[C/T]CCCTTTTTATCAGAT	78514
rs243449529	snp	A/C/G			intron-variant	Arhgap10	GRCm38.p3	8:77412025	TGAGCAAAGCTAAGG[A/C/G]TCAGAAGGAGGGAAA	78514
rs243456221	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77481254	AATGACGGCCCACTG[A/T]CCACACTGTCTACAT	78514
rs243460697	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77263729	TTTCATCCATCAAAT[A/G]AGACTCCTGTTTCTT	78514
rs243462630	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77270051	TCAAGTCAGGCACTC[A/G]GAAGAGGCCAGCAAA	78514
rs243462753	in-del	-/TTTA			intron-variant	Arhgap10	Mm_Celera	8:77474191	TCAGTCGTTAGCACC[-/TTTA]TTTAGTATTTATGAC	78514
rs243462968	in-del	-/TTTTT			intron-variant	Arhgap10	Mm_Celera	8:77486352	GCCTGACAGCAACTC[-/TTTTT]TTTTTTTTTTTTTTC	78514
rs243474604	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77261955	CTAGACATAGGGAGC[A/G]AATGGATTAAAGGAT	78514
rs243478683	in-del	-/TCTCTCTCTC			intron-variant, downstream-variant-500B	Arhgap10	Mm_Celera	8:77358151	CCATCTCAGACCCTT[-/TCTCTCTCTC]TCTCTCTCTCTCTCT	78514
rs243492759	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77316258	AAAACACCTTCAGCT[C/T]TGATTTACAAGTTTA	78514
rs243497860	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77437443	AGGACCCTGGCTGGT[A/G]CACACAAGTCAGCCA	78514
rs243508840	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77323309	CCCAATTTCACACAC[-/A]TGAACTCCAGGCCAA	78514
rs243514768	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77251495	GGCCTGCTTCAACCC[A/C]TCAAGCACTACCGGA	78514
rs243524629	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77426555	GGGCGCGAATCATGG[C/T]GGAGCTTCTGAGACA	78514
rs243528999	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77499877	AAAACTAATGCTCTA[C/T]AATCATGGGGGAGGG	78514
rs243537205	in-del	-/ACACACACAC			intron-variant	Arhgap10	Mm_Celera	8:77415388	GCAGGCAGACTTGGG[-/ACACACACAC]ACACACACACACAGA	78514
rs243549325	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77469599	TCTCAGCAGTTAAGC[A/G]CACTAGCTCCCGAGT	78514
rs243551655	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77399655	CACTTCCTAACTCAC[A/G]TTAAGATGGGGACCA	78514
rs243552033	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77439157	GGTTGCAATGAGCTC[A/C]TAGCAACAGCTAGAC	78514
rs243554218	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77317220	AGGCCTTCCTCGAGG[A/G]AAGCACCCCTTAAAT	78514
rs243574555	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77408078	CTAGCCTTTATCATT[A/T]AAAAAAAATTAATCC	78514
rs243574648	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77380808	ACAGCAACTGAAGAG[-/A]AAAAAAATCAGGTCG	78514
rs243583643	in-del	-/TGAA			intron-variant	Arhgap10	Mm_Celera	8:77468050	CAAGTCCCTTACAGT[-/TGAA]GAGAGATGACAGGAA	78514
rs243597939	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77374381	AGATCGGTCCTGGCC[A/C]ATTCAGCTGCTCACA	78514
rs243600530	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77361634	AATAGCAAAGTCCAG[C/G]AGACCAGACATGCTA	78514
rs243610203	in-del	-/AAGAACAGAGCTGCACACACACATAAAGAACATAAAGAACATA/TGCACACACACACAAAGAACATAAAGAACATAAAGAACAGAGC			intron-variant	Arhgap10	GRCm38.p3	8:77402985	AACTCTTTCAGTCTG[lengthTooLong]AAGAACAGAGCTGCA	78514
rs243612699	snp	A/C/G			intron-variant	Arhgap10	GRCm38.p3	8:77445787	GCCACGTGGAGTACT[A/C/G]GGAGAGCTCGTCCCA	78514
rs243613007	snp	A/G			intron-variant, utr-variant-5-prime	Arhgap10	GRCm38.p3	8:77492233	TGAGCCACCATGGCC[A/G]GTTTCTGTGCTACTG	78514
rs243616991	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77285596	GGAGAGGGAGTAACC[C/G]AAACAATCCAGACGC	78514
rs243643284	in-del	-/AAAA			intron-variant	Arhgap10	Mm_Celera	8:77319249	AAAAAAGAAAAAAGG[-/AAAA]AAAAAAAAAAAAAGA	78514
rs243651955	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77403153	CTCAGAAAAGTCACA[C/G]AGTACAAGCTCTGAA	78514
rs243652252	in-del	-/TCTT			intron-variant	Arhgap10	Mm_Celera	8:77480574	GCCACCACACCTGGC[-/TCTT]TCTTTTTTTTTTTAA	78514
rs243652932	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77286297	CCCACCACAGATACA[C/T]GTACACAGATTGCAG	78514
rs243657238	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77374787	TAAGGCTCACATGCA[A/G]ATGGACAGTTGTTCC	78514
rs243658297	in-del	-/CTGCTG			intron-variant	Arhgap10	Mm_Celera	8:77253051	GGCTATTTTTGAGTA[-/CTGCTG]CTGCTGCTGCTGCTG	78514
rs243671615	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77355038	AAGGGAGGGACTGTG[A/G]GGAGGACACTTCAAT	78514
rs243679779	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77384975	CTACACCTGGAATTT[C/T]CAGATAGAAAGGTTT	78514
rs243685141	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77498863	AGTTTTTTGAGACAG[G/T]GTTTCTCTATGTAGC	78514
rs243693983	in-del	-/CAAGG			intron-variant	Arhgap10	Mm_Celera	8:77290299	AGTTAACAGGTAGCT[-/CAAGG]CACCATCCCTACCAC	78514
rs243694124	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77268528	CAGCACAGCACAAAG[A/G]CGTGAGTTAGACATC	78514
rs243696378	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77267905	CAGAGGTCATCTCCG[-/T]TGCTGCTTGGTGGGC	78514
rs243699357	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77355401	AAGAAACATAGAGGA[C/G]GGGAGGGGAGGAACC	78514
rs243702679	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77505679	CATGAAATGCACAGT[-/C]CCCCCCGAGACACAG	78514
rs243704058	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77410971	TACTAAAATGACAGA[C/T]CCAGCAAGTATTTCT	78514
rs243710257	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77462958	TTCCAGGGTGGCCCA[A/G]TGGACGTTAGAAGCA	78514
rs243723249	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77483503	TTAAACACCTAAGAA[A/G]CTGAGTCTGTAATGA	78514
rs243740417	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77254787	CAGCCTTGGGTCTCA[G/T]GGATGTTAAGTGTCG	78514
rs243757154	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77355991	TACCAGCCATTCTAT[A/T]CTTATCCCACCCACT	78514
rs243757212	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77510934	GTCAGATTTCCAGGA[-/G]GTACCTGTGCACTTG	78514
rs243766439	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77258454	TCAGCCAAGGCCCAG[A/G]GTGACTGACTTGCTT	78514
rs243773638	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77468940	AGTAATGAAAATAAT[A/G]TTATGGCTGGGTGTC	78514
rs243775612	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77462651	TGATAGCTTTCACTG[A/T]GGAGGTCTTTGCTCT	78514
rs243776395	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77412309	GTGTGTGTGTGTGTG[C/T]GCACACGTTCATGGA	78514
rs243803822	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77334127	GCACACACCTTTAAT[C/T]CCTCTGGCTGGAATA	78514
rs243814498	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77251169	CTGGCCCTCAAAAAC[C/T]TCCTTATCTAGTACC	78514
rs243820418	in-del	-/GT			intron-variant	Arhgap10	Mm_Celera	8:77509005	AATATATATATACAC[-/GT]GTGTGTGTGTGTGTA	78514
rs243821130	in-del	-/CACAACACACAGATG			intron-variant	Arhgap10	Mm_Celera	8:77475742	ATACATACAGTGCAA[-/CACAACACACAGATG]CACACACATACACAA	78514
rs243822428	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77348953	CGGGTCCATGCTCAC[C/T]GCTGAGACTCTACAG	78514
rs243825550	in-del	-/A			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493200	GAGGAGGAAGAGGAG[-/A]GAAGAGGAAAAAGAG	78514
rs243834397	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77468183	GAGGCACAACCTCAC[A/G]CAGGGATACAATGAA	78514
rs243841586	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77460310	CACTCAGCCTCCAGA[C/G]CCATTTATTACAATG	78514
rs243845417	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77259534	CCCTGACTTCCCTTC[C/T]ATGCTGGGCTACATC	78514
rs243854905	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77407979	CCAGATATAGGGTAC[A/G]AGTCTATTATCCTAG	78514
rs243869957	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77321686	TTTTTACTTAATTCT[A/T]TTTTTTTTTAATGAC	78514
rs243870728	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77396011	TGTCCATCTATACAA[A/G]ATTTATTCACAGCCT	78514
rs243871129	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77279082	CCCTGGGCTGCACCT[C/G]CTTGCAAAGTCTTGT	78514
rs243877940	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77429620	AATTCTGGCAACTGA[A/G]GGAGAGAGGCCTAGA	78514
rs243878466	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77292147	TCCAAGATGCAACAA[A/C]AGTCATTTGAACAGG	78514
rs243886570	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77328456	TCTTAGTTTTAGCAA[C/G]CTTCCTTACAAACCA	78514
rs243890397	in-del	-/A			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484883	CAGTAACTTCTTCAG[-/A]AAGAAAACTACTTGA	78514
rs243892113	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77361518	TCCAACAAAGTAAAT[A/G]AGAAAATATTTTAAA	78514
rs243893837	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77509539	AATAGGGAACCAAAG[G/T]AGAAGAGTGCAGCTA	78514
rs243914288	snp	A/G/T			intron-variant	Arhgap10	Mm_Celera	8:77292897	GGCTTCAGAGGAGCC[A/G/T]CCCATGCAGAGGCGG	78514
rs243919709	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77272643	TTTCCCCTCTTTTTT[C/T]GCTATTTCTCTTCCC	78514
rs243921904	in-del	-/ATGGGT			intron-variant	Arhgap10	Mm_Celera	8:77343081	CTCCCTGTGGATGGA[-/ATGGGT]AAGCATAGACATACA	78514
rs243945826	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77423998	AGTCACCATCTCCAG[A/G]GCTTTCAAAGAGGAA	78514
rs243947679	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77329302	GTGGTGGGGACAAAG[A/C]TTTGCCTCTCTCAGG	78514
rs243971045	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77444820	GATTCCCTCTCAAGA[C/G]GGACGCAGCATTTCA	78514
rs243983575	in-del	-/TGGGTGGTACCATCCC			intron-variant	Arhgap10	Mm_Celera	8:77258098	GGGCCTAGCCCATGG[-/TGGGTGGTACCATCCC]TGGACTAGTAGTCTT	78514
rs243984171	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77364750	CTGACAGATGACAGT[C/T]TGCGAAACTAAAAAT	78514
rs243988258	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77271014	CTAGGCACGCAGGAA[A/G]CATTTTTGCTCTGGG	78514
rs243994831	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77325480	CTGCCCAGTAGGAGC[-/T]GCTCTCCAGTCTGCT	78514
rs244022002	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77265097	AAAAACAACTTAAAA[C/T]TCACAGCAGAGAAAC	78514
rs244026493	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77339558	TAGACCTTAGTGCAT[A/G]ACTATGGGTTCAATG	78514
rs244032084	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77446078	ATACCACAGGCATTG[-/T]TTTTTTTTTCCTTCC	78514
rs244035608	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77464310	GTGTGGATTCTGCCT[A/G]ATGGAGAGCCCTGAG	78514
rs244039428	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77286671	ACCAAACATTCAAAC[G/T]TATTAGCTTACAGAG	78514
rs244049054	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77444934	GAATTACTGAGCGCA[A/C]AGGCTTTTGACCACT	78514
rs244050526	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77351687	CCTGGAAAAAAAAAA[-/G]AAAAAAAAAAAAACA	78514
rs244051632	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77293725	ATCTGACACCATGTG[C/T]TCATCCTTAGAAACA	78514
rs244053324	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77286906	TTGTAAGGCACAGTT[-/AA]AAAAAAAAACCCAAA	78514
rs244084416	in-del	-/ACACACAGC			intron-variant	Arhgap10	GRCm38.p3	8:77254194	TCCAGCTTTCAGAGA[-/ACACACAGC]ACAGACCTTGTGGTA	78514
rs244088079	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77294163	ACCATAACTGTGATT[A/G]ACCAATCAGCTTGAA	78514
rs244091120	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77253384	GCTCCCCTCTCCAGC[A/G]CTGGAATGGTGTGAA	78514
rs244091987	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77463715	ATCAGCATAGACTCC[G/T]TGGGCCTATTAGAAT	78514
rs244098614	in-del	-/AG			intron-variant	Arhgap10	Mm_Celera	8:77263228	AAAATAGTGGAGAAA[-/AG]AAAATCTCCCAGGAG	78514
rs244101276	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77265583	TTATGGCCAAAGAAG[A/T]ACCCATCAGGGGCTG	78514
rs244105232	snp	C/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77254012	AACCAACCAATACAT[C/G/T]GGACCACATGGGGAC	78514
rs244110319	in-del	-/TAT			intron-variant	Arhgap10	Mm_Celera	8:77330840	GTGAACATATACAGA[-/TAT]ACTGTTCTCATTTAC	78514
rs244113545	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77498750	GAAGGAGAAAAGCCA[G/T]CTCCCCTTATCTCAC	78514
rs244124069	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77464933	ATAAATAAATAGATC[-/T]TTTTTTTAAAAAAAG	78514
rs244173637	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77442478	ATGAGATAGTCAACC[C/G]AGCTGGTTCCAATAA	78514
rs244180837	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77375373	TCCCCTTCTGTGAAT[G/T]TTCTGGGAGCCCAAG	78514
rs244196080	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77418339	AGATGCTGGGTTCCT[A/G]TGTCATTCCAGAGCC	78514
rs244202055	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77483448	AAAGAGGTTAAGGCT[A/G]GCCTAGGCTACAATT	78514
rs244215737	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77489536	ACACACACACAAGTG[A/G]CTGCTAAAAAGGCAT	78514
rs244221938	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77383988	TCATGTGCTGTGTGT[A/C]AAAAGCTCAGCACCT	78514
rs244231758	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77448428	ACATGCACACCATGA[A/G]ATTCCAAGTATGCTA	78514
rs244241233	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77395951	CTTCCTACAGACATA[A/G]CCAGACATTTCTTAG	78514
rs244248128	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77407082	TTTAGCTCTAGTTTC[A/G]GGGGACCTGACGCCC	78514
rs244251181	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77491238	CCCCTTCTGGTGTGT[C/T]TGAAGACAGCTACAG	78514
rs244254837	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77266318	TGCCTGAGTCAGGCT[C/T]TCTCAGAAAAAGAAG	78514
rs244255588	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77260020	ATTTAGGAGCACAGA[G/T]TACACACCATGACAT	78514
rs244278135	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77488835	GTAAGATGGGTAGCA[G/T]AGCAGTGGTATGGAC	78514
rs244279834	in-del	-/CAT			intron-variant	Arhgap10	Mm_Celera	8:77441330	TTCTCCCTCTCCCTG[-/CAT]CAGGGACAGGACTAG	78514
rs244284103	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77345320	CATGTATTTGATCAA[G/T]ATTAAACAGACAAGT	78514
rs244287085	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77491097	AAAGAAGAAATAAAA[A/C]TAAAAACTAAGGGGC	78514
rs244298796	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77459378	GGAGAGAAAAATCAA[A/G]GACAGAACAAACTGG	78514
rs244300098	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77378538	TGTGCTGTGCTACTT[C/T]ACCATAGGTCCAAAG	78514
rs244303014	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77371142	ACATTTATTTAATAG[A/G]AATGACTCATGGAAA	78514
rs244304895	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77319558	CACCGCCTGTGACAA[C/T]TTTACAATATGACAA	78514
rs244307390	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77307143	CAAACATGACCTCAG[A/T]GTAAAGGGCTGGAAA	78514
rs244309382	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77498022	CCTACAGGAGTGGTG[C/T]CACTCCACAGACTGG	78514
rs244309978	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77440190	GCACTCAATAAGGCA[A/G]CAAACTCAAAAGGGG	78514
rs244311178	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77447062	GTTTGGTTTAAGGGG[G/T]GGAGGGTTTGAGTGG	78514
rs244342908	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77350100	GCAAAGCCCACATTT[C/T]GGGCTTCATTACCTC	78514
rs244343245	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77423864	GGTGTGCAATGCATG[A/G]CACAAAGAGTCCTGG	78514
rs244344141	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77308840	TATGGTTCCTTGGCA[A/G]AGCATTTGCCTGGCA	78514
rs244367791	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77497283	ATGGTGCTTAGACCT[C/G]AACGTGGGTCCTCTG	78514
rs244371852	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77446750	GTGGGTTTTGTTAAA[A/G]TGGCAACTTCCTGAG	78514
rs244372624	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77467037	TGTCATCATCCCCAC[A/T]CAGCGGGACTCAGCA	78514
rs244400224	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77406930	CAACAACAACAACAA[C/T]ACAAAACACGTACAT	78514
rs244401891	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77350947	ACGATTAAGCAGCAT[A/G]CACTAGGGATAAAAG	78514
rs244413431	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77509792	TTCCCTACAGAAGAC[C/T]GCAGTCACACACACA	78514
rs244413432	snp	A/G			upstream-variant-2KB, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77518550	CCCTGCTTGTGTTCT[A/G]TTCTGGAGATTAAAT	78514
rs244425434	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77410216	TTTTCTATGTACATC[C/T]ATTGCTACTAAGGCC	78514
rs244435034	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77360318	CTGTCCAATTGGAAC[C/T]ACCACCCCAGCTGTG	78514
rs244443269	in-del	-/AAA			intron-variant	Arhgap10	Mm_Celera	8:77309941	TTGAAGCAAGAAGAC[-/AAA]AAAAAAAACAAGCAA	78514
rs244449480	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77472615	CAAATATAATCTATT[A/C]ATATATTACTATAGA	78514
rs244459287	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77343142	GAAACAGTCAACACC[C/T]AAGAAAACACGCTAC	78514
rs244461684	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77351910	AATTCTTACCAGGTC[A/G]ATGCACATCAGGTTG	78514
rs244462465	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77316111	TGCCACCCATCAGTA[G/T]AAGATCCTTCCTCCT	78514
rs244465180	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77413957	GGTGTTCGAAACGAA[C/T]GACCTGACCCAAGCT	78514
rs244467393	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77365264	TCGCAACAGCAGCAT[G/T]CCTGCAGACTATAAA	78514
rs244468678	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77271480	GTGAGGCATGGGAGG[A/G]ACTCTGGAGGGTATG	78514
rs244475206	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77447251	AAAGGCATGCAGGAC[C/T]CTGCAGACACAATCC	78514
rs244478406	in-del	-/TTT			intron-variant	Arhgap10	Mm_Celera	8:77347401	TTGTTGTTGTTGTTG[-/TTT]TTGTTGTTGTTGTTT	78514
rs244489585	snp	A/T			intron-variant, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77517543	CCCGGTCTTAGGAGC[A/T]CTGAGCCATCCCACT	78514
rs244507282	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77324122	TCTTAAGAAGAATGG[A/G]GAAGCTGCCCATCTT	78514
rs244508675	snp	A/C			upstream-variant-2KB, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77518242	CGAAGTGGACGCCTG[A/C]CCGAACGGGATGGTG	78514
rs244508703	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77353877	ATTATTCTAAGTATT[C/G]TAAGTCAAAATAAGT	78514
rs244509558	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77330631	GCCGCAATGCCTCCT[C/T]GCTGAGTTACTGCTG	78514
rs244535559	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77308484	AAATAGAAACAGAAG[A/G]AACACTAGCCAATTC	78514
rs244551869	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77406565	ACAGGGGACAGCAGG[C/T]CTGCCCGCAGAGAAT	78514
rs244557281	in-del	-/CCG			intron-variant	Arhgap10	Mm_Celera	8:77323985	AAAAAGACTCCCTCC[-/CCG]ACCCCCCCCATCCCC	78514
rs244559581	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77324585	TTCAGTCTCTGGTGG[C/T]TAGTAAGATACTAGA	78514
rs244568770	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77265521	AGGTAGGAGTATTTT[C/T]TGCATCTGTTAGGAA	78514
rs244572873	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77265922	CATGCTGCAAGACAA[C/G]CCCAGAGAGGTGGCA	78514
rs244591267	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77338350	GCTACCTAAAAGGTT[A/G]TTACTTGGTATCATT	78514
rs244599324	in-del	-/GGCAGGCGGGCG			intron-variant	Arhgap10	Mm_Celera	8:77416630	CAAGACAGACAGACT[-/GGCAGGCGGGCG]GGCAGGCGGACGGAC	78514
rs244609484	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77325070	TCCAACTGAGAAGGA[C/T]GCAGGCATGTGGACA	78514
rs244611610	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77428305	AATTACTAAACCAAG[C/T]GAAGATTAAATATTA	78514
rs244613372	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77440627	AAAACACCATTGCAT[A/G]TGAAATAAAAAACAC	78514
rs244618456	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77435891	ACTAGGGCAGGCTTA[C/T]AGTTTCAGAGGTTCA	78514
rs244626639	snp	C/G/T			intron-variant	Arhgap10	Mm_Celera	8:77253367	CTGGAATGGTGTGAA[C/G/T]TGCTCCCCTCTCCAG	78514
rs244632144	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77471419	CAACCCTATAGGTGG[A/G]ACAACAATATGAACT	78514
rs244642169	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77376872	TATCTTCTGGGAAAA[C/T]TCGTCCTGGGCCCCC	78514
rs244659879	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77477247	AGACCTCTCCATTCA[C/T]AAATAACACACCTTT	78514
rs244660233	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77512277	TGCTCGGAGATTCTC[A/T]TTCAGAACCAAAGAC	78514
rs244665647	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77404078	ATTGAAGGAGGGGGG[-/AA]AAAAAAAGACAGCAC	78514
rs244669777	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77296042	CTTGTTGGAGTAGGT[A/G]TGTCACTGTGGGTGT	78514
rs244669864	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77398089	GGTAAATGGTTACAA[-/G]GCCCAATGGTGGAAG	78514
rs244670935	snp	A/C			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77516050	ACAATGGCTCAAAAG[A/C]ACACACACAGTTTTT	78514
rs244697430	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77376351	ATTTACCCTTATTAG[G/T]TTAGTTCAGTCCTTT	78514
rs244700854	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77276983	CACCCGTCCCCTTCC[A/G]GCCAGGAAACAGAAA	78514
rs244703408	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77447796	GCTAGCTTATCATTC[A/G]GAGGTTTAGTTCATC	78514
rs244719807	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77476893	GCCTCTGCCTGCTAA[A/G]TGACGTGGGTACCAG	78514
rs244743505	in-del	-/TTTGTTTG			intron-variant	Arhgap10	Mm_Celera	8:77514703	ACAGTTTAATTGGTT[-/TTTGTTTG]TTTGTTTGTTTGTTT	78514
rs244750957	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77377245	AAAAAAAAAAGAATT[A/G]CTGATTTTGCATTAT	78514
rs244753016	in-del	-/TGTCTGTC			intron-variant	Arhgap10	Mm_Celera	8:77255590	GTGTGTGTGTGTGTG[-/TGTCTGTC]TGTCTGTCTGTCTAC	78514
rs244778164	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77289492	AAGGCGTTTGACCCA[A/G]GTGCTCAAGGAGCCG	78514
rs244790573	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77330030	GCTTCACTGCTGTCC[C/G]CTCTCCGTCTGTGTT	78514
rs244796271	snp	C/G			intron-variant, downstream-variant-500B	Arhgap10	Mm_Celera	8:77358174	CTCTCTCTCCACTAC[C/G]CCCTAGTCCCCCCAT	78514
rs244799614	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77283855	GGGTCAGCCAAGGTG[G/T]AGCACAGGCTGTAGC	78514
rs244800326	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77485875	GGGGTTCTCAACCTA[C/T]GGTCATCTGCCCTCT	78514
rs244804252	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77465143	ACAACACCAGACACG[G/T]TCTACACCATCCAAA	78514
rs244812481	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77271816	CTTTATTGGGGGATG[C/G]GGGAGAATGACTTTG	78514
rs244821225	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77408078	CTAGCCTTTATCATT[-/A]AAAAAAAATTAATCC	78514
rs244827897	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77454474	ATTTCCTGAGTACAG[C/T]GACAGCTTGTCGCCT	78514
rs244831820	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77314716	ATGTAGTGAGGCAGA[C/T]GCTTCTGCCATAGGA	78514
rs244839854	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77434384	CCCCTCGACCAGGTT[C/G]TTATCTGACCTCTAA	78514
rs244849746	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77403303	CACGAGACAGCACTA[A/T]GGTAAGCATCCCTAC	78514
rs244853800	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77352141	CAGACCAGTGGTCCC[A/C]AACCCCTTTGGGGCT	78514
rs244860537	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77419826	CACAACAACTCAGAG[C/T]TAACATAACCAAGTT	78514
rs244861457	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77483334	GGAGGCGGAGGGGGA[-/G]GGGGGAGGGGAGGGG	78514
rs244862710	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77471597	CCCGCAGCAGCCAGT[A/G]CTCTTAACCAGTGCT	78514
rs244862819	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77464755	TTCAAAAATGCCTTA[C/T]CTAGGGCTGGAGAGC	78514
rs244867782	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77258105	AGCCCATGGTGGACT[A/G]GTAGTCTTGGGTTCT	78514
rs244883409	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77497676	TTCCCCTGAAAGGGC[A/G]GAGGTCCACTACACT	78514
rs244885090	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77299859	TTTAATCCCAGCACT[C/G]GGGAGGCAGAGGCAG	78514
rs244903401	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77252938	ACAACCACTGCTCAG[C/T]TGTTCTGGAGATGGC	78514
rs244904142	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77346990	GAGGCAGGGGTCCCT[-/A]CAGAATGGTGCTGGG	78514
rs244912388	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77397984	CCACTGTCTTCCATG[C/T]CGCAAAGGACAGTCA	78514
rs244912959	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77470928	GGAACTGAGCCCAGG[G/T]CCTCTGGAAAAGCAG	78514
rs244913430	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77441032	AAAAAAAAAGGCTAC[A/G]AAAGCCAAGGTCTAC	78514
rs244918658	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77253229	TCCCTTTTCCTAGGG[A/C]CCCCGTTCTCTACAG	78514
rs244929850	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77419119	ATGCAAATATAGAGC[C/T]GTGAGTTTGAATTCC	78514
rs244931632	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77505848	TCTCCGAGCAGTCAT[A/G]ATCTACTCATTATTG	78514
rs244957794	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77295288	TTCTCCTTCTGAGGA[A/C]ATAAAAACAAGAGAC	78514
rs244959399	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77420760	GGCCTGTGTTAAAAC[A/G]AGCACTGTGAGTTGA	78514
rs244966091	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77331236	TTGACTTTTTTTTTT[C/T]CTTGGGAAAAAGGAA	78514
rs244971307	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77371517	CCCAGTTCCCGTGTA[A/C]AACAAAGCATTACCG	78514
rs244976983	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77398410	GATGTCAGATGTCAT[C/T]GGGTGCCTCCAGTGA	78514
rs244984772	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77425212	AAAAGTAAAAGAGAT[A/C]TTTTAAAAGCCTATT	78514
rs244988493	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77505543	CGTAGGAGGCAGAGA[A/C]AGGTGAATCTCTGTG	78514
rs244991488	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77512972	TATGTAGCAGAGAAT[A/G]GCCAAGAACTTTTGA	78514
rs245019070	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77427037	TTTGGCCATGTTTTT[G/T]ATCCTAACAACCCTA	78514
rs245048577	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77415586	GCCTTTGCACCAGAA[C/T]AAGCAGGGTTATTTG	78514
rs245053444	in-del	-/CC			intron-variant	Arhgap10	Mm_Celera	8:77496533	CATGATGCTTTTTTT[-/CC]CCCCAAATGTGCCTG	78514
rs245058105	in-del	-/AACTTAACTTCCTCTTCCGT			intron-variant	Arhgap10	Mm_Celera	8:77454349	CCTACCAAGTGTGAC[-/AACTTAACTTCCTCTTCCGT]AAGTTGAATGTCTTG	78514
rs245058366	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77256939	AGCACAGGGATGGTG[C/G]CAGAGAGGGAAGTCA	78514
rs245060314	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77382636	AGCTCCTGGTGTAGC[A/G]CGTAGCCGAGGGCTG	78514
rs245067284	in-del	-/TTTGATCTATACA			intron-variant	Arhgap10	Mm_Celera	8:77336192	TCTGAGAAAGAGCTG[-/TTTGATCTATACA]TTCATGTACCCTTTT	78514
rs245068859	snp	A/G			synonymous-codon	Arhgap10	Mm_Celera	8:77426390	CTTGTCGATGAGACT[A/G]TAATTCTTTTCCGTC	78514
rs245074013	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77373839	CTCCCTACTTCTGTG[A/T]CAGCCACTTCCTCAG	78514
rs245075627	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77325788	ACAGAAGAATGCCCA[C/T]CACATGCAACCCTTA	78514
rs245077750	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77459195	ATTTTCGTTAAAGTT[C/G]TCATTTGACTCTCTC	78514
rs245083359	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77272810	ATAGTTGGTACTGCA[A/C]ATCTGGTATGTAGAA	78514
rs245093139	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77400064	TCCTTAAGATCAAGG[A/G]ATTGAAGTCTCCAAA	78514
rs245112872	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77273150	CACCAAATAAATGTA[A/C]ATGTAAACAAAAGGA	78514
rs245117987	in-del	-/CACAGGCTGCTCC			intron-variant	Arhgap10	Mm_Celera	8:77313700	AAAACAGAGTGGCCA[-/CACAGGCTGCTCC]CACAGGCGGGTGGTC	78514
rs245121438	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77447434	CATTTCAATCTCTTC[A/C]TCTCATCAGTTCACT	78514
rs245125193	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77501960	AAGAGGACTTGGTGG[G/T]CTCCCAGGCCCTCCT	78514
rs245125799	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77467264	GGAAAAGCAAACATA[C/T]GAATAGTCTATATAT	78514
rs245126954	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77296984	ATGCACTCTCAAAGC[A/T]CTGAAATCGCAATTA	78514
rs245148835	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77410114	AAACCCCAATTTACT[A/G]TAACAGCAAACTCAG	78514
rs245161465	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77297402	TACCTCCAGTTCCAC[A/G]GGATCCAATGCTCTC	78514
rs245172493	in-del	-/GAG			intron-variant	Arhgap10	Mm_Celera	8:77509484	GAGGAGGGGCTGGAA[-/GAG]GAGAAGGAAGGAGAG	78514
rs245176523	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77452813	CCTGTTCTTCCAAGG[A/G]ACAAGGGTTCACTTC	78514
rs245181133	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77388097	ATCAGTGCTGGGACC[A/G]AGTGCCAACCGTCAG	78514
rs245193338	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77466353	GGGAGATACAGAAGA[A/C]TCTTGATGGGAAATA	78514
rs245198862	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77300125	aagaaagaagaagaa[A/G]aaagatgaagaagaa	78514
rs245202298	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77267810	AAACATCAAAGGCTT[A/G]AGGAGGAGGCTAGGC	78514
rs245206516	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77336417	ATCCAAAACTATTTC[A/G]AATCTGTTATTTAAG	78514
rs245209162	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77507651	GATCCAGACTCCGAT[C/T]AGGAAGCTCGATGTG	78514
rs245221221	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77372453	ACTTGCTTAACAATC[G/T]CCTGAGTTGTTTGGA	78514
rs245223247	in-del	-/T			intron-variant	Arhgap10	GRCm38.p3	8:77404795	TTTTTTTTGGTTTTC[-/T]GAGACAGGGATTCTC	78514
rs245224711	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77405555	TCTTAACCGCTGAGC[C/T]ACCTCTCCAGCCCCA	78514
rs245230181	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77452489	TAACAACTCTGTTAT[C/T]CATTTTGCAAACGTT	78514
rs245234074	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77343771	GAGGAATGTAAGTGC[G/T]GAGCAATGGGCACTG	78514
rs245239203	snp	A/C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485511	ACTCCTCTCCACTCC[A/C/T]GTCCTTCAAAACCAG	78514
rs245249458	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77291014	CCCAACAGATGTATT[G/T]CATGTATTAGAGCAC	78514
rs245250454	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77358721	CTCAAGAAAAGTATT[A/G]TATGCAATCTTTTAA	78514
rs245257493	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77421276	TGGACTCTTAGGCTC[C/T]CAGATGAAAGGCAAT	78514
rs245259538	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77500783	CACGGAGCCCTCGCT[C/G]TAGCTCCAGATACCA	78514
rs245310900	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77404148	GGCCTCCACCCAGCC[C/T]CCTGCTGCTCACAGT	78514
rs245310956	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77408986	CCAAAGCAGGGTCAG[C/T]AGGCGCCTGACACGC	78514
rs245312726	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77421827	AGAGTCATGCCCTCA[C/T]GTGTCCTCGGTATGA	78514
rs245313297	in-del	-/CTGACCT			intron-variant	Arhgap10	Mm_Celera	8:77419213	GTGGGACGGGTGAGA[-/CTGACCT]CTGGAGCTCTCTAAC	78514
rs245318021	snp	A/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494184	CCCAGTGAGCCCAGG[A/T]GACATGTGGCCTGAG	78514
rs245321691	in-del	-/AAGGGACGTT			intron-variant	Arhgap10	Mm_Celera	8:77278055	CCGAGTGCGTAAGAA[-/AAGGGACGTT]AAGGGACGTAAGCGG	78514
rs245326779	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77420473	CGGTATGGCGGGGGG[C/G]CTGTGCCCCTCACTG	78514
rs245343525	in-del	-/AAG			intron-variant	Arhgap10	GRCm38.p3	8:77254517	GGGGGAAGGGAAGGG[-/AAG]GAAAGGGGAAAGGGG	78514
rs245355089	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77370186	TACAGATAAAAGCTT[C/T]GATTCCTAGTGTTGG	78514
rs245357940	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77381520	GAGTATGGGGCCGCC[A/G]GACTGGCTTCAGTAG	78514
rs245366439	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77491779	CGGCCTAGGAGGCCA[A/G]GACCAGGGAGTCAAC	78514
rs245372750	in-del	-/CT			intron-variant	Arhgap10	Mm_Celera	8:77329189	ATTCAAGTTCCCTTC[-/CT]CATGCTACGCTGAGC	78514
rs245375038	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77311842	TAAAAAGCACTAAAG[C/T]TACTGCCTACTCATC	78514
rs245375044	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77428848	ACTTCTTACTAAGAC[-/T]TTAACATTTTCATAA	78514
rs245389518	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77373147	CTACCACTTAGCTAT[A/G]AGCCATCCTTCCTTT	78514
rs245404043	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77337105	ACGGACGGACAGACG[A/G]CCTTTGGGTTTTGTC	78514
rs245407017	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77312437	GCCAGGACATCCAAA[C/G]CACCCATAAACCATG	78514
rs245417569	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77283622	CAGTTGGTTTTGATT[A/G]GTAAATAAAGTTGCC	78514
rs245431647	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77499808	CTTTATGTCTAATAG[A/G]GTCCCTCACCAGATG	78514
rs245435873	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77276172	ACACACCAATGcata[C/T]acacacacacacaca	78514
rs245442911	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77363508	CACCGTTTAGACCTA[C/T]TGACCAGCAAGCCTG	78514
rs245460493	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77448192	ACACACACACACACA[A/C]ACATACTCCTTATAT	78514
rs245465277	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77452963	CATTTTTTAAAAAAG[C/T]GTTCCTTTGAATCTG	78514
rs245475289	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77380035	AGGAAAAAAAGCACT[A/G]TGCTATCTTCTTCAG	78514
rs245479447	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77331559	GAGAAATCTAGATGG[G/T]TCATTGTGATGCAGA	78514
rs245485425	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77496470	CTGTCCTCAGCTTAA[A/G]CCCCATTTCCTTCCT	78514
rs245486927	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77319512	TTGCTAAGAGAAAGG[A/G]GACACATTGACAGCA	78514
rs245487625	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77354044	CTGATTACAGTGCTG[C/G]TTTCATGGGAGAATA	78514
rs245493873	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77253800	AGCCTTCTGAGATTC[C/T]TACGATCAGAATACA	78514
rs245510878	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77264405	TTGACACACTTCCTG[C/T]AGCTTTTCCTATGGA	78514
rs245519692	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77275082	GGAGGGTGTGGGGGA[C/T]TTTTGGGATAGCATT	78514
rs245524549	in-del	-/ATCCGT			intron-variant	Arhgap10	Mm_Celera	8:77385143	GGGTAGAAGTTTACA[-/ATCCGT]ATGCGTCAGCAGGAT	78514
rs245533563	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77273257	AAGAAAGAAGGGTGC[A/C]TGGTGAGACTCTGCA	78514
rs245535799	snp	A/T			synonymous-codon	Arhgap10	Mm_Celera	8:77346331	CTCTGGCAGTTTGTG[A/T]ACCAAGAAGTGGATG	78514
rs245537656	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77280910	ACCTCTTACAAGATT[A/C]ATTTATAATTGAGAA	78514
rs245567576	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77356948	TATAACACCATGAGG[A/G]TAAAAAAGACCACAG	78514
rs245575057	in-del	-/AACAT			intron-variant	Arhgap10	Mm_Celera	8:77406667	TCTGAGAGAGACATC[-/AACAT]AATGGCTTTCTGAGG	78514
rs245587487	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77312791	CAGAATATGCACCTT[C/T]GAGTTGTTTTGCTTT	78514
rs245589143	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77499844	CTGTATTAAAGACTC[A/G]CAGCATTAGGAAGGC	78514
rs245602605	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77332952	TTAGAAATTATTTTT[A/T]AAAATGGATGTTATA	78514
rs245609986	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77386064	TCTGTTGTCTGTCAG[C/T]GGCTCGGCTCTTTAC	78514
rs245612856	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77472356	GCCATGGTGATTATG[C/G]CAAGTAAGATATATG	78514
rs245621250	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77342012	CATATTATTCCACAC[C/T]TCAGCCTCAAGCCTT	78514
rs245634922	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77460086	ATCTCAGAGTTCCAG[G/T]GCAGCCTGCTCTACA	78514
rs245663084	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77327277	AACCAGTCTAAGCAC[A/G]AACCGATAACTGTTA	78514
rs245677866	snp	A/C			downstream-variant-500B	Arhgap10	Mm_Celera	8:77250359	ATATTAGGCCGGACA[A/C]ACCAAATAGTAAATT	78514
rs245678220	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77289454	TGACATCTGTCCTCT[A/C]ATACACTCAGAGGAC	78514
rs245684666	in-del	-/AC/ACACAC/ACACACACACACACAC/ACACACACACGC/ACACACACACGCAC			intron-variant	Arhgap10	Mm_Celera	8:77284063	TAATTAGCTAGTACT[lengthTooLong]ACACACACACACACA	78514
rs245708298	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77443368	CAGTTAAAGAGTATA[C/T]GATCAGTCATGGAGG	78514
rs245711109	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77251053	TGTTCCCGGTGCTTA[A/C]CCCTGACACTCACCA	78514
rs245733965	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77478901	AAAATGAGATTTACC[G/T]CATTCTATCCCCACC	78514
rs245738663	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77281516	GAAGTTGCTCCATCT[C/G]ATGCATCCCTTCCGG	78514
rs245755367	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77375151	AACTCGGGTGCAAGC[-/G]ATGGAAAATTTCGAC	78514
rs245758196	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77387990	GAAAGAGCATCTGTG[A/G]TTCCTCCTCAAGTTG	78514
rs245764871	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77379414	CTCTGCCAACTTGGT[C/T]CCCTTACTTAGGGAG	78514
rs245767776	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77305478	ACTGTGTTATAAAAA[A/C]TGATTTAGAAGAAAA	78514
rs245770148	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77450424	TTTAGGGTAACATAC[A/G]TGCAAGTCAAAGGCT	78514
rs245776341	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77515563	CTTGCCAAAATGGTG[C/T]ACACCAACCCTTTTA	78514
rs245788899	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77273742	TACCTACTGCACACA[A/T]TAATGACAGGCAACC	78514
rs245791424	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77434279	ACAATCTCCATAAAT[G/T]AAGATACTTGGGCCA	78514
rs245801609	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77292039	TTAAATAACTATGGT[A/T]CCTATTATGAACCAA	78514
rs245804512	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77280141	AGGGAAACAGCTGTG[A/G]TGAGAAGCAGGTTTG	78514
rs245808305	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77362346	TTAAGACATTTGAAA[A/G]AGAAATGGTAAAACT	78514
rs245834425	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77262909	TTGGAGAATAGGAAA[C/T]GTTGATGAGAGGAGA	78514
rs245843778	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77414358	TGATACCAAATAGCT[A/G]CTGCTGTGAAATTGC	78514
rs245861706	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77318291	CAACCAATACACTCT[A/T]TGTGGCTACATAATG	78514
rs245871055	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77364976	ACCCACCCAAGTAAG[C/T]GGTACAAGAGAAGAT	78514
rs245871994	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77361361	GGGAGTCAGTGCCCT[A/C]GCCACCACAGACGTG	78514
rs245877610	in-del	-/GACAAACA			intron-variant	Arhgap10	Mm_Celera	8:77511575	GGCTTCATGTGGATG[-/GACAAACA]GGCTACACTGCTCAT	78514
rs245891688	in-del	-/AG			intron-variant	Arhgap10	Mm_Celera	8:77386235	CGGGTTATTAAAAAA[-/AG]GGATTAAAGGATTAG	78514
rs245899538	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77489334	TGCACTTGAGGCATG[A/C]GAGTGCATGTGTGAG	78514
rs245900162	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77318179	TTTAGTACAACAATA[A/G]GAAAAGCAACTAAAT	78514
rs245903677	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77332259	TCGGGGTGGCCCACC[A/G]TGTTCATGCTGCTTG	78514
rs245904010	in-del	-/CAA			intron-variant	Arhgap10	Mm_Celera	8:77324977	CCACAGAGGTCAGGC[-/CAA]CAATGCACTGTAATG	78514
rs245918086	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77483422	ATTATTAAATTAAAT[G/T]AAAAATTTCAAAAGA	78514
rs245918305	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77278781	TGGAACGTAAGTCTT[-/G]AAAAGTGAATGACGA	78514
rs245928304	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77409215	CATTTCCACGCTGCT[A/G]TGGCGAGCACTGTCT	78514
rs245931790	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77361680	CAGGTTTCCCCTGCT[A/C]TGCCCAGGTTTTGTT	78514
rs245933850	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77474078	TTATGGAATAGCAAC[A/G]GCCCAGCCAGTGACT	78514
rs245941057	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77432458	TAATACAGAGAATTA[C/T]GCACATGGCTGCAGC	78514
rs245947820	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77405167	AGCCCCAGCTCGTGG[A/G]ATTCATAATCTAACA	78514
rs245949477	in-del	-/TT			intron-variant	Arhgap10	Mm_Celera	8:77368825	ACAGAACTCTGCCTG[-/TT]TTTTTTTTTTTTTTG	78514
rs245950440	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77262958	AGCTGCAAAGCTATC[C/T]GCTCAGAAAGAGTGA	78514
rs245956397	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77363151	TGTTTAAGCAATGCT[A/T]ATTTGTATGTGTGTG	78514
rs245956832	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77422369	AAACTCTCCATCCAT[A/G]GGAGTTTTATAACAA	78514
rs245967713	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77254542	AAGGGGAAAGTGTAC[C/G]CCTGGCACACTAACG	78514
rs245971629	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77474649	TCCAAGACAGTACAG[A/G]TGGACATGGAGACTG	78514
rs245977684	in-del	-/AAAA			intron-variant	Arhgap10	Mm_Celera	8:77413636	CCGTGTCTGAAAAAG[-/AAAA]AAAAAAAAATACAGA	78514
rs245980925	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77473373	CCAAAAAGATACCCA[A/T]ATCAGTACTGTCTGT	78514
rs245987159	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77355220	GCCAAAGGCTGAGAG[A/G]AGAGAAATGGGGTGG	78514
rs245992402	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77341887	CCTGTTAACTTCTCA[-/G]GGAAAAAAAATAAAA	78514
rs246004276	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77496791	TCTCTCTATTTTACA[-/C]AGCTCTGGCTGTCTT	78514
rs246009323	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77400297	AAGGAACCCTAGGAG[A/G]CACCGTCTAGTTTCA	78514
rs246018818	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77428603	AACAGAACCCCACCC[A/G]TGTCAAAATCAATTC	78514
rs246019284	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77421799	TCATGAGGCATCACT[A/G]CCTGCAGAGCGGAGA	78514
rs246024516	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77334796	CAGGCAGCAAACCTC[A/G]GAGACAATTACAAGA	78514
rs246035854	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77413036	TTACTATGTGTCTAG[A/G]TGTGTCTATGTGAGT	78514
rs246037147	in-del	-/TG			intron-variant	Arhgap10	Mm_Celera	8:77369091	ATACTAGTCAATTTT[-/TG]TTTGTTTGTTTTGTT	78514
rs246054189	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77298380	ATTTTATGAACAAAA[A/C]TTATCTCAAATAAAT	78514
rs246063225	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77279757	AAGAGGGGCTCCTAC[A/C]ACCTGGTGTTTCATG	78514
rs246071295	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77400777	GGGTGTGTTTTCCCT[C/T]TTTGTACACATCTCT	78514
rs246075452	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77398703	AGCTTTCCCAAAACC[A/T]AGTATAAATTCATCT	78514
rs246077883	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77428069	GTTTCTTATGAAGCA[C/G]ACATATAAAATCTAG	78514
rs246084422	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77448786	ATCCCTGGCCCTGTG[C/T]ACACTGCCACATCCC	78514
rs246086523	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77429378	CCTCTCTAAAGAGAC[A/G]AACACTCAGCTCTTC	78514
rs246092757	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77334205	AGTCTGTAGAAGAAA[A/G]AACCCATGTTTGAAA	78514
rs246093216	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77430644	AGTCAAGGCAGGTAC[A/G]TCAAGACAGAGCACA	78514
rs246098943	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77287182	AGAAAAACAGTCTCT[-/AA]AAGATCACAGTAGAA	78514
rs246100045	in-del	-/GGGTATAAGCAA			intron-variant	Arhgap10	Mm_Celera	8:77348404	TAACAACAGAGGCTG[-/GGGTATAAGCAA]GTTTACTAGAGCTTA	78514
rs246123906	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77473192	CTGAGGAGTGACCCC[C/T]GACGCCCACTTCACA	78514
rs246135563	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77380529	TCACTTTCTGATCTA[G/T]AAGGTTTTTATCTAA	78514
rs246141320	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77436515	GGGACAGAAAGGATG[C/T]CCTATGGCAACGTTA	78514
rs246142461	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77428764	CAGTTAGTGGGGTAA[A/T]CAGCAACTGAGGAGG	78514
rs246168532	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77375611	GTAAGCTGTCATGAG[A/G]AGAAAGAAATATTCA	78514
rs246169091	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77438216	AGTTCACTGTTTCCA[C/T]GTGTAGTCTCTCTCT	78514
rs246173311	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77274728	CCAGGAGAGTGGGCA[C/T]TAAAAAATGTTTCTT	78514
rs246177973	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77335874	CATTTTCCTCTGCAC[A/G]AGTCCTACTCTGATG	78514
rs246202184	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77306916	CAGAAAAAGCAAGAA[A/T]GAAATTTTCTTTCAA	78514
rs246205933	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77270325	TATTATCCCGTTAAG[A/C]ATAAAAAAGGGCAGA	78514
rs246206145	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77275376	CTCACTGGACGATTA[C/T]GCCTAGCTGCCTGGC	78514
rs246211653	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77335984	CTCTCTCTCTTTCTC[A/T]cacacacacacacac	78514
rs246213599	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77469822	GGTTCAGGCTACCGA[A/G]GTTGAATATGATTCC	78514
rs246214587	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77281391	AGAGACTTGGGGAAA[C/T]GCGATGGGCCCTCTG	78514
rs246216363	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77418616	TGAAAGTCTTCATTG[-/T]TTTTAATGTGGGGTT	78514
rs246233370	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77308626	TTTCCTACTTTTATC[A/G]TGTTTAATTTTCCAA	78514
rs246233706	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77450799	GGGCAAGGCAGAGGG[A/G]AGCAAAGCGGACCCC	78514
rs246239403	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77455343	GATCAAGAAATGAGC[C/T]GGAGACACGGCCACA	78514
rs246262041	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77374191	CCTCATTTAAATCAC[C/T]ATCACCCCCTGTATA	78514
rs246269500	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77254421	TAATGGGATCTGATA[A/C]CTTCTTCTGGTGTTC	78514
rs246273686	in-del	-/AC			intron-variant	Arhgap10	Mm_Celera	8:77357780	AATAGTGAAATTAAA[-/AC]AGTCTTCCCTTTAGT	78514
rs246275882	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77475418	TGATCAACGGTGGGG[A/G]AAAACCGGCATTTAA	78514
rs246275915	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77469460	TCACGACCACAGCCC[G/T]GGGGACTGTATTAAA	78514
rs246281710	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77338732	AAACTTCCAGAAAGG[A/G]AACAGAAATTGACAT	78514
rs246287497	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77270821	GTGGGTAGTAAATGC[A/G]GAGTGGATCTGGCAA	78514
rs246294097	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77454907	AGCACAACAGCCACA[A/G]CGTGCCCTTGATGAC	78514
rs246306455	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77456131	TGCCAACAAGGGAAG[C/T]ACACATTCAACCCAG	78514
rs246308857	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77439661	TTAGGCTGCATGTGT[A/T]CTTGCATGCACACAT	78514
rs246323688	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77499713	GGCCATCAGAAAACT[C/T]GTATTTACATCACAA	78514
rs246336257	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77252025	CCCGTTGCGAGAAGT[C/T]CTGTGAATTCTGCTC	78514
rs246338225	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77339325	ACCATTCCATCACAC[C/T]GAGAAGTCAAAATAA	78514
rs246344406	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77350890	TGTCTCAGCCTCGAT[G/T]TCCTACCTCTTAATT	78514
rs246345632	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77368892	ACAATTAATTCCTTC[C/T]AATTTGTTGTTTCAT	78514
rs246350240	in-del	-/CGCT			intron-variant	Arhgap10	Mm_Celera	8:77314368	ACATCTTTCTCGAAG[-/CGCT]CGCTGCACACTTTCC	78514
rs246351738	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77480506	GACCAGGCTGGCCTC[A/G]AACTCAGAAATCCAC	78514
rs246365945	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77380777	GACTCCGCCGAGCAA[A/G]CATTCAATCTTTCAC	78514
rs246372541	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77384419	GCGTAGGACCATGAG[C/T]AAGAGCAACCTGCTA	78514
rs246373486	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77252374	GCTTTCATGGTGACC[C/T]AGCAGGCAACTGGAT	78514
rs246379335	in-del	-/CC			intron-variant	Arhgap10	Mm_Celera	8:77292751	AAGGTGTTAGATACT[-/CC]CCCCCCCCTTTGTTC	78514
rs246381415	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77405959	ACAAAAAAGCAGGAA[A/C]TCTGAAAATGACTTG	78514
rs246382732	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77410762	TTCTATGTGAACAGG[A/G]GTGGTCAACGAGTCA	78514
rs246383843	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77496099	TATCTCTGCCCCCTT[C/T]CCATGGTGCGCAGCT	78514
rs246384422	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77311342	GCCTGCGCTATGCAA[G/T]TACCTGTCTCGGTTC	78514
rs246385852	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77323916	TCCTGGGAAGTCAAC[C/T]AGGAATCTCCAAAGC	78514
rs246389835	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77497220	CCAGAAGAAAGAAGT[A/G]GGCACCAGATGCCCT	78514
rs246394179	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77505347	ACTCTTATCGATGGA[A/G]ATAAGACATGCTCCC	78514
rs246399175	snp	A/C/G			intron-variant	Arhgap10	GRCm38.p3	8:77446396	CGTGCATCACAAGAA[A/C/G]TAATCACTACCAAGG	78514
rs246406985	in-del	-/AGAGAA			intron-variant	Arhgap10	Mm_Celera	8:77274251	GAGAGGGAGAAGGAG[-/AGAGAA]AGAGAGAGCTTTCAT	78514
rs246407985	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77268645	GACATGTTATGGCCC[C/G]CAAGGTCTCTGTGTA	78514
rs246417432	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77340558	GGTTCTGCTGGGTAA[A/G]GCTTTTCACCCTGGA	78514
rs246418438	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77339421	TGTTATATGGCACCA[-/T]TCTTTGCAGCATTAA	78514
rs246420592	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77255268	CACAGTCTTGGGGAA[A/G]GGACTGAGGAACTAT	78514
rs246423631	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77381247	CAGAGACCATGGAGG[A/G]ACATAGTTCACTAGA	78514
rs246434322	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77486258	TGGGTGCATCAGGCT[A/G]TCCTTGAACTCAAGT	78514
rs246437096	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77315276	TGGCTTGCTCTTGGT[C/T]TATCCTTCCTGTACA	78514
rs246443507	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77406414	TGTGTGTTACTAAAT[G/T]TATCCCTAACACTAT	78514
rs246444020	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77495357	TCTCTTTCTTTCTTT[C/T]TTTCCTTTGTCAATT	78514
rs246445432	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77496813	GGCTGTCTTAGAGCA[C/T]GCTCTGTAAACCAAG	78514
rs246449197	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77502810	GAGACTTGCTCCCAC[A/G]GCCCAGCAGCCAGTG	78514
rs246452717	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77397831	AGTGAAGGGCTGCCT[C/T]TGGAACCGAAACGTT	78514
rs246467189	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77455089	ATGACTAAATACCCC[A/G]TTACAGTTTCTGTTG	78514
rs246471651	in-del	-/GGCCTA			intron-variant	Arhgap10	Mm_Celera	8:77323093	CTAGTGTCCCAAAAT[-/GGCCTA]GACACTTAACTCATG	78514
rs246476664	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77411862	TACGGATTAAACAGT[A/G]GGCGCACACCATCCT	78514
rs246482387	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77438036	GCATAAACTTTCCCC[A/G]GCTAAACCAATTCAT	78514
rs246483857	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77498444	ACACAGAAATACAAA[A/G]CACATCAAGAACTCA	78514
rs246491668	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77347523	CTGCCTCCCAAGTGC[C/T]GGGATTAAAGGCGTG	78514
rs246494679	in-del	-/TAAATAAATAAG			intron-variant	Arhgap10	Mm_Celera	8:77320281	AAATAAATAAATAAA[-/TAAATAAATAAG]TAAGTAAAAGGGAGT	78514
rs246494844	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77367298	AGGCGAGGGGGAAAC[A/G]TGCAGAACAAACCAT	78514
rs246499728	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77375275	GCATCAGCCTTGCCT[C/T]GAAGCTGCCATCTGT	78514
rs246504468	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77451529	ATTTTCCATGGCAGG[C/T]CATGTATGGGAAATG	78514
rs246504767	snp	A/G			intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77502193	AGCACTCAGTTTCAC[A/G]GCCACTTTTGTTCTG	78514
rs246513771	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77460580	GGAGCAAAGGCACAG[A/G]TGCACCTGCAGTTGG	78514
rs246516656	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77383704	ATAAAGAGCAGAGAC[-/A]AAAAAAGGGGAAGAC	78514
rs246527695	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77263045	CTCCAGGCACGGCCC[-/A]ATGGTACAATTCACC	78514
rs246535690	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77504003	AACTGTTAAATGACT[A/G]TAAATGCTGCCCCAG	78514
rs246541503	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77294707	CTGCTTCTCTGTCTG[C/T]TTCCCCATCACACTC	78514
rs246547117	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77382225	TGTATGCACTCAGGA[A/G]GGACATATACACACA	78514
rs246552476	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77436174	AAATAAAATGACTAT[C/G]AAAGTTTCCGATGGT	78514
rs246554943	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77361175	CAAGGGAGGGGGCTT[C/G]CGTTTCTTCCCTGAC	78514
rs246561949	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77444499	ACACTACAAGAAAAA[A/G]TTATGCACCTCGAAA	78514
rs246563900	snp	A/T			utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250729	GCTAGATGAGAACTG[A/T]CTCCAGCAACGCCAG	78514
rs246570517	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77340529	CCAATGAGAGCCATA[G/T]AGATTAGACAGGAGG	78514
rs246571504	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77356251	GAAGACCCAGAATCC[C/T]TTCCCAGGACCCACA	78514
rs246578299	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77287724	AGGCAGGTGGATTTC[C/T]GAGTTCAAGACCAGC	78514
rs246581804	in-del	-/GG			intron-variant	Arhgap10	GRCm38.p3	8:77483270	CACACACACACACAC[-/GG]GAGGGGAAGGGGGAG	78514
rs246592855	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484962	CAGGCTCCAAGCTCC[A/G]GGAAATGCTAGGCCA	78514
rs246603517	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77284897	AAAGACGAGAAGACA[A/G]TGATTTAGAGATGCA	78514
rs246604671	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77316872	ATTTGAAAGTGCTTC[C/T]CCACACACAGCAGAT	78514
rs246608955	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77260991	AGTACTGGGTCACTA[A/G]CCACCTCTTTCACAC	78514
rs246636809	in-del	-/CAA			intron-variant	Arhgap10	Mm_Celera	8:77461943	TACATAACACATTTT[-/CAA]CAACCATTATAACCA	78514
rs246637558	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77356801	CAGTGGTGACAAGGC[A/G]ACATGAGACAACAGG	78514
rs246638411	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77318710	CAGTTGGGAACGCTC[-/A]TGTCCCTCCTGCAAT	78514
rs246643409	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77255534	CAGCTTCCAGAGAAA[A/G]TCAAAGGGCAAGGCA	78514
rs246685273	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77256253	ATAAGAATTCATTAC[A/T]ATTTCAGTGCTATAA	78514
rs246685907	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77322351	GTCATGTCACACCTC[A/G]ATGGCTGCAAGTGAC	78514
rs246689395	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77461895	CTGTCTAAAATTTGA[C/T]CCTAAACTTTGATTT	78514
rs246689782	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77410300	GTACATAGACAGAAA[C/T]CAGATTATTTCTGAA	78514
rs246691979	in-del	-/TTTTTTG			intron-variant	Arhgap10	Mm_Celera	8:77330903	TGCAACCATTTTTTT[-/TTTTTTG]AAGATTTGGTCTGGC	78514
rs246701190	in-del	-/A			intron-variant	Arhgap10	GRCm38.p3	8:77491840	CTCAGACATGCCCTC[-/A]CCCCCGGCCCCCGAC	78514
rs246709409	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77339248	ATGACCTCCTGTCTC[C/T]ACGAGAATCAATGAA	78514
rs246711760	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77505268	GATTCCCTAAAGTAA[C/T]GACTACAGACACTAT	78514
rs246724461	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77266836	GAAACAGGACTTCAA[A/G]AAAACATTGGTTTAC	78514
rs246751017	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77286198	AGGCTCCACTCAGAC[C/G]CCATCATGTAGCAAG	78514
rs246754858	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77335630	AGAGCTAGAAAAGAG[C/G]AAACCAAAACTTGCA	78514
rs246761301	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77474762	CAGATGTGAGTAAAA[A/G]GTGAGCAAGGACTGA	78514
rs246763551	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77257837	CCAGCCATGCCTTCT[C/T]TGTCTTTAGACCTTT	78514
rs246766937	in-del	-/CCT			intron-variant	Arhgap10	Mm_Celera	8:77370503	TGGCAGATTTCCCAG[-/CCT]GCTGAGGCAAGGAAC	78514
rs246767166	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77481999	CTACACACAGTGCTC[A/G]CTCGCTCCCAGAGCA	78514
rs246790870	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77388472	ATGAATAATGGCCCC[A/G]GTGTGCGTGTGCTGC	78514
rs246793342	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77278172	TGGTGCTGAGCGGGG[C/T]CCTGCAGTAACTGCA	78514
rs246803825	in-del	-/TTTT			intron-variant	Arhgap10	Mm_Celera	8:77368824	ACAGAACTCTGCCTG[-/TTTT]TTTTTTTTTTTTTTT	78514
rs246811986	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77330010	GGAAACCTATAAGCC[A/G]TTAAGCTTCACTGCT	78514
rs246818329	in-del	-/TGACATAAGC			intron-variant	Arhgap10	Mm_Celera	8:77461660	TTTGTAAGTGTGAAA[-/TGACATAAGC]TGTCATCTTTAAAGT	78514
rs246820810	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77481318	TAGTAGCAAATGGAG[A/T]CAGAAGGAAGATCAA	78514
rs246824895	in-del	-/GGGA			intron-variant	Arhgap10	Mm_Celera	8:77452206	GAACACCTCATGACT[-/GGGA]GAGAAAGAAGAAGGC	78514
rs246843842	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77388927	CCACCCCAATGATTC[A/G]CCTCCAGAATATTGC	78514
rs246846741	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77452773	TTTGAGGGCTGGAGA[C/G]ATCGCTTGGTGGTTA	78514
rs246848263	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77381908	TGATTCTTCCAAAGA[A/C]TGAGCTGAATTGTAT	78514
rs246850108	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77446574	AGGCTGTGTGTGGCG[A/G]CACACACTTGTGCCC	78514
rs246863456	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77403049	GGCTTTCCACGCCAC[C/T]TCATGCTTCAGGAAC	78514
rs246868747	in-del	-/AA			intron-variant	Arhgap10	GRCm38.p3	8:77451718	TGAACTTTATTTTTT[-/AA]TTAAAAAATGGGCAA	78514
rs246884552	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77284056	AGTAGCCTTAATTAG[A/C]TAGTACTACACACAC	78514
rs246900477	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77362515	CATTATCAGTAAAAT[A/G]TGCTCTGAAAAATTT	78514
rs246909242	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77272546	CCCCCAACCCTGAAC[-/T]TTTCCAGCCCAGGGG	78514
rs246912287	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77315529	AGATGAGCAAACTGA[C/G]GTCCCTGAGGCTCAA	78514
rs246922556	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77310714	CCACCGAGCAGAAAG[C/T]CCAATCAGCGCCTTA	78514
rs246924049	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77323437	TTTTATCAACTCCCG[C/T]GGCACCTACAGGAAT	78514
rs246928099	snp	G/T			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519828	AATGAATAATGTCTG[G/T]CTCCAAGCCAACCCA	78514
rs246946751	in-del	-/TTATTA			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503278	ATAACAAATTTACTT[-/TTATTA]TTATTATTATTATCC	78514
rs246953266	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77451133	ACCTCCTGCAGCTGA[-/T]CAGTGTGCATCTTTC	78514
rs246958487	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77259002	TCCTAAGAGGGATGT[C/T]ACAGCCCTTGCGTGT	78514
rs247005072	in-del	-/G			utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250710	CAATCAATGCCCAGT[-/G]CCTGCTAGATGAGAA	78514
rs247023995	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77264518	TCACTAAAAGACACA[A/T]GGAGATCTCAAACTC	78514
rs247025614	snp	C/T			intron-variant, missense	Arhgap10	Mm_Celera	8:77476566	GACAGAAGAAAACTG[C/T]TGGTCCATGGCTTCA	78514
rs247029630	in-del	-/CAGCACTTCACTGTTGGCGG			intron-variant	Arhgap10	Mm_Celera	8:77454213	GCAAACGCAGGCCCC[-/CAGCACTTCACTGTTGGCGG]CAGCGCTTCACTGTT	78514
rs247046798	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77422192	GAATTCCCACGAGAC[A/T]ACATTGTGTTAAGAA	78514
rs247054728	snp	A/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77257312	CCCAACACAGAGCTC[A/G/T]TGACAGTACTTACCA	78514
rs247059638	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77481661	TTCTTTCTCTTTAGC[-/T]TTCAACTCTCAGGAG	78514
rs247066887	in-del	-/G			intron-variant	Arhgap10	GRCm38.p3	8:77449445	CTTCTTACATGGGTT[-/G]GGGGAAGCCAAACTT	78514
rs247068635	in-del	-/CC			intron-variant	Arhgap10	GRCm38.p3	8:77471646	TCTCCAACTCCCCTT[-/CC]CCCCCCCCCCTTTTT	78514
rs247070530	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77372869	GCATCCGCCCTTCCA[C/T]CCGAGTCCTCCAGGG	78514
rs247071674	snp	G/T			intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77492413	GCACATGATAGGTTG[G/T]TTTTTTTTTTTACCT	78514
rs247072261	in-del	-/GTG			intron-variant	Arhgap10	Mm_Celera	8:77412281	ATGAGAACAGTCTGT[-/GTG]GGGGGTGTGTGTGTG	78514
rs247077041	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77475900	TAATCTTAAGTATAA[A/G]AGAAGACACTGGCCA	78514
rs247080621	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77464275	GGGAAGGGTTTTGAG[-/A]AGCAGCTGGGGTCTG	78514
rs247100333	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77346015	GATTCAACAAACCTA[A/C]AGGGCACATTCAGTC	78514
rs247108756	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77416178	GGAGGATTAGGAGGT[A/G]TGGCCTTGCCTGATG	78514
rs247111969	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77336173	AACGCTCTGGTCCTA[A/G]GCACTCTGAGAAAGA	78514
rs247112925	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77465007	GAAAATAAACCCTAA[A/C]TGTTTCTGGCACAGG	78514
rs247119256	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77407672	GCAGAAGACAATGGG[A/C]GCTCAGAGACAGACT	78514
rs247121220	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77328293	GACTCTTACATCTGC[A/G]GTTTGTCCTTCCAGT	78514
rs247122949	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77378862	TGAGGACGAGTGAGC[-/T]TACCCCCCCCCCATG	78514
rs247143977	in-del	-/GC			intron-variant	Arhgap10	Mm_Celera	8:77413324	GCATGTGGCAGCCCG[-/GC]TGGCTGCGGAGCTCC	78514
rs247144841	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77272570	CCAGGGGCTGAGCTG[C/T]CCTTCCCCCAGAGGC	78514
rs247162417	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77432668	GACCCTGCCAAAGGT[A/G]ACTAAAGTGTACAGC	78514
rs247163198	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77508711	AAATATTTGGTGTGA[A/G]TACTAAACACTGTCA	78514
rs247166331	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77336747	GGTGAAAACCAGGGC[A/G]GAGCTTCGTCCCGGG	78514
rs247168251	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77317043	CTGATACTTGCCCCA[C/T]CCCTTCCTGCTTTGA	78514
rs247172469	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77431395	GTCCCACCTGGTTTT[C/T]CTAGGGATCACCAAC	78514
rs247175661	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77424651	ACTATTATCCTCTGG[A/G]TGCTATGTCAACAAA	78514
rs247181840	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77367203	AAATACATGGCTTAA[A/C]CCCTTAGAAGAATGG	78514
rs247204121	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77309978	AAACAAACAAACAAC[C/T]CAGCAAGCATCTTAA	78514
rs247209493	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77477023	CTATGTTGAAGCCCT[-/A]CCCCCCTTCTCCCCA	78514
rs247217410	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77317388	TAAGCTGGGTAACAG[C/T]TTTCTAGTAGCAAAC	78514
rs247217612	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77471518	GCAAAGAGAGGCCCA[C/T]TGGACTTGCAAACTT	78514
rs247221853	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77439743	AAGCAAATCCACGAT[A/G]AACTCTGAGAGGAAA	78514
rs247226547	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77431610	AACACATGGAAGCCT[A/G]GGGCGTGTGGGAAGG	78514
rs247228226	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77430859	GAGGAGAGGAGAGGA[A/G]AGCAGGCGAGAAGCC	78514
rs247238697	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77436406	GGCCATGACAAGAGA[A/C]CCGGCTGAATGCCAT	78514
rs247263422	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77477920	CCTACAGTCACTTGT[A/G]TCCTTGGTTCAGTGA	78514
rs247267207	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77365783	CTACAGGAGGGAATC[A/G]GGTTAGGTGAGAAAA	78514
rs247267942	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77378164	CGGGAACCTGGACAA[G/T]TCTTCTTCCCCTGTA	78514
rs247272756	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77452463	GGATTAAAGGTGTGC[A/G]CCACCGCTTTTAACA	78514
rs247279288	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503766	TCCGGAAGTCACTTC[A/G]GGCAGGAGCTACCCA	78514
rs247302907	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77321136	GCCCCCTGGGCCCTG[C/T]CTTCCCCACCACGCT	78514
rs247316131	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77265840	GTGAGGTGTGTGTGC[C/T]CAGCCCAGCTTGTCT	78514
rs247321021	in-del	-/TG			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484428	AACGGGACAGGACAC[-/TG]TGCAGCACACTGCAC	78514
rs247324753	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77396298	GAGAGCAGCAGGCAC[G/T]CATAAAGATGAGCCC	78514
rs247326251	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77378606	ACTGAGAGCCAAAAA[A/G]ATTTACTTATTTGTT	78514
rs247328949	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77458183	AGGTGCACGAAGGAC[A/T]CTTTCTAAAGGTTCA	78514
rs247329111	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77278506	AACAGTACTAACATG[A/G]CCTTGATTTTCCTGG	78514
rs247333037	in-del	-/ATAT			intron-variant	Arhgap10	Mm_Celera	8:77407427	TAGATAGATAGATAG[-/ATAT]AGATGGATGGATAGA	78514
rs247337625	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484023	TCTAACCTCACTCCT[C/T]CCTTCCTCTTGCTTC	78514
rs247343719	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77448559	CCTCTGTTCCCTTTC[A/T]CCACCTTCATTTCTC	78514
rs247353242	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77411642	AAGGTGACTCAACGT[A/G]TAAGTTACTTATAGC	78514
rs247355362	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77345905	GAGAAAACACAGGTT[C/T]CAAACACTGTTCTTC	78514
rs247364418	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77279137	ATATTGCTTGTTTTT[A/T]CTTTTAGCTAAGCCA	78514
rs247367165	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77272440	GGTACTGAGACCCTA[C/T]ACAAACAACTGAGGT	78514
rs247373103	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77341568	CCACGCCTCCTGTCC[A/G]GTGCTCTGTACTCAC	78514
rs247377868	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77491124	GGGCTAGAGAGATGG[C/T]TCAGCGGTTAAGTGC	78514
rs247379615	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77293230	ATTTCCAACCCCAAG[A/T]TGGAGGCCTGCTCCC	78514
rs247380584	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77371058	AGCTAGCTATATTAT[C/T]ATACATGAAAGACAT	78514
rs247381225	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77472261	ATGTACTGCTTATGG[A/G]ACTATAAATTAGTAT	78514
rs247388995	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77380695	ACAAAAAAACAAAAC[-/A]AAAAAAAAACCTCAA	78514
rs247392289	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77344543	GGAATAAATTCACAG[C/T]GATGACGAGACAGCA	78514
rs247421711	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77412097	TTTAATTTCCCAACT[A/G]AGAAGCCCTCTGAGC	78514
rs247429617	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77342137	AGACTGTCACAGAAC[A/G]CGACAACTGGACACA	78514
rs247429780	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77291677	GCTCCAGAGCCAGAC[C/T]GCCTGGTAGTCCTGG	78514
rs247437719	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77363250	ATCTTTCTCTGTGGC[-/T]TTTTTTTTTTTTTGG	78514
rs247452604	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77441535	CTCCTATACTATAAT[A/G]AAAAGTATTATTACG	78514
rs247461483	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77272663	TTTCTCTTCCCACTC[C/T]CCTCTGTCTCTCTCC	78514
rs247466411	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77337756	ACTCCTGGCAAATTC[A/G]TCCGCCTCCCTTGTA	78514
rs247470706	in-del	-/ACAC			intron-variant	Arhgap10	Mm_Celera	8:77415389	GCAGGCAGACTTGGG[-/ACAC]ACACACACAGAGGCA	78514
rs247478502	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77284515	TTGTAAGAACAAAAG[A/G]GAGATTAAGATAGTG	78514
rs247481032	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77323466	ATTTAATCTTTCTTT[C/T]GTACACCTGTTTATA	78514
rs247486763	in-del	-/AG			intron-variant	Arhgap10	Mm_Celera	8:77473681	AACTAAACCTCCCCA[-/AG]AGGAGCTCCTGACTG	78514
rs247489704	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77405672	ATACAGATAGATGCT[C/T]TCTAACCGAGAAATG	78514
rs247489912	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77447768	CTCTTATGAAGTTAA[A/G]CATTAAGCTGGGGCT	78514
rs247500219	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77499798	AATATATTAGCTTTA[A/T]GTCTAATAGAGTCCC	78514
rs247502220	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77412678	TTTTGACGGGTGCTG[A/G]GGATCTCAACTCGGA	78514
rs247512940	in-del	-/TTTTTGTT			intron-variant	Arhgap10	Mm_Celera	8:77514702	CCACAGTTTAATTGG[-/TTTTTGTT]TGTTTGTTTGTTTGC	78514
rs247520740	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77489243	ATTCTCACTTTCTCC[C/T]TCTCTCTCTCTGGTG	78514
rs247543256	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77383159	AGGAAACCCACAAAT[C/G]TGCTCGAAGGCTTTC	78514
rs247545929	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77317562	CAGCTCTCATTTGTC[C/T]GTGTGAGCACTGACT	78514
rs247545949	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77324001	ACCCCCCCCATCCCC[A/T]CCACCCCTTCCATAG	78514
rs247547023	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77254080	GTCCTGTGAGCAGAC[A/C]CAGACACAGAAGAGC	78514
rs247551009	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77327597	CAGTGGCTCTGAAAG[-/C]CCTTCACACAGCCCT	78514
rs247558927	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77265710	ATCTGCCCAGGTCTA[C/T]CACAGGGACAGAGAG	78514
rs247563133	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77505429	TGGAGGTCAGTAATG[C/T]TCCTCTTCAAATTCA	78514
rs247563384	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77499236	GGCATGTAATGAATT[C/G]AAAGCTAACCTGGAG	78514
rs247584714	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77496520	CCCCCTCCTCCTCCA[C/T]GATGCTTTTTTTCCC	78514
rs247589713	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77352683	AACACACACACACAC[A/C]CCCCAAATAATGCCA	78514
rs247606580	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77383558	ATCACTATGCTGAAA[A/G]TGAATTTCAATGGTG	78514
rs247617463	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77498180	TGTGAGCTGAAATAA[A/G]AAATAACAGCTAAAG	78514
rs247623155	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77305363	GGGACTTTTGGGATA[C/G]CATTTCAAATGTAAA	78514
rs247626025	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77504802	AGCATGGTCACAGTG[A/C]GAGCATGGCACACTG	78514
rs247631455	snp	G/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77502688	AATGACCAAGTGGGT[G/T]AGGGTCTGTGGCCTG	78514
rs247645303	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77399889	GACATGCGCTAGTAC[-/T]GTGTGCGATCTGAGA	78514
rs247648729	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77254703	TTGCCTACATTATAA[A/G]AATGAATTACACTGT	78514
rs247659047	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77453943	GGGGAAAGCCTTCCT[A/C]ATACAGAGCCAAGCC	78514
rs247665754	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77384508	GGCAGGATGAGGAAG[C/T]CTAGAAGCAGAGGAC	78514
rs247677834	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77439200	GTCTACGGTGTGTAG[A/G]TCTGAAAATCAGCTA	78514
rs247690778	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77508461	GACAATCAAAGGAAT[C/T]TAGGACAGAGATTTT	78514
rs247690955	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77257717	GATACACAAGGCATG[C/T]TTACTTGTGAGCACT	78514
rs247696870	in-del	-/TACAGTG			intron-variant	Arhgap10	Mm_Celera	8:77464898	GTGTCTGAAGATAAC[-/TACAGTG]TACTAGTATACATAA	78514
rs247700524	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77366036	AGTTACAGCTTTCTC[C/T]GTGCTTGCTTTCTGC	78514
rs247705717	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77359008	AATGGCAGCAAGTCA[A/G]TGGGAGAGGGAGTAA	78514
rs247711278	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77453558	GGTTTGTGGGCAAGT[A/G]GAACCGTGTCACAGA	78514
rs247727491	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77279292	TTCCCTTTGAAAGAA[A/G]GACTGGCGCTTCCTG	78514
rs247728295	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77288092	GACACATAAAGTACT[A/G]TGGGCCAGGCAGTGC	78514
rs247740304	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77516155	AGTCCATGGATGTCC[A/G]CACACCTCCCTGCCT	78514
rs247752016	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77400593	AGAGGACATGAGATT[C/G]TCTAGTGCTGGAACT	78514
rs247756502	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77331597	ACAGTCAGGCTGAGT[A/G]GTGGAGAACAGAGAC	78514
rs247758865	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77279965	TCCTGGTGCAGAGCA[C/G]TGAGAGGGACACAAG	78514
rs247759923	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77359882	AGGGAGTCCCAAATC[C/T]ACCCAAGTTCCAGAT	78514
rs247760193	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77258624	GATAAGGATCAGAAA[A/G]GGAGAGTAGATTCCC	78514
rs247765039	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77459432	GACAGCCATTCAGAC[A/G]CACTGGCTTCACCTC	78514
rs247766840	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77439205	CGGTGTGTAGGTCTG[-/A]AAATCAGCTAAGGAC	78514
rs247779674	in-del	-/TTTTTTT			intron-variant	Arhgap10	Mm_Celera	8:77365475	ATTTATTTACTTGGG[-/TTTTTTT]TTTTTTTTTTTTTTT	78514
rs247784137	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77288948	GCCACATGCCTTTAC[C/T]CCCAGCATTCAGGAG	78514
rs247785469	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77374679	GTGAATGAAGCAAGC[-/A]AAAGGCAGTACTCTA	78514
rs247794167	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77259703	GTACGAGCACTGATT[A/G]CTCTTCCGGAGGTTC	78514
rs247806183	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77413185	AGTGGCCGGGGCTGA[G/T]AAGGAATGGGAAGAG	78514
rs247814601	in-del	-/CACT			intron-variant	Arhgap10	Mm_Celera	8:77288474	ACACACACACACACA[-/CACT]CTGCTTTCTTCCAAG	78514
rs247815716	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77370989	ACAAAGAGAAAAGTC[A/G]AGCACTTGTTTAGTT	78514
rs247825966	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77371767	TTGTATATGTGGTGT[-/G]GGGGTCCTCGCTGGC	78514
rs247845088	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77325713	GGCAGTGAAGAACGG[C/T]ATTTCTCCAAAGATT	78514
rs247845507	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77383225	AAAGGTTTAAGAAAG[A/G]TTTTTGTTAAATGCT	78514
rs247845575	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77509009	TATATATACACGTGT[A/G]TGTGTGTGTGTATAA	78514
rs247847536	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77293168	GGTACCCAGAGCCCA[C/G]TGCTGCAATATCAGA	78514
rs247865059	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77338081	AGTCATGTCTGAATG[G/T]AAACCCAAAGCATGG	78514
rs247876235	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77477503	CTAAACCTATAATGT[A/T]TTTAGGGAAAGGTCT	78514
rs247876494	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77373964	CCAAAGGCAAGACCA[C/T]ATTTCTGTTGTGGCT	78514
rs247880764	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77285894	CATAATGGTAATTAT[A/G]TGAAAATGGATTAGA	78514
rs247891280	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77354380	TCCCTTATTCCTAAC[-/T]AAAAACAAATGTGCC	78514
rs247894346	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77383721	AAAAAGGGGAAGACC[A/G]GGAAGAAGGAGAGGA	78514
rs247905697	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77270598	CCCAGCATGGAGGGA[A/G]AGGTGAGTATGAAAT	78514
rs247926488	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77477747	CACAAAATATTGCTT[A/G]GAAAATTACACCATG	78514
rs247927535	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77332200	CCGACTCTGCTGGCT[A/G]GTGAGCCATTTTTAA	78514
rs247933267	in-del	-/G			intron-variant	Arhgap10	GRCm38.p3	8:77297325	TGGAGAGATGGCTCA[-/G]CAGTTAAGACCACTG	78514
rs247935688	in-del	-/AAA			intron-variant	Arhgap10	Mm_Celera	8:77356173	CTGTCTGTGATTATT[-/AAA]AAAAAATGTACACAG	78514
rs247948654	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77419764	AAAAACCATGACTGA[C/T]GGTCAGTCAGGAACG	78514
rs247957536	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77441812	CCAGGAATACTGGAA[A/G]CATAGCGCTCCTTTA	78514
rs247962921	in-del	-/CT			intron-variant	Arhgap10	Mm_Celera	8:77367776	TCACATTCAAACAAA[-/CT]CTCGAGCATTTATGA	78514
rs247964698	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77286546	CAGTAGCTGGAAGCT[C/T]GCACATTGAGAGGGA	78514
rs247966870	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77340450	AGCTGATCTCATGCC[-/G]GGGGACTATTCTGTC	78514
rs247986834	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77476896	TCTGCCTGCTAAGTG[A/C]CGTGGGTACCAGCCT	78514
rs247987249	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77462933	GAATAGCACTAAGAA[C/G]AGCAGAGGCTTCCAG	78514
rs248000257	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77278742	AGCATAAGACAAATC[C/G]TGGGCCCTGAGTAAG	78514
rs248026263	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77365413	ATGAGACCATGCTGA[A/G]GCACAGCCTGATGTA	78514
rs248044716	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77314168	AGCAGTGCAAAGACT[G/T]TCCCTTCAACACGCA	78514
rs248045595	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77417694	AAAAGAGAGAGAGAG[A/C]ATAAGATGAATAGCC	78514
rs248046881	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77364211	GCAAGTGACAAAGGG[C/T]AACTTTTCCTGGGGT	78514
rs248054105	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77258729	TCAAAGTATTAAAAA[A/C]AAGTCATCTGGATGG	78514
rs248063292	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77290318	CATCCCTACCACTTG[C/T]AAAGATCAATGGAAG	78514
rs248075823	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77322420	AAGCAAGCTTACTAA[C/G]GAGATGTAGGCCAGG	78514
rs248085215	in-del	-/CTTGG			intron-variant	Arhgap10	Mm_Celera	8:77342384	GAGAAAAACCACAAA[-/CTTGG]CTTGGCTCTAAAACA	78514
rs248091381	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503844	CCACCCAACTATGGT[A/G]GCCTAGAGTTTAAAT	78514
rs248097431	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77395771	CCACCCTAATTTCCA[A/T]CAAAGATAAGCCAAT	78514
rs248124085	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77259938	TGAGAACAGGGTTAG[A/C]TTGGATGAACAAATG	78514
rs248125963	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77446995	CTTCTTCCAGCAGCT[A/G]CCCCTCTTCTCAAAT	78514
rs248144091	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503314	AATTTTAAAATTGTC[C/T]TTCTGAAACATTTGT	78514
rs248149669	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77396233	AAAAGCCAGAACTAC[A/G]GAAGCAATTGTTAAA	78514
rs248160024	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77375581	CCCAGGAACTCAGGG[G/T]AGCCGTTCCCCTTTG	78514
rs248169707	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77449063	CACTGCCGCATCCCT[A/G]GCCCTGTGCACACTG	78514
rs248198290	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77421172	GAAGCTACGGCAGGA[A/G]GACATGTCCAGGGCT	78514
rs248201627	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77337362	CTGAAGAGAAACCTC[A/T]GAAGACTTCGCAGCT	78514
rs248225305	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77464117	TGTTAGGAACTGGAC[A/G]CACCAGTCAGGAGAA	78514
rs248233642	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77404858	GTAGACCAGGCTGGC[C/T]TTGAACTCAGAAATC	78514
rs248236614	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77459101	GCTTGATGAAAATTA[A/G]CTTTACGTGGCCTCT	78514
rs248238365	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77464775	GGCTGGAGAGCTGGC[A/T]CAGCGGTTAAGAGCA	78514
rs248250460	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77409448	AAACACAACAAGGGC[A/G]CATTTTTCTAGTTCA	78514
rs248250637	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77428047	AAACCAATGGCAAGG[A/C]GCAATTGTTTCTTAT	78514
rs248253499	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77427322	TCTGCCTGCAGAGAT[A/G]ACAGAGAAGCCGCTG	78514
rs248260699	in-del	-/TT			intron-variant	Arhgap10	GRCm38.p3	8:77389207	CACATCCTACTCATA[-/TT]GTTTCTTTTTTTTTT	78514
rs248271234	in-del	-/AATATCGGGCC			intron-variant	Arhgap10	Mm_Celera	8:77295577	TTTTCAAATAAACTG[-/AATATCGGGCC]AAGAAGTGGGAGTGG	78514
rs248284159	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77386424	TGGTGAGATGGCTCA[A/G]TGGGTAAGAGCACTG	78514
rs248300811	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77464425	GCAAAGGCAGCCAGT[A/G]ATAGAACCTTCTTGT	78514
rs248303110	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77399353	AGTGCCACTTCTCCT[C/T]TCTGAGTCTCCACAG	78514
rs248306715	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77365590	TGCCATAAACTCCAT[C/T]GAAATGAATAAATAA	78514
rs248314264	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77409949	AAAGAGCAAAGTCCA[C/T]ACCTGGGATTCTCTG	78514
rs248314399	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77427721	TGTGGCCACTCGTGT[G/T]CTGCCCACCTGCAGG	78514
rs248314440	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77435191	TTTAAGCAGAGAACC[A/G]ATAGAATGATTACAT	78514
rs248323288	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77342692	AGATGGTAGTCTAAT[A/G]ATGTATTTTTCTGAA	78514
rs248325645	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77441749	ACCCTCCCCCCCCAC[A/C]CACACACACACATAC	78514
rs248330946	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77514046	TGACTCTCCTCTCCA[A/G]AGCCCCTCCCAACCC	78514
rs248339256	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77290162	CCAAATAAACACACT[A/G]GGGAATGCTGATGAG	78514
rs248346115	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77297353	CTGGCTACTCTTCCA[A/G]AGGATCCAGGTTCAA	78514
rs248347545	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77414835	ACACACACAATGCTA[C/T]ACAGAGAAACCCTGT	78514
rs248351625	in-del	-/ATGT			intron-variant	Arhgap10	Mm_Celera	8:77438432	TGTGACCCTTTCTCC[-/ATGT]AGCTGGCTGCTCTCC	78514
rs248369302	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77320015	TAGTTGAAAATCGAA[A/T]TTTGGATGGTCTGTT	78514
rs248369664	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77313458	GCTTCCATGACTCTC[A/C]CAAAACTTAGACTCA	78514
rs248374586	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77265687	GCCATGACTGGTGCC[A/G]TGGAGCAATCTGCCC	78514
rs248378670	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77434698	GGGTACCACATGATC[A/C]CAAACAGCCACCTTA	78514
rs248412798	in-del	-/AGTCTCA			intron-variant	Arhgap10	Mm_Celera	8:77473953	ACGTGAAACATCTGG[-/AGTCTCA]AGTCAACATCTGAGG	78514
rs248417025	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77344383	AAAGTGCTCAATTAG[C/T]TATTAAGTTAGACTG	78514
rs248419176	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77351687	CTGGAAAAAAAAAAG[-/A]AAAAAAAAAAAAACA	78514
rs248434060	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77468613	ATGAGAGGAGATGGA[C/T]GTGACTATGGGCCTG	78514
rs248444230	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77512756	ACAAACACAGATGTA[A/G]TTAGTTCATTACTCT	78514
rs248446141	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77330269	ACATAGAAAGAATGG[A/G]GGAACACAACACAGA	78514
rs248456983	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77282272	GAAACACCATTACCA[A/T]AGCAAGCAGGGGAAG	78514
rs248465970	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77308605	AGAGGACTTAAGAGG[-/T]TTTTTTTTCCTACTT	78514
rs248483202	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77445732	GGAAGAGAGGAGAGC[A/G]GCCATGCCTGAGAAT	78514
rs248490527	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77273831	TATTCCTCAGAGGGA[C/T]ATCACACTGTGAACC	78514
rs248491646	in-del	-/C			intron-variant	Arhgap10	GRCm38.p3	8:77471817	GCACACAAGTTAAAA[-/C]CCCCACAAAGAATGA	78514
rs248502942	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77474502	TCTGTGTCATACGTA[C/T]ACACATTGTGTCACA	78514
rs248518627	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485843	AAGCACTATGAAGTG[C/T]CCAGTCCTCTAGGGC	78514
rs248530111	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77269264	ACTCAGAACCCAGAG[A/G]CCACTTACTGTAATC	78514
rs248538215	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77460990	CCTACAACACAACAA[A/T]GACAGAGGGGGTTCT	78514
rs248542519	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77318569	ACCAGCCTCTTCTCC[A/G]GTGTGAGCTGTATTA	78514
rs248542691	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77338241	GTGAGAATGTGCAAG[A/C]ACTCTGAGTAAAACA	78514
rs248554962	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77398317	GTCAGTGCTCTTAAC[G/T]GCTGAGCCATCTCTC	78514
rs248561697	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77263424	AAAACTTTGTTTTGT[A/G]CAGTTAACACACTCT	78514
rs248563050	in-del	-/TT			intron-variant	Arhgap10	Mm_Celera	8:77331225	AAAAAAAAAGTTGAC[-/TT]TTTTTTTTTTCCTTG	78514
rs248571785	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77459549	GGGTGTCTCCATGTC[A/G]TCTTGGCTGTCCTGG	78514
rs248594524	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77319785	TTTGGAAAGAAGCCT[G/T]CCTATTCTACAAGCA	78514
rs248608549	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77480637	GTATGTACATCTGTG[A/G]ACCAGCTATGTGCCC	78514
rs248611700	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77348740	TGCCCTGACTCCTAA[C/G]TTAGTTAGTTGTCTC	78514
rs248629992	in-del	-/ACAACA			intron-variant	Arhgap10	Mm_Celera	8:77406913	GTAGGCAGCAGTAAT[-/ACAACA]ACAACAACAACAACA	78514
rs248630987	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77255336	GCTGGCCACCCACAC[C/T]ACAGTGCATCATGCT	78514
rs248634392	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77446963	TCTGCTGGGGTGCCT[A/G]TGGCTGTCTCTCACT	78514
rs248635317	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77470747	TCTGGGGAGTTATTC[-/T]TTTTTAAGATTTGTA	78514
rs248638447	snp	A/C			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494595	TTCTTGTTCCAGCTG[A/C]GAGTTTAAAACCTAC	78514
rs248643281	in-del	-/CCTCTCTAAGT			intron-variant	Arhgap10	Mm_Celera	8:77468287	GTGGGGCCACCTATG[-/CCTCTCTAAGT]CCTCTAAACTCACTG	78514
rs248654633	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77414713	GAGAAAGTTCCAGGA[C/T]AGCCAGGGCTACACA	78514
rs248661533	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77414505	TTCCTCCTAGGGATG[A/G]GGGATCAAGAAACAT	78514
rs248665288	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77351252	CTACAACATCTCCAA[A/G]CCCACCATCTCTCCA	78514
rs248701150	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77412605	TGAGGACCAAGGATG[C/T]CCTCTTCCCCACATC	78514
rs248703639	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77385680	CTCTCAATCTACTCT[A/G]CTCTTCCAGAGACAT	78514
rs248709929	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77256191	TCGATGGAGGTAGCT[G/T]TCTCAGACAGTACAA	78514
rs248718625	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77352245	TATGGCTGAGGGTCA[C/T]CACAACATGAGGAAC	78514
rs248720449	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77343630	CCAAAAAGGCTAATA[A/G]AAACTTTGCCCCAAC	78514
rs248721881	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77500830	CCTTAGTACCCACCA[C/G]CCACATACTAAACAC	78514
rs248727991	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77414137	AGAAGCGAGGAGGAG[G/T]AAGGTCCCACGGGCA	78514
rs248740678	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77512810	GAAATGGCAAGGAGC[A/C]CTGCCAGATAGATCG	78514
rs248753864	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77434919	ATGAGGAGGCACGTG[C/T]TCCACCTGAGTTTCA	78514
rs248755737	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77329156	AGGCAGGCCTCTCTG[C/T]AAGCCGGTCACAGTA	78514
rs248777213	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77419519	CGCCAATTGGCTTTG[C/T]ATGGGTCCTGGGATT	78514
rs248786665	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77500341	GACCGCACTACCCAA[C/G]AGAGCAGTCAGGAGC	78514
rs248786673	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77506504	TGTCAAAGCCACAAA[A/G]CTTCTTTTACAAATT	78514
rs248791707	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77368396	CAGAGCACACAGAGC[A/G]CATGCTAACCATTAC	78514
rs248793088	in-del	-/CGC			intron-variant	Arhgap10	Mm_Celera	8:77422759	GACCAACACCAGGCA[-/CGC]TGCTGCAACAGCCCT	78514
rs248796237	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77380580	TTACCTTTTCTCGGA[A/G]TGCTGATGGCTACAG	78514
rs248818853	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77289589	CCCAAGGTTCTTCCA[C/G]CCCTCCCAACCCCAA	78514
rs248826093	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77402664	CAAAGCATTAGCAAC[G/T]CTGTGAGTTCAAACC	78514
rs248837742	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77456178	TGATTTATTTATAGA[A/G]GAACAAGGCTCAGAT	78514
rs248839213	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77324902	CTATGGCACATGCAA[A/C]GTCTATACAGAAGGA	78514
rs248848838	in-del	-/AG			intron-variant	Arhgap10	Mm_Celera	8:77489211	TATATATATACACAC[-/AG]ACAGACATTCACATA	78514
rs248873822	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77267777	TGTAACACCATGTGA[C/T]TTTTCTCGGAGATTC	78514
rs248874361	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77309706	GCACATGTGCACATG[A/G]AGCAATTCAGAAAGA	78514
rs248882597	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77440836	AAAAAGCCTTGCCAG[A/T]GACTGAAGCCCTAAC	78514
rs248886597	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77369215	CCTGCCTCTGCCTCC[C/T]AAGTGCTGGGATTAA	78514
rs248897873	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77361971	TAGAAGGAGAGCGGT[C/T]ACTCAGAGAGTGCAA	78514
rs248898838	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77325442	CATCTTCACTGGCAA[C/T]TCACACATGGCTGCT	78514
rs248901005	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77319455	GCTAAGAAACAGGAT[A/T]CTTGAATAGTCTTGG	78514
rs248903299	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77455709	AACACCCAGCCTATT[A/G]TGGGTAGTGCCACCC	78514
rs248904808	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77462285	GGAGGAAGAAAGGGT[G/T]GGTCTTCTTAAAATT	78514
rs248917976	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77491670	AGGGGTATGGCCAGA[A/G]CTCCCGTGGCCACAT	78514
rs248924837	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77254484	AAATAAATAATAATT[A/C]TTTTTTAAAAAGAAG	78514
rs248934721	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77439125	GCATTAAAGGTGTGC[A/G]CCACCACTGGCCAGA	78514
rs248937201	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77447142	AAGATAGGGTTTCTC[C/T]GTGTAGCTCTGGCTA	78514
rs248949989	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77262729	CTGCAACAAGGCCAT[A/G]CCTCCTAGCCCTTCC	78514
rs248955574	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77362418	GGTCTCAAGTAAATA[C/T]TGCCTTCTTCTAAAA	78514
rs248956352	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77294325	CTATTTTATAATTTT[A/T]AAAAAATCTACATAT	78514
rs248959181	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77432291	GTAGCTCACTCTTAC[-/A]AAAAAATAGTTGCAC	78514
rs248959721	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77512724	GGCCTAAAACAATGC[A/G]TGGCTCACACGGCAC	78514
rs248966418	snp	A/C/T			intron-variant	Arhgap10	GRCm38.p3	8:77296275	GGAGAGATGGCTCAG[A/C/T]GGTTAAGAGCACTGA	78514
rs248967332	snp	C/T			downstream-variant-500B	Arhgap10	Mm_Celera	8:77250195	TCTTGTGGGAAAGGC[C/T]CCTGCTGCTTCACTC	78514
rs248983757	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77263102	ACCCTCCTAAAACCA[C/T]AGATATTGTAATCAT	78514
rs248985949	in-del	-/GA			intron-variant	Arhgap10	GRCm38.p3	8:77254512	AGGAAGGGGGAAGGG[-/GA]AAGGGGAAAGGGGAA	78514
rs248992585	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77289003	GTTCAAGGCCAGCTC[A/G]GCCTTCAGAGAGCCA	78514
rs249005922	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77511437	AAATGTTTAAGGAAG[A/G]AAGGAAGGAAAAAAA	78514
rs249016008	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77460919	CAGGATTCACAGAGA[A/C]GACACTGGGACAGCC	78514
rs249019282	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77430839	ATGAGGTCAGCACAC[A/G]GGGAGAGGAGAGGAG	78514
rs249022480	in-del	-/AGATTC			intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77493081	GTCTACAAAGCAAGT[-/AGATTC]TGCCAAGGCAACTCA	78514
rs249027924	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77272343	GCAGCACCACCTTCT[A/T]AAGGCTTTGTGTTGC	78514
rs249040313	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77340641	GAATGTATGCCTCTA[C/T]ATGCTGTTGCACACC	78514
rs249046793	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77473240	GATTTATTCTGCAGC[A/G]CCCACCCCAGCACCA	78514
rs249058203	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77480118	CTCCAGGCCACGGCC[C/T]GAGTCCTTGGGGCCT	78514
rs249060048	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77479954	CCAGGAATGAAGCTG[A/G]GACTCAGGAGGACAT	78514
rs249068532	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77289877	AAGACTGCCTAACGG[C/T]CTGAACCTCTCCTCA	78514
rs249079056	snp	G/T			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519571	GGTTTGCCTGCAGGT[G/T]GGCTTTCAGGTTTTA	78514
rs249082901	in-del	-/C			intron-variant	Arhgap10	GRCm38.p3	8:77471647	TCTCCAACTCCCCTT[-/C]CCCCCCCCCTTTTTT	78514
rs249102360	in-del	-/TTAAA			intron-variant	Arhgap10	Mm_Celera	8:77463785	AACTTCTTTGGGTCT[-/TTAAA]GAGTTTTCAGAAAGT	78514
rs249132063	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77420325	AAAGTAGTTCCAAAG[A/G]AGTCACTAGAAATTA	78514
rs249138453	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77361264	GCTGGCACTTTCTTA[C/G]TGAGTCCTTCTTGCA	78514
rs249139060	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77403550	GCAGCTGTGTTGTTA[C/G]TGTGTTTGGTTTTTG	78514
rs249186738	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77262890	AGGAAAGAGCTTGAG[A/G]CTCTTGGAGAATAGG	78514
rs249186829	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77368064	AAATGGCACATTAGA[A/C]ATCCGGTCTTATAGG	78514
rs249189184	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77383490	ACTGTGGCATTGGTG[C/T]TGGCTTCATGGGGAT	78514
rs249206036	snp	G/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485602	TTGAACTCACCTGAA[G/T]TAACCTCCATTTCCA	78514
rs249211361	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77506100	CCCCCCCCCGCCTCT[A/G]GAACGCTGACATTAC	78514
rs249212661	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77419466	CCAACTGAGCCCCTG[A/T]GAGTCCTTTTCTCCT	78514
rs249222052	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77398144	GTGATGGCACTACTT[C/T]TTTTTTTCTTTTTTT	78514
rs249222096	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77404198	GAAATGTCTAAGCAT[C/T]GGCACTGCACAGGGA	78514
rs249225742	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77287138	CCTCAAATACTATTG[C/T]CATTGCTTATTCATA	78514
rs249232405	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77263321	GTGGGGCTGTTGGAG[A/G]AACAGAAGAAGGGAG	78514
rs249233112	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77470992	ATTTATTATATATAC[A/G]TAAGTGCACTGTAGC	78514
rs249240948	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77378128	TTCATTCAAACACCA[A/G]CACCTTTATTCCCTG	78514
rs249243004	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77515586	CCCTTTTATTCTTGA[A/G]GGGAAGAGTGTAAAG	78514
rs249249951	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77437230	TATTCTGATCCACAG[C/T]AGCTGTTTGAAGAAT	78514
rs249257381	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77513302	AGCATCATCCCTAAG[C/T]ACCCCGCTCATGAGT	78514
rs249261760	in-del	-/GG			intron-variant	Arhgap10	Mm_Celera	8:77473168	AGAAACGGCTCAGCA[-/GG]GAGAGCACTGAGGAG	78514
rs249265800	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77295738	TATATGACAAAAGTT[G/T]TTTTCAATTGCTTTT	78514
rs249271761	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77333635	AAGGCAGCGTTGACA[A/G]AAACTTCCATGAACC	78514
rs249273611	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77346539	AAAGTATCTTCGTCC[C/T]TCTACTTTTCAGGTA	78514
rs249275934	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77505773	CTGCCGTAGTACTCC[A/G]CACACAATGTCTCAC	78514
rs249279904	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77339152	ACAAAAAGTTTTATG[C/T]GAGCAACGTTTTATA	78514
rs249282561	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77398536	GTAGTCGGTGTGCAC[A/T]GGAACGCCCAAATGC	78514
rs249294182	in-del	-/AAGAACCCTGGGT			intron-variant	Arhgap10	Mm_Celera	8:77455175	AAGAAAATTCAGGGC[-/AAGAACCCTGGGT]AAGAACCTGGAGGCA	78514
rs249298175	snp	C/T			intron-variant, missense	Arhgap10	Mm_Celera	8:77476629	ACTCTCAACACAGGC[C/T]GAACCAAGTATCTGC	78514
rs249309461	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77436284	AATTGAGAGATGGCC[A/G]TGGACGTGTCTCCAT	78514
rs249313036	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77278444	CCCAAAGAACTTATT[A/C]AATATTGACTTCCCC	78514
rs249324223	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77352849	ACCCACGACTGCAGG[C/T]CCAGATTTGAATCTC	78514
rs249336731	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77406231	GTATAAAAGAAGTAA[C/T]ATATGACCTCAACTA	78514
rs249341396	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77373411	TCAGCCTGGGCTAAC[A/G]CACCACAGACCTGGG	78514
rs249358808	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77359609	AAAACAAAACCAAAA[A/C]ACCCTTAAGTGGGTG	78514
rs249371015	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77467787	GCAGACTGACCCTTC[A/G]GACAAAGGAATGCGA	78514
rs249371029	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77461030	TACACCCCTCACCAA[C/T]ATCACCAGCACCCAC	78514
rs249371757	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77443104	CTCTAACTCCCAAGT[A/G]CTGGGATTAAAGGTG	78514
rs249373043	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77372464	AATCTCCTGAGTTGT[C/T]TGGAGACTGAGAGTA	78514
rs249378555	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77315551	GAGGCTCAAGTTTTC[C/T]TTCTGTACCCTTCAT	78514
rs249378695	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77272971	AGAAGGAAGGAGGAT[A/G]GACAGAAATCAGACT	78514
rs249381591	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77454163	TCAGCTAGCATTTCG[C/T]CTCCCGGAGCAGCAT	78514
rs249396597	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77374137	AACCATACAACACTT[C/G]TATAATCAATTCTTG	78514
rs249397432	in-del	-/GGAC			intron-variant	Arhgap10	Mm_Celera	8:77451333	GAGAGGGGGAGGGAG[-/GGAC]GGAAGGCGGGAAATC	78514
rs249410246	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77347694	GATGGAAGAACGCTA[-/G]CTTTGGAGCCTACCG	78514
rs249411175	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77497310	TCTGCTACAGCAGCC[A/G]GTGCCTTTAACTGCT	78514
rs249414918	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77423185	CCTTCAGAGGGCATA[C/T]GGTCACTGAAGGGAG	78514
rs249417728	in-del	-/TG			intron-variant	Arhgap10	Mm_Celera	8:77466321	ACAGTAAAAGAGGTC[-/TG]TGTCGCCAGACTTTG	78514
rs249419592	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77353277	GACCAAATGATCAAT[A/G]AGCTCTACGTTCATG	78514
rs249428193	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77467432	GGCAAGCCTGGTCTA[C/T]AGAGGTCTACAGGTC	78514
rs249446912	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77253314	AAGTGCTCCCCTCTC[C/T]AGCACTGGAATGGTG	78514
rs249458040	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77382371	TACAAGCCGAGGGCA[A/C]AGGCTAAGAGAAAAC	78514
rs249458497	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77368762	GAGCAAAATGAGTTC[C/T]CATTCAAGCCTAATC	78514
rs249461772	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77418291	TACATTATAAAAGGA[A/T]GGAATGTGAGGACGG	78514
rs249467004	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77373063	CTCTCTGTAATGGTC[-/T]TTTTTTTTGGGAAGG	78514
rs249467229	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77306864	CTACAAAGGATAACA[A/G]ATGGAAAACTCCAAC	78514
rs249471658	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77253611	CTGAAAGTGCAACAC[A/G]GGCCCCATGCAAAAT	78514
rs249480392	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77429285	CCAGACCCGAGGGTG[C/T]CCACCCCCCTCAGCT	78514
rs249494107	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77460550	TCAGCCTACAAGCAT[A/G]ACACAGACCTTGCAG	78514
rs249501504	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77268448	AAGCAGCAAAAAAAC[A/G]CTACCCCATTTTTCA	78514
rs249506027	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77461136	TCTAAGACACCTTGT[C/T]GGGAAGTAAAATGAA	78514
rs249512114	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77402558	CTTGAGAGGCAGGCA[A/G]AGAAGTCTGAGGCCA	78514
rs249513294	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77315849	AGAACTTAAAGTATA[C/T]AAGAGTATATGAGAG	78514
rs249514119	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77472143	ACATATATATATATA[C/T]ACACACATATATATA	78514
rs249531926	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77504664	CCAGCATGGTCACAC[A/T]GCAAGAATGGCACAC	78514
rs249533087	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77332136	ACAGAGGTTCCTGCT[A/G]TAGCCGTTAGCGGAC	78514
rs249536509	snp	A/G/T			utr-variant-3-prime	Arhgap10	GRCm38.p3	8:77250608	GGACTTTCGAGAGTC[A/G/T]CGCAGTCCCCCTGAA	78514
rs249550645	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77460264	AGAGGATCCACGGTA[C/T]ACAGCCTCAGCACAA	78514
rs249554738	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77496183	TATTTTCAAAGGTTT[A/G]CCTGCCTGATGTTTT	78514
rs249555513	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77354326	CTACAACCCAGAGAA[C/T]TAGCTGTCTCAGCCC	78514
rs249556235	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493779	AGCATCCCATACTGC[C/T]AACACTTGACCACAG	78514
rs249560142	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77345200	GCGGACCTTGCCAGA[C/G]TGAAGGACAATTCTG	78514
rs249580459	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77275909	AAGTTGACTTCACTG[A/G]CTTAGATCTGCATTC	78514
rs249585736	in-del	-/CCCA			intron-variant	Arhgap10	Mm_Celera	8:77292756	GTTAGATACTCCCCC[-/CCCA]CCCTTTGTTCTCCCA	78514
rs249595429	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77467540	CCATCAAAGCCAGCT[C/G]TAAGGCTCTTTGATT	78514
rs249600375	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77396950	GGCACACAGGTAAAA[G/T]GATGTTTTGCTAAAG	78514
rs249600854	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77364938	CAGGAACGTGGATAA[C/T]CTCAGCCTCCGCTGA	78514
rs249616130	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77501728	CCTCCTCCTTTCCTT[C/T]TCTTCCCTTCTCACT	78514
rs249616902	snp	A/G			intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77492996	TAGTTGAGTAGTGGT[A/G]GTATACATTTTTAAC	78514
rs249621550	snp	A/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77345792	ACATTTGCTATAACC[A/G/T]GTTTCTTTTCTCCAT	78514
rs249623289	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77271397	TAAGCTGAGTAAACC[C/G]TTTCCTCCCCATTTG	78514
rs249632540	snp	C/T			intron-variant, downstream-variant-500B	Arhgap10	Mm_Celera	8:77358272	TGAGTTCTCAGCTAC[C/T]GTTGCAGCGCCATAC	78514
rs249639583	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77511139	AAAAGGCCTCACGGG[A/T]GACATAATTCTTATC	78514
rs249640770	snp	A/G			utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250610	ACTTTCGAGAGTCAC[A/G]CAGTCCCCCTGAAAA	78514
rs249641729	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77346798	TCACTTAGGTGCCTC[A/G]GGAAGGGGCAGTTCT	78514
rs249647051	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77257802	ATGACACCTGCAGTT[-/C]CCACGGCACTCTGGA	78514
rs249659884	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77415460	TCACATTCTCACTGG[C/T]TAGCATATGCATATA	78514
rs249662842	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77294044	CTGAACAGGAATCGT[A/C]TTGCCAAGAGAGCCC	78514
rs249664599	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77326081	TGCTGGACAATGCCA[A/T]CCCATCACAGACATG	78514
rs249673063	in-del	-/AC			intron-variant	Arhgap10	Mm_Celera	8:77472180	CACATATATACATAT[-/AC]ACACACACACATACA	78514
rs249690278	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77460273	ACGGTATACAGCCTC[A/G]GCACAAACACTGCTC	78514
rs249696021	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77461509	GTTAAAAATGAGCCC[G/T]TTTTCAGACTGCCAG	78514
rs249714895	in-del	-/AG			intron-variant	Arhgap10	Mm_Celera	8:77388176	AAGCAAATGAAAAAT[-/AG]AGAGGCCACTCTGAA	78514
rs249715116	in-del	-/GA			intron-variant	Arhgap10	Mm_Celera	8:77413458	GGCTCACAACCACCC[-/GA]GACTCTTCAGATCGA	78514
rs249719138	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77508100	CAGTGGGCCAGGCAC[A/G]GCTGGCTTGATCCTC	78514
rs249722858	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77421482	GCCAGGTAAAGCAGT[A/T]AGCCAATGCCTGCGC	78514
rs249723882	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77448083	ATTTCAACCAATAAG[A/T]ACATAAAAGATCAAT	78514
rs249727782	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77381272	ACTAGATGAATCCTC[A/T]TGGCTTTCTCAGCCT	78514
rs249729091	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77326599	ATCAACCCACTGTAC[A/G]TCCTAATTCCTGTGC	78514
rs249730056	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77298237	TCACTGTAATCATAC[C/T]CTAACTATTCTGGTT	78514
rs249733818	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77422784	AGCCCTACTCTCCTC[A/G]TATCAACACCAGGCA	78514
rs249739546	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77410481	AGCTAGAGGCCTACC[A/T]TCCTCACTCAGCCAG	78514
rs249767772	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77283106	CCTCCATGTTCCTCA[C/T]TCTTAAATAGTAACC	78514
rs249775858	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77465897	GAGAGTCCCAGGCTA[A/G]AGAAGTGGCTCAGGG	78514
rs249778191	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77448366	ACAAACACTAGTTGA[A/G]CCTGTCAGTGCATGC	78514
rs249780490	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77251758	GTAGTAGCCACACAC[-/C]TGGGGATGGGGGATT	78514
rs249783137	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77507511	TCATCAGTTCCGTAT[A/G]AGACATGCATGGGTG	78514
rs249783415	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77327783	GCACTTCCAGTTATG[A/G]ATGCTCTAAGATTCA	78514
rs249783815	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77509223	CAGCCACACCTCCTC[A/G]CTACCACTTGCTCCA	78514
rs249791464	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77320989	AAGGAATTTGCAGAT[C/T]GGGTTAACTCACGTG	78514
rs249807877	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77331356	ACCGTGGCTAAGTCA[G/T]GTCCGCTCTCTAAGC	78514
rs249816708	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77288726	ACAGCCGCCCATATG[C/T]TCATCAGACTGAAAT	78514
rs249817240	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77287942	AGAGAAAGAGAAAGA[A/G]AAAGAAAAGCCATTC	78514
rs249818273	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77417580	ATTAAAAAATAAAAT[A/G]TAACCAGGGTTTTCT	78514
rs249825163	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77272217	GTTTTGTATAGCGTC[A/G]CAAACACTACCTGAC	78514
rs249838503	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77479042	CTGGCTCTGCTCAGG[-/C]CCGCCCTTCCCTCAC	78514
rs249838872	in-del	-/AAG			intron-variant	Arhgap10	Mm_Celera	8:77310922	TGGGTGTCCGTGAGT[-/AAG]AAGACCTGTGCACTG	78514
rs249841147	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77354172	AATGTTTGTATTAGT[A/G]AAAGGATAAAATATG	78514
rs249844098	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77442328	TTTCTCTCCTCTGCA[G/T]GTCTCCTAACAGAGC	78514
rs249855404	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77447459	TTCACTCCAAGGAAT[A/T]CAGAAACAGACCATC	78514
rs249859969	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77388591	ATAAAAGAAAAATGA[A/C]ATGGGGATGAAGCAA	78514
rs249863909	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77290814	CAGGTGTGACAGCAA[A/G]GCTGCTAAGACTCCC	78514
rs249868588	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77266193	GTGTGTGGTTTCACC[C/T]CCCTAAACACACTCC	78514
rs249880558	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77261655	TATCTGGACACTTGG[-/A]AAAGTCCAAACACCT	78514
rs249882261	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77416910	TCTGAGACTAAGCAG[A/C]ACAGGTCTGTGAGCA	78514
rs249884122	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77517020	CACTGACCCTTTCAA[C/T]CCCTAATCTTTGAAC	78514
rs249899532	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77346651	CCCCTGAAAAACACC[C/T]TTTCTAGTAAGCTTG	78514
rs249901864	snp	C/G/T			intron-variant	Arhgap10	Mm_Celera	8:77354642	GTCTAGGTGGCAATA[C/G/T]AACTTTAAAAACAAA	78514
rs249906000	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77291465	CACACATCTATTAAC[A/G]TAACTGTTTGCATGT	78514
rs249906309	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77283774	ACCTGAGAAGTGCAG[A/G]ACAGACAGACAGCCA	78514
rs249906495	in-del	-/ACACACACACACACACACACCA			intron-variant	Arhgap10	Mm_Celera	8:77273118	CACACACACACACAC[-/ACACACACACACACACACACCA]AATAAATGTAAATGT	78514
rs249918949	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77452835	GTTCACTTCCCAGTC[A/T]CTCACATGGCAGCTC	78514
rs249924893	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77376165	CTCCAGGGTTAAGGG[A/G]TGTGAAGAAAACCAC	78514
rs249942296	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77312545	AGCAAGGTGCAGGTG[C/G]CAGCCATCCTTGTGC	78514
rs249944895	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77256353	CTGTATGTGCATATG[C/T]CATGGTGATATGTTG	78514
rs249961518	in-del	-/CCAG			intron-variant	Arhgap10	Mm_Celera	8:77348868	GAGGTTTCTAAGTAC[-/CCAG]CCAGCGCCAGGCACC	78514
rs249965505	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77345231	CCAAGTTGTTCCCGC[C/T]AAGGAGAGACCTCAT	78514
rs249974986	in-del	-/AAACCAAA			intron-variant	Arhgap10	Mm_Celera	8:77511789	CTGTCTCAAAAAAAC[-/AAACCAAA]AAAAACAAAAACAAA	78514
rs249978610	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77491594	TAGATACTGAACCCA[C/T]CCCACCAGGGTGAGC	78514
rs249999456	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77284256	GTATGAAACCCTCCA[C/T]ACTACATTCAAACAA	78514
rs250008895	in-del	-/GGGTCAGGAATGTGA			intron-variant	Arhgap10	Mm_Celera	8:77434976	CTGAAAGGTGTGAAG[-/GGGTCAGGAATGTGA]GGGTCAGGGGGAGCA	78514
rs250010197	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77292689	TCTACATAGGCTAGC[C/T]ACCTGCCACGACCTC	78514
rs250011043	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77415937	AAAAAAAAAAATATG[A/G]CAGATGCTGGCCAGT	78514
rs250025063	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77259429	CTCCATGTTTGTGGA[-/G]CAGTTGACCCTGTCT	78514
rs250037034	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77285177	CCTGGTCTACAAAGT[A/G]AGTCCATAACAGCCA	78514
rs250052297	in-del	-/TTTT			intron-variant	Arhgap10	Mm_Celera	8:77327675	AAATTTGTATGTGCA[-/TTTT]TTTTTTTCTCCCTCA	78514
rs250053032	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77451558	TGAACCATGCGGCTT[G/T]GTGGAGCACACGTGC	78514
rs250062447	in-del	-/AC			intron-variant	Arhgap10	Mm_Celera	8:77346851	TGATGATGTATGACA[-/AC]GCATGCCGACAGAAG	78514
rs250080185	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77328221	CTGACCATCCCCAGA[C/T]TTTGAAGACAAGTTA	78514
rs250117278	in-del	-/ACCCCC			intron-variant	Arhgap10	Mm_Celera	8:77420960	GAGAAGAGCTTGATG[-/ACCCCC]ACCCTCAAAGACTGA	78514
rs250126160	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77264678	ACACAGACACACACA[C/G]AGAGAGAGAGAGTCA	78514
rs250126932	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77449773	ACAAAGTGATCTTGG[A/G]CAGACCATGTGGATC	78514
rs250131636	in-del	-/GCCA			utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250914	GACCCCCCACGGCCG[-/GCCA]GGAGCTACAGGAGCT	78514
rs250132234	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77305860	CAAGAACATAAACAA[C/T]AGAACCCAAGGCTAC	78514
rs250133907	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77376188	AAACCACAGATAAAC[-/A]AAAGGAGGAAGAAAA	78514
rs250137197	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77427060	CAACCCTAAGACCTT[C/T]CAGGGAAGTCATCGG	78514
rs250144324	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77354868	AAGCAACCTCCAGAT[-/A]AAAATCACTTCACTA	78514
rs250144706	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77516032	CTCTGACCTCCCACG[C/T]GTACAATGGCTCAAA	78514
rs250147572	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77399896	CGCTAGTACGTGTGC[A/G]ATCTGAGACCTGAGT	78514
rs250148653	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77487481	GCAAGAGTTCCAGTG[C/T]TTATGAGCCACCTGA	78514
rs250155408	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77469847	GATTCCACCAGGCGT[A/T]TGCTCTTAAGTGCCC	78514
rs250163855	in-del	-/TAAA			intron-variant	Arhgap10	Mm_Celera	8:77286821	CCCATGTCAGCAAAC[-/TAAA]TAAAGTTACTAAGAA	78514
rs250168500	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77458323	GTTTGGCCTTGGACA[A/G]TCCAGAATCATCTCC	78514
rs250179422	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77433436	cacacacacacacac[A/T]cacacacacacacac	78514
rs250182705	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77378006	GGAGCTTAGACCTCA[C/T]CGCTTCCGGTCACTC	78514
rs250204397	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77433913	AAGAATACAAAACAC[A/G]CAACTGTCCCCTCAA	78514
rs250206945	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77388012	CTCAAGTTGCCTTTA[C/G]TGAATCCCGAACCCC	78514
rs250207037	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77400333	TGGGGGGAGAGAGGG[C/T]CCTCAGCTACTTTCC	78514
rs250211592	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77292280	AGGCCAACCCCAGAC[A/T]CTCCTCTTCCTCAAC	78514
rs250239925	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77475479	AGAGGACCCAGTTTC[A/T]GTTCCCAGCACTCAT	78514
rs250241943	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77363036	TGCTCAATGTGACTG[A/C]AAACACACCATTTTC	78514
rs250246633	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77293114	AAGAACCATGGCATG[C/T]TCTGAGGGGTGGTAA	78514
rs250249145	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77265319	TGAACAGCTGTCCCA[A/T]CCAAGTGTTTGAAAA	78514
rs250258004	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77319172	TGGGTAGGGGAGTAG[C/G]GGGGAGGGTATGGGA	78514
rs250266295	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77489662	CTAACTCTGAATGTT[A/T]CCGAAGGCTGTGGTC	78514
rs250293606	in-del	-/TATG			intron-variant	Arhgap10	Mm_Celera	8:77414767	ATTTGTTTATTTGTT[-/TATG]TGTTTATTTATTTGT	78514
rs250294119	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77370812	CAGTCGACTTCGTGC[A/G]GACCGACAGGTACAT	78514
rs250295249	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77356839	TGGCACCACTGTGAC[A/G]GGCTACTTAAATAAG	78514
rs250296773	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77406198	GTCTTGGAGACCCAC[A/C]CCTAAAAGAAGGAAA	78514
rs250300434	in-del	-/CT			intron-variant	Arhgap10	Mm_Celera	8:77319918	GAGGCTGAAAACGTC[-/CT]ACCTCAGGCTCAGGT	78514
rs250319592	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77370105	TTCACAATCCTGAGG[A/G]GGGGGGGGGCGGGGG	78514
rs250331221	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77385583	GAAAATCCTCCATGG[A/G]GAACCTGTGTGAGGA	78514
rs250334734	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77422662	TCTAGAACTCAGGAA[C/T]GTGGGTGGTGGGTGG	78514
rs250344509	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77431434	CAGAAACTCCCCATA[C/T]GGTACTGACCAAGAA	78514
rs250346089	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77374445	CAGGAAAGCCTTGCC[-/A]CAGAGCCTTCTGATT	78514
rs250350028	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77405437	ACAGAGGCCAGAAGA[A/G]GAAGCCAAATCCCCT	78514
rs250356039	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77341546	TAAGGCAGCCCTTCA[A/C]TCACAGCCACGCCTC	78514
rs250362763	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77401016	CCGACTCGAGTCTCC[A/G]CCAATGTTCAGTGTC	78514
rs250364614	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77269885	GGTCTAAGAAGGGCT[A/G]GGTATATGTAGGTGG	78514
rs250366003	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77474178	AAAGATCTATGGCAT[C/G]AGTCGTTAGCACCTT	78514
rs250376348	in-del	-/CAGAAA			intron-variant	Arhgap10	Mm_Celera	8:77343125	TGCTCAATGGTCCAG[-/CAGAAA]CAGTCAACACCTAAG	78514
rs250378716	in-del	-/CG			intron-variant	Arhgap10	Mm_Celera	8:77397655	GCAGTGGTGGTAACA[-/CG]CGTGACAGGTTCTGC	78514
rs250380569	in-del	-/AGGCAACTGAGAG			intron-variant	Arhgap10	Mm_Celera	8:77419289	GTGTCTCAGAAGATC[-/AGGCAACTGAGAG]AGGCAACTGAGAGAG	78514
rs250399170	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77422079	CCTGGCCTCTGACAC[A/G]TCATTCTTGGGGGTG	78514
rs250403654	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77509002	TTTAATATATATATA[C/T]ACGTGTGTGTGTGTG	78514
rs250404357	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77421511	GCAATATTCGAATGG[C/T]TAAAATAAACTGGAA	78514
rs250408584	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77406062	TTTAAAAAGTTACTC[A/G]GCCAGGCGGTGGTGG	78514
rs250410621	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77400649	TAGAACTGAACCCGG[A/G]TCCTCTGCAAGGGAA	78514
rs250414664	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77335687	TTGTGAGCAGGTCTC[A/C]GAGGGTTTGGGCAGT	78514
rs250418186	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77305989	GATGATAAAGGACTT[G/T]AAGAAGGGCATAAAT	78514
rs250428368	in-del	-/CTTA			intron-variant	Arhgap10	Mm_Celera	8:77425332	ATTCCTTTCTGCTTG[-/CTTA]CATACTGAGGAGGAG	78514
rs250431484	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77480074	CGAAGAAGAAGGAAC[C/T]AGAAAGAGAAGCAGC	78514
rs250432841	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77481501	TACCTTAATCACCAA[C/T]ACTCCGTTTACAATA	78514
rs250435795	in-del	-/TA			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77502874	GAGAGAAGCATCACC[-/TA]TATGTATGGGCATGA	78514
rs250440013	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77516919	TTTGAATACAGATGG[A/G]ACTGAGGTGGCCAGC	78514
rs250440361	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77508463	CAATCAAAGGAATCT[A/G]GGACAGAGATTTTTA	78514
rs250442175	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77270412	AACCCCAAATCAACT[C/G]CCCCCTCACAAGGCT	78514
rs250460254	in-del	-/ACCTCTTGAAT			intron-variant	Arhgap10	Mm_Celera	8:77265739	AGGGAAGCATTGAAC[-/ACCTCTTGAAT]ATCAGGAAGGCTTCC	78514
rs250472159	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77281004	CGAGCTCTCTACCAC[A/G]GGGTCCCAGCCCCAG	78514
rs250487751	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77373909	CAGCCTTTCTCTGCC[A/G]GGCTTACTTCCATTC	78514
rs250488283	in-del	-/T			intron-variant	Arhgap10	GRCm38.p3	8:77511628	TCCACTTTAGTTTTA[-/T]TTTTTTTTTAGGACA	78514
rs250504452	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77375966	ATCAAGACCACTAAC[A/C]TGTAGCAAAACATTT	78514
rs250504474	in-del	-/AT			intron-variant	Arhgap10	Mm_Celera	8:77476419	ATCATCTCTGGACAC[-/AT]GTCCTTTAAATGTTT	78514
rs250505570	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77341902	AGGAAAAAAAATAAA[A/C]ATAAAAAATACGAAC	78514
rs250513430	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77273666	TGCACCACAGATGCA[G/T]GAGGGGATGAGCACA	78514
rs250514511	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77375524	CAAATCCTATCAGTT[A/C]ATTCTGCTGCTCGTT	78514
rs250537920	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77439428	TGTTCATCGATTTCA[A/G]TCCTAAATTCCAATT	78514
rs250540910	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77332034	CCTCGGGATCTCTAC[A/G]ATGGGAACTGACATA	78514
rs250545417	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77470676	CCGAGAATTTAGTTT[C/T]GAATGGTAGTGTAAG	78514
rs250553663	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77442391	TGTTCACTTCAGTGC[A/G]CTACAATTTCCTCTC	78514
rs250558537	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77317497	GAAACCTCTTCCAAG[C/T]ACACATGCAAGGTCT	78514
rs250560868	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77275027	ACAGGGGAACGCCAG[A/G]GCCAAGAAGTGGGAG	78514
rs250561251	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77262579	CGATGGCAGGAAGCA[C/T]GGCAACAGGCAGGTA	78514
rs250570143	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77342347	TTTCATCTAGTTAGG[C/T]TGTGTCCAGCCACAG	78514
rs250571031	in-del	-/CT			intron-variant	Arhgap10	Mm_Celera	8:77438287	TCCCATGTGTCTTCC[-/CT]CTCTCCAGGGCCTCA	78514
rs250571591	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77500295	ACTGGAAGGGGACAT[A/G]GTGTGAACCTCGAGA	78514
rs250576471	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77375858	GCTAGTGAGGCCCCG[A/C]TTTAGAGTCCACGGT	78514
rs250579805	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77371398	GTTTTCTGTCTTTTG[A/C]CCAGATAATTAGCAT	78514
rs250585337	in-del	-/ACACAC			intron-variant	Arhgap10	Mm_Celera	8:77489515	CACACACACACACAA[-/ACACAC]ACACACACACAAGTG	78514
rs250598701	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77446306	CTTTGTGCGCTCCAA[C/T]GACACGATCGTATCT	78514
rs250600110	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77438781	AGAAAGAATGACACC[A/G]ATACCTAACACCTGC	78514
rs250606533	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77374525	AGCATCCCCTTCCTT[G/T]TATAGGGAAGAAAGG	78514
rs250606922	snp	C/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77470022	CCAACGGCTGATATT[C/G/T]GAAAGCACTGTTTGA	78514
rs250622454	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77310955	GGAGTAAAGCAGAGT[C/T]CAGCCACAGTAGACT	78514
rs250637489	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77326089	AATGCCAACCCATCA[C/T]AGACATGCATTCTTG	78514
rs250640081	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77487847	CATCTCCAAGCCTTT[-/G]GGTCAACATGAGGAC	78514
rs250640109	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77270529	ACAGGGCAAATGTAC[A/C]GGTGAGCTCCCCTCG	78514
rs250641954	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77275735	TCAAATGTACATGAA[G/T]AGGAAGCTGGGGAAT	78514
rs250649133	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77255023	AACTCTGCACTGAAG[A/G]TAAAAGTGTGTAGAG	78514
rs250657924	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77271315	CATCGGCTCCTGCCT[C/T]CAAGTTCCTGCCCTG	78514
rs250660349	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77445413	AAAACTGTTTGGGTG[A/G]GAAGGTCTGCGCTTA	78514
rs250674017	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77271137	TGAGGAAATGCCTCC[A/G]TGAGATCCAGCTGTA	78514
rs250689318	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77490105	CATTGCAAACATACT[A/G]AGCTGGGAGTCAGCA	78514
rs250709921	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77496885	TGCTAGAACTAAAGG[C/T]GTGCACCACCACATC	78514
rs250726134	in-del	-/TT			intron-variant	Arhgap10	Mm_Celera	8:77297833	GTATACTCTTTTGAC[-/TT]TTTTTTTTTCTTTCC	78514
rs250729589	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77463109	GCTAGCAAAGTCTAC[A/G]TGAGACTAAAGGTTT	78514
rs250735818	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77351210	GTAATGTCCATATAA[A/G]TGTCTGCGTGTGAAA	78514
rs250744074	in-del	-/AA			intron-variant	Arhgap10	GRCm38.p3	8:77414910	CACACACACACACAC[-/AA]ACACACACAAACACA	78514
rs250746231	in-del	-/GATG			intron-variant	Arhgap10	Mm_Celera	8:77374714	TGAGGCTCACATGCA[-/GATG]GACAATTGTCCCTAC	78514
rs250771840	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77496380	TGAGAGATCCTCCCA[C/T]CACAGTAAGGACCAA	78514
rs250789943	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77297777	ATACAGATCTTGTGC[A/T]TATAAGTTATAGTTT	78514
rs250799336	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77462813	GCCTGGCTTTTTTTT[C/T]CTCTCCTCATAGATA	78514
rs250799378	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77469578	ATGTACTGGGCTGGA[A/G]GGGTATCTCAGCAGT	78514
rs250805012	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77447163	GCTCTGGCTATCTTA[A/G]AACTCTCTCTGTCAA	78514
rs250807366	in-del	-/T			downstream-variant-500B	Arhgap10	Mm_Celera	8:77249937	TGCCTGGGCCTGGAG[-/T]TTGCACTTCGAGCTG	78514
rs250819670	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77252512	AGGACTGGACCAATT[A/G]CAAAGCCATGCCCCA	78514
rs250832166	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77381510	CCCACACGTGAGTAT[-/G]GGGGCCGCCGGACTG	78514
rs250836195	in-del	-/CAT			intron-variant	Arhgap10	Mm_Celera	8:77259496	TCAACTTTTCCTCAC[-/CAT]CTTCCTGCTTTGAGT	78514
rs250836962	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77477219	AAGACATTAGGATTT[-/AA]AAAAAAAAAAAAGAC	78514
rs250846589	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77290912	TCCCAGCAATTATCA[C/T]ACAAAGGACTTAGCC	78514
rs250851559	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77349364	TAAACTCACGTACTT[A/G]ACAGAAGATGATAGA	78514
rs250852120	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77368481	CACTGGTGCAGAAAC[A/G]TCTGTGTAAGGTCCT	78514
rs250855188	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77468438	AGGGCGGTGTGAAAT[C/T]GTGTCTCTGTCCTTC	78514
rs250863011	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77254772	ATGAGCGCAAGAAAA[C/G]AGCCTTGGGTCTCAG	78514
rs250864579	in-del	-/ATA			intron-variant	Arhgap10	Mm_Celera	8:77417506	CTGACAAAATTAACT[-/ATA]ATGTCATAAAGATAT	78514
rs250867061	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77251400	CATGCAGCACTTTAC[C/T]TGCGACCTAGAATGC	78514
rs250870422	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77464395	GTGGACATTCTTTGA[A/G]GTAGAATGAGAAGAG	78514
rs250876791	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77488239	ACAACCTCTCAGGAT[A/G]CTCTGAGCCTCCCAG	78514
rs250885403	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77408168	AGGCTGCAGCTTACA[A/T]TCATGTAAAGATCAC	78514
rs250887946	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77429994	CACCCACACTCTGCA[C/G]TTATTTACAGAACCT	78514
rs250890558	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77424736	ACGGACAGAAAGCAG[C/T]TTTATGCTTTTGTTG	78514
rs250908284	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77361943	GGGGCAAGGAAGGAA[A/G]GTGGCTTCGCCCTAG	78514
rs250911975	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77510770	CTTAATGTCCCTAAG[-/C]CTCAGCACAGCCATG	78514
rs250924345	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77322299	CATAAAGACAGCAGA[A/G]GGGTTCATGTGGACA	78514
rs250927455	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77433358	GCCAAGAGGAGGGAC[-/A]TGTGCACGCATGTGT	78514
rs250935660	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77397059	TTGCTTTGCTCTGCC[C/T]CACTATTTTTCACTG	78514
rs250941405	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77451286	GAACTGATCACCACC[A/G]CCACCATCACACCTC	78514
rs250945725	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77312328	CTATGACCACACTTT[-/G]ATAACAGCCCCAAAC	78514
rs250954734	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77329448	ATGGGAGACTGGGAA[A/G]AGAAGATGAGTCAAA	78514
rs250956845	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77323348	ATTTCCCTCCTTCCC[A/G]CTCATTTTGTACATC	78514
rs250964131	in-del	-/G			intron-variant	Arhgap10	GRCm38.p3	8:77486714	ATCTGATAGACAAAA[-/G]GGCCCCCCTCCCTCT	78514
rs250994194	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77356926	CAGGAAATAAAAAGC[C/T]ATGCTCTATAACACC	78514
rs251002912	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77384050	CTTCCCAAGTGCATG[A/C]GTCCTGAAGAGCGAG	78514
rs251008967	in-del	-/ACAGACAT			intron-variant	Arhgap10	Mm_Celera	8:77411411	CACATGTGTACACAC[-/ACAGACAT]ACACATGCATACACA	78514
rs251017102	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77339927	TCCTCTTTTATCACT[G/T]CTGCTAAGTCTTGAC	78514
rs251020876	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77499514	GATGGGAAGGGAGGG[-/T]TAGGGGAAGATCTTG	78514
rs251031213	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77412646	GAGCATGGGATACTC[A/G]TGAGGACACCTCAAC	78514
rs251052699	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77357409	AAATGTGGATTCTCA[C/T]GCACTCATGGGAGCC	78514
rs251053042	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77350495	TGAACACAACTGTAT[C/T]CTGGCCTTTCTTTCT	78514
rs251061548	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77455654	GATAGTACTTCAGGC[A/G]AGCTGGTAGGGCATT	78514
rs251065242	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77287321	ACTAGGTGACTTCCC[C/T]GGTTGGGTTTGGCAG	78514
rs251069096	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77269981	CAGTACCGCATAAAA[C/T]GGGGCAATCAAGAAA	78514
rs251076149	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77499215	CACAGCATGAAGGGA[A/G]GGGAGGGCATGTAAT	78514
rs251077771	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77334350	CAGTACAGGAGAAGG[A/G]AGTACAGTCCAGGAA	78514
rs251080818	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77397553	AGTTGGAATTGGAAA[C/G]TGTGGGCATGCGCAC	78514
rs251084842	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77427859	GGCTCACACAATTAT[C/T]CCTCCGCGTTTATTC	78514
rs251098392	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77475150	TGAGCAGAAGAGAGG[A/T]AGGGGGGATTCAGTA	78514
rs251114286	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77335790	GAAAAGGAAGTGACT[C/T]TGAGTTCTAAATTTT	78514
rs251115763	in-del	-/GT			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519530	GGGGGGAGGGAGGGG[-/GT]TAGGTGGCATGGCTT	78514
rs251120834	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77451712	ATAGCATGAACTTTA[-/T]TTTTTTTTAAAAAAT	78514
rs251130556	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77470769	AGATTTGTATGTTAT[A/T]TATGTTATATTGTGT	78514
rs251138747	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77447122	ATTTTGTTTTGTTTT[A/C]ACCCAAGATAGGGTT	78514
rs251142877	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77514628	CTAGGAATCCAACTC[C/T]GACCCTCTGGAAGAG	78514
rs251144992	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77509452	TCAGAAGGTAAGCAT[-/C]GAAAGGAGGAAGAAA	78514
rs251146337	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77294557	GAATGGTGGCTGAAA[C/G]GACCTCTCCAGGATC	78514
rs251170147	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77360527	TTACCACAGCTGACC[A/G]CAGCAGGCAATGAAC	78514
rs251183721	in-del	-/AT			intron-variant	Arhgap10	Mm_Celera	8:77328432	AGTGCTGCTTTGAGC[-/AT]GTCTGTTTTCTTAGT	78514
rs251188727	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77446919	GTGTAATTTAACACC[A/G]TATTCTTGTTCTGGG	78514
rs251215305	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77454632	CCCAACTAAGACATA[C/T]ACACTCAGTACAGAT	78514
rs251224840	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77316195	GGCACGCTGTGTCTG[C/T]GCGTTCTTCCCACAG	78514
rs251225128	in-del	-/GA			intron-variant	Arhgap10	Mm_Celera	8:77465751	AAGTCATTGCCTGAT[-/GA]GAAAAGCCAATCAGT	78514
rs251225978	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77330768	CAGATGCAGGGAGTA[A/C]TATAGTGGAGATTGT	78514
rs251247014	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77451900	ACAAATTCCTCACTG[C/T]CCAACTTGGCATGAT	78514
rs251249948	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77311212	AGTATTAAAACACTA[A/G]GTACCCTTTAAGTTC	78514
rs251251109	in-del	-/AAAAA			intron-variant	Arhgap10	Mm_Celera	8:77341727	TCTGAAATGTCTATC[-/AAAAA]AAAAAAAAAATCCCT	78514
rs251260161	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77260344	ACAAAAGACTGGAGT[C/T]TAAAGGACATGTCAA	78514
rs251271863	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77491418	CCACAATGAGTCACT[A/G]GTCTGGTTCGAGGCC	78514
rs251279569	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77416873	CCAAATCCCAGGCTT[-/A]ACCAATTAAGAACTT	78514
rs251282057	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77357626	GGAAGCTCCTTTACC[A/G]AAGATAGGAAACAAC	78514
rs251289039	in-del	-/TTTG			intron-variant	Arhgap10	Mm_Celera	8:77277444	CACCTGTGGATTTGC[-/TTTG]TTTGTTTGTTTGTTG	78514
rs251295431	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77254123	CCTGACTAGCAGATC[C/T]ACCAACAGAATGTAT	78514
rs251301265	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77266618	TATAACTTTTCTGTA[A/G]ATATTAAACTATTTC	78514
rs251323089	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77402451	AGACAGCCAGCTACA[G/T]TATACTTATATACAT	78514
rs251327127	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77490907	GCTCTTTATTCTTAG[A/G]TGTGTGGTGCTAGGA	78514
rs251343662	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77295635	GGGGGGGAGGGTATG[A/G]GGGACTTTTGGGATA	78514
rs251362201	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77309055	CAGATGAATGCCTGA[A/C]TCTGATCACCTCCAC	78514
rs251362895	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77437270	AACAGTGCCTATCGA[A/G]TCTCAAATCTACTTT	78514
rs251377221	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77296171	CCTGGATGCTACCAT[C/G]TTCCCACCTTGGTGA	78514
rs251397845	snp	C/G			intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77492825	AAGTGCTAAAGCCTT[C/G]CCACTAGCTCACTCT	78514
rs251416644	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77305937	CTCCAACACACCAGG[-/A]AAAGGAAGACTCAGA	78514
rs251423224	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77335385	AGAGCTTTTCACTGA[C/T]AGCCTTTGCACCCCT	78514
rs251432917	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77377882	AGAAAATGGCAGAGA[A/G]CACAGGGTGTCCTAA	78514
rs251435156	snp	A/C			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519298	GGCTGCAGTAATCCT[A/C]GATCCCATAAGCTGA	78514
rs251451699	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77425865	AAAGCCAAAAACAGG[A/C]CTAGCTGAGTCTACT	78514
rs251463545	in-del	-/GTACTAACCTCCATTT			intron-variant	Arhgap10	Mm_Celera	8:77313255	GACTCAGAACAAATG[-/GTACTAACCTCCATTT]GTGACAGTGATGCAT	78514
rs251473862	snp	G/T			upstream-variant-2KB, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77518039	CTGCTCTCCCGCCCG[G/T]GCGCCTTCGGCTCTC	78514
rs251488781	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77372429	AGAACCAAGCCTATT[A/C]TATAATGTACTTGCT	78514
rs251498509	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77411500	CATGCACGCACACAC[A/G]TACACACATACACAT	78514
rs251504010	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77431764	AAGTTCACAACCCAA[A/G]TGCTGTGTGGAAAAA	78514
rs251516046	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77403051	CTTTCCACGCCACCT[A/C]ATGCTTCAGGAACAC	78514
rs251518020	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77408350	CGATTCATCTGTGTC[A/G]ACGATTTAAGCAGAA	78514
rs251526000	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77366804	CTGAACCATATCCCC[A/C]GCTCTTCCTTATTTA	78514
rs251528032	in-del	-/AACTTAA			intron-variant	Arhgap10	Mm_Celera	8:77407794	ACAGGAGAGAAAAGT[-/AACTTAA]AGAGCAGTAAGAGAG	78514
rs251532883	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77425051	CTGGCCAGGCGGGTC[A/C]CACCAACAGGAACTC	78514
rs251554145	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77291374	CTGCCTTTTGGTCCT[C/T]CTACTTTAAAATCTT	78514
rs251555126	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77272145	GAGTCTGAGGATGCC[A/G]TGTTTCTGTGTAGCT	78514
rs251558214	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77431114	TGCATGCACACAGAC[A/G]CACGCACGTGTGCAC	78514
rs251561350	in-del	-/AA			intron-variant	Arhgap10	GRCm38.p3	8:77509608	AGGTTTATACCTTAC[-/AA]CTTAAACCAAAATAA	78514
rs251578504	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77375018	CCCATCCTAATCCTC[C/T]GGTATCTTTCCTATA	78514
rs251579402	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77310185	ATAGCCTGGTTGGAC[G/T]GGAAAACCACCACCT	78514
rs251581457	snp	C/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484261	CTGAACACGGGGCCT[C/G]ACACACGCTAAATAC	78514
rs251589395	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77266160	CAAGGCTCATGCTGC[C/T]ATGCTGACCGTGGGC	78514
rs251592484	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77468030	GACCCTCAACGAAGC[A/T]GACCCCAAGTCCCTT	78514
rs251597179	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77330842	TGAACATATACAGAA[C/T]TGTTCTCATTTACAA	78514
rs251618295	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77378463	GTGGAAGTCTTCCAC[G/T]TTGTTTTCTTTGCTT	78514
rs251621238	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77434727	TAACCAAACCCGCAG[C/T]TCAGTAAACTATTAT	78514
rs251626831	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77307524	AGACCATTTCATCCT[-/A]AAACAAAAGGATATA	78514
rs251629170	in-del	-/AG			intron-variant	Arhgap10	Mm_Celera	8:77306863	CCTACAAAGGATAAC[-/AG]ATGGAAAACTCCAAC	78514
rs251635811	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77325522	TACGACAGAAAACTG[-/C]CCCCTTGCCATAGTC	78514
rs251635911	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77253503	AAGCACAGCAGAATC[A/G]AGTGTTGGGCCTCTG	78514
rs251636870	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77404573	TCCAGAGAAGCTCTT[-/A]ACTGCTATTTTAGAC	78514
rs251647274	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77475987	GAACAGGACTATAGC[A/G]TAGCTGCAGGTCTCC	78514
rs251657588	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77278898	GGCAGTAAGCATCAG[A/G]AATAACTGACTGGAC	78514
rs251668703	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77382811	CAAACAGTTAGAAGA[C/T]GTCAAGGGCAGGTAG	78514
rs251671211	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77274297	TTCCTTTTTAATTTA[A/T]TTTTTTCATTTTTTA	78514
rs251676469	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77378915	GAGAGTACAGAAGGG[A/C]GGGGCTACAGCGAAG	78514
rs251677665	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77474034	CCCCCCAACCTGGCC[C/T]GTCTTAGATCTCTGT	78514
rs251693858	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77442266	TGGCCAAGAAGAGGT[G/T]AGGAAAAAGACAAAG	78514
rs251698027	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77403671	AGGCCTTCTGGTCAT[-/G]GCGTGAGGAAAAGGT	78514
rs251706486	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77472532	GACAGCTACAGTGTA[C/T]TCATTCATTCATTAA	78514
rs251708741	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77285580	CATTAATAAAGGAAA[C/T]GGAGAGGGAGTAACC	78514
rs251733471	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77345627	TCTCTCCTTGCAATC[C/T]TGCAGCTCCAGGAGC	78514
rs251739060	in-del	-/CACACA			intron-variant	Arhgap10	GRCm38.p3	8:77385234	CGGGAGCTCCTCGAG[-/CACACA]CACACACACACACAC	78514
rs251743107	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77272571	CAGGGGCTGAGCTGC[A/C]CTTCCCCCAGAGGCT	78514
rs251745772	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77279352	CTGCAAGGGAGCGAG[C/T]GAGCACACATTTGTG	78514
rs251765191	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77478273	TCCCAAGTGTACAGC[A/G]AGGAGGGAAGAACAA	78514
rs251766912	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77474384	AAAGCACTTCATGTA[-/G]GGGGAAACTTTTTTA	78514
rs251774454	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77447924	AGCCTGAGCATAGCA[C/G]ACCTCAAAGCCCGAC	78514
rs251777019	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77272920	GCACAGACTAATGCC[G/T]TGGAAAGCCTCAGTA	78514
rs251777246	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77451502	CAAAAGAGCTACAGA[C/G]CCATCGCCTCCATTT	78514
rs251785359	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77376830	CACCCAAACACACCT[A/C]CAAAGTTTAATAATG	78514
rs251785737	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77459474	AGAGGTCAGGGATCT[C/G]GGGCAAGGGCCAGGC	78514
rs251786157	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77349448	AAGGAGGACTCTCAC[A/G]CCACAGAAGAGAGGG	78514
rs251786589	in-del	-/TT			intron-variant	Arhgap10	Mm_Celera	8:77354213	CATGAAGAAAATCTA[-/TT]TTTAAAAAAAGCTAT	78514
rs251803823	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77502411	CCCTAGAGCTGAACC[A/G]CAGTGACTTATATTC	78514
rs251809445	in-del	-/CC			intron-variant	Arhgap10	Mm_Celera	8:77363494	GGAACCTTGGGTTCA[-/CC]CCGTTTAGACCTATT	78514
rs251809771	snp	A/G			intron-variant, missense	Arhgap10	GRCm38.p3	8:77491974	ACCTGTTCATCATAG[A/G]GTCGTCCACTGCCAC	78514
rs251809860	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77499489	GCCCTGCGGGCTCGG[C/G]GCACAAGGAGATGGG	78514
rs251812161	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494045	GTTAAAAAGGAGGAC[A/G]CAGACATAGTGCTAT	78514
rs251812531	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77384378	TCCTCAGCCTCACTG[-/AA]AAAATGCCTGAAGGC	78514
rs251817645	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77296333	TTCCCAGCAACCACA[C/T]GGTGGCTCACAACCA	78514
rs251832771	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77253904	AATTATTCTACTCGA[A/G]CCCTTTAGTGTTCAA	78514
rs251835495	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77379975	ACAGACTGGCTTCCA[C/T]CTGACTGGCACTAGG	78514
rs251844612	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77447713	ACTGCAGGCACTCTG[A/C]CGTGTGTCTTCGTGA	78514
rs251854485	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77354111	GGTGCAGCTCACTTC[A/G]AATCAATTATACTTC	78514
rs251856841	in-del	-/CT			intron-variant	Arhgap10	GRCm38.p3	8:77486726	AAAGGGCCCCCCTCC[-/CT]CTCTCTCTTTCCCTC	78514
rs251868452	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77315078	CACAGCTACTGAATT[C/T]CACCGTGCGCTAGTT	78514
rs251881562	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77258344	ATAGAAACCCTCACT[A/T]AGACAGAAGCCATAC	78514
rs251893886	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77251825	AATGCAGCTTGGGAT[C/G]ATAACCAAAAGGAAT	78514
rs251912186	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77259818	gcaacagtgtgctta[A/T]taataataataataa	78514
rs251915032	in-del	-/ATAT			intron-variant	Arhgap10	GRCm38.p3	8:77411609	CACACACACACACAC[-/ATAT]ATATACACATACACA	78514
rs251918984	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77383827	CCCTGCTGCGGGACA[C/T]CTGTCAGCATCCGGG	78514
rs251928022	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77500857	ACACTATCATTCATA[C/T]CAATCCCGCAAGGCT	78514
rs251928895	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77358654	TGAACAGCAAGGGGG[A/G]GAAAAAATTAAAAAC	78514
rs251939070	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77414019	GGATCTGAAAATAAT[-/C]ACTCTTTCCAAGCTA	78514
rs251960054	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77463664	GCTTTAAGTGTGCAG[A/G]GTTGGAGGGCACAGA	78514
rs251967582	in-del	-/CA			intron-variant	Arhgap10	Mm_Celera	8:77377721	GAAACAGTAGATTCT[-/CA]TAAACAAAATAAACA	78514
rs251980025	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77308972	AAGCTTAGCACAGAG[A/G]TAGCACCTCTGTAGA	78514
rs251981853	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77471873	ATAGACACTGTGAAC[A/G]TAAGCAAGAGCCCTG	78514
rs251985773	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77506527	TACAAATTCACCTCT[A/G]TTTTTCTAGACACAA	78514
rs251992606	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77254136	TCCACCAACAGAATG[C/T]ATTTCTGGGATTCCT	78514
rs252003883	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77409497	CTCATTTTCAAAACC[A/G]TACTTTCAAATTCAT	78514
rs252005095	in-del	-/CCCA			intron-variant	Arhgap10	Mm_Celera	8:77378145	CCTTTATTCCCTGGG[-/CCCA]CAGCGGGAACCTGGA	78514
rs252007427	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77325340	GATGAGTCTCCTGAC[C/T]TAAGCACTTGGTCCG	78514
rs252011934	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77453770	ATCTAAATGGGCCCT[A/G]ACTGTCCAGCCAAGG	78514
rs252035602	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77332456	TGTGGGGAAGAGACA[-/G]CATAAGAAAGCCTGA	78514
rs252051244	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77471382	GAGCTAGAGAAATTA[C/T]CCAAGGAGCTAAAGG	78514
rs252062352	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77319677	TGCTAGAATGGGCTA[G/T]AGGGTATCTAGTGCT	78514
rs252069292	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77253131	CTCCTCTGAGTGTAC[A/G]CTCAGACCAGACTGC	78514
rs252086356	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77360140	GAGACCGTAGGCAAC[A/G]TACAGAAGAGACCCC	78514
rs252087948	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77481815	GTCTCTATGTGAATT[C/T]CCCAGAATTTCTTCT	78514
rs252089366	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77264672	ACACACACACAGACA[C/G]ACACAGAGAGAGAGA	78514
rs252095147	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77421053	CACACACACACACGC[A/G]CACGCATCCACACAC	78514
rs252095322	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77427757	ACACCGGCAGCCCCA[A/G]TACTGCCACAGGAAT	78514
rs252110812	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77386308	AGGGAGATCTCTGTG[C/T]AGCCCTGGCTATCCT	78514
rs252139514	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77360642	CACAGATACATTTGA[G/T]AAATCAAATTAAGCA	78514
rs252142979	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77259973	GATCAAAGCTGCAAA[C/T]ACCATAAACTGAGAC	78514
rs252145121	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77342201	CACAAGAGATACGCC[C/T]CCATCACAGATCCTA	78514
rs252152829	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77427166	AACAGAAGCCACAAC[C/G]GGTCAACAGACCCCC	78514
rs252154315	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77289765	TGGTGACAGCAGCTA[C/T]GGGAGGGTGTTCATT	78514
rs252156741	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77514446	ACTTACTGTCACATC[A/G]TCTTTTTACTCTCTT	78514
rs252158232	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77364386	AGTTCCCAGCTCACC[-/T]TGGGGGCATGCTTGG	78514
rs252162694	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77452707	GAGCCACACACCCGT[-/C]CAGTCCAGTCATATT	78514
rs252175542	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77448717	CCTGTGCACACTGCC[A/G]CATCCCTGGCCCTGT	78514
rs252180940	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77331886	TTCGAGACCCCCATG[A/C]CTGTCCGTGAAGTCA	78514
rs252186207	snp	A/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77338302	CCTCCCTGAGTCACC[A/G/T]CTAGAATACCCGTAT	78514
rs252195684	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77513874	ATGCCTTATACTTTT[C/T]CCCCTAGAAAGCCCA	78514
rs252198880	in-del	-/TTAAGGGACA			intron-variant	Arhgap10	Mm_Celera	8:77278063	GTAAGAAAAGGGACG[-/TTAAGGGACA]TAAGCGGCTACCTTA	78514
rs252199368	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77431712	TGGGGAAGGCCAAGG[-/T]TTTTTTCTATCTGTG	78514
rs252206355	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77443290	TTATACCATTTATGG[C/T]ATAAATTCACATTCA	78514
rs252209934	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77418437	CTCAGGACAGGCTTA[A/T]TGTCCTATGATATAA	78514
rs252211955	in-del	-/CAATGGGCAC			intron-variant	Arhgap10	Mm_Celera	8:77343775	AATGTAAGTGCTGAG[-/CAATGGGCAC]TGGGCACAAACCCAC	78514
rs252231088	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77491329	AAAAAAAAAAAAAAA[A/C]ACCTTGCTGTGGAAG	78514
rs252235885	in-del	-/AAA			intron-variant	Arhgap10	Mm_Celera	8:77377229	AAGATGTTTTTTAAG[-/AAA]AAAAAAAAAAGAATT	78514
rs252247306	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77295141	TCACTTTCATCTCCA[A/G]CAGGCTTACAAACTT	78514
rs252249270	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77332593	AGAGTGTGATCTTTC[G/T]TTGAGACCTTGATAT	78514
rs252261907	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77414631	AAAATACAGAGCAAG[A/G]CTAGGTGGTGCGTAC	78514
rs252263060	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77448352	GACTATAACATTATA[C/G]AAACACTAGTTGAAC	78514
rs252263624	in-del	-/GACCAT			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485087	CTTCCCCTCAGCTTC[-/GACCAT]TACCAGTCACTCACT	78514
rs252270781	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77454754	CTTCATGACTTCATC[A/T]TGGTAGATGTATGTG	78514
rs252271876	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77297165	GCTGTTCTCAAGAGC[A/G]TTCATATTCACAAAC	78514
rs252290516	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77313588	AAAAGGTACAGTCAG[A/G]ACTTCCAGGTCCCTG	78514
rs252302189	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77333170	CCATATGAGTGCATG[C/T]TGCTAATAAAGGCCA	78514
rs252315908	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77318421	ATTTAACTTAAAATA[C/T]GTAGATCATGTATTG	78514
rs252322460	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77370787	CAGCCTCACTTCCCC[-/G]TCAGAGGACCAGTCG	78514
rs252325190	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77424114	CAAGATGTCTAATTA[A/G]AGTGATGTGGAGGTG	78514
rs252328133	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77263249	TCTCCCAGGAGAATT[C/T]CTGTTATTCCCACCC	78514
rs252330974	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77307272	GATACTCATCAGAGG[-/A]AAAAAATCTACCAAG	78514
rs252353867	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77297696	CCAGGAGTAGACGGC[C/T]AACACAAAGCACAGA	78514
rs252374621	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77447081	GGTTTGAGTGGTTGA[-/T]TTTTTTTGTTTGTTT	78514
rs252385547	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77467309	ATAAATTAATCATTA[A/T]CCTCTAGCATTTGCA	78514
rs252422384	in-del	-/TGTGTGTG			intron-variant	Arhgap10	GRCm38.p3	8:77406367	TGACTAAATACTAAT[-/TGTGTGTG]TGTGTGTGTGTGTGT	78514
rs252451341	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77398855	GCCTTTTAGAGAAAG[A/G]ACAATAAAATTCAAG	78514
rs252471709	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494443	AGACGATGGCCCAGG[C/T]CCTAGTTTATAATAC	78514
rs252472931	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77360589	TTTGATCAGTCCCTA[C/T]AACAGAACTCATTTG	78514
rs252484016	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77349891	TCTTCCAACTTCAAG[C/T]GTACTTAGGTACAAG	78514
rs252490637	in-del	-/GCGT			intron-variant	Arhgap10	Mm_Celera	8:77382037	TGTACATAAGCTCAA[-/GCGT]GCGCGCGCACGCACA	78514
rs252490829	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77409177	CATGACGAGAACATA[C/T]GCTCAGATGTGCGCA	78514
rs252501184	snp	A/G			upstream-variant-2KB, downstream-variant-500B	Arhgap10, 0610038B21Rik	Mm_Celera	8:77518722	ATGCGTTCTAAAGCA[A/G]AACTCAATACCTTCC	78514
rs252504725	in-del	-/G			intron-variant	Arhgap10	GRCm38.p3	8:77441540	ATACTATAATGAAAA[-/G]TATTATTACGCTTTA	78514
rs252506732	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77462356	GGGGGACTCCCATGA[A/G]AAGCACCATTAGTCA	78514
rs252511369	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77428132	TGGAAAAGAAGCAGG[C/T]TAAAGAAAGATAAAA	78514
rs252517694	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77269762	CAATGAATGCTTAAC[C/T]GTGACCATTAATGGA	78514
rs252524944	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77432856	AGCGTTAGGAAAAAA[A/G]CGGCGTCTCATTTTC	78514
rs252531000	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77409689	GACTGCAGGAAGGAT[C/T]TCAGCAGCGTCCAGG	78514
rs252532256	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493908	AGAGAGGTAGAGTAA[C/T]TTGAGCAAAGTAATA	78514
rs252543439	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77402207	TGTCATCTATTCTGC[A/C]AAACTCAAGTTTAGG	78514
rs252548055	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77404735	ATTGCCATTCAATAA[A/C]GACCTCAACAGGAAC	78514
rs252566959	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77427866	ACAATTATCCCTCCG[A/C]GTTTATTCTGTGAGT	78514
rs252567789	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77435532	GTGGCACCAGCAAAG[C/T]CTTTACCAGAAGAGA	78514
rs252578414	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77319854	CCCAGTCCAGGCACC[A/C]GATGTGGATATAGCA	78514
rs252583050	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77454973	TCTCGTTAAAGCCAT[-/G]GAACTTACGAAGCTA	78514
rs252583511	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77499936	CCTGGCTTTAAGCTG[C/G]TCTCTTAGCAACACA	78514
rs252586431	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77354052	AGTGCTGCTTTCATG[A/G]GAGAATAAAGACACC	78514
rs252587992	in-del	-/TATGTGGG			intron-variant	Arhgap10	Mm_Celera	8:77337846	CTCTGGCTCCTTCTC[-/TATGTGGG]TATGCTAGGTACCCA	78514
rs252598821	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77404948	AGAAACCTATTCTCA[A/C]TGGTTTCTGTAAGCA	78514
rs252602345	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77312721	CTCTGAACCAGGAAC[C/T]GGGGCCAAACATTGG	78514
rs252604509	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77439896	TACCAAGGACACTGG[A/G]CCCAGTAGCCTTGTT	78514
rs252636547	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77380399	GCTGGATGAAGAATC[C/T]GACGCCTATACACCG	78514
rs252643882	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77480691	GGAATCAGGCTCCCC[A/G]GAACTGGAATGACAC	78514
rs252647600	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77382878	AATTAAGGTAATGTA[A/G]CTTTTGTTTCACTGT	78514
rs252659885	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77380953	ATCTGGGGAGTTAAT[A/G]TCAGTAAGTTTCTAG	78514
rs252666368	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77470441	TTCTGCACACACTAT[-/C]TAACTATCGACAGCT	78514
rs252676209	in-del	-/TT			intron-variant	Arhgap10	Mm_Celera	8:77293956	CATAACACCTTGGTA[-/TT]TCTTTCCATGGCCTC	78514
rs252679490	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77475551	TGAACTCCATGGATA[C/T]CACATACATACGTGG	78514
rs252686817	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77282106	AGAGACTCGCAGTTC[C/T]ACTAAAACTGAGATA	78514
rs252687808	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77428721	AAGCCCAAAGATCTT[C/T]TAGATTTCAAAACAA	78514
rs252700759	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77381467	GACGGTAGCTCGTAT[C/T]ACGTCGATGAGACAC	78514
rs252717393	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77486590	TCTCATTTATTAGGT[C/T]AAAGTGGTAGTGCAC	78514
rs252723587	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77475026	CTAACTACTAGCCTC[C/T]AAAGTCTGGTTGCCT	78514
rs252728350	in-del	-/TCCTCGGTCAGA			intron-variant	Arhgap10	Mm_Celera	8:77316859	GCCCAGCACTGCATT[-/TCCTCGGTCAGA]TGAAAGTGCTTCTCC	78514
rs252735574	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77488166	AGGGAAGAGAAGCTC[A/C]TGACTGTAAAGGATG	78514
rs252735817	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77403853	CAGGCTGGGTGGACG[-/C]CCACTGCTCACTACG	78514
rs252747456	in-del	-/GGA			intron-variant, cds-indel	Arhgap10	Mm_Celera	8:77493130	AAACAAAAAATTAGT[-/GGA]GGACTGAGAAAAAGA	78514
rs252748277	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77283245	TTAATTTACACAAAC[C/T]TCACAGTGGCACATC	78514
rs252749059	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77471705	GATGTTTATTGTATA[A/C]TATTGCCTTATCATG	78514
rs252749787	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77274305	TAATTTAATTTTTTC[A/T]TTTTTTACTTATTTA	78514
rs252750322	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77268915	CCAGATGGATCAAGG[C/G]TGTCGCCCCACAGGT	78514
rs252760394	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77474504	TGTGTCATACGTACA[C/T]ACATTGTGTCACAAA	78514
rs252764098	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77397938	TCTAAGCTTCCTGAC[G/T]GTGGATGTGACCAGC	78514
rs252764366	snp	A/C/T			intron-variant	Arhgap10	GRCm38.p3	8:77405993	GCACAATACCCCCCC[A/C/T]CCCCACAGTGCACTG	78514
rs252765598	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77480900	ATTGTGAAAAGAGGA[A/C]GTGGTTTGCATACCT	78514
rs252767481	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77377311	GCCCATCAAGAAAAA[C/T]AAATGTACTGGGCAT	78514
rs252768579	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77438389	GGCCTGCCAGATACA[C/T]CTCACACATTCATTG	78514
rs252773777	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77438695	CTCACTGCGGCTCGG[-/C]CCCTAACTGCTTCTC	78514
rs252774796	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77274958	GAAGATGGCCTAGTC[A/G]GCCATCAGTGGAAAG	78514
rs252784648	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77374927	TGGTCCCTACTTCAA[C/G]AGCCTTTTTTCCTCT	78514
rs252784790	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77370039	AACCAGCAAAGACTG[-/T]GAGTGGCTGTGCACT	78514
rs252789777	in-del	-/CACACACACACACACACACACACACACA			intron-variant	Arhgap10	Mm_Celera	8:77268542	GCGTGAGTTAGACAT[-/CACACACACACACACACACACACACACA]CACACACACACACAC	78514
rs252792659	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77273720	ACCTGTTATAGACAC[A/G]CTGAAATACCTACTG	78514
rs252797361	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77501838	GCTATCGTTTGGATC[A/G]TAAATGCCCCCCAAG	78514
rs252798902	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77479546	AGCACTGGGTCCAAG[A/G]AGGTCAGAGGTGTGA	78514
rs252801539	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77347904	AAGCGCCTCTTCCCA[A/G]GAGCCTACGACAGTT	78514
rs252802134	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77414809	TATTATATATAAATA[C/T]ATATACATGTACACA	78514
rs252807426	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77263760	GAGGACCCGGAGTCC[A/T]CTCCAATACTTCACA	78514
rs252807821	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77255839	TCCTCCCAGTGACAA[A/C]TGGAGAGTGAACATT	78514
rs252810389	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77295269	GCTGCTTCAGTTACC[A/C]TAGTTCTCCTTCTGA	78514
rs252823989	in-del	-/CAATGTCACACTGGAAC			intron-variant	Arhgap10	Mm_Celera	8:77367437	CACCCCATTCTCTCT[-/CAATGTCACACTGGAAC]CAGGAGGGCAGAACT	78514
rs252825669	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77408809	TCAGGGAATTTACTC[A/G]TGGGCCTTTCCCTCT	78514
rs252827683	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77288378	GTGACTCCAGACTGG[A/G]TTGCTGCAGCTTGCG	78514
rs252831188	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77269009	ACAGCTGGGTCTTAA[C/T]AATCTTGGTGGTAAA	78514
rs252832255	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77516287	TCATCAAAAAAGTGA[C/T]TTCCAGTCCCAACTT	78514
rs252833502	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77274070	GTGAGCTGCTTTTTC[C/T]TTCTGGGATGTCAGG	78514
rs252833991	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77444894	CACTGACCTCTCCAG[A/G]ACCCCCACTGCCTCT	78514
rs252836419	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77500967	ATGAATGGACTGGGG[A/G]ATATGTGATTTGTAT	78514
rs252840152	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77333082	ACGGACAAAATCTAA[C/T]GAGACCAGGGTGACC	78514
rs252864212	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77256515	TGAAACAATTTGCTT[G/T]CTATATAACAACCCT	78514
rs252864235	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77447074	GGGGGGAGGGTTTGA[-/G]TGGTTGATTTTTTTG	78514
rs252866272	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77323986	AAAAGACTCCCTCCA[-/C]CCCCCCCCATCCCCT	78514
rs252867029	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77340716	GCTGTCCTGAGAGCC[A/T]CTAGTGTCACGCACA	78514
rs252869179	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77277475	TTGTTTGAAAAAAAA[A/T]CAAAACAAAACAAAG	78514
rs252878235	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77500729	TGGATTCAGGGAGCA[G/T]ATTCAGGTCACCAGG	78514
rs252887166	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77386371	TCGGATACTAACTCC[A/G]CCTCCCAAGTGCCAG	78514
rs252899099	snp	G/T			utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250517	GGCCCGGGGAGGGGG[G/T]GGGGAGGGGGAGGAG	78514
rs252899390	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77477404	CCCTGGTCAGCACGA[C/T]CGAAGACTCCCCCAT	78514
rs252907583	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77288295	AACATATTGGCTGGT[C/T]TCAGATTACTGGGTG	78514
rs252913706	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77353436	TGAAGAACTTCACAA[A/C]GCGTAATCTTTTTTC	78514
rs252919026	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77368854	TTGCTTTCTGTTCTT[G/T]TTTTTATTTTTTAAC	78514
rs252949933	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77456037	TTAAGTAGAGAAATT[G/T]CACCTAGAAGCTTGC	78514
rs252953927	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77462681	TGTTCTCTTCACCCC[A/G]AGCCACCCCTCTCTA	78514
rs252958452	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77369436	TTCTGTTCTATTTTC[A/G]TGGTAGCTTGTATAC	78514
rs252986159	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77259850	AATAATAATAATAAT[-/A]AATAAATCTTTAAAA	78514
rs252986470	in-del	-/AAAA			intron-variant	Arhgap10	Mm_Celera	8:77418938	AACCCCTGGTCTAAG[-/AAAA]AAAAAAAAGGTTAAT	78514
rs252988768	in-del	-/CTCTG			intron-variant	Arhgap10	Mm_Celera	8:77499012	CCCGCTGCCCGCTGC[-/CTCTG]CCGCTGCCTCTGCCT	78514
rs252996380	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77362616	AAGCATTTGGCAGGT[A/T]CGTGCCCTGCCTCCT	78514
rs253003548	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77505480	TTACTTGTTTAAGAG[G/T]AATAACTGTGGTGCC	78514
rs253008840	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77323029	CCTCCCGACTGGTTC[A/G]TTCAGAAGCTGCAAG	78514
rs253013596	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77450528	CCAGGACCTTGACCA[A/G]GAACTCATCACATAA	78514
rs253017109	in-del	-/CA			intron-variant	Arhgap10	Mm_Celera	8:77446093	TTTTTTTTTTCCTTC[-/CA]CAGATTTTAATTTTC	78514
rs253021114	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77379759	CAACCCATGGTCTGT[C/T]ACACACCAAGGTTCT	78514
rs253025680	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77251635	GTCGCATGACAAGGC[C/T]CAGACTGGACAGCAA	78514
rs253026698	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77266942	ATCCTTGTGAAGAAA[A/G]AGCCGCCACAGACAA	78514
rs253029119	in-del	-/TGAGCACCC			intron-variant	Arhgap10	Mm_Celera	8:77497171	GCTGGAGTGTATGTA[-/TGAGCACCC]TGTGTGTGCCTGCTG	78514
rs253037896	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77476288	TGTGATAAAAGTATT[-/A]AAAAATGCATAACAA	78514
rs253039931	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77363080	GAATGACGTCCTAAC[A/G]TGCCTGTGTCCGGAC	78514
rs253045113	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77263371	TGACAGGAAACAAAG[C/T]TGGAGTACATCTTAT	78514
rs253069778	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77271909	TTCACTGGCAATGAA[G/T]TCACCTGTCTGTCAC	78514
rs253077041	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77450245	AGGCCCTCGGAGCAC[A/G]CTTAATGGAGAAGTG	78514
rs253086727	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77512216	ATAAAGACCCATGGA[C/G]GGCAGCTCACTGAGC	78514
rs253110168	in-del	-/CCACCCCCCCCCA			intron-variant	Arhgap10	GRCm38.p3	8:77506070	TTGAACTTGTGACCA[-/CCACCCCCCCCCA]CCCCCCCCCCCGCCT	78514
rs253111530	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77254616	TGTTTGTGATTATTC[C/T]AAAACCCTAACTAGG	78514
rs253118345	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77261333	GGCCCTCTCTGCTCT[A/C]TGCCACACTGCTAAC	78514
rs253120960	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77468406	ACCCATTGGGGTAGA[A/G]CCCTGTTGGAGTACA	78514
rs253135084	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77498058	CAAAATGAATAAAGC[A/G]GAGAAAGCAAGAGAA	78514
rs253136468	in-del	-/TGAG			intron-variant	Arhgap10	Mm_Celera	8:77416237	AGCCTGATGCAGTTC[-/TGAG]TGAGCTCCGTGCTCT	78514
rs253138561	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77361455	TTATCACCTCGGATC[A/G]TTTCCAGTTGCTGAG	78514
rs253142003	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77290220	ATAACAAAACAAAAC[-/A]AAACAAACAAAAAAA	78514
rs253177775	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77474301	GAGAAGCATCCAACA[C/T]GGATCAGAGAAGCAT	78514
rs253179569	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77467828	CATCAGAGCTGAGAA[C/G]TTTCTCACAGCAAGC	78514
rs253180057	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77335750	GCAGAAGTAGGAGGA[C/T]CCAGATGCAAATAAA	78514
rs253189103	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77442217	CCCCTCCCTCCCCAT[-/C]CCCCCCACACCCCAT	78514
rs253189132	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77305626	TGCACAGAGTCATCA[A/G]GACACAGGATCCAAG	78514
rs253192874	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77354835	CTATGAACCCATCCC[A/G]TCTTCCACACTTAAA	78514
rs253192963	in-del	-/GAG			intron-variant	Arhgap10	Mm_Celera	8:77463029	ACACAAGAGAGAGGT[-/GAG]GAGTCTGCTTGAGTG	78514
rs253194248	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77362111	AGGTTAGCGAGCCTG[A/G]GGAGAGGATTCGGAA	78514
rs253222637	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77317144	CATCCTAGAAATCGG[C/T]CCTGGACTCAGTACA	78514
rs253236008	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77473816	TTTATCCTTTTAAAC[A/G]ACAAGACAGTAATCA	78514
rs253250165	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77355615	GTTGCATAATGATTT[C/T]CTGTATGCAGTGGCT	78514
rs253250886	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77373460	TAACCACAGACCTGG[A/G]CTAACGCACCACAGA	78514
rs253253330	in-del	-/AGG			intron-variant	Arhgap10	Mm_Celera	8:77483393	AGGAGAAGGACTGAG[-/AGG]AGAAGGGCAGAATAT	78514
rs253275040	in-del	-/T			intron-variant	Arhgap10	GRCm38.p3	8:77457648	TAACAATAATAATAA[-/T]AACTAACATACCACT	78514
rs253278432	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77423601	CAGCTCTGGTGCTTT[A/C]AAGGTTTATGATAAA	78514
rs253280429	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77430224	ATGAGTCAGTACAGT[C/T]TAGGGTGTCCGACTG	78514
rs253289233	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77368459	CCACCAACACCCTTA[-/C]CCTTTTCACTGGTGC	78514
rs253306736	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77333966	TCAGAGCAGAGATCA[A/G]CATCCTGGGAAACCA	78514
rs253310956	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77373059	CCGATCTCTCTGTAA[C/T]GGTCTTTTTTTTGGG	78514
rs253317290	snp	A/C			upstream-variant-2KB, downstream-variant-500B	Arhgap10, 0610038B21Rik	Mm_Celera	8:77518973	GTGAGCTGTAGGAGG[A/C]GTCTTAACCCTCTGG	78514
rs253320311	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77457351	CCCAATGGAGGAGCT[A/G]AAGGAAGTACCCAGG	78514
rs253320521	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77253389	CCTCTCCAGCGCTGG[A/G]ATGGTGTGAAGTGCT	78514
rs253336823	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77429608	CCAGATCCCTATAAT[C/T]CTGGCAACTGAGGGA	78514
rs253339946	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77328568	TCTCTCCTCTTCTTC[A/G]GACCAGTACTTTTTC	78514
rs253357285	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77417970	AAGAAGCCTCAGAGA[C/G]CAGAATAAAACTGAG	78514
rs253368040	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77334414	GTTGGGAAGGAGAGT[A/G]GAGCAGCGCGGAGAG	78514
rs253369811	in-del	-/CAGATC			intron-variant	Arhgap10	GRCm38.p3	8:77400735	CAACTGTGGCTCCTT[-/CAGATC]CCACGCCTAGGCCAT	78514
rs253372842	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77367704	TCCTAAGGATTTTAG[C/G]CCCCCCCTCCCCCCT	78514
rs253377274	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77340498	CAGATCTCTCAGAAC[C/T]GAGTTCCCCCACGGT	78514
rs253391294	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77402005	AACCCCCAACTACCA[C/T]CCACTCTTACCCCAA	78514
rs253401047	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77431038	AGCACACTAACCAAA[A/G]GAACACAAGCGTGTG	78514
rs253402602	snp	A/G			utr-variant-5-prime, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77517860	CTAGCAGGGCTGAGC[A/G]CGCGGCGAGCGCAGC	78514
rs253421728	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77353995	AACACCAAAGAAGCA[C/T]GGGAAATTTAGAAGG	78514
rs253423674	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77411825	CTGTATGTGCTACAA[C/T]ACCCAAGAGCTCCTC	78514
rs253424635	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77328752	GACATCTCCTTCCAT[A/G]CCGCCCCATGTATGA	78514
rs253451978	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77308395	AAAGAGCCCAGGACC[A/T]GATGGGTTTAGTATA	78514
rs253453691	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77396419	CAGAGAGATGAATCA[A/C]TAGCAACAGCAAACG	78514
rs253455779	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77417673	CAAGAGAATAAGATG[A/G]AAAAAAAAAGAGAGA	78514
rs253456804	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77430422	GCCAACACTGCCCAG[A/G]AAAAAGAAACGGCGT	78514
rs253460321	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77438587	ATTGAGAAATCATTC[C/T]ATCTTCACCTCAGCA	78514
rs253467101	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77316347	ATAGCATTCTTTTTT[C/G]TTTCTACAGTTTAGG	78514
rs253471994	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77322338	AGGAAGGAGCTTGGT[A/C]ATGTCACACCTCGAT	78514
rs253479943	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77417867	GCAACACACACATGC[A/G]AGCGTGCACACGTGA	78514
rs253490005	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77346253	GATGAGGGAGAGCTG[A/G]TGGGGAAGGAACACT	78514
rs253503306	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77455486	TCTCAACTTCTGGAG[C/G]CCCTGTAAGATAAGT	78514
rs253513781	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77438002	CTGTGTGCAGCCATG[C/T]AGTGAGATATATACT	78514
rs253516940	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77293609	CAATATAGGTGGAAG[A/T]AATCTGGTGGGGCCT	78514
rs253525880	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77504288	GGGGGGGGGGGGGGA[A/G]CAAAACAAAACCTTC	78514
rs253526980	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77323110	ACACTTAACTCATGA[G/T]CGAGAAAATGTGGAA	78514
rs253530155	in-del	-/CT			intron-variant	Arhgap10	Mm_Celera	8:77461837	ATTCATACCAAAACA[-/CT]CTGTTATAAATTCTG	78514
rs253530895	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77423957	GTCCTGGGCAGGTGT[A/G]CATTGCATGGCCCTA	78514
rs253531538	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77309012	ATATAATTTTATTCC[A/G]AAGAATAGTAGAATG	78514
rs253544836	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77376498	GTGCTGCAGGCATCT[-/C]GGCAGCTCTCCAGCT	78514
rs253555465	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77286384	AGGAAGTCTTCAATA[C/T]TGTCTTAATCACCAT	78514
rs253561533	snp	A/G			intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77502154	CAGAAAGCTAACACC[A/G]AGAACGCCTCCTGCT	78514
rs253566997	snp	A/C			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77502770	GTGGGACAAGTGGTG[A/C]GTTATCAACCAACCA	78514
rs253575733	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77447884	TCCACCGTCAGCAGA[A/G]GTGACTGTGTGTCAT	78514
rs253577071	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77415636	TTATGTTAATTATAA[A/C]TTAGGGTAGAAATTT	78514
rs253582650	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77285449	TAAAAACATCTTCGG[A/G]CATTAAAAATCCCTA	78514
rs253587061	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77424163	AAAAATCCTCTCTGA[A/G]GTAATTGAAAGTGAG	78514
rs253603970	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77489574	GTTTACCCACCCAAA[A/T]AAGCTCTGTAACTTC	78514
rs253607447	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77271866	ACCTATGATGTCACG[A/T]ACTCCGAGGAGCCTG	78514
rs253619781	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77508616	CTGCTACCCAAGTGC[C/T]TGCAACTCCTCACCT	78514
rs253626264	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77455478	ACTTCTACTCTCAAC[-/T]TCTGGAGCCCCTGTA	78514
rs253631454	snp	G/T			intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77502166	ACCGAGAACGCCTCC[G/T]GCTGAAGAAGCAGCA	78514
rs253642063	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77410260	TGCTTTAAGGTTTTT[G/T]GTTTGTTTCTGGACA	78514
rs253642712	in-del	-/AA			intron-variant	Arhgap10	GRCm38.p3	8:77445302	GAGAAAGAAAGAAAG[-/AA]AGAAAGAAAGAAAGA	78514
rs253645699	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77497378	AAAAAAACGTCTGCA[C/T]CCACAGATACTAAGG	78514
rs253649228	in-del	-/AAA			intron-variant	Arhgap10	Mm_Celera	8:77386229	ATCATCCGGGTTATT[-/AAA]AAAAGGGATTAAAGG	78514
rs253655109	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77321192	GCCTTCTTTTAGTTG[C/T]TTTTGTTGGGTGCAA	78514
rs253666389	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77411206	TTACTGCCCTGCTCA[A/G]CCAGGGAAAGCATAG	78514
rs253669190	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77410738	GACAGCATGCAAACA[C/T]GCCAGATCTTCTATG	78514
rs253684232	snp	A/C/G			intron-variant	Arhgap10	Mm_Celera	8:77507800	GGAACTCTACCTCTC[A/C/G]TGTCCAGTCTTCTCT	78514
rs253688646	in-del	-/CG			intron-variant	Arhgap10	Mm_Celera	8:77341583	AGTGCTCTGTACTCA[-/CG]GGCAGGCACTGTCCT	78514
rs253696008	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77265904	CCCTAACATTTCATG[A/T]CACATGCTGCAAGAC	78514
rs253699631	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77281273	GGTTTCACAGCCTAA[-/C]CCTTGACTGCCACCC	78514
rs253705527	snp	G/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503027	CCACTTACAAGCAGG[G/T]GGAATGGAATGCCTT	78514
rs253706892	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77497123	TTTTTCATGAGTGTG[A/G]TTTTTTTTATATTTA	78514
rs253721034	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77321164	GCTGGACCGTGTCAG[A/C]TAAAGGAAACCCGCC	78514
rs253723561	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77406727	GGGCGGTGGAGAAAA[A/T]GGTTCACTGATAGTA	78514
rs253725935	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77411426	CACACATGCATACAC[A/G]TGTACACATGTGTAC	78514
rs253729899	in-del	-/GGATGGTCTCCTCACCGAGGACCCT			intron-variant	Arhgap10	Mm_Celera	8:77507288	ATAATCAGGATAGCC[-/GGATGGTCTCCTCACCGAGGACCCT]GCTCCCCACACACTC	78514
rs253736666	in-del	-/CA			intron-variant	Arhgap10	Mm_Celera	8:77376603	CTCAGCAGCTCCTCC[-/CA]CACGAGACTGTCCTC	78514
rs253752212	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77291170	AATGCATCAAGGGGA[A/G]TCAGGGACTTCAGTC	78514
rs253765825	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77375841	AACATTCAAGCTGAG[A/C]CGCTAGTGAGGCCCC	78514
rs253769729	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77388912	CACATTATTGTACAG[C/T]CACCCCAATGATTCA	78514
rs253776096	in-del	-/CC			intron-variant	Arhgap10	Mm_Celera	8:77338790	GATCTCTATTTCTAA[-/CC]AAGAAAAATGTAACT	78514
rs253776408	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77443350	CAGTCACGGGGAAGC[C/T]CACAGTTAAAGAGTA	78514
rs253777039	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77315998	CACACCTCTTCGGGA[C/T]AGATTCTGCAAGTGC	78514
rs253777287	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77407186	AAAAATAAACAGGGG[C/T]TGTAGAAATGACTCA	78514
rs253797382	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77405917	AAAATGCTGGGTCCC[A/G]TCAACAAAATATACT	78514
rs253807310	in-del	-/G			utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250518	GCCCGGGGAGGGGGT[-/G]GGGAGGGGGAGGAGA	78514
rs253824041	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77382464	TGGGCCATCCACTCT[A/G]TGGTATTTTCTGTGA	78514
rs253828817	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77291743	AACTCACCTCCTCTG[C/T]ATCCCAATTTCTTTA	78514
rs253831228	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77284460	GCATGCTTGAGATCA[A/C]GGCACCCTCCTTCCT	78514
rs253842386	in-del	-/CCTCG			intron-variant	Arhgap10	Mm_Celera	8:77428088	ATAAAATCTAGAGAC[-/CCTCG]CCTCGGCTCTCCATG	78514
rs253844010	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77501065	TTTATAGAATGATAG[-/A]AAAAAAATTAATAAA	78514
rs253858701	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77284630	TGAGAATGTTAGGAG[A/G]GAGAGCCTAGCTGGA	78514
rs253859750	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77292640	AGAAAGAACACGCTC[C/T]GGGGGAGACGCGCTT	78514
rs253865045	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77285251	TACGCGTGTGCGTGC[A/G]TGCGTGCGTGTGTGT	78514
rs253871867	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77358961	GAGTAGTCTGTGAGG[A/G]ACACTATCACCATTG	78514
rs253875818	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77416414	CCTTGGTCATCATAA[A/T]AGAACTAAGACGCCC	78514
rs253893063	in-del	-/GT			intron-variant	Arhgap10	GRCm38.p3	8:77387210	TGTATCTGTGTGAGA[-/GT]GTGTGTGTGTGTGTG	78514
rs253914882	in-del	-/CATCAT			intron-variant	Arhgap10	Mm_Celera	8:77441310	GCGAAGTCCACAACC[-/CATCAT]TCTCCCTCTCCCTGC	78514
rs253939497	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77488618	TGTGCCCAATACATG[C/T]AAAGTGCTAGGCTAT	78514
rs253940506	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77276772	GGCAAGAAGCTATGA[C/T]GTCAAACAGAATGTG	78514
rs253942368	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77377553	ATTTTATAACCAGTA[A/G]TTTGTCAACTTGCCA	78514
rs253958156	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77297588	TCTGCTAAGAGAACA[C/T]AGCAATAAAGTGACT	78514
rs253971898	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77410584	TCACATTCACAGGGA[A/G]TGACCTTATGAAAAC	78514
rs253979241	in-del	-/AATAT			intron-variant	Arhgap10	Mm_Celera	8:77434465	AAAATAGTTCATAGA[-/AATAT]AATATATAACACCTG	78514
rs253979315	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77252453	CTATTCTTAAAGGTT[C/T]TATCCATACATTGTA	78514
rs253982635	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77277726	TATTGCTGCCACCAC[C/T]ACCCCCAAGCCTAAA	78514
rs253982751	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77264905	GGAGGCTGTACCTCC[A/G]GCATGCTAACAGGTT	78514
rs254015098	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77257776	GGAGGGAGTTTCCCA[A/G]GGAGCCCACATATGA	78514
rs254015893	in-del	-/AAA			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493306	GAGGAGGAGGAAGAG[-/AAA]GAGGAGGAGAAGGGG	78514
rs254016762	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77440699	ACTTCCAGAAACTCC[A/G]GTTTCGGAGGACCCA	78514
rs254023467	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77458557	AAATCATACAGCCAG[A/G]GGAAGTGACAGGCAT	78514
rs254028833	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77257998	ACACAAGCTGGAGTT[A/C]TCACAGAGAAAGGAG	78514
rs254036825	in-del	-/GCGCGCGC			intron-variant	Arhgap10	Mm_Celera	8:77274196	ATGATTGGTGTGTGT[-/GCGCGCGC]GTGTGTGTGTGTGTG	78514
rs254045598	in-del	-/GCGCGTGC			intron-variant	Arhgap10	Mm_Celera	8:77417884	CGTGCACACGTGAGG[-/GCGCGTGC]GCACACGCACACACA	78514
rs254056064	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77447827	ATCATCATGGTAGCG[A/T]GCAGCCAGACCGGTA	78514
rs254056193	snp	A/G/T			intron-variant	Arhgap10	Mm_Celera	8:77381811	GCCCGAAAAGATCAC[A/G/T]TTTAATGGCATTCCA	78514
rs254056264	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77483631	TGGAAACCCTTCCTT[C/T]GTTCCCCAAAGGTGG	78514
rs254066792	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77400689	CTTAACTGCTGCGCC[A/G]TCTCTTCAGCCCCGT	78514
rs254074603	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77388605	ACATGGGGATGAAGC[A/G]AGCCAGCTGAGTGTA	78514
rs254079032	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77458111	GAGCTCATAAATCTG[C/T]TTGGACAACTGGAAA	78514
rs254083552	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77447085	TTGAGTGGTTGATTT[G/T]TTTGTTTGTTTGTTT	78514
rs254084125	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77463946	CTATTACAAAGAACC[A/T]TCCAATTTAACCAAA	78514
rs254085315	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77337335	TTATTCCCAATCCTG[A/T]CTTGGGCGGTGCTGA	78514
rs254096087	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77258157	GCTAAGGGAAGCAAG[C/G]CAGTAAGCAGCATTC	78514
rs254114388	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77488111	TCAATACAGACAAGC[G/T]CATAGACCCAGAATC	78514
rs254114674	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77253091	AATCAATGTGGGAAT[A/G]CAGAGACTAGAACCC	78514
rs254119184	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77452890	AGAGCCTCCTACAAC[C/T]CACCCACACATAATC	78514
rs254125518	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77291923	GCCATTACAGTCTTT[C/T]TCCTCACTCTGTGCC	78514
rs254128652	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77421929	TATGATTCCCTCTCC[A/G]GATTCCCGAGCTCAC	78514
rs254136940	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77453240	TTTTTCTTTTAACAT[A/G]TAAGAATGTTCCTGT	78514
rs254141701	in-del	-/TTCATCTC			intron-variant	Arhgap10	Mm_Celera	8:77410531	TGCTTGGCTCTGCTA[-/TTCATCTC]TTCATCTCGTTGGCT	78514
rs254146077	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77375797	CTTCACAGACAGTGA[A/G]AGGAAGATGAAAACA	78514
rs254149993	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77253426	CATGCTTTTGCTGTC[C/T]AACTCTTTACCATCT	78514
rs254161174	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77421426	GGGCTTCTGCTTGGC[G/T]AGGCACAAAGGTCTG	78514
rs254162208	in-del	-/AG			intron-variant	Arhgap10	Mm_Celera	8:77351679	GAAGACTCCTGGAAA[-/AG]AAAAAAAGAAAAAAA	78514
rs254173663	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77370293	GTGTCTACAGGATCA[A/C]GCTCGCATACAGAGC	78514
rs254179084	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77452541	CAGACGTGGTGGCGC[A/G]TGCCTGTATCCCCAG	78514
rs254196710	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77482572	ATGGCTTCAGCATCT[C/T]ACCCCTCTGCACTTC	78514
rs254197822	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77464377	CACCATCGTAATTAC[A/C]GTGTGGACATTCTTT	78514
rs254212355	in-del	-/GAGGAG			intron-variant	Arhgap10	GRCm38.p3	8:77363421	GAAGAAGAAGCAGAA[-/GAGGAG]GAGGAGGAGGAGGAG	78514
rs254220611	in-del	-/CC			intron-variant	Arhgap10	Mm_Celera	8:77341902	GGAAAAAAAATAAAA[-/CC]ATAAAAAATACGAAC	78514
rs254224252	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77404927	TGTGCCACCAAGCCT[A/G]GCTGCAGAAACCTAT	78514
rs254236890	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77370923	AGAGGTGGGACTTCC[A/G]ATGCAGGGAAGGAGA	78514
rs254237535	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77471324	ACACAGAAGTGGATG[A/C]TCACAGTCAGCTATT	78514
rs254238767	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77363609	ACTCAGGTCTTTATG[C/G]TTGGTCTGCAAACAC	78514
rs254242413	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77270080	AAGGACAGAGAGAAA[A/G]GACAAAGATTTCTGT	78514
rs254252248	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77489135	TGTCTCAATCTATCG[A/G]TCAATCAATCAATCA	78514
rs254253260	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77481943	TAGGGATGAGCGCAC[A/G]GCTTTTCAAGCACAT	78514
rs254257313	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77470645	CAGCCTTTCTAGTGA[C/T]TCTGTACTTAGGACC	78514
rs254257716	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77404914	GGGATTAAAGGCGTG[C/T]GCCACCAAGCCTGGC	78514
rs254268558	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77264442	GAGAGTAAATACCAT[C/T]ACCCTCCGATGAAGG	78514
rs254282619	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77440344	AAGGGCTCATGCTAA[C/T]GTGGTCCCTTAGATG	78514
rs254283392	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77399682	ACCACTACCTACAAG[A/G]CCCAGTGGCCCTTGA	78514
rs254286332	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77265001	TGGTCCCCAGAAAAC[A/G]CCACAGAATTTCTTC	78514
rs254290167	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77357316	CCGAGCGGCACAGCG[A/G]GCCACAAGGGGTCGC	78514
rs254316548	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77351053	GCTGGCACAAACACA[C/T]ACTCCAGTGGGTACG	78514
rs254317156	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77313316	ATCTGCTTAAGCACT[C/G]TCTTCACAAGGCAGG	78514
rs254323239	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77476781	TTGACTCTCCAAAGA[A/G]TCACCTTTGCACCAG	78514
rs254325520	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77452424	ACTCACAGAGATCCG[C/T]CTGCCTCTGCCTCCC	78514
rs254332588	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77380704	CAAAACAAAAAAAAA[A/C]CCTCAAAGCCCTGTG	78514
rs254339407	in-del	-/AGAAAA			intron-variant	Arhgap10	Mm_Celera	8:77434210	ACTATGTTGTATCTC[-/AGAAAA]CAGACACCAAAGGCT	78514
rs254340332	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77342091	GATGACCAAACCCTC[A/T]CCAAAGAAGCCCTCT	78514
rs254340381	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77350717	GTGCAATTTCAGCTA[C/T]TGCCAGTGCATAATC	78514
rs254344885	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77439717	AAAGTTGGCTAAAAG[C/G]GAGAGGAACAAAGCA	78514
rs254353308	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77426310	AAAAGGGCAAATCCA[C/T]AAGAACCTGTCAGGA	78514
rs254353912	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77364876	CTCTACTGTGAGAGG[C/T]ATGTACCTATGAGCT	78514
rs254356837	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77357633	CCTTTACCAAAGATA[A/G]GAAACAACAACGCTT	78514
rs254367300	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494943	GCATTTGTGAGCAAG[A/G]GAAGGGAATCCTTGA	78514
rs254370757	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77257088	GTCTTCAAGTGCTAC[C/T]GGCTCGGTGCCACCA	78514
rs254397367	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77469176	AGTGTCCAGCCCCAA[C/G]ACCCCAGTAATGGAA	78514
rs254399417	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77476248	TTCCATAAAGCTTTA[A/G]AATATTTATTTCTTA	78514
rs254404471	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77374830	GGTTCACATGCAGAC[A/G]GACAGTTGTCCCTAC	78514
rs254411532	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77342810	CACCCCCAGATGCTA[A/C]CAAAAAAGTAAGACT	78514
rs254416632	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77446452	ATGTGGTTAAACTGC[A/G]CTGGCCTTGCAACCT	78514
rs254430256	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77330738	ACTGACTACACAACA[A/G]AGTACAAGAGGAGAC	78514
rs254431722	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77513078	AAACCTCAGGCAGGC[C/T]AAGCAAGCACTCTAC	78514
rs254431969	snp	A/T			intron-variant, downstream-variant-500B	Arhgap10	Mm_Celera	8:77358498	ATCAGTAAGTGTCAA[A/T]ATGACTCCTGCCACT	78514
rs254434563	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77257691	TCCTTTCCCACTGCT[C/G]AGCATTGTGGGATAC	78514
rs254449956	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77434086	TTTGAATTTTAAATC[C/T]GAATGCTCTACATTT	78514
rs254466637	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77445798	TACTGGGAGAGCTCG[G/T]CCCAGAGCTGCCCAC	78514
rs254495066	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77434421	ACATCTATGTGCCCC[C/T]CCAACATACATACAA	78514
rs254496034	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77324298	GCTTCACAGTAAACG[A/T]GCTAAAAAGGTCACA	78514
rs254500951	in-del	-/CAT			intron-variant	Arhgap10	Mm_Celera	8:77488053	TGACAGCTGCAAGGG[-/CAT]CATCCTCAGCACACT	78514
rs254509953	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77463472	CTAGAGACACTCTGG[A/G]ACTAGAGACTGAGAT	78514
rs254518277	in-del	-/CGCACATGCATGCG			intron-variant	Arhgap10	Mm_Celera	8:77340904	ACACGCATGCATGCA[-/CGCACATGCATGCG]CGTACACACACACCA	78514
rs254527667	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77475864	GCTCATACATAACAA[C/T]TGGTGAAAAATTCAG	78514
rs254538296	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77269652	GCTTTTGAGAGCTAC[C/T]ACTACTACCCTTGCC	78514
rs254558914	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77273967	CAGCCCTAGCACAAA[C/T]TTTTAATCCAAGAGC	78514
rs254559027	in-del	-/CGAGTGAGCACACG			intron-variant	Arhgap10	GRCm38.p3	8:77489298	GTGTGCGCGCGTGCA[-/CGAGTGAGCACACG]CATGAGCGTGCATGT	78514
rs254563746	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77311760	AACCACAGGCAACCG[A/G]CACGCTCCTCAGGTG	78514
rs254564030	in-del	-/GGG			intron-variant	Arhgap10	Mm_Celera	8:77381973	AACATTAAAAAAAAA[-/GGG]GGGGGGGGCCTTTAA	78514
rs254570874	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77420467	GGGTCACGGTATGGC[-/G]GGGGGGCTGTGCCCC	78514
rs254576845	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77495089	TAAAGATCAGAACTA[C/T]GTATGTTGAAAACCT	78514
rs254600684	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77296127	TCAGAGGAGGATGTA[C/G]AACTTTTAGCTCCTC	78514
rs254621431	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77251570	GAAGGCAGGCCTGGG[A/C]CTTACCTACTACCTG	78514
rs254637560	in-del	-/TGTTGTTGTTGTTGT			intron-variant	Arhgap10	Mm_Celera	8:77347381	CTTTGTTTCATTTTC[-/TGTTGTTGTTGTTGT]TGTTGTTGTTGTTGT	78514
rs254649210	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77349577	GCCAGGAGAGCTGTG[A/T]TGTGTCCAGGGGAAA	78514
rs254655216	in-del	-/ACAGTGAGAT			intron-variant	Arhgap10	Mm_Celera	8:77324199	CTGTTCATCTTTGCC[-/ACAGTGAGAT]GCATGTGTTTCCACC	78514
rs254657505	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77505362	GATAAGACATGCTCC[A/C]CTAGAGAACTAAGAG	78514
rs254662644	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77311985	CTAAAAATTACCCTA[C/T]ACCAATAAAAATAAG	78514
rs254673338	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77288525	CAACAAAGTCAGGAG[A/G]CCCCCTCACTGCTCA	78514
rs254676101	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77319241	TACCTAATAAAAAAG[A/G]AAAAAGGAAAAAAAA	78514
rs254679696	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77409410	ACAGTGACCAACGAC[A/G]GTTCACAACAAAGAT	78514
rs254683346	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77323987	AAAGACTCCCTCCAC[-/T]CCCCCCCATCCCCTC	78514
rs254696433	in-del	-/CCTACGCCTG			intron-variant	Arhgap10	Mm_Celera	8:77490237	CTTAGCCAGCTCCAC[-/CCTACGCCTG]CCTACACCTGCCTAC	78514
rs254696491	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77508533	AGAACTCACTGTGTA[-/G]ACCAGGCTGGTATAG	78514
rs254696986	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77512146	TACATATCTTGAGTG[C/T]GTCACAAACAAAGGT	78514
rs254701046	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77419993	ACCAGCCTGGTCTTA[A/G]TAAGATTTTGAGACC	78514
rs254709870	snp	C/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77458410	TTCAGTTTCCAAGGG[C/G/T]CAAGATGAGTCATCA	78514
rs254730236	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77462965	GTGGCCCAGTGGACG[G/T]TAGAAGCACAGCGAC	78514
rs254734911	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77329826	GTCTGACACTCTCTT[C/T]TGTCCTACATGGGCA	78514
rs254742489	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77363581	TAACTTCTATGTAGG[C/T]CTTAGAAACTAAACT	78514
rs254751172	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77432118	CAGGAAGTGTGTGGT[-/G]GGGGGGGGGGGTGGA	78514
rs254757656	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77312592	TTTGAAGATGGGATG[C/T]CCAGATAAGGCTATC	78514
rs254761970	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77267899	TGGCTACAGAGGTCA[C/T]CTCCGTTGCTGCTTG	78514
rs254769986	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77511318	GCCCTGAGTTCAAAT[A/C]CCAGCAACCGCATGG	78514
rs254791526	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77323978	ACTGTAGGAAAAAGA[C/G]TCCCTCCACCCCCCC	78514
rs254815593	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77421575	TTTATAAAAACAAGT[C/G]TAGTATTTGTCTGGT	78514
rs254832480	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77447608	AGCTCACCTACAGCT[-/C]CCGCCCGTCTGCTCT	78514
rs254849994	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77397850	AACCGAAACGTTCGG[C/T]AGCACCACTGCTGGG	78514
rs254860097	in-del	-/GTGTGTGTGT			intron-variant	Arhgap10	Mm_Celera	8:77489256	CCCTCTCTCTCTCTG[-/GTGTGTGTGT]GTGTGTGTGTGTGTG	78514
rs254875533	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77403996	TGCCACTCCATTCAC[A/G]TGTACGTATGTGCAT	78514
rs254878859	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77430971	CTGTGCCTGCTTTTT[C/T]AAGAAGCTCTTCAAA	78514
rs254885418	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77424516	CTCTTTATAAACTAT[A/G]AAATATCATCCAAAC	78514
rs254903792	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77413143	CTGAATCATCCCTCC[A/T]GCACCTTCCCTAATA	78514
rs254904245	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77412995	TCTATAACCATCCAC[C/G]GTATTCCTAGTATCT	78514
rs254905349	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77473468	TGGAAAGCAGACTGT[A/G]CAGCGGAGTCCACTC	78514
rs254909012	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77356201	CAGGGGCTGCAGAGA[C/T]GCCTTAGAAGTCAAG	78514
rs254911098	in-del	-/AAAAC			intron-variant	Arhgap10	Mm_Celera	8:77329929	TTAAAAAAAAAAAAA[-/AAAAC]CATGTTTGTGAGCTG	78514
rs254912918	in-del	-/AA			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485544	CAGACTTTGTCACCC[-/AA]AAAAAACCTTTCCAG	78514
rs254915628	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77295096	CATTACTTCTTCATT[C/G]TCCCTGCCCTGAAAG	78514
rs254916272	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77467639	ACCTTCCAAAAGCTG[C/T]TTTTATCAATTACTA	78514
rs254935910	in-del	-/GC			intron-variant	Arhgap10	Mm_Celera	8:77346216	GGGATACACGGTCCA[-/GC]GCCAAGAACAACAGC	78514
rs254945733	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77380677	TCCACAGAGCACAAA[A/C]AAACAAAAAAACAAA	78514
rs254954386	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77287981	AAAAGTGGAGGTGCC[C/T]GCACAGAGTTAAACC	78514
rs254960056	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77438574	AAAAAATTCTGCCAT[C/T]GAGAAATCATTCCAT	78514
rs254961246	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77505602	GTTGCGGGGGCCAGC[G/T]GTGTCTACACTGTGA	78514
rs254968023	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77418745	CGGTTCTCAGCCTAT[A/G]GGCCACCACTCCAGG	78514
rs254980628	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77408793	TTTATACAACTAGTC[G/T]TCAGGGAATTTACTC	78514
rs254981818	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77479758	TACACAGAGAGACAG[A/T]AAGATGTGAATTGTG	78514
rs254989082	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77379281	GTGTCACAAATGTCT[C/G]TGTGGCTTTAGTCCT	78514
rs254993213	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77281573	CTTCTGACTACTCAC[C/T]AGGCACATCATGGAC	78514
rs254998128	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77457943	CCACAAATGTAGTGG[C/G]CACActatctatcta	78514
rs255002552	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77445917	TTAGGCAGTGGCCCA[C/G]CTATTGTGTTGTTCA	78514
rs255016667	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77334849	GGAAGGGCAGGGAGG[A/G]TAGGCAGGGAGAGGG	78514
rs255027873	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77505014	TATGAGCCCATAGGG[A/G]CCAGCAGCCTAAAGG	78514
rs255029682	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77485920	CCTTTCACAGGGGCC[A/G]CTTAAGACCACCAGA	78514
rs255038174	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77491668	CAAGGGGTATGGCCA[G/T]AGCTCCCGTGGCCAC	78514
rs255041435	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77318498	AACAGCCTGCCTTTC[C/T]AATTCTTTCCACCAA	78514
rs255047719	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77409141	ACCTCACTGGAAGGG[C/T]TTGCCTATGATCGCC	78514
rs255059398	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77344819	TATTGATTTAGAAAG[-/AA]AAAAAAAGTCTTAGT	78514
rs255065019	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77413341	GGCTGCGGAGCTCCA[C/T]GCTACTGCAGAAGCA	78514
rs255078767	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77329386	TTTTCTTGTTTATCC[C/T]TATCTTTTCTGTACA	78514
rs255083232	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77439582	AATGAAAAGAAAAAA[A/G]TCAAGTCTATGAATT	78514
rs255091100	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77266870	AGGGATTCCCACTTG[A/C]CTTCTTCCAAAATGG	78514
rs255094383	snp	A/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493648	CAATGGAACCACTGG[A/T]GATGGACTAAAGCCT	78514
rs255105803	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77384861	CAGAGTCAGTCAAGT[A/G]AGAACACACAAACTG	78514
rs255114596	in-del	-/AAG			intron-variant	Arhgap10	Mm_Celera	8:77464443	AGAACCTTCTTGTGC[-/AAG]AAGGACGATTTCATA	78514
rs255128250	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77273215	CAAACAAGAGGCACT[A/G]CTGTGTTAATGACAA	78514
rs255132944	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77457849	ACTGGTTCTTTTGTT[-/A]TAAAAAGTTCTAGTA	78514
rs255136003	in-del	-/AGAT			intron-variant	Arhgap10	Mm_Celera	8:77289365	AAAAGTAGCCCTGAC[-/AGAT]AGATGCCCAAGACAG	78514
rs255147975	snp	A/G			synonymous-codon, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77517748	CCACGGGCTGTCGAG[A/G]TAGCAGTCGCTAAAC	78514
rs255148501	in-del	-/TCC			intron-variant	Arhgap10	GRCm38.p3	8:77471646	CTCTCCAACTCCCCT[-/TCC]CCCCCCCCTTTTTTT	78514
rs255152937	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77288391	GGATTGCTGCAGCTT[A/G]CGATTGCTTTGAAAG	78514
rs255158197	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77426201	ATCGCTGCCCCGTTT[C/T]ACAGAACCCCACTCC	78514
rs255160146	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77253234	TTCCTAGGGCCCCCG[-/T]TTCTCTACAGTCTCA	78514
rs255161399	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77403107	AATATAAACAGATAA[A/G]CTGCGGGGATAAAAG	78514
rs255161491	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77397061	GCTTTGCTCTGCCCC[A/G]CTATTTTTCACTGAT	78514
rs255190953	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77263039	AACAGGACTCCAGGC[A/G]CGGCCCATGGTACAA	78514
rs255203698	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77378105	ACTCAGACCCCAGGC[A/C]CAGCACATTCATTCA	78514
rs255208636	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77311749	ACAGACGCTGCAACC[A/G]CAGGCAACCGGCACG	78514
rs255230789	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77287421	ACACCATAGTGGCCT[-/C]TCAAATGTTACCCAT	78514
rs255237295	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77384739	TAACAAACAGGATAA[A/G]GGAACACTCACCTCC	78514
rs255239882	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77441867	GGATTTACTCCCAAC[G/T]TAGCACCCACTTTAG	78514
rs255242402	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77280591	CTCCTAGTAGTGTGG[C/T]CTGTCAATATTTTTG	78514
rs255251714	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77340729	CCACTAGTGTCACGC[A/C]CACCCTGTCCACACC	78514
rs255257292	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77413404	GGGAGGTGGCTCAGC[A/G]CTTCAGAGCACTTTC	78514
rs255264544	in-del	-/GTGA			intron-variant	Arhgap10	Mm_Celera	8:77270601	AGCATGGAGGGAAAG[-/GTGA]GTATGAAATCCCACC	78514
rs255272217	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77378393	ACTGGCATCTAGGAA[A/G]CAAGGCTTAGCAGGA	78514
rs255277056	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77281182	CTGACCTCCACCAAA[C/T]ACTCGCCAACACCTG	78514
rs255278007	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77372582	CATCTTTCTTCAGCC[A/G]CCCAAGCATCTGCGT	78514
rs255294625	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77287112	AGCTACTGTATAAGT[-/A]AAAAATCTACCCTCA	78514
rs255304815	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485124	AGGAACTAACAGCCA[C/T]CTCCCCTGATCAAAA	78514
rs255314413	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77412139	AAAGCAACGGTACAA[A/T]GATTATTCTACATCC	78514
rs255328617	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484918	AGTTTAAAAACTGGC[A/G]TGCTTCTGCTCCACA	78514
rs255330282	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77261720	GACCTGGACCACCTA[A/G]CTACAAAATACACTA	78514
rs255344483	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77372948	TCCCACCTGCAGGGA[C/G]GAGGAGGTTGCTGTT	78514
rs255353472	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77272267	ATTCTTCAGGAACTG[A/G]GATAAGCATTAGTTC	78514
rs255358922	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77406620	CAGGGGCGGCAGGCT[A/G]AGGGTCTGACAGGCT	78514
rs255369911	snp	A/G			intron-variant, synonymous-codon	Arhgap10	GRCm38.p3	8:77491990	GTCGTCCACTGCCAC[A/G]GGGTGGCTGGCAAGC	78514
rs255393806	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77360024	GGACACTCATGGTGG[G/T]CCTCTTCCCGAAGGA	78514
rs255394805	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77266403	GGTATAGAGAGGAGC[A/G]CTGTAAGGGGAAGCA	78514
rs255394931	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77272629	TCTCTCCCCTCTTTT[C/T]TCCCCTCTTTTTTTG	78514
rs255400695	in-del	-/AG			intron-variant	Arhgap10	Mm_Celera	8:77402695	TATTATGACAAAAAA[-/AG]AAAAAAGAAAAAGAG	78514
rs255407087	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77407707	TACAGGAGCCTCAAC[A/T]GAGGGAGGAGAGAGG	78514
rs255414923	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77455415	TTCCTAGAGGTCTAG[C/G]TTGAGTCAAGTTGAA	78514
rs255416718	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77423439	AGGAGAGGACCACAG[A/G]GGAGAGAAGATACTG	78514
rs255417845	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77401481	TGGCTATCAATGTAT[C/G]ACTACCTACGAAATC	78514
rs255430634	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77361391	GGGCCATTTTCTTTC[C/T]TTTGGAGAGTTGAAG	78514
rs255433842	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77398038	AACTCTTCCCACTGC[C/T]GTTCTAAGAAACAGA	78514
rs255437522	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77384283	GGCCACTCTTGCTTT[G/T]TATTACTCATTGTGG	78514
rs255440265	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77255142	ACTGAACTCATGGGC[A/G]TCACAATGAGAGACT	78514
rs255445929	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77466626	GTGCTGCTTACCTGC[C/G]TGCTCCTCCCAGCTT	78514
rs255456208	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77307656	CCTATGAAATCACCG[C/T]AGACTAAGGCTGGTC	78514
rs255465995	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77429468	CAAGTGTGCCAACAC[G/T]GACTAGAGCCACTGT	78514
rs255466508	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77455011	GTGGAAGCTGATGTA[A/G]CGTCTCTCAGAATAG	78514
rs255469720	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77414587	AGCCAATAGAGAAAG[-/A]AAAAAAGAACTTTTT	78514
rs255492665	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77317118	TGTTCACTTTTTCTC[A/G]GAACCGGAAGCATCC	78514
rs255494622	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77353851	TTAATGGATTTCAAC[A/T]TGCTACAATGATTAT	78514
rs255498769	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77472415	AAGAGGTTAATAGCA[C/T]TGGCTACTCTTCCAG	78514
rs255499069	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77284765	TCTAGGTGGACAGGG[-/C]CAATCAACTAAGGGC	78514
rs255518141	in-del	-/TTTTTT			intron-variant	Arhgap10	GRCm38.p3	8:77327866	TTATATCTTCCAGGG[-/TTTTTT]TTTTTTTTTTTTTTT	78514
rs255535865	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77261445	ATGCTCTGCTCCTCA[A/T]AACTCTCCTTTCCTG	78514
rs255537758	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77496494	CCTTCCTCTTTTCTT[G/T]TCTCCCTGGTCCCCC	78514
rs255538776	in-del	-/ACTTCCTCAGCT			intron-variant	Arhgap10	Mm_Celera	8:77469114	AGCTGCAGTTTGCAG[-/ACTTCCTCAGCT]ACTTCCTCAGCAACA	78514
rs255545778	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77332283	CTGCTTGCCTAAAAC[A/G]ATTCAGATGCTACTT	78514
rs255555639	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77410115	AACCCCAATTTACTG[C/T]AACAGCAAACTCAGG	78514
rs255556707	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77346027	CTAAAGGGCACATTC[A/C]GTCTCAGCATTAGAT	78514
rs255561233	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77383613	CCGACTATGGCTAAC[A/G]TTATATAAAACGCAA	78514
rs255563974	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77448064	ACAGCTACCAAGCCC[C/T]CGGATTTCAACCAAT	78514
rs255582238	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77266730	AAAACTTCTGCTTCG[C/T]TCAATGGCAAGAAAC	78514
rs255583338	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77339332	CATCACACCGAGAAG[C/T]CAAAATAAGACATTC	78514
rs255586486	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77479791	TGCTGGTCTGACTTG[C/G]AACTGGTGACCACCC	78514
rs255600170	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77367775	AGTCACATTCAAACA[A/T]ACTCGAGCATTTATG	78514
rs255607405	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77361023	TTAATCATCTATTAA[A/G]TGCTCGCTGTTTTCA	78514
rs255611451	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77286520	GCAGGCAAGCATGCA[A/T]GGTACTGGAGCAGTA	78514
rs255631632	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77447804	ATCATTCAGAGGTTT[A/G]GTTCATCATCATCAT	78514
rs255646628	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77479124	GCTCCTCCCTCCCTC[C/T]CTCCACTGAGTAAAA	78514
rs255650930	in-del	-/GAGG			intron-variant	Arhgap10	Mm_Celera	8:77496973	AGCACTTGGGAGGCA[-/GAGG]AAGGCAGATTTATGA	78514
rs255657719	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77333825	TCACCACTGAGCTAA[G/T]AAAGCTTCAGGAAGA	78514
rs255670005	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77260777	CAGGGCAGGAACTCA[A/T]GCTGCTCACGACTTG	78514
rs255673257	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77361435	ATGTGTTGTGTAAAT[A/G]TGCTTTATCACCTCG	78514
rs255678638	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77326730	ATATAAATAGCTTCC[C/G]CCTTCCAGGTTAGAT	78514
rs255684618	in-del	-/TTGTC			intron-variant	Arhgap10	Mm_Celera	8:77443034	GGAGACGGGGTTAAT[-/TTGTC]TAGGCTTGGTTGTCC	78514
rs255687466	in-del	-/CA			intron-variant	Arhgap10	Mm_Celera	8:77405328	TCAATGTACATCCAT[-/CA]CACTCATACCCAAAC	78514
rs255692947	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77371571	TCTCTGCTACCTCCC[G/T]TCCTCGGGGTAAACT	78514
rs255700353	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77466170	ACACAAAATAGAGTT[G/T]CTAGAAGGTTAGTCC	78514
rs255715958	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77459385	AAAATCAAAGACAGA[A/T]CAAACTGGAGGCAGT	78514
rs255719985	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77278731	TCCCAAAAAGAAGCA[C/T]AAGACAAATCGTGGG	78514
rs255721743	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77381534	CGGACTGGCTTCAGT[A/G]GATGACCTGAAAGGG	78514
rs255732175	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77298550	GAAGTCTAATATTGG[G/T]CTGGAGAGATGGCTC	78514
rs255741775	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77253050	GGGCTATTTTTGAGT[A/G]CTGCTGCTGCTGCTG	78514
rs255741847	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77490789	TGTAATGAACTCGGG[A/G]AAATTATGATGAAAC	78514
rs255748490	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77337123	TTTGGGTTTTGTCTG[A/G]CAGGTGAGGGCGCTG	78514
rs255754603	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77372089	CTGCCCTTACTTTCC[A/G]TTCATACAAAACAGA	78514
rs255783203	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77464609	TGAATTCCCTGGTAT[A/G]TTAAATGTCCAAAAG	78514
rs255795318	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77455353	TGAGCCGGAGACACG[G/T]CCACAGGCCAATACA	78514
rs255803198	in-del	-/ATCA			intron-variant	Arhgap10	Mm_Celera	8:77489130	AGCCTGTCTCAATCT[-/ATCA]ATCGATCAATCAATC	78514
rs255808469	in-del	-/CAGCCTACAAGCATGACACAGACCTTGCGGGA			intron-variant	Arhgap10	Mm_Celera	8:77460535	AGGGCAGGGTCACCT[lengthTooLong]CAGCCTACAAGCATG	78514
rs255833376	in-del	-/AATGAATGAATA			intron-variant	Arhgap10	Mm_Celera	8:77422425	AGCAAAAGCTGAATG[-/AATGAATGAATA]AATGAATGAATGAAT	78514
rs255836322	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77315771	TCTTGTCATTATTTG[C/T]TATTCTATAAAAATG	78514
rs255837230	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77471646	CTCTCCAACTCCCCT[C/T]CCCCCCCCCCTTTTT	78514
rs255851792	in-del	-/A/AA/TT			intron-variant	Arhgap10	GRCm38.p3	8:77487102	CTGACACTCAACACC[-/A/AA/TT]AAAAAAAAAAAAAAT	78514
rs255852716	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77265883	TCGCTGGCTCAATCT[C/G]CATCACCCTAACATT	78514
rs255871193	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77291699	TAGTCCTGGCCTTGT[C/T]GACAACAGCTGCCGG	78514
rs255879153	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77427958	AGCAACCAATAAAGA[A/G]TGGAGTCTGCCCTTC	78514
rs255880771	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77483528	TAATGAGGAACAGAG[C/T]GCCTGCCTGCCTGGG	78514
rs255881446	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77421291	TCAGATGAAAGGCAA[C/T]GCACATCAGACATAA	78514
rs255893786	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77453036	ACACTGAACCAAGAA[A/G]GAGCAAAGGTCCTTC	78514
rs255912298	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77312813	TTTTGCTTTGCTTTG[A/C]TTTACATTTTAAAGC	78514
rs255914060	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77331713	ACAAAGACAACCAAA[C/T]TGATCTCTGACCTCC	78514
rs255915310	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77454494	GCTTGTCGCCTAGCA[G/T]TCACAGTAAACTAAG	78514
rs255923423	snp	C/T			synonymous-codon	Arhgap10	GRCm38.p3	8:77344766	CCCTAAATTCGCCAC[C/T]GTCATTAGATTCTGC	78514
rs255924318	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77514822	ACTGCAGGAGTTCAC[G/T]TCCACAGCCCAGGCT	78514
rs255936890	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77256641	CCAAGGTTTCCCTGC[G/T]TCCTAGGAACTCTTT	78514
rs255949190	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77447496	AAAGTGGTCACATAG[-/T]TTTTTCCATAAAAGT	78514
rs255962783	in-del	-/AT			intron-variant	Arhgap10	GRCm38.p3	8:77377808	TCAGGATAAGTACAC[-/AT]ACACACAGACACAGA	78514
rs255976625	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77337825	CCTTATCGCAGCCCT[C/T]CCACCCTCTGGCTCC	78514
rs255982745	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77454127	GACACCTGGAGAAGC[A/G]CACGGGCTGGGACCC	78514
rs255996824	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77396460	ACCTGCTGAAGCAAC[A/G]CTCTATTAACGACAA	78514
rs256018491	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77443855	AACCAAAAAAAAAAA[A/G]AAAAAAAAAAAAAAG	78514
rs256019142	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77252903	GGCCTATTTCACTTA[A/G]GAGATCCTCAGGTCC	78514
rs256027342	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77416665	GACGGACAGACAGAC[A/G]GGCAGGCGGACCTCA	78514
rs256029007	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77459984	CCTCACCATACCCCA[A/T]TAGGTAAGGTCAAAG	78514
rs256033630	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77514270	CATGAAACCTCCCTT[C/T]CAGCCACCTCACTCT	78514
rs256034532	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77383703	ATAAAGAGCAGAGAC[-/AA]AAAAAAAGGGGAAGA	78514
rs256037290	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77338368	ACTTGGTATCATTTG[A/G]GTCATAATGGCAAGG	78514
rs256040222	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77314344	CTTGTTTTGCTGTAC[A/C]TTTCCAAAACATCTT	78514
rs256055403	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77326259	TGATTGATTGACTGA[C/T]TGATTAAAAGGGGGG	78514
rs256058945	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494592	ATGTTCTTGTTCCAG[C/T]TGCGAGTTTAAAACC	78514
rs256064468	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77460104	AGCCTGCTCTACAAA[A/G]TGAGTTCCAGGACAG	78514
rs256084520	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77403810	CTTTCAGGGTTTGCT[-/C]CAAGCACTCCAGCAG	78514
rs256084987	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77319967	ATGAATTCTGCCTTC[C/T]CTTATTCATTTACTC	78514
rs256090622	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77257962	TAGAAGCTGTACTGG[C/T]TGGTTTCCTGTGTCA	78514
rs256090724	in-del	-/TT			intron-variant	Arhgap10	Mm_Celera	8:77296131	AGGAGGATGTAGAAC[-/TT]TTAGCTCCTCTTCAC	78514
rs256096828	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77429442	GAGCCAGTGAGCATG[A/C]GCTCACAGCACAAGT	78514
rs256104833	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77427309	AAATATCCCAGCTTC[A/T]GCCTGCAGAGATGAC	78514
rs256117829	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77297403	ACCTCCAGTTCCACA[A/G]GATCCAATGCTCTCT	78514
rs256120456	in-del	-/A			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77504019	AAATGCTGCCCCAGG[-/A]AAAGGCTTATAAGGC	78514
rs256134845	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77414985	CATGTCACCACCTGC[A/G]GCATCTCCCATGTCT	78514
rs256141750	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77400087	TCTCCAAAGTGGGGG[A/G]ACTGAGACAGGAAAA	78514
rs256143218	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77470238	TGCGGGTGCAGACTG[A/T]CTCACAGAACGACAG	78514
rs256155424	in-del	-/CCCAGAG			intron-variant	Arhgap10	Mm_Celera	8:77260957	GATGCTGGGTTGAAA[-/CCCAGAG]CCTTGCACTTGCTCA	78514
rs256165952	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77436638	AGCTGCTAGCAAAGC[C/T]GGGCTGAATATAGAA	78514
rs256172379	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77434339	CCAGAGTGTGATTCC[C/T]CAAGACCCTCACAGT	78514
rs256189047	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77421159	CGCCAGCACTTGGGA[A/T]GCTACGGCAGGAGGA	78514
rs256190372	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77414481	GCAAAATGCTGGCGC[A/C]CTGGTTCCTTCCTCC	78514
rs256192649	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77478152	TACTGGTAATTACAA[C/T]GCACAATAAGTACCT	78514
rs256201466	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77409220	CCACGCTGCTATGGC[A/G]AGCACTGTCTCTAAC	78514
rs256207975	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77475688	ACCTCCCCTGCCTCT[A/G]CATACACACATATGC	78514
rs256212738	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77366150	AATCACCAAAGGTCA[C/T]GGGCTCTGCTCACAG	78514
rs256224792	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77298051	GTGGAATAATCTCCT[C/T]CTGGCTGTCTTTAGA	78514
rs256229612	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77363175	GTGTGTGCTCAGACA[C/T]CTACATGCAGATGAA	78514
rs256235865	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77344034	CTGGCCCATGAGAGT[A/G]AATCCTCGTGACATA	78514
rs256237458	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77435123	GAGTGACGTACAGGA[C/G]CAGACCATGACAGTC	78514
rs256243533	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77274907	TGAACTAACCAGTAC[C/G]TCCCAGAGCTCGTGT	78514
rs256252769	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77328686	TCCATTATACTAACA[-/C]CATAAATGGGTAGCT	78514
rs256253457	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77282560	CAGGTTTGCCTACAG[C/T]CTGATCTTAGAGAGG	78514
rs256260060	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77291061	AAAATTCTAGAGCAG[C/T]CACTACAGCATTGTA	78514
rs256270265	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77321381	TCTTATGAACGACCC[A/G]GTCATGGACTGAGTC	78514
rs256292311	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77359956	TAAACTCACGTGTGC[A/G]TCCTAACACATCAAG	78514
rs256292896	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77434485	TATAACACCTGTGTC[C/G]ATCTCAAAGCTTCTA	78514
rs256298175	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77355405	ACATAGAGGAGGGGA[-/G]GGGGAGGAACCATCA	78514
rs256299216	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77356998	TTAAAAAACAGTCAC[C/T]AAGAAGCACCGCTTG	78514
rs256301242	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77441762	ACACACACACACACA[C/T]ACACACACATACAAA	78514
rs256302885	in-del	-/TTTT			intron-variant	Arhgap10	Mm_Celera	8:77354212	CATGAAGAAAATCTA[-/TTTT]TTTTTAAAAAAAGCT	78514
rs256306323	in-del	-/TG			intron-variant	Arhgap10	Mm_Celera	8:77411468	ATGTATACACGTGCA[-/TG]CACACACGTGCACAC	78514
rs256308553	in-del	-/AAG			intron-variant	Arhgap10	GRCm38.p3	8:77464982	GGTACGTAAGATTAC[-/AAG]AATACAGGAAAATAA	78514
rs256312767	snp	A/G/T			intron-variant	Arhgap10	Mm_Celera	8:77431921	GAGAGGGGAGAGGAG[A/G/T]GGGAGGGGAGGGGAG	78514
rs256318752	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77385847	AGTAATGTCTAGTCC[A/G]CTGCTTCCTGTTTCT	78514
rs256322591	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77388953	ATTGCGGGAGGGGTG[C/T]CTTACCATGTAGCTC	78514
rs256325134	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77435414	TCCGAGATTCTGTAC[A/G]TGCAAAGCTACCTAA	78514
rs256327912	in-del	-/TT			intron-variant	Arhgap10	Mm_Celera	8:77312868	TAGAGCAAAGAAACA[-/TT]GACTTGGGAAGTCAA	78514
rs256350436	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77474347	ATATACTCACACACG[C/T]GCATGCCCAAACACA	78514
rs256352534	in-del	-/AG			intron-variant	Arhgap10	GRCm38.p3	8:77441018	GACACAGGGGAAAAA[-/AG]AAAAAAAGGCTACAA	78514
rs256355668	snp	C/G			intron-variant, missense	Arhgap10	Mm_Celera	8:77476589	TGGCTTCAGTACTAG[C/G]CAGCAACTGTGGGCT	78514
rs256356919	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77269350	GAGCCACCAGCCTGC[A/T]CTAAAGCAAAAAGGC	78514
rs256357260	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77274463	TCTGCAAGGCTAGGT[G/T]CCTCCTCTCCCACGG	78514
rs256361446	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77441096	TCCCAAGGGGCTGAC[A/G]GTTAGATGAGGATCT	78514
rs256364040	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77344998	TCCCGCTCCCCACTG[C/T]CCCCTTCCCTGCTCT	78514
rs256364723	snp	A/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494771	ATGTGTCTAGAAAGC[A/T]GGGCTGAATAAACCA	78514
rs256372436	in-del	-/TTG			intron-variant	Arhgap10	Mm_Celera	8:77479862	GGCTCAGACCCGTTT[-/TTG]TTGTTGTTGTTGTTG	78514
rs256379695	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77380532	CTTTCTGATCTAGAA[G/T]GTTTTTATCTAAAAT	78514
rs256391170	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77453796	CAAGGAGCTTCCCTT[-/C]CCAGACACCCCTTCC	78514
rs256392776	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77325656	CACTCTTTTTTAATG[A/G]CCCCAATATATTTTT	78514
rs256393320	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77382286	TGTTTGCACACAGAA[A/G]GGACATGTATGCACA	78514
rs256394155	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77319581	TATGACAATTCCTTT[A/G]ATAATCTTCATTAAT	78514
rs256405173	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77270015	AGCAAACTAAAGTAC[A/G]AATAAGGAAAGAGTG	78514
rs256411379	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77335875	ATTTTCCTCTGCACA[A/C]GTCCTACTCTGATGG	78514
rs256415923	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77480331	TGAGTCCATGAAGCT[C/T]TCTGTCCATCTTTGA	78514
rs256429968	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77296684	GAAGTCAGATTTACC[C/T]TACTCTATGAGGCAA	78514
rs256434690	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77482669	GACATCAAAACTGTC[A/G]CCAAGCAGCCAGCTT	78514
rs256445490	in-del	-/AAT			intron-variant	Arhgap10	Mm_Celera	8:77353886	AGTATTCTAAGTCAA[-/AAT]AAGTTTTTGAAGTAG	78514
rs256445595	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77399303	ACTGTATTAAAGGGT[C/T]GCAGTATTAGGAAGG	78514
rs256446617	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77338183	ACTGATGGCTGCTGG[A/G]AAACTGTCATCTGCA	78514
rs256453327	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77281401	GGAAACGCGATGGGC[C/T]CTCTGTTACAAGAAA	78514
rs256459540	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77495853	GTTTACAGGAGGTTT[-/A]ACCCCGCACAGCTGC	78514
rs256460834	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77404900	GCCTCCTGAGTGCTG[G/T]GATTAAAGGCGTGTG	78514
rs256475199	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77330249	ACTAAGAGGGAAGGC[A/G]GTGAACATAGAAAGA	78514
rs256487018	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77273517	CTAGAAGCTGGGGGA[-/G]GGGCCAAAGATTAAG	78514
rs256489505	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77273795	ATTAACAAAACAGGA[A/G]GAGCCCACTTACCTT	78514
rs256490764	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77284924	TGCACAATACAGACA[A/G]CACAGCAGGTAAAAC	78514
rs256496952	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77319252	AAAGAAAAAAGGAAA[A/G]AAAAAAAAAAAAAGA	78514
rs256502840	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77386551	GAAGAGAGCTACAGT[A/G]TACTTATGTATAATA	78514
rs256508735	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77289495	GCGTTTGACCCAGGT[A/G]CTCAAGGAGCCGGGT	78514
rs256510790	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77480622	CTGAGTGTTTTGCTC[A/G]TATGTACATCTGTGG	78514
rs256525647	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77317916	CCTGCCTGTATGAAA[A/T]TATCTCATCTATACT	78514
rs256529264	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77276104	CACTATACATAATCC[C/T]CAGCACAGATAATTA	78514
rs256531988	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77500576	TGATACACACATTGG[C/T]CCTACCACTTACCTT	78514
rs256535404	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77469653	AGCTCACTACCATCT[A/G]TAACTCCAGTCCCAG	78514
rs256535469	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77399569	ACTGTGTATTTCATT[A/G]ATTCCACCACTGCTT	78514
rs256544632	in-del	-/CC			intron-variant	Arhgap10	Mm_Celera	8:77378865	AGGACGAGTGAGCTA[-/CC]CCCCCCCCATGGGCT	78514
rs256545405	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77290236	AAACAAACAAAAAAA[A/C]AAAAACCAACAACAA	78514
rs256558495	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77502841	GTACCAAGCTCTGGT[A/G]ATGACACGTCTTCTA	78514
rs256564786	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77355752	TCAAACACAACGTGC[A/G]CATGTGAATACGAAG	78514
rs256569328	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77486465	GATCTGTTTGCATTT[A/G]CATCCTGAATGCTGG	78514
rs256571137	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77320097	GTTTTACGGTAGCAG[A/G]AACTATCTAAAAGTA	78514
rs256578329	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77472573	AATAAATCTTTTTTT[-/A]AAAAGATATATGTGT	78514
rs256582665	in-del	-/CCCC			intron-variant	Arhgap10	Mm_Celera	8:77387882	CATCTTCAGATCATG[-/CCCC]CCCCCCCCCCCAAGT	78514
rs256600596	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77380654	AATTAAAAAGCAGTA[A/G]TTAGTGATCCACAGA	78514
rs256611413	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77369585	CATGAATGCTCACTA[A/G]TGCACAGTAGTAATT	78514
rs256612798	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77311354	CAATTACCTGTCTCG[A/G]TTCTTATTTACATTC	78514
rs256617818	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77506969	ACAGGTCCAAAGCAA[C/G]AAGCCTAGGGACCAT	78514
rs256620885	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77255291	GGAACTATTGAGAAG[A/C]CCTGGGTGTTCCAGC	78514
rs256623589	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77420618	AAGGATCCACAGCAA[A/C]GAGTGTCCTGCTACT	78514
rs256645712	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77314250	ATTATATCCTTTTTG[A/C]GTCTCAAGGAGGAGA	78514
rs256661706	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77508766	TGTAGCCAAGGTAGT[A/T]AGGAGACTAAAGCAA	78514
rs256664876	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77374659	GGTGCTCTTGGTAAC[G/T]GAGGGTGAATGAAGC	78514
rs256666898	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77381031	CAGTCAGTGTGCTTT[C/T]ACAGTGTGGCCCCTG	78514
rs256667501	in-del	-/T			intron-variant	Arhgap10	GRCm38.p3	8:77441738	ATCTGTTCCCCACCC[-/T]CCCCCCCCACACACA	78514
rs256677250	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77257920	TGTTCCGAGCCCTCC[C/T]GAGAGAGGCGCAACA	78514
rs256679749	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77263055	CGGCCCATGGTACAA[C/T]TCACCTTCATCGGCT	78514
rs256683043	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77269157	GCTCACATCCCTGAC[C/T]AGTCACGCGCCAGCC	78514
rs256706165	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77421406	AGTCACGGCTTCCCA[-/G]GTCAGGGCTTCTGCT	78514
rs256716920	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77263522	CATGTACCTAATGGA[A/G]CCATCTCTGCTCTCA	78514
rs256721209	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77273886	GCTGTGGTGTGGCTC[A/C]GCCCTAGCATAAACC	78514
rs256740177	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77504929	CCCCAGTGGCACAGT[C/T]CCTCCAACAAGGCCA	78514
rs256748859	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77499767	TTACAAAGCAGGGAC[-/A]AAAACCCTTATGTTT	78514
rs256749901	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77513461	AACTGAACTTCTTCT[C/T]GTTCTTCCAAATCGC	78514
rs256763634	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77487757	GAGAAACAGGCTGTC[A/G]GTGTGTGAAGAAAGT	78514
rs256765845	in-del	-/GCTGGTCTCGAGTGA			intron-variant	Arhgap10	Mm_Celera	8:77469504	GGAAGGTTAAGAACC[-/GCTGGTCTCGAGTGA]GCAGACATTTGTTCT	78514
rs256783839	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77513044	TGCCACTAAGCCTGG[C/T]TCATGGGAGCTGGGG	78514
rs256793228	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77507096	TTATACGATCATGAG[A/G]AGCTGAGTTTGGATC	78514
rs256794431	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77255192	CGCAGGGCTCACAGA[A/T]GAGGCATCCACACCC	78514
rs256807861	in-del	-/CA			intron-variant	Arhgap10	Mm_Celera	8:77289184	ATTGGTTGGAAAACT[-/CA]GTTTTATAATACACA	78514
rs256818315	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77373881	GTGAGGTCACAGAGA[C/T]GCAGTCTGGTACCAG	78514
rs256847619	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77467976	ACAGACACATGGTAG[C/T]CATTTTCATATTAAT	78514
rs256852764	in-del	-/CC			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77503971	CGGAACCCTCATGAG[-/CC]CCCCCCCCCTCCAGC	78514
rs256858908	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77430275	CTCACACAGACCCAC[A/G]TCTGCACTGCTACCT	78514
rs256865546	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77356519	TGAGCAGCACTCACA[C/T]GACACCTATCTCTCC	78514
rs256871389	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77445742	AGAGCAGCCATGCCT[G/T]AGAATGGTGCAGGAC	78514
rs256881331	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77408405	GGCCCTGTAACACAG[C/T]AGTTTTAAAAGACTT	78514
rs256881424	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77472940	ATGCCTACACTCAGG[C/T]GCATGCACATGTGCA	78514
rs256893653	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77323365	TCATTTTGTACATCT[A/G]CCATAGACACAGAAA	78514
rs256901498	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77362137	CGGAAGGAAAAGGAG[A/C]TGAGGAGGTCCTAGG	78514
rs256903256	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77467611	GCACGACCAACCCAT[C/G]TTCAAGGGATTCACC	78514
rs256903673	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77374519	AGAAATAGCATCCCC[-/T]TCCTTTTATAGGGAA	78514
rs256913241	in-del	-/GG			intron-variant	Arhgap10	Mm_Celera	8:77326268	ACTGACTGATTAAAA[-/GG]GGGGGGGCTGAAGAG	78514
rs256925426	in-del	-/CACACACACA			intron-variant	Arhgap10	GRCm38.p3	8:77467663	ATTACTACAGAAATT[-/CACACACACA]CACACACACACACAC	78514
rs256934732	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77371057	TAGCTAGCTATATTA[A/T]TATACATGAAAGACA	78514
rs256935456	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77349554	TGAGCTCACCAACAC[A/G]GAGCAAAGCCAGGAG	78514
rs256943520	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77450683	ATAAATGTACATCCC[C/T]GCTACTCACCATGAT	78514
rs256968539	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77450553	ACATAACCACCATGG[A/G]CCCAGAAATCAGAGC	78514
rs256973237	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77268683	ATGGTTTGTTGATAG[C/T]CACACATATAGGCCC	78514
rs256980867	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77433863	ACCCACTATAAAATG[A/G]TTTCTTCTAAAGTGG	78514
rs256986743	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77438226	TTCCACGTGTAGTCT[C/G]TCTCTGCCCTCCTCT	78514
rs256994940	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77384179	CTGAAGGACTTCTCA[G/T]TCCTCACTGCCCGAA	78514
rs257005115	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77412965	TAAGTAAAATGCTGC[C/T]GGGTAGCACTGGTTT	78514
rs257008325	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77485883	CAACCTACGGTCATC[C/T]GCCCTCTGGGGGTTG	78514
rs257012062	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77450425	TTAGGGTAACATACA[G/T]GCAAGTCAAAGGCTC	78514
rs257014779	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77340332	ACAGGCACAACAATG[C/T]CCAGCTTCATGGTTT	78514
rs257016128	in-del	-/ACAC			intron-variant	Arhgap10	Mm_Celera	8:77457891	GCGCACATGCATGAT[-/ACAC]ACACACAAAGATAAA	78514
rs257029362	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77455923	ATCTCCCCAAATTGT[C/T]TTATCCATAGTGTTT	78514
rs257031137	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77367719	GCCCCCCCTCCCCCC[C/T]GCAGAATTTAAGTAG	78514
rs257041393	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77347655	AATTTTATTATCAAA[A/G]GTTTAGAACTCTGGA	78514
rs257046028	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77399456	AAGGACTTCATGATA[C/T]AACAGAAACTCCCAT	78514
rs257054152	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77378947	ACAGGGTATGGATGA[A/G]CAAGAACTAGGCAGA	78514
rs257058070	snp	A/C			downstream-variant-500B	Arhgap10	Mm_Celera	8:77250172	AGACCAGTTCCCATC[A/C]CAAGGTCTCTTGTGG	78514
rs257063953	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77468925	AAATTACAGTTATAT[A/G]GTAATGAAAATAATG	78514
rs257069263	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77334499	GAACAAGCTAGACAC[C/T]GGTAAAGACAAAGTG	78514
rs257070892	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77275683	CCAACCCCGCCCCCA[-/G]TCCAGCTAGAAAGTC	78514
rs257082880	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77329682	CTTACTCTGCTACCT[C/T]AAGACAAGCTTTTGG	78514
rs257091894	snp	G/T			utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250775	GCCCACATCTGCACA[G/T]TCCTAGGTGGCTGTT	78514
rs257126770	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77387472	ACTTCTAAGAACTGA[A/G]CACTGCTGAATGAGA	78514
rs257134656	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77407280	GACAACAACCATCTA[C/T]AACTCCAGTTTCTGA	78514
rs257156578	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77360767	TCTCATTAAATCAAT[C/T]ATTTAAAATCTCACT	78514
rs257159060	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77340962	TTCCCATGGAGCCCT[C/T]GGCATGCTCTCCATT	78514
rs257164758	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77462154	CTTCTAAGCATTCAA[A/C]CTGGTCTATATAGGA	78514
rs257172331	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77343024	TTTCCCACTGCCCCA[C/T]GGCCCAACGGGTGAG	78514
rs257177434	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77316620	ACAATGGGCCATGGC[C/G]ATTAAAACTCTGACA	78514
rs257199503	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77474091	ACGGCCCAGCCAGTG[A/G]CTCCAACTGGCTCAG	78514
rs257202762	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77498283	TCCCCAAGAAAAGCA[A/T]TACTTCTCTTCTCCC	78514
rs257204675	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77289050	CAAACAAACAAACAA[A/G]CAAACACACACACCT	78514
rs257207851	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77260722	AACACCACTGATAGA[A/C]AGCAGCTTGGGGCGG	78514
rs257211080	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77458692	ACATCTTCTCTTGAC[A/T]GCCCAAGGAACAAAG	78514
rs257215212	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77290406	ACCGTCTAGCCTGCA[C/T]AGTGGAGCATTTCTC	78514
rs257229907	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77501505	GGATGAAGAAGACGA[A/G]TCCAGATGACCAGCA	78514
rs257240820	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77355910	TGGACAGTTTCGTTA[A/G]TGCACTAGGTATAAC	78514
rs257247933	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77336771	TCCCGGGTGAGGAGC[A/G]TCCAGCACACTTGAG	78514
rs257257658	snp	C/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77282763	GCAGCCAGTAACTTA[C/G/T]GCTAACTGTAATACT	78514
rs257260848	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77446406	AAGAAGTAATCACTA[C/G]CAAGGGTATACACAG	78514
rs257262091	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77417770	GCGTGGCTGAAGTGG[A/G]GAAGGTGGCTGAAAG	78514
rs257267294	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77423960	CTGGGCAGGTGTACA[G/T]TGCATGGCCCTATGG	78514
rs257267504	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77464297	TGGGGTCTGTGGAGT[G/T]TGGATTCTGCCTAAT	78514
rs257269437	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77430434	CAGAAAAAAGAAACG[G/T]CGTGAAAATGAGGTA	78514
rs257286038	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77446193	GCTGCCCCCCTCTCG[C/T]CAGCCATACTTCAGA	78514
rs257297991	in-del	-/AT			intron-variant	Arhgap10	Mm_Celera	8:77413340	TGGCTGCGGAGCTCC[-/AT]GCTACTGCAGAAGCA	78514
rs257303205	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77334268	GAGTCAGAGAAAGAT[C/T]TGACAGAAAAGGATA	78514
rs257308794	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77324514	TCCCACCCAGAAGAT[C/T]TGAGTTGACAGATAA	78514
rs257310960	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77354435	GTTTTCAGGGGTTGT[A/G]TTTCCAAGCACAGGC	78514
rs257313606	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77437594	CTGGTCACCTATGCT[A/G]TCAATAGGGCCCTGT	78514
rs257313797	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77285713	TAAGATCTCAACAGG[A/G]AAGTAAGGTTCCATG	78514
rs257321037	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77269321	AGGGTAGCTAAGGAA[A/G]CCTCCACAGCCCTGA	78514
rs257321103	snp	C/T			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519455	TGAATAAGAATGATT[C/T]CCACACAGGATTGGG	78514
rs257322225	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77423790	AGTAGGCAGGGGTCA[A/G]GGTATGCCTCTGTGG	78514
rs257328293	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77333368	TACTGCTTCCCCTTA[A/T]CCCCAGAAGGCTGGG	78514
rs257329537	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77413843	CCAGAGAGGCCGTGC[A/G]CCTCCTGTTTCCTGA	78514
rs257330314	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77479044	GGCTCTGCTCAGGCC[C/T]GCCCTTCCCTCACTC	78514
rs257340792	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77429801	TTACTGTTCTCCCAC[A/G]GAGCCGAAGGCCAGC	78514
rs257348433	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77362956	GCAGAGCCCTCTTAA[A/G]TGAATTATTTAATAG	78514
rs257351616	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77278007	CCAGAGGAGCACACA[A/G]CCATCAGAGCCTGTC	78514
rs257370979	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77334772	AGACTAGGCCTAGGT[C/T]TGCAGAGACAGGCAG	78514
rs257380874	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77271698	AATACCTGGTATTTC[-/T]TTAAAAAAACTTTTT	78514
rs257385566	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77323573	TTCAACCCACCAGTG[-/AA]AAATACACAGGCTGA	78514
rs257385569	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77319131	CCTAGTACAGGGGAA[C/T]GCCAGGGCCAAAAAG	78514
rs257394965	in-del	-/TA			intron-variant	Arhgap10	Mm_Celera	8:77481397	AGCACCTCATACAAC[-/TA]TATGTGTGTGGGGAA	78514
rs257410048	snp	C/T			upstream-variant-2KB, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77518438	GGAATGCTTAACGTC[C/T]CCAACTCAGCGTGGA	78514
rs257414053	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77309942	TTGAAGCAAGAAGAC[-/AA]AAAAAACAAGCAAAC	78514
rs257439067	in-del	-/ATTA			intron-variant	Arhgap10	Mm_Celera	8:77468797	ATATTAATTTCCAGC[-/ATTA]ATTAATATATACAGA	78514
rs257439374	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77329271	AGCAGTTTATCCACC[G/T]GTAGAGGAATGTATC	78514
rs257442588	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77263690	AGACAGCAGAGACTG[A/C]AACTCTCTGGAGCAA	78514
rs257461888	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77411703	GATGCTACAACGGAA[A/C]GAGAGAAGCAGCTCC	78514
rs257474680	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77327881	GTTTTTTTTTTTTTT[A/T]AATTCCTACTTGGAT	78514
rs257486983	in-del	-/TCTC			intron-variant	Arhgap10	Mm_Celera	8:77272641	TTTTCCCCTCTTTTT[-/TCTC]TTGCTATTTCTCTTC	78514
rs257491667	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77367034	CCAAAGAGGCAACCA[C/T]ATTCTCTGTGACTGG	78514
rs257497678	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77444038	CTGCCCAGACCTCCT[G/T]CGTCTAAGGTGCCTC	78514
rs257502436	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77303485	GTTTCCGGGATTGTG[G/T]GTTACTTCCATTCAG	78514
rs257511975	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77269302	CTTCCTAAGGGTAGC[-/A]AGGAGGGTAGCTAAG	78514
rs257524660	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77308669	AACTGGTTGAGTGTA[A/T]ATTATTTTTACCTTC	78514
rs257532855	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77322001	TTCTTTTCCCAAGCA[A/T]TAACAACAATGTGGT	78514
rs257533135	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77328312	TGTCCTTCCAGTTGT[C/T]TCCCTGACAACTGAA	78514
rs257534780	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77353433	GTATGAAGAACTTCA[A/C]AAAGCGTAATCTTTT	78514
rs257554049	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77440587	TCAGGGGATCCGACA[C/T]GCTCACACAGACAGA	78514
rs257556566	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77462250	GAGGGAGGGAGAGAG[A/G]GAGGGAGGGAGGGAG	78514
rs257569548	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77309554	AGATAGGTTACACAA[C/T]GCCTGACCTCTAACA	78514
rs257574328	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77396173	GAAAGAAGTCCACCA[C/T]GGAGGGCTACACGGT	78514
rs257576680	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77306715	CCTGGGCAGTTGTCA[C/T]ACAGACCCTAAGAGA	78514
rs257587392	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77481175	AAATGACCGTCTACT[A/G]TTCACACTGACTGTC	78514
rs257594079	in-del	-/GTGTGTGTGGGTGC			intron-variant	Arhgap10	Mm_Celera	8:77347959	GCTCTGTGTGTGTGT[-/GTGTGTGTGGGTGC]GTGTGTGTGTGTGTG	78514
rs257629458	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77441657	TAAACTACTTGTGTT[A/C]AGATATTTCTAAAAC	78514
rs257640269	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77383206	TCTGTCTAACACAGG[A/G]ACAAAAGGTTTAAGA	78514
rs257641458	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77424351	ATGACCGCTGCAGGG[C/T]TTCCTGCAGAGAATG	78514
rs257646603	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77482467	AAAGAAATGAAAAGG[A/G]AAGAGAGGGAGAGGA	78514
rs257659845	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77338990	CAGCCTGATGGAGAC[A/T]GTTCCTCAGCTGTAA	78514
rs257662316	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77292859	TGCTTTGTCACTAGC[A/G]CTAGGGGGCTGAGCT	78514
rs257663696	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77308449	AGACCTAATACAGGT[G/T]CTCTTCAAACCATTG	78514
rs257670094	in-del	-/TT			intron-variant	Arhgap10	Mm_Celera	8:77465853	AATATAAAGTTGGAG[-/TT]TGGGGGGGGGGTCAG	78514
rs257682794	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77292759	AGATACTCCCCCCCC[-/AA]TTTGTTCTCCCAAGA	78514
rs257687145	in-del	-/TC			intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77483866	GTCACAACTTCAAGT[-/TC]GCTTCCTTCTCTCCG	78514
rs257692033	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77453622	AAAACCCTGACAGTT[C/T]CATCACTGAGAATGG	78514
rs257697101	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77497959	TAGCCTCTGGGCCAG[A/G]CTGTGAGGGTATATT	78514
rs257711162	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77271867	CCTATGATGTCACGA[A/C]CTCCGAGGAGCCTGG	78514
rs257716632	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77278160	ACACCGAAGGGATGG[C/T]GCTGAGCGGGGTCCT	78514
rs257724453	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77490168	TGATTCACATTCCAG[C/G]CTGTGCTGACCCAGG	78514
rs257744191	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77411484	CACACACGTGCACAC[A/G]CATGCACGCACACAC	78514
rs257749215	snp	A/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77365562	CTGAATCTGTGTTTT[A/G/T]AAAAAAGAGAGTTGC	78514
rs257749562	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77272238	ACTACCTGACCTACA[C/T]GCAGCTGGGTTTCAT	78514
rs257769017	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77252823	TTTCTTGGTGACCTT[C/G]AGCTTCCTATCTAAG	78514
rs257769644	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77423020	AAGTGCCGTCTTCAG[C/T]GCCTCTTCAAGCTCA	78514
rs257774082	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77428791	GAGGGCGTGGCCACC[A/T]ACCTCAGAAGAGATC	78514
rs257775742	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77271373	GTGATGAACAGCTAT[A/G]TGGAAGTGTAAGCTG	78514
rs257775763	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77510135	CCCCGGTCAGAAGAG[A/G]GTATTGGATCCCTTG	78514
rs257788784	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77320920	CACTGTGACAGTCAA[C/T]CCAGACTGCCAACGT	78514
rs257789647	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77369819	GGGATGCCCATCTTC[C/G]TGTCACCTGTTTACA	78514
rs257790319	in-del	-/AAG			intron-variant	Arhgap10	Mm_Celera	8:77380096	ACTGTGTTTTAGGAA[-/AAG]AAGTTAAGAAAAAAG	78514
rs257790831	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77265671	GGCTGGGGTTAGGGT[A/G]GCCATGACTGGTGCC	78514
rs257806788	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77359310	TATCTGTATGAGCCT[C/T]CACTTCAACCTTATA	78514
rs257810213	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77407015	TTCTGCAGTTAAGAG[C/T]GGCAGCTGCTTTCAC	78514
rs257816230	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77294376	CTTCCCTACTGTACT[G/T]AAGGCTCTGAGTTTA	78514
rs257818230	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77265537	TGCATCTGTTAGGAA[A/G]AGTCCAAAACAGACC	78514
rs257818244	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77509453	CAGAAGGTAAGCATC[A/G]AAAGGAGGAAGAAAT	78514
rs257829407	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77502821	CCACGGCCCAGCAGC[C/T]AGTGGTACCAAGCTC	78514
rs257835171	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77436205	GTTTCCATTATGACT[C/G]TGGTGTGACATCTCT	78514
rs257850178	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77315290	TTTATCCTTCCTGTA[C/T]ACCACAAGTAAAACT	78514
rs257854544	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77477547	AAATCTAAAAGGGCC[A/G]AGTTCCGTCATCTAA	78514
rs257871561	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77406216	TAAAAGAAGGAAAAA[G/T]TATAAAAGAAGTAAC	78514
rs257875789	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77356272	AGGACCCACACAACA[-/G]GTAAGAATCCTTTGT	78514
rs257877370	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77407467	AAGACAGACAGACAG[A/G]CAAATTAATTCATTT	78514
rs257877621	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77258687	GACCTCCACTGTCCA[C/T]ATCTACAGACTCAAC	78514
rs257879451	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77316160	GGGACTTTAGGACTA[A/G]AGGGAAGACAGGAGC	78514
rs257888698	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77437509	CACCCTGTCACAGAA[C/T]AAAGCGAAGTGGGTA	78514
rs257897105	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77381979	TAAAAAAAAAGGGGG[A/G]GGCCTTTAAGGAGGT	78514
rs257906568	snp	G/T			intron-variant, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77517307	AAGCAGCGTTAGGGC[G/T]CAGTAAAACCTGACT	78514
rs257906572	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77265841	TGAGGTGTGTGTGCT[A/C]AGCCCAGCTTGTCTA	78514
rs257906664	in-del	-/TAAA			intron-variant	Arhgap10	Mm_Celera	8:77477218	TAAGACATTAGGATT[-/TAAA]AAAAAAAAAAAGACC	78514
rs257912085	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77337370	AAACCTCTGAAGACT[A/T]CGCAGCTTTGTTTTA	78514
rs257927594	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77463817	AGTCAACAGGACTAA[C/T]GGGAGCGCCTTGCAT	78514
rs257931891	snp	A/G			synonymous-codon, intron-variant	Arhgap10	Mm_Celera	8:77382729	ATGACCGTTACCTCG[A/G]GTTTCAACGGCGCTG	78514
rs257941605	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77401120	AGTTATACATTAATT[A/G]TAATGGTTTTTCACT	78514
rs257942455	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77284186	AACAGTTCCAGGACT[C/T]ATCATGCCCAGCAGA	78514
rs257948092	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77444117	CTGCATCTTTTCTAA[C/T]TCTCTAGTCCAAACC	78514
rs257950274	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77385329	GCTCAGGCTGTAACA[A/T]GCTCTATAAGACACG	78514
rs257953532	snp	A/C			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77516271	CAAGCAAATAACCCA[A/C]TCATCAAAAAAGTGA	78514
rs257959420	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77370530	AGGAACAATGAGAAG[A/G]GGTGCACGGGAGGCT	78514
rs257976794	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77506900	AAGACTACCACGTCA[C/T]TTCAGGAGAAAATAA	78514
rs257983287	snp	A/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484840	GGCAGAGAAAATTAC[A/T]GGGAGCTCTGTCTAC	78514
rs257988582	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77375620	CATGAGGAGAAAGAA[A/G]TATTCATTAAAGGTC	78514
rs257989402	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77491617	GGGTGAGCTCTCCAG[C/G]ACTGTCCCAGCTAGC	78514
rs257997404	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77383320	TATTATTTTCATACT[G/T]TGAACTGAAACAGAT	78514
rs258006090	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77381974	AACATTAAAAAAAAA[-/G]GGGGGGGCCTTTAAG	78514
rs258021103	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77464298	GGGGTCTGTGGAGTG[C/T]GGATTCTGCCTAATG	78514
rs258048555	snp	A/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77277076	TCCTGGGATTTAATG[A/G/T]CTTGGGTCGTTACTG	78514
rs258057635	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77357015	GAAGCACCGCTTGCA[-/G]GGGGGCAGGGAGGAC	78514
rs258058229	in-del	-/TG			intron-variant	Arhgap10	Mm_Celera	8:77508682	AGTTCTCTGAGGTTT[-/TG]TTTTTTTTTTTTAAA	78514
rs258059149	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77376024	AGTTTTCTGTCTAAA[C/T]GCAGTCCCAGCACGA	78514
rs258063070	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77498417	CCACCCACCCTGAAG[G/T]TACCAGCACACACAC	78514
rs258065644	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77418417	CAGGGCCTGTGACAC[A/T]GGGTCTCAGGACAGG	78514
rs258080788	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77470561	CAACAGGGTGCGTGC[C/T]CACAGCCGGCTCTGC	78514
rs258092235	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77461385	GACCATGTAGAGAAG[C/G]CAGCCATGAAGGGGC	78514
rs258100010	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77386443	GTAAGAGCACTGACT[A/G]CTCTTCCGAAGGTCC	78514
rs258126131	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77504849	AACAGAGAGTTTTAC[A/T]CTCTGATCTTCAGGC	78514
rs258153321	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77365557	AGCACTGAATCTGTG[-/T]TTTTTAAAAAAGAGA	78514
rs258164055	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77290168	AAACACACTGGGGAA[C/T]GCTGATGAGGGAATC	78514
rs258176165	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77467742	GTAACTCTGGGAGAC[C/T]CATCTGTGCCATCTG	78514
rs258198033	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77258258	TGGTGATGAACAGCA[A/G]TGTGGAAGTGTAGGC	78514
rs258201217	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77511576	GCTTCATGTGGATGG[A/G]CAAACAGGCTACACT	78514
rs258204135	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77359411	TCCCTTTAGAAGAAG[A/G]GCTAGTGTTGTAAAG	78514
rs258215124	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77397466	TTGAACACTTATTAA[A/G]GTAGCTTGAGAAAAA	78514
rs258219376	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77351815	TGCCAGATAGCTTTA[C/T]ATACCAAAAGACGTA	78514
rs258226128	in-del	-/GCTATCTGACTCCC			intron-variant	Arhgap10	Mm_Celera	8:77412786	GCCCTTATACATGCA[-/GCTATCTGACTCCC]GCTTCTTTGTCACAA	78514
rs258232023	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77414879	ACATCCATTCATTCA[C/T]ACACTGATACACACA	78514
rs258232592	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77262273	TGATTTCTCTTCAGG[A/G]TCAGTTTCTCAAGGC	78514
rs258238892	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77253293	CTCCAGTGCTGGAAT[A/G]GTGTGAAGTGCTCCC	78514
rs258244036	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77352684	ACACACACACACACA[-/C]CCCAAATAATGCCAG	78514
rs258249036	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77258963	AACTTGGCTGTCACT[A/G]CCAAGGGATCCAGGG	78514
rs258250054	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77496717	AGTGCTTCCATGATA[C/T]TTTTCAAACCATGAC	78514
rs258257335	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77458479	TTATCAGTTCAGTTA[A/G]CACAGTTCTGGGTGT	78514
rs258263921	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77453092	TGGACAGAAATAAAT[A/G]TTCTAGAATGACATT	78514
rs258271857	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77252744	CTGTACTTCCATTTT[A/G]GAGGCAGGAGACACA	78514
rs258312151	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77318617	TAAAGTGATACATCT[C/T]GAAAGGTGACAGAAA	78514
rs258315311	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77423223	ACACTACCTAGGAAG[A/C]GTAAGAACAATAAGC	78514
rs258326481	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77464523	AACTTGCTTCACACA[C/G]ATAGTAGGCCTTCCA	78514
rs258331496	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77452776	GAGGGCTGGAGACAT[C/G]GCTTGGTGGTTAGGA	78514
rs258342691	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77263433	TTTTGTGCAGTTAAC[A/T]CACTCTGAGGGAGAG	78514
rs258344904	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77253586	GAACACAGAGAGCTC[G/T]GTTTCAGCTCTGAAA	78514
rs258364797	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77466280	CACATGCACTGGCAC[A/G]TGGGGAGAAGATGGA	78514
rs258367002	in-del	-/A			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519186	AGGCAAGGGGGAGGG[-/A]AAAACTGGAGACTGA	78514
rs258367601	snp	C/T			synonymous-codon	Arhgap10	Mm_Celera	8:77413502	CCTCCTCTTACTTTT[C/T]TCCTGGACGTACAGG	78514
rs258370547	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77471551	TATGCCCGAGCAGTC[A/G]GTGCTCTTAACCACT	78514
rs258384105	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77325041	AAGCAGAAGCATGGG[A/G]TTTTCATCTTATTTC	78514
rs258384171	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77361548	ATTAAAATTCTGCTA[-/T]TTTTGTTTTCTACAG	78514
rs258393947	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77332078	AGAGAGGATGATGAC[A/G]GCATCCGAGATGAAG	78514
rs258397204	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77456574	CTTCCTAAACCTGAC[C/T]AATGTGGGTCATCTC	78514
rs258406643	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77328152	TCTTACTCCTCAAAT[C/T]TAAAGCTTGCTGTGG	78514
rs258415124	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77364629	CCTGGCGTCCTCCAG[C/T]CTGCGATGCCAAGGA	78514
rs258432592	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77419419	TGGAACACATGAGGC[A/G]TGTCTCTGGTTGTTA	78514
rs258432724	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77399124	ATCTATGGCAGTGGC[G/T]CTCAGCCTGTGGGTC	78514
rs258435290	in-del	-/AAAA			intron-variant	Arhgap10	GRCm38.p3	8:77388338	TTCAATACACTTGTC[-/AAAA]AAAAAAAAAAAAAAC	78514
rs258439966	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77495570	CCTAAGAAAATGTAG[-/C]CAGGTGAGGTTCGCT	78514
rs258451368	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77366938	AACCTGTGTTTAATT[A/C]TTTTTTACCTTTATT	78514
rs258451919	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77462810	GAGGCCTGGCTTTTT[C/T]TTTCTCTCCTCATAG	78514
rs258455912	snp	G/T			intron-variant, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77517467	GAACGCGCCCGAACC[G/T]CCTGGGAGAGGAATG	78514
rs258465128	in-del	-/GGG			intron-variant	Arhgap10	Mm_Celera	8:77269132	TCACAGGAGACAGAA[-/GGG]ATTGGCTGTGCTCAC	78514
rs258481920	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77357236	TATATCTGCAAAAAA[A/C]TCTTTTTAGTATCAA	78514
rs258483584	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77322153	AAAGACCAGACTGGA[C/T]ATGCCTGGGAACAAA	78514
rs258484830	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77433332	AGGCAACGAATGGGG[C/T]GCAGGGGGAGGCCAA	78514
rs258490721	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77497123	TTTTCATGAGTGTGA[-/T]TTTTTTTTATATTTA	78514
rs258494019	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77280732	GGGATCCACCTGTCT[A/G]TGCTTGTTCTGTCCT	78514
rs258500927	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77426590	CACTCTCTGACTCAG[C/T]GCAGGACCAGGAAGA	78514
rs258506086	snp	A/G			intron-variant, synonymous-codon	Arhgap10	Mm_Celera	8:77476568	CAGAAGAAAACTGCT[A/G]GTCCATGGCTTCAGT	78514
rs258514164	in-del	-/TAAAAAGCTAGCTGG			intron-variant	Arhgap10	Mm_Celera	8:77500923	ACTAACATAAGCTGA[-/TAAAAAGCTAGCTGG]TAAAAAGCTATCAAA	78514
rs258531839	in-del	-/AGAT			intron-variant	Arhgap10	GRCm38.p3	8:77287184	GAAAAACAGTCTCTA[-/AGAT]CACAGTAGAAATCAA	78514
rs258534306	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77266552	TCTTTAGGGTGTTAG[C/T]GGTCTGTGTAAAAAG	78514
rs258541506	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77350913	TCTTAATTACCTAGC[A/G]TGAGTATCCCTCAAA	78514
rs258548068	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77440304	CGGGCCACCCTTGAC[G/T]GGCAGGGGGCCACCA	78514
rs258549033	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77358797	AGAAAGCCTTCGGGA[A/G]AGACAAAAGGATCTA	78514
rs258556536	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77396150	CAGCAAGTTCATTAT[C/T]ACTCAGTGAAAGAAG	78514
rs258560941	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77426757	TGAGCATAAAAGACA[A/C]ACTTTCAGCTGGGTG	78514
rs258561259	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77434373	AGCGAATTGACCCCC[A/T]CGACCAGGTTCTTAT	78514
rs258566976	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77481019	AAATGACAGCCCACT[A/G]CCCGCACTGACCGTC	78514
rs258574406	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77491753	CACAGCCCTGCAACA[A/T]CAAAACGGCACGGCC	78514
rs258586574	in-del	-/ACGC			intron-variant	Arhgap10	Mm_Celera	8:77374751	GAGGCTCACATGCAG[-/ACGC]ACAATTGTCCCTACT	78514
rs258604596	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77369567	ATCGTTCATTTTCCC[A/G]GACATGAATGCTCAC	78514
rs258605893	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77345487	CCTCCACAAATCACA[C/T]GCACATAGAAAAAAG	78514
rs258615788	snp	A/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77292988	TTTTTCTAACCCGTC[A/G/T]ATCCTATCACTGTAA	78514
rs258619300	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77336753	AACCAGGGCGGAGCT[G/T]CGTCCCGGGTGAGGA	78514
rs258620887	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77487427	TGTGTGTGCACACAT[A/G]TGCACATACCCACGG	78514
rs258630400	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77433783	TCCGAAATCAAATGT[A/G]GTTCCTTCTCCTCCC	78514
rs258632458	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77357984	ATTTGAACGTTTGGG[-/C]CCCCCGTGAATAGAG	78514
rs258643891	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77330489	TATTAGCACATTAAG[C/T]ACATATGACCTGATT	78514
rs258663596	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77447047	TTTTGTTTTGGTTTG[G/T]TTTGGTTTAAGGGGG	78514
rs258663968	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77452595	CCCAGACGTGGTGGC[A/G]CGTGCCTGTATCCCC	78514
rs258664967	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77362761	GATGCTGGATACCTT[A/T]TCAGAATGAAAGGAG	78514
rs258672528	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77438658	CTGCGCCCTTTCTGA[A/G]ACGATCAGAAGGCCA	78514
rs258685421	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77337216	GGGACTGACTTTCAG[C/T]ACTCCTGATGACAAA	78514
rs258686341	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77333111	CCTTTTAATTTTACA[-/T]TTTTTGTGTGTCTGT	78514
rs258692238	in-del	-/AA			upstream-variant-2KB, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77518300	GAGATCAGACGACTT[-/AA]AAGTCGGGGCGGGTG	78514
rs258692864	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77398113	GTGGAAGCCCTGGAG[A/T]GGACTCTCAACTCCC	78514
rs258694799	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77479820	CCAACCTTGGCCTTT[C/T]AAGTCACTGTGCAAG	78514
rs258695761	in-del	-/CCCT			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503916	AACAAAGAACCCCCC[-/CCCT]CCCAGCAGCTGTGAA	78514
rs258707715	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77330904	TGCAACCATTTTTTT[A/G]AGATTTGGTCTGGCA	78514
rs258717534	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77491312	AAATAAACAAAGATT[-/AA]AAAAAAAAAAAAAAA	78514
rs258724842	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77285670	CTGAGACTATTTGTC[A/G]TGCTGACTGTGGAAG	78514
rs258725596	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77452357	GAGACAGGGTTTCTC[A/T]GTGTAGCCCTGGCTG	78514
rs258727906	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77348571	TGCAAAAGGTACTAC[A/G]GTTTTCCTGTGGTCC	78514
rs258740529	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77445177	AAGCCCAAAGTCCCA[C/T]AAAAAAGATATTCAG	78514
rs258746154	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77417391	TAGCCAGATGGGGCT[A/G]GAAATAGCTTGCTTT	78514
rs258754083	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77384956	GCTTTACAGCATAGA[A/G]TTCCTACACCTGGAA	78514
rs258754160	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485621	CCTCCATTTCCACTT[A/G]GTCAACACCAGTTAA	78514
rs258767418	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77404311	GCAGCCTCTGAAAAC[G/T]ATTCATAACAGCAGC	78514
rs258769017	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77331629	AGGCAGGGCACATAA[A/G]ACAGCACCTACTCCT	78514
rs258774197	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77311719	CTGAAATAAAACACT[A/G]GAGCCATGGGCCTGA	78514
rs258781435	in-del	-/AAATA			intron-variant	Arhgap10	Mm_Celera	8:77326431	CGACAGTGTACTCAT[-/AAATA]AAATAAGTAAATAAA	78514
rs258787054	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77340917	CACGCACATGCATGC[A/G]CGTACACACACACCA	78514
rs258787459	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77460411	CAATATTAGCAAGAA[A/C]GAAACATTTTCCAAG	78514
rs258795574	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77288499	TCCAAGTTGCTCCCT[C/T]CCTGGTTGTACAACA	78514
rs258808890	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77312258	TGGCGAATGGGGAGC[A/G]GAAGAGTTGGGTGGA	78514
rs258808944	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77296003	CACTATTAGAAGGTA[A/T]GGTGCTGCTGGAGTA	78514
rs258812670	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77349288	TTCTTTTACAATAAG[-/A]AAAAAAAAAGATACA	78514
rs258814105	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77320789	TAAACGGCCCCTCCT[A/G]ATTTCTATGAATATC	78514
rs258815156	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77457821	CCAGTGCTGAGTACA[A/G]ACAGCACCTGACCAC	78514
rs258826637	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77319486	GTTGTTTCCTAATAA[A/G]TTACTGCTAATTGCT	78514
rs258830236	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77265645	CCTGTTCTCCAGAAA[C/T]GGTCAGGCAGGGCTG	78514
rs258834062	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77312414	GAAAAAACCAAGCAA[C/T]ATCCTGGGCCAGGAC	78514
rs258845356	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77458636	CGTCCCAGAGAGGAC[C/G]GTGATGAGGTTACCT	78514
rs258865529	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77505697	CCCCGAGACACAGTA[C/T]GTGTTTGGAGATGCA	78514
rs258873929	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493337	GAAAGGAAAAGAAAA[C/T]TCCATGCTGAATTCC	78514
rs258880192	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77334014	GATTATTCAAGAGCT[-/G]GGGAAGTACCAGAAA	78514
rs258883059	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77313011	ATGATGACTCAAAGA[C/T]TCCAGCTACCAACCA	78514
rs258895126	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77400253	CCTAGTGGCTCCTAG[-/T]TTTATGCTACCAGAT	78514
rs258897746	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77415721	AATCTCGAGGGACCC[G/T]GGAAGATGTGCTTTA	78514
rs258899665	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77323145	CACCAAGCTACCTGA[C/T]CTGGCAAGCAACTCT	78514
rs258926650	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77512546	AAAAGTTAAACTTGT[A/C]ATTTTATGAGCTTTT	78514
rs258938073	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77418305	AAGGAATGTGAGGAC[A/G]GCTGACCAGAGCCCC	78514
rs258941909	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77273020	GTGGTGATATCCAGA[C/T]GGAAATGGGGTCTTC	78514
rs258959427	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77401282	CTAGCACTTCTGGTG[C/T]AGGTGTCTACCCCAG	78514
rs258962579	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77261898	GAGATCGTGGTAGTG[A/G]TGGCTGAAGATGAGA	78514
rs258964249	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77408161	GAGAGAAAGGCTGCA[A/G]CTTACAATCATGTAA	78514
rs258972227	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77273408	CCAAGGAGTATGTTG[A/G]TCTGGACCATTAAAA	78514
rs258974343	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77512919	TGAGATTGGAATCTT[C/T]ATTCTTTTCGTTTAT	78514
rs258996113	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77353375	TGTGCGCAGGCAGGG[A/G]GACTGACACTGAAAC	78514
rs259013481	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77464678	ATAATTAAATAAATA[C/T]CCAACTCTGGTTTCT	78514
rs259013819	in-del	-/TG			intron-variant	Arhgap10	Mm_Celera	8:77382230	CACTCAGGAGGGACA[-/TG]TATACACACAGAAGA	78514
rs259039668	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77500022	ACGGTTGATGTGTGT[C/T]GACTGTGTGCCCCTA	78514
rs259054988	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77281463	CAGCAGAGAATAAGG[A/G]ATCTAAAATTTTCAA	78514
rs259067640	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77286657	TCTACCAAGAAGGGA[C/T]CAAACATTCAAACTT	78514
rs259096394	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77273839	AGAGGGACATCACAC[C/T]GTGAACCCCAAGATT	78514
rs259103526	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77499801	ATATTAGCTTTATGT[C/T]TAATAGAGTCCCTCA	78514
rs259127918	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77376280	CCACACATCAACCTT[C/G]CACTACAGGGACATG	78514
rs259131663	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77401922	GCAGTGACCGTCGTC[-/A]GTGGCCTCCTCCTCC	78514
rs259137602	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77378619	AAGATTTACTTATTT[A/G]TTTGGTTACTTATTT	78514
rs259149710	snp	A/C			utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250741	CTGACTCCAGCAACG[A/C]CAGTCACGCTCTGCT	78514
rs259155572	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77408941	GACTTACTACACACA[C/T]CAAACAGCTTTATCT	78514
rs259173685	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77373358	GGAACCTTGGATTCA[A/G]AAAAATCTAAAAACA	78514
rs259182532	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77436857	TTGCAGACAGCAGTG[A/G]AGGAACCACCGAGCT	78514
rs259193769	in-del	-/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485373	CACGAGAAACAGGCT[-/G]GGGGGGCTAGCAGAA	78514
rs259203150	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77379119	ACACATCACTCACAC[A/G]GAAACCATGGTTGTT	78514
rs259204044	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77371644	GTGACAACTCTATAC[A/G]TGCATGGAAAACATC	78514
rs259207509	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77448143	AAAAGAATGACTAAA[C/T]GCCAAAGGAAGTTGT	78514
rs259211803	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77326426	GACAGCGACAGTGTA[C/T]TCATAAATAAAATAA	78514
rs259222900	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77271434	GGTCCTGATGTTTGG[C/G]TATGGGGCTCTGTAG	78514
rs259226492	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77400196	TGACAGCCGACAGCC[C/T]GTCCATTCTCTAAAA	78514
rs259227410	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77441136	AAATGAAGGGAGTGG[C/T]CGGGGAAAGGAGAGG	78514
rs259231839	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77279155	TTTAGCTAAGCCACT[A/T]TTTCAATAGCCCTTC	78514
rs259236661	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77472729	AATGTACTATATGAT[A/G]ACACATGAATATATA	78514
rs259236977	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77412267	ATGGGTTAGTTCCCA[A/T]GAGAACAGTCTGTGT	78514
rs259248751	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77319099	AGAAACCCATTGGAC[A/T]TGCAAACTTTATATG	78514
rs259250764	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77409305	GAGGTGTGGCAACAA[C/T]GAAATGCTCCAAGTT	78514
rs259260045	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77367955	AGGAAGAATCACACC[A/G]CTCAACAGCGGTTTT	78514
rs259264268	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77298336	GATCTGAGAGGAGTT[A/G]AGGTTAAGAGAAAAC	78514
rs259288777	in-del	-/GCTGG			intron-variant	Arhgap10	GRCm38.p3	8:77387516	AGAGAGCGAGTACTT[-/GCTGG]GCACTGGTGATCATG	78514
rs259289538	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77447351	AGCTGCCTCCAAAGC[C/T]GAAGATTAAATCACA	78514
rs259289913	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77252888	TGTCCTGTCGGTGCT[A/G]GCCTATTTCACTTAG	78514
rs259299433	in-del	-/CTCA			intron-variant	Arhgap10	GRCm38.p3	8:77433415	GTCCCTTCTCTTGGC[-/CTCA]CACACACACACACAC	78514
rs259301858	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77480552	AGTGCTGGGATTAAA[-/A]GGCGTGCGCCACCAC	78514
rs259304872	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77385299	AACCCACCCTATGCA[C/T]GGCTCCTTATGCCTG	78514
rs259322990	snp	A/C/T			intron-variant	Arhgap10	Mm_Celera	8:77344062	ATAGAAATGTGCCTT[A/C/T]CTGTCTCTTTCTTTC	78514
rs259342961	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77499692	CCTTTCACAAGGGTC[A/C]CCTAAGGCCATCAGA	78514
rs259361918	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77385931	TGTGTTAGTACCACG[A/G]TAATTCTGCTCCTTG	78514
rs259363002	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77291252	AGTAGTGACCCCAAA[A/T]GCAGGAGAAATGTGA	78514
rs259365094	snp	C/T			intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77492531	GCAGCTCCGCCCACC[C/T]AATGACTCAAAGTAA	78514
rs259367895	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77414322	GGCATTTCTTGCAGC[A/C]AGGCTCAAAAATAAC	78514
rs259376317	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77396695	CTGGGCAAACGCTCA[A/C]TCACTGGCTGAACTG	78514
rs259378824	in-del	-/TTCA			intron-variant	Arhgap10	Mm_Celera	8:77460463	GCAGAAGAAGGAAGG[-/TTCA]GAACAGAGAAAATGT	78514
rs259393718	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77496042	TATTTTAAGAAGGAG[C/T]ACTCCTAGTATCTTC	78514
rs259398958	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77354338	GAACTAGCTGTCTCA[A/G]CCCCTCTCCCCCCAC	78514
rs259404719	in-del	-/AGACCCGGAAC			intron-variant	Arhgap10	Mm_Celera	8:77434183	CTAGTCATCCTAGAA[-/AGACCCGGAAC]AGACTATGTTGTATC	78514
rs259405382	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77254087	GAGCAGACACAGACA[C/T]AGAAGAGCCCACACT	78514
rs259407932	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77280865	TCACCTAAGCTAGTG[A/T]GTTCAGTGATTTCCA	78514
rs259409002	in-del	-/GG			intron-variant	Arhgap10	Mm_Celera	8:77412283	GAGAACAGTCTGTGT[-/GG]GGGGTGTGTGTGTGT	78514
rs259413478	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77346571	CTCTCACACAGCTTC[A/C]TGCATGCATGAGGCC	78514
rs259418839	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77421569	CAGAAGTTTATAAAA[A/C]CAAGTGTAGTATTTG	78514
rs259419900	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77293875	AATTAAAACTTTAAA[A/C]TACATCCAGCAAAAG	78514
rs259424190	in-del	-/GAA			intron-variant	Arhgap10	Mm_Celera	8:77417672	CAAGAGAATAAGATG[-/GAA]AAAAAAAAAAGAGAG	78514
rs259428220	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77499206	ACTTAAAATCACAGC[A/G]TGAAGGGAAGGGAGG	78514
rs259435356	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77380637	GGTGCAGGTGGGATA[C/T]GAATTAAAAAGCAGT	78514
rs259444636	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77254391	AGCAACCACATGGTG[C/G]CTCACAACCATCTGT	78514
rs259453741	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77325227	AGCTTCAAGGAGTCA[A/G]GAGGATAGCACAAAT	78514
rs259455746	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77507940	AAAGTAAAGCTGACC[G/T]TATCACGGTGACTTG	78514
rs259469599	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77270264	GATTTGAAATGCCAA[A/G]TAGTCGCCCCTGAGG	78514
rs259478197	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77339500	TTGATGGTCTCAGAG[C/T]TCTTTAGGATTTTCA	78514
rs259492320	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77361657	ACATGCTAAGAGCAC[A/C]GTTTCTCCAGGTTTC	78514
rs259499291	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77383996	TGTGTGTAAAAAGCT[C/T]AGCACCTCAGCACCT	78514
rs259516708	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77470904	TTCTGAGCTGCCGTG[C/T]GGGCTCTAGGAACTG	78514
rs259517863	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77416822	ATCTCTGGACTCCTC[A/T]GACTCCTGGAGTCAG	78514
rs259551809	in-del	-/TTTT			intron-variant, utr-variant-5-prime	Arhgap10	GRCm38.p3	8:77492098	TCAACGAACCCTACC[-/TTTT]TTTTTTTTTTTTAAT	78514
rs259556848	snp	C/G			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77515335	TTAAGTGACCTCATC[C/G]GCAGGTTTCCAAATT	78514
rs259558134	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77362202	CTTATCTATTTTAAT[C/T]GTAAACAGCAAAGGG	78514
rs259558569	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77366541	TTTTCTGAGGCAGGG[C/T]CTCTCTCTGATCCAA	78514
rs259559971	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77262197	GAACAGATACGGAAG[A/G]TACAAGCCTGTCCCT	78514
rs259562638	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77272028	CAGAAATCGCATTCT[A/G]CCGCATTGCTTCCTA	78514
rs259574838	in-del	-/TGAA			intron-variant	Arhgap10	Mm_Celera	8:77422419	ACAGTAAGCAAAAGC[-/TGAA]TGAATGAATGAATGA	78514
rs259579105	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77422616	ATGTAATCTTCTCCC[A/G]GAGCCAGTATGTGTT	78514
rs259582754	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77397922	GCAGCACCCACCACA[A/G]TCTAAGCTTCCTGAC	78514
rs259584043	in-del	-/CA			intron-variant	Arhgap10	Mm_Celera	8:77475922	ACTGGCCAGTGACAT[-/CA]CACATTGAAGGGGTT	78514
rs259585295	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77321603	GATTACACAGACACA[G/T]AGATATACTGCTAAC	78514
rs259595759	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77254835	TGTTCCTTGGAGACA[C/T]GCCTGCAGACTGAGC	78514
rs259599947	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77455628	ACGTCAATTAAGAAA[C/T]ACCTCTGTAAGATAG	78514
rs259600616	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77266078	CGGTAAGGACAGCTA[C/T]AAGGGATAGTAATCA	78514
rs259612607	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77465250	GAACTGTTGTAAGTA[C/T]TATGGGCTCAACTGG	78514
rs259663820	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77360456	TGCCACAACACCACA[A/T]GTATGAAGTCAATTA	78514
rs259666707	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77405146	CCAAGTCACACTAAG[G/T]GAGACAGCCCCAGCT	78514
rs259672596	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77359757	GGCATGCTGCTGCCC[-/T]TCTCCGTCTGGGCCA	78514
rs259681210	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77255337	CTGGCCACCCACACT[A/T]CAGTGCATCATGCTC	78514
rs259687521	in-del	-/C			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77503613	CTGTGGCTCCCCCAT[-/C]CCCCGAGGGGGCTCT	78514
rs259692021	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77370338	AAGAATAAGACTTTG[C/T]CATCTTCAGGAAAAA	78514
rs259703998	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77292215	CACTGTACTCCTTCA[C/T]AGGCAGGCTCACAGT	78514
rs259712155	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77474037	CCCAACCTGGCCTGT[A/C]TTAGATCTCTGTGCC	78514
rs259718719	snp	A/C			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484249	CCATGTCAGGGACTG[A/C]ACACGGGGCCTCACA	78514
rs259726293	snp	A/C			intron-variant, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77517186	AGGACTTTTGACGAT[A/C]TCAACTACAGGCAGA	78514
rs259728773	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77334656	AACCAGCTACCCAGA[A/G]CTCAGAAAGAACTAG	78514
rs259730403	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77353996	ACACCAAAGAAGCAC[A/G]GGAAATTTAGAAGGG	78514
rs259732193	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77361122	GATTCACACCTAAAA[C/T]ATGTTTAGAGTGTTC	78514
rs259773501	in-del	-/CC			intron-variant	Arhgap10	Mm_Celera	8:77507869	TCAGCTTAATTACCA[-/CC]CATATATCACAGAAG	78514
rs259779194	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77479913	CCTCCCTAATATGGC[G/T]AAATCTGATACCGAA	78514
rs259779215	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77473265	GCACCACAGTAAGTG[C/T]ACCCACACATTCACG	78514
rs259781077	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77491374	AGTACATTTACTCCA[A/C]GGTGCACCCTTCTGT	78514
rs259802077	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77338408	TGCATGCTTCGAGAA[C/T]GTATTCCCCTCCCTC	78514
rs259804428	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77449868	AGACTTGAAGTAAAC[C/T]GCTGAGAGCAACAGA	78514
rs259833774	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77368351	GTCTACATTCACCAG[A/G]TCAGAGGACACTAGA	78514
rs259867300	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77332928	GCATGAGGATTCAAT[C/T]GCCAACACTTAGAAA	78514
rs259868877	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77375169	GGAAAATTTCGACTA[A/G]CATAAATTAGAAGAG	78514
rs259869376	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77455045	TTTTCAAGAAATACT[G/T]AAGTTATAAGTATGG	78514
rs259871088	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77448685	AGGCTACCTGTGCAC[A/T]CTGCCGCATCCCTAG	78514
rs259894611	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77437213	CCCTGCCCACTTTGC[C/T]TTATTCTGATCCACA	78514
rs259902610	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77331104	TTTCCTTTCTGACTC[C/G]CACACATTCCAAAAG	78514
rs259909833	in-del	-/A			upstream-variant-2KB, downstream-variant-500B	Arhgap10, 0610038B21Rik	Mm_Celera	8:77518913	TCAAAGTGATTCTTT[-/A]AAAACGTTCCGACTG	78514
rs259933616	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77454498	GTCGCCTAGCAGTCA[C/T]AGTAAACTAAGATAC	78514
rs259933760	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77333542	TGTTCCTGATGAGAA[A/G]GACAGGGATCAGACG	78514
rs259942286	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77474237	TCCGTACGAAGTCAG[A/G]TTATTTGCTTCCGTT	78514
rs259946471	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77370308	AGCTCGCATACAGAG[C/T]TCTACTCAGGAATAA	78514
rs259956136	in-del	-/AG/AGT			intron-variant	Arhgap10	Mm_Celera	8:77460214	AGCATTATGGGAAAC[-/AG/AGT]TAAAAATGTGGGTGA	78514
rs259958468	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77339289	AAACTGAAATATCAC[A/G]TGAGGCTCAGGTCAA	78514
rs259958664	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77436458	AGTTCCTCCCACCCT[A/G]GAGATCAAAGGCTGA	78514
rs259975382	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77400855	TTTCTGTGTCAAGGC[C/T]GTGACTCCTGGCTTG	78514
rs259979875	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77404433	TTAGTTAGCATCAAC[A/C]CTGGCTGACTGCCTT	78514
rs259982298	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77406204	GAGACCCACCCCTAA[A/G]AGAAGGAAAAAGTAT	78514
rs259983755	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77421731	CCAAAACCCTTAATC[A/C]CGCTGAGCAGTTAAA	78514
rs260012156	in-del	-/TGGC			utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250908	CAGTAGGACCCCCCA[-/TGGC]CGGCCGGGAGCTACA	78514
rs260018914	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77305743	CTGAGAGAACTAGAC[C/T]CCCAGAAGTACTGAC	78514
rs260023068	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77356613	CGACTCAGGGCAAGC[A/T]AGAACTGCAAATATA	78514
rs260023878	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77339773	TTGCCTCTCACCCTT[A/G]CTCCCAACGGGAAGG	78514
rs260025560	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77305408	TAATAAAAATGTAGG[A/G]AAAAAACTGAAATGA	78514
rs260030295	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77443320	ATAAGCAACGTTCAA[C/T]AAGAGTTGTATGGTC	78514
rs260034981	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77312401	GATGTTACCAGAAGA[A/G]AAAACCAAGCAACAT	78514
rs260044350	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77488270	CAGTGGGCCTGTGTT[G/T]AGATGGAGTCTAGGT	78514
rs260044912	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77315454	GGCTTCCCATTGGTT[G/T]TGGTTCATTAAAATT	78514
rs260052313	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77415247	CCAGGCTGATCTATT[C/G]TACCCGTCCCTGACC	78514
rs260061523	in-del	-/CACTCA			intron-variant	Arhgap10	GRCm38.p3	8:77433414	GTCCCTTCTCTTGGC[-/CACTCA]CTCACACACACACAC	78514
rs260062574	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77398805	CCTTCATGACTTGTG[C/T]CATCTAGAAAAACTG	78514
rs260070511	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77345131	CACAGGGAAGTCCCC[A/G]AGACAGTGAGCTCTC	78514
rs260076281	in-del	-/CACCACAGACCTGGGCTAACCACAGACCTGGGCTAACG			intron-variant	Arhgap10	Mm_Celera	8:77373429	CACAGACCTGGGCTA[lengthTooLong]ACCACAGACCTGGGC	78514
rs260081155	in-del	-/CACACACACACCC			intron-variant	Arhgap10	Mm_Celera	8:77352683	ACACACACACACACA[-/CACACACACACCC]CCCCAAATAATGCCA	78514
rs260087834	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77442659	CTGATGAGACAGGAG[A/C]GTCACACATGACAAT	78514
rs260099727	in-del	-/CCATTC			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485089	TCCCCTCAGCTTCTA[-/CCATTC]CCAGTCACTCACTTC	78514
rs260111394	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77306393	AAGACAAAACCTAAG[A/G]ATAATATATATAGAA	78514
rs260131203	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77315566	CTTCTGTACCCTTCA[C/T]TCGTCAATGCCAAAC	78514
rs260131319	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77321732	CTATGGAGATGTCCA[A/T]TTACCCTGATTACAA	78514
rs260134537	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77463501	ATGTTGTGAGCTGCC[A/G]TGTTGGTACTGGGAA	78514
rs260148430	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77428460	TAAGACCCACAACTC[A/G]AATCAATGGACCTCT	78514
rs260148471	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77460674	TATCTCCTGTAACTT[A/G]TGATTGCTCCCCTTG	78514
rs260155783	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77296775	TGACTTCTGTGATAA[C/T]GCTAAAGAATATTGT	78514
rs260157153	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77371205	TGGTTAAAGGCACAC[A/G]GCCAGGAAGCCCAAC	78514
rs260161045	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77275339	CCAAGTTAGGTATTG[G/T]TCCTCCTTGTCTGCT	78514
rs260165789	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77252007	AGGCAACCATTTGTT[C/T]TCCCCGTTGCGAGAA	78514
rs260170909	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77426735	CAAGAAGAAAAACAG[A/G]AAAGGCTGAGCATAA	78514
rs260186724	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77325965	CCTTTCCAGCCCGTG[C/G]TCACTGCTCTTCTTT	78514
rs260190022	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77409954	GCAAAGTCCACACCT[A/G]GGATTCTCTGAAATA	78514
rs260191342	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77316136	CCTCCTATCACAGGA[A/G]ACCGGAGAGGGACTT	78514
rs260191893	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77470805	TGTATGGACCTAAGT[G/T]TATTTCATTATACCA	78514
rs260201358	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77271063	GTGAGAGTATCCTGG[C/T]TGGTTTTGTGTGTCA	78514
rs260209772	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77435877	AAAAGCAACATTTAA[C/T]TAGGGCAGGCTTATA	78514
rs260213614	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77375002	CAGAATTGGACTGAG[-/C]CCCATCCTAATCCTC	78514
rs260220762	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77469794	ATTTTCAAGCACATC[C/T]GTTTTTGTCTTGGGT	78514
rs260233666	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77429761	ATCTCTGCTCAGCTC[C/T]CCACACCACTTCTGC	78514
rs260238311	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77514675	GCTGACCTGGCTCTC[C/G]CTCCAGCCGCTCCAC	78514
rs260248080	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77410142	CAGGCTCAAAGCCAA[G/T]GCTACAACTCCTCCT	78514
rs260252287	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77329859	GAGCACAGATGTGGT[A/T]CACAGATAAATATGC	78514
rs260256614	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77482922	AGATGAATCACAAGC[C/T]ATCAATAATATTTTA	78514
rs260271467	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77273499	ATTTCACACAAAAAC[A/G]TGACTAGAAGCTGGG	78514
rs260273863	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77418778	TCAAAGGGCCCTTTC[A/T]CAGGGTTGCCTAAGA	78514
rs260275746	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77435346	GATTGGAGGAGACAC[A/T]TCTGCAAGCTATGTG	78514
rs260276928	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77431925	ggggagaggagtggg[A/G]ggggaggggagggga	78514
rs260281807	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77272736	CCATTCCAGTGGTTT[-/C]CTACAAACCACTGTT	78514
rs260290762	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77265142	TATTAGAAGCGACTA[C/T]GCCCTGTAGTCTCAG	78514
rs260295441	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77346209	CACCCTTGGGGATAC[A/T]CGGTCCAGCCAAGAA	78514
rs260300624	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77426556	GGCGCGAATCATGGC[A/G]GAGCTTCTGAGACAG	78514
rs260329418	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77469603	AGCAGTTAAGCGCAC[A/T]AGCTCCCGAGTTCAA	78514
rs260335552	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77290627	TTCCCTAATGCTATG[A/G]CCCTTTAACACCTCA	78514
rs260337204	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77513360	AGGAAAGGAGTCTCC[G/T]GGGTCCACGAGAGCA	78514
rs260349094	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77425242	TATAAATAACTGTTA[C/T]TAGTCAAGCCTAGGA	78514
rs260349356	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77388077	CAGCAGCACACAGAA[A/G]AGAAATCAGTGCTGG	78514
rs260352650	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77475810	AAAGATAACTACTGG[A/T]GCTCTCGGGCAAATT	78514
rs260354454	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77268829	TTTCCAGTCCCTTGG[C/T]CCTCCTCGGGATGGT	78514
rs260373962	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77330851	ACAGAACTGTTCTCA[C/T]TTACAAAGGAGTATA	78514
rs260396730	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77381632	GATCAAATACATGAC[A/G]CAGAGGTATAAAATC	78514
rs260399884	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77475395	TTGTCTTTTATCTGA[A/G]AACTAAATGATCAAC	78514
rs260401364	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77481606	CAGAGCACACATCTC[A/T]GACGTCAGAGGCCTG	78514
rs260404285	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77282746	CTAGACCAAGTTCTA[C/T]CGCAGCCAGTAACTT	78514
rs260422343	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77378805	TAGGCAAGGAATGAA[A/G]GCTTGGGTAAAATGG	78514
rs260431741	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77283808	TGTAAGAGCCAGGGA[A/T]TGTGGCCCAGGAGGG	78514
rs260435878	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77446466	CGCTGGCCTTGCAAC[C/T]TTTATTAATTCCATT	78514
rs260446076	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77301882	TACAGGCCTTTCCAC[C/G]GGTCTTGAACCCGAG	78514
rs260447398	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77481103	TGGCCCACTGTCCAC[A/G]CTGACTGTCTACACA	78514
rs260447793	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77334379	AATACAGTGGAGTCC[A/G]TGGAGAGCAGTGCAG	78514
rs260453778	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77459747	GGCAAGCCTCTCTGA[A/G]ATGCTCTCACAGATG	78514
rs260454968	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77505592	TCTACATGGAGTTGC[-/G]GGGGCCAGCGGTGTC	78514
rs260460552	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77486499	ACTAAACCTAGACAG[A/T]GACAGCAACTTTTGA	78514
rs260460687	snp	C/G			synonymous-codon	Arhgap10	Mm_Celera	8:77250925	GGCCGGGAGCTACAG[C/G]AGCTTGACATAATTC	78514
rs260463187	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77398677	TAAGACTACAGACAA[A/G]GCTCTGAGACAGCTT	78514
rs260481776	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77410662	CGTGCCTAACTGAAT[-/G]GAAAGGGGATTGATT	78514
rs260486512	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77501934	GGGACGGATCCTAGT[A/G]GCAGATCTTCAAGAG	78514
rs260489317	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77349495	AGAATCACACCCGGG[A/G]CAGCAACAAAGGCTG	78514
rs260489552	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77363275	TTTTGGAAAGGAAGG[A/G]AGAGGGGGAGAAGGG	78514
rs260517599	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77296341	AACCACACGGTGGCT[C/T]ACAACCATCTGTAAT	78514
rs260530729	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77251857	ATTTTATACTAGAAA[C/T]ACATACACCCCTGGT	78514
rs260549390	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77501490	TACGACTGCCACAGC[A/G]GATGAAGAAGACGAA	78514
rs260552819	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77357079	GTACAGGAATTATCA[A/T]TATCATCTAAACCCT	78514
rs260556848	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77420458	TGGGGACAGGGGTCA[C/T]GGTATGGCGGGGGGG	78514
rs260557026	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77256196	GGAGGTAGCTGTCTC[A/C]GACAGTACAATGCAA	78514
rs260585048	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77463265	ACCTGCTCAATCTGT[C/T]CACTCAACCAGCTTA	78514
rs260585670	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77256931	AACTGCAAAGCACAG[C/G]GATGGTGCCAGAGAG	78514
rs260595303	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77428889	AAATCAAAGGAATAT[A/G]AACATAACTGTACAT	78514
rs260614467	in-del	-/GGTG			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503840	ATTCCACCCAACTAT[-/GGTG]GGTGGCCTAGAGTTT	78514
rs260620919	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77323828	TCCACTTCTATATTT[C/T]CACTTCCCAAAGTTT	78514
rs260621664	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77471971	TAAACCAGATCACTT[A/G]GCCACCCAACAAGTG	78514
rs260624720	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77443900	AGAAAGAAAGGAAAA[A/G]AGTTATAGTTTAGAA	78514
rs260625144	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77387337	CCTGGCGTTACAAGG[C/T]GGTTATAATAAGCAG	78514
rs260629234	snp	A/T			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77516935	ACTGAGGTGGCCAGC[A/T]TCGAGCATGAAGAGT	78514
rs260647616	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77377944	GCATGAAAGCATACA[G/T]ACAAACTCCTGTCAC	78514
rs260654692	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77268604	GGATAGAGTTATCAA[A/G]ACCACCAGAGCAAGG	78514
rs260658714	in-del	-/ACAA			intron-variant	Arhgap10	Mm_Celera	8:77315402	TCATAATGGGGGCTG[-/ACAA]ACAAACACCAGTCAG	78514
rs260665292	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77418586	CACCACACTGAGTAT[A/C]AATACCCACCATCTT	78514
rs260669345	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77374721	TCACATGCAGACAAT[G/T]GTCCCTACTGCAACT	78514
rs260670455	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77333449	CATTCATTTGAAACC[G/T]AAAATGACCTCTGGG	78514
rs260701293	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77278117	TTATCAACATTCCAG[A/T]CGTGAAGGAGTTCCC	78514
rs260734383	in-del	-/ATAAATAAATAAATAAATAA			intron-variant	Arhgap10	GRCm38.p3	8:77320342	CTGTCTCAAAAATCC[-/ATAAATAAATAAATAAATAA]ATAAATAAATAAATA	78514
rs260738728	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77467820	TTAATCCGCATCAGA[A/G]CTGAGAACTTTCTCA	78514
rs260740841	in-del	-/CGCACACACACA			intron-variant	Arhgap10	GRCm38.p3	8:77385233	CGGGAGCTCCTCGAG[-/CGCACACACACA]CACACACACACACAC	78514
rs260747930	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77356361	CAGGGCACACAGGCA[C/T]CCATGAGGTAAAACA	78514
rs260754082	in-del	-/TCTAAGGGC			intron-variant	Arhgap10	Mm_Celera	8:77345708	TACAAGAGATGGCCA[-/TCTAAGGGC]TCACAGCCCAACACA	78514
rs260754523	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77287437	TCAAATGTTACCCAT[-/G]ACATATAGAGGGTGA	78514
rs260759360	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77315389	CAATCAAGTAGACTT[C/G]ATAATGGGGGCTGAC	78514
rs260769480	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77432390	AGGTTCCAGGGCTTC[A/G]GGTGGGAGGAGTGTC	78514
rs260770602	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77362861	CATTAGTAACAAACT[A/G]ACTCAGCGTGGCATT	78514
rs260779736	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77382075	CACACACACACACAC[A/T]CACACTCACACACAC	78514
rs260793613	in-del	-/AAGACT			intron-variant	Arhgap10	Mm_Celera	8:77396498	GAGTTATGGAAAGAA[-/AAGACT]AAGACTAAAATTAAA	78514
rs260796565	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77353099	TCAAGTCAAAGGCAG[C/T]ACATTCTTTGATTTC	78514
rs260797816	in-del	-/A			intron-variant	Arhgap10	GRCm38.p3	8:77286216	TCATGTAGCAAGAAG[-/A]AAAAAAAGACCTGCA	78514
rs260800294	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77446379	TGATTCCATCCGATG[C/T]TCGTGCATCACAAGA	78514
rs260813510	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77379584	TTTCAGTACTGACTG[A/C]CCCTCTGTGTTTCCT	78514
rs260825422	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77305910	GTATTCACACCACAG[C/T]GAGCCCTGGATACTC	78514
rs260826771	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77480667	CAGTACTGACAAAGG[C/T]CAGAAGAGGGAATCA	78514
rs260844285	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77253559	TCCATGACAAATGGC[C/T]TTGGCACAAGAGAAC	78514
rs260849050	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77451253	TCAGTAAGGTCTGGG[C/T]GGCCAGCCGGGGACT	78514
rs260850821	in-del	-/TGCTGT			intron-variant	Arhgap10	Mm_Celera	8:77384015	ACCTCAGCACCTCCC[-/TGCTGT]TGCTGCTGCTGCTGC	78514
rs260851656	in-del	-/CCC			intron-variant	Arhgap10	Mm_Celera	8:77385472	CCTTCCAGATCTGCA[-/CCC]CCAACTTGTAAGATC	78514
rs260855666	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77452245	TAATGCAGAGATGAT[A/G]GACGGATTTGTCTTC	78514
rs260859505	in-del	-/TG			intron-variant	Arhgap10	Mm_Celera	8:77321750	CCCTGATTACAACCA[-/TG]TGTGTGTGTGACCCT	78514
rs260860308	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77341391	GGAAATCATGGCCTC[C/T]GACGCAGAGGAACTT	78514
rs260868971	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493812	TCCTGTAGCCAGGGG[A/G]GTGAGACAGTGAAAT	78514
rs260872703	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77422711	CTGAGACCCACAAGG[C/T]GGGAGCAGCAGCTTC	78514
rs260882803	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77329603	GTCCTTCATCTTTTT[A/T]AAATTTAATTTTGTT	78514
rs260894296	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77273355	ATCTAAAGCAGGAAA[C/T]CTAAGTGTGCAGGAG	78514
rs260901104	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77465852	CAAATATAAAGTTGG[A/G]GTGGGGGGGGGGTCA	78514
rs260906004	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77451513	CAGACCCATCGCCTC[C/T]ATTTTCCATGGCAGG	78514
rs260909523	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77444345	CATGTCCTGTCAGGC[C/T]ACACAGAACATCACA	78514
rs260913895	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77342005	GCTCAGTCATATTAT[A/T]CCACACCTCAGCCTC	78514
rs260913988	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77335599	AGATACCATGTGTAG[C/T]CCAGTGGTGACTAGC	78514
rs260925992	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77402955	AATCCTATGAACTTA[C/T]AGAAGTAACATGCCC	78514
rs260951078	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77354810	TTTACCCAAGCTGGT[A/G]TTTTCTTCCCTATGA	78514
rs260955215	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77450216	TGAGTTCACGAGGTA[C/T]GGAGCAAAGCGCCAG	78514
rs260957629	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77362287	CGGAATTCAAGCCTT[-/G]GGGAATCACTACAAA	78514
rs260959909	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77335945	GAGCATCCCCAAACA[A/G]AAAATTTGAATATAA	78514
rs260968571	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77271204	CCCCTTGTGGGTGGT[A/G]CTATCCCTGGGCTGG	78514
rs260975071	in-del	-/TA			intron-variant	Arhgap10	Mm_Celera	8:77259861	AATAAATAAATCTTT[-/TA]AAAAAAAAAGCTAAT	78514
rs260978757	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77310101	AACCACATGACCACG[A/G]ATCACCAATCGACTT	78514
rs260980074	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77491846	CATGCCCTCACCCCC[C/G]GCCCCCGACAGCAGC	78514
rs260987826	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77310969	CCAGCCACAGTAGAC[-/T]TTGGGGTTCATTAGT	78514
rs260994870	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77446524	AATCAGTCACTGCAT[-/G]GGGGTAATGCATGCC	78514
rs261001113	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77317312	CCAGAAAACAAATCC[A/G]GAAGTAGCTGGCGTC	78514
rs261001798	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77347508	GAAATCCACCTGTCT[C/T]TGCCTCCCAAGTGCT	78514
rs261004137	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77408525	TTCGGACCTGGGAGG[C/T]GTGGTGAGGATCAAG	78514
rs261007726	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77294654	CACCAGGCCTTCCTC[C/T]AGCTGCCTCTCCCTC	78514
rs261024366	snp	C/T			utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250667	GGTCTGCCCTCTCTC[C/T]GTTCCACAGGTGGGA	78514
rs261032385	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77466120	ATTGAGATAACTCAT[-/A]AAAAAATGTTTAATC	78514
rs261044832	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77412505	AACTCACAGAGATCC[A/G]CCTGCCTCTGCCTCC	78514
rs261046704	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77406125	CAAGAAAATCTCTGG[A/G]GCCAGCTTCGTCTAC	78514
rs261050554	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77318038	TGTCTGCTGACCATG[A/G]GGGCAGCTGCCTCAG	78514
rs261072738	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77359347	TCGCTGCCCAGAAAA[C/T]TAGCAAACTATCTTT	78514
rs261089762	in-del	-/CACAC			intron-variant	Arhgap10	Mm_Celera	8:77395802	AATACATAATGACAG[-/CACAC]CACACTGACTGGAAT	78514
rs261099932	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77473559	GCGAGGTCATAATGC[C/T]TGCAGGCTGCCAAGG	78514
rs261114146	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77272565	CCAGCCCAGGGGCTG[A/G]GCTGCCCTTCCCCCA	78514
rs261127822	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77447985	CACACCTTATAATAG[C/T]GCCACTCTCTATGGG	78514
rs261128708	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77345018	TCCCTGCTCTCCAGT[-/C]CTTCCTTCTCCTTCT	78514
rs261129859	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77340642	AATGTATGCCTCTAC[A/G]TGCTGTTGCACACCC	78514
rs261131738	in-del	-/TTT			intron-variant, cds-indel	Arhgap10	GRCm38.p3	8:77492099	TCAACGAACCCTACC[-/TTT]TTTTTTTTTAATGAC	78514
rs261135708	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77382001	TAAGGAGGTGGTTAG[A/G]GTATTAGAGTAAGTT	78514
rs261139585	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77431327	TTTGTGCATGGCTCT[C/G]TTAGAAGAGACCACT	78514
rs261150054	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77279104	AAGTCTTGTCCTGCC[A/C]TCCACACAAATCCTA	78514
rs261150261	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77489899	ACTACCAAATTGGTC[A/G]GACCAAATAATTTAT	78514
rs261161019	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77459610	ACTCACTCCTACCTC[A/G]GTCTCCTGGGAGCTG	78514
rs261164214	in-del	-/CAGAGCATTCTA			intron-variant	Arhgap10	Mm_Celera	8:77507723	CCCTGTTGCCTACGG[-/CAGAGCATTCTA]CACCGCAGCAGAAAG	78514
rs261171566	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77412073	GAACTTTGAACGAGC[C/T]TTGGTTTCTTTAATT	78514
rs261171754	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77350361	AATTTAATTTCTATC[-/T]TTTTGTTTGCCAAAA	78514
rs261178627	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77453725	CACAACTGGCCATGT[A/G]GCATAGGGCCTAAAG	78514
rs261180466	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77279585	GTTCCTTCTCCTGCA[A/G]ATACGTTTGTGTGTT	78514
rs261183839	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77438962	CTAACCTAAATTCAC[G/T]AAAACCAGTGAGTAT	78514
rs261184548	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77375941	TCCGATTTTGGTGTC[A/G]ACACACAAAATCAAG	78514
rs261188104	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77430842	AGGTCAGCACACAGG[A/G]AGAGGAGAGGAGAGG	78514
rs261199817	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77497027	ACAGAGTGAGTTCCA[A/G]GACAGCCAGGGCTAC	78514
rs261218609	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77322967	TGCATTAAGCTCCAG[A/G]GAGCAAAGAGGAAGA	78514
rs261222707	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77422125	AACGAGGCCTGCTCC[A/G]GGGTCATGGAGGCAC	78514
rs261226999	in-del	-/CC			intron-variant	Arhgap10	GRCm38.p3	8:77491835	ATGGACTCAGACATG[-/CC]CTCACCCCCGGCCCC	78514
rs261227173	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77376875	CTTCTGGGAAAATTC[A/G]TCCTGGGCCCCCACA	78514
rs261228174	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77275782	TTATGAGCAAACTTC[C/T]CATGCTGTCCTTGTG	78514
rs261230014	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77295779	TCAAAATCACTCTAT[-/A]AGCCAAGCTCATAGC	78514
rs261232420	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77438344	AGATCCGTTACAGGA[C/T]GTCATTTCTCTGGGG	78514
rs261246658	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77332866	AGTAGTGTTTGCCAT[C/T]GCAAACACTATTAGG	78514
rs261249248	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77372131	TCTTTCAGGGTGGAC[-/A]GCCCCAGGGCTCACT	78514
rs261254847	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77276985	CCCGTCCCCTTCCAG[C/G]CAGGAAACAGAAAGG	78514
rs261266083	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77404981	GAGCGAGCCTGGACT[C/T]ACACTGAGACACAAA	78514
rs261266577	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77316937	TCCTCAATAGAACTT[A/G]CTGACATGTAAGTAA	78514
rs261267399	in-del	-/A			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485715	CAAGTCCATTGTCAG[-/A]AAAAAAAGAGGCAGC	78514
rs261269651	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77408110	TTATACATAAAGGTG[A/G]TTTAGCAGTAACCCC	78514
rs261271713	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77428309	ACTAAACCAAGCGAA[A/G]ATTAAATATTACTCA	78514
rs261281793	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77357540	TCAAACCTCAAAGAG[C/T]CACGGCAGAGAAGCG	78514
rs261287536	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77452513	AAACGTTCTCAGTCA[A/G]AACACACTGGGCCAG	78514
rs261296013	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77326879	TTCTTGAGCTTCATA[C/T]GGTCTGTGAGTTGTA	78514
rs261297592	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77471438	ACAATATGAACTAAC[C/T]AGTACCCGGGAGCTC	78514
rs261306658	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77496600	AGACAAATTGCCTTA[-/T]TTTTTTAAAAAATGT	78514
rs261308748	in-del	-/CGCA			intron-variant	Arhgap10	Mm_Celera	8:77448160	CCAAAGGAAGTTGTG[-/CGCA]TGCGCGCGCGCACAC	78514
rs261311057	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77396787	AATCATGCATCACAG[A/T]GAGCCTTGCTAAACA	78514
rs261311090	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77383545	GTTCAGAATATGCAT[C/T]ACTATGCTGAAAGTG	78514
rs261322306	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77516084	GAATAGGTACACGTA[C/T]GTCCTCATCTACTGA	78514
rs261324372	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77495573	TAAGAAAATGTAGCA[A/G]GTGAGGTTCGCTGGA	78514
rs261327027	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77271864	TGACCTATGATGTCA[C/T]GAACTCCGAGGAGCC	78514
rs261331929	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77257590	CTTTCAAGGAAATGA[C/T]GGGTTTCTGAAGCAA	78514
rs261334266	in-del	-/AACAA			intron-variant	Arhgap10	Mm_Celera	8:77290207	TATAATCAAGTCCAT[-/AACAA]AACAAAACAAAACAA	78514
rs261354349	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77297726	ACAACAGTGGTTTGG[A/G]AGGGTTTTGTCTCAC	78514
rs261354777	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77280684	GGCCTGAAATTGCAC[-/A]AAAAAGTCTATGCTG	78514
rs261355121	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77500466	TACATGCTTAAAAGG[-/T]GTGGACAGGCCAGAT	78514
rs261359953	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77383989	CATGTGCTGTGTGTA[A/C]AAAGCTCAGCACCTC	78514
rs261378043	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77491098	AAGAAGAAATAAAAA[A/T]AAAAACTAAGGGGCT	78514
rs261391608	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77253263	CACCAACGATTAGTT[C/T]CCCCTTGCTCCCTTC	78514
rs261403627	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77252631	TTCAGAGATATCTGT[A/T]CATTTTCTTATGCCT	78514
rs261420573	in-del	-/AGAA			intron-variant	Arhgap10	Mm_Celera	8:77506619	CAGGCAGACACTACC[-/AGAA]AAAAAAAAAAAAACA	78514
rs261423574	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77514605	TTGTGAACCACCTAA[C/T]ATGGGTGCTAGGAAT	78514
rs261433132	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77330811	GTGTGGTTCTGGTGT[A/G]CACTGTTTCTTTATG	78514
rs261440847	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77430102	TTGGTCCCAGGCTGA[A/G]GTGAGAAGTGATAGT	78514
rs261444245	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77476217	GCCTTTTCTCTTATA[C/T]AGAGTGTGCTATCAC	78514
rs261446889	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77366710	GCCATCACTCCCACA[C/T]GATCGTTTCCTTTTT	78514
rs261447069	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77504640	CACGGGGCGAGCATG[A/G]CACACTGGCCAGCAT	78514
rs261455856	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77417818	CGTGGGGCTCACACT[A/C]GTGCTCTACAGCAGC	78514
rs261465683	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77274158	CCCAGTATATGGCTC[C/T]TGAGTCTTCCTTGGT	78514
rs261469535	in-del	-/AAAC			intron-variant	Arhgap10	Mm_Celera	8:77286914	CACAGTTAAAAAAAA[-/AAAC]CCAAAATAACAATAG	78514
rs261488541	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77382705	CATGAATAAAGCTGC[A/G]GGCAGAGCATGACCG	78514
rs261498440	snp	C/G			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77504280	TACAGTCTGGGGGGG[C/G]GGGGGGAGCAAAACA	78514
rs261501749	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77254620	TGTGATTATTCTAAA[A/G]CCCTAACTAGGAACA	78514
rs261503074	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77259581	ACCCTTGCTTCCCAA[A/G]GTTGCCTTATTGTTG	78514
rs261503171	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77323427	CTTCCAGAAGTTTTA[C/T]CAACTCCCGTGGCAC	78514
rs261503238	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77266173	GCCATGCTGACCGTG[A/G]GCTTGTGTGTGGTTT	78514
rs261529823	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77499827	CCTCACCAGATGAGG[A/G]ACTGTATTAAAGACT	78514
rs261530714	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77260203	AGAAAGTCACACAAG[C/T]TTAAACACTGAGCAC	78514
rs261535412	in-del	-/TAAA			intron-variant	Arhgap10	Mm_Celera	8:77464668	TTGCTAAAATATAAT[-/TAAA]TAAATATCCAACTCT	78514
rs261541654	snp	A/G			missense	Arhgap10	GRCm38.p3	8:77409596	CTGTCCGTGGAGTCC[A/G]TGTGCCTTTTGGTGC	78514
rs261546985	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77422802	TCAACACCAGGCACG[A/C]TGCTGCAACAGCCCT	78514
rs261571243	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77396370	ATAGTCAACAACGCA[A/G]TGGTAAGAAACCTCT	78514
rs261586403	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77509586	GGGGGATAAAGAATT[C/T]TGAATGGAGGTTTAT	78514
rs261599641	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77405637	TTCTCCCAGAAACCA[C/G]TACATACTAATAACA	78514
rs261607014	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77452434	ATCCGTCTGCCTCTG[C/T]CTCCCGAGTGCTGGG	78514
rs261617611	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77358744	TCTTTTAATGACAGC[A/G]CAAGCTATGCTCTAT	78514
rs261623317	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77386357	GGCTGGTCTTGAACT[C/T]GGATACTAACTCCAC	78514
rs261623371	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494987	TTTAACTGTATATTC[A/G]AAACCAGTAACAAAG	78514
rs261627938	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77314744	GGACTCAGTCAGAAG[A/C]AGACACGGCTCTGCC	78514
rs261646912	in-del	-/GTGA			intron-variant	Arhgap10	Mm_Celera	8:77424944	ATGTTTGTGTGGTGT[-/GTGA]GTGTGTGTGTGTTCT	78514
rs261655079	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77380886	CAGAAGGGAACACGG[C/G]AGAAATCAAAAGTCT	78514
rs261659108	in-del	-/ACACACACAC			intron-variant	Arhgap10	Mm_Celera	8:77489514	CACACACACACACAA[-/ACACACACAC]ACACACACACACACA	78514
rs261664222	in-del	-/AG			intron-variant	Arhgap10	Mm_Celera	8:77255319	GCCAACATGCTAGAC[-/AG]AGCTGGCCACCCACA	78514
rs261673524	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77376589	GACACCTCTAGCTCT[-/C]CAGCAGCTCCTCCCA	78514
rs261678464	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77282012	TTGCAGGGAGCAACG[C/T]GATCCTGAGATTGAA	78514
rs261685161	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77451172	CCTCTCTCCTCAATC[A/T]GGTCAGAATGTATTC	78514
rs261692185	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77375575	CTGAGTCCCAGGAAC[A/T]CAGGGGAGCCGTTCC	78514
rs261703485	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77475868	ATACATAACAATTGG[C/T]GAAAAATTCAGATAT	78514
rs261703740	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77408717	CTTGGCAAACGCTCC[C/T]TGTCTACTTGCCCTT	78514
rs261711235	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77409419	AACGACAGTTCACAA[C/T]AAAGATGGCCCGGAA	78514
rs261720019	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77447735	TCTTCGTGAGAAGAC[A/G]CATCGTGGCCACGGC	78514
rs261720842	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77362573	TGAGAATTCCTCAGA[A/T]GACATTGGTTGGCTT	78514
rs261728929	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77318460	ACTTAAGAACAGTCA[C/T]AAATGCCTATTTAAA	78514
rs261729471	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77275089	GTGGGGGACTTTTGG[A/G]ATAGCATTGGAAATG	78514
rs261734846	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77426504	GTTAACTTACCAGAG[G/T]ATAAAAATATGAAAA	78514
rs261747585	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77270581	TGTAGCCAAGACAAT[A/G]CCCCAGCATGGAGGG	78514
rs261749874	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77356326	ATACCTTCCCCCGGC[A/C]TCCACAGACAGTGCA	78514
rs261757509	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77432545	GGTTTCGCTAGATGT[G/T]TACTGCCCATCCAGG	78514
rs261760512	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77311940	ACCTGACAGTGAAAG[A/G]GGTTTAGCTGAACAT	78514
rs261767537	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77432932	CTGTTTTACCTCATT[C/T]CGCCAATGCAACAAC	78514
rs261774737	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77474655	ACAGTACAGATGGAC[A/G]TGGAGACTGAGAAAG	78514
rs261796281	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77255590	TGTGTGTGTGTGTGT[C/G]TGTCTGTCTGTCTAC	78514
rs261801202	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77380679	CACAGAGCACAAAAA[A/C]ACAAAAAAACAAAAC	78514
rs261802222	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77297260	ATCACCCAATCACCA[A/G]ACTCAGGTGTTTTCC	78514
rs261806078	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77379459	AAGCGTCTGCACACA[C/T]CCCAGCCACTTCCTT	78514
rs261812026	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77252242	CCATGAGCACCTAAG[A/T]GGCCAGGGGGAGACT	78514
rs261815362	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77498758	AAAGCCAGCTCCCCT[C/T]ATCTCACTCCTAATG	78514
rs261817115	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77335080	CTCCAAAGGACCAGT[G/T]TCCACTTAAAGCTGT	78514
rs261821643	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77255478	CTCGCTAATACATCC[-/T]TTGCAGACTAGGATG	78514
rs261830687	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77280286	CAAACTGTCTTTCAG[C/T]GTGCTGAACCACATT	78514
rs261842614	in-del	-/CACACACACACACACACACACACACA			intron-variant	Arhgap10	GRCm38.p3	8:77273093	TTAAAGAGTAAATAT[-/CACACACACACACACACACACACACA]CACACACACACACAC	78514
rs261848710	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77504624	TCAGAGGATCCATCA[A/T]CACGGGGCGAGCATG	78514
rs261861135	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77362354	TTTGAAAAAGAAATG[A/G]TAAAACTTGATGTTA	78514
rs261869126	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77318293	ACCAATACACTCTAT[A/G]TGGCTACATAATGGA	78514
rs261874031	in-del	-/CAG			intron-variant	Arhgap10	Mm_Celera	8:77371242	CTTCAGCTACCAGAC[-/CAG]CTTACGCACATGGCG	78514
rs261881748	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77273313	TGCTGAAGACAGGTT[C/G]GGCTATGAGCAAACA	78514
rs261893274	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77356066	ACTGAAGAACGCCTA[G/T]ATTATATATAGGATC	78514
rs261897145	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77311755	GCTGCAACCACAGGC[A/G]ACCGGCACGCTCCTC	78514
rs261913922	in-del	-/GCTTTGACAC			intron-variant	Arhgap10	Mm_Celera	8:77286184	GCTCAACAGTGACAG[-/GCTTTGACAC]GCTCCACTCAGACGC	78514
rs261915369	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77310080	ATCACCCTATACTCT[A/G]CACAAAACCACATGA	78514
rs261925858	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77426211	CGTTTCACAGAACCC[C/T]ACTCCGAATTCACTG	78514
rs261935861	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77418848	AGTAGCACAATTACA[A/G]TTATGAAGTAGCAAA	78514
rs261943241	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77468950	ATAATGTTATGGCTG[A/G]GTGTCACCACTGAGA	78514
rs261944483	in-del	-/GG			intron-variant	Arhgap10	Mm_Celera	8:77381135	AAGTCGGGAAGGAAA[-/GG]GTTTATTGGCTTAGG	78514
rs261958926	in-del	-/CC			intron-variant	Arhgap10	Mm_Celera	8:77323983	GGAAAAAGACTCCCT[-/CC]CCACCCCCCCCATCC	78514
rs261985017	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77273165	AATGTAAACAAAAGG[A/G]CAAACAAGAGGCACT	78514
rs262011474	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77460149	AGAAACCCTGTCTAG[-/A]AAAATCCCAAAGGAG	78514
rs262021508	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77455534	AACTTGAAAAGAAAG[C/T]GAACAAAGAATGCAT	78514
rs262039871	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77316073	CCCTGAGGCTGGACA[A/G]CAGAGCATGCTAAGG	78514
rs262043426	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77473196	GGAGTGACCCCTGAC[A/G]CCCACTTCACAGTGG	78514
rs262048871	snp	A/G			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519534	GGGAGGGAGGGGTAG[A/G]TGGCATGGCTTTACT	78514
rs262052399	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77423415	TGGGTTCCGGGGGTT[-/G]GGGGTCTGAGGAGAG	78514
rs262068440	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77260142	TGAGTTCACAGTCTC[C/T]TTAGTGTGAGGGGCA	78514
rs262074267	in-del	-/TGAAGTT			intron-variant	Arhgap10	Mm_Celera	8:77332317	GGCCTTCTAGGACTC[-/TGAAGTT]TGGTACATGCCATGC	78514
rs262099462	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77454352	TACCAAGTGTGACAA[C/G]TTGAATGTCTTGCTG	78514
rs262109018	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77384420	CGTAGGACCATGAGC[A/G]AGAGCAACCTGCTAT	78514
rs262115342	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77497506	TAAATAAATTTAGAA[A/G]CTGGTAGGTTTAAAC	78514
rs262116881	in-del	-/A			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77502600	TTGCAAGGATGAGGC[-/A]AAAAGGCAACCAATC	78514
rs262131924	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77499453	ACCTAATCTCAATAG[-/A]AAAAAAAAGTTTATA	78514
rs262133490	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77340575	CTTTTCACCCTGGAA[C/T]GCCCTGTCTTCTTGA	78514
rs262133829	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77456135	AACAAGGGAAGTACA[C/G]ATTCAACCCAGAATC	78514
rs262135113	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77429634	AGGGAGAGAGGCCTA[C/G]AGTGGCCCCAAAACG	78514
rs262136989	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77276877	CACCCCCATCCTGTG[C/T]TTGCAGAACTAGTGC	78514
rs262148095	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77499745	TCATAACAGTAGCAA[A/C]ATTACAGTTACAAAG	78514
rs262151267	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77379228	AACAATGGTCCCCAA[C/T]ACACTTGGAACCCAC	78514
rs262154995	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77472563	ATAAATAAATAAATA[A/G]ATCTTTTTTTAAAAG	78514
rs262156065	in-del	-/CA			intron-variant	Arhgap10	Mm_Celera	8:77447417	ATCGGAGTCCAAGAC[-/CA]CATTTCAATCTCTTC	78514
rs262167515	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77334813	AGACAATTACAAGAG[A/G]AGAATAAGTTACTTT	78514
rs262169338	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77437043	GGGAGTGTGCTTTTC[A/G]TTATTAAATTTTCCT	78514
rs262180079	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77367383	TGTATAAATCCTGCA[C/T]CATATGATCCTATGC	78514
rs262185498	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77411345	ACACACACGTGCACA[C/T]GCATGCACACACACG	78514
rs262187244	in-del	-/TCTT			intron-variant	Arhgap10	Mm_Celera	8:77496621	AAAAAATGTATGTTC[-/TCTT]TCTTTCCATGCAGCT	78514
rs262203785	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77366596	GCTGGGCAGAAATAG[A/G]AATCAAATCATCTGT	78514
rs262207034	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77455129	AATACTGACCTAAAA[C/T]GACTTGAGGAAGAAG	78514
rs262216734	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77361176	AAGGGAGGGGGCTTG[C/T]GTTTCTTCCCTGACC	78514
rs262224658	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77316889	CACACACAGCAGATT[C/T]GGCTTCCAGAGCCCA	78514
rs262233472	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77360256	TCTGCAGGGAAAATG[A/G]TGCCCTGCTGGTACT	78514
rs262233657	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77260992	GTACTGGGTCACTAA[C/T]CACCTCTTTCACACA	78514
rs262251119	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77395680	AAATACAAGTTTCCT[C/G]TCAGTCAGAACACGC	78514
rs262253800	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77504085	ATCCTCAGGGAAGGG[C/T]GGGGCCTTGGGAGCC	78514
rs262255214	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77476812	ATTGCTCACCTTTTT[A/G]CTGTTATTGTTGAGA	78514
rs262260081	in-del	-/GA			intron-variant	Arhgap10	Mm_Celera	8:77441217	GCAAGACCGTCCACC[-/GA]GGCGTGAGCCTCCTT	78514
rs262264593	in-del	-/G			intron-variant	Arhgap10	GRCm38.p3	8:77283185	GAGGAGGGAGGGGGA[-/G]GGGGGAGGGAGGAGG	78514
rs262266635	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77309650	ATGATATTAACGATT[C/T]ACACATTTCTCCAGG	78514
rs262271237	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77254439	TCTTCTGGTGTTCAT[A/G]AAGACAGCTACAGTG	78514
rs262292526	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77286238	AGACCTGCAATCAGG[C/T]CCAAAGTGGTCTCAT	78514
rs262297084	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77479349	TATTACATCCTAGTC[A/G]GCTTCCATCTTGGTT	78514
rs262299551	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77338330	TATACCTGATCAATG[C/T]AAATGCTACCTAAAA	78514
rs262303123	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77333598	GGTTCCAGAGAATGA[C/T]AAATAAGAGCAGAAG	78514
rs262305350	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77457507	agaggcccattggtc[A/G]tgcagactttatatg	78514
rs262311755	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77285269	CGTGCGTGTGTGTGT[A/G]TACCAGATACAAAGA	78514
rs262312454	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77278219	CACAACTAAGATGTG[C/G]GTCCTTAGTGAGGTG	78514
rs262315321	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77265297	GGGAAATAGACAGTC[C/T]AAGTCCTGAACAGCT	78514
rs262334298	in-del	-/T			splice-acceptor-variant	Arhgap10	Mm_Celera	8:77346379	CGGGCTGCCGCTCTC[-/T]TTTTTTTTAAGAAGG	78514
rs262338040	in-del	-/CACACACACA			intron-variant	Arhgap10	Mm_Celera	8:77261002	ACTAACCACCTCTTT[-/CACACACACA]CACACACACACACAC	78514
rs262368709	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77411866	GATTAAACAGTGGGC[A/G]CACACCATCCTGCTG	78514
rs262376616	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77320327	TTACACAGAGAAGCC[C/T]TGTCTCAAAAATCCA	78514
rs262389585	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77265223	GTGGTTCTCACCACC[A/T]CACTTGCAAGGCCTC	78514
rs262391263	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77459944	TGGATGACAAGTGAC[-/AA]GTGCACGTGTTAGTT	78514
rs262411501	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77314619	AGCCTATCAGGTCTC[A/G]CTTCCTCAGGTCTTT	78514
rs262412139	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77258073	TTTCTCAATTAGTGA[C/T]CAAGGAGGGAGGGCC	78514
rs262434695	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77428219	CTCCACGTGGGAAAC[A/G]AGCCTGTCCCATGTG	78514
rs262462937	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77383455	GCAGCATCTCCAGCC[A/G]CTGCTCCAGGGCCCA	78514
rs262471204	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77283476	GAAATCTTCCTCTCT[C/T]CCACATATGCCTAGT	78514
rs262475962	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77339250	GACCTCCTGTCTCCA[C/T]GAGAATCAATGAAAT	78514
rs262478926	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77453848	GTTCACCCTGGGTAA[A/G]TAAGCCTATGCATCC	78514
rs262508229	in-del	-/CTAT			intron-variant	Arhgap10	Mm_Celera	8:77252966	GGCTTGCTTACACGC[-/CTAT]CTAAGTTCACACCAC	78514
rs262510048	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77410628	CTGAGCTCACAGGGA[A/G]TGACTTTATGAAACC	78514
rs262510980	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77253069	CTGCTGCTGCTGCTG[C/T]TGCTATAATCAATGT	78514
rs262526222	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77365867	AGGGGAAGAAAGGGA[C/T]AGATGAAGCATTCCA	78514
rs262533995	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77321147	CCTGCCTTCCCCACC[A/T]CGCTGGACCGTGTCA	78514
rs262534043	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77327723	TACTTGACTGGTGCT[-/G]GGGGAGGTGGTGCTC	78514
rs262537913	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77371277	GGCATAACTCACAAG[C/T]TGTCCTGTGACTTAC	78514
rs262543058	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77472119	TTTGCTAAAGATGAT[C/T]TTATATATACATATA	78514
rs262545171	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77434246	TCTCGATGTTTTTCA[A/T]GGTGATCCAATCCAC	78514
rs262559030	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77475594	CATGCAAACCAAACA[C/T]ACACAGGCATAAAAT	78514
rs262564623	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77315542	GACGTCCCTGAGGCT[A/C]AAGTTTTCCTTCTGT	78514
rs262565232	in-del	-/AGGAGA			intron-variant	Arhgap10	Mm_Celera	8:77475205	ACCCCAAGGAAAGAG[-/AGGAGA]AGACGCCATGGAGTA	78514
rs262566563	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77369067	CACCTTGCCAATCCA[A/G]AGAAGCACATACTAG	78514
rs262574275	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77477991	AAGCTCACGGGCCTC[A/G]CGGCCTCACAGGCCT	78514
rs262574692	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77364929	ATTAAGTCCCAGGAA[A/C]GTGGATAATCTCAGC	78514
rs262575537	in-del	-/GCT			intron-variant	Arhgap10	Mm_Celera	8:77316881	GCTTCTCCACACACA[-/GCT]GCAGATTCGGCTTCC	78514
rs262580490	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77259013	ATGTCACAGCCCTTG[C/T]GTGTGCCACCACCTC	78514
rs262586545	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77399784	ATCTACACACAAATT[A/G]ATCTACTTGAATCGT	78514
rs262600378	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77382160	GCATGAATCCTTATT[A/T]AAAAAAAAGAGAGAG	78514
rs262611142	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77452925	GCAAAATAGCAATGC[A/G]CATAAAATAAGAATA	78514
rs262622596	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77387860	CTGACTGTATAGAAC[C/T]CCTCTTCCATCTTCA	78514
rs262624344	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77435000	GGGAGCAGATTCCAG[C/T]CTGAAGCCAGCAGAG	78514
rs262626143	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77507103	ATCATGAGAAGCTGA[A/G]TTTGGATCCCACAGC	78514
rs262634761	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77284520	AGAACAAAAGAGAGA[A/T]TAAGATAGTGTTATG	78514
rs262635593	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77343263	CGTCCCAGGACCTGC[C/T]ACAGGCTTAGCATGT	78514
rs262635876	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77476405	ATTCATACATTAAGA[A/T]CATCTCTGGACACAT	78514
rs262638134	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77401926	TGACCGTCGTCGTGG[-/T]CCTCCTCCTCCTCCT	78514
rs262648333	in-del	-/GCACAC			intron-variant	Arhgap10	Mm_Celera	8:77284456	AGTGCATGCTTGAGA[-/GCACAC]TCAAGGCACCCTCCT	78514
rs262649473	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77290777	TTCCATCAAGGGGTC[A/G]AGACTCATGGGTTGA	78514
rs262653487	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77275870	TGTCCTGCAGAACCA[C/G]GATGGAAGAGCAGTG	78514
rs262655707	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77501871	CACCTGCACCAAATG[A/C]TGGTGAGGTCTTAGC	78514
rs262669414	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77265487	GGACAAGAGATGAGG[-/T]TGCCAGAATCCATGG	78514
rs262670602	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77337096	TGGTTACTCACGGAC[A/G]GACAGACGGCCTTTG	78514
rs262698584	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77313954	AGCAGAAAGCTACTC[A/G]CAACAGTTTGTTATG	78514
rs262699985	in-del	-/ACACACAC			intron-variant	Arhgap10	Mm_Celera	8:77411581	CACACGCACATGCAT[-/ACACACAC]ACACACACACACACA	78514
rs262702205	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77416274	TGTGTTTCTAGTTCA[A/G]GATACAAACCCTCAG	78514
rs262705542	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77414155	GGTCCCACGGGCAGA[G/T]AATGTCCAGGCAGCT	78514
rs262709604	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77324773	TCTAAGTTTACTACA[C/T]GTAAACCTGCATATA	78514
rs262713430	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77459895	TAATAACCACGTGAC[G/T]TTCATTTTGCATGCC	78514
rs262721701	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77363096	TGCCTGTGTCCGGAC[G/T]TCTCTGAAAAAGGAA	78514
rs262722815	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77457725	GAAAGTCTACACTCA[A/G]TAGCACCATCCAATC	78514
rs262724080	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77257718	ATACACAAGGCATGT[A/T]TACTTGTGAGCACTT	78514
rs262730987	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77500392	GTGTTATTCTAAATG[A/G]AGATATACATCCTAC	78514
rs262733510	snp	A/C			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77502700	GGTTAGGGTCTGTGG[A/C]CTGGCTCTCCTGCCA	78514
rs262741440	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77420238	GCAAGCAACGCCTGC[A/G]TCAAAACCACCATCC	78514
rs262753159	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77463040	AGGTGAGGAGTCTGC[C/T]TGAGTGAACTGTAGA	78514
rs262765140	in-del	-/GAT			intron-variant	Arhgap10	Mm_Celera	8:77332069	TCACCTACCAGAGAG[-/GAT]GATGACAGCATCCGA	78514
rs262769740	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77388769	ACACAGGTCACCTAG[G/T]GACAACGCAAACCCT	78514
rs262807858	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77440731	CGCCCCCTGCTGGCC[G/T]GTATGGGTAGCCATG	78514
rs262829601	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77413950	TATAAAAGGTGTTCG[A/C]AACGAATGACCTGAC	78514
rs262833923	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77281281	CAGCCTAACCTTGAC[C/T]GCCACCCAACTCCCA	78514
rs262840262	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77409760	TCACACTGTATTACA[C/T]CCTGTGCCATTATCA	78514
rs262840544	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77457093	TGGAATTGGGAGCAA[A/G]GCACCCATGGAAGGA	78514
rs262854896	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77364233	TCCTGGGGTCCGTGG[C/T]TTGAAACGTGCTTGT	78514
rs262855989	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77374644	TATGTTACTCTTGGT[G/T]GTGCTCTTGGTAACT	78514
rs262860172	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77500268	TGGAGATAATGCTCA[C/G]TATTGTCCCCAACTG	78514
rs262870425	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77462948	CAGCAGAGGCTTCCA[A/G]GGTGGCCCAGTGGAC	78514
rs262874036	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77434786	CCCCCAAAAGAACAG[-/C]CCCCCCAGCCCTTGT	78514
rs262916780	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77440608	CACAGACAGACATGT[A/G]GGCAAAACACCATTG	78514
rs262935579	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77481177	ATGACCGTCTACTAT[C/T]CACACTGACTGTCTA	78514
rs262941297	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77336696	CGGGAGCTGCCATTT[C/T]CACAGCCAAGTCAAT	78514
rs262951580	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77282368	AGCAGGCCAGAAACA[C/T]GGAGACAGGAAAAGA	78514
rs262957816	in-del	-/GAG			intron-variant	Arhgap10	GRCm38.p3	8:77483392	GAGGAGAAGGACTGA[-/GAG]GAGAAGGGCAGAATA	78514
rs262962255	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77369822	ATGCCCATCTTCGTG[C/T]CACCTGTTTACAGTC	78514
rs262967563	in-del	-/TAC			intron-variant	Arhgap10	Mm_Celera	8:77253049	TGGGCTATTTTTGAG[-/TAC]TGCTGCTGCTGCTGC	78514
rs262970040	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77324524	AAGATCTGAGTTGAC[A/G]GATAACCGGCATATG	78514
rs262990568	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77444503	TACAAGAAAAAGTTA[C/T]GCACCTCGAAACCCT	78514
rs262995968	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77480041	CCTTCCTAGTGAAGG[A/G]AAAGTATCCTGGTTC	78514
rs262997708	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77385776	AAACGGGAAAAGTTC[C/T]ACCTTACAGAGACAG	78514
rs263016144	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77341800	GCTAATATGGACACA[A/C]ACATCCACTCACAAA	78514
rs263016691	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77348928	CCAATGTGAGTCCAA[C/G]CCAGAAAGACGGGTC	78514
rs263018043	in-del	-/TTGT			intron-variant	Arhgap10	Mm_Celera	8:77426901	AAACCCTGTCTTGTG[-/TTGT]GGAAAGTGGTGGCAG	78514
rs263028736	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485862	GTCCTCTAGGGCAGG[A/G]GTTCTCAACCTACGG	78514
rs263037963	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77385395	ACTACTACAGCCAAG[A/G]AAGGGGTCATGGGAT	78514
rs263040381	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77255966	CTTTGCTAGAGTTAT[A/G]TGTAGCCTGGAACTG	78514
rs263079118	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77323701	AGAGTAGAGCTCCTG[C/T]CGTGCATGCCCAGAC	78514
rs263081065	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77268238	CTAAGCTGTATCCCC[A/G]CTGATAGAGATGGCT	78514
rs263094801	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77368428	ATATCCTCATAAAGA[A/G]ACAGCCTGAAGCCAT	78514
rs263095576	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77505845	GTATCTCCGAGCAGT[A/C]ATAATCTACTCATTA	78514
rs263103440	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77439257	CTGGAATCAGGATGG[A/G]AAAACAAGAGAACTG	78514
rs263108535	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77512045	TTCGAAAAAAGGCTG[G/T]AAAGAGCCAGCTGTG	78514
rs263115374	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77317637	AATGGCACTTTGAGA[A/G]GTCACGCTGGTGTGG	78514
rs263132152	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77262853	TAAATAACTGCAAAA[C/T]GCAAGTCTGGAAACA	78514
rs263139829	snp	C/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503881	CCTCACAGCAGTGCG[C/G]GGAGCTACCCACTAG	78514
rs263145319	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77323070	CAAGCATTTCACAAG[A/G]AAGAGCGGCTAGTGT	78514
rs263148571	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77263229	AAATAGTGGAGAAAA[-/G]AAAATCTCCCAGGAG	78514
rs263150409	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77417701	AGAGAGAGAATAAGA[-/T]GAATAGCCGAAAAAA	78514
rs263156485	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77431406	TTTTCCTAGGGATCA[C/T]CAACAGACAGGACAG	78514
rs263161360	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77262290	CAGTTTCTCAAGGCT[A/G]CTGTTTTCTGTCTTC	78514
rs263163659	in-del	-/CAATGGGAGCACAC			intron-variant	Arhgap10	Mm_Celera	8:77415975	ATGCCAGGAGCACAG[-/CAATGGGAGCACAC]CAATGGGAGTGTGCT	78514
rs263167720	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77287560	TTACCAAAACTAGTA[C/T]GTGCTGCTACGTGGA	78514
rs263171057	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77510015	GTAAAGCAGGGAGTC[A/G]ATATTTAATACAAGT	78514
rs263186907	in-del	-/TAGA			intron-variant	Arhgap10	Mm_Celera	8:77407404	TCCATTTACTTTAAG[-/TAGA]TAGATAGATAGATAG	78514
rs263190949	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77439143	ACCACTGGCCAGAGG[A/G]TTGCAATGAGCTCAT	78514
rs263198248	in-del	-/AAAAAAC			intron-variant	Arhgap10	Mm_Celera	8:77329927	CATTAAAAAAAAAAA[-/AAAAAAC]CATGTTTGTGAGCTG	78514
rs263199296	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77328304	CTGCGGTTTGTCCTT[C/T]CAGTTGTTTCCCTGA	78514
rs263252656	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77382019	ATTAGAGTAAGTTGC[A/G]TGTGTACATAAGCTC	78514
rs263259729	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77437249	TGTTTGAAGAATCCT[A/G]GCCCAAACAGTGCCT	78514
rs263260227	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77396314	CATAAAGATGAGCCC[C/T]ACTCCTCATCAGGAA	78514
rs263264417	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77452746	TGCATTTAAATTGCT[-/A]AAAAATGCTCCTTTG	78514
rs263267269	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77373803	TGCCTCCACCCCCAG[C/G]TTATGGTACCCACGA	78514
rs263267755	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77260704	CCTTTAACTGCTATG[A/G]TGAACACCACTGATA	78514
rs263269219	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77511802	CAAACCAAAAAAAAC[-/AA]AAAAACAAAAAAAGA	78514
rs263270132	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77478586	TCCTACCAAAGGCAC[A/G]CTTTCCATGTACTTC	78514
rs263282272	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77345934	TCATTCAAATTGTAC[A/C]GATACAGTGATTTGG	78514
rs263297680	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77412619	GTCCTCTTCCCCACA[C/T]CAGCACAGCACGAGC	78514
rs263300946	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77402575	GAAGTCTGAGGCCAA[C/G]GTGAGCAACTCAGCA	78514
rs263305486	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77293268	TTGCTTAGATGTGAA[A/G]CTGATCAGATATGTC	78514
rs263309042	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77455645	CCTCTGTAAGATAGT[A/G]CTTCAGGCGAGCTGG	78514
rs263328229	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77418292	ACATTATAAAAGGAA[A/G]GAATGTGAGGACGGC	78514
rs263334642	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77396980	GCAGACATGTGAAAG[A/G]ATGCGTGGTGTTTAG	78514
rs263337750	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77417738	AATGACGGTCCTTTC[G/T]AGGGAGAGCCTATGG	78514
rs263350813	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77460574	CTTGCAGGAGCAAAG[A/G]CACAGGTGCACCTGC	78514
rs263359247	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77504667	GCATGGTCACACAGC[A/G]AGAATGGCACACTGG	78514
rs263364993	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77294047	AACAGGAATCGTCTT[A/G]CCAAGAGAGCCCTGT	78514
rs263372295	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77339886	CTCTTAGGCAACTCT[C/T]ACACAAGCACGGGAT	78514
rs263388220	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77321077	TACATACCAGCATTC[A/G]TGGCTCTGCTCCCTG	78514
rs263406038	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77327801	GCTCTAAGATTCATC[C/T]TAGTCTTCTCTAAGT	78514
rs263407513	in-del	-/AAC			intron-variant	Arhgap10	Mm_Celera	8:77322261	GAGCCTGCAGAAATG[-/AAC]AAGATGTCTTCAAAA	78514
rs263411448	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77265717	CAGGTCTATCACAGG[A/G]ACAGAGAGGGAAGCA	78514
rs263414469	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503423	CTACCTTTCCTCACA[C/T]ATAACAAAGAAAATT	78514
rs263418339	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77366757	ATTGAGATGAATTAA[A/G]CCTTCAAGCATGCTA	78514
rs263420716	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77416140	GGGGGGGGGGGGGGG[C/G]GAGCACACTACCCAG	78514
rs263424686	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77422890	AACAAGAGGGCAGAA[C/T]GGCTTACAAGTCTCT	78514
rs263440048	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77321929	ATTCTTAAACCTTTT[A/G]AAATATGTGTGAGTT	78514
rs263449432	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77266272	GTATATTCCCAGAGG[C/T]TATGCATCATGGGCA	78514
rs263453179	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77509298	GAGCAAATCAGTGAG[C/T]GTGGAGAAGTCACAC	78514
rs263465787	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77401518	AGCCTAAAACTCTAT[A/C]CGCTGAAAAGCAGAG	78514
rs263468546	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77260277	CGAAAGGTATTTACG[C/T]GTGGGAATTCAGAAA	78514
rs263471928	in-del	-/AG			intron-variant	Arhgap10	Mm_Celera	8:77414941	CACACACACACACAC[-/AG]AGGACTATAAAGAGG	78514
rs263473995	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77464850	CACAGTGGCTCACAG[C/T]CATCTGTAATGGGAT	78514
rs263481551	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77292698	GCTAGCCACCTGCCA[C/G]GACCTCACTTTCACC	78514
rs263492124	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77436306	TGTCTCCATGGCAGA[A/G]CACCTGCTTGGCCCA	78514
rs263520315	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77338794	CTATTTCTAACCAAG[-/A]AAAAATGTAACTATC	78514
rs263523040	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77443247	ACACACGTGACTTGT[A/G]AACAGAAAGCATAGA	78514
rs263528621	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77285559	ATTAGTAAAGTCTAC[G/T]TCTGCCATTAATAAA	78514
rs263537355	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77483909	GTGACTTCCCCTTTC[C/T]CCTAGGGTGAGATGA	78514
rs263557896	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77371835	ACAAGTAACTGCACA[C/T]GGGAAAGAGGCAGTC	78514
rs263570397	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77490875	GCAAGGTCACAAGAG[C/T]CCACAGCAACACACA	78514
rs263579907	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77326669	CCTCACTAATCTGAT[A/G]ACTGTATAGCTGTAA	78514
rs263595238	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77441434	AAACCCCACCACCAG[A/T]ATAAGACCATCTTTA	78514
rs263595625	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77490107	TTGCAAACATACTGA[G/T]CTGGGAGTCAGCAGA	78514
rs263603612	in-del	-/GCT			intron-variant	Arhgap10	Mm_Celera	8:77486054	CTGTATTAAAGAGTA[-/GCT]GCATCAGGAAGGCTG	78514
rs263609086	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77400449	CTCTACCCATGGGTA[C/G]ATCTTACTCTTTTCC	78514
rs263625564	in-del	-/GAA			intron-variant	Arhgap10	Mm_Celera	8:77466070	TGCTACCAAAATTAG[-/GAA]AAAAAAAAAAAACCT	78514
rs263632099	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77352273	AACTGTATTAAGGGG[C/T]TGTAGCATTAGGAAG	78514
rs263633265	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77447583	CCCTCAACACAGAAC[C/T]TCTCTGCCGCAGCTC	78514
rs263640922	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77488880	ACACTCAAGACAATA[A/C]AGTAAGCATTCTATT	78514
rs263641036	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77298627	TCCTAGAAATCACAT[G/T]GTGGGTCACAACCAT	78514
rs263649239	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77344506	GAACTCCGTCAGAAG[A/G]CAACTGAATGTCAAC	78514
rs263652355	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77291528	TTGTGTATTTAAACA[A/G]TGTTTCTTTCAAAGG	78514
rs263675250	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77508171	GATAGAATGAGATGA[C/T]AAGTGGCTGCTAGAT	78514
rs263675972	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77370802	CTCAGAGGACCAGTC[C/G]ACTTCGTGCGGACCG	78514
rs263692144	snp	A/C			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77515686	TCATCTTTAATCATA[A/C]GCACAAGGATTAAAA	78514
rs263695855	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77270494	GGATGGCTAAACAGA[A/T]ATGGTGCTTCCTGGA	78514
rs263706543	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77353134	AGAGTGGAGAGGCAG[A/G]GGAGCTGTTTCAGTG	78514
rs263709245	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77488743	AAGCTGACATTCAGG[A/G]CCTAGATTCAAGTCT	78514
rs263714268	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77264713	CTTGTATAGGGAGAA[G/T]AAATATTCTTGCTTT	78514
rs263718347	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77415561	TGCCTGGGGGCCCCC[A/G]CTTCCTCGTGCCTTT	78514
rs263723304	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77395878	TGGAACAAAGGAACT[C/T]TCACCCATCAATACC	78514
rs263740138	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77405411	GAGATGCACACAGAA[A/G]TGTGGTGCCCACAGA	78514
rs263741833	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77345268	TAGCTCATTTTCAAG[C/T]AGCCTTTCTTTCAAC	78514
rs263748895	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77375983	GTAGCAAAACATTTT[A/T]CCAAGAGAACTCGAC	78514
rs263754303	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77496526	CCTCCTCCATGATGC[-/T]TTTTTTCCCCCCAAA	78514
rs263768351	in-del	-/TACC			intron-variant	Arhgap10	Mm_Celera	8:77460347	AAAAGAATATGAAGA[-/TACC]TTACAAATACCTTGA	78514
rs263774794	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77290020	GGGGATGAGACAGAC[A/G]TGGGAGGGGCTGGAA	78514
rs263780343	in-del	-/GGAGTCTGC			intron-variant	Arhgap10	Mm_Celera	8:77465022	ATGTTTCTGGCACAG[-/GGAGTCTGC]CGAGTGCTGAGGCCT	78514
rs263802073	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77326133	AAGCCATAGAGGTCC[C/T]GAGTTCAACTCCCAA	78514
rs263810080	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77442447	TGAGGCCCCAGGTCA[C/T]CGAGAAGTATGCGCC	78514
rs263815034	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77515551	GGGTCTTTCCAACTT[A/G]CCAAAATGGTGTACA	78514
rs263816313	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77271330	CCAAGTTCCTGCCCT[A/G]TGTGAATTCCTGTCC	78514
rs263818990	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77483427	TAAATTAAATGAAAA[A/T]TTTCAAAAGAGGTTA	78514
rs263831552	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77320570	CAAAGCTGAGAGGCA[G/T]CGGCAGGACACAATC	78514
rs263833180	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77265322	ACAGCTGTCCCATCC[A/G]AGTGTTTGAAAATGT	78514
rs263840122	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77448021	CATTCAAACACCTGA[G/T]TCTATGGGAGCCATA	78514
rs263845009	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77375467	TAGTCGAGACAGCCT[A/G]CTGCTCAAGTAAGCA	78514
rs263847175	in-del	-/CCCCAT			intron-variant	Arhgap10	Mm_Celera	8:77274425	CCTCCCAGGCATCCC[-/CCCCAT]CCCCACCCTAGCACC	78514
rs263851322	in-del	-/TT			intron-variant	Arhgap10	Mm_Celera	8:77413667	TTCCAACATCTATGA[-/TT]TTTTTGTGTGTGCAT	78514
rs263854420	in-del	-/GAAGAAGGAAGAA			intron-variant	Arhgap10	GRCm38.p3	8:77300057	GGAAGAAGGAAGAAG[-/GAAGAAGGAAGAA]GAAGAAGAAGAAGAA	78514
rs263872508	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77343719	TCAATCCTGAGCACC[C/T]GTCTTTGCTTTTCTT	78514
rs263874281	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77440915	TGCTGTTGATAACAC[A/C]AACACTAGCAAAGAG	78514
rs263874886	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77423008	AAATGAAACTGGAAG[C/T]GCCGTCTTCAGCGCC	78514
rs263877363	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77513515	AAGAAATTTCCCCAA[A/G]AGAACACCTCTGAGC	78514
rs263882760	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77290957	GTAGCCTGATAGATG[A/T]AAATCAGTCAAAAGA	78514
rs263906985	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77404709	ATTAAGAGCATGCAA[G/T]CAACTATGAAATTGC	78514
rs263909659	in-del	-/CAACA			intron-variant	Arhgap10	Mm_Celera	8:77406666	ATCTGAGAGAGACAT[-/CAACA]CAATGGCTTTCTGAG	78514
rs263911802	in-del	-/TA			intron-variant	Arhgap10	Mm_Celera	8:77354217	AGAAAATCTATTTTT[-/TA]AAAAAAAGCTATATA	78514
rs263926917	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77439835	AGACTTAGTTAATAT[A/G]AACCATAACTCAAAA	78514
rs263927576	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77356867	AAGTTGATTAAATAT[A/G]ACTTGATCTGACCCT	78514
rs263941737	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77421519	CGAATGGCTAAAATA[A/C]ACTGGAAGAAGATAA	78514
rs263943074	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77399035	CCATTTATCTTTAGT[C/T]CAAACACTCTCCAGC	78514
rs263943269	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77421018	ACAGTCAAAAGCCCC[A/G]TCGACACCACCTGCA	78514
rs263952962	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77464452	TTGTGCAAGAAGGAC[G/T]ATTTCATAAAGTCAT	78514
rs263955022	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77410173	CTACAAGAGACAGAG[-/C]CTTGCCTCAGCCTCA	78514
rs263963664	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77507605	ATAGAATTTTCCACA[G/T]GGCATCTCGGCAGCC	78514
rs263965065	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77463735	CCTATTAGAATGCCA[A/C]CAAGCAATACCAGGT	78514
rs263968710	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77264321	AAGTCCCACAAGTTT[A/C]TTGAAAGCAACATTG	78514
rs263969875	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77297105	CAGTAAGCCTAGGGG[A/G]AAGACCTGCATGCCT	78514
rs263971815	in-del	-/C			intron-variant, downstream-variant-500B	Arhgap10	Mm_Celera	8:77358355	GATTCTGTAAGCAAG[-/C]CCCCCGATTAAATGC	78514
rs263974376	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77506705	TCCGGTTTCCTCAAG[C/T]GTGACTGTTCATAGA	78514
rs263979091	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77427093	CCCAGTTTGACTACG[C/T]AATGCTCCACCCAGA	78514
rs263980530	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77252159	CCTGGGCAGCACAGA[C/T]TCACACTGCGGTTAT	78514
rs263982256	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77428940	GTTTTGGAAGAGAGG[-/T]TTTTTTTTTTTAATT	78514
rs263999730	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77469853	ACCAGGCGTATGCTC[G/T]TAAGTGCCCTTCTCT	78514
rs264008927	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77374402	GCTGCTCACAAAGCA[C/T]CTTGTCACACAAGCC	78514
rs264012897	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77399988	CTACAGATTCTGCCA[G/T]TACACAGGGTCTATA	78514
rs264015458	snp	A/C			intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77493105	CAACTCAGAGAAACC[A/C]TGACTTGAAAAACAA	78514
rs264019232	in-del	-/GGCAGGCAGGCGGGCG			intron-variant	Arhgap10	Mm_Celera	8:77416629	CAAGACAGACAGACT[-/GGCAGGCAGGCGGGCG]GGCAGGCGGGCGGGC	78514
rs264020685	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77419281	GAGAGACTGTGTCTC[A/C]GAAGATCAGGCAACT	78514
rs264024257	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77330136	CACACCAGTGCAGCA[C/T]CAACACCATAGGCTC	78514
rs264041308	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77273539	AAGATTAAGGACTGT[G/T]AAGAGAGCAGATGCC	78514
rs264047662	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77273699	AATAATCTAAACTGA[C/T]CTTATACCTGTTATA	78514
rs264056690	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77425816	TAAGAGACAGAGTGT[A/G]GGCTCACACAGTCCG	78514
rs264059184	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77324143	TGCCCATCTTTGGCC[A/C]CAGGAAGAAGTTGTA	78514
rs264061099	in-del	-/AGCAAGTTAC			intron-variant	Arhgap10	Mm_Celera	8:77513270	TGGAACTGAGTGAGA[-/AGCAAGTTAC]AGCACCCAGCATCAT	78514
rs264067849	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77268968	GCTTACCACGGCAAT[C/G]GTCTCTCTGCCAACC	78514
rs264070853	in-del	-/GGGGGC			intron-variant	Arhgap10	Mm_Celera	8:77474544	ATAAATGAACTGGGG[-/GGGGGC]GGGTCATGAAACTAC	78514
rs264080307	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77512427	AAACTGGGGCTTATG[A/G]CTTATTCCAGGTGAG	78514
rs264085360	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77462286	GAGGAAGAAAGGGTG[A/G]GTCTTCTTAAAATTC	78514
rs264106567	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77370134	GGAATAGGAAAGAGG[A/G]GTGTGAGGGACTCGG	78514
rs264116516	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77468036	CAACGAAGCAGACCC[C/T]AAGTCCCTTACAGTG	78514
rs264121033	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77404554	CCGAAAGAAATACCA[C/T]AACTCCAGAGAAGCT	78514
rs264122188	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77446901	GCACTGGGTGCTGAG[C/T]ACGTGTAATTTAACA	78514
rs264126993	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77269989	CATAAAACGGGGCAA[G/T]CAAGAAATCAAGCAA	78514
rs264127119	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77512207	CAATGGTTCATAAAG[A/G]CCCATGGACGGCAGC	78514
rs264131383	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77295502	GAGAATTACAAACCA[C/T]ACTCACTTCCACTCA	78514
rs264138417	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77487358	GCACGCACACACAGA[C/T]ACACACTAGCTGGAC	78514
rs264142824	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77251271	GAACACGCCTTTCCC[A/T]CTTCAAGTTCAAACC	78514
rs264156590	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77451721	AACTTTATTTTTTTT[A/T]AAAAATGGGCAAAAC	78514
rs264162619	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77446483	TTATTAATTCCATTG[A/C]AGTGCCCTATGGTGA	78514
rs264171908	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494312	TGTATGCCTGTACTT[C/T]CGGCTACTAGGGATG	78514
rs264176184	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77486504	ACCTAGACAGTGACA[A/G]CAACTTTTGAGCAGC	78514
rs264178776	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77268447	CAAGCAGCAAAAAAA[-/C]GCTACCCCATTTTTC	78514
rs264200120	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77380341	GACGTGCAGCAGAAG[C/T]TGGCAACAAGTGTTG	78514
rs264206336	snp	A/C			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494046	TTAAAAAGGAGGACG[A/C]AGACATAGTGCTATA	78514
rs264208266	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77374266	ATTATCTGATCCTCA[G/T]GAATCCAATTTCCAG	78514
rs264209392	in-del	-/GAGGAG			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77493303	GAGGAGGAGGAGGAA[-/GAGGAG]GAGGAGGAGGAGAAG	78514
rs264229168	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77329897	ACACAACCACACATA[A/T]CAAAAGCAATACTAC	78514
rs264246833	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77422888	TCAACAAGAGGGCAG[-/A]ATGGCTTACAAGTCT	78514
rs264255116	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77403171	TACAAGCTCTGAACC[A/G]ACAGGTGGGCAGACA	78514
rs264271407	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77355132	GCTGGGTCCCTCAGC[C/T]GCATCCCTCCCCCCT	78514
rs264275130	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77310616	AAAACATTACAATCT[G/T]AGGGGACAGAAATTA	78514
rs264300876	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77347822	AGTGATGGTATTCTT[C/T]ATGTCTAACCACGAA	78514
rs264304148	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77355523	CCAAGCTCATAACAC[A/T]TTTTTCTGACATGTT	78514
rs264308530	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77311114	AAGTAAGATTTTTCC[C/G]AAAGAAAACAAGTAC	78514
rs264319990	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77491528	AGGCCCTGCAGCTTT[A/G]GATCTGGAAGGCCTC	78514
rs264322668	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77295202	ACAGCAGTCCCTCCT[C/T]ATAACAAAGGGAGCG	78514
rs264333972	snp	C/G			synonymous-codon	Arhgap10	Mm_Celera	8:77250949	ATAATTCTGTGGAAT[C/G]AGCCCTCGCTTGCCG	78514
rs264347993	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77373007	TGATCAAGTTGGACA[C/G]CGGTCTCCCGTGTGG	78514
rs264350365	snp	A/C/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77424268	TGGGGGGGGGGGGGG[A/C/G/T]CATGGGGGGGAGGGG	78514
rs264352043	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77445192	AAAAAAGATATTCAG[-/A]AAAAAAAAGGAAGGA	78514
rs264362319	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77328489	CCTTTAACTATTTCA[C/T]TTCTGAACTCCTGTC	78514
rs264364389	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77417341	AAAGCAAATCCCTTA[A/G]GGAAAGCCCAGCCAT	78514
rs264370347	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77272659	GCTATTTCTCTTCCC[A/C]CTCTCCTCTGTCTCT	78514
rs264370700	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77467480	TACAGAGAAGAACCC[C/T]GTCTTCAAAAACCAT	78514
rs264380716	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77373206	CTTGCTATTGTCCCC[A/G]CAACACAGACTCATA	78514
rs264399046	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77353760	TCTTTGTCTCAAAGA[-/T]TTTACACAGAGCCAT	78514
rs264401777	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77407293	TACAACTCCAGTTTC[A/T]GAGGATCCAATGCCC	78514
rs264405478	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77473020	ACACAGCCCTAGTGT[C/T]CACACTGACAGCATT	78514
rs264413953	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77266897	ATGGGACTTGAAAGC[C/G]AGCGTCTTCTTACCT	78514
rs264422958	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77445130	GATAGGGAGTTGGTA[A/G]CCAACTTCCAGACAG	78514
rs264425932	snp	A/T			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519325	CTGAGGCAAGAGGAT[A/T]GAGAGTTTAAGGCCA	78514
rs264435154	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77444825	CCTCTCAAGACGGAC[A/G]CAGCATTTCAGCTCA	78514
rs264435625	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77402513	CATTTCTCAGCAGGA[C/T]TTAATAGTATGCACC	78514
rs264444810	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77293424	CTTCCTGATAGAAAC[A/G]GGCTTTATACAGACA	78514
rs264446472	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77446088	CATTGTTTTTTTTTT[-/C]CTTCCACAGATTTTA	78514
rs264452529	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77267399	CATCTTAGGGTTACA[C/G]CTTTGGTCCAATCTT	78514
rs264486812	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77326379	ACAACCATCTGTAAT[A/G]TGATCCGATGCCCTC	78514
rs264494890	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77271420	CCCATTTGCTTCTTG[A/G]TCCTGATGTTTGGCT	78514
rs264503161	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77421665	AGCTTCTACCTAAAA[A/G]CCATGACGTTTTGTG	78514
rs264525486	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77334152	GGAATACAGGCCAGC[C/T]CTTAGTACTCACCTG	78514
rs264528725	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77448441	GAGATTCCAAGTATG[C/T]TATGTGTACATGTTC	78514
rs264539130	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77457200	TAATCAGCCTCCAAA[C/T]GCTGACACCATTGCA	78514
rs264540786	in-del	-/CT			intron-variant	Arhgap10	Mm_Celera	8:77345862	ATGTGTCCACTGGCA[-/CT]CTTTCAAAAGGCACT	78514
rs264541297	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77428011	GGTATAATAAAAACT[A/G]GCAGCAAAGTCCTAG	78514
rs264543419	in-del	-/TCTCTCTCTCTT			upstream-variant-2KB	Arhgap10	Mm_Celera	8:77519918	CTTATATGTGCTCTC[-/TCTCTCTCTCTT]TCTCTCTCTCTCTCT	78514
rs264553359	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77406950	AACACGTACATGGGG[G/T]CTGGAAACAACAATA	78514
rs264557639	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77327770	GTAACACACGCAGGC[A/G]CTTCCAGTTATGAAT	78514
rs264557934	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77470869	GATGTCTGATCCTCG[A/G]GAACTGGAGTTACAC	78514
rs264558898	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77406305	CCAGATAAAGACTGA[A/C]ATTTACAGAAGGAAA	78514
rs264563785	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77515069	AAGAATTAAAAAAAA[A/G]AAAGCTTCAAGACAT	78514
rs264564340	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77440205	CAAACTCAAAAGGGG[-/AA]AAAAAAATCAAAGAA	78514
rs264566086	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77272183	CAGCGTTTCTGTATA[A/G]CGCTGCAGAGATAGG	78514
rs264570265	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77360334	ACCACCCCAGCTGTG[A/G]CCCGCTGTCTGAAGA	78514
rs264572690	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77423879	GCACAAAGAGTCCTG[A/G]GCAGGTGTGCAGTGC	78514
rs264585956	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77467055	GCGGGACTCAGCAGG[A/G]CTAAAGGCAGAATGT	78514
rs264595155	in-del	-/AGAAA			intron-variant	Arhgap10	Mm_Celera	8:77464088	AAGGAATCTATTCTT[-/AGAAA]AGAAAAGACTGTTAG	78514
rs264598072	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77353896	GTCAAAATAAGTTTT[C/T]GAAGTAGCCACGGAA	78514
rs264603303	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77510273	CAGGCCCAAGGAATA[A/G]TTTTTAAATGCACAT	78514
rs264603959	in-del	-/TTTTTT			intron-variant	Arhgap10	Mm_Celera	8:77508131	GTCTTTCTAGCTGGG[-/TTTTTT]TTTTTTTTTTTTTTT	78514
rs264605959	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77448104	AAAGATCAATGACAA[C/T]TGGCCACATGCTTGG	78514
rs264615095	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77308491	AACAGAAGAAACACT[A/G]GCCAATTCATTCTAT	78514
rs264616931	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77472657	TATAACTATATTAAT[A/G]GATTATATGTTATTT	78514
rs264623065	snp	A/G			upstream-variant-2KB, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77518249	GACGCCTGACCGAAC[A/G]GGATGGTGGGTTTGT	78514
rs264628806	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77254019	CAATACATCGGACCA[A/C]ATGGGGACTTTGGCC	78514
rs264629382	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77382219	GGGACATGTATGCAC[A/T]CAGGAGGGACATATA	78514
rs264635599	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77453874	CATCCTTTTCCTCCA[C/T]GAACAAACAGTTTGG	78514
rs264642875	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77497208	TGTATCTGGAAGCCA[A/G]AAGAAAGAAGTGGGC	78514
rs264646766	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77376200	AAACAAAGGAGGAAG[A/G]AAAGCTGAAGAGTTC	78514
rs264652207	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77252660	CTTTCCCATCTCAGG[G/T]CAGGGCCAGCGTTGT	78514
rs264667720	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77450143	AGTCTGTGTAACTGG[-/A]AAAAGACACACAAAC	78514
rs264668315	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77405125	ACTACATCTGTTAGC[A/G]AGGTACCAAGTCACA	78514
rs264672683	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77452719	CCGTCAGTCCAGTCA[A/T]ATTTGTGTGAATGCA	78514
rs264677692	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77357949	TGTGGTAGTTTGAAT[A/G]ACAGCCCCACGGGCT	78514
rs264680314	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77496022	GAAACAGATAGTTGT[G/T]TGGTTATTTTAAGAA	78514
rs264683069	in-del	-/ACAT			intron-variant	Arhgap10	Mm_Celera	8:77385261	CACACACACACACAC[-/ACAT]ACACATACACTCACT	78514
rs264693780	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77351925	GATGCACATCAGGTT[G/T]CATATCTAATCTTGG	78514
rs264703066	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77298250	ACTCTAACTATTCTG[A/G]TTTGATTCATTTTAT	78514
rs264714682	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77375146	TGCACAACTCGGGTG[C/T]AAGCGATGGAAAATT	78514
rs264720281	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77476517	GAAAATTAAAGAATT[A/C]ATGCAATTTGATAAA	78514
rs264721934	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77330992	CTCGAACATTCTCGG[A/G]GCCGGGGTGGGGGCT	78514
rs264757412	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77409823	CGTAAGGATTGACCT[G/T]AAACCTCACTATACT	78514
rs264762140	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77447325	CATTCGCCTCAGTCA[A/G]AAGCACTGTTAGCTG	78514
rs264771858	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77251977	GATGGTTCCTTCTGA[C/G]TGTTCTTCTTACTGA	78514
rs264811887	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77336720	AGTCAATGATATGGA[C/T]GTGAGGCAGGCGGTG	78514
rs264814265	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77451433	GTAACTTATAATCTT[A/G]AAGACTATGATTGAG	78514
rs264823845	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77396849	AAATGAATCAGAAAC[-/A]AGGGAATGAGCTGTC	78514
rs264826167	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77408877	AAGCAGCAACAATTA[C/T]ATTTGACCTGAAAAA	78514
rs264832549	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77362781	AATGAAAGGAGAACC[G/T]TAAGAGAACTCTAAC	78514
rs264844822	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77469710	CATCGGCACCAGTCA[G/T]GCATGTGGCATACAG	78514
rs264845732	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77426193	GGACCTCCATCGCTG[C/G]CCCGTTTCACAGAAC	78514
rs264851449	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77356588	CCAACCCTCCTCCAA[A/C]CCACAGTCACGACTC	78514
rs264852457	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77433406	TGTGTGCATGTCCCT[C/T]CTCTTGGCCTCACAC	78514
rs264860541	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77312363	CTACACTTGAATTCT[A/G]CCAACAAGGCAGATG	78514
rs264861298	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77475204	AGACCCCAAGGAAAG[A/G]GAGACGCCATGGAGT	78514
rs264870519	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77425007	AAGAAGTGCATGCTG[A/T]TCTTATGTAAGTCGT	78514
rs264871568	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77379857	TTTCTGCTCTGTCTA[C/G]CATGACTGGTTTACA	78514
rs264879019	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77335494	GGTACCCAAGAGCAA[C/T]GTCACACTAACAAGC	78514
rs264883995	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77280837	GTTTGCAAGTAGGTA[C/T]GTTATCAAGTTCTCA	78514
rs264887060	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77431225	TGGTAAGGCAAGGAG[A/G]AGGGTAATATCTATG	78514
rs264895602	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77474004	CACTAACAAGCAGCT[A/T]GATGGACAGCCCCGC	78514
rs264905707	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77273463	ATATTCTCATTAATA[C/G]AAGTATGCTAAAAAT	78514
rs264916470	in-del	-/TGTGTGTG			intron-variant	Arhgap10	Mm_Celera	8:77326477	GTGTGTGTGTGCACA[-/TGTGTGTG]TGTGTGTGTGTGTGT	78514
rs264922450	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77310328	GTGCAGACACCCAAA[A/G]CCCCACAGTCACAGT	78514
rs264924881	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494002	CTCAATAAGTGATGG[C/T]TACACTGTTTAGGTA	78514
rs264930571	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77421748	GCTGAGCAGTTAAAC[G/T]GTGGAGTTGAAAGCA	78514
rs264956329	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77301066	TCTGGCGCTCTGGCG[C/T]TCTGGTGCTCTGGCT	78514
rs264960342	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77385125	GTCATCCAATGACCG[C/T]CTGGGGTAGAAGTTT	78514
rs264998904	in-del	-/TGTGTGTG			intron-variant	Arhgap10	Mm_Celera	8:77255573	CTGTGCACGAGTCTC[-/TGTGTGTG]TGTGTGTGTGTGTCT	78514
rs264999909	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77408044	AGCCTAGCCTACCTC[C/T]TGAGGCTAGGTTCAG	78514
rs265003804	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77454644	ATACACACTCAGTAC[A/T]GATCTGTTCACAGGT	78514
rs265009143	in-del	-/CA			intron-variant	Arhgap10	Mm_Celera	8:77455260	TGCTCAGCATGCTTT[-/CA]CACATAACGCAGAAG	78514
rs265011113	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77498030	AGTGGTGTCACTCCA[C/T]AGACTGGGAAACCAA	78514
rs265012185	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77498976	CCTCTCTCTGCCTCG[-/C]CCCCCTGCTCCCTGC	78514
rs265020171	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77262037	GCATGGCTGTGAGAA[C/T]GGGCCCTGTAAAGAT	78514
rs265020186	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77460313	TCAGCCTCCAGACCC[A/G]TTTATTACAATGTCA	78514
rs265020982	in-del	-/CTCT			intron-variant	Arhgap10	Mm_Celera	8:77511848	CTGACTGGCCTGGAA[-/CTCT]CTCTCTCTCTCTCTC	78514
rs265022438	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77355007	CCTCTCTCACAGCCT[A/G]GGTCAGCAGGAGACC	78514
rs265041066	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77437387	GCTGGGCGGCATAAA[A/G]GCACATGTTTGCAAT	78514
rs265045861	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77378521	TCACTACACAGTCCA[G/T]GTGTGCTGTGCTACT	78514
rs265050502	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77478713	ACTATCTGTGTGCCT[C/G]TTATCAGAACAGTCA	78514
rs265053641	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77334005	AAAGAAAGAGATTAT[G/T]CAAGAGCTGGGGAAG	78514
rs265055989	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77411501	ATGCACGCACACACG[C/T]ACACACATACACATG	78514
rs265086583	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77396002	TAAGATCTGTGTCCA[C/T]CTATACAAGATTTAT	78514
rs265087014	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77477284	CACTAAGGGAAACTT[C/T]TGACTTGATCTAAGA	78514
rs265102055	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77382839	TAGTCACTGGATTTC[C/T]TTCCCTTACAAAAAG	78514
rs265102942	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77499452	AACCTAATCTCAATA[-/G]GAAAAAAAAGTTTAT	78514
rs265103759	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77483493	AATGAAACATTTAAA[C/T]ACCTAAGAAGCTGAG	78514
rs265106089	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77254002	TACACATGGAAACCA[A/G]CCAATACATCGGACC	78514
rs265108900	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77338557	GCATCCTCCCCATTG[C/G]CTAACTCCTAGCATC	78514
rs265114364	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77285583	TAATAAAGGAAATGG[A/G]GAGGGAGTAACCGAA	78514
rs265133604	snp	C/G			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503632	CGAGGGGGCTCTACC[C/G]GAGGCAGACTCCACC	78514
rs265134591	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77365315	GTTCATTGTCAAAGT[A/G]CTATATTAGCTTCGT	78514
rs265142859	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77321727	GCTGCCTATGGAGAT[G/T]TCCAATTACCCTGAT	78514
rs265147952	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77358936	TCCACTGGCACTACC[A/T]CTATGTCCTGAGTAG	78514
rs265155210	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77315083	CTACTGAATTTCACC[A/G]TGCGCTAGTTAAGTC	78514
rs265169029	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77258354	TCACTAAGACAGAAG[C/T]CATACTCGGCTAGAT	78514
rs265183865	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77435935	ATGATAGGAAACATG[A/G]CAGCATCCAGGCATA	78514
rs265186978	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77507676	GATGTGAACTTCTCT[A/G]CTGCCTTCCTCTATG	78514
rs265190539	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77283857	GTCAGCCAAGGTGTA[A/G]CACAGGCTGTAGCAA	78514
rs265215658	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77370066	CACTAAACTGGTGAG[C/T]GATGATGAACAGGAG	78514
rs265221505	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77434412	TAAGCACACACATCT[A/C]TGTGCCCCTCCAACA	78514
rs265230674	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77475856	GACAATAAGCTCATA[C/T]ATAACAATTGGTGAA	78514
rs265232765	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77410219	TCTATGTACATCCAT[C/T]GCTACTAAGGCCCCT	78514
rs265235421	in-del	-/GGCGGGCG			intron-variant	Arhgap10	Mm_Celera	8:77416634	ACAGACAGACTGGCA[-/GGCGGGCG]GGCAGGCGGACGGAC	78514
rs265237018	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77441069	GGAAGGGGGAGCCAG[C/G]CCAGAAAGGCTTCCC	78514
rs265240771	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77470956	CAGCCAGTGCTTTTG[-/T]TTTTTTTTTAAGATT	78514
rs265250760	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77453124	TTAAATAAATTCTTC[A/T]CGTTAATTGAAAAGC	78514
rs265256497	in-del	-/C			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77485118	TCTGTAAGGAACTAA[-/C]AGCCATCTCCCCTGA	78514
rs265261453	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77415593	CACCAGAATAAGCAG[G/T]GTTATTTGTAAAATA	78514
rs265269454	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77343855	CCGCATTCCCAACAC[A/G]CACCATCATGGGGCA	78514
rs265278858	snp	C/T			intron-variant, missense	Arhgap10	Mm_Celera	8:77502026	ACCTACCTTCATGTA[C/T]GCTGCTCCACATCGA	78514
rs265280085	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77381718	TCCCTCAGTAAGAAT[G/T]TATGTGCATATGTAT	78514
rs265287197	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77300361	acctcacaccagtca[A/G]aatggctaggatcaa	78514
rs265295660	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77370193	AAAAGCTTTGATTCC[C/T]AGTGTTGGGGGTTGG	78514
rs265304607	in-del	-/ACACACACACACACCA			intron-variant	Arhgap10	Mm_Celera	8:77273124	CACACACACACACAC[-/ACACACACACACACCA]AATAAATGTAAATGT	78514
rs265304626	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77409369	TCCAGTCTTCAGCCA[A/G]GATAGAGCTATGACC	78514
rs265312307	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77314278	AGATAAGCAAAGCTC[-/T]TTTACTTTAAATTGC	78514
rs265313209	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77363528	CAGCAAGCCTGTCTT[C/T]CCCACAACTGAGTAC	78514
rs265317115	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77500775	CCCTTACTCACGGAG[C/T]CCTCGCTCTAGCTCC	78514
rs265317198	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77319547	GTCTAAGCATTCACC[C/G]CCTGTGACAACTTTA	78514
rs265321731	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77463358	CCACTTTATAAAGCT[C/G]TGTAACAAGGTTTAC	78514
rs265328105	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77337448	CCCCTGCGCTAACCT[-/C]CCCCTATTAGAAAGG	78514
rs265332035	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77264411	CACTTCCTGCAGCTT[C/T]TCCTATGGAGGAAGA	78514
rs265334110	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77506384	GTACAGGCTTCGGCA[A/G]TGGTGCCACCTCCAT	78514
rs265334779	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77313298	CAAATTCAGAGGACA[C/T]GGATCTGCTTAAGCA	78514
rs265335703	in-del	-/TGTTGTTGTTGT			intron-variant	Arhgap10	Mm_Celera	8:77347382	CTTTGTTTCATTTTC[-/TGTTGTTGTTGT]TGTTGTTGTTGTTGT	78514
rs265342673	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77257009	ATTTAAGAGCTTGGT[A/G]AGGGATGATGGAAGT	78514
rs265349102	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77289469	CATACACTCAGAGGA[C/T]AAAGCAGAAGGCGTT	78514
rs265357807	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77481863	GTTGGACGCTCTGAG[C/T]AAGTCATAACTAGTT	78514
rs265359101	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77336102	GTTAGTTAGAGAACT[A/G]GTAAAGCCTATGAAA	78514
rs265373241	snp	A/C/G			intron-variant	Arhgap10	GRCm38.p3	8:77281530	TGATGCATCCCTTCC[A/C/G]GACCACAAATATCTC	78514
rs265395168	in-del	-/CTCTCT			intron-variant	Arhgap10	GRCm38.p3	8:77309598	ATACAGAGTGGGCCC[-/CTCTCT]CTCTCTCTCTCTCTC	78514
rs265407866	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77486294	CTTCAGTCCTGCTTC[A/G]GCCTCCATGGAGTTA	78514
rs265420484	in-del	-/AGAG			intron-variant	Arhgap10	Mm_Celera	8:77343125	GCTCAATGGTCCAGC[-/AGAG]AGAAACAGTCAACAC	78514
rs265442959	in-del	-/TGACCAGGGTA			intron-variant	Arhgap10	Mm_Celera	8:77505381	GAGAACTAAGAGTTC[-/TGACCAGGGTA]TGACCCATAGGAGCC	78514
rs265445365	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77413045	GTCTAGGTGTGTCTA[C/T]GTGAGTGAAGATGCT	78514
rs265445932	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77385992	ACAGGGAAGAAATCC[A/G]CTGTGCCTCACAGTC	78514
rs265451736	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77342030	AGCCTCAAGCCTTGC[A/T]TACAGAGCCAGCCCA	78514
rs265469477	in-del	-/CCCCCT			intron-variant	Arhgap10	Mm_Celera	8:77405988	TGCTGGCACAATACC[-/CCCCCT]CCCCACAGTGCACTG	78514
rs265471751	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77336020	cacacacacacacac[A/C]TACCTACATGACACT	78514
rs265475698	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77432430	AAGGCTGGCATAGTG[C/T]CACAGTTCCCTATAA	78514
rs265476140	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77368926	TTTTTAAACAAGCCA[C/T]ACTGTTAAGTCACAA	78514
rs265491415	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77362267	AAGAGATGCAAGATA[G/T]GAAACGGAATTCAAG	78514
rs265493515	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77439667	TGCATGTGTACTTGC[A/G]TGCACACATCCCATA	78514
rs265494047	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77268649	TGTTATGGCCCCCAA[A/G]GTCTCTGTGTAGACA	78514
rs265498466	snp	A/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77480520	CGAACTCAGAAATCC[A/G/T]CCTGCCTCTGCCTCC	78514
rs265504466	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77262983	GAGTGAAGTAAGGCA[G/T]TAAACAGGCAAATAA	78514
rs265515291	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77421218	CAAGATCGTGGCTTT[-/AA]AAAAAAAAAAAAGGA	78514
rs265516899	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77384405	AAGGCCTACGGCATG[C/T]GTAGGACCATGAGCA	78514
rs265517985	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77467250	ACTCCTCTTCTACAG[A/G]AAAAGCAAACATACG	78514
rs265521311	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77340538	GCCATATAGATTAGA[C/T]AGGAGGTTCTGCTGG	78514
rs265523908	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77510366	TTCTACTCAGAAAGA[G/T]CTGGGAAGTTCAACA	78514
rs265524744	in-del	-/AC			intron-variant	Arhgap10	Mm_Celera	8:77411405	CACGCACACATGTGT[-/AC]ACACACACACATGCA	78514
rs265529715	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77438050	CGGCTAAACCAATTC[A/G]TTATTAAATAATTTA	78514
rs265533835	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77287730	GTGGATTTCTGAGTT[C/T]AAGACCAGCCTGGTC	78514
rs265535224	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77479221	AGTCTTCTGTGCCAA[C/G]TAAGTGTCTCTCAGG	78514
rs265568064	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77418648	TGTTCTCATTTTACA[C/T]GAGTCCCATAATACA	78514
rs265574130	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77461914	AAACTTTGATTTTTG[A/G]CCTGTCTTTTATTTA	78514
rs265575077	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77480549	CCGAGTGCTGGGATT[-/A]AAAGGCGTGCGCCAC	78514
rs265580096	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77260864	GGTAGCACAGCACGC[A/G]GTAGGCTAGTCCCTC	78514
rs265580102	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77505269	ATTCCCTAAAGTAAT[A/G]ACTACAGACACTATA	78514
rs265595540	in-del	-/CTGCG			intron-variant	Arhgap10	Mm_Celera	8:77322034	GGAGACCACCACCTT[-/CTGCG]CTGCAGTCTCTTGAG	78514
rs265604771	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77397832	GTGAAGGGCTGCCTC[G/T]GGAACCGAAACGTTC	78514
rs265610755	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77347535	TGCTGGGATTAAAGG[C/T]GTGTGCCACCACTAC	78514
rs265644465	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77411850	CTCCTCAGGCACTAC[A/G]GATTAAACAGTGGGC	78514
rs265644998	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77460095	TTCCAGTGCAGCCTG[C/G]TCTACAAAATGAGTT	78514
rs265647209	in-del	-/GGGGGGGGGGGGGGGGT			intron-variant	Arhgap10	GRCm38.p3	8:77413916	AGCCATCTACGGGGG[-/GGGGGGGGGGGGGGGGT]GTTATAAAAGGTGTT	78514
rs265650867	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77367216	AAACCCTTAGAAGAA[A/T]GGGTTTCTGGAACAG	78514
rs265653574	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77422236	CCTGAATCTCTTACA[G/T]AAACACTGTCACATG	78514
rs265659471	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77465022	ATGTTTCTGGCACAG[C/G]GAGTCTGCCGAGTGC	78514
rs265661181	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77402019	ACCCACTCTTACCCC[A/T]AGCCCTCATTCCCAA	78514
rs265662820	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77266851	GAAAACATTGGTTTA[C/T]CACAGGGATTCCCAC	78514
rs265663876	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77319606	ATTAATAGGGGACAT[A/G]AATGCTCTTCTCTCC	78514
rs265665253	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77508723	TGAATACTAAACACT[A/G]TCACCCCGCAGGTTC	78514
rs265684649	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77443352	GTCACGGGGAAGCCC[A/G]CAGTTAAAGAGTATA	78514
rs265688661	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77484151	AAATCGAATCCACTG[C/T]GCTCCTCAAGGACTT	78514
rs265702696	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77285959	ATTTCTGTACTCAAG[C/T]AATATGCTGACTTAA	78514
rs265705162	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77491197	CCACATGATGGCTCA[C/T]AACCACTGGTAATGG	78514
rs265706685	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77372130	CTCTTTCAGGGTGGA[C/T]AGCCCCAGGGCTCAC	78514
rs265725412	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77482608	ACGTCACATAAAAAA[A/G]GTAAGTGGGAAAACC	78514
rs265729014	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77400741	TGGCTCCTTCAGATC[A/C]CACGCCTAGGCCATG	78514
rs265736341	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77447782	AGCATTAAGCTGGGG[A/C]TAGCTTATCATTCAG	78514
rs265740285	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77489295	GTGTGTGTGCGCGCG[C/T]GCACATGAGCGTGCA	78514
rs265745127	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77388942	ACCTCCAGAATATTG[C/T]GGGAGGGGTGTCTTA	78514
rs265750976	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77344893	CTTAACAATAACGTA[A/C]GAAAAAACAGAAGAA	78514
rs265763509	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77292002	AAATCTTGGTTTTTT[A/T]AAAAGAAGATAATAA	78514
rs265786356	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77270649	CAGCACCTTTAGCAG[C/T]TGGGAAAAGGAGACT	78514
rs265786932	in-del	-/ATC			intron-variant	Arhgap10	Mm_Celera	8:77399255	TGAAGCAGCAAAGAA[-/ATC]ATCTTATGGTTGGGA	78514
rs265792073	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	Mm_Celera	8:77516186	CTGGTCATTTCTCCA[C/T]ATTTACTGACTCTCC	78514
rs265808772	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77265008	CAGAAAACGCCACAG[A/G]ATTTCTTCAGCAGAG	78514
rs265816424	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77363063	TTTCCCTGCCAACAA[-/C]AGAATGACGTCCTAA	78514
rs265823980	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77441866	AGGATTTACTCCCAA[C/G]TTAGCACCCACTTTA	78514
rs265826254	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77290325	ACCACTTGTAAAGAT[C/T]AATGGAAGACTGCAG	78514
rs265837471	in-del	-/GG			intron-variant	Arhgap10	GRCm38.p3	8:77465854	ATATAAAGTTGGAGT[-/GG]GGGGGGGGGGTCAGT	78514
rs265858631	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77440408	CTCAAATCCCCACTG[C/T]ACCCTCAGGAGCTAG	78514
rs265863880	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77375593	GGGGAGCCGTTCCCC[C/T]TTGTAAGCTGTCATG	78514
rs265875502	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77447032	TTTGAGGGGTAGGTT[G/T]TTTGTTTTGGTTTGG	78514
rs265882545	snp	C/G			intron-variant	Arhgap10	Mm_Celera	8:77415042	GGCATTATTCATTGC[C/G]GTAAGATTCCTCCCA	78514
rs265887257	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77404874	TTGAACTCAGAAATC[C/T]GCCTGCCTCTGCCTC	78514
rs265898992	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77421181	GCAGGAGGACATGTC[C/T]AGGGCTAGACTGGAC	78514
rs265904633	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77399414	CCTGGAAACATTAAA[A/G]TTGAGGAGTTCCCAT	78514
rs265904859	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77464248	CTCCAGCTGTGACAC[A/T]GAGGTGTCATGGGGA	78514
rs265921298	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77470458	AACTATCGACAGCTC[C/T]GATTGCTCCATTGTT	78514
rs265922079	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77297354	TGGCTACTCTTCCAA[A/G]GGATCCAGGTTCAAT	78514
rs265927267	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77514067	CTCCCAACCCAACCA[C/T]CCATCCCCCACGCTG	78514
rs265927832	in-del	-/ATACATC			intron-variant	Arhgap10	Mm_Celera	8:77315207	ATTCTCCCTCCCAAA[-/ATACATC]ATTGTGGGGCTGTGG	78514
rs265930255	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77342919	TGTAAATTTATGTGT[A/G]GCCAAACTGCTCCAA	78514
rs265935104	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77419521	CCAATTGGCTTTGCA[G/T]GGGTCCTGGGATTCG	78514
rs265935808	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77374610	TATCACAGCCCACGC[C/T]TACCCTGAGGGGCAG	78514
rs265943202	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77330296	CAGAAGGGTTTTCTT[C/T]ATGGAAGTGGGAGGA	78514
rs265944515	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77462896	TCTGAGAAGGTAGCC[A/G]AGGGTCTAAAAATCA	78514
rs265944984	in-del	-/TG			intron-variant	Arhgap10	Mm_Celera	8:77470954	AGCAGCCAGTGCTTT[-/TG]TTTTTTTTTTAAGAT	78514
rs265952476	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77369791	AGTCTGCTCTGCCAC[A/G]TGCTATCACACAGGG	78514
rs265969963	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77512789	GACTGGTTCCACTCA[C/T]TGTCAGAAATGGCAA	78514
rs265970333	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77487116	CAAAAAAAAAAAAAA[-/T]TCAATTTTTTTTAAA	78514
rs265970435	snp	A/C			intron-variant	Arhgap10	Mm_Celera	8:77269272	CCCAGAGGCCACTTA[A/C]TGTAATCCTCCCTGG	78514
rs265977135	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77421924	CACTGTATGATTCCC[C/T]CTCCAGATTCCCGAG	78514
rs265985588	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77295918	TCCAAGCAGAAGGTG[A/G]TGCTGCTTCAAGGTG	78514
rs265988850	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77487649	ACACAAAACAACCAT[A/G]AGAGACAAGGCAAAG	78514
rs265991574	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77251420	ACCTAGAATGCCCTT[C/G]CACTTCTTCACTGGG	78514
rs266005438	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77512687	CTAATGGGATTTAAC[-/A]AAATATTCAGATGTG	78514
rs266005640	snp	A/C			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77494622	CTACAAACAGATGAA[A/C]CAGGTCCCTCCGCAG	78514
rs266010109	in-del	-/TTTTT			intron-variant	Arhgap10	Mm_Celera	8:77412386	ACTTTCCACCTTACC[-/TTTTT]TTTTTTTTTTTGGAG	78514
rs266016390	in-del	-/GGT			intron-variant	Arhgap10	GRCm38.p3	8:77424287	GGGGGGGAGGGGGGG[-/GGT]CATGCACTGCAGGGC	78514
rs266053055	in-del	-/GAACG			intron-variant	Arhgap10	Mm_Celera	8:77324045	TCTCCCTTCCAAAGA[-/GAACG]GAACGGCCTCCCTTG	78514
rs266063932	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77403642	TATATTCAATTCATC[C/T]CGCAGTCCATTTGAA	78514
rs266064434	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77421013	TGGAACAGTCAAAAG[-/C]CCCCGTCGACACCAC	78514
rs266067740	snp	G/T			intron-variant	Arhgap10	Mm_Celera	8:77450062	GCAAGCTCTAATTAT[G/T]TTAAAGCAGTGGGGG	78514
rs266073162	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77355829	CCTGAGAGGTGAGAG[C/T]GGAAGCACAACTTAC	78514
rs266076036	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77491678	GGCCAGAGCTCCCGT[A/G]GCCACATTACCAGGG	78514
rs266078403	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77418205	ATATCTCCCCTCTGC[A/G]GGTTTTGCTCACCAG	78514
rs266080721	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77398250	TCATTCCGAATGGCT[A/G]TGAGCCACCATGTGG	78514
rs266089999	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77348811	CAGAAGGCACAGGCA[C/T]AACCCAGAAATACAA	78514
rs266121523	snp	A/G			upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77519620	CTCTGCCTCATTCTT[A/G]TGAATTAAGATGTAA	78514
rs266125949	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77445725	AGAGTGTGGAAGAGA[A/G]GAGAGCAGCCATGCC	78514
rs266132019	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77273004	ATAGCATAAGAGATA[A/T]GTGGTGATATCCAGA	78514
rs266133348	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77485826	TGGGAAAAGCAGGTG[C/T]CAAGCACTATGAAGT	78514
rs266147763	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77309163	TCTGACATTTGCTTG[C/T]TTCACTGTTTATTAA	78514
rs266165537	snp	A/C			intron-variant, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77517369	CGCCAAAGCGTGCTC[A/C]GCTGGGCCAGGCGGG	78514
rs266172147	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77294016	ACAACCACTTAGTGT[C/T]CTTCTCATTCTCCTG	78514
rs266178268	snp	C/T			downstream-variant-500B	Arhgap10	Mm_Celera	8:77250108	CCCAAAGAAGCCAGT[C/T]AGGAGGGCTGGTCAT	78514
rs266203867	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77359635	GGGTGTGGGGACCCC[A/G]GGTGTATGTAAGAAC	78514
rs266211629	in-del	-/GGAGCACGGCAATA			intron-variant	Arhgap10	Mm_Celera	8:77415980	AGGAGCACAGCAATG[-/GGAGCACGGCAATA]GGAGTGTGCTTCCCA	78514
rs266224018	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77306909	TATATCCCAGAAAAA[A/G]CAAGAAAGAAATTTT	78514
rs266240343	snp	C/T			intron-variant	Arhgap10	Mm_Celera	8:77423201	GGTCACTGAAGGGAG[C/T]CATGCAACACTACCT	78514
rs266250053	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77466215	TGTGTGTATGTGTGT[A/G]TGTGCACATGCACAA	78514
rs386835809	in-del	-/TCACCAGCCAATAGCTGG			intron-variant	Arhgap10	Mm_Celera	8:77445476	TGGTAAATAAAGATG[-/TCACCAGCCAATAGCTGG]GGAGGAGAGACAGAG	78514
rs386836787	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77425460	CAGGAGAAGGAAGAG[A/G]AGGAGGAGGAGCAGG	78514
rs386837186	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77438532	TATTTTTCTTAAGGA[A/G]CTGAGCTGGTAAAAG	78514
rs386837649	in-del	-/TA			intron-variant	Arhgap10	Mm_Celera	8:77326921	ATTTAAAATATGATA[-/TA]ATGTTAGCTAAATAC	78514
rs386837725	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77496781	AAGCAAGGTCTCTCT[C/T]TATTTTACACAGCTC	78514
rs386843295	in-del	-/GTTT			intron-variant	Arhgap10	GRCm38.p3	8:77373536	CCAGGCCAACTGTCT[-/GTTT]TCCTGTCAAGTGTCT	78514
rs386845632	in-del	-/G			intron-variant	Arhgap10	GRCm38.p3	8:77449446	TTCTTACATGGGTTG[-/G]GGGAAGCCAAACTTG	78514
rs386868246	in-del	-/GAGCAGAATGGGAAGAGGAA			intron-variant	Arhgap10	Mm_Celera	8:77413203	GAATGGGAAGAGGAA[-/GAGCAGAATGGGAAGAGGAA]AGAGCAGAAAGGTGC	78514
rs386872478	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77432389	CAGGTTCCAGGGCTT[C/T]GGGTGGGAGGAGTGT	78514
rs386877553	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77306648	ACATATAAAGGCAGA[C/T]CTATCAGAATTGTAC	78514
rs386880797	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77387238	TGTGTGTGTGTGTGT[A/G]TGTATGTATGTATGT	78514
rs386881992	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77441913	GAGCTGCATTGTTCA[C/T]TGACTTAACTAGGTC	78514
rs386885844	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77425559	GAGAAGGAGGAGGAG[A/G]AGGAGGAGGAAGAGG	78514
rs386893762	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77418971	TTCTATAATTATATA[C/T]CAGTTGGGAATGGGG	78514
rs386897332	in-del	-/NN			intron-variant	Arhgap10	Mm_Celera	8:77285263	GCGTGCGTGCGTGTG[-/NN]TGTGTATACCAGATA	78514
rs386899167	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77381341	GCACCACTCACCAAG[A/G]GCTGGACTCCCCCAC	78514
rs386903104	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77503299	ATTATTATCCTTGGA[A/G]ATTTTAAAATTGTCC	78514
rs386905227	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77397398	CACTTTCCCCACATT[A/C]TAATAACCTTTCTTT	78514
rs386906741	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77374582	AAACCTAAATGTCTT[A/G]GGTTTTCTCCCGTAT	78514
rs386910998	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77382050	AAGCGTGCGCGCGCA[C/T]GCACACACACACACA	78514
rs386912068	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77413710	TCTCTATGAAACTAA[A/C]ATTAAATCTGTAGAA	78514
rs386915639	in-del	-/C			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503617	GGCTCCCCCATCCCC[-/C]GAGGGGGCTCTACCC	78514
rs386922966	in-del	-/AAAATGGCTTAGC			intron-variant	Arhgap10	Mm_Celera	8:77419091	TTCTAGTGGGCTGAA[-/AAAATGGCTTAGC]GAAATGTCTGCCATG	78514
rs386923544	in-del	-/AAA			intron-variant	Arhgap10	GRCm38.p3	8:77388338	TTCAATACACTTGTC[-/AAA]AAAAAAAAAAAAAAA	78514
rs386926331	in-del	-/TT			intron-variant	Arhgap10	Mm_Celera	8:77505047	ATTTCTTTTTTTTTT[-/TT]AAGATTTATTTATTT	78514
rs386927241	in-del	-/AAG			intron-variant	Arhgap10	GRCm38.p3	8:77370103	ATTCACAATCCTGAG[-/AAG]GGGGGGGGGGGCGGG	78514
rs386933237	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77412399	ACCTTTTTTTTTTTG[-/G]AGATGGGGGAGGAGG	78514
rs386938844	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77283299	GGCTGCCACTGTGGG[A/G]CCCCATGTTAGGTCA	78514
rs386940398	in-del	-/GTGT			intron-variant	Arhgap10	GRCm38.p3	8:77283968	TGTGTGTGTGTGTGT[-/GTGT]TCATTCAGGAACCCA	78514
rs386947075	in-del	-/TCTCTCTC			intron-variant	Arhgap10	Mm_Celera	8:77335985	CTCTCTCTTTCTCTC[-/TCTCTCTC]ACACACACACACACA	78514
rs386951446	in-del	-/CTGTGT			intron-variant	Arhgap10	Mm_Celera	8:77275210	TGTGTGTCCGTGCCT[-/CTGTGT]GTGTGTGTGTGTGTG	78514
rs386952584	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77419271	CCCATTCAATGAGAG[A/C]CTGTGTCTCAGAAGA	78514
rs386956649	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77482182	GTGCCACATCAAAAA[-/A]GGCCACCAGAAATTC	78514
rs386963006	in-del	-/CCAC			intron-variant	Arhgap10	Mm_Celera	8:77326350	ACTCCCAGCAACCAC[-/CCAC]ATGGTGACTCACAAC	78514
rs386967614	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77371908	CCCATGCCTACTTCC[-/C]AACCCAGCACGAGTT	78514
rs386970209	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77382367	CATCTACAAGCCGAG[A/G]GCACAGGCTAAGAGA	78514
rs386971967	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77422574	CTTTGTCTCCTGGGG[A/G]AAAACAAGCATTAAA	78514
rs386974686	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77321708	TTTAATGACGGCTGT[-/T]GAGGCTGCCTATGGA	78514
rs386974853	in-del	-/A			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77485408	GGGAGGAAGGCAAGA[-/A]TGCCTGTCCTGTGGA	78514
rs386976810	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77512454	TGAGACCTCGACTGC[A/G]GGGGAGGGGGAGGGG	78514
rs386977564	in-del	-/AGGC			intron-variant	Arhgap10	Mm_Celera	8:77416636	GACAGACTGGCAGGC[-/AGGC]GGGCGGGCAGGCGGA	78514
rs386978572	in-del	-/ACACACACACAGAGAGAGAGAG			intron-variant	Arhgap10	GRCm38.p3	8:77261041	CACACACACACACAC[-/ACACACACACAGAGAGAGAGAG]AGAGAGAGAGAGACA	78514
rs386984227	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77286916	CAGTTAAAAAAAAAA[-/A]CCCAAAATAACAATA	78514
rs386987803	in-del	-/AAGAAG			intron-variant	Arhgap10	GRCm38.p3	8:77363410	AAGAAGAAGAAGAAG[-/AAGAAG]CAGAAGAGGAGGAGG	78514
rs386989977	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77447544	TCTGTGGGGAAGACC[-/C]GCCAACAGTGCTCTG	78514
rs386990416	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77387122	AAGAAAGAAAGGAAG[A/G]AAGAAAGAAAGATTG	78514
rs386990961	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77449751	CAGAGCTCCATCCCC[-/C]TACTTCACAAAGTGA	78514
rs386992138	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77447088	GTGGTTGATTTTTTT[-/T]GTTTGTTTGTTTTGG	78514
rs387003260	in-del	-/AC			intron-variant	Arhgap10	Mm_Celera	8:77421050	CACACACACACACAC[-/AC]GCGCACGCATCCACA	78514
rs387003740	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77479161	GGAGGTTTCCAGTGT[C/T]AAAACTCCTTCTTAA	78514
rs387010001	in-del	-/CTCTCT			intron-variant	Arhgap10	Mm_Celera	8:77255573	TGTGCACGAGTCTCT[-/CTCTCT]GTGTGTGTGTGTGTG	78514
rs387010459	in-del	-/TGT			intron-variant	Arhgap10	Mm_Celera	8:77257741	GAGCACTTGAGCTGT[-/TGT]GCATTTGCAAAGGGA	78514
rs387013142	in-del	-/AATTGGCTTTGCATGGGTCC			intron-variant	Arhgap10	Mm_Celera	8:77419508	ATGGCACAGTTCGCC[-/AATTGGCTTTGCATGGGTCC]TGGGATTCGAACTCA	78514
rs387016109	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77413243	AGTCCCTCCTGGCTG[G/T]TGTTACCTCTAACCT	78514
rs387017099	in-del	-/C			utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250907	ATCAGTAGGACCCCC[-/C]ACGGCCGGGAGCTAC	78514
rs387024190	in-del	-/CTTTA			intron-variant	Arhgap10	Mm_Celera	8:77463783	TAACTTCTTTGGGTC[-/CTTTA]AGAGTTTTCAGAAAG	78514
rs387025095	in-del	-/GCAA			intron-variant	Arhgap10	Mm_Celera	8:77289050	CAAACAAACAAACAA[-/GCAA]ACACACACACCTACA	78514
rs387028330	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77426291	ACAGGTAAAATACAC[A/T]TTTAAAAGGGCAAAT	78514
rs387033501	in-del	-/GA			intron-variant	Arhgap10	Mm_Celera	8:77306864	CTACAAAGGATAACA[-/GA]TGGAAAACTCCAACA	78514
rs387040864	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77357020	ACCGCTTGCAGGGGG[-/G]CAGGGAGGACTGTAT	78514
rs387041480	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77400544	TGTGTATGCAGTACA[G/T]TATATATGCATGCCA	78514
rs387044611	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77387893	TCATGCCCCCCCCCC[-/C]AAGTCTTCCTAGGCC	78514
rs387045214	in-del	-/GACTAA			intron-variant	Arhgap10	Mm_Celera	8:77396506	GAAAGAAAAGACTAA[-/GACTAA]AATTAAATTTAGTGA	78514
rs387045904	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77497591	GTGTCCAAGACAGCA[C/T]ACAACATACCATGAA	78514
rs387049609	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77365409	AGTTATGAGACCATG[-/C]TGAGGCACAGCCTGA	78514
rs387051774	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77369301	TCAACTTAAAAAAAA[-/A]CTAAACCCCCAGATG	78514
rs387052689	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77422857	ACGCTGCTGCAACAG[C/T]CCTACTCTCCTCGTA	78514
rs387056704	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77383829	CTGCTGCGGGACATC[G/T]GTCAGCATCCGGGGC	78514
rs387059203	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77310113	ACGAATCACCAATCG[A/G]CTTTTGTGGGGCTCA	78514
rs387064544	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77448165	GGAAGTTGTGCGCAT[A/G]CGCGCGCGCACACAC	78514
rs387067436	snp	C/G			upstream-variant-2KB, downstream-variant-500B	Arhgap10, 0610038B21Rik	GRCm38.p3	8:77518889	TGATGGTAATAGTAC[C/G]AGGAAACTTCAAAGT	78514
rs387067849	snp	A/G			synonymous-codon, utr-variant-5-prime	Arhgap10	GRCm38.p3	8:77450898	TCTGAGCGAGTGAGC[A/G]AACTTCCTCTGGGCA	78514
rs387068530	in-del	-/TATG			intron-variant	Arhgap10	Mm_Celera	8:77457410	TGGAACAACAATATG[-/TATG]AACTAACCAGTACCC	78514
rs387069655	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77462194	CTAGCCAGGGATAGA[C/T]AGACCCCATCTCAAT	78514
rs387074331	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77369534	AATCTAAGCTAAAAA[-/A]GTTAAAGTATACAAA	78514
rs387075871	in-del	-/GAGA			intron-variant	Arhgap10	Mm_Celera	8:77489216	ATATACACACACAGA[-/GAGA]CATTCACATACATTC	78514
rs387075920	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77486002	GAAGTAGTAATAAAA[A/C]TAACTGTGTGCTTAG	78514
rs387083551	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77376807	GCCAGTTCACCTGGG[C/T]ACCTTACCACCCAAA	78514
rs387084495	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77425972	TTTTTCTGTGTAGCC[C/T]TGGCTGTCCTGGAAT	78514
rs387087990	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77404860	AGACCAGGCTGGCCT[C/T]GAACTCAGAAATCCG	78514
rs387093570	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77460153	CCCTGTCTAGAAAAA[-/A]CCCAAAGGAGTCGGG	78514
rs387096830	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77412725	TAGTGCAGGCGCTTT[-/A]CCAGCTAAGCAGCTT	78514
rs387097333	in-del	-/TGTGTGTG			intron-variant	Arhgap10	Mm_Celera	8:77326493	GTGTGTGTGTGTGTG[-/TGTGTGTG]GTGGAGTTCTTGGAA	78514
rs387102445	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77419440	CTGGTTGTTAGTGTC[A/G]CACTCACAGGCCAAC	78514
rs387105164	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77385991	CACAGGGAAGAAATC[C/T]GCTGTGCCTCACAGT	78514
rs387106872	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77472151	ATATATACACACACA[C/T]ATATATATATATACA	78514
rs387109021	in-del	-/CCCCCCCCCC			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	GRCm38.p3	8:77515760	AAAACTAGCCCCCCC[-/CCCCCCCCCC]ACACACACACACACA	78514
rs387110140	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77382168	CTTATTTAAAAAAAA[-/A]GAGAGAGAAATTCTA	78514
rs387111637	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77424444	TGCAGCAAGGACAGG[A/G]CAGAGCCCCACACCT	78514
rs387111962	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77459026	TCCCTCCTCCTCTTT[-/T]ATTTGCTCACCATAA	78514
rs387120339	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77418812	TCAGAAAACACAGAT[A/G]TTTGCATTAGGACTC	78514
rs387125731	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77432083	GGAGGAGAGGAGAGG[A/G]GAGGAGAGGGACAGA	78514
rs387128378	in-del	-/GCAGCA			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503731	AGAAAAGCTGGAGCA[-/GCAGCA]CAAACGGTGCAAAGC	78514
rs387131907	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77329131	TCCATTATGGATCAG[A/C]CAAGAACACAGGCAG	78514
rs387132285	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77481812	GAAGTCTCTATGTGA[-/A]TTTCCCAGAATTTCT	78514
rs387138011	in-del	-/AAAG			intron-variant	Arhgap10	Mm_Celera	8:77316276	ATTTACAAGTTTAAA[-/AAAG]AAAGAAAGAAAGAAA	78514
rs387144788	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77404518	TCCTTCCAAAAGCAA[-/A]TAAATCTAACCAAGC	78514
rs387154931	in-del	-/AC			intron-variant	Arhgap10	Mm_Celera	8:77475631	CACACACACACACAC[-/AC]TGTGAGACTTCATTG	78514
rs387161548	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77454759	TGACTTCATCTTGGT[A/G]GATGTATGTGTCCAG	78514
rs387163030	in-del	-/AACAAC			intron-variant	Arhgap10	GRCm38.p3	8:77414034	CACTCTTTCCAAGCT[-/AACAAC]AACAACAACAACAAC	78514
rs387163257	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77501026	GTCACAAGTCTTTAG[A/G]CATATGTGTATCTGT	78514
rs387164610	in-del	-/TGCATC			intron-variant	Arhgap10	Mm_Celera	8:77497374	AAAGAAAAAAACGTC[-/TGCATC]CACAGATACTAAGGC	78514
rs387170887	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77370204	TTCCTAGTGTTGGGG[A/G]TTGGAAGGGTTTAGA	78514
rs387173483	in-del	-/TAAT			intron-variant	Arhgap10	Mm_Celera	8:77370158	GACTCGGGAGTGAAT[-/TAAT]AGAGCACGGTACAGA	78514
rs387177220	in-del	-/GAGG			intron-variant	Arhgap10	Mm_Celera	8:77462271	AGGGAGGGAGGGAGG[-/GAGG]AAGAAAGGGTGGGTC	78514
rs387179608	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77368461	ACCAACACCCTTACC[-/C]TTTTCACTGGTGCAG	78514
rs387180719	snp	A/C			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	GRCm38.p3	8:77515521	AACTTTAATGTGCCA[A/C]GTGGGAAAAGGCCAG	78514
rs387183491	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77406693	GAGGAGTTTGCACTG[-/T]ATGTGGAAGGAAAGG	78514
rs387185890	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77313732	GCGGGTGGTCAGGGG[-/G]AGTTTAGCAGCTAAA	78514
rs387190248	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77252453	CTATTCTTAAAGGTT[-/C]TATCCATACATTGTA	78514
rs387193182	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77385330	CTCAGGCTGTAACAT[A/G]CTCTATAAGACACGA	78514
rs387194040	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77430069	GAAAGAAATGTTTTT[-/T]AAAATGTGACTGCAA	78514
rs387202084	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77423411	GAGGTGGGTTCCGGG[A/G]GTTGGGGGTCTGAGG	78514
rs387206427	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77429896	CTTTATAACTAAAAT[G/T]AAAGTAACAGGATTA	78514
rs387211560	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77270619	AGTATGAAATCCCAC[C/T]CTCAGCTGAAGTGCC	78514
rs387212082	in-del	-/GT			intron-variant	Arhgap10	Mm_Celera	8:77274233	TGTGTGTGTGTGTGT[-/GT]AAGAGAGGGAGAAGG	78514
rs387215201	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77432517	GAGGAAAACAGGGCA[A/G]TCTCCAAGGCCAGGT	78514
rs387216841	in-del	-/TTAC			intron-variant	Arhgap10	Mm_Celera	8:77444174	AAACTGAATCCTCAC[-/TTAC]AGGCTGGCAAGAAAA	78514
rs387217518	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77277475	TTGTTTGAAAAAAAA[-/A]CAAAACAAAACAAAG	78514
rs387220785	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77425528	AGAGGACAAGGAGGA[C/G]AAGGAGGAGGAGGAG	78514
rs387233492	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77386681	GGCTCACAACCATCT[A/G]TACAGCTTCAGTGTA	78514
rs387234696	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77322491	GAAGCAACAGCCTCC[A/T]TATGGAGGGCAGGTG	78514
rs387234851	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77327883	TTTTTTTTTTTTTAA[-/A]TTCCTACTTGGATCT	78514
rs387235004	in-del	-/CCAG			utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250915	ACCCCCCACGGCCGG[-/CCAG]GAGCTACAGGAGCTT	78514
rs387242458	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77420295	CCACCTCCCTGTCTG[C/T]CACGTCCTGAAATGA	78514
rs387243986	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77373071	AATGGTCTTTTTTTT[-/T]GGGAAGGGCAGAAGA	78514
rs387245386	in-del	-/CGCCAGTCACGCTC			utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250739	AACTGACTCCAGCAA[-/CGCCAGTCACGCTC]TGCTTCCGCCCACAT	78514
rs387248723	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	GRCm38.p3	8:77516968	AATTTCCTACTCACA[A/G]GCACTTCTCGCAGGC	78514
rs387252214	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77413645	AAAAAGAAAAAAAAA[-/A]TACAGATTCCAACAT	78514
rs387252977	in-del	-/CAGAGCC			intron-variant	Arhgap10	Mm_Celera	8:77260959	TGCTGGGTTGAAACC[-/CAGAGCC]TTGCACTTGCTCAGG	78514
rs387254299	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77418978	ATTATATACCAGTTG[A/G]GAATGGGGATCAGTC	78514
rs387256029	in-del	-/GGGAGGAACATTCTGAAGGAAT			intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77492834	GCCTTGCCACTAGCT[-/GGGAGGAACATTCTGAAGGAAT]CACTCTCCACACTTC	78514
rs387256092	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77334424	AGAGTGGAGCAGCGC[A/G]GAGAGAGAGAGAAGG	78514
rs387256760	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77480753	TCCTGTAAGAACAAA[-/A]GGTTCATAACTACTG	78514
rs387259196	in-del	-/CAA			intron-variant	Arhgap10	Mm_Celera	8:77324980	CAGAGGTCAGGCCAA[-/CAA]TGCACTGTAATGCAT	78514
rs387260657	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77410425	TACCCCAGACACCAA[C/T]GTTCACCTTAAGCAA	78514
rs387261523	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77387131	AGGAAGGAAGAAAGA[A/T]AGATTGATTCAATTC	78514
rs387266301	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77413370	CAGGAATGTGTGCAC[C/G]CTGTGCCTTCAGGGG	78514
rs387270404	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77287117	CTGTATAAGTAAAAA[-/A]TCTACCCTCAAATAC	78514
rs387275145	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77447610	CTCACCTACAGCTCC[-/C]GCCCGTCTGCTCTCA	78514
rs387281704	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77511659	GAGTCTCGGCCGGGC[A/G]TGGTGGCGCACGCCT	78514
rs387287602	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77508695	TTTGTTTTTTTTTTT[-/T]AAATATTTGGTGTGA	78514
rs387287901	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77413935	GGGGGGGGGGGGTGT[A/T]ATAAAAGGTGTTCGA	78514
rs387289187	in-del	-/GTGTGTGT			intron-variant	Arhgap10	Mm_Celera	8:77445991	TGTGTGTGTGTGTGT[-/GTGTGTGT]CTTTCTTCCAGGAAC	78514
rs387291742	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77431079	CTGAACTGAGTGTCT[A/T]GGAAGCAGAGACACA	78514
rs387303859	in-del	-/GACACAGACACA			intron-variant	Arhgap10	Mm_Celera	8:77377827	ACAGACACAGACACA[-/GACACAGACACA]CACACACACACACAC	78514
rs387304096	snp	A/T			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77484704	TGGTACACGCCTTTA[A/T]TCCCAGCATTTAAGA	78514
rs387311619	in-del	-/GG			intron-variant	Arhgap10	GRCm38.p3	8:77483271	ACACACACACACACG[-/GG]AGGGGAAGGGGGAGA	78514
rs387313433	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77443777	CTGAGTTCGAGGTCA[A/G]CCTGGTCTACAGAGT	78514
rs387315144	in-del	-/GAACGTAGGCGCAC			intron-variant	Arhgap10	Mm_Celera	8:77251857	TTTTATACTAGAAAT[-/GAACGTAGGCGCAC]ACATACACCCCTGGT	78514
rs387326409	in-del	-/ACACAC			intron-variant	Arhgap10	Mm_Celera	8:77284091	CACACACACACACAC[-/ACACAC]GTTTACCCATCCATT	78514
rs387329570	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77388444	GTCAAGAAAAAAAAA[-/A]TCAGAACTGGAAATG	78514
rs387330898	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77344827	TAGAAAGAAAAAAAA[-/A]GTCTTAGTTGGGTGG	78514
rs387331757	in-del	-/AAAAAAAGG			intron-variant	Arhgap10	Mm_Celera	8:77287915	GAAAGAGAAAGAGAA[-/AAAAAAAGG]AAAGAGAAAGAGAAA	78514
rs387332739	snp	A/G			upstream-variant-2KB, nc-transcript-variant	Arhgap10, 0610038B21Rik	GRCm38.p3	8:77518288	GCCTCGGTCCCCGAG[A/G]TCAGACGACTTAAAA	78514
rs387335445	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77502962	TCTTCAACAGGAGCC[A/G]GGCTGCATCTGGATA	78514
rs387339455	in-del	-/TTTTTTTTTT			intron-variant	Arhgap10	Mm_Celera	8:77425931	TTTTTTTTTTTTTTT[-/TTTTTTTTTT]AAGTTTTCAAGAAGC	78514
rs387339710	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77366673	TGTGTGGGTAAGGGT[A/G]TGGAGGCTCTGAACT	78514
rs387346246	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77418948	CTAAGAAAAAAAAAA[-/AA]GGTTAATTCTATAAT	78514
rs387350452	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77387242	TGTGTGTGTGTATGT[A/G]TGTATGTATGTATGT	78514
rs387354081	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77421772	GAAAGCAGTGGTTGG[C/T]TCACGTGACGCTCAT	78514
rs387359541	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77410430	CAGACACCAATGTTC[A/G]CCTTAAGCAATCTCT	78514
rs387360266	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77412669	ACCTCAACTTTTTGA[A/C]GGGTGCTGAGGATCT	78514
rs387360448	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77425814	TCTAAGAGACAGAGT[A/G]TAGGCTCACACAGTC	78514
rs387362864	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77491427	GTCACTGGTCTGGTT[C/T]GAGGCCTCTGGCTCC	78514
rs387365198	in-del	-/CTCTCTCTCTCTTTCT			intron-variant	Arhgap10	Mm_Celera	8:77495335	TCTCTCTCTCTCTCT[-/CTCTCTCTCTCTTTCT]TTCTTTCTTTCCTTT	78514
rs387365826	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77259848	TAATAATAATAATAA[-/A]TAAATAAATCTTTAA	78514
rs387368688	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77423937	GCAAGTGCATGACAC[A/G]TGAGGTCCTGGGCAG	78514
rs387377568	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77365603	ATCGAAATGAATAAA[G/T]AATTCAACTTAATGT	78514
rs387382604	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77471352	ATTGGAGGGGTCACA[C/T]GACCCCTAATGGAGG	78514
rs387384069	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77328299	TACATCTGCGGTTTG[C/T]CCTTCCAGTTGTTTC	78514
rs387384177	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77397801	TCACCTGAGAACTGA[A/G]CCTCTGGGCACGCCA	78514
rs387389282	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77511637	GTTTTATTTTTTTTT[-/T]AGGACAGAGTCTCGG	78514
rs387395015	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77417681	TAAGATGAAAAAAAA[A/G]AGAGAGAGAGAGAAT	78514
rs387404041	in-del	-/AA			upstream-variant-2KB, nc-transcript-variant	Arhgap10, 0610038B21Rik	Mm_Celera	8:77518302	GATCAGACGACTTAA[-/AA]GTCGGGGCGGGTGGA	78514
rs387410275	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77447263	GACTCTGCAGACACA[A/G]TCCTATTCTCACATC	78514
rs387414367	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77328531	TTAGTTAAATGTAGT[A/T]AAATGTAAATGTCAG	78514
rs387415736	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77386235	CGGGTTATTAAAAAA[-/A]GGGATTAAAGGATTA	78514
rs387419757	in-del	-/CGTGTGTGTG			intron-variant	Arhgap10	Mm_Celera	8:77433368	GGACATGTGCACGCA[-/CGTGTGTGTG]TGTGTGTGTGTGTGT	78514
rs387423499	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77506151	TACTTTTATGAAGTG[A/C]TGTGGCTTGTGAAGG	78514
rs387426843	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77365437	TGATGTAGTGCCTAC[A/G]GGTGCACTTCCATGG	78514
rs387427021	in-del	-/AC			intron-variant	Arhgap10	Mm_Celera	8:77382102	CACACACACACACAC[-/AC]TCACACACACACATT	78514
rs387427479	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77412743	GCTAAGCAGCTTCCC[-/C]AGGCCACAGCAGGCT	78514
rs387430998	in-del	-/CTTAACTTCCTCTTCCGTAA			intron-variant	Arhgap10	Mm_Celera	8:77454351	TACCAAGTGTGACAA[-/CTTAACTTCCTCTTCCGTAA]GTTGAATGTCTTGCT	78514
rs387434841	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77400686	GCTCTTAACTGCTGC[A/G]CCGTCTCTTCAGCCC	78514
rs387438405	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77419389	CCCTACCATCGGAAC[A/G]ATGTTGAAGTGGACT	78514
rs387442951	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77499891	ACAATCATGGGGGAG[A/G]GAGAGGGACACCCTA	78514
rs387443360	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77448167	AAGTTGTGCGCATGC[A/G]CGCGCGCACACACAC	78514
rs387443622	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77368852	TTTTGCTTTCTGTTC[C/T]TGTTTTTATTTTTTA	78514
rs387445445	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77422866	CAACAGCCCTACTCT[C/T]CTCGTATCAACAAGA	78514
rs387449476	in-del	-/TT			intron-variant	Arhgap10	GRCm38.p3	8:77327867	TTATATCTTCCAGGG[-/TT]TTTTTTTTTTTTTAA	78514
rs387452840	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77295626	GGGAGTGGGGGGGGG[-/G]AGGGTATGAGGGACT	78514
rs387454623	in-del	-/GAAA			intron-variant	Arhgap10	Mm_Celera	8:77316295	AAAGAAAGAAAGAAA[-/GAAA]AAACAAATTTTGTTA	78514
rs387455859	in-del	-/CACACACA			intron-variant	Arhgap10	GRCm38.p3	8:77467663	ATTACTACAGAAATT[-/CACACACA]CACACACACACACAC	78514
rs387459813	in-del	-/AGGTATCC			intron-variant	Arhgap10	Mm_Celera	8:77459600	TGGCCTTGAACTCAC[-/AGGTATCC]TCCTACCTCAGTCTC	78514
rs387468430	in-del	-/G			intron-variant	Arhgap10	GRCm38.p3	8:77283190	GGGAGGGGGAGGGGG[-/G]AGGGAGGAGGGAAGG	78514
rs387472498	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77501343	AGTCCAAACACTGCT[A/G]TGTTGCTGGACCAGT	78514
rs387474243	in-del	-/GCTATTG			intron-variant	Arhgap10	GRCm38.p3	8:77255705	GGGCCTCCTGGGTTG[-/GCTATTG]GCTATCTTCTGGCCT	78514
rs387476754	in-del	-/AC			intron-variant	Arhgap10	Mm_Celera	8:77405331	ATGTACATCCATCAC[-/AC]TCATACCCAAACCGC	78514
rs387477523	in-del	-/GTCTGTCT			intron-variant	Arhgap10	GRCm38.p3	8:77255603	TGTGTCTGTCTGTCT[-/GTCTGTCT]ACCTATGTATGAGTA	78514
rs387485845	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77420002	TCTTAATAAGATTTT[-/T]GAGACCAGAGTAGAA	78514
rs387489208	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77427346	GCCGCTGCTCAGCTA[A/G]GTAAACTCTAGCCTC	78514
rs387492506	snp	A/T			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	GRCm38.p3	8:77515713	AAAACACAAGTCACA[A/T]ATTCCAGAAGGTCTA	78514
rs387493120	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77413461	CTCACAACCACCCGA[A/C]TCTTCAGATCGAAGG	78514
rs387498667	in-del	-/AA			intron-variant	Arhgap10	GRCm38.p3	8:77445303	GAAAGAAAGAAAGAA[-/AA]AAAGAAAGAAAGAAA	78514
rs387507037	in-del	-/TTTTT			intron-variant	Arhgap10	Mm_Celera	8:77447051	TTTTGGTTTGGTTTG[-/TTTTT]GTTTAAGGGGGGGAG	78514
rs387516676	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77357235	ATATATCTGCAAAAA[-/A]CTCTTTTTAGTATCA	78514
rs387518170	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77412484	CTGTAGACCAGGCTG[G/T]CCTGGAACTCACAGA	78514
rs387519893	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77336990	CAAAAACCAGGTTCA[A/G]ATGTCGGCTCAGCCA	78514
rs387522731	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77487849	TCTCCAAGCCTTTGG[-/G]TCAACATGAGGACAA	78514
rs387523705	in-del	-/CACA			intron-variant	Arhgap10	Mm_Celera	8:77467708	ACACACACACACACA[-/CACA]AAGGCTGATCTCTTC	78514
rs387524975	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77431139	GTGCACGCACCCCCC[-/C]TAAACTGCAAGTTCT	78514
rs387527025	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77396850	AATGAATCAGAAACA[-/A]GGGAATGAGCTGTCC	78514
rs387527898	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77449419	CCTGTGCACACTGCC[A/G]CATCCCTAGCCTTCT	78514
rs387529229	in-del	-/TG			intron-variant	Arhgap10	Mm_Celera	8:77413679	TGATTTTTTTGTGTG[-/TG]CATACATTTTGATGT	78514
rs387535733	in-del	-/GAGTGAGCACGCGC			intron-variant	Arhgap10	Mm_Celera	8:77489299	TGTGCGCGCGTGCAC[-/GAGTGAGCACGCGC]ATGAGCGTGCATGTG	78514
rs387541720	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77371836	CAAGTAACTGCACAC[A/G]GGAAAGAGGCAGTCT	78514
rs387549413	in-del	-/AAA			intron-variant	Arhgap10	Mm_Celera	8:77308038	CAAACAAAAAAAAAA[-/AAA]CTATACAAAGAATCA	78514
rs387550481	in-del	-/GC			intron-variant	Arhgap10	Mm_Celera	8:77324992	CCAATGCACTGTAAT[-/GC]ATGGGTTTGTGAACA	78514
rs387557062	in-del	-/CAA			intron-variant	Arhgap10	GRCm38.p3	8:77457636	ACCCAATAATAATAA[-/CAA]TAATAATAATAACTA	78514
rs387565363	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77369767	CCCACATAGCACGAC[-/C]TGTCCCACAGTCTGC	78514
rs387566831	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77404623	ACGAAGCCTCTCCTG[C/T]AATGCCACTTCTTCT	78514
rs387570729	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77486015	AAATAACTGTGTGCT[C/T]AGGGGGTCACCAGAA	78514
rs387570772	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77365644	GTTGAAACCTGAAAA[-/A]CCTTGAACACAAAAG	78514
rs387571027	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77447717	CAGGCACTCTGACGT[G/T]TGTCTTCGTGAGAAG	78514
rs387571808	in-del	-/GC			intron-variant	Arhgap10	Mm_Celera	8:77370722	ATGGTAATGACCCGC[-/GC]AGCCCTCCCATAGCT	78514
rs387580493	in-del	-/C			utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250903	CACGATCAGTAGGAC[-/C]CCCCACGGCCGGGAG	78514
rs387583787	snp	A/T			intron-variant	Arhgap10	Mm_Celera	8:77322492	AAGCAACAGCCTCCT[A/T]ATGGAGGGCAGGTGA	78514
rs387585328	in-del	-/GCAC			intron-variant	Arhgap10	GRCm38.p3	8:77373449	CAGACCTGGGCTAAC[-/GCAC]CACAGACCTGGGCTT	78514
rs387586811	in-del	-/TT			intron-variant	Arhgap10	Mm_Celera	8:77498833	TCTTTTTTTTTTTTT[-/TT]AACTTTTTTTGAAAG	78514
rs387592337	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77387118	AAGAAAGAAAGAAAG[A/G]AAGGAAGAAAGAAAG	78514
rs387592419	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77446528	AGTCACTGCATGGGG[-/G]TAATGCATGCCTACA	78514
rs387593245	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77350654	CCCATTGGGATTGCT[A/G]TAAGTTTTTCAACAG	78514
rs387594819	snp	A/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77381973	TAACATTAAAAAAAA[A/G/T]GGGGGGGGCCTTTAA	78514
rs387599644	in-del	-/CCCACCCTCACT			intron-variant	Arhgap10	Mm_Celera	8:77326649	TGACCATTGCTTTCT[-/CCCACCCTCACT]AATCTGATAACTGTA	78514
rs387601321	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77397813	TGAGCCTCTGGGCAC[A/G]CCAGTGAAGGGCTGC	78514
rs387602342	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77420930	AGGACATACAGAAAA[G/T]TCTTCCCAAACTCTA	78514
rs387612994	in-del	-/GAG			intron-variant	Arhgap10	Mm_Celera	8:77483395	GAGAAGGACTGAGAG[-/GAG]AAGGGCAGAATATTA	78514
rs387615031	in-del	-/CT			intron-variant	Arhgap10	Mm_Celera	8:77328436	CTGCTTTGAGCGTCT[-/CT]GTTTTCTTAGTTTTA	78514
rs387616801	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77425342	TGCTTGCATACTGAG[A/G]AGGAGGAGGAGGAGA	78514
rs387617141	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77419397	TCGGAACAATGTTGA[A/G]GTGGACTGGAACACA	78514
rs387624582	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77325526	ACAGAAAACTGCCCC[-/C]TTGCCATAGTCTATT	78514
rs387636166	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77450149	GTGTAACTGGAAAAG[A/G]CACACAAACTTACAA	78514
rs387643584	in-del	-/TA			intron-variant	Arhgap10	Mm_Celera	8:77275160	AAGCATTTATCTGTA[-/TA]GCAAAGATAATCTGA	78514
rs387650255	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77497112	CAGAAGGACTATTTT[-/T]CATGAGTGTGATTTT	78514
rs387652401	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77445288	AGAAAGAAAGAAAGA[-/A]GAAAGAAAGAAAGAA	78514
rs387655265	in-del	-/T			intron-variant	Arhgap10	GRCm38.p3	8:77387175	CTTCTATTTTTTTTT[-/T]AGTTTTTTTTTAATA	78514
rs387661596	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77503660	ACCGCCACCACCCCA[A/G]GGCCTCCCTGGCCTC	78514
rs387662911	in-del	-/TCAG			intron-variant	Arhgap10	Mm_Celera	8:77395685	CAAGTTTCCTCTCAG[-/TCAG]AACACGCATCACCAA	78514
rs387663572	in-del	-/TG			intron-variant	Arhgap10	Mm_Celera	8:77419309	ACTGAGAGAGGCAAC[-/TG]AGAGAGACAGAAGTG	78514
rs387668071	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77397390	AACAGGTCCACTTTC[C/T]CCACATTCTAATAAC	78514
rs387669965	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77447350	TAGCTGCCTCCAAAG[A/C]CGAAGATTAAATCAC	78514
rs387673330	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77413702	TTTTGATGTCTCTAT[A/G]AAACTAAAATTAAAT	78514
rs387674325	in-del	-/GTGTGT			intron-variant	Arhgap10	Mm_Celera	8:77274189	AAAATCAAATGATTG[-/GTGTGT]GTGTGTGTGTGTGTG	78514
rs387676385	in-del	-/CAAT			utr-variant-3-prime	Arhgap10	Mm_Celera	8:77250700	ATTAAACATCACAAT[-/CAAT]GCCCAGTCCTGCTAG	78514
rs387676914	in-del	-/C			intron-variant, upstream-variant-2KB	Arhgap10	Mm_Celera	8:77503981	ATGAGCCCCCCCCCC[-/C]TCCAGCAACTGTTAA	78514
rs387677912	in-del	-/TAAC			intron-variant	Arhgap10	Mm_Celera	8:77429050	GATGTAAACACTAAC[-/TAAC]ATCCATGTTTGAGGA	78514
rs387677988	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77508850	CTATCTACTTAAGAT[A/G]TAATAATAATAAAAT	78514
rs387678862	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77509026	TGTGTGTGTATAAAA[-/A]TCAATGATAGTTTTG	78514
rs387680641	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77333156	TGTATATCTGTGCAC[C/T]ATATGAGTGCATGTT	78514
rs387682965	in-del	-/AACT			intron-variant	Arhgap10	Mm_Celera	8:77413126	TAGGCACTCAACTCT[-/AACT]GCTGAATCATCCCTC	78514
rs387691705	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77401931	CGTCGTCGTGGCCTC[C/T]TCCTCCTCCTCCCTC	78514
rs387709121	in-del	-/GATC			intron-variant	Arhgap10	GRCm38.p3	8:77489134	CTGTCTCAATCTATC[-/GATC]AATCAATCAATCAAT	78514
rs387710139	in-del	-/GT			intron-variant	Arhgap10	Mm_Celera	8:77347990	TGTGTGTGTGTGTGT[-/GT]CTGTGTGTCTGCCTT	78514
rs387718878	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77433397	GTGTGTGTGTGTGTG[C/T]ATGTCCCTTCTCTTG	78514
rs387719631	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77365803	AGGTGAGAAAATGTC[C/T]GTGTTTTAAATTGGC	78514
rs387721183	in-del	-/ACACTC			intron-variant	Arhgap10	Mm_Celera	8:77288475	CACACACACACACAC[-/ACACTC]TGCTTTCTTCCAAGT	78514
rs387721604	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77396035	ACAGCCTCTGCAAAT[A/G]GGAAGCATCAAAATG	78514
rs387723073	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	GRCm38.p3	8:77515518	GACAACTTTAATGTG[C/T]CAAGTGGGAAAAGGC	78514
rs387730094	in-del	-/ACAA			intron-variant	Arhgap10	Mm_Celera	8:77455329	CCCCCTTGTCAGTGA[-/ACAA]TCAAGAAATGAGCCG	78514
rs387739355	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77263046	TCCAGGCACGGCCCA[-/A]TGGTACAATTCACCT	78514
rs387740788	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77297843	TGACTTTTTTTTTTT[-/T]CTTTCCTATTTTGTC	78514
rs387743847	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77449449	TTACATGGGTTGGGG[-/G]AAGCCAAACTTGAAT	78514
rs387745598	in-del	-/AGGGAAGAATGC			intron-variant	Arhgap10	Mm_Celera	8:77260779	GGCAGGAACTCAAGC[-/AGGGAAGAATGC]TGCTCACGACTTGCT	78514
rs387749571	in-del	-/GAAAG			intron-variant	Arhgap10	Mm_Celera	8:77365665	ACACAAAAGACAAAG[-/GAAAG]AGAAGTTACTCTCCA	78514
rs387750068	in-del	-/TAAATAAATAAATAAATAAA			intron-variant	Arhgap10	Mm_Celera	8:77320379	AAATAAATAAATAAA[-/TAAATAAATAAATAAATAAA]AGCATAATTTGCTCT	78514
rs387758360	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77329485	CTATGAAGTTGAGGC[C/T]GTCTGTGAAGTCTCA	78514
rs387760093	in-del	-/TCTCTC			intron-variant, downstream-variant-500B	Arhgap10	Mm_Celera	8:77358130	CTCTCTCTCTCTCTC[-/TCTCTC]AAAATGCCATCTCAG	78514
rs387766847	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77369362	GACCTATACTTTACC[-/C]ATGGGTTTCTCCTCC	78514
rs387770710	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77412631	ACATCAGCACAGCAC[A/G]AGCATGGGATACTCG	78514
rs387772930	in-del	-/CACAA			intron-variant	Arhgap10	Mm_Celera	8:77406669	TGAGAGAGACATCAA[-/CACAA]TGGCTTTCTGAGGAG	78514
rs387778862	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77511802	ACAAACCAAAAAAAA[A/C]AAAAACAAAAAAAGA	78514
rs387783490	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77425547	GAGGAGGAGGAGGAG[A/G]AGGAGGAGGAGGAGG	78514
rs387788244	in-del	-/GCACTT			intron-variant	Arhgap10	Mm_Celera	8:77488790	GTCACGTGTTCAATT[-/GCACTT]TTCTGTACATCGGTT	78514
rs387797088	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77330087	TTCCTTTATGTCAAC[A/C]GTTGCTGGGCAAGGT	78514
rs387808308	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77286223	GCAAGAAGAAAAAAA[-/A]GACCTGCAATCAGGC	78514
rs387812177	in-del	-/TTTT			intron-variant, utr-variant-5-prime	Arhgap10	Mm_Celera	8:77492421	TAGGTTGTTTTTTTT[-/TTTT]ACCTCTCAATTACGT	78514
rs387814957	in-del	-/T			intron-variant	Arhgap10	Mm_Celera	8:77447501	GGTCACATAGTTTTT[-/T]CCATAAAAGTCCCAA	78514
rs387815006	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77491295	ATCTTAAAAAAAAAA[C/T]TAAATAAACAAAGAT	78514
rs387815518	in-del	-/TCT			intron-variant	Arhgap10	Mm_Celera	8:77513458	GAGAACTGAACTTCT[-/TCT]CGTTCTTCCAAATCG	78514
rs387819316	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77412705	CGGATCCTCAGGCTT[A/G]TTTGTAGTGCAGGCG	78514
rs387821373	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77503548	CAGGAAACCTGCTGG[C/T]GCCTGCTGAGACAGA	78514
rs387830198	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77365469	TTTGTTTATTTATTT[A/G]CTTGGGTTTTTTTTT	78514
rs387830638	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77419110	TGTCTGCCATGCAAA[-/A]TATAGAGCTGTGAGT	78514
rs387832167	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77380704	CAAAACAAAAAAAAA[-/A]CCTCAAAGCCCTGTG	78514
rs387835278	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77419241	AACCAACCAGCCCAC[A/T]CAATTGGTGAGCCTC	78514
rs387846445	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77419760	AATGAAAAACCATGA[A/C]TGACGGTCAGTCAGG	78514
rs387848717	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77433936	CCCCTCAAACACAAG[A/G]GCTCCTGTATGCCAT	78514
rs387853174	in-del	-/A			intron-variant	Arhgap10	Mm_Celera	8:77312939	TTTCAGAAAAAAAAA[-/A]TGGCACTAGACACAC	78514
rs387854303	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77333130	TTGTGTGTCTGTATG[A/T]TTTGTCCACGTGTAT	78514
rs387854730	in-del	-/CACA			intron-variant	Arhgap10	Mm_Celera	8:77457890	AGCGCACATGCATGA[-/CACA]TACACACAAAGATAA	78514
rs387860940	in-del	-/GA			intron-variant	Arhgap10	Mm_Celera	8:77263229	AAATAGTGGAGAAAA[-/GA]AAATCTCCCAGGAGA	78514
rs387862595	in-del	-/GTGT			intron-variant	Arhgap10	GRCm38.p3	8:77443994	TGTGTGTGTGTGTGT[-/GTGT]AATACATAAAGGTGA	78514
rs387868458	in-del	-/ACCT			intron-variant	Arhgap10	Mm_Celera	8:77460348	AAAGAATATGAAGAT[-/ACCT]TACAAATACCTTGAT	78514
rs387869766	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77401964	CCCCTCCTCCTCCTC[C/T]TCTTCCTCCTCCTCC	78514
rs387880890	in-del	-/GT			intron-variant	Arhgap10	GRCm38.p3	8:77424288	GGGGGGAGGGGGGGG[-/GT]CATGCACTGCAGGGC	78514
rs387881687	snp	A/G			intron-variant	Arhgap10	Mm_Celera	8:77445587	GGGAAGGGGAAAGGA[A/G]GGGAGGGGAGGGGAG	78514
rs387881902	in-del	-/TGGCTAT			intron-variant	Arhgap10	Mm_Celera	8:77255710	TCCTGGGTTGGCTAT[-/TGGCTAT]CTTCTGGCCTTTCTT	78514
rs387883050	in-del	-/G			intron-variant	Arhgap10	Mm_Celera	8:77420473	CGGTATGGCGGGGGG[-/G]CTGTGCCCCTCACTG	78514
rs387883475	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77328332	TGACAACTGAAGGAG[C/G]ATGTGTTCATGGCAG	78514
rs387886726	in-del	-/C			intron-variant	Arhgap10	Mm_Celera	8:77480749	GTCTCCTGTAAGAAC[-/C]AAAGGTTCATAACTA	78514
rs387889636	snp	C/G			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77503956	CAGCCCTAAGGATGT[C/G]GGAACCCTCATGAGC	78514
rs387889882	in-del	-/TTGGGGTACACATGGCTGTCTC			intron-variant	Arhgap10	Mm_Celera	8:77446951	GCCTGTGGCTGTCTG[-/TTGGGGTACACATGGCTGTCTC]CTGGGGTGCCTGTGG	78514
rs387891047	in-del	-/AA			intron-variant	Arhgap10	Mm_Celera	8:77400101	GAACTGAGACAGGAA[-/AA]GAGTTTAACCGAAGC	78514
rs578280732	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77308220	AATCAGATCCTACTA[C/T]AAAAGCCTATATTCA	78514
rs578288605	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77411581	ACACACGCACATGCA[C/T]ACACACACACACACA	78514
rs578298114	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77306453	AATAAATATCTTCAA[C/T]AAAATTATAGAAGAA	78514
rs578306126	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77280133	CTCCAACCAGGGAAA[C/T]AGCTGTGGTGAGAAG	78514
rs578312437	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77300298	GAAAAAAATGTTCAA[C/T]ATCCTTAATCATCAG	78514
rs578329921	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77295847	AAATGTGCCCACAGG[A/G]TAGTCTCTATAAAAA	78514
rs578333534	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77261080	AGAGAGAGAGACAGA[C/G]AGAGAGAGAGAGAGA	78514
rs578360505	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77502645	CTCAGAAACCAGCCA[A/G]CAACAGGCTAAACAC	78514
rs578361041	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77499015	CGCTGCCCGCTGCCC[G/T]CTGCCTCTGCCTCTG	78514
rs578375598	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77472158	CACACACATATATAT[A/G]TATATACACATATAT	78514
rs578379398	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77456810	TCAACAGAGGAATGG[A/G]TACAGAAAATGTGGT	78514
rs578381599	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77443928	GAATAAAAACCAAGT[A/G]TCAAACACCAAAGTG	78514
rs578390030	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77511496	AGAGAGAGAGAGAGA[A/G]AGAGAGAAAAGAAGA	78514
rs578393927	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77449362	CTGGCCCTGTGCACA[C/T]TGCCGCATCCCTGGC	78514
rs578406941	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77493199	GGAGGAGGAAGAGGA[A/G]AGAAGAGGAAAAAGA	78514
rs578414076	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77252956	TTCTGGAGATGGCTT[G/T]CTTACACGCCTATCT	78514
rs578431946	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77305364	GGACTTTTGGGATAG[C/T]ATTTCAAATGTAAAT	78514
rs578479614	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77438540	TTAAGGAGCTGAGCT[A/G]GTAAAAGAATTGAAT	78514
rs578492351	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77421404	GGAAGTCACGGCTTC[A/C]CAGTCAGGGCTTCTG	78514
rs578496320	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77467481	ACAGAGAAGAACCCC[A/G]TCTTCAAAAACCATT	78514
rs578498824	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77410321	TATTTCTGAATTCAC[C/T]TAAGCAAAATGTCAC	78514
rs578498873	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77261088	AGACAGAGAGAGAGA[C/G]AGAGAGACAGACAGA	78514
rs578518986	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77335417	GTCAGAGGACACCCC[G/T]TCTCCCTGGCCTTCC	78514
rs578527189	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77369185	GACCAGGCTGGCCTC[A/G]AACTCAGAAATCCAC	78514
rs578532679	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77451517	CCCATCGCCTCCATT[C/T]TCCATGGCAGGTCAT	78514
rs578535247	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77387054	AAGGAAGGAAGGAAG[A/G]AAGAAAGAAAGAAAG	78514
rs578548387	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77375062	ACAGCAGTCACACAC[A/G]TGGCCAGGAACGTCT	78514
rs578549791	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77299582	GAGGAGAAAGTGGGG[A/G]AAAGCCTCGAAGATA	78514
rs578571645	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77345692	AGCTCAGGACTTCCC[C/G]CTACAAGAGATGGCC	78514
rs578595729	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77511515	GAGAAAAGAAGAAAG[A/G]CAGGCAGGCTACGAA	78514
rs578596262	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77472527	CTGAAGACAGCTACA[A/G]TGTACTCATTCATTC	78514
rs578610816	snp	A/T			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77493372	CCCTTCCTCCTTCAC[A/T]GGCCTACAGGAACAC	78514
rs578620396	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77305967	ATTTAAAATCACATC[G/T]CATGATGATGATAAA	78514
rs578624514	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77318694	GGACCTGAGTCCCTC[A/G]TCAGTTGGGAACGCT	78514
rs578632743	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77347399	TTGTTGTTGTTGTTG[A/T]TGTTGTTGTTGTTGT	78514
rs578647353	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77253588	ACACAGAGAGCTCGG[C/T]TTCAGCTCTGAAAGT	78514
rs578653533	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77287900	AAGGAAGGAAGGAAG[A/G]GAAAGAGAAAGAGAA	78514
rs578697701	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77496596	CCCAAAGACAAATTG[C/T]CTTATTTTTTAAAAA	78514
rs578702847	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77452356	CGAGACAGGGTTTCT[C/T]TGTGTAGCCCTGGCT	78514
rs578713480	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77441325	CATCATTCTCCCTCT[C/G]CCTGCATCAGGGACA	78514
rs578718422	snp	C/G			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	GRCm38.p3	8:77516563	TTTTTTCCAGGGGTG[C/G]TGTCTACAAACAAAT	78514
rs578719362	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77508996	TCTTAATTTAATATA[C/T]ATATACACGTGTGTG	78514
rs578726042	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77489300	TGTGCGCGCGTGCAC[A/T]TGAGCGTGCATGTGT	78514
rs578747429	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77458004	TATCTATCTATCTAT[A/C]TATCTACCTACCTAC	78514
rs578752590	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77413685	TTTTGTGTGTGCATA[C/T]ATTTTGATGTCTCTA	78514
rs578753617	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77402537	ATGCACCTATAATTC[C/T]AGGAACTTGAGAGGC	78514
rs578759221	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77426772	AACTTTCAGCTGGGT[A/G]GTGGTGGCACACACC	78514
rs578762401	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77421897	CTGAGCAGCCAGAGC[G/T]GCTGGGCCCTCCACT	78514
rs578775971	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77447553	AAGACCCGCCAACAG[C/T]GCTCTGTGAAACAGC	78514
rs578836625	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77348027	TGTGTGTGTGTGTGT[A/G]CCTCATGCACATACC	78514
rs578840230	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77378853	TCCTCGTCATTGAGG[A/G]CGAGTGAGCTACCCC	78514
rs578849699	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77334421	AGGAGAGTGGAGCAG[C/T]GCGGAGAGAGAGAGA	78514
rs578853960	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77306047	ACAGGTAAATAGGTA[A/G]AAACCCTTAAAGAGG	78514
rs578857887	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77421073	CATCCACACACAGGC[A/G]CACACACACTACACA	78514
rs578860798	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77386689	ACCATCTATACAGCT[A/T]CAGTGTAATTACATA	78514
rs578887198	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77437524	CAAAGCGAAGTGGGT[A/G]GTTCCAGACCCTTGG	78514
rs578894605	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77368448	CCTGAAGCCATTCCA[C/T]CAACACCCTTACCTT	78514
rs578895329	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77299524	GCTCAAGTCTAAGTG[A/G]ATCAAAGAACTCCAC	78514
rs578896585	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77319911	CCTTCAAGAGGCTGA[A/C]AACGTCCTACCTCAG	78514
rs578899943	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77274184	TTGGTAAAATCAAAT[A/G]ATTGGTGTGTGTGTG	78514
rs578904374	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77307329	ACAAATGAAAGGGCA[C/G]CCACATTCATAAAAG	78514
rs578944138	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77447615	CCTACAGCTCCGCCC[A/G]TCTGCTCTCAACTGT	78514
rs578949524	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77451141	GCAGCTGACAGTGTG[C/T]ATCTTTCCGCACATT	78514
rs578952388	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77489279	GTGTGTGTGTGTGTG[C/T]GTGTGTGTGCGCGCG	78514
rs578953564	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77427013	GAAATTCATTTTAAC[C/G]CCAGTAAGTTTGGCC	78514
rs578956565	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77413910	TAAAAGAGCCATCTA[C/T]GGGGGGGGGGGGGGG	78514
rs578966301	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77505022	CATAGGGGCCAGCAG[C/T]CTAAAGGAAATTTCT	78514
rs578970498	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77480571	GTGCGCCACCACACC[C/T]GGCTCTTTTTTTTTT	78514
rs578972200	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77458023	CTACCTACCTACCTA[C/T]CTACCTACCTACCTA	78514
rs578989689	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77466781	AGACATTCATTCAGT[C/G]TCTCTCTCTCTCTCT	78514
rs579035404	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77261122	ACAGACAGACAGACA[A/C]AGAGCCCCTTTAACT	78514
rs579042189	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77449141	CACTGCCACATCCCT[A/G]GCCCTGTGCACACTG	78514
rs579046214	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77412394	ACCTTACCTTTTTTT[A/T]TTTGGAGATGGGGGA	78514
rs579063353	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77417891	CACGTGAGGGCACAC[A/G]CACACACACACCCAT	78514
rs579069697	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77485099	CTTCTACCAGTCACT[C/T]ACTTCTGTAAGGAAC	78514
rs579070147	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77445119	CAGCTTAAACAGATA[C/G]GGAGTTGGTAGCCAA	78514
rs579081984	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77461958	CAACAACCATTATAA[C/T]CACCACAATTTTTAC	78514
rs579094420	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77308288	TAGACAGATATCAAA[C/T]ACCAAAGTTAAATCA	78514
rs579095684	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77382049	CAAGCGTGCGCGCGC[A/G]CGCACACACACACAC	78514
rs579102367	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77296568	AAGACTGACTGGAAG[C/T]GTAGGGCCAAAGCAC	78514
rs579104859	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77456948	TCACAAAAGAACTCA[A/C]ATGATATGTACTCAC	78514
rs579106855	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77499012	GCCCGCTGCCCGCTG[C/T]CCGCTGCCTCTGCCT	78514
rs579113771	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77325519	CTTATACGACAGAAA[A/G]CTGCCCCTTGCCATA	78514
rs579122268	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77363454	GAGGAGGAGGAGGAG[G/T]AGGAGGAGGAGACAG	78514
rs579145532	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77306522	ATAAGAAGCCTACAG[A/T]ACTCTAAATAGATTG	78514
rs579197030	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77496964	TTTAATCCCAGCACT[C/T]GGGAGGCAGAGGAAG	78514
rs579199039	snp	A/G/T			upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77519526	GGGTGGGGGGGAGGG[A/G/T]GGGGTAGGTGGCATG	78514
rs579201729	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77278705	AACCATCTCAGAAAA[A/C]CAACAATTCCTCCCA	78514
rs579204412	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77489285	GTGTGTGTGTGTGTG[C/T]GTGCGCGCGTGCACA	78514
rs579228425	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77298203	CCTTTATAAGAGTTG[C/T]TGTGGTCATGGTGTC	78514
rs579234690	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77337838	CTCCCACCCTCTGGC[G/T]CCTTCTCTATGTGGG	78514
rs579237590	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77306753	TGCCAACACAGGCTA[A/C]TATACCCAGTAAAAC	78514
rs579254825	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77300058	GGAAGAAGGAAGAAG[A/G]AAGAAGAAGAAGAAG	78514
rs579256188	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77265731	GGACAGAGAGGGAAG[C/T]ATTGAACACCTCTTG	78514
rs579258040	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77308029	AACAAACAAACAAAC[A/C]AAAAAAAAACTATAC	78514
rs579293429	snp	C/G			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77485537	ACCAGACCAGACTTT[C/G]TCACCCAAAAAAAAC	78514
rs579297469	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77462225	GGCAGGGGTAGGAGG[A/G]GGAGGGAGGGAGGGA	78514
rs579311173	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77364229	CTTTTCCTGGGGTCC[A/G]TGGCTTGAAACGTGC	78514
rs579311174	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77433037	GGGGGAGCACGGAAC[C/T]TCGGAACTGGCCCCG	78514
rs579316621	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77449219	CACTGCCACATCCCT[A/G]GCCCTGTGCACACTG	78514
rs579321349	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77405972	AACTCTGAAAATGAC[G/T]TGCTGGCACAATACC	78514
rs579347834	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77411542	TACACATAGACACAT[A/G]CACACACATGTACAC	78514
rs579356175	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77388333	AAGCATTCAATACAC[C/T]TGTCAAAAAAAAAAA	78514
rs579367895	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77418623	CTTCATTGTTTTTAA[C/T]GTGGGGTTCTGTTCT	78514
rs579370294	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77443885	GAAAGAAAGAAAGAA[A/C]GAAAGAAAGGAAAAA	78514
rs579400921	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77305162	GTGGAACAACAATAT[A/G]AACTAATCAGTACCC	78514
rs579415573	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77268447	CAAGCAGCAAAAAAA[C/T]GCTACCCCATTTTTC	78514
rs579452477	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77283928	GAGGTTTGTAAGTGG[C/T]AAGACTGTGTGTGTG	78514
rs579467143	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77298778	TGACCCTAAAAATTC[C/T]ACCAGAGAACTCCTA	78514
rs579469395	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77308357	ACGAAGTAAAAGCAG[C/T]CATTAAAGTCTCCCA	78514
rs579479547	snp	A/G			utr-variant-3-prime	Arhgap10	GRCm38.p3	8:77250507	CCGGTGGGCAGGCCC[A/G]GGGAGGGGGTGGGGA	78514
rs579480980	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77306765	CTAATATACCCAGTA[A/G]AACTCTCAATTAACA	78514
rs579503995	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77474691	CCAAAGAAGTGAAGC[A/G]GGTAAAGCGCTTCGT	78514
rs579506004	snp	A/C/T			intron-variant	Arhgap10	GRCm38.p3	8:77495210	GGTTGGTAGAGTGTC[A/C/T]CTCTCTCTCTCTCTC	78514
rs579520456	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77457147	TGAAATGAAAGGATG[G/T]ACCATCTAGAGGCTG	78514
rs579521251	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77343414	AGAAGTGGGGCCATC[C/T]AGGACTCCTTGAAAG	78514
rs579523415	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77425695	AGGAAGAAGAAGAAG[A/C]AGAAGAAGAAGAAGA	78514
rs579531033	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77398603	TTCATTTTGTTTTTT[A/T]AAAGACTGTAGCTGA	78514
rs579536179	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77511822	ACAAAAAAAGAGTCG[A/C]ATACATAACCCTGAC	78514
rs579557949	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77433364	AGGAGGGACATGTGC[A/G]CGCATGTGTGTGTGT	78514
rs579565282	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77406407	GTGTGTGTGTGTGTT[A/G]CTAAATGTATCCCTA	78514
rs579616782	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77299893	GATTTCTGAGTTTGA[A/G]GCCAGCCTGGTCTAC	78514
rs579619966	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77380571	TATAAAATATTACCT[C/T]TTCTCGGAGTGCTGA	78514
rs579621287	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77414021	ATCTGAAAATAATCA[C/T]TCTTTCCAAGCTAAC	78514
rs579634523	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77445991	GTGTGTGTGTGTGTG[C/T]CTTTCTTCCAGGAAC	78514
rs579643814	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77320499	AAGTTCAGTTTCTTA[C/T]TCTTCTCTCCCCTAC	78514
rs579659909	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77351111	AAGTTCACCAGCTAC[A/C]GGCTTCATTTCATTC	78514
rs579664439	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77427046	GTTTTTGATCCTAAC[A/G]ACCCTAAGACCTTCC	78514
rs579671466	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77404754	CTCAACAGGAACCAT[A/G]CAGAAACCTTTTTTT	78514
rs579676742	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77513256	CTTCCCAGCGCAGTT[A/G]GAACTGAGTGAGAAG	78514
rs579679093	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77289676	AGGAGACTACACACT[G/T]CTCTTTCCATGCTCT	78514
rs579683451	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77275052	TGGGAGTGGGTGGGT[G/T]GAAGAGTGGGTGGGG	78514
rs579685860	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77306084	AAAAATCCCTTAAAA[A/G]ATTACATGAAAACAC	78514
rs579701665	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77254515	GAAGGGGGAAGGGAA[A/G]GGGAAAGGGGAAAGG	78514
rs579717888	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77495350	CTCTCTCTCTCTTTC[C/T]TTCTTTCTTTCCTTT	78514
rs579723207	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77475635	ACACACACACACTGT[A/G]AGACTTCATTGAGGA	78514
rs579733748	snp	C/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77369779	CGACTGTCCCACAGT[C/G/T]TGCTCTGCCACGTGC	78514
rs579736040	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77387207	TTATGTATCTGTGTG[A/T]GAGTGTGTGTGTGTG	78514
rs579738156	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77446974	GCCTGTGGCTGTCTC[C/T]CACTGCTTCTTCCAG	78514
rs579740101	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77425704	AAGAAGAAGAAGAAG[A/C]AGAAGAAGCAAACTC	78514
rs579743339	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77274911	CTAACCAGTACCTCC[C/T]AGAGCTCGTGTCTCT	78514
rs579746453	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77411419	GTACACACACACATG[C/T]ATACACATGTACACA	78514
rs579748844	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77307610	AAACAGACCTCCATA[A/G]ATACAAGAAGACTGA	78514
rs579755886	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77463846	ATTCACACCTCACAT[A/C]CATCCCTACCTCCAC	78514
rs579764467	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77457304	CACAGAAGTGGATGC[C/T]CACAGTCAGCTATTG	78514
rs579769971	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77433416	TCCCTTCTCTTGGCC[A/T]CACACACACACACAC	78514
rs579787458	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77299654	TGTGCTGTAAGATCA[A/G]GAATTGACAAATGGG	78514
rs579850580	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77415490	ACAATGGAGCCACTA[A/T]TGATATACTATAAAA	78514
rs579860927	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77307512	ACAGATATCTAGAGA[A/C]CATTTCATCCTAAAA	78514
rs579867005	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77481140	GATGGCCCACTGTCC[A/G]CACTGACTGTCTACA	78514
rs579875518	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77448708	ATCCCTAGCCCTGTG[C/T]ACACTGCCGCATCCC	78514
rs579901216	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77335979	ATTCTCTCTCTCTCT[C/T]TCTCTCACACACACA	78514
rs579917984	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77322256	ATGGAAGAGCCTGCA[A/G]AAATGAAGATGTCTT	78514
rs579920191	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77497004	TGAGTTCAAGGCCAC[C/T]CTGGTCTACAGAGTG	78514
rs579923510	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77356060	AGCACTACTGAAGAA[C/T]GCCTATATTATATAT	78514
rs579929719	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77380933	TGCAGACTGAAACTC[A/T]AAACATCTGGGGAGT	78514
rs579935576	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77290019	AGGGGATGAGACAGA[C/T]GTGGGAGGGGCTGGA	78514
rs579943416	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77306234	GAGTCACAGATGCAA[A/G]CATCACCAACAGAAT	78514
rs580003311	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77369543	TAAAAAAGTTAAAGT[A/G]TACAAACTATCGTTC	78514
rs580070470	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77469317	TCATTCTGGTAATGG[A/G]AGACACACACACACA	78514
rs580076779	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77511458	AGGAAAAAAAAGAAA[A/G]AGAGAAAGAAAGGAA	78514
rs580083958	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77452705	GAAGAGCCACACACC[A/C]GTCAGTCCAGTCATA	78514
rs580085753	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77356185	TATTAAAAAATGTAC[A/G]CAGGGGCTGCAGAGA	78514
rs580092025	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77422827	AGCCCTACTCTCCTC[A/G]TATCAACACCAGGCA	78514
rs580094838	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77307521	TAGAGACCATTTCAT[C/T]CTAAAACAAAAGGAT	78514
rs580095063	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77335990	CTCTTTCTCTCACAC[A/T]CACACACACACACAC	78514
rs580101553	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77411369	ACACACGCGCAAATA[C/T]ATACACGTGCACACA	78514
rs580109532	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77509573	ATTAAAAAAAGGGGG[A/G]GGATAAAGAATTTTG	78514
rs580113344	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77299721	ATACTGTCAATAAGA[A/C]AAAAAGGCCACCAAC	78514
rs580114800	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77274988	GAGAGGCCCATTGGT[C/T]GTGCAAACTTTATAT	78514
rs580115904	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77460184	GGGTTGGGGAGCACA[A/G]GTGGGCATGGCCGGG	78514
rs580117839	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77448737	CCTGGCCCTGTGCAC[A/T]CTGCCGCATCCCTGG	78514
rs580128901	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77443042	GGTTAATTTGTCTAG[C/G]CTTGGTTGTCCTAAA	78514
rs580138515	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77481166	CTACACATGAAATGA[C/T]CGTCTACTATTCACA	78514
rs580140350	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77497085	AAAAAAAAAAAAAAA[A/C]CAGTTCTGCCACAGA	78514
rs580163923	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77385264	ACACACACACACACA[C/T]ACACATACACTCACT	78514
rs580167340	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77416109	TAATCAGAATGTCTG[A/G]ATAAGGCTAAGGGGG	78514
rs580175107	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77404908	AGTGCTGGGATTAAA[A/G]GCGTGTGCCACCAAG	78514
rs580218371	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77298867	TGGCCTTTCTCTACA[C/T]AAAGGATAAACAGGA	78514
rs580245923	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77269135	ACAGGAGACAGAAAT[C/T]GGCTGTGCTCACATC	78514
rs580256584	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77306950	ATCCAAAAGAAGATA[G/T]CCACACAAACATAAA	78514
rs580279910	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77419386	GTCCCCTACCATCGG[A/G]ACAATGTTGAAGTGG	78514
rs580284269	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77406734	GGAGAAAAAGGTTCA[C/G]TGATAGTAAGATGAC	78514
rs580292836	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77510755	GCATGAGAGACAATG[A/C]CTTAATGTCCCTAAG	78514
rs580315808	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77283190	GGGAGGGGGAGGGGG[A/G]AGGGAGGAGGGAAGG	78514
rs580346056	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77300483	TGGAAATCAGTCTGG[C/T]GGTTCCTCAGAAAAC	78514
rs580374687	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77282402	AGAGGCCAAGGAAGA[A/G]TGCTGCTTATTGGCT	78514
rs580387960	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77407410	TTACTTTAAGTAGAT[A/G]GATAGATAGATAGAT	78514
rs580400219	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77493377	CCTCCTTCACTGGCC[C/T]ACAGGAACACAACAG	78514
rs580404012	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77464486	GAAGCTACGTTATTT[G/T]AGATTTAATCAAAAA	78514
rs580410177	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77434170	AGAGAACAAAGAACT[A/T]GTCATCCTAGAAAGA	78514
rs580414703	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77481092	ACATGAAATGGTGGC[C/T]CACTGTCCACGCTGA	78514
rs580414966	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77453800	GAGCTTCCCTTCCCA[C/G]ACACCCCTTCCTGCA	78514
rs580417198	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77443578	TGGCCTAGACACCAT[C/G]TTCAAAGAACACCTG	78514
rs580422999	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77458035	CTACCTACCTACCTA[C/T]CTACCTATCTATCTA	78514
rs580446167	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77385459	GAAGCAGAGGGAGCC[A/T]TCCAGATCTGCACCC	78514
rs580448538	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77308328	AAACCATCTAAACAG[C/T]CCCATAACCCCTAAC	78514
rs580449801	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77449761	TCCCCCTACTTCACA[A/G]AGTGATCTTGGGCAG	78514
rs580457948	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77473283	CCACACATTCACGCA[C/T]GGTTATTTTTTTTTT	78514
rs580478453	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77301180	TCTGGTTTGTAGTGT[C/T]TTTCCTGGCCGGTCG	78514
rs580535199	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77271708	ATTTCTTTAAAAAAA[C/T]TTTTTCTTCTGTGCA	78514
rs580537329	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77445481	AAATAAAGATGGGAG[A/G]AGAGACAGAGGCGGG	78514
rs580541585	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77425601	GAGGAGGAGGAGGAG[A/G]AGGAGAAGGAGAAGA	78514
rs580562933	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77457114	CATGGAAGGAGCTAC[G/T]GAGACAGAGTTTGGA	78514
rs580566989	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77307004	GCAACAATCACTATT[C/T]CTTAATATCTTTTAA	78514
rs580571435	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77373396	TGCTCATCTCAAACC[A/T]CAGCCTGGGCTAACG	78514
rs580577312	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77398585	ACTTAGCCTGGGGAA[G/T]TCTTCATTTTGTTTT	78514
rs580584988	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77412474	GGAACTCACTCTGTA[C/G]ACCAGGCTGGCCTGG	78514
rs580587814	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77450583	CTCAGAAAACCCCAT[C/T]CCCTCAAAGCACTAA	78514
rs580591982	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77299013	CTGAAGAAAGAAATT[A/G]AAGAAGATCTCAGAA	78514
rs580596060	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77341898	TCTCAGGAAAAAAAA[A/T]AAAAATAAAAAATAC	78514
rs580601976	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77486711	AACATCTGATAGACA[A/G]AAGGGCCCCCCTCCC	78514
rs580607531	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77487540	GTAGGCACCCTTCAC[C/T]GCAGACGCCTCACCA	78514
rs580611506	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77401945	CCTCCTCCTCCTCCC[C/T]CTCCCCCTCCTCCTC	78514
rs580664861	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77375072	CACACGTGGCCAGGA[A/G]CGTCTAAGTATAAAG	78514
rs580667112	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77503970	TCGGAACCCTCATGA[A/G]CCCCCCCCCCCTCCA	78514
rs580675397	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77447428	AGACCACATTTCAAT[C/G]TCTTCCTCTCATCAG	78514
rs580679811	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77464950	TTTTTTAAAAAAAGT[A/G]CCTTACCTAGAAAAC	78514
rs580690416	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77315398	AGACTTCATAATGGG[G/T]GCTGACAAACACCAG	78514
rs580707009	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77299183	CTGCAAATTCATCTG[A/G]AATAACAAAAATACT	78514
rs580713082	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77457879	AAAAACAGCAAGAGC[A/G]CACATGCATGATACA	78514
rs580734231	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77324182	GGGAAGGGCTGGAGA[A/G]TCTGTTCATCTTTGC	78514
rs580758803	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77434985	TGTGAAGGGGTCAGG[A/G]GGAGCAGATTCCAGC	78514
rs580789743	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77386615	CTGAGAGAGCAGGGC[G/T]GACCAGAGTGAGCAG	78514
rs580803129	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77252979	GCCTATCTAAGTTCA[C/T]ACCACATTTTGTCAG	78514
rs580805217	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77407422	GATAGATAGATAGAT[A/G]GATAGAGATGGATGG	78514
rs580806894	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77307019	CCTTAATATCTTTTA[A/T]TATCAATGGACTCTA	78514
rs580819593	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77305369	TTTGGGATAGCATTT[C/G]AAATGTAAATGAAGA	78514
rs580821344	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77287434	CTCTCAAATGTTACC[C/T]ATGACATATAGAGGG	78514
rs580821545	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77496585	AGCTGAACACACCCA[A/T]AGACAAATTGCCTTA	78514
rs580844240	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77412719	TGTTTGTAGTGCAGG[C/G]GCTTTACCAGCTAAG	78514
rs580863595	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77386636	GAGTGAGCAGAGGTC[C/T]TAAAATTCAATTCCC	78514
rs580896699	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77306383	ATATAATGAGAAGAC[A/C]AAACCTAAGAATAAT	78514
rs580902116	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77408091	TTAAAAAAAAATTAA[C/T]CCTTTATACATAAAG	78514
rs580916482	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77261072	AGAGAGAGAGAGAGA[C/G]AGACAGAGAGAGAGA	78514
rs580922386	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	GRCm38.p3	8:77516584	ACAAACAAATGGAAT[A/G]AACGCCCAGAGATGG	78514
rs580927216	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77368249	CTGCACCAGCCTTTT[C/T]TTCCAAAATTCTTTC	78514
rs580967768	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77489252	TTCTCCCTCTCTCTC[G/T]CTGGTGTGTGTGTGT	78514
rs580969222	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77400260	GCTCCTAGTTTTATG[C/T]TACCAGATTTTAATT	78514
rs580970946	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77370492	TCAGGGTCTGTTGGC[A/T]GATTTCCCAGCCTGC	78514
rs580980945	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77411464	CACACATGTATACAC[A/G]TGCACACACACGTGC	78514
rs580983617	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77465837	TATGGCTTCAACAAT[C/T]AAATATAAAGTTGGA	78514
rs580985927	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77451119	ATCCCTCCCCTTCCC[A/G]CCTCCTGCAGCTGAC	78514
rs580993349	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77307648	CCATGTATCCTATGA[A/G]ATCACCGCAGACTAA	78514
rs581002479	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77504687	TGGCACACTGGCCAG[C/G]ATGGTCACAGTGCGA	78514
rs581017238	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77276170	GCACACACCAATGCA[C/T]ACACACACACACACA	78514
rs581030322	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77436551	TTAGTTAGTAACTAC[C/T]GTTTAACGGATCAGC	78514
rs581036302	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77421037	ACACCACCTGCACAC[A/C]CACACACACACACGC	78514
rs581046660	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77300015	AAAGAAGAAGAAGAT[A/G]GAAGATGGAAGATGG	78514
rs581058512	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77261084	AGAGAGACAGAGAGA[C/G]AGAGAGAGAGACAGA	78514
rs581085439	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77461560	GCCGTGCTGACTGCC[A/C]TCTTCCTTCACTCCC	78514
rs581095229	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77260768	AAGGTCCATCAGGGC[A/G]GGAACTCAAGCTGCT	78514
rs581103525	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77306303	CATAGAAAACATTGA[C/T]ACAACAGTCAAAGAA	78514
rs581120766	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77382035	TGTGTACATAAGCTC[A/G]AGCGTGCGCGCGCAC	78514
rs581128456	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77449127	CCTAGCCCTGTGCAC[A/T]CTGCCACATCCCTGG	78514
rs581137444	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77405338	TCCATCACACTCATA[A/C]CCAAACCGCTGGGCT	78514
rs581139534	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77306465	CAATAAAATTATAGA[A/G]GAAAACTTCTCTAAC	78514
rs581141508	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77325232	CAAGGAGTCAGGAGG[A/C]TAGCACAAATTAGCT	78514
rs581147223	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77362295	AAGCCTTGGGGAATC[A/G]CTACAAACTTTTACA	78514
rs581157878	snp	C/G			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77485084	AGCTCTTCCCCTCAG[C/G]TTCTACCAGTCACTC	78514
rs581161164	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77296053	AGGTATGTCACTGTG[A/G]GTGTGGCTTTAAGAC	78514
rs581185955	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77455326	GGTACCCCCTTGTCA[A/G]TGATCAAGAAATGAG	78514
rs581230107	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77432372	TAGCAATAGTCTCAT[C/T]CCAGGTTCCAGGGCT	78514
rs581237148	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77443770	CGGATTTCTGAGTTC[C/G]AGGTCAGCCTGGTCT	78514
rs581248435	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77411533	ACACACGTGTACACA[C/T]AGACACATGCACACA	78514
rs581254191	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77472135	TTATATATACATATA[C/T]ATATATACACACACA	78514
rs581273524	snp	C/T			intron-variant, utr-variant-5-prime	Arhgap10	GRCm38.p3	8:77492842	CACTAGCTCACTCTC[C/T]ACACTTCTGCACCCA	78514
rs581294607	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77459946	GATGACAAGTGACAA[C/G]TGCACGTGTTAGTTT	78514
rs581304172	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77299457	GCTAGCACAACTGGC[A/G]GTTATCATGTAGAAG	78514
rs581324978	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77337433	CGTCTAGCCCATACA[C/G]CCCTGCGCTAACCTC	78514
rs581332540	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77371425	GCATAGAGGAAAGTA[A/G]CACTACAGACAAGAG	78514
rs581355087	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77300042	ATGGAAGATGGAAGA[A/T]GGAAGAAGGAAGAAG	78514
rs581357309	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77308012	GAAGTCAACCAAGTA[A/G]AAACAAACAAACAAA	78514
rs581359760	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77511476	AGAAAGAAAGGAAGA[A/G]AGAGAGAGAGAGAGA	78514
rs581367644	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77449167	CACTGCCGCATCCCT[A/G]GCCCTGTGCACACTG	78514
rs581385448	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77511488	AGAAAGAGAGAGAGA[A/G]AGAGAGAGAGAGAGA	78514
rs581387283	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77307224	AATATTGACCAAAAT[C/G]GAATTTCAACCTAAA	78514
rs581401641	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77417039	TATCACAGTAACGAG[C/T]ACAGGGAAAGGAGTC	78514
rs581406854	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77273433	TTAAAAAAAACACAA[A/C]AAAACAAACCCAGCA	78514
rs581421038	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77381982	AAAAAAAGGGGGGGG[C/G]CTTTAAGGAGGTGGT	78514
rs581424941	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77448816	CTAGCCCTGTGCACA[C/T]TGCCGCATCCCTGGC	78514
rs581439040	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77344815	CTAATATTGATTTAG[A/G]AAGAAAAAAAAAGTC	78514
rs581448004	snp	A/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77443894	AAAGAAAGAAAGAAA[A/G/T]GAAAAAAGTTATAGT	78514
rs581449430	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77284830	CCTCCCCTTGATTTT[A/G]TAGGTAATGGGACAC	78514
rs581462423	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77305276	AAACTTTATATGCCC[C/T]AATACAGGGGAAAGC	78514
rs581465311	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77462184	AAGTTCTAGGCTAGC[A/C]AGGGATAGACAGACC	78514
rs581481347	snp	C/T			intron-variant, utr-variant-5-prime	Arhgap10	GRCm38.p3	8:77493093	AAGTTGCCAAGGCAA[C/T]TCAGAGAAACCCTGA	78514
rs581498241	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77404918	TTAAAGGCGTGTGCC[A/T]CCAAGCCTGGCTGCA	78514
rs581513861	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77472153	ATATACACACACATA[C/T]ATATATATATACACA	78514
rs581516058	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77483329	GGAGGGGGAGGCGGA[C/G]GGGGAGGGGGAGGGG	78514
rs581523007	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77443893	GAAAGAAAGAAAGAA[A/G]GGAAAAAAGTTATAG	78514
rs581523285	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77311319	TTTTTTTTACACATT[A/G]AAAAATAGCCTGCGC	78514
rs581542076	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77286191	CAGTGACAGGCTCCA[C/G]TCAGACGCCATCATG	78514
rs581545731	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77388370	ACCCACTTGTGTAAA[A/G]TAGGAGAAGTTGAGA	78514
rs581564753	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77424956	TGTGTGAGTGTGTGT[A/G]TGTTCTCAACGATAA	78514
rs581567422	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77337848	CTGGCTCCTTCTCTA[C/T]GTGGGTATGCTAGGT	78514
rs581571504	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77411550	GACACATGCACACAC[A/G]TGTACACACACAGAC	78514
rs581608357	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77438181	CATTCCCACACCTTG[C/T]AAGAACTGATTGCCA	78514
rs581628763	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77345609	TCCTTCGAACACCCT[C/T]TCTCTCTCCTTGCAA	78514
rs581631194	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77466828	CTCTCTCTCTCTCTC[C/T]CCTCCCTTTGCTTGA	78514
rs581641500	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77496162	ATAACGAATGCCACG[A/G]CATGTTATTTTCAAA	78514
rs581652201	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77305289	CCCAATACAGGGGAA[A/C]GCCAGGACCAAGAAG	78514
rs581717044	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77421210	ACTACACAGCAAGAT[C/T]GTGGCTTTAAAAAAA	78514
rs581730117	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77404804	GTTTTCTGAGACAGG[A/G]ATTCTCTGTATAGCC	78514
rs581733573	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77514703	CACAGTTTAATTGGT[G/T]TTTGTTTGTTTGTTT	78514
rs581735624	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77489281	GTGTGTGTGTGTGTG[C/T]GTGTGTGCGCGCGTG	78514
rs581746107	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77451333	AGAGAGGGGGAGGGA[C/G]GGAAGGCGGGAAATC	78514
rs581750500	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77274863	AAGGAGCTGGGGGGA[C/T]CTGCAACCCTATAGG	78514
rs581762749	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77307371	AAGCTCAAAGCACAC[A/G]TTGCACCTCACACAA	78514
rs581778644	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77457541	CAGTACAGGGGAACG[C/T]CAGGGCCAAGAGGTG	78514
rs581783978	snp	A/C/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77447071	AAGGGGGGGAGGGTT[A/C/G/T]GAGTGGTTGATTTTT	78514
rs581795200	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77505370	ATGCTCCCCTAGAGA[A/G]CTAAGAGTTCTGACC	78514
rs581832911	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77380576	AATATTACCTTTTCT[C/T]GGAGTGCTGATGGCT	78514
rs581843871	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77458055	CTATCTATCTATCTA[C/T]CTATCTATCTATGCC	78514
rs581845538	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77489287	GTGTGTGTGTGTGTG[C/T]GCGCGCGTGCACATG	78514
rs581860181	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77300131	GAAGAAGAAGAAAGA[A/T]GAAGAAGAAAGATGA	78514
rs581874614	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77299591	GTGGGGAAAAGCCTC[A/G]AAGATATGGGCACAG	78514
rs581885462	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77387058	AAGGAAGGAAGGAAG[A/G]AAGAAAGAAAGAAAG	78514
rs581909831	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77421586	AAGTGTAGTATTTGT[C/T]TGGTACTTTTAATTG	78514
rs581911799	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77335424	GACACCCCGTCTCCC[C/T]GGCCTTCCCATTCTG	78514
rs581915755	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77410329	AATTCACCTAAGCAA[A/T]ATGTCACCCAGCAAG	78514
rs581917722	snp	A/C/T			intron-variant	Arhgap10	GRCm38.p3	8:77369238	GGGATTAAAGGTGTG[A/C/T]GCCACCACACCCGGT	78514
rs581930226	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77447554	AGACCCGCCAACAGT[A/G]CTCTGTGAAACAGCC	78514
rs581932371	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77467962	CTATAGACAGTGACA[C/T]AGACACATGGTAGCC	78514
rs581943434	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77414757	TACTCATTTGTATTT[A/G]TTTATTTGTTTGTTT	78514
rs581963539	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77480522	AACTCAGAAATCCAC[C/T]TGCCTCTGCCTCCCG	78514
rs581964160	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77448169	GTTGTGCGCATGCGC[A/G]CGCGCACACACACAC	78514
rs581968387	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77278771	AGCTAGCTGTTGGAA[C/T]GTAAGTCTTGAAAAG	78514
rs581975923	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77335986	CTCTCTCTTTCTCTC[A/T]CACACACACACACAC	78514
rs581991854	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77299659	TGTAAGATCAGGAAT[C/T]GACAAATGGGACCTC	78514
rs582008206	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77452145	CAAAAAACAAAAAAA[C/T]GTACTATGTAGCCAA	78514
rs582008537	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77496988	GAGGAAGGCAGATTT[A/C]TGAGTTCAAGGCCAC	78514
rs582044861	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77267210	AGGCAAAGAAGGGGA[A/G]AGAGCACAGAAAGCA	78514
rs582046630	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77458015	CTATCTATCTACCTA[C/T]CTACCTACCTACCTA	78514
rs582050745	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77410649	TTATGAAACCTCTGC[A/G]TGCCTAACTGAATGA	78514
rs582051707	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77481100	TGGTGGCCCACTGTC[C/T]ACGCTGACTGTCTAC	78514
rs582054797	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77426908	TGTCTTGTGGGAAAG[C/T]GGTGGCAGGGTGGTG	78514
rs582063338	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77496597	CCAAAGACAAATTGC[C/G]TTATTTTTTAAAAAA	78514
rs582075981	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77308227	TCCTACTATAAAAGC[C/T]TATATTCAACAAAAC	78514
rs582082583	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77372329	CATGGTCTGATTCTT[A/G]ACAAAAGGAATGAGC	78514
rs582083293	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77307513	CAGATATCTAGAGAC[C/T]ATTTCATCCTAAAAC	78514
rs582096169	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77369279	AATTATGTATTGCAC[A/G]TTCCCTTTCAACTTA	78514
rs582131840	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77468705	GTTGAGAATCTGCCC[A/T]GCTGAGCCTAAGGCT	78514
rs582131997	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77452594	CCCCAGACGTGGTGG[C/T]ACGTGCCTGTATCCC	78514
rs582138399	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77441549	TGAAAAGTATTATTA[C/T]GCTTTATTATATGTG	78514
rs582145236	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77463744	ATGCCAACAAGCAAT[A/G]CCAGGTGAATAGTGT	78514
rs582169264	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77502864	GTCTTCTACAGAGAG[A/G]AGCATCACCTATATG	78514
rs582175368	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77411613	ACACACACACACATA[C/T]ACACATACACACCAA	78514
rs582179856	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77377804	ATGTCTCAGGATAAG[C/T]ACACACACACAGACA	78514
rs582195050	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77306009	AGGGCATAAATAACT[C/T]CCTTAAAGAAATACA	78514
rs582195502	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77274919	TACCTCCCAGAGCTC[A/G]TGTCTCTAGCTGCAT	78514
rs582196105	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77444164	AGGATGCTCAGAAAC[G/T]GAATCCTCACAGGCT	78514
rs582204952	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77318701	AGTCCCTCGTCAGTT[A/G]GGAACGCTCTGTCCC	78514
rs582210439	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77338831	TGCTTTCTGTTGCTG[G/T]GACCAAACTGACCAA	78514
rs582213070	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77347416	GTTGTTGTTGTTGTT[G/T]TTTCGAGGCAGGGTT	78514
rs582215683	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77289677	GGAGACTACACACTG[C/T]TCTTTCCATGCTCTT	78514
rs582221885	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77509479	GAAATAGAGGAGGGG[C/G]TGGAAGAGAAGGAAG	78514
rs582228582	snp	C/T			intron-variant, downstream-variant-500B	Arhgap10	GRCm38.p3	8:77358182	CCACTACGCCCTAGT[C/T]CCCCCATCTCCCTCT	78514
rs582231366	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77300326	CAGGGAAATGCAAAT[A/C]AAAACAACCTTGTGA	78514
rs582239988	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77489301	GTGCGCGCGTGCACA[C/T]GAGCGTGCATGTGTG	78514
rs582258207	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77485370	GGACCACGAGAAACA[A/G]GCTGGGGGGCTAGCA	78514
rs582275829	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77306841	AATATCTTTCCACAA[A/G]TCCAGTCCTACAAAG	78514
rs582295616	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77363460	GAGGAGGAGGAGGAG[A/G]AGGAGACAGTGTCTC	78514
rs582336008	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77511500	AGAGAGAGAGAGAGA[A/G]AGAAAAGAAGAAAGG	78514
rs582338854	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77261648	AAAACTTCTATCTGG[A/C]CACTTGGAAAGTCCA	78514
rs582344359	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77449367	CCTGTGCACACTGCC[A/G]CATCCCTGGCCCTGT	78514
rs582347261	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77472160	CACACATATATATAT[A/G]TATACACATATATAC	78514
rs582349204	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77493255	GAGAAGAAGGAAGAG[A/G]AAGAGGAGGAGGAGG	78514
rs582385267	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77456953	AAAGAACTCACATGA[A/T]ATGTACTCACTGATA	78514
rs582392447	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77433365	GGAGGGACATGTGCA[C/T]GCATGTGTGTGTGTG	78514
rs582396408	snp	A/C/G			intron-variant	Arhgap10	GRCm38.p3	8:77425570	GGAGGAGGAGGAGGA[A/C/G]GAGGAGGAGGAGGAG	78514
rs582400304	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77456925	TCATCCTGAGTGAGG[A/T]AACTCAATCACAAAA	78514
rs582401750	snp	A/C			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77493375	TTCCTCCTTCACTGG[A/C]CTACAGGAACACAAC	78514
rs582406611	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77406663	AGCCATCTGAGAGAG[A/G]CATCAATGGCTTTCT	78514
rs582418854	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77253613	GAAAGTGCAACACAG[A/G]CCCCATGCAAAATGT	78514
rs582466002	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77296569	AGACTGACTGGAAGC[A/G]TAGGGCCAAAGCACA	78514
rs582475831	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77325798	GCCCATCACATGCAA[C/T]CCTTATTCTGAGGAC	78514
rs582496486	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77405580	GCCCCAGCTCACTAG[A/T]GTTTGCGTCACAGGA	78514
rs582515386	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77300691	AGTACATTTACACAA[C/T]GGAGTTACTACTCAG	78514
rs582517053	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77412398	TACCTTTTTTTTTTT[G/T]GAGATGGGGGAGGAG	78514
rs582517410	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77308294	GATATCAAATACCAA[A/G]GTTAAATCAGGATCA	78514
rs582517790	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77485823	AGTTGGGAAAAGCAG[A/G]TGCCAAGCACTATGA	78514
rs582525747	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77449257	CCTGGCCCTGTGCAC[A/T]CTGCCACATCCCTGG	78514
rs582535561	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77445246	AAGGAAGGAAGGAAG[A/G]GAGAGAGAGAAAGAA	78514
rs582554914	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77511519	AAAGAAGAAAGGCAG[A/G]CAGGCTACGAAGCTG	78514
rs582556807	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77472587	TTAAAAGATATATGT[A/G]TATATAATATAACAA	78514
rs582604354	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77511512	AGAGAGAAAAGAAGA[A/C]AGGCAGGCAGGCTAC	78514
rs582641673	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77433038	GGGGAGCACGGAACC[A/T]CGGAACTGGCCCCGC	78514
rs582642349	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77319929	CGTCCTACCTCAGGC[A/T]CAGGTATTATGGAGC	78514
rs582653188	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77287923	AAAGAGAAAAAAAAG[A/G]GAAAGAGAAAGAGAA	78514
rs582670833	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77463024	ATGTAACACAAGAGA[A/G]AGGTGAGGAGTCTGC	78514
rs582700219	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77308037	AACAAACAAAAAAAA[A/C]ACTATACAAAGAATC	78514
rs582726662	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77509602	TGAATGGAGGTTTAT[A/G]CCTTACCTTAAACCA	78514
rs582744471	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77445662	AGACAGAGACAGAGA[A/C]AGAGACAGAGACAGA	78514
rs582747857	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77327669	GTAAGGCAAATTTGT[A/T]TGTGCATTTTTTTCT	78514
rs582766334	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77298204	CTTTATAAGAGTTGC[G/T]GTGGTCATGGTGTCT	78514
rs582774841	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77306755	CCAACACAGGCTAAT[A/G]TACCCAGTAAAACTC	78514
rs582797890	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77386995	AGAAAGAAAGAAAGA[A/G]AGAAAGAAAGAAAGA	78514
rs582815156	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77503990	CCCCCCCTCCAGCAA[C/T]TGTTAAATGACTGTA	78514
rs582817859	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77254503	TTTAAAAAGAAGGAA[A/G]GGGGAAGGGAAGGGG	78514
rs582837786	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77493696	ATGTTGGAAAGCTAT[C/T]TGTTACTGCAACAGA	78514
rs582845884	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77474392	TCATGTAGGGGGAAA[C/T]TTTTTTAAGTTGGAA	78514
rs582847574	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77457128	CGGAGACAGAGTTTG[A/G]AGCTGAAATGAAAGG	78514
rs582857216	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77385123	GAGTCATCCAATGAC[C/T]GCCTGGGGTAGAAGT	78514
rs582857711	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77334422	GGAGAGTGGAGCAGC[A/G]CGGAGAGAGAGAGAA	78514
rs582858242	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77307622	ATAAATACAAGAAGA[C/T]TGAAATAATCCCATG	78514
rs582873365	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77275211	TGTGTGTCCGTGCCT[C/G]TGTGTGTGTGTGTGT	78514
rs582874271	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77299556	TAAAACTAGAGACAC[A/G]GAAATTTATAGAGGA	78514
rs582876248	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77274234	GTGTGTGTGTGTGTG[A/T]AAGAGAGGGAGAAGG	78514
rs582891101	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77307345	CCACATTCATAAAAG[C/T]AACTTTAAGAAAGCT	78514
rs582916123	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77491338	AAAAAACACCTTGCT[A/G]TGGAAGCTGCAGTGG	78514
rs582918498	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77460974	TCACAAAATAACCTG[A/G]CCTACAACACAACAA	78514
rs582947456	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77496939	GGGCTGGGCAGTGGT[A/G]GCGCATGCCTTTAAT	78514
rs582959466	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77458027	CTACCTACCTACCTA[C/T]CTACCTACCTACCTA	78514
rs582968198	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77488031	ACCCTCAGAAGGTGG[C/T]TGACTGTGACAGCTG	78514
rs583004550	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77427014	AAATTCATTTTAACG[C/T]CAGTAAGTTTGGCCA	78514
rs583006967	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77413934	GGGGGGGGGGGGGTG[G/T]TATAAAAGGTGTTCG	78514
rs583014854	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77299928	TGAGTTCCAGGACAG[C/T]GAGGACTATACAGAG	78514
rs583020906	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77336177	CTCTGGTCCTAAGCA[C/T]TCTGAGAAAGAGCTG	78514
rs583058298	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77512447	TTCCAGGTGAGACCT[C/T]GACTGCGGGGGAGGG	78514
rs583062299	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77465043	TGCCGAGTGCTGAGG[C/T]CTACAGGTTCCTACC	78514
rs583095369	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77257734	TACTTGTGAGCACTT[C/G]AGCTGTTGTGCATTT	78514
rs583112383	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77511084	GTATGAAAAGCTAGA[A/G]GACCGGTCTGTAAGC	78514
rs583113618	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77306107	GAAAACACAACCAAA[C/G]AGGTAAAGGAATTGA	78514
rs583133151	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77255303	AAGCCCTGGGTGTTC[A/C]AGCCAACATGCTAGA	78514
rs583164861	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77470206	GCATACTCAAGAGGG[G/T]CTTGATAACCCCATT	78514
rs583167631	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77481148	ACTGTCCACACTGAC[C/T]GTCTACACATGAAAT	78514
rs583171670	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77423869	GCAATGCATGGCACA[A/C]AGAGTCCTGGGCAGG	78514
rs583177787	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77448711	CCTAGCCCTGTGCAC[A/T]CTGCCGCATCCCTGG	78514
rs583186420	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77411421	ACACACACACATGCA[C/T]ACACATGTACACATG	78514
rs583206929	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77370099	AGTGAATTCACAATC[C/T]TGAGGGGGGGGGGGG	78514
rs583207014	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77453804	TTCCCTTCCCAGACA[C/T]CCCTTCCTGCAGGAG	78514
rs583210205	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77298825	TCAGCGCAGTAGCTG[G/T]ATATAAAATTAACTC	78514
rs583213020	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77443579	GGCCTAGACACCATG[C/T]TCAAAGAACACCTGC	78514
rs583213315	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77387209	ATGTATCTGTGTGAG[A/T]GTGTGTGTGTGTGTG	78514
rs583215139	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77423401	CTGGGCAGGAGAGGT[A/G]GGTTCCGGGGGTTGG	78514
rs583239508	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77370774	GTCTTTCCTATAATC[A/G]GCCTCACTTCCCCTC	78514
rs583268456	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77290202	TGTATTATAATCAAG[C/T]CCATAACAAAACAAA	78514
rs583309273	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77404902	CTCCTGAGTGCTGGG[A/G]TTAAAGGCGTGTGCC	78514
rs583314046	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77374528	ATCCCCTTCCTTTTA[C/T]AGGGAAGAAAGGGTT	78514
rs583327195	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77323107	ATGACACTTAACTCA[A/T]GAGCGAGAAAATGTG	78514
rs583327365	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77430463	TAAGGAATGAAGCAG[A/G]CCTCGAAGTAAACTC	78514
rs583331134	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77356061	GCACTACTGAAGAAC[A/G]CCTATATTATATATA	78514
rs583331419	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77415888	GCAAATAAAATAATA[A/G]ATTAAATTGTGACAG	78514
rs583341324	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77309437	GCTGAGCCTGGCCTT[A/T]CTGGCCTGTAACCCG	78514
rs583342330	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77460015	GGAGAAGAGCAAGAC[A/G]GCTAGGCAATGGAGC	78514
rs583355380	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77411478	CGTGCACACACACGT[A/G]CACACACATGCACGC	78514
rs583368643	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77306260	AGAATACAAGAGATA[C/G]AAGAGAGAATCTCAG	78514
rs583376149	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77497015	CCACTCTGGTCTACA[A/G]AGTGAGTTCCAGGAC	78514
rs583377204	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77511460	GAAAAAAAAGAAAAA[A/G]AGAAAGAAAGGAAGA	78514
rs583411727	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77306951	TCCAAAAGAAGATAG[C/T]CACACAAACATAAAA	78514
rs583419784	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77404581	AGCTCTTAACTGCTA[C/T]TTTAGACCAAATGTT	78514
rs583423808	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77471394	TTATCCAAGGAGCTA[A/T]AGGGATCTGCAACCC	78514
rs583426234	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77269144	AGAAATTGGCTGTGC[C/T]CACATCCCTGACCAG	78514
rs583436129	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77454842	CAATTGCCAAGAAAT[A/C]CTTACAGCAACCCCC	78514
rs583457521	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77425698	AAGAAGAAGAAGAAG[A/C]AGAAGAAGAAGAAGC	78514
rs583477426	snp	A/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77457261	TGATATAGCTGTCTC[A/G/T]TGTGAGACTATGCCG	78514
rs583487700	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77457437	ACCCCCCCAGAGCTC[A/G]TGTCTCTAGCTGCAT	78514
rs583490945	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77344282	ATTTGCTTTTTTATT[C/T]CTCTGAGCTAAAAAG	78514
rs583500593	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77495556	ATGTGAGGCCTCCAT[C/G]CTAAGAAAATGTAGC	78514
rs583504414	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77399263	CAAAGAAATCATCTT[A/G]TGGTTGGGAGTCACC	78514
rs583519146	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77407332	CTCCATTTACTTTAG[A/G]TAGATAGATAGATAG	78514
rs583532362	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77474823	CTGAGGTCATGGGTC[A/G]CAGGTCAAAGGTCAC	78514
rs583533890	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77450593	CCCATCCCCTCAAAG[C/T]ACTAAATGCATCAAA	78514
rs583535987	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77436518	ACAGAAAGGATGTCC[G/T]ATGGCAACGTTAGTG	78514
rs583535996	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77495276	TCCCTCCCTTCTCTC[C/T]CTCTCCCCCCTCCCT	78514
rs583567507	snp	A/T			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77485261	CTGTCTGCTGAACGG[A/T]CTGACCCTACCCCAG	78514
rs583596196	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77305220	GTAGCAGAAGATGGC[C/T]TAGTCAGCCATCATT	78514
rs583598447	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77283935	GTAAGTGGCAAGACT[C/G]TGTGTGTGTGTGTGT	78514
rs583600881	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77329197	TTCCCTTCCATGCTA[A/C]GCTGAGCATGACCCT	78514
rs583631634	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77298884	AAGGATAAACAGGAT[A/G]AGAAAGAAATTAGGC	78514
rs583657131	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77481169	CACATGAAATGACCG[C/T]CTACTATTCACACTG	78514
rs583662120	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77497120	CTATTTTTCATGAGT[G/T]TGATTTTTTTTATAT	78514
rs583663569	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77304806	ATCAAGAAGGAATAC[A/C]AACACGTGGATACTT	78514
rs583671579	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77341901	CAGGAAAAAAAATAA[A/C]AATAAAAAATACGAA	78514
rs583675526	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77475919	AGACACTGGCCAGTG[A/T]CATCACATTGAAGGG	78514
rs583681837	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77447004	GCAGCTACCCCTCTT[C/G]TCAAATATCACTTTT	78514
rs583682959	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77285246	ATATATACGCGTGTG[C/T]GTGCGTGCGTGCGTG	78514
rs583686600	snp	C/T			downstream-variant-500B	Arhgap10	GRCm38.p3	8:77249922	CATAAGACTGGGCCA[C/T]GCCTGGGCCTGGAGT	78514
rs583686832	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77514663	ATGTGCTCAAGTGCT[C/G]ACCTGGCTCTCGCTC	78514
rs583694780	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77305278	ACTTTATATGCCCCA[A/G]TACAGGGGAAAGCCA	78514
rs583721934	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77385273	CACACATACACATAC[A/T]CTCACTTTACAACCC	78514
rs583754481	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77487356	ACGCACGCACACACA[C/G]ATACACACTAGCTGG	78514
rs583767028	snp	A/C			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77503497	CCCTTCAGTAAGTCA[A/C]ATGTAATAAGCCATT	78514
rs583804826	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77400537	TTGCCTGTGTGTATG[C/T]AGTACATTATATATG	78514
rs583823884	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77464078	TGGATCCCATAAGGA[A/G]TCTATTCTTAGAAAA	78514
rs583824009	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77425707	AAGAAGAAGAAGAAG[A/C]AGAAGCAAACTCAGC	78514
rs583826089	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77345011	TGTCCCCTTCCCTGC[C/T]CTCCAGTCTTCCTTC	78514
rs583827941	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77449438	CCCTAGCCTTCTTAC[A/G]TGGGTTGGGGGAAGC	78514
rs583832241	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77412725	TAGTGCAGGCGCTTT[A/C]CCAGCTAAGCAGCTT	78514
rs583834060	snp	A/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77374755	GCTCACATGCAGACA[A/G/T]TTGTCCCTACTGCAA	78514
rs583836353	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77407414	TTTAAGTAGATAGAT[A/G]GATAGATAGATAGAG	78514
rs583839420	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77443163	ACAGCTTTTAAAACA[A/C]AGTAAGAGAGTCATA	78514
rs583845676	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77381743	ATGTATGTGGCTAAA[A/G]GTCAGACACAGGGCT	78514
rs583855367	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77469358	CACACACACACACAC[A/C]CCCCTCGCATGCTGG	78514
rs583857089	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77308350	ACCCCTAACGAAGTA[A/G]AAGCAGCCATTAAAG	78514
rs583872125	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77323954	CTGAAACATGAGGGC[C/T]CATTGCTTACTGTAG	78514
rs583877808	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77283204	GGAGGGAGGAGGGAA[G/T]GGAAGATGTAACTTA	78514
rs583884943	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77411379	AAATACATACACGTG[C/T]ACACACAGACACACG	78514
rs583894647	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77292003	AATCTTGGTTTTTTT[A/C]AAAGAAGATAATAAA	78514
rs583906326	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77373479	ACGCACCACAGACCT[A/G]GGCTTGGGAGGTTGG	78514
rs583910330	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77307011	TCACTATTCCTTAAT[A/G]TCTTTTAATATCAAT	78514
rs583912108	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77425686	GAAGGAAGAAGGAAG[A/C]AGAAGAAGAAGAAGA	78514
rs583914496	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77398596	GGAAGTCTTCATTTT[G/T]TTTTTTAAAAGACTG	78514
rs583915703	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77329941	AAAAAAACCATGTTT[G/T]TGAGCTGCTGACAGT	78514
rs583918870	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77412480	CACTCTGTAGACCAG[A/G]CTGGCCTGGAACTCA	78514
rs583931058	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77299105	GCCAAAAGCAAACTA[C/T]AGATTCAATGCAATC	78514
rs583944069	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77503736	AAGCTGGAGCACAAA[C/T]GGTGCAAAGCTTCTT	78514
rs583944774	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77447537	GCCCCACTCTGTGGG[A/G]AAGACCCGCCAACAG	78514
rs583951051	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77464851	ACAGTGGCTCACAGC[A/C]ATCTGTAATGGGATC	78514
rs583966653	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77480479	CCTGGCTGTCCTGGA[A/G]CTCACTCTGTAGACC	78514
rs584027405	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77452736	TTTGTGTGAATGCAT[C/T]TAAATTGCTAAAAAA	78514
rs584039470	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77404910	TGCTGGGATTAAAGG[C/T]GTGTGCCACCAAGCC	78514
rs584051218	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77432095	AGGAGAGGAGAGGGA[C/T]AGAAAGACCAGGAAG	78514
rs584061538	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77275021	CTCAGTACAGGGGAA[C/T]GCCAGGGCCAAGAAG	78514
rs584073914	snp	C/T			intron-variant, downstream-variant-500B	Arhgap10	GRCm38.p3	8:77358135	CTCTCTCTCTCAAAA[C/T]GCCATCTCAGACCCT	78514
rs584078232	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77308148	CAGTATCCAAATCAA[C/T]AAAATCAGAAATGAA	78514
rs584081634	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77260995	CTGGGTCACTAACCA[C/T]CTCTTTCACACACAC	78514
rs584094206	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77306366	CATACAGGAAATCCA[A/G]GATATAATGAGAAGA	78514
rs584094832	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77278773	CTAGCTGTTGGAACG[G/T]AAGTCTTGAAAAGTG	78514
rs584134006	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77416342	CTATGCCATCAGAGA[C/T]GCCAACTTTCAGGAA	78514
rs584138398	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77457999	CTATCTATCTATCTA[C/T]CTATCTATCTACCTA	78514
rs584148617	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77460256	CAGCTAGCAGAGGAT[C/G]CACGGTATACAGCCT	78514
rs584150330	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77426632	CTTGCAGTGCTGTGC[A/G]CTCGTGAGGTCTTTC	78514
rs584160647	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77369763	TATGTCCCACATAGC[A/C]CGACTGTCCCACAGT	78514
rs584166029	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77387186	TTTTTAGTTTTTTTT[A/T]AATAATTATGTATCT	78514
rs584179726	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77337091	TGTCCTGGTTACTCA[C/T]GGACGGACAGACGGC	78514
rs584180217	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77299751	CAGATTGGGAAAGAA[A/T]TTTTACCAATTCTAA	78514
rs584182979	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77307582	TTCAAAATTGACCAT[A/G]TAATTGGTCACAAAA	78514
rs584184106	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77306475	ATAGAAGAAAACTTC[C/T]CTAACCTCAAGAAAG	78514
rs584185315	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77336011	ACACACACACACACA[A/C]ACACACACCTACCTA	78514
rs584249877	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77456929	CCTGAGTGAGGTAAC[C/T]CAATCACAAAAGAAC	78514
rs584251378	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77449089	CACTGCCACATCCCT[A/G]GCCCTGTGCACTCTG	78514
rs584266851	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10, 0610038B21Rik	GRCm38.p3	8:77515748	CTGAGGAGGAGGAAA[A/G]CTAGCCCCCCCCCCC	78514
rs584267772	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77261074	AGAGAGAGAGAGAGA[C/G]ACAGAGAGAGAGAGA	78514
rs584273717	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77295680	AATGAAGAAAATACC[C/T]AATAAAAATATTAAA	78514
rs584286809	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77382024	AGTAAGTTGCGTGTG[C/T]ACATAAGCTCAAGCG	78514
rs584288941	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77337860	CTATGTGGGTATGCT[A/G]GGTACCCACATACTT	78514
rs584301496	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77417045	AGTAACGAGCACAGG[A/G]AAAGGAGTCGTTGTT	78514
rs584317762	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77300234	AATGGGGTATAGAAC[C/T]AAACAAAGAATTCTC	78514
rs584352367	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77425332	AATTCCTTTCTGCTT[A/G]CATACTGAGGAGGAG	78514
rs584356985	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77411578	GACACACACGCACAT[A/G]CATACACACACACAC	78514
rs584370812	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77395789	AAGATAAGCCAATTA[A/G]TACATAATGACAGCA	78514
rs584374649	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77472155	ATACACACACATATA[C/T]ATATATATACACATA	78514
rs584376712	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77463742	GAATGCCAACAAGCA[A/G]TACCAGGTGAATAGT	78514
rs584390274	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77306433	GATTCCCAACTTAAA[A/G]GGACAATAAATATCT	78514
rs584395155	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77376212	AAGAAAAGCTGAAGA[A/G]TTCTTAACTGAAAAA	78514
rs584400673	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77324311	CGTGCTAAAAAGGTC[A/G]CACACACTCTCTCTC	78514
rs584419281	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77307867	AAAACTCATAGCTCC[A/G]AGTGCCTCCAAAAAG	78514
rs584435907	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77299340	ACCAATGGAATAGAA[C/T]TGAAGACCCAGAAAT	78514
rs584463549	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77511492	AGAGAGAGAGAGAGA[A/G]AGAGAGAGAGAAAAG	78514
rs584472464	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77499821	AGAGTCCCTCACCAG[A/G]TGAGGGACTGTATTA	78514
rs584475856	snp	A/G			intron-variant, utr-variant-5-prime	Arhgap10	GRCm38.p3	8:77493163	GGGAGAGGAGGAGGA[A/G]AAGGAGGAGGAAGAG	78514
rs584476471	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77445114	GCTGACAGCTTAAAC[A/T]GATAGGGAGTTGGTA	78514
rs584480366	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77461931	CTGTCTTTTATTTAC[A/G]TAACACATTTTCAAC	78514
rs584495376	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77325475	CTTCTGCTGCCCAGT[A/G]GGAGCGCTCTCCAGT	78514
rs584512045	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77418238	TCTCATGCCTCGCTC[A/G]ACATGGCTCAGTCCC	78514
rs584518654	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77300028	ATGGAAGATGGAAGA[A/T]GGAAGATGGAAGATG	78514
rs584520809	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77276178	CAATGCATACACACA[C/T]ACACACACACACACA	78514
rs584530149	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77511480	AGAAAGGAAGAAAGA[A/G]AGAGAGAGAGAGAGA	78514
rs584535380	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77489843	TAAAATTGCAGCTAG[A/G]ACCCAGGACAAATGA	78514
rs584603936	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77472522	TGTGTCTGAAGACAG[C/G]TACAGTGTACTCATT	78514
rs584606722	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77437515	GTCACAGAACAAAGC[A/G]AAGTGGGTAGTTCCA	78514
rs584608995	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77493303	GGAGGAGGAGGAGGA[A/G]GAGGAGGAGGAGAAG	78514
rs584611274	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77363072	CAACAACAGAATGAC[C/G]TCCTAACGTGCCTGT	78514
rs584611443	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77449133	CCTGTGCACACTGCC[A/G]CATCCCTGGCCCTGT	78514
rs584617411	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77382036	GTGTACATAAGCTCA[A/C]GCGTGCGCGCGCACG	78514
rs584619614	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77432375	CAATAGTCTCATCCC[A/C]GGTTCCAGGGCTTCG	78514
rs584625768	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77417876	ACATGCAAGCGTGCA[C/T]ACGTGAGGGCACACG	78514
rs584639550	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77368251	GCACCAGCCTTTTCT[C/T]CCAAAATTCTTTCTT	78514
rs584657519	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77307214	TAGCCATTTTAATAT[C/T]GACCAAAATGGAATT	78514
rs584661151	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77307227	ATTGACCAAAATGGA[A/C]TTTCAACCTAAAGTT	78514
rs584710409	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77496775	TGTTTGAAGCAAGGT[A/C]TCTCTCTATTTTACA	78514
rs584715063	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77407440	TAGAGATGGATGGAT[A/G]GATAATTAGATAAGA	78514
rs584715662	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77458019	CTATCTACCTACCTA[C/T]CTACCTACCTACCTA	78514
rs584732554	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77305942	AACACACCAGGAAAG[C/G]AAGACTCAGATTTAA	78514
rs584733874	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77367782	TTCAAACAAACTCGA[A/G]CATTTATGAAAAGTG	78514
rs584734003	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77316614	GCAGGGACAATGGGC[C/T]ATGGCCATTAAAACT	78514
rs584736302	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77455341	GTGATCAAGAAATGA[A/G]CCGGAGACACGGCCA	78514
rs584737426	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77386624	CAGGGCTGACCAGAG[C/T]GAGCAGAGGTCTTAA	78514
rs584745410	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77346227	GTCCAGCCAAGAACA[A/G]CAGCAGCACTGATGA	78514
rs584747638	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77253351	GCTCCCCTCTCCAGC[A/G]CTGGAATGGTGTGAA	78514
rs584754930	snp	A/G			intron-variant, utr-variant-5-prime	Arhgap10	GRCm38.p3	8:77493074	CCAGCCTGGTCTACA[A/G]AGCAAGTTGCCAAGG	78514
rs584763520	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77252665	CCATCTCAGGGCAGG[C/G]CCAGCGTTGTCAGGG	78514
rs584764491	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77332329	CTCTGAAGTTTGGTA[C/G]ATGCCATGCCAGATG	78514
rs584764805	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77287700	TTAATCCCAGCACTT[A/G]GGAGGCAGAGGCAGG	78514
rs584770057	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77305328	AGTGGGTAGGGGAGC[A/C]GGGCTGGGGGAGGGT	78514
rs584791196	snp	A/C			utr-variant-3-prime	Arhgap10	GRCm38.p3	8:77250902	CCACGATCAGTAGGA[A/C]CCCCCACGGCCGGGA	78514
rs584795078	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77501223	ACACAAAAGTGTCCA[C/T]TATCACAGGCTCACT	78514
rs584812709	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77489283	GTGTGTGTGTGTGTG[C/T]GTGTGCGCGCGTGCA	78514
rs584816895	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77451508	AGCTACAGACCCATC[A/G]CCTCCATTTTCCATG	78514
rs584821882	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77449205	CCTGGCCCTGTGCAC[A/T]CTGCCACATCCCTGG	78514
rs584835189	snp	C/T			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77485411	GAGGAAGGCAAGATG[C/T]CTGTCCTGTGGACGA	78514
rs584846514	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77421061	CACACGCGCACGCAT[A/C]CACACACAGGCGCAC	78514
rs584863038	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77401382	ATTGCTCCGACCCAT[A/G]GAGCACTGTCTTTCC	78514
rs584865483	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77421250	GCAGATCCCGGTATG[C/G]CACACATGGATGGAC	78514
rs584886862	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77274183	CTTGGTAAAATCAAA[C/T]GATTGGTGTGTGTGT	78514
rs584890983	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77299515	TTGTACAAAGCTCAA[A/G]TCTAAGTGAATCAAA	78514
rs584906957	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77333817	TTTCAGAGTCACCAC[C/T]GAGCTAATAAAGCTT	78514
rs584949599	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77447603	TGCCGCAGCTCACCT[A/G]CAGCTCCGCCCGTCT	78514
rs584951584	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77489277	GTGTGTGTGTGTGTG[C/T]GTGTGTGTGTGCGCG	78514
rs584953886	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77403019	ACACACAAAGACCTG[A/C]GTTGCTGATGAACAG	78514
rs584954705	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77382242	GACATATACACACAG[A/G]AGAGACATGTATGCA	78514
rs584955616	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77466144	TTTAATCTGGCTTTG[A/G]ATAATAAACAACACA	78514
rs584955848	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77426983	AAGCTTTTTTTCTGG[A/G]CTTTGCTACAAGTTG	78514
rs584957869	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77451136	CTCCTGCAGCTGACA[C/G]TGTGCATCTTTCCGC	78514
rs584969307	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77480560	GGATTAAAGGCGTGC[A/G]CCACCACACCTGGCT	78514
rs584974024	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77325831	TCAGAATCACCATAT[A/G]TTCACATATTCACAA	78514
rs584993273	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77312872	GCAAAGAAACATTGA[A/C]TTGGGAAGTCAACAG	78514
rs585008050	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77375013	TGAGCCCCATCCTAA[C/T]CCTCCGGTATCTTTC	78514
rs585021356	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77481101	GGTGGCCCACTGTCC[A/G]CGCTGACTGTCTACA	78514
rs585025801	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77448171	TGTGCGCATGCGCGC[A/G]CGCACACACACACAC	78514
rs585038430	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77504755	TGGCACACTGGCCAG[C/G]ATGGTCACAGTGCGA	78514
rs585072741	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77466900	CTCAGAAAGTAGAAG[C/T]TATAAAGTCACACAC	78514
rs585073434	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77414761	CATTTGTATTTGTTT[A/G]TTTGTTTGTTTATTT	78514
rs585114522	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77274281	TTCACTAAATTTGTT[A/G]TTCCTTTTTAATTTA	78514
rs585123644	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77307350	TTCATAAAAGCAACT[C/T]TAAGAAAGCTCAAAG	78514
rs585171767	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77433060	TGGCCCCGCAGCTCT[C/T]CACAGAACATCGAGG	78514
rs585178142	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77308356	AACGAAGTAAAAGCA[G/T]CCATTAAAGTCTCCC	78514
rs585183931	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77406367	TGACTAAATACTAAT[A/T]GTGTGTGTGTGTGTG	78514
rs585192888	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77477870	CAAGTAGAGCTTCTA[A/G]GAGGAGGAGTCACCC	78514
rs585196938	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77496533	CATGATGCTTTTTTT[C/T]CCCCCAAATGTGCCT	78514
rs585217413	snp	A/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77363463	GAGGAGGAGGAGGAG[A/G/T]AGACAGTGTCTCTAA	78514
rs585218882	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77425908	TTTGTTTGGGGCTTT[C/T]TTGGTTTTTTTTTTT	78514
rs585225061	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77413331	GGCAGCCCGTGGCTG[C/G]GGAGCTCCATGCTAC	78514
rs585237371	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77424028	ATGAGAAGGGGCCAC[A/G]TGCTGGTGGAAGGAG	78514
rs585242224	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77457564	AAGAGGTGAGAGTGG[A/G]TGTGAGAGGGTATGG	78514
rs585246364	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77369141	GGGTTTCTCTGTATA[A/G]CCCTGGCTGTCCTGG	78514
rs585259627	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77463741	AGAATGCCAACAAGC[A/C]ATACCAGGTGAATAG	78514
rs585280969	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77501989	CTCCTCTCTGTCCCC[A/G]GCTGTCCCCATGTAA	78514
rs585299487	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77458068	TATCTATCTATCTAT[A/G]CCAACACGTATTATC	78514
rs585314048	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77497003	ATGAGTTCAAGGCCA[C/G]TCTGGTCTACAGAGT	78514
rs585324500	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77404815	CAGGGATTCTCTGTA[C/T]AGCCCTGGCTGTCCT	78514
rs585349491	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77427987	TCCCTACACTGCACA[C/T]AGGAAAAGGGTATAA	78514
rs585351428	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77337445	ACACCCCTGCGCTAA[C/T]CTCCCCCTATTAGAA	78514
rs585358166	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77411535	ACACGTGTACACATA[G/T]ACACATGCACACACA	78514
rs585358472	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77371446	CAGACAAGAGCTGGG[A/G]AGATGGTTTAGTAAG	78514
rs585375667	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77277724	TCTATTGCTGCCACC[A/C]CCACCCCCAAGCCTA	78514
rs585381970	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77300049	ATGGAAGATGGAAGA[A/T]GGAAGAAGGAAGAAG	78514
rs585384217	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77308028	AAACAAACAAACAAA[A/C]AAAAAAAAAACTATA	78514
rs585408087	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77269116	TAGACAGACAGCCTA[A/G]GTCACAGGAGACAGA	78514
rs585423867	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77489292	TGTGTGTGTGTGCGC[A/G]CGTGCACATGAGCGT	78514
rs585443807	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77343068	TCCATCAGCAGTCAC[C/T]CCCTGTGGATGGAAA	78514
rs585447810	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77387003	AGAAAGAAAGAAAGA[A/G]AGAAAGAAAGAAAGG	78514
rs585456320	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77398598	AAGTCTTCATTTTGT[G/T]TTTTAAAAGACTGTA	78514
rs585465788	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77304866	TCCATGGAAGGAGTT[A/G]CAGAGACAAAGTTTG	78514
rs585469209	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77468286	CTGTGGGGCCACCTA[C/T]GCCTCTAAACTCACT	78514
rs585469382	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77387062	AAGGAAGGAAGAAAG[A/G]AAGAAAGAAAGAAAG	78514
rs585473342	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77355400	TAAGAAACATAGAGG[A/T]GGGGAGGGGAGGAAC	78514
rs585481868	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77452350	GTTTTTCGAGACAGG[C/G]TTTCTCTGTGTAGCC	78514
rs585481991	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77380919	CATTAGCCCGACTGT[A/G]CAGACTGAAACTCAA	78514
rs585486170	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77441297	CACTAATGCAGCAGC[A/G]AAGTCCACAACCCAT	78514
rs585491934	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77335959	AGAAAATTTGAATAT[A/G]ATAAATTCTCTCTCT	78514
rs585520973	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77299616	GCACAGGGGAAAAAT[A/T]CCTAAACAGAACAGC	78514
rs585570445	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77449349	CACTGCCGCATCCCT[A/G]GCCCTGTGCACACTG	78514
rs585575525	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77473158	GTGGTCGACAAGAAA[C/T]GGCTCAGCAGGGAGA	78514
rs585584129	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77511808	CAAAAAAAACAAAAA[A/C]AAAAAAAGAGTCGAA	78514
rs585585250	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77328039	TTTTGATGTTTAGGT[A/G]TGTTTTTTTCTTTTT	78514
rs585587913	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77511561	CATTGTTACCAGATG[A/G]CTTCATGTGGATGGA	78514
rs585589078	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77365404	CCCACAGTTATGAGA[A/C]CATGCTGAGGCACAG	78514
rs585594203	snp	A/C			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77485089	TTCCCCTCAGCTTCT[A/C]CCAGTCACTCACTTC	78514
rs585595264	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77383701	ATGATAAAGAGCAGA[A/G]ACAAAAAAAGGGGAA	78514
rs585602070	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77298656	ATCCATAATGAGATC[C/T]GATGCCCTCTTCTGG	78514
rs585606672	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77267223	GAAAGAGCACAGAAA[G/T]CATCCATGCCTGCAG	78514
rs585611550	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77306763	GGCTAATATACCCAG[C/T]AAAACTCTCAATTAA	78514
rs585616399	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77445247	AGGAAGGAAGGAAGA[A/G]AGAGAGAGAAAGAAA	78514
rs585616824	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77425692	AGAAGGAAGAAGAAG[A/C]AGAAGAAGAAGAAGA	78514
rs585628492	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77474678	TGAGAAAGTGGACCC[A/G]AAGAAGTGAAGCGGG	78514
rs585632074	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77495208	TAGGTTGGTAGAGTG[A/T]CTCTCTCTCTCTCTC	78514
rs585639319	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77457138	GTTTGGAGCTGAAAT[A/G]AAAGGATGGACCATC	78514
rs585652952	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77300339	ATAAAAACAACCTTG[A/T]GATTCCACCTCACAC	78514
rs585653130	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77282168	TAGTTAGTAGAATTC[A/G]GTGGTGGTGGTGGTG	78514
rs585705094	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77372684	ACAGACAGACTCACA[C/T]TGTCCCTCTGCTCTT	78514
rs585731227	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77369459	TTGTATACAAACAAT[G/T]GGCACAAATATGTAT	78514
rs585734894	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77298826	CAGCGCAGTAGCTGT[A/C]TATAAAATTAACTCA	78514
rs585761808	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77288429	GGTCTATTACCCTTA[C/T]ACACACACACACACA	78514
rs585778998	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77308268	GGATGAAATGGACAA[A/G]TTTCTAGACAGATAT	78514
rs585785914	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77497055	TACACAGAGAAACCC[A/T]GTCTCAGAAAGAAAA	78514
rs585797483	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77406689	TTTCTGAGGAGTTTG[C/T]ACTGATGTGGAAGGA	78514
rs585815462	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77463753	AGCAATACCAGGTGA[A/G]TAGTGTCTTTAATTT	78514
rs585817308	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77307427	ACTCTCAGCAATGGA[C/T]AGATCATGGAAACAG	78514
rs585817948	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77449401	CACTGCCGCATCCCT[A/G]GCCCTGTGCACACTG	78514
rs585825612	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77369247	GGTGTGCGCCACCAC[A/G]CCCGGTCATACTAGA	78514
rs585833325	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77274889	ATAGGTGGAACAACA[A/T]TATGAACTAACCAGT	78514
rs585848355	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77254507	AAAAGAAGGAAGGGG[A/G]AAGGGAAGGGGAAAG	78514
rs585903179	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77434149	GAGACCACCACACGC[C/T]GAAGAAGAGAACAAA	78514
rs585929528	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77453780	GCCCTGACTGTCCAG[C/G]CAAGGAGCTTCCCTT	78514
rs585935659	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77289734	GAAACTCTACTAAAG[C/T]GTAGCCACACAGGCT	78514
rs585946117	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77306136	GAACAAAACCATCCA[A/G]GATCTAAAAATGGAA	78514
rs585946572	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77457095	GAATTGGGAGCAAGG[C/T]ACCCATGGAAGGAGC	78514
rs585950094	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77322091	CTCTCTCCGCTTCCA[C/T]AGCCAACGTGCCACA	78514
rs585963524	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77255333	ACAGCTGGCCACCCA[C/T]ACTACAGTGCATCAT	78514
rs585964690	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77306050	GGTAAATAGGTAAAA[A/G]CCCTTAAAGAGGAAA	78514
rs585979800	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77412402	TTTTTTTTTTTGGAG[A/G]TGGGGGAGGAGGGTG	78514
rs585996780	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77373368	ATTCAGAAAAATCTA[A/T]AAACAAACTCACTGC	78514
rs586004661	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77398165	TTCTTTTTTTTTAAA[G/T]ATTTATTTATTTATT	78514
rs586006663	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77425571	GAGGAGGAGGAGGAA[A/G]AGGAGGAGGAGGAGG	78514
rs586015038	snp	C/G			intron-variant	Arhgap10	GRCm38.p3	8:77491282	ATAAAATAAATAAAT[C/G]TTAAAAAAAAAATTA	78514
rs586042198	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77387127	AGAAAGGAAGGAAGA[A/T]AGAAAGATTGATTCA	78514
rs586047676	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77486042	AGAACATGAGGAACT[A/G]TATTAAAGAGTAGCA	78514
rs586056415	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77422817	CTGCTGCAACAGCCC[C/T]ACTCTCCTCGTATCA	78514
rs586066968	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77335988	CTCTCTTTCTCTCAC[A/T]CACACACACACACAC	78514
rs586070036	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77297195	CTCAAATTTGAACAT[A/T]CCTTTTTAATTGATT	78514
rs586077434	snp	A/C			intron-variant, downstream-variant-500B	Arhgap10	GRCm38.p3	8:77358296	GCCATACCTGCCTGC[A/C]TGCTACCGTGCTTCT	78514
rs586106294	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77253643	TGTCTTGAGGATTTC[A/G]TTCCGTCTCCTTCCC	78514
rs586114976	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77417655	AAAAAAAATTAAAAA[C/T]CACAAGAGAATAAGA	78514
rs586115490	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77378698	ACAAAGGAGAATGCT[A/G]AGCCATCATCTCTCT	78514
rs586135964	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77306041	GAGAACACAGGTAAA[C/T]AGGTAAAAACCCTTA	78514
rs586138131	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77299660	GTAAGATCAGGAATT[A/G]ACAAATGGGACCTCA	78514
rs586139581	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77319125	ATATGCCCTAGTACA[A/G]GGGAACGCCAGGGCC	78514
rs586141676	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77274957	AGAAGATGGCCTAGT[C/T]AGCCATCAGTGGAAA	78514
rs586141968	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77449114	ACTCTGCCGCATCCC[C/T]AGCCCTGTGCACACT	78514
rs586143596	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77347951	CTCTCAGAGCTCTGT[A/G]TGTGTGTGTGTGTGT	78514
rs586153259	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77452697	CTAACAAAGAAGAGC[C/T]ACACACCCGTCAGTC	78514
rs586164215	snp	A/G			intron-variant, upstream-variant-2KB	Arhgap10	GRCm38.p3	8:77493911	GAGGTAGAGTAATTT[A/G]AGCAAAGTAATAGAG	78514
rs586168446	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77300014	GAAAGAAGAAGAAGA[A/T]GGAAGATGGAAGATG	78514
rs586169595	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77481149	CTGTCCACACTGACT[A/G]TCTACACATGAAATG	78514
rs586184385	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77336755	CCAGGGCGGAGCTTC[A/G]TCCCGGGTGAGGAGC	78514
rs586283164	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77443341	TTGTATGGTCAGTCA[C/T]GGGGAAGCCCACAGT	78514
rs586288881	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77509480	AAATAGAGGAGGGGC[A/T]GGAAGAGAAGGAAGG	78514
rs586301073	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77468785	AATAATTGCTGTCAT[A/G]TTAATTTCCAGCATT	78514
rs586301807	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77380153	ACTAAAGGTAGTACG[C/T]GTGCACCCTGTTTCT	78514
rs586305063	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77489842	TTAAAATTGCAGCTA[A/G]AACCCAGGACAAATG	78514
rs586307676	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77411396	CACACAGACACACGC[A/G]CACATGTGTACACAC	78514
rs586311876	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77427045	TGTTTTTGATCCTAA[C/T]AACCCTAAGACCTTC	78514
rs586323446	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77369770	CACATAGCACGACTG[A/T]CCCACAGTCTGCTCT	78514
rs586323783	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77481088	CTACACATGAAATGG[C/T]GGCCCACTGTCCACG	78514
rs586327838	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77496945	GGCAGTGGTAGCGCA[C/T]GCCTTTAATCCCAGC	78514
rs586328774	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77320324	GGGTTACACAGAGAA[A/G]CCCTGTCTCAAAAAT	78514
rs586329827	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77387204	TAATTATGTATCTGT[A/G]TGAGAGTGTGTGTGT	78514
rs586337877	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77458031	CTACCTACCTACCTA[C/T]CTACCTACCTATCTA	78514
rs586343751	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77464895	TAGTGTGTCTGAAGA[C/T]AACTACTAGTATACA	78514
rs586363931	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77468120	TCCTCCTGCACTGAC[A/C]CCCCTCCTCCTTGCA	78514
rs586374583	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77352686	ACACACACACACACC[A/C]CAAATAATGCCAGGG	78514
rs586382311	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77469515	GAACCGCAGACATTT[A/G]TTCTTGCCTCCCAAG	78514
rs586400573	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77434460	AATATAAAAATAGTT[A/C]ATAGAAATATATAAC	78514
rs586416672	snp	C/T			upstream-variant-2KB, downstream-variant-500B	Arhgap10, 0610038B21Rik	GRCm38.p3	8:77518923	TCTTTAAAAACGTTC[C/T]GACTGAGTGCAGTAA	78514
rs586435773	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77283183	AGGAGGAGGGAGGGG[A/G]AGGGGGGAGGGAGGA	78514
rs586438306	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77300755	GCAAATGGATGTATC[C/T]GGAGGATATCATCCT	78514
rs586439730	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77306673	TTGTACCAGACTTCT[C/T]ACCAGAGACTATGAA	78514
rs586449731	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77308305	CCAAAGTTAAATCAG[A/G]ATCAGATAAACCATC	78514
rs586453616	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77341890	TGTTAACTTCTCAGG[A/G]AAAAAAATAAAAATA	78514
rs586483794	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77367841	ATGTCGCTTCAGCAA[C/T]GTTAATCACTGAGCT	78514
rs586503590	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77425701	AAGAAGAAGAAGAAG[A/C]AGAAGAAGAAGCAAA	78514
rs586511735	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77307217	CCATTTTAATATTGA[A/C]CAAAATGGAATTTCA	78514
rs586512930	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77405337	ATCCATCACACTCAT[A/T]CCCAAACCGCTGGGC	78514
rs586514720	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77443581	CCTAGACACCATGTT[C/T]AAAGAACACCTGCTG	78514
rs586515347	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77399397	CTCAATGCCTTTGTG[A/C]CCCTGGAAACATTAA	78514
rs586516020	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77432356	GGAAAATATGTCCCA[A/G]TAGCAATAGTCTCAT	78514
rs586519004	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77423409	GAGAGGTGGGTTCCG[A/G]GGGTTGGGGGTCTGA	78514
rs586524988	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77411450	TGTGTACACATGCAC[A/G]CACATGTATACACGT	78514
rs586525606	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77272651	CTTTTTTTGCTATTT[C/T]TCTTCCCACTCTCCT	78514
rs586531013	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77382032	GCGTGTGTACATAAG[C/T]TCAAGCGTGCGCGCG	78514
rs586537306	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77453810	TCCCAGACACCCCTT[A/C]CTGCAGGAGGTGTTT	78514
rs586538189	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77471061	TACGGATGGTTGTGA[A/G]CCACCATGTGGTTGC	78514
rs586555218	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77307638	TGAAATAATCCCATG[C/T]ATCCTATGAAATCAC	78514
rs586593635	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77457272	TCTCATGTGAGACTA[G/T]GCCGGGGCCTAGCAA	78514
rs586601444	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77498803	AGATAATCAAATGAG[A/C]GGGTCAAGAGCTCTT	78514
rs586612352	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77495300	CCTCCCTCCCCCTCC[C/T]TCCCTTCTCTCTCTC	78514
rs586623201	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77511090	AAAGCTAGAGGACCG[A/G]TCTGTAAGCCACAAC	78514
rs586652242	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77307015	TATTCCTTAATATCT[C/T]TTAATATCAATGGAC	78514
rs586671998	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77299109	AAAGCAAACTACAGA[C/T]TCAATGCAATCCCCA	78514
rs586695874	snp	A/G			downstream-variant-500B	Arhgap10	GRCm38.p3	8:77250073	GACAAAGCCATACTC[A/G]GTGGTATGAGAGAGA	78514
rs586708924	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77476299	GTATTAAAAATGCAT[A/G]ACAATGCTACATTCC	78514
rs586729491	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77487532	GAAGAACTGTAGGCA[C/T]CCTTCACCGCAGACG	78514
rs586743973	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77251542	CCACTCCCACACTGG[G/T]TAGGGAGTTCCTGAA	78514
rs586746347	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77305279	CTTTATATGCCCCAA[C/T]ACAGGGGAAAGCCAG	78514
rs586756760	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77407418	AGTAGATAGATAGAT[A/G]GATAGATAGAGATGG	78514
rs586770222	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77366719	CCCACACGATCGTTT[C/T]CTTTTTACTTCTTCC	78514
rs586774267	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77386245	AAAAAAGGGATTAAA[A/G]GATTAGCAGAACTAG	78514
rs586775286	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77450582	GCTCAGAAAACCCCA[C/T]CCCCTCAAAGCACTA	78514
rs586788027	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77514664	TGTGCTCAAGTGCTG[A/G]CCTGGCTCTCGCTCC	78514
rs586806655	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77405587	CTCACTAGAGTTTGC[A/G]TCACAGGAGTAACAC	78514
rs586822035	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77323305	CTCCTCCCAATTTCA[C/T]ACACTGAACTCCAGG	78514
rs586843833	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77290213	CAAGTCCATAACAAA[A/G]CAAAACAAAACAAAC	78514
rs586844264	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77457569	GTGAGAGTGGGTGTG[A/G]GAGGGTATGGGGGAC	78514
rs586868224	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77496534	ATGATGCTTTTTTTC[C/T]CCCCAAATGTGCCTG	78514
rs586878933	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77386627	GGCTGACCAGAGTGA[A/G]CAGAGGTCTTAAAAT	78514
rs586884117	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77446531	CACTGCATGGGGGTA[A/G]TGCATGCCTACAGCC	78514
rs586888406	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77299394	TGATCTATGACAAGG[A/G]ACCTAAAACCATCCA	78514
rs586888635	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77407881	AAAGGAGCAGTTTTT[A/G]CTATATATATTAAAA	78514
rs586891942	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77471984	TTGGCCACCCAACAA[A/G]TGTCCGCGTCTTCCC	78514
rs586942814	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77443756	GAGGCAGAAGCAGGC[A/G]GATTTCTGAGTTCGA	78514
rs586979477	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77475214	GAAAGAGAGACGCCA[A/T]GGAGTAGGTGAATCG	78514
rs586982666	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77420950	CCCAAACTCTAGAGA[A/C]GAGCTTGATGACCCT	78514
rs586993294	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77488063	AAGGGCATCATCCTC[A/G]GCACACTGCTACCAA	78514
rs587026209	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77275281	AGAGAGAAAGAGAGA[A/G]AGAGAATACATGCAG	78514
rs587034339	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77284057	GTAGCCTTAATTAGC[C/T]AGTACTACACACACA	78514
rs587038291	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77305237	AGTCAGCCATCATTG[A/G]GAAGAGAGGCCCCTT	78514
rs587055954	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77306382	GATATAATGAGAAGA[A/C]AAAACCTAAGAATAA	78514
rs587061972	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77404911	GCTGGGATTAAAGGC[A/G]TGTGCCACCAAGCCT	78514
rs587110043	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77457534	TATGCCTCAGTACAG[G/T]GGAACGCCAGGGCCA	78514
rs587120628	snp	A/G			intron-variant, utr-variant-5-prime	Arhgap10	GRCm38.p3	8:77493078	CCTGGTCTACAAAGC[A/G]AGTTGCCAAGGCAAC	78514
rs587144460	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77306979	AAAATAACATCAAAA[A/G]TAACAGGAAGCAACA	78514
rs587146429	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77285250	ATACGCGTGTGCGTG[C/T]GTGCGTGCGTGTGTG	78514
rs587151867	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77407358	GATAGATAGATAGAT[A/G]GATAGATAGATAGAT	78514
rs587158818	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77431130	CACGCACGTGTGCAC[A/G]CACCCCCCCTAAACT	78514
rs587212776	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77425710	AAGAAGAAGAAGAAG[A/C]AGCAAACTCAGCCTA	78514
rs587219443	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77412746	TAAGCAGCTTCCCAG[A/G]CCACAGCAGGCTATC	78514
rs587245796	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77447051	GTTTTGGTTTGGTTT[G/T]GTTTAAGGGGGGGAG	78514
rs587251704	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77345013	TCCCCTTCCCTGCTC[G/T]CCAGTCTTCCTTCTC	78514
rs587262284	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77258172	GCAGTAAGCAGCATT[C/T]CTCCATGGCTTCTGT	78514
rs587268989	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77306299	ATACCATAGAAAACA[C/T]TGACACAACAGTCAA	78514
rs587281394	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77491847	ATGCCCTCACCCCCG[A/G]CCCCCGACAGCAGCA	78514
rs587297868	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77441155	GGAAAGGAGAGGGGA[A/G]GCCGAGATGGTAACA	78514
rs587298270	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77511471	AAAAGAGAAAGAAAG[A/G]AAGAAAGAGAGAGAG	78514
rs587310889	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77454982	AGCCATGGAACTTAC[A/G]AAGCTAGACACTGGT	78514
rs587342835	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77300035	ATGGAAGATGGAAGA[A/T]GGAAGATGGAAGAAG	78514
rs587348650	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77356080	ATATTATATATAGGA[C/T]CAAATAATTCCTTAC	78514
rs587353715	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77381517	CGTGAGTATGGGGCC[A/G]CCGGACTGGCTTCAG	78514
rs587355057	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77307953	AAAAAGAAGCAAATA[A/C]ACCCAAGAAGAGCAG	78514
rs587402942	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77261068	AGAGAGAGAGAGAGA[A/G]AGAGAGACAGAGAGA	78514
rs587407415	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77299855	CACCTTTAATCCCAG[A/C]ACTGGGGAGGCAGAG	78514
rs587407548	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77307588	ATTGACCATATAATT[A/G]GTCACAAAACAGACC	78514
rs587415223	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77336055	CTTTCTAATTTGAAG[C/T]ATTTCTTTATTTGTA	78514
rs587423075	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77430478	GCCTCGAAGTAAACT[C/T]CCACCAGCACCATTA	78514
rs587425424	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77323996	CCTCCACCCCCCCCA[G/T]CCCCTCCACCCCTTC	78514
rs587427715	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77415988	CAGCAATGGGAGTGT[A/G]CTTCCCACCTCTTGT	78514
rs587428955	snp	G/T			intron-variant	Arhgap10	GRCm38.p3	8:77275022	TCAGTACAGGGGAAC[G/T]CCAGGGCCAAGAAGT	78514
rs587436240	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77337104	CACGGACGGACAGAC[A/G]GCCTTTGGGTTTTGT	78514
rs587440974	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77460171	CCAAAGGAGTCGGGG[A/G]TTGGGGAGCACAGGT	78514
rs587444007	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77448725	CACTGCCGCATCCCT[A/G]GCCCTGTGCACACTG	78514
rs587477511	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77511484	AGGAAGAAAGAGAGA[A/G]AGAGAGAGAGAGAGA	78514
rs587485601	snp	A/C			intron-variant	Arhgap10	GRCm38.p3	8:77269729	AGAAACCAAACCAAA[A/C]CAAACAAACAAAAAA	78514
rs587489911	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77299003	CTTCAAGTGTCTGAA[A/G]AAAGAAATTAAAGAA	78514
rs587566428	snp	A/T			intron-variant	Arhgap10	GRCm38.p3	8:77460380	ATATGAAAACTAGAA[A/T]AGAGGTACAAAGTAG	78514
rs587569285	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77448751	CACTGCCGCATCCCT[A/G]GCCCTGTGCACACTG	78514
rs587571543	snp	A/G			intron-variant	Arhgap10	GRCm38.p3	8:77497159	TGTATGTGTTTTGCT[A/G]GAGTGTATGTATGAG	78514
rs587573469	snp	C/T			intron-variant	Arhgap10	GRCm38.p3	8:77481171	CATGAAATGACCGTC[C/T]ACTATTCACACTGAC	78514
rs864265900	snp	A/C/G			intron-variant	Arhgap10	GRCm38.p3	8:77299116	ACTACAGATTCAATG[A/C/G]AATCCCCATCAAAAT	78514
rs864272104	snp	C/G/T			intron-variant	Arhgap10	GRCm38.p3	8:77279344	GTTCTCTTCTGCAAG[C/G/T]GAGCGAGCGAGCACA	78514
rs864302656	snp	A/G			synonymous-codon	Arhgap10	GRCm38.p3	8:77411034	TACCAGTTTCCCCCC[A/G]GATCTGTGCTCAAAT	78514
rs864306562	snp	A/C/G			intron-variant	Arhgap10	GRCm38.p3	8:77425478	GAGGAGGAGCAGGAG[A/C/G]AGGAGGAGGAGAAGG	78514
rs864316166	in-del	-/GTAA			intron-variant	Arhgap10	GRCm38.p3	8:77453844	CTCTGTTCACCCTGG[-/GTAA]GTAAGCCTATGCATC	78514
rs864319829	in-del	-/GTAA			intron-variant	Arhgap10	GRCm38.p3	8:77453845	TCTGTTCACCCTGGG[-/GTAA]TAAGCCTATGCATCC	78514

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