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
rs9724	snp	C/G	0.0700422	0.173537	utr-variant-3-prime, nc-transcript-variant	ARHGAP10	GRCh38.p7	4:148072706	TCGGTGCTCCTCACC[C/G]GTGTGCTGTTTTCCA	79658
rs168367	snp	A/G	0.0941369	0.195465	intron-variant	ARHGAP10	GRCh38.p7	4:147935156	TTAATCACAACAGAC[A/G]GCTCGACCATCACCC	79658
rs168368	snp	C/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147945091	GCTGGGCTTACACGC[C/T]TCTAACAACCTGGCC	79658
rs180952	snp	C/T	0.180702	0.240204	intron-variant	ARHGAP10	GRCh38.p7	4:147932728	ggtttgctgcacaga[C/T]catcccattactcag	79658
rs182989	snp	C/T	0.104149	0.203046	intron-variant	ARHGAP10	GRCh38.p7	4:147930597	ATTTCACAGGAATTG[C/T]TGAGTACTTATATTT	79658
rs187005	snp	C/T	0.161924	0.233971	intron-variant	ARHGAP10	GRCh38.p7	4:147934906	CCCACAGTGATACTC[C/T]CTTCTTCTAAACATA	79658
rs187006	snp	A/T	0.438666	0.164028	intron-variant	ARHGAP10	GRCh38.p7	4:147945437	AGTTTTCTTTATCCA[A/T]ATAGCGTGTAATTAT	79658
rs187007	snp	G/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147943090	CATGAACTATTGTAA[G/T]TGATATTTTACATTC	79658
rs238866	snp	C/T	0.0810805	0.184299	intron-variant	ARHGAP10	GRCh38.p7	4:147926433	tcgttttcactttcc[C/T]ctctccctgacttcc	79658
rs349023	snp	A/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147917134	ATCCTTTGATTCAGG[A/T]GTAGGATAGCTCTCA	79658
rs349024	snp	C/T	0.0402882	0.136092	intron-variant	ARHGAP10	GRCh38.p7	4:147933716	ATCCATCTGGGCCAC[C/T]AGAACAGTCTTCTGG	79658
rs349025	snp	C/T	0.104504	0.2033	intron-variant	ARHGAP10	GRCh38.p7	4:147930394	TTAGCCTATGGTATA[C/T]ATTTAACAAATGAAT	79658
rs731989	snp	A/G	0.0839998	0.186933	intron-variant	ARHGAP10	GRCh38.p7	4:147863500	CCAATGCCCATGGAT[A/G]GATGGATGAGTAAAT	79658
rs744031	snp	C/T	0.287606	0.247155	intron-variant	ARHGAP10	GRCh38.p7	4:147810833	TTCCTAAAGCCATCA[C/T]GACAGGGTCTGTCAC	79658
rs747097	snp	C/T	0.465892	0.126058	intron-variant	ARHGAP10	GRCh38.p7	4:147809674	GGTCCCCAACCTTTT[C/T]GGCACCAGGGACTGG	79658
rs869762	snp	C/G	0.26326	0.249648	intron-variant	ARHGAP10	GRCh38.p7	4:148005323	GTGTGCTGGCTCATG[C/G]CTGAAATCTGATCAC	79658
rs869763	snp	A/C	0.266	0.249487	intron-variant	ARHGAP10	GRCh38.p7	4:148005327	GCTGGCTCATGGCTG[A/C]AATCTGATCACTTTG	79658
rs869764	snp	C/G	0.26271	0.249677	intron-variant	ARHGAP10	GRCh38.p7	4:148005929	GAGATACATGTATTT[C/G]TTTCACCTAATATTG	79658
rs893022	snp	A/G	0.447162	0.153712	intron-variant	ARHGAP10	GRCh38.p7	4:147832084	GTGTGTGTATGTCGG[A/G]CGGGGCAGTCAGGGG	79658
rs893023	snp	C/T	0.238171	0.24972	intron-variant	ARHGAP10	GRCh38.p7	4:147831208	CGAAACAATTTAGAG[C/T]GTATCCAACGTCCAG	79658
rs893024	snp	A/G	0.391954	0.205789	intron-variant	ARHGAP10	GRCh38.p7	4:147843101	GAAGCCCACAAACCC[A/G]TTTGTACTGGGCACC	79658
rs893025	snp	A/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147943159	TGTTTTAAACTAAAG[A/T]AGGGAAGAAGGAAGA	79658
rs893026	snp	A/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147811057	CCACAGGAAAAAGAG[A/G]ATTAAGGCGAGGAGC	79658
rs893030	snp	A/G	0.136166	0.22258	intron-variant	ARHGAP10	GRCh38.p7	4:147863400	tactacaacatggat[A/G]aaccttgaggacatc	79658
rs893031	snp	A/T			intron-variant	ARHGAP10	GRCh38.p7	4:147862671	CAGTCAACCTCTATC[A/T]CCACCCCCTTAATGT	79658
rs893032	snp	C/T	0.0505692	0.150756	intron-variant	ARHGAP10	GRCh38.p7	4:147899332	gtgtgtgcatgcgtg[C/T]gtgtgtgtgtgtctg	79658
rs893033	snp	A/G	0.41408	0.188621	intron-variant	ARHGAP10	GRCh38.p7	4:147899481	TTTCATAGGTTCTCC[A/G]TCTTGTTCTTATTGG	79658
rs893034	snp	A/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147899561	caACAGTTCTCTAAT[A/G]ATTAATTGCTTGAAT	79658
rs906124	snp	C/T	0.487621	0.0776941	intron-variant	ARHGAP10	GRCh38.p7	4:148069209	CAGCCTTATCTGCAA[C/T]TGCGGAGCCACTTTT	79658
rs906125	snp	A/T	0.487809	0.0771174	intron-variant	ARHGAP10	GRCh38.p7	4:147924039	CCTCCCACAGAAGAC[A/T]GTCCTCTATTTCCAC	79658
rs924780	snp	A/C	0.487495	0.0780784	intron-variant	ARHGAP10	GRCh38.p7	4:147764846	TAAAACACACTTAAT[A/C]AATGTTTACTGGGCT	79658
rs924781	snp	C/T	0.00159617	0.0282053	intron-variant	ARHGAP10	GRCh38.p7	4:147757774	CCGAAACAAGGACAA[C/T]GGTAATTAGCTGGGC	79658
rs924782	snp	A/G	0.00159617	0.0282053	intron-variant	ARHGAP10	GRCh38.p7	4:147757643	AGTAAGCCAATGTTC[A/G]GAGGAAGCAGAGGCT	79658
rs924784	snp	G/T	0.00279162	0.0372561	intron-variant	ARHGAP10	GRCh38.p7	4:147740511	CAGTCATCATACTAA[G/T]GTAAAAAGAATATCC	79658
rs937020	snp	A/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147931297	TCTCTTAATAAATTA[A/G]ATTGAGATTCGTTCT	79658
rs964170	snp	A/C	0.434976	0.168179	intron-variant	ARHGAP10	GRCh38.p7	4:147774805	AGACTCTGTCAATGA[A/C]AAAATGTTCTTCTCA	79658
rs969032	snp	A/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147955286	CAGCTCAGAATTATC[A/G]AATAAATCCAAACAA	79658
rs975371	snp	C/T	0.34303	0.232046	intron-variant	ARHGAP10	GRCh38.p7	4:147923075	AATTGTTGAGACACA[C/T]AATATTACCAATATG	79658
rs975372	snp	C/T	0.342806	0.232136	intron-variant	ARHGAP10	GRCh38.p7	4:147922932	ATAAGACATTTTCTC[C/T]GAGTAAACAGTAAAG	79658
rs988112	snp	A/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147866362	TGACACAATCTTTAA[A/G]AAAGTAAAATCACAG	79658
rs990245	snp	A/C	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147956457	ATGTGAAAACAAAAA[A/C]GAATAGAACCAGTTT	79658
rs992572	snp	C/T	0.0275645	0.114116	intron-variant	ARHGAP10	GRCh38.p7	4:148039488	TATTTTTAGTAAAGA[C/T]GAGGTTTCACTGTGT	79658
rs1013842	snp	A/G	0.418169	0.184985	intron-variant	ARHGAP10	GRCh38.p7	4:147862251	ggcaacagtacctgg[A/G]cttggctacaacttt	79658
rs1021956	snp	G/T	0.240478	0.249819	intron-variant	ARHGAP10	GRCh38.p7	4:148058023	CTCGGTGTGCTCGTG[G/T]GGAGCCAAACAATGT	79658
rs1036441	snp	C/T	0.145642	0.227177	intron-variant	ARHGAP10	GRCh38.p7	4:147909102	taaattgggggttcc[C/T]gtgaacccctcatca	79658
rs1036444	snp	G/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147940014	CAAAAAACTCCTGTA[G/T]AAAGTATAGGAATGG	79658
rs1039660	snp	C/T	0.29432	0.24604	intron-variant	ARHGAP10	GRCh38.p7	4:147973402	CCAACTATGTACCCA[C/T]GAAAATTAAAAATAA	79658
rs1113688	snp	G/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147732709	ACCAGGCGGGGCCCA[G/T]GCGGGGCCCGCTGGC	79658
rs1119887	snp	C/T	0.272241	0.249009	intron-variant	ARHGAP10	GRCh38.p7	4:147803955	ccagcattcccacta[C/T]cgaatatttatccaa	79658
rs1161575	snp	G/T			intron-variant	ARHGAP10	GRCh38.p7	4:147778549	CCCTGCTCTAGGGCT[G/T]TAACAAAACTGAAAT	79658
rs1161576	snp	G/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147778525	CTGAAATATGAAAAA[G/T]GGCTGTGAAAGACCC	79658
rs1161577	snp	A/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147807162	ACCTCAAGGGAAGCA[A/T]AATATGTCACACAGT	79658
rs1177326	snp	A/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147803332	tttctttttttattg[A/G]tacataactgtacat	79658
rs1182742	snp	G/T			intron-variant	ARHGAP10	GRCh38.p7	4:147790271	aataattccataagg[G/T]gggcttcacctttgt	79658
rs1183548	snp	C/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147774425	CCCAGGTCATGTTTT[C/T]CACCTGCACACTCTT	79658
rs1185058	snp	G/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147774492	TTGACTTCAAAATTG[G/T]CCTTATATAACCCTT	79658
rs1185059	snp	G/T			intron-variant	ARHGAP10	GRCh38.p7	4:147790130	agtccaaaatcaagg[G/T]gctggtatattcggt	79658
rs1185487	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147790122	ggctgggaagtccaa[A/G]atcaaggggctggta	79658
rs1317354	snp	A/G	0.266	0.249487	intron-variant	ARHGAP10	GRCh38.p7	4:148005306	ATACATATATAAGCT[A/G]GGTGTGCTGGCTCAT	79658
rs1347596	snp	A/G	0.427119	0.176434	intron-variant	ARHGAP10	GRCh38.p7	4:147838927	TATCTGAAACTAAAT[A/G]TGATTAGGGCTATTT	79658
rs1369958	snp	A/C	0.278399	0.248382	intron-variant	ARHGAP10	GRCh38.p7	4:147903580	tcatacagaagattt[A/C]actgccctaaaaatc	79658
rs1369959	snp	G/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147927500	TGAGAGAGTGTGAGA[G/T]ACTCCAAAAACATAA	79658
rs1395296	snp	C/G	0.0696718	0.173152	intron-variant	ARHGAP10	GRCh38.p7	4:147993423	TATCAGGTCATTTAA[C/G]TATTGTTATGAATAA	79658
rs1436489	snp	A/G	0.265453	0.249522	intron-variant	ARHGAP10	GRCh38.p7	4:147840563	TGCTTACCTTGTTTG[A/G]ATTCAGGCGGTATGT	79658
rs1436490	snp	C/G	0.239037	0.24976	intron-variant	ARHGAP10	GRCh38.p7	4:147844325	GTTCAAGCATTTATC[C/G]TTTGTGTTACAATCT	79658
rs1436491	snp	G/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147951830	caaacttaccgaaac[G/T]tacactataaatata	79658
rs1436492	snp	A/G	0.0513262	0.151752	intron-variant	ARHGAP10	GRCh38.p7	4:147951792	tattgtatgtcaact[A/G]tgtttcaataaagct	79658
rs1436493	snp	A/G/T	0.000399281	0.0141238	intron-variant	ARHGAP10	GRCh38.p7	4:147940007	CTCCTGTATAAAGTA[A/G/T]AGGAATGGAATGACA	79658
rs1469865	snp	C/T	0.415727	0.187175	intron-variant	ARHGAP10	GRCh38.p7	4:147860045	GAGCATCTCAATTCA[C/T]TGAAAATTAGCATTA	79658
rs1469866	snp	C/G			intron-variant	ARHGAP10	GRCh38.p7	4:147860018	ATTACATTAACCACT[C/G]CCAAAAGTAATGAAT	79658
rs1469867	snp	G/T	0.455024	0.143057	intron-variant	ARHGAP10	GRCh38.p7	4:147859979	CTAACATTTTCCCCT[G/T]TAAAAAGCATCCCCC	79658
rs1469868	snp	C/G			intron-variant	ARHGAP10	GRCh38.p7	4:147859640	caagaagcttacatt[C/G]tagtggaagaagcca	79658
rs1529935	snp	C/T	0.47802	0.102502	intron-variant	ARHGAP10	GRCh38.p7	4:147909321	tcatgttcaccaaca[C/T]ggaagctTATCAGAG	79658
rs1529939	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147909577	gatgctctgtgtcag[A/G]aAGTGGGGATGCAGA	79658
rs1567062	snp	C/T	0.499382	0.017561	intron-variant	ARHGAP10	GRCh38.p7	4:147993952	gatacatcaatacta[C/T]ctaccctttcagggt	79658
rs1583541	snp	G/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147927502	TGTGAGAGAGTGTGA[G/T]AGACTCCAAAAACAT	79658
rs1604785	snp	A/G	0.440057	0.162414	intron-variant	ARHGAP10	GRCh38.p7	4:147803487	ttgttattttgaaat[A/G]tttttaattatagtc	79658
rs1811406	snp	C/T	0.394721	0.203852	intron-variant	ARHGAP10	GRCh38.p7	4:147893064	TTGAATGGAAGTAAA[C/T]ttttttttttttgag	79658
rs1811407	snp	C/G			intron-variant	ARHGAP10	GRCh38.p7	4:147893150	tgcaacctctgcctc[C/G]tgggttctagcgatt	79658
rs1873175	snp	A/C	0.3744	0.216852	intron-variant	ARHGAP10	GRCh38.p7	4:148004638	ctgactatgggctgg[A/C]ggctgcctcagctcc	79658
rs1876196	snp	C/T	0.000798403	0.0199641	intron-variant	ARHGAP10	GRCh38.p7	4:148071353	gggagtggtggctca[C/T]gcctgtaatcccagc	79658
rs1966686	snp	A/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147853099	TCTGAGCTGCTGAAA[A/T]GGGCTCTAGCCACCT	79658
rs1969102	snp	A/G	0.43978	0.162738	intron-variant	ARHGAP10	GRCh38.p7	4:147738482	GGCGTGGACCCAGGA[A/G]GTGGAGCTTTCAGCG	79658
rs1969103	snp	A/C	0.451732	0.147663	intron-variant	ARHGAP10	GRCh38.p7	4:147738560	TCTGTCTCCCCCCCC[A/C]AAAAAAAATTATAAT	79658
rs1969104	snp	A/G	0.0275645	0.114116	intron-variant	ARHGAP10	GRCh38.p7	4:147757258	GCAGTGAGCCCAGAT[A/G]GCACCACTGCACTCC	79658
rs1971125	snp	C/T			intron-variant	ARHGAP10	GRCh38.p7	4:147835403	ttttcccttaagtct[C/T]gctctgtcgcccagg	79658
rs2015429	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147940030	AATTGTCTCTGCTCA[A/G]CAAAAAACTCCTGTA	79658
rs2015431	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147940027	TGTCTCTGCTCAACA[A/G]AAAACTCCTGTATAA	79658
rs2017857	snp	C/G	0.416218	0.186739	intron-variant	ARHGAP10	GRCh38.p7	4:148067248	CTTACTGTACCCTTT[C/G]AAGAAGTGTTCCTAT	79658
rs2043643	snp	C/G	0.413748	0.188909	intron-variant	ARHGAP10	GRCh38.p7	4:147898772	cctgtcttcttctga[C/G]ccctccaaactgttt	79658
rs2043644	snp	C/T	0.451856	0.147493	intron-variant	ARHGAP10	GRCh38.p7	4:147819068	TGGGGCTCATTTGCA[C/T]AACTAATCTGATGTA	79658
rs2043645	snp	A/G	0.379942	0.213577	intron-variant	ARHGAP10	GRCh38.p7	4:147881071	ggccaggccagtctc[A/G]aactcctgacctcaa	79658
rs2055551	snp	A/G	0.439502	0.163061	intron-variant	ARHGAP10	GRCh38.p7	4:147771018	gtgggccctaatcca[A/G]tattactggtctcct	79658
rs2076947	snp	C/T	0.370365	0.219117	intron-variant	ARHGAP10	GRCh38.p7	4:148067008	CAGGACTTTGCTGGC[C/T]GGGGCACCCCGGGTG	79658
rs2118032	snp	A/G	0.0799831	0.183287	intron-variant	ARHGAP10	GRCh38.p7	4:147937138	taTTCAGCAGCCCCC[A/G]tccccaacctttttg	79658
rs2118033	snp	A/C	0.465052	0.127485	intron-variant	ARHGAP10	GRCh38.p7	4:147936949	tcctataacaatcta[A/C]tgtcgccactgatct	79658
rs2118034	snp	C/T	0.141258	0.225111	intron-variant	ARHGAP10	GRCh38.p7	4:147869497	TATTAAGGATTCCAA[C/T]CAGGTCATTTTGTGA	79658
rs2118035	snp	G/T	0.3746	0.216737	intron-variant	ARHGAP10	GRCh38.p7	4:147929976	ACATTTCATCATTAA[G/T]GAGGCACATGTGCAT	79658
rs2118036	snp	A/G	0.429688	0.173817	intron-variant	ARHGAP10	GRCh38.p7	4:147795339	TACCTTTTATCCTAC[A/G]TTTGTCTTTTTATAC	79658
rs2134706	snp	A/G	0.428484	0.175052	intron-variant	ARHGAP10	GRCh38.p7	4:147787353	GGGAGGAGTATTTTC[A/G]GTTTAGGAAACACAT	79658
rs2134707	snp	C/G	0.25801	0.249872	intron-variant	ARHGAP10	GRCh38.p7	4:147798308	GTTACTTATACAACA[C/G]CTGCTATTATTATTT	79658
rs2164527	snp	A/G	0.45866	0.137698	intron-variant	ARHGAP10	GRCh38.p7	4:147772079	TTTAGGGCCTGGCGC[A/G]GTTGCTCACGCCTGT	79658
rs2164528	snp	A/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147937282	gtacagagggggacc[A/G]tgagaagacacaggg	79658
rs2164529	snp	C/T	0.0799831	0.183287	intron-variant	ARHGAP10	GRCh38.p7	4:147936856	gttcctaataggcca[C/T]ggtctggggattggg	79658
rs2164530	snp	C/T	0.317451	0.240729	intron-variant	ARHGAP10	GRCh38.p7	4:147930045	TGTTGACAACAGGGG[C/T]AAAAGGTCATTAATG	79658
rs2164531	snp	C/T	0.317451	0.240729	intron-variant	ARHGAP10	GRCh38.p7	4:147929816	ATTATTTTAGATGCC[C/T]TATATGTATATATTT	79658
rs2174220	snp	C/T	0.16028	0.233346	intron-variant	ARHGAP10	GRCh38.p7	4:147798436	ATAATTTTGgccagg[C/T]gtggtggctcatgcc	79658
rs2262881	snp	A/G	0.395818	0.203069	intron-variant	ARHGAP10	GRCh38.p7	4:147952387	ccaacaatatacaaa[A/G]gttccatttcctttt	79658
rs2262882	snp	C/G	0.0244538	0.107838	intron-variant	ARHGAP10	GRCh38.p7	4:147952451	ttcattttagccatc[C/G]taataggtatttggt	79658
rs2276932	snp	C/T	0.110833	0.207684	missense, intron-variant, nc-transcript-variant	ARHGAP10	GRCh38.p7	4:148063170	TAAGCCACTGGACCA[C/T]AGACGATCGGGTCTG	79658
rs2306909	snp	C/T	0.208474	0.246527	intron-variant	ARHGAP10	GRCh38.p7	4:147965520	TTATAGATTTCATTC[C/T]CTTTTCCTCCTCCTT	79658
rs2306910	snp	C/T	0.334871	0.235153	intron-variant	ARHGAP10	GRCh38.p7	4:147965544	CCTCCTTTTAAAAAC[C/T]GGCAAAATCAAATCA	79658
rs2358097	snp	A/C	0.226188	0.248863	intron-variant	ARHGAP10	GRCh38.p7	4:147736793	GTCCGTTATGATAAA[A/C]CCATTTTCTGGGTTG	79658
rs2358176	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147904559	cctacaaggacatga[A/G]ctcatcattttttat	79658
rs2358177	snp	G/T			intron-variant	ARHGAP10	GRCh38.p7	4:147904568	acatgagctcatcat[G/T]ttttatggctgcata	79658
rs2358178	snp	A/C			intron-variant	ARHGAP10	GRCh38.p7	4:147904609	atgtatatgtgccac[A/C]ttttcttaatccaat	79658
rs2358179	snp	C/T	0.302184	0.244493	intron-variant	ARHGAP10	GRCh38.p7	4:147890496	taacaatgaaatggt[C/T]aaaagacctgaattt	79658
rs2358180	snp	A/T	0.324382	0.238678	intron-variant	ARHGAP10	GRCh38.p7	4:147924984	CTATTTTTTTTTTTT[A/T]AAAATAGCAATTTAC	79658
rs2358181	snp	A/G	0.441841	0.160303	intron-variant	ARHGAP10	GRCh38.p7	4:147939405	TTTCTATGGTTTTCA[A/G]AAATCATCCAAACAA	79658
rs2358182	snp	C/T	0.499382	0.017561	intron-variant	ARHGAP10	GRCh38.p7	4:148057255	TGGCAGAGTCTTAGG[C/T]ATTTGTAATTTGCAT	79658
rs2358183	snp	C/T	0.395453	0.203331	intron-variant	ARHGAP10	GRCh38.p7	4:148064711	GAATGCCACTATGCT[C/T]GCTTCTTGATTACTC	79658
rs2358184	snp	A/G	0.420415	0.182917	intron-variant	ARHGAP10	GRCh38.p7	4:148064755	ATCTTGTGGGTCTTC[A/G]TTCAGGTCATCTCTC	79658
rs2575581	snp	C/T	0.16846	0.236329			GRCh38.p7	4:147957040	TGATGATCTTGTCTG[C/T]GTTTCTGCAATCGTT	79658
rs2575582	snp	C/T	0.295854	0.245759			GRCh38.p7	4:147954151	aacacacattcccag[C/T]gcatacaggccattt	79658
rs2575583	snp	A/G	0	0			GRCh38.p7	4:147953025	ATGATCATATCAATa[A/G]acaatttaggagaaa	79658
rs2575584	snp	C/G	0.487995	0.0765403			GRCh38.p7	4:147951658	taagaccagcctagg[C/G]aacaaagtgagaccc	79658
rs2575585	snp	C/T	0.286303	0.24735			GRCh38.p7	4:147950942	AAATCATAATATTTA[C/T]CTAAGCTGGCATTTC	79658
rs2575588	snp	C/T					GRCh38.p7	4:147938027	cgttcctttttaggg[C/T]tgcatagtagtccgt	79658
rs2575591	snp	A/G	0.0984431	0.198823			GRCh38.p7	4:147936369	tgcagtccgcagtcc[A/G]gcctgggcgacagag	79658
rs2575594	snp	A/T					GRCh38.p7	4:147773300	GAGCTTTATAGTAAG[A/T]TCACCCAGTTCATCA	79658
rs2575595	snp	A/G	0	0			GRCh38.p7	4:147785881	CTTTATCCTTTAGAT[A/G]GGCAAACCACTCCCT	79658
rs2575596	snp	C/G					GRCh38.p7	4:147785902	ACCACTCCCTATTTT[C/G]ATAATTTGTCACCAA	79658
rs2575597	snp	A/G					GRCh38.p7	4:147912877	agtcaggaactccca[A/G]actcaagtgatcatt	79658
rs2575598	snp	G/T					GRCh38.p7	4:147912912	ctgggcctcccaaag[G/T]ggggggattacaggt	79658
rs2575599	snp	G/T					GRCh38.p7	4:147912915	ggcctcccaaagggg[G/T]gggattacaggtgtg	79658
rs2575601	snp	G/T					GRCh38.p7	4:147787550	GGCAGGAGAGGTGGT[G/T]GGATTTGGGAAAACT	79658
rs2635255	snp	A/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147937411	tccaaatgtgactgt[A/G]tttagaaataaggtc	79658
rs2635256	snp	G/T	0.456803	0.140473	intron-variant	ARHGAP10	GRCh38.p7	4:147935802	AGCAGCTTGGAAATC[G/T]CACGTAAAATACATA	79658
rs2635257	snp	C/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147927689	TCACCCTGTTTCTGC[C/T]GCCATAGGATAAGTC	79658
rs2635259	snp	C/T	0.383053	0.211653	intron-variant	ARHGAP10	GRCh38.p7	4:147953200	GACCAATATCACTCA[C/T]GAACATAGATGCAAC	79658
rs2635260	snp	A/C	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147953187	cacgaacatagatgc[A/C]actattctaaataaa	79658
rs2635261	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147953176	atgcaactattctaa[A/G]taaaatgttactaaa	79658
rs2635262	snp	A/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147953147	aatcaaattccacaa[A/G]ataaataaaataata	79658
rs2635263	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147952688	tcacagaatgaagaa[A/G]atacttgtaaagcag	79658
rs2635264	snp	C/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147951473	TGAAAAAGTCCTGCT[C/T]TTATTTCCCCTCCCT	79658
rs2635265	snp	A/G	0.123452	0.215605	intron-variant	ARHGAP10	GRCh38.p7	4:147949260	CTCATCTAAACCACA[A/G]TTAGTCACTATCAGT	79658
rs2635266	snp	C/T	0.438806	0.163867	intron-variant	ARHGAP10	GRCh38.p7	4:147945375	AGTCAGTTAATAGGG[C/T]TGCTTCTTTATAAAG	79658
rs2635267	snp	G/T	0.405429	0.195811	intron-variant	ARHGAP10	GRCh38.p7	4:147944581	AACCTGTCAAAATGG[G/T]ACCACCACATTAAGT	79658
rs2635268	snp	C/T	0.440057	0.162414	intron-variant	ARHGAP10	GRCh38.p7	4:147940686	GCACACCTGAGGGCA[C/T]TGTTAATATTGATTA	79658
rs2635269	snp	C/G	0.12932	0.218944	intron-variant	ARHGAP10	GRCh38.p7	4:147914420	cagtgagctatggct[C/G]caccaccacactcca	79658
rs2635270	snp	A/C	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147912836	acatggtgaggcccc[A/C]cctctactgaagatg	79658
rs2654932	snp	A/C	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147773173	GAAGGGAAATCTGCT[A/C]TTTTTAAATATTTTC	79658
rs2654933	snp	A/T			intron-variant	ARHGAP10	GRCh38.p7	4:147787554	GGAGAGGTGGTTGGA[A/T]TTGGGAAAACTAATC	79658
rs2654934	snp	C/T			intron-variant	ARHGAP10	GRCh38.p7	4:147787663	TCTGAGCCCACTGCC[C/T]TCGTGCTTCCCTGGC	79658
rs2654954	snp	C/T	0.5	0	intron-variant	ARHGAP10	GRCh38.p7	4:147783700	AAATTATACAATACA[C/T]AATTTAATGTGTTCT	79658
rs2654955	snp	C/T	0.375	0.216506	intron-variant	ARHGAP10	GRCh38.p7	4:147783568	AAATTATACAATACA[C/T]AATTTAATGTGTGTT	79658
rs2654956	snp	C/T	0.375	0.216506	intron-variant	ARHGAP10	GRCh38.p7	4:147783519	ATAATTTAATGTGTG[C/T]TCTATAAATTATACA	79658
rs2654957	snp	A/C	0.375	0.216506	intron-variant	ARHGAP10	GRCh38.p7	4:147783517	AATTTAATGTGTGTT[A/C]TATAAATTATACAAT	79658
rs2654958	snp	A/C	0	0	intron-variant, upstream-variant-2KB	ARHGAP10, MIR4799	GRCh38.p7	4:147781622	GTGAAACACTTAGCC[A/C]TTAACGATATTCTTA	79658
rs2884400	snp	A/G	0.450231	0.149691	intron-variant	ARHGAP10	GRCh38.p7	4:147885152	ACAAAGTGGGGGCAT[A/G]AGGATGGGGGAAGAC	79658
rs2884401	snp	C/G	0.4231	0.180378	intron-variant	ARHGAP10	GRCh38.p7	4:148062931	ACCTGGAGAAGGACA[C/G]TAAGACAGCTTGAGT	79658
rs3037174	in-del	-/A/AAA/AAAA	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147785100	AAAAAAAAAAAAAAA[-/A/AAA/AAAA]GAATAACATCTAAGC	79658
rs3039229	in-del	-/TTGA	0.450357	0.149522	intron-variant	ARHGAP10	GRCh38.p7	4:147890294	CTAGCCATTACTACT[-/TTGA]TTATCAATGGTTAGA	79658
rs3221517	microsatellite	(CA)17/19/20/21/22	0.443474	0.290326	intron-variant	ARHGAP10	GRCh38.p7	4:147870007	aacaaataaatgaaa[(CA)17/19/20/21/22]aaaaaaaaaCTGGGA	79658
rs3221738	microsatellite	(CA)24/25/28/32/33/34	0.26208	0.287954	intron-variant	ARHGAP10	GRCh38.p7	4:147741769	ATATCGTTCTCTTTA[(CA)24/25/28/32/33/34]CAGGCGCTTTGCATT	79658
rs3775327	snp	A/G	0.40733	0.194287	intron-variant	ARHGAP10	GRCh38.p7	4:148064569	CTGACTGCTCACTCC[A/G]TGCTGCAGACTTATT	79658
rs3857094	snp	C/T	0.0352966	0.128072	intron-variant	ARHGAP10	GRCh38.p7	4:147900132	ATGGTTTGATAGAGC[C/T]ATAGAACATGCAGTT	79658
rs3857095	snp	A/C	0.199873	0.244923	intron-variant	ARHGAP10	GRCh38.p7	4:147901632	CTACTTTACTTTTTA[A/C]GCTTCTTTGGATTTT	79658
rs3884525	snp	C/G	0.405255	0.195948	intron-variant	ARHGAP10	GRCh38.p7	4:148070363	AGCTTCTGGCTTCAA[C/G]GCCTCCCTGGAGCTG	79658
rs3893175	snp	A/G	0.4444	0.15719	intron-variant	ARHGAP10	GRCh38.p7	4:147900469	ATAAATTTCATGAAC[A/G]AAAAAAATAAACCAA	79658
rs3951256	snp	A/C/T	0.000399281	0.0141238	intron-variant	ARHGAP10	GRCh38.p7	4:147904388	ccctcccccgtcccc[A/C/T]caccccacaacaatc	79658
rs3990920	snp	A/T	0.46703	0.124089	intron-variant	ARHGAP10	GRCh38.p7	4:147899985	TGTAAACAGAGTAGC[A/T]CTTAAGTGAATAAAC	79658
rs4027114	snp	A/G	0.310386	0.242597	intron-variant	ARHGAP10	GRCh38.p7	4:147918559	TTTAGTATGACTACT[A/G]GAAAATGTATAATTG	79658
rs4027115	snp	A/G	0.292266	0.246401	intron-variant	ARHGAP10	GRCh38.p7	4:147918566	TGACTACTGGAAAAT[A/G]TATAATTGCATAGGT	79658
rs4027136	in-del	-/AT			intron-variant	ARHGAP10	GRCh38.p7	4:147784837	ATATTATAAATATAT[-/AT]TATAAAATATATATT	79658
rs4240338	snp	C/T	0.290201	0.246747	intron-variant	ARHGAP10	GRCh38.p7	4:147820957	TCTTTTCAATTACCC[C/T]CAAACCTAATGGCTA	79658
rs4240339	snp	A/G	0.224412	0.248687	intron-variant	ARHGAP10	GRCh38.p7	4:147821163	GCTTGTTCTCGTGAA[A/G]GACTGAGGGTTCCAT	79658
rs4240340	snp	C/T	0.214239	0.247429	intron-variant	ARHGAP10	GRCh38.p7	4:147856435	TATTGCTATAcaggt[C/T]gatcatcctgaatct	79658
rs4240341	snp	A/G	0.430136	0.173352	intron-variant	ARHGAP10	GRCh38.p7	4:147866518	ATTTAAGGGAAAAAA[A/G]CATCATTTTCTATAA	79658
rs4240342	snp	A/G	0.142272	0.225598	intron-variant	ARHGAP10	GRCh38.p7	4:147874357	TGTATATATGTTTTC[A/G]GTGTAGCCGTTTGAC	79658
rs4240343	snp	A/G	0.304438	0.244001	intron-variant	ARHGAP10	GRCh38.p7	4:147911547	TATTGTATTTTTAGT[A/G]GAGACGGGGTTTCAC	79658
rs4240344	snp	C/T	0.413416	0.189196	intron-variant	ARHGAP10	GRCh38.p7	4:147911583	TAGCCAGGATGGTCT[C/T]GATCTCCTGACTTCG	79658
rs4240345	snp	C/G	0.159292	0.232964	intron-variant	ARHGAP10	GRCh38.p7	4:147918290	ACAGGTGCCCGCCAC[C/G]AAGCCTGGCTAATTT	79658
rs4240346	snp	C/G	0.122758	0.215196	intron-variant	ARHGAP10	GRCh38.p7	4:147948849	tgggcgcctgtagtc[C/G]cagctactcgggagg	79658
rs4292310	snp	A/G	0.218151	0.247963	intron-variant	ARHGAP10	GRCh38.p7	4:147826313	GTTGTTAGCCAACTG[A/G]CTGGTTTAAGCTCCA	79658
rs4293769	snp	A/G	0.378372	0.214524	intron-variant	ARHGAP10	GRCh38.p7	4:148003442	aggtccacttggtgc[A/G]gagctgagtttaatt	79658
rs4333167	snp	A/G	0.333722	0.235565	intron-variant	ARHGAP10	GRCh38.p7	4:147999469	tgccattgcagcccc[A/G]ccactgacttccatc	79658
rs4337713	snp	A/G	0.309894	0.242719	intron-variant	ARHGAP10	GRCh38.p7	4:147926941	GTGTTATTTTCTCAT[A/G]AGAACCATGTGAGAC	79658
rs4364238	snp	C/T	0.259397	0.249823	intron-variant	ARHGAP10	GRCh38.p7	4:148003453	gtgcggagctgagtt[C/T]aattcctggatatcc	79658
rs4379049	snp	C/T	0.188946	0.24243	intron-variant	ARHGAP10	GRCh38.p7	4:147736621	TTCCCCTCTGACAAT[C/T]CAGATTTCATTCAAG	79658
rs4393981	snp	C/G	0.0941369	0.195465	intron-variant	ARHGAP10	GRCh38.p7	4:147985882	AGGGAAATGACAGCG[C/G]GAGGTCCTCTGCCTC	79658
rs4419463	snp	C/T	0.290977	0.246619	intron-variant	ARHGAP10	GRCh38.p7	4:147818454	GCCTGTAATTCCAGC[C/T]ACTTGGGAGGCTGAG	79658
rs4429719	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147784761	TATATATTATAAAAT[A/G]TATATTATAAATATA	79658
rs4463051	snp	A/G	0.0194378	0.0966492	missense, nc-transcript-variant	ARHGAP10	GRCh38.p7	4:147866772	CATGAACTTGCCAAA[A/G]ACTTCAATCACTACA	79658
rs4490438	snp	C/T	0.248471	0.249995	intron-variant	ARHGAP10	GRCh38.p7	4:147740011	aaagtcctgggatta[C/T]aggtgtgagccactg	79658
rs4491995	snp	C/T	0.273856	0.248859	intron-variant	ARHGAP10	GRCh38.p7	4:147903309	TTTCTGAGAGACTAC[C/T]TTTTAAAGAATAGTT	79658
rs4496566	snp	A/G	0.228547	0.249078	intron-variant	ARHGAP10	GRCh38.p7	4:147734924	TATTTTACAAAAATG[A/G]CCTTTTGAGCATTTC	79658
rs4527453	snp	A/G	0.179744	0.239925	intron-variant	ARHGAP10	GRCh38.p7	4:147934206	TTCAACTGCAGGCTC[A/G]AGGCCAAAGAGGGCT	79658
rs4527458	snp	G/T	0.230017	0.2492	intron-variant	ARHGAP10	GRCh38.p7	4:147903364	gatagagattttcct[G/T]attccccccaactcc	79658
rs4529033	snp	A/G	0.162909	0.23434	intron-variant	ARHGAP10	GRCh38.p7	4:147903319	actactttttaaaga[A/G]tagttttcagttcac	79658
rs4571312	snp	C/T	0.40386	0.197046	intron-variant	ARHGAP10	GRCh38.p7	4:147895866	ttatttaaagtgtaa[C/T]attagctgaaaattg	79658
rs4594709	snp	C/T	0.170084	0.236883	intron-variant	ARHGAP10	GRCh38.p7	4:147930305	GTTGTTGTATCTTTT[C/T]CTGTCATGTATTTTA	79658
rs4596224	snp	A/T	0.5	0	intron-variant	ARHGAP10	GRCh38.p7	4:147811590	TGCAATGGCTTTTTT[A/T]AAAAAAAAAAAACAA	79658
rs4605627	snp	A/G	0.0111196	0.0737302	intron-variant	ARHGAP10	GRCh38.p7	4:147943659	ATTTTTAACAAACCC[A/G]TAAAGTGTCCTTCCT	79658
rs4618299	snp	C/T			intron-variant	ARHGAP10	GRCh38.p7	4:147897217	AAAATATGCTAGCCA[C/T]TGCTTTTTAAGCAGA	79658
rs4626180	snp	A/G	0.0425829	0.139564	intron-variant	ARHGAP10	GRCh38.p7	4:147946166	TGGGGACTCTACCCT[A/G]CTTAGTTGGCTGTCT	79658
rs4627844	snp	A/G	0.475525	0.107882	intron-variant	ARHGAP10	GRCh38.p7	4:147909919	ACGTAATAATCCTCT[A/G]TTGCATGTGTTCTGT	79658
rs4835093	snp	A/G	0.431177	0.172264	intron-variant	ARHGAP10	GRCh38.p7	4:147734125	CTTGATGTTAACCAG[A/G]GTCAGTGGCCGGGAG	79658
rs4835094	snp	C/T	0.00358779	0.0422022	intron-variant	ARHGAP10	GRCh38.p7	4:147748881	GGAGGATTGCTTGAA[C/T]CCGGGAGATTGATGC	79658
rs4835101	snp	C/T	0.453209	0.145623	intron-variant	ARHGAP10	GRCh38.p7	4:147850019	AAACGCACCAATCAG[C/T]GCTCTGTATCTAGCC	79658
rs4835102	snp	C/T	0.153	0.230415	intron-variant	ARHGAP10	GRCh38.p7	4:147860495	GAAAATTGTGGCATA[C/T]ACCATGCTGGCTATT	79658
rs4835103	snp	A/G	0.446902	0.154045	intron-variant	ARHGAP10	GRCh38.p7	4:147874706	TTAAACCTAAAATTT[A/G]GTAATAGTGTGAGAC	79658
rs4835104	snp	A/T	0.147321	0.227941	intron-variant	ARHGAP10	GRCh38.p7	4:147886305	ctttcagcacttggc[A/T]tcttgacttgttaag	79658
rs4835105	snp	A/G	0.145642	0.227177	intron-variant	ARHGAP10	GRCh38.p7	4:147891214	tataatagccaaaaa[A/G]tagaaacaacctaaa	79658
rs4835106	snp	G/T	0.20111	0.245173	intron-variant	ARHGAP10	GRCh38.p7	4:147901185	TAAGCAATTGATTAT[G/T]AGAAAAGAAAAACTT	79658
rs4835107	snp	C/T	0.142947	0.22592	intron-variant	ARHGAP10	GRCh38.p7	4:147902911	gaagagagagagaag[C/T]gggaggggagggcgg	79658
rs4835108	snp	A/G	0.146314	0.227484	intron-variant	ARHGAP10	GRCh38.p7	4:147906037	tggctctctttgtct[A/G]ttatttgtgtataag	79658
rs4835109	snp	A/G	0.429087	0.174436	intron-variant	ARHGAP10	GRCh38.p7	4:147906216	tgaaagcaggggcct[A/G]aacaggtatttgtac	79658
rs4835110	snp	A/G	0.429238	0.174281	intron-variant	ARHGAP10	GRCh38.p7	4:147906257	ATAGCAGCACTGTTC[A/G]CAACAGGCAAAAAGG	79658
rs4835111	snp	G/T	0.212425	0.24716	intron-variant	ARHGAP10	GRCh38.p7	4:147927132	ACTATAGTCTGACCT[G/T]TTTTTGAGGATGTTG	79658
rs4835121	snp	G/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:148001316	gttttggttactgta[G/T]ccttgtagtatagtt	79658
rs4835123	snp	A/C	0.175254	0.238565	intron-variant	ARHGAP10	GRCh38.p7	4:148009339	GTTTCACCATGTTGG[A/C]CAGTCTGGTCTCCAA	79658
rs4835450	snp	A/T	0.00159617	0.0282053	intron-variant	ARHGAP10	GRCh38.p7	4:147741232	AGCCTTATTGAAATT[A/T]GTTTTATAAATTTAG	79658
rs4835456	snp	A/T	0.433963	0.169285	intron-variant	ARHGAP10	GRCh38.p7	4:147809490	CCTTCACTGCAATTC[A/T]ACATGTAAACTCCAA	79658
rs4835457	snp	G/T	0.434398	0.168811	intron-variant	ARHGAP10	GRCh38.p7	4:147812613	GCTTCTTTCTTCTCT[G/T]CTAATATTTCAACAT	79658
rs4835458	snp	A/G	0.0766824	0.180169	intron-variant	ARHGAP10	GRCh38.p7	4:147815993	gttactacagcaata[A/G]gaaatgaatacGTAA	79658
rs4835459	snp	C/T	0.21695	0.247806	intron-variant	ARHGAP10	GRCh38.p7	4:147825810	TTGATAGTTGTACTT[C/T]CCTGGCATCCTGAAC	79658
rs4835461	snp	G/T	0.440884	0.161442	intron-variant	ARHGAP10	GRCh38.p7	4:147834565	TAATGCCAGACTGGG[G/T]ATTAAGTTTCAACTT	79658
rs4835462	snp	A/T	0.178785	0.239642	intron-variant	ARHGAP10	GRCh38.p7	4:147835792	TCTCTTATGTAAAAC[A/T]AAAAAAAAATTCAAA	79658
rs4835463	snp	C/T	0.422158	0.181278	intron-variant	ARHGAP10	GRCh38.p7	4:147850512	agacaactctctatg[C/T]gccacctttaagagc	79658
rs4835464	snp	C/T	0.413914	0.188765	intron-variant	ARHGAP10	GRCh38.p7	4:147860320	GGTGGCAGGTGCCTG[C/T]AGTCCCAGCTACTCA	79658
rs4835465	snp	C/T	0.136166	0.22258	intron-variant	ARHGAP10	GRCh38.p7	4:147864360	CTGGCTCCTTCTCAC[C/T]TGCCGCCATCACTCC	79658
rs4835466	snp	C/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147866124	AAGATTTCCTTAACT[C/G]TCTCCCCAGATCACT	79658
rs4835467	snp	G/T	0.146985	0.227789	intron-variant	ARHGAP10	GRCh38.p7	4:147883665	gcccctgcattctcc[G/T]cctagagcccCACAT	79658
rs4835468	snp	C/G	0.429087	0.174436	intron-variant	ARHGAP10	GRCh38.p7	4:147905897	atttgtttgtattct[C/G]ttttctttcattgag	79658
rs4835469	snp	C/T	0.478188	0.10213	intron-variant	ARHGAP10	GRCh38.p7	4:147911099	TTCTTATTGCAGAGA[C/T]GTTAAAACATGTCTT	79658
rs4835475	snp	C/T	0.373598	0.21731	intron-variant	ARHGAP10	GRCh38.p7	4:148001218	ttgtcaaagatcata[C/T]ggttgtagatgtgtg	79658
rs4835477	snp	C/T	0.0310518	0.120672	intron-variant	ARHGAP10	GRCh38.p7	4:148052079	TACACCACAGTAAAC[C/T]GTGAATGATTTGCCT	79658
rs5010609	snp	A/T	0.0142736	0.0832652	intron-variant	ARHGAP10	GRCh38.p7	4:147924983	TCTATTTTTTTTTTT[A/T]TAAAATAGCAATTTA	79658
rs5862810	in-del	-/T			intron-variant	ARHGAP10	GRCh38.p7	4:147737343	TTTTTTTTTTTTTTT[-/T]GTAAAGACAGGGTTT	79658
rs5862811	in-del	-/C/G	0.5	0	intron-variant	ARHGAP10	GRCh38.p7	4:147787451	TGGAGTGATGGAAGC[-/C/G]GGTGGGGGAGGAGGC	79658
rs5862812	in-del	-/T	0.301932	0.244547	intron-variant	ARHGAP10	GRCh38.p7	4:147798149	CAGTTTTGCTTTTAC[-/T]TTTTTTTTTTTCGTA	79658
rs5862813	in-del	-/A			intron-variant	ARHGAP10	GRCh38.p7	4:147818585	AAAAAAAAAAAAAAA[-/A]GTTAGTTTGTTAGTT	79658
rs5862814	in-del	-/T	0.142272	0.225598	intron-variant	ARHGAP10	GRCh38.p7	4:147877265	AATATCTGTGCAATA[-/T]TTTTTTTGTCAACCA	79658
rs5862815	in-del	-/A	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147880916	TTTACACTAAAAAAA[-/A]GAGTACAATAAGAGA	79658
rs5862816	in-del	-/A	0.413914	0.188765	intron-variant	ARHGAP10	GRCh38.p7	4:147899722	TTTTATCATCTCTGG[-/A]AAAAAATGCATGATT	79658
rs5862818	in-del	-/T	0.428182	0.17536	intron-variant	ARHGAP10	GRCh38.p7	4:147899877	TTGTTACGTGCTGGG[-/T]TTTTTTTTTTTTTTC	79658
rs5862820	in-del	-/G	0.319136	0.24025	intron-variant	ARHGAP10	GRCh38.p7	4:147911643	TGGGATTACAGGCGT[-/G]GAGCCACCGCGCCTG	79658
rs5862821	in-del	-/C			intron-variant	ARHGAP10	GRCh38.p7	4:147911647	TTACAGGCGTGGAGC[-/C]ACCGCGCCTGGCCTC	79658
rs5862822	in-del	-/A	0.447032	0.153878	intron-variant	ARHGAP10	GRCh38.p7	4:147920641	CAACGTTGGTTACAT[-/A]ACAATCCTTGATTTA	79658
rs5862823	in-del	-/A	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147924747	CTTATTAACTCTGCC[-/A]TGTAACCTCTCTGTG	79658
rs5862824	in-del	-/A			intron-variant	ARHGAP10	GRCh38.p7	4:147931314	AATTTATTAAGAGAG[-/A]AAAAAAAAAAAAACT	79658
rs5862825	in-del	-/T	0.438105	0.164671	intron-variant	ARHGAP10	GRCh38.p7	4:147949842	CAATAAATTGCATTC[-/T]TTTTTTCCTCCATTC	79658
rs6535556	snp	A/G	0.448323	0.15221	intron-variant	ARHGAP10	GRCh38.p7	4:147744055	AGAAACGTGTATATT[A/G]GTGCAGAAGAGTTCT	79658
rs6535557	snp	A/G	0.00358779	0.0422022	intron-variant	ARHGAP10	GRCh38.p7	4:147744800	caggagacatgttca[A/G]tagtgtgtttctttt	79658
rs6535558	snp	C/T	0.434976	0.168179	intron-variant	ARHGAP10	GRCh38.p7	4:147763845	ctgcagcctcaactt[C/T]ctgggctcaggtgat	79658
rs6535559	snp	C/T	0.439502	0.163061	intron-variant	ARHGAP10	GRCh38.p7	4:147770271	ggtgccagtggttca[C/T]gcctgtctgtaatcc	79658
rs6535560	snp	A/G	0.440884	0.161442	intron-variant	ARHGAP10	GRCh38.p7	4:147770398	ggcatggtggtgggc[A/G]cctgtaatcccagct	79658
rs6535561	snp	C/T	0.435263	0.167862	intron-variant	ARHGAP10	GRCh38.p7	4:147773507	TGTTATGTTTTACAG[C/T]ATCTATTAGAAATCA	79658
rs6535562	snp	C/T	0.077417	0.180873	intron-variant	ARHGAP10	GRCh38.p7	4:147816539	AGTTAGGGCCAGGAA[C/T]GCTTTACCAGAATAG	79658
rs6535563	snp	C/T	0.150667	0.229419	intron-variant	ARHGAP10	GRCh38.p7	4:147816629	GGCCTAACCTAGCCC[C/T]GTGATGCATTCTGGG	79658
rs6535564	snp	A/G	0.158962	0.232835	intron-variant	ARHGAP10	GRCh38.p7	4:147857268	TGAGGGGTGAGTGAC[A/G]TGGAATTAATTTTTA	79658
rs6535565	snp	C/T	0.423413	0.180077	intron-variant	ARHGAP10	GRCh38.p7	4:147861058	ctggcccgctgggct[C/T]gttctgcctgctctt	79658
rs6535566	snp	C/G	0.174932	0.238463	intron-variant	ARHGAP10	GRCh38.p7	4:147861683	agtgtccagctctca[C/G]tggagaggagacctg	79658
rs6535567	snp	G/T	0.234401	0.249513	intron-variant	ARHGAP10	GRCh38.p7	4:147870000	AAAAAGTCCCAGTTT[G/T]TGTGTGTGTGTGTGT	79658
rs6535568	snp	A/C	0.00953873	0.0683987	intron-variant	ARHGAP10	GRCh38.p7	4:147874036	GTGTTTAAAAAAAAA[A/C]AACAAACCTCTGCAG	79658
rs6535569	snp	G/T	0.454423	0.143914	intron-variant	ARHGAP10	GRCh38.p7	4:147876511	GGCAGGAGAATGGCG[G/T]GAACCTGGGAGGCGG	79658
rs6535570	snp	C/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147887199	gctgtaacaagagct[C/G]tttcccgctctagac	79658
rs6535571	snp	C/T	0.270351	0.24917	intron-variant	ARHGAP10	GRCh38.p7	4:147992526	CATTCTCTTGTAGCC[C/T]TCCTGAGAGGCTGGG	79658
rs6535572	snp	A/G	0.270351	0.24917	intron-variant	ARHGAP10	GRCh38.p7	4:147992587	atttttgtattttta[A/G]tagagatggggtttc	79658
rs6535574	snp	A/C	0.36315	0.222928	intron-variant	ARHGAP10	GRCh38.p7	4:148007650	tgtctcccaagttaa[A/C]ctgctcaagcattgt	79658
rs6535576	snp	A/G	0.494936	0.050064	intron-variant	ARHGAP10	GRCh38.p7	4:148065653	TGGCTGAAGGGGAGG[A/G]TGCGATGGTAGTATT	79658
rs6810743	snp	C/T	0.00159617	0.0282053	intron-variant	ARHGAP10	GRCh38.p7	4:148004187	atagcatgaccctgt[C/T]tcaaaaataaaaaaT	79658
rs6810966	snp	C/T	0.00159617	0.0282053	intron-variant	ARHGAP10	GRCh38.p7	4:148001177	tgaatagggaatcct[C/T]tccccatttcctatt	79658
rs6811180	snp	A/T			intron-variant	ARHGAP10	GRCh38.p7	4:147798722	GGTCAGGAGTTTGAG[A/T]CActctctctctctc	79658
rs6811189	snp	A/T	0.246485	0.249975	intron-variant	ARHGAP10	GRCh38.p7	4:147798724	TCAGGAGTTTGAGAc[A/T]ctctctctctctctc	79658
rs6811234	snp	A/C			intron-variant	ARHGAP10	GRCh38.p7	4:147798783	tctctctctctctct[A/C]tatatatatatatat	79658
rs6811259	snp	A/G	0.259674	0.249813	intron-variant	ARHGAP10	GRCh38.p7	4:148004529	AGATTGTCTTAGACC[A/G]GAGAGAGAAATTCTC	79658
rs6811391	snp	A/C			intron-variant	ARHGAP10	GRCh38.p7	4:147798785	tctctctctctctat[A/C]tatatatatatatat	79658
rs6811430	snp	C/T	0.39325	0.204889	intron-variant	ARHGAP10	GRCh38.p7	4:148034596	GGCCTCCCAGAGTGC[C/T]GGGATTACAGGTGTG	79658
rs6811580	snp	C/T	0.338069	0.233974	intron-variant	ARHGAP10	GRCh38.p7	4:147798830	ataGACTTTTTACCC[C/T]CCCAcgcttgaaaaa	79658
rs6811769	snp	A/T	0.47852	0.101384	intron-variant	ARHGAP10	GRCh38.p7	4:147907690	GCAATCTTGAAGTAC[A/T]TGGAAAATGAAAACC	79658
rs6812152	snp	C/G			intron-variant	ARHGAP10	GRCh38.p7	4:147798950	gcctgctttcaagca[C/G]atttttttctttgtc	79658
rs6813344	snp	C/T	0.0414363	0.137845	intron-variant	ARHGAP10	GRCh38.p7	4:147992261	ATTTTTTGGAGAAGC[C/T]AGGTGTTGCCACGTT	79658
rs6813714	snp	A/G	0.0832709	0.186283	intron-variant	ARHGAP10	GRCh38.p7	4:147809302	TGACCTCTATCTGCA[A/G]CCGTTTGTGGAATTT	79658
rs6814079	snp	A/G	0.199564	0.24486	intron-variant	ARHGAP10	GRCh38.p7	4:147992429	ttaattttttttgtg[A/G]aggagtctcgctctg	79658
rs6814095	snp	A/G	0.195837	0.244062	intron-variant	ARHGAP10	GRCh38.p7	4:147992444	gaggagtctcgctct[A/G]ttgcccagcgtggag	79658
rs6814346	snp	C/T	0.200801	0.245111	intron-variant	ARHGAP10	GRCh38.p7	4:147992705	gccattgcaccTGGC[C/T]GAAAAAGCCTTTTAA	79658
rs6815554	snp	A/C	0.203267	0.245593	intron-variant	ARHGAP10	GRCh38.p7	4:148017447	GACAGTACCTGATAC[A/C]CCCTCACTTGTATCA	79658
rs6815620	snp	C/T	0.0554779	0.157039	intron-variant	ARHGAP10	GRCh38.p7	4:147943357	ATTACCTTGTTTCCT[C/T]TGTAGGACAGCTTTG	79658
rs6817545	snp	C/T	0.457969	0.138741	intron-variant	ARHGAP10	GRCh38.p7	4:148056238	CTTAAAACCCAGCTT[C/T]AGGAAGTGCAGTTAA	79658
rs6818043	snp	C/T	0.221141	0.248329	intron-variant	ARHGAP10	GRCh38.p7	4:147762299	aggtgggagccactg[C/T]gtcctgccCAGAAAT	79658
rs6818130	snp	A/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147852731	ttttttttttttttt[A/T]aaatggagcggagtt	79658
rs6818371	snp	C/T	0.380529	0.213219	intron-variant	ARHGAP10	GRCh38.p7	4:147878521	AGCACTATGATTCTA[C/T]AATTCTATCATTTTG	79658
rs6820696	snp	C/G	0.161267	0.233723	intron-variant	ARHGAP10	GRCh38.p7	4:147935609	GCTGGAAAAGGACAT[C/G]ATAAACTCACTAATA	79658
rs6822971	snp	C/T	0.434253	0.168969	intron-variant	ARHGAP10	GRCh38.p7	4:147766488	tcaaattgttttgat[C/T]gcagtcagttgaatc	79658
rs6823034	snp	A/G	0.00119737	0.0244387	intron-variant	ARHGAP10	GRCh38.p7	4:147748094	AAACTCTGCCTTAGA[A/G]ATAGGGAGCCCATGT	79658
rs6824449	snp	A/G	0.484209	0.0874434	intron-variant	ARHGAP10	GRCh38.p7	4:148069844	GTTACAACCCTGAGG[A/G]CCTGTTTTGCATAGA	79658
rs6824823	snp	A/T	0.252983	0.249982	intron-variant	ARHGAP10	GRCh38.p7	4:147814427	GTGCCGTGAATGTTG[A/T]TACTCCAATGGCAGA	79658
rs6826041	snp	A/G	0.376989	0.215346	intron-variant	ARHGAP10	GRCh38.p7	4:147999972	agggtacatgtgcac[A/G]acgtgcgggtttgtt	79658
rs6827412	snp	A/G	0.456214	0.141336	intron-variant	ARHGAP10	GRCh38.p7	4:148054484	TCCTCTGAGAATGTA[A/G]TTTAATATTCTTAGT	79658
rs6828600	snp	A/G	0.307176	0.243374	intron-variant	ARHGAP10	GRCh38.p7	4:147748486	tattgtatacttaca[A/G]ttttcctaagagggt	79658
rs6829479	snp	A/G	0.439502	0.163061	intron-variant	ARHGAP10	GRCh38.p7	4:147799428	tattcttttagccct[A/G]ttctctttttcctct	79658
rs6830938	snp	A/G	0.00279162	0.0372561	intron-variant	ARHGAP10	GRCh38.p7	4:147983064	ttttgcattttttgt[A/G]gagatgggggtctca	79658
rs6832527	snp	C/T	0.345925	0.230864	intron-variant	ARHGAP10	GRCh38.p7	4:147873546	AGATGGGGATAAGgg[C/T]gggggatggtggctc	79658
rs6836509	snp	C/T	0.459118	0.137002	intron-variant	ARHGAP10	GRCh38.p7	4:147733500	TGGGTTCTTAGGGCC[C/T]TCATCACTCACCTAG	79658
rs6837391	snp	A/G	0.429987	0.173507	intron-variant	ARHGAP10	GRCh38.p7	4:147800932	ttcttgtgcctccca[A/G]gtagctgggactaca	79658
rs6838520	snp	A/T	0.0119091	0.0762411	intron-variant	ARHGAP10	GRCh38.p7	4:147758671	TGGTGtatttttttt[A/T]aatttattattatta	79658
rs6838916	snp	A/C	0.410061	0.192043	intron-variant	ARHGAP10	GRCh38.p7	4:148008610	ctgagattgagaagc[A/C]GTCAGCAGATTAATG	79658
rs6839164	snp	A/G	0.00199481	0.0315187	intron-variant	ARHGAP10	GRCh38.p7	4:148001346	ttgaagtcaggtagc[A/G]tgatgcctccagctt	79658
rs6839440	snp	A/G	0.381503	0.21262	intron-variant	ARHGAP10	GRCh38.p7	4:147856175	TTAGGGGAGACACCC[A/G]TCTTCTCTGCATTTA	79658
rs6839459	snp	A/G	0.228253	0.249052	intron-variant	ARHGAP10	GRCh38.p7	4:148031831	CCCTCCAGGAGAAAA[A/G]TCCAGGCCTGTTTTT	79658
rs6839547	snp	A/G	0.0383715	0.133092	intron-variant	ARHGAP10	GRCh38.p7	4:148008991	ttatgttaatatgtA[A/G]TGGTTTAGtattaaa	79658
rs6839648	snp	A/G	0.0482946	0.147699	intron-variant	ARHGAP10	GRCh38.p7	4:148008831	gtgttttccagaggc[A/G]atgatattaagacat	79658
rs6839987	snp	C/T	0.434253	0.168969	intron-variant	ARHGAP10	GRCh38.p7	4:147766052	ttggtagtctgaggc[C/T]ggtggatcacttgag	79658
rs6840039	snp	A/G	0.434253	0.168969	intron-variant	ARHGAP10	GRCh38.p7	4:147766183	tagtcccagctactc[A/G]ggagcctgaggcagg	79658
rs6840771	snp	A/G	0.37138	0.218556	intron-variant	ARHGAP10	GRCh38.p7	4:147878462	ACTAGGATGCTGTTC[A/G]TGGACTTAAAGCACT	79658
rs6841530	snp	C/T	0.277067	0.24853	intron-variant	ARHGAP10	GRCh38.p7	4:147989437	taataagcctgggag[C/T]ggtatgggagactgg	79658
rs6841858	snp	C/G	0.265727	0.249505	intron-variant	ARHGAP10	GRCh38.p7	4:147989439	ataagcctgggagcg[C/G]tatgggagactggag	79658
rs6843392	snp	A/G	0.248471	0.249995	intron-variant	ARHGAP10	GRCh38.p7	4:147896299	gtattaaGtgtttga[A/G]gtaattcacctatga	79658
rs6843781	snp	A/G	0.0429648	0.14013	intron-variant	ARHGAP10	GRCh38.p7	4:147889502	atggggtttcaccat[A/G]ttggccaggctggtc	79658
rs6844045	snp	C/T	0.0162398	0.0886349	intron-variant	ARHGAP10	GRCh38.p7	4:147984637	gagcaggctcactgc[C/T]tcctgtaggaccagg	79658
rs6844257	snp	A/G	0.0329836	0.124112	intron-variant	ARHGAP10	GRCh38.p7	4:147831759	TTTCAGGAATGTACC[A/G]TTTGAGAGTTTAATT	79658
rs6845560	snp	A/G	0.434253	0.168969	intron-variant	ARHGAP10	GRCh38.p7	4:147766459	agtatgtaagcaacc[A/G]tcagttttttccctc	79658
rs6845865	snp	C/T	0.412917	0.189626	intron-variant	ARHGAP10	GRCh38.p7	4:148053451	TGGTTGCTGCGCATT[C/T]ATCATCTAACACCTT	79658
rs6846526	snp	C/T	0.453453	0.145282	intron-variant	ARHGAP10	GRCh38.p7	4:147857110	gcccgtcttggcctc[C/T]caaagtgctgagatt	79658
rs6846899	snp	C/T	0.3744	0.216852	intron-variant	ARHGAP10	GRCh38.p7	4:147840946	ACTCAAGATGATCCT[C/T]TCAGGCAGGGTTTGG	79658
rs6848211	snp	A/G	0.0418186	0.138422	intron-variant	ARHGAP10	GRCh38.p7	4:147814713	ATGATCTTTAAAAAC[A/G]Atgctttgaaatagt	79658
rs6849257	snp	C/G	0.267636	0.249377	intron-variant	ARHGAP10	GRCh38.p7	4:147990820	aaactgcctattaga[C/G]cctgggcaacatggt	79658
rs6849336	snp	A/G	0.211212	0.246973	intron-variant	ARHGAP10	GRCh38.p7	4:147744286	GTGCAGGGAAAATGC[A/G]TCTGAGAGGTCAGAG	79658
rs6850705	snp	A/G	0.0433465	0.140692	intron-variant	ARHGAP10	GRCh38.p7	4:147890569	cagtggcccatgcct[A/G]taatcccagcacttt	79658
rs6851336	snp	A/G	0.145978	0.227331	intron-variant	ARHGAP10	GRCh38.p7	4:147890803	ttggactccagcctg[A/G]gcaacagagcgagac	79658
rs6852320	snp	A/G	0.23031	0.249223	intron-variant	ARHGAP10	GRCh38.p7	4:147860913	GAAGGAAATCATTTT[A/G]TGACCCTAGTTACAA	79658
rs6853296	snp	A/G	0.453331	0.145452	intron-variant	ARHGAP10	GRCh38.p7	4:147850673	actgtaacactcact[A/G]cgagggtccgcggct	79658
rs6853436	snp	G/T	0.0107246	0.0724382	intron-variant	ARHGAP10	GRCh38.p7	4:147760400	TCAGGTTTCTACTTG[G/T]CAACGTCAGGGTTTG	79658
rs6853610	snp	C/T	0.211819	0.247067	intron-variant	ARHGAP10	GRCh38.p7	4:147885849	TGTAATATGTAGTTT[C/T]CTTACCCTTTTCTGT	79658
rs6853741	snp	A/G	0.434976	0.168179	intron-variant	ARHGAP10	GRCh38.p7	4:148061408	CAGGGCTTCACTCAC[A/G]CCTACCTGTCCTTTC	79658
rs6854640	snp	A/C	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147998395	GAGTCAGATATTTTC[A/C]CTGCTGAATGCTTTA	79658
rs6855559	snp	A/G	0.00953873	0.0683987	intron-variant	ARHGAP10	GRCh38.p7	4:147873738	ctcttggcctggtgt[A/G]gtggtgtgcgcctgt	79658
rs6856071	snp	A/G	0.141934	0.225437	intron-variant	ARHGAP10	GRCh38.p7	4:147873728	cacacacacactctt[A/G]gcctggtgtagtggt	79658
rs6856135	snp	A/G	0.267636	0.249377	intron-variant	ARHGAP10	GRCh38.p7	4:147998938	AGAACTAGACAAGAA[A/G]AGAGAAGAGAGGGAA	79658
rs6856145	snp	A/G	0.399253	0.200558	intron-variant	ARHGAP10	GRCh38.p7	4:148022050	TGTTAGTTGTTCAGC[A/G]ATACACATATGTAAG	79658
rs6856273	snp	C/T	0.414905	0.187899	intron-variant	ARHGAP10	GRCh38.p7	4:147894939	tcattagtcaggtgg[C/T]acaagtcctctgttc	79658
rs6857490	snp	A/C	0.109461	0.206758	intron-variant	ARHGAP10	GRCh38.p7	4:147921484	GGGACAGAAGATGCC[A/C]CAGGGGCTTTCCTGA	79658
rs6857492	snp	C/T	0.0475351	0.146656	intron-variant	ARHGAP10	GRCh38.p7	4:147861318	ctgggaacacggtgg[C/T]acccggaaacttgga	79658
rs6857710	snp	A/C	0.0441095	0.141807	intron-variant	ARHGAP10	GRCh38.p7	4:147861441	tctccttctcgtcgc[A/C]cacaatgtagtgagc	79658
rs6857825	snp	G/T	0.5	0	intron-variant	ARHGAP10	GRCh38.p7	4:147912578	atatatatatatata[G/T]atatatatatatata	79658
rs7356303	snp	A/G	0.356169	0.226336	intron-variant	ARHGAP10	GRCh38.p7	4:147977719	acagggatatattac[A/G]tggtgttgaagttgg	79658
rs7435763	snp	A/G	0.157642	0.232314	intron-variant	ARHGAP10	GRCh38.p7	4:147853092	gggtcgcaggtggct[A/G]gagcccatttcagca	79658
rs7441768	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147732943	CCAGAGTCCCCTTAA[A/G]CTTCACCTTTTCCCT	79658
rs7654433	snp	C/T	0.41408	0.188621	intron-variant	ARHGAP10	GRCh38.p7	4:147858742	GCTTTTACAGGCCCC[C/T]TTTATGCTAGCAGTT	79658
rs7654818	snp	C/T	0.141258	0.225111	intron-variant	ARHGAP10	GRCh38.p7	4:147870190	AGTTCATGCCATCCT[C/T]CTGCCTGTAGTCCCA	79658
rs7655236	snp	C/G	0.255224	0.249945	intron-variant	ARHGAP10	GRCh38.p7	4:147821806	AGTGCAGAAGTCAGT[C/G]AACACCTTCTTAGAA	79658
rs7655265	snp	A/C	0.342358	0.232314	intron-variant	ARHGAP10	GRCh38.p7	4:147916903	AGCAAACTCCCAGAT[A/C]CCATTCTTTGCTTGC	79658
rs7656471	snp	C/T	0.338296	0.233889	intron-variant	ARHGAP10	GRCh38.p7	4:147870990	TTTGAGATGGAGTCT[C/T]GCTCTGTTGCCCAGG	79658
rs7657316	snp	C/G	0.0923359	0.194016	intron-variant	ARHGAP10	GRCh38.p7	4:147992563	GGCGCCCACCACCAA[C/G]CCCAGCTAATTTTTG	79658
rs7658486	snp	C/T	0.157642	0.232314	intron-variant	ARHGAP10	GRCh38.p7	4:147963038	TTTCCTATTCTAATC[C/T]ATCCTTTAAGAAAAA	79658
rs7660368	snp	C/T	0.495291	0.0482933	intron-variant	ARHGAP10	GRCh38.p7	4:148066821	TGTATTAAGATAGCA[C/T]TGGGGCTACTAGAAA	79658
rs7660425	snp	C/T	0.121717	0.214577	intron-variant	ARHGAP10	GRCh38.p7	4:147883946	gggatccacctgcct[C/T]ggcctcccaaagtgc	79658
rs7660495	snp	A/G	0.0162398	0.0886349	intron-variant	ARHGAP10	GRCh38.p7	4:147988007	GTGAGAAAATACAGA[A/G]TGTGAGGCACTTGCA	79658
rs7660508	snp	A/G	0.450483	0.149354	intron-variant	ARHGAP10	GRCh38.p7	4:147887211	gctgtttcccgctct[A/G]gacacccacctccac	79658
rs7660688	snp	C/G	0.248471	0.249995	intron-variant	ARHGAP10	GRCh38.p7	4:147887243	ctcagtgcccagaca[C/G]cctgcctttcctccc	79658
rs7660941	snp	C/T	0.0825414	0.185628	intron-variant	ARHGAP10	GRCh38.p7	4:147813257	CCGAGTTGTCACTCA[C/T]GGCCTCTGCTAGCTA	79658
rs7661267	snp	C/T	0.147656	0.228091	intron-variant	ARHGAP10	GRCh38.p7	4:147887552	tcttcaaaaagctat[C/T]atatttatggtctca	79658
rs7661589	snp	A/G	0.0197687	0.0974348	intron-variant	ARHGAP10	GRCh38.p7	4:147880555	AATATGTTATGGAAT[A/G]TAACTGTGAGATTTT	79658
rs7663215	snp	C/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147817570	CCTACCTCTCAAACT[C/T]AGCACATCTCAAATA	79658
rs7663257	snp	C/G	0.0142736	0.0832652	intron-variant	ARHGAP10	GRCh38.p7	4:147780209	GCACTCGTTTCACTT[C/G]CCCTTTTCTGTGGCT	79658
rs7663294	snp	C/G	0.333261	0.235728	intron-variant	ARHGAP10	GRCh38.p7	4:147875313	CATGTTTAGGAGAAA[C/G]ACATTCCAGCCCTGG	79658
rs7663654	snp	A/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147817847	TTCACAATACTCAGG[A/G]ATTAGCAGGCAGAAG	79658
rs7663748	snp	A/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147817662	CTCCTATTTGCCTGT[A/G]GATCAAGACACAAAA	79658
rs7663821	snp	A/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147817907	TGATTTTTCCATTTA[A/G]TTGCAATTCTGCACT	79658
rs7664145	snp	A/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147817825	GGTATCTCAAGAGCA[A/G]TATTAATTCACAATA	79658
rs7664520	snp	A/G	0.202343	0.245416	intron-variant	ARHGAP10	GRCh38.p7	4:148023985	CGTCCCTTCCGAGCC[A/G]TGCTGTTCAGCTAAT	79658
rs7664567	snp	G/T	0.41325	0.18934	intron-variant	ARHGAP10	GRCh38.p7	4:147859578	agggcccagcctatt[G/T]tttttcatagtctta	79658
rs7665667	snp	A/C	0.390651	0.206682	intron-variant	ARHGAP10	GRCh38.p7	4:147988437	TCTGGCCTGCCGGTC[A/C]TTTGGTCAGGTAGCA	79658
rs7666035	snp	C/T	0.0119091	0.0762411	intron-variant	ARHGAP10	GRCh38.p7	4:148069212	CCTTATCTGCAACTG[C/T]GGAGCCACTTTTCCT	79658
rs7666127	snp	A/G	0.221439	0.248363	intron-variant	ARHGAP10	GRCh38.p7	4:147863329	ctctaggtgtctcat[A/G]tgagtgggatcatat	79658
rs7666206	snp	C/T	0.335788	0.23482	intron-variant	ARHGAP10	GRCh38.p7	4:147923696	AAGCAAATTTATCTT[C/T]CTTTGCAAAGCAAAG	79658
rs7666432	snp	A/G	0.0352966	0.128072	intron-variant	ARHGAP10	GRCh38.p7	4:148069278	CTTGTAGCCCACCTC[A/G]CCCACTGCTCAGCTG	79658
rs7666483	snp	A/G	0.0352966	0.128072	intron-variant	ARHGAP10	GRCh38.p7	4:148069491	GCCTTGGTTTCCCCA[A/G]TCAAGCCTCCTTTCA	79658
rs7666812	snp	A/G	0.000399281	0.0141238	intron-variant	ARHGAP10	GRCh38.p7	4:148011909	TTTGAATTACATAAA[A/G]ATCTATGTGCTAATC	79658
rs7666885	snp	A/G	0.393065	0.205018	intron-variant	ARHGAP10	GRCh38.p7	4:148011692	acggaaagagtgtca[A/G]agaatttgtggccat	79658
rs7667283	snp	A/G	0.00279162	0.0372561	intron-variant	ARHGAP10	GRCh38.p7	4:148011942	CCAGTAACTAAACGC[A/G]TAAGAATAACAGATA	79658
rs7667784	snp	C/T	0.0023933	0.0345097	intron-variant	ARHGAP10	GRCh38.p7	4:147973104	GATCAACTTGTAAGA[C/T]GTATGTGAATGAGTG	79658
rs7668368	snp	C/T	0.0704125	0.17392	intron-variant	ARHGAP10	GRCh38.p7	4:147999468	ctgccattgcagccc[C/T]accactgacttccat	79658
rs7668569	snp	A/G	0.383632	0.211288	intron-variant	ARHGAP10	GRCh38.p7	4:148029722	TAACTTCCCAAGCCC[A/G]GAAGCCCTTTGCCAT	79658
rs7669783	snp	A/G	0.36315	0.222928	intron-variant	ARHGAP10	GRCh38.p7	4:147912157	Cttttaaaatgaatt[A/G]tagttattaatttta	79658
rs7669809	snp	C/G	0.273318	0.24891	intron-variant	ARHGAP10	GRCh38.p7	4:147753498	ataggtgtgcaccac[C/G]gtacctggctaattt	79658
rs7670230	snp	C/T	0.283158	0.247791	intron-variant	ARHGAP10	GRCh38.p7	4:147832419	tttgggaggccgagg[C/T]gggtggatcttgagg	79658
rs7670524	snp	A/G	0.0352966	0.128072	intron-variant	ARHGAP10	GRCh38.p7	4:147936625	tgagccaccgcgccc[A/G]gccCTTTTCCTCTCT	79658
rs7672161	snp	A/G	0.321292	0.23962	intron-variant	ARHGAP10	GRCh38.p7	4:147924249	TTCCTCTGAGACGGC[A/G]AACCCCGAGTCCTTG	79658
rs7672409	snp	C/T	0.445855	0.155373	intron-variant	ARHGAP10	GRCh38.p7	4:147829478	acagatgtgagccac[C/T]gcgcccggccAGGAC	79658
rs7673234	snp	A/G	0.43978	0.162738	intron-variant	ARHGAP10	GRCh38.p7	4:147769762	TCCTGAACTTTTCAG[A/G]TAAGAAACTATAGGA	79658
rs7673606	snp	A/G	0.439502	0.163061	intron-variant	ARHGAP10	GRCh38.p7	4:147769890	CCTGAAGGGACTGCC[A/G]CTTTTCTCTAGCAGT	79658
rs7674116	snp	A/C	0.396727	0.202413	intron-variant	ARHGAP10	GRCh38.p7	4:147977237	ATATTCCCAGGAACA[A/C]CAAGACTACTTGGAA	79658
rs7675072	snp	C/T	0.297636	0.24542	intron-variant	ARHGAP10	GRCh38.p7	4:147764619	ACTCCCTGCAACCTC[C/T]GCCTCTTGGGTTCAA	79658
rs7675343	snp	A/G	0.417683	0.185425	intron-variant	ARHGAP10	GRCh38.p7	4:147736957	TCTCTCATGATGCCT[A/G]GGACTGCTACCCACT	79658
rs7677034	snp	G/T	0.231482	0.249313	intron-variant	ARHGAP10	GRCh38.p7	4:147745687	tagtagagacggggt[G/T]tcaccgtgttagcca	79658
rs7677632	snp	A/G	0.343701	0.231776	intron-variant	ARHGAP10	GRCh38.p7	4:147900831	AATTCAACAACAACA[A/G]CAACAACAACAACAC	79658
rs7677650	snp	A/C	0.000399281	0.0141238	intron-variant	ARHGAP10	GRCh38.p7	4:147870777	AGAGACTAGAATAGA[A/C]TTCTTCCTGGAAGGA	79658
rs7677894	snp	A/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147813160	TTTTTTTTAAATAAA[A/G]GAATTGTATGTGTTA	79658
rs7678334	snp	C/T	0.362313	0.223351	intron-variant	ARHGAP10	GRCh38.p7	4:148017180	agagaaacccagcaa[C/T]gcctgactgttcaga	79658
rs7678360	snp	A/G	0.0107246	0.0724382	intron-variant	ARHGAP10	GRCh38.p7	4:147830275	GTACTAAGCTGCTGC[A/G]TACCAAAGGCTTTTG	79658
rs7678505	snp	C/G	0.235273	0.249566	intron-variant	ARHGAP10	GRCh38.p7	4:147830239	GGTGACCTGCCCTGA[C/G]CTTTTGCCCCTATAG	79658
rs7680867	snp	C/T	0.119978	0.213528	intron-variant	ARHGAP10	GRCh38.p7	4:147786198	AACCTTATTAGCTGG[C/T]AGCTGGAGAGCCTGG	79658
rs7682961	snp	C/T	0.323197	0.239044	intron-variant	ARHGAP10	GRCh38.p7	4:147962936	AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACTG	79658
rs7683103	snp	A/G	0.344147	0.231595	intron-variant	ARHGAP10	GRCh38.p7	4:147813476	TGAGAATTTTAATTT[A/G]GGAAATCAGAAGGAA	79658
rs7683604	snp	G/T			intron-variant	ARHGAP10	GRCh38.p7	4:147813477	GAGAATTTTAATTTA[G/T]GAAATCAGAAGGAAA	79658
rs7683761	snp	A/G	0.000399281	0.0141238	intron-variant	ARHGAP10	GRCh38.p7	4:147813498	CAGAAGGAAAAAGCC[A/G]TGGGAGCCGAAATTG	79658
rs7684897	snp	C/T	0.249886	0.25	intron-variant	ARHGAP10	GRCh38.p7	4:147740106	CAGGCTGGAGTGCAG[C/T]GGTGTGATCTTGGCT	79658
rs7684915	snp	C/T			intron-variant	ARHGAP10	GRCh38.p7	4:148050108	ctgacctcaagtgat[C/T]cgcctgccttggctt	79658
rs7685405	snp	C/T	0.00199481	0.0315187	intron-variant	ARHGAP10	GRCh38.p7	4:147822257	GGCTGGAGTGGTTAT[C/T]TGGCAATTGGTTAAG	79658
rs7685779	snp	A/G	0.299664	0.245017	intron-variant	ARHGAP10	GRCh38.p7	4:147919266	AATATATTTTGGTAG[A/G]ACTGGCAGTTACTTA	79658
rs7685847	snp	A/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147743868	tttttaaagtactta[A/G]aaaaattgcctgaac	79658
rs7687208	snp	C/G	0.00119737	0.0244387	intron-variant	ARHGAP10	GRCh38.p7	4:147738291	GCGCGGTGGCTCACG[C/G]CTATAATCCCAGCAC	79658
rs7687859	snp	C/G	0.146985	0.227789	intron-variant	ARHGAP10	GRCh38.p7	4:147884211	TGAGACCTTGATCAT[C/G]CCCAATTTTCTTTTC	79658
rs7689751	snp	A/G	0.0501905	0.150254	intron-variant	ARHGAP10	GRCh38.p7	4:148057334	CCTCCTGAATATCCC[A/G]GTACTTGCATCTCTC	79658
rs7689903	snp	C/T	0.0414363	0.137845	intron-variant	ARHGAP10	GRCh38.p7	4:147988271	ATGGCTAAAACTTGT[C/T]TAACTTTATTTTTCA	79658
rs7691655	snp	A/T	0.375	0.216506	intron-variant	ARHGAP10	GRCh38.p7	4:147832357	ttttttttttttttt[A/T]aaaaGAGGAGTccag	79658
rs7694157	snp	C/T	0.109461	0.206758	intron-variant	ARHGAP10	GRCh38.p7	4:147936344	tttttttttttgaga[C/T]ggagtcttgctctgt	79658
rs7694397	snp	C/T	0.474453	0.110094	intron-variant	ARHGAP10	GRCh38.p7	4:148068353	CTTAAAAGCCTCTGG[C/T]GATTAAACTTTAAAG	79658
rs7694414	snp	C/T	0.0391387	0.134304	intron-variant	ARHGAP10	GRCh38.p7	4:148068383	GGTCTCAGATAGACA[C/T]AGAATAATCCCtgga	79658
rs7696511	snp	A/G	0.00199481	0.0315187	intron-variant	ARHGAP10	GRCh38.p7	4:148062042	GGCAAAGCTTGAGGC[A/G]GAGGTGGGAACGCCA	79658
rs7696624	snp	C/T	0.00119737	0.0244387	intron-variant	ARHGAP10	GRCh38.p7	4:148058726	ACTGCTGATCTGTTC[C/T]ATTTTCTAAAAATAC	79658
rs7697065	snp	A/G	0.000798403	0.0199641	intron-variant	ARHGAP10	GRCh38.p7	4:148059045	AGGAACGTGTTTCCA[A/G]GTTAGCAATTTGAAA	79658
rs7697204	snp	C/T	0.469937	0.118861	intron-variant	ARHGAP10	GRCh38.p7	4:148059023	GACTTTCAGTCTGTG[C/T]ATTTTCAGGAACGTG	79658
rs7697567	snp	A/G	0.265727	0.249505	intron-variant	ARHGAP10	GRCh38.p7	4:147873888	tttaaaaaaaaaaaa[A/G]aGGGGGGATAAGAAA	79658
rs7697568	snp	A/G	0.303688	0.244167	intron-variant	ARHGAP10	GRCh38.p7	4:147873889	ttaaaaaaaaaaaaa[A/G]GGGGGGATAAGAAAA	79658
rs7698166	snp	A/G	0.119978	0.213528	intron-variant	ARHGAP10	GRCh38.p7	4:147786113	TTAAAAGTAAGACAG[A/G]GGGAGACCCTGGGCT	79658
rs7698384	snp	C/T	0.00119737	0.0244387	intron-variant	ARHGAP10	GRCh38.p7	4:147745575	cagctcactgcaagc[C/T]ccgcctcctgggttc	79658
rs7698520	snp	A/T	0.497803	0.033074	intron-variant	ARHGAP10	GRCh38.p7	4:148007241	TCTTTCGGAAAGAGA[A/T]AATCAGAATAAAAGG	79658
rs7698670	snp	C/T	0.413748	0.188909	intron-variant	ARHGAP10	GRCh38.p7	4:147868391	gcaggtgcatgccag[C/T]acacccagctaattt	79658
rs7699081	snp	A/G	0.0162398	0.0886349	intron-variant	ARHGAP10	GRCh38.p7	4:147745771	gctgggattacaggt[A/G]tgagccactgtgccc	79658
rs7699281	snp	C/G	0.0146672	0.084371	intron-variant	ARHGAP10	GRCh38.p7	4:147861298	ggtcgcttccattgt[C/G]ggcactgggaacacg	79658
rs7699767	snp	C/G	0.00119737	0.0244387	intron-variant	ARHGAP10	GRCh38.p7	4:147986919	cttaagccctagact[C/G]tgctgCTGCTCCTTC	79658
rs7700162	snp	C/G	0.211819	0.247067	intron-variant	ARHGAP10	GRCh38.p7	4:147861977	atccctggcttgaag[C/G]tggggtttcaccagg	79658
rs9307842	snp	A/G	0.5	0	intron-variant	ARHGAP10	GRCh38.p7	4:147741792	CACACACACACACAC[A/G]CACACACACACACAC	79658
rs9307843	snp	C/T	0.23846	0.249734	intron-variant	ARHGAP10	GRCh38.p7	4:147838527	CTCTGGGATATGTTT[C/T]CATGATTTCTCTTCC	79658
rs9307844	snp	A/C			intron-variant	ARHGAP10	GRCh38.p7	4:147878942	ccactatgcctggct[A/C]attttttttagtaga	79658
rs9307845	snp	C/T	0.029116	0.117091	intron-variant	ARHGAP10	GRCh38.p7	4:147914568	CGCTCCCCCCCCCCC[C/T]TTTTTTTTTTTAACA	79658
rs9332471	snp	C/T	0.438246	0.16451	intron-variant	ARHGAP10	GRCh38.p7	4:147773019	CTGCATTCCAGAGTT[C/T]AGTGGTAAAAAGAAC	79658
rs9684012	snp	C/T	0.396182	0.202807	intron-variant	ARHGAP10	GRCh38.p7	4:147975879	CACACTGTGTTGTTT[C/T]ACTCTTGTTAACCCT	79658
rs9684069	snp	A/T			intron-variant	ARHGAP10	GRCh38.p7	4:147763772	ttttttttttttttt[A/T]aaaacagagttttgc	79658
rs9760912	snp	A/G	0.118933	0.212888	intron-variant	ARHGAP10	GRCh38.p7	4:148002518	tgtacctctggtaga[A/G]ttcggctgtgaatcc	79658
rs9762680	snp	C/G	0.279726	0.248226	intron-variant	ARHGAP10	GRCh38.p7	4:148002387	ctctttttttgttgt[C/G]tctctgccaggcttt	79658
rs9991394	snp	C/T	0.394538	0.203982	intron-variant	ARHGAP10	GRCh38.p7	4:148018942	CAAAGGCTGTTGAGA[C/T]TATTAAACTGCTTAT	79658
rs9991710	snp	A/T	0.0448719	0.142907	intron-variant	ARHGAP10	GRCh38.p7	4:147991157	acctaaaaaaaaaaa[A/T]aaataaataaaagaa	79658
rs9991741	snp	C/G	0.360842	0.224085	intron-variant	ARHGAP10	GRCh38.p7	4:147873177	cctttccaggactgg[C/G]gcagggaaagtataa	79658
rs9994150	snp	C/G	0.0279526	0.114869	intron-variant	ARHGAP10	GRCh38.p7	4:147738558	actctgtctcccccc[C/G]ccaaaaaaaattata	79658
rs9994275	snp	C/T	0.227369	0.248974	intron-variant	ARHGAP10	GRCh38.p7	4:148039519	tggccaggctgatct[C/T]gaattctggacctcc	79658
rs9994650	snp	C/T	0.253264	0.249979	intron-variant	ARHGAP10	GRCh38.p7	4:147894870	agattctctactctg[C/T]tgcatctctttgtct	79658
rs9995896	snp	C/T	0.206336	0.246157	intron-variant	ARHGAP10	GRCh38.p7	4:147825149	GGACACTGATTTGGA[C/T]TTAAAAAGTGACAGA	79658
rs9995956	snp	C/T	0.28578	0.247426	intron-variant	ARHGAP10	GRCh38.p7	4:147869222	CTGCATAGGTGAATG[C/T]CCTGAAGCCAGCTCT	79658
rs9996108	snp	A/G	0.217551	0.247885	intron-variant	ARHGAP10	GRCh38.p7	4:147832159	TTAATTGTCTAATCC[A/G]GAGGAGTGATTCGAT	79658
rs9996209	snp	A/G	0.188946	0.24243	intron-variant	ARHGAP10	GRCh38.p7	4:147869355	CACACCTGTTGGGGG[A/G]GCGTCTGTTTACCTT	79658
rs9996365	snp	C/T	0.0592355	0.161582	intron-variant	ARHGAP10	GRCh38.p7	4:147735379	ACAAGGGTTTGTATG[C/T]TAGAGTGGAGGAGGT	79658
rs9997027	snp	A/T	0.28578	0.247426	intron-variant	ARHGAP10	GRCh38.p7	4:147870848	AGAAGATAACAAGAA[A/T]GGGTAGGAAGTATTT	79658
rs9997153	snp	C/T	0.0154538	0.0865337	intron-variant	ARHGAP10	GRCh38.p7	4:147799515	tgcttattttcacag[C/T]ctgttttctattgtt	79658
rs9997304	snp	C/T	0.0596104	0.162024	intron-variant	ARHGAP10	GRCh38.p7	4:147739502	TTGAGGACGTGAACT[C/T]AAAATTAGGGTTTCT	79658
rs9998229	snp	A/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147836040	TTTCCTAAGTGTACT[A/T]AAAAACAAATCTTTA	79658
rs9999132	snp	C/G/T			intron-variant	ARHGAP10	GRCh38.p7	4:147870008	CCAGTTtgtgtgtgt[C/G/T]tgtgtgtgtgtgtgt	79658
rs9999321	snp	A/G	0.285519	0.247464	intron-variant	ARHGAP10	GRCh38.p7	4:147870221	CCTGCCACCATGCCC[A/G]GCTAATTTTTTTGTA	79658
rs10000278	snp	C/T	0.313326	0.241847	intron-variant	ARHGAP10	GRCh38.p7	4:147871916	GACCAGCCTGGGCAA[C/T]GTAGTGAGACCCTGT	79658
rs10001150	snp	A/T			intron-variant	ARHGAP10	GRCh38.p7	4:147788290	tctctattaaaaata[A/T]aaaaaaattagccag	79658
rs10001327	snp	A/T	0.337158	0.234315	intron-variant	ARHGAP10	GRCh38.p7	4:147788458	TCTCAAAAAGAAAAA[A/T]AAAAGTGCTTCTGAG	79658
rs10001688	snp	A/G	0.232067	0.249356	intron-variant	ARHGAP10	GRCh38.p7	4:147876486	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	79658
rs10001756	snp	A/G	0.295088	0.245901	intron-variant	ARHGAP10	GRCh38.p7	4:147876520	ATGGCGTGAACCTGG[A/G]AGGCGGAGCTTGCAG	79658
rs10002113	snp	C/G/T	0.0162398	0.0886349	intron-variant	ARHGAP10	GRCh38.p7	4:147745909	ctcctgcctcagcct[C/G/T]ctgagtagctgggat	79658
rs10002792	snp	A/T	0.380529	0.213219	intron-variant	ARHGAP10	GRCh38.p7	4:147959747	GTGTATGTGCCACAT[A/T]TTCTTAATCCAGGTT	79658
rs10002890	snp	A/G	0.205417	0.245993	intron-variant	ARHGAP10	GRCh38.p7	4:148012585	GTTTAGAAACATTTC[A/G]GTTGGATGGTAAGAT	79658
rs10003056	snp	A/G	0.0162398	0.0886349	intron-variant	ARHGAP10	GRCh38.p7	4:147746782	CATGACAGAGGAGAT[A/G]GTAAATGATGTCTAC	79658
rs10003349	snp	A/G	0.48955	0.071525	intron-variant	ARHGAP10	GRCh38.p7	4:148007062	GCGGTGGGAGTTAGC[A/G]CACTTCAAGGAGGTT	79658
rs10003507	snp	C/T	0.279726	0.248226	intron-variant	ARHGAP10	GRCh38.p7	4:147903165	CTGCCTCCACAGCTT[C/T]CTGTTGTGCCACTCT	79658
rs10004138	snp	A/G	0.325327	0.238382	intron-variant	ARHGAP10	GRCh38.p7	4:147882688	TCTGTTTATTCAAAG[A/G]TGAATTCTTTTTTTT	79658
rs10004457	snp	C/G	0.0162398	0.0886349	intron-variant	ARHGAP10	GRCh38.p7	4:147751805	AAGAACGTGGGTTTA[C/G]AGAGGTTGACATTTG	79658
rs10004691	snp	C/G	0.251014	0.249998	intron-variant	ARHGAP10	GRCh38.p7	4:147907315	TTTTGATGGACTAGT[C/G]GCTTTTGAGAGTTGA	79658
rs10004792	snp	A/G	0.290977	0.246619	intron-variant	ARHGAP10	GRCh38.p7	4:147907482	ATCTGGAAAGCATTT[A/G]CCAGTTCAGCATTGT	79658
rs10004850	snp	C/T	0.282632	0.247861	intron-variant	ARHGAP10	GRCh38.p7	4:147838362	ataattccagctact[C/T]aggaggctgaggcag	79658
rs10004995	snp	C/T	0.0170251	0.090679	intron-variant	ARHGAP10	GRCh38.p7	4:147752588	tgttgcttaggctgg[C/T]gtgatcttggctcac	79658
rs10005192	snp	C/T	0.114036	0.209795	intron-variant	ARHGAP10	GRCh38.p7	4:147806972	CAAGTCTCTAGTAAG[C/T]GTGAAACCCGGTGAA	79658
rs10005261	snp	C/T	0.0170251	0.090679	intron-variant	ARHGAP10	GRCh38.p7	4:147746829	TTTATGGCAGGACAT[C/T]GAGGAAACTGTCAAC	79658
rs10005413	snp	C/T	0.209084	0.246629	intron-variant	ARHGAP10	GRCh38.p7	4:147982891	ACtttcttttttttc[C/T]tgaattttcgagaca	79658
rs10005695	snp	C/T	0.199873	0.244923	intron-variant	ARHGAP10	GRCh38.p7	4:148048098	ATAGTGCTGGGATTA[C/T]AGGTGTGAACCACCA	79658
rs10006169	snp	G/T	0.198324	0.244601	intron-variant	ARHGAP10	GRCh38.p7	4:148048467	ATGCTGAGGATTGTG[G/T]ATTTAAATCCTACAT	79658
rs10006193	snp	C/T	0.168135	0.236216	intron-variant	ARHGAP10	GRCh38.p7	4:147768769	TTTGGCAGGGAATCT[C/T]GCTCTGTCACCCAGA	79658
rs10006246	snp	C/T	0.227664	0.249	intron-variant	ARHGAP10	GRCh38.p7	4:148039585	GATTACAGGTGTGAG[C/T]CACCACACCCGGCCT	79658
rs10007231	snp	C/G	0.237882	0.249706	intron-variant	ARHGAP10	GRCh38.p7	4:147853634	GTTTTTTGCAAAAAA[C/G]TGCTTAATGAAGAAT	79658
rs10008133	snp	C/T	0.0349115	0.127424	intron-variant	ARHGAP10	GRCh38.p7	4:148054371	ATAATAACATCTGCC[C/T]CTCTGGGCCGGGGTG	79658
rs10009344	snp	A/G	0.0158469	0.0875917	intron-variant	ARHGAP10	GRCh38.p7	4:148014560	CATTTGGTTCTGAGC[A/G]TATTATCAAAGTTAT	79658
rs10010556	snp	A/G	0.0592355	0.161582	intron-variant	ARHGAP10	GRCh38.p7	4:147972698	GGCAAGTATGAGGAC[A/G]GGCTAGTGATGTGAG	79658
rs10010960	snp	C/T	0.362104	0.223456	intron-variant	ARHGAP10	GRCh38.p7	4:147870174	TCCTGCCTGTAGTCC[C/T]AGTTCATGCCATCCT	79658
rs10010996	snp	G/T	0.0869089	0.189476	intron-variant	ARHGAP10	GRCh38.p7	4:148054840	CCCATAAATCTCTTT[G/T]TAAGTGATTGGTGGA	79658
rs10011328	snp	C/T	0.147656	0.228091	intron-variant	ARHGAP10	GRCh38.p7	4:147775443	GTCTTAGGGGCCAGC[C/T]TCAGGGGCCAGTGAC	79658
rs10011891	snp	C/T	0.0596104	0.162024	intron-variant	ARHGAP10	GRCh38.p7	4:147739939	tggggtttcaccaca[C/T]tggccaggctggtct	79658
rs10012122	snp	A/G	0.0644693	0.167566	intron-variant	ARHGAP10	GRCh38.p7	4:147802324	AAATGAGATGTTCAG[A/G]AGTTAGGGTGAAGCT	79658
rs10012580	snp	C/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147770790	TGTATGACAGTtgta[C/T]gattctgctaggaca	79658
rs10013038	snp	C/T	0.279726	0.248226	intron-variant	ARHGAP10	GRCh38.p7	4:147854986	GCTGGGTGTTTTGAC[C/T]GCTGATTAAAGCGTC	79658
rs10013413	snp	C/T	0.444666	0.15686	intron-variant	ARHGAP10	GRCh38.p7	4:148061127	GAAAGATGTGAGGAT[C/T]AAGCAGACAATACCT	79658
rs10014593	snp	A/G	0.278664	0.248351	intron-variant	ARHGAP10	GRCh38.p7	4:147910640	GCCACTGCTGTACTT[A/G]AAGAAAATGAAACAT	79658
rs10014696	snp	A/G	0.298144	0.245321	intron-variant	ARHGAP10	GRCh38.p7	4:147873645	AGCCTGGGCCCCATA[A/G]TGAGACCCCTGTCTC	79658
rs10015875	snp	G/T	0.252702	0.249985	intron-variant	ARHGAP10	GRCh38.p7	4:147891518	TAGGGTGATAAAAAT[G/T]TTCTAAAATTGATTT	79658
rs10016632	snp	A/G	0.00953873	0.0683987	intron-variant	ARHGAP10	GRCh38.p7	4:147944331	ATGTAATCAGTGTCA[A/G]TTGCCATTGTTGTAG	79658
rs10016720	snp	A/G	0.0205511	0.0992634	intron-variant	ARHGAP10	GRCh38.p7	4:147856362	CGTATTTTAAATAGC[A/G]TTACAGAAATCACTG	79658
rs10016881	snp	C/T	0.0170251	0.090679	intron-variant	ARHGAP10	GRCh38.p7	4:147752488	AAAAAGTAATGTTAC[C/T]GTTAATGATTTAATA	79658
rs10018553	snp	C/T	0.217551	0.247885	intron-variant	ARHGAP10	GRCh38.p7	4:147832082	TCCCCCTGACTGCCC[C/T]GCCCGACATACACAC	79658
rs10018820	snp	A/G	0.188946	0.24243	intron-variant	ARHGAP10	GRCh38.p7	4:147869716	TTAATAAACACTCTT[A/G]CAACTCAGAGTTTCT	79658
rs10018903	snp	A/G	0.217551	0.247885	intron-variant	ARHGAP10	GRCh38.p7	4:147832201	TGTGCAGCTGAGTCT[A/G]CTGTTTCACTAGGGA	79658
rs10021285	snp	A/G	0.0123036	0.0774623	intron-variant	ARHGAP10	GRCh38.p7	4:147930217	GAATCATACGGCTGC[A/G]AAATCCTTTTTAATC	79658
rs10021322	snp	C/T	0.000399281	0.0141238	intron-variant	ARHGAP10	GRCh38.p7	4:148018001	TGTCACTCTGAACAG[C/T]GGTGCCAGACTTCTG	79658
rs10021480	snp	C/T	0.283947	0.247685	intron-variant	ARHGAP10	GRCh38.p7	4:147978960	attctggaaattagt[C/T]ctttgtcagatgcat	79658
rs10021566	snp	G/T	0.0111196	0.0737302	intron-variant	ARHGAP10	GRCh38.p7	4:148009167	gatggagtcttgctt[G/T]gtcgctcagctggag	79658
rs10021664	snp	A/G	0.0138799	0.0821421	intron-variant	ARHGAP10	GRCh38.p7	4:147951045	TTGCAGTGACTCAGC[A/G]TAATACATTCTGTAT	79658
rs10021682	snp	A/G	0.021333	0.101051	intron-variant	ARHGAP10	GRCh38.p7	4:147988172	ACAGATGGAGCGTGT[A/G]TGTCTGGTCAACATA	79658
rs10021936	snp	G/T	0.237593	0.249692	intron-variant	ARHGAP10	GRCh38.p7	4:147854237	TCGTGTTGTTACAAT[G/T]AAGAAAAAATGTGTT	79658
rs10021991	snp	G/T	0.179105	0.239737	intron-variant	ARHGAP10	GRCh38.p7	4:147988434	TCCTCTGGCCTGCCG[G/T]TCCTTTGGTCAGGTA	79658
rs10022144	snp	A/T	0.279726	0.248226	intron-variant	ARHGAP10	GRCh38.p7	4:147854408	ACTATCTGGTTTTCA[A/T]TGCCTACCACTCCTG	79658
rs10022691	snp	A/G	0.282105	0.24793	intron-variant	ARHGAP10	GRCh38.p7	4:147858039	ATTATGCGTTTATGT[A/G]AAGGCAGCATTAATC	79658
rs10022963	snp	A/T	0.210605	0.246877	intron-variant	ARHGAP10	GRCh38.p7	4:147851307	TTGTCCAGGCTGGGC[A/T]GCAGCCTTGAACTCC	79658
rs10023057	snp	C/G	0.325563	0.238307	intron-variant	ARHGAP10	GRCh38.p7	4:147858397	ACATTATGTACTACT[C/G]TCATAAACACTTATT	79658
rs10023419	snp	A/G	0.0596104	0.162024	intron-variant	ARHGAP10	GRCh38.p7	4:147733645	CATTTTTCAGTAAGG[A/G]CGATTAAAACATATT	79658
rs10023855	snp	A/C	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147751193	caaaaccaaaaacaa[A/C]aaaaacaaaCAATGA	79658
rs10024194	snp	G/T	0.078151	0.181571	intron-variant	ARHGAP10	GRCh38.p7	4:147749613	AAATCAATTGAGAAA[G/T]CCTTTAAGCATCTAG	79658
rs10024385	snp	A/G	0.0150606	0.0854603	intron-variant	ARHGAP10	GRCh38.p7	4:147806009	AATATTTTCCACCCA[A/G]TGAGCCCtttattat	79658
rs10024476	snp	C/T	0.0134861	0.0810011	intron-variant	ARHGAP10	GRCh38.p7	4:147914800	tttgtgtttctgttT[C/T]AAATTTAGGGAAAAC	79658
rs10025069	snp	C/T	0.253824	0.249971	intron-variant	ARHGAP10	GRCh38.p7	4:147894460	aaacaaatcatttac[C/T]ggatataataatagt	79658
rs10025180	snp	C/T	0.376989	0.215346	intron-variant	ARHGAP10	GRCh38.p7	4:147959523	CCCTCCCCGCTCCCC[C/T]CACCCCACGACAGGC	79658
rs10025355	snp	A/G	0.00874735	0.0655527	intron-variant	ARHGAP10	GRCh38.p7	4:147959516	atgctatccctcccc[A/G]ctccccccaccccac	79658
rs10025443	snp	A/G	0.380138	0.213458	intron-variant	ARHGAP10	GRCh38.p7	4:148006851	GGGAGAGTCAGCTCC[A/G]TGGCTAAGATTTCCA	79658
rs10025684	snp	A/G	0.282895	0.247826	intron-variant	ARHGAP10	GRCh38.p7	4:147858823	CTTCATTCCCCAAGT[A/G]AATTTCCAAATCCAC	79658
rs10025959	snp	G/T			intron-variant	ARHGAP10	GRCh38.p7	4:147733913	CTGCTGCTTGAATCA[G/T]AAATGGGACTCTGGG	79658
rs10026985	snp	A/G	0.295088	0.245901	intron-variant	ARHGAP10	GRCh38.p7	4:147877322	TTAAAACACAAAGCA[A/G]TGTTTCCCAAATTCA	79658
rs10027182	snp	A/G	0.424659	0.17887	intron-variant	ARHGAP10	GRCh38.p7	4:148060255	TATTACATTTTAGAT[A/G]ATATTTAAAAAATGT	79658
rs10027275	snp	C/G	0.445196	0.1562	intron-variant	ARHGAP10	GRCh38.p7	4:148060345	CGAAGCTCATGTTTA[C/G]TTTTTTTTTTTTTTT	79658
rs10027347	snp	G/T	0.125874	0.217008	intron-variant	ARHGAP10	GRCh38.p7	4:148025539	AATAGTTATTTCAGA[G/T]AGAACAGAGTAGGGT	79658
rs10027921	snp	C/T	0.428635	0.174898	intron-variant	ARHGAP10	GRCh38.p7	4:147790984	GTGGATTTGGGATGT[C/T]TCATTGCCACATATG	79658
rs10028956	snp	C/T	0.000399281	0.0141238	intron-variant	ARHGAP10	GRCh38.p7	4:147920489	AAGAAAATAGCAGAA[C/T]GTTCTTTTTGTTCCC	79658
rs10029385	snp	A/C	0.24019	0.249807	intron-variant	ARHGAP10	GRCh38.p7	4:147819814	TCCGCCCGTCTCGGC[A/C]TCCCAGAGTGCTGGG	79658
rs10029636	snp	C/T	0.0588605	0.161139	intron-variant	ARHGAP10	GRCh38.p7	4:147759938	attttttagtagaga[C/T]ggtgtttcaccatgt	79658
rs10029666	snp	C/T	0.00993419	0.0697739	intron-variant	ARHGAP10	GRCh38.p7	4:147995817	cgcctcctgggttca[C/T]gccattctcctgcct	79658
rs10029825	snp	A/G	0.263535	0.249633	intron-variant	ARHGAP10	GRCh38.p7	4:147995796	ATCTCTGCTCACTGC[A/G]AGCTTCGCCTCCTGG	79658
rs10030122	snp	A/G	0.283158	0.247791	intron-variant	ARHGAP10	GRCh38.p7	4:147870930	CCAAAACTACAGACT[A/G]TGTGTGTGTGTGTGT	79658
rs10030358	snp	C/T	0.336017	0.234736	intron-variant	ARHGAP10	GRCh38.p7	4:147901395	CAAGTGTGAAGTGTT[C/T]TGAAGAATGTAGACT	79658
rs10030416	snp	A/T	0.0248432	0.108648	intron-variant	ARHGAP10	GRCh38.p7	4:147813749	AAGCAAGTTGCTCAC[A/T]TGTTTTCCTGGTCTC	79658
rs10030513	snp	A/G	0.233527	0.249457	intron-variant	ARHGAP10	GRCh38.p7	4:147848722	TGAGTGCGAGTGAAT[A/G]TATTTACTTTTACTT	79658
rs10031581	snp	A/G	0.0126979	0.078662	intron-variant	ARHGAP10	GRCh38.p7	4:148014746	GAAACCTTTAATGCA[A/G]AAACCAAAGTCTGCT	79658
rs10032488	snp	C/T	0.429837	0.173662	intron-variant	ARHGAP10	GRCh38.p7	4:147796686	GCCTGCCACCATGCC[C/T]GGCTAATTTTTTGTA	79658
rs10032952	snp	C/T	0.0126979	0.078662	intron-variant	ARHGAP10	GRCh38.p7	4:148017936	AGGGATTTATATAAA[C/T]GGCTGAGTCCCATGA	79658
rs10033226	snp	C/T	0.284995	0.247539	intron-variant	ARHGAP10	GRCh38.p7	4:147872095	caacagagtgagact[C/T]ggtcaaaaaaaaaaa	79658
rs10034181	snp	C/T	0.0558544	0.157504	intron-variant	ARHGAP10	GRCh38.p7	4:147741995	CACTTAATATTTCAA[C/T]GGTGAGTGTGATTTC	79658
rs10049932	snp	C/T	0.28052	0.24813	intron-variant	ARHGAP10	GRCh38.p7	4:147906782	ACTTGCATTCATTTT[C/T]ATGTTATTTTTGTGT	79658
rs10049955	snp	C/T	0.0142736	0.0832652	intron-variant	ARHGAP10	GRCh38.p7	4:147982369	tttctttctttcttt[C/T]ttttttttttttctt	79658
rs10049959	snp	G/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147982574	tttttttttttttgg[G/T]attttgtgttgagat	79658
rs10084795	snp	A/C	0.00914312	0.0669923	intron-variant	ARHGAP10	GRCh38.p7	4:147944449	TGTATGATGCTATGC[A/C]TGTGAAATAACCATC	79658
rs10213171	snp	C/G	0.203267	0.245593	intron-variant	ARHGAP10	GRCh38.p7	4:148016386	cacgcgcctaaagtc[C/G]taattacttaagagg	79658
rs10213376	snp	G/T	0.203882	0.245709	intron-variant	ARHGAP10	GRCh38.p7	4:148015263	ATGAGGGGTACTTTG[G/T]TGGAAAGAAGGGGTC	79658
rs10213378	snp	C/T	0.400504	0.199621	intron-variant	ARHGAP10	GRCh38.p7	4:148015335	GTTCTGGGAGTAAGG[C/T]CTGACTGCCACTGAC	79658
rs10213616	snp	A/G	0.0551013	0.156571	intron-variant	ARHGAP10	GRCh38.p7	4:147942583	ACTAtccttctctcc[A/G]tcctccttctcctgc	79658
rs10461235	snp	A/G	0.453939	0.144598	intron-variant	ARHGAP10	GRCh38.p7	4:147838946	TTAGGGCTATTTTAG[A/G]CTAAGATTCCTCAAA	79658
rs10461236	snp	A/G	0.345679	0.230967	intron-variant	ARHGAP10	GRCh38.p7	4:147839142	tctatctatctatct[A/G]tctgtctgtctgtct	79658
rs10519914	snp	A/G	0.256897	0.249905	intron-variant	ARHGAP10	GRCh38.p7	4:147756460	TGATGAGCACTGTTA[A/G]TATGAACTATACCAT	79658
rs10519917	snp	C/T	0.217851	0.247924	intron-variant	ARHGAP10	GRCh38.p7	4:147814493	ACCTGACAGCTAAAT[C/T]CCTACTAATATTTGC	79658
rs10519918	snp	C/T	0.157972	0.232445	intron-variant	ARHGAP10	GRCh38.p7	4:147849204	AAACATCTGTCCTTT[C/T]CATTAGGTTGTTAAA	79658
rs10519921	snp	C/T	0.304188	0.244057	intron-variant	ARHGAP10	GRCh38.p7	4:147916191	TTCTAATCACCGTTT[C/T]CATGTTCTAAATATG	79658
rs10519926	snp	A/G	0.396	0.202938	intron-variant	ARHGAP10	GRCh38.p7	4:147968717	CACTTTGCTAATAAC[A/G]TTCCTGACTTCTGCC	79658
rs10519927	snp	C/T	0.0962929	0.197165	intron-variant	ARHGAP10	GRCh38.p7	4:147968919	CCATGTTTTGGGACT[C/T]GGATCCTATAAACGT	79658
rs10519931	snp	A/G	0.138546	0.223781	intron-variant	ARHGAP10	GRCh38.p7	4:148062225	GCTGGCCAGGAGACC[A/G]TGCTGGTACTGAAGA	79658
rs10519932	snp	G/T	0.0869089	0.189476	intron-variant	ARHGAP10	GRCh38.p7	4:148062327	TGCTCGTGGAAACTG[G/T]TGTACTGGTTTAGCA	79658
rs10519933	snp	C/T	0.263535	0.249633	intron-variant	ARHGAP10	GRCh38.p7	4:147995286	AATGGTGTATACGCA[C/T]TGGTATGTTTTCAGA	79658
rs10519934	snp	C/T	0.0858192	0.188533	intron-variant	ARHGAP10	GRCh38.p7	4:147995032	CTGTGGATCTGTCTG[C/T]GGCCCTAGAAACACA	79658
rs10532529	in-del	-/CT	0.0103295	0.0711199	intron-variant	ARHGAP10	GRCh38.p7	4:147825188	CGCAGTGGCTGATGC[-/CT]CTGTAATCCCAGCAC	79658
rs10536719	in-del	-/AAG	0.0854556	0.188216	intron-variant	ARHGAP10	GRCh38.p7	4:147857817	AAGTCCTTGTGAAAC[-/AAG]AAAAAATAATGAATA	79658
rs10542620	in-del	-/TT			intron-variant	ARHGAP10	GRCh38.p7	4:147864066	CCCAGATAAATATTT[-/TT]AAGAGTAAAATTAGC	79658
rs10644018	in-del	-/TT/TTTG/TTTTTT/TTTTTTTGTC			intron-variant	ARHGAP10	GRCh38.p7	4:147869998	AAAAAAGTCCCAGTT[-/TT/TTTG/TTTTTT/TTTTTTTGTC]TGTGTGTGTGTGTGT	79658
rs10644088	in-del	-/TG/TGTG	0.369346	0.219673	intron-variant	ARHGAP10	GRCh38.p7	4:147736120	CTTAAATTGTCTAGC[-/TG/TGTG]TGTGTGTGTGTGTGT	79658
rs10661268	in-del	-/AATTA	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147771500	TAAAATGTATGATTA[-/AATTA]TTTTTGACTATAGTC	79658
rs10666704	in-del	-/TT/TTT	0.313082	0.241911	upstream-variant-2KB	ARHGAP10	GRCh38.p7	4:147730885	CTTTTTTTTTTTTTT[-/TT/TTT]GAGACATTGTCTCGC	79658
rs10712979	in-del	-/T	0.404733	0.196361	intron-variant	ARHGAP10	GRCh38.p7	4:147858344	TCCCACAAAATTGTA[-/T]TTTTTTTTCTTGTTT	79658
rs10857227	snp	A/T	0.429688	0.173817	intron-variant	ARHGAP10	GRCh38.p7	4:147797673	GCCTCAGCCTCCCAG[A/T]GTGCTGGGATTACAA	79658
rs10857228	snp	C/T	0.437118	0.165792	intron-variant	ARHGAP10	GRCh38.p7	4:148058549	GAGTTCTCTGGTGAT[C/T]GGTGCAACTGGTGTC	79658
rs11099669	snp	A/G	0.439641	0.162899	intron-variant	ARHGAP10	GRCh38.p7	4:147768360	CTTCCTGATAAGAAC[A/G]TACTAGTGGTTTTTT	79658
rs11099670	snp	C/G	0.422158	0.181278	intron-variant	ARHGAP10	GRCh38.p7	4:147851401	AATTATTTTTGTAGA[C/G]ACGGTCTCTCTGTGT	79658
rs11099671	snp	C/T	0.446249	0.154875	intron-variant	ARHGAP10	GRCh38.p7	4:147882641	TCAGTGTCTACATCC[C/T]GTACGTGATGGAGGG	79658
rs11099672	snp	A/G	0.429087	0.174436	intron-variant	ARHGAP10	GRCh38.p7	4:147906822	GAAAAGTTCCCTTCT[A/G]TAACAGGTATTCCAA	79658
rs11099673	snp	A/G	0.428635	0.174898	intron-variant	ARHGAP10	GRCh38.p7	4:147977931	GTTTTCTGTTTCTCC[A/G]TTAGTTCACTTAGGA	79658
rs11099674	snp	A/G	0.499396	0.0173617	intron-variant	ARHGAP10	GRCh38.p7	4:148061765	GCTCCGATGTTGGCT[A/G]ATGGCTCCATGTCCC	79658
rs11099675	snp	C/T	0.420733	0.18262	intron-variant	ARHGAP10	GRCh38.p7	4:148063953	GCAACAAGCCCCTTC[C/T]AGAGCGGTGGCCACC	79658
rs11280645	in-del	-/CCACTGC	0.474813	0.109357	intron-variant	ARHGAP10	GRCh38.p7	4:147911198	TTCTTGAGCAGAAAA[-/CCACTGC]CCACTGCCCAATTCA	79658
rs11281620	in-del	-/TGAG			intron-variant	ARHGAP10	GRCh38.p7	4:148017680	ATATATATATATATA[-/TGAG]TATGTGTGTGTATGT	79658
rs11301771	in-del	-/T	0.5	0	intron-variant	ARHGAP10	GRCh38.p7	4:147761034	TAAGTTAGAGTTAAC[-/T]TTTTTTTTTTTTTTT	79658
rs11309245	in-del	-/T			intron-variant	ARHGAP10	GRCh38.p7	4:148050366	TTACTCATCATCATC[-/T]TTTTTTTTTTTTTTT	79658
rs11311332	in-del	-/T	0.337386	0.23423	intron-variant	ARHGAP10	GRCh38.p7	4:147827179	ATAGTCACTGATCAC[-/T]TTTTTTTTTTTTTAA	79658
rs11325607	in-del	-/C	0.00119737	0.0244387	intron-variant	ARHGAP10	GRCh38.p7	4:147734014	GGAAGTAGGGGGGCG[-/C]CTATACATATGGAGG	79658
rs11339382	in-del	-/A	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147873887	TGAGACCCTGTCTTT[-/A]AAAAAAAAAAAAAGG	79658
rs11348253	in-del	-/T	0.0821764	0.185298	intron-variant	ARHGAP10	GRCh38.p7	4:147815733	GCGTGGTGGTGGTGG[-/T]TTCATGCCTGTAGTC	79658
rs11355244	in-del	-/A	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147756145	CAAAAAAAAAAAAAA[-/A]GAAAAAAAAGAAAGG	79658
rs11363800	in-del	-/A			intron-variant	ARHGAP10	GRCh38.p7	4:148045765	AAAAAAAAAAAAAAA[-/A]GAAATCCATCTAAGA	79658
rs11365271	in-del	-/T	0.197703	0.244469	intron-variant	ARHGAP10	GRCh38.p7	4:147911938	ATTTTTCCTCCTAGG[-/T]TTTTTTTTTTTAAAG	79658
rs11374558	in-del	-/C/T			intron-variant	ARHGAP10	GRCh38.p7	4:147836653	TGGGTTCCTTAAATC[-/C/T]TAAGTACCAAGTAAG	79658
rs11381308	in-del	-/T	0.338976	0.23363	intron-variant	ARHGAP10	GRCh38.p7	4:147828880	GTTTTTTTTTTTTTT[-/T]GAGATGGAGTTTCGT	79658
rs11384854	in-del	-/T			intron-variant	ARHGAP10	GRCh38.p7	4:147878775	TTTCCTTCTTCCTCT[-/T]TTTTTTTTTTTTTTT	79658
rs11393465	in-del	-/A			intron-variant	ARHGAP10	GRCh38.p7	4:148071639	AACAAACAAACAAAC[-/A]AAAAAAAAACACAAA	79658
rs11410393	in-del	-/T	0.403491	0.238422	intron-variant	ARHGAP10	GRCh38.p7	4:147857534	CATAGTTTTTTTTTT[-/T]ATTTGTAGGAAGAAA	79658
rs11419792	in-del	-/T	0.378962	0.21417	intron-variant	ARHGAP10	GRCh38.p7	4:147742904	CTTTTTTTTTTTTTT[-/T]AAAGTTTTGGGGACA	79658
rs11420720	in-del	-/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147742487	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCGC	79658
rs11449935	in-del	-/T	0.394721	0.203852	intron-variant	ARHGAP10	GRCh38.p7	4:147753518	TGGCTAATTTTTTGG[-/T]GTTTTTTTTTTTTTT	79658
rs11457339	in-del	-/A	0.208169	0.246476	intron-variant	ARHGAP10	GRCh38.p7	4:147748384	GGTATAGAAACTAGT[-/A]AAAAAAAAGCTGATG	79658
rs11464640	in-del	-/C	0.0962929	0.197165	intron-variant	ARHGAP10	GRCh38.p7	4:147761896	TTGGACTTTATGTAG[-/C]CAGTAACAGCAGCAA	79658
rs11721640	snp	A/T			intron-variant	ARHGAP10	GRCh38.p7	4:147784818	tataatatattataa[A/T]atatatattataaat	79658
rs11723235	snp	C/T	0.136166	0.22258	intron-variant	ARHGAP10	GRCh38.p7	4:147865674	GCTTTATTAAGATAA[C/T]ATTCACACAGTATAC	79658
rs11724772	snp	C/T	0.0836354	0.186609	intron-variant	ARHGAP10	GRCh38.p7	4:148067644	TAGATGCTCTTGCAG[C/T]GCAATTCCTTTTTGT	79658
rs11724795	snp	A/G	0.452473	0.146644	intron-variant	ARHGAP10	GRCh38.p7	4:147830079	AAGTGTCTTGTCCAC[A/G]GCTGCACCCCTTTCC	79658
rs11725005	snp	A/G	0.149665	0.228982	intron-variant	ARHGAP10	GRCh38.p7	4:147911128	TTTTTTAGAAAACAC[A/G]GTTTTGCTAAGCAGA	79658
rs11725260	snp	C/T	0.371987	0.218218	upstream-variant-2KB	ARHGAP10	GRCh38.p7	4:147730295	CAATATTGAAGAAGT[C/T]TCAGCAGCCCCTCTA	79658
rs11725718	snp	C/T	0.440471	0.161928	intron-variant	ARHGAP10	GRCh38.p7	4:147776114	ATCATTTATGGCCTC[C/T]TCGTAATCATTAACT	79658
rs11725737	snp	C/T	0.001811	0.030037	synonymous-codon, nc-transcript-variant	ARHGAP10	GRCh38.p7	4:148046932	GGACACCCCTACCAG[C/T]AGTCTGGACTCACTT	79658
rs11725869	snp	A/T			intron-variant	ARHGAP10	GRCh38.p7	4:148003268	agtttgcttgcactg[A/T]ggtctgagagatagt	79658
rs11728571	snp	C/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:148051020	GGACCCCAGTAGATC[C/T]GTTGAACAAAAATGC	79658
rs11728928	snp	C/T	0.00953873	0.0683987	intron-variant	ARHGAP10	GRCh38.p7	4:147840316	cagaatgattttttt[C/T]cttctctcatgcagt	79658
rs11729081	snp	C/T	0.434831	0.168337	intron-variant	ARHGAP10	GRCh38.p7	4:147775766	TCCTTTTGCACAGAA[C/T]TATGGTATAAAACAG	79658
rs11730036	snp	G/T	0.435407	0.167703	intron-variant	ARHGAP10	GRCh38.p7	4:147776115	TCATTTATGGCCTCC[G/T]CGTAATCATTAACTT	79658
rs11730620	snp	G/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147912566	atatatatatatata[G/T]atatatatatatata	79658
rs11732086	snp	A/C	0.081446	0.184634	intron-variant	ARHGAP10	GRCh38.p7	4:147975464	gactgggtaattttg[A/C]aggaacagagatttc	79658
rs11733219	snp	C/T	0.495521	0.0471118	intron-variant	ARHGAP10	GRCh38.p7	4:148063958	AAGCCCCTTCTAGAG[C/T]GGTGGCCACCCGGAG	79658
rs11733409	snp	A/G	0.454664	0.143571	intron-variant	ARHGAP10	GRCh38.p7	4:147851530	ATGAATACATTTTAA[A/G]TACAGACTTCCAAAG	79658
rs11733543	snp	A/G	0.118933	0.212888	intron-variant	ARHGAP10	GRCh38.p7	4:147788002	AGTTCCCGGATGTGA[A/G]AAAACTTCGTGAGAA	79658
rs11733794	snp	G/T	0.0524604	0.153226	intron-variant	ARHGAP10	GRCh38.p7	4:147934352	ttgggctccaccaag[G/T]tttcacaaactttta	79658
rs11734553	snp	A/G	0.475702	0.107512	intron-variant	ARHGAP10	GRCh38.p7	4:147906883	TAATTTGGGTTGGGC[A/G]AGCAGCAGTACATAT	79658
rs11734619	snp	A/G	0.484491	0.0866827	intron-variant	ARHGAP10	GRCh38.p7	4:147876939	TCATACAACTACTAA[A/G]TGCTGGAGTTGTCAT	79658
rs11734913	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147789577	atgcccggccCACAT[A/G]TTTTAAATGACATAT	79658
rs11735412	snp	C/T	0.450483	0.149354	intron-variant	ARHGAP10	GRCh38.p7	4:147886700	TATTCATGGGAtcac[C/T]tcaaatacatgacca	79658
rs11737346	snp	C/T	0.477853	0.102875	intron-variant	ARHGAP10	GRCh38.p7	4:147842536	TCTCTAGCCTTGTCT[C/T]GTGATCCTCTCTGAT	79658
rs11737828	snp	C/T	0.112983	0.209108	intron-variant	ARHGAP10	GRCh38.p7	4:147787875	GTGAGGCACCCGACC[C/T]GTGAGGGTTAGAGGG	79658
rs11930432	snp	A/C	0.139564	0.224285	intron-variant	ARHGAP10	GRCh38.p7	4:147779873	AGGTTTAAATGGAAG[A/C]ATGTTGTTTAAAAAT	79658
rs11930900	snp	A/T	0.286825	0.247273	intron-variant	ARHGAP10	GRCh38.p7	4:147915953	TATAAAAATTTTTTT[A/T]AAAAAATTAGCTGAG	79658
rs11930985	snp	A/G	0.00318978	0.0398085	intron-variant	ARHGAP10	GRCh38.p7	4:147916200	CCGTTTCCATGTTCT[A/G]AATATGATTATCTAA	79658
rs11934409	snp	G/T	0.384011	0.216573	intron-variant	ARHGAP10	GRCh38.p7	4:147927734	GGACAGTGCAACTTA[G/T]TGGTGATAGGGGAGC	79658
rs11935450	snp	A/G	0.242775	0.249896	intron-variant	ARHGAP10	GRCh38.p7	4:147811973	CCTTATCAACGAGGC[A/G]GCTGAGCTGGTGACT	79658
rs11935510	snp	C/G	0.217851	0.247924	intron-variant	ARHGAP10	GRCh38.p7	4:147812252	AAAAAAAGAAAACAT[C/G]TCTTTGAAAAATGGG	79658
rs11935620	snp	A/C	0.217851	0.247924	intron-variant	ARHGAP10	GRCh38.p7	4:147812575	TCCCCAGGAGCTGCC[A/C]ATAAAGCCTTTTCCC	79658
rs11937178	snp	A/G	0.335559	0.234904	intron-variant	ARHGAP10	GRCh38.p7	4:147926448	AGGAAAGTGAAAACG[A/G]ACTCTAAGCCTCCCA	79658
rs11938642	snp	A/G	0.110167	0.207236	intron-variant	ARHGAP10	GRCh38.p7	4:147779637	GTTTGGGAGTCTGGG[A/G]AGTGGTGATCACATT	79658
rs11939429	snp	A/G	0.14665	0.227637	intron-variant	ARHGAP10	GRCh38.p7	4:147961086	tggaatttttgggtc[A/G]gtcatagggtatgtg	79658
rs11939997	snp	A/G	0.34303	0.232046	intron-variant	ARHGAP10	GRCh38.p7	4:147921752	TTCACTCATCCCACC[A/G]TTTTACCTCCAGTCC	79658
rs11940379	snp	G/T	0.218151	0.247963	intron-variant	ARHGAP10	GRCh38.p7	4:147812601	TTCCCCACCTCTGCT[G/T]CTTTCTTCTCTTCTA	79658
rs11941546	snp	G/T	0.34146	0.23267	intron-variant	ARHGAP10	GRCh38.p7	4:147917490	GCTTGTATATAGAGG[G/T]TCCCTTCCCACTGTG	79658
rs11942000	snp	C/G	0.183886	0.241099	intron-variant	ARHGAP10	GRCh38.p7	4:148058473	ATCAGGGGCTTGTAT[C/G]TCTAGTGCTGCCCAA	79658
rs11942547	snp	C/T	0.320814	0.239761	intron-variant	ARHGAP10	GRCh38.p7	4:147949640	ACATGAAGGAAAGAG[C/T]AGGTAAGGGATATAA	79658
rs11943897	snp	A/G	0.124144	0.21601	intron-variant	ARHGAP10	GRCh38.p7	4:147864527	AAGAGAAGTCCCTTT[A/G]ATCTTCAGTTCTTGG	79658
rs11943945	snp	C/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147834757	acctgcccccaccct[C/G]acacccatacacacc	79658
rs11944579	snp	A/G	0.236434	0.249632	intron-variant	ARHGAP10	GRCh38.p7	4:147759210	AACTTCCACTTACCA[A/G]TTTTATCTGAGAACT	79658
rs11945312	snp	C/T	0.34303	0.232046	intron-variant	ARHGAP10	GRCh38.p7	4:147920124	ACGTCTTTTAAAAAA[C/T]AACATAACCTCGCTG	79658
rs11945457	snp	A/T	0.381891	0.212379	intron-variant	ARHGAP10	GRCh38.p7	4:147961861	TTCCTGATGACATCG[A/T]ACCTCCCTGGTCCTC	79658
rs11946732	snp	A/G	0.322483	0.239262	intron-variant	ARHGAP10	GRCh38.p7	4:147914379	ttttatttttttaag[A/G]tagggcctcactctg	79658
rs12331287	snp	A/G	0.392325	0.205532	intron-variant	ARHGAP10	GRCh38.p7	4:148035670	GTAACTGAGAATTGG[A/G]CTAAGTGGAATTTTA	79658
rs12331562	snp	A/G	0.286303	0.24735	intron-variant	ARHGAP10	GRCh38.p7	4:147867990	TAAAACCTTATTTTT[A/G]TAATTTATGTGTCAA	79658
rs12332006	snp	G/T	0.00953873	0.0683987	intron-variant	ARHGAP10	GRCh38.p7	4:147792560	TTCCTGTGCTTCTCC[G/T]CACTCCGTCTCTCGG	79658
rs12498257	snp	A/G	0.402277	0.198272	intron-variant	ARHGAP10	GRCh38.p7	4:147855302	TACTTCACAGCATCA[A/G]CTTTTTAAAATAGTG	79658
rs12499150	snp	C/T			intron-variant	ARHGAP10	GRCh38.p7	4:147828044	tcttgaccttgtgat[C/T]tgcccgcctcattca	79658
rs12499404	snp	A/C			intron-variant	ARHGAP10	GRCh38.p7	4:147798781	tctctctctctctct[A/C]tatatatatatatat	79658
rs12499434	snp	C/G	0.5	0	intron-variant	ARHGAP10	GRCh38.p7	4:148069399	TCCAGGGAGGGGAGG[C/G]CTGGGGAGGTGGTGA	79658
rs12508085	snp	C/T	0.283158	0.247791	intron-variant, downstream-variant-500B	ARHGAP10, MIR4799	GRCh38.p7	4:147783145	TTTATATAACACACA[C/T]TAAATTATATATTGT	79658
rs12508143	snp	C/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:148063065	GGAATTAGTGACCTA[C/G]TCATCTGGGATTGGG	79658
rs12508612	snp	C/T	0.0023933	0.0345097	intron-variant	ARHGAP10	GRCh38.p7	4:147993647	CTACAAGGAGCCTGT[C/T]GTTTGCTTTGTTCAA	79658
rs12509618	snp	A/C	0.317784	0.240635	intron-variant	ARHGAP10	GRCh38.p7	4:147906596	AAAAACTTGCCTTTT[A/C]GTGGCCAAGGGGTAA	79658
rs12510691	snp	A/C			intron-variant	ARHGAP10	GRCh38.p7	4:147819737	ctactttttgtattt[A/C]tagtagagatggggt	79658
rs12511313	snp	C/T	0.413914	0.188765	intron-variant	ARHGAP10	GRCh38.p7	4:147860258	CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT	79658
rs12513053	snp	A/T			intron-variant	ARHGAP10	GRCh38.p7	4:147985150	agagggccctgctgc[A/T]ccacagtctctgcac	79658
rs12513192	snp	A/G	0.376989	0.215346	intron-variant	ARHGAP10	GRCh38.p7	4:147897426	TATAATGTTTGATAC[A/G]TATGGGCTTAAATCT	79658
rs12640660	snp	G/T	0.43978	0.162738	intron-variant	ARHGAP10	GRCh38.p7	4:147768726	GTGCTTAAAAATGGG[G/T]GCAAATTTTCTTGTC	79658
rs12641157	snp	G/T	0.420733	0.18262	intron-variant	ARHGAP10	GRCh38.p7	4:148066144	CCTGGGCCTCTGTCT[G/T]GTTTCCCTGGCGGGA	79658
rs12641291	snp	A/C	0.217551	0.247885	intron-variant	ARHGAP10	GRCh38.p7	4:147832792	CTTTTTCTCTTTGTA[A/C]GACATAATATTTTTC	79658
rs12643170	snp	A/G	0.496746	0.040204	intron-variant	ARHGAP10	GRCh38.p7	4:148007221	CTTACTATCTGACAC[A/G]CTTTTCTTTCGGAAA	79658
rs12643550	snp	A/C	0.424037	0.179474	intron-variant	ARHGAP10	GRCh38.p7	4:147907771	TTACACCACCCCCGC[A/C]AAAAACAAAGCATCC	79658
rs12644275	snp	C/G/T	0.00716266	0.059414	intron-variant	ARHGAP10	GRCh38.p7	4:148053970	ATGAAAAGATGACTT[C/G/T]CCAAAATAAAGACAT	79658
rs12645249	snp	C/T	0.434831	0.168337	intron-variant	ARHGAP10	GRCh38.p7	4:147775516	CCTTGCTCTCACATA[C/T]GCAGAATAAGCACCT	79658
rs12646583	snp	C/T	0.499437	0.0167637	intron-variant	ARHGAP10	GRCh38.p7	4:148062053	AGGCGGAGGTGGGAA[C/T]GCCAGGAAGCAGAGC	79658
rs12647314	snp	G/T	0.186421	0.24178	intron-variant	ARHGAP10	GRCh38.p7	4:147832422	GGGAGGCCGAGGTGG[G/T]TGGATCTTGAGGTCA	79658
rs12648074	snp	A/T	0.434831	0.168337	intron-variant	ARHGAP10	GRCh38.p7	4:147775408	GTGTGAGAGGCTGCT[A/T]GGAGAAAGCAATACC	79658
rs12648838	snp	C/T	0.4711	0.116682	intron-variant	ARHGAP10	GRCh38.p7	4:148009964	TTCTGTTCCTTAGAG[C/T]GAATATATACCTTGA	79658
rs12649972	snp	C/T	0.420733	0.18262	intron-variant	ARHGAP10	GRCh38.p7	4:148065910	CAGCTACTGCAGAGG[C/T]TGAGGCAGGAGGATC	79658
rs12650033	snp	A/G	0.420733	0.18262	intron-variant	ARHGAP10	GRCh38.p7	4:148066036	ATAGTAAGTGTGGAA[A/G]TAGGGAGCTCTAATT	79658
rs12650201	snp	C/T	0.174288	0.23826	intron-variant	ARHGAP10	GRCh38.p7	4:147995795	GATCTCTGCTCACTG[C/T]GAGCTTCGCCTCCTG	79658
rs12650219	snp	A/G	0.400147	0.19989	intron-variant	ARHGAP10	GRCh38.p7	4:147820007	AGTTTGGGTGAATGA[A/G]TAAGTGCTATGAAGG	79658
rs12650280	snp	A/G	0.428635	0.174898	intron-variant	ARHGAP10	GRCh38.p7	4:147790150	GTATATTCGGTATCT[A/G]GTGAGGGCCCACTTC	79658
rs13102515	snp	C/G	0.207864	0.246424	intron-variant	ARHGAP10	GRCh38.p7	4:148038402	AAAACTCTCATCCTA[C/G]TGCAACATTTTATAA	79658
rs13103534	snp	A/G	0.478104	0.102316	intron-variant	ARHGAP10	GRCh38.p7	4:148055830	CTGCTGCAGGAAAGC[A/G]CTGGGTATGTGTGGG	79658
rs13104106	snp	A/G	0.4983	0.0291038	intron-variant	ARHGAP10	GRCh38.p7	4:148055865	CCCCAGGCACGAACA[A/G]GGGAGCCCCGCACCA	79658
rs13104594	snp	C/T	0.208779	0.246578	intron-variant	ARHGAP10	GRCh38.p7	4:148019418	GCATTATGGTTCTCA[C/T]TGTGCACATGAGAAA	79658
rs13104796	snp	A/G	0.499325	0.0183582	intron-variant	ARHGAP10	GRCh38.p7	4:148056133	CCTGCCAAGCTTGAA[A/G]TATTTACTCTCTGGC	79658
rs13107848	snp	G/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147912554	aaacaaacaaatata[G/T]atatatatatatata	79658
rs13109093	snp	A/C	0.457504	0.139435	intron-variant	ARHGAP10	GRCh38.p7	4:148061988	GAGCTGAGCCAAGGA[A/C]GGGCAAGATTAGAGC	79658
rs13110489	snp	C/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:148032266	TGATGTTCAtgggtt[C/G]aaccacataaaattg	79658
rs13110502	snp	C/T	0.399073	0.200692	intron-variant	ARHGAP10	GRCh38.p7	4:148025697	TTAGCATATTGAAAA[C/T]TTTACTGCCAGAAGA	79658
rs13110548	snp	A/T	0.499121	0.020948	intron-variant	ARHGAP10	GRCh38.p7	4:148060643	CATCTCCATAGACAC[A/T]GTCTCCAGCCTTGCA	79658
rs13111299	snp	C/T	0.178144	0.239451	intron-variant	ARHGAP10	GRCh38.p7	4:148029261	AGGCACATATATCCA[C/T]GTTCATCCATAGGCT	79658
rs13114883	snp	A/C			intron-variant	ARHGAP10	GRCh38.p7	4:147922587	tagctacttgggagg[A/C]tgaggcaggagaatg	79658
rs13115943	snp	G/T	0.398894	0.200825	intron-variant	ARHGAP10	GRCh38.p7	4:148025864	TGTTAATCTAGTTTG[G/T]GTTAAAATATGCATT	79658
rs13115978	snp	A/G	0.167158	0.235875	intron-variant	ARHGAP10	GRCh38.p7	4:147769097	AATGAATTATGCAGC[A/G]TGATTTCATTATTGC	79658
rs13116821	snp	A/G	0.288386	0.247035	intron-variant	ARHGAP10	GRCh38.p7	4:147829423	CAAACTCCTGACCTC[A/G]GGTGATCCACCCGCC	79658
rs13116955	snp	C/T	0.428484	0.175052	intron-variant	ARHGAP10	GRCh38.p7	4:147790417	CTTTAAAAAATGGGC[C/T]GTCTGGCAGAAAGTA	79658
rs13117046	snp	A/G	0.00358779	0.0422022	intron-variant	ARHGAP10	GRCh38.p7	4:147739284	TTTTTGATTCACAAA[A/G]ATTTGAAGATAAAGT	79658
rs13119069	snp	C/T			intron-variant	ARHGAP10	GRCh38.p7	4:147757279	ggctcactgcaacct[C/T]tgcctcccgtgttca	79658
rs13119246	snp	A/C	0.427423	0.176128	intron-variant	ARHGAP10	GRCh38.p7	4:147905466	ggccagccagttttc[A/C]cagcaccatttatta	79658
rs13119636	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147757320	ctgcctcagcctccc[A/G]aaagctgggactaca	79658
rs13119642	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147757324	ctcagcctcccgaaa[A/G]ctgggactacaggcg	79658
rs13120485	snp	A/G	0.475789	0.107327	intron-variant	ARHGAP10	GRCh38.p7	4:147905759	aagtagttttttcca[A/G]ttctgtgaagaaagt	79658
rs13121312	snp	C/T			intron-variant	ARHGAP10	GRCh38.p7	4:147853875	CTCTTTCAATCCATC[C/T]GGAATTAATTTTGAT	79658
rs13123544	snp	G/T	0.0360663	0.129354	intron-variant	ARHGAP10	GRCh38.p7	4:147878966	tagtagagatggagt[G/T]tcaccgtgttagcca	79658
rs13124167	snp	C/T	0.0766824	0.180169	intron-variant	ARHGAP10	GRCh38.p7	4:147754042	TGTTCCAGGTTCCAG[C/T]AAACTCCTGGCTTAC	79658
rs13127241	snp	A/G	0.263535	0.249633	intron-variant	ARHGAP10	GRCh38.p7	4:148052080	ACACCACAGTAAACT[A/G]TGAATGATTTGCCTA	79658
rs13129325	snp	C/G	0.33875	0.233717	intron-variant	ARHGAP10	GRCh38.p7	4:147864275	AGGGGATCAGACGTT[C/G]TGAGGGCCGCAGATG	79658
rs13129747	snp	C/T	0.21725	0.247846	intron-variant	ARHGAP10	GRCh38.p7	4:147834376	tgggaggctgaggtg[C/T]gaggattgcttgagc	79658
rs13129809	snp	G/T	0.496999	0.0386216	intron-variant	ARHGAP10	GRCh38.p7	4:147982237	ttttataggtaacat[G/T]atccttttctgtagc	79658
rs13130620	snp	C/G			intron-variant	ARHGAP10	GRCh38.p7	4:147834747	acacccacccacctg[C/G]ccccaccctcacacc	79658
rs13133966	snp	A/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147955959	ATTTTTTGTGAGTCA[A/T]ACTCATTTGAGGCTT	79658
rs13134018	snp	A/T	0.437965	0.164831	intron-variant	ARHGAP10	GRCh38.p7	4:147773092	GCTTTAGTTTTTTCT[A/T]TGTTGGTAGAAGGGA	79658
rs13134395	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147789476	tttgtatttttagta[A/G]agatagggtttcact	79658
rs13136202	snp	C/T	0.375399	0.216275	intron-variant	ARHGAP10	GRCh38.p7	4:147777214	TCTTTGCTAATTGAA[C/T]TAGAGTCTGTGTGGC	79658
rs13136624	snp	A/G	0.427271	0.176281	intron-variant	ARHGAP10	GRCh38.p7	4:147777282	TTTTTTTTTTTAGAC[A/G]GAGTCTCACTCTGTC	79658
rs13136858	snp	A/G	0.427271	0.176281	intron-variant	ARHGAP10	GRCh38.p7	4:147777352	CAAGCTCCACCTCCC[A/G]GGTTCACGCCATTCT	79658
rs13136878	snp	A/C			intron-variant	ARHGAP10	GRCh38.p7	4:147895514	tgagaccctgtctca[A/C]aaaaaaaaaaaaaaa	79658
rs13138808	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147860156	AATTGAAAATAACAG[A/G]AGAAggccgggcgtg	79658
rs13138995	snp	A/G	0.495483	0.0473088	intron-variant	ARHGAP10	GRCh38.p7	4:148066279	CTTCCTAGTTTACCC[A/G]TCCTCACATCCCAGT	79658
rs13139509	snp	C/T	0.089084	0.191327	intron-variant	ARHGAP10	GRCh38.p7	4:147969394	ATCCTGTCAAACTGT[C/T]ATTAAGCCTCATTAG	79658
rs13141506	snp	A/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147936041	CAGGCCGTTTTCACA[A/G]AGGCATGTTTGCTTG	79658
rs13144204	snp	C/T	0.0138799	0.0821421	intron-variant	ARHGAP10	GRCh38.p7	4:147801536	TCCAATTTTAGTATT[C/T]ATCATTTTTTGTAAA	79658
rs13145370	snp	A/C			intron-variant	ARHGAP10	GRCh38.p7	4:147853874	ACTCTTTCAATCCAT[A/C]TGGAATTAATTTTGA	79658
rs13145378	snp	A/C			intron-variant	ARHGAP10	GRCh38.p7	4:147853924	TCTGCTTCCCAGTAA[A/C]CAGTCATGCCAGCAC	79658
rs13146245	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147736119	AACTTAAATTGTCTA[A/G]Ctgtgtgtgtgtgtg	79658
rs13146250	snp	G/T			intron-variant	ARHGAP10	GRCh38.p7	4:147757289	aacctctgcctcccg[G/T]gttcaagcaattccc	79658
rs13147412	snp	A/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147766757	cgtaactatattcat[A/G]catatatattttgag	79658
rs13147854	snp	A/G	0.145978	0.227331	intron-variant	ARHGAP10	GRCh38.p7	4:147879148	TGCTGCGTTTTAGAC[A/G]TTTCCTCTTTAGTAA	79658
rs13148956	snp	A/G	0.455144	0.142885	intron-variant	ARHGAP10	GRCh38.p7	4:147849511	TGTAAACAGCATAAA[A/G]CAGTTTTCACGTGGG	79658
rs13149770	snp	G/T	0.49925	0.0193545	intron-variant	ARHGAP10	GRCh38.p7	4:148055415	TGTTCTCAGCTGGGC[G/T]CGGTGGCATACGCCT	79658
rs13149943	snp	A/C			intron-variant	ARHGAP10	GRCh38.p7	4:147927089	atacccacgctctta[A/C]ccacAGTGAGCATGA	79658
rs13149945	snp	A/C			intron-variant	ARHGAP10	GRCh38.p7	4:147927092	cccacgctcttaacc[A/C]cAGTGAGCATGAGGA	79658
rs13150155	snp	A/C			intron-variant	ARHGAP10	GRCh38.p7	4:147927168	ATGAAGGAAAGAAAA[A/C]CAGAAGACAAGCTGT	79658
rs13151898	snp	C/T	0.379942	0.213577	intron-variant	ARHGAP10	GRCh38.p7	4:147881403	AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA	79658
rs13152535	snp	A/G	0.209693	0.246729	intron-variant	ARHGAP10	GRCh38.p7	4:148043790	TGTATATATATATGT[A/G]TATATATATGCATTC	79658
rs13434396	snp	A/G	0.236434	0.249632	intron-variant	ARHGAP10	GRCh38.p7	4:147855221	GTTTGTGACCTTGCT[A/G]CAGAGTCACAGAGTA	79658
rs13434578	snp	G/T	0.34303	0.232046	intron-variant	ARHGAP10	GRCh38.p7	4:147920463	AATCCAAACAAATCA[G/T]CAAAGTCCCAAAGAA	79658
rs13434821	snp	C/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147982546	cacacccagctaaat[C/T]ttttttttttttttt	79658
rs13434950	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147920297	TGGCGGGTGCCTGTA[A/G]TCCCAGCTGCTTGGG	79658
rs13435037	snp	C/T	0.284471	0.247612	intron-variant	ARHGAP10	GRCh38.p7	4:147984337	CTCTCCAGGCCCCAG[C/T]AGGAGGACGCACTGC	79658
rs13435353	snp	A/G	0.0248432	0.108648	intron-variant	ARHGAP10	GRCh38.p7	4:147922472	AGGCGGGCGGATCAC[A/G]AGGTCAGGAGATCGA	79658
rs13435720	snp	G/T			intron-variant	ARHGAP10	GRCh38.p7	4:147920247	gatagtgaaaccctg[G/T]ctctaccaaaaatac	79658
rs13435747	snp	C/T	0.34303	0.232046	intron-variant	ARHGAP10	GRCh38.p7	4:147921994	ATCTCTGGAAAAAGA[C/T]AATGGGCTTGGCCTT	79658
rs13435876	snp	C/G	0.0174175	0.0916809	intron-variant	ARHGAP10	GRCh38.p7	4:147926844	aaggtcaggttggtg[C/G]aggaacaagaaacaa	79658
rs16998723	snp	A/G	0.0150606	0.0854603	intron-variant	ARHGAP10	GRCh38.p7	4:147752199	AGCCTTTAGTATTAT[A/G]GAAGAGCATGCATTA	79658
rs17023724	snp	A/G	0.02016	0.0983543	intron-variant	ARHGAP10	GRCh38.p7	4:147735853	TTCTTAAAATAACCA[A/G]TGTCTTCTTTAAATG	79658
rs17023732	snp	C/T	0.16976	0.236773	intron-variant	ARHGAP10	GRCh38.p7	4:147737986	CATCTGCTGGGGTTC[C/T]TTTGACCAGCTCCTT	79658
rs17023733	snp	G/T	0.02016	0.0983543	intron-variant	ARHGAP10	GRCh38.p7	4:147739562	CTTGTATTTGCTATG[G/T]TAAATTCACAATAAA	79658
rs17023736	snp	A/T	0.0123036	0.0774623	intron-variant	ARHGAP10	GRCh38.p7	4:147739564	TGTATTTGCTATGGT[A/T]AATTCACAATAAAAG	79658
rs17023744	snp	A/T	0.0209421	0.100162	intron-variant	ARHGAP10	GRCh38.p7	4:147754147	CCATCTGGCTCCTGG[A/T]ATGTTTGAGTTGGAA	79658
rs17023749	snp	C/T	0.00159617	0.0282053	intron-variant	ARHGAP10	GRCh38.p7	4:147754419	GATGAAACTTCAGAA[C/T]GTTAAGACAGGCTTA	79658
rs17023757	snp	C/G	0.103794	0.20279	intron-variant	ARHGAP10	GRCh38.p7	4:147757841	CCAACCTGTCTGTTC[C/G]CTTCCCTGGGATCTG	79658
rs17023761	snp	C/T	0.021333	0.101051	intron-variant	ARHGAP10	GRCh38.p7	4:147757902	CAGAACAGGTGTGCC[C/T]GAGACTGCTACCTCA	79658
rs17023763	snp	A/G	0.11228	0.208646	intron-variant	ARHGAP10	GRCh38.p7	4:147759035	ATCTACTTTTTGTCT[A/G]TTTTCTTCAATGCAA	79658
rs17023769	snp	A/G	0.0154538	0.0865337	intron-variant	ARHGAP10	GRCh38.p7	4:147760906	AGACTTGGGCAAACT[A/G]TGTGTATTGGAACAA	79658
rs17023770	snp	A/G	0.221439	0.248363	intron-variant	ARHGAP10	GRCh38.p7	4:147762349	GGTATGCCACAAATT[A/G]ATGTTATTTCTAACT	79658
rs17023771	snp	C/T	0.0718919	0.175435	intron-variant	ARHGAP10	GRCh38.p7	4:147762926	TTATCTACTCTGGAT[C/T]CCATTTGCTAGGGGT	79658
rs17023827	snp	A/G	0.0142736	0.0832652	intron-variant	ARHGAP10	GRCh38.p7	4:147778126	CTGCTAGAAGTGTCG[A/G]TTTAGCGCTGAGAGG	79658
rs17023831	snp	C/T	0.0209421	0.100162	intron-variant	ARHGAP10	GRCh38.p7	4:147778758	TCTGTTTGTAATCTC[C/T]TTTGCAGTGTTATCC	79658
rs17023836	snp	C/T	0.0839998	0.186933	intron-variant	ARHGAP10	GRCh38.p7	4:147798253	GGCAGCCCAAAATAT[C/T]GGTACCTGCCTCTGA	79658
rs17023841	snp	A/T	0.160609	0.233472	intron-variant	ARHGAP10	GRCh38.p7	4:147805857	CTTACTCATGTAATA[A/T]TGCATACAGTGTGGA	79658
rs17023844	snp	A/G	0.272241	0.249009	intron-variant	ARHGAP10	GRCh38.p7	4:147806103	AGAACTACCATGCAC[A/G]CATACTGACGGAGCT	79658
rs17023845	snp	G/T	0.225893	0.248835	intron-variant	ARHGAP10	GRCh38.p7	4:147806204	GTCCAGAGTCCAGGC[G/T]GCTTTCCAGGTCGGA	79658
rs17023846	snp	A/G	0.249038	0.249998	intron-variant	ARHGAP10	GRCh38.p7	4:147807119	CATGAGTTAGGAATT[A/G]GAGAGACCTGGCTTT	79658
rs17023870	snp	A/G	0.218151	0.247963	intron-variant	ARHGAP10	GRCh38.p7	4:147813828	AACTTAACAGCAGCT[A/G]TATAGCATATGTAGT	79658
rs17023889	snp	A/G/T	0.0433465	0.140692	intron-variant	ARHGAP10	GRCh38.p7	4:147816780	GTAAAACAGGAAAAC[A/G/T]TGAAGGAAAATATGA	79658
rs17023896	snp	C/G	0.0752113	0.178743	intron-variant	ARHGAP10	GRCh38.p7	4:147817299	TTAAGGGGTTATCCT[C/G]CACTGACAGTGCTGC	79658
rs17023919	snp	C/G	0.185472	0.241529	intron-variant	ARHGAP10	GRCh38.p7	4:147827207	TAAAGTGGAATCACT[C/G]TGGCTACCTTTGTTT	79658
rs17023928	snp	A/G	0.264358	0.249587	intron-variant	ARHGAP10	GRCh38.p7	4:147830891	TATTACTAAAAGAAT[A/G]TATGATGGTTAAAAT	79658
rs17023931	snp	A/T	0.00358779	0.0422022	intron-variant	ARHGAP10	GRCh38.p7	4:147831325	GCTGGTTTGTGTTAA[A/T]GGAATAGGTTTAGTA	79658
rs17023933	snp	A/C	0.0345262	0.126772	intron-variant	ARHGAP10	GRCh38.p7	4:147831905	GCAAGGCCTTGCCCC[A/C]TGACTCAGTGTCCTC	79658
rs17023942	snp	A/G	0.0376037	0.131863	intron-variant	ARHGAP10	GRCh38.p7	4:147832691	CTCATTGAGGGTGGA[A/G]TTTCTACATCACTAA	79658
rs17023948	snp	A/G	0.021333	0.101051	intron-variant	ARHGAP10	GRCh38.p7	4:147833807	TAGATTCAATGATAT[A/G]TATATTAAGTTGGTG	79658
rs17023950	snp	A/G	0.0633504	0.166319	intron-variant	ARHGAP10	GRCh38.p7	4:147835196	AGTGCTCAGCTAGTG[A/G]CCGCCTGGTAGAGAA	79658
rs17023955	snp	C/T	0.0391387	0.134304	intron-variant	ARHGAP10	GRCh38.p7	4:147836226	GACTTTGGTGATACA[C/T]TGACCTTTTTTTTTA	79658
rs17023959	snp	A/C	0.0633504	0.166319	intron-variant	ARHGAP10	GRCh38.p7	4:147838307	TTGGACAGTCTCTTT[A/C]AAAAACTTATTCCTG	79658
rs17023988	snp	C/T	0.0414363	0.137845	intron-variant	ARHGAP10	GRCh38.p7	4:147843462	TGCCATGGATATTGC[C/T]GAGCTCTCATTCTTT	79658
rs17023992	snp	G/T	0.0349115	0.127424	intron-variant	ARHGAP10	GRCh38.p7	4:147847767	GGGATTCAAAGGTGA[G/T]TGAACCACAGACTTT	79658
rs17023995	snp	A/G	0.233235	0.249437	intron-variant	ARHGAP10	GRCh38.p7	4:147847826	ATTTCCAGGAATAAT[A/G]CAGTGGTTTTGCCAC	79658
rs17024031	snp	C/T	0.0788843	0.182262	intron-variant	ARHGAP10	GRCh38.p7	4:147879961	AAGAAGAGTGATCTA[C/T]GATAAATTTTACTGT	79658
rs17024037	snp	C/T	0.214234	0.247428	intron-variant	ARHGAP10	GRCh38.p7	4:147881950	AAGTTATTGGAATTA[C/T]TGGACATGGTGAAAG	79658
rs17024045	snp	A/G	0.140919	0.224948	intron-variant	ARHGAP10	GRCh38.p7	4:147883444	AGCATACATCTGTGC[A/G]CACACACCCATGGGT	79658
rs17024085	snp	A/G	0.040671	0.13668	intron-variant	ARHGAP10	GRCh38.p7	4:147888048	TCCCTGACATTGCCC[A/G]TCACTCTCTCCTCCA	79658
rs17024101	snp	A/G	0.0655868	0.168795	intron-variant	ARHGAP10	GRCh38.p7	4:147901252	CGTTTTATTTTTCCT[A/G]CACTAATACTTTAGA	79658
rs17024108	snp	A/G	0.02016	0.0983543	intron-variant	ARHGAP10	GRCh38.p7	4:147901429	ATGAGTTAATTCTCA[A/G]TAGTGGAACTGTTTT	79658
rs17024109	snp	A/G	0.0614824	0.164198	intron-variant	ARHGAP10	GRCh38.p7	4:147901458	TTGAGTTATCATTAC[A/G]TTATTTGCCAAAATA	79658
rs17024113	snp	C/T	0.0655868	0.168795	intron-variant	ARHGAP10	GRCh38.p7	4:147901963	TCCTTAGGCTCATGG[C/T]CGACTTTGAGAGTGT	79658
rs17024137	snp	A/C	0.310386	0.242597	intron-variant	ARHGAP10	GRCh38.p7	4:147917868	TTTATTAAACCAGTC[A/C]TTTATTCAAAATGAT	79658
rs17024143	snp	A/G	0.334871	0.235153	intron-variant	ARHGAP10	GRCh38.p7	4:147922767	AGTGAGTCTTTGCAC[A/G]TAGTAGATATTCATT	79658
rs17024163	snp	C/T	0.0696718	0.173152	intron-variant	ARHGAP10	GRCh38.p7	4:147936683	AAGGTGTGTCTCTGA[C/T]GCTGTGACTCCTTAG	79658
rs17024182	snp	A/C	0.164219	0.234823	intron-variant	ARHGAP10	GRCh38.p7	4:147951341	ATATTTTGAAACAAA[A/C]CCCCTAAAGACTTAC	79658
rs17024193	snp	A/G	0.15665	0.231917	intron-variant	ARHGAP10	GRCh38.p7	4:147955828	ATCTAAATTACAGAC[A/G]GAAGGAATATTATGA	79658
rs17024201	snp	C/T	0.093777	0.195178	intron-variant	ARHGAP10	GRCh38.p7	4:147958432	TACCACAAAGGTCTT[C/T]GGTTATTTATCATGA	79658
rs17024210	snp	C/T	0.0174175	0.0916809	intron-variant	ARHGAP10	GRCh38.p7	4:147962298	TTCTGCTTCTTCCAT[C/T]GTAGCGCTCAAATAA	79658
rs17024212	snp	A/G	0.335788	0.23482	intron-variant	ARHGAP10	GRCh38.p7	4:147964719	GAACAGACATGAAAC[A/G]CAGCATGTCAGAAGG	79658
rs17024215	snp	C/T	0.00641136	0.0562545	synonymous-codon, nc-transcript-variant	ARHGAP10	GRCh38.p7	4:147965034	GGAAGAAAGCGGCAG[C/T]CCAGAATCTCGTGTT	79658
rs17024220	snp	C/T	0.182614	0.240747	intron-variant	ARHGAP10	GRCh38.p7	4:147966163	AAAAGTATAATATTC[C/T]GGGGAAAGAGTGAGT	79658
rs17024223	snp	A/G	0.252983	0.249982	intron-variant	ARHGAP10	GRCh38.p7	4:147967340	TGCACCTGGGAAACC[A/G]CCTGCCTTGCAAAGA	79658
rs17024226	snp	C/G	0.26078	0.249767	intron-variant	ARHGAP10	GRCh38.p7	4:147968560	GTAGGTTAAGTATTT[C/G]TGGTTTAAAATGAAT	79658
rs17024235	snp	C/T	0.256619	0.249912	intron-variant	ARHGAP10	GRCh38.p7	4:147969876	TGAATGCACAACCAA[C/T]GTTAATTAAGTGCTC	79658
rs17024236	snp	A/T	0.0955749	0.196603	intron-variant	ARHGAP10	GRCh38.p7	4:147973077	GACATTTCTGTTGAG[A/T]GCCAGAGTGTGGATC	79658
rs17024245	snp	A/G	0.0923359	0.194016	intron-variant	ARHGAP10	GRCh38.p7	4:147994593	AGAAACTCAAAATGT[A/G]GATCGTAATCTCAAT	79658
rs17024251	snp	C/G	0.268995	0.249277	intron-variant	ARHGAP10	GRCh38.p7	4:147996282	AAACAGAAAGGCAGT[C/G]GAAAACAAAACATCA	79658
rs17024280	snp	A/G	0.185788	0.241613	intron-variant	ARHGAP10	GRCh38.p7	4:148009691	TTCCAGATGGTCACC[A/G]TTTTTTAAGTAATCA	79658
rs17024286	snp	A/C	0.00517822	0.0506191	intron-variant	ARHGAP10	GRCh38.p7	4:148052157	TGAAGTCTGGTGCCT[A/C]CTGAGAAATTACAGG	79658
rs17024291	snp	C/T	0.0236746	0.106192	intron-variant	ARHGAP10	GRCh38.p7	4:148057322	GTTATGATTGTGCCT[C/T]CTGAATATCCCGGTA	79658
rs17024294	snp	C/G	0.0494327	0.149241	intron-variant	ARHGAP10	GRCh38.p7	4:148058198	TTCTAGACTTATGCT[C/G]TATGTTTCCCAGACT	79658
rs17024314	snp	C/G	0.0577344	0.159793	intron-variant	ARHGAP10	GRCh38.p7	4:148062912	AGGTTGGACAGATTG[C/G]AGAACCTGGAGAAGG	79658
rs17024317	snp	C/T	0.0252325	0.109451	intron-variant	ARHGAP10	GRCh38.p7	4:148064879	GTCCTTTAAATGCTT[C/T]GGGTTTACCAACTCT	79658
rs17024320	snp	A/G	0.0456336	0.143994	intron-variant	ARHGAP10	GRCh38.p7	4:148068226	AGGTGGTTTCCAGGA[A/G]CGACCCCACGTGGCA	79658
rs17024327	snp	A/G	0.0134861	0.0810011	intron-variant	ARHGAP10	GRCh38.p7	4:148070999	ATTTATGAACAGTCC[A/G]TTGTGCCAGGCACCA	79658
rs17475681	snp	C/T	0.067446	0.170804	intron-variant	ARHGAP10	GRCh38.p7	4:147778877	GACCAGTAAAGAGTT[C/T]ATGGTGGAAGGACTT	79658
rs17475814	snp	C/G	0.0501905	0.150254	intron-variant	ARHGAP10	GRCh38.p7	4:147813553	TGAGGACAGGCCTGC[C/G]AGGCAGTGACATGGC	79658
rs17476057	snp	C/G	0.101658	0.201233	intron-variant	ARHGAP10	GRCh38.p7	4:147899050	AGAGTAGGTGGATTA[C/G]GACACAGAGTAGCCC	79658
rs17476223	snp	A/G	0.0263992	0.111815	intron-variant	ARHGAP10	GRCh38.p7	4:147955811	CATAGACAGATACTC[A/G]GATCTAAATTACAGA	79658
rs17476251	snp	A/G	0.0659589	0.169201	intron-variant	ARHGAP10	GRCh38.p7	4:147961999	TTTCTGTAGAAGTTC[A/G]GCAGCTTTGTCCATG	79658
rs17476412	snp	A/C	0.0858192	0.188533	intron-variant	ARHGAP10	GRCh38.p7	4:147996576	TCAGGGGAGTGAACA[A/C]AGCTTGAAGTGTGTT	79658
rs17579029	snp	A/C	0.104149	0.203046	intron-variant	ARHGAP10	GRCh38.p7	4:147765368	AGTGTGTGTATTTCA[A/C]TGTGCCACGCCCATT	79658
rs17579683	snp	C/G	0.0663309	0.169604	intron-variant	ARHGAP10	GRCh38.p7	4:147963032	GTTCTTTTTCCTATT[C/G]TAATCCATCCTTTAA	79658
rs17579697	snp	C/T	0.0267878	0.112589	intron-variant	ARHGAP10	GRCh38.p7	4:147963465	TTGTCACTTCTTTGA[C/T]GCCTGTGAAAACTAG	79658
rs17613895	snp	A/C	0.138886	0.22395	intron-variant	ARHGAP10	GRCh38.p7	4:147836315	CCAGAAGTTGTCAGA[A/C]TTTCAGCCTTAATCC	79658
rs17613979	snp	G/T	0.235854	0.249599	intron-variant	ARHGAP10	GRCh38.p7	4:147877774	TGTTCTGGGGCATAC[G/T]TGGACAGTCACTCCT	79658
rs17614013	snp	C/T	0.0770498	0.180522	intron-variant	ARHGAP10	GRCh38.p7	4:147889089	TTGTACTGGATTAAA[C/T]GAAATTGAATTGTTG	79658
rs17614025	snp	A/G	0.476574	0.105661	intron-variant	ARHGAP10	GRCh38.p7	4:147889109	TTGAATTGTTGCTCA[A/G]AAGTGACTGAACTGT	79658
rs17676080	snp	C/T	0.248471	0.249995	intron-variant	ARHGAP10	GRCh38.p7	4:147893877	TATAGGTCTCTGTGT[C/T]TTTCATAGAATGTAA	79658
rs17676286	snp	A/G	0.0722614	0.17581	intron-variant	ARHGAP10	GRCh38.p7	4:148007568	TCAAGCCCTTCATGC[A/G]GTGTGTGAACCTCTT	79658
rs28371967	snp	A/G	0.141258	0.225111	intron-variant	ARHGAP10	GRCh38.p7	4:148052676	TAGTGCCTTCTTGTG[A/G]AAGGATGTGGTCTCT	79658
rs28375864	snp	C/T	0.0138799	0.0821421	intron-variant	ARHGAP10	GRCh38.p7	4:147994841	ATGGGGGGAAATGAC[C/T]GCTAAGAGGATTAGT	79658
rs28378383	snp	G/T			intron-variant	ARHGAP10	GRCh38.p7	4:147959244	GAGTATTTTTTTTTT[G/T]GTTTTTGAAGAAGAG	79658
rs28393597	snp	C/T	0.02016	0.0983543	intron-variant	ARHGAP10	GRCh38.p7	4:147918190	GCCTAGGCTGGAGTG[C/T]AGTGGCTTGATCTCG	79658
rs28410093	snp	C/G	0.206336	0.246157	intron-variant	ARHGAP10	GRCh38.p7	4:147977243	CCAGGAACAACAAGA[C/G]TACTTGGAAGGGAAG	79658
rs28410156	snp	A/C	0.413083	0.189483	intron-variant	ARHGAP10	GRCh38.p7	4:148028022	TACGGTTTTTCCTTT[A/C]AAGGAGCTAATTTTC	79658
rs28416885	snp	A/G	0.0558544	0.157504	intron-variant	ARHGAP10	GRCh38.p7	4:147754646	TGTCTTTCACCAGCT[A/G]GAGAATTTGGGTGAA	79658
rs28418775	snp	A/G	0.227664	0.249	intron-variant	ARHGAP10	GRCh38.p7	4:148033158	TTTATAGTATATCTT[A/G]TGTTGCTTTTTATGT	79658
rs28433838	snp	C/G	0.030278	0.119257	upstream-variant-2KB	ARHGAP10	GRCh38.p7	4:147731999	GAGCGCGGGCCCGGC[C/G]GGGTGGCGCCTCGGG	79658
rs28438925	snp	C/T	0.0150606	0.0854603	intron-variant	ARHGAP10	GRCh38.p7	4:147766044	CCAGCACTTTGGTAG[C/T]CTGAGGCCGGTGGAT	79658
rs28445432	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147783187	AACACATTAAATTAT[A/G]TATTGTATAATTTAT	79658
rs28449206	snp	C/G	0.000399281	0.0141238	intron-variant	ARHGAP10	GRCh38.p7	4:147815478	GGCCGGAGGCGGGGG[C/G]CGGGGGGAGGAGGTT	79658
rs28449211	snp	G/T			intron-variant	ARHGAP10	GRCh38.p7	4:147783482	ATTGTATAATTTATA[G/T]AGCACACATTAAATT	79658
rs28454186	snp	G/T	0.0166325	0.0896639	intron-variant	ARHGAP10	GRCh38.p7	4:147771827	AGATGGAGTCTTGCC[G/T]TGTCACCAGGCTGTA	79658
rs28489636	snp	A/G			intron-variant, downstream-variant-500B	ARHGAP10, MIR4799	GRCh38.p7	4:147783124	GTTAAATTATATATT[A/G]TATAATTTATATAAC	79658
rs28493775	snp	A/G	0.266273	0.24947	intron-variant	ARHGAP10	GRCh38.p7	4:147996109	AGAAGTAGGTGCAGG[A/G]GATGGTTTGGGCAGC	79658
rs28496289	snp	C/G	0.0126979	0.078662	intron-variant	ARHGAP10	GRCh38.p7	4:147918220	GGCTCACTGCAAGCT[C/G]TGTCTCCTGGGTTCA	79658
rs28504565	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147783309	TGTATAATTTATATA[A/G]CACACATTAAATTAT	79658
rs28505256	snp	A/G	0.0126979	0.078662	intron-variant	ARHGAP10	GRCh38.p7	4:147918678	GCACAGACCTATCAC[A/G]GCAGCTGTGAGGTTG	79658
rs28505821	snp	A/T	0.430285	0.173197	intron-variant	ARHGAP10	GRCh38.p7	4:147743039	TTTTTTTTTTTTTTT[A/T]AATTTTTATTTTTGG	79658
rs28510261	snp	C/T	0.00795532	0.062565	intron-variant	ARHGAP10	GRCh38.p7	4:147765154	AAATCTAGGAGTCCA[C/T]GCTATTTTCAGTTTT	79658
rs28510990	snp	G/T			intron-variant	ARHGAP10	GRCh38.p7	4:147868243	TGTTGAGTTTTTTTT[G/T]TTTTTTTTTTTGAGA	79658
rs28519574	snp	A/G	0.0126979	0.078662	intron-variant	ARHGAP10	GRCh38.p7	4:148011791	AATTAACTGTAATCT[A/G]TCAGGAGACACCCTG	79658
rs28522552	snp	C/T	0.0652144	0.168387	intron-variant	ARHGAP10	GRCh38.p7	4:147964446	ACATGCCATGCCTTC[C/T]GTTTCTAGGGCTCTG	79658
rs28529145	snp	C/T	0.0221141	0.102801	intron-variant	ARHGAP10	GRCh38.p7	4:147974633	GACCTTAGCTTTGTG[C/T]GGTACTTCAGTGTGC	79658
rs28544401	snp	A/G	0.0126979	0.078662	intron-variant	ARHGAP10	GRCh38.p7	4:148045920	CTCTATGTGTGTCAC[A/G]TTTGCTTCCATAGCA	79658
rs28552498	snp	A/G	0.270892	0.249126	intron-variant	ARHGAP10	GRCh38.p7	4:147996213	GAGAATAGCTAGGAT[A/G]TGGCCTATGGAAACC	79658
rs28558145	snp	C/T	0.169435	0.236663	intron-variant	ARHGAP10	GRCh38.p7	4:148023993	CCGAGCCATGCTGTT[C/T]AGCTAATCGTTGCCA	79658
rs28562228	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147783484	TGTATAATTTATATA[A/G]CACACATTAAATTAT	79658
rs28562405	snp	G/T			intron-variant	ARHGAP10	GRCh38.p7	4:147868244	GTTGAGTTTTTTTTG[G/T]TTTTTTTTTTGAGAC	79658
rs28564360	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:148012368	ACCTTTTAAGGTGCA[A/G]GAGCGAGGTAAAGAT	79658
rs28565935	snp	C/T	0.0123036	0.0774623	intron-variant	ARHGAP10	GRCh38.p7	4:147935214	AGATGAGGTGAGGCC[C/T]GTCATGGATGTGTGC	79658
rs28572262	snp	C/T	0.0333695	0.124785	intron-variant	ARHGAP10	GRCh38.p7	4:148066861	CTGAGTTGCTATAGA[C/T]GTATGGGGGAGAGGC	79658
rs28572267	snp	C/G	0.120674	0.21395	intron-variant	ARHGAP10	GRCh38.p7	4:147959198	TGTCAAAACAAGATA[C/G]AGAAAAAAATGGTTT	79658
rs28575863	snp	A/G	0.0966517	0.197444	intron-variant	ARHGAP10	GRCh38.p7	4:148058556	CTGGTGATTGGTGCA[A/G]CTGGTGTCGAGTTTT	79658
rs28576385	snp	A/T	0.25214	0.249991	intron-variant	ARHGAP10	GRCh38.p7	4:147886429	CCTCCGCAATCCTGA[A/T]TGCAAGACTTTCTCT	79658
rs28579791	snp	A/G	0.0566069	0.158427	intron-variant	ARHGAP10	GRCh38.p7	4:147746349	CCTTGTGATCCGCCC[A/G]CCTTGGCCTCCCAAA	79658
rs28584905	snp	C/T	0.0166325	0.0896639	intron-variant	ARHGAP10	GRCh38.p7	4:147885713	TTAACCATTCTGGTT[C/T]TCCCTCAGATCTCTT	79658
rs28586940	snp	C/G	0.000798403	0.0199641	intron-variant	ARHGAP10	GRCh38.p7	4:147795826	CAGCCTCCCGAATAG[C/G]TGGGATTATAAGTGT	79658
rs28592193	snp	A/T	0.0205511	0.0992634	intron-variant	ARHGAP10	GRCh38.p7	4:147990174	CAACCTCATTATCTC[A/T]TTTGAATTCTTACGA	79658
rs28593418	snp	G/T			intron-variant	ARHGAP10	GRCh38.p7	4:148049824	TTTGTTTGTTTGTTT[G/T]TTTTGGGTGGGGGGG	79658
rs28594565	snp	C/T	0.0652144	0.168387	intron-variant	ARHGAP10	GRCh38.p7	4:147964306	TAAACCAGCCGGTCC[C/T]CAACCTGCGCACCCT	79658
rs28601838	snp	A/G	0.0150606	0.0854603	intron-variant	ARHGAP10	GRCh38.p7	4:147797647	CGATCTCTTGACCTC[A/G]TGATCTGCCCGCCTC	79658
rs28607979	snp	C/T	0.210909	0.246925	intron-variant	ARHGAP10	GRCh38.p7	4:147982052	TTTTTAGTCTTTTTT[C/T]AAAAGACAGGGTTTT	79658
rs28614116	snp	G/T	0.380138	0.213458	intron-variant	ARHGAP10	GRCh38.p7	4:147881492	AAAATACAAAAATCA[G/T]CCAGGTGTGGTGGTG	79658
rs28615270	snp	A/G	0.0126979	0.078662	intron-variant	ARHGAP10	GRCh38.p7	4:148010955	ATGCCTTCTTAGTCT[A/G]CTTTAACTTAGAATA	79658
rs28620191	snp	C/T	0.227369	0.248974	intron-variant	ARHGAP10	GRCh38.p7	4:148033618	CATATACACACATAC[C/T]GCATACATTTATATG	79658
rs28633738	snp	A/G	0.0138799	0.0821421	intron-variant	ARHGAP10	GRCh38.p7	4:147996080	TGTGTGAAATACTCA[A/G]AAAGCTCTTCTTTAG	79658
rs28637907	snp	C/T	0.0652144	0.168387	intron-variant	ARHGAP10	GRCh38.p7	4:147963332	TTCAGGACCCAATCT[C/T]CAAGGGCTCTCCATT	79658
rs28648970	snp	A/G	0.00159617	0.0282053	intron-variant	ARHGAP10	GRCh38.p7	4:147762013	ATTCCCTCTTTTTTT[A/G]TTTTTATTTTTTGAG	79658
rs28662484	snp	C/T	0.239902	0.249796	intron-variant	ARHGAP10	GRCh38.p7	4:147843803	ACAGGCGTGAGCCAC[C/T]GCACCCGGCCTGAAC	79658
rs28664243	snp	A/T	0.0138799	0.0821421	intron-variant	ARHGAP10	GRCh38.p7	4:147917858	TAAAGTCGCATTTAT[A/T]AAACCAGTCCTTTAT	79658
rs28667516	snp	A/C	0.0154538	0.0865337	intron-variant	ARHGAP10	GRCh38.p7	4:147798496	TGGGTGGATCACTTG[A/C]GTCCAGGAGTTTGTG	79658
rs28668372	snp	C/T	0.0670745	0.170406	intron-variant	ARHGAP10	GRCh38.p7	4:147778392	TGGGACATAACTTAC[C/T]GAGATCTGCCATGAC	79658
rs28669164	snp	A/T			intron-variant	ARHGAP10	GRCh38.p7	4:147871808	TAAAAATGGTACATT[A/T]AAAAAATAGTGGCTG	79658
rs28670162	snp	C/G/T	0.000798403	0.0199641	intron-variant	ARHGAP10	GRCh38.p7	4:147967679	CTATGGCTACTCTTA[C/G/T]GATACAACAGAAGAG	79658
rs28670998	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147783858	AACACACATTAAATT[A/G]TGTATTATATTTATA	79658
rs28671664	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147783733	AGAACACATTAAATT[A/G]TGTATTGTATAATTT	79658
rs28681245	snp	C/T	0.0126979	0.078662	intron-variant	ARHGAP10	GRCh38.p7	4:147949981	TGGTTCCTTATTGCC[C/T]CTGGTCTTGTGTTGC	79658
rs28687202	snp	C/T	0.0142736	0.0832652	intron-variant	ARHGAP10	GRCh38.p7	4:147956349	GTGAGGTCCTTGCTC[C/T]AGCCAGTGTAAAGGT	79658
rs28711870	snp	A/G	0.00358779	0.0422022	intron-variant	ARHGAP10	GRCh38.p7	4:147783533	AACACACATTAAATT[A/G]TGTATTGTATAATTT	79658
rs28716209	snp	A/G	0.0490535	0.14873	intron-variant	ARHGAP10	GRCh38.p7	4:147967717	CTTGCAACAGAGACC[A/G]GATAGCCCGCAAGGC	79658
rs28720862	snp	C/G	0.0138799	0.0821421	intron-variant	ARHGAP10	GRCh38.p7	4:147991999	GTGCAGGATTAACTT[C/G]AGTGTGGAGCCTGGG	79658
rs28725304	snp	C/T	0.396	0.202938	intron-variant	ARHGAP10	GRCh38.p7	4:147967513	GACCCAGGTGATCCA[C/T]GTTGGGGTGAGCAGA	79658
rs28726377	snp	A/T	0.0592355	0.161582	intron-variant	ARHGAP10	GRCh38.p7	4:147766129	TTACTGGAAAAAAAA[A/T]AAATAAATAAATTAG	79658
rs28739356	snp	G/T			intron-variant	ARHGAP10	GRCh38.p7	4:147959208	AGATAGAGAAAAAAA[G/T]GGTTTTATTTAAAAA	79658
rs28754310	snp	G/T			intron-variant	ARHGAP10	GRCh38.p7	4:147912552	ACAAACAAACAAATA[G/T]ATATATATATATATA	79658
rs28754881	snp	C/T	0.261608	0.24973	intron-variant	ARHGAP10	GRCh38.p7	4:148002763	TCAGTGGTGATATCC[C/T]CTTTATCATTTTTTA	79658
rs28759001	snp	C/T	0.0256215	0.110247	intron-variant	ARHGAP10	GRCh38.p7	4:148058447	TGCATTCAGTGCTTA[C/T]ACAGGCTGGAATCAG	79658
rs28888171	snp	A/G	0.0146672	0.084371	intron-variant	ARHGAP10	GRCh38.p7	4:148002563	TTTTTTTGGTTGGTA[A/G]GCTATTAATTATTGC	79658
rs33932101	in-del	-/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147911644	GGGATTACAGGCGTG[-/G]AGCCACCGCGCCTGG	79658
rs33932988	in-del	-/A	0.288127	0.247076	intron-variant	ARHGAP10	GRCh38.p7	4:147869583	AATGACAGTTTATTG[-/A]AAAAAAAAAAGCCTT	79658
rs33937677	in-del	-/C	0.029116	0.117091	intron-variant	ARHGAP10	GRCh38.p7	4:147914557	CGCATGTTCTGCGCT[-/C]CCCCCCCCCCCTTTT	79658
rs33943951	in-del	-/G	0.148661	0.22854	intron-variant	ARHGAP10	GRCh38.p7	4:147894141	TTGCATAAATACTTT[-/G]GGTGTGGGAATTGCT	79658
rs33957234	in-del	-/T	0.354665	0.227036	intron-variant	ARHGAP10	GRCh38.p7	4:147951404	CTGTGGTATAGTTGA[-/T]TTTTTTTTTTTTTTC	79658
rs33957928	in-del	-/A	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147880909	ATAAATTTTTACACT[-/A]AAAAAAAGAGTACAA	79658
rs33975020	in-del	-/C	0.097727	0.198275	intron-variant	ARHGAP10	GRCh38.p7	4:147891957	CACTTTGTGCTGTGA[-/C]CCCCCCACACATTTG	79658
rs33978656	in-del	-/T	0.128632	0.218563	intron-variant	ARHGAP10	GRCh38.p7	4:147914592	TTAACATCTTCAGCA[-/T]TTTTTGTACAAATGG	79658
rs34017910	in-del	-/T			intron-variant	ARHGAP10	GRCh38.p7	4:147796371	TGTGAGCATTTTTTT[-/T]AAAAGCGTAGTGGAA	79658
rs34033252	in-del	-/T			intron-variant	ARHGAP10	GRCh38.p7	4:148020568	TTTTATTCCTGCATT[-/T]AGTGTGCTGAGGATA	79658
rs34034984	in-del	-/G			intron-variant	ARHGAP10	GRCh38.p7	4:148052877	TTAAATTCTGCACAG[-/G]AGGTTAGCTCCTTCC	79658
rs34040830	in-del	-/G			intron-variant	ARHGAP10	GRCh38.p7	4:147896878	TATTTTTTAAAAATT[-/G]CCAAATGGCTGGAGA	79658
rs34042816	snp	A/C			intron-variant	ARHGAP10	GRCh38.p7	4:147914921	ACTTTGGAGATACTA[A/C]ATATTAAACATTGCA	79658
rs34048442	in-del	-/G			intron-variant	ARHGAP10	GRCh38.p7	4:147879843	TCCTTTTTATGCCAC[-/G]TGTTTGGAAGATAAA	79658
rs34051206	snp	C/T			missense, nc-transcript-variant	ARHGAP10	GRCh38.p7	4:147966712	AGCAGAACCTGATGA[C/T]TGTGGCAAACTTAGG	79658
rs34061522	in-del	-/A	0.121022	0.21416	intron-variant	ARHGAP10	GRCh38.p7	4:147780560	AAGAAGGAGACTAGG[-/A]AAAAAAAGACTGAAC	79658
rs34083575	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147954192	GTGGAGTGTCATTTA[A/G]GTGAAGGACATGCCA	79658
rs34085253	in-del	-/TTT			intron-variant	ARHGAP10	GRCh38.p7	4:147870575	TAAAAGTGGCTAGAC[-/TTT]TTTTTTTTTTTTGAG	79658
rs34107652	snp	A/C			intron-variant	ARHGAP10	GRCh38.p7	4:147914981	TCTTTGTTTAGCGAT[A/C]TAGTGAAGTATGTAT	79658
rs34121160	in-del	-/T			intron-variant	ARHGAP10	GRCh38.p7	4:147761055	AGAGTCTTGCTCTGT[-/T]GCCCAGGCTGGAGTG	79658
rs34147989	in-del	-/T			intron-variant	ARHGAP10	GRCh38.p7	4:147752808	CGGGATTACAGGCGT[-/T]GAGCTGCCGCACCTG	79658
rs34156818	in-del	-/G			intron-variant	ARHGAP10	GRCh38.p7	4:147901114	TGCTATTGATTTTGG[-/G]CAGTTTGAAATGTGT	79658
rs34158761	snp	C/T	0.00517822	0.0506191	intron-variant	ARHGAP10	GRCh38.p7	4:148069704	AAGTGCTAGTAACCC[C/T]GTATTGCAGGTAACA	79658
rs34159946	snp	A/G/T			intron-variant	ARHGAP10	GRCh38.p7	4:147924676	GGTACACTGTTAGCA[A/G/T]AGTGGTGAAGAACAT	79658
rs34163684	in-del	-/TA			intron-variant	ARHGAP10	GRCh38.p7	4:147833811	TCAATGATATATATA[-/TA]TTAAGTTGGTGGTAG	79658
rs34167588	in-del	-/T			intron-variant	ARHGAP10	GRCh38.p7	4:147970245	GTTAGCCACGGGTTT[-/T]CCCTGGCAGCTGACC	79658
rs34169210	in-del	-/A	0.499087	0.0213463	intron-variant	ARHGAP10	GRCh38.p7	4:147922708	AAAAAAAAAAAAAAA[-/A]TTTTATTCATACTAC	79658
rs34189452	in-del	-/A			intron-variant	ARHGAP10	GRCh38.p7	4:147965542	CTCCTCCTTTTAAAA[-/A]CCGGCAAAATCAAAT	79658
rs34193686	in-del	-/T	0.0494327	0.149241	intron-variant	ARHGAP10	GRCh38.p7	4:147793321	ATATATATATATATA[-/T]TTTTTTTTTTTTACA	79658
rs34195889	snp	G/T			intron-variant	ARHGAP10	GRCh38.p7	4:147949518	GCTCCTGGCATCTGG[G/T]GGCATCTGACATCCT	79658
rs34210939	in-del	-/C			intron-variant	ARHGAP10	GRCh38.p7	4:147984941	CACCTACAGGTCCCC[-/C]AATGGCAGGTCCGAG	79658
rs34216395	in-del	-/C	0.079617	0.182947	intron-variant	ARHGAP10	GRCh38.p7	4:147868350	CAAGTACTCCTCCTG[-/C]CTCAGCCTCCTGAGT	79658
rs34261824	in-del	-/G			intron-variant	ARHGAP10	GRCh38.p7	4:147775801	ATGCAGCACATCTGG[-/G]ATAGTGGCAGGCTCT	79658
rs34262495	in-del	-/T	0.138207	0.223612	intron-variant	ARHGAP10	GRCh38.p7	4:147870563	TAAAAGTGGCTAGAC[-/T]TTTTTTTTTTTTTTG	79658
rs34287232	snp	C/T	0.465473	0.126772	intron-variant	ARHGAP10	GRCh38.p7	4:147911651	ACAGGCGTGAGCCAC[C/T]GCGCCTGGCCTCTTA	79658
rs34301274	in-del	-/A			intron-variant	ARHGAP10	GRCh38.p7	4:148008900	GCTGTCTACTGTTAA[-/A]GTCGGACGTTAAAGA	79658
rs34310368	snp	A/C			intron-variant	ARHGAP10	GRCh38.p7	4:147932829	TAAAAAATGGAAAAA[A/C]CAATAAAAAGGTAAT	79658
rs34313322	snp	A/G	0.0107246	0.0724382	intron-variant	ARHGAP10	GRCh38.p7	4:148043778	TGTGTATATATATGT[A/G]TATATATATGTATAT	79658
rs34329766	snp	C/T			intron-variant	ARHGAP10	GRCh38.p7	4:147763696	ACCCTGCAGGTAATT[C/T]TAACATGTAGTCAGG	79658
rs34340295	in-del	-/T	0.499502	0.0157669	intron-variant	ARHGAP10	GRCh38.p7	4:147851256	GACTATGACTAATAA[-/T]TTTTTTTTTTTTTTA	79658
rs34348974	in-del	-/T			intron-variant	ARHGAP10	GRCh38.p7	4:147826543	AGCCAACCACGGAAT[-/T]AACAGGACACCTCCT	79658
rs34349553	in-del	-/T/TG/TGT/TGTGT	0.0821764	0.185298	intron-variant	ARHGAP10	GRCh38.p7	4:147765338	GTGTGTGTGTGTGTG[-/T/TG/TGT/TGTGT]GGGGGGGGGGTGTGA	79658
rs34350231	snp	C/G			intron-variant	ARHGAP10	GRCh38.p7	4:147942812	TTCCCCTCTGGGAGC[C/G]TAAGGCAGCTATCCG	79658
rs34359270	in-del	-/C			intron-variant	ARHGAP10	GRCh38.p7	4:147748503	TTCCTAAGAGGGTAG[-/C]ATCTTATATTAAGTG	79658
rs34366141	snp	C/T			intron-variant	ARHGAP10	GRCh38.p7	4:147970835	GCTCATGCCTGTAAT[C/T]TCAGCACTTCGGGAG	79658
rs34367322	in-del	-/G			intron-variant	ARHGAP10	GRCh38.p7	4:147755805	GTGAGTGGTTGTGGG[-/G]TGTGTGTGTGTAGTG	79658
rs34371108	in-del	-/G			intron-variant	ARHGAP10	GRCh38.p7	4:148035866	AATCTGGACTTTTTT[-/G]CTAGCAGTAATCATG	79658
rs34375248	in-del	-/T	0.39009	0.207062	intron-variant	ARHGAP10	GRCh38.p7	4:147859289	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTTTTGC	79658
rs34376866	in-del	-/T			intron-variant	ARHGAP10	GRCh38.p7	4:147947479	CGATCTTGGCTCACT[-/T]GCAACCTCTGCCTCC	79658
rs34381026	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147914917	GCAGACTTTGGAGAT[A/G]CTAAATATTAAACAT	79658
rs34385454	in-del	-/T			intron-variant	ARHGAP10	GRCh38.p7	4:147871139	TAATTTTTGTATTTT[-/T]AGTAGAGACGGGGTT	79658
rs34388709	in-del	-/T	0.429538	0.173972	intron-variant	ARHGAP10	GRCh38.p7	4:147768742	GCAAATTTTCTTGTC[-/T]TTTTTTTTTTTTTTG	79658
rs34406157	in-del	-/A			intron-variant	ARHGAP10	GRCh38.p7	4:147934250	TTGGAGGACTGGACC[-/A]TTGTCAAGCTTGAAT	79658
rs34430977	in-del	-/C			intron-variant	ARHGAP10	GRCh38.p7	4:147879643	TGATTTGCTGCACCC[-/C]ATCAACCCATCATCT	79658
rs34439178	snp	C/G			intron-variant	ARHGAP10	GRCh38.p7	4:147915028	TCACTCTCATATATT[C/G]TGTATTCCAGTCCGA	79658
rs34461241	snp	C/T			intron-variant, upstream-variant-2KB	ARHGAP10, MIR4799	GRCh38.p7	4:147781772	TCTTTATTAATTGCA[C/T]ACAATTACTAATCTA	79658
rs34467040	in-del	-/T	0.453697	0.14494	intron-variant	ARHGAP10	GRCh38.p7	4:147838546	GATTTCTCTTCCTCC[-/T]CTTCTTCTTCACAGG	79658
rs34471617	in-del	-/T			intron-variant	ARHGAP10	GRCh38.p7	4:147961080	TACGAGTGGAATTTT[-/T]GGGTCGGTCATAGGG	79658
rs34471913	snp	C/G	0.00953873	0.0683987	intron-variant	ARHGAP10	GRCh38.p7	4:147882154	AGTCATTCTAACCAG[C/G]GTTGTCACTTAAAAA	79658
rs34473616	in-del	-/AC			intron-variant	ARHGAP10	GRCh38.p7	4:147783812	TATTATATTTATATA[-/AC]ACACATTAAATTGTG	79658
rs34482147	in-del	-/T			intron-variant	ARHGAP10	GRCh38.p7	4:148013867	AGGAAGACTCTTTTT[-/T]ATCAGGGTTCTCACT	79658
rs34501731	in-del	-/T			intron-variant	ARHGAP10	GRCh38.p7	4:147839822	CTTTCCTTTCCTTTT[-/T]AGACATTTAAGATCC	79658
rs34527033	in-del	-/CT			intron-variant	ARHGAP10	GRCh38.p7	4:148014770	TCTGCTATGCATCAC[-/CT]TATTTAGCGTATAGA	79658
rs34530294	in-del	-/A			intron-variant	ARHGAP10	GRCh38.p7	4:147943206	GAAATTGTGAGAAAA[-/A]TGTGGTAGTAGTTTG	79658
rs34540456	in-del	-/A			intron-variant	ARHGAP10	GRCh38.p7	4:147734468	CTTTTTTTCTCGTTA[-/A]TGTTCATTAAGAATT	79658
rs34551897	in-del	-/AAAA	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:148065993	AAAAAAAAAAAAAAA[-/AAAA]GGGTTGAGGGGATTA	79658
rs34560317	in-del	-/T	0.333722	0.235565	intron-variant	ARHGAP10	GRCh38.p7	4:147924972	TTGAAGAACTTTCTA[-/T]TTTTTTTTTTTTAAA	79658
rs34563874	in-del	-/C			intron-variant	ARHGAP10	GRCh38.p7	4:147815862	AGAGTGAGACAGTCC[-/C]TGCTGACACCTTGAT	79658
rs34566906	in-del	-/T			intron-variant	ARHGAP10	GRCh38.p7	4:147933234	AATTGTTTATTTTTT[-/T]AGGGACAAGGTTTTG	79658
rs34580209	snp	C/T	0.370568	0.219005	intron-variant	ARHGAP10	GRCh38.p7	4:148049386	TGCTTCTCTGAGGAG[C/T]GTAATTAGGATAAGT	79658
rs34581344	in-del	-/TG			intron-variant	ARHGAP10	GRCh38.p7	4:147736121	CTTAAATTGTCTAGC[-/TG]TGTGTGTGTGTGTGT	79658
rs34582085	in-del	-/G			intron-variant	ARHGAP10	GRCh38.p7	4:147753303	TCCTGTCAGTTCAGG[-/G]AAGCTCATTTCTAGT	79658
rs34594079	in-del	-/G			intron-variant	ARHGAP10	GRCh38.p7	4:147911961	TTTAAAGGATTGTGT[-/G]TCTTAGATTCTCAAG	79658
rs34602025	in-del	-/C			intron-variant	ARHGAP10	GRCh38.p7	4:147935811	ACGTGAGATTTCCAA[-/C]GCTGCTTTTGTGCAA	79658
rs34609304	in-del	-/C			intron-variant	ARHGAP10	GRCh38.p7	4:147840636	TTATGTTAAACTTTC[-/C]AGTTAAGAGAACATT	79658
rs34639507	in-del	-/C			intron-variant	ARHGAP10	GRCh38.p7	4:148000440	TTTGTGTACATACCC[-/C]AGTAATGGGATGGCT	79658
rs34646235	in-del	-/T			intron-variant	ARHGAP10	GRCh38.p7	4:147741174	TACCTATGCATTTTT[-/T]GGATGATAAAACTAA	79658
rs34658756	snp	C/G			intron-variant	ARHGAP10	GRCh38.p7	4:147919212	TAGTGTATAACATAT[C/G]TTAAATAACAAATAA	79658
rs34660452	in-del	-/A			intron-variant	ARHGAP10	GRCh38.p7	4:147869593	ATTGAAAAAAAAAAA[-/A]GCCTTTTTTGTATTC	79658
rs34675866	snp	A/G	0.5	0	intron-variant	ARHGAP10	GRCh38.p7	4:147865570	AAGGATATTTCATGT[A/G]GATTTCAGCAAAAAA	79658
rs34690971	in-del	-/T	0.424968	0.178567	intron-variant	ARHGAP10	GRCh38.p7	4:148059521	AAAGGACTCTCAAAA[-/T]ATTTCATTATGTTCT	79658
rs34694852	in-del	-/ATAT			intron-variant	ARHGAP10	GRCh38.p7	4:148043753	TATATATGTATATAT[-/ATAT]GTATATATATGTGTA	79658
rs34762040	in-del	-/TAT			intron-variant	ARHGAP10	GRCh38.p7	4:147890299	CATTACTACTTTGAT[-/TAT]CAATGGTTAGATGGA	79658
rs34773133	in-del	-/A			intron-variant	ARHGAP10	GRCh38.p7	4:147758243	ACTGCAGCCTGGGCA[-/A]CAAGAGCGAAACTTC	79658
rs34782915	in-del	-/T			intron-variant	ARHGAP10	GRCh38.p7	4:147947247	TTTTTTTTTTTTTTT[-/T]AAAGAAAAGAACTTA	79658
rs34792193	in-del	-/G			intron-variant	ARHGAP10	GRCh38.p7	4:147864317	TGGCCCGCCTTTGAG[-/G]AGCCGGGTTCTTGAG	79658
rs34806340	in-del	-/A			intron-variant	ARHGAP10	GRCh38.p7	4:147919158	AGACAAATGTCTAAA[-/A]CTGTACTATCGTTCT	79658
rs34807956	snp	C/T			intron-variant	ARHGAP10	GRCh38.p7	4:147942858	CCTCTAAGCCTTTCC[C/T]TGGACCAAGCTTCTT	79658
rs34831712	in-del	-/A			intron-variant	ARHGAP10	GRCh38.p7	4:147962310	ATCGTAGCGCTCAAA[-/A]TAATAATAGTAACAC	79658
rs34833952	in-del	-/A/AA	0.0663353	0.169609	intron-variant	ARHGAP10	GRCh38.p7	4:147910349	TCAAAAAAAAAAAAA[-/A/AA]TTGTACAAAATACTT	79658
rs34854324	in-del	-/A			frameshift-variant, intron-variant, nc-transcript-variant	ARHGAP10	GRCh38.p7	4:148063299	ACAAGCCACCTGAAA[-/A]GGTACGTGGTTTGGA	79658
rs34854334	in-del	-/C	0.351418	0.228505	intron-variant	ARHGAP10	GRCh38.p7	4:147759581	CATAGTGATACACCG[-/C]CCCCCCCCCCCTTTA	79658
rs34876546	in-del	-/TTTTTT			intron-variant	ARHGAP10	GRCh38.p7	4:148039392	TTTTTTTTTTTTTTT[-/TTTTTT]GAGATAGAGTCTCAC	79658
rs34886470	in-del	-/CCACTGC			intron-variant	ARHGAP10	GRCh38.p7	4:147911199	TCTTGAGCAGAAAAC[-/CCACTGC]CACTGCCCAATTCAT	79658
rs34924031	snp	C/T	0.178465	0.239547	intron-variant	ARHGAP10	GRCh38.p7	4:148047880	CAGGGTGGAGTGCAG[C/T]GGTACCATCTTGGTT	79658
rs34957409	snp	A/G	0.274929	0.248754	intron-variant	ARHGAP10	GRCh38.p7	4:148049320	TGAGCCTTGATATGG[A/G]AGACCATCCCCTGCT	79658
rs34963096	in-del	-/T			intron-variant	ARHGAP10	GRCh38.p7	4:147765340	GTGTGTGTGTGTGTG[-/T]GGGGGGGGGTGTGAG	79658
rs34970355	snp	A/G	0.47517	0.10862	intron-variant	ARHGAP10	GRCh38.p7	4:147902073	GGTATATTGTAGTTG[A/G]TCTGTCTTCTATTTG	79658
rs34975734	in-del	-/C			intron-variant	ARHGAP10	GRCh38.p7	4:148014948	TTTTAGTTGTAAACC[-/C]TAAGTTGAAGTTGTT	79658
rs34987220	snp	C/G			intron-variant	ARHGAP10	GRCh38.p7	4:147985978	TCTCCTCTCTGGAGT[C/G]TGGGGTGTCCTTTGC	79658

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