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

RNF157

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs754706	snp	C/T	0.38934	0.207568	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154032	AGGTAAATATGGACC[C/T]GTATGTATCTCCTGC	114804
rs754707	snp	C/T	0.443464	0.15834	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154067	CCCGCACCTGACATC[C/T]ATGGCTCTGAGGCCC	114804
rs754708	snp	C/T	0.444666	0.15686	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153888	AGTCCTCCCCCTCCC[C/T]CCAGTGGAAGAAATG	114804
rs881502	snp	C/T	0.444067	0.1576	synonymous-codon, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156285	AGTGAGAATCTCACC[C/T]TGTCGTCATCTGGAG	114804
rs894544	snp	C/T	0.144969	0.226867	intron-variant	RNF157	GRCh38.p7	17:76155375	TCGTGACAGCAAACC[C/T]AAACCTTCTTCAGAA	114804
rs920713	snp	C/G	0.180383	0.240111	intron-variant	RNF157	GRCh38.p7	17:76178804	CCCCCAAGTTTTAGG[C/G]AGCAGAGGTTATTTT	114804
rs1108127	snp	C/T	0.0240643	0.107019	intron-variant	RNF157	GRCh38.p7	17:76204757	AGTACACTGTATGCA[C/T]CTTATTTCTtttctt	114804
rs1376356	snp	C/T	0.305258	0.243817	intron-variant	RNF157	GRCh38.p7	17:76166425	CTTTGGCTGTGCACA[C/T]TGCTCTTTTGTGGCA	114804
rs1465960	snp	C/T	0.401392	0.198948	utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76143183	CCTCAGTCCCATGTC[C/T]AAGGCATACCTAGGT	114804
rs1551104	snp	C/T	0.0154538	0.0865337	intron-variant	RNF157	GRCh38.p7	17:76167284	AATAGAAAAGTTTAA[C/T]GTTGCCAAGCAAGAG	114804
rs1868821	snp	A/G	0.4628	0.13121	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153608	CCACAGAGCAAGGAC[A/G]TAGGAGGAAGAAGGA	114804
rs1868822	snp	A/G	0.442655	0.159323	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153443	AGCAGATGTCATCCT[A/G]TTGCTTCTGCTTTAG	114804
rs1868827	snp	C/T	0.16618	0.23553	intron-variant	RNF157	GRCh38.p7	17:76178936	CCTTGGAAATCTCAT[C/T]TCTAGATTAAAAAGC	114804
rs1947284	snp	G/T	0	0	intron-variant	RNF157	GRCh38.p7	17:76159834	GTGATTTTTTTTCCT[G/T]ACTTTTACTTTTATG	114804
rs2028602	snp	A/G	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76159204	TGGGATAACCTTCAC[A/G]CAAGCAGCTCTGGGA	114804
rs2278824	snp	C/T	0.448708	0.151707	intron-variant	RNF157	GRCh38.p7	17:76167409	ACCCTTTACCTTTTC[C/T]CTTCAAATTGTGCCA	114804
rs2278825	snp	A/G	0.315758	0.241197	intron-variant	RNF157	GRCh38.p7	17:76167397	TTCCCTTCAAATTGT[A/G]CCATCTTGGTATAGT	114804
rs2278826	snp	C/T	0.433963	0.169285	intron-variant	RNF157	GRCh38.p7	17:76166916	AAGGGGCTGCTCGGA[C/T]GCTTGAAGGCCATGC	114804
rs2289602	snp	A/C	2.2677e-05	0.00336719	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76173759	CACCTCCCCAAGAAC[A/C]CGTGAAGACTCTGAG	114804
rs2289603	snp	C/T	0.305829	0.243694	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76167740	AGCTAAAGTCCACTA[C/T]AATGTTGAGTTCACC	114804
rs2289604	snp	C/T	0.126219	0.217206	intron-variant	RNF157	GRCh38.p7	17:76160700	AACCAAAATTAAAAG[C/T]TAGACAACAAATAGT	114804
rs2289605	snp	C/G	0.431029	0.17242	intron-variant	RNF157	GRCh38.p7	17:76160671	GTGTTTTTTTAAAAA[C/G]TATTTACAATGTGTG	114804
rs2289606	snp	G/T	0.321053	0.23969	intron-variant	RNF157	GRCh38.p7	17:76160616	TGCCATAGTTCATAT[G/T]GAATAAAACAGTAGA	114804
rs2290244	snp	C/T	0.0792508	0.182605	intron-variant	RNF157	GRCh38.p7	17:76162486	GAAATCGTAAGCCAG[C/T]GTCCAGAAATTTAGC	114804
rs2410923	snp	A/G	0.0607341	0.163335	intron-variant	RNF157	GRCh38.p7	17:76231287	tacaggcgtgcagcc[A/G]tgcccggccTCttgc	114804
rs2585734	snp	A/G	0	0			GRCh38.p7	17:76179722	AGATCTCTGGTTTTA[A/G]GTTGAAATAAGATAC	114804
rs2585735	snp	C/T	0.431916	0.171483			GRCh38.p7	17:76153219	TGATTGTTTCTCCCA[C/T]AGAATATTTGCTTCT	114804
rs2585736	snp	C/G	0.0337553	0.125452			GRCh38.p7	17:76152680	AGCAGCAGACAGAAA[C/G]GGCTCTAGGGAAACA	114804
rs2585737	snp	A/C	0.438246	0.16451			GRCh38.p7	17:76151543	TCCGGGTTTCACGAC[A/C]GAAATTGTCCTTCAC	114804
rs2585738	snp	C/T	0.457969	0.138741			GRCh38.p7	17:76150652	TTAACTGGCATCCTC[C/T]GTCAGTAGTTGGGTG	114804
rs2598424	snp	A/G	0.436692	0.166271			GRCh38.p7	17:76152997	ACTCAGGTCTCATAA[A/G]GAAGGAAATCATAAT	114804
rs2598425	snp	A/G	0.417683	0.185425			GRCh38.p7	17:76146810	TGGTCGGCCTTGTCC[A/G]CTGAACAGGTCCTCC	114804
rs2598426	snp	G/T	0.179425	0.239831			GRCh38.p7	17:76146141	GAAGTGAGCCCACAG[G/T]AGGCTGTGGAGGATT	114804
rs2598427	snp	C/T	0.458545	0.137872			GRCh38.p7	17:76143613	ATGGAGAGGGGGGCC[C/T]GTCGTCCAACCCTCT	114804
rs2598449	snp	A/G	0	0			GRCh38.p7	17:76179784	TCTTGGTCCCAAGAA[A/G]GCATTAGTTTTCTTT	114804
rs3075396	in-del	-/GA	0.375	0.216506	intron-variant	RNF157	GRCh38.p7	17:76238419	GTTAAACTTTTAAAA[-/GA]CTGGTAGAGAGGAGA	114804
rs3744036	snp	A/T	0.268936	0.249282	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145404	CCTTTGGCCAAATCC[A/T]GATGGTGTCTCCAGC	114804
rs3816427	snp	A/G	0.320575	0.239832	intron-variant	RNF157	GRCh38.p7	17:76163060	ATATTTTCCCTTCCC[A/G]TCTTTTTCCTTGCCA	114804
rs3859178	snp	C/T	0.499673	0.0127754	intron-variant	RNF157	GRCh38.p7	17:76217694	GTGAGTGACGTGTTT[C/T]TCCTGGTAACAAATA	114804
rs3859179	snp	C/T	0.0607341	0.163335	intron-variant	RNF157	GRCh38.p7	17:76231538	CCTAACCTCAGGTGA[C/T]CTTCTGGCCTTGGCC	114804
rs3859180	snp	C/T	0.409382	0.192607	intron-variant	RNF157	GRCh38.p7	17:76238167	TCCTTTCAGGACTAA[C/T]ACTGTAATCCCATAA	114804
rs3859181	snp	A/G	0.499793	0.0101816	intron-variant	RNF157	GRCh38.p7	17:76238577	TGTTAAGTCCCACAT[A/G]TGAAAGAGCGGTGAA	114804
rs4102459	snp	A/G	0	0	intron-variant	RNF157	GRCh38.p7	17:76226235	TGGATATCACTGAAG[A/G]AGATAGGAAGCCGGA	114804
rs4102460	snp	A/G	0	0	intron-variant	RNF157	GRCh38.p7	17:76226222	AGAAGATAGGAAGCC[A/G]GACTCCACTGCTTAC	114804
rs4102461	snp	A/C	0	0	intron-variant	RNF157	GRCh38.p7	17:76226217	ATAGGAAGCCGGACT[A/C]CACTGCTTACGTTGC	114804
rs4143087	snp	C/G	0	0	intron-variant	RNF157	GRCh38.p7	17:76175899	TGTTTCATTGCCACA[C/G]ttatcatcaaatata	114804
rs4316786	snp	A/G	0.0685596	0.171987	intron-variant	RNF157	GRCh38.p7	17:76205427	ataagccgccatgcc[A/G]ggcACATTTTAGTTC	114804
rs4505373	snp	G/T	0.481396	0.0946345	intron-variant	RNF157	GRCh38.p7	17:76208511	aaaagcttagaacaa[G/T]cagccctggcaaaaa	114804
rs4525514	snp	C/T	0.474091	0.11083	intron-variant	RNF157	GRCh38.p7	17:76198278	GAGAGCCTGTTGATA[C/T]AGGGACATTCTCTTA	114804
rs4788915	snp	C/T	0.141258	0.225111	intron-variant	RNF157	GRCh38.p7	17:76162720	TTTGGTAACCAAGGA[C/T]TACCGATTCATAATG	114804
rs4788916	snp	C/T	0.428333	0.175206	intron-variant	RNF157	GRCh38.p7	17:76173142	ATACAAAAAATTAGC[C/T]GGACGTGGTGGCGGG	114804
rs4789246	snp	A/C	0.111928	0.208413	intron-variant	RNF157	GRCh38.p7	17:76157883	ATGGGCCTCCCGACA[A/C]CCCCCACTTACCCCC	114804
rs4789247	snp	C/T	0.428786	0.174744	intron-variant	RNF157	GRCh38.p7	17:76173012	AAAAAGAAGGCTGGG[C/T]GCGGTGGCTCACGCC	114804
rs4789248	snp	A/G	0.0260105	0.111035	intron-variant	RNF157	GRCh38.p7	17:76176954	GGTTCTGCGCAGCCC[A/G]TCTGGGGCTGCGCCC	114804
rs4789249	snp	C/T	0.452597	0.146474	intron-variant	RNF157	GRCh38.p7	17:76187477	gcatgagccacggcg[C/T]ctggccAGGATTTTA	114804
rs4789250	snp	A/G	0.477515	0.103619	intron-variant	RNF157	GRCh38.p7	17:76194754	GGCACGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	114804
rs4789251	snp	C/T	0.48178	0.0936921	intron-variant	RNF157	GRCh38.p7	17:76202737	AGTGGCCAATCGAGG[C/T]TTCAAACAAGTCACA	114804
rs4789252	snp	A/C	0.247621	0.249989	intron-variant	RNF157	GRCh38.p7	17:76223011	ttctcctgcctcagc[A/C]ttccgagtagctggg	114804
rs4789253	snp	A/G	0.247905	0.249991	intron-variant	RNF157	GRCh38.p7	17:76224510	CTTTAGATCACAAAA[A/G]TAAGAAGAAAACTAG	114804
rs4789254	snp	A/T	0.25801	0.249872	intron-variant	RNF157	GRCh38.p7	17:76224682	GGTCTTACGCCACAC[A/T]TGAAATACACTAACA	114804
rs4789255	snp	A/G	0.499713	0.0119774	intron-variant	RNF157	GRCh38.p7	17:76224830	catgtagcccagccc[A/G]tggggcgtgggttgt	114804
rs4789256	snp	C/T	0.247905	0.249991	intron-variant	RNF157	GRCh38.p7	17:76225040	agccgggtatggtgg[C/T]gggcatctgtaatcc	114804
rs5822121	in-del	-/GT			intron-variant	RNF157	GRCh38.p7	17:76182482	TGTGTGTGTGTGTGT[-/GT]ATCAATCACATGTCC	114804
rs5822122	in-del	-/AG	0.495999	0.0445491	intron-variant	RNF157	GRCh38.p7	17:76238418	AGTTAAACTTTTAAA[-/AG]ACTGGTAGAGAGGAG	114804
rs6416850	snp	C/T	0.329084	0.237162	intron-variant	RNF157	GRCh38.p7	17:76201162	TTAAAAATGAAAACA[C/T]GTTCACTGGAAAAAA	114804
rs6501860	snp	C/G	0.329084	0.237162	intron-variant	RNF157	GRCh38.p7	17:76200904	GAGCTCCCTGACTCT[C/G]CTCCTCCCCATGCTT	114804
rs6501861	snp	C/T	0.330714	0.236612	intron-variant	RNF157	GRCh38.p7	17:76201251	agcactttgggaggc[C/T]gaggcaggaggattg	114804
rs6501862	snp	C/G	0.258288	0.249863	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213651	ctaatgaattaacca[C/G]tgcctggcagcccct	114804
rs6501863	snp	A/G	0.258288	0.249863	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213858	aaggactggttcaga[A/G]agcttccaaacaggg	114804
rs6501864	snp	C/T	0.25801	0.249872	intron-variant	RNF157	GRCh38.p7	17:76222480	aattttaaaaaaTCA[C/T]ATGGGGAGGAAGAAT	114804
rs6501865	snp	A/G	0.247053	0.249983	intron-variant	RNF157	GRCh38.p7	17:76223440	tgatccatccgcctc[A/G]gcctcccaaagtgct	114804
rs6501867	snp	C/G	0.25045	0.25	intron-variant	RNF157	GRCh38.p7	17:76226266	CTTCACTGCCCAGCT[C/G]TAAACTAAAGGAATG	114804
rs6501868	snp	A/G	0.499713	0.0119774	intron-variant	RNF157	GRCh38.p7	17:76226409	ACCATCTGGGGGGGC[A/G]CCTTATTAGTCTCCT	114804
rs6501869	snp	A/C	0.248755	0.249997	intron-variant	RNF157	GRCh38.p7	17:76235083	ttatatgcatagtaa[A/C]ttttaaaatagggta	114804
rs7207415	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76222179	gaagcaaccccgtct[C/T]tactaaaaatacaaa	114804
rs7208373	snp	C/T	0.0681886	0.171594	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150583	CAAGTAAGGGGTTGA[C/T]CAGGGTAGAGCTGCC	114804
rs7210049	snp	C/T	0.464416	0.128553	intron-variant	RNF157	GRCh38.p7	17:76226239	GCTTCCTATCTTCTT[C/T]AGTGATATCCACTTC	114804
rs7210745	snp	C/T	0.249603	0.25	intron-variant	RNF157	GRCh38.p7	17:76234554	cattttttaaaatta[C/T]agccatcctagtggg	114804
rs7210831	snp	A/G	0.25801	0.249872	intron-variant	RNF157	GRCh38.p7	17:76217865	CTTTGCAGGCTTTAA[A/G]AAGTCACATCATACA	114804
rs7214563	snp	C/T	0.279195	0.248289	intron-variant	RNF157	GRCh38.p7	17:76218195	aaagaaagaaaggca[C/T]ccaggcaaaaagtca	114804
rs7217334	snp	C/T	0.258288	0.249863	intron-variant	RNF157	GRCh38.p7	17:76221798	gtgaggtataatgtg[C/T]ccgacatatgtcctt	114804
rs7220727	snp	C/G	0.24932	0.249999	intron-variant	RNF157	GRCh38.p7	17:76237170	CCCAAGTCTCAACTT[C/G]AAATCTGCCATTCTT	114804
rs7221261	snp	A/G	0.111928	0.208413	intron-variant	RNF157	GRCh38.p7	17:76172556	agatcgcagtgagcc[A/G]agatcgtgccattgc	114804
rs7225367	snp	A/G	0.419296	0.183954	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241453	GTGTTTTTTTTCCTG[A/G]GAGAGTGGACTGATC	114804
rs7225664	snp	C/T	0.0349115	0.127424	intron-variant	RNF157	GRCh38.p7	17:76234740	tgagcatatgagttc[C/T]ttatatattctagat	114804
rs7225796	snp	A/C	0.0836354	0.186609	intron-variant	RNF157	GRCh38.p7	17:76206787	ctcaaaaaacaaaca[A/C]agaaaaCAGTGAAGA	114804
rs7225855	snp	C/T	0.499703	0.0121769	intron-variant	RNF157	GRCh38.p7	17:76228324	CCTTCTTCCTTGTGG[C/T]GCTCTCAGAACCCTT	114804
rs7359559	snp	A/G	0	0	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151689	CATGATCCTGTGTAA[A/G]GCATTACCTAGATTT	114804
rs7359560	snp	A/G	0	0	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151730	CATGAGGAGGAATAA[A/G]GGGCACTCTGACAAC	114804
rs7502444	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76199474	gcccaggctggtctt[A/G]aactcctgggctcaa	114804
rs7502723	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76199589	aaaaaaaaaaaaaaa[A/T]aaagaaCAGCTGGCA	114804
rs8067190	snp	A/T	0.0298908	0.118541	intron-variant	RNF157	GRCh38.p7	17:76176426	GCAAATTAAAAAAAA[A/T]TTTTTTTCTGCTCTT	114804
rs8067947	snp	C/T	0.488302	0.0755777	intron-variant	RNF157	GRCh38.p7	17:76199070	ACAATGGGTATTCCA[C/T]AGAATGTAAATGATT	114804
rs8068111	snp	C/T	0.0429648	0.14013	intron-variant	RNF157	GRCh38.p7	17:76220331	atatattaagcttca[C/T]caggataataagggc	114804
rs8068137	snp	C/T	0.487241	0.0788465	intron-variant	RNF157	GRCh38.p7	17:76169108	atttccttcctttta[C/T]attctctgttctctg	114804
rs8068290	snp	C/T	0.247905	0.249991	intron-variant	RNF157	GRCh38.p7	17:76220435	atgctagtaaaccaa[C/T]tcattattttggaaa	114804
rs8068421	snp	A/G	0.0995161	0.199636	intron-variant	RNF157	GRCh38.p7	17:76199020	CAGGGACTGCATTTC[A/G]TCGGTATTTCTAGTG	114804
rs8068624	snp	A/T	0.442926	0.158996	intron-variant	RNF157	GRCh38.p7	17:76220658	tacaaatttattatt[A/T]ttttttttttagtta	114804
rs8070392	snp	C/T	0.49823	0.0296997	intron-variant	RNF157	GRCh38.p7	17:76210945	gagcagctgggatta[C/T]aggggtgtgccacca	114804
rs8070711	snp	C/G	0.158302	0.232576	intron-variant	RNF157	GRCh38.p7	17:76240034	CTCGAAGACCGTTTC[C/G]GAGCGTCCGCAACCA	114804
rs8071198	snp	A/T	0.454061	0.144427	intron-variant	RNF157	GRCh38.p7	17:76174076	CTGGAGAATTAATAA[A/T]AAAAAAAAAAACCGC	114804
rs8072857	snp	C/T	0.014814	0.0847794	intron-variant	RNF157	GRCh38.p7	17:76162485	CGCTAAATTTCTGGA[C/T]GCTGGCTTACGATTT	114804
rs8074389	snp	C/T	0.258843	0.249844	intron-variant	RNF157	GRCh38.p7	17:76230379	CACCCAGGCTAAAAA[C/T]GTCAGTCATCAAAGA	114804
rs8074651	snp	A/G	0.473818	0.111381	intron-variant	RNF157	GRCh38.p7	17:76187436	tgatccacccacctc[A/G]gccacccaaagtgct	114804
rs8076990	snp	C/T	0.448452	0.152042	intron-variant	RNF157	GRCh38.p7	17:76169520	taagtgatcctcctg[C/T]tttggcctcccaaag	114804
rs8077046	snp	A/G	0.433236	0.170072	intron-variant	RNF157	GRCh38.p7	17:76170788	actaagtcatttaac[A/G]ttcactatgtgtttc	114804
rs8077453	snp	G/T	0.174932	0.238463	intron-variant	RNF157	GRCh38.p7	17:76193952	GCTACCACTTCTCTG[G/T]GGTACACGTCCACAA	114804
rs8079508	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76209921	cacaccaccacgccc[A/G]gctaatttttgtatt	114804
rs8081775	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76234022	catttctccctctcc[C/T]cagcctctggcagcc	114804
rs8081930	snp	C/T	0.0704125	0.17392	intron-variant	RNF157	GRCh38.p7	17:76234101	tggatttgcctcttc[C/T]gggcatttcttataa	114804
rs9302997	snp	A/T	0.407674	0.194008	intron-variant	RNF157	GRCh38.p7	17:76215763	CAAGCAGGAAAACAT[A/T]CTTTGAGAGTAATAA	114804
rs9302998	snp	A/G	0.4944	0.0526182	intron-variant	RNF157	GRCh38.p7	17:76215788	TAATAATGCAACCCA[A/G]ATCAAAGCAATCACT	114804
rs9891273	snp	G/T	0.318656	0.240388	intron-variant	RNF157	GRCh38.p7	17:76169968	aagaatctgtggctg[G/T]ctgcttgtatttaag	114804
rs9891964	snp	A/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76208855	ggcaggcacctgtaa[A/T]cccagctagtcagga	114804
rs9892399	snp	C/T	0.317451	0.240729	intron-variant	RNF157	GRCh38.p7	17:76171024	cagcctcccaaatag[C/T]tgggattacaggtgc	114804
rs9893558	snp	G/T	0.433527	0.169758	intron-variant	RNF157	GRCh38.p7	17:76163682	ATATCCCACTCTCCG[G/T]TTTAACAGTCTGTTG	114804
rs9895378	snp	A/G	0.465473	0.126772	intron-variant	RNF157	GRCh38.p7	17:76210453	AAATTAGCCGGGTGT[A/G]GTGGCGGGTGCCTGT	114804
rs9895605	snp	A/G	0.487368	0.0784625	intron-variant	RNF157	GRCh38.p7	17:76210522	GTGAACCCGGGAGGC[A/G]GAGCTTTCAGTGAGC	114804
rs9896553	snp	C/T	0.499683	0.0125759	intron-variant	RNF157	GRCh38.p7	17:76216707	GTTCACAATATATTA[C/T]AATTAGACCCTTGTC	114804
rs9899673	snp	A/G	0.335788	0.23482	intron-variant	RNF157	GRCh38.p7	17:76180933	CAGCCTGTAAGTTCC[A/G]TGTGTATGCTGGAGG	114804
rs9900102	snp	C/T	0.474723	0.109542	intron-variant	RNF157	GRCh38.p7	17:76194821	GAGATCGAGACCATC[C/T]TGGCTAACATGGTGA	114804
rs9900336	snp	C/G	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76194923	AGGAGGCTGAGGCAG[C/G]AGAATGGCGTGAACC	114804
rs9900975	snp	C/T	0.44768	0.153045	intron-variant	RNF157	GRCh38.p7	17:76210331	GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC	114804
rs9901220	snp	A/G	0.43309	0.17023	intron-variant	RNF157	GRCh38.p7	17:76239347	TGATACCACAATCCA[A/G]AGGCTAGAGACATTT	114804
rs9901431	snp	C/T	0.495927	0.0449436	intron-variant	RNF157	GRCh38.p7	17:76210557	ATCGTGCCACTGTAC[C/T]CCAGCCTGGGCGACA	114804
rs9903178	snp	A/C	0.40733	0.194287	intron-variant	RNF157	GRCh38.p7	17:76239124	ATCACCAAAATCTCC[A/C]TCGGGTCCTAAGCAG	114804
rs9904343	snp	A/C	0.421526	0.181876	intron-variant	RNF157	GRCh38.p7	17:76160251	ATCCTATTGTAAACA[A/C]GTTTTGATGAACATC	114804
rs9904681	snp	C/G	0.408359	0.193449	intron-variant	RNF157	GRCh38.p7	17:76226912	GCGCCATGGCTTAAG[C/G]CGCTGGGGGGTGCCG	114804
rs9908949	snp	C/T	0.318896	0.240319	intron-variant	RNF157	GRCh38.p7	17:76181305	TCTCCAATGGCGCCC[C/T]ATGCTTAGATGGCAG	114804
rs9909652	snp	C/T	0	0	intron-variant	RNF157	GRCh38.p7	17:76181574	TCAAAGATGTGTTAC[C/T]GCCAGATAGTTCTAA	114804
rs9911122	snp	A/G	0.431462	0.171979	intron-variant	RNF157	GRCh38.p7	17:76212343	AAGCTCCAAGTAGGA[A/G]TAAACTGATTACAGC	114804
rs9911230	snp	C/G	0	0	intron-variant	RNF157	GRCh38.p7	17:76170347	gatcctcccacttca[C/G]cctcccaagtagctg	114804
rs9911570	snp	C/T	0.407502	0.194147	intron-variant	RNF157	GRCh38.p7	17:76218471	catagcaagacctca[C/T]ctctacaataaaaaa	114804
rs9911832	snp	A/G	0.427119	0.176434	intron-variant	RNF157	GRCh38.p7	17:76193444	CTTGAAGTAAATACA[A/G]TTAGGATATATCTCA	114804
rs9912355	snp	C/G	0	0	intron-variant	RNF157	GRCh38.p7	17:76179249	aaaatgtagaactta[C/G]tcagcatggtggcac	114804
rs9912975	snp	C/T	0	0	missense, utr-variant-5-prime, nc-transcript-variant	RNF157	GRCh38.p7	17:76212405	TCAGATCGCTGTTCT[C/T]TCCAAACAGGTAACC	114804
rs9913054	snp	A/C	0.48155	0.0942576	intron-variant	RNF157	GRCh38.p7	17:76208942	TCGTGCCACTGCACT[A/C]CAGCTTGGGTGACAG	114804
rs9914821	snp	A/G	0.327914	0.237549	intron-variant	RNF157	GRCh38.p7	17:76193636	AGGGAAATGGAAGAC[A/G]CTGTCTAAGGTAACG	114804
rs9915751	snp	A/C/T	0.501732	0.215999	intron-variant	RNF157	GRCh38.p7	17:76179585	GTAGTCCCAGCTACT[A/C/T]GGGAGGCTGAGGCAG	114804
rs9916150	snp	A/C	0.407674	0.194008	intron-variant	RNF157	GRCh38.p7	17:76216219	GGACCACTGAGTTTC[A/C]AGTACCTGTGAGATC	114804
rs10048213	snp	A/T	0.375	0.216506	intron-variant	RNF157	GRCh38.p7	17:76202130	CTCTCTCTCTCTCTC[A/T]CACACACACACACAC	114804
rs10512605	snp	A/G	0.258288	0.249863	intron-variant	RNF157	GRCh38.p7	17:76216301	GGTCCTCTCTCGCTA[A/G]GTTCAATCATGGCCA	114804
rs10512606	snp	G/T	0.247905	0.249991	intron-variant	RNF157	GRCh38.p7	17:76215127	AAATTGCAACTGATT[G/T]AGGGAGTTTGTGTAT	114804
rs10512607	snp	A/G	0.407502	0.194147	intron-variant	RNF157	GRCh38.p7	17:76214971	CAGCTTACCTTCATG[A/G]GAGAATTAGATAATA	114804
rs10512608	snp	A/G	0.142272	0.225598	intron-variant	RNF157	GRCh38.p7	17:76174909	ATGGTTAATATATCA[A/G]TGAAAAAGTAAATTA	114804
rs10699377	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76208988	AAAAAAAAAAAAAAA[-/A]TTCATTTGCTATGTG	114804
rs11077805	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76169983	TCTGCTTGTATTTAA[C/G]ATATTTAAACTGCTG	114804
rs11077806	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76170166	AAGGCCTGGCTGCCA[G/T]CATTCTAGGGGCAGA	114804
rs11077807	snp	C/T	0.0189856	0.0955633	intron-variant	RNF157	GRCh38.p7	17:76182535	TGATTTCAAATATTA[C/T]ACTACTCCTACGGTT	114804
rs11077808	snp	A/C	0.391954	0.205789	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241244	TCGTGGAAACGGGAC[A/C]CCGGAAACTTTGGAA	114804
rs11366004	in-del	-/G			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153124	CCTCTTTTTTTCTCA[-/G]TGAAACAGAGAGAAG	114804
rs11392375	in-del	-/C	0.326506	0.238006	intron-variant	RNF157	GRCh38.p7	17:76197110	GGGGTGGATCACCCA[-/C]CAGCCAGATGGCAAT	114804
rs11439973	in-del	-/T	0	0	intron-variant	RNF157	GRCh38.p7	17:76209493	TGCGTTTTTTTTTTT[-/T]CTTTTTTAGCTCATC	114804
rs11491183	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76201350	AAAAAAGAGAAAAAG[A/G]AAAAATTTTAAATTA	114804
rs11491184	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76201356	GAGAAAAAGAAAAAA[A/T]TTTAAATTAGCTGTG	114804
rs11539879	snp	A/G	0.0725058	0.176056	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76166467	GCCGTGGTGGATGAA[A/G]GAGACGGTAGGGGCG	114804
rs11652973	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76195926	ttactattgccacgg[C/G]aacacctggaagtta	114804
rs11653252	snp	A/T			utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144345	ttttttttttctctg[A/T]cgcccaggctggagt	114804
rs11655525	snp	C/G	0.0970103	0.197722	intron-variant	RNF157	GRCh38.p7	17:76173601	CAAGCTCTGGGGCTG[C/G]CGGAAACTGCTGTAT	114804
rs11868301	snp	A/G	0.216349	0.247725	intron-variant	RNF157	GRCh38.p7	17:76203829	ctggagtgcagtggc[A/G]cgatctcggctcact	114804
rs12051808	snp	A/G	0.342358	0.232314	intron-variant	RNF157	GRCh38.p7	17:76195548	tatgcatacatatac[A/G]caacaaaatacatgt	114804
rs12103653	snp	A/T	0.49949	0.0159663	intron-variant	RNF157	GRCh38.p7	17:76239497	TCCGAGTAACTCTGA[A/T]ACTCAGATTCCCAAA	114804
rs12150140	snp	C/T	0.49423	0.0534032	intron-variant	RNF157	GRCh38.p7	17:76230716	GGTGGCAGGCACCTG[C/T]AATCCCAGCTACTCG	114804
rs12165062	snp	G/T	0	0	intron-variant	RNF157	GRCh38.p7	17:76158336	TGATGAGGCATGCAG[G/T]TAGGAGGGAAGTCCC	114804
rs12232523	snp	C/T	0.0189856	0.0955633	intron-variant	RNF157	GRCh38.p7	17:76234362	gtttttatgtgaatg[C/T]attttcttcattttt	114804
rs12449682	snp	C/T	0	0	intron-variant	RNF157	GRCh38.p7	17:76229320	GAGCTGGATTTTATC[C/T]TGATGCTGCTGCCTA	114804
rs12452812	snp	A/C	0.0023933	0.0345097	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144600	gcgtgagccaccgcg[A/C]ccggccAAGAGCTCC	114804
rs12453112	snp	A/G	0.0763149	0.179815	intron-variant	RNF157	GRCh38.p7	17:76208276	TTGAAGATCTACACA[A/G]TGGACTCACAAACAG	114804
rs12453778	snp	G/T	0.00318978	0.0398085	intron-variant	RNF157	GRCh38.p7	17:76188565	TTAAACAAGGTGCAA[G/T]CAAAGATGGTGCAAT	114804
rs12453957	snp	A/G	0	0	utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142598	GGGTACACAGATGGC[A/G]CAAGCAGTATACACA	114804
rs12601803	snp	C/T	0.406986	0.194565	intron-variant	RNF157	GRCh38.p7	17:76211803	GATGCAGAGAAGGTG[C/T]GCAATAGAAATTTAT	114804
rs12602521	snp	C/T	0.160609	0.233472	intron-variant	RNF157	GRCh38.p7	17:76188289	CACTGCCCCATGTGG[C/T]CACCCATCACTTCTC	114804
rs12604011	snp	C/T	0.174288	0.23826	intron-variant	RNF157	GRCh38.p7	17:76188343	TCCTTGAGCCACATC[C/T]TTCATCACCTCCAAT	114804
rs12937813	snp	C/T	0.181978	0.240568	intron-variant	RNF157	GRCh38.p7	17:76177054	AGGCCCAGGATCCAC[C/T]CTGTCCCAGACTGCC	114804
rs12938489	snp	C/T	0.176219	0.238865	intron-variant	RNF157	GRCh38.p7	17:76185006	CAGGTGATAAGGGTA[C/T]GAAAAACCTACCACA	114804
rs12942176	snp	A/G	0.464416	0.128553	intron-variant	RNF157	GRCh38.p7	17:76210036	GTGCTGGGATTACAG[A/G]CATGAGTCACCGTGC	114804
rs12944965	snp	C/T	0.178144	0.239451	intron-variant	RNF157	GRCh38.p7	17:76190349	tttttatatttttag[C/T]agagacggagtttcg	114804
rs12945842	snp	C/T	0.00755907	0.0610114	intron-variant	RNF157	GRCh38.p7	17:76191796	ATTAAAATGTAAAGA[C/T]AAAGTATATGTCTGA	114804
rs12949000	snp	C/T	0.437401	0.165472	intron-variant	RNF157	GRCh38.p7	17:76171241	tcacccagagtggag[C/T]gcagtggtacaatct	114804
rs12950642	snp	C/T	0.479904	0.0982045	intron-variant	RNF157	GRCh38.p7	17:76210259	TTTTGAAAAGTGTAC[C/T]ACTGGACGAAAAATT	114804
rs12952480	snp	C/T	0	0	intron-variant	RNF157	GRCh38.p7	17:76189835	ggaggagaaCACAAA[C/T]AAAAACAACTGAAGG	114804
rs16968610	snp	A/G	0.0295035	0.117819	intron-variant	RNF157	GRCh38.p7	17:76157585	ACACAGCAATTTATC[A/G]TCTCTGTTTTGGGCA	114804
rs16968638	snp	C/G	0.31419	0.241644	intron-variant	RNF157	GRCh38.p7	17:76164833	ATGACAAGGAAGGGA[C/G]GGTAATAAAGCACCA	114804
rs16968642	snp	C/T	0.305986	0.243651	intron-variant	RNF157	GRCh38.p7	17:76165452	TACATGTGTCTCACA[C/T]GAAAGAAAGGGCTAA	114804
rs16968673	snp	A/T	0.194278	0.243711	intron-variant	RNF157	GRCh38.p7	17:76172750	CTTCCTTGCCTATTC[A/T]GAAAAATCTGGGACC	114804
rs16968692	snp	A/C	0.309648	0.24278	intron-variant	RNF157	GRCh38.p7	17:76182036	CACAGTGAAGAGTCA[A/C]GCAAACCTCTCTTAG	114804
rs16968696	snp	C/T	0.317692	0.240661	intron-variant	RNF157	GRCh38.p7	17:76182257	TCAGGCGTTTGCTGA[C/T]GAAGGCTCTGTGTGT	114804
rs16968702	snp	A/G	0.33533	0.234987	intron-variant	RNF157	GRCh38.p7	17:76185381	TAAGTTGAGTTAAAA[A/G]GAGAAAAGCGTGCTC	114804
rs16968719	snp	G/T	0.0193772	0.0965046	intron-variant	RNF157	GRCh38.p7	17:76194340	GTAAAATAGCCAAAG[G/T]CCTCATTCAGTTCGC	114804
rs16968732	snp	A/G	0.00755907	0.0610114	intron-variant	RNF157	GRCh38.p7	17:76214667	CACCTCAAATTCATT[A/G]ACAGTGCTAATGGCC	114804
rs16968738	snp	A/G	0.030665	0.119967	intron-variant	RNF157	GRCh38.p7	17:76217760	GCCTATTTGCTAACG[A/G]GAAAAAAACATATGT	114804
rs16968746	snp	A/G	0.00795532	0.062565	intron-variant	RNF157	GRCh38.p7	17:76227988	TGAATGTCCAGATTT[A/G]ATTAACTGTTTCCCT	114804
rs17501563	snp	C/T	0.0103295	0.0711199	intron-variant	RNF157	GRCh38.p7	17:76178840	CTTTTTTTTTTCCAG[C/T]AACTAACATGTCTTA	114804
rs17508653	snp	C/T	0.0584853	0.160693	intron-variant	RNF157	GRCh38.p7	17:76222525	TTATAATGCTGTCAT[C/T]TGAATTTTTATTTTA	114804
rs28494893	snp	C/G	0.4087	0.193169	intron-variant	RNF157	GRCh38.p7	17:76231350	TATTGAGTTGTAAGA[C/G]TTCTTAATATTGATA	114804
rs28583086	snp	A/G	0.4087	0.193169	intron-variant	RNF157	GRCh38.p7	17:76231249	TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT	114804
rs28614026	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76190574	TGCCACTGCACTCCA[A/G]CCTGGGTGACAGAGT	114804
rs28672851	snp	A/G	0.00115498	0.0240033	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76158444	CTGTGTCTCCGACTC[A/G]CTGCAGGAATGCTCA	114804
rs28698007	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76206507	ACTTAAGACAGTATT[A/T]AAAAACCAGTGAAGA	114804
rs34014361	snp	C/T	0.145305	0.227022	intron-variant	RNF157	GRCh38.p7	17:76191595	GACAGAGCAAGACTC[C/T]GCCTCAAAAAAAAAA	114804
rs34151599	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76199592	AAAAAAAAAAAAAAA[-/A]GAACAGCTGGCAGGA	114804
rs34173493	in-del	-/G			intron-variant	RNF157	GRCh38.p7	17:76212230	AGGAGGCTGCAGTTT[-/G]GTCTTCTAGTGCATC	114804
rs34189763	in-del	-/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76232927	ATATTTTTTTTTTTT[-/T]GAGACACAGTCTTGC	114804
rs34213868	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76217863	TTCTTTGCAGGCTTT[-/A]AAAAGTCACATCATA	114804
rs34244254	snp	A/G	0.00557542	0.0525036	intron-variant	RNF157	GRCh38.p7	17:76157244	GTGCCGGGATTCCAG[A/G]CGTGAGCCTCCGCGC	114804
rs34250119	snp	C/T	0.0119091	0.0762411	intron-variant	RNF157	GRCh38.p7	17:76176068	GTGGGCTGCTACCCA[C/T]CAAAGTTTGTGCCTT	114804
rs34273775	in-del	-/C			intron-variant	RNF157	GRCh38.p7	17:76156630	TGTGACATGGGGACA[-/C]CCCCAGGTTTCCCCA	114804
rs34317178	in-del	-/G			intron-variant	RNF157	GRCh38.p7	17:76188850	CGGACCATGTAAACA[-/G]GGGCTGATATCAACA	114804
rs34378398	in-del	-/C			intron-variant	RNF157	GRCh38.p7	17:76182860	GATATATAGGATATA[-/C]TATATCCTATATATC	114804
rs34425847	in-del	-/C			frameshift-variant, nc-transcript-variant	RNF157	GRCh38.p7	17:76167675	CATTCTGGAACTCTT[-/C]CCGTGGCCTGGTAAT	114804
rs34431718	in-del	-/C			intron-variant	RNF157	GRCh38.p7	17:76205606	GTGTGTGCCTGTAGT[-/C]CCCAGCTACTTGGGA	114804
rs34435056	snp	A/T	0.407845	0.193868	intron-variant	RNF157	GRCh38.p7	17:76222399	GATTGTGCAACACTG[A/T]GAATGTTCAAAATGC	114804
rs34517490	snp	C/G			upstream-variant-2KB	RNF157	GRCh38.p7	17:76240672	GCGGCCCAGGGCCTC[C/G]CGGCGGGGGCGTGGG	114804
rs34522999	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76233539	TATGTCTATGATCCA[-/T]TTTTATTTTTTTATT	114804
rs34641812	in-del	-/A			intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147417	GCCGCCGCCACCACC[-/A]AGCAAGCCATGGAAT	114804
rs34706600	in-del	-/T	0.148661	0.22854	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150140	ATAGTCTCACACATA[-/T]TTTTTTTCTTGGAAA	114804
rs34766219	in-del	-/C			utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76144913	AGCCTTCTTGTTCTA[-/C]CCCCTAAGGAGAAAA	114804
rs34802414	in-del	-/G			intron-variant	RNF157	GRCh38.p7	17:76212216	ATCCCATACAACCAA[-/G]GGAGGCTGCAGTTTG	114804
rs34816147	in-del	-/T	0.318656	0.240388	intron-variant	RNF157	GRCh38.p7	17:76192842	TCCCACTTTCTTTCC[-/T]TTTTTTTTTTTTTTT	114804
rs34844187	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76221765	CAAATGTCAAACAAC[-/A]AAATGGGTAAACAAA	114804
rs34871096	in-del	-/G			intron-variant	RNF157	GRCh38.p7	17:76204917	GCCTCCTGAGTAGCT[-/G]GGGATTACAAGCACC	114804
rs34888046	in-del	-/A	0.493658	0.0559517	intron-variant	RNF157	GRCh38.p7	17:76220386	TTCGTAATGATATCT[-/A]AAAAAAAAAAAAAAA	114804
rs34995888	snp	A/G	0.454302	0.144085	intron-variant	RNF157	GRCh38.p7	17:76170182	CATTCTAGGGGCAGA[A/G]TGGAGAGGCAGCTGG	114804
rs35036329	snp	C/T	0.0209421	0.100162	intron-variant	RNF157	GRCh38.p7	17:76227605	GGTAGTGGCCCGGCA[C/T]GGTGGCTCACGCCTG	114804
rs35052049	in-del	-/C			intron-variant	RNF157	GRCh38.p7	17:76211035	GTCTTGAGCTCCCAA[-/C]CTCAGGTGATCTGTC	114804
rs35164451	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76165684	TACTTTTTTTTTTTT[-/T]GAGACAGAGTCTGGC	114804
rs35184382	in-del	-/C			intron-variant	RNF157	GRCh38.p7	17:76169906	TTTTAAAATGTTGGT[-/C]TTGTTTTGCTACTGT	114804
rs35229207	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76160365	TGATATATACTGCTG[-/T]TTTCTGCTGTTTTTT	114804
rs35280721	in-del	-/G			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152872	CCTTGGGTGTGAGCT[-/G]GGGTGTGTTTAGGAC	114804
rs35297368	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76172608	GCAAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA	114804
rs35330664	in-del	-/A	0	0	intron-variant	RNF157	GRCh38.p7	17:76224720	TTTAAAAAAAAAAAA[-/A]GAAAGAAACTGCAAA	114804
rs35372072	in-del	-/A	0.418974	0.184249	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212541	TAGTAAAAAAAAAAA[-/A]GCTGATTTTTAAAAT	114804
rs35372216	in-del	-/C			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145634	TGTTTTGCGAACTTA[-/C]CCCTGGGATCCACTT	114804
rs35451973	in-del	-/G			intron-variant	RNF157	GRCh38.p7	17:76221818	ATATGTCCTTACAAC[-/G]GGAATATTATTCAGC	114804
rs35453352	snp	C/T	0.375	0.216506	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213543	CCACTACACTCCAGC[C/T]TAGGTGACAGAGCAA	114804
rs35564567	in-del	-/TT			intron-variant	RNF157	GRCh38.p7	17:76163191	CTTGGCCCTGTTTCC[-/TT]TTTTTTTTTTTTTTT	114804
rs35629624	in-del	-/A			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150033	GCGAGACTCTGTCTC[-/A]AAAAAAACAAAAAAC	114804
rs35768652	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76236792	TACTATATAGTTGTT[-/A]AAAAGCACAAAGAAA	114804
rs35777038	snp	C/T	0.222035	0.248431	intron-variant	RNF157	GRCh38.p7	17:76157000	GGAGTCTCGCTCTGT[C/T]GCCCAGCCCAGGCTG	114804
rs35782875	in-del	-/A	0.499515	0.0155675	intron-variant	RNF157	GRCh38.p7	17:76220958	GTGAGATGCTGTCTC[-/A]AAAAAAAAAAAAAAA	114804
rs35783403	snp	C/T	0.0295035	0.117819	intron-variant	RNF157	GRCh38.p7	17:76215871	TCTGATACAGTGATA[C/T]AACAGCAGAATTCAT	114804
rs35814255	in-del	-/C			intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154430	TATCTAACTCCAGGG[-/C]CCTACGTTAATAGCA	114804
rs35822083	in-del	-/C	0.0737376	0.17729	intron-variant	RNF157	GRCh38.p7	17:76166268	GTGTGAGCCACTGTG[-/C]CCAGCCAAACCCACA	114804
rs35838823	in-del	-/G			intron-variant	RNF157	GRCh38.p7	17:76184531	GTGAAGTGAATACAA[-/G]ATTTGCCTATTTACC	114804
rs35839727	in-del	-/TAAA			intron-variant	RNF157	GRCh38.p7	17:76205723	GCAAGACTCCATCTC[-/TAAA]TAAATAAATAAATAA	114804
rs35848509	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76203452	AGGAAAAGTAAAAAC[-/T]TTTTTTTTTTTTTTT	114804
rs35859645	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76171522	CATGTTTATAATTAC[-/T]TTAATGGGGTTTTCA	114804
rs35944957	in-del	-/C			intron-variant	RNF157	GRCh38.p7	17:76200325	AGGCAGGAGCAACCC[-/C]AAGTGTCTGTCTATT	114804
rs35953149	in-del	-/G			intron-variant	RNF157	GRCh38.p7	17:76218398	CAATCCCAGTACTTT[-/G]GGGAGGCCAAGGCAG	114804
rs35964589	snp	C/T	0.177182	0.23916	intron-variant	RNF157	GRCh38.p7	17:76177293	AAGCTCTTGGAGACA[C/T]GGAAAAGCCCTCCCA	114804
rs36007927	in-del	-/G			intron-variant	RNF157	GRCh38.p7	17:76223320	GCCTTGCAAGTAGCT[-/G]GGGATTACAGGCATG	114804
rs36009510	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76181907	GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	114804
rs36032105	snp	C/G	0.162581	0.234218	intron-variant	RNF157	GRCh38.p7	17:76177313	AAGCCCTCCCACCCC[C/G]CCGCCCCAGCAGGCT	114804
rs36032974	in-del	-/G			intron-variant	RNF157	GRCh38.p7	17:76220348	GGATAATAAGGGCAA[-/G]GGAATAAGTCTAAGT	114804
rs36035560	snp	A/C			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153123	CCCTCTTTTTTTCTC[A/C]GTGAAACAGAGAGAA	114804
rs36072890	in-del	-/C			frameshift-variant, nc-transcript-variant	RNF157	GRCh38.p7	17:76161938	GCAGAATCAAGGTGT[-/C]CCCGGACATCCGAGA	114804
rs41340049	snp	A/G	0.084728	0.187577	intron-variant	RNF157	GRCh38.p7	17:76202790	CATGGACCAATTTAT[A/G]ACCTTGCAGAGAAGG	114804
rs55646865	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76234306	TGATGAACATTTGGG[G/T]TATTTCCACATTTTA	114804
rs55685190	snp	G/T	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76233845	GCCCCATTTTGAAAA[G/T]AGCTTTGTGGAGATA	114804
rs55728925	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76234303	GGTTGATGAACATTT[G/T]GGTTATTTCCACATT	114804
rs55760274	in-del	-/TT	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76168441	TATTTTTTTTTTTTT[-/TT]CTTCCAGTTGCGTAG	114804
rs55766415	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76186716	AGGCCGAGGCGGGCA[C/G]ATAACCTGAGGTCAG	114804
rs55777329	snp	A/G	0.312593	0.242037	intron-variant	RNF157	GRCh38.p7	17:76159018	GTTCCTTCAGTCTTC[A/G]GACTAAGCAATGCTC	114804
rs55846908	snp	C/T	0.0283406	0.115616	intron-variant	RNF157	GRCh38.p7	17:76168770	TGTCCTGCCAGCTTC[C/T]TGAAAAAGGGTGTGT	114804
rs55876221	snp	C/G	0.193028	0.243422	intron-variant	RNF157	GRCh38.p7	17:76185468	AGTGGTCAGAGATTA[C/G]TCCTTTCTTTTTTTT	114804
rs55948491	snp	A/G	0.205417	0.245993	intron-variant	RNF157	GRCh38.p7	17:76199171	TTGGCAACATGTTAT[A/G]ATCATTTAAGAAAAC	114804
rs56009254	snp	A/G	0.0221141	0.102801	intron-variant	RNF157	GRCh38.p7	17:76179023	CCTTTCTAAAGTCAA[A/G]ACATCAGATAAATGT	114804
rs56089770	snp	C/T			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153936	CTGAGAATGCCAGAA[C/T]AGCTCTGTGGGGCTC	114804
rs56113254	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76225724	ACTCTATGTACAAGC[A/G]CGTTGACACTCCTGA	114804
rs56130819	snp	A/T	0.247905	0.249991	intron-variant	RNF157	GRCh38.p7	17:76216579	TGGTGAGGCTCTGTC[A/T]CTGTATATTTAAAAA	114804
rs56231427	in-del	-/TT	0	0	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76148282	TTTTTTTTTTTTTTT[-/TT]GAGACAGGGTCTCTT	114804
rs56257305	snp	A/G	0.248755	0.249997	intron-variant	RNF157	GRCh38.p7	17:76211862	CTCATATCAACTCAT[A/G]TATCAAGAGAAAAAT	114804
rs56280453	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76210376	AGGTGGGCGGATCAC[A/G]AGGTCAGATCGAGAC	114804
rs56280493	snp	C/T	0.177824	0.239355	intron-variant	RNF157	GRCh38.p7	17:76163489	GATGAGCCATCAAGC[C/T]CGGCCAGCCCTGTTT	114804
rs56288526	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76168174	CCACGTTTCTAAAAA[-/A]TATACTTGGGTTACT	114804
rs56722925	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76182795	TATATATATGAGAGA[G/T]ATATATATGAGAGAG	114804
rs56897111	snp	C/G	0.0429648	0.14013	intron-variant	RNF157	GRCh38.p7	17:76182129	TCCTGGGACTGGGCT[C/G]CTGTGTCTGTCCTGA	114804
rs57077214	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76195443	AGTGGGAAAAAAAAA[-/A]TTGGTAGAATCACTT	114804
rs57193564	snp	C/T			intron-variant, upstream-variant-2KB, downstream-variant-500B	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142382	CTCCCACTCCTCCAA[C/T]TCCAGATCCTCTTGA	114804
rs57614769	snp	C/T	0.0479149	0.147179	intron-variant	RNF157	GRCh38.p7	17:76203875	CGGGTTCACGCCATT[C/T]TCCTGCCTCAGCCTC	114804
rs57882329	snp	C/T	0.0314385	0.121371	intron-variant	RNF157	GRCh38.p7	17:76220597	GGGAAGGCCTTGAGC[C/T]CAGAAGTTTGAGACC	114804
rs57938794	snp	G/T	0.205417	0.245993	intron-variant	RNF157	GRCh38.p7	17:76197701	AGCCTCCCGAGTGCT[G/T]GGATTACAGATGTGC	114804
rs58003444	snp	C/T	0.329783	0.236927	intron-variant	RNF157	GRCh38.p7	17:76208370	TCTGGAGCCAGACTG[C/T]TAGGTTCCAATCCTG	114804
rs58097008	snp	A/G	0.0659589	0.169201	intron-variant	RNF157	GRCh38.p7	17:76208105	CATTTTATATTTTGT[A/G]GAGATGAGGGTCTCG	114804
rs58115413	snp	C/T	0.0248432	0.108648	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145140	GGAGGGTAAAAAGTC[C/T]CCAGCATCTTGCTGA	114804
rs58254164	snp	C/T	0.0162398	0.0886349	intron-variant	RNF157	GRCh38.p7	17:76174969	AATTACAAAGTAATA[C/T]ATGTTTAAGCAGAAA	114804
rs58382842	snp	C/T	0.227664	0.249	intron-variant	RNF157	GRCh38.p7	17:76185650	AATTTTTTGTATTTT[C/T]AGTAGAGACGGGGTT	114804
rs58418601	snp	A/G	0.0158469	0.0875917	intron-variant	RNF157	GRCh38.p7	17:76166920	GGCCTTCAAGCATCC[A/G]AGCAGCCCCTTTGCT	114804
rs58492014	snp	A/G	0.32768	0.237625	intron-variant	RNF157	GRCh38.p7	17:76200191	AGCTTGCAGTGAGCC[A/G]AGATCGCGCCACTCC	114804
rs58622457	in-del	-/AA			intron-variant	RNF157	GRCh38.p7	17:76199591	AAAAAAAAAAAAAAA[-/AA]GAACAGCTGGCAGGA	114804
rs58839658	snp	A/G	0.32768	0.237625	intron-variant	RNF157	GRCh38.p7	17:76198279	AGAGCCTGTTGATAC[A/G]GGGACATTCTCTTAT	114804
rs58914264	in-del	-/TAAA	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76205763	AAATAAATAAATAAA[-/TAAA]ATAATAATGCCAGCT	114804
rs58928276	in-del	-/AAAAAA			intron-variant	RNF157	GRCh38.p7	17:76172628	AAAAAAAAAAAAAAA[-/AAAAAA]GGCGAGACTCTGTCT	114804
rs59023506	snp	G/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76200934	TACTCTGGTTTTCTG[G/T]CTTTCTCCGCAAGCC	114804
rs59025820	in-del	-/TC			intron-variant	RNF157	GRCh38.p7	17:76202129	CTCTCTCTCTCTCTC[-/TC]ACACACACACACACA	114804
rs59053255	snp	A/T	0.000399281	0.0141238	missense, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154306	GTGGGTGATCCATCC[A/T]CTTCCTCTATAACAT	114804
rs59153651	in-del	-/CAAATAAA	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76189838	GAGAACACAAACAAA[-/CAAATAAA]AACAACTGAAGGCTG	114804
rs59307532	snp	G/T	0.326506	0.238006	intron-variant	RNF157	GRCh38.p7	17:76200368	GATATACAGTGTATC[G/T]ATATAATGGCATATT	114804
rs59400912	in-del	-/AA			intron-variant	RNF157	GRCh38.p7	17:76220403	AAAAAAAAAAAAAAA[-/AA]GGTTACCTTTGAAGG	114804
rs59430937	in-del	-/T	0.424968	0.178567	intron-variant	RNF157	GRCh38.p7	17:76160375	TGCTGTTTTCTGCTG[-/T]TTTTTTTTTCAGTGC	114804
rs59479793	snp	C/T	0.0425829	0.139564	intron-variant	RNF157	GRCh38.p7	17:76172050	TCCCCTGGGTCAGGT[C/T]GGGGGACTGTTCTGC	114804
rs59560318	snp	A/G	0.0298908	0.118541	intron-variant	RNF157	GRCh38.p7	17:76176053	AGGAGAAGCTTGTTC[A/G]TGGGCTGCTACCCAC	114804
rs59610541	in-del	-/T			utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144339	TTTTTTTTTTTTTTT[-/T]CTCTGTCGCCCAGGC	114804
rs59629419	snp	C/G	0.0763149	0.179815	intron-variant	RNF157	GRCh38.p7	17:76193107	TACAGGCGTGGGCCA[C/G]AGCACTCAGCCTTCT	114804
rs59936899	snp	A/G	0.00835141	0.0640778	intron-variant	RNF157	GRCh38.p7	17:76210360	GCACTTTGGGAGGCC[A/G]AGGTGGGCGGATCAC	114804
rs59994016	snp	C/T	0.0948562	0.196037	intron-variant	RNF157	GRCh38.p7	17:76223581	ATTGATGATAAAATG[C/T]TTAACCATATAAAAC	114804
rs60128456	snp	A/G	0.00914312	0.0669923	intron-variant	RNF157	GRCh38.p7	17:76209783	TTGTTTTTTTGAGAC[A/G]GAGTCTCACTCTGTC	114804
rs60491535	in-del	-/AC			intron-variant	RNF157	GRCh38.p7	17:76202171	CACACACACACACAC[-/AC]GTGCATGAGAAAGAC	114804
rs60633196	snp	C/G/T	0.0652798	0.16874	intron-variant	RNF157	GRCh38.p7	17:76207137	AATTTGGCTTTGGGC[C/G/T]GGGCTTGGTGGCTCA	114804
rs60643972	snp	A/G	0.309894	0.242719	intron-variant	RNF157	GRCh38.p7	17:76181891	CCAGCCTGGGTGACC[A/G]AGTGAGACTCTGTCT	114804
rs60648252	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76233556	TTTATTTTTTTATTA[G/T]TGACAGGGTCTCAAT	114804
rs60689153	snp	C/T	0.328382	0.237395	intron-variant	RNF157	GRCh38.p7	17:76208421	TCTTTAAACTCTCTG[C/T]GCCACATGTTCTTCA	114804
rs60936294	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76210364	TTTGGGAGGCCAAGG[C/T]GGGCGGATCACGAGG	114804
rs60943338	snp	C/T	0.143622	0.226238	intron-variant	RNF157	GRCh38.p7	17:76208414	TGTGCAGTCTTTAAA[C/T]TCTCTGTGCCACATG	114804
rs61244689	snp	G/T	0.0611083	0.163768	intron-variant	RNF157	GRCh38.p7	17:76215111	ATAATACATTGAGGA[G/T]ATACACAAACTCCCT	114804
rs61741757	snp	C/G	0.0307617	0.120144	intron-variant	RNF157	GRCh38.p7	17:76226752	CCGACTGGTCGAAGG[C/G]GGACATCAAGTCCCC	114804
rs61741758	snp	A/G	0.0948562	0.196037	intron-variant	RNF157	GRCh38.p7	17:76226432	AGTCTCCTGGACTAG[A/G]GGGGCAAAGAGATTA	114804
rs61744818	snp	A/G	0.0380764	0.132621	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167678	TTCTGGAACTCTTCC[A/G]TGGCCTGGTAATAGA	114804
rs61745716	snp	A/C	0.0798611	0.183174	intron-variant	RNF157	GRCh38.p7	17:76202715	CAGCCTTGGCATAGT[A/C]CCAAAAAGTGGCCAA	114804
rs61751844	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151780	CAGCTCCAGGGAGCA[C/T]AGAGGAGCCCTAACT	114804
rs61751845	snp	A/G	0.0147141	0.0845029	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76158415	AGATGCTGAACCGAC[A/G]GTCTCTGAGAGAGCT	114804
rs61760884	snp	A/G	0.0116442	0.0754089	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF157	GRCh38.p7	17:76212385	TGGTCTGTTCCCCAG[A/G]AAGTTCAGATCGCTG	114804
rs61760885	snp	C/G/T	0.00692576	0.058482	missense, intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152363	CACTCACCAGGTAAG[C/G/T]AGACCTCAGAGCACA	114804
rs62086280	snp	A/G	0.494358	0.0528145	intron-variant	RNF157	GRCh38.p7	17:76227373	TGATCCGCCCACCTC[A/G]GCTTCCCAAACTGCT	114804
rs62090126	snp	C/G	0.0189856	0.0955633	utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142937	GTGGGAGAAGCCAGG[C/G]CCCACCTCTTCTCTT	114804
rs62090127	snp	A/G	0.5	0	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152719	AGTCAGATCACTGAG[A/G]AGGGCTGTGGGACAC	114804
rs62090128	snp	A/G	0.159202	0.232929	intron-variant	RNF157	GRCh38.p7	17:76162655	AAGGTTCAAGGACAG[A/G]CTGTCTCTACTGAGA	114804
rs62090129	snp	C/T	0.0766824	0.180169	intron-variant	RNF157	GRCh38.p7	17:76176884	GCACCTGGCCATTGG[C/T]GCAGCCACTGTGCCC	114804
rs62090130	snp	A/C/G	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76194782	GCACTTTGGGAGGCC[A/C/G]AGGTGGGCAGATCAC	114804
rs62090131	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76194786	TTTGGGAGGCCAAGG[C/T]GGGCAGATCACGAGG	114804
rs62090132	snp	A/G	0.00478085	0.0486577	intron-variant	RNF157	GRCh38.p7	17:76194791	GAGGCCAAGGTGGGC[A/G]GATCACGAGGTCAGG	114804
rs62090133	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76194798	AGGTGGGCAGATCAC[A/G]AGGTCAGGAGATCGA	114804
rs62090134	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76198505	TAGCTGGCTGCGTCC[G/T]TTGGGGGGCCTGAAC	114804
rs62090135	snp	C/T	0.0178098	0.0926698	intron-variant	RNF157	GRCh38.p7	17:76209792	TGAGACGGAGTCTCA[C/T]TCTGTCGCCCAGGCT	114804
rs62090136	snp	C/T	0.0178098	0.0926698	intron-variant	RNF157	GRCh38.p7	17:76211054	AGGTGATCTGTCCAC[C/T]TCGGCCTCCCAAAGT	114804
rs62090137	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76216384	AATGCCCTTTTATGC[C/T]ATAATATTAAAAGAA	114804
rs66472386	snp	C/T	0.229723	0.249176	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241213	ATAAGATCAAGACAT[C/T]CAGCCTCTGTCTGTA	114804
rs71161269	in-del	-/G	0	0	intron-variant	RNF157	GRCh38.p7	17:76171674	ATTAAGGTAACAGAA[-/G]GGAAAACACCTGGTG	114804
rs71161270	in-del	-/ATATATATATAT	0	0	intron-variant	RNF157	GRCh38.p7	17:76182788	ATATATATATCTCTC[-/ATATATATATAT]ATATATATATATATA	114804
rs71161271	in-del	-/AAAAAAAAAAAAAA	0	0	intron-variant	RNF157	GRCh38.p7	17:76185487	GCGAGACTCCGTCTC[-/AAAAAAAAAAAAAA]AAAAAAAAAAAAGAA	114804
rs71161273	in-del	-/AA	0	0	intron-variant	RNF157	GRCh38.p7	17:76190186	GTGAGAATCTATTTC[-/AA]AAAAAAAAAAAAAAA	114804
rs71161274	in-del	-/TTTTTTT	0	0	intron-variant	RNF157	GRCh38.p7	17:76210604	TTCTTTCTTTCTTTC[-/TTTTTTT]TTTTTTTTTTTTTTT	114804
rs71363617	in-del	-/G	0.5	0	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76148298	AGACAGGGTCTCTTG[-/G]CTCTGTCGCCCAGGC	114804
rs71363618	in-del	-/A	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76181925	AAAAAAAAAAAAAAA[-/A]GAATAAATAAATAAA	114804
rs71363619	in-del	-/A	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76191622	AAAAAAAAAAAAAAA[-/A]CATTAGCCAGGTGTA	114804
rs71363621	in-del	-/A	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76222033	GAGAGTGGGGACAAA[-/A]CTGCTTAATTGGTTT	114804
rs71382200	snp	C/T	0.174932	0.238463	intron-variant	RNF157	GRCh38.p7	17:76179657	GAGCTCATGCCACTG[C/T]ACTCCAGCCTGGGCA	114804
rs71704475	in-del	-/A/C			intron-variant	RNF157	GRCh38.p7	17:76197111	GGGTGGATCACCCAC[-/A/C]AGCCAGATGGCAATG	114804
rs71996459	in-del	-/AGG	0.111308	0.208002	intron-variant	RNF157	GRCh38.p7	17:76173809	TGTCAGAAACAAAGC[-/AGG]AGAAGGTGGTGTGTT	114804
rs72868709	snp	A/C			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151979	AAGGGCGCAGGCAAT[A/C]CTTCCAAGACCTTCG	114804
rs72868713	snp	C/T	0.00636936	0.0560724	intron-variant	RNF157	GRCh38.p7	17:76160137	AACATAAATATTTTC[C/T]TTTGTTTCTGAAGCC	114804
rs72868716	snp	C/T	0.125376	0.216727	intron-variant	RNF157	GRCh38.p7	17:76167166	GCAAAAGTCAGTATC[C/T]GGCACAGATGGGTCT	114804
rs72868721	snp	C/T	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76181037	TACAGATAAAGAAAC[C/T]GAGACTCAAAAGATT	114804
rs72868723	snp	G/T	0.327914	0.237549	intron-variant	RNF157	GRCh38.p7	17:76191718	GGTTGAAACTACAAT[G/T]AGCTATAATTGCACC	114804
rs72868724	snp	G/T	0.127944	0.218179	intron-variant	RNF157	GRCh38.p7	17:76198509	TGGCTGCGTCCTTTG[G/T]GGGGCCTGAACATAC	114804
rs72868727	snp	A/G	0.184838	0.241358	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212772	GAAGCTGAGGCAGGA[A/G]GATGGCTTGAACCCA	114804
rs72868733	snp	A/G	0.248188	0.249993	intron-variant	RNF157	GRCh38.p7	17:76215979	GAGGGGAGGTACCTA[A/G]TTGCCTTAAGTAGAA	114804
rs72868739	snp	C/T	0.248755	0.249997	intron-variant	RNF157	GRCh38.p7	17:76231058	ATCCTCTTGTTTGTG[C/T]CTTCTGAGTAGCTGG	114804
rs72868740	snp	A/G	0.25912	0.249834	intron-variant	RNF157	GRCh38.p7	17:76232191	AGTTCGAGACCAGCC[A/G]GGGCAACGTAGTGGG	114804
rs72868742	snp	G/T	0.25912	0.249834	intron-variant	RNF157	GRCh38.p7	17:76232200	CCAGCCAGGGCAACG[G/T]AGTGGGACCCCGTCT	114804
rs73345573	snp	G/T	0.0107246	0.0724382	utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76143119	AGAAGGCAGGGGGAG[G/T]GAGGAAGAGGAGAAA	114804
rs73345576	snp	G/T	0.0107246	0.0724382	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76143545	TGTAGGGGGAAGGAA[G/T]GAAAGAACATTAGGT	114804
rs73345581	snp	C/G	0.030278	0.119257	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149194	AGTGCCTCTAAGCCC[C/G]TCACCAGTGTTATCA	114804
rs73345584	snp	A/G	0.00914312	0.0669923	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149460	ATGAGGCGCCAAGAC[A/G]GCCAGTGGTATCTCA	114804
rs73345586	snp	C/T	0.0189856	0.0955633	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152598	AAGACAATAATTAAG[C/T]GGATAAAGAGTGGAC	114804
rs73345592	snp	C/G	0.00676609	0.0577691	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76155144	ATGTCCCCTAGGAAG[C/G]CTTCGTCAGCGCAGC	114804
rs73345593	snp	A/C	0.00218203	0.0329584	intron-variant, synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76155315	AGACTCCGCTGGCAG[A/C]CCCTGCAGAAGAGCA	114804
rs73345600	snp	A/C	0.0592355	0.161582	intron-variant	RNF157	GRCh38.p7	17:76159060	GAAGGCCCTATCCAC[A/C]GTGTTCAACATCCTC	114804
rs73345601	snp	C/T	0.0592355	0.161582	intron-variant	RNF157	GRCh38.p7	17:76159179	CATCTTATTTTCATC[C/T]CTTAATGGATGGGAT	114804
rs73347503	snp	C/T	0.0248432	0.108648	intron-variant	RNF157	GRCh38.p7	17:76160315	TATTAAATTATTAGC[C/T]CTTAGATGATGAGGT	114804
rs73347513	snp	A/G	0.0425829	0.139564	intron-variant	RNF157	GRCh38.p7	17:76168463	GTTGCGTAGTTTCCT[A/G]TGTACTCATCACAAA	114804
rs73358694	snp	C/G	0.00676609	0.0577691	intron-variant	RNF157	GRCh38.p7	17:76172039	GCTGGATGAACTCCC[C/G]TGGGTCAGGTCGGGG	114804
rs73360605	snp	C/T	0.0437281	0.141251	intron-variant	RNF157	GRCh38.p7	17:76182546	ATTACACTACTCCTA[C/T]GGTTGTACTATTTTT	114804
rs73360613	snp	C/T	0.00914312	0.0669923	intron-variant	RNF157	GRCh38.p7	17:76188589	GTGCAATAGATGCAA[C/T]AGATAATTCCCCCCA	114804
rs73360615	snp	A/G	0.0577344	0.159793	intron-variant	RNF157	GRCh38.p7	17:76193010	ACTTTTTGTAGAGAC[A/G]GGACCTCGCTGTTTC	114804
rs73360619	snp	A/C	0.0726307	0.176182	intron-variant	RNF157	GRCh38.p7	17:76195613	TAGCCAAAATGCCCC[A/C]AAAAAGCTCAATGCC	114804
rs73360621	snp	A/G	0.259951	0.249802	intron-variant	RNF157	GRCh38.p7	17:76196038	TGCACATAATTAAAA[A/G]TGGGTATAAATATGA	114804
rs73360623	snp	A/G	0.0562307	0.157967	intron-variant	RNF157	GRCh38.p7	17:76196309	CAGTTCCACTTATAT[A/G]AAGTTCAAACCAGGA	114804
rs73360624	snp	C/G	0.205417	0.245993	intron-variant	RNF157	GRCh38.p7	17:76196746	AACTGGGAACCAGAG[C/G]CACCTGATCCAAGAG	114804
rs73360627	snp	A/G	0.0707826	0.174302	intron-variant	RNF157	GRCh38.p7	17:76199054	AACATCAGCCTGGAG[A/G]ACAATGGGTATTCCA	114804
rs73360638	snp	A/C	0.078151	0.181571	intron-variant	RNF157	GRCh38.p7	17:76201885	ATTTTGCACTACTAC[A/C]AGTAATGCTACAATA	114804
rs73360640	snp	C/T	0.0648419	0.167978	intron-variant	RNF157	GRCh38.p7	17:76202305	TCTCCAAACATAACA[C/T]GTGCACAGCATCTGG	114804
rs73360641	snp	A/G	0.077417	0.180873	intron-variant	RNF157	GRCh38.p7	17:76202388	ACTCACACTGCTGCA[A/G]TTCTCTAATCTGCAC	114804
rs73360646	snp	A/C	0.215747	0.247642	intron-variant	RNF157	GRCh38.p7	17:76204632	ATGGATATACTACCA[A/C]GTTCCTTTAAATAAC	114804
rs73360649	snp	A/G	0.067446	0.170804	intron-variant	RNF157	GRCh38.p7	17:76205703	GCACTCTAGCCTGGC[A/G]ACGGAGCAAGACTCC	114804
rs73362568	snp	C/G	0.0248432	0.108648	intron-variant	RNF157	GRCh38.p7	17:76206014	ACAGGAAGACTACTT[C/G]AGCAAAGGAGTTTGA	114804
rs73362571	snp	A/G	0.211516	0.24702	intron-variant	RNF157	GRCh38.p7	17:76206164	TAAGCCTAGGAAGTC[A/G]AGGCTGCAGTGAGCT	114804
rs73362572	snp	A/C	0.0659589	0.169201	intron-variant	RNF157	GRCh38.p7	17:76208081	CCACCACGCCTGGCT[A/C]ATTTTTATCATTTTA	114804
rs73362574	snp	A/T	0.0588605	0.161139	intron-variant	RNF157	GRCh38.p7	17:76209658	AGGCCAAAATTTTTT[A/T]AAAAATATATAAACT	114804
rs73362597	snp	C/T	0.0490535	0.14873	intron-variant	RNF157	GRCh38.p7	17:76221008	GGGCCTTGGTCCTAG[C/T]TATTCAGGAGGCTGA	114804
rs73364508	snp	C/T	0.0607341	0.163335	intron-variant	RNF157	GRCh38.p7	17:76228466	TCTCATTCCCAACTG[C/T]CTCTACCTCACCTGA	114804
rs73364509	snp	A/G	0.0391387	0.134304	intron-variant	RNF157	GRCh38.p7	17:76230474	GTTCAATTACAATGG[A/G]TTATCTTCTAAGAGT	114804
rs73364511	snp	C/G	0.0283406	0.115616	intron-variant	RNF157	GRCh38.p7	17:76231583	GATTGCTTGAGCCCA[C/G]GAGTAGAAGATCAGC	114804
rs73364512	snp	C/T	0.0333695	0.124785	intron-variant	RNF157	GRCh38.p7	17:76232547	TATTATGAGCAATGC[C/T]GCTATGAACATCTGC	114804
rs73364513	snp	C/G	0.0174175	0.0916809	intron-variant	RNF157	GRCh38.p7	17:76232844	ATATTTCCCTAATGG[C/G]TGCTGATGTTGAGTA	114804
rs73364515	snp	C/T	0.0611083	0.163768	intron-variant	RNF157	GRCh38.p7	17:76234776	TTCTTGTCATACCTA[C/T]GATTTATAAAAATTT	114804
rs73996148	snp	A/C	0.0349115	0.127424	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144292	AAGGGAAATCATCTT[A/C]ACTGGGGGATTCTCA	114804
rs73996149	snp	A/C	0.0689305	0.172377	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145491	ATGACGGTGCGAGCC[A/C]CAGCACTCGTGTGTG	114804
rs73996150	snp	C/T	0.0287284	0.116357	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149420	GTGCAGCTGTTCTGA[C/T]GGGAGAGAGCTGGCC	114804
rs73996169	snp	A/G	0.0298908	0.118541	intron-variant	RNF157	GRCh38.p7	17:76191993	TCAGTAACAGTTAAG[A/G]CCACTATGCATCTCT	114804
rs73996170	snp	A/G	0.0287284	0.116357	intron-variant	RNF157	GRCh38.p7	17:76193651	ACTGTCTAAGGTAAC[A/G]TGAGAGTTAAGCACG	114804
rs73996177	snp	C/G	0.0345262	0.126772	intron-variant	RNF157	GRCh38.p7	17:76198480	CTGCACATAAAGTGG[C/G]AAAATCCACTAGCTG	114804
rs73996179	snp	C/T	0.205417	0.245993	intron-variant	RNF157	GRCh38.p7	17:76198700	AATCTACCTTCTACA[C/T]TTCATCTGAGAGATC	114804
rs73996189	snp	A/G	0.0952156	0.196321	intron-variant	RNF157	GRCh38.p7	17:76221509	AGAATATATTGTAAG[A/G]GGGGAAAGTATGGCA	114804
rs73996195	snp	A/G	0.0150606	0.0854603	intron-variant	RNF157	GRCh38.p7	17:76238451	GATTATTTATTGAGT[A/G]TGCTAATTAACAAAA	114804
rs74329025	snp	C/T	0.00393126	0.0441608	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76167779	CTCTTCTCCAGGGCT[C/T]TTCACTTCCTCAGCA	114804
rs74353882	snp	C/T	0.000479922	0.0154832	intron-variant	RNF157	GRCh38.p7	17:76158505	TGGGAAGTGGATCTG[C/T]AGGAGTCCAGTGGAA	114804
rs74481814	snp	A/C	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76190602	AGTGAGACCCCATCT[A/C]AAAAAAAAAAAAAAA	114804
rs74504867	snp	A/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76156618	GTCACCCTGCAGCTG[A/T]GACATGGGGACACCC	114804
rs74553430	snp	A/G	0.118584	0.212673	intron-variant	RNF157	GRCh38.p7	17:76211379	CCTGCCCTTGCCATT[A/G]TCTTCTCCCACTCTC	114804
rs74554341	snp	C/T	0.0217236	0.101931	intron-variant	RNF157	GRCh38.p7	17:76163168	CAACATGCAGCAAAA[C/T]TACACCTCTTGGCCC	114804
rs74560220	snp	C/G	0.040671	0.13668	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147697	CCCTGCTGCTGCTCC[C/G]TCCTCAGCCTCATTC	114804
rs74560598	snp	A/G	0.0130921	0.0798413	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152655	TGTCTGTGTTCTCGC[A/G]CTTTCCTGCTGTTTC	114804
rs74593550	snp	A/G	0.029116	0.117091	intron-variant	RNF157	GRCh38.p7	17:76171880	CAGCCAGGCTGCCAC[A/G]GCAGAGGCTATGACC	114804
rs74597166	snp	C/G	0.00835141	0.0640778	intron-variant	RNF157	GRCh38.p7	17:76222640	CATTTTTCAGTTGAG[C/G]AAACTAAGGATTAGA	114804
rs74601024	snp	A/T	0.029116	0.117091	intron-variant	RNF157	GRCh38.p7	17:76176511	TTTCTTAGTGAGTTA[A/T]CTTCCTTTCAAAAAT	114804
rs74703313	snp	C/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76155034	CTCCACACCAGTGAC[C/T]CTGGGAACCAGTGGC	114804
rs74723988	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76219562	AGGGACCAGACAGAA[A/G]GTAGATTTCTTTGAA	114804
rs74755440	snp	A/G	0.0134861	0.0810011	intron-variant	RNF157	GRCh38.p7	17:76218067	ATGATTAAATTTAAC[A/G]TTATGTGTTTTTTTG	114804
rs74854106	snp	A/C	0.17461	0.238362	intron-variant	RNF157	GRCh38.p7	17:76185728	CCCGCCTCGGCCTCC[A/C]AAAGTGCTGGGATTA	114804
rs75101071	snp	A/G	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76180397	TCTATTCATCTAACC[A/G]GAAAACTCTGCCAAA	114804
rs75120746	snp	A/G	0.0418186	0.138422	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153230	TTCTATGGGAGAAAC[A/G]ATCACAAGGGGTAAC	114804
rs75202027	snp	G/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76228573	TACAAGCATATACTG[G/T]TCTCCCCAACTCAAA	114804
rs75465497	snp	C/T	0.0948562	0.196037	intron-variant	RNF157	GRCh38.p7	17:76235489	AGGCGTGAGCCACTG[C/T]GCCCAGCCGTAAATT	114804
rs75481553	snp	C/T	0.0170251	0.090679	intron-variant	RNF157	GRCh38.p7	17:76179864	CATGCACCAGTCCAC[C/T]GTACTTAGCATTAGC	114804
rs75522588	snp	A/T	0.00318978	0.0398085	intron-variant	RNF157	GRCh38.p7	17:76210134	CTCTATCAGAAAAAA[A/T]GAAAGATCTGTCTAC	114804
rs75524217	snp	C/T			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213119	ATTAATGATCATATA[C/T]ATTTTTTGGTTCCTG	114804
rs75534064	snp	C/T	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76184337	CTACATAATCTCTTT[C/T]TTTATAGGGTTTTGT	114804
rs75617218	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76171006	CACATCATTCTCCTG[A/C]CTCAGCCTCCCAAAT	114804
rs75625050	snp	A/T			utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144360	TCGCCCAGGCTGGAG[A/T]GCATTGGCGCGATCT	114804
rs75633162	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76143521	TAACTATGAAAGGGG[C/T]GGGAAGAATGTAGGG	114804
rs75721603	snp	A/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76202639	TATTAGAGCGCTACT[A/T]TTTTTTTTTTCAGGC	114804
rs75783473	snp	C/T	0.0517044	0.152246	intron-variant	RNF157	GRCh38.p7	17:76231570	CCCAAAGTGGAAGGA[C/T]TGCTTGAGCCCAGGA	114804
rs75786326	snp	C/T	0.0205511	0.0992634	intron-variant	RNF157	GRCh38.p7	17:76188056	TTCTTCAGTCACCCC[C/T]CAATAGCAGTGGGCA	114804
rs75894850	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76171004	TTCACATCATTCTCC[A/T]GCCTCAGCCTCCCAA	114804
rs75941231	snp	C/T	0.0142736	0.0832652	intron-variant	RNF157	GRCh38.p7	17:76229623	CTCAAACTCAATAAC[C/T]TTTTCTTCTGGAAGG	114804
rs76027598	snp	G/T	0.029116	0.117091	intron-variant	RNF157	GRCh38.p7	17:76176323	GGCTTCATGGAGGAG[G/T]TGGTAGTTGATCTGG	114804
rs76090105	snp	A/C	0.00995522	0.0698463	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154377	AGCGGCAAAATGAGT[A/C]AACTGATTGGCTGAA	114804
rs76169669	snp	C/T	0.0221141	0.102801	intron-variant	RNF157	GRCh38.p7	17:76168619	CACCTGGCTCCCAGT[C/T]GCCACCCTGGAATCT	114804
rs76220936	snp	A/G	0.0158469	0.0875917	intron-variant	RNF157	GRCh38.p7	17:76194722	AGAGAAAAATATAAA[A/G]CCACAAGAGCAGGCC	114804
rs76242386	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76236638	TCACACAATTATTAA[G/T]AAATCTAAAAATCAC	114804
rs76252033	snp	A/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76215555	TAAAAAAAAAAAAAA[A/T]ATGAGATTCAGTACT	114804
rs76318926	snp	A/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76208990	AAAAAAAAAAAAAAT[A/T]CATTTGCTATGTGTA	114804
rs76348080	snp	A/G	0.00438332	0.0466095	intron-variant	RNF157	GRCh38.p7	17:76180672	TCAAGTGATCTTCTC[A/G]CCTCAGCTTCCCAAA	114804
rs76469028	snp	A/G	0.0364509	0.129988	intron-variant	RNF157	GRCh38.p7	17:76160764	GGTGGTAAAATGTAT[A/G]GTTCTTGCTTTCAAG	114804
rs76518642	snp	A/T	0.00755907	0.0610114	intron-variant	RNF157	GRCh38.p7	17:76193824	CAGTGAGGCTGCCGC[A/T]CCCATAGTTTCAGAT	114804
rs76596061	snp	A/C	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76220957	AGTGAGATGCTGTCT[A/C]AAAAAAAAAAAAAAA	114804
rs76669035	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150317	TAATCTCTAAATAGC[C/T]GGCTCCACAAGTCAC	114804
rs76763466	snp	C/T	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76173862	CCTCGCTTTACAGTT[C/T]GCCAAGAATAGCCCT	114804
rs76822643	snp	A/G	0.0314385	0.121371	intron-variant	RNF157	GRCh38.p7	17:76237554	CATAATCATGGAATG[A/G]TTGTTTTAAGTCTTG	114804
rs76892977	snp	C/G	0.0217236	0.101931	intron-variant	RNF157	GRCh38.p7	17:76220334	TATTAAGCTTCATCA[C/G]GATAATAAGGGCAAG	114804
rs76915053	snp	A/G	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76174029	TCTTCTTTTTCCATT[A/G]TATGAAGCTTATTTC	114804
rs77001045	snp	A/G	0.067446	0.170804	intron-variant	RNF157	GRCh38.p7	17:76185184	CACACCTACATGGCT[A/G]CGTGAACTGCTTAGA	114804
rs77059531	snp	A/C	0.0232847	0.105357	intron-variant	RNF157	GRCh38.p7	17:76192940	GGCTCAAGTGATTCT[A/C]CCACTTCAGCCACGT	114804
rs77107809	snp	A/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76208988	CAAAAAAAAAAAAAA[A/T]TTCATTTGCTATGTG	114804
rs77119800	snp	A/T	0.00676609	0.0577691	intron-variant	RNF157	GRCh38.p7	17:76230396	TCAGTCATCAAAGAA[A/T]CAAAAACACTGAACA	114804
rs77137584	snp	A/T	0.0170251	0.090679	intron-variant	RNF157	GRCh38.p7	17:76175161	GTTTCTTTTTCACCT[A/T]AAAAGATGTGGTAAA	114804
rs77170514	snp	A/C	0	0	intron-variant	RNF157	GRCh38.p7	17:76163392	TAGAGACGGGGTTTC[A/C]CCGTGTTAGCCAGGA	114804
rs77188968	snp	C/G/T	0.00796298	0.0626859	intron-variant	RNF157	GRCh38.p7	17:76157304	GGCTACTGAAACCCT[C/G/T]TCCTGGCTGGGTCTG	114804
rs77310609	snp	C/T	0.0103295	0.0711199	intron-variant	RNF157	GRCh38.p7	17:76222767	AACCCTGCACCTGTC[C/T]CTCCATCTGACAGTG	114804
rs77315634	snp	G/T	0.0205511	0.0992634	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144764	GGAAACGCTACGTCC[G/T]TGCAGTATGGCTCTC	114804
rs77318707	snp	A/C	0.029116	0.117091	intron-variant	RNF157	GRCh38.p7	17:76175513	AATTCTAGTTCAGAT[A/C]CCATCTGTGGCCTGT	114804
rs77320699	snp	G/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76227116	AATAACCTCTTTTTT[G/T]GTTTTTTTTTTTTTT	114804
rs77390005	snp	C/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76190298	CAGCCTCCTGAATAG[C/T]TAGGTCCACAGGCAC	114804
rs77418551	snp	A/G			missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159399	GGCGGTCAAGAGGCG[A/G]GATCGTCCTGACGGG	114804
rs77514428	snp	C/T	0.0205511	0.0992634	intron-variant	RNF157	GRCh38.p7	17:76185020	ACGAAAAACCTACCA[C/T]AGAGTAAAGAACACA	114804
rs77518962	snp	C/T	0	0	intron-variant	RNF157	GRCh38.p7	17:76163410	GTCAGGAGATCGAGA[C/T]CATCCTGGCTAACAA	114804
rs77551906	snp	A/G	0.0221141	0.102801	intron-variant	RNF157	GRCh38.p7	17:76207158	TGGTGGCTCACACCT[A/G]CAATCCCAACACTTT	114804
rs77637475	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76236636	ATTCACACAATTATT[A/G]ATAAATCTAAAAATC	114804
rs77751164	snp	G/T	0.0872718	0.189788	intron-variant	RNF157	GRCh38.p7	17:76207569	GAAGTCTATGGCATT[G/T]ATAGCTTAATATAAC	114804
rs77762154	snp	A/G	0.0263992	0.111815	intron-variant	RNF157	GRCh38.p7	17:76201410	CCAGCTACCAGGAAG[A/G]CTGAGGCAGGAGGAC	114804
rs77851196	snp	A/G	0.0221141	0.102801	intron-variant	RNF157	GRCh38.p7	17:76192285	TTAGTGGCACTTTTC[A/G]AGTCAGCAACATTTA	114804
rs77960453	snp	A/T	0.0162398	0.0886349	intron-variant	RNF157	GRCh38.p7	17:76207265	TCTCTACAAAAAAAA[A/T]TTTAAAAATTAGCCC	114804
rs78269275	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76171005	TCACATCATTCTCCT[C/G]CCTCAGCCTCCCAAA	114804
rs78308836	snp	A/G	0.202035	0.245356	intron-variant	RNF157	GRCh38.p7	17:76192971	GAGTAACAGCCGCGC[A/G]CCACCACACCTAGCT	114804
rs78384939	snp	A/G	0.0107246	0.0724382	intron-variant	RNF157	GRCh38.p7	17:76174126	GGACACACTGTGGCC[A/G]AGTTAATCACAAAAG	114804
rs78399909	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76143487	CAGGAAGTGGGGTTA[C/T]TGCTCAGCTTATGCA	114804
rs78431454	snp	A/G	0.0329836	0.124112	intron-variant	RNF157	GRCh38.p7	17:76198508	CTGGCTGCGTCCTTT[A/G]GGGGGCCTGAACATA	114804
rs78434886	snp	A/G	0.0142736	0.0832652	intron-variant	RNF157	GRCh38.p7	17:76230272	GGATCTTGAGGCAAA[A/G]TAAAGCAACCAGCCG	114804
rs78438390	snp	C/T	0.0295035	0.117819	intron-variant	RNF157	GRCh38.p7	17:76232596	ACATATGTTTTCATT[C/T]TTTTGGACAGATTCA	114804
rs78484150	snp	C/T	0.0170251	0.090679	intron-variant	RNF157	GRCh38.p7	17:76188739	GGCTCCATAATTAAG[C/T]GGGAAGTCAAAAGTT	114804
rs78485105	snp	C/T	0.00438332	0.0466095	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154036	AAATATGGACCTGTA[C/T]GTATCTCCTGCAGCA	114804
rs78520644	snp	A/C	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76181911	AGACTCTGTCTCAAA[A/C]AAAAAAAAAAAAAAG	114804
rs78532161	snp	C/T	0.0142736	0.0832652	intron-variant	RNF157	GRCh38.p7	17:76214655	ACATACCCTCTCCAC[C/T]TCAAATTCATTAACA	114804
rs78584827	snp	C/G	0.375	0.216506	intron-variant	RNF157	GRCh38.p7	17:76233273	TATTGAGTTGTAAGA[C/G]TTCTTAATATTGATA	114804
rs78665503	snp	C/T	0.0298908	0.118541	intron-variant	RNF157	GRCh38.p7	17:76179042	TCAGATAAATGTTTG[C/T]GTTTGTCCACACTAT	114804
rs78730150	snp	C/T	0.0130921	0.0798413	intron-variant	RNF157	GRCh38.p7	17:76209446	GGCCCAACAGAAACT[C/T]GTAAACTTTCTTAAA	114804
rs78760030	snp	C/T	0.0221141	0.102801	intron-variant	RNF157	GRCh38.p7	17:76192026	AAATGCTGAAAAAGT[C/T]AACCAGATTTTTCTT	114804
rs78785076	snp	C/T	0.0952156	0.196321	intron-variant	RNF157	GRCh38.p7	17:76232808	ATAGGTGTGAAATGG[C/T]ATCTCATTGCAGTTT	114804
rs78856872	snp	C/T	0.0209421	0.100162	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76148245	TTTCCACTAAAAAGA[C/T]CCAAATTATCTTTGC	114804
rs78861432	snp	A/C	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76222346	AGCAAGACCCCGTCT[A/C]AAAAAAAAAAAAAAA	114804
rs78916891	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76229815	ACTGCTTGTAATTTG[C/T]TTTTCTTCTAAGATA	114804
rs78960400	snp	A/C	0	0	intron-variant	RNF157	GRCh38.p7	17:76191621	AAAAAAAAAAAAAAA[A/C]ACATTAGCCAGGTGT	114804
rs78987044	snp	G/T	0.0142736	0.0832652	intron-variant	RNF157	GRCh38.p7	17:76234261	TGCAGACTTACCATA[G/T]TTTATTTATCAGTAG	114804
rs79015157	snp	A/G	0.00473695	0.0484359	intron-variant	RNF157	GRCh38.p7	17:76155523	GGACATGTGCACAAA[A/G]AACAGAGAAGCCAGG	114804
rs79222481	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76158115	TATTGTCTTTTGTGC[A/C]CCCCACCCCAGATAG	114804
rs79230936	snp	A/G	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76173572	CCCGCACTCCTGTCT[A/G]AGGCCCAGAGAAGCA	114804
rs79252974	snp	A/C			missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76158409	TCTCCGAGATGCTGA[A/C]CCGACGGTCTCTGAG	114804
rs79284497	snp	A/C	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76179698	CTCTGTCTCAAAAAC[A/C]AAAAATAAGTATCTT	114804
rs79290419	snp	A/C	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76222348	CAAGACCCCGTCTCA[A/C]AAAAAAAAAAAAAAA	114804
rs79292458	snp	C/T	0.0221141	0.102801	intron-variant	RNF157	GRCh38.p7	17:76168017	ACACCATTGTGCATT[C/T]GGCACTTTTGTTTTT	114804
rs79293525	snp	G/T	0.029116	0.117091	intron-variant	RNF157	GRCh38.p7	17:76216723	AATTAGACCCTTGTC[G/T]CGACAAAAAATTAAA	114804
rs79338325	snp	A/G	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76238418	CAGTTAAACTTTTAA[A/G]ACTGGTAGAGAGGAG	114804
rs79349524	snp	C/T	0.0107246	0.0724382	intron-variant	RNF157	GRCh38.p7	17:76200970	ACACTTCCTGGCACA[C/T]ATCCCAACCCCAGCG	114804
rs79349605	snp	G/T	0.0633504	0.166319	intron-variant	RNF157	GRCh38.p7	17:76224444	GAATCCTAGTAAATT[G/T]TCATATATTTGAAAA	114804
rs79397055	snp	A/G	0.0142736	0.0832652	intron-variant	RNF157	GRCh38.p7	17:76235031	CTCTTCATTGTGCCA[A/G]TACCACACTATCTTG	114804
rs79398395	snp	C/T	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76165382	AACCTCTTTCACCAT[C/T]ATAGCCTCTAAAGCC	114804
rs79453882	snp	A/G	0.5	0	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150137	CATATAGTCTCACAC[A/G]TATTTTTTTTCTTGG	114804
rs79477452	snp	C/T	0.00318978	0.0398085	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149862	AACATGGTAAAACTC[C/T]GTCTCTGCTAAAAAT	114804
rs79483022	snp	A/G	0.0123036	0.0774623	intron-variant	RNF157	GRCh38.p7	17:76194450	GGCGGTAAATTCACT[A/G]GAGCCTGAGATGACT	114804
rs79583534	snp	C/T	0.0433465	0.140692	intron-variant	RNF157	GRCh38.p7	17:76198688	TCATGACTCTCTAAT[C/T]TACCTTCTACACTTC	114804
rs79622987	snp	A/C	0.5	0	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150042	TGTCTCAAAAAAAAC[A/C]AAAAACAAAAACAAA	114804
rs79666138	snp	A/G	0.0221141	0.102801	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153866	AAGACCTGACCAGCT[A/G]CCAAATAGTCCTCCC	114804
rs79676884	snp	A/T	0.0119091	0.0762411	intron-variant	RNF157	GRCh38.p7	17:76223516	CATAAACAATACCTG[A/T]CTCTTCCTTTTCCTG	114804
rs79746102	snp	A/C	0.0295035	0.117819	intron-variant	RNF157	GRCh38.p7	17:76233569	TAGTGACAGGGTCTC[A/C]ATCTGTCACCCAGGC	114804
rs79842518	snp	A/C	0.0244538	0.107838	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151643	CGGGCACACTAACTA[A/C]AAAGGCACTCGGTGC	114804
rs79843807	snp	A/G	0.00557542	0.0525036	intron-variant	RNF157	GRCh38.p7	17:76178964	AGGATTAAAGTGCTG[A/G]TTATTAAAAGATCTG	114804
rs79855516	in-del	-/AA			intron-variant	RNF157	GRCh38.p7	17:76191039	AAAAGAAAAAAAAAA[-/AA]GTTACGATATGGATT	114804
rs79860525	snp	A/G	0.0130921	0.0798413	intron-variant	RNF157	GRCh38.p7	17:76231749	AAACCCCTCTGTGCT[A/G]TTATTTTTAAGAGCT	114804
rs79929195	snp	A/C	0.00755974	0.0610141	intron-variant	RNF157	GRCh38.p7	17:76166559	GGAAAGGAAAAAAAA[A/C]GAGGACTTAACACAT	114804
rs79942242	snp	C/T	0.375	0.216506	intron-variant	RNF157	GRCh38.p7	17:76232265	AAGTAGCTAGGACTA[C/T]AGGTGCTCGATGCCT	114804
rs79962229	snp	C/T	0.0142736	0.0832652	intron-variant	RNF157	GRCh38.p7	17:76216697	CATTAAAAATGTTCA[C/T]AATATATTATAATTA	114804
rs80000816	snp	A/G	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76199590	AAAAAAAAAAAAAAA[A/G]AAGAACAGCTGGCAG	114804
rs80021847	snp	A/T	0.030278	0.119257	intron-variant	RNF157	GRCh38.p7	17:76209651	ACTGAAAAGGCCAAA[A/T]TTTTTTTAAAAATAT	114804
rs80048320	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76161119	AGGAAACTGAAGTCA[C/G]TTACTTTATCTCAGG	114804
rs80054570	snp	A/G	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76214328	TTTTCTGTGCTGCTT[A/G]TGTTGTGAGTGTATA	114804
rs80058135	snp	C/T	0.0150606	0.0854603	intron-variant	RNF157	GRCh38.p7	17:76164345	TCTAATTACACTAAA[C/T]TGGACCCTAATGCTT	114804
rs80141857	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76236637	TTCACACAATTATTA[A/G]TAAATCTAAAAATCA	114804
rs80158254	snp	A/C	0.00478085	0.0486577	intron-variant	RNF157	GRCh38.p7	17:76235076	ATAGTAATTATATGC[A/C]TAGTAACTTTTAAAA	114804
rs80191105	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76182742	GTTTTCATTTGCTAT[A/T]AGATTCAGGCCTCGT	114804
rs80220380	snp	C/T	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76188145	CATTTAAAGACCGGA[C/T]ATAGTGAAATGCAGT	114804
rs80224057	snp	C/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76187198	TTCTTCTTTTTTTTT[C/T]CTTAAGATGGAGTCT	114804
rs80260056	snp	A/C	0.0225045	0.103662	intron-variant	RNF157	GRCh38.p7	17:76194149	TGACAAACACACACA[A/C]CAGTGTAACCACCAT	114804
rs80272219	snp	C/G	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76175371	AGAAGTGGAATTACA[C/G]GATCAAAGAGTAAGC	114804
rs80297761	snp	C/T	0.0228947	0.104514	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147967	AATTTCACAAGCCCC[C/T]TTCCTGCCTCTACAA	114804
rs80327383	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76176596	CGCTGCCATCACAAC[A/G]GCTGCTGCAGGGGGG	114804
rs80345918	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76168032	TGGCACTTTTGTTTT[C/T]ATTTTAATAAAAGTT	114804
rs111232540	snp	C/T	0.00318978	0.0398085	intron-variant	RNF157	GRCh38.p7	17:76167494	AAAAAGAATGTTTTC[C/T]GCCCTTGCTGAGTGG	114804
rs111239013	snp	A/G	0.0391387	0.134304	intron-variant	RNF157	GRCh38.p7	17:76179169	GAGGCTGAGGCAGAA[A/G]GATCGCTTGAGCTTA	114804
rs111240771	snp	A/G	0.0174175	0.0916809	intron-variant	RNF157	GRCh38.p7	17:76200237	ACAGAGCGGGACTCC[A/G]TCTTGTCAAAAAAAA	114804
rs111250983	snp	A/G	0.248188	0.249993	intron-variant	RNF157	GRCh38.p7	17:76235389	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	114804
rs111286512	snp	A/G	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76164541	TCAGCATTCCTTTCA[A/G]GCCACCCAAGTCGTT	114804
rs111291398	snp	A/G	0.00795532	0.062565	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153956	CTGTGGGGCTCCACT[A/G]AAAACCTGCAGCAGG	114804
rs111326194	snp	C/T	0.0010881	0.0232995	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159411	GCGAGATCGTCCTGA[C/T]GGGGGGCAGGTGGCC	114804
rs111377639	snp	C/T	0.5	0	upstream-variant-2KB	RNF157	GRCh38.p7	17:76240771	GCCGGAGCTGGGACC[C/T]CAGGAGACGAGCGCT	114804
rs111434625	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76178309	TCCCTGGTGCCAACC[A/G]GGAGAGCTGCTTGCA	114804
rs111436096	snp	C/T	0.0244538	0.107838	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145104	GAGGGATTGTGGTTA[C/T]AGGTTGTAACAGCTG	114804
rs111449764	snp	C/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76166904	GCTGAAAGGTAAGCA[C/T]GGCCTTCAAGCATCC	114804
rs111547576	snp	C/T	0.0618563	0.164627	intron-variant	RNF157	GRCh38.p7	17:76222994	CTCCTGGGTTCACGC[C/T]GTTCTCCTGCCTCAG	114804
rs111553491	in-del	-/A	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76212063	TTAAGTGCCATGAAG[-/A]AAAAAAAAAAAAGGT	114804
rs111589608	snp	C/T	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76174862	TAGAAATTATCTTCA[C/T]TCAGATTACTCACTT	114804
rs111601073	snp	A/G	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76187223	GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC	114804
rs111651709	snp	A/C	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76187760	CACCACATCCAGCTA[A/C]TTTGTTTTGTAATTT	114804
rs111674841	snp	A/G	0	0	intron-variant	RNF157	GRCh38.p7	17:76157520	AAATGCTATTCCTCC[A/G]TAACACATTTTCTGA	114804
rs111702630	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76227004	CCCTAATATGCCATG[A/G]TGGCCGTGGACCCTG	114804
rs111707425	snp	C/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76216847	AGTGAGCCATGACTG[C/T]GCCATTACATTCCAG	114804
rs111713374	snp	G/T	0.0142736	0.0832652	intron-variant	RNF157	GRCh38.p7	17:76236550	AACCGTGCTCTAAAT[G/T]GCTTTCTATGCTAAT	114804
rs111750592	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76236658	CTAAAAATCACCTAA[C/T]GCATAACATTATTCA	114804
rs111757190	snp	C/T	0.0356815	0.128715	intron-variant	RNF157	GRCh38.p7	17:76169428	TGTTTCCAATTAGAT[C/T]TTTTTTACTTTATTA	114804
rs111758174	snp	C/T	0.0252325	0.109451	intron-variant	RNF157	GRCh38.p7	17:76181536	GGATACGTCAGTCAG[C/T]GTTTACCTTCCACCC	114804
rs111802242	snp	G/T	0.0244538	0.107838	intron-variant	RNF157	GRCh38.p7	17:76174039	CCATTATATGAAGCT[G/T]ATTTCGGTCAGTGTT	114804
rs111804699	snp	A/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76199879	TAAAGTGCTTTTTGT[A/T]AGAACATAAAAACAA	114804
rs111819139	snp	A/C	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76225300	AACCAGCCTGGGCAA[A/C]ATAGCAAGACTCCAT	114804
rs111864209	snp	A/G	0.0142736	0.0832652	intron-variant	RNF157	GRCh38.p7	17:76224675	GAAGAATGGTCTTAC[A/G]CCACACTTGAAATAC	114804
rs111864495	snp	A/G	0.0142736	0.0832652	intron-variant	RNF157	GRCh38.p7	17:76215757	ATTAAACAAGCAGGA[A/G]AACATTCTTTGAGAG	114804
rs111912783	in-del	-/A	0.390277	0.206936	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153123	CCCTCTTTTTTTCTC[-/A]GTGAAACAGAGAGAA	114804
rs111915535	snp	A/C	0.00755907	0.0610114	intron-variant	RNF157	GRCh38.p7	17:76216894	AGACCCTGTGTCAAA[A/C]AAAAACAAAAACAAA	114804
rs111975071	snp	A/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76220388	CGTAATGATATCTAA[A/T]AAAAAAAAAAAAAAA	114804
rs112057189	snp	A/G	0.0279526	0.114869	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147881	TTCCGTTCATGTCTC[A/G]GTTTTTGGGATATCA	114804
rs112094929	snp	A/G/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76207257	AGACCCTGTCTCTAC[A/G/T]AAAAAAATTTTAAAA	114804
rs112106405	snp	A/G/T	0	0	intron-variant	RNF157	GRCh38.p7	17:76227029	ACCCTGAGGGCGGGG[A/G/T]GGAGGGAAGGCGTGC	114804
rs112118456	snp	C/G	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76207280	TTTTAAAAATTAGCC[C/G]AGTGTAGTAGCATGC	114804
rs112142173	snp	A/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76202128	CTCTCTCTCTCTCTC[A/T]CACACACACACACAC	114804
rs112167191	snp	C/T	0.0138799	0.0821421	intron-variant	RNF157	GRCh38.p7	17:76184160	AGTGCCACTGTACTC[C/T]AGCCTGGGCGACAGA	114804
rs112175529	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76201147	TAAAATACTTTTCAT[G/T]TAAAAATGAAAACAC	114804
rs112186122	snp	A/G	0.0607341	0.163335	intron-variant	RNF157	GRCh38.p7	17:76226418	GGGGGCACCTTATTA[A/G]TCTCCTGGACTAGGG	114804
rs112217628	snp	C/T	0.0607341	0.163335	intron-variant	RNF157	GRCh38.p7	17:76227600	TAAGAGGTAGTGGCC[C/T]GGCATGGTGGCTCAC	114804
rs112237060	snp	A/C	0.5	0	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153526	GGAGGGGCCTCAGAG[A/C]AGCAGGGGGAAGAGT	114804
rs112248939	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76187258	GTGCGATCTCGGCTC[A/C]CCACAACCTCCGCCT	114804
rs112277602	snp	A/G	0.0142736	0.0832652	intron-variant	RNF157	GRCh38.p7	17:76232049	TGTTTTTGAAGTTAA[A/G]TCATGTTGTATAGCA	114804
rs112282309	snp	A/G	0.00914312	0.0669923	intron-variant	RNF157	GRCh38.p7	17:76225989	AGTTTCTCACCCTTT[A/G]CTTTTGCTGCTACCA	114804
rs112310617	snp	A/G	0.0193772	0.0965046	intron-variant	RNF157	GRCh38.p7	17:76200174	GTGAACCTGGGAAGC[A/G]GAGCTTGCAGTGAGC	114804
rs112328827	snp	A/C/G	0	0	intron-variant	RNF157	GRCh38.p7	17:76226207	AGGGATCATGGCAAC[A/C/G]TAAGCAGTGGAGTCC	114804
rs112362293	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76203821	CGCCCAGGCTGGAGT[A/G]CAGTGGCACGATCTC	114804
rs112374319	snp	C/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76172063	GTCGGGGGACTGTTC[C/T]GCAGCAGACAGGTAC	114804
rs112411199	snp	A/T	0.0225045	0.103662	intron-variant	RNF157	GRCh38.p7	17:76175982	TCCACCCCTATACTT[A/T]AGGCTCTCCCTGTAC	114804
rs112450628	snp	A/C	0	0	intron-variant	RNF157	GRCh38.p7	17:76177393	CTCTGATCTTAGAGC[A/C]GTGTGGGGCCAAGCC	114804
rs112454918	snp	C/T	0.0146672	0.084371	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76154712	CATCCAGATCCTCCA[C/T]TGACAGGAGTTGGCT	114804
rs112467060	snp	A/G	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76173292	CTCCGTCTCAAAAAA[A/G]AAAAGAAAAGAAAAA	114804
rs112492687	snp	A/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76211876	TATATCAAGAGAAAA[A/T]TTTTCAGTCATTCAT	114804
rs112572615	snp	C/T	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76191877	GACCATCTTAGAGAA[C/T]GAAGTGTGCTGCTTA	114804
rs112594629	in-del	-/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76205145	TTCTTTTTTTCTTTC[-/T]TTTTTTTTTTTTTGA	114804
rs112621669	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76226414	CTGGGGGGGCACCTT[A/G]TTAGTCTCCTGGACT	114804
rs112660155	snp	A/G	0.0573587	0.15934	upstream-variant-2KB	RNF157	GRCh38.p7	17:76240885	CCGCGAGGACTGGCC[A/G]GGAGCTCGCTCGCCA	114804
rs112669579	snp	A/C	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76180374	AAGCAAGGCACAGAT[A/C]CCCCTAATCTATTCA	114804
rs112703229	snp	C/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76233061	GAGTAGCTGTGACTA[C/T]AGGTACCGGCCACCA	114804
rs112747243	snp	A/C	0.0185938	0.0946107	intron-variant	RNF157	GRCh38.p7	17:76197475	TGAGACCACCCTGGG[A/C]AACACAGCAAGACCC	114804
rs112752224	snp	C/T	0.248471	0.249995	intron-variant	RNF157	GRCh38.p7	17:76235444	ACCTCGTGATCTGCC[C/T]GCCTCGGCCTCCCAA	114804
rs112762955	snp	C/G	0.039522	0.134904	intron-variant	RNF157	GRCh38.p7	17:76238071	CCTGGGCGTGACAGA[C/G]AGAGACGATGACTCA	114804
rs112762984	snp	A/C	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76239149	AAGCAGACAGAATGT[A/C]GCAGCCATTCATCCT	114804
rs112795063	snp	G/T	0.5	0	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213622	GATGTCTTTTTTTTT[G/T]GTCTTTACATATGCT	114804
rs112799103	snp	A/G	0.00557542	0.0525036	intron-variant	RNF157	GRCh38.p7	17:76179709	AAACAAAAAATAAGT[A/G]TCTTATTTCAACCTA	114804
rs112806694	snp	A/G	0.00557542	0.0525036	intron-variant	RNF157	GRCh38.p7	17:76189724	AAAGGGAGAGGTTGG[A/G]TTCTCAGATCCTGGA	114804
rs112856086	snp	A/G	0.0142736	0.0832652	intron-variant	RNF157	GRCh38.p7	17:76221987	ATCCACAGAGAGAGT[A/G]GACTGGTGATTGCCA	114804
rs112873016	snp	A/G	0.00795532	0.062565	intron-variant	RNF157	GRCh38.p7	17:76220430	GAAGGATGCTAGTAA[A/G]CCAATTCATTATTTT	114804
rs112912026	snp	C/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76193555	ACCACCCCCCACCCA[C/T]GGACACATACAAGTT	114804
rs112940458	snp	C/T	0.00557542	0.0525036	intron-variant	RNF157	GRCh38.p7	17:76157348	CCAGGCTGCACACTG[C/T]GGTCGGGTGGGCCTT	114804
rs112946225	snp	C/T	0.0236746	0.106192	intron-variant	RNF157	GRCh38.p7	17:76165969	AGGGATGAGCCACTA[C/T]GCCCAGCTAAACCAC	114804
rs112968005	in-del	-/G	0.5	0	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212549	ATCTAGTAAAAAAAA[-/G]AAAGCTGATTTTTAA	114804
rs113048439	snp	G/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76187237	CACCCAGGCTGGAGT[G/T]CAGTGGTGCGATCTC	114804
rs113057529	snp	A/C	0.0150606	0.0854603	intron-variant	RNF157	GRCh38.p7	17:76166357	TGACTCACAGTCACA[A/C]ACACCCACAAAGAAG	114804
rs113060429	snp	G/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76188231	CCAAGGTGACTTACG[G/T]TCTCTTGTACTGCAT	114804
rs113091544	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76179334	AGGAGATTGAGGCTG[C/G]AGTGAGCTATGATAG	114804
rs113157088	snp	A/C			splice-donor-variant	RNF157	GRCh38.p7	17:76212363	CTGATTACAGCCATA[A/C]CACAACTGGTCTGTT	114804
rs113166012	snp	C/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76230273	GATCTTGAGGCAAAG[C/T]AAAGCAACCAGCCGA	114804
rs113207317	snp	C/T	0.0134861	0.0810011	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76152197	GGACTCTCCCAGGCC[C/T]TCTTACTTCCTTCAG	114804
rs113224467	snp	A/T	0.0142736	0.0832652	intron-variant	RNF157	GRCh38.p7	17:76215316	CAAAAAATAAATAAA[A/T]ATACAAAAATTAGTT	114804
rs113304440	snp	C/T	0.352721	0.227922	intron-variant	RNF157	GRCh38.p7	17:76177027	CCTGGGCAGATGGCC[C/T]GGCCCAGGCCCAGGC	114804
rs113340288	snp	A/G	0.0189856	0.0955633	intron-variant	RNF157	GRCh38.p7	17:76203720	GCCTCCCAAAGTGCT[A/G]GGATTACAAGCATGA	114804
rs113362382	snp	A/G	0.5	0	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241173	GCTCCTTGTAGCCCT[A/G]AAGTTAGGAGAACAT	114804
rs113413351	snp	A/G	0.0349115	0.127424	intron-variant	RNF157	GRCh38.p7	17:76194872	TACAAAAAATTAGCC[A/G]GGCGTGGTGGCGGGC	114804
rs113452732	snp	C/T	0.5	0	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241448	GTCTGGTGTTTTTTT[C/T]CCTGAGAGAGTGGAC	114804
rs113452946	in-del	-/CAGTGCT	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76224571	AATTCTATAATGCTA[-/CAGTGCT]CAGTGCTGCTTTTGT	114804
rs113486091	snp	C/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76176965	GCCCGTCTGGGGCTG[C/T]GCCCCCAGGTCTGCC	114804
rs113504427	snp	C/T	0.0142736	0.0832652	intron-variant	RNF157	GRCh38.p7	17:76234755	CTTATATATTCTAGA[C/T]ACAAATTCTTGTCAT	114804
rs113532773	snp	A/G	0.0154538	0.0865337	intron-variant	RNF157	GRCh38.p7	17:76172448	AACACAAAATTAACC[A/G]GGCGTGGTGATGCAT	114804
rs113577534	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76171144	TGATCCGCCCGCCTT[A/G]GCCTCCCAAAGTGCT	114804
rs113593430	in-del	-/TGTTT	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76170237	GATCCACTCACCTGC[-/TGTTT]TGTTTTGAGACAGGG	114804
rs113599611	snp	C/T	0.0622301	0.165053	intron-variant	RNF157	GRCh38.p7	17:76228830	GGAGGCTGAGGCAGG[C/T]GGAGAATCACCTGAA	114804
rs113645343	snp	C/T	0.279461	0.248258	intron-variant	RNF157	GRCh38.p7	17:76233065	AGCTGTGACTACAGG[C/T]ACCGGCCACCACGCC	114804
rs113655087	snp	A/G	0.5	0	missense, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156308	TTCTCACTTTCTGGA[A/G]TCACACCACATTCCT	114804
rs113666752	snp	C/T	0.0314385	0.121371	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212682	GCCTGGCCAACATGG[C/T]AAAACCCTGTCTCTA	114804
rs113692487	snp	C/T	0.0391387	0.134304	intron-variant	RNF157	GRCh38.p7	17:76210406	CCATCCTGGCTAACA[C/T]AGTGAAACCCCGTCT	114804
rs113723423	snp	G/T	0.00795532	0.062565	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145884	GGAGGGAGGACAGTG[G/T]GAGGCTCCAGTCCCC	114804
rs113727561	snp	A/G	0.0146672	0.084371	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76152082	GCAAGGCCGTGATGT[A/G]GGGTGGAGAGTGGTT	114804
rs113766547	snp	C/T	0.00795532	0.062565	intron-variant	RNF157	GRCh38.p7	17:76155396	TTCTTCAGAACAAAA[C/T]TGGTGTCAAATAGGA	114804
rs113777862	snp	A/C	0.0150606	0.0854603	intron-variant	RNF157	GRCh38.p7	17:76158230	ATACAGGCTGCATAC[A/C]CTGTTGAATGCATGA	114804
rs113780419	snp	A/T	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76176116	GCAATCAGAGTCTAC[A/T]TGCAACACTCCATGC	114804
rs113799391	snp	A/G	0.148996	0.228688	intron-variant	RNF157	GRCh38.p7	17:76206167	GCCTAGGAAGTCGAG[A/G]CTGCAGTGAGCTGTA	114804
rs113803116	snp	A/G	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76237141	TCTATTTAAGGATAG[A/G]AAAAAGCTACAAACC	114804
rs113814521	snp	A/G	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76215493	AAAAAAAGAAAGAAA[A/G]AAAAAAGAAAAGAAA	114804
rs113816982	snp	C/T	0.5	0	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146390	TCCTCCAGGCCATCT[C/T]GCCTCTCCCCTGGGA	114804
rs113819140	snp	C/T	0.0225045	0.103662	intron-variant	RNF157	GRCh38.p7	17:76181631	TTTTCAAAAAATGGT[C/T]GGGTGCGGTGGCTCA	114804
rs113836286	snp	C/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76173024	GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	114804
rs113838641	snp	A/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76196331	AAACCAGGACAGAAG[A/T]TAGGATTGCGGTTAC	114804
rs113871910	snp	A/G	5.00279e-05	0.00500115	intron-variant	RNF157	GRCh38.p7	17:76159579	TCTCTGAGGACTAGG[A/G]GAATCAGAGACAGGT	114804
rs113888813	snp	C/T	0.0107246	0.0724382	intron-variant	RNF157	GRCh38.p7	17:76203559	CTGGGTTTAAGCAAT[C/T]CTCCTGCCTCAGCTT	114804
rs113889118	snp	G/T	0	0	intron-variant	RNF157	GRCh38.p7	17:76191520	AGGCAGAGAATTGCT[G/T]GAACCCGGAGGTGGA	114804
rs113942173	snp	C/T	0.0275645	0.114116	intron-variant	RNF157	GRCh38.p7	17:76178279	GCATCTCCAAGCTTC[C/T]GGGTGCCACCACATT	114804
rs113946393	snp	C/T	0.0142736	0.0832652	intron-variant	RNF157	GRCh38.p7	17:76234215	CATATCAAATCTTCA[C/T]TCCTTTTTATTGCCA	114804
rs113955484	snp	C/G			upstream-variant-2KB	RNF157	GRCh38.p7	17:76240609	CAGCAGGAGCCGGCG[C/G]CGCGTGCCTCGCGCG	114804
rs113973281	snp	C/G	0.00795532	0.062565	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153677	CTTCCAACTGAAGAT[C/G]TAACTGAGGCCTGAA	114804
rs113981696	snp	C/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76218537	GTGGTCCTAGATACT[C/T]GGGAAGCTAAGGTGG	114804
rs114006177	snp	C/T	0.0295035	0.117819	intron-variant	RNF157	GRCh38.p7	17:76182951	GTATACTTCTGTTGG[C/T]TACTTTTCGCTCTTG	114804
rs114096989	snp	A/G	0.0193772	0.0965046	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151525	GGATTCAAACAACAC[A/G]ATGTGAAGGACAATT	114804
rs114176315	snp	A/G	0.00318978	0.0398085	intron-variant	RNF157	GRCh38.p7	17:76157409	CTTGCTCCGAGCCCC[A/G]ACTTCCTGCTCTGTG	114804
rs114182677	snp	C/T	0.0111196	0.0737302	intron-variant	RNF157	GRCh38.p7	17:76202632	TGTGAGCTATTAGAG[C/T]GCTACTATTTTTTTT	114804
rs114184695	snp	A/C	0.0134861	0.0810011	intron-variant	RNF157	GRCh38.p7	17:76179787	GAAAACTAATGCCTT[A/C]TTGGGACCAAGAAAG	114804
rs114214455	snp	A/C	0.0310518	0.120672	intron-variant	RNF157	GRCh38.p7	17:76171746	TTACAGATAAAAGAA[A/C]CTGAAGCTCAGACAC	114804
rs114250938	snp	G/T	0.0126979	0.078662	intron-variant	RNF157	GRCh38.p7	17:76184389	TATTTGATGCCTGGT[G/T]ATTTTCCCAGCTTTC	114804
rs114253130	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant, synonymous-codon	RNF157, RNF157-AS1	GRCh38.p7	17:76147299	TATGGGGCAGGACTC[C/T]GGAGCTGCGGCTGTT	114804
rs114349071	snp	A/C	0.0111196	0.0737302	intron-variant	RNF157	GRCh38.p7	17:76212287	CTGCTGAACAAGCAA[A/C]TGCAAACTTATTTTT	114804
rs114386509	snp	C/T	0.0111196	0.0737302	intron-variant	RNF157	GRCh38.p7	17:76203368	TCACTGATTGGCCAT[C/T]GTCTTAACCAACATG	114804
rs114392333	snp	A/C	0.00128664	0.0253311	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76158441	GAGCTGTGTCTCCGA[A/C]TCGCTGCAGGAATGC	114804
rs114395891	snp	C/T	0.0130921	0.0798413	intron-variant	RNF157	GRCh38.p7	17:76199253	CTATTCCTTCCTCTA[C/T]TTTCTCTTCCTCCTT	114804
rs114479624	snp	A/G	0.0126979	0.078662	intron-variant	RNF157	GRCh38.p7	17:76181301	AAAATCTCCAATGGC[A/G]CCCTATGCTTAGATG	114804
rs114661240	snp	A/G	0.021333	0.101051	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241337	CTCCTGTTGATAAAA[A/G]CACACACAACAGTGG	114804
rs114685616	snp	A/G	0.0298908	0.118541	upstream-variant-2KB	RNF157	GRCh38.p7	17:76240893	ACTGGCCGGGAGCTC[A/G]CTCGCCATTGTCCTG	114804
rs114689727	snp	A/G	0.030665	0.119967	intron-variant	RNF157	GRCh38.p7	17:76179791	ACTAATGCCTTCTTG[A/G]GACCAAGAAAGATGA	114804
rs114718327	snp	C/T	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76174450	TGAAGTTCTGAGTTG[C/T]TGATAATGATGAGAT	114804
rs114751629	snp	C/G	0.389715	0.207315	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153124	CCTCTTTTTTTCTCA[C/G]TGAAACAGAGAGAAG	114804
rs114825143	snp	C/T	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76178024	AATAAGGCTCCTCTT[C/T]GTCTTGCTCACCCTA	114804
rs114848399	snp	C/T	0.00755907	0.0610114	intron-variant	RNF157	GRCh38.p7	17:76233895	TTCACCTATTTAGTG[C/T]GTACAATCCAATGGT	114804
rs114851339	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76191016	AACATAGTGGGACTG[C/T]TTCTACAAAAAGAAA	114804
rs114878677	snp	C/T	0.0107246	0.0724382	intron-variant	RNF157	GRCh38.p7	17:76167184	CACAGATGGGTCTGA[C/T]AACTTCCTCTGCTCA	114804
rs114881520	snp	C/T	0.00716266	0.059414	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76143267	GAGGAAGGACAGGGA[C/T]CCTCAGGAAGGGGGT	114804
rs114883921	snp	C/T	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76176788	CGCTTGCTCATGGAG[C/T]GCCAGGGCCAGGCCT	114804
rs114891118	snp	C/T	0.00398564	0.0444627	intron-variant	RNF157	GRCh38.p7	17:76170603	AGAGGATCTGCCTAC[C/T]TTGAAGGCAGACTTT	114804
rs114906164	snp	C/T	0.0103295	0.0711199	intron-variant	RNF157	GRCh38.p7	17:76211736	GACCTTCCTAGCACA[C/T]GGTAGCCACTCAATA	114804
rs114907926	snp	A/G	0.0146672	0.084371	intron-variant	RNF157	GRCh38.p7	17:76188494	CCTGAAGAATAAATA[A/G]GTGTCTTAGCATTAA	114804
rs114912174	snp	C/T	0.0310518	0.120672	intron-variant	RNF157	GRCh38.p7	17:76190045	CCAGTGTTCACAGGG[C/T]GGTGTGGGGCCAGGA	114804
rs114929166	snp	C/T	0.0170251	0.090679	intron-variant	RNF157	GRCh38.p7	17:76178503	TGGAGGCGTGGGATA[C/T]AGGCTGGTAGTGTGA	114804
rs114953091	snp	A/G	0.0217236	0.101931	intron-variant	RNF157	GRCh38.p7	17:76216362	CAGGCAACAGGGTTC[A/G]ATTAGAAATGCCCTT	114804
rs114967517	snp	C/T	0.1264	0.217309	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76148255	AAAGATCCAAATTAT[C/T]TTTGCCTTTTTTTTT	114804
rs115035889	snp	A/C	0.0322114	0.122752	intron-variant	RNF157	GRCh38.p7	17:76224223	AATAATTTGCCTAAT[A/C]ATTTTGAATTTAAGT	114804
rs115049892	snp	A/C	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76182632	AATTATTAGGCAATT[A/C]CCAGTAGTCTACAAA	114804
rs115181297	snp	C/T	0.0295035	0.117819	intron-variant	RNF157	GRCh38.p7	17:76231041	CCTCCTGGGCTGAGG[C/T]GATCCTCTTGTTTGT	114804
rs115220134	snp	A/C/T	0.00362445	0.0424202	synonymous-codon, intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152455	ACCTAGAAATGCGCA[A/C/T]GTCCTCTGGCCTGTA	114804
rs115255423	snp	A/C	0.0174175	0.0916809	intron-variant	RNF157	GRCh38.p7	17:76180383	ACAGATCCCCCTAAT[A/C]TATTCATCTAACCAG	114804
rs115264954	snp	C/T	0.00438332	0.0466095	intron-variant	RNF157	GRCh38.p7	17:76215184	TGTGATGGATCTTGC[C/T]TGTAATCCTAAAACT	114804
rs115289827	snp	C/G	0.029116	0.117091	intron-variant	RNF157	GRCh38.p7	17:76177314	AGCCCTCCCACCCCC[C/G]CGCCCCAGCAGGCTC	114804
rs115346679	snp	C/T	0.02016	0.0983543	intron-variant	RNF157	GRCh38.p7	17:76187889	AAGTGTGAGCCACCA[C/T]GCCCAGCCCTGATAG	114804
rs115429785	snp	C/T	0.0111196	0.0737302	intron-variant	RNF157	GRCh38.p7	17:76207053	CTAGATTCCAACTTT[C/T]TTCCACCATCTTTCT	114804
rs115586995	snp	A/G	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76194502	CCCCGAAAGCAGGAC[A/G]CTTCTTAGTGGGCTG	114804
rs115595711	snp	G/T	0.0170251	0.090679	intron-variant	RNF157	GRCh38.p7	17:76182431	GCATTCACATACACA[G/T]GGGCACACACGCATT	114804
rs115622841	snp	C/T	0.00993419	0.0697739	intron-variant	RNF157	GRCh38.p7	17:76238514	ATCACCCAAGATTCA[C/T]ACTTGTACAAATATG	114804
rs115623821	snp	G/T	0.0142736	0.0832652	intron-variant	RNF157	GRCh38.p7	17:76216745	AAAATTAAAAAATTA[G/T]CTGGGTATGATGGCC	114804
rs115627588	snp	C/T	0.0244538	0.107838	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144794	CCCTTTCCACAGGAG[C/T]GATCCTCCAGCCCTA	114804
rs115632951	snp	A/G	0.0115144	0.0749975	intron-variant	RNF157	GRCh38.p7	17:76222384	AGAATAGAGGTAGTG[A/G]ATTGTGCAACACTGT	114804
rs115634459	snp	A/G	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76189402	CTATGAGCAGAAGGC[A/G]TGGGTCTCAGCTCCT	114804
rs115687182	snp	C/T	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76178048	CACCCTATGTTTGTC[C/T]GTGTATCTCATTCTT	114804
rs115693943	snp	A/G	0.0189856	0.0955633	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151037	AGCCAGGCCAGGAGC[A/G]GGAAGGCAGGGAGTG	114804
rs115809194	snp	C/T	0.0182019	0.0936463	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147586	GATCTGAAGTCTGCT[C/T]TCCTGGCCTCTTGGT	114804
rs115815392	snp	A/G	0.0287284	0.116357	intron-variant	RNF157	GRCh38.p7	17:76231452	TTGAGGCCCACCACC[A/G]TGCCTGGCTAATTTT	114804
rs115879430	snp	C/T	0.0356815	0.128715	intron-variant	RNF157	GRCh38.p7	17:76169290	GCTCCCTGTTTTTAA[C/T]TTCTAAAAGCTATTT	114804
rs115933240	snp	A/G	0.0142736	0.0832652	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76214097	TGGTTGGTTAGTTGG[A/G]AGCACAGGTAAAACA	114804
rs116013549	snp	C/T	0.0170251	0.090679	intron-variant	RNF157	GRCh38.p7	17:76228221	ACACAGACTGAACAA[C/T]GGTAGCTTCACAGCA	114804
rs116066965	snp	A/G	0.0103295	0.0711199	intron-variant	RNF157	GRCh38.p7	17:76238251	TATATGCAAGCTCAC[A/G]TAAGGTTTCAAATAC	114804
rs116116498	snp	G/T	0.0138799	0.0821421	intron-variant	RNF157	GRCh38.p7	17:76207441	GGGAAAAAAAAAAAT[G/T]GGCTTTGATGGATTA	114804
rs116116942	snp	A/C	0.0168055	0.0901129	intron-variant	RNF157	GRCh38.p7	17:76177899	AGGATGACCTTCCTG[A/C]GGAAAAGAGCTTCCC	114804
rs116280632	snp	A/G	0.0622301	0.165053	intron-variant	RNF157	GRCh38.p7	17:76210322	GAACCCGCCGGGCGC[A/G]GTGGCTCATGCCTGT	114804
rs116286837	snp	C/G	0.030665	0.119967	intron-variant	RNF157	GRCh38.p7	17:76193397	AATACAAGCAATTAG[C/G]TAAGTATCTCTTATC	114804
rs116286995	snp	C/T	0.0189856	0.0955633	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153781	CTGTCTCCTTGACCA[C/T]GCCTTTAGTACGTCT	114804
rs116496940	snp	C/G	0.0115144	0.0749975	intron-variant	RNF157	GRCh38.p7	17:76210183	AGTAACAAAATCAAA[C/G]AGTAGACATCTGATA	114804
rs116528313	snp	A/G	0.0146672	0.084371	intron-variant	RNF157	GRCh38.p7	17:76188252	TGTACTGCATCCCAC[A/G]GCCTCCTACCTGGGA	114804
rs116531785	snp	A/C	0.0170251	0.090679	intron-variant	RNF157	GRCh38.p7	17:76181646	CGGGTGCGGTGGCTC[A/C]CATCTAATCCCAGCA	114804
rs116533079	snp	C/T	0.00398564	0.0444627	intron-variant	RNF157	GRCh38.p7	17:76177145	CCCCGGCCCTGGCCC[C/T]GGCCCAGTGAGGACC	114804
rs116588094	snp	A/G	0.029116	0.117091	intron-variant	RNF157	GRCh38.p7	17:76212102	GGAAAAGGGTTGCCT[A/G]AAGAGGTGACAGGGA	114804
rs116599401	snp	G/T	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76239216	AAAATAAAACTACTT[G/T]CAATTAAAAGTAAAC	114804
rs116600617	snp	A/G	0.029116	0.117091	intron-variant	RNF157	GRCh38.p7	17:76233908	TGTGTACAATCCAAT[A/G]GTTTTTAGTATATTG	114804
rs116679878	snp	A/G	0.0170251	0.090679	intron-variant	RNF157	GRCh38.p7	17:76170038	GACTTGGGGATCCTG[A/G]GCTTCACTGTGGGCT	114804
rs116684370	snp	C/T	0.0111196	0.0737302	intron-variant	RNF157	GRCh38.p7	17:76209235	TGTGCCCAGCTTGAT[C/T]TTCTTTGGGAAAAAG	114804
rs116695300	snp	C/T	0.00478085	0.0486577	intron-variant	RNF157	GRCh38.p7	17:76234924	AAACCACTATCCTTT[C/T]CCCATTCAATTGTCT	114804
rs116728768	snp	A/C	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76230039	AATCATTAGTAAAAT[A/C]CATATTCTGAATATA	114804
rs116744373	snp	A/T	0.0170251	0.090679	intron-variant	RNF157	GRCh38.p7	17:76225215	TACATGTTAGGTGCA[A/T]TGGCTCACAACTGTA	114804
rs116745555	snp	C/T	0.0158469	0.0875917	intron-variant	RNF157	GRCh38.p7	17:76188026	AGCTTCTAAGAGTCT[C/T]GAGAGCTCTGATTAT	114804
rs116831271	snp	C/T	0.0248432	0.108648	utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76143179	TCTAACCTAGGTATG[C/T]CTTGGACATGGGACT	114804
rs116843146	snp	C/T	0.00874735	0.0655527	intron-variant, nc-transcript-variant	RNF157	GRCh38.p7	17:76156481	TTCTCTCTTCCGTCC[C/T]CACTTCAGCCCAAGC	114804
rs117025238	snp	A/C	0.0107246	0.0724382	intron-variant	RNF157	GRCh38.p7	17:76186659	ATCTCAGGTCTGGGC[A/C]GGGGGGGCAGTGGCT	114804
rs117064698	snp	C/T	0.00557542	0.0525036	intron-variant	RNF157	GRCh38.p7	17:76176748	AGAGGAGCCCCGAGG[C/T]GGAGCTGGGCCTTGG	114804
rs117084109	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76185049	CATCATAAAATGGCA[C/T]AGATCTTGGTAATGA	114804
rs117104101	snp	A/G	0.0138799	0.0821421	intron-variant	RNF157	GRCh38.p7	17:76216306	ATGATTGAACCTAGC[A/G]AGAGAGGACCCCTAA	114804
rs117130497	snp	C/T	0.00105397	0.0229319	synonymous-codon, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154290	TTTACCACCTTCCTG[C/T]GTGGGTGATCCATCC	114804
rs117169554	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76144985	GAACATCAATATACC[A/G]TGAGGACATTCCAGA	114804
rs117200915	snp	C/T	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76201306	GCCTTGGCAACATAG[C/T]GAGACCCTAGTCTCT	114804
rs117235875	snp	A/G	0.0126979	0.078662	intron-variant	RNF157	GRCh38.p7	17:76157315	CCCTCTCCTGGCTGG[A/G]TCTGTCTCCCGTCTA	114804
rs117348350	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142754	TGTGGTGGTCTGTGC[C/T]CAGGAGATGCCTCAG	114804
rs117578348	snp	C/T	0.00795532	0.062565	intron-variant	RNF157	GRCh38.p7	17:76160542	TGATTTTTAATGTGG[C/T]TGAACTTTTTAAAAA	114804
rs117647154	snp	C/T	0.0165278	0.0893908	intron-variant	RNF157	GRCh38.p7	17:76187038	ATATATCAATGGAAA[C/T]AGTTAAGTTTATAAG	114804
rs117673569	snp	A/C	0.00478085	0.0486577	intron-variant	RNF157	GRCh38.p7	17:76219850	TGGTGACAGTATTTT[A/C]TTCCGAGAATGTGGC	114804
rs117750592	snp	A/G	0.0119091	0.0762411	intron-variant	RNF157	GRCh38.p7	17:76208698	AAAACATTTGCCAGC[A/G]CGGTGGCTCACACCT	114804
rs117813251	snp	A/T	0.00597247	0.0543191	intron-variant	RNF157	GRCh38.p7	17:76201850	ACCATTCCACTATAA[A/T]GGCCATTAGATATTT	114804
rs117894597	snp	C/G	0.00914312	0.0669923	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151923	CCTCTCTGATCCTAG[C/G]TGAAACACATTTCTT	114804
rs117910608	snp	A/G	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76173851	CCACAGCTGTCCCTC[A/G]CTTTACAGTTTGCCA	114804
rs117926104	snp	C/T	0.0573587	0.15934	intron-variant	RNF157	GRCh38.p7	17:76208896	GGAGAATCACTTGAG[C/T]CTAGGAGACTGTGGC	114804
rs117945910	snp	C/T	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76233382	GGTAATGTTTTTAAT[C/T]TCGAAGAAATCCAAT	114804
rs117997344	snp	C/T	0.0387552	0.1337	intron-variant	RNF157	GRCh38.p7	17:76179173	CTGAGGCAGAAAGAT[C/T]GCTTGAGCTTAGGAG	114804
rs118026392	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76222092	GGCCGGGCGCAGTGG[C/T]GCACACCTTTTGGGA	114804
rs118159721	snp	C/T	0.0197687	0.0974348	intron-variant	RNF157	GRCh38.p7	17:76166436	AGCAGTGTGCACAGC[C/T]AAAGAGGACAGAAAT	114804
rs137922762	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76181598	GTTCTAAAATATGGC[A/G]ACTTCTTCACTAAAT	114804
rs137950728	snp	C/G	0.00597247	0.0543191	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144095	AAGGGGGTAGAGATG[C/G]GGGCAACAGGGACAA	114804
rs137960795	snp	C/T			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213743	TTTCAGCCCATCCCC[C/T]AACCACTGAGGAAGG	114804
rs137981342	in-del	-/GC			intron-variant	RNF157	GRCh38.p7	17:76205913	TATAAAATGAGAGGA[-/GC]GGTTTGAACTCCTGC	114804
rs138002955	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76171683	TTTTCCCTTCTGTTA[A/C]CTTAATTTTGACAAC	114804
rs138062162	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76225829	GATCTCCTTGGCCAG[A/G]GAATCTGCCCTCTCT	114804
rs138096340	snp	C/T	0.00914312	0.0669923	intron-variant	RNF157	GRCh38.p7	17:76188190	GTTCTAGATGGTGAA[C/T]ACCCATACTCTATCA	114804
rs138161667	snp	C/T	3.29826e-05	0.00406082	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159389	CTGTCAGACAGGCGG[C/T]CAAGAGGCGAGATCG	114804
rs138171913	snp	A/G	0.00119737	0.0244387	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153158	ACAAATCCATTCCAC[A/G]GGCTAGGGAATGTCG	114804
rs138185227	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76193729	ACTTCTGAAGCCTGA[C/T]CCGAAACAATCAGGA	114804
rs138224301	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76182512	TAGATTTTTTTTTTT[-/T]ACCATTCTGATTTCA	114804
rs138236457	snp	C/T	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76193466	TATATCTCACTTGGT[C/T]GTGACCCAGAAGAAT	114804
rs138242013	snp	C/T	0.0134861	0.0810011	intron-variant	RNF157	GRCh38.p7	17:76232520	CACTTGGATTATTTC[C/T]AGTTTCTTGGCTATT	114804
rs138279435	snp	A/G	0.00398564	0.0444627	intron-variant	RNF157	GRCh38.p7	17:76177981	AGAGCTACCCACTGC[A/G]GGTATCCTCTGAGCT	114804
rs138332011	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76237910	CAATATGGTGAAACC[C/T]CATCTCCACTAAAAA	114804
rs138367333	snp	A/G	0.000116197	0.00762135	intron-variant	RNF157	GRCh38.p7	17:76159303	TTCATCAAGGATTCC[A/G]GGGGCAACAGTGTGG	114804
rs138391323	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149277	TCTCCTGGCAGAGCC[C/T]GTGAGCAAGGTGCAG	114804
rs138462744	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76198668	TGGTTACCCTGTATC[C/T]GTTCTCATGACTCTC	114804
rs138468066	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76206135	ACTGGAGAATCTGAG[A/G]TGGGAGGATCACTTA	114804
rs138496601	in-del	-/AT			intron-variant	RNF157	GRCh38.p7	17:76185977	TTAAAAATATAAAAC[-/AT]ATATATATATATTTC	114804
rs138516306	snp	C/T	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76170969	ACAATCTCGCCTCAC[C/T]GCAACCTCTGTCTCC	114804
rs138521829	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76219580	AGATTTCTTTGAATA[C/T]GCATTGCTTTATGTA	114804
rs138554476	snp	C/T	0.00636936	0.0560724	intron-variant	RNF157	GRCh38.p7	17:76206900	TTTGTCCAGCAATTA[C/T]AAGGAATCTTCCAAG	114804
rs138595809	snp	C/G	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76167229	TATCAACAGGGTCTA[C/G]CGAAGAGAAGAAAGG	114804
rs138618985	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76187890	AGTGTGAGCCACCAC[A/G]CCCAGCCCTGATAGT	114804
rs138629684	snp	C/T	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76178319	CAACCGGGAGAGCTG[C/T]TTGCAGTGCACCTGG	114804
rs138702366	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76237997	ACTGAGGCGGGAGAA[C/T]TGCTTGAACCCTAGA	114804
rs138742475	snp	C/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76214383	ATCCGCAGACGCACA[C/G]ATTTCTTTGCCTAGA	114804
rs138774231	snp	C/T	0.0103295	0.0711199	intron-variant	RNF157	GRCh38.p7	17:76229998	TGCATTTCTATAAGG[C/T]ACACCCCAACTCATC	114804
rs138805084	snp	A/G	0.258565	0.249853	intron-variant	RNF157	GRCh38.p7	17:76237847	GCACTTTGGGAGGCC[A/G]AGGCAGGCGGATCAC	114804
rs138902853	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142777	TGCCTCAGCGGGGGT[A/G]GAAACTCTGGTGGGA	114804
rs138912015	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76198079	ACCTTCCTTTCTGGC[C/T]ACCCAACCATAATTA	114804
rs138918491	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76159931	TGTGTACTATTTACA[C/T]AGTTTTGATCAATCT	114804
rs138955578	snp	A/G	0.00914312	0.0669923	intron-variant	RNF157	GRCh38.p7	17:76157031	GAGTGCAGTGGTGCG[A/G]TCTTGGCTCACTGCA	114804
rs138970178	snp	A/T	0.0158469	0.0875917	intron-variant	RNF157	GRCh38.p7	17:76202038	AAAGGACAAAAAAAA[A/T]TTGTAGTAAAATTAT	114804
rs138970952	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76229485	AGCCCAGTGGGCAAC[G/T]GATAAATTTTGGCTT	114804
rs139074635	snp	A/G	0.0298908	0.118541	intron-variant	RNF157	GRCh38.p7	17:76231146	GTGACTACAGGCACC[A/G]GCCACAACGCCCAGC	114804
rs139079442	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76157410	TTGCTCCGAGCCCCG[A/G]CTTCCTGCTCTGTGC	114804
rs139137052	snp	G/T	0.00557542	0.0525036	intron-variant	RNF157	GRCh38.p7	17:76215147	AGTTGCAATTTTTGT[G/T]GAAGATTTGTAGCAG	114804
rs139185241	snp	A/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76162719	TTTTGGTAACCAAGG[A/T]CTACCGATTCATAAT	114804
rs139205553	snp	C/T	0.0836354	0.186609	intron-variant	RNF157	GRCh38.p7	17:76203988	TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG	114804
rs139240526	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76185185	ACACCTACATGGCTA[C/T]GTGAACTGCTTAGAT	114804
rs139254679	in-del	-/AAC	0.0142736	0.0832652	intron-variant	RNF157	GRCh38.p7	17:76235680	TGTGTACTCTAAAAT[-/AAC]AAAAATTTGGAGAAT	114804
rs139285422	snp	A/G	0.00835141	0.0640778	intron-variant	RNF157	GRCh38.p7	17:76172540	AGGTTGCAGTGAGCC[A/G]AGATCGCAGTGAGCC	114804
rs139391612	snp	A/G	0.0260105	0.111035	intron-variant	RNF157	GRCh38.p7	17:76226922	TTAAGCCGCTGGGGG[A/G]TGCCGCTGCAGAGCC	114804
rs139399256	snp	A/G/T	0.0198051	0.0977972	intron-variant	RNF157	GRCh38.p7	17:76173015	AAGAAGGCTGGGCGC[A/G/T]GTGGCTCACGCCTGT	114804
rs139400380	snp	A/G			intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76148755	TTTGTATTTTCTGTA[A/G]AGATGGGGTTTCACT	114804
rs139415450	snp	C/T	4.58306e-05	0.00478677	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76173765	GTCTTCACGGGTTCT[C/T]GGGGAGGTGGGGCGG	114804
rs139449789	snp	C/T	0.00755907	0.0610114	intron-variant	RNF157	GRCh38.p7	17:76239379	AGTGAAGGGATGATT[C/T]TAATAACAAACATAC	114804
rs139469687	snp	C/G/T	0.000135146	0.00821932	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76162560	AACTTACCTTAGAAT[C/G/T]TTGTGTGTTGTACTT	114804
rs139489743	snp	G/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76235510	GCCGTAAATTGCATA[G/T]TTTTAAGTGTATGGT	114804
rs139561737	snp	A/G	0.0142736	0.0832652	intron-variant	RNF157	GRCh38.p7	17:76179306	GGCTGACGCAAGAGG[A/G]TCACTTGAGCCCAGG	114804
rs139565621	snp	C/T	0.00914312	0.0669923	intron-variant	RNF157	GRCh38.p7	17:76199959	CTAGGCATTTCAGGT[C/T]GGGCGCGGTGGCTCA	114804
rs139604964	snp	C/G	0.00914312	0.0669923	intron-variant	RNF157	GRCh38.p7	17:76200164	GGAGAATGCTGTGAA[C/G]CTGGGAAGCGGAGCT	114804
rs139649300	snp	C/T	0.00636936	0.0560724	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145117	TACAGGTTGTAACAG[C/T]TGTCACAGGAGGGTA	114804
rs139683475	snp	C/T	0.0107246	0.0724382	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151088	CAGCTCCAGTCCAGG[C/T]CTAACTGGCAGGAGG	114804
rs139699038	snp	C/T	1.64765e-05	0.00287019	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167765	TTAGCTTTACTGGCC[C/T]CTTCTCCAGGGCTCT	114804
rs139733689	snp	C/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76155076	GACAGTCCACAGGCC[C/T]GGGAGCAGCTGCTCT	114804
rs139780955	snp	C/T	0.0023933	0.0345097	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151628	TTTGGAGCCCTTGAA[C/T]GGGCACACTAACTAA	114804
rs139781259	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194491	TGCTGAAAGACCCCC[A/G]AAAGCAGGACGCTTC	114804
rs139871175	snp	C/G	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76211149	CTTATTTGTTCCAGG[C/G]AAGAACAAACCATGC	114804
rs139884477	snp	C/T	0.000135325	0.00822459	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155666	CAGACATGGAGGAGA[C/T]GGTGTCAGTGCTGAT	114804
rs139895879	in-del	-/AAAT			intron-variant	RNF157	GRCh38.p7	17:76205753	ATAAATAAATAAATA[-/AAAT]AATAAATAAAATAAT	114804
rs139917326	snp	A/G	0.00557542	0.0525036	intron-variant	RNF157	GRCh38.p7	17:76207977	GTTGCCCAGGCTGCA[A/G]TGATCATAGCTCACT	114804
rs139925038	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150408	TGGAGTAACTATCAA[C/T]AAGCAGGTTAGCTGG	114804
rs139947921	snp	C/T	0.00755907	0.0610114	intron-variant	RNF157	GRCh38.p7	17:76222174	AACATGAAGCAACCC[C/T]GTCTCTACTAAAAAT	114804
rs139955597	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76172053	CCTGGGTCAGGTCGG[A/G]GGACTGTTCTGCAGC	114804
rs139975433	snp	G/T	0.213635	0.247341	intron-variant	RNF157	GRCh38.p7	17:76210529	CGGGAGGCAGAGCTT[G/T]CAGTGAGCCAAGATC	114804
rs139975835	snp	C/G	0.00676609	0.0577691	intron-variant	RNF157	GRCh38.p7	17:76169425	TTTTGTTTCCAATTA[C/G]ATTTTTTTTACTTTA	114804
rs139989539	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76215456	CCAGCCTGGGTGACA[C/G]AGTGAGACCCTCTCT	114804
rs140024857	snp	A/G	0.0189856	0.0955633	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145881	CCTGGAGGGAGGACA[A/G]TGTGAGGCTCCAGTC	114804
rs140080290	in-del	-/TG/TGTG/TGTGTG	0.417683	0.185425	intron-variant	RNF157	GRCh38.p7	17:76182451	CACACGCATTTAGTC[-/TG/TGTG/TGTGTG]TGTGTGTGTGTGTGT	114804
rs140086274	snp	C/T	0.030665	0.119967	intron-variant	RNF157	GRCh38.p7	17:76225125	TGCAGTGAGCCAAGA[C/T]TGCACTACTGCACTC	114804
rs140091781	snp	C/T	0.000692007	0.0185883	missense, intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152406	GTGCTTTCACGCTTG[C/T]GATGTCAAAGTCATT	114804
rs140127777	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76156808	TCCTCCCACACCCCC[A/C]CCTCCGATCCCAGCC	114804
rs140168371	snp	A/G	0.0126979	0.078662	intron-variant	RNF157	GRCh38.p7	17:76190376	TTCGCCATGTTGGCC[A/G]GGCTGGCCTCAAACC	114804
rs140189005	snp	C/T	1.65042e-05	0.0028726	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76158429	CGGTCTCTGAGAGAG[C/T]TGTGTCTCCGACTCG	114804
rs140269268	snp	A/G	0.00597247	0.0543191	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76143230	CGTGCTTCTCCCTAG[A/G]AGAGGACTAAGCACC	114804
rs140270949	snp	C/T	0.0126979	0.078662	intron-variant	RNF157	GRCh38.p7	17:76186524	AAACAAAAAACAAAA[C/T]GAAACAAAAAAACCC	114804
rs140291649	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76181242	AAAGTTATACCATCA[A/T]GGCAAACAGTACTGA	114804
rs140335714	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76197899	TGGGAACGTCTGTGT[A/G]TATTTATTTGAGGAA	114804
rs140352908	snp	C/T	0.0138799	0.0821421	intron-variant	RNF157	GRCh38.p7	17:76167851	TCAATATTTTAAAAT[C/T]TACCTTTAAAAAAAT	114804
rs140360605	snp	C/T	0.00676609	0.0577691	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241649	AGTCTCCCTCTGTCG[C/T]CCAGGCTGGAGTGCA	114804
rs140404141	snp	A/G	0.248755	0.249997	intron-variant	RNF157	GRCh38.p7	17:76235267	CAGTGGCACGATCTC[A/G]GCTCACTGCAAGCTC	114804
rs140445220	snp	A/G	0.00438332	0.0466095	intron-variant	RNF157	GRCh38.p7	17:76161739	GATCCCTCCCAGCGC[A/G]CATCCGTTTGTCAGA	114804
rs140504201	snp	A/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76172820	ACAGCCTTGGTAGAC[A/T]TATCATCTAGGGGTG	114804
rs140541212	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76237867	AGGCGGATCACCTGA[A/G]AGGTCAGGAGTTCAA	114804
rs140545635	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76217057	CACCTGTTCAATCAC[A/T]CAATAATTCTTTAGC	114804
rs140604754	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76176837	ATGCTTCAGGGGCCC[C/T]GGGCAGGAAGTGGGA	114804
rs140622221	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76201189	AAAATTCAAACAACA[C/T]AGAAGAATATGAAGA	114804
rs140702707	snp	A/G	0.0197687	0.0974348	intron-variant	RNF157	GRCh38.p7	17:76187220	ATGGAGTCTCGCTCT[A/G]TCACCCAGGCTGGAG	114804
rs140843746	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76232242	AAATTTAAAAAATTA[A/G]ATGGGAGTGGTGGCA	114804
rs140912676	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76148849	TGCTGGGATTACAGG[C/T]GTGAGCCACTGTGCC	114804
rs140925770	snp	C/T	0.031825	0.122064	intron-variant	RNF157	GRCh38.p7	17:76218895	GCCAAGATCACACCA[C/T]GGCACTCCAGCCTGG	114804
rs140990696	snp	C/T	0.00676609	0.0577691	intron-variant	RNF157	GRCh38.p7	17:76208398	CTGATCCCTTACAGG[C/T]TGTGCAGTCTTTAAA	114804
rs141003981	snp	A/G	0.00176316	0.029639	intron-variant	RNF157	GRCh38.p7	17:76165565	AAGAAACAAAGGCAC[A/G]TGAGTGAAGAAGCCC	114804
rs141041065	snp	C/G	0.0138799	0.0821421	intron-variant	RNF157	GRCh38.p7	17:76180888	CTTATTTCACATTCT[C/G]GAAAGGAACAACATG	114804
rs141045829	snp	C/T	0.0111196	0.0737302	intron-variant	RNF157	GRCh38.p7	17:76204573	AGAATCATGTTCTCT[C/T]TTTTTGCCACAAAGC	114804
rs141045932	snp	A/G	0.0138799	0.0821421	intron-variant	RNF157	GRCh38.p7	17:76158970	GATTTGTGCCTAGCT[A/G]GATTTAGATGTTTAA	114804
rs141101268	snp	A/G/T	0.00119737	0.0244387	utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142658	AAGTGAGCGACCAGC[A/G/T]TGCTAAACTCCAGGT	114804
rs141119957	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76195231	GGGTAGAGCAAGGCT[A/G]GAAACAGGAGACTGG	114804
rs141160254	snp	C/T	0.00517822	0.0506191	intron-variant	RNF157	GRCh38.p7	17:76193070	GTGATCCTCCCGCCT[C/T]GGCCTCCCAACATGC	114804
rs141209983	in-del	-/A	0.0236746	0.106192	intron-variant	RNF157	GRCh38.p7	17:76199149	GAGAGGGGAAAGAAG[-/A]TCAAAGTTGGCAACA	114804
rs141212004	snp	C/T	0.0283406	0.115616	intron-variant	RNF157	GRCh38.p7	17:76210321	AGAACCCGCCGGGCG[C/T]AGTGGCTCATGCCTG	114804
rs141278852	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76170412	TTTTGTATTTCTTGT[A/G]GAGACAGGGCTTTAC	114804
rs141289837	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76229554	ATCTTCAGCATTTCA[A/G]TCCAAATCTTCAATC	114804
rs141299067	snp	A/G	0.00597247	0.0543191	intron-variant	RNF157	GRCh38.p7	17:76166156	ATTTTTGTATTTTTA[A/G]TAGAGACAGGGTTTC	114804
rs141311405	snp	C/T	0.00993419	0.0697739	intron-variant	RNF157	GRCh38.p7	17:76237242	AGAAGTTCCATTAAA[C/T]ATACTAAGAAAAAAG	114804
rs141337312	snp	C/T	1.64787e-05	0.00287038	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167663	TACCTGGCAATACCA[C/T]TCTGGAACTCTTCCG	114804
rs141366814	snp	A/T	0.0103295	0.0711199	intron-variant	RNF157	GRCh38.p7	17:76224461	CATATATTTGAAAAA[A/T]TCTTCATCTACATGA	114804
rs141371505	snp	A/G	0.0134861	0.0810011	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144668	GCTCTGCCACCAGAA[A/G]GAAGGATTGTTTCCT	114804
rs141388552	snp	G/T	0.00874735	0.0655527	intron-variant	RNF157	GRCh38.p7	17:76226716	CATCTAAGAGACCTA[G/T]GCTTTCTTCAGCCCC	114804
rs141409247	snp	A/G	0.0023933	0.0345097	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154390	GTAAACTGATTGGCT[A/G]AAGACAGAACTAATC	114804
rs141414293	in-del	-/TATA			intron-variant	RNF157	GRCh38.p7	17:76182778	TATATATATATATAT[-/TATA]ATATATATATGAGAG	114804
rs141435254	snp	C/G	0.00597247	0.0543191	intron-variant	RNF157	GRCh38.p7	17:76166933	CCGAGCAGCCCCTTT[C/G]CTGTCAGACCGAGTC	114804
rs141458290	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76231799	ATGGCATAAAATTCA[C/T]CCATTGAACAATTCA	114804
rs141460217	snp	A/T	0.0130921	0.0798413	intron-variant	RNF157	GRCh38.p7	17:76187999	TGGCACTTGTTCCGT[A/T]TTGCATTGCTAAGCT	114804
rs141478677	in-del	-/T	0.205417	0.245993	intron-variant	RNF157	GRCh38.p7	17:76196683	TCTCTGTACCCCTGC[-/T]TGTGGAGAGTTTTGG	114804
rs141523567	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76178495	GTCTCCCTTGGAGGC[A/G]TGGGATATAGGCTGG	114804
rs141536531	snp	A/G	0.00318978	0.0398085	intron-variant	RNF157	GRCh38.p7	17:76171253	GAGTGCAGTGGTACA[A/G]TCTCGGCTCACTGCA	114804
rs141546187	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76198883	ACCCTCTGGATGCCA[C/T]ACCTGCTTATGCTGA	114804
rs141557056	snp	C/G	0.00874735	0.0655527	intron-variant	RNF157	GRCh38.p7	17:76174148	TCACAAAAGGCTTTT[C/G]CATCTGACCTCAGAC	114804
rs141692913	snp	A/G	7.09883e-05	0.00595727	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76173779	TTGGGGAGGTGGGGC[A/G]GCGTAAGGAAACTGT	114804
rs141714594	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76221695	CAAGGAAATAATAGA[C/T]GTTTAAATCATATGG	114804
rs141799978	snp	A/C	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76178881	AGTTGAGGTTTGAAC[A/C]CGTTCTACCTTTATC	114804
rs141820443	snp	C/T	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76190093	GGAGACAAATAACTT[C/T]GTAAAGGGTAGATGT	114804
rs141829528	in-del	-/T	0.0178098	0.0926698	intron-variant	RNF157	GRCh38.p7	17:76192674	TTTTTAAATTAAGGG[-/T]TTGTGGAGTAATACT	114804
rs141854590	snp	A/T	0.00953873	0.0683987	intron-variant	RNF157	GRCh38.p7	17:76201643	TGTGTAGCTATAAAT[A/T]TATGTACATAATGCA	114804
rs141883913	snp	C/T	0.0130921	0.0798413	intron-variant	RNF157	GRCh38.p7	17:76205638	GCTGAAGCAGAAGAA[C/T]TGCTTGAACCTGGGA	114804
rs141902180	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150875	TTGGACGGGGTGAAG[A/C]ATTGGCAGGGAGGAC	114804
rs141936932	snp	C/T	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76158143	TAGCAAGAATATAAA[C/T]GCTACAAGGGCAGGG	114804
rs141947972	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76198532	GAACATACTCTAATT[A/G]CCACACCCTAGATTC	114804
rs141967128	snp	A/G	0.0154538	0.0865337	intron-variant	RNF157	GRCh38.p7	17:76234448	AGAAACTGTCAAACC[A/G]TTTTCCAAAGTGGCT	114804
rs142019894	in-del	-/AT			intron-variant	RNF157	GRCh38.p7	17:76172652	GAGACTCTGTCTCAA[-/AT]ATATATATATATATA	114804
rs142045726	snp	C/T	0.00318978	0.0398085	intron-variant	RNF157	GRCh38.p7	17:76193009	GACTTTTTGTAGAGA[C/T]GGGACCTCGCTGTTT	114804
rs142086697	snp	C/T	0.0821764	0.185298	intron-variant	RNF157	GRCh38.p7	17:76203860	GCAAACTCCGCCACC[C/T]GGGTTCACGCCATTC	114804
rs142099286	snp	A/G	0.00478085	0.0486577	intron-variant	RNF157	GRCh38.p7	17:76230965	TTTTTTAAAGTTAGG[A/G]TCTCACTCTATCACT	114804
rs142136819	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76181510	ACACTGCCAGCAGCC[A/C]CAGCCACAATGGATA	114804
rs142137513	snp	C/G/T	0.0001166	0.00763465	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167026	CCTCTTCGGCCCACT[C/G/T]GGAGGGATCCACGGT	114804
rs142157709	snp	A/G	0.0126979	0.078662	intron-variant	RNF157	GRCh38.p7	17:76193613	GAGATTCTCGGTTTA[A/G]GATCACTAGGGAAAT	114804
rs142178120	snp	A/G	0.000296492	0.012172	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF157	GRCh38.p7	17:76212388	TCTGTTCCCCAGAAA[A/G]TTCAGATCGCTGTTC	114804
rs142235246	snp	A/G	0.0158469	0.0875917	intron-variant	RNF157	GRCh38.p7	17:76156724	GCAGGGTATCTCCAC[A/G]TGGACCCCAGTTAAT	114804
rs142262007	snp	C/T	0.0189856	0.0955633	intron-variant	RNF157	GRCh38.p7	17:76233157	GATCTCCTGACCTCA[C/T]GACCCACCTGCCTCA	114804
rs142307356	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76214141	GATGGGCATCAGAAG[C/T]GGGGGGCAGTCTTGT	114804
rs142330498	snp	C/T	0.00438332	0.0466095	intron-variant	RNF157	GRCh38.p7	17:76211046	CCAACCTCAGGTGAT[C/T]TGTCCACCTCGGCCT	114804
rs142340363	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76176165	GAAAACCAAGAAGAT[A/G]AGGCCCTGCTCTTTC	114804
rs142383206	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76157325	GCTGGGTCTGTCTCC[C/T]GTCTAGTCCAGGCTG	114804
rs142444706	snp	A/C	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76216740	GACAAAAAATTAAAA[A/C]ATTAGCTGGGTATGA	114804
rs142446632	snp	C/T	2.43093e-05	0.00348627	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76173722	GAGCCTCAGTGTGTC[C/T]TTTCGGATATTGACC	114804
rs142464731	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146613	ACGAGGCATCTCTGG[C/T]CGGGGGAGGCCCAGT	114804
rs142480620	in-del	-/ATTCAATT	0.16618	0.23553	intron-variant	RNF157	GRCh38.p7	17:76183734	GAGCTGTCCTTTATC[-/ATTCAATT]ATTCAATTATTTCTT	114804
rs142495727	snp	A/C	0.00517822	0.0506191	intron-variant	RNF157	GRCh38.p7	17:76228146	TCCCCCCACTAATTT[A/C]AATTCTATTCTTATG	114804
rs142506135	in-del	-/CT	0.330249	0.23677	intron-variant	RNF157	GRCh38.p7	17:76169280	TTTCATTTCTGCTCC[-/CT]GTTTTTAATTTCTAA	114804
rs142533215	snp	C/G	0.0185938	0.0946107	intron-variant	RNF157	GRCh38.p7	17:76239550	CACCACCCCCCCCAC[C/G]CCCCGGCTTCTGACA	114804
rs142535283	snp	C/T	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76168865	AAGTATTCTAGATTA[C/T]AAATAATTTCTAAAA	114804
rs142604546	snp	A/G	0.0138799	0.0821421	intron-variant	RNF157	GRCh38.p7	17:76172906	AGAAGGCAAATGACG[A/G]TAATTAACATTGATG	114804
rs142620085	in-del	-/A	0.030665	0.119967	intron-variant	RNF157	GRCh38.p7	17:76195434	AACACTGCTAGTGGG[-/A]AAAAAAAAATTGGTA	114804
rs142642824	snp	G/T	0.0150606	0.0854603	intron-variant	RNF157	GRCh38.p7	17:76172550	GAGCCGAGATCGCAG[G/T]GAGCCGAGATCGTGC	114804
rs142695044	in-del	-/AAG	0.0287284	0.116357	intron-variant	RNF157	GRCh38.p7	17:76163041	AAGAAAAAGAAGAAG[-/AAG]TTGGCAAGGAAAAAG	114804
rs142725536	snp	C/G	0.00318978	0.0398085	intron-variant	RNF157	GRCh38.p7	17:76232765	TTTGACACTGTCTGC[C/G]TTTTCTATTTTAGTT	114804
rs142742113	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76238202	CCAGGTCAATTCAAA[G/T]ATCAGAAGAAAGGCG	114804
rs142752677	snp	C/T	0.000132113	0.00812646	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76159502	AGGAACTGCTGGGGA[C/T]GGGGTGAGGGGCCCG	114804
rs142763564	snp	A/T	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76168193	ACTTGGGTTACTACT[A/T]CTTGATTTTTCAGTT	114804
rs142814544	snp	A/G	0.0111196	0.0737302	intron-variant	RNF157	GRCh38.p7	17:76230515	ATCTCTCTGCTTCCA[A/G]TCTCTCCTCCCAATC	114804
rs142820140	snp	C/T	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76179350	AGTGAGCTATGATAG[C/T]ATCACTGCACTCCAG	114804
rs142899028	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194558	ACAAATAACTCATTT[A/C]AAATAGTCTCTATAG	114804
rs142907410	snp	C/T	0.0103295	0.0711199	intron-variant	RNF157	GRCh38.p7	17:76223761	ATAAAATATGGAATA[C/T]AATGAAACAAAAAAC	114804
rs143071812	snp	C/T	3.30322e-05	0.00406387	intron-variant, missense	RNF157, RNF157-AS1	GRCh38.p7	17:76152348	TGTTCAGCAGACTGA[C/T]ACTCACCAGGTAAGC	114804
rs143082385	snp	A/G	4.9534e-05	0.0049764	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76158399	GTCAATTACCTCTCC[A/G]AGATGCTGAACCGAC	114804
rs143118765	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76197061	AACCCAACCTAAACC[G/T]GTTGATATCAGATGT	114804
rs143174729	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76182113	CTTGGATACAACATC[C/T]TCCTGGGACTGGGCT	114804
rs143222036	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76166738	AGAACCTCTAACCTA[C/T]AGATTTTTTTTTTCT	114804
rs143241709	snp	C/T	0.0232847	0.105357	intron-variant	RNF157	GRCh38.p7	17:76205066	TGCTGGGATTAGAGG[C/T]GTGAGCCACCATGCC	114804
rs143418770	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76208070	AGAGGCATGCACCAC[C/T]ACGCCTGGCTAATTT	114804
rs143498211	snp	C/T	0.0126979	0.078662	intron-variant	RNF157	GRCh38.p7	17:76172268	GCAGTGAGCTGAGAT[C/T]GTGCCACTGTACTGC	114804
rs143525474	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76158641	CATTATGTTTCCCAG[A/G]CTGGGCTGGGACTCC	114804
rs143531209	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76232057	AAGTTAAATCATGTT[G/T]TATAGCATGTATCAG	114804
rs143543406	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76203593	GAGTAGTTGGGATTA[C/T]GGGAACCCGCCATCA	114804
rs143592692	snp	A/C	0.0130921	0.0798413	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149786	CACCTGTAATCTCAG[A/C]ACTTTGGGGGGCCGA	114804
rs143602618	snp	G/T	0.00438332	0.0466095	intron-variant	RNF157	GRCh38.p7	17:76220492	CATTTATCTTGCCTT[G/T]CCTACATGAACTGTA	114804
rs143620505	snp	A/G	0.0150606	0.0854603	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149895	AAAAATTAGCCGGGC[A/G]TGGTGGCGGGCGCCT	114804
rs143649446	in-del	-/AAAATAAATAAA	0.0452528	0.143452	intron-variant	RNF157	GRCh38.p7	17:76186940	ATGAGACTCCGACTC[-/AAAATAAATAAA]TAAATAAATAAATAA	114804
rs143655955	snp	C/G	0.00676609	0.0577691	intron-variant	RNF157	GRCh38.p7	17:76188235	GGTGACTTACGTTCT[C/G]TTGTACTGCATCCCA	114804
rs143673096	snp	G/T	1.65828e-05	0.00287943	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76159550	AGATACTACTTCATA[G/T]CCTGGTGGAATATTC	114804
rs143674895	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241843	CCAATTCCTGACCTC[C/T]GCCCCCCAAAGCGCT	114804
rs143679410	snp	C/T	0.0429648	0.14013	intron-variant	RNF157	GRCh38.p7	17:76170931	GGAGTCTCACTCTGT[C/T]GCCCAGGCTGAAGTG	114804
rs143725203	snp	A/G	6.59968e-05	0.00574404	synonymous-codon, intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152452	CATACCTAGAAATGC[A/G]CACGTCCTCTGGCCT	114804
rs143735833	snp	A/G	0.00119737	0.0244387	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153173	GGGCTAGGGAATGTC[A/G]GTGAAACAACCTGGC	114804
rs143754066	snp	C/T	0.0267878	0.112589	intron-variant	RNF157	GRCh38.p7	17:76185768	GCCACCGCGCCCGGC[C/T]GAGATTACTCCTTTC	114804
rs143758012	snp	G/T	4.56361e-05	0.0047766	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155686	TCAGTGCTGATCTGG[G/T]AGGATGCCATGGACA	114804
rs143765215	snp	A/C	1.65211e-05	0.00287407	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76158471	CTCATCTTCCTCTTC[A/C]TGCAGCACGGAAGAG	114804
rs143768069	snp	A/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76173324	AAAATATAGCAATAA[A/T]ATAAAGGATTTGATA	114804
rs143845436	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76227529	TTCTTTTCATTTTAT[A/G]GAAGAGGAAACTAAT	114804
rs143860846	in-del	-/T	0.0170251	0.090679	intron-variant	RNF157	GRCh38.p7	17:76218074	ATTTAACGTTATGTG[-/T]TTTTTTTGCCACAAT	114804
rs143873675	snp	A/G	0.00478085	0.0486577	intron-variant	RNF157	GRCh38.p7	17:76171968	GATGAGAGAAACCAA[A/G]TGGACAGAGTAGCTG	114804
rs143901148	snp	A/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144382	GCGCGATCTCGGCTC[A/T]CTGCAAGCTCCGCCT	114804
rs143918835	snp	A/G	0.0569829	0.158885	intron-variant	RNF157	GRCh38.p7	17:76190688	ACTTTGGGAGGCCGA[A/G]ACGGGTGGATCACGA	114804
rs143923158	snp	C/T	0.00517822	0.0506191	intron-variant	RNF157	GRCh38.p7	17:76222459	ATGTTACGTGAACTT[C/T]GCCTCAATTTTAAAA	114804
rs144025011	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76161234	AAATAATCGTCCCAT[C/T]GTTTCTGCCTGGGGG	114804
rs144025116	snp	C/G	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76206481	AAAGACCTTCAGAAG[C/G]CCAGTTTACTACTTA	114804
rs144042581	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76175666	CAAAATAAATGACTT[C/T]GGGATTAAAATTTTT	114804
rs144081814	snp	A/G	0.00438332	0.0466095	intron-variant	RNF157	GRCh38.p7	17:76204135	GTCTTTCCAGCCTCA[A/G]CTCCAACCAGCATCC	114804
rs144140755	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76207640	CTGCAAAGAGGAGTC[A/G]TTCTTGCCGCATGCT	114804
rs144159568	snp	A/C	0.00438332	0.0466095	intron-variant	RNF157	GRCh38.p7	17:76162110	AGTAATAATTACGAA[A/C]AAAATCTGCATTGAC	114804
rs144216891	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76193959	CTTCTCTGGGGTACA[C/T]GTCCACAAACGGGAC	114804
rs144270104	snp	C/T	0.0111196	0.0737302	intron-variant	RNF157	GRCh38.p7	17:76204575	AATCATGTTCTCTTT[C/T]TTTGCCACAAAGCTC	114804
rs144273940	snp	A/C	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154193	TGAGCAGCGCCACCA[A/C]GTCATACCGGTACCC	114804
rs144334591	snp	C/T	5.68537e-05	0.00533138	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76173706	TGGGAACTTACTTGA[C/T]GAGCCTCAGTGTGTC	114804
rs144349041	snp	A/T	0.00755907	0.0610114	intron-variant	RNF157	GRCh38.p7	17:76237993	GGAGACTGAGGCGGG[A/T]GAATTGCTTGAACCC	114804
rs144357799	snp	C/T	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151805	CTAACTCGACCTCTC[C/T]GTTGGGATCCAAATC	114804
rs144408647	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76198820	GCATACCAGGCCCCT[C/T]GGTCCAGGCCTGGCA	114804
rs144424197	snp	C/T	0.00993419	0.0697739	intron-variant	RNF157	GRCh38.p7	17:76168580	GGTCCCTTGGACTTG[C/T]TCCCATCTGTACTTG	114804
rs144444071	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76207416	TGACAGGGCAAGTCC[C/T]TATCTCTAGGGGAAA	114804
rs144488826	snp	A/G	0.0174175	0.0916809	intron-variant	RNF157	GRCh38.p7	17:76226927	CCGCTGGGGGGTGCC[A/G]CTGCAGAGCCTGGTG	114804
rs144491104	snp	C/T	0.000644048	0.0179335	synonymous-codon, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156280	AATAGCTCCAGATGA[C/T]GACAAGGTGAGATTC	114804
rs144524285	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76155128	TCTCACTGATCTAGG[A/C]ATGTCCCCTAGGAAG	114804
rs144531006	snp	A/C/T	0.000148292	0.00860963	synonymous-codon, missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161595	AAAGCTGGTTGGGGA[A/C/T]AAGGGGCCCAATTTT	114804
rs144558754	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76210898	CAACCTCCACTTCCC[A/G]GGTTCAAGCGATTCT	114804
rs144570726	snp	A/C	0.00597247	0.0543191	intron-variant	RNF157	GRCh38.p7	17:76179725	TCTTATTTCAACCTA[A/C]AACCAGAGATCTCAC	114804
rs144604959	snp	C/T			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76214286	GAGAGAATCCCCACA[C/T]ATTTTGCTGACCAGA	114804
rs144649227	snp	A/G	0.0111196	0.0737302	intron-variant	RNF157	GRCh38.p7	17:76178195	GAGCTGTGGCCCGTC[A/G]GGGAGCCCAGACCTG	114804
rs144658637	snp	A/G	0.00636936	0.0560724	intron-variant	RNF157	GRCh38.p7	17:76176238	TCAAAGAGATTAAAT[A/G]TATGGATATTTTTTT	114804
rs144729370	snp	C/T	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76188254	TACTGCATCCCACGG[C/T]CTCCTACCTGGGATC	114804
rs144749838	snp	A/G	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76230333	TGCTCCAGAATTCCA[A/G]TTTCTGTCAATGGTA	114804
rs144766153	snp	C/T	0.0166325	0.0896639	intron-variant	RNF157	GRCh38.p7	17:76160654	TAGCTTTTCCTCTGA[C/T]ACACACATTGTAAAT	114804
rs144817986	snp	C/G	0.030665	0.119967	intron-variant	RNF157	GRCh38.p7	17:76223211	TTTTTTTTTTGAGAC[C/G]TAGTCTCACTCTGTC	114804
rs144820493	snp	C/T	0.00914312	0.0669923	intron-variant	RNF157	GRCh38.p7	17:76165770	GTGGCCTCCGCCTCC[C/T]GGTTCCAGCAATTCT	114804
rs144858846	snp	A/G	0.248755	0.249997	intron-variant	RNF157	GRCh38.p7	17:76233200	GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCT	114804
rs144926225	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76192506	CAGAAATAGATGTCT[A/G]TAGAATGAATACACG	114804
rs144952082	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76237442	TGCCACTTGCTTTGT[C/T]CCACTGTTAGTACTC	114804
rs144982425	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF157	GRCh38.p7	17:76155919	CTTTATATTTTAGAG[C/T]TCAGAACTCAGCCTT	114804
rs144993750	snp	G/T	0.00318978	0.0398085	intron-variant	RNF157	GRCh38.p7	17:76232776	CTGCCTTTTCTATTT[G/T]AGTTATCCTAATTCT	114804
rs145067370	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76195474	TGAAAAGCGGTTAGC[A/G]GTATCTACTACAGCA	114804
rs145080165	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76182451	ACACACGCATTTAGT[C/G]TGTGTGTGTGTGTGT	114804
rs145088345	in-del	-/AAACAAAT	0.455263	0.142713	intron-variant	RNF157	GRCh38.p7	17:76189835	GAGGAGAACACAAAC[-/AAACAAAT]AAAAACAACTGAAGG	114804
rs145120669	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76163792	CCTGGAGAACCAGGC[C/T]TTCCCCCATGAGGCA	114804
rs145132110	snp	A/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76181018	GTTAAACAAACTGAC[A/T]TTCTACAGATAAAGA	114804
rs145139083	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76235777	GCTTTGGGACCCCGA[A/G]GTGGGAGGACTGCTT	114804
rs145144263	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76157571	CTTTTCCATCTCTGA[C/T]ACAGCAATTTATCGT	114804
rs145150447	snp	A/C/T	0.00234035	0.0341277	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76173781	GGGGAGGTGGGGCGG[A/C/T]GTAAGGAAACTGTGT	114804
rs145161063	in-del	-/GAG			intron-variant	RNF157	GRCh38.p7	17:76230860	AAAAAAAAAAAAAAA[-/GAG]AGAGAGAGAGAGAGA	114804
rs145194609	snp	G/T	0.0023933	0.0345097	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146066	CCCCCACATGAGGAG[G/T]GCCAGCGCCTGTCTG	114804
rs145212940	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76181320	TATGCTTAGATGGCA[C/G]TATGTACAAAATCAT	114804
rs145254594	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76182845	TATATATGATATATA[G/T]GATATATAGGATATA	114804
rs145256379	snp	A/G	0.0142736	0.0832652	intron-variant	RNF157	GRCh38.p7	17:76178498	TCCCTTGGAGGCGTG[A/G]GATATAGGCTGGTAG	114804
rs145261148	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145390	TTACAGGAGCCAGAC[C/T]TTTGGCCAAATCCAG	114804
rs145287725	snp	C/T	0.0111196	0.0737302	intron-variant	RNF157	GRCh38.p7	17:76204577	TCATGTTCTCTTTTT[C/T]TGCCACAAAGCTCTA	114804
rs145332038	snp	A/C/G	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76186669	TGGGCCGGGGGGGCA[A/C/G]TGGCTCACGCCTGTA	114804
rs145387754	snp	C/T	0.00557542	0.0525036	intron-variant	RNF157	GRCh38.p7	17:76211355	CTTCCCAGTGTAACA[C/T]TGAAGCAACCTGCCC	114804
rs145396146	snp	A/G	0.00716266	0.059414	intron-variant, upstream-variant-2KB, downstream-variant-500B	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76141968	CGCACTCACTCCTCT[A/G]GAGACAGCTGATGAA	114804
rs145409044	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76167859	TTAAAATTTACCTTT[-/A]AAAAAATTAGCAATA	114804

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