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

RNF126

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs14218	snp	A/G/T	0.00310999	0.0393106	synonymous-codon	RNF126	GRCh38.p7	19:648224	ACAGAACACGGCCAC[A/G/T]AACCCCCCTGGCCTC	55658
rs757331	snp	A/G	0.409212	0.192748	downstream-variant-500B	RNF126	GRCh38.p7	19:647251	GGCTGAGGTGTGACC[A/G]AAGCGTGGGGCAGAG	55658
rs916904	snp	A/G	0.490727	0.0674567	upstream-variant-2KB	RNF126	GRCh38.p7	19:663929	TCTCGGGTGCGGAGA[A/G]GGCAGGAAACCTAAC	55658
rs929263	snp	C/T	0.243919	0.249926	upstream-variant-2KB	RNF126	GRCh38.p7	19:663373	GGGCGGGGCTTCCGG[C/T]GGGGGCGGGGCCAAA	55658
rs1009628	snp	A/G	0.189576	0.242588	intron-variant	RNF126	GRCh38.p7	19:658013	ACCTTCTCCGGGGGC[A/G]GCACGCACTGGGGGC	55658
rs1009629	snp	C/T	0.317692	0.240661	intron-variant	RNF126	GRCh38.p7	19:660913	AGGCACAAGCAGATG[C/T]CCTTGGGATCACCCG	55658
rs1859224	snp	A/G	0.490943	0.0666801	upstream-variant-2KB	RNF126	GRCh38.p7	19:663485	TTCGTGTCCCTCAGT[A/G]CTTCCCTACCTCATC	55658
rs2040736	snp	C/G	0.178785	0.239642	intron-variant	RNF126	GRCh38.p7	19:649110	CCTTGGAGCCCGCCC[C/G]GGGTCGGAGATCACT	55658
rs2040737	snp	A/G	0.114036	0.209795	intron-variant	RNF126	GRCh38.p7	19:649139	CTGTGGAGCCCACGC[A/G]GCCCCCCCGCTCCTG	55658
rs2040738	snp	A/G	0.238171	0.24972	intron-variant	RNF126	GRCh38.p7	19:650931	atggggcctccctac[A/G]ttgctcaggctggtc	55658
rs2040739	snp	A/G	0.190371	0.242785	intron-variant	RNF126	GRCh38.p7	19:658368	TGACTGACAGTGACC[A/G]GGGCAGGCAGGCCCC	55658
rs2072104	snp	C/G	0.100773	0.200577	synonymous-codon	RNF126	GRCh38.p7	19:648173	GGGCGAGCTGGAGGA[C/G]GACGATGACGACGAG	55658
rs2074460	snp	C/T	0.187685	0.242109	downstream-variant-500B	RNF126	GRCh38.p7	19:647039	CTCCTCTCCGTTAGC[C/T]GTCTCCATCGTCTGA	55658
rs2285751	snp	C/T	0.114459	0.210068	missense	RNF126	GRCh38.p7	19:651852	ACAGGTGCTGGTCCA[C/T]GTGCTGGGGAGAGGA	55658
rs2285752	snp	C/T	0.000654046	0.0180719	intron-variant	RNF126	GRCh38.p7	19:651874	GGGAGAGGAGGGGGG[C/T]GTGACCTCGGGGGCT	55658
rs3077449	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:655014	CCTGGGCTTTTTTTT[C/T]TTTCTTTCTTTCTTT	55658
rs3170527	snp	C/T	0.0663309	0.169604	utr-variant-3-prime	RNF126	GRCh38.p7	19:648014	TTGGCTGGTCAGCGC[C/T]GCAGGTCCCGCCTGT	55658
rs3179858	snp	A/G			utr-variant-3-prime	RNF126	GRCh38.p7	19:647530	TACACTACTTACAAA[A/G]AGAAGCCGGTGCTGT	55658
rs3180572	snp	A/G			utr-variant-3-prime	RNF126	GRCh38.p7	19:647528	CACTACTTACAAAGA[A/G]AAGCCGGTGCTGTGG	55658
rs3787004	snp	C/T	0.377582	0.214995	intron-variant	RNF126	GRCh38.p7	19:657666	CTCATATCTGAAATC[C/T]GGGTGCCATCGAGGA	55658
rs3787005	snp	A/G	0.367503	0.220665	intron-variant	RNF126	GRCh38.p7	19:658983	CAGCCGGCCAGAGAG[A/G]GCAGCCGACATCCAC	55658
rs3787006	snp	A/C	0.0170251	0.090679	intron-variant	RNF126	GRCh38.p7	19:659328	CTGGCCGTAGCAGCC[A/C]TCACTTCCTGGTGGC	55658
rs3787007	snp	A/G	0.0640965	0.167152	intron-variant	RNF126	GRCh38.p7	19:660657	CGTTTTTGAGACAGC[A/G]TCTTGCTTGTCACCC	55658
rs3787008	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:660872	TGCCATGCTGTCTAC[A/G]GGCGCCTTGTTGCGT	55658
rs3787010	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:661031	CAATCACTGTTCCAT[A/G]CTGGCTCCCTGGCCA	55658
rs3787011	snp	A/G	0.200492	0.245049	intron-variant	RNF126	GRCh38.p7	19:661080	GGCAAAGACCACAGC[A/G]GCCTGTCACCACAGA	55658
rs3787012	snp	C/T	0.499776	0.0105807	intron-variant	RNF126	GRCh38.p7	19:661781	AGCCGGGCGGCTACG[C/T]ACACAGCACAGTAAA	55658
rs3826951	snp	C/T	0.285519	0.247464	intron-variant	RNF126	GRCh38.p7	19:658092	ATCCATTCACCTCTC[C/T]GTCAGAGAACAGATG	55658
rs3826952	snp	A/C	0.314544	0.241524	intron-variant	RNF126	GRCh38.p7	19:661958	GTTTCCCCATCTATA[A/C]AGCACGGGTGGCTCG	55658
rs4594371	snp	A/G	0.474	0.111014	intron-variant	RNF126	GRCh38.p7	19:654968	gtgagactccgtatc[A/G]ggaaaaaaaaaaGTG	55658
rs4919820	snp	G/T	0.172997	0.237846	intron-variant	RNF126	GRCh38.p7	19:657588	CGCCCACCCTAGGGG[G/T]TTCAAAGGTCACCTC	55658
rs4919879	snp	A/C	0.486332	0.08153	intron-variant	RNF126	GRCh38.p7	19:651280	CACCAGGAGTGGGGC[A/C]CTGCGACGGCTCCCC	55658
rs4919880	snp	C/T	0.353587	0.22753	intron-variant	RNF126	GRCh38.p7	19:653830	GAAAATGGCCTCACA[C/T]GGCACGTGTCATCAC	55658
rs4919881	snp	C/T	0.166832	0.235761	intron-variant	RNF126	GRCh38.p7	19:656701	GCCAACGACCACCAC[C/T]GTGGCCCTGAGCTTA	55658
rs4919882	snp	C/T	0.16846	0.236329	intron-variant	RNF126	GRCh38.p7	19:662431	GAGGAACGCAGGCTC[C/T]GCTCACAAAGCCCCG	55658
rs4919883	snp	C/T	0.256897	0.249905	upstream-variant-2KB	RNF126	GRCh38.p7	19:664278	TTGAACTCCTGACCT[C/T]GTGATCCGCCCGCCT	55658
rs6510868	snp	C/T	0.453209	0.145623	intron-variant	RNF126	GRCh38.p7	19:655608	CCAGCCAGGACGAGA[C/T]GCAAGACCCCGTCAG	55658
rs6510873	snp	A/G	0.489083	0.0730708	upstream-variant-2KB	RNF126	GRCh38.p7	19:664931	CAGGCGTAAGCCACC[A/G]CGCCCGGCCTGCATT	55658
rs7245869	snp	C/T	0.286303	0.24735	intron-variant	RNF126	GRCh38.p7	19:659658	CTGGGTCTGCGCAGC[C/T]GCCTGTGGCCTGAGC	55658
rs7254550	snp	C/G/T	0.0225671	0.103817	intron-variant	RNF126	GRCh38.p7	19:648345	ggccgcggtcggggt[C/G/T]ggggggcgggtgggc	55658
rs7255896	snp	A/C	0.486984	0.079614	upstream-variant-2KB	RNF126	GRCh38.p7	19:663956	TAACCCCTGCTTCCA[A/C]ATTTAATCAGTAGAA	55658
rs7257070	snp	C/T	0.415727	0.187175	downstream-variant-500B	RNF126	GRCh38.p7	19:647486	CCCAGCTTGGCCTTT[C/T]CCTGACGCACGGGCG	55658
rs8100039	snp	C/G	0.0475351	0.146656	intron-variant	RNF126	GRCh38.p7	19:659469	TGGGGGGTCGGCAGG[C/G]AGAGCTGGAACCACC	55658
rs8102953	snp	A/G	0.0442142	0.141958	intron-variant	RNF126	GRCh38.p7	19:652206	AAGGCTGACACGATC[A/G]GGAAGCACGAGGGGC	55658
rs8113363	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB	RNF126	GRCh38.p7	19:664841	agacggggtttcact[A/G]tgttggccaggctgg	55658
rs10153505	snp	G/T	0.106633	0.204807	intron-variant	RNF126	GRCh38.p7	19:652948	GCAAACCCCCCCAAG[G/T]GTGAGGACAGAGGGG	55658
rs10401924	snp	C/T	0.0547245	0.156101	intron-variant	RNF126	GRCh38.p7	19:659623	CAGCTCCAGTCAGTG[C/T]CTCCTCAGCAGGCTC	55658
rs10408182	snp	G/T	0.0475351	0.146656	intron-variant	RNF126	GRCh38.p7	19:659907	tcactgggactacag[G/T]tgcctgccaccacgc	55658
rs10418071	snp	A/G	0.0887219	0.191022	intron-variant	RNF126	GRCh38.p7	19:648823	aaaatacaagtatga[A/G]ccaggcgtggcggcg	55658
rs10426061	snp	A/G	0.11968	0.213514	intron-variant	RNF126	GRCh38.p7	19:651343	CGTTTGACGACACGC[A/G]TGTGGACAGCAGTCT	55658
rs10601849	in-del	-/CT	0.157311	0.232183	intron-variant	RNF126	GRCh38.p7	19:660488	GCAGCAGTGCCGCCC[-/CT]GACTCAGCCGCCGGG	55658
rs11292816	in-del	-/A	0.28578	0.247426	intron-variant	RNF126	GRCh38.p7	19:655656	AAGTCCCCCAGATGG[-/A]ACTACCCCATGACCC	55658
rs11554788	snp	C/T	0.467539	0.123193	synonymous-codon	RNF126	GRCh38.p7	19:652238	CAGAGCCGGCCACCG[C/T]TGGAGGTGAGTCGCC	55658
rs11554790	snp	A/G/T	1.90984e-05	0.00309012	missense	RNF126	GRCh38.p7	19:651735	GCTGACGACGGCAGG[A/G/T]ACCCTGAGAGCCGGC	55658
rs12973146	snp	C/G	0.442385	0.15965	intron-variant	RNF126	GRCh38.p7	19:652739	CGGCCCCACACTCGG[C/G]GGGGCGGACGCCAGC	55658
rs12974698	snp	A/T			intron-variant	RNF126	GRCh38.p7	19:649829	ACTCACCAGGGGCCC[A/T]GGCTGGGGATGGGGA	55658
rs12976320	snp	C/G	0.486	0.0824865	intron-variant	RNF126	GRCh38.p7	19:649239	GGGGGGGGCCGCGCT[C/G]CTGAGTGCCCTGACG	55658
rs12981407	snp	C/G	0.317451	0.240729	intron-variant	RNF126	GRCh38.p7	19:653624	TGGATGGCTGGGCCC[C/G]TGGTGATGGCGGAGC	55658
rs12982248	snp	A/T	0.5	0	intron-variant	RNF126	GRCh38.p7	19:649856	GGGACAGGCACCCCC[A/T]CCTACTCACCAGGGA	55658
rs12982249	snp	C/T	0.5	0	intron-variant	RNF126	GRCh38.p7	19:649859	ACAGGCACCCCCTCC[C/T]ACTCACCAGGGACCC	55658
rs12984279	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:649825	CCCCACTCACCAGGG[A/G]CCCAGGCTGGGGATG	55658
rs17604088	snp	A/G	0.209693	0.246729	upstream-variant-2KB	RNF126	GRCh38.p7	19:665186	GGTTCAAACGACGCC[A/G]AACCACGAACTGGCT	55658
rs28418740	snp	C/T	0.0603597	0.1629	intron-variant	RNF126	GRCh38.p7	19:656990	AGGGGTAGCTCAGGG[C/T]TCAGGCTCTCCCTGC	55658
rs34088660	in-del	-/TT			intron-variant	RNF126	GRCh38.p7	19:655021	GCACCTGGCCTGGGC[-/TT]TTTTTTCTTTCTTTC	55658
rs34210228	in-del	-/C			intron-variant	RNF126	GRCh38.p7	19:659507	CCTTGCCCCTGACCT[-/C]CCCCGTCTCTGGGTG	55658
rs34323762	snp	A/G	0.304937	0.243889	intron-variant	RNF126	GRCh38.p7	19:658420	GCACAGCTTCCCGAG[A/G]GCCCTGCCACCCACA	55658
rs34495183	in-del	-/A			intron-variant	RNF126	GRCh38.p7	19:650609	GTGAAACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	55658
rs34538684	snp	A/G	0.296873	0.245566	intron-variant	RNF126	GRCh38.p7	19:653468	GCTGGGGAACTGTGA[A/G]CGTGGTTTTGGGACT	55658
rs34540044	in-del	-/A			downstream-variant-500B	RNF126	GRCh38.p7	19:647387	CCAGGGCCGGCTAGC[-/A]AAAACTGCTCTCCCG	55658
rs34930504	in-del	-/G			intron-variant	RNF126	GRCh38.p7	19:659702	CAGAGTGGGGCGTGT[-/G]GCGGCAGGAACCAGA	55658
rs35085693	snp	A/G	0.285519	0.247464	intron-variant	RNF126	GRCh38.p7	19:655434	CAGTGGCGCGATCTC[A/G]GCTCACTGCAAGCTC	55658
rs35233618	snp	A/G	0.362732	0.22314	intron-variant	RNF126	GRCh38.p7	19:654224	CCTCACGGTGGGTTC[A/G]TGTGCATCTGGCATC	55658
rs35641190	in-del	-/A			intron-variant	RNF126	GRCh38.p7	19:659782	AGCAAGACTCCTTCC[-/A]AAAAAAAAAAAAAAA	55658
rs35688047	in-del	-/G			intron-variant	RNF126	GRCh38.p7	19:657581	CCTTTGAACCCCCTA[-/G]GGTGGGCGTTCCAGC	55658
rs35831797	snp	G/T	0.5	0	intron-variant	RNF126	GRCh38.p7	19:659830	GTTGCAGTGAGCCGA[G/T]ATTGTGCCACTGCAG	55658
rs35891903	snp	A/C	0.0644444	0.167538	synonymous-codon	RNF126	GRCh38.p7	19:648943	AAACACAGGCCCCCC[A/C]CCGGCAGATAAAGAG	55658
rs35953948	in-del	-/C			intron-variant	RNF126	GRCh38.p7	19:651530	AATCCAGCACGGGTT[-/C]CCACGGAAACGTGGC	55658
rs55925830	snp	A/G	0.0792508	0.182605	intron-variant	RNF126	GRCh38.p7	19:649148	CCACGCGGCCCCCCC[A/G]CTCCTGGGTCCCCTG	55658
rs56044504	snp	C/G	0.0637235	0.166737	intron-variant	RNF126	GRCh38.p7	19:661726	AACTGCACTGCTTCT[C/G]GGGGGCTTGGACTTC	55658
rs56141012	in-del	-/AAAAAAAAAAA			intron-variant	RNF126	GRCh38.p7	19:654669	AAAAAAAAAAAAAAA[-/AAAAAAAAAAA]GTGCTGGCCGGGCGC	55658
rs56334730	in-del	-/GA	0.37778	0.214877	upstream-variant-2KB	RNF126	GRCh38.p7	19:664592	ATGAGGCATTGGAGC[-/GA]GACTGTTGAGGAATT	55658
rs56376239	snp	A/G	0.0733688	0.176922	downstream-variant-500B	RNF126	GRCh38.p7	19:647455	AGGACCGGACTCTGC[A/G]GAGCCCGACCAGCCT	55658
rs57115154	snp	A/G	0.108755	0.206276	upstream-variant-2KB	RNF126	GRCh38.p7	19:664210	CCACCACACCGGCTA[A/G]TTTTTGTATTTTTAG	55658
rs57869478	in-del	-/G	0.498016	0.0314335	intron-variant	RNF126	GRCh38.p7	19:658368	GACTGACAGTGACCA[-/G]GGGCAGGCAGGCCCC	55658
rs59145335	snp	A/G	0.0372196	0.131242	intron-variant	RNF126	GRCh38.p7	19:649268	CGGCGGAATGGGGGG[A/G]CCGTGCTCCGGCTGG	55658
rs59297411	snp	A/G	0.125528	0.21681	intron-variant	RNF126	GRCh38.p7	19:657397	GCACTGCCGGCTCAC[A/G]ACAGCCCGACCTGGC	55658
rs60101917	snp	A/G	0.367297	0.220775	intron-variant	RNF126	GRCh38.p7	19:658272	GCCCCTTCATCCACG[A/G]GGCCTGCACGGGGCG	55658
rs60873291	snp	A/G	0.084728	0.187577	intron-variant	RNF126	GRCh38.p7	19:652544	GTGGGTAGGGCCCCC[A/G]TGGCCCCTTCCCCGG	55658
rs61754469	snp	C/T	0.0390187	0.134115	missense, intron-variant	RNF126	GRCh38.p7	19:651684	CGCGGGGCTGTCGGG[C/T]GCCGTACCGGTGCCG	55658
rs62134273	snp	C/T	0.0162398	0.0886349	downstream-variant-500B	RNF126	GRCh38.p7	19:647445	CCCTGGAGACAGGAC[C/T]GGACTCTGCAGAGCC	55658
rs62134274	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:655636	CAGGCCTGCTGGGAG[C/T]CCAGAAGTCCCCCAG	55658
rs62134275	snp	C/G	0.5	0	intron-variant	RNF126	GRCh38.p7	19:656089	GGGTTCTTTTTGCAG[C/G]TGTGAGAATGCTGTG	55658
rs62134276	snp	A/T	0.5	0	intron-variant	RNF126	GRCh38.p7	19:660641	CCCAGCATAAAAAAT[A/T]CGTTTTTGAGACAGC	55658
rs67039359	in-del	-/GG	0	0	intron-variant	RNF126	GRCh38.p7	19:649221	GAATGGGGGGGGGGG[-/GG]CCGCGCTGCTGAGTG	55658
rs71335262	snp	C/T	0.5	0	intron-variant	RNF126	GRCh38.p7	19:654476	GGTGAAACTCTGTCT[C/T]TACTAAAAATACAAA	55658
rs71335263	snp	C/G	0.5	0	intron-variant	RNF126	GRCh38.p7	19:657272	TGGCACAGCGCTCGG[C/G]CGCTCTGGTCCCCAT	55658
rs72974187	snp	C/T	0.0554543	0.157009	intron-variant	RNF126	GRCh38.p7	19:652888	ACAGATATAATCCTG[C/T]AGGAGAGAACAGGAG	55658
rs72974191	snp	A/G	0.0581099	0.160244	intron-variant	RNF126	GRCh38.p7	19:653805	CTCAAGTGCTCCATC[A/G]CAGCAACGTGAAAAT	55658
rs72974194	snp	A/C	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:655798	ATCATCGTCGTCGGC[A/C]GATGCAAACAGCTCC	55658
rs72974200	snp	A/G	0.0663309	0.169604	intron-variant	RNF126	GRCh38.p7	19:662140	CCTGGGCAACACAGG[A/G]AGACCCCATTCCTAA	55658
rs73503983	snp	C/T	0.0260105	0.111035	intron-variant	RNF126	GRCh38.p7	19:652147	GCGGGCAGGGAGAGC[C/T]GGGGAGGCGAGGTGG	55658
rs73503985	snp	A/G	0.116634	0.211941	intron-variant	RNF126	GRCh38.p7	19:652700	GAGAAAAGTGCTCCC[A/G]GAGCCACAGACACCA	55658
rs73503987	snp	A/C	0.0490535	0.14873	intron-variant	RNF126	GRCh38.p7	19:658286	GGGGCCTGCACGGGG[A/C]GCATGTCCTGAGGGC	55658
rs73918170	snp	A/G	0.0023933	0.0345097	intron-variant	RNF126	GRCh38.p7	19:653301	CCCCGCACACAGCCC[A/G]TTCCCCTGGCTCGGG	55658
rs73918171	snp	C/T	0.0119091	0.0762411	intron-variant	RNF126	GRCh38.p7	19:661079	GGGCAAAGACCACAG[C/T]GGCCTGTCACCACAG	55658
rs73918172	snp	A/G	0.0023933	0.0345097	intron-variant	RNF126	GRCh38.p7	19:662247	AATAGCACCTTCAAC[A/G]AGCGCTGCTCCCACC	55658
rs74737028	snp	C/T	0.031825	0.122064	intron-variant	RNF126	GRCh38.p7	19:654268	GCACCATCTACAATA[C/T]AGAAAAAGTGCGGCC	55658
rs75066375	snp	A/G	0.00597247	0.0543191	intron-variant	RNF126	GRCh38.p7	19:652076	AACCAACCAAGCAGC[A/G]TGGGCCGCCCCAATC	55658
rs75309526	snp	C/G	0.0387552	0.1337	intron-variant	RNF126	GRCh38.p7	19:662214	ACTGACTCCGAAACC[C/G]TGGAAAAGGGGCCTG	55658
rs75659340	snp	C/T	0.000371058	0.0136158	intron-variant	RNF126	GRCh38.p7	19:652225	AGCACGAGGGGCGGG[C/T]GACTCACCTCCAACG	55658
rs75927396	snp	C/T	0.0803491	0.183626	intron-variant	RNF126	GRCh38.p7	19:661020	TAAATATTTGTCAAT[C/T]ACTGTTCCATGCTGG	55658
rs75962760	snp	C/T	0.0236746	0.106192	intron-variant	RNF126	GRCh38.p7	19:662159	CCCCATTCCTAAAAA[C/T]AATATTAGAAATGCA	55658
rs76785155	snp	C/T	0	0	intron-variant	RNF126	GRCh38.p7	19:659769	CCTCGTCATCGCCTT[C/T]TTTTTTTTTTTTTGG	55658
rs77045613	snp	C/T	0.5	0	upstream-variant-2KB	RNF126	GRCh38.p7	19:664249	CTAATTTTGGCATGT[C/T]GGCCAGGCTGGTCTT	55658
rs77160140	snp	A/G	0.0174175	0.0916809	intron-variant	RNF126	GRCh38.p7	19:655263	TGAGTCCAGGAGATC[A/G]AGACCGCAGTGAGCT	55658
rs77201994	snp	A/T			intron-variant	RNF126	GRCh38.p7	19:661006	CCAACGTCCATGATT[A/T]AATATTTGTCAATCA	55658
rs77392009	snp	G/T	0.5	0	intron-variant	RNF126	GRCh38.p7	19:660648	TAAAAAATTCGTTTT[G/T]GAGACAGCGTCTTGC	55658
rs77697994	snp	C/T	0.0535932	0.154675	intron-variant	RNF126	GRCh38.p7	19:656142	GCACAACTTTATGAA[C/T]ATACTACAAACGTTT	55658
rs78159499	snp	C/T	0.0607341	0.163335	intron-variant	RNF126	GRCh38.p7	19:653703	GGCCTCACCAGGGGC[C/T]GGGCAGATGCCGACA	55658
rs78804476	snp	A/G	0.00755907	0.0610114	intron-variant	RNF126	GRCh38.p7	19:662832	CTGCCTCCCGCCCGG[A/G]CCTCAGTCTCCCGCA	55658
rs79609574	snp	A/G	0.0126979	0.078662	intron-variant	RNF126	GRCh38.p7	19:660779	GCTGGGACTCCAGGA[A/G]TGCAACAACACACCC	55658
rs79915998	snp	C/T	0.00993419	0.0697739	intron-variant	RNF126	GRCh38.p7	19:653170	TTGGCTGAGCCCCTC[C/T]GACCTGCCCCACCGT	55658
rs79974336	snp	C/T	0.0221141	0.102801	intron-variant	RNF126	GRCh38.p7	19:658909	AGGTCCTCATGGTGG[C/T]AGAGTTCTAAGTGGG	55658
rs80005795	snp	C/T	0	0	intron-variant	RNF126	GRCh38.p7	19:659768	CCCTCGTCATCGCCT[C/T]TTTTTTTTTTTTTTG	55658
rs111227788	snp	C/T	0.0368353	0.130617	intron-variant	RNF126	GRCh38.p7	19:651102	ATCAACCGCCAGGAG[C/T]AGGGCCCTGCGACGG	55658
rs111304730	snp	C/T	0.00676609	0.0577691	intron-variant	RNF126	GRCh38.p7	19:656381	AAAAAGGGCTGGGCA[C/T]AGTGGCTCACACCTG	55658
rs111447017	snp	A/G	0.5	0	intron-variant	RNF126	GRCh38.p7	19:662651	CCGCGCCGCGCCACC[A/G]GGCAATACCCTCTCT	55658
rs111718327	in-del	-/T	0	0	intron-variant	RNF126	GRCh38.p7	19:657590	CCCACCCTAGGGGTT[-/T]CAAAGGTCACCTCTC	55658
rs111744804	snp	A/C	0.5	0	upstream-variant-2KB	RNF126	GRCh38.p7	19:663440	GGGGCGGGGCCGAGG[A/C]CCTCCTCCCCTCCCG	55658
rs111749235	snp	A/G	0.5	0	intron-variant	RNF126	GRCh38.p7	19:648737	ACTTTGGGAGGCCGA[A/G]GCAGGAGGATCACCT	55658
rs111801226	snp	C/T	0.095934	0.196885	intron-variant	RNF126	GRCh38.p7	19:650578	GAGGTCCACCACTCT[C/T]GGCTACTTTTTTTTT	55658
rs111907568	snp	A/G/T	0.00358779	0.0422022	intron-variant	RNF126	GRCh38.p7	19:654264	AGAGGCACCATCTAC[A/G/T]ATATAGAAAAAGTGC	55658
rs112092300	snp	A/G	0.5	0	intron-variant	RNF126	GRCh38.p7	19:653658	CCGAGCATTCGTGGG[A/G]CCTGGGCTGAAACGT	55658
rs112294311	snp	A/G	0.0524604	0.153226	intron-variant	RNF126	GRCh38.p7	19:650146	CTCCTACTCACCAGG[A/G]ACCCTGGCTGGGGAT	55658
rs112309446	snp	C/T	0.0513262	0.151752	intron-variant	RNF126	GRCh38.p7	19:650036	GATGGGGACAGGCAC[C/T]CCCACCCACTCACCA	55658
rs112598726	snp	A/C	0.5	0	intron-variant	RNF126	GRCh38.p7	19:658049	CAGAGGCCCCATTGG[A/C]GCCTCTGGCCCTAGC	55658
rs112728785	snp	C/T	0.00358779	0.0422022	intron-variant	RNF126	GRCh38.p7	19:652048	TCGGTGGAAGTTTCG[C/T]TTTCATCCAAGAAAC	55658
rs112846321	snp	A/G	0.5	0	intron-variant	RNF126	GRCh38.p7	19:649935	CAGGCTGGGGATGGG[A/G]ACAGGCACCCCCTCC	55658
rs112971888	snp	A/G	0.00358779	0.0422022	intron-variant	RNF126	GRCh38.p7	19:655327	AACCAGACCCTGCCA[A/G]AAAAAAAAAGAAAAA	55658
rs113168582	snp	C/T	0.5	0	intron-variant	RNF126	GRCh38.p7	19:651340	CAGCGTTTGACGACA[C/T]GCGTGTGGACAGCAG	55658
rs113207089	snp	A/C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:651328	CCAAGGCCTGGACAG[A/C/T]GTTTGACGACACGCG	55658
rs113396911	snp	A/G	0.5	0	intron-variant	RNF126	GRCh38.p7	19:655328	ACCAGACCCTGCCAA[A/G]AAAAAAAAGAAAAAG	55658
rs113485721	snp	A/G			downstream-variant-500B	RNF126	GRCh38.p7	19:647523	GAAAGCCACAGCACC[A/G]GCTTCTCTTTGTAAG	55658
rs113592844	snp	A/C	0.0490535	0.14873	intron-variant	RNF126	GRCh38.p7	19:658034	CACTGGGGGCCCCCA[A/C]AGAGGCCCCATTGGA	55658
rs113782750	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:655053	AGCAGCTCACACCTG[C/T]GATCCCAGTACTTTG	55658
rs113859521	snp	C/T	0.0614824	0.164198	intron-variant	RNF126	GRCh38.p7	19:652539	AGAATGTGGGTAGGG[C/T]CCCCGTGGCCCCTTC	55658
rs113961439	snp	A/G	0.104149	0.203046	intron-variant	RNF126	GRCh38.p7	19:657850	GTTGAGCCTCTGCTG[A/G]CCGACGGTGGGAGGG	55658
rs114047092	snp	A/G	0.0325976	0.123435	intron-variant	RNF126	GRCh38.p7	19:662515	GCCTGCCTCCAAGGC[A/G]GCGGCCAGGGCTCCA	55658
rs114177969	snp	C/T	0.0225045	0.103662	intron-variant	RNF126	GRCh38.p7	19:651049	AGCCACTTTTAAAGA[C/T]GACATTTCCAGCAGG	55658
rs114306307	snp	C/T	0.0228947	0.104514	intron-variant	RNF126	GRCh38.p7	19:659152	AGGCTGTCACTGTCA[C/T]GGTATCTGGCACAAC	55658
rs114314070	snp	C/G	0.123209	0.2158	intron-variant	RNF126	GRCh38.p7	19:662860	GCATGTACAGGACGG[C/G]GTTCGCGCGCGCACC	55658
rs114467127	snp	A/T	0.0244538	0.107838	intron-variant	RNF126	GRCh38.p7	19:651091	ACCATAAAAGCATCA[A/T]CCGCCAGGAGTAGGG	55658
rs114673942	snp	A/G	0.00318978	0.0398085	intron-variant	RNF126	GRCh38.p7	19:649390	AGGGCGCGACCTCTC[A/G]GGAAGAGGGACCGCG	55658
rs114742743	snp	A/G	0.109461	0.206758	utr-variant-3-prime	RNF126	GRCh38.p7	19:647711	GTGGCCCGTCCTGGC[A/G]GCACCTGCAGCACTG	55658
rs114867103	snp	A/G	0.00914312	0.0669923	intron-variant	RNF126	GRCh38.p7	19:655992	TGTCCAGGACAGGCC[A/G]AGCCACAGAGACAGA	55658
rs115017517	snp	A/G	0.00557542	0.0525036	intron-variant	RNF126	GRCh38.p7	19:653193	CCCACCGTGACGGGC[A/G]TCACCAGTGCCTGGG	55658
rs115151174	snp	A/G	0.0520825	0.152737	intron-variant	RNF126	GRCh38.p7	19:660846	TGCCACGTACGGAGA[A/G]GTTCTGACACTGCCA	55658
rs115211338	snp	C/T	0.0228947	0.104514	intron-variant	RNF126	GRCh38.p7	19:659524	GGTCAGGGGCAAGGA[C/T]GGCACGCAGGGCCAC	55658
rs115382924	snp	A/G	0.00579883	0.0535331	intron-variant	RNF126	GRCh38.p7	19:651927	GGCGCTAGGGCACAA[A/G]GACAAAGGAGAAAGC	55658
rs115431110	snp	A/C	0.0170251	0.090679	upstream-variant-2KB	RNF126	GRCh38.p7	19:664147	TGCCGAGGGTTCAAG[A/C]GATTCTCCCGCCTCA	55658
rs115586719	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653161	ATCAGCGCCTTGGCT[A/G]AGCCCCTCCGACCTG	55658
rs115726162	snp	A/C	0.0722614	0.17581	intron-variant	RNF126	GRCh38.p7	19:661140	AGGCCCAGTGACAGT[A/C]GGAGGAGGTCAAGGT	55658
rs115956072	snp	A/C	0.0150606	0.0854603	upstream-variant-2KB	RNF126	GRCh38.p7	19:665236	GCCTAACCTCTGAGA[A/C]GGCGGCAGAACCTGA	55658
rs116119469	snp	A/G	0.0345262	0.126772	intron-variant	RNF126	GRCh38.p7	19:660448	AGGCAGGAGCTTCCC[A/G]ACAGCCAGCCCAGGT	55658
rs116125090	snp	A/G	0.0228947	0.104514	utr-variant-3-prime	RNF126	GRCh38.p7	19:647665	CTACTCCGGGTCGTG[A/G]AGGCGGCCGAGGGGG	55658
rs116150192	snp	C/T	0.0189856	0.0955633	intron-variant	RNF126	GRCh38.p7	19:653478	CCACGTTCACAGTTC[C/T]CCAGCACCAGCCTCA	55658
rs116231824	snp	C/G	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:655865	GGAAAGGGGCAAGGC[C/G]CAGACCAGGCCACGG	55658
rs116322418	snp	C/G	0.0111196	0.0737302	intron-variant	RNF126	GRCh38.p7	19:660596	GGAGCAGCCGTCCCT[C/G]CCCAGAACAAACGCC	55658
rs116445499	snp	C/T	0.00159617	0.0282053	intron-variant	RNF126	GRCh38.p7	19:653445	CTGCCCAGGGACAGC[C/T]GTGGGTGAGTCCCAA	55658
rs116470650	snp	C/G	0.105968	0.204494	intron-variant	RNF126	GRCh38.p7	19:662327	CAGGAAGTAGCACTC[C/G]GCACGCCCAGGCCCA	55658
rs116680040	snp	A/G	0.105569	0.204058	intron-variant	RNF126	GRCh38.p7	19:651543	TGGAACCCGTGCTGG[A/G]TTCTAAGCGCCAGAA	55658
rs116754142	snp	A/G	0.00159617	0.0282053	intron-variant	RNF126	GRCh38.p7	19:657021	ATGGTGACTCCCCAG[A/G]CTAGCACCACCCAGT	55658
rs116941761	snp	C/T	0.0252325	0.109451	intron-variant	RNF126	GRCh38.p7	19:658335	AGGGGAGTGGGCTGG[C/T]GACCTACAGGCCCCA	55658
rs117066118	snp	A/G	0.00597247	0.0543191	intron-variant	RNF126	GRCh38.p7	19:657774	GGGCCACCGAAGGCC[A/G]GAACCGAGGCTCTGG	55658
rs117074311	snp	C/T	0.128664	0.218581	intron-variant	RNF126	GRCh38.p7	19:651587	GGCGTGGGGCCCTCG[C/T]GGCCACCCCCGGGGC	55658
rs117231919	snp	C/T	0.0337553	0.125452	intron-variant	RNF126	GRCh38.p7	19:652628	CAGGTTGCCGGCACT[C/T]CCCTCTGGCCCCGGC	55658
rs117264382	snp	A/C	0.00398564	0.0444627	intron-variant	RNF126	GRCh38.p7	19:659431	CACTTGGGGACACTG[A/C]GGAGGTTGCAGGCGT	55658
rs117449402	snp	C/T	0.00398564	0.0444627	intron-variant	RNF126	GRCh38.p7	19:657742	GCTGTCTCTCAGGCC[C/T]CCGGCCAGCCCCTCC	55658
rs117571434	snp	G/T	0.00993419	0.0697739	intron-variant	RNF126	GRCh38.p7	19:652522	ACAGCCTCCTAAGCG[G/T]GAGAATGTGGGTAGG	55658
rs117693135	snp	C/T	0.0295035	0.117819	intron-variant	RNF126	GRCh38.p7	19:653686	CGTGCATGGTGCCTC[C/T]CGGCCTCACCAGGGG	55658
rs117952367	snp	A/G	0.0383715	0.133092	intron-variant	RNF126	GRCh38.p7	19:656865	CCCCTGGTTTCTGCC[A/G]GTGTCGGGTCTATCG	55658
rs118107804	snp	A/G	0.0162398	0.0886349	downstream-variant-500B	RNF126	GRCh38.p7	19:647462	GACTCTGCAGAGCCC[A/G]ACCAGCCTCCCAGCT	55658
rs118167041	snp	A/G	0.00517822	0.0506191	intron-variant	RNF126	GRCh38.p7	19:660930	CTTGGGATCACCCGC[A/G]GGGTGGACACGGGCA	55658
rs137868233	snp	A/G	0.00159617	0.0282053	intron-variant	RNF126	GRCh38.p7	19:655709	GGCGCAGACCCCAGA[A/G]AAACGAAGACACCTG	55658
rs137946000	snp	A/G	0.000179692	0.00947702	synonymous-codon	RNF126	GRCh38.p7	19:648901	GTGCTCCTCAGTGAC[A/G]GGGACGGTGGGGAGG	55658
rs138235228	in-del	-/G	0.0836354	0.186609	intron-variant	RNF126	GRCh38.p7	19:655502	AAAAAAAAGAAAAGT[-/G]GGGGGGGAAAGGACG	55658
rs138500516	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:653409	CCAACATGGTGATGT[C/T]CCAGAGGAGACGTGA	55658
rs138581411	snp	C/T	5.30574e-05	0.00515033	missense	RNF126	GRCh38.p7	19:650268	TGGTGGCGGGCGTGA[C/T]GATGCCGTTGACGAG	55658
rs138633729	snp	A/G	0.000839158	0.0204664	missense	RNF126	GRCh38.p7	19:652838	TACCTGGTCTCTTCC[A/G]GAAGCTCCTCGATAA	55658
rs138719773	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:656633	AGCCTGGGCCACAGA[A/G]TGAGACCGTGTCAGA	55658
rs138868462	snp	C/G/T	0.000348527	0.0131965	missense	RNF126	GRCh38.p7	19:651722	TGGTCTCTCTCCCGC[C/G/T]GGCTCTCAGGGTCCC	55658
rs139160794	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	RNF126	GRCh38.p7	19:663934	GGTGCGGAGAAGGCA[G/T]GAAACCTAACCCCTG	55658
rs139272504	snp	A/G	0.00358779	0.0422022	intron-variant	RNF126	GRCh38.p7	19:658703	CTGGATGGACGAGGC[A/G]TGAGCGAAGCCACTG	55658
rs139564628	snp	A/C/T	0.00579914	0.0535352	synonymous-codon	RNF126	GRCh38.p7	19:651754	GCCGTCGTCAGCCTG[A/C/T]GCCCCAGGAGGGAAC	55658
rs139851549	snp	C/T	0.000290169	0.0120416	missense	RNF126	GRCh38.p7	19:651816	CGAAAGCAAACTGTC[C/T]GTAGCCCTGCGGCAG	55658
rs139977372	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:654362	ACGCTCCGCCATCAC[C/T]GGGGGCGCGGTGGCT	55658
rs140074299	snp	G/T	0.0119091	0.0762411	intron-variant	RNF126	GRCh38.p7	19:659625	TCGAGCCTGCTGAGG[G/T]GGCACTGACTGGAGC	55658
rs140144851	snp	C/T	0.0240643	0.107019	intron-variant	RNF126	GRCh38.p7	19:649165	TCCTGGGTCCCCTGA[C/T]GGTGGAATGGGGGAA	55658
rs140252063	snp	C/T	9.00406e-05	0.00670911	synonymous-codon	RNF126	GRCh38.p7	19:652870	ACCAGACTCGCATCT[C/T]GGACAGATATAATCC	55658
rs140568052	snp	A/G/T	0.000399281	0.0141238	upstream-variant-2KB	RNF126	GRCh38.p7	19:664548	CTGAGGGATGAATAG[A/G/T]ATTTGGTTGGAGTTG	55658
rs140879471	snp	A/G	0.000155521	0.00881682	synonymous-codon	RNF126	GRCh38.p7	19:649703	GATGGCATCCAGGCC[A/G]TTGGCCCCCCAGGCG	55658
rs141021872	in-del	-/AAG	0.120326	0.21374	intron-variant	RNF126	GRCh38.p7	19:655012	AGAAAGAAAGAAAGA[-/AAG]AAAAAAAAGCCCAGG	55658
rs141041527	snp	A/G	0.00874735	0.0655527	intron-variant	RNF126	GRCh38.p7	19:655225	GAGACAGGCAGGAGC[A/G]GGAGGCAGGAGGCAG	55658
rs141130751	snp	A/G	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:652606	CTGAGGGAGGTGAGC[A/G]GCTGCACAGGTTGCC	55658
rs141143351	snp	C/T	0.00159617	0.0282053	intron-variant	RNF126	GRCh38.p7	19:651342	GCGTTTGACGACACG[C/T]GTGTGGACAGCAGTC	55658
rs141561227	snp	C/T	0.0263992	0.111815	intron-variant	RNF126	GRCh38.p7	19:658398	CTGGTGACAGTGACT[C/T]GGCCCCTGTGGGTGG	55658
rs141579962	in-del	-/GT	0.0379877	0.132479	intron-variant	RNF126	GRCh38.p7	19:648697	TCGAGGCCGGGTGCG[-/GT]GTGGCTCACGCCTGT	55658
rs141666169	snp	C/T	0.0130921	0.0798413	intron-variant	RNF126	GRCh38.p7	19:652976	GGGCTCCGGACCCAG[C/T]GGTCTCTGGCTGGCC	55658
rs141916909	snp	C/T	0.000611797	0.0174792	missense	RNF126	GRCh38.p7	19:651741	TCTCAGGGTCCCTGC[C/T]GTCGTCAGCCTGCGC	55658
rs141943222	snp	C/T	0.0023933	0.0345097	intron-variant	RNF126	GRCh38.p7	19:656138	GGTTGCACAACTTTA[C/T]GAATATACTACAAAC	55658
rs142002356	snp	C/T	0.0966517	0.197444	intron-variant	RNF126	GRCh38.p7	19:662932	CGAGCCTCAGTTTTC[C/T]CGTCGTGGTCAGCTC	55658
rs142270932	snp	C/T	0.0023933	0.0345097	intron-variant	RNF126	GRCh38.p7	19:652129	AAAAATTTCCTCCGC[C/T]GTGCGGGCAGGGAGA	55658
rs142393586	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:648982	ATTGAGGAGCTGAAA[A/G]ACAAGAGGCGAGAGT	55658
rs142619184	snp	A/T	0.0368353	0.130617	intron-variant	RNF126	GRCh38.p7	19:651110	CCAGGAGTAGGGCCC[A/T]GCGACGGCTCCCCCA	55658
rs142724625	snp	C/T	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:660054	ACAGGCGTGAGCCAC[C/T]GCGCTCGGCCTCATC	55658
rs142744250	snp	C/T	0.00478085	0.0486577	intron-variant	RNF126	GRCh38.p7	19:658743	AGGCTGGGGCCCCGC[C/T]TCACACCCCAGGGCG	55658
rs142966806	snp	C/T	5.1216e-05	0.00506017	missense	RNF126	GRCh38.p7	19:651780	GGAACGTGGGGATCT[C/T]GAAGCTGTCATCGAA	55658
rs143060769	snp	C/G	0.000798403	0.0199641	synonymous-codon	RNF126	GRCh38.p7	19:648185	GGAGGACGATGACGA[C/G]GAGGAGGAGAAGCTC	55658
rs143168811	snp	A/G	4.46259e-05	0.00472345	missense	RNF126	GRCh38.p7	19:652276	GGAGCTGTGGAGGGG[A/G]CAGAACCATTTTCTG	55658
rs143387909	snp	A/G	0.00835141	0.0640778	intron-variant	RNF126	GRCh38.p7	19:659758	CACCCAGACACCCTC[A/G]TCATCGCCTTTTTTT	55658
rs143441978	snp	C/T	0.00666612	0.0573465	intron-variant	RNF126	GRCh38.p7	19:652916	GAGGCCGGGTCACGG[C/T]GACGCCGGCATCACC	55658
rs143546424	snp	C/T	0.0138799	0.0821421	intron-variant	RNF126	GRCh38.p7	19:651004	AGAGAACTGCAAATA[C/T]AGCACTGAGCCACCG	55658
rs143834948	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:661486	TCTCAGCTCCCCAAC[C/T]TTCGCCCCACACCCG	55658
rs143968736	snp	A/G	0.00279162	0.0372561	intron-variant	RNF126	GRCh38.p7	19:653653	GCGTGCCGAGCATTC[A/G]TGGGGCCTGGGCTGA	55658
rs143978135	snp	A/G	0.00755907	0.0610114	intron-variant	RNF126	GRCh38.p7	19:661709	GGTCTCTACTCCCGG[A/G]GAACTGCACTGCTTC	55658
rs144204924	snp	C/T	0.0111196	0.0737302	upstream-variant-2KB	RNF126	GRCh38.p7	19:664907	CGGCCTGCCATAGTG[C/T]TGGGATTACAGGCGT	55658
rs144257905	snp	A/G	0.0287284	0.116357	intron-variant	RNF126	GRCh38.p7	19:654828	AAATGTTAGCCAGGC[A/G]TGGTGGCACGTACCT	55658
rs144316449	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:656852	AGTCAAATCTGAACC[C/T]CTGGTTTCTGCCGGT	55658
rs144347019	snp	A/G	0.00283895	0.0375688	utr-variant-3-prime	RNF126	GRCh38.p7	19:648119	GCTTTCCCGACGGCC[A/G]ACGTGGGCTCACGAG	55658
rs144653786	snp	C/T	0.0107286	0.0724924	intron-variant	RNF126	GRCh38.p7	19:654499	AATACAAAAATTAGC[C/T]GGGTGTGGTGGCGGG	55658
rs144919681	snp	A/G	0.0165839	0.0895372	intron-variant	RNF126	GRCh38.p7	19:652816	CCTCTTCAACAGGGG[A/G]CTGCATTACCTGGTC	55658
rs145178688	snp	A/G	5.2694e-05	0.00513266	synonymous-codon	RNF126	GRCh38.p7	19:651853	CAGGTGCTGGTCCAC[A/G]TGCTGGGGAGAGGAG	55658
rs145351023	snp	C/T	0.0126979	0.078662	intron-variant	RNF126	GRCh38.p7	19:649593	ACCTTTGTGGGGCTT[C/T]GTGGGTCCAGGCAGT	55658
rs145549398	snp	C/G	0.0513262	0.151752	intron-variant	RNF126	GRCh38.p7	19:659832	GCAGTGGCACAATCT[C/G]GGCTCACTGCAACCT	55658
rs145622887	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:652082	CCAAGCAGCGTGGGC[C/T]GCCCCAATCCCTGGC	55658
rs145749823	snp	A/G	7.76307e-05	0.00622971	intron-variant	RNF126	GRCh38.p7	19:650344	CCGCCCCACGCACAG[A/G]AGAGGCGCCAGGCCT	55658
rs145757345	snp	A/T			intron-variant	RNF126	GRCh38.p7	19:660802	ACACACCCCACTAAT[A/T]GTTTTAGTCTTCTGT	55658
rs146100371	in-del	-/TTTG	0.0566837	0.158521	upstream-variant-2KB	RNF126	GRCh38.p7	19:664637	TGTGCATTTAGATTT[-/TTTG]TTTGTTTGTTTGTTT	55658
rs146299332	snp	C/T	0.000254944	0.0112875	missense	RNF126	GRCh38.p7	19:651744	CAGGGTCCCTGCCGT[C/T]GTCAGCCTGCGCCCC	55658
rs146478740	snp	A/G	0.00517822	0.0506191	intron-variant	RNF126	GRCh38.p7	19:652584	GTCACCAGATTAGCC[A/G]CCGAGGCTGAGGGAG	55658
rs146573278	snp	A/G	0.00159617	0.0282053	intron-variant	RNF126	GRCh38.p7	19:654922	CAACGAGCCGAGATC[A/G]TGACATTGTAACTCC	55658
rs146932907	snp	A/G/T	0.00018483	0.00961183	missense, synonymous-codon	RNF126	GRCh38.p7	19:648399	GGGCACGATGCAGCC[A/G/T]TCGTGGAACAGGTGG	55658
rs147338370	snp	A/C	0.00597247	0.0543191	intron-variant	RNF126	GRCh38.p7	19:654249	GTGAGGGGAGAGTGA[A/C]GAGGCACCATCTACA	55658
rs147496504	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652067	CATCCAAGAAACCAA[C/T]CAAGCAGCGTGGGCC	55658
rs147513802	snp	A/G/T	0.00716521	0.0594565	intron-variant	RNF126	GRCh38.p7	19:653125	CGACCTGGCCCCACC[A/G/T]TGACGGGCGTCACCA	55658
rs147659622	snp	A/G	0.00100549	0.0223994	intron-variant	RNF126	GRCh38.p7	19:650193	ACCCACTCACCAGGG[A/G]CCCAGGCTGGGGATG	55658
rs147741026	snp	A/C	0.0150606	0.0854603	intron-variant	RNF126	GRCh38.p7	19:652122	TGGAGGGAAAAATTT[A/C]CTCCGCCGTGCGGGC	55658
rs147764244	snp	C/T	0.00597247	0.0543191	upstream-variant-2KB	RNF126	GRCh38.p7	19:665252	GGCGGCAGAACCTGA[C/T]GGTTTTCCGTTGGCT	55658
rs147786640	snp	C/T	0.0016157	0.0283768	synonymous-codon	RNF126	GRCh38.p7	19:651832	GTAGCCCTGCGGCAG[C/T]GTGAACAGGTGCTGG	55658
rs147792006	snp	A/T	0.00624173	0.0555149	intron-variant	RNF126	GRCh38.p7	19:650197	ACTCACCAGGGACCC[A/T]GGCTGGGGATGGGGA	55658
rs147800167	snp	C/G	0.00318978	0.0398085	intron-variant	RNF126	GRCh38.p7	19:661032	AATCACTGTTCCATG[C/G]TGGCTCCCTGGCCAG	55658
rs147803444	snp	A/G	0.00031181	0.0124823	synonymous-codon	RNF126	GRCh38.p7	19:648194	TGACGACGAGGAGGA[A/G]AAGCTCACCCCAGTG	55658
rs148007786	snp	A/G	0.0023933	0.0345097	intron-variant	RNF126	GRCh38.p7	19:652968	GGACAGAGGGGCTCC[A/G]GACCCAGCGGTCTCT	55658
rs148485155	snp	C/G	0.00676609	0.0577691	intron-variant	RNF126	GRCh38.p7	19:659990	GGCTGGTCTCGAACT[C/G]CTGACCTCAGGTGAT	55658
rs148540129	snp	C/T	0.0232847	0.105357	intron-variant	RNF126	GRCh38.p7	19:654637	GAGGGAGCAAGACTC[C/T]GTCTCAAAAAAAAAA	55658
rs148724293	snp	C/T	0.0158469	0.0875917	intron-variant	RNF126	GRCh38.p7	19:652126	GGGAAAAATTTCCTC[C/T]GCCGTGCGGGCAGGG	55658
rs148780110	snp	G/T	0.00578699	0.053479	intron-variant	RNF126	GRCh38.p7	19:648535	CGTGGGGGGCCTGCC[G/T]AGCCTTCAAGGGCAG	55658
rs148837267	snp	A/G	5.76253e-05	0.00536743	intron-variant	RNF126	GRCh38.p7	19:652901	TGCAGGAGAGAACAG[A/G]AGGCCGGGTCACGGT	55658
rs148889056	snp	C/G	0.0023933	0.0345097	intron-variant	RNF126	GRCh38.p7	19:650488	AGCAGCTTGATCTTG[C/G]TTCACTGCAGCCCCA	55658
rs149042780	snp	C/T	0.00029549	0.0121514	synonymous-codon	RNF126	GRCh38.p7	19:652239	GCGACTCACCTCCAA[C/T]GGTGGCCGGCTCTGG	55658
rs149302407	snp	A/C/T	0.000373684	0.0136643	missense	RNF126	GRCh38.p7	19:651692	TGTCGGGCGCCGTAC[A/C/T]GGTGCCGGGACGGAT	55658
rs149399922	snp	A/C	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:661263	GAGTCAAGGCAGTGT[A/C]GGCCCCCCACAGCCA	55658
rs149405763	snp	A/G	0.00298173	0.0384964	missense	RNF126	GRCh38.p7	19:651704	TACCGGTGCCGGGAC[A/G]GATGGTCTCTCTCCC	55658
rs149774599	snp	A/G	0.00953873	0.0683987	intron-variant	RNF126	GRCh38.p7	19:654369	GCCATCACCGGGGGC[A/G]CGGTGGCTCAGGCCT	55658
rs149825528	snp	A/G	8.53322e-05	0.00653137	synonymous-codon	RNF126	GRCh38.p7	19:651817	GAAAGCAAACTGTCC[A/G]TAGCCCTGCGGCAGC	55658
rs150175128	snp	A/G	0.000960922	0.0218983	synonymous-codon	RNF126	GRCh38.p7	19:650260	GCTGGGGATGGTGGC[A/G]GGCGTGATGATGCCG	55658
rs150227930	snp	A/G	5.93489e-05	0.0054471	intron-variant	RNF126	GRCh38.p7	19:650309	ATCCTGGAAAAGAGA[A/G]CGCCAGTCACGGGGT	55658
rs150247440	in-del	-/GTCCTCTCA			intron-variant	RNF126	GRCh38.p7	19:659403	CCCAGCACCCCCACC[-/GTCCTCTCA]CCGCCACTTGGGGAC	55658
rs150250908	snp	A/G	0.0240643	0.107019	intron-variant	RNF126	GRCh38.p7	19:661180	CCAAGGCCACGGGGC[A/G]AGGAAGTGGCTCCAC	55658
rs150302090	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:655673	CTACCCCATGACCCA[C/T]GAGCTAGAACTTTCA	55658
rs150696750	snp	A/G	0.000136073	0.0082473	synonymous-codon	RNF126	GRCh38.p7	19:651790	GATCTCGAAGCTGTC[A/G]TCGAAGATGCCGAAA	55658
rs150753457	snp	A/G	0.0456336	0.143994	intron-variant	RNF126	GRCh38.p7	19:651388	CCTGGCAGGCACACG[A/G]TGCCCCACTCTGTGG	55658
rs150829232	snp	A/G	0.0248432	0.108648	intron-variant	RNF126	GRCh38.p7	19:658560	CAGTGTGTGGGCCCC[A/G]CAGCCCCAGAGGCAC	55658
rs150846518	snp	G/T	0.00795532	0.062565	upstream-variant-2KB	RNF126	GRCh38.p7	19:663679	CCCTCCTGCTCCGTG[G/T]CACTGATTCCCTCCC	55658
rs151004072	snp	C/G	0.0023933	0.0345097	intron-variant	RNF126	GRCh38.p7	19:660706	ACCATCACGGCTCAC[C/G]GCAGCCTCCACCTCC	55658
rs151233237	snp	C/T	0.00358779	0.0422022	intron-variant	RNF126	GRCh38.p7	19:655464	GCACTCTAGCCCGGG[C/T]GACAGAGTGACACTC	55658
rs180829677	snp	A/G	0.00835141	0.0640778	intron-variant	RNF126	GRCh38.p7	19:648685	TTCAGGGAAATGCTC[A/G]AGGCCGGGTGCGGTG	55658
rs180831298	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	RNF126	GRCh38.p7	19:664340	GAGCCACCGCGCCCG[G/T]CCTCATGCGTGTATT	55658
rs180969314	snp	C/G	0.00199481	0.0315187	intron-variant	RNF126	GRCh38.p7	19:652055	AAGTTTCGCTTTCAT[C/G]CAAGAAACCAACCAA	55658
rs181014079	snp	C/T	0.00199481	0.0315187	intron-variant	RNF126	GRCh38.p7	19:658550	GGCTGATCCACAGTG[C/T]GTGGGCCCCGCAGCC	55658
rs181586380	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:658323	CCAGGCGCATGGAGG[A/G]GAGTGGGCTGGCGAC	55658
rs181797268	snp	A/G	0.00199481	0.0315187	intron-variant	RNF126	GRCh38.p7	19:654742	GAGGCCGAGGCAGGC[A/G]AATCACCTGAGGCCA	55658
rs181843600	snp	C/T	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:649381	AAGCAGGTCAGGGCG[C/T]GACCTCTCGGGAAGA	55658
rs181968881	snp	A/G	0.00318978	0.0398085	upstream-variant-2KB	RNF126	GRCh38.p7	19:664102	GGCTGGGGTGCAATG[A/G]CCCGATCTCGGCTCA	55658
rs182058847	snp	C/T	0.00478085	0.0486577	upstream-variant-2KB	RNF126	GRCh38.p7	19:664740	TCCGCCTCCCGGGTT[C/T]AAGTGATTCTCCTGC	55658
rs182206628	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:650521	CTGCTGGGCTTAAGC[A/G]ATCCTCCCGCCTCAG	55658
rs182246420	snp	C/G/T	0.00976173	0.0691849	intron-variant	RNF126	GRCh38.p7	19:648523	GGTCACAGCGGGCGT[C/G/T]GGGGGCCTGCCGAGC	55658
rs182362294	snp	A/G	0.00358779	0.0422022	intron-variant	RNF126	GRCh38.p7	19:652421	TGCTTCCCACCCGCC[A/G]CCGCCCCAGCATTTG	55658
rs182534471	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:654899	TTGAACCTAGGAGGC[A/G]GAGGCTGCAACGAGC	55658
rs182961039	snp	A/G	0.00676609	0.0577691	intron-variant	RNF126	GRCh38.p7	19:655419	TGAACCTGGGAGGCA[A/G]AGCTTGCAGTGAGCC	55658
rs183068476	snp	A/G	0.00874735	0.0655527	intron-variant	RNF126	GRCh38.p7	19:652745	CACACTCGGCGGGGC[A/G]GACGCCAGCACAGCC	55658
rs183079959	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:656572	AGAATCGCTTAAACC[C/T]GGCAGGCAGAGGTTG	55658
rs183405749	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:660306	GAATGACCCAGCTGC[A/G/T]CGGGGCCTCAGCCTG	55658
rs183561932	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652075	AAACCAACCAAGCAG[C/T]GTGGGCCGCCCCAAT	55658
rs183645794	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:648526	CACAGCGGGCGTGGG[A/G]GGCCTGCCGAGCCTT	55658
rs183646991	snp	A/G	0.00795532	0.062565	upstream-variant-2KB	RNF126	GRCh38.p7	19:664948	GCCCGGCCTGCATTT[A/G]GGGTTTTGAATGTCC	55658
rs183678293	snp	C/T	0.00438332	0.0466095	intron-variant	RNF126	GRCh38.p7	19:653631	CTGGGCCCCTGGTGA[C/T]GGCGGAGCGTGCCGA	55658
rs184220578	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:656815	GATTGGGACGCCCCA[C/T]GTAAACACGCTGAGA	55658
rs184337072	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:662203	ATTCCACACCTACTG[A/C]CTCCGAAACCCTGGA	55658
rs184522181	snp	A/G	0.00279162	0.0372561	upstream-variant-2KB	RNF126	GRCh38.p7	19:664286	CTGACCTCGTGATCC[A/G]CCCGCCTCGGCCTCC	55658
rs184566113	snp	C/T	0.00279162	0.0372561	intron-variant	RNF126	GRCh38.p7	19:657724	GTATTGTCAGGGCTC[C/T]GGGCTGTCTCTCAGG	55658
rs185079707	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:653937	GCATGGGGGAGTGCT[A/G]TGAGGGGAGCCAAGG	55658
rs185089307	snp	A/T	0.00358779	0.0422022	upstream-variant-2KB	RNF126	GRCh38.p7	19:664074	TTGAGACGGAGTCTC[A/T]CTCTGTCACCCAGGC	55658
rs185184773	snp	C/T	0.000371264	0.0136196	utr-variant-3-prime	RNF126	GRCh38.p7	19:647879	CTTTCCACCGCTGAA[C/T]GTTTAGAGGGTGAGG	55658
rs185230177	snp	A/G	0.00557542	0.0525036	intron-variant	RNF126	GRCh38.p7	19:651548	CCCGTGCTGGATTCT[A/G]AGCGCCAGAACTTCC	55658
rs185637142	snp	C/T	0.00358779	0.0422022	intron-variant	RNF126	GRCh38.p7	19:648696	GCTCGAGGCCGGGTG[C/T]GGTGGCTCACGCCTG	55658
rs185639349	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF126	GRCh38.p7	19:664459	GACAGGAGCGTGGAA[C/T]TCAAGGGTGACTCTG	55658
rs185843677	snp	G/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:658709	GGACGAGGCGTGAGC[G/T]AAGCCACTGCCTCAG	55658
rs185891316	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:660106	TGCTGCCCCTGTGCC[A/G]TCGTCGCCTGAGCCC	55658
rs185946235	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652424	TTCCCACCCGCCACC[A/G]CCCCAGCATTTGGTG	55658
rs185966470	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:654872	CTCAGGAGGCTGAGA[C/T]AGGAGAATCGCTTGA	55658
rs185971891	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:654300	GGCTCCTGGTGAGGC[C/T]GGGAGGCACCACATG	55658
rs186536892	snp	A/G			missense	RNF126	GRCh38.p7	19:652261	CGGCTCTGGTCTGTG[A/G]GAGCTGTGGAGGGGG	55658
rs186590078	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF126	GRCh38.p7	19:664804	GGCACCACCACGCCC[A/G]CCTAATTTTTGTATT	55658
rs186627298	snp	G/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:661078	AGGGCAAAGACCACA[G/T]CGGCCTGTCACCACA	55658
rs186709306	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:655320	GTGACAGAACCAGAC[A/C]CTGCCAAAAAAAAAA	55658
rs186800635	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652166	GAGGCGAGGTGGGGA[C/T]AGGCTGGCGCTCGGG	55658
rs186811734	snp	A/G	0.00597247	0.0543191	intron-variant	RNF126	GRCh38.p7	19:650369	AGGCCTGCCAGGTCC[A/G]TGGTGAGCACCAAGG	55658
rs186863781	snp	C/T	8.87745e-05	0.00666178	intron-variant	RNF126	GRCh38.p7	19:649781	GGTTCAAGTGGCTGA[C/T]GGGCAGCTGGGGCAG	55658
rs187118822	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	RNF126	GRCh38.p7	19:647112	AACCCACTGCCCCGG[A/C]CCCCTGAGCCCGCAG	55658
rs187121297	snp	G/T			intron-variant	RNF126	GRCh38.p7	19:662314	TGCCCTAAACGAGCA[G/T]GAAGTAGCACTCGGC	55658
rs187261285	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:650927	AGAGATGGGGCCTCC[C/T]TACATTGCTCAGGCT	55658
rs187264853	snp	A/G	0.00318978	0.0398085	intron-variant	RNF126	GRCh38.p7	19:655893	CGGCGGGGGGGAGGG[A/G]GGATTGCATCTTGAG	55658
rs187640705	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:658354	CTACAGGCCCCAGAT[A/G]ACTGACAGTGACCAG	55658
rs187867666	snp	A/G	0.00993419	0.0697739	intron-variant	RNF126	GRCh38.p7	19:653314	CCGTTCCCCTGGCTC[A/G]GGGGAGGCCACGTCC	55658
rs187881104	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	RNF126	GRCh38.p7	19:665049	CTCTGACCACCAGAG[A/G]GCGCACGGGCCCCGT	55658
rs187959872	snp	C/T	0.000289101	0.0120194	intron-variant	RNF126	GRCh38.p7	19:648534	GCGTGGGGGGCCTGC[C/T]GAGCCTTCAAGGGCA	55658
rs187964788	snp	A/G	0.00478085	0.0486577	intron-variant	RNF126	GRCh38.p7	19:652977	GGCTCCGGACCCAGC[A/G]GTCTCTGGCTGGCCA	55658
rs187975452	snp	C/T	0.00478085	0.0486577	upstream-variant-2KB	RNF126	GRCh38.p7	19:664334	AGGCATGAGCCACCG[C/T]GCCCGGCCTCATGCG	55658
rs188499201	snp	C/G	0.000109022	0.00738234	intron-variant	RNF126	GRCh38.p7	19:651569	CAGAACTTCCGACCT[C/G]AAGGCGTGGGGCCCT	55658
rs188770543	snp	A/G	0.00318978	0.0398085	intron-variant	RNF126	GRCh38.p7	19:656660	CAGAAAAAGAAAAAG[A/G]AAAAGGGAAAGGGGA	55658
rs188884260	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:657963	GCTGCAGGTAGAAAC[A/G]CCTGGGCAAGGGGGC	55658
rs189159238	snp	A/G	0.00159617	0.0282053	intron-variant	RNF126	GRCh38.p7	19:660679	TTGTCACCCAGGCTG[A/G]AGTGCACTGGCACCA	55658
rs189293416	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:651981	GGTGGGAGGGAGACG[C/G]AGACAGGGAGGCAGG	55658
rs189306354	snp	A/G	0.00398564	0.0444627	intron-variant	RNF126	GRCh38.p7	19:653715	GGCTGGGCAGATGCC[A/G]ACACACACTTCCCGC	55658
rs189499664	snp	G/T	0.00279162	0.0372561	intron-variant	RNF126	GRCh38.p7	19:654219	CAAACGATGCCAGAT[G/T]CACATGAACCCACCG	55658
rs189516478	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:654569	AATTGCTTGAGCCCG[A/G]GAGGCGGAGGTTGCA	55658
rs189679508	snp	C/T	0.00557542	0.0525036	intron-variant	RNF126	GRCh38.p7	19:652103	AATCCCTGGCCCGGG[C/T]CCCTGGAGGGAAAAA	55658
rs189920379	snp	C/T	0.0115144	0.0749975	intron-variant	RNF126	GRCh38.p7	19:656879	CGGTGTCGGGTCTAT[C/T]GGGGCTCCTCTGGGC	55658
rs190000476	snp	A/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:650504	TTCACTGCAGCCCCA[A/T]CCTGCTGGGCTTAAG	55658
rs190013748	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RNF126	GRCh38.p7	19:664510	GAGAGGGCTTCCGAG[C/G]GGTAAGGACATTGGA	55658
rs190022317	snp	C/T	0.00438332	0.0466095	intron-variant	RNF126	GRCh38.p7	19:655368	CAACGCAACTAAAAA[C/T]GGGCAAAGTCGGGAG	55658
rs190126798	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:654619	TTGCACTGCAGCCTG[A/G]GCGAGGGAGCAAGAC	55658
rs190169148	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:658998	GGCAGCCGACATCCA[C/T]AGGTTCCCGGGGTAT	55658
rs190473107	snp	C/T	0.0119994	0.0765226	missense	RNF126	GRCh38.p7	19:648401	GCACGATGCAGCCGT[C/T]GTGGAACAGGTGGTT	55658
rs190692446	snp	A/G	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:660161	TCAGGACACCCTCAC[A/G]AGTCACCAGGAGAGC	55658
rs190728522	snp	A/T	0.00318978	0.0398085	upstream-variant-2KB	RNF126	GRCh38.p7	19:664076	GAGACGGAGTCTCAC[A/T]CTGTCACCCAGGCTG	55658
rs190938917	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:652353	CCCCCATGCGCCAGG[C/T]GCTCCCTCCCCTCAA	55658
rs191209188	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:654874	CAGGAGGCTGAGACA[A/G]GAGAATCGCTTGAAC	55658
rs191220679	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652527	CTCCTAAGCGTGAGA[A/G]TGTGGGTAGGGCCCC	55658
rs191360699	snp	A/G	0.00517822	0.0506191	intron-variant	RNF126	GRCh38.p7	19:648816	TCTACTGAAAATACA[A/G]GTATGAGCCAGGCGT	55658
rs191650250	snp	C/T	0.0158469	0.0875917	intron-variant	RNF126	GRCh38.p7	19:652174	GTGGGGACAGGCTGG[C/T]GCTCGGGGCCCCGAG	55658
rs191654464	snp	C/T	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:657556	GGGGCCTGTGCACGT[C/T]GGCCCTGCTGCTGGA	55658
rs191791161	snp	C/T	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:661921	GCTCTGCCACTTTCC[C/T]GCTGAGCCACCACGC	55658
rs191863871	snp	C/T	0.00517822	0.0506191	intron-variant	RNF126	GRCh38.p7	19:660734	TCCCAGGCTCAAGCG[C/T]TCCTCCCACCACCTC	55658
rs192024507	snp	A/G	0.0322114	0.122752	intron-variant	RNF126	GRCh38.p7	19:650122	GCTGGGGATGGGGAC[A/G]GGCACCCCCTCCTAC	55658
rs192291082	snp	C/T	0.0358015	0.128915	utr-variant-5-prime	RNF126	GRCh38.p7	19:663131	GGCCATGGCCGCCGC[C/T]ACCTACTCCGCGCCG	55658
rs192320430	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF126	GRCh38.p7	19:664887	CTCAGGTGATCCGCC[C/T]GCCTCGGCCTGCCAT	55658
rs192386591	snp	G/T	0.00318978	0.0398085	intron-variant	RNF126	GRCh38.p7	19:653318	TCCCCTGGCTCGGGG[G/T]AGGCCACGTCCACGC	55658
rs192548050	snp	A/G	0.00358779	0.0422022	intron-variant	RNF126	GRCh38.p7	19:655955	AGAAGACCACGCAGC[A/G]TGTGATCCCACGTCT	55658
rs192717356	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653807	CAAGTGCTCCATCGC[A/G]GCAACGTGAAAATGG	55658
rs192779561	snp	A/G	0.00318978	0.0398085	intron-variant	RNF126	GRCh38.p7	19:656661	AGAAAAAGAAAAAGA[A/G]AAAGGGAAAGGGGAA	55658
rs192852496	snp	C/T	0.00159617	0.0282053	intron-variant	RNF126	GRCh38.p7	19:651484	GCTGGAGGGCCTGGC[C/T]GGGCGGCCTCTCCAG	55658
rs192965845	snp	C/T	0.00358779	0.0422022	utr-variant-3-prime	RNF126	GRCh38.p7	19:647645	CCTCATGGTCCCGAG[C/T]CCCCCTACTCCGGGT	55658
rs193098616	snp	C/T	0.00261939	0.0360948	synonymous-codon	RNF126	GRCh38.p7	19:651826	CTGTCCGTAGCCCTG[C/T]GGCAGCGTGAACAGG	55658
rs193196086	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:653165	GCGCCTTGGCTGAGC[C/T]CCTCCGACCTGCCCC	55658
rs199592285	snp	C/T	0.00152334	0.0275563	intron-variant	RNF126	GRCh38.p7	19:652186	TGGCGCTCGGGGCCC[C/T]GAGCAAGGCTGACAC	55658
rs199596659	snp	C/T	0.000400153	0.0141392	intron-variant	RNF126	GRCh38.p7	19:648861	GTAATTCCCACTACT[C/T]GGGAGGCTGAGCTCT	55658
rs199674967	snp	C/T	0.000210522	0.0102575	synonymous-codon	RNF126	GRCh38.p7	19:648242	GGCCGTGTTCTGTCC[C/T]GTGAGGCTTTTTCGG	55658
rs199707341	snp	A/G			downstream-variant-500B	RNF126	GRCh38.p7	19:647274	GGGCAGAGGCGCTGG[A/G]CCCTGGCGCTTTAAC	55658
rs199754907	snp	C/T	0.000713351	0.0188724	intron-variant	RNF126	GRCh38.p7	19:651907	GGCCCGTGCAGTCTG[C/T]TGGGGGCGCTAGGGC	55658
rs199880261	snp	A/C/G	4.34245e-05	0.00465944	missense	RNF126	GRCh38.p7	19:652264	CTCTGGTCTGTGGGA[A/C/G]CTGTGGAGGGGGCAG	55658
rs199907468	snp	A/G	0.00215459	0.0327514	intron-variant	RNF126	GRCh38.p7	19:649020	GCTCCTCGGGGGCCC[A/G]GCCCGGGGCTCTGAA	55658
rs199971166	snp	A/C/G	0.000127445	0.00798163	intron-variant	RNF126	GRCh38.p7	19:648325	GGGCAGGTTAGAGGC[A/C/G]GGAGGGCCGCGGTCG	55658
rs199988837	in-del	-/ACCCCAACA	0.0023933	0.0345097	intron-variant	RNF126	GRCh38.p7	19:652500	GATAAACCGGTGCAG[-/ACCCCAACA]ACCCCAACAGCCTCC	55658
rs200240968	snp	C/T	0.00036901	0.0135783	intron-variant	RNF126	GRCh38.p7	19:651882	AGGGGGGCGTGACCT[C/T]GGGGGCTCAGGCCCG	55658
rs200294886	snp	C/T	8.87272e-05	0.00666001	intron-variant	RNF126	GRCh38.p7	19:648834	ATGAGCCAGGCGTGG[C/T]GGCGGGTGCCTGTAA	55658
rs200458687	snp	A/G	0.000228558	0.0106877	intron-variant	RNF126	GRCh38.p7	19:650303	TGGATGATCCTGGAA[A/G]AGAGAGCGCCAGTCA	55658
rs200494113	snp	A/G	7.33972e-05	0.00605749	synonymous-codon	RNF126	GRCh38.p7	19:651742	CTCAGGGTCCCTGCC[A/G]TCGTCAGCCTGCGCC	55658
rs200508004	snp	C/G/T	0.000605949	0.0173962	synonymous-codon	RNF126	GRCh38.p7	19:648176	CGAGCTGGAGGAGGA[C/G/T]GATGACGACGAGGAG	55658
rs200607809	snp	A/G	0.000391926	0.0139932	intron-variant	RNF126	GRCh38.p7	19:652923	GGTCACGGTGACGCC[A/G]GCATCACCTGCAAAC	55658
rs200639955	snp	C/T	0.00025393	0.011265	missense	RNF126	GRCh38.p7	19:648906	CCTCAGTGACGGGGA[C/T]GGTGGGGAGGGCCTG	55658
rs200861655	snp	C/T	0.000467399	0.0152801	intron-variant	RNF126	GRCh38.p7	19:648313	GGACGGGAGAAGGGG[C/T]AGGTTAGAGGCGGGA	55658
rs200892192	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:648856	TGCCTGTAATTCCCA[C/G]TACTCGGGAGGCTGA	55658
rs201030575	snp	C/G	0.000399281	0.0141238	synonymous-codon	RNF126	GRCh38.p7	19:649739	CATAGGGTTTGAGTG[C/G]AGGACTCCCCTGGAG	55658
rs201060989	snp	A/C	0.000602987	0.0173531	intron-variant	RNF126	GRCh38.p7	19:652820	TTCAACAGGGGGCTG[A/C]ATTACCTGGTCTCTT	55658
rs201121285	snp	A/C/T	0.00046901	0.0153072	missense	RNF126	GRCh38.p7	19:652246	ACCTCCAACGGTGGC[A/C/T]GGCTCTGGTCTGTGG	55658
rs201195440	in-del	-/T			intron-variant	RNF126	GRCh38.p7	19:655501	AAAAAAAAAGAAAAG[-/T]GGGGGGGGAAAGGAC	55658
rs201215740	snp	A/G	0.000937837	0.0216342	intron-variant	RNF126	GRCh38.p7	19:652914	AGGAGGCCGGGTCAC[A/G]GTGACGCCGGCATCA	55658
rs201289764	snp	C/T	6.16846e-05	0.00555324	missense	RNF126	GRCh38.p7	19:648476	TGCACACAGGGCACT[C/T]GAGCCCGGAGCCTGC	55658
rs201382085	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:650642	TTGTTGCCCAGGCTG[A/G]AGTGCAATGGCACGA	55658
rs201384051	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:648854	GGTGCCTGTAATTCC[C/T]ACTACTCGGGAGGCT	55658
rs201543493	snp	A/G	4.26739e-05	0.004619	missense	RNF126	GRCh38.p7	19:651723	GGTCTCTCTCCCGCC[A/G]GCTCTCAGGGTCCCT	55658
rs201553675	snp	A/C/T	0.000419203	0.0144717	intron-variant	RNF126	GRCh38.p7	19:651896	TCGGGGGCTCAGGCC[A/C/T]GTGCAGTCTGCTGGG	55658
rs201613651	in-del	-/CTA	0.0228947	0.104514	intron-variant	RNF126	GRCh38.p7	19:658501	GAGCCCCCGTGCTGG[-/CTA]CTGTTTTCCTAAAGG	55658
rs201714687	snp	A/G	0.000741152	0.0192361	intron-variant	RNF126	GRCh38.p7	19:648353	TCGGGGTGGGGGGGC[A/G]GGTGGGCGGGGCACT	55658
rs201723696	snp	A/C/T	0.000100558	0.00709006	intron-variant	RNF126	GRCh38.p7	19:648301	GGACAGAGGCAGGGA[A/C/T]GGGAGAAGGGGCAGG	55658
rs201744899	snp	C/T	0.000583911	0.0170767	missense	RNF126	GRCh38.p7	19:650280	TGATGATGCCGTTGA[C/T]GAGCTGCTGGATGAT	55658
rs201838516	snp	A/G	0.000874427	0.0208914	intron-variant	RNF126	GRCh38.p7	19:652223	GAAGCACGAGGGGCG[A/G]GCGACTCACCTCCAA	55658
rs201880227	snp	A/C			intron-variant	RNF126	GRCh38.p7	19:661340	AGGGGCTGCAAGGGG[A/C]TGCCCTGCAACTCAC	55658
rs201919796	in-del	-/CCGC	0.00597604	0.0543351	intron-variant	RNF126	GRCh38.p7	19:656911	AGGGGTTGCCGCCGT[-/CCGC]CCGCCCGCCAGCTGA	55658
rs201983768	snp	C/T	0.000343997	0.0131103	synonymous-codon	RNF126	GRCh38.p7	19:651769	CGCCCCAGGAGGGAA[C/T]GTGGGGATCTCGAAG	55658
rs201992927	snp	A/G	9.10871e-05	0.00674798	intron-variant	RNF126	GRCh38.p7	19:649664	CAGGCACTCTGGGCC[A/G]TGGCCACGCTGTACC	55658
rs202052869	snp	C/T	0.000216802	0.0104093	intron-variant	RNF126	GRCh38.p7	19:650330	GTCACGGGGTGAGGC[C/T]GCCCCACGCACAGGA	55658
rs202056846	in-del	-/C			intron-variant	RNF126	GRCh38.p7	19:649106	GCCCCTTGGAGCCCG[-/C]CCCGGGGTCGGAGAT	55658
rs202090513	snp	A/G	0.000252483	0.0112329	intron-variant	RNF126	GRCh38.p7	19:648838	GCCAGGCGTGGCGGC[A/G]GGTGCCTGTAATTCC	55658
rs202094517	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:652786	CAACAGCTGAGGCCC[A/G]GCTGGCTCTTCCAGC	55658
rs367593189	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:652510	GTGCAGACCCCAACA[A/G]CCTCCTAAGCGTGAG	55658
rs367870751	snp	A/G	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:653940	TGGGGGAGTGCTGTG[A/G]GGGGAGCCAAGGTCG	55658
rs367959759	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:661247	AGCTAAATGTGCAGC[C/T]GAGTCAAGGCAGTGT	55658
rs367985115	snp	A/G	0.000244608	0.0110564	intron-variant	RNF126	GRCh38.p7	19:648840	CAGGCGTGGCGGCGG[A/G]TGCCTGTAATTCCCA	55658
rs368068806	snp	A/C	0.000157987	0.00888643	intron-variant	RNF126	GRCh38.p7	19:650339	TGAGGCCGCCCCACG[A/C]ACAGGAGAGGCGCCA	55658
rs368100858	snp	A/G	0.000165336	0.00909068	utr-variant-3-prime	RNF126	GRCh38.p7	19:648112	GCCCCGTGCTTTCCC[A/G]ACGGCCGACGTGGGC	55658
rs368110127	snp	A/C			intron-variant	RNF126	GRCh38.p7	19:657156	GCAGCCCCAGAAGGG[A/C]CTGAGGGAGAAGCTG	55658
rs368133350	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:652596	GCCGCCGAGGCTGAG[A/G]GAGGTGAGCGGCTGC	55658
rs368141828	snp	C/T			utr-variant-3-prime	RNF126	GRCh38.p7	19:648099	GTGGGTGGGAAAGGC[C/T]CCGTGCTTTCCCGAC	55658
rs368185772	snp	C/T	0.000659495	0.018147	missense, intron-variant	RNF126	GRCh38.p7	19:651687	GGGGCTGTCGGGCGC[C/T]GTACCGGTGCCGGGA	55658
rs368203345	snp	A/G	0.000804009	0.0200339	synonymous-codon	RNF126	GRCh38.p7	19:652864	GATAAAACCAGACTC[A/G]CATCTTGGACAGATA	55658
rs368239447	snp	A/G	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:660537	GAGACGCCCCGTTTC[A/G]AGGGCACTGGTTGTG	55658
rs368272407	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:650685	GCAACCTCTGCCTCC[C/T]GGGTTCAAGTGATTC	55658
rs368332176	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:658313	GGGCCCAGGGCCAGG[C/T]GCATGGAGGGGAGTG	55658
rs368620647	snp	A/C/T	0.000330992	0.0128608	synonymous-codon, intron-variant	RNF126	GRCh38.p7	19:651619	CCCTCACCCTTCCAG[A/C/T]GTGGGGACGCCTTCG	55658
rs368767739	snp	A/C/G			intron-variant	RNF126	GRCh38.p7	19:661708	GGGTCTCTACTCCCG[A/C/G]GGAACTGCACTGCTT	55658
rs368836566	snp	C/T	0.000369549	0.0135882	intron-variant	RNF126	GRCh38.p7	19:652214	CACGATCGGGAAGCA[C/T]GAGGGGCGGGCGACT	55658
rs368907748	snp	A/G	5.54093e-05	0.00526323	synonymous-codon	RNF126	GRCh38.p7	19:650248	CCAGGGGCCCAGGCT[A/G]GGGATGGTGGCGGGC	55658
rs368909706	snp	A/G	0.000149903	0.00865614	synonymous-codon	RNF126	GRCh38.p7	19:649718	GTTGGCCCCCCAGGC[A/G]TAGTCCATAGGGTTT	55658
rs369194380	snp	A/G	0.000157988	0.00888645	intron-variant	RNF126	GRCh38.p7	19:650210	CCAGGCTGGGGATGG[A/G]GACAGGCACCCCCAC	55658
rs369528281	snp	A/G	0.00478085	0.0486577	intron-variant	RNF126	GRCh38.p7	19:656104	CTGTGAGAATGCTGT[A/G]GAATTAGACTGTGGT	55658
rs369565076	snp	A/G	0.000727709	0.0190611	intron-variant	RNF126	GRCh38.p7	19:652907	AGAGAACAGGAGGCC[A/G]GGTCACGGTGACGCC	55658
rs369610129	snp	A/G	0.000170198	0.00922335	missense	RNF126	GRCh38.p7	19:652247	CCTCCAACGGTGGCC[A/G]GCTCTGGTCTGTGGG	55658
rs369622203	in-del	-/AGGCCCG			intron-variant	RNF126	GRCh38.p7	19:652786	AACAGCTGAGGCCCG[-/AGGCCCG]GCTGGCTCTTCCAGC	55658
rs369651109	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:649524	GGCAGGAGGAAGGCC[A/G]GAGCTGCCCCCTGTG	55658
rs369924439	in-del	-/GTTT			upstream-variant-2KB	RNF126	GRCh38.p7	19:664652	TTTGTTTGTTTGTTT[-/GTTT]TTTAGAGATGGAGTC	55658
rs370023734	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RNF126	GRCh38.p7	19:664155	GTTCAAGCGATTCTC[C/T]CGCCTCAGCCTCTCG	55658
rs370024198	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:654329	TGCGTTTCAGCCCAC[A/G]CCCCACGAATTCTCG	55658
rs370130248	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:650351	ACGCACAGGAGAGGC[A/G]CCAGGCCTGCCAGGT	55658
rs370193144	snp	C/T	0.000378286	0.0137477	intron-variant	RNF126	GRCh38.p7	19:652325	GCAGGTCAGCAGTGC[C/T]GGCTACCCTGTGCCC	55658
rs370228102	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:655379	AAAACGGGCAAAGTC[A/G]GGAGGCTGAGGCAGG	55658
rs370275973	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:653753	GCAGAACTGGAAACT[C/G]GAAGCTAAATCAACT	55658
rs370334128	snp	C/G	0.00356052	0.0420426	intron-variant	RNF126	GRCh38.p7	19:651869	TGCTGGGGAGAGGAG[C/G]GGGGCGTGACCTCGG	55658
rs370350292	snp	A/G	0.00199481	0.0315187	utr-variant-3-prime	RNF126	GRCh38.p7	19:647825	TGAGCTCAAACGTCC[A/G]TTTATTTCAAAGCAG	55658
rs370358904	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:656943	CGGGAGCCCAGGGCC[A/G]CTCCATCGCCTGGGT	55658
rs370584191	snp	A/T	3.8975e-05	0.00441429	intron-variant	RNF126	GRCh38.p7	19:648851	GCGGGTGCCTGTAAT[A/T]CCCACTACTCGGGAG	55658
rs370588810	snp	A/G/T	3.69442e-05	0.00429779	intron-variant	RNF126	GRCh38.p7	19:652814	AGCCTCTTCAACAGG[A/G/T]GGCTGCATTACCTGG	55658
rs370610094	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:659944	AATCTTTTGTATTTT[C/T]AGTAGGGATGGGGTT	55658
rs370629184	snp	A/G	5.45837e-05	0.00522387	synonymous-codon	RNF126	GRCh38.p7	19:648886	AGCTCTCATACCTAC[A/G]TGCTCCTCAGTGACG	55658
rs370648660	snp	C/T			upstream-variant-2KB	RNF126	GRCh38.p7	19:665268	GGTTTTCCGTTGGCT[C/T]GGAGCAGACATGAGG	55658
rs370716676	snp	A/G	0.00021411	0.0103445	intron-variant	RNF126	GRCh38.p7	19:648835	TGAGCCAGGCGTGGC[A/G]GCGGGTGCCTGTAAT	55658
rs370737357	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:662838	CCCGCCCGGGCCTCA[A/G]TCTCCCGCATGTACA	55658
rs370772673	snp	C/T	0.000375982	0.0137058	intron-variant	RNF126	GRCh38.p7	19:650337	GGTGAGGCCGCCCCA[C/T]GCACAGGAGAGGCGC	55658
rs370835693	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:660540	ACGCCCCGTTTCGAG[A/G]GCACTGGTTGTGGCT	55658
rs370960082	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:652463	CGCTGCTGCTTCCCT[C/T]GCCAGTAAACCACGG	55658
rs371134337	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:656728	CTTAGTGTGGGAGCA[A/G]TGTGGCTCTGCCACA	55658
rs371174038	snp	A/G	0.000201238	0.0100289	synonymous-codon	RNF126	GRCh38.p7	19:648146	CGAGTTGCTTGTGGC[A/G]TTCTCGTTGCTGGGC	55658
rs371175732	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:656876	TGCCGGTGTCGGGTC[C/T]ATCGGGGCTCCTCTG	55658
rs371241189	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:661630	TGCCCCAACTCTAGC[A/G]CTCGCTCCTCCTCTG	55658
rs371360961	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	RNF126	GRCh38.p7	19:663397	GGCCAAAGCAGGCGG[C/T]GGAAGAGACGAGAAG	55658
rs371363227	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:660871	CTGCCATGCTGTCTA[C/T]GGGCGCCTTGTTGCG	55658
rs371379933	snp	C/G	0.000309952	0.0124451	intron-variant	RNF126	GRCh38.p7	19:652217	GATCGGGAAGCACGA[C/G]GGGCGGGCGACTCAC	55658
rs371414624	snp	C/T	0.000691589	0.0185827	intron-variant	RNF126	GRCh38.p7	19:652346	CCCTGTGCCCCCATG[C/T]GCCAGGCGCTCCCTC	55658
rs371454522	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:659324	GACACTGGCCGTAGC[A/G]GCCCTCACTTCCTGG	55658
rs371509659	snp	C/T	8.87062e-05	0.00665922	synonymous-codon	RNF126	GRCh38.p7	19:648940	TTTCTCTTTATCTGC[C/T]GGTGGGGGGCCTGTG	55658
rs371515609	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	RNF126	GRCh38.p7	19:663800	ATACAGGCAGACCCG[A/G]GGCTCAGGGCGCTGT	55658
rs371523615	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:653920	GACAAGGCTCCCACC[A/G]TGCATGGGGGAGTGC	55658
rs371608034	snp	C/G	0.000155988	0.00883004	intron-variant	RNF126	GRCh38.p7	19:650307	TGATCCTGGAAAAGA[C/G]AGCGCCAGTCACGGG	55658
rs371617069	snp	A/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:651389	CTGGCAGGCACACGG[A/T]GCCCCACTCTGTGGT	55658
rs371771354	in-del	-/GTTCAAGTG			intron-variant	RNF126	GRCh38.p7	19:650688	ACCTCTGCCTCCCGG[-/GTTCAAGTG]ATTCTCCTGCCTCAG	55658
rs371844525	snp	A/G	3.36865e-05	0.00410391	synonymous-codon	RNF126	GRCh38.p7	19:648955	CGGTGGGGGGCCTGT[A/G]TTTTCAAACTGATTG	55658
rs371871232	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:653954	GAGGGGAGCCAAGGT[C/T]GACCCCAGGCTCTGG	55658
rs372027724	snp	A/C			intron-variant	RNF126	GRCh38.p7	19:658198	GTGCCGGGCTCCACC[A/C]ATGCACCCCTGCAGC	55658
rs372094976	snp	C/T	0.000325468	0.0127526	intron-variant	RNF126	GRCh38.p7	19:648507	GGGAGTGTGCAGCTG[C/T]GGTCACAGCGGGCGT	55658
rs372154325	snp	A/G	8.46991e-05	0.0065071	intron-variant	RNF126	GRCh38.p7	19:648284	GCTGTCGTGCTTTGT[A/G]GGGACAGAGGCAGGG	55658
rs372270839	snp	A/G	0.000379348	0.013767	intron-variant	RNF126	GRCh38.p7	19:652187	GGCGCTCGGGGCCCC[A/G]AGCAAGGCTGACACG	55658
rs372324827	snp	A/G/T	3.77154e-05	0.00434241	intron-variant	RNF126	GRCh38.p7	19:651891	TGACCTCGGGGGCTC[A/G/T]GGCCCGTGCAGTCTG	55658
rs372430655	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:655440	GCAGTGAGCCGAGAT[C/T]GCGCCACTGCACTCT	55658
rs372448035	snp	C/T	0.000307952	0.0124049	missense	RNF126	GRCh38.p7	19:651695	CGGGCGCCGTACCGG[C/T]GCCGGGACGGATGGT	55658
rs372482320	snp	C/T	0.00119737	0.0244387	downstream-variant-500B	RNF126	GRCh38.p7	19:647059	CCATCGTCTGATTCT[C/T]GGATCCCAGGATGGT	55658
rs372566197	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:654915	GAGGCTGCAACGAGC[C/T]GAGATCATGACATTG	55658
rs372711344	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:649917	ACCCACTCACCAGGG[A/G]CCCAGGCTGGGGATG	55658
rs372731683	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:655730	AAGACACCTGCCCAC[C/G]AAATGTTCACATGGC	55658
rs372875254	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:653508	AAGCCACAGCTGTGC[C/T]GAGCAGGACGGATGC	55658
rs372973894	snp	C/T	0.0011035	0.0234634	missense, intron-variant	RNF126	GRCh38.p7	19:651642	CGCCTTCGTGCCGGC[C/T]GGTGGCCCGCCGCGT	55658
rs372979815	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652550	AGGGCCCCCGTGGCC[C/T]CTTCCCCGGAGGGCC	55658
rs373019907	in-del	-/A			intron-variant	RNF126	GRCh38.p7	19:654208	CCAGGGTGAGCAAAC[-/A]GATGCCAGATGCACA	55658
rs373105271	snp	C/T	0.000374271	0.0136746	missense	RNF126	GRCh38.p7	19:651792	TCTCGAAGCTGTCAT[C/T]GAAGATGCCGAAAGC	55658
rs373118509	snp	C/T	0.000260349	0.0114064	intron-variant	RNF126	GRCh38.p7	19:650319	AGAGAGCGCCAGTCA[C/T]GGGGTGAGGCCGCCC	55658
rs373201260	snp	A/G	0.000155988	0.00883004	missense	RNF126	GRCh38.p7	19:648448	ACACGCTCACCCAGC[A/G]CGTAGTCGTCCTTGC	55658
rs373219354	snp	A/G	0.000358404	0.0133818	intron-variant	RNF126	GRCh38.p7	19:652920	CCGGGTCACGGTGAC[A/G]CCGGCATCACCTGCA	55658
rs373244930	snp	A/G	0.000664525	0.018216	synonymous-codon	RNF126	GRCh38.p7	19:652275	GGGAGCTGTGGAGGG[A/G]GCAGAACCATTTTCT	55658
rs373253384	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:656594	CAGAGGTTGCAGTGA[C/G]CCGAGATCATACCAC	55658
rs373285669	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:659746	TTGCTGCTCAGACAC[C/T]CAGACACCCTCGTCA	55658
rs373304214	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:662519	GCCTCCAAGGCGGCG[A/G]CCAGGGCTCCACGAG	55658
rs373453080	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:662179	TTAGAAATGCAGACT[A/G]CTGAGCGCATTCCAC	55658
rs373501267	snp	A/C	7.24979e-05	0.00602027	intron-variant	RNF126	GRCh38.p7	19:650213	GGCTGGGGATGGGGA[A/C]AGGCACCCCCACCCA	55658
rs373686703	snp	C/T	0.000161799	0.00899297	intron-variant	RNF126	GRCh38.p7	19:648324	GGGGCAGGTTAGAGG[C/T]GGGAGGGCCGCGGTC	55658
rs373917496	snp	A/G	7.63854e-05	0.00617955	intron-variant	RNF126	GRCh38.p7	19:650338	GTGAGGCCGCCCCAC[A/G]CACAGGAGAGGCGCC	55658
rs373918948	snp	C/T	0.000101019	0.00710627	utr-variant-3-prime	RNF126	GRCh38.p7	19:648111	GGCCCCGTGCTTTCC[C/T]GACGGCCGACGTGGG	55658
rs373942388	snp	A/C			intron-variant	RNF126	GRCh38.p7	19:657059	GAACAGCTGCACTGG[A/C]CCCCACTGAGGGCAG	55658
rs373953236	snp	C/T	0.000204985	0.0101218	intron-variant	RNF126	GRCh38.p7	19:651914	GCAGTCTGCTGGGGG[C/T]GCTAGGGCACAAAGA	55658
rs374000460	snp	A/G	0.0023933	0.0345097	intron-variant	RNF126	GRCh38.p7	19:659954	ATTTTTAGTAGGGAT[A/G]GGGTTTTACCATGTT	55658
rs374151896	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:661705	CCTGGGTCTCTACTC[C/T]CGGGGAACTGCACTG	55658
rs374272881	snp	A/G	0.000157988	0.00888645	intron-variant	RNF126	GRCh38.p7	19:652347	CCTGTGCCCCCATGC[A/G]CCAGGCGCTCCCTCC	55658
rs374339848	snp	A/G	0.000299783	0.0122393	synonymous-codon	RNF126	GRCh38.p7	19:649730	GGCGTAGTCCATAGG[A/G]TTTGAGTGCAGGACT	55658
rs374348740	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:659397	GCAGGGCCCAGCACC[C/T]CCACCGTCCTCTCAC	55658
rs374400339	snp	C/T			synonymous-codon	RNF126	GRCh38.p7	19:648149	GTTGCTTGTGGCGTT[C/T]TCGTTGCTGGGCGAG	55658
rs374476341	snp	A/G	0.00318978	0.0398085	intron-variant	RNF126	GRCh38.p7	19:656730	TAGTGTGGGAGCAGT[A/G]TGGCTCTGCCACAGT	55658
rs374476503	snp	C/G			downstream-variant-500B	RNF126	GRCh38.p7	19:647522	GGAAAGCCACAGCAC[C/G]GGCTTCTCTTTGTAA	55658
rs374502782	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:651187	TCTGTTCCACCAGGA[A/G]TGGGGCCCTGCGACG	55658
rs374532719	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:653671	GGGCCTGGGCTGAAA[C/T]GTGCATGGTGCCTCC	55658
rs374661801	snp	C/T	0.00159617	0.0282053	intron-variant	RNF126	GRCh38.p7	19:655603	CAGGGCCAGCCAGGA[C/T]GAGATGCAAGACCCC	55658
rs374663177	snp	C/G			upstream-variant-2KB	RNF126	GRCh38.p7	19:663431	GGCGTGCGCGGGGCG[C/G]GGCCGAGGCCCTCCT	55658
rs374773860	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:650432	TATTTATTTATTTTA[C/T]TATGAGCCAGGGTCT	55658
rs374820130	snp	A/C/T	0.000127059	0.0079697	missense	RNF126	GRCh38.p7	19:648145	ACGAGTTGCTTGTGG[A/C/T]GTTCTCGTTGCTGGG	55658
rs374963832	snp	A/G	0.0010838	0.0232535	intron-variant	RNF126	GRCh38.p7	19:652326	CAGGTCAGCAGTGCC[A/G]GCTACCCTGTGCCCC	55658
rs375079150	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:651386	GGCCTGGCAGGCACA[C/T]GGTGCCCCACTCTGT	55658
rs375194374	snp	C/T	0.000535173	0.0163493	synonymous-codon	RNF126	GRCh38.p7	19:651703	GTACCGGTGCCGGGA[C/T]GGATGGTCTCTCTCC	55658
rs375335521	snp	C/T	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:654043	CAGCAAGCAAGATCC[C/T]GGCCTCACCCACTGA	55658
rs375340680	snp	A/C/G	0.000229328	0.010706	intron-variant	RNF126	GRCh38.p7	19:651897	CGGGGGCTCAGGCCC[A/C/G]TGCAGTCTGCTGGGG	55658
rs375360361	snp	A/G	8.77894e-05	0.00662473	missense	RNF126	GRCh38.p7	19:651755	CCGTCGTCAGCCTGC[A/G]CCCCAGGAGGGAACG	55658
rs375494893	snp	C/T	0.00651459	0.0566997	intron-variant	RNF126	GRCh38.p7	19:648520	TGCGGTCACAGCGGG[C/T]GTGGGGGGCCTGCCG	55658
rs375587331	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:652496	TTCTCGATAAACCGG[C/T]GCAGACCCCAACAGC	55658
rs375701327	snp	C/T	0.000373984	0.0136694	missense	RNF126	GRCh38.p7	19:651801	TGTCATCGAAGATGC[C/T]GAAAGCAAACTGTCC	55658
rs375725150	snp	C/T	0.00676609	0.0577691	intron-variant	RNF126	GRCh38.p7	19:660880	TGTCTACGGGCGCCT[C/T]GTTGCGTCCTGCTCC	55658
rs375952048	snp	C/T			upstream-variant-2KB	RNF126	GRCh38.p7	19:665312	CCTCAGCCCTCTCTG[C/T]GCTCTGCTGCCTGCC	55658
rs375963612	snp	A/G	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:653111	GATCTGAGCCCCTCC[A/G]ACCTGGCCCCACCGT	55658
rs376002128	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:655461	ACTGCACTCTAGCCC[A/G]GGCGACAGAGTGACA	55658
rs376030251	snp	A/G	0.00398564	0.0444627	intron-variant	RNF126	GRCh38.p7	19:652035	GGTGTGAGATGCCTC[A/G]GTGGAAGTTTCGCTT	55658
rs376048427	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:662677	TCTCTCTGCTCGCCG[A/G]GCCTCAGTTTCTCCG	55658
rs376111036	snp	A/G/T	0.00260463	0.0360067	intron-variant	RNF126	GRCh38.p7	19:650320	GAGAGCGCCAGTCAC[A/G/T]GGGTGAGGCCGCCCC	55658
rs376151423	snp	A/G	0.000159593	0.00893146	synonymous-codon	RNF126	GRCh38.p7	19:652849	TTCCGGAAGCTCCTC[A/G]ATAAAACCAGACTCG	55658
rs376157639	snp	A/G	7.62747e-05	0.00617508	synonymous-codon	RNF126	GRCh38.p7	19:648907	CTCAGTGACGGGGAC[A/G]GTGGGGAGGGCCTGG	55658
rs376174636	snp	C/T			utr-variant-3-prime	RNF126	GRCh38.p7	19:647922	CGGGGAGGCTGGGGA[C/T]GCCCCAGAGGGGACC	55658
rs376245439	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:655878	GCCCAGACCAGGCCA[C/T]GGCGGGGGGGAGGGG	55658
rs376304140	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:659314	CCCCATCAGTGACAC[C/T]GGCCGTAGCAGCCCT	55658
rs376364796	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:660205	CCACTCTGCACACAC[A/G]TGCCCACCAGATGCC	55658
rs376419272	snp	G/T	0.00159617	0.0282053	intron-variant	RNF126	GRCh38.p7	19:652455	CCGTAACCCGCTGCT[G/T]CTTCCCTCGCCAGTA	55658
rs376556991	snp	C/T	0.000162149	0.00900268	intron-variant	RNF126	GRCh38.p7	19:652311	CCTGGGGAGAGAGTG[C/T]AGGTCAGCAGTGCCG	55658
rs376680366	snp	A/C			intron-variant	RNF126	GRCh38.p7	19:653527	CAGGACGGATGCCAT[A/C]CCCTGTGGATCTCAC	55658
rs376774165	snp	A/G	0.00398564	0.0444627	intron-variant	RNF126	GRCh38.p7	19:658940	AGGAAATTCAGCACC[A/G]GCATCTGCCCGAGGC	55658
rs376774192	snp	C/T	0.000163082	0.00902854	intron-variant	RNF126	GRCh38.p7	19:652913	CAGGAGGCCGGGTCA[C/T]GGTGACGCCGGCATC	55658
rs376778263	snp	C/T	0.00152014	0.0275274	intron-variant	RNF126	GRCh38.p7	19:648335	GAGGCGGGAGGGCCG[C/T]GGTCGGGGTGGGGGG	55658
rs376781342	snp	C/G/T	5.72681e-05	0.00535082	intron-variant	RNF126	GRCh38.p7	19:652898	TCCTGCAGGAGAGAA[C/G/T]AGGAGGCCGGGTCAC	55658
rs376866890	snp	A/G	1.79126e-05	0.00299266	intron-variant	RNF126	GRCh38.p7	19:651868	GTGCTGGGGAGAGGA[A/G]GGGGGCGTGACCTCG	55658
rs376871619	snp	A/G	7.18726e-05	0.00599426	intron-variant	RNF126	GRCh38.p7	19:650214	GCTGGGGATGGGGAC[A/G]GGCACCCCCACCCAC	55658
rs376880970	snp	A/C/T			intron-variant	RNF126	GRCh38.p7	19:651535	CGTTTCCGTGGAACC[A/C/T]GTGCTGGATTCTAAG	55658
rs376912354	in-del	-/GAA			intron-variant	RNF126	GRCh38.p7	19:655014	AAAGAAAGAAAGAAA[-/GAA]AAAAAAGCCCAGGCC	55658
rs376966401	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:649433	CATGTGACTGTGGGC[A/G]AGTCCTCCCCGCGGT	55658
rs376986346	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RNF126	GRCh38.p7	19:664357	CTCATGCGTGTATTT[A/C]TTTCTTCACTCAACA	55658
rs377143537	snp	C/T	0.000381025	0.0137974	intron-variant	RNF126	GRCh38.p7	19:649800	CAGCTGGGGCAGGTG[C/T]GTCTATCCACCCCAC	55658
rs377157607	snp	A/G/T			intron-variant	RNF126	GRCh38.p7	19:650105	ACTCACCAGGGGCCC[A/G/T]GGCTGGGGATGGGGA	55658
rs377199240	in-del	-/GT			intron-variant	RNF126	GRCh38.p7	19:656051	GGGAGGGGACGGGGA[-/GT]GACGGCTGGCAGGGC	55658
rs377410742	snp	A/C	4.58495e-05	0.00478776	intron-variant	RNF126	GRCh38.p7	19:652227	CACGAGGGGCGGGCG[A/C]CTCACCTCCAACGGT	55658
rs377717043	snp	C/T	7.34349e-05	0.00605905	intron-variant	RNF126	GRCh38.p7	19:652342	GCTACCCTGTGCCCC[C/T]ATGCGCCAGGCGCTC	55658
rs377729643	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:660837	ACAGGGTCCTGCCAC[A/G]TACGGAGAAGTTCTG	55658
rs377756864	snp	A/G	0.00199481	0.0315187	intron-variant	RNF126	GRCh38.p7	19:659504	GAACCACCCAGAGAC[A/G]GGGAGGTCAGGGGCA	55658
rs386388336	in-del	-/TT			intron-variant	RNF126	GRCh38.p7	19:650608	TTTTTTTTTTTTTTT[-/TT]TGAGACAGAGTTTCA	55658
rs386805657	in-del	GG/T			intron-variant	RNF126	GRCh38.p7	19:648350	CGGTCGGGGTGGGGG[GG/T]CGGGTGGGCGGGGCA	55658
rs386805658	in-del	AA/GAG			intron-variant	RNF126	GRCh38.p7	19:656251	GCTGCTAGGGAGGCT[AA/GAG]GTGCCAGGATCGCTT	55658
rs386805659	multinucleotide-polymorphism	CA/TG			intron-variant	RNF126	GRCh38.p7	19:656701	GCCAACGACCACCAC[CA/TG]TGGCCCTGAGCTTAG	55658
rs397732069	in-del	-/GA	0	0	upstream-variant-2KB	RNF126	GRCh38.p7	19:664594	GAGGCATTGGAGCGA[-/GA]CTGTTGAGGAATTAA	55658
rs397762739	in-del	-/G			intron-variant	RNF126	GRCh38.p7	19:658371	TGACAGTGACCAGGG[-/G]CAGGCAGGCCCCTGG	55658
rs527503491	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:656294	GGTGGAGGCTGCAGT[A/G]AGCCAAGATTGCAGC	55658
rs527505708	snp	A/G	0.00517822	0.0506191	intron-variant	RNF126	GRCh38.p7	19:661264	AGTCAAGGCAGTGTC[A/G]GCCCCCCACAGCCAC	55658
rs527621204	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:656750	TCTGCCACAGTGGCC[A/G]TGACAACTCTCCCCA	55658
rs527623228	snp	A/C			upstream-variant-2KB	RNF126	GRCh38.p7	19:665036	CCAGTCATTCCTGCT[A/C]TGACCACCAGAGAGC	55658
rs527823171	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:655158	CTACAAAAAACAAAT[C/T]AGCTGGGTATGCTGG	55658
rs527890928	snp	C/T	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:652393	TTGGGAGAGCAGGAA[C/T]TGTCCTTGGCACTGC	55658
rs527960848	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:649257	GAGTGCCCTGACGGC[A/G]GAATGGGGGGGCCGT	55658
rs528088221	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:654003	GGCTGTTCAGTCTTC[A/G]CAGGGGCAGGGGCTG	55658
rs528146502	snp	C/T	0.000208431	0.0102065	missense	RNF126	GRCh38.p7	19:648436	GGCAGCTGCCGCACA[C/T]GCTCACCCAGCGCGT	55658
rs528261242	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:648603	CCAGCGAGGGGAGAA[A/C]AGCCGTGTGTGTGTC	55658
rs528483390	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:651442	CATACTTCTGTCTCC[A/G]AAGGGCCGTGTGGGG	55658
rs528487167	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF126	GRCh38.p7	19:647649	ATGGTCCCGAGCCCC[C/T]CTACTCCGGGTCGTG	55658
rs528499741	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF126	GRCh38.p7	19:648010	TGGAACAGGCGGGAC[C/T]TGCAGCGCTGACCAG	55658
rs528658455	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:662950	TCGTGGTCAGCTCGC[C/G]CAAGAGGCGGGCGCA	55658
rs528724441	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:653236	CAGGTGGCACCACTC[A/G]GAGGGGTGCCCCAAT	55658
rs528819766	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:661482	TCAGTCTCAGCTCCC[C/G]AACCTTCGCCCCACA	55658
rs529101578	snp	A/G	0.00159617	0.0282053	intron-variant	RNF126	GRCh38.p7	19:653290	CGCTCTGGCAGCCCC[A/G]CACACAGCCCGTTCC	55658
rs529231030	in-del	-/G	0.00358779	0.0422022	intron-variant	RNF126	GRCh38.p7	19:653175	GAGCCCCTCCGACCT[-/G]GCCCCACCGTGACGG	55658
rs529231459	snp	C/T	0.00597247	0.0543191	intron-variant	RNF126	GRCh38.p7	19:651174	GGCTCCCCCAGGCTC[C/T]GTTCCACCAGGAATG	55658
rs529245507	snp	A/T			intron-variant	RNF126	GRCh38.p7	19:659989	AGGCTGGTCTCGAAC[A/T]CCTGACCTCAGGTGA	55658
rs529376158	snp	A/C	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:649924	CACCAGGGGCCCAGG[A/C]TGGGGATGGGAACAG	55658
rs529511676	snp	A/G	0.00199481	0.0315187	downstream-variant-500B	RNF126	GRCh38.p7	19:647154	TTGCCAGCTGTGCCC[A/G]AGCTGGCTGCACCCC	55658
rs529701253	snp	G/T	3.08732e-05	0.00392883	synonymous-codon	RNF126	GRCh38.p7	19:648946	TTTATCTGCCGGTGG[G/T]GGGCCTGTGTTTTCA	55658
rs529713487	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:649234	ATGGGGGGGGGGGCC[A/G]CGCTCCTGAGTGCCC	55658
rs529976448	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:660589	CAGATACGGAGCAGC[C/T]GTCCCTCCCCAGAAC	55658
rs529984887	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:660886	CGGGCGCCTTGTTGC[A/G]TCCTGCTCCAAAGGC	55658
rs530001995	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RNF126	GRCh38.p7	19:663699	GATTCCCTCCCGATG[C/T]ACTGTCAGGTCAGCT	55658
rs530044690	snp	A/C/G	0.00159649	0.0282165	intron-variant	RNF126	GRCh38.p7	19:655748	ATGTTCACATGGCCA[A/C/G]AACTGGCAGGTGAGA	55658
rs530112709	snp	C/T	0.0023933	0.0345097	upstream-variant-2KB	RNF126	GRCh38.p7	19:664204	CACCCGCCACCACAC[C/T]GGCTAATTTTTGTAT	55658
rs530186547	snp	G/T	0.00199481	0.0315187	intron-variant	RNF126	GRCh38.p7	19:659921	GGTGCCTGCCACCAC[G/T]CCTGGCCAATCTTTT	55658
rs530253392	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:659589	GCCCTCAGCAGCTCT[C/T]GCCCACACCCTACAG	55658
rs530265561	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:654371	CATCACCGGGGGCGC[A/G]GTGGCTCAGGCCTGT	55658
rs530549834	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:651527	TGATGCCACGTTTCC[A/G]TGGAACCCGTGCTGG	55658
rs530549904	snp	G/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653981	CTGGGGATGCAGGTT[G/T]CACCGGGGCTGTTCA	55658
rs530607552	snp	A/G	0.000191259	0.00977717	utr-variant-3-prime	RNF126	GRCh38.p7	19:648082	TGTGGCGCTGGCTGA[A/G]GGTGGGTGGGAAAGG	55658
rs530609859	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:651885	GGGGCGTGACCTCGG[A/G]GGCTCAGGCCCGTGC	55658
rs530802486	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:650775	TTTTTGTATTCTTAG[C/T]AGAGACGGAGTTTCA	55658
rs530812123	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	RNF126	GRCh38.p7	19:647256	AGGTGTGACCGAAGC[A/G]TGGGGCAGAGGCGCT	55658
rs530931858	snp	A/G	0.0209421	0.100162	intron-variant	RNF126	GRCh38.p7	19:651146	TGTTCCACCAGGAGC[A/G]GGGCCCAGCGACGGC	55658
rs530999119	snp	C/T	0.00318978	0.0398085	utr-variant-3-prime	RNF126	GRCh38.p7	19:647641	TCATCCTCATGGTCC[C/T]GAGCCCCCCTACTCC	55658
rs531020286	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:658289	GCCTGCACGGGGCGC[A/G]TGTCCTGAGGGCCCA	55658
rs531151234	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:657988	GGGGGCCTGGTGAAG[A/G]AGCTGCCCCACCTTC	55658
rs531347465	snp	A/G	0.00438332	0.0466095	intron-variant	RNF126	GRCh38.p7	19:661366	CTCACCCAGGCTGGC[A/G]GGCTGTCAGGCAACC	55658
rs531486171	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:656773	TCTCCCCAGGCGTCG[C/G]TTCTTGGGGTGTGTT	55658
rs531552550	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:657336	TTTCTGTCGGGCTCC[C/T]GGGTTCCCGTCTCAG	55658
rs531561821	snp	A/C	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:660517	GGGCAAGCTCCCCAG[A/C]GGCAGAGACGCCCCG	55658
rs531667148	snp	A/G	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:653044	TCCTGGAGGGCGGCC[A/G]AGGGGACCTGGCCTC	55658
rs531724615	snp	G/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:656043	GGGCCTGGGGGAGGG[G/T]ACGGGGAGTGACGGC	55658
rs531738727	in-del	-/A	0.00159617	0.0282053	intron-variant	RNF126	GRCh38.p7	19:656646	GAGTGAGACCGTGTC[-/A]GAAAAAGAAAAAGAA	55658
rs531786205	snp	C/T	0.00358779	0.0422022	intron-variant	RNF126	GRCh38.p7	19:652542	ATGTGGGTAGGGCCC[C/T]CGTGGCCCCTTCCCC	55658
rs532018001	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:652156	GAGAGCCGGGGAGGC[A/G]AGGTGGGGACAGGCT	55658
rs532081713	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652485	AAACCACGGGTTTCT[C/G/T]GATAAACCGGTGCAG	55658
rs532144549	snp	A/C	0.00159617	0.0282053	intron-variant	RNF126	GRCh38.p7	19:648650	GGGACCTGGACAGAA[A/C]CCTCTCCTCCCAGCC	55658
rs532348591	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:651983	TGGGAGGGAGACGCA[A/G]ACAGGGAGGCAGGAA	55658
rs532384271	snp	A/G	0.000591774	0.0171912	intron-variant	RNF126	GRCh38.p7	19:648340	GGGAGGGCCGCGGTC[A/G]GGGTGGGGGGGCGGG	55658
rs532481185	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:660030	TCAGCCTCCCAAAGC[A/G]ATGGGACCACAGGCG	55658
rs532526403	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:654116	AGGGCCGACAGCTGG[A/G]CCCCCGCCCACACCA	55658
rs532554658	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF126	GRCh38.p7	19:664168	TCCCGCCTCAGCCTC[C/T]CGAGTAGCTAGGACT	55658
rs532684027	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	RNF126	GRCh38.p7	19:663607	GCTCTCCCGACGCCC[G/T]CGTGGCTTTCTTCCA	55658
rs532710728	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:658973	ACCCCAGCGCCAGCC[A/G]GCCAGAGAGGGCAGC	55658
rs532774949	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:654073	ACTCTGGGGAGAAGC[A/G]GGGGTCTGGCGTGCA	55658
rs532889346	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:654343	CGCCCCACGAATTCT[C/T]GGCACGCTCCGCCAT	55658
rs532897621	snp	G/T	0.00159617	0.0282053	intron-variant	RNF126	GRCh38.p7	19:658314	GGCCCAGGGCCAGGC[G/T]CATGGAGGGGAGTGG	55658
rs532898875	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:662386	AACACCTGGAGGAAG[A/G]GTGGGCTGCGCAGCC	55658
rs532916748	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653313	CCCGTTCCCCTGGCT[C/T]GGGGGAGGCCACGTC	55658
rs532952755	snp	C/T			upstream-variant-2KB	RNF126	GRCh38.p7	19:664799	GGCTGGGCACCACCA[C/T]GCCCGCCTAATTTTT	55658
rs532977089	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:651284	AGGAGTGGGGCCCTG[C/T]GACGGCTCCCCCAGG	55658
rs533158023	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:651507	CTCTCCAGAGAGCCT[A/G]TGGATGATGCCACGT	55658
rs533172800	snp	C/T	0.000569381	0.0168632	intron-variant	RNF126	GRCh38.p7	19:652785	ACAACAGCTGAGGCC[C/T]GGCTGGCTCTTCCAG	55658
rs533179088	snp	A/G	0.00268735	0.0365575	intron-variant	RNF126	GRCh38.p7	19:650311	CCTGGAAAAGAGAGC[A/G]CCAGTCACGGGGTGA	55658
rs533229556	snp	C/T	0.0023933	0.0345097	utr-variant-3-prime	RNF126	GRCh38.p7	19:648055	GCCGGGGCACCCAGT[C/T]TGTGGGTGCCGTGTG	55658
rs533331267	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RNF126	GRCh38.p7	19:647233	GGGGCCAGGAACCCG[C/T]GTGGCTGAGGTGTGA	55658
rs533374400	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653009	GCACACGCAGGCCAG[A/G]GTGGCTCCCAACCCG	55658
rs533435465	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:650566	GGGACCACAGAAGAG[A/G]TCCACCACTCTCGGC	55658
rs533490002	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:662002	TTTGCACGTCAGCCT[A/G]GCGAAGGGCAACACG	55658
rs533525167	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF126	GRCh38.p7	19:665152	CACGCTCCGCAAGTG[C/T]AGGAGGAGCAGCAGG	55658
rs533879015	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:649542	GCTGCCCCCTGTGCC[C/T]GCCAGAGCGTGGAGG	55658
rs533922167	snp	A/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:660606	TCCCTCCCCAGAACA[A/T]ACGCCAGGTGTGCCC	55658
rs533929053	in-del	-/GG/GGG	0.41141	0.19091	intron-variant	RNF126	GRCh38.p7	19:649220	CCCTGACAGCGGAAT[-/GG/GGG]GGGGGGGGGGGCCGC	55658
rs533931610	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:655435	AGCTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC	55658
rs533932392	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:655788	AGCACAGTTCATCAT[C/T]GTCGTCGGCAGATGC	55658
rs533935755	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:651266	CCCAGGCTCCGTTCC[A/G]CCAGGAGTGGGGCCC	55658
rs533981587	snp	C/T			upstream-variant-2KB	RNF126	GRCh38.p7	19:663767	GACACACAGCAGGCA[C/T]TCCCTCAGCGCTGCG	55658
rs534158046	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:654234	GCACATGAACCCACC[A/G]TGAGGGGAGAGTGAA	55658
rs534314034	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF126	GRCh38.p7	19:647804	AAACCATGCATGGCC[A/G]CCACGTGAGCTCAAA	55658
rs534316033	snp	C/T	0.0023933	0.0345097	intron-variant	RNF126	GRCh38.p7	19:651551	GTGCTGGATTCTAAG[C/T]GCCAGAACTTCCGAC	55658
rs534320189	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:656851	CAGTCAAATCTGAAC[C/T]CCTGGTTTCTGCCGG	55658
rs534400445	snp	C/T	0.000285063	0.0119352	intron-variant	RNF126	GRCh38.p7	19:649024	CTCGGGGGCCCGGCC[C/T]GGGGCTCTGAAACGC	55658
rs534482320	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, utr-variant-5-prime	RNF126	GRCh38.p7	19:663265	CGGGGGCGCGGGAGC[A/G]GCGAAAGCTGCGTAC	55658
rs534548997	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:657888	CTGGGGGTCTCCAGC[C/T]GCCCTCCTCCTCCAA	55658
rs534589602	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF126	GRCh38.p7	19:663810	ACCCGGGGCTCAGGG[C/T]GCTGTCTGGGCCTCA	55658
rs534613412	in-del	-/TTTG	0.00287533	0.0378074	upstream-variant-2KB	RNF126	GRCh38.p7	19:664640	CATTTAGATTTTTTG[-/TTTG]TTTGTTTGTTTGTTT	55658
rs534645152	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:659099	CAGCTGTGCAGAGCC[A/G]CTCCAGGGTGCTGGC	55658
rs535041204	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653690	CATGGTGCCTCCCGG[C/G]CTCACCAGGGGCTGG	55658
rs535067179	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:656502	AAAAATACAAAAATT[A/G]GCTGGGCACGGTGGT	55658
rs535127956	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652654	CCGGCCCGGCCATCA[C/G]AGAAGAGAACGGCAC	55658
rs535172859	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:662559	CAGCGAGGCGCCGGC[A/G]CCCCCAACCACGCGC	55658
rs535246208	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653360	CTGCAAGACCCCATC[C/T]CCAGGTCCCCCTAGA	55658
rs535391688	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:657362	CTCAGTCCAGGGCAC[A/G]ACGCATGCTCCCGCC	55658
rs535399688	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:658476	ATGGTGCAGTGCTCG[A/G]CCTCGGTAGGAGCCC	55658
rs535410432	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652444	AGCATTTGGTGCCGT[A/G]ACCCGCTGCTGCTTC	55658
rs535412442	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:649115	GAGCCCGCCCGGGGT[C/T]GGAGATCACTGTGGA	55658
rs535473840	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:649443	TGGGCGAGTCCTCCC[C/T]GCGGTTTTGCTACAA	55658
rs535641949	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:650365	CGCCAGGCCTGCCAG[C/G]TCCGTGGTGAGCACC	55658
rs535655636	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	RNF126	GRCh38.p7	19:647040	TCCTCTCCGTTAGCT[A/G]TCTCCATCGTCTGAT	55658
rs535663641	snp	C/T	0.0023933	0.0345097	intron-variant	RNF126	GRCh38.p7	19:650926	TAGAGATGGGGCCTC[C/T]CTACATTGCTCAGGC	55658
rs535742297	in-del	-/GCCCTGAGCTTAGTGT	0.00398564	0.0444627	intron-variant	RNF126	GRCh38.p7	19:656705	ACGACCACCACTGTG[-/GCCCTGAGCTTAGTGT]GGGAGCAGTGTGGCT	55658
rs536024214	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:660060	GTGAGCCACCGCGCT[C/T]GGCCTCATCACAGCC	55658
rs536327149	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:659066	CAGGGTGCTGCAGGG[A/G]GCCCGTTCCGGAGAA	55658
rs536339932	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	RNF126	GRCh38.p7	19:664377	TTCACTCAACACTCA[C/T]TGAGCAACTACTGCA	55658
rs536448565	in-del	-/GT			intron-variant	RNF126	GRCh38.p7	19:649223	TGACAGCGGAATGGG[-/GT]GGGGGGGGCCGCGCT	55658
rs536604555	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:653324	GGCTCGGGGGAGGCC[A/G]CGTCCACGCTGGCCA	55658
rs536781041	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:654136	CGCCCACACCACGCC[A/G]TGCCTGCCTCACCTG	55658
rs536844251	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:654303	TCCTGGTGAGGCCGG[A/G]AGGCACCACATGCGT	55658
rs536870159	snp	A/C/T	0.000250195	0.0111824	intron-variant	RNF126	GRCh38.p7	19:648516	CAGCTGCGGTCACAG[A/C/T]GGGCGTGGGGGGCCT	55658
rs536935097	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:662680	CTCTGCTCGCCGGGC[C/T]TCAGTTTCTCCGTTT	55658
rs536977067	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:648697	CTCGAGGCCGGGTGC[A/G]GTGGCTCACGCCTGT	55658
rs537211260	snp	C/T	0.00199481	0.0315187	intron-variant	RNF126	GRCh38.p7	19:656923	CCGTCCGCCCGCCAG[C/T]TGACCGGGAGCCCAG	55658
rs537320424	in-del	-/TGCA	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:661989	ACTAAATCACCACTT[-/TGCA]CGTCAGCCTGGCGAA	55658
rs537353156	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	RNF126	GRCh38.p7	19:663174	GCGGCACCCGCCGCC[A/G]GCCGTTTGCTGCTCC	55658
rs537386841	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:653143	ACGGGCGTCACCAGC[A/G]TCATCAGCGCCTTGG	55658
rs537616639	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:662082	CCAGCGTTTTGGGAG[C/G]CTGAGCCAGAAGAAT	55658
rs537658675	snp	C/G	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:650098	CCCTCCTACTCACCA[C/G]GGGCCCAGGCTGGGG	55658
rs537802437	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:655267	TCCAGGAGATCGAGA[C/T]CGCAGTGAGCTGTGG	55658
rs537864812	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652222	GGAAGCACGAGGGGC[A/G]GGCGACTCACCTCCA	55658
rs537919173	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:655825	CTCCAGTGTCCACCC[A/G]CACCTCAGAGCACGA	55658
rs537981971	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:649072	AAAAGCACCGAGGCC[A/G]CGTTTGTCCTGGGCC	55658
rs537982441	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:656454	AGGTTAGGAGTTCGA[A/G]ACCAGCCAACATAGG	55658
rs537982514	snp	C/T	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:652502	ATAAACCGGTGCAGA[C/T]CCCAACAGCCTCCTA	55658
rs537993973	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652640	ACTCCCCTCTGGCCC[C/T]GGCCCGGCCATCACA	55658
rs538194321	snp	G/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652102	CAATCCCTGGCCCGG[G/T]CCCCTGGAGGGAAAA	55658
rs538252211	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:648826	ATACAAGTATGAGCC[A/G]GGCGTGGCGGCGGGT	55658
rs538253769	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:648491	CGAGCCCGGAGCCTG[C/T]GGGAGTGTGCAGCTG	55658
rs538412610	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:659261	ACCAGGAGAAGACAG[C/G]GTGGGCCGGGGGGCA	55658
rs538520476	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF126	GRCh38.p7	19:665208	GAACTGGCTGTGTGT[C/T]CCTAGGCAAGTGGCC	55658
rs538738565	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:663030	CCTGCCGCCCGCCGC[C/T]CCGGCCCGGGCCTCA	55658
rs538991722	snp	G/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:662583	CACGCGCTCGGCGGG[G/T]GTCCCCTGGCGTTAT	55658
rs539002106	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653184	CCGACCTGCCCCACC[A/G]TGACGGGCGTCACCA	55658
rs539005565	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:657421	ACCTGGCCACATACA[C/T]ACTCATCTGCCCCAG	55658
rs539084251	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:650440	TATTTTACTATGAGC[C/T]AGGGTCTCACTCTAA	55658
rs539115692	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:658099	CACCTCTCCGTCAGA[A/G]AACAGATGCAGGAGG	55658
rs539180652	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:658524	TTCCTAAAGGGTGCC[C/T]AAAGCTTCCCGGCTG	55658
rs539194707	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653766	CTGGAAGCTAAATCA[A/G]CTGCTCTCTATGAAC	55658
rs539223087	in-del	-/CCCCAACAG	0.00755907	0.0610114	intron-variant	RNF126	GRCh38.p7	19:652501	ATAAACCGGTGCAGA[-/CCCCAACAG]CCCCAACAGCCTCCT	55658
rs539413382	snp	A/G			upstream-variant-2KB	RNF126	GRCh38.p7	19:664206	CCCGCCACCACACCG[A/G]CTAATTTTTGTATTT	55658
rs539511556	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:657023	GGTGACTCCCCAGGC[C/T]AGCACCACCCAGTGG	55658
rs539556134	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:650955	GCTGGTCTTAAACTC[C/T]TGTCCTCAAGAGATC	55658
rs539655724	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	RNF126	GRCh38.p7	19:647670	CCGGGTCGTGGAGGC[A/G]GCCGAGGGGGAGGCT	55658
rs539726198	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:661635	CAACTCTAGCACTCG[C/T]TCCTCCTCTGTGACC	55658
rs539755530	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:661134	CTCCCCAGGCCCAGT[A/G]ACAGTCGGAGGAGGT	55658
rs539821222	snp	G/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:649960	CCCTCCTACTCACCA[G/T]GGACCCTGGCTGGGG	55658
rs539922156	snp	C/G			utr-variant-3-prime	RNF126	GRCh38.p7	19:647656	CGAGCCCCCCTACTC[C/G]GGGTCGTGGAGGCGG	55658
rs539998380	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:652134	TTTCCTCCGCCGTGC[A/G]GGCAGGGAGAGCCGG	55658
rs540204556	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:659763	AGACACCCTCGTCAT[C/T]GCCTTTTTTTTTTTT	55658
rs540219467	snp	C/T	0.0107869	0.0726437	synonymous-codon, intron-variant	RNF126	GRCh38.p7	19:651655	GCCGGTGGCCCGCCG[C/T]GTGGTGAGGCGGGCG	55658
rs540526183	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:654944	TGTAACTCCAGCCTG[A/G]GCGACAGAGTGAGAC	55658
rs540735942	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:662755	CGCGGCCTCTCGGGT[A/C]GGGAACGCCGCGGAT	55658
rs540859346	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF126	GRCh38.p7	19:663555	CGTTCCTGGGGCTCG[C/T]CAGGCGCCCTCTCCC	55658
rs540907839	snp	G/T			intron-variant	RNF126	GRCh38.p7	19:649168	TGGGTCCCCTGACGG[G/T]GGAATGGGGGAATGG	55658
rs540909995	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:658609	CACCCCTTTCTTCCC[A/G]CCCTCAGCAGCTGCC	55658
rs540934945	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:659484	CAGAGCTGGAACCAC[C/T]CTAGGAACCACCCAG	55658
rs540956786	snp	A/G	0.00159617	0.0282053	intron-variant	RNF126	GRCh38.p7	19:653635	GCCCCTGGTGATGGC[A/G]GAGCGTGCCGAGCAT	55658
rs541011725	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653880	GTCCCAAGACCACCC[C/T]CAGGTAACACAGACA	55658
rs541036203	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:656718	TGGCCCTGAGCTTAG[C/T]GTGGGAGCAGTGTGG	55658
rs541148370	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652766	CAGCACAGCCCACAC[C/T]CCTACAACAGCTGAG	55658
rs541183839	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:650529	CTTAAGCGATCCTCC[C/T]GCCTCAGCCTCCCAA	55658
rs541246072	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RNF126	GRCh38.p7	19:647169	GAGCTGGCTGCACCC[C/T]GGGCCAGGCATCCAG	55658
rs541333132	in-del	-/AG	0.00438332	0.0466095	intron-variant	RNF126	GRCh38.p7	19:656005	CCGAGCCACAGAGAC[-/AG]AGAGGGGATGTGTGA	55658
rs541357308	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	RNF126	GRCh38.p7	19:647509	CACGGGCGCAGAAGG[A/C]AAGCCACAGCACCGG	55658
rs541410005	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:661749	TGGACTTCTCTTACG[A/G]GTCAAAGCGTAGCAA	55658
rs541563733	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652988	CAGCGGTCTCTGGCT[A/G]GCCAGGCACACGCAG	55658
rs541584110	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:653687	GTGCATGGTGCCTCC[C/T]GGCCTCACCAGGGGC	55658
rs541803198	snp	C/T	0.0023933	0.0345097	intron-variant	RNF126	GRCh38.p7	19:649235	TGGGGGGGGGGGCCG[C/T]GCTCCTGAGTGCCCT	55658
rs541807137	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652523	CAGCCTCCTAAGCGT[C/G]AGAATGTGGGTAGGG	55658
rs541866598	snp	C/T	0.000798403	0.0199641	missense	RNF126	GRCh38.p7	19:649690	GTACCTGTGTGATGA[C/T]GGCATCCAGGCCGTT	55658
rs542030351	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:660391	AAGCCCTCGTGGGCA[A/G]GCACACAGCCCATGG	55658
rs542048819	in-del	-/GAGGCCC	0.0011981	0.0244461	intron-variant	RNF126	GRCh38.p7	19:652778	ACCCCTACAACAGCT[-/GAGGCCC]GAGGCCCGGCTGGCT	55658
rs542145462	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:655560	CTGGGTAAACGCAGC[C/T]GGCCAGCCCCAGCGA	55658
rs542152790	snp	A/C	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:661222	CCAGTCCTGTGCGGG[A/C]TCTAGGAGCAGCTAA	55658
rs542164498	snp	G/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:659689	TCCAGCTGGCCTGTC[G/T]GGTTCCTGCCGCCAC	55658
rs542373421	snp	A/G	0.000118543	0.00769789	intron-variant	RNF126	GRCh38.p7	19:651965	GCCCTGCTGGGTGCC[A/G]GGTGGGAGGGAGACG	55658
rs542406856	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:654280	ATATAGAAAAAGTGC[A/G]GCCCGGCTCCTGGTG	55658
rs542434877	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:648573	CACAGCCTCAGCCGG[A/C]GGCCGCCCCTGAGCC	55658
rs542557624	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:655883	GACCAGGCCACGGCG[A/G]GGGGGAGGGGGGATT	55658
rs542582761	snp	C/G	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:658780	GGCCCAGGCCCCGAA[C/G]TCTGCCTTCTTCTTC	55658
rs542593894	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652354	CCCCATGCGCCAGGC[A/G]CTCCCTCCCCTCAAA	55658
rs542693013	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653985	GGATGCAGGTTGCAC[C/T]GGGGCTGTTCAGTCT	55658
rs543007150	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653464	GGTGAGTCCCAAAAC[A/C]ACGTTCACAGTTCCC	55658
rs543009019	snp	C/T	0.00159617	0.0282053	intron-variant	RNF126	GRCh38.p7	19:651158	AGCAGGGCCCAGCGA[C/T]GGCTCCCCCAGGCTC	55658
rs543012363	snp	C/T	0.00438332	0.0466095	intron-variant	RNF126	GRCh38.p7	19:652016	GGGCAGAGCCTGCCC[C/T]GCTGGTGTGAGATGC	55658
rs543012704	in-del	-/G			intron-variant	RNF126	GRCh38.p7	19:652812	CCAGCCTCTTCAACA[-/G]GGGGCTGCATTACCT	55658
rs543120954	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:651407	CCCACTCTGTGGTCA[A/C]CCCACACACCCTGAA	55658
rs543149161	snp	A/G	0.0142173	0.0831054	utr-variant-3-prime	RNF126	GRCh38.p7	19:647978	GGGGGCCGGTGGGCC[A/G]GGCCCGGGTCCTGCC	55658
rs543163874	snp	C/T	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:661944	CACCACGCGCCTCAG[C/T]TTCCCCATCTATAAA	55658
rs543353686	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:658259	CAGGGCAGCAGAGGC[C/T]CCTTCATCCACGGGG	55658
rs543354822	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB	RNF126	GRCh38.p7	19:663432	GCGTGCGCGGGGCGG[A/G]GCCGAGGCCCTCCTC	55658
rs543361784	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RNF126	GRCh38.p7	19:647135	GCCCGCAGGTCCCCA[C/T]GCCTTGCCAGCTGTG	55658
rs543477923	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:660876	ATGCTGTCTACGGGC[A/G]CCTTGTTGCGTCCTG	55658
rs543501560	snp	C/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:656071	GGCTGGCAGGGCTGA[C/G]GTGGGTTCTTTTTGC	55658
rs543577761	snp	A/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:662280	CCCCAAGGTGACATC[A/T]GGTCCGCGTGGGAAA	55658
rs543721976	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:660160	CTCAGGACACCCTCA[C/T]GAGTCACCAGGAGAG	55658
rs543738212	snp	C/T	0.000399281	0.0141238	missense	RNF126	GRCh38.p7	19:650276	GGCGTGATGATGCCG[C/T]TGACGAGCTGCTGGA	55658
rs543742781	snp	A/G	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:653276	TGGCATTTCCAGGAC[A/G]CTCTGGCAGCCCCGC	55658
rs543830843	in-del	-/G	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:662732	TTAGGGATCCCACCT[-/G]GGATCCTCGCGGCCT	55658
rs543887377	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:661123	ACAGGAAGGCCCTCC[C/T]CAGGCCCAGTGACAG	55658
rs544019234	snp	C/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:649169	GGGTCCCCTGACGGT[C/G]GAATGGGGGAATGGG	55658
rs544190496	snp	A/G	0.0111196	0.0737302	intron-variant	RNF126	GRCh38.p7	19:652165	GGAGGCGAGGTGGGG[A/G]CAGGCTGGCGCTCGG	55658
rs544230009	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:648547	GCCGAGCCTTCAAGG[A/G]CAGGCTACTCCACAG	55658
rs544300626	snp	C/T	0.000288996	0.0120173	intron-variant	RNF126	GRCh38.p7	19:652340	CGGCTACCCTGTGCC[C/T]CCATGCGCCAGGCGC	55658
rs544320027	snp	C/T			upstream-variant-2KB	RNF126	GRCh38.p7	19:664573	GAGTTGGACTTCCTG[C/T]AAAATGAGGCATTGG	55658
rs544344734	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:649622	GTGGGGCAGCTCCCA[A/G]GGGTGGGCAGCCCAG	55658
rs544432443	snp	G/T	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:655502	AAAAAAAAGAAAAGT[G/T]GGGGGGGAAAGGACG	55658
rs544568208	snp	C/T	0.00199481	0.0315187	intron-variant	RNF126	GRCh38.p7	19:659849	GCTCACTGCAACCTC[C/T]GCCTTCCAGGTTCAA	55658
rs544707456	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	RNF126	GRCh38.p7	19:664173	CCTCAGCCTCTCGAG[A/T]AGCTAGGACTAGAGG	55658
rs544891128	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:660235	CACGGGGAGCGAATC[A/G]CATCACTAAACCCAC	55658
rs544921282	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:654959	GGCGACAGAGTGAGA[C/T]TCCGTATCGGGAAAA	55658
rs545016269	snp	G/T	0.00318978	0.0398085	intron-variant	RNF126	GRCh38.p7	19:662845	GGGCCTCAGTCTCCC[G/T]CATGTACAGGACGGG	55658
rs545041430	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653012	CACGCAGGCCAGGGT[A/G]GCTCCCAACCCGTGG	55658
rs545115320	snp	C/T	0.00478085	0.0486577	intron-variant	RNF126	GRCh38.p7	19:649951	ACAGGCACCCCCTCC[C/T]ACTCACCAGGGACCC	55658
rs545524116	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:651116	GTAGGGCCCTGCGAC[A/G]GCTCCCCCAGGCTCT	55658
rs545536516	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF126	GRCh38.p7	19:647635	TGCTGGTCATCCTCA[C/T]GGTCCCGAGCCCCCC	55658
rs545579915	snp	C/G/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:655884	ACCAGGCCACGGCGG[C/G/T]GGGGAGGGGGGATTG	55658
rs545744650	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:650167	GGCTGGGGATGGGGA[C/T]AGGCACCCCCACCCA	55658
rs545887235	snp	A/G	0.00597247	0.0543191	intron-variant	RNF126	GRCh38.p7	19:660455	AGCTTCCCGACAGCC[A/G]GCCCAGGTGTCTCAG	55658
rs545891170	snp	A/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:661987	CGACTAAATCACCAC[A/T]TTGCACGTCAGCCTG	55658
rs545930060	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652641	CTCCCCTCTGGCCCC[A/G]GCCCGGCCATCACAG	55658
rs545956206	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	RNF126	GRCh38.p7	19:647110	TGAACCCACTGCCCC[A/G]GCCCCCTGAGCCCGC	55658
rs546069521	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:661822	CTGCAGCCTCTTCCC[C/G]TGGGCACAGGGTGGG	55658
rs546071839	snp	C/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:656625	TGCACTCCAGCCTGG[C/G]CCACAGAGTGAGACC	55658
rs546125624	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:657292	CTGGTCCCCATGTGC[C/T]GAGCTCAGCCCCTCT	55658
rs546169744	in-del	-/A	0.00279162	0.0372561	intron-variant	RNF126	GRCh38.p7	19:658615	TTTCTTCCCGCCCTC[-/A]GCAGCTGCCACCACA	55658
rs546170889	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:659984	TAGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA	55658
rs546219535	snp	A/G	0.000234348	0.0108221	synonymous-codon	RNF126	GRCh38.p7	19:649741	TAGGGTTTGAGTGCA[A/G]GACTCCCCTGGAGGT	55658
rs546244262	snp	C/G	5.10782e-05	0.00505336	missense	RNF126	GRCh38.p7	19:651785	GTGGGGATCTCGAAG[C/G]TGTCATCGAAGATGC	55658
rs546336950	snp	A/C	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:648621	CCGTGTGTGTGTCCC[A/C]CGGGCTGCCAGAGGG	55658
rs546506578	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:659652	TCGAGTCTGGGTCTG[C/T]GCAGCCGCCTGTGGC	55658
rs546522526	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652716	GAGCCACAGACACCA[C/G]GGCCTGACGGCCCCA	55658
rs546532370	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RNF126	GRCh38.p7	19:664332	ACAGGCATGAGCCAC[C/T]GCGCCCGGCCTCATG	55658
rs546659402	snp	C/T	0	0	intron-variant	RNF126	GRCh38.p7	19:652015	TGGGCAGAGCCTGCC[C/T]CGCTGGTGTGAGATG	55658
rs547021510	snp	C/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:661965	CATCTATAAAGCACG[C/G]GTGGCTCGACTAAAT	55658
rs547070999	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:662574	GCCCCCAACCACGCG[C/T]TCGGCGGGGGTCCCC	55658
rs547110718	snp	C/T	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:656836	CACGCTGAGACTTCA[C/T]AGTCAAATCTGAACC	55658
rs547134074	snp	A/G	0.00358779	0.0422022	intron-variant	RNF126	GRCh38.p7	19:662963	GCGCAAGAGGCGGGC[A/G]CAAGCGACCCCCACC	55658
rs547231769	snp	C/T	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:652034	TGGTGTGAGATGCCT[C/T]GGTGGAAGTTTCGCT	55658
rs547246505	snp	C/T	0.00398564	0.0444627	intron-variant	RNF126	GRCh38.p7	19:658437	TCGGGAAGCTGTGCA[C/T]ATCAGGAGACCCCAG	55658
rs547472539	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:649946	TGGGAACAGGCACCC[C/T]CTCCTACTCACCAGG	55658
rs547479140	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653116	GAGCCCCTCCGACCT[A/G]GCCCCACCGTGACGG	55658
rs547535358	snp	A/C/G/T	0.0001162	0.00762161	intron-variant	RNF126	GRCh38.p7	19:650305	GATGATCCTGGAAAA[A/C/G/T]AGAGCGCCAGTCACG	55658
rs547697470	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:651241	AGGAGTGGGGCCCTG[C/T]GACGGCTCCCCCAGG	55658
rs547702165	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:661525	CTTTATTTGTTCCTC[C/T]TGCTGGGGAGGGGAA	55658
rs548127232	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:654123	ACAGCTGGGCCCCCG[C/T]CCACACCACGCCGTG	55658
rs548195585	snp	C/T	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:652448	TTTGGTGCCGTAACC[C/T]GCTGCTGCTTCCCTC	55658
rs548264150	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF126	GRCh38.p7	19:665056	CACCAGAGAGCGCAC[A/G]GGCCCCGTCCCTGGG	55658
rs548388385	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:659602	CTCGCCCACACCCTA[C/T]AGTCACAGCTCCAGT	55658
rs548400532	snp	C/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:654385	CGGTGGCTCAGGCCT[C/G]TAATCCTGGCACTTC	55658
rs548436367	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:660590	AGATACGGAGCAGCC[A/G]TCCCTCCCCAGAACA	55658
rs548596981	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:659070	GTGCTGCAGGGAGCC[C/T]GTTCCGGAGAACCCA	55658
rs548726473	snp	C/T	0.000655762	0.0180956	synonymous-codon	RNF126	GRCh38.p7	19:648408	GCAGCCGTCGTGGAA[C/T]AGGTGGTTGCAGGGC	55658
rs548737607	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:655018	AAAGAAAGAAAGAAA[A/G]AAAAGCCCAGGCCAG	55658
rs548848660	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:655967	AGCGTGTGATCCCAC[A/G]TCTATGAAATGTCCA	55658
rs548886361	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RNF126	GRCh38.p7	19:663765	CTGACACACAGCAGG[C/T]ATTCCCTCAGCGCTG	55658
rs548886956	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652178	GGACAGGCTGGCGCT[C/T]GGGGCCCCGAGCAAG	55658
rs548886992	snp	G/T	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:648711	CGGTGGCTCACGCCT[G/T]TCATCCCAGCACTTT	55658
rs548894790	snp	G/T			intron-variant	RNF126	GRCh38.p7	19:653546	TGTGGATCTCACACT[G/T]CAACGGGATCCCCAG	55658
rs549085480	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:653034	AACCCGTGGGTCCTG[C/G]AGGGCGGCCGAGGGG	55658
rs549188111	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF126	GRCh38.p7	19:647642	CATCCTCATGGTCCC[A/G]AGCCCCCCTACTCCG	55658
rs549277353	snp	A/G	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:653326	CTCGGGGGAGGCCAC[A/G]TCCACGCTGGCCACA	55658
rs549280919	snp	C/G			upstream-variant-2KB	RNF126	GRCh38.p7	19:665133	CAGCCCCTGCACCAG[C/G]CTTCACGCTCCGCAA	55658
rs549317321	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	RNF126	GRCh38.p7	19:647273	GGGGCAGAGGCGCTG[C/G]GCCCTGGCGCTTTAA	55658
rs549547071	snp	A/G	0.00199481	0.0315187	intron-variant	RNF126	GRCh38.p7	19:661014	CATGATTAAATATTT[A/G]TCAATCACTGTTCCA	55658
rs549588981	snp	A/G	0.0193772	0.0965046	intron-variant	RNF126	GRCh38.p7	19:662523	CCAAGGCGGCGGCCA[A/G]GGCTCCACGAGGCGA	55658
rs549650260	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:658006	CTGCCCCACCTTCTC[C/T]GGGGGCAGCACGCAC	55658
rs549696972	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:662864	GTACAGGACGGGGTT[A/C]GCGCGCGCACCGCCC	55658
rs549795266	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:650737	AGCTGGGATTACAGG[C/T]GCCCACCGCCATGCC	55658
rs549846901	snp	G/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:661372	CAGGCTGGCGGGCTG[G/T]CAGGCAACCAGCCTC	55658
rs549853640	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652423	CTTCCCACCCGCCAC[C/T]GCCCCAGCATTTGGT	55658
rs549858696	snp	G/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:656791	CTTGGGGTGTGTTTG[G/T]GGTGTCGGGATTGGG	55658
rs550011507	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:649382	AGCAGGTCAGGGCGC[A/G]ACCTCTCGGGAAGAG	55658
rs550084017	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653049	GAGGGCGGCCGAGGG[A/G]ACCTGGCCTCTGCCA	55658
rs550146389	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:650896	CTCACCCAGCCTCAG[C/T]TACTTTTTAAAAATT	55658
rs550314974	snp	A/G	9.43708e-05	0.00686851	intron-variant	RNF126	GRCh38.p7	19:649795	ACGGGCAGCTGGGGC[A/G]GGTGCGTCTATCCAC	55658
rs550539053	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RNF126	GRCh38.p7	19:664985	TGGGGACAGGGGCTT[A/C]AGCCTCCTTCCAGTC	55658
rs550599240	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:660951	GACACGGGCAGGCCC[C/T]CGCAGCCCTCTCTGC	55658
rs550600338	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:660044	CGATGGGACCACAGG[A/C]GTGAGCCACCGCGCT	55658
rs550631648	snp	A/G	2.58008e-05	0.00359162	synonymous-codon	RNF126	GRCh38.p7	19:648922	GGTGGGGAGGGCCTG[A/G]ATTTTCTCTTTATCT	55658
rs550651721	snp	C/G	0.00159617	0.0282053	intron-variant	RNF126	GRCh38.p7	19:655621	GATGCAAGACCCCGT[C/G]AGGCCTGCTGGGAGC	55658
rs550748775	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RNF126	GRCh38.p7	19:663608	CTCTCCCGACGCCCG[C/T]GTGGCTTTCTTCCAG	55658
rs551180295	snp	C/T			downstream-variant-500B	RNF126	GRCh38.p7	19:647500	TTCCTGACGCACGGG[C/T]GCAGAAGGAAAGCCA	55658
rs551182154	snp	G/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:659572	GTTCCTGGGGGCTCA[G/T]TGCCCTCAGCAGCTC	55658
rs551224314	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:654121	CGACAGCTGGGCCCC[C/T]GCCCACACCACGCCG	55658
rs551255571	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:651510	TCCAGAGAGCCTATG[A/G]ATGATGCCACGTTTC	55658
rs551351113	snp	A/C			upstream-variant-2KB	RNF126	GRCh38.p7	19:664924	GGGATTACAGGCGTA[A/C]GCCACCGCGCCCGGC	55658
rs551361902	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RNF126	GRCh38.p7	19:648064	CCCAGTCTGTGGGTG[C/T]CGTGTGGCGCTGGCT	55658
rs551456478	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:651288	GTGGGGCCCTGCGAC[A/G]GCTCCCCCAGGCTCT	55658
rs551500202	snp	A/G	0.00159617	0.0282053	downstream-variant-500B	RNF126	GRCh38.p7	19:647234	GGGCCAGGAACCCGC[A/G]TGGCTGAGGTGTGAC	55658
rs551521887	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	RNF126	GRCh38.p7	19:647676	CGTGGAGGCGGCCGA[A/G]GGGGAGGCTGGGGGC	55658
rs551669645	snp	A/G	0.00199481	0.0315187	intron-variant	RNF126	GRCh38.p7	19:657459	CTCCTCTTGGCCCCC[A/G]CTGTCCTGCCCGCAG	55658
rs551803607	snp	A/C	0.00279162	0.0372561	intron-variant	RNF126	GRCh38.p7	19:662401	GGTGGGCTGCGCAGC[A/C]AAGCCCCGGGAGGGG	55658
rs552004000	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:662042	TGCAGACCACCGCCG[A/G]GCACGGTGGCTCACA	55658
rs552181402	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652622	GCTGCACAGGTTGCC[A/G]GCACTCCCCTCTGGC	55658
rs552184077	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:654500	ATACAAAAATTAGCC[A/G]GGTGTGGTGGCGGGC	55658
rs552317475	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:660931	TTGGGATCACCCGCG[A/G]GGTGGACACGGGCAG	55658
rs552430468	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:661325	CTGTCCCAGGGCTCA[A/C]GGGGCTGCAAGGGGC	55658
rs552432161	snp	A/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:656307	GTGAGCCAAGATTGC[A/T]GCAACAGAGTGAGGC	55658
rs552459963	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:649040	GGGGCTCTGAAACGC[A/G]AGGCTGCAGGACCTG	55658
rs552492327	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:656765	GTGACAACTCTCCCC[A/C]GGCGTCGGTTCTTGG	55658
rs552705646	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652396	GGAGAGCAGGAATTG[C/T]CCTTGGCACTGCTTC	55658
rs552726868	snp	C/T	0.00478085	0.0486577	upstream-variant-2KB, utr-variant-5-prime	RNF126	GRCh38.p7	19:663296	TCGGCGGGCAGCGGC[C/T]CGGGCGACGGTGGCC	55658
rs552787681	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:658622	CCGCCCTCAGCAGCT[C/G]CCACCACATCCCACA	55658
rs552789627	in-del	-/C	0.00358779	0.0422022	intron-variant	RNF126	GRCh38.p7	19:662623	CCGAGCCCCGCCAGG[-/C]CCAGCCCCTGCCCCG	55658
rs552789708	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF126	GRCh38.p7	19:663811	CCCGGGGCTCAGGGC[A/G]CTGTCTGGGCCTCAC	55658
rs552856967	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:655369	AACGCAACTAAAAAC[A/G]GGCAAAGTCGGGAGG	55658
rs553009425	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:654240	GAACCCACCGTGAGG[A/G]GAGAGTGAAGAGGCA	55658
rs553082150	snp	C/T	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:657381	CATGCTCCCGCCACC[C/T]GCACTGCCGGCTCAC	55658
rs553183866	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653881	TCCCAAGACCACCCC[A/C]AGGTAACACAGACAA	55658
rs553319883	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653383	CCCCTAGAGCCAAGG[A/C]CAACACAAGGCCAAC	55658
rs553383142	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:661773	GTAGCAACAGCCGGG[A/C]GGCTACGTACACAGC	55658
rs553444882	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:662167	CTAAAAATAATATTA[A/G]AAATGCAGACTGCTG	55658
rs553449839	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:653171	TGGCTGAGCCCCTCC[A/G]ACCTGCCCCACCGTG	55658
rs553457031	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:657604	TTCAAAGGTCACCTC[C/T]CTGCTCCAAGCCTCT	55658
rs553477176	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:659465	GGGGTGGGGGGTCGG[C/T]AGGCAGAGCTGGAAC	55658
rs553522324	snp	A/G	0.00159617	0.0282053	intron-variant	RNF126	GRCh38.p7	19:658044	CCCCACAGAGGCCCC[A/G]TTGGAGCCTCTGGCC	55658
rs553724542	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:649465	TTGCTACAACGTTCC[A/G]CGTGAACACAGGAGA	55658
rs553894926	snp	A/G	0.0532157	0.154195	intron-variant	RNF126	GRCh38.p7	19:650147	TCCTACTCACCAGGG[A/G]CCCTGGCTGGGGATG	55658
rs553988337	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:660806	ACCCCACTAATTGTT[C/T]TAGTCTTCTGTAGAG	55658
rs554326412	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:659749	CTGCTCAGACACCCA[A/G]ACACCCTCGTCATCG	55658
rs554388155	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:654837	CCAGGCGTGGTGGCA[C/T]GTACCTGTAATCCCA	55658
rs554487683	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:653189	CTGCCCCACCGTGAC[A/G]GGCGTCACCAGTGCC	55658
rs554492470	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:651115	AGTAGGGCCCTGCGA[C/T]GGCTCCCCCAGGCTC	55658
rs554649574	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	RNF126	GRCh38.p7	19:664378	TCACTCAACACTCAT[G/T]GAGCAACTACTGCAC	55658
rs554698028	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653828	GTGAAAATGGCCTCA[A/C]ACGGCACGTGTCATC	55658
rs554759049	snp	A/G	0.00159617	0.0282053	intron-variant	RNF126	GRCh38.p7	19:658456	AGGAGACCCCAGGGA[A/G]AGTCATGGTGCAGTG	55658
rs555095692	snp	C/T	0.00101958	0.0225555	intron-variant	RNF126	GRCh38.p7	19:651597	CCTCGCGGCCACCCC[C/T]GGGGCCCCCTCACCC	55658
rs555151701	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime	RNF126	GRCh38.p7	19:647762	GCTTCAGCGCTGGGG[G/T]AGCCGCTGGGCCCCG	55658
rs555171258	in-del	-/T			upstream-variant-2KB	RNF126	GRCh38.p7	19:664049	TGCATTTCTTTTTTC[-/T]TTTTTTTTTTTGAGA	55658
rs555188019	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:662689	CCGGGCCTCAGTTTC[C/G/T]CCGTTTGCAAAACCA	55658
rs555200565	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime	RNF126	GRCh38.p7	19:663181	CCGCCGCCGGCCGTT[C/T]GCTGCTCCCTCGCCG	55658
rs555312064	snp	A/G	0.000798403	0.0199641	downstream-variant-500B	RNF126	GRCh38.p7	19:647493	TGGCCTTTTCCTGAC[A/G]CACGGGCGCAGAAGG	55658
rs555388994	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:651275	CGTTCCACCAGGAGT[A/G]GGGCCCTGCGACGGC	55658
rs555396566	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:658582	CAGAGGCACGGGCAC[A/G]TGCGGCGCCTGCACC	55658
rs555639476	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653151	CACCAGCGTCATCAG[C/T]GCCTTGGCTGAGCCC	55658
rs555647403	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:651052	CACTTTTAAAGATGA[C/G]ATTTCCAGCAGGTGA	55658
rs555716838	snp	A/G	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:657583	TGGAACGCCCACCCT[A/G]GGGGTTTCAAAGGTC	55658
rs555789879	snp	G/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:661731	CACTGCTTCTGGGGG[G/T]CTTGGACTTCTCTTA	55658
rs555849873	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:656968	CTGGGTGGGTCTCTG[A/G]GAATGGAGGGGTAGC	55658
rs555986130	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:656474	GCCAACATAGGGAAA[C/T]ACCGTCTCTACTAAA	55658
rs555992603	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:649663	GCAGGCACTCTGGGC[C/T]GTGGCCACGCTGTAC	55658
rs556231556	snp	A/G	0.00119737	0.0244387	downstream-variant-500B	RNF126	GRCh38.p7	19:647033	TGGAGGCTCCTCTCC[A/G]TTAGCTGTCTCCATC	55658
rs556256084	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:648829	CAAGTATGAGCCAGG[C/T]GTGGCGGCGGGTGCC	55658
rs556303661	in-del	-/A	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:651464	CGTGTGGGGAGTCAC[-/A]GGGGGCTGGAGGGCC	55658
rs556365269	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:650111	CAGGGGCCCAGGCTG[C/G]GGATGGGGACAGGCA	55658
rs556527037	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF126	GRCh38.p7	19:665210	ACTGGCTGTGTGTCC[C/T]TAGGCAAGTGGCCTA	55658
rs556539474	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:660239	GGGAGCGAATCGCAT[C/G]ACTAAACCCACTTGG	55658
rs556605026	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:649074	AAGCACCGAGGCCGC[A/G]TTTGTCCTGGGCCCT	55658
rs556649313	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:660357	AAAGGAGGCCCGGAA[C/T]GGCCCAGCTGCCTGG	55658
rs556772386	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:654266	AGGCACCATCTACAA[C/T]ATAGAAAAAGTGCGG	55658
rs556831883	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:652417	GCACTGCTTCCCACC[C/T]GCCACCGCCCCAGCA	55658
rs556988608	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:658559	ACAGTGTGTGGGCCC[C/T]GCAGCCCCAGAGGCA	55658
rs557043110	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RNF126	GRCh38.p7	19:664348	GCGCCCGGCCTCATG[C/T]GTGTATTTCTTTCTT	55658
rs557156275	snp	G/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:659714	CGCCACACGCCCCAC[G/T]CTGGCTGACGCTCCC	55658
rs557196978	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:657389	CGCCACCCGCACTGC[C/T]GGCTCACGACAGCCC	55658
rs557298780	snp	C/T	0.000902171	0.0212196	intron-variant	RNF126	GRCh38.p7	19:651585	AAGGCGTGGGGCCCT[C/T]GCGGCCACCCCCGGG	55658
rs557357057	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:653130	TGGCCCCACCGTGAC[A/G]GGCGTCACCAGCGTC	55658
rs557362239	snp	C/G	3.12397e-05	0.00395208	missense	RNF126	GRCh38.p7	19:648216	ACCCCAGTGAGGCCA[C/G]GGGGGTTCGTGGCCG	55658
rs557363889	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:661894	CTGGCCAAGCGGCTC[C/T]CGACTGAGCCGGCTC	55658
rs557426584	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:658114	GAACAGATGCAGGAG[A/G]TACGATCACCCGGCA	55658
rs557487881	snp	A/G	0.00358779	0.0422022	intron-variant	RNF126	GRCh38.p7	19:653446	TGCCCAGGGACAGCC[A/G]TGGGTGAGTCCCAAA	55658
rs557505826	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653781	ACTGCTCTCTATGAA[C/T]GACCCAGTCTCAAGT	55658
rs557573997	snp	C/T	0.00159617	0.0282053	downstream-variant-500B	RNF126	GRCh38.p7	19:647465	TCTGCAGAGCCCGAC[C/T]AGCCTCCCAGCTTGG	55658
rs557637985	snp	C/G	7.75044e-05	0.00622464	intron-variant	RNF126	GRCh38.p7	19:648493	AGCCCGGAGCCTGCG[C/G]GAGTGTGCAGCTGCG	55658
rs557764247	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:650474	CGAGGCAGGAGAGAA[A/G]CAGCTTGATCTTGGT	55658
rs557791342	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:662643	CCCCTGCCCCGCGCC[A/G]CGCCACCGGGCAATA	55658
rs557968744	snp	G/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:656631	CCAGCCTGGGCCACA[G/T]AGTGAGACCGTGTCA	55658
rs557982828	snp	A/G	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:652737	GACGGCCCCACACTC[A/G]GCGGGGCGGACGCCA	55658
rs558027323	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:659168	GGTATCTGGCACAAC[C/T]GCAGACACACAGAGC	55658
rs558065919	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:661154	TCGGAGGAGGTCAAG[A/G]TCCTCCGTGTCCAAG	55658
rs558299711	snp	A/G			utr-variant-3-prime	RNF126	GRCh38.p7	19:647904	GTGAGGTTAGACAGA[A/G]GACGGGGAGGCTGGG	55658
rs558310191	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653599	ACTGGCTCACAGGGC[A/G]GACTCCTCATGGATG	55658
rs558383349	snp	C/G	5.23054e-05	0.0051137	intron-variant	RNF126	GRCh38.p7	19:652308	GCTCCTGGGGAGAGA[C/G]TGCAGGTCAGCAGTG	55658
rs558501810	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:649158	CCCCCGCTCCTGGGT[A/C]CCCTGACGGTGGAAT	55658
rs558626272	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:660162	CAGGACACCCTCACG[A/G]GTCACCAGGAGAGCG	55658
rs558636624	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:660642	CCAGCATAAAAAATT[C/T]GTTTTTGAGACAGCG	55658
rs558807713	snp	C/T	0.00159617	0.0282053	intron-variant	RNF126	GRCh38.p7	19:649550	CTGTGCCCGCCAGAG[C/T]GTGGAGGCTGTGCCC	55658
rs558926030	snp	G/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:662362	CCTCTTCGGTGAGGG[G/T]CGGCTGTAAACACCT	55658
rs558988032	snp	G/T	0.00199481	0.0315187	intron-variant	RNF126	GRCh38.p7	19:662797	CGGCCGCGATCCCGC[G/T]GCGCCGCTCCGGCCA	55658
rs558989904	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:657818	TGACAGGTGGATCCC[A/G]GATATCCAGGGTGGA	55658
rs559095305	snp	G/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:648821	TGAAAATACAAGTAT[G/T]AGCCAGGCGTGGCGG	55658
rs559193183	snp	A/C			intron-variant	RNF126	GRCh38.p7	19:653665	TTCGTGGGGCCTGGG[A/C]TGAAACGTGCATGGT	55658
rs559321824	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653551	ATCTCACACTGCAAC[A/G]GGATCCCCAGGGCTG	55658
rs559335765	snp	C/T	0.00159617	0.0282053	intron-variant	RNF126	GRCh38.p7	19:651488	GAGGGCCTGGCCGGG[C/T]GGCCTCTCCAGAGAG	55658
rs559433284	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:650546	CCTCAGCCTCCCAAG[C/T]AGCTGGGACCACAGA	55658
rs559475370	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653306	CACACAGCCCGTTCC[C/G]CTGGCTCGGGGGAGG	55658
rs559536458	snp	C/T	0.00318978	0.0398085	upstream-variant-2KB	RNF126	GRCh38.p7	19:663449	CCGAGGCCCTCCTCC[C/T]CTCCCGAAGCTGCCC	55658
rs559544487	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652990	GCGGTCTCTGGCTGG[C/T]CAGGCACACGCAGGC	55658
rs559545680	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	RNF126	GRCh38.p7	19:647206	TGAGCAGTGGGGTCC[A/G]GCTTTTCAGAAGGGG	55658
rs559561153	snp	C/T	0.000341239	0.0130577	missense, intron-variant	RNF126	GRCh38.p7	19:651650	TGCCGGCCGGTGGCC[C/T]GCCGCGTGGTGAGGC	55658
rs559606833	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	RNF126	GRCh38.p7	19:647534	CACCGGCTTCTCTTT[G/T]TAAGTAGTGTATTTT	55658
rs559611289	snp	C/T	0.000565073	0.0167993	missense, intron-variant	RNF126	GRCh38.p7	19:651665	CGCCGCGTGGTGAGG[C/T]GGGCGCGGGGCTGTC	55658
rs559702759	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF126	GRCh38.p7	19:648036	ACCAGCCAAGCGTGG[C/T]GCCGCCGGGGCACCC	55658
rs559742002	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652769	CACAGCCCACACCCC[C/T]ACAACAGCTGAGGCC	55658
rs559818934	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:657941	GGTCTCGTATTAAAT[C/T]GGGGCAGCTGCAGGT	55658
rs559828253	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:657209	TGCCAGCCCCAGCCC[C/T]GAATCTCTCCTGGAC	55658
rs559970943	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:652752	GGCGGGGCGGACGCC[A/G]GCACAGCCCACACCC	55658
rs560180647	snp	A/G	0.00438332	0.0466095	intron-variant	RNF126	GRCh38.p7	19:659957	TTTAGTAGGGATGGG[A/G]TTTTACCATGTTAGC	55658
rs560180705	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF126	GRCh38.p7	19:665261	ACCTGACGGTTTTCC[A/G]TTGGCTCGGAGCAGA	55658
rs560291772	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:660419	TGGCAGCCAGTCCCC[C/G]CTGCGTCAGAGGCAG	55658
rs560298622	snp	C/T	0.000385409	0.0138765	intron-variant	RNF126	GRCh38.p7	19:651574	CTTCCGACCTCAAGG[C/T]GTGGGGCCCTCGCGG	55658
rs560390797	snp	G/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:660922	CAGATGCCCTTGGGA[G/T]CACCCGCGGGGTGGA	55658
rs560500745	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:655036	AAGCCCAGGCCAGGT[A/G]CAGCAGCTCACACCT	55658
rs560703220	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:658812	CAGGTGGCTTCAGGC[A/G]CCACCACTAGGGACT	55658
rs560763513	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653992	GGTTGCACCGGGGCT[A/G]TTCAGTCTTCGCAGG	55658
rs560776845	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:648574	ACAGCCTCAGCCGGA[A/G]GCCGCCCCTGAGCCC	55658
rs560793743	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652355	CCCATGCGCCAGGCG[C/G]TCCCTCCCCTCAAAA	55658
rs560992271	snp	A/G	0.00279162	0.0372561	intron-variant	RNF126	GRCh38.p7	19:654285	GAAAAAGTGCGGCCC[A/G]GCTCCTGGTGAGGCC	55658
rs561299758	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:651417	GGTCAACCCACACAC[C/T]CTGAACCGGCATACT	55658
rs561366454	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RNF126	GRCh38.p7	19:648004	CTGCCCTGGAACAGG[C/T]GGGACCTGCAGCGCT	55658
rs561526802	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:662326	GCAGGAAGTAGCACT[A/C]GGCACGCCCAGGCCC	55658
rs561648877	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:659850	CTCACTGCAACCTCC[A/G]CCTTCCAGGTTCAAG	55658
rs561779048	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:657745	GTCTCTCAGGCCCCC[A/G]GCCAGCCCCTCCAGG	55658
rs561789937	snp	A/C	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:661953	CCTCAGTTTCCCCAT[A/C]TATAAAGCACGGGTG	55658
rs561793179	snp	C/T	0	0	intron-variant	RNF126	GRCh38.p7	19:653278	GCATTTCCAGGACGC[C/T]CTGGCAGCCCCGCAC	55658
rs561804684	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:652549	TAGGGCCCCCGTGGC[C/T]CCTTCCCCGGAGGGC	55658
rs561866917	snp	A/G	0.00159617	0.0282053	intron-variant	RNF126	GRCh38.p7	19:652749	CTCGGCGGGGCGGAC[A/G]CCAGCACAGCCCACA	55658
rs561981750	snp	G/T	0.000399281	0.0141238	missense	RNF126	GRCh38.p7	19:650295	CGAGCTGCTGGATGA[G/T]CCTGGAAAAGAGAGC	55658
rs561984422	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:651159	GCAGGGCCCAGCGAC[A/G]GCTCCCCCAGGCTCT	55658
rs562018955	snp	A/C	0.000798403	0.0199641	downstream-variant-500B	RNF126	GRCh38.p7	19:647407	GCCGGCCCTGGGTGC[A/C]AAGCCCTGCAGGAGG	55658
rs562228298	in-del	-/AGG	0.00199481	0.0315187	intron-variant	RNF126	GRCh38.p7	19:659249	GCCGCCGCAGGGACC[-/AGG]AGAAGACAGGGTGGG	55658
rs562255750	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	RNF126	GRCh38.p7	19:647150	CGCCTTGCCAGCTGT[A/G]CCCGAGCTGGCTGCA	55658
rs562342161	snp	C/T			upstream-variant-2KB	RNF126	GRCh38.p7	19:664318	AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACCG	55658
rs562531393	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	RNF126	GRCh38.p7	19:663355	GGGCGGGGCTCCAAG[A/C]GGGGGCGGGGCTTCC	55658
rs562596864	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:649185	GAATGGGGGAATGGG[C/T]GGAGGCCCGCGCTCC	55658
rs562812201	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF126	GRCh38.p7	19:664194	GGACTAGAGGCACCC[A/G]CCACCACACCGGCTA	55658
rs562923821	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:659576	CTGGGGGCTCAGTGC[A/C]CTCAGCAGCTCTCGC	55658
rs563082067	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RNF126	GRCh38.p7	19:664756	AAGTGATTCTCCTGC[C/T]TCAGGCTCCCGAGTT	55658
rs563134103	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:654967	AGTGAGACTCCGTAT[C/T]GGGAAAAAAAAAAGT	55658
rs563199499	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:655505	AAAAAGAAAAGTGGG[A/G]GGGGAAAGGACGTGT	55658
rs563239705	snp	C/T	5.29591e-05	0.00514556	intron-variant	RNF126	GRCh38.p7	19:651953	AAAGCAAGACGGGCC[C/T]TGCTGGGTGCCGGGT	55658
rs563300225	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:652032	GCTGGTGTGAGATGC[C/T]TCGGTGGAAGTTTCG	55658
rs563431382	snp	G/T	0.00273199	0.0368582	intron-variant	RNF126	GRCh38.p7	19:648354	CGGGGTGGGGGGGCG[G/T]GTGGGCGGGGCACTC	55658

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