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
rs145492433	in-del	-/AG	0.147991	0.228242	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150623	GGGCACAGCTAAGAA[-/AG]AGACATCATCTTCAC	114804
rs145493013	snp	C/T	0.0111196	0.0737302	intron-variant	RNF157	GRCh38.p7	17:76227643	AGCAGTTTGGGAGGC[C/T]GAGGTGGGCGGATCA	114804
rs145563025	snp	C/T	0.00801667	0.0628018	missense, upstream-variant-2KB, nc-transcript-variant	RNF157	GRCh38.p7	17:76212479	TGGCTGGCAAAATAG[C/T]TTCCTAGAGAGGAAC	114804
rs145613557	snp	A/G	3.30573e-05	0.00406541	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76158480	CTCTTCATGCAGCAC[A/G]GAAGAGTTTTGGGAA	114804
rs145639727	snp	G/T	0.00835141	0.0640778	intron-variant	RNF157	GRCh38.p7	17:76198655	TCAGTTGGACAACTG[G/T]TTACCCTGTATCCGT	114804
rs145686252	in-del	-/CTCT			intron-variant	RNF157	GRCh38.p7	17:76190164	CAGGCTAACTGCTTG[-/CTCT]CTCTTTTTTTTTTTT	114804
rs145718764	snp	C/G/T	0.0131032	0.0799785	intron-variant	RNF157	GRCh38.p7	17:76208861	CACCTGTAATCCCAG[C/G/T]TAGTCAGGAGGCTGA	114804
rs145777373	snp	A/C	0.000399281	0.0141238			GRCh38.p7	17:76170540	AGAGTCATCTGCCTG[A/C]CTTTGGCCAAGGTGT	114804
rs145916370	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76225952	TGTCTTGTTTTGCTC[A/C]ATTTTTTTCAGCTTC	114804
rs145918035	snp	C/T	0.0107246	0.0724382	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153416	CCAACACTTCCCAAG[C/T]GATGGCCAGCGCTAA	114804
rs145929170	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76173915	AACTCTCCTAATTAA[C/G]TGAGGAAACTGAAAC	114804
rs146038844	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76207696	TCTTTCTTGCTCCCC[C/T]GTAACCTAACACTCA	114804
rs146062036	snp	A/T	0.000382864	0.0138306	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159573	GAATATTCTCTGAGG[A/T]CTAGGGGAATCAGAG	114804
rs146116569	snp	A/C/G	0.00398731	0.0445001	intron-variant	RNF157	GRCh38.p7	17:76156826	TCCGATCCCAGCCCC[A/C/G]ACCTGTCAGGCATCT	114804
rs146145197	snp	C/T	0.00478085	0.0486577	intron-variant	RNF157	GRCh38.p7	17:76228896	GCCATTGGACTCCAG[C/T]CTGGGCGACAGAGTG	114804
rs146151105	snp	C/T	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76230561	AAGGAGATACTGAGC[C/T]GGGCATGGTGGCTCA	114804
rs146162114	snp	A/G	0.0142736	0.0832652	intron-variant	RNF157	GRCh38.p7	17:76227222	GCTTCCTGGGTTCAA[A/G]AGATTCTCCTGCCTC	114804
rs146163483	snp	C/T	1.65124e-05	0.00287331	intron-variant	RNF157	GRCh38.p7	17:76155233	GGAAGGGGGCACCAC[C/T]CCGTGCTGTTGGGGT	114804
rs146163864	snp	C/T	0.000496073	0.0157414	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167076	TGCTGACACACTCCT[C/T]GCTTGTACTGCACAG	114804
rs146194120	in-del	-/AA	0.493925	0.054776	intron-variant	RNF157	GRCh38.p7	17:76215541	GATTTATAGCAAACT[-/AA]AAAAAAAAAAAAAAT	114804
rs146245620	in-del	-/AGAG			intron-variant	RNF157	GRCh38.p7	17:76230895	AAGAGAAAGAGAGAA[-/AGAG]AGAGAGAGAGACTTT	114804
rs146304492	snp	A/G	0.00279162	0.0372561	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154542	GATTAGATCCGAGCC[A/G]CATTACCCATATATG	114804
rs146324319	snp	C/T	1.64749e-05	0.00287005	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167760	GGACTTTAGCTTTAC[C/T]GGCCTCTTCTCCAGG	114804
rs146393106	snp	C/T	0.00517822	0.0506191	intron-variant	RNF157	GRCh38.p7	17:76194367	TCGCATAGAACACCA[C/T]GCACTCAGCCACCAT	114804
rs146403963	snp	C/G	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76191573	GCCACTGCACTCCAG[C/G]CTGGGCGACAGAGCA	114804
rs146439206	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76218384	AGTGGCTCACGCCTG[C/T]AATCCCAGTACTTTG	114804
rs146450711	snp	A/T	0.0154538	0.0865337	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76148254	AAAAGATCCAAATTA[A/T]CTTTGCCTTTTTTTT	114804
rs146490150	snp	A/G	0.00517822	0.0506191	intron-variant	RNF157	GRCh38.p7	17:76204391	CTCTGGTCCTCTCTC[A/G]TAGAACCTATCACAG	114804
rs146564184	snp	G/T	0.0115144	0.0749975	intron-variant	RNF157	GRCh38.p7	17:76236737	TGTTTATCAACAGGA[G/T]ACTATGTAAAAAAAA	114804
rs146564714	snp	C/T	0.0138799	0.0821421	intron-variant	RNF157	GRCh38.p7	17:76165817	AAGTATCTGGGATTA[C/T]ACGCATGAGCCACCA	114804
rs146610644	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76224160	CAACTATTTGTTCCT[C/T]ATAATGTGAACAAAA	114804
rs146613469	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151892	CCCTAGCCTCTGAAA[C/T]GCTGGCTTTCACATT	114804
rs146683833	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76181091	AGCTAATGAGCAGCA[A/G]AACCACAATTTGAAC	114804
rs146709446	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76171225	TTGGAGTCTCACTCT[A/G]TCACCCAGAGTGGAG	114804
rs146731500	snp	A/G	0.0356815	0.128715	intron-variant	RNF157	GRCh38.p7	17:76169725	GCTGGGATTATAGGC[A/G]TGTGCCACCAGGCCC	114804
rs146804805	snp	C/T	0.00676609	0.0577691	intron-variant	RNF157	GRCh38.p7	17:76200922	CCTCCCCATGCTTAC[C/T]CTGGTTTTCTGTCTT	114804
rs146843972	snp	C/T	0.000908257	0.0212909	synonymous-codon, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156241	AGTGGATGACAGAGG[C/T]GTCCCTGTGCAAGAC	114804
rs146854851	snp	C/T	0.0126979	0.078662	intron-variant	RNF157	GRCh38.p7	17:76186399	GTAATCCCAGCTACT[C/T]AGGAGGCTGAGGCAG	114804
rs146877169	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151245	GGCAGTGTCTTTAGA[A/T]CAAACTAAATAGAAA	114804
rs146952775	snp	A/C/G	3.30181e-05	0.00406303	missense, stop-gained, nc-transcript-variant	RNF157	GRCh38.p7	17:76166509	GAGGGTAAACTTCTC[A/C/G]GTCTAAATCAAAGCC	114804
rs146974333	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76188104	CAAGTGAACTACTTT[A/C]TTTGGCTTTTATGAA	114804
rs146984404	snp	A/G	0.0123036	0.0774623	intron-variant	RNF157	GRCh38.p7	17:76229746	TACTTAGAATGGAGA[A/G]TGGCACACTAAGGGT	114804
rs147003862	snp	G/T	0.00835141	0.0640778	intron-variant	RNF157	GRCh38.p7	17:76193301	ATTAGTGATCCTTAG[G/T]GATTAGCATTAGTGA	114804
rs147079862	snp	A/G	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76206090	TTTTTAAAAAGCCAG[A/G]CATGGTGGGGCGTGC	114804
rs147109329	snp	A/G	0.0134861	0.0810011	intron-variant	RNF157	GRCh38.p7	17:76209516	AGCTCATCAGCTATC[A/G]TTACTGCTAGTGTAT	114804
rs147166179	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76161394	GTTGGTTTTAACGCA[C/T]GCTCTCAGCCGGCTT	114804
rs147193534	snp	C/G	0.00755907	0.0610114	intron-variant	RNF157	GRCh38.p7	17:76221801	AGGTATAATGTGTCC[C/G]ACATATGTCCTTACA	114804
rs147195902	snp	A/G	0.0185938	0.0946107	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149907	GGCGTGGTGGCGGGC[A/G]CCTGTAATCCCAGCT	114804
rs147209290	snp	A/G	3.3083e-05	0.00406699	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76158496	GAAGAGTTTTGGGAA[A/G]TGGATCTGTAGGAGT	114804
rs147269913	snp	A/C	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76226540	GAACTCCTTCAAATC[A/C]ATTTTCTCCAACATC	114804
rs147279638	snp	G/T	0.0119091	0.0762411	intron-variant	RNF157	GRCh38.p7	17:76222721	GAGAGATGCAAGGTT[G/T]GAACCGAAGGTCTGG	114804
rs147290865	in-del	-/ATAA			intron-variant	RNF157	GRCh38.p7	17:76205731	CCATCTCTAAATAAA[-/ATAA]TAAATAAATAAATAA	114804
rs147375391	snp	C/T	0.00318978	0.0398085	intron-variant	RNF157	GRCh38.p7	17:76199202	TATCTTCTCAACTAG[C/T]ACAGAGACCAGATTA	114804
rs147385318	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76238431	AAAACTGGTAGAGAG[A/G]AGAGGATTATTTATT	114804
rs147405365	snp	C/T	0.0295035	0.117819	intron-variant	RNF157	GRCh38.p7	17:76183125	TATTTTTAGTAGAGA[C/T]AGGGTTTCTCCATGT	114804
rs147481694	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76215428	TGCAGCGAGCTATGA[C/G/T]TGCCACTGCACTCCA	114804
rs147483199	snp	A/G	0.00597247	0.0543191	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145442	CCCAGGAGCCGGCAC[A/G]GAAGGAGCAGGATGC	114804
rs147510530	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76202376	TCCTTTGCCTCAACT[C/T]ACACTGCTGCAATTC	114804
rs147567353	snp	C/T	0.00502839	0.049889	intron-variant, downstream-variant-500B	RNF157	GRCh38.p7	17:76156196	CATGCAGCCACTCCC[C/T]GCTCCTTATGTACCT	114804
rs147568850	snp	C/T	0.0126979	0.078662	intron-variant	RNF157	GRCh38.p7	17:76200135	TAGTCCCAGCCACTC[C/T]GGAGGCTGAGGCAGG	114804
rs147597063	snp	A/G	0.00318978	0.0398085	intron-variant	RNF157	GRCh38.p7	17:76157996	CTTGGCTCCTGGACC[A/G]CTTTTTAAGAATGGC	114804
rs147629995	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76195539	CTTAACAGGTATGCA[C/T]ACATATACACAACAA	114804
rs147673464	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76172844	AGGGGTGGCGGGCAG[G/T]GGGAATGTATCAGAC	114804
rs147673544	snp	A/G	0.0134861	0.0810011	intron-variant	RNF157	GRCh38.p7	17:76216111	GGAAAAGTTAAAGAT[A/G]TTACACAGATGGATG	114804
rs147702513	snp	C/T	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76175986	CCCCTATACTTTAGG[C/T]TCTCCCTGTACACAC	114804
rs147734837	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76211926	GGCTTAACATTACGT[A/G]CCAGGCTTTGTTCTA	114804
rs147775350	snp	C/T	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76193065	CTCAAGTGATCCTCC[C/T]GCCTCGGCCTCCCAA	114804
rs147837934	snp	C/T	0.00636936	0.0560724	intron-variant	RNF157	GRCh38.p7	17:76231722	CTTGTCTTTATTTTA[C/T]CCAAAAGGCACAAAC	114804
rs147994869	snp	A/G	0.00755907	0.0610114	intron-variant	RNF157	GRCh38.p7	17:76173346	GATTTGATATTCTAA[A/G]TTCAAATTTCCCATT	114804
rs148039929	snp	A/G	0.0138799	0.0821421	intron-variant	RNF157	GRCh38.p7	17:76158763	CGAAACCCAAATCTT[A/G]AGTAGGACTAGGGAA	114804
rs148048582	snp	C/T	0.0138799	0.0821421	intron-variant	RNF157	GRCh38.p7	17:76178532	GAGCTGAGTGCAGCC[C/T]GTCAGGCCAAGTGGG	114804
rs148123698	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76189680	AGAAACTGCAGGAAA[C/T]GGTTTCCATCCCCAT	114804
rs148208221	snp	C/G	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76210200	GTAGACATCTGATAA[C/G]TATTACTTGACATAA	114804
rs148260771	snp	C/T	0.00755907	0.0610114	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144602	AAGGAGCTCTTGGCC[C/T]GGCGCGGTGGCTCAC	114804
rs148262270	snp	C/G	6.61813e-05	0.00575207	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167113	ACTGGAGGCTGTTGT[C/G]TTTGGGAATGTAGCT	114804
rs148283447	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76182378	CGAAAGATGAAATTG[A/C]CAGACCATGCCCAAA	114804
rs148302316	snp	A/G	0.0170251	0.090679	intron-variant	RNF157	GRCh38.p7	17:76166914	AAGCATGGCCTTCAA[A/G]CATCCGAGCAGCCCC	114804
rs148327378	snp	G/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76226619	ACCAACCCATCCACA[G/T]TCAGCCATTCGGAGG	114804
rs148364100	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76205105	TTCCTTCCTCCCTCC[C/T]TCGTTCCCTCCCTTC	114804
rs148396941	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76168698	GTAGAAGCTCATGTT[C/T]CCTGCACCTCAAGTC	114804
rs148410048	in-del	-/G			intron-variant	RNF157	GRCh38.p7	17:76211545	GACCAGGCAAACCTA[-/G]TTACATGACTTTGAG	114804
rs148472482	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76207562	AAGCCAGGAAGTCTA[C/T]GGCATTTATAGCTTA	114804
rs148503232	snp	A/G	0.000153988	0.00877328	missense, intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152456	CCTAGAAATGCGCAC[A/G]TCCTCTGGCCTGTAA	114804
rs148527018	snp	C/T	0.00438332	0.0466095	intron-variant, utr-variant-5-prime	RNF157	GRCh38.p7	17:76175769	TTCAAAAAAAAGATG[C/T]GTCTTTTCCCTTATT	114804
rs148554670	snp	G/T	0.029116	0.117091	intron-variant	RNF157	GRCh38.p7	17:76233267	CCATAATATTGAGTT[G/T]TAAGAGTTCTTAATA	114804
rs148735159	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76210991	TGTGTTTTTAATAGA[A/G]ATAGGGTTTCACCAT	114804
rs148755893	snp	A/G	0.000164772	0.00907517	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154362	CCTGTGAGTCTATGA[A/G]GCGGCAAAATGAGTA	114804
rs148764026	snp	A/G	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76198826	CAGGCCCCTTGGTCC[A/G]GGCCTGGCATCTCAG	114804
rs148808636	snp	A/T	0.00874735	0.0655527	intron-variant	RNF157	GRCh38.p7	17:76157266	CCTCCGCGCCCGGCC[A/T]GTCACACAGTCCTTC	114804
rs148810272	snp	A/G	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76173707	GGGAACTTACTTGAC[A/G]AGCCTCAGTGTGTCC	114804
rs148853520	snp	C/T	0.00279162	0.0372561	intron-variant, downstream-variant-500B	RNF157	GRCh38.p7	17:76155914	TGCTCCTTTATATTT[C/T]AGAGCTCAGAACTCA	114804
rs148857256	snp	A/G	0.000511032	0.0159767	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76166480	TCCTTCATCCACCAC[A/G]GCATGTACCACTAGA	114804
rs148876170	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76200344	TGTCTGTCTATTGAT[A/G]GATGAATGGATATAC	114804
rs148885417	snp	C/T	0.0103295	0.0711199	intron-variant	RNF157	GRCh38.p7	17:76221374	TCAAGCTGCTGAAAC[C/T]AGTTAACCACCAGCT	114804
rs148912222	snp	C/T	7.11313e-05	0.00596327	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76240177	GCGGGTAGCGGTACA[C/T]GGAATTAGACGGGAT	114804
rs148951821	in-del	-/TCTT	0.261608	0.24973	intron-variant	RNF157	GRCh38.p7	17:76225604	AATATACTGTAGGCA[-/TCTT]TCTATGTCTGTATTT	114804
rs149025811	snp	C/T	4.9755e-05	0.00498748	missense, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156314	CTTTCTGGAGTCACA[C/T]CACATTCCTGGGGGT	114804
rs149095038	snp	C/T	0.323671	0.238899	intron-variant	RNF157	GRCh38.p7	17:76171434	CCTCGGTGATCCGCC[C/T]GCCTTGGTCTCCCAA	114804
rs149113380	snp	G/T	0.00835141	0.0640778	intron-variant	RNF157	GRCh38.p7	17:76196393	AGAAGGGGAGCTTCT[G/T]GGGGTGCTGGCCATG	114804
rs149117768	snp	A/G	0.00318978	0.0398085	intron-variant	RNF157	GRCh38.p7	17:76225921	CCCTCTTCTTCTGGC[A/G]GTACCTAGTGGCTGC	114804
rs149135217	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76204673	TGACACATATGATAA[C/T]AGGGTTCAATTTACA	114804
rs149200112	snp	A/G	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76178010	CTGTTCCAAGGCTCA[A/G]TAAGGCTCCTCTTCG	114804
rs149210134	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146329	CTAGATGAGAGAATG[C/T]GAGCGTTGGTGAGTA	114804
rs149234707	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76207164	CTCACACCTGCAATC[C/T]CAACACTTTGGAAGG	114804
rs149239826	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76182838	TATATCCTATATATG[A/C]TATATAGGATATATA	114804
rs149254240	snp	A/G	0.00438332	0.0466095	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149321	CATGGGATGCAGCCC[A/G]GGCTCCATTTCCCAC	114804
rs149285969	snp	C/T	0.000131848	0.00811828	missense, intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152400	TGTCCAGTGCTTTCA[C/T]GCTTGCGATGTCAAA	114804
rs149306290	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153811	TGCCGGCCCGAGAGT[C/T]CTCTTTTACAGTAAT	114804
rs149380615	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76230328	GTTTCTGCTCCAGAA[C/T]TCCAATTTCTGTCAA	114804
rs149390437	in-del	-/T	0.499234	0.0195537	intron-variant	RNF157	GRCh38.p7	17:76230936	TTAAAAGATTTAATC[-/T]TTTTTTTTTTTTCTT	114804
rs149436074	snp	A/G	0.00795532	0.062565	intron-variant	RNF157	GRCh38.p7	17:76160410	TCTAGTTACACTCCT[A/G]TAAGTAATACAGAAG	114804
rs149446487	snp	A/C	0.00795532	0.062565	intron-variant	RNF157	GRCh38.p7	17:76171879	GCAGCCAGGCTGCCA[A/C]GGCAGAGGCTATGAC	114804
rs149468476	in-del	-/G			intron-variant	RNF157	GRCh38.p7	17:76207479	TGGTAGATCTGTGGT[-/G]CGAAGTACAGCTCAG	114804
rs149550205	snp	C/T	0.00016491	0.00907899	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76159403	GTCAAGAGGCGAGAT[C/T]GTCCTGACGGGGGGC	114804
rs149594746	snp	A/G	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76193742	GATCCGAAACAATCA[A/G]GAGCTGAGCGAGAAA	114804
rs149602225	snp	A/G	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76237990	TTGGGAGACTGAGGC[A/G]GGAGAATTGCTTGAA	114804
rs149677591	snp	A/G	8.24518e-05	0.00642021	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76165529	ACCCAGCAGTACATG[A/G]CAATGGCCAAAATAC	114804
rs149741851	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76200175	TGAACCTGGGAAGCG[C/G]AGCTTGCAGTGAGCC	114804
rs149779108	snp	A/G	0.00398564	0.0444627	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151103	CCTAACTGGCAGGAG[A/G]CTGGCCCCGTGGTCA	114804
rs149787194	in-del	-/GATATATAG	0.33693	0.2344	intron-variant	RNF157	GRCh38.p7	17:76182837	ATATATCCTATATAT[-/GATATATAG]GATATATAGGATATA	114804
rs149808654	snp	C/T	0.00835141	0.0640778	intron-variant	RNF157	GRCh38.p7	17:76206873	TATAGCTAACATTGC[C/T]GCATGCTGCTTTTTG	114804
rs149838003	snp	A/C	0.00170588	0.0291552	intron-variant	RNF157	GRCh38.p7	17:76155322	GCTGGCAGCCCCTGC[A/C]GAAGAGCACAGTTTT	114804
rs149900997	snp	A/G	0.0295035	0.117819	intron-variant	RNF157	GRCh38.p7	17:76231199	AGACAGGGTTTCACC[A/G]TGTTAGCCAGGATGG	114804
rs149920811	snp	A/G	0.00318978	0.0398085	intron-variant	RNF157	GRCh38.p7	17:76175542	GTTTCTCCTCCCCCA[A/G]CTTTCCTAGGCTGTC	114804
rs149951219	snp	G/T	0.00517822	0.0506191	intron-variant	RNF157	GRCh38.p7	17:76235602	TAGTTATTCGACAAA[G/T]ACTTATTATCCATGC	114804
rs149953414	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76162953	ATGGAAGGGCATGCA[C/T]TAAAATCTAGGCATT	114804
rs149971641	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76172837	ATCATCTAGGGGTGG[C/T]GGGCAGTGGGAATGT	114804
rs149995036	snp	A/C	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76185230	CTTGACTTCCAGGCC[A/C]CCCCAGATAGGAAGC	114804
rs150048101	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76192272	AAAGTTCAAGCACTT[A/G]GTGGCACTTTTCGAG	114804
rs150078595	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76198895	CCACACCTGCTTATG[A/C]TGAATCACCTGCAGT	114804
rs150080490	snp	A/C	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76148906	CTGACTACCCCAGGG[A/C]CTTCATAGAACTATC	114804
rs150105284	snp	C/G	0.000153988	0.00877328	missense, intron-variant, utr-variant-3-prime, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145275	CAGGGCCTCGTCTCA[C/G]AGTCCTCCAGGCTGC	114804
rs150143644	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76193666	GTGAGAGTTAAGCAC[A/G]TTCTCCTTTTGTCTG	114804
rs150150989	snp	C/T	8.23676e-05	0.00641693	missense, utr-variant-5-prime, nc-transcript-variant	RNF157	GRCh38.p7	17:76212396	CCAGAAAGTTCAGAT[C/T]GCTGTTCTCTCCAAA	114804
rs150205076	snp	C/T	6.58989e-05	0.00573978	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76167677	ATTCTGGAACTCTTC[C/T]GTGGCCTGGTAATAG	114804
rs150213830	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76197948	TAGGCTTGCAAATAG[C/T]CCTCTCCCTTGAAGA	114804
rs150214389	snp	A/G	0.00318978	0.0398085	intron-variant	RNF157	GRCh38.p7	17:76170415	TGTATTTCTTGTAGA[A/G]ACAGGGCTTTACCAT	114804
rs150232473	snp	A/G	0.0158469	0.0875917	utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142704	TCCCAGGTGAGGTGG[A/G]CAGGACCCTAACTCC	114804
rs150269598	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76201773	GCCATCTCAGTGGAC[A/G]CAGATCTATCTAATT	114804
rs150300311	snp	C/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76225444	ACTATTCACAATTGG[C/G]TGTGGCCTTCCAGAT	114804
rs150308331	snp	A/T	0.0126979	0.078662	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152773	CGAGCAGAGCTGGGC[A/T]GAGGCCAGGCTGGTG	114804
rs150311433	in-del	-/TAAATAAA	0.194058	0.243661	intron-variant	RNF157	GRCh38.p7	17:76205724	GCAAGACTCCATCTC[-/TAAATAAA]TAAATAAATAAATAA	114804
rs150428824	snp	C/G	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76232339	GCTGCAGGGAGCTAT[C/G]ATCGCACCACTGCAC	114804
rs150448014	snp	C/T	0.0138799	0.0821421	intron-variant	RNF157	GRCh38.p7	17:76177825	TGTCCATAAGACCAG[C/T]TGCAGAGAGGAGCTA	114804
rs150457856	snp	A/G	0.00517822	0.0506191	intron-variant	RNF157	GRCh38.p7	17:76218257	CAGACTTTTCAACAG[A/G]AACACTTTATGTCAG	114804
rs150482547	snp	A/G	0.00676609	0.0577691	intron-variant	RNF157	GRCh38.p7	17:76237897	AGACTTGCCTGGCCA[A/G]TATGGTGAAACCCCA	114804
rs150535542	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76206525	AAACCAGTGAAGAGG[A/C]CGGCCAAGGTGGCTC	114804
rs150578741	snp	G/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76239748	TCCCTCGCGGCCCTC[G/T]GACCCCGCGAGGCAG	114804
rs150605508	snp	C/T	0.00398564	0.0444627	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150997	CATTTGGCAAAATGA[C/T]GTGAAACACAAATGG	114804
rs150633713	snp	A/C	0.00726163	0.0598171	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76155610	CTGGGGGGAAGAGAG[A/C]GCCTCTCCCTCCTCT	114804
rs150672751	snp	A/G	0.0240643	0.107019	intron-variant	RNF157	GRCh38.p7	17:76194742	AAGAGCAGGCCGGGC[A/G]CGGTGGCTCACACCT	114804
rs150691176	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76182837	ATATATCCTATATAT[C/G]ATATATAGGATATAT	114804
rs150762833	snp	C/T	0.00597247	0.0543191	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76144810	GATCCTCCAGCCCTA[C/T]CCCAAACTGCAGGTT	114804
rs150807809	snp	A/G	0.00795532	0.062565	intron-variant	RNF157	GRCh38.p7	17:76214853	TGACAGGATATGATG[A/G]AACTGAGAAGTCACC	114804
rs150859932	snp	C/T	0.0197687	0.0974348	intron-variant	RNF157	GRCh38.p7	17:76185164	AGTCCCACTCTGTCA[C/T]TAAACACACCTACAT	114804
rs150879466	snp	A/G	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76157349	CAGGCTGCACACTGC[A/G]GTCGGGTGGGCCTTT	114804
rs150883891	snp	A/G	0.00478085	0.0486577	intron-variant	RNF157	GRCh38.p7	17:76231128	TCAGCCTCCCAAGCA[A/G]CTGTGACTACAGGCA	114804
rs150921126	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76163126	GGCTAATGGTGTGTA[C/T]CCCACACCATGAAGC	114804
rs150935683	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76228544	TCTCCACTGGCTTCT[A/T]ACTTACCTCATCCTA	114804
rs150965053	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76186706	GCACTTTGGGAGGCC[A/G]AGGCGGGCAGATAAC	114804
rs150979185	snp	A/T	0.00874735	0.0655527	intron-variant	RNF157	GRCh38.p7	17:76232110	GAACATGGCCAGGCG[A/T]GTTGTCTCATGCCTG	114804
rs151007367	snp	G/T	0.0138799	0.0821421	intron-variant	RNF157	GRCh38.p7	17:76169063	ACCCTCTGGTTCTGA[G/T]AAGTTTTCTTAAATT	114804
rs151051506	snp	C/T	0.0197687	0.0974348	intron-variant	RNF157	GRCh38.p7	17:76208119	TAGAGATGAGGGTCT[C/T]GCTATGTTGCCCAGG	114804
rs151104674	snp	A/G/T	8.23953e-05	0.00641807	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76161601	GGTTGGGGACAAGGG[A/G/T]CCCAATTTTTTCCTC	114804
rs151114822	snp	C/G	0.00398564	0.0444627	intron-variant, upstream-variant-2KB, downstream-variant-500B	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142396	ACTCCAGATCCTCTT[C/G]AGTAAAAGTATTAAA	114804
rs151119417	in-del	-/TTTCTA	0.408188	0.193589	intron-variant	RNF157	GRCh38.p7	17:76224387	GACAATTAAACCCAT[-/TTTCTA]TTCTTCTACAATTCT	114804
rs151123200	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76180836	TTCGCATTATCGTGC[A/G]GCCATCACCGCCATC	114804
rs151144169	snp	C/T	0.00398564	0.0444627	intron-variant	RNF157	GRCh38.p7	17:76162425	ATCTGAAATGAGGAA[C/T]AAGAAAATACCCTTC	114804
rs151151678	snp	C/T	9.31424e-05	0.00682367	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76173732	GTGTCCTTTCGGATA[C/T]TGACCAGGCTTCTCA	114804
rs151200200	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76197233	TGTATAATATCCAGG[C/T]GATTTTGATGTCTTG	114804
rs151282409	snp	A/G	0.0103295	0.0711199	intron-variant	RNF157	GRCh38.p7	17:76211066	CACCTCGGCCTCCCA[A/G]AGTGCTGGGATTACA	114804
rs151334525	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146682	CACGCACACGTCACA[C/T]GGCAGAAACCGCTAG	114804
rs151338099	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76216787	TCCCAGCTACTCAAT[A/T]GGCTGAGGTGGGAGG	114804
rs180809367	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76238586	CCACATATGAAAGAG[C/T]GGTGAATACTTTCCT	114804
rs180821443	snp	C/T	0.0722614	0.17581	intron-variant	RNF157	GRCh38.p7	17:76185621	ACTACAGGCACCCGC[C/T]ACCACGCCCGGCTAA	114804
rs180837885	snp	C/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76220239	CCAGATAACAAGGAC[C/G]CTCTCTAAACCTACT	114804
rs180838335	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76210390	CGAGGTCAGATCGAG[A/G/T]CCATCCTGGCTAACA	114804
rs180845670	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76228242	CTTCACAGCATTTAG[A/T]GAAAGGCACACATCA	114804
rs180847609	snp	A/T	0	0	intron-variant	RNF157	GRCh38.p7	17:76162455	CTAAGACCTAACTGA[A/T]TTCAGAGTTTGGCAC	114804
rs180864412	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76201101	CCTTCCTCTACTTAG[A/G]AGTATTTCCACCTCT	114804
rs180883339	snp	G/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76235372	CTGGCTAATTTTTTT[G/T]TATTTTTAGTAGAGA	114804
rs180958781	snp	C/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76157803	GCTGCATAAACCTTT[C/G]TTAAGTGAGGTCTCT	114804
rs180966862	snp	A/C/T	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76197109	TGGGGGTGGATCACC[A/C/T]ACAGCCAGATGGCAA	114804
rs180968119	snp	A/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76169148	TTAGTTGGATGTCAG[A/T]CCTTCTAAATGGGTG	114804
rs180975355	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76215145	TCAGTTGCAATTTTT[A/G]TTGAAGATTTGTAGC	114804
rs180990382	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76205014	GGTCTTGATCTCTCC[C/T]GACCTCAAGTGATCC	114804
rs181012781	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76188535	TCTGAGACTAAAAAT[A/G]GCCAAGTTCCAACTT	114804
rs181024480	snp	C/T	0.00953873	0.0683987	intron-variant	RNF157	GRCh38.p7	17:76223439	GTGATCCATCCGCCT[C/T]GGCCTCCCAAAGTGC	114804
rs181077108	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76206565	AGCACTTTGGGAGGC[C/T]GAGGTGGGTGGATTG	114804
rs181085737	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76225204	AACAAAAATATTACA[A/T]GTTAGGTGCAATGGC	114804
rs181087683	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76148852	TGGGATTACAGGCGT[A/G]AGCCACTGTGCCCGG	114804
rs181147054	snp	C/T	0.00597247	0.0543191	intron-variant	RNF157	GRCh38.p7	17:76157233	GGCCTCCCAAAGTGC[C/T]GGGATTCCAGGCGTG	114804
rs181157260	snp	A/C	0.00438332	0.0466095	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149501	AGAAAGCTGAACTTA[A/C]AGCTGAGTGTGAAGA	114804
rs181162200	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76170888	AAAGAAATTTTTAAA[A/T]TTTTTTATTTATTTA	114804
rs181163368	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76179370	CTGCACTCCAGCTTG[G/T]GGGAGAGAGTGAGAC	114804
rs181164180	snp	C/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76188774	AAGAGGATTTAGTGA[C/G]TGGCTTCTAACGAAT	114804
rs181164608	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76195574	CATGTAATAATAGAA[C/T]GTTCATAGCAGCACT	114804
rs181177045	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76214508	CACACTTTAACTTGC[C/T]GCAAACATTATTGTT	114804
rs181304493	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76174233	AGGAGTTTAGGGACC[A/G]CAAATAAAAGAGGGC	114804
rs181312272	snp	A/C	0.0134861	0.0810011	intron-variant	RNF157	GRCh38.p7	17:76191611	GCCTCAAAAAAAAAA[A/C]AAAAAAAAAAACATT	114804
rs181322017	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144548	TCCTGATCTCATGAT[C/T]CACCCGCCTCGGCCT	114804
rs181586777	snp	A/T	0.00795532	0.062565	intron-variant	RNF157	GRCh38.p7	17:76207268	CTACAAAAAAAATTT[A/T]AAAAATTAGCCCAGT	114804
rs181592694	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76225856	CTCTTTTAGAGCCTC[A/G]TTCTTCTTTTCCAGC	114804
rs181687688	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76143060	GAGGACCAGCTCCTT[A/G]GATGGAGTATTTCTG	114804
rs181698812	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76214852	GTGACAGGATATGAT[A/G]GAACTGAGAAGTCAC	114804
rs181725461	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76229038	CTCAAATATTTACAA[C/T]AGTTTCCACCCCTCT	114804
rs181756947	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76235100	TTTAAAATAGGGTAG[C/T]GATAGTCCTCCAACT	114804
rs181779572	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76161700	ACAGGATTAAGAATG[A/T]ACAAGAGCCCAGACA	114804
rs181784356	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76184500	GGGGAGAGCAGCTTC[A/G]TATTTGCTTGAATGC	114804
rs181789521	snp	A/G	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76196379	AACAGGAAAGGAGCA[A/G]AAGGGGAGCTTCTGG	114804
rs181792008	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76200507	TCGTATGAGGTACCT[A/G]GAGTAGTCAAACTCA	114804
rs181795227	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76237855	GGAGGCCGAGGCAGG[C/T]GGATCACCTGAGAGG	114804
rs181796451	snp	C/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76154977	AAGGACAATATATTC[C/T]CAAGGCCAGGGGCTG	114804
rs181799645	snp	A/G	0.00597247	0.0543191	intron-variant	RNF157	GRCh38.p7	17:76219528	ATTATCTATAGGAGG[A/G]GGGAGGGAACGAAGT	114804
rs181800931	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76175064	ACATTATGGAATACG[C/T]ATCTCCATCCGTCCG	114804
rs181842080	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76174796	TCTGACTTAATGTAC[A/G]CAGTATAATTGCTTA	114804
rs181857403	snp	C/T	0.212728	0.247206	intron-variant	RNF157	GRCh38.p7	17:76210514	AGAATGGCGTGAACC[C/T]GGGAGGCAGAGCTTT	114804
rs181906291	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76157258	GGCGTGAGCCTCCGC[A/G]CCCGGCCAGTCACAC	114804
rs181908251	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76179884	TTAGCATTAGCAATC[A/G]TTTTCTCAGTTCATA	114804
rs181920437	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76193148	ACACAAGACTTTGGG[C/T]AAATAACTTAACATC	114804
rs181979844	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76229764	GCACACTAAGGGTAC[A/G]TATGGGTGCTTCTGT	114804
rs182088609	snp	A/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154553	AGCCACATTACCCAT[A/T]TATGCTCAGAATGGT	114804
rs182175065	snp	C/T	3.37861e-05	0.00410997	intron-variant	RNF157	GRCh38.p7	17:76155513	ATGCTACTTTGGACA[C/T]GTGCACAAAGAACAG	114804
rs182186420	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76175484	ATCAGGAGGCCTTGA[C/T]ATGGTAAAACTGAAA	114804
rs182194473	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146465	CCCTCCCTCCAGTGA[A/G]GCTAGGGCGCTCCTG	114804
rs182194844	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194084	GTTTATCAAGGTATA[A/G]TTTATATACAGTAAA	114804
rs182199641	snp	A/T	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76211422	ATTCAATCACTTCTG[A/T]TCTTTATTGTTAATT	114804
rs182202474	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76230099	GAAGAATGGACTGAT[A/G]TCTCATCTGCAGTGG	114804
rs182208160	snp	A/G	0.0142736	0.0832652	intron-variant	RNF157	GRCh38.p7	17:76211041	AGCTCCCAACCTCAG[A/G]TGATCTGTCCACCTC	114804
rs182259507	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144400	GCAAGCTCCGCCTCC[C/T]GGGTTCAGGCCATTC	114804
rs182302002	snp	A/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76236994	GGAGAACCAGGTGGA[A/T]GGACAACAGCGGTGA	114804
rs182309058	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150943	GTCTAGAGAACATAC[A/G]TGAGTTTAGAAAATA	114804
rs182350863	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76182763	CAGGCCTCGTCTCAT[A/G]TATATATATATATAT	114804
rs182360700	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76198494	GGAAAATCCACTAGC[C/T]GGCTGCGTCCTTTGG	114804
rs182369084	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76217647	AAAATCAGTGGTGGG[A/G]GAAAAGAACTCTACT	114804
rs182378729	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151661	AGGCACTCGGTGCTT[A/C]AAGTGTGATTAACAT	114804
rs182382754	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76172798	AATTTTTTCACCAGA[C/G]AATCAGACAGCCTTG	114804
rs182389558	snp	A/T	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76190178	GCTCTCTCTTTTTTT[A/T]TTTTTTTTGAAATAG	114804
rs182396516	snp	C/T	0	0	intron-variant	RNF157	GRCh38.p7	17:76208792	ACCTGTCCAACATGG[C/T]GAAACCCCATCTCTA	114804
rs182402914	snp	G/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76226863	AAGGTGTCTTTGTCG[G/T]TTACAGCAATGCTGC	114804
rs182471307	snp	A/G	0.0142736	0.0832652	intron-variant	RNF157	GRCh38.p7	17:76187270	CTCACCACAACCTCC[A/G]CCTCCCAGGTTCAAG	114804
rs182491441	snp	A/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76222916	TTTTTTTTGAGACAG[A/T]GTCTCGCTCTGTTGC	114804
rs182630985	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76208115	TTTGTAGAGATGAGG[A/G]TCTCGCTATGTTGCC	114804
rs182718701	snp	A/G	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76172452	CAAAATTAACCGGGC[A/G]TGGTGATGCATGCCT	114804
rs182738295	snp	C/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76203126	CTCCCAAGCGGCTGG[C/G]ATTACAGGCATGCAC	114804
rs182791971	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76197431	AATTTGGAAGGCTGA[A/G]GCGGGAAGATCACTT	114804
rs182823930	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB	RNF157	GRCh38.p7	17:76242009	TGTCATTTATATTGG[C/T]TGCTGCTAACGAAGG	114804
rs182832312	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76235746	GGGTACGGTAGATCA[C/G]TTCTGTAATCCCACT	114804
rs182842097	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76166821	AGGGAATGGAAAAAT[G/T]AACAAAGTTAGGTAT	114804
rs182866842	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76158683	GATCCTCTTGTTGAC[A/G]CTTTAACAGAGGAGG	114804
rs182898478	snp	A/G	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76189639	AGAGAACTAAAACAC[A/G]AAAAGGGGGCACGGA	114804
rs182920753	snp	C/G/T			intron-variant	RNF157	GRCh38.p7	17:76226401	TTGGGTTCACCATCT[C/G/T]GGGGGGCACCTTATT	114804
rs183020925	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76159017	GGTTCCTTCAGTCTT[C/T]GGACTAAGCAATGCT	114804
rs183031822	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76182033	GGACACAGTGAAGAG[C/T]CAAGCAAACCTCTCT	114804
rs183037978	snp	A/G	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76198245	CCTGAGGGTGTTGGA[A/G]TACAAAGTTGGATGA	114804
rs183074005	snp	A/G	0.00438332	0.0466095	intron-variant	RNF157	GRCh38.p7	17:76181341	ACAAAATCATACCAC[A/G]CACCACACTCCTTTC	114804
rs183084708	snp	C/T	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76221045	AGAATTACTTGAACT[C/T]AGTAGGTCAAGGCTG	114804
rs183087106	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76215827	ACTGAAAGTCACCCA[C/T]TAAAACTTAAAAAGA	114804
rs183137823	snp	C/G			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145582	ACAGTCACTGCCACT[C/G]TGGCTCCCGGACAGG	114804
rs183152859	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76163987	ATTAACCTAAAAGAA[C/T]GAACAGTGTAGAATT	114804
rs183159664	snp	A/G	0.00438332	0.0466095	intron-variant	RNF157	GRCh38.p7	17:76185867	CACAAATTAGAATAC[A/G]CTTTTAAGCAGCAGG	114804
rs183165395	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76201785	GACGCAGATCTATCT[A/C]ATTTTTGCTGAATAA	114804
rs183243657	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76202220	CTTTAGGCCTGTAGG[A/G]CAGTTAAGTGCCAGG	114804
rs183248386	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76221406	ATAGGGAATAAAACA[A/G]AACATGATTAATGAG	114804
rs183260519	snp	A/G	0.494733	0.0510469	upstream-variant-2KB	RNF157	GRCh38.p7	17:76240712	GGACTCGCGACGGGG[A/G]CGGGGGCGCGGCCGG	114804
rs183330575	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76216635	TATTCAGTCAGTAGA[A/G]TATTATGAAGCCTTT	114804
rs183377822	snp	A/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150012	CACTCCAGGCTGGGC[A/G]ACAGAGCGAGACTCT	114804
rs183407978	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76189351	AAATTAATTCAGCAA[A/G]AGAAATGCAGAGATG	114804
rs183468209	snp	A/C	0.00597247	0.0543191	intron-variant	RNF157	GRCh38.p7	17:76239761	TCGGACCCCGCGAGG[A/C]AGGTAGGCTTTGGGC	114804
rs183487584	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76176867	AGCAGCTTCCGCTTC[A/G]GGCACCTGGCCATTG	114804
rs183632897	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76171783	AAGCAAGCATCTGTG[C/G]ACCTGGGAGGCAAAC	114804
rs183659098	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76236185	GAATTTCTGTAGTAG[A/G]TTTACTTCTTAAAGA	114804
rs183698837	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76231276	TGCTCAGATTACAGG[C/G]GTGAGCCACCGTGCC	114804
rs183709249	snp	G/T	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76179349	CAGTGAGCTATGATA[G/T]CATCACTGCACTCCA	114804
rs183712883	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76195466	AATCACTTTGAAAAG[C/T]GGTTAGCGGTATCTA	114804
rs183722409	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76214161	GGCAGTCTTGTGAGA[C/T]TGCACCCTCAACCTG	114804
rs183737274	snp	C/T	0.0166325	0.0896639	intron-variant	RNF157	GRCh38.p7	17:76194743	AGAGCAGGCCGGGCA[C/T]GGTGGCTCACACCTG	114804
rs183744197	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76232750	TCTGCATTCTCAACA[C/T]TTGACACTGTCTGCC	114804
rs183810197	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157	GRCh38.p7	17:76156079	CCTCTTCCCTCTCAA[A/G]CCAGGGCCTACTTGT	114804
rs183858537	snp	C/G	0.00597247	0.0543191	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153531	GGCCTCAGAGCAGCA[C/G]GGGGAAGAGTCTGGC	114804
rs183861145	snp	A/C			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146138	TCCAATCCTCCACAG[A/C]CTCCTGTGGGCTCAC	114804
rs183874590	snp	A/C	0.0138799	0.0821421	intron-variant	RNF157	GRCh38.p7	17:76174084	TTAATAATAAAAAAA[A/C]AAACCGCTGAAGTTC	114804
rs183881953	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76186705	AGCACTTTGGGAGGC[C/T]GAGGCGGGCAGATAA	114804
rs183928026	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76230860	AAAAAAAAAAAAAAA[A/G]AGAGAGAGAGAGAGA	114804
rs184163680	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76224447	TCCTAGTAAATTTTC[A/G]TATATTTGAAAAAAT	114804
rs184225574	snp	C/T	0.00914312	0.0669923	intron-variant	RNF157	GRCh38.p7	17:76157080	CAAGCGATTCTCCTG[C/T]CTCAGCCTCCCGAGT	114804
rs184253399	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76143182	AACCTAGGTATGCCT[C/T]GGACATGGGACTGAG	114804
rs184270487	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76161375	CAATTTTCCACAGTA[A/G]TAAGTTGGTTTTAAC	114804
rs184275064	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76227601	AAGAGGTAGTGGCCC[A/G]GCATGGTGGCTCACG	114804
rs184276415	snp	A/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76183986	GTTGAGGCCAGGAGT[A/T]TGAGACCAGCCTGGC	114804
rs184279328	snp	A/C	0.0217236	0.101931	intron-variant	RNF157	GRCh38.p7	17:76200255	TTGTCAAAAAAAAAA[A/C]CAAAAACAAAAACCA	114804
rs184286448	snp	G/T	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76219457	AAGATATATACATAT[G/T]AATTAATATTTTTAA	114804
rs184310019	snp	A/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154156	TAAGAAGACGATCTT[A/T]CCTCTAACAGCCCCA	114804
rs184320737	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76174335	GCAGAGCTCTTTAAC[A/G]TGTGAGCCAAGAGTT	114804
rs184325771	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76191781	CCTGTCTAAAAAAAT[A/G]TTAAAATGTAAAGAT	114804
rs184331175	snp	A/G	0.0314385	0.121371	intron-variant	RNF157	GRCh38.p7	17:76210407	CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC	114804
rs184338601	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76228718	ACCTGAGGTCAGGAG[A/T]TCGAGACCAGCCTGG	114804
rs184349885	snp	C/G/T			intron-variant	RNF157	GRCh38.p7	17:76210368	GGAGGCCAAGGTGGG[C/G/T]GGATCACGAGGTCAG	114804
rs184395180	snp	G/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147544	CCAGGGCAGAACATC[G/T]GTTACTTGTGGAAGA	114804
rs184398773	snp	C/T	0.0126979	0.078662	intron-variant	RNF157	GRCh38.p7	17:76167884	GCAATATATTGTGGG[C/T]TTCTCTGAATGATCA	114804
rs184403300	snp	A/G	0.00438332	0.0466095	intron-variant	RNF157	GRCh38.p7	17:76187686	GCAACCTCCACATCC[A/G]GGGTTCAAGCGACTC	114804
rs184405647	snp	C/T			utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142650	CCAAAGCAAAGTGAG[C/T]GACCAGCGTGCTAAA	114804
rs184414872	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76203640	GTATTTTTGTAGAGA[C/T]GGGGTTTCACCACGC	114804
rs184420105	snp	A/G	0.0142736	0.0832652	intron-variant	RNF157	GRCh38.p7	17:76223186	TGAGCCACCGCACCC[A/G]GCCTTTTTTTTTTTT	114804
rs184486419	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76227923	GGTCCCCAAATCTAG[C/T]TATATTTATTCCAGA	114804
rs184534702	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76159907	TGTCTCTTCTTCCCA[A/T]TTTTTTTCTGTGTAC	114804
rs184573282	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76191255	CTGAGGCAGGAGGAT[C/T]GCTGGAGCCCAGGAG	114804
rs184589081	snp	C/T	0.00795532	0.062565	intron-variant	RNF157	GRCh38.p7	17:76160550	AATGTGGTTGAACTT[C/T]TTAAAAAATTCTATG	114804
rs184727003	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76183023	CAACCTCCGCCTCCC[A/G]GGTTCAAGCGATTCT	114804
rs184746428	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76156884	GGATGCAAAGTTCTA[C/T]GAACTGTATCTCCAT	114804
rs184748824	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76178986	AAAGATCTGAAGACA[C/T]AAATTTATTTATTTT	114804
rs184762696	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76194978	CGAGATAGCACCACT[A/G]CACTCCAGCCTGGGT	114804
rs184857490	snp	G/T	0.0387552	0.1337	intron-variant	RNF157	GRCh38.p7	17:76223348	ATGTGCCACCAAACC[G/T]GGCTAATTTTTGTAT	114804
rs184898229	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76235736	ATCTATGGCTGGGTA[C/T]GGTAGATCACTTCTG	114804
rs184901134	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76237361	TAGCCGCTTTCCAGC[A/G]AGCCAGATAGTGGTC	114804
rs184934564	snp	A/G	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76199101	GAGGGAATAATGAAG[A/G]AGTGAGCCAGTTAGT	114804
rs184946457	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76197322	TTAAGAGGACTGTTT[C/G]ATTGAAAAGAGAAAA	114804
rs184954559	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76215591	CCTGTGGAGAAGCCA[C/T]AGGAAGGAAGACAGA	114804
rs185048079	snp	A/C/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76218736	GTCAGGAGTTTGAGA[A/C/G]CAGCCTGTCCACCAT	114804
rs185080841	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76190734	ACCACGATGAAACCC[C/T]GTCTCTACTAAAAAC	114804
rs185094226	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76155022	CTCTTGAACTCACTC[C/T]ACACCAGTGACCCTG	114804
rs185095983	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76200857	CAACTGTTTCTAAAG[A/G]TGAATTACTGCATGT	114804
rs185096269	snp	A/C	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76175232	AGCATACTTTAATCA[A/C]TTCCATATTATTCAA	114804
rs185102652	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76219744	GAAACTATTCCCAAG[A/G]ACTTTAAGAGACTGT	114804
rs185112777	snp	C/T	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76193552	CCCACCACCCCCCAC[C/T]CACGGACACATACAA	114804
rs185129635	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76237770	CCAGCCTGGGCAACA[C/T]AGTGAGAGAGTGTCT	114804
rs185142118	snp	C/G	0.00517822	0.0506191	intron-variant	RNF157	GRCh38.p7	17:76238056	ACCACTTCATTCCAG[C/G]CTGGGCGTGACAGAG	114804
rs185169136	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152952	GGTCCATAATTTTGC[A/C]TATCAAATCAGAATG	114804
rs185184160	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76214633	ATGCTATGAAAGAAG[A/G]CTACACACATACCCT	114804
rs185184860	snp	C/G	0.0154538	0.0865337	intron-variant	RNF157	GRCh38.p7	17:76173254	TTGCGCCACTGCACT[C/G]CAGCCTGGGTGACAG	114804
rs185206284	snp	C/T	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76209720	AAACAGATGCAAACA[C/T]CAAGTCCATGTTATT	114804
rs185237075	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76148912	ACCCCAGGGCCTTCA[C/T]AGAACTATCACTTGC	114804
rs185241916	snp	C/G	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76170105	CTTAGGTTTTCCTAT[C/G]CAGGCAGGTCCAATT	114804
rs185267532	snp	A/G	0.00557542	0.0525036	intron-variant	RNF157	GRCh38.p7	17:76179591	CCAGCTACTAGGGAG[A/G]CTGAGGCAGAAGAAT	114804
rs185290355	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76195931	ATTGCCACGGCAACA[C/T]CTGGAAGTTACCACC	114804
rs185361992	snp	C/T	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76234188	TTTTCAAGGTTCATC[C/T]AGGTTGTAGCACATA	114804
rs185407439	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76181526	CAGCCACAATGGATA[C/T]GTCAGTCAGCGTTTA	114804
rs185527269	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76148416	GGACTACAGGCACTC[A/G]CCACCACGCCTGGCT	114804
rs185690963	snp	C/T	0.00597247	0.0543191	intron-variant	RNF157	GRCh38.p7	17:76232276	GCCTGTAGTCCCAGC[C/T]ACTTGGGAGGCTGAG	114804
rs185707539	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76168739	TTGGGTTATTCTTTC[A/G/T]TATCGGTGGAGCACG	114804
rs185720538	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76204610	AGTGCAAAACTCTAT[A/G]TTACAAATGGATATA	114804
rs185840219	snp	C/T	0.00755907	0.0610114	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213227	TGTGATATTGTAAAA[C/T]ATATGTTTGATCTTC	114804
rs185842813	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76187862	CTTAGCCTTCCAAAA[C/T]GCTGAGATTACAAGT	114804
rs185860408	snp	A/G	0.00636936	0.0560724	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144576	CCTCCCAAAGTGCTG[A/G]GATTACAGGCGTGAG	114804
rs185902880	snp	A/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76158140	AGATAGCAAGAATAT[A/T]AATGCTACAAGGGCA	114804
rs185904423	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76239775	GCAGGTAGGCTTTGG[A/G]CCGGGCCGGCCGGGT	114804
rs185936399	snp	C/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76180911	ACAACATGCCTGCCC[C/G]TCTCACCAGCCTGTA	114804
rs185957528	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76164034	CATCTACAGGAAGGC[C/T]TTTCTTTGCATCTCG	114804
rs185959949	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76186171	CAAGCTGAAAAACTC[C/T]AAGCTGTCCTTTCAT	114804
rs185966125	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76184552	CCTATTTACCCAGAT[G/T]CATCCCTGAGACAGA	114804
rs185974055	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76202163	ACACACACACACACA[C/T]ACACACACGTGCATG	114804
rs185980316	snp	G/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76221083	CCGTGTTTGCACCAC[G/T]GCACTCCAGCCTGGG	114804
rs186031389	snp	C/G	0.0111196	0.0737302	intron-variant	RNF157	GRCh38.p7	17:76205322	TTTTTTTTGTAGAGT[C/G]GGGGTTTTGCTATGT	114804
rs186038926	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145882	CTGGAGGGAGGACAG[C/T]GTGAGGCTCCAGTCC	114804
rs186050253	snp	C/G	0.00478085	0.0486577	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144520	CGCCGTGTTAGCCAG[C/G]ATGGTCTCGATCTCC	114804
rs186097645	snp	A/C	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149849	GACCACCCTGACCAA[A/C]ATGGTAAAACTCCGT	114804
rs186099755	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76171210	TTTTTTATTTTTTAG[C/T]TGGAGTCTCACTCTG	114804
rs186115929	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76189061	AAGAACAAGGAAAAA[C/T]TGAGAAACTAGCACA	114804
rs186128561	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76225370	GTCCTTTGCCAAAAA[A/G]ATTAGTATATATAAG	114804
rs186178961	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76162074	TTACTGACAAGGCAG[C/T]GTGGCTGAAGAGCTA	114804
rs186307889	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76216267	GGCAGTAAAAATCCA[C/T]GGATGATTGGCTTAG	114804
rs186440872	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76196609	AAAGCAAGGGCCGAA[A/G]TATGTACGGGAGTGT	114804
rs186448666	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76235868	TTAAACATTAGCCAG[C/G]CATGGTGGTATGTGC	114804
rs186449421	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76214966	ATTTCTATTATCTAA[C/T]TCTCCCATGAAGGTA	114804
rs186519951	snp	C/T	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76162782	AGATGCTTTTATTTA[C/T]TTATGTTTTCTCTTT	114804
rs186531243	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76201642	TTGTGTAGCTATAAA[C/T]ATATGTACATAATGC	114804
rs186531421	snp	A/G	0.00159617	0.0282053	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151475	TGTGGCTGTTCTGAA[A/G]CTGAAGTGAGTCTTC	114804
rs186552738	snp	C/G	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76172478	TGCCTGTAATCACAG[C/G]TACTTAGGAGGATAA	114804
rs186573024	snp	C/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76229236	TATCTTAAGGGTTCA[C/G]CCCTCTCCTCTTCCT	114804
rs186590417	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76192565	ATATGCCCATGGTGA[C/T]TCTTTAGATTTTGAA	114804
rs186609844	snp	C/T	0.00478085	0.0486577	intron-variant	RNF157	GRCh38.p7	17:76217899	ATCTCCAAGATTATA[C/T]GTAAACCGTAAGGTA	114804
rs186666182	snp	A/G	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76220362	AAGGAATAAGTCTAA[A/G]TCAATGAGTTCGTAA	114804
rs186672110	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76237029	AAGGCTTTCACTGTA[C/T]ACGTTTTCATTCTTT	114804
rs186685013	snp	A/C			intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76154702	TCCCAAACCCCATCC[A/C]GATCCTCCATTGACA	114804
rs186834607	snp	A/C	0.00835141	0.0640778	intron-variant	RNF157	GRCh38.p7	17:76210844	GAGTCTCATTCTATC[A/C]CCTAGGCTGGAGCGC	114804
rs186905835	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76174846	TGACTCTTACATTCA[A/G]TAGAAATTATCTTCA	114804
rs186965558	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76172847	GGTGGCGGGCAGTGG[A/G]AATGTATCAGACTAA	114804
rs186967579	snp	A/G	0.0221141	0.102801	intron-variant	RNF157	GRCh38.p7	17:76190187	TTTTTTTTTTTTTTT[A/G]AAATAGATTCTCACT	114804
rs186975616	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76208871	CCCAGCTAGTCAGGA[A/G]GCTGAGGCAGGAGAA	114804
rs186988816	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76227307	TGTATTTTTAGTAGA[A/G]ACAGGGTTTTACCAT	114804
rs187011765	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76197638	GCAGTGGTGTGAACA[C/T]AGTTCACTGCAGCCT	114804
rs187105386	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76176085	AAAGTTTGTGCCTTG[A/C]TGGCCTTGCATTCAT	114804
rs187108057	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146993	CCTCAGGCTCTAGTA[A/G]CAGTCTCTGGTGCTT	114804
rs187110450	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76194285	TATCTCTATCGTTTT[G/T]CTCTTTCCAGAATGA	114804
rs187112127	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76167368	GGACCTGAAGGACTA[C/T]ACCACCATTTGTCAC	114804
rs187118128	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76211596	TAGAACAGTGCTTAG[A/T]ACATAGTGTGCACTT	114804
rs187171269	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76230163	AATGATCATAATGTG[A/T]GTCCTTTGGCAATCC	114804
rs187318715	snp	A/T	0.0115144	0.0749975	intron-variant	RNF157	GRCh38.p7	17:76207440	GGGGAAAAAAAAAAA[A/T]TGGCTTTGATGGATT	114804
rs187411138	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76171980	CAAGTGGACAGAGTA[A/G]CTGGCAATGGCAGGC	114804
rs187422282	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76235110	GGTAGCGATAGTCCT[C/T]CAACTTTGTTCCTTT	114804
rs187433526	snp	A/T	0	0	intron-variant	RNF157	GRCh38.p7	17:76198525	GGGGCCTGAACATAC[A/T]CTAATTACCACACCC	114804
rs187515891	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76226746	CCAAACCCGACTGGT[C/T]GAAGGGGGACATCAA	114804
rs187591742	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76226071	CACCTGGAGATGGGA[A/G]GCTCCTATTTGGAGA	114804
rs187617461	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146334	TGAGAGAATGCGAGC[A/G]TTGGTGAGTATCTGA	114804
rs187632479	snp	A/G	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76186900	AGCTGAGATCGCACC[A/G]CTGTACTCCAGCCTG	114804
rs187665707	snp	C/T	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150019	GGCTGGGCGACAGAG[C/T]GAGACTCTGTCTCAA	114804
rs187674937	snp	G/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76189399	GATCTATGAGCAGAA[G/T]GCGTGGGTCTCAGCT	114804
rs187754959	snp	C/G			utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142897	CAGGAAGGAGCCCTG[C/G]GTCTCCATAGTTAGG	114804
rs187760504	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76208295	ACTCACAAACAGGAT[A/G]TGGGCAGAGTTTCTG	114804
rs187823687	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241041	GGGAGAGGGGTCCCA[C/T]GGTGCATTCGCATGT	114804
rs187846540	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76156924	CCTTCCCTCCAGGCG[C/T]TCCTCTTTTGTCTTA	114804
rs187854312	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76179273	GTGGCACACACCTGT[A/G]GTCCCAGCTACTCAG	114804
rs187858802	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76221600	TGTATACAATCAACA[A/G]AAACCAGGACTTTCT	114804
rs187864579	snp	G/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76195013	GAGCGAGACTCTGTC[G/T]CAAAAAAACAAAACA	114804
rs187876714	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213282	CTTAAAATCCTTGGA[A/C]TATCCAGGCCGGCAT	114804
rs187908189	snp	A/G	8.63506e-05	0.00657022	intron-variant	RNF157	GRCh38.p7	17:76164829	AGTTATGACAAGGAA[A/G]GGAGGGTAATAAAGC	114804
rs187993129	snp	A/G	1.65211e-05	0.00287407	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159342	CTACTCACTTGGAGA[A/G]ACTCTTTTTGAGTTT	114804
rs188008977	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76182094	GCATCTGGTGCCCTG[C/T]ATGCTTGGATACAAC	114804
rs188014851	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76198402	TAATTGATTCCAAAA[C/T]TGCCACAGAGATCTT	114804
rs188022695	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76216885	AAAAGAGCAAGACCC[C/T]GTGTCAAAAAAAAAC	114804
rs188049798	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76236532	TACATCCAAATACAG[G/T]AGAACCGTGCTCTAA	114804
rs188080857	snp	A/C			intron-variant, upstream-variant-2KB	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76141953	AGGCTTCTGCAGAAG[A/C]GCACTCACTCCTCTG	114804
rs188095055	snp	G/T	0.00159617	0.0282053	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153703	CTGAATTATGGTAAA[G/T]GAAGATTATTACAAC	114804
rs188097049	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76174199	AGCCCTTTCCTTCGG[G/T]GAGGCCATGCGGTAT	114804
rs188105354	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76191340	AATTAGGGCTGGGCG[A/C/T]GGTGGCTCACACCTG	114804
rs188116579	snp	A/C/T			intron-variant	RNF157	GRCh38.p7	17:76203151	ATGCACCACCATGCC[A/C/T]GGCTAATTTTTGTAT	114804
rs188116966	snp	C/T	0.00517822	0.0506191	intron-variant	RNF157	GRCh38.p7	17:76210380	GGGCGGATCACGAGG[C/T]CAGATCGAGACCATC	114804
rs188246806	snp	A/G	1.65209e-05	0.00287405	missense, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156281	ATAGCTCCAGATGAC[A/G]ACAAGGTGAGATTCT	114804
rs188267913	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76232007	ACGATATATAGTCTT[C/G]CATCTAGTTTCTTTC	114804
rs188289566	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76238141	GGTCATGGCCAAACT[C/T]TGTCAACGGTTCCTT	114804
rs188392729	snp	C/G	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76187478	CATGAGCCACGGCGT[C/G]TGGCCAGGATTTTAT	114804
rs188406937	snp	C/T	0.00795532	0.062565	intron-variant	RNF157	GRCh38.p7	17:76222969	GATCCTGGCTCACTG[C/T]AAGCTCCGCCTCCTG	114804
rs188408299	snp	C/T	0.00993419	0.0697739	intron-variant	RNF157	GRCh38.p7	17:76181673	AGCACTTTGGGAAGC[C/T]GAGACAGGCAGATCA	114804
rs188414775	snp	A/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151806	TAACTCGACCTCTCC[A/G]TTGGGATCCAAATCC	114804
rs188463051	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157	GRCh38.p7	17:76155854	AAGTGGCCGTATCTT[A/G]CCCTCCCCTAAAAGT	114804
rs188496463	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76143027	GTTGGCCACTGACCT[A/G]TCCTCATCAGGCTGA	114804
rs188510617	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76160778	TGGTTCTTGCTTTCA[A/G]GCTTAGAGAATCCTT	114804
rs188547055	snp	A/C	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76176901	CAGCCACTGTGCCCA[A/C]CCTGCCGAGGGTGCC	114804
rs188584924	snp	A/G	0.212728	0.247206	intron-variant	RNF157	GRCh38.p7	17:76210511	AGGAGAATGGCGTGA[A/G]CCCGGGAGGCAGAGC	114804
rs188594833	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76228778	AATACAAACTTAGCC[A/G]GGCGTGGTGGTGGGC	114804
rs188690321	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76158720	GCCTCCTGAGTAGCC[A/G]AGTAGGTCTGGGCTA	114804
rs188707058	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76233931	GTATATTGACCGTGT[C/T]ATACAACTATTCACC	114804
rs188727424	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76195547	GTATGCATACATATA[C/T]ACAACAAAATACATG	114804
rs188735445	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76170482	CATTAGCTGTGCCTG[A/G]GTCTCTCTTGTCCAG	114804
rs188735597	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76214377	TCCTATATCCGCAGA[C/T]GCACACATTTCTTTG	114804
rs188739412	snp	C/T	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76188580	GCAAAGATGGTGCAA[C/T]AGATGCAACAGATAA	114804
rs188755587	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76203981	ACTGTGTTAGCCAGG[A/G]TGGTCTCGATCTCCT	114804
rs188767418	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76223262	GTCCAATCTCTGCTC[A/G]CTGCAACATCCGCCT	114804
rs188818306	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149464	GGCGCCAAGACGGCC[A/G]GTGGTATCTCAGCCC	114804
rs188833212	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147716	TCAGCCTCATTCTCA[C/T]AGTAAGCCTGTCTGC	114804
rs188837348	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76167917	AGCATAGGTCTACCT[C/T]TTCATTCTGAATGAT	114804
rs188902667	snp	A/G	0.0217236	0.101931	intron-variant	RNF157	GRCh38.p7	17:76173261	ACTGCACTCCAGCCT[A/G]GGTGACAGAGCGAGA	114804
rs188966112	snp	A/G	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76232332	GGTCGACGCTGCAGG[A/G]AGCTATGATCGCACC	114804
rs189004164	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76162161	CAGTGCGTCCACACA[C/T]TTAGCTTCACTTCTT	114804
rs189009416	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76202589	CACCTCATGTGTGGA[C/T]CACATCATTCAGCAA	114804
rs189010790	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76228047	GTTGCTTCCTGTTTT[C/T]TACAAATGGAATTCA	114804
rs189110625	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76227665	GGCGGATCACCTGAG[A/G]TCGAGAGTTGGAGAC	114804
rs189195006	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76190826	GACAGAAGAATGGCA[C/T]GAACCCGGGAGGCGG	114804
rs189247073	snp	C/T	0.00597247	0.0543191	intron-variant	RNF157	GRCh38.p7	17:76215010	AAAGGACACATCCCA[C/T]AATATACCTTTATCA	114804
rs189295759	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76185473	TCAGAGATTAGTCCT[C/T]TCTTTTTTTTTTTTG	114804
rs189296918	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76235349	ACTACAGGCTTCTGT[C/T]ACCATGCCTGGCTAA	114804
rs189342143	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76237807	AAAACTTGCCTGGGC[A/G]TGGTAGCTCACACCC	114804
rs189374204	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76184434	CCTGAGATACATAAC[A/G]TGTCCAAGGCTTACC	114804
rs189386569	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76200493	TTCTATGATTCAACT[C/T]GTATGAGGTACCTAG	114804
rs189394949	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76219509	TCATAATAATCTTAA[A/G]GTGATTATCTATAGG	114804
rs189452055	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144293	AGGGAAATCATCTTA[A/G]CTGGGGGATTCTCAG	114804
rs189467738	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76161471	ACGTAGAGAAGCATG[A/G]AAAGTTTAAAAAAGC	114804
rs189541527	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76183380	AGGTTAGAGACCCCA[A/C]TGAAAGAAAAAATGC	114804
rs189546525	snp	A/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154551	CGAGCCACATTACCC[A/T]TATATGCTCAGAATG	114804
rs189559133	snp	A/C	0.00252144	0.035417	intron-variant, missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155272	CATCCTGCTCTCCAG[A/C]TGGGAGGCCAGCAAA	114804
rs189563171	snp	A/C	0.00835141	0.0640778	intron-variant	RNF157	GRCh38.p7	17:76219304	CATAAAGACTATATA[A/C]ATTTTTACATATATT	114804
rs189563540	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76175300	ATGTTGTGGTGAATA[C/T]CCTTGTCCCTATATT	114804
rs189606441	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76220238	ACCAGATAACAAGGA[C/T]GCTCTCTAAACCTAC	114804
rs189658964	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76205632	TGGGAGGCTGAAGCA[A/G]AAGAATTGCTTGAAC	114804
rs189732305	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76179367	TCACTGCACTCCAGC[C/T]TGGGGGAGAGAGTGA	114804
rs189810496	snp	C/T	0.00557542	0.0525036	intron-variant	RNF157	GRCh38.p7	17:76157245	TGCCGGGATTCCAGG[C/T]GTGAGCCTCCGCGCC	114804
rs189820626	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76196049	AAAAGTGGGTATAAA[C/T]ATGATTACAAACCTG	114804
rs189827249	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76199359	CCTCACAGGCTCAAG[A/T]GATCCTTCCACCTCA	114804
rs189837787	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76174382	AGGTTTATGGTTGTC[C/T]TCATCATTTACCATC	114804
rs189843041	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76234481	CCCATTTTACATTCA[C/T]ACCGGCAGGGTATGA	114804
rs189844009	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76237436	TGACTCTGCCACTTG[C/T]TTTGTTCCACTGTTA	114804
rs189870253	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76193850	CAGATCTGAGATTAG[C/T]GCCTGGCCGAGGGCT	114804
rs189877985	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76211271	TCTTAGGCCTGTGCC[A/G]TGCTCTACTCCTGGA	114804
rs189928618	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76224484	CTACATGACATTTCA[A/G]TAACAATAAGCTTTA	114804
rs189954132	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76230261	CTAATTTCCCCGGAT[C/T]TTGAGGCAAAGTAAA	114804
rs189979486	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76157167	GAGACGGGGTTTCAC[C/T]ATGTTAGCCAGGATG	114804
rs190052161	snp	C/T	0.00318978	0.0398085	intron-variant	RNF157	GRCh38.p7	17:76211770	ACCTGGCGGCTATTA[C/T]TACAAAGCCTCCTGC	114804
rs190063437	snp	C/G	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76179594	GCTACTAGGGAGGCT[C/G]AGGCAGAAGAATTGT	114804
rs190084324	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76214782	AATAACCAAATGAAA[C/T]CAGCAGTCAGGGGCC	114804
rs190109425	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76189761	GAGAAGGGACCCTCC[A/G]AAGCTGGGACTCAGA	114804
rs190117907	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76208392	CCAATCCTGATCCCT[C/T]ACAGGCTGTGCAGTC	114804
rs190128081	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76226812	TTTCGGTCATGTTGC[A/G]GTGCTTTGCTGGAAT	114804
rs190147241	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76163130	AATGGTGTGTACCCC[A/G]CACCATGAAGCCACC	114804
rs190164071	snp	A/G	0.0130921	0.0798413	intron-variant	RNF157	GRCh38.p7	17:76185691	AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT	114804
rs190194565	snp	A/G	0.00438332	0.0466095	intron-variant	RNF157	GRCh38.p7	17:76235737	TCTATGGCTGGGTAC[A/G]GTAGATCACTTCTGT	114804
rs190235226	snp	C/T	7.61847e-05	0.00617143	missense, intron-variant, utr-variant-3-prime, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145320	CGGCGCTGGGCATTC[C/T]GACTGACGGCATTGT	114804
rs190289644	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76223386	AGAGACGGGGTTTCA[C/G]CATGTTGGCCAGACT	114804
rs190361207	snp	C/T	0.00318978	0.0398085	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76148563	GGAGCCACCGTGCCC[C/T]GCCTTTTTTTTTTTT	114804
rs190368993	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76188230	TCCAAGGTGACTTAC[A/G]TTCTCTTGTACTGCA	114804
rs190473893	snp	C/T	0.00398564	0.0444627	intron-variant	RNF157	GRCh38.p7	17:76171695	TTACCTTAATTTTGA[C/T]AACCACCATGAAAGG	114804
rs190489662	snp	C/G	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76189209	TAGTAATGTAACTGT[C/G]TTAATTTTCAGTCTG	114804
rs190617148	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76168915	CTGCCTTATTTTTCA[C/T]CTCCCAGCGTTGCTC	114804
rs190633038	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76204872	TCACTGAAACCTGTG[C/T]ATCCTGGGTTCAAGC	114804
rs190757469	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153372	AGCTCCTTGGCCAGG[C/T]GGGAGCCGTCAGGTC	114804
rs190788948	snp	A/G	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76207138	ATTTGGCTTTGGGCC[A/G]GGCTTGGTGGCTCAC	114804
rs190789082	snp	G/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76158979	CTAGCTGGATTTAGA[G/T]GTTTAAGAGATACGG	114804
rs190798018	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76225813	AATCTTTCAGGTACT[A/G]GATCTCCTTGGCCAG	114804
rs190799335	snp	A/G	0.0115144	0.0749975	intron-variant	RNF157	GRCh38.p7	17:76180477	TGGCAAATCATGAAA[A/G]AAGAGAATGTAAGGA	114804
rs190805049	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76196977	CCATCTGTCTTCCTC[A/C]TCTCTAGAGAGCATT	114804
rs190859001	snp	G/T	0.0189856	0.0955633	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144525	TGTTAGCCAGGATGG[G/T]CTCGATCTCCTGATC	114804
rs190879275	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241373	TTGGGCCGGCGGAAG[A/G]CGTCATTCCATTGCT	114804
rs190879740	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76157660	ACTGAGCAACAACAA[C/T]GTGCCAGGCACATGC	114804
rs191037094	snp	A/C	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76202188	TGCATGAGAAAGACA[A/C]CCGTTCCCACCATGG	114804
rs191047266	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76221253	ACCAAACCTCTCCCC[A/C]ACAAAAAAGACAACC	114804
rs191102088	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157	GRCh38.p7	17:76155923	ATATTTTAGAGCTCA[A/G]AACTCAGCCTTGGGG	114804
rs191111968	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76220453	ATTATTTTGGAAACT[A/G]GCAATTAAAGGGAAA	114804
rs191114443	snp	C/T	0.0170251	0.090679	intron-variant	RNF157	GRCh38.p7	17:76239822	CCTCGCCTACGACGC[C/T]GCAGCCCCGCTCCCC	114804
rs191116135	snp	C/T	0.00755907	0.0610114	intron-variant	RNF157	GRCh38.p7	17:76164465	TTCATTTCTCAAGTC[C/T]TTTGCTCAGATAAAG	114804
rs191120752	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76194382	CGCACTCAGCCACCA[C/T]AGGAGACTTTCAAAT	114804
rs191128178	snp	C/G	0.040671	0.13668	intron-variant	RNF157	GRCh38.p7	17:76186660	TCTCAGGTCTGGGCC[C/G]GGGGGGCAGTGGCTC	114804
rs191284146	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76215653	ATTCATTTTTAAAAC[C/T]TTCTACACAAGGAGC	114804
rs191348681	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76201664	ACATAATGCACACAC[A/G]TACATATATTATTTT	114804
rs191382334	snp	A/C	0.0138799	0.0821421	intron-variant	RNF157	GRCh38.p7	17:76239541	TTCCACCACCACCAC[A/C]CCCCCCACCCCCCGG	114804
rs191492206	snp	C/T	3.3083e-05	0.00406699	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76158497	AAGAGTTTTGGGAAG[C/T]GGATCTGTAGGAGTC	114804
rs191510547	snp	A/C	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76197358	TTCAGGTATAGCAAT[A/C]AAAAATGTAAAGCCA	114804
rs191526717	snp	C/G	0.0126979	0.078662	intron-variant	RNF157	GRCh38.p7	17:76187640	ACTCTGTCGCCCAGG[C/G]TGGAGTGCAGTGTGG	114804
rs191533990	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76214029	TCTAGTTCTGTGAGT[C/T]CCTCTAGCAAGTTAA	114804
rs191538677	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76203349	TAGATGGGGAAATTG[A/G]GACTCACTGATTGGC	114804
rs191595648	snp	C/T	0.00993419	0.0697739	intron-variant	RNF157	GRCh38.p7	17:76157059	GCAACCCCTGCCTCC[C/T]GGGTTCAAGCGATTC	114804
rs191604166	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76232619	CAGATTCATAGGAGT[A/G]GAACTGCTGAATCAT	114804
rs191608780	snp	C/T	0.0126979	0.078662	intron-variant	RNF157	GRCh38.p7	17:76179297	TACTCAGAAGGCTGA[C/T]GCAAGAGGATCACTT	114804
rs191611587	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147082	GAATTTGGGATCTTT[A/G]CTCCCTGGGGGTGGG	114804
rs191614740	snp	A/G	0.00438332	0.0466095	intron-variant	RNF157	GRCh38.p7	17:76195133	GAACAGAAAGGGCCG[A/G]AATCCCAAATGGCAG	114804
rs191619297	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76234054	CAGGCACAGCCACTG[C/T]GCCACTGCCACTAAT	114804
rs191657318	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149902	AGCCGGGCGTGGTGG[C/T]GGGCGCCTGTAATCC	114804
rs191702090	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76236074	TAAAGGAGATTATCC[C/T]TGATTATGTGGGTGG	114804
rs191757018	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76198121	TGAGTATTACTCAAC[C/T]GGGGCCTGCTGGACC	114804
rs191778266	snp	A/G	0.00318978	0.0398085	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151607	GTGGATTTTAGAAAA[A/G]CAGTTTTTGGAGCCC	114804
rs191780949	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76172576	CGTGCCATTGCACTC[C/T]AGCCTGGGCAACAAG	114804
rs191891681	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150077	CTCAAATCCTTTCCA[C/T]TGTCCTTGCCACAGA	114804
rs191905983	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76189504	TGAGCTCCATAACAG[C/T]GACCTCAAAAGTTGT	114804
rs191918826	snp	C/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76226089	TCCTATTTGGAGAGC[C/G]CCTGGTAGAGGGGCT	114804
rs192030679	snp	A/G	0.0023933	0.0345097	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145961	GTTTGCTACTAGCTG[A/G]TGCCATCAGCCCAGC	114804
rs192033134	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76210893	CACTGCAACCTCCAC[C/T]TCCCGGGTTCAAGCG	114804
rs192042510	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76223271	CTGCTCGCTGCAACA[C/T]CCGCCTCCCAGGTTC	114804
rs192042949	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76181769	AAAAATCAGCTGGGT[A/G]TGGTGGCGTGTGCCT	114804
rs192064343	snp	C/T	0.00597247	0.0543191	intron-variant	RNF157	GRCh38.p7	17:76216361	GCAGGCAACAGGGTT[C/T]GATTAGAAATGCCCT	114804
rs192201405	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76172169	GGGACAAATAAAATA[C/T]AAAAAATTAAGAGAG	114804
rs192204610	snp	A/C	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76227424	CTGCGCCTGGCCTAT[A/C]ATCTCTTCAGAGGAC	114804
rs192206479	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76183478	TTGTTTTTTAGAGGT[A/G]GGGTCTTGCTATGTT	114804
rs192214223	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76199849	TATTAAGGATGAAAA[A/G]TAATATAAGTTGAAT	114804
rs192222409	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76207454	ATTGGCTTTGATGGA[C/T]TATCCTAAGTGGTAG	114804
rs192284904	snp	A/G	0.00953873	0.0683987	intron-variant	RNF157	GRCh38.p7	17:76190354	ATATTTTTAGTAGAG[A/G]CGGAGTTTCGCCATG	114804
rs192286785	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76161084	CTTTGAGGTTTCACC[C/T]TAATATCAGCACTTA	114804
rs192294432	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76209535	CTGCTAGTGTATTCC[A/G]TGTGTGGCCCAATGT	114804
rs192297891	snp	C/T	0.00478085	0.0486577	intron-variant	RNF157	GRCh38.p7	17:76229512	GCTTCTCCCTTCCCA[C/T]ACTCAACTCCCAAAC	114804
rs192355766	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76154898	GGTCTGTATAGGTCT[A/G]TATGTGCCCTAGCAC	114804
rs192378973	snp	A/T	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76236926	AGAAACTCTAAAAGA[A/T]TTCCAAAGAAACCAA	114804
rs192379256	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76193043	AGGCTGGTCTCAAAC[G/T]CCAGAGCTCAAGTGA	114804
rs192397602	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76198493	GGGAAAATCCACTAG[C/T]TGGCTGCGTCCTTTG	114804
rs192402061	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76216912	AAACAAAAACAAAAA[C/T]AAAAAACAAACAAAC	114804
rs192456618	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, downstream-variant-500B	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142098	TTAAGAGTAGAGGGA[C/T]TCTGGGGACTGTGTC	114804
rs192471726	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76182379	GAAAGATGAAATTGC[C/T]AGACCATGCCCAAAT	114804
rs192489416	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76165441	AGCAAACGGGTTACA[C/T]GTGTCTCACACGAAA	114804
rs192508096	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76202787	GGGCCTTCTCTGCAA[A/G]GTTATAAATTGGTCC	114804
rs192523830	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76156709	GAGGACTTCCTGCCT[G/T]CAGGGTATCTCCACG	114804
rs192535224	snp	C/T	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76187815	GTTGGTCAGGCTGCT[C/T]TTGAACTCCTGACCT	114804
rs192540547	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76204058	AGGCGTGAGCCACCG[C/T]GCCCAGCCCATAAAA	114804
rs192589660	snp	A/G	0.0685596	0.171987	intron-variant	RNF157	GRCh38.p7	17:76223016	CTGCCTCAGCCTTCC[A/G]AGTAGCTGGGACTAC	114804
rs192712006	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142904	GAGCCCTGGGTCTCC[A/G]TAGTTAGGCTGTGCC	114804
rs192724375	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76183022	GCAACCTCCGCCTCC[C/T]GGGTTCAAGCGATTC	114804
rs192729163	snp	C/G	0.00597247	0.0543191	intron-variant	RNF157	GRCh38.p7	17:76218414	GGGAGGCCAAGGCAG[C/G]AGGATTGCTTGAGCC	114804
rs192790006	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146359	ATCTGACTCCTAGAA[C/T]AGCCTGTGCTCAGGC	114804
rs192800155	snp	A/C	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76186966	ATAAATAAATAAATA[A/C]ATAAATAAATAAATA	114804
rs192810273	snp	C/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76222323	CTGCACTCCAGCCTG[C/G]GTGACAGAGCAAGAC	114804
rs192916809	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76160147	TTTTCCTTTGTTTCT[C/G]AAGCCTCTTTATATA	114804
rs192927180	snp	A/C	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76198868	GCAAAGTCTCCTCCC[A/C]CCCTCTGGATGCCAC	114804
rs192939380	snp	C/G	0.00636936	0.0560724	intron-variant	RNF157	GRCh38.p7	17:76237306	AGGACAGATGATGGT[C/G]CTTCTTTCCGAAACA	114804
rs192989012	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76237723	AATGGGAGGCCAAGG[C/T]GGGAGGATTGCTTGA	114804
rs192992963	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76173089	CAGGAGATCGAGACC[A/G]TCCTGGCTAACATGG	114804
rs193033467	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76190833	GAATGGCACGAACCC[A/G]GGAGGCGGAGCTTGC	114804
rs193043592	snp	A/C	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76227871	AACAAGAGCGAAACT[A/C]CATCTCAAAAAAAAT	114804
rs193100305	snp	C/T	0.00557542	0.0525036	intron-variant	RNF157	GRCh38.p7	17:76177337	GCAGGCTCGGAAGTG[C/T]CTGCTCCTGCCGCCT	114804
rs193101347	snp	C/T	0.0240643	0.107019	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76148335	GCAGTGGCGTGACCT[C/T]GGCTCACTGCAAGCT	114804
rs193104907	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212928	TCTAATCCCAGAGTG[C/T]TTTCTTTTCCTGATT	114804
rs193183881	snp	C/T	0.00557542	0.0525036	intron-variant	RNF157	GRCh38.p7	17:76219386	AATCATATCAATAAA[C/T]ACAAATAGGCTTAAT	114804
rs193195033	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152885	GCTGGGTGTGTTTAG[C/G]ACCACATGGCTCTGC	114804
rs193222458	snp	A/C/G	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76210320	GAGAACCCGCCGGGC[A/C/G]CAGTGGCTCATGCCT	114804
rs193257678	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76194832	CATCCTGGCTAACAT[A/G]GTGAAACCCCGTCTC	114804
rs193258411	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76168579	AGGTCCCTTGGACTT[A/G]CTCCCATCTGTACTT	114804
rs193269448	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76232211	AACGTAGTGGGACCC[C/T]GTCTTTACAAAACAT	114804
rs199562423	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76210605	AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA	114804
rs199566306	snp	A/C/G	0.00159617	0.0282053	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147400	AGCACCACCACCACC[A/C/G]CCGCCGCCGCCACCA	114804
rs199575889	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76233336	TTCAGAAAGTGGCTT[A/C]TCTTTTCAACTTTTT	114804
rs199579320	snp	A/G	3.29815e-05	0.00406075	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76165532	CAGCAGTACATGGCA[A/G]TGGCCAAAATACTCT	114804
rs199656634	snp	A/G	0.000329804	0.0128372	intron-variant	RNF157	GRCh38.p7	17:76161514	TGCTTCAGAGGGGCC[A/G]TGGTTCCGAGCCCAA	114804
rs199728981	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76210386	ATCACGAGGTCAGAT[C/T]GAGACCATCCTGGCT	114804
rs199750475	in-del	-/A	0.0498117	0.149749	intron-variant	RNF157	GRCh38.p7	17:76201510	AACAAGCTTATTTCT[-/A]AAAAAAAAAATAAAG	114804
rs199797852	in-del	-/T	0.195214	0.243923	intron-variant	RNF157	GRCh38.p7	17:76190171	ACTGCTTGCTCTCTC[-/T]TTTTTTTTTTTTTTT	114804
rs199811091	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76227742	ATTAGCCGGGCGTGG[C/T]GATGCAGGCCTGTAG	114804
rs199850393	snp	A/C	0.000214371	0.0103508	intron-variant	RNF157	GRCh38.p7	17:76165581	TGAGTGAAGAAGCCC[A/C]AACAGCACATCTTGA	114804
rs199850445	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146137	ATCCAATCCTCCACA[C/G]CCTCCTGTGGGCTCA	114804
rs199974386	snp	A/G	9.4753e-05	0.00688241	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155689	GTGCTGATCTGGGAG[A/G]ATGCCATGGACATGA	114804
rs199976512	in-del	-/GGCCA			intron-variant	RNF157	GRCh38.p7	17:76220678	TTTTTTAGTTAGCTG[-/GGCCA]GGCGCAGTGGCTCAC	114804
rs199996462	snp	C/T	0.00013214	0.00812726	splice-acceptor-variant, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152467	GCACGTCCTCTGGCC[C/T]GTAACGGAGTTAATG	114804
rs200011009	snp	C/T	0.00399206	0.0444982	intron-variant	RNF157	GRCh38.p7	17:76226118	CTATGCTGAGGAGAC[C/T]CCAGATAGGACTCTG	114804
rs200020230	snp	C/T	3.30191e-05	0.00406306	intron-variant	RNF157	GRCh38.p7	17:76155237	GGGGGCACCACTCCG[C/T]GCTGTTGGGGTTACC	114804
rs200041665	snp	C/T	0.000164829	0.00907674	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76161949	GGTGTCCCGGACATC[C/T]GAGAGACACACCACA	114804
rs200093330	in-del	-/TCT	0.0225045	0.103662	intron-variant	RNF157	GRCh38.p7	17:76202907	TTACTTCCTAACTGG[-/TCT]TCTTATTTTCTGTCT	114804
rs200106408	in-del	-/TA			intron-variant	RNF157	GRCh38.p7	17:76220656	CTACAAATTTATTAT[-/TA]TTTTTTTTTTTTAGT	114804
rs200118442	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76217962	TAACAAGTACATAGT[C/T]TTAGTTTTATAAAAT	114804
rs200140803	in-del	-/AAT			intron-variant	RNF157	GRCh38.p7	17:76215555	TAAAAAAAAAAAAAA[-/AAT]GAGATTCAGTACTTT	114804
rs200164730	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76224389	CAATTAAACCCATTT[C/T]CTATTCTTCTACAAT	114804
rs200167921	snp	C/T	0.000198666	0.0099646	intron-variant	RNF157	GRCh38.p7	17:76167131	TGGGAATGTAGCTAT[C/T]GATACAAGTGGGAGG	114804
rs200198629	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76180823	AGTAACATTCACATT[C/T]GCATTATCGTGCGGC	114804
rs200215015	snp	C/T			utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144324	ATTCAAGGGCTCCTT[C/T]TTTTTTTTTTTTTTT	114804
rs200236039	in-del	-/A	0.00478085	0.0486577	intron-variant	RNF157	GRCh38.p7	17:76228101	TTTCTAAAAAGAAAT[-/A]AAAAAAAACCATTTA	114804
rs200237871	in-del	-/A	0.0248432	0.108648	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150629	AGCTAAGAAAGAGAC[-/A]TCATCTTCACCCAAC	114804
rs200240307	snp	C/T	0.195526	0.243993	intron-variant	RNF157	GRCh38.p7	17:76190168	CTAACTGCTTGCTCT[C/T]TCTTTTTTTTTTTTT	114804
rs200290742	snp	C/G/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76210396	CAGATCGAGACCATC[C/G/T]TGGCTAACACAGTGA	114804
rs200375432	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76224716	TGATAGCTGATAAGC[-/T]TTTAAAAAAAAAAAA	114804
rs200383469	in-del	-/CA	0.00874735	0.0655527	intron-variant	RNF157	GRCh38.p7	17:76194002	ATGGGAACCAGGCCA[-/CA]GAGAAGGCAATCACA	114804
rs200506328	snp	A/G	4.52878e-05	0.00475835	missense, intron-variant, utr-variant-3-prime, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145269	CACACACAGGGCCTC[A/G]TCTCAGAGTCCTCCA	114804
rs200531961	in-del	-/TT	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76169359	AAAGAAAAAGATAAC[-/TT]CTCTCATGTCTTTGA	114804
rs200595190	snp	C/T	1.65261e-05	0.0028745	intron-variant	RNF157	GRCh38.p7	17:76155209	AAGGCCAGCACTCCT[C/T]TGGTTGTGGGAAGGG	114804
rs200604285	in-del	-/CA			intron-variant	RNF157	GRCh38.p7	17:76198278	GAGAGCCTGTTGATA[-/CA]GGGACATTCTCTTAT	114804
rs200733901	snp	C/T	6.69624e-05	0.00578591	intron-variant	RNF157	GRCh38.p7	17:76161811	TTGTCCCCTCTCCCA[C/T]CCACCAGTCCCCCTG	114804
rs200741033	snp	G/T			utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76143461	CTTCTGGGCTCATAT[G/T]TCAGGGAAATCAGGA	114804
rs200766102	in-del	-/GA	0.0138799	0.0821421	intron-variant	RNF157	GRCh38.p7	17:76230551	TATTTCTTAAAAGGA[-/GA]TACTGAGCCGGGCAT	114804
rs200806844	snp	C/T	6.6599e-05	0.00577019	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76162623	AGCTGACCCCGTCTA[C/T]CTGAACAGCAAACAG	114804
rs200852884	snp	C/T	0.00199792	0.0315431	intron-variant	RNF157	GRCh38.p7	17:76166989	GTGGATGTGGGAAAC[C/T]CTCCCCAGAGGCAGC	114804
rs200921693	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76164653	GAGCAAAAAGTAAAA[A/C]AAAAATAAAAAAAGA	114804
rs200960067	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76232245	TTTAAAAAATTAGAT[G/T]GGAGTGGTGGCATGT	114804
rs200968669	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76173224	CCTGGAGATGGAGCG[C/T]GCAGTGAGCCGAGAT	114804
rs200973612	in-del	-/G	0.0225045	0.103662	intron-variant	RNF157	GRCh38.p7	17:76173155	GCCGGACGTGGTGGC[-/G]GGCGCCTGTAGTCCC	114804
rs201021077	in-del	-/T	0.0103295	0.0711199	intron-variant	RNF157	GRCh38.p7	17:76160838	ATAATTTATTCTAGA[-/T]TTTTGAATGTTTTGC	114804
rs201057176	in-del	-/T	0.0325976	0.123435	intron-variant	RNF157	GRCh38.p7	17:76204213	GCACACTTCTGCATC[-/T]TTATGCTTCCTTGTA	114804
rs201096545	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76220657	TACAAATTTATTATT[-/A]TTTTTTTTTTTAGTT	114804
rs201166756	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76230862	AAAAAAAAAAAAAGA[A/G]AGAGAGAGAGAGAGA	114804
rs201169092	in-del	-/C			intron-variant	RNF157	GRCh38.p7	17:76236874	CAGAGCAAGGTGTAG[-/C]AACAGTCTAATAGCA	114804
rs201177780	in-del	-/T	0.0142736	0.0832652	intron-variant	RNF157	GRCh38.p7	17:76225458	GTGTGGCCTTCCAGA[-/T]TTTTTTTATACATAT	114804
rs201216172	in-del	-/AT			intron-variant	RNF157	GRCh38.p7	17:76215556	AAAAAAAAAAAAAAA[-/AT]GAGATTCAGTACTTT	114804
rs201284078	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76189839	GAGAACACAAACAAA[A/C]ACAACTGAAGGCTGA	114804
rs201287104	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76176505	TCGAAATTTCTTAGT[C/G]AGTTATCTTCCTTTC	114804
rs201291632	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76228942	TAATAATAATAATAC[-/A]AAAAAAAAAAATTCA	114804
rs201297855	in-del	-/A	0.0603597	0.1629	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152554	CTTAAGGATGGAGAC[-/A]AAAAAAAATCAAATC	114804
rs201316866	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76224390	AATTAAACCCATTTT[C/T]TATTCTTCTACAATT	114804
rs201329858	snp	C/T	1.64836e-05	0.0028708	intron-variant	RNF157	GRCh38.p7	17:76161521	GAGGGGCCGTGGTTC[C/T]GAGCCCAACTTACTG	114804
rs201446722	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76209079	GTTCTTTTTTTTTTT[-/T]AAGTGGCATTTATTG	114804
rs201484764	snp	A/T			intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76154754	CTAGGGCTCTCACTG[A/T]GAGCTGGCGTTCCAC	114804
rs201495655	snp	A/C/T	0.000396584	0.0140768	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76158479	CCTCTTCATGCAGCA[A/C/T]GGAAGAGTTTTGGGA	114804
rs201501148	snp	A/T	0.000363024	0.0134678	intron-variant	RNF157	GRCh38.p7	17:76155243	ACCACTCCGTGCTGT[A/T]GGGGTTACCTCTGCA	114804
rs201544317	snp	A/G	0.000136398	0.00825713	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76173758	TCTCAGAGTCTTCAC[A/G]GGTTCTTGGGGAGGT	114804
rs201554229	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76210601	TCCAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA	114804
rs201569768	snp	A/G	0.000199863	0.00999459	intron-variant	RNF157	GRCh38.p7	17:76161829	ACCAGTCCCCCTGCC[A/G]CTCTGGGGCTTACGC	114804
rs201615839	in-del	-/TAAA			intron-variant	RNF157	GRCh38.p7	17:76186983	AAATAAATAAATAAA[-/TAAA]ATCTCAACTCTGGTT	114804
rs201646108	snp	C/T	0.000408893	0.0142926	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155639	CTTCAGTGCCAGGGG[C/T]GATGTAGGAGCCAGA	114804
rs201662506	snp	A/G	0.000121048	0.00777878	missense, intron-variant, utr-variant-3-prime, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145306	TGGATGACAAGCGCC[A/G]GCGCTGGGCATTCCG	114804
rs201704419	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151555	TTCTGTCGTGAAACC[C/T]GGAGGGGACATTTGA	114804
rs201729868	in-del	-/AAAG	0.0217236	0.101931	intron-variant	RNF157	GRCh38.p7	17:76224729	AGCTTTAAAAAAAAA[-/AAAG]AAAGAAACTGCAAAA	114804
rs201739916	snp	C/T	0.000167566	0.00915178	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76173726	CTCAGTGTGTCCTTT[C/T]GGATATTGACCAGGC	114804
rs201798498	snp	C/T	4.97104e-05	0.00498525	intron-variant	RNF157	GRCh38.p7	17:76167152	AAGTGGGAGGCAAAG[C/T]AAAAGTCAGTATCCG	114804
rs201880630	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76210394	GTCAGATCGAGACCA[C/T]CCTGGCTAACACAGT	114804
rs201884585	in-del	-/CAAA	0.0142736	0.0832652	intron-variant	RNF157	GRCh38.p7	17:76219809	GCGAAAAATATATCT[-/CAAA]CAGTTTACAGTAATC	114804
rs201909046	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76202132	CTCTCTCTCTCTCAC[A/T]CACACACACACACAC	114804
rs201953508	in-del	-/T	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76169426	TTGTTTCCAATTAGA[-/T]TTTTTTTTACTTTAT	114804
rs202026911	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76216890	TGTGTCAAAAAAAAA[-/A]CAAAAACAAAAACAA	114804
rs202036436	in-del	-/AAAC	0.00835141	0.0640778	intron-variant	RNF157	GRCh38.p7	17:76216916	AAAAACAAAAACAAA[-/AAAC]AAACAAACAAACAAA	114804
rs202044605	snp	C/G	0.000626487	0.0176876	intron-variant	RNF157	GRCh38.p7	17:76166995	GTGGGAAACCCTCCC[C/G]AGAGGCAGCTCACCT	114804
rs202076401	in-del	-/AGTCTA			intron-variant	RNF157	GRCh38.p7	17:76236878	AGCAAGGTGTAGAAC[-/AGTCTA]ATAGCATGCTATGCT	114804
rs202077727	in-del	-/C			intron-variant	RNF157	GRCh38.p7	17:76204785	TTTCTTTCTTTCTTT[-/C]TTTTTTTTTTTGAGA	114804
rs202113418	in-del	-/C			intron-variant	RNF157	GRCh38.p7	17:76198281	GCCTGTTGATACAGG[-/C]GACATTCTCTTATGA	114804
rs202231879	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156349	GGGGGACACAACAGG[A/G]CATGGAGCAAGCGCC	114804
rs202236231	snp	C/G	0.00395087	0.0442699	intron-variant	RNF157	GRCh38.p7	17:76173674	AAGGAAGGTGCCTGG[C/G]ACCTGGCCCCAGCCT	114804
rs267605059	snp	A/G			missense, utr-variant-5-prime, nc-transcript-variant	RNF157	GRCh38.p7	17:76212426	ACAGGTAACCTTCAG[A/G]ATGAGTTGAGTCAAA	114804
rs367552555	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76209515	TAGCTCATCAGCTAT[C/T]GTTACTGCTAGTGTA	114804
rs367565781	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76223598	TAACCATATAAAACC[C/G]AAATTTTTTTCTTTC	114804
rs367566896	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76178230	CTGCCCAAGCCAGGG[A/C]TATGACTTCCTCTTT	114804
rs367585332	snp	G/T	6.71693e-05	0.00579484	intron-variant	RNF157	GRCh38.p7	17:76159603	GACAGGTTGAAAAAT[G/T]AATTAGGTCCTTTTT	114804
rs367643568	snp	A/G	1.65957e-05	0.00288055	intron-variant	RNF157	GRCh38.p7	17:76161656	CGGAAGGCTGTGAAG[A/G]AGAAAACAGGCAATC	114804
rs367702448	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76203784	CTTTTTTTTTTTTTT[C/T]TGGGACGGAGTCTCG	114804
rs367719734	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76220925	ATTGCGCCATTGTAC[C/T]CTGACCTGGGCAATA	114804
rs367723900	snp	C/T	0.000412531	0.014356	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76158438	AGAGAGCTGTGTCTC[C/T]GACTCGCTGCAGGAA	114804
rs367726427	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76184851	CCATTTATAGTCTTC[A/G]AACTCCTCTGCTAGG	114804
rs367766578	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76229111	CTCACACTTCATTTA[C/T]CTCTGCAGAATTCAA	114804
rs367790370	snp	C/G	0.00676609	0.0577691	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76154780	TCCACAGCACACCAT[C/G]GTCAGGGCACGTCTC	114804
rs367805853	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76165312	ATTTTTTTTGAGACA[G/T]AGCCTCACTCTATCG	114804
rs367822706	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76203731	TGCTGGGATTACAAG[C/T]ATGACCCACCACGCC	114804
rs367831543	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76218330	GCCCCTGAGCTCATC[G/T]GAGGAGTCTACTAAG	114804
rs367846319	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76174657	TCAAGAAGAGTCTAC[C/T]TCCATAGTGTGGTAT	114804
rs367860484	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76228033	TCTTTACAGTTTATG[C/T]TGCTTCCTGTTTTTT	114804
rs367862624	in-del	-/AAT	0.0626037	0.165477	intron-variant	RNF157	GRCh38.p7	17:76216592	CTCTGTATATTTAAA[-/AAT]AATAATAATAATAAT	114804
rs367884413	snp	A/G	0.000153988	0.00877328	missense, intron-variant, utr-variant-3-prime, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145248	GCTCAGACAGCCAAA[A/G]GGCCCCACACACAGG	114804
rs367900542	snp	A/G	1.85568e-05	0.00304599	synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145331	ATTCCGACTGACGGC[A/G]TTGTCATCAGCCTGC	114804
rs367937489	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76232337	ACGCTGCAGGGAGCT[A/G]TGATCGCACCACTGC	114804
rs367948176	snp	A/G	1.66463e-05	0.00288494	intron-variant	RNF157	GRCh38.p7	17:76167835	TTTGCAGAGTAGCAT[A/G]TCAATATTTTAAAAT	114804
rs367974435	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76158087	CCATCAGGCACACAT[A/G]TATTTTTTTACCTAT	114804
rs367983871	snp	A/T	0.000581903	0.0170474	intron-variant	RNF157	GRCh38.p7	17:76173659	CCCCCAGCCTCCCCA[A/T]AGGAAGGTGCCTGGG	114804
rs368001212	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76215418	AGTTCAAGGTTGCAG[C/T]GAGCTATGATTGCCA	114804
rs368009265	in-del	-/TGGCCCCGGCCC			intron-variant	RNF157	GRCh38.p7	17:76177139	CACTGGCCCCGGCCC[-/TGGCCCCGGCCC]AGTGAGGACCTGGAG	114804
rs368049637	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76160241	TGTCTAACACATCCT[A/G]TTGTAAACAAGTTTT	114804
rs368051159	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76209914	ACAGGCTCACACCAC[C/G]ACGCCCAGCTAATTT	114804
rs368056088	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76169883	ACCGCACCTGGCCTA[C/G]TTAGGTTGTTTTAAA	114804
rs368107607	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76227437	ATAATCTCTTCAGAG[A/G]ACTGACTCTATAACA	114804
rs368112306	snp	A/G	0.0142736	0.0832652	intron-variant	RNF157	GRCh38.p7	17:76235237	GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC	114804
rs368141900	in-del	-/TCTATT			intron-variant	RNF157	GRCh38.p7	17:76224389	CAATTAAACCCATTT[-/TCTATT]CTTCTACAATTCTAT	114804
rs368185934	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76218930	CAGAGCAAGACTCCA[A/T]CTCAAAAAAATAAAA	114804
rs368187765	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76185595	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	114804
rs368200081	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76237295	CCGTCATTACAAGGA[C/T]AGATGATGGTGCTTC	114804
rs368295702	snp	A/G	2.39398e-05	0.00345967	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76173782	GGGAGGTGGGGCGGC[A/G]TAAGGAAACTGTGTC	114804
rs368304058	snp	C/T	1.64768e-05	0.00287021	missense, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154322	CTTCCTCTATAACAT[C/T]ATTTCCCTAGGACAG	114804
rs368364997	snp	A/G	1.64776e-05	0.00287028	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161590	GGGTTAAAGCTGGTT[A/G]GGGACAAGGGGCCCA	114804
rs368390165	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76209122	AGATGGAGGTCTTGC[C/T]ATATTGCTCAAACTG	114804
rs368400890	snp	C/T			upstream-variant-2KB	RNF157	GRCh38.p7	17:76241615	TATTTTGTTTTTGTT[C/T]TTCTGTGTTTTGAGA	114804
rs368449822	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76170506	TGTCCAGAGATTCTC[C/T]GTTTTGACCTTTCCA	114804
rs368464660	snp	C/T	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76237871	GGATCACCTGAGAGG[C/T]CAGGAGTTCAAGACT	114804
rs368470200	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76219915	TTATCATACCTAGCG[C/T]ATTGAGAATCAGAGA	114804
rs368484011	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76205031	ACCTCAAGTGATCCA[A/C]CTGCCTCGGTGTCCC	114804
rs368491934	snp	A/G	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76210339	TGGCTCATGCCTGTA[A/G]TCCCAGCACTTTGGG	114804
rs368504591	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76232874	ATCTTTCCATGTGTT[A/C]ATCAGCCATTCCTAC	114804
rs368526516	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76239453	CCACTCCAAAACCCA[C/G]GCTTGCCACTACGCT	114804
rs368606009	snp	A/C/T			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76148089	TTAGTGCCCACAAAG[A/C/T]GCAAGTAGCATCTTA	114804
rs368642441	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76176222	CATAGTAATTGTAAT[A/G]TCAAAGAGATTAAAT	114804
rs368701822	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76233914	CAATCCAATGGTTTT[C/T]AGTATATTGACCGTG	114804
rs368712952	snp	G/T	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76174404	TTTACCATCCGCTTC[G/T]TCCCCCTTTGCCCGT	114804
rs368722076	snp	G/T	0.000181811	0.0095327	intron-variant	RNF157	GRCh38.p7	17:76158372	TACAACACCCAAGAA[G/T]AGGAGAGGAATGTCA	114804
rs368723809	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76172989	ACATGATATAGGGAA[C/T]AAAAAAGAAAAAGAA	114804
rs368756329	snp	A/G	1.85122e-05	0.00304233	intron-variant	RNF157	GRCh38.p7	17:76162509	ACGATTTCTCACTTG[A/G]CCTCCTGGAAAGAGT	114804
rs368758814	snp	A/G			upstream-variant-2KB	RNF157	GRCh38.p7	17:76240974	AGCCTTCCCAACCCC[A/G]CCCCTCAGCGTCGGC	114804
rs368763224	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76225086	CTGAGGCAGAAGAAT[C/T]GCTTGAACCTGGGAG	114804
rs368794414	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76156885	GATGCAAAGTTCTAC[A/G]AACTGTATCTCCATA	114804
rs368827454	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213704	GGTCACTGGAAAGAA[A/G]AGGCAGGATTAGAGG	114804
rs368851236	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76162403	CCAAAGTGGTAAAAG[C/T]GTAATGATCTGAAAT	114804
rs368877190	snp	A/G	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76194876	AAAAATTAGCCAGGC[A/G]TGGTGGCGGGCGCCT	114804
rs368915312	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76225519	ATTTTTTTTAATTGA[A/G]TGGACTATTTGAATG	114804
rs368916655	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76194162	CAACAGTGTAACCAC[C/T]ATTACAAACAAAATA	114804
rs368978170	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76176840	CTTCAGGGGCCCCGG[A/G]CAGGAAGTGGGAGCA	114804
rs369012558	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76238239	CCGTCTAGAGCATAT[A/G]TGCAAGCTCACATAA	114804
rs369073980	snp	C/G/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142940	GGAGAAGCCAGGCCC[C/G/T]ACCTCTTCTCTTTGG	114804
rs369102696	snp	C/T	0.000101798	0.00713364	intron-variant	RNF157	GRCh38.p7	17:76166993	ATGTGGGAAACCCTC[C/T]CCAGAGGCAGCTCAC	114804
rs369108157	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76233293	TAATATTGATACACA[A/T]CCTTTATGTGATTTG	114804
rs369110536	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76202733	AAAAAGTGGCCAATC[C/G]AGGCTTCAAACAAGT	114804
rs369130453	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76166974	CCTAGGCCCTTCTGA[C/G]TGGATGTGGGAAACC	114804
rs369244581	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76216900	TGTGTCAAAAAAAAA[A/C]AAAAACAAAAACAAA	114804
rs369273266	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76186367	AAAAAATTAGCTGGG[C/T]GTGGTGGCGGGTGCC	114804
rs369281426	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76156670	TCAGCTTTCCTTCTG[C/T]GGCAAAAGCATACAA	114804
rs369282347	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150434	GCTGGAGGGAGTCAG[A/G]AAGAGGAGGAATAAG	114804
rs369287373	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76171933	ATGGTCTCCATCAAA[C/T]GTGTGAATGTGCCAT	114804
rs369291292	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76186940	ATGAGACTCCGACTC[A/T]AAATAAATAAATAAA	114804
rs369319423	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76225694	AATTTATTGGAACAC[A/T]CAGCTACAGCAGACA	114804
rs369332258	snp	C/T			intron-variant, downstream-variant-500B	RNF157	GRCh38.p7	17:76156066	TAGGAAAGCAAGTCC[C/T]CTTCCCTCTCAAGCC	114804
rs369363874	snp	A/G	3.30355e-05	0.00406407	intron-variant	RNF157	GRCh38.p7	17:76155225	TGGTTGTGGGAAGGG[A/G]GCACCACTCCGTGCT	114804
rs369383458	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76201312	GCAACATAGTGAGAC[C/T]CTAGTCTCTACAAAA	114804
rs369390338	snp	C/T	0.00636936	0.0560724	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144624	GAGCTCCTTCTTAAC[C/T]GCACAGGCATGTGAG	114804
rs369390466	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76167319	CCACACATCCAAAGA[A/T]AGGTAGCTTACTAGA	114804
rs369397286	snp	C/G	0.0023933	0.0345097	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76148046	AGTTGCTCTCCAGGG[C/G]AAGGAGAAACTTAGT	114804
rs369416332	snp	A/T	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76222166	GCCTGGCCAACATGA[A/T]GCAACCCCGTCTCTA	114804
rs369492937	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76228704	GAGGCAGATGAATCA[C/T]CTGAGGTCAGGAGTT	114804
rs369505795	snp	A/G	0.000153988	0.00877328	stop-gained, nc-transcript-variant	RNF157	GRCh38.p7	17:76167077	GCTGACACACTCCTC[A/G]CTTGTACTGCACAGT	114804
rs369511766	snp	C/T	0.000235905	0.010858	intron-variant	RNF157	GRCh38.p7	17:76155547	AGCCAGGGCGGTTCC[C/T]GTCCCTTCCCTTACC	114804
rs369539256	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76168538	TCAGATGCACCAAGC[G/T]GTCTATTCATTTCAT	114804
rs369621852	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76175546	CTCCTCCCCCAACTT[G/T]CCTAGGCTGTCATAC	114804
rs369629222	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76217237	CTGGTCTCAAACTCC[C/T]GGGTCAAGAGACCTG	114804
rs369663286	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76232615	TGGACAGATTCATAG[C/G]AGTGGAACTGCTGAA	114804
rs369683235	snp	A/G	0.000153988	0.00877328	intron-variant	RNF157	GRCh38.p7	17:76155246	ACTCCGTGCTGTTGG[A/G]GTTACCTCTGCATCC	114804
rs369704714	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76229570	TCCAAATCTTCAATC[A/C]CCTGCCATATCTTTT	114804
rs369723866	snp	A/G	0.000101163	0.00711136	intron-variant	RNF157	GRCh38.p7	17:76162011	CAGCCACCTGGCCAA[A/G]GAGAAAGAAATGTAG	114804
rs369739949	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76180121	AGAAGCTTTCTGATC[G/T]CTTACCTCAAGCTCA	114804
rs369814303	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76240119	GCCCCTGCCCCTCTC[C/T]CTCCTCGCGGCTGCG	114804
rs369823481	snp	A/T	0.000153988	0.00877328	intron-variant	RNF157	GRCh38.p7	17:76166567	AAAAAAAAGAGGACT[A/T]AACACATTTACATGG	114804
rs369863786	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76176492	CCTACTATTACTCTC[A/G]AAATTTCTTAGTGAG	114804
rs369870242	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76197822	TGAACTCTCAGCCTA[C/T]ACTAGTCTACTGTGC	114804
rs369940307	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150866	CCAGCAAGCTTGGAC[A/G]GGGTGAAGCATTGGC	114804
rs369948966	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76191580	CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCC	114804
rs369954761	snp	C/T	0.000913189	0.0213485	intron-variant	RNF157	GRCh38.p7	17:76159302	TTTCATCAAGGATTC[C/T]GGGGGCAACAGTGTG	114804
rs370029658	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76167297	ACGTTAAACTTTTCT[A/G]TTCAACCCACACATC	114804
rs370045755	snp	A/C/G			intron-variant	RNF157	GRCh38.p7	17:76229944	AAACTTTAAAGTACT[A/C/G]TTTAGGGTAACCATG	114804
rs370047752	snp	C/G	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76203612	AACCCGCCATCATGC[C/G]TGGCTAATTTTTGTA	114804
rs370158166	snp	C/T	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76200228	GCCTGGGCGACAGAG[C/T]GGGACTCCGTCTTGT	114804
rs370229370	snp	A/G			upstream-variant-2KB	RNF157	GRCh38.p7	17:76241094	GTGACCGGCTAGGAA[A/G]ATGCCGCCTCCCTCT	114804
rs370254190	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76170226	CAGTATGCCAGGATC[C/T]ACTCACCTGCTGTTT	114804
rs370275310	in-del	-/TT			intron-variant	RNF157	GRCh38.p7	17:76168429	TAGTGCTCATCCTAT[-/TT]TTTTTTTTTTTTCTT	114804
rs370280736	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76183530	TATTCACTGTGACCA[C/T]AGTGCACTACAGCCT	114804
rs370293245	snp	A/G	1.6483e-05	0.00287076	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167783	TCTCCAGGGCTCTTC[A/G]CTTCCTCAGCACATC	114804
rs370428157	in-del	-/AACA			intron-variant	RNF157	GRCh38.p7	17:76219811	GAAAAATATATCTCA[-/AACA]GTTTACAGTAATCAT	114804
rs370435455	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76189044	AAATTTTCAAGGTCA[G/T]GAAGAACAAGGAAAA	114804
rs370450153	snp	A/G	0.0023933	0.0345097	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76148471	ATGAGGTTTCACCGT[A/G]TTAGCCAGGATGGTC	114804
rs370455768	snp	C/T	1.64953e-05	0.00287182	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159477	GGCCATCTCCAAGCA[C/T]GTGAAGTGGAGGAAC	114804
rs370472621	snp	A/G	5.02769e-05	0.00501358	intron-variant	RNF157	GRCh38.p7	17:76162643	ACAGCAAACAGAAAG[A/G]TTCAAGGACAGGCTG	114804
rs370503920	snp	A/G	0.000153988	0.00877328	missense, intron-variant, utr-variant-3-prime, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145329	GCATTCCGACTGACG[A/G]CATTGTCATCAGCCT	114804
rs370578047	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194797	AAGGTGGGCAGATCA[C/T]GAGGTCAGGAGATCG	114804
rs370597314	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76164612	ATTAAAAAAAAAAAA[-/A]GAGGAAAAGGAGAGA	114804
rs370610143	snp	A/G			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153892	CTCCCCCTCCCCCCA[A/G]TGGAAGAAATGGCTA	114804
rs370634395	snp	A/G	0.188316	0.242271	intron-variant	RNF157	GRCh38.p7	17:76210483	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	114804
rs370701115	snp	A/G/T	6.62497e-05	0.00575509	intron-variant	RNF157	GRCh38.p7	17:76161496	AAAAGCCAATGAGGC[A/G/T]TTTGCTTCAGAGGGG	114804
rs370706670	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76231015	CAGATCATAGTCCAC[C/T]GCAGCCTTGACCTCC	114804
rs370716524	in-del	-/C	0.00398564	0.0444627	intron-variant	RNF157	GRCh38.p7	17:76200250	CGTCTTGTCAAAAAA[-/C]AAAAACAAAAACAAA	114804
rs370725606	snp	A/G	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76165339	ATCGCCCAGGCTGGA[A/G]TGCGGTGGTGCCATC	114804
rs370733681	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76237069	AACCGTGTGACTATA[C/T]TACCTATTCAAAAAT	114804
rs370734970	snp	G/T			upstream-variant-2KB	RNF157	GRCh38.p7	17:76241256	GACCCCGGAAACTTT[G/T]GAAAGGCCTGAGTGC	114804
rs370749605	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76217839	ATTAATCAAAACTCA[C/T]ATTCAGAATTCTTTG	114804
rs370809039	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76210831	TTTTTTTGAAACAGA[A/G]TCTCATTCTATCCCC	114804
rs370857000	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76203654	ACGGGGTTTCACCAC[A/G]CTGGCCAGGCTGGTC	114804
rs370862027	snp	A/G			intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147545	CAGGGCAGAACATCG[A/G]TTACTTGTGGAAGAC	114804
rs370876146	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76190458	AGGTGTGAGCCACTG[C/T]GCTTGGCCATTCTCT	114804
rs370982681	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76161335	CACCAAGTTCCCAAG[A/G]AGGAAAAGGGAGGTT	114804
rs371016270	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76199403	CTGGGACTATAGGCA[C/T]GCTCCATCATACACA	114804
rs371022643	snp	A/G			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76214353	TGTATAGGAGAAACT[A/G]AGTTTTTTTCCTATA	114804
rs371024273	snp	C/T			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213961	CCTCGCCCTATGTAT[C/T]TCTCTCTGTATCCTT	114804
rs371049943	snp	C/T			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145581	TACAGTCACTGCCAC[C/T]GTGGCTCCCGGACAG	114804
rs371050745	snp	C/G	1.65181e-05	0.00287381	synonymous-codon, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156244	GGATGACAGAGGCGT[C/G]CCTGTGCAAGACGAC	114804
rs371151310	snp	C/G	3.36146e-05	0.00409953	intron-variant	RNF157	GRCh38.p7	17:76155359	CTCTTCCATAAAGGT[C/G]TCGTGACAGCAAACC	114804
rs371168111	in-del	-/G			intron-variant	RNF157	GRCh38.p7	17:76202347	CCTCTCACAGAGGCT[-/G]GTTCCTTGGAGTGTC	114804
rs371195412	snp	C/T	0.00874735	0.0655527	intron-variant	RNF157	GRCh38.p7	17:76194831	CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT	114804
rs371217323	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76174076	CTGGAGAATTAATAA[-/T]AAAAAAAAAAACCGC	114804
rs371220040	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76174524	CTGAGGATCAAGAAT[C/G]ATTTCAAATGTTCCC	114804
rs371221367	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76226436	TCCTGGACTAGGGGG[A/G]CAAAGAGATTACAAG	114804
rs371227634	snp	C/T			intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153478	CGTCTGTATCCAGGC[C/T]GGGCATACGTGTGCT	114804
rs371237589	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76220882	AGAATCACTTGAACC[A/G]GGGAGGCAGAGGTTG	114804
rs371288986	snp	C/T			upstream-variant-2KB	RNF157	GRCh38.p7	17:76241065	CGCATGTCTCCTGCC[C/T]CGTGTTAATGCTGGT	114804
rs371302209	snp	C/G	0.000153988	0.00877328	missense, utr-variant-5-prime, nc-transcript-variant	RNF157	GRCh38.p7	17:76212403	GTTCAGATCGCTGTT[C/G]TCTCCAAACAGGTAA	114804
rs371326674	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76172142	ATAGCTGGGGAACCA[A/G]CAGAAACTTCAGGGA	114804
rs371359282	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76210932	GCTTCAGTCTCTGGA[G/T]CAGCTGGGATTATAG	114804
rs371381620	snp	C/G/T	3.29806e-05	0.00406071	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161623	TTTTTCCTCATGGCT[C/G/T]GGATCTGAAGCAGTG	114804
rs371393248	in-del	-/CT			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76148295	TTTGAGACAGGGTCT[-/CT]TGCTCTGTCGCCCAG	114804
rs371409147	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76178464	ACACCCCTTGCTGCT[C/G]CATGCCTGACTTGCA	114804
rs371417096	in-del	-/CTC			intron-variant	RNF157	GRCh38.p7	17:76190168	CTAACTGCTTGCTCT[-/CTC]TTTTTTTTTTTTTTT	114804
rs371431479	snp	A/T	1.67349e-05	0.0028926	intron-variant	RNF157	GRCh38.p7	17:76161687	AGGACATCCTGATAC[A/T]GGATTAAGAATGAAC	114804
rs371431924	snp	C/T			missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167672	ATACCATTCTGGAAC[C/T]CTTCCGTGGCCTGGT	114804
rs371437378	snp	A/G	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76184121	ACTTGAACCTGGGAG[A/G]CAGAGGTTTCAGTGA	114804
rs371557949	snp	C/T			utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144763	GGGAAACGCTACGTC[C/T]GTGCAGTATGGCTCT	114804
rs371599762	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76195085	AAACTTGGAAGCTGA[A/G]ACACACACTGACAAG	114804
rs371604772	snp	C/T			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212659	CTGAGATAAGGAGTT[C/T]GAGACCAGCCTGGCC	114804
rs371622346	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76176655	ACAGCTTGCCGCCCT[A/G]GAGGCCACCCCATGG	114804
rs371623883	snp	C/T	3.30393e-05	0.0040643	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76158470	GCTCATCTTCCTCTT[C/T]ATGCAGCACGGAAGA	114804
rs371701536	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76155174	CCTCCTGGCCCTGGT[C/T]CTTACTGGCATCCCC	114804
rs371713656	snp	C/T	1.64928e-05	0.00287161	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76161871	GGGGCAGTTGTTGGC[C/T]TGGTAGCGCAGCGTG	114804
rs371753613	snp	C/T	0.000153988	0.00877328	missense, intron-variant, utr-variant-3-prime, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145252	AGACAGCCAAAGGGC[C/T]CCACACACAGGGCCT	114804
rs371758551	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76152075	GGTACCTGCAAGGCC[A/G]TGATGTGGGGTGGAG	114804
rs371809616	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76200391	GGCATATTATTCAGC[C/G]TTAAAAAGGAAATTC	114804
rs371830946	snp	A/G	9.8974e-05	0.007034	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76159412	CGAGATCGTCCTGAC[A/G]GGGGGCAGGTGGCCA	114804
rs371835725	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76197872	GAAGGAGTGAACTCT[-/T]AAGACTTGAGATGGG	114804
rs371836411	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76224023	TCAGCACTTTCTGGC[A/T]CTACAAGAACTCAGG	114804
rs371847479	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76239542	TCCACCACCACCACC[A/C/G]CCCCCACCCCCCGGC	114804
rs371921633	in-del	-/AAAT/AATAAATAAAT	0.00874735	0.0655527	intron-variant	RNF157	GRCh38.p7	17:76186940	TGAGACTCCGACTCA[-/AAAT/AATAAATAAAT]AAATAAATAAATAAA	114804
rs371976538	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76206151	TGGGAGGATCACTTA[A/C]GCCTAGGAAGTCGAG	114804
rs372035076	snp	C/T			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213007	ATACCAAACGTAGAC[C/T]AGATCACTGTTTTCC	114804
rs372058550	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76175950	GAAAGGTATCAATGA[A/G]TTCAATTGTTTATAA	114804
rs372059938	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76232407	AAAAAAAAAGCAAAG[A/G]AACAAACAAAAAATT	114804
rs372077924	snp	C/T	1.64838e-05	0.00287083	intron-variant	RNF157	GRCh38.p7	17:76166423	TATGCCACAAAAGAG[C/T]AGTGTGCACAGCCAA	114804
rs372094411	snp	A/G/T	6.59417e-05	0.0057417	intron-variant	RNF157	GRCh38.p7	17:76166453	AAGAGGACAGAAATC[A/G/T]CCCCTACCGTCTCCT	114804
rs372102015	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76232400	TCTCTAAAAAAAAAA[-/A]GCAAAGAAACAAACA	114804
rs372125798	snp	A/G	5.60952e-05	0.0052957	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145383	ATGAACATTACAGGA[A/G]CCAGACCTTTGGCCA	114804
rs372149797	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76224997	GCCAACATGGTGAAA[C/T]CCTGTCTCTACCAAA	114804
rs372177156	snp	C/T	6.78372e-05	0.00582357	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76173754	GGCTTCTCAGAGTCT[C/T]CACGGGTTCTTGGGG	114804
rs372257769	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76206706	GGACTGCAATGGCGT[C/G]ATCTTGGGATCTCGG	114804
rs372260610	snp	A/C	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76190748	CCGTCTCTACTAAAA[A/C]CACAAAAAATTAGCC	114804
rs372285040	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76223542	TCCTGTACTGTAATA[A/G]GAAAAAAGAAAGAGG	114804
rs372287219	snp	A/C	0.00478085	0.0486577	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76148377	GTTCACGCCATTCTA[A/C]TGTCGCAGCCTCCTG	114804
rs372327349	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194878	AAATTAGCCAGGCGT[A/G]GTGGCGGGCGCCTGT	114804
rs372361516	snp	A/G	9.90851e-05	0.00703795	intron-variant	RNF157	GRCh38.p7	17:76158388	AGGAGAGGAATGTCA[A/G]TTACCTCTCCGAGAT	114804
rs372393474	snp	A/G	1.64901e-05	0.00287137	intron-variant	RNF157	GRCh38.p7	17:76165490	AAAGCGAGGCCCTCT[A/G]AAGTCACTCACCTTC	114804
rs372407742	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76166639	AATCTCATCTCTGCT[C/T]CTCATTCTTTAGCCT	114804
rs372436777	snp	A/G	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76237724	ATGGGAGGCCAAGGC[A/G]GGAGGATTGCTTGAG	114804
rs372461096	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76204715	TGAGTACAACTTTTG[A/G]TCTATCTGTACTAGA	114804
rs372519000	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76228964	AAAAATTCACTCACC[C/T]ACCCACTCACCCATC	114804
rs372585844	snp	A/C			upstream-variant-2KB	RNF157	GRCh38.p7	17:76241689	TCTCAGCTCACTGCA[A/C]CCTCCGCCTCCTGGG	114804
rs372599794	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76235925	GAGGCAGGAAGATCG[C/T]TTGAGCCCAGGACTT	114804
rs372667049	in-del	-/TTCT			intron-variant	RNF157	GRCh38.p7	17:76225607	ATACTGTAGGCATCT[-/TTCT]ATGTCTGTATTTATG	114804
rs372671322	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76181629	TGTTTTCAAAAAATG[A/G]TCGGGTGCGGTGGCT	114804
rs372709099	snp	C/T	1.6507e-05	0.00287284	intron-variant	RNF157	GRCh38.p7	17:76212325	TTTTTGAATTGGCCA[C/T]TTAAGCTCCAAGTAG	114804
rs372713587	snp	G/T	0.000153988	0.00877328	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154352	GAAGGAAGGCCCTGT[G/T]AGTCTATGAAGCGGC	114804
rs372744205	snp	C/G	0.00874735	0.0655527	intron-variant	RNF157	GRCh38.p7	17:76157140	CCTGGCTAATTTTTT[C/G]TATTTTTAGTAGAGA	114804
rs372746502	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76156814	CACACCCCCACCTCC[A/G]ATCCCAGCCCCGACC	114804
rs372749559	snp	A/C	0.000120485	0.00776067	intron-variant	RNF157	GRCh38.p7	17:76166962	TCCTAAGTAGCCCCT[A/C]GGCCCTTCTGAGTGG	114804
rs372758331	snp	A/G	0.00478085	0.0486577	intron-variant	RNF157	GRCh38.p7	17:76209201	CTCCTGAGTAGCTGG[A/G]ACCACAGGCACATGC	114804
rs372759286	in-del	-/GAGA			intron-variant	RNF157	GRCh38.p7	17:76230906	AGAAAGAGAGAGAGA[-/GAGA]CTTTTCTTAGATTAA	114804
rs372761404	snp	A/G	6.7382e-05	0.00580401	intron-variant	RNF157	GRCh38.p7	17:76155548	GCCAGGGCGGTTCCC[A/G]TCCCTTCCCTTACCT	114804
rs372842357	snp	A/C/G	1.65111e-05	0.0028732	intron-variant	RNF157	GRCh38.p7	17:76155236	AGGGGGCACCACTCC[A/C/G]TGCTGTTGGGGTTAC	114804
rs372866724	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76238009	GAATTGCTTGAACCC[C/T]AGAGGCAGAGGTTGC	114804
rs372895169	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76225819	TCAGGTACTGGATCT[C/T]CTTGGCCAGGGAATC	114804
rs372910206	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76176283	AAATAAAGGAAGTGA[C/T]CATTTCTGGCTGAGG	114804
rs372995401	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76201362	AAGAAAAAATTTTAA[A/G]TTAGCTGTGCATGGT	114804
rs373012762	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76225780	TCTTCCCCCTTGCCT[C/T]GCGGACCTCTTCTAT	114804
rs373056134	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167088	CCTCGCTTGTACTGC[A/G]CAGTCTCCGACTGGA	114804
rs373070817	snp	C/G	0.000153988	0.00877328	intron-variant	RNF157	GRCh38.p7	17:76162513	TTTCTCACTTGGCCT[C/G]CTGGAAAGAGTACAT	114804
rs373101987	snp	C/T			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76214085	AACCCTGCTTTCTGG[C/T]TGGTTAGTTGGAAGC	114804
rs373106945	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76207881	CATGGAATACGAACT[C/G]TGAAGAGGCGCTCCA	114804
rs373111194	in-del	-/GGCTG	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76235727	ATGTGATACATCTAT[-/GGCTG]GGTACGGTAGATCAC	114804
rs373131572	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76168613	CCTCTGCACCTGGCT[C/G]CCAGTCGCCACCCTG	114804
rs373160440	snp	A/G	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76210463	GGTGTAGTGGCGGGT[A/G]CCTGTAGTCCCAGCT	114804
rs373197051	snp	A/G			utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144673	GCCACCAGAAGGAAG[A/G]ATTGTTTCCTTCAAC	114804
rs373244691	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76176908	TGTGCCCACCCTGCC[A/G]AGGGTGCCAGGTTCC	114804
rs373250104	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76168056	AAAAGTTATTAATCA[C/T]ATAGTTTAAATAGTT	114804
rs373301935	snp	A/T			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152742	TGGGACACAGGCTCA[A/T]CAGAGAATACTAGAG	114804
rs373312575	in-del	-/AG			intron-variant	RNF157	GRCh38.p7	17:76236867	AAAGCAAACAGAGCA[-/AG]GTGTAGAACAGTCTA	114804
rs373314751	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76164390	AAATGTTTCTCACTC[C/T]GGCATTTTAAATAAA	114804
rs373315454	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76225427	CCATAAGAAGTAACT[C/T]CACTATTCACAATTG	114804
rs373322935	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76180976	GCCGGAGAAATACAG[C/T]AGCCGACTGAAAAAT	114804
rs373328080	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76235317	ATTCTCCTGCCTCAG[C/T]CTCCCGAGTAGTTGG	114804
rs373338112	snp	A/C/G	3.37446e-05	0.00410748	intron-variant	RNF157	GRCh38.p7	17:76166999	GAAACCCTCCCCAGA[A/C/G]GCAGCTCACCTCCTC	114804
rs373345194	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76216595	CTGTATATTTAAAAA[A/T]AATAATAATAATAAT	114804
rs373353975	snp	C/T	0.0558544	0.157504	intron-variant	RNF157	GRCh38.p7	17:76210462	GGGTGTAGTGGCGGG[C/T]GCCTGTAGTCCCAGC	114804
rs373375968	snp	C/T	4.95021e-05	0.0049748	intron-variant, missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155260	GGGTTACCTCTGCAT[C/T]CTGCTCTCCAGCTGG	114804
rs373407103	snp	C/G/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151136	GCTCCCTCCTCCACG[C/G/T]TCAGGCAGGAAGGGG	114804
rs373409131	in-del	-/GTTT			intron-variant	RNF157	GRCh38.p7	17:76194065	TTTTTTTGTTGGTTT[-/GTTT]ATCAAGGTATAATTT	114804
rs373427668	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76170813	AACAGCAACAACATT[G/T]TAGAAGCTGGAAACA	114804
rs373446266	snp	A/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150502	GCAGCTCCCTCTGCC[A/G]AAAAAATAGGGGTGG	114804
rs373455262	snp	C/T	0.000153988	0.00877328	intron-variant	RNF157	GRCh38.p7	17:76159316	CCGGGGGCAACAGTG[C/T]GGAGCACTGGCTACT	114804
rs373460814	snp	A/C	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76217335	TTAAAAGGAAAAATA[A/C]ATTTACTTATTGGTA	114804
rs373474778	snp	A/G	0.00318978	0.0398085	intron-variant	RNF157	GRCh38.p7	17:76181954	AATAATTTTCAAAAA[A/G]CAAAGACATTTACCC	114804
rs373490936	snp	A/G			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213818	AATCAACCATGCTAT[A/G]TAATGAAGCTTCTAT	114804
rs373548467	snp	C/T	0.00019983	0.00999376	intron-variant	RNF157	GRCh38.p7	17:76158537	AGCAGCTATATCCAA[C/T]GTCCATTTAAAGAAC	114804
rs373582825	snp	C/T	0.0023933	0.0345097	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76148164	TCAGGTCTCCACAAA[C/T]CTTTTTAGATTTCAC	114804
rs373613224	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159516	ACGGGGTGAGGGGCC[C/T]GTTGAGGGCCTCCAG	114804
rs373648758	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76183970	TGAGGTGGGCGGGTT[G/T]GTTGAGGCCAGGAGT	114804
rs373655527	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76218211	CCAGGCAAAAAGTCA[A/G]AATTCTAGAGGGGAA	114804
rs373663175	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76174584	AAAATGTTTTAACAT[A/G]TAATTCCCAAAAAAC	114804
rs373668247	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76194883	AGCCAGGCGTGGTGG[C/T]GGGCGCCTGTAGTCC	114804
rs373671675	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76211924	AGGGCTTAACATTAC[A/G]TGCCAGGCTTTGTTC	114804
rs373711178	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76227484	TACTACACGGGTTAT[C/T]CTTCACAACCCTTTG	114804
rs373753174	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76201349	AAAAAAAGAGAAAAA[A/G]AAAAAATTTTAAATT	114804
rs373781346	snp	A/G			intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76148716	TCTGGGACCACAGGC[A/G]TACGCCACCAAGCCT	114804
rs373845100	snp	C/G	0.000247142	0.0111135	intron-variant	RNF157	GRCh38.p7	17:76155747	GGCCTTTGGAGACAG[C/G]GGATGGGGAAAGGAG	114804
rs373847550	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76159845	AAGTAAGGAAAAAAA[A/G]TCACCAGTAATCAAA	114804
rs373896504	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76200236	GACAGAGCGGGACTC[C/T]GTCTTGTCAAAAAAA	114804
rs373905626	snp	A/G	0.000134944	0.00821302	intron-variant	RNF157	GRCh38.p7	17:76162012	AGCCACCTGGCCAAG[A/G]AGAAAGAAATGTAGC	114804
rs373939999	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76232296	GGGAGGCTGAGGCTG[C/G]AGGAGTGCCTGAGCC	114804
rs373983161	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76178835	CTCTCTTTTTTTTTT[-/T]CCAGTAACTAACATG	114804
rs374046104	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76165875	TAGAGACGGGGTTTC[A/C]CTATGTTGGTCAGGC	114804
rs374070094	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76234170	TTTCACTGAGTATAA[-/A]CATTTTCAAGGTTCA	114804
rs374098693	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76222527	ATAATGCTGTCATTT[A/G]AATTTTTATTTTAAC	114804
rs374124677	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76173143	TACAAAAAATTAGCC[A/G]GACGTGGTGGCGGGC	114804
rs374175077	in-del	-/TAA			intron-variant	RNF157	GRCh38.p7	17:76215312	AAAACAAAAAATAAA[-/TAA]AAATACAAAAATTAG	114804
rs374197253	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76162400	TTTCCAAAGTGGTAA[A/G]AGCGTAATGATCTGA	114804
rs374215088	snp	C/T	8.41744e-05	0.00648692	intron-variant	RNF157	GRCh38.p7	17:76155361	CTTCCATAAAGGTCT[C/T]GTGACAGCAAACCCA	114804
rs374224492	snp	A/G			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147635	GATCCGGCAGCAAGC[A/G]GGGGGCACCTTCCCC	114804
rs374258079	snp	A/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76165297	TTCTTTTATTTATTT[A/T]TTTTTTTTGAGACAG	114804
rs374268501	snp	A/C	0.00795532	0.062565	intron-variant	RNF157	GRCh38.p7	17:76171230	GTCTCACTCTGTCAC[A/C]CAGAGTGGAGTGCAG	114804
rs374286443	snp	C/T	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76203682	GTCTTAAACTCCTGA[C/T]CTAAGGTGACCTCCC	114804
rs374332739	snp	C/T	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76157111	AGCTGGGACTACAGG[C/T]GCATGCCACCACACC	114804
rs374342005	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76173696	CCCCAGCCTCTGGGA[A/G]CTTACTTGACGAGCC	114804
rs374396479	in-del	-/TC	0.487558	0.0778863	intron-variant	RNF157	GRCh38.p7	17:76202111	AACCCAATCTCAGTT[-/TC]TCTCTCTCTCTCTCT	114804
rs374455452	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76226653	CCGCCTTAGCCTTGT[C/T]GCTGGAGAACCCATG	114804
rs374504676	in-del	-/TGTG			intron-variant	RNF157	GRCh38.p7	17:76182452	CACACGCATTTAGTC[-/TGTG]TGTGTGTGTGTGTGT	114804
rs374532457	snp	C/G	1.66443e-05	0.00288477	intron-variant, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156326	ACACCACATTCCTGG[C/G]GGTTGTGGGGGGACA	114804
rs374546733	snp	A/G	2.29397e-05	0.00338664	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145202	TGGATGGAATGCAGG[A/G]CAGGAGGGGAGCCCA	114804
rs374549987	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76230949	TCTTTTTTTTTTTTT[C/T]TTTTTTAAAGTTAGG	114804
rs374567039	snp	A/G			intron-variant, nc-transcript-variant	RNF157	GRCh38.p7	17:76156477	CAGCTTCTCTCTTCC[A/G]TCCTCACTTCAGCCC	114804
rs374577488	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76176595	CCGCTGCCATCACAA[C/T]GGCTGCTGCAGGGGG	114804
rs374586349	snp	C/T	0.00478085	0.0486577	intron-variant	RNF157	GRCh38.p7	17:76215140	CTAAATCAGTTGCAA[C/T]TTTTGTTGAAGATTT	114804
rs374587545	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76198197	TGGCCAACAAAGGCA[A/C]TAGCAGGACCTGGAG	114804
rs374621483	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76200033	ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT	114804
rs374622547	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76209230	GCCACTGTGCCCAGC[C/T]TGATCTTCTTTGGGA	114804
rs374623424	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76230139	AGCAAACTGGATCAT[A/G]GGAGTCAAAATGATC	114804
rs374626701	snp	A/G	4.10602e-05	0.00453083	missense, intron-variant, utr-variant-3-prime, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145303	TGCTGGATGACAAGC[A/G]CCGGCGCTGGGCATT	114804
rs374639994	snp	C/T	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76158996	TTTAAGAGATACGGA[C/T]CACAAGGTTCCTTCA	114804
rs374650065	snp	C/T			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213344	GGAGGCTGAGGAGGG[C/T]GGATCACTTGAGGTC	114804
rs374665760	snp	C/T	1.64838e-05	0.00287083	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76167785	TCCAGGGCTCTTCAC[C/T]TCCTCAGCACATCTA	114804
rs374677840	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76220905	AGAGGTTGTAGTGAG[C/T]CGAGATTGCGCCATT	114804
rs374725944	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161641	ATCTGAAGCAGTGCC[C/T]GGAAGGCTGTGAAGG	114804
rs374770769	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76218558	GCTAAGGTGGGAGGA[C/T]TGCTGGAGGTCAAGG	114804
rs374778973	snp	C/T	1.67778e-05	0.00289631	intron-variant	RNF157	GRCh38.p7	17:76161801	AAATGTCCTCTTGTC[C/T]CCTCTCCCACCCACC	114804
rs374862375	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76185117	AGGTCTTGACTCATT[C/G]TTTGAGAATACTGAG	114804
rs374864217	snp	A/G			utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142889	TAGTGCAGCAGGAAG[A/G]AGCCCTGGGTCTCCA	114804
rs374874373	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76185969	ATAGGCATTTAAAAA[C/T]ATAAAACATATATAT	114804
rs374875110	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76192250	CATGGCATCAAACAA[C/T]GAAGCAAAAGTTCAA	114804
rs374885037	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76224408	TTCTTCTACAATTCT[A/G]TGGGAATCTATAGGC	114804
rs374951119	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76187362	CTAATTTTTTGTATT[C/T]TGAGTAGAGATGGGG	114804
rs374970571	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76228551	TGGCTTCTTACTTAC[C/G]TCATCCTACAAGCAT	114804
rs374973150	snp	A/G	0	0	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212667	AGGAGTTCGAGACCA[A/G]CCTGGCCAACATGGC	114804
rs374983948	snp	C/T	0.000153988	0.00877328	intron-variant	RNF157	GRCh38.p7	17:76155216	GCACTCCTCTGGTTG[C/T]GGGAAGGGGGCACCA	114804
rs375017301	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76216470	ATCAAGAATAGTCTG[C/G]GTGTGGTGGCTCACA	114804
rs375045427	snp	C/T	0.00755907	0.0610114	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146841	ACTGTAGAGTGTGGC[C/T]GTGAGGTTGAGAGAG	114804
rs375048741	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76201305	AGCCTTGGCAACATA[A/G]TGAGACCCTAGTCTC	114804
rs375062059	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76190237	AGTGGCACAATTTCG[A/C]CTCACTGCGACTTCC	114804
rs375063653	snp	C/T	6.59055e-05	0.00574007	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161588	TGGGGTTAAAGCTGG[C/T]TGGGGACAAGGGGCC	114804
rs375176278	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76235101	TTAAAATAGGGTAGC[A/G]ATAGTCCTCCAACTT	114804
rs375284394	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76175085	CATCCGTCCGTCTAT[C/T]CATCCATCCTGTCCA	114804
rs375293863	in-del	-/CCCCC			intron-variant	RNF157	GRCh38.p7	17:76181510	CACTGCCAGCAGCCA[-/CCCCC]CAGCCACAATGGATA	114804
rs375336058	snp	C/T	0.00074234	0.0192515	intron-variant	RNF157	GRCh38.p7	17:76155540	ACAGAGAAGCCAGGG[C/T]GGTTCCCGTCCCTTC	114804
rs375395766	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76174157	GCTTTTCCATCTGAC[C/T]TCAGACGACAGGGAA	114804
rs375406048	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76165342	GCCCAGGCTGGAGTG[C/T]GGTGGTGCCATCTCA	114804
rs375408613	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76185531	CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTCACT	114804
rs375411739	snp	A/C/G/T	0.000116998	0.00764776	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76155667	AGACATGGAGGAGAC[A/C/G/T]GTGTCAGTGCTGATC	114804
rs375445064	snp	A/C/G	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241849	CCTGACCTCCGCCCC[A/C/G]CAAAGCGCTGGGATT	114804
rs375463647	snp	A/G	0.0134861	0.0810011	intron-variant	RNF157	GRCh38.p7	17:76210507	AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCA	114804
rs375470131	snp	C/T	4.52776e-05	0.00475781	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76173757	TTCTCAGAGTCTTCA[C/T]GGGTTCTTGGGGAGG	114804
rs375473189	snp	C/T	0.000116189	0.0076211	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152516	CTGTGTTTTTCTCTG[C/T]GTTGCTGTCCTTAAA	114804
rs375474263	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76210393	GGTCAGATCGAGACC[A/G]TCCTGGCTAACACAG	114804
rs375479163	snp	C/T	0.000153988	0.00877328	intron-variant	RNF157	GRCh38.p7	17:76162673	GTCTCTACTGAGAGA[C/T]AAGAGTGGGAACTCC	114804
rs375535776	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76193573	ACACATACAAGTTTC[C/T]ACCATAGTGACTGAA	114804
rs375578489	in-del	-/CCT			intron-variant	RNF157	GRCh38.p7	17:76173906	GGAAGGCACAACTCT[-/CCT]AATTAAGTGAGGAAA	114804
rs375611401	snp	A/G	3.33233e-05	0.00408173	intron-variant	RNF157	GRCh38.p7	17:76158538	GCAGCTATATCCAAC[A/G]TCCATTTAAAGAACA	114804
rs375612725	snp	A/G	0.00318978	0.0398085	intron-variant	RNF157	GRCh38.p7	17:76190652	CGGCCGGGCGTGATG[A/G]CTCACGCCTGTAATC	114804
rs375630195	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76229759	GAGTGGCACACTAAG[C/G]GTACGTATGGGTGCT	114804
rs375666444	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76221963	TATATGAAATATCCA[A/G]ATAGGTAAATCCACA	114804
rs375688422	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167709	TGGTGATGGCTACCC[A/G]AGCATCTGTGTCAAA	114804
rs375702438	snp	C/T	6.60273e-05	0.00574537	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76158411	TCCGAGATGCTGAAC[C/T]GACGGTCTCTGAGAG	114804
rs375842500	snp	G/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76205269	TCAACCACCCAAGTA[G/T]CTAGGAATATAGGTG	114804
rs375914656	snp	C/G/T	4.99167e-05	0.00499562	missense, upstream-variant-2KB, nc-transcript-variant	RNF157	GRCh38.p7	17:76212476	AAGTGGCTGGCAAAA[C/G/T]AGCTTCCTAGAGAGG	114804
rs375935640	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76157212	ACCTCGTGATCCGCC[C/T]GCCTCGGCCTCCCAA	114804
rs375939606	snp	C/T	0.000153988	0.00877328	stop-gained, intron-variant, utr-variant-3-prime, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145254	ACAGCCAAAGGGCCC[C/T]ACACACAGGGCCTCG	114804
rs375990943	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76170957	AAGTGCAGTGGCACA[A/G]TCTCGCCTCACTGCA	114804
rs376023152	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76181776	AGCTGGGTGTGGTGG[C/T]GTGTGCCTGTACTCC	114804
rs376032465	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76178349	GTCCAGCCACAGCCT[C/T]GCAGACAGCTGGCAC	114804
rs376066874	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213913	TAACATGCCCAGAGA[C/T]GGCATAGAAGCTCTG	114804
rs376074377	snp	C/G	0.000153988	0.00877328	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152500	GTTAGAGAGGGGCTG[C/G]CTGTGTTTTTCTCTG	114804
rs376148517	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76166220	CCTCAGGTGATCCAC[A/C]CACCTCGGCCTCCCA	114804
rs376171219	snp	A/G	0.00199481	0.0315187	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146639	CCAGTGTGCTCCTAA[A/G]TGCTCCCTGCAGCCT	114804
rs376171403	snp	C/T	0.000142122	0.00842857	missense, intron-variant, utr-variant-3-prime, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145305	CTGGATGACAAGCGC[C/T]GGCGCTGGGCATTCC	114804
rs376187556	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155579	CTCCTTCTTCTGAGG[A/G]GGCCCTGCTGGCAGG	114804
rs376201609	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76201464	TTACAGTGAGCTATG[A/G]TTGCACCACTGCACT	114804
rs376215290	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76163525	AACCCCAACTACCAA[G/T]GCCCAATCCCACTCC	114804
rs376234733	snp	C/T	6.61408e-05	0.00575031	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76167096	GTACTGCACAGTCTC[C/T]GACTGGAGGCTGTTG	114804
rs376297487	snp	A/G	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76157202	CGATCTCCTGACCTC[A/G]TGATCCGCCCGCCTC	114804
rs376301198	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76177101	AACAGGCAGAGCTCA[C/T]GGCGATGTCACCCTG	114804
rs376332243	snp	C/T	8.24314e-05	0.00641942	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161878	TTGTTGGCCTGGTAG[C/T]GCAGCGTGTCTGCAC	114804
rs376370958	snp	A/G	0.000807317	0.020075	intron-variant	RNF157	GRCh38.p7	17:76162674	TCTCTACTGAGAGAC[A/G]AGAGTGGGAACTCCC	114804
rs376387213	snp	A/G	0.000223297	0.010564	intron-variant	RNF157	GRCh38.p7	17:76166973	CCCTAGGCCCTTCTG[A/G]GTGGATGTGGGAAAC	114804
rs376394643	in-del	-/CCCC			intron-variant	RNF157	GRCh38.p7	17:76212354	GGAGTAAACTGATTA[-/CCCC]CAGCCATACCACAAC	114804
rs376400360	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76200817	AGCAGGCCACTTCCA[C/T]ACTGAATCTCATACC	114804
rs376457438	snp	G/T	0.000153988	0.00877328	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76158489	CAGCACGGAAGAGTT[G/T]TGGGAAGTGGATCTG	114804
rs376460181	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76218092	TTTTTGCCACAATAA[C/T]AAACACATAAATATC	114804
rs376476911	snp	A/G	0.00438332	0.0466095	intron-variant	RNF157	GRCh38.p7	17:76183233	TGAGCCACCACGCCC[A/G]GCCTCACGTGGGAAT	114804
rs376479885	in-del	-/T			intron-variant, upstream-variant-2KB, downstream-variant-500B	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142067	TTAATTTCACCAACC[-/T]TTTAAGTCACAGGGA	114804
rs376484295	snp	C/T	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76203187	GTAGAGACAGGGTTT[C/T]GCCATGTTGGCCAGG	114804
rs376484532	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76235388	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT	114804
rs376572665	snp	A/G			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213169	AAGTAGTTATTCCAT[A/G]TATTGAAGAATCTCA	114804
rs376594896	snp	C/T	0.000307953	0.0124049	intron-variant	RNF157	GRCh38.p7	17:76155550	CAGGGCGGTTCCCGT[C/T]CCTTCCCTTACCTCT	114804
rs376603206	snp	A/G	1.68156e-05	0.00289957	intron-variant	RNF157	GRCh38.p7	17:76167003	CCCTCCCCAGAGGCA[A/G]CTCACCTCCTCTTCG	114804
rs376603824	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76162495	CTGGACGCTGGCTTA[C/T]GATTTCTCACTTGGC	114804
rs376609806	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76235323	CTGCCTCAGCCTCCC[A/G]AGTAGTTGGGACTAC	114804
rs376647382	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76176025	GCACAAGACAACAAC[A/G]GCAAATCTGTTCAGG	114804
rs376647801	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76194822	AGATCGAGACCATCC[C/T]GGCTAACATGGTGAA	114804
rs376723711	snp	A/T			intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153453	AGCAATAGGATGACA[A/T]CTGCTGGTGCGTCTG	114804
rs376743828	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76190818	GAGGCTGAGACAGAA[G/T]AATGGCACGAACCCG	114804
rs376824849	snp	G/T			intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76148765	CTGTAGAGATGGGGT[G/T]TCACTGCATTGCCCA	114804
rs376844326	snp	G/T	1.64776e-05	0.00287028	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154355	GGAAGGCCCTGTGAG[G/T]CTATGAAGCGGCAAA	114804
rs376861594	snp	C/T			upstream-variant-2KB	RNF157	GRCh38.p7	17:76240841	TCCCGGCTCGGATTA[C/T]CGCGCAGGGAGCCGC	114804
rs376945608	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76203745	GCATGACCCACCACG[A/C]CTGGCCTGTAAAAAG	114804
rs376954375	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76168701	GAAGCTCATGTTTCC[G/T]GCACCTCAAGTCTTC	114804
rs376962117	snp	G/T	1.65729e-05	0.00287857	intron-variant	RNF157	GRCh38.p7	17:76159317	CGGGGGCAACAGTGT[G/T]GAGCACTGGCTACTC	114804
rs376965298	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76172926	TAACATTGATGATGA[C/G]GATTAAGCAACCAAC	114804
rs376972210	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76217005	AAATTACAAAGTTGG[A/C]AAAATTGTTCTTACT	114804
rs376988448	in-del	-/GAG			intron-variant	RNF157	GRCh38.p7	17:76173811	TCAGAAACAAAGCAG[-/GAG]AAGGTGGTGTGTTTA	114804
rs377005777	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76211401	CCCACTCTCAATTCC[C/T]ACCACATTCAATCAC	114804
rs377143342	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76198441	AAGTTCAAAAGGCTT[C/T]GTGTCTACTCCACGA	114804
rs377182641	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157	GRCh38.p7	17:76156100	GCCTACTTGTCATGC[A/T]GTACAGGTATTAGCT	114804
rs377193605	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76166082	CAGGTTCAAACGATT[C/T]TGCTGCCTCAGCCTC	114804
rs377195585	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76219833	TACAGTAATCATATT[A/G]TTGGTGACAGTATTT	114804
rs377198660	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76185643	CCCGGCTAATTTTTT[A/G]TATTTTCAGTAGAGA	114804
rs377238896	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76201056	ACTCCCTTAATTTTC[C/T]TACTTCTAAATATTC	114804
rs377253210	snp	C/T			missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76162002	CTTCGTCTTCAGCCA[C/T]CTGGCCAAGGAGAAA	114804
rs377265029	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76235261	GGAGTGCAGTGGCAC[A/G]ATCTCGGCTCACTGC	114804
rs377281981	snp	G/T	0.000310457	0.0124552	intron-variant	RNF157	GRCh38.p7	17:76162048	GCACAAAGCCCTTCC[G/T]GTCCCATACTTTACT	114804
rs377288876	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76162127	AAATCTGCATTGACA[C/T]TGGACTTTGTCATTT	114804
rs377309826	snp	A/G	1.64844e-05	0.00287087	intron-variant	RNF157	GRCh38.p7	17:76212340	CTTAAGCTCCAAGTA[A/G]GAGTAAACTGATTAC	114804
rs377318435	snp	C/T	5.03056e-05	0.005015	intron-variant	RNF157	GRCh38.p7	17:76162645	AGCAAACAGAAAGGT[C/T]CAAGGACAGGCTGTC	114804
rs377352432	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76223739	ACGTACAGCCTCCCT[C/G]TTCAGAATAAAATAT	114804
rs377384433	snp	A/G			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76214333	TGTGCTGCTTGTGTT[A/G]TGAGTGTATAGGAGA	114804
rs377428649	snp	C/T	1.74366e-05	0.00295263	intron-variant	RNF157	GRCh38.p7	17:76162542	ATTCAGAATTTTGGG[C/T]AAAACTTACCTTAGA	114804
rs377439729	snp	C/T	0.188	0.24219	intron-variant	RNF157	GRCh38.p7	17:76210477	TGCCTGTAGTCCCAG[C/T]TACTCAGGAGGCTGA	114804
rs377453550	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76173138	AAAAATACAAAAAAT[C/T]AGCCGGACGTGGTGG	114804
rs377485146	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76220698	GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAACA	114804
rs377506416	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76194042	AATCACCTCTTTCCA[A/C]GGCACATTCTGTTTT	114804
rs377525096	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76225497	GTCCAGGTCTTCCTG[C/T]TCTATTATTTTTTTT	114804
rs377556118	snp	C/T	0.000100002	0.00707042	intron-variant	RNF157	GRCh38.p7	17:76155340	AGAGCACAGTTTTTA[C/T]AGGCTCTTCCATAAA	114804
rs377578045	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76230730	GCAATCCCAGCTACT[C/T]GGGAGGCTGGGGCAG	114804
rs377581288	in-del	-/AT/ATAT	0.131381	0.220067	intron-variant	RNF157	GRCh38.p7	17:76182760	TTCAGGCCTCGTCTC[-/AT/ATAT]ATATATATATATATA	114804
rs377585028	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76223130	CTCCTGACCTCGTGA[C/T]CCGCCCACCTGGGCC	114804
rs377594763	snp	A/G	5.00404e-05	0.00500177	intron-variant	RNF157	GRCh38.p7	17:76159580	CTCTGAGGACTAGGG[A/G]AATCAGAGACAGGTT	114804
rs377626023	in-del	-/GA			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150626	CACAGCTAAGAAAGA[-/GA]CATCATCTTCACCCA	114804
rs377678768	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76168989	TGAAAGCTTACAGAC[A/G]GTCCTCTTTCTCAGC	114804
rs377693807	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76159844	AAAGTAAGGAAAAAA[A/T]ATCACCAGTAATCAA	114804
rs377700885	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76235348	GACTACAGGCTTCTG[C/T]CACCATGCCTGGCTA	114804
rs377715203	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76173933	AGGAAACTGAAACTC[C/T]GACATACTGAGTCAA	114804
rs377719776	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155618	AAGAGAGAGCCTCTC[C/T]CTCCTCTTCAGTGCC	114804
rs386386668	in-del	-/TT			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76148281	TTTTTTTTTTTTTTT[-/TT]TGAGACAGGGTCTCT	114804
rs386386670	in-del	-/TT			intron-variant	RNF157	GRCh38.p7	17:76168440	CTATTTTTTTTTTTT[-/TT]TCTTCCAGTTGCGTA	114804
rs386799291	in-del	AG/C			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153123	CCCTCTTTTTTTCTC[AG/C]TGAAACAGAGAGAAG	114804
rs386799293	multinucleotide-polymorphism	ACG/GCA			intron-variant	RNF157	GRCh38.p7	17:76166914	AAGCATGGCCTTCAA[ACG/GCA]TCCGAGCAGCCCCTT	114804
rs386799294	multinucleotide-polymorphism	CA/TG			intron-variant	RNF157	GRCh38.p7	17:76198278	GAGAGCCTGTTGATA[CA/TG]GGGACATTCTCTTAT	114804
rs386799295	multinucleotide-polymorphism	CAG/TGA			intron-variant	RNF157	GRCh38.p7	17:76198278	GAGAGCCTGTTGATA[CAG/TGA]GGACATTCTCTTATG	114804
rs386799296	multinucleotide-polymorphism	CAGG/TGGC			intron-variant	RNF157	GRCh38.p7	17:76198278	GAGAGCCTGTTGATA[CAGG/TGGC]GACATTCTCTTATGA	114804
rs386799297	in-del	GCAA/TT			intron-variant	RNF157	GRCh38.p7	17:76207227	TTGAGATCAGCCTGG[GCAA/TT]TAAAGCAAGAAAGAC	114804
rs386799298	multinucleotide-polymorphism	CA/TG			intron-variant	RNF157	GRCh38.p7	17:76210321	AGAACCCGCCGGGCG[CA/TG]GTGGCTCATGCCTGT	114804
rs386799299	multinucleotide-polymorphism	CT/GC			intron-variant	RNF157	GRCh38.p7	17:76210326	CCGCCGGGCGCAGTG[CT/GC]TCATGCCTGTAATCC	114804
rs386799300	in-del	CAATAGCAAC/GGTGTAGAACAGTCTA			intron-variant	RNF157	GRCh38.p7	17:76236868	AAGCAAACAGAGCAA[CAATAGCAAC/GGTGTAGAACAGTCTA]ATAGCATGCTATGCT	114804
rs397688217	in-del	-/TT	0	0	intron-variant	RNF157	GRCh38.p7	17:76163210	TTTTTTTTTTTTTTT[-/TT]GAGATAGGGTCTTGC	114804
rs397735476	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76224731	TTTAAAAAAAAAAAA[-/A]GAAAGAAACTGCAAA	114804
rs397857460	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76220388	TCGTAATGATATCTA[-/A]AAAAAAAAAAAAAAA	114804
rs398031640	in-del	-/A	0	0	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76148582	GTGAGACTCCATCTT[-/A]AAAAAAAAAAAAAAA	114804
rs398041912	in-del	-/T	0.5	0	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150147	CACACATATTTTTTT[-/T]CTTGGAAAATCTTAG	114804
rs398041913	in-del	-/A	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76175854	AAGAAAGAAAAAAAA[-/A]TCCTGGCACTCTTTA	114804
rs398041915	in-del	-/T	0.5	0	intron-variant	RNF157	GRCh38.p7	17:76192859	TTTTTTTTTTTTTTT[-/T]GAGACAGCATCCGCT	114804
rs527240790	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76163068	AAAAAGATGGGAAGG[A/G]AAAATATGGATGCAA	114804
rs527241382	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157	GRCh38.p7	17:76156468	CAGAGGCCGCAGCTT[C/T]TCTCTTCCGTCCTCA	114804
rs527323262	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76201100	TCCTTCCTCTACTTA[G/T]AAGTATTTCCACCTC	114804
rs527368535	snp	C/T	0.00398564	0.0444627	intron-variant	RNF157	GRCh38.p7	17:76194826	CGAGACCATCCTGGC[C/T]AACATGGTGAAACCC	114804
rs527375589	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76156946	TTTGTCTTAGTTCAC[A/G]CAGTCCTTCTTTTTT	114804
rs527389929	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76194931	GAGGCAGCAGAATGG[C/T]GTGAACCCGGGAGGT	114804
rs527413119	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76157218	TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCC	114804
rs527435917	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76235587	ACATTAAAACTTTTA[C/T]AGTTATTCGACAAAG	114804
rs527439636	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76228890	GACTGCGCCATTGGA[C/T]TCCAGCCTGGGCGAC	114804
rs527451957	snp	A/G	0.00318978	0.0398085	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76152058	ACTGGGCCACCTGAC[A/G]TGGTACCTGCAAGGC	114804
rs527465637	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144599	GGCGTGAGCCACCGC[A/G]CCCGGCCAAGAGCTC	114804
rs527525149	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76189698	TTTCCATCCCCATGG[A/C]TGAGGAAACAAAAGG	114804
rs527532735	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76189370	AATGCAGAGATGAAA[C/T]GGAAGGAGCTCAGGA	114804
rs527534210	in-del	-/CTGGCCCCGGCC	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76177126	ACCCTGCCCTGGACA[-/CTGGCCCCGGCC]CTGGCCCCGGCCCAG	114804
rs527553111	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76198795	ACAAAAATTCGAAGC[C/T]CACAGGGAGGCATAC	114804
rs527579785	snp	A/G	0.00279162	0.0372561	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147196	TAAGGCAATATTAAT[A/G]TTGCCTTTAAAGTGA	114804
rs527606159	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76182893	AATAATATGAAAACT[A/G]TATTATTACCATCAA	114804
rs527606750	snp	C/T	0.00795532	0.062565	intron-variant	RNF157	GRCh38.p7	17:76167989	ACTTCTGGTATCTCA[C/T]AGTGCTACCACTACA	114804
rs527639838	snp	A/C			upstream-variant-2KB	RNF157	GRCh38.p7	17:76242123	CCAGGGCTTTCAGTC[A/C]TCCCTGTGGGAGGGA	114804
rs527640704	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76233580	TCTCAATCTGTCACC[C/T]AGGCTGAAGCGCAGT	114804
rs527657615	snp	C/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149635	AACAGTGGAAGCAGA[C/G]ACACATTCTGCCTAG	114804
rs527672413	in-del	-/TAAATAAATAAATAA	0.029753	0.119687	intron-variant	RNF157	GRCh38.p7	17:76205730	TCCATCTCTAAATAA[-/TAAATAAATAAATAA]ATAAATAAATAAATA	114804
rs527694149	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150020	GCTGGGCGACAGAGC[A/G]AGACTCTGTCTCAAA	114804
rs527704385	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76227401	GCTGGGATTACAGGC[A/G]TGAGTCACTGCGCCT	114804
rs527758878	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76186631	ATATGCTCTGAGGTC[C/T]ACTAGGCTAGAAATC	114804
rs527762984	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76180463	CTGCAATTACAGCTT[A/G]GCAAATCATGAAAAA	114804
rs527764830	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76187961	CTAATGGAAAAATCT[A/G]TTCTGCAGCTAGTTT	114804
rs527801723	snp	C/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76181256	ATGGCAAACAGTACT[C/G]AATTCTGTGAAGGTT	114804
rs527812601	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76227839	CCAAGATCGCCCCAT[C/T]GCACTCCAGCCTGGG	114804
rs527814887	snp	A/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76220665	TTATTATTTTTTTTT[A/T]TTTAGTTAGCTGGGC	114804
rs527831830	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76143621	GGACGACAGGCCCCC[C/G]TCTCCATCAGGGCAG	114804
rs527840805	snp	C/T	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76175274	GGTTTTACTTTTTTT[C/T]GCAGCTATAAATGTT	114804
rs527872792	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76221545	AAATCCAAAGTACAG[A/T]CTTTATTTTATTAAA	114804
rs527944472	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76214000	CCTTGATAATAAACT[C/T]GTAAATGTGTTTCTC	114804
rs528006439	snp	A/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76169716	TCCCAAGTAGCTGGG[A/T]TTATAGGCGTGTGCC	114804
rs528024254	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76162465	ACTGATTTCAGAGTT[C/T]GGCACGCTAAATTTC	114804
rs528027739	snp	A/G	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76238063	CATTCCAGCCTGGGC[A/G]TGACAGAGAGAGACG	114804
rs528069308	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146403	CTCGCCTCTCCCCTG[A/G]GAGTCCTCTTCATCT	114804
rs528091488	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76225089	AGGCAGAAGAATCGC[C/T]TGAACCTGGGAGGCA	114804
rs528120889	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76226801	CAGGAAGCTCATTTC[G/T]GTCATGTTGCGGTGC	114804
rs528123071	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76191705	CTTGAGCCTGGGAGG[C/T]TGAAACTACAATGAG	114804
rs528124713	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76184084	TAATCCTAGCTACTT[A/G]GGAGGCTGAGGCAAG	114804
rs528156177	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76177961	AGGACACCCTGGCTG[C/T]GGAAAGAGCTACCCA	114804
rs528180012	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76202333	TGGGGTAAGTGGTGG[A/C]CTCTCACAGAGGCTG	114804
rs528191608	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76178417	AGCTGGCGTGTCTGA[C/T]TGCACAGTGGCCGGA	114804
rs528280814	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76218301	AACATTCTAAGGTAG[C/T]CAAAGAAAGAAAAGC	114804
rs528281978	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76217700	TTACCAGGAGAAACA[C/T]GTCACTCACAGATAA	114804
rs528326664	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76204738	GTACTAGAGAAAGAA[A/G]AAAAGTACACTGTAT	114804
rs528369062	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76173115	CATGGTGAAACCCCG[C/T]CTCTATTAAAAATAC	114804
rs528435273	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76170537	GGGAGAGTCATCTGC[C/T]TGCCTTTGGCCAAGG	114804
rs528444960	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76177147	CCGGCCCTGGCCCCG[A/G]CCCAGTGAGGACCTG	114804
rs528499501	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76209393	ATTTACTTCAAGCTT[A/G]TCCAACCTGCGGCCC	114804
rs528559068	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76164004	AACAGTGTAGAATTT[A/C]AGGTATCTATCACCC	114804
rs528562986	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76209916	AGGCTCACACCACCA[C/T]GCCCAGCTAATTTTT	114804
rs528583287	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76171161	CCTCCCAAAGTGCTG[A/G]GATTACAGGCATGAG	114804
rs528594250	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76164891	ACAGTCGCCCTCCCT[A/G]ATCTGCAGTTTCATT	114804
rs528632312	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76157799	AGAAGCTGCATAAAC[C/T]TTTGTTAAGTGAGGT	114804
rs528632346	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76165726	TCTGTTGCCTGGGCT[A/G]GAGTGCGGTGGCATG	114804
rs528639783	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76218218	AAAAGTCAAAATTCT[A/G]GAGGGGAAGAAAATC	114804
rs528668650	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76158339	TGAGGCATGCAGGTA[A/G]GAGGGAAGTCCCTGG	114804
rs528693728	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76202841	CACCATGTTTATTTG[C/T]AATGCTGTTAATCCT	114804
rs528712711	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76195974	AATGACCCAATGACC[C/G]GGAAGGTACTATCCT	114804
rs528789388	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76190931	AAAAAAGTTTACACG[A/G]CTGAATGCAGTGGCT	114804
rs528798576	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76221026	TTCAGGAGGCTGAGG[C/T]GGGAGAATTACTTGA	114804
rs528840669	snp	C/T	3.29473e-05	0.00405864	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167718	CTACCCGAGCATCTG[C/T]GTCAAAGGTGAACTC	114804
rs528841213	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76237665	GAGACCCTGGCCATA[C/T]CAATTCATTTCTCTG	114804
rs528855469	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76174209	TTCGGTGAGGCCATG[A/C]GGTATCCCAGGAGTT	114804
rs528877387	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76220521	TACCTCTGGGTGAGT[C/G]AATAATTAATAGATG	114804
rs528887149	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76211998	ACTTACGTTCTAGAG[A/G]AGGAGGCAGACAATA	114804
rs528975500	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76168338	TTATAATAGTCCAGT[A/G]CATTTGTGTCTGTAT	114804
rs529013188	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76161457	CTTGCTGCAATGCCA[C/T]GTAGAGAAGCATGAA	114804
rs529020860	snp	A/G	0.000189627	0.00973539	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76155676	GGAGACGGTGTCAGT[A/G]CTGATCTGGGAGGAT	114804
rs529035009	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76190123	TGACCCACTGATACT[A/T]ATTACCCTTACTTCT	114804
rs529057474	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76162207	CTAAAATTGAGAGGA[C/T]GAGACTAACCACTCG	114804
rs529059568	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241003	GCCGGCGGAGGTCTT[C/T]GGAAATCTCATGCAG	114804
rs529094135	snp	C/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76207836	CAGTAATGGCAAAAC[C/G]CAGAGGTCAGCTCAG	114804
rs529094187	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76199544	TAGATGTGAGCCACT[A/G]TGCCCTGCCAAAAGC	114804
rs529133293	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76237704	TTTTCTTATCAGTGA[A/T]ATGAATGGGAGGCCA	114804
rs529134391	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76200199	GTGAGCCAAGATCGC[A/G]CCACTCCATGCCAGC	114804
rs529162830	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241622	TTTTTGTTTTTCTGT[C/G]TTTTGAGACGGAGTC	114804
rs529191468	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150096	CCTTGCCACAGAAGC[A/G]TTCCCATTTTTACTG	114804
rs529223001	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76234338	CTATTATGAGTAATT[C/T]ATGTGCAAGTTTTTA	114804
rs529275492	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76159629	TTTTTGTTTTATGAC[A/G]TGATCATGCTACTTC	114804
rs529307627	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76233069	GTGACTACAGGTACC[A/G]GCCACCACGCCCAGC	114804
rs529310539	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154629	TAAGGTGGAAGTAAA[A/G]ATTACTAAATGAAAG	114804
rs529319693	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76198790	ACAGGACAAAAATTC[A/G]AAGCTCACAGGGAGG	114804
rs529358034	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76192709	AAGCTTGACTAGCAG[C/G]TGAAACCCTCTGGTT	114804
rs529375531	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76193224	TGTCTATCTCATAGG[A/G]TCATTAAGATCAAAT	114804
rs529392378	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76232310	GGAGGAGTGCCTGAG[A/C]CCAGTAGGTCGACGC	114804
rs529415427	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76239763	GGACCCCGCGAGGCA[A/G]GTAGGCTTTGGGCCG	114804
rs529432703	snp	G/T	0.000798403	0.0199641	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147939	AGGTAGATTTTGGGA[G/T]TACATTCAGGAAAAT	114804
rs529450724	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76155019	TCCCTCTTGAACTCA[C/T]TCCACACCAGTGACC	114804
rs529466048	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76226889	GCTGCTGCTGAATGC[C/T]GTGGGAAGCGCCATG	114804
rs529521731	snp	C/T			utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144321	CAGATTCAAGGGCTC[C/T]TTCTTTTTTTTTTTT	114804
rs529577188	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76227294	CTCAGCTAATTTTTG[C/T]ATTTTTAGTAGAGAC	114804
rs529634645	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76201896	CTACAAGTAATGCTA[C/T]AATATACATTGTAAA	114804
rs529639533	snp	G/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76180274	AAAACAGGCCTCAGA[G/T]CAAGACTCATGAACA	114804
rs529671436	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76194954	CGGGAGGTGGAGTTT[A/G]CAGTGAGCCGAGATA	114804
rs529717170	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76152093	ATGTGGGGTGGAGAG[G/T]GGTTAGGCCAAATCG	114804
rs529719362	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76218590	AGGAGTGAGCTATGA[C/T]CACACCCCTGGACTC	114804
rs529721485	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76189427	GCTCCTGTGCTGCTG[A/G]TTACGGTGACTTTAG	114804
rs529789703	snp	A/C/G	0.00199529	0.0315338	intron-variant	RNF157	GRCh38.p7	17:76229667	GGCACTTTATCTGAA[A/C/G]AGCTGGCACCAGAAC	114804
rs529791313	snp	A/G	0.000207533	0.0101845	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145221	GAGGGGAGCCCAAGT[A/G]CAGAGGCTGGGGCTC	114804
rs529804750	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76190150	TTCTGTTAAGTGCTC[A/C]GGCTAACTGCTTGCT	114804
rs529807399	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76233651	AAGCAATCCTTCTGC[C/T]TCAACCTGCCGAGTA	114804
rs529857167	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152602	CAATAATTAAGCGGA[C/T]AAAGAGTGGACAAGA	114804
rs529859054	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76223967	TGGCCAGAGCAGCTC[C/T]AGACACTACTCCTTA	114804
rs529870887	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76164924	CCATGGTTTCAATTA[C/T]CCGCCATCAACCACT	114804
rs529879125	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145499	GCGAGCCACAGCACT[C/T]GTGTGTGAGAACGGA	114804
rs529946752	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76182961	GTTGGTTACTTTTCG[C/T]TCTTGTTGCCCTGGC	114804
rs529973488	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76203220	GGTCTCAAACTCCTG[C/G]CCTCAAGCAATCCAC	114804
rs530000649	snp	A/G	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76177249	ACAGGCAGCAGCCCC[A/G]CCTTGGGCTGTGGAT	114804
rs530023846	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76143781	TTTTTTTTTGTTTGA[C/G]ACAGAGTTTCGATCT	114804
rs530039849	snp	A/C	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76177749	AGCAGAGGTTGGGAC[A/C]ACCAGCTGCAGAGAG	114804
rs530136817	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76221645	GTTCATGCTCCTTCA[C/T]TGGTTCTTCTAAAAT	114804
rs530138761	snp	A/C	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76228582	ATACTGGTCTCCCCA[A/C]CTCAAATAACAAATA	114804
rs530152850	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76215618	CAGAGAAGAAAATTC[C/T]AGCAAAAACTGAACC	114804
rs530154757	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76188378	CTTATTCTCAGCAAC[C/T]TCTTCTCTGTGGTTC	114804
rs530158032	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76176009	GTACACACACATACA[C/T]GCACAAGACAACAAC	114804
rs530194481	snp	G/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76169849	CCTTCCCAAAGTGCT[G/T]GGATTATAGGCGTGA	114804
rs530310870	snp	C/G			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212641	CTGAGGCAGACAGAT[C/G]GCCTGAGATAAGGAG	114804
rs530326277	snp	C/G	0.00398564	0.0444627	intron-variant	RNF157	GRCh38.p7	17:76163144	CACACCATGAAGCCA[C/G]CCCATCCCCAACATG	114804
rs530388438	snp	C/T	0	0	intron-variant	RNF157	GRCh38.p7	17:76209034	TTAATGATTACTACA[C/T]AAAAGCAACAACAAA	114804
rs530421360	snp	C/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76170294	GTGCAGTGCTGTGAT[C/G]GTGACTCATTGCAGC	114804
rs530460026	snp	C/T	0.00636936	0.0560724	intron-variant	RNF157	GRCh38.p7	17:76163680	TTATATCCCACTCTC[C/T]GTTTTAACAGTCTGT	114804
rs530464807	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76185618	GGGACTACAGGCACC[C/T]GCTACCACGCCCGGC	114804
rs530471083	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76205719	ACGGAGCAAGACTCC[A/G]TCTCTAAATAAATAA	114804
rs530479467	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76225882	CCAGCTCTTTGCACT[C/T]GCCAGTGAGAGCCTC	114804
rs530487312	snp	A/T	0.00318978	0.0398085	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149394	TAGACTCAAGCAGAG[A/T]CCAGGCGCATGTGCA	114804
rs530495444	snp	C/T	0.00478085	0.0486577	intron-variant	RNF157	GRCh38.p7	17:76237281	GCTGGACACTGTGAC[C/T]GTCATTACAAGGACA	114804
rs530531318	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76178350	TCCAGCCACAGCCTC[A/G]CAGACAGCTGGCACC	114804
rs530543549	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76217821	ATTAGTGAGCTATAA[C/T]TTATTAATCAAAACT	114804
rs530543865	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76226291	GGAATGATCTGGAGT[A/G]GAGGACTGGACCCCT	114804
rs530748479	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76205553	AAGATGGTGAAACCC[C/T]GTCTCTACTAAAAAT	114804
rs530750116	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76160540	ATTGATTTTTAATGT[C/G]GTTGAACTTTTTAAA	114804
rs530774037	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76165136	TTCTGTACGATCTGC[A/G]GTTTCAGGCATCCAC	114804
rs530807797	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76210004	ACCTTGTGATCCGCC[C/T]GCCTCGGCCTCCCAG	114804
rs530810905	in-del	-/C			intron-variant	RNF157	GRCh38.p7	17:76231434	TCAACTTTTTACTGT[-/C]TTTTGAGGCCCACCA	114804
rs530820677	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76202745	ATCGAGGCTTCAAAC[A/G]AGTCACAACAATGAT	114804
rs530822523	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76159749	CACACACTGTAGATC[C/T]TGCTTATTGGTAAGC	114804
rs530848799	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76227041	GGGAGGAGGGAAGGC[A/G]TGCACGTGCGGAAAA	114804
rs530864861	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76154757	GGGCTCTCACTGTGA[A/G]CTGGCGTTCCACAGC	114804
rs530996568	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76179549	AATACAAAAATTAGC[C/T]GGGTGTGGTGGCACA	114804
rs531008886	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146531	CTGGCTCCCTGGGGT[A/G]GGGAAGGCATGTCGT	114804
rs531010912	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154006	GCTTAGAGAGCTTCC[A/G]AATCTACTTCAGGTA	114804
rs531012425	in-del	-/T	0.0174175	0.0916809	intron-variant	RNF157	GRCh38.p7	17:76227523	GCTATTTTCTTTTCA[-/T]TTTATAGAAGAGGAA	114804
rs531042812	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76191020	TAGTGGGACTGTTTC[C/T]ACAAAAAGAAAAAAA	114804
rs531073878	snp	A/C			utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144514	GGGTTTCGCCGTGTT[A/C]GCCAGGATGGTCTCG	114804
rs531159525	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76197434	TTGGAAGGCTGAGGC[A/G]GGAAGATCACTTGAG	114804
rs531183463	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76195221	CCTACAAGCGGGGTA[C/G]AGCAAGGCTGGAAAC	114804
rs531203656	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76171529	TATAATTACTTAATG[A/G]GGTTTTCAGAGGAAG	114804
rs531205162	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212949	TTTCCTGATTTGGGA[C/T]AATGGCACAAAATAA	114804
rs531218296	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76207907	CTCCAAGAGAACATA[C/T]CACTGCCACTCGTCT	114804
rs531240290	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76185039	GTAAAGAACACATCA[C/T]AAAATGGCATAGATC	114804
rs531295311	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76162404	CAAAGTGGTAAAAGC[A/G]TAATGATCTGAAATG	114804
rs531322962	snp	C/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149180	GCTAGAATGACAAAA[C/G]TGCCTCTAAGCCCCT	114804
rs531346272	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241733	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGAGACTA	114804
rs531358248	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76242348	TAAACGGGACATCCC[C/T]TCCCTTTGTGGGTTT	114804
rs531371708	snp	C/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149430	TCTGACGGGAGAGAG[C/G]TGGCCACAGGAGCAA	114804
rs531398564	snp	A/G			intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154150	TACCATTAAGAAGAC[A/G]ATCTTTCCTCTAACA	114804
rs531410422	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76170216	GCTCAACATCCAGTA[C/T]GCCAGGATCCACTCA	114804
rs531412404	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76143971	CAGCACACTGCTGCT[C/G]GCCACATGCTGCTGC	114804
rs531450865	snp	C/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76211859	ATTCTCATATCAACT[C/G]ATATATCAAGAGAAA	114804
rs531456396	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76225812	AAATCTTTCAGGTAC[C/T]GGATCTCCTTGGCCA	114804
rs531461910	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76152118	AAATCGTTAAGTTTT[G/T]CTTCTTTCTTCCTAT	114804
rs531507450	snp	C/G	0.00438332	0.0466095	intron-variant	RNF157	GRCh38.p7	17:76181714	AGAGTTTGAGACCAG[C/G]CTGGCCAACATGGTG	114804
rs531536354	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76228782	CAAACTTAGCCGGGC[A/G]TGGTGGTGGGCGCCT	114804
rs531538059	snp	C/G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76148381	ACGCCATTCTACTGT[C/G/T]GCAGCCTCCTGAGTA	114804
rs531562694	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76188089	CAAGATTCTGTAAAC[A/C]AAGTGAACTACTTTC	114804
rs531564392	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76194819	AGGAGATCGAGACCA[C/T]CCTGGCTAACATGGT	114804
rs531588951	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76191698	AGGACTGCTTGAGCC[C/T]GGGAGGTTGAAACTA	114804
rs531599557	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76156997	GATGGAGTCTCGCTC[C/T]GTTGCCCAGCCCAGG	114804
rs531625527	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76193303	TAGTGATCCTTAGTG[A/C]TTAGCATTAGTGATA	114804
rs531645368	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76186203	TCCCATTAAAAAACA[C/T]CGACTCTAAAACTAT	114804
rs531663531	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76193731	TTCTGAAGCCTGATC[C/T]GAAACAATCAGGAGC	114804
rs531714346	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76238084	GAGAGAGACGATGAC[A/T]CAAAAAAAAAAAAAA	114804
rs531728287	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76200013	GAGGCCGAGGCGGGC[G/T]GATCACGAGGTCAGG	114804
rs531738045	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76148724	CACAGGCGTACGCCA[C/G]CAAGCCTGGCTAATT	114804
rs531743557	in-del	-/TTTTTTTCTTTCTTTTT			intron-variant	RNF157	GRCh38.p7	17:76205134	TCCTCTTTTCTTTTC[-/TTTTTTTCTTTCTTTTT]TTTTTTTTGACAGGG	114804
rs531759858	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76233385	AATGTTTTTAATTTC[A/G]AAGAAATCCAATTTA	114804
rs531771699	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76227352	TCTTGAACTCCTGAC[C/T]TCAGGTGATCCGCCC	114804
rs531814228	snp	A/C			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151328	CAGCTTCCCCTGCCA[A/C]AAGCTTGTGTGGGGC	114804
rs531822795	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76240819	GTCGCCCCTCCGCGC[C/T]TGTTTATCCCGGCTC	114804
rs531850206	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76236470	CTTTTAAAGATGCAA[A/G]GATCTTAGAGAAGCA	114804
rs531871965	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, downstream-variant-500B	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142262	CCCCGCCTCTGCCCA[C/G]GAGCTGGAGAGCCGG	114804
rs531918207	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76212192	TCTTCCAGTCCTCTA[C/G]CAACAAGAGATCCCA	114804
rs531918461	snp	G/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76221495	CCAGGTTTCCTCAAA[G/T]AATATATTGTAAGGG	114804
rs531932556	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76222081	AATGTTCTAGAGGCC[A/G]GGCGCAGTGGCGCAC	114804
rs531969242	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76195817	CTCGCACATCAGACT[A/G]AATTGAGCACAAGCT	114804
rs532019232	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76174314	CCCTGCAGCTGATCA[C/T]ATAAAGCAGAGCTCT	114804
rs532042694	snp	A/C	0.00636936	0.0560724	intron-variant	RNF157	GRCh38.p7	17:76190820	GGCTGAGACAGAAGA[A/C]TGGCACGAACCCGGG	114804
rs532056558	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76198669	GGTTACCCTGTATCC[A/G]TTCTCATGACTCTCT	114804
rs532059352	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76168441	CTATTTTTTTTTTTT[C/T]CTTCCAGTTGCGTAG	114804
rs532073620	snp	A/G	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76183078	TAGCTGGGATTACAG[A/G]CGTCTGCCACCATGC	114804
rs532090399	in-del	-/A	0.408139	0.193629	intron-variant	RNF157	GRCh38.p7	17:76224719	TAGCTGATAAGCTTT[-/A]AAAAAAAAAAAAGAA	114804
rs532093691	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76173347	ATTTGATATTCTAAG[A/T]TCAAATTTCCCATTT	114804
rs532155262	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145523	GAACGGAGAGAAGCA[A/G]GTGCTGACAGGTGCA	114804
rs532235468	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76183917	AGTACAGGCTGGGAG[C/T]GGTGGCTCACACCTG	114804
rs532260211	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76230817	TACTCCAGCCTGGGC[A/G]AAAGAACAAGACTCC	114804
rs532296150	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146333	ATGAGAGAATGCGAG[C/T]GTTGGTGAGTATCTG	114804
rs532306273	snp	C/T	0.00557542	0.0525036	intron-variant	RNF157	GRCh38.p7	17:76210319	AGAGAACCCGCCGGG[C/T]GCAGTGGCTCATGCC	114804
rs532322898	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76172528	CCTGGGAGGTGGAGG[C/T]TGCAGTGAGCCGAGA	114804
rs532324712	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76224959	GGCAGATCACTTGAG[A/G]TCAGGAGTTCGAGAC	114804
rs532428323	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76171925	GCCCTTGAATGGTCT[C/T]CATCAAATGTGTGAA	114804
rs532463637	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76165838	TGAGCCACCATGCCC[A/G]GTTACTTTTCTGTAT	114804
rs532474848	in-del	-/A	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76168169	TTTACCCACGTTTCT[-/A]AAAAATATACTTGGG	114804
rs532539843	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76222227	GGCACACGCCTGTGA[C/T]CCCAGCTACTTGGGA	114804
rs532574318	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76222991	CGCCTCCTGGGTTCA[C/T]GCCGTTCTCCTGCCT	114804
rs532582071	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76182327	CATCAGCTTCCTTTT[A/G]CCAGCACATCACATC	114804
rs532597237	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76209194	CCTCAGCCTCCTGAG[C/T]AGCTGGGACCACAGG	114804
rs532599404	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76239962	CCCGGCAGGACGCCC[C/T]TTGGGCTAATTCGCC	114804
rs532609270	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76201958	CTGTAGGAGAGATTC[A/G]GAGAGGTGAAACAGT	114804
rs532617940	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194982	ATAGCACCACTGCAC[C/T]CCAGCCTGGGTGACA	114804
rs532640081	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76165925	TCAGGTGATCTGCCC[A/G]CCTCAGCCTCCCAAA	114804
rs532658007	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76164665	AAACAAAAATAAAAA[A/T]AGAGGGAGAGAGAAG	114804
rs532689051	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76215089	GTGGCAAAAGGCTTG[C/T]TTGTGTATAATACAT	114804
rs532739758	in-del	-/AA			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213570	CAAAACTCCATCTCA[-/AA]AAAAAAAAAAAAAAA	114804
rs532752999	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76209835	AATGATCTTGGCTTA[C/T]TGCAACCTCCGCCTC	114804
rs532779583	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76226861	CGAAGGTGTCTTTGT[C/G]GGTTACAGCAATGCT	114804
rs532793377	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76219757	AGAACTTTAAGAGAC[G/T]GTAATTTAACTGTAC	114804
rs532829653	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76180692	AGCTTCCCAAAGTGC[A/G]GGGATTAGAGGTGTA	114804
rs532844525	snp	A/G	3.34096e-05	0.00408702	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76167018	GCTCACCTCCTCTTC[A/G]GCCCACTCGGAGGGA	114804
rs532902394	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76223040	GGACTACAGGCGCCC[A/G]CCACCATGCCTGGCT	114804
rs532917319	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76160565	TTTAAAAAATTCTAT[A/G]TTGAGTGTGTTTTGT	114804
rs532986125	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76173242	AGTGAGCCGAGATTG[C/T]GCCACTGCACTCCAG	114804
rs533023578	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76211514	GTGAGGAGCACTGGA[A/C]AGATTACTGATCTGT	114804
rs533033904	in-del	-/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76189316	TTTGTGATTCTTCTG[-/T]TAAGAATAAATTATT	114804
rs533086849	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76193796	GCTCCTGGGCAGGCT[C/T]TCCCGCATCCTGCAG	114804
rs533114678	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76231746	CACAAACCCCTCTGT[C/G]CTGTTATTTTTAAGA	114804
rs533160341	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76206197	AGTTGTGCCACTGTA[A/C]CTCAGCTTGGGCAAC	114804
rs533165731	in-del	-/TG	0.00318978	0.0398085	intron-variant	RNF157	GRCh38.p7	17:76182266	TGCTGACGAAGGCTC[-/TG]TGTGTTACGTGAGCA	114804
rs533241361	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76239911	CGCTCCCGTCCTCCC[A/G]TGGAGGGGCTCGGTG	114804
rs533320855	snp	C/T	0.000399281	0.0141238	intron-variant, missense	RNF157, RNF157-AS1	GRCh38.p7	17:76147291	TCAATGTTTATGGGG[C/T]AGGACTCCGGAGCTG	114804
rs533350834	snp	A/G	0.0707826	0.174302	intron-variant	RNF157	GRCh38.p7	17:76198280	GAGCCTGTTGATACA[A/G]GGACATTCTCTTATG	114804
rs533374424	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144652	GAGGCCCAGAAGACT[C/G]GCTCTGCCACCAGAA	114804
rs533401594	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76204618	ACTCTATGTTACAAA[G/T]GGATATACTACCAAG	114804
rs533432452	snp	C/G			utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76143755	CTGCCTTGGAAACAG[C/G]CTTGAATTTTTTTTT	114804
rs533439592	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76197593	AATTTATTTGAGATA[A/G]GGTCTCAATATGGTA	114804
rs533458946	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76173999	TGCAATTTGGGGCCC[A/G]AAGAGCCAGATTTAT	114804
rs533476615	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76191921	CGTGTAATCAACTGT[A/T]AAGCTATTTGACTCG	114804
rs533500922	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154053	TATCTCCTGCAGCAC[C/T]CGCACCTGACATCCA	114804
rs533548332	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76143286	CAGGAAGGGGGTCCT[A/G]GCCACTGTGGCTACT	114804
rs533549192	snp	A/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76193987	GACTCCCTGGACTAC[A/T]TGGGAACCAGGCCAC	114804
rs533614237	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76185134	TTGAGAATACTGAGA[A/C]TGGGCAACATGCTCA	114804
rs533620847	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76234681	TTGGAGAAATGTCTA[C/T]TCAAGTGCTGTGACC	114804
rs533633539	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76185629	CACCCGCTACCACGC[C/T]CGGCTAATTTTTTGT	114804
rs533664888	in-del	-/T/TT	0.290718	0.246662	intron-variant	RNF157	GRCh38.p7	17:76209482	TAAGATTTTTTTGCG[-/T/TT]TTTTTTTTTTTCTTT	114804
rs533682503	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76179222	CAACATGGCGAGACT[C/T]TGTCCCCACAAAAAA	114804
rs533706262	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76226389	GGAGATGGCCAATTG[G/T]GTTCACCATCTGGGG	114804
rs533746249	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241831	CCAGACTGGTCTCCA[A/G]TTCCTGACCTCCGCC	114804
rs533791266	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76175632	AAAATCCGACACAAA[C/T]GCTAGTCTATTCTAA	114804
rs533828442	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76169524	TGATCCTCCTGTTTT[G/T]GCCTCCCAAAGGTCT	114804
rs533841937	snp	A/C			upstream-variant-2KB	RNF157	GRCh38.p7	17:76240925	GCGTCCCAAAGCGGG[A/C]GGTCCCCGCTCCGCT	114804
rs533845540	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76227117	TAACCTCTTTTTTTG[-/T]TTTTTTTTTTTTTTT	114804
rs533856294	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76216094	ATATATTAGGTAAAA[C/T]TGGAAAAGTTAAAGA	114804
rs533888637	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76181432	ACAAAATCTTTGTCT[A/G]TAAGATCTAACAGTA	114804
rs533895325	in-del	-/TCTTT			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213610	ATATCCAAAGTGATG[-/TCTTT]TCTTTTTTTTTTGTC	114804
rs533896526	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76226953	TGGTGCTGCTGCCGC[C/T]GCTGCAAAGGCCAAT	114804
rs533956390	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76220240	CAGATAACAAGGACG[C/T]TCTCTAAACCTACTA	114804
rs534008528	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76222361	CAAAAAAAAAAAAAA[A/C]AAGTTCTAGAATAGA	114804
rs534042940	in-del	-/AA			intron-variant	RNF157	GRCh38.p7	17:76215555	TAAAAAAAAAAAAAA[-/AA]TGAGATTCAGTACTT	114804
rs534045288	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76182959	CTGTTGGTTACTTTT[C/T]GCTCTTGTTGCCCTG	114804
rs534077095	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76176141	CCATGCCAGGAGTAA[A/G]GAGAGATTGAAAACC	114804
rs534100493	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76233115	TTAGCAGAGACAGGG[C/T]TTCACCATGTTAGCC	114804
rs534109643	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76206704	CTGGACTGCAATGGC[A/G]TGATCTTGGGATCTC	114804
rs534112169	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76208243	CACTTTCAGATACCA[A/G]TATTTCAGAAATTGC	114804
rs534114091	snp	A/C			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149799	AGCACTTTGGGGGGC[A/C]GAGGTGGGCAGATCA	114804
rs534124917	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76214378	CCTATATCCGCAGAC[A/G]CACACATTTCTTTGC	114804
rs534145151	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76207402	CACTCCAGCCTGGGT[A/G]ACAGGGCAAGTCCCT	114804
rs534152026	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76219446	GAGTGGCTATGAAGA[C/T]ATATACATATTAATT	114804
rs534152363	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142694	GGACCCCAACTCCCA[A/G]GTGAGGTGGGCAGGA	114804
rs534185384	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76199966	TTTCAGGTCGGGCGC[A/G]GTGGCTCACGCCTGT	114804
rs534214613	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76209534	ACTGCTAGTGTATTC[C/T]GTGTGTGGCCCAATG	114804
rs534235613	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241186	CTAAAGTTAGGAGAA[C/T]ATCGACTGAGGATAA	114804
rs534247849	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76196969	CCACTGCCCCATCTG[C/T]CTTCCTCATCTCTAG	114804
rs534306780	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76167894	GTGGGCTTCTCTGAA[C/T]GATCATAAGCATAGG	114804
rs534347452	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76160805	CCTTTCCAATCCAAA[A/G]TCAACTAAATAATCA	114804
rs534359902	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76168526	CTCTCAAGACGTTCA[C/G]ATGCACCAAGCGGTC	114804
rs534366779	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76177455	CATGCTCGGGGTAGC[A/G]CTGACAAGCCAGCCC	114804
rs534378383	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76232077	GCATGTATCAGTAGT[C/T]TATCCCTTTAAATTG	114804
rs534418616	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76172062	GGTCGGGGGACTGTT[C/G]TGCAGCAGACAGGTA	114804
rs534425866	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76199076	GGTATTCCACAGAAT[A/G]TAAATGATTGAGGGA	114804
rs534473357	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76159120	AGAAAAAAAGAATAC[A/G]TAAGAGATTTGTCTC	114804
rs534477740	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76165890	ACTATGTTGGTCAGG[A/C]TGGTCTCAAACTCTT	114804
rs534502630	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76210385	GATCACGAGGTCAGA[C/T]CGAGACCATCCTGGC	114804
rs534527976	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76203913	GCTGGGACTACAGGC[A/G]CCCGCCACCATGCTC	114804
rs534535480	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76196306	ACACAGTTCCACTTA[C/T]ATAAAGTTCAAACCA	114804
rs534625513	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76194793	GGCCAAGGTGGGCAG[A/G]TCACGAGGTCAGGAG	114804
rs534658760	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76163317	CCTGTCTCAGCCTCC[C/T]GAGTAGCTGCGATTA	114804
rs534701815	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76171421	CTTGAACTCCTGACC[C/T]CGGTGATCCGCCCGC	114804
rs534739398	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76165440	CAGCAAACGGGTTAC[A/T]TGTGTCTCACACGAA	114804
rs534754847	in-del	-/C	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76183240	CCACGCCCGGCCTCA[-/C]GTGGGAATATTTTTG	114804
rs534835879	snp	A/C	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151794	ATAGAGGAGCCCTAA[A/C]TCGACCTCTCCGTTG	114804
rs534874832	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76144914	GCCTTCTTGTTCTAC[C/T]CCCTAAGGAGAAAAA	114804
rs534876205	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76197066	AACCTAAACCGGTTG[A/G]TATCAGATGTTGTCT	114804
rs534902917	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76189040	CTAAAAATTTTCAAG[A/G]TCATGAAGAACAAGG	114804
rs534904737	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153134	TCTCAGTGAAACAGA[C/G]AGAAGAAAACAAATC	114804
rs534944503	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153559	GGCTCCTGGAACACA[C/T]AGTGTTCCCTGCTTG	114804
rs534955719	snp	G/T	0.0130921	0.0798413	intron-variant	RNF157	GRCh38.p7	17:76182810	TATATATATGAGAGA[G/T]ATATATATCCTATAT	114804
rs534977521	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76190291	CTTGCCTCAGCCTCC[A/T]GAATAGCTAGGTCCA	114804
rs534992585	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76183228	AGGTGTGAGCCACCA[C/T]GCCCGGCCTCACGTG	114804
rs534996683	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76176902	AGCCACTGTGCCCAC[C/T]CTGCCGAGGGTGCCA	114804
rs535009026	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76208700	AACATTTGCCAGCGC[A/G]GTGGCTCACACCTGT	114804
rs535044217	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76160080	CCACCATGGCCTCCC[A/C]AAGTGCTAGGATTAC	114804
rs535050520	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145776	GTGAGAAGACTGTTC[A/G]TTCTGGCCGAGTGTT	114804
rs535052940	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76223376	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT	114804
rs535166831	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76154841	GACTGGGCTCCTAGA[A/T]GGGTGCAGTGGGCTG	114804
rs535204992	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76240044	GTTTCGGAGCGTCCG[C/T]AACCACTGAGTCCCC	114804
rs535226941	snp	A/G	0.000322376	0.0126919	missense, intron-variant, utr-variant-3-prime, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145321	GGCGCTGGGCATTCC[A/G]ACTGACGGCATTGTC	114804
rs535259785	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149000	TGCTTAGCGTGGTCT[C/T]GCAATTCTAGTCTTA	114804
rs535283435	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76193537	TTGGAAACAGCTACC[C/T]CCACCACCCCCCACC	114804
rs535292919	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142746	GCTTAGAGTGTGGTG[A/G]TCTGTGCCCAGGAGA	114804
rs535319326	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76229898	ATTAGGACAAAGAAA[A/G]GCTGGGGTTGGAGAA	114804
rs535330800	snp	A/C	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76179987	GGGAGTGCATGGTGA[A/C]AAGGAAGACCAGATA	114804
rs535350598	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76180831	TCACATTCGCATTAT[C/T]GTGCGGCCATCACCG	114804
rs535364303	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76174079	GAGAATTAATAATAA[A/T]AAAAAAAACCGCTGA	114804
rs535370783	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76180654	GGTCTCAAACTCTTG[A/G]GTTCAAGTGATCTTC	114804
rs535387805	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76230434	TATGCAAAGCATCCT[A/G]AGTCAAGACCTTAGC	114804
rs535421724	snp	A/C	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76205725	CAAGACTCCATCTCT[A/C]AATAAATAAATAAAT	114804
rs535439160	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76228679	TGTAATCCCAGCACT[C/T]TGGGAGGCTGAGGCA	114804
rs535460699	snp	A/G	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76206465	TAAGGGACCAGAGCA[A/G]AAAGACCTTCAGAAG	114804
rs535462317	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76198593	GCCGTATACGTCAGT[A/G]TCCTCTTCATTCCTT	114804
rs535485526	snp	A/C	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147390	TAAAAACAGCAGCAC[A/C]ACCACCACCACCGCC	114804
rs535518682	snp	A/G	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76196102	CACTGCCTTTGGGTA[A/G]CCCTGCTCTGCAGGA	114804
rs535537080	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76231935	TAGGCAAACACTATT[C/T]TGCTTTCTATCTCTA	114804
rs535556057	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76232552	TGAGCAATGCCGCTA[C/T]GAACATCTGCATCCA	114804
rs535565574	snp	A/G	0.0023933	0.0345097	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76148303	AGGGTCTCTTGCTCT[A/G]TCGCCCAGGCTGGAG	114804
rs535597471	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76225964	CTCCATTTTTTTCAG[C/T]TTCTTATCCAGTTTC	114804
rs535619072	snp	A/G	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76232952	TTGAGACACAGTCTT[A/G]CTCTGTCACCCAGGA	114804
rs535689141	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76218827	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGA	114804
rs535715844	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151681	GTGATTAACATGATC[C/T]TGTGTAAGGCATTAC	114804
rs535726892	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76233671	CCTGCCGAGTAGCTG[A/G]TATCATGCCACCATG	114804
rs535804108	snp	G/T	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76210996	TTTTAATAGAGATAG[G/T]GTTTCACCATGTTGG	114804
rs535815359	snp	C/T	0.00119737	0.0244387	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154149	GTACCATTAAGAAGA[C/T]GATCTTTCCTCTAAC	114804
rs535837578	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76191535	TGAACCCGGAGGTGG[A/T]GGTTGCAGTGAGCTG	114804
rs535838957	snp	A/G	0.00478085	0.0486577	intron-variant	RNF157	GRCh38.p7	17:76194843	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	114804
rs535864109	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76188213	CTCTATCATGCTCCA[A/G]CTCCAAGGTGACTTA	114804
rs535925003	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76178198	CTGTGGCCCGTCGGG[A/G]AGCCCAGACCTGGGA	114804
rs535927663	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76206292	ATTTCTAAGCCTCTA[A/T]TAACTTAGAGTTGGG	114804
rs535928681	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76228919	ACAGAGTGAGACTCC[A/G]TTTCAAAATAATAAT	114804
rs535937060	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76175687	TAAAATTTTTTTCTG[G/T]AGTAGCAAAGTTAAT	114804
rs535950268	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76194587	AGAAATGGCCTATGT[C/T]CTCTTCCATGATTGT	114804
rs535964322	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76178675	ATGCTGAGCTCTTTA[A/T]TTATATTATCTTATT	114804
rs536003582	snp	C/T	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76223091	GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG	114804
rs536004623	snp	A/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76217996	AAAGTTCTAGACATC[A/T]GTTGCAAAACAGAGT	114804
rs536019526	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76214511	ACTTTAACTTGCTGC[A/T]AACATTATTGTTTCA	114804
rs536131141	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76163406	CACCATGTTGACCAG[A/G]CTGGTCTCAAACTCC	114804
rs536134326	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76166605	AATCTCAGAAAGGGC[A/G]ATACTGTCAAGAAGC	114804
rs536195563	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76205069	TGGGATTAGAGGCGT[A/G]AGCCACCATGCCCAG	114804
rs536221697	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76181372	TATCTTTAACAGGAG[C/T]ATCTAAGGTCTTCTT	114804
rs536271973	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212538	CAGTCAACCTAAATC[C/T]AGTAAAAAAAAAAAG	114804
rs536280409	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76181600	TCTAAAATATGGCGA[C/T]TTCTTCACTAAATTG	114804
rs536293331	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76187013	TTGAGAAAAATAATA[A/G]TAGTATGAAATATAT	114804
rs536293425	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76228531	TTGCGTTCCTCTCTC[C/T]CCACTGGCTTCTTAC	114804
rs536295362	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76174539	GATTTCAAATGTTCC[C/G]GGTATTTTTAAAATG	114804
rs536312266	snp	A/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76181960	TTTCAAAAAACAAAG[A/T]CATTTACCCATTCAT	114804
rs536354342	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76176209	ATAAGGCAGCTGACA[C/T]AGTAATTGTAATATC	114804
rs536371743	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76161668	AAGGAGAAAACAGGC[A/C]ATCAGGACATCCTGA	114804
rs536422392	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76237273	CAATTTCAGCTGGAC[A/G]CTGTGACCGTCATTA	114804
rs536427814	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76200030	ATCACGAGGTCAGGA[A/G]ATCGAGACCATCCTG	114804
rs536469745	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76215173	AGCAGGCAGGGTGTG[A/C]TGGATCTTGCCTGTA	114804
rs536490787	snp	C/G	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76170060	CTGTGGGCTGACCTG[C/G]ATCTGTTGAGGAACC	114804
rs536490828	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76176807	AGGGCCAGGCCTGGG[C/T]GCGGAGCTGGGGCCA	114804
rs536502221	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194758	CGGTGGCTCACACCT[C/G]TAATCCCAGCACTTT	114804
rs536542068	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241891	CCACCGCGCCCGGCA[C/T]ATTTCGTATTTTTCA	114804
rs536561213	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76164124	CCTCACCCACCCTCC[C/T]TTGCCAATGCCACTG	114804
rs536607691	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76220989	TTAGCCGGCTTGGTG[A/G]CAAGGGCCTTGGTCC	114804
rs536690134	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76210982	GCTAATTTTTGTGTT[G/T]TTAATAGAGATAGGG	114804
rs536787448	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213305	GCCGGCATGGTGGCT[C/T]ATGCCTGTAATCCCA	114804
rs536793386	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157	GRCh38.p7	17:76155946	CCTTGGGGACAAGAC[A/G]TTTGCTTTTCCCTGT	114804
rs536796459	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76159089	TCTTCCCTATATCCC[A/C]TCCCCTATCCTTGAA	114804
rs536815418	snp	C/T	0.000259326	0.011384	intron-variant	RNF157	GRCh38.p7	17:76162510	CGATTTCTCACTTGG[C/T]CTCCTGGAAAGAGTA	114804
rs536818966	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76200942	TTTTCTGTCTTTCTC[C/T]GCAAGCCCCCAGACA	114804
rs536822381	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76204848	GGAGTACAGTGGTGC[A/G]ATCTCGGCTCACTGA	114804
rs536826309	in-del	-/CC	0.00478085	0.0486577	intron-variant	RNF157	GRCh38.p7	17:76183211	CAAAGTGCTGGGATT[-/CC]AGGTGTGAGCCACCA	114804
rs536896582	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76192049	TTTTTCTTTGAAATG[C/G]AAAACCAGTAAGTAT	114804
rs536987679	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76239377	TAAGTGAAGGGATGA[C/T]TCTAATAACAAACAT	114804
rs537007344	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76217049	AGCTTGAACACCTGT[C/T]CAATCACTCAATAAT	114804
rs537088115	in-del	-/C	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76156908	TCTCCATAATCCCTT[-/C]CCTTCCCTCCAGGCG	114804
rs537098700	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76174757	ACTTGGGAAACAATA[C/T]AGTTAAACCATAGTT	114804
rs537101278	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76189760	GGAGAAGGGACCCTC[A/C]GAAGCTGGGACTCAG	114804
rs537127785	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76165983	ACGCCCAGCTAAACC[A/G]CATTTTTTTGAGACT	114804
rs537147365	snp	C/T	0.000115495	0.00759831	missense, intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152451	CCATACCTAGAAATG[C/T]GCACGTCCTCTGGCC	114804
rs537148069	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76157887	GCCTCCCGACACCCC[C/T]CACTTACCCCCAGGA	114804
rs537164618	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76158561	AAAGAACAGAACTTA[A/C]TGCAAGGGGAGCTGA	114804
rs537173885	snp	A/C	0.00279162	0.0372561	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152910	CTCTGCAAAATAAGT[A/C]CATGAAACAACAACT	114804
rs537189055	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76204056	ACAGGCGTGAGCCAC[C/T]GCGCCCAGCCCATAA	114804
rs537204114	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76225634	TATGGCATGACCTCA[C/T]TGTTTTTAGTGGCCA	114804
rs537206784	in-del	-/T	0.0941369	0.195465	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144325	TTCAAGGGCTCCTTC[-/T]TTTTTTTTTTTTTTC	114804
rs537310816	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76177530	GAGGGAAGGGGAAGG[A/G]GGAGAGGCGAGGGGG	114804
rs537314165	snp	G/T	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76184189	GAGCAAGACTCCATC[G/T]AAAAAAAAAAAAAAA	114804
rs537381119	snp	C/T	0.00478085	0.0486577	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147405	CACCACCACCACCGC[C/T]GCCGCCACCACCAGC	114804
rs537391860	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76231994	TAAACAAACTCATAC[A/G]ATATATAGTCTTGCA	114804
rs537403149	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76157326	CTGGGTCTGTCTCCC[A/G]TCTAGTCCAGGCTGC	114804
rs537416090	snp	G/T	0.00194265	0.0311055	intron-variant	RNF157	GRCh38.p7	17:76240134	CCTCCTCGCGGCTGC[G/T]GCGCCCGCCCGCCCT	114804
rs537458060	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76202989	AAAATGCAAATTAGA[C/T]TGTAATAGTTATCTT	114804
rs537497192	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76196083	TGAGCCGCTACTCTC[A/G]ACACACTGCCTTTGG	114804
rs537527698	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241093	GGTGACCGGCTAGGA[A/G]GATGCCGCCTCCCTC	114804
rs537544590	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149237	CGGGAACCAACAAGG[A/T]TCGCAGTCCTTGCCA	114804
rs537561658	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76236996	AGAACCAGGTGGATG[C/G]ACAACAGCGGTGAGA	114804
rs537584308	snp	A/C/G	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149883	TGCTAAAAATACAAA[A/C/G]ATTAGCCGGGCGTGG	114804
rs537586352	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142834	CTCTGTGAGGAAGCC[A/G]GGATCACACCACCTG	114804
rs537624485	snp	A/G	0.00597247	0.0543191	intron-variant	RNF157	GRCh38.p7	17:76230499	AAGAGTTTCCTACCA[A/G]ATCTCTCTGCTTCCA	114804
rs537625434	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76143251	ACTAAGCACCTGCTG[C/T]GAGGAAGGACAGGGA	114804
rs537681974	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76183234	GAGCCACCACGCCCG[A/G]CCTCACGTGGGAATA	114804
rs537715946	snp	A/C	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76174709	TATAATCAAATTGTG[A/C]CCTCACAGGTTTTTA	114804
rs537789052	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76225226	TGCAATGGCTCACAA[C/T]TGTAATCCCAGCACT	114804
rs537800287	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76226024	CTCTCCAGGAGGATC[A/G]TAAGGTTTGGGGTGG	114804
rs537801909	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76206612	CGAGACCAGCCTGGA[A/G]CAACATAGTGAAACC	114804
rs537804056	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76232355	ATCGCACCACTGCAC[C/T]CCAGCCTGAGCACTT	114804
rs537829366	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76235200	TTGTAGTAGGTTACT[-/T]TTTTTTTTTTTTTTT	114804
rs537838158	snp	C/T	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76192853	TTCCTTTTTTTTTTT[C/T]TTTTTTGAGACAGCA	114804
rs537855573	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76193605	GGCTCTCTGAGATTC[C/T]CGGTTTAGGATCACT	114804
rs537860339	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76199764	CATGCTACTGGGACC[C/T]CGTCTCTCTGAAGAT	114804
rs537864546	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76226463	CAAGTGTCATCCAAC[A/G]TGGTCAAAAGGTCAT	114804
rs537894207	snp	A/G	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76193937	GCCCTGGGGGACACG[A/G]CTACCACTTCTCTGG	114804
rs537898853	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76187040	ATATCAATGGAAATA[C/G]TTAAGTTTATAAGCC	114804
rs537944091	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76155837	TCAGGCATTGAGGAG[A/T]GAAGTGGCCGTATCT	114804
rs538010956	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76220141	AAGTCATTCCCCACT[A/G]ACAGGAACAAGGGCT	114804
rs538080950	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76211673	GCTTATAAAATAGAG[C/T]GATAAGTCCTAAGTC	114804
rs538088092	snp	C/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76152052	AACAAGACTGGGCCA[C/G]CTGACATGGTACCTG	114804
rs538098571	in-del	-/T	0.00398564	0.0444627	intron-variant	RNF157	GRCh38.p7	17:76197871	GGAAGGAGTGAACTC[-/T]TAAGACTTGAGATGG	114804
rs538111976	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76181323	GCTTAGATGGCAGTA[C/T]GTACAAAATCATACC	114804
rs538119332	in-del	-/A	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76208809	AACCCCATCTCTACT[-/A]AAAAAAACACAAAAA	114804
rs538140104	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76232945	TTTTTTTTTGAGACA[A/C]AGTCTTGCTCTGTCA	114804
rs538170164	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76221734	AAGTACTATTTATAA[C/T]AATCAAAAGGTGGAA	114804
rs538171027	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76160715	ACTTTTAATTTTGGT[A/T]ACCTTTTAGACCTCT	114804
rs538226886	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76185289	ACCCAATCATGCTGT[A/G]CTTCTAGAATAAAAC	114804
rs538236723	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76189622	CTGGTTAAATGGATA[A/T]CAGAGAACTAAAACA	114804
rs538247295	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76182043	AAGAGTCAAGCAAAC[C/T]TCTCTTAGTTCCATC	114804
rs538333165	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76169651	ATGGCACGATCTTGG[C/T]TCATTGCAACCTCTG	114804
rs538346873	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76173425	ATAATTCTTCTTCCC[C/T]TTTAAAAAATATCCA	114804
rs538411131	in-del	-/T	0.391397	0.206172	intron-variant	RNF157	GRCh38.p7	17:76203453	AGGAAAAGTAAAAAC[-/T]TTTTTTTTTTTTTTT	114804
rs538433616	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76205994	CAGCACTCTCAGAGG[C/T]CAAGACAGGAAGACT	114804
rs538447464	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76210047	ACAGACATGAGTCAC[C/T]GTGCCCAGCAGAAAG	114804
rs538479159	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76173970	CAAGGTCACAGCTAG[C/T]GGGAAAACTGGGATG	114804
rs538480465	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76202344	GTGGCCTCTCACAGA[A/G]GCTGTTCCTTGGAGT	114804
rs538491111	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76195561	ACACAACAAAATACA[A/T]GTAATAATAGAACGT	114804
rs538517099	snp	C/T	1.66244e-05	0.00288304	intron-variant	RNF157	GRCh38.p7	17:76167832	GCATTTGCAGAGTAG[C/T]ATATCAATATTTTAA	114804
rs538525212	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76221388	CCAGTTAACCACCAG[C/T]TTATAGGGAATAAAA	114804
rs538536465	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76157353	CTGCACACTGCGGTC[A/G]GGTGGGCCTTTGGGG	114804
rs538539096	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76218941	CCATCTCAAAAAAAT[-/A]AAAAAAAAATAAAAA	114804
rs538576254	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76216606	AAAATAATAATAATA[A/G]TAATACTATGGTATA	114804
rs538631260	snp	C/G			intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153772	AACTTGGACCTGTCT[C/G]CTTGACCACGCCTTT	114804
rs538655784	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76182574	TTTGCTGTAAAAAAA[C/T]ATGGTCACAGTACAT	114804
rs538656826	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76208145	CCAGGCTGGTTTTCA[A/G]TTTCTAGGCTCAAGA	114804
rs538720277	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76200559	TGGAGGCCAGAGGCT[A/G]GTAGGAGAGGGAAAT	114804
rs538734246	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76198919	CTGCAGTGCACACAC[C/T]GTCTGTTGGTGAGAT	114804
rs538764502	snp	A/T	0.00953873	0.0683987	intron-variant	RNF157	GRCh38.p7	17:76163170	ACATGCAGCAAAATT[A/T]CACCTCTTGGCCCTG	114804
rs538778366	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76156577	TCTGCTGCGGCCATA[C/G]AAAGACTGCAGCTCG	114804
rs538809658	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76184748	AAGATATGAGGGAGA[C/T]AGCAAGAGAGTGTCA	114804
rs538877888	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76171251	TGGAGTGCAGTGGTA[C/T]AATCTCGGCTCACTG	114804
rs538879631	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76164288	AGAATGGATGGCTAA[C/T]TTTGAATTTTAGAAA	114804
rs538898606	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76188796	CTAACGAATACATCA[C/T]GGAAAGGGGAAGATT	114804
rs539002177	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76228984	ACTCACCCATCCATC[A/G]ATTCATCCTGTCCTT	114804
rs539023061	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213486	GAGGCAGGAGAATCT[C/T]TCGAACCCGGGAGGC	114804
rs539057273	snp	A/T			intron-variant, utr-variant-5-prime	RNF157	GRCh38.p7	17:76175766	CATTTCAAAAAAAAG[A/T]TGCGTCTTTTCCCTT	114804
rs539085533	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76208689	TGTCTTTTAAAAACA[C/T]TTGCCAGCGCGGTGG	114804
rs539137468	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76242019	ATTGGCTGCTGCTAA[C/T]GAAGGCTTGGGTTAC	114804
rs539188017	snp	A/C/T	0.0301464	0.119014	intron-variant	RNF157	GRCh38.p7	17:76224719	ATAGCTGATAAGCTT[A/C/T]AAAAAAAAAAAAGAA	114804
rs539193068	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150964	TTAGAAAATAAACAA[A/C]CCAGACAGACAGATT	114804
rs539216305	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76154791	CCATGGTCAGGGCAC[A/G]TCTCACACTGAACTG	114804
rs539247166	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76192107	GACAACAGGAAACAG[A/C]GGTGAGAGTGTGCAC	114804
rs539313722	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76216432	GATGTGTAGAGCTAA[G/T]TGTAGTTTTGCCTTG	114804
rs539320910	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76235338	GAGTAGTTGGGACTA[C/T]AGGCTTCTGTCACCA	114804
rs539321723	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76186091	AATTACTAAGGGCAA[A/G]AGGACCAAAATCTTC	114804
rs539368241	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76175379	AATTACAGGATCAAA[A/G]AGTAAGCATATTTTT	114804
rs539411646	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76237103	TAATTCTAAATAATT[A/T]AGGCTATTTATTTCT	114804
rs539440769	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76205062	AAAGTGCTGGGATTA[C/G]AGGCGTGAGCCACCA	114804
rs539486554	snp	C/T	0.00318978	0.0398085	intron-variant	RNF157	GRCh38.p7	17:76196965	TGCTCCACTGCCCCA[C/T]CTGTCTTCCTCATCT	114804
rs539539598	snp	A/G	3.29538e-05	0.00405904	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154341	TCCCTAGGACAGAAG[A/G]AAGGCCCTGTGAGTC	114804
rs539542198	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76238683	GCCATGTGGTTTAAG[A/G]AAAACAGAGCCCACA	114804
rs539546906	snp	C/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153492	CCGGGCATACGTGTG[C/G]TCTGGAGGTGCCCCT	114804
rs539577949	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147543	GCCAGGGCAGAACAT[C/T]GGTTACTTGTGGAAG	114804
rs539578938	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146552	GGCATGTCGTCCTCC[A/G]GACCCTGTGGGCCTC	114804
rs539595930	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76203217	GCTGGTCTCAAACTC[A/C]TGGCCTCAAGCAATC	114804
rs539608182	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76239465	CCAGGCTTGCCACTA[C/T]GCTAGCAAAGGGGCA	114804
rs539710967	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76178531	TGAGCTGAGTGCAGC[C/T]TGTCAGGCCAAGTGG	114804
rs539723874	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76232535	CAGTTTCTTGGCTAT[C/T]ATGAGCAATGCCGCT	114804
rs539765022	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76166127	TTAGAGGTGCACACT[A/G]CCATACCCAGCTGAT	114804
rs539779412	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153023	TGAGTTGTTATTTTC[A/G]GTGTGTTTTAAGTGG	114804
rs539786520	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76232924	CTATTGAAATCTCGC[A/G]TATTTTTTTTTTTTG	114804
rs539821205	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76196143	AGCTGTAACACTGCC[A/G]CCTCAATAAAGCTGT	114804
rs539876976	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76190415	CAAGTGATCTGCCTG[C/T]CTCAGCTTCCCAAAG	114804
rs539913584	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76191339	AAATTAGGGCTGGGC[C/G]CGGTGGCTCACACCT	114804
rs539915164	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76183364	CAATTCTGATGCAGG[C/T]AGGTTAGAGACCCCA	114804
rs539925560	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76174196	GCAAGCCCTTTCCTT[C/T]GGTGAGGCCATGCGG	114804
rs539967613	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76225871	GTTCTTCTTTTCCAG[A/C]TCTTTGCACTCGCCA	114804
rs539970395	snp	G/T			intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153541	CAGCAGGGGGAAGAG[G/T]CTGGCTCCTGGAACA	114804
rs540054905	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76217140	AAGATTGTATGAATT[A/T]AAAAGAGCTCCCCAA	114804
rs540072135	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76178192	GAAGAGCTGTGGCCC[A/G]TCGGGGAGCCCAGAC	114804
rs540084860	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76161425	GCTAAATACTGCAGC[A/G]TGCCCTGGTCTAATT	114804
rs540108733	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76172143	TAGCTGGGGAACCAG[C/T]AGAAACTTCAGGGAC	114804
rs540152057	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157	GRCh38.p7	17:76156145	CCCTTCCCGGAAGAA[A/G]CACCAGGACACTGTG	114804
rs540181681	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241522	TTTTCAACAGTGTTC[A/G]AAGTACAGTTTGGGG	114804
rs540191634	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76210539	AGCTTTCAGTGAGCC[A/C]AGATCGTGCCACTGT	114804
rs540192730	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76211048	AACCTCAGGTGATCT[A/G]TCCACCTCGGCCTCC	114804
rs540194690	snp	C/T	0.00438332	0.0466095	intron-variant	RNF157	GRCh38.p7	17:76181705	CTGAGGTCCAGAGTT[C/T]GAGACCAGGCTGGCC	114804
rs540201225	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76200179	CCTGGGAAGCGGAGC[C/T]TGCAGTGAGCCAAGA	114804
rs540228316	snp	A/G	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76187120	GGCTATGTATTTGCA[A/G]ATACAGCCCTGGGAA	114804
rs540268351	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76180150	CAGTATGGATTTATA[C/G]AATGGCTTCCTGTTT	114804
rs540369129	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76221276	AGACAACCAGATACA[C/T]GCTAGTGACAGCAAA	114804
rs540384623	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76205093	TGCCCAGTCTCCTTC[C/T]TTCCTCCCTCCCTCG	114804
rs540426794	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76154983	AATATATTCTCAAGG[C/T]CAGGGGCTGGCCAGA	114804
rs540451580	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76198724	AGAGATCTTTTAAAA[C/T]GTGTCTTCTGTGAGC	114804
rs540469352	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76168794	GGTGTGTTGGGAAAT[A/G]AACTTTTGAGAGCTA	114804
rs540492241	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76193178	CTCTGAGCATCAATG[C/T]CCTTATCTGTAAAAT	114804
rs540517898	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76179430	AGCGTGGTGGTTCAT[A/G]TCTCTAATCCCAGCA	114804
rs540519144	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76188782	TTAGTGACTGGCTTC[C/T]AACGAATACATCATG	114804
rs540523790	snp	C/G	0.0490535	0.14873	upstream-variant-2KB	RNF157	GRCh38.p7	17:76240634	CGCGCGGGGAGCCGC[C/G]GCTGGACTCGGCGCG	114804
rs540551687	in-del	-/T			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76148008	TAAATATAAGGACTG[-/T]AATAGTTCAACTGTC	114804
rs540556461	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, downstream-variant-500B	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142040	AATTCTCCTAGCGGG[A/G]TCATTTGCCCAATTA	114804
rs540578003	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150825	GCTCACAGCCCCACG[C/T]GAGCGCCTCCCAGGT	114804
rs540623448	in-del	-/A	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76168082	TAGTTTCCTCAAGGC[-/A]AAAAACAGCAGGCCT	114804
rs540630662	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76201857	CACTATAATGGCCAT[C/T]AGATATTTTCTAATT	114804
rs540645589	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76209782	TTTGTTTTTTTGAGA[C/T]GGAGTCTCACTCTGT	114804
rs540676016	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76166773	GCATGGCTTTCTCAA[A/G]GTATCCTAGGCTAAT	114804
rs540716417	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76167230	ATCAACAGGGTCTAG[C/T]GAAGAGAAGAAAGGG	114804
rs540750995	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76160349	AATGTTTTTAAGGCC[C/T]TGATATATACTGCTG	114804
rs540765608	snp	C/G	0.0825414	0.185628	intron-variant	RNF157	GRCh38.p7	17:76198281	AGCCTGTTGATACAG[C/G]GACATTCTCTTATGA	114804
rs540806460	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76193969	GTACACGTCCACAAA[C/T]GGGACTCCCTGGACT	114804
rs540813001	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194940	GAATGGCGTGAACCC[A/G]GGAGGTGGAGTTTAC	114804
rs540877867	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76230138	CAGCAAACTGGATCA[C/T]GGGAGTCAAAATGAT	114804
rs540887717	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76186531	AAACAAAACGAAACA[A/G]AAAAACCCCAAAAAA	114804
rs540938620	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76230646	AGTTTGAGACCAGCC[C/T]GACCAACATGGTGAA	114804
rs540945347	snp	A/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151561	CGTGAAACCCGGAGG[A/G]GACATTTGACTCAGT	114804
rs540978820	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76223688	AAACGTTAAATATTG[G/T]GTTTTACATATCTAG	114804
rs541007126	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76157944	GGGCCCTCTCTCCTC[A/G]TATATCTGCATAGCT	114804
rs541021576	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150036	AGACTCTGTCTCAAA[A/T]AAAACAAAAAACAAA	114804
rs541075751	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76163543	CCAATCCCACTCCCA[C/T]TAACCTGGGCCATGT	114804
rs541112866	snp	C/G	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76157220	ATCCGCCCGCCTCGG[C/G]CTCCCAAAGTGCCGG	114804
rs541158704	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76143705	GCAGCCACACAGAAA[C/T]GAAGGACCCCCTGGG	114804
rs541176318	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76230904	AGAGAAAGAGAGAGA[A/G]AGAGACTTTTCTTAG	114804
rs541236149	snp	C/G	0.00597247	0.0543191	intron-variant	RNF157	GRCh38.p7	17:76222156	TTCGAGACCAGCCTG[C/G]CCAACATGAAGCAAC	114804
rs541252487	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76236407	GCTTCATAAAAGCAA[A/C]CATCTCCGCAAAGCC	114804
rs541282124	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76182949	TTGTATACTTCTGTT[A/G]GTTACTTTTCGCTCT	114804
rs541308339	snp	A/C	0.00318978	0.0398085	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145489	CGATGACGGTGCGAG[A/C]CACAGCACTCGTGTG	114804
rs541346971	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76214018	AAATGTGTTTCTCTA[A/G]TTCTGTGAGTCCCTC	114804
rs541443160	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76185015	AGGGTACGAAAAACC[C/T]ACCACAGAGTAAAGA	114804
rs541451838	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76242181	AGCACACACAGGCCC[C/T]ACCTTGTAACTGCTG	114804
rs541475323	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76234241	TGCCAAATAATATTC[C/T]ATTGTGCAGACTTAC	114804
rs541476936	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76192251	ATGGCATCAAACAAC[A/G]AAGCAAAAGTTCAAG	114804
rs541493625	snp	C/T	0.00597247	0.0543191	intron-variant	RNF157	GRCh38.p7	17:76238850	TAAAATACTAACGAC[C/T]CACAGCTTTATCTTA	114804
rs541550628	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147642	CAGCAAGCGGGGGGC[A/G]CCTTCCCCTGGCAAG	114804
rs541597576	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76205468	GCCAGCGGCTGAGCG[C/T]AGTGGCTCAGCCCTT	114804
rs541613154	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76179077	TCAATACATGCACCA[C/T]TACTAAGTTATATTT	114804
rs541649747	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76179402	ATCCCAAAAAGGAAA[A/T]AAAAAGAGGCCAAGC	114804
rs541649874	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76173120	TGAAACCCCGTCTCT[A/G]TTAAAAATACAAAAA	114804
rs541684043	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76176469	CATTCTTCTGTAAAT[C/T]GATTTTGCCTACTAT	114804
rs541758793	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76167307	TTTCTATTCAACCCA[C/T]ACATCCAAAGAAAGG	114804
rs541759793	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147011	GTCTCTGGTGCTTGA[C/T]CCCAGGGGAACAGTG	114804
rs541943538	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76233209	ACAGGCGTGAGCCAC[C/T]GTGCCTGGCCTCTTG	114804
rs541944249	snp	C/T	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76232180	TCAAGACTAGGAGTT[C/T]GAGACCAGCCAGGGC	114804
rs541980241	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76218328	AAGCCCCTGAGCTCA[C/T]CTGAGGAGTCTACTA	114804
rs542016291	snp	A/C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76210397	AGATCGAGACCATCC[A/C/T]GGCTAACACAGTGAA	114804
rs542067859	snp	C/G	1.65222e-05	0.00287417	intron-variant	RNF157	GRCh38.p7	17:76158377	CACCCAAGAAGAGGA[C/G]AGGAATGTCAATTAC	114804
rs542081269	in-del	-/AGG	0.0138799	0.0821421	intron-variant	RNF157	GRCh38.p7	17:76210381	GCGGATCACGAGGTC[-/AGG]AGATCGAGACCATCC	114804
rs542092732	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76210584	GACAGAGCCAGACTC[C/T]GTCCAAAAAAAAAAA	114804
rs542106278	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76166202	CTGGTCTCGAACTCC[C/T]GACCTCAGGTGATCC	114804
rs542234044	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76177193	GCTGCAAGGGGGTGC[C/T]GCAGGGGCTGCATGC	114804
rs542235744	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76183525	GTGGCTATTCACTGT[A/G]ACCATAGTGCACTAC	114804
rs542278719	snp	G/T	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76177713	TGAGGCCCATAAAAG[G/T]CCCAGGCTCAGCCAG	114804
rs542299614	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76221951	TATGATTCCATGTAT[A/G]TGAAATATCCAGATA	114804
rs542320704	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76165732	GCCTGGGCTGGAGTG[C/T]GGTGGCATGATCTTG	114804
rs542323228	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76168923	TTTTTCACCTCCCAG[C/T]GTTGCTCCCAAGAAG	114804
rs542345657	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212920	GAGCAATTTCTAATC[C/T]CAGAGTGTTTTCTTT	114804
rs542359983	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76162331	GGCCCTGGTGGAAAC[C/T]GAGTTGGACAGAGCT	114804
rs542384380	snp	A/G	0	0	intron-variant	RNF157	GRCh38.p7	17:76207867	CAGATGGAATTACAC[A/G]TGGAATACGAACTCT	114804
rs542421311	snp	G/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76210398	GATCGAGACCATCCT[G/T]GCTAACACAGTGAAA	114804
rs542526562	snp	C/T	0.0158469	0.0875917	intron-variant	RNF157	GRCh38.p7	17:76157115	GGGACTACAGGTGCA[C/T]GCCACCACACCTGGC	114804
rs542532822	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76168452	TTTTTCTTCCAGTTG[C/T]GTAGTTTCCTATGTA	114804
rs542538268	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76197877	GAGTGAACTCTAAGA[C/T]TTGAGATGGGAACGT	114804
rs542548683	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	RNF157	GRCh38.p7	17:76242327	CTTCCTGCCCTCGGC[A/C]TTTTGTAAACGGGAC	114804
rs542562709	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76235077	TAGTAATTATATGCA[C/T]AGTAACTTTTAAAAT	114804
rs542571623	snp	A/C	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76199151	GAGGGGAAAGAAGAT[A/C]AAAGTTGGCAACATG	114804
rs542580721	in-del	-/CTTT	0.00318978	0.0398085	intron-variant	RNF157	GRCh38.p7	17:76165276	ATTATCCAGTCTAGC[-/CTTT]CTTTCTTTTATTTAT	114804
rs542585870	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76197416	GCCTGTAATCCCAGA[A/G]ATTTGGAAGGCTGAG	114804
rs542594319	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76156813	CCACACCCCCACCTC[C/T]GATCCCAGCCCCGAC	114804
rs542633063	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76181038	ACAGATAAAGAAACC[A/G]AGACTCAAAAGATTC	114804
rs542693685	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76160463	AAAGCAGGGAGAATC[A/G]CTAAAAAGAAAAGTT	114804
rs542707477	snp	C/T	0.00398564	0.0444627	intron-variant	RNF157	GRCh38.p7	17:76169637	CAGGCTGGAGTGCAA[C/T]GGCACGATCTTGGCT	114804
rs542708378	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76175730	TACAGGTACTTGGGC[A/G]TTATCCATAACTCCT	114804
rs542715097	in-del	-/CAT			intron-variant	RNF157	GRCh38.p7	17:76200411	AAGGAAATTCTGACA[-/CAT]CATGCTACAACATGG	114804
rs542768607	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76208287	CACAATGGACTCACA[A/T]ACAGGATGTGGGCAG	114804
rs542775585	snp	C/T	0.180383	0.240111	upstream-variant-2KB	RNF157	GRCh38.p7	17:76240713	GACTCGCGACGGGGA[C/T]GGGGGCGCGGCCGGG	114804
rs542832782	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76193724	ACGTGACTTCTGAAG[C/T]CTGATCCGAAACAAT	114804
rs542845553	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76200921	TCCTCCCCATGCTTA[C/T]TCTGGTTTTCTGTCT	114804
rs542871341	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76187214	CTTAAGATGGAGTCT[C/T]GCTCTGTCACCCAGG	114804
rs542887671	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76233326	AATATTTTCTTTCAG[A/G]AAGTGGCTTGTCTTT	114804
rs542925494	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76227734	AATACAAAATTAGCC[A/G]GGCGTGGTGATGCAG	114804
rs542925582	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76220546	TAGATGAGGGGAGGC[C/T]GGGTACCATGGCTCA	114804
rs542927729	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151255	TTAGAACAAACTAAA[C/T]AGAAAATGACTCAAG	114804
rs542937773	snp	A/G	0.00993419	0.0697739	intron-variant	RNF157	GRCh38.p7	17:76181670	CCCAGCACTTTGGGA[A/G]GCCGAGACAGGCAGA	114804
rs542969861	in-del	-/A	0.067446	0.170804	intron-variant	RNF157	GRCh38.p7	17:76184190	AGCAAGACTCCATCT[-/A]AAAAAAAAAAAAAAA	114804
rs542984349	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194812	CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA	114804
rs543046826	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76167949	ACAGAGTGCTTCATG[A/T]CCCATGTTGCTGGGC	114804
rs543051579	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76203557	TCCTGGGTTTAAGCA[A/G]TTCTCCTGCCTCAGC	114804
rs543090436	snp	C/T	4.94654e-05	0.00497295	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76165505	AAAGTCACTCACCTT[C/T]TCAAAAGTACCCAGC	114804
rs543094042	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76160983	TAGCTAACTAATTAT[C/T]CCAATACCATTCACT	114804
rs543098102	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76239764	GACCCCGCGAGGCAG[A/G]TAGGCTTTGGGCCGG	114804
rs543129407	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76158269	AAACCTTTGCCACTG[C/T]CTCAGAGGGTGCTGA	114804
rs543146726	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76193229	ATCTCATAGGGTCAT[C/T]AAGATCAAATAAAAA	114804
rs543219101	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76237989	CTTGGGAGACTGAGG[C/T]GGGAGAATTGCTTGA	114804
rs543223705	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76194137	TTCTGTGAATTTTGA[C/T]AAACACACACAACAG	114804
rs543226235	snp	C/T	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76191579	GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC	114804
rs543277780	in-del	-/T/TT	0.407674	0.194008	intron-variant	RNF157	GRCh38.p7	17:76232926	TTGAAATCTCGCATA[-/T/TT]TTTTTTTTTTTTGAG	114804
rs543288803	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76224829	ACATGTAGCCCAGCC[C/T]ATGGGGCGTGGGTTG	114804
rs543294096	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76180301	AACAAAGAATGAAAT[A/T]TGGTCTGCTCAGGGA	114804
rs543303073	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76184603	CAGAACAACAATGAT[C/G]TATATTAACTGCAGT	114804
rs543332839	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149982	AGGTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC	114804
rs543352393	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76225757	TACCCTCAACTAGGG[A/G]ACCCTTTTCTTCCCC	114804
rs543374305	snp	A/G	0.00914312	0.0669923	intron-variant	RNF157	GRCh38.p7	17:76229643	CTTCTGGAAGGAGGA[A/G]GAATCAAGGGCACTT	114804
rs543427613	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76188408	CTTCCTCTTTTTACT[A/G]ATTTTCTGCATTTCA	114804
rs543508455	snp	C/T	0.00318978	0.0398085	intron-variant	RNF157	GRCh38.p7	17:76237424	TCTGGAGAAAGCTGA[C/T]TCTGCCACTTGCTTT	114804
rs543528244	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152652	GCATGTCTGTGTTCT[C/T]GCGCTTTCCTGCTGT	114804
rs543539452	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194811	ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT	114804
rs543562069	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76230040	ATCATTAGTAAAATC[A/C]ATATTCTGAATATAT	114804
rs543566306	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153215	TCTTAGAAGCAAATA[C/T]TCTATGGGAGAAACA	114804
rs543603049	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146163	GCTCACTTCCTGGCC[A/G]TGTTGTGACTCCATC	114804
rs543603623	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76176581	GCTGTCCAGAGCAGC[C/T]GCTGCCATCACAACG	114804
rs543611554	in-del	-/TC	0.02016	0.0983543	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76148292	TTTTTTGAGACAGGG[-/TC]TCTTGCTCTGTCGCC	114804
rs543618502	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76183565	CTACTGGGCTCAAGT[A/G]ATCCTCCTGCCTCAG	114804
rs543639832	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76170371	GTAGCTGGGACTACA[C/G]GTGTGCACTACCATG	114804
rs543642598	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76202144	CACACACACACACAC[A/T]CACACACACACACAC	114804
rs543649024	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76182834	CCTATATATCCTATA[C/T]ATGATATATAGGATA	114804
rs543672641	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76171077	TTTTGTATTTTTAGT[A/G]GAGACGGGGTTTCAC	114804
rs543696122	snp	C/G	0.00597247	0.0543191	intron-variant	RNF157	GRCh38.p7	17:76177764	CACCAGCTGCAGAGA[C/G]GAGCAACCTACTCCA	114804
rs543740667	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146768	TCACTGTTGCAGTCC[A/G]GAGCCCAGCACAACA	114804
rs543764509	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76217421	GCAGCTTGCTTTCAT[C/T]TAGACAAATGAGAAA	114804
rs543766199	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76235478	GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCC	114804
rs543815592	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194908	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGC	114804
rs543825415	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76232624	TCATAGGAGTGGAAC[C/T]GCTGAATCATAAGGC	114804
rs543922413	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76193549	ACCCCCACCACCCCC[A/C]ACCCACGGACACATA	114804
rs544005025	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76223435	TCAGGTGATCCATCC[A/G]CCTCGGCCTCCCAAA	114804
rs544032927	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76167403	CCAAGATGGCACAAT[C/T]TGAAGGGAAAAGGTA	114804
rs544098303	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76164548	TCCTTTCAGGCCACC[C/T]AAGTCGTTTGTAATA	114804
rs544114709	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76215575	GATTCAGTACTTTGA[A/G]CCTGTGGAGAAGCCA	114804
rs544132039	in-del	-/TTC	0.0115144	0.0749975	intron-variant	RNF157	GRCh38.p7	17:76209556	GGCCCAATGTGACAA[-/TTC]TTCTTCTTCCAATGT	114804
rs544144589	snp	G/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76209809	CTGTCGCCCAGGCTG[G/T]AGTGCAGTGGAATGA	114804
rs544150117	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76217405	GAAATGAACCCCTCT[A/G]GCAGCTTGCTTTCAT	114804
rs544193348	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76185620	GACTACAGGCACCCG[C/T]TACCACGCCCGGCTA	114804
rs544194761	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76236415	AAAGCAACCATCTCC[A/G]CAAAGCCATACCTTT	114804
rs544212987	snp	A/C	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76218119	TATCAAGAAAAAAAA[A/C]CAAAAGGTATGAGCC	114804
rs544227877	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76207010	GTTACAAAGAGTTTA[A/C]TGGTAAGATATAAAT	114804
rs544285807	snp	A/G	0.00993419	0.0697739	intron-variant	RNF157	GRCh38.p7	17:76181679	TTGGGAAGCCGAGAC[A/G]GGCAGATCACCTGAG	114804
rs544332373	snp	G/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76227124	CTTTTTTTGTTTTTT[G/T]TTTTTTTTGAGACGG	114804
rs544362728	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76226391	AGATGGCCAATTGGG[C/T]TCACCATCTGGGGGG	114804
rs544375298	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76220371	GTCTAAGTCAATGAG[C/T]TCGTAATGATATCTA	114804
rs544386809	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76180036	CATCCTGGCATATCC[A/G]GAAACAGGAAGAGCT	114804
rs544434022	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76211898	GTCATTCATTCAACA[A/G]TCATTTATTAAGGGC	114804
rs544465939	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76205175	ACAGGGTCATGCTCT[A/G]TAGCCCAGGCTAGAG	114804
rs544510105	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76239606	AAATGCCTGTTTGGC[C/T]TCCATCCTTCAGCAG	114804
rs544559257	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213918	TGCCCAGAGACGGCA[C/T]AGAAGCTCTGTGCCC	114804
rs544562172	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154543	ATTAGATCCGAGCCA[C/T]ATTACCCATATATGC	114804
rs544568097	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76173866	GCTTTACAGTTTGCC[A/G]AGAATAGCCCTAAGA	114804
rs544606808	in-del	-/AA			intron-variant	RNF157	GRCh38.p7	17:76201581	TTCTTGATATATCCC[-/AA]GAGTTACCATTGTTA	114804
rs544607622	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76210405	ACCATCCTGGCTAAC[A/G]CAGTGAAACCCCGTC	114804
rs544633228	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76163859	GGCCTGAGCCCAGGA[A/T]CTGTTTCCTCCTCTG	114804
rs544683525	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76166295	CACACTTTTCACATC[A/C]GCCCAGGAGCTTGGA	114804
rs544697203	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76158749	TAACTTGCCTGGCTC[A/G]AAACCCAAATCTTAA	114804
rs544722421	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76166682	AAGTTTGTTAACTGA[C/G]GGCCATCAGCTGCTT	114804
rs544740428	snp	A/G	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76204592	TTGCCACAAAGCTCT[A/G]TAAGTGCAAAACTCT	114804
rs544740799	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, downstream-variant-500B	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76141963	AGAAGCGCACTCACT[C/T]CTCTGGAGACAGCTG	114804
rs544773087	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76214789	AAATGAAATCAGCAG[A/T]CAGGGGCCAAAATTC	114804
rs544778541	snp	G/T	0.00318978	0.0398085	intron-variant	RNF157	GRCh38.p7	17:76163091	GGATGCAAAGGGCGA[G/T]AGCAAGACCTTGAGG	114804
rs544878955	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76204604	TCTATAAGTGCAAAA[C/T]TCTATGTTACAAATG	114804
rs544922835	snp	G/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145102	GTGAGGGATTGTGGT[G/T]ACAGGTTGTAACAGC	114804
rs544934170	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76195419	GGTGCTGGACATTCT[A/G]AACACTGCTAGTGGG	114804
rs544995207	snp	A/G	1.6519e-05	0.00287388	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152468	CACGTCCTCTGGCCT[A/G]TAACGGAGTTAATGC	114804
rs545031323	snp	A/C	0.00179665	0.0299182	synonymous-codon, intron-variant, utr-variant-3-prime, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145256	AGCCAAAGGGCCCCA[A/C]ACACAGGGCCTCGTC	114804
rs545059297	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194218	TCCCTTGTGCCCTCT[C/G]TAGTCAACTCCTCCA	114804
rs545059502	snp	A/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76199283	TCTCCCAGTGTACTT[A/T]TATTCCAAATTGGTT	114804
rs545066519	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76169707	GTCTCAGCCTCCCAA[A/G]TAGCTGGGATTATAG	114804
rs545081574	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76157694	TCCCATGTATATGTC[C/T]TGTCCCAGCCAGACC	114804
rs545106290	snp	C/T	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76163048	AGAAGAAGAAGTTGG[C/T]AAGGAAAAAGATGGG	114804
rs545117159	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76208884	GAGGCTGAGGCAGGA[G/T]AATCACTTGAGCCTA	114804
rs545138470	snp	A/G			upstream-variant-2KB	RNF157	GRCh38.p7	17:76241985	CTCAGGATGGTGGGA[A/G]CACATCCCTGTCATT	114804
rs545239471	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76227792	TCAGGCAGGAGAATC[A/G]CTTGAACCCGGGAGG	114804
rs545270490	snp	A/C	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151986	CAGGCAATCCTTCCA[A/C]GACCTTCGTAGAGAG	114804
rs545284187	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76189305	ACTCTGTTATCTTTT[C/G]TGATTCTTCTGTAAG	114804
rs545306728	snp	C/T	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76181205	AGTGTTCCAGGGACC[C/T]GAGCAGAGTTCGGGG	114804
rs545349539	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76158668	CTCCTGGGCTTCAGC[A/G]ATCCTCTTGTTGACG	114804
rs545400083	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76155148	CCCCTAGGAAGGCTT[C/T]GTCAGCGCAGCCTCC	114804
rs545427714	snp	A/T	0.00597247	0.0543191	intron-variant	RNF157	GRCh38.p7	17:76165301	TTTATTTATTTATTT[A/T]TTTTGAGACAGAGCC	114804
rs545445902	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76240837	TTTATCCCGGCTCGG[A/C]TTACCGCGCAGGGAG	114804
rs545466006	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76204190	ACTCACCACTCTGAG[A/C]GCCAAAAGCACACTT	114804
rs545501048	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149486	TCTCAGCCCCAGGAT[A/G]GAAAGCTGAACTTAC	114804
rs545502155	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76197350	AAATGAGTTTCAGGT[A/G]TAGCAATCAAAAATG	114804
rs545507089	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241414	CATTTGTGTTTTAAA[C/G]CTTCTATTTTCTTTG	114804
rs545540088	snp	C/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150014	CTCCAGGCTGGGCGA[C/G]AGAGCGAGACTCTGT	114804
rs545546627	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76234918	TTGTTGAAACCACTA[C/T]CCTTTCCCCATTCAA	114804
rs545574914	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76143610	CAGAGAGGGTTGGAC[A/G]ACAGGCCCCCCTCTC	114804
rs545586717	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76184854	TTTATAGTCTTCGAA[C/T]TCCTCTGCTAGGTCT	114804
rs545610427	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146864	TGAGAGAGGCCACTC[A/G]CAAGTGTCCAGGGTC	114804
rs545631309	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76185394	AAGGAGAAAAGCGTG[C/T]TCTTAATAAAGCAGA	114804
rs545634618	in-del	-/T	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76231431	TTCTCAACTTTTTAC[-/T]GTCTTTTGAGGCCCA	114804
rs545663691	snp	A/C	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76211125	TTCCAATCGGGCCAG[A/C]CTGGTTTCCTTATTT	114804
rs545665060	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76228444	AGGTTAACTTCTTCA[C/T]CTGAGTTCTCATTCC	114804
rs545691891	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76175888	TCCATTTTGAATATA[G/T]TTGATGATAACTGTG	114804
rs545711489	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144312	GGGGATTCTCAGATT[C/T]AAGGGCTCCTTCTTT	114804
rs545738738	snp	C/T	0.00119737	0.0244387	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153247	TCACAAGGGGTAACT[C/T]TAGAGCCTCAAGCAC	114804
rs545759557	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76226139	TAGGACTCTGGGCTC[A/G]TACAGATGCCACTAT	114804
rs545767485	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76196608	AAAAGCAAGGGCCGA[A/C]GTATGTACGGGAGTG	114804
rs545786402	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76173113	AACATGGTGAAACCC[C/T]GTCTCTATTAAAAAT	114804
rs545899583	snp	A/G	0.00398564	0.0444627	intron-variant	RNF157	GRCh38.p7	17:76171099	GGGTTTCACTGTGTT[A/G]GCCAGGATGGTCTCG	114804
rs545923736	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76231383	CATCCTTTATGTGAT[C/T]TGCAAATATTTTCTT	114804
rs545925488	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76217459	CAGCCTTTTTCAGAC[G/T]GAATAAAGCTTTCTA	114804
rs545990482	snp	C/T	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76177612	CCTGGCTGCCAGTCC[C/T]GCCCACTGGAGTGGG	114804
rs546016193	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76178392	CTGGGGCTGCCAGCC[C/T]CACAGCGGCAGCTGG	114804
rs546025191	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76224599	TGTTCTTCATTTTTA[A/C]GTTTTCCCCCTAGAG	114804
rs546061190	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76217677	TAAAGTACTTCTTTG[C/T]CTATTTGTTACCAGG	114804
rs546069839	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76165602	CACATCTTGATGCCC[A/G]TGACTTTCTCCAGTT	114804
rs546099901	snp	C/T			utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142474	TGCAGTTAGCTCTCC[C/T]TCCCTTGTAAACAGT	114804
rs546145141	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76230185	TGGCAATCCACAGAA[A/G]CCTTTGAGGGGGCAT	114804
rs546161364	snp	A/G	0.00318978	0.0398085	intron-variant	RNF157	GRCh38.p7	17:76222198	TAAAAATACAAAAAT[A/G]AGCTGGGTGTAGTGG	114804
rs546186169	snp	A/G	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76223036	GCTGGGACTACAGGC[A/G]CCCGCCACCATGCCT	114804
rs546214726	snp	A/G	0.00755907	0.0610114	intron-variant	RNF157	GRCh38.p7	17:76182871	ATATATATATCCTAT[A/G]TATCATAATAATATG	114804
rs546219057	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76189817	CTGGTTCTGGGTTTG[C/T]TGGGAGGAGAACACA	114804
rs546226622	snp	A/G	9.95702e-05	0.00705515	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76167039	CTCGGAGGGATCCAC[A/G]GTGTGGGAGGGCAGG	114804
rs546256925	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76223445	CATCCGCCTCGGCCT[C/T]CCAAAGTGCTGGGAT	114804
rs546291775	in-del	-/CGCTT	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76210734	TCACTCACCTACCTA[-/CGCTT]CAAGTCTTAAATATT	114804
rs546309875	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76168188	AATATACTTGGGTTA[C/T]TACTTCTTGATTTTT	114804
rs546313843	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76220619	TTTGAGACCAGCCGA[A/G]GCAACATGGCAAGAC	114804
rs546350100	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76197324	AAGAGGACTGTTTCA[C/T]TGAAAAGAGAAAATG	114804
rs546374409	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76209845	GCTTACTGCAACCTC[C/T]GCCTCCTGGGTTCAA	114804
rs546496088	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76158308	TTGATGAGTGAATGA[A/G]AGCAGAGGGACCTGA	114804
rs546516203	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76155133	CTGATCTAGGCATGT[C/T]CCCTAGGAAGGCTTC	114804
rs546520758	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76203603	GATTACGGGAACCCG[C/T]CATCATGCCTGGCTA	114804
rs546528998	snp	A/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151579	CATTTGACTCAGTCC[A/G]CTTGGGCAAGATGTG	114804
rs546531508	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76186727	GGCAGATAACCTGAG[G/T]TCAGGAGTTTGAGAC	114804
rs546544919	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76219829	AGTTTACAGTAATCA[C/T]ATTATTGGTGACAGT	114804
rs546569096	snp	C/G	0.0023933	0.0345097	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149890	AATACAAAAATTAGC[C/G]GGGCGTGGTGGCGGG	114804
rs546586056	in-del	-/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76168175	CACGTTTCTAAAAAA[-/T]ATACTTGGGTTACTA	114804
rs546589311	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76210953	GGGATTATAGGGGTG[C/T]GCCACCACCCCGGGC	114804
rs546647282	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76167636	GAAGTGGCTCTCCTG[C/G]TCTCCTGATCTTACC	114804
rs546651694	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76238268	AAGGTTTCAAATACA[A/C]AAAGGTTTGCTGACA	114804
rs546678649	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76227952	GAACCTGTGCTCTTA[A/G]CCATTATAATGTATT	114804
rs546701227	snp	A/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76211570	TTTGAGAAAAATGTA[A/T]ATAAAACCCTTAGAA	114804
rs546713173	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76239217	AAATAAAACTACTTG[A/C]AATTAAAAGTAAACA	114804
rs546747975	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76206323	CAGTAATTATCCCAA[C/T]AAAACAAGATCTAAC	114804
rs546757137	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154059	CTGCAGCACCCGCAC[C/G]TGACATCCATGGCTC	114804
rs546876992	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76232943	TTTTTTTTTTTGAGA[C/T]ACAGTCTTGCTCTGT	114804
rs546887472	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149657	TCTGCCTAGAGAGAC[A/G]TGCTTTTCCCTCTCA	114804
rs546913451	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76180824	GTAACATTCACATTC[A/G]CATTATCGTGCGGCC	114804
rs546915847	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76193800	CTGGGCAGGCTCTCC[C/T]GCATCCTGCAGTGAG	114804
rs546938884	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76179272	GGTGGCACACACCTG[C/T]AGTCCCAGCTACTCA	114804
rs546950222	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76178908	TATCTTTCCCCAAGA[C/T]GCTCTGGATGCAGCT	114804
rs547013459	snp	A/G	0.0023933	0.0345097	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153515	GTGCCCCTGAGGGAG[A/G]GGCCTCAGAGCAGCA	114804
rs547045566	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76194744	GAGCAGGCCGGGCAC[A/G]GTGGCTCACACCTGT	114804
rs547110333	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76235592	AAAACTTTTATAGTT[A/T]TTCGACAAAGACTTA	114804
rs547116773	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150829	ACAGCCCCACGCGAG[C/T]GCCTCCCAGGTGTGT	114804
rs547156130	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76192523	AGAATGAATACACGA[A/T]CAACAAGATCTTCGG	114804
rs547160950	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76191935	TTAAGCTATTTGACT[C/T]GTAAGTCTTTGACAA	114804
rs547192574	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76210455	ATTAGCCGGGTGTAG[G/T]GGCGGGTGCCTGTAG	114804
rs547204732	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76225932	TGGCGGTACCTAGTG[C/G]CTGCTGTCTTGTTTT	114804
rs547290013	snp	A/T			utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76143990	ACATGCTGCTGCCTG[A/T]ACTTAGCTCAAGGCT	114804
rs547364924	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76187476	GGCATGAGCCACGGC[A/G]TCTGGCCAGGATTTT	114804
rs547397925	snp	A/C	0.00835141	0.0640778	intron-variant	RNF157	GRCh38.p7	17:76180380	GGCACAGATCCCCCT[A/C]ATCTATTCATCTAAC	114804
rs547525867	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76174465	TTGATAATGATGAGA[A/T]AAAGAAAGGGGAAAT	114804
rs547572867	snp	G/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76220666	TATTATTTTTTTTTT[G/T]TTAGTTAGCTGGGCC	114804
rs547594993	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76181919	TCTCAAAAAAAAAAA[A/G]AAAAAAGAATAAATA	114804
rs547630355	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76182447	GGGCACACACGCATT[C/T]AGTCTGTGTGTGTGT	114804
rs547664706	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76176773	CCTTGGCCAGTGTCC[C/T]GCTTGCTCATGGAGC	114804
rs547669215	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76208072	AGGCATGCACCACCA[C/T]GCCTGGCTAATTTTT	114804
rs547669773	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76223035	AGCTGGGACTACAGG[C/T]GCCCGCCACCATGCC	114804
rs547669969	snp	A/G			intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153151	GAAGAAAACAAATCC[A/G]TTCCACGGGCTAGGG	114804
rs547711918	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76200372	TACAGTGTATCGATA[C/T]AATGGCATATTATTC	114804
rs547746433	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76172116	GAGTTGACCCTGGGG[A/T]GGAGAGAAGCATAGC	114804
rs547832952	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76178418	GCTGGCGTGTCTGAC[G/T]GCACAGTGGCCGGAC	114804
rs547878086	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76221549	CCAAAGTACAGACTT[C/T]ATTTTATTAAACCCT	114804
rs547918389	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76174197	CAAGCCCTTTCCTTC[A/G]GTGAGGCCATGCGGT	114804
rs547968601	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76175275	GTTTTACTTTTTTTC[A/G]CAGCTATAAATGTTG	114804
rs547971774	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76221339	TTCAAATTTTAAAGC[-/T]TTAAAAAAAATGAAC	114804
rs547992407	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76217701	TACCAGGAGAAACAC[A/G]TCACTCACAGATAAA	114804
rs548005260	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76169128	TCTGTTCTCTGTAGA[A/G]CCCGTTAGTTGGATG	114804
rs548097181	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76237058	TTTAAAGTTTGAACC[A/G]TGTGACTATATTACC	114804
rs548104957	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76197816	AAAGGATGAACTCTC[A/G]GCCTATACTAGTCTA	114804
rs548105210	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76205438	TGCCGGGCACATTTT[A/G]GTTCTTAAAATAATG	114804
rs548110663	snp	A/T	0	0	intron-variant, nc-transcript-variant	RNF157	GRCh38.p7	17:76156469	AGAGGCCGCAGCTTC[A/T]CTCTTCCGTCCTCAC	114804
rs548117651	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76239070	TATTCTACCAAAAAG[A/T]GACGAGGCTCTGCTC	114804
rs548179644	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76226890	CTGCTGCTGAATGCC[A/G]TGGGAAGCGCCATGG	114804
rs548207242	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76219853	TGACAGTATTTTCTT[C/T]CGAGAATGTGGCATT	114804
rs548243854	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76233714	TTAAAAACAATTTTT[G/T]TAGAGACAGGGTCTC	114804
rs548267006	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76216899	CTGTGTCAAAAAAAA[A/C]CAAAAACAAAAACAA	114804
rs548303766	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76225836	TTGGCCAGGGAATCT[A/G]CCCTCTCTTTTAGAG	114804
rs548319307	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76171167	AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACTG	114804
rs548355997	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76165952	CAAAGTGCTAGGATT[A/G]CAGGGATGAGCCACT	114804
rs548357175	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76165070	ACTTATGAATTAAAC[C/T]TTATCATAGGTGTGG	114804
rs548423564	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152778	AGAGCTGGGCAGAGG[C/T]CAGGCTGGTGAGGCT	114804
rs548449463	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153407	TGCACACCTCCAACA[C/G]TTCCCAAGCGATGGC	114804
rs548450826	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76220404	AAAAAAAAAAAAAAA[-/A]GGTTACCTTTGAAGG	114804
rs548469024	snp	C/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76159019	TTCCTTCAGTCTTCG[C/G]ACTAAGCAATGCTCC	114804
rs548481547	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76238444	AGGAGAGGATTATTT[A/T]TTGAGTGTGCTAATT	114804
rs548502627	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76196639	TAGTCATGTGCTGGC[A/G]TCCCAACCTTCCCCA	114804
rs548504271	snp	A/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76159674	AATGTTTTATATCTG[A/T]TCTTGGGGGGGTCTG	114804
rs548508653	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76218340	TCATCTGAGGAGTCT[A/G]CTAAGGAATAAGCTT	114804
rs548509715	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76183232	GTGAGCCACCACGCC[C/T]GGCCTCACGTGGGAA	114804
rs548614856	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146431	TCTCCTGCCCACAGA[C/T]GAGCTCCTCCCTCCA	114804
rs548640530	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76155154	GGAAGGCTTCGTCAG[C/T]GCAGCCTCCTGGCCC	114804
rs548645103	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76190962	CACACCTGTAGTCCC[A/G]GCACTTTGGGAGGCC	114804
rs548727208	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76202931	TTTCTGTCTCTCTGA[C/T]TCATTACCTATACTG	114804
rs548732060	snp	A/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76160676	ATTGTAAATAGTTTT[A/T]AAAAAAACACTATTT	114804
rs548764310	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76190297	TCAGCCTCCTGAATA[A/G]CTAGGTCCACAGGCA	114804
rs548796665	snp	C/T			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147775	TTCCAGAGCAGGTGC[C/T]GCCATTTTGTCTGGC	114804
rs548813095	snp	A/G	1.65201e-05	0.00287398	missense, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156242	GTGGATGACAGAGGC[A/G]TCCCTGTGCAAGACG	114804
rs548822596	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241013	GTCTTCGGAAATCTC[A/C]TGCAGGGGGGTAGGG	114804
rs548849951	snp	G/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150302	ACTGTGAGCCCACCA[G/T]AATCTCTAAATAGCT	114804
rs548850577	snp	C/G	0.000798403	0.0199641	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145782	AGACTGTTCGTTCTG[C/G]CCGAGTGTTAATGTT	114804
rs548908437	snp	A/T	0.00953873	0.0683987	intron-variant	RNF157	GRCh38.p7	17:76187602	TTTATTTATTTATTT[A/T]TTTTTTTCTGAGACA	114804
rs548933731	snp	C/G/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76194993	GCACTCCAGCCTGGG[C/G/T]GACAGAGCGAGACTC	114804
rs548936971	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76233712	TTTTAAAAACAATTT[C/T]TGTAGAGACAGGGTC	114804
rs548988584	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76174229	TCCCAGGAGTTTAGG[C/G]ACCGCAAATAAAAGA	114804
rs548989829	snp	A/G	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76168358	TGTGTCTGTATTACT[A/G]TGATTACACAAACTT	114804
rs548994084	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76143245	GAGAGGACTAAGCAC[C/T]TGCTGCGAGGAAGGA	114804
rs549011127	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76198988	TTCATGTTTCCTAGC[C/T]GTACAACTCCTTCAG	114804
rs549058639	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76196257	GTCACAAAGATGCTG[A/G]GTGAAAGGAGCCAGA	114804
rs549065880	snp	C/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76148869	GCCACTGTGCCCGGC[C/G]TATCTTTGCCTTTTT	114804
rs549083693	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76232250	AAAATTAGATGGGAG[C/T]GGTGGCATGTGCCTG	114804
rs549098259	snp	A/G			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212502	AGAGGAACAAACAAA[A/G]AAAATCAAACAAGCA	114804
rs549110136	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76192777	TGAAATGATTTAATA[A/T]AACAAGTATGATATC	114804
rs549115380	in-del	-/AAAAAGAG			intron-variant	RNF157	GRCh38.p7	17:76230855	AAAAAAAAAAAAAAA[-/AAAAAGAG]AGAGAGAGAGAGAGA	114804
rs549117830	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76148819	CAAGTGATCACTTGC[C/T]TCAGCCTCTCAAAAT	114804
rs549125643	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76199688	CACTGGTGATCTCAA[C/T]GTGAAGTGTGACTGC	114804
rs549130387	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76226899	AATGCCGTGGGAAGC[A/G]CCATGGCTTAAGCCG	114804
rs549138900	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76239354	ACAATCCAGAGGCTA[A/G]AGACATTTAAGTGAA	114804
rs549164417	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76193853	ATCTGAGATTAGCGC[C/G]TGGCCGAGGGCTGCT	114804
rs549190763	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241640	TTGAGACGGAGTCTC[C/T]CTCTGTCGCCCAGGC	114804
rs549242518	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76220074	AGGCCTAGAAACATA[A/G]ACCAACAAAGTAGGA	114804
rs549251307	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76206416	TTTATTTAACATTTT[A/G]TAACTGATTCACAGA	114804
rs549284409	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76143895	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGGAGG	114804
rs549287359	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76227518	ATGTTGCTATTTTCT[C/T]TTCATTTTATAGAAG	114804
rs549352826	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194975	AGCCGAGATAGCACC[A/G]CTGCACTCCAGCCTG	114804
rs549405193	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147391	AAAAACAGCAGCACC[A/G]CCACCACCACCGCCG	114804
rs549447594	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76154696	TTAAGATCCCAAACC[A/C]CATCCAGATCCTCCA	114804
rs549449277	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76211660	CCTCAGTTCTCTCGC[G/T]TATAAAATAGAGTGA	114804
rs549479459	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149989	AGTGAGCCGAGATCG[C/T]GCCACTGCACTCCAG	114804
rs549517767	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76218848	CTGAGGCAGAAGAAT[C/T]ACTTGAACCCGGGAA	114804
rs549518166	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76172632	AAAAAAAAAAAAAAA[A/T]AGGCGAGACTCTGTC	114804
rs549523024	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76148489	AGCCAGGATGGTCTC[A/G]ATCTCCTGATCTTGT	114804
rs549604329	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76236660	AAAAATCACCTAATG[A/C]ATAACATTATTCATT	114804
rs549617177	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76173345	GGATTTGATATTCTA[A/C]GTTCAAATTTCCCAT	114804
rs549617234	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76179719	TAAGTATCTTATTTC[A/G]ACCTAAAACCAGAGA	114804
rs549711031	snp	A/C/G			intron-variant	RNF157	GRCh38.p7	17:76185788	TTACTCCTTTCACAC[A/C/G]AGCAACCCATCCTCA	114804
rs549771010	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76189461	AGCTGCTTTGCCCTA[C/T]TAAGCCTCCATTTCC	114804
rs549773226	snp	A/G	0.00478085	0.0486577	intron-variant	RNF157	GRCh38.p7	17:76235640	AACTGTTCTTGCAAT[A/G]GGAAAGACCCATTTG	114804
rs549780073	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76175376	TGGAATTACAGGATC[A/T]AAGAGTAAGCATATT	114804
rs549819197	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76169214	TCTCTCTGGATTTTT[C/G]CTCTACTTTCTAGAA	114804
rs549885834	snp	C/G	0.00104021	0.0227821	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145228	GCCCAAGTGCAGAGG[C/G]TGGGGCTCAGACAGC	114804
rs549921597	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76181702	CACCTGAGGTCCAGA[A/G]TTTGAGACCAGGCTG	114804
rs549924917	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145512	CTCGTGTGTGAGAAC[A/G]GAGAGAAGCAGGTGC	114804
rs549938386	in-del	-/TG			intron-variant	RNF157	GRCh38.p7	17:76205818	TGAGGAAGAAGAAAC[-/TG]TGTCAATGCGGCCCA	114804
rs549953885	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76169870	ATAGGCGTGAGCCAC[C/T]GCACCTGGCCTAGTT	114804
rs549972636	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76201194	TCAAACAACATAGAA[A/G]AATATGAAGAGCCGG	114804
rs549984996	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213334	CAGCACTTTGGGAGG[A/C]TGAGGAGGGCGGATC	114804
rs550110686	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194871	ATACAAAAAATTAGC[C/T]AGGCGTGGTGGCGGG	114804
rs550110743	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76201905	ATGCTACAATATACA[C/T]TGTAAATAGGAATCA	114804
rs550161193	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76221665	TCTTCTAAAATAACT[A/G]TAAGAAATAAAATAC	114804
rs550220655	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76235324	TGCCTCAGCCTCCCG[A/C]GTAGTTGGGACTACA	114804
rs550220802	snp	A/G	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76237503	GGTTGATTCCTCTAT[A/G]GGGACTTCAATTATG	114804
rs550231445	snp	C/G	1.65004e-05	0.00287227	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76166497	CATGTACCACTAGAG[C/G]GTAAACTTCTCGGTC	114804
rs550231628	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76173189	TACTCGGGAGGCTGA[A/G]GCAGGAGAATGGCGT	114804
rs550258088	snp	A/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151386	CAGGCTGATGGAGAG[A/T]GGCAACCACAGAGGT	114804
rs550268412	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76166948	GCTGTCAGACCGAGT[C/T]CTAAGTAGCCCCTAG	114804
rs550275599	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76222175	ACATGAAGCAACCCC[A/G]TCTCTACTAAAAATA	114804
rs550300358	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76208536	CAAAAACTAGGTGTT[A/C]AAATGTTAGCCATCA	114804
rs550375892	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76223599	AACCATATAAAACCC[A/C]AATTTTTTTCTTTCT	114804
rs550379999	snp	A/C	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76163163	ATCCCCAACATGCAG[A/C]AAAATTACACCTCTT	114804
rs550420945	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76157035	GCAGTGGTGCGGTCT[C/T]GGCTCACTGCAACCC	114804
rs550473935	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76205554	AGATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	114804
rs550510043	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76192883	ATCCGCTCTCTTGCA[C/T]AGGGTGACTGCGATG	114804
rs550517660	snp	A/C/G			intron-variant	RNF157	GRCh38.p7	17:76178443	CCGGACCCCACTCTC[A/C/G]CTCACACACCCCTTG	114804
rs550517872	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76226299	CTGGAGTGGAGGACT[A/G]GACCCCTGGGGAAAG	114804
rs550532949	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76159817	TGGAAATTTGGAAAA[C/T]ACATAAAAGTAAAAG	114804
rs550554430	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76206065	TAAGACATTCTCTCT[A/G]TAGAAATTTTTTTTA	114804
rs550569920	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76154763	TCACTGTGAGCTGGC[A/G]TTCCACAGCACACCA	114804
rs550585055	snp	G/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76179170	AGGCTGAGGCAGAAA[G/T]ATCGCTTGAGCTTAG	114804
rs550667515	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153422	CTTCCCAAGCGATGG[C/T]CAGCGCTAAAGCAGA	114804
rs550675108	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76218419	GCCAAGGCAGGAGGA[C/T]TGCTTGAGCCCAGAA	114804
rs550761913	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76206168	CCTAGGAAGTCGAGG[C/T]TGCAGTGAGCTGTAG	114804
rs550764967	snp	C/T	4.95217e-05	0.00497578	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76158443	GCTGTGTCTCCGACT[C/T]GCTGCAGGAATGCTC	114804
rs550774505	snp	G/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76227120	ACCTCTTTTTTTGTT[G/T]TTTTTTTTTTTTGAG	114804
rs550808519	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146543	GGTAGGGAAGGCATG[A/T]CGTCCTCCGGACCCT	114804
rs550847072	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147129	ATGAGTCAAGGTGTT[C/T]TTTTTCACCTCTAAT	114804
rs550858534	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76155092	GGGAGCAGCTGCTCT[A/C]ATCTCTACCCACATT	114804
rs550861022	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76169460	TATTTTATATAGAGA[C/T]GGGGTCTCACTATGT	114804
rs550897939	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76195290	AGATCTTTTTCCAGA[C/T]ACCACGTAACCAGGA	114804
rs550901116	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76148081	AATTTTCCTTAGTGC[C/T]CACAAAGTGCAAGTA	114804
rs550909195	snp	C/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76239876	CGCGTCCCCGTCACG[C/G]GGCCGATTACAATGG	114804
rs550937528	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76231490	TTTTGTAGAGATGAG[A/C]TCTCACCACGTTGAC	114804
rs550983180	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76157897	ACCCCCCACTTACCC[C/T]CAGGACTTTCTCCTT	114804
rs551022994	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241742	GCCTCCCGAGTAGCT[A/G]AGACTACGGGCATGT	114804
rs551084291	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76242349	AAACGGGACATCCCT[A/T]CCCTTTGTGGGTTTA	114804
rs551115068	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76143982	TGCTGGCCACATGCT[A/G]CTGCCTGAACTTAGC	114804
rs551142172	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76196763	ACCTGATCCAAGAGT[A/C]TTCCTGATTCCCTAT	114804
rs551177919	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76184239	GTATATTGGGCAGAC[A/C]TTTAATATTTATGCC	114804
rs551181302	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76191048	AAAAAAAAGTTACGA[C/T]ATGGATTAGCAGAGG	114804
rs551183476	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76197472	GTTTGAGACCACCCT[A/G]GGCAACACAGCAAGA	114804
rs551186305	snp	C/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76231125	GTCTCAGCCTCCCAA[C/G]CAGCTGTGACTACAG	114804
rs551243217	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151456	TAAAGCACTGGACCC[A/G]TGATGTGGCTGTTCT	114804
rs551244445	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144586	TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC	114804
rs551255338	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76186245	GTGCGGTGACTCATG[C/T]CTGTAATCCCAGCAC	114804
rs551284687	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76171635	ACAAAACAAAGAACA[A/C]CCTTCAAGTTAACAT	114804
rs551302050	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76225900	CAGTGAGAGCCTCCT[A/G]CTCCGCCCTCTTCTT	114804
rs551320949	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76228119	AAAAAACCATTTATG[A/G]AATATTCCATTTCCC	114804
rs551348453	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76193326	TAGTGATAACATCTT[C/T]ATTAAAGAACTTGTA	114804
rs551385239	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76186678	GGGGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA	114804
rs551424047	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76187308	CCTGCCTCAGTCTCC[C/T]GAGTAGCTGGGATTA	114804
rs551470870	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150493	CAACTCCCAGCAGCT[A/C]CCTCTGCCAAAAAAA	114804
rs551502447	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76210457	TAGCCGGGTGTAGTG[A/G]CGGGTGCCTGTAGTC	114804
rs551523646	in-del	-/A			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153873	GACCAGCTGCCAAAT[-/A]GTCCTCCCCCTCCCC	114804
rs551523756	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76227386	TCAGCTTCCCAAACT[A/G]CTGGGATTACAGGCG	114804
rs551528777	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76220633	AGGCAACATGGCAAG[A/G]CACTGTCTCTACAAA	114804
rs551615757	snp	A/G	0.00438332	0.0466095	intron-variant	RNF157	GRCh38.p7	17:76181718	TTTGAGACCAGGCTG[A/G]CCAACATGGTGAAAC	114804
rs551622287	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76188556	GTTCCAACTTTAAAC[A/G]AGGTGCAAGCAAAGA	114804
rs551658518	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76222236	CTGTGATCCCAGCTA[C/T]TTGGGAGGCTGAGGC	114804
rs551698090	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212988	ATAGCAGGGAAAACC[C/T]CAGATACCAAACGTA	114804
rs551737422	snp	A/C	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76190238	GTGGCACAATTTCGC[A/C]TCACTGCGACTTCCA	114804
rs551762081	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76222200	AAAATACAAAAATGA[G/T]CTGGGTGTAGTGGCA	114804
rs551776121	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76183086	ATTACAGGCGTCTGC[C/T]ACCATGCCTGGCTAA	114804
rs551820225	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76207366	AGTTTGAGGCTGCAG[G/T]GAGCAATGATCACGC	114804
rs551844341	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76233412	TTTATTATTATTTTT[C/T]ACTTGTATGGATTTT	114804
rs551845065	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76148786	GCATTGCCCAGGCTG[A/G]TCTCCAGCTCCTGGG	114804
rs551856933	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76227372	GTGATCCGCCCACCT[C/T]AGCTTCCCAAACTGC	114804
rs551981132	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76171903	CTATGACCTCACAGC[A/G]GCTCAGGCCCTTGAA	114804
rs551993617	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76225024	CAAAAACACAAAAAT[C/T]AGCCGGGTATGGTGG	114804
rs551998824	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76173988	GAAAACTGGGATGCA[A/G]TTTGGGGCCCAAAGA	114804
rs552035277	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76210375	AAGGTGGGCGGATCA[C/T]GAGGTCAGATCGAGA	114804
rs552072454	snp	A/G	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76168453	TTTTCTTCCAGTTGC[A/G]TAGTTTCCTATGTAC	114804
rs552087234	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76177900	GGATGACCTTCCTGC[A/G]GAAAAGAGCTTCCCA	114804
rs552096168	snp	C/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76210416	TAACACAGTGAAACC[C/G]CGTCTCTACTAAAAA	114804
rs552109593	snp	C/G	1.64806e-05	0.00287054	intron-variant	RNF157	GRCh38.p7	17:76161524	GGGCCGTGGTTCCGA[C/G]CCCAACTTACTGGAT	114804
rs552158506	snp	A/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145525	ACGGAGAGAAGCAGG[A/T]GCTGACAGGTGCAGA	114804
rs552222814	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76170435	GGCTTTACCATATTG[C/T]CCAGGCTGGTTAGCC	114804
rs552224815	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76163173	TGCAGCAAAATTACA[C/T]CTCTTGGCCCTGTTT	114804
rs552245967	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76224254	TTTTGGGACATATTC[C/T]TAATACCACAGTGAA	114804
rs552261921	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76163814	CATGAGGCAACTCAC[C/G]AAGGCCTGGCCTGCC	114804
rs552320453	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76176736	GCGGTAGGGCAAAGA[A/G]GAGCCCCGAGGCGGA	114804
rs552467891	snp	A/G			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212557	AAAAAAAAAAAGCTG[A/G]TTTTTAAAATGTTAA	114804
rs552473728	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76165866	TATTTTTAGTAGAGA[C/T]GGGGTTTCACTATGT	114804
rs552508367	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76166392	GTTGTTCTGGGGCCA[C/G]AGCTGCTGCCAGGAA	114804
rs552548326	snp	A/G	8.61542e-05	0.00656275	intron-variant	RNF157	GRCh38.p7	17:76166579	ACTTAACACATTTAC[A/G]TGGCACAGCTAATCT	114804
rs552550144	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76158669	TCCTGGGCTTCAGCG[A/G]TCCTCTTGTTGACGC	114804
rs552578368	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76157661	CTGAGCAACAACAAC[A/G]TGCCAGGCACATGCT	114804
rs552587074	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76159232	GGAACAGCCCAGAGG[G/T]TTACTCTGCCCTAAG	114804
rs552612712	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152732	AGGAGGGCTGTGGGA[C/T]ACAGGCTCAACAGAG	114804
rs552641325	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76195845	GCTAAAACAGGGACT[A/G]GGCAGAAGCAGCTTT	114804
rs552684863	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76208697	AAAAACATTTGCCAG[C/T]GCGGTGGCTCACACC	114804
rs552707970	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76201966	GAGATTCGGAGAGGT[C/G]AAACAGTTGGGCCAA	114804
rs552716704	snp	C/T	0.00398564	0.0444627	intron-variant	RNF157	GRCh38.p7	17:76185421	CAGACACAGTCATCT[C/T]TTCCCCTCCAGCGAG	114804
rs552774927	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76215949	GCCCTATTTTCCAAG[C/T]GCATAATTTATGGAG	114804
rs552784538	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76198078	CACCTTCCTTTCTGG[C/T]CACCCAACCATAATT	114804
rs552814695	snp	G/T	0.00159617	0.0282053	intron-variant, missense	RNF157, RNF157-AS1	GRCh38.p7	17:76152219	TTCCTTCAGCAACTG[G/T]TCTCCAGCACTAGCA	114804
rs552823178	snp	A/C	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76192136	ACACTTGGTTTCAAT[A/C]TGTTTCAAAGAAATT	114804
rs552865115	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76190779	GGGCATGGTGGCAGG[C/T]GCCCTGTAGTCCCAG	114804
rs552927847	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76236808	AAAAGCACAAAGAAA[A/C]TTATCAAATATGAGA	114804
rs552952113	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76226633	AGTCAGCCATTCGGA[A/G]GAGCCCGCCTTAGCC	114804
rs552990657	in-del	-/A/AAAAAAAAAGAAAAGA	0.00146806	0.0270531	intron-variant	RNF157	GRCh38.p7	17:76166550	AAAGAAAAGGAAAGG[-/A/AAAAAAAAAGAAAAGA]AAAAAAAAAGAGGAC	114804
rs552998535	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76230562	AGGAGATACTGAGCC[G/T]GGCATGGTGGCTCAC	114804
rs553034713	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76154795	GGTCAGGGCACGTCT[C/T]ACACTGAACTGTGGT	114804
rs553075374	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76238745	AAGTTTTCCTCATGC[C/T]GCCCTAAGAATATTT	114804
rs553175447	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76175463	TTGCCCTCCTGCAAG[C/T]AGTGCATCAGGAGGC	114804
rs553189623	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76232078	CATGTATCAGTAGTT[C/T]ATCCCTTTAAATTGT	114804
rs553257526	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76226970	CTGCAAAGGCCAATG[C/T]TGCCGCAGGCACTGC	114804
rs553267782	in-del	-/T	0.141596	0.225274	intron-variant	RNF157	GRCh38.p7	17:76163191	CTTGGCCCTGTTTCC[-/T]TTTTTTTTTTTTTTT	114804
rs553268870	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76178194	AGAGCTGTGGCCCGT[C/T]GGGGAGCCCAGACCT	114804
rs553326208	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76217208	AGAGATGGAGTTTCA[A/C]CATGTTGGCCAGGCT	114804
rs553369097	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76190543	GGGAAGTCAAAGCTG[C/T]AGTGAGCCATGATCA	114804
rs553391299	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76225920	GCCCTCTTCTTCTGG[C/T]GGTACCTAGTGGCTG	114804
rs553394440	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76224609	TTTTAAGTTTTCCCC[A/C]TAGAGCAAGGGTGCC	114804
rs553397271	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76234728	TCTTTTTATTATTGA[A/G]CATATGAGTTCCTTA	114804
rs553399138	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76227653	GAGGCCGAGGTGGGC[A/G]GATCACCTGAGGTCG	114804
rs553407731	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76183474	TGTTTTGTTTTTTAG[A/G]GGTAGGGTCTTGCTA	114804
rs553408780	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146575	TGGGCCTCCCCAGCC[A/G]TGTCTCCCAGTGGCC	114804
rs553472013	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76177654	CCTTTTCTAGGCCTG[C/G]CCATGGATGCCCAGG	114804
rs553484224	snp	A/G			intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153782	TGTCTCCTTGACCAC[A/G]CCTTTAGTACGTCTG	114804
rs553547528	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76221298	GACAGCAAATACAAC[A/C]AAGTAGTCTTACCAA	114804
rs553563718	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144116	ACAGGGACAAGAATG[C/T]CACCTCCCAATTGAG	114804
rs553625127	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76217900	TCTCCAAGATTATAC[A/G]TAAACCGTAAGGTAT	114804
rs553700918	snp	A/C	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76210395	TCAGATCGAGACCAT[A/C]CTGGCTAACACAGTG	114804
rs553711600	snp	A/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76210490	AGCTACTCAGGAGGC[A/T]GAGGCAGGAGAATGG	114804
rs553719385	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76204260	TCTGCCTCAGATGCC[G/T]CTCCTCATCTCCCCT	114804
rs553734247	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76170037	GGACTTGGGGATCCT[G/T]GGCTTCACTGTGGGC	114804
rs553769987	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76143364	GTAACACCACACTGT[G/T]AATACTACCTGCAGG	114804
rs553770730	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76187786	AATTTTTAGTAGAGA[C/T]AGGGTTTTACCATGT	114804
rs553847365	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76211804	ATGCAGAGAAGGTGC[A/G]CAATAGAAATTTATG	114804
rs553854143	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76221828	TACAACGGAATATTA[C/T]TCAGCCATAAAAAGA	114804
rs553908673	snp	A/G	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76175633	AAATCCGACACAAAC[A/G]CTAGTCTATTCTAAA	114804
rs553918046	snp	G/T			missense, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156293	GACGACAAGGTGAGA[G/T]TCTCACTTTCTGGAG	114804
rs553946673	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76181538	ATACGTCAGTCAGCG[A/T]TTACCTTCCACCCAA	114804
rs553947150	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76169568	TGAGCCACCACACCC[A/G]GCCTAGTTAGGTTTT	114804
rs553982486	snp	C/T	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76227103	GCCAAATAATATTAA[C/T]AACCTCTTTTTTTGT	114804
rs554094005	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76179467	GAGGTCGAGGTGGGC[A/G]GATCACTTGAGGTCA	114804
rs554094049	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76209756	AAGAAACGGCTACTT[A/T]CATTTTTGTTTTTGT	114804
rs554107378	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76208259	TATTTCAGAAATTGC[A/C]CTTGAAGATCTACAC	114804
rs554111987	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB	RNF157	GRCh38.p7	17:76240689	GGCGGGGGCGTGGGC[A/G]TGGGCGGGGACTCGC	114804
rs554119670	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76208738	GCACTTTGGGAGGCC[A/G]AGATGGGCAGATCAC	114804
rs554124807	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76177478	GCCAGCCCCCTGCTG[C/T]CTCGGCCCCTTCCAG	114804
rs554151970	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76174055	ATTTCGGTCAGTGTT[C/T]AAAACCTGGAGAATT	114804
rs554172423	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76220299	ACTTAAAGAGGTTCC[C/T]GCAGAGCAAAGATGG	114804
rs554209169	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76198920	TGCAGTGCACACACC[A/G]TCTGTTGGTGAGATG	114804
rs554285738	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76171431	TGACCTCGGTGATCC[G/T]CCCGCCTTGGTCTCC	114804
rs554359213	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76167191	GGGTCTGACAACTTC[C/G]TCTGCTCATGCCTGT	114804
rs554368353	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76233198	GTGCTGGGATTACAG[A/G]CGTGAGCCACCGTGC	114804
rs554395708	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76160824	ACTAAATAATCATCT[A/G]TAATTTATTCTAGAT	114804
rs554425034	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76239350	TACCACAATCCAGAG[A/G]CTAGAGACATTTAAG	114804
rs554432329	snp	A/G	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76161606	GGGACAAGGGGCCCA[A/G]TTTTTTCCTCATGGC	114804
rs554436124	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76199975	GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	114804
rs554474873	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194054	CCAAGGCACATTCTG[C/T]TTTTTTGTTGGTTTG	114804
rs554480033	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76219881	ATTAAGCAGATGAGT[A/G]ATTATGTGATTTTCA	114804
rs554480493	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76196533	TATTTTTAAAGAGGA[C/T]AAGTCAGCCCTAGGT	114804
rs554495655	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76200523	GAGTAGTCAAACTCA[C/T]AGAGGCAGAAAACAG	114804
rs554533480	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76228885	GCTGAGACTGCGCCA[C/T]TGGACTCCAGCCTGG	114804
rs554566745	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76164533	CTCAAAAATCAGCAT[G/T]CCTTTCAGGCCACCC	114804
rs554578792	snp	A/G	0.00636936	0.0560724	intron-variant	RNF157	GRCh38.p7	17:76157112	GCTGGGACTACAGGT[A/G]CATGCCACCACACCT	114804
rs554594639	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76191557	AGTGAGCTGAGATCA[C/T]GCCACTGCACTCCAG	114804
rs554657028	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76163383	ATTTTGTGGTAGAGA[C/T]GGGGTTTCACCATGT	114804
rs554726416	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76222450	GATAATTTTATGTTA[C/T]GTGAACTTCGCCTCA	114804
rs554743938	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76182828	ATATATCCTATATAT[C/G]CTATATATGATATAT	114804
rs554792376	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76195044	AAACACAAGAGCAGA[A/G]GGAATGGGAGAGGAT	114804
rs554794795	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76158187	CCCAGCTACTATCCT[C/T]AGCATATAGCACAGT	114804
rs554827092	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76189745	AGATCCTGGAAGCCC[A/G]GAGAAGGGACCCTCC	114804
rs554831520	snp	A/C	1.66421e-05	0.00288458	intron-variant	RNF157	GRCh38.p7	17:76158534	AAAAGCAGCTATATC[A/C]AACGTCCATTTAAAG	114804
rs554887125	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76176932	AGGTTCCTGTGCCTC[A/G]GGAGGAGGTTCTGCG	114804
rs554914546	snp	A/G	9.33036e-05	0.00682958	synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145328	GGCATTCCGACTGAC[A/G]GCATTGTCATCAGCC	114804
rs554938534	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154447	CTACGTTAATAGCAT[A/G]TATTTCCATCTGTGT	114804
rs554978109	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76154853	AGATGGGTGCAGTGG[A/G]CTGGGGGTAGGCAGA	114804
rs555015409	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76148305	GGTCTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG	114804
rs555037460	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194886	CAGGCGTGGTGGCGG[A/G]CGCCTGTAGTCCCAG	114804
rs555053434	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149095	AACACACTACTCCCC[A/C]GTGAAAAACCAAAAA	114804
rs555054524	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76144978	TCCACCTGAACATCA[A/G]TATACCGTGAGGACA	114804
rs555070813	snp	A/C	0.00636936	0.0560724	intron-variant	RNF157	GRCh38.p7	17:76189060	GAAGAACAAGGAAAA[A/C]TTGAGAAACTAGCAC	114804
rs555116059	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76229094	ACCAAACCAAGTCTT[A/G]TCTCACACTTCATTT	114804
rs555126743	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76179418	AAAAAGAGGCCAAGC[A/G]TGGTGGTTCATGTCT	114804
rs555145488	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76179999	TGACAAGGAAGACCA[C/G]ATAAAGTCTTTCTGA	114804
rs555165221	in-del	-/A	0.234982	0.249549	intron-variant	RNF157	GRCh38.p7	17:76238086	GAGAGACGATGACTC[-/A]AAAAAAAAAAAAAAA	114804
rs555212314	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76191677	TCCTAGGAAGGCTGA[C/T]GTGGGAGGACTGCTT	114804
rs555219092	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76186368	AAAAATTAGCTGGGC[G/T]TGGTGGCGGGTGCCT	114804
rs555395889	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76240055	TCCGCAACCACTGAG[G/T]CCCCGAAGACCCGCG	114804
rs555431757	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76225978	GCTTCTTATCCAGTT[C/T]CTCACCCTTTACTTT	114804
rs555439773	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76184523	TTGAATGCTGTGAAG[C/T]GAATACAAATTTGCC	114804
rs555457678	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76235893	ATGTGCCTGTAATCC[C/T]AGCTACTGAGGAGGC	114804
rs555503428	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76186935	ACAGAATGAGACTCC[A/G]ACTCAAAATAAATAA	114804
rs555554843	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76221510	GAATATATTGTAAGG[C/G]GGGAAAGTATGGCAA	114804
rs555557114	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76177876	CTGCTGAGAGCTGCA[C/G]AGAAGACAGGATGAC	114804
rs555566476	in-del	-/A	0.17332	0.23795	intron-variant	RNF157	GRCh38.p7	17:76181908	GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	114804
rs555575255	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150368	CTCTCTTCCTCCCAG[C/T]CCTCACTCTCCTCCC	114804
rs555689468	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76220344	CATCAGGATAATAAG[A/G]GCAAGGAATAAGTCT	114804
rs555698722	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76166622	TACTGTCAAGAAGCA[G/T]TAATCTCATCTCTGC	114804
rs555745337	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76229742	GAGCTACTTAGAATG[A/G]AGAGTGGCACACTAA	114804
rs555820701	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76217339	AAGGAAAAATAAATT[C/T]ACTTATTGGTATTTC	114804
rs555865592	snp	A/C	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76192044	CCAGATTTTTCTTTG[A/C]AATGCAAAACCAGTA	114804
rs555871963	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76188747	AATTAAGTGGGAAGT[A/C]AAAAGTTCAGCAAGA	114804
rs555917018	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76228940	AAATAATAATAATAA[C/T]ACAAAAAAAAAAATT	114804
rs555938783	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76172288	CACTGTACTGCAGCC[A/T]GGGTGACAAAGTGAG	114804
rs555939059	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76178697	TATCTTATTTAATCT[C/T]TGGAGGAATCCTGTG	114804
rs555976296	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213903	TTCTGGAGGGTAACA[C/T]GCCCAGAGACGGCAT	114804
rs555977798	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76173014	AAAGAAGGCTGGGCG[C/T]GGTGGCTCACGCCTG	114804
rs556069527	snp	C/G	1.66674e-05	0.00288676	intron-variant	RNF157	GRCh38.p7	17:76159577	ATTCTCTGAGGACTA[C/G]GGGAATCAGAGACAG	114804
rs556117480	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76174540	ATTTCAAATGTTCCC[A/G]GTATTTTTAAAATGT	114804
rs556132941	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76205828	GAAACTGTGTCAATG[C/T]GGCCCAGCTACAGAA	114804
rs556139676	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76164218	CTGGCACATGGTAGG[A/G]GCTGGGACTTTCTAG	114804
rs556142736	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76188467	CAGGGCTTGTCAGAG[G/T]TGATTACACTCCCTG	114804
rs556148304	snp	A/G			intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76154878	GGCAGAAACCTCACC[A/G]CACAGGTCTGTATAG	114804
rs556162159	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76209547	TCCGTGTGTGGCCCA[A/G]TGTGACAATTCTTCT	114804
rs556265625	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76194738	CCACAAGAGCAGGCC[A/G]GGCACGGTGGCTCAC	114804
rs556273222	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76200036	AGGTCAGGAGATCGA[A/G]ACCATCCTGGCTAAC	114804
rs556350792	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194759	GGTGGCTCACACCTG[A/T]AATCCCAGCACTTTG	114804
rs556355779	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76163421	GCTGGTCTCAAACTC[C/T]TGACCTCAAGTGATC	114804
rs556389482	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76170070	ACCTGGATCTGTTGA[A/G]GAACCTCTAACTCTA	114804
rs556410142	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76170750	TTCTTTCTGCTAGTT[C/T]AGGATTCTGATTTCC	114804
rs556471872	snp	G/T	0.000319965	0.0126444	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76162563	TTACCTTAGAATCTT[G/T]TGTGTTGTACTTGTT	114804
rs556473841	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76196687	CTGTACCCCTGCTGT[A/G]GAGAGTTTTGGCTAC	114804
rs556484819	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212660	TGAGATAAGGAGTTC[A/G]AGACCAGCCTGGCCA	114804
rs556485144	in-del	-/TCTT			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153111	TTTATCAAGCTCCCC[-/TCTT]TTTTTCTCAGTGAAA	114804
rs556492082	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76187838	CCTGACCTCAAATGA[C/T]CTGCCTGCCTTAGCC	114804
rs556493804	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76201714	CTCTACATTATACAC[G/T]GCAACTTGCTTTATT	114804
rs556509551	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76171661	AACATTTATTGAACA[C/T]CAGGTGTTTTCCCTT	114804
rs556518937	snp	A/C	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76234040	GCCTCTGGCAGCCGC[A/C]GGCACAGCCACTGCG	114804
rs556530643	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194910	GTCCCAGCTACTCAG[G/T]AGGCTGAGGCAGCAG	114804
rs556536133	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76172077	CTGCAGCAGACAGGT[A/G]CCTCCTTGAATCTCT	114804
rs556539619	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76168668	CTGGTGGGTCCCTTT[C/T]GCCTCTGTCCTCCTG	114804
rs556546486	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB, downstream-variant-500B	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142132	TCCTCCTCCCTTCCC[C/T]TGGCCTCCCTCCTGT	114804
rs556570900	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76166045	AGTGGCACAATCTCG[A/G]CTCACTGCAACCTCC	114804
rs556576371	snp	C/T	1.66579e-05	0.00288595	intron-variant	RNF157	GRCh38.p7	17:76161671	GAGAAAACAGGCAAT[C/T]AGGACATCCTGATAC	114804
rs556623558	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76163449	ATCCACCTGCCTCAG[C/G]CTCCCGAACTGCTAG	114804
rs556650944	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76210391	GAGGTCAGATCGAGA[C/T]CATCCTGGCTAACAC	114804
rs556733836	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76210095	AAGCTGACTCCCTGT[A/G]AGTGAGGCAACATTT	114804
rs556745530	snp	A/C	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76192075	AGTATAGTTTCCCGT[A/C]AGATGGGGTGCACAA	114804
rs556785851	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153704	TGAATTATGGTAAAG[A/G]AAGATTATTACAACA	114804
rs556789822	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF157	GRCh38.p7	17:76156015	GCTGAGAGAATTAAC[A/G]CCCCACTAGCTACAG	114804
rs556828227	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149990	GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGG	114804
rs556828574	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76156508	AAGCCTGGAATGACT[A/G]CCTCCCAGGGGAGGC	114804
rs556834503	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241991	ATGGTGGGAACACAT[C/T]CCTGTCATTTATATT	114804
rs556859577	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76170961	GCAGTGGCACAATCT[C/T]GCCTCACTGCAACCT	114804
rs556935328	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76232000	AACTCATACGATATA[C/T]AGTCTTGCATCTAGT	114804
rs557005327	snp	C/T	0.00438332	0.0466095	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145428	CTCCAGCAGGGCAGC[C/T]CAGGAGCCGGCACGG	114804
rs557026615	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76159162	CTTAAGTACCTACAT[A/G]CCATCTTATTTTCAT	114804
rs557182055	in-del	-/A	0.0599851	0.162463	intron-variant	RNF157	GRCh38.p7	17:76190603	GTGAGACCCCATCTC[-/A]AAAAAAAAAAAAAAG	114804
rs557189117	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76171451	CCTTGGTCTCCCAAA[A/G]TGCTGGGATTACATG	114804
rs557210168	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76225777	TTTTCTTCCCCCTTG[C/T]CTTGCGGACCTCTTC	114804
rs557237930	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76232356	TCGCACCACTGCACT[C/T]CAGCCTGAGCACTTA	114804
rs557259674	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76183270	GAAAACTGCAGATCC[C/T]AGGGCCCTGTCACTA	114804
rs557273598	snp	A/G	0.00438332	0.0466095	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147503	CTTGCTACAAACTCC[A/G]ACCTTCTATTCTATA	114804
rs557292348	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76177543	GGGGGAGAGGCGAGG[A/G]GGTGCTGAGGGCAGC	114804
rs557317893	snp	A/C	0.000289394	0.0120255	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76240156	GCCCGCCCTCACCGG[A/C]CTTGGGCGGGTAGCG	114804
rs557365585	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76195142	GGGCCGAAATCCCAA[A/G]TGGCAGAAACATATT	114804
rs557366102	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76236091	GATTATGTGGGTGGG[C/T]CTCTAGTCAGTTGAA	114804
rs557373053	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149240	GAACCAACAAGGTTC[A/G]CAGTCCTTGCCACCA	114804
rs557379197	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241116	CCTCCCTCTCACGTG[C/T]GTCTATTCAAAGCGC	114804
rs557478998	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76182836	TATATATCCTATATA[G/T]GATATATAGGATATA	114804
rs557513264	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76233174	ACCCACCTGCCTCAG[C/T]CTCCCAAAGTGCTGG	114804
rs557525425	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76227142	TTTTTTGAGACGGGA[A/G]TCTCACTCTTGTCGC	114804
rs557615251	in-del	-/C	0.0115144	0.0749975	intron-variant	RNF157	GRCh38.p7	17:76237004	GTGGATGGACAACAG[-/C]GGTGAGAACAAGGCT	114804
rs557616793	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76180137	CTTACCTCAAGCTCA[A/G]TATGGATTTATAGAA	114804
rs557638157	snp	C/T	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76210273	CTACTGGACGAAAAA[C/T]TAGCAGAGGGGTCAC	114804
rs557674326	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76152145	CTATCCTAATACTCT[C/T]ACTCAGAGCAAGGCT	114804
rs557681121	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76225302	CCAGCCTGGGCAACA[C/T]AGCAAGACTCCATCT	114804
rs557762823	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76221788	TAAACAAAATGTGAG[A/G]TATAATGTGTCCGAC	114804
rs557795707	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76187059	AGTTTATAAGCCAAA[A/C]AAACATGGAATTCAA	114804
rs557955508	in-del	-/T	0.0414363	0.137845	intron-variant	RNF157	GRCh38.p7	17:76220655	TCTACAAATTTATTA[-/T]TTTTTTTTTTTTTAG	114804
rs557956847	snp	C/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76174759	TTGGGAAACAATATA[C/G]TTAAACCATAGTTAA	114804
rs558015250	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76221090	TGCACCACTGCACTC[C/T]AGCCTGGGCAACAGA	114804
rs558026193	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76206002	TCAGAGGCCAAGACA[A/G]GAAGACTACTTGAGC	114804
rs558075042	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76232990	CAGTGGCCCAGTCTC[C/T]GCTCACTGCAACCTC	114804
rs558078603	snp	A/G	0	0	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212708	CTCTACTAAAAATGT[A/G]AAAATTAGCCGGGTG	114804
rs558090822	in-del	-/TC	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76179431	GCGTGGTGGTTCATG[-/TC]TCTAATCCCAGCACT	114804
rs558090869	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213512	GAGGCAGAGGTTGCA[A/G]TAAGCCAAGATCACA	114804
rs558102196	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76179216	CCTGGGCAACATGGC[A/G]AGACTTTGTCCCCAC	114804
rs558134435	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76154959	GTAAATACTAGTGGA[A/G]TGAAGGACAATATAT	114804
rs558162833	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76214749	AGCCAGGAGGCAGAA[A/G]TATTTTCAGTGCAAT	114804
rs558207252	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76173026	GCGCGGTGGCTCACG[C/T]CTGTAATCCCAGCAC	114804
rs558226249	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76215347	GGGCATGGTAGCATG[C/T]GTCTGGAGTTCTAGC	114804
rs558240085	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76173499	CACAAACACAGACGA[C/T]TGCATCCAGTGCTGA	114804
rs558290546	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76229763	GGCACACTAAGGGTA[C/T]GTATGGGTGCTTCTG	114804
rs558299822	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76210061	CCGTGCCCAGCAGAA[A/G]GGGCTACTTTCAAAG	114804
rs558421980	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76206633	TAGTGAAACCCTGTC[C/T]CTACTAAAAATACAA	114804
rs558427720	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76193648	GACACTGTCTAAGGT[A/G]ACGTGAGAGTTAAGC	114804
rs558510460	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76176338	TTGGTAGTTGATCTG[C/G]GATCCTAAAGGATAA	114804
rs558566779	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76203260	TCTCCCAAAATGCTG[C/T]GACTACAGGCGTCAG	114804
rs558577460	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153116	CAAGCTCCCCTCTTT[A/T]TTTCTCAGTGAAACA	114804
rs558609302	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76196239	ACCATGAGATAAATA[A/C]ATGTCACAAAGATGC	114804
rs558609583	snp	G/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76170214	GGGCTCAACATCCAG[G/T]ATGCCAGGATCCACT	114804
rs558693216	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76188256	CTGCATCCCACGGCC[C/T]CCTACCTGGGATCAC	114804
rs558734159	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76188860	TAAACAGGGCTGATA[C/T]CAACAGCAATAAGTC	114804
rs558779945	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152554	TCTTAAGGATGGAGA[C/T]AAAAAAAATCAAATC	114804
rs558783805	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76164319	AGGAATGGATAAATT[A/C]AGCCAATGACTCTAA	114804
rs558815364	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76201314	AACATAGTGAGACCC[C/T]AGTCTCTACAAAAAA	114804
rs558817508	in-del	-/TT	0.331642	0.236293	intron-variant	RNF157	GRCh38.p7	17:76169580	CCCGGCCTAGTTAGG[-/TT]TTTTTTTTTTTTTTT	114804
rs558822348	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76165358	GGTGGTGCCATCTCA[A/G]CTCACTGCAACCTCT	114804
rs558824253	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76157408	GCTTGCTCCGAGCCC[C/T]GACTTCCTGCTCTGT	114804
rs558865181	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76158119	GTCTTTTGTGCCCCC[A/C]ACCCCAGATAGCAAG	114804
rs558868557	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76182065	AGTTCCATCTGTAAA[A/G]GGGCGTCAAGCTTGC	114804
rs558874466	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76190857	AGCTTGCAGTGAGCC[A/G]AGATCGTGCCACTGC	114804
rs558930746	in-del	-/GGAG	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76168561	ATTTCATCTTATTGA[-/GGAG]GGAGGTCCCTTGGAC	114804
rs558962181	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76208150	CTGGTTTTCAATTTC[A/T]AGGCTCAAGAGATCT	114804
rs558974867	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76156666	ATGATCAGCTTTCCT[A/T]CTGCGGCAAAAGCAT	114804
rs558975077	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76202073	GAAGGAAGAAGGAAA[C/G]AAGATAGCATGCAAA	114804
rs559003162	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76200622	AGTTTTGTGAGATGA[A/G]AGGAGTTCTGGAGAC	114804
rs559012242	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76184023	GGTGAAACCCCGTCT[C/T]TACTAAAAACACAAA	114804
rs559054158	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76184959	TTAATTAAGCAATTG[C/T]ACAGTTAAGCAATTC	114804
rs559064900	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76242099	GCAGAGTCCCTGGTC[C/T]TAACTACTCCAGGGC	114804
rs559084707	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76178409	ACAGCGGCAGCTGGC[A/G]TGTCTGACTGCACAG	114804
rs559085689	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153301	ACACTCCAAACCCCC[C/T]TGGGCTGGGGTGCAA	114804
rs559137512	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76230765	ATCGCTTGAACCCAG[A/G]AGACGGAGGTTGCAA	114804
rs559185092	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76210418	ACACAGTGAAACCCC[C/G]TCTCTACTAAAAATA	114804
rs559202340	snp	A/T			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213054	TGAATTCTTCTAATG[A/T]TCTGTTTAAAATACC	114804
rs559233347	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144338	TCTTTTTTTTTTTTT[C/T]TCTCTGTCGCCCAGG	114804
rs559246788	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76210554	AAGATCGTGCCACTG[C/T]ACTCCAGCCTGGGCG	114804
rs559256211	in-del	-/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76235294	GCTCCGCCTCCTGGG[-/T]TCACATCATTCTCCT	114804
rs559307981	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76230230	CTGTGGTTTTGGGAA[A/G]TAAGTGGGTTTCTGT	114804
rs559363575	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146877	TCACAAGTGTCCAGG[G/T]TCAGCCTCAGGCCAG	114804
rs559391733	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76191678	CCTAGGAAGGCTGAC[A/G]TGGGAGGACTGCTTG	114804
rs559431926	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76230931	TTAGATTAAAAGATT[A/T]AATCTTTTTTTTTTT	114804
rs559450669	snp	C/T	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76210506	GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAGGC	114804
rs559462730	snp	C/T	0.00318978	0.0398085	intron-variant	RNF157	GRCh38.p7	17:76231447	GTCTTTTGAGGCCCA[C/T]CACCATGCCTGGCTA	114804
rs559474489	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76168190	TATACTTGGGTTACT[A/T]CTTCTTGATTTTTCA	114804
rs559490649	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76177146	CCCGGCCCTGGCCCC[A/G]GCCCAGTGAGGACCT	114804
rs559512199	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76211335	CAGTTCAACTCCCTG[C/T]ACCTCTTCCCAGTGT	114804
rs559535117	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76157765	TGCCCTGCTGTATCT[A/C]GCTCAGTGCCCTACA	114804
rs559535172	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76165627	CCAGTTCCCTGCAAT[A/C]TGGCAAACCAAATGT	114804
rs559538450	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76231936	AGGCAAACACTATTC[C/T]GCTTTCTATCTCTAT	114804
rs559546871	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76226193	TCCTTTATGCACTGA[A/G]GGATCATGGCAACGT	114804
rs559561383	snp	C/T	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76218298	AGTAACATTCTAAGG[C/T]AGTCAAAGAAAGAAA	114804
rs559570453	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76158325	GCAGAGGGACCTGAT[A/G]AGGCATGCAGGTAGG	114804
rs559594177	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76217489	ACTTGCTCAGTCTTT[C/T]TAGAGGGACAAATTG	114804
rs559598327	in-del	-/A	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76226114	GGGGCTATGCTGAGG[-/A]GACCCCAGATAGGAC	114804
rs559631357	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76171114	AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT	114804
rs559636986	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76173114	ACATGGTGAAACCCC[A/G]TCTCTATTAAAAATA	114804
rs559663466	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76176743	GGCAAAGAGGAGCCC[C/T]GAGGCGGAGCTGGGC	114804
rs559723197	snp	A/C	1.64849e-05	0.00287092	intron-variant	RNF157	GRCh38.p7	17:76166415	GCCAGGAATATGCCA[A/C]AAAAGAGCAGTGTGC	114804
rs559750505	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76182890	CATAATAATATGAAA[A/G]CTATATTATTACCAT	114804
rs559774032	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76173531	CAACATGGGTGTGGA[C/T]GGCCTGATCTCAGCA	114804
rs559821672	snp	C/T	0	0	intron-variant	RNF157	GRCh38.p7	17:76216649	AGTATTATGAAGCCT[C/T]TCAAAGTGGTGTTGT	114804
rs559845835	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76215662	TAAAACTTTCTACAC[A/G]AGGAGCTTTAGTCTA	114804
rs559875339	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76171677	CAGGTGTTTTCCCTT[C/T]TGTTACCTTAATTTT	114804
rs559894476	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76161454	TTCCTTGCTGCAATG[C/G]CACGTAGAGAAGCAT	114804
rs559909786	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76209862	CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA	114804
rs559937445	snp	C/T	0.000143554	0.00847093	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155655	GATGTAGGAGCCAGA[C/T]ATGGAGGAGACGGTG	114804
rs560014570	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212780	GGCAGGAGGATGGCT[C/T]GAACCCAGGAAACAG	114804
rs560048698	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76220819	AAAAATTAGCTGGGT[A/G]TGGTAGTGTGCACCT	114804
rs560080091	in-del	-/TGTTCCC	0.00398564	0.0444627	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153562	TCCTGGAACACATAG[-/TGTTCCC]TGCTTGGGGGAGACT	114804
rs560152646	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76205326	TTTTGTAGAGTCGGG[A/G]TTTTGCTATGTTGCC	114804
rs560158870	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76180263	TTTTTATAATGAAAA[C/T]AGGCCTCAGATCAAG	114804
rs560180380	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76211956	AGGTTTGGGATACTA[C/T]AGTAAAAACAGTCCT	114804
rs560235033	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76168329	ATGATTTTATTATAA[C/T]AGTCCAGTACATTTG	114804
rs560269027	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76165687	TATAACCCATACTTT[C/T]TTTTTTTTGAGACAG	114804
rs560328151	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76205306	ACCACCCCTGGCTAA[C/T]TTTTTTTTGTAGAGT	114804
rs560339336	snp	A/G			intron-variant, nc-transcript-variant	RNF157	GRCh38.p7	17:76156461	TGGCATGCAGAGGCC[A/G]CAGCTTCTCTCTTCC	114804
rs560358706	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76198294	AGGGACATTCTCTTA[C/T]GACACAGAATGAACA	114804
rs560363039	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241582	GCTATTTTACGGAGT[C/T]TAGGTCTTTCCTGGT	114804
rs560367538	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76233212	GGCGTGAGCCACCGT[A/G]CCTGGCCTCTTGCAC	114804
rs560367621	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76226875	TCGGTTACAGCAATG[C/T]TGCTGCTGAATGCCG	114804
rs560378582	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76208674	CCTAATATAAAATTA[C/T]GTCTTTTAAAAACAT	114804
rs560411886	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76194402	GACTTTCAAATACAT[C/T]AGAAATAGTGAAGCC	114804
rs560427164	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76227281	ACCTGCCACCACACT[C/T]AGCTAATTTTTGTAT	114804
rs560427226	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76207779	CTCAAGCTACATGTC[A/C]ATCTTCAATCTCTGA	114804
rs560435942	snp	A/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151629	TTGGAGCCCTTGAAC[A/G]GGCACACTAACTAAA	114804
rs560446898	snp	A/G/T			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146391	CCTCCAGGCCATCTC[A/G/T]CCTCTCCCCTGGGAG	114804
rs560494102	snp	C/G	1.68233e-05	0.00290023	intron-variant	RNF157	GRCh38.p7	17:76159609	TTGAAAAATTAATTA[C/G]GTCCTTTTTGTTTTA	114804
rs560517038	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147921	GTATGAAGAGACCTC[C/T]AGAGGTAGATTTTGG	114804
rs560530853	snp	A/C	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154627	TCTAAGGTGGAAGTA[A/C]AAATTACTAAATGAA	114804
rs560650528	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76202416	CACTGCATTCATTTT[A/T]TTTTCTGTTTTTTAG	114804
rs560651066	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76198777	GTTCCCCACACCTAC[A/G]GGACAAAAATTCGAA	114804
rs560666301	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76155003	GGCTGGCCAGAAAAG[C/T]TCCCTCTTGAACTCA	114804
rs560686060	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76193213	TTTATAGCTTCTGTC[A/T]ATCTCATAGGGTCAT	114804
rs560699548	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76163671	TCGCTGATTTTATAT[C/T]CCACTCTCCGTTTTA	114804
rs560700030	in-del	-/T	0.00597247	0.0543191	intron-variant	RNF157	GRCh38.p7	17:76238893	CAATTCTTCACCATA[-/T]TTCATCTTTGCAAGG	114804
rs560726459	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76164859	CACCAGGTATTCTTC[G/T]GTTACATCTCCCAGT	114804
rs560754794	snp	C/T			intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76148327	GCTGGAGTGCAGTGG[C/T]GTGACCTCGGCTCAC	114804
rs560756004	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76186584	TTAATTACAAGAGTT[G/T]TCAAGATTTCTCTCA	114804
rs560775217	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76148427	ACTCGCCACCACGCC[A/T]GGCTAATTTTTTTGT	114804
rs560791350	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76230265	TTTCCCCGGATCTTG[A/T]GGCAAAGTAAAGCAA	114804
rs560792711	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76187156	TCACTATTCAATCAA[C/T]AACTCTAATAGGATT	114804
rs560800408	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76230710	AGGCATGGTGGCAGG[A/C]ACCTGCAATCCCAGC	114804
rs560810350	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, downstream-variant-500B	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142067	ATTAATTTCACCAAC[A/C]TTTAAGTCACAGGGA	114804
rs560826940	in-del	-/TTGGT	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76194062	CATTCTGTTTTTTTG[-/TTGGT]TTGTTTATCAAGGTA	114804
rs560851422	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76200206	AAGATCGCGCCACTC[C/T]ATGCCAGCCTGGGCG	114804
rs560879433	snp	A/G			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76148291	TTTTTTTGAGACAGG[A/G]TCTCTTGCTCTGTCG	114804
rs560918252	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76157444	TGCATGCATCGTCTT[C/T]TCCACATGGATGTTT	114804
rs561002265	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76235596	CTTTTATAGTTATTC[A/G]ACAAAGACTTATTAT	114804
rs561037301	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194951	ACCCGGGAGGTGGAG[C/T]TTACAGTGAGCCGAG	114804
rs561038107	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76181302	AAATCTCCAATGGCG[C/T]CCTATGCTTAGATGG	114804
rs561059235	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152599	AGACAATAATTAAGC[A/G]GATAAAGAGTGGACA	114804
rs561078419	snp	C/G	0.00438332	0.0466095	intron-variant	RNF157	GRCh38.p7	17:76194803	GGCAGATCACGAGGT[C/G]AGGAGATCGAGACCA	114804
rs561107857	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76242188	ACAGGCCCTACCTTG[C/T]AACTGCTGGGTAAAG	114804
rs561112619	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76175997	TAGGCTCTCCCTGTA[C/T]ACACACATACACGCA	114804
rs561114378	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76215426	GTTGCAGCGAGCTAT[A/G]ATTGCCACTGCACTC	114804
rs561133498	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145188	CAGCTGAGTGAGGAT[G/T]GATGGAATGCAGGGC	114804
rs561151531	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76176470	ATTCTTCTGTAAATC[A/G]ATTTTGCCTACTATT	114804
rs561213700	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76177201	GGGGTGCTGCAGGGG[C/T]TGCATGCTCCACAGA	114804
rs561220424	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76168783	TCCTGAAAAAGGGTG[G/T]GTTGGGAAATAAACT	114804
rs561247939	snp	A/C	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76208991	AAAAAAAAAAAAATT[A/C]ATTTGCTATGTGTAA	114804
rs561288580	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76188018	CATTGCTAAGCTTCT[A/G]AGAGTCTTGAGAGCT	114804
rs561309264	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76235071	GCATTATAGTAATTA[C/T]ATGCATAGTAACTTT	114804
rs561317565	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76228557	CTTACTTACCTCATC[C/G]TACAAGCATATACTG	114804
rs561350045	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76222730	AAGGTTTGAACCGAA[A/G]GTCTGGCTAACTCCA	114804
rs561353614	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76178452	ACTCTCGCTCACACA[C/G]CCCTTGCTGCTCCAT	114804
rs561371089	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76143771	CTTGAATTTTTTTTT[G/T]TTTGTTTGAGACAGA	114804
rs561379999	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147652	GGGGCACCTTCCCCT[A/G]GCAAGGACCCTGAGG	114804
rs561383744	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76217331	TCTGTTAAAAGGAAA[A/C]ATAAATTTACTTATT	114804
rs561402287	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76178062	CTGTGTATCTCATTC[C/T]TCCTTGTTGCAGGAC	114804
rs561468440	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76170290	TGGAGTGCAGTGCTG[G/T]GATCGTGACTCATTG	114804
rs561492379	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76179131	GGGCACAGTAGCTCA[C/T]GCTTGTAATTCCAGC	114804
rs561506711	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76231547	AGGTGATCTTCTGGC[C/T]TTGGCCTCCCAAAGT	114804
rs561521124	snp	A/T	0.00119737	0.0244387	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147071	ATATCCAAACTGAAT[A/T]TGGGATCTTTACTCC	114804
rs561537437	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76169827	CTCAAGTGATCCACC[C/T]GCCTCACCTTCCCAA	114804
rs561701745	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76238962	CTGGCAGACACTCTG[C/T]AGGGATGCGGGCAGG	114804
rs561734689	snp	G/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76185602	AGCCTCCCGAGTAGC[G/T]GGGACTACAGGCACC	114804
rs561762861	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76210807	CACAGCCGCCACCTA[C/T]CTTTCTCTTTTTTTT	114804
rs561791488	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76159748	TCACACACTGTAGAT[C/T]CTGCTTATTGGTAAG	114804
rs561817953	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76205535	ATTGAGACCATCCTG[A/G]CCAAGATGGTGAAAC	114804
rs561905641	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76179497	AGGAGCTTTGAGACC[A/G]GCCTGGCCAACATAG	114804
rs561963657	snp	C/G	0.00318978	0.0398085	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153412	ACCTCCAACACTTCC[C/G]AAGCGATGGCCAGCG	114804
rs561966607	snp	A/T	0.00597247	0.0543191	intron-variant	RNF157	GRCh38.p7	17:76216708	TTCACAATATATTAT[A/T]ATTAGACCCTTGTCT	114804
rs562007401	snp	A/G	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76211315	ACCCACCATTCTTCA[A/G]AGGCCAGTTCAACTC	114804
rs562027637	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76177717	GCCCATAAAAGGCCC[A/C]GGCTCAGCCAGAACA	114804
rs562081127	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76171484	TGAGCCATCATGCCC[A/G]GCCAGATTTATGCCT	114804
rs562083551	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76165735	TGGGCTGGAGTGCGG[C/T]GGCATGATCTTGGCT	114804
rs562132857	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76195161	CAGAAACATATTCAT[C/G]TCACAGAACTCCAGA	114804
rs562185439	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76203699	TAAGGTGACCTCCCC[A/G]CCTCAGCCTCCCAAA	114804
rs562210092	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76238115	AAAATTAAACATTAG[C/T]TAGGCATGGTGGTCA	114804
rs562211756	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142983	CGTGACTATGTGACT[A/G]TCTCCAGATGAAGGA	114804
rs562224228	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76196735	CCTTCTCCAAGAACT[A/G]GGAACCAGAGCCACC	114804
rs562289196	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76166243	GCCTCCCAAACTGCT[A/G]GGATTATACGTGTGA	114804
rs562324029	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76158691	TGTTGACGCTTTAAC[A/G]GAGGAGGAGTACAGC	114804
rs562353160	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76242347	GTAAACGGGACATCC[C/T]TTCCCTTTGTGGGTT	114804
rs562372281	snp	A/T			upstream-variant-2KB	RNF157	GRCh38.p7	17:76241616	ATTTTGTTTTTGTTT[A/T]TCTGTGTTTTGAGAC	114804
rs562374154	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150346	ACCCTAGGGAACCCC[A/G]GGGCTTCTCTCTTCC	114804
rs562411234	snp	C/T	0.00159617	0.0282053	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151430	CGCCTCCAGCCACGT[C/T]GCTGAGCGAGTAAAG	114804
rs562447072	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76208318	AGTTTCTGAGTACAC[C/G]TGGCCTAATTAGCAA	114804
rs562449594	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76175051	AATACCAAAATTAAC[A/G]TTATGGAATACGTAT	114804
rs562451610	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76168367	ATTACTGTGATTACA[A/C]AAACTTATAATCTAT	114804
rs562487662	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76156860	TGCACAGCCTCACCC[A/G]TCCAAGATGGATGCA	114804
rs562489824	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76168988	CTGAAAGCTTACAGA[C/T]GGTCCTCTTTCTCAG	114804
rs562501070	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76198817	GAGGCATACCAGGCC[C/T]CTTGGTCCAGGCCTG	114804
rs562537915	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76162983	TTGCTATATAATCCA[A/C]TTTGAGTTCAGACAT	114804
rs562561975	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76162336	TGGTGGAAACCGAGT[C/T]GGACAGAGCTCTGTG	114804
rs562586471	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76207891	GAACTCTGAAGAGGC[A/G]CTCCAAGAGAACATA	114804
rs562684229	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76182175	GAGAATAACTTAAAT[A/C]CCAAACATCTCAAAC	114804
rs562725440	snp	C/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151302	CTGGAGAAAGTATCT[C/G]TAGAGAATTCCAGCT	114804
rs562762414	snp	A/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149147	CTGGAAGACCCAGAA[A/G]CTTCTTAGGGGGAGA	114804
rs562768102	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194815	GGTCAGGAGATCGAG[A/T]CCATCCTGGCTAACA	114804
rs562783779	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76227333	ACCATGTTGGCCAGG[A/C]TGGTCTTGAACTCCT	114804
rs562796459	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76227738	CAAAATTAGCCGGGC[A/G]TGGTGATGCAGGCCT	114804
rs562798277	snp	C/T	0.00478085	0.0486577	intron-variant	RNF157	GRCh38.p7	17:76220596	TGGGAAGGCCTTGAG[C/T]CCAGAAGTTTGAGAC	114804
rs562807975	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76232798	CCTAATTCTAATAGG[C/T]GTGAAATGGTATCTC	114804
rs562810049	snp	A/G			utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144401	CAAGCTCCGCCTCCC[A/G]GGTTCAGGCCATTCT	114804
rs562877903	snp	G/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76186662	TCAGGTCTGGGCCGG[G/T]GGGGCAGTGGCTCAC	114804
rs562895519	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76160490	AGTTTTTAAAATTTG[A/G]AAGTTGGAAAATGGT	114804
rs562936051	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, downstream-variant-500B	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142242	GGTGGGGGCTGGGTT[A/G]ATTACCCCGCCTCTG	114804
rs562965291	snp	A/C	0.00597247	0.0543191	upstream-variant-2KB	RNF157	GRCh38.p7	17:76240813	GGACGCGTCGCCCCT[A/C]CGCGCCTGTTTATCC	114804
rs563038941	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76196401	AGCTTCTGGGGGTGC[C/T]GGCCATGTGCTACTT	114804
rs563056598	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76212110	GTTGCCTAAAGAGGT[A/G]ACAGGGAGAGATCTG	114804
rs563077427	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76190781	GCATGGTGGCAGGCG[C/G]CCTGTAGTCCCAGCT	114804
rs563130680	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76143045	CTCATCAGGCTGACT[A/G]AGGACCAGCTCCTTG	114804
rs563133321	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76157648	GAACAAATACTTACT[A/G]AGCAACAACAACGTG	114804
rs563249348	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76234796	TATAAAAATTTCTCC[A/C]ATTCTCTGAGTTCTC	114804
rs563262783	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76217582	CAAACAAGATGACTT[G/T]TAGACAGCTTATGCA	114804
rs563306592	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76236723	AAACAACTCACAGAT[A/G]TTTATCAACAGGAGA	114804
rs563309921	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76183674	TATGGATATAGAATA[A/G]TTATAGCTTTCTACA	114804
rs563320436	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76230770	TTGAACCCAGGAGAC[A/G]GAGGTTGCAATGAGC	114804
rs563320602	in-del	-/A	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76238637	AATTCCAAGCTCAGC[-/A]AAAGTATGCTCCATA	114804
rs563328948	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76158288	AGAGGGTGCTGACAA[A/G]GTGTTTGATGAGTGA	114804
rs563339491	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145521	GAGAACGGAGAGAAG[C/G]AGGTGCTGACAGGTG	114804
rs563348957	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76177783	CAACCTACTCCAGTG[C/T]CTCCTCTCTGCTGAT	114804
rs563383791	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145027	AGGTCTCGTGAGCTG[C/T]AGTTCATTGAGTGGC	114804
rs563503395	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76189262	AAGATGTTAACCTTA[A/G]GTGGAGCTGGATAAA	114804
rs563504432	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76184668	ATGGGGAGCCAATCA[C/G]CAGCTTAGAATGAAT	114804
rs563539424	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76182297	AACTCCTCTTTGGCT[C/T]TTGACCCTGGTGCTC	114804
rs563544986	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76231337	TTTGTCTCTATAATA[C/T]TGAGTTGTAAGAGTT	114804
rs563557465	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76225760	CCTCAACTAGGGGAC[C/G]CTTTTCTTCCCCCTT	114804
rs563560216	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76171083	ATTTTTAGTGGAGAC[A/G]GGGTTTCACTGTGTT	114804
rs563621043	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76210355	TCCCAGCACTTTGGG[A/G]GGCCAAGGTGGGCGG	114804
rs563694703	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76217638	CTGTGCTTCAAAATC[A/G]GTGGTGGGGGAAAAG	114804
rs563788052	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76164641	AGGAAAAGGAGAGAG[C/T]AAAAAGTAAAACAAA	114804
rs563821801	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76209833	GGAATGATCTTGGCT[C/T]ACTGCAACCTCCGCC	114804
rs563846444	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76202721	TGGCATAGTACCAAA[A/C]AGTGGCCAATCGAGG	114804
rs563850965	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76194817	TCAGGAGATCGAGAC[C/G]ATCCTGGCTAACATG	114804
rs563909207	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76226344	AGAAGGTGAAGGGGG[A/C]AACCTGGTCGGGTTT	114804
rs563928637	snp	A/C	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76163692	CTCCGTTTTAACAGT[A/C]TGTTGCTAATGCCAA	114804
rs563938797	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76209142	TGCTCAAACTGGACT[C/T]GAATTCTCCTGGGCT	114804
rs563967060	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76157255	CCAGGCGTGAGCCTC[C/T]GCGCCCGGCCAGTCA	114804
rs563989830	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76201957	TCTGTAGGAGAGATT[C/T]GGAGAGGTGAAACAG	114804
rs564041981	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76186429	GGAGAAACACTTGAA[C/T]TGAGGAGGCAGAGGT	114804
rs564054150	snp	C/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76210317	GAAGAGAACCCGCCG[C/G]GCGCAGTGGCTCATG	114804
rs564072938	snp	A/G	0.00636936	0.0560724	intron-variant	RNF157	GRCh38.p7	17:76181683	GAAGCCGAGACAGGC[A/G]GATCACCTGAGGTCC	114804
rs564091286	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76232626	ATAGGAGTGGAACTG[C/T]TGAATCATAAGGCAA	114804
rs564093555	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76180539	GCATTATGCTAGGTA[C/T]TTTAGATAGATTCTT	114804
rs564115454	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76218458	TCAGCCTGGGCAACA[C/T]AGCAAGACCTCATCT	114804
rs564152608	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76226829	TGCTTTGCTGGAATC[A/G]AGTAATGTGCTTAAT	114804
rs564167588	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76206170	TAGGAAGTCGAGGCT[A/G]CAGTGAGCTGTAGTT	114804
rs564248474	snp	A/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151526	GATTCAAACAACACG[A/G]TGTGAAGGACAATTT	114804
rs564254617	snp	C/T	4.53361e-05	0.00476088	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76173761	CAGAGTCTTCACGGG[C/T]TCTTGGGGAGGTGGG	114804
rs564272450	in-del	-/TTTAT			intron-variant	RNF157	GRCh38.p7	17:76231713	CATCAAGCTCTTGTC[-/TTTAT]TTTATCCAAAAGGCA	114804
rs564306944	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76211899	TCATTCATTCAACAA[C/T]CATTTATTAAGGGCT	114804
rs564335368	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76234351	TTCATGTGCAAGTTT[C/T]TATGTGAATGTATTT	114804
rs564352362	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76239126	CACCAAAATCTCCAT[C/T]GGGTCCTAAGCAGAC	114804
rs564406487	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147704	GCTGCTCCCTCCTCA[A/G]CCTCATTCTCACAGT	114804
rs564414732	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76239718	GCAAGTGCCTGTTTG[C/G]ATGCCGAGGTCGCCT	114804
rs564424314	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76199284	CTCCCAGTGTACTTA[C/T]ATTCCAAATTGGTTT	114804
rs564439644	snp	A/G			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147843	AGATTCAAAATCCTT[A/G]GAGGGAAATGGATAA	114804
rs564459144	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76165820	TATCTGGGATTATAC[A/G]CATGAGCCACCATGC	114804
rs564495130	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76166315	AGGAGCTTGGAGTCA[C/T]AGATGTGAGAGGATG	114804
rs564506647	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76171712	ACCACCATGAAAGGT[A/G]AAGTTGATTATCACC	114804
rs564531543	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76166714	TTAAAAATGTCATAG[A/G]TGTAAATAAGAACCT	114804
rs564594013	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76232233	ACAAAACATAAATTT[A/T]AAAAATTAGATGGGA	114804
rs564624408	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76191906	TAGGGACAAAATTTA[C/T]GTGTAATCAACTGTT	114804
rs564686232	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76201744	TCAGTAAGTCATGTG[A/G]TTGTGGACATATTGC	114804
rs564723263	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76189505	GAGCTCCATAACAGC[A/G]ACCTCAAAAGTTGTG	114804
rs564730930	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154544	TTAGATCCGAGCCAC[A/G]TTACCCATATATGCT	114804
rs564745652	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76235549	TAATATTAAATTGAT[A/G]CTCCTAAAGCTAGGA	114804
rs564765033	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76192478	TAGTGATTAGACCAG[C/T]ACATACAGAAGGCAG	114804
rs564808525	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76236190	TCTGTAGTAGGTTTA[C/T]TTCTTAAAGACTTCA	114804
rs564839254	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145480	CTGAGACTCCGATGA[C/T]GGTGCGAGCCACAGC	114804
rs564844626	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76173984	GCGGGAAAACTGGGA[C/T]GCAATTTGGGGCCCA	114804
rs564846058	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76201846	TTTAACCATTCCACT[A/G]TAATGGCCATTAGAT	114804
rs564860756	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76169713	GCCTCCCAAGTAGCT[A/G]GGATTATAGGCGTGT	114804
rs564884137	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194929	CTGAGGCAGCAGAAT[A/G]GCGTGAACCCGGGAG	114804
rs564888712	snp	A/C	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76193751	CAATCAGGAGCTGAG[A/C]GAGAAAACAAAACAG	114804
rs564905591	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76164260	ACAAGGTGCTGATCA[C/T]TCTGGAAGAGGGAGA	114804
rs564910389	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76202361	CTGTTCCTTGGAGTG[C/T]CCTTTGCCTCAACTC	114804
rs564930985	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76157209	CTGACCTCGTGATCC[A/G]CCCGCCTCGGCCTCC	114804
rs564936064	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76163490	ATGAGCCATCAAGCC[C/T]GGCCAGCCCTGTTTC	114804
rs564945536	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76156944	CTTTTGTCTTAGTTC[A/T]CGCAGTCCTTCTTTT	114804
rs564959298	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76152005	CTTCGTAGAGAGGTG[A/G]TGTCTGTCTGCTCAA	114804
rs564971420	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76200978	TGGCACACATCCCAA[C/T]CCCAGCGAGCAGACC	114804
rs564984951	in-del	-/CTT			intron-variant	RNF157	GRCh38.p7	17:76202911	TTCCTAACTGGTCTT[-/CTT]ATTTTCTGTCTCTCT	114804
rs564997976	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76211970	ACAGTAAAAACAGTC[C/T]TTGCCTTATGAAACT	114804
rs565007786	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194825	TCGAGACCATCCTGG[C/T]TAACATGGTGAAACC	114804
rs565010869	snp	C/G/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76232715	CATTTCCCATAACAC[C/G/T]TCATAAAGATTCCAA	114804
rs565030456	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194257	AGTCCCTGGCAACCA[C/T]TGATCTATTTCTTAT	114804
rs565133129	snp	C/T			upstream-variant-2KB	RNF157	GRCh38.p7	17:76242121	CTCCAGGGCTTTCAG[C/T]CATCCCTGTGGGAGG	114804
rs565154142	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76230257	CTGTCTAATTTCCCC[A/G]GATCTTGAGGCAAAG	114804
rs565160370	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76229597	TTTTCATCCAGATAG[A/C]CCATCTTTGCCTCAA	114804
rs565199181	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213075	TTAAAATACCTCCAG[A/C]CAAAAGACCAAAAGG	114804
rs565207689	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76189845	ACAAACAAAAACAAC[C/T]GAAGGCTGAAACAAA	114804
rs565258011	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213924	GAGACGGCATAGAAG[C/G]TCTGTGCCCCTTCTC	114804
rs565274624	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	RNF157	GRCh38.p7	17:76240845	GGCTCGGATTACCGC[A/G]CAGGGAGCCGCCCCC	114804
rs565364279	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76196290	TTAAAGAGCAAATTG[A/G]ACACAGTTCCACTTA	114804
rs565388518	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76171956	TGTGCCATATGTGAT[A/G]AGAGAAACCAAGTGG	114804
rs565396571	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76222044	ACAAACTGCTTAATT[G/T]GTTTTATTTTGAGGT	114804
rs565464247	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76227802	GAATCGCTTGAACCC[A/G]GGAGGCAGAGGTTGC	114804
rs565487032	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76175972	TGTTTATAAATCCAC[A/C]CCTATACTTTAGGCT	114804
rs565529541	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76170031	ACAGCAGGACTTGGG[A/G]ATCCTGGGCTTCACT	114804
rs565549183	in-del	-/T	0.177182	0.23916	intron-variant	RNF157	GRCh38.p7	17:76209069	CCAATGTTGATGTTC[-/T]TTTTTTTTTTAAGTG	114804
rs565562915	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76180689	CTCAGCTTCCCAAAG[C/T]GCGGGGATTAGAGGT	114804
rs565567268	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76224909	GGGAGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC	114804
rs565579437	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76224395	AACCCATTTTCTATT[A/C]TTCTACAATTCTATG	114804
rs565616165	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76169100	CACTGATGATTTCCT[G/T]CCTTTTACATTCTCT	114804
rs565616584	in-del	-/T	0.366885	0.220993	intron-variant	RNF157	GRCh38.p7	17:76165683	TTATATAACCCATAC[-/T]TTTTTTTTTTTTGAG	114804
rs565631339	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76177454	ACATGCTCGGGGTAG[C/T]GCTGACAAGCCAGCC	114804
rs565656894	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76230420	CTGAACATGTGCTCT[A/G]TGCAAAGCATCCTGA	114804
rs565667863	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76171390	GACGGGTTTTTACCA[C/T]GTTGGCCAGGCTGGT	114804
rs565670583	snp	C/T	0.0023933	0.0345097	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145549	GTGCAGAGCCTGCTC[C/T]TGCCCCCTGGGCTAG	114804
rs565739270	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76163247	ATCCAGGCTGGAGTG[C/T]AGTGGCACCATCTTG	114804
rs565798501	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76177952	ACACTTGTCAGGACA[C/T]CCTGGCTGCGGAAAG	114804
rs565877023	snp	A/T	0.00597247	0.0543191	intron-variant	RNF157	GRCh38.p7	17:76163891	TGCTCTTAAAACTTG[A/T]TTTCATGCAGTGATT	114804
rs565885552	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76165876	AGAGACGGGGTTTCA[C/T]TATGTTGGTCAGGCT	114804
rs565898713	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76169987	CTTGTATTTAAGATA[C/T]TTAAACTGCTGATTA	114804
rs565928497	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76222218	GGGTGTAGTGGCACA[C/T]GCCTGTGATCCCAGC	114804
rs565950698	in-del	-/AG	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213870	AGAAAGCTTCCAAAC[-/AG]GGGAACACTTACAGG	114804
rs566014021	in-del	-/AA	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76225383	AAAATTAGTATATAT[-/AA]GTTAATAATTTAAAA	114804
rs566045331	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76190239	TGGCACAATTTCGCC[G/T]CACTGCGACTTCCAC	114804
rs566047189	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76182685	CCATCCATAAAAATA[A/C]AGTTAACTTCAACAT	114804
rs566127687	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76201317	ATAGTGAGACCCTAG[C/T]CTCTACAAAAAAAAA	114804
rs566134987	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76160026	GATCTCACTATGTTG[C/T]CCAGGCTGGTCTTGA	114804
rs566180135	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76195001	GCCTGGGTGACAGAG[C/T]GAGACTCTGTCTCAA	114804
rs566266413	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76190974	CCCGGCACTTTGGGA[A/G]GCCAGGAGTTCAAGA	114804
rs566276321	snp	C/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76154837	GCTAGACTGGGCTCC[C/T]AGATGGGTGCAGTGG	114804
rs566280985	in-del	-/TTTT			intron-variant	RNF157	GRCh38.p7	17:76227110	AATATTAATAACCTC[-/TTTT]TTTGTTTTTTTTTTT	114804
rs566281159	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76235774	ACTGCTTTGGGACCC[C/T]GAGGTGGGAGGACTG	114804
rs566324323	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152761	AGAATACTAGAGCGA[A/G]CAGAGCTGGGCAGAG	114804
rs566338222	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76193935	CAGCCCTGGGGGACA[C/T]GGCTACCACTTCTCT	114804
rs566340296	snp	C/T	0.00597247	0.0543191	intron-variant	RNF157	GRCh38.p7	17:76229795	TGCTCCTTGATGGAA[C/T]CTAAACTGCTTGTAA	114804
rs566344099	snp	C/G	0.00755907	0.0610114	intron-variant	RNF157	GRCh38.p7	17:76236869	AGCAAACAGAGCAAG[C/G]TGTAGAACAGTCTAA	114804
rs566368298	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151653	AACTAAAAAGGCACT[C/T]GGTGCTTAAAGTGTG	114804
rs566370581	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76211585	TATAAAACCCTTAGA[A/G]CAGTGCTTAGAACAT	114804
rs566427006	snp	C/T	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76186810	CCAGGCATGGTAGTG[C/T]ACATTTGTAATCACA	114804
rs566431780	snp	A/G	0.00517822	0.0506191	intron-variant	RNF157	GRCh38.p7	17:76198587	GGTTCTGCCGTATAC[A/G]TCAGTGTCCTCTTCA	114804
rs566463817	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76179922	AGTTTCTGTTTTCTT[C/T]TTTAGAGTCTGCAAA	114804
rs566532980	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76238369	AAGACTTCTCTCATG[C/T]ATAACTTCTGATTTA	114804
rs566550193	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76240946	CCGCTCCGCTGCTCC[C/G]GCGCCTGGAGGAAGC	114804
rs566559092	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76206437	GATTCACAGATACCT[C/T]AGTTCCTTTATATAA	114804
rs566597166	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76198953	TCTGTGCCTCTGCTC[A/G]TGGGCCCTCCTCCGA	114804
rs566608344	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149692	AAAAGGCAACCAGAG[G/T]TTTTGAGACATCACT	114804
rs566620921	snp	A/C	0.00398564	0.0444627	intron-variant	RNF157	GRCh38.p7	17:76193492	AGAATTATTGTAGAT[A/C]TGCCCTATATTCTAC	114804
rs566669048	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76228257	AGAAAGGCACACATC[A/G]ATGCGTCTAAAACCC	114804
rs566700835	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76232302	CTGAGGCTGGAGGAG[C/T]GCCTGAGCCCAGTAG	114804
rs566717213	snp	A/C	0.000798403	0.0199641	utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142711	TGAGGTGGGCAGGAC[A/C]CTAACTCCCAGGCCA	114804
rs566724168	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76180826	AACATTCACATTCGC[A/G]TTATCGTGCGGCCAT	114804
rs566740383	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76227050	GAAGGCGTGCACGTG[C/T]GGAAAAAACTACATC	114804
rs566742257	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76233656	ATCCTTCTGCCTCAA[C/T]CTGCCGAGTAGCTGA	114804
rs566762210	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76226416	GGGGGGGCACCTTAT[G/T]AGTCTCCTGGACTAG	114804
rs566775540	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146595	TCCCAGTGGCCTCCC[C/G]TCACGAGGCATCTCT	114804
rs566792398	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76191397	GCGGGAGGATCATGA[A/G]GTCAGGAGTTTAAGA	114804
rs566801822	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76216665	TCAAAGTGGTGTTGT[A/G]AATCTATATCTACTG	114804
rs566896780	snp	C/T	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76197693	CCCACCTCAGCCTCC[C/T]GAGTGCTGGGATTAC	114804
rs566918470	snp	C/G	0.00438332	0.0466095	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147381	ATGCACAAATAAAAA[C/G]AGCAGCACCACCACC	114804
rs566934884	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76191962	ACAATACAATACAGA[C/T]TTTTATATAACAGTT	114804
rs566938128	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76203806	GGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG	114804
rs566939265	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144155	AATTATGGTAATATA[A/C]GACCACTCCTCACCC	114804
rs566990334	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76228902	GGACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC	114804
rs566993707	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76217916	TAAACCGTAAGGTAT[A/G]AGTGGGAAGGAGAAA	114804
rs567023712	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76185675	GGGGTTTCACCGTGT[C/T]AGCCAGGATGGTCTC	114804
rs567025757	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76178646	AGATCACATAATACT[A/G]TGTGCCAGGCACTAT	114804
rs567076155	in-del	-/AAATAAAT	0.00755907	0.0610114	intron-variant	RNF157	GRCh38.p7	17:76186941	TGAGACTCCGACTCA[-/AAATAAAT]AAATAAATAAATAAA	114804
rs567100124	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76148075	GTTTGAAATTTTCCT[C/T]AGTGCCCACAAAGTG	114804
rs567104085	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76229646	CTGGAAGGAGGAGGA[A/T]TCAAGGGCACTTTAT	114804
rs567106712	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76218805	CGGGAGTGATGGCAT[A/G]TGTCTGTAGTCCCAG	114804
rs567188534	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76156872	CCCGTCCAAGATGGA[C/T]GCAAAGTTCTACGAA	114804
rs567214936	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76188192	TCTAGATGGTGAACA[C/G]CCATACTCTATCATG	114804
rs567235408	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150847	CTCCCAGGTGTGTGC[A/G]TGCCCAGCAAGCTTG	114804
rs567248066	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76188686	GTCATTAATACAAAC[A/G]TTCTCTTATGCTAGT	114804
rs567253516	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76157030	GGAGTGCAGTGGTGC[A/G]GTCTTGGCTCACTGC	114804
rs567287050	in-del	-/AG			intron-variant	RNF157	GRCh38.p7	17:76230894	AAGAGAAAGAGAGAA[-/AG]AGAGAGAGAGAGAGA	114804
rs567290155	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151578	ACATTTGACTCAGTC[C/T]GCTTGGGCAAGATGT	114804
rs567320035	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76218409	ACTTTGGGAGGCCAA[A/G]GCAGGAGGATTGCTT	114804
rs567412934	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76174480	TAAAGAAAGGGGAAA[C/T]AGCCAAAAATTTCAC	114804
rs567439101	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76176182	GGCCCTGCTCTTTCA[C/G]GAAGCTGCATTATAA	114804
rs567441105	snp	C/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76182481	TGTGTGTGTGTGTGT[C/G]TATCAATCACATGTC	114804
rs567465019	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76209447	GCCCAACAGAAACTC[G/T]TAAACTTTCTTAAAA	114804
rs567495522	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76170592	TGGTACAAGGGAGAG[A/G]ATCTGCCTACCTTGA	114804
rs567548092	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76143220	GGAATCTTTCCGTGC[C/T]TCTCCCTAGGAGAGG	114804
rs567604355	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76221622	GGACTTTCTTGGTAC[C/T]AGCTATTGTTCATGC	114804
rs567645731	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76227435	CTATAATCTCTTCAG[A/G]GGACTGACTCTATAA	114804
rs567657222	snp	A/T			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212542	CAACCTAAATCTAGT[A/T]AAAAAAAAAAGCTGA	114804
rs567668766	snp	C/T	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213292	TTGGAATATCCAGGC[C/T]GGCATGGTGGCTCAT	114804
rs567688691	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76178003	CTCTGAGCTGTTCCA[A/T]GGCTCAATAAGGCTC	114804
rs567690455	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76220717	GTAATCCCAACACTT[C/T]GGGAGGCCGAGGTGG	114804
rs567711353	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76174395	TCTTCATCATTTACC[A/G]TCCGCTTCTTCCCCC	114804
rs567726619	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76169129	CTGTTCTCTGTAGAA[C/T]CCGTTAGTTGGATGT	114804
rs567749446	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76172427	AGAAACTCTGTCTCT[A/C]CTAAAAACACAAAAT	114804
rs567772663	snp	C/T			utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144528	TAGCCAGGATGGTCT[C/T]GATCTCCTGATCTCA	114804
rs567829095	snp	A/G	3.29837e-05	0.00406088	stop-gained, nc-transcript-variant	RNF157	GRCh38.p7	17:76161624	TTTTCCTCATGGCTC[A/G]GATCTGAAGCAGTGC	114804
rs567860710	snp	A/G	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76172660	GTCTCAAATATATAT[A/G]TATATATATCAGACA	114804
rs567865625	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76234121	ATTTCTTATAAATGA[C/G]ATTATTCAATAGATG	114804
rs567889770	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76235649	TGCAATAGGAAAGAC[C/T]CATTTGACAAGAATA	114804
rs567912769	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76187340	AGGTGCATGACACCA[C/T]GCCCAGCTAATTTTT	114804
rs567960023	snp	G/T	0.00279162	0.0372561	intron-variant	RNF157	GRCh38.p7	17:76204799	TTTTTTTTTTTTTGA[G/T]ACTGAGTCTCACTCT	114804
rs567998723	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76197890	GACTTGAGATGGGAA[C/T]GTCTGTGTATATTTA	114804
rs568003876	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76220829	TGGGTGTGGTAGTGT[A/G]CACCTTTAATCCCAG	114804
rs568004154	snp	A/C	0	0	intron-variant, nc-transcript-variant	RNF157	GRCh38.p7	17:76156470	GAGGCCGCAGCTTCT[A/C]TCTTCCGTCCTCACT	114804
rs568018992	snp	C/G	0.0123036	0.0774623	intron-variant	RNF157	GRCh38.p7	17:76210387	TCACGAGGTCAGATC[C/G]AGACCATCCTGGCTA	114804
rs568145992	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76158560	TAAAGAACAGAACTT[A/G]CTGCAAGGGGAGCTG	114804
rs568165271	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76210458	AGCCGGGTGTAGTGG[C/T]GGGTGCCTGTAGTCC	114804
rs568242062	snp	A/T	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76225628	TGTATTTATGGCATG[A/T]CCTCATTGTTTTTAG	114804
rs568316856	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154174	TCTAACAGCCCCATA[C/T]AACTGAGCAGCGCCA	114804
rs568346336	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76164085	CTACCCAGCTGCTCT[A/G]CACCCTCCGTGAGAT	114804
rs568446616	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76177499	CCCCTTCCAGACTTT[A/G]GGCACTGATGAGCAT	114804
rs568461753	snp	A/G	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76165129	ATGAGGGTTCTGTAC[A/G]ATCTGCAGTTTCAGG	114804
rs568470102	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76209946	TGTATTTTTAGTAGA[A/G]ATGGGGTTTCACCAC	114804
rs568513480	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76202266	CTATTAGGCCAGTTA[C/T]TCCAAGTCCAAGGCA	114804
rs568528749	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76155178	CTGGCCCTGGTCCTT[A/C]CTGGCATCCCCAGCC	114804
rs568550255	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76195131	GAGAACAGAAAGGGC[C/T]GAAATCCCAAATGGC	114804
rs568550994	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76236995	GAGAACCAGGTGGAT[A/G]GACAACAGCGGTGAG	114804
rs568552196	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76202988	TAAAATGCAAATTAG[A/G]TTGTAATAGTTATCT	114804
rs568662758	in-del	-/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76166742	CCTCTAACCTATAGA[-/T]TTTTTTTTTCTTTGA	114804
rs568698637	in-del	-/T/TT	0.19334	0.243495	intron-variant	RNF157	GRCh38.p7	17:76168428	TTAGTGCTCATCCTA[-/T/TT]TTTTTTTTTTTTTCT	114804
rs568701476	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76194107	CAGTAAAATTCAGCC[-/T]TTTTTGGTGTACAGT	114804
rs568738119	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76231050	CTGAGGCGATCCTCT[G/T]GTTTGTGCCTTCTGA	114804
rs568778007	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76143907	TCCCGAGTAGCTGGG[A/G]AGGGCCCTTGAAGTG	114804
rs568785635	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76240086	GGGCCCCCTCAGGCC[A/G]TCCCGACCCAGACCC	114804
rs568829897	snp	A/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149001	GCTTAGCGTGGTCTC[A/G]CAATTCTAGTCTTAC	114804
rs568848011	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76174544	CAAATGTTCCCGGTA[C/T]TTTTAAAATGTTATT	114804
rs568908832	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76235321	TCCTGCCTCAGCCTC[A/C]CGAGTAGTTGGGACT	114804
rs568916216	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76199016	CAGGCAGGGACTGCA[C/T]TTCATCGGTATTTCT	114804
rs568955023	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76199721	TTGGTGACGCAGCTC[A/G]CTGGTCTCCATCCTA	114804
rs568957022	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76193561	CCCCACCCACGGACA[A/C]ATACAAGTTTCTACC	114804
rs568968680	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76234410	GAGTAGAACTGCTGA[A/G]TCATCTAGTAACTAG	114804
rs568980279	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76226443	CTAGGGGGGCAAAGA[G/T]ATTACAAGTGTCATC	114804
rs568991010	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76187630	ACAGGTTCTCACTCT[A/G]TCGCCCAGGCTGGAG	114804
rs568994432	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76199296	TTATATTCCAAATTG[C/G]TTTTGGCTGGAGTGC	114804
rs568995703	snp	A/G	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76193936	AGCCCTGGGGGACAC[A/G]GCTACCACTTCTCTG	114804
rs569031893	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76233761	TGCTCTTGAACTCCT[A/G]GGCTTAAGCCATCCT	114804
rs569052393	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76188059	TTCAGTCACCCCCCA[A/G]TAGCAGTGGGCAGCC	114804
rs569053278	snp	A/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151970	TCACTTTTAAAGGGC[A/G]CAGGCAATCCTTCCA	114804
rs569064382	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76143247	GAGGACTAAGCACCT[A/G]CTGCGAGGAAGGACA	114804
rs569093429	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76181322	TGCTTAGATGGCAGT[A/G]TGTACAAAATCATAC	114804
rs569114055	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76185273	CAGGCTAAAACCTTC[C/T]ACCCAATCATGCTGT	114804
rs569151086	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76220108	GGTGCCGCTAGCATC[C/T]AGCCTGTAAGTCTGC	114804
rs569152938	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76231991	ATATAAACAAACTCA[C/T]ACGATATATAGTCTT	114804
rs569189995	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76192799	TATGATATCAACAGC[C/G]AGAAGACACAGGTTC	114804
rs569218497	snp	C/T			intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153766	TGAAGAAACTTGGAC[C/T]TGTCTCCTTGACCAC	114804
rs569231589	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76239356	AATCCAGAGGCTAGA[A/G]ACATTTAAGTGAAGG	114804
rs569288646	in-del	-/CCCCTG	0.0103295	0.0711199	intron-variant	RNF157	GRCh38.p7	17:76240098	CCGTCCCGACCCAGA[-/CCCCTG]CCCCTGCCCCTGCCC	114804
rs569305446	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76222075	GATAAAAATGTTCTA[G/T]AGGCCGGGCGCAGTG	114804
rs569328939	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76185749	GCTGGGATTACAGGC[G/T]TGAGCCACCGCGCCC	114804
rs569347587	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76218608	CACCCCTGGACTCCA[G/T]CCTGGGCAACAGAGT	114804
rs569382511	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76223210	TTTTTTTTTTTGAGA[C/T]GTAGTCTCACTCTGT	114804
rs569410974	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76179331	CCCAGGAGATTGAGG[C/T]TGCAGTGAGCTATGA	114804
rs569489775	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76211662	TCAGTTCTCTCGCTT[A/T]TAAAATAGAGTGATA	114804
rs569495343	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76224185	ACAAAAAAGAAAAAT[C/T]TCATTTAAAATTCAT	114804
rs569498144	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76215275	TTAGCAAGCTTAGCA[A/T]GACCTTGTCTCTACT	114804
rs569609835	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76167200	AACTTCCTCTGCTCA[C/T]GCCTGTTCTCAATTA	114804
rs569633107	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76228950	AATAATACAAAAAAA[A/G]AAATTCACTCACCCA	114804
rs569647151	snp	A/G	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76182573	TTTTGCTGTAAAAAA[A/G]TATGGTCACAGTACA	114804
rs569660225	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76152127	AGTTTTGCTTCTTTC[C/T]TCCTATCCTAATACT	114804
rs569685648	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76176838	TGCTTCAGGGGCCCC[A/G]GGCAGGAAGTGGGAG	114804
rs569689417	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76175430	GCCAAACAGTTTTCC[A/G]CAAAGCTGACTCCAA	114804
rs569698837	snp	C/G	2.31404e-05	0.00340142	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145232	AAGTGCAGAGGCTGG[C/G]GCTCAGACAGCCAAA	114804
rs569732057	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76158324	AGCAGAGGGACCTGA[C/T]GAGGCATGCAGGTAG	114804
rs569809414	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76210038	GCTGGGATTACAGAC[A/G]TGAGTCACCGTGCCC	114804
rs569855953	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76203135	GGCTGGGATTACAGG[C/T]ATGCACCACCATGCC	114804
rs569863035	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76169933	CTGTCTTTCCTATTA[C/T]AGGCATTCCTTACAC	114804
rs569876987	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76164283	GAGGGAGAATGGATG[A/G]CTAACTTTGAATTTT	114804
rs570071035	snp	A/C	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76208634	CATTTTTATGCAGCT[A/C]TATGAAGTTACTCTG	114804
rs570077903	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76172834	CATATCATCTAGGGG[C/T]GGCGGGCAGTGGGAA	114804
rs570108566	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213378	AGTTAGAGACCAGCC[G/T]GGCCAACACGGTGAA	114804
rs570122173	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76214147	CATCAGAAGTGGGGG[A/G]CAGTCTTGTGAGATT	114804
rs570123674	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76173235	AGCGTGCAGTGAGCC[A/G]AGATTGCGCCACTGC	114804
rs570139866	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76200517	TACCTAGAGTAGTCA[A/G]ACTCATAGAGGCAGA	114804
rs570145757	snp	A/T			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212831	CTAGCACTACACTCC[A/T]GTCTGGGCGACAGAG	114804
rs570169339	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76157037	AGTGGTGCGGTCTTG[A/G]CTCACTGCAACCCCT	114804
rs570180754	snp	C/T	6.65402e-05	0.00576764	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76162617	GGAGGTAGCTGACCC[C/T]GTCTACCTGAACAGC	114804
rs570209309	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76156523	GCCTCCCAGGGGAGG[C/T]GCACACTTCAGTCAA	114804
rs570353444	in-del	-/AAAAG	0.00398564	0.0444627	intron-variant	RNF157	GRCh38.p7	17:76215495	AAAAGAAAGAAAGAA[-/AAAAG]AAAAGAAAAGAAAAG	114804
rs570358846	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76235332	CCTCCCGAGTAGTTG[A/G]GACTACAGGCTTCTG	114804
rs570393896	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76192887	GCTCTCTTGCACAGG[A/G]TGACTGCGATGGCCA	114804
rs570417094	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76204957	GCCCAGCTAATTTTT[A/G]TATTTTTAGTAGAGG	114804
rs570431452	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76186015	AGCAAGTATTTGAAC[A/G]TTCTAATGCCAAGTA	114804
rs570448543	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76217881	AAGTCACATCATACA[C/T]ATATCTCCAAGATTA	114804
rs570455480	snp	C/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76197954	TGCAAATAGCCCTCT[C/G]CCTTGAAGATGGGAG	114804
rs570531334	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76205605	TGGTGTGTGCCTGTA[A/G]TCCCAGCTACTTGGG	114804
rs570532857	snp	C/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76237093	CAAAAATAAATAATT[C/G]TAAATAATTTAGGCT	114804
rs570561613	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145933	CTCCTCCTGCACCTA[C/T]GCAGCTGTTGAGGTT	114804
rs570606380	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76155114	ACCCACATTCCACTT[C/T]TCACTGATCTAGGCA	114804
rs570613987	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76159846	AGTAAGGAAAAAAAA[A/T]CACCAGTAATCAAAT	114804
rs570658031	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76202942	CTGATTCATTACCTA[C/T]ACTGTGAATTAATTT	114804
rs570681950	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76239434	CCCTGTCCCAGAGCT[A/G]GTCCCACTCCAAAAC	114804
rs570685861	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76175158	GCAGTTTCTTTTTCA[C/T]CTAAAAAGATGTGGT	114804
rs570701140	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146544	GTAGGGAAGGCATGT[C/T]GTCCTCCGGACCCTG	114804
rs570710313	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76148128	TTTTGAGGCCTCTCA[A/G]AAAGAGGAGAGAATT	114804
rs570792316	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76239902	AATGGAGGCCGCTCC[C/T]GTCCTCCCGTGGAGG	114804
rs570837940	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76172098	TTGAATCTCTCCTCC[C/T]CAGAGTTGACCCTGG	114804
rs570899682	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76196142	GAGCTGTAACACTGC[C/T]GCCTCAATAAAGCTG	114804
rs570900619	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241158	TACATGCTGTTTAAG[C/G]CTCCTTGTAGCCCTA	114804
rs570911081	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76184293	TAGAAACCAACACCT[A/G]GGGTCATATCAAAAA	114804
rs570914705	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76233906	AGTGTGTACAATCCA[A/G]TGGTTTTTAGTATAT	114804
rs570914807	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241771	GTGCCACCACACCCG[C/G]CTAATTTTTCTACTT	114804
rs570930624	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76225840	CCAGGGAATCTGCCC[C/T]CTCTTTTAGAGCCTC	114804
rs570938773	snp	A/C	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76190383	TGTTGGCCAGGCTGG[A/C]CTCAAACCCCTGGCC	114804
rs570938864	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76196868	AGATGAAGCAACTCT[A/G]TGGTACAAGCTGTAC	114804
rs570973458	snp	A/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76191310	GTGAGACACCGTCTC[A/T]ACAAAAAAATAAAAA	114804
rs570975996	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76234642	TCATCTCTTCAAGTG[C/G]TTATTGTCCACTGTA	114804
rs571036421	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76231625	AGTGAGACCCCATCT[C/G]CACTTATTTAAAAAA	114804
rs571107183	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76235220	TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT	114804
rs571109160	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144004	GAACTTAGCTCAAGG[C/G]TCTCCATCACTTCCT	114804
rs571116089	snp	A/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76185127	TCATTGTTTGAGAAT[A/G]CTGAGACTGGGCAAC	114804
rs571131978	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76217132	AAATGTGCAAGATTG[C/T]ATGAATTAAAAAGAG	114804
rs571135174	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144597	CAGGCGTGAGCCACC[A/G]CGCCCGGCCAAGAGC	114804
rs571180716	snp	C/T	0.000118384	0.00769273	intron-variant, utr-variant-3-prime, nc-transcript-variant	RNF157	GRCh38.p7	17:76156361	AGGACATGGAGCAAG[C/T]GCCAGTCACCTGTGC	114804
rs571209335	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157	GRCh38.p7	17:76155908	AAATTCTGCTCCTTT[A/G]TATTTTAGAGCTCAG	114804
rs571213081	snp	A/G	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151435	CCAGCCACGTCGCTG[A/G]GCGAGTAAAGCACTG	114804
rs571246294	snp	A/G	0.00279162	0.0372561	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149891	ATACAAAAATTAGCC[A/G]GGCGTGGTGGCGGGC	114804
rs571306675	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76210470	TGGCGGGTGCCTGTA[C/G]TCCCAGCTACTCAGG	114804
rs571327729	snp	C/T			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213113	ATGCACATTAATGAT[C/T]ATATATATTTTTTGG	114804
rs571343445	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76209403	AGCTTGTCCAACCTG[C/T]GGCCCAGGGGTAGAT	114804
rs571363639	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76228832	AGGCTGAGGCAGGCG[A/G]AGAATCACCTGAACC	114804
rs571366592	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76172634	AAAAAAAAAAAAAAA[G/T]GCGAGACTCTGTCTC	114804
rs571378952	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76188115	CTTTCTTTGGCTTTT[A/C]TGAAAGTCTAAACTC	114804
rs571397058	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76157069	CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA	114804
rs571397268	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76228120	AAAAACCATTTATGG[A/T]ATATTCCATTTCCCC	114804
rs571423941	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76181359	CCACACTCCTTTCTA[G/T]CTTTAACAGGAGTAT	114804
rs571476734	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76176129	ACATGCAACACTCCA[C/G/T]GCCAGGAGTAAGGAG	114804
rs571491124	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76191968	CAATACAGACTTTTA[C/T]ATAACAGTTTCAGTA	114804
rs571501413	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76179353	GAGCTATGATAGCAT[C/T]ACTGCACTCCAGCTT	114804
rs571550154	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76226594	CTCCTTGCTGTTGTT[A/G]GAGGGACTGACCAAC	114804
rs571559148	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76181845	CCCAGGAGGCAGAGG[C/T]TGCAGTGAGCTGAGA	114804
rs571572557	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76207379	AGTGAGCAATGATCA[C/T]GCCACTGCACTCCAG	114804
rs571609920	in-del	-/G	0.00755907	0.0610114	intron-variant	RNF157	GRCh38.p7	17:76236868	AAGCAAACAGAGCAA[-/G]GTGTAGAACAGTCTA	114804
rs571625860	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76226944	TGCAGAGCCTGGTGC[C/T]GCTGCCGCCGCTGCA	114804
rs571630495	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76208063	TGGGACTAGAGGCAT[A/G]CACCACCACGCCTGG	114804
rs571665084	snp	C/T			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152627	ACAAGAAAGGAATCA[C/T]GTTGTGTGGGCATGT	114804
rs571666029	snp	G/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76232922	ATCTATTGAAATCTC[G/T]CATATTTTTTTTTTT	114804
rs571680941	in-del	-/C	0.0104185	0.0714191	intron-variant	RNF157	GRCh38.p7	17:76239540	TTTCCACCACCACCA[-/C]CCCCCCCACCCCCCG	114804
rs571693281	snp	A/T	0.00478085	0.0486577	intron-variant	RNF157	GRCh38.p7	17:76160125	ATGCCTGGCCAGAAC[A/T]TAAATATTTTCCTTT	114804
rs571703631	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76179834	ATTCAGGGCCAAGCA[C/T]TTTTCTGAAGTACTC	114804
rs571759907	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76209747	TATTAATAGAAGAAA[C/T]GGCTACTTTCATTTT	114804
rs571767032	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76224302	GGGTTCCCTAAATTA[C/T]GTCTGCCTCAATAAG	114804
rs571774994	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76206652	CTAAAAATACAAAAA[A/G]TTACCTGGGCATGGT	114804
rs571867988	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76238160	CAACGGTTCCTTTCA[C/G]GACTAATACTGTAAT	114804
rs571923029	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76236321	ATTATGCCTATTTCT[C/T]CCTGGATAGAGAAAA	114804
rs571949336	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76216722	TAATTAGACCCTTGT[C/T]TCGACAAAAAATTAA	114804
rs571959649	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76203339	GGTAATTTTATAGAT[A/G]GGGAAATTGAGACTC	114804
rs572000909	in-del	-/T	0.310878	0.242475	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76148262	CAAATTATCTTTGCC[-/T]TTTTTTTTTTTTTTT	114804
rs572010566	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76219564	GGACCAGACAGAAGG[C/T]AGATTTCTTTGAATA	114804
rs572010890	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76193018	TAGAGACGGGACCTC[A/G]CTGTTTCCCAGGCTG	114804
rs572045868	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76215382	CAGAAGGCTGACGCA[G/T]AAGGGTCGCTTGAGT	114804
rs572074636	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76162353	GACAGAGCTCTGTGG[C/T]AGAACAAAGCCAAAC	114804
rs572122053	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76198978	CTCCGACGTGTTCAT[A/G]TTTCCTAGCTGTACA	114804
rs572137296	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76206596	CCTGAGGTCAGGAGT[A/T]CGAGACCAGCCTGGA	114804
rs572154640	snp	A/T	0.000798403	0.0199641	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152589	GTTAAAAAAAAGACA[A/T]TAATTAAGCGGATAA	114804
rs572159122	snp	A/C	0.00478085	0.0486577	intron-variant	RNF157	GRCh38.p7	17:76227914	GTAGTGTCAGGTCCC[A/C]AAATCTAGCTATATT	114804
rs572165426	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76163537	CAAGGCCCAATCCCA[C/T]TCCCATTAACCTGGG	114804
rs572197208	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76195473	TTGAAAAGCGGTTAG[C/T]GGTATCTACTACAGC	114804
rs572209967	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76188261	TCCCACGGCCTCCTA[C/T]CTGGGATCACTCCAC	114804
rs572211839	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76164649	GAGAGAGCAAAAAGT[A/G]AAACAAAAATAAAAA	114804
rs572276597	in-del	-/CAG	0.00438332	0.0466095	intron-variant	RNF157	GRCh38.p7	17:76215874	GATACAGTGATACAA[-/CAG]CAGAATTCATCATTT	114804
rs572291698	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76196296	AGCAAATTGAACACA[A/G]TTCCACTTATATAAA	114804
rs572297287	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145486	CTCCGATGACGGTGC[A/G]AGCCACAGCACTCGT	114804
rs572345486	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76188947	AAGTCTATAATCCTG[A/G]TCTTTTGATATTTCA	114804
rs572354828	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76189954	CTCCTCCAGCCCTGT[A/C]GACCTTCCAGCACCT	114804
rs572374181	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76200645	CTGGAGACTGTACAA[C/T]GATGTGTGATGAGCA	114804
rs572375865	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157	GRCh38.p7	17:76156105	CTTGTCATGCAGTAC[A/G]GGTATTAGCTTGCCA	114804
rs572421537	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241489	ACATTTCAACTGCTA[A/G]AACATGACTTTCACA	114804
rs572458173	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76208153	GTTTTCAATTTCTAG[C/G]CTCAAGAGATCTATA	114804
rs572474749	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153886	ATAGTCCTCCCCCTC[C/T]CCCCAGTGGAAGAAA	114804
rs572490227	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76242150	GGGAACTGGTGTCCT[C/G]CTCCATACTCCTTTC	114804
rs572503689	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194881	TTAGCCAGGCGTGGT[A/G]GCGGGCGCCTGTAGT	114804
rs572583885	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151751	CTCTGACAACCTGAT[A/C]ACCTGTGAAGTTACA	114804
rs572587786	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76228508	TAACCATCCTTCTTG[C/T]TTAACACTTGCGTTC	114804
rs572603122	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76235022	ATCTATATGCTCTTC[A/G]TTGTGCCAATACCAC	114804
rs572614269	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76222705	AGAAACAGCAGAGAC[C/T]GAGAGATGCAAGGTT	114804
rs572663246	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144369	CTGGAGTGCATTGGC[A/G]CGATCTCGGCTCACT	114804
rs572678798	snp	A/C	0	0	intron-variant	RNF157	GRCh38.p7	17:76229072	AAAACTGTTCTCTGG[A/C]ACACCAACCAAACCA	114804
rs572795952	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76179399	ACCATCCCAAAAAGG[A/G]AAAAAAAAGAGGCCA	114804
rs572810549	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76238798	TATGCCTTGGTTAGC[A/G]TTGATTTTATGTAGT	114804
rs572878273	snp	A/C	0.0171132	0.090905	intron-variant	RNF157	GRCh38.p7	17:76239539	CTTTCCACCACCACC[A/C]CCCCCCCCACCCCCC	114804
rs572895783	snp	C/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76230625	TGGGTGGATCACGAG[C/G]TCAGGAGTTTGAGAC	114804
rs572902015	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76231218	TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCA	114804
rs573058895	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76219483	TTTAAAACAAGCAAT[A/G]TAAGGATAAATCATA	114804
rs573066061	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76226203	ACTGAGGGATCATGG[C/T]AACGTAAGCAGTGGA	114804
rs573067890	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76232548	ATTATGAGCAATGCC[A/G]CTATGAACATCTGCA	114804
rs573080397	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76226670	CTGGAGAACCCATGA[A/G]GTTTGAAGTGCTTGG	114804
rs573102830	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76175623	TTAGGCAGGAAAATC[C/T]GACACAAACGCTAGT	114804
rs573161977	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76224663	ACACTGGAAAAAGAA[A/G]AATGGTCTTACGCCA	114804
rs573174691	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146086	GCGCCTGTCTGGAAA[C/T]CCATTCTTGGTGCTT	114804
rs573231195	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76158682	CGATCCTCTTGTTGA[C/T]GCTTTAACAGAGGAG	114804
rs573239685	snp	C/T			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146599	AGTGGCCTCCCCTCA[C/T]GAGGCATCTCTGGCC	114804
rs573252419	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76225477	TTTTATACATATACA[A/C]ATATGTCCAGGTCTT	114804
rs573307042	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76228222	CACAGACTGAACAAC[A/G]GTAGCTTCACAGCAT	114804
rs573340596	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76172239	GGACTGCTTGAGCCC[A/G]GGAAGTTAAGGCTGC	114804
rs573353490	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76184424	CTTCCCTTCTCCTGA[C/G]ATACATAACGTGTCC	114804
rs573368397	snp	C/T	0.00318978	0.0398085	intron-variant	RNF157	GRCh38.p7	17:76221893	ACCTCCAAAACAGTA[C/T]GCTGAGACAAAGAAG	114804
rs573370246	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76177657	TTTCTAGGCCTGCCC[A/G]TGGATGCCCAGGGAC	114804
rs573378924	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76201208	AGAATATGAAGAGCC[A/G]GGCACAGTGGCTCAC	114804
rs573469463	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76197389	ACTATGAGCCTGGAT[A/G]TGGTGGCTCATGCCT	114804
rs573470609	in-del	-/A	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76188603	CAGATAATTCCCCCC[-/A]AAAGCAATGCATGCT	114804
rs573475275	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76166195	GCCTAGGCTGGTCTC[A/G]AACTCCTGACCTCAG	114804
rs573489539	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76166604	TAATCTCAGAAAGGG[C/T]GATACTGTCAAGAAG	114804
rs573539878	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76143429	CCAGGGTAAGGGAAG[C/T]TCCCTGTCACCTGCT	114804
rs573586551	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76221322	TTACCAAAGTAAGTA[A/G]CTTCAAATTTTAAAG	114804
rs573590063	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76205067	GCTGGGATTAGAGGC[C/G]TGAGCCACCATGCCC	114804
rs573649521	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212826	AGATCCTAGCACTAC[A/T]CTCCAGTCTGGGCGA	114804
rs573726220	snp	A/G	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76169578	CACCCGGCCTAGTTA[A/G]GTTTTTTTTTTTTTT	114804
rs573730884	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76206123	GTAGTCCCAGCTACT[A/G]GAGAATCTGAGGTGG	114804
rs573736198	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213709	CTGGAAAGAAAAGGC[A/T]GGATTAGAGGGTGGG	114804
rs573747658	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76160212	CTATTCTCCTAGTGC[C/T]GGGAATCTAGTTGTG	114804
rs573768960	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76206863	AGGTAGCAAGTATAG[C/T]TAACATTGCTGCATG	114804
rs573823798	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76211295	TCCTGGAAAGGCCTC[A/C]TCCAACCCACCATTC	114804
rs573923252	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76163395	AGACGGGGTTTCACC[A/C]TGTTGACCAGGCTGG	114804
rs573927588	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76242254	ACACAAGGCCTTCGA[A/C]ACATCACAGAGTAAA	114804
rs573943582	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76199978	CGCGGTGGCTCACGC[C/T]TGTAATCCCAGCACT	114804
rs573952784	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76200915	CTCTCCTCCTCCCCA[C/T]GCTTACTCTGGTTTT	114804
rs573957694	snp	C/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76211199	ACAGCGCCTATCACA[C/G]TACCTGACACGCAGT	114804
rs573958700	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76167948	CACAGAGTGCTTCAT[A/G]ACCCATGTTGCTGGG	114804
rs573961491	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76181609	TGGCGACTTCTTCAC[C/T]AAATTGTTTTCAAAA	114804
rs573990639	snp	C/G	0.00159617	0.0282053	intron-variant	RNF157	GRCh38.p7	17:76211828	ATTTATGAGAAGGAA[C/G]AAGTGAGAGAAATGT	114804
rs573999570	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76179586	TAGTCCCAGCTACTA[G/T]GGAGGCTGAGGCAGA	114804
rs574022052	snp	C/T	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76234013	GTCACAGCTCATTTC[C/T]CCCTCTCCTCAGCCT	114804
rs574065326	snp	A/C	0	0	intron-variant	RNF157	GRCh38.p7	17:76171432	GACCTCGGTGATCCG[A/C]CCGCCTTGGTCTCCC	114804
rs574125527	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76202518	GATGGGTCTTCAAAG[A/G]TTACAGCAATGATGC	114804
rs574164111	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76203386	CTTAACCAACATGAC[A/G]AAGTCAGTCAGTGGC	114804
rs574167104	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241224	ACATCCAGCCTCTGT[C/T]TGTATCGTGGAAACG	114804
rs574229879	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76160838	TATAATTTATTCTAG[A/G]TTTTGAATGTTTTGC	114804
rs574257590	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76187207	TTTTTTTCTTAAGAT[A/G]GAGTCTCGCTCTGTC	114804
rs574276962	snp	C/T	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76187799	GATAGGGTTTTACCA[C/T]GTTGGTCAGGCTGCT	114804
rs574301085	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76162242	CCTCCTATAAGGCCC[A/T]GAGCTGGGCCTCTCA	114804
rs574336165	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76197231	GCTGTATAATATCCA[A/G]GCGATTTTGATGTCT	114804
rs574349142	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76170528	ACCTTTCCAGGGAGA[A/G]TCATCTGCCTGCCTT	114804
rs574470497	snp	C/T	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151134	ACGCTCCCTCCTCCA[C/T]GCTCAGGCAGGAAGG	114804
rs574472373	snp	A/C/G	0.0158469	0.0875917	intron-variant	RNF157	GRCh38.p7	17:76157114	TGGGACTACAGGTGC[A/C/G]TGCCACCACACCTGG	114804
rs574511088	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151854	AACTGGTAACCCAAA[A/G]CTCACTGGATCACAG	114804
rs574541391	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76196616	GGGCCGAAGTATGTA[A/C/T]GGGAGTGTAGTCATG	114804
rs574563504	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146148	CACAGCCTCCTGTGG[A/G]CTCACTTCCTGGCCG	114804
rs574590561	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76190739	GATGAAACCCCGTCT[C/T]TACTAAAAACACAAA	114804
rs574599365	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76237960	GTGGTGGCAAACACC[A/T]GTAATCCCAGCTACT	114804
rs574606393	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76194801	TGGGCAGATCACGAG[A/G]TCAGGAGATCGAGAC	114804
rs574613126	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76182162	TAAGCCTGAATCTGA[A/G]AATAACTTAAATCCC	114804
rs574629068	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76183540	GACCATAGTGCACTA[C/T]AGCCTTGAACTACTG	114804
rs574708933	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76231286	ACAGGCGTGAGCCAC[C/T]GTGCCCGGCCTCTTG	114804
rs574763083	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76235456	GCCCGCCTCGGCCTC[C/T]CAAAGTGCTGGGATT	114804
rs574785725	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194888	GGCGTGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT	114804
rs574793693	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76144984	TGAACATCAATATAC[C/T]GTGAGGACATTCCAG	114804
rs574819316	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76189127	GTATCCTGGACTAGA[C/T]CCTAGAACTAAGAAA	114804
rs574843223	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76217404	TGAAATGAACCCCTC[A/T]AGCAGCTTGCTTTCA	114804
rs574870491	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147666	TGGCAAGGACCCTGA[A/G]GGGCCCACGGCAAAG	114804
rs574872275	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76154892	CACACAGGTCTGTAT[A/G]GGTCTATATGTGCCC	114804
rs574897219	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76189753	GAAGCCCGGAGAAGG[A/G]ACCCTCCGAAGCTGG	114804
rs574911799	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76235975	GATAACACCACTGCA[C/T]TCCAGCCTGGATGCC	114804
rs574933514	snp	A/C	0.00755907	0.0610114	intron-variant	RNF157	GRCh38.p7	17:76182829	TATATCCTATATATC[A/C]TATATATGATATATA	114804
rs575020026	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76229205	CTTGTTTCACTTTTC[A/C]CCATACAGATGGACA	114804
rs575094473	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76223428	CCTGACCTCAGGTGA[G/T]CCATCCGCCTCGGCC	114804
rs575116954	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76162888	AATAATAATACTTGC[A/G]CTGCAGCATACTATT	114804
rs575180457	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76174089	AATAAAAAAAAAAAC[C/T]GCTGAAGTTCCAAAT	114804
rs575222126	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76210254	TGGTATTTTGAAAAG[C/T]GTACTACTGGACGAA	114804
rs575228887	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76225708	CACAGCTACAGCAGA[C/T]ACTCTATGTACAAGC	114804
rs575243271	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76217376	CAACCAAAAATTTGC[C/T]TTTTCCTTTCTTTGA	114804
rs575276038	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76233144	CCAGGATGGTCTCGA[A/T]CTCCTGACCTCATGA	114804
rs575276818	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76186375	AGCTGGGCGTGGTGG[C/G]GGGTGCCTGTAATCC	114804
rs575303818	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76218116	AAATATCAAGAAAAA[A/C]AACCAAAAGGTATGA	114804
rs575306140	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76180015	ATAAAGTCTTTCTGA[C/T]GTAAGCATCCTGGCA	114804
rs575312972	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76179513	GCCTGGCCAACATAG[C/T]GAAACCCCATCTGTA	114804
rs575382593	snp	A/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150692	CTTTCCATAGCCCTT[A/G]CCACAGAAGCATTCC	114804
rs575423019	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76236102	TGGGCCTCTAGTCAG[C/T]TGAAGGCCTTAAAAG	114804
rs575447764	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76226780	CCCCACCAACACCTC[A/G]TTGCTCAGGAAGCTC	114804
rs575467340	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76211896	CAGTCATTCATTCAA[C/T]AATCATTTATTAAGG	114804
rs575501651	in-del	-/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76230291	AGCAACCAGCCGACA[-/T]TTAGGACTCACTTCA	114804
rs575504225	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76227122	CTCTTTTTTTGTTTT[G/T]TTTTTTTTTTGAGAC	114804
rs575561846	in-del	-/TTC	0.00318978	0.0398085	intron-variant	RNF157	GRCh38.p7	17:76187180	TAGGATTTTCTTTTT[-/TTC]TTCTTCTTTTTTTTT	114804
rs575582425	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76203982	CTGTGTTAGCCAGGA[A/T]GGTCTCGATCTCCTG	114804
rs575620888	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76210400	TCGAGACCATCCTGG[C/T]TAACACAGTGAAACC	114804
rs575631724	snp	C/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76221981	AGGTAAATCCACAGA[C/G]AGAGTAGACTGGTGA	114804
rs575643856	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76222505	AAGAATTTGGCACAG[G/T]CAGGTTATAATGCTG	114804
rs575669703	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76178287	AAGCTTCCGGGTGCC[A/T]CCACATTCCCTGGTG	114804
rs575684243	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76166292	ACCCACACTTTTCAC[A/G]TCAGCCCAGGAGCTT	114804
rs575704410	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76176010	TACACACACATACAC[A/G]CACAAGACAACAACG	114804
rs575766927	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76166681	CAAGTTTGTTAACTG[A/C]GGGCCATCAGCTGCT	114804
rs575816428	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76205848	CAGCTACAGAACACA[C/T]GAGAGGATACAGACT	114804
rs575891999	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76238979	GGGATGCGGGCAGGT[G/T]CATCGTCTGGCCCCT	114804
rs575928921	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76200462	GTGAAATAAGCCAGT[C/T]ACAAAAGAACAAATA	114804
rs575941838	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76214733	TTGCCCCTTCTTAAT[C/T]AGCCAGGAGGCAGAA	114804
rs575959854	snp	A/G	0.00358779	0.0422022	intron-variant	RNF157	GRCh38.p7	17:76229082	TCTGGAACACCAACC[A/G]AACCAAGTCTTGTCT	114804
rs575969954	snp	C/T	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151984	CGCAGGCAATCCTTC[C/T]AAGACCTTCGTAGAG	114804
rs575974711	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76160407	TTTTCTAGTTACACT[C/T]CTATAAGTAATACAG	114804
rs575977698	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76198264	AAAGTTGGATGAGGG[A/G]GAGCCTGTTGATACA	114804
rs576012137	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76192274	AGTTCAAGCACTTAG[C/T]GGCACTTTTCGAGTC	114804
rs576023106	in-del	-/CT			intron-variant	RNF157	GRCh38.p7	17:76192565	ATATGCCCATGGTGA[-/CT]CTTTAGATTTTGAAT	114804
rs576058615	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76175827	CCCTGCCGCAAAAGA[A/C/G]AGAAAAATAAAAAGA	114804
rs576060093	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76208354	GCAGCATGGTTCAGG[C/T]TCTGGAGCCAGACTG	114804
rs576078199	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76176302	TTCTGGCTGAGGTAA[C/T]CTGAAGGCTTCATGG	114804
rs576112953	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76163034	AAAGAGAAAGAAAAA[C/G]AAGAAGAAGTTGGCA	114804
rs576114520	snp	A/C			upstream-variant-2KB	RNF157	GRCh38.p7	17:76241910	TCGTATTTTTCATTG[A/C]CGTCTTTTCAGCAGC	114804
rs576134969	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194207	TACCCCCACATTCCC[C/T]TGTGCCCTCTCTAGT	114804
rs576194647	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76169691	TTCAAGTGATTCTCC[C/T]GTCTCAGCCTCCCAA	114804
rs576232073	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76189132	CTGGACTAGATCCTA[A/G]AACTAAGAAAGGACA	114804
rs576252983	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76202334	GGGGTAAGTGGTGGC[C/T]TCTCACAGAGGCTGT	114804
rs576332789	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76235490	GGCGTGAGCCACTGC[A/G]CCCAGCCGTAAATTG	114804
rs576372966	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76194918	TACTCAGGAGGCTGA[A/G]GCAGCAGAATGGCGT	114804
rs576375974	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76207000	GTTTGCCAAGGTTAC[A/G]AAGAGTTTAATGGTA	114804
rs576388489	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76207464	ATGGATTATCCTAAG[A/T]GGTAGATCTGTGGTG	114804
rs576391807	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76166077	CCTCCCAGGTTCAAA[C/T]GATTCTGCTGCCTCA	114804
rs576409258	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76195296	TTTTCCAGACACCAC[G/T]TAACCAGGAGATCAC	114804
rs576409584	snp	A/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76189292	AGGCTATATGGCAAC[A/T]CTGTTATCTTTTGTG	114804
rs576410861	snp	C/G			upstream-variant-2KB	RNF157	GRCh38.p7	17:76241134	CTATTCAAAGCGCTC[C/G]CAACTCTATACATGC	114804
rs576499018	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157	GRCh38.p7	17:76156065	GTAGGAAAGCAAGTC[C/T]TCTTCCCTCTCAAGC	114804
rs576508521	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76226428	TATTAGTCTCCTGGA[C/G]TAGGGGGGCAAAGAG	114804
rs576575178	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76184613	ATGATCTATATTAAC[G/T]GCAGTAAACCTCTTT	114804
rs576580719	snp	G/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76234905	ATCCCAGCATCATTT[G/T]TTGAAACCACTATCC	114804
rs576594844	snp	A/G	0.00993419	0.0697739	intron-variant	RNF157	GRCh38.p7	17:76181677	CTTTGGGAAGCCGAG[A/G]CAGGCAGATCACCTG	114804
rs576601371	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76227791	CTCAGGCAGGAGAAT[C/T]GCTTGAACCCGGGAG	114804
rs576651516	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76181156	TGCACTGCTTCTACT[A/G]TAGGGCAAGTCTACA	114804
rs576665083	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76184769	GAGAGTGTCACAGAT[A/G]ACCTTGCACACAAAA	114804
rs576665218	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76192098	GTGCACAATGACAAC[A/G]GGAAACAGAGGTGAG	114804
rs576677352	snp	C/G			intron-variant, upstream-variant-2KB, downstream-variant-500B	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142275	CAGGAGCTGGAGAGC[C/G]GGGGTCGGGGAGGCT	114804
rs576686314	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149994	GCCGAGATCGCGCCA[C/T]TGCACTCCAGGCTGG	114804
rs576700297	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76228420	TCAAGGAGGCATTCC[G/T]CCTTTCCAAGGTTAA	114804
rs576707790	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76185390	TTAAAAGGAGAAAAG[C/T]GTGCTCTTAATAAAG	114804
rs576711139	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76157688	TGCTATTCCCATGTA[C/T]ATGTCCTGTCCCAGC	114804
rs576728657	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76158297	TGACAAGGTGTTTGA[G/T]GAGTGAATGAGAGCA	114804
rs576760278	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144296	GAAATCATCTTAACT[G/T]GGGGATTCTCAGATT	114804
rs576772964	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76158667	ACTCCTGGGCTTCAG[C/G]GATCCTCTTGTTGAC	114804
rs576785572	snp	A/G	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76236127	TAAAAGCAAAAACCC[A/G]GGTTTAACCAAGCTA	114804
rs576792577	snp	C/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76196518	TTATACATCAATAAA[C/T]ATTTTTAAAGAGGAC	114804
rs576803813	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145086	CAGTTCCCTCTGAGA[A/G]GTGAGGGATTGTGGT	114804
rs576839455	snp	C/T	0.00199481	0.0315187	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145441	GCCCAGGAGCCGGCA[C/T]GGAAGGAGCAGGATG	114804
rs576893444	snp	C/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76210392	AGGTCAGATCGAGAC[C/G]ATCCTGGCTAACACA	114804
rs576967257	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76225782	TTCCCCCTTGCCTTG[C/T]GGACCTCTTCTATCA	114804
rs576974240	snp	A/G	0.00398564	0.0444627	intron-variant	RNF157	GRCh38.p7	17:76171094	AGACGGGGTTTCACT[A/G]TGTTAGCCAGGATGG	114804
rs576975541	snp	A/G	0.0126979	0.078662	intron-variant	RNF157	GRCh38.p7	17:76230473	AGTTCAATTACAATG[A/G]GTTATCTTCTAAGAG	114804
rs577037374	in-del	-/T	0.11228	0.208646	intron-variant	RNF157	GRCh38.p7	17:76204783	TTCTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTGA	114804
rs577043778	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76178325	GGAGAGCTGCTTGCA[G/T]TGCACCTGGTCCAGC	114804
rs577112399	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76171455	GGTCTCCCAAAGTGC[C/T]GGGATTACATGCATG	114804
rs577135083	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147527	TTCTATAGAAGCCTT[A/G]GCCAGGGCAGAACAT	114804
rs577162516	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76217213	TGGAGTTTCACCATG[C/T]TGGCCAGGCTGGTCT	114804
rs577204791	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, downstream-variant-500B	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76141992	TGATGAAGCAGAGCC[C/T]GTGGGTAAAACTCTG	114804
rs577232236	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76181779	TGGGTGTGGTGGCGT[A/G]TGCCTGTACTCCCAG	114804
rs577241654	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142924	TAGGCTGTGCCCTGT[A/G]GGAGAAGCCAGGCCC	114804
rs577247429	snp	G/T	0.00557542	0.0525036	intron-variant	RNF157	GRCh38.p7	17:76182857	ATAGGATATATAGGA[G/T]ATATATATCCTATAT	114804
rs577278216	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76194820	GGAGATCGAGACCAT[A/C]CTGGCTAACATGGTG	114804
rs577279119	snp	C/T	0.00478085	0.0486577	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76143271	AAGGACAGGGATCCT[C/T]AGGAAGGGGGTCCTG	114804
rs577280411	snp	C/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76177092	CACCGGGGGAACAGG[C/G]AGAGCTCATGGCGAT	114804
rs577284973	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76183337	AATCTGTATTTTAAT[A/C]AACATTCCAACCAAT	114804
rs577296568	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76222060	GTTTTATTTTGAGGT[G/T]ATAAAAATGTTCTAG	114804
rs577303210	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76230548	TCATATTTCTTAAAA[A/G]GAGATACTGAGCCGG	114804
rs577319453	snp	G/T	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76177560	GTGCTGAGGGCAGCT[G/T]GGTGCTGGCCTTCAG	114804
rs577353902	snp	C/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76189802	GAGGGTACTGCCCAG[C/G]TGGTTCTGGGTTTGT	114804
rs577366432	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76224579	TAATGCTACAGTGCT[A/G]CTTTTGTTCTTCATT	114804
rs577370352	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76168076	TTTAAATAGTTTCCT[A/C]AAGGCAAAAAACAGC	114804
rs577514118	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76215641	ACTGAACCAAACATT[A/C]ATTTTTAAAACTTTC	114804
rs577522669	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76216585	GGCTCTGTCTCTGTA[C/T]ATTTAAAAATAATAA	114804
rs577569797	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76227192	ATGACACGATCTTGG[C/T]TCACTGCAACCTCTG	114804
rs577585506	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76210307	AGATAGAAAGGAAGA[A/G]AACCCGCCGGGCGCA	114804
rs577604832	snp	A/C			upstream-variant-2KB	RNF157	GRCh38.p7	17:76240757	GCGGGGCGGGACCGG[A/C]CGGAGCTGGGACCCC	114804
rs577613862	snp	C/T	0.00119737	0.0244387	intron-variant	RNF157	GRCh38.p7	17:76218246	ATCGGTGTCATCAGA[C/T]TTTTCAACAGAAACA	114804
rs577626787	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76219433	TGTGTGTAAGGAAGA[A/G]TGGCTATGAAGATAT	114804
rs577626835	snp	A/G	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76210534	GGCAGAGCTTTCAGT[A/G]AGCCAAGATCGTGCC	114804
rs577647606	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76180149	TCAGTATGGATTTAT[A/G]GAATGGCTTCCTGTT	114804
rs577668331	snp	A/G	0.00597247	0.0543191	intron-variant	RNF157	GRCh38.p7	17:76181688	CGAGACAGGCAGATC[A/G]CCTGAGGTCCAGAGT	114804
rs577689964	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76211117	GCCCACCTTTCCAAT[C/T]GGGCCAGACTGGTTT	114804
rs577738668	snp	C/T	0.0023933	0.0345097	intron-variant	RNF157	GRCh38.p7	17:76221249	CATTACCAAACCTCT[C/T]CCCCACAAAAAAGAC	114804
rs577747534	in-del	-/AAATAAATAAAT	0.00478085	0.0486577	intron-variant	RNF157	GRCh38.p7	17:76186941	TGAGACTCCGACTCA[-/AAATAAATAAAT]AAATAAATAAATAAA	114804
rs577750911	snp	G/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76187091	GCCCTGGCAAGGTCT[G/T]GTTACTCTGGCTAGG	114804
rs577789965	snp	A/G	0.000798403	0.0199641	intron-variant	RNF157	GRCh38.p7	17:76187697	ATCCGGGGTTCAAGC[A/G]ACTCTCCTGCCTCAG	114804
rs577797632	in-del	-/G	0.00517822	0.0506191	intron-variant	RNF157	GRCh38.p7	17:76158335	CTGATGAGGCATGCA[-/G]GTAGGAGGGAAGTCC	114804
rs577834052	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76239722	GTGCCTGTTTGGATG[C/T]CGAGGTCGCCTCCCT	114804
rs577888298	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76211905	ATTCAACAATCATTT[A/C]TTAAGGGCTTAACAT	114804
rs577943555	snp	C/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76232684	TCCAACTTTCCAAAG[C/T]GGCTGTACTATTTTA	114804
rs577947380	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF157	GRCh38.p7	17:76240380	CGCTGCGGCTCTGGC[A/G]GCGGGGAGCCCCCGG	114804
rs577949292	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212765	TACTCAGGAAGCTGA[G/T]GCAGGAGGATGGCTT	114804
rs577958294	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150777	TCTTAGTACCCTGGA[C/T]ACAGGCCCTTGCCAA	114804
rs577980220	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213531	GCCAAGATCACACCA[C/T]TACACTCCAGCCTAG	114804
rs577997565	snp	A/C	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76205295	AGGTGTGTACCACCA[A/C]CCCTGGCTAATTTTT	114804
rs578032883	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76164178	GATGTCTCCTCCTAC[C/T]TCTACAAGAGTGGAA	114804
rs578072079	snp	G/T	0.00199481	0.0315187	intron-variant	RNF157	GRCh38.p7	17:76197967	CTCCCTTGAAGATGG[G/T]AGGAACCTGCTCCTC	114804
rs578115039	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76206013	GACAGGAAGACTACT[C/T]GAGCAAAGGAGTTTG	114804
rs578163969	snp	G/T	1.65157e-05	0.0028736	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159504	GAACTGCTGGGGACG[G/T]GGTGAGGGGCCCGTT	114804
rs578170878	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76196951	CTCATGTTTGGTTTT[A/G]CTCCACTGCCCCATC	114804
rs578229042	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76148403	TCCTGAGTAGCTGGG[A/G]CTACAGGCACTCGCC	114804
rs578250115	snp	C/T	0.000399281	0.0141238	intron-variant	RNF157	GRCh38.p7	17:76193620	TCGGTTTAGGATCAC[C/T]AGGGAAATGGAAGAC	114804
rs745312108	snp	A/G	0.000252851	0.0112411	intron-variant	RNF157	GRCh38.p7	17:76162009	TTCAGCCACCTGGCC[A/G]AGGAGAAAGAAATGT	114804
rs745347806	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76192437	TGAGGGCAAAATCCA[C/T]GTAGGAATCCTCTTC	114804
rs745352186	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76207288	ATTAGCCCAGTGTAG[C/T]AGCATGCACCTTTAT	114804
rs745378595	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76161744	CTCCCAGCGCGCATC[C/T]GTTTGTCAGATCCAG	114804
rs745451941	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76220072	AAAGGCCTAGAAACA[C/T]AGACCAACAAAGTAG	114804
rs745453541	snp	A/C	1.80292e-05	0.00300238	intron-variant	RNF157	GRCh38.p7	17:76162527	TCCTGGAAAGAGTAC[A/C]TTCAGAATTTTGGGT	114804
rs745466324	snp	C/T			intron-variant, missense	RNF157, RNF157-AS1	GRCh38.p7	17:76152229	AACTGGTCTCCAGCA[C/T]TAGCACACCCCAGGC	114804
rs745534263	snp	G/T			upstream-variant-2KB	RNF157	GRCh38.p7	17:76241441	TTTGTGGGTCTGGTG[G/T]TTTTTTTCCTGAGAG	114804
rs745550125	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76193711	GTCTAACAAACAAAC[A/G]TGACTTCTGAAGCCT	114804
rs745580195	snp	A/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151467	ACCCGTGATGTGGCT[A/G]TTCTGAAGCTGAAGT	114804
rs745583920	snp	G/T	1.65241e-05	0.00287433	intron-variant	RNF157	GRCh38.p7	17:76155215	AGCACTCCTCTGGTT[G/T]TGGGAAGGGGGCACC	114804
rs745584087	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76210496	TCAGGAGGCTGAGGC[A/G]GGAGAATGGCGTGAA	114804
rs745600111	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76232757	TCTCAACATTTGACA[C/T]TGTCTGCCTTTTCTA	114804
rs745613004	snp	C/T	3.29804e-05	0.00406068	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76159439	GCCATCACTGCCATA[C/T]GAAGGGAGCATTCCT	114804
rs745655491	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76191679	CTAGGAAGGCTGACG[C/T]GGGAGGACTGCTTGA	114804
rs745660491	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76155416	GTCAAATAGGAGGGT[C/G]AGACCTAAGGGAATG	114804
rs745669056	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76220673	TTTTTTTTTTTAGTT[A/C]GCTGGGCCAGGCGCA	114804
rs745676455	snp	A/C			utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142832	GGCTCTGTGAGGAAG[A/C]CGGGATCACACCACC	114804
rs745713250	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76231462	CCACCATGCCTGGCT[A/G]ATTTTTAAAATTTTT	114804
rs745735639	snp	A/T	1.65203e-05	0.002874	intron-variant, synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76155300	AAAGTTGCTGTCTGG[A/T]GACTCCGCTGGCAGC	114804
rs745803349	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76218751	CCAGCCTGTCCACCA[C/T]AGTGAAACTTCGTCT	114804
rs745825196	snp	A/C/G	6.59167e-05	0.00574061	missense, synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76167776	GGCCTCTTCTCCAGG[A/C/G]CTCTTCACTTCCTCA	114804
rs745834586	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76185397	GAGAAAAGCGTGCTC[C/T]TAATAAAGCAGACAC	114804
rs745851878	snp	A/G	4.94817e-05	0.00497377	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161869	ATGGGGCAGTTGTTG[A/G]CCTGGTAGCGCAGCG	114804
rs745876765	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76235075	TATAGTAATTATATG[C/T]ATAGTAACTTTTAAA	114804
rs745884070	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76222256	GAGGCTGAGGCACAA[C/G]AACAGCTTGAACCTG	114804
rs745907201	in-del	-/C			intron-variant	RNF157	GRCh38.p7	17:76228312	CAACCCTGTACCCTT[-/C]CTTCCTTGTGGTGCT	114804
rs745994048	snp	A/G	1.72308e-05	0.00293515	intron-variant	RNF157	GRCh38.p7	17:76155761	GGGGATGGGGAAAGG[A/G]GCCTGGAGGTCAGGC	114804
rs745995786	in-del	-/GAGAGGTGGCCATCTCCAAGCAC	1.64904e-05	0.00287139	frameshift-variant, nc-transcript-variant	RNF157	GRCh38.p7	17:76159454	GAAGGGAGCATTCCT[-/GAGAGGTGGCCATCTCCAAGCAC]GAGAGGTGGCCATCT	114804
rs746041855	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76164612	TTTTCTTCTTTGATT[A/G]AAAAAAAAAAAAGAG	114804
rs746098591	snp	A/G	1.69631e-05	0.00291226	intron-variant	RNF157	GRCh38.p7	17:76164708	AATAAAAGGAAGGAA[A/G]GACCCTAATACTAAC	114804
rs746106103	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76223639	GAATTGTAAATCAAA[A/C]CCCTTAGTCTCAAAA	114804
rs746108927	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149048	CATCAACTGAGATCT[C/T]CTTCCTTTATTCCTT	114804
rs746120825	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76176631	AGGGAGCAGACAGAC[A/C]GCCCCTCCACAGCTT	114804
rs746123082	snp	A/G	1.64738e-05	0.00286995	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF157	GRCh38.p7	17:76212397	CAGAAAGTTCAGATC[A/G]CTGTTCTCTCCAAAC	114804
rs746216343	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76168484	TCATCACAAATTCCA[A/C]CCCAAGCTCTCTGGG	114804
rs746220066	snp	A/G			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76214241	GGACACCCAGCTGGT[A/G]TCCTCTGCAGAACTG	114804
rs746220427	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76157262	TGAGCCTCCGCGCCC[A/G]GCCAGTCACACAGTC	114804
rs746271089	in-del	-/AAAT			intron-variant	RNF157	GRCh38.p7	17:76186941	TGAGACTCCGACTCA[-/AAAT]AAATAAATAAATAAA	114804
rs746273573	snp	A/T	1.67536e-05	0.00289423	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167010	CAGAGGCAGCTCACC[A/T]CCTCTTCGGCCCACT	114804
rs746284459	snp	C/T			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212852	GGCGACAGAGTGAGA[C/T]TCTGTTTCAAAAAAA	114804
rs746300494	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76202617	CAAAGCTTCCTTAAC[C/T]GTGAGCTATTAGAGC	114804
rs746396504	snp	A/T	3.29522e-05	0.00405894	intron-variant	RNF157	GRCh38.p7	17:76161531	GGTTCCGAGCCCAAC[A/T]TACTGGATGCTCTTC	114804
rs746412724	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76156629	GCTGTGACATGGGGA[C/T]ACCCCAGGTTTCCCC	114804
rs746416076	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76201756	GTGGTTGTGGACATA[C/T]TGCCATCTCAGTGGA	114804
rs746435667	snp	A/G	1.65031e-05	0.00287251	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76158427	GACGGTCTCTGAGAG[A/G]GCTGTGTCTCCGACT	114804
rs746486580	in-del	-/AAC			intron-variant	RNF157	GRCh38.p7	17:76184591	CCTGCTGTAGATCAG[-/AAC]AACAATGATCTATAT	114804
rs746526843	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76172542	GTTGCAGTGAGCCGA[A/G]ATCGCAGTGAGCCGA	114804
rs746575050	snp	A/G	1.65151e-05	0.00287355	synonymous-codon, intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152464	TGCGCACGTCCTCTG[A/G]CCTGTAACGGAGTTA	114804
rs746581145	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76217793	CTAGTAGATAAACTT[C/T]GAGTGTTTCATTATT	114804
rs746582694	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76192235	TGGTTTGTTAAGAAA[C/T]ATGGCATCAAACAAC	114804
rs746609797	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76161468	GCCACGTAGAGAAGC[A/G]TGAAAAGTTTAAAAA	114804
rs746621933	snp	A/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150760	TATTTTTTCTCATAA[A/G]CTCTTAGTACCCTGG	114804
rs746641245	snp	A/T	1.64773e-05	0.00287026	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154249	CAGGAAAGAAAGATA[A/T]CTAAAGGAAGTAAAG	114804
rs746709996	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76160535	ATATCATTGATTTTT[A/C]ATGTGGTTGAACTTT	114804
rs746718812	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76188005	TTGTTCCGTTTTGCA[C/T]TGCTAAGCTTCTAAG	114804
rs746740873	in-del	-/CTT			upstream-variant-2KB	RNF157	GRCh38.p7	17:76241415	ATTTGTGTTTTAAAC[-/CTT]CTATTTTCTTTGTGG	114804
rs746757111	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76229673	TTATCTGAAGAGCTG[A/G]CACCAGAACTCCTCT	114804
rs746772455	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76197126	CAGCCAGATGGCAAT[A/G]AGGACCCATCACTGA	114804
rs746797015	snp	C/T	1.64814e-05	0.00287061	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167780	TCTTCTCCAGGGCTC[C/T]TCACTTCCTCAGCAC	114804
rs746805615	in-del	-/T	6.62449e-05	0.00575483	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152505	GAGGGGCTGGCTGTG[-/T]TTTTTCTCTGCGTTG	114804
rs746814585	snp	A/G			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153822	GAGTCCTCTTTTACA[A/G]TAATGTTGACCATAT	114804
rs746850296	snp	C/T	3.71547e-05	0.00430998	intron-variant	RNF157	GRCh38.p7	17:76173681	GTGCCTGGGACCTGG[C/T]CCCAGCCTCTGGGAA	114804
rs746863882	snp	A/G	1.6916e-05	0.00290822	intron-variant	RNF157	GRCh38.p7	17:76162014	CCACCTGGCCAAGGA[A/G]AAAGAAATGTAGCCA	114804
rs746868718	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76171697	ACCTTAATTTTGACA[A/G]CCACCATGAAAGGTA	114804
rs746902450	in-del	-/TTTT	1.65729e-05	0.00287857	intron-variant	RNF157	GRCh38.p7	17:76161495	AAAAGCCAATGAGGC[-/TTTT]ATTTGCTTCAGAGGG	114804
rs746910820	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76184001	TTGAGACCAGCCTGG[C/T]CAGCATGGTGAAACC	114804
rs746967880	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76198405	TTGATTCCAAAACTG[C/T]CACAGAGATCTTTAG	114804
rs746968900	snp	A/T			intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76154692	TCCCTTAAGATCCCA[A/T]ACCCCATCCAGATCC	114804
rs747065366	snp	C/T			intron-variant, nc-transcript-variant	RNF157	GRCh38.p7	17:76156476	GCAGCTTCTCTCTTC[C/T]GTCCTCACTTCAGCC	114804
rs747071000	snp	A/G	2.2964e-05	0.00338843	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145208	GAATGCAGGGCAGGA[A/G]GGGAGCCCAAGTGCA	114804
rs747112291	snp	A/G			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213942	TGTGCCCCTTCTCAC[A/G]TAACCTCGCCCTATG	114804
rs747159714	snp	A/C			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151921	TTCCTCTCTGATCCT[A/C]GCTGAAACACATTTC	114804
rs747197542	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76175956	TATCAATGAGTTCAA[C/T]TGTTTATAAATCCAC	114804
rs747213888	snp	A/T			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146794	CAACACCTGACCCAT[A/T]GGAGGACCTGTTCAG	114804
rs747222485	snp	C/T	1.65018e-05	0.00287239	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159362	TTTTTGAGTTTGAGT[C/T]CCTGACTGCTGCTGT	114804
rs747253419	snp	A/T			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145643	GAACTTACCCTGGGA[A/T]CCACTTTTGTATTTT	114804
rs747255635	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76187624	TCTGAGACAGGTTCT[C/T]ACTCTGTCGCCCAGG	114804
rs747284780	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76224247	TTTAAGTTTTTGGGA[C/T]ATATTCCTAATACCA	114804
rs747284894	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76194778	CCCAGCACTTTGGGA[A/G]GCCAAGGTGGGCAGA	114804
rs747316008	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76157640	TAGTCATTGAACAAA[C/T]ACTTACTGAGCAACA	114804
rs747319748	snp	A/G	3.29495e-05	0.00405877	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161540	CCCAACTTACTGGAT[A/G]CTCTTCAGAGTCAGA	114804
rs747408318	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76204085	AAAAACTTCTTAATA[C/G]AATATTCATAGCTCT	114804
rs747417843	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76239206	GTAATTAATTAAAAT[A/G]AAACTACTTGCAATT	114804
rs747428995	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76206298	AGCCTCTAATAACTT[-/A]AGAGTTGGGCAGTAA	114804
rs747444288	snp	A/G	4.96381e-05	0.00498162	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161642	TCTGAAGCAGTGCCC[A/G]GAAGGCTGTGAAGGA	114804
rs747493863	snp	A/G	5.02021e-05	0.00500984	intron-variant, downstream-variant-500B	RNF157	GRCh38.p7	17:76156177	GCTGGGTAAGGGGGA[A/G]GGACATGCAGCCACT	114804
rs747501787	snp	C/T	1.67539e-05	0.00289425	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76155595	GGCCCTGCTGGCAGG[C/T]TGGGGGGAAGAGAGA	114804
rs747523794	snp	G/T	1.65206e-05	0.00287403	intron-variant	RNF157	GRCh38.p7	17:76212311	TATTTTTGTTACATT[G/T]TTTGAATTGGCCACT	114804
rs747552691	snp	A/G			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212812	AGTGCAGTGAGCCGA[A/G]ATCCTAGCACTACAC	114804
rs747568086	snp	C/T	3.29544e-05	0.00405908	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154268	AAGGAAGTAAAGGAC[C/T]AGATCTTTTACCACC	114804
rs747577422	in-del	-/AAAC			intron-variant	RNF157	GRCh38.p7	17:76216919	ACAAAAACAAAAAAC[-/AAAC]AAACAAACAAACAAA	114804
rs747654155	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76188284	CACTCCACTGCCCCA[C/T]GTGGTCACCCATCAC	114804
rs747696114	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76157599	CGTCTCTGTTTTGGG[C/T]ATACTTCTTTTTTAT	114804
rs747696869	snp	A/T	3.30994e-05	0.004068	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167121	CTGTTGTCTTTGGGA[A/T]TGTAGCTATTGATAC	114804
rs747703346	snp	C/T	6.59098e-05	0.00574026	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154359	GGCCCTGTGAGTCTA[C/T]GAAGCGGCAAAATGA	114804
rs747736345	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76229538	CAAACCTTTGTCTCT[A/G]ATCTTCAGCATTTCA	114804
rs747804014	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76202758	ACAAGTCACAACAAT[C/G]ATCATCAGCCCTGGG	114804
rs747823335	snp	A/G	1.6516e-05	0.00287362	intron-variant	RNF157	GRCh38.p7	17:76167624	TAATCTGGGAAGGAA[A/G]TGGCTCTCCTGGTCT	114804
rs747854832	snp	A/G	1.65952e-05	0.00288051	intron-variant	RNF157	GRCh38.p7	17:76161655	CCGGAAGGCTGTGAA[A/G]GAGAAAACAGGCAAT	114804
rs747863781	snp	C/T			intron-variant, upstream-variant-2KB, downstream-variant-500B	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142421	ATTAAAGAGTGCTGG[C/T]GAAAGTCAGACAGAA	114804
rs747864912	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76160835	ATCTATAATTTATTC[C/T]AGATTTTGAATGTTT	114804
rs747875818	snp	A/G	1.67195e-05	0.00289127	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76162572	AATCTTGTGTGTTGT[A/G]CTTGTTTTCAATTCC	114804
rs747882868	snp	C/T			upstream-variant-2KB	RNF157	GRCh38.p7	17:76242039	GCTTGGGTTACAGGG[C/T]AAGTCCCTGCCCCGG	114804
rs747894338	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76176609	ACGGCTGCTGCAGGG[G/T]GGTCGCAGGGAGCAG	114804
rs747904035	in-del	-/T	1.67781e-05	0.00289634	intron-variant	RNF157	GRCh38.p7	17:76161796	TTTGTAAATGTCCTC[-/T]TGTCCCCTCTCCCAC	114804
rs747917834	snp	A/C/T	0.000141665	0.00841522	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76173778	CTTGGGGAGGTGGGG[A/C/T]GGCGTAAGGAAACTG	114804
rs747971523	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76162762	CAAAGGCCTGGATAA[A/G]TAAAAGATGCTTTTA	114804
rs748000832	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76221973	ATCCAGATAGGTAAA[G/T]CCACAGAGAGAGTAG	114804
rs748002900	snp	A/G	3.41291e-05	0.00413079	intron-variant	RNF157	GRCh38.p7	17:76164691	AGAAGAAGAAAGGAA[A/G]GAATAAAAGGAAGGA	114804
rs748039419	snp	A/G			intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153729	ACAACAGCCTTTAAA[A/G]TACTTGCCTAAGCTG	114804
rs748043311	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76207723	CTCATGTGCTGACAC[A/C]CAAGATCTTTTGCTA	114804
rs748059378	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76196717	CAAACAGCCATAGCT[A/G]CCCCTTCTCCAAGAA	114804
rs748066640	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76195575	ATGTAATAATAGAAC[A/G]TTCATAGCAGCACTA	114804
rs748089134	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76164450	AATAAATCTTGTTCT[C/T]TCATTTCTCAAGTCC	114804
rs748174557	snp	A/G	5.71303e-05	0.00534433	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145398	GCCAGACCTTTGGCC[A/G]AATCCAGATGGTGTC	114804
rs748196785	snp	C/T	1.6492e-05	0.00287154	intron-variant	RNF157	GRCh38.p7	17:76165584	GTGAAGAAGCCCAAA[C/T]AGCACATCTTGATGC	114804
rs748220343	snp	A/G			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212661	GAGATAAGGAGTTCG[A/G]GACCAGCCTGGCCAA	114804
rs748233528	snp	C/T			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153804	GTACGTCTGCCGGCC[C/T]GAGAGTCCTCTTTTA	114804
rs748302280	snp	A/C	1.64901e-05	0.00287137	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159458	GGGAGCATTCCTGAG[A/C]GGTGGCCATCTCCAA	114804
rs748335342	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76185798	CACACGAGCAACCCA[A/T]CCTCACTACCTCACT	114804
rs748350057	in-del	-/G			intron-variant	RNF157	GRCh38.p7	17:76197605	ATAGGGTCTCAATAT[-/G]GTACCCAGGCTTGGA	114804
rs748355003	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76199976	GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	114804
rs748357353	snp	C/G	1.65778e-05	0.002879	intron-variant	RNF157	GRCh38.p7	17:76155321	CGCTGGCAGCCCCTG[C/G]AGAAGAGCACAGTTT	114804
rs748365960	snp	A/G	1.66799e-05	0.00288785	intron-variant, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156335	TCCTGGGGGTTGTGG[A/G]GGGACACAACAGGAC	114804
rs748371984	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76206790	AAAAAACAAACAAAG[A/G]AAACAGTGAAGAACC	114804
rs748391562	snp	C/T	1.6671e-05	0.00288708	intron-variant	RNF157	GRCh38.p7	17:76161828	CACCAGTCCCCCTGC[C/T]GCTCTGGGGCTTACG	114804
rs748409438	in-del	-/CTT			intron-variant	RNF157	GRCh38.p7	17:76168964	TTCCAACTGTTGATC[-/CTT]CTTCTTCTGAAAGCT	114804
rs748435730	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76199724	GTGACGCAGCTCGCT[A/G]GTCTCCATCCTACTG	114804
rs748469219	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149596	CAGAGAGTTCTCCAG[C/T]AAATTTTCTGCCAGT	114804
rs748478522	snp	C/G/T	3.33174e-05	0.00408139	intron-variant, downstream-variant-500B	RNF157	GRCh38.p7	17:76156193	GGACATGCAGCCACT[C/G/T]CCCGCTCCTTATGTA	114804
rs748505810	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76209828	GCAGTGGAATGATCT[C/T]GGCTTACTGCAACCT	114804
rs748506266	snp	C/T	1.64838e-05	0.00287083	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	RNF157	GRCh38.p7	17:76212442	ATGAGTTGAGTCAAA[C/T]TTCTCTCCTCCCATA	114804
rs748512256	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76236549	GAACCGTGCTCTAAA[C/T]TGCTTTCTATGCTAA	114804
rs748518588	snp	A/G	1.65141e-05	0.00287346	missense, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156257	GTCCCTGTGCAAGAC[A/G]ACTGGTCAATAGCTC	114804
rs748527370	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76160375	TGCTGTTTTCTGCTG[G/T]TTTTTTTTTCAGTGC	114804
rs748622015	snp	C/T	5.99706e-05	0.00547556	missense, intron-variant, utr-variant-3-prime, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145308	GATGACAAGCGCCGG[C/T]GCTGGGCATTCCGAC	114804
rs748637240	snp	A/G	1.76896e-05	0.00297397	intron-variant	RNF157	GRCh38.p7	17:76164834	TGACAAGGAAGGGAG[A/G]GTAATAAAGCACCAG	114804
rs748642940	in-del	-/ATTA			intron-variant	RNF157	GRCh38.p7	17:76204235	TTCCTTGTATTGCTT[-/ATTA]ATTAATTCTGCCTCA	114804
rs748657318	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76222341	GACAGAGCAAGACCC[C/T]GTCTCAAAAAAAAAA	114804
rs748682388	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76225504	TCTTCCTGTTCTATT[A/T]TTTTTTTTAATTGAA	114804
rs748724103	snp	A/C/G	9.45682e-05	0.00687582	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76240157	CCCGCCCTCACCGGA[A/C/G]TTGGGCGGGTAGCGG	114804
rs748748162	snp	A/T	1.64912e-05	0.00287147	intron-variant	RNF157	GRCh38.p7	17:76167645	CTCCTGGTCTCCTGA[A/T]CTTACCTGGCAATAC	114804
rs748782840	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76179710	AACAAAAAATAAGTA[C/T]CTTATTTCAACCTAA	114804
rs748793192	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76227807	GCTTGAACCCGGGAG[A/G]CAGAGGTTGCGGTGA	114804
rs748838313	snp	C/T	3.3065e-05	0.00406588	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152487	CGGAGTTAATGCAGT[C/T]AGAGAGGGGCTGGCT	114804
rs748872510	snp	C/T	1.65833e-05	0.00287948	splice-donor-variant	RNF157	GRCh38.p7	17:76161842	CCGCTCTGGGGCTTA[C/T]GCAGTCGGCAGATGG	114804
rs748877404	snp	A/G			upstream-variant-2KB	RNF157	GRCh38.p7	17:76241819	TCACCATGCTGGCCA[A/G]ACTGGTCTCCAATTC	114804
rs748880751	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76165381	CAACCTCTTTCACCA[C/T]TATAGCCTCTAAAGC	114804
rs748887594	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76208485	GAGGACAAAATGAGA[C/G]AACACAGATGAAAAG	114804
rs748908756	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76229407	AAAATAGAGACAATA[A/T]TACTTCTTTCAACAG	114804
rs748944783	snp	C/T	1.65149e-05	0.00287353	missense, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156267	AAGACGACTGGTCAA[C/T]AGCTCCAGATGACGA	114804
rs748953577	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76214766	ATTTTCAGTGCAATA[C/T]AATAACCAAATGAAA	114804
rs748972693	snp	C/T	0.000265609	0.011521	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161983	TCGGCACTGTTATCA[C/T]TCACTTCGTCTTCAG	114804
rs748986131	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76206566	GCACTTTGGGAGGCC[A/G]AGGTGGGTGGATTGC	114804
rs748990335	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76236870	GCAAACAGAGCAAGG[C/T]GTAGAACAGTCTAAT	114804
rs749014420	snp	A/G	1.65619e-05	0.00287762	intron-variant	RNF157	GRCh38.p7	17:76158508	GAAGTGGATCTGTAG[A/G]AGTCCAGTGGAAAAG	114804
rs749054915	snp	C/T	0.000239185	0.0109332	intron-variant	RNF157	GRCh38.p7	17:76164817	TGAAAATATGAAAGT[C/T]ATGACAAGGAAGGGA	114804
rs749067776	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76174403	ATTTACCATCCGCTT[C/T]TTCCCCCTTTGCCCG	114804
rs749123954	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76233681	AGCTGATATCATGCC[A/G]CCATGCCCAGGTAAT	114804
rs749148183	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76218865	CTTGAACCCGGGAAG[C/T]GGAGGTTGCAGTGGG	114804
rs749191029	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76207591	TAATATAACAATTCA[C/T]TTTAACATATTTCAC	114804
rs749205691	snp	A/G	1.64825e-05	0.00287071	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154365	GTGAGTCTATGAAGC[A/G]GCAAAATGAGTAAAC	114804
rs749267758	snp	C/T	9.9341e-05	0.00704703	intron-variant	RNF157	GRCh38.p7	17:76167134	GAATGTAGCTATTGA[C/T]ACAAGTGGGAGGCAA	114804
rs749277854	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76191408	ATGAGGTCAGGAGTT[A/T]AAGACCAGCCTGGCC	114804
rs749290646	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76166922	CTTCAAGCATCCGAG[-/T]CAGCCCCTTTGCTGT	114804
rs749313595	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76177582	GGCCTTCAGGGAGGA[C/T]GTGAAGGCTGGGGGC	114804
rs749334804	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76225381	AAAAAATTAGTATAT[A/T]TAAGTTAATAATTTA	114804
rs749411589	in-del	-/AA			intron-variant	RNF157	GRCh38.p7	17:76220387	TCGTAATGATATCTA[-/AA]AAAAAAAAAAAAAAA	114804
rs749433492	snp	A/G	1.68173e-05	0.00289972	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76155577	CTCTCCTTCTTCTGA[A/G]GGGGCCCTGCTGGCA	114804
rs749444099	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76224293	TTGAGCAATGGGTTC[A/C]CTAAATTATGTCTGC	114804
rs749468412	snp	C/T			intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76154876	TAGGCAGAAACCTCA[C/T]CACACAGGTCTGTAT	114804
rs749470661	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76166953	CAGACCGAGTCCTAA[A/G]TAGCCCCTAGGCCCT	114804
rs749480133	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76197285	CAGTTACAGTAAGGA[C/T]TGTGAAACTGGGTGA	114804
rs749486875	snp	C/G	1.75437e-05	0.00296168	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155650	GGGGCGATGTAGGAG[C/G]CAGACATGGAGGAGA	114804
rs749500589	snp	A/G	2.5363e-05	0.00356102	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76173714	TACTTGACGAGCCTC[A/G]GTGTGTCCTTTCGGA	114804
rs749608947	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76158172	GGACTTTTGTAGTGT[C/T]CCAGCTACTATCCTC	114804
rs749621268	snp	C/T	3.83597e-05	0.00437931	missense, intron-variant, utr-variant-3-prime, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145317	CGCCGGCGCTGGGCA[C/T]TCCGACTGACGGCAT	114804
rs749628971	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76234925	AACCACTATCCTTTC[C/T]CCATTCAATTGTCTC	114804
rs749634575	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76202724	CATAGTACCAAAAAG[C/T]GGCCAATCGAGGCTT	114804
rs749642516	snp	C/T	7.70475e-05	0.00620627	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76240170	GACTTGGGCGGGTAG[C/T]GGTACACGGAATTAG	114804
rs749676411	snp	A/G	0.000146402	0.00855451	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147347	AGCAAATGGTAAACA[A/G]GAGAGAAGACACACA	114804
rs749702535	in-del	-/CTT			intron-variant	RNF157	GRCh38.p7	17:76204075	CCCAGCCCATAAAAA[-/CTT]CTTAATACAATATTC	114804
rs749702822	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76189962	GCCCTGTAGACCTTC[C/T]AGCACCTCCCACTGG	114804
rs749720446	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76215967	ATAATTTATGGAGAG[A/G]GGAGGTACCTAGTTG	114804
rs749734105	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76176744	GCAAAGAGGAGCCCC[A/G]AGGCGGAGCTGGGCC	114804
rs749822162	snp	A/C	1.65034e-05	0.00287253	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76166503	CCACTAGAGGGTAAA[A/C]TTCTCGGTCTAAATC	114804
rs749827401	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76203770	AAAAAGTTTTGTTGC[C/T]TTTTTTTTTTTTTTT	114804
rs749834548	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76188836	TAAACCTGTACCACC[C/T]GGACCATGTAAACAG	114804
rs749839766	snp	C/T			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147101	CCTGGGGGTGGGTAC[C/T]GGAGCCTGGGACATG	114804
rs749846791	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76158955	CAGAAACCTTGTCAT[A/G]ATTTGTGCCTAGCTG	114804
rs749858018	in-del	-/CCCATC			intron-variant	RNF157	GRCh38.p7	17:76226609	GGAGGGACTGACCAA[-/CCCATC]CACAGTCAGCCATTC	114804
rs749897259	snp	C/T	5.00973e-05	0.00500461	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155615	GGGAAGAGAGAGCCT[C/T]TCCCTCCTCTTCAGT	114804
rs749940045	in-del	-/TC			intron-variant	RNF157	GRCh38.p7	17:76202112	AACCCAATCTCAGTT[-/TC]TCTCTCTCTCTCTCT	114804
rs749971691	snp	G/T	2.26585e-05	0.00336582	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76173760	TCAGAGTCTTCACGG[G/T]TTCTTGGGGAGGTGG	114804
rs749976993	in-del	-/GCTCCACCT			cds-indel, nc-transcript-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76144961	AGCCCATGGACCCCA[-/GCTCCACCT]GAACATCAATATACC	114804
rs750024712	snp	A/G	1.64727e-05	0.00286986	intron-variant	RNF157	GRCh38.p7	17:76162641	GAACAGCAAACAGAA[A/G]GGTTCAAGGACAGGC	114804
rs750043580	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76209265	GCCTCAACTTTAAGG[C/T]TAAGGCTGCTACCTA	114804
rs750052458	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76239726	CTGTTTGGATGCCGA[G/T]GTCGCCTCCCTCGCG	114804
rs750091733	snp	A/G	1.66338e-05	0.00288386	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76162618	GAGGTAGCTGACCCC[A/G]TCTACCTGAACAGCA	114804
rs750157154	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76199336	ATCACAGCTCACTGT[A/G]GCCTCAACCTCACAG	114804
rs750245340	snp	G/T	1.6563e-05	0.00287771	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159536	AGGGCCTCCAGAAGA[G/T]ATACTACTTCATAGC	114804
rs750250092	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76167520	AGTGGATAAGACATG[G/T]ACTCTCCCTATCTGG	114804
rs750294951	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76187416	GTCTTGAACTCCTGA[C/G]CTTGTGATCCACCCA	114804
rs750305197	snp	C/G/T			intron-variant	RNF157	GRCh38.p7	17:76226997	CTGCTGCCCCTAATA[C/G/T]GCCATGGTGGCCGTG	114804
rs750340657	snp	G/T	1.65817e-05	0.00287933	intron-variant	RNF157	GRCh38.p7	17:76161490	GTTTAAAAAAGCCAA[G/T]GAGGCATTTGCTTCA	114804
rs750358438	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76157256	CAGGCGTGAGCCTCC[A/G]CGCCCGGCCAGTCAC	114804
rs750367987	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76196397	GGGGAGCTTCTGGGG[G/T]TGCTGGCCATGTGCT	114804
rs750387858	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76233463	GAACTCTTCGCCCAA[A/T]CCAAATCAAATAACA	114804
rs750434482	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76200659	ACGATGTGTGATGAG[C/T]AGGGTGGTCACCCCT	114804
rs750438319	in-del	-/TAA			intron-variant	RNF157	GRCh38.p7	17:76236918	TTACACAAGAAACTC[-/TAA]TAAAAGAATTCCAAA	114804
rs750444675	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76169004	GGTCCTCTTTCTCAG[C/T]CACTGTGTGGGCACT	114804
rs750446481	snp	C/G/T	9.91699e-05	0.00704109	missense, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156225	CTTCTGGGGAGGAAA[C/G/T]AGTGGATGACAGAGG	114804
rs750471999	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76218378	AAGCCCAGTGGCTCA[C/T]GCCTGCAATCCCAGT	114804
rs750487019	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76203263	CCCAAAATGCTGCGA[C/T]TACAGGCGTCAGCCA	114804
rs750502523	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76158890	AACCACTGCCATTTA[C/G]AGGGTCTCAATATTT	114804
rs750504173	in-del	-/G			intron-variant	RNF157	GRCh38.p7	17:76236087	CTTGATTATGTGGGT[-/G]GGGCCTCTAGTCAGT	114804
rs750547039	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76191703	TGCTTGAGCCTGGGA[A/G]GTTGAAACTACAATG	114804
rs750561731	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76217075	ATAATTCTTTAGCAA[C/T]ATTAATTTCTAAACT	114804
rs750614388	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76237350	CAGTGCAGGTCTAGC[C/T]GCTTTCCAGCGAGCC	114804
rs750627990	snp	A/G	1.65217e-05	0.00287412	missense, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156236	GAAATAGTGGATGAC[A/G]GAGGCGTCCCTGTGC	114804
rs750684434	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76189864	GGCTGAAACAAACTG[C/T]AGCTGGTGGGATGAA	114804
rs750698567	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76159955	TCAATCTGTAAATAA[C/T]AATTTTATATTCTGC	114804
rs750744135	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76190691	TTGGGAGGCCGAGAC[A/G]GGTGGATCACGAGGT	114804
rs750762502	snp	C/G/T	4.99932e-05	0.00499945	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76164776	TTGAGGGGCTTGACA[C/G/T]AGAAAGTTCCATCTG	114804
rs750763659	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76229050	CAATAGTTTCCACCC[A/C]TCTACTAAAACTGTT	114804
rs750828775	snp	A/G	1.66062e-05	0.00288146	intron-variant	RNF157	GRCh38.p7	17:76159295	TGAAGCATTTCATCA[A/G]GGATTCCGGGGGCAA	114804
rs750830971	snp	C/T	6.59174e-05	0.00574059	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154232	ACCCCTTAAAGAATA[C/T]CCAGGAAAGAAAGAT	114804
rs750872584	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76193106	TTACAGGCGTGGGCC[A/G]GAGCACTCAGCCTTC	114804
rs750892922	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76182630	TAAATTATTAGGCAA[C/T]TCCCAGTAGTCTACA	114804
rs750936233	in-del	-/TAAG			intron-variant	RNF157	GRCh38.p7	17:76162093	GCTGAAGAGCTAAGA[-/TAAG]TAATAATTACGAACA	114804
rs750951948	snp	C/T	1.65392e-05	0.00287564	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167079	TGACACACTCCTCGC[C/T]TGTACTGCACAGTCT	114804
rs750961660	snp	A/G			intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154115	TCATAGAGATCATCA[A/G]TGCTCTGCTTGCTTT	114804
rs751041051	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76155836	TTCAGGCATTGAGGA[A/G]TGAAGTGGCCGTATC	114804
rs751066873	snp	A/C/T			intron-variant	RNF157	GRCh38.p7	17:76200868	AAAGGTGAATTACTG[A/C/T]ATGTTGGCACCAAGA	114804
rs751091973	snp	A/G			utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76143637	TCTCCATCAGGGCAG[A/G]ATGTGAGCCACAACC	114804
rs751173397	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76175110	TGTCCACCTCTATAT[C/T]TATGTGCTGTTTCAC	114804
rs751178761	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76232342	GCAGGGAGCTATGAT[C/T]GCACCACTGCACTCC	114804
rs751184233	snp	A/G			intron-variant, nc-transcript-variant, missense	RNF157, RNF157-AS1	GRCh38.p7	17:76147300	ATGGGGCAGGACTCC[A/G]GAGCTGCGGCTGTTC	114804
rs751197127	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76221096	ACTGCACTCCAGCCT[A/G]GGCAACAGAGACCCT	114804
rs751198077	snp	A/G			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146225	GTTTACAGCAGTGTG[A/G]CCTTGGGCACATCAG	114804
rs751299110	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76225683	CCCTACAAAATAATT[C/T]ATTGGAACACACAGC	114804
rs751337136	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76226198	TATGCACTGAGGGAT[C/G]ATGGCAACGTAAGCA	114804
rs751360413	snp	C/T	3.29924e-05	0.00406142	intron-variant	RNF157	GRCh38.p7	17:76161513	TTGCTTCAGAGGGGC[C/T]GTGGTTCCGAGCCCA	114804
rs751366406	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76225240	ACTGTAATCCCAGCA[A/C]TTTGGGAGGCTGAGG	114804
rs751409766	snp	A/G	1.70717e-05	0.00292157	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76155640	TTCAGTGCCAGGGGC[A/G]ATGTAGGAGCCAGAC	114804
rs751437019	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76199641	ATAGGTATAAACACT[A/G]ATTCAACTTCTCTGG	114804
rs751458666	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76238628	CACTATTGAAAATTC[C/T]AAGCTCAGCAAAGTA	114804
rs751501887	snp	A/G/T			intron-variant	RNF157	GRCh38.p7	17:76167410	GGCACAATTTGAAGG[A/G/T]AAAAGGTAAAGGGTA	114804
rs751534417	snp	C/T	3.28326e-05	0.00405157	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76155715	CATGACAGACTGGGC[C/T]AAGCTGCTGCTGGCA	114804
rs751550375	snp	A/C	1.64798e-05	0.00287047	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161933	GACAGGGCAGAATCA[A/C]GGTGTCCCGGACATC	114804
rs751583315	in-del	-/T	1.65985e-05	0.00288079	intron-variant	RNF157	GRCh38.p7	17:76167829	TCAGCATTTGCAGAG[-/T]AGCATATCAATATTT	114804
rs751595990	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76179197	TTAGGAGTTTTGAGA[C/T]CAGCCTGGGCAACAT	114804
rs751651814	snp	C/G	1.66696e-05	0.00288696	intron-variant, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156333	ATTCCTGGGGGTTGT[C/G]GGGGGACACAACAGG	114804
rs751661250	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76183450	TAAATTCACATAAAG[-/T]TTTTTTTTTGTTTTG	114804
rs751688203	in-del	-/CA			intron-variant	RNF157	GRCh38.p7	17:76179902	TTCTCAGTTCATATC[-/CA]CAGAGTTTCTGTTTT	114804
rs751691550	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76158766	AACCCAAATCTTAAG[C/T]AGGACTAGGGAAATA	114804
rs751717837	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76228683	ATCCCAGCACTTTGG[A/G]AGGCTGAGGCAGATG	114804
rs751725243	snp	A/G	7.94565e-05	0.00630253	intron-variant	RNF157	GRCh38.p7	17:76240137	CCTCGCGGCTGCGGC[A/G]CCCGCCCGCCCTCAC	114804
rs751761926	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76188355	ATCCTTCATCACCTC[C/T]AATTTTCCTTATTCT	114804
rs751761930	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76203060	CAGTGGCATGATCTC[C/T]GCTCGCTGCAACCTC	114804
rs751774485	snp	C/T	3.71492e-05	0.00430966	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145375	AAGAGAAAATGAACA[C/T]TACAGGAGCCAGACC	114804
rs751825838	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76171217	TTTTTTAGTTGGAGT[C/G]TCACTCTGTCACCCA	114804
rs751849627	snp	A/G	1.72184e-05	0.00293409	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76240232	CTGCCGGCTCGTCAG[A/G]GCCCCCATGGCCGCT	114804
rs751902025	snp	A/G	3.29837e-05	0.00406088	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159398	AGGCGGTCAAGAGGC[A/G]AGATCGTCCTGACGG	114804
rs751913657	in-del	-/C			intron-variant	RNF157	GRCh38.p7	17:76235109	GGTAGCGATAGTCCT[-/C]CCAACTTTGTTCCTT	114804
rs751949547	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76195109	TGACAAGTGGAAAGC[A/G]ATTCAGGAGAACAGA	114804
rs751954703	snp	C/G	1.6504e-05	0.00287258	intron-variant	RNF157	GRCh38.p7	17:76155245	CACTCCGTGCTGTTG[C/G]GGTTACCTCTGCATC	114804
rs751984563	snp	A/T	1.64738e-05	0.00286995	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167737	AAAGGTGAACTCAAC[A/T]TTGTAGTGGACTTTA	114804
rs752010854	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76227535	TCATTTTATAGAAGA[A/G]GAAACTAATGCACAG	114804
rs752016290	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76236265	AGGGAAACAAACTAG[A/C]TTTATGAGGTACTGC	114804
rs752016424	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76180649	AGGCTGGTCTCAAAC[C/T]CTTGAGTTCAAGTGA	114804
rs752023954	snp	G/T	1.65943e-05	0.00288043	intron-variant	RNF157	GRCh38.p7	17:76167178	ATCCGGCACAGATGG[G/T]TCTGACAACTTCCTC	114804
rs752036651	snp	A/C	0.000168095	0.00916621	intron-variant	RNF157	GRCh38.p7	17:76161810	CTTGTCCCCTCTCCC[A/C]CCCACCAGTCCCCCT	114804
rs752042090	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76196074	AACCTGCTCTGAGCC[A/G]CTACTCTCAACACAC	114804
rs752060110	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76163491	TGAGCCATCAAGCCC[A/G]GCCAGCCCTGTTTCT	114804
rs752143800	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76198254	GTTGGAATACAAAGT[C/T]GGATGAGGGAGAGCC	114804
rs752144319	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76209463	TAAACTTTCTTAAAA[C/T]ATTGTAAGATTTTTT	114804
rs752159400	snp	A/G	1.65946e-05	0.00288046	intron-variant	RNF157	GRCh38.p7	17:76159306	ATCAAGGATTCCGGG[A/G]GCAACAGTGTGGAGC	114804
rs752247774	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76216860	TGCGCCATTACATTC[C/T]AGTCTGGGTAAAAGA	114804
rs752314903	snp	C/G			utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76143564	AGAACATTAGGTGGG[C/G]CCTGAAATGGTAAAG	114804
rs752334213	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76183538	GTGACCATAGTGCAC[C/T]ACAGCCTTGAACTAC	114804
rs752348897	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76185109	TATGTTTTAGGTCTT[C/G]ACTCATTGTTTGAGA	114804
rs752396199	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76199345	ACTGTGGCCTCAACC[-/T]TCACAGGCTCAAGTG	114804
rs752503395	snp	A/G	1.68185e-05	0.00289982	intron-variant	RNF157	GRCh38.p7	17:76155746	GGGCCTTTGGAGACA[A/G]GGGATGGGGAAAGGA	114804
rs752509884	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76205508	GAGATGGGTAGATCA[C/T]GAGGTCAAGATATTG	114804
rs752512352	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76237040	TGTACACGTTTTCAT[C/T]CTTTTAAAGTTTGAA	114804
rs752523629	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76189665	ACGGAGCTGACAGAG[A/G]GAAACTGCAGGAAAC	114804
rs752572451	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76210715	AAAAAAGCAATTTCT[C/T]CAGGTCACTCACCTA	114804
rs752606884	snp	C/T	1.68309e-05	0.00290089	splice-acceptor-variant	RNF157	GRCh38.p7	17:76164797	GTTCCATCTGTGTGC[C/T]GGAATGAAAATATGA	114804
rs752643328	snp	A/C	1.6489e-05	0.00287128	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76165508	GTCACTCACCTTCTC[A/C]AAAGTACCCAGCAGT	114804
rs752657719	snp	A/T	3.54912e-05	0.0042124	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212524	AAACAAGCAGAAAAC[A/T]GTCAACCTAAATCTA	114804
rs752665251	snp	A/C	0.000174181	0.00933059	utr-variant-5-prime, nc-transcript-variant	RNF157	GRCh38.p7	17:76240243	TCAGGGCCCCCATGG[A/C]CGCTGCGGCTGCAGC	114804
rs752680944	snp	A/T	4.53669e-05	0.0047625	missense, intron-variant, utr-variant-3-prime, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145267	CCCACACACAGGGCC[A/T]CGTCTCAGAGTCCTC	114804
rs752695796	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76187387	ATGGGGGTTTCATCA[C/T]GTTGGCCAGGCTGGT	114804
rs752758041	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76194737	ACCACAAGAGCAGGC[C/T]GGGCACGGTGGCTCA	114804
rs752770592	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76179485	TCACTTGAGGTCAGG[A/G]GCTTTGAGACCGGCC	114804
rs752774588	snp	C/G/T	3.29724e-05	0.00406021	missense, intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152430	AGTCATTGTTATTGT[C/G/T]ACACTCCATACCTAG	114804
rs752783787	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76156562	GCCCAGGGCACAGCA[G/T]CTGCTGCGGCCATAC	114804
rs752783927	snp	C/G	1.64974e-05	0.00287201	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76166496	GCATGTACCACTAGA[C/G]GGTAAACTTCTCGGT	114804
rs752802424	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76200956	CCGCAAGCCCCCAGA[A/C]ACTTCCTGGCACACA	114804
rs752817960	in-del	-/C			intron-variant	RNF157	GRCh38.p7	17:76164114	ATGACCTGCCCCTCA[-/C]CCACCCTCCCTTGCC	114804
rs752884572	snp	C/G			upstream-variant-2KB	RNF157	GRCh38.p7	17:76241019	GGAAATCTCATGCAG[C/G]GGGGTAGGGAGAGGG	114804
rs752889992	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76228336	TGGTGCTCTCAGAAC[C/T]CTTATGCATTACAAT	114804
rs752906151	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76215182	GGTGTGATGGATCTT[A/G]CCTGTAATCCTAAAA	114804
rs752939507	snp	A/C	1.70177e-05	0.00291694	intron-variant	RNF157	GRCh38.p7	17:76166990	TGGATGTGGGAAACC[A/C]TCCCCAGAGGCAGCT	114804
rs753060039	snp	A/C	1.69052e-05	0.00290728	intron-variant	RNF157	GRCh38.p7	17:76155367	TAAAGGTCTCGTGAC[A/C]GCAAACCCAAACCTT	114804
rs753072473	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76206111	TGGGGCGTGCTTGTA[G/T]TCCCAGCTACTGGAG	114804
rs753081224	snp	C/G			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76144964	CCATGGACCCCAGCT[C/G]CACCTGAACATCAAT	114804
rs753110987	snp	C/T	1.73192e-05	0.00294267	intron-variant	RNF157	GRCh38.p7	17:76162052	AAAGCCCTTCCTGTC[C/T]CATACTTTACTGACA	114804
rs753120628	snp	C/G	3.33006e-05	0.00408034	intron-variant	RNF157	GRCh38.p7	17:76173839	GTTTAAAAAGACCCA[C/G]AGCTGTCCCTCGCTT	114804
rs753155571	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76238988	GCAGGTTCATCGTCT[A/G]GCCCCTGCTTTCACC	114804
rs753160582	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76218515	CCAGGCATGGTGGCA[C/T]GTGCTTGTGGTCCTA	114804
rs753164234	snp	A/G	1.64825e-05	0.00287071	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76161943	AATCAAGGTGTCCCG[A/G]ACATCCGAGAGACAC	114804
rs753165953	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76207020	GTTTAATGGTAAGAT[A/G]TAAATAAAACTTGAA	114804
rs753207306	in-del	-/GAC	1.65166e-05	0.00287368	cds-indel, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156278	TCAATAGCTCCAGAT[-/GAC]GACAAGGTGAGATTC	114804
rs753213571	snp	A/G	6.67473e-05	0.00577661	intron-variant, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156336	CCTGGGGGTTGTGGG[A/G]GGACACAACAGGACA	114804
rs753226940	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76162239	GCTCCTCCTATAAGG[C/T]CCAGAGCTGGGCCTC	114804
rs753232689	snp	C/T			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213166	TTGAAGTAGTTATTC[C/T]ATGTATTGAAGAATC	114804
rs753276973	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76184107	GAGGCAAGATAATCA[C/T]TTGAACCTGGGAGGC	114804
rs753352670	snp	A/G	3.30677e-05	0.00406605	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76159517	CGGGGTGAGGGGCCC[A/G]TTGAGGGCCTCCAGA	114804
rs753383796	in-del	-/AATC			intron-variant	RNF157	GRCh38.p7	17:76194027	AATCACATTTCTATT[-/AATC]ACCTCTTTCCAAGGC	114804
rs753395799	in-del	-/GT			intron-variant	RNF157	GRCh38.p7	17:76223920	CACCATCAGAAAGAA[-/GT]AAGTATAATAACACA	114804
rs753456294	snp	A/G	1.67055e-05	0.00289006	intron-variant	RNF157	GRCh38.p7	17:76167838	GCAGAGTAGCATATC[A/G]ATATTTTAAAATTTA	114804
rs753461773	snp	A/G			intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154194	GAGCAGCGCCACCAC[A/G]TCATACCGGTACCCT	114804
rs753483741	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76181733	GCCAACATGGTGAAA[C/T]CTCATCTCTACTAAA	114804
rs753485700	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76195713	CCGTACACAGCACAG[C/G]AATAGTTTGTTCCTT	114804
rs753486491	snp	C/G	1.66866e-05	0.00288842	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76155607	AGGCTGGGGGGAAGA[C/G]AGAGCCTCTCCCTCC	114804
rs753507516	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76223189	CCACCGCACCCGGCC[-/T]TTTTTTTTTTTTTTT	114804
rs753529840	snp	C/G	1.65701e-05	0.00287833	missense, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156306	GATTCTCACTTTCTG[C/G]AGTCACACCACATTC	114804
rs753581285	snp	A/G	1.83751e-05	0.00303104	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145357	CCTGCCAGGCACCTG[A/G]GGAAGAGAAAATGAA	114804
rs753621392	snp	A/G	4.45504e-05	0.00471945	missense, intron-variant, utr-variant-3-prime, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145276	AGGGCCTCGTCTCAG[A/G]GTCCTCCAGGCTGCT	114804
rs753628786	snp	C/T	0.000111464	0.00746456	intron-variant	RNF157	GRCh38.p7	17:76240114	CCCCTGCCCCTGCCC[C/T]TCTCCCTCCTCGCGG	114804
rs753676471	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76189405	TGAGCAGAAGGCGTG[C/G]GTCTCAGCTCCTGTG	114804
rs753679177	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76202254	TTGTGATGTGACCTA[C/T]TAGGCCAGTTACTCC	114804
rs753697079	snp	G/T	1.64901e-05	0.00287137	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159421	CCTGACGGGGGGCAG[G/T]TGGCCATCACTGCCA	114804
rs753746996	snp	C/T			intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76148509	CCTGATCTTGTGATC[C/T]GCCCATCTCGGCCTC	114804
rs753804374	snp	C/T			intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76148359	GCAAGCTCCGCCTCC[C/T]GGGTTCACGCCATTC	114804
rs753815910	snp	G/T	1.6563e-05	0.00287771	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152510	GGCTGGCTGTGTTTT[G/T]CTCTGCGTTGCTGTC	114804
rs753862416	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76188283	TCACTCCACTGCCCC[A/C]TGTGGTCACCCATCA	114804
rs753912926	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76206872	GTATAGCTAACATTG[A/C]TGCATGCTGCTTTTT	114804
rs753918747	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76238783	TTAAAAAACAAAATC[C/T]ATGCCTTGGTTAGCG	114804
rs753931614	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150098	TTGCCACAGAAGCGT[C/T]CCCATTTTTACTGAA	114804
rs753948849	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76191956	TCTTTGACAATACAA[G/T]ACAGACTTTTATATA	114804
rs753957508	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76179311	ACGCAAGAGGATCAC[C/T]TGAGCCCAGGAGATT	114804
rs753962370	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76230254	TTTCTGTCTAATTTC[C/G]CCGGATCTTGAGGCA	114804
rs753969237	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76161024	CTCTCCCAGCAGTGC[A/G]TTAGTCTAAAGAAAG	114804
rs753987010	snp	C/T	1.65452e-05	0.00287616	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76167069	GCAGAACTGCTGACA[C/T]ACTCCTCGCTTGTAC	114804
rs754011832	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76237636	GTATAGTAGGAAGAA[C/G]ACTAACTGGCTGAGA	114804
rs754128805	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151208	CTGCCTCTTTTGGTC[C/T]CACTGAAAATGAAGA	114804
rs754129387	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76178641	CCCAAAGATCACATA[A/C]TACTATGTGCCAGGC	114804
rs754133622	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76232062	AAATCATGTTGTATA[C/G]CATGTATCAGTAGTT	114804
rs754152946	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76206045	GACCAGCCTGGGCTA[C/T]GTAGTAAGACATTCT	114804
rs754183930	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76217357	TTATTGGTATTTCAT[C/T]TTACAACCAAAAATT	114804
rs754224571	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76155149	CCCTAGGAAGGCTTC[A/G]TCAGCGCAGCCTCCT	114804
rs754242632	in-del	-/TC	3.30107e-05	0.00406254	frameshift-variant, nc-transcript-variant	RNF157	GRCh38.p7	17:76158417	ATGCTGAACCGACGG[-/TC]TCTGAGAGAGCTGTG	114804
rs754248412	in-del	-/CCCCACAAAAAAAAAAAAAAA			intron-variant	RNF157	GRCh38.p7	17:76172620	TCAAAAAAAAAAAAA[-/CCCCACAAAAAAAAAAAAAAA]AAAAAAAAAAAAAGG	114804
rs754262585	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76160235	TAGTTGTGTCTAACA[C/T]ATCCTATTGTAAACA	114804
rs754286116	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76205829	AAACTGTGTCAATGC[A/G]GCCCAGCTACAGAAC	114804
rs754295832	in-del	-/G	0.000267469	0.0115613	intron-variant	RNF157	GRCh38.p7	17:76166548	GGAAAGAAAAGGAAA[-/G]GGAAAAAAAAAGAGG	114804
rs754300021	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76177170	AGGACCTGGAGCCCC[G/T]GCCCCAGGCTGCAAG	114804
rs754315440	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76216257	AGGGATCTGGGGCAG[G/T]AAAAATCCATGGATG	114804
rs754352695	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76172319	ACTCTGGGCCAGGTG[C/T]GGTGGCTCACGCCTG	114804
rs754369547	snp	C/T	3.30289e-05	0.00406366	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76158460	CTGCAGGAATGCTCA[C/T]CTTCCTCTTCATGCA	114804
rs754378026	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76218466	GGCAACATAGCAAGA[C/T]CTCATCTCTACAATA	114804
rs754466115	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76165380	GCAACCTCTTTCACC[A/C]TTATAGCCTCTAAAG	114804
rs754476415	snp	C/T	1.67239e-05	0.00289166	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76164786	TGACACAGAAAGTTC[C/T]ATCTGTGTGCTGGAA	114804
rs754530511	snp	A/G			intron-variant, upstream-variant-2KB, downstream-variant-500B	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142251	TGGGTTGATTACCCC[A/G]CCTCTGCCCAGGAGC	114804
rs754558822	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76230555	TCTTAAAAGGAGATA[C/T]TGAGCCGGGCATGGT	114804
rs754561871	snp	A/G	1.65957e-05	0.00288055	intron-variant	RNF157	GRCh38.p7	17:76159304	TCATCAAGGATTCCG[A/G]GGGCAACAGTGTGGA	114804
rs754568038	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76209702	ATGAAAGGAAAAAGA[C/T]AGAAACAGATGCAAA	114804
rs754569830	snp	C/T			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76214032	AGTTCTGTGAGTCCC[C/T]CTAGCAAGTTAATCA	114804
rs754599945	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76197945	CCCTAGGCTTGCAAA[C/T]AGCCCTCTCCCTTGA	114804
rs754629310	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76216548	GCCCAGGAGCTCAAG[-/A]CCAGCCTAGGCAACA	114804
rs754680265	in-del	-/CTTT			intron-variant	RNF157	GRCh38.p7	17:76190170	AACTGCTTGCTCTCT[-/CTTT]TTTTTTTTTTTTTGA	114804
rs754682297	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76181798	CTGTACTCCCAGTTA[C/T]TCAGAAGGCTGAGGC	114804
rs754686932	snp	C/T	1.64781e-05	0.00287033	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154357	AAGGCCCTGTGAGTC[C/T]ATGAAGCGGCAAAAT	114804
rs754712037	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76221948	TAGTATGATTCCATG[C/T]ATATGAAATATCCAG	114804
rs754719411	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76229413	GAGACAATAATACTT[C/T]TTTCAACAGATTATT	114804
rs754721484	snp	G/T	4.96397e-05	0.0049817	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167115	TGGAGGCTGTTGTCT[G/T]TGGGAATGTAGCTAT	114804
rs754723617	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76190738	CGATGAAACCCCGTC[G/T]CTACTAAAAACACAA	114804
rs754801899	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76234394	TTGAGCGTATACCTA[A/G]GAGTAGAACTGCTGA	114804
rs754802777	snp	C/G	3.46063e-05	0.00415956	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76155646	GCCAGGGGCGATGTA[C/G]GAGCCAGACATGGAG	114804
rs754841953	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76187578	ATAGCATATACCTGA[C/T]AGTTTTATTTTATTT	114804
rs754858020	snp	C/T	4.23236e-05	0.0046	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155729	CCAAGCTGCTGCTGG[C/T]AGGGCCTTTGGAGAC	114804
rs754867109	snp	G/T	4.58526e-05	0.00478792	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76173766	TCTTCACGGGTTCTT[G/T]GGGAGGTGGGGCGGC	114804
rs754869484	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76208490	CAAAATGAGACAACA[C/T]AGATGAAAAGCTTAG	114804
rs754886219	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76176461	TTGTCTCCCATTCTT[C/G]TGTAAATCGATTTTG	114804
rs754979955	in-del	-/C	3.74834e-05	0.004329	intron-variant	RNF157	GRCh38.p7	17:76173681	GTGCCTGGGACCTGG[-/C]CCCAGCCTCTGGGAA	114804
rs755001054	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76193110	AGGCGTGGGCCAGAG[A/C]ACTCAGCCTTCTCTC	114804
rs755006202	snp	C/G			intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76148678	CAGGCTCAATTGATC[C/G]TCCTGCCTCAGCCTC	114804
rs755037732	snp	A/G	3.33495e-05	0.00408333	intron-variant, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156334	TTCCTGGGGGTTGTG[A/G]GGGGACACAACAGGA	114804
rs755059741	snp	C/T	5.96534e-05	0.00546106	intron-variant	RNF157	GRCh38.p7	17:76240147	GCGGCGCCCGCCCGC[C/T]CTCACCGGACTTGGG	114804
rs755119995	snp	A/C	4.82707e-05	0.00491254	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76240234	GCCGGCTCGTCAGGG[A/C]CCCCATGGCCGCTGC	114804
rs755137164	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76238831	TAATCAGTCAGAGCT[G/T]TATTAAAATACTAAC	114804
rs755171260	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76182248	TGGTGGACCTCAGGC[A/G]TTTGCTGACGAAGGC	114804
rs755214755	snp	G/T	1.64931e-05	0.00287163	intron-variant	RNF157	GRCh38.p7	17:76165577	CACGTGAGTGAAGAA[G/T]CCCAAACAGCACATC	114804
rs755219227	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76224260	GACATATTCCTAATA[A/C]CACAGTGAAATTAAA	114804
rs755227603	snp	A/T			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212607	TGGCTCACACCTGTA[A/T]TCCCAGCACTTTGGG	114804
rs755234792	snp	A/C/G	0.000131996	0.00812304	intron-variant, missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155256	GTTGGGGTTACCTCT[A/C/G]CATCCTGCTCTCCAG	114804
rs755241895	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76179408	AAAAGGAAAAAAAAA[G/T]AGGCCAAGCGTGGTG	114804
rs755261505	snp	A/T	1.64917e-05	0.00287151	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76166487	TCCACCACGGCATGT[A/T]CCACTAGAGGGTAAA	114804
rs755263225	snp	C/G	1.654e-05	0.00287571	intron-variant	RNF157	GRCh38.p7	17:76167605	CTCTTCCGTGGCCTG[C/G]TAATAATCTGGGAAG	114804
rs755363772	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76172348	TGTAATCCCAGCACT[C/T]TGGGAGGCTGAGACG	114804
rs755366496	snp	C/G			utr-variant-3-prime, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76143328	TCTCCTTCATCTCAG[C/G]TCCTTCCTCCCTCCT	114804
rs755370751	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76236424	ATCTCCGCAAAGCCA[A/T]ACCTTTCTTTGCTAA	114804
rs755377700	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76161128	AAGTCAGTTACTTTA[C/T]CTCAGGCACTGAGGC	114804
rs755414599	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76209638	ATCATCTTTATGGAC[C/T]GAAAAGGCCAAAATT	114804
rs755416493	in-del	-/AC			intron-variant	RNF157	GRCh38.p7	17:76163423	GGTCTCAAACTCCTG[-/AC]ACCTCAAGTGATCCA	114804
rs755448266	snp	C/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150263	GAGAGCCAACACAGG[C/G]ATTTGATTTCGTGTC	114804
rs755466972	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76205911	CTTATAAAATGAGAG[A/G]AGCGGTTTGAACTCC	114804
rs755479213	snp	C/T	6.60589e-05	0.00574675	missense, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156251	AGAGGCGTCCCTGTG[C/T]AAGACGACTGGTCAA	114804
rs755499102	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76190313	CTAGGTCCACAGGCA[C/T]GTGCCACCATACCCA	114804
rs755510415	snp	C/T	3.29641e-05	0.00405968	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161941	AGAATCAAGGTGTCC[C/T]GGACATCCGAGAGAC	114804
rs755520382	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76237686	CATTTCTCTGGGTCT[C/T]CATTTTCTTATCAGT	114804
rs755573593	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76210434	CTCTACTAAAAATAC[-/A]AAAAAATTAGCCGGG	114804
rs755589202	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76176298	TCATTTCTGGCTGAG[A/G]TAATCTGAAGGCTTC	114804
rs755646129	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76211008	TAGGGTTTCACCATG[-/T]TGGCCAGGCTGGTCT	114804
rs755659505	snp	C/T			intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153463	TGACATCTGCTGGTG[C/T]GTCTGTATCCAGGCC	114804
rs755672979	snp	C/T	1.64991e-05	0.00287215	intron-variant, missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155268	TCTGCATCCTGCTCT[C/T]CAGCTGGGAGGCCAG	114804
rs755679066	snp	A/C			intron-variant, splice-donor-variant	RNF157	GRCh38.p7	17:76175747	TATCCATAACTCCTA[A/C]CTGCATTTCAAAAAA	114804
rs755703373	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76190841	CGAACCCGGGAGGCG[C/G]AGCTTGCAGTGAGCC	114804
rs755765020	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76219639	ACATAATTATAAAAT[C/T]AAAATTTCTGTAAAG	114804
rs755786773	snp	C/T	3.30267e-05	0.00406353	intron-variant	RNF157	GRCh38.p7	17:76167628	CTGGGAAGGAAGTGG[C/T]TCTCCTGGTCTCCTG	114804
rs755787562	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76163833	GCCTGGCCTGCCCAG[A/G]TAGTGCCCTGGGCCT	114804
rs755815524	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76209570	ATTCTTCTTCTTCCA[A/G]TGTGGCCCAGGGAAC	114804
rs755840128	snp	C/T	1.64746e-05	0.00287002	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167744	AACTCAACATTGTAG[C/T]GGACTTTAGCTTTAC	114804
rs755850316	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76165048	TCTTAGTCTCTTACT[A/G]TGCCTAACTTATGAA	114804
rs755907056	snp	A/G	3.29473e-05	0.00405864	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF157	GRCh38.p7	17:76212393	TCCCCAGAAAGTTCA[A/G]ATCGCTGTTCTCTCC	114804
rs755927532	snp	A/G	8.26385e-05	0.00642747	synonymous-codon, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156226	TTCTGGGGAGGAAAT[A/G]GTGGATGACAGAGGC	114804
rs755986929	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76199508	ATCCTCCCACTTTGG[C/T]CTCCCAAAGTGCTGG	114804
rs756016297	snp	C/T	0.000159096	0.00891756	synonymous-codon, intron-variant, utr-variant-3-prime, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145268	CCACACACAGGGCCT[C/T]GTCTCAGAGTCCTCC	114804
rs756027019	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76202639	ATTAGAGCGCTACTA[-/T]TTTTTTTTTTCAGGC	114804
rs756027844	snp	A/G	1.68457e-05	0.00290216	intron-variant	RNF157	GRCh38.p7	17:76164798	TTCCATCTGTGTGCT[A/G]GAATGAAAATATGAA	114804
rs756035996	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76178561	GGTGGAAGAAGCCCA[A/G]TGTGCCTGAGCCGAA	114804
rs756046199	in-del	-/T			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76148261	CAAATTATCTTTGCC[-/T]TTTTTTTTTTTTTTT	114804
rs756047532	snp	A/G	1.65941e-05	0.00288041	intron-variant	RNF157	GRCh38.p7	17:76159307	TCAAGGATTCCGGGG[A/G]CAACAGTGTGGAGCA	114804
rs756048273	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76234282	TTATCAGTAGTTCTA[C/T]TCATCGGTTGATGAA	114804
rs756065012	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76233465	ACTCTTCGCCCAATC[A/C]AAATCAAATAACATT	114804
rs756090794	snp	C/T			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76148011	ATATAAGGACTGTAA[C/T]AGTTCAACTGTCTTT	114804
rs756161988	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76160056	AGCTCCTGGTCTCAA[C/T]TGATCCTCCCACCAT	114804
rs756249791	snp	A/C/G			intron-variant	RNF157	GRCh38.p7	17:76158892	CCACTGCCATTTACA[A/C/G]GGTCTCAATATTTTC	114804
rs756350798	snp	A/G	1.65952e-05	0.00288051	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159555	CTACTTCATAGCCTG[A/G]TGGAATATTCTCTGA	114804
rs756353212	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76225246	ATCCCAGCACTTTGG[A/G]AGGCTGAGGTGGGAG	114804
rs756356230	snp	A/C			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149924	CTGTAATCCCAGCTA[A/C]TCAGGAGGCTGAGGC	114804
rs756357799	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76202616	GCAAAGCTTCCTTAA[C/T]TGTGAGCTATTAGAG	114804
rs756407645	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76177365	CCTAGCTTCTGCTTG[A/C]TCTTGGTGCTGGCTC	114804
rs756439364	in-del	-/A	1.66877e-05	0.00288852	intron-variant, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156336	CTGGGGGTTGTGGGG[-/A]GGACACAACAGGACA	114804
rs756482248	snp	A/G	1.67304e-05	0.00289222	intron-variant, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156339	GGGGGTTGTGGGGGG[A/G]CACAACAGGACATGG	114804
rs756482270	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76180845	TCGTGCGGCCATCAC[C/T]GCCATCCAGCTCTAG	114804
rs756503220	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76229364	CCAGGACAAATTATT[G/T]AAACTTTTTGAGCTT	114804
rs756580909	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76184471	TATTTTTAGACTGGT[A/G]ATGGATCAGTGTTGG	114804
rs756591481	in-del	-/AG			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213552	TCCAGCCTAGGTGAC[-/AG]AGCAAAACTCCATCT	114804
rs756593912	snp	C/T	1.854e-05	0.00304461	intron-variant	RNF157	GRCh38.p7	17:76162505	GCTTACGATTTCTCA[C/T]TTGGCCTCCTGGAAA	114804
rs756609733	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76217316	GCCCAGCCATCCTCA[A/T]CTGTTAAAAGGAAAA	114804
rs756643684	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76202633	GTGAGCTATTAGAGC[A/G]CTACTATTTTTTTTT	114804
rs756658157	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76171345	AGATGCGTGCCACCA[C/T]GTCTGGCTAATTTTT	114804
rs756672678	snp	C/T	1.65089e-05	0.00287301	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76158403	ATTACCTCTCCGAGA[C/T]GCTGAACCGACGGTC	114804
rs756678125	in-del	-/GTAA			intron-variant	RNF157	GRCh38.p7	17:76193397	AATACAAGCAATTAG[-/GTAA]GTATCTCTTATCTAC	114804
rs756700659	snp	C/T	1.64762e-05	0.00287016	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76167764	TTTAGCTTTACTGGC[C/T]TCTTCTCCAGGGCTC	114804
rs756705130	snp	G/T	0.000104477	0.00722686	utr-variant-5-prime, nc-transcript-variant	RNF157	GRCh38.p7	17:76240253	CATGGCCGCTGCGGC[G/T]GCAGCCCCGGCCCGG	114804
rs756741685	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76195891	TACCTCCCATACCTG[C/T]CAGTGTGTGCCATGT	114804
rs756746320	snp	C/G	1.68912e-05	0.00290608	intron-variant	RNF157	GRCh38.p7	17:76155528	TGTGCACAAAGAACA[C/G]AGAAGCCAGGGCGGT	114804
rs756748708	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76173990	AAACTGGGATGCAAT[C/T]TGGGGCCCAAAGAGC	114804
rs756759219	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76219854	GACAGTATTTTCTTC[C/T]GAGAATGTGGCATTA	114804
rs756847805	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76236873	AACAGAGCAAGGTGT[A/G]GAACAGTCTAATAGC	114804
rs756849520	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76218683	TCACACCTGTAATCC[C/G]AGCACTTTGGGAGGC	114804
rs756870329	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76175418	AAAAATTATTTTGCC[A/G]AACAGTTTTCCACAA	114804
rs756895757	snp	A/G	1.67058e-05	0.00289009	intron-variant	RNF157	GRCh38.p7	17:76167839	CAGAGTAGCATATCA[A/G]TATTTTAAAATTTAC	114804
rs756932914	snp	C/T	1.66615e-05	0.00288626	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161990	TGTTATCACTCACTT[C/T]GTCTTCAGCCACCTG	114804
rs756937893	snp	C/G	0.000148259	0.00860858	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF157	GRCh38.p7	17:76212379	CACAACTGGTCTGTT[C/G]CCCAGAAAGTTCAGA	114804
rs756984198	snp	C/T	1.84483e-05	0.00303707	intron-variant	RNF157	GRCh38.p7	17:76162511	GATTTCTCACTTGGC[C/T]TCCTGGAAAGAGTAC	114804
rs757018435	snp	A/G	1.83967e-05	0.00303282	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145363	AGGCACCTGGGGAAG[A/G]GAAAATGAACATTAC	114804
rs757019555	snp	C/T			intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76148556	ACAGGCGGGAGCCAC[C/T]GTGCCCCGCCTTTTT	114804
rs757028557	in-del	-/TTTCTA			intron-variant	RNF157	GRCh38.p7	17:76224386	GACAATTAAACCCAT[-/TTTCTA]TTTCTATTCTTCTAC	114804
rs757072801	snp	C/G			utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76143654	TGTGAGCCACAACCA[C/G]TAGGCAGTGAGACAG	114804
rs757092710	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76180461	ACCTGCAATTACAGC[C/T]TGGCAAATCATGAAA	114804
rs757109570	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76232422	AAACAAACAAAAAAT[C/T]AAATTGCTGAGCAGT	114804
rs757149605	snp	C/T			intron-variant, downstream-variant-500B	RNF157	GRCh38.p7	17:76155862	GTATCTTGCCCTCCC[C/T]TAAAAGTGGTTTTAG	114804
rs757150273	snp	C/T	1.65474e-05	0.00287636	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76159526	GGGCCCGTTGAGGGC[C/T]TCCAGAAGAGATACT	114804
rs757170132	snp	C/T	1.64904e-05	0.00287139	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159422	CTGACGGGGGGCAGG[C/T]GGCCATCACTGCCAT	114804
rs757171978	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76165837	ATGAGCCACCATGCC[C/T]GGTTACTTTTCTGTA	114804
rs757173983	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76178554	CCAAGTGGGTGGAAG[A/G]AGCCCAATGTGCCTG	114804
rs757191759	snp	G/T	1.65075e-05	0.00287289	intron-variant, missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155288	TGGGAGGCCAGCAAA[G/T]TTGCTGTCTGGAGAC	114804
rs757230373	in-del	-/CAAC			utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144685	AAGGATTGTTTCCTT[-/CAAC]CAACCTTTTGGTTGC	114804
rs757293950	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76157747	ACTTTATTTACCTTC[C/T]TGTGCCCTGCTGTAT	114804
rs757296112	snp	C/T	1.65425e-05	0.00287593	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167074	ACTGCTGACACACTC[C/T]TCGCTTGTACTGCAC	114804
rs757331475	snp	A/G	6.59239e-05	0.00574087	intron-variant	RNF157	GRCh38.p7	17:76161522	AGGGGCCGTGGTTCC[A/G]AGCCCAACTTACTGG	114804
rs757374111	snp	A/C	1.64849e-05	0.00287092	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161616	GCCCAATTTTTTCCT[A/C]ATGGCTCGGATCTGA	114804
rs757383042	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76170003	TTAAACTGCTGATTA[G/T]AGCTCTGAGTGCACA	114804
rs757445002	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76203039	CGTCCAGCCCAGGCT[A/G]GAGTGCAGTGGCATG	114804
rs757466773	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76235497	GCCACTGCGCCCAGC[C/T]GTAAATTGCATATTT	114804
rs757491791	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76158877	TAAACTTGGGAAAAA[A/C]CACTGCCATTTACAG	114804
rs757511562	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76203061	AGTGGCATGATCTCC[A/G]CTCGCTGCAACCTCC	114804
rs757581496	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76227544	AGAAGAGGAAACTAA[C/T]GCACAGAGGTTAAAT	114804
rs757605968	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76194767	ACACCTGTAATCCCA[C/G]CACTTTGGGAGGCCA	114804
rs757621322	in-del	-/TTTGAG	1.65149e-05	0.00287353	cds-indel, nc-transcript-variant	RNF157	GRCh38.p7	17:76159349	CTTGGAGAGACTCTT[-/TTTGAG]TTTGAGTCCCTGACT	114804
rs757641388	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76187633	GGTTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC	114804
rs757727032	in-del	-/CGAAC			intron-variant	RNF157	GRCh38.p7	17:76226524	ACAGGGCACCAAAGT[-/CGAAC]TCCTTCAAATCCATT	114804
rs757745909	snp	C/T	1.65157e-05	0.0028736	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76158461	TGCAGGAATGCTCAT[C/T]TTCCTCTTCATGCAG	114804
rs757748060	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76208340	AATTAGCAAAAATGG[C/T]AGCATGGTTCAGGCT	114804
rs757755714	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76228877	TGCAGTGAGCTGAGA[C/T]TGCGCCATTGGACTC	114804
rs757773775	snp	A/G			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76214001	CTTGATAATAAACTC[A/G]TAAATGTGTTTCTCT	114804
rs757783677	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76180748	TTTATCTTGGTAAAA[G/T]ACACATAACATGAAA	114804
rs757814827	snp	C/T	4.97327e-05	0.00498637	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152513	TGGCTGTGTTTTTCT[C/T]TGCGTTGCTGTCCTT	114804
rs757888151	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76183660	CATTAAAAAACATTT[A/G]TGGATATAGAATAAT	114804
rs757979686	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76218571	GATTGCTGGAGGTCA[A/G]GGCAGGAGTGAGCTA	114804
rs757990330	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76166860	TGCAAAATAAGCAGA[C/G]CTTTAAAAGGACATG	114804
rs758004042	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76185144	TGAGACTGGGCAACA[G/T]GCTCAGTCCCACTCT	114804
rs758023050	snp	G/T	1.6755e-05	0.00289435	intron-variant	RNF157	GRCh38.p7	17:76162642	AACAGCAAACAGAAA[G/T]GTTCAAGGACAGGCT	114804
rs758076307	snp	C/T	1.65211e-05	0.00287407	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76158472	TCATCTTCCTCTTCA[C/T]GCAGCACGGAAGAGT	114804
rs758076883	snp	A/G			utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76143578	GGCCTGAAATGGTAA[A/G]GTCTACTGCAGTTTT	114804
rs758121881	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76209884	CCTGCCTCAGCCTCC[G/T]GAGTAGCTGGGACTA	114804
rs758142401	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76172539	GAGGTTGCAGTGAGC[C/T]GAGATCGCAGTGAGC	114804
rs758207638	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76223524	ATACCTGACTCTTCC[G/T]TTTCCTGTACTGTAA	114804
rs758260386	snp	A/G	3.37245e-05	0.00410623	intron-variant	RNF157	GRCh38.p7	17:76155541	CAGAGAAGCCAGGGC[A/G]GTTCCCGTCCCTTCC	114804
rs758261075	snp	C/T	1.65685e-05	0.00287819	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76159538	GGCCTCCAGAAGAGA[C/T]ACTACTTCATAGCCT	114804
rs758266773	snp	A/G			intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154617	ATACTGTTTCTCTAA[A/G]GTGGAAGTAAAAATT	114804
rs758276353	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76176611	GGCTGCTGCAGGGGG[G/T]TCGCAGGGAGCAGAC	114804
rs758330715	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76189695	CGGTTTCCATCCCCA[C/T]GGCTGAGGAAACAAA	114804
rs758387667	in-del	-/AAC			intron-variant	RNF157	GRCh38.p7	17:76192522	TAGAATGAATACACG[-/AAC]AACAAGATCTTCGGA	114804
rs758391889	snp	A/G	1.65277e-05	0.00287464	intron-variant	RNF157	GRCh38.p7	17:76173668	TCCCCAAAGGAAGGT[A/G]CCTGGGACCTGGCCC	114804
rs758415701	in-del	-/A	1.65762e-05	0.00287886	intron-variant	RNF157	GRCh38.p7	17:76167161	CAAAGCAAAAGTCAG[-/A]TATCCGGCACAGATG	114804
rs758445078	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76180509	ATATTTAACTGAGTA[G/T]CTACTATGTGCCAGG	114804
rs758458767	in-del	-/A	1.64953e-05	0.00287182	frameshift-variant, nc-transcript-variant	RNF157	GRCh38.p7	17:76159483	TCCAAGCACGTGAAG[-/A]TGGAGGAACTGCTGG	114804
rs758471629	snp	C/T	1.67657e-05	0.00289527	intron-variant	RNF157	GRCh38.p7	17:76161802	AATGTCCTCTTGTCC[C/T]CTCTCCCACCCACCA	114804
rs758482572	snp	A/C			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213905	CTGGAGGGTAACATG[A/C]CCAGAGACGGCATAG	114804
rs758492532	in-del	-/T/TTTTTTTTTTTTTT			intron-variant	RNF157	GRCh38.p7	17:76185475	GAGATTAGTCCTTTC[-/T/TTTTTTTTTTTTTT]TTTTTTTTTTTTGAG	114804
rs758500056	snp	A/G	1.7879e-05	0.00298985	intron-variant	RNF157	GRCh38.p7	17:76155779	CTGGAGGTCAGGCAG[A/G]GCTTCTGCAAGCTTT	114804
rs758533085	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76179496	CAGGAGCTTTGAGAC[C/T]GGCCTGGCCAACATA	114804
rs758572194	snp	C/T			intron-variant, nc-transcript-variant	RNF157	GRCh38.p7	17:76156460	GTGGCATGCAGAGGC[C/T]GCAGCTTCTCTCTTC	114804
rs758580108	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76157584	GACACAGCAATTTAT[C/T]GTCTCTGTTTTGGGC	114804
rs758580631	snp	G/T	2.18167e-05	0.00330271	missense, intron-variant, utr-variant-3-prime, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145286	CTCAGAGTCCTCCAG[G/T]CTGCTGGATGACAAG	114804
rs758608990	snp	A/G	3.43218e-05	0.00414243	intron-variant	RNF157	GRCh38.p7	17:76164823	TATGAAAGTTATGAC[A/G]AGGAAGGGAGGGTAA	114804
rs758626398	snp	A/G	1.64784e-05	0.00287035	missense, utr-variant-5-prime, nc-transcript-variant	RNF157	GRCh38.p7	17:76212429	GGTAACCTTCAGGAT[A/G]AGTTGAGTCAAACTT	114804
rs758695882	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76210892	TCACTGCAACCTCCA[A/C]TTCCCGGGTTCAAGC	114804
rs758720285	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76192165	TTTCGAGGAAATTCC[C/T]ACAACACAGATGCTT	114804
rs758745841	in-del	-/C			intron-variant	RNF157	GRCh38.p7	17:76225837	TGGCCAGGGAATCTG[-/C]CCTCTCTTTTAGAGC	114804
rs758749102	in-del	-/AGA			intron-variant	RNF157	GRCh38.p7	17:76164676	AAAAAAGAGGGAGAG[-/AGA]AGAAGAAAGGAAAGA	114804
rs758749297	snp	C/G	1.7013e-05	0.00291654	intron-variant	RNF157	GRCh38.p7	17:76240130	TCTCCCTCCTCGCGG[C/G]TGCGGCGCCCGCCCG	114804
rs758749632	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76207064	CTTTCTTCCACCATC[C/T]TTCTGTATATACACA	114804
rs758764448	snp	A/C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151993	TCCTTCCAAGACCTT[A/C/T]GTAGAGAGGTGGTGT	114804
rs758790988	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76164210	GAAAAGTGCTGGCAC[A/G]TGGTAGGGGCTGGGA	114804
rs758801046	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76160782	TCTTGCTTTCAAGCT[G/T]AGAGAATCCTTTCCA	114804
rs758805162	snp	A/C			upstream-variant-2KB	RNF157	GRCh38.p7	17:76241179	TGTAGCCCTAAAGTT[A/C]GGAGAACATCGACTG	114804
rs758814837	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76161257	CCTGGGGGAGTTCAA[A/G]TTGAACCTCACTGGA	114804
rs758824574	snp	C/T	1.64798e-05	0.00287047	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154234	CCCTTAAAGAATACC[C/T]AGGAAAGAAAGATAA	114804
rs758840285	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76217598	TAGACAGCTTATGCA[-/T]ATTTTTACTTCTTAA	114804
rs758918306	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76193467	ATATCTCACTTGGTC[A/G]TGACCCAGAAGAATT	114804
rs758961802	snp	A/G	3.31713e-05	0.00407242	intron-variant	RNF157	GRCh38.p7	17:76167167	CAAAAGTCAGTATCC[A/G]GCACAGATGGGTCTG	114804
rs758966652	in-del	-/TAAA			intron-variant	RNF157	GRCh38.p7	17:76205727	GACTCCATCTCTAAA[-/TAAA]TAAATAAATAAATAA	114804
rs758976149	snp	A/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151346	GCTTGTGTGGGGCCA[A/G]AGTGTGCTTGGACTG	114804
rs758993578	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76162249	TAAGGCCCAGAGCTG[A/G]GCCTCTCAAATCTCA	114804
rs758998472	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76239055	ATCTCAGTATGTCTC[C/T]ATTCTACCAAAAAGA	114804
rs759017594	snp	A/G	1.66618e-05	0.00288628	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76240179	GGGTAGCGGTACACG[A/G]AATTAGACGGGATGT	114804
rs759044828	snp	G/T	5.06e-05	0.00502966	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212491	TAGCTTCCTAGAGAG[G/T]AACAAACAAAAAAAA	114804
rs759092284	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76238350	ATGTGGTCCACTTGC[C/T]ATAAAGACTTCTCTC	114804
rs759093951	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76224836	GCCCAGCCCATGGGG[C/T]GTGGGTTGTACAAAC	114804
rs759094082	snp	C/G	1.64898e-05	0.00287135	intron-variant	RNF157	GRCh38.p7	17:76165484	GGCAATAAAGCGAGG[C/G]CCTCTAAAGTCACTC	114804
rs759138991	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76179649	AGTGAGCTGAGCTCA[G/T]GCCACTGCACTCCAG	114804
rs759176175	snp	C/T			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147674	ACCCTGAGGGGCCCA[C/T]GGCAAAGCCCTGCTG	114804
rs759187382	snp	C/T	5.61183e-05	0.00529679	missense, intron-variant, utr-variant-3-prime, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145327	GGGCATTCCGACTGA[C/T]GGCATTGTCATCAGC	114804
rs759216847	snp	A/C	1.64871e-05	0.00287111	intron-variant	RNF157	GRCh38.p7	17:76166437	GCAGTGTGCACAGCC[A/C]AAGAGGACAGAAATC	114804
rs759240120	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76211856	TGTATTCTCATATCA[A/G]CTCATATATCAAGAG	114804
rs759268660	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76179010	TTATTTTCTCATTCC[C/T]TTCTAAAGTCAAGAC	114804
rs759300142	snp	G/T	5.03808e-05	0.00501875	intron-variant	RNF157	GRCh38.p7	17:76161698	ATACAGGATTAAGAA[G/T]GAACAAGAGCCCAGA	114804
rs759302401	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76171782	CAAGCAAGCATCTGT[A/G]GACCTGGGAGGCAAA	114804
rs759345123	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76162221	ACGAGACTAACCACT[C/T]GAGCTCCTCCTATAA	114804
rs759388679	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76182353	ACATCGGCAAAGCGC[C/T]ACCTGGTGACGAAAG	114804
rs759489012	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149866	TGGTAAAACTCCGTC[C/T]CTGCTAAAAATACAA	114804
rs759546466	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76205089	ACCATGCCCAGTCTC[C/T]TTCCTTCCTCCCTCC	114804
rs759562324	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76208079	CACCACCACGCCTGG[C/T]TAATTTTTATCATTT	114804
rs759581027	snp	A/C	1.65312e-05	0.00287495	missense, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156223	ACCTTCTGGGGAGGA[A/C]ATAGTGGATGACAGA	114804
rs759585000	in-del	-/A			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151091	CTCCAGTCCAGGCCT[-/A]ACTGGCAGGAGGCTG	114804
rs759648061	snp	C/T	1.65149e-05	0.00287353	intron-variant	RNF157	GRCh38.p7	17:76158389	GGAGAGGAATGTCAA[C/T]TACCTCTCCGAGATG	114804
rs759649018	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76162151	GTCATTTTCCCAGTG[C/T]GTCCACACACTTAGC	114804
rs759669945	snp	C/T			upstream-variant-2KB	RNF157	GRCh38.p7	17:76242233	AGAATCTAGAACCAC[C/T]TCAAAACACAAGGCC	114804
rs759698353	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76220881	GAGAATCACTTGAAC[C/T]GGGGAGGCAGAGGTT	114804
rs759700011	snp	C/T	1.66153e-05	0.00288225	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76162589	TTGTTTTCAATTCCA[C/T]AGATCTCCTGAAGGA	114804
rs759720926	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76163003	AGTTCAGACATTATA[C/T]AAATAAAGGAATGGA	114804
rs759772932	snp	A/G	1.64819e-05	0.00287066	synonymous-codon, intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152407	TGCTTTCACGCTTGC[A/G]ATGTCAAAGTCATTG	114804
rs759794085	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76200314	CCAATAGCCAAAAGG[C/T]AGGAGCAACCCAAGT	114804
rs759836875	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76227025	GTGGACCCTGAGGGC[A/G]GGGAGGAGGGAAGGC	114804
rs759844709	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151824	GGGATCCAAATCCAG[C/T]AGTATGTACAATGCA	114804
rs759943986	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76219506	AAATCATAATAATCT[G/T]AAAGTGATTATCTAT	114804
rs759964177	snp	C/T	1.65622e-05	0.00287764	intron-variant	RNF157	GRCh38.p7	17:76167821	CCAGAGACTCAGCAT[C/T]TGCAGAGTAGCATAT	114804
rs759986748	snp	C/T	1.68021e-05	0.0028984	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155582	CTTCTTCTGAGGGGG[C/T]CCTGCTGGCAGGCTG	114804
rs760001054	snp	C/T			utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76144893	AACAAAGCTGCCAAA[C/T]TCTAAGCCTTCTTGT	114804
rs760010514	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76198800	AATTCGAAGCTCACA[C/G]GGAGGCATACCAGGC	114804
rs760036800	snp	C/T	1.64735e-05	0.00286993	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167738	AAGGTGAACTCAACA[C/T]TGTAGTGGACTTTAG	114804
rs760038942	snp	C/T			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145784	ACTGTTCGTTCTGGC[C/T]GAGTGTTAATGTTTT	114804
rs760080849	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76189244	AATGTGTTGCAGTTA[C/T]GTAAGATGTTAACCT	114804
rs760153636	in-del	-/TTC			intron-variant	RNF157	GRCh38.p7	17:76169181	CTATTACTTGCGTCT[-/TTC]TTCTTCTATTTTCCT	114804
rs760154306	snp	A/G	5.38044e-05	0.00518645	intron-variant	RNF157	GRCh38.p7	17:76166551	AAAGAAAAGGAAAGG[A/G]AAAAAAAAGAGGACT	114804
rs760229304	snp	A/G	8.24273e-05	0.00641926	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76166462	GAAATCGCCCCTACC[A/G]TCTCCTTCATCCACC	114804
rs760255118	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76165119	CACAGTGTATATGAG[A/G]GTTCTGTACGATCTG	114804
rs760343025	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76176907	CTGTGCCCACCCTGC[C/T]GAGGGTGCCAGGTTC	114804
rs760377371	snp	A/G	1.64871e-05	0.00287111	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161876	AGTTGTTGGCCTGGT[A/G]GCGCAGCGTGTCTGC	114804
rs760428369	snp	A/G	1.65449e-05	0.00287614	synonymous-codon, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156289	AGATGACGACAAGGT[A/G]AGATTCTCACTTTCT	114804
rs760454160	snp	G/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149802	ACTTTGGGGGGCCGA[G/T]GTGGGCAGATCACCT	114804
rs760489615	snp	A/C	9.90712e-05	0.00703746	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212534	AAAACAGTCAACCTA[A/C]ATCTAGTAAAAAAAA	114804
rs760520630	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76195828	GACTAAATTGAGCAC[A/G]AGCTAAAACAGGGAC	114804
rs760531552	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76205854	CAGAACACACGAGAG[C/G]ATACAGACTATTAGG	114804
rs760589636	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76179836	TCAGGGCCAAGCATT[C/T]TTCTGAAGTACTCAT	114804
rs760599587	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76228261	AGGCACACATCAATG[C/T]GTCTAAAACCCTTCC	114804
rs760632309	snp	A/C/G	8.25381e-05	0.00642363	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76158412	CCGAGATGCTGAACC[A/C/G]ACGGTCTCTGAGAGA	114804
rs760661222	snp	C/G/T	3.30203e-05	0.00406316	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76158448	GTCTCCGACTCGCTG[C/G/T]AGGAATGCTCATCTT	114804
rs760669196	in-del	-/C			intron-variant	RNF157	GRCh38.p7	17:76223041	GACTACAGGCGCCCG[-/C]CACCATGCCTGGCTA	114804
rs760674527	snp	A/G	6.52124e-05	0.00570981	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76240193	GGAATTAGACGGGAT[A/G]TCCACCTCCTCCACG	114804
rs760685040	snp	A/G	1.65233e-05	0.00287426	intron-variant	RNF157	GRCh38.p7	17:76158376	ACACCCAAGAAGAGG[A/G]GAGGAATGTCAATTA	114804
rs760710725	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76219349	TATAACATAAAATGG[C/T]CAGCCTTAAGCCAAA	114804
rs760713433	snp	G/T	4.96364e-05	0.00498154	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152498	CAGTTAGAGAGGGGC[G/T]GGCTGTGTTTTTCTC	114804
rs760757940	in-del	-/CT			intron-variant	RNF157	GRCh38.p7	17:76190164	CAGGCTAACTGCTTG[-/CT]CTCTCTTTTTTTTTT	114804
rs760762867	in-del	-/AG			intron-variant	RNF157	GRCh38.p7	17:76231000	TAGAGTGCAGTGACC[-/AG]AGATCATAGTCCACT	114804
rs760771855	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76205705	ACTCTAGCCTGGCGA[C/T]GGAGCAAGACTCCAT	114804
rs760788035	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76173547	GGCCTGATCTCAGCA[A/G]AAAGTAGCGCCCGCA	114804
rs760792890	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76218380	GCCCAGTGGCTCACG[C/T]CTGCAATCCCAGTAC	114804
rs760796687	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76233117	AGCAGAGACAGGGTT[G/T]CACCATGTTAGCCAG	114804
rs760814766	snp	A/G			utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144647	CATGTGAGGCCCAGA[A/G]GACTGGCTCTGCCAC	114804
rs760821805	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76206734	CGGCTCACTGCAATC[A/G]GCTCACTCCAGCCTG	114804
rs760824432	snp	C/T	1.66574e-05	0.0028859	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76164748	TCTTCAAATACTTAC[C/T]ACTTGTTTCTGTTTG	114804
rs760840303	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76174523	TCTGAGGATCAAGAA[C/T]GATTTCAAATGTTCC	114804
rs760847828	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76191907	AGGGACAAAATTTAC[A/G]TGTAATCAACTGTTA	114804
rs760864185	in-del	-/CTCTCT			intron-variant	RNF157	GRCh38.p7	17:76190164	CAGGCTAACTGCTTG[-/CTCTCT]CTTTTTTTTTTTTTT	114804
rs760904217	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76184843	AAAGCACTCCATTTA[C/T]AGTCTTCGAACTCCT	114804
rs760948820	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76238746	AGTTTTCCTCATGCC[A/G]CCCTAAGAATATTTT	114804
rs760955765	snp	A/C	1.65575e-05	0.00287724	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167059	GGGAGGGCAGGCAGA[A/C]CTGCTGACACACTCC	114804
rs760983054	snp	G/T	3.29533e-05	0.00405901	missense, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154294	CCACCTTCCTGCGTG[G/T]GTGATCCATCCTCTT	114804
rs761026414	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76224104	GGCAATTTTTGAAGC[A/G]AAAGCCCAAAATCAA	114804
rs761045592	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76232312	AGGAGTGCCTGAGCC[C/T]AGTAGGTCGACGCTG	114804
rs761050252	in-del	-/TTTC			intron-variant	RNF157	GRCh38.p7	17:76168249	CTATGGAAACAAGGA[-/TTTC]TTTCTCTTTCCTCAC	114804
rs761089704	snp	A/G			intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154145	TGATGTACCATTAAG[A/G]AGACGATCTTTCCTC	114804
rs761098496	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76182965	GTTACTTTTCGCTCT[C/T]GTTGCCCTGGCTGGA	114804
rs761115380	snp	A/G	0.000166268	0.00911626	intron-variant	RNF157	GRCh38.p7	17:76167833	CATTTGCAGAGTAGC[A/G]TATCAATATTTTAAA	114804
rs761161537	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76234118	GGCATTTCTTATAAA[C/T]GAGATTATTCAATAG	114804
rs761162324	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76210384	GGATCACGAGGTCAG[A/G]TCGAGACCATCCTGG	114804
rs761215279	snp	C/T	4.52141e-05	0.00475447	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76173746	ATTGACCAGGCTTCT[C/T]AGAGTCTTCACGGGT	114804
rs761226500	in-del	-/TT/TTT			intron-variant	RNF157	GRCh38.p7	17:76163190	CTTGGCCCTGTTTCC[-/TT/TTT]TTTTTTTTTTTTTTT	114804
rs761250095	in-del	-/CT			intron-variant	RNF157	GRCh38.p7	17:76169279	TTTCATTTCTGCTCC[-/CT]CTGTTTTTAATTTCT	114804
rs761264909	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76201988	TTGGGCCAAAGGGTA[C/T]GCACAGCTCAAAATT	114804
rs761267676	snp	A/G	1.64746e-05	0.00287002	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161575	TGGGATGAGATGATG[A/G]GGTTAAAGCTGGTTG	114804
rs761268287	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76198715	CTTCATCTGAGAGAT[A/C]TTTTAAAATGTGTCT	114804
rs761270549	snp	A/G	1.66139e-05	0.00288213	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76162608	TCTCCTGAAGGAGGT[A/G]GCTGACCCCGTCTAC	114804
rs761302187	in-del	-/GAA	1.64917e-05	0.00287151	intron-variant	RNF157	GRCh38.p7	17:76165571	CAAAGGCACGTGAGT[-/GAA]GAAGCCCAAACAGCA	114804
rs761337660	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76227647	GTTTGGGAGGCCGAG[A/G]TGGGCGGATCACCTG	114804
rs761375827	snp	G/T	1.68732e-05	0.00290454	intron-variant	RNF157	GRCh38.p7	17:76159617	TTAATTAGGTCCTTT[G/T]TGTTTTATGACGTGA	114804
rs761383797	snp	A/G			intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76155000	AGGGGCTGGCCAGAA[A/G]AGTTCCCTCTTGAAC	114804
rs761408862	snp	A/G			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146232	GCAGTGTGACCTTGG[A/G]CACATCAGTTTACTG	114804
rs761410443	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76225478	TTTATACATATACAA[A/G]TATGTCCAGGTCTTC	114804
rs761460721	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76187944	AAAGATGTGCGGAAA[C/T]CCTAATGGAAAAATC	114804
rs761507935	in-del	-/TGAT	1.64855e-05	0.00287097	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154381	GCAAAATGAGTAAAC[-/TGAT]TGGCTGAAGACAGAA	114804
rs761536822	snp	C/G	1.65179e-05	0.00287379	intron-variant	RNF157	GRCh38.p7	17:76158384	GAAGAGGAGAGGAAT[C/G]TCAATTACCTCTCCG	114804
rs761569954	snp	C/T	1.65364e-05	0.0028754	intron-variant	RNF157	GRCh38.p7	17:76158362	GTCCCTGGAGTACAA[C/T]ACCCAAGAAGAGGAG	114804
rs761580440	snp	A/G	1.64817e-05	0.00287064	synonymous-codon, intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152401	GTCCAGTGCTTTCAC[A/G]CTTGCGATGTCAAAG	114804
rs761604712	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76221665	CTTCTAAAATAACTA[-/T]TAAGAAATAAAATAC	114804
rs761609315	snp	C/T	1.64871e-05	0.00287111	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76166476	CGTCTCCTTCATCCA[C/T]CACGGCATGTACCAC	114804
rs761647635	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76194111	TAAAATTCAGCCTTT[C/T]TGGTGTACAGTTCTG	114804
rs761666884	snp	A/C	4.45682e-05	0.0047204	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76240229	GTGCTGCCGGCTCGT[A/C]AGGGCCCCCATGGCC	114804
rs761722047	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76239476	ACTACGCTAGCAAAG[C/G]GGCAATCCGAGTAAC	114804
rs761726958	in-del	-/AT			intron-variant	RNF157	GRCh38.p7	17:76185978	AAAAATATAAAACAT[-/AT]ATATATATATATTTC	114804
rs761741928	snp	C/T	1.64762e-05	0.00287016	missense, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154314	TCCATCCTCTTCCTC[C/T]ATAACATCATTTCCC	114804
rs761775134	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76168970	CTGTTGATCCTTCTT[C/T]TTCTGAAAGCTTACA	114804
rs761786557	snp	C/T	3.30437e-05	0.00406457	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152472	TCCTCTGGCCTGTAA[C/T]GGAGTTAATGCAGTT	114804
rs761797039	snp	A/G			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213345	GAGGCTGAGGAGGGC[A/G]GATCACTTGAGGTCA	114804
rs761862074	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76185771	ACCGCGCCCGGCCGA[C/G]ATTACTCCTTTCACA	114804
rs761928768	snp	A/G	3.29804e-05	0.00406068	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159387	TGCTGTCAGACAGGC[A/G]GTCAAGAGGCGAGAT	114804
rs761930102	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76218346	GAGGAGTCTACTAAG[G/T]AATAAGCTTCCAGGC	114804
rs761962695	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76184684	CAGCTTAGAATGAAT[A/G]GTAATCACAAAGCTG	114804
rs761976279	snp	C/T	1.65776e-05	0.00287898	intron-variant	RNF157	GRCh38.p7	17:76167162	CAAAGCAAAAGTCAG[C/T]ATCCGGCACAGATGG	114804
rs762021841	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76197549	ATGATAGTCAGTAAG[C/G]TTCCTTTGGCAATTT	114804
rs762029318	snp	A/G	1.64735e-05	0.00286993	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76167695	GGCCTGGTAATAGAT[A/G]GTGATGGCTACCCGA	114804
rs762073409	in-del	-/AGAA			intron-variant	RNF157	GRCh38.p7	17:76230883	GAGAGAGAGAGAAAG[-/AGAA]AGAGAGAAAGAGAGA	114804
rs762100769	snp	C/T	5.0374e-05	0.00501841	intron-variant	RNF157	GRCh38.p7	17:76161793	TGTTTTGTAAATGTC[C/T]TCTTGTCCCCTCTCC	114804
rs762102358	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76235477	TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC	114804
rs762215338	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76163657	TAAGACATAGCCTGT[C/T]GCTGATTTTATATCC	114804
rs762236007	snp	A/G	3.30142e-05	0.00406276	intron-variant	RNF157	GRCh38.p7	17:76212324	TTTTTTGAATTGGCC[A/G]CTTAAGCTCCAAGTA	114804
rs762244824	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76196132	AGCAGTCACAGAGCT[G/T]TAACACTGCCGCCTC	114804
rs762257100	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76164952	ACTGTCTGAAAATAT[G/T]ACATACAATATTTTG	114804
rs762303367	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76176150	GAGTAAGGAGAGATT[A/G]AAAACCAAGAAGATA	114804
rs762319186	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76222755	ACTCCACATCTCAAC[A/C]CTGCACCTGTCTCTC	114804
rs762321215	snp	C/G	1.66374e-05	0.00288417	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76164759	TTACTACTTGTTTCT[C/G]TTTGAGGGGCTTGAC	114804
rs762323446	in-del	-/A			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149596	AGAGAGTTCTCCAGC[-/A]AAATTTTCTGCCAGT	114804
rs762329083	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76160676	TTGTAAATAGTTTTT[-/A]AAAAAAACACTATTT	114804
rs762354221	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76219340	ACATATAAATATAAC[A/G]TAAAATGGCCAGCCT	114804
rs762397986	snp	A/G			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213003	CCAGATACCAAACGT[A/G]GACTAGATCACTGTT	114804
rs762426180	in-del	-/CTT	1.68343e-05	0.00290118	cds-indel, nc-transcript-variant	RNF157	GRCh38.p7	17:76155567	CTTCCCTTACCTCTC[-/CTT]CTTCTGAGGGGGCCC	114804
rs762433024	snp	A/G	4.98708e-05	0.00499328	intron-variant, downstream-variant-500B	RNF157	GRCh38.p7	17:76156197	ATGCAGCCACTCCCC[A/G]CTCCTTATGTACCTT	114804
rs762441817	snp	C/T	1.66676e-05	0.00288679	intron-variant	RNF157	GRCh38.p7	17:76158540	AGCTATATCCAACGT[C/T]CATTTAAAGAACAGA	114804
rs762462758	in-del	-/C			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76152049	GAAAACAAGACTGGG[-/C]CACCTGACATGGTAC	114804
rs762466677	snp	A/G	3.08609e-05	0.00392804	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76155712	GGACATGACAGACTG[A/G]GCCAAGCTGCTGCTG	114804
rs762479554	in-del	-/TG	1.68764e-05	0.00290481	frameshift-variant, nc-transcript-variant	RNF157	GRCh38.p7	17:76162562	CTTACCTTAGAATCT[-/TG]TGTGTTGTACTTGTT	114804
rs762488130	snp	A/G	6.91778e-05	0.00588083	synonymous-codon, intron-variant, utr-variant-3-prime, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145241	GGCTGGGGCTCAGAC[A/G]GCCAAAGGGCCCCAC	114804
rs762492987	snp	A/G	1.67161e-05	0.00289098	intron-variant	RNF157	GRCh38.p7	17:76161685	TCAGGACATCCTGAT[A/G]CAGGATTAAGAATGA	114804
rs762540592	snp	A/G	1.64838e-05	0.00287083	intron-variant	RNF157	GRCh38.p7	17:76212341	TTAAGCTCCAAGTAG[A/G]AGTAAACTGATTACA	114804
rs762543408	snp	A/G			missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155704	GATGCCATGGACATG[A/G]CAGACTGGGCCAAGC	114804
rs762595082	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76200750	AAGCCCTAAACCATT[C/T]TAAAAGTATGAATAT	114804
rs762603927	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76156859	GTGCACAGCCTCACC[C/T]GTCCAAGATGGATGC	114804
rs762664660	snp	A/G	1.65318e-05	0.002875	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152484	TAACGGAGTTAATGC[A/G]GTTAGAGAGGGGCTG	114804
rs762666470	in-del	-/AG			intron-variant	RNF157	GRCh38.p7	17:76199133	AGTGATTTGTGTAAC[-/AG]AGAGGGGAAAGAAGA	114804
rs762697608	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76168680	TTTTGCCTCTGTCCT[C/T]CTGTAGAAGCTCATG	114804
rs762744482	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76238500	GTCTTTTTATTATCA[C/T]CACCCAAGATTCATA	114804
rs762752481	in-del	-/C			intron-variant, upstream-variant-2KB, downstream-variant-500B	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142274	CCAGGAGCTGGAGAG[-/C]CGGGGTCGGGGAGGC	114804
rs762792511	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76191291	GATCGGTTAGGGCAA[C/T]ATAGTGAGACACCGT	114804
rs762842773	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76186495	CTGAGCAACAAGAGT[A/G]AGACTCTGTCTCAAA	114804
rs762940847	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76228118	AAAAAAACCATTTAT[A/G]GAATATTCCATTTCC	114804
rs762941881	snp	A/G	1.64735e-05	0.00286993	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76167710	GGTGATGGCTACCCG[A/G]GCATCTGTGTCAAAG	114804
rs762991219	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76192970	TGAGTAACAGCCGCG[C/T]GCCACCACACCTAGC	114804
rs762996898	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76228873	AGGTTGCAGTGAGCT[A/G]AGACTGCGCCATTGG	114804
rs763056397	snp	A/C	1.66172e-05	0.00288242	intron-variant	RNF157	GRCh38.p7	17:76155330	CCCCTGCAGAAGAGC[A/C]CAGTTTTTACAGGCT	114804
rs763069315	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76230189	AATCCACAGAAACCT[C/T]TGAGGGGGCATTAAA	114804
rs763071977	snp	A/G	0.000230741	0.0107386	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161884	GCCTGGTAGCGCAGC[A/G]TGTCTGCACAGGTGT	114804
rs763188843	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76181389	TCTAAGGTCTTCTTA[A/G]AGAAGAGCTTTCTTG	114804
rs763190960	snp	A/T	0.000221735	0.010527	intron-variant	RNF157	GRCh38.p7	17:76162021	GCCAAGGAGAAAGAA[A/T]TGTAGCCAATGGCAC	114804
rs763206648	snp	G/T			upstream-variant-2KB	RNF157	GRCh38.p7	17:76241604	TTTCCTGGTTATATT[G/T]TGTTTTTGTTTTTCT	114804
rs763208297	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76187809	TACCATGTTGGTCAG[G/T]CTGCTCTTGAACTCC	114804
rs763212347	snp	A/G	1.66021e-05	0.0028811	intron-variant	RNF157	GRCh38.p7	17:76159298	AGCATTTCATCAAGG[A/G]TTCCGGGGGCAACAG	114804
rs763296176	snp	A/G			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146060	CTGCTGCCCCCACAT[A/G]AGGAGTGCCAGCGCC	114804
rs763321650	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76183168	TCTCGAACTCCTGAC[C/T]TCAGGCGATCCGCCC	114804
rs763342940	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76174959	AGTTTTTTCTAATTA[C/T]AAAGTAATATATGTT	114804
rs763361273	snp	A/G	0.000461593	0.015185	intron-variant	RNF157	GRCh38.p7	17:76165457	GTGTCTCACACGAAA[A/G]AAAGGGCTAAAGGCA	114804
rs763380216	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76208142	TGCCCAGGCTGGTTT[C/T]CAATTTCTAGGCTCA	114804
rs763388468	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76176070	GGGCTGCTACCCACC[A/T]AAGTTTGTGCCTTGC	114804
rs763392536	snp	A/T	1.64985e-05	0.0028721	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76159487	AAGCACGTGAAGTGG[A/T]GGAACTGCTGGGGAC	114804
rs763412468	snp	A/G	1.64912e-05	0.00287147	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159395	GACAGGCGGTCAAGA[A/G]GCGAGATCGTCCTGA	114804
rs763419126	in-del	-/GG			intron-variant	RNF157	GRCh38.p7	17:76197753	AGCATTTAAAGACAA[-/GG]TCATTTCCTGCAGGC	114804
rs763420469	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76222518	AGTCAGGTTATAATG[C/T]TGTCATTTGAATTTT	114804
rs763428910	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76187049	GAAATAGTTAAGTTT[A/G]TAAGCCAAACAAACA	114804
rs763457258	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76233941	CGTGTTATACAACTA[C/T]TCACCACTATCTAAT	114804
rs763483698	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76163452	CACCTGCCTCAGGCT[C/T]CCGAACTGCTAGGAT	114804
rs763575822	snp	C/T	1.65051e-05	0.00287267	intron-variant	RNF157	GRCh38.p7	17:76155242	CACCACTCCGTGCTG[C/T]TGGGGTTACCTCTGC	114804
rs763601064	snp	C/T			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213164	ACTTGAAGTAGTTAT[C/T]CCATGTATTGAAGAA	114804
rs763606879	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76155763	GGATGGGGAAAGGAG[C/G]CTGGAGGTCAGGCAG	114804
rs763617415	snp	C/T	1.65307e-05	0.0028749	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76159514	GGACGGGGTGAGGGG[C/T]CCGTTGAGGGCCTCC	114804
rs763672842	snp	A/G	3.37992e-05	0.00411077	intron-variant	RNF157	GRCh38.p7	17:76155516	CTACTTTGGACATGT[A/G]CACAAAGAACAGAGA	114804
rs763689950	in-del	-/A			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76152102	GAGAGTGGTTAGGCC[-/A]AAATCGTTAAGTTTT	114804
rs763738132	snp	A/G			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76144987	ACATCAATATACCGT[A/G]AGGACATTCCAGAGT	114804
rs763789780	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76219770	ACTGTAATTTAACTG[C/T]ACATCTCAATAGGAA	114804
rs763795110	snp	C/G	1.67621e-05	0.00289495	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155597	CCCTGCTGGCAGGCT[C/G]GGGGGAAGAGAGAGC	114804
rs763797296	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76200838	ATCTCATACCATTTC[A/G]AATCAACTGTTTCTA	114804
rs763839965	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76209448	CCCAACAGAAACTCG[-/T]AAACTTTCTTAAAAC	114804
rs763912756	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76178494	AGTCTCCCTTGGAGG[C/T]GTGGGATATAGGCTG	114804
rs763921410	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76166871	CAGAGCTTTAAAAGG[A/C]CATGATGAAGTCACA	114804
rs763922295	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76160739	GACCTCTGAAGTGCT[A/T]AACTTTTTAGGTGGT	114804
rs763923581	snp	A/G/T	0.000104209	0.00721773	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76240208	GTCCACCTCCTCCAC[A/G/T]CCCGCGTGCTGCCGG	114804
rs763928767	snp	C/T	1.65594e-05	0.0028774	missense, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156299	AAGGTGAGATTCTCA[C/T]TTTCTGGAGTCACAC	114804
rs763938262	in-del	-/A			utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142734	CAGGCCAGCCGGCTT[-/A]AGAGTGTGGTGGTCT	114804
rs763953349	snp	C/T	1.72749e-05	0.0029389	intron-variant	RNF157	GRCh38.p7	17:76240102	TCCCGACCCAGACCC[C/T]TGCCCCTGCCCCTCT	114804
rs763980606	snp	C/T	4.94572e-05	0.00497254	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76166464	AATCGCCCCTACCGT[C/T]TCCTTCATCCACCAC	114804
rs763993789	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76212132	AGAGATCTGTCCTAG[C/T]TTAATTTGTGAGACT	114804
rs764003241	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76226081	TGGGAGGCTCCTATT[C/T]GGAGAGCCCCTGGTA	114804
rs764015244	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76191432	CCTGGCCAAAACCCT[A/G]TCTCTACTAAAAATA	114804
rs764053397	snp	C/G	3.66656e-05	0.00428153	missense, intron-variant, utr-variant-3-prime, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145347	TTGTCATCAGCCTGC[C/G]AGGCACCTGGGGAAG	114804
rs764065901	snp	C/G			intron-variant, upstream-variant-2KB, downstream-variant-500B	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76141973	TCACTCCTCTGGAGA[C/G]AGCTGATGAAGCAGA	114804
rs764079854	snp	C/T	3.29804e-05	0.00406068	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76165527	GTACCCAGCAGTACA[C/T]GGCAATGGCCAAAAT	114804
rs764089778	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76181437	ATCTTTGTCTATAAG[A/G]TCTAACAGTACCTGC	114804
rs764089998	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76180035	GCATCCTGGCATATC[C/T]GGAAACAGGAAGAGC	114804
rs764091291	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76228567	TCATCCTACAAGCAT[A/G]TACTGGTCTCCCCAA	114804
rs764099471	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76196053	GTGGGTATAAATATG[A/G]TTACAAACCTGCTCT	114804
rs764111772	in-del	-/CTCT			intron-variant	RNF157	GRCh38.p7	17:76190166	GGCTAACTGCTTGCT[-/CTCT]CTTTTTTTTTTTTTT	114804
rs764163419	snp	C/G	1.65537e-05	0.0028769	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167062	AGGGCAGGCAGAACT[C/G]CTGACACACTCCTCG	114804
rs764183727	snp	A/C	1.64762e-05	0.00287016	missense, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154300	TCCTGCGTGGGTGAT[A/C]CATCCTCTTCCTCTA	114804
rs764214050	snp	A/G	1.65526e-05	0.00287681	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152503	AGAGAGGGGCTGGCT[A/G]TGTTTTTCTCTGCGT	114804
rs764285877	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76215348	GGCATGGTAGCATGC[A/G]TCTGGAGTTCTAGCT	114804
rs764311286	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76204215	ACACTTCTGCATCTT[-/T]ATGCTTCCTTGTATT	114804
rs764317675	snp	C/T			intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153349	CTTGGCGGCCACCTT[C/T]TCCTTCAAGCTCCTT	114804
rs764394077	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76175081	TCTCCATCCGTCCGT[C/G]TATCCATCCATCCTG	114804
rs764442742	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76230250	TGGGTTTCTGTCTAA[C/T]TTCCCCGGATCTTGA	114804
rs764461259	in-del	-/T	1.65134e-05	0.0028734	frameshift-variant, nc-transcript-variant	RNF157	GRCh38.p7	17:76158394	GGAATGTCAATTACC[-/T]CTCCGAGATGCTGAA	114804
rs764463110	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76173843	AAAAAGACCCACAGC[A/T]GTCCCTCGCTTTACA	114804
rs764493128	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76162297	GATCACACAGATAAA[A/G]GAAAAGGAGCAAAGA	114804
rs764504618	in-del	-/AA	0.000133877	0.00818049	intron-variant	RNF157	GRCh38.p7	17:76166437	GCAGTGTGCACAGCC[-/AA]AGAGGACAGAAATCG	114804
rs764585127	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76143346	CTTCCTCCCTCCTCC[C/T]AGGTAACACCACACT	114804
rs764629325	snp	A/C	1.67072e-05	0.00289021	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155612	GGGGGGAAGAGAGAG[A/C]CTCTCCCTCCTCTTC	114804
rs764688768	in-del	-/G			intron-variant	RNF157	GRCh38.p7	17:76225487	ATACAAATATGTCCA[-/G]GTCTTCCTGTTCTAT	114804
rs764689805	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76173285	GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAGAAA	114804
rs764706435	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76199090	TGTAAATGATTGAGG[A/G]AATAATGAAGGAGTG	114804
rs764727533	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76225892	GCACTCGCCAGTGAG[A/G]GCCTCCTGCTCCGCC	114804
rs764759788	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76232140	GTAATTCCTGCACTT[C/T]GAGAGGCCGAGGCTG	114804
rs764779464	in-del	-/TC			intron-variant	RNF157	GRCh38.p7	17:76202113	CCCAATCTCAGTTTC[-/TC]TCTCTCTCTCTCTCT	114804
rs764827180	in-del	-/TG			intron-variant	RNF157	GRCh38.p7	17:76232139	GTAATTCCTGCACTT[-/TG]TGAGAGGCCGAGGCT	114804
rs764846040	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76178399	TGCCAGCCCCACAGC[A/G]GCAGCTGGCGTGTCT	114804
rs764862583	in-del	-/CA	1.65939e-05	0.0028804	intron-variant	RNF157	GRCh38.p7	17:76155329	GCCCCTGCAGAAGAG[-/CA]CAGTTTTTACAGGCT	114804
rs764875177	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76155155	GAAGGCTTCGTCAGC[A/G]CAGCCTCCTGGCCCT	114804
rs764890495	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76159318	GGGGGCAACAGTGTG[C/G]AGCACTGGCTACTCA	114804
rs764901300	snp	C/T	0.000221596	0.0105237	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155693	TGATCTGGGAGGATG[C/T]CATGGACATGACAGA	114804
rs764985284	snp	C/G	1.66835e-05	0.00288816	intron-variant	RNF157	GRCh38.p7	17:76162629	CCCCGTCTACCTGAA[C/G]AGCAAACAGAAAGGT	114804
rs764995890	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76198154	CAAAGAGAGGAGAGG[C/G]CTTATCATGCCAGAG	114804
rs765032397	snp	C/T			intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76148741	AAGCCTGGCTAATTT[C/T]TGTATTTTCTGTAGA	114804
rs765048782	snp	C/T	3.2963e-05	0.00405961	missense, intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152402	TCCAGTGCTTTCACG[C/T]TTGCGATGTCAAAGT	114804
rs765056190	in-del	-/TCTTT			intron-variant	RNF157	GRCh38.p7	17:76190169	TAACTGCTTGCTCTC[-/TCTTT]TTTTTTTTTTTTTGA	114804
rs765063608	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76189588	AGGTATTTTAATAGG[C/T]AGAATTAAATACAAG	114804
rs765074952	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76177248	AACAGGCAGCAGCCC[C/T]GCCTTGGGCTGTGGA	114804
rs765118405	snp	A/C	1.66394e-05	0.00288434	intron-variant	RNF157	GRCh38.p7	17:76158533	GAAAAGCAGCTATAT[A/C]CAACGTCCATTTAAA	114804
rs765151336	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76203021	TTTTTTGAGAGAGGG[A/T]CTCGTCCAGCCCAGG	114804
rs765156765	snp	C/T	0.000152046	0.0087178	intron-variant	RNF157	GRCh38.p7	17:76159623	AGGTCCTTTTTGTTT[C/T]ATGACGTGATCATGC	114804
rs765167356	snp	C/T	0.000165503	0.00909527	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76159529	CCCGTTGAGGGCCTC[C/T]AGAAGAGATACTACT	114804
rs765167640	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76182611	GGACATCTTACTCTG[C/T]GTGTAAATTATTAGG	114804
rs765184655	in-del	-/T			utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76143761	GGAAACAGCCTTGAA[-/T]TTTTTTTTTTTTTGT	114804
rs765241993	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76194732	ATAAAACCACAAGAG[C/T]AGGCCGGGCACGGTG	114804
rs765389219	snp	C/T	1.67778e-05	0.00289631	intron-variant	RNF157	GRCh38.p7	17:76161799	GTAAATGTCCTCTTG[C/T]CCCCTCTCCCACCCA	114804
rs765445735	snp	C/T	1.6525e-05	0.00287441	synonymous-codon, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156232	GGAGGAAATAGTGGA[C/T]GACAGAGGCGTCCCT	114804
rs765457771	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76162174	CACTTAGCTTCACTT[C/T]TTCTGGGAAGTGTTT	114804
rs765500407	snp	A/G			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153035	TTCAGTGTGTTTTAA[A/G]TGGCTAACCAGAAAT	114804
rs765509853	snp	A/G			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213755	CCCCAACCACTGAGG[A/G]AGGGAGAGGGGATGA	114804
rs765531438	snp	A/G			upstream-variant-2KB	RNF157	GRCh38.p7	17:76242289	TGCCTTATGCTCCTC[A/G]GCTCTGTTCAGAAGC	114804
rs765535900	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76218489	CTACAATAAAAAAAT[C/T]AAAAAGTTAGCCAGG	114804
rs765545000	snp	C/G			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76144962	GCCCATGGACCCCAG[C/G]TCCACCTGAACATCA	114804
rs765545866	snp	C/G	1.66535e-05	0.00288556	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76164774	GTTTGAGGGGCTTGA[C/G]ACAGAAAGTTCCATC	114804
rs765581195	in-del	-/A	0.00146806	0.0270531	intron-variant	RNF157	GRCh38.p7	17:76166551	AAAGAAAAGGAAAGG[-/A]AAAAAAAAGAGGACT	114804
rs765637183	snp	A/T	3.64571e-05	0.00426933	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155657	TGTAGGAGCCAGACA[A/T]GGAGGAGACGGTGTC	114804
rs765770744	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76161180	ACAGTTACTTTCTTC[A/G]AGGATTCAAATAAAG	114804
rs765774428	snp	A/G	1.67329e-05	0.00289243	intron-variant	RNF157	GRCh38.p7	17:76158550	AACGTCCATTTAAAG[A/G]ACAGAACTTACTGCA	114804
rs765819133	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76176946	CGGGAGGAGGTTCTG[C/T]GCAGCCCGTCTGGGG	114804
rs765839728	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76174795	ATCTGACTTAATGTA[C/T]GCAGTATAATTGCTT	114804
rs765846586	in-del	-/A	1.64928e-05	0.00287161	intron-variant	RNF157	GRCh38.p7	17:76165457	TGTCTCACACGAAAG[-/A]AAAGGGCTAAAGGCA	114804
rs765891117	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76236784	CAGAGGAATACTATA[C/T]AGTTGTTAAAAAGCA	114804
rs765902899	snp	A/G	8.23784e-05	0.00641735	synonymous-codon, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154320	CTCTTCCTCTATAAC[A/G]TCATTTCCCTAGGAC	114804
rs765905427	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76176410	GACAGTAGGATCAGA[A/G]GCAAATTAAAAAAAA	114804
rs765928051	snp	A/G/T			intron-variant	RNF157	GRCh38.p7	17:76210389	ACGAGGTCAGATCGA[A/G/T]ACCATCCTGGCTAAC	114804
rs765934884	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76189404	ATGAGCAGAAGGCGT[A/G]GGTCTCAGCTCCTGT	114804
rs765953783	snp	C/T	1.65927e-05	0.00288029	intron-variant, downstream-variant-500B	RNF157	GRCh38.p7	17:76156202	GCCACTCCCCGCTCC[C/T]TATGTACCTTCTGGG	114804
rs765957714	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149836	GTCAGGAGTTCAAGA[C/T]CACCCTGACCAACAT	114804
rs765996279	snp	C/G/T	3.33897e-05	0.00408582	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76164782	GGCTTGACACAGAAA[C/G/T]TTCCATCTGTGTGCT	114804
rs766004312	snp	A/C	6.90918e-05	0.00587717	missense, intron-variant, utr-variant-3-prime, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145255	CAGCCAAAGGGCCCC[A/C]CACACAGGGCCTCGT	114804
rs766011368	snp	A/G	4.94686e-05	0.00497311	intron-variant	RNF157	GRCh38.p7	17:76165462	TCACACGAAAGAAAG[A/G]GCTAAAGGCAATAAA	114804
rs766015828	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76165193	GGATAAGGGGGGACT[A/C]CTGTACACATGTTCC	114804
rs766016413	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76224790	CTAATTTGTGTTGCG[C/T]TGCATTCAAAGCCAT	114804
rs766043299	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76170886	TTAAAGAAATTTTTA[A/C]AATTTTTTATTTATT	114804
rs766046818	snp	C/T			intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76148358	TGCAAGCTCCGCCTC[C/T]CGGGTTCACGCCATT	114804
rs766123438	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76209594	AGGGAACCCAAAAGA[C/T]TGGACATCCCTGATT	114804
rs766215347	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76186537	AACGAAACAAAAAAA[A/C]CCCAAAAAAACTACT	114804
rs766217911	snp	G/T	1.65734e-05	0.00287862	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167050	CCACGGTGTGGGAGG[G/T]CAGGCAGAACTGCTG	114804
rs766224408	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76225641	TGACCTCATTGTTTT[C/T]AGTGGCCAAATAATA	114804
rs766236615	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76169404	GTTTTCTTCTTCCTG[A/C]ATAGCTTTTGTTTCC	114804
rs766237504	in-del	-/TTTTT			intron-variant	RNF157	GRCh38.p7	17:76205134	TCCTCTTTTCTTTTC[-/TTTTT]TTCTTTCTTTTTTTT	114804
rs766267436	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76235179	GCCAACCAAATAATT[C/T]CTTATTTTGTAGTAG	114804
rs766284191	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76202203	CCCGTTCCCACCATG[A/G]GCTTTAGGCCTGTAG	114804
rs766308159	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76202810	ATTGGTCCATGGTTC[C/T]AGGGTAGAAAGTCTG	114804
rs766312263	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76199594	AAAAAAAAAAAAAAG[A/G]ACAGCTGGCAGGAAG	114804
rs766312503	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76228303	GTCCCAACCCCAACC[C/T]TGTACCCTTCTTCCT	114804
rs766323399	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76160978	TGAAATAGCTAACTA[A/G]TTATCCCAATACCAT	114804
rs766349107	snp	G/T	4.53535e-05	0.0047618	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76173762	AGAGTCTTCACGGGT[G/T]CTTGGGGAGGTGGGG	114804
rs766411234	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76173555	CTCAGCAGAAAGTAG[C/T]GCCCGCACTCCTGTC	114804
rs766453306	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76205815	GCATGAGGAAGAAGA[A/C]ACTGTGTCAATGCGG	114804
rs766453752	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76219421	ATTATGCTACCATGT[A/G]TGTAAGGAAGAGTGG	114804
rs766465940	snp	A/G	1.64787e-05	0.00287038	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161924	AGAGGTGGCGACAGG[A/G]CAGAATCAAGGTGTC	114804
rs766478237	snp	A/G	3.13642e-05	0.00395994	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155713	GACATGACAGACTGG[A/G]CCAAGCTGCTGCTGG	114804
rs766517484	snp	G/T	0.0264403	0.111898	intron-variant	RNF157	GRCh38.p7	17:76162023	CAAGGAGAAAGAAAT[G/T]TAGCCAATGGCACAA	114804
rs766567177	snp	C/G	1.85283e-05	0.00304365	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145370	TGGGGAAGAGAAAAT[C/G]AACATTACAGGAGCC	114804
rs766597079	snp	A/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151143	CCTCCACGCTCAGGC[A/G]GGAAGGGGGTCTTCC	114804
rs766615851	snp	G/T			intron-variant, upstream-variant-2KB, downstream-variant-500B	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142019	TCTGAAGTCATGGAC[G/T]TGTCAAATTCTCCTA	114804
rs766626265	snp	C/T	4.9476e-05	0.00497348	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76159397	CAGGCGGTCAAGAGG[C/T]GAGATCGTCCTGACG	114804
rs766644323	snp	A/T	1.65168e-05	0.00287369	intron-variant	RNF157	GRCh38.p7	17:76158385	AAGAGGAGAGGAATG[A/T]CAATTACCTCTCCGA	114804
rs766700791	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76183240	CCACGCCCGGCCTCA[A/C]GTGGGAATATTTTTG	114804
rs766707789	snp	C/T			intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154152	CCATTAAGAAGACGA[C/T]CTTTCCTCTAACAGC	114804
rs766753794	snp	C/G	4.61095e-05	0.00480132	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76240231	GCTGCCGGCTCGTCA[C/G]GGCCCCCATGGCCGC	114804
rs766755997	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76238771	TATTTTTGTCTATTA[A/C]AAAACAAAATCTATG	114804
rs766782769	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76183079	AGCTGGGATTACAGG[C/T]GTCTGCCACCATGCC	114804
rs766787606	snp	G/T	4.97847e-05	0.00498897	intron-variant	RNF157	GRCh38.p7	17:76167177	TATCCGGCACAGATG[G/T]GTCTGACAACTTCCT	114804
rs766791025	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76198732	TTTAAAATGTGTCTT[C/T]TGTGAGCCCCAGTTT	114804
rs766806685	snp	G/T			missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76164778	GAGGGGCTTGACACA[G/T]AAAGTTCCATCTGTG	114804
rs766826556	snp	C/T	1.64776e-05	0.00287028	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154349	ACAGAAGGAAGGCCC[C/T]GTGAGTCTATGAAGC	114804
rs766881956	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76197768	ATCATTTCCTGCAGG[C/T]ACAAGACCTAATTTT	114804
rs766894651	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76172311	AAAGTGAGACTCTGG[C/G]CCAGGTGCGGTGGCT	114804
rs766953613	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76232052	TTTTGAAGTTAAATC[A/G]TGTTGTATAGCATGT	114804
rs767017120	snp	C/G			intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146309	TCACGGGCTTGCTGT[C/G]AGGACTAGATGAGAG	114804
rs767041574	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76234149	ATGGCCTTTTGCACC[G/T]GGCTTATTTCACTGA	114804
rs767086581	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76201992	GCCAAAGGGTACGCA[C/G]AGCTCAAAATTTAAT	114804
rs767087905	snp	A/G	1.64923e-05	0.00287156	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159404	TCAAGAGGCGAGATC[A/G]TCCTGACGGGGGGCA	114804
rs767108083	in-del	-/TGTC			intron-variant	RNF157	GRCh38.p7	17:76200329	CAGGAGCAACCCAAG[-/TGTC]TGTCTATTGATGGAT	114804
rs767132432	snp	A/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149929	ATCCCAGCTACTCAG[A/G]AGGCTGAGGCAGAGA	114804
rs767141044	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76176162	ATTGAAAACCAAGAA[A/G]ATAAGGCCCTGCTCT	114804
rs767144980	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76161338	AAGTTCCCAAGGAGG[-/A]AAAAGGGAGGTTTTC	114804
rs767179185	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76228794	GGCGTGGTGGTGGGC[A/G]CCTGTAATCCCAGCT	114804
rs767226620	snp	A/G	1.65138e-05	0.00287343	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159500	GGAGGAACTGCTGGG[A/G]ACGGGGTGAGGGGCC	114804
rs767321100	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76221423	ACATGATTAATGAGA[C/G]TTCAAGGAGGCAACT	114804
rs767361468	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151703	AGGCATTACCTAGAT[C/T]TGGTTTAGCATCATG	114804
rs767362051	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76167517	CTGAGTGGATAAGAC[A/T]TGGACTCTCCCTATC	114804
rs767368705	snp	A/C/G	5.0387e-05	0.0050191	intron-variant	RNF157	GRCh38.p7	17:76161699	TACAGGATTAAGAAT[A/C/G]AACAAGAGCCCAGAC	114804
rs767394977	snp	A/G	4.31304e-05	0.00464363	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76155730	CAAGCTGCTGCTGGC[A/G]GGGCCTTTGGAGACA	114804
rs767395846	snp	C/T	1.71299e-05	0.00292654	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212508	ACAAACAAAAAAAAT[C/T]AAACAAGCAGAAAAC	114804
rs767422156	snp	C/T			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213488	GGCAGGAGAATCTCT[C/T]GAACCCGGGAGGCAG	114804
rs767524347	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76182608	AAAGGACATCTTACT[C/G]TGTGTGTAAATTATT	114804
rs767527055	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76172059	TCAGGTCGGGGGACT[A/G]TTCTGCAGCAGACAG	114804
rs767554386	snp	A/G			intron-variant, downstream-variant-500B	RNF157	GRCh38.p7	17:76156178	CTGGGTAAGGGGGAA[A/G]GACATGCAGCCACTC	114804
rs767560151	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76168985	CTTCTGAAAGCTTAC[A/C]GACGGTCCTCTTTCT	114804
rs767569280	in-del	-/T			utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76143188	GGTATGCCTTGGACA[-/T]GGGACTGAGGCCTTG	114804
rs767608093	snp	C/T	1.65124e-05	0.00287331	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76158398	TGTCAATTACCTCTC[C/T]GAGATGCTGAACCGA	114804
rs767623919	snp	C/T	2.28068e-05	0.00337682	synonymous-codon, intron-variant, utr-variant-3-prime, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145265	GCCCCACACACAGGG[C/T]CTCGTCTCAGAGTCC	114804
rs767675125	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76187301	CCATTCTCCTGCCTC[A/C]GTCTCCCGAGTAGCT	114804
rs767684454	snp	A/G	1.6483e-05	0.00287076	synonymous-codon, intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152416	GCTTGCGATGTCAAA[A/G]TCATTGTTATTGTCA	114804
rs767702270	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76203093	CCTTCTGGGTTCAAG[C/T]GATTCTTATGCCTCA	114804
rs767719100	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76159671	AAAAATGTTTTATAT[A/C]TGTTCTTGGGGGGGT	114804
rs767722975	snp	A/G			intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153427	CAAGCGATGGCCAGC[A/G]CTAAAGCAGAAGCAA	114804
rs767735794	snp	A/G	8.26631e-05	0.00642843	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152485	AACGGAGTTAATGCA[A/G]TTAGAGAGGGGCTGG	114804
rs767814221	in-del	-/GCTC			intron-variant	RNF157	GRCh38.p7	17:76190163	TCAGGCTAACTGCTT[-/GCTC]TCTCTTTTTTTTTTT	114804
rs767849383	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76218352	TCTACTAAGGAATAA[A/G]CTTCCAGGCCAAGCC	114804
rs767853978	snp	A/G	1.64825e-05	0.00287071	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161942	GAATCAAGGTGTCCC[A/G]GACATCCGAGAGACA	114804
rs767872077	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76164956	TCTGAAAATATTACA[C/T]ACAATATTTTGAGAG	114804
rs767880883	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76197615	AATATGGTACCCAGG[C/T]TTGGAGTGCAGTGGT	114804
rs767889910	snp	C/T	1.71678e-05	0.00292978	intron-variant	RNF157	GRCh38.p7	17:76166975	CTAGGCCCTTCTGAG[C/T]GGATGTGGGAAACCC	114804
rs767908068	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76176872	CTTCCGCTTCGGGCA[C/T]CTGGCCATTGGCGCA	114804
rs767929929	in-del	-/G	0.000108478	0.0073639	intron-variant	RNF157	GRCh38.p7	17:76155769	GGAAAGGAGCCTGGA[-/G]GTCAGGCAGGGCTTC	114804
rs767962907	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76230300	CCGACATTTAGGACT[C/G]ACTTCAAAAGCAGTT	114804
rs768001538	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76168743	GTTATTCTTTCATAT[C/T]GGTGGAGCACGTGTC	114804
rs768015947	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76210450	AAAAAATTAGCCGGG[C/T]GTAGTGGCGGGTGCC	114804
rs768042639	multinucleotide-polymorphism	AT/CC			intron-variant	RNF157	GRCh38.p7	17:76157114	TGGGACTACAGGTGC[AT/CC]GCCACCACACCTGGC	114804
rs768056450	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76227885	TCCATCTCAAAAAAA[A/G]TTTAAAAAAAGAGGT	114804
rs768078055	snp	A/G	1.65894e-05	0.00288	intron-variant	RNF157	GRCh38.p7	17:76167826	GACTCAGCATTTGCA[A/G]AGTAGCATATCAATA	114804
rs768099233	snp	A/C	4.94319e-05	0.00497127	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154253	AAAGAAAGATAACTA[A/C]AGGAAGTAAAGGACC	114804
rs768129802	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76196287	ACATTAAAGAGCAAA[C/T]TGAACACAGTTCCAC	114804
rs768130392	snp	A/G	3.32867e-05	0.00407949	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76167027	CTCTTCGGCCCACTC[A/G]GAGGGATCCACGGTG	114804
rs768135904	snp	A/G	3.45197e-05	0.00415435	intron-variant	RNF157	GRCh38.p7	17:76162049	CACAAAGCCCTTCCT[A/G]TCCCATACTTTACTG	114804
rs768224650	snp	A/G			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152555	CTTAAGGATGGAGAC[A/G]AAAAAAATCAAATCA	114804
rs768231378	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76180939	GTAAGTTCCGTGTGT[A/G]TGCTGGAGGACAGTC	114804
rs768238103	snp	A/G	0.000187548	0.00968189	intron-variant	RNF157	GRCh38.p7	17:76166552	AAGAAAAGGAAAGGA[A/G]AAAAAAAGAGGACTT	114804
rs768254641	snp	A/G	1.64743e-05	0.00287	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76161562	AGAGTCAGATGTCTG[A/G]GATGAGATGATGGGG	114804
rs768264671	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76160636	AACTATGGCAAAGAC[-/A]ATTAGCTTTTCCTCT	114804
rs768271517	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76201967	AGATTCGGAGAGGTG[A/C]AACAGTTGGGCCAAA	114804
rs768353128	in-del	-/G	1.65102e-05	0.00287312	intron-variant	RNF157	GRCh38.p7	17:76161507	GGCATTTGCTTCAGA[-/G]GGGGCCGTGGTTCCG	114804
rs768355686	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76214860	ATATGATGGAACTGA[A/G]AAGTCACCAAAGGAG	114804
rs768371176	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76206688	GCTCTTGTTGCCCAG[A/G]CTGGACTGCAATGGC	114804
rs768383653	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76174418	CTTCCCCCTTTGCCC[A/G]TTTAGACCTTTGGAT	114804
rs768402451	snp	A/G			missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161918	AGAGGCAGAGGTGGC[A/G]ACAGGGCAGAATCAA	114804
rs768414527	snp	C/T	2.94503e-05	0.00383722	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76173702	CCTCTGGGAACTTAC[C/T]TGACGAGCCTCAGTG	114804
rs768419137	in-del	-/AC			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147159	GGTGGCACTATGTGT[-/AC]CTAAGTGTGGCAGGA	114804
rs768420945	snp	A/G	1.69246e-05	0.00290896	intron-variant	RNF157	GRCh38.p7	17:76162017	CCTGGCCAAGGAGAA[A/G]GAAATGTAGCCAATG	114804
rs768428441	snp	C/G			upstream-variant-2KB	RNF157	GRCh38.p7	17:76241880	ACAGGCGTGAGCCAC[C/G]GCGCCCGGCACATTT	114804
rs768440333	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76207648	AGGAGTCGTTCTTGC[C/T]GCATGCTGCTGGATG	114804
rs768460920	in-del	-/T	1.65942e-05	0.00288042	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152518	GTGTTTTTCTCTGCG[-/T]TGCTGTCCTTAAAAT	114804
rs768491970	snp	A/G	1.64841e-05	0.00287085	missense, intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152393	AGCTTATTGTCCAGT[A/G]CTTTCACGCTTGCGA	114804
rs768565361	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76211241	AAATGTTTGCCAATT[C/T]AACAACTTGAATGCT	114804
rs768589736	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76226806	AGCTCATTTCGGTCA[C/T]GTTGCGGTGCTTTGC	114804
rs768595287	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76162726	AACCAAGGACTACCG[A/G]TTCATAATGAGAAAA	114804
rs768679280	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76239425	ATACCTCTGCCCTGT[C/G]CCAGAGCTGGTCCCA	114804
rs768707058	snp	A/G			upstream-variant-2KB	RNF157	GRCh38.p7	17:76241176	CCTTGTAGCCCTAAA[A/G]TTAGGAGAACATCGA	114804
rs768759496	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76198676	CTGTATCCGTTCTCA[C/T]GACTCTCTAATCTAC	114804
rs768813147	snp	C/T			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154024	TCTACTTCAGGTAAA[C/T]ATGGACCTGTATGTA	114804
rs768815481	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76166060	GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA	114804
rs768828523	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76177725	AAGGCCCAGGCTCAG[C/T]CAGAACAGAGCAGAG	114804
rs768837600	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76189063	GAACAAGGAAAAATT[A/G]AGAAACTAGCACACA	114804
rs768846101	in-del	-/CTCATGCGGTG			intron-variant	RNF157	GRCh38.p7	17:76186251	GACTCATGCCTGTAA[-/CTCATGCGGTG]TCCCAGCACTTTGGG	114804
rs768848787	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76182384	ATGAAATTGCCAGAC[C/T]ATGCCCAAATGCAGG	114804
rs768849386	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76204390	ACTCTGGTCCTCTCT[C/T]GTAGAACCTATCACA	114804
rs768874062	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76158992	GATGTTTAAGAGATA[C/T]GGATCACAAGGTTCC	114804
rs768905520	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76164897	GCCCTCCCTGATCTG[C/G]AGTTTCATTTTCCAT	114804
rs768962783	snp	C/T	9.89903e-05	0.00703458	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159365	TTGAGTTTGAGTCCC[C/T]GACTGCTGCTGTCAG	114804
rs768973533	snp	A/G			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147173	GTCTAAGTGTGGCAG[A/G]ATAAATATAAGGCAA	114804
rs769011366	snp	A/G			intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76154894	CACAGGTCTGTATAG[A/G]TCTATATGTGCCCTA	114804
rs769015834	snp	A/G	3.2981e-05	0.00406071	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159440	CCATCACTGCCATAT[A/G]AAGGGAGCATTCCTG	114804
rs769037051	snp	C/T	1.65655e-05	0.00287793	splice-acceptor-variant	RNF157	GRCh38.p7	17:76161649	CAGTGCCCGGAAGGC[C/T]GTGAAGGAGAAAACA	114804
rs769037752	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76176789	GCTTGCTCATGGAGC[A/G]CCAGGGCCAGGCCTG	114804
rs769090303	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76187935	TATTAATGTAAAGAT[A/G]TGCGGAAACCCTAAT	114804
rs769092399	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76206314	AGAGTTGGGCAGTAA[C/T]TATCCCAACAAAACA	114804
rs769100235	snp	C/T	1.67309e-05	0.00289226	intron-variant, downstream-variant-500B	RNF157	GRCh38.p7	17:76156181	GGTAAGGGGGAAGGA[C/T]ATGCAGCCACTCCCC	114804
rs769107218	snp	A/G	1.64806e-05	0.00287054	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	RNF157	GRCh38.p7	17:76212436	TTCAGGATGAGTTGA[A/G]TCAAACTTCTCTCCT	114804
rs769152355	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151490	GCTGAAGTGAGTCTT[C/T]GTTCAGGGAATGTTT	114804
rs769189637	in-del	-/AGG			intron-variant	RNF157	GRCh38.p7	17:76173808	TGTCAGAAACAAAGC[-/AGG]AGGAGAAGGTGGTGT	114804
rs769230211	snp	C/T	1.65168e-05	0.00287369	intron-variant	RNF157	GRCh38.p7	17:76212318	GTTACATTTTTTGAA[C/T]TGGCCACTTAAGCTC	114804
rs769242019	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76161745	TCCCAGCGCGCATCC[A/G]TTTGTCAGATCCAGC	114804
rs769275222	in-del	-/G			intron-variant	RNF157	GRCh38.p7	17:76188752	AGTGGGAAGTCAAAA[-/G]TTCAGCAAGAGGATT	114804
rs769323111	snp	A/G/T	0.000131801	0.00811693	missense, synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76161583	GATGATGGGGTTAAA[A/G/T]CTGGTTGGGGACAAG	114804
rs769324013	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76167382	ATACCACCATTTGTC[A/G]CTATACCAAGATGGC	114804
rs769354787	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76236414	AAAAGCAACCATCTC[C/T]GCAAAGCCATACCTT	114804
rs769354920	snp	C/T	1.66504e-05	0.0028853	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76164751	TCAAATACTTACTAC[C/T]TGTTTCTGTTTGAGG	114804
rs769403051	snp	C/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150892	TTGGCAGGGAGGACA[C/G]TGCTGGCACGGAGTG	114804
rs769404050	snp	G/T	1.65523e-05	0.00287678	stop-gained, nc-transcript-variant	RNF157	GRCh38.p7	17:76167123	GTTGTCTTTGGGAAT[G/T]TAGCTATTGATACAA	114804
rs769444512	snp	C/T	3.41501e-05	0.00413206	intron-variant	RNF157	GRCh38.p7	17:76164695	GAAGAAAGGAAAGAA[C/T]AAAAGGAAGGAAGGA	114804
rs769455259	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76192528	GAATACACGAACAAC[A/C]AGATCTTCGGAAGAG	114804
rs769480661	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76179656	TGAGCTCATGCCACT[A/G]CACTCCAGCCTGGGC	114804
rs769482338	in-del	-/T	1.6768e-05	0.00289546	intron-variant	RNF157	GRCh38.p7	17:76161804	TGTCCTCTTGTCCCC[-/T]CTCCCACCCACCAGT	114804
rs769506003	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76218256	TCAGACTTTTCAACA[C/G]AAACACTTTATGTCA	114804
rs769535632	in-del	-/A	3.3451e-05	0.00408954	intron-variant	RNF157	GRCh38.p7	17:76173828	GAAGGTGGTGTGTTT[-/A]AAAAGACCCACAGCT	114804
rs769540410	snp	C/T			utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142857	ACCACCTGAAGGCAA[C/T]AGGGAGAGCACAGGC	114804
rs769543385	snp	A/G	1.65061e-05	0.00287277	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76158439	GAGAGCTGTGTCTCC[A/G]ACTCGCTGCAGGAAT	114804
rs769565682	snp	A/G	1.65233e-05	0.00287426	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152473	CCTCTGGCCTGTAAC[A/G]GAGTTAATGCAGTTA	114804
rs769570168	in-del	-/ACTGT			intron-variant	RNF157	GRCh38.p7	17:76193635	AGGGAAATGGAAGAC[-/ACTGT]ACTGTCTAAGGTAAC	114804
rs769614156	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76184510	GCTTCGTATTTGCTT[C/G]AATGCTGTGAAGTGA	114804
rs769628847	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76158149	GAATATAAATGCTAC[-/A]AGGGCAGGGACTTTT	114804
rs769650586	in-del	-/TCTCGATCTC			intron-variant	RNF157	GRCh38.p7	17:76209976	CATTGGTCAGGATGG[-/TCTCGATCTC]TTGACCTTGTGATCC	114804
rs769704622	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76223781	AAACAAAAAACCAAA[C/G]AGACTGCACTGCCCA	114804
rs769720719	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76238370	AGACTTCTCTCATGT[A/G]TAACTTCTGATTTAA	114804
rs769772180	snp	C/G	3.29549e-05	0.00405911	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154270	GGAAGTAAAGGACCA[C/G]ATCTTTTACCACCTT	114804
rs769775671	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76155466	CCTGGCATTTTGGGG[G/T]CTTTGCAGCCATGCA	114804
rs769829355	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76218793	ACAAAAATTAGCCGG[A/G]AGTGATGGCATGTGT	114804
rs769847094	in-del	-/TGACTCAG			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151568	CCCGGAGGGGACATT[-/TGACTCAG]TCCGCTTGGGCAAGA	114804
rs769851691	in-del	-/C			intron-variant	RNF157	GRCh38.p7	17:76194838	GCTAACATGGTGAAA[-/C]CCCCGTCTCTACTAA	114804
rs769914628	snp	A/T	3.31813e-05	0.00407302	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167041	CGGAGGGATCCACGG[A/T]GTGGGAGGGCAGGCA	114804
rs769941288	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76176688	CTGGCCGGGTTACCC[A/T]CCAGCAGAGGAGCAG	114804
rs769948421	snp	C/G	1.64738e-05	0.00286995	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167696	GCCTGGTAATAGATG[C/G]TGATGGCTACCCGAG	114804
rs769959643	snp	A/G	1.64939e-05	0.0028717	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159476	TGGCCATCTCCAAGC[A/G]CGTGAAGTGGAGGAA	114804
rs769970150	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76188600	GCAACAGATAATTCC[C/T]CCCAAAGCAATGCAT	114804
rs769995492	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76195923	AGTTTACTATTGCCA[C/T]GGCAACACCTGGAAG	114804
rs770052299	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76176062	TTGTTCGTGGGCTGC[C/T]ACCCACCAAAGTTTG	114804
rs770103927	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76156752	AATTCCTGCCCAGCT[A/G]CTTTCTGATACAAAC	114804
rs770136991	snp	C/G	2.31532e-05	0.00340236	synonymous-codon, intron-variant, utr-variant-3-prime, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145238	AGAGGCTGGGGCTCA[C/G]ACAGCCAAAGGGCCC	114804
rs770142462	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76164696	AAGAAAGGAAAGAAT[A/C]AAAGGAAGGAAGGAC	114804
rs770165224	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76214592	ATTACTACACAGACT[A/G]TGGTGTAAAATAAGG	114804
rs770184306	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76187696	CATCCGGGGTTCAAG[C/T]GACTCTCCTGCCTCA	114804
rs770186707	snp	A/G	0.000214654	0.0103577	missense, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156258	TCCCTGTGCAAGACG[A/G]CTGGTCAATAGCTCC	114804
rs770189936	snp	A/G	9.90521e-05	0.00703678	missense, intron-variant, utr-variant-3-prime, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145309	ATGACAAGCGCCGGC[A/G]CTGGGCATTCCGACT	114804
rs770215731	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76181400	CTTAGAGAAGAGCTT[A/T]CTTGGAGCACAGTAT	114804
rs770221560	snp	C/T	1.65029e-05	0.00287248	missense, upstream-variant-2KB, nc-transcript-variant	RNF157	GRCh38.p7	17:76212456	ACTTCTCTCCTCCCA[C/T]AATGAAGTGGCTGGC	114804
rs770230522	in-del	-/C			intron-variant	RNF157	GRCh38.p7	17:76187852	ATCTGCCTGCCTTAG[-/C]CTTCCAAAATGCTGA	114804
rs770257916	snp	A/T	1.64844e-05	0.00287087	intron-variant	RNF157	GRCh38.p7	17:76166414	TGCCAGGAATATGCC[A/T]CAAAAGAGCAGTGTG	114804
rs770266445	snp	A/G	1.81069e-05	0.00300884	intron-variant	RNF157	GRCh38.p7	17:76164843	AGGGAGGGTAATAAA[A/G]CACCAGGTATTCTTC	114804
rs770268112	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76233926	TTTTAGTATATTGAC[C/T]GTGTTATACAACTAT	114804
rs770278370	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76190754	CTACTAAAAACACAA[A/G]AAATTAGCCGGGCAT	114804
rs770370170	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76205038	GTGATCCACCTGCCT[C/T]GGTGTCCCAAAGTGC	114804
rs770382216	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76231506	TCTCACCACGTTGAC[G/T]GGGCTGGTCTCAAAC	114804
rs770403523	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76206222	GGCAACAGGGCAAGA[C/T]CTTGTCTCAAAAGGA	114804
rs770424778	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76176441	TTTTTTTCTGCTCTT[-/A]AGAGTTGTCTCCCAT	114804
rs770532811	snp	A/G	3.30338e-05	0.00406397	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76161856	ACGCAGTCGGCAGAT[A/G]GGGCAGTTGTTGGCC	114804
rs770534214	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76159221	AAGCAGCTCTGGGAA[C/T]AGCCCAGAGGGTTAC	114804
rs770551775	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76239255	GGTCATGCAATTCAT[A/G]CTGGCCGGTGCTCAC	114804
rs770568009	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76178207	GTCGGGGAGCCCAGA[C/T]CTGGGAGCTGCCCAA	114804
rs770655629	snp	C/T	1.65157e-05	0.0028736	synonymous-codon, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156271	CGACTGGTCAATAGC[C/T]CCAGATGACGACAAG	114804
rs770686501	snp	A/C/G	6.59059e-05	0.00574014	missense, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154291	TTACCACCTTCCTGC[A/C/G]TGGGTGATCCATCCT	114804
rs770705505	snp	C/T	1.65614e-05	0.00287757	intron-variant	RNF157	GRCh38.p7	17:76167140	AGCTATTGATACAAG[C/T]GGGAGGCAAAGCAAA	114804
rs770720723	snp	A/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150795	AGGCCCTTGCCAATT[A/T]GGAATGGGAGCCTTG	114804
rs770724855	snp	A/G	5.07713e-05	0.00503816	intron-variant, utr-variant-3-prime, nc-transcript-variant	RNF157	GRCh38.p7	17:76156362	GGACATGGAGCAAGC[A/G]CCAGTCACCTGTGCT	114804
rs770758091	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76197212	GGGGAATAGGAGACA[C/T]GGGGCTGTATAATAT	114804
rs770846195	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76184009	AGCCTGGCCAGCATG[A/G]TGAAACCCCGTCTCT	114804
rs770860934	in-del	-/AGGTTCGCAGTCCTTGCCACCAGCC			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149234	GGACGGGAACCAACA[-/AGGTTCGCAGTCCTTGCCACCAGCC]AGGTCTCCTGGCAGA	114804
rs770880385	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76188517	AGCATTAACCACAAG[C/T]TTTCTGAGACTAAAA	114804
rs770908155	snp	A/G	3.36304e-05	0.0041005	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76155580	TCCTTCTTCTGAGGG[A/G]GCCCTGCTGGCAGGC	114804
rs770908466	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76171741	CCATTTTACAGATAA[A/G]AGAACCTGAAGCTCA	114804
rs770934670	snp	C/T	6.60458e-05	0.00574618	intron-variant	RNF157	GRCh38.p7	17:76167807	GCACATCTAGAAAAC[C/T]AGAGACTCAGCATTT	114804
rs770946469	in-del	-/ATA			intron-variant	RNF157	GRCh38.p7	17:76220336	TTAAGCTTCATCAGG[-/ATA]ATAAGGGCAAGGAAT	114804
rs770994316	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76174568	TGTTATTTGGGCAAT[C/G]AAAATGTTTTAACAT	114804
rs771021037	snp	C/T			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145683	GTTTTAAAGTTTGCC[C/T]ATATGTTACAATAGA	114804
rs771048097	snp	A/C	1.67363e-05	0.00289272	intron-variant	RNF157	GRCh38.p7	17:76161686	CAGGACATCCTGATA[A/C]AGGATTAAGAATGAA	114804
rs771066358	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76200269	AACAAAAACAAAAAC[A/C]AAAAAAAACCGAGGC	114804
rs771092768	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76187625	CTGAGACAGGTTCTC[A/T]CTCTGTCGCCCAGGC	114804
rs771110777	snp	C/T			intron-variant, nc-transcript-variant	RNF157	GRCh38.p7	17:76156496	TCACTTCAGCCCAAG[C/T]CTGGAATGACTGCCT	114804
rs771113620	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76207759	TGGAAGTCAGCTGTT[C/T]AGAACTCAAGCTACA	114804
rs771115054	snp	G/T	2.45697e-05	0.00350489	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76173720	ACGAGCCTCAGTGTG[G/T]CCTTTCGGATATTGA	114804
rs771163993	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76176246	ATTAAATATATGGAT[-/A]TTTTTTTGCCACAAA	114804
rs771182795	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76186405	CCAGCTACTCAGGAG[A/G]CTGAGGCAGGAGAAA	114804
rs771199748	snp	A/G	1.6631e-05	0.00288362	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76162583	TTGTACTTGTTTTCA[A/G]TTCCATAGATCTCCT	114804
rs771220005	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76184892	GGAAGTACACAAGAC[C/G]AACGTCATGGCTATA	114804
rs771222101	in-del	-/T			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152533	TTGCTGTCCTTAAAA[-/T]AAAAATCTTAAGGAT	114804
rs771228854	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76226465	AGTGTCATCCAACGT[A/G]GTCAAAAGGTCATCT	114804
rs771298181	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76233147	GGATGGTCTCGATCT[C/T]CTGACCTCATGACCC	114804
rs771325661	snp	C/T	1.65756e-05	0.00287881	intron-variant, missense	RNF157, RNF157-AS1	GRCh38.p7	17:76152325	GGGATCGTCTCCCAC[C/T]AAGTTCATGTTCAGC	114804
rs771336657	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76178948	AGAGATGAGATTTCC[A/G]AGGATTAAAGTGCTG	114804
rs771353600	snp	A/G	3.33483e-05	0.00408327	intron-variant	RNF157	GRCh38.p7	17:76159578	TTCTCTGAGGACTAG[A/G]GGAATCAGAGACAGG	114804
rs771387559	snp	C/T	3.30175e-05	0.00406296	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76166508	AGAGGGTAAACTTCT[C/T]GGTCTAAATCAAAGC	114804
rs771427258	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76202761	AGTCACAACAATGAT[A/C]ATCAGCCCTGGGGCC	114804
rs771427760	snp	G/T	3.30104e-05	0.00406252	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76159493	GTGAAGTGGAGGAAC[G/T]GCTGGGGACGGGGTG	114804
rs771444936	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76168115	CTTCTTCCCTTTCCT[C/T]GTCTTCAGAGGACAC	114804
rs771475014	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76167470	GAACCAGATCTCATC[C/T]GGCTGCAGAAAAAGA	114804
rs771478660	snp	C/T	4.98542e-05	0.00499245	intron-variant	RNF157	GRCh38.p7	17:76155331	CCCTGCAGAAGAGCA[C/T]AGTTTTTACAGGCTC	114804
rs771487347	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151437	AGCCACGTCGCTGAG[C/T]GAGTAAAGCACTGGA	114804
rs771520840	in-del	-/TTCA			intron-variant	RNF157	GRCh38.p7	17:76174381	AGGTTTATGGTTGTC[-/TTCA]TTCATCATTTACCAT	114804
rs771533292	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76182013	AGTACTGAACTAGGC[C/T]TGAGGGACACAGTGA	114804
rs771550886	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76226695	GCTTGGCCACCTCCA[C/T]GTAGTCATCTAAGAG	114804
rs771560759	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76200198	AGTGAGCCAAGATCG[C/T]GCCACTCCATGCCAG	114804
rs771634235	snp	C/T	3.2969e-05	0.00405998	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76240187	GTACACGGAATTAGA[C/T]GGGATGTCCACCTCC	114804
rs771650960	in-del	-/A			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153122	CCCTCTTTTTTTCTC[-/A]AGTGAAACAGAGAGA	114804
rs771669288	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76171586	TTTACCTGGAAATCC[C/G]AGAATCAGAATTTAT	114804
rs771677613	snp	C/T	3.30628e-05	0.00406575	intron-variant	RNF157	GRCh38.p7	17:76158365	CCTGGAGTACAACAC[C/T]CAAGAAGAGGAGAGG	114804
rs771708652	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76189222	GTGTTAATTTTCAGT[C/G]TGGATAAATGTGTTG	114804
rs771750523	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76204729	GGTCTATCTGTACTA[A/G]AGAAAGAAGAAAAGT	114804
rs771757340	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76170737	TGATTCTCAGCTTTT[A/C]TTTCTGCTAGTTCAG	114804
rs771760516	snp	C/T	3.306e-05	0.00406558	intron-variant, synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76155306	GCTGTCTGGAGACTC[C/T]GCTGGCAGCCCCTGC	114804
rs771763378	in-del	-/TAAA			intron-variant	RNF157	GRCh38.p7	17:76205724	GCAAGACTCCATCTC[-/TAAA]TAAATAAATAAATAA	114804
rs771779997	snp	A/C	4.95798e-05	0.0049787	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76166523	CGGTCTAAATCAAAG[A/C]CAAGCTGAAGGGAAA	114804
rs771784899	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76194289	TCTATCGTTTTGCTC[C/T]TTCCAGAATGACACA	114804
rs771802307	snp	C/T	1.65026e-05	0.00287246	synonymous-codon, intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152359	CTGACACTCACCAGG[C/T]AAGCAGACCTCAGAG	114804
rs771823821	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76162786	GCTTTTATTTACTTA[C/T]GTTTTCTCTTTGAGA	114804
rs771832481	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76195605	ATGTGTAATAGCCAA[A/G]ATGCCCCAAAAAAGC	114804
rs771855433	snp	C/T	1.65083e-05	0.00287296	missense, intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152460	GAAATGCGCACGTCC[C/T]CTGGCCTGTAACGGA	114804
rs771874489	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76208582	AACCTGTGGGGAAAA[G/T]AAAAAGAGAAACATG	114804
rs771886828	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76166125	GATTAGAGGTGCACA[A/C]TGCCATACCCAGCTG	114804
rs772021408	snp	C/T			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153792	ACCACGCCTTTAGTA[C/T]GTCTGCCGGCCCGAG	114804
rs772021813	snp	A/G	3.32231e-05	0.00407559	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76162602	CATAGATCTCCTGAA[A/G]GAGGTAGCTGACCCC	114804
rs772068686	snp	C/T			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145983	CAGCCCAGCAGACAC[C/T]AGCCCAAGAGCCTCG	114804
rs772093514	in-del	-/CA			intron-variant	RNF157	GRCh38.p7	17:76195163	GAAACATATTCATGT[-/CA]CAGAACTCCAGACAG	114804
rs772103742	snp	A/G			intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76154968	AGTGGAATGAAGGAC[A/G]ATATATTCTCAAGGC	114804
rs772117103	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76229578	TTCAATCACCTGCCA[C/T]ATCTTTTCATCCAGA	114804
rs772127322	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76160183	CCTTCTCATAGATCC[C/T]CTAAGTTTTCTAACT	114804
rs772165406	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76155555	CGGTTCCCGTCCCTT[C/T]CCTTACCTCTCCTTC	114804
rs772179370	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76186115	AATCTTCCCTACTCT[C/T]TATTTCAAAAATAAA	114804
rs772189075	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76215980	AGGGGAGGTACCTAG[C/T]TGCCTTAAGTAGAAG	114804
rs772213100	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76199804	ATAGAAATCCAACTC[C/T]ATAAAACAGAGGGAT	114804
rs772216956	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76176721	TGGCAGAAGAGCAGC[A/G]CGGTAGGGCAAAGAG	114804
rs772243431	snp	A/G	2.28658e-05	0.00338118	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145190	GCTGAGTGAGGATGG[A/G]TGGAATGCAGGGCAG	114804
rs772271752	snp	C/T	1.67809e-05	0.00289658	intron-variant	RNF157	GRCh38.p7	17:76164723	GGACCCTAATACTAA[C/T]AGTCTGTGGTCTTCA	114804
rs772300928	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76198703	CTACCTTCTACACTT[C/T]ATCTGAGAGATCTTT	114804
rs772330683	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76237892	GTTCAAGACTTGCCT[A/G]GCCAATATGGTGAAA	114804
rs772332857	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76173475	ATTTCTAGGCAAGCG[A/G]AAGTTTTTCACAAAC	114804
rs772348498	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76233011	CTGCAACCTCTGCCT[C/G]CTGGGTTCAAGTGAT	114804
rs772356017	snp	A/G			intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145500	CGAGCCACAGCACTC[A/G]TGTGTGAGAACGGAG	114804
rs772380066	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76178134	TAACACAAACAGGAC[C/T]GAAACATGCTCCTTG	114804
rs772389934	in-del	-/TTTA			intron-variant	RNF157	GRCh38.p7	17:76157734	AAGGGCAGGGACCAC[-/TTTA]TTTACCTTCCTGTGC	114804
rs772398605	snp	C/T	1.66371e-05	0.00288414	intron-variant	RNF157	GRCh38.p7	17:76158532	GGAAAAGCAGCTATA[C/T]CCAACGTCCATTTAA	114804
rs772405112	snp	A/G	1.67116e-05	0.0028906	intron-variant	RNF157	GRCh38.p7	17:76159585	AGGACTAGGGGAATC[A/G]GAGACAGGTTGAAAA	114804
rs772494025	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76224577	TATAATGCTACAGTG[A/C]TGCTTTTGTTCTTCA	114804
rs772517467	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76225626	TCTGTATTTATGGCA[C/T]GACCTCATTGTTTTT	114804
rs772524732	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76230960	TTTTCTTTTTTAAAG[C/T]TAGGGTCTCACTCTA	114804
rs772527541	snp	A/G	1.64754e-05	0.00287009	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161536	CGAGCCCAACTTACT[A/G]GATGCTCTTCAGAGT	114804
rs772557524	snp	A/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149650	GACACATTCTGCCTA[A/G]AGAGACGTGCTTTTC	114804
rs772594167	snp	A/C	3.35892e-05	0.00409798	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155583	TTCTTCTGAGGGGGC[A/C]CTGCTGGCAGGCTGG	114804
rs772601518	snp	C/T	5.03918e-05	0.0050193	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155696	TCTGGGAGGATGCCA[C/T]GGACATGACAGACTG	114804
rs772628792	in-del	-/TTTCT			intron-variant	RNF157	GRCh38.p7	17:76204782	TTCTTTCTTTCTTTC[-/TTTCT]TTTTTTTTTTTTTTG	114804
rs772676828	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76201065	ATTTTCCTACTTCTA[A/G]ATATTCTTCTAAACC	114804
rs772686608	in-del	-/C			intron-variant	RNF157	GRCh38.p7	17:76175478	CAGTGCATCAGGAGG[-/C]CTTGACATGGTAAAA	114804
rs772696079	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76203139	GGGATTACAGGCATG[C/T]ACCACCATGCCTGGC	114804
rs772714860	snp	C/G			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147784	AGGTGCCGCCATTTT[C/G]TCTGGCTGAATCCAG	114804
rs772746027	in-del	-/C	1.68434e-05	0.00290197	intron-variant	RNF157	GRCh38.p7	17:76155550	CAGGGCGGTTCCCGT[-/C]CCTTCCCTTACCTCT	114804
rs772773259	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76236556	GCTCTAAATTGCTTT[C/T]TATGCTAATGTAGAA	114804
rs772781797	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76159123	AAAAAAGAATACATA[A/G]GAGATTTGTCTCATC	114804
rs772801011	in-del	-/AGAGTACATTC	1.82947e-05	0.00302441	intron-variant	RNF157	GRCh38.p7	17:76162520	CTTGGCCTCCTGGAA[-/AGAGTACATTC]AGAATTTTGGGTAAA	114804
rs772804725	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76171637	AAAACAAAGAACACC[C/T]TTCAAGTTAACATTT	114804
rs772826312	snp	C/T			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153799	CTTTAGTACGTCTGC[C/T]GGCCCGAGAGTCCTC	114804
rs772859956	in-del	-/ATTT			intron-variant	RNF157	GRCh38.p7	17:76234299	CATCGGTTGATGAAC[-/ATTT]GGGTTATTTCCACAT	114804
rs772891246	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76189237	CTGGATAAATGTGTT[A/G]CAGTTATGTAAGATG	114804
rs772908082	in-del	-/CACA			intron-variant	RNF157	GRCh38.p7	17:76202129	TCTCTCTCTCTCTCT[-/CACA]CACACACACACACAC	114804
rs772936542	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76204397	TCCTCTCTCGTAGAA[C/T]CTATCACAGTCCCTC	114804
rs772955106	snp	C/G	2.31742e-05	0.0034039	missense, intron-variant, utr-variant-3-prime, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145240	AGGCTGGGGCTCAGA[C/G]AGCCAAAGGGCCCCA	114804
rs772958542	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76202005	CACAGCTCAAAATTT[A/C]ATCAATATTTCCAGG	114804
rs773002481	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76195626	CCAAAAAAGCTCAAT[A/G]CCTGCAAACAATAGA	114804
rs773019051	snp	A/G	6.6107e-05	0.00574884	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152476	CTGGCCTGTAACGGA[A/G]TTAATGCAGTTAGAG	114804
rs773030405	in-del	-/AAAT			intron-variant	RNF157	GRCh38.p7	17:76186944	ACTCCGACTCAAAAT[-/AAAT]AAATAAATAAATAAA	114804
rs773065354	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76180008	AGACCAGATAAAGTC[C/T]TTCTGATGTAAGCAT	114804
rs773072026	snp	A/C	1.6477e-05	0.00287024	missense, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154287	TCTTTTACCACCTTC[A/C]TGCGTGGGTGATCCA	114804
rs773083131	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76181055	GACTCAAAAGATTCA[C/T]GTAATCATCCAGGGT	114804
rs773122679	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76215701	TATTAAATAAAACAA[C/T]GTGGATAAAATCACT	114804
rs773134181	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76166792	TCCTAGGCTAATGGG[A/C]TATTTCCATTCCTAG	114804
rs773169203	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76184786	CCTTGCACACAAAAA[C/T]GCTTTGTCTTCAGAT	114804
rs773195418	snp	G/T			upstream-variant-2KB	RNF157	GRCh38.p7	17:76242198	CCTTGTAACTGCTGG[G/T]TAAAGGTAAAATGCA	114804
rs773199842	snp	A/C			splice-donor-variant	RNF157	GRCh38.p7	17:76155561	CCGTCCCTTCCCTTA[A/C]CTCTCCTTCTTCTGA	114804
rs773236198	in-del	-/TA			intron-variant	RNF157	GRCh38.p7	17:76221936	GGTCACATACTGTAG[-/TA]TGATTCCATGTATAT	114804
rs773340251	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76231949	TCTGCTTTCTATCTC[C/T]ATAAATGTGCTTCTT	114804
rs773342205	snp	A/C	1.64781e-05	0.00287033	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167706	AGATGGTGATGGCTA[A/C]CCGAGCATCTGTGTC	114804
rs773363609	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76173487	GCGAAAGTTTTTCAC[A/T]AACACAGACGATTGC	114804
rs773387468	snp	C/T	1.64836e-05	0.0028708	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167784	CTCCAGGGCTCTTCA[C/T]TTCCTCAGCACATCT	114804
rs773389453	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76160750	TGCTAAACTTTTTAG[A/G]TGGTAAAATGTATGG	114804
rs773393669	snp	C/T	3.29679e-05	0.00405991	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76161883	GGCCTGGTAGCGCAG[C/T]GTGTCTGCACAGGTG	114804
rs773417554	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76206733	TCGGCTCACTGCAAT[C/T]GGCTCACTCCAGCCT	114804
rs773421670	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76238568	GTTTACCTATGTTAA[A/G]TCCCACATATGAAAG	114804
rs773448797	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76219091	ACTTCAAATGCTGGA[A/G]TAAAGAGGAGAGGTG	114804
rs773454260	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76174496	AGCCAAAAATTTCAC[C/T]GGGAATTGCCTTCTG	114804
rs773455518	snp	A/G	1.65869e-05	0.00287979	intron-variant	RNF157	GRCh38.p7	17:76155327	CAGCCCCTGCAGAAG[A/G]GCACAGTTTTTACAG	114804
rs773464039	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76165077	AATTAAACTTTATCA[C/T]AGGTGTGGATGTAGT	114804
rs773468219	snp	A/G	1.95276e-05	0.00312465	stop-gained, intron-variant, utr-variant-3-prime, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145312	ACAAGCGCCGGCGCT[A/G]GGCATTCCGACTGAC	114804
rs773553903	in-del	-/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76148948	GACTTTCCTGCCACC[-/T]TATGTAACAGTCTGC	114804
rs773581352	in-del	-/AAT			intron-variant	RNF157	GRCh38.p7	17:76162873	AAATTTCACAAATAC[-/AAT]AATAATACTTGCACT	114804
rs773610884	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76194915	AGCTACTCAGGAGGC[A/T]GAGGCAGCAGAATGG	114804
rs773713468	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76234802	AATTTCTCCCATTCT[C/T]TGAGTTCTCTCTTTT	114804
rs773816805	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76198712	ACACTTCATCTGAGA[A/G]ATCTTTTAAAATGTG	114804
rs773826600	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76204941	AAGCACCTGCCACCA[C/T]GCCCAGCTAATTTTT	114804
rs773836548	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76166430	CAAAAGAGCAGTGTG[C/T]ACAGCCAAAGAGGAC	114804
rs773847894	snp	A/C	1.64923e-05	0.00287156	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159390	TGTCAGACAGGCGGT[A/C]AAGAGGCGAGATCGT	114804
rs773906899	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76211486	CACCAAACTTGCAGA[A/C]TATTTCAAGGCAGTG	114804
rs773908054	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76214939	TGATTAAACGAATGC[C/T]GCTTACCTCTAATTT	114804
rs773910643	snp	A/G	1.68525e-05	0.00290275	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212490	ATAGCTTCCTAGAGA[A/G]GAACAAACAAAAAAA	114804
rs773917769	snp	C/T	1.65438e-05	0.00287605	intron-variant, missense	RNF157, RNF157-AS1	GRCh38.p7	17:76152340	CAAGTTCATGTTCAG[C/T]AGACTGACACTCACC	114804
rs773951771	snp	C/T	1.6504e-05	0.00287258	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161863	CGGCAGATGGGGCAG[C/T]TGTTGGCCTGGTAGC	114804
rs773955465	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76187939	AATGTAAAGATGTGC[A/G]GAAACCCTAATGGAA	114804
rs773959869	snp	C/T	3.29794e-05	0.00406061	intron-variant	RNF157	GRCh38.p7	17:76165479	CTAAAGGCAATAAAG[C/T]GAGGCCCTCTAAAGT	114804
rs773963583	snp	G/T	7.01705e-05	0.00592287	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76240178	CGGGTAGCGGTACAC[G/T]GAATTAGACGGGATG	114804
rs773975058	snp	A/G	1.65658e-05	0.00287795	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76167053	CGGTGTGGGAGGGCA[A/G]GCAGAACTGCTGACA	114804
rs774004698	snp	G/T			synonymous-codon, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156277	GTCAATAGCTCCAGA[G/T]GACGACAAGGTGAGA	114804
rs774010884	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76180964	ACAGTCCAACATGCC[A/G]GAGAAATACAGTAGC	114804
rs774034204	in-del	-/AAA			intron-variant	RNF157	GRCh38.p7	17:76220386	TTCGTAATGATATCT[-/AAA]AAAAAAAAAAAAAAA	114804
rs774043015	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76201975	AGAGGTGAAACAGTT[A/G]GGCCAAAGGGTACGC	114804
rs774069608	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151649	CACTAACTAAAAAGG[C/T]ACTCGGTGCTTAAAG	114804
rs774099632	snp	A/G			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213315	TGGCTCATGCCTGTA[A/G]TCCCAGCACTTTGGG	114804
rs774124412	snp	C/T	1.64784e-05	0.00287035	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76167665	CCTGGCAATACCATT[C/T]TGGAACTCTTCCGTG	114804
rs774195771	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76194073	TTTGTTGGTTTGTTT[A/G]TCAAGGTATAATTTA	114804
rs774209506	snp	A/C/G	3.31259e-05	0.00406965	intron-variant	RNF157	GRCh38.p7	17:76167143	TATTGATACAAGTGG[A/C/G]AGGCAAAGCAAAAGT	114804
rs774212937	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76170295	TGCAGTGCTGTGATC[A/G]TGACTCATTGCAGCC	114804
rs774258221	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76191673	CAGCTCCTAGGAAGG[C/T]TGACGTGGGAGGACT	114804
rs774263445	snp	A/G			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152639	TCACGTTGTGTGGGC[A/G]TGTCTGTGTTCTCGC	114804
rs774264765	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76239438	GTCCCAGAGCTGGTC[C/T]CACTCCAAAACCCAG	114804
rs774288685	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76227905	AAAAAAGAGGTAGTG[A/T]CAGGTCCCCAAATCT	114804
rs774314513	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76166252	ACTGCTGGGATTATA[C/T]GTGTGAGCCACTGTG	114804
rs774389581	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76179765	AACAGGTAAGTATGA[A/G]AGGAAAGAAAACTAA	114804
rs774430994	snp	A/G	1.66172e-05	0.00288242	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76162588	CTTGTTTTCAATTCC[A/G]TAGATCTCCTGAAGG	114804
rs774447918	snp	A/T	1.65378e-05	0.00287552	intron-variant	RNF157	GRCh38.p7	17:76167816	GAAAACCAGAGACTC[A/T]GCATTTGCAGAGTAG	114804
rs774460614	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76173221	AACCCTGGAGATGGA[A/G]CGTGCAGTGAGCCGA	114804
rs774460686	snp	A/G			upstream-variant-2KB	RNF157	GRCh38.p7	17:76241888	GAGCCACCGCGCCCG[A/G]CACATTTCGTATTTT	114804
rs774475453	snp	C/G	1.65392e-05	0.00287564	synonymous-codon, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156217	TTATGTACCTTCTGG[C/G]GAGGAAATAGTGGAT	114804
rs774498778	snp	C/G	3.41274e-05	0.00413068	intron-variant	RNF157	GRCh38.p7	17:76162033	GAAATGTAGCCAATG[C/G]CACAAAGCCCTTCCT	114804
rs774503589	snp	A/C			intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76154938	ACCTGTGACACAGTC[A/C]TCCATGTAAATACTA	114804
rs774551940	snp	A/G			utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76143113	GCCAAGAGAAGGCAG[A/G]GGGAGGGAGGAAGAG	114804
rs774582888	snp	A/C/G	3.30231e-05	0.00406333	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159498	GTGGAGGAACTGCTG[A/C/G]GGACGGGGTGAGGGG	114804
rs774590692	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76184680	TCACCAGCTTAGAAT[A/G]AATGGTAATCACAAA	114804
rs774602442	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76182409	TGCAGGCCAGAAGGG[C/T]GCACGTGCATTCACA	114804
rs774649415	snp	A/G	3.29674e-05	0.00405988	intron-variant	RNF157	GRCh38.p7	17:76166431	AAAAGAGCAGTGTGC[A/G]CAGCCAAAGAGGACA	114804
rs774678367	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76198681	TCCGTTCTCATGACT[C/T]TCTAATCTACCTTCT	114804
rs774683092	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76194908	TAGTCCCAGCTACTC[-/A]GGAGGCTGAGGCAGC	114804
rs774723666	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149529	AGACGCCTATTTATT[C/T]CACGGGACCTACCAA	114804
rs774748026	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76236500	ATGTATGACTTCTAA[C/T]TCAAAAATTACAAAA	114804
rs774795668	snp	A/G	3.27102e-05	0.00404401	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76240189	ACACGGAATTAGACG[A/G]GATGTCCACCTCCTC	114804
rs774826795	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76222570	ATCGTAAGCAAGATA[C/G]AGAACTTTACCAAAA	114804
rs774833158	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76224969	TTGAGGTCAGGAGTT[C/T]GAGACCAACCTGGCC	114804
rs774885645	in-del	-/AACT			intron-variant	RNF157	GRCh38.p7	17:76163916	GTGATTATATTGGAA[-/AACT]AATTTATCCTAAGAT	114804
rs774932725	snp	C/G	0.000160644	0.00896083	missense, intron-variant, utr-variant-3-prime, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145260	AAAGGGCCCCACACA[C/G]AGGGCCTCGTCTCAG	114804
rs774958836	snp	A/G	1.68035e-05	0.00289853	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155581	CCTTCTTCTGAGGGG[A/G]CCCTGCTGGCAGGCT	114804
rs774976521	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76226747	CAAACCCGACTGGTC[A/G]AAGGGGGACATCAAG	114804
rs774979009	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76176810	GCCAGGCCTGGGCGC[A/G]GAGCTGGGGCCATGC	114804
rs775020980	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76224501	AACAATAAGCTTTAG[A/G]TCACAAAAATAAGAA	114804
rs775091741	snp	A/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151491	CTGAAGTGAGTCTTC[A/G]TTCAGGGAATGTTTA	114804
rs775145061	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76218813	ATGGCATGTGTCTGT[A/T]GTCCCAGCTACTCGG	114804
rs775170745	snp	C/T			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212974	AAATAAGTAAAATCA[C/T]AGCAGGGAAAACCCC	114804
rs775179415	snp	C/G	1.65293e-05	0.00287479	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76166524	GGTCTAAATCAAAGC[C/G]AAGCTGAAGGGAAAG	114804
rs775227822	snp	A/G	4.94222e-05	0.00497078	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167688	CTTCCGTGGCCTGGT[A/G]ATAGATGGTGATGGC	114804
rs775264363	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150912	GGCACGGAGTGAACA[C/T]GAACTTTCATACCAA	114804
rs775319363	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76238477	CAAAAGTTTTGGTTT[A/G]GTCTATTGTCTTTTT	114804
rs775369960	snp	A/T	1.64887e-05	0.00287125	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161875	CAGTTGTTGGCCTGG[A/T]AGCGCAGCGTGTCTG	114804
rs775381517	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76161826	CCCACCAGTCCCCCT[G/T]CCGCTCTGGGGCTTA	114804
rs775409664	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76205108	CTTCCTCCCTCCCTC[A/G]TTCCCTCCCTTCCTC	114804
rs775413519	snp	C/G			upstream-variant-2KB	RNF157	GRCh38.p7	17:76242303	CGGCTCTGTTCAGAA[C/G]CCTTGGTTCTTCCTG	114804
rs775415451	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76208835	AAAAATTAGCCAGGT[A/G]TGGTGGCAGGCACCT	114804
rs775448124	snp	C/T	1.67332e-05	0.00289246	intron-variant	RNF157	GRCh38.p7	17:76164728	CTAATACTAACAGTC[C/T]GTGGTCTTCAAATAC	114804
rs775478178	in-del	-/CCA	2.32102e-05	0.00340655	cds-indel, intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145243	CTGGGGCTCAGACAG[-/CCA]AAGGGCCCCACACAC	114804
rs775532377	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76192756	TGAAAGACTGGAAAA[C/T]GAAGATGAAATGATT	114804
rs775600925	snp	C/T	4.98351e-05	0.0049915	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76162607	ATCTCCTGAAGGAGG[C/T]AGCTGACCCCGTCTA	114804
rs775604197	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76191081	ATAAACCTCTTGTGT[C/T]ACCAGCATTTAAGTT	114804
rs775620298	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76206487	CTTCAGAAGCCCAGT[C/T]TACTACTTAAGACAG	114804
rs775640157	snp	C/T			intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153157	AACAAATCCATTCCA[C/T]GGGCTAGGGAATGTC	114804
rs775653428	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76181374	TCTTTAACAGGAGTA[C/T]CTAAGGTCTTCTTAG	114804
rs775654320	snp	G/T	1.65094e-05	0.00287305	stop-gained, nc-transcript-variant	RNF157	GRCh38.p7	17:76158447	TGTCTCCGACTCGCT[G/T]CAGGAATGCTCATCT	114804
rs775721482	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76229786	TGCTTCTGTTGCTCC[C/T]TGATGGAACCTAAAC	114804
rs775722732	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76176712	GGAGCAGCGTGGCAG[A/G]AGAGCAGCGCGGTAG	114804
rs775727131	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76195962	CTCTTTCATGGCAAT[A/G]ACCCAATGACCCGGA	114804
rs775758458	snp	C/G			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153889	GTCCTCCCCCTCCCC[C/G]CAGTGGAAGAAATGG	114804
rs775784320	snp	A/C	3.35014e-05	0.00409262	intron-variant	RNF157	GRCh38.p7	17:76159590	TAGGGGAATCAGAGA[A/C]AGGTTGAAAAATTAA	114804
rs775793730	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76222451	ATAATTTTATGTTAC[A/G]TGAACTTCGCCTCAA	114804
rs775841441	snp	C/T	1.6786e-05	0.00289702	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155588	CTGAGGGGGCCCTGC[C/T]GGCAGGCTGGGGGGA	114804
rs775841509	snp	A/G	1.64751e-05	0.00287007	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161537	GAGCCCAACTTACTG[A/G]ATGCTCTTCAGAGTC	114804
rs775873473	in-del	-/GCACGTGAGTGAAGAAGCCCAAACA	1.64914e-05	0.00287149	intron-variant	RNF157	GRCh38.p7	17:76165561	CTGAAAGAAACAAAG[-/GCACGTGAGTGAAGAAGCCCAAACA]GCACATCTTGATGCC	114804
rs775901671	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76200889	GGCACCAAGAGGACC[A/G]AGCTCCCTGACTCTC	114804
rs775913687	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76201881	TCTAATTTTGCACTA[C/T]TACAAGTAATGCTAC	114804
rs775918590	snp	A/G	1.67981e-05	0.00289806	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76164793	GAAAGTTCCATCTGT[A/G]TGCTGGAATGAAAAT	114804
rs775960311	snp	A/G			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147089	GGATCTTTACTCCCT[A/G]GGGGTGGGTACTGGA	114804
rs775963637	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76233927	TTTAGTATATTGACC[A/G]TGTTATACAACTATT	114804
rs775967205	snp	A/G	3.36298e-05	0.00410046	intron-variant	RNF157	GRCh38.p7	17:76166556	AAAGGAAAGGAAAAA[A/G]AAAGAGGACTTAACA	114804
rs776022415	snp	C/T	0.000117886	0.00767652	intron-variant	RNF157	GRCh38.p7	17:76159612	AAAAATTAATTAGGT[C/T]CTTTTTGTTTTATGA	114804
rs776065269	snp	C/G			intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76154872	GGGGTAGGCAGAAAC[C/G]TCACCACACAGGTCT	114804
rs776083347	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76221029	AGGAGGCTGAGGCGG[C/G]AGAATTACTTGAACT	114804
rs776096534	in-del	-/GCCTTTTCTAG			intron-variant	RNF157	GRCh38.p7	17:76177638	GTGGGAACTTGTGTT[-/GCCTTTTCTAG]GCCTGCCCATGGATG	114804
rs776109025	snp	C/G	2.27182e-05	0.00337025	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76173741	CGGATATTGACCAGG[C/G]TTCTCAGAGTCTTCA	114804
rs776157298	in-del	-/A	8.23839e-05	0.00641757	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154261	ATAACTAAAGGAAGT[-/A]AAGGACCAGATCTTT	114804
rs776157962	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76176756	CCCGAGGCGGAGCTG[A/G]GCCTTGGCCAGTGTC	114804
rs776213813	snp	A/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150830	CAGCCCCACGCGAGC[A/G]CCTCCCAGGTGTGTG	114804
rs776222227	snp	C/T	1.66109e-05	0.00288187	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167034	GCCCACTCGGAGGGA[C/T]CCACGGTGTGGGAGG	114804
rs776239065	snp	C/T	1.6489e-05	0.00287128	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76166479	CTCCTTCATCCACCA[C/T]GGCATGTACCACTAG	114804
rs776286064	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76225849	CTGCCCTCTCTTTTA[A/G]AGCCTCGTTCTTCTT	114804
rs776301777	snp	A/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149850	ACCACCCTGACCAAC[A/G]TGGTAAAACTCCGTC	114804
rs776344451	snp	C/G	3.29484e-05	0.00405871	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161571	TGTCTGGGATGAGAT[C/G]ATGGGGTTAAAGCTG	114804
rs776358352	snp	A/G	0.000272572	0.011671	intron-variant	RNF157	GRCh38.p7	17:76162018	CTGGCCAAGGAGAAA[A/G]AAATGTAGCCAATGG	114804
rs776368623	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76168926	TTCACCTCCCAGCGT[C/T]GCTCCCAAGAAGTCT	114804
rs776412377	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76159257	CCTAAGTCCCCAGGA[C/T]GTGGGCCAGCACCAA	114804
rs776418539	snp	A/G	1.65048e-05	0.00287265	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76158433	CTCTGAGAGAGCTGT[A/G]TCTCCGACTCGCTGC	114804
rs776473222	in-del	-/G	1.64741e-05	0.00286998	frameshift-variant, nc-transcript-variant	RNF157	GRCh38.p7	17:76161566	TCAGATGTCTGGGAT[-/G]AGATGATGGGGTTAA	114804
rs776487631	snp	A/G	1.6522e-05	0.00287414	intron-variant	RNF157	GRCh38.p7	17:76158380	CCAAGAAGAGGAGAG[A/G]AATGTCAATTACCTC	114804
rs776501758	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76170910	ATTTATTTATTTTAT[C/T]GAGATGGAGTCTCAC	114804
rs776503183	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76171777	TCATTCAAGCAAGCA[C/T]CTGTGGACCTGGGAG	114804
rs776551929	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76238162	ACGGTTCCTTTCAGG[A/G]CTAATACTGTAATCC	114804
rs776605863	snp	C/T			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145778	GAGAAGACTGTTCGT[C/T]CTGGCCGAGTGTTAA	114804
rs776657582	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76182356	TCGGCAAAGCGCCAC[C/G]TGGTGACGAAAGATG	114804
rs776670305	in-del	-/GACT			upstream-variant-2KB	RNF157	GRCh38.p7	17:76241460	TTTCCTGAGAGAGTG[-/GACT]GACTGATCAGCAAAC	114804
rs776674896	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76192206	ACTGAATACCACAGC[A/G]GTTCTTTGTACTCTG	114804
rs776696253	snp	C/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151731	ATGAGGAGGAATAAG[C/G]GGCACTCTGACAACC	114804
rs776704365	snp	C/T	1.6516e-05	0.00287362	intron-variant	RNF157	GRCh38.p7	17:76155229	TGTGGGAAGGGGGCA[C/T]CACTCCGTGCTGTTG	114804
rs776754263	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76222243	CCCAGCTACTTGGGA[A/G]GCTGAGGCACAAGAA	114804
rs776757804	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76202844	CATGTTTATTTGCAA[C/T]GCTGTTAATCCTATT	114804
rs776778778	snp	C/G	1.6476e-05	0.00287014	missense, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154311	TGATCCATCCTCTTC[C/G]TCTATAACATCATTT	114804
rs776785767	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76162107	ATAAGTAATAATTAC[A/G]AACAAAATCTGCATT	114804
rs776813864	snp	A/G	1.65696e-05	0.00287828	intron-variant	RNF157	GRCh38.p7	17:76167154	GTGGGAGGCAAAGCA[A/G]AAGTCAGTATCCGGC	114804
rs776843885	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76198753	GCCCCAGTTTAAAGC[C/T]CATTAGTGGTTCCCC	114804
rs776858549	snp	C/T	1.64914e-05	0.00287149	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159386	CTGCTGTCAGACAGG[C/T]GGTCAAGAGGCGAGA	114804
rs776866869	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76174578	GCAATCAAAATGTTT[C/T]AACATATAATTCCCA	114804
rs776873218	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76194331	AATGCTTAAGTAAAA[C/T]AGCCAAAGGCCTCAT	114804
rs776885996	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76207898	GAAGAGGCGCTCCAA[C/G]AGAACATATCACTGC	114804
rs776915085	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76179538	TCTGTACTAAAAATA[C/T]AAAAATTAGCTGGGT	114804
rs776916706	snp	C/T	0.000117146	0.0076524	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76155622	GAGAGCCTCTCCCTC[C/T]TCTTCAGTGCCAGGG	114804
rs776921225	snp	C/T	9.90851e-05	0.00703795	intron-variant	RNF157	GRCh38.p7	17:76212319	TTACATTTTTTGAAT[C/T]GGCCACTTAAGCTCC	114804
rs776995475	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76239689	GAGACGGCAGCGCAG[A/G]GATAGCACCTGGCGC	114804
rs777004876	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76167231	TCAACAGGGTCTAGC[A/G]AAGAGAAGAAAGGGT	114804
rs777008889	snp	A/G	1.6693e-05	0.00288898	intron-variant, downstream-variant-500B	RNF157	GRCh38.p7	17:76156187	GGGGAAGGACATGCA[A/G]CCACTCCCCGCTCCT	114804
rs777020531	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76176931	CAGGTTCCTGTGCCT[C/T]GGGAGGAGGTTCTGC	114804
rs777036807	snp	C/T			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212839	ACACTCCAGTCTGGG[C/T]GACAGAGTGAGACTC	114804
rs777038055	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76219054	TGACAAACTTTAGGT[A/G]TAAGTGAGAGTCAAA	114804
rs777083177	in-del	-/AAAGAAAG			intron-variant	RNF157	GRCh38.p7	17:76210601	CCAAAAAAAAAAAAA[-/AAAGAAAG]AAAGAAAGAAAGAAA	114804
rs777098787	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76156592	CAAAGACTGCAGCTC[A/G]GGTGACACAGGTCAC	114804
rs777108561	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76176272	ACAAAAGGCAAAAAT[-/A]AAGGAAGTGATCATT	114804
rs777172995	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76183910	ATAGCAAAGTACAGG[C/T]TGGGAGCGGTGGCTC	114804
rs777182089	snp	A/G			utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76144847	TGGTTATGATGTGCC[A/G]GAGACCAGGAAATGC	114804
rs777191811	snp	A/G			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146811	GAGGACCTGTTCAGC[A/G]GACAAGGCCGACCAA	114804
rs777230915	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76233180	CTGCCTCAGCCTCCC[A/G]AAGTGCTGGGATTAC	114804
rs777250877	snp	C/T	1.66396e-05	0.00288436	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76164757	ACTTACTACTTGTTT[C/T]TGTTTGAGGGGCTTG	114804
rs777291061	snp	C/T	8.24994e-05	0.00642206	intron-variant, missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155269	CTGCATCCTGCTCTC[C/T]AGCTGGGAGGCCAGC	114804
rs777304969	snp	A/G			utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142575	CCACAAGTGTACTCC[A/G]GGGAGAGGGGTACAC	114804
rs777326304	snp	A/G	1.65141e-05	0.00287346	missense, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156266	CAAGACGACTGGTCA[A/G]TAGCTCCAGATGACG	114804
rs777328572	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76184978	GTTAAGCAATTCTCT[C/T]TGTTCACCTTAACAG	114804
rs777329811	in-del	-/TCT			intron-variant	RNF157	GRCh38.p7	17:76184332	TGGTACTACATAATC[-/TCT]TTTTTTATAGGGTTT	114804
rs777377975	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76191278	CCCAGGAGTTCAAGA[C/T]CGGTTAGGGCAACAT	114804
rs777405833	in-del	-/A	8.58804e-05	0.00655231	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212498	TAGAGAGGAACAAAC[-/A]AAAAAAAATCAAACA	114804
rs777406713	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76232209	GCAACGTAGTGGGAC[C/G]CCGTCTTTACAAAAC	114804
rs777425272	snp	C/T	1.65086e-05	0.00287298	intron-variant	RNF157	GRCh38.p7	17:76167630	GGGAAGGAAGTGGCT[C/T]TCCTGGTCTCCTGAT	114804
rs777436266	snp	A/G	1.69115e-05	0.00290782	intron-variant	RNF157	GRCh38.p7	17:76164801	CATCTGTGTGCTGGA[A/G]TGAAAATATGAAAGT	114804
rs777462691	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76164554	CAGGCCACCCAAGTC[A/G]TTTGTAATAGCTTGT	114804
rs777471337	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76173869	TTACAGTTTGCCAAG[A/T]ATAGCCCTAAGAGGT	114804
rs777481888	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76234124	TCTTATAAATGAGAT[C/T]ATTCAATAGATGGCC	114804
rs777553576	snp	C/T	1.64749e-05	0.00287005	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167759	TGGACTTTAGCTTTA[C/T]TGGCCTCTTCTCCAG	114804
rs777553734	snp	C/G	1.66136e-05	0.00288211	intron-variant	RNF157	GRCh38.p7	17:76161835	CCCCCTGCCGCTCTG[C/G]GGCTTACGCAGTCGG	114804
rs777553951	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76209917	GGCTCACACCACCAC[A/G]CCCAGCTAATTTTTG	114804
rs777561449	in-del	-/TTTT			intron-variant	RNF157	GRCh38.p7	17:76165285	TCTAGCCTTTCTTTC[-/TTTT]ATTTATTTATTTTTT	114804
rs777601995	in-del	-/A/AA			intron-variant	RNF157	GRCh38.p7	17:76174073	ACCTGGAGAATTAAT[-/A/AA]AATAAAAAAAAAAAC	114804
rs777604814	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76218595	TGAGCTATGATCACA[C/T]CCCTGGACTCCAGCC	114804
rs777606862	snp	A/G	1.65173e-05	0.00287374	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161971	CACACCACACACTCG[A/G]CACTGTTATCACTCA	114804
rs777676626	snp	A/G	3.31675e-05	0.00407218	intron-variant	RNF157	GRCh38.p7	17:76159313	ATTCCGGGGGCAACA[A/G]TGTGGAGCACTGGCT	114804
rs777729624	snp	A/G	1.64893e-05	0.0028713	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159414	AGATCGTCCTGACGG[A/G]GGGCAGGTGGCCATC	114804
rs777731791	snp	C/T	1.64822e-05	0.00287068	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154364	TGTGAGTCTATGAAG[C/T]GGCAAAATGAGTAAA	114804
rs777737055	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76182023	TAGGCCTGAGGGACA[C/G]AGTGAAGAGTCAAGC	114804
rs777751180	snp	C/G			intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154634	TGGAAGTAAAAATTA[C/G]TAAATGAAAGAGCAA	114804
rs777752111	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76196826	CTGATTGACAGGGCT[C/G]TACAAAAAGCTGGCC	114804
rs777770130	in-del	-/TTTGG			intron-variant	RNF157	GRCh38.p7	17:76238469	CTAATTAACAAAAGT[-/TTTGG]TTTGGTCTATTGTCT	114804
rs777774824	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76169692	TCAAGTGATTCTCCC[A/G]TCTCAGCCTCCCAAG	114804
rs777834551	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76187606	TTTATTTATTTATTT[A/T]TTTCTGAGACAGGTT	114804
rs777909967	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76234408	AGGAGTAGAACTGCT[C/G]AGTCATCTAGTAACT	114804
rs777991658	snp	C/T	9.89413e-05	0.00703284	intron-variant	RNF157	GRCh38.p7	17:76161515	GCTTCAGAGGGGCCG[C/T]GGTTCCGAGCCCAAC	114804
rs777996057	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76233790	CTTCAGCCTTGGCCT[C/G]CCAAAGTGCTGGGAT	114804
rs778052954	snp	A/C			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145627	ATGTTCCTTGTTTTG[A/C]GAACTTACCCTGGGA	114804
rs778079820	snp	C/G	1.68326e-05	0.00290104	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155562	CGTCCCTTCCCTTAC[C/G]TCTCCTTCTTCTGAG	114804
rs778127260	snp	A/G	4.13693e-05	0.00454785	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76240165	CACCGGACTTGGGCG[A/G]GTAGCGGTACACGGA	114804
rs778170342	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76184736	GTACCCAAATCAAAG[A/G]TATGAGGGAGATAGC	114804
rs778191295	snp	G/T	1.65023e-05	0.00287244	stop-gained, nc-transcript-variant	RNF157	GRCh38.p7	17:76166498	ATGTACCACTAGAGG[G/T]TAAACTTCTCGGTCT	114804
rs778199156	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76193593	TAGTGACTGAAAGGC[C/T]CTCTGAGATTCTCGG	114804
rs778202011	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76192173	AAATTCCTACAACAC[A/G]GATGCTTTAGTTCCA	114804
rs778204656	snp	A/G	1.73453e-05	0.00294489	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155647	CCAGGGGCGATGTAG[A/G]AGCCAGACATGGAGG	114804
rs778215506	snp	A/T	1.64963e-05	0.00287192	missense, intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152446	ACACTCCATACCTAG[A/T]AATGCGCACGTCCTC	114804
rs778220230	snp	A/G	5.04257e-05	0.00502099	intron-variant, utr-variant-3-prime, nc-transcript-variant	RNF157	GRCh38.p7	17:76156353	GACACAACAGGACAT[A/G]GAGCAAGCGCCAGTC	114804
rs778224887	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151402	GGCAACCACAGAGGT[C/T]GTGTGGCTCCAACGC	114804
rs778273258	snp	C/T	0.000230017	0.0107217	intron-variant, nc-transcript-variant, missense	RNF157, RNF157-AS1	GRCh38.p7	17:76147307	AGGACTCCGGAGCTG[C/T]GGCTGTTCAGTAGGA	114804
rs778285342	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76229429	TTTCAACAGATTATT[A/G]TTGAGATCAAGTAAG	114804
rs778293401	snp	C/T	1.67542e-05	0.00289427	intron-variant	RNF157	GRCh38.p7	17:76167843	GTAGCATATCAATAT[C/T]TTAAAATTTACCTTT	114804
rs778319690	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76178909	ATCTTTCCCCAAGAC[A/G]CTCTGGATGCAGCTT	114804
rs778323024	snp	A/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150740	AATTAATACAGTCTC[A/G]CAAATATTTTTTCTC	114804
rs778324977	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76161404	ACGCATGCTCTCAGC[C/T]GGCTTGCTAAATACT	114804
rs778346025	snp	A/G			intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154430	GTATCTAACTCCAGG[A/G]CCTACGTTAATAGCA	114804
rs778418010	snp	A/G	3.66253e-05	0.00427917	intron-variant	RNF157	GRCh38.p7	17:76162518	CACTTGGCCTCCTGG[A/G]AAGAGTACATTCAGA	114804
rs778483493	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76216056	AGATATATTTTCTAT[C/G]CATCAGGAATTATAC	114804
rs778550386	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76209891	CAGCCTCCTGAGTAG[C/T]TGGGACTACAGGCTC	114804
rs778570566	snp	C/G	1.68269e-05	0.00290055	intron-variant	RNF157	GRCh38.p7	17:76162007	TCTTCAGCCACCTGG[C/G]CAAGGAGAAAGAAAT	114804
rs778590454	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76217652	CAGTGGTGGGGGAAA[A/C]GAACTCTACTAAAGT	114804
rs778597805	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76175895	TGAATATATTTGATG[A/G]TAACTGTGGCAATGA	114804
rs778608220	snp	A/C	1.64898e-05	0.00287135	stop-gained, nc-transcript-variant	RNF157	GRCh38.p7	17:76159436	GTGGCCATCACTGCC[A/C]TATGAAGGGAGCATT	114804
rs778613733	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76162729	CAAGGACTACCGATT[C/T]ATAATGAGAAAAAAA	114804
rs778619306	in-del	-/TGT	4.94197e-05	0.00497066	cds-indel, nc-transcript-variant	RNF157	GRCh38.p7	17:76167716	GGCTACCCGAGCATC[-/TGT]GTCAAAGGTGAACTC	114804
rs778622725	snp	C/G			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146718	GGAGCTCCTCCATGG[C/G]ACAAAGCTCCTCCTG	114804
rs778633206	snp	A/G			intron-variant, upstream-variant-2KB, downstream-variant-500B	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76142299	GGAGGCTGGTGCCCA[A/G]ACCATGAAGAAGGCC	114804
rs778659076	snp	C/G	1.65173e-05	0.00287374	intron-variant, missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76155299	CAAAGTTGCTGTCTG[C/G]AGACTCCGCTGGCAG	114804
rs778665284	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76209755	GAAGAAACGGCTACT[G/T]TCATTTTTGTTTTTG	114804
rs778687123	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76183479	TGTTTTTTAGAGGTA[A/G]GGTCTTGCTATGTTT	114804
rs778688742	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76171456	GTCTCCCAAAGTGCT[C/G]GGATTACATGCATGA	114804
rs778699082	snp	C/G	1.65466e-05	0.00287628	intron-variant	RNF157	GRCh38.p7	17:76158342	GGCATGCAGGTAGGA[C/G]GGAAGTCCCTGGAGT	114804
rs778699971	in-del	-/C			intron-variant	RNF157	GRCh38.p7	17:76223265	AATCTCTGCTCGCTG[-/C]CAACATCCGCCTCCC	114804
rs778730975	snp	C/T					GRCh38.p7	17:76194357	CTCATTCAGTTCGCA[C/T]AGAACACCACGCACT	114804
rs778752363	snp	C/T	0.000231073	0.0107463			GRCh38.p7	17:76158414	GAGATGCTGAACCGA[C/T]GGTCTCTGAGAGAGC	114804
rs778776625	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76181830	GGAGAATCACTTGAA[C/G]CCAGGAGGCAGAGGT	114804
rs778813877	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76164365	CCCTAATGCTTTATC[C/T]TTTCGCTTGAAATGT	114804
rs778859088	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76223446	ATCCGCCTCGGCCTC[C/T]CAAAGTGCTGGGATT	114804
rs778913227	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76203770	AAAAAGTTTTGTTGC[-/T]TTTTTTTTTTTTTTT	114804
rs778918909	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76176558	CTTACTATTGATGAC[A/T]GTGGTGGGCTGTCCA	114804
rs778952008	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76208492	AAATGAGACAACACA[G/T]ATGAAAAGCTTAGAA	114804
rs778955713	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76199659	TCAACTTCTCTGGGA[C/G]TGCCCCTTCTTATCA	114804
rs778978418	snp	A/G	1.68906e-05	0.00290603	intron-variant	RNF157	GRCh38.p7	17:76155533	ACAAAGAACAGAGAA[A/G]CCAGGGCGGTTCCCG	114804
rs778986851	snp	A/C/G	0.000149179	0.00863534	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76167048	ATCCACGGTGTGGGA[A/C/G]GGCAGGCAGAACTGC	114804
rs778990420	snp	C/T			missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167708	ATGGTGATGGCTACC[C/T]GAGCATCTGTGTCAA	114804
rs779025039	in-del	-/ATAGC			intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154440	CCAGGGCCTACGTTA[-/ATAGC]ATATATTTCCATCTG	114804
rs779072833	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76178824	GAGGTTATTTTTCTC[A/T]CTTTTTTTTTTCCAG	114804
rs779092826	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76160265	AAGTTTTGATGAACA[A/T]CCTTGAATGCCTTTT	114804
rs779099510	snp	G/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151263	AACTAAATAGAAAAT[G/T]ACTCAAGAAAGCCCT	114804
rs779118026	in-del	-/AAA/AAAAAAA			intron-variant	RNF157	GRCh38.p7	17:76210588	AGCCAGACTCCGTCC[-/AAA/AAAAAAA]AAAAAAAAAAAAAAA	114804
rs779126534	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76211255	TCAACAACTTGAATG[C/T]TCTTAGGCCTGTGCC	114804
rs779143175	snp	A/T	6.549e-05	0.00572195	intron-variant	RNF157	GRCh38.p7	17:76155750	CTTTGGAGACAGGGG[A/T]TGGGGAAAGGAGCCT	114804
rs779243202	snp	A/G	1.69934e-05	0.00291486	intron-variant	RNF157	GRCh38.p7	17:76164703	GAAAGAATAAAAGGA[A/G]GGAAGGACCCTAATA	114804
rs779247134	in-del	-/G			frameshift-variant, nc-transcript-variant	RNF157	GRCh38.p7	17:76159411	CGAGATCGTCCTGAC[-/G]GGGGGGCAGGTGGCC	114804
rs779256737	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76177819	CAGAGATGTCCATAA[A/G]ACCAGCTGCAGAGAG	114804
rs779264431	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76204079	GCCCATAAAAACTTC[G/T]TAATACAATATTCAT	114804
rs779287105	snp	A/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150347	CCCTAGGGAACCCCA[A/G]GGCTTCTCTCTTCCT	114804
rs779322381	snp	C/T			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76212645	GGCAGACAGATCGCC[C/T]GAGATAAGGAGTTCG	114804
rs779347131	snp	A/G	2.28741e-05	0.0033818	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF157, RNF157-AS1	GRCh38.p7	17:76145186	AGCAGCTGAGTGAGG[A/G]TGGATGGAATGCAGG	114804
rs779407082	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76238984	GCGGGCAGGTTCATC[C/G]TCTGGCCCCTGCTTT	114804
rs779460480	in-del	-/AG			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76147826	CAAAAAATGGAGCAC[-/AG]AGATTCAAAATCCTT	114804
rs779482691	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76163969	TTAAAAGAGAGGCGA[A/G]TAATTAACCTAAAAG	114804
rs779497189	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76225465	CCTTCCAGATTTTTT[A/T]ATACATATACAAATA	114804
rs779590121	in-del	-/AGA			intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213919	GCCCAGAGACGGCAT[-/AGA]AGCTCTGTGCCCCTT	114804
rs779615337	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76229365	CAGGACAAATTATTT[A/G]AACTTTTTGAGCTTT	114804
rs779647631	snp	A/G	9.90148e-05	0.00703545	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76158426	CGACGGTCTCTGAGA[A/G]AGCTGTGTCTCCGAC	114804
rs779687905	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76240010	CGGCCTTCTCGAAGA[C/T]CTCCCGCGCTCGAAG	114804
rs779726707	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76193859	GATTAGCGCCTGGCC[A/G]AGGGCTGCTGATGCA	114804
rs779730232	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76227769	GTAGTCCCAGCTACT[C/T]AGGAGGCTCAGGCAG	114804
rs779733866	snp	A/T	1.6857e-05	0.00290314	intron-variant	RNF157	GRCh38.p7	17:76155544	AGAAGCCAGGGCGGT[A/T]CCCGTCCCTTCCCTT	114804
rs779768168	in-del	-/C			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146351	GGTGAGTATCTGACT[-/C]CCTAGAATAGCCTGT	114804
rs779796224	snp	C/T	1.651e-05	0.0028731	synonymous-codon, intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76152461	AAATGCGCACGTCCT[C/T]TGGCCTGTAACGGAG	114804
rs779797607	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76224079	ACTGAGGGAGCCCTA[C/T]CCTATCAATGGCAAT	114804
rs779891091	in-del	-/CACGT	1.64969e-05	0.00287196	frameshift-variant, nc-transcript-variant	RNF157	GRCh38.p7	17:76159485	CAAGCACGTGAAGTG[-/CACGT]GAGGAACTGCTGGGG	114804
rs779918877	snp	A/G	1.64781e-05	0.00287033	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154236	CTTAAAGAATACCCA[A/G]GAAAGAAAGATAACT	114804
rs779920916	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76195154	CAAATGGCAGAAACA[C/T]ATTCATGTCACAGAA	114804
rs779944724	snp	C/T			intron-variant, utr-variant-5-prime	RNF157	GRCh38.p7	17:76175767	ATTTCAAAAAAAAGA[C/T]GCGTCTTTTCCCTTA	114804
rs779954487	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76209283	AGGCTGCTACCTAGC[A/G]TTTCAGAAAGAGCTC	114804
rs779968677	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76173911	GCACAACTCTCCTAA[-/T]TAAGTGAGGAAACTG	114804
rs779976981	in-del	-/TA			intron-variant	RNF157	GRCh38.p7	17:76236740	TTATCAACAGGAGAC[-/TA]TGTAAAAAAAAAGAT	114804
rs780005219	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76207579	GCATTTATAGCTTAA[A/T]ATAACAATTCATTTT	114804
rs780039427	snp	A/T			utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144563	CCACCCGCCTCGGCC[A/T]CCCAAAGTGCTGGGA	114804
rs780063424	snp	C/T			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149987	GCAGTGAGCCGAGAT[C/T]GCGCCACTGCACTCC	114804
rs780091909	snp	A/C	1.72341e-05	0.00293543	intron-variant	RNF157	GRCh38.p7	17:76162547	GAATTTTGGGTAAAA[A/C]TTACCTTAGAATCTT	114804
rs780098178	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76187472	TACAGGCATGAGCCA[C/T]GGCGTCTGGCCAGGA	114804
rs780115148	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76178582	CTGAGCCGAACCTGT[A/G]CAAGGCACCACTGGC	114804
rs780167624	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76223816	TATATTTTTGGAAAC[A/G]AAAGCAAAATAACTC	114804
rs780190111	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76189957	CTCCAGCCCTGTAGA[C/G]CTTCCAGCACCTCCC	114804
rs780190622	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76225378	CCAAAAAAATTAGTA[C/T]ATATAAGTTAATAAT	114804
rs780214442	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76171423	TGAACTCCTGACCTC[A/G]GTGATCCGCCCGCCT	114804
rs780231234	in-del	-/AATCCAAAGTCAACTA			intron-variant	RNF157	GRCh38.p7	17:76160796	TAGAGAATCCTTTCC[-/AATCCAAAGTCAACTA]AATCCAAAGTCAACT	114804
rs780243656	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76201323	GACCCTAGTCTCTAC[-/A]AAAAAAAAAAAAAAA	114804
rs780255865	snp	C/T	4.1401e-05	0.00454959	missense, intron-variant, utr-variant-3-prime, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145302	CTGCTGGATGACAAG[C/T]GCCGGCGCTGGGCAT	114804
rs780262223	in-del	-/AT			intron-variant	RNF157	GRCh38.p7	17:76182761	TTCAGGCCTCGTCTC[-/AT]ATATATATATATATA	114804
rs780280482	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76221769	ATGTCAAACAACAAA[C/T]GGGTAAACAAAATGT	114804
rs780293331	snp	A/C/T	3.29583e-05	0.00405934	missense, upstream-variant-2KB, nc-transcript-variant	RNF157	GRCh38.p7	17:76212432	AACCTTCAGGATGAG[A/C/T]TGAGTCAAACTTCTC	114804
rs780376360	snp	C/T	1.65072e-05	0.00287286	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159356	AGACTCTTTTTGAGT[C/T]TGAGTCCCTGACTGC	114804
rs780396505	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76157940	CCTAGGGCCCTCTCT[A/C]CTCGTATATCTGCAT	114804
rs780418098	snp	A/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151556	TCTGTCGTGAAACCC[A/G]GAGGGGACATTTGAC	114804
rs780420409	snp	A/G	5.17639e-05	0.00508717	intron-variant	RNF157	GRCh38.p7	17:76164827	AAAGTTATGACAAGG[A/G]AGGGAGGGTAATAAA	114804
rs780467909	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76202656	TTTTTTTTTCAGGCT[C/G]TGAATAGTTCTAGGG	114804
rs780474329	snp	C/G	1.65373e-05	0.00287548	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167105	AGTCTCCGACTGGAG[C/G]CTGTTGTCTTTGGGA	114804
rs780475505	snp	C/T	3.29843e-05	0.00406092	intron-variant	RNF157	GRCh38.p7	17:76165564	AAAGAAACAAAGGCA[C/T]GTGAGTGAAGAAGCC	114804
rs780487664	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76177538	GGGAAGGGGGAGAGG[C/T]GAGGGGGTGCTGAGG	114804
rs780488653	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76170217	CTCAACATCCAGTAT[G/T]CCAGGATCCACTCAC	114804
rs780488971	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76219423	TATGCTACCATGTGT[A/G]TAAGGAAGAGTGGCT	114804
rs780493285	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76203356	GGAAATTGAGACTCA[C/T]TGATTGGCCATCGTC	114804
rs780529932	snp	A/G	3.30524e-05	0.00406511	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76161638	CGGATCTGAAGCAGT[A/G]CCCGGAAGGCTGTGA	114804
rs780581048	snp	A/G	1.67438e-05	0.00289338	intron-variant, downstream-variant-500B	RNF157	GRCh38.p7	17:76156175	GGGCTGGGTAAGGGG[A/G]AAGGACATGCAGCCA	114804
rs780581376	snp	C/T	3.35593e-05	0.00409616	intron-variant	RNF157	GRCh38.p7	17:76161806	TCCTCTTGTCCCCTC[C/T]CCCACCCACCAGTCC	114804
rs780587712	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76181706	TGAGGTCCAGAGTTT[A/G]AGACCAGGCTGGCCA	114804
rs780626402	in-del	-/C			intron-variant	RNF157	GRCh38.p7	17:76193894	AATGCTGCCCTGCTA[-/C]CCCCTCCCACCTCCA	114804
rs780629460	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76206253	AAAAAAAGGCCAGGA[A/G]GGAGTCAAGGCATTA	114804
rs780639601	snp	A/G	3.2956e-05	0.00405918	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154358	AGGCCCTGTGAGTCT[A/G]TGAAGCGGCAAAATG	114804
rs780699545	snp	A/G	1.65963e-05	0.0028806	intron-variant	RNF157	GRCh38.p7	17:76159305	CATCAAGGATTCCGG[A/G]GGCAACAGTGTGGAG	114804
rs780700739	snp	A/G	3.31e-05	0.00406803	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76167119	GGCTGTTGTCTTTGG[A/G]AATGTAGCTATTGAT	114804
rs780738251	snp	A/G			missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159503	GGAACTGCTGGGGAC[A/G]GGGTGAGGGGCCCGT	114804
rs780753021	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76226488	GGTCATCTGGCATGG[C/T]TTCCAGGTCATCTAT	114804
rs780754042	snp	A/G	4.97179e-05	0.00498562	intron-variant	RNF157	GRCh38.p7	17:76161650	AGTGCCCGGAAGGCT[A/G]TGAAGGAGAAAACAG	114804
rs780758771	snp	C/T			upstream-variant-2KB	RNF157	GRCh38.p7	17:76241364	GTGGGAAGCTTGGGC[C/T]GGCGGAAGACGTCAT	114804
rs780774947	snp	A/G	1.64776e-05	0.00287028	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154266	TAAAGGAAGTAAAGG[A/G]CCAGATCTTTTACCA	114804
rs780815650	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76188278	TGGGATCACTCCACT[A/G]CCCCATGTGGTCACC	114804
rs780851813	snp	C/T	2.33609e-05	0.00341759	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76173773	GGGTTCTTGGGGAGG[C/T]GGGGCGGCGTAAGGA	114804
rs780859820	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76206351	AACTCAATAAAGGAG[C/G]AGAAAAGCAACACCA	114804
rs780861654	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76219855	ACAGTATTTTCTTCC[A/G]AGAATGTGGCATTAA	114804
rs780901316	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76157529	TCCTCCATAACACAT[C/T]TTCTGATTTCCTCCA	114804
rs780904433	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76216781	CTGTGGTCCCAGCTA[C/T]TCAATAGGCTGAGGT	114804
rs780916025	in-del	-/CTCT			intron-variant	RNF157	GRCh38.p7	17:76193592	ATAGTGACTGAAAGG[-/CTCT]CTGAGATTCTCGGTT	114804
rs780944374	snp	C/G	3.31011e-05	0.0040681	intron-variant	RNF157	GRCh38.p7	17:76167613	TGGCCTGGTAATAAT[C/G]TGGGAAGGAAGTGGC	114804
rs780951945	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76233457	ATCTAAGAACTCTTC[A/G]CCCAATCCAAATCAA	114804
rs780976370	snp	A/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151440	CACGTCGCTGAGCGA[A/G]TAAAGCACTGGACCC	114804
rs781012700	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76172240	GACTGCTTGAGCCCG[A/G]GAAGTTAAGGCTGCA	114804
rs781072314	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76155399	TTCAGAACAAAATTG[A/G]TGTCAAATAGGAGGG	114804
rs781082080	in-del	-/A	6.29723e-05	0.0056109	intron-variant	RNF157	GRCh38.p7	17:76173694	GCCCCAGCCTCTGGG[-/A]AACTTACTTGACGAG	114804
rs781102576	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76174970	ATTACAAAGTAATAT[A/G]TGTTTAAGCAGAAAA	114804
rs781147449	snp	C/G	1.65291e-05	0.00287476	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76158481	TCTTCATGCAGCACG[C/G]AAGAGTTTTGGGAAG	114804
rs781150926	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76172700	TAATGCTAATAAGGC[C/T]GTTCTATACAAGCAT	114804
rs781160723	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76184105	CTGAGGCAAGATAAT[C/T]ACTTGAACCTGGGAG	114804
rs781162843	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76166926	CAAGCATCCGAGCAG[A/C]CCCTTTGCTGTCAGA	114804
rs781182106	snp	C/T			utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76143659	GCCACAACCACTAGG[C/T]AGTGAGACAGTCACT	114804
rs781190730	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76158884	GGGAAAAACCACTGC[C/T]ATTTACAGGGTCTCA	114804
rs781191907	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76224304	GTTCCCTAAATTATG[A/T]CTGCCTCAATAAGAT	114804
rs781197498	in-del	-/CA			intron-variant	RNF157	GRCh38.p7	17:76157827	GGTCTCTGTGGGACG[-/CA]CAGAGTAGAAAATTC	114804
rs781223348	in-del	-/TAA			intron-variant	RNF157	GRCh38.p7	17:76220385	GTTCGTAATGATATC[-/TAA]AAAAAAAAAAAAAAA	114804
rs781223598	snp	A/C	3.74721e-05	0.00432836	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145384	TGAACATTACAGGAG[A/C]CAGACCTTTGGCCAA	114804
rs781234437	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76218695	TCCCAGCACTTTGGG[A/T]GGCCAAGGTGGGCAG	114804
rs781265282	snp	C/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76149096	ACACACTACTCCCCA[C/G]TGAAAAACCAAAAAT	114804
rs781280467	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76157795	AGAGAGAAGCTGCAT[A/G]AACCTTTGTTAAGTG	114804
rs781294436	snp	C/T			utr-variant-3-prime, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144127	AATGCCACCTCCCAA[C/T]TGAGTGAGGATGAAT	114804
rs781316812	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76235498	CCACTGCGCCCAGCC[A/G]TAAATTGCATATTTT	114804
rs781324342	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76234577	CTAGTGGGTGTGAAG[C/T]GGTATCTAATTGTAG	114804
rs781334300	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76202582	ACGTCCACACCTCAT[C/G]TGTGGACCACATCAT	114804
rs781340490	snp	G/T	5.75457e-05	0.00536372	utr-variant-5-prime, nc-transcript-variant	RNF157	GRCh38.p7	17:76240242	GTCAGGGCCCCCATG[G/T]CCGCTGCGGCTGCAG	114804
rs781402541	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76197471	TGTTTGAGACCACCC[C/T]GGGCAACACAGCAAG	114804
rs781498888	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76201684	TATATTATTTTTATC[C/T]GAAATGAAATCAGAC	114804
rs781522733	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76227552	AAACTAATGCACAGA[A/G]GTTAAATAATCTGTC	114804
rs781546456	snp	A/C			intron-variant	RNF157	GRCh38.p7	17:76176629	GCAGGGAGCAGACAG[A/C]CAGCCCCTCCACAGC	114804
rs781548259	snp	A/G	1.64961e-05	0.00287189	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76166494	CGGCATGTACCACTA[A/G]AGGGTAAACTTCTCG	114804
rs781548681	snp	A/C	1.64895e-05	0.00287132	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159449	CCATATGAAGGGAGC[A/C]TTCCTGAGAGGTGGC	114804
rs781601742	snp	C/T	1.65679e-05	0.00287814	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76159540	CCTCCAGAAGAGATA[C/T]TACTTCATAGCCTGG	114804
rs781613149	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76180801	AGTATACAGTTCAGC[A/G]GCATTAAGTAACATT	114804
rs781619417	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76188492	TCCCTGAAGAATAAA[G/T]AGGTGTCTTAGCATT	114804
rs781620543	snp	A/C	4.95413e-05	0.00497677	synonymous-codon, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156256	CGTCCCTGTGCAAGA[A/C]GACTGGTCAATAGCT	114804
rs781626100	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76220385	GTTCGTAATGATATC[-/T]AAAAAAAAAAAAAAA	114804
rs781640190	snp	A/C	5.01651e-05	0.005008	intron-variant	RNF157	GRCh38.p7	17:76161820	CTCCCACCCACCAGT[A/C]CCCCTGCCGCTCTGG	114804
rs781699657	snp	A/G	1.64822e-05	0.00287068	missense, upstream-variant-2KB, nc-transcript-variant	RNF157	GRCh38.p7	17:76212441	GATGAGTTGAGTCAA[A/G]CTTCTCTCCTCCCAT	114804
rs781711226	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76168214	TTTTTCAGTTTCAGG[C/T]GCTATCTATGGGTTT	114804
rs781722764	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76181290	GAAGCTAGCCAAAAA[-/T]CTCCAATGGCGCCCT	114804
rs796177700	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76160384	CTGCTGTTTTTTTTT[-/T]CAGTGCCTTTTCTAG	114804
rs796280646	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76160276	ACATCCTTGAATGCC[-/T]TTTTTTTCAAATTAT	114804
rs796350865	in-del	-/AGAGAGAGAGAAAGAGAA			intron-variant	RNF157	GRCh38.p7	17:76230869	AAAAAAGAGAGAGAG[-/AGAGAGAGAGAAAGAGAA]AGAGAGAAAGAGAGA	114804
rs796441485	snp	C/G			intron-variant	RNF157	GRCh38.p7	17:76186455	GAGGTTGCAGTGAGC[C/G]GAGATCACACCACTG	114804
rs796477727	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76207067	TCTTCCACCATCTTT[C/T]TGTATATACACACAC	114804
rs796590042	in-del	-/C			intron-variant	RNF157	GRCh38.p7	17:76235320	CTCCTGCCTCAGCCT[-/C]CCGAGTAGTTGGGAC	114804
rs796647742	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76227156	AGTCTCACTCTTGTC[A/G]CCTAGGCTGGAGTGC	114804
rs796668304	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76233853	TTGAAAATAGCTTTG[C/T]GGAGATACAATTTAT	114804
rs796697054	in-del	-/A			intron-variant	RNF157	GRCh38.p7	17:76164611	TTTTCTTCTTTGATT[-/A]AAAAAAAAAAAAAGA	114804
rs796751666	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76172495	ACTTAGGAGGATAAG[A/G]CAGAAGAATCCCTTG	114804
rs796792552	snp	G/T			intron-variant	RNF157	GRCh38.p7	17:76206073	TCTCTCTATAGAAAT[G/T]TTTTTTAAAAAGCCA	114804
rs796827458	snp	A/G			intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151547	AGGACAATTTCTGTC[A/G]TGAAACCCGGAGGGG	114804
rs796920901	in-del	-/T			intron-variant	RNF157	GRCh38.p7	17:76164890	TACAGTCGCCCTCCC[-/T]GATCTGCAGTTTCAT	114804
rs796964176	multinucleotide-polymorphism	CGT/TGG			intron-variant	RNF157	GRCh38.p7	17:76163680	TATATCCCACTCTCC[CGT/TGG]TTAACAGTCTGTTGC	114804
rs796991170	in-del	-/CTT			cds-indel, intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76144321	CAGATTCAAGGGCTC[-/CTT]CTTTTTTTTTTTTTT	114804
rs797006239	snp	A/G			intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76146739	GCTCCTCCTGGGCAG[A/G]GGCCGTGACTTCTTC	114804

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