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

RNF111

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs745800	snp	C/G/T	0	0	utr-variant-3-prime	RNF111	GRCh38.p7	15:59095793	GATATCTTAACTTTT[C/G/T]GTGCTTAGCAGAAGA	54778
rs877269	snp	A/T	0.413083	0.189483	intron-variant	RNF111	GRCh38.p7	15:59081595	CTGGGTGAGGCTCAT[A/T]CCCGTAATCCCCAGT	54778
rs935363	snp	C/T	0.159622	0.233092	intron-variant	RNF111	GRCh38.p7	15:59069478	AAGTTGTATACATAA[C/T]TGATGTCTCAAACTA	54778
rs935364	snp	A/G	0.0271762	0.113356	intron-variant	RNF111	GRCh38.p7	15:59010046	CACAAAGCTAAAAAA[A/G]AATTGCATATAAACT	54778
rs1014443	snp	C/T	0.171704	0.237423	intron-variant	RNF111	GRCh38.p7	15:59045598	TGGGCATTACCAATT[C/T]GACATGGAGAAAAGT	54778
rs1044673	snp	A/G	0.124144	0.21601	utr-variant-3-prime	RNF111	GRCh38.p7	15:59097267	AACTAAAATTCTTTT[A/G]TTAGCAAGTCCTTAT	54778
rs1044674	snp	C/T	0	0	utr-variant-3-prime	RNF111	GRCh38.p7	15:59095832	TTGATTTTGTAGACA[C/T]ATTAAGTCAAGATTT	54778
rs1074701	snp	A/G	0.489608	0.0713316	intron-variant	RNF111	GRCh38.p7	15:59073862	tgtatttctttaata[A/G]taagacttgaaagtt	54778
rs1074702	snp	G/T	0.415399	0.187465	intron-variant	RNF111	GRCh38.p7	15:59073900	ctccttgattcatag[G/T]ctgcagactggatgt	54778
rs1345116	snp	A/G	0.471292	0.116318	intron-variant	RNF111	GRCh38.p7	15:59038714	GAAATGATGCCATAT[A/G]TAAAAAAGAATTAAA	54778
rs1374155	snp	C/T	0.426201	0.177351	intron-variant	RNF111	GRCh38.p7	15:59030630	TCTTATAAAACGTTT[C/T]TCTCTGGTCACTCTA	54778
rs1374156	snp	A/G	0.495671	0.0463237	intron-variant	RNF111	GRCh38.p7	15:59046746	tgtcttttgaagcac[A/G]aaagtctctaatttt	54778
rs1446237	snp	A/G	0.424348	0.179172	intron-variant	RNF111	GRCh38.p7	15:59052603	TTTTGGTAAGAGATA[A/G]AATATTGCTATGTTA	54778
rs1446238	snp	A/G	0.424037	0.179474	intron-variant	RNF111	GRCh38.p7	15:59055558	ATGATTTTTAATTAC[A/G]ATTATTTCTTTGGAG	54778
rs1446239	snp	A/C	0.475496	0.107942	synonymous-codon	RNF111	GRCh38.p7	15:59055730	TTGGAGCCAGGGTTC[A/C]AGTTCTCATGCAAGT	54778
rs1446240	snp	A/C	0.42574	0.177808	intron-variant	RNF111	GRCh38.p7	15:59004292	AACAGCAAGTTCCTT[A/C]TGTTGGAGATAATAA	54778
rs1613602	snp	A/C	0.103689	0.203589	intron-variant	RNF111	GRCh38.p7	15:59002418	TATTAGAACATTCTT[A/C]TGTGAGGGACAAGTT	54778
rs1665049	snp	A/G	0.463666	0.129795	intron-variant	RNF111	GRCh38.p7	15:58998453	cccctcattgtgtcc[A/G]tatgttcttgggaag	54778
rs1665050	snp	A/G	0.481087	0.0953875	intron-variant	RNF111	GRCh38.p7	15:59001406	TCTACTTTGCCTGCT[A/G]TTAGTTCCTATTTTT	54778
rs1665051	snp	C/T	0.488786	0.0740357	intron-variant	RNF111	GRCh38.p7	15:59003025	TCATTATGTTGCCAG[C/T]GCGGGATTGCAGTTG	54778
rs1665053	snp	C/T	0.451234	0.14834	intron-variant	RNF111	GRCh38.p7	15:58990275	CGACAAACACAACAA[C/T]GAATACCAAAAACCT	54778
rs1693532	snp	C/T	0.481165	0.0951993	intron-variant	RNF111	GRCh38.p7	15:58993820	AACTAAGATGCTAAT[C/T]GTGTATGCCCTCAGG	54778
rs1693534	snp	A/C	0.461813	0.132798	intron-variant	RNF111	GRCh38.p7	15:58989763	CTGCACCTTAGCTTT[A/C]TACAAGCAAGGTGCT	54778
rs1693535	snp	C/T	0.0283406	0.115616	intron-variant	RNF111	GRCh38.p7	15:58998706	aagtttgaattttat[C/T]ttggcaataaattct	54778
rs1693536	snp	C/T	0.0279526	0.114869	intron-variant	RNF111	GRCh38.p7	15:59004938	TTTTGCTGCTCTCCA[C/T]TGGGTCTCACTTCCC	54778
rs1867757	snp	A/G	0.492533	0.0606443	intron-variant	RNF111	GRCh38.p7	15:59072315	ttctatgggtaaaac[A/G]ccattaaacagcatc	54778
rs1867758	snp	G/T	0.418653	0.184544	intron-variant	RNF111	GRCh38.p7	15:59072270	aatctttcatgaaag[G/T]aacagtcaatcaatg	54778
rs1965171	snp	A/G	0.0592355	0.161582	intron-variant	RNF111	GRCh38.p7	15:59019763	caggaattcgagacc[A/G]gcctggccaacgtgg	54778
rs1968605	snp	G/T	0.0329836	0.124112	intron-variant	RNF111	GRCh38.p7	15:59019818	acaaaaattagccag[G/T]tgtggtggtgtgtgc	54778
rs1968606	snp	C/T	0.424659	0.17887	intron-variant	RNF111	GRCh38.p7	15:59019875	gaggcagcaaaattg[C/T]ttgaacctgggagat	54778
rs1968607	snp	C/T	0.424968	0.178567	intron-variant	RNF111	GRCh38.p7	15:59019925	gatcgtgccactgca[C/T]ttcagcctgggtgac	54778
rs1971181	snp	A/G	0.41023	0.191902	intron-variant	RNF111	GRCh38.p7	15:59069005	CTCACTGCAATCTCC[A/G]CCTCCCACGTTCAAT	54778
rs1975534	snp	C/T	0.416871	0.186156	intron-variant	RNF111	GRCh38.p7	15:59044043	aactctgtctccccc[C/T]accagaaaaaaaaaG	54778
rs2121236	snp	A/G	0.492435	0.0610346	intron-variant	RNF111	GRCh38.p7	15:59091923	TCCTGTCAGATCAGC[A/G]GCAGCGATAGATTCT	54778
rs2121237	snp	C/T	0.444666	0.15686	intron-variant	RNF111	GRCh38.p7	15:59091888	GAAGCGTGAACCCTA[C/T]TGTAAACTGTGCATG	54778
rs2289895	snp	A/T	0.414245	0.188477	intron-variant	RNF111	GRCh38.p7	15:59089570	CTCAATGTTTTCAAT[A/T]CAACTGCTCATAAAA	54778
rs2414618	snp	C/T	0.420892	0.182472	intron-variant	RNF111	GRCh38.p7	15:59019684	AGTATTTAAGCCAGG[C/T]GTGGTGGCTTATGCC	54778
rs2592092	snp	A/C	0.426047	0.177503			GRCh38.p7	15:59003608	ggttttgccgtgttg[A/C]ccaggctggtcttga	54778
rs2874741	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59086159	gagtctcactctgtc[A/G]cccaggctggagtgc	54778
rs2899640	snp	A/G	0.438526	0.164189	intron-variant	RNF111	GRCh38.p7	15:59060281	TATATACAATAACAT[A/G]TAAGATACCCAAGTA	54778
rs2899641	snp	C/T	0.00755907	0.0610114	intron-variant	RNF111	GRCh38.p7	15:59052552	CACTAATCTGATATA[C/T]GCATACTCAAACTGG	54778
rs2899642	snp	C/G	0.464087	0.129169	missense	RNF111	GRCh38.p7	15:59030849	GACTCCTGAATATAA[C/G]GAGCTCTACACCTTA	54778
rs2935478	snp	C/T	0.303438	0.244222	intron-variant	RNF111	GRCh38.p7	15:58990648	GACAGAGCGAGACTG[C/T]TTCTCAAAACAAACA	54778
rs2955703	snp	C/T	0.0275645	0.114116	intron-variant	RNF111	GRCh38.p7	15:59003384	ttatgggattacagg[C/T]gtgagccgccacacc	54778
rs2955704	snp	A/G	0.498982	0.0225409	intron-variant	RNF111	GRCh38.p7	15:58990372	AAAACCTGTCATGAA[A/G]CTGTGGGCCAGGCGT	54778
rs3052989	in-del	-/AAT	0.373196	0.217538	intron-variant	RNF111	GRCh38.p7	15:59060785	aataataataataat[-/AAT]GCTACATAAAGCTAC	54778
rs3052991	in-del	-/TA	0.420415	0.182917	intron-variant	RNF111	GRCh38.p7	15:59023535	AGTGTTATTTTTATT[-/TA]TATATTTTTGGTAAA	54778
rs3751539	snp	A/G	0.0166325	0.0896639	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096014	TAATTTGTGCCTCAC[A/G]GTATCTGCAGATTTA	54778
rs3809531	snp	G/T	0.210301	0.246828	intron-variant	RNF111	GRCh38.p7	15:59085254	CTTGGTTGTTGACAT[G/T]AAGGACGATTAGAAT	54778
rs3809532	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59085126	ATGTTCTGCCTCAAA[A/C]GTCATTGTGGTTCAA	54778
rs4145892	snp	C/T	0.00597247	0.0543191	utr-variant-3-prime	RNF111	GRCh38.p7	15:59095278	AAGCCTTGATAATTA[C/T]GAATTTTTTATCCAT	54778
rs4531678	snp	G/T	0.377385	0.215112	intron-variant	RNF111	GRCh38.p7	15:58995754	CAGGCATGAGATGCC[G/T]TGCCCCGGCCTTTTT	54778
rs4531679	snp	A/G	0.492679	0.0600586	intron-variant	RNF111	GRCh38.p7	15:59083246	GTAAACTGGGATGCA[A/G]AATAAAGAGTATGAA	54778
rs4774320	snp	C/T	0.436408	0.16659	intron-variant	RNF111	GRCh38.p7	15:59033234	TAGTCTACTTTTGGA[C/T]GTGCCATTTCTTCTT	54778
rs4774321	snp	C/T	0.462582	0.131564	intron-variant	RNF111	GRCh38.p7	15:59033264	TCTCTTCTTCTTCTT[C/T]ATGAGTCCCTTTCTT	54778
rs4775110	snp	C/G	0.439224	0.163383	intron-variant	RNF111	GRCh38.p7	15:59023685	CCCTTGTTTAAATGA[C/G]TTTACTAGCCTTTCC	54778
rs4775111	snp	C/T	0.44768	0.153045	intron-variant	RNF111	GRCh38.p7	15:59033591	AGCTCAGTTTGTGCT[C/T]GAAGTCAGTGAGACA	54778
rs4775112	snp	A/G	0.0329836	0.124112	intron-variant	RNF111	GRCh38.p7	15:59034356	AAAATGTTGTTGGCT[A/G]TTGTTACCAGAATGC	54778
rs4775114	snp	A/G	0.427727	0.175821	intron-variant	RNF111	GRCh38.p7	15:59059635	CCGTTGCCTAATCCA[A/G]GGTCACAAAAATTTA	54778
rs4775115	snp	G/T	0.433527	0.169758	intron-variant	RNF111	GRCh38.p7	15:59076311	TCCCAGTTCTTAAAT[G/T]TTTAGTATTTACTTG	54778
rs5812958	in-del	-/T	0.0659589	0.169201	intron-variant	RNF111	GRCh38.p7	15:59019547	TGTTTTTCATATGGG[-/T]TTATACACCATTCTT	54778
rs5812960	in-del	-/T	0.49681	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59045168	ACAGTTTTTTTTTTT[-/T]AAGTGTTTCCTCTTT	54778
rs5812961	in-del	-/A/ATT			intron-variant	RNF111	GRCh38.p7	15:59060809	ATTATTATTATTATT[-/A/ATT]TTTTTTTTTGTGAGA	54778
rs6145580	in-del	-/GTTCTTGTCAGGCT			intron-variant	RNF111	GRCh38.p7	15:59019570	CATTCTTGTCAGGCT[-/GTTCTTGTCAGGCT]TAATACCTTGGAATA	54778
rs6145581	in-del	-/AGTTGGTGATTCATTCAGCAA	0.493293	0.0575177	intron-variant	RNF111	GRCh38.p7	15:59055523	ATTCTTAGGTCAATT[-/AGTTGGTGATTCATTCAGCAA]AGTTTACCGAGTGCC	54778
rs6494052	snp	A/G	0.0648419	0.167978	intron-variant	RNF111	GRCh38.p7	15:59003726	AATAGCACGTGTTTC[A/G]CTCTAAAATTATCTT	54778
rs6494054	snp	A/G	0.497881	0.0324789	intron-variant	RNF111	GRCh38.p7	15:59014581	AGAAAGCTTCAGAAG[A/G]AATGTATACTTGTTT	54778
rs6494058	snp	C/T	0.0637235	0.166737	intron-variant	RNF111	GRCh38.p7	15:59035203	ccacctggccctgtc[C/T]atgacacgtgggaat	54778
rs6494064	snp	C/T	0.495596	0.0467178	intron-variant	RNF111	GRCh38.p7	15:59053192	TCTGAACTAACACAT[C/T]AATGAAACATCCTTA	54778
rs6494065	snp	A/G	0.493293	0.0575177	intron-variant	RNF111	GRCh38.p7	15:59053249	ACATTGCCCTATTGC[A/G]GAATCACTTTGACTC	54778
rs6494066	snp	A/G	0.201418	0.245234	intron-variant	RNF111	GRCh38.p7	15:59059622	catatctaagaaacc[A/G]ttgcctaatccaggg	54778
rs6494067	snp	C/G	0.0930568	0.194599	intron-variant	RNF111	GRCh38.p7	15:59067809	TTCCCCTTTTACCTC[C/G]TACTGTAGAGTTCAC	54778
rs6494069	snp	C/T	0.491936	0.0629843	intron-variant	RNF111	GRCh38.p7	15:59094151	ACATCTCCTTTTAAC[C/T]TACCTGTTAAACAGT	54778
rs7163736	snp	A/G	0.138886	0.22395	intron-variant	RNF111	GRCh38.p7	15:59034341	AGGGTATATGCATTG[A/G]AAATGTTGTTGGCTG	54778
rs7164061	snp	A/G	0.0637235	0.166737	intron-variant	RNF111	GRCh38.p7	15:59034271	CAACATTGTGCTTGC[A/G]TTTTATACACCTATG	54778
rs7164205	snp	C/T	0.0115144	0.0749975	intron-variant	RNF111	GRCh38.p7	15:59056171	AAAGTAGAAGCAGTA[C/T]TTTTTAAATATAAAC	54778
rs7165028	snp	A/T	0.489318	0.0722982	intron-variant	RNF111	GRCh38.p7	15:59078703	GTCTCTACTAAAAAT[A/T]CAAAAACTAGCCGGG	54778
rs7168102	snp	C/G	0.438526	0.164189	intron-variant	RNF111	GRCh38.p7	15:59023115	taactgggcatggtg[C/G]tgcgtgtctgtaatc	54778
rs7169181	snp	A/G	0.35445	0.227135	intron-variant	RNF111	GRCh38.p7	15:59032154	ATGTTGAACAGGCTA[A/G]TCTTGAGCTCCTGAT	54778
rs7170844	snp	A/C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59009201	tgacctcaggtgatc[A/C/T]gcccaccttggcctt	54778
rs7171252	snp	A/G	0.0379877	0.132479	intron-variant	RNF111	GRCh38.p7	15:59050166	gcctcctgagttcca[A/G]cgattttcctgcctc	54778
rs7171621	snp	A/T	0	0	intron-variant	RNF111	GRCh38.p7	15:59007750	taatttgcattcctc[A/T]ggtgactaaagatat	54778
rs7171680	snp	A/G	0.0486741	0.148216	intron-variant	RNF111	GRCh38.p7	15:59016768	cctattaggaactag[A/G]ccatgtaccagtagg	54778
rs7173135	snp	G/T	0.488485	0.0749998	intron-variant	RNF111	GRCh38.p7	15:59016939	AGGGATCTAGGTTGC[G/T]TGCTCCTTACGAGAA	54778
rs7174057	snp	C/T	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59032562	AAGTAGCTGGGACTA[C/T]AGGCCCACACCACCA	54778
rs7175215	snp	C/G	0.484632	0.086302	intron-variant	RNF111	GRCh38.p7	15:59041399	tctctaccaaaaata[C/G]aaaaattagccgggt	54778
rs7175246	snp	A/G	0.491421	0.0649309	intron-variant	RNF111	GRCh38.p7	15:59014054	ccatggcctcccaac[A/G]tgctaggattacagg	54778
rs7175490	snp	C/T	0.487049	0.0794222	intron-variant	RNF111	GRCh38.p7	15:59041735	gtgattgtaaccatt[C/T]tgaatgctcaccggc	54778
rs7176281	snp	A/G	0.468249	0.121932	intron-variant	RNF111	GRCh38.p7	15:59036230	gcccagctaatcttt[A/G]tatttttattagaga	54778
rs7176576	snp	C/T	0.491368	0.0651254	intron-variant	RNF111	GRCh38.p7	15:59013949	acacgccaccacgcc[C/T]ggctaatttttgtat	54778
rs7177112	snp	A/C/G	0.039737	0.135242	intron-variant	RNF111	GRCh38.p7	15:59089648	AAATTGATTTAGCCT[A/C/G]TCTCTTCTGTTGAAA	54778
rs7178935	snp	A/G	0.445773	0.155477	synonymous-codon	RNF111	GRCh38.p7	15:59075968	GCAGGCATTGCCAGT[A/G]GACCTGAGCAACAGT	54778
rs7180666	snp	A/G	0.105569	0.204058	intron-variant	RNF111	GRCh38.p7	15:59072352	tcagaattggaatca[A/G]tcctttcaaactttg	54778
rs7181728	snp	A/C	0.0368353	0.130617	intron-variant	RNF111	GRCh38.p7	15:59081389	gtggcatgcacttgt[A/C]gtcacagctccttgg	54778
rs7181747	snp	A/G	0.136166	0.22258	intron-variant	RNF111	GRCh38.p7	15:59034131	AAGGATAAATAATGT[A/G]GCTCTTTTTATATCA	54778
rs7183794	snp	A/G	0.0275645	0.114116	intron-variant	RNF111	GRCh38.p7	15:59052098	AGAGGAAGTAAACAT[A/G]CAAAGAAGTGTAGAT	54778
rs7183822	snp	A/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59060807	attattattattatt[A/T]tttttttttttgtga	54778
rs8024187	snp	A/G	0.0126979	0.078662	intron-variant	RNF111	GRCh38.p7	15:59006231	taatttatatacaat[A/G]tgaggcacacgtttt	54778
rs8025246	snp	G/T	0.494187	0.0535994	intron-variant	RNF111	GRCh38.p7	15:59025814	CGGCTCACCGCAACC[G/T]CTGCCTTGCGGATTC	54778
rs8025439	snp	C/G	0.0134861	0.0810011	intron-variant	RNF111	GRCh38.p7	15:59025945	atgttggtcaggctg[C/G]tctcgaactcccaac	54778
rs8026611	snp	A/T	0.495708	0.0461266	intron-variant	RNF111	GRCh38.p7	15:59048927	aagatcctgtctctt[A/T]aaaaaacaaacaaac	54778
rs8027536	snp	C/G	0.482309	0.0923707	intron-variant, utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022364	CTGTCTAAATGTAAG[C/G]GTGGTTCCATCTTTG	54778
rs8028752	snp	A/G	0.39325	0.204889	intron-variant	RNF111	GRCh38.p7	15:59003803	ttctatgtcctgttc[A/G]tggctgatgccagtg	54778
rs8028764	snp	C/T	0.492087	0.0623997	intron-variant	RNF111	GRCh38.p7	15:59012436	AGTAGGTTTTCTTTA[C/T]GCTTTATGTCACAAA	54778
rs8029153	snp	C/T	0.432651	0.170701	intron-variant	RNF111	GRCh38.p7	15:59082904	TTTAACAGTCTTATC[C/T]TCCAGTAACTGGCAA	54778
rs8029336	snp	A/C	0.491157	0.065903	intron-variant	RNF111	GRCh38.p7	15:59012889	gattacaggtgcctg[A/C]caccacacctggcta	54778
rs8030246	snp	A/G	0.422	0.181428	intron-variant	RNF111	GRCh38.p7	15:59049447	TTCAGGCTCCTGTCC[A/G]TTGGTTCTCACAAAG	54778
rs8030323	snp	A/G	0.415399	0.187465	intron-variant	RNF111	GRCh38.p7	15:59048048	tagggaaacaatttg[A/G]cagttccttaaaaag	54778
rs8030514	snp	C/T	0.0376037	0.131863	intron-variant	RNF111	GRCh38.p7	15:59056778	GATCTGTAAGACAGT[C/T]GTTAATGTAATAGGG	54778
rs8030811	snp	A/G	0.106633	0.204807	intron-variant	RNF111	GRCh38.p7	15:59065467	TTATCTTTTCTAACA[A/G]CCATGCAaggcaatt	54778
rs8031390	snp	A/G	0.418653	0.184544	intron-variant	RNF111	GRCh38.p7	15:59049811	GGAGTGCAATGGCGC[A/G]ATCTCGGCTCACTGC	54778
rs8032299	snp	A/G	0.0372196	0.131242	intron-variant	RNF111	GRCh38.p7	15:59044630	AACCTTAAAAAAAAA[A/G]CAATTCGAAGAAAAT	54778
rs8035850	snp	C/G	0.197393	0.244402	intron-variant	RNF111	GRCh38.p7	15:59080363	TGGCTTCAGGTGACT[C/G]TGCCCACCTTGGCCT	54778
rs8035952	snp	A/G	0.0652144	0.168387	intron-variant	RNF111	GRCh38.p7	15:59027516	ctgaaaataaaagaa[A/G]ttctatacctttttt	54778
rs8037569	snp	G/T	0.462582	0.131564	intron-variant	RNF111	GRCh38.p7	15:59010263	aattaataaaCCCAT[G/T]ACATGTAAATATAAA	54778
rs8039612	snp	C/T	0.00599995	0.0544424	intron-variant	RNF111	GRCh38.p7	15:59093469	acctacctcagcctc[C/T]caaaatgctgggatt	54778
rs8040456	snp	A/G	0.467845	0.122652	intron-variant	RNF111	GRCh38.p7	15:59063904	GTGAGTGAGCTTAGT[A/G]TCCCAAAGGTTTTCA	54778
rs8040605	snp	A/G	0.0659589	0.169201	intron-variant	RNF111	GRCh38.p7	15:58999059	aagttttggggtagt[A/G]tcaaagaggaataac	54778
rs8040788	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59064133	TGGTCAGTTCCTGAT[A/G]TGCTAGTTTTAACAC	54778
rs8041221	snp	C/T	0.491316	0.0653198	intron-variant	RNF111	GRCh38.p7	15:59042609	tggtgtttatcctta[C/T]gtataataggaaaaa	54778
rs8041704	snp	A/C	0.494057	0.0541878	intron-variant	RNF111	GRCh38.p7	15:59051430	gccactgcactccag[A/C]ctgggcgattgagcg	54778
rs8042516	snp	C/T	0.436692	0.166271	intron-variant	RNF111	GRCh38.p7	15:59067525	AATCACATTCTTACA[C/T]TCGAAAATGGCCTAA	54778
rs8042896	snp	C/T	0.437118	0.165792	intron-variant	RNF111	GRCh38.p7	15:59067727	ATTTTTGGGATCTTA[C/T]TTTAAACAAATTGTT	54778
rs8043536	snp	A/G	0.261884	0.249717	intron-variant	RNF111	GRCh38.p7	15:59046522	GAGTattgtatattc[A/G]tatgcagaaaagata	54778
rs9302206	snp	C/T	0.492966	0.0588865	intron-variant	RNF111	GRCh38.p7	15:59017274	TTAAGTTTGATTTTC[C/T]AGAGATCGTAAATGC	54778
rs9708068	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59009906	ggctgcagtgagctg[G/T]gatcctgccattgtg	54778
rs9788719	snp	C/T	0.428484	0.175052	intron-variant	RNF111	GRCh38.p7	15:59028920	aagtagctgggatta[C/T]agtcagtgcgccact	54778
rs10083611	snp	A/T	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:59003566	accacacccagctaa[A/T]ttttttaaaattttt	54778
rs10431762	snp	A/C	0.410061	0.192043	intron-variant	RNF111	GRCh38.p7	15:59066330	ATATGGCACTATCAG[A/C]CGGGGTGTGGTGGCT	54778
rs10431791	snp	A/G	0.485731	0.0832509	intron-variant	RNF111	GRCh38.p7	15:59055159	TAAACTAGCCACAAT[A/G]TCCTTACCTCTACAC	54778
rs10431792	snp	C/T	0.466618	0.124806	intron-variant	RNF111	GRCh38.p7	15:59066181	GTAATAAATCATTTA[C/T]TGTGCCATAGGAAAA	54778
rs10431793	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59066607	acagcaagactccat[C/T]tcaaaaaaaaaagaa	54778
rs10518995	snp	C/T	0.151668	0.229849	intron-variant	RNF111	GRCh38.p7	15:59003877	TTATTGAATGAGAAC[C/T]ATAAATGAATAAGTG	54778
rs10518996	snp	C/T	0.491834	0.0633738	intron-variant	RNF111	GRCh38.p7	15:59085247	GTTTGCTATTCTAAT[C/T]GTCCTTAATGTCAAC	54778
rs10851642	snp	A/G	0.410399	0.191761	intron-variant	RNF111	GRCh38.p7	15:59077909	TTTTCCTGAAGGAGT[A/G]TGTGTATTCTCTCCC	54778
rs11071404	snp	C/G	0	0	intron-variant	RNF111	GRCh38.p7	15:59014524	TGCTGTGGAATTATA[C/G]AAAGCAGCTTTTCAA	54778
rs11071405	snp	C/T	0.456685	0.140646	intron-variant	RNF111	GRCh38.p7	15:59038867	CAGATGTTGTCATTC[C/T]GATCCTTCCATTATA	54778
rs11281531	in-del	-/AGTTAGT	0.398174	0.201356	intron-variant	RNF111	GRCh38.p7	15:59024462	TAGCAAGATCTTTTC[-/AGTTAGT]AGCAAGTACTTTAAG	54778
rs11281889	in-del	-/TTAGTAG	0	0	intron-variant	RNF111	GRCh38.p7	15:59024464	GCAAGATCTTTTCAG[-/TTAGTAG]CAAGTACTTTAAGAA	54778
rs11337128	in-del	-/A	0.482234	0.0925596	intron-variant	RNF111	GRCh38.p7	15:58997517	TACACATTTGCAGTT[-/A]AAAAAAAAAAAAAAA	54778
rs11394653	in-del	-/T	0.111092	0.207857	intron-variant	RNF111	GRCh38.p7	15:59052284	CTTTAAATGTTTTTT[-/T]CTTTTTGTTTCCAGG	54778
rs11412501	in-del	-/A	0.261608	0.24973	intron-variant	RNF111	GRCh38.p7	15:59046329	CCTGGGTAGCTGGTA[-/A]CTGCAGGCACATGCC	54778
rs11630536	snp	C/T	0.00874735	0.0655527	intron-variant	RNF111	GRCh38.p7	15:59057321	GAAGTTCTTTTCCCC[C/T]TTTTTTATGTACAAG	54778
rs11634263	snp	C/T	0.0832709	0.186283	intron-variant	RNF111	GRCh38.p7	15:59046197	GCttttttttttttt[C/T]ccctttaattttttg	54778
rs11635706	snp	G/T	0	0	intron-variant	RNF111	GRCh38.p7	15:59018980	ccaggttggagtgca[G/T]tggtaagacctcagc	54778
rs11635820	snp	A/G	0.496999	0.0386216	intron-variant	RNF111	GRCh38.p7	15:59016008	GGTGCACCCCACCAC[A/G]CCTAGATAACTTTTG	54778
rs11635958	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59007079	gcTGTTTACAGtttt[A/T]aaagtaaactttaca	54778
rs11636229	snp	C/T	0.00475057	0.0485048	intron-variant	RNF111	GRCh38.p7	15:59061389	TTATCCAAGTTCCTC[C/T]GTAAATTTATGGTTT	54778
rs11636644	snp	A/C/G			intron-variant	RNF111	GRCh38.p7	15:58991523	catgaggaaaaTAGG[A/C/G]CCATGTGATACGGCA	54778
rs11636707	snp	A/G	0.373598	0.21731	intron-variant	RNF111	GRCh38.p7	15:59079464	AAGTTTCCTTTAAGT[A/G]CATGCTAACAAGGCA	54778
rs11852461	snp	A/G	0.480775	0.0961398	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021728	AACTCAGTGATCCCT[A/G]GATCGAAAATCTACA	54778
rs11855063	snp	C/G	0.330947	0.236533	intron-variant	RNF111	GRCh38.p7	15:59029757	GTGGGCTGTAGTAAT[C/G]GGAAGAAGATTTCTA	54778
rs11855536	snp	C/T	0.413914	0.188765	intron-variant	RNF111	GRCh38.p7	15:59042508	TTAGGAATACTTTTA[C/T]CACTCCAAAGTTCTA	54778
rs12050865	snp	A/G	0.420574	0.182769	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020689	AATTGAAACCTATTA[A/G]TTGAGAGAGGTTTAA	54778
rs12101733	snp	A/G	0.493154	0.0581045	intron-variant	RNF111	GRCh38.p7	15:59047566	accattagttatttt[A/G]tgttttttttaatta	54778
rs12381120	snp	G/T	0.211516	0.24702	intron-variant	RNF111	GRCh38.p7	15:58993228	TAATTAGTAAAAGTg[G/T]ccaggtatagtggct	54778
rs12437587	snp	A/T	0.492237	0.0618148	intron-variant	RNF111	GRCh38.p7	15:59072785	cctagtatctttacc[A/T]ggagaagattctatc	54778
rs12438111	snp	C/T	0.450231	0.149691	intron-variant	RNF111	GRCh38.p7	15:59057540	TGGATTTATTCCTAC[C/T]GTTCTCAATTTTAAG	54778
rs12438128	snp	A/G	0.391769	0.205917	intron-variant	RNF111	GRCh38.p7	15:59006943	ggcgcccgctaccac[A/G]cccagctaatttttt	54778
rs12438208	snp	G/T	0.430285	0.173197	intron-variant	RNF111	GRCh38.p7	15:59057715	AAAACATATAAAAAG[G/T]CATGGAAAGGAGATT	54778
rs12438962	snp	A/G	0.410905	0.191336	intron-variant	RNF111	GRCh38.p7	15:59065694	CTATTGGTTCTGACT[A/G]TAGAGTCCAAAGGAA	54778
rs12440692	snp	A/G	0.478932	0.10045	intron-variant	RNF111	GRCh38.p7	15:59090671	ACATAGTACCATGTG[A/G]TAATATTGTTGTAAT	54778
rs12441973	snp	C/T	0.413914	0.188765	intron-variant	RNF111	GRCh38.p7	15:59057016	TTTCTCATTGGAAAG[C/T]TTCTCTCTTATTAAA	54778
rs12442086	snp	A/G	0.419456	0.183806	intron-variant	RNF111	GRCh38.p7	15:59074364	ggctgttttgtcgac[A/G]tggaaaatctgttat	54778
rs12442134	snp	A/C	0.418007	0.185132	intron-variant	RNF111	GRCh38.p7	15:59074478	tccttgcacttttat[A/C]ttatagagatagctt	54778
rs12442301	snp	C/T	0.415399	0.187465	intron-variant	RNF111	GRCh38.p7	15:59065968	ATTTGTGTTGGTGGA[C/T]AGTGAGACTTCACCA	54778
rs12593271	snp	A/G/T	0.444444	0.157135	intron-variant	RNF111	GRCh38.p7	15:58989886	CTTCTTTTTTTTTTT[A/G/T]TTATAGTTTAAAGAG	54778
rs12595746	snp	C/G	0	0	intron-variant	RNF111	GRCh38.p7	15:58998925	gttacaaagtcatgt[C/G]tgggtgaaagatcta	54778
rs12595781	snp	A/T	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:59024811	CTGAAACTCAGTAAC[A/T]GTTAAACACTAACTC	54778
rs12899165	snp	A/G	0.307176	0.243374	intron-variant	RNF111	GRCh38.p7	15:58994102	GAGTGCAGTGGCCCC[A/G]TCTTGGCTCATTGTC	54778
rs12901282	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59078430	catgtagttcctgct[C/T]ttcaggaggctgagg	54778
rs12901391	snp	A/G	0	0	intron-variant	RNF111	GRCh38.p7	15:59078332	AAAACAACTGTACTT[A/G]AAATGCTATTATTTA	54778
rs12901578	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59078551	agtgagaacctgtct[C/T]taaaaaaaaaaaaaa	54778
rs12904061	snp	C/T	0.00557542	0.0525036	intron-variant	RNF111	GRCh38.p7	15:59064980	TTATTTAAGCTGTTT[C/T]GGTTGGATTTTTATT	54778
rs12905422	snp	A/G	0.433963	0.169285	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:58988080	TAAGGTGAGGGGAAC[A/G]GGGGGGGAGGGGATC	54778
rs12906212	snp	A/C	0.40853	0.193309	intron-variant	RNF111	GRCh38.p7	15:59070556	AACCGTATTTACCTG[A/C]ATTGAAGACATACAT	54778
rs12907497	snp	C/T	0.0115144	0.0749975	intron-variant	RNF111	GRCh38.p7	15:59070644	AGGAGAACAGACATA[C/T]ACTTGATTGTAGATA	54778
rs12907548	snp	A/T	0.35207	0.228214	intron-variant	RNF111	GRCh38.p7	15:59026992	GATTTAACCATAAAG[A/T]GTTGATTGCATTGTT	54778
rs12909315	snp	C/T	0	0	intron-variant	RNF111	GRCh38.p7	15:59020033	TGGGGTTAATGGATT[C/T]TTGAGTTTAGTTCTC	54778
rs12909361	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59037634	ctgaggtctggagtt[A/C]gagaccagcctgacc	54778
rs12909819	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59016812	agtagtgaagcttca[C/T]ctatatttacagcca	54778
rs12910349	snp	A/T	0.136847	0.222927	intron-variant	RNF111	GRCh38.p7	15:58996220	AACTATTTTTAACTA[A/T]GTCATCAAACATTCT	54778
rs12910656	snp	A/G	0.0154538	0.0865337	intron-variant	RNF111	GRCh38.p7	15:59038221	TGTGAGGTATGGCAC[A/G]CACTGACTCCATGAG	54778
rs12910879	snp	A/G	0.0322114	0.122752	intron-variant	RNF111	GRCh38.p7	15:59062743	CATATCCAAGGTTAT[A/G]TGATAGTGGAGCAAG	54778
rs12910987	snp	C/T	0.421526	0.181876	intron-variant	RNF111	GRCh38.p7	15:59092782	GAGGCTCTCTTGAGG[C/T]CAGGAGTTTGAGGCC	54778
rs12911336	snp	G/T	0	0	intron-variant	RNF111	GRCh38.p7	15:59092252	AAATAGTTTATATTG[G/T]TTATCATTCTCATTG	54778
rs12912335	snp	A/C	0.140919	0.224948	intron-variant	RNF111	GRCh38.p7	15:58992585	caccttgggaggctg[A/C]ggaaggtggattgct	54778
rs12912429	snp	A/G	0.435694	0.167385	intron-variant	RNF111	GRCh38.p7	15:59071815	GTATTCCTAATAcaa[A/G]cataccttggagata	54778
rs12912440	snp	C/G	0.00597247	0.0543191	intron-variant	RNF111	GRCh38.p7	15:59071836	cttggagatactgca[C/G]gtttggttccagaca	54778
rs12913177	snp	A/G	0.470715	0.117409	intron-variant	RNF111	GRCh38.p7	15:59066273	TTCAGGAAAATCCCA[A/G]TGAAGACCACTGCAT	54778
rs12913262	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59050934	AATGGGGTAAAAAAG[A/T]TTTTTCAATAAATGT	54778
rs12915899	snp	C/T	0.417359	0.185718	intron-variant	RNF111	GRCh38.p7	15:59084332	ATGCCTTGTGATTGA[C/T]TGCTTTGCAGAAGGA	54778
rs12917373	snp	A/G	0.407674	0.194008	intron-variant	RNF111	GRCh38.p7	15:59072515	ctggagtgcagtggc[A/G]tgatctcggctcact	54778
rs13379721	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59049373	TTTGAtttttttttt[A/T]tttttttttttttGG	54778
rs16940958	snp	C/T	0.0644693	0.167566	intron-variant	RNF111	GRCh38.p7	15:59017311	CAGCATATGTGACAA[C/T]GCTTATTCATAAGAG	54778
rs16940976	snp	G/T	0.0663309	0.169604	intron-variant	RNF111	GRCh38.p7	15:59023469	TTTTGTTATTCTGTA[G/T]TATTTTCTAACTAGC	54778
rs16940987	snp	A/C	0.29432	0.24604	intron-variant	RNF111	GRCh38.p7	15:59061664	TTTCCCTTCCAGTTC[A/C]TTTATCTGTGCTCTA	54778
rs16940989	snp	A/G	0.114738	0.210248	intron-variant	RNF111	GRCh38.p7	15:59070891	CCCTCAGCTTCCAGT[A/G]TTGCACAGTTGCTGT	54778
rs16940998	snp	C/G	0.430434	0.173042	intron-variant	RNF111	GRCh38.p7	15:59086095	AAGTGGTAATAGATC[C/G]GTTCTGATGCAGTCA	54778
rs16941003	snp	A/C/G	0.0134861	0.0810011	intron-variant	RNF111	GRCh38.p7	15:59088305	AGACTAGGGAGGAGA[A/C/G]GCTTTTCAGGGTAAG	54778
rs16941012	snp	C/T	0.0614824	0.164198	intron-variant	RNF111	GRCh38.p7	15:59090702	TTATAAAGATAACTT[C/T]TGCTGTACCATTTCA	54778
rs16941014	snp	A/G	0.416055	0.186885	intron-variant	RNF111	GRCh38.p7	15:59091503	TTGCCTTTCATGCCA[A/G]TTAGCTCCCACAGAT	54778
rs17190751	snp	A/C	0.162581	0.234218	intron-variant	RNF111	GRCh38.p7	15:59023436	TAAATATTTTCATTC[A/C]TCTTGTAAGTAGTAT	54778
rs17190764	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59055086	GGGTTCACAGTCACG[C/T]GTTTTAGAAGCATAA	54778
rs17236369	snp	A/G	0.493748	0.0555599	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021656	CAATTTTATAGACTA[A/G]AAACAGTTTTAGAGA	54778
rs17236383	snp	A/G	0.416871	0.186156	intron-variant	RNF111	GRCh38.p7	15:59043549	TGAGATACGACATCT[A/G]TAAGGCTAGTGAGCA	54778
rs17236411	snp	C/G	0.0322114	0.122752	intron-variant	RNF111	GRCh38.p7	15:59059962	AATTTACATCTAGCA[C/G]ATTAGAAAACTACAT	54778
rs17236432	snp	A/G	0.0279526	0.114869	intron-variant	RNF111	GRCh38.p7	15:59088012	TAGCCTTCTTGCTTT[A/G]TAAGCTTGGCTGTGA	54778
rs17236439	snp	A/C	0.0618563	0.164627	intron-variant	RNF111	GRCh38.p7	15:59089435	CTCTTTTCAAGTTTG[A/C]GCTACTAAGAGCCTC	54778
rs17236453	snp	C/T	0.416545	0.186448	intron-variant	RNF111	GRCh38.p7	15:59092156	GTCCAAGTTAAATAC[C/T]GTAACTAATGTTAAT	54778
rs17269482	snp	A/T	0.0596104	0.162024	intron-variant	RNF111	GRCh38.p7	15:59012591	ATTTGAGAAGATGAC[A/T]TGATTGGATGTTTTA	54778
rs17302142	snp	A/G	0.424193	0.179323	intron-variant	RNF111	GRCh38.p7	15:59053813	GCATTTACCTGAGTT[A/G]ATAGGCAGTGATCTT	54778
rs17302163	snp	C/T	0.489608	0.0713316	intron-variant	RNF111	GRCh38.p7	15:59076773	AGAAATGATAAATAC[C/T]CTAAGGCTATGTAAC	54778
rs17855074	snp	A/G			synonymous-codon	RNF111	GRCh38.p7	15:59031266	TAGTCTGCATTTTGG[A/G]GATTCTGATACTGTG	54778
rs28398210	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59079865	GCACAGGAATAATGA[C/G]ATGGGGTAGGGAGAG	54778
rs28399363	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59014680	CTCTCTTTGGGTGCA[C/G]AAAGAAAGCATGTTA	54778
rs28429896	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59040671	TAAGTGAACTAGTTT[C/G]AACATAAAAATTACT	54778
rs28438797	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59051807	AATAAATAAATAAAT[A/G]AATAAATAAACAAAT	54778
rs28449745	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59033069	GAGCTGTCTGAACTG[A/G]GGGAAAAGATTAATT	54778
rs28478284	snp	A/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59029865	CTTAGAATATGTGTG[A/T]ATGCTATACTTAATA	54778
rs28478417	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59093384	TGGGAGATGGTCTCC[G/T]TCTGTTGCCCAGGCT	54778
rs28493080	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:58991715	TTGATTCTAGAGAAT[C/G]TACAAATGTAAATTA	54778
rs28547529	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:58991453	CATGGAGCTGACATT[C/G]TGTTCTGTGTGTGGG	54778
rs28572002	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59081501	GTTGTTTTCTTTTTT[A/T]AAAAAAAGAACAAAG	54778
rs28733679	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59079645	AATTTGTATTGAAAT[C/T]TAAGACAAACTTTTT	54778
rs28782903	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:58998317	TAAACTTGTGTCATA[C/G]AGTTTGTTGTACAGA	54778
rs28815181	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:58998361	CAGGTATTAAGCCTA[C/G]TACCTGTTAGTTATT	54778
rs33968358	in-del	-/AGTTGGTGATTCATTCAGCAA			intron-variant	RNF111	GRCh38.p7	15:59055524	TTCTTAGGTCAATTA[-/AGTTGGTGATTCATTCAGCAA]GTTTACCGAGTGCCA	54778
rs34047420	in-del	-/T	0.449726	0.150364	intron-variant	RNF111	GRCh38.p7	15:59046184	GCTCCTATTTGCTGC[-/T]TTTTTTTTTTTTTCC	54778
rs34086812	snp	A/G	0.00302661	0.0387833	missense	RNF111	GRCh38.p7	15:59081139	TTAGCCAGTACAGCT[A/G]CACCAATCCCTCAGC	54778
rs34091016	in-del	-/AT/T/TA	0.436123	0.166908	intron-variant	RNF111	GRCh38.p7	15:59073492	CTCCAAAAAAAAAAA[-/AT/T/TA]AAATAAATAAACTAC	54778
rs34168309	in-del	-/G			intron-variant	RNF111	GRCh38.p7	15:59025169	GGATTACAGGCGTGA[-/G]CCACTGCGCCCAGGC	54778
rs34193148	snp	A/G	0.177824	0.239355	intron-variant, utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022359	AAAGTCTGTCTAAAT[A/G]TAAGGGTGGTTCCAT	54778
rs34202172	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59026724	TTTTAGAAAAAAAAA[-/A]TTTAGAACATGATAC	54778
rs34209382	in-del	-/T	0	0	intron-variant	RNF111	GRCh38.p7	15:58995788	TGCCGTGCCCCGGCC[-/T]TTTTTTTTTTTTTTT	54778
rs34278620	snp	A/G	0.209388	0.246679	intron-variant	RNF111	GRCh38.p7	15:59032191	TTATCTGCCCACCTC[A/G]GCCTCCCAAAGTGAT	54778
rs34338282	snp	C/T	0.433673	0.1696	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096897	ACGTTCCCCCAGATA[C/T]AAGTAAAGCACAGGT	54778
rs34395806	snp	A/C	0.179223	0.240105	intron-variant	RNF111	GRCh38.p7	15:59087415	GACCCTCCTCACAGT[A/C]GAAAATCAGAGTATA	54778
rs34404684	in-del	-/AC/CA	0	0	intron-variant	RNF111	GRCh38.p7	15:59077117	GAAAACATTTAGCAA[-/AC/CA]GTTTTTACAAAGCAT	54778
rs34407560	snp	C/T	0.419936	0.183362	intron-variant	RNF111	GRCh38.p7	15:59073397	GAGGTAAGATAATTG[C/T]CTGAACCTGGGAGGT	54778
rs34432774	in-del	-/T/TT	0.494692	0.0512434	upstream-variant-2KB	RNF111	GRCh38.p7	15:58986516	CCACCGCGCCCAGCC[-/T/TT]TTTTTTTTTTTTTTC	54778
rs34443683	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59025171	ATTACAGGCGTGAGC[C/G]ACTGCGCCCAGGCAG	54778
rs34509207	in-del	-/C			intron-variant	RNF111	GRCh38.p7	15:59045752	TAACAAGTAACATGT[-/C]CTGCAAAGTCAATGG	54778
rs34527160	in-del	-/A	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59073482	TGAGACACCATCTCC[-/A]AAAAAAAAAAAAATA	54778
rs34531720	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59001431	TTTTTGTTGTTGATT[-/A]AAAAAAAAATTCTTT	54778
rs34594493	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59040120	TTGAATTTAACCTAA[-/T]TTTTTTTTTTTAAAG	54778
rs34663890	in-del	-/C			intron-variant	RNF111	GRCh38.p7	15:59042648	TTTTTTTTCATGTGA[-/C]CTATACAGTTGTCCC	54778
rs34706876	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59022960	TCTTTGAAAGTGAGG[-/A]AATTGGCTGGGCGCG	54778
rs34718679	snp	C/T	0.433963	0.169285	intron-variant	RNF111	GRCh38.p7	15:59017947	TATTTTTGGTAGAGA[C/T]GGGGTTTCATCATGT	54778
rs34725448	in-del	-/T/TT	0.206642	0.246211	intron-variant	RNF111	GRCh38.p7	15:59028781	AATTTTTTTTTTTTT[-/T/TT]CTTGAGATAGAGTCT	54778
rs34738650	snp	C/T	0.0607341	0.163335	intron-variant	RNF111	GRCh38.p7	15:59002740	CTACCTGATCTGGCC[C/T]TGACTACTTCTGATG	54778
rs34815486	in-del	-/G			intron-variant	RNF111	GRCh38.p7	15:59086925	AATAGATGTAAATGT[-/G]GGGAAACCAGTTAGG	54778
rs34844437	in-del	-/C	0.492679	0.0600586	intron-variant	RNF111	GRCh38.p7	15:59083875	ATAATGTTAAAATTA[-/C]CTTTTTCCTTGGGTG	54778
rs34859729	snp	C/G	0.410737	0.191478	intron-variant	RNF111	GRCh38.p7	15:59070117	TGGGCTTAAGTAATC[C/G]TCCTGCCCCAGACTT	54778
rs34868598	snp	G/T	0.181978	0.240568	downstream-variant-500B	RNF111	GRCh38.p7	15:59097569	ATTTGAACCATAACA[G/T]TTGACTTAGAGAAAA	54778
rs34877400	snp	C/G	0.137527	0.223271	intron-variant	RNF111	GRCh38.p7	15:59000733	AAAAAAAGATAACTG[C/G]TGCTGCAGAGAATTA	54778
rs34884391	snp	G/T	0.441432	0.160792	intron-variant	RNF111	GRCh38.p7	15:59073583	AATCACATCTTCAGG[G/T]TCCAACTTCTTATTC	54778
rs34914229	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59046091	TTCCAGAATATAAAT[A/C]CAATATTATTAAGTA	54778
rs34937440	snp	G/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59087954	ATGGGGCACCTCTTA[G/T]ATTACGTACGGTAAG	54778
rs34965573	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59018382	ATTTTATGCCTAGCC[-/A]AAGATTCCTGTAAAA	54778
rs34968014	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:58994500	TTTTTTTTTTTGAGG[G/T]GGAGTCTCGCTGTGT	54778
rs34968152	in-del	-/G			intron-variant	RNF111	GRCh38.p7	15:58994503	TTTTTTTGAGGTGGA[-/G]GTCTCGCTGTGTTGC	54778
rs34974222	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59026768	AGCGATGGATTTTAG[-/A]AAAAAAAATAGTATG	54778
rs35013771	snp	A/T	0.430583	0.172886	intron-variant	RNF111	GRCh38.p7	15:59071702	TCGCAAAAAAAAAAA[A/T]AAATAAAGTTTTTGG	54778
rs35056899	in-del	-/A	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59000724	GCTGAACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	54778
rs35066133	snp	C/G	0.492287	0.0616198	intron-variant	RNF111	GRCh38.p7	15:59081917	GTGGTCCCAGCTACT[C/G]GGTAGGCTGAGATGA	54778
rs35067970	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59007413	ATCAGTAGTTCCTTC[-/T]TTTGTTGTTGCTGTT	54778
rs35154303	in-del	-/T	0.495368	0.0478996	intron-variant	RNF111	GRCh38.p7	15:59019122	TTTTGTATTTTTGTA[-/T]TTTTTTTTTTTTTTT	54778
rs35155563	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59023535	AGTGTTATTTTTATT[-/T]ATATATTTTTGGTAA	54778
rs35210199	snp	A/G	0.421368	0.182025	intron-variant	RNF111	GRCh38.p7	15:59017888	TCAGCCTCCCGAGTA[A/G]CTGGGATTACAGGCG	54778
rs35304473	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59088298	GGAAAGAGACTAGGG[-/T]AGGAGAGGCTTTTCA	54778
rs35375652	in-del	-/T/TT	0.480697	0.0963277	intron-variant	RNF111	GRCh38.p7	15:58995465	TTGTTTTTTTTTTTT[-/T/TT]GACGGAGTCTCACTC	54778
rs35410395	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59072880	TGCAATTTTTTTATT[-/A]AAAAAAAAAAAAACA	54778
rs35441339	in-del	-/AT			intron-variant	RNF111	GRCh38.p7	15:59023540	TATTTTTATTTATAT[-/AT]TTTTGGTAAATATAT	54778
rs35446247	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:58989570	TGGTGTCTGTTGGCC[-/A]CTTGTTTGCTAGTTA	54778
rs35460138	snp	C/T	0.4444	0.15719	intron-variant	RNF111	GRCh38.p7	15:59093200	TGGCCAGGGAAATTT[C/T]GTAGTCAAAATTGTC	54778
rs35486378	in-del	-/C			intron-variant	RNF111	GRCh38.p7	15:59077634	ATACCCCCATAATAT[-/C]CCATTGTATATTAAA	54778
rs35498817	in-del	-/AGA	0.475965	0.106957	upstream-variant-2KB	RNF111	GRCh38.p7	15:58986700	TTGTATTTTTAGTGG[-/AGA]AGGAGTTTCACCATG	54778
rs35523890	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59024676	CTTTTGAATTATTTT[-/T]GGTCGTTTAAATGTA	54778
rs35527453	snp	A/G	0.467439	0.123371	intron-variant	RNF111	GRCh38.p7	15:59070269	CTTGATTGTCCTTCG[A/G]GAATAAGAATTGAAT	54778
rs35555888	snp	A/G	0.442926	0.158996	intron-variant	RNF111	GRCh38.p7	15:59093935	TGGGATACTTTTTAA[A/G]GCTATTATTTTAACA	54778
rs35563547	in-del	-/A/AA	0.477684	0.103247	intron-variant	RNF111	GRCh38.p7	15:59083143	GCTTAAAAAAAAAAA[-/A/AA]GAAGCAAAAAATGAA	54778
rs35612781	snp	A/C/G	1.64743e-05	0.00287	missense	RNF111	GRCh38.p7	15:59058419	CTAGCGCTTCCATTA[A/C/G]CAATTCAAATCCATC	54778
rs35658945	snp	A/C	0.420096	0.183214	intron-variant	RNF111	GRCh38.p7	15:59018053	TATGAGGCACCACGC[A/C]CGGCCTATTTGTTGA	54778
rs35669929	in-del	-/GT			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986195	ATTTTAAAATCATTT[-/GT]GTGTGTGTGTGTGTG	54778
rs35673657	in-del	-/T	0.307423	0.243316	intron-variant	RNF111	GRCh38.p7	15:58989875	TTAGATGTTTCCTTC[-/T]TTTTTTTTTTGTTAT	54778
rs35689684	in-del	-/A	0.413914	0.188765	intron-variant	RNF111	GRCh38.p7	15:59002556	ACTGTGCATTTAATT[-/A]AAAAAAAAAAAAGAG	54778
rs35703721	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59050470	TGTAAATTATACCTC[-/A]AAAAAACTATTTTAA	54778
rs35724526	in-del	-/CTT	0.427879	0.175668	intron-variant	RNF111	GRCh38.p7	15:59054638	ATTAACTTTATACTC[-/CTT]CTTAAGAATTTTATT	54778
rs35734562	in-del	-/G			intron-variant	RNF111	GRCh38.p7	15:59005941	AGTCACAGCAGTGAT[-/G]GGGGATGTGGAGATT	54778
rs35769647	snp	A/T	0.40595	0.195396	intron-variant	RNF111	GRCh38.p7	15:59081670	CAAAGCTGAGCTATG[A/T]CTGTGCCACTGCACT	54778
rs35787227	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:58994495	CTTATTTTCTCTCTC[-/T]TTTTTTTTTTTTTTT	54778
rs35804813	in-del	-/AA			intron-variant	RNF111	GRCh38.p7	15:59064536	GCAAGACTTTGTCGC[-/AA]AAAAAAAAAAAAAAA	54778
rs35858450	in-del	-/C/CTC/TC/TTC	0.358486	0.242559	intron-variant	RNF111	GRCh38.p7	15:59093361	TTTTTTTTTTTTTTT[-/C/CTC/TC/TTC]CCTTTTCTGGGAGAT	54778
rs35955825	in-del	-/G			intron-variant	RNF111	GRCh38.p7	15:59024786	TCCACAACTTTTTAT[-/G]CTTCCCCGACTGAAA	54778
rs35956973	in-del	-/G			intron-variant	RNF111	GRCh38.p7	15:58990098	AGGGCTAAGGACAGG[-/G]AGATCTAGATTTTAG	54778
rs35962781	in-del	-/C			frameshift-variant	RNF111	GRCh38.p7	15:59058472	CTGCTTCAGCTGTCA[-/C]CCAGTAGCCAACCTT	54778
rs35989790	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59072451	GCTGTCATTTCCATC[-/T]TTTTTTTTTTTTTTT	54778
rs36006109	in-del	-/TA	0.0244538	0.107838	intron-variant	RNF111	GRCh38.p7	15:59016162	ATGTATATATATATA[-/TA]GTTTTTTTTTTTTAG	54778
rs36023222	in-del	-/G			intron-variant	RNF111	GRCh38.p7	15:59002460	CATGGTAAATACGGG[-/G]AAGTACGGTTGAGTA	54778
rs36033677	in-del	-/G			intron-variant	RNF111	GRCh38.p7	15:59001150	GGGAAGAGCATTCAA[-/G]GGCAGCGTGACTAGC	54778
rs36057944	in-del	-/T	0.469148	0.120308	intron-variant	RNF111	GRCh38.p7	15:59079656	AAATCTAAGACAAAC[-/T]TTTTTTTTTTTTTTA	54778
rs36101247	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59012947	TTCGCCATGTTGGCC[-/A]AGGCTGGTCTTGAAC	54778
rs36104087	in-del	-/G			intron-variant	RNF111	GRCh38.p7	15:59094400	TGAGATAATATGTAT[-/G]TTTTAAAGGGCATTA	54778
rs36106236	in-del	-/C			intron-variant	RNF111	GRCh38.p7	15:59073597	TTCCAACTTCTTATT[-/C]CTAGTTCTCTTGCTG	54778
rs36116249	in-del	-/C	0.415563	0.18732	intron-variant	RNF111	GRCh38.p7	15:59074793	GTGCAAGAGGCCTAG[-/C]TTTTGGCCTCTCTGG	54778
rs36125140	snp	C/G	0.43555	0.167544	intron-variant	RNF111	GRCh38.p7	15:59071554	AAAAATTAGCTGGGC[C/G]TGGGGTCTCGTGCCT	54778
rs55646764	snp	G/T	0.0260105	0.111035	intron-variant	RNF111	GRCh38.p7	15:58991831	TACAATATGTTGGTG[G/T]TGTTTAAACCCTGAC	54778
rs55671218	snp	C/T	0.489722	0.0709447	utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58987920	CGGTGACAGACACTG[C/T]TCTTGACTCTAGGGG	54778
rs55837057	snp	A/G	0.0174175	0.0916809	intron-variant	RNF111	GRCh38.p7	15:59002353	ATAGCTGTCCCTTCC[A/G]TTTTCCCATGGTATT	54778
rs55905765	snp	A/T	0.0217236	0.101931	intron-variant, utr-variant-5-prime	RNF111	GRCh38.p7	15:58988231	GACTTAGGGTCTGGG[A/T]CTCCGCAGACGATTT	54778
rs56152718	snp	C/T	0.0130921	0.0798413	intron-variant	RNF111	GRCh38.p7	15:59050557	ATGGACCGTAAAATA[C/T]GTGTAATATTTAAGA	54778
rs56172115	in-del	-/T/TT	0.625	0.125	intron-variant	RNF111	GRCh38.p7	15:59028794	AATTTTTTTTTTTTT[-/T/TT]CTTGAGATAGAGTCT	54778
rs56260073	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59007179	TCCTTATGAAGGTAT[-/T]GAACACGAACAACCA	54778
rs56304637	snp	G/T	0.138207	0.223612	intron-variant	RNF111	GRCh38.p7	15:59034026	AAATAAAAGTTTATC[G/T]CTTCTTCAGATCCTC	54778
rs56334435	snp	C/T	0.416545	0.186448	intron-variant	RNF111	GRCh38.p7	15:59073064	GTGGTCCTAGCTACT[C/T]GGGAGGCTGAAGTTG	54778
rs56353210	snp	C/G	0.0256215	0.110247	intron-variant	RNF111	GRCh38.p7	15:58992917	ACACCTGTAGTAATC[C/G]TAGCACTTTGGGAGG	54778
rs56358103	in-del	-/AAATAAATAAATAAAT			intron-variant	RNF111	GRCh38.p7	15:59051791	AATAAATAAATAAAT[-/AAATAAATAAATAAAT]GAATAAATAAACAAA	54778
rs56366071	snp	G/T	0.0310518	0.120672	intron-variant	RNF111	GRCh38.p7	15:59025488	GTAGTAGTAGTTATA[G/T]GTAGTAGAAGAGAAT	54778
rs56679928	snp	C/T	0.0158469	0.0875917	intron-variant	RNF111	GRCh38.p7	15:59067452	ACCTTTCTTTTTTAA[C/T]TGTGGTGGCTTTGGG	54778
rs56879271	snp	C/G	0.0162398	0.0886349	intron-variant	RNF111	GRCh38.p7	15:59093949	AGGCTATTATTTTAA[C/G]AAGATATTAGGAAGT	54778
rs56959347	in-del	-/AA	0	0	intron-variant	RNF111	GRCh38.p7	15:59078574	AAAAAAAAAAAAAAA[-/AA]GACCAGGCACAGTGG	54778
rs57057009	snp	C/T	0.0558544	0.157504	intron-variant	RNF111	GRCh38.p7	15:59000644	GAACTGGGAGGCAGA[C/T]GTTTCAGTGAGCCAA	54778
rs57093568	snp	C/G	0.00953873	0.0683987	intron-variant	RNF111	GRCh38.p7	15:59032953	ATAAGTTTATTTGCA[C/G]ACAGTCCTGAAATGT	54778
rs57283614	in-del	-/AA	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59064553	AAAAAAAAAAAAAAA[-/AA]GGAAATAATTTGTCG	54778
rs57291032	in-del	-/GTGTGT			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986201	TGTGTGTGTGTGTGT[-/GTGTGT]TTTGTTTGTTTGTTT	54778
rs57361749	snp	A/T	0.416382	0.186593	intron-variant	RNF111	GRCh38.p7	15:59091352	AGTCCTTCTTCCCAG[A/T]AGTGAAATCATAGTT	54778
rs57452205	snp	A/G	0.0517044	0.152246	intron-variant	RNF111	GRCh38.p7	15:58992985	ACCAGCCTGCCCAAC[A/G]TGGCAAAACCCTGTC	54778
rs57557135	snp	C/G	0.419936	0.183362	intron-variant	RNF111	GRCh38.p7	15:59054018	TTGGCTCACCGCAGC[C/G]TCCATCTCCTGGGTT	54778
rs57603440	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59053881	CTCTTATTGTTATTA[A/T]GAGATATTAATTTTG	54778
rs57629829	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59044123	GCAACCCCCACCTCC[C/G/T]GGGTTCAAGCGATTC	54778
rs57750394	snp	C/T	0.0460142	0.144533	intron-variant	RNF111	GRCh38.p7	15:59013018	TGCTGAGATTATAGG[C/T]GTGAGCCACCGCGAC	54778
rs57803886	snp	C/T	0.0663309	0.169604	intron-variant	RNF111	GRCh38.p7	15:59068286	TGTAATTTTGACATA[C/T]ACTATTCCAGAAAAA	54778
rs57915821	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59072893	TTAAAAAAAAAAAAA[-/A]CAAAACACTTCCAGC	54778
rs58003688	snp	C/T	0.0217236	0.101931	intron-variant	RNF111	GRCh38.p7	15:58999150	TGTGAAACTGGATTT[C/T]CTTATAATTTAACCA	54778
rs58087223	snp	A/G	0.412917	0.189626	intron-variant	RNF111	GRCh38.p7	15:59075132	AATAATGAGAAAAAT[A/G]TAAATATTAAGAGAA	54778
rs58335303	snp	C/G	0.466204	0.125522	intron-variant	RNF111	GRCh38.p7	15:59073206	CTGGGTGCAGTGGCT[C/G]ACTTCTGTAATCCCA	54778
rs58417366	snp	A/G	0.495135	0.0490805	intron-variant	RNF111	GRCh38.p7	15:59054022	CTCACCGCAGCCTCC[A/G]TCTCCTGGGTTCAAG	54778
rs58594305	in-del	-/A	0.413083	0.189483	intron-variant	RNF111	GRCh38.p7	15:59078867	CCCTCTCAAAAGAAG[-/A]AAAAAAAAAAAAAAA	54778
rs58677882	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59053880	TCTCTTATTGTTATT[A/C]AGAGATATTAATTTT	54778
rs58684833	snp	G/T	0.0256215	0.110247	intron-variant	RNF111	GRCh38.p7	15:59026532	GCCTCCTTTGTAAAT[G/T]AGATCAGCCAATAAT	54778
rs58827061	snp	A/C	0.0670745	0.170406	intron-variant	RNF111	GRCh38.p7	15:59062735	TGAAGTAACATATCC[A/C]AGGTTATATGATAGT	54778
rs59050314	snp	C/G	0.0126979	0.078662	intron-variant	RNF111	GRCh38.p7	15:59027731	CAGGGTTTCTTTTCA[C/G]CATGTTGGTCAGGCT	54778
rs59125511	snp	C/T	0.0984431	0.198823	intron-variant	RNF111	GRCh38.p7	15:59013707	GTTTCAACTCCTGAA[C/T]GAGGGAGTGTCCACA	54778
rs59282449	snp	A/G	0.405255	0.195948	intron-variant	RNF111	GRCh38.p7	15:59078881	GAAAAAAAAAAAAAA[A/G]AGAGAGGTATAGGTA	54778
rs59440204	snp	G/T			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021161	GCCCTGCCTTTTTTT[G/T]TTTGTTTGAGATGAA	54778
rs59514650	snp	A/G	0.405255	0.195948	intron-variant	RNF111	GRCh38.p7	15:59078625	CACTTTCGGGAGGCC[A/G]AGGCGGGTGGATCAC	54778
rs59522599	snp	A/T	0.0209421	0.100162	upstream-variant-2KB	RNF111	GRCh38.p7	15:58987159	GACGCATTTGTTATC[A/T]ACTGACTTTTATAAA	54778
rs59540276	snp	A/G	0.433236	0.170072	intron-variant	RNF111	GRCh38.p7	15:59037559	TTAATAGGTATTGCC[A/G]GGCGTGGTGGCTCAC	54778
rs60026626	snp	G/T			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021162	CCCTGCCTTTTTTTG[G/T]TTGTTTGAGATGAAG	54778
rs60072785	snp	C/T	0.159292	0.232964	intron-variant	RNF111	GRCh38.p7	15:59064251	CTAAAAAGTAAATAA[C/T]CTGGCCGGGCGTGGT	54778
rs60123130	in-del	-/T/TA	0.625	0.125	intron-variant	RNF111	GRCh38.p7	15:59073493	TCCAAAAAAAAAAAA[-/T/TA]AATAAATAAACTACT	54778
rs60262196	snp	C/G	0.404035	0.196909	intron-variant	RNF111	GRCh38.p7	15:59088853	AATGAAACTTATTCT[C/G]TCCATAAGGTGTATG	54778
rs60285686	snp	G/T	0.409891	0.192184	intron-variant	RNF111	GRCh38.p7	15:59079829	GATGGGAAACAAATA[G/T]GTCTCCTTCACCTTA	54778
rs60350601	in-del	-/TTTTTTTTTT	0	0	intron-variant	RNF111	GRCh38.p7	15:58996669	TTTTTTTTTTTTTTT[-/TTTTTTTTTT]ACCCAGGCAGTTACT	54778
rs60501070	in-del	-/TT			intron-variant	RNF111	GRCh38.p7	15:59033407	CACAAATACTTTTTT[-/TT]GAGAAGAGTTCATTT	54778
rs60533405	snp	C/T	0.0629771	0.165899	intron-variant	RNF111	GRCh38.p7	15:59002748	TCTGGCCCTGACTAC[C/T]TCTGATGTCATTGTG	54778
rs60624328	snp	A/G	0.0383715	0.133092	intron-variant	RNF111	GRCh38.p7	15:59070061	TTTTTTTTTTTTTTA[A/G]AGAGGATCTTGCCTT	54778
rs60628647	snp	A/G	0.067446	0.170804	intron-variant	RNF111	GRCh38.p7	15:59062920	GCATCCTTGGTTTGT[A/G]GCCTCTAAATTCCAG	54778
rs60668889	in-del	-/T	0.0228947	0.104514	intron-variant	RNF111	GRCh38.p7	15:59024519	AGGAAGAGAGGGTGA[-/T]TTTTTTAAAGTGTGT	54778
rs60727965	in-del	-/T/TT	0	0	intron-variant	RNF111	GRCh38.p7	15:59049765	TTTTTTTTTTTTTTT[-/T/TT]GAGATGGGGTCTCGC	54778
rs60741546	snp	C/T	0.409891	0.192184	intron-variant	RNF111	GRCh38.p7	15:59079831	TGGGAAACAAATAGG[C/T]CTCCTTCACCTTAAT	54778
rs60882297	snp	C/T	0.0883596	0.190715	intron-variant	RNF111	GRCh38.p7	15:58990886	TTGAATGTCTTATAC[C/T]TCTGTTTGTTTCTTT	54778
rs60899149	snp	G/T	0.0517044	0.152246	intron-variant	RNF111	GRCh38.p7	15:58993338	ACATGGTGAAACCTT[G/T]TCTCTACTAAAAACA	54778
rs60929391	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59067254	TCCTTTTTTTTTTTT[-/T]AACTCCCTCCCATTC	54778
rs60964484	snp	A/G	0.0341408	0.126114	intron-variant	RNF111	GRCh38.p7	15:59006979	TTTTAGTAGAAATGG[A/G]GTTTCACCATCTTGG	54778
rs61022867	snp	A/G	0.416545	0.186448	intron-variant	RNF111	GRCh38.p7	15:59043385	TGGTCTTGAACTCCT[A/G]ACCTCAGGTGATCTG	54778
rs61149070	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59018440	TGTGTAGAAATCTGT[G/T]GTCAACAAAGTTGTG	54778
rs61157686	snp	A/T	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:59056934	AGTAAGTTCAACCAG[A/T]ATTTACACTTTACTG	54778
rs61292111	in-del	-/T/TC	0	0	upstream-variant-2KB	RNF111	GRCh38.p7	15:58986530	CTTTTTTTTTTTTTT[-/T/TC]CTTGGAGACGGAGTC	54778
rs61595263	in-del	-/GGTGATTCATTCAGCAAAGTT	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59055527	TTAGGTCAATTAGTT[-/GGTGATTCATTCAGCAAAGTT]TACCGAGTGCCAGTC	54778
rs61690344	snp	A/G	0.0611083	0.163768	intron-variant	RNF111	GRCh38.p7	15:59017092	TTGCAATGCAATGAT[A/G]ATAGAAACAAAGTGC	54778
rs61690767	snp	C/T	0.146314	0.227484	intron-variant	RNF111	GRCh38.p7	15:59083073	AGGATCACTTAAGCC[C/T]GGGAGTTCAGGGTTA	54778
rs62002480	snp	C/T			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986180	TTGTAATTTTAAAAT[C/T]ATTTGTGTGTGTGTG	54778
rs62002481	snp	G/T			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986185	ATTTTAAAATCATTT[G/T]TGTGTGTGTGTGTGT	54778
rs62002482	snp	A/G	0.0283406	0.115616	upstream-variant-2KB	RNF111	GRCh38.p7	15:58987242	GACCACTTTTGATCT[A/G]ATTCCGGAAGCAAAT	54778
rs62002511	snp	A/C	0.151334	0.229706	intron-variant	RNF111	GRCh38.p7	15:58994359	CATTTTTATTTTGAC[A/C]TAATTTCAAACTTAC	54778
rs62002512	snp	C/T	0.0170251	0.090679	intron-variant	RNF111	GRCh38.p7	15:58998152	TCGTGATCCGCCAGC[C/T]TCGGCCTCCCAAAGT	54778
rs62002513	snp	A/G	0.0729998	0.176553	intron-variant	RNF111	GRCh38.p7	15:59000763	AACCAATTTTTGATG[A/G]TAGATGAGCCCACTA	54778
rs62002515	snp	C/T	0.14933	0.228835	intron-variant	RNF111	GRCh38.p7	15:59004639	AACAAGAATTTTCAC[C/T]TCACTGTCTGAATAT	54778
rs62002516	snp	C/T	0.490007	0.0699769	intron-variant	RNF111	GRCh38.p7	15:59009703	CTCATGCCTGTAATC[C/T]CAACACTTTGAGAAG	54778
rs62002519	snp	A/T			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021868	TTTCTAGCTTCTTAT[A/T]AATTTTTTTTTGAGT	54778
rs62002521	snp	A/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59036999	CAACTACAGTTGACT[A/T]ATTTTTTTTTTTTTT	54778
rs62002543	snp	A/C	0.406641	0.194842	intron-variant	RNF111	GRCh38.p7	15:59066646	TATCACATTATTTAC[A/C]GAGATTTGAAATTAC	54778
rs62002544	snp	A/G	0.410905	0.191336	intron-variant	RNF111	GRCh38.p7	15:59066663	AGATTTGAAATTACC[A/G]AACATTTCTTTAAAC	54778
rs62002554	snp	C/G	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59080467	TTATGGCAACCTTTT[C/G]GAAAGGGTATTTTTA	54778
rs62002557	snp	G/T	0.145978	0.227331	intron-variant	RNF111	GRCh38.p7	15:59082126	TCCTCATTTCACTAA[G/T]AAATTGATTCTTTGC	54778
rs62004074	snp	A/G	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59090743	GAAAACATGATAAAC[A/G]ACCATTTGCCTTACT	54778
rs66469077	in-del	-/TG	0.250732	0.249999	upstream-variant-2KB	RNF111	GRCh38.p7	15:58986184	AATTTTAAAATCATT[-/TG]TGTGTGTGTGTGTGT	54778
rs66813949	in-del	-/AATAAATAAATAAATA	0.454544	0.143743	intron-variant	RNF111	GRCh38.p7	15:59051772	GTGAGAAACTGTCTC[-/AATAAATAAATAAATA]AATAAATAAATAAAT	54778
rs66850661	in-del	-/TTCTTGTCAGGCTG			intron-variant	RNF111	GRCh38.p7	15:59019558	GGGTTTATACACCAT[-/TTCTTGTCAGGCTG]TCTTGTCAGGCTTAA	54778
rs68017695	in-del	-/AAG	0.5	0	upstream-variant-2KB	RNF111	GRCh38.p7	15:58986702	GTATTTTTAGTGGAG[-/AAG]GAGTTTCACCATGTT	54778
rs71119423	in-del	-/AC	0	0	upstream-variant-2KB	RNF111	GRCh38.p7	15:58986205	AAACAAACAAACAAA[-/AC]ACACACACACACACA	54778
rs71119428	in-del	-/A	0	0	intron-variant	RNF111	GRCh38.p7	15:59012744	GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAGA	54778
rs71119429	in-del	-/AA/G	0	0	intron-variant	RNF111	GRCh38.p7	15:59062070	GACCCTGTCTCGGGG[-/AA/G]AAAAAAAAAAAAAAA	54778
rs71425831	in-del	-/C	0.5	0	intron-variant	RNF111	GRCh38.p7	15:58992304	CCGTCTCGGCCTCCC[-/C]AAAGTGCTGGGATTA	54778
rs71425833	in-del	-/G	0.5	0	intron-variant	RNF111	GRCh38.p7	15:58996445	AGTAGCCAAGTGGGG[-/G]TGGTGCATGCCTGTA	54778
rs71425834	in-del	G/TT	0.5	0	intron-variant	RNF111	GRCh38.p7	15:58996556	ACTGTACTCCAGCCT[G/TT]GGCAGTAGAGCAAGA	54778
rs71425835	in-del	-/TTTT	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59000178	CTTTTTTTTTTTTTT[-/TTTT]GAGACAGGGTCTCTC	54778
rs71425836	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59012032	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCGC	54778
rs71425837	in-del	-/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59053878	TATCTCTTATTGTTA[-/T]TAAGAGATATTAATT	54778
rs71425838	snp	A/C	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59068225	ATGCTGTCTCAAAAA[A/C]CAACAACAACAACAA	54778
rs71478699	snp	A/G	0.152667	0.230274	intron-variant	RNF111	GRCh38.p7	15:59005129	CCTATACTGTCAGCC[A/G]TTAAAGTGTCAGTAA	54778
rs71478700	snp	C/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59018446	GAAATCTGTTGTCAA[C/T]AAAGTTGTGTTCTAA	54778
rs71478701	snp	G/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59023579	TGGCCTGTCTTACTG[G/T]TGCCAGTGGTTTTCT	54778
rs71478702	snp	A/G	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59090817	AATCTCAGCAGTTTA[A/G]GAGGCCGAGGTGGGA	54778
rs72098856	in-del	-/AA	0.495135	0.0490805	intron-variant	RNF111	GRCh38.p7	15:59053880	TCTCTTATTGTTATT[-/AA]GAGATATTAATTTTG	54778
rs72495075	in-del	-/TTGG			intron-variant	RNF111	GRCh38.p7	15:59049385	TTTTTTTTTTTTTTT[-/TTGG]CCACCTAGTATGCCA	54778
rs72525815	in-del	-/AC	0.44768	0.153045	intron-variant	RNF111	GRCh38.p7	15:59077116	GGAAAACATTTAGCA[-/AC]AGTTTTTACAAAGCA	54778
rs72745097	snp	A/C	0.386694	0.20932	upstream-variant-2KB	RNF111	GRCh38.p7	15:58987116	ACTCTGAAGCTCATC[A/C]TCTCTCTATCCTCCT	54778
rs72746807	snp	G/T	0.117985	0.21263	intron-variant	RNF111	GRCh38.p7	15:59018963	GCGCCATGCTCTGTC[G/T]CCCAGGTTGGAGTGC	54778
rs72746811	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59044782	CTTTTAAGTCGTGCT[A/G]TTTAATAAGATTAAC	54778
rs72746812	snp	G/T	0.0287284	0.116357	intron-variant	RNF111	GRCh38.p7	15:59068612	CTCCGAAGTTCGTTT[G/T]TTTTTCTTTTTTTTG	54778
rs73414877	snp	C/T	0.00835141	0.0640778	upstream-variant-2KB	RNF111	GRCh38.p7	15:58987126	TCATCCTCTCTCTAT[C/T]CTCCTAATGCATATA	54778
rs73414883	snp	C/G	0.137187	0.223099	intron-variant	RNF111	GRCh38.p7	15:58990142	TGCTATACATTAGAT[C/G]TCCGAGTTTATTGTT	54778
rs73414887	snp	A/T	0.253264	0.249979	intron-variant	RNF111	GRCh38.p7	15:58991703	ATTAGGTGAGGTTTG[A/T]TTCTAGAGAATCTAC	54778
rs73414896	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59001242	GTGAGGAGGAGAATG[A/G]TGGTCTCTGAGAACA	54778
rs73414897	snp	A/G	0.0130921	0.0798413	intron-variant	RNF111	GRCh38.p7	15:59001627	AGGTTCACTTTAGGA[A/G]GACTAAGTCTATTTT	54778
rs73416803	snp	A/G	0.0126979	0.078662	intron-variant	RNF111	GRCh38.p7	15:59005212	GTTTGTTTATTTGTC[A/G]AGACAGTCTCACCTA	54778
rs73416807	snp	C/T	0.0130921	0.0798413	intron-variant	RNF111	GRCh38.p7	15:59005251	AGGCTGATCTCAAAC[C/T]CCTGGGCACAAGCAG	54778
rs73416826	snp	A/G	0.0134861	0.0810011	intron-variant	RNF111	GRCh38.p7	15:59015745	CCCTGTGCATCCTTC[A/G]TGGTTTGACTTGGAT	54778
rs73416846	snp	C/T	0.0130921	0.0798413	intron-variant	RNF111	GRCh38.p7	15:59027061	TTTAGTTAATTGTGC[C/T]GTGAATTGCTTCTTT	54778
rs73416900	snp	A/G	0.0988009	0.199095	intron-variant	RNF111	GRCh38.p7	15:59067990	GTTCGCAAAATGTCA[A/G]CTAGTATTAAATTAG	54778
rs73418820	snp	A/G	0.0162398	0.0886349	intron-variant	RNF111	GRCh38.p7	15:59079916	TGTTTACACCCTATT[A/G]TGACAGAGCTTCCAT	54778
rs73418826	snp	A/G	0.197703	0.244469	intron-variant	RNF111	GRCh38.p7	15:59081616	AATCCCCAGTTGCTC[A/G]GGAGGCTAAGGCAGG	54778
rs73418837	snp	C/G	0.00636936	0.0560724	intron-variant	RNF111	GRCh38.p7	15:59083115	GATTGTGCCACTGCA[C/G]TTGATCCTGGAGCAA	54778
rs74017335	snp	C/T	0.0107246	0.0724382	intron-variant	RNF111	GRCh38.p7	15:58989177	GATAGTTTATTACTA[C/T]ATGTATTTTTGTAAA	54778
rs74017337	snp	A/G	0.0225045	0.103662	intron-variant	RNF111	GRCh38.p7	15:59007825	TAAAATCTTTTGCCT[A/G]TTTTTTGTGGGGTTG	54778
rs74017338	snp	A/C	0.0225045	0.103662	intron-variant	RNF111	GRCh38.p7	15:59009485	TCAAAGTTTTCTGAT[A/C]TGAAATTATCAAATT	54778
rs74017339	snp	G/T	0.0599851	0.162463	intron-variant	RNF111	GRCh38.p7	15:59009535	AATTTGATAATTTCA[G/T]ATCAGAAAACTTTGA	54778
rs74017340	snp	A/G	0.138886	0.22395	intron-variant	RNF111	GRCh38.p7	15:59013313	ACGTTTGTCATGACT[A/G]AGAGACCCACATTGA	54778
rs74017345	snp	A/G	0.0629771	0.165899	intron-variant	RNF111	GRCh38.p7	15:59057787	TCTCTGTAAGGCATC[A/G]TACGAAGTATGTGAT	54778
rs74017350	snp	A/G	0.0225045	0.103662	intron-variant	RNF111	GRCh38.p7	15:59077002	AAAAAAATCTGCATC[A/G]TGCAGACGCAGCTGG	54778
rs74017351	snp	A/T	0.0221141	0.102801	intron-variant	RNF111	GRCh38.p7	15:59084509	AAAAATAATAATTGT[A/T]TATATTTGGAGGTAC	54778
rs74017352	snp	A/T	0.0174175	0.0916809	intron-variant	RNF111	GRCh38.p7	15:59088913	AGCACTTCAGCTCTA[A/T]GCTTGGGTGCCATTT	54778
rs74017353	snp	C/T	0.0341062	0.126055	intron-variant	RNF111	GRCh38.p7	15:59093361	TTTTTTTTTTTTTTT[C/T]CCTTTTCTGGGAGAT	54778
rs74017355	snp	A/T	0.00279162	0.0372561	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096442	TTGTCTTTGTGTTTC[A/T]TAATTAGTTTTTATA	54778
rs74017356	snp	A/G	0.0678174	0.1712	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096546	CATTTATATTCATTC[A/G]GTTATGACTACTTGC	54778
rs74017357	snp	A/G	0.067446	0.170804	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096796	TGTAATGGATGTACT[A/G]CTTTGCCACTGGAAT	54778
rs74360936	snp	C/T	0.0569829	0.158885	intron-variant	RNF111	GRCh38.p7	15:59006557	GAATTGTACAGTGAA[C/T]GCCCATCTCCCTGCC	54778
rs74400119	snp	A/T	0.0279526	0.114869	intron-variant	RNF111	GRCh38.p7	15:59069712	ACAGTTTGAGACTCA[A/T]GTTGATGTTTGTAGG	54778
rs74431474	snp	C/T	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59030005	TGATATTTACTATTA[C/T]ATTATTTTCATATGT	54778
rs74433142	snp	A/G	0.0126979	0.078662	intron-variant	RNF111	GRCh38.p7	15:59009373	TATCTCTGTGAGGGA[A/G]GATGCTAGTAGAACC	54778
rs74478572	snp	A/G	0.00755907	0.0610114	intron-variant	RNF111	GRCh38.p7	15:59030649	CGTTTTATAAGAATA[A/G]TAAAATAATTCATAA	54778
rs74480339	snp	A/T	0.0696718	0.173152	intron-variant	RNF111	GRCh38.p7	15:59092135	AGTACATTCAAGTTT[A/T]CAACTGTCCAAGTTA	54778
rs74540610	snp	G/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59017771	TTTTTTTTTTTTTTT[G/T]TTTGAGATGGAGTTT	54778
rs74596976	snp	A/G	0.0306436	0.119928	intron-variant	RNF111	GRCh38.p7	15:59058584	GAGGGGAGACTTTTT[A/G]TCATTACTTTCGTTA	54778
rs74645376	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59057623	CTACCTGAAATTTCT[G/T]TTACTTTCTGATAGA	54778
rs74734948	snp	G/T	0	0	intron-variant	RNF111	GRCh38.p7	15:59072468	TTTTTTTTTTTTTTT[G/T]TTTTTGAGACAGCCT	54778
rs74761629	snp	G/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59049386	TTTTTTTTTTTTTTT[G/T]GGCCACCTAGTATGC	54778
rs74781670	snp	A/C	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59071691	CAGAGATCCTGTCGC[A/C]AAAAAAAAAAAAAAT	54778
rs74799576	snp	A/C	0.0287284	0.116357	intron-variant	RNF111	GRCh38.p7	15:59094632	ATATATTATATTGCC[A/C]AGAGTGCTAATTTAA	54778
rs74812098	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59051452	GATTGAGCGAGACTC[-/T]TGTCTCAAAAAAAAA	54778
rs74823333	snp	A/G	0.5	0	intron-variant	RNF111	GRCh38.p7	15:58991291	CAAGACTCCATCTTG[A/G]AAAAAAACAAAACAA	54778
rs74899730	snp	A/T	0.314057	0.241654	intron-variant	RNF111	GRCh38.p7	15:59073492	TCTCCAAAAAAAAAA[A/T]AAATAAATAAACTAC	54778
rs74908426	snp	C/T	0.00517822	0.0506191	intron-variant	RNF111	GRCh38.p7	15:58990276	GGTTTTTGGTATTCA[C/T]TGTTGTGTTTGTCGT	54778
rs74938395	snp	A/G	0.0310518	0.120672	intron-variant	RNF111	GRCh38.p7	15:59006034	TGTATTTCCTTCTAA[A/G]GAAAACCATCTAAAG	54778
rs74975932	snp	C/T	0.130008	0.219321	intron-variant	RNF111	GRCh38.p7	15:59094474	TTATGTGACAGGTAA[C/T]ATACTGCTAACTCCA	54778
rs74976541	snp	A/C	0.040671	0.13668	intron-variant	RNF111	GRCh38.p7	15:59050475	ATTATACCTCAAAAA[A/C]ACTATTTTAAAAAGT	54778
rs75014202	snp	G/T	0	0	intron-variant	RNF111	GRCh38.p7	15:59041978	TTTTTTTTTTTTTTT[G/T]TGCCTGTTTTGATAT	54778
rs75022364	snp	C/G	0.0252325	0.109451	intron-variant	RNF111	GRCh38.p7	15:59018269	TCACATTTGACAATT[C/G]CATTCAAATCTGCTA	54778
rs75070604	snp	C/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59026032	ACTGTGCCCGGCCGG[C/T]TTTTTTTTTTTCTTT	54778
rs75124109	in-del	-/GCCTCTAGAACA			intron-variant	RNF111	GRCh38.p7	15:59005316	GAGCCACTGCACCCA[-/GCCTCTAGAACA]TAGGCTTTCATTACT	54778
rs75160046	in-del	-/G	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59056949	AATTTACACTTTACT[-/G]GGTTAAAAGTATTCC	54778
rs75183178	snp	A/G	0.00755907	0.0610114	intron-variant	RNF111	GRCh38.p7	15:59014120	TGGAGTAGAATTAAT[A/G]CTACATTATTTATTT	54778
rs75216218	snp	G/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59043170	TAATTTTTTTTTTTT[G/T]TTGAGACAGGGTCTC	54778
rs75223286	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59085873	TCACTATATTAATAT[A/G]GATGTTTTAATAGAA	54778
rs75252387	snp	C/T	0.5	0	synonymous-codon	RNF111	GRCh38.p7	15:59066942	CCATTTTCAACATCA[C/T]CACCACCACCACCAT	54778
rs75368214	snp	A/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59071703	CGCAAAAAAAAAAAA[A/T]AATAAAGTTTTTGGA	54778
rs75368859	snp	A/G	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59050157	GAATCTCTTGAACCC[A/G]GGAGGCAGAGGTTGC	54778
rs75373486	snp	C/G	0.5	0	intron-variant	RNF111	GRCh38.p7	15:58989402	CCTGCTCATTTGTTT[C/G]TGACCAAAGATTCAC	54778
rs75479271	snp	A/G	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59041566	ACTCTGTCTCAAAAG[A/G]AAAAAAAAATTACTG	54778
rs75530887	snp	A/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59073493	CTCCAAAAAAAAAAA[A/T]AATAAATAAACTACT	54778
rs75649727	snp	A/G	0.0150606	0.0854603	intron-variant	RNF111	GRCh38.p7	15:59074303	TTGAAGCCAGCCATT[A/G]ACTTCTCTTTGCTAT	54778
rs75688464	snp	C/G/T	0.00319098	0.0398384	intron-variant	RNF111	GRCh38.p7	15:59073522	CTTTCTTTGCTCCTC[C/G/T]GTCAGAAGCAACTCA	54778
rs75701913	snp	A/C	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59078554	GAGAACCTGTCTCTA[A/C]AAAAAAAAAAAAAAA	54778
rs75745360	snp	A/T	0	0	intron-variant	RNF111	GRCh38.p7	15:59007269	CAACCAATGTTCAAT[A/T]TTTTTTTTTTTTTTA	54778
rs75786542	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59024183	CCTAATTTTGTTATT[A/G]TTATTCTCATTCTGC	54778
rs75834274	snp	C/T	0.0341408	0.126114	intron-variant	RNF111	GRCh38.p7	15:59006071	TTTATCTCCAGTAGG[C/T]GTGGTCATTGTCAAG	54778
rs75880969	snp	A/T	0.00953873	0.0683987	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022110	AGTGATCTCCCCGCC[A/T]TGGCCGCCCAAAGTG	54778
rs75885047	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59085875	ACTATATTAATATAG[A/T]TGTTTTAATAGAATT	54778
rs76032918	snp	A/G	0.00755907	0.0610114	intron-variant	RNF111	GRCh38.p7	15:59007710	TTAGTCTTATTGGGT[A/G]TGTAATGGTATATTA	54778
rs76075526	snp	A/G	0.0111196	0.0737302	intron-variant	RNF111	GRCh38.p7	15:59024146	CAATAGTAAATTTTC[A/G]AGAAATCTTAGGTAT	54778
rs76180487	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59067334	TCTTCCCCTTCATTC[C/T]TTCCCTCTCCTTTCT	54778
rs76304702	snp	C/T	0.0166325	0.0896639	intron-variant	RNF111	GRCh38.p7	15:59038233	CACGCACTGACTCCA[C/T]GAGTGATGCATCACT	54778
rs76330301	snp	A/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59077849	GGAAATTTAAATTGT[A/G]TTATTTTCTGTTAGA	54778
rs76410470	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59003015	TGATAAGATCTCATT[A/T]TGTTGCCAGCGCGGG	54778
rs76444199	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59013610	ATTGTGATCAGCTGG[C/T]TGAGTAGTGTTTGCC	54778
rs76526951	snp	A/G	0.0429648	0.14013	intron-variant	RNF111	GRCh38.p7	15:59078043	AATATGGCATAGTAG[A/G]GCACTAGCTTTAGAA	54778
rs76631170	snp	A/T	0.0581099	0.160244	intron-variant	RNF111	GRCh38.p7	15:59061642	TCCTAGTCTCCTAAC[A/T]CCTTCCTTTCCCTTC	54778
rs76638932	snp	G/T	0.0134861	0.0810011	intron-variant	RNF111	GRCh38.p7	15:59014629	GGGAAAGTTGTTAGA[G/T]TCTTCTGTTTTATTC	54778
rs76666814	snp	C/T	0.0644693	0.167566	intron-variant	RNF111	GRCh38.p7	15:59032535	GAAGCCGTCCTCCCA[C/T]GTCAGCGCCTCAAGT	54778
rs76749659	snp	C/G	0.0517044	0.152246	intron-variant	RNF111	GRCh38.p7	15:59062994	AGGCATTGCCAGATA[C/G]TGGGGACAGCATTGC	54778
rs76761339	snp	G/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59002145	CATGGTTGACCATAG[G/T]TAACTGAAACCGTAG	54778
rs76763336	snp	G/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59052593	TTTTTTTTTTTTTTG[G/T]TAAGAGATAGAATAT	54778
rs76812320	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59028390	ATAGTGTTTTTTTTT[C/T]CATATACCTACATGC	54778
rs76880724	snp	A/G	0.0333695	0.124785	intron-variant	RNF111	GRCh38.p7	15:59069413	ATTCATTAAAGAGCT[A/G]CCAAAAGTCTCATTT	54778
rs76886822	snp	G/T	0.0134861	0.0810011	intron-variant	RNF111	GRCh38.p7	15:59032713	TACTATATTCTTGTT[G/T]TTTGCTGTTATCATG	54778
rs76919464	snp	A/T			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986404	TTGKATTTTTAGTAG[A/T]GACAGCGTTTCACCG	54778
rs76936377	snp	A/G	0.0225045	0.103662	intron-variant	RNF111	GRCh38.p7	15:59031859	TTGCAGTATTAAACC[A/G]TGACTCTAATGCTAA	54778
rs76962534	snp	A/G	0.0460142	0.144533	intron-variant	RNF111	GRCh38.p7	15:59039590	ACATCTTCAAACTGG[A/G]TCATTGTCCTTTTGA	54778
rs76969243	snp	A/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59051308	AATAAACAAAAAAAA[A/T]TTAGCTGGGCCTGGT	54778
rs76979606	snp	A/G	0.00243761	0.0348262	synonymous-codon	RNF111	GRCh38.p7	15:59085689	AGCTGGAGTGACTGC[A/G]GCTACTTATACACCT	54778
rs77134451	snp	A/G	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59083155	GCTTAAAAAAAAAAA[A/G]AAGCAAAAAATGAAT	54778
rs77138536	snp	A/G	0.0197687	0.0974348	intron-variant	RNF111	GRCh38.p7	15:59009597	TATAGAACGATACCA[A/G]AATTAGAACTTGGAG	54778
rs77163081	snp	A/G	0.0134861	0.0810011	intron-variant	RNF111	GRCh38.p7	15:59023603	GTTTTCTACTATTGA[A/G]CTCATTTGTCAGTGT	54778
rs77177655	snp	A/G	0.00835141	0.0640778	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021626	AATTTTATGAGGTAA[A/G]TACTATTATTATTCC	54778
rs77180945	snp	A/G/T	0.00836019	0.0642129	intron-variant	RNF111	GRCh38.p7	15:59027298	CCCCAGCTGTTTCCA[A/G/T]CATACATCATGAGAC	54778
rs77274335	snp	A/G	0.120326	0.21374	intron-variant	RNF111	GRCh38.p7	15:59014125	TAGAATTAATACTAC[A/G]TTATTTATTTTGTTG	54778
rs77337694	snp	C/T	0.0115144	0.0749975	intron-variant	RNF111	GRCh38.p7	15:59057508	TTCAGATTTAATTGT[C/T]GTGACTATGCTTTGG	54778
rs77391394	in-del	-/TT			intron-variant	RNF111	GRCh38.p7	15:59027850	CCTTTTTTTTTTTTT[-/TT]CCCCACTCTTGTTGT	54778
rs77397955	snp	G/T	0.00478085	0.0486577	intron-variant	RNF111	GRCh38.p7	15:59073581	TCAATCACATCTTCA[G/T]GTTCCAACTTCTTAT	54778
rs77425411	snp	A/G	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59078883	AAAAAAAAAAAAAAA[A/G]AGAGGTATAGGTAAG	54778
rs77443443	snp	G/T	0.000512138	0.015994	missense	RNF111	GRCh38.p7	15:59076010	TCATGGAAGTGGCAG[G/T]TTTCATGGAGCATCT	54778
rs77521626	snp	C/T	0.0383715	0.133092	intron-variant	RNF111	GRCh38.p7	15:59038070	AATGTTAATTTAGAG[C/T]TAGTGATTATTACCC	54778
rs77605367	snp	A/C	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:59011396	ATTCTTGTGTTTACA[A/C]TACTTGGGGCATTCT	54778
rs77629502	snp	A/G	0.0130921	0.0798413	intron-variant	RNF111	GRCh38.p7	15:59081364	CAACTCTGAAATCCA[A/G]CTAGGCATGGTGGCA	54778
rs77633060	snp	C/T	0.0748431	0.178382	intron-variant	RNF111	GRCh38.p7	15:59051092	CTAATTTAATACTTA[C/T]CCATCTTCTAAATAA	54778
rs77671722	snp	A/C	0.0452528	0.143452	intron-variant	RNF111	GRCh38.p7	15:59026268	TTACTAAATCCCAAC[A/C]CTAATTTTTAGTTTT	54778
rs77678884	snp	A/C	0.0341408	0.126114	intron-variant	RNF111	GRCh38.p7	15:58998547	TGATTTAGTTATAAA[A/C]TGGATTAGCAAACTA	54778
rs77692481	snp	C/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59071373	GGTGAAAGTGTTTTG[C/T]TTAGGATTTTTCCAG	54778
rs77708856	snp	G/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59045206	CTTTTTTTTTTTTTT[G/T]AGACAGAGTTTTTGT	54778
rs77715716	snp	A/G	0.0185938	0.0946107	intron-variant	RNF111	GRCh38.p7	15:59054949	GACTGCATATTCTAC[A/G]TATTATCCCTGTATG	54778
rs77730322	snp	A/G	0.00716266	0.059414	intron-variant	RNF111	GRCh38.p7	15:59060914	TCAAGTGATCCTCCC[A/G]AGTAGATGGGGGACC	54778
rs77768153	snp	C/G	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59023828	AAACAAACCATGTCT[C/G]TGAGCTGAATCCTGC	54778
rs77949022	snp	C/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59011524	AAAACTTTACTTACT[C/T]CTAGTTCTGTAGAGT	54778
rs77978639	snp	A/T	0.00874735	0.0655527	intron-variant	RNF111	GRCh38.p7	15:59060810	ATTATTATTATTATT[A/T]TTTTTTTTGTGAGAC	54778
rs77985842	snp	A/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:58994056	TTTTTTTTTTTTTTT[A/T]TAATGGAGTCTCACT	54778
rs78004728	snp	A/T	0	0	intron-variant	RNF111	GRCh38.p7	15:59037001	ACTACAGTTGACTAA[A/T]TTTTTTTTTTTTTTT	54778
rs78129489	snp	C/T	0	0	intron-variant	RNF111	GRCh38.p7	15:58989876	TAGATGTTTCCTTCT[C/T]TTTTTTTTTGTTATA	54778
rs78137055	snp	A/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:58994059	TTTTTTTTTTTTTTA[A/T]TGGAGTCTCACTCTG	54778
rs78245646	snp	C/T	0.00716266	0.059414	intron-variant	RNF111	GRCh38.p7	15:59029973	CCTTTCTGATTAATA[C/T]ATTTCATTTTGAGTC	54778
rs78252119	snp	A/G	0.0279526	0.114869	intron-variant	RNF111	GRCh38.p7	15:59064156	TTTAACACTTGACCA[A/G]GTTATTCAACACATT	54778
rs78271469	snp	C/T	0.030665	0.119967	intron-variant	RNF111	GRCh38.p7	15:59063153	CTACATGATTGCATG[C/T]TGCTTTTCCCTTGTG	54778
rs78293059	snp	A/G/T	0.0345262	0.126772	intron-variant	RNF111	GRCh38.p7	15:59023702	TTACTAGCCTTTCCA[A/G/T]AAGAATGTTTTATAA	54778
rs78352043	snp	A/C	0.48155	0.0942576	intron-variant	RNF111	GRCh38.p7	15:59072894	TTAAAAAAAAAAAAA[A/C]AAAACACTTCCAGCT	54778
rs78464076	snp	C/T	0.0383715	0.133092	intron-variant	RNF111	GRCh38.p7	15:59045904	TAGCCACTTGGGTGC[C/T]ACTGTTTTGTTGTTT	54778
rs78471398	snp	A/G	0.0663309	0.169604	intron-variant	RNF111	GRCh38.p7	15:59069056	TCCAGCCTTGGCGAC[A/G]GAACAAGACTCCGTC	54778
rs78549597	snp	A/C	0	0	intron-variant	RNF111	GRCh38.p7	15:59000710	CTGAACTCCGTCTCA[A/C]AAAAAAAAAAAAAAG	54778
rs78617576	snp	A/G	0.156319	0.231784	intron-variant	RNF111	GRCh38.p7	15:58990090	AAATAATATAGGGCT[A/G]AGGACAGGAGATCTA	54778
rs78627099	snp	A/G	0.0279526	0.114869	intron-variant	RNF111	GRCh38.p7	15:59009633	GTGAGTGAGTGTCCA[A/G]AATATTACCCAGTAA	54778
rs78637059	snp	A/T	0.0349115	0.127424	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022199	AATATTTTATAAGAC[A/T]AATTAACCTTGAAAT	54778
rs78654663	snp	C/T	0.0228947	0.104514	intron-variant	RNF111	GRCh38.p7	15:59012061	GCTCTGTCACCCAGG[C/T]GGGAATGCAGTGAGT	54778
rs78694748	snp	A/G	0.00716266	0.059414	intron-variant	RNF111	GRCh38.p7	15:59019297	TAATGAGAAAATGCA[A/G]ACAATATTACTTTGA	54778
rs78714746	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59089939	TTAATCTTAGGGTCA[A/G]AAGTTACCGAAATAT	54778
rs78720477	in-del	-/TTT			intron-variant	RNF111	GRCh38.p7	15:58998257	AAGTTTTTTTTTTTT[-/TTT]AAGTTTAAGTTCAGG	54778
rs78754862	snp	A/C	0.0279526	0.114869	intron-variant	RNF111	GRCh38.p7	15:59065331	AATGAATTTGAAACA[A/C]TGGGACAGACTTTCA	54778
rs78759923	snp	A/G	0.0341408	0.126114	intron-variant	RNF111	GRCh38.p7	15:59011156	GAAACTCTGCCATGA[A/G]AAATAGGGTAATTGG	54778
rs78775489	snp	C/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59042101	TTAATTAGTAGTTTC[C/T]TGACTTACATACTTT	54778
rs78784943	snp	A/G	0.0279526	0.114869	intron-variant	RNF111	GRCh38.p7	15:59072208	GTACCTAAAGATTGG[A/G]GTGGCTGTGGCAATT	54778
rs78850439	snp	C/T	0.0142736	0.0832652	intron-variant	RNF111	GRCh38.p7	15:59074312	GCCATTGACTTCTCT[C/T]TGCTATGAAAGTCCT	54778
rs78935570	snp	A/G	0.0165278	0.0893908	intron-variant	RNF111	GRCh38.p7	15:59028720	TGAATATGTGTTTTC[A/G]TTTCTCTTGGGTACA	54778
rs78949317	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59078070	AGAATTGGATAGATT[C/T]GAGTTGACCTCCCAG	54778
rs79043409	snp	A/C	0.0267878	0.112589	utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58988023	CTTCCTTCCTGGGTC[A/C]GTGATTCCCGGACCC	54778
rs79057769	snp	C/T	0.0456336	0.143994	intron-variant	RNF111	GRCh38.p7	15:59012500	TGTATGCTTTGTGTA[C/T]GTATTGACTATTAAT	54778
rs79059603	snp	A/G	0.0670745	0.170406	intron-variant	RNF111	GRCh38.p7	15:59001322	CTTTGATAACTTCTT[A/G]GCCATTTTTTACCTC	54778
rs79063327	snp	C/T	0.0463947	0.145069	intron-variant	RNF111	GRCh38.p7	15:59034259	TGCTGCATTGAGCAA[C/T]ATTGTGCTTGCGTTT	54778
rs79066476	snp	A/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59029592	GGAGACCTGTAAGAT[A/T]ATATATTTCTGTAAC	54778
rs79069331	snp	C/T	0.00597247	0.0543191	intron-variant	RNF111	GRCh38.p7	15:59001341	ATTTTTTACCTCTCT[C/T]CTCTTTTCTGGATTT	54778
rs79091558	snp	A/G	0.0872718	0.189788	intron-variant	RNF111	GRCh38.p7	15:58991576	AGATTGAGTGGTTAG[A/G]GAGGGCCTTTTTAGA	54778
rs79302878	snp	A/C	0.0391387	0.134304	intron-variant	RNF111	GRCh38.p7	15:59013321	CATGACTAAGAGACC[A/C]ACATTGATACATCAC	54778
rs79302950	snp	G/T	0	0	intron-variant	RNF111	GRCh38.p7	15:59058140	GAATAAGCATATCGG[G/T]GTTGGATTTTTTTAA	54778
rs79321970	snp	A/G	0.0185938	0.0946107	intron-variant	RNF111	GRCh38.p7	15:59009977	ACAAACAAAAATTAA[A/G]ATGATTTTGCTAAAT	54778
rs79341960	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59085874	CACTATATTAATATA[A/G]ATGTTTTAATAGAAT	54778
rs79347638	in-del	-/TTT			intron-variant	RNF111	GRCh38.p7	15:59041977	TTTTTTTTTTTTTTT[-/TTT]GCCTGTTTTGATATC	54778
rs79352787	snp	C/T	0.0205511	0.0992634	intron-variant	RNF111	GRCh38.p7	15:59054649	ACTCCTTCTTAAGAA[C/T]TTTATTTTAGAATTT	54778
rs79360144	snp	A/C	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59069075	CAAGACTCCGTCTCA[A/C]AAAAAAAAAAAAAAA	54778
rs79401035	snp	A/G	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59061458	GATCAGTTCCCTTTC[A/G]TTCCTCTAAGTGCCT	54778
rs79463862	snp	C/G	0.0228947	0.104514	intron-variant	RNF111	GRCh38.p7	15:59047130	GCCTGGCCAGGAATT[C/G]TTATAATTCAACAAT	54778
rs79464006	snp	C/T	0.0648419	0.167978	intron-variant	RNF111	GRCh38.p7	15:59070938	AACATCAGATCTTTA[C/T]GATCTTTCATCACAT	54778
rs79526707	snp	A/C	0.105924	0.204309	intron-variant	RNF111	GRCh38.p7	15:59000017	AATCCAGTCACCTCC[A/C]GGCAGGCCCCACCTC	54778
rs79654854	snp	G/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59037016	TTTTTTTTTTTTTTT[G/T]GGTAGAGACAGGGTT	54778
rs79685667	snp	A/G	0.0995161	0.199636	intron-variant	RNF111	GRCh38.p7	15:59018330	TATTCTGTCATTAAG[A/G]TGTCCAGGATTGGTG	54778
rs79726847	snp	A/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59078552	GTGAGAACCTGTCTC[A/T]AAAAAAAAAAAAAAA	54778
rs79740936	snp	C/T	0.021333	0.101051	intron-variant	RNF111	GRCh38.p7	15:58993819	TCCTGAGGGCATACA[C/T]GATTAGCATCTTAGT	54778
rs79757484	snp	A/G	0.00755907	0.0610114	intron-variant	RNF111	GRCh38.p7	15:59029899	ACTTGTTAAAAATAT[A/G]TTAACATTGTTTATT	54778
rs79780805	snp	A/C	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59071690	ACAGAGATCCTGTCG[A/C]AAAAAAAAAAAAAAA	54778
rs79782996	snp	A/C	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59032219	GATGGGATTACAGGC[A/C]TGAGCCACTGTACCT	54778
rs79792215	snp	A/G	0.067446	0.170804	intron-variant	RNF111	GRCh38.p7	15:59041112	GAGGAATGAAAGTAT[A/G]TATCTCCGTATATCT	54778
rs79796857	snp	C/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59026033	CTGTGCCCGGCCGGC[C/T]TTTTTTTTTTCTTTT	54778
rs79798648	in-del	-/AA/G	0.00597247	0.0543191	intron-variant	RNF111	GRCh38.p7	15:59002567	AATTAAAAAAAAAAA[-/AA/G]GAGAGAGAGTGACCA	54778
rs79832363	snp	C/T	0	0	intron-variant	RNF111	GRCh38.p7	15:59012004	TTTTGTTTGTTTGCC[C/T]TTTTTTTTTTTTTTT	54778
rs79857477	snp	A/G	0.0696718	0.173152	intron-variant	RNF111	GRCh38.p7	15:59053008	AAATTAAAAATGAAA[A/G]AATATTAAGGGGTAT	54778
rs79870691	snp	C/G	0.0178098	0.0926698	intron-variant	RNF111	GRCh38.p7	15:59018403	TCCTGTAAAAATTGT[C/G]CTTGCATATATTTGA	54778
rs79948863	snp	A/G	0	0	intron-variant	RNF111	GRCh38.p7	15:59078880	AGAAAAAAAAAAAAA[A/G]AAGAGAGGTATAGGT	54778
rs79978926	snp	A/G	0.00636936	0.0560724	intron-variant	RNF111	GRCh38.p7	15:59002567	AATTAAAAAAAAAAA[A/G]AGAGAGAGAGTGACC	54778
rs79990266	snp	C/T	0.0626037	0.165477	intron-variant	RNF111	GRCh38.p7	15:59082698	ACAACAGAGAACATA[C/T]GGCCTGTAGAGCTGA	54778
rs80003295	snp	A/G	0.0166325	0.0896639	intron-variant	RNF111	GRCh38.p7	15:59093712	TGCCATATGAAACAG[A/G]TTCTATATCATATAT	54778
rs80010324	snp	G/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59012033	TTTTTTTTTTTTTTT[G/T]AGATGGAGTCTCGCT	54778
rs80069580	snp	A/G	0.0410537	0.137264	intron-variant	RNF111	GRCh38.p7	15:59067407	GAAAACCCAGCATGA[A/G]GGAGTAACTACTTGC	54778
rs80078459	in-del	-/TT			intron-variant	RNF111	GRCh38.p7	15:59062075	TTTTTTTTTTCCCCG[-/TT]AGACAGGGTCTTGCT	54778
rs80083708	snp	A/G/T	0.0452528	0.143452	intron-variant	RNF111	GRCh38.p7	15:59026211	GATAGTCTTAATGGG[A/G/T]TTTTCCTCCTTTTGC	54778
rs80134747	snp	A/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59051310	TAAACAAAAAAAAAT[A/T]AGCTGGGCCTGGTGG	54778
rs80141555	snp	C/T	0.5	0	missense	RNF111	GRCh38.p7	15:59081094	TCTCATGCAACATCT[C/T]ATCCTGTGGCACCCC	54778
rs80153747	snp	A/G	0.0505692	0.150756	intron-variant	RNF111	GRCh38.p7	15:58989170	ATCTTTTGATAGTTT[A/G]TTACTATATGTATTT	54778
rs80161405	snp	A/T	0.0263992	0.111815	intron-variant	RNF111	GRCh38.p7	15:59088010	TATAGCCTTCTTGCT[A/T]TATAAGCTTGGCTGT	54778
rs80164809	snp	C/G	0.00517822	0.0506191	intron-variant	RNF111	GRCh38.p7	15:59059819	TTGCTAACTGCTTAC[C/G]AATAGGGACACTGTA	54778
rs80192488	snp	C/T	0.0111196	0.0737302	intron-variant	RNF111	GRCh38.p7	15:59064739	CCCCCATAGGCCAGA[C/T]TAGCAGCTTGGAAAA	54778
rs80228731	in-del	-/TTG			intron-variant	RNF111	GRCh38.p7	15:59000180	TTTTTTTTTTTTTTT[-/TTG]AGACAGGGTCTCTCT	54778
rs80271276	snp	C/T	0.0704125	0.17392	intron-variant	RNF111	GRCh38.p7	15:59036826	TCATTTGTGGTTCTT[C/T]TTGGTTTGGTTTTAT	54778
rs80291252	snp	C/T	0.0418186	0.138422	intron-variant	RNF111	GRCh38.p7	15:59014296	GTGAAATCAGCTGTT[C/T]TGCCAAGAAACCTTT	54778
rs111286540	snp	C/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:58994760	TGGGGTGAGCCTTTG[C/T]GCCTGGCCCCTTATT	54778
rs111330212	snp	C/T	0.00118923	0.024356	missense	RNF111	GRCh38.p7	15:59066797	CATCTAGTGCTGTAA[C/T]GGAAACTGGCCCTCC	54778
rs111378251	snp	C/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59054961	TACATATTATCCCTG[C/T]ATGTCCTTAGTCCAA	54778
rs111430438	snp	A/G	0.0422008	0.138995	intron-variant	RNF111	GRCh38.p7	15:59029018	CTCCTGGCCTCCAGT[A/G]ATCCGCCCGCCTTGG	54778
rs111440124	snp	A/G	0.0637235	0.166737	intron-variant	RNF111	GRCh38.p7	15:59036351	CAGGTTTGAGCCACC[A/G]CACCCGGCCAAGACT	54778
rs111463749	snp	A/C	0.5	0	utr-variant-3-prime	RNF111	GRCh38.p7	15:59097128	GATAAGTAATGAAGA[A/C]AGTAAGGAAGAAAAT	54778
rs111491282	snp	C/T	0.0337553	0.125452	intron-variant	RNF111	GRCh38.p7	15:59039599	AACTGGGTCATTGTC[C/T]TTTTGATGCCATCCT	54778
rs111501184	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59023540	TATTTTTATTTATAT[A/T]TTTTTGGTAAATATA	54778
rs111614486	snp	C/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59069388	AGGTGGGTCTACCAG[C/T]TTTTCCTACATTCAT	54778
rs111635288	snp	G/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59010832	ATGTTGAAGATTAAA[G/T]GAGAGCCTGTGGTTT	54778
rs111639395	snp	C/G	0.5	0	intron-variant	RNF111	GRCh38.p7	15:58994769	CCTTTGCGCCTGGCC[C/G]CTTATTCTCTCTTGA	54778
rs111720953	snp	C/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59014567	GTTCTTAAGAAGTTA[C/G]AAAGCTTCAGAAGAA	54778
rs111732323	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:58993369	CAAAAATAAAAAAAA[A/T]ATAACTGTAAATACA	54778
rs111757184	snp	A/G	0.0126979	0.078662	intron-variant	RNF111	GRCh38.p7	15:59008770	CATATTACATTTATC[A/G]CCACTTTTGGCTTAT	54778
rs111764087	snp	C/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59039488	GAGTATCATTATGAA[C/T]GCATGAATTTTAGTA	54778
rs111818111	snp	C/T	0.0126979	0.078662	intron-variant	RNF111	GRCh38.p7	15:58998739	AAGCAAAAATTAGAA[C/T]TGTGGAAAACGCCTA	54778
rs111822217	snp	C/G	0.021333	0.101051	intron-variant	RNF111	GRCh38.p7	15:59046529	GTATATTCATATGCA[C/G]AAAAGATAAATTTAG	54778
rs111907812	snp	C/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59089483	TTTTGGAGAGTTAGG[C/T]TATATTTTAACAGAA	54778
rs111911587	snp	A/G	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59051471	TCAAAAAAAAAAAGG[A/G]AAAAAAAAAAAAGAC	54778
rs111922375	snp	G/T	0.0704125	0.17392	intron-variant	RNF111	GRCh38.p7	15:59028021	TAGTAGAGATGGGGT[G/T]TCACCATGTTGGCCA	54778
rs111959653	snp	A/C	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59072709	TGCCTGCCTCAGCCT[A/C]CCAAAGTGCTGGGAT	54778
rs112016203	snp	C/T	0.150333	0.229274	intron-variant	RNF111	GRCh38.p7	15:58999427	TGCAATCTCCGCCCC[C/T]CAGGTTCAAGCAATT	54778
rs112016720	snp	G/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59087702	GAGTAAGCTGAAGAG[G/T]AGGAAAAGGAGGGAT	54778
rs112038985	snp	C/G	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59012661	TTCTCAGTGTATACA[C/G]ATGTATGTCTTGCTA	54778
rs112051063	snp	C/T	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:59056063	TGATAGCTATTTTCT[C/T]AGGAAAAAATATTTT	54778
rs112065402	snp	A/C	0.021333	0.101051	intron-variant	RNF111	GRCh38.p7	15:59044369	CATCATTCCAGTCTT[A/C]AGGCACAGAGAGACT	54778
rs112069574	snp	A/G	0.0547245	0.156101	intron-variant	RNF111	GRCh38.p7	15:59060415	TCAAGACCAGCCTAG[A/G]CAACGTGGTGAAACC	54778
rs112077574	snp	A/C	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59015886	TATTCGAGACAGGTT[A/C]TCACGCCCAGGTTGG	54778
rs112129861	snp	C/G	0.116488	0.211364	intron-variant	RNF111	GRCh38.p7	15:59047450	CAGTGAGCTATTATC[C/G]TGCCATTGTACTCCA	54778
rs112156647	snp	C/T	0.0126979	0.078662	intron-variant	RNF111	GRCh38.p7	15:59018782	TTGTACAAATCCTGC[C/T]TGATTTTAAAAGGCT	54778
rs112180296	snp	A/G	0.0267878	0.112589	intron-variant	RNF111	GRCh38.p7	15:59051675	TTGAGAGGCTGAGGC[A/G]TGAGAATCACTTGAA	54778
rs112213044	snp	G/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59064934	CACCCCCCTACCCAG[G/T]TTCATTTATGTGAAC	54778
rs112241669	snp	C/G	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59059478	GTTAAAATAGAGTTA[C/G]CATTGGATGCACTAA	54778
rs112314859	snp	A/G	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59050903	TAACTGAAAATTAGA[A/G]GAGGTATCAAAAATT	54778
rs112323787	snp	C/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59027205	GTCTAATTTTTAAAT[C/T]TTCAGCCCATAAAGA	54778
rs112339112	snp	C/T	0.0130921	0.0798413	intron-variant	RNF111	GRCh38.p7	15:59090135	AATTCCCTTTGTAGC[C/T]AAATGTCTTGTTTGA	54778
rs112357033	snp	A/T	0.021333	0.101051	intron-variant	RNF111	GRCh38.p7	15:59078156	CATTCTTTGCACTTG[A/T]AAAATGGGAATAATT	54778
rs112425141	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59085810	AAAATTTTCAAAATT[G/T]TGACATGTTCTAAAA	54778
rs112434328	snp	A/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59012360	GGTAATTACAGTATT[A/T]GATAATTAAGACCCT	54778
rs112497414	snp	A/G	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59088332	TAAGTGAAGATTTAG[A/G]TAATTTGGGATGCAG	54778
rs112595522	snp	C/T	0.0146672	0.084371	intron-variant	RNF111	GRCh38.p7	15:59071150	AGTATACAAAAAAAG[C/T]AGCCGGGCGTGGTGG	54778
rs112656959	snp	C/T	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59035625	TGCTCTGCTTCCTCT[C/T]GAATGGTTTGCTCTT	54778
rs112657167	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59039826	GGTTCAAGCGATTCC[C/T]CTGCCTCAGCCTCCT	54778
rs112696327	snp	C/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59074569	TTGCCTCCCTCAGCC[C/T]TCATAGAATTGAAGA	54778
rs112702214	snp	A/G	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59085427	TTTGTAAGATGTGAA[A/G]CCAAGTAGAAATGCT	54778
rs112777753	snp	A/G	0.5	0	intron-variant	RNF111	GRCh38.p7	15:58999907	GGAGAGAAGGGGGAA[A/G]TGCCACACAATTTTA	54778
rs112835635	snp	A/G	0.0185938	0.0946107	intron-variant	RNF111	GRCh38.p7	15:59059790	TTTTTGGATAATGGT[A/G]CAGAGATAGGAACTT	54778
rs112958194	snp	C/G	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59074633	AAGAGAATATTGTAG[C/G]TGGTTTGATCTTCCA	54778
rs112968854	snp	C/G	0.0115144	0.0749975	utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58987672	AGCCCTAGTGTCGTG[C/G]TCTCCTCGGTAGGGG	54778
rs112972758	snp	C/T	0.0955749	0.196603	intron-variant	RNF111	GRCh38.p7	15:59008417	AGAGACAGGGTCTCA[C/T]TTTATTGCCCAGGCT	54778
rs112982532	snp	A/G	0.120326	0.21374	intron-variant	RNF111	GRCh38.p7	15:59044376	CCAGTCTTAAGGCAC[A/G]GAGAGACTAAGGTGA	54778
rs113047964	snp	A/G	0.0126979	0.078662	intron-variant	RNF111	GRCh38.p7	15:58999400	GAGTGCAGTGGTGCA[A/G]TCTCAGTTCACTGCA	54778
rs113077756	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:58997773	GTGAGCCAAGATTGC[A/G]CCACTGCACTCCAGC	54778
rs113083442	snp	C/G	0.0883596	0.190715	intron-variant	RNF111	GRCh38.p7	15:59080367	TTCAGGTGACTCTGC[C/G]CACCTTGGCCTCCTA	54778
rs113094872	snp	C/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59066331	TATGGCACTATCAGC[C/T]GGGGTGTGGTGGCTC	54778
rs113105798	snp	A/G	0.0185938	0.0946107	intron-variant	RNF111	GRCh38.p7	15:59009261	ACTGCGCCTGGCCAC[A/G]TATTTTACTTTTACA	54778
rs113110238	snp	A/G	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59051469	TCTCAAAAAAAAAAA[A/G]GAAAAAAAAAAAAAG	54778
rs113111519	snp	C/T	0.0126979	0.078662	intron-variant	RNF111	GRCh38.p7	15:59027851	CTTTTTTTTTTTTTT[C/T]CCCCACTCTTGTTGT	54778
rs113137848	snp	C/T	0.107341	0.205301	intron-variant	RNF111	GRCh38.p7	15:59032114	CAGCTAATTTTTGTA[C/T]TTTTAGTGGAGACGG	54778
rs113151179	snp	C/T	0.00636936	0.0560724	intron-variant	RNF111	GRCh38.p7	15:59083107	TGAGCTATGATTGTG[C/T]CACTGCACTTGATCC	54778
rs113187300	snp	C/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59060338	CTTGACATGGTGAGA[C/T]TCACACCTGTAATCC	54778
rs113200452	snp	C/T	0.000247221	0.0111153	missense	RNF111	GRCh38.p7	15:59076147	GATCAAGCATGGTTG[C/T]GCAGCCCCAGCCCCA	54778
rs113202002	in-del	-/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59039721	TTTAAGAACTCCTGA[-/T]TTTTTTTTTTTTTTG	54778
rs113269835	snp	C/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59089326	GAAGTAAAAAACTTA[C/T]CTTGAAGTCGAATTT	54778
rs113289083	snp	A/G	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59014521	TTCTGCTGTGGAATT[A/G]TAGAAAGCAGCTTTT	54778
rs113318416	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59050608	AACTGCATTATTGAG[A/G/T]TATGATTAGTATACT	54778
rs113356160	snp	C/G	0.0333695	0.124785	intron-variant	RNF111	GRCh38.p7	15:59059474	GAAAGTTAAAATAGA[C/G]TTACCATTGGATGCA	54778
rs113435050	snp	C/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59063331	AGTGCCTTTTGTAGA[C/T]CTTTTACCACGACTT	54778
rs113436753	snp	A/G	0	0	intron-variant	RNF111	GRCh38.p7	15:59045869	TAATTTGGAAATTCA[A/G]TCTACAATATTATTT	54778
rs113507414	snp	A/C	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59053964	TTTTTGAGACAGAGT[A/C]TCCCTCTGTCACCCA	54778
rs113557350	in-del	-/T	0.5	0	downstream-variant-500B	RNF111	GRCh38.p7	15:59097537	TGACTTTATTTTAGC[-/T]GCTAGCACACTTCAG	54778
rs113589308	snp	A/C	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59034276	TTGTGCTTGCGTTTT[A/C]TACACCTATGTAAGT	54778
rs113690614	snp	A/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59089234	AAAAAATTAGAAAAC[A/T]GTGTTAAAAGTTTCC	54778
rs113710080	snp	C/T	0.5	0	intron-variant, missense	RNF111	GRCh38.p7	15:59022585	TATCCCTTGTGCAGT[C/T]CTCTTTTAACAAGTA	54778
rs113711750	snp	C/G	0.5	0	intron-variant	RNF111	GRCh38.p7	15:58997691	CGTGGTGGCATATGT[C/G]TGTAATCCCAGCTAC	54778
rs113712807	snp	A/G	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59063389	GAGTAATTCATGCCT[A/G]CCTCTCGATAATCCT	54778
rs113771587	snp	A/G	0.00021664	0.0104054	intron-variant	RNF111	GRCh38.p7	15:59091170	GTAAGAATTTATTCT[A/G]TGAAACTTCTGGAGT	54778
rs113790785	snp	A/G	0.444444	0.157135	intron-variant	RNF111	GRCh38.p7	15:59052600	TTTTTTTGGTAAGAG[A/G]TAGAATATTGCTATG	54778
rs113856720	snp	A/G	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59057734	GGAAAGGAGATTAAA[A/G]CAGTTATTGGAAATC	54778
rs113862733	in-del	-/TTCTTGTCAGGCTG	0.494774	0.0508504	intron-variant	RNF111	GRCh38.p7	15:59019557	TGGGTTTATACACCA[-/TTCTTGTCAGGCTG]TTCTTGTCAGGCTTA	54778
rs113892976	snp	C/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59085534	TTTTGGGCTAAATTA[C/T]CTTTCCTCAGCTTTG	54778
rs113935303	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59020124	ATATTTCATATATAA[A/G]ATACATATTTTATAT	54778
rs113972620	snp	G/T	0.0618563	0.164627	intron-variant	RNF111	GRCh38.p7	15:59086146	TTTTTTTTCGACAGA[G/T]TCTCACTCTGTCACC	54778
rs114020592	snp	A/G	0.0341408	0.126114	intron-variant	RNF111	GRCh38.p7	15:59023351	CCCATAAATTTTTGC[A/G]TAACTGACATTGTTA	54778
rs114020934	snp	C/G	0.0663309	0.169604	intron-variant	RNF111	GRCh38.p7	15:59001677	AGAAAATACTTAATA[C/G]TTTTATTAAGTGAAG	54778
rs114021668	snp	C/T	0.0123036	0.0774623	intron-variant	RNF111	GRCh38.p7	15:59057222	AGTGCACATCTCCTC[C/T]CCAGCGAACAAAAAA	54778
rs114193479	snp	A/C	0.0248432	0.108648	intron-variant	RNF111	GRCh38.p7	15:59061256	GGCCTCTCTTAAGGT[A/C]AATTTCCTTCCAGGA	54778
rs114239946	snp	A/G	0.0887219	0.191022	intron-variant	RNF111	GRCh38.p7	15:59082349	CGTGTGGTAAAAATC[A/G]GTGTTAAAATTGATG	54778
rs114299679	snp	C/T	0.0168055	0.0901129	intron-variant	RNF111	GRCh38.p7	15:59078089	TTGACCTCCCAGCTC[C/T]GACTAATTAGCTTGG	54778
rs114344379	snp	C/T	0.0452528	0.143452	intron-variant	RNF111	GRCh38.p7	15:59067824	CTACTGTAGAGTTCA[C/T]TATAACCTTCACTCA	54778
rs114412655	snp	C/T	0.0115144	0.0749975	intron-variant	RNF111	GRCh38.p7	15:58992551	GGCTGGGCCCAGTGG[C/T]TCATGCCTGTAATCA	54778
rs114422424	snp	C/T	0.00874735	0.0655527	intron-variant	RNF111	GRCh38.p7	15:59052156	GTGTGTTTTTTGTTC[C/T]TTGTGTATTTTTTTA	54778
rs114426472	snp	A/G	0.0410537	0.137264	intron-variant	RNF111	GRCh38.p7	15:59018488	ATTTAAATATATTAT[A/G]TTCTCATAATTTATT	54778
rs114466785	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59029595	GACCTGTAAGATTAT[A/G]TATTTCTGTAACCCA	54778
rs114488646	snp	A/G	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:58998430	GAAAGATTACAGTGA[A/G]TGTTCTTCCCCTCAT	54778
rs114510134	snp	C/T	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:58988744	ATTATTCAAAAAATA[C/T]CAGAAAGTATGAGGT	54778
rs114523413	snp	A/C	0.00874735	0.0655527	intron-variant	RNF111	GRCh38.p7	15:59063883	AAGGTAATTTAGCGT[A/C]TCCCAGTGAGTGAGC	54778
rs114528459	snp	C/G	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:59069573	ATATAACTCGTTTAC[C/G]CACCTGTAAGTATTA	54778
rs114591874	snp	C/G	0.0528381	0.153711	intron-variant	RNF111	GRCh38.p7	15:59088761	TTATGTGTGTTTCTG[C/G]TTAAAGACAACTTTA	54778
rs114608812	snp	C/T	0.00993419	0.0697739	upstream-variant-2KB	RNF111	GRCh38.p7	15:58986135	ATGCTCTTTTAGTTT[C/T]CCCACACAATCTGCT	54778
rs114632252	snp	A/G	0.0126979	0.078662	intron-variant	RNF111	GRCh38.p7	15:59039453	GTTCTAGCAGCATCC[A/G]AAGAGGTTTTTTCAC	54778
rs114651370	snp	C/G/T	0.0115206	0.075079	intron-variant	RNF111	GRCh38.p7	15:59042377	AGTGATCCACCCGCT[C/G/T]GGCCTCACAAGGTGC	54778
rs114795940	snp	A/T	0.0376037	0.131863	intron-variant	RNF111	GRCh38.p7	15:58997061	TTTTACTTAGTTTTC[A/T]TGTCAGTTTAAGTGT	54778
rs114812703	snp	A/C	0.00795532	0.062565	intron-variant	RNF111	GRCh38.p7	15:59015141	TACTAGGACCAAAGT[A/C]GAATTTTTTAAATTC	54778
rs114901638	snp	A/C	0.000783239	0.0197739	intron-variant	RNF111	GRCh38.p7	15:59093455	GGCTGAAGCGATCCA[A/C]CTACCTCAGCCTCCC	54778
rs115010772	snp	C/T	0.00835141	0.0640778	intron-variant	RNF111	GRCh38.p7	15:59057542	GATTTATTCCTACCG[C/T]TCTCAATTTTAAGCA	54778
rs115014341	snp	A/T	0.00478085	0.0486577	intron-variant	RNF111	GRCh38.p7	15:59063368	GTGTAAGACTGTTGA[A/T]TGAATGAGTAATTCA	54778
rs115033971	snp	C/G	0.0154538	0.0865337	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096748	TTACTGGGGAAAAGA[C/G]CAAGTAGCCTGTCTT	54778
rs115053972	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59049630	TTTGGCAAGAATTTC[A/G]TTTGTTACAGCATTG	54778
rs115216199	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	RNF111	GRCh38.p7	15:58987284	GTGAGGTGCCGTGAT[C/T]TTTATGTCATTAGCG	54778
rs115227518	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59087760	GGTGGCAGAAAATCT[A/G]CATGTAAGCAGACCC	54778
rs115256142	snp	C/T	0.0103295	0.0711199	upstream-variant-2KB	RNF111	GRCh38.p7	15:58986840	GCTTACTGAATGATA[C/T]GGAAAATATGAGTGA	54778
rs115307273	snp	C/T	0.0670745	0.170406	intron-variant	RNF111	GRCh38.p7	15:59012307	TACAGGCGTGAGCCA[C/T]TGCACCTGGCCTGCT	54778
rs115379934	snp	C/T	0.000997506	0.0223105	intron-variant, utr-variant-5-prime	RNF111	GRCh38.p7	15:59004089	TTGAAACCCTCTTCC[C/T]AGACTCTTGGATTTA	54778
rs115389010	snp	A/G	0.00636936	0.0560724	intron-variant	RNF111	GRCh38.p7	15:59084307	GCTTGTGGTAAAACT[A/G]TTGGAAGAGATGCCT	54778
rs115407968	snp	A/G/T	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:59078200	AATTGTGATACTTGG[A/G/T]TCCAGATGAATAGTT	54778
rs115447366	snp	A/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:58997419	GATGGTGCAAAAAAC[A/T]GTGGTGCATTAAACT	54778
rs115498689	snp	A/G	0.127599	0.217986	intron-variant	RNF111	GRCh38.p7	15:59044180	GGATTAGAGGCACAC[A/G]TCACCATGCCCAGCT	54778
rs115519628	snp	A/G	0.00636936	0.0560724	intron-variant	RNF111	GRCh38.p7	15:59083978	TTAACAAATAATTTT[A/G]TATGTTTTTATAATT	54778
rs115636176	snp	A/C	0.021333	0.101051	intron-variant	RNF111	GRCh38.p7	15:59039558	TTTTTAAATGATTTC[A/C]TCTTTGGCCATTGGG	54778
rs115696726	snp	A/T	0.00636936	0.0560724	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096195	TTGGAGGAAGTTTTA[A/T]TCTACTTCAGGATGC	54778
rs115700889	snp	G/T	0.0333238	0.124705	intron-variant	RNF111	GRCh38.p7	15:58991248	GTTCCACTGAGCTGA[G/T]ATCTGCACTCCAGCC	54778
rs115711400	snp	A/G	0.0494327	0.149241	intron-variant	RNF111	GRCh38.p7	15:59008859	GTCTTTCTTCAAGGA[A/G]TAATAGACGGTTGTA	54778
rs115749091	snp	A/G	0.0279526	0.114869	intron-variant	RNF111	GRCh38.p7	15:59062452	CTGTCTGACCTCTCC[A/G]TGTGGTCCTTGTGTT	54778
rs115809334	snp	A/G	0.0402882	0.136092	intron-variant	RNF111	GRCh38.p7	15:59044016	AGTTTGTGCTCACAG[A/G]TTGGAAACTGTCTTT	54778
rs115864886	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59082393	AGATCTAAAGATATC[A/G]AAGATTTGAATGTTA	54778
rs115878416	snp	A/G	0.0103295	0.0711199	intron-variant	RNF111	GRCh38.p7	15:58988565	GTCATTTAAAAAGAA[A/G]CTGATGTTTTTACTA	54778
rs115879211	snp	A/G	0.0399052	0.1355	intron-variant	RNF111	GRCh38.p7	15:59018171	TATTATCATTTTCGA[A/G]CATTAAAATTTATTT	54778
rs115995534	snp	C/T	0.0372196	0.131242	intron-variant	RNF111	GRCh38.p7	15:59037558	ATTAATAGGTATTGC[C/T]GGGCGTGGTGGCTCA	54778
rs116092126	snp	C/G	0.046775	0.145601	intron-variant	RNF111	GRCh38.p7	15:59070087	GCCTTGTTTCTCAGG[C/G]TGGCCTTAAACTCCT	54778
rs116095414	snp	A/T	0.0240643	0.107019	intron-variant	RNF111	GRCh38.p7	15:59074239	GCATTGGATTTTAAG[A/T]CACTAGCTACATTAG	54778
rs116203990	snp	C/T	0.00557542	0.0525036	intron-variant	RNF111	GRCh38.p7	15:58991356	TTTTAAAGAGCGGTA[C/T]TGCATTATTACGTAG	54778
rs116286018	snp	A/G	0.0368353	0.130617	intron-variant	RNF111	GRCh38.p7	15:58994956	TTTTCCAGTTTTGTC[A/G]AATTGTCCTGATAAT	54778
rs116294657	snp	C/T	0.00874735	0.0655527	intron-variant	RNF111	GRCh38.p7	15:59002853	TTTCCTATTTTTTCT[C/T]TCCCAGGAATACTCT	54778
rs116343303	snp	C/T	0.0368353	0.130617	intron-variant	RNF111	GRCh38.p7	15:59047657	CTTGGCTCACTGCAA[C/T]GTGCGTCTCCCAGGC	54778
rs116347199	snp	C/G/T	0.00478085	0.0486577	intron-variant	RNF111	GRCh38.p7	15:59087633	AATACATTTACTATT[C/G/T]GTTAAGTGAAAGTGT	54778
rs116376298	snp	C/T	0.0414363	0.137845	intron-variant	RNF111	GRCh38.p7	15:59005499	TCTCAGGACAGCTGT[C/T]ATCTTTTTAATTTAG	54778
rs116397501	snp	C/T	0.00716266	0.059414	intron-variant	RNF111	GRCh38.p7	15:59024692	GGTCGTTTAAATGTA[C/T]GTAACATAAAATTAC	54778
rs116398850	snp	A/G	0.00835141	0.0640778	intron-variant	RNF111	GRCh38.p7	15:59033773	AATACTTACTGTAGC[A/G]TGTGTGTTTTTTTTC	54778
rs116399225	snp	A/G	0.00755907	0.0610114	intron-variant	RNF111	GRCh38.p7	15:59076798	TGTAACATATTTACT[A/G]TTTTGTTAGATCATA	54778
rs116402019	snp	A/C	0.0611083	0.163768	intron-variant	RNF111	GRCh38.p7	15:59082733	ATTTCCCGTTTTACC[A/C]TTCACATAACCTGTT	54778
rs116431118	snp	C/G	0.0329836	0.124112	intron-variant	RNF111	GRCh38.p7	15:58991195	ATCCTGGCTGCTCAA[C/G]AGGGTAAGGCAGAAT	54778
rs116515818	snp	C/T	0.0494327	0.149241	intron-variant	RNF111	GRCh38.p7	15:59059553	GGGAGTTTTTAAAAT[C/T]TTGGTGATATCCATT	54778
rs116541195	snp	A/C	0.0490535	0.14873	intron-variant	RNF111	GRCh38.p7	15:59013167	CAGGGGAAGTTTGTA[A/C]ATAATACCCTTGTTT	54778
rs116564318	snp	C/T	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:59086022	GTGGGGTTTTTTGTA[C/T]ACCAAGATACTCTTA	54778
rs116569445	snp	A/G	0.0166325	0.0896639	intron-variant	RNF111	GRCh38.p7	15:59037191	GCTTCTTGCTGTCCC[A/G]TTATTAATTGGCTTT	54778
rs116626775	snp	C/T	0.0437281	0.141251	intron-variant	RNF111	GRCh38.p7	15:59076688	AACATAGTGAGACCC[C/T]GTTTCTATAAAAATA	54778
rs116634158	snp	A/C	0.0513262	0.151752	intron-variant	RNF111	GRCh38.p7	15:59015578	GTTAAACAGAAACCT[A/C]TAATCCCTCACTCTG	54778
rs116680294	snp	A/T	0.00874735	0.0655527	intron-variant	RNF111	GRCh38.p7	15:59063755	GAACAGATACATGTC[A/T]TATCCATCACTTTAG	54778
rs116689934	snp	C/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59057611	ATAAGTTGAAGTCTA[C/T]CTGAAATTTCTTTTA	54778
rs116750621	snp	C/G	0.0185938	0.0946107	upstream-variant-2KB	RNF111	GRCh38.p7	15:58987549	GGGGAGGGCCGGGAC[C/G]GAGGGGGCGGGACGG	54778
rs116763896	snp	A/G	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:59071008	TGTATTCAAGAATAC[A/G]AAGAAGTGGCCGGGC	54778
rs116806597	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59028795	AATTTTTTTTTTTTT[C/T]TTGAGATAGAGTCTT	54778
rs116968583	snp	C/G	0.0460142	0.144533	intron-variant	RNF111	GRCh38.p7	15:59013913	TATGCCTCAGCGTCC[C/G]GAGTAGCTGGGGTTA	54778
rs116971019	snp	A/G	0.0372196	0.131242	intron-variant	RNF111	GRCh38.p7	15:58990990	GAGTGAATTACAAAT[A/G]TTTAAAGACAAATAC	54778
rs117036951	snp	C/T	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:59037129	GTGTGAGCCACTGCA[C/T]GTAACCAGTGTATTT	54778
rs117045805	snp	G/T	0.0162398	0.0886349	intron-variant	RNF111	GRCh38.p7	15:59080798	GTTGCTTGAGCAGTT[G/T]CTTGAATACTTTACT	54778
rs117125233	snp	A/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59091312	AAAAAATATATACTT[A/T]GCAGTTTTTTACTCT	54778
rs117165372	snp	C/T	0.0119091	0.0762411	intron-variant	RNF111	GRCh38.p7	15:58990145	TATACATTAGATCTC[C/T]GAGTTTATTGTTAAC	54778
rs117199636	snp	C/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59062422	AAACTCAATGTGCCA[C/G]AAACAGCTCATTATC	54778
rs117222149	snp	C/G	0.0360663	0.129354	intron-variant	RNF111	GRCh38.p7	15:59018377	TAAGAAATTTTATGC[C/G]TAGCCAAGATTCCTG	54778
rs117256818	snp	A/G	0.0142736	0.0832652	intron-variant	RNF111	GRCh38.p7	15:59045540	AAATTTTGTATACAG[A/G]TAAATGGAGAAAAAT	54778
rs117259272	snp	C/T	0.00478085	0.0486577	intron-variant	RNF111	GRCh38.p7	15:59072117	AGCAATCCTCTGAGA[C/T]TTCAGCAAATTGTAA	54778
rs117267878	snp	G/T	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59070707	TCTTTCCCAACTTGA[G/T]TATCATCACACCCCT	54778
rs117313815	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020303	TATATATTGTAATAT[A/G]TAGTAATTAATTAGC	54778
rs117329856	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59053758	TTTTTCCTTGTAGGA[C/T]TAGAGATCTTGTTTT	54778
rs117373177	snp	G/T	0.0182019	0.0936463	intron-variant	RNF111	GRCh38.p7	15:59062782	CCTAGGCAGTCTGGC[G/T]TGGTACCTCTACTTT	54778
rs117375620	snp	C/T	0.00636936	0.0560724	intron-variant	RNF111	GRCh38.p7	15:59035253	ATTTGGGTAGGGATA[C/T]AGCCAGACCATATCA	54778
rs117415144	snp	C/G	0.0111196	0.0737302	intron-variant	RNF111	GRCh38.p7	15:59004244	CCTTCTTTTCTCTCC[C/G]AATTATCTTTACTGA	54778
rs117478117	snp	C/G	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59015896	AGGTTCTCACGCCCA[C/G]GTTGGAGTGCAGTGG	54778
rs117487204	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:58990250	AATTTAATGGTTTGT[A/G]TATCTAGTTAGGTTT	54778
rs117565956	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59084701	ATGCTGTGCAGTAGA[A/C]TATCAGAACTTACTC	54778
rs117664806	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58990604	GCAGTAAGCGGAGAT[C/T]GTGCCACTCACTGCA	54778
rs117819786	snp	C/G	0.0640965	0.167152	intron-variant	RNF111	GRCh38.p7	15:59016739	CTGGGCCACGGACTG[C/G]TACCCATCTGTGGCC	54778
rs117851759	snp	C/T	0.0360663	0.129354	intron-variant	RNF111	GRCh38.p7	15:59019016	GCAGCCTCTGCCTTC[C/T]GGGCTTGAGTGATCC	54778
rs117878467	snp	C/T	0.0298908	0.118541	intron-variant	RNF111	GRCh38.p7	15:58998346	GATTATTTCACCACC[C/T]AGGTATTAAGCCTAG	54778
rs117893267	snp	C/T	0.00874735	0.0655527	intron-variant	RNF111	GRCh38.p7	15:58990627	TCACTGCACTCCAGC[C/T]TGGGCGACAGAGCGA	54778
rs117919185	snp	C/T	0.0577344	0.159793	intron-variant	RNF111	GRCh38.p7	15:59047854	TGCTGGGATTATAGG[C/T]GTGAGCCACTGTATC	54778
rs117930256	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:58990317	CCAGAAAGAAATGCT[A/G]TACAAAAAGCATCAA	54778
rs117936088	snp	C/G	0.031825	0.122064	intron-variant	RNF111	GRCh38.p7	15:59001802	ACTAAGTACAGTAGT[C/G]CTCCCTTATCCATGA	54778
rs117955606	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59029424	AACTACAGATAGCGC[A/G]TGATGGCTGATCTTG	54778
rs117981647	snp	C/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59089066	CTGGGAACAGAGTTG[C/T]ATGTTGGGCAACTGC	54778
rs117994057	snp	A/C	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59032918	TCTCACACACACAGT[A/C]AATGTGATATTTAAG	54778
rs118060408	snp	A/G	0.0174175	0.0916809	intron-variant	RNF111	GRCh38.p7	15:58993600	TCTTTTCATTTTGAT[A/G]AAAATACAGTATTTC	54778
rs118083049	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59018500	TATGTTCTCATAATT[C/T]ATTTCCTTAAAAAAT	54778
rs118091861	snp	A/G	0.0295035	0.117819	upstream-variant-2KB	RNF111	GRCh38.p7	15:58987299	CTTTATGTCATTAGC[A/G]CATATGATATGGGTA	54778
rs118119186	snp	A/G	0.00438332	0.0466095	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096426	ATAACTTATATTTCT[A/G]TTGTCTTTGTGTTTC	54778
rs118138393	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59056623	TTAGAGGCCATATAC[A/G]ATCAGCTCTTCTATG	54778
rs137875551	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990481	TGGTGAAACCCCATC[G/T]CTACTGAAAATACAA	54778
rs137879390	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59069750	AATTAACCAAATGCT[C/T]ATAAAATAGCTTCAT	54778
rs137891101	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59042413	TTATAGGCGTGAGCC[A/T]CTATGGCTGTCCAAC	54778
rs137923008	snp	A/G	0.000511159	0.0159787	synonymous-codon	RNF111	GRCh38.p7	15:59052405	TGACAGTGAAGTGGA[A/G]ATTGTAACAGTTGGA	54778
rs137950379	snp	A/G	0.00716266	0.059414	intron-variant	RNF111	GRCh38.p7	15:58992335	CAGACGTGGGCCACC[A/G]TGCCCAGCAATGTCT	54778
rs137968526	snp	A/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59078505	GTTATCACACCTGTG[A/G]ACAATCCTTGTACTC	54778
rs137998261	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59025180	GTGAGCCACTGCGCC[C/T]AGGCAGAAATCAAGT	54778
rs138021293	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59019145	TGAGGTTTCATGTTG[C/T]CCAGGGTGGTTTTGA	54778
rs138023730	snp	A/G	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:58993027	ATACAAAAAGTAGCC[A/G]GGCATGGTGGCGGGT	54778
rs138026161	snp	C/T	0.00874735	0.0655527	intron-variant	RNF111	GRCh38.p7	15:59046276	AGGGGTCCCTGCAGC[C/T]TCAGCCTCCAGGGCT	54778
rs138033000	snp	C/T	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:59082069	GGTGACACAGGGAGA[C/T]CCTGTCTCTCCCCCT	54778
rs138085526	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59056570	AATTGGGCAAAGAAT[A/G]TATCAGGTAGATGGA	54778
rs138093957	snp	A/G	0.00438332	0.0466095	intron-variant	RNF111	GRCh38.p7	15:59002046	GAAATGAGGTTAATG[A/G]CATGGGCACTGTGTA	54778
rs138143759	snp	C/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59022763	TAATAGGAAACTTCT[C/T]ATTATTAATATCAGC	54778
rs138156689	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59016897	GCATTCTTGTAGGAG[A/C]ATGAACCCTATTGTG	54778
rs138180133	snp	A/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59030580	GTAGGCTTATGCTCT[A/G]TATCTACTGTATTTC	54778
rs138227222	snp	A/G	0.00597247	0.0543191	intron-variant	RNF111	GRCh38.p7	15:59025822	CGCAACCGCTGCCTT[A/G]CGGATTCAAGCGATT	54778
rs138233569	snp	G/T	1.66363e-05	0.00288407	intron-variant	RNF111	GRCh38.p7	15:59091163	CAAAAAGGTAAGAAT[G/T]TATTCTATGAAACTT	54778
rs138264576	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59073254	CTGAGGCAGGCAGAT[C/G]ACTTGCGGTCAGCAG	54778
rs138296332	snp	A/T	0.0325976	0.123435	intron-variant	RNF111	GRCh38.p7	15:59034715	CATATTTTGAGTGAT[A/T]CAAATAAAATGATTT	54778
rs138348721	snp	A/G	0.0111196	0.0737302	intron-variant	RNF111	GRCh38.p7	15:59061258	CCTCTCTTAAGGTCA[A/G]TTTCCTTCCAGGACC	54778
rs138367923	snp	A/G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59016477	ATTGTGAGCTTCTTG[A/G/T]AGGATGGGAACCTGT	54778
rs138399319	snp	A/C	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59012540	CTGAACATTTTAACA[A/C]AAGAAATGTGTTTAT	54778
rs138401147	snp	C/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59005985	TTTGAGTTGCCTGAG[C/G]AAAGAATTCCAAAAT	54778
rs138410657	snp	C/T	0.0146672	0.084371	intron-variant	RNF111	GRCh38.p7	15:59064093	TAATGTTGGGTTCAG[C/T]ATAGCCCTAAAAGAC	54778
rs138414973	snp	C/T	4.95798e-05	0.0049787	synonymous-codon	RNF111	GRCh38.p7	15:59031617	CCTCAGCAGTGAATC[C/T]TCTTCTAGCTCATCA	54778
rs138453929	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59039112	TGGGATTACAGGCAC[A/G]TGCCACCATACCTGG	54778
rs138485815	in-del	-/ATCTC	0.0513262	0.151752	intron-variant	RNF111	GRCh38.p7	15:59059680	TTAGTTTTAGCTCTT[-/ATCTC]AAGCTAGTTCTTACG	54778
rs138488275	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59008637	TGTCCTTACACCAAT[A/G]GCCCCAGTGTTGATA	54778
rs138488340	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59041819	GGGGGTTTTTGGTCC[A/G]TCTGATAGCTGAGAA	54778
rs138508204	snp	A/G	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:59003296	TTTTTGTAGAGACAT[A/G]CTTTTGCCCTGTGGC	54778
rs138647504	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59000460	CTCACATCTGTAATT[A/G]CAGCACTTTGGGAGG	54778
rs138650199	snp	C/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59027899	GGTGTGATCTCAGCT[C/T]ACTACAACCTCTGCC	54778
rs138658453	snp	C/T	0.00256165	0.0356968	synonymous-codon	RNF111	GRCh38.p7	15:59055715	ACACTCCAGATCTCA[C/T]TGGAGCCAGGGTTCC	54778
rs138659988	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59051145	ATGATTTAGAAAAGA[A/G]CGGGCATTTAAAAAT	54778
rs138690293	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59018561	TTTTAGAAAAAAAAC[A/C]AACTATATATACAGA	54778
rs138695477	snp	A/G	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59043056	TGTATCTTGCAGAGA[A/G]CGTTTTATGTTCTTT	54778
rs138698339	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59085422	CTTCCTTTGTAAGAT[A/G]TGAAACCAAGTAGAA	54778
rs138732174	snp	C/T	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:59090370	GAGTAGCTGGGATTA[C/T]AGGTGCCCGCCACCA	54778
rs138737362	snp	C/T	0.0107246	0.0724382	intron-variant	RNF111	GRCh38.p7	15:59045677	TTGATACATAATGCT[C/T]TTAGTTTTAAATGTA	54778
rs138756371	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59068465	ACAAAAATTAGCTGG[C/G]TGTGATGGTGTGTGC	54778
rs138764503	snp	A/G	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:58997488	GCATTAGTAATCACT[A/G]TGTTCTTCATGACTA	54778
rs138766434	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	RNF111	GRCh38.p7	15:59095875	ACTGGCAGGTATCTG[G/T]GCATTCATAGAACTT	54778
rs138811205	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59086751	TAAGCTGGTGTTTCT[A/C]ATTTTAGGAGTGAGG	54778
rs138822419	snp	C/T	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59082369	TAAAATTGATGATTC[C/T]GAGGAATAAGATCTA	54778
rs138823657	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59056923	TTCCACATTACAGTA[A/G]GTTCAACCAGAATTT	54778
rs138877485	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990733	TAGATATTAATTACT[A/G]AAGCTTTAATAGCTT	54778
rs138912549	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59007915	ATACACACACAAACA[C/G]ATGTATATATAATTT	54778
rs138945924	snp	C/T	0.0456336	0.143994	intron-variant	RNF111	GRCh38.p7	15:59039041	ACGATCTCAGCTCAC[C/T]GCAACCTCTGCCTCC	54778
rs139013961	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59002873	AGGAATACTCTTCCT[C/T]TAGAATTGTGTGGCT	54778
rs139023903	snp	C/T	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59035049	AAGGTGAATGAAGAG[C/T]AAAGTCACGTCTTAC	54778
rs139024825	snp	A/T	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59077618	TAGCTCATTGGTTTT[A/T]AATACCCCCATAATA	54778
rs139093709	snp	A/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59028425	GATAAAGTTTAATTT[A/T]TAAATTAGGCAGAAT	54778
rs139104742	snp	C/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59006899	TCAAGCAGTTCTCTG[C/T]CTCAGCCCCCCGAGT	54778
rs139105210	snp	C/T	1.64852e-05	0.00287094	missense	RNF111	GRCh38.p7	15:59030959	AGCCCATTGGGGCAG[C/T]CAAAAGTTTTCCTGC	54778
rs139160355	snp	A/G	0.0011034	0.0234623	missense	RNF111	GRCh38.p7	15:59031303	GATGAGGATAAAGAA[A/G]TCTCTGTAAGACATT	54778
rs139165449	snp	A/G	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59062414	GTCAGTTCAAACTCA[A/G]TGTGCCACAAACAGC	54778
rs139175210	snp	A/G	0.00279162	0.0372561	utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58987954	ATTAGGCCGACGTCT[A/G]AGGCGCAGATCGCTG	54778
rs139177306	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59040458	TGTTTTAACAGACAA[A/G]GCTAGAAATGTAAAG	54778
rs139227387	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59066343	AGCCGGGGTGTGGTG[A/G]CTCACGCCTGTAATC	54778
rs139253302	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59079027	TCTAGGAAACAATAT[C/T]AAGAACTTTTTTTAA	54778
rs139290644	in-del	-/A/AAA/AAC	0.129712	0.221489	intron-variant	RNF111	GRCh38.p7	15:59081531	AACAGCAACAACAAC[-/A/AAA/AAC]AAAAAAAACCATGAA	54778
rs139318473	in-del	-/GGTT			frameshift-variant	RNF111	GRCh38.p7	15:59076009	TCATGGAAGTGGCAG[-/GGTT]TTTTCATGGAGCATC	54778
rs139352097	snp	A/G	0.00716266	0.059414	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021242	TGCAAACTCCGCCTC[A/G]TGAGTTCAAGTGATT	54778
rs139359759	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59083615	ATGTGTTTTGAAAAA[A/G]AATGCACAGGGTTAA	54778
rs139363948	snp	A/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020271	CAATATATGCATTAT[A/T]TATAGTAAATATGCA	54778
rs139390682	snp	C/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59065286	AGTTTCCATATAATA[C/T]TTAGTTTGAGGAAGC	54778
rs139422991	snp	C/G	0.00557542	0.0525036	intron-variant	RNF111	GRCh38.p7	15:59028893	CAAGCGATTCTCATG[C/G]TTCAGCCTCCCAAGT	54778
rs139491637	snp	C/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59010139	TGGAATACATGTTAT[C/T]GGCAAATTTTTAATT	54778
rs139494565	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59069905	ATAAAAATTAGACTG[A/G]CATACCGAGAAGATG	54778
rs139508391	snp	C/T	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:59052916	TGTTTTATAAAATTG[C/T]GTTTTTTAATGATAT	54778
rs139510078	snp	A/C	0.00795532	0.062565	intron-variant	RNF111	GRCh38.p7	15:59017335	ATAAGAGAAACACCA[A/C]GCCATTTAATAGCAT	54778
rs139591059	in-del	-/AG	0.0372196	0.131242	intron-variant	RNF111	GRCh38.p7	15:58990881	ACATTTGAATGTCTT[-/AG]ATACCTCTGTTTGTT	54778
rs139640186	snp	C/T	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59046936	ACAATGGCACAGTCT[C/T]GGCTCACTGCAGACT	54778
rs139647295	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59014069	ATGCTAGGATTACAG[A/G]TGTGAGCCACTGCCG	54778
rs139679728	snp	A/G	4.99222e-05	0.00499586	missense	RNF111	GRCh38.p7	15:59055768	AGGAGCCACGGAACC[A/G]CAGTAGGATTTCTAC	54778
rs139687390	snp	A/G	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59044132	ACCTCCCGGGTTCAA[A/G]CGATTCTCCTGCCTC	54778
rs139742512	snp	C/G	1.64738e-05	0.00286995	missense	RNF111	GRCh38.p7	15:59076098	GCCGCTGCTGCTGCC[C/G]CAAGTCAACCTTTAT	54778
rs139743964	in-del	-/A	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:58988956	TTTATTTCATTTGGT[-/A]TTTTATCTATAATTT	54778
rs139770103	in-del	-/TA	0.0737376	0.17729	intron-variant	RNF111	GRCh38.p7	15:59086052	ATCCACTGTCAGGAG[-/TA]TATACTGTGCTTCAG	54778
rs139780739	in-del	-/GAG	0.0310518	0.120672	intron-variant	RNF111	GRCh38.p7	15:59001235	GGAGTAGGTGAGGAG[-/GAG]AATGGTGGTCTCTGA	54778
rs139787218	snp	A/T	0.00636936	0.0560724	intron-variant	RNF111	GRCh38.p7	15:59011041	TTTGGCATCTTGAAG[A/T]TGAAAAATTGTCTAT	54778
rs139804208	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59004246	TTCTTTTCTCTCCCA[A/G]TTATCTTTACTGATC	54778
rs139823953	snp	A/G	1.64874e-05	0.00287113	synonymous-codon	RNF111	GRCh38.p7	15:59076175	CCAGCCCCCTCCACA[A/G]CCCTCTCTCTCATCA	54778
rs139836815	snp	A/G	0.00755907	0.0610114	intron-variant	RNF111	GRCh38.p7	15:59006703	ACAAAAATAAAAAAA[A/G]TAAAGTTACAGACGC	54778
rs139850173	snp	C/G	0.0150606	0.0854603	utr-variant-3-prime	RNF111	GRCh38.p7	15:59097372	GCTGCTAGCACACTT[C/G]AGCATTTGAACCATA	54778
rs139877473	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59032662	CTTAGCTCAGGCGAT[C/G]CACCTGCCTTGGGCT	54778
rs139882098	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59048901	TTCGAGACCAGCCTG[A/G]GCAGTGTACTAAGAT	54778
rs139925971	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59045469	GCTGGGATTACAGGC[A/G]TGAGACACTGCGCCC	54778
rs139999361	snp	C/G	0.0150606	0.0854603	intron-variant	RNF111	GRCh38.p7	15:59003601	GAGACAGGGTTTTGC[C/G]GTGTTGCCCAGGCTG	54778
rs140015365	snp	C/T	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:58991367	GGTACTGCATTATTA[C/T]GTAGATACATTTATT	54778
rs140019770	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59087673	AAGGTCTCTTTCCTT[A/G]TTGTCTTCACATTGA	54778
rs140030885	snp	A/G	3.29701e-05	0.00406005	missense	RNF111	GRCh38.p7	15:59031355	AAAGTAGAAGCCATA[A/G]TGCACGGTCTCATAA	54778
rs140037835	in-del	-/CAGCCTCTAGAA	0.14933	0.228835	intron-variant	RNF111	GRCh38.p7	15:59005314	ACGAGCCACTGCACC[-/CAGCCTCTAGAA]CATAGGCTTTCATTA	54778
rs140059029	snp	C/T	0.000346168	0.0131516	intron-variant	RNF111	GRCh38.p7	15:59081328	CAAGTTTGCTTTTTC[C/T]TCTACTTCCATTGGT	54778
rs140067516	snp	A/C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59001274	AGGTATGAAGGGTTC[A/C/T]TGTTCTTCAGTTATA	54778
rs140072751	snp	A/G	0.00716266	0.059414	intron-variant	RNF111	GRCh38.p7	15:59058138	TGGAATAAGCATATC[A/G]GTGTTGGATTTTTTT	54778
rs140087695	snp	A/G	0.0581099	0.160244	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020976	TGGTTACATGAATAA[A/G]TTCTTTAGTGGTGAT	54778
rs140100939	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59081975	GGCTGGAGTGCAGTG[A/G]TGCAACCATAGTTCT	54778
rs140157028	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59093427	CTCAGCTCACTGCAA[C/T]CTCCACCTCCTGGGC	54778
rs140214024	snp	A/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:58999129	CCTTTTTCAACTACA[A/T]ATTTGTGTGAAACTG	54778
rs140218660	snp	C/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59053967	TTGAGACAGAGTCTC[C/T]CTCTGTCACCCAGGC	54778
rs140221840	snp	C/G	0.00597247	0.0543191	intron-variant	RNF111	GRCh38.p7	15:59026918	CACCAAACCACCCCC[C/G]CTTGCTCTCCTCTAC	54778
rs140230887	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59093720	GAAACAGGTTCTATA[C/T]CATATATAACAGAAC	54778
rs140267327	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59004461	AAGGGTAGCACCTTA[C/T]TATCTTTTTATCACC	54778
rs140335253	snp	A/C	0.0444908	0.142359	intron-variant	RNF111	GRCh38.p7	15:59001967	ATAAAAATTGTGTGA[A/C]TGTCATCTCTCAAAA	54778
rs140344199	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59059864	TGGATTGACTAAATC[A/C]CCATTAATAATGAAA	54778
rs140365796	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59067826	ACTGTAGAGTTCACT[A/G]TAACCTTCACTCATC	54778
rs140381669	snp	A/G	0.00597247	0.0543191	intron-variant	RNF111	GRCh38.p7	15:59094500	CTCCAGGGCATTGGC[A/G]GCTCCTGTACCAAAA	54778
rs140407630	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59030052	AATGCTTTAAATTCA[A/G]ATCTCTTTTTGGCAG	54778
rs140420056	snp	G/T	0.000413712	0.0143765	missense	RNF111	GRCh38.p7	15:59066790	AGAACTACATCTAGT[G/T]CTGTAACGGAAACTG	54778
rs140444564	snp	C/G/T	0.00119737	0.0244387	downstream-variant-500B	RNF111	GRCh38.p7	15:59097570	TTTGAACCATAACAG[C/G/T]TGACTTAGAGAAAAC	54778
rs140450434	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59056137	TTTGTAATAATGATT[G/T]TCTTTAACTTGCCAT	54778
rs140473663	snp	A/G	0.00874735	0.0655527	intron-variant	RNF111	GRCh38.p7	15:58991717	GATTCTAGAGAATCT[A/G]CAAATGTAAATTAAT	54778
rs140481464	snp	A/G	0.0119091	0.0762411	intron-variant	RNF111	GRCh38.p7	15:59011936	GATTGTCAAAGTTGG[A/G]ACCAAAGATTCCTAG	54778
rs140481963	snp	C/T	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:59072653	GAGACGGGGTTTCAC[C/T]GTGATAGCCACGTTG	54778
rs140491514	snp	C/T	0.0103295	0.0711199	upstream-variant-2KB	RNF111	GRCh38.p7	15:58987357	TGATGTTTTTGTTTA[C/T]GTATATCTGTAAATG	54778
rs140499450	snp	C/T	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59039966	ATGATCCACCTGCCT[C/T]AGCCTCCTCAAGTGC	54778
rs140572228	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59075628	AGTATGATTTTTAAA[A/G]TTTCTAAGATGTATT	54778
rs140585316	snp	A/C	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59016414	ACTTCGTGATCTGCC[A/C]ACTTTGGCCTAATTA	54778
rs140626292	snp	C/T	0.0448719	0.142907	intron-variant	RNF111	GRCh38.p7	15:59014865	GGCTCAAGCGATTCT[C/T]CTACCTCAGCCTTCT	54778
rs140640294	snp	A/C	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59037304	AGTTTTTCCCAGTTG[A/C]CAGTGAGGCTGATAA	54778
rs140666244	snp	C/T	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:59041425	CGGGTGTGGTGGCTG[C/T]ACCTGTAATCCCAGC	54778
rs140702737	snp	G/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59077811	CACACCTCATTAGGA[G/T]TGTGTTAATGAGAAT	54778
rs140735665	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59039042	CGATCTCAGCTCACC[A/G]CAACCTCTGCCTCCC	54778
rs140795840	snp	C/G	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:59059632	AAACCGTTGCCTAAT[C/G]CAGGGTCACAAAAAT	54778
rs140836718	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59001134	GCCTCGTGGTTATCT[A/G]GGGGAAGAGCATTCA	54778
rs140862171	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59029448	GATCTTGGATACAGC[A/G]CTGCCTGTGCTTGTG	54778
rs140862211	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59000133	ATATAATAAAAGCTT[C/T]TTCAGATCTTCCAGT	54778
rs140900053	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59004838	AGTAGGTTTGTGTAT[A/G]TGGCCTATAATATGG	54778
rs140900368	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59063229	TGCAAGCATGTTTCT[A/G]GTTGCTAGAGATAAA	54778
rs140913535	snp	C/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59026230	TCCTCCTTTTGCTCA[C/T]ATAAACTTGTTTATG	54778
rs140925536	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59001680	AAATACTTAATACTT[C/T]TATTAAGTGAAGAAA	54778
rs140947433	snp	G/T	0.000197945	0.00994651	missense	RNF111	GRCh38.p7	15:59031393	CGGACTGAGACAGAA[G/T]CTGTATCGGGATTGT	54778
rs140971346	snp	C/G	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59038260	CACTAGAAACTTTGT[C/G]TCAAACTACAAATAT	54778
rs140988886	snp	A/C	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59058950	CTTTATCTGATAAGC[A/C]CTTTAGAATCCAGAA	54778
rs141005553	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59007800	TTATTGGGTATTTTT[A/G]TATGTTTTGTAAAAT	54778
rs141019186	snp	A/G	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59094182	AGCACAATATTAAGT[A/G]TATATAACAATTATT	54778
rs141040018	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58995132	GCTACTCTGCTCCTC[A/G]TCAGATCATCCTGTT	54778
rs141050053	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59061663	CTTTCCCTTCCAGTT[C/G]CTTTATCTGTGCTCT	54778
rs141050134	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59023909	GGACATGAAGAGTGA[C/T]CTTAATAGACTTTCT	54778
rs141074666	snp	C/G/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:58990424	CAGCACTTTGGGAGG[C/G/T]CAAGGCGGGCGAATC	54778
rs141083598	snp	C/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59042014	TACTGGTCTTCATTC[C/T]TCTATCCATTTTTAG	54778
rs141194792	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59074118	TTCAGTAAACCACGT[A/G]AATAGCTGTACTGTC	54778
rs141229852	snp	A/G	0.00557542	0.0525036	intron-variant	RNF111	GRCh38.p7	15:59035912	TTTGGAGCTCTCCAA[A/G]CTTTTGCAACCTCTG	54778
rs141261732	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59022700	TAAATCATTCTTCCA[A/G]TGTCTTTTAAATGCA	54778
rs141263191	snp	C/T	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59050184	ATTTTCCTGCCTCAG[C/T]CTCCTGAGTAGCTGG	54778
rs141310339	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58988963	CATTTGGTATTTTAT[A/C]TATAATTTTCTTGTT	54778
rs141349598	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59015672	CCCAAGCATTAGAGT[A/G]TTTAGATGTTGCCAT	54778
rs141352550	snp	C/T	0.00755907	0.0610114	intron-variant	RNF111	GRCh38.p7	15:59076593	GGTTGGGCATGATGG[C/T]TCACTCCTGTAATCC	54778
rs141362511	snp	A/C	9.88338e-05	0.00702902	missense	RNF111	GRCh38.p7	15:59066880	TCGTCACAGAACCAC[A/C]ATGCATTAGGACATC	54778
rs141393458	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59007499	TTTTCTCTAATTTTT[A/G]GCTATTATGAGTAAA	54778
rs141414694	snp	A/G	0.00118708	0.0243337	missense	RNF111	GRCh38.p7	15:59091090	AAGAAAGATTAGGCA[A/G]TGTCAATCGTGGAGC	54778
rs141471543	snp	C/T	0.00597247	0.0543191	intron-variant	RNF111	GRCh38.p7	15:59073260	CAGGCAGATCACTTG[C/T]GGTCAGCAGTTCAAG	54778
rs141537519	snp	A/G	0.0333695	0.124785	intron-variant	RNF111	GRCh38.p7	15:59037763	ATGGCTTGAACCTGG[A/G]AAGCAGAGGTTGCTG	54778
rs141550706	snp	A/G	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59065888	TGGTGGTGTGTGCCT[A/G]TGGTCCCAGCTACTT	54778
rs141592141	in-del	-/CT			intron-variant	RNF111	GRCh38.p7	15:59032890	GCTCATGCGTGCTGA[-/CT]CTCTCTCTCTCTCTC	54778
rs141594132	snp	A/G	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59006547	AAAGATGAAAGAATT[A/G]TACAGTGAACGCCCA	54778
rs141602219	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59065197	AGGATGGCAGCAGGG[C/T]GGGGCTTTGGCTTTA	54778
rs141630373	snp	A/G	8.92785e-05	0.00668067	synonymous-codon	RNF111	GRCh38.p7	15:59030831	GTTTCCCATGTCTCA[A/G]TGGACTCCTGAATAT	54778
rs141643472	in-del	-/GGTGATTCATTCAGCAAAGTT			intron-variant	RNF111	GRCh38.p7	15:59055507	ACATAGTATTTCTTA[-/GGTGATTCATTCAGCAAAGTT]TATTCTTAGGTCAAT	54778
rs141645921	snp	C/G	0.000153988	0.00877327	missense	RNF111	GRCh38.p7	15:59055708	CCCTTGGACACTCCA[C/G]ATCTCATTGGAGCCA	54778
rs141672186	snp	G/T	0.0248432	0.108648	intron-variant	RNF111	GRCh38.p7	15:59039829	TCAAGCGATTCCCCT[G/T]CCTCAGCCTCCTGAG	54778
rs141684331	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59034412	CTCGATGCTAATGTC[A/G]TGATGATAATAAAAA	54778
rs141705081	snp	A/G	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59009440	TGGTGATGACTTAAT[A/G]TCAAAGTCAGTATGA	54778
rs141739987	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59050421	ATGGTGGTTTCTGGC[A/G]AAAGGCCAGATTAAA	54778
rs141811026	snp	A/G	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:58997543	AAAAATCAGGGCTGG[A/G]TATGGTGTCTCACGC	54778
rs141819854	snp	A/C	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59049790	TCTCGCTCCGTCACC[A/C]AGGCTGGAGTGCAAT	54778
rs141842662	snp	C/T	0.00438332	0.0466095	intron-variant	RNF111	GRCh38.p7	15:59000617	CGGGAGGCTGAGGCA[C/T]GAGAATTGCTTGAAC	54778
rs141846501	snp	A/C	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:59056729	TGCATTTCATTCAAC[A/C]ATCTCTTGGTTTTTG	54778
rs141848833	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59083074	GGATCACTTAAGCCC[A/G]GGAGTTCAGGGTTAC	54778
rs141878770	snp	A/G	0.103794	0.20279	intron-variant	RNF111	GRCh38.p7	15:59000475	GCAGCACTTTGGGAG[A/G]CCGAGGCAGGCGGAT	54778
rs141908818	snp	A/G	0.00557542	0.0525036	intron-variant	RNF111	GRCh38.p7	15:59086957	CATTATAGTAGAAGA[A/G]GTAAATATTGATGAA	54778
rs141914801	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	RNF111	GRCh38.p7	15:59095268	ACATAGTACCAAGCC[G/T]TGATAATTATGAATT	54778
rs141959456	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:58992628	TTTGAGACTAGGCTG[A/G]GCAATGTGACGAAAT	54778
rs141965735	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59088422	ATGATCTTGGTTATA[A/G]GAAAAGTTGTAAACA	54778
rs141970999	snp	A/G	0.00953873	0.0683987	intron-variant	RNF111	GRCh38.p7	15:59090526	CAAGCCACCGCACCC[A/G]GCCCCCGTTGTGTTT	54778
rs141972852	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59046594	AAGTAGATCATAGAC[A/C]TAAATGTAAGAACTA	54778
rs142028484	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59032052	CAAGCAATTCTCCTG[C/T]GTCAGCCTCCCAAGT	54778
rs142037653	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59062338	GTGAGCCACCATGCC[C/T]GGCCATTTTAGACTT	54778
rs142070424	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59026553	AGCCAATAATTTTTA[C/T]AAAAATAAAAGACTA	54778
rs142110775	snp	A/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59085179	GACTTAGCATATAAC[A/T]GTTTTACCCCTTCTA	54778
rs142141117	snp	A/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59066525	TGAGGGAGGAAAATC[A/G]CTTGAACCCAGGAGG	54778
rs142209417	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59017227	TGGAAACCGCTGCTG[C/T]GTAGGCCACGATAAT	54778
rs142217092	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59035111	GGAACTCCCATTTAT[A/C]AAACCATCAGACCTT	54778
rs142239604	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59033616	GAGACAGGATGGTTG[A/G]TGTGGAGCAGAAGTT	54778
rs142243165	snp	C/T	0.00993419	0.0697739	upstream-variant-2KB	RNF111	GRCh38.p7	15:58987376	TATCTGTAAATGTAT[C/T]AATTCTGTAGTTGGT	54778
rs142246039	snp	A/G	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59007449	TCCCGTTGTAGCTGT[A/G]TAACATAATTTATCC	54778
rs142293140	snp	A/T	0.00399502	0.0445146	missense	RNF111	GRCh38.p7	15:59058487	ACCAGTAGCCAACCT[A/T]CCACAGTGTCAGAGA	54778
rs142320227	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021115	CATTCTTATGCCTCT[C/G]TGTCCTCATAGGTTA	54778
rs142343187	snp	C/G	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59071780	TTTCCCAACTTAGTT[C/G]ATGGGCTTTCCCTAA	54778
rs142344212	snp	G/T	0.00111431	0.0235778	utr-variant-5-prime, missense	RNF111	GRCh38.p7	15:59030819	GCTTTCCTTAAAGTT[G/T]CCCATGTCTCAATGG	54778
rs142360398	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59032289	TTATGTATGTTCTTC[A/T]TTTATGGTACACATT	54778
rs142362410	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59073667	TGAACCCCTCAAAGT[A/G]TGCATGAGGCTTGGA	54778
rs142410896	snp	G/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59053674	CCTATCCTCTGACCG[G/T]GCATAGTGCTTGGTA	54778
rs142478514	snp	C/G	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59068389	AGGCAAGTGGATCAC[C/G]TGAGGTCAGAAGTTC	54778
rs142488594	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096919	AGCACAGGTGGATTT[C/T]TCTATTTTTGAATAC	54778
rs142505997	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59069759	AATGCTCATAAAATA[C/G]CTTCATATAGTCTTC	54778
rs142522564	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59059163	AAACAAAAAGCCCCA[A/G/T]CCCAACAGAAAGACA	54778
rs142558829	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58997069	AGTTTTCATGTCAGT[G/T]TAAGTGTCTTTTTTT	54778
rs142592485	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59033207	GTCTTGCCTGTTAAG[A/G]TCAGGGCCTGCTAGT	54778
rs142625026	snp	C/G	0.00874735	0.0655527	intron-variant	RNF111	GRCh38.p7	15:59004686	CAAAAATGGCATTTA[C/G]TCAAAGATAACCTTG	54778
rs142635499	snp	C/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59022979	TGGCTGGGCGCGGTG[C/G]CTTACGCCTGTAATC	54778
rs142662769	snp	C/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:58991142	ACTAAAAAAAAAATA[C/G]AAAAATTAGCTGGGC	54778
rs142666883	snp	C/T	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59043759	AACTTTAATTGTGAC[C/T]GTAAAAGACGAGAGC	54778
rs142678358	snp	A/G/T	0.000115318	0.00759264	missense	RNF111	GRCh38.p7	15:59076086	TTTGGCCATCAGGCC[A/G/T]CTGCTGCTGCCCCAA	54778
rs142695973	snp	C/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59025221	GTTTCATAGCAGTTA[C/T]CGTGAGTATAACTTT	54778
rs142735240	snp	A/G	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:59013866	CTTTCTTGGCTCACT[A/G]CAACCTCTGCCTCCC	54778
rs142735369	snp	G/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59045954	TTGCACTGTTAAAAA[G/T]GCATTTTACCTCAGT	54778
rs142769071	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59016480	GTGAGCTTCTTGAAG[A/G]ATGGGAACCTGTATT	54778
rs142775457	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020506	CTATTGGCTGTAATA[A/G]TAACAGAGTCATTGC	54778

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