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

RNF111

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs142781933	in-del	-/TG			intron-variant	RNF111	GRCh38.p7	15:58989068	CTTTCCCATTTTTGT[-/TG]TGTGTGTGTGTGTGA	54778
rs142809582	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59043154	AAAGTGTACAATTTA[A/G]TAATTTTTTTTTTTT	54778
rs142811419	in-del	-/GTTT			intron-variant	RNF111	GRCh38.p7	15:59090220	TTTTTTTGTTTGTTT[-/GTTT]GTTTGTTTGTTGTTG	54778
rs142850130	in-del	-/TTCA	0.00874735	0.0655527	intron-variant	RNF111	GRCh38.p7	15:59029834	TTCATTTTTTTAGTG[-/TTCA]TTCATCTATAAACTT	54778
rs142855631	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58994677	GAGACGAGGTTTCAC[C/T]CTCTTGGCCAGGCTG	54778
rs142867281	snp	C/T	4.94727e-05	0.00497332	synonymous-codon	RNF111	GRCh38.p7	15:59075971	GGCATTGCCAGTGGA[C/T]CTGAGCAACAGTGGT	54778
rs142903827	snp	G/T	0.00835141	0.0640778	intron-variant	RNF111	GRCh38.p7	15:59053062	TTAGAATCTACTTGT[G/T]TCAATATGTTACTCA	54778
rs142916216	snp	G/T	0.0029633	0.038378	missense	RNF111	GRCh38.p7	15:59052312	GTTTCCAGGAAGTAT[G/T]GATGAAGATGTTGTG	54778
rs142927737	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59023746	TTTTTCTTCCAGATT[G/T]TAATGAGAATGCCTA	54778
rs142933797	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59087322	TTCTGAGAACTGGCT[G/T]GAAAAGTTGAGAAAC	54778
rs143031851	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59008804	TTAAAAAAAATCTTT[C/T]GTGGTTCTTTTAGGG	54778
rs143052199	snp	C/G	3.2956e-05	0.00405918	missense	RNF111	GRCh38.p7	15:59076026	TTTCATGGAGCATCT[C/G]CATTTGACCCCTGCT	54778
rs143074239	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022508	CTTTCCTTTTTATAG[C/G]ATGAGCAGTAATATC	54778
rs143079828	snp	G/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59001135	CCTCGTGGTTATCTG[G/T]GGGAAGAGCATTCAA	54778
rs143083683	snp	A/C/T	4.94436e-05	0.0049719	synonymous-codon	RNF111	GRCh38.p7	15:59031338	GACCATTTTGAATGC[A/C/T]AAAAGTAGAAGCCAT	54778
rs143099887	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59012794	CCTGGGCTGGAGTGC[A/G]GTGGCACAATCTCAG	54778
rs143121643	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59024462	CTAGCAAGATCTTTT[C/T]AGCAAGTACTTTAAG	54778
rs143146798	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59055112	CATAAACTAGCTCAC[A/G]CAAGTAATATTTCTT	54778
rs143147272	snp	A/G	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:59002951	CTTAGAGAGGATCCT[A/G]TTGATGGTCAACCTT	54778
rs143179084	snp	G/T	0.0562307	0.157967	intron-variant	RNF111	GRCh38.p7	15:59006826	GAGTCTTGCTCTGTC[G/T]CCCAGGCTGGAGTGC	54778
rs143223865	snp	C/G	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:59028519	GAATGTGGTCTCTCT[C/G]TCATAGTGTGAGTAA	54778
rs143244168	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59001743	TACAAAACATACATT[A/G]TCATGGGATTTTATT	54778
rs143246180	snp	C/G	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59032678	CACCTGCCTTGGGCT[C/G]TCAATATTTTTTCTT	54778
rs143248976	snp	C/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59002648	TTAGGCAAGTCACTT[C/T]TGTAATCTTCAGTTC	54778
rs143250981	snp	C/T	0.0154538	0.0865337	intron-variant	RNF111	GRCh38.p7	15:59060376	TTGGGAGGCCAGGGA[C/T]GCAGATCACTCGAGG	54778
rs143311514	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59004308	AAGGAACTTGCTGTT[G/T]AGGTTTACTGAAACT	54778
rs143313414	snp	A/C	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59011588	TTTTTCCTGAGGCCC[A/C]TCTTCTTGGTTTATA	54778
rs143319413	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59035007	TCACAGTTCCACATG[A/G]CTGGGGAGGCCTCAC	54778
rs143393452	snp	A/G	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:59029777	GAAGATTTCTAGGGT[A/G]CTGGTTATGTTGTTT	54778
rs143490471	snp	G/T	0.00716266	0.059414	intron-variant	RNF111	GRCh38.p7	15:58996393	TCCTGGCCAACCTGA[G/T]GAAACCCTGTCTCAA	54778
rs143492727	snp	C/T	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59050235	ATGCTCGACTAATTA[C/T]TGTATGAGCAGTAGC	54778
rs143494874	snp	C/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59019804	TCTTTACTGAAAATA[C/T]AAAAATTAGCCAGGT	54778
rs143497121	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59082224	TTTAGTAAAATCTGA[C/G]CAGTTTTACCATATG	54778
rs143498832	snp	A/G	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59078309	GTTTGTGGTCTTGAT[A/G]AAGTGATAAAACAAC	54778
rs143539102	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59044219	TATTATTAATAGAGA[C/T]GGGGTTTTGCCATGT	54778
rs143562149	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990517	TAGCCGAGCTTAGTG[A/G/T]TGTGCGCCTGTAGTC	54778
rs143566574	snp	C/T	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:59089947	AGGGTCAAAAGTTAC[C/T]GAAATATTTAAAGAT	54778
rs143591397	snp	A/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:58993450	GGCTGAGACAGGAGA[A/G]TTGCTTGAACCCAGG	54778
rs143594527	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59000545	GGGGAAACCCTGTCT[C/T]TACGAAAAATACAAA	54778
rs143629978	snp	C/T	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59037897	AGGAAACGTAAATGT[C/T]AAATATGCTCCTAAA	54778
rs143630700	snp	G/T	0.00438332	0.0466095	intron-variant	RNF111	GRCh38.p7	15:59017044	AGGGCTCCCACTGAT[G/T]CTATATTACGGTGAA	54778
rs143642836	snp	C/T	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59078510	CACACCTGTGAACAA[C/T]CCTTGTACTCCTGCC	54778
rs143673628	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime	RNF111	GRCh38.p7	15:59095145	ACTGTATTTTTGCAT[C/G]GTTCCTTGTATTGCA	54778
rs143678982	snp	A/T	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59041037	CTTCTCTTACTCAAA[A/T]GTGTCTCTTGCTTTT	54778
rs143685164	snp	C/T	0.00716266	0.059414	intron-variant	RNF111	GRCh38.p7	15:59083139	GGAGCAAGATTCTGC[C/T]GCTTAAAAAAAAAAA	54778
rs143738743	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58991521	GCCATGAGGAAAATA[G/T]GACCATGTGATACGG	54778
rs143743648	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59068748	TCATCTTTTAAAATT[C/T]TGATGGTATGTCTTC	54778
rs143779952	snp	A/G	0.000445085	0.0149112	synonymous-codon	RNF111	GRCh38.p7	15:59031362	AAGCCATAGTGCACG[A/G]TCTCATAAGTGGCCT	54778
rs143808671	snp	A/G	0.00835141	0.0640778	intron-variant	RNF111	GRCh38.p7	15:59018169	ATTATTATCATTTTC[A/G]AGCATTAAAATTTAT	54778
rs143816615	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59081767	TGCAGTGATTCACCC[A/C]TATAATTCCAACACT	54778
rs143821180	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59081365	AACTCTGAAATCCAA[C/G]TAGGCATGGTGGCAT	54778
rs143841791	snp	A/G	8.2373e-05	0.00641714	synonymous-codon	RNF111	GRCh38.p7	15:59094828	AGTGTGTGTTGACCA[A/G]TGGTTGATTACCAAT	54778
rs143843255	snp	C/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:58989537	TGCAGATCCTTCTGT[C/T]ACTTCTTAACTTTTG	54778
rs143849860	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59013364	TCCAGATAATATTTC[A/G]TTGTAGACTCTGGTT	54778
rs143854635	snp	A/G	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59073782	ACTCCTTTCTGGAAG[A/G]TTTTCAATTTACTTT	54778
rs143901550	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59061953	CTCATCCCCCCTTTC[A/G]CTAGCCCATTTCATA	54778
rs143902713	snp	C/T	0.0839998	0.186933	intron-variant	RNF111	GRCh38.p7	15:59064331	ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT	54778
rs143935904	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59028191	GTAACCACATTCTAT[C/G]TATGTAGATTTGCCT	54778
rs143995225	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59017122	CACAATAAATGTACT[A/C]GGATCATCTCAAACC	54778
rs144002410	snp	C/G	0.00835141	0.0640778	intron-variant	RNF111	GRCh38.p7	15:59061308	CTATGTTCTCCACAA[C/G]CCGTCCTTATCTTGT	54778
rs144032682	snp	C/T	0.029116	0.117091	intron-variant	RNF111	GRCh38.p7	15:59066381	TTTGGGAGGCTGAGG[C/T]GGGCAGATCACCTGA	54778
rs144032765	snp	C/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59027158	CATGATCTCCATTAT[C/T]AACATGAGGACTTAG	54778
rs144067472	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59029281	ACCTGTGTTTTATCA[C/T]TGTGACTTCTGTGTT	54778
rs144080108	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096308	TGCATCCAGTCAGTA[A/G]TATCACTGTCTGTAT	54778
rs144107264	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59062641	AGCCTATAGTGTTGG[C/T]CGGTGGATTTGCCTA	54778
rs144140273	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59046429	CACTCCTGGGCTCAA[A/G]TGATCTGCCCACCTC	54778
rs144161266	snp	C/T	0.00716266	0.059414	intron-variant	RNF111	GRCh38.p7	15:59088452	AATTTAAGTAATAGG[C/T]TATTGAAGGTTAAAA	54778
rs144276574	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59015295	AGCATGTTAGAGATA[C/T]TGTCATGTTTTGTGT	54778
rs144278641	snp	G/T	0.00557542	0.0525036	intron-variant	RNF111	GRCh38.p7	15:59046948	TCTCGGCTCACTGCA[G/T]ACTCGGCCCCCTGGT	54778
rs144285987	snp	C/T	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:58998386	GTTATTTTTCCTTAT[C/T]CTCTCCCTCCTCCCA	54778
rs144289361	snp	C/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59053171	ACTCAGTAATTTTAT[C/T]GGTGCTCTGAACTAA	54778
rs144347835	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59006358	GTGCTCTTTTGCCAT[C/G]AGCCACCCACATCTC	54778
rs144358000	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59091755	GGACCAGTTTTCATG[A/G]AAGACAATTTTTCAT	54778
rs144416674	snp	A/G	0.0452528	0.143452	upstream-variant-2KB	RNF111	GRCh38.p7	15:58986795	GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCC	54778
rs144419270	snp	C/T	0.0689305	0.172377	intron-variant	RNF111	GRCh38.p7	15:59010668	TGGCCTCCCAGAGTG[C/T]TGGGATTACAGTCAT	54778
rs144424985	snp	A/G	0.0228947	0.104514	intron-variant	RNF111	GRCh38.p7	15:59039622	GCCATCCTAGTAGTC[A/G]TTGATAACTTCCTTC	54778
rs144425776	in-del	-/TACAG	0.0154538	0.0865337	intron-variant	RNF111	GRCh38.p7	15:59083678	ATGGTTGAATGTCTT[-/TACAG]TATAAGAGTAAATGA	54778
rs144426426	snp	A/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59044467	ACCAGGAAATAGAAA[A/T]GGGCTTTGAAGAGTT	54778
rs144459354	snp	A/T	0.00835141	0.0640778	intron-variant	RNF111	GRCh38.p7	15:59029002	CCAGGCTGATCTCGA[A/T]CTCCTGGCCTCCAGT	54778
rs144464225	snp	A/C	0.00358779	0.0422022	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096735	TATGTCTGCCATCTT[A/C]CTGGGGAAAAGAGCA	54778
rs144504098	snp	C/T	0.0217236	0.101931	intron-variant	RNF111	GRCh38.p7	15:59037664	CAACATGGAGAAACC[C/T]CGTCTCTACTAAAAA	54778
rs144525991	snp	C/G	0.00716266	0.059414	intron-variant	RNF111	GRCh38.p7	15:58990919	TACATCCTACAGATT[C/G]TTGGTAACAGCTGGC	54778
rs144536525	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59070679	ATACAAAAGAAAGGA[A/G]CTCCTCCTTTTCTCT	54778
rs144562709	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59040035	TTCTTTTATTGGGAG[A/G]TGATAGAGACTACAG	54778
rs144576794	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59072394	AGTTTATGTGATGTA[C/G]TAATGTAATATATTA	54778
rs144614737	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59082396	TCTAAAGATATCAAA[G/T]ATTTGAATGTTACTA	54778
rs144710041	snp	C/T	0.000296506	0.0121723	missense	RNF111	GRCh38.p7	15:59081182	CACACCAGCCAATTT[C/T]GCACCATATTCCAGC	54778
rs144726768	snp	C/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:58997250	TGTATTTTATATGTG[C/G]ATCCAGAGTAGTGGT	54778
rs144726783	snp	A/G	0.0228947	0.104514	intron-variant	RNF111	GRCh38.p7	15:59027887	CTGGAGTGCAGTGGT[A/G]TGATCTCAGCTCACT	54778
rs144731042	snp	C/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59023582	CCTGTCTTACTGTTG[C/T]CAGTGGTTTTCTACT	54778
rs144739027	snp	A/C	0.0379877	0.132479	intron-variant	RNF111	GRCh38.p7	15:59094198	TATATAACAATTATT[A/C]CGTGAAAAAAGTATT	54778
rs144747860	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:58997814	GTGAGACTCCATCTC[-/A]CAAAAAAAAAAACAA	54778
rs144778821	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59092914	CTAAGGCAGGAGGAT[A/G]GCTCAAGCCCAGGAG	54778
rs144790036	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59000338	TTGGCTCATTTTTCT[A/G]TTTTTAGTAGAGACG	54778
rs144803836	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59057965	TAGAATCCATATTGT[G/T]TCAGACAGTGTGGTT	54778
rs144835824	snp	A/C	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:58998566	ATTAGCAAACTAGTC[A/C]CTTCTTTCATGGAAC	54778
rs144870511	snp	A/G	0.00478085	0.0486577	intron-variant	RNF111	GRCh38.p7	15:59025271	GTAATAAGTTTATCA[A/G]GGGTCCCACTCTTCT	54778
rs144886792	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59090167	TTTTCAGGAAGAACA[A/C]ATCATTCGAATGGGA	54778
rs144899740	snp	A/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59047576	ATTTTGTGTTTTTTT[A/T]AATTATTATTATGTT	54778
rs144912652	snp	G/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59023932	GACTTTCTGGAAGGT[G/T]CAACCACTTTCCTAT	54778
rs144914729	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59087822	GGGTGAACTGTAATA[C/T]GGTCAGTATGGTGTC	54778
rs144922501	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59094173	TTAAACAGTAGCACA[A/G]TATTAAGTGTATATA	54778
rs144948432	snp	A/G	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:58999640	TGTGCCCGGCCTATT[A/G]CTGCAGTTTTAAAAT	54778
rs144955486	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59054933	TATCCTGGAGCCTTA[A/G]GACTGCATATTCTAC	54778
rs144972496	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59026324	TCGTATTTTCTTAGT[A/G]CAAGGTTTACTAATA	54778
rs144974495	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58995443	CCAAGTGGGCTCCTG[C/T]GTCTTTTTAACATAA	54778
rs145042466	snp	C/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:58988987	TCTTGTTTTAGGGGC[C/T]TCTTGAACTAAAAAG	54778
rs145044983	snp	C/T	0.0422008	0.138995	downstream-variant-500B	RNF111	GRCh38.p7	15:59097687	GATCGAGACCATCCT[C/T]GTTAACATGGTGAAA	54778
rs145161897	snp	A/G	0.00716266	0.059414	intron-variant	RNF111	GRCh38.p7	15:59073541	AGAAGCAACTCATTC[A/G]GCTTTTATCAGGATT	54778
rs145167389	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59040810	TTCTGTGTGGTTATG[C/T]CACCAATTTCACATG	54778
rs145184660	snp	A/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59074926	ATTGGCCTAATTTCA[A/G]TGTTGTTGTGTCTCA	54778
rs145192451	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58989384	TGACTTTATCATCTC[C/T]CTCCTGCTCATTTGT	54778
rs145204570	snp	A/G	1.66181e-05	0.00288249	missense	RNF111	GRCh38.p7	15:59055770	GAGCCACGGAACCGC[A/G]GTAGGATTTCTACTG	54778
rs145213358	snp	C/T	0.00597247	0.0543191	intron-variant	RNF111	GRCh38.p7	15:59011205	TCACTGTCTTATCCT[C/T]CCTGGAAAACTTTTC	54778
rs145261691	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59033323	TATTTTTCTCTTTTT[-/T]GCCAGAACCCTAAAC	54778
rs145283259	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59011048	TCTTGAAGATGAAAA[A/G]TTGTCTATCAGAAGA	54778
rs145318126	snp	A/C	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59014276	CTTGTATTTTCAATG[A/C]CCTGGTGAAATCAGC	54778
rs145365562	snp	A/G	1.64789e-05	0.0028704	missense	RNF111	GRCh38.p7	15:59052361	ACTCCCCAGGTTACT[A/G]CCAATGAAGAAATTA	54778
rs145404913	snp	A/G	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59001416	CTGCTATTAGTTCCT[A/G]TTTTTGTTGTTGATT	54778
rs145411225	snp	A/G	0.0119091	0.0762411	intron-variant	RNF111	GRCh38.p7	15:59022754	ATTGGCAGATAATAG[A/G]AAACTTCTCATTATT	54778
rs145414874	snp	A/G	0.0146672	0.084371	intron-variant	RNF111	GRCh38.p7	15:59083935	GAGCAATTAGAATTT[A/G]TGGAGAAGGTGATGG	54778
rs145446342	snp	C/G	0.00636936	0.0560724	intron-variant	RNF111	GRCh38.p7	15:58995883	CGTTTTCCATGGAAC[C/G]CTGGTTCCTTTTAGT	54778
rs145457741	snp	A/G	0.000115419	0.00759581	missense	RNF111	GRCh38.p7	15:59031367	ATAGTGCACGGTCTC[A/G]TAAGTGGCCTCGGAC	54778
rs145480288	snp	A/G	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59025159	CAAAGTGCAGGGATT[A/G]CAGGCGTGAGCCACT	54778
rs145521863	snp	C/T	0.00597247	0.0543191	intron-variant	RNF111	GRCh38.p7	15:59089259	GTTTCCCTAATAGAA[C/T]CAAGCAAAAAAGGCA	54778
rs145561425	snp	G/T	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59056221	ATTTTGAATGACTAA[G/T]ACTGGCTGTTTGAAA	54778
rs145567857	in-del	-/C	0.00557542	0.0525036	intron-variant	RNF111	GRCh38.p7	15:59044037	ACTGTCTTTTTTTTT[-/C]CTGGTGGGGGGAGAC	54778
rs145586691	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59032882	GTGCTCTTGCTCATG[C/T]GTGCTGACTCTCTCT	54778
rs145639332	snp	G/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:58999238	CTGTTAAGCTAGTCA[G/T]TAGAGAGATTTGCAA	54778
rs145643424	snp	C/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59053996	GCTGGAGGGCAGTGG[C/T]GCCATCTTGGCTCAC	54778
rs145695296	snp	C/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59014765	ATTGCAGACTTTTTT[C/T]TTTTTTTTTGAGACA	54778
rs145696454	snp	G/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59075812	TGTTGGTGCTCACTG[G/T]TTCTTCATACTAAGA	54778
rs145710506	snp	A/G/T	9.92452e-05	0.00704375	intron-variant	RNF111	GRCh38.p7	15:59058565	GGTATGTAAAAAAGT[A/G/T]GGGGAGGGGAGACTT	54778
rs145722313	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59045492	CTGCGCCCGGCCTTA[C/G]TTTTTCCTCTTTTTA	54778
rs145733177	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59063664	AGTTTTGGATGCAAG[C/T]CTGTTTGAGAAACAA	54778
rs145754175	snp	A/T	0.0414363	0.137845	intron-variant	RNF111	GRCh38.p7	15:59041478	GAACTGCTTGAACCC[A/T]GGAGGCGGAGGTTGC	54778
rs145756052	snp	C/G	0.00597247	0.0543191	intron-variant	RNF111	GRCh38.p7	15:59008448	GGTCTCGACTCCTGA[C/G]CTCAAGCAATCCTCC	54778
rs145784016	snp	G/T	0.000399281	0.0141238			GRCh38.p7	15:58995857	TTTCCTTTGTCAGTC[G/T]TGGAATGAGCCGTTT	54778
rs145797620	snp	C/T	0.0130921	0.0798413	intron-variant	RNF111	GRCh38.p7	15:59018054	ATGAGGCACCACGCC[C/T]GGCCTATTTGTTGAG	54778
rs145842619	snp	A/C/G	0.000461905	0.0151903	missense	RNF111	GRCh38.p7	15:59031583	TGCTACCTAGTTCTA[A/C/G]TAGTTCCAGTGAGAA	54778
rs145869490	snp	C/G	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59049202	CTCCTCGCTCTGACC[C/G]TGGTTACCACCACTC	54778
rs145870451	snp	C/G	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:59085242	GAAGAGTTTGCTATT[C/G]TAATCGTCCTTAATG	54778
rs145882076	snp	A/G/T	3.30132e-05	0.00406273	missense	RNF111	GRCh38.p7	15:59031514	AGAAACAAAAAGAGA[A/G/T]GATATTAATGCAGAG	54778
rs145894675	snp	C/T	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:59039111	CTGGGATTACAGGCA[C/T]GTGCCACCATACCTG	54778
rs145929398	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59032542	TCCTCCCACGTCAGC[A/G]CCTCAAGTAGCTGGG	54778
rs145948168	snp	C/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59003639	ACTCCTGAGCTCAAG[C/T]GATCTGCCTGCCTCA	54778
rs145948270	snp	C/T	0.0158469	0.0875917	intron-variant	RNF111	GRCh38.p7	15:59035123	TATAAAACCATCAGA[C/T]CTTGTGAGACTTACT	54778
rs146018320	snp	C/T	0.00517822	0.0506191	intron-variant	RNF111	GRCh38.p7	15:59082248	CCATATGACCCAGGC[C/T]AATTTCTTTATGCAA	54778
rs146027904	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58993206	TGTAAATAAAAATGT[G/T]TTAAAATAATTAGTA	54778
rs146049004	in-del	-/T	0.10393	0.202888	intron-variant	RNF111	GRCh38.p7	15:58993369	CAAAAATAAAAAAAA[-/T]ATAACTGTAAATACA	54778
rs146050419	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020871	CTATACTTCAAACTT[C/T]TGTGGGAACAGTTTT	54778
rs146068178	snp	A/G	0.0422008	0.138995	intron-variant	RNF111	GRCh38.p7	15:59023109	AAAAATTAACTGGGC[A/G]TGGTGGTGCGTGTCT	54778
rs146068952	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58991352	TACATTTTAAAGAGC[A/G]GTACTGCATTATTAC	54778
rs146072408	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59086453	AAGATTATACTAATT[C/T]TCTACATCTGATTTA	54778
rs146172859	snp	C/T	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59006889	CCTCCCGGGTTCAAG[C/T]AGTTCTCTGCCTCAG	54778
rs146173490	snp	C/G	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59066197	TGTGCCATAGGAAAA[C/G]ATGATCTATTGCCAT	54778
rs146182652	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59062227	TATGTATTTTTTGTA[A/G]AGATAGGGTTTTGCC	54778
rs146191182	snp	A/T	0.0611083	0.163768	intron-variant	RNF111	GRCh38.p7	15:59009161	GATGGGGTTTCACCA[A/T]GTTGGCCAGGCTGGT	54778
rs146193473	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59069233	GATTGTCCAGACCTG[C/T]CCTATCTCTTGGGAA	54778
rs146289847	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58994172	CCTCCCAGGTAGCTG[A/G]GATTAGAGGTGCACG	54778
rs146293341	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59090974	GTTTCTAAGTATGGA[A/G]GTTTATTTCTTATAC	54778
rs146294214	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59046846	GACTTGTATTCAGGA[C/T]ATATAAGGAACTCTT	54778
rs146297677	snp	C/T	0.00301226	0.0386918	synonymous-codon	RNF111	GRCh38.p7	15:59030993	AGTTGAGATGATTAA[C/T]AGTAAAGTGGGGAAT	54778
rs146308750	snp	A/G	0.00795532	0.062565	intron-variant	RNF111	GRCh38.p7	15:58998031	TGCCTCAGGCTCCCT[A/G]GTAGCTGGGATTACA	54778
rs146313614	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59052016	TACAGGATAAATATC[C/T]ATATAAGATCTTACA	54778
rs146335394	snp	C/T	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59086965	TAGAAGAGGTAAATA[C/T]TGATGAATGCCTGAA	54778
rs146387692	in-del	-/TTTT			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986910	GGGAGGGAATTAATG[-/TTTT]TTTAGTGAACACTTA	54778
rs146390613	snp	C/G	0.00557542	0.0525036	intron-variant	RNF111	GRCh38.p7	15:59006609	ATTTGCTATTTTTTT[C/G]CTTTACATTTCTAGC	54778
rs146416860	snp	C/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59033677	AATATAGTAATTGAA[C/T]GTCATTATCAGTGCC	54778
rs146453973	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59029284	TGTGTTTTATCATTG[C/T]GACTTCTGTGTTCTT	54778
rs146479435	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59063000	TGCCAGATACTGGGG[A/T]CAGCATTGCTTTATG	54778
rs146497795	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59027250	CCTCTGAAATCCACC[A/G]GAACATAACTCTGAC	54778
rs146498097	snp	C/G	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59066414	TTGGGAGTTCAAGAC[C/G]AGCCTGACCAACATG	54778
rs146537565	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF111	GRCh38.p7	15:58988398	GATTTGACAATGGAG[C/T]GATGAAGGTAACCCG	54778
rs146551752	snp	C/T	0.0119091	0.0762411	intron-variant	RNF111	GRCh38.p7	15:59068434	CAACATGGTGAAATC[C/T]CATTTCTACTAAAAT	54778
rs146619508	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59015314	CATGTTTTGTGTTTT[A/G]TATGTTTCTAAATTT	54778
rs146626092	snp	A/G	3.29625e-05	0.00405958	missense	RNF111	GRCh38.p7	15:59066817	ACTGGCCCTCCTGCA[A/G]TGCCAAGGTTACCTT	54778
rs146644404	snp	C/T	8.24763e-05	0.00642116	synonymous-codon	RNF111	GRCh38.p7	15:59085737	CTTGGCCCATTATCA[C/T]GCACCTCCTCGACTT	54778
rs146696553	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59004336	ACTAAAATTCTGAAG[A/G]TTGCAAAAAAGTATA	54778
rs146698486	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59062363	AGACTTTCATATCCA[A/G]TTGCTTCTTGGACAT	54778
rs146720686	snp	A/G	0.0252325	0.109451	downstream-variant-500B	RNF111	GRCh38.p7	15:59097471	CACTTCAGCATTTGA[A/G]CCATAACAGTTGTGA	54778
rs146735071	in-del	-/TC	0.00312255	0.0393894	intron-variant	RNF111	GRCh38.p7	15:59067126	TTCCTGCCCCTCTTG[-/TC]TCTCTCTCTCTCTCC	54778
rs146735876	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59001775	TATTTTTTATGAAAT[C/G]ATGTTTAAAGAACTA	54778
rs146740851	snp	C/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59059818	CTTGCTAACTGCTTA[C/T]CAATAGGGACACTGT	54778
rs146762281	snp	A/G	0.00795532	0.062565	intron-variant	RNF111	GRCh38.p7	15:59094360	TGTTTTTGAGAGAGA[A/G]TTAAATGATGTAATA	54778
rs146786527	in-del	-/TTTAT	0.0456336	0.143994	intron-variant	RNF111	GRCh38.p7	15:59084004	TAATTTATTATAAAA[-/TTTAT]TTTATGACTAATCTA	54778
rs146814439	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58991683	ATAGCAGGGGCGGCA[A/G]ATGCATTAGGTGAGG	54778
rs146819558	snp	A/C	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59044311	GCTGGGTTTACAGGC[A/C]TGAGCCACCACGCCT	54778
rs146842281	snp	C/T	0.0463947	0.145069	intron-variant	RNF111	GRCh38.p7	15:59064460	AGAATGGCGTGAACC[C/T]GGGAGGCAGAGCTTG	54778
rs146857690	snp	C/T	0.00636936	0.0560724	intron-variant	RNF111	GRCh38.p7	15:58989199	TTTTGTAAAAATCTT[C/T]ATGTCAGTATAAGCC	54778
rs146861234	snp	C/G	0.00557542	0.0525036	intron-variant	RNF111	GRCh38.p7	15:59083577	CTAAATACACGTTTC[C/G]TAGGTGTGTTAACTT	54778
rs146900393	snp	A/G	0.00557542	0.0525036	intron-variant	RNF111	GRCh38.p7	15:58992297	TGATTCGCCCGTCTC[A/G]GCCTCCCAAAGTGCT	54778
rs146937638	snp	A/G	0.00795532	0.062565	intron-variant	RNF111	GRCh38.p7	15:59084863	ATGTAAGTAAGAGGC[A/G]TGGACCTTTTTTCCT	54778
rs146990852	snp	C/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59046142	AATCAGATAATCTTT[C/T]ATTATCTCCGTTATT	54778
rs147023567	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59005611	CAAGAGGAATTTGAG[A/G]TTCACTTGAATAAGT	54778
rs147025544	snp	A/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59064046	TAATGAGTAATTACT[A/G]TACATATTATAATTT	54778
rs147039771	snp	C/G	0.0279526	0.114869	intron-variant	RNF111	GRCh38.p7	15:59007700	CTTTTTAGTTTTAGT[C/G]TTATTGGGTGTGTAA	54778
rs147043681	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59067866	ACAGCCTTCTCATTT[A/G]CAGACCTGTAGCATG	54778
rs147137462	in-del	-/GAG	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59076468	TCTAGGCACAGTAAA[-/GAG]GTAAATTTTTAAGAA	54778
rs147164553	snp	C/T	0.00438332	0.0466095	intron-variant	RNF111	GRCh38.p7	15:58990632	GCACTCCAGCTTGGG[C/T]GACAGAGCGAGACTG	54778
rs147166357	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59042494	ATTTTGAATCATAAT[C/T]AGGAATACTTTTACC	54778
rs147184653	snp	C/T	0.00953873	0.0683987	intron-variant	RNF111	GRCh38.p7	15:59078595	AGGCACAGTGGCTCA[C/T]GCCTGTAATCCCAGC	54778
rs147189555	snp	C/T	8.24056e-05	0.00641841	missense	RNF111	GRCh38.p7	15:59076158	GTTGCGCAGCCCCAG[C/T]CCCAGCCCCCTCCAC	54778
rs147200550	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RNF111	GRCh38.p7	15:58987268	CAAATTCACTTTAAC[A/C]GTGAGGTGCCGTGAT	54778
rs147202432	snp	G/T	0.00716266	0.059414	intron-variant	RNF111	GRCh38.p7	15:59039888	TGCCCAGCTAATTTT[G/T]TGTGTTTTAGTAGAG	54778
rs147220877	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59075336	TAAAAGGAAGCAGTG[A/C]TTTAACTTTTTTTAT	54778
rs147271765	snp	A/G	0.0115144	0.0749975	intron-variant	RNF111	GRCh38.p7	15:59028356	CATTCTGAGTCCCCC[A/G]GTGGATGCCTGAAAC	54778
rs147291661	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59061498	CACTCTCCTTTTCCT[C/T]AAGGTTTTCATTCCC	54778
rs147326688	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59058910	GACAGCCTACAGAAT[G/T]GGGGGAAGAAAAATA	54778
rs147376145	snp	C/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59016500	GAACCTGTATTTTCT[C/G]TCTCTGCCCACAGAT	54778
rs147395171	snp	G/T	0.00478085	0.0486577	intron-variant	RNF111	GRCh38.p7	15:59043180	TTTTTTTTGAGACAG[G/T]GTCTCATTTTGTTGC	54778
rs147419165	snp	C/T	9.97921e-05	0.00706301	missense	RNF111	GRCh38.p7	15:59055767	CAGGAGCCACGGAAC[C/T]GCAGTAGGATTTCTA	54778
rs147431267	snp	C/T	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59040079	GTGGTTTTTGCTCTG[C/T]TGGGTTGCCAATGCT	54778
rs147436747	snp	C/T	4.94214e-05	0.00497074	missense	RNF111	GRCh38.p7	15:59076090	GCCATCAGGCCGCTG[C/T]TGCTGCCCCAAGTCA	54778
rs147481319	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59003204	CACTGCAACCTCTGC[C/G]TCCTGGGCTCAAGCG	54778
rs147482410	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59061131	ACGTACATTTTATGT[A/G]ATACAGTCCCAACTT	54778
rs147502614	snp	A/G			utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096235	TCAAGATACTTTCAT[A/G]TACAGGATAGCCTAA	54778
rs147517836	snp	C/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59001171	CGTGACTAGCCATAG[C/T]ATGGTTGACCTGCTT	54778
rs147537273	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59026370	CTAGTATCAGGAGTA[A/G]TTAGCATGCAGTCAT	54778
rs147539166	snp	C/G	0.0115144	0.0749975	intron-variant	RNF111	GRCh38.p7	15:59092970	ACACCACACTGCACT[C/G]CAGCCTGGGCAATAG	54778
rs147556854	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022365	TGTCTAAATGTAAGG[A/G]TGGTTCCATCTTTGC	54778
rs147573238	snp	C/T	0.0130921	0.0798413	intron-variant	RNF111	GRCh38.p7	15:59024055	ATGGTCAGTTTCTCT[C/T]TTTTAAGGACCTGAT	54778
rs147575369	snp	G/T	0.00636936	0.0560724	intron-variant	RNF111	GRCh38.p7	15:59087904	GGTTATTGGTCTTTT[G/T]TGTCAGAATGGTTCA	54778
rs147608103	snp	C/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59037219	TTTTAACTTTATTAG[C/G]GATTTCTATTATGTG	54778
rs147659443	snp	A/G	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59007722	GGTGTGTAATGGTAT[A/G]TTACTATAGTTTTAA	54778
rs147679363	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59071470	GGTGGATCGCTTGAC[C/T]GCAAGAGTTCGAGAC	54778
rs147684297	snp	G/T	8.24504e-05	0.00642016	missense	RNF111	GRCh38.p7	15:59031374	ACGGTCTCATAAGTG[G/T]CCTCGGACTGAGACA	54778
rs147700741	snp	A/G	0.00154453	0.0277467	missense	RNF111	GRCh38.p7	15:59055771	AGCCACGGAACCGCA[A/G]TAGGATTTCTACTGT	54778
rs147710399	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59023868	TTGAAGATTTACTTT[A/G]TAACTTTGAGCCTTG	54778
rs147746074	snp	C/T	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021445	TATGAACCACCATGC[C/T]TGGCCTATGCCCTTC	54778
rs147781918	snp	A/G	0.00835141	0.0640778	intron-variant	RNF111	GRCh38.p7	15:59054465	CAGAGATAATAGACT[A/G]CTCAGTCTCATCATA	54778
rs147821959	snp	A/G	1.64803e-05	0.00287052	missense	RNF111	GRCh38.p7	15:59031324	GTAAGACATTCCCAG[A/G]CCATTTTGAATGCTA	54778
rs147850656	snp	A/G	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59007451	CCGTTGTAGCTGTAT[A/G]ACATAATTTATCCAT	54778
rs147871676	snp	C/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59033704	TGCCAGGGGTTCATA[C/T]AGCCTCAAGTATTAA	54778
rs147886970	snp	C/T	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59037692	AAATACAAAATTAGC[C/T]GAGCGTGGTGGCGCA	54778
rs147958409	snp	A/G	0.00835141	0.0640778	intron-variant	RNF111	GRCh38.p7	15:58995563	TCCCGGGTTCAAGCA[A/G]TTCTCTGCCTCAGCC	54778
rs148014056	snp	G/T	0.0138799	0.0821421	intron-variant	RNF111	GRCh38.p7	15:59039785	GCAGTGGTGCGATAT[G/T]GGCTCAGTACAACCT	54778
rs148030046	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59090039	AGATATATAACTATA[C/T]CATTAAATGTGGTGG	54778
rs148031195	in-del	-/ATC	0.0295035	0.117819	upstream-variant-2KB	RNF111	GRCh38.p7	15:58987314	GCATATGATATGGGT[-/ATC]ATTTGTTGTGAAAGA	54778
rs148044390	snp	C/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:58997040	ATTTCTACTAATATG[C/T]TTAATTTTTACTTAG	54778
rs148046418	snp	C/G	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59050335	CATGTTTTCCAAAAG[C/G]CCTAGAGAACAAATT	54778
rs148083008	snp	C/T	0.0356815	0.128715	intron-variant	RNF111	GRCh38.p7	15:59028046	TGGCCAGGCTGGCCT[C/T]GAACTCCTGACCTCA	54778
rs148099928	snp	A/T	0.00517822	0.0506191	intron-variant	RNF111	GRCh38.p7	15:59000559	TCTACGAAAAATACA[A/T]AACAGCCAGGTATGG	54778
rs148135453	snp	A/G	3.30398e-05	0.00406434	synonymous-codon	RNF111	GRCh38.p7	15:59031476	AAAGAGATTTGTAAA[A/G]AATAATTCCTCACAG	54778
rs148167029	snp	A/C	0.00438332	0.0466095	intron-variant	RNF111	GRCh38.p7	15:58990131	CTATCTTTGCTTGCT[A/C]TACATTAGATCTCCG	54778
rs148194852	snp	C/T	8.23784e-05	0.00641735	missense	RNF111	GRCh38.p7	15:59076057	GCCCTGTTTCTTCCT[C/T]CCGAGCTGCAATCTT	54778
rs148222813	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:58992883	CGTTCATTCATGTTT[A/G]GGCTGGACATGGTGG	54778
rs148226046	snp	G/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59074116	TATTCAGTAAACCAC[G/T]TAAATAGCTGTACTG	54778
rs148259187	snp	C/T	0.000399281	0.0141238	intron-variant, synonymous-codon	RNF111	GRCh38.p7	15:59022569	AATCTCCTCACATGG[C/T]TATCCCTTGTGCAGT	54778
rs148310555	snp	C/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59025336	CCTAGCAGAAATCTC[C/T]TGAGAAATTTTAGTA	54778
rs148328045	in-del	-/CTCC			intron-variant	RNF111	GRCh38.p7	15:59067257	TTTTTTTTTTTTTAA[-/CTCC]CTCCCATTCTTCCTT	54778
rs148345169	snp	A/T	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59006546	AAAAGATGAAAGAAT[A/T]GTACAGTGAACGCCC	54778
rs148348838	snp	A/G	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:59064908	TGAATCTTACCAAGC[A/G]GAGCCTGAAGCACCC	54778
rs148379601	snp	C/T	0.0279526	0.114869	intron-variant	RNF111	GRCh38.p7	15:59016316	CTGGGACTACAGGCA[C/T]GCACCACCACGCCCA	54778
rs148402169	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096816	GCCACTGGAATACCC[C/T]GGGTCTGTGCCAAGG	54778
rs148454699	snp	C/T	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59033088	AAAAGATTAATTTCT[C/T]GTGAAATTAGGGAAT	54778
rs148471640	snp	A/G	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59083034	CACACCTTTAGTCCC[A/G]GCTACTCAGGTGGCT	54778
rs148486063	snp	A/T	0.0197687	0.0974348	intron-variant	RNF111	GRCh38.p7	15:58991052	TGTAATCCCAGCACT[A/T]TGGGAAGCCGAGGCG	54778
rs148490740	snp	A/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59070756	GTTCCTTTTGTTTCT[A/G]TTATTCCCCCTAAAC	54778
rs148521879	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59023584	TGTCTTACTGTTGCC[A/G]GTGGTTTTCTACTAT	54778
rs148524858	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59087287	TATTTAAATGATAAT[A/G]CTATGCTTTGAACAA	54778
rs148537554	snp	C/G	0.00795532	0.062565	intron-variant	RNF111	GRCh38.p7	15:58994180	GTAGCTGGGATTAGA[C/G]GTGCACGCTACCACG	54778
rs148576052	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59026414	TGAAATGATTGGATC[A/G]ATCTACACAAAGAGG	54778
rs148611438	snp	A/G	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59062235	TTTTGTAGAGATAGG[A/G]TTTTGCCATGTTGCC	54778
rs148641641	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59013828	GAGTCTCACTCTGTT[A/G]CCCAGGCTGGAGTAT	54778
rs148662511	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59007317	CTGTCTGGAATTTCA[A/G]ATAAATAGAAGCATA	54778
rs148663219	snp	G/T	0.0592355	0.161582	intron-variant	RNF111	GRCh38.p7	15:59066508	CCAGCTACTCAGGAG[G/T]CTGAGGGAGGAAAAT	54778
rs148684989	snp	A/G	8.23703e-05	0.00641704	missense	RNF111	GRCh38.p7	15:59031210	CCAAGTGATGAAGAT[A/G]ATGATTCCTCTTTTA	54778
rs148696808	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59017160	CCCACCCCCACCCTG[A/G]GTCTGTGGAAAAATT	54778
rs148732193	snp	A/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59053663	TATGTACCACACCTA[A/T]CCTCTGACCGTGCAT	54778
rs148739605	snp	C/T	1.64765e-05	0.00287019	synonymous-codon	RNF111	GRCh38.p7	15:59058408	ATCACAAGCTACTAG[C/T]GCTTCCATTAACAAT	54778
rs148770319	snp	A/G	0.00835141	0.0640778	intron-variant	RNF111	GRCh38.p7	15:59091874	ACCTAGATCCCTCAC[A/G]TGCACAGTTTACAAT	54778
rs148784450	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59001469	CAGTTTAGTGGGGAT[G/T]GGAGGGAGATTTGAA	54778
rs148841886	snp	C/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59025014	GTTTCCTTTTTAAGG[C/G]TGAATACTATTTCAT	54778
rs148843341	snp	C/T	0.00914312	0.0669923	intron-variant	RNF111	GRCh38.p7	15:59089264	CCTAATAGAATCAAG[C/T]AAAAAAGGCATAGGG	54778
rs148858013	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58995966	CATGCATCAGGACAT[C/T]GCTAGGAAACTAAAT	54778
rs148893617	snp	A/G	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59028008	TTTTTTGTATTTTTA[A/G]TAGAGATGGGGTTTC	54778
rs148929654	snp	C/T	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59064026	AGCAAGTAAAGCTAC[C/T]GTAATAATGAGTAAT	54778
rs148964812	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59075859	ACTAATTTAAAGATT[A/G]TGTTTTTTTGGTTAT	54778
rs148964992	in-del	-/TTTG			intron-variant	RNF111	GRCh38.p7	15:59090209	GTTGTGGTTTGTTTT[-/TTTG]TTTGTTTGTTTGTTT	54778
rs148978578	snp	G/T	0.0126979	0.078662	intron-variant	RNF111	GRCh38.p7	15:58989274	ATGGATAAGAAGGAA[G/T]CCCTTTTACTTTTAC	54778
rs149003993	snp	C/T	1.6504e-05	0.00287258	missense	RNF111	GRCh38.p7	15:59031523	AAGAGAGGATATTAA[C/T]GCAGAGGAAGAAACG	54778
rs149013631	snp	A/C	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59018114	CAATCATAATTATTA[A/C]ACTTTTAATGAAGAA	54778
rs149017553	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59081764	GGCTGCAGTGATTCA[C/T]CCCTATAATTCCAAC	54778
rs149051916	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59055032	TAAATTTAGAACAGT[A/G]TAATGCCACACACAT	54778
rs149068814	snp	G/T	0.0023933	0.0345097	intron-variant, utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022445	CTCCCAAAAGATAAC[G/T]TTGACTTCCAGATTC	54778
rs149103549	snp	A/G	0.0103295	0.0711199	intron-variant	RNF111	GRCh38.p7	15:59002232	TCTATTTTCTTGACT[A/G]TCTTCCCGCCATTTC	54778
rs149103756	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59060128	TCCTCCTACCTCAGT[C/T]TCTCAAGTAGCTAGG	54778
rs149135779	snp	C/T	0.00597247	0.0543191	intron-variant	RNF111	GRCh38.p7	15:59011285	TTTCAGTGCATACCT[C/T]TATCATAACACTTAT	54778
rs149141647	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	RNF111	GRCh38.p7	15:59097750	TGGTCATGGGTAGCG[A/G]GTGCCTGTAGTCCCA	54778
rs149172070	snp	G/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59040898	ATTTCGCTTTTTAAA[G/T]TATGTAAAACATTTA	54778
rs149210201	snp	C/T	6.83889e-05	0.0058472	intron-variant	RNF111	GRCh38.p7	15:59084285	AATTTCAAAACAGTG[C/T]TTCACAGCTTGTGGT	54778
rs149223864	snp	C/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:58991929	GATATCAAGGAGTTA[C/T]TGTAACTTTGTTAGG	54778
rs149228057	snp	A/G	0.00835141	0.0640778	intron-variant	RNF111	GRCh38.p7	15:59044880	ATTGTAGATGCCAAA[A/G]TGTTGCCTGTTGTGA	54778
rs149247897	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59039170	GGTTTTTCCATGTTG[A/G]TCATGCTGGTCTCGA	54778
rs149299252	snp	A/G	0.00438332	0.0466095	intron-variant	RNF111	GRCh38.p7	15:58990869	AAAGTCCACAATTAC[A/G]TTTGAATGTCTTATA	54778
rs149335005	snp	C/T	0.00874735	0.0655527	intron-variant	RNF111	GRCh38.p7	15:59019913	GCAGTGAGTCGAGAT[C/T]GTGCCACTGCACTTC	54778
rs149337155	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59082386	AGGAATAAGATCTAA[A/G]GATATCAAAGATTTG	54778
rs149370927	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59057355	TTTGCATATACAAGC[A/G]TTTGGACATACTAGC	54778
rs149387328	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59023128	TGGTGCGTGTCTGTA[A/G]TCCCAGCTACTCGGG	54778
rs149402714	snp	A/G/T	0.00755907	0.0610114	intron-variant	RNF111	GRCh38.p7	15:59008365	TGAGACTGCAAGGAC[A/G/T]CACCACCATGCCTGA	54778
rs149405820	snp	C/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59068543	CTTTAGAGGTGGAGG[C/T]TGTAGTGAGCCAAGA	54778
rs149427061	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59061781	GTACATGCACATGTA[C/T]ACTTGTTTTTGTCTG	54778
rs149458914	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59013259	GTTCCCATATATCGC[A/T]CACTCAGTTACCCTT	54778
rs149481646	snp	C/T	1.64827e-05	0.00287073	missense	RNF111	GRCh38.p7	15:59075988	TGAGCAACAGTGGTA[C/T]CAGAAGTCATGGAAG	54778
rs149495380	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59042439	CCAACATTTTTTTTC[A/G]CAAGTCATATTTATC	54778
rs149530904	snp	C/T	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:59086154	CGACAGAGTCTCACT[C/T]TGTCACCCAGGCTGG	54778
rs149545213	snp	A/G	0.0126979	0.078662	intron-variant	RNF111	GRCh38.p7	15:58993119	AGGTTGCAGTGAGCC[A/G]AGATTGCGCCACTGC	54778
rs149547152	snp	G/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59046413	ACCCAGGCTGGTCTC[G/T]CACTCCTGGGCTCAA	54778
rs149580992	snp	C/T	0.0364509	0.129988	intron-variant	RNF111	GRCh38.p7	15:59026029	GCCACTGTGCCCGGC[C/T]GGCTTTTTTTTTTTC	54778
rs149583828	snp	C/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59091715	CATGCTCAATACCAA[C/T]GGTCCCCAACCTTTT	54778
rs149599682	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58998193	CAGGCATGAGCCACC[A/G]TGTCTGGCCAAGCAC	54778
rs149615001	snp	A/C/T	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:59034844	TACTACATGTTAATA[A/C/T]GATTTGTATGGATGA	54778
rs149776417	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59014712	CAGGAAAACTGCCAT[A/G]AACAAAGAGGTGTAT	54778
rs149777069	snp	A/G	0.0142736	0.0832652	intron-variant	RNF111	GRCh38.p7	15:59075735	AATTGGTTTAACTGT[A/G]AAACCACTACAGTTT	54778
rs149798282	in-del	-/AT	0.046775	0.145601	intron-variant	RNF111	GRCh38.p7	15:59007632	AGCTGCCAGAGAGTC[-/AT]GTGTGGAGTTCCAGT	54778
rs149813353	snp	C/T	0.00874735	0.0655527	intron-variant	RNF111	GRCh38.p7	15:59049061	GTGATTGTGCCCCTA[C/T]ACTCTAGCCTGACCC	54778
rs149828781	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59018051	GGTATGAGGCACCAC[A/G]CCCGGCCTATTTGTT	54778
rs149865879	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59054770	GTTCTCTTCTTAGTG[C/G]TTAAGCACCCACCCC	54778
rs149869910	snp	A/G/T	0.000395569	0.0140583	missense	RNF111	GRCh38.p7	15:59030962	CCATTGGGGCAGCCA[A/G/T]AAGTTTTCCTGCAGG	54778
rs149932578	in-del	-/A	0.0463947	0.145069	intron-variant	RNF111	GRCh38.p7	15:59087752	AGAGGTGGCAGAAAA[-/A]TCTACATGTAAGCAG	54778
rs149935426	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59036686	CATATCGGTGCATCA[A/G]TATTTATTGGCTATT	54778
rs149971651	snp	C/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59079183	ATAAATGGACTCATT[C/G]TGAAACAAAACTTCT	54778
rs149986959	snp	A/G	0.00478085	0.0486577	intron-variant	RNF111	GRCh38.p7	15:59040766	TAAGTATTTTGTTTT[A/G]TATAGTGTCTTTTTG	54778
rs150024858	snp	A/C	0.00636936	0.0560724	intron-variant	RNF111	GRCh38.p7	15:59083726	TTTCAATGTGTCCTG[A/C]TTTAATGTTTATATA	54778
rs150037496	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58991719	TTCTAGAGAATCTAC[A/G]AATGTAAATTAATTA	54778
rs150056647	snp	C/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59028902	CTCATGCTTCAGCCT[C/G]CCAAGTAGCTGGGAT	54778
rs150073625	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021311	GGGTGCCACCATGCC[C/T]GGCTAATTTTTGTAT	54778
rs150076198	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59024242	TGTCACCATATTCTT[A/T]GTTACCTAAGCTAGA	54778
rs150093011	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59016421	GATCTGCCCACTTTG[A/G]CCTAATTATTTATAT	54778
rs150096989	snp	C/G	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59077880	GACATTTTGATAACT[C/G]TGTTTTGGGCTTCTT	54778
rs150131649	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59050515	CTGACACTAGACTCT[A/G]TATCAAAGGGGTTGA	54778
rs150163497	snp	A/G	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59005076	ATGGGCTTGATGTCT[A/G]TCTAGAGGTGTTCTC	54778
rs150164123	snp	C/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59063303	GACTTTCATTTTCAC[C/G]TTTGTATTATCCAGT	54778
rs150187404	snp	C/G	0.000297118	0.0121849	synonymous-codon	RNF111	GRCh38.p7	15:59031422	GTTAATGAAAAGACC[C/G]TGTTTACATGGCAGT	54778
rs150215030	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59007885	TCAGTATTCAAGTTA[C/T]GTATATGTGTTTGTA	54778
rs150220686	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	RNF111	GRCh38.p7	15:59095577	AAGAGTTGAATATTG[A/T]TATCATACATTTAGA	54778
rs150250552	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59038996	TGAGATGGAGTTTCA[C/T]TTTTGTTGCCCAGGC	54778
rs150287673	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59081977	CTGGAGTGCAGTGGT[A/G]CAACCATAGTTCTTT	54778
rs150300673	snp	C/T	0.142272	0.225598	intron-variant	RNF111	GRCh38.p7	15:58990477	AAAATGGTGAAACCC[C/T]ATCTCTACTGAAAAT	54778
rs150305127	snp	G/T	0.00438332	0.0466095	intron-variant	RNF111	GRCh38.p7	15:59042174	CTGTCACCCAGGATG[G/T]AGTGCAGCATATTGC	54778
rs150335715	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58999631	GTCAGCCACTGTGCC[C/T]GGCCTATTACTGCAG	54778
rs150338183	snp	C/T	0.00874735	0.0655527	intron-variant	RNF111	GRCh38.p7	15:59001971	AAATTGTGTGAATGT[C/T]ATCTCTCAAAATATT	54778
rs150341336	snp	C/T	3.29788e-05	0.00406058	synonymous-codon	RNF111	GRCh38.p7	15:59085728	GCATCCTCACTTGGC[C/T]CATTATCACGCACCT	54778
rs150374141	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59030243	TATCAGGAGAATTCA[C/G]ATTCTCATTAGAGAA	54778
rs150374776	snp	C/G	0.0648419	0.167978	downstream-variant-500B	RNF111	GRCh38.p7	15:59097667	GGCAGATCATGAGGT[C/G]AGGAGATCGAGACCA	54778
rs150425992	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59034612	TTAAACTGAAATATT[A/G]ATGAGACTTAGCTCT	54778
rs150464433	snp	G/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59073039	TAGCTGGGTGCAGTG[G/T]CACGCGCCTGTGGTC	54778
rs150505471	snp	A/G/T	3.42209e-05	0.00413637	missense	RNF111	GRCh38.p7	15:59055714	GACACTCCAGATCTC[A/G/T]TTGGAGCCAGGGTTC	54778
rs150535891	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59009989	TAAAATGATTTTGCT[A/G]AATTGTAAGTTAATT	54778
rs150537261	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59069855	TGTGATTTTGTAGAT[A/G]TCTTATGTTTGAGTG	54778
rs150587875	snp	C/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59014348	TATTACAAGTCAGAA[C/T]CTGAGCACTAGGACT	54778
rs150605143	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59000928	CTCTGGTGGGGAAAC[A/G]AAGTTGTAGATGGTC	54778
rs150605301	snp	C/T	0.0111196	0.0737302	intron-variant	RNF111	GRCh38.p7	15:59056789	CAGTCGTTAATGTAA[C/T]AGGGATTAATTAATG	54778
rs150623909	snp	A/T	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59043848	GTTTAGTAGGTATGG[A/T]ACCATGGTGTCATTT	54778
rs150656417	snp	C/G	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:59003417	GCCTTTTTCTTTTTT[C/G]AGACAGAGTCTGGCT	54778
rs150660947	snp	A/G	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59087386	ACTTGAACAATGCAG[A/G]GGTTAGGGGTGTTGA	54778
rs150782136	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59074121	AGTAAACCACGTAAA[G/T]AGCTGTACTGTCATC	54778
rs150813804	snp	C/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59025766	TCGGAATTTTGCTCT[C/T]GTCTCCCAGGCTGGA	54778
rs150833991	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59017289	CAGAGATCGTAAATG[C/T]GTCATTCAGCATATG	54778
rs150836057	snp	A/G	0.00517822	0.0506191	intron-variant	RNF111	GRCh38.p7	15:59078908	GGTAAGGCTACTTAC[A/G]ATTAATCATAAAGCA	54778
rs150844885	in-del	-/CC			intron-variant	RNF111	GRCh38.p7	15:59080113	GCCTTCTTGTGTGCT[-/CC]TTTTTTTTTTTTTTT	54778
rs150869550	snp	C/G	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59028571	CTGGATAGTGAGGGA[C/G]TACCGTACTTCATTT	54778
rs150869872	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59053760	TTTCCTTGTAGGACT[A/G]GAGATCTTGTTTTGG	54778
rs150922298	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59001632	CACTTTAGGAAGACT[A/G]AGTCTATTTTGACAG	54778
rs150925872	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59059174	CCCAACCCAACAGAA[A/G]GACAACCCAATTTTA	54778
rs150944278	snp	C/T	0.00914312	0.0669923	intron-variant	RNF111	GRCh38.p7	15:59045379	CATTTTTAGTAGAGA[C/T]GGGGTTTTACCATGT	54778
rs150961347	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF111	GRCh38.p7	15:59097083	ATATAGGAGCTTATT[A/G]AGCTACTGCCATTAG	54778
rs150976565	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59004755	GCAGTCTCTGGAAGT[C/G]TAGCACTTCCCGTTT	54778
rs151012788	snp	A/T	0.00636936	0.0560724	intron-variant	RNF111	GRCh38.p7	15:59033548	GGTCAGAATGTGCAT[A/T]TACTAGTTTTGGGAG	54778
rs151096883	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:58994809	AAGTAAATTGCTTAC[A/G]TTATGCCCATTACAT	54778
rs151101166	snp	A/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59048731	CAAGAAAAGAAATGG[A/T]GGGTTACTTTTTTAA	54778
rs151103723	snp	C/G/T	0.00159649	0.0282165	intron-variant	RNF111	GRCh38.p7	15:59081797	TTTGGGAGGCTGAGG[C/G/T]GGGAGGATCGCTTGA	54778
rs151136272	snp	A/G	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59026882	AGAGTTAACTGGTGT[A/G]CAAACACACACCACA	54778
rs151137765	snp	C/T	0.000199064	0.0099746	intron-variant	RNF111	GRCh38.p7	15:59093466	TCCACCTACCTCAGC[C/T]TCCCAAAATGCTGGG	54778
rs151152591	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:58999361	GTTTGTTTTTGAGAC[A/G]GAGTCACACTGTCAC	54778
rs151224376	snp	A/G	0.022732	0.10416	synonymous-codon	RNF111	GRCh38.p7	15:59066903	AGGACATCCTCATAC[A/G]AGTTGCTTTCAGCAG	54778
rs151246610	snp	A/G	0.00166314	0.0287889	missense	RNF111	GRCh38.p7	15:59058524	CTACTCTTACAAGCA[A/G]TAGTACCACTGGCAC	54778
rs151274795	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59011881	CACTTGGCATATGTT[C/G]CAACTGAAGATAATG	54778
rs151308359	snp	A/G	0.00874735	0.0655527	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021231	TCTCGGCTCACTGCA[A/G]ACTCCGCCTCGTGAG	54778
rs180762081	snp	C/G	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:59033655	CTGATGTTTATAGGG[C/G]AATGAGAATATAGTA	54778
rs180767045	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59016846	CCTGTCACTTACATT[A/G]CTGCTTGAGTTCTGC	54778
rs180781974	snp	A/C/G	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59080826	ACTTGATAAAGTATT[A/C/G]ATAAAAATAAAATAC	54778
rs180785819	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59065921	GAGGCTGAGGCAGGA[G/T]AATCTGTTGAGCAAA	54778
rs180789117	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59049100	ACACACACAAAAAAG[C/T]ATATTTACATTTGTT	54778
rs180792752	snp	G/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59039207	AACCTCAGGTCATCT[G/T]CCCGCCTTGGCCTCC	54778
rs180821053	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58999103	TGAAAAGGTTATTAA[A/G]TATACTACTCCCTTT	54778
rs180921048	snp	C/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:58990878	AATTACATTTGAATG[C/T]CTTATACCTCTGTTT	54778
rs180955201	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59006601	GATTAACAATTTGCT[A/G]TTTTTTTGCTTTACA	54778
rs180982506	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59022985	GGCGCGGTGGCTTAC[A/G]CCTGTAATCCCAGCA	54778
rs181088404	snp	C/G	0.00478085	0.0486577	intron-variant	RNF111	GRCh38.p7	15:59078277	AGTAAGAATATGTCT[C/G]TCTCTGCTTTTGAAA	54778
rs181122099	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020260	CATAAATATAACAAT[A/G]TATGCATTATATATA	54778
rs181129939	snp	C/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59003833	GCCTAAAACAAGTGC[C/G]TAGCTCATTATAGGC	54778
rs181136498	snp	C/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:58988450	CTAAGTCAGCCCTGA[C/T]GGCTAGGGAGTCGCC	54778
rs181136972	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59070267	CCCTTGATTGTCCTT[C/T]GGGAATAAGAATTGA	54778
rs181154721	snp	A/G	0	0	intron-variant	RNF111	GRCh38.p7	15:59053136	TAATTCAAAACATAT[A/G]TTTTGATTCTTTTTC	54778
rs181161523	snp	A/G	0.00438332	0.0466095	intron-variant	RNF111	GRCh38.p7	15:59036048	AATAAAGACATACCC[A/G]AGACTGGGTAATTTA	54778
rs181181625	snp	C/T	0.00247125	0.0350645	missense	RNF111	GRCh38.p7	15:59085741	GCCCATTATCACGCA[C/T]CTCCTCGACTTCATC	54778
rs181281026	snp	C/T	0.00636936	0.0560724	intron-variant	RNF111	GRCh38.p7	15:59066394	GGCGGGCAGATCACC[C/T]GAGGTTGGGAGTTCA	54778
rs181297761	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59089414	CAGGATCTTAAGACA[A/G]TTTTACTCTTTTCAA	54778
rs181375893	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59081719	CAAGACCCTGTGTCC[C/T]TTAACAACAGTAGAA	54778
rs181380653	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59049617	ATACATTAATTCTTT[C/T]GGCAAGAATTTCGTT	54778
rs181392911	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59023960	TATTTAATATTTCCT[A/C]TTCTCCAAGAAGTAG	54778
rs181405164	snp	A/C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59007005	CTTGGCCAGGCTGGT[A/C/G]TTGAACTCCTGACCT	54778
rs181422556	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58991541	ATGTGATACGGCATG[G/T]ATGGAAGTGGTTTTA	54778
rs181422739	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59073225	TCTGTAATCCCAGCA[C/T]TTTGTTTGAGAGGCT	54778
rs181428865	snp	A/G	0.00438332	0.0466095	intron-variant	RNF111	GRCh38.p7	15:59039872	CAGGCACATGCCACC[A/G]TGCCCAGCTAATTTT	54778
rs181450801	snp	A/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59033921	TTTCTGGACAAGTGA[A/T]TTGCTTTAAACTGGT	54778
rs181525339	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020612	TCTCTTTGATGACTA[A/G]TATTTAAGGATTTCA	54778
rs181529721	snp	A/G	0.00122624	0.0247309	intron-variant, missense	RNF111	GRCh38.p7	15:59004143	CATGTTTTTTCCCTC[A/G]TAGATGGCAGTTCTG	54778
rs181539841	snp	A/T	0.00119737	0.0244387	downstream-variant-500B	RNF111	GRCh38.p7	15:59097773	TAGTCCCAGCTACTC[A/T]GGAGGCTGATGCAGG	54778
rs181541592	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:58988553	GTTGGCTTGTTGGTC[A/G]TTTAAAAAGAAACTG	54778
rs181544510	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59053716	CAATTTTTATGAGCT[A/G]TAAGGACTACTGAAA	54778
rs181545481	snp	C/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59070667	TGTAGATAAATAATA[C/G]AAAAGAAAGGAGCTC	54778
rs181552019	snp	A/G	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59036875	TTATCTGTTGTCCAG[A/G]TTGGAGTGCAGTGGT	54778
rs181552980	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59077402	AATGAGAATTTAAAA[A/G]CTTCCTCGCACAGCT	54778
rs181640976	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59044642	AAAACAATTCGAAGA[A/G]AATCACCCACAGTCC	54778
rs181715548	snp	C/T	0	0	intron-variant	RNF111	GRCh38.p7	15:59060003	CAGGAAGTATTCTCT[C/T]CCCTGGAAAACTGAG	54778
rs181724478	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58998808	AATGAGATTGGTTGT[A/G]TTATTAACAAAATTT	54778
rs181746133	snp	A/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59032907	CTCTCTCTCTCTCTC[A/T]CACACACAGTAAATG	54778
rs181754517	snp	A/G	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59027339	GATGGAGTCTCTGAT[A/G]CCTAGAAATCTTGAT	54778
rs181757306	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59016493	AGGATGGGAACCTGT[A/C]TTTTCTCTCTCTGCC	54778
rs181797833	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59011981	AGTGGCTTAATTTTA[A/G]TGTTCTTTTTTGTTT	54778
rs181809598	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59056617	AAAGAGTTAGAGGCC[A/C]TATACAATCAGCTCT	54778
rs181818855	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59086278	GCACGTGCCACCATG[C/T]CTGGCTAATTTTTGT	54778
rs181828347	snp	C/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59090377	TGGGATTACAGGTGC[C/T]CGCCACCACGCCCGG	54778
rs181834463	snp	C/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59073266	GATCACTTGCGGTCA[C/G]CAGTTCAAGACCAGC	54778
rs181925597	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58991615	TTTGACCTGTGACTT[A/C]AATGACTAGAAAAAA	54778
rs181939389	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59048295	GTATGAATATTGATA[A/C]AACAAATGAATATAT	54778
rs181960531	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59080230	GGTTCAAGCGATTCT[C/T]CTGCCTCAGCCTCCC	54778
rs181972051	snp	C/T	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:59024414	CTTCCTTGGAACTTA[C/T]ATTCTACTGAGACGC	54778
rs182000601	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59035857	CAAAGCCATTCAACA[A/G]GTCTCTAGGAAGTTC	54778
rs182005627	snp	A/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:58995813	CTGTCTTTCTGGCAC[A/T]GCAAGATGTTGCAAG	54778
rs182025894	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59070107	CTTAAACTCCTGGGC[C/T]TAAGTAATCCTCCTG	54778
rs182029732	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59085062	GTGGAAGCAGATTTT[C/T]ATTAGATTAATTTTC	54778
rs182032415	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59027987	CACGCCACCATGCCC[A/G]GATAATTTTTTGTAT	54778
rs182037467	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59052555	GTTTGAGTATGCATA[C/T]ATCAGATTAGTGGAT	54778
rs182040651	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59012194	CGGCTGATTTTTGTA[G/T]TTTTAGTAGAGACAC	54778
rs182066126	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58995243	ACTCTAATGGTTGGA[A/T]AGTGTTTATTTTGTA	54778
rs182118504	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59008409	TTTTTTGTAGAGACA[A/G]GGTCTCACTTTATTG	54778
rs182148395	snp	A/C	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59061009	GCCGTGTTGCCCACA[A/C]TGGCCTCAGTCTCCT	54778
rs182152139	snp	A/G	0.00597247	0.0543191	intron-variant	RNF111	GRCh38.p7	15:58992611	TTGCTTGAGCCCAGG[A/G]GTTTGAGACTAGGCT	54778
rs182221775	snp	A/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59007765	TGGTGACTAAAGATA[A/T]TGAAGATTTTTAAAT	54778
rs182256182	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59040605	TGATTCTTAACAATA[A/T]TAACCATTGCTTATT	54778
rs182256532	snp	A/G	0.00597247	0.0543191	intron-variant	RNF111	GRCh38.p7	15:59067891	AGCATGTTTTCTCAG[A/G]GGCAGATGAGGTTTT	54778
rs182260647	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59051054	TACAGTAATATAAAG[A/T]ATATTAAAGACTTGG	54778
rs182262226	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59065049	TGACCCAGAAGAGAT[G/T]AGCTAGGTACTTTGA	54778
rs182265252	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59034508	AATCCTTCCAGTACT[C/T]TTATGAGATGGATTC	54778
rs182294831	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59083285	GGGCACATTGGCTCA[C/T]GTCTGTAATCCCAGC	54778
rs182312274	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59003166	AGTTTCGCAGGCTGG[A/G]GTGCAGTGGCTCAAT	54778
rs182404986	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59005101	GTTCTCCCAAATTCC[A/G]ACTTTCAGTATGCCT	54778
rs182406478	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59046018	TTCAAATATTTTCAC[A/G]TCTCATAACTCCTAA	54778
rs182414170	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59028117	GCCACCGCGCCTGGC[C/G]AGAAACTCCATGCTT	54778
rs182416145	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59013029	TAGGCGTGAGCCACC[A/G]CGACCGGCCTGGTTC	54778
rs182416213	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59078036	GGAAGACAATATGGC[A/G]TAGTAGAGCACTAGC	54778
rs182433276	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58989519	CACGGGTGCTATATC[A/G]TGTGCAGATCCTTCT	54778
rs182433457	snp	C/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59061243	ACAGTCCTAAATGGG[C/G]CTCTCTTAAGGTCAA	54778
rs182475728	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB	RNF111	GRCh38.p7	15:58985862	TTTAGGGAGACGGAA[A/G]AGGAAAAGGGGAGGG	54778
rs182501756	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59017783	TTTTTTTGAGATGGA[G/T]TTTCGCTCTTGTTGT	54778
rs182504457	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:58988103	AGGGGATCCATTGGA[A/G]GCCGCGCGTGCGCGC	54778
rs182513318	snp	A/T	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:59041081	TACTATTGTTGGGGT[A/T]TACAGAGATACTGTA	54778
rs182530051	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59041916	TCATATGTTTTAAAA[A/G]CTTTAGGTCATTTTC	54778
rs182535304	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59025823	GCAACCGCTGCCTTG[C/T]GGATTCAAGCGATTC	54778
rs182544306	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59008828	TTTAGGGTTTACACT[A/G]TGCATCTTTGTCACA	54778
rs182544740	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59073533	CCTCCGTCAGAAGCA[A/G]CTCATTCAGCTTTTA	54778
rs182549552	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59074044	CTTTTGCCAAGCAGT[A/G]ACATTTTGAAAGGAA	54778
rs182552926	snp	G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59092360	GTCTTAAAAATATAC[G/T]TAATTGATGATAGTC	54778
rs182566527	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59019757	TGAGGTCAGGAATTC[C/G]AGACCGGCCTGGCCA	54778
rs182571677	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59058161	ATTTTTTTAAAATGC[A/G]GTAATATTTTGGTAA	54778
rs182581092	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59045442	GATCTGCCCGTCTTA[A/G]CCTCCCAAAGTGCTG	54778
rs182670925	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59086623	AGGAAAGCTTTCAGA[A/G]AAGCTTTCTGGTACA	54778
rs182684863	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58992699	ATGGCACATGCCTGT[A/G]GTCCCAGCTACTCGG	54778
rs182766589	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59001284	GGTTCATGTTCTTCA[A/G]TTATATGAAATATTT	54778
rs182774815	snp	A/G	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59025165	GCAGGGATTACAGGC[A/G]TGAGCCACTGCGCCC	54778
rs182785250	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59091986	GCCACTCACCTCCTG[C/T]TGTGCAGCCAGGTAC	54778
rs182798222	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58996147	TGAAATGAGAAAAAA[C/T]TGTGTGTGTATGTTT	54778
rs182821394	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59057206	ACATCATGCTGTTCA[A/C]AGTGCACATCTCCTC	54778
rs182847886	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59054278	CTTTGTTTTAGAGTC[A/T]TTTGTGTCAGGATTT	54778
rs182868168	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021593	GCTTTGTTAGGTACT[C/T]TCATTTAACCGTTAC	54778
rs182876659	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59087689	TTGTCTTCACATTGA[A/G]TAAGCTGAAGAGTAG	54778
rs182881994	snp	C/G/T			intron-variant	RNF111	GRCh38.p7	15:59072150	TTTTTGCTGATGGAG[C/G/T]GTCTTGCCTTAATGT	54778
rs182885016	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59054834	AATGCTGACAATAAG[A/G]TTATAAGCAGTTTTA	54778
rs182972663	snp	A/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59071985	TTATGTTTGAAAAAA[A/T]GTACATGCTTCAATT	54778
rs182980057	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59074368	GTTTTGTCGACATGG[A/G]AAATCTGTTATTCAC	54778
rs183008315	snp	C/T	0.00478085	0.0486577	intron-variant	RNF111	GRCh38.p7	15:59094510	TTGGCAGCTCCTGTA[C/T]CAAAACAAAACTGGA	54778
rs183153954	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59038269	CTTTGTCTCAAACTA[C/T]AAATATCATTTTACC	54778
rs183221399	snp	C/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:58999982	AGGGATGGTGCTGAA[C/T]CATTAGAAATTGCCC	54778
rs183260540	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59017512	TTTATAAAAACATCA[A/T]TTGTCTTTAGGTTTG	54778
rs183266681	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59000579	GCCAGGTATGGTGGC[A/G]GGCGCCTATAATCCT	54778
rs183287083	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59050133	GCATTGGCGTGATCT[C/T]GGCTCACTGCAATCT	54778
rs183287415	snp	C/T	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:59034160	CACTATGTATAGTTA[C/T]CTCATTCTTCTTGAC	54778
rs183366410	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59014034	GAGCTTAGGCAATCC[A/G]CCTTCCATGGCCTCC	54778
rs183375887	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59014952	AGACAGAGTTTCACC[A/G]TGTTGTCCAGGCTGG	54778
rs183379608	snp	C/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59053863	CATGACCCATTGTTA[C/T]ATCTCTTATTGTTAT	54778
rs183386736	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58997481	CCAAACTGCATTAGT[A/G]ATCACTATGTTCTTC	54778
rs183404235	snp	G/T	0.0130921	0.0798413	intron-variant	RNF111	GRCh38.p7	15:59047038	ATGTTGCCCAGGCTG[G/T]TCTTGAACTCCTAGG	54778
rs183406253	snp	C/T	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:59071215	AGGCAGGAGAATGGG[C/T]CTGAACCCGGGAGGC	54778
rs183410144	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59046254	GCTGGACTGCAGTGG[C/T]GCCATCAGGGGTCCC	54778
rs183410678	snp	G/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59086492	CAGATTTTGTAAAGT[G/T]CTAAAGGACAAGTTC	54778
rs183410699	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59029445	GCTGATCTTGGATAC[A/G]GCACTGCCTGTGCTT	54778
rs183450764	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59017045	GGGCTCCCACTGATT[C/G]TATATTACGGTGAAT	54778
rs183457862	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59070151	ATTGGCTGGGACTAC[A/G]GGCATGTACCACTGT	54778
rs183460534	snp	A/G	0.0115144	0.0749975	intron-variant	RNF111	GRCh38.p7	15:59085340	AAAAAAGTAAATTCT[A/G]TGTTGTATGCTCCTC	54778
rs183474478	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59052775	TAATAAAATAAAGCT[A/G]TATTGTTGCCCAGAC	54778
rs183556645	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59082810	TTTTGTTTTACTTCT[A/G]TCATTTAAGATTGTA	54778
rs183558737	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59058943	GCAAATCCTTTATCT[A/G]ATAAGCACTTTAGAA	54778
rs183589371	snp	C/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59029102	AATTTTTGAGGATCT[C/G]CTAGACCGCTTCCCA	54778
rs183608286	snp	C/T	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:58996891	AACAGTGGTTTCCTA[C/T]GCAACTCTCCTAATC	54778
rs183617253	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59061936	CTTCCCAGGACTGTG[G/T]TCTCATCCCCCCTTT	54778
rs183733214	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59026152	AGCATCATACCAATA[A/G]TAGTGTATCACAGTT	54778
rs183736878	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59026442	AGGGACTAGTATTAT[A/G]GTTTCAGTATTGAAA	54778
rs183746115	snp	C/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59009711	TGTAATCTCAACACT[C/T]TGAGAAGTTGAGGCA	54778
rs183755215	snp	C/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:58994235	GTAGAGATGGGGTTT[C/T]GCTATGTTGGCCAGG	54778
rs183785137	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59042284	AGTGCACACCCCCAC[A/G]CCTGGCTAATTTTTA	54778
rs183887923	snp	A/G/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59063881	TGAAGGTAATTTAGC[A/G/T]TATCCCAGTGAGTGA	54778
rs183888257	snp	A/G	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59023119	TGGGCATGGTGGTGC[A/G]TGTCTGTAATCCCAG	54778
rs183892298	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59047554	AAAATGCTCAGCACC[A/G]TTAGTTATTTTGTGT	54778
rs183894393	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59006645	ATTTGTTCCTCCAAC[C/T]GTCCATCAACCAAAC	54778
rs183901750	snp	A/G	0.000298309	0.0122092	intron-variant	RNF111	GRCh38.p7	15:59030755	CTTCAATTAAATAGT[A/G]TAATAAAACACATTA	54778
rs183905509	snp	A/G	0.00517822	0.0506191	intron-variant	RNF111	GRCh38.p7	15:59037421	GTTAATTTTAGTAAT[A/G]TATTTCTAGGATCTA	54778
rs183911637	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58991097	TCGGGTTCGAGAGCA[G/T]CCAGGCCAACATGGT	54778
rs183922789	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59063294	AAAGGCCAGGACTTT[A/C]ATTTTCACCTTTGTA	54778
rs183928520	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59079785	GAAATGGTAGGAGCC[A/G]TCTTATTAAGGACTT	54778
rs183939239	snp	C/T	5.07919e-05	0.00503918	intron-variant	RNF111	GRCh38.p7	15:59067104	TGGAATTTGAGTCAG[C/T]CTTTCTTTCCTGCCC	54778
rs183944300	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59009251	GGCGTGAGCCACTGC[A/G/T]CCTGGCCACGTATTT	54778
rs184021277	snp	A/G	0.00993419	0.0697739	upstream-variant-2KB	RNF111	GRCh38.p7	15:58986497	GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC	54778
rs184070141	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020772	ACATCCAGCTACCAA[A/G]CTCCAGTCCTCCATA	54778
rs184080834	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59004489	ACCTTGATCAGTGAC[A/G]TACAGTAAAAATTCA	54778
rs184114576	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59079594	AATGGCTGTTGGTCT[A/G]TATCAGACTTCCAAG	54778
rs184202736	snp	A/G	0.00438332	0.0466095	intron-variant	RNF111	GRCh38.p7	15:59010992	TCCCCTTTTCTCCCT[A/G]ACGGTCATCGTTCTA	54778
rs184207940	snp	G/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:58988962	TCATTTGGTATTTTA[G/T]CTATAATTTTCTTGT	54778
rs184221229	snp	A/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59059852	CCCTGTAGCTTGTGG[A/T]TTGACTAAATCACCA	54778
rs184236692	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59043698	TCTGTTGGAAAGATA[C/G]CAACAGAGGAGTCCC	54778
rs184246370	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59027164	CTCCATTATCAACAT[C/G]AGGACTTAGTAATTA	54778
rs184249998	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	RNF111	GRCh38.p7	15:59097209	CTGCTGCATCTTATA[G/T]GTCAAAATGAACATT	54778
rs184260033	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59077001	TAAAAAAATCTGCAT[C/T]GTGCAGACGCAGCTG	54778
rs184265474	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990217	AGAATAGATAACTTT[C/G]GTTTTCTTTAGGTCC	54778
rs184272463	snp	A/G	0.00279162	0.0372561	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096038	CAAATTATACTGTCA[A/G]CCTACTGTTGCTATG	54778
rs184294127	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59038346	TTTTCCATGTGTAGT[C/T]CATACTGTATTGACT	54778
rs184301770	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022174	CAAGCTTCCTATAAA[A/G]TATTTTGGAAATATT	54778
rs184308001	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59005804	ATCTTTAAAACAACA[A/G]CAATAAAAGCTATCA	54778
rs184331808	snp	A/G	0.00478085	0.0486577	intron-variant	RNF111	GRCh38.p7	15:59075634	ATTTTTAAAGTTTCT[A/G]AGATGTATTTGTTAT	54778
rs184336484	snp	C/G/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59019851	ATAGTCCTAGCTGCT[C/G/T]GGGAGGCTGAGGCAG	54778
rs184339877	snp	G/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59043042	TTGATGTCTAGTTTT[G/T]TATCTTGCAGAGAGC	54778
rs184344975	snp	C/T	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:58988105	GGGATCCATTGGAGG[C/T]CGCGCGTGCGCGCAA	54778
rs184433858	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59035637	TCTCGAATGGTTTGC[C/T]CTTAGAAATTACTTT	54778
rs184442281	snp	C/G	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59019426	AAAAAAATTGGCTTT[C/G]TTCTAATTTGTGACG	54778
rs184453769	snp	C/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59035919	CTCTCCAAACTTTTG[C/T]AACCTCTGCCAGTTA	54778
rs184455984	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59059592	TTTTTTGGTTATGGT[G/T]TGGTCTGTTGGTGTC	54778
rs184463356	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59052078	GAATACAACAAATCC[A/G]TAGAAGAGGAAGTAA	54778
rs184464471	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59068942	TAGTTGGGTCTGTGG[C/T]GCGTGCCTGTAATCC	54778
rs184471883	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59003344	TCCTGAGCTCAAGCC[A/G]TCTGCCCACCTTGAC	54778
rs184483062	snp	C/T	0.00160905	0.0283185	missense	RNF111	GRCh38.p7	15:59055810	CCTTGAGGCAGAATG[C/T]AGCAGAAGTTGTGGA	54778
rs184515760	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59088735	CACAACTAATCAGTG[C/T]ATAACCTTTTTTATG	54778
rs184578709	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58987869	CCGGCTTAGCTGGGC[C/T]GAGTCCAGGCGCTGC	54778
rs184588314	snp	A/C	0.00755907	0.0610114	intron-variant	RNF111	GRCh38.p7	15:59002462	ATGGTAAATACGGGA[A/C]GTACGGTTGAGTAAC	54778
rs184614961	snp	A/G	0.00953873	0.0683987	intron-variant	RNF111	GRCh38.p7	15:59072886	TTTTTTTATTAAAAA[A/G]AAAAAAACAAAACAC	54778
rs184631342	snp	C/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59039262	AGCCACCACTCCCGG[C/T]CTTGATATTCTAATT	54778
rs184635651	snp	G/T	0.00636936	0.0560724	intron-variant	RNF111	GRCh38.p7	15:58997799	CCAGCCTGGCGACAG[G/T]GTGAGACTCCATCTC	54778
rs184753931	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59072601	GACTACAGGTGCCCG[C/T]CACCACGCCTGGCTA	54778
rs184757469	snp	C/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59048316	ATGAATATATTTCAA[C/G]ATAAATACGCTGAGT	54778
rs184772034	snp	G/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59015563	TCTTCCTAAAACTAG[G/T]TTAAACAGAAACCTA	54778
rs184775680	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59001747	AAACATACATTATCA[A/T]GGGATTTTATTTTAT	54778
rs184778743	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59065358	TTCAGAGGATACTTT[C/T]GCAGTTCTTCTGCCA	54778
rs184783161	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59088388	ATGTTTAGGAGGTTG[A/G]GTTATCTGCTGAGTA	54778
rs184814244	snp	C/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59035353	CCCAAAGTCTTAACT[C/T]ATTTCAGTATTTACT	54778
rs184837741	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59068636	TTTTTTGAGATGGAG[C/T]GTCACTCTTGTTGCC	54778
rs184880587	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59045500	GGCCTTAGTTTTTCC[G/T]CTTTTTAAAAACAGG	54778
rs184894410	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59028017	TTTTTAGTAGAGATG[A/G]GGTTTCACCATGTTG	54778
rs184901174	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59012512	GTACGTATTGACTAT[G/T]AATGCATGATTGCTG	54778
rs184912069	snp	C/T	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59051572	CTTAAGGTTAGAATT[C/T]CAAGACAAGCCTGGG	54778
rs184924711	snp	C/T	0.00874735	0.0655527	intron-variant	RNF111	GRCh38.p7	15:58994884	TCTTTTGCGTTATCA[C/T]TGCACCAGTTACAAA	54778
rs184929132	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59018690	TTAATATAAGTTGTT[C/T]TACGAAGAAGAATCC	54778
rs184937393	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59083648	TTGTTTTCTCTTAAA[C/G]TTTCATCCATTAAAA	54778
rs184991286	snp	C/G	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59079972	ATAAGAAAAAGGTGA[C/G]TAATACAATAGGCTA	54778
rs185059789	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58996040	TTTATGAAGTAATCA[C/T]GTAAGACTCAGCAAC	54778
rs185155842	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59048214	AAAACCCAAATGTCC[A/G]TCAGTGGATGAATGG	54778
rs185166700	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59016250	TTTTGGCTCACTGCA[A/G]CCTCCACCTCCTGGA	54778
rs185168212	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59086520	TTCAGCAAAACATAC[A/G]TTGCGTTTGCTGTTT	54778
rs185178342	snp	A/G	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59071414	AAGGCAGTGCATAGT[A/G]GCTTACGCCTGAAAT	54778
rs185229230	snp	C/T	0.000227053	0.0106525	intron-variant	RNF111	GRCh38.p7	15:59081295	CCAACGTATGTTTTA[C/T]GTTTTTAAAAAGAAA	54778
rs185229383	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59041279	AGCTTTTCTTGACCC[C/T]GTGCAGTGGCTCACG	54778
rs185232058	snp	C/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59025422	TGCTAATGAAATTTT[C/G]GCTATTTAGAATATG	54778
rs185237991	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59066185	TAAATCATTTACTGT[A/G]CCATAGGAAAACATG	54778
rs185241124	snp	C/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:58998233	TAATATTCCATGTGA[C/T]AAAATGGGAAGTTTT	54778
rs185242253	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59049128	GTTGTGAAACAGATC[C/T]CCAGAACTTTTCCAT	54778
rs185278199	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59032631	TTGCCAAGTTGCCCA[C/G]GTTGGTCTTGAACTC	54778
rs185296324	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59084696	TCACCATGCTGTGCA[A/G]TAGAATATCAGAACT	54778
rs185368431	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59078616	TAATCCCAGCACTTT[A/C]GGGAGGCCGAGGCGG	54778
rs185383269	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59061355	CCAACCCTCACATTC[A/C]AGCCATCTAGCTTCA	54778
rs185389717	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59046151	ATCTTTCATTATCTC[C/T]GTTATTTACCAGTGT	54778
rs185456803	snp	A/G	0.0225045	0.103662	intron-variant	RNF111	GRCh38.p7	15:58992959	GGATCACCTGAGGTC[A/G]GGAGTTTGAGACCAG	54778
rs185554873	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59028380	CTGAAACCATATAGT[A/G]TTTTTTTTTTCATAT	54778
rs185583969	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59039002	GGAGTTTCACTTTTG[C/T]TGCCCAGGCTGGAGT	54778
rs185595816	snp	C/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59006175	CCAGATTTTATATAG[C/T]GAACTTATTTTAAAA	54778
rs185718976	snp	A/G	0	0	intron-variant	RNF111	GRCh38.p7	15:59022682	ACCTCTTCACACTCC[A/G]TATAAATCATTCTTC	54778
rs185735815	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990476	CAAAATGGTGAAACC[C/T]CATCTCTACTGAAAA	54778
rs185752240	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59055540	GTTTACCGAGTGCCA[A/G]TCATGATTTTTAATT	54778
rs185763750	snp	C/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59080309	TATTTTTAGTGGAGA[C/T]GGGGCTTCGCCATGT	54778
rs185765967	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59003840	ACAAGTGCCTAGCTC[A/C]TTATAGGCTTTCAAT	54778
rs185774302	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:58988528	ACAGACGCGTCAGAT[G/T]TTGTATGGAGTTGGC	54778
rs185785492	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59078116	TTGGTGACTTTGGAT[A/G]AGTTATTTAATCTCT	54778
rs185906803	snp	C/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59056182	AGTACTTTTTAAATA[C/T]AAACACAAAAGCAGT	54778
rs185910482	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59040015	CCACTGCGCCCTGCC[C/G/T]GATTTTCTTTTATTG	54778
rs185915422	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59000435	AGGACCTCAGGACCG[A/G]GCCTGGTGGCTCACA	54778
rs185918018	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59024040	CTGCTGTTCTTTTCT[A/G]TGGTCAGTTTCTCTC	54778
rs185933955	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59061154	CCCAACTTTATTTCA[C/G]AATATTCCAAAAACT	54778
rs185939498	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59073226	CTGTAATCCCAGCAC[C/T]TTGTTTGAGAGGCTG	54778
rs185941850	snp	A/C	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59090011	AAAAATGTATTAAAT[A/C]AATATAAATGTCAGA	54778
rs186078357	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59007050	CTCAGCCTCTTGAAG[C/T]GCTGGAATTCCAGGC	54778
rs186079882	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59033874	AACAGAAATCCAAAA[C/T]GTTGAAACCAAGTAC	54778
rs186138076	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59092056	GTAAAGAATAATCAT[A/G]AAGTGTGAAAATTAC	54778
rs186150167	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59057451	CATTGTATAGAAAGT[C/T]AACCCTCTCATTCCA	54778
rs186195135	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58988675	TACAACAGTTCTTAA[A/T]TAGGTTATAGTAGAT	54778
rs186216678	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020627	ATATTTAAGGATTTC[A/G]GAATACTTTAACAAG	54778
rs186221982	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59016855	TACATTACTGCTTGA[A/G]TTCTGCTTCCTGTCA	54778
rs186225504	snp	C/T	0.000798403	0.0199641	intron-variant, missense	RNF111	GRCh38.p7	15:59004168	GTTCTGGATTAGCAG[C/T]TTTAAGGTCTCAACT	54778
rs186247889	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59070996	AAGCAGTAGGTTTGT[A/G]TTCAAGAATACGAAG	54778
rs186249699	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59053845	AAAAAGACCCACAGT[A/G]TACATGACCCATTGT	54778
rs186256003	snp	C/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59037056	TGCCTAGGCTGGTCT[C/T]GAACTCCTGGGCTTA	54778
rs186282264	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58998940	CTGGGTGAAAGATCT[A/G]TGTAAAGTGCAGTAT	54778
rs186285021	snp	C/T	0.00597247	0.0543191	intron-variant	RNF111	GRCh38.p7	15:59073855	TATGAAATGTATTTC[C/T]TTAATAGTAAGACTT	54778
rs186285494	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59086372	GATCTGCCCACCTTG[A/G]CCTCCCAAAGTGCTG	54778
rs186305387	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59054106	ACACCTGGCTAATTT[G/T]TTTTGTATTTTTAGT	54778
rs186322781	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59032939	GATATTTAAGTAGAA[G/T]AAGTTTATTTGCAGA	54778
rs186339334	snp	G/T	0	0	intron-variant	RNF111	GRCh38.p7	15:59016501	AACCTGTATTTTCTC[G/T]CTCTGCCCACAGATC	54778
rs186428727	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59085973	TAATTTGCATCATAA[C/G]ATGTACTCTTAATGT	54778
rs186460806	snp	G/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59070308	ATTGTGAAGAAGAGG[G/T]TTCTCATTACTGTTT	54778
rs186464903	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59013561	TTGTATCAGGAGTAC[A/G]TGGTGTCAACATGAC	54778
rs186466915	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59036233	CAGCTAATCTTTATA[C/T]TTTTATTAGAGACTG	54778
rs186542725	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59017090	TATTGCAATGCAATG[A/T]TAATAGAAACAAAGT	54778
rs186582011	snp	C/G	0.0138799	0.0821421	intron-variant	RNF111	GRCh38.p7	15:59049779	TTGAGATGGGGTCTC[C/G]CTCCGTCACCCAGGC	54778
rs186604647	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59082208	AGTTTATACCAGGTT[A/G]TTTAGTAAAATCTGA	54778
rs186609026	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58996227	TTTAACTAAGTCATC[A/C]AACATTCTAATCTGA	54778
rs186617102	snp	C/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020372	CAGGCTTCCTTACCA[C/G]AAATATTAGACACTT	54778
rs186631085	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59014968	TGTTGTCCAGGCTGG[G/T]CTTGTCCTGGCCTCA	54778
rs186635832	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58997671	AAAATACAAAATTAG[C/T]AGGGCGTGGTGGCAT	54778
rs186642957	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59063505	TCATGATTGTCTCAT[A/T]TTTAGTGGGCCCTCT	54778
rs186655528	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59053281	CCCTCCAAAATATCA[A/G]CTCCTAACATTGCAT	54778
rs186664250	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59047196	ATAGACATTTCACCA[A/C]AGTGGCTAATAAAAT	54778
rs186665681	snp	A/C	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59029722	TGGTGTCAGAAGTTA[A/C]AATAGTGGTTAACAG	54778
rs186681244	snp	C/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59079619	TCCAAGAACATCTTC[C/T]AATAAAATGAAATTT	54778
rs186711648	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58991573	TGTAGATTGAGTGGT[C/T]AGGGAGGGCCTTTTT	54778
rs186757625	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58992686	TTAGACAGGCATAAT[G/T]GCACATGCCTGTAGT	54778
rs186771738	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59033940	CTTTAAACTGGTTTT[A/T]AAAAAAATAATGATT	54778
rs186793201	snp	A/C/T	3.29453e-05	0.00405854	missense	RNF111	GRCh38.p7	15:59066895	CATGCATTAGGACAT[A/C/T]CTCATACAAGTTGCT	54778
rs186807966	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59008556	AGTTCCTTCCTCATT[A/G]TCTTGGCACTTTTGT	54778
rs186809253	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59068174	GCAGTGAGCTGAGAT[C/G]ACGCCATTGCACTCC	54778
rs186812875	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59083488	GGTTGCAGTGAGCCA[A/C]GATTGCCACTGTACT	54778
rs186881550	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58995291	ACTAATGGACATTCT[C/T]TTATAAGGAAGAGAC	54778
rs186920060	snp	C/T	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59027340	ATGGAGTCTCTGATG[C/T]CTAGAAATCTTGATA	54778
rs186928682	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021821	TTTCCTAGATTTACT[A/G]TAGCTTTTTGGTTAT	54778
rs186949328	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59060388	GGACGCAGATCACTC[A/G]AGGCCAGGAGTTCAA	54778
rs187073408	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59012150	CAGCCTTCTGAGTAG[C/T]TGGGATTACAGGCAT	54778
rs187074083	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:58989612	ATAGAACTGGTTTTT[A/G]AAGAAAGGTATAAAC	54778
rs187081735	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59005300	CTGGGATTACAGGCA[C/T]GAGCCACTGCACCCA	54778
rs187097248	snp	C/T	0.00636936	0.0560724	intron-variant	RNF111	GRCh38.p7	15:59064651	GTTTGTATTTTTCTT[C/T]CGTCCAAGTTCACAG	54778
rs187112352	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59045285	AACCTCTGCCTCCCA[G/T]GTTCAAGTGATTCTC	54778
rs187121542	snp	C/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59073349	TTAGGTGCGTGGTGG[C/T]ATGCACCTGTAATCC	54778
rs187131045	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59079849	CCTTCACCTTAATGT[A/G]GCACAGGAATAATGA	54778
rs187148007	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59077612	AAAATCTAGCTCATT[A/G]GTTTTTAATACCCCC	54778
rs187225889	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59001983	TGTCATCTCTCAAAA[C/T]ATTGTACTCACCTTT	54778
rs187225933	snp	A/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59042036	CATTTTTAGAAGCTT[A/T]TTATATATTAGCAAT	54778
rs187232897	snp	C/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59025887	AGGCATGTGCCACCA[C/T]GCCTGGCTAACTTTG	54778
rs187234263	snp	C/T	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59007989	GCTGTCTCTGAAGAG[C/T]GGAGGTTTTGATTTT	54778
rs187247944	snp	A/G	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59074170	AATAGAGCACAGGCA[A/G]AATAGATTTAGCATA	54778
rs187253149	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59093780	AAGGATAACTTTGTC[A/G]TACCTCTTCAGTTGG	54778
rs187258596	snp	G/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59058243	TGTTATTAGAGAGCT[G/T]GTATTTTTAAAGTTT	54778
rs187264619	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59018693	ATATAAGTTGTTTTA[C/T]GAAGAAGAATCCTAT	54778
rs187300421	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59040629	GCTTATTTGCCTTGT[C/T]GTATATATGCCATAA	54778
rs187367901	snp	C/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59072167	TCTTGCCTTAATGTT[C/G]GTGGCTATGACTGAT	54778
rs187397344	snp	C/G	0	0	intron-variant	RNF111	GRCh38.p7	15:59054928	TTTTTTATCCTGGAG[C/G]CTTAGGACTGCATAT	54778
rs187450768	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59053977	GTCTCCCTCTGTCAC[C/G]CAGGCTGGAGGGCAG	54778
rs187458896	snp	G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58989138	CGCTGGACTTAGCTT[G/T]ATTACAGTAAAGATA	54778
rs187473583	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021381	GTCTCGAACTCCTGA[C/T]CTCAATTCATCCGCC	54778
rs187502970	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59056858	AACTTTTTGTGTTCC[G/T]ATGTGACACCTGCTA	54778
rs187521418	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59038872	GTTGTCATTCTGATC[C/T]TTCCATTATAAAGTT	54778
rs187531924	snp	C/T			intron-variant, utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022396	TTCTCAGTTCCTCTT[C/T]ACCTGTCAGAGGAGA	54778
rs187535290	snp	A/G/T			intron-variant	RNF111	GRCh38.p7	15:59005964	TGGAGATTTAAATCA[A/G/T]TGCATTTTGAGTTGC	54778
rs187565046	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:58992232	GTATTTTTAGTAGAA[A/G]CGGTTTTTCACCATG	54778
rs187570038	snp	A/G	0.0115144	0.0749975	intron-variant	RNF111	GRCh38.p7	15:59024909	TGGGTAATTCATATA[A/G]GTGGAATCATACAAT	54778
rs187688209	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59004728	AGTTGCCCAAATATA[C/T]ATTATAAATATGCAG	54778
rs187721699	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59038144	TTGATGTCTTGGTAA[G/T]TGCTAGAACCATTTT	54778
rs187735329	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59001618	TTGGCGAATAGGTTC[A/C]CTTTAGGAAGACTAA	54778
rs187771827	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59034734	ATAAAATGATTTGGC[A/G]AAAAGTCTTAGCTAA	54778
rs187803728	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59050671	ATGTGTTTGGAAAGA[C/G]CTATAACACCTGTAA	54778
rs187805868	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59067402	GGCTGGAAAACCCAG[A/C]ATGAGGGAGTAACTA	54778
rs187819783	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59034238	CAGCTTTTGTCAGTG[A/G]ATATTTGCTGCATTG	54778
rs187833973	snp	G/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59082890	TAGAAAATTGCCAGT[G/T]TAACAGTCTTATCTT	54778
rs187893878	snp	C/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59038295	TTACCTTATATTAGG[C/T]TTTAAAAAATTATCT	54778
rs187928530	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59072008	CTTCAATTTAAAAAT[A/G]CTTCAGTTTAAAAAT	54778
rs187973275	snp	A/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59017565	GAACTCTTCAGTTCC[A/T]ATCTCCAAGGAAATC	54778
rs187981173	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59000657	GATGTTTCAGTGAGC[C/T]AAGATGGCACCACTC	54778
rs188003425	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58998967	GTATCGAGCAGTTGT[G/T]TTTTCACTGATAGTA	54778
rs188040594	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59033290	TTCTTTTCCAAGAAT[C/G]TCTTTCCTTTTTCAT	54778
rs188044589	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59016702	TCTCCAAAGAGTTCT[A/G]TATAGCAGGGTTCCC	54778
rs188048283	snp	C/G	0.0174175	0.0916809	upstream-variant-2KB	RNF111	GRCh38.p7	15:58986342	CCTGTGTCAGCCTCC[C/G]GAGTAGCTGGGGTTA	54778
rs188052206	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59051531	CTATAATCCCAGCAC[G/T]TTGGGAGGCTGAGGG	54778
rs188062002	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59017978	TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA	54778
rs188188553	snp	A/C/G	6.62069e-05	0.00575323	intron-variant	RNF111	GRCh38.p7	15:59085625	TAAAAAAGAGACCCT[A/C/G]AGGAGGATTAAACTG	54778
rs188192243	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59086716	ATGTAGCAAATAGCA[C/T]AAGCACTGGGAACTC	54778
rs188208129	snp	C/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59054521	AATGGTGGTATCTTT[C/T]CTCATACAAAACCAT	54778
rs188223395	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58992788	TTGTGCCACTGCATT[C/G]CAGCCTCGGTGACAA	54778
rs188257457	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59084527	TATTTGGAGGTACAG[C/T]ATAGTATTTCAATAC	54778
rs188296440	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59059729	GATATCTCTGGCTCT[C/G]TCTTATATCCTTTGT	54778
rs188298209	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59043367	TCACCATGTTGGCCA[G/T]ACTGGTCTTGAACTC	54778
rs188457456	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59026756	ATGATACAATACAGC[A/G]ATGGATTTTAGAAAA	54778
rs188463432	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59010344	TTCATATTTTTGCAG[C/G]TGTGTCTGTCTTGAT	54778
rs188472528	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58994245	GGTTTCGCTATGTTG[A/G]CCAGGCTGGTCTCGA	54778
rs188507624	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59008948	TGTTAATATTGTCAC[A/G]TATTTTATTTTATTT	54778
rs188520057	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59035419	GGCAAGTCCCTTCTG[C/T]ATATGAGCCTGTAAA	54778
rs188531933	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59029110	AGGATCTGCTAGACC[A/G]CTTCCCAAAGTAGCT	54778
rs188546238	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58997238	TCTCTTTCCTCCTGT[A/G]TTTTATATGTGCATC	54778
rs188559667	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59062822	TGCCAAGATTTCTCA[A/G]CCTTGGCACTACTAT	54778
rs188562531	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59068702	AGCTACCACTTTTCT[A/G]TGTCACCCGACCTTT	54778
rs188582815	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58991266	CTGCACTCCAGCCTG[A/G]GTGACAGAGCAAGAC	54778
rs188604422	snp	G/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59023956	TTCCTATTTAATATT[G/T]CCTATTCTCCAAGAA	54778
rs188615435	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59006708	AATAAAAAAAATAAA[A/G]TTACAGACGCCAGTG	54778
rs188638210	snp	A/G	0.000117508	0.00766421	missense	RNF111	GRCh38.p7	15:59055833	GTTGTGGACCTTACC[A/G]TTGATGAAGATGGTA	54778
rs188650329	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59039278	CTTGATATTCTAATT[C/T]TATCATTTTGCTTAG	54778
rs188691460	snp	C/T	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59009548	CAGATCAGAAAACTT[C/T]GATATTTGAGTCTGA	54778
rs188709998	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59074566	TCCTTGCCTCCCTCA[G/T]CCTTCATAGAATTGA	54778
rs188724305	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59042374	TCAAGTGATCCACCC[A/G]CTCGGCCTCACAAGG	54778
rs188755309	snp	A/G			upstream-variant-2KB	RNF111	GRCh38.p7	15:58987582	AGAAACGGGAATCGA[A/G]CAAGCGCAGAAACAA	54778
rs188779435	snp	C/T	0.00119737	0.0244387	downstream-variant-500B	RNF111	GRCh38.p7	15:59097512	ATTTGAAACGTTTTT[C/T]TTACTCTGGTGACTT	54778
rs188787731	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59077308	TGAGTAAGTTCATTC[C/T]TTTCAAAATGTCCTA	54778
rs188817814	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59014121	GGAGTAGAATTAATA[C/G]TACATTATTTATTTT	54778
rs188841566	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59079201	AAACAAAACTTCTTG[C/G]TTTGTAATATTTGTG	54778
rs188852052	snp	A/G	0.0115144	0.0749975	intron-variant	RNF111	GRCh38.p7	15:58990218	GAATAGATAACTTTC[A/G]TTTTCTTTAGGTCCC	54778
rs188854227	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59046689	TTCTTAAATATGTCA[C/G]CAAAATCACAATCCA	54778
rs188950704	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59059896	CATCTTATATTTTCT[A/G]TCCCTTTTTGCTTTT	54778
rs188956742	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59044158	GCCTCAGCCTCATGA[A/G]TAGCTGGGATTAGAG	54778
rs188959739	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59026279	CAACCCTAATTTTTA[C/G]TTTTGAAAGTTAGTA	54778
rs188977548	snp	A/G	0.00295358	0.0383154	intron-variant	RNF111	GRCh38.p7	15:58993368	ACAAAAATAAAAAAA[A/G]TATAACTGTAAATAC	54778
rs188997941	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59058999	AACTGCCCAACAGGC[C/T]GGGTGTGATGGCTCA	54778
rs188999409	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58990640	GCTTGGGCGACAGAG[C/T]GAGACTGTTTCTCAA	54778
rs189017652	snp	C/G/T	0.000724616	0.0190216	utr-variant-3-prime	RNF111	GRCh38.p7	15:59094911	GTTGACACCATGTTT[C/G/T]AGAACTCTTGCCCTC	54778
rs189032123	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59022684	CTCTTCACACTCCAT[A/G]TAAATCATTCTTCCA	54778
rs189064869	snp	A/G/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59055625	GGCTTATGGGTTTTT[A/G/T]TGGTGACTAAAAATT	54778
rs189097706	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59056337	GCTTACAGCTGTACC[C/T]AAGTAACTGAGGAAA	54778
rs189113680	snp	A/C	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:58998636	CTTGGATATTTGTAC[A/C]TATTTTCTCAAAAAT	54778
rs189116495	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59040028	CCCGATTTTCTTTTA[C/T]TGGGAGGTGATAGAG	54778
rs189136161	snp	A/G/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59073261	AGGCAGATCACTTGC[A/G/T]GTCAGCAGTTCAAGA	54778
rs189142077	snp	C/G	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:59090296	GTGCAGTTGCACAAT[C/G]TCAGCTCACTGCAAC	54778
rs189177862	snp	C/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59036018	TTTACTGTATTAGTT[C/T]ATTCTCATGTTGCTA	54778
rs189199512	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59070183	CCTAGTAGTTTAATT[A/T]GTGTGATGCATCATT	54778
rs189215505	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096567	GACTACTTGCCCTTT[C/T]CTTCATATTAGTAAA	54778
rs189254064	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59035740	AGTCTCTTTGCATAG[C/T]AAGAGTGGCCCATTT	54778
rs189259547	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58995640	TTTTTGTATTTTTAG[C/T]AGAGACGGGGTTTCA	54778
rs189265626	snp	A/C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59019484	AGAAATGAGGTCTCT[A/C/T]GCTCTTTACTAGGAT	54778
rs189274843	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59003002	TCTTCCTTTTTTGTG[A/G]TAAGATCTCATTATG	54778
rs189285127	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59084708	GCAGTAGAATATCAG[A/C]ACTTACTCCTCCCAG	54778
rs189295374	snp	C/T	0.00755907	0.0610114	intron-variant	RNF111	GRCh38.p7	15:59070101	GCTGGCCTTAAACTC[C/T]TGGGCTTAAGTAATC	54778
rs189295551	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59052150	TACTGTGTGTGTTTT[C/T]TGTTCCTTGTGTATT	54778
rs189323946	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59006227	TGTATAATTTATATA[C/G]AATATGAGGCACACG	54778
rs189332943	snp	G/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59072648	TAGTAGAGACGGGGT[G/T]TCACCGTGATAGCCA	54778
rs189352862	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59039058	CAACCTCTGCCTCCC[A/G]TGTTCAAGTGATTCT	54778
rs189423648	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59080813	GCTTGAATACTTTAC[A/T]TGATAAAGTATTCAT	54778
rs189437436	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59065711	AGAGTCCAAAGGAAG[C/G]AAAAAAGATAATGGC	54778
rs189441757	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59048625	AAAATTCTTAATTAC[A/T]GACATTATTTGTAAA	54778
rs189468000	snp	A/G	0.00874735	0.0655527	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020226	CTATATACAATAAAG[A/G]TAATATGTATATACT	54778
rs189471346	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59016043	TTTAGTAGAGACAGG[A/G]TTTTGCCATGTTTTG	54778
rs189493457	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59052915	GTGTTTTATAAAATT[G/T]TGTTTTTTAATGATA	54778
rs189499243	snp	A/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59076604	ATGGCTCACTCCTGT[A/T]ATCCCAGCACTTTGG	54778
rs189529496	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59072932	CTGGCTCATGCATTT[G/T]CTCCCAACACTTTGT	54778
rs189629220	snp	C/G	0.00318978	0.0398085	intron-variant, utr-variant-5-prime	RNF111	GRCh38.p7	15:58988271	CAAGGCATTCGTCTA[C/G]CGACACACCCACAGC	54778
rs189716460	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:58996105	TTTTCAAATACATAA[C/T]GAGTTATGTTCTTAA	54778
rs189729660	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59086019	AGTGTGGGGTTTTTT[A/G]TATACCAAGATACTC	54778
rs189743627	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59045916	TGCTACTGTTTTGTT[A/G]TTTTTCTGCCTGTAA	54778
rs189748460	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59028066	TCCTGACCTCAGGTG[A/G]TCTGCCCGCCTCGGC	54778
rs189756976	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58997932	TTTTTTGAAGCTGAG[A/T]CTCACTCCGTTGCCC	54778
rs189758713	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59013019	GCTGAGATTATAGGC[A/G]TGAGCCACCGCGACC	54778
rs189765845	snp	A/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59078125	TTGGATAAGTTATTT[A/T]ATCTCTCTGTCCTTA	54778
rs189773980	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59061163	ATTTCAGAATATTCC[A/C]AAAACTTTTATATAT	54778
rs189785760	snp	A/G	0.000461414	0.015182	missense	RNF111	GRCh38.p7	15:59031082	AGCAAGAACAAGAAA[A/G]AAGTCTCGTTGTGAG	54778
rs189841802	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59088935	GTGCCATTTTAAACA[A/T]CACAATCACCAACAA	54778
rs189854222	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58994987	AGCATTTATCCCTTT[A/G]CAGCATTTTCCTCAT	54778
rs189886072	snp	C/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59027289	CTGGAAGAACCCCAG[C/T]TGTTTCCAACATACA	54778
rs189916012	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59073979	TTGGTGACTATGTGC[A/C]TTGTCAAGAAACAGC	54778
rs189934079	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59058137	TTGGAATAAGCATAT[C/T]GGTGTTGGATTTTTT	54778
rs190003309	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59032894	ATGCGTGCTGACTCT[C/T]TCTCTCTCTCTCACA	54778
rs190034656	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59065010	TTTATTTGTAAACAA[A/G]CAGAAGATTCCTAAT	54778
rs190081557	snp	C/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59041684	AGGATAAATGCATAT[C/G]TTATTTTGTAAAATA	54778
rs190089576	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59081338	TTTTCTTCTACTTCC[A/T]TTGGTCTTTACAACT	54778
rs190095748	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59025794	GGAGTGCAATGGCGC[A/G]ATCTCGGCTCACCGC	54778
rs190097365	snp	G/T	0.0115144	0.0749975	intron-variant	RNF111	GRCh38.p7	15:59011949	GGGACCAAAGATTCC[G/T]AGCTTATATAAGAAT	54778
rs190098932	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:58992687	TAGACAGGCATAATG[G/T]CACATGCCTGTAGTC	54778
rs190103054	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59008566	TCATTATCTTGGCAC[G/T]TTTGTTGGAAAATCA	54778
rs190239986	snp	A/G	0.00597247	0.0543191	intron-variant	RNF111	GRCh38.p7	15:59078838	CACTCCAGCCTGGGC[A/G]ATAGAGCGAGTCTCC	54778
rs190240776	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59048278	ACTCAGCAATAAAAA[A/C]AGTATGAATATTGAT	54778
rs190245864	snp	A/T	0.0126979	0.078662	intron-variant	RNF111	GRCh38.p7	15:59061875	CATAATGAATAAACA[A/T]GATCTTTTAAAATCT	54778
rs190263383	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59016255	GCTCACTGCAACCTC[C/T]ACCTCCTGGATTCAA	54778
rs190268506	snp	C/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59080167	ACTCTGTCGCCCAGG[C/T]TGGGGTGCAGTGGCA	54778
rs190328756	snp	C/G/T			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:58988081	AAGGTGAGGGGAACG[C/G/T]GGGGGGAGGGGATCC	54778
rs190345785	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59045316	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	54778
rs190359253	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59012178	CATGCATCTCCACAC[C/T]CGGCTGATTTTTGTA	54778
rs190369456	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59036301	GGCCTCAAGAGATCC[A/G]CTGCCCACCTCAGCC	54778
rs190381976	snp	C/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59077684	CATTAAAGTTGTTTA[C/T]GGTTGAGTTTATGTA	54778
rs190491354	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:58988533	CGCGTCAGATTTTGT[A/G]TGGAGTTGGCTTGTT	54778
rs190504424	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59088667	CAGTTATGATCTATA[C/T]AGTTGCTGCAAACAC	54778
rs190517776	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020490	TACACCCTTCATTTT[A/G]CTATTGGCTGTAATA	54778
rs190527865	snp	A/G	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:59003856	TTATAGGCTTTCAAT[A/G]AATATTTATTGAATG	54778
rs190605624	snp	A/G	0.0275645	0.114116	intron-variant	RNF111	GRCh38.p7	15:59027895	CAGTGGTGTGATCTC[A/G]GCTCACTACAACCTC	54778
rs190632819	snp	A/G	0.0123036	0.0774623	intron-variant	RNF111	GRCh38.p7	15:59060586	GCTACAGTGATCCTC[A/G]AGGGCACCACTACAC	54778
rs190647654	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58992271	GCTGGTCTTGAACTC[A/G]TGATCTCAGGTGATT	54778
rs190670604	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59017118	AGTGCACAATAAATG[G/T]ACTCGGATCATCTCA	54778
rs190679237	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59000486	GGAGGCCGAGGCAGG[C/T]GGATCACCTGAGGTC	54778
rs190685573	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59024156	TTTTCAAGAAATCTT[A/T]GGTATTATTTTCCTA	54778
rs190706791	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59034120	AAGGGCTATTCAAGG[A/G]TAAATAATGTGGCTC	54778
rs190808318	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59004891	TTAGAATCTGACAGC[A/G]TAGTAAGATGCTCAC	54778
rs190838328	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59038177	AAGTCATCACAATTT[C/T]TGAGAGCATAGGATC	54778
rs190853421	snp	G/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59071159	AAAAAGTAGCCGGGC[G/T]TGGTGGTGGGTGCCT	54778
rs190855370	snp	A/C	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59086417	AGCCAGGGCACCCAG[A/C]CTGATTTTCTAATCT	54778
rs190866827	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59071764	TCTACCCTCTGGTTT[A/C]TTTCCCAACTTAGTT	54778
rs190913329	snp	C/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59008038	AATTTTTTTAAGAAA[C/T]GGTAGTACTTTCTGT	54778
rs190987334	snp	A/G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020751	ATTAGAATTTAGGGG[A/G/T]CTGAAACATCCAGCT	54778
rs191021292	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59053849	AGACCCACAGTGTAC[A/G]TGACCCATTGTTATA	54778
rs191025352	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59037403	CTAGGTTTGAGAATA[G/T]GTGTTAATTTTAGTA	54778
rs191041586	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58989240	ACCCTAGTCTGGTTA[C/T]ATTTGTGAGGTGAAA	54778
rs191081004	snp	C/T	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59054165	GCTGGTCTCGAACTC[C/T]TGACCTTGTGATCCA	54778
rs191099222	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021563	TAATTAATAATAACA[A/G]CCACTATGCCATGTG	54778
rs191109679	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59086530	CATACATTGCGTTTG[C/T]TGTTTGTATTACATA	54778
rs191133682	snp	A/G	0.00755907	0.0610114	intron-variant	RNF111	GRCh38.p7	15:59017572	TCAGTTCCAATCTCC[A/G]AGGAAATCTGGAAGC	54778
rs191146011	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59016874	TGCTTCCTGTCAGAT[C/T]AGCAGCGGCATTCTT	54778
rs191167162	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59067648	TAATCAAAACTGATA[C/T]TTAATCTAAAAATCA	54778
rs191167342	snp	C/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59050821	AAAGTTTTAAACATA[C/T]AATACGTTATTGCTA	54778
rs191180314	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59034486	TATTTTATGTGTATT[A/C]TCATTGAATCCTTCC	54778
rs191180762	snp	A/G	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59049281	GGAATCACAGTTTTT[A/G]TCTTTTTATGACTGG	54778
rs191204924	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59082993	AATTAGACTATAAAA[A/G]TGAATCTTAGCTGGG	54778
rs191237952	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59092213	ACTAATAAAAAAAAC[C/T]TATTTATGCTCATGG	54778
rs191287545	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59028848	GTAGCGGTGCAGTCC[C/T]AGCTCACTGTAACCT	54778
rs191301384	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59053578	GGAAGTGAGCATTCT[A/G]TAACATATACTTGTT	54778
rs191307384	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58996823	TTAAATTTTCAACCA[A/G]TTAATATCTGTACAC	54778
rs191341411	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59079766	CATAAAGATGTAGAA[G/T]GAAGAAATGGTAGGA	54778
rs191372892	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59033890	GTTGAAACCAAGTAC[A/G]TTCAATGTTTTCTGG	54778
rs191393934	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58999635	GCCACTGTGCCCGGC[C/T]TATTACTGCAGTTTT	54778
rs191404809	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59066206	GGAAAACATGATCTA[G/T]TGCCATACTTACACA	54778
rs191481426	snp	C/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59015512	AGTCTTTCTGACTTT[C/T]CCTCTAGCCTGTTCC	54778
rs191489990	snp	C/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:58997777	GCCAAGATTGCGCCA[C/T]TGCACTCCAGCCTGG	54778
rs191503875	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59063694	AAGAGGTTCTGGACT[A/T]TATATATTCAAAATG	54778
rs191517816	snp	C/T	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:59047377	GCAGGTACCTGTAGT[C/T]GCAGCTACTGGGGTG	54778
rs191525872	snp	A/G	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:59030521	GTTGCTGAAGGTAGT[A/G]AGATATGCAATAAGA	54778
rs191531884	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59070602	AATAGAAGAACAGAC[A/G]TATACTTGATTGTAC	54778
rs191536200	snp	A/C	0.00597247	0.0543191	intron-variant	RNF111	GRCh38.p7	15:59013902	CAAGTAATTCTTATG[A/C]CTCAGCGTCCCGAGT	54778
rs191566962	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59046228	AGACAGGATTTCATT[C/G]TGTTGCCCAGGCTGG	54778
rs191586333	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59007148	TTTTGCCAAATGCAT[C/G]TATTTATTGCCCAAA	54778
rs191619729	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59010352	TTTGCAGCTGTGTCT[C/G]TCTTGATAGATGACA	54778
rs191627824	snp	A/T	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:58994416	AACTCTTGAATACTC[A/T]TTATTCAGATTCACC	54778
rs191633171	snp	C/T	3.31697e-05	0.00407231	synonymous-codon	RNF111	GRCh38.p7	15:59067071	TAGTTCTGGTACCAG[C/T]TATCATGAACAGGTA	54778
rs191643125	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59059830	TTACCAATAGGGACA[C/T]TGTAGACCCTGTAGC	54778
rs191647623	snp	C/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59043427	CTTGCAAAGTGCTGG[C/G]CTTGCAGGTGTGAGC	54778
rs191650809	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59027017	ATTGTTTTGGCTTTG[A/G]GACATGAAATGATGG	54778
rs191665482	snp	C/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59076744	AAAGAAATTGAAATT[C/T]GTTAGATATCACAAG	54778
rs191668810	snp	G/T	0.00478085	0.0486577	utr-variant-3-prime	RNF111	GRCh38.p7	15:59096988	TTTATAATTGCTACT[G/T]ATTTTTTTAATGTAG	54778
rs191793594	snp	C/G	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59079334	TTTTTATGATTAAGA[C/G]CTAGCTACTGAGCTT	54778
rs191823057	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59038314	AAAAAATTATCTAAT[A/G]GCTGTATATATATAT	54778
rs191830530	snp	G/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:58989883	TTCCTTCTTTTTTTT[G/T]TTGTTATAGTTTAAA	54778
rs191832031	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021895	GAGTCAGAGTTTGCT[C/T]TGTCACCCAGGCTGA	54778
rs191836413	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59005634	GAATAAGTTAGACTA[A/G]TTTGAGGTGGGTGTA	54778
rs191856902	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59054788	AAGCACCCACCCCCA[A/G]TGACCTTTTATATTA	54778
rs191910329	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58991613	AATTTGACCTGTGAC[G/T]TCAATGACTAGAAAA	54778
rs191943217	snp	C/T	0.00835141	0.0640778	intron-variant	RNF111	GRCh38.p7	15:59049888	CTGGGATTACAGGTG[C/T]GTGCCACCACACCCG	54778
rs191949197	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59079914	AATGTTTACACCCTA[C/T]TATGACAGAGCTTCC	54778
rs191950345	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58988707	GATCTTTACAGATGG[G/T]TATTTCTCAACCTAA	54778
rs191969817	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59082721	AGAGCTGAAAAAATT[A/T]CCCGTTTTACCCTTC	54778
rs192004007	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59094199	ATATAACAATTATTC[C/T]GTGAAAAAAGTATTA	54778
rs192055744	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59025134	TTACGATCCGCCCTC[C/T]TCCGCCTCCCAAAGT	54778
rs192063165	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59091971	GATGCTCGCTCACCT[A/G]CCACTCACCTCCTGC	54778
rs192097301	snp	A/C	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59062834	TCAACCTTGGCACTA[A/C]TATTGACTTTGGGCC	54778
rs192147011	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59002031	TGATGATAAAATGGC[A/G]AAATGAGGTTAATGA	54778
rs192171526	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59074345	ATGACATCTTCCAAT[A/G]TTAGGCTGTTTTGTC	54778
rs192177322	snp	A/C	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59051885	AGAATATATCACCTA[A/C]ATGAAAACAACCTTG	54778
rs192177713	snp	G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59035424	GTCCCTTCTGCATAT[G/T]AGCCTGTAAAATTAG	54778
rs192188341	snp	C/T	0.00358779	0.0422022	utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58987784	GGTGTTCGGTTTGCG[C/T]AGCGTAGAAACGCCC	54778
rs192190478	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59019316	ATATTACTTTGAATG[G/T]ATCCTTAGGTGTATA	54778
rs192233361	snp	G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59072765	CCTGTCATTTCCATC[G/T]TTTTCCTAGTATCTT	54778
rs192248844	snp	C/T	0.00874735	0.0655527	intron-variant	RNF111	GRCh38.p7	15:59004416	GGATTAAGGTTACTA[C/T]TTTTATCTAGAATAT	54778
rs192305130	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59038949	TTGCCCAGATTCATT[A/G]TATTAGGGGTGCAAA	54778
rs192328103	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59072520	GTGCAGTGGCGTGAT[C/G]TCGGCTCACTGAAAG	54778
rs192332933	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59088250	GATAAGGATTGAGTT[C/T]GAATAGGAGAAAAGC	54778
rs192337700	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59055118	CTAGCTCACGCAAGT[A/G]ATATTTCTTAGGGCT	54778
rs192409271	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59040846	AGGTTCATTTATTTC[A/T]GGGTTGGCTTTTTTA	54778
rs192454020	snp	A/C	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59073511	TAAATAAACTACTTT[A/C]TTTGCTCCTCCGTCA	54778
rs192507864	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59014216	TGACATGCCCCTATT[C/G]TTTTGTGTGTTTCTT	54778
rs192514276	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58997466	AAATCAAGACAGTGG[C/G]CAAACTGCATTAGTA	54778
rs192524469	snp	C/G	0.00716266	0.059414	intron-variant	RNF111	GRCh38.p7	15:59051539	CCAGCACTTTGGGAG[C/G]CTGAGGGAGCCAGAT	54778
rs192547180	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59018563	TTAGAAAAAAAACAA[A/G]CTATATATACAGAAA	54778
rs192566966	snp	A/C	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59083569	GAATCAAGCTAAATA[A/C]ACGTTTCCTAGGTGT	54778
rs192603373	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59000673	AAGATGGCACCACTC[C/T]GCTCCATCCTGGGTG	54778
rs192622257	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59009582	AAGGTGATTAGATAA[C/T]ATAGAACGATACCAA	54778
rs192630343	snp	A/T	0.00478085	0.0486577	intron-variant	RNF111	GRCh38.p7	15:58993903	AGAAAATTTAAGAAA[A/T]TCTATATATGGCTAG	54778
rs192666722	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59088685	TTGCTGCAAACACTG[A/G]ATTAGCAAATATGGG	54778
rs192677179	snp	C/T	0.0256215	0.110247	upstream-variant-2KB	RNF111	GRCh38.p7	15:58986366	GGGGTTACAGGCGCC[C/T]GCCACTACGCCCGGC	54778
rs192771158	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58998105	AGACGTGGTTTCACT[A/G]TGTTGGTGAGGCTGG	54778
rs192784340	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59087426	CAGTCGAAAATCAGA[A/G]TATAACTTTTGAGTT	54778
rs192786194	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59031845	ATATAAATTACCAAT[C/T]GCAGTATTAAACCAT	54778
rs192801525	snp	A/G	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59064653	TTGTATTTTTCTTCC[A/G]TCCAAGTTCACAGAC	54778
rs192823547	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59035211	CCCTGTCCATGACAC[A/G]TGGGAATTATTATAA	54778
rs192834814	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59068560	GTAGTGAGCCAAGAT[C/T]GTGCCACTGCACTCC	54778
rs192865346	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59068709	ACTTTTCTATGTCAC[C/T]CGACCTTTCCTAAAG	54778
rs192903788	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59001711	ATCATGTGATATAAG[A/G]TTTGTTACAGAACAC	54778
rs192937104	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59008984	TATTTTTTTGAGACA[A/G]AGTCCCATTCTGTCA	54778
rs192950428	snp	A/G	0.00517822	0.0506191	intron-variant	RNF111	GRCh38.p7	15:59042041	TTAGAAGCTTTTTAT[A/G]TATTAGCAATGTAAG	54778
rs192975546	snp	C/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59016128	AGGCATGAGTCACTG[C/T]TCCTGGCCAATTTTG	54778
rs192992869	snp	A/C	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59047707	CAGCCTCCCAAGTAT[A/C]TGGGACTACAGGCAT	54778
rs192996908	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59072100	CATTTTTTAAAAATG[A/C]CAGCAATCCTCTGAG	54778
rs193006735	snp	G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59022661	TCTTTGGGTTTAGGT[G/T]GTTTAACCTCTTCAC	54778
rs193009432	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59046952	GGCTCACTGCAGACT[C/T]GGCCCCCTGGTTTCA	54778
rs193060056	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59084655	TCGCAGTTTTGAAAT[A/G]AACGGTACGTTATTC	54778
rs193088018	snp	G/T	0.00438332	0.0466095	intron-variant	RNF111	GRCh38.p7	15:58990386	AGCTGTGGGCCAGGC[G/T]TGGTGGCTCACCCCT	54778
rs193133458	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59026310	TTTTTTTTTAGCTAT[C/T]GTATTTTCTTAGTGC	54778
rs193140015	snp	A/G	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:59059584	TTCTGGGGTTTTTTG[A/G]TTATGGTTTGGTCTG	54778
rs193160495	snp	A/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58992856	TAAAATAAAATAATA[A/T]ATTTTTGAAAACGTT	54778
rs193208836	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59006064	GTATATTTTTATCTC[C/T]AGTAGGCGTGGTCAT	54778
rs193248409	snp	A/G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59029161	TCAGCAATATATGAG[A/G/T]GTTCCAATGTTTTTT	54778
rs193292524	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59075290	TCTGCAAAGCACTAA[A/G]TGTGCCTATAAAATG	54778
rs193296127	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59042736	TGTTAAATTTTCCAC[A/G]TGCATTTGGGCCTGT	54778
rs199500618	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59054640	TAACTTTATACTCCT[C/T]CTTAAGAATTTTATT	54778
rs199550937	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59026767	AGCGATGGATTTTAG[-/A]AAAAAAAAATAGTAT	54778
rs199581700	snp	A/C/G	1.89324e-05	0.00307666	intron-variant	RNF111	GRCh38.p7	15:59085830	ATGTTCTAAAAGTTC[A/C/G]TTTTCTAAGTATTTT	54778
rs199608380	in-del	-/TGG	0.0667028	0.170006	intron-variant	RNF111	GRCh38.p7	15:59028099	CCAAAGTGTAGGGTT[-/TGG]TGGCCACCGCGCCTG	54778
rs199616519	snp	C/G	0.00199802	0.0315439	missense	RNF111	GRCh38.p7	15:59031075	GGTAACCAGCAAGAA[C/G]AAGAAAAAAGTCTCG	54778
rs199619968	snp	C/T	0.00214698	0.0326938	synonymous-codon	RNF111	GRCh38.p7	15:59091130	GACAATTGAAAGATG[C/T]ACATATCCACATAAA	54778
rs199624176	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59090212	GTGGTTTGTTTTTTT[G/T]TTTGTTTGTTTGTTT	54778
rs199637531	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59035627	CTCTGCTTCCTCTCG[A/C]ATGGTTTGCTCTTAG	54778
rs199687947	snp	C/T	0.000312992	0.0125059	synonymous-codon	RNF111	GRCh38.p7	15:59066972	TACTCCCCACCCAGC[C/T]GTCCCAGTTTCTCCT	54778
rs199689779	in-del	-/C			intron-variant	RNF111	GRCh38.p7	15:59040928	ACCTAGCTTCAGAGT[-/C]AAAACTTTAAAACAA	54778
rs199697814	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59055529	TAGGTCAATTAGTTT[A/G]CCGAGTGCCAGTCAT	54778
rs199765687	in-del	-/TA	0.00953873	0.0683987	intron-variant	RNF111	GRCh38.p7	15:59020135	ATAAAATACATATTT[-/TA]TATATGTTAGATATA	54778
rs199771747	in-del	-/TATTTTATTT	0.00835141	0.0640778	intron-variant	RNF111	GRCh38.p7	15:59008949	GTTAATATTGTCACG[-/TATTTTATTT]TATTTTATTTTATTT	54778
rs199781862	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59074793	GTGCAAGAGGCCTAG[C/T]TTTTGGCCTCTCTGG	54778
rs199835400	snp	A/G	1.64822e-05	0.00287068	synonymous-codon	RNF111	GRCh38.p7	15:59031071	GAATGGTAACCAGCA[A/G]GAACAAGAAAAAAGT	54778
rs199884916	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59049832	GGCTCACTGCAACCT[C/T]TGCCTCCCAGGTTCA	54778
rs199895340	snp	A/C/G	8.24469e-05	0.00642008	synonymous-codon	RNF111	GRCh38.p7	15:59058369	AGAACCTACTGTAGT[A/C/G]CCAACCACTTCTGCA	54778
rs199900517	in-del	-/TTTT	0.488965	0.0734569	intron-variant	RNF111	GRCh38.p7	15:59000164	GATTTTTTTTTTCCC[-/TTTT]TTTTTTTTTTTTTTG	54778
rs199902179	snp	C/T	0.000399281	0.0141238	missense	RNF111	GRCh38.p7	15:59076111	CCCCAAGTCAACCTT[C/T]ATCATCAATAGATGG	54778
rs199951383	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59029585	TAACATGGGAGACCT[A/G]TAAGATTATATATTT	54778
rs199954505	in-del	-/T	0.198944	0.244731	intron-variant	RNF111	GRCh38.p7	15:59050066	TTTCTTTTTTTTTTT[-/T]GTTTTGAGATGAAGT	54778
rs199967891	snp	A/C	0.000648147	0.0179904	missense	RNF111	GRCh38.p7	15:59031666	TTGTTTGTTTCTGCC[A/C]GTGAAAACCACCAAA	54778
rs200024876	snp	C/G	0.00199794	0.0315432	missense	RNF111	GRCh38.p7	15:59058542	GTACCACTGGCACTT[C/G]TATAGGAGGTATGTA	54778
rs200085319	in-del	-/T	0.0115144	0.0749975	intron-variant	RNF111	GRCh38.p7	15:59002106	TGTTTATTTCTAGAG[-/T]TTTTTTCTTTAATAT	54778
rs200091286	in-del	-/GCG	0.0158469	0.0875917	utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58987717	GGCGGCGGCGGCGAA[-/GCG]GCGGCGGCGGCGGCT	54778
rs200107318	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59000190	TTTTTTTGAGACAGG[G/T]TCTCTCTCTGTTACC	54778
rs200128935	snp	A/C/T	3.3099e-05	0.004068	intron-variant	RNF111	GRCh38.p7	15:59094741	ACTACGTACAATTAT[A/C/T]ATAAAATTAATTTTT	54778
rs200132830	snp	A/C	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59056491	AGGAAATGGTCACTC[A/C]TAATTTCCCAAAAGG	54778
rs200160196	snp	A/G	0.00206032	0.0320299	intron-variant	RNF111	GRCh38.p7	15:59081296	CAACGTATGTTTTAC[A/G]TTTTTAAAAAGAAAG	54778
rs200198056	in-del	-/GA			intron-variant	RNF111	GRCh38.p7	15:59004912	AGATGCTCACATTCT[-/GA]GAGACACTTGGGAAG	54778
rs200229978	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59024940	ATTTGTCTTGTTGTG[C/T]CTTCTTATTTCACTT	54778
rs200233097	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59053879	ATCTCTTATTGTTAT[C/T]AAGAGATATTAATTT	54778
rs200233595	in-del	-/GTGTTTTGTTTG			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986203	TGTGTGTGTGTGTGT[-/GTGTTTTGTTTG]TTTGTTTGTTTGTTT	54778
rs200285514	snp	C/T	0.000189912	0.00974268	intron-variant	RNF111	GRCh38.p7	15:59030801	TCTAATTTTGTCTTC[C/T]AGGCTTTCCTTAAAG	54778
rs200316505	snp	A/G	0.000283851	0.0119099	intron-variant	RNF111	GRCh38.p7	15:59076258	TCTAGAGTCATGTCA[A/G]TGAAGCATTTTGTAC	54778
rs200330460	snp	A/G	3.29745e-05	0.00406031	missense	RNF111	GRCh38.p7	15:59031025	AATTCTCTCACCTGT[A/G]TGATGATTCTCAAAA	54778
rs200399712	snp	C/T			synonymous-codon	RNF111	GRCh38.p7	15:59066945	TTTTCAACATCATCA[C/T]CACCACCACCATACT	54778
rs200408888	in-del	-/C			intron-variant	RNF111	GRCh38.p7	15:59094741	ACTACGTACAATTAT[-/C]ATAAAATTAATTTTT	54778
rs200414271	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:58993361	TAAAAACACAAAAAT[-/A]AAAAAAATATAACTG	54778
rs200448671	snp	C/G/T	0.000106222	0.00728703	intron-variant	RNF111	GRCh38.p7	15:59085809	GAAAATTTTCAAAAT[C/G/T]TTGACATGTTCTAAA	54778
rs200574313	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59062051	ATTTGTTTTAAACTT[C/T]TTTTTTTTTTTTTTT	54778
rs200584027	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59017827	CAATGGCACAATCTC[A/G]GCTCTCTGCAACCTC	54778
rs200592840	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59024465	GCAAGATCTTTTCAG[C/T]AAGTACTTTAAGAAA	54778
rs200630040	in-del	-/AG	0.00716266	0.059414	intron-variant	RNF111	GRCh38.p7	15:59036482	ACATGGCAGCAGGCA[-/AG]AGAGAGCTTGTGCAA	54778
rs200694454	snp	C/T	0.00199792	0.0315431	missense	RNF111	GRCh38.p7	15:59052311	TGTTTCCAGGAAGTA[C/T]TGATGAAGATGTTGT	54778
rs200705457	in-del	-/TATT	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59001946	AAAAATTTATAACTA[-/TATT]TAATAAAAATTGTGT	54778
rs200719880	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59070059	TTTTTTTTTTTTTTT[A/T]AGAGAGGATCTTGCC	54778
rs200747794	snp	C/T	4.94637e-05	0.00497287	synonymous-codon	RNF111	GRCh38.p7	15:59075977	GCCAGTGGACCTGAG[C/T]AACAGTGGTATCAGA	54778
rs200793909	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59041962	ATCAGTCTGTTCATA[-/T]TTTTTTTTTTTTTTT	54778
rs200798645	snp	A/T	0.00199792	0.0315431	missense	RNF111	GRCh38.p7	15:59031254	TTCTCCTTCATCTAG[A/T]CTGCATTTTGGAGAT	54778
rs200802668	snp	A/G	0.00199806	0.0315443	synonymous-codon	RNF111	GRCh38.p7	15:59091154	ACATAAATACAAAAA[A/G]GTAAGAATTTATTCT	54778
rs200822277	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:58999046	AACTGCCTTTGTAAA[C/G]TTTTGGGGTAGTATC	54778
rs200823084	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58998476	TTGGGAAGGTTGTTA[C/T]AGGGTCTTCCATTGC	54778
rs200826350	snp	G/T	0.00231114	0.033915	intron-variant	RNF111	GRCh38.p7	15:59089641	ATTCTTAAAATTGAT[G/T]TAGCCTATCTCTTCT	54778
rs200845223	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59094297	CACAATAAGACATTT[G/T]TTAGTGAGGAAAGTG	54778
rs200903466	snp	A/C	0.000399281	0.0141238	synonymous-codon	RNF111	GRCh38.p7	15:59031572	AAAATATGCCTTGCT[A/C]CCTAGTTCTAGTAGT	54778
rs200951132	in-del	-/TTTG	0.00478085	0.0486577	intron-variant	RNF111	GRCh38.p7	15:58989395	TCTCTCTCCTGCTCA[-/TTTG]TTTGTGACCAAAGAT	54778
rs200975904	in-del	-/TTTTTTTT			intron-variant	RNF111	GRCh38.p7	15:59017754	TTATTTGTTGAACTC[-/TTTTTTTT]TTTTTTTTTTTTTGA	54778
rs200981148	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59051791	AATAAATAAATAAAT[A/G]AATAAATAAATAAAT	54778
rs200981342	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58993427	CCTGTAATCCCAGCT[A/G]CTTGGGAGGCTGAGA	54778
rs201011939	in-del	-/AT			intron-variant	RNF111	GRCh38.p7	15:59073491	TCTCCAAAAAAAAAA[-/AT]AAAATAAATAAACTA	54778
rs201014242	in-del	-/TAT	0.00953873	0.0683987	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021629	TTATGAGGTAAGTAC[-/TAT]TATTATTATTCCAAT	54778
rs201034758	snp	A/C/T	0.000683546	0.0184755	synonymous-codon, missense	RNF111	GRCh38.p7	15:59055746	AGTTCTCATGCAAGT[A/C/T]GGCCACAGGAGCCAC	54778
rs201040277	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59060804	TTATTATTATTATTA[-/T]TTATTTTTTTTTTTG	54778
rs201081719	snp	C/T	8.24355e-05	0.00641957	missense	RNF111	GRCh38.p7	15:59031360	AGAAGCCATAGTGCA[C/T]GGTCTCATAAGTGGC	54778
rs201109332	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59000163	TGATTTTTTTTTTCC[C/T]TTTTTTTTTTTTTTT	54778
rs201146966	snp	C/T	0.00199806	0.0315443	intron-variant	RNF111	GRCh38.p7	15:59066748	GATTATTCTGTGCAT[C/T]TTTTTCTGTTTCAAG	54778
rs201171332	snp	C/T	0.000399281	0.0141238	missense	RNF111	GRCh38.p7	15:59081055	ATTCCTCATCCTGTA[C/T]ATGCTTTCCATTCTC	54778
rs201199902	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59055528	TTAGGTCAATTAGTT[G/T]ACCGAGTGCCAGTCA	54778
rs201219303	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59083877	TAATGTTAAAATTAC[C/T]TTTTCCTTGGGTGAT	54778
rs201271056	snp	A/C/G	0.00202837	0.0317846	intron-variant	RNF111	GRCh38.p7	15:59085654	TGTTCTCATCCTTTC[A/C/G]TTAGGGAACTGGGAA	54778
rs201271647	in-del	-/CTTC	0.00914312	0.0669923	intron-variant	RNF111	GRCh38.p7	15:59067166	TTTCTCTCTCTTCCT[-/CTTC]CTTCATTCCTGTCTC	54778
rs201296579	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59025736	TGGCTTTTTTTTTTT[C/T]TTTTTTCTTTTGTGT	54778
rs201328201	snp	C/T	3.29478e-05	0.00405867	synonymous-codon	RNF111	GRCh38.p7	15:59081060	TCATCCTGTACATGC[C/T]TTCCATTCTCAAATA	54778
rs201334024	snp	C/T	1.64741e-05	0.00286998	missense	RNF111	GRCh38.p7	15:59067022	GCCCTGTGGAAAGAC[C/T]TCCACAAGTACAAGC	54778
rs201440226	snp	C/T	0.000429305	0.0146447	missense	RNF111	GRCh38.p7	15:59031444	CATGGCAGTTCGTTA[C/T]GGAGACTTCCATGCA	54778
rs201447006	in-del	-/C			intron-variant	RNF111	GRCh38.p7	15:59081533	CAGCAACAACAACAA[-/C]AAAAAACCATGAAGT	54778
rs201452276	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59027544	TTTCTTTTTTTTTTT[-/T]GGGAGACAGAGTCTT	54778
rs201458419	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59024466	CAAGATCTTTTCAGC[A/T]AGTACTTTAAGAAAG	54778
rs201470570	in-del	-/TTT			intron-variant	RNF111	GRCh38.p7	15:59060818	ATTATTTTTTTTTTT[-/TTT]GTGAGACAGGTCTGA	54778
rs201489807	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59019550	TTTTCATATGGGTTT[-/A]TACACCATTCTTGTC	54778
rs201513331	snp	A/G	6.59055e-05	0.00574007	missense	RNF111	GRCh38.p7	15:59058409	TCACAAGCTACTAGC[A/G]CTTCCATTAACAATT	54778
rs201568227	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59039722	TTTAAGAACTCCTGA[-/T]TTTTTTTTTTTTTGA	54778
rs201570889	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59026294	TTTTGAAAGTTAGTA[-/T]TTTTTTTTTAGCTAT	54778
rs201634546	snp	G/T	0.00299544	0.0385843	intron-variant	RNF111	GRCh38.p7	15:59092458	GTTTTGTTTTGTTTT[G/T]CAAATAAACACAGAC	54778
rs201703137	snp	A/G	0.000399281	0.0141238	synonymous-codon	RNF111	GRCh38.p7	15:59031011	TAAAGTGGGGAATGA[A/G]TTCTCTCACCTGTGT	54778
rs201749960	in-del	-/A	0.0614824	0.164198	intron-variant	RNF111	GRCh38.p7	15:59018551	TTTTTAGAAAAAAAA[-/A]CAAACTATATATACA	54778
rs201771948	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:58999163	TTTCTTATAATTTAA[C/G]CAGAACAGCATATCA	54778
rs201788839	in-del	-/TA/TATTA/TTT			intron-variant	RNF111	GRCh38.p7	15:59060808	TATTATTATTATTAT[-/TA/TATTA/TTT]TTTTTTTTTTGTGAG	54778
rs201789684	snp	A/G/T	1.64757e-05	0.00287012	missense	RNF111	GRCh38.p7	15:59076062	GTTTCTTCCTCCCGA[A/G/T]CTGCAATCTTTGGCC	54778
rs201792467	snp	C/T	0.000247809	0.0111285	intron-variant	RNF111	GRCh38.p7	15:59085639	TAAGGAGGATTAAAC[C/T]GTTCTCATCCTTTCG	54778
rs201824992	snp	A/G	1.78592e-05	0.00298819	intron-variant	RNF111	GRCh38.p7	15:59080914	GTGCCTATGTAACAT[A/G]CTCAAAATATTTTTC	54778
rs201911328	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59000178	CTTTTTTTTTTTTTT[G/T]TTTGAGACAGGGTCT	54778
rs201920011	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59083143	CAAGATTCTGCCGCT[A/T]AAAAAAAAAAAGAAG	54778
rs201949013	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59043158	TGTACAATTTAGTAA[-/T]TTTTTTTTTTTTTTG	54778
rs201949306	snp	C/T	0.0410537	0.137264	intron-variant	RNF111	GRCh38.p7	15:59067235	CTCCCTGCCTCCCTC[C/T]GTTTCCTTTTTTTTT	54778
rs201976489	in-del	-/TTTGTTTG			intron-variant	RNF111	GRCh38.p7	15:59090209	GTTGTGGTTTGTTTT[-/TTTGTTTG]TTTGTTTGTTTGTTT	54778
rs202013227	snp	A/G			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986702	GTATTTTTAGTGGAG[A/G]AGGAGTTTCACCATG	54778
rs202021176	in-del	-/C			intron-variant	RNF111	GRCh38.p7	15:59093359	TTTTTTTTTTTTTTT[-/C]TTCCTTTTCTGGGAG	54778
rs202096125	snp	A/T	0.003211	0.0399399	missense	RNF111	GRCh38.p7	15:59030928	GAGAGTCTGAAAGGG[A/T]TCCTTTTGCATCCAG	54778
rs202115445	in-del	-/ACTCC			intron-variant	RNF111	GRCh38.p7	15:59067256	CTTTTTTTTTTTTTA[-/ACTCC]CTCCCATTCTTCCTT	54778
rs202130384	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59023536	GTGTTATTTTTATTT[A/T]TATATTTTTGGTAAA	54778
rs202215514	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59067254	TCCTTTTTTTTTTTT[A/T]AACTCCCTCCCATTC	54778
rs202216064	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59019210	TCACAAAGTGCTGGG[A/T]TTACAGGTGTGATCC	54778
rs202216234	snp	A/G	3.29712e-05	0.00406011	missense	RNF111	GRCh38.p7	15:59058373	CCTACTGTAGTACCA[A/G]CCACTTCTGCAAGAA	54778
rs367552075	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59093451	CCTGGGCTGAAGCGA[C/T]CCACCTACCTCAGCC	54778
rs367596801	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59067411	ACCCAGCATGAGGGA[G/T]TAACTACTTGCGTTA	54778
rs367600114	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59051221	CACTTTGGGAGGCTG[A/T]GGAGGGTGGATCATG	54778
rs367601596	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59007384	TTTTTGAGATTAATC[C/T]GTATTGATACATGTA	54778
rs367640621	snp	C/T	0.430136	0.173352	intron-variant	RNF111	GRCh38.p7	15:59049745	TCTTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT	54778
rs367799070	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58989507	CTCCTTGTTTATCAC[A/G]GGTGCTATATCATGT	54778
rs367819366	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59009263	TGCGCCTGGCCACGT[A/G]TTTTACTTTTACATG	54778
rs367850460	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:58995972	TCAGGACATCGCTAG[C/G]AAACTAAATTTAAAT	54778
rs367876952	snp	G/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59020031	AATGGGGTTAATGGA[G/T]TTTTGAGTTTAGTTC	54778
rs367940632	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:58992162	CAATTCTTCTGCGTC[A/T]GTCTCCTGAGTAGCT	54778
rs368008199	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58992137	GAAGCCTCCACCTCC[C/T]GGGTTCAAGCAATTC	54778
rs368012004	snp	C/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:58996312	GTGCGGTAGCTCATA[C/T]CTATAATCCCAGCAC	54778
rs368039482	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59067603	ATGGACTAAATTATT[A/G]CAACTAATTGAATGG	54778
rs368044663	snp	A/G			missense	RNF111	GRCh38.p7	15:59031357	AGTAGAAGCCATAGT[A/G]CACGGTCTCATAAGT	54778
rs368049097	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59049746	TTTTTCTTTCTTTCT[-/T]TTTTTTTTTTTTTTT	54778
rs368063004	snp	C/T	3.29457e-05	0.00405854	synonymous-codon	RNF111	GRCh38.p7	15:59058477	TTCAGCTGTCACCAG[C/T]AGCCAACCTTCCACA	54778
rs368113937	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59060976	TGTATTTTAGTAGAG[A/T]TGGGGTTTTGCCATG	54778
rs368126554	snp	A/G	1.64996e-05	0.0028722	missense	RNF111	GRCh38.p7	15:59031582	TTGCTACCTAGTTCT[A/G]GTAGTTCCAGTGAGA	54778
rs368126860	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59075882	TTGGTTATATTAGGA[A/G]TACTTTTATAATATA	54778
rs368179840	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59079977	AAAAAGGTGAGTAAT[A/G]CAATAGGCTAAGCAT	54778
rs368217654	snp	C/T	0.00993419	0.0697739	intron-variant, utr-variant-5-prime	RNF111	GRCh38.p7	15:58988186	GAAGGCTGGGGTCGG[C/T]GACCGGCCGGTTATC	54778
rs368228550	snp	A/C/T	5.4965e-05	0.00524214	intron-variant	RNF111	GRCh38.p7	15:59055876	AACAGTAGAAAATTA[A/C/T]GAAAGGAGTTTGATA	54778
rs368287693	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59026900	AACACACACCACAGC[A/G]TACACCAAACCACCC	54778
rs368382104	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59024461	GCTAGCAAGATCTTT[G/T]CAGCAAGTACTTTAA	54778
rs368421943	snp	A/T	0.000116062	0.00761693	missense	RNF111	GRCh38.p7	15:59031647	AACTGAAGGAGAAGA[A/T]GATTTGTTTGTTTCT	54778
rs368437583	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59064535	AGCAAGACTTTGTCG[A/C]AAAAAAAAAAAAAAA	54778
rs368472755	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59072687	TCAATCTCCTGACCT[C/T]GTGATCTGCCTGCCT	54778
rs368538432	snp	A/G	0.00914312	0.0669923	intron-variant	RNF111	GRCh38.p7	15:59025834	CTTGCGGATTCAAGC[A/G]ATTCTCCTGCCTCAG	54778
rs368544169	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59012372	ATTTGATAATTAAGA[C/T]CCTTAGCCTTTAGTG	54778
rs368571487	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59092963	TTTGAGCACACCACA[A/C]TGCACTCCAGCCTGG	54778
rs368576198	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59015373	ATAGTTTTACAATAG[C/T]ATTGAAATATTTTAT	54778
rs368595732	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59056898	TAGGAGAAGGTGATA[A/G]AGTAGCCTTTTCCAC	54778
rs368598719	snp	A/G	4.94425e-05	0.0049718	missense	RNF111	GRCh38.p7	15:59031106	TTGTGAGGAAAAAAC[A/G]CAAAAGCCAGCAGGC	54778
rs368624610	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58996838	ATTAATATCTGTACA[C/T]GGTTTTAAAAGTCAG	54778
rs368635583	snp	A/G	1.66167e-05	0.00288237	intron-variant	RNF111	GRCh38.p7	15:59058587	GGGAGACTTTTTGTC[A/G]TTACTTTCGTTAGGA	54778
rs368640767	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59040145	TTAAAGGGACGGTCT[C/T]ACTCTGTTGCCTAGG	54778
rs368702448	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59018962	AGCGCCATGCTCTGT[C/T]GCCCAGGTTGGAGTG	54778
rs368709420	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59064730	GGAGATTAGCCCCCA[C/T]AGGCCAGACTAGCAG	54778
rs368714634	in-del	-/A	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59026988	AGCAGATTTAACCAT[-/A]AAGAGTTGATTGCAT	54778
rs368743394	snp	A/G	3.80909e-05	0.00436394	intron-variant	RNF111	GRCh38.p7	15:59084091	ATAACCAATTATTCA[A/G]TTATTTCCAGTGGTC	54778
rs368763629	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59053189	TGCTCTGAACTAACA[C/T]ATTAATGAAACATCC	54778
rs368776701	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59088657	CTATGCATGGCAGTT[A/G]TGATCTATACAGTTG	54778
rs368793815	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59078863	GTCTCCCTCTCAAAA[A/G]AAGAAAAAAAAAAAA	54778
rs368794426	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59028703	TTTATAAGTTTTTTT[-/T]ATGAATATGTGTTTT	54778
rs368794889	snp	A/G	1.66095e-05	0.00288175	intron-variant	RNF111	GRCh38.p7	15:59076234	AGTATATACTTAGTG[A/G]ACACAAAATCTAGAG	54778
rs368798722	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59084027	ATGACTAATCTATAG[A/G]TGTTTATAGTATTAA	54778
rs368803129	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59068676	AGGCATTAAGCCACC[A/G]TGCCCGGCCAAGCTA	54778
rs368810055	snp	A/T			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:58988077	GATTAAGGTGAGGGG[A/T]ACGGGGGGGGAGGGG	54778
rs368811268	in-del	-/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59048489	AGGACTTGCGAGCTC[-/T]TTTTGGGGTTATTGG	54778
rs368817504	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59023462	AGTATATTTTTGTTA[C/T]TCTGTAGTATTTTCT	54778
rs368817595	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59084427	AGAGGAAAGAATAGG[A/G]GCTGGGGCAGGGAAC	54778
rs368840094	snp	C/T			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021732	CAGTGATCCCTGGAT[C/T]GAAAATCTACATCAC	54778
rs368855736	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59010504	CCTCCTAGGTTTAAG[C/T]GATTCTCCTGCCTCA	54778
rs368856371	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59061776	CCTTAGTACATGCAC[A/G]TGTACACTTGTTTTT	54778
rs368858550	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59068524	GGCAGGATAATCACT[C/T]TAACTTTAGAGGTGG	54778
rs368859629	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59063142	TTGGCGCTTAGCTAC[A/G/T]TGATTGCATGCTGCT	54778
rs368861956	snp	C/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59037422	TTAATTTTAGTAATA[C/T]ATTTCTAGGATCTAT	54778
rs368870962	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59003203	TCACTGCAACCTCTG[C/T]CTCCTGGGCTCAAGC	54778
rs368888025	snp	A/G			utr-variant-3-prime	RNF111	GRCh38.p7	15:59095320	AATTTAATCAATCAT[A/G]TACTTTAGTTTAATG	54778
rs369075153	snp	C/G	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59022995	CTTACGCCTGTAATC[C/G]CAGCACTTTGGGAGG	54778
rs369078940	snp	C/G	1.64741e-05	0.00286998	missense	RNF111	GRCh38.p7	15:59081163	CCTCAGCATCTTCCT[C/G]CTACACACCAGCCAA	54778
rs369117729	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59019196	CACCTGCCTTGGCCT[C/T]ACAAAGTGCTGGGAT	54778
rs369166271	snp	C/T	0.000115332	0.00759293	missense	RNF111	GRCh38.p7	15:59066829	GCAATGCCAAGGTTA[C/T]CTTCCTGCTGTCCCC	54778
rs369226007	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59037562	ATAGGTATTGCCGGG[A/C]GTGGTGGCTCACACC	54778
rs369237807	in-del	-/GG			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:58988086	GAGGGGAACGGGGGG[-/GG]AGGGGATCCATTGGA	54778
rs369287485	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58994202	GCTACCACGCTCAGG[C/T]TATTTTTTATATTTT	54778
rs369292354	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59046298	TCCAGGGCTAAGGTG[A/G]TCCTCCCACGTCAGC	54778
rs369303991	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59085363	TGCTCCTCAAGTAGA[A/G]TCAGACTTTTATCTT	54778
rs369357869	snp	C/T	3.29544e-05	0.00405908	missense	RNF111	GRCh38.p7	15:59076045	TTGACCCCTGCTGCC[C/T]TGTTTCTTCCTCCCG	54778
rs369395960	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59000836	TTATTTTAAAGAACA[A/G]TTCAGCAAATGCCTA	54778
rs369398252	snp	A/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59027576	CTCTGTTGCCCAGGC[A/T]GGAGTGCAATGGCGC	54778
rs369420427	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59045401	TTACCATGTTGGCCA[C/G]GCTGGTCTCGATCTC	54778
rs369430376	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59084957	TCTGACCCCCACCTT[C/T]GTACTCAGATTTGCT	54778
rs369434704	snp	C/G	1.67419e-05	0.00289321	missense, intron-variant	RNF111	GRCh38.p7	15:59084119	GTCTTTTTGTGTTCT[C/G]TGTTTCCAGGCGGGC	54778
rs369434767	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59054043	TGGGTTCAAGCAATC[C/T]TCCTCCCTCAGCCTT	54778
rs369459170	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59072826	ACTTTTGCTGCAGTT[G/T]TTTGTTTGTTTGTTT	54778
rs369471833	snp	A/C	3.29489e-05	0.00405874	missense	RNF111	GRCh38.p7	15:59066989	TCCCAGTTTCTCCTT[A/C]CTTTAGTGATCCTGC	54778
rs369494531	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58992745	GGATGGCTTGAGCCC[A/G]GGAGGCAGAGGTTGC	54778
rs369634188	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59034175	TCTCATTCTTCTTGA[A/C]ATTTGCATAGTATTC	54778
rs369643178	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59076490	TTTTAAGAATTCTCA[A/G]GCAGTTAGCTGAGAC	54778
rs369710167	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59073932	GTGTTAGGTATGAAA[A/G]CATTAATCTACTTAT	54778
rs369845274	snp	A/G	0.000574126	0.0169332	intron-variant	RNF111	GRCh38.p7	15:59092498	TTGTTCAATAATGTC[A/G]TCTCTACTAATAAGG	54778
rs369858565	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59042610	GGTGTTTATCCTTAC[A/G]TATAATAGGAAAAAT	54778
rs369864794	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:58993278	CTTTGGGAGGCCAAG[G/T]CGAGTGGATCACCTG	54778
rs369916832	snp	C/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59079130	GCAACCTGTTTTGTT[C/T]AAACAGTGAATTAAA	54778
rs370030661	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59080729	GTGAGTGAAGTTAAA[C/G]TATAATATATATATT	54778
rs370032867	snp	C/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59058861	CAAAATTTAGAACTT[C/T]CGTGCATTAAAGGAT	54778
rs370036661	snp	A/G	0.000329495	0.0128312	synonymous-codon	RNF111	GRCh38.p7	15:59081021	TCAGACTCAGCCTCC[A/G]CCTCAAGTGGATTAT	54778
rs370115814	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59019572	ATTCTTGTCAGGCTT[A/T]ATACCTTGGAATAAC	54778
rs370136355	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59030154	TGTTTATTTAACTGA[A/G]TGATCTTCAGCAGCC	54778
rs370141360	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59026243	CACATAAACTTGTTT[A/G]TGATGTGAATTACTA	54778
rs370164163	snp	C/T	1.64762e-05	0.00287016	synonymous-codon	RNF111	GRCh38.p7	15:59058414	AGCTACTAGCGCTTC[C/T]ATTAACAATTCAAAT	54778
rs370186995	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59039117	TTACAGGCACGTGCC[A/G]CCATACCTGGCTAAT	54778
rs370233940	snp	A/T	1.64885e-05	0.00287123	missense	RNF111	GRCh38.p7	15:59067051	GCACCTTGTGGAGCA[A/T]ATAGTAGTTCTGGTA	54778
rs370256013	snp	A/G			missense	RNF111	GRCh38.p7	15:59055740	GGTTCCAGTTCTCAT[A/G]CAAGTCGGCCACAGG	54778
rs370261363	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59030001	GTCATGATATTTACT[A/G]TTACATTATTTTCAT	54778
rs370266684	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59078961	TGGGAATGCAGTGAG[C/T]AAATGTTGGAATAAA	54778
rs370378410	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59067435	TGCGTTAAAACCAAC[C/T]CACCTTTCTTTTTTA	54778
rs370396542	in-del	-/ATT			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021639	AGTACTATTATTATT[-/ATT]CCAATTTTATAGACT	54778
rs370412120	snp	C/G	1.6596e-05	0.00288058	intron-variant	RNF111	GRCh38.p7	15:59075950	ATACTTCCTTTTTAT[C/G]TAGCAGGCATTGCCA	54778
rs370460647	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58996112	ATACATAATGAGTTA[C/T]GTTCTTAATTGTGAT	54778
rs370492090	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59011993	TTAGTGTTCTTTTTT[G/T]TTTGTTTGCCTTTTT	54778
rs370533213	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59062337	TGTGAGCCACCATGC[A/C]CGGCCATTTTAGACT	54778
rs370533517	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096040	AATTATACTGTCAAC[C/G]TACTGTTGCTATGGT	54778
rs370580414	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59001608	CTCTCCACATTTGGC[C/G]AATAGGTTCACTTTA	54778
rs370647407	snp	C/T	0.000132258	0.00813089	intron-variant	RNF111	GRCh38.p7	15:59094748	ACAATTATCATAAAA[C/T]TAATTTTTGCTTTTT	54778
rs370671191	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59066595	GCCTGTGCAACAACA[A/G]CAAGACTCCATCTCA	54778
rs370702925	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59067546	AATGGCCTAATTTAG[G/T]GGTCTGTAGTTTCTT	54778
rs370720786	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59059661	ATTTATTCTGGAGCT[G/T]TCTTTAGTTTTAGCT	54778
rs370749970	snp	C/T	0.000153988	0.00877327	synonymous-codon	RNF111	GRCh38.p7	15:59031284	TTCTGATACTGTGAC[C/T]TCAGATGAGGATAAA	54778
rs370765449	snp	A/G	9.88338e-05	0.00702902	synonymous-codon	RNF111	GRCh38.p7	15:59058483	TGTCACCAGTAGCCA[A/G]CCTTCCACAGTGTCA	54778
rs370775869	snp	C/T	0.000275968	0.0117434	intron-variant	RNF111	GRCh38.p7	15:59081325	AGTCAAGTTTGCTTT[C/T]TCTTCTACTTCCATT	54778
rs370798894	snp	C/G	3.29592e-05	0.00405938	synonymous-codon	RNF111	GRCh38.p7	15:59031095	AAAAAGTCTCGTTGT[C/G]AGGAAAAAACGCAAA	54778
rs370810672	snp	C/T	0.000150146	0.00866318	intron-variant	RNF111	GRCh38.p7	15:59058323	TTATCTAATTTGTTT[C/T]GAAATGCTAAGTTGA	54778
rs370834886	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58994454	AATGTTGTCACTCTT[A/G]CTTTCTTATTTTCTC	54778
rs370856847	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59012055	AGTCTCGCTCTGTCA[C/T]CCAGGCGGGAATGCA	54778
rs370864376	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59035360	TCTTAACTCATTTCA[G/T]TATTTACTCAAAAGT	54778
rs370924914	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59011441	ACTCAGAAAGTGTTT[A/G]TTCCACAGTGTATTA	54778
rs370937564	snp	A/G	1.66441e-05	0.00288474	synonymous-codon	RNF111	GRCh38.p7	15:59084243	TCGACAGGCTCCAGA[A/G]AGGTCTGCCTGGTCA	54778
rs370956183	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59023934	CTTTCTGGAAGGTGC[A/T]ACCACTTTCCTATTT	54778
rs370962227	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59013946	GGCACACGCCACCAC[A/G]CCTGGCTAATTTTTG	54778
rs371013274	snp	A/G	1.65015e-05	0.00287237	missense	RNF111	GRCh38.p7	15:59076198	TCTCATCATGTCGAC[A/G]TTACATGCCACCCCC	54778
rs371055660	snp	C/G	0.000120593	0.00776414	intron-variant	RNF111	GRCh38.p7	15:59075913	ACATGAAATATTTGA[C/G]CAAACTTTAGAAAGA	54778
rs371065856	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58997620	TCAAGAGATCGAGAC[C/T]ATCCTGGGCAACATG	54778
rs371077410	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59019226	TTACAGGTGTGATCC[A/G]TTTATTTATTTTATT	54778
rs371104464	in-del	-/GCC			intron-variant	RNF111	GRCh38.p7	15:59012001	CTTTTTTGTTTGTTT[-/GCC]TTTTTTTTTTTTTTT	54778
rs371218655	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59000310	CTGGGACTACAGGCA[G/T]GTACCACCACACTTG	54778
rs371302204	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59073488	CCATCTCCAAAAAAA[-/T]AAAAAAATAAATAAA	54778
rs371340946	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59041566	ACTCTGTCTCAAAAG[-/A]AAAAAAAAATTACTG	54778
rs371353832	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59084482	TTTTAGGTGTTATTT[G/T]ATGTTTAATTGAAAA	54778
rs371369584	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59037524	TATGAGGACTTCTTT[A/G]TACTTTATTAACTTT	54778
rs371387974	snp	A/C	1.6686e-05	0.00288838	intron-variant	RNF111	GRCh38.p7	15:59058599	GTCATTACTTTCGTT[A/C]GGAAAAGTATTATTG	54778
rs371401523	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59071978	AGTGACATTATGTTT[A/G]AAAAAATGTACATGC	54778
rs371432146	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59030105	GATTTAGATAGATTA[A/G]CTGTACAAAGTTTGA	54778
rs371434799	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58995608	GATTATAGGCGCCTG[C/T]CACCATGCCCGGCTA	54778
rs371453519	in-del	-/TT			intron-variant	RNF111	GRCh38.p7	15:58994034	TGTTGTTACTTAAAT[-/TT]TTTTTTTTTTTTTTT	54778
rs371484508	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58991404	CTCATGTTCTAGGCA[C/T]AGTCACTGGTCTTCA	54778
rs371553034	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59010993	CCCCTTTTCTCCCTA[A/T]CGGTCATCGTTCTAG	54778
rs371609992	snp	C/T	1.64773e-05	0.00287026	missense	RNF111	GRCh38.p7	15:59031126	AGCCAGCAGGCTGGC[C/T]CTTCGTATGTGCAGA	54778
rs371611853	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59074226	GAATTGCAAATGAGC[A/G]TTGGATTTTAAGTCA	54778
rs371626097	snp	G/T	4.97822e-05	0.00498885	intron-variant	RNF111	GRCh38.p7	15:59085608	CTCCCCATGTCTGTT[G/T]ATAAAAAAGAGACCC	54778
rs371664031	snp	A/G	0.000556298	0.0166685	intron-variant	RNF111	GRCh38.p7	15:59080901	TCATGGAAACCCCC[A/G]	54778
rs371665251	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59060306	TATATATTTTAATTC[C/T]TAAAAAAAAAAAAAT	54778
rs371687041	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59062051	TTTGTTTTAAACTTC[-/T]TTTTTTTTTTTTTTT	54778
rs371723667	snp	A/C			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020673	ATTAAGTTCACTGAG[A/C]AATTGAAACCTATTA	54778
rs371731101	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022317	TTCATTCAGAGCAAG[C/T]CTTAGCTGAGATACT	54778
rs371732082	snp	C/T	0.00716266	0.059414	intron-variant	RNF111	GRCh38.p7	15:59010440	GGAGTCTCACTCTGT[C/T]GCCCAGGCTGGAGTG	54778
rs371749071	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59062040	TTGACCACTATATTT[G/T]TTTTAAACTTCTTTT	54778
rs371793322	snp	A/G	1.65053e-05	0.0028727	missense	RNF111	GRCh38.p7	15:59085748	ATCACGCACCTCCTC[A/G]ACTTCATCACTTACA	54778
rs371793425	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59088849	CGTGAATGAAACTTA[C/T]TCTCTCCATAAGGTG	54778
rs371794178	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:58992276	TCTTGAACTCGTGAT[C/G]TCAGGTGATTCGCCC	54778
rs371796714	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58996315	CGGTAGCTCATACCT[A/G]TAATCCCAGCACTTC	54778
rs371802734	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59014902	CTGGGACATGTGTGC[A/G]CCACCACTCTCCCCT	54778
rs371807688	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59026502	TCACCAAGGAGATAT[A/G]TCTTGTACGCATTTG	54778
rs371817594	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59068730	TTTCCTAAAGTACTT[A/G]CCTCATCTTTTAAAA	54778
rs371938937	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59037732	TCCCAGCTACTTGGG[A/G]GGCTGAGGCAGGAGA	54778
rs371943932	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59057852	ATTCTGATGCTTTCC[C/T]AGTTCTACAGATGAG	54778
rs371958532	snp	C/T	8.34105e-05	0.00645742	intron-variant	RNF111	GRCh38.p7	15:59058597	TTGTCATTACTTTCG[C/T]TAGGAAAAGTATTAT	54778
rs371975270	snp	C/G	0.000153988	0.00877327	missense	RNF111	GRCh38.p7	15:59031622	GCAGTGAATCCTCTT[C/G]TAGCTCATCAACTGA	54778
rs371986810	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59056993	TGCTCCCTTTCCCCC[A/C]ACTAGTTTTTCTCAT	54778
rs371993145	snp	A/G	0.00835141	0.0640778	intron-variant	RNF111	GRCh38.p7	15:59072507	TGCCCAGGCTGGAGT[A/G]CAGTGGCGTGATCTC	54778
rs371998265	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59046704	CCAAAATCACAATCC[A/G]TAAAAGAAGTTGCCA	54778
rs372058587	snp	C/T	0.00716266	0.059414	intron-variant	RNF111	GRCh38.p7	15:59013138	CTCATTTCTCTCCTG[C/T]CTTTCCTAGGGATCA	54778
rs372079123	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58988445	GGGCGCTAAGTCAGC[C/T]CTGACGGCTAGGGAG	54778
rs372081087	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59078866	TCCCTCTCAAAAGAA[A/G]AAAAAAAAAAAAAAA	54778
rs372090758	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59076609	TCACTCCTGTAATCC[C/G]AGCACTTTGGGAGGC	54778
rs372119314	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59068101	ATGATATAAGTCTGC[A/G]TGTTGCAACTCAGGA	54778
rs372131697	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59000518	GGAATTTGAGACCAG[C/G]CTGGCCAACTTGGGG	54778
rs372137954	snp	A/G			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020999	GTGGTGATTTCTGAG[A/G]TTTTGGTGCACCCAT	54778
rs372159066	snp	A/T	1.64727e-05	0.00286986	synonymous-codon	RNF111	GRCh38.p7	15:59066897	TGCATTAGGACATCC[A/T]CATACAAGTTGCTTT	54778
rs372159713	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59019605	TATAGCTATTTTTGT[G/T]GCTTTGGGGAAAGTG	54778
rs372174163	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59064197	GTGAATGAAAGTAAC[A/G]TAATTATAGAACTGA	54778
rs372178063	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59046412	TACCCAGGCTGGTCT[C/T]GCACTCCTGGGCTCA	54778
rs372309780	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58997415	CACTGATGGTGCAAA[A/G]AACAGTGGTGCATTA	54778
rs372327726	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59053384	CACCCAACTAATAAT[C/G]TAACGGATGAATCTT	54778
rs372331835	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59015431	TGTTAGTCACAATTG[G/T]CATGTTAATGTGGTG	54778
rs372340800	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59072364	TCAATCCTTTCAAAC[G/T]TTGCAGCTGCTTTAA	54778
rs372370012	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59061035	CTCCTGGGCTCGAGC[A/G]ATCCACCTGCCTCAG	54778
rs372377778	in-del	-/C	0.495135	0.0490805	intron-variant	RNF111	GRCh38.p7	15:59053878	ATCTCTTATTGTTAT[-/C]TAAGAGATATTAATT	54778
rs372379137	snp	A/C			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021904	TTTGCTCTGTCACCC[A/C]GGCTGAAGTACAGTG	54778
rs372399395	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59064733	GATTAGCCCCCATAG[A/G]CCAGACTAGCAGCTT	54778
rs372405083	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59052963	TTGAAATTTAGATGT[C/G]AATAATACATAAATA	54778
rs372409470	snp	C/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022456	TAACTTTGACTTCCA[C/G]ATTCTGACAGTTCTA	54778
rs372410090	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59059924	TTTAATAATATCTCA[C/T]TTAATTCTTTTAATA	54778
rs372454635	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59026903	ACACACCACAGCATA[C/T]ACCAAACCACCCCCC	54778
rs372457454	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59065927	GAGGCAGGAGAATCT[A/G]TTGAGCAAATATATA	54778
rs372471105	snp	G/T	1.64991e-05	0.00287215	missense	RNF111	GRCh38.p7	15:59067055	CTTGTGGAGCAAATA[G/T]TAGTTCTGGTACCAG	54778
rs372524768	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58990478	AAATGGTGAAACCCC[A/G]TCTCTACTGAAAATA	54778
rs372553411	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59038812	TTGATGATACTGTGT[A/G]CTTTCTGTTGCGTCA	54778
rs372556768	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59023671	TATATATGCCCATTC[C/T]CTTGTTTAAATGAGT	54778
rs372562643	snp	C/T	0.00953873	0.0683987	intron-variant	RNF111	GRCh38.p7	15:59073139	GTTTGTATTACTGCA[C/T]TCCACTGTAGGCAAC	54778
rs372594752	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59005492	CCCGCATTCTCAGGA[C/T]AGCTGTCATCTTTTT	54778
rs372605365	in-del	-/AA			intron-variant	RNF111	GRCh38.p7	15:59018649	CACTCCCAAACTGTT[-/AA]GTGTGTATTTTACAA	54778
rs372625555	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59016642	TTTCAAACAGTATTT[A/C]CTGCCTCTCACAAGG	54778
rs372644905	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59062259	TGTTGCCCAGGCTGG[C/T]CTCGAACTCCTGGAC	54778
rs372851882	snp	C/G	0.000197804	0.00994299	synonymous-codon	RNF111	GRCh38.p7	15:59030960	GCCCATTGGGGCAGC[C/G]AAAAGTTTTCCTGCA	54778
rs372877303	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59041033	CCCCCTTCTCTTACT[C/T]AAAAGTGTCTCTTGC	54778
rs372885262	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59058304	TACATTAAAATATAA[C/G]CCTTTATCTAATTTG	54778
rs372928339	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59070219	TCTGTGTAAGCCAAT[G/T]ATTATGTCCCATCAC	54778
rs372935495	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59045632	TATGGGTTGAAATAA[A/G]GAAAGTTTTTTAAAA	54778
rs372957769	snp	G/T	0.000156986	0.00885823	intron-variant	RNF111	GRCh38.p7	15:59092656	GTAACTAGATATTAA[G/T]TATCTAAAATCCATT	54778
rs373003108	snp	A/C/T	3.29474e-05	0.00405867	missense, synonymous-codon	RNF111	GRCh38.p7	15:59081063	TCCTGTACATGCTTT[A/C/T]CATTCTCAAATATCT	54778
rs373007103	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59059013	CCGGGTGTGATGGCT[C/T]ATGCTTGTAATTCCA	54778
rs373014448	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59020080	ATATCATATAATTTT[A/T]TATTTTGTGTTATAT	54778
rs373091127	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59077979	TTAGTTCACGTGTGA[A/G]ACATGTGGTTCTTAA	54778
rs373152471	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59077449	TCAGAGGTAGTAACT[A/G]TTCTATAAAAACTTT	54778
rs373162379	snp	A/C/G	6.66867e-05	0.00577398	missense	RNF111	GRCh38.p7	15:59055732	GGAGCCAGGGTTCCA[A/C/G]TTCTCATGCAAGTCG	54778
rs373196097	snp	C/T			utr-variant-3-prime	RNF111	GRCh38.p7	15:59095648	AGAATTTTATTTCCC[C/T]GATTCAGTTTTTGCT	54778
rs373234161	snp	A/G	0.000115334	0.00759299	synonymous-codon	RNF111	GRCh38.p7	15:59067035	ACCTCCACAAGTACA[A/G]GCACCTTGTGGAGCA	54778
rs373243485	snp	A/G	4.9436e-05	0.00497148	missense	RNF111	GRCh38.p7	15:59089736	GGAACATCATTCAGA[A/G]GTCCTTTCAGGGGCA	54778
rs373262115	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59049891	GGATTACAGGTGCGT[A/G]CCACCACACCCGGCT	54778
rs373263458	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59082008	TATCCTTGAACTCCT[C/G]TGCTTAAGTGATCCT	54778
rs373265980	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59013716	CCTGAACGAGGGAGT[G/T]TCCACATAAATGTTT	54778
rs373356359	snp	C/G	1.69663e-05	0.00291253	intron-variant	RNF111	GRCh38.p7	15:59084275	TATCTTCTTTAATTT[C/G]AAAACAGTGCTTCAC	54778
rs373418637	snp	C/T	1.64944e-05	0.00287175	missense	RNF111	GRCh38.p7	15:59076188	CAGCCCTCTCTCTCA[C/T]CATGTCGACATTACA	54778
rs373428876	in-del	-/TCTCA			intron-variant	RNF111	GRCh38.p7	15:59059681	TAGTTTTAGCTCTTA[-/TCTCA]AGCTAGTTCTTACGT	54778
rs373459495	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59000948	TGTAGATGGTCATTG[C/T]GGAAATAAGTGAGCT	54778
rs373501971	snp	C/T	1.6504e-05	0.00287258	synonymous-codon	RNF111	GRCh38.p7	15:59084195	TGGTCATGGGCATCA[C/T]ATTCATGTGCCTCAG	54778
rs373511136	snp	C/G	1.92228e-05	0.00310017	intron-variant	RNF111	GRCh38.p7	15:59055888	TTATGAAAGGAGTTT[C/G]ATAAAAGGAAATCTC	54778
rs373569722	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59024772	ACATCTCCATCTATT[A/T]CCACAACTTTTTATC	54778
rs373578855	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59084976	CTCAGATTTGCTCCA[C/T]CACCCTCACCTGCCA	54778
rs373674143	snp	A/G	0.000230639	0.0107362	synonymous-codon	RNF111	GRCh38.p7	15:59031248	TCTTTCTTCTCCTTC[A/G]TCTAGTCTGCATTTT	54778
rs373713832	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59017313	GCATATGTGACAATG[C/G]TTATTCATAAGAGAA	54778
rs373794482	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59055940	CTGCTTACTGGTAAT[A/G]TATTATTAAACTACA	54778
rs373815694	snp	A/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59086096	AGTGGTAATAGATCC[A/G]TTCTGATGCAGTCAT	54778
rs373815787	snp	C/T	4.95274e-05	0.00497607	intron-variant	RNF111	GRCh38.p7	15:59085653	CTGTTCTCATCCTTT[C/T]GTTAGGGAACTGGGA	54778
rs373828810	snp	C/G/T			intron-variant	RNF111	GRCh38.p7	15:59076556	TATATTCATTTGATG[C/G/T]AGGCAATTAAAATAT	54778
rs373843488	snp	A/G			missense	RNF111	GRCh38.p7	15:59031157	ATTGTGTTAAAGAAA[A/G]CCAGGGAATATTAGG	54778
rs373894477	in-del	-/TTTTTTTTT			intron-variant	RNF111	GRCh38.p7	15:58996650	CTCATCAGTACTTTC[-/TTTTTTTTT]TTTTTTTTTTTTTTT	54778
rs373913813	snp	A/G	1.65059e-05	0.00287275	missense	RNF111	GRCh38.p7	15:59031516	AAACAAAAAGAGAGG[A/G]TATTAATGCAGAGGA	54778
rs373927571	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59039206	TAACCTCAGGTCATC[C/T]GCCCGCCTTGGCCTC	54778
rs373939203	snp	C/T			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020781	TACCAAACTCCAGTC[C/T]TCCATAATAGAGGAA	54778
rs373978330	snp	C/T	0.000153988	0.00877327	synonymous-codon	RNF111	GRCh38.p7	15:59076110	GCCCCAAGTCAACCT[C/T]TATCATCAATAGATG	54778
rs374058593	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59024009	AATAATATATAGGAA[A/G]AAATCTTTTGGCTCC	54778
rs374080452	in-del	-/C			intron-variant	RNF111	GRCh38.p7	15:59062051	ATTTGTTTTAAACTT[-/C]TTTTTTTTTTTTTTT	54778
rs374159491	snp	G/T			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986205	TGTGTGTGTGTGTGT[G/T]TTTTGTTTGTTTGTT	54778
rs374162207	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59058775	CTCAAATAAGAGAGC[C/T]TGGGGAGAAGCAAAT	54778
rs374172150	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59072727	AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCA	54778
rs374172420	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59038484	TAAAAGTAGCATTGA[C/T]TGAGTTATAGTTTTT	54778
rs374173350	snp	C/T	3.30644e-05	0.00406585	intron-variant	RNF111	GRCh38.p7	15:59058554	CTTCTATAGGAGGTA[C/T]GTAAAAAAGTGGGGG	54778
rs374174133	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58995336	TTAATACAGAATTGT[A/G]TGTTTCCTGTTTTAT	54778
rs374198853	in-del	-/GTG			intron-variant	RNF111	GRCh38.p7	15:59013848	GGCTGGAGTATAGTG[-/GTG]CTTTCTTGGCTCACT	54778
rs374249787	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59035626	GCTCTGCTTCCTCTC[A/G]AATGGTTTGCTCTTA	54778
rs374258207	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022152	AGCATGAGCCACCAC[A/G]CCTGGCCAAGCTTCC	54778
rs374259381	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59090344	AAGCAATTCTCCTGC[C/G]TCGGCTTCCTGAGTA	54778
rs374289514	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59085567	AGTTAAGAAACCTTA[A/G]ATTACTTTTTTAAGT	54778
rs374341831	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59071627	TTGAGCCTAGGAGGT[A/G]GAGCTTGCAGTGAGC	54778
rs374364576	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59034178	CATTCTTCTTGACAT[C/T]TGCATAGTATTCCCT	54778
rs374426980	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59092962	CTTTGAGCACACCAC[A/C]CTGCACTCCAGCCTG	54778
rs374436217	snp	C/T	0.00438332	0.0466095	intron-variant	RNF111	GRCh38.p7	15:59036352	AGGTTTGAGCCACCG[C/T]ACCCGGCCAAGACTG	54778
rs374450540	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59035053	TGAATGAAGAGCAAA[A/G]TCACGTCTTACATGG	54778
rs374457484	snp	G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59088527	AAAGCTATAAATTCT[G/T]CTTAAAGTATGTTGT	54778
rs374463097	in-del	-/TG			intron-variant	RNF111	GRCh38.p7	15:58997902	TTTTGTTTTTCTTTT[-/TG]TTTGTTTTTTGTTTT	54778
rs374478411	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59024460	GGCTAGCAAGATCTT[A/T]TCAGCAAGTACTTTA	54778
rs374489118	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59070545	CATTATTCTTAAACC[A/G]TATTTACCTGCATTG	54778
rs374498644	snp	C/G	0.000153988	0.00877327	missense	RNF111	GRCh38.p7	15:59058430	ATTAACAATTCAAAT[C/G]CATCTACCTCTGAGC	54778
rs374535995	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59051640	CTGGTGTGGTGGTGC[A/G]TGCCTGTAGTCCCAG	54778
rs374621809	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59014691	TGCAGAAAGAAAGCA[C/T]GTTATCAGGAAAACT	54778
rs374626414	snp	A/T	1.65894e-05	0.00288	intron-variant	RNF111	GRCh38.p7	15:59076228	CTTGTAAGTATATAC[A/T]TAGTGGACACAAAAT	54778
rs374668534	snp	A/G	9.67758e-05	0.00695547	intron-variant	RNF111	GRCh38.p7	15:59055649	AAAAATTCTTTATTT[A/G]TATTTACTAACTTAA	54778
rs374715690	in-del	-/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59017669	TTGAAGCTTTGAAAG[-/T]TTGACAGATTTATTA	54778
rs374785194	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58995916	GCAATCCAATTTGCT[A/G]TTGTGTTATTTATAT	54778
rs374798237	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59013468	CCCTGAATCTAGGTT[A/G]GTGGAATGTTTTTCT	54778
rs374801944	snp	A/C	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59027554	TTTTTTGGGAGACAG[A/C]GTCTTGCTCTGTTGC	54778
rs374804226	snp	C/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59051219	AGCACTTTGGGAGGC[C/T]GAGGAGGGTGGATCA	54778
rs374806764	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59006988	AAATGGGGTTTCACC[A/G]TCTTGGCCAGGCTGG	54778
rs374832839	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59087723	AAGGAGGGATTCATC[G/T]TGCTGTCTCTGGGGT	54778
rs374906990	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59019571	CATTCTTGTCAGGCT[G/T]AATACCTTGGAATAA	54778
rs374917547	snp	C/T	1.6477e-05	0.00287024	synonymous-codon	RNF111	GRCh38.p7	15:59076040	TGCATTTGACCCCTG[C/T]TGCCCTGTTTCTTCC	54778
rs374940878	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59011997	TGTTCTTTTTTGTTT[G/T]TTTGCCTTTTTTTTT	54778
rs374945463	snp	C/G			downstream-variant-500B	RNF111	GRCh38.p7	15:59097520	CGTTTTTCTTACTCT[C/G]GTGACTTTATTTTAG	54778
rs374954455	snp	C/G	3.30333e-05	0.00406393	missense	RNF111	GRCh38.p7	15:59085758	TCCTCGACTTCATCA[C/G]TTACAATTAGGAGCT	54778
rs374990684	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59012437	GTAGGTTTTCTTTAC[A/G]CTTTATGTCACAAAA	54778
rs374995639	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	RNF111	GRCh38.p7	15:59095182	AGTTTAGGGTCACAA[A/G]CCCATAATATGTGCA	54778
rs375033655	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59045772	AAAGTCAATGGTTAG[C/G]TGGATTAATATCTCA	54778
rs375036159	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59063816	AGAGTCAACGTAATC[C/T]TCAAATAACTTGGTT	54778
rs375100763	snp	C/T	0.000153988	0.00877327	intron-variant	RNF111	GRCh38.p7	15:59080913	GGTGCCTATGTAACA[C/T]ACTCAAAATATTTTT	54778
rs375108385	snp	A/C	4.94214e-05	0.00497074	missense	RNF111	GRCh38.p7	15:59066961	CACCACCACCATACT[A/C]CCCACCCAGCTGTCC	54778
rs375148533	in-del	-/GTT			intron-variant	RNF111	GRCh38.p7	15:59072823	CCACTTTTGCTGCAG[-/GTT]TTTTTTGTTTGTTTG	54778
rs375157411	snp	G/T	0.000153988	0.00877327	missense	RNF111	GRCh38.p7	15:59075962	TATCTAGCAGGCATT[G/T]CCAGTGGACCTGAGC	54778
rs375173509	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59090499	CCTCCCAAAGTACTG[C/G]GATTACAGGCGCAAG	54778
rs375198191	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59046118	AGTAATTTTTAAAAC[A/G]TTTCTGTAAATCAGA	54778
rs375221862	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59068879	CAGGAGTTCGAGACC[A/G]GCCTGACCAACATGG	54778
rs375247854	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:58996486	CTTGGGTGGCTGGAG[C/G]AGGAGAATCGCTTGA	54778
rs375270334	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59014928	CCCCTAATTTTTGTA[C/T]TTTTTTAGAGACAGA	54778
rs375277752	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59013158	CCTAGGGATCAGGGG[A/T]AGTTTGTAAATAATA	54778
rs375305172	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59026925	CCACCCCCCCTTGCT[C/G]TCCTCTACCCTTGTC	54778
rs375362809	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59035257	GGGTAGGGATACAGC[C/T]AGACCATATCATTCT	54778
rs375372468	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59050234	CATGCTCGACTAATT[A/G]TTGTATGAGCAGTAG	54778
rs375390524	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59045063	TTATATAAATTGAAT[G/T]TTCATGCATTAGCAA	54778
rs375427661	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59072012	AATTTAAAAATACTT[C/G]AGTTTAAAAATACCT	54778
rs375439852	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59048207	ACTGAGCAAAACCCA[A/C]ATGTCCATCAGTGGA	54778
rs375457805	snp	C/G	0.000297432	0.0121913	synonymous-codon	RNF111	GRCh38.p7	15:59076211	ACATTACATGCCACC[C/G]CCTTGTAAGTATATA	54778
rs375465896	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59053576	ATGGAAGTGAGCATT[C/T]TATAACATATACTTG	54778
rs375493363	snp	A/G	9.89642e-05	0.00703365	synonymous-codon	RNF111	GRCh38.p7	15:59076190	GCCCTCTCTCTCATC[A/G]TGTCGACATTACATG	54778
rs375494502	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59084357	GAAGGATGATGTGGA[A/G]AAACCTAATCCCCAG	54778
rs375588442	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59093273	GGTCCTAGAAAGTTA[C/T]AATGTGTTCTTCAAA	54778
rs375633343	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59022671	TAGGTTGTTTAACCT[C/T]TTCACACTCCATATA	54778
rs375679171	snp	C/T	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:58996495	CTGGAGCAGGAGAAT[C/T]GCTTGAACCTGGGAG	54778
rs375703212	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:58990161	GAGTTTATTGTTAAC[C/G]CTCCTTGGGCTTCAG	54778
rs375736416	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59064871	GAGAGGGCAGAGCCA[G/T]GAGAATTTTAGGGAA	54778
rs375767362	snp	G/T			upstream-variant-2KB	RNF111	GRCh38.p7	15:58987167	TGTTATCTACTGACT[G/T]TTATAAAATAAACAA	54778
rs375807718	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58997967	TGGAGTGCAGTGGGG[C/T]GATCCTGGCTCACTG	54778
rs375831685	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:58993715	AAGGGCAGGCTCTTA[A/C]CACCTGCCTGAAGGG	54778
rs375859811	snp	C/G	0.000105162	0.0072505	intron-variant	RNF111	GRCh38.p7	15:59066740	CATGATTTGATTATT[C/G]TGTGCATTTTTTTCT	54778
rs375866185	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59028047	GGCCAGGCTGGCCTC[A/G]AACTCCTGACCTCAG	54778
rs375914252	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59042922	GGGGTGGGGAGGTCT[A/G]TGATGGTATTTTTAT	54778
rs375954633	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59077413	AAAAGCTTCCTCGCA[C/T]AGCTTACTAATCTTA	54778
rs375963714	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59062295	CAATTCACTTGCCTC[A/T]GCTTTCCAAAGTGTT	54778
rs375984147	snp	C/G			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021084	TTTCCACCCTTTCCC[C/G]CAAAGTCCTTTGTAT	54778
rs376019814	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59012353	CCACTTAGGTAATTA[C/G]AGTATTTGATAATTA	54778
rs376025450	snp	A/G	0.0023933	0.0345097	utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58987686	GCTCTCCTCGGTAGG[A/G]GAGGAATTGGTTAGG	54778
rs376029589	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59006072	TTATCTCCAGTAGGC[A/G]TGGTCATTGTCAAGA	54778
rs376094869	snp	C/T	0.000234051	0.0108153	intron-variant	RNF111	GRCh38.p7	15:59084096	CAATTATTCAATTAT[C/T]TCCAGTGGTCTTTTT	54778
rs376099345	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59084774	TTCCTCATTCATGAC[C/T]CCCCACCCTCTCCCC	54778
rs376106481	snp	A/G	0.000854186	0.0206486	intron-variant	RNF111	GRCh38.p7	15:59030795	TAAATATCTAATTTT[A/G]TCTTCTAGGCTTTCC	54778
rs376128947	snp	C/G	3.2975e-05	0.00406035	missense	RNF111	GRCh38.p7	15:59031020	GAATGAATTCTCTCA[C/G]CTGTGTGATGATTCT	54778
rs376180286	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59082862	TGCCATTCTAATATA[A/G]TAACCTTTTATATAG	54778
rs376220625	snp	C/T	3.31186e-05	0.00406918	intron-variant	RNF111	GRCh38.p7	15:59094732	AATTTGTTAACTACG[C/T]ACAATTATCATAAAA	54778
rs376241962	snp	C/G	1.88386e-05	0.00306903	intron-variant	RNF111	GRCh38.p7	15:59055884	AAAATTATGAAAGGA[C/G]TTTGATAAAAGGAAA	54778
rs376282629	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59059299	CAAATGAAAACCACA[A/G]TGAGATACCACTTTG	54778
rs376290968	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59020185	TAATATGCAAATATA[C/G]TATATATTTTGTAAG	54778
rs376295926	snp	A/C	0.000149884	0.0086556	missense	RNF111	GRCh38.p7	15:59031678	GCCAGTGAAAACCAC[A/C]AAAACAATCCAGCTG	54778
rs376354863	in-del	-/TA			intron-variant	RNF111	GRCh38.p7	15:59011959	CAAAGATTCCTAGCT[-/TA]TATATAAGAATAAGT	54778
rs376422966	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59032587	CCACCACACCTGGCT[C/T]ATTTTTGTATTTTTT	54778
rs376450850	snp	C/G	1.65976e-05	0.00288072	missense	RNF111	GRCh38.p7	15:59052426	AACAGTTGGAGAAAG[C/G]TATCGGTGAGATTTT	54778
rs376462759	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:58990459	GAGGTGACCAGTCTG[A/G]CCAAAATGGTGAAAC	54778
rs376466499	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59010479	TGATCTCAGCTCACT[C/G]CAACCATTGCCTCCT	54778
rs376497752	snp	C/T	8.24029e-05	0.00641831	missense	RNF111	GRCh38.p7	15:59058389	CCACTTCTGCAAGAA[C/T]GGAATCACAAGCTAC	54778
rs376504634	snp	A/G	4.9611e-05	0.00498026	intron-variant	RNF111	GRCh38.p7	15:59085632	GAGACCCTAAGGAGG[A/G]TTAAACTGTTCTCAT	54778
rs376525658	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59081713	GTAGAGCAAGACCCT[A/G]TGTCCTTTAACAACA	54778
rs376586350	snp	A/G	0.000148394	0.00861248	missense	RNF111	GRCh38.p7	15:59081247	GAAGTGATGCAGAGG[A/G]TGGAAGTTCAAAGGA	54778
rs376591728	in-del	-/GA			intron-variant	RNF111	GRCh38.p7	15:59049361	AGTCCAGGTGTCTTT[-/GA]TTTTTTTTTTTTTTT	54778
rs376593171	snp	C/T	0.000153988	0.00877327	synonymous-codon	RNF111	GRCh38.p7	15:59031275	TTTTGGAGATTCTGA[C/T]ACTGTGACTTCAGAT	54778
rs376600174	snp	C/T	1.64738e-05	0.00286995	missense	RNF111	GRCh38.p7	15:59081091	TCTTCTCATGCAACA[C/T]CTCATCCTGTGGCAC	54778
rs376671663	snp	G/T			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986730	ATGTTGGCCAGGCTG[G/T]TCTTGAACTCCTGAT	54778
rs376679236	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59029096	GTATTTAATTTTTGA[C/G]GATCTGCTAGACCGC	54778
rs376695089	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59067242	CCTCCCTCCGTTTCC[-/T]TTTTTTTTTTTTAAC	54778
rs376699470	snp	C/G	0.000153988	0.00877327	intron-variant	RNF111	GRCh38.p7	15:59080915	TGCCTATGTAACATA[C/G]TCAAAATATTTTTCT	54778
rs376720970	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:58990053	CTTGACATTACCGTT[C/G]TATGGGTAACGTTAT	54778
rs376766435	snp	A/T	0.000153988	0.00877327	synonymous-codon	RNF111	GRCh38.p7	15:59084222	TCAGACTATGTCCTC[A/T]CATCCTCGACAGGCT	54778
rs376816195	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59010637	GAACTCCTGACATCA[C/G]GTGATCTGCCCACTT	54778
rs376873248	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59042134	TGCCAAATTTTTTTT[-/T]CTTTTTTTGAGACAG	54778
rs376895017	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59073166	CAACACAGTGAGACC[C/T]TGTCTCAAAAGTAAA	54778
rs376895453	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59079913	AAATGTTTACACCCT[A/T]TTATGACAGAGCTTC	54778
rs376897378	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59038041	TAACTTATTTACATA[C/T]AAGATATTGAAAAAA	54778
rs376903487	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59058050	TTATTTCCTTTTACT[A/G]TTTTCTTCTTTGTGA	54778
rs376921629	in-del	-/C			intron-variant	RNF111	GRCh38.p7	15:59025736	TGGCTTTTTTTTTTT[-/C]TTTTTTCTTTTGTGT	54778
rs376941290	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59038661	TTTCACAAAAATTGT[A/T]GACATCATTTTACTC	54778
rs377010430	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59017184	AAAAATTGTCTTCTA[C/T]GAATCCGTTCCCTGG	54778
rs377013840	snp	A/C/G/T	0.00101814	0.0225413	intron-variant	RNF111	GRCh38.p7	15:59075939	AAAGATAAAATATAC[A/C/G/T]TCCTTTTTATCTAGC	54778
rs377019284	snp	A/G	8.23879e-05	0.00641772	missense	RNF111	GRCh38.p7	15:59076129	CATCAATAGATGGCT[A/G]TGGATCAAGCATGGT	54778
rs377064935	snp	A/G	6.6855e-05	0.00578126	synonymous-codon	RNF111	GRCh38.p7	15:59030870	CTACACCTTAAAAGT[A/G]GATATGAAGAGTGAG	54778
rs377105852	snp	A/C/G			intron-variant	RNF111	GRCh38.p7	15:58990523	AGCTTAGTGGTGTGC[A/C/G]CCTGTAGTCCCAGCT	54778
rs377131377	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59094369	GAGAGAATTAAATGA[C/T]GTAATAAATATATAT	54778
rs377136049	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59086586	GGGAATAGTTTTGTG[G/T]TGTTGTGGGTAGAGG	54778
rs377167815	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59056111	GGTTAGCTCAAACTA[G/T]TTTAGTTTGATTTGT	54778
rs377284860	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59008846	CATCTTTGTCACAGT[C/G]TTTCTTCAAGGAATA	54778
rs377341631	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59011986	CTTAATTTTAGTGTT[C/T]TTTTTTGTTTGTTTG	54778
rs377350147	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59033452	CAGGTGAGAGGAGTG[C/T]AGAATAACCATTGCC	54778
rs377361399	snp	A/C/G	1.65004e-05	0.00287227	missense	RNF111	GRCh38.p7	15:59076195	CTCTCTCATCATGTC[A/C/G]ACATTACATGCCACC	54778
rs377385476	snp	C/T	8.87036e-05	0.00665912	intron-variant	RNF111	GRCh38.p7	15:59067131	GCCCCTCTTGTCTCT[C/T]TCTCTCTCTCCTTCT	54778
rs377393383	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59011884	TTGGCATATGTTCCA[A/G]CTGAAGATAATGTCT	54778
rs377433161	snp	G/T			upstream-variant-2KB	RNF111	GRCh38.p7	15:58985940	GCCACATATGGCTGG[G/T]GTCTACCTAATTGAA	54778
rs377504915	in-del	-/GTTTGTTTGCC			intron-variant	RNF111	GRCh38.p7	15:59011993	TTAGTGTTCTTTTTT[-/GTTTGTTTGCC]TTTTTTTTTTTTTTT	54778
rs377569297	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59068525	CAGGATAATCACTTT[-/T]AACTTTAGAGGTGGA	54778
rs377656786	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59023761	TTAATGAGAATGCCT[A/G]TAGTGTTTCACTATT	54778
rs377673582	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59071664	TGTGCCACTGCACTC[C/T]AGCCTGGGTAACAGA	54778
rs377676482	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59054962	ACATATTATCCCTGT[A/G]TGTCCTTAGTCCAAA	54778
rs377686408	in-del	-/G			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:58988087	AGGGGAACGGGGGGG[-/G]AGGGGATCCATTGGA	54778
rs377707346	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59028839	AGCTGGACTGTAGCG[A/G]TGCAGTCCCAGCTCA	54778
rs377717903	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59058811	ACACCAAAAGCATGA[A/G]CAACAAAAGCAAAAG	54778
rs377718316	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59014016	GGCTGGTCTTGAACT[A/C]CTGAGCTTAGGCAAT	54778
rs377719734	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59029992	TCATTTTGAGTCATG[A/G]TATTTACTATTACAT	54778
rs377723093	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59090391	CCCGCCACCACGCCC[A/G]GCTAATTTTTGTATT	54778
rs377734047	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59086068	TATACTGTGCTTCAG[G/T]TATTTTGCCGTAAGT	54778
rs386383154	in-del	-/TA			intron-variant	RNF111	GRCh38.p7	15:59016173	TATGTATATATATAT[-/TA]AGTTTTTTTTTTTTA	54778
rs386383156	in-del	-/TT			intron-variant	RNF111	GRCh38.p7	15:59062052	TTGTTTTAAACTTCT[-/TT]TTTTTTTTTTTTTTT	54778
rs386784464	in-del	CT/TAA			intron-variant	RNF111	GRCh38.p7	15:59053879	ATCTCTTATTGTTAT[CT/TAA]GAGATATTAATTTTG	54778
rs386784465	in-del	AA/TAACTCC			intron-variant	RNF111	GRCh38.p7	15:59067254	TCCTTTTTTTTTTTT[AA/TAACTCC]CTCCCATTCTTCCTT	54778
rs386784466	multinucleotide-polymorphism	GGT/TGC			intron-variant	RNF111	GRCh38.p7	15:59079829	GATGGGAAACAAATA[GGT/TGC]CTCCTTCACCTTAAT	54778
rs397697883	in-del	-/A	0.375	0.216506	intron-variant	RNF111	GRCh38.p7	15:58989885	TCTTTAAACTATAAC[-/A]AAAAAAAAAAGAAGG	54778
rs397710077	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59083154	GCTTAAAAAAAAAAA[-/A]GAAGCAAAAAATGAA	54778
rs397710433	in-del	-/A	0	0	intron-variant	RNF111	GRCh38.p7	15:59026732	TTTTAGAAAAAAAAA[-/A]TTTAGAACATGATAC	54778
rs397779758	in-del	-/T	0.375	0.216506	intron-variant	RNF111	GRCh38.p7	15:58997532	CATACCCAGCCCTGA[-/T]TTTTTTTTTTTTTTT	54778
rs397820174	in-del	-/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59045179	ACAGTTTTTTTTTTT[-/T]AAGTGTTTCCTCTTT	54778
rs397837030	in-del	-/TA			intron-variant	RNF111	GRCh38.p7	15:59023539	TTATTTTTATTTATA[-/TA]TTTTTGGTAAATATA	54778
rs397853868	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59069074	ACAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	54778
rs397946700	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59024525	AGAGGGTGATTTTTT[-/T]AAAGTGTGTTTTAGT	54778
rs398027504	in-del	-/A	0	0	intron-variant	RNF111	GRCh38.p7	15:59046197	CAAAAAATTAAAGGG[-/A]AAAAAAAAAAAAAGC	54778
rs398043364	in-del	-/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:58995477	TTGTTTTTTTTTTTT[-/T]GACGGAGTCTCACTC	54778
rs398043367	in-del	-/C	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59093363	TTTTTTTTTTTTTCC[-/C]TTTTCTGGGAGATGG	54778
rs527252263	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59092107	TATTTTCAAAGAGTA[C/T]TGAGGTATTACCAGT	54778
rs527253609	snp	C/T	0.00478085	0.0486577	intron-variant	RNF111	GRCh38.p7	15:59084820	ACATGCTACTCTCTC[C/T]TGTGAGTTTAGGTTT	54778
rs527341159	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59085953	TGTATTAAAATCTGC[A/T]CGTATAATTTGCATC	54778
rs527349648	snp	A/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59054180	CTGACCTTGTGATCC[A/G]CCCGCCTCGGCCTCC	54778
rs527364795	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59091441	TATATATTTTTGTCT[A/G]CTTTAAAAAAAACAC	54778
rs527386741	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59011596	GAGGCCCCTCTTCTT[A/G]GTTTATAAATGATCG	54778
rs527395961	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59018055	TGAGGCACCACGCCC[A/G]GCCTATTTGTTGAGC	54778
rs527442808	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58993539	TGAGACTCCATCTCA[A/G]AATTTGTGAAAGTAC	54778
rs527459621	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59053930	TTTGCCCTTTAGTTT[A/G]TTTTACTTAATTATT	54778
rs527465373	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59023188	GGGAGGCGTAGGTTG[C/T]AGTGAGCTGAGATCA	54778
rs527469081	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59070489	TTAGTCTAAATAGTA[A/G]GGAAAGGATTTGAAC	54778
rs527470630	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59017626	CAGGAAGTTAAAATA[A/G]CAGAAATCTCTAAGA	54778
rs527473733	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59060001	ATCAGGAAGTATTCT[C/G]TCCCCTGGAAAACTG	54778
rs527489029	snp	A/G			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021609	TCATTTAACCGTTAC[A/G]GAATTTTATGAGGTA	54778
rs527490400	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59047895	ATTTTAGAAATGGTT[A/G]TTAAAACCACAATGA	54778
rs527493514	snp	C/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:58988132	GCAACGGGGGAGGGG[C/T]CGGCCTGGAGGGGAG	54778
rs527510855	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59029902	TGTTAAAAATATGTT[A/G]ACATTGTTTATTCAT	54778
rs527537781	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59065498	TTATTACCACATTTT[A/T]TAGATGAAAAGGAGG	54778
rs527594483	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59029155	TTTCCATCAGCAATA[C/T]ATGAGGGTTCCAATG	54778
rs527621325	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58999460	GCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA	54778
rs527662120	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59065195	TAAGGATGGCAGCAG[A/G]GCGGGGCTTTGGCTT	54778
rs527696080	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59041310	CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG	54778
rs527700505	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58992234	ATTTTTAGTAGAAAC[A/G]GTTTTTCACCATGTT	54778
rs527725298	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59051436	GCACTCCAGACTGGG[C/T]GATTGAGCGAGACTC	54778
rs527737667	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58998874	TTGAAAGAGGTGCGT[A/G]ACTTGGTGAAACAAT	54778
rs527854000	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59010370	TTGATAGATGACAGA[C/T]GGATTCCACATCTGT	54778
rs527858186	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59089925	ATTTGTAAGTATTAT[C/T]AATCTTAGGGTCAAA	54778
rs527882684	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59046277	GGGGTCCCTGCAGCC[G/T]CAGCCTCCAGGGCTA	54778
rs527937415	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59053284	TCCAAAATATCAACT[C/T]CTAACATTGCATTCA	54778
rs527954803	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59052740	TTCAAAGCAGGCTGC[A/G]TTAAACTCACCTGGA	54778
rs527964006	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59089171	TTAGCCTGTGGGTCA[G/T]TTCACACATATGTAA	54778
rs527979339	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021402	TTCATCCGCCTGTCT[C/T]GGCCTCCCAAAGTGT	54778
rs527987642	snp	G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59016237	TGCAGTGGCATGATT[G/T]TGGCTCACTGCAACC	54778
rs528070424	snp	A/G	3.29571e-05	0.00405924	synonymous-codon	RNF111	GRCh38.p7	15:59058399	AAGAATGGAATCACA[A/G]GCTACTAGCGCTTCC	54778
rs528078092	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022048	TATTTTTAGTTGAGA[C/T]GGGGTATCACCATGT	54778
rs528087853	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF111	GRCh38.p7	15:58986142	TTTAGTTTTCCCACA[C/T]AATCTGCTATCCTTG	54778
rs528100199	snp	A/G	0.000236379	0.0108689	intron-variant	RNF111	GRCh38.p7	15:59093491	GCTGGGATTACAGGC[A/G]TAAGCCACTGCACTC	54778
rs528129177	snp	A/G	0	0	intron-variant	RNF111	GRCh38.p7	15:59063879	CATGAAGGTAATTTA[A/G]CGTATCCCAGTGAGT	54778
rs528130116	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59064273	GGGCGTGGTGCCTCA[C/T]GCCTGTAATCCCAGC	54778
rs528142998	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59070566	ACCTGCATTGAAGAC[A/G]TACATTGTATTTGCC	54778
rs528161777	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58991517	AAGTGCCATGAGGAA[A/G/T]ATAGGACCATGTGAT	54778
rs528199609	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:58991084	GTAGATCATGAGGTC[A/G]GGTTCGAGAGCAGCC	54778
rs528210018	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59034041	TCTTCTTCAGATCCT[C/T]CAGTGTTACTATTAA	54778
rs528265716	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59018161	TTTGATAAATTATTA[A/T]CATTTTCGAGCATTA	54778
rs528300159	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59039302	TGCTTAGGTTTATTA[C/T]CTGAGGTTCTTCTAT	54778
rs528302329	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58997497	ATCACTATGTTCTTC[A/G]TGACTACACATTTGC	54778
rs528338440	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59030747	TGAGAACTCTTCAAT[G/T]AAATAGTATAATAAA	54778
rs528341221	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59002963	CCTGTTGATGGTCAA[C/T]CTTTACATTTGTTTT	54778
rs528447290	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59087734	CATCTTGCTGTCTCT[G/T]GGGTGGCAGAGGTGG	54778
rs528449344	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF111	GRCh38.p7	15:59004056	TTTATCCTCCTTGCC[A/G]TAGCTGAGTTGATCT	54778
rs528485914	snp	C/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59028261	TATCTTTTTGACTGG[C/T]TTCTTTTACTTAGCA	54778
rs528512604	snp	A/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59051232	GCTGAGGAGGGTGGA[A/T]CATGAGGTCAGGAGA	54778
rs528526165	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59057053	TCTAAAACTAAGTAC[A/G]TCAGACCAGTGGTTC	54778
rs528547202	in-del	-/TTAA	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59009999	TTGCTAAATTGTAAG[-/TTAA]TTATTTTCAGGTTCT	54778
rs528586297	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59056641	CAGCTCTTCTATGGG[C/T]TATTTGCAGTTTGGG	54778
rs528589355	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59011567	TTAAGGTATCAGCAG[G/T]TTTGGTTTTTCCTGA	54778
rs528606125	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59062749	CAAGGTTATATGATA[C/G]TGGAGCAAGAATTCA	54778
rs528620912	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59007098	GTAAACTTTACATAC[A/G]GTGAAATGCACAAAT	54778
rs528677250	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59050513	CCCTGACACTAGACT[C/G]TATATCAAAGGGGTT	54778
rs528685853	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59085893	TTTTAATAGAATTTG[A/G]GAGTAATCTTGTTAG	54778
rs528708681	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59026188	GTAGAGTTCCTCAGA[A/G]TTGTATGGATAGTCT	54778
rs528712964	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59062212	CACACCTGGCCAATT[C/T]ATGTATTTTTTGTAG	54778
rs528802278	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59074308	GCCAGCCATTGACTT[C/G]TCTTTGCTATGAAAG	54778
rs528814698	in-del	-/TTT	0.0103295	0.0711199	intron-variant	RNF111	GRCh38.p7	15:59090242	TGTTTGTTGTTGTTG[-/TTT]TTTTAGATGGAGTCT	54778
rs528820431	snp	G/T	0	0	intron-variant	RNF111	GRCh38.p7	15:58989948	ACTTATGTGCCCTTC[G/T]TTTGACTTTTTCTCC	54778
rs528839203	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59053529	TGCTTTTCCACTTGC[C/T]ATTTTAGCATCGAAG	54778
rs528854418	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59038116	AATTTTATTCACACA[A/G]CCATCGTAGACCTTG	54778
rs528861440	snp	A/C			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020780	CTACCAAACTCCAGT[A/C]CTCCATAATAGAGGA	54778
rs528868521	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59037635	TGAGGTCTGGAGTTC[A/G]AGACCAGCCTGACCA	54778
rs528910487	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58995353	GTTTCCTGTTTTATT[C/T]AGTGGGTTAAATAAC	54778
rs528933638	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59001249	GGAGAATGGTGGTCT[C/T]TGAGAACAGAGGTAT	54778
rs528955857	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59043100	GGTATAATTAACTAC[C/T]ATAAAATTCATTTTA	54778
rs528963735	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59086642	CTTTCTGGTACATGT[G/T]ACTTCTAAGCAGACT	54778
rs528964820	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59060173	CCACTGTACCCAGGG[G/T]TGTCTTTTAAAAACA	54778
rs528991728	snp	A/G	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59080160	GAGTCTCACTCTGTC[A/G]CCCAGGCTGGGGTGC	54778
rs528994551	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59007394	TAATCCGTATTGATA[A/C]ATGTATCAGTAGTTC	54778
rs529032277	snp	G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59013478	AGGTTAGTGGAATGT[G/T]TTTCTCATAGTTTGG	54778
rs529033928	snp	C/T	0.0111196	0.0737302	intron-variant	RNF111	GRCh38.p7	15:59047418	CAGGATTGCTTGAGC[C/T]CGGGAGGTCAAGGCT	54778
rs529048915	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59093167	AATATACTGCCTATT[A/G]TAGGGCCACACAAGG	54778
rs529079259	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59040649	ATATGCCATAAATAC[A/C/G]TACACATAAGTGAAC	54778
rs529094468	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59032072	GCCTCCCAAGTAGCC[A/G]GGATTACAGGTGCCC	54778
rs529117522	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59065373	TGCAGTTCTTCTGCC[A/G]TAGAAGAACATACCT	54778
rs529135580	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59049311	GCTTATTTCACTTAG[C/T]GTAATGCCCTCAAGT	54778
rs529140398	in-del	-/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59015239	TAAGATAGAAGTCAC[-/T]TATGTTTTCCTTATC	54778
rs529154175	snp	A/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59019139	TAGAGGTGAGGTTTC[A/T]TGTTGCCCAGGGTGG	54778
rs529158753	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59061286	ACCCTATGGAACATT[A/G]GTTCAACTATGTTCT	54778
rs529252267	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58988911	TTTTGTAGGATTTCC[G/T]GTAGCTTTTGAATGT	54778
rs529335241	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF111	GRCh38.p7	15:58988298	CAGCCTACAGTGAGG[G/T]AGTGTGGGTGAGGGG	54778
rs529345547	snp	G/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:58994331	GGCGTGAGCCACCAC[G/T]CCTGGCTACTTACAT	54778
rs529353686	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59079399	AACAGAACTTTTAGA[A/G]AATTGGTTTAAAAAT	54778
rs529405310	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59030096	ATGTTGAATGATTTA[A/G]ATAGATTAGCTGTAC	54778
rs529417061	snp	A/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59078789	GCTTGAACCTGGGAG[A/T]TGGAGATTGCAGTGA	54778
rs529454442	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59013257	GAGTTCCCATATATC[A/G]CTCACTCAGTTACCC	54778
rs529459179	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59017438	GTTTAATTTTACATT[C/T]ACCTGTTACAGATTG	54778
rs529466486	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59010708	CATCTGACCTCCACA[A/T]CTGTTTTAATCTTTG	54778
rs529520484	snp	A/T	0.00557542	0.0525036	intron-variant	RNF111	GRCh38.p7	15:59041962	ATCAGTCTGTTCATA[A/T]TTTTTTTTTTTTTTT	54778
rs529524510	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59084747	TTGTACCCATCGACC[A/G]GCATCTCCCCTTTCC	54778
rs529529999	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59048132	GAGAAATGAAAGCAC[A/G]TGTTTGTAGGAAGAC	54778
rs529583035	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59041488	AACCCAGGAGGCGGA[A/G]GTTGCAGTGAGCCGA	54778
rs529587381	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59084444	CTGGGGCAGGGAACC[A/G/T]TATCAAGCAGGAGTA	54778
rs529602574	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59091340	TCTGCAGACCCTAGT[C/T]CTTCTTCCCAGAAGT	54778
rs529623429	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59054136	TAGAGACGGGGTTTC[A/G]GCATATTAGCCAGGC	54778
rs529639443	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59005468	GCAGTTTTGCTCCCA[A/G]CATTAGATCCCGCAT	54778
rs529647423	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59090586	TTGTGACTTAGAACT[A/G]TTGTTTGATTTGGTT	54778
rs529661530	in-del	-/TGTT			intron-variant	RNF111	GRCh38.p7	15:59090231	GTTTGTTTGTTTGTT[-/TGTT]GTTGTTGTTTTTTTA	54778
rs529694731	snp	A/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:58999799	CCATAGGTTTTATAG[A/G]AAGCGTGGCAGCATC	54778
rs529698804	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59011528	CTTTACTTACTCCTA[C/G]TTCTGTAGAGTGTAA	54778
rs529756737	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59023386	TGTTTTCATGTAGGT[C/T]CTTTGTGTCTCTTGT	54778
rs529759156	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59065460	GAGAAATTTATCTTT[C/T]CTAACAACCATGCAA	54778
rs529763421	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59059160	AACAAACAAAAAGCC[C/T]CAACCCAACAGAAAG	54778
rs529804423	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59026606	AAATAATTTAGAATA[-/T]TATCTGTTATATTTG	54778
rs529813886	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59001432	TTTTTGTTGTTGATT[-/A]AAAAAAAATTCTTTT	54778
rs529815971	snp	A/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58987678	AGTGTCGTGCTCTCC[A/T]CGGTAGGGGAGGAAT	54778
rs529870482	snp	C/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59064922	CAGAGCCTGAAGCAC[C/T]CCCCTACCCAGGTTC	54778
rs529901828	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF111	GRCh38.p7	15:58987226	TTCGCAGGAGATATG[C/T]GACCACTTTTGATCT	54778
rs529905739	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58999845	CTCTGAGCTTTTACT[C/T]ATGGTAGAGGGCAAA	54778
rs529996732	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59071248	AGCTTGCAGTGAGCC[A/G]AGATTGCACCACTGC	54778
rs530012412	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59048122	ATTTACCTAAGAGAA[A/T]TGAAAGCACATGTTT	54778
rs530012888	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58992159	AAGCAATTCTTCTGC[A/G]TCAGTCTCCTGAGTA	54778
rs530032557	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59040294	TAATTTTTAAATTAT[A/G]TTTTAATTTTTTTTT	54778
rs530044160	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59039904	TGTGTTTTAGTAGAG[A/C/T]CGGGGTTTCACCGTG	54778
rs530047610	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59046842	AAAAGACTTGTATTC[A/G]GGATATATAAGGAAC	54778
rs530171640	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59003737	TTTCGCTCTAAAATT[A/G]TCTTGGTTTTTTGGT	54778
rs530175485	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59049903	CGTGCCACCACACCC[A/G]GCTAATTTTTGTGTT	54778
rs530197648	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59089830	TATATATATACTACT[A/G]TACACAATTGTGTAG	54778
rs530217671	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59009278	ATTTTACTTTTACAT[A/G]TTATCAGCTTTGGGA	54778
rs530259833	snp	G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59089034	CTCAAATACGGCAGA[G/T]CCCTGTTCTACCTCA	54778
rs530273341	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime	RNF111	GRCh38.p7	15:59097080	TTAATATAGGAGCTT[A/G]TTAAGCTACTGCCAT	54778
rs530274875	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59052084	AACAAATCCATAGAA[C/G]AGGAAGTAAACATGC	54778
rs530296454	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59052602	TTTTTGGTAAGAGAT[A/G]GAATATTGCTATGTT	54778
rs530301835	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021921	GCTGAAGTACAGTGA[C/T]GTGACCTCACCTCAC	54778
rs530304942	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59094634	ATATTATATTGCCCA[C/G]AGTGCTAATTTAATC	54778
rs530374624	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59057803	TACGAAGTATGTGAT[C/G]TCAGTTCATCCTAAT	54778
rs530401084	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59064515	CACTCTAGCCTGGGC[A/G]ACAGAGCAAGACTTT	54778
rs530430841	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59015653	GAACAAAAGAACCTA[C/T]AGCCCCAAGCATTAG	54778
rs530433784	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58991024	GCTGAGGCTGGGTGC[A/G]CTTGCTCATACCTGT	54778
rs530441298	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59063692	CAAAGAGGTTCTGGA[C/G]TATATATATTCAAAA	54778
rs530456619	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59026750	TAGAACATGATACAA[A/T]ACAGCGATGGATTTT	54778
rs530521370	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59027087	TCTTTGTAAATTAAT[A/G]TATGGCTGCATGTTC	54778
rs530530313	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59082103	CCCAAAAAAGTAACT[A/G]TACTAAATCCTCATT	54778
rs530531357	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59075250	ACCTTCAATTTATTA[A/C]AAATAAAACAAAAAA	54778
rs530628413	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59075824	CTGGTTCTTCATACT[A/G]AGAATCTTCCTGGTT	54778
rs530693966	snp	A/T	0	0	intron-variant	RNF111	GRCh38.p7	15:59087686	TTATTGTCTTCACAT[A/T]GAGTAAGCTGAAGAG	54778
rs530755473	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59086854	CCTGATCAAATTTAT[G/T]ATTTTAGAGTTATTT	54778
rs530756852	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59002352	AATAGCTGTCCCTTC[C/T]GTTTTCCCATGGTAT	54778
rs530795605	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59008498	GCTGGTATTTACAGG[C/T]GTGAGCCACCGCACT	54778
rs530796030	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59043861	GGTACCATGGTGTCA[G/T]TTATGAAAAGAATAT	54778
rs530798925	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59010880	ATTCCTTCTCCTGTT[A/G]TTTAATTGGAATGAA	54778
rs530803944	snp	C/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59051206	CGCCTGTAATCCCAG[C/G]ACTTTGGGAGGCTGA	54778
rs530808383	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59000583	GGTATGGTGGCGGGC[A/G]CCTATAATCCTAGCT	54778
rs530873886	snp	G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59061999	ACCTATCACTAGTAT[G/T]CTGATGACTCTCTCT	54778
rs530876743	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	RNF111	GRCh38.p7	15:59094921	TGTTTCAGAACTCTT[A/G]CCCTCCCTCTCATTC	54778
rs530933700	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59068100	TATGATATAAGTCTG[C/T]GTGTTGCAACTCAGG	54778
rs530933906	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59007536	AACATTCATATACAA[A/G]TCTTTGTATTCACGT	54778
rs530995430	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59019771	CGAGACCGGCCTGGC[C/G]AACGTGGTAAAACCC	54778
rs531034117	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59019293	AAAATAATGAGAAAA[C/T]GCAAACAATATTACT	54778
rs531045288	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59067776	TAATTCATGAAAAAT[C/T]GGAAAATTCTCCCAG	54778
rs531064448	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF111	GRCh38.p7	15:58986263	ACTCTGTCGCCCAGG[C/T]TGGAGTGCAGTGGCA	54778
rs531103347	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990240	TTAGGTCCCAAATTT[A/G]ATGGTTTGTATATCT	54778
rs531108419	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59073671	CCCCTCAAAGTGTGC[A/C]TGAGGCTTGGAATCC	54778
rs531121882	snp	C/T	0.0425829	0.139564	intron-variant	RNF111	GRCh38.p7	15:59080114	CCTTCTTGTGTGCTC[C/T]TTTTTTTTTTTTTTT	54778
rs531130556	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59032090	ATTACAGGTGCCCAC[C/T]ACCATGCCCAGCTAA	54778
rs531150342	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59078753	AATCGCAGCTACTCG[G/T]GAGGCTGAGGCAGGA	54778
rs531172480	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59074196	GCATAAATCTTAAGG[A/G]CCCTGGGAATTCTGG	54778
rs531199466	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59043051	AGTTTTGTATCTTGC[A/G]GAGAGCGTTTTATGT	54778
rs531263938	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59001151	GGGAAGAGCATTCAA[A/G]GCAGCGTGACTAGCC	54778
rs531264312	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58994547	CAGCAGTGTGATCTC[A/G]GCTCACTGTAACCTC	54778
rs531298096	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:58999381	CACACTGTCACCCAG[G/T]CTGGAGTGCAGTGGT	54778
rs531330497	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59036989	CAGGTGTGTGCAACT[A/G]CAGTTGACTAATTTT	54778
rs531335271	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59023038	GATCACCTGAGGTCA[C/G]GAGTTCGAGACCAGC	54778
rs531352240	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59000642	TTGAACTGGGAGGCA[G/T]ATGTTTCAGTGAGCC	54778
rs531355143	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59012868	CTCAGCCTCCCAAGT[A/G]TCTGTGATTACAGGT	54778
rs531357531	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59007237	CTTGTCAGTCCTTTC[C/G]CCATCCCTTGAAGAC	54778
rs531412702	snp	C/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59093108	ATCTGGCGAGTGAAA[C/T]AATAAAAGATTAAAG	54778
rs531475209	snp	C/G	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59024544	GTGTGTTTTAGTCCA[C/G]ATTCTCTGAGAAGCA	54778
rs531510006	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59024062	GTTTCTCTCTTTTAA[A/G]GACCTGATTATCCCC	54778
rs531515255	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59037710	GCGTGGTGGCGCATG[C/T]CTGTAATCCCAGCTA	54778
rs531517111	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58998456	CTCATTGTGTCCGTA[C/T]GTTCTTGGGAAGGTT	54778
rs531576241	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59054289	AGTCTTTTGTGTCAG[A/G]ATTTGACAGTTGCTA	54778
rs531588978	snp	C/G	6.58903e-05	0.00573941	missense	RNF111	GRCh38.p7	15:59066919	AGTTGCTTTCAGCAG[C/G]ATGGTCACCATTTTC	54778
rs531592971	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59060014	CTCTCCCCTGGAAAA[A/C]TGAGGGCAGAATTGA	54778
rs531624030	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59036052	AAGACATACCCGAGA[C/G]TGGGTAATTTATTCT	54778
rs531661321	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59066349	GGTGTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	54778
rs531677518	snp	C/T			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020977	GGTTACATGAATAAG[C/T]TCTTTAGTGGTGATT	54778
rs531686992	snp	A/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58999980	AAAGGGATGGTGCTG[A/T]ACCATTAGAAATTGC	54778
rs531711779	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59078698	ACCCTGTCTCTACTA[A/G]AAATTCAAAAACTAG	54778
rs531739525	snp	A/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59084317	AAACTATTGGAAGAG[A/T]TGCCTTGTGATTGAT	54778
rs531809748	snp	C/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59005308	ACAGGCACGAGCCAC[C/T]GCACCCAGCCTCTAG	54778
rs531815135	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58989591	TTGCTAGTTATTTCA[C/T]CAGACATAGAACTGG	54778
rs531826506	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58992895	TTTAGGCTGGACATG[A/G]TGGTGCACACCTGTA	54778
rs531841163	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59072032	TAAAAATACCTTATT[G/T]TACATGTTTCAGTTT	54778
rs531857190	in-del	-/TCCTTCCTTTCCTCTCTTCCCC	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:59067271	ACTCCCTCCCATTCT[-/TCCTTCCTTTCCTCTCTTCCCC]TCCTTCCTTCCCTCT	54778
rs531860341	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59090402	GCCCGGCTAATTTTT[A/G]TATTTTTAGTAGAGA	54778
rs531879565	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59053759	TTTTCCTTGTAGGAC[C/T]AGAGATCTTGTTTTG	54778
rs531881113	snp	A/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59068215	ACAGAGTGAGATGCT[A/G]TCTCAAAAAACAACA	54778
rs531883393	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59067289	TTCCTTTCCTCTCTT[A/C]CCCTCCTTCCTTCCC	54778
rs531897659	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59084360	GGATGATGTGGAGAA[A/T]CCTAATCCCCAGTTT	54778
rs531922188	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59090006	AATATAAAAATGTAT[G/T]AAATCAATATAAATG	54778
rs531932359	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RNF111	GRCh38.p7	15:59097758	GGTAGCGGGTGCCTG[C/T]AGTCCCAGCTACTCA	54778
rs531967109	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59079309	CAATCATAAAACATA[C/G]TGGATTCATTTTTTA	54778
rs532018066	in-del	-/T	0.227074	0.248947	intron-variant	RNF111	GRCh38.p7	15:59051451	GATTGAGCGAGACTC[-/T]TGTCTCAAAAAAAAA	54778
rs532030810	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59064842	AATCCGGAAAGGCAG[C/G]ATAAGACATGTAAGA	54778
rs532092476	snp	A/G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59071155	ACAAAAAAAGTAGCC[A/G/T]GGCGTGGTGGTGGGT	54778
rs532120111	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59016779	CTAGGCCATGTACCA[A/G]TAGGTGAGTGGTGGA	54778
rs532137683	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58992075	TTTTGAGATGGAGTT[G/T]CCCTCGTTGCCCAAG	54778
rs532203163	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59070625	GATTGTACAGCTCAA[C/T]AGAAGGAGAACAGAC	54778
rs532232403	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59077153	AATGGGCCAATTCTT[C/G/T]GTATGAGCACCAGTG	54778
rs532254600	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59028325	TGGTAGTCTGCGCCC[C/T]TGTCCAAGGGGAAAC	54778
rs532256512	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022128	GCCGCCCAAAGTGCT[A/G]GGATTACAAGCATGA	54778
rs532377975	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59082268	TCTTTATGCAAACCA[A/G]TTAAAAAAAAGTACC	54778
rs532425216	in-del	-/TTT			intron-variant	RNF111	GRCh38.p7	15:58994055	TTTTTTTTTTTTTTT[-/TTT]AATGGAGTCTCACTC	54778
rs532425715	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59076663	CCAGGAGTTTGAGAC[C/T]AGCCTAGGCAACATA	54778
rs532437554	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59052009	CAGATATTACAGGAT[A/G]AATATCTATATAAGA	54778
rs532437776	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59082912	TCTTATCTTCCAGTA[A/G]CTGGCAAATTGTTGT	54778
rs532465131	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59039869	CTACAGGCACATGCC[A/G]CCGTGCCCAGCTAAT	54778
rs532490689	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59003717	TATTTTCTTAATAGC[A/G]CGTGTTTCGCTCTAA	54778
rs532502011	snp	C/G/T			intron-variant	RNF111	GRCh38.p7	15:59001737	AACACCTACAAAACA[C/G/T]ACATTATCATGGGAT	54778
rs532524412	snp	A/G	0.00636936	0.0560724	intron-variant	RNF111	GRCh38.p7	15:59088999	CAGTCTGCAAACAAG[A/G]CACTGGTTTATAGTA	54778
rs532582860	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59084869	GTAAGAGGCGTGGAC[C/G]TTTTTTCCTGTTCTT	54778
rs532583004	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59014812	ACCACCTGGAGTGCA[A/G]TGGCACCATCACGGC	54778
rs532628318	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59088488	TGCTTATTTAAATTC[C/T]TTTCCACATATGAAG	54778
rs532639198	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59057197	TGTTGCTAAACATCA[G/T]GCTGTTCACAGTGCA	54778
rs532640017	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59027036	ATGAAATGATGGAAA[A/G]GAAATTGGGTTTAGT	54778
rs532677726	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59026558	ATAATTTTTACAAAA[A/T]TAAAAGACTAGAATA	54778
rs532778763	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59063562	GTGTTTTATTTACTG[A/C]ATCATATATCTCTGT	54778
rs532807682	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990294	TTGTGTTTGTCGTAA[C/T]TGAATCCCCAGAAAG	54778
rs532813954	snp	C/G	0.00318978	0.0398085	utr-variant-3-prime	RNF111	GRCh38.p7	15:59095857	AGATTTGGAATTTAA[C/G]TCACTGGCAGGTATC	54778
rs532820086	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59002302	ACTTTTAAAGATCAA[C/G]TCTTAAACTTCTTTC	54778
rs532823969	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59032240	CACTGTACCTGGCCT[C/T]ATTTATTACATTTTA	54778
rs532844204	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58996121	GAGTTATGTTCTTAA[C/T]TGTGATCATATGAAA	54778
rs532868882	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59068943	AGTTGGGTCTGTGGC[A/G]CGTGCCTGTAATCCC	54778
rs532870137	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990558	GGGAAGCTGAGGCAG[A/G]AGAATGGCTTGAACC	54778
rs532911419	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59017070	GTGAATTGTATAATA[C/T]TATATATTGCAATGC	54778
rs532912424	snp	A/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59038196	GAGCATAGGATCCTC[A/T]TCTGCTTTGTGTGAG	54778
rs532922787	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59018579	CTATATATACAGAAA[A/C/G]TTATAAAGGGTAAAA	54778
rs532940251	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59032794	ACCCAGAGACTTTTA[A/G]TCTCGACAGTGCATA	54778
rs532941079	snp	C/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59008019	TGATAAAGTCAAGCT[C/T]ACTAATTTTTTTAAG	54778
rs532948650	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59040229	CAAGTGATCCTCCTG[C/T]CTCAGCCTTCTGAGT	54778
rs532956745	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59086736	ACTGGGAACTCCAAG[A/T]AAGCTGGTGTTTCTA	54778
rs532957445	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59038911	CTGTTTTCTGTAATG[C/T]TTTTTAGCAGTTATT	54778
rs532959540	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58996855	GTTTTAAAAGTCAGT[G/T]TCAAAAGACTTACAA	54778
rs532974778	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59065208	AGGGCGGGGCTTTGG[C/G]TTTAGGCTCTTCACT	54778
rs532984900	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59075081	TAATAGTAACATCAA[C/T]GACTACTCATCAAAT	54778
rs533035404	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59081402	GTAGTCACAGCTCCT[C/T]GGGAGGCTGAGACAG	54778
rs533044817	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59094075	TACCCTATCTTGCTT[A/G]GGGGCTTTATTTCTC	54778
rs533048026	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59074361	TTAGGCTGTTTTGTC[A/G]ACATGGAAAATCTGT	54778
rs533057260	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59087567	TACAATAGATAATGA[C/T]AGTTTACAATAAAGT	54778
rs533078926	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59013595	GCACTGATTTGATCA[A/G]TTGTGATCAGCTGGC	54778
rs533085902	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59044322	AGGCATGAGCCACCA[C/T]GCCTGGCCATGGAAA	54778
rs533105285	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59093230	CTTCTGTAAATCTTG[C/T]AGAAATGAGAATTTG	54778
rs533146011	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59062575	AAACAGATAAATTTT[C/T]GTTCTAACAGAGCTT	54778
rs533148820	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59055904	ATAAAAGGAAATCTC[C/T]TAATATGCTAGAAAC	54778
rs533162996	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59019193	ATCCACCTGCCTTGG[C/T]CTCACAAAGTGCTGG	54778
rs533214955	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59061319	ACAACCCGTCCTTAT[C/T]TTGTACCTTTTTGAA	54778
rs533227694	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59050031	AGGCGTGAGCCACCA[C/T]GCCCGGCCCACAGTA	54778
rs533242374	snp	A/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59049423	TTCACAGGTTATAGG[A/T]TCCAGCAGTTCAGGC	54778
rs533243574	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59086270	GATTACAGGCACGTG[C/T]CACCATGCCTGGCTA	54778
rs533268191	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59073585	TCACATCTTCAGGTT[C/T]CAACTTCTTATTCTA	54778
rs533284967	in-del	-/T	0.425894	0.177655	intron-variant	RNF111	GRCh38.p7	15:59012743	CCAACTCTTTTTTTC[-/T]TTTTTTTTTTTTTGA	54778
rs533311656	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59064976	TTTATTATTTAAGCT[C/G]TTTTGGTTGGATTTT	54778
rs533347389	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59034939	ATTGTCACGCTGCTA[A/G]TAAAGACATACCCAA	54778
rs533378025	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58994433	TATTCAGATTCACCA[A/G]TTTTTAATGTTGTCA	54778
rs533391314	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59025278	GTTTATCAAGGGTCC[C/G]ACTCTTCTTTTCATA	54778
rs533447317	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59078869	CTCTCAAAAGAAGAA[A/G]AAAAAAAAAAAAAGA	54778
rs533476744	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59024879	TTTATTTTCTGTCTA[C/T]GAATTTGACTACTCT	54778
rs533483336	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59042418	GGCGTGAGCCACTAT[A/G]GCTGTCCAACATTTT	54778
rs533508504	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59078293	TCTCTGCTTTTGAAA[A/G]GTTTGTGGTCTTGAT	54778
rs533535542	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:58999546	TCACTATGTTTCCCA[A/G]GCTGGTCTCGAACTC	54778
rs533555103	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59041526	AGATTGTGCCACTGC[A/G]CTCCAGCCTGGGTGA	54778
rs533571645	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59058893	TTATCAAGACAGTGA[A/G]AGACAGCCTACAGAA	54778
rs533572248	snp	G/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59037441	TCTAGGATCTATTCA[G/T]AGAACCTTACTGGAA	54778
rs533581746	in-del	-/T			utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096153	ATATAGAATATAAAG[-/T]TAAGTTAACATACTA	54778
rs533584645	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59059175	CCAACCCAACAGAAA[C/G]ACAACCCAATTTTAA	54778
rs533603375	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59080076	TATTTTAAAAATTTA[A/G]TGGTAATGTGGGGGT	54778
rs533633642	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59017536	AGGTTTGGCTTCTAT[C/G]ACTTTAAAAGAGAGA	54778
rs533637259	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59084512	AATAATAATTGTATA[C/T]ATTTGGAGGTACAGC	54778
rs533658657	snp	A/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59074865	GTTTTGGTTTAAAAT[A/G]AGAGATGTGCAAATC	54778
rs533662108	snp	A/C			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986773	ACCCGCCTAGGCCTC[A/C]CAAAGTGCTGGGATT	54778
rs533700681	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59010503	GCCTCCTAGGTTTAA[A/G]CGATTCTCCTGCCTC	54778
rs533706193	snp	C/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59036266	TTTCACCATGGTGGC[C/T]GGGCTGGTCTCAAAC	54778
rs533715591	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59047057	TGAACTCCTAGGCTC[A/G]AGCAATCCACTTACC	54778
rs533722939	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59000091	ACAGATCCAGACCAT[A/G]TCAATAAGTATCAGT	54778
rs533762394	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58992562	GTGGCTCATGCCTGT[A/C]ATCATAGCACCTTGG	54778
rs533763965	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59070686	AGAAAGGAGCTCCTC[C/T]TTTTCTCTTTCCCAA	54778
rs533777037	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59053540	TTGCCATTTTAGCAT[C/T]GAAGTGCTACTTCTA	54778
rs533825416	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59046924	CCAGGCTGGAGTACA[A/G]TGGCACAGTCTCGGC	54778
rs533839378	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59005591	CAGTGTTTTGGTCTA[A/G]TCTTCAAGAGGAATT	54778
rs533849330	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59041022	CCAAAATATGACCCC[C/T]TTCTCTTACTCAAAA	54778
rs533859290	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59022761	GATAATAGGAAACTT[A/C]TCATTATTAATATCA	54778
rs533861772	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59065012	TATTTGTAAACAAGC[A/C]GAAGATTCCTAATTG	54778
rs533938029	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59084000	TTTATAATTTATTAT[A/C]AAATTTATTTTATGA	54778
rs533947102	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58997615	CGAGGTCAAGAGATC[A/G]AGACCATCCTGGGCA	54778
rs533991196	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58991640	AAAAAATCAGCCATA[C/G]TGACGATTTGGAGGA	54778
rs534088986	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59033794	GTTTTTTTTCATTGC[C/T]TTTCTTGGCAGAATT	54778
rs534092151	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59065410	TAACTGGGCATGTGG[C/T]GGAGAGCATAATCAG	54778
rs534105999	snp	A/G	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59058773	AGCTCAAATAAGAGA[A/G]CTTGGGGAGAAGCAA	54778
rs534117403	in-del	-/A	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:58990494	CTCTACTGAAAATAC[-/A]AAAAAATTAGCCGAG	54778
rs534118028	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RNF111	GRCh38.p7	15:59097531	CTCTGGTGACTTTAT[C/T]TTAGCTGCTAGCACA	54778
rs534119219	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59088924	TCTATGCTTGGGTGC[C/T]ATTTTAAACAACACA	54778
rs534119603	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59039929	ACCGTGTTGGCCAGC[A/G]TGGTCTCGATCTCCT	54778
rs534153379	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59086077	CTTCAGTTATTTTGC[C/T]GTAAGTGGTAATAGA	54778
rs534176988	snp	A/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59065917	TTAGGAGGCTGAGGC[A/T]GGAGAATCTGTTGAG	54778
rs534205684	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	RNF111	GRCh38.p7	15:58986591	TTGATCATGGCTCAC[G/T]GCAACCTCGGCCACC	54778
rs534215125	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59041380	CCAACATGGTGAAAC[A/T]CTGTCTCTACCAAAA	54778
rs534222109	snp	C/T			utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59095984	TGTTTTATTTCTCTC[C/T]AAACTTGAAAACAGT	54778
rs534223969	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59064561	AAAAAAAAGGAAATA[A/G]TTTGTCGACTTTGTT	54778
rs534226936	snp	A/C	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59009398	AGAACCCACTTTATT[A/C]CATTGTGCTTTTTAC	54778
rs534280073	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096644	TGTGTGCAGATGGAC[A/G]ATGGATTTAAAGAGC	54778
rs534289568	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59070169	CATGTACCACTGTGC[C/T]TAGTAGTTTAATTAG	54778
rs534298827	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59045145	TGTAAAAGGTGTTCG[A/G]TAATGTTAGCTTATT	54778
rs534299888	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59032809	GTCTCGACAGTGCAT[A/G]TGATACATCAATTAA	54778
rs534331220	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58991298	CCATCTTGAAAAAAA[A/C/G]CAAAACAACAAAAAA	54778
rs534334964	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59057506	TTTTCAGATTTAATT[G/T]TCGTGACTATGCTTT	54778
rs534342643	snp	C/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59014986	TGTCCTGGCCTCAGG[C/T]CATCTGCCTGCCTTG	54778
rs534382571	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58997739	GAGGATGGCTTGAAC[A/C]CGGGAGGCAGAGGTT	54778
rs534449809	snp	A/C	0.00597247	0.0543191	intron-variant	RNF111	GRCh38.p7	15:59036676	AAAGCCAAACCATAT[A/C]GGTGCATCAATATTT	54778
rs534467789	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59045807	TCCTTTTGTACTTCT[A/G]CCTTAAGCTGCATTG	54778
rs534483187	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59082413	TTTGAATGTTACTAA[C/T]GAGAGGGAAGGAAAG	54778
rs534502225	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59077594	TTTGCATATTAGCAC[A/G]TAAAAATCTAGCTCA	54778
rs534514218	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59024002	GTTTACCAATAATAT[A/G]TAGGAAAAAATCTTT	54778
rs534553600	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59026311	TTTTTTTTAGCTATC[A/G]TATTTTCTTAGTGCA	54778
rs534553655	snp	A/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59003905	GTGATAGCTAATGTA[A/T]TGTCAGTGATACTGT	54778
rs534558114	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59088702	TTAGCAAATATGGGA[A/C]CCTTGCAAACCTCTG	54778
rs534558583	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990384	GAAGCTGTGGGCCAG[G/T]CGTGGTGGCTCACCC	54778
rs534596029	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59075389	AAGCTTTGAGTGGCA[A/G]AGGTAATTCATGATT	54778
rs534605627	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59068583	TGCACTCCAGCCTGG[A/G]CAACAGAGCAAGACT	54778
rs534608976	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59074518	AGTTTCATGAACTAA[A/C]CTCTGCTATCTTCAG	54778
rs534657075	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59057330	TTCCCCCTTTTTTAT[A/G]TACAAGCAATTTGCA	54778
rs534665121	snp	A/G	8.23689e-05	0.00641698	missense	RNF111	GRCh38.p7	15:59081031	CCTCCGCCTCAAGTG[A/G]ATTATGTTATTCCTC	54778
rs534686820	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58995711	CCTCGTGATCCACCT[G/T]CCTCAGCCTCCCAAA	54778
rs534754769	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59050712	ACAATCAGTGCCATG[G/T]ACTTAAATCCATCAC	54778
rs534759601	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59026880	GAAGAGTTAACTGGT[G/T]TACAAACACACACCA	54778
rs534776293	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59001450	AAAAAATTCTTTTTA[C/G]TATCAGTTTAGTGGG	54778
rs534849454	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59069159	GAATTGAGTAGAAAA[G/T]ATAATTAAAGAGATT	54778
rs534853696	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59032965	GCAGACAGTCCTGAA[A/G]TGTATGTTCCATGTA	54778
rs534884760	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59024023	AAAAATCTTTTGGCT[C/T]CCTGCTGTTCTTTTC	54778
rs534939818	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59061577	CTCCTGCAACTTCCA[A/G]TGCCTCCATATAAAC	54778
rs535003442	in-del	-/A	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59002691	AGTAAAGATAAAATG[-/A]AATAAAAATGTGGCA	54778
rs535019596	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59018917	TATAACTGTATATTT[G/T]TTTCTTTTCTTTTTT	54778
rs535020555	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59002093	TAAAGCTTGTGAGCT[C/G]TTTATTTCTAGAGTT	54778
rs535059113	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59025031	GAATACTATTTCATT[G/T]TACGTGTATATCACA	54778
rs535065993	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59044093	TGGAGTGCAGTGGCG[C/T]AATCTCGGCTCACTG	54778
rs535068678	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59037785	AGGTTGCTGTGAGCC[A/G]AGATCACGCCATTGC	54778
rs535084223	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59008074	GTGAAATCTTTGCCC[A/G]TGATATAATCACATA	54778
rs535102278	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59087067	TTAGGTGAGTTAGGT[C/G]TTGGATGTACTGAAT	54778
rs535105599	in-del	-/G			intron-variant	RNF111	GRCh38.p7	15:58991579	TTGAGTGGTTAGGGA[-/G]GGCCTTTTTAGAGGT	54778
rs535150907	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59037092	TGTGCCTGCCTCGGC[C/T]TCCCAAAGTGCTGGA	54778
rs535154710	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59030501	GATTTGACCAAATAT[A/G]TTTTGTTGCTGAAGG	54778
rs535166974	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59094184	CACAATATTAAGTGT[A/G]TATAACAATTATTCC	54778
rs535185351	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59018229	CTAGATTTGTAGACT[A/G]ACATCAGTAACTAAA	54778
rs535192472	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59073351	AGGTGCGTGGTGGCA[G/T]GCACCTGTAATCCCA	54778
rs535246627	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59019356	CATTTGAAAAAATAC[A/G]GTGTTTTTAAAGGCC	54778
rs535264377	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59056905	AGGTGATAGAGTAGC[C/T]TTTTCCACATTACAG	54778
rs535339732	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59042185	GATGGAGTGCAGCAT[A/G]TTGCTGCCTCGGCTC	54778
rs535348460	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59048463	GTATAGGGGATGATG[A/G]CTGACTGAAATAGGA	54778
rs535362566	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59012261	TGACCTCAGGTGGTC[C/T]ACTTGCCTAGGCCTC	54778
rs535425429	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59017237	TGCTGTGTAGGCCAC[A/G]ATAATTTTTATTTTT	54778
rs535428768	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59091740	CCTTTTTGACACCAG[A/G]GACCAGTTTTCATGG	54778
rs535439756	snp	A/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59005883	ATATTTTCATTTTTC[A/G]GATGAGGAAATTCAG	54778
rs535471239	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59084660	GTTTTGAAATAAACG[C/G]TACGTTATTCTTCAC	54778
rs535488008	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59017834	ACAATCTCGGCTCTC[C/T]GCAACCTCCACTTCC	54778
rs535493244	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58994638	GCCCGCCACCACGTC[C/T]AGCTAATTTTTGTAT	54778
rs535502170	snp	A/G	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:58991516	TAAGTGCCATGAGGA[A/G]AATAGGACCATGTGA	54778
rs535527888	snp	C/T			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020477	TTGTGAGGTTAGATA[C/T]ACCCTTCATTTTGCT	54778
rs535539980	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59072907	AACAAAACACTTCCA[A/G]CTGGGCATGCTGGCT	54778
rs535579457	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58987911	TTTTGGTGGCGGTGA[C/G]AGACACTGTTCTTGA	54778
rs535584443	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58994220	TTTTTTATATTTTTG[C/G]TAGAGATGGGGTTTC	54778
rs535585393	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59065882	CAGGCGTGGTGGTGT[G/T]TGCCTATGGTCCCAG	54778
rs535593888	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59023619	CTCATTTGTCAGTGT[C/T]ATCTGCCAATAATGA	54778
rs535610926	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59079085	AAAGGGTTTTTGGGA[A/G]TGTGGAATATGTCAC	54778
rs535620205	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59014238	GTGTTTCTTTACTTT[C/G]TGGCACTACCAGATG	54778
rs535622587	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59042536	CTAGCAAAATTAGCC[A/C]ATTTCCCCCCAGTCC	54778
rs535644249	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59072125	TCTGAGACTTCAGCA[A/G]ATTGTAAACTTTTTG	54778
rs535676829	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	RNF111	GRCh38.p7	15:58987436	GATGTAGTCAAGATT[A/T]GGCTTAAATGTTGAA	54778
rs535729530	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59085125	CTTGAACCACAATGA[C/G]TTTTGAGGCAGAACA	54778
rs535771686	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59054485	GTCTCATCATAGACT[C/G]TTGATTTTTCAAGAA	54778
rs535811927	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58998982	TTTTTCACTGATAGT[A/G]TGAGGTTTCATTGAT	54778
rs535838146	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59060345	TGGTGAGACTCACAC[C/T]TGTAATCCCAGCTCT	54778
rs535884699	snp	C/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59060220	AGGCAGAAATGAAAT[C/G]GGCTTTTATTTCATT	54778
rs535895715	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59072499	CGCTCTGTTGCCCAG[C/G]CTGGAGTGCAGTGGC	54778
rs535901142	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59036847	TTGGTTTTATTTGCT[C/T]TTTGAGACAGTCTTA	54778
rs535915790	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59046991	TACCACCTCAGCCTC[C/T]GGAGTAGCTTTTGTT	54778
rs535922688	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59083229	TAGGAAGAGAAAATA[C/T]AGTAAACTGGGATGC	54778
rs535928233	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59053484	AGTATATATTCATAT[C/T]TCTGACATCTGTTAC	54778
rs535948150	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59090060	AATGTGGTGGGGAAC[A/G]GAATGTTTTTGACTC	54778
rs536074870	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59065191	GGGTTAAGGATGGCA[G/T]CAGGGCGGGGCTTTG	54778
rs536096760	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59035605	GCAAATTTTGCAAAT[G/T]TTTATGCTCTGCTTC	54778
rs536133561	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59035115	CTCCCATTTATAAAA[C/G]CATCAGACCTTGTGA	54778
rs536136063	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59064399	AAATTAGCCGGGCTT[A/G]GTGGCGGGCGCCTGT	54778
rs536138628	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59071488	AAGAGTTCGAGACCA[C/G]CCTGTGCAACATGGT	54778
rs536244298	in-del	-/AA	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59049323	TAGCGTAATGCCCTC[-/AA]GTTTTATTTTGTTTT	54778
rs536286905	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59079906	TTTGGAAAAATGTTT[A/T]CACCCTATTATGACA	54778
rs536305246	snp	C/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59024298	TTCCTTTTACTCATT[C/T]TTTTACAGATTAATG	54778
rs536310441	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59003926	GTGATACTGTATCTT[A/C]TAAAATATTAATAAG	54778
rs536317590	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59010759	TTCTCCCTGCTTGAA[A/G]GTAATGGAAAAGTTG	54778
rs536327292	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59033114	GGAATAGGGTAATGG[A/G]CCTAGGGAGAGCTTT	54778
rs536356047	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59009973	ACAAACAAACAAAAA[C/T]TAAAATGATTTTGCT	54778
rs536358635	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59034932	TTAATCCATTGTCAC[A/G]CTGCTAATAAAGACA	54778
rs536402914	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	RNF111	GRCh38.p7	15:59097419	GATCGTTTGAAACGT[G/T]TTTCTTACTCTGGTG	54778
rs536432068	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59039124	CACGTGCCACCATAC[C/T]TGGCTAATTTTTTAT	54778
rs536498508	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59044198	ACCATGCCCAGCTCA[C/T]TTTTGTATTATTAAT	54778
rs536546556	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59008320	CCTCCTGAGCTCAAG[C/T]GATCCTCCTGCCTCA	54778
rs536568159	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59051002	GGATTCTATTTATAT[A/G]ATCTTATCTAATGTC	54778
rs536602671	snp	C/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59027433	AGATTTTATTTCACT[C/G]GGTTTTTAGTATATT	54778
rs536628208	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59011190	TCTGTTCTTCGAATT[C/T]CACTGTCTTATCCTT	54778
rs536628228	in-del	-/AGAC	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59019058	CCACCCGTGTAGGTG[-/AGAC]TTCAGGCACGTGCCA	54778
rs536656885	in-del	-/CCT			intron-variant	RNF111	GRCh38.p7	15:59009047	TCACTGCAACCTCCA[-/CCT]CCTGGGTTCAAGCGA	54778
rs536662935	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59036180	TCCTGGGTTAAAGTG[C/T]CTGAGTAGCTGGGAT	54778
rs536668172	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58991221	AGAATTGCTTGAACC[C/T]GGGAGGTGGAGGTTC	54778
rs536684808	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59056750	TTGGTTTTTGTTTTG[A/C]AGCACTGTAAATGAT	54778
rs536706782	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990752	CTTTAATAGCTTTCA[C/G]ATGGTACTAAAAATG	54778
rs536706881	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58997670	AAAAATACAAAATTA[G/T]CAGGGCGTGGTGGCA	54778
rs536797022	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59088575	TTAAAAAGTAATGTC[A/G]GAGATTTATTTATAA	54778
rs536799037	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59081855	AACATAAGGAGACCT[C/T]GTCTCCACCAAAAAA	54778
rs536808150	in-del	-/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59075861	TAATTTAAAGATTAT[-/G]TTTTTTTGGTTATAT	54778
rs536838951	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59002572	AAAAAAAAAAAAGAG[A/G]GAGAGTGACCAAACT	54778
rs536872488	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59055328	GGATATTATTAAATG[C/T]GTAGGGTGTTATTTT	54778
rs536872591	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990136	TTTGCTTGCTATACA[C/T]TAGATCTCCGAGTTT	54778
rs536891732	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59031965	TTTTTCTGAAACAGA[A/G]TCTCACTTTGTCACC	54778
rs536897048	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59045098	AGCTTTGTATCATTT[A/T]TCATTGAGGTTTCAA	54778
rs536907126	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58995552	CAACCTCTGCCTCCC[A/G]GGTTCAAGCAATTCT	54778
rs536914730	in-del	-/TTA	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59030259	TTCTCATTAGAGAAT[-/TTA]TAATAGAGTAGTATG	54778
rs536923678	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59008729	CTCTTTTCCTGCCTC[A/C]TTTTGGATTGAGGGT	54778
rs536930998	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59073947	ACATTAATCTACTTA[C/T]ACATCATCAGAGCTC	54778
rs536964828	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59057227	ACATCTCCTCCCCAG[C/T]GAACAAAAAATTGTC	54778
rs536982767	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	RNF111	GRCh38.p7	15:59095430	CTATATGGAGTTCTG[A/T]GTTAAATACCATCCT	54778
rs536991951	snp	C/G	0.00517822	0.0506191	intron-variant	RNF111	GRCh38.p7	15:59080305	TTTGTATTTTTAGTG[C/G]AGACGGGGCTTCGCC	54778
rs537032426	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59000915	AAAACGAAATCTGCT[C/G]TGGTGGGGAAACAAA	54778
rs537064933	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59085954	GTATTAAAATCTGCA[C/T]GTATAATTTGCATCA	54778
rs537107275	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59049587	CTCAGCTGTAGTGCT[C/T]TATATGCTCATTATA	54778
rs537156659	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59068467	AAAAATTAGCTGGGT[A/G]TGATGGTGTGTGCCT	54778
rs537179826	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59092939	CAGGAGTTTGAGACT[A/G]CAGTGAGCTTTGAGC	54778
rs537185050	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990351	CCTCATGAAATGTGT[A/G]TGTGTAAAACCTGTC	54778
rs537191333	snp	G/T			upstream-variant-2KB	RNF111	GRCh38.p7	15:58987309	TTAGCGCATATGATA[G/T]GGGTATCATTTGTTG	54778
rs537206167	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59032378	TATGATGGATTCAGC[A/C]ATAGTAAGAACAGTT	54778
rs537211758	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59067983	TTATTGAGTTCGCAA[A/C]ATGTCAACTAGTATT	54778
rs537220473	snp	G/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59074439	ATAACTTACTGTAGC[G/T]TCTACATCAGCACTT	54778
rs537227435	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59002481	CGGTTGAGTAACATA[C/T]GTAATAATCTTATGT	54778
rs537276032	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59035351	CCCCCAAAGTCTTAA[C/T]TCATTTCAGTATTTA	54778
rs537284234	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59061117	GTAGCATTATTCTTA[C/T]GTACATTTTATGTGA	54778
rs537311591	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59037739	TACTTGGGAGGCTGA[A/G]GCAGGAGAATGGCTT	54778
rs537360291	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59066541	CTTGAACCCAGGAGG[C/T]GGAGGTTTGGTGAGC	54778
rs537400211	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59030354	TGTAGTAACCATCTA[A/G]ATGTACAGAAACATT	54778
rs537425051	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59043213	AGGCTGGAGTGCAGT[A/G]GTGCGATCTCCGCTC	54778
rs537439257	snp	G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59007494	TTATTTTTTCTCTAA[G/T]TTTTGGCTATTATGA	54778
rs537448936	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59036345	GGATTACAGGTTTGA[C/G]CCACCGCACCCGGCC	54778
rs537469720	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59093432	CTCACTGCAACCTCC[A/G]CCTCCTGGGCTGAAG	54778
rs537500249	snp	A/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59050121	CCAGGCTGGAGTGCA[A/T]TGGCGTGATCTCGGC	54778
rs537510742	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59056020	TGTAAATTTACATAA[A/C]ATTCTTTGTGGTTAT	54778
rs537515350	snp	A/G	0	0	intron-variant	RNF111	GRCh38.p7	15:59042052	TTATATATTAGCAAT[A/G]TAAGTCCTATATAAT	54778
rs537528628	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59079022	GAACGTCTAGGAAAC[A/G]ATATCAAGAACTTTT	54778
rs537630284	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59005647	TAGTTTGAGGTGGGT[A/G]TAGCTAGAGGATTGA	54778
rs537631721	snp	C/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59041592	TACTGCAATAAATAG[C/T]TTTTTGTATATGTCA	54778
rs537646935	in-del	-/A	0.00119737	0.0244387	utr-variant-3-prime	RNF111	GRCh38.p7	15:59095393	TTCCTTAATTAGGAC[-/A]AAAATGGCTGCTGTA	54778
rs537655830	in-del	-/A	0.433527	0.169758	intron-variant	RNF111	GRCh38.p7	15:59026723	AGGGATGGATTTTAG[-/A]AAAAAAAAATTTAGA	54778
rs537674383	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59018311	CATTTCTGAGTTTCT[A/G]CCCTATTCTGTCATT	54778
rs537680130	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:58996419	TCAACTGAAAAATGC[-/A]AAAAAAAAAAAAGTA	54778
rs537710658	snp	G/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59076528	CAAGCTTTGGGAGTT[G/T]TAAAAGGATTTTTAT	54778
rs537724690	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59011769	CTCTTTAAATGTCTT[A/C]TCTCTAAATACAGAC	54778
rs537727692	in-del	-/CAA			intron-variant	RNF111	GRCh38.p7	15:59069073	AACAAGACTCCGTCT[-/CAA]AAAAAAAAAAAAAAA	54778
rs537755332	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59017723	TCCTGGAGGTTTGTC[C/T]TCCAGGTTTGTTACA	54778
rs537760672	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59024319	CAGATTAATGCAATT[A/T]AAAAAAATACTAATT	54778
rs537844214	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59017073	AATTGTATAATATTA[C/T]ATATTGCAATGCAAT	54778
rs537861750	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58994156	GATTTTCCTGACTCA[C/T]CCTCCCAGGTAGCTG	54778
rs537896910	snp	C/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59088024	TTTATAAGCTTGGCT[C/G]TGAAGGGAAAGTGAA	54778
rs537900561	snp	A/C	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:58993135	AGATTGCGCCACTGC[A/C]CTTCAGTCTGGGTGA	54778
rs537900610	snp	A/G			utr-variant-3-prime	RNF111	GRCh38.p7	15:59095328	CAATCATGTACTTTA[A/G]TTTAATGTATAAAGA	54778
rs537927525	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59035813	CTCTGCCTGGACTTT[A/G]TTGTCCATATCACTG	54778
rs537946271	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF111	GRCh38.p7	15:58987360	TGTTTTTGTTTACGT[A/G]TATCTGTAAATGTAT	54778
rs537975111	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59028825	TGCTCTGTTGCTCAA[A/G]CTGGACTGTAGCGGT	54778
rs537980222	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59085010	ACAAGGGAAATTTAG[C/T]CTGCCTTCTCCTAGA	54778
rs537987228	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58992288	GATCTCAGGTGATTC[A/G]CCCGTCTCGGCCTCC	54778
rs537990747	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59006273	GATGAATTTTGGCAA[A/G]TGTGTCTGTCCATGC	54778
rs537991183	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59078433	GTAGTTCCTGCTCTT[C/T]AGGAGGCTGAGGCAT	54778
rs537992705	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59084539	CAGCATAGTATTTCA[A/G]TACATACATACATTG	54778
rs538010179	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:58991939	AGTTATTGTAACTTT[C/G]TTAGGGATGATAATG	54778
rs538010579	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59019330	GGATCCTTAGGTGTA[C/T]ATATTCAGGCCATTT	54778
rs538012113	snp	G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59035090	GCAAGAGAGAGATTG[G/T]GCAGGGGAACTCCCA	54778
rs538043914	in-del	-/AG	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59064795	GAGCTACTGTGTAAC[-/AG]AGGTTAGAGCACAGA	54778
rs538055324	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59090763	TTTGCCTTACTGTCT[A/G]TGAGAAACATTAAGT	54778
rs538068200	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58998936	ATGTCTGGGTGAAAG[A/G]TCTATGTAAAGTGCA	54778
rs538154796	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59011039	AATTTGGCATCTTGA[A/G]GATGAAAAATTGTCT	54778
rs538162846	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59053650	TGAAAACCAGTGTTA[A/T]GTACCACACCTATCC	54778
rs538228836	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59003477	GATCCCTGCTTACTG[C/T]AACCTCCACCTCCTA	54778
rs538239098	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59009827	TGGGCATGATGGCTC[A/G]TGTCTCTAGTCCCAG	54778
rs538261519	snp	A/G	0.00358779	0.0422022	utr-variant-3-prime	RNF111	GRCh38.p7	15:59097324	TAAACTGATAATTTG[A/G]AACATTTTTCTTACT	54778
rs538296567	snp	A/C	0.00478085	0.0486577	intron-variant	RNF111	GRCh38.p7	15:59052797	TGCCCAGACTCTTTC[A/C]CATACTTGAACTAGA	54778
rs538315819	in-del	-/TTC	0.00478085	0.0486577	intron-variant	RNF111	GRCh38.p7	15:59052794	TGTTGCCCAGACTCT[-/TTC]CCATACTTGAACTAG	54778
rs538340489	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59065102	TTACTCTTGGGTACT[A/G]TAAAATCAAGGCTAG	54778
rs538416118	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59070907	TTGCACAGTTGCTGT[A/G]TATAATTCCATATAT	54778
rs538424302	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59053104	GAAACTTGTGCTGTT[A/G]CTGTGTTAGGGCACC	54778
rs538444882	snp	A/C	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59040790	CTTTTTGCCCTTGGC[A/C]AGTTTTCTGTGTGGT	54778
rs538453839	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58991679	ACAGATAGCAGGGGC[A/G]GCAAATGCATTAGGT	54778
rs538476504	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59034354	TGAAAATGTTGTTGG[C/T]TGTTGTTACCAGAAT	54778
rs538485092	snp	G/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59039234	CTCCCAAAGTGCTGG[G/T]ATTACAGGTGTGAGC	54778
rs538507059	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59040016	CACTGCGCCCTGCCC[A/G]ATTTTCTTTTATTGG	54778
rs538514912	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59076782	AAATACTCTAAGGCT[A/G]TGTAACATATTTACT	54778
rs538516150	in-del	-/CTC	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59062706	GATTTTATTACTCTT[-/CTC]CTCATTCTACAGGTG	54778
rs538534780	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59069966	GCTTTGATATGATAT[A/G]GCTTTCATCCCTACC	54778
rs538550676	snp	A/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:58991161	AATTAGCTGGGCATG[A/G]TGGTGGCATGCGCCT	54778
rs538555863	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59069249	CCTATCTCTTGGGAA[C/T]GAGGGAGCATCAAGA	54778
rs538570857	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59090848	GGATCACTTGAGGCC[A/G]GGAGTTTGAGACCAG	54778
rs538578955	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59033667	GGGGAATGAGAATAT[A/T]GTAATTGAATGTCAT	54778
rs538600357	in-del	-/G			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:58988080	TAAGGTGAGGGGAAC[-/G]GGGGGGGAGGGGATC	54778
rs538618623	snp	C/T	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:59046401	TTTCACCATGTTACC[C/T]AGGCTGGTCTCGCAC	54778
rs538681758	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59052178	ATTTTTTTAAAAAAC[A/C]TTTTTGACAGATAAG	54778
rs538713233	snp	A/C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59044776	GATTTTCTTTTAAGT[A/C/T]GTGCTATTTAATAAG	54778
rs538739095	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59015846	TTATAGCATGTTTAT[A/G]ACGTATTCTGGTTAT	54778
rs538771124	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59029297	TGTGACTTCTGTGTT[C/T]TTGCCTTTAATTAAA	54778
rs538802758	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59008635	TCTGTCCTTACACCA[A/G]TAGCCCCAGTGTTGA	54778
rs538805502	snp	G/T	3.295e-05	0.00405881	missense	RNF111	GRCh38.p7	15:59081174	TCCTCCTACACACCA[G/T]CCAATTTCGCACCAT	54778
rs538807626	snp	A/C	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59087263	AAACCTTAGAGAATG[A/C]CAATACTGTATTTAA	54778
rs538826576	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59044125	AACCCCCACCTCCCG[A/G]GTTCAAGCGATTCTC	54778
rs538828685	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59051368	GAGGCTGAGGCAGGA[A/G]AACAGTGTGAACCCA	54778
rs538835555	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021496	TATTTTTAGGTGTAA[A/G]AGAAAGTCTTAAATG	54778
rs538869708	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020998	AGTGGTGATTTCTGA[G/T]ATTTTGGTGCACCCA	54778
rs538889673	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59050856	TAGACCCTATGTTGT[A/G]CAGTAAATTTCCAGT	54778
rs538900458	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59050272	CTTGATGTCTACAAC[A/T]TCGCTTTTTCTTGTA	54778
rs538954969	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990709	ATTATTGCTATTGTT[A/G]TCCCATTGTAGATAT	54778
rs538955675	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59026910	ACAGCATACACCAAA[C/T]CACCCCCCCTTGCTC	54778
rs538975506	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59013887	TCTGCCTCCCAGGTT[C/T]AAGTAATTCTTATGC	54778
rs538983211	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59033071	GCTGTCTGAACTGAG[A/G]GAAAAGATTAATTTC	54778
rs538997561	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59075561	TGATAGTATGTTTTC[G/T]CAAGGAGTCCTAAAG	54778
rs539044091	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59026212	ATAGTCTTAATGGGT[C/T]TTTCCTCCTTTTGCT	54778
rs539044405	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58997130	TACAAAGTGTACCAA[A/G]TTTATAAGGTACAAA	54778
rs539048777	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59032245	TACCTGGCCTCATTT[A/G]TTACATTTTATACAT	54778
rs539056473	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	RNF111	GRCh38.p7	15:58987626	GAGGCGTGAAGGCTA[C/T]TGCGCTCTCACTTTC	54778
rs539080649	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59025808	CGATCTCGGCTCACC[A/G]CAACCGCTGCCTTGC	54778
rs539093347	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59002484	TTGAGTAACATATGT[A/C]ATAATCTTATGTAAA	54778
rs539114623	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59054138	GAGACGGGGTTTCAG[C/T]ATATTAGCCAGGCTG	54778
rs539115108	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990412	CCCCTGTAATCCCAG[A/C/T]ACTTTGGGAGGCCAA	54778
rs539170626	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59025136	ACGATCCGCCCTCCT[A/C]CGCCTCCCAAAGTGC	54778
rs539182632	snp	G/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59002019	GATGACGGAAAATGA[G/T]GATAAAATGGCGAAA	54778
rs539219267	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59008259	GTCTTTCTCTGTTGC[C/T]CAGGCTGCAGTGCAG	54778
rs539237257	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58994681	CGAGGTTTCACCCTC[G/T]TGGCCAGGCTGGTCT	54778
rs539240053	in-del	-/TAAAGC	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59051910	ACCTTGGAAAAAACA[-/TAAAGC]TATTGTAATTACTTT	54778
rs539248069	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59094312	TTTAGTGAGGAAAGT[A/G]TAGTTACTATATATT	54778
rs539260541	snp	A/C	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:59070734	CCCTTTCCTTTCAGC[A/C]CCCAGAGTTCCTTTT	54778
rs539275608	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59018843	TTTTAAATAAGAAAA[G/T]GATGAAAAAAAGTTT	54778
rs539276430	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59056676	CATAACTTTCAGAGT[A/G]TCAGTACCCAGTTGT	54778
rs539292142	snp	A/T	0.00597247	0.0543191	intron-variant	RNF111	GRCh38.p7	15:59014230	TCTTTTGTGTGTTTC[A/T]TTACTTTCTGGCACT	54778
rs539332968	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59062312	CTTTCCAAAGTGTTG[A/G]GATTACAAGTGTGAG	54778
rs539366213	snp	C/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59057388	TCAAAGTGTCCCATA[C/T]AGATTCACAGGTACT	54778
rs539369460	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59048484	TGAAATAGGACTTGC[A/G/T]AGCTCTTTTGGGGTT	54778
rs539393662	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59000445	GACCGGGCCTGGTGG[C/G]TCACATCTGTAATTG	54778
rs539467364	snp	A/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59068405	TGAGGTCAGAAGTTC[A/T]AGACCAGCCTGGCCA	54778
rs539475734	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990063	CCGTTCTATGGGTAA[C/T]GTTATCTTATGAAAT	54778
rs539496997	snp	C/G	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021950	ACTGCAACCTTGCCT[C/G]CCAGGTTCAAGCGAT	54778
rs539530517	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59067914	GAGGTTTTCAGTTTA[C/T]GGAGAATCAAAATGT	54778
rs539558894	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59018204	AAAGATGGGTTCAAA[A/G]ACAACATGCCTAGAT	54778
rs539562355	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58995480	GTTTTTTTTTTTTGA[C/T]GGAGTCTCACTCTTG	54778
rs539562917	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59060288	GTATCTTATATGTTA[C/T]TGTATATATTTTAAT	54778
rs539582336	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59080208	TCACTGCATCCTCCA[C/G]CTCCCAGGTTCAAGC	54778
rs539608098	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59073507	AAAATAAATAAACTA[A/C]TTTCTTTGCTCCTCC	54778
rs539669825	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59066514	ACTCAGGAGGCTGAG[A/G]GAGGAAAATCGCTTG	54778
rs539701947	snp	A/G	0.00119737	0.0244387	utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58987963	ACGTCTGAGGCGCAG[A/G]TCGCTGGCTCTCGAC	54778
rs539734450	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59072748	TGAGCCACCACACCC[A/G]GCCTGTCATTTCCAT	54778
rs539746936	snp	A/G	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59072259	GAAGTTTGCTGCATT[A/G]ATTGACTGTTACTTT	54778
rs539800114	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59042231	TCCCACGCTTAAGCA[A/G]TCCTCCCACCTCAGC	54778
rs539825243	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF111	GRCh38.p7	15:58987001	AGGTAAATACGTTAT[C/T]CCAATTTATAGAGGA	54778
rs539838534	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59080261	TAGTAGCTGGGATTA[C/T]AGGTGTGCATCACCA	54778
rs539885166	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59055113	ATAAACTAGCTCACG[C/G]AAGTAATATTTCTTA	54778
rs539894152	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59018585	ATACAGAAACTTATA[A/G]AGGGTAAAAGACCCC	54778
rs539897642	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59054623	GACAGTGGCTCGGTA[A/G]TTAACTTTATACTCC	54778
rs539899323	in-del	-/C			intron-variant	RNF111	GRCh38.p7	15:59082078	GGAGACCCTGTCTCT[-/C]CCCCCTCTCCCCAAA	54778
rs539903315	snp	G/T			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020621	TGACTAATATTTAAG[G/T]ATTTCAGAATACTTT	54778
rs539957585	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58998523	CTTATTTTGAGAAAA[G/T]AACTTGTTTGATTTA	54778
rs540004215	snp	A/G	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59083307	AATCCCAGCACTTTG[A/G]GAGGCCAAGGTGGGC	54778
rs540007900	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59008257	GAGTCTTTCTCTGTT[G/T]CCCAGGCTGCAGTGC	54778
rs540021700	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59017882	CCTGCTTCAGCCTCC[C/G]GAGTAGCTGGGATTA	54778
rs540030947	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59040172	TAGGCTGGAGAGCAG[G/T]GGTACACTCAATAGC	54778
rs540038338	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59024286	TGTTTTACTTCCTTC[C/G]TTTTACTCATTCTTT	54778
rs540050826	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59005052	TTTTTTTCTTGTCAA[A/G]TTCACTTTATGGGCT	54778
rs540073709	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59023712	TTCCAGAAGAATGTT[C/T]TATAACAGTGAATTC	54778
rs540075604	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59030217	AACTGAAATGCAGTA[A/G]TTGTGTCTACTATCA	54778
rs540079307	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59089545	GTTATGTATTCTTAT[C/T]GAAGTCAAATTTTAT	54778
rs540080361	snp	A/T	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:58993909	TTTAAGAAATTCTAT[A/T]TATGGCTAGGTGTCA	54778
rs540086365	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59007581	ATGGAATTACTGGAT[C/G]ATACGTTAGATGTGT	54778
rs540095422	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59045138	TAAGCCATGTAAAAG[A/C/G]TGTTCGATAATGTTA	54778
rs540142415	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59015150	CAAAGTCGAATTTTT[A/T]AAATTCTGATATTTT	54778
rs540158182	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59031857	AATTGCAGTATTAAA[C/G]CATGACTCTAATGCT	54778
rs540227986	in-del	-/AA			intron-variant	RNF111	GRCh38.p7	15:59044944	GTTCAAGTTATGCAT[-/AA]AGTCCTTTTTAGAAA	54778
rs540252228	snp	A/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59042760	GGCCTGTTTATGGAG[A/T]TTTTACTCCGTCTTA	54778
rs540261739	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59058236	TACCAAATGTTATTA[C/G]AGAGCTTGTATTTTT	54778
rs540322643	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59057566	TTAAGCAACCATTTT[A/T]AAATTAGTTCTTTGA	54778
rs540405307	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:58997944	GAGTCTCACTCCGTT[A/G]CCCAGGCTGGAGTGC	54778
rs540472710	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59026548	AGATCAGCCAATAAT[G/T]TTTACAAAAATAAAA	54778
rs540475487	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59046069	TGATAATAACATTTC[A/G]CAAATATTCCAGAAT	54778
rs540487730	snp	A/C	0.000153521	0.00875997	intron-variant	RNF111	GRCh38.p7	15:59092468	GTTTTTCAAATAAAC[A/C]CAGACTTTACTCAGT	54778
rs540509883	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59032685	CTTGGGCTCTCAATA[C/T]TTTTTCTTTAAGTAC	54778
rs540535001	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59039181	GTTGGTCATGCTGGT[C/T]TCGAACTCCTAACCT	54778
rs540537159	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58997368	AAGTTCTCATTTTCT[A/G]TGTAACTGATGTGAA	54778
rs540542003	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59009522	AAAAAGTCTTTAGAA[C/T]TTGATAATTTCAGAT	54778
rs540549373	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59068812	CTGGGCGCGGTGGCT[C/T]ATGCCTGTATTCCTA	54778
rs540609067	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58990502	GAAAATACAAAAAAT[C/T]AGCCGAGCTTAGTGG	54778
rs540627156	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59009166	GGTTTCACCAAGTTG[A/G]CCAGGCTGGTCTTAA	54778
rs540721173	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59043733	TAGAGTCATTTGCTT[A/G]TACCTTCAGTAACTT	54778
rs540722575	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59063402	CTGCCTCTCGATAAT[C/T]CTGCTAGAGTTACTG	54778
rs540742022	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59014446	GGAATAGTGAAGGGT[A/G]AAAATACCTGCAGTA	54778
rs540743415	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021214	GGAGTGCAGTGATGC[A/G]ATCTCGGCTCACTGC	54778
rs540777497	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58992310	TCGGCCTCCCAAAGT[G/T]CTGGGATTACAGACG	54778
rs540779247	snp	A/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59013957	CCACGCCTGGCTAAT[A/T]TTTGTATTTTTTAGT	54778
rs540784033	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59069513	TTTCAGCTTGAGTCA[C/G]TTGTAGGTAGGATCT	54778
rs540819731	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59052071	CTGTAATGAATACAA[C/T]AAATCCATAGAAGAG	54778
rs540854443	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59049876	CCTCCTGAGTAGCTG[A/G]GATTACAGGTGCGTG	54778
rs540856264	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59025720	AATGCCAAGTCATCT[A/G]TGGCTTTTTTTTTTT	54778
rs540859051	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59011920	TTCACTACCAAACTA[A/G]GATTGTCAAAGTTGG	54778
rs540896119	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58990510	AAAAAATTAGCCGAG[C/G]TTAGTGGTGTGCGCC	54778
rs540906197	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59075705	TGTGATAAAATCTTA[C/T]GCTTGATTTTTAAAA	54778
rs540965543	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59074974	AAGAGAGGAGAGCAG[C/G]GTAATGGGGAAACAT	54778
rs540967210	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990146	ATACATTAGATCTCC[G/T]AGTTTATTGTTAACC	54778
rs540987591	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59077700	GGTTGAGTTTATGTA[C/T]AGTTTAACTTCCTAG	54778
rs541027981	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59025259	CTACTAGGAAAGGTA[A/C]TAAGTTTATCAAGGG	54778
rs541033571	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59003391	ATTACAGGTGTGAGC[C/T]GCCACACCCGGCCTT	54778
rs541062039	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59044236	GGGTTTTGCCATGTT[G/T]GCCAGATTGGTCTCA	54778
rs541078010	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59051111	TCTTCTAAATAAGGA[G/T]GCACTTTCCAAGTTT	54778
rs541105599	snp	A/G			utr-variant-3-prime	RNF111	GRCh38.p7	15:59097220	TATATGTCAAAATGA[A/G]CATTTCAGTGGTAGC	54778
rs541113097	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:58998666	TAAATGAAGTGAGCC[A/G]TTCACTTCAAGAAAA	54778
rs541130369	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59071773	TGGTTTATTTCCCAA[C/G]TTAGTTGATGGGCTT	54778
rs541141365	snp	A/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59056824	CTCAGTTAATTAAAT[A/T]TAGGGTGACTATTTT	54778
rs541167496	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59080010	AAATAGATAATTCTG[A/C]GAACACATACAAGCG	54778
rs541253616	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59056401	AGTGGTAGAATTTAG[A/G]AATATATGAATGAAT	54778
rs541260644	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59019678	TTTAAAAGTATTTAA[A/G]CCAGGCGTGGTGGCT	54778
rs541275303	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59027703	TGGCTAATTTTTGTA[-/T]TTTTTAGTAAGACAG	54778
rs541312377	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59061846	CTTTCCTCTAATGGG[C/G]TTCTGACTCCTTTCA	54778
rs541315620	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59048930	ATCCTGTCTCTTTAA[A/C]AAACAAACAAACAAA	54778
rs541322902	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59068037	GAGTAAAAGAAGTCA[A/G]GCGTTCCATGCTACT	54778
rs541331180	snp	C/T	0.0134861	0.0810011	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096198	GAGGAAGTTTTAATC[C/T]ACTTCAGGATGCATA	54778
rs541339811	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59054903	GGCCTCACCTTTCTA[A/C]AAGATTTATTTTTTT	54778
rs541395450	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59092016	CTGGTTTGCAGCCCA[C/G]GGGTTGGAGACTCCT	54778
rs541451328	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59054158	TAGCCAGGCTGGTCT[C/T]GAACTCCTGACCTTG	54778
rs541488229	snp	A/G	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:59064363	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	54778
rs541519676	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59001081	TATCATGGATAAGGA[A/G]ACATTTGAACACAGA	54778
rs541555716	in-del	-/AA	0.4087	0.193169	intron-variant	RNF111	GRCh38.p7	15:59078553	TGAGAACCTGTCTCT[-/AA]AAAAAAAAAAAAAAA	54778
rs541590734	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59042918	TTTGGGGGTGGGGAG[A/G]TCTATGATGGTATTT	54778
rs541626380	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59072429	GATGTGATATTCTAA[A/G]TCTTTCGCTGTCATT	54778
rs541629362	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59022616	ATTGTTTCTGTGGAT[A/G]TCTGTTAAGGTTAAG	54778
rs541633907	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59092993	GGCAATAGAGTGAGA[A/C/T]CCTGTCTCTGAAAAA	54778
rs541638314	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59007115	TGAAATGCACAAATC[G/T]TAAGTATACCATTTA	54778
rs541639124	snp	G/T			utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58987862	ACCCACGCCGGCTTA[G/T]CTGGGCCGAGTCCAG	54778
rs541677310	snp	A/G/T			intron-variant	RNF111	GRCh38.p7	15:59012090	GTGGTGCGATCTTGC[A/G/T]TCACTGTAACCTCCG	54778
rs541709840	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59035341	TCCCAACAGTCCCCC[A/G]AAGTCTTAACTCATT	54778
rs541760566	snp	G/T	0	0	intron-variant	RNF111	GRCh38.p7	15:58999249	GTCATTAGAGAGATT[G/T]GCAAAAAATGTATAG	54778
rs541775556	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59045144	ATGTAAAAGGTGTTC[A/G]ATAATGTTAGCTTAT	54778
rs541783037	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59041230	AACAGTTTGCAGACT[C/T]TTTTTTATTATTTTA	54778
rs541845729	in-del	-/AAC	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:58996632	TTGTATGTGATTGAA[-/AAC]AACTCATCAGTACTT	54778
rs541847265	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59082976	AAAAACTAATATAAA[A/G]TAATTAGACTATAAA	54778
rs541849736	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59024401	GATGAGATTCCTGCT[C/T]CCTTGGAACTTATAT	54778
rs541903283	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59026951	TTGTCTCATTGGACA[A/G]ACTAAACTGATCAAA	54778
rs541969695	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59016595	ATTTTTCATCTTGCT[C/T]GGCCCACCATAATTT	54778
rs541970780	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59013542	CCCTGCCTTTCTCAT[C/T]ACATTGTATCAGGAG	54778
rs542021909	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58993263	CCTGTAATCCCAGAA[A/C]TTTGGGAGGCCAAGG	54778
rs542029990	snp	G/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58987680	TGTCGTGCTCTCCTC[G/T]GTAGGGGAGGAATTG	54778
rs542072384	snp	G/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:58999768	TAAAGAAAAGGGGTT[G/T]AATTGGCTCAAGGTT	54778
rs542086700	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59071791	AGTTGATGGGCTTTC[C/T]CTAAAATCGTATTCC	54778
rs542095995	snp	A/G	0.000399281	0.0141238	intron-variant, synonymous-codon	RNF111	GRCh38.p7	15:59022565	CCTTAATCTCCTCAC[A/G]TGGCTATCCCTTGTG	54778
rs542109850	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58992712	GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGTGA	54778
rs542120326	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF111	GRCh38.p7	15:58986868	TGAACAAAAAAAGTA[C/T]TGAAAAAGATGAGTT	54778
rs542124202	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59080552	ATTTATGCTACAGAA[A/G]TGATCTCTATATATG	54778
rs542135257	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59028079	TGATCTGCCCGCCTC[A/G]GCCTCCCAAAGTGTA	54778
rs542149530	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59064701	CAGGTTAAGAACCTT[C/T]ACAAAAGGGTTTGGG	54778
rs542163594	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59070977	GTATGGTTCCACTGA[A/C]CCTAAGCAGTAGGTT	54778
rs542185475	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59078037	GAAGACAATATGGCA[C/T]AGTAGAGCACTAGCT	54778
rs542185627	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59076838	TGAAATGAAAGCTTA[A/G]TAAACACTTGGCTGA	54778
rs542191411	snp	C/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59084646	AATCTTTTGTCGCAG[C/T]TTTGAAATAAACGGT	54778
rs542233691	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59033742	TCCAAACTTAATTCA[C/T]TTAAAAATCTTATTT	54778
rs542270642	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59031734	TGAGTAAAACATGGA[A/G]CCTATTGCATTGCAT	54778
rs542277479	snp	A/C	0.00597247	0.0543191	intron-variant	RNF111	GRCh38.p7	15:58997826	TCTCAAAAAAAAAAA[A/C]AAAAACCCAAAAAAT	54778
rs542340286	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59053687	CGTGCATAGTGCTTG[A/G]TACAACATTGACTCA	54778
rs542344972	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59089854	TGTGTAGGACTGCTA[C/T]AGTGGCTGGGAATCA	54778
rs542382492	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59046014	CCACTTCAAATATTT[A/T]CACATCTCATAACTC	54778
rs542404892	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58999271	AATGTATAGCATTAC[C/T]GCTCTTATTAAAGTT	54778
rs542406641	snp	G/T	0.00358779	0.0422022	downstream-variant-500B	RNF111	GRCh38.p7	15:59097637	GTAATCCCAGCACTT[G/T]GGGAGGCTGAGGTGG	54778
rs542434594	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59088354	GGGATGCAGGAGTTC[C/G]TTTCCGATTTCTTTG	54778
rs542446014	snp	G/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59009492	TTTCTGATCTGAAAT[G/T]ATCAAATTCTAAAGA	54778
rs542469036	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59058884	TAAAGGATATTATCA[A/C]GACAGTGAAAGACAG	54778
rs542492639	snp	A/G	1.67371e-05	0.0028928	intron-variant	RNF111	GRCh38.p7	15:59052259	TTCTGCCTAACGATT[A/G]GCTGACAGGAAGATG	54778
rs542505850	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59056056	CAATACTTGATAGCT[A/G]TTTTCTCAGGAAAAA	54778
rs542510608	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59078742	CAGGTGCCTGTAATC[A/G]CAGCTACTCGGGAGG	54778
rs542524315	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59057524	GTGACTATGCTTTGG[A/T]TGGATTTATTCCTAC	54778
rs542544084	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59064257	AGTAAATAATCTGGC[C/T]GGGCGTGGTGCCTCA	54778
rs542558031	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	RNF111	GRCh38.p7	15:58985884	AGGGGAGGGGAGAGG[A/G]AGAAGAGGAGGGAGT	54778
rs542574311	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59027779	CTCAGGTGATCCACC[C/T]GCTTCAGCCTCCCAA	54778
rs542584132	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59063354	CACGACTTTATTATG[A/T]GTAAGACTGTTGAAT	54778
rs542610209	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59034396	AGTTTGCATTAAATT[A/C]CTCGATGCTAATGTC	54778
rs542629032	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59022974	GAAATTGGCTGGGCG[C/T]GGTGGCTTACGCCTG	54778
rs542667637	snp	A/C			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020971	GTGTTTGGTTACATG[A/C]ATAAGTTCTTTAGTG	54778
rs542673142	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58992901	CTGGACATGGTGGTG[C/T]ACACCTGTAGTAATC	54778
rs542679657	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59039914	TAGAGACGGGGTTTC[A/C]CCGTGTTGGCCAGCA	54778
rs542687287	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59076558	TATTCATTTGATGCA[A/G]GCAATTAAAATATAA	54778
rs542738601	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59069437	CTCATTTACAGAATA[C/T]TTTGTTATTAATAAA	54778
rs542765693	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59037656	AGCCTGACCAACATG[G/T]AGAAACCCCGTCTCT	54778
rs542773465	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59005671	GATTGAAGTCGTACC[-/A]AAAAAAAAAATGTAT	54778
rs542803137	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59041588	AAATTACTGCAATAA[A/G]TAGCTTTTTGTATAT	54778
rs542834119	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59008966	TTTTATTTTATTTTA[C/T]TTTATTTTTTTGAGA	54778
rs542864593	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59018326	GCCCTATTCTGTCAT[C/T]AAGGTGTCCAGGATT	54778
rs542868840	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59071068	TTTGGGAGGCTGAGG[C/T]AGGCGGATCATGAAG	54778
rs542872744	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59037930	AGAGAGCTTAAGTCA[C/G]TCCCATTTTACCACT	54778
rs542874392	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59044162	CAGCCTCATGAGTAG[C/T]TGGGATTAGAGGCAC	54778
rs542902777	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59045377	TGCATTTTTAGTAGA[A/G]ACGGGGTTTTACCAT	54778
rs542905607	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59051768	CAGAGTGAGAAACTG[C/T]CTCAATAAATAAATA	54778
rs542916498	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59002082	TCATAAGCGGTTAAA[A/G]CTTGTGAGCTGTTTA	54778
rs542937778	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59043642	AAAATGCTACAGTGA[A/G]CATTTGGGTACAAAT	54778
rs542998716	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021171	TTTTTGTTTGTTTGA[A/G]ATGAAGTCTTGCTCT	54778
rs543081361	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59090438	TTTTGCCATGTTGGC[C/T]AGGCTGCTCTTGAAC	54778
rs543087551	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59026475	GTGTGTAACAGCAAG[A/C]CATTTATAATGTCAC	54778
rs543102986	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59093132	ATTAAAGTATCTATG[C/T]TACCAACATGGGAGT	54778
rs543129977	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59019485	GAAATGAGGTCTCTC[A/G]CTCTTTACTAGGATT	54778
rs543130335	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59013375	TTTCATTGTAGACTC[G/T]GGTTTCACAGTTTCT	54778
rs543163458	snp	C/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59082705	AGAACATACGGCCTG[C/T]AGAGCTGAAAAAATT	54778
rs543168536	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59019048	CCCACCTCAGCCACC[C/G]GTGTAGGTGAGACTT	54778
rs543172312	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59032644	CAGGTTGGTCTTGAA[A/C]TCCTTAGCTCAGGCG	54778
rs543174474	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59074945	TGTTGTGTCTCAGGG[A/G]ATAGGGAGGCCCAAA	54778
rs543184417	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59093162	TGGGAAATATACTGC[C/T]TATTGTAGGGCCACA	54778
rs543196851	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59016568	AATTGAGCATATACC[A/G]TATTAGTCAACATTT	54778
rs543199523	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59030112	ATAGATTAGCTGTAC[A/G]AAGTTTGATTTTATG	54778
rs543220378	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58996530	AGGTTGCAGTGAGCC[C/G]AGATCATGCCACTGT	54778
rs543308250	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58995890	CATGGAACCCTGGTT[A/C]CTTTTAGTGAGCAAT	54778
rs543331296	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59024600	TTTTACATATTTATG[C/T]GCATTCTCTTTTTTG	54778
rs543385727	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59080762	CATAAGATATCCAAG[A/T]TTATTGTAAGAAGGG	54778
rs543390705	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58988817	TTGTGTTGTTGTAAG[C/T]TTTCCTGTTTCTTGA	54778
rs543399426	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58994318	TGCTGGGATTACAGG[C/T]GTGAGCCACCACGCC	54778
rs543399793	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59086611	TAGAGGCACTGCAGG[A/G]AAGCTTTCAGAGAAG	54778
rs543409169	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59073098	GGATTGCTTGAGCTG[G/T]GTAGGTGGAGGCTGC	54778
rs543472266	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59079296	AAAGGATAGTTAACA[A/G]TCATAAAACATAGTG	54778
rs543485306	snp	G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59000470	TAATTGCAGCACTTT[G/T]GGAGGCCGAGGCAGG	54778
rs543550032	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59061738	TCTTCCTTGTGTCTT[C/T]GGCATCTTCTCTGGT	54778
rs543593214	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59040280	CCATCTTGCTCCACT[A/C/G]ATTTTTAAATTATAT	54778
rs543601821	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59091962	TCCAGCAGTGATGCT[C/T]GCTCACCTGCCACTC	54778
rs543628016	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59091261	CATTTTTATTGAAGT[A/G]ATGCATACATATTGT	54778
rs543638204	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58997198	CTTATCTTCCTATGA[C/T]CCAAGTCTTTTCTCT	54778
rs543679608	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59073324	TACTAAAAATACAAA[A/C]ATACAAAAATTAGGT	54778
rs543680411	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59037827	GGCAACAAGAGTGAA[A/G]CTCCCTCTCAAAAAA	54778
rs543681381	snp	A/G	3.29533e-05	0.00405901	synonymous-codon	RNF111	GRCh38.p7	15:59031293	TGTGACTTCAGATGA[A/G]GATAAAGAAGTCTCT	54778
rs543690406	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59047992	GTGGAGAACCTGAAA[C/T]CTTCATTTCCCTATT	54778
rs543756320	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59079957	AATACTTACAAGTCA[A/G]TAAGAAAAAGGTGAG	54778
rs543759429	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59054113	GCTAATTTTTTTTGT[A/G]TTTTTAGTAGAGACG	54778
rs543761119	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59029331	ATCCTTGTCTGACTG[A/G]CTGCCTTCTGTAATT	54778
rs543796622	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59075228	GCTTGACACAGTGTC[A/G]CCACAAACCTTCAAT	54778
rs543834523	snp	C/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59094095	CTTTATTTCTCAATT[C/T]CTAATTGGTAATTTG	54778
rs543883820	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59036650	ATTCAAGGTGAGATT[G/T]GGGTGGGGACAAAGC	54778
rs543895418	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59042328	GATGAGGTTTTGCCA[C/T]GTTGCCCAGGCTGGT	54778
rs543915719	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59048889	TGAGCCTAGGAGTTC[A/G]AGACCAGCCTGGGCA	54778
rs543925060	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB, utr-variant-5-prime	RNF111	GRCh38.p7	15:58987627	AGGCGTGAAGGCTAC[C/T]GCGCTCTCACTTTCC	54778
rs543929472	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59042223	CCTCAGCCTCCCACG[C/G]TTAAGCAATCCTCCC	54778
rs543954857	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59041821	GGGTTTTTGGTCCGT[C/G]TGATAGCTGAGAAAT	54778
rs544021471	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59071724	AGTTTTTGGAGGAAA[A/G]TATTACTGATGAGTG	54778
rs544031006	in-del	-/AGTT	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:59018764	CATACTTTCCATAAC[-/AGTT]TGTACAAATCCTGCC	54778
rs544034722	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59078002	GTTCTTAAACCTTTT[G/T]TCATCCAGAATGAAC	54778
rs544057808	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59047134	GGCCAGGAATTCTTA[C/T]AATTCAACAATGAGA	54778
rs544059768	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59040267	ACTACAGCACATGCC[A/G]TCTTGCTCCACTAAT	54778
rs544113853	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59047436	GGAGGTCAAGGCTGC[A/G]GTGAGCTATTATCGT	54778
rs544121496	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59046818	ATATTTGCAAATAGT[A/G]TATCTGAGAAAAGAC	54778
rs544182228	snp	C/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59023796	ATCAGTTTTTTTCCC[C/G]CTGAATTATGTATGC	54778
rs544257877	snp	A/G			missense	RNF111	GRCh38.p7	15:59089676	AAATAGGTTCCTGAT[A/G]TGGCAGGCTATCCTC	54778
rs544266076	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59023322	TGCTATTATTTTGGC[A/T]TGAAATTGAATTTCC	54778
rs544311951	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59053165	TCCTTCACTCAGTAA[G/T]TTTATCGGTGCTCTG	54778
rs544358521	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021844	TTGGTTATTGCTATG[C/T]GTTCATTTTTTCTAG	54778
rs544375723	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59058854	ACTTCATCAAAATTT[A/G]GAACTTTCGTGCATT	54778
rs544380630	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58992081	GATGGAGTTTCCCTC[A/G]TTGCCCAAGCTGGAG	54778
rs544404755	snp	A/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58999196	ATAAATGGAATACAG[A/T]TGCAGATGTGACAAT	54778
rs544448916	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59027590	CTGGAGTGCAATGGC[A/G]CAATCTCGGCTCACT	54778
rs544470423	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59005004	AATCAGTGAGCAGAA[A/G]GGCAAGCATAATCTC	54778
rs544494632	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RNF111	GRCh38.p7	15:58985823	ACTTAAAGCACTTCT[C/G]AATTATTTTTATTTA	54778
rs544519305	snp	A/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59059643	TAATCCAGGGTCACA[A/G]AAATTTATTCTGGAG	54778
rs544527667	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59083467	TGCTTGAATCTGGGA[C/G]GCAGAGGTTGCAGTG	54778
rs544537415	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58991353	ACATTTTAAAGAGCG[G/T]TACTGCATTATTACG	54778
rs544557881	snp	G/T	0.0111196	0.0737302	intron-variant	RNF111	GRCh38.p7	15:59090244	TTTGTTGTTGTTGTT[G/T]TTTTAGATGGAGTCT	54778
rs544609177	snp	C/T	4.95765e-05	0.00497853	synonymous-codon	RNF111	GRCh38.p7	15:59084219	GCCTCAGACTATGTC[C/T]TCACATCCTCGACAG	54778
rs544622250	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59089007	AAACAAGACACTGGT[G/T]TATAGTAGGAGCTCA	54778
rs544627189	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59076456	GTTGAGTAGTATTTC[C/T]AGGCACAGTAAAGTA	54778
rs544642566	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59037086	AAGTGATGTGCCTGC[C/T]TCGGCCTCCCAAAGT	54778
rs544668965	snp	A/G			synonymous-codon	RNF111	GRCh38.p7	15:59085662	TCCTTTCGTTAGGGA[A/G]CTGGGAATTGAAGCT	54778
rs544675991	snp	A/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:58996863	AGTCAGTTTCAAAAG[A/T]CTTACAATGAAAAAC	54778
rs544677890	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59002758	ACTACTTCTGATGTC[A/G]TTGTGTGCCATTTCC	54778
rs544699427	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59058274	TTTTATTTATTAATT[A/G]TAAACACATTAGCTT	54778
rs544713820	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59016097	CCACCTTGGCCTCCA[A/G]GAGTGCTAGGATTAC	54778
rs544714955	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59002330	TTCAGGTTTTTCCTT[C/T]AGAATTAATAGCTGT	54778
rs544732999	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59088043	AGGGAAAGTGAAGGA[A/G]ACCCCTATTTGGTTG	54778
rs544796353	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59095980	CTCTTGTTTTATTTC[C/T]CTCTAAACTTGAAAA	54778
rs544806880	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF111	GRCh38.p7	15:59094905	GTGAAAGTTGACACC[A/G]TGTTTCAGAACTCTT	54778
rs544809672	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59081468	GGGCAACACAGTGAA[A/T]TACTGTTTTTTGTTG	54778
rs544812593	in-del	-/A	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59058076	TGTGATAGATCAGAC[-/A]ACTTATTTAGAAGCT	54778
rs544833646	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59092356	GAGGGTCTTAAAAAT[A/G]TACTTAATTGATGAT	54778
rs544835325	snp	A/G	0.00438332	0.0466095	intron-variant	RNF111	GRCh38.p7	15:59071481	TGACCGCAAGAGTTC[A/G]AGACCACCCTGTGCA	54778
rs544871388	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59015080	TGTTATTTTAAAATT[C/T]TGTAGTTTGGCCTTT	54778
rs544873424	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59047814	TCCTTAGCTCGAGCA[A/G]TCTGCCTGCCTCGGT	54778
rs544881406	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59034371	GTTGTTACCAGAATG[C/T]CCTCCAAGAAGTTTG	54778
rs544908681	snp	G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59063600	CTCTAATTTATGACA[G/T]TTTTATTTGGGTAGT	54778
rs544909228	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59057455	GTATAGAAAGTCAAC[C/T]CTCTCATTCCATAGC	54778
rs544933802	in-del	-/G			intron-variant	RNF111	GRCh38.p7	15:59023056	GTTCGAGACCAGCCT[-/G]GCCAACGTGGTGAAA	54778
rs544936487	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990952	AGGTTTCTACAGGTA[C/T]TCAATTTATATCATT	54778
rs544948511	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59075763	TTTTCACAATCCAGG[A/G]TACACTTGTTATATT	54778
rs544957175	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59033432	TCATTTTGATCATGT[A/G]CAGCCAGGTGAGAGG	54778
rs544982863	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59056501	CACTCATAATTTCCC[A/G]AAAGGAAAATGGTAA	54778
rs544995339	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59014052	TTCCATGGCCTCCCA[A/G]CATGCTAGGATTACA	54778
rs545007114	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59001039	TAATGTTGGTATTAA[C/T]TACTAATGTGAGGTG	54778
rs545011865	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59082043	TGATCATGCCACTGC[A/G]CTGCAGCCTGGGTGA	54778
rs545023784	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59033684	TAATTGAATGTCATT[A/G]TCAGTGCCAGGGGTT	54778
rs545047475	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59061949	TGTTCTCATCCCCCC[A/T]TTCACTAGCCCATTT	54778
rs545058175	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59072607	AGGTGCCCGCCACCA[C/T]GCCTGGCTAATTTTT	54778
rs545068963	snp	A/C	0.00199481	0.0315187	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096838	GTGCCAAGGGACTGA[A/C]GAAGTGTAAGATGGG	54778
rs545078940	in-del	-/T	0.00597247	0.0543191	intron-variant	RNF111	GRCh38.p7	15:59011333	AGTGATATTTCTCAC[-/T]TAACTGCTAGACTAT	54778
rs545083425	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59045337	CTGGGACTACAGGCA[C/T]CTGCCACCACACCTG	54778
rs545086482	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59068066	CTTTAACTTTTGTTA[G/T]GTCACTTCCATGTAC	54778
rs545105658	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59093749	ACCTTGTAGTAATAT[G/T]ATTGCCCTAATTTAT	54778
rs545144578	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59074159	TGTTGTTTGTTAATA[C/G]AGCACAGGCAGAATA	54778
rs545158619	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59073598	TTCCAACTTCTTATT[C/G]TAGTTCTCTTGCTGT	54778
rs545165788	snp	G/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59064393	ACAAAAAAATTAGCC[G/T]GGCTTGGTGGCGGGC	54778
rs545185125	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:58993116	CAGAGGTTGCAGTGA[G/T]CCAAGATTGCGCCAC	54778
rs545186946	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59008438	TGCCCAGGCTGGTCT[C/T]GACTCCTGAGCTCAA	54778
rs545213559	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59080615	TGCAGGAGTGAGCAT[A/C]TACACAGATATTTAT	54778
rs545241359	snp	G/T	0.000395713	0.0140606	missense	RNF111	GRCh38.p7	15:59031373	CACGGTCTCATAAGT[G/T]GCCTCGGACTGAGAC	54778
rs545248045	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59049572	GTTTTGGGAAGCCAT[A/C]TCAGCTGTAGTGCTT	54778
rs545252552	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59043023	TATGGGATGTCTTCA[C/T]TTGTTGATGTCTAGT	54778
rs545257403	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59051181	ATTTTGCGCCTGGTG[A/C]GGTGGCTCACGCCTG	54778
rs545294679	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59080077	ATTTTAAAAATTTAG[C/T]GGTAATGTGGGGGTA	54778
rs545319842	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59037556	AAATTAATAGGTATT[C/G]CCGGGCGTGGTGGCT	54778
rs545343270	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58995144	CTCATCAGATCATCC[C/T]GTTCCTCATCACTCC	54778
rs545404256	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59086047	CTCTTAATCCACTGT[C/T]AGGAGTATACTGTGC	54778
rs545428035	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59049094	TCTCACACACACACA[A/C]AAAAGTATATTTACA	54778
rs545460800	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59082874	ATAGTAACCTTTTAT[A/G]TAGAAAATTGCCAGT	54778
rs545462454	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59026015	GATTACAGGCGTGAG[C/T]CACTGTGCCCGGCCG	54778
rs545508059	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59028707	ATAAGTTTTTTTATG[A/C]ATATGTGTTTTCATT	54778
rs545512495	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59012712	GGTTTTAGGCCCTTT[C/G]TTTTCTCATGGTGGT	54778
rs545563141	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59037856	AAAAAAGTAGGTATT[A/G]CAGATTATATCTCCT	54778
rs545590128	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59060711	AGTTAAGTACCTTGA[A/C]AAAACTGTAATAATT	54778
rs545599439	snp	A/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59001569	TTTACCAGGAAAAAG[A/T]TATATTAGTGACATG	54778
rs545600266	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59018486	AAATTTAAATATATT[A/T]TGTTCTCATAATTTA	54778
rs545639672	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59030589	TGCTCTATATCTACT[C/G]TATTTCTAAAAATTG	54778
rs545676562	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59029931	ATGTTTTGCACTAGT[A/G]AAGCTCTTCATTTGT	54778
rs545700335	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59033330	TCTCTTTTTGCCAGA[A/G]CCCTAAACCAGTAAC	54778
rs545721996	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59007150	TTGCCAAATGCATCT[A/G]TTTATTGCCCAAATC	54778
rs545774485	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58999849	GAGCTTTTACTCATG[G/T]TAGAGGGCAAAGCAA	54778
rs545783699	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59013331	AGACCCACATTGATA[C/T]ATCACTGTTAAATAA	54778
rs545805445	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59093033	AAGTAAACTGGAAAC[C/G]AAATAAAGATTACTT	54778
rs545812316	snp	G/T	1.66663e-05	0.00288667	missense	RNF111	GRCh38.p7	15:59055739	GGGTTCCAGTTCTCA[G/T]GCAAGTCGGCCACAG	54778
rs545898002	snp	C/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59040206	TTGCAGACTTGACCT[C/G]CTGGGCTCAAGTGAT	54778
rs545899683	snp	A/G	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59005248	CCTAGGCTGATCTCA[A/G]ACTCCTGGGCACAAG	54778
rs545918981	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59041747	ATTCTGAATGCTCAC[C/T]GGCAAGGGTGCCTGT	54778
rs545977800	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59090383	TACAGGTGCCCGCCA[C/G]CACGCCCGGCTAATT	54778
rs545997775	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58988739	TTTTGATTATTCAAA[A/G]AATACCAGAAAGTAT	54778
rs546044844	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59036497	AGAGAGAGCTTGTGC[A/G]AGGAACTTGGCATTT	54778
rs546074633	snp	G/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	RNF111	GRCh38.p7	15:58988154	GGAGGGGAGAAAGAG[G/T]AAGGGCTGCGGCCGC	54778
rs546117763	snp	C/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59017236	CTGCTGTGTAGGCCA[C/T]GATAATTTTTATTTT	54778
rs546128668	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59079191	ACTCATTCTGAAACA[A/C]AACTTCTTGCTTTGT	54778
rs546164654	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF111	GRCh38.p7	15:59097246	GTAGCTGTCCAAATA[C/T]ATAAAAACTAAAATT	54778
rs546176708	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58991264	ATCTGCACTCCAGCC[C/T]GGGTGACAGAGCAAG	54778
rs546195401	snp	A/G	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:58997158	AAAGAATGTACAGGG[A/G]AAAAAAACAAGGCTC	54778
rs546234450	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59041327	TTGGGAGGCCGAGGC[A/G]GGTGGATCATGAGGT	54778
rs546250782	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58999399	GGAGTGCAGTGGTGC[A/T]ATCTCAGTTCACTGC	54778
rs546287376	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59011916	ATGGTTCACTACCAA[A/G]CTAGGATTGTCAAAG	54778
rs546323865	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022099	TCCTGACCTAAAGTG[A/T]TCTCCCCGCCTTGGC	54778
rs546337577	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59054042	CTGGGTTCAAGCAAT[C/T]CTCCTCCCTCAGCCT	54778
rs546349540	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59069927	GAGAAGATGCAGTAG[G/T]CATGTAGATAGCCCT	54778
rs546362864	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59064313	GGTCGAGGTGGGTGG[A/G]TCACGAGGTCAGGAG	54778
rs546399306	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59028380	TGAAACCATATAGTG[-/T]TTTTTTTTTTCATAT	54778
rs546423013	snp	C/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59018940	TCTTTTTTCTTTTTT[C/T]TGAGACAGCGCCATG	54778
rs546459755	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990676	ACAAACAAAAAAACT[A/G]TGATTGTTGTTCCAC	54778
rs546527147	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59075513	CTTGGGGCAGACAAG[A/T]TTTTTCCTAGAACCT	54778
rs546532397	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59039334	AAGGAAGAACACTTT[A/G]TTCATCAGCTCATTG	54778
rs546542326	snp	C/G	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59040246	TCAGCCTTCTGAGTA[C/G]TTGGGACTACAGCAC	54778
rs546546790	snp	A/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:58997498	TCACTATGTTCTTCA[A/T]GACTACACATTTGCA	54778
rs546569457	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59018732	ACTTACTTGTAGTCC[A/G]TTTAAAGAAAATGAT	54778
rs546593844	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59045481	GGCGTGAGACACTGC[A/G]CCCGGCCTTAGTTTT	54778
rs546618662	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59015788	ATGAAGCCATTATCA[G/T]AGTCCTTAATTGCCT	54778
rs546659458	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59058035	CATAGTAAGGAACTT[C/T]TATTTCCTTTTACTG	54778
rs546667096	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59088444	TTGTAAACAATTTAA[A/G]TAATAGGCTATTGAA	54778
rs546680463	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59051236	AGGAGGGTGGATCAT[A/G]AGGTCAGGAGATCGC	54778
rs546684408	snp	C/G	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59004520	AACCATAAAAGGTTT[C/G]TTAAATAAAGTAGCT	54778
rs546692801	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59050754	TCTTCCTGTCTCCTT[A/C]CTTTTGTTTCCTTTT	54778
rs546694588	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59057121	GCAATGTCTGCAGAC[A/G]TTTTTGGTTTTCACA	54778
rs546802278	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59014783	TTTTTTTGAGACAGG[A/G]TCTTCCTCTATGGAC	54778
rs546825573	snp	G/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59033618	GACAGGATGGTTGAT[G/T]TGGAGCAGAAGTTCT	54778
rs546836706	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59011855	AGAAGTTCATAGCAC[A/G]TTGAAACTGACACTT	54778
rs546856366	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59062629	TAACATTTATTGAGC[C/T]TATAGTGTTGGCCGG	54778
rs546867532	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59010636	TGAACTCCTGACATC[A/G]GGTGATCTGCCCACT	54778
rs546874414	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59026196	CCTCAGAGTTGTATG[A/G]ATAGTCTTAATGGGT	54778
rs546879441	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58997096	TTTTAAGTTAATTTT[C/T]TCAGAGAAAAGTAAT	54778
rs546911713	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59032971	AGTCCTGAAATGTAT[A/G]TTCCATGTATACAAA	54778
rs546961866	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59032194	TCTGCCCACCTCAGC[C/G]TCCCAAAGTGATGGG	54778
rs546971377	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59081746	AGAAAACAAAAGATA[C/G]GTGGCTGCAGTGATT	54778
rs546975313	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59087749	GGGGTGGCAGAGGTG[G/T]CAGAAAATCTACATG	54778
rs546998708	snp	G/T	0.000399281	0.0141238	missense	RNF111	GRCh38.p7	15:59031486	GTAAAAAATAATTCC[G/T]CACAGAGGACACAGA	54778
rs547032410	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58988547	TATGGAGTTGGCTTG[C/T]TGGTCATTTAAAAAG	54778
rs547070028	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58996041	TTATGAAGTAATCAC[A/G]TAAGACTCAGCAACT	54778
rs547136288	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59008096	AATCACATAAACTTT[C/T]TGCTGTGTTTTTTCT	54778
rs547177227	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59014169	AGCTTTGGCCTTTGG[C/G]AGCTCTTTCAGCTTG	54778
rs547222604	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59006930	AGCTGGGATTGCAGG[C/T]GCCCGCTACCACGCC	54778
rs547224627	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59013485	TGGAATGTTTTTCTC[A/G]TAGTTTGGGGTTTTG	54778
rs547270349	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59000687	CCGCTCCATCCTGGG[C/T]GACAGAGCTGAACTC	54778
rs547304648	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59042561	CAGTCCTTGTACTTA[A/G]TTCATTTTTAACATT	54778
rs547307351	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58997676	ACAAAATTAGCAGGG[C/T]GTGGTGGCATATGTC	54778
rs547323265	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990290	ATTGTTGTGTTTGTC[A/G]TAATTGAATCCCCAG	54778
rs547336907	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59092372	TACTTAATTGATGAT[A/G]GTCACTTAATTCATC	54778
rs547367995	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59049418	ATGAATTCACAGGTT[A/G]TAGGTTCCAGCAGTT	54778
rs547410615	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990020	CTGAAAAATGATAGC[A/G]GTTAAAATATGTTAT	54778
rs547435798	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59038215	GCTTTGTGTGAGGTA[C/T]GGCACGCACTGACTC	54778
rs547438935	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58995358	CTGTTTTATTCAGTG[G/T]GTTAAATAACCCATT	54778
rs547456409	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58988914	TGTAGGATTTCCTGT[A/T]GCTTTTGAATGTGAC	54778
rs547477231	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59001267	AGAACAGAGGTATGA[A/G]GGGTTCATGTTCTTC	54778
rs547493124	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF111	GRCh38.p7	15:58988299	AGCCTACAGTGAGGG[A/T]GTGTGGGTGAGGGGA	54778
rs547551921	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59085101	TTGTGTGTGGGCATT[A/C]ATTGAGATCTTGAAC	54778
rs547562441	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:58999461	CTGCCTCAGCCTCCC[C/G]AGTAGCTGGGATTAC	54778
rs547577791	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58993837	TTAGCATCTTAGTTT[A/G]GTTTGTATGTGATTG	54778
rs547594904	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59023218	ACACCACTGCACTCC[A/C]GCCTGGGTGACAGAG	54778
rs547615998	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58992984	GACCAGCCTGCCCAA[C/T]GTGGCAAAACCCTGT	54778
rs547642130	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59049992	TGATCCTCCTGCCTC[A/C]GACTCCCAAAGTGCT	54778
rs547707156	snp	C/T	0.00332134	0.0406157	intron-variant	RNF111	GRCh38.p7	15:59055886	AATTATGAAAGGAGT[C/T]TGATAAAAGGAAATC	54778
rs547719299	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59055106	TAGAAGCATAAACTA[A/G]CTCACGCAAGTAATA	54778
rs547732702	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59060915	CAAGTGATCCTCCCG[A/G]GTAGATGGGGGACCA	54778
rs547792979	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58999498	GCACCATCACACCCG[G/T]CTAATTTTTGTATTT	54778
rs547840733	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59037778	GAAGCAGAGGTTGCT[A/G]TGAGCCGAGATCACG	54778
rs547887351	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59053486	TATATATTCATATTT[C/G]TGACATCTGTTACAA	54778
rs547887968	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59090593	TTAGAACTATTGTTT[A/G]ATTTGGTTCCTTAAT	54778
rs547888950	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59060249	TTTGTTGAGTACATA[C/T]TCTTTTCTTAGCTTG	54778
rs547904372	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59047562	CAGCACCATTAGTTA[C/T]TTTGTGTTTTTTTTA	54778
rs547976218	in-del	-/TTTTTTTT	0.201727	0.245295	intron-variant	RNF111	GRCh38.p7	15:58996650	CTCATCAGTACTTTC[-/TTTTTTTT]TTTTTTTTTTTTTTT	54778
rs547983491	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59030113	TAGATTAGCTGTACA[A/C/G]AGTTTGATTTTATGT	54778
rs548000898	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59000056	GGAATTACACTTTGA[C/T]CTGAGATTTGGTTGA	54778
rs548021633	snp	A/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59041963	TCAGTCTGTTCATAT[A/T]TTTTTTTTTTTTTTT	54778
rs548085813	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59006157	TTGCTTTTTCTGTGT[A/G]TTCCAGATTTTATAT	54778
rs548105647	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59084773	TTTCCTCATTCATGA[C/T]CCCCCACCCTCTCCC	54778
rs548132809	snp	A/G	0.00478085	0.0486577	intron-variant	RNF111	GRCh38.p7	15:59022755	TTGGCAGATAATAGG[A/G]AACTTCTCATTATTA	54778
rs548162198	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59081649	GATAATTTGAGCCCA[A/G]GAGTTCAAAGCTGAG	54778
rs548167613	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59091351	TAGTCCTTCTTCCCA[A/G]AAGTGAAATCATAGT	54778
rs548226328	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59071290	GGCAACAGAGCGAGA[C/T]TCCATCTCAAAAAAA	54778
rs548229284	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59039919	ACGGGGTTTCACCGT[C/G]TTGGCCAGCATGGTC	54778
rs548243659	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59000033	GGCAGGCCCCACCTC[C/T]AACAATGGGAATTAC	54778
rs548247955	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59011586	GGTTTTTCCTGAGGC[C/T]CCTCTTCTTGGTTTA	54778
rs548257623	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59038857	TCAGAGGGTTCAGAT[A/G]TTGTCATTCTGATCC	54778
rs548321296	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58998178	AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACCG	54778
rs548326150	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59010886	TCTCCTGTTATTTAA[C/T]TGGAATGAATTCTGA	54778
rs548330871	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59023398	GGTCCTTTGTGTCTC[C/T]TGTTAAATTTCATAC	54778
rs548331340	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59009615	TTAGAACTTGGAGCA[G/T]TTGTGAGTGAGTGTC	54778
rs548373104	in-del	-/AG	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59075171	ATGTGACACAGACAC[-/AG]AGTTTCCACATGCTG	54778
rs548413126	snp	A/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59016154	TTTTGGTTAAAAAAT[A/T]TATATATGTATATAT	54778
rs548415484	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59009336	TTCATCTTAGCTAGA[A/G]CATAGTCTTTGTGAG	54778
rs548449845	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59015719	AAGTGAATATTCTTC[A/G]CCCACCGTCACCCTG	54778
rs548477002	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59079633	CCAATAAAATGAAAT[G/T]TGTATTGAAATCTAA	54778
rs548512374	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF111	GRCh38.p7	15:58986539	TTTTTTTCTTGGAGA[C/T]GGAGTCTCCCTGTCA	54778
rs548603794	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59026353	TAGTGGTGTATTCTA[C/T]ACTAGTATCAGGAGT	54778
rs548617777	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59083526	GGTGACAGAGCTAGA[C/T]TTCCTCTCCAAAAAA	54778
rs548617859	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59076708	CTATAAAAATAAAAT[A/C]GAACCAGCCATGCCT	54778
rs548668158	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021323	GCCCGGCTAATTTTT[A/G]TATTTTTAGTAGAGA	54778
rs548671232	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990633	CACTCCAGCTTGGGC[A/G]ACAGAGCGAGACTGT	54778
rs548679738	snp	C/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59086032	TTGTATACCAAGATA[C/G]TCTTAATCCACTGTC	54778
rs548717312	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59003288	CAGCTAAGTTTTTGT[A/G]GAGACATGCTTTTGC	54778
rs548723881	snp	G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58993405	TAGCTGGGCGTGGTG[G/T]TGGGTGCCTGTAATC	54778
rs548727073	snp	C/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59083019	CTGGGTATGGTGGCA[C/T]ACACCTTTAGTCCCA	54778
rs548775260	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59088652	TCTCACTATGCATGG[C/T]AGTTATGATCTATAC	54778
rs548785628	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59069847	CTGAGATTTGTGATT[C/T]TGTAGATATCTTATG	54778
rs548791602	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59045669	ACTTGTCGTTGATAC[A/G]TAATGCTTTTAGTTT	54778
rs548864584	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59028815	GATAGAGTCTTGCTC[C/T]GTTGCTCAAGCTGGA	54778
rs548893372	snp	G/T	1.65083e-05	0.00287296	missense	RNF111	GRCh38.p7	15:59080993	GCCCGCATTCTCATG[G/T]AAACCCCCCTCCTCA	54778
rs548900853	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59057894	TGGTTAAATAACTTA[C/T]TTATATTCATACTGT	54778
rs548900999	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59053726	GAGCTGTAAGGACTA[C/T]TGAAATTACAGACCT	54778
rs548926763	in-del	-/G	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:59026035	TGCCCGGCCGGCTTT[-/G]TTTTTTTTCTTTTAA	54778
rs549006528	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59044509	CTCGCAGAGAAACCA[C/T]TGTTTTTGTTATCAT	54778
rs549017009	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59051217	CCAGCACTTTGGGAG[C/G]CTGAGGAGGGTGGAT	54778
rs549020887	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59008499	CTGGTATTTACAGGC[A/G]TGAGCCACCGCACTC	54778
rs549069106	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59062014	GCTGATGACTCTCTC[G/T]TCTGTGTTTTTTGAC	54778
rs549088630	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59033560	CATATACTAGTTTTG[G/T]GAGTGAGTACAGCAG	54778
rs549104133	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF111	GRCh38.p7	15:59094985	GGCATGACTTACCTG[C/T]GCAGATTTGGAAGCA	54778
rs549104682	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59069006	TTGAACGTGGGAGGC[A/G]GAGATTGCAGTGAGC	54778
rs549132397	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59061489	ATTTCAAAACACTCT[C/G/T]CTTTTCCTCAAGGTT	54778
rs549158135	snp	A/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59034251	TGGATATTTGCTGCA[A/T]TGAGCAACATTGTGC	54778
rs549197079	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59043096	TTGAGGTATAATTAA[A/C]TACTATAAAATTCAT	54778
rs549210738	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59056029	ACATAAAATTCTTTG[C/T]GGTTATTGTTTCAAT	54778
rs549220670	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59087959	GCACCTCTTAGATTA[A/C]GTACGGTAAGGAAGT	54778
rs549235997	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59039005	GTTTCACTTTTGTTG[C/T]CCAGGCTGGAGTGCA	54778
rs549271130	in-del	-/TCT	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59084933	ATCTTACTTTTCACA[-/TCT]TCTTTATCTGACCCC	54778
rs549275837	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59026030	CCACTGTGCCCGGCC[A/G]GCTTTTTTTTTTTCT	54778
rs549276604	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59001843	CCAAGACCCCCAGTA[G/T]ATGCTTAACAGCCAC	54778
rs549289626	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59037591	CCTGTAATCTCAGCA[A/C]TTTGGGAGGCCAAGG	54778
rs549302557	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58989516	TATCACGGGTGCTAT[A/G]TCATGTGCAGATCCT	54778
rs549315126	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59008052	ATGGTAGTACTTTCT[A/G]TATCCTGTGAAATCT	54778
rs549430709	snp	C/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59067678	ACTTTTTAAAAAGGC[C/T]TTTGATGTTTTTAGT	54778
rs549465305	snp	G/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59073269	CACTTGCGGTCAGCA[G/T]TTCAAGACCAGCGTG	54778
rs549475997	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59019783	GGCCAACGTGGTAAA[A/G]CCCTGTCTTTACTGA	54778
rs549527054	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59079774	TGTAGAATGAAGAAA[C/T]GGTAGGAGCCATCTT	54778
rs549555559	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59074335	AAAGTCCTGGATGAC[A/G]TCTTCCAATATTAGG	54778
rs549608144	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59018537	TTTCAAAATTGGTAA[A/G]TGGTTACTTTTTAGA	54778
rs549615960	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58989819	TTTACTTTAAAATAA[A/C]AAATATAAAGGAAAC	54778
rs549645036	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59018131	CTTTTAATGAAGAAA[G/T]ATTTTGTGAAATGGT	54778
rs549661712	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59006347	AAAGTTCCTTTGTGC[A/T]CTTTTGCCATCAGCC	54778
rs549682373	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59048349	AAGGAGCCAAAAGTG[C/T]ATGCAATGTGTGACT	54778
rs549692913	snp	A/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59051799	AATAAATAAATAAAT[A/G]AATAAATGAATAAAT	54778
rs549699097	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58995322	ATTCTTTTATCTGAT[C/T]AATACAGAATTGTGT	54778
rs549732594	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59024130	GAAGAAGGAAATTGA[A/G]CAATAGTAAATTTTC	54778
rs549747961	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59012199	GATTTTTGTATTTTT[A/G]GTAGAGACACAGTTT	54778
rs549753506	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59080151	TTTGAGGTGGAGTCT[C/T]ACTCTGTCGCCCAGG	54778
rs549792112	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58994568	CTGTAACCTCCATCT[C/T]CCAGGTTCAAGCGAT	54778
rs549792793	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59054386	TCCATCTAGTACAAT[A/G]TGATGCTTTCACAAA	54778
rs549822575	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59086122	GTCATACTTGATTTT[A/C]TTTTTTCTTTTTTTT	54778
rs549824380	in-del	-/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59084051	TATTAATACTAGGGA[-/T]TTTTTTTCTACATTA	54778
rs549856893	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59076973	TTGGATTTTTTCTTC[C/T]ACTCCAGTCATTTAA	54778
rs549858709	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59049222	TACCACCACTCTTCT[C/T]TCTGTTTCTACAAAT	54778
rs549862787	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59006882	ACCTCCGCCTCCCGG[A/G/T]TTCAAGCAGTTCTCT	54778
rs549951733	snp	A/G	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:58999429	CAATCTCCGCCCCCC[A/G]GGTTCAAGCAATTCT	54778
rs549980798	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59084362	ATGATGTGGAGAAAC[C/G]TAATCCCCAGTTTAA	54778
rs549981293	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58987861	AACCCACGCCGGCTT[A/G]GCTGGGCCGAGTCCA	54778
rs550034278	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59035445	GTAAAATTAGAAGCA[A/G]GTTAGTTCCTAGATG	54778
rs550071090	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59053118	TACTGTGTTAGGGCA[C/T]CCTAATTCAAAACAT	54778
rs550083743	snp	G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59060817	TTATTATTTTTTTTT[G/T]TGTGAGACAGGTCTG	54778
rs550094329	snp	G/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59090418	TATTTTTAGTAGAGA[G/T]AGTGTTTTGCCATGT	54778
rs550124314	in-del	-/GTG	0.00993419	0.0697739	intron-variant	RNF111	GRCh38.p7	15:59013845	CCAGGCTGGAGTATA[-/GTG]GTGCTTTCTTGGCTC	54778
rs550146421	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59060090	TTGGCCCAGGCCAGT[C/G]TTGAAGTTCCAGGCT	54778
rs550149981	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59068757	AAAATTTTGATGGTA[C/T]GTCTTCTGGGTCTGA	54778
rs550152466	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59030033	TGTACATTGCATTGA[G/T]GTAAATGCTTTAAAT	54778
rs550168698	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59072627	GGCTAATTTTTTTGT[A/G]TTTTTTAGTAGAGAC	54778
rs550198093	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59084463	CAAGCAGGAGTAGTA[C/T]TTTTTTTAGGTGTTA	54778
rs550207593	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59036111	ACAGTCTTACTCTGT[A/G]GCCCAGGCTGCTGGA	54778
rs550216420	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59070316	GAAGAGGGTTCTCAT[G/T]ACTGTTTTTATTTTC	54778
rs550222667	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59004548	GCTGACATCAGTATG[C/T]AGGATAATGAATTCT	54778
rs550259460	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59010549	TGGGATTACAGGTGC[C/G]CACCACCACACCTAA	54778
rs550277533	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59065726	GAAAAAAGATAATGG[C/T]CCAGACATGGTGGCT	54778
rs550286643	in-del	-/CATTTTCTTCCC	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59061915	CTCCTTTTCATAATT[-/CATTTTCTTCCC]AGGACTGTGTTCTCA	54778
rs550343012	snp	G/T			utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58987770	GGCGACGGCGAGGAG[G/T]TGTTCGGTTTGCGCA	54778
rs550360477	in-del	-/TTTT	0.00993419	0.0697739	upstream-variant-2KB	RNF111	GRCh38.p7	15:58986907	GGGAGGGAATTAATG[-/TTTT]TTTAGTGAACACTTA	54778
rs550363851	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59035099	AGATTGTGCAGGGGA[A/G]CTCCCATTTATAAAA	54778
rs550367935	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59077734	TGTGATTGCTATGTC[A/T]GAGGGCTAAACTTTC	54778
rs550376143	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59005430	CTTATTGGACTTCAT[A/T]CAAAGAGAAATTGTT	54778
rs550381497	snp	G/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59064258	GTAAATAATCTGGCC[G/T]GGCGTGGTGCCTCAC	54778
rs550389978	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59059028	CATGCTTGTAATTCC[A/T]GTACTTTGAGGGGTT	54778
rs550423054	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59071897	CAATAAAGCAAGTCA[C/T]ATGAATTTTTTTGTT	54778
rs550432138	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59041457	ACTCAAGAGGCTGAG[G/T]CAGGAGAACTGCTTG	54778
rs550451711	snp	C/T	0.00517822	0.0506191	intron-variant	RNF111	GRCh38.p7	15:59069161	ATTGAGTAGAAAATA[C/T]AATTAAAGAGATTTT	54778
rs550464662	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59011421	CATTCTAGCACATTT[A/G]AGGTACTCAGAAAGT	54778
rs550477935	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	RNF111	GRCh38.p7	15:58986417	AGAGACAGCGTTTCA[C/T]CGTGTTAGCCAGGAT	54778
rs550492795	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59047490	TTGGATCAAGACACT[C/T]TCTCAAACACAAACA	54778
rs550494400	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59040832	TTTCACATGCATTTA[C/G]GTTCATTTATTTCAG	54778
rs550504581	snp	C/G	0.00438332	0.0466095	intron-variant	RNF111	GRCh38.p7	15:59027933	CTGGTTCAAGCAATT[C/G]TCCTGCCTCAGCCTC	54778
rs550569949	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59062134	CTGCAGCCTCCACTT[C/G]CAGGCTTAAGTGATC	54778
rs550589362	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59009833	TGATGGCTCATGTCT[C/G]TAGTCCCAGTTACCT	54778
rs550592330	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59034161	ACTATGTATAGTTAT[C/G]TCATTCTTCTTGACA	54778
rs550595599	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59039477	TTTTCACTTTTGAGT[A/C]TCATTATGAATGCAT	54778
rs550595651	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59046190	ATTTGCTGCTTTTTT[C/T]TTTTTTTCCCTTTAA	54778
rs550632909	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59076674	AGACCAGCCTAGGCA[A/C]CATAGTGAGACCCCG	54778
rs550635652	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59052880	GAGTTAATGCTCTGA[A/G]TAAACAATAATTTTA	54778
rs550657365	snp	A/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59033967	GATTTAATAACATTC[A/T]CACGATATGGAATTT	54778
rs550671225	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020759	TTAGGGGGCTGAAAC[A/G]TCCAGCTACCAAACT	54778
rs550676881	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59016326	AGGCACGCACCACCA[C/T]GCCCAGCTGATTTCT	54778
rs550681789	snp	C/G			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986266	CTGTCGCCCAGGCTG[C/G]AGTGCAGTGGCACAA	54778
rs550694025	snp	C/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59082913	CTTATCTTCCAGTAA[C/G]TGGCAAATTGTTGTT	54778
rs550698702	snp	A/G	3.29462e-05	0.00405857	missense	RNF111	GRCh38.p7	15:59058490	AGTAGCCAACCTTCC[A/G]CAGTGTCAGAGACTT	54778
rs550803769	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59052017	ACAGGATAAATATCT[A/G]TATAAGATCTTACAA	54778
rs550808259	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021235	GGCTCACTGCAAACT[C/G]CGCCTCGTGAGTTCA	54778
rs550854789	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59015604	CTCTGATAATTTGAC[C/G]CTAGCTTATTCTCCC	54778
rs550864870	snp	C/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59057727	AAGGCATGGAAAGGA[C/G]ATTAAAACAGTTATT	54778
rs550901104	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59083293	TGGCTCATGTCTGTA[A/G]TCCCAGCACTTTGGG	54778
rs550905216	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58998107	ACGTGGTTTCACTAT[A/G]TTGGTGAGGCTGGTC	54778
rs550926248	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59056624	TAGAGGCCATATACA[A/G]TCAGCTCTTCTATGG	54778
rs550929219	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59026611	ATTTAGAATATTATC[A/T]GTTATATTTGCTGCT	54778
rs550958810	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59082271	TTATGCAAACCAATT[A/T]AAAAAAAGTACCCAG	54778
rs550990995	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59003718	ATTTTCTTAATAGCA[C/T]GTGTTTCGCTCTAAA	54778
rs551029856	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59003044	GGATTGCAGTTGGCT[A/C]TTCACAGGTGCTATT	54778
rs551062588	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59088509	ACATATGAAGTGTCC[A/G]TTAAAGCTATAAATT	54778
rs551109313	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59002544	AAAGCCCTCATAACT[A/G]TGCATTTAATTAAAA	54778
rs551110529	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59075103	TCATCAAATATCACC[A/G]TAACAGATAAAATAA	54778
rs551128150	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59051390	GTGAACCCAGGAGGC[A/G]GAGCTTGCAGTGAGC	54778
rs551150479	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59017496	CCATCTTTTCTGTAT[A/G]TTTATAAAAACATCA	54778
rs551167251	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59071511	AACATGGTGAAACCC[C/T]GTTTCTAACAAAACG	54778
rs551175433	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096520	CTCAAATTGACATTT[A/G]CATAATTTGACATTT	54778
rs551189836	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59087830	TGTAATATGGTCAGT[A/G]TGGTGTCATCACAAA	54778
rs551195641	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59005023	AAGCATAATCTCCTA[C/G]ATGGTTTAAATTATT	54778
rs551196769	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59014841	GCTCACTGCAGTCCT[C/T]ACCTCCTGGGCTCAA	54778
rs551197109	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59001291	GTTCTTCAGTTATAT[G/T]AAATATTTACATTGC	54778
rs551247308	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59067527	TCACATTCTTACACT[C/G/T]GAAAATGGCCTAATT	54778
rs551257211	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59008042	TTTTTAAGAAATGGT[A/G]GTACTTTCTGTATCC	54778
rs551264998	in-del	-/AGG			intron-variant	RNF111	GRCh38.p7	15:59070629	GTACAGCTCAACAGA[-/AGG]AGAACAGACATATAC	54778
rs551285272	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59007459	GCTGTATAACATAAT[A/T]TATCCATTCACTTGG	54778
rs551286206	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58995482	TTTTTTTTTTTGACG[G/T]AGTCTCACTCTTGTC	54778
rs551320786	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59037704	AGCCGAGCGTGGTGG[C/T]GCATGCCTGTAATCC	54778
rs551340655	snp	G/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59062865	AGATAGTTCTTACAG[G/T]GGGAGGTGGGGAAAG	54778
rs551342540	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59093261	AGAGGCTTTGGAGGT[A/C]CTAGAAAGTTATAAT	54778
rs551372115	snp	G/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59061255	GGGCCTCTCTTAAGG[G/T]CAATTTCCTTCCAGG	54778
rs551405652	snp	A/C	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59091214	ATAAATGTAATATAT[A/C]CCTTTTTTGAATTTG	54778
rs551429839	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990301	TGTCGTAATTGAATC[C/T]CCAGAAAGAAATGCT	54778
rs551453839	snp	A/C	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59035756	AAGAGTGGCCCATTT[A/C]CTCCAGTTCCCAAGA	54778
rs551516378	snp	C/G			utr-variant-3-prime	RNF111	GRCh38.p7	15:59095510	TCACATCACCAGAGT[C/G]ATCAGTATAAATTTT	54778
rs551520783	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59067277	TCCCATTCTTCCTTC[C/G]TTTCCTCTCTTCCCC	54778
rs551548506	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59080832	TAAAGTATTCATAAA[A/C]ATAAAATACTAATAT	54778
rs551582204	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:58990985	ATGAGGAGTGAATTA[A/C]AAATATTTAAAGACA	54778
rs551589583	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59067432	ACTTGCGTTAAAACC[A/T]ACCCACCTTTCTTTT	54778
rs551591396	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58993944	TGAATCAATGTTGTA[A/G]TCATTTCCCTTATTC	54778
rs551600253	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59065267	TTAAAAATCTCTTTT[A/G]TATAGTTTCCATATA	54778
rs551639025	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59088179	GAGAGAGAGGCTTGG[C/T]GGGAAGTAGTGAAGT	54778
rs551687245	snp	C/G/T			downstream-variant-500B	RNF111	GRCh38.p7	15:59097753	TCATGGGTAGCGGGT[C/G/T]CCTGTAGTCCCAGCT	54778
rs551697711	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59043181	TTTTTTTGAGACAGG[G/T]TCTCATTTTGTTGCC	54778
rs551707468	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59050042	ACCACGCCCGGCCCA[C/T]AGTAGCCATTTTCTT	54778
rs551722221	snp	A/T			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020693	GAAACCTATTAGTTG[A/T]GAGAGGTTTAACTTA	54778
rs551752672	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58988416	TGAAGGTAACCCGGA[C/T]CCGGGGAGTTGGAGG	54778
rs551771857	snp	A/T			utr-variant-3-prime	RNF111	GRCh38.p7	15:59095055	ATGCTAGACCTACAG[A/T]TTATGTATACAGTTG	54778
rs551795244	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59065865	AAAATACAAAAATTA[A/G]CCAGGCGTGGTGGTG	54778
rs551797577	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58994033	TTTGTTGTTACTTAA[A/G]TTTTTTTTTTTTTTT	54778
rs551803407	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59091157	TAAATACAAAAAGGT[A/C]AGAATTTATTCTATG	54778
rs551804710	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59090409	TAATTTTTGTATTTT[C/T]AGTAGAGATAGTGTT	54778
rs551839923	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59061343	TTTTGAATATTTCCA[A/G]CCCTCACATTCAAGC	54778
rs551845454	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59019223	GGATTACAGGTGTGA[G/T]CCATTTATTTATTTT	54778
rs551851855	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59048280	TCAGCAATAAAAAAA[C/G]TATGAATATTGATAC	54778
rs551858937	snp	C/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59049434	TAGGTTCCAGCAGTT[C/G]AGGCTCCTGTCCATT	54778
rs551861871	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59057018	TCTCATTGGAAAGCT[G/T]CTCTCTTATTAAAAA	54778
rs551862118	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59047582	TGTTTTTTTTAATTA[C/T]TATTATGTTTTGAGA	54778
rs551863972	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59054188	GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC	54778
rs551928080	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59054183	ACCTTGTGATCCACC[C/T]GCCTCGGCCTCCCAA	54778
rs551974541	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59024900	TGACTACTCTGGGTA[A/G]TTCATATAAGTGGAA	54778
rs552022486	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58994437	CAGATTCACCAATTT[C/T]TAATGTTGTCACTCT	54778
rs552031021	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59077143	AGCATTGACCAATGG[C/G]CCAATTCTTTGTATG	54778
rs552046770	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59011601	CCCTCTTCTTGGTTT[A/G]TAAATGATCGCTTGC	54778
rs552097021	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59030229	GTAGTTGTGTCTACT[A/G]TCAGGAGAATTCAGA	54778
rs552132265	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59017685	TTGACAGATTTATTA[C/T]TTGAATTATCAAGAA	54778
rs552139530	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59060307	TATATTTTAATTCTT[-/A]AAAAAAAAAAAAATC	54778
rs552159554	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59028523	GTGGTCTCTCTCTCA[C/T]AGTGTGAGTAACTGA	54778
rs552173419	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59059656	CAAAAATTTATTCTG[A/G]AGCTTTCTTTAGTTT	54778
rs552189380	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59001903	TATACATTGGGCAGA[A/G]TAAGACATTAATAGC	54778
rs552236549	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59065554	TGCTGAAAGAAAGGT[A/C]CCAGATTAGAACCCA	54778
rs552268896	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59091499	CAGATTGCCTTTCAT[A/G]CCAATTAGCTCCCAC	54778
rs552274233	snp	G/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59012171	TTACAGGCATGCATC[G/T]CCACACCCGGCTGAT	54778
rs552279600	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59028153	CCATCATAGTTGAAT[C/G]CTCCGATGATCCCCA	54778
rs552307467	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59018076	TTTGTTGAGCTCTTA[C/T]AGACTACTTTCCATT	54778
rs552386191	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59010405	TTTATTTATTTATTT[A/T]TTCTTTCTTTTTTTG	54778
rs552399962	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58998908	TTTCAGATGACCATG[A/G]TGTTACAAAGTCATG	54778
rs552435689	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59015969	GATCCTCCCACCTCA[A/G]CCTCCTGAGTAGCTG	54778
rs552494471	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59083576	GCTAAATACACGTTT[C/T]CTAGGTGTGTTAACT	54778
rs552513597	snp	A/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59009412	TCCATTGTGCTTTTT[A/T]CAAGTGACCAAATGG	54778
rs552546904	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58987745	GCTGTAGGGGAGCAG[C/G]GGCAGTGGCGGCGAC	54778
rs552549354	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59035411	TGAGACAAGGCAAGT[A/C]CCTTCTGCATATGAG	54778
rs552569981	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59026260	GATGTGAATTACTAA[A/G]TCCCAACCCTAATTT	54778
rs552591377	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096675	ATACCTTATGATTAA[A/G]CCGAGGTTATAGAAG	54778
rs552600979	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59048496	TGCGAGCTCTTTTGG[C/G]GTTATTGGAAATGTT	54778
rs552603579	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF111	GRCh38.p7	15:59095886	TCTGTGCATTCATAG[A/G]ACTTATAAAGGTCCC	54778
rs552617853	snp	A/G/T			intron-variant	RNF111	GRCh38.p7	15:59046152	TCTTTCATTATCTCC[A/G/T]TTATTTACCAGTGTC	54778
rs552627317	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59078071	GAATTGGATAGATTC[A/G]AGTTGACCTCCCAGC	54778
rs552627699	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59071420	GTGCATAGTGGCTTA[C/T]GCCTGAAATCCTAGC	54778
rs552672146	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59088724	AAACCTCTGTTCACA[A/G]CTAATCAGTGTATAA	54778
rs552776157	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59015008	CCTGCCTTGGCCTCC[A/G]TAAGTGCTGGGATAA	54778
rs552852101	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59063197	TATAGAAAGTGCTTA[C/T]TGAGCCACCTACATT	54778
rs552897190	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59053310	ATTCATCTTATACTT[C/T]AGATGATTATAAGTA	54778
rs552897282	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59046382	ATTTTTTGTGGAAAT[A/G]AGGTTTCACCATGTT	54778
rs552903745	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59045228	AGTTTTTGTTCTTGT[A/C]ACCCAGGCCTGGAGT	54778
rs552931356	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59036736	AAATGTTTTACATTT[C/T]AAGTATTTTGTAATA	54778
rs552945526	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990163	GTTTATTGTTAACCC[C/T]CCTTGGGCTTCAGGT	54778
rs552975043	snp	C/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59052159	TGTTTTTTGTTCCTT[C/G]TGTATTTTTTTAAAA	54778
rs553057575	snp	A/G	0.0023933	0.0345097	utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58987687	CTCTCCTCGGTAGGG[A/G]AGGAATTGGTTAGGC	54778
rs553088977	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58996320	GCTCATACCTATAAT[C/T]CCAGCACTTCGGGAG	54778
rs553102408	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59014505	ATCTATGTGTTGACT[C/T]TTCTGCTGTGGAATT	54778
rs553156499	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59087097	TCTCTATGAAAGTTG[A/G]ATGTCCAATAGGAAG	54778
rs553185106	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59044116	GCTCACTGCAACCCC[C/T]ACCTCCCGGGTTCAA	54778
rs553201511	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59076336	TACTTGGCTTAAGAG[-/T]AGGGTATATTTTTTC	54778
rs553229739	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59056103	TAGTTTGAGGTTAGC[G/T]CAAACTAGTTTAGTT	54778
rs553235420	snp	C/T	0.00517822	0.0506191	intron-variant	RNF111	GRCh38.p7	15:59049749	TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT	54778
rs553269693	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59068589	CCAGCCTGGGCAACA[C/G]AGCAAGACTCCGAAG	54778
rs553344513	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59092994	GCAATAGAGTGAGAC[A/C]CTGTCTCTGAAAAAA	54778
rs553377605	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59019357	ATTTGAAAAAATACA[G/T]TGTTTTTAAAGGCCT	54778
rs553405016	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59007085	TACAGTTTTTAAAGT[-/A]AACTTTACATACGGT	54778
rs553425282	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59037800	GAGATCACGCCATTG[A/C]ACTCCAGCCTGGGCA	54778
rs553430649	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59061621	TACCTGTCCTCCTCT[A/G]CTAATTCCTAGTCTC	54778
rs553479334	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59060117	GGCTCAGGTGATCCT[C/T]CTACCTCAGTCTCTC	54778
rs553518425	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59058569	TGTAAAAAAGTGGGG[C/G]AGGGGAGACTTTTTG	54778
rs553561158	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59007704	TTAGTTTTAGTCTTA[C/T]TGGGTGTGTAATGGT	54778
rs553570497	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59093567	TAAACTAGTAGGACT[A/G]TTCCCTTCTTGCACC	54778
rs553580901	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59036356	TTGAGCCACCGCACC[C/T]GGCCAAGACTGGTAA	54778
rs553594155	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58994666	TATTTTAGTTAGAGA[C/T]GAGGTTTCACCCTCT	54778
rs553615141	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59042880	CAAGTGAACTTTATA[A/G]TCAGTTTGTTTACAT	54778
rs553620759	snp	A/T	1.6646e-05	0.00288491	missense	RNF111	GRCh38.p7	15:59066777	AGATGACTCAAGGAG[A/T]ACTACATCTAGTGCT	54778
rs553652261	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59007139	CCATTTAAGTTTTGC[C/T]AAATGCATCTATTTA	54778
rs553652287	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59013843	GCCCAGGCTGGAGTA[C/T]AGTGGTGCTTTCTTG	54778
rs553671594	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59006535	ATTGCAAACAGAAAA[G/T]ATGAAAGAATTGTAC	54778
rs553684768	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59013318	TGTCATGACTAAGAG[A/G]CCCACATTGATACAT	54778
rs553698625	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59018929	TTTGTTTCTTTTCTT[C/T]TTTCTTTTTTTTGAG	54778
rs553706467	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59005828	GCTATCATATGCATA[C/T]GTTACTTTGTTTAAT	54778
rs553708340	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59012273	GTCCACTTGCCTAGG[C/T]CTCCCAAAATGTTGA	54778
rs553737581	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59025128	ATGCTGTTACGATCC[A/G]CCCTCCTCCGCCTCC	54778
rs553753730	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59067403	GCTGGAAAACCCAGC[A/C]TGAGGGAGTAACTAC	54778
rs553787491	snp	C/T	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59041733	TGGTGATTGTAACCA[C/T]TCTGAATGCTCACCG	54778
rs553794299	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59011902	GAAGATAATGTCTTA[C/T]GGTTCACTACCAAAC	54778
rs553803946	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59092734	CATGATGGCTCACAC[A/G]TGTAATTCCAGCACT	54778
rs553811375	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59075836	ACTAAGAATCTTCCT[C/G]GTTTCAAACTAATTT	54778
rs553846837	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59047832	TGCCTGCCTCGGTCT[C/T]CCAAAGTGCTGGGAT	54778
rs553913906	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59046988	TCCTACCACCTCAGC[C/T]TCCGGAGTAGCTTTT	54778
rs553965112	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59000384	TCCAGGCTGATCTCA[A/G]ACTGCTAGGCACCCG	54778
rs553976275	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	RNF111	GRCh38.p7	15:58987505	GACACCTTTCAGTTC[A/G]CCAACAGACTGATAA	54778
rs553979259	snp	G/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59091607	TTATTTTGACGGACA[G/T]TTTATTGATGTATGT	54778
rs554021078	snp	C/T			utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096270	ATTTGTTTAAATATG[C/T]TTAATATGCCCCAGA	54778
rs554025292	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59042196	GCATATTGCTGCCTC[A/G/T]GCTCATTGCAACCTC	54778
rs554083354	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59023018	TTGGGAGGCCGAGGC[A/C/G]GGAGGATCACCTGAG	54778
rs554155327	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59076978	TTTTTTCTTCTACTC[C/T]AGTCATTTAAAAAAA	54778
rs554195664	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59071497	AGACCACCCTGTGCA[A/G]CATGGTGAAACCCCG	54778
rs554205219	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58994319	GCTGGGATTACAGGC[A/G]TGAGCCACCACGCCT	54778
rs554225474	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59017880	CTCCTGCTTCAGCCT[C/T]CCGAGTAGCTGGGAT	54778
rs554252615	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58994805	TTAAAAGTAAATTGC[C/T]TACATTATGCCCATT	54778
rs554263433	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59008902	GAAACTTAAAACAGT[A/G]TACTTTCATTTGTTC	54778
rs554292781	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59088973	AAAACTGTGAAAAAC[A/G]TGGCACTAAACAGTC	54778
rs554300238	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58998455	CCTCATTGTGTCCGT[A/G]TGTTCTTGGGAAGGT	54778
rs554310746	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59052931	TGTTTTTTAATGATA[C/T]GGAGAATTGATCTGC	54778
rs554346687	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59059821	GCTAACTGCTTACCA[A/G]TAGGGACACTGTAGA	54778
rs554359257	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59040102	CCAATGCTTTTGGCT[G/T]TTTTGAATTTAACCT	54778
rs554360826	snp	G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59059495	ATTGGATGCACTAAG[G/T]CTACTCCTTAGTTAT	54778
rs554387995	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59003978	TTTCCTGATTGACTT[C/T]TCTTGGTTTTGTTCT	54778
rs554392481	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59052130	AAAACAGTGATTACC[A/T]TTTTTACTGTGTGTG	54778
rs554395938	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59076473	GGCACAGTAAAGTAA[A/G]TTTTTAAGAATTCTC	54778
rs554443088	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59089443	AAGTTTGAGCTACTA[A/C]GAGCCTCAGGCTTAA	54778
rs554455811	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59055111	GCATAAACTAGCTCA[C/T]GCAAGTAATATTTCT	54778
rs554458430	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59039491	TATCATTATGAATGC[A/G]TGAATTTTAGTATAT	54778
rs554484721	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59058168	TAAAATGCAGTAATA[C/T]TTTGGTAACACGTCT	54778
rs554503879	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59028930	GATTACAGTCAGTGC[A/G]CCACTATCCTGGCTA	54778
rs554505286	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58999056	GTAAAGTTTTGGGGT[A/G]GTATCAAAGAGGAAT	54778
rs554514685	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59077736	TGATTGCTATGTCAG[A/G]GGGCTAAACTTTCAG	54778
rs554577047	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59040915	ATGTAAAACATTTAC[C/G]TAGCTTCAGAGTCAA	54778
rs554582926	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59005871	CCTTTGTGGTAAATA[C/T]TTTCATTTTTCAGAT	54778
rs554612002	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59090066	GTGGGGAACGGAATG[C/T]TTTTGACTCAGCTAA	54778
rs554626463	snp	C/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59034411	CCTCGATGCTAATGT[C/T]GTGATGATAATAAAA	54778
rs554638372	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59046994	CACCTCAGCCTCCGG[A/G]GTAGCTTTTGTTGAG	54778
rs554638803	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021603	GTACTCTCATTTAAC[C/T]GTTACGGAATTTTAT	54778
rs554642043	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59033748	CTTAATTCATTTAAA[A/G]ATCTTATTTAATACT	54778
rs554658224	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59039512	TTTAGTATATTTGAT[A/G]GGTTTCAGTTTGTTG	54778
rs554745386	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59000365	GACGGGTTTCACCAT[A/G]TTGTCCAGGCTGATC	54778
rs554768819	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59039131	CACCATACCTGGCTA[A/T]TTTTTTATTTTTAGT	54778
rs554830246	snp	C/G	0.00633158	0.055908	intron-variant	RNF111	GRCh38.p7	15:59052271	ATTAGCTGACAGGAA[C/G]ATGCCTTTAAATGTT	54778
rs554849829	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59009498	ATCTGAAATTATCAA[A/G]TTCTAAAGAAAAAGT	54778
rs554906410	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59002616	AGTCATTTAGATCCA[A/G]GCTTTGCTATCAGGT	54778
rs554907327	snp	G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59014936	TTTTGTATTTTTTTA[G/T]AGACAGAGTTTCACC	54778
rs554916022	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59075732	AAAAATTGGTTTAAC[C/T]GTAAAACCACTACAG	54778
rs554937514	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59087939	TGGTGAGTGATGTAG[A/T]TGGGGCACCTCTTAG	54778
rs554943260	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59008755	AGGGTTTTTAAAAAT[C/G]ATATTACATTTATCA	54778
rs554953864	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59045130	ATGTTACATAAGCCA[C/T]GTAAAAGGTGTTCGA	54778
rs554965765	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59051437	CACTCCAGACTGGGC[A/G]ATTGAGCGAGACTCT	54778
rs555032287	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:58991260	TGAGATCTGCACTCC[A/G]GCCTGGGTGACAGAG	54778
rs555033924	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59020048	TTTGAGTTTAGTTCT[C/T]TTAGATTTTATTTTA	54778
rs555072812	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59069446	AGAATATTTTGTTAT[C/T]AATAAAATAATACAG	54778
rs555116519	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59019646	CATTGTACTTTTAAA[C/T]ATGTTATTATTGGAT	54778
rs555128401	snp	C/T	0.0014002	0.0264223	synonymous-codon	RNF111	GRCh38.p7	15:59076166	GCCCCAGCCCCAGCC[C/T]CCTCCACAGCCCTCT	54778
rs555140323	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59000578	AGCCAGGTATGGTGG[C/T]GGGCGCCTATAATCC	54778
rs555140705	snp	A/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59093192	ACAAGGTTTGGCCAG[A/G]GAAATTTCGTAGTCA	54778
rs555151736	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59066208	AAAACATGATCTATT[G/T]CCATACTTACACATC	54778
rs555202089	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59081910	TACTCCTGTGGTCCC[A/G]GCTACTGGGTAGGCT	54778
rs555223216	snp	A/G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59068479	GGTGTGATGGTGTGT[A/G/T]CCTGTAGTCCCAGCT	54778
rs555223849	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59002157	TAGGTAACTGAAACC[A/G]TAGACAGTAAATTGT	54778
rs555227187	snp	C/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59059374	CAGCGTTGGCAAGGA[C/T]GTAGAGAAATTGGAA	54778
rs555284729	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59032403	ACAGTTCTAGTCACT[A/G]AAAAAGACTGGTTAA	54778
rs555286931	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59074452	GCTTCTACATCAGCA[C/T]TTGCTGCTTCTCCTT	54778
rs555296788	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58994877	ATTGTATTCTTTTGC[A/G]TTATCACTGCACCAG	54778
rs555309632	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59008340	CTCCTGCCTCAGCCT[C/T]CTGAGTAGCTGAGAC	54778
rs555352142	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59086374	TCTGCCCACCTTGGC[A/C]TCCCAAAGTGCTGGG	54778
rs555365322	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59057239	CAGCGAACAAAAAAT[C/T]GTCTAGCCCAAAATG	54778
rs555424149	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59091899	TACAATAGGGTTCAC[A/G]CTTCTATGAGAATCT	54778
rs555620885	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59061129	TTACGTACATTTTAT[A/G]TGATACAGTCCCAAC	54778
rs555634451	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59032000	CTGGAGTGCAGTGGC[A/G]CAATCTCGGCTCACT	54778
rs555679561	snp	C/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59026362	ATTCTACACTAGTAT[C/G]AGGAGTAATTAGCAT	54778
rs555683054	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59067360	TTTCTCCTTTCCCTT[C/T]CCCTTCCCCTTCTTC	54778
rs555695062	snp	A/C/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59066624	CAAAAAAAAAAGAAC[A/C/G]TGGCACTATCACATT	54778
rs555699971	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59023135	TGTCTGTAATCCCAG[A/C]TACTCGGGAGGCTGA	54778
rs555713774	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59037750	CTGAGGCAGGAGAAT[A/G]GCTTGAACCTGGGAA	54778
rs555758380	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59066183	AATAAATCATTTACT[G/T]TGCCATAGGAAAACA	54778
rs555768192	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59082355	GTAAAAATCAGTGTT[A/C]AAATTGATGATTCTG	54778
rs555772343	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59024959	CTTATTTCACTTAGC[A/G]TAATGTCTTCAAGAT	54778
rs555775682	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59000916	AAACGAAATCTGCTC[C/T]GGTGGGGAAACAAAG	54778
rs555822562	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59043345	TTATTTGGTAGAGAC[A/G]GGGTTTTCACCATGT	54778
rs555824424	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59037399	GAAGCTAGGTTTGAG[A/T]ATAGGTGTTAATTTT	54778
rs555840127	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59036350	ACAGGTTTGAGCCAC[C/T]GCACCCGGCCAAGAC	54778
rs555852242	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59042135	GCCAAATTTTTTTTT[C/G]TTTTTTTGAGACAGG	54778
rs555871466	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59038715	TTAATTCTTTTTTAT[A/G]TATGGCATCATTTCT	54778
rs555885755	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59042815	AAGAACACTCTTTTA[A/G]TTATAAAATCTTTAA	54778
rs555895628	snp	C/T			utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096643	ATGTGTGCAGATGGA[C/T]GATGGATTTAAAGAG	54778
rs555904193	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59036893	GGAGTGCAGTGGTGC[A/G]ATTATGACTCGCTGC	54778
rs555920859	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:58988084	GTGAGGGGAACGGGG[G/T]GGGAGGGGATCCATT	54778
rs555961301	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59013270	TCGCTCACTCAGTTA[C/G]CCTTGTTGTTAACAT	54778
rs555965133	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59041648	TTTGGAATAGTATTC[A/T]AGAAGGCAGTTGTTG	54778
rs555971583	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59025319	TTATTAGGTTGTGTA[C/G]TCCTAGCAGAAATCT	54778
rs555994609	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59051208	CCTGTAATCCCAGCA[C/T]TTTGGGAGGCTGAGG	54778
rs556028041	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59041119	GAAAGTATATATCTC[C/T]GTATATCTCATTTCT	54778
rs556046310	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59080606	AAGAGTGAGTGCAGG[A/C]GTGAGCATATACACA	54778
rs556050910	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59024358	AGTATGTGCGAGTCA[A/G]CTGTTTTCATTGCTA	54778
rs556076288	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59078483	GAGTTCAAGGTTGTA[A/G]TGTGCTGTTATCACA	54778
rs556101396	snp	G/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59017807	TTGTTGTCCAGGCTA[G/T]AGTGCAATGGCACAA	54778
rs556108364	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59036825	TTCATTTGTGGTTCT[C/T]TTTGGTTTGGTTTTA	54778
rs556134540	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59069939	TAGTCATGTAGATAG[C/T]CCTCACTGCTTGCTT	54778
rs556136659	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59030388	TAATAACCACTTAAA[A/T]ATGTCATACCAGGAG	54778
rs556140723	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59072891	TTATTAAAAAAAAAA[A/C]AACAAAACACTTCCA	54778
rs556160033	snp	C/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59088726	ACCTCTGTTCACAAC[C/T]AATCAGTGTATAACC	54778
rs556164246	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59005022	CAAGCATAATCTCCT[A/G]CATGGTTTAAATTAT	54778
rs556170618	snp	C/T			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022000	GAGTAGCTGGAACTA[C/T]AGGCGCGTGCCACCA	54778
rs556264691	snp	C/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022464	ACTTCCAGATTCTGA[C/G]AGTTCTAATCTCCAT	54778
rs556302140	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59024693	GTCGTTTAAATGTAC[A/G]TAACATAAAATTACC	54778
rs556308273	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59000353	ATTTTTAGTAGAGAC[A/G]GGTTTCACCATGTTG	54778
rs556319412	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58994570	GTAACCTCCATCTCC[C/T]AGGTTCAAGCGATTC	54778
rs556366015	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59005689	AAAAAAAATGTATGT[A/G]TATGTATATGTGGTG	54778
rs556402020	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59084623	TTCTTTGTGGTGAGT[A/G]TATTTAAAATCTTTT	54778
rs556404739	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59011811	TACTGGGTGTTAGGA[C/T]TTCAACGTATGAATT	54778
rs556412806	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59047692	GCTGTCTTCCTACCT[C/T]AGCCTCCCAAGTATC	54778
rs556425382	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59053997	CTGGAGGGCAGTGGC[A/G]CCATCTTGGCTCACC	54778
rs556438645	snp	G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58999201	TGGAATACAGATGCA[G/T]ATGTGACAATCCAGT	54778
rs556446245	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59044286	TCCATCTGCCTTGGC[C/G]TCCCAAAGTGCTGGG	54778
rs556454454	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58998440	AGTGAGTGTTCTTCC[C/T]CTCATTGTGTCCGTA	54778
rs556464356	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59080317	GTGGAGACGGGGCTT[C/T]GCCATGTTGGCCAGG	54778
rs556469435	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59090868	TTTGAGACCAGCCTG[A/G]GCAACATATAAACTG	54778
rs556475141	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58994285	CTCAAGTAATCCTCC[C/T]GCCTTGGCCTCCCAA	54778
rs556478111	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF111	GRCh38.p7	15:58986805	CAGGCGTGAGCCACC[A/G]TGCCCGGCCAAAATC	54778
rs556494036	snp	A/G	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59028061	CGAACTCCTGACCTC[A/G]GGTGATCTGCCCGCC	54778
rs556548225	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59089335	AACTTATCTTGAAGT[C/T]GAATTTTGTTGGAAA	54778
rs556563144	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:58991010	AAGACAAATACTTAG[A/C]TGAGGCTGGGTGCGC	54778
rs556567948	in-del	-/G	0.0123036	0.0774623	intron-variant	RNF111	GRCh38.p7	15:59072822	ACCACTTTTGCTGCA[-/G]GTTTTTTGTTTGTTT	54778
rs556573206	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59011300	CTATCATAACACTTA[C/T]ACTGCATTTTGATTA	54778
rs556577206	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59003521	CTCCCACCTCAGCCT[C/T]TCCAGTAGCTGGGAC	54778
rs556583617	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59090326	CCTGCGCCTCCTGGG[C/T]TCAAGCAATTCTCCT	54778
rs556606924	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59076795	CTATGTAACATATTT[A/G]CTATTTTGTTAGATC	54778
rs556672921	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59059390	GTAGAGAAATTGGAA[C/T]CCTTGCGAATTGCTG	54778
rs556736643	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59065142	GTTCCAGAATTCTAA[A/G]GATTCTGAGGAGATG	54778
rs556748808	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59064671	CAAGTTCACAGACGC[A/G]TGAATTCTAGTTCCC	54778
rs556757237	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59009450	TTAATATCAAAGTCA[G/T]TATGACTTAATATCA	54778
rs556759903	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59063978	GTATAACACTTTTAC[A/G]TAGAGACTAAGATAA	54778
rs556762597	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59067969	ATTAGTTGGTATTAT[C/T]ATTGAGTTCGCAAAA	54778
rs556816763	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59027076	TGTGAATTGCTTCTT[G/T]GTAAATTAATGTATG	54778
rs556826961	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59052186	AAAAAACCTTTTTGA[C/T]AGATAAGATTTTTAT	54778
rs556890907	snp	G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59069266	AGGGAGCATCAAGAA[G/T]AATTTTCCAGTGGAT	54778
rs556902884	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59006393	CTCAGGCAACTACTC[A/G]TCTGATTTTTGACAT	54778
rs556918853	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59057773	TGCTAAGTGATTACT[C/T]TCTGTAAGGCATCAT	54778
rs556952370	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59068677	GGCATTAAGCCACCG[G/T]GCCCGGCCAAGCTAC	54778
rs556971313	snp	A/C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59039654	TCTCTGGTATATCAA[A/C/G]TTGGTGCAGATTAAT	54778
rs556994111	snp	C/T	0.00835141	0.0640778	intron-variant	RNF111	GRCh38.p7	15:59039863	CTGGGACTACAGGCA[C/T]ATGCCACCGTGCCCA	54778
rs557051419	in-del	-/TTTTTTTT			intron-variant	RNF111	GRCh38.p7	15:59017767	TCTTTTTTTTTTTTT[-/TTTTTTTT]GAGATGGAGTTTCGC	54778
rs557080150	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59051721	AGGTTGCAGTAAGCC[A/G]AGATCATCCCACTGC	54778
rs557082265	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59008949	GTTAATATTGTCACG[C/T]ATTTTATTTTATTTT	54778
rs557090225	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59084791	CCCACCCTCTCCCCA[G/T]CCTCTGGTAAACAAC	54778
rs557092216	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59033075	TCTGAACTGAGGGAA[A/G]AGATTAATTTCTTGT	54778
rs557094448	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59075581	GAGTCCTAAAGTACT[A/G]GTCACAATGTTGGGA	54778
rs557119298	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59015124	AGTTTTAGATCAGTA[C/T]TTACTAGGACCAAAG	54778
rs557161275	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59015848	ATAGCATGTTTATAA[C/T]GTATTCTGGTTATTT	54778
rs557199026	snp	G/T	0.00517822	0.0506191	intron-variant	RNF111	GRCh38.p7	15:59057491	AAGAGACCCCCCTTC[G/T]TTTCAGATTTAATTG	54778
rs557209542	snp	A/G	0.0119091	0.0762411	intron-variant	RNF111	GRCh38.p7	15:58992255	TCACCATGTTAGCCA[A/G]GCTGGTCTTGAACTC	54778
rs557219662	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59050887	ATGTATTTCTTTTGC[A/G]TAACTGAAAATTAGA	54778
rs557219693	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59043533	CCATTAGTCATGAAG[A/G]TGAGATACGACATCT	54778
rs557279029	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59050274	TGATGTCTACAACAT[C/T]GCTTTTTCTTGTAGA	54778
rs557279156	in-del	-/TCA	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59019063	CGTGTAGGTGAGACT[-/TCA]GGCACGTGCCACCAC	54778
rs557281772	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021109	TTGTATCATTCTTAT[A/G]CCTCTGTGTCCTCAT	54778
rs557311305	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59008279	CTGCAGTGCAGTGGC[A/G]CAGTCGTGGATCACT	54778
rs557318775	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59026916	TACACCAAACCACCC[C/T]CCCTTGCTCTCCTCT	54778
rs557336602	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59019460	CCAATTTGGAGTCCT[C/T]GTTCATCCAGAAATG	54778
rs557350182	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59014255	GGCACTACCAGATGC[G/T]ACAGGCTTGTATTTT	54778
rs557405971	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59026389	GCATGCAGTCATCAT[A/G]ACATAGCAATGAAAT	54778
rs557417238	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59056687	GAGTATCAGTACCCA[A/G]TTGTTTATGAAGAGA	54778
rs557438204	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59038492	GCATTGATTGAGTTA[A/T]AGTTTTTGGTTTTAT	54778
rs557439659	snp	A/C	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59041573	CTCAAAAGAAAAAAA[A/C]AATTACTGCAATAAA	54778
rs557503894	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58996394	CCTGGCCAACCTGAT[A/G]AAACCCTGTCTCAAC	54778
rs557549248	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59044543	TGTACTACTCATATT[C/G]TTTCTGGCCTGGTAG	54778
rs557583254	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:58996583	AGACTCCATCTCAAG[-/A]AAAAAAAAAATTAAA	54778
rs557602439	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59061254	TGGGCCTCTCTTAAG[A/G]TCAATTTCCTTCCAG	54778
rs557628243	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59001607	GCTCTCCACATTTGG[C/T]GAATAGGTTCACTTT	54778
rs557656845	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59094320	GGAAAGTGTAGTTAC[C/T]ATATATTTGCCACAT	54778
rs557658730	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59086562	TTGTTATATAAATGG[C/T]ACAGAAAAGGGAATA	54778
rs557681865	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59000458	GGCTCACATCTGTAA[C/T]TGCAGCACTTTGGGA	54778
rs557690109	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59006974	TGTATTTTTAGTAGA[A/G]ATGGGGTTTCACCAT	54778
rs557703339	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59013898	GGTTCAAGTAATTCT[C/T]ATGCCTCAGCGTCCC	54778
rs557773646	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59092883	TGTGCACCTGCAGTG[C/T]CAGCTACTCAGGAGA	54778
rs557776889	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59036549	AGACTTGTTCACTAC[C/T]GTGAGAACATGGTAT	54778
rs557800249	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59091904	TAGGGTTCACGCTTC[C/T]ATGAGAATCTATCGC	54778
rs557843843	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59055298	CTATCCTGAGCTAAA[C/G]ATACAAGACCTTGTG	54778
rs557865413	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59070570	GCATTGAAGACATAC[A/T]TTGTATTTGCCAACT	54778
rs557873171	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59085212	ATTTTGTTTGCCCTT[C/G]TTTTATAAGGTGTAG	54778
rs557904020	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59068608	AGACTCCGAAGTTCG[-/T]TTTTTTTTTCTTTTT	54778
rs557907187	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59038943	ATGGTCTTGCCCAGA[C/T]TCATTATATTAGGGG	54778
rs557920548	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59067971	TAGTTGGTATTATTA[C/T]TGAGTTCGCAAAATG	54778
rs557932069	snp	C/T	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:58989465	TAAATCTAAATAATA[C/T]TTTAGGAAAAAGTAG	54778
rs557948475	snp	A/G	1.64765e-05	0.00287019	missense	RNF111	GRCh38.p7	15:59031279	GGAGATTCTGATACT[A/G]TGACTTCAGATGAGG	54778
rs557949994	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59066524	CTGAGGGAGGAAAAT[C/T]GCTTGAACCCAGGAG	54778
rs557968890	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58994701	CAGGCTGGTCTCAAA[C/T]CCATGACTTTAAGTG	54778
rs557977761	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59073908	TTCATAGTCTGCAGA[C/G]TGGATGTTGTGTTAG	54778
rs557979747	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59067461	TTTTAATTGTGGTGG[C/G]TTTGGGAAGAGGAAA	54778
rs558012796	in-del	-/TATTT	0.00953873	0.0683987	intron-variant	RNF111	GRCh38.p7	15:58992037	CTTGCAAATGTCTGG[-/TATTT]TATTTTATTTTATTT	54778
rs558028915	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59037231	TAGGGATTTCTATTA[A/T]GTGTAGAAAGCCAAA	54778
rs558042831	in-del	-/TG	1.65261e-05	0.0028745	intron-variant	RNF111	GRCh38.p7	15:59085639	TAAGGAGGATTAAAC[-/TG]TTCTCATCCTTTCGT	54778
rs558046247	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59085387	TTATCTTGGAAGGGA[A/G]CTTCGTAGCCATATA	54778
rs558074313	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59089903	TGCTTCTGGGAGTTA[C/T]AGAAATATTTGTAAG	54778
rs558092526	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59042651	TTTTTTCATGTGACT[A/G]TACAGTTGTCCCCAA	54778
rs558119560	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RNF111	GRCh38.p7	15:58987587	CGGGAATCGAGCAAG[C/G]GCAGAAACAAACAGA	54778
rs558138374	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59071685	GGGTAACAGAGATCC[C/T]GTCGCAAAAAAAAAA	54778
rs558167554	in-del	-/TG	0.0185938	0.0946107	intron-variant	RNF111	GRCh38.p7	15:58989054	CTTTCCCATTTTTGT[-/TG]TGTGTGTGTGTGTGA	54778
rs558208106	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59009784	ACATGGCAAAACCTC[A/G]TCTCTGCAAAAAATT	54778
rs558210517	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59012400	GTGCTTTGAAGTACT[A/G]CTTATCTGTTCTCAT	54778
rs558235295	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59041321	AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA	54778
rs558241519	in-del	-/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59083608	TATTACATGTGTTTT[-/G]GAAAAAAAATGCACA	54778
rs558283283	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59072732	GCTGGGATTACAGGC[C/G]TGAGCCACCACACCC	54778
rs558288281	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59060317	ATTCTTAAAAAAAAA[A/G]AAATCCTTGACATGG	54778
rs558288668	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59015217	AATAAAAATAAAATA[G/T]GATGGATAAGATAGA	54778
rs558301821	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59047110	TTACAGGCATGAGCC[A/G]TCATGCCTGGCCAGG	54778
rs558304469	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58992575	GTAATCATAGCACCT[C/T]GGGAGGCTGAGGAAG	54778
rs558339039	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59077957	TAAAAAACATTTCCC[A/G]TATGCTTTAGTTCAC	54778
rs558375137	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59029590	TGGGAGACCTGTAAG[A/G]TTATATATTTCTGTA	54778
rs558409477	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59022697	ATATAAATCATTCTT[C/T]CAATGTCTTTTAAAT	54778
rs558414025	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59046745	TAAAATTAGAGACTT[C/T]CGTGCTTCAAAAGAC	54778
rs558429940	snp	G/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58988017	TTCTGTCTTCCTTCC[G/T]GGGTCAGTGATTCCC	54778
rs558441967	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59044124	CAACCCCCACCTCCC[A/G]GGTTCAAGCGATTCT	54778
rs558442569	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59074539	CTATCTTCAGACTTT[C/T]CTTCTGCAGCCTCCT	54778
rs558453777	snp	A/C	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59084018	ATTTATTTTATGACT[A/C]ATCTATAGATGTTTA	54778
rs558480271	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59023778	AGTGTTTCACTATTA[A/T]CCATCAGTTTTTTTC	54778
rs558483578	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59080660	TTCTTTTTTATCAGT[C/G]GGGATTTTGTCAGTA	54778
rs558556433	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59000037	GGCCCCACCTCCAAC[A/G]ATGGGAATTACACTT	54778
rs558620205	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:58999622	ATTACAGGTGTCAGC[C/T]ACTGTGCCCGGCCTA	54778
rs558620700	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59028044	GTTGGCCAGGCTGGC[C/T]TCGAACTCCTGACCT	54778
rs558673191	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59009815	CAAAAAATTAGCTGG[A/G]CATGATGGCTCATGT	54778
rs558705093	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59064647	GTCAGTTTGTATTTT[C/G/T]CTTCCGTCCAAGTTC	54778
rs558744420	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59033822	ATTACGTTATTTTTA[A/G]CTACATTATTTTCAG	54778
rs558744870	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59004928	AGAGACACTTGGGAA[G/T]TGAGACCCAGTGGAG	54778
rs558791699	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59051802	AAATAAATAAATAAA[C/T]AAATGAATAAATAAA	54778
rs558838513	snp	C/T	0.000330633	0.0128533	intron-variant, utr-variant-5-prime	RNF111	GRCh38.p7	15:59004117	TTATTTATTTTATTC[C/T]AGTGTGAATGCATGT	54778
rs558846598	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59089560	TGAAGTCAAATTTTA[C/T]GAGCAGTTGAATTGA	54778
rs558857491	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59059205	AAATGAGAAAAGATT[G/T]GAATAGATATTTCTG	54778
rs558877365	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59010100	TTTATGCCCTCACAT[A/G]AAATCATGGCTAAAA	54778
rs558882447	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58991334	CAAATACTTAGCTGA[A/G]CTTACATTTTAAAGA	54778
rs558908487	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RNF111	GRCh38.p7	15:59097540	CTTTATTTTAGCTGC[C/T]AGCACACTTCAGCAT	54778
rs558921595	snp	C/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:58997772	AGTGAGCCAAGATTG[C/G]GCCACTGCACTCCAG	54778
rs558929205	snp	C/G			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020461	CAGATACTGTTCAGG[C/G]TTGTGAGGTTAGATA	54778
rs558957343	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59082414	TTGAATGTTACTAAC[A/G]AGAGGGAAGGAAAGT	54778
rs558970980	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59002240	CTTGACTATCTTCCC[A/G]CCATTTCTCTGATGT	54778
rs559008495	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59001736	GAACACCTACAAAAC[A/G]TACATTATCATGGGA	54778
rs559018708	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58991646	TCAGCCATAGTGACG[A/G]TTTGGAGGAAGACTG	54778
rs559040317	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59094674	TTTATAGAAGAGGAA[A/G]ATGCTTAGTACCTTC	54778
rs559041454	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59034336	TTCAGAGGGTATATG[C/T]ATTGAAAATGTTGTT	54778
rs559041625	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59064111	AGCCCTAAAAGACTT[C/T]TGATCATGGTCAGTT	54778
rs559044192	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59059621	TCATATCTAAGAAAC[C/G/T]GTTGCCTAATCCAGG	54778
rs559046438	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59082876	AGTAACCTTTTATAT[A/G]GAAAATTGCCAGTTT	54778
rs559060862	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RNF111	GRCh38.p7	15:58986617	CCACCCTGGCTCAAG[A/C]GATTCTCCTGCCTCA	54778
rs559097089	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RNF111	GRCh38.p7	15:58985690	TCCCAGCTTCAGAAC[C/T]ACTGATTTAACCCAA	54778
rs559130450	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59070829	GGGACTGTTGGGTGA[C/G]TTGAGCCTTTGACAA	54778
rs559139868	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59087536	TGTATGTTATAAGTA[C/T]GTGATAATGATAGTC	54778
rs559142867	in-del	-/T	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59039235	CCCAAAGTGCTGGGA[-/T]TTACAGGTGTGAGCC	54778
rs559148970	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59046598	AGATCATAGACCTAA[A/G]TGTAAGAACTAAATG	54778
rs559204408	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59076318	TCTTAAATTTTTAGT[A/G]TTTACTTGGCTTAAG	54778
rs559211163	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59039192	TGGTCTCGAACTCCT[A/G]ACCTCAGGTCATCTG	54778
rs559225874	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58997383	ATGTAACTGATGTGA[A/G]CACCAGTTGACATTT	54778
rs559291657	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59013963	CTGGCTAATTTTTGT[A/G]TTTTTTAGTGGAGAC	54778
rs559300215	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59045812	TTGTACTTCTACCTT[A/G]AGCTGCATTGTGTTT	54778
rs559337881	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59077808	TTACACACCTCATTA[A/G]GAGTGTGTTAATGAG	54778
rs559355848	snp	A/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:58989581	GGCCACTTGTTTGCT[A/G]GTTATTTCACCAGAC	54778
rs559357352	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59080823	TTTACTTGATAAAGT[A/G]TTCATAAAAATAAAA	54778
rs559374841	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59074981	GAGAGCAGGGTAATG[A/G]GGAAACATCTGGTCA	54778
rs559383707	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59034901	TGGGACAACTTTTTC[A/G]TACAATGTGCTTGTA	54778
rs559445048	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59043742	TTGCTTATACCTTCA[A/G]TAACTTTAATTGTGA	54778
rs559477098	snp	C/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59013024	GATTATAGGCGTGAG[C/G]CACCGCGACCGGCCT	54778
rs559482153	snp	C/T	0.00358779	0.0422022	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096521	TCAAATTGACATTTG[C/T]ATAATTTGACATTTA	54778
rs559504581	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59080017	TAATTCTGAGAACAC[A/G]TACAAGCGGTCAAGA	54778
rs559534217	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59051117	AAATAAGGATGCACT[C/T]TCCAAGTTTAGAATG	54778
rs559538254	snp	A/G	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:58999497	TGCACCATCACACCC[A/G]GCTAATTTTTGTATT	54778
rs559565023	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59079486	AACAAGGCATACTTT[A/G]AAAATATAGTTGAGT	54778
rs559606494	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59056432	ACATATGTGAATTTG[C/G]CCACATATTGGGAAT	54778
rs559632864	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59019164	GGGTGGTTTTGAACC[C/T]CTGGGCTCAAGTGAT	54778
rs559651890	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59001107	ACAGATGTAAAGGAA[A/G]TGAATGAGTGAGCCT	54778
rs559660139	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59042929	GGAGGTCTATGATGG[C/T]ATTTTTATTGGGATT	54778
rs559666347	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59049034	GGAGCCCAGGAGATT[C/G]ACGGCATGAGCGTGA	54778
rs559677011	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59054907	TCACCTTTCTAAAAG[A/G]TTTATTTTTTTATCC	54778
rs559697936	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59061311	TGTTCTCCACAACCC[A/G]TCCTTATCTTGTACC	54778
rs559704383	snp	A/C	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59067663	CTTAATCTAAAAATC[A/C]CTTTTTAAAAAGGCT	54778
rs559715272	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59055902	TGATAAAAGGAAATC[G/T]CTTAATATGCTAGAA	54778
rs559715359	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59025902	CGCCTGGCTAACTTT[C/G]CATTTTTGGTGGAGA	54778
rs559736637	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59055982	AGATTTTTTAATCTC[A/G]TTTTTAATTGATATC	54778
rs559746068	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59028239	TAAAGGGAATCTTAC[A/G]TTATGTTATCTTTTT	54778
rs559777322	in-del	-/A	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59009396	TAGAACCCACTTTAT[-/A]TCCATTGTGCTTTTT	54778
rs559854438	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59048260	TCCATATGATTGGAT[A/G]CTACTCAGCAATAAA	54778
rs559899221	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59018463	AAGTTGTGTTCTAAT[A/G]TAGTGAAAAATTTAA	54778
rs559915564	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59060603	GGGCACCACTACACT[A/C]CAGCCCAGATGACAG	54778
rs559977814	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59042382	TCCACCCGCTCGGCC[C/T]CACAAGGTGCTGGGA	54778
rs560074299	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59053388	CAACTAATAATCTAA[C/T]GGATGAATCTTAATT	54778
rs560076231	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59006646	TTTGTTCCTCCAACC[A/G]TCCATCAACCAAACC	54778
rs560122794	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58993277	ACTTTGGGAGGCCAA[A/G]GCGAGTGGATCACCT	54778
rs560145786	in-del	-/C	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59042809	TACAGGAAGAACACT[-/C]TTTTAATTATAAAAT	54778
rs560160739	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59012566	TTTATTTGGAAAATT[A/G]CCAGTGGTAATTTGA	54778
rs560228881	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59059974	GCAGATTAGAAAACT[A/G]CATGTGGCTGGATCA	54778
rs560232825	in-del	-/CA	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:58991402	GTCTCATGTTCTAGG[-/CA]CAGTCACTGGTCTTC	54778
rs560239894	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59045122	GTTTCAAAATGTTAC[A/G]TAAGCCATGTAAAAG	54778
rs560294138	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59066211	ACATGATCTATTGCC[A/G]TACTTACACATCACA	54778
rs560320330	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59016701	TTCTCCAAAGAGTTC[A/T]GTATAGCAGGGTTCC	54778
rs560349922	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59065302	TTAGTTTGAGGAAGC[A/G]TTTCTAGGTTTTAAA	54778
rs560364822	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59040516	TAAGTGAATATTTCC[A/G]CTGCAAGTTTAGGAT	54778
rs560380558	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:58988123	CGCGTGCGCGCAACG[G/T]GGGAGGGGCCGGCCT	54778
rs560399245	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59089860	GGACTGCTACAGTGG[C/T]TGGGAATCACATGTG	54778
rs560408556	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59016156	TTGGTTAAAAAATAT[A/G]TATATGTATATATAT	54778
rs560419006	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF111	GRCh38.p7	15:58986917	TTAATGTTTAGTGAA[C/T]ACTTAATTGGCAAGT	54778
rs560426104	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59046863	TATAAGGAACTCTTT[A/G]TTTTTTATTATTATT	54778
rs560455279	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58999349	GCAGTGGGGTTTGTT[G/T]GTTTTTGAGACGGAG	54778
rs560458946	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59078525	TCCTTGTACTCCTGC[C/T]TGGACAACATAGTGA	54778
rs560461900	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59068944	GTTGGGTCTGTGGCG[C/T]GTGCCTGTAATCCCA	54778
rs560462536	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59043029	ATGTCTTCATTTGTT[A/G]ATGTCTAGTTTTGTA	54778
rs560470949	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58992761	GGAGGCAGAGGTTGC[A/G]ATGAGCCGAGATTGT	54778
rs560504350	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58990597	GGAGGTTGCAGTAAG[C/T]GGAGATCGTGCCACT	54778
rs560530664	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59083552	AAAAAAAAAAAAAGT[A/G]TGAATCAAGCTAAAT	54778
rs560549999	snp	C/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59080789	AGGGAGCAAGTTGCT[C/T]GAGCAGTTGCTTGAA	54778
rs560574201	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59084315	TAAAACTATTGGAAG[A/G]GATGCCTTGTGATTG	54778
rs560610839	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59053691	CATAGTGCTTGGTAC[A/G]ACATTGACTCAATTT	54778
rs560612835	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59065051	ACCCAGAAGAGATTA[G/T]CTAGGTACTTTGAGC	54778
rs560614675	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59047328	TATGAGATCTCATTT[G/T]TATGAAAAATTTAAA	54778
rs560624283	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59076579	TAAAATATAACCATG[A/G]TTGGGCATGATGGCT	54778
rs560631187	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59013030	AGGCGTGAGCCACCG[C/T]GACCGGCCTGGTTCC	54778
rs560653747	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021972	TCAAGCGATCCTCCC[A/G]CCTCAGCCTCCCGAG	54778
rs560671017	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58991061	AGCACTTTGGGAAGC[C/T]GAGGCGGGTAGATCA	54778
rs560676511	snp	A/G			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986881	TATTGAAAAAGATGA[A/G]TTGATGGCAAAGGGA	54778
rs560732717	in-del	-/GTGT	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59026460	TTCAGTATTGAAACA[-/GTGT]GTAACAGCAAGCCAT	54778
rs560734511	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59075884	GGTTATATTAGGAAT[A/G]CTTTTATAATATAAC	54778
rs560736408	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59082751	CACATAACCTGTTTG[C/T]CAAACTCTTGATCTA	54778
rs560797190	snp	A/G	0	0	intron-variant	RNF111	GRCh38.p7	15:59082205	ACAAGTTTATACCAG[A/G]TTATTTAGTAAAATC	54778
rs560797537	snp	C/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59025724	CCAAGTCATCTATGG[C/T]TTTTTTTTTTTCTTT	54778
rs560831323	in-del	-/AA	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:58991129	AACCCCGTCTGTACT[-/AA]AAAAAAAAAATACAA	54778
rs560875640	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59064707	AAGAACCTTTACAAA[A/C]GGGTTTGGGAGATTA	54778
rs561006705	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59045464	AAAGTGCTGGGATTA[C/G]AGGCGTGAGACACTG	54778
rs561032059	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59039294	TATCATTTTGCTTAG[C/G]TTTATTATCTGAGGT	54778
rs561032789	snp	C/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59076728	CAGCCATGCCTTTTC[C/T]AAAGAAATTGAAATT	54778
rs561033295	snp	C/G/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59049902	GCGTGCCACCACACC[C/G/T]GGCTAATTTTTGTGT	54778
rs561066368	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59048096	AGAACCTAGAAATTA[C/T]ATTCCTAAGTATTTA	54778
rs561068948	snp	A/C	0.079617	0.182947	intron-variant	RNF111	GRCh38.p7	15:59051787	AATAAATAAATAAAT[A/C]AATAAATAAATAAAT	54778
rs561095565	snp	A/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59003572	CCCAGCTAATTTTTT[A/T]AAAATTTTTTGTAGA	54778
rs561117899	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59070693	AGCTCCTCCTTTTCT[C/G]TTTCCCAACTTGAGT	54778
rs561143386	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59062195	CTACAGGCACACTCT[A/G]CCACACCTGGCCAAT	54778
rs561174751	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59088856	GAAACTTATTCTCTC[C/T]ATAAGGTGTATGACA	54778
rs561219775	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59083537	TAGACTTCCTCTCCA[A/G]AAAAAAAAAAAAGTA	54778
rs561224574	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020460	CCAGATACTGTTCAG[A/G]CTTGTGAGGTTAGAT	54778
rs561234116	in-del	-/T	0.00478085	0.0486577	intron-variant	RNF111	GRCh38.p7	15:59042429	TATGGCTGTCCAACA[-/T]TTTTTTTTCACAAGT	54778
rs561236225	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59008508	ACAGGCGTGAGCCAC[C/T]GCACTCAGCCTACCA	54778
rs561237724	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59038753	GGTAGGTAGTTGGGT[C/T]TAAAAGCTTGATTAG	54778
rs561251742	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59087715	AGTAGGAAAAGGAGG[A/G]ATTCATCTTGCTGTC	54778
rs561270825	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59025204	ATCAAGTTTATCTTA[A/T]AGTTTCATAGCAGTT	54778
rs561279242	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59014755	ATTAACAGGAATTGC[A/G]GACTTTTTTTTTTTT	54778
rs561281221	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59068078	TTATGTCACTTCCAT[A/G]TACGATTATGATATA	54778
rs561314888	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59037607	TTTGGGAGGCCAAGG[A/C]AGGTGGATCACCTGA	54778
rs561323947	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59074951	GTCTCAGGGAATAGG[A/G]AGGCCCAAAGAGAGG	54778
rs561346807	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021187	ATGAAGTCTTGCTCT[G/T]TTGCCCAGGATGGAG	54778
rs561431003	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59039613	CCTTTTGATGCCATC[C/G]TAGTAGTCGTTGATA	54778
rs561431185	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59013945	AGGCACACGCCACCA[C/T]GCCTGGCTAATTTTT	54778
rs561483426	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59061681	TTATCTGTGCTCTAC[C/T]TCTTATCCTTTCCTT	54778
rs561493273	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59043662	TGGGTACAAATCTTT[A/G]TGTACATATATGTTT	54778
rs561498569	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59032024	GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA	54778
rs561507924	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58996635	GTATGTGATTGAAAA[C/G]TCATCAGTACTTTCT	54778
rs561518462	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59013446	TGTCAAATATTTTAT[A/G]GACCATCCCTGAATC	54778
rs561541114	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59068198	GCACTCCAGCCTGGG[C/T]GACAGAGTGAGATGC	54778
rs561555302	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59019056	AGCCACCCGTGTAGG[C/T]GAGACTTCAGGCACG	54778
rs561557706	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59012992	GATCCACCTGCCTTG[G/T]CCTCCCAAAGTGCTG	54778
rs561575945	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59007840	ATTTTTTGTGGGGTT[A/G]TGTTATTAGAATATA	54778
rs561580075	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59093820	AAATTGTCTACCATA[C/T]GACAAATAAGGTTTT	54778
rs561580286	snp	A/G			utr-variant-3-prime	RNF111	GRCh38.p7	15:59097408	TGTGATAAACTGATC[A/G]TTTGAAACGTTTTTC	54778
rs561608459	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59050385	TCCTTTGTGTTTGTC[A/G]TCTTGGTGAATTATT	54778
rs561623124	snp	A/G			utr-variant-3-prime	RNF111	GRCh38.p7	15:59097242	AGTGGTAGCTGTCCA[A/G]ATACATAAAAACTAA	54778
rs561648149	snp	A/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59018538	TTCAAAATTGGTAAA[A/T]GGTTACTTTTTAGAA	54778
rs561683432	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59086184	GAGTGCAGTAGTATG[A/G]TCTCAGCTCACTGCA	54778
rs561694411	snp	A/G	0.0119091	0.0762411	intron-variant	RNF111	GRCh38.p7	15:59047324	AACATATGAGATCTC[A/G]TTTGTATGAAAAATT	54778
rs561704489	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58988854	TGCGGCATTAATTTA[G/T]AATTCTCTTGAATGG	54778
rs561715106	snp	G/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59080157	GTGGAGTCTCACTCT[G/T]TCGCCCAGGCTGGGG	54778
rs561717267	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59086140	TTTTCTTTTTTTTTC[A/G]ACAGAGTCTCACTCT	54778
rs561788406	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58994321	TGGGATTACAGGCGT[A/G]AGCCACCACGCCTGG	54778
rs561800149	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59043058	TATCTTGCAGAGAGC[A/G]TTTTATGTTCTTTTA	54778
rs561804336	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59007393	TTAATCCGTATTGAT[A/G]CATGTATCAGTAGTT	54778
rs561834588	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59093164	GGAAATATACTGCCT[A/G]TTGTAGGGCCACACA	54778
rs561856564	in-del	-/TG	0.0142736	0.0832652	intron-variant	RNF111	GRCh38.p7	15:59072826	CTTTTGCTGCAGTTT[-/TG]TTTGTTTGTTTGTTT	54778
rs561881606	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59055043	CAGTGTAATGCCACA[C/T]ACATACTTAAATGAA	54778
rs561922082	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59078757	GCAGCTACTCGGGAG[G/T]CTGAGGCAGGAGAAT	54778
rs561985476	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF111	GRCh38.p7	15:58988284	TACCGACACACCCAC[A/G]GCCTACAGTGAGGGA	54778
rs561990468	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59060842	GGTCTGACTCTGTTG[C/T]CCAGGCCTGTGTGCA	54778
rs561994226	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59084742	AAGCTTTGTACCCAT[C/G]GACCAGCATCTCCCC	54778
rs562004006	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59072642	ATTTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGA	54778
rs562015902	snp	C/G			upstream-variant-2KB	RNF111	GRCh38.p7	15:58985725	TCCAAAATATTATTT[C/G]AACATATAATAAATA	54778
rs562050251	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59024630	GAGTGACTTTACTAG[C/T]CTTTCCAGGATAATG	54778
rs562100110	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59078745	GTGCCTGTAATCGCA[A/G]CTACTCGGGAGGCTG	54778
rs562118715	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58993127	GTGAGCCAAGATTGC[A/G]CCACTGCCCTTCAGT	54778
rs562135909	snp	A/C/T	4.80969e-05	0.00490373	intron-variant	RNF111	GRCh38.p7	15:59030776	AAACACATTAAAAAT[A/C/T]TTTTAAATATCTAAT	54778
rs562152819	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59036672	GGACAAAGCCAAACC[A/C]TATCGGTGCATCAAT	54778
rs562161584	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59007398	CCGTATTGATACATG[G/T]ATCAGTAGTTCCTTC	54778
rs562166798	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59036147	GTGGTGTGATCTTGG[C/T]TCACTGCAACCTCTG	54778
rs562204643	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59017435	ATGGTTTAATTTTAC[A/G]TTTACCTGTTACAGA	54778
rs562267792	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59065456	TACTGAGAAATTTAT[C/T]TTTTCTAACAACCAT	54778
rs562286579	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59047493	GATCAAGACACTTTC[A/T]CAAACACAAACAGAC	54778
rs562332767	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59064916	ACCAAGCAGAGCCTG[A/T]AGCACCCCCCTACCC	54778
rs562337374	snp	A/G	6.60546e-05	0.00574656	missense	RNF111	GRCh38.p7	15:59058547	ACTGGCACTTCTATA[A/G]GAGGTATGTAAAAAA	54778
rs562351673	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59059016	GGTGTGATGGCTCAT[A/G]CTTGTAATTCCAGTA	54778
rs562351703	in-del	-/G			intron-variant	RNF111	GRCh38.p7	15:59032053	AAGCAATTCTCCTGC[-/G]TCAGCCTCCCAAGTA	54778
rs562367531	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59035317	CATATTTCAAAACCA[A/G]TCATGCCTTCCCAAC	54778
rs562395707	snp	A/G	0.00478085	0.0486577	intron-variant	RNF111	GRCh38.p7	15:59017979	GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG	54778
rs562442448	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59054127	TATTTTTAGTAGAGA[C/T]GGGGTTTCAGCATAT	54778
rs562498690	snp	A/G	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:59059699	CAAGCTAGTTCTTAC[A/G]TTTCAATTAGCAGTG	54778
rs562502619	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF111	GRCh38.p7	15:58987160	ACGCATTTGTTATCT[A/G]CTGACTTTTATAAAA	54778
rs562505307	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59046833	ATATCTGAGAAAAGA[C/T]TTGTATTCAGGATAT	54778
rs562515456	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59023001	CCTGTAATCCCAGCA[C/G]TTTGGGAGGCCGAGG	54778
rs562581244	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:58999310	ATTTTAATAAAAGTT[A/T]CTTATATTAGATATA	54778
rs562603569	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59034821	CTAAACTTTTAATTT[C/G]ACTTATTTACTACAT	54778
rs562606016	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59077351	TTTAGATTCATTTGT[C/T]ATATTCTAAAACATT	54778
rs562606401	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59022720	TTTTAAATGCAACCA[A/G]AAGACTCACCAAAGT	54778
rs562635591	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59093020	AAAAAAAGAGTAAAA[A/G]TAAACTGGAAACCAA	54778
rs562638956	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59064362	AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT	54778
rs562639121	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59029081	CACCGCGCCCAGCTT[G/T]TATTTAATTTTTGAG	54778
rs562670018	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59016115	GTGCTAGGATTACAG[A/G]CATGAGTCACTGCTC	54778
rs562706406	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59078014	TTTTTCATCCAGAAT[G/T]AACTGGGGAAGACAA	54778
rs562714326	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58992096	GTTGCCCAAGCTGGA[A/G]TGCAGTGGTGTGATC	54778
rs562720849	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59048241	ATGGATAAAGTATGT[G/T]ATATCCATATGATTG	54778
rs562758052	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59015617	ACCCTAGCTTATTCT[C/G]CCCTACTAAAAAAAA	54778
rs562788275	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59016635	CTACCTATTTCAAAC[A/G]GTATTTCCTGCCTCT	54778
rs562818078	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59045468	TGCTGGGATTACAGG[C/T]GTGAGACACTGCGCC	54778
rs562832815	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59009590	TAGATAATATAGAAC[A/G]ATACCAAAATTAGAA	54778
rs562839820	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:58998146	CTGACCTCGTGATCC[A/G]CCAGCCTCGGCCTCC	54778
rs562847461	snp	G/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59083481	AGGCAGAGGTTGCAG[G/T]GAGCCAAGATTGCCA	54778
rs562865599	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	RNF111	GRCh38.p7	15:59096971	ACTACCTGTTGACTT[C/G]TTTTATAATTGCTAC	54778
rs562868610	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59004227	CTTCAATTTAAAATA[C/G]TCCTTCTTTTCTCTC	54778
rs562879108	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59052561	GTATGCATATATCAG[A/C]TTAGTGGATTTTTTT	54778
rs562891106	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59058283	TTAATTATAAACACA[A/T]TAGCTTACATTAAAA	54778
rs562905835	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59010171	TGAACATTGTTTTAT[A/G]CTGCTAATTATATAT	54778
rs562916748	snp	G/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:58989605	ACCAGACATAGAACT[G/T]GTTTTTAAAGAAAGG	54778
rs562918559	snp	C/G	1.64836e-05	0.0028708	missense	RNF111	GRCh38.p7	15:59089673	TTGAAATAGGTTCCT[C/G]ATATGGCAGGCTATC	54778
rs562932652	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59089027	GTAGGAGCTCAAATA[C/T]GGCAGAGCCCTGTTC	54778
rs562960830	snp	C/G	0.00119737	0.0244387	downstream-variant-500B	RNF111	GRCh38.p7	15:59097617	ACTGTTACTTGTTCA[C/G]GCCTGTAATCCCAGC	54778
rs562984430	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:58997422	GGTGCAAAAAACAGT[A/G]GTGCATTAAACTAAT	54778
rs562998844	in-del	-/T	0.0103295	0.0711199	intron-variant	RNF111	GRCh38.p7	15:59090229	TTGTTTGTTTGTTTG[-/T]TTGTTGTTGTTGTTT	54778
rs563020786	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59002812	TAGTTCTTTGCACCT[A/G]TTAGGCATATTCCTG	54778
rs563023004	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58996868	GTTTCAAAAGACTTA[A/C]AATGAAAAACAGTGG	54778
rs563035310	snp	C/T	0.000131798	0.00811675	missense	RNF111	GRCh38.p7	15:59081020	CTCAGACTCAGCCTC[C/T]GCCTCAAGTGGATTA	54778
rs563071190	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59079082	GGGAAAGGGTTTTTG[G/T]GAATGTGGAATATGT	54778
rs563083347	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59017518	AAAACATCAATTGTC[C/T]TTAGGTTTGGCTTCT	54778
rs563111570	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59002332	CAGGTTTTTCCTTTA[C/G]AATTAATAGCTGTCC	54778
rs563112812	snp	G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59033502	GGGAAATGAGGAGTT[G/T]TGTTGCTTAATTGTC	54778
rs563147170	snp	C/G	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59027599	AATGGCGCAATCTCG[C/G]CTCACTGCAACCTAT	54778
rs563171399	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:58992980	TTGAGACCAGCCTGC[C/G]CAACGTGGCAAAACC	54778
rs563230023	snp	C/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59014785	TTTTTGAGACAGGGT[C/G]TTCCTCTATGGACCA	54778
rs563232601	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59090316	CTCACTGCAACCTGC[A/G]CCTCCTGGGTTCAAG	54778
rs563265213	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59094140	AACAAATCATTACAT[A/C]TCCTTTTAACTTACC	54778
rs563290738	snp	C/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59000548	GAAACCCTGTCTCTA[C/T]GAAAAATACAAAACA	54778
rs563297032	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59062643	CCTATAGTGTTGGCC[G/T]GTGGATTTGCCTATA	54778
rs563413156	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59051192	GGTGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	54778
rs563420080	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59028078	GTGATCTGCCCGCCT[C/T]GGCCTCCCAAAGTGT	54778
rs563423466	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59014613	AGGGGCAAGCACATA[A/G]GGGAAAGTTGTTAGA	54778
rs563459340	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59025952	TCAGGCTGGTCTCGA[A/G]CTCCCAACCTCAGGT	54778
rs563471229	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59068092	TGTACGATTATGATA[C/T]AAGTCTGCGTGTTGC	54778
rs563474663	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59056930	TTACAGTAAGTTCAA[C/G]CAGAATTTACACTTT	54778
rs563475953	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59081502	TTGTTTTCTTTTTTT[A/G/T]AAAAAAGAACAAAGA	54778
rs563533883	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59067741	ACTTTAAACAAATTG[C/T]TGAAACTCTAGTGTC	54778
rs563601615	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020289	TAGTAAATATGCATT[A/G]TATATTGTAATATAT	54778
rs563639342	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59050549	GTTTCAAAATGGACC[A/G]TAAAATACGTGTAAT	54778
rs563657263	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59050125	GCTGGAGTGCATTGG[C/T]GTGATCTCGGCTCAC	54778
rs563671631	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59032079	AAGTAGCCAGGATTA[C/G]AGGTGCCCACCACCA	54778
rs563686467	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59019765	GGAATTCGAGACCGG[C/G]CTGGCCAACGTGGTA	54778
rs563699604	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59042472	CTTTTATTCTTACTG[C/T]TTCTGGATTTTGAAT	54778
rs563725527	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59026018	TACAGGCGTGAGCCA[C/T]TGTGCCCGGCCGGCT	54778
rs563794911	snp	A/T	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59090625	TACTAGAATTATTTC[A/T]TCTTCTCCATACATA	54778
rs563813463	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59018566	GAAAAAAAACAAACT[A/G]TATATACAGAAACTT	54778
rs563838693	snp	A/G			downstream-variant-500B	RNF111	GRCh38.p7	15:59097633	GCCTGTAATCCCAGC[A/G]CTTTGGGAGGCTGAG	54778
rs563857335	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58989696	GAATTTCACTTTGGT[A/G]CTCCATTTCTACAGA	54778
rs563891283	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59007192	ATTGAACACGAACAA[C/T]CATGACCTCAAAAAG	54778
rs563910488	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59073627	GTCTTCACGACATCT[A/G]TAGTTACTTCATCCA	54778
rs563912984	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:58995260	GTGTTTATTTTGTAA[C/T]TCATCCATTTTCTTC	54778
rs563957344	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59024500	GAATATGAGTTTGAG[G/T]GATGAGGAAGAGAGG	54778
rs563975222	snp	C/T	0.0425829	0.139564	intron-variant	RNF111	GRCh38.p7	15:59080113	GCCTTCTTGTGTGCT[C/T]CTTTTTTTTTTTTTT	54778
rs563999666	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59073374	TAATCCCAGCTGCTC[A/G]CGAGGCTGAGGTAAG	54778
rs564023309	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59066412	GGTTGGGAGTTCAAG[A/G]CCAGCCTGACCAACA	54778
rs564072241	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59006717	AATAAAGTTACAGAC[A/G]CCAGTGCATTTTACC	54778
rs564117286	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59093103	GCTTCATCTGGCGAG[G/T]GAAACAATAAAAGAT	54778
rs564138902	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59018097	ACTTTCCATTAATGC[A/G]GCAATCATAATTATT	54778
rs564142811	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59060007	AAGTATTCTCTCCCC[C/T]GGAAAACTGAGGGCA	54778
rs564153077	in-del	-/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59088788	TTAAAAAATATTGTA[-/G]GAATCATTAACATTG	54778
rs564178225	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58999877	CAAGAGTAGGTGTCT[C/T]ACATGGCAGGAGCAG	54778
rs564219928	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59006021	AAGTCACTATTTCTG[C/T]ATTTCCTTCTAAGGA	54778
rs564269450	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59017530	GTCTTTAGGTTTGGC[A/T]TCTATCACTTTAAAA	54778
rs564292183	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59017190	TGTCTTCTACGAATC[C/T]GTTCCCTGGTGCCAA	54778
rs564302105	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59060790	CTTTATGTAGCATTA[C/T]TATTATTATTATTAT	54778
rs564321774	snp	C/T	0.000117358	0.00765933	intron-variant	RNF111	GRCh38.p7	15:59091190	ACTTCTGGAGTGTTA[C/T]TGAAAGGCATAAATG	54778
rs564384430	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59090390	GCCCGCCACCACGCC[C/T]GGCTAATTTTTGTAT	54778
rs564389666	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59029109	GAGGATCTGCTAGAC[C/T]GCTTCCCAAAGTAGC	54778
rs564393100	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59078074	TTGGATAGATTCGAG[G/T]TGACCTCCCAGCTCT	54778
rs564458457	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	RNF111	GRCh38.p7	15:59097752	GTCATGGGTAGCGGG[G/T]GCCTGTAGTCCCAGC	54778
rs564465619	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59072523	CAGTGGCGTGATCTC[A/G]GCTCACTGAAAGCTC	54778
rs564478117	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59059164	AACAAAAAGCCCCAA[C/T]CCAACAGAAAGACAA	54778
rs564504768	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59084352	TTGCAGAAGGATGAT[A/G]TGGAGAAACCTAATC	54778
rs564511757	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59012859	TTCTCCCACCTCAGC[C/T]TCCCAAGTATCTGTG	54778
rs564512288	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59078679	GCCTGGCCAACATGG[C/T]GAAACCCTGTCTCTA	54778
rs564557891	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59041754	ATGCTCACCGGCAAG[A/G]GTGCCTGTTTTCTCA	54778
rs564601372	snp	C/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59050500	AAAAGTAGACTTACC[C/G]TGACACTAGACTCTA	54778
rs564620093	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59047881	TATCCAGCCTACTTA[A/C/T]TTTAGAAATGGTTAT	54778
rs564640918	in-del	-/TA	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59046763	TGCTTCAAAAGACAC[-/TA]TTAAGAAAATGAAAA	54778
rs564644208	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59034674	TTAACTTCCTTAGAT[A/T]CTTAGGAGATAGGTT	54778
rs564656756	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:58997561	TGGTGTCTCACGCCT[G/T]TAATCCCAGCACTTT	54778
rs564665683	in-del	-/TATTT	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59008948	GTTAATATTGTCACG[-/TATTT]TATTTTATTTTATTT	54778
rs564721267	snp	C/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59077009	TCTGCATCGTGCAGA[C/T]GCAGCTGGAATCAAC	54778
rs564735705	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59064793	TAGAGCTACTGTGTA[A/G]CAGAGGTTAGAGCAC	54778
rs564746196	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59010449	CTCTGTCGCCCAGGC[C/T]GGAGTGCAGTGGTGT	54778
rs564781639	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59037227	TTATTAGGGATTTCT[A/G]TTATGTGTAGAAAGC	54778
rs564782312	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59076606	GGCTCACTCCTGTAA[C/T]CCCAGCACTTTGGGA	54778
rs564805541	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59053361	GAGTTGCTTTGTTAC[A/G]TTTGATACACCCAAC	54778
rs564836048	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59059563	AAAATTTTGGTGATA[A/T]CCATTTTCTGGGGTT	54778
rs564892272	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58991536	GGACCATGTGATACG[A/G]CATGGATGGAAGTGG	54778
rs564896572	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59045485	TGAGACACTGCGCCC[A/G]GCCTTAGTTTTTCCT	54778
rs564896855	snp	A/G	4.99854e-05	0.00499902	missense	RNF111	GRCh38.p7	15:59052431	TTGGAGAAAGCTATC[A/G]GTGAGATTTTAATTC	54778
rs564962449	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59051936	TAATTACTTTGAGCT[A/G]TTAAAGGGTTAATAT	54778
rs565009069	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59025280	TTATCAAGGGTCCCA[C/T]TCTTCTTTTCATAAT	54778
rs565015898	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58992068	TATTTTATTTTGAGA[C/T]GGAGTTTCCCTCGTT	54778
rs565029264	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59037975	GTTTTGTCTATCTTG[C/G]TTTGAAATACAAAGT	54778
rs565065069	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59069911	ATTAGACTGGCATAC[C/T]GAGAAGATGCAGTAG	54778
rs565075874	in-del	-/C			intron-variant	RNF111	GRCh38.p7	15:59013134	GTCACTCATTTCTCT[-/C]CTGCCTTTCCTAGGG	54778
rs565096121	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59040504	AAATCTTTAATTTAA[A/G]TGAATATTTCCACTG	54778
rs565131751	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59083341	TCACAAGGTCAAGAG[A/G]TTGAGACCATCCTGG	54778
rs565151759	snp	A/G	0.00358779	0.0422022	utr-variant-3-prime	RNF111	GRCh38.p7	15:59095227	GCTGCTTTAGTAAGT[A/G]GAATTTTGTGGTCTT	54778
rs565157563	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58999440	CCCCAGGTTCAAGCA[A/G]TTCTGCTGCCTCAGC	54778
rs565180999	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58993162	GTGACAGAGCAAGAT[C/T]CCATCTCAAAAAAAA	54778
rs565254319	in-del	-/TA	0.0126979	0.078662	intron-variant	RNF111	GRCh38.p7	15:59011953	CAAAGATTCCTAGCT[-/TA]TATATAAGAATAAGT	54778
rs565263646	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021220	CAGTGATGCGATCTC[A/G]GCTCACTGCAAACTC	54778
rs565298887	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59057137	TTTTTGGTTTTCACA[A/G]TTAGGGGAGGATGCT	54778
rs565317048	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59032214	AAAGTGATGGGATTA[C/T]AGGCATGAGCCACTG	54778
rs565324248	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096876	GTATGTCATGGAGTC[A/C]TCTTGACGTTCCCCC	54778
rs565353171	in-del	-/ATT	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020266	TATAACAATATATGC[-/ATT]ATATATAGTAAATAT	54778
rs565485529	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59069519	CTTGAGTCAGTTGTA[A/G]GTAGGATCTCTTTTA	54778
rs565490621	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020529	GTCATTGCTAGAGCA[A/G]TAGACTCTGTAACAT	54778
rs565550153	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59075717	TTATGCTTGATTTTT[A/T]AAAATTGGTTTAACT	54778
rs565600269	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59084686	TTCACTGTAGTCACC[A/G]TGCTGTGCAGTAGAA	54778
rs565621697	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59008825	TCTTTTAGGGTTTAC[A/G]CTATGCATCTTTGTC	54778
rs565628794	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59006942	AGGCGCCCGCTACCA[C/T]GCCCAGCTAATTTTT	54778
rs565632013	snp	A/G	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:58990293	GTTGTGTTTGTCGTA[A/G]TTGAATCCCCAGAAA	54778
rs565632190	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59029657	ACAGCTGTTGTACTC[A/G]CTTTTTAGGAACTGG	54778
rs565634961	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59079379	GAGTAAAGCATTGAT[C/T]TGAAAACAGAACTTT	54778
rs565637042	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59054522	ATGGTGGTATCTTTC[C/G]TCATACAAAACCATT	54778
rs565639814	in-del	-/TAT	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59017068	CGGTGAATTGTATAA[-/TAT]TATATATTGCAATGC	54778
rs565657948	snp	A/G	0	0	intron-variant	RNF111	GRCh38.p7	15:59080170	CTGTCGCCCAGGCTG[A/G]GGTGCAGTGGCATGA	54778
rs565672537	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59077482	GAAATTTTCTTTGTA[A/C]ACATAGATAGGTATA	54778
rs565684190	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59037684	TCTACTAAAAATACA[A/C]AATTAGCCGAGCGTG	54778
rs565696296	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59043163	AATTTAGTAATTTTT[A/T]TTTTTTTTTGAGACA	54778
rs565729193	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990025	AAATGATAGCAGTTA[A/G]AATATGTTATAACTT	54778
rs565737840	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59073886	GAAAGTTGAAATTAC[C/T]CCTTGATTCATAGTC	54778
rs565751333	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59012304	GATTACAGGCGTGAG[C/T]CACTGCACCTGGCCT	54778
rs565767512	snp	A/G	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59086175	CCCAGGCTGGAGTGC[A/G]GTAGTATGATCTCAG	54778
rs565887113	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF111	GRCh38.p7	15:58988337	CCCACTTCCGACTCT[C/G]CCTAGAGTCTCAGGA	54778
rs565902264	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59050019	TGCTGGGATTACAGG[C/T]GTGAGCCACCACGCC	54778
rs565946428	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59060997	TTTTGCCATGTTGCC[A/G]TGTTGCCCACACTGG	54778
rs565956874	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59085408	TAGCCATATATTTCC[G/T]TCCTTTGTAAGATGT	54778
rs565979498	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59072654	AGACGGGGTTTCACC[A/G]TGATAGCCACGTTGG	54778
rs565984788	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59092433	AAAGTGCGGGTGAAT[A/G]TGTGGTTTTGTTTTG	54778
rs565991732	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59078864	TCTCCCTCTCAAAAG[A/G]AGAAAAAAAAAAAAA	54778
rs566011411	snp	C/G	1.77656e-05	0.00298035	intron-variant	RNF111	GRCh38.p7	15:59067129	CTGCCCCTCTTGTCT[C/G]TCTCTCTCTCTCCTT	54778
rs566051741	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59078281	AGAATATGTCTCTCT[C/T]TGCTTTTGAAAGGTT	54778
rs566091216	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59054596	TGTTTCTGATATGTA[C/T]TATCCTATGTTGACA	54778
rs566119544	snp	G/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59018181	TTCGAGCATTAAAAT[G/T]TATTTGTAAAGATGG	54778
rs566227207	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59000088	GACACAGATCCAGAC[C/T]ATATCAATAAGTATC	54778
rs566245737	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59066510	AGCTACTCAGGAGGC[C/T]GAGGGAGGAAAATCG	54778
rs566256678	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59030163	AACTGAATGATCTTC[A/G]GCAGCCCACAGTCTT	54778
rs566260945	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59084778	TCATTCATGACCCCC[C/T]ACCCTCTCCCCAGCC	54778
rs566262018	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59053872	TTGTTATATCTCTTA[C/T]TGTTATTAAGAGATA	54778
rs566266083	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59071637	GAGGTGGAGCTTGCA[A/G]TGAGCCAAGATTGTG	54778
rs566325369	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59053524	GAACATGCTTTTCCA[C/T]TTGCCATTTTAGCAT	54778
rs566358844	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59036256	AGAGACTGGGTTTCA[C/T]CATGGTGGCCGGGCT	54778
rs566380991	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59035628	TCTGCTTCCTCTCGA[A/G]TGGTTTGCTCTTAGA	54778
rs566399448	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59050418	AAGATGGTGGTTTCT[A/G]GCGAAAGGCCAGATT	54778
rs566422280	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59041524	AGAGATTGTGCCACT[A/G]CACTCCAGCCTGGGT	54778
rs566437056	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58999525	ATTTTTAGTAGAGAC[A/G]GGGTTTCACTATGTT	54778
rs566474159	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59028446	TAGGCAGAATAAGAG[A/G]CTAACAACAACAATA	54778
rs566484337	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59005552	ATTTTGTTACTCCAA[C/G]CTTTGCTTTGGCCTT	54778
rs566509487	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59034931	ATTAATCCATTGTCA[C/T]GCTGCTAATAAAGAC	54778
rs566553760	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:58993339	CATGGTGAAACCTTG[G/T]CTCTACTAAAAACAC	54778
rs566606736	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59010960	TGCTCAAAAGTGTCT[A/G]AAGAAGTCATCTAAT	54778
rs566627135	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59038394	AGTTTGCTTAAAAAG[A/G]TAACCCTTGGAATTG	54778
rs566677646	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59014237	TGTGTTTCTTTACTT[A/T]CTGGCACTACCAGAT	54778
rs566680116	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59016966	AGAATCTAATGCCTG[A/G]TGATCTGTCACTGTC	54778
rs566716188	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59051263	TCGCGACCATCCTGG[A/C]TAACACAGTGAAACC	54778
rs566717443	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59022759	CAGATAATAGGAAAC[C/T]TCTCATTATTAATAT	54778
rs566726083	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59065380	CTTCTGCCATAGAAG[A/C]ACATACCTTCAAAAT	54778
rs566734653	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59064548	CGCAAAAAAAAAAAA[A/G]AAAAAGGAAATAATT	54778
rs566746078	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59017097	ATGCAATGATAATAG[A/G]AACAAAGTGCACAAT	54778
rs566797361	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59040580	GTATTTGTTCTTACA[C/G]TGAAAACTCTGATTC	54778
rs566824353	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF111	GRCh38.p7	15:58986541	TTTTTCTTGGAGACG[A/G]AGTCTCCCTGTCACC	54778
rs566844927	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59071356	CTTTGCTATAGAGTA[C/G]AGGTGAAAGTGTTTT	54778
rs566856317	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59015732	TCGCCCACCGTCACC[C/G]TGTGCATCCTTCATG	54778
rs566882392	snp	C/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59036220	GCACCACCACGCCCA[C/G]CTAATCTTTATATTT	54778
rs566908833	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59039524	GATGGGTTTCAGTTT[G/T]TTGCAGTCTTTTTAT	54778
rs566916959	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59087238	TGTGCAGAGTGACAA[G/T]AGGGTGAAAAAACCT	54778
rs566918379	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:58991620	CCTGTGACTTCAATG[A/G]CTAGAAAAAATCAGC	54778
rs566919575	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59077492	TTGTACACATAGATA[A/G]GTATATGTCTTACCT	54778
rs566924359	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58997700	ATATGTCTGTAATCC[A/C]AGCTACTCGGGAGGC	54778
rs566929814	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59076718	AAAATAGAACCAGCC[A/G]TGCCTTTTCTAAAGA	54778
rs566988749	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59084642	TTAAAATCTTTTGTC[A/G]CAGTTTTGAAATAAA	54778
rs566998890	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59039925	TTTCACCGTGTTGGC[C/T]AGCATGGTCTCGATC	54778
rs567003886	in-del	-/TTTA	0.00358779	0.0422022	upstream-variant-2KB	RNF111	GRCh38.p7	15:58985831	CACTTCTCAATTATT[-/TTTA]TTTATTTATTTTTTT	54778
rs567029351	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59003818	GTGGCTGATGCCAGT[A/G]CCTAAAACAAGTGCC	54778
rs567052930	in-del	-/T	0.0023933	0.0345097	upstream-variant-2KB	RNF111	GRCh38.p7	15:58985842	ATTTTTATTTATTTA[-/T]TTTTTTTAGGGAGAC	54778
rs567082660	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59089097	AATTTTTTGCCACCG[A/G]TCATATCCACGAATG	54778
rs567087928	snp	A/G	0.0193772	0.0965046	intron-variant	RNF111	GRCh38.p7	15:59022959	ATCTTTGAAAGTGAG[A/G]AAATTGGCTGGGCGC	54778
rs567090812	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59052699	ACTGTAGGCACATGT[C/G]ACTAAGCCTGTCTAG	54778
rs567169325	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990379	GTCATGAAGCTGTGG[A/G]CCAGGCGTGGTGGCT	54778
rs567171008	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59075355	AACTTTTTTTATTCT[C/T]ATGTTTTTGAACAAG	54778
rs567179981	snp	C/T			upstream-variant-2KB	RNF111	GRCh38.p7	15:58987089	GACTTTGAAAGGAAG[C/T]CTGCCTGATGGACTC	54778
rs567206095	snp	G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58996251	AATCTGAAGAAAACT[G/T]TTGCTTTTTAAGAAA	54778
rs567223230	in-del	-/TT	0.458545	0.137872	intron-variant	RNF111	GRCh38.p7	15:59049363	TCCAGGTGTCTTTGA[-/TT]TTTTTTTTTTTTTTT	54778
rs567265859	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59057926	AGTGGTGAAATCAGT[A/T]TTGCTATCCAGGCAG	54778
rs567282887	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59073981	GGTGACTATGTGCAT[C/T]GTCAAGAAACAGCAA	54778
rs567293385	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59026767	CAGCGATGGATTTTA[A/G]AAAAAAAAATAGTAT	54778
rs567398132	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59049161	TCCAAAACTGGAACT[C/T]TATAGCCATTATACA	54778
rs567455566	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59056632	ATATACAATCAGCTC[C/T]TCTATGGGCTATTTG	54778
rs567516636	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59056035	AATTCTTTGTGGTTA[C/T]TGTTTCAATACTTGA	54778
rs567519144	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59032088	GGATTACAGGTGCCC[A/T]CCACCATGCCCAGCT	54778
rs567523588	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59001891	TAAAGTTTAATTTAT[A/G]CATTGGGCAGAGTAA	54778
rs567534386	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59002415	CTTTATTAGAACATT[C/T]TTATGTGAGGGACAA	54778
rs567537332	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59032446	TGTTTTTTTGAGGCA[G/T]CATCTGGCTTTGTTG	54778
rs567547642	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59039033	GCAATGACACGATCT[C/G]AGCTCACCGCAACCT	54778
rs567593321	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59044570	GTAGCCAGAGAAATA[C/T]GTTATTTTTCTCATG	54778
rs567605739	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59068039	GTAAAAGAAGTCAAG[C/T]GTTCCATGCTACTTT	54778
rs567627370	in-del	-/CAG	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59030162	TAACTGAATGATCTT[-/CAG]CAGCCCACAGTCTTG	54778
rs567636147	in-del	-/AGTG			intron-variant	RNF111	GRCh38.p7	15:59023262	CAAAGAAAAAAAGAA[-/AGTG]AGGAAGTAGCATGCT	54778
rs567649579	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59067814	TTTTACCTCCTACTG[-/T]TAGAGTTCACTATAA	54778
rs567663832	snp	C/T	8.25962e-05	0.00642583	missense	RNF111	GRCh38.p7	15:59031469	CATGCAGAAAGAGAT[C/T]TGTAAAAAATAATTC	54778
rs567670074	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59008070	TCCTGTGAAATCTTT[G/T]CCCATGATATAATCA	54778
rs567671377	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59043348	TTTGGTAGAGACGGG[G/T]TTTTCACCATGTTGG	54778
rs567687684	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59065594	GACTCCATGTTTCTT[C/T]TCCCACTGTGTGACA	54778
rs567698752	in-del	-/TCCC			intron-variant	RNF111	GRCh38.p7	15:59067262	TTTTTTTTAACTCCC[-/TCCC]ATTCTTCCTTCCTTT	54778
rs567735579	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58998064	CCCGTGCCACCACAC[C/T]CGGCTAATTTTTGTA	54778
rs567748226	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59007527	AAAGCGATGAACATT[C/G]ATATACAAGTCTTTG	54778
rs567769974	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59089008	AACAAGACACTGGTT[C/T]ATAGTAGGAGCTCAA	54778
rs567781200	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59050151	CTCACTGCAATCTCC[A/G]CCTCCTGAGTTCCAG	54778
rs567792556	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59013822	AGACAAGAGTCTCAC[C/T]CTGTTGCCCAGGCTG	54778
rs567795116	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59037088	GTGATGTGCCTGCCT[C/T]GGCCTCCCAAAGTGC	54778
rs567801014	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59013795	TATTCATTTTTTTTC[-/T]TTTTTTTTTGGAGAC	54778
rs567817886	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59091716	ATGCTCAATACCAAC[A/G]GTCCCCAACCTTTTT	54778
rs567822434	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59025562	GTAAAATAAATAAGA[A/G]AATTAAAAATTTAAT	54778
rs567847664	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59037895	CAAGGAAACGTAAAT[A/G]TCAAATATGCTCCTA	54778
rs567852479	snp	A/G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59056643	GCTCTTCTATGGGCT[A/G/T]TTTGCAGTTTGGGTG	54778
rs567856353	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59042511	GGAATACTTTTACCA[C/G]TCCAAAGTTCTAGCA	54778
rs567882008	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59071702	CGCAAAAAAAAAAAA[-/T]AAATAAAGTTTTTGG	54778
rs567890610	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59052779	AAAATAAAGCTATAT[C/T]GTTGCCCAGACTCTT	54778
rs567914742	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59018891	TTTGTTTCTGCCCTC[G/T]TATTTGTGCATATAA	54778
rs567929194	snp	C/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59020190	TGCAAATATACTATA[C/T]ATTTTGTAAGATACT	54778
rs567951174	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59073801	TCAATTTACTTTTGC[C/G]CAGATTGATCAGAGG	54778
rs567985715	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59051867	CTACAGTGTTTTTTT[A/T]AAAGAATATATCACC	54778
rs568009125	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59012239	GGCCAGGCTGGTCTC[G/T]AACTTCTGACCTCAG	54778
rs568014371	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58989176	TGATAGTTTATTACT[A/G]TATGTATTTTTGTAA	54778
rs568016300	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:58995330	ATCTGATTAATACAG[A/G]ATTGTGTGTTTCCTG	54778
rs568033615	snp	C/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59067399	GATGGCTGGAAAACC[C/G]AGCATGAGGGAGTAA	54778
rs568045002	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59011817	GTGTTAGGACTTCAA[C/T]GTATGAATTTTGGGG	54778
rs568051134	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59018168	AATTATTATCATTTT[C/T]GAGCATTAAAATTTA	54778
rs568107225	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58994627	AGATTATAGGTGCCC[A/G]CCACCACGTCCAGCT	54778
rs568123746	in-del	-/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59068581	ACTGCACTCCAGCCT[-/G]GGCAACAGAGCAAGA	54778
rs568130504	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59079801	TCTTATTAAGGACTT[C/T]ACGTCCATATTTGAT	54778
rs568140459	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59017822	GAGTGCAATGGCACA[A/G]TCTCGGCTCTCTGCA	54778
rs568184458	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59079072	AATAGAGGAAGGGAA[A/T]GGGTTTTTGGGAATG	54778
rs568189683	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59092305	AAGTGAATGAATTTC[G/T]GTTAAATTTGATTTT	54778
rs568217629	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59000359	AGTAGAGACGGGTTT[C/T]ACCATGTTGTCCAGG	54778
rs568241817	snp	A/C	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59005455	ATTGTTTCCTTGGGC[A/C]GTTTTGCTCCCAACA	54778
rs568252375	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59006348	AAGTTCCTTTGTGCT[A/C]TTTTGCCATCAGCCA	54778
rs568262529	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59048383	CTTAACATAAAACTT[C/T]ACAAAATCCAAACCA	54778
rs568272190	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58992944	GAGGCTGAGGCAGGC[A/G]GATCACCTGAGGTCA	54778
rs568293583	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59057599	CTTAACTCACTCATA[A/C]GTTGAAGTCTACCTG	54778
rs568335077	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59091722	AATACCAACGGTCCC[C/T]AACCTTTTTGACACC	54778
rs568354607	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59054015	ATCTTGGCTCACCGC[A/T]GCCTCCATCTCCTGG	54778
rs568364857	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59084378	TAATCCCCAGTTTAA[C/G]TGAGACACTGCCTCT	54778
rs568386315	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59024132	AGAAGGAAATTGAGC[A/C]ATAGTAAATTTTCAA	54778
rs568438550	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59083671	CATTAAAATGGTTGA[A/G]TGTCTTTACAGTATA	54778
rs568516268	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF111	GRCh38.p7	15:58987425	AAATGAACCAAGATG[C/T]AGTCAAGATTTGGCT	54778
rs568523172	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58987879	TGGGCCGAGTCCAGG[C/T]GCTGCCGCACGTACA	54778
rs568524878	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:58990395	CCAGGCGTGGTGGCT[A/C]ACCCCTGTAATCCCA	54778
rs568588498	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59029422	TGAACTACAGATAGC[A/G]CGTGATGGCTGATCT	54778
rs568609425	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59071485	CGCAAGAGTTCGAGA[C/G]CACCCTGTGCAACAT	54778
rs568642571	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59059068	GGATCACTTGAGACC[A/G]GGAGTTCAAGACCAG	54778
rs568654586	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59035515	ATTTCATTCCACATA[A/G]CTTATGCAAATTTCT	54778
rs568750262	in-del	-/C	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:58992702	GCACATGCCTGTAGT[-/C]CCAGCTACTCGGGAG	54778
rs568776158	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59064024	GTAGCAAGTAAAGCT[A/G]CTGTAATAATGAGTA	54778
rs568789408	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59046969	GCCCCCTGGTTTCAA[G/T]TGATCCTACCACCTC	54778
rs568791105	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59028885	CCCAGGTTCAAGCGA[C/T]TCTCATGCTTCAGCC	54778
rs568807629	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59004626	TTTTGTTTCTTGTAA[A/C]AAGAATTTTCACTTC	54778
rs568853032	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59053474	TGATTTTAAAAGTAT[A/G]TATTCATATTTCTGA	54778
rs568855314	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59009876	CGGGAGGATCACTTG[A/C]GCCCAGGAAGTCAAG	54778
rs568859513	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF111	GRCh38.p7	15:59097402	AACAGTTGTGATAAA[C/T]TGATCGTTTGAAACG	54778
rs568923463	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	RNF111	GRCh38.p7	15:59097874	GACAGAGCCAGACTC[A/C]CTCTCAAAAAAAAAC	54778
rs568988149	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59039483	CTTTTGAGTATCATT[A/G]TGAATGCATGAATTT	54778
rs569008268	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59016378	TTTCACCATGTTGGC[C/T]AGGATGGTCTTGATC	54778
rs569015973	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59094523	TACCAAAACAAAACT[A/G]GAATAATTGGCAGTG	54778
rs569026631	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59043199	TCATTTTGTTGCCCA[C/G]GCTGGAGTGCAGTGG	54778
rs569061292	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59045051	ATTCATAAAAAGTTA[C/T]ATAAATTGAATTTTC	54778
rs569071267	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58991835	ATATGTTGGTGTTGT[C/T]TAAACCCTGACTCAA	54778
rs569078674	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB	RNF111	GRCh38.p7	15:58986466	TCATGATCCGCCCGC[C/T]TTGGCCTCCAAAAGT	54778
rs569093118	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59027977	ATTACAGGTGCACGC[C/T]ACCATGCCCGGATAA	54778
rs569142577	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59033703	GTGCCAGGGGTTCAT[A/G]TAGCCTCAAGTATTA	54778
rs569192386	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59019266	TTTAATTATTTTAAA[A/G]TTCCACTGAACAAAA	54778
rs569196011	snp	A/G	0.000296531	0.0121728	missense	RNF111	GRCh38.p7	15:59076119	CAACCTTTATCATCA[A/G]TAGATGGCTATGGAT	54778
rs569205051	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59014845	ACTGCAGTCCTTACC[G/T]CCTGGGCTCAAGCGA	54778
rs569210337	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59076677	CCAGCCTAGGCAACA[C/T]AGTGAGACCCCGTTT	54778
rs569225954	snp	C/T	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021534	TTATGTATGTACCTG[C/T]TCCTTTAGGAAAGTA	54778
rs569242397	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58991197	CCTGGCTGCTCAAGA[A/G]GGTAAGGCAGAATTG	54778
rs569245765	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020667	AAAATCATTAAGTTC[A/T]CTGAGAAATTGAAAC	54778
rs569278691	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58997600	GAGGTGGCCACATCA[C/T]GAGGTCAAGAGATCG	54778
rs569281705	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59034633	ACTTAGCTCTATTAT[C/T]AAGAAATCTCAGCTC	54778
rs569360267	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59008655	CCCAGTGTTGATACA[A/G]TTGGATTTAAATCTG	54778
rs569361444	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59065472	TTTTCTAACAACCAT[A/G]CAAGGCAATTTTATT	54778
rs569366834	snp	C/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:58997183	AGGCTCCTTGCCATT[C/G]TTATCTTCCTATGAC	54778
rs569368547	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59051418	AGCAGAGATGGCGCC[A/G]CTGCACTCCAGACTG	54778
rs569439722	snp	G/T	0.00199481	0.0315187	utr-variant-3-prime	RNF111	GRCh38.p7	15:59095364	TAGAAAATGATAATA[G/T]TGTGTATTAAGACAT	54778
rs569477494	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58996187	ACTGTTTATTAAAAA[C/G]CTGAAGTTTATACTT	54778
rs569483257	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:58989527	CTATATCATGTGCAG[A/C]TCCTTCTGTCACTTC	54778
rs569509846	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59087887	GCATTTGGCAGTAGA[A/G]TGGTTATTGGTCTTT	54778
rs569520675	snp	A/T	0.00478085	0.0486577	intron-variant	RNF111	GRCh38.p7	15:58995485	TTTTTTTTGACGGAG[A/T]CTCACTCTTGTCTCC	54778
rs569520723	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59001787	AATCATGTTTAAAGA[A/G]CTAAGTACAGTAGTC	54778
rs569575732	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59086753	AGCTGGTGTTTCTAA[G/T]TTTAGGAGTGAGGGT	54778
rs569637823	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59086364	CCTCAAGTGATCTGC[C/T]CACCTTGGCCTCCCA	54778
rs569657517	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59026673	TCCTTTTGAACTTTC[C/G]TCTTCTAAGTTCAAA	54778
rs569670400	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59069003	CGATTGAACGTGGGA[A/G]GCGGAGATTGCAGTG	54778
rs569699386	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59032331	GTTTCTTTAATATGC[G/T]TGACTGTTATGAATA	54778
rs569755696	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59029028	CCAGTGATCCGCCCG[C/T]CTTGGCCTCCCAAAG	54778
rs569791459	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59001733	ACAGAACACCTACAA[A/G]ACATACATTATCATG	54778
rs569828483	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59000016	TAATCCAGTCACCTC[C/T]AGGCAGGCCCCACCT	54778
rs569873563	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59073922	ACTGGATGTTGTGTT[A/G]GGTATGAAAACATTA	54778
rs569880459	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59007474	TTATCCATTCACTTG[A/G]AGATTTATTTTTTCT	54778
rs569897309	in-del	-/TAGAACGATACCAAAAT	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59009583	GGTGATTAGATAATA[-/TAGAACGATACCAAAAT]TAGAACGATACCAAA	54778
rs569920339	snp	C/T	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:59067280	CATTCTTCCTTCCTT[C/T]CCTCTCTTCCCCTCC	54778
rs569941645	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59043860	TGGTACCATGGTGTC[A/G]TTTATGAAAAGAATA	54778
rs569960263	in-del	-/T	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59014049	CCTTCCATGGCCTCC[-/T]CAACATGCTAGGATT	54778
rs569963719	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59055969	CAGGGAAATTGTCAG[A/G]TTTTTTAATCTCGTT	54778
rs569965546	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59013635	TTTGCCAGGTTTCTC[C/T]ACTATAAAGTTACTC	54778
rs570004843	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59043184	TTTTGAGACAGGGTC[G/T]CATTTTGTTGCCCAG	54778
rs570008044	snp	C/G			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022105	CCTAAAGTGATCTCC[C/G]CGCCTTGGCCGCCCA	54778
rs570015063	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59050091	TTGTTTTGAGATGAA[C/G]TCTCATTCTGTTGCC	54778
rs570078301	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59049480	TGCTTTTCTGGGTGG[A/G]GAATGCTGGTGCTTC	54778
rs570188226	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59042050	TTTTATATATTAGCA[A/G]TGTAAGTCCTATATA	54778
rs570195413	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59070334	TGTTTTTATTTTCCC[-/T]TTATTCTTTAATTTT	54778
rs570201782	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58989026	GGGAAAAACATAAGC[C/T]AAGGTTCCATTTCCT	54778
rs570202841	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59018718	TCCTATAATAGCAGA[C/T]TTACTTGTAGTCCGT	54778
rs570223995	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59061113	ATGTGTAGCATTATT[C/T]TTACGTACATTTTAT	54778
rs570230690	snp	C/T	0.00438332	0.0466095	intron-variant	RNF111	GRCh38.p7	15:58994455	ATGTTGTCACTCTTG[C/T]TTTCTTATTTTCTCT	54778
rs570251482	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59041576	AAAAGAAAAAAAAAA[A/T]TACTGCAATAAATAG	54778
rs570255364	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59087816	GTTCAAGGGTGAACT[A/G]TAATATGGTCAGTAT	54778
rs570263472	snp	C/T	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59047608	TGAGACAAGGTCTGG[C/T]TCTGTTGCCCAGGCT	54778
rs570266165	snp	A/T	0.00199481	0.0315187	utr-variant-3-prime	RNF111	GRCh38.p7	15:59095298	TTTTTATCCATTACT[A/T]ACCTTTAATTTAATC	54778
rs570281681	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59071934	TACATATAAAATTTA[A/C]TATTTACACTGTACT	54778
rs570302535	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59036916	CTCGCTGCAGCCTCA[A/G]CCTCCTTGGGCTCAG	54778
rs570313337	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58988437	GAGTTGGAGGGCGCT[A/G]AGTCAGCCCTGACGG	54778
rs570325834	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59024304	TTACTCATTCTTTTA[A/C]AGATTAATGCAATTA	54778
rs570330732	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59079621	CAAGAACATCTTCCA[A/G]TAAAATGAAATTTGT	54778
rs570389609	snp	C/G	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59036310	AGATCCGCTGCCCAC[C/G]TCAGCCTCCCAAAGT	54778
rs570405354	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59011619	AATGATCGCTTGCTG[G/T]GTTCTCACATAATCT	54778
rs570451622	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59023505	TTTGTGTAAAGGAAA[G/T]TCATTGATTTTTGGA	54778
rs570466978	snp	C/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59000322	GCATGTACCACCACA[C/G]TTGGCTCATTTTTCT	54778
rs570475944	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59084531	TGGAGGTACAGCATA[C/G]TATTTCAATACATAC	54778
rs570487095	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59084912	CAAAGTTGACTCCCT[C/T]GACTGATCTTACTTT	54778
rs570490622	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59029232	TTTATTACAGCCATC[C/G]TGTTTGGCCCCATTC	54778
rs570506321	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59054240	CCACGCCTGGCCTGG[C/T]CCTTTCATTTAAGAG	54778
rs570554939	snp	C/T	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:59006248	GAGGCACACGTTTTA[C/T]GTATAGTTGGATGAA	54778
rs570582271	snp	C/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59003844	GTGCCTAGCTCATTA[C/T]AGGCTTTCAATAAAT	54778
rs570643087	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59011627	CTTGCTGTGTTCTCA[C/T]ATAATCTTTTTTTCT	54778
rs570666787	in-del	-/A	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59009397	AGAACCCACTTTATT[-/A]CCATTGTGCTTTTTA	54778
rs570676718	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58998915	TGACCATGATGTTAC[A/G]AAGTCATGTCTGGGT	54778
rs570677466	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59017698	TACTTGAATTATCAA[G/T]AACAAAAGGTCCTGG	54778
rs570694414	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59090708	AGATAACTTTTGCTG[C/T]ACCATTTCAGTTGGC	54778
rs570694934	snp	C/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59017053	ACTGATTCTATATTA[C/T]GGTGAATTGTATAAT	54778
rs570713817	in-del	-/TT			intron-variant	RNF111	GRCh38.p7	15:59038255	TGCATCACTAGAAAC[-/TT]TGTCTCAAACTACAA	54778
rs570717167	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58987754	GAGCAGCGGCAGTGG[A/C]GGCGACGGCGAGGAG	54778
rs570745686	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59059231	TTCTGAAGAAGTTAT[A/G]CAAATGACCAAGAAG	54778
rs570749445	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59062488	TACATGATATCTTAT[A/G]TATTCATTTGTTTAA	54778
rs570768483	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59089948	GGGTCAAAAGTTACC[A/G]AAATATTTAAAGATG	54778
rs570865000	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59071993	GAAAAAATGTACATG[C/T]TTCAATTTAAAAATA	54778
rs570923159	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58991676	GCTACAGATAGCAGG[A/G]GCGGCAAATGCATTA	54778
rs570926563	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59071468	CGGGTGGATCGCTTG[A/G]CCGCAAGAGTTCGAG	54778
rs570975204	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59032278	TAGATTATATTTTAT[C/G]TATGTTCTTCATTTA	54778
rs571008596	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096715	GAGTGAAGGAGTCAG[C/T]GACCTATGTCTGCCA	54778
rs571014149	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59005038	CATGGTTTAAATTAT[G/T]TTTTTCTTGTCAAGT	54778
rs571080760	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59046937	CAATGGCACAGTCTC[A/G]GCTCACTGCAGACTC	54778
rs571113682	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59069933	ATGCAGTAGTCATGT[A/C]GATAGCCCTCACTGC	54778
rs571149249	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59009773	CAGACTGGGCAACAT[G/T]GCAAAACCTCGTCTC	54778
rs571173005	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59009415	ATTGTGCTTTTTACA[A/G]GTGACCAAATGGTGA	54778
rs571180229	snp	C/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59008046	TAAGAAATGGTAGTA[C/G]TTTCTGTATCCTGTG	54778
rs571198041	snp	C/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59046399	GGTTTCACCATGTTA[C/G]CCAGGCTGGTCTCGC	54778
rs571205107	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59015818	TCGTTTTGTTCCTAC[A/G]GAGTGCTTTTATTTA	54778
rs571235806	snp	A/C/G			utr-variant-3-prime	RNF111	GRCh38.p7	15:59095842	AGACACATTAAGTCA[A/C/G]GATTTGGAATTTAAG	54778
rs571261985	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59052786	AGCTATATTGTTGCC[C/T]AGACTCTTTCCCATA	54778
rs571278408	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59052160	GTTTTTTGTTCCTTG[C/T]GTATTTTTTTAAAAA	54778
rs571281839	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59058077	GTGATAGATCAGACA[A/G]CTTATTTAGAAGCTA	54778
rs571288368	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59075547	TATTTTCAGTAGTGT[A/G]ATAGTATGTTTTCTC	54778
rs571309041	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59091305	AAAGTATAAAAAATA[C/T]ATACTTTGCAGTTTT	54778
rs571329131	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59044667	CAGTCCTACCACTGT[C/G]TTAGCCATACTCGTT	54778
rs571404853	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021456	ATGCCTGGCCTATGC[A/C]CTTCTGGATCTCAAA	54778
rs571427652	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990696	TGTTGTTCCACATAT[G/T]ATTGCTATTGTTGTC	54778
rs571452458	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59033051	GTTGAAGTGAGCATT[A/G]AAGAGCTGTCTGAAC	54778
rs571494805	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58997530	TTAAAAAAAAAAAAA[A/G]AATCAGGGCTGGGTA	54778
rs571511693	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59041344	GTGGATCATGAGGTC[A/G]GGAATTCAAGACCAG	54778
rs571513733	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58997118	AAAAGTAATATATAC[A/T]AAGTGTACCAAATTT	54778
rs571549421	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59089188	TCACACATATGTAAT[A/C]CATAAATAATGAAGA	54778
rs571563905	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59039441	AATGACTTAGTTGTT[C/G]TAGCAGCATCCAAAG	54778
rs571582359	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58997556	GGGTATGGTGTCTCA[C/T]GCCTGTAATCCCAGC	54778
rs571606686	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59065880	GCCAGGCGTGGTGGT[C/G]TGTGCCTATGGTCCC	54778
rs571607247	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59068760	ATTTTGATGGTATGT[A/C]TTCTGGGTCTGACAG	54778
rs571692114	snp	A/G	3.33389e-05	0.00408269	missense	RNF111	GRCh38.p7	15:59055731	TGGAGCCAGGGTTCC[A/G]GTTCTCATGCAAGTC	54778
rs571703934	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59019670	ATTGGATATTTAAAA[A/G]TATTTAAGCCAGGCG	54778
rs571708654	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59070374	TTCTTCTAGGAATTA[C/T]TTTACTCTGGGAATG	54778
rs571733987	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59087171	TATGTTTTGATCTGT[C/T]AGTATATGGAGGTAA	54778
rs571740078	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59043729	AAAGTAGAGTCATTT[C/G]CTTATACCTTCAGTA	54778
rs571758693	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59056670	GGTGGTCATAACTTT[A/C]AGAGTATCAGTACCC	54778
rs571759369	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59008612	AAGTCTGTTTCTGGA[C/T]TCTCTAGTCTGTCCT	54778
rs571795964	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59008248	TGGAGACAAGAGTCT[G/T]TCTCTGTTGCCCAGG	54778
rs571803957	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59019869	GAGGCTGAGGCAGCA[A/G]AATTGCTTGAACCTG	54778
rs571810888	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59024425	CTTATATTCTACTGA[A/G]ACGCTTTGTGTAATA	54778
rs571810978	snp	C/T	0.000399281	0.0141238	synonymous-codon	RNF111	GRCh38.p7	15:59031089	ACAAGAAAAAAGTCT[C/T]GTTGTGAGGAAAAAA	54778
rs571819979	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59062269	GCTGGTCTCGAACTC[C/T]TGGACTCAGGCAATT	54778
rs571832042	snp	C/T	0.00636936	0.0560724	intron-variant	RNF111	GRCh38.p7	15:59053416	ATTTTTGTGTTGGAA[C/T]GAATTTAGAAGTGCA	54778
rs571879394	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59049828	TCTCGGCTCACTGCA[A/G]CCTTTGCCTCCCAGG	54778
rs571879638	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59074681	TTCTTTAGATCAGCA[A/G]TAAGGGTGTTTCAGT	54778
rs571909513	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59003352	TCAAGCCATCTGCCC[A/G]CCTTGACCTCCCAAA	54778
rs571926675	in-del	-/TTC	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:58996114	ACATAATGAGTTATG[-/TTC]TTAATTGTGATCATA	54778
rs571950109	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59019377	TTTAAAGGCCTGATA[C/T]GTCTGATGGTAATGT	54778
rs571950330	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59061164	TTTCAGAATATTCCA[A/G]AAACTTTTATATATA	54778
rs572014521	in-del	-/CTCTA			intron-variant	RNF111	GRCh38.p7	15:59061617	TCTCTACCTGTCCTC[-/CTCTA]CTAATTCCTAGTCTC	54778
rs572037241	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59006543	CAGAAAAGATGAAAG[A/C]ATTGTACAGTGAACG	54778
rs572070731	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59018484	AAAAATTTAAATATA[C/T]TATGTTCTCATAATT	54778
rs572072880	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59060622	CCCAGATGACAGAGT[A/G]AGACCCTGTTTTAAA	54778
rs572125328	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59005201	TAGTACATACTGTTT[A/G]TTTATTTGTCGAGAC	54778
rs572148336	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58994236	TAGAGATGGGGTTTC[A/G]CTATGTTGGCCAGGC	54778
rs572159084	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59011912	TCTTATGGTTCACTA[C/G]CAAACTAGGATTGTC	54778
rs572170570	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59036376	AAGACTGGTAACTTA[C/T]AAAGGAAAGAGGTTT	54778
rs572243515	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59011193	GTTCTTCGAATTTCA[C/G]TGTCTTATCCTTCCT	54778
rs572244507	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59027589	GCTGGAGTGCAATGG[C/T]GCAATCTCGGCTCAC	54778
rs572263660	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58995817	CTTTCTGGCACAGCA[A/G]GATGTTGCAAGCACA	54778
rs572270726	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59085151	GAACATAAAATGAGA[A/G]TAAGTAAATGAAGAC	54778
rs572272257	snp	G/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59092140	ATTCAAGTTTTCAAC[G/T]GTCCAAGTTAAATAC	54778
rs572285109	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59042221	AACCTCAGCCTCCCA[C/T]GCTTAAGCAATCCTC	54778
rs572312834	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59073033	AAAAATTAGCTGGGT[G/T]CAGTGGCACGCGCCT	54778
rs572318597	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59035986	TTTACAGAATCACCC[C/G]ACTCTGTTAGTACCA	54778
rs572380679	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF111	GRCh38.p7	15:58987528	ACTGATAAAACCAGT[A/G]CAAAGGGGGAGGGCC	54778
rs572388027	snp	A/G			utr-variant-3-prime	RNF111	GRCh38.p7	15:59096951	ACATCAGATTTAGAT[A/G]CACGACTACCTGTTG	54778
rs572423274	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59047370	CATGGTGGCAGGTAC[C/T]TGTAGTCGCAGCTAC	54778
rs572424834	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58998502	ATTGCATACCAAAGT[A/G]TGATGCTTATTTTGA	54778
rs572436166	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59084679	GTTATTCTTCACTGT[A/G]GTCACCATGCTGTGC	54778
rs572453494	snp	C/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:58995214	CTTGCCTATGCTGAT[C/G]TTTACTGATCTTTAC	54778
rs572457069	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59090378	GGGATTACAGGTGCC[C/T]GCCACCACGCCCGGC	54778
rs572468656	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	RNF111	GRCh38.p7	15:58986982	ATCTAACAAGAACCT[G/T]TTGAGGTAAATACGT	54778
rs572470392	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59048495	TTGCGAGCTCTTTTG[A/G]GGTTATTGGAAATGT	54778
rs572489329	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59017881	TCCTGCTTCAGCCTC[C/T]CGAGTAGCTGGGATT	54778
rs572497985	snp	C/T	1.65784e-05	0.00287905	synonymous-codon	RNF111	GRCh38.p7	15:59091148	ATATCCACATAAATA[C/T]AAAAAGGTAAGAATT	54778
rs572502807	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59056964	GGGTTAAAAGTATTC[A/C]AGTGATTAGTAGATG	54778
rs572505159	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58991905	TCTGAATATGGATGG[A/G]TATTAGATGATATCA	54778
rs572507167	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59043644	AATGCTACAGTGAAC[A/G]TTTGGGTACAAATCT	54778
rs572536892	snp	A/G/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59081940	TGAGATGAAAGGATC[A/G/T]TCTGAGCCCAGGGGG	54778
rs572537820	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59077908	CTTTTCCTGAAGGAG[C/T]GTGTGTATTCTCTCC	54778
rs572545798	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59054040	TCCTGGGTTCAAGCA[A/G]TCCTCCTCCCTCAGC	54778
rs572646209	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59059501	TGCACTAAGTCTACT[C/G]CTTAGTTATCTTCCC	54778
rs572655506	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59022644	AAGGAGTATAGTGAA[C/T]GTCTTTGGGTTTAGG	54778
rs572658392	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59065198	GGATGGCAGCAGGGC[A/G]GGGCTTTGGCTTTAG	54778
rs572661293	snp	G/T	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59053713	ACTCAATTTTTATGA[G/T]CTGTAAGGACTACTG	54778
rs572724856	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58992557	GCCCAGTGGCTCATG[C/T]CTGTAATCATAGCAC	54778
rs572771735	snp	A/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59040992	CTCTTTCATTTTTTT[A/T]CTTCAAAAATATACC	54778
rs572775474	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59058639	CTAAGATTTTAGCTA[C/T]GTTAATAAGCGGGTA	54778
rs572781058	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59028997	GTTGGCCAGGCTGAT[A/C/G]TCGAACTCCTGGCCT	54778
rs572826364	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58987775	CGGCGAGGAGGTGTT[C/T]GGTTTGCGCAGCGTA	54778
rs572866957	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59035188	CCCCATGAATTATGT[A/C]CACCTGGCCCTGTCC	54778
rs572868617	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59028187	CTAGGTAACCACATT[C/G]TATCTATGTAGATTT	54778
rs572878338	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58997941	GCTGAGTCTCACTCC[A/G]TTGCCCAGGCTGGAG	54778
rs572887851	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59058192	CACGTCTGTTCGATA[C/T]TGCAGTTTAGCTTTG	54778
rs572929014	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59040154	CGGTCTCACTCTGTT[G/T]CCTAGGCTGGAGAGC	54778
rs572955501	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59011974	AAGAATAAGTGGCTT[A/G]ATTTTAGTGTTCTTT	54778
rs572962815	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59046045	CTAATAAATGTTATG[C/T]TTTCTAATTGATAAT	54778
rs572969689	snp	G/T	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59027544	TTTTCTTTTTTTTTT[G/T]GGGAGACAGAGTCTT	54778
rs573008139	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59016450	ATTCTGTAATTCTTT[C/G]CATCATCCTAAATTG	54778
rs573025992	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59089534	GCTTAGTTGGAGTTA[C/T]GTATTCTTATTGAAG	54778
rs573049276	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59088864	TTCTCTCCATAAGGT[A/G]TATGACAGCCTTCTT	54778
rs573090451	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59010032	TGATTTTGTCATTCA[A/G]TTTATATGCAATTTT	54778
rs573126465	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59009515	TCTAAAGAAAAAGTC[G/T]TTAGAATTTGATAAT	54778
rs573161966	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59012518	ATTGACTATTAATGC[-/A]TGATTGCTGAACATT	54778
rs573181525	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096823	GAATACCCCGGGTCT[G/T]TGCCAAGGGACTGAA	54778
rs573215204	snp	G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59063394	ATTCATGCCTGCCTC[G/T]CGATAATCCTGCTAG	54778
rs573216374	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59016007	AGGTGCACCCCACCA[C/T]ACCTAGATAACTTTT	54778
rs573225363	snp	A/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021201	TGTTGCCCAGGATGG[A/T]GTGCAGTGATGCGAT	54778
rs573234236	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59064076	TATAGGAAACAGTTA[C/T]TTAATGTTGGGTTCA	54778
rs573235108	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59038792	TTAGTTCCGGCAGTA[C/G]TTTGTTGATGATACT	54778
rs573246786	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59058579	TGGGGGAGGGGAGAC[-/T]TTTTGTCATTACTTT	54778
rs573253219	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59015472	AACTACTCTTTGCCC[C/T]CATCACTGTAAGAGC	54778
rs573255937	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59009614	ATTAGAACTTGGAGC[A/G]TTTGTGAGTGAGTGT	54778
rs573279236	in-del	-/GTCC			intron-variant	RNF111	GRCh38.p7	15:59093259	TGAGAGGCTTTGGAG[-/GTCC]TAGAAAGTTATAATG	54778
rs573283601	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59055997	GTTTTTAATTGATAT[C/T]CTAGGCTTGTAAATT	54778
rs573307218	snp	A/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59076428	TCTTTAGTATAGCTG[A/T]AGAAATGTGAAAGTT	54778
rs573323591	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59008350	AGCCTCCTGAGTAGC[C/T]GAGACTGCAAGGACG	54778
rs573360355	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59014360	GAATCTGAGCACTAG[A/G]ACTTAGTGCCCTTTT	54778
rs573367322	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58998094	ATTTTTAGTAGAGAC[A/G]TGGTTTCACTATGTT	54778
rs573369977	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59036775	TACTCCAAGACCCAA[C/G]AGTTGTATATAATTA	54778
rs573383377	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59011125	ACTTCATCATTAATT[A/G]TATAGTTTATTCAGG	54778
rs573397413	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58997293	GTCTGTTGACTCTTG[A/C]GGTAGCTCTTCCAAG	54778
rs573457373	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:58996736	GTTTCTCACCTGTGT[A/G]TGGATATTTGCTTTA	54778
rs573479348	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59002617	GTCATTTAGATCCAG[C/G]CTTTGCTATCAGGTC	54778
rs573487012	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59087983	AGGAAGTGAAAACAT[A/G]GAGACAGTGAATATA	54778
rs573493737	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59002186	GTGGTTAAGGGGAGA[C/T]TACTGTATAGTGTTG	54778
rs573508545	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59075669	CAAAAAGATTTTAAT[A/G]TATTAAACTTTTGTT	54778
rs573552046	snp	A/G	0.00478085	0.0486577	intron-variant	RNF111	GRCh38.p7	15:59044220	ATTATTAATAGAGAC[A/G]GGGTTTTGCCATGTT	54778
rs573561522	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59071025	AGAAGTGGCCGGGCG[C/T]GGTGGCTCACGCCTG	54778
rs573565454	snp	A/C	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59059427	ATGCAAAATGGTGCA[A/C]CTGCTGAGAAAAACA	54778
rs573572918	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59074963	AGGGAGGCCCAAAGA[A/G]AGGAGAGCAGGGTAA	54778
rs573623512	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59078715	AATTCAAAAACTAGC[C/T]GGGTGTGGTGGCAGG	54778
rs573653762	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59050386	CCTTTGTGTTTGTCA[C/T]CTTGGTGAATTATTG	54778
rs573671528	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58989529	ATATCATGTGCAGAT[C/T]CTTCTGTCACTTCTT	54778
rs573688288	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59093907	GTATTGACAATACTG[A/T]TCAAGGAATAATTGG	54778
rs573725334	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59020141	TACATATTTTATATA[A/T]GTTAGATATATAAAA	54778
rs573734230	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59019658	AAACATGTTATTATT[A/G]GATATTTAAAAGTAT	54778
rs573776001	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59024189	TTTGTTATTATTATT[C/T]TCATTCTGCATATTT	54778
rs573808682	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59022849	GTCTAGGTTTTACTT[C/T]GGATCTGAGAAAAGT	54778
rs573811432	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59068018	TAGTATTGGCAATCA[C/G]GTGGAGTAAAAGAAG	54778
rs573821609	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59025856	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC	54778
rs573863264	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59085295	TAGCAAACAAAAACC[C/T]AGAGAGCATCTGTAA	54778
rs573865356	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59066132	TGTAGTGGAAGGACT[C/T]GTATTTTTAAACTTT	54778
rs573867611	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59062428	AATGTGCCACAAACA[C/G]CTCATTATCTGTCTG	54778
rs573872594	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59074097	CTCAACAGTATTCTT[A/C]AAATATTCAGTAAAC	54778
rs573885078	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59025245	TAACTTTCTCCTTTC[C/T]ACTAGGAAAGGTAAT	54778
rs573897641	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59067571	TTTCTTTTTAATTAA[C/G]TCTCTGGGATTTTTA	54778
rs573904706	snp	C/G/T	3.00919e-05	0.0038788	intron-variant	RNF111	GRCh38.p7	15:59055656	CTTTATTTATATTTA[C/G/T]TAACTTAATATTGAT	54778
rs573926010	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59061823	GTGTATTTTTGTCAC[A/G]CTAAACTCTTTCCTC	54778
rs573965352	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59054829	CTGTAAATGCTGACA[A/G]TAAGGTTATAAGCAG	54778
rs573989822	snp	A/G	0.00279162	0.0372561	intron-variant	RNF111	GRCh38.p7	15:59032003	GAGTGCAGTGGCGCA[A/G]TCTCGGCTCACTGCA	54778
rs574013274	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59073570	TTTACGGCAATTCAA[C/T]CACATCTTCAGGTTC	54778
rs574028005	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59041501	GAGGTTGCAGTGAGC[C/T]GAGATCTAGAGATTG	54778
rs574082296	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59042818	AACACTCTTTTAATT[A/T]TAAAATCTTTAATGT	54778
rs574086553	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59007065	TGCTGGAATTCCAGG[C/T]TGTTTACAGTTTTTA	54778
rs574126871	snp	A/G			utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096364	TATGTGAAGATGTCA[A/G]TAAGCTTGCATTAAG	54778
rs574143920	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59059939	TTTAATTCTTTTAAT[A/T]TTCATGTAATTTACA	54778
rs574200189	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59006643	CTATTTGTTCCTCCA[A/G]CCGTCCATCAACCAA	54778
rs574222076	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:58997518	ACACATTTGCAGTTA[-/A]AAAAAAAAAAAAAAT	54778
rs574232278	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59058114	AAACTGTTAAATCAC[C/G]TAAATTATTGGAATA	54778
rs574260993	snp	A/G	0.00438332	0.0466095	intron-variant	RNF111	GRCh38.p7	15:59027906	TCTCAGCTCACTACA[A/G]CCTCTGCCTCCCTGG	54778
rs574287632	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59035896	CCCACATCTTCTTAT[C/T]TTTGGAGCTCTCCAA	54778
rs574290685	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59025985	TCTGCCTGCCTTAGC[C/T]GCCCAAAGTGCTGGG	54778
rs574304980	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59013272	GCTCACTCAGTTACC[C/G]TTGTTGTTAACATCT	54778
rs574310004	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59041671	AGTTGTTGAATAAAG[A/G]ATAAATGCATATGTT	54778
rs574323915	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59035331	AATCATGCCTTCCCA[A/C]CAGTCCCCCAAAGTC	54778
rs574332977	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59024393	TCTGCCTAGATGAGA[G/T]TCCTGCTTCCTTGGA	54778
rs574419206	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59030445	TGAATTCGAATCCTT[C/T]TATTTATATTTCACT	54778
rs574420774	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59030070	CTCTTTTTGGCAGCT[C/T]GTAATTTAAGATGTT	54778
rs574422971	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59041164	TTGTTAAGCTTCATC[A/G]TACTCCCTTGCATGG	54778
rs574480666	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58990409	TCACCCCTGTAATCC[C/T]AGCACTTTGGGAGGC	54778
rs574483369	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59029831	GTGTTCATTTTTTTA[C/G]TGTTCATTCATCTAT	54778
rs574552481	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59013132	TAGTCACTCATTTCT[C/G]TCCTGCCTTTCCTAG	54778
rs574555334	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58999750	CTGAGACTGGGTAAT[A/T]TATAAAGAAAAGGGG	54778
rs574579442	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59077847	TAGGAAATTTAAATT[A/G]TATTATTTTCTGTTA	54778
rs574633462	in-del	-/TTC	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:58996078	CATAAAGCAATTTTT[-/TTC]TTCTTTTCTTTTTCA	54778
rs574637792	snp	G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59016592	AACATTTTTCATCTT[G/T]CTCGGCCCACCATAA	54778
rs574639432	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59005759	TGGACGTCTTTGCCT[A/G]GACGATTTCTAAAAA	54778
rs574743037	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59090346	GCAATTCTCCTGCCT[C/T]GGCTTCCTGAGTAGC	54778
rs574755336	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59073248	GAGAGGCTGAGGCAG[G/T]CAGATCACTTGCGGT	54778
rs574771614	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59047298	CTCAGGAATTCGAGA[C/G]CAGCCTGAGCAACAT	54778
rs574774396	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59084641	TTTAAAATCTTTTGT[C/T]GCAGTTTTGAAATAA	54778
rs574862335	snp	A/G	0.0134861	0.0810011	intron-variant	RNF111	GRCh38.p7	15:58998444	AGTGTTCTTCCCCTC[A/G]TTGTGTCCGTATGTT	54778
rs574877826	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RNF111	GRCh38.p7	15:59097632	CGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCTGA	54778
rs574902814	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58997807	GCGACAGTGTGAGAC[C/T]CCATCTCAAAAAAAA	54778
rs574930201	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59083220	AACTGACTTTAGGAA[A/G]AGAAAATACAGTAAA	54778
rs574989552	in-del	-/GG	0.0105946	0.0720075	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:58988080	TAAGGTGAGGGGAAC[-/GG]GGGGGGAGGGGATCC	54778
rs574993779	snp	A/C/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59082725	CTGAAAAAATTTCCC[A/C/G]TTTTACCCTTCACAT	54778
rs574996224	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59088784	CAACTTTAAAAAATA[C/T]TGTAGAATCATTAAC	54778
rs575010601	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	RNF111	GRCh38.p7	15:58985882	AAAGGGGAGGGGAGA[A/G]GGAGAAGAGGAGGGA	54778
rs575037286	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59070942	TCAGATCTTTATGAT[A/C]TTTCATCACATTTTG	54778
rs575055394	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59070301	AACTGGAATTGTGAA[C/G]AAGAGGGTTCTCATT	54778
rs575070424	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59058864	AATTTAGAACTTTCG[C/T]GCATTAAAGGATATT	54778
rs575070777	snp	C/T	0.00398564	0.0444627	intron-variant	RNF111	GRCh38.p7	15:59065158	GATTCTGAGGAGATG[C/T]CTCAGAATCAGAGTA	54778
rs575116195	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59003802	TTTCTATGTCCTGTT[C/T]GTGGCTGATGCCAGT	54778
rs575133743	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59064672	AAGTTCACAGACGCG[C/T]GAATTCTAGTTCCCA	54778
rs575146050	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59086720	AGCAAATAGCACAAG[C/T]ACTGGGAACTCCAAG	54778
rs575155289	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59017083	TATTATATATTGCAA[C/T]GCAATGATAATAGAA	54778
rs575166609	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59076552	TTTTTATATTCATTT[C/G]ATGCAGGCAATTAAA	54778
rs575171546	snp	A/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59027228	CATAAAGACTCCAAG[A/G]TCTCCTCCTCTGAAA	54778
rs575180181	in-del	-/TTTG			intron-variant	RNF111	GRCh38.p7	15:59018419	CTTGCATATATTTGA[-/TTTG]TTTGTGTAGAAATCT	54778
rs575219173	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59034373	TGTTACCAGAATGCC[C/T]TCCAAGAAGTTTGCA	54778
rs575276227	snp	C/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59039868	ACTACAGGCACATGC[C/T]ACCGTGCCCAGCTAA	54778
rs575283025	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59062702	AGGCAGATTTTATTA[C/T]TCTTCTCATTCTACA	54778
rs575292277	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59003524	CCACCTCAGCCTCTC[C/T]AGTAGCTGGGACTAC	54778
rs575295066	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59068688	ACCGTGCCCGGCCAA[A/G]CTACCACTTTTCTAT	54778
rs575329751	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59039672	GGTGCAGATTAATCT[A/G]CAGTTCCTGCCCCAG	54778
rs575354095	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59051738	GATCATCCCACTGCA[C/T]TCCAGCCTGGGCAAC	54778
rs575361060	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096750	ACTGGGGAAAAGAGC[A/G]AGTAGCCTGTCTTCC	54778
rs575368394	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59008951	TAATATTGTCACGTA[A/T]TTTATTTTATTTTAT	54778
rs575387324	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59052218	TTTGCAATGAATTTC[A/C]TGGTCTTCAAAGTCA	54778
rs575388256	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59038581	TATAATCATCATCTC[A/G]CTTCAGTTGTTGACA	54778
rs575449400	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59037920	CTCCTAAATAAGAGA[G/T]CTTAAGTCAGTCCCA	54778
rs575502160	snp	A/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59045412	GCCAGGCTGGTCTCG[A/T]TCTCCTGACCTTGTG	54778
rs575532865	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59015875	ATTTATTTATTTATT[C/G]GAGACAGGTTCTCAC	54778
rs575566201	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58993110	AGGAGGCAGAGGTTG[C/T]AGTGAGCCAAGATTG	54778
rs575571777	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59006584	TGCCACCTAGATTCT[A/G]TGATTAACAATTTGC	54778
rs575581058	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59026917	ACACCAAACCACCCC[C/G]CCTTGCTCTCCTCTA	54778
rs575601385	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990737	TATTAATTACTGAAG[C/T]TTTAATAGCTTTCAG	54778
rs575631309	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990460	AGGTGACCAGTCTGG[C/T]CAAAATGGTGAAACC	54778
rs575644729	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59075614	AAGGAGAATATAGAA[G/T]TATGATTTTTAAAGT	54778
rs575672214	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59074934	AATTTCAATGTTGTT[A/G]TGTCTCAGGGAATAG	54778
rs575677735	in-del	-/AG	0.0126979	0.078662	intron-variant	RNF111	GRCh38.p7	15:59037026	TTTTTTGGTAGAGAC[-/AG]GGTTTTGTCATGTTG	54778
rs575725441	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59080626	GCATATACACAGATA[C/T]TTATCATAGCATTTG	54778
rs575764399	in-del	-/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59040301	TAAATTATATTTTAA[-/T]TTTTTTTTTAGAGAT	54778
rs575840034	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59038821	CTGTGTGCTTTCTGT[G/T]GCGTCACAAATTGAG	54778
rs575887536	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59059107	ACATGGTGAAACCCT[A/C]TCTCTATTTATATTT	54778
rs575890475	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59008284	GTGCAGTGGCACAGT[A/C]GTGGATCACTGCAGC	54778
rs575923945	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59050924	ATCAAAAATTAATGG[A/G]GTAAAAAAGATTTTT	54778
rs575925041	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58994725	TTAAGTGATCAGCCT[A/G]CTTCAGCCTCCCAAA	54778
rs575941362	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59050323	AAGGAACAACTCCAT[A/G]TTTTCCAAAAGCCCT	54778
rs575954070	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59056178	AAGCAGTACTTTTTA[A/G]ATATAAACACAAAAG	54778
rs575959902	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59000888	TAAGCTTTTGGGCAC[A/G]TAGTAGTGATCAAAA	54778
rs575961918	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:58994289	AGTAATCCTCCCGCC[C/T]TGGCCTCCCAAAGTG	54778
rs575980035	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58998351	TTTCACCACCCAGGT[A/G]TTAAGCCTAGTACCT	54778
rs576009936	snp	A/T	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59086603	GTTGTGGGTAGAGGC[A/T]CTGCAGGAAAGCTTT	54778
rs576049664	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59013374	ATTTCATTGTAGACT[A/C]TGGTTTCACAGTTTC	54778
rs576064974	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59085876	CTATATTAATATAGA[C/T]GTTTTAATAGAATTT	54778
rs576070535	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59093767	TGCCCTAATTTATAA[A/G]GATAACTTTGTCGTA	54778
rs576070915	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59024838	ACTCCTATTCTCCCC[C/T]TCCCTCAGGTCCTCG	54778
rs576163112	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58989506	TCTCCTTGTTTATCA[C/T]GGGTGCTATATCATG	54778
rs576164535	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59043572	AGTGAGCAGGCTCCT[A/G]TAGGTAGGTAGAGGT	54778
rs576169959	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59076584	TATAACCATGGTTGG[G/T]CATGATGGCTCACTC	54778
rs576170669	snp	G/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59061695	CCTCTTATCCTTTCC[G/T]TTGTCCTTAACCTTG	54778
rs576193401	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59018480	AGTGAAAAATTTAAA[A/T]ATATTATGTTCTCAT	54778
rs576230235	snp	A/G	4.94295e-05	0.00497115	synonymous-codon	RNF111	GRCh38.p7	15:59031287	TGATACTGTGACTTC[A/G]GATGAGGATAAAGAA	54778
rs576233344	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59000790	ACTATTCTCCTTTCA[A/T]CCCATCTTTCAGTTA	54778
rs576249454	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59040256	GAGTACTTGGGACTA[C/G]AGCACATGCCATCTT	54778
rs576272808	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59079939	GCTTCCATATATGCA[A/C]ATAATACTTACAAGT	54778
rs576279892	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58988779	ATTTAATTTGTTCGT[C/G]TGTGTGTTGTGGGGT	54778
rs576280127	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59067978	TATTATTATTGAGTT[C/T]GCAAAATGTCAACTA	54778
rs576295703	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59072575	TCTGCCTCAGCCTCC[C/G]AAGTAGCTGGGACTA	54778
rs576297767	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59037277	GGTTATTAGAAAGCC[C/T]GTTAAACATTTAGTT	54778
rs576299961	snp	C/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59073081	GGAGGCTGAAGTTGG[C/G]AGGATTGCTTGAGCT	54778
rs576338882	snp	A/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59036552	CTTGTTCACTACCGT[A/G]AGAACATGGTATGTG	54778
rs576344807	snp	A/C	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59067500	AGGGATAGATTTTAT[A/C]CACTAAATTAATCAC	54778
rs576353845	snp	C/T			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020236	TAAAGATAATATGTA[C/T]ATACTGTACATAAAT	54778
rs576356190	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59093542	ACTGGTTTTGTCATA[A/C]AATTTCCTCTAAACT	54778
rs576406504	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59066133	GTAGTGGAAGGACTC[A/G]TATTTTTAAACTTTT	54778
rs576409812	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59079225	ATTTGTGAATGTTGT[A/G]TAATGATTACACAAA	54778
rs576457252	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59042739	TAAATTTTCCACATG[C/T]ATTTGGGCCTGTTTA	54778
rs576520230	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59042327	GGATGAGGTTTTGCC[A/C/G]TGTTGCCCAGGCTGG	54778
rs576525371	in-del	-/TCT			intron-variant	RNF111	GRCh38.p7	15:59044339	CCTGGCCATGGAAAC[-/TCT]TCTTATTGTTAGCAT	54778
rs576549331	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59054759	TGACCTTTGGAGTTC[C/T]CTTCTTAGTGGTTAA	54778
rs576566577	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59060324	AAAAAAAAAAAATCC[G/T]TGACATGGTGAGACT	54778
rs576579217	in-del	-/T	0.0236746	0.106192	intron-variant	RNF111	GRCh38.p7	15:59042126	TACTTTTATGCCAAA[-/T]TTTTTTTTCTTTTTT	54778
rs576585227	snp	C/G	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:59054066	TCAGCCTTGTGAGTA[C/G]CTGGGATTACAGGCA	54778
rs576636095	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59048888	TTGAGCCTAGGAGTT[C/T]GAGACCAGCCTGGGC	54778
rs576639061	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59059883	TTAATAATGAAACCA[C/T]CTTATATTTTCTATC	54778
rs576688273	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59018301	CGGTCACTGCCATTT[C/T]TGAGTTTCTGCCCTA	54778
rs576702814	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59047885	CAGCCTACTTATTTT[A/G]GAAATGGTTATTAAA	54778
rs576743366	in-del	-/AGA	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59070626	ATTGTACAGCTCAAC[-/AGA]AGGAGAACAGACATA	54778
rs576766963	snp	C/T	0.00199481	0.0315187	intron-variant	RNF111	GRCh38.p7	15:58993126	AGTGAGCCAAGATTG[C/T]GCCACTGCCCTTCAG	54778
rs576817212	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59078355	ATTATTTAAAAGTTT[C/T]ACTATCTTATTAATA	54778
rs576846004	snp	A/G/T	0.00438476	0.0466401	intron-variant	RNF111	GRCh38.p7	15:59029023	GGCCTCCAGTGATCC[A/G/T]CCCGCCTTGGCCTCC	54778
rs576856456	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59023785	CACTATTAACCATCA[A/G]TTTTTTTCCCCCTGA	54778
rs576882738	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59035223	CACGTGGGAATTATT[A/G]TAAGTCAAGGTGAGA	54778
rs576886239	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59077972	GTATGCTTTAGTTCA[C/T]GTGTGAAACATGTGG	54778
rs576892661	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022436	TAGACAGACCTCCCA[A/G]AAGATAACTTTGACT	54778
rs576908392	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59047866	AGGCGTGAGCCACTG[C/T]ATCCAGCCTACTTAT	54778
rs576933490	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59033327	TTTTCTCTTTTTGCC[A/G]GAACCCTAAACCAGT	54778
rs576949095	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59044133	CCTCCCGGGTTCAAG[C/T]GATTCTCCTGCCTCA	54778
rs577004143	snp	A/G	0.000154486	0.00878745	intron-variant	RNF111	GRCh38.p7	15:59084083	GAAAAGAAATAACCA[A/G]TTATTCAATTATTTC	54778
rs577011114	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59027585	CCAGGCTGGAGTGCA[A/G]TGGCGCAATCTCGGC	54778
rs577018291	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59010995	CCTTTTCTCCCTAAC[A/G]GTCATCGTTCTAGAC	54778
rs577040740	snp	A/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:58999173	TTTAACCAGAACAGC[A/G]TATCATGATAAATGG	54778
rs577051793	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59083404	TTAGCTGGGCGTGGT[A/G]GCATGCACCTGTAGT	54778
rs577088704	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59053624	TTATTTTCCCCAACT[C/T]TGAGTAAAACTGAAA	54778
rs577109155	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59010104	TGCCCTCACATGAAA[A/T]CATGGCTAAAAACAG	54778
rs577156607	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59053142	AAAACATATGTTTTG[A/C]TTCTTTTTCCTTCAC	54778
rs577170637	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59058835	GCAAAAGTAGATAAG[C/T]TGGACTTCATCAAAA	54778
rs577205090	in-del	-/G	0.0493028	0.149066	intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:58988081	AAGGTGAGGGGAACG[-/G]GGGGGGAGGGGATCC	54778
rs577230651	snp	A/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59058270	GTTTTTTTATTTATT[A/T]ATTATAAACACATTA	54778
rs577232286	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59016047	GTAGAGACAGGGTTT[G/T]GCCATGTTTTGACCT	54778
rs577251596	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RNF111	GRCh38.p7	15:58986671	AGGCGTCCGCCACCA[C/T]GCCCAGCTAGTTTTT	54778
rs577264020	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59030690	GTGTACTGATGAGGA[A/G]AAGACAGTTCTGCCT	54778
rs577322576	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59075551	TTCAGTAGTGTGATA[A/G]TATGTTTTCTCAAGG	54778
rs577328492	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF111	GRCh38.p7	15:59095918	GGATCACTTTTAAGG[A/G]ATTTTTATTAGTTTA	54778
rs577347127	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59064127	TGATCATGGTCAGTT[C/T]CTGATATGCTAGTTT	54778
rs577389441	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59094684	AGGAAGATGCTTAGT[A/G]CCTTCAAAACATTAT	54778
rs577393366	snp	A/G	0.00159617	0.0282053	intron-variant	RNF111	GRCh38.p7	15:59033827	GTTATTTTTAACTAC[A/G]TTATTTTCAGACACT	54778
rs577459144	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990951	CAGGTTTCTACAGGT[A/G]CTCAATTTATATCAT	54778
rs577479533	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59033387	TGTTCAGATCAGTTT[C/T]ACCTACACAAATACT	54778
rs577482375	snp	C/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59082550	CAGCAAACTATTGGT[C/T]TAATTCTGCCTACTG	54778
rs577485340	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	RNF111	GRCh38.p7	15:58985709	GATTTAACCCAATAT[A/T]TCCAAAATATTATTT	54778
rs577497214	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58997406	TGACATTTGCACTGA[C/T]GGTGCAAAAAACAGT	54778
rs577517649	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59039197	TCGAACTCCTAACCT[C/T]AGGTCATCTGCCCGC	54778
rs577555246	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59070205	TGCATCATTTATAAT[C/T]TGTGTAAGCCAATTA	54778
rs577659285	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59068047	AGTCAAGCGTTCCAT[A/G]CTACTTTAACTTTTG	54778
rs577662683	snp	A/T	0.0023933	0.0345097	intron-variant	RNF111	GRCh38.p7	15:59045831	TGCATTGTGTTTATG[A/T]TTATGAAGCAAGAGT	54778
rs577666250	snp	C/G			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020560	ATTGAACTTCACCCA[C/G]TTTGTATTGACAGGA	54778
rs577706368	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59015050	CTGACCACTGTGCCT[C/T]GCCACCCAATTTCTT	54778
rs577722235	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59092161	AGTTAAATACTGTAA[C/T]TAATGTTAATTTAAA	54778
rs577756378	snp	G/T	0.00318978	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59080554	TTATGCTACAGAAAT[G/T]ATCTCTATATATGTG	54778
rs577764524	snp	C/G	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59056904	AAGGTGATAGAGTAG[C/G]CTTTTCCACATTACA	54778
rs577773136	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59063224	CATTGTGCAAGCATG[C/T]TTCTGGTTGCTAGAG	54778
rs577779568	snp	A/G	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59062609	CTCTAGTGGATAGCA[A/G]TAGCTAACATTTATT	54778
rs577827455	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59062627	GCTAACATTTATTGA[G/T]CCTATAGTGTTGGCC	54778
rs577839357	snp	G/T	0.00119737	0.0244387	intron-variant	RNF111	GRCh38.p7	15:59051667	CCAGCTACTTGAGAG[G/T]CTGAGGCATGAGAAT	54778
rs577889673	snp	G/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59056112	GTTAGCTCAAACTAG[G/T]TTAGTTTGATTTGTA	54778
rs577889977	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59049768	TTTTTTTTTTTTTGA[C/G]ATGGGGTCTCGCTCC	54778
rs577955561	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59063618	TTATTTGGGTAGTAA[C/T]TCTCGAATGAGAGGC	54778
rs577960484	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58990203	TAAATGAGAATTGTA[A/G]AATAGATAACTTTCG	54778
rs577972141	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:58996338	AGCACTTCGGGAGGC[C/T]GAGGCATATGGATCC	54778
rs577989246	snp	C/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59038436	GATCAGGAATTATAT[C/G]TAATGCTGTGAATAC	54778
rs578041923	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59015275	GAAGGCTTTCTTTGC[A/G]TACTAGCATGTTAGA	54778
rs578046795	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59080370	AGGTGACTCTGCCCA[C/T]CTTGGCCTCCTAAAG	54778
rs578061708	snp	C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59032543	CCTCCCACGTCAGCG[C/T]CTCAAGTAGCTGGGA	54778
rs578063824	snp	C/T	0.00358779	0.0422022	intron-variant	RNF111	GRCh38.p7	15:59037834	AGAGTGAAACTCCCT[C/T]TCAAAAAAAAAAGTA	54778
rs578082516	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59065926	TGAGGCAGGAGAATC[C/T]GTTGAGCAAATATAT	54778
rs578089482	snp	A/C	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59032063	CCTGCGTCAGCCTCC[A/C]AAGTAGCCAGGATTA	54778
rs578091513	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59061209	CACAAATCAGATTTA[A/C]TTTCTGAGCATCTTG	54778
rs578109686	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59043413	CTGCCTGCCTTGGCC[C/T]TGCAAAGTGCTGGGC	54778
rs578132490	snp	A/G	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:58992197	TTACAGGAGCGCGCC[A/G]CCACGCCTGCTAACT	54778
rs578133195	snp	G/T	0.00517822	0.0506191	intron-variant	RNF111	GRCh38.p7	15:59043020	GAATATGGGATGTCT[G/T]CATTTGTTGATGTCT	54778
rs578162369	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59001487	AGGGAGATTTGAAAT[A/G]AAGGTCTTGTATAAC	54778
rs578164814	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096556	CATTCAGTTATGACT[A/G]CTTGCCCTTTTCTTC	54778
rs578193851	snp	C/T	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59086041	AAGATACTCTTAATC[C/T]ACTGTCAGGAGTATA	54778
rs578226307	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59001111	ATGTAAAGGAAGTGA[A/G]TGAGTGAGCCTCGTG	54778
rs578248968	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59093684	CCTGTTCTTTTTTTT[A/G]ATGTTAACATAATGC	54778
rs578252161	snp	A/G	0.000399281	0.0141238	intron-variant	RNF111	GRCh38.p7	15:59093009	CCTGTCTCTGAAAAA[A/G]AAGAGTAAAAGTAAA	54778
rs745325518	in-del	-/C	1.64886e-05	0.00287124	frameshift-variant	RNF111	GRCh38.p7	15:59085702	GCAGCTACTTATACA[-/C]CTGGTGCATTGCATC	54778
rs745346859	snp	C/G			intron-variant, missense	RNF111	GRCh38.p7	15:59022551	GAATGGAGGATGTCC[C/G]TTAATCTCCTCACAT	54778
rs745379757	snp	C/G	3.47252e-05	0.0041667	synonymous-codon	RNF111	GRCh38.p7	15:59080940	TTTTCTTGCAGATGC[C/G]TCTTTGACAAGGCCA	54778
rs745397913	snp	C/T	1.6473e-05	0.00286988	missense	RNF111	GRCh38.p7	15:59058464	CCTCTGATACTGCTT[C/T]AGCTGTCACCAGTAG	54778
rs745449066	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58999682	AAGCATTTATGAGTT[C/T]TACTTTCTAATAGGG	54778
rs745468254	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59046404	CACCATGTTACCCAG[A/G]CTGGTCTCGCACTCC	54778
rs745480118	snp	G/T	3.31505e-05	0.00407113	intron-variant	RNF111	GRCh38.p7	15:59058564	AGGTATGTAAAAAAG[G/T]GGGGGAGGGGAGACT	54778
rs745483170	snp	A/G	1.65018e-05	0.00287239	synonymous-codon	RNF111	GRCh38.p7	15:59031401	GACAGAATCTGTATC[A/G]GGATTGTTAATGAAA	54778
rs745507263	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59005992	TGCCTGAGCAAAGAA[C/T]TCCAAAATTTAGGAA	54778
rs745516157	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58995897	CCCTGGTTCCTTTTA[A/G]TGAGCAATCCAATTT	54778
rs745523183	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58994961	CAGTTTTGTCGAATT[A/G]TCCTGATAATAGCAT	54778
rs745555178	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59074593	TTGAAGAGTTAGGGC[C/T]TTGCTCTGGCTTAGG	54778
rs745567058	snp	A/G	1.6517e-05	0.00287372	missense	RNF111	GRCh38.p7	15:59031493	ATAATTCCTCACAGA[A/G]GACACAGAAACAAAA	54778
rs745576587	snp	A/T	1.70353e-05	0.00291846	intron-variant	RNF111	GRCh38.p7	15:59084283	TTAATTTCAAAACAG[A/T]GCTTCACAGCTTGTG	54778
rs745586252	in-del	-/TTTG			intron-variant	RNF111	GRCh38.p7	15:59090212	TGGTTTGTTTTTTTG[-/TTTG]TTTGTTTGTTTGTTT	54778
rs745603584	snp	A/C/T			intron-variant	RNF111	GRCh38.p7	15:59085533	ATTTTGGGCTAAATT[A/C/T]TCTTTCCTCAGCTTT	54778
rs745632933	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59043423	TGGCCTTGCAAAGTG[C/T]TGGGCTTGCAGGTGT	54778
rs745636918	snp	A/G	0.000117105	0.00765106	intron-variant	RNF111	GRCh38.p7	15:59052268	ACGATTAGCTGACAG[A/G]AAGATGCCTTTAAAT	54778
rs745677896	snp	A/G	1.6528e-05	0.00287467	intron-variant	RNF111	GRCh38.p7	15:59089796	TATGTTTGTCACAGT[A/G]TCTTTAATGCAGATT	54778
rs745682654	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59044496	TTTATAAAGAACTCT[C/T]GCAGAGAAACCATTG	54778
rs745693767	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59086375	CTGCCCACCTTGGCC[C/T]CCCAAAGTGCTGGGA	54778
rs745695254	snp	G/T			upstream-variant-2KB	RNF111	GRCh38.p7	15:58987281	ACAGTGAGGTGCCGT[G/T]ATCTTTATGTCATTA	54778
rs745703368	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59016892	CAGCGGCATTCTTGT[A/G]GGAGCATGAACCCTA	54778
rs745789551	in-del	-/TATT			intron-variant	RNF111	GRCh38.p7	15:59089952	CAAAAGTTACCGAAA[-/TATT]TAAAGATGAGTAAAT	54778
rs745792578	snp	A/G	9.90001e-05	0.00703493	missense	RNF111	GRCh38.p7	15:59091099	TAGGCAATGTCAATC[A/G]TGGAGCATCCCAGGG	54778
rs745812172	snp	A/G			utr-variant-3-prime	RNF111	GRCh38.p7	15:59097088	GGAGCTTATTAAGCT[A/G]CTGCCATTAGTTATC	54778
rs745819875	snp	A/G/T	3.40033e-05	0.00412319	missense, stop-gained	RNF111	GRCh38.p7	15:59030850	ACTCCTGAATATAAC[A/G/T]AGCTCTACACCTTAA	54778
rs745827922	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59015695	GTTGCCATTTCTTAG[C/T]ATTGTTTGAAGTGAA	54778
rs745834732	in-del	-/TCTT			intron-variant	RNF111	GRCh38.p7	15:59041043	TTACTCAAAAGTGTC[-/TCTT]GCTTTTTTCACTTAA	54778
rs745837134	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59056690	TATCAGTACCCAGTT[A/G]TTTATGAAGAGATAA	54778
rs745883130	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59089228	ACTAACAAAAAATTA[C/G]AAAACAGTGTTAAAA	54778
rs745888751	snp	C/G	0.000132807	0.00814774	intron-variant	RNF111	GRCh38.p7	15:59076231	GTAAGTATATACTTA[C/G]TGGACACAAAATCTA	54778
rs745914517	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59054588	ACCACAACTGTTTCT[A/G]ATATGTACTATCCTA	54778
rs745923008	snp	C/G	3.29701e-05	0.00406005	missense	RNF111	GRCh38.p7	15:59031045	GATTCTCAAAAGCAA[C/G]AGAAGGAAATGAATG	54778
rs745943624	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59048006	ACCTTCATTTCCCTA[C/T]TGGGAATGTAAAATT	54778
rs745969875	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59035281	TCATTCTGCCCCTGC[C/T]GCTTCCAAATCCCAT	54778
rs745993161	in-del	-/ATAT			intron-variant	RNF111	GRCh38.p7	15:59015356	TTCTTATGAATTCAC[-/ATAT]AGTTTTACAATAGTA	54778
rs745995144	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59008347	CTCAGCCTCCTGAGT[A/G]GCTGAGACTGCAAGG	54778
rs746035390	snp	C/T	1.6476e-05	0.00287014	missense	RNF111	GRCh38.p7	15:59031148	ATGTGCAGAATTGTG[C/T]TAAAGAAAACCAGGG	54778
rs746041511	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59029932	TGTTTTGCACTAGTA[A/G]AGCTCTTCATTTGTC	54778
rs746041603	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58993160	GGGTGACAGAGCAAG[A/G]TTCCATCTCAAAAAA	54778
rs746082498	snp	A/C	1.64735e-05	0.00286993	synonymous-codon	RNF111	GRCh38.p7	15:59081141	AGCCAGTACAGCTGC[A/C]CCAATCCCTCAGCAT	54778
rs746087808	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58992347	ACCGTGCCCAGCAAT[A/G]TCTGTTATTTTAAAC	54778
rs746145886	snp	A/C	0.00011532	0.00759255	synonymous-codon	RNF111	GRCh38.p7	15:59081204	TATTCCAGCCACAGC[A/C]CCTCCAGCACAGAGA	54778
rs746152005	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59082777	ATCTAATTAATGATC[C/T]AGCTCTCTTGTGTAA	54778
rs746155694	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59087964	TCTTAGATTACGTAC[A/G]GTAAGGAAGTGAAAA	54778
rs746163782	snp	C/G	1.71167e-05	0.00292542	intron-variant	RNF111	GRCh38.p7	15:59066756	TGTGCATTTTTTTCT[C/G]TTTCAAGATGACTCA	54778
rs746209290	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59040888	AAAAAATTTAATTTC[A/G]CTTTTTAAATTATGT	54778
rs746242177	snp	A/G	3.29745e-05	0.00406031	synonymous-codon	RNF111	GRCh38.p7	15:59085710	TTATACACCTGGTGC[A/G]TTGCATCCTCACTTG	54778
rs746249351	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59059201	TTTAAAATGAGAAAA[C/G]ATTTGAATAGATATT	54778
rs746255606	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59003218	CCTCCTGGGCTCAAG[C/G]GATCCTCCCACCTCA	54778
rs746276820	in-del	-/A			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986952	TTCAGAGCATTATAT[-/A]AATTGTCTCATTTAA	54778
rs746308182	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59075580	GGAGTCCTAAAGTAC[-/T]AGTCACAATGTTGGG	54778
rs746403093	snp	A/T	1.71994e-05	0.00293248	missense	RNF111	GRCh38.p7	15:59055709	CCTTGGACACTCCAG[A/T]TCTCATTGGAGCCAG	54778
rs746413826	snp	G/T	1.64792e-05	0.00287042	missense	RNF111	GRCh38.p7	15:59076020	GGCAGTTTTCATGGA[G/T]CATCTGCATTTGACC	54778
rs746442972	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59081858	ATAAGGAGACCTCGT[C/T]TCCACCAAAAAAAGG	54778
rs746464277	in-del	-/C			intron-variant	RNF111	GRCh38.p7	15:59074792	GTGCAAGAGGCCTAG[-/C]CTTTTGGCCTCTCTG	54778
rs746482801	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59032491	TAGTGATGCAGTCTT[C/G]GTTCACTGCAACCTT	54778
rs746504764	snp	A/C/G	4.95285e-05	0.00497616	missense	RNF111	GRCh38.p7	15:59031505	AGAGGACACAGAAAC[A/C/G]AAAAGAGAGGATATT	54778
rs746552067	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58994862	AAATATTCACTGTGT[A/G]TTGTATTCTTTTGCG	54778
rs746568544	snp	A/G			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021411	CTGTCTCGGCCTCCC[A/G]AAGTGTTGGGATTAT	54778
rs746593408	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59015454	ATGTGGTGAAACTGC[C/T]AAAACTACTCTTTGC	54778
rs746606068	in-del	-/CTTTTTTT			intron-variant	RNF111	GRCh38.p7	15:59017753	ATTATTTGTTGAACT[-/CTTTTTTT]TTTTTTTTTTTTTTG	54778
rs746627377	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59043314	TACCTACCACCTCAG[C/T]CAGCTGATTTTTTTA	54778
rs746638884	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59084442	AGCTGGGGCAGGGAA[A/C]CATATCAAGCAGGAG	54778
rs746658636	in-del	-/C			intron-variant	RNF111	GRCh38.p7	15:59002288	CCACTTGAAATTTTA[-/C]TTTTAAAGATCAACT	54778
rs746706383	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58993948	TCAATGTTGTAGTCA[C/T]TTCCCTTATTCATAT	54778
rs746712759	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59005785	AAAAACTAGCTGACT[C/T]GTCATCTTTAAAACA	54778
rs746722498	snp	C/T	3.33367e-05	0.00408255	intron-variant	RNF111	GRCh38.p7	15:59075942	GATAAAATATACTTC[C/T]TTTTTATCTAGCAGG	54778
rs746740966	snp	A/G/T	5.23495e-05	0.0051159	intron-variant	RNF111	GRCh38.p7	15:59085798	ATGGTAAAATGGAAA[A/G/T]TTTTCAAAATTTTGA	54778
rs746767240	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59025956	GCTGGTCTCGAACTC[C/T]CAACCTCAGGTGATC	54778
rs746772802	snp	C/T	1.68462e-05	0.00290221	synonymous-codon	RNF111	GRCh38.p7	15:59030858	ATATAACGAGCTCTA[C/T]ACCTTAAAAGTGGAT	54778
rs746782888	snp	C/T	1.66283e-05	0.00288338	intron-variant	RNF111	GRCh38.p7	15:59076238	TATACTTAGTGGACA[C/T]AAAATCTAGAGTCAT	54778
rs746802331	snp	G/T			utr-variant-3-prime	RNF111	GRCh38.p7	15:59095930	AGGGATTTTTATTAG[G/T]TTAAAGGTAAATAAA	54778
rs746806319	snp	C/G	1.89831e-05	0.00308078	missense	RNF111	GRCh38.p7	15:59092543	TTCTCACAGAGGAAA[C/G]TGCACTGCAAACAAG	54778
rs746810954	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59067942	TGTCAGCAAAAAATT[A/C]TAATTAAGTAAATTA	54778
rs746855550	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59073789	TCTGGAAGGTTTTCA[A/G]TTTACTTTTGCCCAG	54778
rs746859065	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59048528	TTAAACTGGATTGTG[G/T]TGATGATTACACTCC	54778
rs746862245	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59037001	ACTACAGTTGACTAA[-/T]TTTTTTTTTTTTTTT	54778
rs746868868	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59036625	CCCTTGGCATGTGGG[C/T]ATTATTACAATTCAA	54778
rs746893754	snp	A/C	1.68193e-05	0.00289989	missense	RNF111	GRCh38.p7	15:59080963	CAAGGCCACTTCATC[A/C]TCAAGCTTCTGCCTG	54778
rs746900828	snp	A/T	1.6486e-05	0.00287102	synonymous-codon	RNF111	GRCh38.p7	15:59031017	GGGGAATGAATTCTC[A/T]CACCTGTGTGATGAT	54778
rs746926080	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58989099	TGAATGTGATTTTGA[A/G]ATTACCATACACAAC	54778
rs746955942	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59000407	GGCACCCGGCCCATT[G/T]TTAAGATTATGAAGG	54778
rs746968972	snp	A/G	1.65652e-05	0.0028779	missense	RNF111	GRCh38.p7	15:59066787	AGGAGAACTACATCT[A/G]GTGCTGTAACGGAAA	54778
rs746992011	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59079111	GTCACTCTTAAAATG[A/G]TCAGCAACCTGTTTT	54778
rs747003196	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58989530	TATCATGTGCAGATC[C/T]TTCTGTCACTTCTTA	54778
rs747007408	snp	A/G	1.65455e-05	0.00287619	intron-variant	RNF111	GRCh38.p7	15:59058566	GTATGTAAAAAAGTG[A/G]GGGAGGGGAGACTTT	54778
rs747068126	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59033895	AACCAAGTACATTCA[A/G]TGTTTTCTGGTTTCT	54778
rs747075522	snp	C/T			utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096339	GTGGAGGACATGTTC[C/T]CATGGATCATATGTG	54778
rs747092769	snp	A/G	1.64887e-05	0.00287125	synonymous-codon	RNF111	GRCh38.p7	15:59081246	TGAAGTGATGCAGAG[A/G]ATGGAAGTTCAAAGG	54778
rs747100788	snp	C/G	4.9423e-05	0.00497082	utr-variant-3-prime	RNF111	GRCh38.p7	15:59094946	TCATTCCCATCCTTC[C/G]TGGTACTGCAGTCAA	54778
rs747105568	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59059051	GAGGGGTTGAGGGTG[A/G]AGGATCACTTGAGAC	54778
rs747151813	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59017861	TTCCTGGGTTCAAAC[A/G]ATTCTCCTGCTTCAG	54778
rs747182708	snp	A/G	0.000118747	0.00770451	intron-variant	RNF111	GRCh38.p7	15:59084061	TAGGGATTTTTTTCT[A/G]CATTAAGAAAAGAAA	54778
rs747185983	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58990882	ACATTTGAATGTCTT[A/G]TACCTCTGTTTGTTT	54778
rs747203520	snp	A/G	3.29457e-05	0.00405854	missense	RNF111	GRCh38.p7	15:59066878	GGTCGTCACAGAACC[A/G]CCATGCATTAGGACA	54778
rs747230986	snp	C/G	6.58946e-05	0.0057396	missense	RNF111	GRCh38.p7	15:59066985	GCTGTCCCAGTTTCT[C/G]CTTCCTTTAGTGATC	54778
rs747239375	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:58991391	ATTTATTGAATGTCT[C/G]ATGTTCTAGGCACAG	54778
rs747274815	in-del	-/GTG			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986203	TGTGTGTGTGTGTGT[-/GTG]TTTTGTTTGTTTGTT	54778
rs747293833	snp	A/C	1.67739e-05	0.00289597	missense	RNF111	GRCh38.p7	15:59031697	ACAATCCAGCTGTTC[A/C]CTCAGGTAAAAATGT	54778
rs747311378	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59080677	GGATTTTGTCAGTAC[A/C]TTTTGGTGTGTTCAT	54778
rs747318696	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59052112	TGCAAAGAAGTGTAG[A/G]TTAAAACAGTGATTA	54778
rs747364628	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59092293	GTAATAGCTTTTAAG[G/T]GAATGAATTTCTGTT	54778
rs747380045	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59011882	ACTTGGCATATGTTC[C/T]AACTGAAGATAATGT	54778
rs747388455	snp	C/T	1.64789e-05	0.0028704	synonymous-codon	RNF111	GRCh38.p7	15:59076037	ATCTGCATTTGACCC[C/T]TGCTGCCCTGTTTCT	54778
rs747401511	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59081707	TAGGTGGTAGAGCAA[C/G]ACCCTGTGTCCTTTA	54778
rs747405844	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59080451	TTGATGGAAATATTA[A/G]TTATGGCAACCTTTT	54778
rs747423142	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:58995272	TAACTCATCCATTTT[C/G]TTCACTAATGGACAT	54778
rs747479681	snp	A/G	0.000318016	0.0126058	intron-variant	RNF111	GRCh38.p7	15:59093511	CCACTGCACTCGGCT[A/G]TAGCATCTTTTATAA	54778
rs747518713	snp	A/G	0.000164742	0.00907435	missense	RNF111	GRCh38.p7	15:59031160	GTGTTAAAGAAAACC[A/G]GGGAATATTAGGACT	54778
rs747524416	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59091792	GTGGCAGAGGGGATA[C/G]TTTCAGAATGAAACT	54778
rs747554425	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59063732	GCAAAAGAGGACAAG[C/T]TGTTTCTGAACAGAT	54778
rs747577535	snp	C/G	1.64757e-05	0.00287012	missense	RNF111	GRCh38.p7	15:59094814	CACCTTTTCCACCAA[C/G]TGTGTGTTGACCAAT	54778
rs747578365	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59039210	CTCAGGTCATCTGCC[C/T]GCCTTGGCCTCCCAA	54778
rs747583391	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59010873	ACAGTAGATTCCTTC[C/T]CCTGTTATTTAATTG	54778
rs747597261	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59084330	AGATGCCTTGTGATT[A/G]ATTGCTTTGCAGAAG	54778
rs747598745	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59042191	GTGCAGCATATTGCT[A/G]CCTCGGCTCATTGCA	54778
rs747617319	snp	A/C			missense	RNF111	GRCh38.p7	15:59030843	TCAATGGACTCCTGA[A/C]TATAACGAGCTCTAC	54778
rs747641266	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59056281	ATCCTTCAATATTAT[C/T]GGTACCTTTTTGTGC	54778
rs747650040	in-del	-/TT			intron-variant	RNF111	GRCh38.p7	15:58994475	TTATTTTCTCTCTCT[-/TT]TTTTTTTTTTTTTTT	54778
rs747700438	snp	A/G			intron-variant, utr-variant-5-prime	RNF111	GRCh38.p7	15:59004033	AAGTTTGAGTGACCT[A/G]TCCTGTGTTTATCCT	54778
rs747702151	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59025901	ACGCCTGGCTAACTT[C/T]GCATTTTTGGTGGAG	54778
rs747707812	snp	A/G			intron-variant, utr-variant-5-prime	RNF111	GRCh38.p7	15:59004020	CTTGGGATGGAAGAA[A/G]TTTGAGTGACCTATC	54778
rs747750433	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59041110	TAGAGGAATGAAAGT[A/G]TATATCTCCGTATAT	54778
rs747750704	snp	A/G	3.29783e-05	0.00406055	missense	RNF111	GRCh38.p7	15:59089752	GTCCTTTCAGGGGCA[A/G]TTTTGAGGTATGTAA	54778
rs747765927	snp	C/T			utr-variant-3-prime	RNF111	GRCh38.p7	15:59095574	GATAAGAGTTGAATA[C/T]TGATATCATACATTT	54778
rs747792526	snp	C/G	1.66012e-05	0.00288103	missense	RNF111	GRCh38.p7	15:59055803	ATACAGCCCTTGAGG[C/G]AGAATGCAGCAGAAG	54778
rs747799136	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58988868	AGAATTCTCTTGAAT[A/G]GTAAGATGCCAGCTG	54778
rs747830909	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59003415	CGGCCTTTTTCTTTT[C/T]TGAGACAGAGTCTGG	54778
rs747831945	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59049745	CTTTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTTT	54778
rs747870456	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59083010	GAATCTTAGCTGGGT[A/G]TGGTGGCACACACCT	54778
rs747873243	snp	A/C	1.64738e-05	0.00286995	missense	RNF111	GRCh38.p7	15:59076108	CTGCCCCAAGTCAAC[A/C]TTTATCATCAATAGA	54778
rs747951878	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59087087	ATGTACTGAATCTCT[A/G]TGAAAGTTGAATGTC	54778
rs747957830	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59066680	ACATTTCTTTAAACA[A/T]TTATTATTTATACCC	54778
rs747962828	snp	C/T	8.23662e-05	0.00641688	missense	RNF111	GRCh38.p7	15:59081109	CATCCTGTGGCACCC[C/T]CACCACCAACTCACT	54778
rs747968811	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59007041	TCTGCCTGCCTCAGC[A/C]TCTTGAAGTGCTGGA	54778
rs748024780	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:58999106	AAAGGTTATTAAATA[A/T]ACTACTCCCTTTTTC	54778
rs748050997	snp	A/G	1.77241e-05	0.00297686	intron-variant	RNF111	GRCh38.p7	15:59066728	ACAGTGATATTTCAT[A/G]ATTTGATTATTCTGT	54778
rs748056992	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59047124	CATCATGCCTGGCCA[A/G]GAATTCTTATAATTC	54778
rs748061003	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59034299	ATGTAAGTGTATCTT[A/C]AGGAATAATTACTGA	54778
rs748066106	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:58990721	GTTGTCCCATTGTAG[A/C]TATTAATTACTGAAG	54778
rs748066877	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58998344	CAGATTATTTCACCA[C/T]CCAGGTATTAAGCCT	54778
rs748087329	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59076388	GAGGTGGATTGAATG[C/G]AAGTTTTAAGGAATT	54778
rs748159731	snp	C/T	1.64999e-05	0.00287222	synonymous-codon	RNF111	GRCh38.p7	15:59031587	ACCTAGTTCTAGTAG[C/T]TCCAGTGAGAATGAC	54778
rs748205265	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59039036	ATGACACGATCTCAG[C/T]TCACCGCAACCTCTG	54778
rs748213895	in-del	-/TTT			intron-variant	RNF111	GRCh38.p7	15:58994474	CTTATTTTCTCTCTC[-/TTT]TTTTTTTTTTTTTTT	54778
rs748240011	snp	A/C	1.64735e-05	0.00286993	synonymous-codon	RNF111	GRCh38.p7	15:59066990	CCCAGTTTCTCCTTC[A/C]TTTAGTGATCCTGCT	54778
rs748253008	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59057910	TTATATTCATACTGT[C/G]AGTGGTGAAATCAGT	54778
rs748255569	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59070857	CAAATGCATTACCCT[A/G]GGTTTTTTCATCTCC	54778
rs748258704	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59000619	GGAGGCTGAGGCACG[A/G]GAATTGCTTGAACTG	54778
rs748308789	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:58990728	CATTGTAGATATTAA[G/T]TACTGAAGCTTTAAT	54778
rs748325879	snp	A/G	1.64974e-05	0.00287201	missense	RNF111	GRCh38.p7	15:59052305	TCTTTTTGTTTCCAG[A/G]AAGTATTGATGAAGA	54778
rs748327805	snp	A/C/G	3.31847e-05	0.00407326	missense	RNF111	GRCh38.p7	15:59067073	GTTCTGGTACCAGCT[A/C/G]TCATGAACAGGTATG	54778
rs748329480	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59015849	TAGCATGTTTATAAC[A/G]TATTCTGGTTATTTA	54778
rs748330020	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59037900	AAACGTAAATGTCAA[A/G]TATGCTCCTAAATAA	54778
rs748335641	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59036132	GGCTGCTGGAGTGCA[G/T]TGGTGTGATCTTGGC	54778
rs748443145	snp	A/G	1.65397e-05	0.00287569	synonymous-codon	RNF111	GRCh38.p7	15:59091133	AATTGAAAGATGTAC[A/G]TATCCACATAAATAC	54778
rs748443632	snp	A/G			utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096678	CCTTATGATTAAACC[A/G]AGGTTATAGAAGGTC	54778
rs748449227	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59062789	AGTCTGGCGTGGTAC[C/T]TCTACTTTTCCCCTT	54778
rs748462854	in-del	-/TGGAGATTC	1.64754e-05	0.00287009	cds-indel	RNF111	GRCh38.p7	15:59031263	ATCTAGTCTGCATTT[-/TGGAGATTC]TGATACTGTGACTTC	54778
rs748493988	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59079485	TAACAAGGCATACTT[C/T]GAAAATATAGTTGAG	54778
rs748496456	snp	A/G			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021212	ATGGAGTGCAGTGAT[A/G]CGATCTCGGCTCACT	54778
rs748497454	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59090421	TTTTAGTAGAGATAG[C/T]GTTTTGCCATGTTGG	54778
rs748533690	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59048419	TAATGACAGAGAGCA[A/G]ATCAGTTGTTGCAGG	54778
rs748548827	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59091741	CTTTTTGACACCAGG[G/T]ACCAGTTTTCATGGA	54778
rs748560607	snp	G/T	1.66996e-05	0.00288956	intron-variant	RNF111	GRCh38.p7	15:59058319	CCCTTTATCTAATTT[G/T]TTTTGAAATGCTAAG	54778
rs748578994	snp	A/G	3.29506e-05	0.00405884	missense	RNF111	GRCh38.p7	15:59094858	TAAGAAGTGCCCCAT[A/G]TGCAGAGTGGACATT	54778
rs748582171	snp	C/T			intron-variant, utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022279	TTGAGGTCTTTGTAC[C/T]TAGAGGCGACAGAGA	54778
rs748584309	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59009728	GAGAAGTTGAGGCAG[A/G]TAGATCACTTGAAGC	54778
rs748597781	snp	A/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022290	GTACTTAGAGGCGAC[A/G]GAGAATTTTACTTCA	54778
rs748609211	in-del	-/CT			intron-variant	RNF111	GRCh38.p7	15:59044338	GCCTGGCCATGGAAA[-/CT]CTTCTTATTGTTAGC	54778
rs748625153	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59080643	TATCATAGCATTTGG[G/T]TTTCTTTTTTATCAG	54778
rs748629352	snp	A/T	1.64789e-05	0.0028704	missense	RNF111	GRCh38.p7	15:59031316	AAGTCTCTGTAAGAC[A/T]TTCCCAGACCATTTT	54778
rs748640578	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58993768	GGAGAGTTTGGCAGT[A/G]TGGATTGTGTTAACA	54778
rs748645492	in-del	-/AA			intron-variant	RNF111	GRCh38.p7	15:59053879	TCTCTTATTGTTATT[-/AA]AAGAGATATTAATTT	54778
rs748669590	snp	A/G	5.12072e-05	0.00505974	intron-variant	RNF111	GRCh38.p7	15:59084075	TACATTAAGAAAAGA[A/G]ATAACCAATTATTCA	54778
rs748688120	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59082015	GAACTCCTGTGCTTA[A/T]GTGATCCTCCCATGA	54778
rs748729209	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59065718	AAGGAAGGAAAAAAG[-/A]ATAATGGCCCAGACA	54778
rs748735364	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59053673	ACCTATCCTCTGACC[A/G]TGCATAGTGCTTGGT	54778
rs748737478	in-del	-/TTTTTT			intron-variant	RNF111	GRCh38.p7	15:59008971	TTTTATTTTATTTTA[-/TTTTTT]TGAGACAGAGTCCCA	54778
rs748749575	snp	A/G	4.94931e-05	0.00497434	synonymous-codon	RNF111	GRCh38.p7	15:59091082	TCATTTGGAAGAAAG[A/G]TTAGGCAATGTCAAT	54778
rs748792932	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59093989	GTATAAAAACTCTTA[A/G]CAGTTGCTAGAAGTA	54778
rs748801990	snp	A/G	1.64817e-05	0.00287064	missense	RNF111	GRCh38.p7	15:59076138	ATGGCTATGGATCAA[A/G]CATGGTTGCGCAGCC	54778
rs748803144	snp	G/T	2.33528e-05	0.00341699	intron-variant	RNF111	GRCh38.p7	15:59030778	ACACATTAAAAATCT[G/T]TTAAATATCTAATTT	54778
rs748821264	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59078907	AGGTAAGGCTACTTA[C/T]GATTAATCATAAAGC	54778
rs748836548	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59054891	TTGTGTTTTATTGGC[C/T]TCACCTTTCTAAAAG	54778
rs748847524	snp	G/T	1.65924e-05	0.00288027	intron-variant	RNF111	GRCh38.p7	15:59058334	GTTTTGAAATGCTAA[G/T]TTGACATTTTGTATT	54778
rs748857311	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59013105	TGAAGTTAGAGAGCA[A/G]GGTAAGCTCCATAGT	54778
rs748863536	snp	A/G			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020340	TTTATGTCTTATTTA[A/G]TATACATTTCAGGAT	54778
rs748900024	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59041256	TTTTAAATAGCACTG[C/G]AATAAATAGCTTTTC	54778
rs748932093	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58997988	TGGCTCACTGTAATC[C/T]CTGCCTCCCAGGTTG	54778
rs748933440	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59065812	TGGAAGGAGCTTAAG[A/G]CCAGCCTGGGCAATG	54778
rs748952538	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59092752	TAATTCCAGCACTTT[C/T]TGAGGCCAAGGCCAG	54778
rs749012975	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59033331	CTCTTTTTGCCAGAA[C/T]CCTAAACCAGTAACC	54778
rs749014080	snp	C/G	1.64738e-05	0.00286995	synonymous-codon	RNF111	GRCh38.p7	15:59058438	TTCAAATCCATCTAC[C/G]TCTGAGCAGGCCTCT	54778
rs749018589	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59087578	ATGATAGTTTACAAT[A/C]AAGTAGAAAAAAATG	54778
rs749054033	snp	A/G	3.29484e-05	0.00405871	synonymous-codon	RNF111	GRCh38.p7	15:59066855	TCCCCAGCACTCACC[A/G]TGTGGAGGGTCGTCA	54778
rs749070728	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59045664	ATATGACTTGTCGTT[G/T]ATACATAATGCTTTT	54778
rs749095524	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59066565	GGTGAGCCAAGATGG[C/T]GCCACTGCACTCCAG	54778
rs749126481	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59017005	CCCCCAGTTGGGACC[A/G]TCTAGTTGCAGGAGA	54778
rs749137209	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59006878	TGCAACCTCCGCCTC[C/T]CGGGTTCAAGCAGTT	54778
rs749160152	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59006949	CGCTACCACGCCCAG[C/T]TAATTTTTTTGTATT	54778
rs749173855	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59034204	TCCCTTTGTATGGAT[A/G]TTCCATAATTTATTT	54778
rs749198183	snp	A/G	1.66763e-05	0.00288753	missense	RNF111	GRCh38.p7	15:59031685	AAAACCACCAAAACA[A/G]TCCAGCTGTTCCCTC	54778
rs749199985	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59044657	AAATCACCCACAGTC[C/T]TACCACTGTCTTAGC	54778
rs749200084	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59058881	CATTAAAGGATATTA[C/T]CAAGACAGTGAAAGA	54778
rs749217514	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59006145	CTTAATTTCTCTTTG[C/G]TTTTTCTGTGTATTC	54778
rs749266302	in-del	-/TTACTA			intron-variant	RNF111	GRCh38.p7	15:58988574	AAGAAACTGATGTTT[-/TTACTA]TTACTATTGTCCTTC	54778
rs749283326	snp	A/T	1.64988e-05	0.00287213	intron-variant	RNF111	GRCh38.p7	15:59089763	GGCAATTTTGAGGTA[A/T]GTAATAAAATAAATG	54778
rs749288212	snp	C/T	3.35081e-05	0.00409304	intron-variant	RNF111	GRCh38.p7	15:59052265	CTAACGATTAGCTGA[C/T]AGGAAGATGCCTTTA	54778
rs749344397	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59074181	GGCAGAATAGATTTA[C/G]CATAAATCTTAAGGG	54778
rs749362963	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59036730	ATGGAAAAATGTTTT[A/G]CATTTTAAGTATTTT	54778
rs749387272	snp	A/G	1.69591e-05	0.00291191	intron-variant	RNF111	GRCh38.p7	15:59052443	ATCGGTGAGATTTTA[A/G]TTCTTAGTTAAATGT	54778
rs749392400	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59037841	AACTCCCTCTCAAAA[A/C]AAAAAGTAGGTATTA	54778
rs749399993	snp	C/T	1.71507e-05	0.00292832	intron-variant	RNF111	GRCh38.p7	15:59075919	AATATTTGACCAAAC[C/T]TTAGAAAGATAAAAT	54778
rs749400348	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59008467	AAGCAATCCTCCTGC[A/G]TCAGCCTCCCAAAGT	54778
rs749404805	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59068012	TTAAATTAGTATTGG[C/T]AATCACGTGGAGTAA	54778
rs749439262	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59089336	ACTTATCTTGAAGTC[A/G]AATTTTGTTGGAAAA	54778
rs749447204	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59026026	TGAGCCACTGTGCCC[A/G]GCCGGCTTTTTTTTT	54778
rs749452163	snp	C/T			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021073	CCTGACCTCACTTTC[C/T]ACCCTTTCCCCCAAA	54778
rs749504258	snp	A/G	3.66542e-05	0.00428086	missense	RNF111	GRCh38.p7	15:59092558	CTGCACTGCAAACAA[A/G]ATGGGGAAGAAGGGA	54778
rs749538889	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59090275	TGCTCTGTCACCCAG[A/G]CTGGAGTGCAGTTGC	54778
rs749564812	snp	C/T	1.64855e-05	0.00287097	missense	RNF111	GRCh38.p7	15:59031024	GAATTCTCTCACCTG[C/T]GTGATGATTCTCAAA	54778
rs749588779	snp	A/G	1.65652e-05	0.0028779	synonymous-codon	RNF111	GRCh38.p7	15:59080982	AGCTTCTGCCTGCCC[A/G]CATTCTCATGGAAAC	54778
rs749651003	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59060364	AATCCCAGCTCTTTG[A/G]GAGGCCAGGGACGCA	54778
rs749652270	snp	C/G	1.6498e-05	0.00287206	missense	RNF111	GRCh38.p7	15:59031396	ACTGAGACAGAATCT[C/G]TATCGGGATTGTTAA	54778
rs749695120	snp	C/G	5.91011e-05	0.00543572	intron-variant	RNF111	GRCh38.p7	15:59084089	AAATAACCAATTATT[C/G]AATTATTTCCAGTGG	54778
rs749752050	in-del	-/CCCCCT	1.64836e-05	0.0028708	cds-indel	RNF111	GRCh38.p7	15:59076163	CAGCCCCAGCCCCAG[-/CCCCCT]CCCCCTCCACAGCCC	54778
rs749761930	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59041823	GTTTTTGGTCCGTCT[G/T]ATAGCTGAGAAATAG	54778
rs749811676	in-del	-/AGA	4.97088e-05	0.00498517	cds-indel	RNF111	GRCh38.p7	15:59031641	CTCATCAACTGAAGG[-/AGA]AGAAGATTTGTTTGT	54778
rs749819673	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59003884	ATGAGAACCATAAAT[C/G]AATAAGTGATAGCTA	54778
rs749828359	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58992638	GGCTGGGCAATGTGA[C/T]GAAATTCTGGCTGTA	54778
rs749850780	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59071443	ATCCTAGCACCTTGG[A/G]AGGCTGAGACGGGTG	54778
rs749919129	snp	A/G/T	4.94599e-05	0.00497272	missense	RNF111	GRCh38.p7	15:59031008	TAGTAAAGTGGGGAA[A/G/T]GAATTCTCTCACCTG	54778
rs749932339	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59088746	AGTGTATAACCTTTT[G/T]TATGTGTGTTTCTGC	54778
rs749966517	snp	A/G	1.66021e-05	0.0028811	intron-variant	RNF111	GRCh38.p7	15:59092685	TTGTCAAAACTGTAC[A/G]TGGGATTTTATTTGA	54778
rs749967535	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59050267	ATTTTCTTGATGTCT[A/G]CAACATCGCTTTTTC	54778
rs749979833	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59017310	TCAGCATATGTGACA[A/G]TGCTTATTCATAAGA	54778
rs749985902	in-del	-/C			intron-variant	RNF111	GRCh38.p7	15:59040996	TTCATTTTTTTTCTT[-/C]AAAAATATACCCAAA	54778
rs749999952	in-del	-/TGTTCCC			utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096334	TGTATGTGGAGGACA[-/TGTTCCC]ATGGATCATATGTGA	54778
rs750001756	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59023878	ACTTTATAACTTTGA[A/G]CCTTGAGACCCTAAG	54778
rs750044191	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59059749	ATATCCTTTGTTTAA[C/T]TGAGCCTTAAACTAA	54778
rs750044825	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58991901	GAAATCTGAATATGG[A/G]TGGGTATTAGATGAT	54778
rs750073146	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59013548	TTTCTCATCACATTG[-/T]TATCAGGAGTACATG	54778
rs750091593	snp	A/T	1.64757e-05	0.00287012	missense	RNF111	GRCh38.p7	15:59081181	ACACACCAGCCAATT[A/T]CGCACCATATTCCAG	54778
rs750125193	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59087380	GTTACCACTTGAACA[A/G]TGCAGAGGTTAGGGG	54778
rs750125728	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59006887	CGCCTCCCGGGTTCA[A/G]GCAGTTCTCTGCCTC	54778
rs750166152	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58991143	CTAAAAAAAAAATAC[A/G]AAAATTAGCTGGGCA	54778
rs750215908	snp	C/G	1.65239e-05	0.00287431	missense	RNF111	GRCh38.p7	15:59067061	GAGCAAATAGTAGTT[C/G]TGGTACCAGCTATCA	54778
rs750220844	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59011394	TCATTCTTGTGTTTA[A/C]AATACTTGGGGCATT	54778
rs750229979	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59069881	GAGTGCCAGATTGTG[C/T]GTAGTCAAATAAAAA	54778
rs750233886	snp	A/G			utr-variant-3-prime	RNF111	GRCh38.p7	15:59095874	CACTGGCAGGTATCT[A/G]TGCATTCATAGAACT	54778
rs750245063	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59028321	AGTATGGTAGTCTGC[A/G]CCCCTGTCCAAGGGG	54778
rs750257798	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59037720	GCATGCCTGTAATCC[C/T]AGCTACTTGGGAGGC	54778
rs750303038	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59053084	TGTTACTCATTGATA[A/C]CAGTGAAACTTGTGC	54778
rs750310749	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59001465	CTATCAGTTTAGTGG[G/T]GATTGGAGGGAGATT	54778
rs750345539	snp	A/G	3.17808e-05	0.00398615	intron-variant	RNF111	GRCh38.p7	15:59055651	AAATTCTTTATTTAT[A/G]TTTACTAACTTAATA	54778
rs750349322	in-del	-/TCCTC			intron-variant	RNF111	GRCh38.p7	15:59061834	TCACACTAAACTCTT[-/TCCTC]TAATGGGCTTCTGAC	54778
rs750373558	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59011605	CTTCTTGGTTTATAA[A/G]TGATCGCTTGCTGTG	54778
rs750382347	in-del	-/TGGTATGTGGGAAAC			intron-variant	RNF111	GRCh38.p7	15:59035155	ACTACCATGAGAACA[-/TGGTATGTGGGAAAC]TGCCCCCATGAATTA	54778
rs750390002	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59002053	GGTTAATGACATGGG[C/T]ACTGTGTAGGCATTC	54778
rs750490560	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59073044	GGGTGCAGTGGCACG[C/T]GCCTGTGGTCCTAGC	54778
rs750543098	snp	A/C	3.70103e-05	0.0043016	intron-variant	RNF111	GRCh38.p7	15:59055879	AGTAGAAAATTATGA[A/C]AGGAGTTTGATAAAA	54778
rs750573150	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59090140	CCTTTGTAGCTAAAT[A/G]TCTTGTTTGAATTTT	54778
rs750603857	snp	A/C	1.64866e-05	0.00287106	synonymous-codon	RNF111	GRCh38.p7	15:59076172	GCCCCAGCCCCCTCC[A/C]CAGCCCTCTCTCTCA	54778
rs750613933	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59042583	TTTAACATTTAGAGC[A/T]TAGATCCATTTGGTG	54778
rs750627063	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59004412	ATTAGGATTAAGGTT[A/G]CTATTTTTATCTAGA	54778
rs750642123	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59031743	CATGGAACCTATTGC[A/G]TTGCATTTGTGCTTA	54778
rs750652441	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59084740	TGAAGCTTTGTACCC[A/G]TCGACCAGCATCTCC	54778
rs750682123	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59072149	CTTTTTGCTGATGGA[C/G]GGTCTTGCCTTAATG	54778
rs750706640	snp	C/T	1.64738e-05	0.00286995	utr-variant-3-prime	RNF111	GRCh38.p7	15:59094927	AGAACTCTTGCCCTC[C/T]CTCTCATTCCCATCC	54778
rs750739528	snp	C/G			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986499	TGGGATTACAGGCGT[C/G]AGCCACCGCGCCCAG	54778
rs750758396	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58989742	TGTTGTGATGTTTAA[A/G]AGAAAAGCACCTTGC	54778
rs750766889	in-del	-/TTTT			intron-variant	RNF111	GRCh38.p7	15:59000165	ATTTTTTTTTTCCCT[-/TTTT]TTTTTTTTTTTTTGA	54778
rs750781993	snp	C/G	1.64917e-05	0.00287151	synonymous-codon	RNF111	GRCh38.p7	15:59031566	TCGAAGAAAATATGC[C/G]TTGCTACCTAGTTCT	54778
rs750795200	snp	C/T			utr-variant-3-prime	RNF111	GRCh38.p7	15:59095213	TGCAGGCAAGGTTAG[C/T]TGCTTTAGTAAGTAG	54778
rs750797999	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59054663	ATTTTATTTTAGAAT[G/T]TGAACTTTTTAAACT	54778
rs750868157	snp	G/T	4.97657e-05	0.00498802	missense	RNF111	GRCh38.p7	15:59031650	TGAAGGAGAAGAAGA[G/T]TTGTTTGTTTCTGCC	54778
rs750883583	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59006118	GATTTTATTAGGGTG[A/G]TGGGATTGGGACTTA	54778
rs750909745	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59093763	TTATTGCCCTAATTT[A/G]TAAGGATAACTTTGT	54778
rs750912027	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59012935	GTTGAGACGGGGTTT[C/T]GCCATGTTGGCCAGG	54778
rs750916413	snp	A/G	4.95987e-05	0.00497965	synonymous-codon	RNF111	GRCh38.p7	15:59085764	ACTTCATCACTTACA[A/G]TTAGGAGCTCTTCCT	54778
rs751052927	snp	A/G	1.64751e-05	0.00287007	missense	RNF111	GRCh38.p7	15:59031228	GATTCCTCTTTTAGT[A/G]ATTGTCTTTCTTCTC	54778
rs751053318	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59087245	AGTGACAAGAGGGTG[A/G]AAAAACCTTAGAGAA	54778
rs751075031	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59089236	AAAATTAGAAAACAG[C/T]GTTAAAAGTTTCCCT	54778
rs751100878	snp	A/C	1.64762e-05	0.00287016	missense	RNF111	GRCh38.p7	15:59081185	ACCAGCCAATTTCGC[A/C]CCATATTCCAGCCAC	54778
rs751118380	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59005924	ATTAATAATTTGCTA[A/C]TGAGTCACAGCAGTG	54778
rs751135892	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59074484	CACTTTTATCTTATA[C/G]AGATAGCTTCTTTCC	54778
rs751143495	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:58990520	CCGAGCTTAGTGGTG[G/T]GCGCCTGTAGTCCCA	54778
rs751152027	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59017277	AGTTTGATTTTCCAG[A/G]GATCGTAAATGCGTC	54778
rs751155118	snp	C/T	1.64914e-05	0.00287149	missense	RNF111	GRCh38.p7	15:59066808	GTAACGGAAACTGGC[C/T]CTCCTGCAATGCCAA	54778
rs751185993	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59069819	GTAGAGGAGCAGAAG[A/C]AGCAAACAAAACCTG	54778
rs751186862	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59027521	AATAAAAGAAATTCT[A/G]TACCTTTTTTTCTTT	54778
rs751203892	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59001972	AATTGTGTGAATGTC[A/G]TCTCTCAAAATATTG	54778
rs751217679	snp	C/T	1.72829e-05	0.00293959	missense	RNF111	GRCh38.p7	15:59081284	TGATGCAGCATCCAA[C/T]GTATGTTTTACGTTT	54778
rs751230092	snp	A/G			downstream-variant-500B	RNF111	GRCh38.p7	15:59097641	TCCCAGCACTTTGGG[A/G]GGCTGAGGTGGGCAG	54778
rs751278924	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59016613	CCCACCATAATTTTG[G/T]TCTACCCTACCTATT	54778
rs751280749	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59053408	GAATCTTAATTTTTG[G/T]GTTGGAACGAATTTA	54778
rs751284427	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59051000	CAGGATTCTATTTAT[A/G]TAATCTTATCTAATG	54778
rs751344693	snp	C/G	1.64849e-05	0.00287092	missense	RNF111	GRCh38.p7	15:59075985	ACCTGAGCAACAGTG[C/G]TATCAGAAGTCATGG	54778
rs751344757	snp	A/G	2.67369e-05	0.00365619	intron-variant	RNF111	GRCh38.p7	15:59055663	TATATTTACTAACTT[A/G]ATATTGATGTCATTT	54778
rs751434896	snp	A/G	1.66671e-05	0.00288674	missense	RNF111	GRCh38.p7	15:59055747	GTTCTCATGCAAGTC[A/G]GCCACAGGAGCCACG	54778
rs751454541	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59026610	AATTTAGAATATTAT[C/T]TGTTATATTTGCTGC	54778
rs751495450	snp	C/T	0.206129	0.246121	intron-variant	RNF111	GRCh38.p7	15:59093363	TTTTTTTTTTTTTTC[C/T]TTTTCTGGGAGATGG	54778
rs751566517	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59041515	CCGAGATCTAGAGAT[C/T]GTGCCACTGCACTCC	54778
rs751583310	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59071020	TACGAAGAAGTGGCC[A/G]GGCGCGGTGGCTCAC	54778
rs751587923	snp	G/T	1.65247e-05	0.00287438	intron-variant	RNF111	GRCh38.p7	15:59094752	TTATCATAAAATTAA[G/T]TTTTGCTTTTTGTTT	54778
rs751642989	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58992296	GTGATTCGCCCGTCT[C/T]GGCCTCCCAAAGTGC	54778
rs751651059	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59029858	CTATAAACTTAGAAT[A/T]TGTGTGTATGCTATA	54778
rs751672919	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59071994	AAAAAATGTACATGC[C/T]TCAATTTAAAAATAC	54778
rs751686605	in-del	-/T	0.000460299	0.0151637	intron-variant	RNF111	GRCh38.p7	15:59067109	TTGAGTCAGTCTTTC[-/T]TTTCCTGCCCCTCTT	54778
rs751706955	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59035246	AGGTGAGATTTGGGT[A/C]GGGATACAGCCAGAC	54778
rs751735826	in-del	-/TTTTTTTTT			intron-variant	RNF111	GRCh38.p7	15:58996651	TCATCAGTACTTTCT[-/TTTTTTTTT]TTTTTTTTTTTTTTT	54778
rs751760597	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59040589	CTTACACTGAAAACT[C/T]TGATTCTTAACAATA	54778
rs751762200	snp	A/G			intron-variant, utr-variant-5-prime	RNF111	GRCh38.p7	15:58988185	GGAAGGCTGGGGTCG[A/G]TGACCGGCCGGTTAT	54778
rs751767716	snp	A/G	1.64738e-05	0.00286995	synonymous-codon	RNF111	GRCh38.p7	15:59058495	CCAACCTTCCACAGT[A/G]TCAGAGACTTCAGCT	54778
rs751779995	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59054376	TTGCAGTTGCTCCAT[C/G]TAGTACAATATGATG	54778
rs751817408	snp	C/T	1.65037e-05	0.00287256	synonymous-codon	RNF111	GRCh38.p7	15:59084186	CCCAAACTATGGTCA[C/T]GGGCATCATATTCAT	54778
rs751843366	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59003142	TTTTTTCGAGACAAG[G/T]TCTCACTCAGTTTCG	54778
rs751855551	snp	C/T	3.30289e-05	0.00406366	missense	RNF111	GRCh38.p7	15:59031439	GTTTACATGGCAGTT[C/T]GTTACGGAGACTTCC	54778
rs751868104	snp	A/G	1.72627e-05	0.00293786	intron-variant	RNF111	GRCh38.p7	15:59031738	TAAAACATGGAACCT[A/G]TTGCATTGCATTTGT	54778
rs751882215	snp	C/T	3.29576e-05	0.00405928	synonymous-codon	RNF111	GRCh38.p7	15:59089693	GGCAGGCTATCCTCA[C/T]ATCCGTTACATTTCA	54778
rs751885034	snp	A/G			upstream-variant-2KB	RNF111	GRCh38.p7	15:58987100	GAAGTCTGCCTGATG[A/G]ACTCTGAAGCTCATC	54778
rs751916273	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:58998635	ACTTGGATATTTGTA[C/G]ATATTTTCTCAAAAA	54778
rs751955530	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59065065	AGCTAGGTACTTTGA[G/T]CCCCATAGGAGCAGG	54778
rs751970190	snp	C/G	1.64741e-05	0.00286998	missense	RNF111	GRCh38.p7	15:59076092	CATCAGGCCGCTGCT[C/G]CTGCCCCAAGTCAAC	54778
rs751973622	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59053419	TTTGTGTTGGAACGA[A/G]TTTAGAAGTGCATTT	54778
rs751974009	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59066342	CAGCCGGGGTGTGGT[C/G]GCTCACGCCTGTAAT	54778
rs751999794	snp	G/T			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022155	ATGAGCCACCACGCC[G/T]GGCCAAGCTTCCTAT	54778
rs752000047	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59023757	GATTTTAATGAGAAT[A/G]CCTATAGTGTTTCAC	54778
rs752009430	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59046313	ATCCTCCCACGTCAG[C/T]CTCCTGGGTAGCTGG	54778
rs752023471	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:58997447	ACTAATGGCCCTGTA[G/T]CACAAATCAAGACAG	54778
rs752035556	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59023039	ATCACCTGAGGTCAG[C/G]AGTTCGAGACCAGCC	54778
rs752066882	snp	C/G	1.65844e-05	0.00287957	intron-variant	RNF111	GRCh38.p7	15:59091036	TCTTGGCTTTTACCA[C/G]TCATTATATTCTTCA	54778
rs752094006	snp	A/G	5.43966e-05	0.00521492	missense	RNF111	GRCh38.p7	15:59030823	TCCTTAAAGTTTCCC[A/G]TGTCTCAATGGACTC	54778
rs752099451	in-del	-/AAGA			intron-variant	RNF111	GRCh38.p7	15:59008239	TTTGTTTTTGGAGAC[-/AAGA]AAGAGTCTTTCTCTG	54778
rs752130154	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59045674	TCGTTGATACATAAT[A/G]CTTTTAGTTTTAAAT	54778
rs752185852	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59068536	ACTTTAACTTTAGAG[A/G]TGGAGGTTGTAGTGA	54778
rs752206489	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59057541	GGATTTATTCCTACC[A/G]TTCTCAATTTTAAGC	54778
rs752244521	snp	C/T			utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096797	GTAATGGATGTACTA[C/T]TTTGCCACTGGAATA	54778
rs752245735	snp	C/T	1.64727e-05	0.00286986	missense	RNF111	GRCh38.p7	15:59066940	CACCATTTTCAACAT[C/T]ATCACCACCACCACC	54778
rs752246028	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59060529	TAGTGCCAGCTACTC[A/G]GAGACTGAGTCAGGA	54778
rs752269694	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59094505	GGGCATTGGCAGCTC[C/T]TGTACCAAAACAAAA	54778
rs752301043	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59027301	CAGCTGTTTCCAACA[C/T]ACATCATGAGACTTC	54778
rs752301969	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59015127	TTTAGATCAGTACTT[A/C]CTAGGACCAAAGTCG	54778
rs752305661	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58990135	CTTTGCTTGCTATAC[A/G]TTAGATCTCCGAGTT	54778
rs752328473	snp	C/T	3.3534e-05	0.00409461	intron-variant	RNF111	GRCh38.p7	15:59052254	AAAATTTCTGCCTAA[C/T]GATTAGCTGACAGGA	54778
rs752409820	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59061947	TGTGTTCTCATCCCC[C/G]CTTTCACTAGCCCAT	54778
rs752410079	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59001017	TTTTGCCTTTCCACA[A/G]AAATTTTAATGTTGG	54778
rs752418479	snp	A/T	5.01819e-05	0.00500884	intron-variant	RNF111	GRCh38.p7	15:59030773	ATAAAACACATTAAA[A/T]ATCTTTTAAATATCT	54778
rs752430861	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59080177	CCAGGCTGGGGTGCA[C/G]TGGCATGATCTCAGC	54778
rs752431930	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59032286	ATTTTATGTATGTTC[C/T]TCATTTATGGTACAC	54778
rs752515431	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59047864	ATAGGCGTGAGCCAC[A/T]GTATCCAGCCTACTT	54778
rs752526355	snp	C/T	1.64735e-05	0.00286993	utr-variant-3-prime	RNF111	GRCh38.p7	15:59094918	CCATGTTTCAGAACT[C/T]TTGCCCTCCCTCTCA	54778
rs752529147	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59009055	ACCTCCACCTCCTGG[A/G]TTCAAGCGATTCTCT	54778
rs752534750	snp	A/C	1.7969e-05	0.00299736	intron-variant	RNF111	GRCh38.p7	15:59055867	TGAAGTAGTAACAGT[A/C]GAAAATTATGAAAGG	54778
rs752539190	snp	G/T	1.64925e-05	0.00287158	intron-variant	RNF111	GRCh38.p7	15:59094764	TAATTTTTGCTTTTT[G/T]TTTTCTTGCCAATAA	54778
rs752562006	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59019220	CTGGGATTACAGGTG[A/T]GATCCATTTATTTAT	54778
rs752609282	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59036312	ATCCGCTGCCCACCT[C/G]AGCCTCCCAAAGTGC	54778
rs752610664	snp	A/G			missense	RNF111	GRCh38.p7	15:59031417	GGATTGTTAATGAAA[A/G]GACCCTGTTTACATG	54778
rs752634289	snp	A/C	1.64738e-05	0.00286995	missense	RNF111	GRCh38.p7	15:59081197	CGCACCATATTCCAG[A/C]CACAGCACCTCCAGC	54778
rs752637066	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59061177	CAAAAACTTTTATAT[A/G]TAAATCTTTGTTCAT	54778
rs752637436	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58992526	TTCATATTTTAAAAT[A/G]TATTTTTTTGGCTGG	54778
rs752654280	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58993146	CTGCCCTTCAGTCTG[A/G]GTGACAGAGCAAGAT	54778
rs752695764	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59053313	CATCTTATACTTTAG[A/G]TGATTATAAGTATTG	54778
rs752703105	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59093187	GCCACACAAGGTTTG[G/T]CCAGGGAAATTTCGT	54778
rs752718565	snp	C/T	1.66139e-05	0.00288213	intron-variant	RNF111	GRCh38.p7	15:59058585	AGGGGAGACTTTTTG[C/T]CATTACTTTCGTTAG	54778
rs752720216	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59081599	GTGAGGCTCATTCCC[A/G]TAATCCCCAGTTGCT	54778
rs752723912	snp	A/T	1.99416e-05	0.00315759	intron-variant	RNF111	GRCh38.p7	15:59081301	TATGTTTTACGTTTT[A/T]AAAAAGAAAGTCAAG	54778
rs752733371	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59089180	GGGTCAGTTCACACA[C/T]ATGTAATCCATAAAT	54778
rs752814276	snp	C/G	1.64996e-05	0.0028722	missense	RNF111	GRCh38.p7	15:59085663	CCTTTCGTTAGGGAA[C/G]TGGGAATTGAAGCTG	54778
rs752822374	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59064839	GAGAATCCGGAAAGG[A/C]AGGATAAGACATGTA	54778
rs752824052	snp	A/T	1.65184e-05	0.00287384	synonymous-codon	RNF111	GRCh38.p7	15:59031455	GTTACGGAGACTTCC[A/T]TGCAGAAAGAGATTT	54778
rs752865837	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59039770	TTGCCAGGCTGGAGT[A/G]CAGTGGTGCGATATT	54778
rs752903853	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59022975	AAATTGGCTGGGCGC[G/T]GTGGCTTACGCCTGT	54778
rs752919626	in-del	-/AAAC			intron-variant	RNF111	GRCh38.p7	15:59009956	AAGACCTTATCTCAA[-/AAAC]AAACAAACAAAAATT	54778
rs752935923	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59092118	AGTATTGAGGTATTA[C/T]CAGTACATTCAAGTT	54778
rs752974127	snp	A/G	1.77584e-05	0.00297974	missense	RNF111	GRCh38.p7	15:59030835	CCCATGTCTCAATGG[A/G]CTCCTGAATATAACG	54778
rs752991991	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59011658	GTGTGTTTGCATCCT[C/G]ATGTTGCTTTGTGTG	54778
rs753011514	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58995397	TATTTTGATGTTCAA[A/G]TTGTCCCAGATTTGT	54778
rs753065448	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59071298	GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA	54778
rs753087758	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59082438	GGAAAGTATTAATAG[A/G]ATTTTCAGTGAATGA	54778
rs753117492	snp	A/C/T			intron-variant	RNF111	GRCh38.p7	15:59063622	TTGGGTAGTAACTCT[A/C/T]GAATGAGAGGCTAAT	54778
rs753120680	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59075794	CAAGATAACCAAGTA[G/T]TTTGTTGGTGCTCAC	54778
rs753156115	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59001552	TTGATAATCATGACA[A/G]TTTTACCAGGAAAAA	54778
rs753197827	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59004893	AGAATCTGACAGCAT[A/G]GTAAGATGCTCACAT	54778
rs753209578	snp	A/G	3.34801e-05	0.00409132	intron-variant	RNF111	GRCh38.p7	15:59076262	GAGTCATGTCAATGA[A/G]GCATTTTGTACTTCC	54778
rs753216168	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59005778	GATTTCTAAAAACTA[G/T]CTGACTCGTCATCTT	54778
rs753297229	snp	A/G	1.64855e-05	0.00287097	missense	RNF111	GRCh38.p7	15:59058532	ACAAGCAATAGTACC[A/G]CTGGCACTTCTATAG	54778
rs753302267	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59086086	TTTTGCCGTAAGTGG[C/T]AATAGATCCGTTCTG	54778
rs753348986	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:58999928	CACAATTTTAAAAAA[A/C]CACATCTCATGAGAA	54778
rs753349082	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:58988600	CCTTCGATAATTTAT[C/G]AGAGTCAGTGTCAGT	54778
rs753351737	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59067204	CCTCCCTCCATTTCT[C/G]TCCCTGCTTTCTTCC	54778
rs753358872	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59036162	CTCACTGCAACCTCT[A/G]CCTCCTGGGTTAAAG	54778
rs753369131	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59070200	TGTGATGCATCATTT[A/G]TAATCTGTGTAAGCC	54778
rs753429905	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59007973	CTTTTGTTTTCTTAA[C/T]GCTGTCTCTGAAGAG	54778
rs753437068	snp	C/T			utr-variant-3-prime	RNF111	GRCh38.p7	15:59095326	ATCAATCATGTACTT[C/T]AGTTTAATGTATAAA	54778
rs753479026	snp	C/G/T	0.000153988	0.00877328	intron-variant	RNF111	GRCh38.p7	15:59092469	TTTTTCAAATAAACA[C/G/T]AGACTTTACTCAGTT	54778
rs753482058	snp	A/T	2.87162e-05	0.0037891	intron-variant	RNF111	GRCh38.p7	15:59052473	TTTGAAATATTAAAT[A/T]TAAATATTAAACATA	54778
rs753533371	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59077250	TTCAATATGCTTAAT[A/T]TTCTGCCCCTCCCCT	54778
rs753544946	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:58998971	CGAGCAGTTGTTTTT[G/T]CACTGATAGTATGAG	54778
rs753558922	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59071822	TAATACAAGCATACC[G/T]TGGAGATACTGCAGG	54778
rs753560165	in-del	-/TAA			utr-variant-3-prime	RNF111	GRCh38.p7	15:59095207	AAACTTGCAGGCAAG[-/TAA]GTTAGCTGCTTTAGT	54778
rs753573920	snp	A/G	3.29707e-05	0.00406008	missense	RNF111	GRCh38.p7	15:59030988	GCAGGAGTTGAGATG[A/G]TTAATAGTAAAGTGG	54778
rs753600024	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59089045	CAGAGCCCTGTTCTA[C/T]CTCAGCTGGGAACAG	54778
rs753635801	snp	A/G	9.89169e-05	0.00703197	synonymous-codon	RNF111	GRCh38.p7	15:59031359	TAGAAGCCATAGTGC[A/G]CGGTCTCATAAGTGG	54778
rs753660383	in-del	-/AG	1.64735e-05	0.00286993	frameshift-variant	RNF111	GRCh38.p7	15:59058498	ACCTTCCACAGTGTC[-/AG]AGACTTCAGCTACTC	54778
rs753683742	snp	A/G	1.65116e-05	0.00287324	intron-variant	RNF111	GRCh38.p7	15:59081316	TAAAAAGAAAGTCAA[A/G]TTTGCTTTTTCTTCT	54778
rs753721452	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58997612	TCACGAGGTCAAGAG[A/G]TCGAGACCATCCTGG	54778
rs753779520	in-del	-/A/AA			intron-variant	RNF111	GRCh38.p7	15:59073481	TGAGACACCATCTCC[-/A/AA]AAAAAAAAAAAAAAT	54778
rs753801145	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59003057	CTATTCACAGGTGCT[A/G]TTAAAGCTTACTGCA	54778
rs753828299	snp	A/T	1.65787e-05	0.00287907	missense	RNF111	GRCh38.p7	15:59031646	CAACTGAAGGAGAAG[A/T]AGATTTGTTTGTTTC	54778
rs753848401	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59017510	TATTTATAAAAACAT[A/C]AATTGTCTTTAGGTT	54778
rs753850492	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59070947	TCTTTATGATCTTTC[A/G]TCACATTTTGAAAAG	54778
rs753857039	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59091602	GCAATTTATTTTGAC[C/G]GACATTTTATTGATG	54778
rs753961250	in-del	-/AA			intron-variant	RNF111	GRCh38.p7	15:59064535	GCAAGACTTTGTCGC[-/AA]AAAAAAAAAAAAAAA	54778
rs753971706	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59074107	TTCTTAAAATATTCA[G/T]TAAACCACGTAAATA	54778
rs753982642	snp	C/T	1.65141e-05	0.00287346	synonymous-codon	RNF111	GRCh38.p7	15:59085755	ACCTCCTCGACTTCA[C/T]CACTTACAATTAGGA	54778
rs753985306	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59051389	TGTGAACCCAGGAGG[C/T]GGAGCTTGCAGTGAG	54778
rs753996618	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59091988	CACTCACCTCCTGCT[C/G]TGCAGCCAGGTACTG	54778
rs754019481	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58995316	AGAGACATTCTTTTA[C/T]CTGATTAATACAGAA	54778
rs754021714	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59022848	TGTCTAGGTTTTACT[C/T]TGGATCTGAGAAAAG	54778
rs754044424	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59039905	GTGTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT	54778
rs754047214	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59005400	TAGAGTAAAAACAAA[C/T]TTTATCTAAATAAAC	54778
rs754084447	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58994607	CTCAGCCTCCTGAGT[A/G]GCTGAGATTATAGGT	54778
rs754108552	snp	A/G	1.66427e-05	0.00288462	synonymous-codon	RNF111	GRCh38.p7	15:59055760	TCGGCCACAGGAGCC[A/G]CGGAACCGCAGTAGG	54778
rs754141488	snp	C/T	1.64741e-05	0.00286998	missense	RNF111	GRCh38.p7	15:59076084	TCTTTGGCCATCAGG[C/T]CGCTGCTGCTGCCCC	54778
rs754192204	snp	C/T	1.6476e-05	0.00287014	missense	RNF111	GRCh38.p7	15:59081022	CAGACTCAGCCTCCG[C/T]CTCAAGTGGATTATG	54778
rs754206926	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59057464	GTCAACCCTCTCATT[C/T]CATAGCACATTAAGA	54778
rs754212952	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59088674	GATCTATACAGTTGC[C/T]GCAAACACTGAATTA	54778
rs754229173	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59085060	AGGTGGAAGCAGATT[C/T]TCATTAGATTAATTT	54778
rs754243202	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59004582	TTTCCCCAAACCAGT[A/G]TTCTAGAGTTGTTTA	54778
rs754246288	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59086078	TTCAGTTATTTTGCC[A/G]TAAGTGGTAATAGAT	54778
rs754250521	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59056181	CAGTACTTTTTAAAT[A/G]TAAACACAAAAGCAG	54778
rs754271291	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59085949	TAGATGTATTAAAAT[A/C]TGCACGTATAATTTG	54778
rs754280706	in-del	-/ATC	3.3094e-05	0.00406766	intron-variant	RNF111	GRCh38.p7	15:59094739	TAACTACGTACAATT[-/ATC]ATAAAATTAATTTTT	54778
rs754294892	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59044092	CTGGAGTGCAGTGGC[A/G]CAATCTCGGCTCACT	54778
rs754310381	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59032049	GTTCAAGCAATTCTC[C/T]TGCGTCAGCCTCCCA	54778
rs754357012	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59053881	CTCTTATTGTTATTA[-/A]GAGATATTAATTTTG	54778
rs754392944	snp	C/G	1.64917e-05	0.00287151	missense	RNF111	GRCh38.p7	15:59031552	CGAGAAGTGTTAGCT[C/G]GAAGAAAATATGCCT	54778
rs754429185	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59089290	TAGGGTACTTTGGCT[G/T]TTAGGAAGCTTAACA	54778
rs754446370	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59003992	TTTCTTGGTTTTGTT[C/G]TCATTCCAGATGCTT	54778
rs754452046	snp	C/T	1.78653e-05	0.0029887	intron-variant	RNF111	GRCh38.p7	15:59066714	ACCTATTTTTTTACA[C/T]AGTGATATTTCATGA	54778
rs754471748	snp	C/T	0.00694604	0.0585215	synonymous-codon	RNF111	GRCh38.p7	15:59081192	AATTTCGCACCATAT[C/T]CCAGCCACAGCACCT	54778
rs754507452	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59028926	CTGGGATTACAGTCA[G/T]TGCGCCACTATCCTG	54778
rs754513283	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58988709	TCTTTACAGATGGGT[A/G]TTTCTCAACCTAAGT	54778
rs754522881	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:58995765	TGCCGTGCCCCGGCC[-/T]TTTTTTTTTTTTTTT	54778
rs754559032	snp	C/T	1.66369e-05	0.00288412	synonymous-codon	RNF111	GRCh38.p7	15:59031674	TTCTGCCAGTGAAAA[C/T]CACCAAAACAATCCA	54778
rs754695517	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59078751	GTAATCGCAGCTACT[C/T]GGGAGGCTGAGGCAG	54778
rs754713651	snp	C/T	2.41619e-05	0.00347568	intron-variant	RNF111	GRCh38.p7	15:59055668	TTACTAACTTAATAT[C/T]GATGTCATTTAAGGT	54778
rs754721530	snp	C/T	3.46741e-05	0.00416363	intron-variant	RNF111	GRCh38.p7	15:59031744	ATGGAACCTATTGCA[C/T]TGCATTTGTGCTTAA	54778
rs754759983	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59048565	TTACTAAAATTAGCA[A/C]AATGTACACTTAAAA	54778
rs754765349	snp	C/G	1.64893e-05	0.0028713	missense	RNF111	GRCh38.p7	15:59031018	GGGAATGAATTCTCT[C/G]ACCTGTGTGATGATT	54778
rs754803528	snp	C/G	1.66665e-05	0.00288669	missense	RNF111	GRCh38.p7	15:59055749	TCTCATGCAAGTCGG[C/G]CACAGGAGCCACGGA	54778
rs754806190	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58992230	TTGTATTTTTAGTAG[A/G]AACGGTTTTTCACCA	54778
rs754807351	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59007990	CTGTCTCTGAAGAGC[A/G]GAGGTTTTGATTTTG	54778
rs754823110	in-del	-/ATC			intron-variant	RNF111	GRCh38.p7	15:59074702	GTGTTTCAGTTTCTT[-/ATC]ATTTGTGTGTTCACT	54778
rs754833764	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59035051	GGTGAATGAAGAGCA[A/G]AGTCACGTCTTACAT	54778
rs754845349	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59070952	ATGATCTTTCATCAC[A/G]TTTTGAAAAGTATGG	54778
rs754849606	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59047848	CCAAAGTGCTGGGAT[A/T]ATAGGCGTGAGCCAC	54778
rs754853595	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59050822	AAGTTTTAAACATAC[A/G]ATACGTTATTGCTAA	54778
rs754864971	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59013996	AGGTTTCACTATATT[G/T]CCCAGGCTGGTCTTG	54778
rs754870272	snp	C/T	0.000188377	0.00970325	intron-variant	RNF111	GRCh38.p7	15:59093419	GCAGCAGTCTCAGCT[C/T]ACTGCAACCTCCACC	54778
rs754887959	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59087605	AATGTTAAGAAAATT[A/G]TAAGGAAGGGAAAAT	54778
rs754923078	snp	A/C	1.64806e-05	0.00287054	missense	RNF111	GRCh38.p7	15:59031104	CGTTGTGAGGAAAAA[A/C]CGCAAAAGCCAGCAG	54778
rs754952852	snp	G/T	1.65217e-05	0.00287412	intron-variant	RNF111	GRCh38.p7	15:59094753	TATCATAAAATTAAT[G/T]TTTGCTTTTTGTTTT	54778
rs754961280	snp	A/G	1.64741e-05	0.00286998	missense	RNF111	GRCh38.p7	15:59081095	CTCATGCAACATCTC[A/G]TCCTGTGGCACCCCC	54778
rs754982869	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59037875	ATTATATCTCCTTCA[A/G]TCTTCAAGGAAACGT	54778
rs755001570	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59062376	CAATTGCTTCTTGGA[C/T]ATCTCTCCTGGACCG	54778
rs755018043	snp	C/G/T			intron-variant	RNF111	GRCh38.p7	15:59011610	TGGTTTATAAATGAT[C/G/T]GCTTGCTGTGTTCTC	54778
rs755021808	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59046556	TAGACCTTTTACCTG[-/T]TTGTCTGACACAGAA	54778
rs755032597	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59072218	ATTGGGGTGGCTGTG[A/G]CAATTTCTTGAAGTA	54778
rs755056006	in-del	-/T/TT			intron-variant	RNF111	GRCh38.p7	15:58994033	TTGTTGTTACTTAAA[-/T/TT]TTTTTTTTTTTTTTT	54778
rs755058114	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59012045	TTTGAGATGGAGTCT[C/G]GCTCTGTCACCCAGG	54778
rs755061798	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59065919	AGGAGGCTGAGGCAG[A/G]AGAATCTGTTGAGCA	54778
rs755097097	snp	A/G	2.93242e-05	0.003829	intron-variant	RNF111	GRCh38.p7	15:59084063	GGGATTTTTTTCTAC[A/G]TTAAGAAAAGAAATA	54778
rs755103520	in-del	-/TATTT			intron-variant	RNF111	GRCh38.p7	15:58992038	CTTGCAAATGTCTGG[-/TATTT]TATTTTATTTTATTT	54778
rs755182498	in-del	-/TTTA			intron-variant	RNF111	GRCh38.p7	15:59052515	GATATTTGCATTCTT[-/TTTA]TTTATTTATTTTTGA	54778
rs755199009	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59074112	AAAATATTCAGTAAA[A/C]CACGTAAATAGCTGT	54778
rs755252545	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59049629	TTTTGGCAAGAATTT[C/T]GTTTGTTACAGCATT	54778
rs755260805	in-del	-/GTT	1.64827e-05	0.00287073	cds-indel	RNF111	GRCh38.p7	15:59031090	CAAGAAAAAAGTCTC[-/GTT]GTGAGGAAAAAACGC	54778
rs755288571	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59063434	AGGCACTCCTAGGAG[A/G]CACTTTAACCAAATT	54778
rs755294465	snp	C/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022233	CCTCTTAGTGGTTTT[C/G]TCTGTTAGCTAGTTC	54778
rs755302766	snp	C/G	1.64784e-05	0.00287035	missense	RNF111	GRCh38.p7	15:59089732	GGATGGAACATCATT[C/G]AGAGGTCCTTTCAGG	54778
rs755320595	snp	A/T	1.65707e-05	0.00287838	intron-variant	RNF111	GRCh38.p7	15:59091040	GGCTTTTACCAGTCA[A/T]TATATTCTTCACTTT	54778
rs755335566	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59000574	AACAGCCAGGTATGG[-/T]TGGCGGGCGCCTATA	54778
rs755344204	snp	A/G	0.000259235	0.011382	intron-variant, missense	RNF111	GRCh38.p7	15:59004174	GATTAGCAGTTTTAA[A/G]GTCTCAACTTTGTTT	54778
rs755354938	snp	C/G/T			intron-variant	RNF111	GRCh38.p7	15:58994727	AAGTGATCAGCCTAC[C/G/T]TCAGCCTCCCAAAGT	54778
rs755392760	snp	C/T	3.29473e-05	0.00405864	synonymous-codon	RNF111	GRCh38.p7	15:59076097	GGCCGCTGCTGCTGC[C/T]CCAAGTCAACCTTTA	54778
rs755408241	snp	C/T	1.64944e-05	0.00287175	missense	RNF111	GRCh38.p7	15:59076189	AGCCCTCTCTCTCAT[C/T]ATGTCGACATTACAT	54778
rs755415396	snp	A/G			synonymous-codon	RNF111	GRCh38.p7	15:59076022	CAGTTTTCATGGAGC[A/G]TCTGCATTTGACCCC	54778
rs755419018	snp	G/T			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021169	TTTTTTTGTTTGTTT[G/T]AGATGAAGTCTTGCT	54778
rs755440517	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59003963	TAAAATTAATTTCTC[A/T]TTCCTGATTGACTTT	54778
rs755482466	snp	A/G			utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096791	TAGCCTGTAATGGAT[A/G]TACTACTTTGCCACT	54778
rs755514439	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59072292	TGAAAGATTTCTCTG[C/T]AGCACATGATGCTGT	54778
rs755530333	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59084047	TATAGTATTAATACT[A/G]GGGATTTTTTTCTAC	54778
rs755550606	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59085090	TTCTGAATCCATTGT[A/G]TGTGGGCATTCATTG	54778
rs755567587	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59042875	TCCTCCAAGTGAACT[C/T]TATAATCAGTTTGTT	54778
rs755598397	snp	A/C	1.64765e-05	0.00287019	missense	RNF111	GRCh38.p7	15:59058413	AAGCTACTAGCGCTT[A/C]CATTAACAATTCAAA	54778
rs755631504	snp	A/C	1.64735e-05	0.00286993	missense	RNF111	GRCh38.p7	15:59066946	TTTCAACATCATCAC[A/C]ACCACCACCATACTC	54778
rs755633906	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59024001	AGTTTACCAATAATA[C/T]ATAGGAAAAAATCTT	54778
rs755650163	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58997940	AGCTGAGTCTCACTC[C/T]GTTGCCCAGGCTGGA	54778
rs755662516	snp	A/C/G	3.29991e-05	0.00406185	intron-variant	RNF111	GRCh38.p7	15:59089762	GGGCAATTTTGAGGT[A/C/G]TGTAATAAAATAAAT	54778
rs755666384	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59007559	ATTCACGTTTTCCAA[C/T]TTAGGCATGGAATTA	54778
rs755708282	snp	C/T			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986951	GTTCAGAGCATTATA[C/T]AAATTGTCTCATTTA	54778
rs755717270	snp	A/G	1.67385e-05	0.00289292	intron-variant	RNF111	GRCh38.p7	15:59052256	AATTTCTGCCTAACG[A/G]TTAGCTGACAGGAAG	54778
rs755729003	snp	A/C/T	3.29489e-05	0.00405874	missense	RNF111	GRCh38.p7	15:59076078	CTGCAATCTTTGGCC[A/C/T]TCAGGCCGCTGCTGC	54778
rs755748814	snp	A/T	1.65471e-05	0.00287633	intron-variant	RNF111	GRCh38.p7	15:59091046	TACCAGTCATTATAT[A/T]CTTCACTTTCAGGAA	54778
rs755759486	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59089540	TTGGAGTTATGTATT[C/G]TTATTGAAGTCAAAT	54778
rs755778922	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59006716	AAATAAAGTTACAGA[C/T]GCCAGTGCATTTTAC	54778
rs755807411	snp	A/G	3.29609e-05	0.00405948	missense	RNF111	GRCh38.p7	15:59052373	ACTGCCAATGAAGAA[A/G]TTAATGTTACCTCAA	54778
rs755823235	snp	C/T	8.24328e-05	0.00641947	intron-variant	RNF111	GRCh38.p7	15:59094769	TTTGCTTTTTGTTTT[C/T]TTGCCAATAATAGAC	54778
rs755848375	in-del	-/C			intron-variant	RNF111	GRCh38.p7	15:59074970	CCAAAGAGAGGAGAG[-/C]CAGGGTAATGGGGAA	54778
rs755861871	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59082084	CCCTGTCTCTCCCCC[-/T]CTCCCCAAAAAAGTA	54778
rs755864371	snp	C/G	1.76864e-05	0.0029737	missense	RNF111	GRCh38.p7	15:59030838	ATGTCTCAATGGACT[C/G]CTGAATATAACGAGC	54778
rs755879926	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:58991175	GGTGGTGGCATGCGC[C/G]TGTAATCCTGGCTGC	54778
rs755908608	snp	A/C	1.64757e-05	0.00287012	missense	RNF111	GRCh38.p7	15:59031252	TCTTCTCCTTCATCT[A/C]GTCTGCATTTTGGAG	54778
rs755913484	snp	A/C	1.64746e-05	0.00287002	synonymous-codon	RNF111	GRCh38.p7	15:59081198	GCACCATATTCCAGC[A/C]ACAGCACCTCCAGCA	54778
rs755916110	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59058612	TTAGGAAAAGTATTA[C/T]TGTTTTTAAGTCTAA	54778
rs755943393	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59086401	TGGGATTACAGGCTT[A/G]AGCCAGGGCACCCAG	54778
rs755981584	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59029154	ATTTCCATCAGCAAT[A/G]TATGAGGGTTCCAAT	54778
rs755982775	snp	G/T	1.64735e-05	0.00286993	utr-variant-3-prime	RNF111	GRCh38.p7	15:59094920	ATGTTTCAGAACTCT[G/T]GCCCTCCCTCTCATT	54778
rs755986990	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59081573	TAATGTAACTTGTAA[C/G]TATAAGCTGGGTGAG	54778
rs756006496	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58992527	TCATATTTTAAAATA[C/T]ATTTTTTTGGCTGGG	54778
rs756009553	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59051457	GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAGGAA	54778
rs756044475	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59027741	TTTCACCATGTTGGT[C/T]AGGCTGGTCTCAAAC	54778
rs756046644	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59051514	GGTGCAGTGGCTCAC[A/G]CCTATAATCCCAGCA	54778
rs756077953	snp	A/G	4.02164e-05	0.00448403	intron-variant	RNF111	GRCh38.p7	15:59081302	ATGTTTTACGTTTTT[A/G]AAAAGAAAGTCAAGT	54778
rs756080307	snp	A/T	3.30726e-05	0.00406635	missense	RNF111	GRCh38.p7	15:59084224	AGACTATGTCCTCAC[A/T]TCCTCGACAGGCTCC	54778
rs756099196	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59068865	GTGGATCACGAGATC[A/G]GGAGTTCGAGACCAG	54778
rs756117381	snp	C/T	0.000148267	0.00860879	missense	RNF111	GRCh38.p7	15:59066841	TTACCTTCCTGCTGT[C/T]CCCAGCACTCACCAT	54778
rs756133435	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59062327	GGATTACAAGTGTGA[A/G]CCACCATGCCCGGCC	54778
rs756146989	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59039795	GATATTGGCTCAGTA[C/T]AACCTCTGCCTCCCA	54778
rs756149469	snp	C/T			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022004	AGCTGGAACTACAGG[C/T]GCGTGCCACCATGCC	54778
rs756182104	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59049192	ACTCCTCTTTCTCCT[C/T]GCTCTGACCCTGGTT	54778
rs756191253	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59069898	TAGTCAAATAAAAAT[C/T]AGACTGGCATACCGA	54778
rs756198549	in-del	-/TTC			intron-variant	RNF111	GRCh38.p7	15:59002111	TATTTCTAGAGTTTT[-/TTC]TTTAATATTTTTGGA	54778
rs756201945	snp	A/C			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021058	GTGTAGTCTTTTATC[A/C]CTGACCTCACTTTCC	54778
rs756247246	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58993382	AATATAACTGTAAAT[A/G]CAAAAATTAGCTGGG	54778
rs756267376	snp	C/T	1.64974e-05	0.00287201	synonymous-codon	RNF111	GRCh38.p7	15:59085671	TAGGGAACTGGGAAT[C/T]GAAGCTGGAGTGACT	54778
rs756327399	snp	C/T	5.16596e-05	0.00508204	intron-variant	RNF111	GRCh38.p7	15:59075914	CATGAAATATTTGAC[C/T]AAACTTTAGAAAGAT	54778
rs756372080	in-del	-/TCTC	4.03319e-05	0.00449047	intron-variant	RNF111	GRCh38.p7	15:59067126	TTCCTGCCCCTCTTG[-/TCTC]TCTCTCTCTCTCCTT	54778
rs756394620	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59083571	ATCAAGCTAAATACA[C/T]GTTTCCTAGGTGTGT	54778
rs756397210	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59061283	AGGACCCTATGGAAC[A/G]TTAGTTCAACTATGT	54778
rs756410778	in-del	-/AATA			intron-variant	RNF111	GRCh38.p7	15:59051784	CTCAATAAATAAATA[-/AATA]AATAAATAAATAAAT	54778
rs756460511	snp	C/G/T			intron-variant	RNF111	GRCh38.p7	15:59013937	GGGGTTACAGGCACA[C/G/T]GCCACCACGCCTGGC	54778
rs756477437	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59041769	GGTGCCTGTTTTCTC[A/G]AAATCCTTCCAACAG	54778
rs756494985	snp	C/T	3.59745e-05	0.00424098	intron-variant	RNF111	GRCh38.p7	15:59080887	TAATAGCAATATATG[C/T]TCAACTGCATGGTGC	54778
rs756524774	snp	A/G	3.29473e-05	0.00405864	synonymous-codon	RNF111	GRCh38.p7	15:59058432	TAACAATTCAAATCC[A/G]TCTACCTCTGAGCAG	54778
rs756551922	snp	C/G	1.64912e-05	0.00287147	missense	RNF111	GRCh38.p7	15:59058536	GCAATAGTACCACTG[C/G]CACTTCTATAGGAGG	54778
rs756573864	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58988458	GCCCTGACGGCTAGG[A/G]AGTCGCCTGCTGCTG	54778
rs756637954	snp	G/T	3.30393e-05	0.0040643	missense	RNF111	GRCh38.p7	15:59031460	GGAGACTTCCATGCA[G/T]AAAGAGATTTGTAAA	54778
rs756661486	snp	C/T	9.89479e-05	0.00703307	missense	RNF111	GRCh38.p7	15:59031378	TCTCATAAGTGGCCT[C/T]GGACTGAGACAGAAT	54778
rs756705278	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59054807	CCTTTTATATTACAG[A/G]TATTTTCTGTAAATG	54778
rs756740823	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59082695	GTTACAACAGAGAAC[A/G]TACGGCCTGTAGAGC	54778
rs756750650	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59087271	GAGAATGACAATACT[A/G]TATTTAAATGATAAT	54778
rs756762707	in-del	-/TG			intron-variant	RNF111	GRCh38.p7	15:58990184	GGCTTCAGGTCTCTC[-/TG]TTTAAATGAGAATTG	54778
rs756766462	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59068298	ATATACTATTCCAGA[A/C]AAAAAGTGCTGCAAA	54778
rs756778600	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59033971	TAATAACATTCACAC[A/G]ATATGGAATTTTAAA	54778
rs756788937	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59047985	TGAGGATGTGGAGAA[C/T]CTGAAACCTTCATTT	54778
rs756794225	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:58989047	CCATTTCCTTTCCCA[-/T]TTTTTGTTGTGTGTG	54778
rs756795801	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59083291	TTGGCTCATGTCTGT[-/A]AATCCCAGCACTTTG	54778
rs756810860	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59011279	ATTAAGTTTCAGTGC[A/C]TACCTCTATCATAAC	54778
rs756811597	snp	C/T	1.6528e-05	0.00287467	missense	RNF111	GRCh38.p7	15:59076212	CATTACATGCCACCC[C/T]CTTGTAAGTATATAC	54778
rs756829611	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59069838	AAACAAAACCTGAGA[A/T]TTGTGATTTTGTAGA	54778
rs756831994	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58991066	TTTGGGAAGCCGAGG[C/T]GGGTAGATCATGAGG	54778
rs756838051	snp	G/T			downstream-variant-500B	RNF111	GRCh38.p7	15:59097645	AGCACTTTGGGAGGC[G/T]GAGGTGGGCAGATCA	54778
rs756872319	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59086182	TGGAGTGCAGTAGTA[C/T]GATCTCAGCTCACTG	54778
rs756903224	snp	C/T	7.16499e-05	0.00598497	intron-variant	RNF111	GRCh38.p7	15:59080906	ACTGCATGGTGCCTA[C/T]GTAACATACTCAAAA	54778
rs756906079	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59057723	TAAAAAGGCATGGAA[A/G]GGAGATTAAAACAGT	54778
rs756919052	snp	C/T			upstream-variant-2KB	RNF111	GRCh38.p7	15:58987180	CTTTTATAAAATAAA[C/T]AAGGAGGCTTATGCG	54778
rs756921097	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59058586	GGGGAGACTTTTTGT[C/T]ATTACTTTCGTTAGG	54778
rs756972220	in-del	-/TTTAA			intron-variant	RNF111	GRCh38.p7	15:59040494	AGAAAAAAATAAATC[-/TTTAA]TTTAAGTGAATATTT	54778
rs757021745	snp	C/T	1.64743e-05	0.00287	missense	RNF111	GRCh38.p7	15:59066964	CACCACCATACTCCC[C/T]ACCCAGCTGTCCCAG	54778
rs757026474	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59068681	TTAAGCCACCGTGCC[C/T]GGCCAAGCTACCACT	54778
rs757068158	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59038882	TGATCCTTCCATTAT[A/G]AAGTTCCCCTTCACT	54778
rs757069129	snp	C/T			utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096921	CACAGGTGGATTTCT[C/T]TATTTTTGAATACTA	54778
rs757090806	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59010268	ATAAACCCATGACAT[A/G]TAAATATAAATAGTA	54778
rs757094417	snp	C/T	3.30104e-05	0.00406252	synonymous-codon	RNF111	GRCh38.p7	15:59084171	TCCACATAGGATGCA[C/T]CCAAACTATGGTCAT	54778
rs757100859	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59068310	AGAAAAAAAGTGCTG[C/T]AAAAAAAGTCAAAGA	54778
rs757110186	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59026649	TTAAATGCAATACTT[A/G]TGTTTATTTCCTTTT	54778
rs757120601	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59008868	CAAGGAATAATAGAC[A/G]GTTGTATGTATAATA	54778
rs757130780	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59027568	GAGTCTTGCTCTGTT[A/G]CCCAGGCTGGAGTGC	54778
rs757150592	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59000413	CGGCCCATTTTTAAG[A/G]TTATGAAGGACCTCA	54778
rs757189006	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59037784	GAGGTTGCTGTGAGC[C/T]GAGATCACGCCATTG	54778
rs757202645	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59091565	ATTCCATCATATGGC[A/G]GTACTGTAATTTTTT	54778
rs757221605	snp	A/G	1.70426e-05	0.00291908	intron-variant	RNF111	GRCh38.p7	15:59075924	TTGACCAAACTTTAG[A/G]AAGATAAAATATACT	54778
rs757228855	snp	A/G	1.67326e-05	0.00289241	intron-variant	RNF111	GRCh38.p7	15:59052266	TAACGATTAGCTGAC[A/G]GGAAGATGCCTTTAA	54778
rs757245308	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59079165	TGTCTAAAGAGTAGT[G/T]AAATAAATGGACTCA	54778
rs757254181	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59057228	CATCTCCTCCCCAGC[A/G]AACAAAAAATTGTCT	54778
rs757263858	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59080338	GTTGGCCAGGCTGGT[C/T]TCGAACTCCTGGCTT	54778
rs757277657	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59072093	GCTAATACATTTTTT[A/T]AAAATGCCAGCAATC	54778
rs757303468	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59054186	TTGTGATCCACCCGC[C/T]TCGGCCTCCCAAAGT	54778
rs757320391	snp	A/C	1.65061e-05	0.00287277	missense	RNF111	GRCh38.p7	15:59052413	AAGTGGAGATTGTAA[A/C]AGTTGGAGAAAGCTA	54778
rs757340574	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59019244	TATTTATTTTATTAA[A/T]TTAAGTTTTAATTAT	54778
rs757382776	snp	C/T	4.94368e-05	0.00497152	missense	RNF111	GRCh38.p7	15:59076014	GGAAGTGGCAGTTTT[C/T]ATGGAGCATCTGCAT	54778
rs757404265	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59019284	CCACTGAACAAAATA[A/C]TGAGAAAATGCAAAC	54778
rs757455806	in-del	-/TTTTTTTT			intron-variant	RNF111	GRCh38.p7	15:58996652	CATCAGTACTTTCTT[-/TTTTTTTT]TTTTTTTTTTTTTTT	54778
rs757470859	snp	C/T	8.32369e-05	0.0064507	missense	RNF111	GRCh38.p7	15:59055761	CGGCCACAGGAGCCA[C/T]GGAACCGCAGTAGGA	54778
rs757472439	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59028765	AATGCTAGGTCACAT[A/G]GCAATTTTGTGTTTA	54778
rs757473278	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59083252	TGGGATGCAAAATAA[A/T]GAGTATGAATGGAGG	54778
rs757475156	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59071093	ATGAAGTCAGGAGAT[G/T]GAGACCATCCTGGCT	54778
rs757502543	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59003158	TCTCACTCAGTTTCG[C/T]AGGCTGGAGTGCAGT	54778
rs757533113	snp	C/G	1.6477e-05	0.00287024	missense	RNF111	GRCh38.p7	15:59031127	GCCAGCAGGCTGGCC[C/G]TTCGTATGTGCAGAA	54778
rs757544363	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59023779	GTGTTTCACTATTAA[C/T]CATCAGTTTTTTTCC	54778
rs757561873	snp	A/C	1.65201e-05	0.00287398	synonymous-codon	RNF111	GRCh38.p7	15:59058549	TGGCACTTCTATAGG[A/C]GGTATGTAAAAAAGT	54778
rs757566589	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59012927	TATTTTTAGTTGAGA[C/T]GGGGTTTCGCCATGT	54778
rs757587213	in-del	-/TCCT	8.2373e-05	0.00641714	utr-variant-3-prime	RNF111	GRCh38.p7	15:59094940	TCCCTCTCATTCCCA[-/TCCT]TCCTGGTACTGCAGT	54778
rs757595610	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59093486	AAAATGCTGGGATTA[C/T]AGGCGTAAGCCACTG	54778
rs757633872	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59053478	TTTAAAAGTATATAT[C/T]CATATTTCTGACATC	54778
rs757673429	snp	C/G	1.65211e-05	0.00287407	missense	RNF111	GRCh38.p7	15:59031471	TGCAGAAAGAGATTT[C/G]TAAAAAATAATTCCT	54778
rs757681289	snp	A/G	4.94719e-05	0.00497328	missense	RNF111	GRCh38.p7	15:59031553	GAGAAGTGTTAGCTC[A/G]AAGAAAATATGCCTT	54778
rs757689403	in-del	-/GCTCACGCCT			intron-variant	RNF111	GRCh38.p7	15:59078590	AGACCAGGCACAGTG[-/GCTCACGCCT]GTAATCCCAGCACTT	54778
rs757718742	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:58997467	AATCAAGACAGTGGC[C/G]AAACTGCATTAGTAA	54778
rs757731662	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59054428	GTGGACCTATAACTT[C/T]CTTCAGCTATTAACA	54778
rs757755468	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59086089	TGCCGTAAGTGGTAA[C/T]AGATCCGTTCTGATG	54778
rs757766930	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59003421	TTTCTTTTTTGAGAC[-/A]AGAGTCTGGCTCTGT	54778
rs757813513	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59063820	TCAACGTAATCCTCA[A/G]ATAACTTGGTTTGTA	54778
rs757818876	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59023063	ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCTGTC	54778
rs757828089	snp	A/G	1.64895e-05	0.00287132	missense	RNF111	GRCh38.p7	15:59085697	TGACTGCAGCTACTT[A/G]TACACCTGGTGCATT	54778
rs757832322	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59015144	TAGGACCAAAGTCGA[A/G]TTTTTTAAATTCTGA	54778
rs757835033	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59092389	TCACTTAATTCATCC[A/C]TTTATTTATGACAGT	54778
rs757841784	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59057548	TTCCTACCGTTCTCA[A/G]TTTTAAGCAACCATT	54778
rs757850804	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59004925	CTGAGAGACACTTGG[A/G]AAGTGAGACCCAGTG	54778
rs757855516	snp	A/G	1.71997e-05	0.0029325	synonymous-codon	RNF111	GRCh38.p7	15:59080946	TGCAGATGCCTCTTT[A/G]ACAAGGCCACTTCAT	54778
rs757905046	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59002089	CGGTTAAAGCTTGTG[A/T]GCTGTTTATTTCTAG	54778
rs757907083	in-del	-/TT			intron-variant	RNF111	GRCh38.p7	15:59041962	ATCAGTCTGTTCATA[-/TT]TTTTTTTTTTTTTTT	54778
rs757929002	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59016559	TATTTGAATAATTGA[G/T]CATATACCATATTAG	54778
rs757931700	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59044272	CTGACCTCAGGTGAT[C/G]CATCTGCCTTGGCCT	54778
rs757961673	snp	C/T			downstream-variant-500B	RNF111	GRCh38.p7	15:59097591	TAGAGAAAACTACTT[C/T]TGTTTTAAAAACTGT	54778
rs758053200	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59068552	TGGAGGTTGTAGTGA[G/T]CCAAGATCGTGCCAC	54778
rs758098140	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58999192	CATGATAAATGGAAT[A/G]CAGATGCAGATGTGA	54778
rs758101206	snp	A/G	1.64993e-05	0.00287218	missense	RNF111	GRCh38.p7	15:59031577	ATGCCTTGCTACCTA[A/G]TTCTAGTAGTTCCAG	54778
rs758111634	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59056396	GGAAAAGTGGTAGAA[G/T]TTAGGAATATATGAA	54778
rs758130009	snp	G/T	0.000231409	0.0107541	missense	RNF111	GRCh38.p7	15:59067064	CAAATAGTAGTTCTG[G/T]TACCAGCTATCATGA	54778
rs758133036	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59056066	AGCTATTTTCTCAGG[-/A]AAAAAATATTTTTGT	54778
rs758141587	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59048976	TGTGGTGGTGTGCAC[C/T]TGTAGTCCCAGCTAC	54778
rs758155441	snp	A/G	1.66291e-05	0.00288345	missense	RNF111	GRCh38.p7	15:59052428	CAGTTGGAGAAAGCT[A/G]TCGGTGAGATTTTAA	54778
rs758164851	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59009145	TTGTATTTTTAGTAG[A/G]GATGGGGTTTCACCA	54778
rs758168250	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59078972	TGAGTAAATGTTGGA[A/C]TAAAGCATAGTATTA	54778
rs758219591	snp	C/G	1.72472e-05	0.00293654	intron-variant	RNF111	GRCh38.p7	15:59075911	TAACATGAAATATTT[C/G]ACCAAACTTTAGAAA	54778
rs758223190	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58989379	ACAAATGACTTTATC[A/G]TCTCTCTCCTGCTCA	54778
rs758233228	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59061210	ACAAATCAGATTTAA[C/T]TTCTGAGCATCTTGG	54778
rs758272648	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59000321	GGCATGTACCACCAC[A/T]CTTGGCTCATTTTTC	54778
rs758279900	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59077738	ATTGCTATGTCAGAG[A/G]GCTAAACTTTCAGAT	54778
rs758294026	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59037617	CAAGGCAGGTGGATC[A/T]CCTGAGGTCTGGAGT	54778
rs758322787	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59047902	AAATGGTTATTAAAA[A/C]CACAATGAGATACCA	54778
rs758400688	snp	C/G	3.04058e-05	0.00389897	intron-variant	RNF111	GRCh38.p7	15:59092502	TCAATAATGTCATCT[C/G]TACTAATAAGGTAAC	54778
rs758402640	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59089183	TCAGTTCACACATAT[A/G]TAATCCATAAATAAT	54778
rs758421035	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59090036	GTCAGATATATAACT[A/G]TACCATTAAATGTGG	54778
rs758440352	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59040400	TCCTCATTTGCTGCA[A/G]TTACAGGTGTGATGT	54778
rs758445043	in-del	-/TCTTTTTT			intron-variant	RNF111	GRCh38.p7	15:58996648	AACTCATCAGTACTT[-/TCTTTTTT]TTTTTTTTTTTTTTT	54778
rs758457091	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59070125	AGTAATCCTCCTGCC[C/G]CAGACTTCTAATTGG	54778
rs758480558	snp	C/T			utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096131	TATAGTTAAGATTTA[C/T]TGCATAATATAGAAT	54778
rs758490550	snp	A/G	1.64738e-05	0.00286995	missense	RNF111	GRCh38.p7	15:59076089	GGCCATCAGGCCGCT[A/G]CTGCTGCCCCAAGTC	54778
rs758510359	snp	A/C	1.64806e-05	0.00287054	intron-variant	RNF111	GRCh38.p7	15:59094776	TTTGTTTTCTTGCCA[A/C]TAATAGACGTCTTCC	54778
rs758515769	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59052024	AAATATCTATATAAG[A/G]TCTTACAAATCATGT	54778
rs758528945	in-del	-/TG			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986185	TTTTAAAATCATTTG[-/TG]TGTGTGTGTGTGTGT	54778
rs758563011	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58991351	TTACATTTTAAAGAG[C/T]GGTACTGCATTATTA	54778
rs758581563	snp	A/C	1.85029e-05	0.00304157	intron-variant	RNF111	GRCh38.p7	15:59055880	GTAGAAAATTATGAA[A/C]GGAGTTTGATAAAAG	54778
rs758601692	snp	A/G	1.64746e-05	0.00287002	utr-variant-3-prime	RNF111	GRCh38.p7	15:59094933	CTTGCCCTCCCTCTC[A/G]TTCCCATCCTTCCTG	54778
rs758618171	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59003083	CTGCAGCCTTGAACT[C/T]CTGGCCTCAAGTGAT	54778
rs758639991	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59063720	AAATGCTCGAAGGCA[A/G]AAGAGGACAAGCTGT	54778
rs758671490	snp	C/T	1.64776e-05	0.00287028	synonymous-codon	RNF111	GRCh38.p7	15:59058405	GGAATCACAAGCTAC[C/T]AGCGCTTCCATTAAC	54778
rs758702490	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59053325	TAGATGATTATAAGT[A/G]TTGGTAATAATAGCA	54778
rs758705363	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59022996	TTACGCCTGTAATCC[C/T]AGCACTTTGGGAGGC	54778
rs758706850	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59080377	TCTGCCCACCTTGGC[C/T]TCCTAAAGTGCTGGG	54778
rs758742426	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58995522	GGAGTGCAGTGGCGC[A/G]ATCTTGGCTCACTGC	54778
rs758762867	snp	A/T	1.65974e-05	0.0028807	missense	RNF111	GRCh38.p7	15:59031655	GAGAAGAAGATTTGT[A/T]TGTTTCTGCCAGTGA	54778
rs758789788	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59091745	TTGACACCAGGGACC[A/G]GTTTTCATGGAAGAC	54778
rs758823892	snp	C/T	1.64838e-05	0.00287083	synonymous-codon	RNF111	GRCh38.p7	15:59089675	GAAATAGGTTCCTGA[C/T]ATGGCAGGCTATCCT	54778
rs758851181	in-del	-/C			intron-variant	RNF111	GRCh38.p7	15:58990985	ATGAGGAGTGAATTA[-/C]AAATATTTAAAGACA	54778
rs758879788	snp	C/T	1.65811e-05	0.00287929	synonymous-codon	RNF111	GRCh38.p7	15:59085773	CTTACAATTAGGAGC[C/T]CTTCCTTTAATGGTA	54778
rs758889706	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59005838	GCATATGTTACTTTG[C/T]TTAATATTTACAACA	54778
rs758974893	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59074423	TAGCTGGATTTTCTA[C/G]ATAACTTACTGTAGC	54778
rs758996319	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59032929	CAGTAAATGTGATAT[A/T]TAAGTAGAATAAGTT	54778
rs759048789	snp	A/C	4.94197e-05	0.00497066	utr-variant-3-prime	RNF111	GRCh38.p7	15:59094915	ACACCATGTTTCAGA[A/C]CTCTTGCCCTCCCTC	54778
rs759055673	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59009969	AAAAACAAACAAACA[A/G]AAATTAAAATGATTT	54778
rs759062491	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59008898	ATGAGAAACTTAAAA[C/G]AGTATACTTTCATTT	54778
rs759084642	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59037365	GTCAAGAACTCCAGA[C/T]ATTTAAAATAACCTA	54778
rs759109738	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59050501	AAAGTAGACTTACCC[A/T]GACACTAGACTCTAT	54778
rs759134492	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59038572	GAACTCCCATATAAT[C/T]ATCATCTCGCTTCAG	54778
rs759194260	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59072743	AGGCGTGAGCCACCA[C/T]ACCCGGCCTGTCATT	54778
rs759195547	snp	C/T	1.64727e-05	0.00286986	stop-gained	RNF111	GRCh38.p7	15:59066913	CATACAAGTTGCTTT[C/T]AGCAGCATGGTCACC	54778
rs759235837	in-del	-/GAAAGCTAT	1.65329e-05	0.0028751	cds-indel	RNF111	GRCh38.p7	15:59052421	ATTGTAACAGTTGGA[-/GAAAGCTAT]CGGTGAGATTTTAAT	54778
rs759277530	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59061903	TCTGACAATTGTCTC[C/T]TTTTCATAATTCATT	54778
rs759278946	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59062907	AGGATATTTAGCAGC[A/G]TCCTTGGTTTGTAGC	54778
rs759302488	in-del	-/GTTTTGTTTG			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986205	TGTGTGTGTGTGTGT[-/GTTTTGTTTG]TTTGTTTGTTTGTTT	54778
rs759303592	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59090892	TAAACTGTTTTATAT[A/G]TATACTTATATATAA	54778
rs759321368	snp	C/G	1.64749e-05	0.00287005	missense	RNF111	GRCh38.p7	15:59067027	GTGGAAAGACCTCCA[C/G]AAGTACAAGCACCTT	54778
rs759371658	snp	A/G	6.59473e-05	0.00574189	synonymous-codon	RNF111	GRCh38.p7	15:59076148	ATCAAGCATGGTTGC[A/G]CAGCCCCAGCCCCAG	54778
rs759390516	in-del	-/AGT			intron-variant	RNF111	GRCh38.p7	15:58989476	AATATTTTAGGAAAA[-/AGT]AGGAAGAATGAGTCT	54778
rs759423189	snp	A/G			utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096089	ACATTACCAAGAGTC[A/G]ATCACTGATTTAAAA	54778
rs759445446	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59083165	AAAAAGAAGCAAAAA[A/T]TGAATCCCTGAAACT	54778
rs759447701	snp	G/T	1.73634e-05	0.00294642	intron-variant	RNF111	GRCh38.p7	15:59055853	TGAAGATGGTAAATT[G/T]AAGTAGTAACAGTAG	54778
rs759456729	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:58994476	TATTTTCTCTCTCTT[-/T]TTTTTTTTTTTTTTT	54778
rs759475655	snp	A/G	1.81073e-05	0.00300887	missense	RNF111	GRCh38.p7	15:59092567	AAACAAGATGGGGAA[A/G]AAGGGACTGAGGAAG	54778
rs759487125	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59003695	GTGTGAGCCACTGCA[C/T]GTGGCGTATTTTCTT	54778
rs759495185	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59080295	TGGATAATTTTTGTA[-/T]TTTTTAGTGGAGACG	54778
rs759512790	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59003144	TTTTCGAGACAAGGT[C/G]TCACTCAGTTTCGCA	54778
rs759535474	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59084544	TAGTATTTCAATACA[C/T]ACATACATTGTGAAA	54778
rs759537802	snp	C/T	1.64751e-05	0.00287007	missense	RNF111	GRCh38.p7	15:59031243	GATTGTCTTTCTTCT[C/T]CTTCATCTAGTCTGC	54778
rs759542624	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:58993037	TAGCCGGGCATGGTG[G/T]CGGGTGCTTGTAATC	54778
rs759567903	snp	A/G	3.30038e-05	0.00406212	missense	RNF111	GRCh38.p7	15:59080995	CCGCATTCTCATGGA[A/G]ACCCCCCTCCTCAGA	54778
rs759576020	snp	A/G			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986281	GAGTGCAGTGGCACA[A/G]TCTCGCACTCACTAC	54778
rs759639280	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59025164	TGCAGGGATTACAGG[C/T]GTGAGCCACTGCGCC	54778
rs759654142	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58998407	CCTCCTCCCACCCTC[C/T]ACACTCTGAAAGATT	54778
rs759675242	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59022973	GGAAATTGGCTGGGC[A/G]CGGTGGCTTACGCCT	54778
rs759691963	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59066218	CTATTGCCATACTTA[A/C]ACATCACAGTAAATA	54778
rs759697436	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59023624	TTGTCAGTGTCATCT[A/G]CCAATAATGAAAAAA	54778
rs759723062	snp	A/G	1.64741e-05	0.00286998	missense	RNF111	GRCh38.p7	15:59058500	CTTCCACAGTGTCAG[A/G]GACTTCAGCTACTCT	54778
rs759740918	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59075399	TGGCAAAGGTAATTC[A/G]TGATTTAGTCTGAAA	54778
rs759800099	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59016272	CCTCCTGGATTCAAG[C/T]GATTCTCCTGCCTCA	54778
rs759805171	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59086968	AAGAGGTAAATATTG[A/T]TGAATGCCTGAATGA	54778
rs759810930	snp	A/T	1.65897e-05	0.00288003	intron-variant	RNF111	GRCh38.p7	15:59058579	TGGGGGAGGGGAGAC[A/T]TTTTGTCATTACTTT	54778
rs759828226	snp	A/G	1.64795e-05	0.00287045	missense	RNF111	GRCh38.p7	15:59052365	CCCAGGTTACTGCCA[A/G]TGAAGAAATTAATGT	54778
rs759877492	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59058179	AATATTTTGGTAACA[C/T]GTCTGTTCGATATTG	54778
rs759893468	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59072731	TGCTGGGATTACAGG[C/T]GTGAGCCACCACACC	54778
rs759908644	snp	A/G	1.65002e-05	0.00287225	synonymous-codon	RNF111	GRCh38.p7	15:59031530	GATATTAATGCAGAG[A/G]AAGAAACGAGAAGTG	54778
rs759909887	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59049772	TTTTTTTTTGAGATG[C/G]GGTCTCGCTCCGTCA	54778
rs759919601	snp	A/C			intron-variant, utr-variant-5-prime	RNF111	GRCh38.p7	15:58988369	GGGGGCTGAGGACCG[A/C]GGCGTGGGAGTGCGA	54778
rs759920257	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59028160	AGTTGAATCCTCCGA[C/T]GATCCCCAGCCCTAG	54778
rs759923420	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59027255	GAAATCCACCAGAAC[A/G]TAACTCTGACATGGG	54778
rs759935027	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59085990	TGTACTCTTAATGTA[C/T]GACATGACAAAAAAG	54778
rs759961009	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59005451	AGAAATTGTTTCCTT[A/G]GGCAGTTTTGCTCCC	54778
rs759965428	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59044923	TATATAATTTTTATG[A/T]ATTATGTTCAAGTTA	54778
rs759988227	snp	C/G/T	3.47121e-05	0.00416594	intron-variant	RNF111	GRCh38.p7	15:59067119	TCTTTCTTTCCTGCC[C/G/T]CTCTTGTCTCTCTCT	54778
rs759989611	snp	C/T	1.80961e-05	0.00300794	missense	RNF111	GRCh38.p7	15:59030824	CCTTAAAGTTTCCCA[C/T]GTCTCAATGGACTCC	54778
rs760010468	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59017165	CCCCACCCTGGGTCT[G/T]TGGAAAAATTGTCTT	54778
rs760040918	snp	C/G	3.48311e-05	0.00417305	intron-variant	RNF111	GRCh38.p7	15:59052450	AGATTTTAATTCTTA[C/G]TTAAATGTTTGAAAT	54778
rs760050087	snp	A/T	1.70621e-05	0.00292074	missense, intron-variant	RNF111	GRCh38.p7	15:59084107	TTATTTCCAGTGGTC[A/T]TTTTGTGTTCTGTGT	54778
rs760064149	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:58990445	CGGGCGAATCACTTG[A/T]GGTGACCAGTCTGGC	54778
rs760089611	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59069459	ATTAATAAAATAATA[C/T]AGCTAGTTTGAGACA	54778
rs760110284	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59083536	CTAGACTTCCTCTCC[-/A]AAAAAAAAAAAAAGT	54778
rs760124002	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59048554	ACTCCATAAATTTAC[A/T]AAAATTAGCAAAATG	54778
rs760131081	snp	C/T	1.64855e-05	0.00287097	missense	RNF111	GRCh38.p7	15:59030956	CAGAGCCCATTGGGG[C/T]AGCCAAAAGTTTTCC	54778
rs760177150	in-del	-/CTT			intron-variant	RNF111	GRCh38.p7	15:58989871	ATTTTTAGATGTTTC[-/CTT]CTTTTTTTTTTTGTT	54778
rs760210711	snp	C/T			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020332	GCAGTATCTTTATGT[C/T]TTATTTAGTATACAT	54778
rs760228902	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59047781	GTTTTTCGCCATGTT[A/G]CCCAGGCTGGATTGA	54778
rs760255673	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59035983	ATCTTTACAGAATCA[A/C]CCCACTCTGTTAGTA	54778
rs760255937	in-del	-/TTGTATGG			intron-variant	RNF111	GRCh38.p7	15:59034842	TTACTACATGTTAAT[-/TTGTATGG]ATGATTTGTATGGAT	54778
rs760274454	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59010762	TCCCTGCTTGAAGGT[A/C]ATGGAAAAGTTGAGA	54778
rs760295126	snp	C/G	1.64781e-05	0.00287033	missense	RNF111	GRCh38.p7	15:59067036	CCTCCACAAGTACAA[C/G]CACCTTGTGGAGCAA	54778
rs760329344	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59058886	AAGGATATTATCAAG[A/G]CAGTGAAAGACAGCC	54778
rs760329795	snp	A/C/G/T			intron-variant	RNF111	GRCh38.p7	15:59008790	TTTTGGCTTATACTT[A/C/G/T]AAAAAAAATCTTTTG	54778
rs760332493	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59083101	TTACACTGAGCTATG[A/T]TTGTGCCACTGCACT	54778
rs760335178	in-del	-/ATTA			intron-variant	RNF111	GRCh38.p7	15:59049606	ATGCTCATTATATAC[-/ATTA]ATTCTTTTGGCAAGA	54778
rs760339233	snp	C/T			synonymous-codon	RNF111	GRCh38.p7	15:59030948	TTTGCATCCAGAGCC[C/T]ATTGGGGCAGCCAAA	54778
rs760350783	in-del	-/TTAG	1.70803e-05	0.0029223	intron-variant	RNF111	GRCh38.p7	15:59052447	GTGAGATTTTAATTC[-/TTAG]TTAAATGTTTGAAAT	54778
rs760378734	snp	C/T	1.74613e-05	0.00295472	intron-variant	RNF111	GRCh38.p7	15:59067123	TCTTTCCTGCCCCTC[C/T]TGTCTCTCTCTCTCT	54778
rs760379391	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59079877	TGACATGGGGTAGGG[A/G]GAGAGAGAGACAGTT	54778
rs760390333	in-del	-/CTTTT	1.87887e-05	0.00306496	intron-variant	RNF111	GRCh38.p7	15:59085830	ATGTTCTAAAAGTTC[-/CTTTT]CTAAGTATTTTATTG	54778
rs760395750	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59056831	AATTAAATATAGGGT[C/G]ACTATTTTGGAAACT	54778
rs760430972	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:58994173	CTCCCAGGTAGCTGG[G/T]ATTAGAGGTGCACGC	54778
rs760454435	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59060875	GGCACAATCTTGTCT[C/T]ACTGCAATCTCCACC	54778
rs760468869	snp	A/T	2.43561e-05	0.00348962	intron-variant	RNF111	GRCh38.p7	15:59052466	TTAAATGTTTGAAAT[A/T]TTAAATATAAATATT	54778
rs760475584	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59045153	GTGTTCGATAATGTT[A/G]GCTTATTTTTTACAG	54778
rs760530899	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58992155	GTTCAAGCAATTCTT[C/T]TGCGTCAGTCTCCTG	54778
rs760557447	snp	A/G	1.64825e-05	0.00287071	missense	RNF111	GRCh38.p7	15:59031348	AATGCTAAAAGTAGA[A/G]GCCATAGTGCACGGT	54778
rs760581022	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59071800	GCTTTCCCTAAAATC[A/G]TATTCCTAATACAAG	54778
rs760609260	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59093043	GAAACCAAATAAAGA[C/T]TACTTTTGGCATATA	54778
rs760611519	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59012368	CAGTATTTGATAATT[A/C]AGACCCTTAGCCTTT	54778
rs760614378	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59073928	TGTTGTGTTAGGTAT[G/T]AAAACATTAATCTAC	54778
rs760643011	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59005244	GTTGCCTAGGCTGAT[C/T]TCAAACTCCTGGGCA	54778
rs760645483	snp	G/T	1.65105e-05	0.00287315	missense	RNF111	GRCh38.p7	15:59031425	AATGAAAAGACCCTG[G/T]TTACATGGCAGTTCG	54778
rs760648212	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58987676	CTAGTGTCGTGCTCT[C/T]CTCGGTAGGGGAGGA	54778
rs760652452	in-del	-/AAA			intron-variant	RNF111	GRCh38.p7	15:59036719	GAAATGAACTGATGG[-/AAA]AATGTTTTACATTTT	54778
rs760677698	snp	A/G	3.32171e-05	0.00407522	missense	RNF111	GRCh38.p7	15:59066781	GACTCAAGGAGAACT[A/G]CATCTAGTGCTGTAA	54778
rs760718114	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59007441	GTTTGGTATCCCGTT[A/G]TAGCTGTATAACATA	54778
rs760730014	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58995264	TTATTTTGTAACTCA[C/T]CCATTTTCTTCACTA	54778
rs760735039	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59082317	GCTAATCTTTTGTCT[A/G]TGTGTTTCTGCAATA	54778
rs760760608	snp	A/G	1.65441e-05	0.00287607	synonymous-codon	RNF111	GRCh38.p7	15:59031629	ATCCTCTTCTAGCTC[A/G]TCAACTGAAGGAGAA	54778
rs760776174	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59063209	TTATTGAGCCACCTA[C/T]ATTGTGCAAGCATGT	54778
rs760810783	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59041737	GATTGTAACCATTCT[A/G]AATGCTCACCGGCAA	54778
rs760814492	snp	C/G	3.29837e-05	0.00406088	missense	RNF111	GRCh38.p7	15:59031543	AGGAAGAAACGAGAA[C/G]TGTTAGCTCGAAGAA	54778
rs760822438	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59032702	TTTTCTTTAAGTACT[A/G]TATTCTTGTTGTTTG	54778
rs760843722	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59005029	AATCTCCTACATGGT[G/T]TAAATTATTTTTTTC	54778
rs760851137	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59033398	GTTTTACCTACACAA[A/T]TACTTTTTTGAGAAG	54778
rs760854469	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59058016	TCGTGACCATGTGTA[C/T]GTGCATAGTAAGGAA	54778
rs760874984	snp	A/G			synonymous-codon	RNF111	GRCh38.p7	15:59085761	TCGACTTCATCACTT[A/G]CAATTAGGAGCTCTT	54778
rs760906402	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59004463	GGGTAGCACCTTACT[A/G]TCTTTTTATCACCTT	54778
rs760928833	snp	A/G			utr-variant-3-prime	RNF111	GRCh38.p7	15:59097417	CTGATCGTTTGAAAC[A/G]TTTTTCTTACTCTGG	54778
rs760931058	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59084757	CGACCAGCATCTCCC[C/G]TTTCCTCATTCATGA	54778
rs760960463	snp	A/C	1.69238e-05	0.00290888	intron-variant	RNF111	GRCh38.p7	15:59091202	TTACTGAAAGGCATA[A/C]ATGTAATATATACCT	54778
rs761017191	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59044068	AGAGTTTCGCTTTTG[C/G]CGCCCAGGCTGGAGT	54778
rs761031334	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59065538	TTCCCTAAGGTCACA[C/T]TGCTGAAAGAAAGGT	54778
rs761032015	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59027067	TAATTGTGCTGTGAA[C/T]TGCTTCTTTGTAAAT	54778
rs761036102	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59014941	TATTTTTTTAGAGAC[A/G]GAGTTTCACCATGTT	54778
rs761036501	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59068348	ATGGTGGCTCACGCC[G/T]GTAATTCCAGCACTT	54778
rs761046366	snp	G/T	9.67773e-05	0.00695552	intron-variant	RNF111	GRCh38.p7	15:59092646	AAGATGTGAGGTAAC[G/T]AGATATTAATTATCT	54778
rs761093617	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59052792	ATTGTTGCCCAGACT[C/T]TTTCCCATACTTGAA	54778
rs761108433	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58989752	TTTAAGAGAAAAGCA[C/T]CTTGCTTGTATAAAG	54778
rs761126157	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59057257	CTAGCCCAAAATGTT[A/C]GTATTGCCAAGGTTG	54778
rs761126854	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59037237	TTTCTATTATGTGTA[A/G]AAAGCCAAAGTGATA	54778
rs761140500	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58990387	GCTGTGGGCCAGGCG[C/T]GGTGGCTCACCCCTG	54778
rs761145093	snp	C/G	0.00047111	0.0153406	intron-variant	RNF111	GRCh38.p7	15:59067122	TTCTTTCCTGCCCCT[C/G]TTGTCTCTCTCTCTC	54778
rs761194628	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58991418	ACAGTCACTGGTCTT[C/T]AGTGAAGGCACTCTG	54778
rs761195027	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58999746	ATAACTGAGACTGGG[C/T]AATTTATAAAGAAAA	54778
rs761202158	snp	A/G	1.64838e-05	0.00287083	missense	RNF111	GRCh38.p7	15:59031060	GAGAAGGAAATGAAT[A/G]GTAACCAGCAAGAAC	54778
rs761206935	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59009836	TGGCTCATGTCTCTA[C/G]TCCCAGTTACCTGGG	54778
rs761232170	snp	C/T	1.64738e-05	0.00286995	synonymous-codon	RNF111	GRCh38.p7	15:59081156	ACCAATCCCTCAGCA[C/T]CTTCCTCCTACACAC	54778
rs761284498	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59015883	ATTTATTCGAGACAG[G/T]TTCTCACGCCCAGGT	54778
rs761324676	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59071817	ATTCCTAATACAAGC[A/G]TACCTTGGAGATACT	54778
rs761329469	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59028247	ATCTTACATTATGTT[A/G]TCTTTTTGACTGGTT	54778
rs761338299	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59046408	ATGTTACCCAGGCTG[G/T]TCTCGCACTCCTGGG	54778
rs761350899	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:58992738	GGTGAGAGGATGGCT[A/T]GAGCCCGGGAGGCAG	54778
rs761363239	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59029097	TATTTAATTTTTGAG[A/G]ATCTGCTAGACCGCT	54778
rs761399384	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59002755	CTGACTACTTCTGAT[A/G]TCATTGTGTGCCATT	54778
rs761412182	snp	A/G	3.31994e-05	0.00407414	intron-variant	RNF111	GRCh38.p7	15:59055631	TGGGTTTTTGTGGTG[A/G]CTAAAAATTCTTTAT	54778
rs761468608	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59068297	CATATACTATTCCAG[-/A]AAAAAAGTGCTGCAA	54778
rs761474839	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58991863	CAAACCAATTGTAGA[A/G]AGTCATTTTTGAAAC	54778
rs761486112	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59041178	CATACTCCCTTGCAT[A/G]GTTGTACCAGTTTGT	54778
rs761490509	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59092867	TATTTGCATGTGATG[A/G]TGTGCACCTGCAGTG	54778
rs761526904	snp	A/T	2.98512e-05	0.00386325	intron-variant	RNF111	GRCh38.p7	15:59092671	TTATCTAAAATCCAT[A/T]GTCAAAACTGTACAT	54778
rs761528145	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59082085	CCTGTCTCTCCCCCT[A/C]TCCCCAAAAAAGTAA	54778
rs761579623	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59059271	CTCAACATCACTAAT[C/T]ATTAGGGAAATGCAA	54778
rs761584545	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59012282	CCTAGGCCTCCCAAA[A/G]TGTTGAGATTACAGG	54778
rs761586086	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59070766	TTTCTATTATTCCCC[C/T]TAAACCTAGAGCTCA	54778
rs761620305	in-del	-/TATC			intron-variant	RNF111	GRCh38.p7	15:59052012	ATATTACAGGATAAA[-/TATC]TATATAAGATCTTAC	54778
rs761625836	in-del	-/G	1.67922e-05	0.00289755	intron-variant	RNF111	GRCh38.p7	15:59091196	GGAGTGTTACTGAAA[-/G]GCATAAATGTAATAT	54778
rs761649614	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59011482	GCTGCGGTAATGAAA[C/T]GCCACAGATGGAGTG	54778
rs761671827	in-del	-/ATT			intron-variant	RNF111	GRCh38.p7	15:59026001	GCCCAAAGTGCTGGG[-/ATT]ACAGGCGTGAGCCAC	54778
rs761680125	snp	A/G/T	3.30274e-05	0.0040636	missense	RNF111	GRCh38.p7	15:59031435	CCCTGTTTACATGGC[A/G/T]GTTCGTTACGGAGAC	54778
rs761766116	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58997966	CTGGAGTGCAGTGGG[A/G]CGATCCTGGCTCACT	54778
rs761788252	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59064274	GGCGTGGTGCCTCAC[A/G]CCTGTAATCCCAGCA	54778
rs761791269	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59042448	TTTTTCACAAGTCAT[A/G]TTTATCAACTTTTAT	54778
rs761807787	snp	A/T	3.37576e-05	0.00410824	intron-variant	RNF111	GRCh38.p7	15:59031708	GTTCCCTCAGGTAAA[A/T]ATGTTTAAGCTGAGT	54778
rs761832848	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59084670	AAACGGTACGTTATT[C/T]TTCACTGTAGTCACC	54778
rs761852527	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59004353	TGCAAAAAAGTATAT[A/T]GGTAAATGTGTGTAG	54778
rs761870404	in-del	-/GCAATAGTACCACTG	1.64773e-05	0.00287026	cds-indel	RNF111	GRCh38.p7	15:59058521	CAGCTACTCTTACAA[-/GCAATAGTACCACTG]GCACTTCTATAGGAG	54778
rs761873361	snp	A/G			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986120	GAAAATCCTAGTCGA[A/G]TGCTCTTTTAGTTTT	54778
rs761908151	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59091934	CTGCTGCTGATCTGA[A/C]AGGAGGAAGAGCTCC	54778
rs761913636	snp	C/T	0.000115316	0.00759243	synonymous-codon	RNF111	GRCh38.p7	15:59076085	CTTTGGCCATCAGGC[C/T]GCTGCTGCTGCCCCA	54778
rs761960029	snp	A/T			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986072	GTCCGGGCAAAATTC[A/T]ATGTTTAAGAGTGAG	54778
rs761962474	in-del	-/AAC			intron-variant	RNF111	GRCh38.p7	15:59078245	TACATTTATATGTAT[-/AAC]AACAATACTTGTGGA	54778
rs761964275	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59043648	CTACAGTGAACATTT[A/G]GGTACAAATCTTTGT	54778
rs761973886	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59026069	CTTATTTCTTTAGAG[A/T]CATGTAAGCAATCAT	54778
rs761996155	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59047568	ATTAGTTATTTTGTG[-/T]TTTTTTTTAATTATT	54778
rs762007880	snp	A/G			utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096273	TGTTTAAATATGCTT[A/G]ATATGCCCCAGATTG	54778
rs762010431	snp	A/C	1.64925e-05	0.00287158	intron-variant	RNF111	GRCh38.p7	15:59089661	CTATCTCTTCTGTTG[A/C]AATAGGTTCCTGATA	54778
rs762030192	snp	A/G	4.96627e-05	0.00498286	intron-variant	RNF111	GRCh38.p7	15:59094736	TGTTAACTACGTACA[A/G]TTATCATAAAATTAA	54778
rs762038159	snp	A/G	3.29516e-05	0.00405891	utr-variant-3-prime	RNF111	GRCh38.p7	15:59094949	TTCCCATCCTTCCTG[A/G]TACTGCAGTCAACCA	54778
rs762042032	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59013812	TTTTTTTTGGAGACA[A/G]GAGTCTCACTCTGTT	54778
rs762047849	in-del	-/GCGGCGGCGGCGGCGAA			utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58987701	GGAGGAATTGGTTAG[-/GCGGCGGCGGCGGCGAA]GCGGCGGCGGCGGCT	54778
rs762057129	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58998665	ATAAATGAAGTGAGC[C/T]GTTCACTTCAAGAAA	54778
rs762100202	snp	C/G	4.96553e-05	0.00498249	intron-variant	RNF111	GRCh38.p7	15:59089806	ACAGTATCTTTAATG[C/G]AGATTGAGTATATAT	54778
rs762150356	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59035520	ATTCCACATAACTTA[G/T]GCAAATTTCTGAGCT	54778
rs762182425	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59078242	AAGTACATTTATATG[C/T]ATAACAACAATACTT	54778
rs762209145	in-del	-/AG			intron-variant	RNF111	GRCh38.p7	15:59031962	TTTTTTTTCTGAAAC[-/AG]AGTCTCACTTTGTCA	54778
rs762226141	in-del	-/TGT			intron-variant	RNF111	GRCh38.p7	15:59007840	TTTTTTGTGGGGTTG[-/TGT]TGTTATTAGAATATA	54778
rs762241456	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59008509	CAGGCGTGAGCCACC[A/G]CACTCAGCCTACCAC	54778
rs762241914	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59025389	CATAGTGATACTTTT[G/T]AGGGAAAATACCTTT	54778
rs762251507	snp	C/G	1.64749e-05	0.00287005	missense	RNF111	GRCh38.p7	15:59031190	TGAGGCAACACCTAG[C/G]GACACCAAGTGATGA	54778
rs762281410	snp	G/T	1.65548e-05	0.002877	missense	RNF111	GRCh38.p7	15:59066789	GAGAACTACATCTAG[G/T]GCTGTAACGGAAACT	54778
rs762356342	snp	A/G	1.65083e-05	0.00287296	synonymous-codon	RNF111	GRCh38.p7	15:59081261	GATGGAAGTTCAAAG[A/G]AGGAGGATGATGCAG	54778
rs762360121	in-del	-/G			intron-variant	RNF111	GRCh38.p7	15:59045380	ATTTTTAGTAGAGAC[-/G]GGGTTTTACCATGTT	54778
rs762370942	snp	A/G	1.6473e-05	0.00286988	missense	RNF111	GRCh38.p7	15:59066881	CGTCACAGAACCACC[A/G]TGCATTAGGACATCC	54778
rs762494036	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59002625	GATCCAGGCTTTGCT[A/C]TCAGGTCTTAGGCAA	54778
rs762530585	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59011172	AAATAGGGTAATTGG[A/G]TCTCTGTTCTTCGAA	54778
rs762532189	snp	C/T	3.35379e-05	0.00409485	synonymous-codon	RNF111	GRCh38.p7	15:59055832	AGTTGTGGACCTTAC[C/T]GTTGATGAAGATGGT	54778
rs762535891	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59027390	CACTTTTTTTAAACC[G/T]CTTGACTTTCTGGCA	54778
rs762553986	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59028199	ATTCTATCTATGTAG[A/T]TTTGCCTATTCCAGA	54778
rs762555811	snp	C/T	1.64811e-05	0.00287059	synonymous-codon	RNF111	GRCh38.p7	15:59031330	CATTCCCAGACCATT[C/T]TGAATGCTAAAAGTA	54778
rs762566882	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58991038	CGCTTGCTCATACCT[A/G]TAATCCCAGCACTTT	54778
rs762571244	snp	C/G	0.00010039	0.00708413	missense	RNF111	GRCh38.p7	15:59081276	GAGGAGGATGATGCA[C/G]CATCCAACGTATGTT	54778
rs762622020	snp	C/G	1.64743e-05	0.00287	missense	RNF111	GRCh38.p7	15:59031207	ACACCAAGTGATGAA[C/G]ATAATGATTCCTCTT	54778
rs762628408	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59016442	TTATTTATATTCTGT[A/T]ATTCTTTCCATCATC	54778
rs762647490	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59091905	AGGGTTCACGCTTCT[A/G]TGAGAATCTATCGCT	54778
rs762664082	snp	G/T	1.64738e-05	0.00286995	utr-variant-3-prime	RNF111	GRCh38.p7	15:59094909	AAGTTGACACCATGT[G/T]TCAGAACTCTTGCCC	54778
rs762673433	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59013768	TTTATTTATATCAGT[A/G]TGGATTCATGGATAT	54778
rs762695440	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59001961	TATTTAATAAAAATT[G/T]TGTGAATGTCATCTC	54778
rs762731370	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59038823	GTGTGCTTTCTGTTG[C/T]GTCACAAATTGAGCT	54778
rs762732078	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59064979	ATTATTTAAGCTGTT[C/T]TGGTTGGATTTTTAT	54778
rs762732684	snp	A/G			synonymous-codon	RNF111	GRCh38.p7	15:59081234	ACTGCATCCTCATGA[A/G]GTGATGCAGAGGATG	54778
rs762777243	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59017753	TTATTTGTTGAACTC[-/T]TTTTTTTTTTTTTTT	54778
rs762799605	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59010258	TTTGAAATTAATAAA[C/T]CCATGACATGTAAAT	54778
rs762844279	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59072794	TTTACCTGGAGAAGA[C/T]TCTATCTCAAGAAAC	54778
rs762846521	snp	A/T	7.30487e-05	0.0060431	intron-variant	RNF111	GRCh38.p7	15:59085823	TTTTGACATGTTCTA[A/T]AAGTTCCTTTTCTAA	54778
rs762855221	snp	A/G	3.30338e-05	0.00406397	missense	RNF111	GRCh38.p7	15:59031612	AATGACCTCAGCAGT[A/G]AATCCTCTTCTAGCT	54778
rs762872413	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59054128	ATTTTTAGTAGAGAC[A/G]GGGTTTCAGCATATT	54778
rs762902344	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59041963	TCAGTCTGTTCATAT[-/T]TTTTTTTTTTTTTTT	54778
rs762906727	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59032659	CTCCTTAGCTCAGGC[A/G]ATCCACCTGCCTTGG	54778
rs762926503	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59062206	CTCTACCACACCTGG[A/C]CAATTTATGTATTTT	54778
rs762930081	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58994398	TTAAAAAATAGTACT[A/G]AGAACTCTTGAATAC	54778
rs762937096	snp	A/G	1.64768e-05	0.00287021	missense	RNF111	GRCh38.p7	15:59076060	CTGTTTCTTCCTCCC[A/G]AGCTGCAATCTTTGG	54778
rs763002710	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59061970	TAGCCCATTTCATAA[C/G]TGTAAGTGTTGTCAC	54778
rs763022044	in-del	-/CTAA			intron-variant	RNF111	GRCh38.p7	15:59044609	AAAGCTATAAACAAC[-/CTAA]CTAACCTTAAAAAAA	54778
rs763033510	snp	C/T	1.66261e-05	0.00288319	intron-variant	RNF111	GRCh38.p7	15:59091022	TCAAGGAATAATCAT[C/T]TTGGCTTTTACCAGT	54778
rs763056586	snp	G/T			stop-gained	RNF111	GRCh38.p7	15:59066799	TCTAGTGCTGTAACG[G/T]AAACTGGCCCTCCTG	54778
rs763071861	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:58989203	GTAAAAATCTTCATG[A/T]CAGTATAAGCCACAT	54778
rs763151407	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59024886	TCTGTCTATGAATTT[G/T]ACTACTCTGGGTAAT	54778
rs763155391	in-del	-/TTTA			intron-variant	RNF111	GRCh38.p7	15:59036071	GTAATTTATTCTATT[-/TTTA]TTTATTTATTATTTT	54778
rs763195748	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59006698	AAGTTACAAAAATAA[A/G]AAAAATAAAGTTACA	54778
rs763243381	snp	C/G	6.65879e-05	0.00576971	intron-variant	RNF111	GRCh38.p7	15:59076247	TGGACACAAAATCTA[C/G]AGTCATGTCAATGAA	54778
rs763307782	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59046302	GGGCTAAGGTGATCC[A/T]CCCACGTCAGCCTCC	54778
rs763319218	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59017234	CGCTGCTGTGTAGGC[A/C]ACGATAATTTTTATT	54778
rs763321503	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59066319	ATATGTTAAGAATAT[G/T]GCACTATCAGCCGGG	54778
rs763333658	snp	C/T	1.64732e-05	0.0028699	missense	RNF111	GRCh38.p7	15:59058491	GTAGCCAACCTTCCA[C/T]AGTGTCAGAGACTTC	54778
rs763341178	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59018057	AGGCACCACGCCCGG[A/C]CTATTTGTTGAGCTC	54778
rs763356571	snp	A/G	3.35486e-05	0.00409551	intron-variant	RNF111	GRCh38.p7	15:59075935	TTAGAAAGATAAAAT[A/G]TACTTCCTTTTTATC	54778
rs763363465	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59069567	AAATAAATATAACTC[A/G]TTTACCCACCTGTAA	54778
rs763372168	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59087121	TAGGAAGTTAAGCCT[A/G]TGGTCTGGATTTCCA	54778
rs763377245	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58997384	TGTAACTGATGTGAA[C/T]ACCAGTTGACATTTG	54778
rs763386018	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59034492	ATGTGTATTCTCATT[A/G]AATCCTTCCAGTACT	54778
rs763399579	snp	A/G	1.70904e-05	0.00292316	intron-variant	RNF111	GRCh38.p7	15:59031729	TAAGCTGAGTAAAAC[A/G]TGGAACCTATTGCAT	54778
rs763430918	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59007351	ATACTTTGTGTCTAG[G/T]TTTCCCTTAGCATGA	54778
rs763443338	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58987958	GGCCGACGTCTGAGG[C/T]GCAGATCGCTGGCTC	54778
rs763453913	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59016567	TAATTGAGCATATAC[C/G]ATATTAGTCAACATT	54778
rs763458060	snp	C/T			utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096236	CAAGATACTTTCATA[C/T]ACAGGATAGCCTAAT	54778
rs763466124	snp	C/G			downstream-variant-500B	RNF111	GRCh38.p7	15:59097603	CTTTTGTTTTAAAAA[C/G]TGTTACTTGTTCACG	54778
rs763496334	snp	A/G	0.000214131	0.010345	synonymous-codon	RNF111	GRCh38.p7	15:59067014	TCCTGCTTGCCCTGT[A/G]GAAAGACCTCCACAA	54778
rs763497185	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59045436	CCTTGTGATCTGCCC[A/G]TCTTAGCCTCCCAAA	54778
rs763499535	in-del	-/ACTC			intron-variant	RNF111	GRCh38.p7	15:59094214	CGTGAAAAAAGTATT[-/ACTC]ACCTTTAATCAGTTA	54778
rs763511141	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58991045	TCATACCTGTAATCC[C/T]AGCACTTTGGGAAGC	54778
rs763518156	in-del	-/TTTGTTT			intron-variant	RNF111	GRCh38.p7	15:58997904	TTGTTTTTCTTTTTG[-/TTTGTTT]TTTGTTTTTTTTGAA	54778
rs763518229	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59034498	ATTCTCATTGAATCC[-/T]TCCAGTACTCTTATG	54778
rs763521728	snp	C/G	1.64798e-05	0.00287047	missense	RNF111	GRCh38.p7	15:59052334	GATGTTGTGGTGATA[C/G]AAGCTTCCTCCACTC	54778
rs763550088	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59067125	TTTCCTGCCCCTCTT[A/G]TCTCTCTCTCTCTCT	54778
rs763631645	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59058557	CTATAGGAGGTATGT[A/T]AAAAAGTGGGGGAGG	54778
rs763640290	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59028216	TTGCCTATTCCAGAC[A/G]TTCCATATAAAGGGA	54778
rs763652520	snp	C/T	1.648e-05	0.0028705	synonymous-codon	RNF111	GRCh38.p7	15:59067041	ACAAGTACAAGCACC[C/T]TGTGGAGCAAATAGT	54778
rs763665306	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59094655	TAATTTAATCGATGT[G/T]TTTTTTATAGAAGAG	54778
rs763718234	in-del	-/TGT			intron-variant	RNF111	GRCh38.p7	15:58988805	GGGGTGACTCCATTG[-/TGT]TGTTGTAAGCTTTCC	54778
rs763719991	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59013126	GCTCCATAGTCACTC[A/G]TTTCTCTCCTGCCTT	54778
rs763735344	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59068608	AAGACTCCGAAGTTC[A/G]TTTTTTTTTCTTTTT	54778
rs763738744	snp	A/G	3.29652e-05	0.00405974	missense	RNF111	GRCh38.p7	15:59052388	ATTAATGTTACCTCA[A/G]CTGACAGTGAAGTGG	54778
rs763755554	snp	C/G	3.29603e-05	0.00405944	missense	RNF111	GRCh38.p7	15:59058397	GCAAGAATGGAATCA[C/G]AAGCTACTAGCGCTT	54778
rs763763519	snp	C/G	1.64738e-05	0.00286995	utr-variant-3-prime	RNF111	GRCh38.p7	15:59094926	CAGAACTCTTGCCCT[C/G]CCTCTCATTCCCATC	54778
rs763776568	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59038848	TGAGCTTGATCAGAG[A/G]GTTCAGATGTTGTCA	54778
rs763808491	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59010261	GAAATTAATAAACCC[A/G]TGACATGTAAATATA	54778
rs763818758	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59032724	TGTTGTTTGCTGTTA[A/T]CATGTTCTTTATAGC	54778
rs763824723	snp	G/T	2.43549e-05	0.00348954	intron-variant	RNF111	GRCh38.p7	15:59052467	TAAATGTTTGAAATA[G/T]TAAATATAAATATTA	54778
rs763856077	snp	A/G	2.2183e-05	0.00333032	intron-variant	RNF111	GRCh38.p7	15:59081311	GTTTTTAAAAAGAAA[A/G]TCAAGTTTGCTTTTT	54778
rs763889610	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58997437	GGTGCATTAAACTAA[C/T]GGCCCTGTAGCACAA	54778
rs763895659	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59011246	CTACCCTTCAGAATC[A/G]GATTAGATTCTACTT	54778
rs763906892	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59008585	GTTGGAAAATCATTT[C/G]ATGATATATTTAAGT	54778
rs763912382	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59050711	TACAATCAGTGCCAT[C/G]GACTTAAATCCATCA	54778
rs763914165	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59056899	AGGAGAAGGTGATAG[A/G]GTAGCCTTTTCCACA	54778
rs763937704	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59062129	GCTCACTGCAGCCTC[C/T]ACTTCCAGGCTTAAG	54778
rs763955278	in-del	-/AGCAGGC	1.64735e-05	0.00286993	frameshift-variant	RNF111	GRCh38.p7	15:59058443	ATCCATCTACCTCTG[-/AGCAGGC]CTCTGATACTGCTTC	54778
rs763956210	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59049035	GAGCCCAGGAGATTG[A/G]CGGCATGAGCGTGAT	54778
rs763975045	in-del	-/AGA			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986699	TTGTATTTTTAGTGG[-/AGA]AGAAGGAGTTTCACC	54778
rs763994766	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59091906	GGGTTCACGCTTCTA[C/T]GAGAATCTATCGCTG	54778
rs764019998	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59079948	TATGCAAATAATACT[C/T]ACAAGTCAATAAGAA	54778
rs764036455	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59063053	TGTTCTAATACTGGT[C/T]GATTTGTATCCTAAA	54778
rs764042265	snp	G/T	1.64917e-05	0.00287151	synonymous-codon	RNF111	GRCh38.p7	15:59031551	ACGAGAAGTGTTAGC[G/T]CGAAGAAAATATGCC	54778
rs764044167	snp	C/T			missense	RNF111	GRCh38.p7	15:59055737	CAGGGTTCCAGTTCT[C/T]ATGCAAGTCGGCCAC	54778
rs764084232	snp	A/G	3.30251e-05	0.00406343	missense	RNF111	GRCh38.p7	15:59031430	AAAGACCCTGTTTAC[A/G]TGGCAGTTCGTTACG	54778
rs764102234	snp	C/T	3.35593e-05	0.00409616	synonymous-codon, intron-variant	RNF111	GRCh38.p7	15:59084117	TGGTCTTTTTGTGTT[C/T]TGTGTTTCCAGGCGG	54778
rs764120999	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59094578	AGATTTTATATAATT[C/T]GGTCCTGTAGCTTTG	54778
rs764158666	snp	A/G			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021196	TGCTCTGTTGCCCAG[A/G]ATGGAGTGCAGTGAT	54778
rs764168277	in-del	-/TTTTTTTTTTTAAGTGTTTCCTCTT			intron-variant	RNF111	GRCh38.p7	15:59045169	GCTTATTTTTTACAG[-/TTTTTTTTTTTAAGTGTTTCCTCTT]TTTTTTTTTTTTGAG	54778
rs764172336	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:58995179	ATCCCCCAAGGCCCA[G/T]GTAGCATCCATTGAT	54778
rs764199938	in-del	-/AA			intron-variant	RNF111	GRCh38.p7	15:59069416	CATTAAAGAGCTGCC[-/AA]AAGTCTCATTTACAG	54778
rs764201197	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59003133	TCTTTTTTCTTTTTT[C/G]GAGACAAGGTCTCAC	54778
rs764201246	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59013604	TGATCAATTGTGATC[A/C]GCTGGCTGAGTAGTG	54778
rs764213013	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59083204	TTTAGTGTCTTCTGT[C/T]AACTGACTTTAGGAA	54778
rs764281434	snp	A/G	6.62592e-05	0.00575545	missense	RNF111	GRCh38.p7	15:59031637	CTAGCTCATCAACTG[A/G]AGGAGAAGAAGATTT	54778
rs764293767	snp	G/T	1.65083e-05	0.00287296	missense	RNF111	GRCh38.p7	15:59085751	ACGCACCTCCTCGAC[G/T]TCATCACTTACAATT	54778
rs764312611	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59034615	AACTGAAATATTAAT[A/G]AGACTTAGCTCTATT	54778
rs764331037	in-del	-/G	0.000273038	0.0116809	intron-variant	RNF111	GRCh38.p7	15:59093500	CAGGCGTAAGCCACT[-/G]GCACTCGGCTATAGC	54778
rs764374355	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59003657	TCTGCCTGCCTCAGC[C/T]TCCCAAACTGCTGGA	54778
rs764376091	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59028136	AACTCCATGCTTTTC[A/G]GCCATCATAGTTGAA	54778
rs764385456	snp	A/G	3.29614e-05	0.00405951	missense	RNF111	GRCh38.p7	15:59076009	GTCATGGAAGTGGCA[A/G]TTTTCATGGAGCATC	54778
rs764386410	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59023641	CAATAATGAAAAAAA[-/T]TACCTTCTTTTAAAT	54778
rs764403315	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59065675	TCTAATCATTTCTTA[C/T]ATTCTATTGGTTCTG	54778
rs764410440	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59088254	AGGATTGAGTTCGAA[G/T]AGGAGAAAAGCTCAT	54778
rs764416975	snp	A/G	5.21839e-05	0.00510776	intron-variant	RNF111	GRCh38.p7	15:59092655	GGTAACTAGATATTA[A/G]TTATCTAAAATCCAT	54778
rs764421652	in-del	-/TT			intron-variant	RNF111	GRCh38.p7	15:59067199	CTCTCCCTCCCTCCA[-/TT]TCTCTCCCTGCTTTC	54778
rs764423284	snp	C/T	1.79748e-05	0.00299784	intron-variant	RNF111	GRCh38.p7	15:59080895	ATATATGTTCAACTG[C/T]ATGGTGCCTATGTAA	54778
rs764430519	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59025187	ACTGCGCCCAGGCAG[A/G]AATCAAGTTTATCTT	54778
rs764466782	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59012664	TCAGTGTATACAGAT[A/G]TATGTCTTGCTATCC	54778
rs764508366	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58997402	CAGTTGACATTTGCA[C/T]TGATGGTGCAAAAAA	54778
rs764510186	in-del	-/CTC			intron-variant	RNF111	GRCh38.p7	15:59033250	GTGCCATTTCTTCTT[-/CTC]TTCTTCTTCTTTATG	54778
rs764525130	snp	A/G	1.66338e-05	0.00288386	intron-variant	RNF111	GRCh38.p7	15:59058590	AGACTTTTTGTCATT[A/G]CTTTCGTTAGGAAAA	54778
rs764573316	snp	C/G	1.64827e-05	0.00287073	missense	RNF111	GRCh38.p7	15:59031065	GGAAATGAATGGTAA[C/G]CAGCAAGAACAAGAA	54778
rs764593045	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59046310	GTGATCCTCCCACGT[C/T]AGCCTCCTGGGTAGC	54778
rs764602193	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59087140	TCTGGATTTCCAAAG[A/G]TATTTGGGTTAAAGA	54778
rs764626888	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59050168	CTCCTGAGTTCCAGC[A/G]ATTTTCCTGCCTCAG	54778
rs764641512	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59000997	GTGGGGTTAACTTTT[A/T]ATTTTTTTGCCTTTC	54778
rs764670956	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59033912	GTTTTCTGGTTTCTG[A/G]ACAAGTGATTTGCTT	54778
rs764700130	snp	A/C	1.66746e-05	0.00288739	missense	RNF111	GRCh38.p7	15:59055735	GCCAGGGTTCCAGTT[A/C]TCATGCAAGTCGGCC	54778
rs764772399	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59068498	GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	54778
rs764779374	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58990448	GCGAATCACTTGAGG[C/T]GACCAGTCTGGCCAA	54778
rs764785441	in-del	-/TTTTTTTTTT			intron-variant	RNF111	GRCh38.p7	15:58996650	CTCATCAGTACTTTC[-/TTTTTTTTTT]TTTTTTTTTTTTTTT	54778
rs764786380	snp	A/G	8.32092e-05	0.00644963	intron-variant	RNF111	GRCh38.p7	15:59091009	TTGACAGTTCTGTTC[A/G]AGGAATAATCATCTT	54778
rs764838039	in-del	-/T			utr-variant-3-prime	RNF111	GRCh38.p7	15:59095731	GTACATACTTGCAGA[-/T]TTAACAAAATTTTAG	54778
rs764885799	snp	A/G	1.64866e-05	0.00287106	missense	RNF111	GRCh38.p7	15:59031003	ATTAATAGTAAAGTG[A/G]GGAATGAATTCTCTC	54778
rs764917524	in-del	-/ATTC			intron-variant	RNF111	GRCh38.p7	15:59011376	CTGGTCTGTGTCTTT[-/ATTC]ATTCATTCTTGTGTT	54778
rs764950214	snp	C/T	1.65477e-05	0.00287638	intron-variant	RNF111	GRCh38.p7	15:59094740	AACTACGTACAATTA[C/T]CATAAAATTAATTTT	54778
rs764974081	snp	A/G	1.64811e-05	0.00287059	synonymous-codon	RNF111	GRCh38.p7	15:59031083	GCAAGAACAAGAAAA[A/G]AGTCTCGTTGTGAGG	54778
rs764981471	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:58999996	ACCATTAGAAATTGC[A/C]CAGATAATCCAGTCA	54778
rs764992385	snp	A/T	1.65037e-05	0.00287256	missense	RNF111	GRCh38.p7	15:59084179	GGATGCACCCAAACT[A/T]TGGTCATGGGCATCA	54778
rs765058675	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59042368	CTGAGCTCAAGTGAT[C/G]CACCCGCTCGGCCTC	54778
rs765082388	snp	C/T	1.65121e-05	0.00287329	intron-variant	RNF111	GRCh38.p7	15:59085649	TAAACTGTTCTCATC[C/T]TTTCGTTAGGGAACT	54778
rs765107801	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59061139	TTTATGTGATACAGT[A/C]CCAACTTTATTTCAG	54778
rs765109145	in-del	-/ATTA	7.45851e-05	0.00610631	intron-variant	RNF111	GRCh38.p7	15:59092651	GTGAGGTAACTAGAT[-/ATTA]ATTATCTAAAATCCA	54778
rs765110340	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59008995	GACAGAGTCCCATTC[C/T]GTCACCCAGGCTGGA	54778
rs765138092	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:58993144	CACTGCCCTTCAGTC[G/T]GGGTGACAGAGCAAG	54778
rs765139820	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59029840	TTTTTAGTGTTCATT[C/T]ATCTATAAACTTAGA	54778
rs765172250	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59059414	ATTGCTGGTAGGAAT[A/G]CAAAATGGTGCAACT	54778
rs765229833	snp	A/T	1.69103e-05	0.00290773	intron-variant	RNF111	GRCh38.p7	15:59031710	TCCCTCAGGTAAAAA[A/T]GTTTAAGCTGAGTAA	54778
rs765232922	snp	A/T	1.77704e-05	0.00298075	intron-variant	RNF111	GRCh38.p7	15:59067130	TGCCCCTCTTGTCTC[A/T]CTCTCTCTCTCCTTC	54778
rs765241118	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59072747	GTGAGCCACCACACC[C/T]GGCCTGTCATTTCCA	54778
rs765246636	snp	C/G			utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58987700	GGGAGGAATTGGTTA[C/G]GCGGCGGCGGCGGCG	54778
rs765307963	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59063477	TTGTGGAGTTAATTT[C/T]CCTAATGCAGGTTCA	54778
rs765316823	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59092078	GAAAATTACTATTCT[C/T]TGTATTTTTCATCTA	54778
rs765353728	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59023657	TACCTTCTTTTAAAT[A/G]TATATGCCCATTCCC	54778
rs765358737	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59033716	ATATAGCCTCAAGTA[C/T]TAAAGAGAAGTCCAA	54778
rs765377875	snp	G/T	0.000509554	0.0159536	intron-variant, utr-variant-5-prime	RNF111	GRCh38.p7	15:59004083	ATCTTTTTGAAACCC[G/T]CTTCCCAGACTCTTG	54778
rs765464476	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59007876	TTTTTATATTCAGTA[C/T]TCAAGTTACGTATAT	54778
rs765466790	in-del	-/AATAA			intron-variant	RNF111	GRCh38.p7	15:59069447	GAATATTTTGTTATT[-/AATAA]AATAATACAGCTAGT	54778
rs765476451	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59045124	TTCAAAATGTTACAT[A/G]AGCCATGTAAAAGGT	54778
rs765485408	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59075762	GTTTTCACAATCCAG[A/G]ATACACTTGTTATAT	54778
rs765516965	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59064764	GGAAAAAACGAATAT[A/G]CAGAAATTTAGATTA	54778
rs765520218	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59005749	AAGAAGCTTGTGGAC[A/G]TCTTTGCCTGGACGA	54778
rs765534518	snp	A/C/G	0.000116803	0.00764127	intron-variant	RNF111	GRCh38.p7	15:59058596	TTTGTCATTACTTTC[A/C/G]TTAGGAAAAGTATTA	54778
rs765567134	snp	C/T	4.94548e-05	0.00497242	missense	RNF111	GRCh38.p7	15:59076171	AGCCCCAGCCCCCTC[C/T]ACAGCCCTCTCTCTC	54778
rs765584538	snp	A/T	1.64743e-05	0.00287	synonymous-codon	RNF111	GRCh38.p7	15:59081177	TCCTACACACCAGCC[A/T]ATTTCGCACCATATT	54778
rs765612397	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59006624	GCTTTACATTTCTAG[C/T]CATCTATTTGTTCCT	54778
rs765622499	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:58995342	CAGAATTGTGTGTTT[A/C]CTGTTTTATTCAGTG	54778
rs765718834	snp	A/G	1.65839e-05	0.00287953	missense	RNF111	GRCh38.p7	15:59031648	ACTGAAGGAGAAGAA[A/G]ATTTGTTTGTTTCTG	54778
rs765720532	snp	A/G	1.64732e-05	0.0028699	missense	RNF111	GRCh38.p7	15:59066889	AACCACCATGCATTA[A/G]GACATCCTCATACAA	54778
rs765746456	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59027265	AGAACATAACTCTGA[C/T]ATGGGTTTCTGGAAG	54778
rs765751844	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59087079	GGTCTTGGATGTACT[A/G]AATCTCTATGAAAGT	54778
rs765756764	snp	C/T			downstream-variant-500B	RNF111	GRCh38.p7	15:59097561	ACTTCAGCATTTGAA[C/T]CATAACAGTTGACTT	54778
rs765767231	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59036136	GCTGGAGTGCAGTGG[C/T]GTGATCTTGGCTCAC	54778
rs765832194	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59016273	CTCCTGGATTCAAGC[A/G]ATTCTCCTGCCTCAG	54778
rs765871578	snp	A/G	1.64789e-05	0.0028704	synonymous-codon	RNF111	GRCh38.p7	15:59081183	ACACCAGCCAATTTC[A/G]CACCATATTCCAGCC	54778
rs765877108	snp	C/T	1.64817e-05	0.00287064	missense	RNF111	GRCh38.p7	15:59031091	AAGAAAAAAGTCTCG[C/T]TGTGAGGAAAAAACG	54778
rs765927431	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:58998924	TGTTACAAAGTCATG[A/T]CTGGGTGAAAGATCT	54778
rs765945736	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59048825	AGGTGCAGTGGCTCA[C/T]ACTTGTAACCCCAGC	54778
rs765958880	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59050420	GATGGTGGTTTCTGG[C/T]GAAAGGCCAGATTAA	54778
rs765959043	snp	A/G	4.95503e-05	0.00497722	synonymous-codon	RNF111	GRCh38.p7	15:59066798	ATCTAGTGCTGTAAC[A/G]GAAACTGGCCCTCCT	54778
rs765960985	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59047796	GCCCAGGCTGGATTG[A/T]ACTCCTTAGCTCGAG	54778
rs765991510	in-del	-/TT			intron-variant	RNF111	GRCh38.p7	15:58991936	AGGAGTTATTGTAAC[-/TT]TGTTAGGGATGATAA	54778
rs766054470	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59089602	GTCTTGAATTATTCA[A/G]TGTTAACAGTAAATC	54778
rs766065838	snp	C/G/T	3.30007e-05	0.00406195	missense, stop-gained	RNF111	GRCh38.p7	15:59085747	TATCACGCACCTCCT[C/G/T]GACTTCATCACTTAC	54778
rs766068230	snp	A/G	1.71776e-05	0.00293061	missense	RNF111	GRCh38.p7	15:59081283	ATGATGCAGCATCCA[A/G]CGTATGTTTTACGTT	54778
rs766111941	snp	A/G	6.88907e-05	0.00586861	intron-variant	RNF111	GRCh38.p7	15:59075912	AACATGAAATATTTG[A/G]CCAAACTTTAGAAAG	54778
rs766115179	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59007924	CAAACACATGTATAT[A/G]TAATTTTATCTGTCT	54778
rs766196560	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59062309	CAGCTTTCCAAAGTG[C/T]TGGGATTACAAGTGT	54778
rs766201608	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:58992916	CACACCTGTAGTAAT[A/C]CTAGCACTTTGGGAG	54778
rs766222162	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58990522	GAGCTTAGTGGTGTG[C/T]GCCTGTAGTCCCAGC	54778
rs766230673	snp	A/G	1.64863e-05	0.00287104	missense	RNF111	GRCh38.p7	15:59075981	GTGGACCTGAGCAAC[A/G]GTGGTATCAGAAGTC	54778
rs766308553	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59028504	TGATAAAACTTATGT[C/G]AATGTGGTCTCTCTC	54778
rs766363635	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59037804	TCACGCCATTGCACT[C/G]CAGCCTGGGCAACAA	54778
rs766366289	in-del	-/AAG	5.02668e-05	0.00501307	cds-indel	RNF111	GRCh38.p7	15:59066771	GTTTCAAGATGACTC[-/AAG]GAGAACTACATCTAG	54778
rs766383859	snp	C/T	3.63491e-05	0.00426301	utr-variant-5-prime, synonymous-codon	RNF111	GRCh38.p7	15:59030822	TTCCTTAAAGTTTCC[C/T]ATGTCTCAATGGACT	54778
rs766444315	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59070939	ACATCAGATCTTTAT[A/G]ATCTTTCATCACATT	54778
rs766445832	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59073102	TGCTTGAGCTGGGTA[A/G]GTGGAGGCTGCAGTG	54778
rs766483893	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59091569	CATCATATGGCAGTA[C/G]TGTAATTTTTTTAAC	54778
rs766512672	in-del	-/TCTCT			intron-variant	RNF111	GRCh38.p7	15:59001336	TAGCCATTTTTTACC[-/TCTCT]TCTCTTTTCTGGATT	54778
rs766516735	snp	C/G	3.29766e-05	0.00406045	synonymous-codon	RNF111	GRCh38.p7	15:59076178	GCCCCCTCCACAGCC[C/G]TCTCTCTCATCATGT	54778
rs766546595	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58994581	CTCCCAGGTTCAAGC[A/G]ATTCTCCTACCTCAG	54778
rs766559103	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59085820	AAATTTTGACATGTT[C/G]TAAAAGTTCCTTTTC	54778
rs766598880	in-del	-/CAGCC			intron-variant	RNF111	GRCh38.p7	15:59003070	TATTAAAGCTTACTG[-/CAGCC]CAGCCTTGAACTCCT	54778
rs766606625	snp	C/T	3.33439e-05	0.00408299	intron-variant	RNF111	GRCh38.p7	15:59076253	CAAAATCTAGAGTCA[C/T]GTCAATGAAGCATTT	54778
rs766608280	snp	A/G	1.64882e-05	0.00287121	missense	RNF111	GRCh38.p7	15:59031361	GAAGCCATAGTGCAC[A/G]GTCTCATAAGTGGCC	54778
rs766614000	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59057270	TTAGTATTGCCAAGG[C/T]TGAGAAACCCTGGTT	54778
rs766614165	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59045619	GTAATGCCCAGTTTA[C/T]GGGTTGAAATAAGGA	54778
rs766639850	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59005267	CCTGGGCACAAGCAG[A/T]CCTCCCTGCATGAAG	54778
rs766649439	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59074088	GTAGTGGGTCTCAAC[A/G]GTATTCTTAAAATAT	54778
rs766679654	in-del	-/C			intron-variant	RNF111	GRCh38.p7	15:59060002	CAGGAAGTATTCTCT[-/C]CCCCTGGAAAACTGA	54778
rs766687577	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59004531	GTTTGTTAAATAAAG[C/T]AGCTGACATCAGTAT	54778
rs766691282	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59071463	TGAGACGGGTGGATC[C/G]CTTGACCGCAAGAGT	54778
rs766694524	snp	G/T	1.64732e-05	0.0028699	missense	RNF111	GRCh38.p7	15:59058493	AGCCAACCTTCCACA[G/T]TGTCAGAGACTTCAG	54778
rs766694941	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59044091	GCTGGAGTGCAGTGG[C/T]GCAATCTCGGCTCAC	54778
rs766712884	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59044887	ATGCCAAAATGTTGC[C/G]TGTTGTGAATATGCT	54778
rs766714928	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59032735	GTTATCATGTTCTTT[A/G]TAGCTGAAAAGTAAT	54778
rs766762540	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59016052	GACAGGGTTTTGCCA[A/T]GTTTTGACCTCCTAG	54778
rs766772911	snp	C/G	1.71255e-05	0.00292617	intron-variant	RNF111	GRCh38.p7	15:59031732	GCTGAGTAAAACATG[C/G]AACCTATTGCATTGC	54778
rs766785730	snp	C/G	1.64784e-05	0.00287035	missense	RNF111	GRCh38.p7	15:59052347	TAGAAGCTTCCTCCA[C/G]TCCCCAGGTTACTGC	54778
rs766792484	in-del	-/TTTTT			intron-variant	RNF111	GRCh38.p7	15:59000164	GATTTTTTTTTTCCC[-/TTTTT]TTTTTTTTTTTTTGA	54778
rs766802133	snp	C/G	6.64121e-05	0.00576209	intron-variant	RNF111	GRCh38.p7	15:59091033	TCATCTTGGCTTTTA[C/G]CAGTCATTATATTCT	54778
rs766809048	snp	A/G			utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096700	TAGAAGGTCAGGGGA[A/G]AGTGAAGGAGTCAGT	54778
rs766809110	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59042759	GGGCCTGTTTATGGA[C/G]TTTTTACTCCGTCTT	54778
rs766822871	snp	C/G	0.00061106	0.0174687	synonymous-codon	RNF111	GRCh38.p7	15:59089684	TCCTGATATGGCAGG[C/G]TATCCTCACATCCGT	54778
rs766856949	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59094399	TTTGAGATAATATGT[A/G]TTTTTAAAGGGCATT	54778
rs766890214	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59037260	AAGTGATATGTTACT[G/T]GGGTTATTAGAAAGC	54778
rs766899234	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59046452	CCCACCTCAGCCTAC[A/C]AGATTGCTGTGATTA	54778
rs766906725	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59067194	TGTCTCTCTCCCTCC[C/G]TCCATTTCTCTCCCT	54778
rs766923187	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59056172	AAGTAGAAGCAGTAC[G/T]TTTTAAATATAAACA	54778
rs766948559	snp	A/G	1.64814e-05	0.00287061	missense	RNF111	GRCh38.p7	15:59031339	ACCATTTTGAATGCT[A/G]AAAGTAGAAGCCATA	54778
rs766983334	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59087295	TGATAATACTATGCT[C/T]TGAACAAAGGATTCT	54778
rs767013306	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59060562	ATCATGTGATCCTGA[C/T]AAGTTGAGGCTACAG	54778
rs767039360	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58989757	GAGAAAAGCACCTTG[C/T]TTGTATAAAGCTAAG	54778
rs767041334	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59000746	TGCTGCTGCAGAGAA[A/T]TAACCAATTTTTGAT	54778
rs767073260	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59088583	TAATGTCAGAGATTT[A/T]TTTATAAAGATGGAA	54778
rs767073731	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59032262	TACATTTTATACATA[C/T]TAGATTATATTTTAT	54778
rs767076649	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59008246	TTTGGAGACAAGAGT[C/T]TTTCTCTGTTGCCCA	54778
rs767089674	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59070059	TTTTTTTTTTTTTTT[-/A]AGAGAGGATCTTGCC	54778
rs767091118	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59059688	AGCTCTTATCTCAAG[C/G]TAGTTCTTACGTTTC	54778
rs767093264	snp	A/G	1.73921e-05	0.00294885	intron-variant	RNF111	GRCh38.p7	15:59031746	GGAACCTATTGCATT[A/G]CATTTGTGCTTAATT	54778
rs767171858	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59007516	CTATTATGAGTAAAG[C/T]GATGAACATTCATAT	54778
rs767172872	snp	G/T	1.64743e-05	0.00287	missense	RNF111	GRCh38.p7	15:59076083	ATCTTTGGCCATCAG[G/T]CCGCTGCTGCTGCCC	54778
rs767194111	in-del	-/TTTG			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986207	TGTGTGTGTGTGTGT[-/TTTG]TTTGTTTGTTTGTTT	54778
rs767198954	snp	C/G/T	0.000149962	0.00865796	intron-variant	RNF111	GRCh38.p7	15:59058595	TTTTGTCATTACTTT[C/G/T]GTTAGGAAAAGTATT	54778
rs767204442	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58991875	AGAAAGTCATTTTTG[A/G]AACATTGGGGGAAAT	54778
rs767206571	snp	C/T	3.46921e-05	0.00416471	synonymous-codon, intron-variant	RNF111	GRCh38.p7	15:59084102	TTCAATTATTTCCAG[C/T]GGTCTTTTTGTGTTC	54778
rs767236764	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59002048	AATGAGGTTAATGAC[A/G]TGGGCACTGTGTAGG	54778
rs767243279	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58992467	GTGATGGGTACATGG[A/G]TATTAATAATATTGT	54778
rs767249622	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59053754	CCTATTTTTCCTTGT[A/G]GGACTAGAGATCTTG	54778
rs767274349	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59070883	TCTCCAGCCCCTCAG[C/T]TTCCAGTATTGCACA	54778
rs767278991	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59012341	CTGTCTTAATTTCCA[C/T]TTAGGTAATTACAGT	54778
rs767294754	snp	C/T	3.295e-05	0.00405881	missense	RNF111	GRCh38.p7	15:59067031	AAAGACCTCCACAAG[C/T]ACAAGCACCTTGTGG	54778
rs767299553	snp	A/T	1.65061e-05	0.00287277	intron-variant	RNF111	GRCh38.p7	15:59094759	AAAATTAATTTTTGC[A/T]TTTTGTTTTCTTGCC	54778
rs767324843	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59002818	TTTGCACCTGTTAGG[C/T]ATATTCCTGTCACAT	54778
rs767328137	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59022792	GCATAGACACATCCA[A/G]TAAGGAGATTGCCTG	54778
rs767333720	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59017290	AGAGATCGTAAATGC[A/G]TCATTCAGCATATGT	54778
rs767339680	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59056589	CAGGTAGATGGAAAG[A/C]GTTGATAGGTGGAAA	54778
rs767341181	snp	C/T	1.78178e-05	0.00298473	intron-variant	RNF111	GRCh38.p7	15:59055863	AAATTGAAGTAGTAA[C/T]AGTAGAAAATTATGA	54778
rs767359117	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59038894	TATAAAGTTCCCCTT[C/G]ACTGTTTTCTGTAAT	54778
rs767416400	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59011522	ACAAAACTTTACTTA[A/C]TCCTAGTTCTGTAGA	54778
rs767430879	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59064628	GGGGCAGTTAGAGGT[C/T]AGTGTCAGTTTGTAT	54778
rs767431118	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59051191	TGGTGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	54778
rs767431138	snp	C/T	1.64751e-05	0.00287007	missense	RNF111	GRCh38.p7	15:59031246	TGTCTTTCTTCTCCT[C/T]CATCTAGTCTGCATT	54778
rs767447416	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59053078	TCAATATGTTACTCA[C/T]TGATACCAGTGAAAC	54778
rs767457369	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59065470	TCTTTTCTAACAACC[A/T]TGCAAGGCAATTTTA	54778
rs767462658	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59010401	TTTATTTATTTATTT[A/T]TTTTTTCTTTCTTTT	54778
rs767470409	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59069848	TGAGATTTGTGATTT[A/T]GTAGATATCTTATGT	54778
rs767520088	snp	C/T	1.64735e-05	0.00286993	utr-variant-3-prime	RNF111	GRCh38.p7	15:59094917	ACCATGTTTCAGAAC[C/T]CTTGCCCTCCCTCTC	54778
rs767528373	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59092911	AGACTAAGGCAGGAG[A/G]ATGGCTCAAGCCCAG	54778
rs767543809	in-del	-/TATC			intron-variant	RNF111	GRCh38.p7	15:59080628	ATATACACAGATATT[-/TATC]ATAGCATTTGGGTTT	54778
rs767571140	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59004377	TGTGTAGATGAGACT[G/T]AACGTGTACAAGAAT	54778
rs767581446	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59031737	GTAAAACATGGAACC[G/T]ATTGCATTGCATTTG	54778
rs767587259	snp	C/G	3.29891e-05	0.00406122	synonymous-codon	RNF111	GRCh38.p7	15:59081000	TTCTCATGGAAACCC[C/G]CCTCCTCAGACTCAG	54778
rs767596938	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59081400	TTGTAGTCACAGCTC[C/T]TTGGGAGGCTGAGAC	54778
rs767622595	in-del	-/TT			intron-variant	RNF111	GRCh38.p7	15:59049364	CCAGGTGTCTTTGAT[-/TT]TTTTTTTTTTTTTTT	54778
rs767635363	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59072796	TACCTGGAGAAGATT[C/G]TATCTCAAGAAACCA	54778
rs767654428	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59043692	TTCATTTCTGTTGGA[A/G]AGATACCAACAGAGG	54778
rs767750345	snp	G/T	4.95495e-05	0.00497718	synonymous-codon	RNF111	GRCh38.p7	15:59031446	TGGCAGTTCGTTACG[G/T]AGACTTCCATGCAGA	54778
rs767757508	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58999670	TAATACATTTTAAAG[C/T]ATTTATGAGTTTTAC	54778
rs767767290	snp	C/T			utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096419	TTAATAAATAACTTA[C/T]ATTTCTATTGTCTTT	54778
rs767778166	snp	A/G/T			utr-variant-3-prime	RNF111	GRCh38.p7	15:59095044	TGGTACAACTAATGC[A/G/T]AGACCTACAGTTTAT	54778
rs767795066	in-del	-/ATT			intron-variant	RNF111	GRCh38.p7	15:59060786	GTAGCTTTATGTAGC[-/ATT]ATTATTATTATTATT	54778
rs767800684	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59013903	AAGTAATTCTTATGC[C/T]TCAGCGTCCCGAGTA	54778
rs767802569	in-del	-/TCTTTTTTT			intron-variant	RNF111	GRCh38.p7	15:59017752	CATTATTTGTTGAAC[-/TCTTTTTTT]TTTTTTTTTTTTTTG	54778
rs767811051	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59025428	TGAAATTTTGGCTAT[G/T]TAGAATATGTAACAA	54778
rs767812358	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59084695	GTCACCATGCTGTGC[A/C]GTAGAATATCAGAAC	54778
rs767813521	in-del	-/CTCCC			intron-variant	RNF111	GRCh38.p7	15:59067257	TTTTTTTTTTTTTAA[-/CTCCC]TCCCATTCTTCCTTC	54778
rs767826744	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59014697	AAGAAAGCATGTTAT[C/G]AGGAAAACTGCCATG	54778
rs767836408	snp	C/G/T	4.96539e-05	0.00498246	intron-variant	RNF111	GRCh38.p7	15:59091045	TTACCAGTCATTATA[C/G/T]TCTTCACTTTCAGGA	54778
rs767836960	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59085559	GCTTTGTAAGTTAAG[A/G]AACCTTAGATTACTT	54778
rs767841131	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59055930	GAAACTCCTCCTGCT[A/T]ACTGGTAATATATTA	54778
rs767842846	snp	A/C/G	4.94909e-05	0.00497428	missense	RNF111	GRCh38.p7	15:59031538	TGCAGAGGAAGAAAC[A/C/G]AGAAGTGTTAGCTCG	54778
rs767845694	in-del	-/AGTG			intron-variant	RNF111	GRCh38.p7	15:59003170	CGCAGGCTGGAGTGC[-/AGTG]AGTGGCTCAATGTCA	54778
rs767884130	snp	A/C/G	3.29594e-05	0.00405941	missense, synonymous-codon	RNF111	GRCh38.p7	15:59052369	GGTTACTGCCAATGA[A/C/G]GAAATTAATGTTACC	54778
rs767897839	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59026113	AAAGTTGAAACAAGT[A/G]TTCATATTTATAATT	54778
rs767907077	snp	C/T			intron-variant, utr-variant-5-prime	RNF111	GRCh38.p7	15:58988268	GGGCAAGGCATTCGT[C/T]TACCGACACACCCAC	54778
rs767915296	snp	A/G	5.01987e-05	0.00500967	intron-variant	RNF111	GRCh38.p7	15:59076260	TAGAGTCATGTCAAT[A/G]AAGCATTTTGTACTT	54778
rs767926231	snp	A/G	1.67399e-05	0.00289304	intron-variant	RNF111	GRCh38.p7	15:59091186	TGAAACTTCTGGAGT[A/G]TTACTGAAAGGCATA	54778
rs767987776	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59034719	TTTTGAGTGATTCAA[A/G]TAAAATGATTTGGCA	54778
rs768002917	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59076961	TTACATATCTTCTTG[A/G]ATTTTTTCTTCTACT	54778
rs768039046	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59054589	CCACAACTGTTTCTG[A/G]TATGTACTATCCTAT	54778
rs768045520	in-del	-/C			intron-variant	RNF111	GRCh38.p7	15:59072894	TTAAAAAAAAAAAAA[-/C]AAAACACTTCCAGCT	54778
rs768079417	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59035536	GCAAATTTCTGAGCT[C/G]GTTTGAATTTCTCCC	54778
rs768126587	in-del	-/G			intron-variant	RNF111	GRCh38.p7	15:59075860	TAATTTAAAGATTAT[-/G]GTTTTTTTGGTTATA	54778
rs768141934	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59037346	TGTTTTGTTACTGCA[A/G]TATGTCAAGAACTCC	54778
rs768175008	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59053039	TGATGTTGAAATAGC[C/T]CTTTCTGTTAGAATC	54778
rs768213317	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58991785	CAGATGATGTAGACA[A/G]ATTAAAATTATTTTA	54778
rs768234342	in-del	-/C			intron-variant	RNF111	GRCh38.p7	15:58996080	TAAAGCAATTTTTTT[-/C]TTCTTTTCTTTTTCA	54778
rs768254472	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59070682	CAAAAGAAAGGAGCT[C/T]CTCCTTTTCTCTTTC	54778
rs768275029	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59023090	TGTCTCTACTAAAAA[C/T]ACAAAAAATTAACTG	54778
rs768279175	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59034270	GCAACATTGTGCTTG[C/T]GTTTTATACACCTAT	54778
rs768304653	in-del	-/C			intron-variant	RNF111	GRCh38.p7	15:59049900	GTGCGTGCCACCACA[-/C]CCGGCTAATTTTTGT	54778
rs768313009	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59029009	GATCTCGAACTCCTG[G/T]CCTCCAGTGATCCGC	54778
rs768323419	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59082933	AAATTGTTGTTTAGA[A/G]TAAACATGCAAAATC	54778
rs768324073	in-del	-/A	1.6596e-05	0.00288058	intron-variant	RNF111	GRCh38.p7	15:59091035	ATCTTGGCTTTTACC[-/A]GTCATTATATTCTTC	54778
rs768349415	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59012219	AGACACAGTTTCACT[A/G]TGTTGGCCAGGCTGG	54778
rs768367611	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59086766	AATTTTAGGAGTGAG[A/G]GTCAGGCAGCAGTGA	54778
rs768369324	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59023378	GTTATAATTGTTTTC[A/T]TGTAGGTCCTTTGTG	54778
rs768382770	snp	G/T			upstream-variant-2KB	RNF111	GRCh38.p7	15:58987540	AGTACAAAGGGGGAG[G/T]GCCGGGACCGAGGGG	54778
rs768399663	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59002289	CACTTGAAATTTTAC[A/T]TTTAAAGATCAACTC	54778
rs768404353	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59076326	TTTTAGTATTTACTT[A/G]GCTTAAGAGTAGGGT	54778
rs768404441	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59064106	AGCATAGCCCTAAAA[C/G]ACTTTTGATCATGGT	54778
rs768404496	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59081390	TGGCATGCACTTGTA[A/G]TCACAGCTCCTTGGG	54778
rs768429982	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59022714	AATGTCTTTTAAATG[C/T]AACCAAAAGACTCAC	54778
rs768444286	snp	C/G	3.36038e-05	0.00409888	synonymous-codon	RNF111	GRCh38.p7	15:59030861	TAACGAGCTCTACAC[C/G]TTAAAAGTGGATATG	54778
rs768446057	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59082037	CTCCCATGATCATGC[C/T]ACTGCACTGCAGCCT	54778
rs768462078	in-del	-/AGTT			intron-variant	RNF111	GRCh38.p7	15:59056812	AATTAATGATTACTC[-/AGTT]AATTAAATATAGGGT	54778
rs768473439	snp	C/G	1.65455e-05	0.00287619	intron-variant	RNF111	GRCh38.p7	15:59058567	TATGTAAAAAAGTGG[C/G]GGAGGGGAGACTTTT	54778
rs768487155	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59003410	CACCCGGCCTTTTTC[-/T]TTTTTTGAGACAGAG	54778
rs768529027	snp	C/T	1.66477e-05	0.00288506	intron-variant	RNF111	GRCh38.p7	15:59076245	AGTGGACACAAAATC[C/T]AGAGTCATGTCAATG	54778
rs768533219	snp	A/C	1.87345e-05	0.00306054	missense	RNF111	GRCh38.p7	15:59092547	CACAGAGGAAACTGC[A/C]CTGCAAACAAGATGG	54778
rs768582160	snp	A/G			upstream-variant-2KB	RNF111	GRCh38.p7	15:58985734	TTATTTCAACATATA[A/G]TAAATATTAAAAAGT	54778
rs768582575	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58998093	TATTTTTAGTAGAGA[C/T]GTGGTTTCACTATGT	54778
rs768619194	snp	C/T	1.66305e-05	0.00288357	synonymous-codon	RNF111	GRCh38.p7	15:59080976	TCATCAAGCTTCTGC[C/T]TGCCCGCATTCTCAT	54778
rs768681699	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59006169	TGTATTCCAGATTTT[A/G]TATAGTGAACTTATT	54778
rs768684597	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59044680	GTCTTAGCCATACTC[A/G]TTTTTTATCCTTTAG	54778
rs768695057	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58989239	CACCCTAGTCTGGTT[A/G]TATTTGTGAGGTGAA	54778
rs768695991	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59033332	TCTTTTTGCCAGAAC[A/C]CTAAACCAGTAACCT	54778
rs768738102	snp	C/T			utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096200	GGAAGTTTTAATCTA[C/T]TTCAGGATGCATATT	54778
rs768755359	snp	C/G/T	1.67789e-05	0.00289641	synonymous-codon	RNF111	GRCh38.p7	15:59031698	CAATCCAGCTGTTCC[C/G/T]TCAGGTAAAAATGTT	54778
rs768761060	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59052569	TATCAGATTAGTGGA[-/T]TTTTTTTTTTTTTTT	54778
rs768770705	snp	C/T	3.29457e-05	0.00405854	synonymous-codon	RNF111	GRCh38.p7	15:59066879	GTCGTCACAGAACCA[C/T]CATGCATTAGGACAT	54778
rs768780563	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59047481	GCCTGGGCATTGGAT[C/G]AAGACACTTTCTCAA	54778
rs768802087	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59026934	CTTGCTCTCCTCTAC[C/G]CTTGTCTCATTGGAC	54778
rs768819504	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59068019	AGTATTGGCAATCAC[A/G]TGGAGTAAAAGAAGT	54778
rs768836549	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59048357	AAAAGTGTATGCAAT[A/G]TGTGACTCCACTTAA	54778
rs768843625	in-del	-/G			intron-variant	RNF111	GRCh38.p7	15:59085877	TATATTAATATAGAT[-/G]TTTTAATAGAATTTG	54778
rs768858668	snp	A/C	1.64741e-05	0.00286998	missense	RNF111	GRCh38.p7	15:59066986	CTGTCCCAGTTTCTC[A/C]TTCCTTTAGTGATCC	54778
rs768922375	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59036762	TAATATCTTAAAATA[C/G]TCCAAGACCCAACAG	54778
rs768923322	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59057807	AAGTATGTGATCTCA[A/G]TTCATCCTAATGACA	54778
rs769011436	snp	C/T			missense	RNF111	GRCh38.p7	15:59066842	TACCTTCCTGCTGTC[C/T]CCAGCACTCACCATG	54778
rs769030367	snp	A/G			missense	RNF111	GRCh38.p7	15:59031379	CTCATAAGTGGCCTC[A/G]GACTGAGACAGAATC	54778
rs769063525	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58995521	TGGAGTGCAGTGGCG[C/T]GATCTTGGCTCACTG	54778
rs769071484	snp	A/G	0.000141193	0.00840099	intron-variant	RNF111	GRCh38.p7	15:59093514	CTGCACTCGGCTATA[A/G]CATCTTTTATAAACT	54778
rs769112956	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59089419	TCTTAAGACAATTTT[A/G]CTCTTTTCAAGTTTG	54778
rs769160814	snp	A/C/T	4.97742e-05	0.00498849	missense	RNF111	GRCh38.p7	15:59055788	AGGATTTCTACTGTT[A/C/T]TACAGCCCTTGAGGC	54778
rs769197910	in-del	-/CTGT			intron-variant	RNF111	GRCh38.p7	15:59044024	CTCACAGATTGGAAA[-/CTGT]CTTTTTTTTTCTGGT	54778
rs769223221	snp	A/G	1.64751e-05	0.00287007	missense	RNF111	GRCh38.p7	15:59094818	TTTTCCACCAAGTGT[A/G]TGTTGACCAATGGTT	54778
rs769225789	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59047867	GGCGTGAGCCACTGT[-/A]TCCAGCCTACTTATT	54778
rs769252681	snp	A/G	1.64751e-05	0.00287007	synonymous-codon	RNF111	GRCh38.p7	15:59031161	TGTTAAAGAAAACCA[A/G]GGAATATTAGGACTG	54778
rs769288211	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59023141	TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	54778
rs769332464	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59018082	GAGCTCTTATAGACT[A/C]CTTTCCATTAATGCA	54778
rs769334534	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59030670	TAATTCATAACAGAC[A/G]TTTTGTGTACTGATG	54778
rs769340593	snp	C/G/T	3.29556e-05	0.00405918	missense	RNF111	GRCh38.p7	15:59031307	AGGATAAAGAAGTCT[C/G/T]TGTAAGACATTCCCA	54778
rs769341708	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59011127	TTCATCATTAATTAT[A/G]TAGTTTATTCAGGGA	54778
rs769375295	snp	A/G	1.66529e-05	0.00288551	missense	RNF111	GRCh38.p7	15:59031679	CCAGTGAAAACCACC[A/G]AAACAATCCAGCTGT	54778
rs769383574	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59052842	TCTTTTTAAAAGCAC[C/T]CCAAGTATACAATGA	54778
rs769393050	snp	C/T	1.64762e-05	0.00287016	synonymous-codon	RNF111	GRCh38.p7	15:59076055	CTGCCCTGTTTCTTC[C/T]TCCCGAGCTGCAATC	54778
rs769457033	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59064762	TTGGAAAAAACGAAT[-/A]TACAGAAATTTAGAT	54778
rs769476525	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59074805	TAGCTTTTGGCCTCT[C/T]TGGGCTTTTGACATG	54778
rs769505517	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59033320	TCTGTATTTTTCTCT[C/T]TTTGCCAGAACCCTA	54778
rs769516864	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59032628	GTTTTGCCAAGTTGC[C/T]CAGGTTGGTCTTGAA	54778
rs769518778	in-del	-/AATT			intron-variant	RNF111	GRCh38.p7	15:59013594	AGCACTGATTTGATC[-/AATT]GTGATCAGCTGGCTG	54778
rs769529537	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59091889	ATGCACAGTTTACAA[C/T]AGGGTTCACGCTTCT	54778
rs769554330	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59039451	TTGTTCTAGCAGCAT[C/T]CAAAGAGGTTTTTTC	54778
rs769592883	snp	A/T	1.64735e-05	0.00286993	missense	RNF111	GRCh38.p7	15:59081118	GCACCCCCACCACCA[A/T]CTCACTTAGCCAGTA	54778
rs769622755	snp	C/T	0.000115396	0.00759505	missense	RNF111	GRCh38.p7	15:59089668	TTCTGTTGAAATAGG[C/T]TCCTGATATGGCAGG	54778
rs769668634	in-del	-/TTTTTTT			intron-variant	RNF111	GRCh38.p7	15:59019106	TTTGTATTTTTGTAT[-/TTTTTTT]TTTTTTTTTTTTTTT	54778
rs769674265	snp	A/G	4.97137e-05	0.00498542	intron-variant	RNF111	GRCh38.p7	15:59058576	AAGTGGGGGAGGGGA[A/G]ACTTTTTGTCATTAC	54778
rs769708663	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59035395	AGTCCAAAGTCTCAT[C/G]TGAGACAAGGCAAGT	54778
rs769718553	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59004185	TTAAGGTCTCAACTT[C/T]GTTTTTAGTTATCTT	54778
rs769719630	snp	C/T			utr-variant-3-prime	RNF111	GRCh38.p7	15:59097103	ACTGCCATTAGTTAT[C/T]GAAAAATGTGATAAG	54778
rs769728745	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58995016	ATAGGACCCAGTTCA[A/G]GATCACAAAATGCAT	54778
rs769753405	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59056696	TACCCAGTTGTTTAT[A/G]AAGAGATAACAACTG	54778
rs769797375	snp	A/C	1.64735e-05	0.00286993	missense	RNF111	GRCh38.p7	15:59067000	CCTTCCTTTAGTGAT[A/C]CTGCTTGCCCTGTGG	54778
rs769853453	snp	A/G	1.65015e-05	0.00287237	missense	RNF111	GRCh38.p7	15:59031591	AGTTCTAGTAGTTCC[A/G]GTGAGAATGACCTCA	54778
rs769862737	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58989724	AGATTATTGAGAGAG[A/G]GCTGTTGTGATGTTT	54778
rs769872621	snp	A/G	1.88124e-05	0.00306689	utr-variant-5-prime, synonymous-codon	RNF111	GRCh38.p7	15:59030804	AATTTTGTCTTCTAG[A/G]CTTTCCTTAAAGTTT	54778
rs769889903	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59004309	AGGAACTTGCTGTTT[A/T]GGTTTACTGAAACTA	54778
rs769929043	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59047656	TCTTGGCTCACTGCA[A/G]CGTGCGTCTCCCAGG	54778
rs769943760	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59036646	TACAATTCAAGGTGA[C/G]ATTTGGGTGGGGACA	54778
rs769978896	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59060293	TTATATGTTATTGTA[C/T]ATATTTTAATTCTTA	54778
rs769985525	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59017194	TTCTACGAATCCGTT[C/T]CCTGGTGCCAAAAAG	54778
rs770001582	snp	G/T	1.67005e-05	0.00288963	intron-variant	RNF111	GRCh38.p7	15:59052434	GAGAAAGCTATCGGT[G/T]AGATTTTAATTCTTA	54778
rs770006201	snp	C/T	1.64735e-05	0.00286993	missense	RNF111	GRCh38.p7	15:59094884	ACATTGAGGCCCAGC[C/T]GCCAAGTGAAAGTTG	54778
rs770022813	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59025084	CAGTGGACACTTGAG[A/G]TGCTTCCACCTTTTG	54778
rs770042079	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59007244	GTCCTTTCCCCATCC[C/G]TTGAAGACACAACCA	54778
rs770072723	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59087965	CTTAGATTACGTACG[C/G]TAAGGAAGTGAAAAC	54778
rs770090491	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59036182	CTGGGTTAAAGTGCC[C/T]GAGTAGCTGGGATGA	54778
rs770094402	snp	A/G	1.65192e-05	0.00287391	synonymous-codon	RNF111	GRCh38.p7	15:59081264	GGAAGTTCAAAGGAG[A/G]AGGATGATGCAGCAT	54778
rs770100063	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59059530	CCAAAATAATTGAGA[A/G]TGGGGATGGGAGTTT	54778
rs770156665	snp	A/T	1.65655e-05	0.00287793	missense	RNF111	GRCh38.p7	15:59091145	TACATATCCACATAA[A/T]TACAAAAAGGTAAGA	54778
rs770157640	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59002538	TGAGTGAAAGCCCTC[A/G]TAACTGTGCATTTAA	54778
rs770160861	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59089272	AATCAAGCAAAAAAG[G/T]CATAGGGTACTTTGG	54778
rs770206917	in-del	-/GTTTTG			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986206	TGTGTGTGTGTGTGT[-/GTTTTG]TTTGTTTGTTTGTTT	54778
rs770222233	snp	A/G	1.64746e-05	0.00287002	synonymous-codon	RNF111	GRCh38.p7	15:59031194	GCAACACCTAGGGAC[A/G]CCAAGTGATGAAGAT	54778
rs770225597	in-del	-/GT	1.64773e-05	0.00287026	frameshift-variant	RNF111	GRCh38.p7	15:59031303	GATGAGGATAAAGAA[-/GT]CTCTGTAAGACATTC	54778
rs770256214	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:58992544	TTTTTTTGGCTGGGC[C/G]CAGTGGCTCATGCCT	54778
rs770259949	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59028163	TGAATCCTCCGATGA[C/T]CCCCAGCCCTAGGTA	54778
rs770308265	snp	C/G	1.64803e-05	0.00287052	synonymous-codon	RNF111	GRCh38.p7	15:59031320	CTCTGTAAGACATTC[C/G]CAGACCATTTTGAAT	54778
rs770319973	snp	A/C	2.29108e-05	0.00338451	intron-variant	RNF111	GRCh38.p7	15:59084081	AAGAAAAGAAATAAC[A/C]AATTATTCAATTATT	54778
rs770349982	in-del	-/CGCCT			intron-variant	RNF111	GRCh38.p7	15:59022984	GGGCGCGGTGGCTTA[-/CGCCT]GTAATCCCAGCACTT	54778
rs770368125	snp	A/T			intron-variant, missense, utr-variant-5-prime	RNF111	GRCh38.p7	15:59022519	ATAGCATGAGCAGTA[A/T]TATCCAGACCAACAT	54778
rs770390047	snp	G/T	1.64825e-05	0.00287071	missense	RNF111	GRCh38.p7	15:59076142	CTATGGATCAAGCAT[G/T]GTTGCGCAGCCCCAG	54778
rs770391875	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59080718	GTTGTGAAGCTGTGA[A/G]TGAAGTTAAACTATA	54778
rs770396007	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59053522	TAGAACATGCTTTTC[C/T]ACTTGCCATTTTAGC	54778
rs770446253	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58994955	ATTTTCCAGTTTTGT[C/T]GAATTGTCCTGATAA	54778
rs770458829	in-del	-/AA			intron-variant	RNF111	GRCh38.p7	15:59017625	ACAGGAAGTTAAAAT[-/AA]CAGAAATCTCTAAGA	54778
rs770477997	snp	A/C	1.65712e-05	0.00287843	intron-variant	RNF111	GRCh38.p7	15:59058338	TGAAATGCTAAGTTG[A/C]CATTTTGTATTTTGT	54778
rs770479491	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59040938	AGAGTCAAAACTTTA[A/C]AACAAGATATACTCA	54778
rs770491922	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59058075	TTGTGATAGATCAGA[C/T]AACTTATTTAGAAGC	54778
rs770497599	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59009839	CTCATGTCTCTAGTC[C/G]CAGTTACCTGGGAGG	54778
rs770538437	in-del	-/TCCC			intron-variant	RNF111	GRCh38.p7	15:59067258	TTTTTTTTTTTTAAC[-/TCCC]TCCCATTCTTCCTTC	54778
rs770543575	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59043324	CTCAGCCAGCTGATT[G/T]TTTTATTATTTGGTA	54778
rs770570053	snp	C/T	1.64735e-05	0.00286993	synonymous-codon	RNF111	GRCh38.p7	15:59058441	AAATCCATCTACCTC[C/T]GAGCAGGCCTCTGAT	54778
rs770575371	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59004946	AGACCCAGTGGAGAG[C/T]AGCAAAATTTAATCT	54778
rs770578829	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59056610	TAGGTGGAAAGAGTT[A/G]GAGGCCATATACAAT	54778
rs770611002	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59018158	TGGTTTGATAAATTA[C/T]TATCATTTTCGAGCA	54778
rs770614096	snp	G/T	4.9445e-05	0.00497193	missense	RNF111	GRCh38.p7	15:59031332	TTCCCAGACCATTTT[G/T]AATGCTAAAAGTAGA	54778
rs770626474	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59073597	GTTCCAACTTCTTAT[G/T]CTAGTTCTCTTGCTG	54778
rs770631307	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59032510	CACTGCAACCTTCAC[C/T]TCCTGGGCTGAAGCC	54778
rs770695954	snp	A/C/G	3.29474e-05	0.00405867	synonymous-codon	RNF111	GRCh38.p7	15:59066867	ACCATGTGGAGGGTC[A/C/G]TCACAGAACCACCAT	54778
rs770720789	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59061872	TTTCATAATGAATAA[A/G]CATGATCTTTTAAAA	54778
rs770789298	snp	A/C	3.30142e-05	0.00406276	intron-variant	RNF111	GRCh38.p7	15:59089774	GGTATGTAATAAAAT[A/C]AATGAATATGTTTGT	54778
rs770865099	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59045936	TCTGCCTGTAAGATA[C/T]ATTTGCACTGTTAAA	54778
rs770865510	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58989124	CACAACTTCTGTAAC[A/G]CTGGACTTAGCTTTA	54778
rs770874215	snp	C/G	1.67052e-05	0.00289004	missense	RNF111	GRCh38.p7	15:59031690	CACCAAAACAATCCA[C/G]CTGTTCCCTCAGGTA	54778
rs770907486	in-del	-/AAAC			intron-variant	RNF111	GRCh38.p7	15:59048930	TCCTGTCTCTTTAAA[-/AAAC]AAACAAACAAACAAA	54778
rs770959037	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59075247	CAAACCTTCAATTTA[C/T]TAAAAATAAAACAAA	54778
rs770981816	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59052446	GGTGAGATTTTAATT[C/G]TTAGTTAAATGTTTG	54778
rs770983452	snp	C/G	0.000382162	0.0138179	synonymous-codon	RNF111	GRCh38.p7	15:59092563	CTGCAAACAAGATGG[C/G]GAAGAAGGGACTGAG	54778
rs770994336	snp	A/T	1.6654e-05	0.00288561	intron-variant	RNF111	GRCh38.p7	15:59091167	AAGGTAAGAATTTAT[A/T]CTATGAAACTTCTGG	54778
rs770995075	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59006318	TCAGGACATAAAACA[G/T]TCCATCACTCTAGAA	54778
rs771013506	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59007141	ATTTAAGTTTTGCCA[A/G]ATGCATCTATTTATT	54778
rs771024059	snp	C/G	1.64876e-05	0.00287116	missense	RNF111	GRCh38.p7	15:59030943	ATCCTTTTGCATCCA[C/G]AGCCCATTGGGGCAG	54778
rs771037890	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59026010	GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCC	54778
rs771039800	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59013477	TAGGTTAGTGGAATG[C/T]TTTTCTCATAGTTTG	54778
rs771049912	snp	G/T	2.26488e-05	0.0033651	intron-variant	RNF111	GRCh38.p7	15:59030780	ACATTAAAAATCTTT[G/T]AAATATCTAATTTTG	54778
rs771085524	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59086897	GTTAGATCACCTCCT[C/G]AGTTATGTGGAAAAA	54778
rs771088096	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59087774	TACATGTAAGCAGAC[A/C]CATGCAGTTCAAACC	54778
rs771147090	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59027169	TTATCAACATGAGGA[C/G]TTAGTAATTACGGAT	54778
rs771169916	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59058032	GTGCATAGTAAGGAA[C/T]TTTTATTTCCTTTTA	54778
rs771240112	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:58991464	CATTCTGTTCTGTGT[G/T]TGGGAACATAATAAA	54778
rs771272246	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59039211	TCAGGTCATCTGCCC[G/T]CCTTGGCCTCCCAAA	54778
rs771315197	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59012732	CTCATGGTGGTTCCA[A/C]CTCTTTTTTTCTTTT	54778
rs771341465	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59091863	AGGAGCATGCAACCT[A/G]GATCCCTCACATGCA	54778
rs771362193	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59028032	GGGTTTCACCATGTT[A/G]GCCAGGCTGGCCTCG	54778
rs771364305	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59069428	GCCAAAAGTCTCATT[G/T]ACAGAATATTTTGTT	54778
rs771381934	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59010881	TTCCTTCTCCTGTTA[G/T]TTAATTGGAATGAAT	54778
rs771425870	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59002460	GCATGGTAAATACGG[G/T]AAGTACGGTTGAGTA	54778
rs771438163	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:58990883	CATTTGAATGTCTTA[G/T]ACCTCTGTTTGTTTC	54778
rs771446947	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59080742	AACTATAATATATAT[A/G]TTGACATAAGATATC	54778
rs771456437	snp	C/T	1.70886e-05	0.00292301	intron-variant	RNF111	GRCh38.p7	15:59067111	TGAGTCAGTCTTTCT[C/T]TCCTGCCCCTCTTGT	54778
rs771464679	snp	A/G	1.68556e-05	0.00290302	intron-variant	RNF111	GRCh38.p7	15:59084261	GTCTGCCTGGTCAGT[A/G]TCTTCTTTAATTTCA	54778
rs771469841	in-del	-/ATTTT			intron-variant	RNF111	GRCh38.p7	15:59029979	TGATTAATATATTTC[-/ATTTT]GAGTCATGATATTTA	54778
rs771500358	snp	C/T	1.6473e-05	0.00286988	missense	RNF111	GRCh38.p7	15:59058473	CTGCTTCAGCTGTCA[C/T]CAGTAGCCAACCTTC	54778
rs771505497	in-del	-/A	0.000129934	0.00805916	intron-variant	RNF111	GRCh38.p7	15:59084094	ACCAATTATTCAATT[-/A]TTTCCAGTGGTCTTT	54778
rs771552472	snp	A/C	1.74711e-05	0.00295554	missense	RNF111	GRCh38.p7	15:59030847	TGGACTCCTGAATAT[A/C]ACGAGCTCTACACCT	54778
rs771583800	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58993783	GTGGATTGTGTTAAC[A/G]TGGAGAAGATTTTTG	54778
rs771591912	snp	A/G	1.65053e-05	0.0028727	missense	RNF111	GRCh38.p7	15:59031415	CGGGATTGTTAATGA[A/G]AAGACCCTGTTTACA	54778
rs771599204	snp	C/T			intron-variant, utr-variant-5-prime	RNF111	GRCh38.p7	15:59004030	AAGAAGTTTGAGTGA[C/T]CTATCCTGTGTTTAT	54778
rs771602654	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59041205	TTGTTCAACCAGTCT[C/T]CTATTGATGAACAGT	54778
rs771613775	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59063133	TTTCTCTTCTTGGCG[C/T]TTAGCTACATGATTG	54778
rs771644600	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59058688	CTTCATATGTTATCA[A/G]GGTAGTCTTTATTAT	54778
rs771657212	in-del	-/TA			intron-variant	RNF111	GRCh38.p7	15:59016164	AAATATATATATGTA[-/TA]TATATATATAGTTTT	54778
rs771681906	snp	A/G	1.65127e-05	0.00287334	missense	RNF111	GRCh38.p7	15:59031499	CCTCACAGAGGACAC[A/G]GAAACAAAAAGAGAG	54778
rs771694687	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59044540	TGTTGTACTACTCAT[A/C]TTCTTTCTGGCCTGG	54778
rs771743107	in-del	-/T	1.65899e-05	0.00288005	frameshift-variant	RNF111	GRCh38.p7	15:59085775	TACAATTAGGAGCTC[-/T]TCCTTTAATGGTAAA	54778
rs771751532	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58996463	GTGCATGCCTGTAAT[C/T]CCAGCTACTTGGGTG	54778
rs771782762	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59094253	TTAAGTTTAATGTGT[A/T]AAGATATTCTTGATA	54778
rs771786646	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59013299	ATCTTACCCATTACA[C/T]GTTTGTCATGACTAA	54778
rs771795724	snp	C/T			intron-variant, utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022484	CTAATCTCCATTTAA[C/T]TGTATTTTCTTTCCT	54778
rs771799552	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59014084	GTGTGAGCCACTGCC[G/T]CCAGCCTCATTTTTA	54778
rs771807265	snp	A/T	1.65236e-05	0.00287429	missense	RNF111	GRCh38.p7	15:59091124	CCAGGGGACAATTGA[A/T]AGATGTACATATCCA	54778
rs771812966	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59066737	TTTCATGATTTGATT[A/T]TTCTGTGCATTTTTT	54778
rs771821761	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58988954	ACTTTATTTCATTTG[A/G]TATTTTATCTATAAT	54778
rs771821899	snp	C/T			missense	RNF111	GRCh38.p7	15:59081142	GCCAGTACAGCTGCA[C/T]CAATCCCTCAGCATC	54778
rs771846840	snp	A/T	1.65326e-05	0.00287507	intron-variant	RNF111	GRCh38.p7	15:59089799	GTTTGTCACAGTATC[A/T]TTAATGCAGATTGAG	54778
rs771867835	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59071563	CTGGGCGTGGGGTCT[C/T]GTGCCTTTAGTTCTA	54778
rs771871144	snp	A/G			utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58987671	GAGCCCTAGTGTCGT[A/G]CTCTCCTCGGTAGGG	54778
rs771874289	snp	A/G			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020658	ACAGATGAGAAAATC[A/G]TTAAGTTCACTGAGA	54778
rs771887034	snp	C/T	8.3013e-05	0.00644202	intron-variant	RNF111	GRCh38.p7	15:59076232	TAAGTATATACTTAG[C/T]GGACACAAAATCTAG	54778
rs771887636	in-del	-/TTT			intron-variant	RNF111	GRCh38.p7	15:59049363	TCCAGGTGTCTTTGA[-/TTT]TTTTTTTTTTTTTTT	54778
rs771902389	in-del	-/T	3.35022e-05	0.00409268	intron-variant	RNF111	GRCh38.p7	15:59052438	AAGCTATCGGTGAGA[-/T]TTTAATTCTTAGTTA	54778
rs771930569	snp	A/C	1.92725e-05	0.00310417	intron-variant	RNF111	GRCh38.p7	15:59030797	AATATCTAATTTTGT[A/C]TTCTAGGCTTTCCTT	54778
rs771930855	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59024394	CTGCCTAGATGAGAT[G/T]CCTGCTTCCTTGGAA	54778
rs771944846	snp	A/G	1.64857e-05	0.00287099	missense	RNF111	GRCh38.p7	15:59076150	CAAGCATGGTTGCGC[A/G]GCCCCAGCCCCAGCC	54778
rs771947865	in-del	-/GG			intron-variant	RNF111	GRCh38.p7	15:59003040	CGCGGGATTGCAGTT[-/GG]CTATTCACAGGTGCT	54778
rs771981148	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59015905	CGCCCAGGTTGGAGT[A/G]CAGTGGCGTGATCTT	54778
rs771987321	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59004823	AAATATCAGAGAAAG[A/G]GTAGGTTTGTGTATA	54778
rs772009039	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59066039	TTTAAGAAGTACATA[C/G]CTGCCTGCATTATGT	54778
rs772011781	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:58990829	ATTTGTTTTTCTTTC[A/C]GAAACCTGTAATTAT	54778
rs772028328	snp	C/G			missense	RNF111	GRCh38.p7	15:59066866	CACCATGTGGAGGGT[C/G]GTCACAGAACCACCA	54778
rs772038824	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59076468	TTCTAGGCACAGTAA[A/T]GTAAATTTTTAAGAA	54778
rs772070929	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59005172	TTCCTCTTACAACTC[A/C]AGTTCTCTTTCTTTA	54778
rs772072663	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59027974	GGGATTACAGGTGCA[C/T]GCCACCATGCCCGGA	54778
rs772075232	snp	A/G	3.29511e-05	0.00405887	synonymous-codon	RNF111	GRCh38.p7	15:59031155	GAATTGTGTTAAAGA[A/G]AACCAGGGAATATTA	54778
rs772087337	snp	A/C	1.64741e-05	0.00286998	missense	RNF111	GRCh38.p7	15:59081143	CCAGTACAGCTGCAC[A/C]AATCCCTCAGCATCT	54778
rs772088723	snp	C/G	0.00027126	0.0116429	intron-variant	RNF111	GRCh38.p7	15:59093504	GCGTAAGCCACTGCA[C/G]TCGGCTATAGCATCT	54778
rs772132642	snp	C/G	1.64866e-05	0.00287106	missense	RNF111	GRCh38.p7	15:59031056	GCAAGAGAAGGAAAT[C/G]AATGGTAACCAGCAA	54778
rs772173200	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59080596	GTGTAAATGAAAGAG[A/T]GAGTGCAGGAGTGAG	54778
rs772175040	snp	C/G	1.7022e-05	0.00291731	intron-variant	RNF111	GRCh38.p7	15:59066760	CATTTTTTTCTGTTT[C/G]AAGATGACTCAAGGA	54778
rs772196819	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59035210	GCCCTGTCCATGACA[C/T]GTGGGAATTATTATA	54778
rs772214579	snp	C/T			downstream-variant-500B	RNF111	GRCh38.p7	15:59097890	CTCTCAAAAAAAAAC[C/T]ACAACTGTTATTTGT	54778
rs772222469	snp	C/G			utr-variant-3-prime	RNF111	GRCh38.p7	15:59097228	AAAATGAACATTTCA[C/G]TGGTAGCTGTCCAAA	54778
rs772224622	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59007374	TAGCATGATATTTTT[A/G]AGATTAATCCGTATT	54778
rs772256288	snp	A/G			missense	RNF111	GRCh38.p7	15:59052325	ATTGATGAAGATGTT[A/G]TGGTGATAGAAGCTT	54778
rs772288133	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58990385	AAGCTGTGGGCCAGG[C/T]GTGGTGGCTCACCCC	54778
rs772306452	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59054196	CCCGCCTCGGCCTCC[C/G]AAAGTGCTAGGATTA	54778
rs772329069	snp	C/T	3.29582e-05	0.00405931	missense	RNF111	GRCh38.p7	15:59081223	CCAGCACAGAGACTG[C/T]ATCCTCATGAAGTGA	54778
rs772329089	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59068262	AAAGATGTAATTTCA[A/G]AGAAAAATTGTAATT	54778
rs772344441	in-del	-/C			intron-variant	RNF111	GRCh38.p7	15:59054641	AACTTTATACTCCTT[-/C]TTAAGAATTTTATTT	54778
rs772364671	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59036868	GACAGTCTTATCTGT[G/T]GTCCAGGTTGGAGTG	54778
rs772370425	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59001661	AGCTAGGTTCTTTAA[C/T]AGAAAATACTTAATA	54778
rs772373427	snp	A/G/T	0.000921985	0.0214513	intron-variant	RNF111	GRCh38.p7	15:59052464	AGTTAAATGTTTGAA[A/G/T]TATTAAATATAAATA	54778
rs772428863	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59056900	GGAGAAGGTGATAGA[C/G]TAGCCTTTTCCACAT	54778
rs772430959	in-del	-/CTT			intron-variant	RNF111	GRCh38.p7	15:59079355	TACTGAGCTTTGTGC[-/CTT]CTTGAAGAGTAAAGC	54778
rs772436584	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59061678	CCTTTATCTGTGCTC[C/T]ACCTCTTATCCTTTC	54778
rs772458168	in-del	-/TATAT			intron-variant	RNF111	GRCh38.p7	15:59075668	ACAAAAAGATTTTAA[-/TATAT]TAAACTTTTGTTCAT	54778
rs772502741	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59089528	CAGAATGCTTAGTTG[G/T]AGTTATGTATTCTTA	54778
rs772521694	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59048523	TGTTCTTAAACTGGA[C/T]TGTGGTGATGATTAC	54778
rs772528498	snp	C/T	1.64874e-05	0.00287113	missense	RNF111	GRCh38.p7	15:59085720	GGTGCATTGCATCCT[C/T]ACTTGGCCCATTATC	54778
rs772530722	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59079537	CCTTGCTGAATGAAT[C/G]AAAAGCATTAAAAAT	54778
rs772548906	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:58991075	CCGAGGCGGGTAGAT[C/G]ATGAGGTCGGGTTCG	54778
rs772570364	snp	A/G	1.85135e-05	0.00304244	missense	RNF111	GRCh38.p7	15:59092600	ACAGAGGAAAAATGT[A/G]CTATCTGTTTGTCTA	54778
rs772613385	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59090423	TTAGTAGAGATAGTG[C/T]TTTGCCATGTTGGCC	54778
rs772635205	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59062805	TCTACTTTTCCCCTT[G/T]ATGCCAAGATTTCTC	54778
rs772642255	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59020138	AAATACATATTTTAT[A/G]TATGTTAGATATATA	54778
rs772656603	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59047750	CCAGGTAATTTTTGT[C/G]TTTTTTGTAGAGACA	54778
rs772685123	snp	A/T	1.66183e-05	0.00288251	missense	RNF111	GRCh38.p7	15:59055816	GGCAGAATGCAGCAG[A/T]AGTTGTGGACCTTAC	54778
rs772723719	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59089563	AGTCAAATTTTATGA[A/G]CAGTTGAATTGAAAA	54778
rs772755163	snp	A/G			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021237	CTCACTGCAAACTCC[A/G]CCTCGTGAGTTCAAG	54778
rs772757327	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59008642	TTACACCAATAGCCC[C/T]AGTGTTGATACAATT	54778
rs772775053	snp	A/T	1.64749e-05	0.00287005	synonymous-codon	RNF111	GRCh38.p7	15:59031197	ACACCTAGGGACACC[A/T]AGTGATGAAGATAAT	54778
rs772804237	in-del	-/GCTTTG			intron-variant	RNF111	GRCh38.p7	15:59005557	GTTACTCCAACCTTT[-/GCTTTG]GCCTTTAACAACTCA	54778
rs772807682	snp	A/G/T	0.000501002	0.0158193	intron-variant, missense	RNF111	GRCh38.p7	15:59004167	AGTTCTGGATTAGCA[A/G/T]TTTTAAGGTCTCAAC	54778
rs772822858	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59072558	TCCCAGGTTCATGCC[A/G]TTCTGCCTCAGCCTC	54778
rs772840011	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59039487	TGAGTATCATTATGA[A/G]TGCATGAATTTTAGT	54778
rs772844636	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59002823	ACCTGTTAGGCATAT[G/T]CCTGTCACATAGTCT	54778
rs772856000	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59029168	TATATGAGGGTTCCA[A/G]TGTTTTTTTTTTATG	54778
rs772900579	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59003483	TGCTTACTGCAACCT[C/T]CACCTCCTAGGCTCA	54778
rs772907398	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58992827	CCTATCTCAAAATAA[A/G]TAAGTAAATGAAATA	54778
rs772923180	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59061774	TTCCTTAGTACATGC[A/T]CATGTACACTTGTTT	54778
rs772952861	snp	A/G	1.6631e-05	0.00288362	intron-variant	RNF111	GRCh38.p7	15:59058329	AATTTGTTTTGAAAT[A/G]CTAAGTTGACATTTT	54778
rs772959648	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59053966	TTTGAGACAGAGTCT[C/G]CCTCTGTCACCCAGG	54778
rs772964264	in-del	-/TA			intron-variant	RNF111	GRCh38.p7	15:59016163	AAAAATATATATATG[-/TA]TATATATATAGTTTT	54778
rs772998052	snp	C/G/T			intron-variant	RNF111	GRCh38.p7	15:59094358	AATGTTTTTGAGAGA[C/G/T]AATTAAATGATGTAA	54778
rs773038114	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59012352	TCCACTTAGGTAATT[A/G]CAGTATTTGATAATT	54778
rs773047418	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59055384	TTTAGCTATTAACAG[A/G]AAATGTAAATAGTTT	54778
rs773049569	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59041209	TCAACCAGTCTCCTA[C/T]TGATGAACAGTTTGC	54778
rs773049979	snp	C/G	1.64738e-05	0.00286995	missense	RNF111	GRCh38.p7	15:59094892	GCCCAGCTGCCAAGT[C/G]AAAGTTGACACCATG	54778
rs773066031	snp	A/G	0.000164948	0.00908003	synonymous-codon	RNF111	GRCh38.p7	15:59085740	GGCCCATTATCACGC[A/G]CCTCCTCGACTTCAT	54778
rs773111264	snp	A/G	5.22826e-05	0.00511259	intron-variant	RNF111	GRCh38.p7	15:59066744	ATTTGATTATTCTGT[A/G]CATTTTTTTCTGTTT	54778
rs773153792	snp	A/G	1.64879e-05	0.00287118	missense	RNF111	GRCh38.p7	15:59075976	TGCCAGTGGACCTGA[A/G]CAACAGTGGTATCAG	54778
rs773155768	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59062085	TCCCCGAGACAGGGT[C/G]TTGCTTTGTCACGTA	54778
rs773164080	in-del	-/TTTTTTTC	0.000757289	0.019444	intron-variant	RNF111	GRCh38.p7	15:59093354	TTTTTTTTTTTTTTT[-/TTTTTTTC]TTTTTTTCCTTTTCT	54778
rs773173026	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59086745	TCCAAGTAAGCTGGT[A/G]TTTCTAATTTTAGGA	54778
rs773177792	snp	C/G			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986268	GTCGCCCAGGCTGGA[C/G]TGCAGTGGCACAATC	54778
rs773182544	snp	A/G	3.64159e-05	0.00426692	intron-variant	RNF111	GRCh38.p7	15:59085822	ATTTTGACATGTTCT[A/G]AAAGTTCCTTTTCTA	54778
rs773203155	snp	A/C	1.65138e-05	0.00287343	missense	RNF111	GRCh38.p7	15:59031609	GAGAATGACCTCAGC[A/C]GTGAATCCTCTTCTA	54778
rs773235782	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59017055	TGATTCTATATTACG[A/G]TGAATTGTATAATAT	54778
rs773251781	snp	A/G	1.64814e-05	0.00287061	missense	RNF111	GRCh38.p7	15:59052320	GAAGTATTGATGAAG[A/G]TGTTGTGGTGATAGA	54778
rs773281744	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59024847	CTCCCCCTCCCTCAG[A/G]TCCTCGCAACCACCA	54778
rs773284621	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59073924	TGGATGTTGTGTTAG[C/G]TATGAAAACATTAAT	54778
rs773298118	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59024698	TTAAATGTACGTAAC[A/G]TAAAATTACCATTTT	54778
rs773342573	snp	A/G	1.83869e-05	0.00303202	utr-variant-5-prime, missense	RNF111	GRCh38.p7	15:59030815	CTAGGCTTTCCTTAA[A/G]GTTTCCCATGTCTCA	54778
rs773414615	snp	A/G	1.66369e-05	0.00288412	intron-variant	RNF111	GRCh38.p7	15:59091012	ACAGTTCTGTTCAAG[A/G]AATAATCATCTTGGC	54778
rs773419849	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59027066	TTAATTGTGCTGTGA[A/G]TTGCTTCTTTGTAAA	54778
rs773429284	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59079539	TTGCTGAATGAATCA[A/G]AAGCATTAAAAATTG	54778
rs773452425	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59012531	GCATGATTGCTGAAC[A/G]TTTTAACACAAGAAA	54778
rs773590004	snp	A/G	1.6646e-05	0.00288491	intron-variant	RNF111	GRCh38.p7	15:59076246	GTGGACACAAAATCT[A/G]GAGTCATGTCAATGA	54778
rs773592730	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59059774	ACTAACTTTCTTTCA[-/T]TTTTTGGATAATGGT	54778
rs773600538	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59057974	TATTGTGTCAGACAG[C/T]GTGGTTTGTAACACT	54778
rs773618200	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59026156	TCATACCAATAATAG[C/T]GTATCACAGTTTAGA	54778
rs773619902	snp	A/T	1.65592e-05	0.00287738	missense	RNF111	GRCh38.p7	15:59081268	GTTCAAAGGAGGAGG[A/T]TGATGCAGCATCCAA	54778
rs773621519	snp	A/G	6.58913e-05	0.00573945	missense	RNF111	GRCh38.p7	15:59067012	GATCCTGCTTGCCCT[A/G]TGGAAAGACCTCCAC	54778
rs773623252	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59049930	TGTTTTTAGTAGAGA[C/T]GGAGTTTTACCATGT	54778
rs773675443	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59090548	GTTGTGTTTTTTTTA[C/T]GTCAGTTTGGAAGTT	54778
rs773709980	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59048552	ACACTCCATAAATTT[A/C]CTAAAATTAGCAAAA	54778
rs773713322	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59070718	TTGAGTATCATCACA[C/T]CCCTTTCCTTTCAGC	54778
rs773736858	snp	A/G	1.69668e-05	0.00291258	intron-variant	RNF111	GRCh38.p7	15:59031717	GGTAAAAATGTTTAA[A/G]CTGAGTAAAACATGG	54778
rs773756783	snp	C/T			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021253	CCTCGTGAGTTCAAG[C/T]GATTCTCCTGTCTCA	54778
rs773801560	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59036904	GTGCAATTATGACTC[A/G]CTGCAGCCTCAACCT	54778
rs773804380	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59003396	AGGTGTGAGCCGCCA[C/T]ACCCGGCCTTTTTCT	54778
rs773820641	snp	G/T	1.65351e-05	0.00287528	intron-variant	RNF111	GRCh38.p7	15:59058349	GTTGACATTTTGTAT[G/T]TTGTAGAACCTACTG	54778
rs773855050	in-del	-/TATTT			intron-variant	RNF111	GRCh38.p7	15:58992042	AAATGTCTGGTATTT[-/TATTT]TATTTTATTTTATTT	54778
rs773862009	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59009802	TCTGCAAAAAATTCA[A/G]AAAATTAGCTGGGCA	54778
rs773866281	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58999713	TAAGGGTATTAGTTC[A/G]TTCTCACACTGCTAT	54778
rs773891046	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58993542	GACTCCATCTCAAAA[C/T]TTGTGAAAGTACCAT	54778
rs773897096	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59041120	AAAGTATATATCTCC[A/G]TATATCTCATTTCTT	54778
rs773982097	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59012236	GTTGGCCAGGCTGGT[C/G]TCGAACTTCTGACCT	54778
rs773990131	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59018286	ATTCAAATCTGCTAA[A/C]GGTCACTGCCATTTC	54778
rs773997225	snp	A/C	1.6715e-05	0.00289089	missense	RNF111	GRCh38.p7	15:59031691	ACCAAAACAATCCAG[A/C]TGTTCCCTCAGGTAA	54778
rs774005627	snp	C/T	5.93548e-05	0.00544737	intron-variant	RNF111	GRCh38.p7	15:59085834	TCTAAAAGTTCCTTT[C/T]CTAAGTATTTTATTG	54778
rs774006330	snp	C/G			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59020598	GTTGATGTTATGTTT[C/G]TCTTTGATGACTAAT	54778
rs774043217	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59029017	ACTCCTGGCCTCCAG[C/T]GATCCGCCCGCCTTG	54778
rs774043225	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:58994750	CCCAAAGTGCTGGGG[G/T]GAGCCTTTGCGCCTG	54778
rs774051593	in-del	-/G			intron-variant	RNF111	GRCh38.p7	15:59080775	AGATTATTGTAAGAA[-/G]GGAGCAAGTTGCTTG	54778
rs774060053	snp	C/T	1.64999e-05	0.00287222	missense	RNF111	GRCh38.p7	15:59031400	AGACAGAATCTGTAT[C/T]GGGATTGTTAATGAA	54778
rs774068166	in-del	-/A	1.64806e-05	0.00287054	frameshift-variant	RNF111	GRCh38.p7	15:59052381	GAAGAAATTAATGTT[-/A]ACCTCAACTGACAGT	54778
rs774126159	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59004424	TTACTATTTTTATCT[-/A]AGAATATGAAATTTG	54778
rs774150663	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59033383	GCCATGTTCAGATCA[C/G]TTTTACCTACACAAA	54778
rs774175613	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59011417	GGGGCATTCTAGCAC[A/G]TTTAAGGTACTCAGA	54778
rs774185854	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59041356	GTCAGGAATTCAAGA[C/G]CAGCCCGACCAACAT	54778
rs774196936	snp	A/G	1.83407e-05	0.0030282	intron-variant	RNF111	GRCh38.p7	15:59084094	ACCAATTATTCAATT[A/G]TTTCCAGTGGTCTTT	54778
rs774208427	snp	A/G	1.64754e-05	0.00287009	missense	RNF111	GRCh38.p7	15:59076068	TCCTCCCGAGCTGCA[A/G]TCTTTGGCCATCAGG	54778
rs774211898	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58996391	CATCCTGGCCAACCT[A/G]ATGAAACCCTGTCTC	54778
rs774221479	snp	A/T			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986114	ATTGAGGAAAATCCT[A/T]GTCGAATGCTCTTTT	54778
rs774226912	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59075066	TGCCTAAAGCAATTA[A/T]AATAGTAACATCAAT	54778
rs774227049	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59063132	GTTTCTCTTCTTGGC[A/G]CTTAGCTACATGATT	54778
rs774239012	in-del	-/AA			intron-variant	RNF111	GRCh38.p7	15:58989358	TTCTTGCCATTTAAC[-/AA]CTTGGACAAATGACT	54778
rs774261973	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59053040	GATGTTGAAATAGCC[C/T]TTTCTGTTAGAATCT	54778
rs774274609	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59089821	CAGATTGAGTATATA[C/T]ATACTACTATACACA	54778
rs774280635	snp	A/G	3.3018e-05	0.00406299	intron-variant	RNF111	GRCh38.p7	15:59089780	TAATAAAATAAATGA[A/G]TATGTTTGTCACAGT	54778
rs774289663	snp	A/G	3.33673e-05	0.00408442	intron-variant	RNF111	GRCh38.p7	15:59076254	AAAATCTAGAGTCAT[A/G]TCAATGAAGCATTTT	54778
rs774298553	snp	A/G	3.37064e-05	0.00410512	missense	RNF111	GRCh38.p7	15:59055837	TGGACCTTACCGTTG[A/G]TGAAGATGGTAAATT	54778
rs774311308	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:58995209	TGTTTCTTGCCTATG[C/G]TGATCTTTACTGATC	54778
rs774328927	in-del	-/CT			intron-variant	RNF111	GRCh38.p7	15:58995460	TCTTTTTAACATAAC[-/CT]CTTGTTTTTTTTTTT	54778
rs774343564	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58990376	CCTGTCATGAAGCTG[C/T]GGGCCAGGCGTGGTG	54778
rs774344649	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59092821	CAACATAACAAGACT[C/G]TGTTTCTACAAAAAA	54778
rs774353166	snp	A/C			utr-variant-3-prime	RNF111	GRCh38.p7	15:59097129	ATAAGTAATGAAGAA[A/C]GTAAGGAAGAAAATG	54778
rs774394311	snp	C/T	8.243e-05	0.00641936	missense	RNF111	GRCh38.p7	15:59030950	TGCATCCAGAGCCCA[C/T]TGGGGCAGCCAAAAG	54778
rs774401959	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58999625	ACAGGTGTCAGCCAC[C/T]GTGCCCGGCCTATTA	54778
rs774423808	snp	C/G			utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096245	TTCATATACAGGATA[C/G]CCTAATTTTATTTGT	54778
rs774427237	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59084661	TTTTGAAATAAACGG[C/T]ACGTTATTCTTCACT	54778
rs774430965	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59025359	TTTTAGTACGAGCTA[A/T]TGCACTTGAGGGTCC	54778
rs774474946	snp	A/G	1.81691e-05	0.003014	missense	RNF111	GRCh38.p7	15:59092564	TGCAAACAAGATGGG[A/G]AAGAAGGGACTGAGG	54778
rs774483693	snp	A/G	1.64857e-05	0.00287099	missense	RNF111	GRCh38.p7	15:59031030	TCTCACCTGTGTGAT[A/G]ATTCTCAAAAGCAAG	54778
rs774524194	in-del	-/TG			intron-variant	RNF111	GRCh38.p7	15:59003104	CTCAAGTGATCCTAC[-/TG]CCTGTTTAATTTTCT	54778
rs774547321	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59049501	CTGGTGCTTCAGTTG[C/T]ACCTAGGTACCTTTC	54778
rs774549529	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59036783	GACCCAACAGTTGTA[C/T]ATAATTAACTGACTT	54778
rs774566257	snp	A/G	1.65053e-05	0.0028727	synonymous-codon	RNF111	GRCh38.p7	15:59080994	CCCGCATTCTCATGG[A/G]AACCCCCCTCCTCAG	54778
rs774566670	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59089429	ATTTTACTCTTTTCA[A/G]GTTTGAGCTACTAAG	54778
rs774600775	in-del	-/TACT			intron-variant	RNF111	GRCh38.p7	15:58991003	ATATTTAAAGACAAA[-/TACT]TAGCTGAGGCTGGGT	54778
rs774610752	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58989390	TATCATCTCTCTCCT[A/G]CTCATTTGTTTGTGA	54778
rs774621984	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59047713	CCCAAGTATCTGGGA[C/G]TACAGGCATGTGCTA	54778
rs774632825	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59056723	ACTGTTTGCATTTCA[C/T]TCAACAATCTCTTGG	54778
rs774639547	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59025137	CGATCCGCCCTCCTC[C/T]GCCTCCCAAAGTGCA	54778
rs774646017	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59026058	TCTTTTAAAATCTTA[C/T]TTCTTTAGAGTCATG	54778
rs774666852	snp	A/C	1.71428e-05	0.00292765	intron-variant	RNF111	GRCh38.p7	15:59067113	AGTCAGTCTTTCTTT[A/C]CTGCCCCTCTTGTCT	54778
rs774688870	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59000602	ATAATCCTAGCTATT[C/T]GGGAGGCTGAGGCAC	54778
rs774737102	snp	C/G	1.65787e-05	0.00287907	intron-variant	RNF111	GRCh38.p7	15:59058578	GTGGGGGAGGGGAGA[C/G]TTTTTGTCATTACTT	54778
rs774741350	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59072665	CACCGTGATAGCCAC[A/G]TTGGTCTCAATCTCC	54778
rs774745481	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59035471	AGATGCAATGAGGGT[A/C]CAGATGTTGGGTAAT	54778
rs774747701	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59048382	ACTTAACATAAAACT[A/T]TACAAAATCCAAACC	54778
rs774752596	snp	A/T	3.45459e-05	0.00415593	intron-variant	RNF111	GRCh38.p7	15:59052449	GAGATTTTAATTCTT[A/T]GTTAAATGTTTGAAA	54778
rs774769225	snp	C/T	4.99954e-05	0.00499952	intron-variant	RNF111	GRCh38.p7	15:59091168	AGGTAAGAATTTATT[C/T]TATGAAACTTCTGGA	54778
rs774774479	snp	A/C	1.64741e-05	0.00286998	missense	RNF111	GRCh38.p7	15:59067025	CTGTGGAAAGACCTC[A/C]ACAAGTACAAGCACC	54778
rs774814965	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58992726	TCGGGAGGCTGAGGT[A/G]AGAGGATGGCTTGAG	54778
rs774826066	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59001923	ACATTAATAGCAATA[A/G]CTAATAAAAAAATTT	54778
rs774829987	in-del	-/AAAAC			intron-variant	RNF111	GRCh38.p7	15:59060449	TCTCTTTTGAAGAAA[-/AAAAC]AAAACAAAACAAAAA	54778
rs774868439	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59060377	TGGGAGGCCAGGGAC[A/G]CAGATCACTCGAGGC	54778
rs774872381	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59047683	CAGGCTCAAGCTGTC[G/T]TCCTACCTCAGCCTC	54778
rs774923707	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59007385	TTTTGAGATTAATCC[A/G]TATTGATACATGTAT	54778
rs774929605	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59012110	TGTAACCTCCGCCTC[C/T]TGAGTTCAGGTGATT	54778
rs774950954	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59064072	AATTTATAGGAAACA[A/G]TTACTTAATGTTGGG	54778
rs774984840	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59069560	CAGTGTAAAATAAAT[A/G]TAACTCGTTTACCCA	54778
rs775014685	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59019823	AATTAGCCAGGTGTG[A/G]TGGTGTGTGCCTATA	54778
rs775040842	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59058882	ATTAAAGGATATTAT[C/T]AAGACAGTGAAAGAC	54778
rs775046252	snp	A/G	1.65108e-05	0.00287317	synonymous-codon	RNF111	GRCh38.p7	15:59031503	ACAGAGGACACAGAA[A/G]CAAAAAGAGAGGATA	54778
rs775054846	snp	C/G	1.7117e-05	0.00292544	missense, intron-variant	RNF111	GRCh38.p7	15:59084106	ATTATTTCCAGTGGT[C/G]TTTTTGTGTTCTGTG	54778
rs775082540	snp	C/G/T	3.49546e-05	0.00418044	intron-variant	RNF111	GRCh38.p7	15:59092684	ATTGTCAAAACTGTA[C/G/T]ATGGGATTTTATTTG	54778
rs775096145	snp	A/T	1.91195e-05	0.00309183	intron-variant	RNF111	GRCh38.p7	15:59030799	TATCTAATTTTGTCT[A/T]CTAGGCTTTCCTTAA	54778
rs775109570	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59022619	GTTTCTGTGGATATC[A/T]GTTAAGGTTAAGGAG	54778
rs775154724	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59050526	CTCTATATCAAAGGG[A/G]TTGAATAGTTTCAAA	54778
rs775184734	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59039546	TCTTTTTATACTTTT[C/T]TAAATGATTTCATCT	54778
rs775190872	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59034746	GGCAAAAAGTCTTAG[C/T]TAATTCAAATTGGTA	54778
rs775219414	in-del	-/T	5.28229e-05	0.00513894	intron-variant	RNF111	GRCh38.p7	15:59085808	GGAAAATTTTCAAAA[-/T]TTTGACATGTTCTAA	54778
rs775220202	in-del	-/CTT			intron-variant	RNF111	GRCh38.p7	15:58989539	CAGATCCTTCTGTCA[-/CTT]CTTAACTTTTGTTTG	54778
rs775220929	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59043610	GTTTTGAATGGTTTC[C/T]GGTATTTGCTATTGT	54778
rs775264301	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59015805	GTCCTTAATTGCCTC[A/G]TTTTGTTCCTACAGA	54778
rs775299767	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59090231	GTTTGTTTGTTTGTT[-/T]GTTGTTGTTGTTTTT	54778
rs775309466	in-del	-/TTGA	1.69977e-05	0.00291523	intron-variant	RNF111	GRCh38.p7	15:59052445	GGTGAGATTTTAATT[-/TTGA]CTTAGTTAAATGTTT	54778
rs775309580	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59038733	TGGCATCATTTCTGT[A/G]AACTGGTAGGTAGTT	54778
rs775362675	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58995140	GCTCCTCATCAGATC[A/G]TCCTGTTCCTCATCA	54778
rs775385993	in-del	-/CT			intron-variant	RNF111	GRCh38.p7	15:59032891	TCATGCGTGCTGACT[-/CT]CTCTCTCTCTCTCTC	54778
rs775403876	snp	A/T	0.000115486	0.007598	missense	RNF111	GRCh38.p7	15:59031397	CTGAGACAGAATCTG[A/T]ATCGGGATTGTTAAT	54778
rs775410767	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59079851	TTCACCTTAATGTAG[C/T]ACAGGAATAATGACA	54778
rs775419235	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59062954	CATCACCTCCCTTCC[A/G]ATTGTAACAACCAAA	54778
rs775436937	snp	A/G	0.000680289	0.0184305	missense	RNF111	GRCh38.p7	15:59031346	TGAATGCTAAAAGTA[A/G]AAGCCATAGTGCACG	54778
rs775444330	in-del	-/TTT			intron-variant	RNF111	GRCh38.p7	15:59041959	TGATCAGTCTGTTCA[-/TTT]TATTTTTTTTTTTTT	54778
rs775493353	in-del	-/TTT			intron-variant	RNF111	GRCh38.p7	15:59060807	TTATTATTATTATTA[-/TTT]TTTTTTTTTTTGTGA	54778
rs775520269	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59035160	CATGAGAACATGGTA[C/T]GTGGGAAACTGCCCC	54778
rs775542640	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59004342	ATTCTGAAGATTGCA[A/G]AAAAGTATATAGGTA	54778
rs775550623	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59007330	CAAATAAATAGAAGC[A/G]TACCGATACTTTGTG	54778
rs775559056	in-del	-/TTT			intron-variant	RNF111	GRCh38.p7	15:59090229	TTGTTTGTTTGTTTG[-/TTT]GTTGTTGTTGTTTTT	54778
rs775598654	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59094445	ATTTGATTTTTAAAA[A/T]TATATTTGCAATATT	54778
rs775599053	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59015625	TTATTCTCCCCTACT[-/A]AAAAAAAAAAAAGAA	54778
rs775613225	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59066297	ACTGCATAAAATCAT[A/G]TGATGTATATGTTAA	54778
rs775630603	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58994367	TTTTGACATAATTTC[A/G]AACTTACCGAAAGAT	54778
rs775630806	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59005120	TTCAGTATGCCTATA[A/C]TGTCAGCCATTAAAG	54778
rs775637708	snp	C/T	1.64738e-05	0.00286995	missense	RNF111	GRCh38.p7	15:59081149	CAGCTGCACCAATCC[C/T]TCAGCATCTTCCTCC	54778
rs775676552	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59025129	TGCTGTTACGATCCG[C/T]CCTCCTCCGCCTCCC	54778
rs775694300	snp	A/G			missense	RNF111	GRCh38.p7	15:59031006	AATAGTAAAGTGGGG[A/G]ATGAATTCTCTCACC	54778
rs775771288	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59046300	CAGGGCTAAGGTGAT[A/C]CTCCCACGTCAGCCT	54778
rs775782411	in-del	-/TTTTTTTTT			intron-variant	RNF111	GRCh38.p7	15:59017754	TTATTTGTTGAACTC[-/TTTTTTTTT]TTTTTTTTTTTTGAG	54778
rs775783119	in-del	-/AGTG			intron-variant	RNF111	GRCh38.p7	15:59004993	TCTAGGCATATAATC[-/AGTG]AGCAGAAGGGCAAGC	54778
rs775801051	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59035417	AAGGCAAGTCCCTTC[C/T]GCATATGAGCCTGTA	54778
rs775814407	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59076624	CAGCACTTTGGGAGG[C/T]CAAGGCAGGAGGATG	54778
rs775842706	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58991033	GGGTGCGCTTGCTCA[C/T]ACCTGTAATCCCAGC	54778
rs775865246	snp	A/T	3.29674e-05	0.00405988	missense	RNF111	GRCh38.p7	15:59031058	AAGAGAAGGAAATGA[A/T]TGGTAACCAGCAAGA	54778
rs775882190	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59090059	AAATGTGGTGGGGAA[C/T]GGAATGTTTTTGACT	54778
rs775882906	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59006675	CCTGTTGCTTTTTAT[G/T]CATTTTAAAGTTACA	54778
rs775888089	snp	A/G	3.30666e-05	0.00406598	missense	RNF111	GRCh38.p7	15:59031624	AGTGAATCCTCTTCT[A/G]GCTCATCAACTGAAG	54778
rs775914102	snp	C/G	1.648e-05	0.0028705	missense	RNF111	GRCh38.p7	15:59081011	ACCCCCCTCCTCAGA[C/G]TCAGCCTCCGCCTCA	54778
rs775933684	snp	C/T	1.87714e-05	0.00306355	synonymous-codon	RNF111	GRCh38.p7	15:59092605	GGAAAAATGTACTAT[C/T]TGTTTGTCTATTTTA	54778
rs775963233	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59009842	ATGTCTCTAGTCCCA[G/T]TTACCTGGGAGGCTG	54778
rs775965451	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59069719	GAGACTCATGTTGAT[G/T]TTTGTAGGACTCTAA	54778
rs775990258	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59087106	AAGTTGAATGTCCAA[C/T]AGGAAGTTAAGCCTG	54778
rs775995280	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59073008	AGACTCTGTCTCTAC[-/A]AAAAAATCTAAAAAT	54778
rs775998043	snp	A/C/G/T	0.000115465	0.00759753	missense	RNF111	GRCh38.p7	15:59085738	TTGGCCCATTATCAC[A/C/G/T]CACCTCCTCGACTTC	54778
rs776008637	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59087990	GAAAACATGGAGACA[A/G]TGAATATAGCCTTCT	54778
rs776023425	snp	A/G	0.00178041	0.0297832	intron-variant	RNF111	GRCh38.p7	15:59093507	TAAGCCACTGCACTC[A/G]GCTATAGCATCTTTT	54778
rs776030340	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59002621	TTTAGATCCAGGCTT[C/T]GCTATCAGGTCTTAG	54778
rs776077215	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59017220	AAAAGGTTGGAAACC[A/G]CTGCTGTGTAGGCCA	54778
rs776085988	snp	G/T	1.65509e-05	0.00287666	missense	RNF111	GRCh38.p7	15:59075957	CTTTTTATCTAGCAG[G/T]CATTGCCAGTGGACC	54778
rs776087697	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59061717	TTAACCTTGCTTTAA[A/C]TGTTATCTTCCTTGT	54778
rs776098064	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59073620	TCTTGCTGTCTTCAC[A/G]ACATCTGTAGTTACT	54778
rs776131578	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59015469	TAAAACTACTCTTTG[C/T]CCCCATCACTGTAAG	54778
rs776133198	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59028183	AGCCCTAGGTAACCA[C/T]ATTCTATCTATGTAG	54778
rs776134644	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:58991693	CGGCAAATGCATTAG[G/T]TGAGGTTTGATTCTA	54778
rs776151667	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:58991080	GCGGGTAGATCATGA[C/G]GTCGGGTTCGAGAGC	54778
rs776175671	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59037553	TTAAAATTAATAGGT[A/G]TTGCCGGGCGTGGTG	54778
rs776195961	snp	C/T	2.0177e-05	0.00317617	intron-variant	RNF111	GRCh38.p7	15:59067126	TTCCTGCCCCTCTTG[C/T]CTCTCTCTCTCTCTC	54778
rs776246182	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59062836	AACCTTGGCACTACT[A/G]TTGACTTTGGGCCAG	54778
rs776248347	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59048848	ACCCCAGCACTTTGG[G/T]GGACTGAGGTGGGAG	54778
rs776329957	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59013256	AGAGTTCCCATATAT[C/T]GCTCACTCAGTTACC	54778
rs776336407	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59050407	TGAATTATTGGAAGA[C/T]GGTGGTTTCTGGCGA	54778
rs776343160	in-del	-/TTTCTTTTTT			intron-variant	RNF111	GRCh38.p7	15:58996646	AAAACTCATCAGTAC[-/TTTCTTTTTT]TTTTTTTTTTTTTTT	54778
rs776343594	snp	C/T	1.65143e-05	0.00287348	synonymous-codon	RNF111	GRCh38.p7	15:59031434	ACCCTGTTTACATGG[C/T]AGTTCGTTACGGAGA	54778
rs776369709	snp	A/C/G	3.56165e-05	0.00421986	synonymous-codon	RNF111	GRCh38.p7	15:59055694	AAGGTCTCGTTCAAC[A/C/G]CTTGGACACTCCAGA	54778
rs776377062	snp	A/G	1.64776e-05	0.00287028	missense	RNF111	GRCh38.p7	15:59076042	CATTTGACCCCTGCT[A/G]CCCTGTTTCTTCCTC	54778
rs776382860	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59081454	GTTTGAGTCCATCTG[A/G]GCAACACAGTGAAAT	54778
rs776399222	in-del	-/TTTTTTTT			intron-variant	RNF111	GRCh38.p7	15:59017755	TATTTGTTGAACTCT[-/TTTTTTTT]TTTTTTTTTTTTGAG	54778
rs776416397	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59026025	GTGAGCCACTGTGCC[C/T]GGCCGGCTTTTTTTT	54778
rs776417149	in-del	-/AACTC			intron-variant	RNF111	GRCh38.p7	15:59057587	AGTTCTTTGAAACTT[-/AACTC]ACTCATAAGTTGAAG	54778
rs776436923	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59003641	TCCTGAGCTCAAGCG[A/G]TCTGCCTGCCTCAGC	54778
rs776444468	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:58993368	CAAAAATAAAAAAAA[-/T]TATAACTGTAAATAC	54778
rs776461113	snp	A/C/G	9.88866e-05	0.00703097	missense	RNF111	GRCh38.p7	15:59031090	CAAGAAAAAAGTCTC[A/C/G]TTGTGAGGAAAAAAC	54778
rs776470992	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59083591	CCTAGGTGTGTTAAC[-/T]TGTATTACATGTGTT	54778
rs776516997	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59004251	TTCTCTCCCAATTAT[A/C]TTTACTGATCCTTAG	54778
rs776535736	snp	C/T	1.65745e-05	0.00287871	missense	RNF111	GRCh38.p7	15:59080981	AAGCTTCTGCCTGCC[C/T]GCATTCTCATGGAAA	54778
rs776536752	in-del	-/GGCGGC			utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58987699	GGGAGGAATTGGTTA[-/GGCGGC]GGCGGCGGCGGCGGC	54778
rs776545454	snp	A/C/G	4.96679e-05	0.00498316	intron-variant	RNF111	GRCh38.p7	15:59058571	TAAAAAAGTGGGGGA[A/C/G]GGGAGACTTTTTGTC	54778
rs776557675	in-del	-/T	1.65304e-05	0.00287488	intron-variant	RNF111	GRCh38.p7	15:59091053	CATTATATTCTTCAC[-/T]TTCAGGAACTGATTC	54778
rs776575473	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59076475	CACAGTAAAGTAAAT[C/T]TTTAAGAATTCTCAA	54778
rs776585022	snp	C/G			utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096084	TTCATACATTACCAA[C/G]AGTCGATCACTGATT	54778
rs776614110	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59070702	TTTTCTCTTTCCCAA[C/T]TTGAGTATCATCACA	54778
rs776631364	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59023108	AAAAAATTAACTGGG[C/T]ATGGTGGTGCGTGTC	54778
rs776642384	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59007144	TAAGTTTTGCCAAAT[C/G]CATCTATTTATTGCC	54778
rs776656500	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:58987698	AGGGGAGGAATTGGT[C/T]AGGCGGCGGCGGCGG	54778
rs776657425	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59044895	ATGTTGCCTGTTGTG[A/C]ATATGCTTTAGTTAT	54778
rs776694597	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59013570	GAGTACATGGTGTCA[A/G]CATGACTTAGCACTG	54778
rs776714791	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59014194	AGCTTGGTTCCAGTG[C/T]CCTGTTTGACATGCC	54778
rs776718645	snp	C/T	1.6806e-05	0.00289875	intron-variant	RNF111	GRCh38.p7	15:59052283	GAAGATGCCTTTAAA[C/T]GTTTTTTCTTTTTGT	54778
rs776826324	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59007728	TAATGGTATATTACT[A/G]TAGTTTTAATTTGCA	54778
rs776829913	snp	C/T	1.67928e-05	0.0028976	missense	RNF111	GRCh38.p7	15:59031700	ATCCAGCTGTTCCCT[C/T]AGGTAAAAATGTTTA	54778
rs776847382	snp	C/G			upstream-variant-2KB	RNF111	GRCh38.p7	15:58985880	GAAAAGGGGAGGGGA[C/G]AGGGAGAAGAGGAGG	54778
rs776903441	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59034343	GGTATATGCATTGAA[A/G]ATGTTGTTGGCTGTT	54778
rs776912339	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59086029	TTTTGTATACCAAGA[-/T]TACTCTTAATCCACT	54778
rs776927405	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59058047	CTTTTATTTCCTTTT[A/G]CTGTTTTCTTCTTTG	54778
rs776929533	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59090519	ACAGGCGCAAGCCAC[C/T]GCACCCGGCCCCCGT	54778
rs777020977	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59016083	CTCAAGCAGTCTGCC[C/T]ACCTTGGCCTCCAAG	54778
rs777026242	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59033624	ATGGTTGATGTGGAG[C/G]AGAAGTTCTAAGGAG	54778
rs777035665	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59055403	TGTAAATAGTTTATT[A/G]TAACCTGGGTAAATT	54778
rs777038339	snp	A/T	8.26918e-05	0.00642955	intron-variant	RNF111	GRCh38.p7	15:59089803	GTCACAGTATCTTTA[A/T]TGCAGATTGAGTATA	54778
rs777051746	snp	A/C	0.000314172	0.0125294	missense	RNF111	GRCh38.p7	15:59081170	ATCTTCCTCCTACAC[A/C]CCAGCCAATTTCGCA	54778
rs777066882	snp	A/G			downstream-variant-500B	RNF111	GRCh38.p7	15:59097480	ATTTGAACCATAACA[A/G]TTGTGATAAACTGAT	54778
rs777080278	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59068457	ACTAAAATACAAAAA[C/T]TAGCTGGGTGTGATG	54778
rs777080327	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59080761	ACATAAGATATCCAA[A/G]ATTATTGTAAGAAGG	54778
rs777080771	snp	G/T			upstream-variant-2KB	RNF111	GRCh38.p7	15:58987017	CCAATTTATAGAGGA[G/T]GAAACTAAGATTTAT	54778
rs777132828	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59038348	TTCCATGTGTAGTCC[A/C]TACTGTATTGACTTT	54778
rs777136834	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59053175	AGTAATTTTATCGGT[C/G]CTCTGAACTAACACA	54778
rs777141665	snp	A/G	1.65603e-05	0.00287747	missense	RNF111	GRCh38.p7	15:59066788	GGAGAACTACATCTA[A/G]TGCTGTAACGGAAAC	54778
rs777143432	snp	A/G	1.64925e-05	0.00287158	synonymous-codon	RNF111	GRCh38.p7	15:59081252	GATGCAGAGGATGGA[A/G]GTTCAAAGGAGGAGG	54778
rs777167602	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:58993371	AAAATAAAAAAAATA[A/T]AACTGTAAATACAAA	54778
rs777173756	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59010968	AGTGTCTGAAGAAGT[A/C]ATCTAATTTCCCCTT	54778
rs777178689	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59005885	ATTTTCATTTTTCAG[A/T]TGAGGAAATTCAGGC	54778
rs777200048	snp	A/G	1.6476e-05	0.00287014	missense	RNF111	GRCh38.p7	15:59031172	ACCAGGGAATATTAG[A/G]ACTGAGGCAACACCT	54778
rs777217277	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59044069	GAGTTTCGCTTTTGC[C/T]GCCCAGGCTGGAGTG	54778
rs777220874	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59027238	CCAAGATCTCCTCCT[C/G]TGAAATCCACCAGAA	54778
rs777246337	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59084383	CCCAGTTTAACTGAG[A/T]CACTGCCTCTGGGCA	54778
rs777262691	in-del	-/GACACA			intron-variant	RNF111	GRCh38.p7	15:59075160	GAATTACCAAAATGT[-/GACACA]GACACAGAGTTTCCA	54778
rs777270846	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59014109	TTTTTAAATTTTGGA[G/T]TAGAATTAATACTAC	54778
rs777277081	snp	A/G	1.75203e-05	0.00295971	missense	RNF111	GRCh38.p7	15:59030845	AATGGACTCCTGAAT[A/G]TAACGAGCTCTACAC	54778
rs777278211	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59004935	CTTGGGAAGTGAGAC[C/G]CAGTGGAGAGCAGCA	54778
rs777286992	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58994852	ATTTGTTTCTAAATA[C/T]TCACTGTGTATTGTA	54778
rs777301203	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59044331	CCACCACGCCTGGCC[A/G]TGGAAACTCTTCTTA	54778
rs777312581	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59085248	TTTGCTATTCTAATC[A/G]TCCTTAATGTCAACA	54778
rs777337712	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59056442	ATTTGCCCACATATT[A/G]GGAATCATCTTGAGG	54778
rs777347918	snp	A/G	1.6517e-05	0.00287372	splice-acceptor-variant	RNF111	GRCh38.p7	15:59091057	ATATTCTTCACTTTC[A/G]GGAACTGATTCATTT	54778
rs777357576	in-del	-/ATT			intron-variant	RNF111	GRCh38.p7	15:59060788	GCTTTATGTAGCATT[-/ATT]ATTATTATTATTATT	54778
rs777386115	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59032471	TTGTTGCTCAGGCTG[A/G]AGTATAGTGATGCAG	54778
rs777394754	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59031945	ATAACCCTTCATTAC[-/T]TTTTTTTTTCTGAAA	54778
rs777398151	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59079010	AAGTGATATGTTGAA[A/C]GTCTAGGAAACAATA	54778
rs777424007	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59057647	TGATAGAAAAATGTT[A/G]ATTTTTATTAGAAAG	54778
rs777428251	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59043090	AAATTATTGAGGTAT[A/T]ATTAACTACTATAAA	54778
rs777435853	snp	A/G	1.65081e-05	0.00287293	missense	RNF111	GRCh38.p7	15:59076203	TCATGTCGACATTAC[A/G]TGCCACCCCCTTGTA	54778
rs777477118	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59091834	GATTATCAGGCATTA[A/G]TTAGATTCTCTTAAG	54778
rs777488688	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59000337	CTTGGCTCATTTTTC[C/T]ATTTTTAGTAGAGAC	54778
rs777546844	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59015294	TAGCATGTTAGAGAT[A/G]TTGTCATGTTTTGTG	54778
rs777583732	snp	A/T	1.64754e-05	0.00287009	missense	RNF111	GRCh38.p7	15:59031256	CTCCTTCATCTAGTC[A/T]GCATTTTGGAGATTC	54778
rs777596024	snp	C/T	1.64738e-05	0.00286995	missense	RNF111	GRCh38.p7	15:59081200	ACCATATTCCAGCCA[C/T]AGCACCTCCAGCACA	54778
rs777623019	in-del	-/AG			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021885	ATTTTTTTTTGAGTC[-/AG]AGTTTGCTCTGTCAC	54778
rs777667954	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59037665	AACATGGAGAAACCC[C/T]GTCTCTACTAAAAAT	54778
rs777674055	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59025950	GGTCAGGCTGGTCTC[A/G]AACTCCCAACCTCAG	54778
rs777685333	snp	G/T	1.64917e-05	0.00287151	synonymous-codon	RNF111	GRCh38.p7	15:59085683	AATTGAAGCTGGAGT[G/T]ACTGCAGCTACTTAT	54778
rs777712592	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59077759	ACTTTCAGATAAATA[C/T]TGTTAAGTTTTCTCT	54778
rs777744167	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59009152	TTTAGTAGAGATGGG[A/G]TTTCACCAAGTTGGC	54778
rs777757480	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59047907	GTTATTAAAACCACA[A/G]TGAGATACCACGTAT	54778
rs777771378	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59059050	TGAGGGGTTGAGGGT[A/G]GAGGATCACTTGAGA	54778
rs777772451	snp	A/C	0.000115313	0.0075923	missense	RNF111	GRCh38.p7	15:59066853	TGTCCCCAGCACTCA[A/C]CATGTGGAGGGTCGT	54778
rs777773367	snp	A/G	1.71764e-05	0.00293051	intron-variant	RNF111	GRCh38.p7	15:59075916	TGAAATATTTGACCA[A/G]ACTTTAGAAAGATAA	54778
rs777795120	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59028655	ATTGGCATTTGTGTT[C/G]CCACTTTTTTGGCTG	54778
rs777802666	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59090042	TATATAACTATACCA[A/T]TAAATGTGGTGGGGA	54778
rs777811402	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:58998875	TGAAAGAGGTGCGTA[A/T]CTTGGTGAAACAATA	54778
rs777834960	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58999335	GATATAATGGGTTTG[C/T]AGTGGGGTTTGTTTG	54778
rs777842328	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59084337	TTGTGATTGATTGCT[G/T]TGCAGAAGGATGATG	54778
rs777858149	snp	A/G	1.66535e-05	0.00288556	synonymous-codon	RNF111	GRCh38.p7	15:59031680	CAGTGAAAACCACCA[A/G]AACAATCCAGCTGTT	54778
rs777860164	snp	C/T	1.64738e-05	0.00286995	missense	RNF111	GRCh38.p7	15:59066959	ACCACCACCACCATA[C/T]TCCCCACCCAGCTGT	54778
rs777870214	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59036554	TGTTCACTACCGTGA[C/G]AACATGGTATGTGGG	54778
rs777879902	snp	A/G	1.67877e-05	0.00289716	intron-variant	RNF111	GRCh38.p7	15:59067092	TGAACAGGTATGTGG[A/G]ATTTGAGTCAGTCTT	54778
rs777881520	snp	A/G	1.84681e-05	0.0030387	missense	RNF111	GRCh38.p7	15:59092553	GGAAACTGCACTGCA[A/G]ACAAGATGGGGAAGA	54778
rs777889973	snp	C/G	1.67279e-05	0.002892	intron-variant	RNF111	GRCh38.p7	15:59052436	GAAAGCTATCGGTGA[C/G]ATTTTAATTCTTAGT	54778
rs777960641	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59074177	CACAGGCAGAATAGA[A/T]TTAGCATAAATCTTA	54778
rs777978099	snp	C/T	1.64735e-05	0.00286993	synonymous-codon	RNF111	GRCh38.p7	15:59058435	CAATTCAAATCCATC[C/T]ACCTCTGAGCAGGCC	54778
rs777979603	snp	A/G	3.72405e-05	0.00431496	missense	RNF111	GRCh38.p7	15:59055687	GTCATTTAAGGTCTC[A/G]TTCAACCCTTGGACA	54778
rs777985683	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59027992	CACCATGCCCGGATA[A/C]TTTTTTGTATTTTTA	54778
rs778059671	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59091783	CATGGATAGGTGGCA[C/G]AGGGGATAGTTTCAG	54778
rs778070809	in-del	-/AG	1.6495e-05	0.0028718	frameshift-variant	RNF111	GRCh38.p7	15:59031389	GCCTCGGACTGAGAC[-/AG]AATCTGTATCGGGAT	54778
rs778133937	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59033061	GCATTGAAGAGCTGT[C/G]TGAACTGAGGGAAAA	54778
rs778235046	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59010763	CCCTGCTTGAAGGTA[A/G]TGGAAAAGTTGAGAC	54778
rs778248745	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59052054	TAGAAACCACTGAAC[A/G]TCTGTAATGAATACA	54778
rs778253298	in-del	-/CAGCCC	0.000181334	0.0095202	cds-indel	RNF111	GRCh38.p7	15:59076148	TCAAGCATGGTTGCG[-/CAGCCC]CAGCCCCAGCCCCAG	54778
rs778271361	snp	C/T	1.64969e-05	0.00287196	synonymous-codon	RNF111	GRCh38.p7	15:59058540	TAGTACCACTGGCAC[C/T]TCTATAGGAGGTATG	54778
rs778353336	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59085958	TAAAATCTGCACGTA[-/T]AATTTGCATCATAAC	54778
rs778357414	snp	A/G	1.65198e-05	0.00287395	missense	RNF111	GRCh38.p7	15:59031463	GACTTCCATGCAGAA[A/G]GAGATTTGTAAAAAA	54778
rs778365836	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59062807	TACTTTTCCCCTTTA[C/T]GCCAAGATTTCTCAA	54778
rs778367333	snp	A/G	1.66255e-05	0.00288314	synonymous-codon	RNF111	GRCh38.p7	15:59084240	TCCTCGACAGGCTCC[A/G]GAGAGGTCTGCCTGG	54778
rs778417951	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59024270	AGAAATATGGCAGTT[A/G]TGTTTTACTTCCTTC	54778
rs778438555	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59013155	TTTCCTAGGGATCAG[C/G]GGAAGTTTGTAAATA	54778
rs778438999	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59013972	TTTTGTATTTTTTAG[G/T]GGAGACAAAGGTTTC	54778
rs778443927	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59056188	TTTTAAATATAAACA[A/C]AAAAGCAGTATAACT	54778
rs778451240	snp	A/G	1.6486e-05	0.00287102	intron-variant	RNF111	GRCh38.p7	15:59092490	TTACTCAGTTGTTCA[A/G]TAATGTCATCTCTAC	54778
rs778455748	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59063727	CGAAGGCAAAAGAGG[A/G]CAAGCTGTTTCTGAA	54778
rs778456265	snp	G/T	1.6473e-05	0.00286988	missense	RNF111	GRCh38.p7	15:59058448	TCTACCTCTGAGCAG[G/T]CCTCTGATACTGCTT	54778
rs778516079	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59008006	GAGGTTTTGATTTTG[A/G]TAAAGTCAAGCTTAC	54778
rs778535009	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59042098	AAATTAATTAGTAGT[C/T]TCTTGACTTACATAC	54778
rs778545040	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59089094	TGCAATTTTTTGCCA[A/C]CGGTCATATCCACGA	54778
rs778635908	snp	G/T			missense, intron-variant	RNF111	GRCh38.p7	15:59084103	TCAATTATTTCCAGT[G/T]GTCTTTTTGTGTTCT	54778
rs778636573	snp	C/T	1.64991e-05	0.00287215	synonymous-codon	RNF111	GRCh38.p7	15:59067056	TTGTGGAGCAAATAG[C/T]AGTTCTGGTACCAGC	54778
rs778652545	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59076344	TTAAGAGTAGGGTAT[A/G]TTTTTTCCCATGTTA	54778
rs778680184	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:58998244	TGACAAAATGGGAAG[-/T]TTTTTTTTTTTTTTT	54778
rs778728693	snp	A/C	1.65597e-05	0.00287743			GRCh38.p7	15:59052423	TGTAACAGTTGGAGA[A/C]AGCTATCGGTGAGAT	54778
rs778734872	snp	A/G	1.65002e-05	0.00287225			GRCh38.p7	15:59091096	GATTAGGCAATGTCA[A/G]TCGTGGAGCATCCCA	54778
rs778746322	snp	A/G					GRCh38.p7	15:58988737	AGTTTTGATTATTCA[A/G]AAAATACCAGAAAGT	54778
rs778761147	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59081509	CTTTTTTTAAAAAAA[A/G]AACAAAGAACAGCAA	54778
rs778789989	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59001609	TCTCCACATTTGGCG[A/T]ATAGGTTCACTTTAG	54778
rs778800060	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59017842	GGCTCTCTGCAACCT[C/T]CACTTCCTGGGTTCA	54778
rs778828930	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59080402	GCTGGGATTACAGGT[A/G]TGAGCCACGGTGCCT	54778
rs778833389	snp	A/G	1.67354e-05	0.00289265	intron-variant	RNF111	GRCh38.p7	15:59052267	AACGATTAGCTGACA[A/G]GAAGATGCCTTTAAA	54778
rs778839209	snp	G/T	8.23906e-05	0.00641783	missense	RNF111	GRCh38.p7	15:59076016	AAGTGGCAGTTTTCA[G/T]GGAGCATCTGCATTT	54778
rs778843647	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59059950	TAATATTCATGTAAT[C/T]TACATCTAGCAGATT	54778
rs778880123	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58990723	TGTCCCATTGTAGAT[A/G]TTAATTACTGAAGCT	54778
rs778889005	snp	A/G			utr-variant-3-prime	RNF111	GRCh38.p7	15:59095704	TAAATATTAATTTCA[A/G]TTAGCTAGATTGTAC	54778
rs778889975	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59019194	TCCACCTGCCTTGGC[C/T]TCACAAAGTGCTGGG	54778
rs778929008	snp	A/G	1.66466e-05	0.00288496	missense	RNF111	GRCh38.p7	15:59055762	GGCCACAGGAGCCAC[A/G]GAACCGCAGTAGGAT	54778
rs778935093	snp	A/G	0.000215866	0.0103868	intron-variant	RNF111	GRCh38.p7	15:59093481	CTCCCAAAATGCTGG[A/G]ATTACAGGCGTAAGC	54778
rs778982678	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58994723	CTTTAAGTGATCAGC[C/T]TACTTCAGCCTCCCA	54778
rs779004379	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59038988	TTATTTTTTGAGATG[A/G]AGTTTCACTTTTGTT	54778
rs779005978	snp	A/T	6.31692e-05	0.00561966	intron-variant	RNF111	GRCh38.p7	15:59030785	AAAAATCTTTTAAAT[A/T]TCTAATTTTGTCTTC	54778
rs779010153	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59054395	TACAATATGATGCTT[G/T]CACAAAAGTACTGCA	54778
rs779015775	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59047088	TCAGCCTCCCAAAAT[A/G]CTGGGATTACAGGCA	54778
rs779029616	snp	G/T	1.75829e-05	0.00296498	synonymous-codon	RNF111	GRCh38.p7	15:59055697	GTCTCGTTCAACCCT[G/T]GGACACTCCAGATCT	54778
rs779092875	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59040119	TTGAATTTAACCTAA[-/T]TTTTTTTTTTTTAAA	54778
rs779120974	snp	A/G	3.29527e-05	0.00405898	missense	RNF111	GRCh38.p7	15:59031139	GCCCTTCGTATGTGC[A/G]GAATTGTGTTAAAGA	54778
rs779214952	snp	C/G/T	3.29648e-05	0.00405974	intron-variant	RNF111	GRCh38.p7	15:59094773	CTTTTTGTTTTCTTG[C/G/T]CAATAATAGACGTCT	54778
rs779245057	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59017508	TATATTTATAAAAAC[A/G]TCAATTGTCTTTAGG	54778
rs779259302	snp	C/T			intron-variant, utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022253	TTAGCTAGTTCTCTA[C/T]CCTAAGTGTTTTGAG	54778
rs779288660	snp	C/T	3.29804e-05	0.00406068	synonymous-codon	RNF111	GRCh38.p7	15:59031563	AGCTCGAAGAAAATA[C/T]GCCTTGCTACCTAGT	54778
rs779296708	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59032905	CTCTCTCTCTCTCTC[A/T]CACACACACAGTAAA	54778
rs779348889	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59010559	GGTGCCCACCACCAC[A/T]CCTAACTAATTTTTA	54778
rs779364322	snp	A/G			intron-variant, utr-variant-5-prime	RNF111	GRCh38.p7	15:59004009	CATTCCAGATGCTTG[A/G]GATGGAAGAAGTTTG	54778
rs779366540	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59003816	TCGTGGCTGATGCCA[G/T]TGCCTAAAACAAGTG	54778
rs779367614	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59040039	TTTATTGGGAGGTGA[C/T]AGAGACTACAGTCTG	54778
rs779383963	snp	C/T			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021193	TCTTGCTCTGTTGCC[C/T]AGGATGGAGTGCAGT	54778
rs779387698	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59026149	TGAAGCATCATACCA[A/G]TAATAGTGTATCACA	54778
rs779455764	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59004892	TAGAATCTGACAGCA[C/T]AGTAAGATGCTCACA	54778
rs779461908	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58993681	TTTCAGGCACTGTGC[C/T]AGTGCTTGAGTTAAA	54778
rs779479891	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59066601	GCAACAACAGCAAGA[C/G]TCCATCTCAAAAAAA	54778
rs779507691	snp	C/T	3.29777e-05	0.00406051	missense	RNF111	GRCh38.p7	15:59085703	CAGCTACTTATACAC[C/T]TGGTGCATTGCATCC	54778
rs779507793	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59085222	CCCTTCTTTTATAAG[A/G]TGTAGAAGAGTTTGC	54778
rs779555187	snp	C/T			upstream-variant-2KB	RNF111	GRCh38.p7	15:58987263	GGAAGCAAATTCACT[C/T]TAACAGTGAGGTGCC	54778
rs779559607	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59034190	CATTTGCATAGTATT[C/G]CCTTTGTATGGATGT	54778
rs779592066	snp	C/T	1.64746e-05	0.00287002	stop-gained	RNF111	GRCh38.p7	15:59081070	CATGCTTTCCATTCT[C/T]AAATATCTTCTCATG	54778
rs779599277	snp	C/G	1.65282e-05	0.00287469	missense	RNF111	GRCh38.p7	15:59085762	CGACTTCATCACTTA[C/G]AATTAGGAGCTCTTC	54778
rs779643210	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58989441	TCTAAGAATTGGTGA[A/G]GGTGTTTATAAATCT	54778
rs779667818	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59053657	CAGTGTTATGTACCA[C/T]ACCTATCCTCTGACC	54778
rs779668537	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59017368	ACAAAAAAATTAATA[G/T]TTCAGTATGTAAAAT	54778
rs779682156	snp	A/T	1.66866e-05	0.00288842	intron-variant	RNF111	GRCh38.p7	15:59058598	TGTCATTACTTTCGT[A/T]AGGAAAAGTATTATT	54778
rs779685201	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59023177	CGGTTGAATCCGGGA[A/G]GCGTAGGTTGCAGTG	54778
rs779691326	snp	C/G	1.64993e-05	0.00287218	missense	RNF111	GRCh38.p7	15:59031580	CCTTGCTACCTAGTT[C/G]TAGTAGTTCCAGTGA	54778
rs779743766	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59046567	ACCTGTTGTCTGACA[C/T]AGAAATTAACAAAGT	54778
rs779750501	snp	A/C	2.91813e-05	0.00381966	intron-variant	RNF111	GRCh38.p7	15:59055658	TTATTTATATTTACT[A/C]ACTTAATATTGATGT	54778
rs779751859	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59048402	AAATCCAAACCAATT[C/T]ATAATGACAGAGAGC	54778
rs779754560	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59045624	GCCCAGTTTATGGGT[A/T]GAAATAAGGAAAGTT	54778
rs779760094	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59035002	TTGGCTCACAGTTCC[A/C]CATGGCTGGGGAGGC	54778
rs779774340	snp	C/G	1.64866e-05	0.00287106	missense	RNF111	GRCh38.p7	15:59085722	TGCATTGCATCCTCA[C/G]TTGGCCCATTATCAC	54778
rs779803796	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59086514	GACAAGTTCAGCAAA[A/G]CATACATTGCGTTTG	54778
rs779822029	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59062665	TGCCTATAATAACTC[-/T]TGATTTTTACAGTAA	54778
rs779827011	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:58995992	TAAATTTAAATTAGA[A/T]TTTTGATAGTAGGTT	54778
rs779838355	snp	A/C	0.000164867	0.00907779	missense	RNF111	GRCh38.p7	15:59031014	AGTGGGGAATGAATT[A/C]TCTCACCTGTGTGAT	54778
rs779847668	snp	C/T	3.32995e-05	0.00408027	missense	RNF111	GRCh38.p7	15:59052430	GTTGGAGAAAGCTAT[C/T]GGTGAGATTTTAATT	54778
rs779848133	in-del	-/ATTA			intron-variant	RNF111	GRCh38.p7	15:59056793	GTTAATGTAATAGGG[-/ATTA]ATTAATTAATGATTA	54778
rs779884983	snp	A/G	1.68653e-05	0.00290385	missense	RNF111	GRCh38.p7	15:59080960	TGACAAGGCCACTTC[A/G]TCATCAAGCTTCTGC	54778
rs779893709	snp	C/G/T			intron-variant	RNF111	GRCh38.p7	15:59074826	TTTTGACATGCCTTC[C/G/T]TCACTAAGCTTAATC	54778
rs779915663	in-del	-/TAA			intron-variant	RNF111	GRCh38.p7	15:59012332	CCTGCTGTTCTGTCT[-/TAA]TTTCCACTTAGGTAA	54778
rs779916739	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58997953	TCCGTTGCCCAGGCT[A/G]GAGTGCAGTGGGGCG	54778
rs779935654	snp	C/T	6.77713e-05	0.00582075	missense	RNF111	GRCh38.p7	15:59030853	CCTGAATATAACGAG[C/T]TCTACACCTTAAAAG	54778
rs779948756	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59090256	GTTTTTTTAGATGGA[C/G]TCTTGCTCTGTCACC	54778
rs780007478	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59009376	CTCTGTGAGGGAAGA[C/T]GCTAGTAGAACCCAC	54778
rs780009409	snp	A/G			downstream-variant-500B	RNF111	GRCh38.p7	15:59097749	CTGGTCATGGGTAGC[A/G]GGTGCCTGTAGTCCC	54778
rs780034555	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59036660	AGATTTGGGTGGGGA[C/G]AAAGCCAAACCATAT	54778
rs780048030	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59016973	AATGCCTGATGATCT[A/G]TCACTGTCTCCCATC	54778
rs780072407	snp	A/T			utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096164	AAAGTTAAGTTAACA[A/T]ACTAACATTTCTCCT	54778
rs780084987	snp	C/T	2.03205e-05	0.00318745	intron-variant, missense	RNF111	GRCh38.p7	15:59092531	ACAACTGATTGGTTC[C/T]CACAGAGGAAACTGC	54778
rs780099637	snp	C/T	1.64792e-05	0.00287042	missense	RNF111	GRCh38.p7	15:59094784	CTTGCCAATAATAGA[C/T]GTCTTCCATGTATGC	54778
rs780131089	snp	A/T	1.64749e-05	0.00287005	missense	RNF111	GRCh38.p7	15:59031156	AATTGTGTTAAAGAA[A/T]ACCAGGGAATATTAG	54778
rs780134458	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59000433	GAAGGACCTCAGGAC[C/T]GGGCCTGGTGGCTCA	54778
rs780137430	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59080440	CCTGTGTACTCTTGA[A/T]GGAAATATTAATTAT	54778
rs780150857	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59049204	CCTCGCTCTGACCCT[G/T]GTTACCACCACTCTT	54778
rs780162725	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59058666	GGTATTCTTACATTA[A/T]AATAAACTTCATATG	54778
rs780164039	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:58995764	TGCCGTGCCCCGGCC[-/T]TTTTTTTTTTTTTTT	54778
rs780174732	snp	C/T	0.25052	0.249999	intron-variant	RNF111	GRCh38.p7	15:59093362	TTTTTTTTTTTTTTT[C/T]CTTTTCTGGGAGATG	54778
rs780187629	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59061360	CCTCACATTCAAGCC[A/G]TCTAGCTTCACACTT	54778
rs780195312	snp	C/T	1.64749e-05	0.00287005	utr-variant-3-prime	RNF111	GRCh38.p7	15:59094941	CCCTCTCATTCCCAT[C/T]CTTCCTGGTACTGCA	54778
rs780195378	snp	C/T	4.94352e-05	0.00497143	missense	RNF111	GRCh38.p7	15:59081226	GCACAGAGACTGCAT[C/T]CTCATGAAGTGATGC	54778
rs780204179	snp	C/G			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021072	CCCTGACCTCACTTT[C/G]CACCCTTTCCCCCAA	54778
rs780240008	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59054745	TTTTCAGCCCACTTT[A/G]ACCTTTGGAGTTCTC	54778
rs780247073	snp	A/C	1.68337e-05	0.00290114	missense	RNF111	GRCh38.p7	15:59085782	AGGAGCTCTTCCTTT[A/C]ATGGTAAAATGGAAA	54778
rs780280758	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59062607	CCCTCTAGTGGATAG[C/T]AATAGCTAACATTTA	54778
rs780346621	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59079259	AAAACTTTGCAACTA[G/T]AAAAAATGCTGTGAA	54778
rs780354294	snp	A/G	3.32336e-05	0.00407624	missense	RNF111	GRCh38.p7	15:59031663	GATTTGTTTGTTTCT[A/G]CCAGTGAAAACCACC	54778
rs780381520	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59089279	CAAAAAAGGCATAGG[G/T]TACTTTGGCTGTTAG	54778
rs780399653	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59031902	AAAAATTTCTAGTGA[C/G]AAAAATAAGTCAGAG	54778
rs780405646	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:58995262	GTTTATTTTGTAACT[C/G]ATCCATTTTCTTCAC	54778
rs780435564	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59083810	TTTTATTTTTATTTA[A/T]TTCCTATTATTCTCC	54778
rs780485366	in-del	-/ATTTA			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986962	TATATAAATTGTCTC[-/ATTTA]ATCTAACAAGAACCT	54778
rs780526325	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59030272	AATTAATAGAGTAGT[A/G]TGAAGGAAAAAAAAT	54778
rs780550692	in-del	-/TAAT			intron-variant	RNF111	GRCh38.p7	15:59030418	GTAAAACATGTTGAC[-/TAAT]TAGTCTTTTGAATTC	54778
rs780552366	in-del	-/CT			downstream-variant-500B	RNF111	GRCh38.p7	15:59097632	GCCTGTAATCCCAGC[-/CT]ACTTTGGGAGGCTGA	54778
rs780602616	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:58997625	AGATCGAGACCATCC[C/T]GGGCAACATGGGGAA	54778
rs780618605	snp	A/C	1.64787e-05	0.00287038	missense	RNF111	GRCh38.p7	15:59076035	GCATCTGCATTTGAC[A/C]CCTGCTGCCCTGTTT	54778
rs780638284	snp	A/G			intron-variant, missense	RNF111	GRCh38.p7	15:59022535	TATCCAGACCAACAT[A/G]GAATGGAGGATGTCC	54778
rs780638332	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59034025	AAAATAAAAGTTTAT[C/T]TCTTCTTCAGATCCT	54778
rs780683893	snp	A/C			utr-variant-3-prime	RNF111	GRCh38.p7	15:59095301	TTATCCATTACTAAC[A/C]TTTAATTTAATCAAT	54778
rs780700200	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59041018	ATACCCAAAATATGA[A/C]CCCCTTCTCTTACTC	54778
rs780704155	in-del	-/TATTT			intron-variant	RNF111	GRCh38.p7	15:59008954	TATTGTCACGTATTT[-/TATTT]TATTTTATTTTATTT	54778
rs780707062	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59044402	GGTGATCAGTGAGTA[C/T]AGTGGCTAACGTTGC	54778
rs780718515	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59041797	CAGAATATGTTGTCA[C/G]ATTTTAGGGGGTTTT	54778
rs780719823	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59074548	GACTTTTCTTCTGCA[A/G]CCTCCTTGCCTCCCT	54778
rs780824042	snp	C/G	1.66535e-05	0.00288556	missense	RNF111	GRCh38.p7	15:59031677	TGCCAGTGAAAACCA[C/G]CAAAACAATCCAGCT	54778
rs780828924	snp	C/T	1.64806e-05	0.00287054	missense	RNF111	GRCh38.p7	15:59066820	GGCCCTCCTGCAATG[C/T]CAAGGTTACCTTCCT	54778
rs780838149	snp	G/T	1.74531e-05	0.00295402	intron-variant	RNF111	GRCh38.p7	15:59085800	GGTAAAATGGAAAAT[G/T]TTCAAAATTTTGACA	54778
rs780845051	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59089376	TTTTTTGTTGTTGTT[C/T]TAATAAAGCTCTCTG	54778
rs780848272	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59086200	TCTCAGCTCACTGCA[A/G]CCTCCACCTCCTGGG	54778
rs780901101	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59057726	AAAGGCATGGAAAGG[A/C]GATTAAAACAGTTAT	54778
rs780913928	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59045493	TGCGCCCGGCCTTAG[C/T]TTTTCCTCTTTTTAA	54778
rs780916422	snp	C/G	1.66496e-05	0.00288522	missense	RNF111	GRCh38.p7	15:59055754	TGCAAGTCGGCCACA[C/G]GAGCCACGGAACCGC	54778
rs780926264	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59064049	TGAGTAATTACTATA[C/G]ATATTATAATTTATA	54778
rs780958004	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59005015	AGAAGGGCAAGCATA[A/G]TCTCCTACATGGTTT	54778
rs780960677	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59003998	GGTTTTGTTCTCATT[C/T]CAGATGCTTGGGATG	54778
rs780997091	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59073867	TTCTTTAATAGTAAG[A/G]CTTGAAAGTTGAAAT	54778
rs781034748	snp	C/G			downstream-variant-500B	RNF111	GRCh38.p7	15:59097648	ACTTTGGGAGGCTGA[C/G]GTGGGCAGATCATGA	54778
rs781045596	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59005965	GGAGATTTAAATCAA[A/T]GCATTTTGAGTTGCC	54778
rs781082606	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59024314	TTTTACAGATTAATG[C/T]AATTAAAAAAAATAC	54778
rs781088183	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:58989547	TCTGTCACTTCTTAA[C/G]TTTTGTTTGGTGTCT	54778
rs781151249	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:58990269	CTAGTTAGGTTTTTG[A/G]TATTCATTGTTGTGT	54778
rs781168506	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59001440	GTTGATTAAAAAAAA[A/C]TTCTTTTTACTATCA	54778
rs781173720	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59037808	GCCATTGCACTCCAG[C/G]CTGGGCAACAAGAGT	54778
rs781175509	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59047135	GCCAGGAATTCTTAT[A/G]ATTCAACAATGAGAC	54778
rs781191058	snp	C/T	1.64735e-05	0.00286993	missense	RNF111	GRCh38.p7	15:59081104	CATCTCATCCTGTGG[C/T]ACCCCCACCACCAAC	54778
rs781215536	snp	G/T	0.000106425	0.00729393	intron-variant	RNF111	GRCh38.p7	15:59084073	TCTACATTAAGAAAA[G/T]AAATAACCAATTATT	54778
rs781256835	in-del	-/A			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021287	TGGCCAGTAGCTGGG[-/A]TTACAGGTGGGTGCC	54778
rs781277317	snp	A/G	1.77972e-05	0.002983	intron-variant	RNF111	GRCh38.p7	15:59066721	TTTTTACACAGTGAT[A/G]TTTCATGATTTGATT	54778
rs781278987	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59048673	TATTGACAGGTGATA[A/G]TAATGAAGAAGCCAT	54778
rs781285662	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59035588	TATCACATTGTCAGG[C/G]TGCAAATTTTGCAAA	54778
rs781296552	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59060110	AGTTCCAGGCTCAGG[C/T]GATCCTCCTACCTCA	54778
rs781306163	snp	A/G	1.65168e-05	0.00287369	missense	RNF111	GRCh38.p7	15:59084214	CATGTGCCTCAGACT[A/G]TGTCCTCACATCCTC	54778
rs781309526	snp	C/G	1.64749e-05	0.00287005	missense	RNF111	GRCh38.p7	15:59081196	TCGCACCATATTCCA[C/G]CCACAGCACCTCCAG	54778
rs781311447	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59068712	TTTCTATGTCACCCG[A/C]CCTTTCCTAAAGTAC	54778
rs781351296	in-del	-/TC/TCTC	0.0251412	0.109267	intron-variant	RNF111	GRCh38.p7	15:59067125	TTCCTGCCCCTCTTG[-/TC/TCTC]TCTCTCTCTCTCTCT	54778
rs781351756	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59002467	AAATACGGGAAGTAC[A/G]GTTGAGTAACATATG	54778
rs781423620	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:59089212	ATGAAGATTGACTGT[A/C]ACTAACAAAAAATTA	54778
rs781437442	in-del	-/GTTTTG			upstream-variant-2KB	RNF111	GRCh38.p7	15:58986205	TGTGTGTGTGTGTGT[-/GTTTTG]TTTGTTTGTTTGTTT	54778
rs781459240	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59028824	TTGCTCTGTTGCTCA[A/T]GCTGGACTGTAGCGG	54778
rs781473598	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59034181	TCTTCTTGACATTTG[C/G]ATAGTATTCCCTTTG	54778
rs781512668	in-del	-/CTGGCCCTTCGT	1.64779e-05	0.00287031	cds-indel	RNF111	GRCh38.p7	15:59031121	GCAAAAGCCAGCAGG[-/CTGGCCCTTCGT]ATGTGCAGAATTGTG	54778
rs781548384	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59041630	TTTGTTTGACAGTGT[A/G]TCTTTGGAATAGTAT	54778
rs781558992	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59012928	ATTTTTAGTTGAGAC[A/G]GGGTTTCGCCATGTT	54778
rs781598745	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59070407	CTTAATCACTGACTA[C/G]AGATGAAGATAAAAT	54778
rs781602409	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59082768	AAACTCTTGATCTAA[A/T]TAATGATCCAGCTCT	54778
rs781641499	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59003180	GAGTGCAGTGGCTCA[A/G]TGTCAGCTCACTGCA	54778
rs781644881	in-del	-/TAT			intron-variant	RNF111	GRCh38.p7	15:59046095	AGAATATAAATACAA[-/TAT]TATTAAGTAATTTTT	54778
rs781645269	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59023102	AAATACAAAAAATTA[A/G]CTGGGCATGGTGGTG	54778
rs781713906	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59023792	AACCATCAGTTTTTT[G/T]CCCCCTGAATTATGT	54778
rs781731247	snp	A/G	2.01635e-05	0.00317512	intron-variant	RNF111	GRCh38.p7	15:59055896	GGAGTTTGATAAAAG[A/G]AAATCTCTTAATATG	54778
rs781734637	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59052484	AAATATAAATATTAA[A/G]CATATTTGTGCTGCA	54778
rs781752655	snp	C/T			intron-variant, utr-variant-5-prime, upstream-variant-2KB	RNF111	GRCh38.p7	15:59022232	TCCTCTTAGTGGTTT[C/T]GTCTGTTAGCTAGTT	54778
rs781771143	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59053479	TTAAAAGTATATATT[C/T]ATATTTCTGACATCT	54778
rs796069158	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59072599	GGGACTACAGGTGCC[C/T]GCCACCACGCCTGGC	54778
rs796107677	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59062097	GGTCTTGCTTTGTCA[C/T]GTAGGCTAGAGTGCA	54778
rs796122264	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59093168	ATATACTGCCTATTG[C/T]AGGGCCACACAAGGT	54778
rs796266834	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59026035	GTGCCCGGCCGGCTT[G/T]TTTTTTTTCTTTTAA	54778
rs796269857	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59035714	CTCTAAGGCAGAGGC[-/A]AAATGCTGCCAGTCT	54778
rs796299971	in-del	-/TT			intron-variant	RNF111	GRCh38.p7	15:59027837	TGCACCTGGCCCACC[-/TT]TTTTTTTTTTTTTCC	54778
rs796327954	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59006726	ACAGACGCCAGTGCA[C/T]TTTACCCGTAAAAAA	54778
rs796412579	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59019402	TAATGTTTATGTTTT[A/G]TAGTTTTAAAAAAAA	54778
rs796427136	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59030437	TAGTCTTTTGAATTC[A/G]AATCCTTTTATTTAT	54778
rs796432480	in-del	-/CTT			intron-variant	RNF111	GRCh38.p7	15:59054641	AACTTTATACTCCTT[-/CTT]AAGAATTTTATTTTA	54778
rs796511698	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59070357	TTAATTTTACCCTCA[G/T]TTTCTTCTAGGAATT	54778
rs796529435	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59072135	CAGCAAATTGTAAAC[C/T]TTTTGCTGATGGAGG	54778
rs796568671	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59071298	AGCGAGACTCCATCT[C/T]AAAAAAAAAAAAAAA	54778
rs796597118	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59005666	CTAGAGGATTGAAGT[C/T]GTACCAAAAAAAAAA	54778
rs796599310	in-del	AA/TTAACTCC			intron-variant	RNF111	GRCh38.p7	15:59067253	TCCTTTTTTTTTTTT[AA/TTAACTCC]TCCCATTCTTCCTTC	54778
rs796681383	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59040965	CTCAGGTCTTAATTT[A/T]GTTTTGGTTAACTCT	54778
rs796693683	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59079670	CTTTTTTTTTTTTTT[-/T]ACATGTCAAGTAGAT	54778
rs796699621	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59071317	AAAAAAAAAAAAAAA[-/A]GAATACGAAGAAGTG	54778
rs796739813	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59014648	TCTGTTTTATTCTGA[A/G]TCTAAGAAAAAATGA	54778
rs796781161	snp	G/T			intron-variant	RNF111	GRCh38.p7	15:59049818	AATGGCGCGATCTCG[G/T]CTCACTGCAACCTTT	54778
rs796781673	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59093646	CATTTTCTTTGTATA[A/G]TCACTTAAGTAATTG	54778
rs796782333	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59024296	CCTTCCTTTTACTCA[C/T]TCTTTTACAGATTAA	54778
rs796816598	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59007268	ACAACCAATGTTCAA[-/T]TTTTTTTTTTTTTTT	54778
rs796830896	snp	A/C			intron-variant	RNF111	GRCh38.p7	15:58993615	AAAAATACAGTATTT[A/C]GTTTCTATTTGTAAA	54778
rs796833495	in-del	-/AAAG			intron-variant	RNF111	GRCh38.p7	15:59011838	AATTTTGGGGAACAC[-/AAAG]AAGTTCATAGCACAT	54778
rs796855904	snp	C/G			intron-variant	RNF111	GRCh38.p7	15:59050006	CAGACTCCCAAAGTG[C/G]TGGGATTACAGGCGT	54778
rs796888402	in-del	-/G			intron-variant	RNF111	GRCh38.p7	15:59085445	AAGTAGAAATGCTTT[-/G]CTCCTCATTGTCACA	54778
rs796896236	in-del	-/TTG			intron-variant	RNF111	GRCh38.p7	15:59090230	TGTTTGTTTGTTTGT[-/TTG]TTGTTGTTGTTTTTT	54778
rs796904119	in-del	-/T			intron-variant	RNF111	GRCh38.p7	15:59000150	CAGATCTTCCAGTGA[-/T]TTTTTTTTTTCCCTT	54778
rs796917882	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59059933	ATCTCATTTAATTCT[A/T]TTAATATTCATGTAA	54778
rs796943155	snp	A/T			intron-variant	RNF111	GRCh38.p7	15:59073491	ATCTCCAAAAAAAAA[A/T]AAAATAAATAAACTA	54778
rs796950655	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59072541	TCACTGAAAGCTCCA[C/T]CTCCCAGGTTCATGC	54778
rs796952473	in-del	-/A			intron-variant	RNF111	GRCh38.p7	15:59078880	AGAAAAAAAAAAAAA[-/A]AAGAGAGGTATAGGT	54778
rs796986757	snp	A/G			intron-variant, upstream-variant-2KB	RNF111	GRCh38.p7	15:59021244	CAAACTCCGCCTCGT[A/G]AGTTCAAGTGATTCT	54778
rs796990593	multinucleotide-polymorphism	CCT/GCA			intron-variant	RNF111	GRCh38.p7	15:59061947	GTGTTCTCATCCCCC[CCT/GCA]TCACTAGCCCATTTC	54778
rs796999222	snp	C/T			intron-variant	RNF111	GRCh38.p7	15:59050154	ACTGCAATCTCCGCC[C/T]CCTGAGTTCCAGCGA	54778
rs797016714	in-del	AA/G			intron-variant	RNF111	GRCh38.p7	15:59078880	GAAAAAAAAAAAAAA[AA/G]GAGAGGTATAGGTAA	54778

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