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

RNF216

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs77653203	snp	C/T	0.157972	0.232445	intron-variant	RNF216	GRCh38.p7	7:5687866	CAGAGATCATGATCT[C/T]ACCATTTTACAGATG	54476
rs77682118	snp	C/T	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5632861	GGATCCAATGAGTAC[C/T]ATGACGAAGCACACG	54476
rs77804903	snp	C/T	0.0138799	0.0821421	intron-variant	RNF216	GRCh38.p7	7:5751657	GTCTCCCTGTCCCAG[C/T]CTGACAAGAAAAGTA	54476
rs77858769	snp	G/T	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5644310	CCTCAATGTATACTG[G/T]TGTCATTTTTTCTAT	54476
rs77880241	snp	A/C	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5649400	GGAAAAAAAAAAAAG[A/C]CAGAAAGAAAGGGAG	54476
rs77881880	snp	C/G	0.241121	0.271662	intron-variant	RNF216	GRCh38.p7	7:5770717	ACAGTAGGAGATATT[C/G]TATTACTATTAAGTT	54476
rs77889305	in-del	-/TTT			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674045	TCAATTTTTTTTTTT[-/TTT]ACGACGGAGTCTTGC	54476
rs77900039	snp	A/G	0.039522	0.134904	intron-variant	RNF216	GRCh38.p7	7:5634205	GCCTCCTGTGACCAT[A/G]GGGGAAGAACGGGTG	54476
rs77901409	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5720296	TACTCAACGTGAAGA[C/T]CATGAAGATAAAGAC	54476
rs77905977	snp	G/T	0.0663309	0.169604	intron-variant	RNF216	GRCh38.p7	7:5650092	TTGAATGTAGGAATG[G/T]GTCATCTCTATGAAG	54476
rs77906604	snp	G/T	0	0	intron-variant	RNF216	GRCh38.p7	7:5644843	TTTTTTTTTTTTTTT[G/T]AAACGGAGTCTTGCT	54476
rs77907839	snp	C/T	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5682601	TAGTAGAGACGGGGT[C/T]TCTCCATCTTGGTCA	54476
rs77952034	snp	C/T	0.000514479	0.0160304	intron-variant	RNF216	GRCh38.p7	7:5623214	TAGTGGAGAAAAACA[C/T]TAAACCAACCTCAAT	54476
rs78016235	snp	A/T	0.110167	0.207236	intron-variant	RNF216	GRCh38.p7	7:5771320	TAGAAGATAACACAA[A/T]ATCTCCACAATCTTA	54476
rs78027198	snp	C/G	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5682609	ACGGGGTTTCTCCAT[C/G]TTGGTCAGGCTGGTC	54476
rs78032417	snp	C/T	0.0402882	0.136092	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668949	CTTCACTCATCCCCA[C/T]AGGGCTCTTATCCAG	54476
rs78061096	snp	C/G	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5709745	ATGTGTGCCCTCAGG[C/G]TTTTATTTTTTAAAT	54476
rs78083196	snp	A/T	0.0146672	0.084371	intron-variant	RNF216	GRCh38.p7	7:5749697	TCCTAAAGTGCTGTG[A/T]GTTCAAAGATGTATA	54476
rs78111716	snp	A/G	0.0111196	0.0737302	intron-variant	RNF216	GRCh38.p7	7:5655766	TTCTAAACAGTGTAA[A/G]TTTTACTAAATTGTA	54476
rs78124903	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5748304	ACCTCATTTTAATGC[C/T]GAAACTCTACCCCAG	54476
rs78196589	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5719057	ATAATGTTATTAATA[A/T]TATTAAGAACCAAGA	54476
rs78201006	snp	A/G	0.030278	0.119257	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671506	CAATCTGATAGCCTT[A/G]TAAGAAGGACAGAGA	54476
rs78222121	snp	A/C	0.0123036	0.0774623	intron-variant	RNF216	GRCh38.p7	7:5655671	GAAACCCACAATTAA[A/C]ATAAGGCAAGCAAAC	54476
rs78254837	snp	A/T	0	0	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5621190	TTTTTTTTTTTTTTT[A/T]AAAGATAGAGTTTTG	54476
rs78299955	snp	A/G	0.118584	0.212673	intron-variant	RNF216	GRCh38.p7	7:5644424	ATTTGTATTTCTGTA[A/G]TGACTAATGACGTTC	54476
rs78324415	snp	A/G	0.0189856	0.0955633	intron-variant	RNF216	GRCh38.p7	7:5691726	GCAGGGAGTCCATCA[A/G]TACTAACTCTAGACA	54476
rs78336098	snp	G/T	0	0	intron-variant	RNF216	GRCh38.p7	7:5773259	AGATTTTTTTTTTTT[G/T]TGAGACAGAGTCTCC	54476
rs78340435	snp	C/G	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5629613	GCGGGCGGATCACGA[C/G]GTCAGGAGTTTGAGA	54476
rs78364925	snp	A/G	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5740906	TTTTTTTTTTGCAAT[A/G]AAAAAAAAAAAAGAA	54476
rs78369267	snp	A/G	0.0759472	0.179459	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754373	TCACTATGTTCCTAT[A/G]CTGGCCTTGAACTCC	54476
rs78387970	snp	C/G	0.000658751	0.0181367	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741379	AGAGCAGCTGACTCT[C/G]CTAGATTTGATAACA	54476
rs78417305	snp	A/C	0	0	intron-variant	RNF216	GRCh38.p7	7:5762710	AACAAACAAACAAAC[A/C]AAAAAAAAATTAAAA	54476
rs78442038	snp	A/G	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5653625	AAAAAAAAAAAAAAA[A/G]AATTAAAAAAAAATG	54476
rs78442575	snp	C/G	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5638833	AAGATGGGGGTCTCA[C/G]TATGTTGCCCAGGCT	54476
rs78459020	snp	A/T	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5742457	TGTTCAAAAAACATA[A/T]AAAAAAATCTAAATC	54476
rs78466492	snp	A/G	0.0463947	0.145069	intron-variant	RNF216	GRCh38.p7	7:5705368	ACCAGACACGCCTGT[A/G]AGACCTCTGGCTTTC	54476
rs78480370	snp	A/G	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5649387	CTCCGTCTCCAAAGG[A/G]AAAAAAAAAAAGACA	54476
rs78521164	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5705293	AAGTAATCTCTCCTG[A/G]ATCTTTTGGATTCCA	54476
rs78524012	snp	A/T	0.0111196	0.0737302	intron-variant	RNF216	GRCh38.p7	7:5691425	TACAAGAGCAGGAAC[A/T]GATGAATGCGTAAGT	54476
rs78554265	snp	G/T	0.108048	0.20579	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739461	CTAAAGACTAGAAAA[G/T]GGCTGTGAAGCAGGT	54476
rs78558809	snp	C/G	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5766656	TGAGAAAATAAATTT[C/G]TTTTAAATGTCACCC	54476
rs78589862	snp	A/G	0.0410537	0.137264	intron-variant	RNF216	GRCh38.p7	7:5761399	GCTAACAAAGAAATG[A/G]GCTAAGGGTATTAAC	54476
rs78623933	snp	A/G	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5688946	CTGAATGAGAGAAGC[A/G]GGAAAAATATTCACA	54476
rs78640618	snp	A/T	0.5	0	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768169	GATTAAAAAAAAAAT[A/T]ACCAGGTGCGGTAGC	54476
rs78648247	in-del	-/AAAA			intron-variant	RNF216	GRCh38.p7	7:5689376	TTAAAAAAAAAAAAA[-/AAAA]GAAAGAAGAAGAAAA	54476
rs78664724	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5689279	AGTTTGTGAGGTATA[A/G]GAAAAGTGACAGAAG	54476
rs78675897	snp	A/C	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5629198	AGACTCTGTCTCAAA[A/C]AAAAAAAAAAAAAAG	54476
rs78679911	snp	A/C	0.5	0	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712473	GCGAGAATCCACCTC[A/C]AAAAAAAAAAAAGAA	54476
rs78700718	in-del	-/CTT			intron-variant	RNF216	GRCh38.p7	7:5759632	GGAGTCATTTTTCTT[-/CTT]CTTTTTTTTTTTTTT	54476
rs78708455	snp	C/T	0.0232847	0.105357	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672875	AGCACACTCCCAGGA[C/T]AATGCTGAGGAGCCC	54476
rs78714602	snp	C/T	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5688347	CAAGGGGCTGCTCTA[C/T]TTCAGACAAACCGCA	54476
rs78757243	snp	C/T	0.0298908	0.118541	intron-variant	RNF216	GRCh38.p7	7:5688193	AAAGCATTTCAAAAA[C/T]GATTAGTCTTCTTTC	54476
rs78882576	snp	A/C	0.0766824	0.180169	intron-variant	RNF216	GRCh38.p7	7:5638435	AATTAAGAGGAACTC[A/C]CAGATCAAGTACACG	54476
rs78890032	snp	C/G	0.046775	0.145601	intron-variant	RNF216	GRCh38.p7	7:5653781	GGAAGTGAGGCCTGA[C/G]ATCCAAAGGACGAGT	54476
rs78901221	snp	C/T	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5736648	AGGAGCGCCTCTTCC[C/T]GGCCACCATCCTGTC	54476
rs78960176	snp	C/G	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5759067	CAATCCGTTCTGGTT[C/G]CAACAGTGAGTTCTT	54476
rs78978127	snp	A/C	0.00795532	0.062565	intron-variant	RNF216	GRCh38.p7	7:5707445	GTGTTTGTTAGTGTA[A/C]AGGAACGCAACTGAT	54476
rs78983013	snp	C/T	0.0111196	0.0737302	intron-variant	RNF216	GRCh38.p7	7:5693519	GAAGCTCCAAGACAT[C/T]TGAGGAAGGAAAGAG	54476
rs79018348	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5771172	GTGGAAAACATGACC[A/T]TTCTACTATATGATG	54476
rs79030488	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5661799	GACAATGAGACTCTG[C/T]TCAAACAAAAACAAA	54476
rs79030595	snp	C/T	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5625615	GATTTCCCCACACAA[C/T]TGTTTGTGAACCGCA	54476
rs79032146	snp	C/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5719294	ATGGAAGGACTGCTT[C/G]AGCCCAGGAGGTAGG	54476
rs79033023	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754161	GTGTGTGTGTGTGTG[C/T]GCGCATTTGTCTGGG	54476
rs79113431	snp	A/G	0.0275645	0.114116	intron-variant	RNF216	GRCh38.p7	7:5775148	GAGCTGTTATTCACC[A/G]TGGCCATAGAACCAG	54476
rs79117988	in-del	-/AA			intron-variant	RNF216	GRCh38.p7	7:5764224	TTAAAAAAAAAAAAA[-/AA]CAGATAAGTATCCAT	54476
rs79123269	snp	A/G	0.0217236	0.101931	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712008	CCTCTTCTTTGTGCT[A/G]GCTCTTATCAGGAAA	54476
rs79134956	snp	A/G	0.0217236	0.101931	intron-variant	RNF216	GRCh38.p7	7:5703265	AAGGTCTTCCCTGAT[A/G]GTAGGAACAAGTGGC	54476
rs79150166	snp	G/T	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5655874	TGAATGGTTTTTTTT[G/T]GAGCCAGGGTCTCAC	54476
rs79153839	snp	G/T	0.0663309	0.169604	intron-variant	RNF216	GRCh38.p7	7:5651116	CCTGCTTGGCAAGTT[G/T]TCTATTTCCCACTTT	54476
rs79180634	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5690675	ACAGAAGAGCAAACA[A/G]AAGTCCACAAAGGCA	54476
rs79181066	snp	C/G	0.0162398	0.0886349	intron-variant	RNF216	GRCh38.p7	7:5738271	CCACTCTGGCTCCCA[C/G]GCTGGAGTGCAGTAG	54476
rs79214201	snp	C/G	0.0352966	0.128072	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713567	AGGTAAGAGACTTCA[C/G]AGCCATTCAGGTTCA	54476
rs79215819	snp	A/T	0.078151	0.181571	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620221	GACAGATCATGCACA[A/T]TTTTTTCAGTTTTTA	54476
rs79247182	snp	C/T	0.153	0.230415	intron-variant	RNF216	GRCh38.p7	7:5749104	TTTTGGTAAGTAAGA[C/T]CATTTGGAAAACAGC	54476
rs79260236	snp	A/G	0	0	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768311	AAAAAAAAAAAAAAG[A/G]CTGGGTCCAGTAGTG	54476
rs79267883	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5744462	GGAAGGAAAACAAGG[A/G]AGGGAAGGGAAGGAG	54476
rs79291391	snp	A/T	0.0193772	0.0965046	intron-variant	RNF216	GRCh38.p7	7:5650255	ATATATCACATTTGG[A/T]TGTTCTGCTCTTATC	54476
rs79333925	snp	G/T	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5718562	ACCCTTTTTTTTTTT[G/T]TTGAAACTGAGTCTT	54476
rs79368767	snp	A/T	0	0	intron-variant	RNF216	GRCh38.p7	7:5779674	AAAAAAAAAAAAAAA[A/T]AAAAGTTAGCCGAGC	54476
rs79396662	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713622	ATGCACCTAGAGTCA[A/G]ACTCACTGGTCTATA	54476
rs79433846	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5643716	TTAAACCACTCTAAC[A/G]TATACAATTCAGGGA	54476
rs79503824	snp	A/C/G	0.07181	0.176533	intron-variant	RNF216	GRCh38.p7	7:5703574	AACAGCAAATGCTAC[A/C/G]AAGAATAGGATGGGA	54476
rs79505983	snp	C/T	0.0263992	0.111815	intron-variant	RNF216	GRCh38.p7	7:5765037	GACCAACCCACTGCA[C/T]TCCAGCCTAGGAAAC	54476
rs79538028	snp	C/T	0.17461	0.238362	intron-variant	RNF216	GRCh38.p7	7:5774417	GCACTCCAGCATAGG[C/T]GGCAGAGGGAGAACC	54476
rs79603945	snp	A/T	0.114738	0.210248	intron-variant	RNF216	GRCh38.p7	7:5699916	ACACTGAGGAATAAA[A/T]GGCCTTTTACGTTCT	54476
rs79604920	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5649015	ATATAAGAAAAAAAG[A/G]TTTTATGGGTGAAAT	54476
rs79645573	snp	C/G	0.046775	0.145601	intron-variant	RNF216	GRCh38.p7	7:5623708	TGAGGAGCTGGGATC[C/G]CAGATGTGTGCCAAC	54476
rs79658612	snp	A/G	0.0655868	0.168795	intron-variant	RNF216	GRCh38.p7	7:5758671	TGTGGGACCTCTTGC[A/G]TCTTTCTTTTGGCCA	54476
rs79707037	snp	A/G	0.0744748	0.178019	intron-variant	RNF216	GRCh38.p7	7:5751465	CAAACCTAAACCTGG[A/G]AAGTTCATTTGATCT	54476
rs79732911	snp	C/G	0.0168055	0.0901129	intron-variant	RNF216	GRCh38.p7	7:5685802	AAAGCCCCATTAATC[C/G]TCATGCCTTGTAATT	54476
rs79738622	snp	A/T	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5690938	ACCTACAGATGAGTC[A/T]ACTTGGACCCTGTGG	54476
rs79750983	in-del	-/GCT			intron-variant	RNF216	GRCh38.p7	7:5719834	GTGGCCAATGCAGCT[-/GCT]TTGTGGCTCAGTTGC	54476
rs79760679	snp	A/G	0.11963	0.213316	intron-variant	RNF216	GRCh38.p7	7:5659335	TAACTGACACTAGGG[A/G]CCTAGTCAGAGGATG	54476
rs79767165	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667245	TTGTTTTATAAAACT[A/G]TTTCTGTTCCACCTA	54476
rs79767547	snp	C/T	0.123105	0.215401	intron-variant	RNF216	GRCh38.p7	7:5687759	GAGAAGATAAGTGAA[C/T]CCACTAGCATTTCCA	54476
rs79768350	snp	A/C	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5643094	AGAAAAAAAGGCTCT[A/C]CTAAAATGGACAGAG	54476
rs79807001	snp	A/C	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5779828	AGCCAGACTCCGCCT[A/C]AAAAAAAAAAAAAAA	54476
rs79810024	snp	G/T	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5651241	TCTCTTTTTTTTTTT[G/T]GAGTTGGAGTCTCGC	54476
rs79827154	snp	G/T	0.5	0	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666833	TTTTTTTTTTTTTTT[G/T]AGACAGGGTCTCATT	54476
rs79831858	snp	C/T	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5649976	ACACACCGTTCTACT[C/T]GAACGACATGCAGAT	54476
rs79846359	snp	C/G	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5755390	GAATAACACAGCATG[C/G]TCTATAAATCAAGTG	54476
rs79890547	snp	G/T	0.155656	0.231515	intron-variant	RNF216	GRCh38.p7	7:5760145	ATTTAACAGGAAATT[G/T]CACAAACATGTAAGA	54476
rs79922004	snp	C/T	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5638162	ACTTGGGTCTGTGAC[C/T]CCAGCAATCCATACT	54476
rs79931409	snp	A/C	0.0327778	0.123752	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621867	GCTGACTCCATGAGA[A/C]GGGAAGTGACCTTCA	54476
rs79941162	snp	C/T	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5779049	CCATTCCCAACTATG[C/T]TCTATTATCTTTAAC	54476
rs80007613	snp	G/T	0.0228947	0.104514	intron-variant	RNF216	GRCh38.p7	7:5748722	CTATTAGTAGTTAAG[G/T]AGTTATTAAGTAGTA	54476
rs80019780	snp	A/C	0.118933	0.212888	intron-variant	RNF216	GRCh38.p7	7:5635244	TGAAGAAACCGAGGT[A/C]AGTTTTGATGACAGA	54476
rs80041347	snp	C/G	0.0205511	0.0992634	intron-variant	RNF216	GRCh38.p7	7:5644038	TCATTCCTTTTTATG[C/G]TTGGATAATATTCCA	54476
rs80061249	snp	C/T	0.110167	0.207236	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676465	ATCTGTGAGAACTGT[C/T]GCTGGGGAACCCCAC	54476
rs80095848	snp	C/T	0.0168055	0.0901129	intron-variant	RNF216	GRCh38.p7	7:5774389	GCTGCAAGTAAGCTA[C/T]GATAGCACCATTGCA	54476
rs80115244	snp	A/G	0	0	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674480	CTTAAAAAAAAAAAA[A/G]GGCCAGGTGTGGTGG	54476
rs80126040	snp	A/T	0	0	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768167	TTGATTAAAAAAAAA[A/T]TTACCAGGTGCGGTA	54476
rs80161004	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5660957	GGTTTTTTTTTTTTT[G/T]TTTTTTTTTTTGAAA	54476
rs80173448	snp	A/G	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5629461	GAAGATCCTGTCTCA[A/G]AAAAAAAAAAGTGAA	54476
rs80188632	snp	C/G	0.0225045	0.103662	intron-variant	RNF216	GRCh38.p7	7:5776294	CACTAGTGTAATAAA[C/G]AGACTATAGCCGGGC	54476
rs80189939	snp	C/T	0.0244538	0.107838	intron-variant	RNF216	GRCh38.p7	7:5693281	AGATACCATATGGTC[C/T]GCAAAGCCTGAAATA	54476
rs80225185	snp	A/C	0.0158469	0.0875917	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676745	AACAACTGGGAGAGA[A/C]AGAAAACTCCTAAAC	54476
rs80228863	snp	C/T	0.095934	0.196885	intron-variant	RNF216	GRCh38.p7	7:5659862	ACACCTGTACTTTTT[C/T]TGTTAAGAAGAAGAG	54476
rs80256450	snp	C/T	0.039522	0.134904	intron-variant	RNF216	GRCh38.p7	7:5634249	ATTGCACTTTTCCTC[C/T]CCTTAGAAAGCTGAC	54476
rs80313044	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5707883	GGCGCACGCAACCAC[A/C]CCCAGCTAAATTTTT	54476
rs80336171	snp	A/G	0.093417	0.194889	intron-variant	RNF216	GRCh38.p7	7:5701478	GGCAGCTATTACTTC[A/G]TGACACAAAGTGCCA	54476
rs111230722	snp	A/G	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5748928	GATCTGCTTCTCTGT[A/G]TCTCCGTGTCTATAT	54476
rs111230842	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5727480	TGGTGGCAACCCAGT[A/G]CTTTAGGAGGTGGAG	54476
rs111244673	snp	A/G	0.0185938	0.0946107	intron-variant	RNF216	GRCh38.p7	7:5686913	TGCTGCTGCTGATCT[A/G]ACAGGAGGCAGAGCT	54476
rs111272689	in-del	-/T	0.5	0	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674033	CTGGATAATTTTCAA[-/T]TTTTTTTTTTTTTTA	54476
rs111311689	snp	G/T	0.0178098	0.0926698	intron-variant	RNF216	GRCh38.p7	7:5661078	CCAAGTAGCTGGAAT[G/T]ACAGGTATGCACCAC	54476
rs111349765	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768718	CCAGGCTGGAGTGCA[A/G]TGGCTCGATCTTGGC	54476
rs111353406	snp	A/G	0.117537	0.212022	intron-variant	RNF216	GRCh38.p7	7:5736171	CTCTGATGCCCAGCC[A/G]AAGCTGGACTGTACT	54476
rs111377420	snp	A/G	0.00953873	0.0683987	intron-variant	RNF216	GRCh38.p7	7:5645736	GCTGGGACTACAGGC[A/G]CCCGCCACCACATCC	54476
rs111435276	snp	C/T	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5759540	ACAAAACATACAATA[C/T]ATAACGCATGTGTTG	54476
rs111446120	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5761653	TAGCTGGGCGTGGTG[C/G]CACGTGCCTGTAATC	54476
rs111520255	in-del	-/T	0.00795532	0.062565	intron-variant	RNF216	GRCh38.p7	7:5641480	ATGATCACTTATGGC[-/T]TTTTTTGTGACATTA	54476
rs111578857	snp	C/T	0.0185938	0.0946107	intron-variant	RNF216	GRCh38.p7	7:5725172	TCCTAAAAATTTTGA[C/T]GTGCTGAGAAAATAG	54476
rs111579094	in-del	-/T/TT	0.126219	0.217206	intron-variant	RNF216	GRCh38.p7	7:5648108	AAGCCTTTAGCTCTA[-/T/TT]TTTTTTTTTTTTCTT	54476
rs111595620	snp	A/C	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5745206	AAAGACAATAACTTA[A/C]CAACTAAGAGGTCAA	54476
rs111617382	snp	A/G	0.00199481	0.0315187	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669065	AGAGAGTATTTCAAC[A/G]CAGGCAGGTGGCTAC	54476
rs111618510	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754039	TAAAAGAAGAGAAGA[A/G]GAAAGAAACGAAATG	54476
rs111650998	snp	C/T	0.0205511	0.0992634	intron-variant	RNF216	GRCh38.p7	7:5628302	TTTCACCCAAAATGA[C/T]GGCACTCAGCTACAA	54476
rs111676958	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5756096	GGGGGCAGTTTCCCC[C/G]ATTCTGCTCTCGTGA	54476
rs111724189	snp	C/G	0.0178098	0.0926698	intron-variant	RNF216	GRCh38.p7	7:5661154	CACATTGACCAGGCT[C/G]GTCTTGAATTCCTGG	54476
rs111727479	snp	G/T	0.135825	0.222405	intron-variant	RNF216	GRCh38.p7	7:5642222	GTTCTGTTTTGTTTT[G/T]TTTTTTTTGAGACAG	54476
rs111739322	in-del	-/A	0.5	0	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782352	CAACCCTCCATCTCG[-/A]AAAAAAAAAAAAGTA	54476
rs111743612	snp	A/G	0.0111196	0.0737302	intron-variant	RNF216	GRCh38.p7	7:5689783	GCGTGGCAAAATTCC[A/G]TCTCTACTAAAAATG	54476
rs111755769	snp	C/T	0.0341408	0.126114	intron-variant	RNF216	GRCh38.p7	7:5637822	CTGGGATTACAGGCA[C/T]GAGCCACTGCACCAG	54476
rs111766771	in-del	-/T	0	0	intron-variant	RNF216	GRCh38.p7	7:5750330	TTCCTAGCAGAGACA[-/T]TTTTTTAAAGACCAA	54476
rs111830472	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5635249	AAACCGAGGTCAGTT[C/T]TGATGACAGATCAAT	54476
rs111875023	snp	C/G	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5765025	ACAGTAAGCTATGAC[C/G]AACCCACTGCACTCC	54476
rs111942365	snp	A/G	0.138848	0.223931	RNF216	7	allele_origin=G(germline)/A(germline)	7:5730769	ATTTATAATGATTCT[A/G]TCTTCTCTCTTTGGA	54476
rs111954482	snp	C/T	0.0325976	0.123435	intron-variant	RNF216	GRCh38.p7	7:5642215	ACTCAAGGTTCTGTT[C/T]TGTTTTTTTTTTTTT	54476
rs111981961	snp	C/T	0.0111196	0.0737302	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673520	GAACAGCAAAGCTGA[C/T]CTGTCACGTGGGGCA	54476
rs111993386	snp	A/G	0.0232847	0.105357	intron-variant	RNF216	GRCh38.p7	7:5637742	ATGGAGTTTTGCCAT[A/G]TTTCCAAAGCTGGTC	54476
rs112035896	snp	C/T	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5770103	TGTAGTCCCACCACT[C/T]TGGGAGGCTGAGGCA	54476
rs112062396	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5658634	TGCACTCCAGTCTGG[A/G]TGACAGAGAGAGACT	54476
rs112068683	snp	A/G	0.0178098	0.0926698	intron-variant	RNF216	GRCh38.p7	7:5648184	TGATCTCGGCTCACC[A/G]TAACCTCTGCCCCAT	54476
rs112075956	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768762	CGCCTCCCGGGTTTA[C/T]GCCATTCTCCTGCCT	54476
rs112080762	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5627737	GGCGACAGAGGGAGA[C/G]TCTGTCTAAAAAAAA	54476
rs112082729	snp	C/T	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5749862	ATGAGACTGAATTGA[C/T]AAAAGAAGAATCATG	54476
rs112099010	snp	C/T	0.0652144	0.168387	intron-variant	RNF216	GRCh38.p7	7:5749279	CCTCAGCCTCCTGAG[C/T]AGCTGGAATTACAGG	54476
rs112105245	snp	C/T	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5744710	GGCACGGTTGGCTTA[C/T]GCCTATAATCCCAGC	54476
rs112107007	snp	C/T	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5726567	CAGGATTTAAATGTG[C/T]TCAAATCAGGGTGGG	54476
rs112124393	snp	C/G	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5750286	GATACAGCACACAAA[C/G]ACTAATGTCTGCCCT	54476
rs112195901	snp	A/G	0.0988009	0.199095	intron-variant	RNF216	GRCh38.p7	7:5733396	GAACAGAACTGTAAG[A/G]GAAGGTATCAATTTG	54476
rs112257846	snp	C/G	0.5	0	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666993	CTAATTTTTTGTACA[C/G]ACCAGGTCTTGCTAT	54476
rs112285786	snp	C/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5634659	AGACAAGCCCAGCAC[C/G]CAAATACCACTATCT	54476
rs112311344	snp	C/G	0.031825	0.122064	intron-variant	RNF216	GRCh38.p7	7:5719488	AAAAGCAAAGATGTT[C/G]TCAGAGACTACAGGG	54476
rs112321285	snp	A/G	0.0185938	0.0946107	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713898	AAACAGTGGCTTAAG[A/G]AATTTAAATTGCTCA	54476
rs112336346	in-del	-/A	0.00795532	0.062565	intron-variant	RNF216	GRCh38.p7	7:5705611	AACCATATGCCCTTT[-/A]AAAAAAAACTGCGGT	54476
rs112351486	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5779269	TCAGATTTCTCCACA[C/G]GGGCTTCAGGAGTTC	54476
rs112378505	in-del	-/AAT	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5737522	GAATGATCAATTAAA[-/AAT]AATAATAATAATAAT	54476
rs112382732	snp	A/G	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5765823	TAGCCAGGCGTGGCA[A/G]TATGTGCCTGTAATC	54476
rs112410918	snp	G/T	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5726926	GAAGGGGTACCTGAT[G/T]TGAAACGGAAGGAAG	54476
rs112457727	snp	A/T	0	0	intron-variant	RNF216	GRCh38.p7	7:5633573	GAGGGAGACTCCCTC[A/T]CAAACAAAACAAAAC	54476
rs112470603	snp	G/T	0.00199481	0.0315187	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669306	TGATCCTCTGATACC[G/T]CTATTTAGAAAAGAA	54476
rs112482800	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5705167	CTGTGTTACTGACCC[A/G]GATCACTGATCTAGG	54476
rs112503803	snp	C/T	0.5	0	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621768	AATGGGCCAGAGTGA[C/T]GCCTCAGGCACCGCT	54476
rs112521703	snp	C/G	0.155987	0.23165	intron-variant	RNF216	GRCh38.p7	7:5760239	ACTGTAGAACAGTCT[C/G]GGTGCAGTGGCTCAC	54476
rs112525451	snp	G/T	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5743727	AAACTGGTAACAACA[G/T]TTCCTCTGGGAAGTC	54476
rs112557697	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5633198	TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTTG	54476
rs112564854	snp	A/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5778756	TTTAAAATTATTATT[A/T]TTTTTGAGACGGAGT	54476
rs112567258	in-del	-/AC	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5636949	AGGAGGCAGCAGAAG[-/AC]ACAGAACGAGGAGGA	54476
rs112572995	snp	C/G	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5740251	CCTGCCTCAGCCTCC[C/G]AAGAAGTTGGGACTA	54476
rs112573422	snp	A/G	0.5	0	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674340	ATTTTCAAATTTTTA[A/G]TACAGATGGGATTTC	54476
rs112619750	snp	A/G	0.00874735	0.0655527	intron-variant	RNF216	GRCh38.p7	7:5699659	ACAGAAACAGAGCAC[A/G]AACTGTTATTTAGTT	54476
rs112627115	snp	C/G	0.135825	0.222405	intron-variant	RNF216	GRCh38.p7	7:5707942	ATGTTGGCCAGGCTG[C/G]TCTCGAACTCCAGAA	54476
rs112640762	in-del	-/A	0	0	intron-variant	RNF216	GRCh38.p7	7:5779829	GCCAGACTCCGCCTC[-/A]AAAAAAAAAAAAAAA	54476
rs112664756	snp	C/T	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5641600	GACTCAGTTTCCTCA[C/T]TTTTAAACTGTGAAA	54476
rs112669124	snp	A/G	0.00874735	0.0655527	intron-variant	RNF216	GRCh38.p7	7:5701553	GCACAAAAGCTCTAC[A/G]AGGTAGGTGCAACCG	54476
rs112724699	snp	C/G	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5632561	GCCCTCCAATCACCT[C/G]ATGTCAGGGGTTCGA	54476
rs112745079	in-del	-/A	0.288906	0.246954	intron-variant	RNF216	GRCh38.p7	7:5629195	GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	54476
rs112746518	in-del	-/T	0	0	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676022	CCCTCTTCTTTTTTC[-/T]TTTTTTTTTTGAGAC	54476
rs112806739	snp	A/C	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712629	CCTGGAAGATAAACA[A/C]AATTTTCATCATCTG	54476
rs112825145	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5627065	TCGATGCAGTTACAC[C/T]ATCAGTCCCCAAGGG	54476
rs112832463	snp	C/G	0.0178098	0.0926698	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669846	ACATCGAGCTGAGAT[C/G]GCACCACTGCACTCC	54476
rs112844102	snp	A/G	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5746095	GAACACAGGAAAAAC[A/G]GCTAACTCCCTTTTT	54476
rs112848914	snp	A/G	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5685483	TTTCCAAGACACTAA[A/G]GGATGCACACTAAAC	54476
rs112872077	snp	C/T	0.128632	0.218563	intron-variant	RNF216	GRCh38.p7	7:5639790	TTTGAGACGGAGTCT[C/T]GCTCTGTCGCCCAGG	54476
rs112894405	snp	G/T	0.00874735	0.0655527	intron-variant	RNF216	GRCh38.p7	7:5701117	ACACACACGACAGCC[G/T]CCCCCAGCACGTGGC	54476
rs112900403	snp	C/T	0.5	0	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619688	ACCTTGTCCCCTCCT[C/T]AGCTGGGCGAGGCTT	54476
rs112902264	snp	C/T	0.00835141	0.0640778	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666248	TGCAGTGGGGACACA[C/T]ATTAAGTGTAATATA	54476
rs112917749	snp	C/T			upstream-variant-2KB	RNF216	GRCh38.p7	7:5783238	GGGCTCAAGCGATTC[C/T]CCTGCCTCAGCCTCC	54476
rs112919935	snp	A/G	0.0178098	0.0926698	intron-variant	RNF216	GRCh38.p7	7:5763688	CAATCCTCCTGCCTC[A/G]GCCTCAGAGTAGCTG	54476
rs112974886	snp	C/T	0.121369	0.214369	intron-variant	RNF216	GRCh38.p7	7:5654611	AGAATCACTTGAACC[C/T]GGCAGGTGGAGGCTG	54476
rs113000216	snp	A/G	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5688064	ACCGCAAATGGAACC[A/G]AAGAGGTAATTAGAG	54476
rs113009596	snp	A/G	0.030278	0.119257	intron-variant	RNF216	GRCh38.p7	7:5772754	GAAATTTCTAGCATT[A/G]ATAACTGAAAAAAGA	54476
rs113106386	snp	A/C	0	0	intron-variant	RNF216	GRCh38.p7	7:5773776	TTTTGTCATGTTGGC[A/C]AGGCTGATCTTGAAC	54476
rs113115920	snp	A/T	0.5	0	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5621172	GAATGGGTATCTTAG[A/T]TTTTTTTTTTTTTTT	54476
rs113132759	snp	G/T	0.00159617	0.0282053	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621379	GGGACTCAAACTCCC[G/T]ACCTCAACTCATCCG	54476
rs113201084	snp	A/G	0.0107246	0.0724382	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676557	CCGTCCGTCCTGTCT[A/G]CCTGGCTGTGTGACC	54476
rs113209853	snp	C/T	0.0182019	0.0936463	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782615	AGCACATTGGGAGGC[C/T]GAGGCAGGCAGATCA	54476
rs113309670	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5710690	ACCAGTAAGCGTCCA[C/T]ATTGCTGCCACTCCC	54476
rs113312702	snp	A/T	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5755237	GAAGGGAGGGAAGGA[A/T]GAAAGGAAGGAAGGA	54476
rs113324344	snp	A/G	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5660123	CCACAGCTAAATTTT[A/G]TTATTTTATTTGTAC	54476
rs113335975	snp	C/G	0	0	intron-variant	RNF216	GRCh38.p7	7:5623182	TTGAAGGTGTTCTCT[C/G]AAAGGGATGTGGGGA	54476
rs113336701	snp	A/T	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5639338	TGGATCCCAGATAAG[A/T]GCTGCTAGCCCACCC	54476
rs113358569	snp	A/G	0.00597247	0.0543191	intron-variant	RNF216	GRCh38.p7	7:5624320	CATCAGCCTGATGGC[A/G]TTCCACAAGGAGGCC	54476
rs113441370	snp	A/T	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5648969	TAAAATTTCAATTTT[A/T]GTTTTGTTAGTGGTC	54476
rs113444315	snp	G/T	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5755210	AGGAAGGGAGGGAAG[G/T]AAGAAAGGAAGGAAG	54476
rs113590408	in-del	-/GTGTGTGT	0.5	0	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754120	TTTTTCTTTTGTGTG[-/GTGTGTGT]GTGTGTGTGTGTGTG	54476
rs113590711	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5686954	TGCTCACTCACTGGC[A/C]CAGTGCTCACCTCCT	54476
rs113592124	snp	C/T	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5776702	TGTCAGATCTGGGTT[C/T]ATCCTTTAAAAGCAC	54476
rs113595947	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5774192	TTAAATCTTGGTTTC[A/C]CATTTAGTCAATCGG	54476
rs113601006	snp	A/G	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5737191	AAGAAAAATTCTTCC[A/G]CCTTGGGATGCTGTT	54476
rs113608777	snp	C/T	0.00716266	0.059414	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754738	TACCCAATGAAAAAG[C/T]TGGTTTAGGCTGGGC	54476
rs113623972	snp	C/T	0.0178098	0.0926698	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676258	CTCAAGTGATCGGCC[C/T]GCCTTGGCCTCCCAA	54476
rs113624458	snp	C/G	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5661173	TTGAATTCCTGGCCT[C/G]AAGTGATCTGCCCAC	54476
rs113652216	snp	C/G	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5628496	AAAATTACGCTTTTA[C/G]CTAATATGTTAGACT	54476
rs113665350	snp	A/G	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5726572	TTTAAATGTGTTCAA[A/G]TCAGGGTGGGCGCGG	54476
rs113670150	in-del	-/G	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5764947	TGGTGGCACACATCT[-/G]TGATCCCAGCTACTC	54476
rs113699406	snp	G/T	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5755847	AGCATATGCTCCATT[G/T]TGGCAGATAACACTA	54476
rs113731456	in-del	-/A	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5647120	AAGTTGTGAAAGGTG[-/A]AAAAAAAAAAGGGAA	54476
rs113744768	snp	A/G	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5769441	TATTTTAAACAAAGA[A/G]GCTGGGCGTGGTGGC	54476
rs113812673	in-del	-/TTTT	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5751871	GCAACAGATTTGTAG[-/TTTT]TTTAAAAAAAACAGT	54476
rs113814442	snp	C/T	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5774606	GCTATTCTTACATTA[C/T]AAGGCTATGTTGAAA	54476
rs113814529	snp	C/T	0.170733	0.237101	intron-variant	RNF216	GRCh38.p7	7:5761332	TATTTTTAAAATACA[C/T]ATATTAAAGAGACAA	54476
rs113818799	snp	A/G	0.5	0	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674091	CTGGAGTGCAATGGC[A/G]TTATCTCGGCTCACT	54476
rs113827012	snp	A/T	0.0509478	0.151255	intron-variant	RNF216	GRCh38.p7	7:5770155	AGTTTAAGGCCAGCG[A/T]AACCCCATCAAACAA	54476
rs113827391	snp	A/G	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5736283	CCGCCACGCCTGACT[A/G]GTTTTCGTATTTTTT	54476
rs113838448	snp	C/T	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5703843	TAAGTTTCTGGAAAA[C/T]TTGACTTACACAGCT	54476
rs113848092	snp	A/C	0.00716266	0.059414	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664249	ATTTATAATTATGCC[A/C]AGTATTTTATGAGAA	54476
rs113866497	in-del	-/A	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5645776	TTGTGTTTTTAGTAG[-/A]GAAAGGTTTCACCAT	54476
rs113910899	snp	C/T	0.137867	0.223442	intron-variant	RNF216	GRCh38.p7	7:5728568	AACAGAGTGAGACTC[C/T]GTCTCAAAAAAAAAA	54476
rs113911265	snp	C/G	0.0185938	0.0946107	intron-variant	RNF216	GRCh38.p7	7:5714153	TTTTTAGCAGAGATG[C/G]GGTTTCACCATGTTG	54476
rs113925044	snp	C/T	0.5	0	intron-variant	RNF216	GRCh38.p7	7:5688477	CACATACTGAATGTG[C/T]TAAGAAATACAGAAG	54476
rs113954732	snp	A/G	0.00716266	0.059414	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674017	GGTGTGCACCACCAT[A/G]CCTGGATAATTTTCA	54476
rs113955895	in-del	-/C	0	0	intron-variant	RNF216	GRCh38.p7	7:5627785	AACCCCCTTTTTTCC[-/C]TCAGACTCTCCCCTG	54476
rs113959719	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5710592	AGTAGACTTTCCTTA[C/T]ATTTTATCTCTCCCC	54476
rs113969396	snp	C/G	0.134119	0.221521	intron-variant	RNF216	GRCh38.p7	7:5768945	GGATTACAGGCATGA[C/G]CCACTGTGCCCGGCC	54476
rs114024383	snp	C/G/T	0.016246	0.0887035	intron-variant	RNF216	GRCh38.p7	7:5742885	ACAGGTGTGGGGCAC[C/G/T]GCGCTTGGCCGATGT	54476
rs114070046	snp	A/G	0.0429648	0.14013	intron-variant	RNF216	GRCh38.p7	7:5769078	AAAATTTATGTGAAG[A/G]AGGTAAAATAGTTTA	54476
rs114098805	snp	G/T	0.0168055	0.0901129	intron-variant	RNF216	GRCh38.p7	7:5692601	GCGAGGAGAAAGGCA[G/T]AGCTGCTCAGTTCCA	54476
rs114103739	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5651597	CATGGTAAGGCTAGA[C/T]TGTTATGAGAGAAGA	54476
rs114106384	snp	A/C	0.0185938	0.0946107	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682237	TCAAATCTAGACTCC[A/C]AAAATCCCTATCTTG	54476
rs114135879	snp	C/T	0.0178098	0.0926698	intron-variant	RNF216	GRCh38.p7	7:5645267	CTTGGATGTATAGAC[C/T]CTTGTTCTTCATCAG	54476
rs114142862	snp	C/G	0.0547245	0.156101	intron-variant	RNF216	GRCh38.p7	7:5734451	ACAAATGTTTGGTTT[C/G]TGATAAATTATTGAG	54476
rs114162744	snp	A/G	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5625385	ACGGCGTCAGAGCCT[A/G]AATATCTGGCCAATT	54476
rs114197847	snp	A/C	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5720094	GATGGCTCTACGACA[A/C]TGGCCTGATTCATGC	54476
rs114205736	snp	C/T	0.00953873	0.0683987	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678430	TACGTTACCACCTCC[C/T]CAAGCGCAGAGAAAA	54476
rs114293253	snp	C/T	0.0103295	0.0711199	intron-variant	RNF216	GRCh38.p7	7:5628371	AGTTATACCTAGATA[C/T]AGGGTTAGGTGTTTC	54476
rs114348622	snp	C/G	0.0298908	0.118541	intron-variant	RNF216	GRCh38.p7	7:5661307	GGCGCCAGCATAGCT[C/G]ATGGCGGTCTCCTCA	54476
rs114370579	snp	C/T	0.0240643	0.107019	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672625	TTACATACATTCTCT[C/T]GCTGGTACCCGACGA	54476
rs114421935	snp	A/G	0.0142736	0.0832652	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671914	TGCAAGCCAAGGAGA[A/G]GGGCCTCACAAGAAA	54476
rs114429786	snp	C/T	0.0562307	0.157967	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675695	TCATGAAGCCTATAG[C/T]GCTAACTCTATTCAA	54476
rs114430978	snp	A/C	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5635122	ACCTACACATCATCT[A/C]CCTCATCTGCAAAAT	54476
rs114433773	snp	C/T	0.0376037	0.131863	intron-variant	RNF216	GRCh38.p7	7:5694811	GCCACTCTCTCAAAG[C/T]GTTCTAGGTGTTGTC	54476
rs114445688	snp	A/G	0.00993419	0.0697739	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713557	GAATCACCCCAGGTA[A/G]GAGACTTCAGAGCCA	54476
rs114446728	snp	A/C/T	3.30198e-05	0.00406313	synonymous-codon, missense, intron-variant	RNF216	GRCh38.p7	7:5741732	TCTAGACTTTTTAGG[A/C/T]CTTTCTTCTCCCAAC	54476
rs114535844	snp	A/G	0.0189856	0.0955633	intron-variant	RNF216	GRCh38.p7	7:5644367	ATCGCTTTCATTATA[A/G]TCATCCTAATAGGTG	54476
rs114541456	snp	A/C	0.0256215	0.110247	intron-variant	RNF216	GRCh38.p7	7:5739172	TGAATTTACTTAACA[A/C]CACCAAATTGTATAT	54476
rs114569385	snp	C/G	0.0295035	0.117819	intron-variant	RNF216	GRCh38.p7	7:5746808	ATAATTCAGAATTAT[C/G]ATGACCATGATGTGG	54476
rs114575980	snp	A/G	0.039522	0.134904	intron-variant	RNF216	GRCh38.p7	7:5646323	CAGTGAGCTGAGATC[A/G]CATCATTGCCACTGC	54476
rs114577155	snp	A/T	0.0185938	0.0946107	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677377	ATTGTAAGACTGGAC[A/T]ACTAATCACAGAACC	54476
rs114578673	snp	C/T	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5719215	GGGAAACCCAGGCTC[C/T]ACAAAAAAAGTTAGC	54476
rs114591107	snp	C/T	0.0146672	0.084371	intron-variant	RNF216	GRCh38.p7	7:5745380	AAGGCACCATCACAT[C/T]TAATGAAGAAACATT	54476
rs114608821	snp	A/G	0.00478085	0.0486577	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670511	ATTTTTGGTACAGTT[A/G]ATCATGTATGAAACA	54476
rs114616123	snp	A/G	0.110872	0.20771	intron-variant	RNF216	GRCh38.p7	7:5724773	GTAAACGCCTTTACT[A/G]GGTGGAAGCAACTCA	54476
rs114620667	snp	C/T	0.00931121	0.0675937	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752870	GATGACATCATCATC[C/T]AGGTCCTCTTCTTCA	54476
rs114725583	snp	C/T	0.00716266	0.059414	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677814	AGACCATTAGAGTAA[C/T]TAAATCAGAATCCAG	54476
rs114767113	snp	C/T	0.0263992	0.111815	intron-variant	RNF216	GRCh38.p7	7:5750919	GAAGATTCTGTGCAG[C/T]TGATGGCGCTTCTTG	54476
rs114768878	snp	A/G	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5729151	AATCAGGAAGGAGCA[A/G]CATTAGAATGCATCT	54476
rs114769567	snp	C/G	0.046775	0.145601	intron-variant	RNF216	GRCh38.p7	7:5643546	TATCTGTGCTCACCA[C/G]CAGCCAGTGTGTGGG	54476
rs114770651	snp	A/T	0.0240643	0.107019	intron-variant	RNF216	GRCh38.p7	7:5626705	AAAGAAAAAAGAAAG[A/T]AAGTTGTGCAGCAGG	54476
rs114771684	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666387	CTCTCTGCGAAGGTG[C/T]ATGTAAGTGAAGACT	54476
rs114788435	snp	C/T	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754529	ATTTCAGAAGACACA[C/T]GCTATGGGGGATCAT	54476
rs114789414	snp	C/G/T	0.0174357	0.0918742	intron-variant	RNF216	GRCh38.p7	7:5717542	GCAACTGGGCAGAAA[C/G/T]AGGGAATGATGTATG	54476
rs114789855	snp	C/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5624611	TGCTTAGCCCCCAAG[C/G]CTGGCCTTGGCTCCT	54476
rs114793961	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216, RNF216-IT1	GRCh38.p7	7:5662025	CAAGCTGAGGTTACA[A/G]TGGCATCTTGTGTGA	54476
rs114795496	snp	G/T	0.0189856	0.0955633	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677094	CATCTCCCTTGTTTT[G/T]AGGGCACTCTGACGT	54476
rs114795938	snp	C/T	0.0399052	0.1355	intron-variant	RNF216	GRCh38.p7	7:5655643	GACAAGACCAGACCA[C/T]GTAGCTAGATATGAA	54476
rs114798721	snp	A/C/T	0.00716266	0.059414	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619674	TTCCTGTCCTTGGAA[A/C/T]CTTGTCCCCTCCTCA	54476
rs114886123	snp	C/T	0.0410537	0.137264	intron-variant	RNF216	GRCh38.p7	7:5723773	TGAGTCAAGCAATTA[C/T]AGCCCAAAGAGCAGT	54476
rs114926721	snp	A/T	0.0111196	0.0737302	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675280	CGCTAGGTTCTGCAC[A/T]GACAAGAATTAGAAG	54476
rs114927346	snp	C/T	0.0178098	0.0926698	intron-variant	RNF216	GRCh38.p7	7:5645266	TCTTGGATGTATAGA[C/T]TCTTGTTCTTCATCA	54476
rs114937363	snp	C/T	0.113334	0.209338	intron-variant	RNF216	GRCh38.p7	7:5700191	AACCCTGCAGTGCTC[C/T]GTGCTGAGAATGCAA	54476
rs114990083	snp	A/G	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5698469	ATCATGGTTCACAGC[A/G]GCCTCGATCTTCTGG	54476
rs114996667	snp	G/T	0.0185938	0.0946107	intron-variant	RNF216	GRCh38.p7	7:5649771	CTCTTGGAGGACAGT[G/T]TATTACTTTAAGCCT	54476
rs115002944	snp	G/T	0.146314	0.227484	intron-variant	RNF216	GRCh38.p7	7:5769675	GTTGCAGTAAGCTAA[G/T]ATCACACCACTGTAC	54476
rs115013101	snp	A/G	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5715316	CAACCCATTTTAGGG[A/G]CCATAAAACAATGAT	54476
rs115087172	snp	C/T	0.00835141	0.0640778	intron-variant	RNF216	GRCh38.p7	7:5742533	TTTTCCCTGTAAGAC[C/T]GGCAAACTTTTAAAT	54476
rs115094613	snp	C/T	0.0103295	0.0711199	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673619	TCTGCAAGGAATTTC[C/T]CCATTTGGCTAGATC	54476
rs115131945	snp	A/G	0.00993419	0.0697739	intron-variant	RNF216	GRCh38.p7	7:5646994	GTACGTAGTCTTCTA[A/G]ATCTGTCTTGGCTTG	54476
rs115133829	snp	C/T	0.0168055	0.0901129	intron-variant	RNF216	GRCh38.p7	7:5628758	ACTCCTGGGCTCAAG[C/T]GATGCACCCAACCTT	54476
rs115154308	snp	A/G	0.0146672	0.084371	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676409	CTTAAAAGTGCTGAC[A/G]GCAGTTGCAAAAAGT	54476
rs115202209	snp	C/T	0.00244648	0.0348892	intron-variant	RNF216	GRCh38.p7	7:5721185	CACCTAGAAGATATA[C/T]GACAATGCAAAAGCA	54476
rs115218523	snp	A/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5747957	CCTGACCCTTAAGGT[A/T]AAGGAAACAAAAATC	54476
rs115221976	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753116	CCTCAAGCAGCCCGT[A/G]CACTTAAGCATTAAG	54476
rs115258236	snp	C/G	0.00835141	0.0640778	intron-variant	RNF216	GRCh38.p7	7:5690000	CCCCTTATTTGCCGA[C/G]TTCACCTGTATTATA	54476
rs115265330	snp	G/T	0.00676609	0.0577691	intron-variant	RNF216	GRCh38.p7	7:5743655	GTATATGTACCCACA[G/T]GTATATACACATGGA	54476
rs115277304	snp	C/T	0.0263992	0.111815	intron-variant	RNF216	GRCh38.p7	7:5771101	GTGAGCCACCACACC[C/T]GGCCCCAGATTCAGT	54476
rs115367522	snp	C/T	0.00398564	0.0444627	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670623	AGCATGCTTAATCTC[C/T]ACCCCTACTGCTTCA	54476
rs115478103	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5766384	CTCCAAATTCCTATA[C/T]TGAAGCTCTGACCTC	54476
rs115486451	snp	C/T	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5719934	ATGAAGACTTCATTT[C/T]ATTACACAGAATATT	54476
rs115487772	snp	A/G	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5700458	CTCTCCCTTGATGAG[A/G]CCACAGACACAGAAA	54476
rs115497536	snp	C/T	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5660099	AGCTCGGACTATGAA[C/T]ACGTGCCACCACAGC	54476
rs115516157	snp	G/T	0.0182019	0.0936463	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672787	GATGGATATGAGGGA[G/T]GACTCAAGATAGGAT	54476
rs115558824	snp	C/G	0.00993419	0.0697739	intron-variant	RNF216	GRCh38.p7	7:5695649	AGAGATGACAGAATG[C/G]AAAGTTGTCATTTGT	54476
rs115560679	snp	C/T	0.0185938	0.0946107	intron-variant	RNF216	GRCh38.p7	7:5738167	GGGAAAGAGTATATT[C/T]TTCATTTTATATTCT	54476
rs115564463	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5746227	TACCAAGGTTAGGCT[A/G]CACTGTGAGAGAGCA	54476
rs115605388	snp	A/G	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5651045	CAATGCGATACGAGC[A/G]GAAGTGAGATATATG	54476
rs115674001	snp	A/G	0.110872	0.20771	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678625	GCTTATAAGGAGGCC[A/G]GCACTCGTAGTGACA	54476
rs115712163	snp	A/T	0.046775	0.145601	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663277	GGAGGGCTCAATTCA[A/T]CCAATAAAAAAAAGT	54476
rs115714050	snp	C/T	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5714913	CCACATAATCACATA[C/T]ATCAGGTAATGTACA	54476
rs115723526	snp	C/T	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5636826	TCTCAGGTTAGAAGA[C/T]GACGATCCAACAAGA	54476
rs115737075	snp	C/G	0.00506888	0.0500874	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752898	TCATGCTGCTGAGGA[C/G]CTGGGGTGACCAGCA	54476
rs115739343	snp	C/T	0.0142736	0.0832652	intron-variant	RNF216	GRCh38.p7	7:5705555	AAAACAGACTTTGTT[C/T]TCACTCATGCTGCAC	54476
rs115742726	snp	A/G	0.117537	0.212022	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664069	GATTTCTAGGGCCTA[A/G]CACTAGATTTGAGCG	54476
rs115751510	snp	C/G	0.00636936	0.0560724	intron-variant	RNF216	GRCh38.p7	7:5658098	AGGAGAAAGAGGTGA[C/G]TCAGACAAGGATTCT	54476
rs115769502	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678508	GGTCAGGAAAATGGC[G/T]CTGGGCCCGCCTGAG	54476
rs115776482	snp	C/T	0.00438332	0.0466095	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621462	GGCCATCTTAGATCT[C/T]AGAGCCCACTTTAGT	54476
rs115855063	snp	A/G	0.0310518	0.120672	intron-variant	RNF216	GRCh38.p7	7:5653814	ACGATGAATAGGGCG[A/G]CGAAAACAGATCAAC	54476
rs115860394	snp	A/G	0.0244538	0.107838	intron-variant	RNF216	GRCh38.p7	7:5648296	TTTTTAGTAGAGACA[A/G]AGGTTTCTCCATGTT	54476
rs115911752	snp	G/T	0.0142736	0.0832652	intron-variant	RNF216	GRCh38.p7	7:5707331	TTTTTATAGTTTTCA[G/T]TGTATAAGTCTTTAC	54476
rs115994453	snp	A/G	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5703479	CTACTGTAGGAGGCT[A/G]CAGATGCCTGTTTTT	54476
rs116026198	snp	C/T	0.0111196	0.0737302	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668756	CTGTTAGGAAGTAGC[C/T]GGGGTCTGCTGTTGC	54476
rs116046323	snp	A/G	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5765220	TAATCCCAGGACTTC[A/G]GGAGGTCGAGGCCAG	54476
rs116051407	snp	A/C	0.0640965	0.167152	intron-variant, nc-transcript-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5680383	TGGTGGGCTTGTCAG[A/C]TCACTGGTTACTCAA	54476
rs116051838	snp	C/G	0.111928	0.208413	intron-variant	RNF216	GRCh38.p7	7:5716181	ACAGGCACGAGCCAC[C/G]GTGCCCGGCCACCAA	54476
rs116052988	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669170	CCAGCCTGAGAGGAA[C/T]ATGGGCGGTCGGGCT	54476
rs116059089	snp	A/G	0.00795532	0.062565	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676708	TGCCCCTATTCTTAA[A/G]GAATAATGGCATTTC	54476
rs116087055	snp	G/T	0.039522	0.134904	intron-variant	RNF216	GRCh38.p7	7:5627408	GAGCAACGTTCCAAC[G/T]GGCACCTCTCTCTGA	54476
rs116093338	snp	C/T	0.0166325	0.0896639	intron-variant	RNF216	GRCh38.p7	7:5690446	TTTGTTAAGGTTTCC[C/T]AGGTAGTATTAAAGA	54476
rs116143885	snp	C/G	0.0185938	0.0946107	intron-variant	RNF216	GRCh38.p7	7:5728996	CGGGGAGAACGCTGG[C/G]AGCTGTCAGTAGCTG	54476
rs116146801	snp	A/C	0.0535932	0.154675	intron-variant	RNF216	GRCh38.p7	7:5733666	GAAAACATTAACCAA[A/C]AAAAAAAAAAAAAGG	54476
rs116158225	snp	C/T	0.0322114	0.122752	intron-variant	RNF216	GRCh38.p7	7:5763906	AAAAAATAAAACAGA[C/T]GGCAGGGCACGACAG	54476
rs116159302	snp	A/C	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675279	ACGCTAGGTTCTGCA[A/C]AGACAAGAATTAGAA	54476
rs116178103	snp	C/T	0.00835141	0.0640778	intron-variant	RNF216	GRCh38.p7	7:5697740	GGATGCAAGGGTGCT[C/T]GCCTGGAGAAGACAG	54476
rs116333007	snp	A/G	0.0189856	0.0955633	intron-variant	RNF216	GRCh38.p7	7:5646145	TGAATATTATACTGA[A/G]AAGAGTCTAGAAATC	54476
rs116352976	snp	C/T	0.00557542	0.0525036	intron-variant	RNF216	GRCh38.p7	7:5631549	TTCAAGATTTCCTTG[C/T]CTGACATGTTTTCTC	54476
rs116391645	snp	C/T	0.0263992	0.111815	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712943	CAGTGGTTAAAAACA[C/T]AGATCCTGAGACAAC	54476
rs116399433	snp	A/G	0.00874735	0.0655527	intron-variant	RNF216	GRCh38.p7	7:5744647	CTCTACAAAACAAAC[A/G]AACAAACAAAAAACA	54476
rs116418829	snp	A/G	0.0402882	0.136092	intron-variant	RNF216	GRCh38.p7	7:5642607	GCATCACAGGTGTGT[A/G]CCACCACATCACCAC	54476
rs116477475	snp	C/T	0.0283406	0.115616	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675043	TAAAGCAAATGTCGG[C/T]ACAGAATGGCAACTG	54476
rs116486709	snp	A/G	0.0107246	0.0724382	intron-variant	RNF216	GRCh38.p7	7:5746631	CATCTTGGAGCCAAC[A/G]TCATCCCGGTCCTGA	54476
rs116546059	snp	A/G	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5685812	TAATCCTCATGCCTT[A/G]TAATTAAATATGTAT	54476
rs116547493	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5690811	CAGGGATGTACACAC[A/G]CATGTTCTGCCAGGA	54476
rs116636581	snp	C/T	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5657209	ACATGCCACAGGGCA[C/T]TACGCTGTTGCCAAT	54476
rs116643401	snp	C/T	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5762144	TACAACACAGTTAAA[C/T]TAACTAATGTTAAAT	54476
rs116646260	snp	C/T	0.00517822	0.0506191	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678328	TCTGCAATGTCAATA[C/T]ATTACCTGCGTTTCA	54476
rs116647630	snp	A/C	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5682682	AAAGGGCTGGGATAT[A/C]GGCGTGAGCCTCTGC	54476
rs116683012	snp	C/T	0.0146672	0.084371	intron-variant	RNF216	GRCh38.p7	7:5770072	TGAAAATCGGCTGGG[C/T]GTGGTGGCTCACGCC	54476
rs116702363	snp	C/T	0.0189856	0.0955633	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671870	GCACAGAAAAGACCA[C/T]GTGAGGACACAGCAC	54476
rs116704513	snp	A/G	0.0185938	0.0946107	intron-variant	RNF216	GRCh38.p7	7:5630258	GGCTGCTGGCGTCAC[A/G]GGAAGAACTACAACT	54476
rs116719191	snp	A/G	0.00636936	0.0560724	intron-variant	RNF216	GRCh38.p7	7:5626830	TTAAGGACTGAATGA[A/G]CTCAAGTATGTAAAG	54476
rs116731464	snp	C/T	0.0414363	0.137845	intron-variant	RNF216	GRCh38.p7	7:5764271	TGTGGTGAAACTATA[C/T]AGGCTATTGGACAGT	54476
rs116768517	snp	C/T	0.0260105	0.111035	intron-variant	RNF216	GRCh38.p7	7:5723370	ATAAATGCAATTGGC[C/T]GGGTGCGGTGGCTCA	54476
rs116804835	snp	C/T	0.120674	0.21395	intron-variant	RNF216	GRCh38.p7	7:5624520	CACAAGCGCTCGGCA[C/T]GGCAGCCTGTCTGCA	54476
rs116825498	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5687772	AATCCACTAGCATTT[C/T]CAAGGACCTAAGTTT	54476
rs116866342	snp	C/G	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5748918	AAGGCTATAAGATCT[C/G]CTTCTCTGTGTCTCC	54476
rs116866567	snp	C/T	0.109108	0.206518	intron-variant	RNF216	GRCh38.p7	7:5728249	CCTTAGGTTGCCTCC[C/T]GTTTTACCCTTTCAA	54476
rs116896316	snp	A/T	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5706287	CAATTAACACATTTT[A/T]AAGTGTACAGGGTCT	54476
rs116900059	snp	A/T	0.0142736	0.0832652	intron-variant	RNF216	GRCh38.p7	7:5657989	GTGCACTCTACTGAG[A/T]GAGTTACATATCGGG	54476
rs116905468	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5696906	TCTCTCCCTCCCTCC[C/T]ACTCCCTTTCAAGGA	54476
rs116912092	snp	C/T	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5746890	AGACTCCAAATTACA[C/T]GGAGAGAACGAGATT	54476
rs116924666	snp	A/G	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5751082	ATTACCCTCCTTAGA[A/G]TCCTAACGGCAGTCT	54476
rs116938992	snp	C/G	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5729913	TACGTAAGAGAGACA[C/G]TCAAAGAATCTATGG	54476
rs116952741	snp	C/G	0.0142736	0.0832652	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620084	TTTACAAAAGTCCCA[C/G]TTACATATGATACAG	54476
rs116976868	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675283	TAGGTTCTGCACAGA[C/G]AAGAATTAGAAGCCC	54476
rs117011717	snp	A/G	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5772382	AAAAAACTAGACAAG[A/G]AAGAATCTCCACAAA	54476
rs117016868	snp	G/T	0.0402882	0.136092	intron-variant	RNF216	GRCh38.p7	7:5689764	TTCAAGACAAGCCTG[G/T]CCTGCGTGGCAAAAT	54476
rs117029666	snp	A/G	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5708845	CAGGCAGCCCCTTGA[A/G]AAGCCCAAATGCTGA	54476
rs117052169	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5688591	AAAGTTAAAGGCGCA[C/T]GTATTTACCAGCTTT	54476
rs117056884	snp	C/G	0.111224	0.207945	intron-variant	RNF216	GRCh38.p7	7:5765637	TGCCTCTGAAACAAA[C/G]AAAAAGCATGAAAAA	54476
rs117075173	snp	A/T	0.0142736	0.0832652	intron-variant	RNF216	GRCh38.p7	7:5624736	CCTGAAATAACAAAC[A/T]CAATTCACACTTGGG	54476
rs117104162	snp	C/T	0.0225045	0.103662	intron-variant	RNF216	GRCh38.p7	7:5700007	ACCCAACAGCAGCTT[C/T]AGCTTAGGCTTTGCT	54476
rs117106710	snp	C/T	0.0142736	0.0832652	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670829	CTACCCGGGAGGAAC[C/T]TGTAGTGGTGGCCAT	54476
rs117107020	snp	C/T	0.0154538	0.0865337	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767009	CATTTTTCTTATCAC[C/T]TTACATGCATAACAC	54476
rs117146126	snp	C/T	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5759493	AATCACACTTCTTTT[C/T]TGTAGCTCACTTTAT	54476
rs117202272	snp	A/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5703160	CATGCAGCATGGACT[A/T]CCACTCCAGTAAATG	54476
rs117205629	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5650186	AGAAGCATCCTCTAT[C/G]ACTAAGGAAGAAGCC	54476
rs117206608	snp	C/T	0.0154538	0.0865337	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682197	CAGATTCTGTACCTA[C/T]GTGCCAGCCCACACT	54476
rs117208734	snp	A/G	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5685191	TGTACAATGTCCACC[A/G]CGGATGGGTGGGCAT	54476
rs117238116	snp	A/C	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5716524	TATTATCTTCCCTTC[A/C]ATTCTGATTCAGTGT	54476
rs117240984	snp	C/G	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5778261	ATGACTTGCTCCTTC[C/G]TTCCACTGCAGGCTC	54476
rs117255303	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5726356	GTGAGTCCCATTCTG[C/T]AGGCAAATCTTCCAT	54476
rs117289428	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5626817	ATGGGCTGCTTTGTT[A/G]AGGACTGAATGAGCT	54476
rs117312341	snp	G/T	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5708087	ATTTCTAAGTGTATC[G/T]CCTTGTGGCTGGAAA	54476
rs117322660	snp	C/T	0.0154538	0.0865337	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678378	GTTAAGGCTGACAGG[C/T]CCTGGGCAGGGAACT	54476
rs117324562	snp	A/G	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5625550	ACCAACGGACAGTTT[A/G]CAGGTTTACTTACTA	54476
rs117330906	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676781	GTGCAACCTGAGCCA[C/T]GACACAGAAAAGCCA	54476
rs117332740	snp	A/C	0.0165278	0.0893908	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620940	ACAGGGAGCATATTT[A/C]AGGTACCGAAGACAA	54476
rs117351094	snp	A/C	0.0162398	0.0886349	intron-variant	RNF216	GRCh38.p7	7:5776812	AGGCTGAGGCACAAG[A/C]ATGGCTTGAACCTGG	54476
rs117354018	snp	A/G	0.108755	0.206276	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753807	TGAGACCAGCCAGAC[A/G]AACACGGTGAAACAC	54476
rs117357552	snp	C/T	0.0154538	0.0865337	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681158	CAAGTCCTGAATCGT[C/T]TGTGGTTCTTCAGAG	54476
rs117358904	snp	A/G	0.0142736	0.0832652	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670393	TCTGATGTGCATAGA[A/G]GGGCTGCCAAAAGGA	54476
rs117366638	snp	C/T	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5636776	ATTTGCCTGACCTTC[C/T]TTTCAAACTTTATTT	54476
rs117387225	snp	A/G	0.00795532	0.062565	intron-variant	RNF216	GRCh38.p7	7:5777650	AGGAAGAACAAAGCA[A/G]ATGATGAGTTCAGAG	54476
rs117435084	snp	A/C	0.00636936	0.0560724	intron-variant	RNF216	GRCh38.p7	7:5700569	AGCTTCTGATCCCCA[A/C]AGGCTGTGACAAGCC	54476
rs117438505	snp	G/T	0.118933	0.212888	intron-variant	RNF216	GRCh38.p7	7:5629257	TGAGGCAGCAGGATC[G/T]CTTGAGGCCAGGATT	54476
rs117445130	snp	A/G	0.108402	0.206034	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767724	CTGCCTCAGCCTCCT[A/G]AGTAGTGGGGACTAC	54476
rs117469370	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5783607	CTTCTCTAAGACAGT[A/G]GAGTGTGGCTTATGG	54476
rs117479630	snp	A/C	0.0103295	0.0711199	intron-variant	RNF216	GRCh38.p7	7:5693128	TGCTACGGGTTGGCA[A/C]ACTACAGCTCACTGG	54476
rs117480862	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754706	CTGACCCAAGAAAAA[A/G]ACACACAATCTTGGT	54476
rs117484155	snp	A/G	0.0509478	0.151255	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767291	CATCCTATATTTTTT[A/G]TCTCCTGAAGGCATA	54476
rs117486357	snp	A/C	0.0494327	0.149241	intron-variant	RNF216	GRCh38.p7	7:5724570	AGAGCCACTGCTCCA[A/C]AGACTGGCTTAGGAA	54476
rs117488276	snp	C/T	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5739216	AAATGGTAAATTTTT[C/T]ATTACATATATTTTA	54476
rs117492238	snp	C/G	0.0513262	0.151752	intron-variant	RNF216	GRCh38.p7	7:5735432	AAGCTATGTTTATTG[C/G]TTAAAGAAATTAAAA	54476
rs117506427	snp	A/C	0.0146672	0.084371	intron-variant	RNF216	GRCh38.p7	7:5632837	AAGGTGTACCTATGG[A/C]TCACAGTGGGATCCA	54476
rs117513234	snp	C/T	0.0158469	0.0875917	intron-variant	RNF216	GRCh38.p7	7:5655722	ATTTGGAGCTCTCTC[C/T]GTGTAGTGTCTTTAA	54476
rs117524967	snp	G/T	0.167158	0.235875	intron-variant	RNF216	GRCh38.p7	7:5727355	ATCCTGCCTTTGCAC[G/T]TACTAATCTATGCTT	54476
rs117547683	snp	C/G	0.0948562	0.196037	intron-variant	RNF216	GRCh38.p7	7:5756308	CATAAATTACCCAGT[C/G]TCAGGCATTTCTTCC	54476
rs117572252	snp	C/T	0.110872	0.20771	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674068	GGAGTCTTGCCTTGT[C/T]GCCCAGGCTGGAGTG	54476
rs117603223	snp	A/G	0.00199481	0.0315187	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678436	ACCACCTCCCCAAGC[A/G]CAGAGAAAAATGAGA	54476
rs117636845	snp	C/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754056	AAAGAAACGAAATGA[C/T]GCACCTCATCACTGC	54476
rs117639196	snp	C/T	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5771264	ACACAAAAACAATTT[C/T]AGATAACTACACATT	54476
rs117660339	snp	C/T	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5701519	TTGACACTTTACCCA[C/T]GCTGTTTCCATTGGT	54476
rs117684214	snp	C/G	0.0283406	0.115616	intron-variant	RNF216	GRCh38.p7	7:5624228	ATGGCCATGGAACAA[C/G]CCCGAAGCCTGCTGC	54476
rs117692834	snp	C/T	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5765227	AGGACTTCGGGAGGT[C/T]GAGGCCAGTGGATTG	54476
rs117701596	snp	A/G	0.109814	0.206997	intron-variant	RNF216	GRCh38.p7	7:5773077	GAGCCACCATGCCTG[A/G]CCCCAGGTATTCCCA	54476
rs117703598	snp	A/T	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5747489	ACGTGACCCTTAGAA[A/T]GCCATTTCCAAAATG	54476
rs117704835	snp	A/G	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5709326	CTTCCTCCCAATCAC[A/G]TGGTGCTGTGCCAGG	54476
rs117744720	snp	C/T	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5698008	TCAGCTTCTCAGACA[C/T]AGGCAGCTTTTGAAA	54476
rs117811344	snp	A/T	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5685827	GTAATTAAATATGTA[A/T]GTTAAGAAGGCTGGA	54476
rs117812387	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5716409	ATCTTGCCCTGAGGT[C/T]AGACATACCTCGTTA	54476
rs117859886	snp	A/G	0.0142736	0.0832652	intron-variant	RNF216	GRCh38.p7	7:5631183	CAAAACGCAGAGCAA[A/G]GGGCTGTGTTTTGGA	54476
rs117870934	snp	A/G	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5742552	AAACTTTTAAATTAG[A/G]TAATACCAAGCATTG	54476
rs117872398	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681118	CTGGCTCTTTGAACG[C/T]CTAGCCTCTTGCTTA	54476
rs117889531	snp	A/G	0.0667028	0.170006	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667505	ATGCCCGGGAACCAG[A/G]GGAACCCCCCAGCCT	54476
rs117892683	snp	C/T	0.00874735	0.0655527	intron-variant	RNF216	GRCh38.p7	7:5654245	GGTGTAGAGATGAGT[C/T]GCCGTGCCTGGCCCT	54476
rs117897027	snp	G/T	0.00557542	0.0525036	intron-variant	RNF216	GRCh38.p7	7:5700544	GGTTTCTAGAAAGAG[G/T]GCCACTCCAAGCTTC	54476
rs117898897	snp	G/T	0.0158529	0.0876593	intron-variant	RNF216	GRCh38.p7	7:5759187	TTTTCCTTCTGTCAT[G/T]ATTGTAAGTTTCCTA	54476
rs117899626	snp	A/G	0.010732	0.0725379	intron-variant	RNF216	GRCh38.p7	7:5707660	GGAAGTGGTGACAGT[A/G]ATATCCTTGCCTTGT	54476
rs117924742	snp	A/C	0.00199481	0.0315187	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668667	ACAGAAGAATGATAA[A/C]AAGTATAGGTGGGAG	54476
rs117938627	snp	G/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5641898	ATTTGCCAGGCGTGG[G/T]AGTGCACACCTGTAA	54476
rs117980091	snp	A/G	0.0165278	0.0893908	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619783	CACCTTTCTTGCAGG[A/G]GATTCTGTGCCAAAA	54476
rs118004770	snp	C/T	0.110167	0.207236	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5780217	CATGGGTCTTCCTCA[C/T]AAGGGAAGAAACCCC	54476
rs118028406	snp	A/G	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5700132	TGTTTTCATGCTTGC[A/G]GTATTACCATAGCAA	54476
rs118031609	snp	C/T	0.0142736	0.0832652	intron-variant	RNF216	GRCh38.p7	7:5633018	AGAGTCGTGCTCTAT[C/T]GCCCAGGCTGGAGTG	54476
rs118057926	snp	C/T	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5772752	CAGAAATTTCTAGCA[C/T]TGATAACTGAAAAAA	54476
rs118058903	snp	A/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5661264	TGTTTTTCGAAGGGA[A/T]TGGGTCTCACTCTAT	54476
rs118069356	snp	A/T	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5760137	GAATTCGAATTTAAC[A/T]GGAAATTTCACAAAC	54476
rs118084971	snp	C/G	0.00795532	0.062565	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619924	ACTGGGCCTTCCGGG[C/G]CTGCTCCTGCCAGGA	54476
rs118085284	snp	C/T	0.00279162	0.0372561	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678827	TCATCAGGGAAGACA[C/T]GAGAGCTGGACTGGA	54476
rs118091325	snp	C/T	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5774120	CTCTGTATCAGGTCA[C/T]TTAACTCTCTGACAC	54476
rs118091826	snp	A/G	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5730889	TGCTTCAAATGCAAT[A/G]GTTGAAGAATATAGT	54476
rs118095970	snp	A/G	0.0329836	0.124112	intron-variant	RNF216	GRCh38.p7	7:5718501	CTTAGACAAAAAAAC[A/G]AAACCAATTCTCTAA	54476
rs118108960	snp	A/T	0.0142736	0.0832652	intron-variant	RNF216	GRCh38.p7	7:5639022	GGAGACTCCTCAGTA[A/T]AACATCTTCCTCCAC	54476
rs118120700	snp	C/T	0.0107246	0.0724382	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681486	GACCCAGTGTGCCTC[C/T]CTCTCTAGTTTATTC	54476
rs118133420	snp	A/G	0.0162398	0.0886349	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669891	TCCATCTCAAAAAAA[A/G]AGAAAGTAAGTGAGA	54476
rs118159666	snp	A/G	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5759619	ACTTAAGTTTTGGTG[A/G]AGTCATTTTTCTTCT	54476
rs118182832	snp	A/T	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5766531	TGCTTTTTCTCTCCA[A/T]CATGTGAGAACACAG	54476
rs118187626	snp	A/G	0.0178098	0.0926698	intron-variant	RNF216	GRCh38.p7	7:5642272	GCCTGGGGCACAGTG[A/G]CTCCATCTCAGCTCA	54476
rs137885195	snp	C/T	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5641036	GGTTATCAGTCTATG[C/T]AATTTCCTATATTCT	54476
rs137903337	snp	C/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5697003	AGCTCCAGGGACGGG[C/G]GTAGGGGAAGTCTCC	54476
rs137910011	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5727629	CCTAGCTACATGGGA[A/G]GCTGAGGCAGGAGGA	54476
rs137917971	snp	A/G	0.0142736	0.0832652	intron-variant	RNF216	GRCh38.p7	7:5637640	CATCCCTAACGTCCC[A/G]GGCTAAAGCAATCGC	54476
rs137938900	snp	A/G	0.00835141	0.0640778	intron-variant	RNF216	GRCh38.p7	7:5771960	CACAAGGGGCCGGGC[A/G]TGGTGGCTCACGCCT	54476
rs137964605	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673337	TTCAAGAACAGGCTC[C/G]ACAGAATGGAGTGGG	54476
rs137981401	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5746148	GGAGCTGCAAGTGTC[A/G]GAAGTCCTTCTCAGG	54476
rs137996886	snp	A/G	0.000232203	0.0107725	synonymous-codon, intron-variant	RNF216	GRCh38.p7	7:5741783	GGCAGCTGGTTTGAT[A/G]AGATTGGGTCGTGAT	54476
rs138024685	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5627224	GACAAACACACACAC[C/T]GGGCCACTCAATGGT	54476
rs138037608	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5636339	TTTATAAGACTCTTA[A/G]TTGAATGCTTTTGGC	54476
rs138052217	snp	C/T	0.0193772	0.0965046	intron-variant	RNF216	GRCh38.p7	7:5717314	GCCGAAATCGCACCA[C/T]TGCACTCTAGCCCGG	54476
rs138057859	snp	G/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5659155	CGGTGGGAGGCAGAG[G/T]CGAGTTTAGTTCCAG	54476
rs138084881	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5742035	TTAAAGCTTGAGATA[C/T]AGTTTGAATTATAAT	54476
rs138117808	snp	C/G	3.36412e-05	0.00410115	missense	RNF216	GRCh38.p7	7:5622886	GCCGCGGCTGGGGGC[C/G]AAAGTGCATGGGCAG	54476
rs138122142	snp	A/C	0.000637717	0.0178452	synonymous-codon, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711812	CACATCACTGTCCAA[A/C]AGAGCCGGAAAGCTA	54476
rs138133390	snp	A/T	0.0154538	0.0865337	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681523	GTGTTCTCAAGCCTC[A/T]AGGGCTAGGCAGGAC	54476
rs138137574	snp	C/G	0.00557542	0.0525036	intron-variant	RNF216	GRCh38.p7	7:5623564	CTCACCCTCCCGAGT[C/G]CTGGGATTGCAGATG	54476
rs138164404	snp	C/G	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5763991	GTCAGGAGTTTGAGA[C/G]CAGCCTGGCCAACAT	54476
rs138170700	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5690900	ACATTCATCATGGAA[C/T]TGCGATTTGGGGGCT	54476
rs138219600	snp	A/C	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5687827	ATCCCCTCCTTTAAT[A/C]TTCAGACAACCCAGT	54476
rs138260437	snp	A/G	0.0107246	0.0724382	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676893	GTGCATCCAGCTGGG[A/G]CACTTCAAAATGGGA	54476
rs138276508	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5686767	CCTAGGAACCAGTTT[C/T]GTGGAAGACTATTTT	54476
rs138276967	snp	G/T	0.0329836	0.124112	intron-variant	RNF216	GRCh38.p7	7:5651701	GTTGGCAGGCTGGAG[G/T]GCACTGGCGCAATCT	54476
rs138324765	snp	C/T	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5725667	CCAGTCTGGCCAACA[C/T]GGTGAAACCCTGTCT	54476
rs138328361	in-del	-/AA			intron-variant	RNF216	GRCh38.p7	7:5765953	TGAGACTCTGTCTCA[-/AA]AAAAAAAAAAAAAAG	54476
rs138332803	snp	C/T	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753259	AATCTGTTTACAAAA[C/T]TTTCTTGACTGCCAA	54476
rs138337391	snp	C/G	0.110519	0.207473	intron-variant	RNF216	GRCh38.p7	7:5734729	TTCGGGAGACTGAGG[C/G]AGGAGAATCACCTGA	54476
rs138341539	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5685877	GTATGTGAATTCTTT[A/G]TATTTGGAGCACTAT	54476
rs138412054	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5691243	AGACAAGCCACCTGA[C/T]ACCTCGCCACTCGGG	54476
rs138415635	snp	C/G	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5634000	AGTGATTAAAAAGGG[C/G]AAAAGATTCAATTTA	54476
rs138424661	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5644039	CATTCCTTTTTATGG[C/T]TGGATAATATTCCAT	54476
rs138433910	in-del	-/GGC			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678768	AAGCTGCAGAGGCTG[-/GGC]CTCCTCACACAGAAG	54476
rs138463937	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5625769	TGAGTAAGTAATTAG[A/G]TAACACATTCCCTTG	54476
rs138468116	snp	A/G	0.0142736	0.0832652	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619587	AACAGCGAGGGTAGC[A/G]GGGCCCTGGCACTGC	54476
rs138475333	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5777302	CAAAATTATTCTATG[A/C]AGCAGTAAGTATTAG	54476
rs138476221	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5651064	GTGAGATATATGTAT[A/T]TAATTCCTGTATCAC	54476
rs138509914	snp	C/T	0.000277491	0.0117758	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5730762	TACTGGGATTTATAA[C/T]GATTCTGTCTTCTCT	54476
rs138517607	snp	C/G	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5648935	GGAACTGTGAAGTTG[C/G]TATGAGATATCAAAG	54476
rs138532657	snp	A/C/G	1.64808e-05	0.00287057	missense, intron-variant	RNF216	GRCh38.p7	7:5741701	AATAGCTGCTCTTAT[A/C/G]TGATTCAAATGCTGC	54476
rs138549826	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669391	ACACACTCATTATCC[A/G]TTCTTTTCAGTGTGG	54476
rs138557303	snp	A/G	1.67237e-05	0.00289164	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752885	CAGGTCCTCTTCTTC[A/G]TGCTGCTGAGGAGCT	54476
rs138562077	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5700989	TCATTTCTTCTGAAT[A/G]TCATCCCTGAGATTC	54476
rs138562671	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665087	ACAGGCACGAACCAC[C/T]GCACCCAGCCAGGAC	54476
rs138564428	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5702426	GTTTTGTTATAATGC[A/G]TATGTATTTTTACCT	54476
rs138573381	snp	A/G	3.29527e-05	0.00405898	synonymous-codon	RNF216	GRCh38.p7	7:5641298	GCGGCAAGACATGCG[A/G]TTGCAGCCTTCAGAT	54476
rs138578369	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5655618	CTCAAAAAAAGGGGG[A/G]ACAAAAAAAGACAAG	54476
rs138603480	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5750155	TTATGTTACCAAGGC[G/T]TTGACTGGAATGCCA	54476
rs138604303	snp	A/G	0.00795532	0.062565	intron-variant	RNF216	GRCh38.p7	7:5697463	ATGATCGTGTTTAGA[A/G]GAGAAGATGAAGTGT	54476
rs138611004	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5687283	CGCCTGTAATCTCAG[C/T]TACTTGGGAGGCTGA	54476
rs138643936	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5771584	GGCAGATCACTTGAG[C/G]TCAGGAGTCTGAGAC	54476
rs138647737	snp	C/T	0.00250193	0.0352804	intron-variant	RNF216	GRCh38.p7	7:5760953	ATACAGCTGTGATAC[C/T]AAAAGAAAAAGCCAC	54476
rs138706236	snp	C/T	0.0142736	0.0832652	intron-variant	RNF216	GRCh38.p7	7:5651472	CGTGAGCTCAAGCGA[C/T]CTACCTGCCTTAGCC	54476
rs138739607	snp	A/C	0.0263992	0.111815	intron-variant	RNF216	GRCh38.p7	7:5734125	ATAGGAAGGTGGATG[A/C]CAGGGTGTGGGGCAA	54476
rs138813469	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5625910	TGATGGGTTTGGACT[A/G]AAAGGTCTCATAAGC	54476
rs138814677	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5632812	CTCCAGTGCCCCATC[A/G]CTACTCCAGAAGGTG	54476
rs138838436	snp	C/T	0.0433465	0.140692	intron-variant	RNF216	GRCh38.p7	7:5685378	TGTTGGCCTGTGTTC[C/T]CTCCTCCTCCCCACA	54476
rs138845527	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681756	CAGCTTCAACACTCC[A/G]GCTTACTGACTGGCC	54476
rs138849550	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5624510	ATCCCAAGTCCACAA[A/G]CGCTCGGCATGGCAG	54476
rs138869537	snp	A/G	0.0577344	0.159793	intron-variant	RNF216	GRCh38.p7	7:5764446	TGAAGTCAGGAGTTC[A/G]AGACCAGCCTGGTCA	54476
rs138875603	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5630845	TGAACTGATTGCCAC[A/G]CTGCAGATGAGGAAA	54476
rs138880049	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5720047	TCTTAAAAATGTAAG[C/T]GCATGGTGGTGAAGA	54476
rs138893495	snp	A/C	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5661392	TTTGTTAAAGAAATA[A/C]ATGAGACCTGCTAGG	54476
rs138928771	snp	A/G	0.0134861	0.0810011	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620184	TTTAATGAACTAATC[A/G]TTTCTTGTTTTTATA	54476
rs138944484	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5717710	AAATCCCTATGAATT[A/G]CTGCAGAGTGACTGC	54476
rs138944841	snp	A/G	0.00953873	0.0683987	intron-variant	RNF216	GRCh38.p7	7:5745803	TACTCTCGGGAGGCT[A/G]AGGCAGGATAATTGC	54476
rs138954656	snp	C/G	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5709281	TCCAGTCTTCTTTTT[C/G]CTCCCCAGAAAGATG	54476
rs139009091	snp	C/T	0.0146672	0.084371	intron-variant	RNF216	GRCh38.p7	7:5750434	GTCTTACTGTGATTA[C/T]CTTTGGTAGAAATGG	54476
rs139029849	in-del	-/A			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682051	CTGCTGCCTCTTCTC[-/A]GGGTGGGGATGATGG	54476
rs139067537	snp	A/G	0.0142736	0.0832652	intron-variant	RNF216	GRCh38.p7	7:5756597	ATGGGGTTTCCCCAT[A/G]TTGGCTAGGCTGGGT	54476
rs139104500	snp	A/G	0.0142736	0.0832652	intron-variant	RNF216	GRCh38.p7	7:5657470	TACTCAGGAGGCTGA[A/G]GCAGGAGAATAGCTT	54476
rs139161699	in-del	-/AA			intron-variant	RNF216	GRCh38.p7	7:5738708	GTGAGACTCCGTCTC[-/AA]AAAAAAAAAAAAAAA	54476
rs139183906	snp	C/T	1.7814e-05	0.00298441	synonymous-codon	RNF216	GRCh38.p7	7:5623157	CTTCTCCAGCGGGGG[C/T]CCAATGCGTTTGAAG	54476
rs139192613	in-del	-/GAGTGCTTGTAGCCA	0.478603	0.101197	intron-variant	RNF216	GRCh38.p7	7:5769906	GCCAGGCTTGGTGGC[-/GAGTGCTTGTAGCCA]GGAGGCTGAGACAGA	54476
rs139208840	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5710685	CTAGCACCAGTAAGC[A/G]TCCACATTGCTGCCA	54476
rs139209990	snp	A/G	0.0103295	0.0711199	intron-variant	RNF216	GRCh38.p7	7:5653383	ATCACGAGGTCATGA[A/G]GTCAGGAGATTGAAA	54476
rs139225554	snp	A/G	0.0185938	0.0946107	upstream-variant-2KB	RNF216	GRCh38.p7	7:5783074	TGGTGGTGCGCACCT[A/G]TAGTCCCAGCTACTC	54476
rs139230321	snp	C/T	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5647966	TTAGGCCATGACATT[C/T]ATTTGCTTAGAAGTA	54476
rs139238589	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5721968	TGCTCTGCTGCTCAC[A/G]CTGGAGTGCAGTGGC	54476
rs139288957	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681101	ACCTCAACAGCTTGT[C/T]CCTGGCTCTTTGAAC	54476
rs139296878	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5747945	CACTGTGTCTGCCCT[G/T]ACCCTTAAGGTTAAG	54476
rs139308375	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677363	GGTAAATTATCTCCA[C/T]TGTAAGACTGGACTA	54476
rs139313068	snp	C/T	0.00993419	0.0697739	intron-variant	RNF216	GRCh38.p7	7:5757106	GCAGAATCCCACCTA[C/T]GTTTATTACATTTGT	54476
rs139313183	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5706303	AAGTGTACAGGGTCT[A/G]TTAGCAAAATGTTGT	54476
rs139332013	snp	A/C	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5732228	CACTGAGGTTATGCA[A/C]ACCTTTGAAGGCTGA	54476
rs139337390	snp	A/G	1.65883e-05	0.00287991	synonymous-codon, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712786	GTACTTATACAGGAT[A/G]GTCTGGGGGAGCACC	54476
rs139340383	snp	C/T	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682145	TGCTAGGAAAAACCG[C/T]TGGCTTTCTTTCCCC	54476
rs139348090	snp	A/G	0.117537	0.212022	intron-variant	RNF216	GRCh38.p7	7:5646668	ACTGCACTCCAGCCT[A/G]GCGACAGAGCGAGAC	54476
rs139360275	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679665	CTGAAATCGAGAGAA[C/T]AGCCCTGTCATGGAA	54476
rs139367100	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5759271	GTGAACCAATTAAAC[C/T]TCTTTTCTTTCTTTA	54476
rs139374471	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5718659	ATGTTCAAGCAATTC[G/T]CGTGCCTCATCCTCC	54476
rs139382416	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5637889	CTTGTTCTGTTGTCC[C/T]GGGTGGAGTGCGGTG	54476
rs139388908	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670908	GAAGGCAGGACTCAA[A/G]GTCTTCCCAAGACGA	54476
rs139431776	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5631115	TTTCTCCCCTTACAA[C/G]ACGTAACAGGACAAA	54476
rs139448611	snp	A/C	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5765624	GAGAGCGAGACCCTG[A/C]CTCTGAAACAAACAA	54476
rs139489627	snp	C/G/T	0.00636936	0.0560724	intron-variant	RNF216	GRCh38.p7	7:5686202	CACTCCAGCCTGGGT[C/G/T]GACAGAGTATGACTC	54476
rs139499016	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5628433	ACAGGACACTGTGCT[C/T]AATAACTTTAATACA	54476
rs139524499	snp	C/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5686386	CCTGAAGGGGGCTGG[C/G]ACAGAAAACAGGATC	54476
rs139529495	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5629557	GGAGGGGCCAGAAGC[A/G]GCGTCTTGCGCCTGT	54476
rs139552996	snp	A/G	0.0236746	0.106192	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768827	CCACCACGCCCGGCT[A/G]TTTTTTTGTATTTTT	54476
rs139553204	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5683654	TAACCTGGAGCCTCA[A/G]TGTCCTCATCAAGGA	54476
rs139565357	snp	A/C	0.0482946	0.147699	intron-variant	RNF216	GRCh38.p7	7:5765760	CCAGCCTGGGCAACA[A/C]AGTGAAACCCCGTCT	54476
rs139567426	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5716087	ATTAGAAATGGGGTG[C/T]TGCTATGTTGACCAG	54476
rs139597896	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5650372	CAGTGCCAGGAACCG[A/G]TAGGACAATCAGAAT	54476
rs139624565	snp	A/G	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754660	AAGACCCCTGCACCC[A/G]CAGGAAATTGTAGAT	54476
rs139628351	snp	A/T	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5732611	TCATTTCTAGTTTAA[A/T]CCCTTCATTATGTTT	54476
rs139630621	snp	C/T	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5682567	TGCCCACCACCATGC[C/T]GGGCTATTTTTGTAT	54476
rs139636911	snp	A/G	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5649913	TGTTCGATAATCAGA[A/G]AACACCAGCAGCCAG	54476
rs139686645	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5740907	TTTTTTTTTGCAATG[-/A]AAAAAAAAAAAGAAA	54476
rs139706028	snp	A/G	0.00676609	0.0577691	intron-variant	RNF216	GRCh38.p7	7:5692606	GAGAAAGGCAGAGCT[A/G]CTCAGTTCCAGCTCC	54476
rs139723150	snp	A/G	0.00953873	0.0683987	intron-variant	RNF216	GRCh38.p7	7:5694326	CCGCCACTGCTACTC[A/G]ATGATATTCTCTTTA	54476
rs139725263	snp	C/T	0.00597247	0.0543191	intron-variant	RNF216	GRCh38.p7	7:5660699	CCTCCCACCTCAGCC[C/T]CCCAAGTAGCTGGGA	54476
rs139731246	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5646078	TTTTTCCCTGTGAAT[A/G]GGCCATACTTTCCTG	54476
rs139753577	snp	C/T	0.00676609	0.0577691	intron-variant	RNF216	GRCh38.p7	7:5743587	TACACAGAATGATTC[C/T]ATTTACTTAAAATAT	54476
rs139760750	snp	C/T	0.0146672	0.084371	intron-variant	RNF216	GRCh38.p7	7:5774945	GTAGAGATGAGGTTT[C/T]GCCATCTTAGGTTGG	54476
rs139763069	snp	A/G	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5775506	ATGCCTGCCACTTCT[A/G]CAACAGATTTGGGGG	54476
rs139765303	snp	C/T	0.0170251	0.090679	intron-variant	RNF216	GRCh38.p7	7:5723743	ACAGAGGAGGGAGAA[C/T]CGTGTCTCACTCTTT	54476
rs139784853	snp	A/G	0.144586	0.226689	intron-variant	RNF216	GRCh38.p7	7:5730823	ATTACAAAGTCTGCA[A/G]AAACAAATGATGTTA	54476
rs139787600	in-del	-/AAC	0.153	0.230415	intron-variant	RNF216	GRCh38.p7	7:5730643	TCTTCCCACAGAGAT[-/AAC]AACAACAACAACAAC	54476
rs139790780	in-del	-/AAAG			intron-variant	RNF216	GRCh38.p7	7:5747773	AAAAAAAAAAAAAAA[-/AAAG]GGGAAAAAAAAAGAA	54476
rs139799005	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5731191	ATGAACAAGTAAGAA[A/G]TGGAAAACTGTGTGT	54476
rs139851569	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5738857	GAAACAACTCAGTTA[G/T]CATAATTCTATAACC	54476
rs139859373	snp	C/T	1.65113e-05	0.00287322	synonymous-codon	RNF216	GRCh38.p7	7:5623052	GGGGAAGGGTGGGTG[C/T]GCGAAGGCATAGGGT	54476
rs139878741	snp	A/G	0.0142736	0.0832652	intron-variant, downstream-variant-500B	RNF216, RNF216-IT1	GRCh38.p7	7:5662362	CATAAACAGAGATAG[A/G]CTCCATGAAAGTGTT	54476
rs139879708	snp	C/T	7.07464e-05	0.00594712	synonymous-codon, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711833	CGGAAAGCTACAGGA[C/T]GGGCACCTAGAGTCA	54476
rs139908682	snp	C/T	0.00318978	0.0398085	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5621090	AGCCCGGCCTCCCTG[C/T]GCACCCTTACCCCAG	54476
rs139909418	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5698242	TCTTCTGGTTGCAGC[A/T]GGACTGCATGTAAGC	54476
rs139916912	snp	A/G	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5642349	CTCCCAAGTAGCTGG[A/G]ATTACAGGCGCCCAC	54476
rs139918029	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5689079	GCCGATTCTGTGAAA[C/T]AAAATGATATCCTAT	54476
rs139938845	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5710392	ACAAAAACAAAAAAC[A/G]TCCTCAGAGAATAAT	54476
rs139940414	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5697988	TCTTTGGGCTAGAAT[C/G]TGGATCAGCTTCTCA	54476
rs139958154	snp	A/G	0.0154538	0.0865337	upstream-variant-2KB	RNF216	GRCh38.p7	7:5781807	GCATCCGGGCTCTCC[A/G]CCTGCGGAGACTTGA	54476
rs139967827	snp	C/T	0.00874735	0.0655527	intron-variant	RNF216	GRCh38.p7	7:5772352	ACAGAAAAAATTCCA[C/T]GGACAACAGTTACAA	54476
rs139972246	snp	C/T	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5706787	CTTAGTAGTCACTTG[C/T]CTGTTTTTTGCTTTT	54476
rs139976080	snp	A/G	0.00557542	0.0525036	intron-variant	RNF216	GRCh38.p7	7:5695564	AGAGCAGAAGACACC[A/G]CAGCTATAGACAAGT	54476
rs139991671	snp	C/T	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5726408	CCTCTTTACTCTCCC[C/T]TAACCTGCTTCCCCC	54476
rs139999858	in-del	-/CT	0.039522	0.134904	intron-variant	RNF216	GRCh38.p7	7:5631838	TATATCCACACTTCA[-/CT]GTCAAGCCCACTCAG	54476
rs140026889	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5778373	AGAGAAAAATTGTTC[C/T]TGATTATCCCCTAGA	54476
rs140089677	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678285	TTTTACTGCCATCTA[C/T]AAGACTTTCAATTAT	54476
rs140133975	snp	C/G/T	6.6011e-05	0.00574466	synonymous-codon, missense, intron-variant	RNF216	GRCh38.p7	7:5741723	AAATGCTGCTCTAGA[C/G/T]TTTTTAGGCCTTTCT	54476
rs140143477	snp	A/C	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5723247	TAATTATCAATGCTA[A/C]AAATTAAAAAAATTT	54476
rs140149733	snp	A/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5632262	ATGACAGACCATGGT[A/G]CATCCCCTCGAGGGC	54476
rs140155895	snp	A/C	0.00279162	0.0372561	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662679	GCCAGAGAGAGGGAT[A/C]GGTATAAAACGAAGC	54476
rs140180290	snp	C/G	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5721483	TACTGAGGACATTTG[C/G]GTTTGCTGTTTTGGG	54476
rs140187314	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5747484	ATCAGACGTGACCCT[C/T]AGAAAGCCATTTCCA	54476
rs140188930	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5704983	AAAACGTTGCTGAGG[A/G]GCATAAAAAGATGTG	54476
rs140195158	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5647084	AACACAATCCACTGG[C/G]AGGCTGTTTCAGCCC	54476
rs140248700	snp	A/C	0.0142736	0.0832652	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673154	CACCAAATGCCCCAC[A/C]TGCGGGCAGTACCGC	54476
rs140252359	snp	A/G	6.58924e-05	0.0057395	missense	RNF216	GRCh38.p7	7:5729472	TTGAGCTCGTGCAGG[A/G]CCCACTTGATGTCCT	54476
rs140264038	snp	A/G	0.000329419	0.0128297	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741187	CCTTGCTGGGGTTCC[A/G]GCCTTGGAAAAGCGG	54476
rs140274722	snp	A/G	0.00597247	0.0543191	intron-variant	RNF216	GRCh38.p7	7:5659513	GGACCATGGTCACCC[A/G]GTAGGACTGAGGCTA	54476
rs140274759	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5625298	AGGGATGGTGGTCCC[A/T]GATATCGTGAGAGGA	54476
rs140276083	snp	A/T	0.0444908	0.142359	intron-variant	RNF216	GRCh38.p7	7:5755212	GAAGGGAGGGAAGGA[A/T]GAAAGGAAGGAAGGG	54476
rs140276182	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5725169	ACTTCCTAAAAATTT[C/T]GATGTGCTGAGAAAA	54476
rs140309187	snp	C/T	0.00107352	0.0231432	missense, upstream-variant-2KB	RNF216	GRCh38.p7	7:5752970	GGCCCATCTCGGAGA[C/T]TGATCCACTCTACAG	54476
rs140322792	in-del	-/T	0.0166325	0.0896639	intron-variant	RNF216	GRCh38.p7	7:5641559	TTTAATTGTATGACC[-/T]TCAGTAAATTACTCA	54476
rs140329267	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669025	TGATTTTTAGTTCTG[C/T]GGACCTAATATTATA	54476
rs140338435	snp	A/G/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5657205	ACTGACATGCCACAG[A/G/T]GCATTACGCTGTTGC	54476
rs140349028	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5653936	CCTGGAGGCCTGCAC[A/G]CACCAGACCAGGCAA	54476
rs140369462	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5643455	GGAGCTGTGACTGTG[C/G]TTGCTGACCTTGCGC	54476
rs140382034	snp	A/G	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5773768	AGAAGTGGTTTTGTC[A/G]TGTTGGCCAGGCTGA	54476
rs140385155	snp	C/T	0.046775	0.145601	intron-variant	RNF216	GRCh38.p7	7:5752030	TCTCTGCTAAAAATA[C/T]AAAAATTAGCCAGGC	54476
rs140387974	snp	A/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5699206	CTCCTTCAGTATAAT[A/T]TTGAAGCAAATCCCA	54476
rs140399578	in-del	-/GAA	0.269538	0.249235	intron-variant	RNF216	GRCh38.p7	7:5755153	GAGGAAGGAAAGAAG[-/GAA]GGAGAAAGGAAGGAA	54476
rs140402230	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5735877	AGGCAGATGGATCAC[C/T]TGAGGTCAGGAGTTC	54476
rs140419167	snp	C/T	0.0839998	0.186933	intron-variant	RNF216	GRCh38.p7	7:5640048	ACAGGCGTGAGCCAC[C/T]GCGCCCGGCCAATTT	54476
rs140462941	snp	A/C	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663069	TTCAAATACCAGTGG[A/C]TTGGGAAACCCAAAT	54476
rs140468073	snp	A/G	0.0107246	0.0724382	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782721	TGGGCATGGTGGTGC[A/G]TGCCTGTAATCCGAG	54476
rs140469844	in-del	-/AATAC	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5758307	TCACTACCAAGTTAG[-/AATAC]ATTATTAATAAAATC	54476
rs140481174	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5686686	GCTTTCAAAGGTAGC[A/G]CTATTTGCGGCAATG	54476
rs140585959	snp	C/T	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5779041	GAGCCACACCATTCC[C/T]AACTATGTTCTATTA	54476
rs140591253	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5770188	TTACTTGGGCTGGGC[A/G]CCGTGGCTCACATCT	54476
rs140602766	snp	A/C	0.000131994	0.00812277	synonymous-codon	RNF216	GRCh38.p7	7:5623034	AGGCCGCACGGGAGG[A/C]AGGGGGAAGGGTGGG	54476
rs140604013	snp	A/C	0.00914312	0.0669923	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712977	GCAAGGATCTCTCTG[A/C]CTGTTCATCTCTGAG	54476
rs140611837	snp	A/C	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5654942	GACTATTGCAGGAAG[A/C]TGGAGGACAAACAAC	54476
rs140612587	snp	C/T	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5717186	TGGAAAAACCCCATC[C/T]CTACTAAAAATACAA	54476
rs140631624	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767504	ACCAAGTTGTTAACC[A/T]ATGCCACATACATGC	54476
rs140657638	in-del	-/AT	0.0271762	0.113356	intron-variant	RNF216	GRCh38.p7	7:5777948	AGTAAGTACATCCTC[-/AT]GTGTGGAGGGTAAAA	54476
rs140661661	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5730891	CTTCAAATGCAATGG[C/T]TGAAGAATATAGTCC	54476
rs140715902	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5657803	GAACCCCTTAAATCT[A/C]AGGAGTTTATGCTGC	54476
rs140766113	snp	A/G	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5749457	CGTCGGGCCTATATG[A/G]ATGTTTTTTATATTC	54476
rs140800900	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5758633	TTAAGATTTAATGAC[C/T]GCCCTGCTGGGTTTT	54476
rs140808444	snp	A/G	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5770877	CAGTGGTGTGATCTC[A/G]GCTCACTGCAACCTC	54476
rs140809730	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5688002	TCCAGGAGGGAAAAA[-/C]CAGCCGTTTTGACAA	54476
rs140810152	snp	A/T	0.0103295	0.0711199	intron-variant	RNF216	GRCh38.p7	7:5719849	GCTTTGTGGCTCAGT[A/T]GCATAAGTGCTTTCC	54476
rs140819674	snp	C/G	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5751265	GAAACCCAAAATGAT[C/G]GTAACTGAGAGTGGC	54476
rs140826460	snp	A/T	0.00636936	0.0560724	intron-variant	RNF216	GRCh38.p7	7:5698637	AACCTCAAGCAATCC[A/T]CCTGCCTCATTCTCC	54476
rs140829811	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5643783	ACTATCTAGTTCCAA[C/G]AGACTTTTATAACCC	54476
rs140847393	snp	C/T	0.0704125	0.17392	intron-variant	RNF216	GRCh38.p7	7:5639673	CCATATTGGTCAGGC[C/T]GGTCTTGAACTCCTG	54476
rs140878341	snp	C/T	0.0189856	0.0955633	intron-variant	RNF216	GRCh38.p7	7:5727063	GGGGCTCATGTCCTG[C/T]GGCTACGCTGTTAGG	54476
rs140879521	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672031	TTTGCTAAGGCAGCC[A/G]AGCTGACCAAGACAG	54476
rs140884680	snp	G/T	0.00716266	0.059414	upstream-variant-2KB	RNF216	GRCh38.p7	7:5783323	TCAGTAGAGACAGGG[G/T]TTCACCATGTTGGCC	54476
rs140886736	snp	A/T	0.00874735	0.0655527	intron-variant	RNF216	GRCh38.p7	7:5729674	CATTTTAAGAATTAC[A/T]TGTGTAGAAAAGAAT	54476
rs140913066	snp	G/T	0.00119737	0.0244387	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5766897	GACTGATATTCACCA[G/T]ATAGCTGTATAATGA	54476
rs140921109	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5684094	CACAAGCTGGGCCTT[-/C]TTTTTTTTTTTTTTT	54476
rs140947767	snp	C/G	0.0356815	0.128715	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5780168	CATGGCATTTAGATA[C/G]TTTTTAGCATTCCTG	54476
rs140983256	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5641990	GTGAGCTGAGACCGT[A/G]TCACTGCACCCCAGC	54476
rs141012211	snp	C/T	0.000263848	0.0114828	missense	RNF216	GRCh38.p7	7:5715124	ACAAGTGAGCATCTG[C/T]GCACTGCGTCAGCTC	54476
rs141050143	snp	A/G	0.0037817	0.0433191	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741163	GGAGAAGAGGGGCCT[A/G]AAATCCCACCTTGCT	54476
rs141095885	snp	G/T	0.0158469	0.0875917	intron-variant	RNF216	GRCh38.p7	7:5651345	AATTCTCTTGCCTTA[G/T]CCTCCCAAGTAGCTG	54476
rs141103869	snp	C/T	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5685164	CATGGCCTCCAGTGA[C/T]TGGGCTGCCCATGTA	54476
rs141126915	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5704478	AGAAAGGTAAAAGCG[C/T]ATGCGCTAATAACAT	54476
rs141127587	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768472	GTACTATCAAAGAGC[C/T]TGACCTAACTGACAC	54476
rs141130903	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5646945	AAAGCCTAGGGTCTT[A/G]GGTTTTTCTGAGCAT	54476
rs141138684	snp	C/G/T	0.000148253	0.00860849	synonymous-codon, intron-variant	RNF216	GRCh38.p7	7:5741666	CCCAGAATCAAACAA[C/G/T]GGGTTGTTACACACT	54476
rs141182966	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5625526	GATGGGCAGCCCCAT[C/T]GAGGGCTAACCAACG	54476
rs141187642	snp	C/T	4.95413e-05	0.00497677	synonymous-codon, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712741	GTCGGCGTAGGCTGC[C/T]GCAACCTCCTCCTCG	54476
rs141191477	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5716584	ATCTGACTATAACTT[A/G]GCTGAACTGCAAACT	54476
rs141249582	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5657870	GCTCAGGTAGATTCA[A/G]TGAACTTTCTTTCCT	54476
rs141250652	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622496	AGGGAGATGCTCTCG[A/G]CTGCCTTGCTACCCA	54476
rs141291938	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5740743	ACCAGGCCACCATGA[C/T]ATGCAGTTAGAATCC	54476
rs141307445	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5747789	AAGGGGAAAAAAAAA[A/G]AAAAAATAAATAATA	54476
rs141307955	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5690288	GCCAAGATCGCGCCA[C/T]TGCACTCTAGCCTGG	54476
rs141327139	snp	C/T	0.000940229	0.0216617	missense	RNF216	GRCh38.p7	7:5622946	CGAAGTCATAGTTGA[C/T]CCGCACGTTGGGCAG	54476
rs141362333	snp	C/T	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5632875	CCATGACGAAGCACA[C/T]GAATGGCACCACAGT	54476
rs141436824	snp	A/G	0.030665	0.119967	intron-variant	RNF216	GRCh38.p7	7:5719385	TCTGTCAAAAAAGAA[A/G]AGAAAAAAGCAAAGA	54476
rs141445117	snp	A/C	0.021333	0.101051	intron-variant	RNF216	GRCh38.p7	7:5625860	TGGATGACACTATTA[A/C]ATTCTCCTACATTCT	54476
rs141455777	snp	A/G	0.00795532	0.062565	intron-variant	RNF216	GRCh38.p7	7:5706145	GAATCGCTTGCACCC[A/G]GAAGGTGGAGGTTGC	54476
rs141463665	snp	A/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5649501	ATGACAGAATAAGAC[A/T]CTGTCTCAAGGCGAG	54476
rs141471971	snp	A/G	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5658762	TCTGTATCTGTGTAT[A/G]TTTTGCCATGTTATG	54476
rs141488468	snp	A/G	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5731933	GATTCTGCAGCCCCC[A/G]CCGGGGACCCACGTC	54476
rs141497510	snp	C/T	0.0456336	0.143994	intron-variant	RNF216	GRCh38.p7	7:5742819	CAGGCTGGTCTTGAA[C/T]TCCTGACCTCAGATG	54476
rs141505912	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670223	ACAGGCGTGAGCTAC[C/T]GTGCCTGCCCTGGAA	54476
rs141532178	snp	A/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753126	CCCGTGCACTTAAGC[A/T]TTAAGAGCCATGTTT	54476
rs141557075	snp	A/G	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5636931	GGCATGGGAAGCAAC[A/G]GGAGGAGGCAGCAGA	54476
rs141568436	snp	C/T	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5701325	TCTTCTGTTCCCTGA[C/T]GGGATTTTCCACCTG	54476
rs141581160	in-del	-/TA	0.0185938	0.0946107	intron-variant	RNF216	GRCh38.p7	7:5748950	TGTCTATATATGCGT[-/TA]TGTGTGTGTGGTATT	54476
rs141612538	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5722914	CTGAGGCAGGAGAAT[C/G/T]GCTTGAGCTTGGGAA	54476
rs141624175	snp	A/G	0.00318978	0.0398085	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669616	AGACTGTGTTGGCCA[A/G]GTGCAGTGGTTCACG	54476
rs141635295	snp	C/T	0.000214152	0.0103455	synonymous-codon	RNF216	GRCh38.p7	7:5641220	TGGTGAGCGGGGATG[C/T]TGGCAGAAATGGTCA	54476
rs141638980	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665405	TTGTTTTCATACACA[C/T]CTCACCTACCATTTC	54476
rs141653945	in-del	-/CCTCTGC	0.0349115	0.127424	intron-variant	RNF216	GRCh38.p7	7:5648187	CTCGGCTCACCATAA[-/CCTCTGC]CCTCTGCCCCATAGG	54476
rs141658543	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5693046	GCTTTTTTCACTTAA[C/T]ATCTTGGAGACAGCT	54476
rs141666546	snp	A/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5635997	AGTTTCTCGTAGCCA[A/T]AACCCAAGACAAACA	54476
rs141695228	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5764523	TGTGGTGGCATGCAC[C/T]TGTAATCCCAGCTAT	54476
rs141709754	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5714180	GTTGGCCAGGCTAGT[C/T]TCGAACTCCTAATCT	54476
rs141722619	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5733227	ACTGGCTTGAAAAGA[G/T]GCAATACAATGACTG	54476
rs141761024	snp	C/G	0.0236746	0.106192	utr-variant-5-prime	RNF216	GRCh38.p7	7:5761125	AAACATGGTGACCAT[C/G]TGTTTCAAAAGAACT	54476
rs141775246	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682247	ACTCCAAAAATCCCT[A/G]TCTTGTTCTGAAATC	54476
rs141778607	snp	C/T	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5648602	GCATGGTGGCGGGCA[C/T]TCATAGTCCCAGCTA	54476
rs141782937	snp	G/T	0.0185938	0.0946107	intron-variant	RNF216	GRCh38.p7	7:5684171	GCAGTGGCGTGATCT[G/T]GGCTCACTGCAAGCT	54476
rs141793467	snp	C/T	0.11963	0.213316	intron-variant	RNF216	GRCh38.p7	7:5633393	CCAGTCTGATCAACA[C/T]GGTGAAACCCCGTCT	54476
rs141808393	snp	A/G	0.0205511	0.0992634	intron-variant	RNF216	GRCh38.p7	7:5714386	GCCTCAGCCTCCCCA[A/G]TAGCTGAGATTATAG	54476
rs141824688	snp	C/G	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5645853	CGTCAGCCTCCCAAA[C/G]TGCTGGGATTACAGG	54476
rs141829014	snp	C/T	0.0236746	0.106192	intron-variant	RNF216	GRCh38.p7	7:5710429	TCCTCTTCTTTGGCC[C/T]TCCCAATTGTACATA	54476
rs141844853	snp	C/G	0.00597247	0.0543191	intron-variant	RNF216	GRCh38.p7	7:5766603	CAGAATCCAACAATG[C/G]TGAAACTCTATTCTC	54476
rs141882227	in-del	-/A	0.0368353	0.130617	intron-variant	RNF216	GRCh38.p7	7:5727575	TACAAAAAATGAAAT[-/A]AAAAAGATCATCCAG	54476
rs141885548	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677742	AGAGTCCTGGGAGTG[C/T]TGCTCAGGAAATCCT	54476
rs141900082	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5630381	AAGCCAATCATCTCG[C/T]ACCTTTTTTTTTCCC	54476
rs141923393	snp	C/T	1.66275e-05	0.00288331	intron-variant	RNF216	GRCh38.p7	7:5721207	GCAAAAGCATGCAGA[C/T]AACTATGTGTTAGGA	54476
rs141928733	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5697909	ACAGAGCAGGGGAGA[C/G]AAGGGCAAAAGGACA	54476
rs141931244	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5641648	TGTTTTGAGAATTAC[A/G]GACAAAATATAAAGT	54476
rs141942747	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5772283	GAAATTCTGGGAAGA[C/T]AGTAGTAGTAACAGC	54476
rs141968108	snp	C/G	1.64743e-05	0.00287	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741128	GGTCTTCAAACTCTC[C/G]TAGAGGATGGGCAGG	54476
rs141999640	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622163	TCCAGTGTACCGCAG[A/C]GGCCTGGCCTGGGAA	54476
rs142031164	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5685544	GTGAACTACATCAAG[A/G]CAAATTCTATTACTT	54476
rs142035220	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5626027	GTGTTCTGAGCAAGG[C/G]ATGAAGAGAGGAGAG	54476
rs142040572	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5646983	GCCCTAGACATGTAC[A/G]TAGTCTTCTAGATCT	54476
rs142045238	snp	C/T	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681976	GTGCCACAGCAACCT[C/T]AGACAATGGGTCACA	54476
rs142051743	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5624617	GCCCCCAAGGCTGGC[C/T]TTGGCTCCTGGGCCA	54476
rs142072392	snp	C/T	0.00993419	0.0697739	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680558	AGGCGCGCACCACCA[C/T]GCTCAGCTAATTTTT	54476
rs142079169	snp	C/T	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5650951	ACTCCTTCCATATCC[C/T]TCATATTTAAACTGG	54476
rs142095512	snp	C/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5776714	GTTTATCCTTTAAAA[C/G]CACAGCAGCCCCTGA	54476
rs142101643	snp	A/C	8.29497e-05	0.00643956	intron-variant	RNF216	GRCh38.p7	7:5725444	CAGACAAGGCCTAAA[A/C]ATTGAGAAAAGGAAA	54476
rs142117209	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5631984	GGACCCTGAGGCTCA[A/G]AAGATGCAGAGAGTG	54476
rs142133341	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5748738	AGTTATTAAGTAGTA[C/G]TAAGTAGTTAAGGCT	54476
rs142138967	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5688983	GGTAAAGGAAATACT[A/C]CTTTTTCTTCAAGTG	54476
rs142141787	snp	A/C/G	0.0103333	0.0711729	intron-variant	RNF216	GRCh38.p7	7:5698913	ACTGAACAAGCCACA[A/C/G]AACAGGACATTCGAA	54476
rs142146959	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5642871	AAACCTTCTCTGTAA[C/G]AGCACCCTGAGGCTG	54476
rs142160648	snp	C/G	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5774805	CTCTTGTTGCCCAGG[C/G]TGGAGTGCAATGGTG	54476
rs142162382	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5773212	ATCAAATTTGAACTG[C/T]ATCTAATCAAGTCCT	54476
rs142165156	snp	A/G	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5723373	AATGCAATTGGCCGG[A/G]TGCGGTGGCTCAAGC	54476
rs142171388	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782948	CTTATACCTGGAATC[C/T]GAACATTTTGGGAAA	54476
rs142198628	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5695806	TGCTTTGCCTGTAAA[C/T]GGATGTGTTTATTTA	54476
rs142213627	snp	C/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5653048	TAATCTCTGCAAAAT[C/T]CCTGTGCCCACAAGC	54476
rs142247709	snp	C/T	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5745682	AGGTGGGTGGATAAC[C/T]TGAGGTCAAGAGTTA	54476
rs142258556	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5730971	CCAGAAAAACTAAAC[A/C]AATAAACAAACAACT	54476
rs142260582	in-del	-/TCTC	0.338069	0.233974	intron-variant	RNF216	GRCh38.p7	7:5714762	AATAGGCTGCAAGGT[-/TCTC]TCTTTCTGAGGTAAC	54476
rs142265338	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5693336	AAAGTCTGCTGACCC[C/T]TGGTATGGATGTTTA	54476
rs142270559	snp	A/T	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5747797	AAAAAAAGAAAAAAT[A/T]AATAATAACTAGATA	54476
rs142276166	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5778240	TAGTAACAATGGTTC[A/G]GTTCCATGACTTGCT	54476
rs142309852	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5776076	CTGTACTAATACAAT[C/T]AATATTAAATCAATA	54476
rs142393636	snp	C/T	1.72644e-05	0.00293801	missense, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711817	CACTGTCCAACAGAG[C/T]CGGAAAGCTACAGGA	54476
rs142439690	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5697040	AAATCCACCCTCCTT[C/G]TTTTGTTCTGCATTG	54476
rs142450156	snp	C/T	0.0263992	0.111815	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663396	CCATCCTGGCTAACA[C/T]GGTGAAACCCCCGTC	54476
rs142451243	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5641075	GTCAAATTTTGTTAC[A/G]TATATTCAAAATATT	54476
rs142465556	snp	C/G	0.0142736	0.0832652	intron-variant	RNF216	GRCh38.p7	7:5637687	AACACAGGTGTGCAC[C/G]CACCACCACCCCTGG	54476
rs142502725	snp	C/G	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5763044	GGGGCCAAAGCAGCA[C/G]AACTACTGAACTCTG	54476
rs142503768	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5694157	AAAAGAAGAATCCAG[A/G]AAGGTCTTACTAAAA	54476
rs142506609	snp	A/G	0.00494779	0.0494916	intron-variant, nc-transcript-variant	RNF216, MIR6874	GRCh38.p7	7:5711906	TGGTTCCAGCTCCAT[A/G]TGGCTGTTCATATGA	54476
rs142510689	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677084	AGACCACATACATCT[C/T]CCTTGTTTTTAGGGC	54476
rs142515977	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5706334	ACAGCTGATCTCTAA[A/G]CAACTTAATCTGGCA	54476
rs142522400	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5707671	CAGTGATATCCTTGC[C/G]TTGTTCCTGATCTTA	54476
rs142586410	snp	G/T	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5718359	GCACTCCAGCCTGGG[G/T]GACAAAGCGAGACTC	54476
rs142588801	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5659859	AGCACACCTGTACTT[C/T]TTTTGTTAAGAAGAA	54476
rs142595961	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671996	AAACTGACAGCATAT[A/G]TAAGCCCCTAGTCTG	54476
rs142618248	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5758882	AGACGCAATTGTATT[C/T]AGCAATGTGAGAAGG	54476
rs142622230	snp	C/G	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5708672	TTTTTTCAGGAGCTT[C/G]CAAGCTCTTGCTTCT	54476
rs142625995	snp	C/G	0.00716266	0.059414	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754408	CTCAAGTGCTCCTCC[C/G]ACCTCGGCCTCCCAA	54476
rs142626701	snp	A/C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5704267	CGCCTCATTTCAGAG[A/C/T]GACAAGTTCCTGAAA	54476
rs142641769	snp	A/G/T	0.000148357	0.00861166	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5729558	GCGCTGGTCAAGAGG[A/G/T]GTCAATTTAGAATAG	54476
rs142673786	snp	G/T	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5717739	GCCAGGATGCATGGT[G/T]AAATGAAAAATGCAG	54476
rs142679137	snp	A/G	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5625174	GGCAAACCCAAACAC[A/G]CCAACTGCCGGCTCA	54476
rs142681659	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5659534	ACTGAGGCTATAGGA[A/G]GGAGTTTGGAAAGCT	54476
rs142745235	snp	A/G	0.0551013	0.156571	intron-variant	RNF216	GRCh38.p7	7:5723518	CGGACTCGGTGGCGG[A/G]CACCTGTAGTCCCAG	54476
rs142786254	in-del	-/TCCCTG	0.32627	0.238082	intron-variant	RNF216	GRCh38.p7	7:5736118	AAATAGCTCTCCCTC[-/TCCCTG]TCCCTGTCCCTGTCC	54476
rs142811519	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5750814	GCAGTGAAAATTTCA[C/G]CATCAGTAGTAGCCT	54476
rs142840210	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5714088	GCTCACTAAGCCTCC[C/T]GAGTAGCTGGATTAC	54476
rs142842205	snp	C/G	0.00438332	0.0466095	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620896	GTCTACAGCCGCCCT[C/G]TGCTCCCAGAGATCC	54476
rs142856516	snp	C/T	0.00199481	0.0315187	intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652026	TTATTATCACAGGCG[C/T]ATCATTTTGTATTCT	54476
rs142884002	snp	C/G	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5630872	GAAACCCTGGCACAG[C/G]GAGGTTGTGACCCAG	54476
rs142896615	snp	C/T	0.0142736	0.0832652	intron-variant	RNF216	GRCh38.p7	7:5661767	GAGATTGTGCCACTA[C/T]ACTCCAGCCTGGGCG	54476
rs142900953	snp	C/G	0.0111196	0.0737302	intron-variant	RNF216	GRCh38.p7	7:5627870	CTGTGGCACTGCTGA[C/G]GCTGAGAGCATGCAG	54476
rs142903608	snp	C/T	0.0558544	0.157504	intron-variant	RNF216	GRCh38.p7	7:5710277	AGGCAGGAGAACTGC[C/T]TGAAGCCAGGAGGCG	54476
rs142939679	snp	C/G	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5720136	TGCTTTTGTTCTGCT[C/G]GTACAAACTCAATAT	54476
rs142956703	snp	C/T	0.00173701	0.0294192	synonymous-codon	RNF216	GRCh38.p7	7:5623094	CTGTGGCAGGTTCTG[C/T]GGAACGGGCCTCGGG	54476
rs142959409	snp	C/T	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5766693	TGCTATTTTGTTAGT[C/T]TATGGTATCAGTCAG	54476
rs142965082	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674722	ATTTATAGTTGTGCA[A/G]AGCGGGGGGTCTTTA	54476
rs142975956	snp	C/G	0.031825	0.122064	intron-variant	RNF216	GRCh38.p7	7:5635144	CTGCAAAATAGGAAA[C/G]CACTGCCTCCCAGTC	54476
rs142981591	snp	C/T	0.00953873	0.0683987	intron-variant	RNF216	GRCh38.p7	7:5747221	GATAAAAACAGGTCA[C/T]AGTTTAAAAATGTCC	54476
rs142994950	snp	C/T	0.00953873	0.0683987	intron-variant	RNF216	GRCh38.p7	7:5716468	TTTCCTTTATGAGTG[C/T]ATCTGATGAATGTCA	54476
rs143023635	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5629851	AAAAAAAAAAAAAAG[-/A]GGGAGGGAGGGTTTA	54476
rs143024330	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5756856	GCCCAGGCTGGCCTC[A/G]AAATCCTAGGCTCAA	54476
rs143035647	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5694355	TAAGGAATGACTTCT[C/G]AGTTAACTTTTGATT	54476
rs143068141	in-del	-/AAGG	0.171704	0.237423	intron-variant	RNF216	GRCh38.p7	7:5755240	GGGAGGGAAGGATGA[-/AAGG]AAGGAAGGAAGGAAG	54476
rs143093987	in-del	-/AC	0.0372196	0.131242	intron-variant	RNF216	GRCh38.p7	7:5704948	CATCATGTAATCATA[-/AC]ACACATTCTCTCCAC	54476
rs143098530	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5777609	AGACGCTGAGATCAG[A/G]TGACCACAGGATGGT	54476
rs143100355	snp	A/G	0.0103295	0.0711199	intron-variant	RNF216	GRCh38.p7	7:5641590	CCTGCCTGGAGACTC[A/G]GTTTCCTCATTTTTA	54476
rs143117476	in-del	-/GCTCA	0.00119737	0.0244387	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621847	CAGGGCTGAGCTGAT[-/GCTCA]GCTGACTCCATGAGA	54476
rs143118654	snp	A/C	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5704541	CGATTTGCTTTGGTA[A/C]TGAGCCCAAAAGAAC	54476
rs143167536	snp	A/C	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767824	GGGTGGTCTCGAATT[A/C]CTGACCTCAGGTGAT	54476
rs143203704	snp	C/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5693352	TGGTATGGATGTTTA[C/T]AGAAAAAGTCTGCTG	54476
rs143238225	in-del	-/GT	0.0524604	0.153226	intron-variant	RNF216	GRCh38.p7	7:5707704	AAAAAAAGCTTTTCA[-/GT]GTGTGTGTGTGTGGT	54476
rs143246697	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681727	ACCAGACCACACTGC[A/G]AAACCACACTGCTCA	54476
rs143250609	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5658396	GCACAGTGGCTCATG[C/T]CTGTAGTCTCAGCAC	54476
rs143257527	in-del	-/AAAACAAAAC			intron-variant	RNF216	GRCh38.p7	7:5705918	ATCTCAACAAAAACT[-/AAAACAAAAC]AAAACAAAACAAAAC	54476
rs143270208	snp	C/G	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5764336	GGTAGAACTACCAGA[C/G]GTAAAACAAAGATAA	54476
rs143306235	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5690070	TGGGTGGCTCATGCC[G/T]GTAATCCCAGCACTC	54476
rs143318542	snp	C/T	0.00067537	0.0183638	missense	RNF216	GRCh38.p7	7:5761005	ACAAACAACTTACCT[C/T]GTCCCCGATGGCAGT	54476
rs143322831	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677413	CTTTTGGTTTTCTTG[C/T]CATTTTCTCAGGCTT	54476
rs143322896	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5642109	GATAAAGTGCATTTA[C/G]TACTATTACCTTAAT	54476
rs143340839	snp	C/T	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5701191	TGGACTAAAGGAGAG[C/T]TGTCATTTCTTATAG	54476
rs143348337	snp	C/G	0.0197687	0.0974348	intron-variant	RNF216	GRCh38.p7	7:5729951	GAAGATCAAGCAACA[C/G]ATCTTAATAAAGTTA	54476
rs143368414	snp	A/G	0.00676609	0.0577691	intron-variant	RNF216	GRCh38.p7	7:5738208	TTATTTTTTAAAAAA[A/G]CATATTTACCACTTA	54476
rs143382271	snp	A/G	0.0607341	0.163335	intron-variant	RNF216	GRCh38.p7	7:5654508	CCTGGCTAACATGGC[A/G]AAACCCCACCTCTAA	54476
rs143386646	snp	C/G	0.0134861	0.0810011	intron-variant	RNF216	GRCh38.p7	7:5688114	ATTCCTGCTCTATGT[C/G]CTGGATTCCCACAGT	54476
rs143443798	snp	C/T	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5696484	AATGCAGCAAAGCAG[C/T]AACTGCCCAATGATC	54476
rs143447242	snp	A/C	0.0704125	0.17392	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5780101	TTTGGCTCCTAACCT[A/C]TAAAACAATGCCAAC	54476
rs143457943	snp	A/G	0.0170251	0.090679	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675664	AACAAACAAACAAAC[A/G]AACAAAGGAGCAAGG	54476
rs143510367	snp	C/T	0.00795532	0.062565	intron-variant	RNF216	GRCh38.p7	7:5757912	GTAATCCTAGCACTT[C/T]GTGAGGCAGAGGCAA	54476
rs143520636	in-del	-/AAAG	0.499653	0.0131743	intron-variant	RNF216	GRCh38.p7	7:5776949	GAGAGAGAGAGAAAA[-/AAAG]AAAGAAAGAAAGAAA	54476
rs143526971	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5706802	CCTGTTTTTTGCTTT[C/T]GTCACCTTGTTTTTG	54476
rs143539237	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5719433	GTTGAGTCCAGGTCT[A/G]AGAAAGCAGAAGCTG	54476
rs143545110	snp	C/T	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5745578	TACAGATAATAATGG[C/T]AAGGTGATTGAGTAT	54476
rs143549897	in-del	-/CT	0.0329836	0.124112	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621928	TGCCTTCAGCAACCA[-/CT]GAGAACACCCGGGGC	54476
rs143559244	in-del	-/T	0.0414363	0.137845	intron-variant	RNF216	GRCh38.p7	7:5742514	TAAAACAAGACAGTA[-/T]TTTTTTTCCCTGTAA	54476
rs143621805	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664441	TGCTTGCAGATGGTG[C/T]GAGAAAGTACTGCAT	54476
rs143659486	snp	C/G	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5759915	GGATTACAGGAGTGA[C/G]CCACCACGCCTGGCC	54476
rs143659761	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5709408	CTGGTTTCTGGATTT[C/T]TCACAGAGAGAAATG	54476
rs143677963	snp	C/G	0.000248256	0.0111385	missense	RNF216	GRCh38.p7	7:5622913	GCAGGTTGTGCTCCA[C/G]GGGCATGTGGATGGG	54476
rs143692826	snp	A/C	0.000313405	0.0125142	synonymous-codon	RNF216	GRCh38.p7	7:5725349	CTTGAAATCAATGTA[A/C]GAATACTGGTTCATT	54476
rs143696879	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5630016	CACCATCCTGTGAAG[A/G]GGACACTTGGAAAAA	54476
rs143720165	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5659296	TCTTCATGACATTTA[C/G/T]GTTTTACTGAAAAAC	54476
rs143724644	snp	C/T	0.00676609	0.0577691	intron-variant	RNF216	GRCh38.p7	7:5719506	AGAGACTACAGGGGT[C/T]GGGTTAAGAGAGACT	54476
rs143732539	snp	A/G	0.00597247	0.0543191	intron-variant	RNF216	GRCh38.p7	7:5656762	CTTTATTCATTTTCT[A/G]CTGCCTGAATAATGA	54476
rs143742699	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5719054	TGAATAATGTTATTA[A/T]TATTATTAAGAACCA	54476
rs143756439	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5691768	CTAGTGTATGAAATT[A/G]AGGTCAGAGGAAACT	54476
rs143763679	in-del	-/ATT	0.419776	0.18351	intron-variant	RNF216	GRCh38.p7	7:5778747	GTTTCTTTTTTTAAA[-/ATT]ATTATTATTTTTGAG	54476
rs143765040	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5755854	GCTCCATTTTGGCAG[A/G]TAACACTAAACAAAT	54476
rs143768394	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5634766	TCACCCAGGGGCCTG[A/G]TGGGATCTGCTGAAG	54476
rs143769685	snp	A/G	0.0279526	0.114869	intron-variant	RNF216	GRCh38.p7	7:5742141	AACCTCTGCCTCCCG[A/G]GCTCAAGCAACTCTT	54476
rs143776752	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5684780	GGAAAAACAAAACTT[C/T]ACCTTTACAGAGTTC	54476
rs143792138	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5702728	TCACTATGCTTTTAA[A/G]TTTTAAAAAGTGAAA	54476
rs143807923	snp	C/T	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5625726	GATTAAACTTCAGAT[C/T]AACAATGAAACAGAA	54476
rs143820938	snp	C/G	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5689164	GGAGGGAGGTGGAAG[C/G]GGGTCCTGGAGTGCA	54476
rs143882264	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5631732	CAATCTTGGGAAACA[C/T]TGAACAAAACAACAC	54476
rs143882805	snp	A/G	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5632311	TCCTTGGTTTCTGGC[A/G]CAGGCCTTAAGAAGG	54476
rs143927745	snp	C/T	0.0154538	0.0865337	upstream-variant-2KB	RNF216	GRCh38.p7	7:5781808	CATCCGGGCTCTCCG[C/T]CTGCGGAGACTTGAC	54476
rs143928639	snp	C/T	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5772650	AATAGTCAAATAATA[C/T]CAGCATTTTCTCAAC	54476
rs143934639	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5721513	GTTAATCTGAATAGC[A/G]CTGCTTATAGCCATT	54476
rs143937607	snp	A/C	0.000511201	0.0159793	intron-variant	RNF216	GRCh38.p7	7:5720995	GAGCAAACCAGAATC[A/C]CAGAAACACACCCCA	54476
rs143961648	snp	A/G	0.0402882	0.136092	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675911	ACGGGGTTTCTCTAT[A/G]TTGGTCAGGCTGGTC	54476
rs143993723	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5758432	TTAAATGCTCTGAAA[A/G]CCAAATACACAGTTG	54476
rs144029002	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619649	TGCCATGGCCTCTCA[A/G]CCCAGGCACTTCCTG	54476
rs144046564	snp	A/G	0.0368353	0.130617	intron-variant	RNF216	GRCh38.p7	7:5685994	TTGGGAGGCTGAGGC[A/G]GACGGATCATCTGAG	54476
rs144054256	in-del	-/GCCGGA	0.030665	0.119967	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670994	GGTTCCGGGGGAGCT[-/GCCGGA]GTGGCAGCCTGCTCT	54476
rs144060677	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5627326	CAGGACCGTGCTGGA[C/T]GCTGCAGACACAGTG	54476
rs144079975	snp	C/T	0.00636936	0.0560724	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674098	GCAATGGCGTTATCT[C/T]GGCTCACTGCAACCT	54476
rs144089481	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5757323	TCTTCTCAGTGCACT[A/G]AATCTTTTATCATTA	54476
rs144112683	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5717704	AGAGAAAAATCCCTA[C/T]GAATTGCTGCAGAGT	54476
rs144140933	snp	G/T	0.0126979	0.078662	intron-variant	RNF216	GRCh38.p7	7:5646767	AAGTCTCTGTTGTAT[G/T]AGCTTAGTGGTCAAT	54476
rs144141253	snp	C/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5756141	TGAGGTGTCCGATGG[C/T]TTTATATGCACTGGC	54476
rs144145669	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5705559	CAGACTTTGTTCTCA[C/G]TCATGCTGCACATCC	54476
rs144145739	snp	C/T	0.00557542	0.0525036	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671048	TGTTATAGCAACAAA[C/T]GATACTTTTTTCTTT	54476
rs144171985	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5625354	GTCTAATGAAAGCAC[A/G]TTTATTTTCCTAGAC	54476
rs144201287	snp	A/T	0.0146672	0.084371	intron-variant	RNF216	GRCh38.p7	7:5740298	CGCCCGGCTAATTTT[A/T]AATTTTTTTAGTAGA	54476
rs144201399	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5775217	TTCTTCAGTTATCAA[C/G]TATTGCCCATTACAG	54476
rs144208347	snp	A/G	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5772841	AGAGTGCAATGGCAC[A/G]ATCTCGGCTCACTGC	54476
rs144222644	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5714618	AAAATACCACAAACT[C/T]GGTGGTGTAAAACAA	54476
rs144223400	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5777807	TGTGTATTTTTACAA[C/T]AGGAAAGGTTTTAAA	54476
rs144289497	snp	C/T	0.0103295	0.0711199	intron-variant	RNF216	GRCh38.p7	7:5657315	GCTCACACCTGTAAT[C/T]CCAGCACTTTGGGAG	54476
rs144289831	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622248	CAGAACAAAACCCCC[A/G]CCGCGAGATGGGTCT	54476
rs144342211	snp	A/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5711187	TTTTAAGACATTCTT[A/T]GTTCACAGGGCGCCA	54476
rs144342243	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5738810	AAAATGTCTTAACAT[A/C]TTGACTAAAACACAG	54476
rs144343442	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5774191	TTTAAATCTTGGTTT[A/C]CCATTTAGTCAATCG	54476
rs144350155	in-del	-/A	0.0325976	0.123435	intron-variant	RNF216	GRCh38.p7	7:5749483	ATTCCAAGATTAGAT[-/A]AAAGTTCCTAGAAAT	54476
rs144354510	snp	A/C/G	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5654031	GTGCCAAGTACGGAA[A/C/G]TAACACGATCAGGTA	54476
rs144366817	snp	G/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5730890	GCTTCAAATGCAATG[G/T]TTGAAGAATATAGTC	54476
rs144368964	snp	A/G	0.00358779	0.0422022	intron-variant, nc-transcript-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662523	AAACTGCTCTGGGTC[A/G]GTTTTGTTCAGAGCA	54476
rs144374257	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5694573	AGGTAAGTTTAAACG[A/G]CAAAACAAATCTCAG	54476
rs144406708	snp	A/G	0.0142736	0.0832652	intron-variant	RNF216	GRCh38.p7	7:5638291	TATATAAAATTTGAC[A/G]TATCTCCTGTTTTTT	54476
rs144408072	snp	A/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5751787	AAGGAAGTGTTCCTT[A/G]GTCCTAGAACCACAA	54476
rs144419531	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5748860	CACCATGTTGTTCAA[C/G]TGTAAACTGTATTTG	54476
rs144447272	snp	G/T	0.00557542	0.0525036	intron-variant	RNF216	GRCh38.p7	7:5659631	TTAAAGGGATGGTTT[G/T]CTGGGGTTGTAGGAC	54476
rs144480512	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5691386	GGATTGCTCCTGGCT[A/G]GATTGCTCCAGGCCC	54476
rs144521867	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5624679	GAGGATGGTCCCCCT[C/T]GGACCTTGCCGTCTC	54476
rs144538592	snp	C/T	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5703820	CCTAAACCTCCACCT[C/T]GTGGCCCTAAGTTTC	54476
rs144544407	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5747242	AAAAATGTCCTAAAC[C/G]TGGGGAAGACTTTCA	54476
rs144545142	snp	C/T	0.00795532	0.062565	intron-variant	RNF216	GRCh38.p7	7:5743661	GTACCCACATGTATA[C/T]ACACATGGATACATA	54476
rs144553722	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5714347	CACCACAACCTCTGC[C/G]TCCCAGATTCAACCA	54476
rs144554966	snp	G/T	0.00557542	0.0525036	intron-variant	RNF216	GRCh38.p7	7:5656441	AACATGAAGAACAGG[G/T]TATCGTGGCCATCGC	54476
rs144561576	snp	A/C	0.00795532	0.062565	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669360	ATCTTTGCCACTGGC[A/C]ATCACAGGGAGGCTG	54476
rs144580837	snp	C/G	1.91079e-05	0.00309088	missense, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711765	TGCCTCCCTACCTTT[C/G]GGCAGTGAGGATTAG	54476
rs144610324	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5752689	GACTGAAACATACAG[A/C]TTCTAAATCTAAGAG	54476
rs144611882	snp	A/G	0.0126979	0.078662	intron-variant	RNF216	GRCh38.p7	7:5700661	TACCCATAGAAACTC[A/G]TTAAAAATCCACAGA	54476
rs144615363	snp	C/G	1.65124e-05	0.00287331	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5729568	AGAGGGGTCAATTTA[C/G]AATAGTCAAAAAAGT	54476
rs144647624	snp	C/G	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5749494	TAGATAAAGTTCCTA[C/G]AAATCTGATATGTCT	54476
rs144654379	snp	A/C/G	3.29866e-05	0.00406108	missense	RNF216	GRCh38.p7	7:5715132	GCATCTGCGCACTGC[A/C/G]TCAGCTCCTCGAATG	54476
rs144665135	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750773	ATCTTTCCTTACTTA[C/T]GCCTCTCACGTGGCA	54476
rs144699233	snp	C/G	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5697427	CATGTCTCCATATAG[C/G]CAGATGACAGGCAGC	54476
rs144700087	snp	G/T	0.0217236	0.101931	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671632	ACATGGTGAAACACC[G/T]TCTCTACTAAAAATA	54476
rs144764233	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668491	GCCTCCCAAAGTGCT[A/G]GGATTACAGATGTGA	54476
rs144778068	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5746732	TCTTGCCTTTTCATG[C/T]ATAAAACTTCTGGCT	54476
rs144835147	snp	A/C/G	0.00128413	0.0253067	missense, synonymous-codon, intron-variant	RNF216	GRCh38.p7	7:5741672	ATCAAACAATGGGTT[A/C/G]TTACACACTGAAAAA	54476
rs144835691	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5763180	CAATGAGGGAGTGGG[C/T]AGATTAACTGTTAAG	54476
rs144853955	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666571	GAAGAAGAGCCTCTG[C/T]AATGGCTGTGCATGA	54476
rs144884604	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679932	CTTTAAGAAACACAA[C/T]AGGGACCCTGTATGC	54476
rs144890391	snp	G/T	0.02016	0.0983543	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622069	CGTCTCCCCCAGCAG[G/T]TGGGCTGCCCAGCAG	54476
rs144900235	snp	C/G/T	0.000708098	0.0188031	synonymous-codon, missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741177	TGAAATCCCACCTTG[C/G/T]TGGGGTTCCGGCCTT	54476
rs144917695	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5711080	GTTCAACTCTAATCA[C/T]GCAATTTTAGAAAAA	54476
rs144921627	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672276	GGCTTCCTGGAAGCA[C/G]CTGCCCCTAAATACA	54476
rs144947729	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5625882	CTACATTCTCTAGGC[C/T]TCAGATGCCAAGTGA	54476
rs144954302	snp	A/G	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5755526	TTTCTGCTCTCCTTC[A/G]TCCTCAAAGGGAGGA	54476
rs144988882	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5653685	AAATTATAACCCTAA[C/T]AGGTTACAGTGAAGG	54476
rs145004124	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5717107	GCCTGTAATCCCAGC[A/G]CTTTGGAAGGCCGAG	54476
rs145049113	snp	C/T	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5724617	CTAAGGGATTTTCTT[C/T]TAGAGCCTGAAAAGT	54476
rs145053953	snp	C/G	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5735674	GAGATTGTGGGAGAA[C/G]AGTTACAGAAGACAG	54476
rs145060051	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669148	TGGGCAGGACTGTCT[A/G]CACCTGCCAGCCTGA	54476
rs145070924	snp	C/T	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5714103	CGAGTAGCTGGATTA[C/T]AGGCACCCACCACCA	54476
rs145070983	snp	C/T	0.000364256	0.0134906	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741027	CTCTGCAGCTTCTTG[C/T]CCCCAAATGTTTTCC	54476
rs145074036	snp	C/T	0.00557542	0.0525036	intron-variant	RNF216	GRCh38.p7	7:5655587	CTCCAGCCTGGGCAA[C/T]AGAGCAAGACTCCAT	54476
rs145099684	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753107	AACGTACCTCCTCAA[C/G]CAGCCCGTGCACTTA	54476
rs145111269	snp	A/G	0.0142736	0.0832652	intron-variant	RNF216	GRCh38.p7	7:5650865	TGTAAGAGAATAATG[A/G]TACCCACCTGTGCTG	54476
rs145111310	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5686292	ACACCACTGCTGCCA[C/T]GTGGTTTCTGTGGGG	54476
rs145118313	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5752499	TTGTAAAATCCATAT[A/G]AAAATTTAAGTGCAA	54476
rs145184975	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5686573	GCACGCCAGTGTTCC[C/T]AAACTGATGTTCTAA	54476
rs145187193	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5629861	AAAAGAGGGAGGGAG[A/G]GTTTAGGATTGATTT	54476
rs145198762	snp	C/T	0.118933	0.212888	intron-variant	RNF216	GRCh38.p7	7:5632594	CCAGCCTGGCCAACA[C/T]GGCGAAACCCCATCT	54476
rs145218883	snp	C/T	0.00795532	0.062565	intron-variant	RNF216	GRCh38.p7	7:5690016	TTCACCTGTATTATA[C/T]TTTACTTACATCTTT	54476
rs145223293	snp	A/G	0.040671	0.13668	intron-variant	RNF216	GRCh38.p7	7:5772847	CAATGGCACGATCTC[A/G]GCTCACTGCAACCCT	54476
rs145224504	snp	A/C	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5722249	TTTCTAGAAAACTTT[A/C]TCTCATTCAGATTTT	54476
rs145235855	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5775923	CAGGCTGGAAGAAGA[C/T]GACATGCCCGTGTCA	54476
rs145253223	snp	C/T	0.0103295	0.0711199	intron-variant	RNF216	GRCh38.p7	7:5727610	GGTGGCGTGCACCTG[C/T]AGTCCTAGCTACATG	54476
rs145264897	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673173	GGGCAGTACCGCACT[A/G]GTCACCAGCACCACC	54476
rs145269169	snp	C/T	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5642415	AATGGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT	54476
rs145281287	snp	C/G/T	1.6473e-05	0.00286988	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741567	TTCTCTTTCTGTTTG[C/G/T]CCACTTGGCTTAGTG	54476
rs145285373	in-del	-/G	0.00557542	0.0525036	intron-variant	RNF216	GRCh38.p7	7:5623623	TAAAGAAAAACAGAT[-/G]GGGTCTTGCTATTTT	54476
rs145337462	snp	C/T	0.0205511	0.0992634	intron-variant	RNF216	GRCh38.p7	7:5654103	GGAGGAAAGAGTGAA[C/T]GTGCAAAAGACAGAA	54476
rs145353709	snp	C/T	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5686511	AGTGCTGCTTAACCA[C/T]CAGTGCCTTTAGGAA	54476
rs145371895	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5758780	GACTTTACAGGCTCA[C/T]AGGTGGAAGGGACTA	54476
rs145380633	snp	C/T	0.00636936	0.0560724	intron-variant	RNF216	GRCh38.p7	7:5769448	AACAAAGAGGCTGGG[C/T]GTGGTGGCTCATGCC	54476
rs145381160	snp	C/T	0.00557542	0.0525036	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669711	CCAGCCTGGCCAACA[C/T]GGCAAAACCCCATCT	54476
rs145435141	snp	A/C	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767559	CAGCAGAGAAGCTAA[A/C]GAGCTGAGCAGAAAT	54476
rs145457116	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5650415	TTGTAAGTAATTCTC[C/T]TTCCAAGAAACATCT	54476
rs145494388	snp	C/G	0.000153988	0.00877328	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741605	AGATTCCAGGAGGCC[C/G]AAGATCCAGAAATTC	54476
rs145499795	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5639441	AAAGTGCCGGGATTA[C/G]ACCCATGAGCCACCA	54476
rs145520358	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5629855	AAAAAAAAAAGAGGG[A/G]GGGAGGGTTTAGGAT	54476
rs145556401	in-del	-/C	0.0193772	0.0965046	intron-variant	RNF216	GRCh38.p7	7:5649525	AGGCGAGAAAAAAAA[-/C]GTTTTGACATCTGGC	54476
rs145562709	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5733932	TGTAAAAATGTAGTC[A/G]TTGCTGCTCAATTTT	54476
rs145603102	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5736123	GCTCTCCCTCTCCCT[C/G]TCCCTGTCCCTGTCC	54476
rs145607960	snp	C/T	0.0146672	0.084371	intron-variant	RNF216	GRCh38.p7	7:5643603	GATGGTGGCATAAGC[C/T]ATGCCCTTCAGATCT	54476
rs145631108	in-del	-/T	0.118235	0.212457	intron-variant	RNF216	GRCh38.p7	7:5760092	TACACCTCAGCATGA[-/T]TTTTTTCCTTTTAGC	54476
rs145640320	snp	A/G	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5779497	AAGCAAGCCGACTAA[A/G]TTGAGATGTTTCATA	54476
rs145643906	snp	A/G	0.0119091	0.0762411	intron-variant	RNF216	GRCh38.p7	7:5737011	CCCGGCCGCCACCCC[A/G]TCTGGGAGGTGTTCC	54476
rs145645919	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5686732	AAGATCTTAAAACAG[C/T]GGTCCCCAACATTTT	54476
rs145646487	snp	C/T	0.0119091	0.0762411	intron-variant	RNF216	GRCh38.p7	7:5727380	ATGCTTATTATTGAG[C/T]GGCCAAGTCTATAAG	54476
rs145675936	snp	C/G	0.0558544	0.157504	intron-variant	RNF216	GRCh38.p7	7:5734721	CCCAGCTATTCGGGA[C/G]ACTGAGGCAGGAGAA	54476
rs145676952	snp	C/T	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5770595	GTAGATTTAATACAA[C/T]CTTTATCAGGTTTTA	54476
rs145721455	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5685577	TCCTCTTTCCTCAGC[A/G]AACTGAAAAGACAAA	54476
rs145744740	snp	G/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5692770	AATCACATTTCTATT[G/T]TTCAAGTTCTCTTAA	54476
rs145774169	snp	A/G	0.00993419	0.0697739	intron-variant	RNF216	GRCh38.p7	7:5775660	GGATTATTTGAGGTC[A/G]GGAGTTCAAGACCAG	54476
rs145782649	snp	C/T	0.0539704	0.155153			GRCh38.p7	7:5780196	CTGGCAATTCCGTTA[C/T]TAATTCATGGGTCTT	54476
rs145800933	snp	G/T	1.65504e-05	0.00287662	missense	RNF216	GRCh38.p7	7:5623077	TAGGGTGGCATCTGT[G/T]GCTGTGGCAGGTTCT	54476
rs145813542	snp	C/T	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5774235	AATTGTTCAATCTCC[C/T]AGGCCAATTTCCTCA	54476
rs145839809	snp	C/T	0.0158469	0.0875917	intron-variant	RNF216	GRCh38.p7	7:5716187	ACGAGCCACGGTGCC[C/T]GGCCACCAACCCATT	54476
rs145845395	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5739113	CAGTTTGAGAAGATG[A/G]AAGAGTTCTGAAGAT	54476
rs145909845	snp	A/C	0.0189856	0.0955633	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663406	TAACACGGTGAAACC[A/C]CCGTCTCTACTAAAA	54476
rs145918553	snp	C/T	0.0217236	0.101931	intron-variant	RNF216	GRCh38.p7	7:5657841	GAGAATCAATAAAGT[C/T]CAGCAAAGTCAAAGC	54476
rs145934676	snp	A/C/T	0.000501309	0.0158245	synonymous-codon, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711818	ACTGTCCAACAGAGC[A/C/T]GGAAAGCTACAGGAC	54476
rs145943349	snp	A/G	0.0126979	0.078662	intron-variant	RNF216	GRCh38.p7	7:5722476	CTCACTGTCAGCTCC[A/G]CCCCCCGGGGTTCAC	54476
rs145945121	snp	A/C	0.00318978	0.0398085	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664941	AGCTGGGATTACAGG[A/C]GCCCGCCACCAGGCC	54476
rs145982348	snp	C/T	0.000153988	0.00877328	synonymous-codon	RNF216	GRCh38.p7	7:5623022	GTTGTTGAACACAGG[C/T]CGCACGGGAGGCAGG	54476
rs145997996	snp	A/C	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5710338	GCACTCCAGCCTGGG[A/C]AACAGAGTGAGACCC	54476
rs145999913	snp	C/T	0.00795532	0.062565	intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652110	CATAAGCAACACTAG[C/T]GCAGTCTAAGTTAAT	54476
rs146001683	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5706445	TCTATGAGTCTGACT[A/G]CTTTAGATCCTGCAT	54476
rs146003009	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5650170	AAGCTAGGCTCATGA[A/C/T]AGAAGCATCCTCTAT	54476
rs146020484	snp	C/T	0.0189856	0.0955633	intron-variant	RNF216	GRCh38.p7	7:5732595	TATAAACTGTCAAAA[C/T]TCATTTCTAGTTTAA	54476
rs146067142	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5623915	TGGCCGCGTGGGTGA[A/G]GTCAGGTCTATAGCC	54476
rs146096829	snp	C/T	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5745736	GAAACCCCATCTCTA[C/T]TAAAAACACAAAAAT	54476
rs146102863	snp	C/G	0.00279162	0.0372561	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620974	TGTTGCTGCCGCATG[C/G]AGCCTGCCTTTCCAA	54476
rs146117556	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5723218	ACATATTAAGTGCTC[A/G]ATGTTAATTACTGTA	54476
rs146121491	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665981	CGATCCTGGCTAACA[C/T]GGTGAAACCCCGTTT	54476
rs146124278	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5721366	CATCCATTTTTTGAC[C/T]TTTCTGATTCTTTCC	54476
rs146124434	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750427	CAAACTGGTCTTACT[C/G]TGATTATCTTTGGTA	54476
rs146124850	snp	C/T	0.0142736	0.0832652	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662634	CCACTGAGAGCCTTC[C/T]ATCAGTGCCGCTGAG	54476
rs146143379	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5747235	ATAGTTTAAAAATGT[C/T]CTAAACCTGGGGAAG	54476
rs146188395	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5637222	TCTGTCACACAGGGG[C/T]ACGGCCTGCCTTGTG	54476
rs146223611	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5634572	CAGGGAGGCAGGACA[A/G]TGTGCTGGGGAGGAG	54476
rs146242176	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682127	GGCCATGCGGGCCCA[C/T]GCTGCTAGGAAAAAC	54476
rs146256702	snp	A/G	0.111224	0.207945	intron-variant	RNF216	GRCh38.p7	7:5764573	GAATCGCTTGAACCC[A/G]GGAGGCGGAGGTTGC	54476
rs146307424	snp	A/G	0.0146672	0.084371	intron-variant	RNF216	GRCh38.p7	7:5651697	CTCTGTTGGCAGGCT[A/G]GAGTGCACTGGCGCA	54476
rs146343316	snp	C/T	0.0240643	0.107019	intron-variant	RNF216	GRCh38.p7	7:5756368	GCTTTCATGCTACAA[C/T]GGTATAGCTGAATAG	54476
rs146356109	snp	C/T	0.000247604	0.0111239	synonymous-codon	RNF216	GRCh38.p7	7:5623151	CACAGGCTTCTCCAG[C/T]GGGGGTCCAATGCGT	54476
rs146360745	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5694289	GTATGCAGTACTTGA[A/G]TCATTCACACTGAGC	54476
rs146364817	snp	A/T	0.0437281	0.141251	intron-variant	RNF216	GRCh38.p7	7:5725658	AGTTCGACACCAGTC[A/T]GGCCAACATGGTGAA	54476
rs146365219	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5692105	GACAGCAAGTAAGCC[A/C]GCAAATCATGCCTGG	54476
rs146369186	snp	C/T	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5634787	TCTGCTGAAGACATG[C/T]AGCAACAAGCACCAA	54476
rs146378724	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5777183	AGACATTGTGGAAGC[A/G]GATGCTCCAGCACTG	54476
rs146381773	snp	C/G	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5774885	GTCTCAGCCTCCCAA[C/G]TTACAGGCATGTTGC	54476
rs146383694	snp	C/T	0.0178098	0.0926698	intron-variant	RNF216	GRCh38.p7	7:5723503	ACACAAAAAATTAGC[C/T]GGACTCGGTGGCGGG	54476
rs146415631	snp	C/G	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5699837	AAGGCCATGTGGCCT[C/G]TGGGAACTGGAGATG	54476
rs146415638	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5731155	TTTTAAGAAAAGCAG[C/G]TACTCTTTGTCGAGA	54476
rs146419583	snp	G/T	0.0142736	0.0832652	intron-variant	RNF216	GRCh38.p7	7:5643743	GGGATATTTTGAGTA[G/T]TCACGATGTTATACA	54476
rs146434040	snp	A/G	0.0150606	0.0854603	upstream-variant-2KB	RNF216	GRCh38.p7	7:5783310	AATTTTCGTATTTTC[A/G]GTAGAGACAGGGTTT	54476
rs146453348	snp	A/C	0.0150606	0.0854603	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5780103	TGGCTCCTAACCTCT[A/C]AAACAATGCCAACCC	54476
rs146477262	snp	C/G/T	4.94176e-05	0.00497059	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741640	TAGTCATCCTCAGAA[C/G/T]CATCCTGTGCCCCAG	54476
rs146506071	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5704383	TGGCTCATGTCTTAA[A/G]TATCAGGAATCCTCA	54476
rs146541232	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5743783	TCAGGCTTTAGGGTG[G/T]GTCCCTGAGGACTAT	54476
rs146559368	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5740423	GAGCCAGCACGCCCA[C/G]CCCTTGTGTTACTCT	54476
rs146582389	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5770619	GGTTTTAAGAATAGA[C/T]ATATACTAGATGACT	54476
rs146605378	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5632128	GCTCACCCTGGACAG[C/T]GGTCTATAGAGGTTC	54476
rs146610184	snp	C/T	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5629599	TTTGGGAGGCCGAGG[C/T]GGGCGGATCACGACG	54476
rs146625838	snp	A/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5719185	CAGAAGTTCGAGACC[A/T]GCCTGGACAGCATGG	54476
rs146628573	snp	C/T	0.120674	0.21395	intron-variant	RNF216	GRCh38.p7	7:5660724	CTGGGACCACAGGTG[C/T]GCACCACCATGCCTG	54476
rs146641408	snp	C/G	0.0197687	0.0974348	intron-variant	RNF216	GRCh38.p7	7:5632680	TACTTGGGAGGCTGA[C/G]GCAGCAGAATCGCTT	54476
rs146660058	snp	C/T	0.00358779	0.0422022	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672472	ACACACATGATGTAG[C/T]GCTTGTAGCATCAAG	54476
rs146661715	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5706809	TTTGCTTTTGTCACC[C/T]TGTTTTTGGTATTAT	54476
rs146680178	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5704896	GTGAATGCTGTTATC[A/C]ATAGGTGAAAGTCAA	54476
rs146694552	snp	C/T	0.000602986	0.0173531	synonymous-codon	RNF216	GRCh38.p7	7:5622875	TCAGAAGCGATGCCG[C/T]GGCTGGGGGCCAAAG	54476
rs146724586	snp	A/G	0.117886	0.21224	intron-variant	RNF216	GRCh38.p7	7:5646643	GGTTGCAGTGAGCCA[A/G]GATTGCACCACTGCA	54476
rs146746929	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675679	GAACAAAGGAGCAAG[A/G]TCATGAAGCCTATAG	54476
rs146761775	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5758106	CAAAATATATCTCCA[A/G]AGTCAGTAATTTTCC	54476
rs146780227	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5721759	GCTGTATGATTTTCA[A/C]CCATTTTTATTTTCA	54476
rs146780514	snp	C/T	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5686682	ACAAGCTTTCAAAGG[C/T]AGCGCTATTTGCGGC	54476
rs146797537	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5769963	ACCCAGGAGGCCAAG[G/T]TGCAGTGAGCTGAGA	54476
rs146798958	snp	A/G	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5719456	AGAAGCTGAAACGGG[A/G]TCATTTGGCTGTGCC	54476
rs146799683	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677091	ATACATCTCCCTTGT[C/T]TTTAGGGCACTCTGA	54476
rs146814317	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767131	GCCTATAGTAGACCA[A/G]CCCTTTGCCTCTTCT	54476
rs146867877	snp	A/C	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5689224	GACGGGGGCAAAGGG[A/C]AGGCCTGGCTCCAGA	54476
rs146884509	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5772668	GCATTTTCTCAACTT[A/G]TAGAATGTGAAGTTA	54476
rs146886234	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5632530	GTAATGATGTGTCAG[G/T]CCAGGGTAGAAGTTA	54476
rs146897938	snp	C/T	0.00517822	0.0506191	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619873	AGCAGATCACCTGAT[C/T]TTCCTCCCTGGCAGG	54476
rs146911306	snp	A/C	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5709243	GAGCAGCCTCCTGAA[A/C]GGTCTGAATATTAGA	54476
rs146927618	snp	C/T	0.0146672	0.084371	intron-variant	RNF216	GRCh38.p7	7:5771800	GAAACCCTGTCCCCC[C/T]ACCAAAAAACATCTG	54476
rs146929135	snp	C/G/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5720179	AATATAGCTGAGCTT[C/G/T]ATCAACAGAGATGTG	54476
rs146971908	snp	A/G	0.0107246	0.0724382	intron-variant	RNF216	GRCh38.p7	7:5693119	TATGGTATATGCTAC[A/G]GGTTGGCAAACTACA	54476
rs146973775	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5636129	ACCTCAGCTACCACT[C/T]CTGTGGCCATGCAAG	54476
rs146988321	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5690382	CCTGTTTCTCTAAAA[C/G]CATGGTTAGCAATGC	54476
rs146988588	snp	A/G	0.0134861	0.0810011	intron-variant	RNF216	GRCh38.p7	7:5724593	CTTAGGAACCTCAGG[A/G]GTCACAGCCTAAGGG	54476
rs146989574	snp	A/C	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5632901	ACAGTGGGCAGTGCA[A/C]CCCAAATGCAGTGTC	54476
rs147077353	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5651036	AATCTAGACCAATGC[A/G]ATACGAGCGGAAGTG	54476
rs147087339	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5708204	AACAGAGGAGAAAAA[A/G]TGTTTTCTGTGCCTG	54476
rs147138829	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5657048	CACCTGGAAGGTGTC[C/T]GTCCCCATGCGTGCT	54476
rs147143189	snp	C/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5688156	GACACCAGGCTTTCA[C/T]GCACAGAACTGTGTA	54476
rs147151897	snp	C/T	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5738328	ATTCCTGGACTCAGG[C/T]AATCCTCTTGCCTCA	54476
rs147155325	snp	A/C	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5735721	TTCCAGAACTGACCA[A/C]CACCACCAATCTATG	54476
rs147171669	snp	C/G	0.0146672	0.084371	intron-variant	RNF216	GRCh38.p7	7:5769167	TCTGTTGCCAGACTG[C/G]AGTGCAGTGGCACAA	54476
rs147206013	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5774190	GTTTAAATCTTGGTT[C/T]CCCATTTAGTCAATC	54476
rs147242642	snp	A/G	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5705589	CCTCTTGGCAGAGGG[A/G]AAAAATGAACCATAT	54476
rs147243122	snp	A/G	0.00676609	0.0577691	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671484	GCTGATGGGGTGAGC[A/G]CTATTCCAATCTGAT	54476
rs147257676	snp	C/G	0.00914312	0.0669923	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753934	CGGGAGGCAGAGGTT[C/G]CAGTGAGCTGAGATC	54476
rs147260902	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5751232	ACACCAGAACCTATA[A/C]AGTATATGCTGGGAC	54476
rs147264686	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5698554	AGCACCCATGCCTTA[C/T]TAAATTTTTTTCTAT	54476
rs147333730	snp	A/T	0.110872	0.20771	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674280	TGATCCACCCACCTC[A/T]GCCTCCCAAAGTGTT	54476
rs147349291	snp	C/G	0.00557542	0.0525036	intron-variant	RNF216	GRCh38.p7	7:5686194	TGCTGCTGCACTCCA[C/G]CCTGGGTTGACAGAG	54476
rs147351931	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5627890	AGAGCATGCAGGCCA[C/G]TGCCTGATTTTTATC	54476
rs147365137	snp	C/T	0.0150606	0.0854603	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768527	CATTCTTTTCAAGTG[C/T]ATGAGAACATTCACA	54476
rs147368023	snp	C/G	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5765701	TAATCCCAGTACTTC[C/G]GGCGGCTGAGGCGGG	54476
rs147368789	snp	C/T	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5714983	GGCACTTACACTTAT[C/T]TATCAACATGGTCTC	54476
rs147399057	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754284	TGTCAGCTTCCCAAG[C/T]AGCTAGGACAACAGG	54476
rs147439272	snp	A/G	0.00557542	0.0525036	intron-variant	RNF216	GRCh38.p7	7:5687666	AAACCAACACAGAGA[A/G]ATTAAGTGCCCCCAA	54476
rs147440235	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5630946	CAGGTTTCTGAATCG[G/T]AACTTCTGGCAAACC	54476
rs147456957	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5642125	TACTATTACCTTAAT[A/G]AGTCACCTCTGTAGT	54476
rs147458267	snp	A/G	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5728944	CCCTCCTCACCCTCA[A/G]CCAAGGCCTTTAAGT	54476
rs147563765	in-del	-/A	0.0505692	0.150756	intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652267	AGGAAACAGAGGCTC[-/A]AGGGTTAGATTACTT	54476
rs147564353	snp	C/T	0.0142736	0.0832652	intron-variant	RNF216	GRCh38.p7	7:5653874	TCTGGCAGGCAAAGC[C/T]GGGCATGTTCAGTTC	54476
rs147580587	snp	C/T	0.00874735	0.0655527	intron-variant	RNF216	GRCh38.p7	7:5650909	CTGCCCAAATTGCCA[C/T]TGCCCACTTCATTTT	54476
rs147581864	snp	C/T	0.0535932	0.154675	intron-variant	RNF216	GRCh38.p7	7:5686382	CCACCCTGAAGGGGG[C/T]TGGGACAGAAAACAG	54476
rs147614583	in-del	-/AAT	0.121717	0.214577	intron-variant	RNF216	GRCh38.p7	7:5737523	GAATGATCAATTAAA[-/AAT]AATAATAATAATAAT	54476
rs147623466	snp	A/C/G	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5745617	TGTAAAAAGCAACAA[A/C/G]GGCAGGGCACGGTGG	54476
rs147623848	snp	A/T	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5778859	TGTGATTCTCCTGCC[A/T]CAGCCTCCCCAGTAG	54476
rs147627666	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5693247	TCACGCTATAAAGGC[A/G]GAGTTAGGTAGCTGG	54476
rs147640073	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5775983	CATGTTTTTAAAAAT[A/G]TCTATAAACGATTGT	54476
rs147652062	in-del	-/C	0.00716266	0.059414	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678124	TGTGGAGCCAAAGGG[-/C]CCCGGCTACATAAAT	54476
rs147669836	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667060	GATGCACCCGCCTCG[A/G]CCTCCCATATGCTGG	54476
rs147686054	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663143	CTTAGCTTATGCGTT[A/G]TTACTGCACTTTTAG	54476
rs147713718	snp	C/T	0.00517822	0.0506191	intron-variant, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711461	CAAGCAAGAAAAATG[C/T]TGACACAGTGGAAGA	54476
rs147733004	snp	C/G	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5734060	TAAAAGCTTAGGAGG[C/G]GAAAAAAATCTCCAA	54476
rs147757575	snp	C/T	3.36027e-05	0.00409881	missense, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712833	TTGGGAACGAACACG[C/T]GCAGCTGCCTTCCAT	54476
rs147771826	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5683551	CCACCTCATCAGAAC[G/T]CTCTGAACAGGTAAG	54476
rs147805116	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622329	CACTCACTGCAGTGG[C/T]GCACGGGTTTTGGAT	54476
rs147818992	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5724009	AGCACCTAAATTAAA[C/G]TGCTATACCTAAAAC	54476
rs147820300	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668973	TATCCAGCCGAAATC[C/T]AGTCATCTCCCCCAG	54476
rs147835129	snp	C/T	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5752017	ATAGTTAAACCTATC[C/T]CTGCTAAAAATACAA	54476
rs147871230	snp	A/G	0.000610959	0.0174673	missense	RNF216	GRCh38.p7	7:5715169	CCCCATAGCAGCAGC[A/G]ACACTCAATCAGCTG	54476
rs147879845	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5638953	TTTTTTCCCTACTTA[C/T]AATTTTTTTAAACTT	54476
rs147881383	snp	C/T	1.64738e-05	0.00286995	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741200	CCGGCCTTGGAAAAG[C/T]GGGCCCTGGGAATTC	54476
rs147896131	snp	C/T	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5635873	ATGGCTAGGCGATAA[C/T]TGTACCAAATTAAAC	54476
rs147896387	snp	A/G	0.00914312	0.0669923	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671668	AAATCAGCTGGGCGC[A/G]GTGGCGGGCACCTGT	54476
rs147924656	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5733015	CCTGCTTAAAATGGC[C/T]AGACGGTTCCATCTG	54476
rs147926708	snp	G/T	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5684072	GTGATGGTGGGACCA[G/T]TGTTTCCACAAGCTG	54476
rs147941428	snp	A/G	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5766027	TCACACTTGTAATCC[A/G]GGAAACCAATCCTTG	54476
rs147976207	snp	A/G	0.00557542	0.0525036	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664543	ATCAGGATAAAAGGA[A/G]CTCACAAACAGTAGA	54476
rs147990487	snp	A/G	0.0295035	0.117819	intron-variant	RNF216	GRCh38.p7	7:5749371	GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAA	54476
rs148026502	in-del	-/AACT	0.00676609	0.0577691	intron-variant	RNF216	GRCh38.p7	7:5743438	GTGAATGGTTAAATA[-/AACT]ATTACTTATTTGTTC	54476
rs148052049	snp	C/T	0.00993419	0.0697739	intron-variant	RNF216	GRCh38.p7	7:5633042	TGGAGTGCAGTGGTG[C/T]GATCTCTGCTCACTG	54476
rs148064983	snp	A/G	0.0146672	0.084371	intron-variant	RNF216	GRCh38.p7	7:5738149	TCTGCAGATTAGAAG[A/G]AGGGGAAAGAGTATA	54476
rs148101703	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5709455	TGAACTGTTCTCTCT[A/G]TGGGAAAAAGAGGGT	54476
rs148105914	snp	A/C	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5630287	CTCTGGGGCTCCAGA[A/C]CTGGCTTGAGTGCAT	54476
rs148113247	snp	C/T	0.111576	0.20818	intron-variant	RNF216	GRCh38.p7	7:5760287	TTTGGCAGGCTGAGG[C/T]GGGCGGATCACCTGA	54476
rs148119231	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5719724	ATCTAGAATTTTGGT[A/C]AAAAATAATCACTTC	54476
rs148148902	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5728231	CTGGAGACCCTTGGT[A/C]TACCTTAGGTTGCCT	54476
rs148165884	snp	A/G	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5756120	CTCGTGATAGTGAGT[A/G]AGTCTTGAGGTGTCC	54476
rs148188033	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5693409	GGTATGGACCTCCAC[G/T]GTACTGAGGTACCAA	54476
rs148189063	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5636914	CCACACCATCAATCC[C/G]AGGCATGGGAAGCAA	54476
rs148200844	snp	A/G	0.0839998	0.186933	intron-variant	RNF216	GRCh38.p7	7:5776509	CTGAGGCAGGAGAAT[A/G]GCGAGAACCCGGGAG	54476
rs148204874	snp	C/G	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5725095	TTTTCTAACACCACA[C/G]AAAATTTTCCTCTCA	54476
rs148232680	in-del	-/CTAA	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5654860	TATATATTAGGGTGC[-/CTAA]CTATTACCCACCGAA	54476
rs148275656	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768056	CAGGATCAAGATGAT[C/T]TGCCGGTACTCTAAT	54476
rs148282284	snp	A/C/T	4.96266e-05	0.00498105	missense	RNF216	GRCh38.p7	7:5622917	GTTGTGCTCCAGGGG[A/C/T]ATGTGGATGGGACCG	54476
rs148307693	snp	C/T	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5705602	GGAAAAAATGAACCA[C/T]ATGCCCTTTAAAAAA	54476
rs148315378	snp	A/G	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5658587	TCTTGAGCCTGGGAG[A/G]TGGAGGTTGCAGTGA	54476
rs148343419	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5774789	TTGAGACGAAGTTTT[A/G]CTCTTGTTGCCCAGG	54476
rs148352106	snp	C/T	0.000923254	0.0214657	missense	RNF216	GRCh38.p7	7:5623018	GGAAGTTGTTGAACA[C/T]AGGCCGCACGGGAGG	54476
rs148357415	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753121	AGCAGCCCGTGCACT[G/T]AAGCATTAAGAGCCA	54476
rs148361634	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5701195	CTAAAGGAGAGCTGT[C/T]ATTTCTTATAGAATG	54476
rs148410632	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5706932	TTAATCCATTTAAAG[A/G]GTTGATTTTTGTGTT	54476
rs148416898	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5659706	TAGGGGAACAGGCTC[A/G]GAGTGTGGATTTGAT	54476
rs148428368	snp	C/G/T	9.90008e-05	0.00703503	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741046	CAAATGTTTTCCAAA[C/G/T]TGGGCTCTTGAGATT	54476
rs148433114	snp	A/C	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5691722	CCCGGCAGGGAGTCC[A/C]TCAGTACTAACTCTA	54476
rs148448168	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754371	TCTCACTATGTTCCT[A/G]TGCTGGCCTTGAACT	54476
rs148462363	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5704176	GGATTCCAGAGGACT[A/G]ATTCCAGCCATTCAA	54476
rs148467294	snp	A/G	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5625014	ACAAAACAGCTGTGC[A/G]GTTTGTGGGACTGAA	54476
rs148470361	snp	G/T	0.00953873	0.0683987	intron-variant	RNF216	GRCh38.p7	7:5656492	CCCTTGTGCCTTTCC[G/T]ACTGGGGGAAACCAC	54476
rs148499999	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750782	TACTTATGCCTCTCA[A/C/T]GTGGCAGGACAACGT	54476
rs148538727	snp	A/G	0.00478085	0.0486577	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671886	GTGAGGACACAGCAC[A/G]AAGACAGTCCTCTGC	54476
rs148575313	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5634951	GGGGAAAGAGTCTGG[C/T]GAGGTCCCCACCCCT	54476
rs148587513	snp	G/T	0.0236746	0.106192	intron-variant	RNF216	GRCh38.p7	7:5723514	TAGCCGGACTCGGTG[G/T]CGGGCACCTGTAGTC	54476
rs148591227	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666630	GGGATCCCTTTCACG[C/G]GGAGCTCTCAAGCCT	54476
rs148626128	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5688512	TATAAACAAAAAGCA[A/G]AAACTCCCCTCTTGT	54476
rs148627830	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5631761	ACAGCTAAAATCAGC[C/T]GTAATTCCTCACCAG	54476
rs148634146	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5761997	TCAGCTAAAGAAACC[C/T]CTGTGTGTTCTCCAA	54476
rs148642312	snp	A/C/T	0.000247068	0.011112	missense	RNF216	GRCh38.p7	7:5721061	TTGATTTTCTGCTCA[A/C/T]AGAACTCCTGCTCTT	54476
rs148656693	snp	C/T	0.0185938	0.0946107	intron-variant	RNF216	GRCh38.p7	7:5729206	GAAGGTATTACACTC[C/T]ATGTTTTTACGGTCA	54476
rs148672800	snp	C/G	0.00835141	0.0640778	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675266	TCCCTCTGCACACAC[C/G]CTAGGTTCTGCACAG	54476
rs148675517	snp	A/G	0.0142736	0.0832652	intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652351	ATGCCCTCTCTACCA[A/G]AAAGCAGGTTAATGG	54476
rs148677878	snp	C/T	0.00676609	0.0577691	intron-variant	RNF216	GRCh38.p7	7:5685997	GGAGGCTGAGGCGGA[C/T]GGATCATCTGAGGTG	54476
rs148685927	snp	C/T	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5757767	ACAAGGGAATCTTTT[C/T]GGAGTGATAGAAAAT	54476
rs148710454	snp	A/G	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5778047	CCCAAGTACTGCCTT[A/G]CAGGCTCCATCCCTT	54476
rs148725113	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5726085	TGTTCAAGGCTTGCC[C/T]GGGCAACATGGGGAC	54476
rs148748760	snp	C/T	0.00874735	0.0655527	intron-variant	RNF216	GRCh38.p7	7:5642517	ACTGTGCCTGGCCTA[C/T]TTTTTTTGAGACTCA	54476
rs148802076	snp	C/T	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5694672	AGGACCTGCCTGCCC[C/T]GGAGCAGAGATGTGT	54476
rs148803197	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5638493	AACTGCCCACTATGC[C/T]CAATTACAGTGTAGC	54476
rs148809597	snp	C/T	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5769548	GGCAACATGGTGAAA[C/T]GCTGTCTCTACCAAC	54476
rs148833951	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5650775	GTCTACTCGGATAAT[A/C]CAGATAACCTCCCCA	54476
rs148855794	in-del	-/GGT			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679192	TCACCCTCGGGTAGG[-/GGT]GGTGGTGGTGCGGTG	54476
rs148903480	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5696462	AACAAATTCACTGGC[C/T]GGTGGGAATGCAGCA	54476
rs148915566	snp	C/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5748941	GTGTCTCCGTGTCTA[C/T]ATATGCGTTATGTGT	54476
rs148937358	snp	A/C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5629934	GGACTTGGGATAAGT[A/C/G]ACAGATGGGGTATTG	54476
rs148953678	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5660908	CTAAAACTCCTGCTT[C/T]TCACAGTACTAGCTC	54476
rs148966920	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5745132	TAATATTAGCAAATG[G/T]AATCCCCAGCAGCAC	54476
rs148970395	snp	A/G	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5755553	AGGATTTCTAATTGC[A/G]CAGATAAGTTTTGCA	54476
rs148973876	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5705232	GCATTGTAAAAACAC[C/G]TACACACTGGATGTC	54476
rs148989996	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5625664	ATTTCCTTCACTAAA[C/T]GTGCACTGCATGCCT	54476
rs149005104	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5716461	TGTAAACTTTCCTTT[A/G]TGAGTGTATCTGATG	54476
rs149012430	snp	A/G	0.000249143	0.0111584	synonymous-codon	RNF216	GRCh38.p7	7:5623088	CTGTGGCTGTGGCAG[A/G]TTCTGCGGAACGGGC	54476
rs149024894	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5752504	AAATCCATATAAAAA[C/T]TTAAGTGCAAGAATA	54476
rs149040259	snp	A/C/T	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5680274	CCAACAGGGAAGTGG[A/C/T]TCCTTTGTCCCCCGC	54476
rs149111613	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5636862	ACAAGGCAGTGCATG[C/T]TATGGCACCCAAACA	54476
rs149112801	snp	C/T	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5724754	GATCTCTAGAAAAGT[C/T]GTAGTAAACGCCTTT	54476
rs149115129	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669234	CAAGATCTCTGATTC[C/T]GACACATAGTAAAGT	54476
rs149152152	snp	C/T	0.00835141	0.0640778	intron-variant	RNF216	GRCh38.p7	7:5632620	CATCTCTACTAAAAA[C/T]ACAAAAATTAGCCAG	54476
rs149159792	snp	G/T	0.000329402	0.0128294	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741581	GGCCACTTGGCTTAG[G/T]GAATTCAGAGATTCC	54476
rs149161834	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5690069	GTGGGTGGCTCATGC[C/G]TGTAATCCCAGCACT	54476
rs149177984	snp	A/C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5773146	CTCATTTGAAATAAT[A/C/G]ATATTGATGTTATTA	54476
rs149200716	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5654295	ATACTATATGTGTAC[G/T]ATCTAATAAAAAGAA	54476
rs149217704	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5686562	ATCTGTACAATGCAC[A/G]CCAGTGTTCCTAAAC	54476
rs149267220	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5691279	GGCAGCATTTGACTG[C/T]TAGGACACTGTCTTG	54476
rs149268282	snp	C/T	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5634449	AGATCGCCTGAGCAA[C/T]GGCAGACCCTTAGCC	54476
rs149273970	snp	C/T	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5644354	CTTGTTATTTTCCAT[C/T]GCTTTCATTATAGTC	54476
rs149280034	snp	C/T	0.0107246	0.0724382	intron-variant	RNF216	GRCh38.p7	7:5774465	ATTAATTTTAAAAAA[C/T]AAAAACTTTTTAAAA	54476
rs149291024	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5655698	AAACACCAGGCTGGG[A/G]AGTTTAACATTTGGA	54476
rs149318854	snp	A/T	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5737227	ATTACCTTACCCCCA[A/T]CCCAGTGCTCTCTGA	54476
rs149319048	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5687345	AGGTTGCAGTGAGCT[C/G]AGACTGCGTCACTGC	54476
rs149328847	snp	A/C/T	6.82e-05	0.00583912	synonymous-codon, missense	RNF216	GRCh38.p7	7:5641376	AGTCATTTTTTCTTC[A/C/T]CTGAAATAAGAAAAC	54476
rs149335251	snp	A/G	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5771660	AAAATTTAGCCAGGC[A/G]CAGTAGCGGGCACCT	54476
rs149340965	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5709365	CTCTGGAGAGCCAGC[A/G]TCACAAATTCCCCAG	54476
rs149348968	snp	A/G	0.124491	0.216211	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781140	TCACAGGCACGGCCC[A/G]CCTCCCGCCGCTCCT	54476
rs149357899	snp	A/C/G	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5651619	GAGAGAAGAGAAAGA[A/C/G]ATTTCAGTATTACTT	54476
rs149426232	snp	A/T	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666258	ACACACATTAAGTGT[A/T]ATATACAGTTAAGAC	54476
rs149439605	snp	C/G	0.00676609	0.0577691	intron-variant	RNF216	GRCh38.p7	7:5750707	TTCACAACAGCAAAC[C/G]ACATTGGAGCAAGAC	54476
rs149444097	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5698153	AAGCAAATGCCAATC[C/G]TAGTTTTAAAATCCT	54476
rs149450886	snp	A/G	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5631555	ATTTCCTTGCCTGAC[A/G]TGTTTTCTCCTGACA	54476
rs149479001	snp	A/C/G	0.00239401	0.0345304	intron-variant	RNF216	GRCh38.p7	7:5720863	TATGAAACCACAAAC[A/C/G]TAAGTATTATGACAA	54476
rs149480211	snp	A/G	0.0142736	0.0832652	intron-variant	RNF216	GRCh38.p7	7:5661808	ACTCTGCTCAAACAA[A/G]AACAAAAACAAAAAA	54476
rs149486237	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673647	ATCTGGAGAATAAAA[A/C]ACCCCATATCATCAC	54476
rs149494683	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5746552	CTTGCAGGCTTAGGT[A/G]AGGGAGGCCTCAGGT	54476
rs149498380	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5757306	ATACAGGGATTAGCT[A/T]ATCTTCTCAGTGCAC	54476
rs149500909	snp	A/G	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5685949	AAATTCCGGCCGGGC[A/G]CGGTGGCTCACACCT	54476
rs149516044	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767651	TGCCACCCAGGCTGA[A/G]GTAATGGTGCGATCT	54476
rs149517561	snp	C/T	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5627319	CACCAGTCAGGACCG[C/T]GCTGGACGCTGCAGA	54476
rs149527293	in-del	-/C	0.132751	0.2208	intron-variant	RNF216	GRCh38.p7	7:5722846	TCCAACATGGTGAAA[-/C]CCCCCCAGGCATGAT	54476
rs149550027	snp	G/T	0.00557542	0.0525036	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753867	ATGCGTGGTGGCGCA[G/T]GCCTGTAATCCCAGC	54476
rs149555724	snp	C/G	0.0154538	0.0865337	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681532	AGCCTCTAGGGCTAG[C/G]CAGGACCTGTAGCAC	54476
rs149635411	in-del	-/AAAAC			intron-variant	RNF216	GRCh38.p7	7:5705918	ATCTCAACAAAAACT[-/AAAAC]AAAACAAAACAAAAC	54476
rs149655511	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5682630	CAGGCTGATCTTGAA[C/T]TCCTGACCTCAAATG	54476
rs149737920	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5779334	AAAATCTAAAGCCTC[C/G/T]AATGAGGTTTGCCAG	54476
rs149754825	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5727261	TGTAGAGAAACTTAT[C/T]AAAGGAGCTGTTTAT	54476
rs149758339	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5650398	AGAATGAAGGCTGTG[C/G]TTTGTAAGTAATTCT	54476
rs149760504	snp	A/G	0.00835141	0.0640778	intron-variant	RNF216	GRCh38.p7	7:5660757	TAATTTTTTGTAGAG[A/G]TGGGGTCTTGCCATG	54476
rs149778410	snp	A/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5692608	GAAAGGCAGAGCTGC[A/T]CAGTTCCAGCTCCTT	54476
rs149799056	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5646231	TAAATTAGCCGGGCA[C/T]GGTGGTGCATGCTTG	54476
rs149806763	snp	C/T	0.00874735	0.0655527	intron-variant	RNF216	GRCh38.p7	7:5775525	CAGATTTGGGGGTCA[C/T]TAAAGACTTTCAAAT	54476
rs149808991	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5703324	TGAAGGCCGTGCTCA[G/T]CACAGGAGTCAGCTG	54476
rs149812076	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5716171	TGCTGGAATTACAGG[A/C]ACGAGCCACGGTGCC	54476
rs149828912	snp	C/T	0.0178098	0.0926698	intron-variant	RNF216	GRCh38.p7	7:5738871	ATCATAATTCTATAA[C/T]CATGCAGTATTCCAT	54476
rs149833669	snp	C/T	4.95495e-05	0.00497718	missense	RNF216	GRCh38.p7	7:5623062	GGGTGCGCGAAGGCA[C/T]AGGGTGGCATCTGTG	54476
rs149840029	in-del	-/G			intron-variant	RNF216	GRCh38.p7	7:5635893	CAAATTAAACTGGCT[-/G]GTAAAAGCCCTAGGG	54476
rs149867866	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5710705	CATTGCTGCCACTCC[C/T]GGGGCCTAGAACATT	54476
rs149876020	snp	A/G	0.0150606	0.0854603	upstream-variant-2KB	RNF216	GRCh38.p7	7:5783291	TGTGCCACCACGCCC[A/G]GCTAATTTTCGTATT	54476
rs149917346	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5625609	ATGAGTGATTTCCCC[A/C]CACAATTGTTTGTGA	54476
rs149957776	snp	C/T	0.0023933	0.0345097	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621662	CCAGCCTCTCAGAAC[C/T]CCATGGCAACACGAC	54476
rs149964919	snp	C/G	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5752429	GGAAGATTTGTTTTG[C/G]ATTACGCAAACTGAT	54476
rs149965776	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5699611	CTCTGCATTACCAAG[A/G]ATATTCACAGTCCAT	54476
rs149969612	snp	C/G	0.00398564	0.0444627	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679778	TGAGTGCCTGCATTT[C/G]TAACAACTGGCCCTG	54476
rs149987343	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5722034	TCAGGCAATCCTCCC[A/G]CCTCAGCCTCCTGAG	54476
rs150003662	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663089	GAAACCCAAATGACC[C/T]GGGAAGAGCTGGCAC	54476
rs150011164	snp	A/C/G	0.000411749	0.0143427	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741414	TGTCTCTGAGTCTTC[A/C/G]GATGACTGGTTCTGA	54476
rs150016260	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5748298	AATTCCACCTCATTT[C/T]AATGCTGAAACTCTA	54476
rs150021181	snp	C/T	0.0170251	0.090679	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674953	AGTGAGCTGAGATCG[C/T]GCCACTGCACTCCAG	54476
rs150025602	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5686442	GAGTAAATGATGTGC[A/G]GACAGTCACACAGTG	54476
rs150027526	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5629567	GAAGCGGCGTCTTGC[A/G]CCTGTAATCCCAGCA	54476
rs150042182	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5718911	TGATTGCCTGCCTTG[C/G]CCTCCCAAAGTGCTG	54476
rs150057973	snp	C/T	0.0142736	0.0832652	intron-variant	RNF216	GRCh38.p7	7:5638054	ACACCCTCTCCTTTG[C/T]CGCAGTCCCCACTAT	54476
rs150090462	snp	C/G	0.00835141	0.0640778	intron-variant	RNF216	GRCh38.p7	7:5722979	CAACAAAAAAAATCA[C/G]TTTTTGGTATTATGA	54476
rs150093971	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5643965	TGTGTTTTTGTGCCT[C/T]TTTTCACTTAGTGTG	54476
rs150129599	snp	A/C	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5630713	ACTCTTATAAAGCGC[A/C]AAGCACAGTGACAAC	54476
rs150139065	snp	G/T	0.0197687	0.0974348	intron-variant	RNF216	GRCh38.p7	7:5687160	CAGCACTCTGGGAGG[G/T]TGAGGTGGGCAGATC	54476
rs150141591	snp	C/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5771539	CAGTGGCTCATGCCT[C/G]TAATCCCTGCACTTT	54476
rs150142187	snp	C/G	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5720031	AGGTGAAACTGGTGT[C/G]TCTTAAAAATGTAAG	54476
rs150144528	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5695922	GCAGAGGTGCCACAG[A/T]AAACATGTTTCCCGT	54476
rs150148326	snp	A/G	0.000214156	0.0103456	synonymous-codon	RNF216	GRCh38.p7	7:5641283	CATCTGGGCACCACA[A/G]CGGCAAGACATGCGG	54476
rs150181126	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5685249	TGGAGACAGTGAGCA[C/T]GAACAAAACCATCTC	54476
rs150190697	snp	A/G	0.0263992	0.111815	intron-variant	RNF216	GRCh38.p7	7:5734124	AATAGGAAGGTGGAT[A/G]CCAGGGTGTGGGGCA	54476
rs150193409	snp	C/T	0.00993419	0.0697739	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767124	ATTAATAGCCTATAG[C/T]AGACCAACCCTTTGC	54476
rs150262878	snp	C/T	0.0287284	0.116357	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780580	CAAATGCCTGTAATC[C/T]CAGCTGAGGCAATCC	54476
rs150281306	snp	A/C/T	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5651469	ATTCGTGAGCTCAAG[A/C/T]GATCTACCTGCCTTA	54476
rs150296339	snp	A/C	3.30759e-05	0.00406655	missense, intron-variant	RNF216	GRCh38.p7	7:5741754	TCTCCCAACCTTTTC[A/C]GATCTTGCCACTGGG	54476
rs150298353	snp	A/C	0.0225045	0.103662	intron-variant	RNF216	GRCh38.p7	7:5745935	GAGAACACTTACTCT[A/C]CATTTTGGAATGAAG	54476
rs150299579	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5693953	TGGAATTCACTTGCT[A/G]TTGTTGACCAAAAAA	54476
rs150314357	snp	A/G	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5776674	TAGCCATATCAAGCT[A/G]AAGTGAGAGACGTGT	54476
rs150332965	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5705062	AGCTAATAATAATCT[C/T]CCTGATGGGCACCTT	54476
rs150335150	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5647522	GATTTTCTGTACAGA[C/G]AGGGTCTCACTTTGT	54476
rs150346784	snp	A/C/G	0.00036234	0.0134552	synonymous-codon	RNF216	GRCh38.p7	7:5729510	GAGCACTTTGAAGTC[A/C/G]GCCATGAGGAGGTCA	54476
rs150347267	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5717288	AACCTGGGAGGCAGA[A/G]GTTGCAGTGAGCCGA	54476
rs150364829	in-del	-/A	0.181022	0.240296	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675485	ACGAAAAATAAATTT[-/A]AAAAAAATTAGCTGA	54476
rs150400749	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5763952	TAAGCACCTTGGGAG[A/G]CCGAGGCAGGCGGAT	54476
rs150402430	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713540	CAGGCAGGAGGCAGA[A/C]TGAATCACCCCAGGT	54476
rs150439339	snp	C/T	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5626333	ATGTGAATATCAAGG[C/T]AGATGCTATCAACTC	54476
rs150453303	snp	C/T	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5758640	TTAATGACCGCCCTG[C/T]TGGGTTTTGGACTTG	54476
rs150492840	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681421	GAAACAACTGTGGAT[C/T]ACCAAGTCCCCAGCA	54476
rs150494013	snp	A/C/G	0.00352457	0.0418319	missense, synonymous-codon	RNF216	GRCh38.p7	7:5623040	CACGGGAGGCAGGGG[A/C/G]AAGGGTGGGTGCGCG	54476
rs150497607	snp	A/G	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5633444	GCTGGGCCTGGTGGC[A/G]TGCACCTGTAATCCC	54476
rs150504067	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5765380	GAGGTAAGAGAATTG[C/G]TTCAGCTTGGAAGGT	54476
rs150581301	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682310	GTTACCCTCACACCC[A/G]TCCCTCTAAAAGGGC	54476
rs150597231	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5625250	GAGGTCCTCCAGGAG[C/T]TGAGAGCAGCCGAGC	54476
rs150626197	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5775337	ACTTCCTCGTGACCA[A/G]AATGCTTGAGGCTGT	54476
rs150648973	snp	C/T	0.00557542	0.0525036	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677967	ACTGGAGCAGTAAGA[C/T]CACAGTGATCTTTCC	54476
rs150661307	snp	A/G	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5738837	ACAGGTAGTATCAAC[A/G]CTTAGAAACAACTCA	54476
rs150664775	snp	A/G	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5689067	AAAGAACAGGCTGCC[A/G]ATTCTGTGAAACAAA	54476
rs150670281	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5697921	AGAGAAGGGCAAAAG[C/G]ACAAGCTGTAGTCAA	54476
rs150671235	snp	A/C	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5641772	GAGCATGGTGGTGCA[A/C]GCCTGTAATCCCAGA	54476
rs150677265	snp	C/G	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5772285	AATTCTGGGAAGACA[C/G]TAGTAGTAACAGCAG	54476
rs150686204	snp	C/G	0.0158469	0.0875917	intron-variant	RNF216	GRCh38.p7	7:5728531	GTGAGCCGAGATTAG[C/G]CCACTGCACTCCAGC	54476
rs150718222	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5661789	GCCTGGGCGAGACAA[C/T]GAGACTCTGCTCAAA	54476
rs150725128	snp	C/T	6.60044e-05	0.00574438	missense	RNF216	GRCh38.p7	7:5622948	AAGTCATAGTTGACC[C/T]GCACGTTGGGCAGAG	54476
rs150767417	in-del	-/TAA			intron-variant	RNF216	GRCh38.p7	7:5737534	TAAAAATAATAATAA[-/TAA]TAATAATAATAAATA	54476
rs150776265	snp	C/G	0.00199481	0.0315187	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621362	TATTTTTAGTAGAGA[C/G]GGGGACTCAAACTCC	54476
rs150806226	snp	A/T	0.0103295	0.0711199	intron-variant	RNF216	GRCh38.p7	7:5653371	CGAGGTGGGCGGATC[A/T]CGAGGTCATGAGGTC	54476
rs150834804	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5747937	TTTTGAGCCACTGTG[C/T]CTGCCCTGACCCTTA	54476
rs150837969	snp	A/C/T	0.00796258	0.0626796	intron-variant	RNF216	GRCh38.p7	7:5778338	ACTCTATTCATTGTT[A/C/T]GGTTCTTTGCTTTCT	54476
rs150842751	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5757050	ATCATGTAATTCAAA[A/G]TATCTTCTAATTTTC	54476
rs150843286	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5706286	CCAATTAACACATTT[G/T]TAAGTGTACAGGGTC	54476
rs150874270	snp	C/T	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5718375	GACAAAGCGAGACTC[C/T]GTCTCAAAAAACAAA	54476
rs150875683	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5660111	GAACACGTGCCACCA[C/G]AGCTAAATTTTGTTA	54476
rs150881855	snp	A/G	0.000346824	0.013164	missense, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712742	TCGGCGTAGGCTGCC[A/G]CAACCTCCTCCTCGG	54476
rs150881970	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670628	GCTTAATCTCCACCC[C/T]TACTGCTTCATTAGT	54476
rs150890759	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5743190	TGCTTGAACCAGGGA[C/G]TCAAGAGGTTGCAGT	54476
rs150932064	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676081	GTGCAACGCGATCTC[A/G]GCTCACTGTAACCTT	54476
rs150948585	snp	A/G	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5707861	CTCCCAAGTAGCTGC[A/G]ATTACAGGCGCACGC	54476
rs150950298	snp	C/G	0.00835141	0.0640778	intron-variant	RNF216	GRCh38.p7	7:5760380	AATTAGCAGGGCGTA[C/G]TGGCACATGCCTGTA	54476
rs150965109	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5628829	CACCCAGCTGGAAGA[C/T]TTCTTTCTTAATTTG	54476
rs150981970	snp	C/T	0.0205511	0.0992634	intron-variant	RNF216	GRCh38.p7	7:5639658	TAGAGACAGGTTTCA[C/T]CATATTGGTCAGGCT	54476
rs150985450	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672012	TAAGCCCCTAGTCTG[C/G]TATTTTGCTAAGGCA	54476
rs150996218	snp	A/G	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5726979	CGCCTGCAAGAGAAG[A/G]AGGAAGAGTGGGAGC	54476
rs151000119	snp	C/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754536	AAGACACACGCTATG[C/G]GGGATCATTCTGAAG	54476
rs151031390	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5716489	ATGAATGTCAGGTAA[C/T]GATTTTTAACAGGAA	54476
rs151031645	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5692332	GTAACAACTTTATTT[A/G]CTGATTTCACAACCC	54476
rs151034318	snp	A/G	0.00557542	0.0525036	intron-variant	RNF216	GRCh38.p7	7:5635373	AGCTGTGGAAGCTGG[A/G]TGATGGGACAATCTG	54476
rs151107691	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5684816	TCTAGTAAACCAAAT[A/G]ACATGCCTCACATTT	54476
rs151143662	in-del	-/TAA	0.0298908	0.118541	intron-variant	RNF216	GRCh38.p7	7:5690853	CACCAGCCTGACACT[-/TAA]TAACACATACGCACA	54476
rs151144599	snp	C/T	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5647025	CCCATGTGTTACTCA[C/T]TGCCTCAGGCAGCTG	54476
rs151175170	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5762730	AAAAATTAAAAATAC[A/G]GTATGCGTAAGAATG	54476
rs151176747	snp	C/G	0.0142736	0.0832652	intron-variant	RNF216	GRCh38.p7	7:5657379	TCGAGACCAGCCTGA[C/G]CAACAGGGAGAAACC	54476
rs151197918	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5643401	CAGGAAACACAGCCC[C/T]GCAGGATGTGCTCCC	54476
rs151207649	snp	C/T	0.00953873	0.0683987	intron-variant	RNF216	GRCh38.p7	7:5698978	AAGCAGCAAAGCAAA[C/T]CAAAACAATGAGAGC	54476
rs151209659	snp	G/T	0.00279162	0.0372561	upstream-variant-2KB	RNF216	GRCh38.p7	7:5783068	CGGGCATGGTGGTGC[G/T]CACCTATAGTCCCAG	54476
rs151211079	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5729292	ACGATGAGCAAATAC[A/C]CATCTATTTATCTTC	54476
rs151245222	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662985	CACACCCCCTATGCC[C/T]TCAATGGCACAACAT	54476
rs151249501	snp	C/T	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5694859	GTCTACTAACTACTC[C/T]TGTTTTGATTTTGAA	54476
rs151280655	snp	C/G	3.29527e-05	0.00405898	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741083	TTGGAAAGGCTGGAC[C/G]TGGCTCTTCATCATC	54476
rs151284170	in-del	-/ACCATC	0.0322114	0.122752	intron-variant	RNF216	GRCh38.p7	7:5640685	AATTGTTAATATTAA[-/ACCATC]ATTGCATTTCTAGAA	54476
rs180675993	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5717734	TGACTGCCAGGATGC[A/C]TGGTTAAATGAAAAA	54476
rs180714044	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5763068	AACTCTGGGGATAGG[A/T]AACAGAGAAATATTT	54476
rs180718003	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5695405	GCCCGGCAGAAGCGC[A/C]ACATCGCCTTCCTCT	54476
rs180724374	snp	A/G	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5749002	AGAACTCTGATAATC[A/G]GTTTAAGGAAAAAGG	54476
rs180731362	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643299	GTGGTGACTACCTAG[C/T]CAGTAATATAAAAGT	54476
rs180732644	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5655441	CATCTCTACTAAAAA[C/T]ACAAAAATTAGCTGG	54476
rs180732938	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781071	ACTTTCGCGGAACAC[A/G]CGCTCCAGATGTGAG	54476
rs180738359	snp	A/G	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768179	AAAATTACCAGGTGC[A/G]GTAGCTCATGCCTGT	54476
rs180746712	snp	A/C	0.00398564	0.0444627	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668781	TGTTGCCTGCCCTTC[A/C]AGGGCTTCATGCCCT	54476
rs180750297	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5686326	TCTGACACCTCTGTC[A/G]AAGAGCCCTTACCTG	54476
rs180753553	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5755561	TAATTGCGCAGATAA[A/G]TTTTGCATGTTTTTG	54476
rs180759840	snp	G/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5702705	CAAGAAGTCTGTGAT[G/T]AATAGATTCACTATG	54476
rs180760791	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5740598	TTTAAATGTAAACAG[A/C]CACAAGGAGCTAGTA	54476
rs180768690	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5730457	AAGATATGGAGAATT[C/T]GTTCAATTCTTTGTG	54476
rs180784484	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5776673	ATAGCCATATCAAGC[C/T]AAAGTGAGAGACGTG	54476
rs180882523	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5646961	GGTTTTTCTGAGCAT[A/G]TGTTGAGCCCTAGAC	54476
rs180886348	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622706	ACTCTTCCAGGAGCA[C/G]TAGCCCTTCTAGGAA	54476
rs180890648	snp	C/T	0.00557542	0.0525036	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665044	CTCAGGTGATCTGCC[C/T]GCCTCGGCCTCCCAA	54476
rs180893150	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5639705	CCTCAGGTGATCCAC[A/C]CGCCTTGGTTTCCCA	54476
rs180896340	snp	A/C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5656996	CAGGCCAAAGTCACC[A/C/G]GGTTCTGTGTTTGTT	54476
rs180902764	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671601	AGAGGTCAGCAGTTC[A/C/G]AGACCAGCCTGACCA	54476
rs180905225	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5689376	TTAAAAAAAAAAAAA[A/G]AAAGAAAGAAGAAGA	54476
rs180911797	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5706619	CCATTCATCTGTTGA[C/T]GAACATGTCAGTAAG	54476
rs180928871	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5652866	CACAAGGAAAAATTT[C/T]TCTCCCTAGATCAAA	54476
rs180950611	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681840	CCCAGAAAAGGAGGA[C/T]AGGAGGTGAAAAGGC	54476
rs180976233	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5751388	GACTAAGTGTGTGCA[C/G]TAGACCCCAAAAGAC	54476
rs180989340	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5630539	GTGTATCACCATGCC[C/T]AGCTAATTTTTAATT	54476
rs181006004	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5726720	AAAAATTAGCTGGAC[A/G]TGGTAGCAAGCGCCT	54476
rs181018368	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5738144	TCACCTCTGCAGATT[A/G]GAAGGAGGGGAAAGA	54476
rs181025005	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5778298	AGCTAAACTACTCTT[C/T]TTCACTGCCTCTTGG	54476
rs181028614	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5697379	ATCTGCTGAACGAAC[A/G]ACCAGACTTCAACCA	54476
rs181029513	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5714171	TTTCACCATGTTGGC[C/G]AGGCTAGTCTCGAAC	54476
rs181116252	snp	G/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677306	CTCTACTGTATGGGT[G/T]GTCTGGGCAATGCCA	54476
rs181127415	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5693118	CTATGGTATATGCTA[C/T]GGGTTGGCAAACTAC	54476
rs181160880	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5724626	TTTCTTTTAGAGCCT[A/G]AAAAGTTCATAGTAA	54476
rs181173016	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711385	TTTGAAAATGGCAAA[A/C]GGTGTGTGTGTGGGG	54476
rs181190238	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5661861	GAGGGTCCAATTAAT[C/T]TGGTCGAGGTCACAG	54476
rs181207014	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5701676	GCATAAGTGGGTTTA[A/T]TATCAAAATCCCTTG	54476
rs181230522	snp	A/T	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5762530	AAATAAATAAATAAT[A/T]AAAATACAAAAATTA	54476
rs181233668	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5748740	TTATTAAGTAGTACT[A/G]AGTAGTTAAGGCTTT	54476
rs181245822	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5740288	CCCGCCACCACGCCC[A/G]GCTAATTTTTAATTT	54476
rs181248704	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5642638	ACCTGGCTTTCATGC[C/T]CGGCCATTTTTTGTA	54476
rs181252082	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5626339	ATATCAAGGTAGATG[C/T]TATCAACTCTCTAGA	54476
rs181256855	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5655113	CATGGGTCTTCCTCA[C/T]AAGGGAAGAAACCCC	54476
rs181257844	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5635800	TGAATGTATTAACAT[C/T]TATAAATGTTAGGCT	54476
rs181264673	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5717532	GCCCAAAGATGCAAC[A/T]GGGCAGAAACAGGGA	54476
rs181267111	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5755100	GAAAGGAGAAGAGAG[A/G]AGGAAAGGAAGGAAA	54476
rs181277611	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5685545	TGAACTACATCAAGG[A/C]AAATTCTATTACTTT	54476
rs181317063	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5730320	CTAGTACCAGTGGTA[A/G]GTATATAAATGATCA	54476
rs181344247	snp	C/G	0.00557542	0.0525036	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668349	CTGCCTCAGCCTCCC[C/G]AGTAGTTGGGACTAT	54476
rs181365534	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5650696	TCAAGTCCTTCTCAC[A/G]TTTGTTTGACTCTTC	54476
rs181368483	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5726486	TGCTGGAGTTCAAAA[G/T]CCTTCCACTGGTGAG	54476
rs181376738	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713809	ACCATGTGTCAAACA[A/G]TAAGTTCATTAAACT	54476
rs181400106	snp	A/G	0.0158469	0.0875917	intron-variant	RNF216	GRCh38.p7	7:5776514	GCAGGAGAATGGCGA[A/G]AACCCGGGAGGCGGA	54476
rs181414224	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621816	CAGGAGGCGAGGAGG[A/G]TGAGTGGGGACATGG	54476
rs181418523	snp	C/T	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5632010	GAGTGGCTGGACCAC[C/T]AAGGTGGGCAGTGTG	54476
rs181421622	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5777978	AATCAACGTTTTCAA[C/T]GATCTTTTTAGAACT	54476
rs181422021	snp	A/G	0.00199481	0.0315187	intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652317	TGGGGTGGCTCAAGC[A/G]TGTTCTTCCGACAAC	54476
rs181423075	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5647762	ATCAGCTACCAAGAC[C/T]TGTTGATTTTACATC	54476
rs181428169	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5657741	TCCTCCCCACCCATA[A/C]GCCCAAATGACATAC	54476
rs181431108	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5697252	CGCTCATGCAGAGCC[A/G]CATGTTCCTCACAGC	54476
rs181434202	snp	A/C	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672762	TCCTGGTGAGCAGCG[A/C]AAGGTAGAGGATGGA	54476
rs181440498	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5764838	TTGGGAAGCCAAAGC[A/G]GGACAATCACTGGAG	54476
rs181441826	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5689984	AGGAGGGCAGGTAAC[C/T]CCCCTTATTTGCCGA	54476
rs181442005	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5751051	CCGAGGAGCAGCCTC[C/T]ACCCAAACTCTGGGT	54476
rs181448944	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5737685	AGCACCTGGAAAGGG[A/G]CCCTTCCTTCTCAGC	54476
rs181522383	snp	A/C	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680744	AGGCACCCCAGACAA[A/C]AGATGTCTGAAGCAC	54476
rs181523935	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5759064	GCACAATCCGTTCTG[G/T]TTGCAACAGTGAGTT	54476
rs181536210	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5733349	AGCAAGTCCCTAAAA[A/G]TAAGTACACGTGTGA	54476
rs181554267	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5635017	CCTATGGGCACCTAA[C/T]GACCATGTATTTGTG	54476
rs181554835	snp	C/G	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5639351	AGAGCTGCTAGCCCA[C/G]CCCTGGGCTGTTCAT	54476
rs181563968	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5650397	CAGAATGAAGGCTGT[A/G]CTTTGTAAGTAATTC	54476
rs181566999	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5661479	CAGCAACTCTACAGG[G/T]AAGTACTGGAGAATT	54476
rs181573312	snp	C/T	0	0	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676837	TCTCTGGTCATTGTC[C/T]CAGGCTAGATTCAAG	54476
rs181577485	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5692691	TTTTTAGGTGGTAAA[A/G]TAAGCCTTCCAACAC	54476
rs181622667	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5707069	CTTTGCACCCTTGTT[A/G]AAGATCAGCTGATCA	54476
rs181644907	snp	A/C	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5771689	CTAGTCCCAGCTACT[A/C]AGGAGGCTGAGGTGG	54476
rs181652669	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664682	TGGAAGGCCAGTTGC[C/T]GCCCAAGGGTAGGCT	54476
rs181674019	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5744940	TCGCGCCATTGCACT[C/T]CAGCCTGGGTGACAG	54476
rs181687258	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5740635	ATATTGGACAGCATA[A/G]GTCTAGGTAATTCAA	54476
rs181692020	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5730888	TTGCTTCAAATGCAA[C/T]GGTTGAAGAATATAG	54476
rs181698703	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5718256	CATGGTGGGGCGCAC[C/T]TGTAATCCCAGCTAC	54476
rs181702620	snp	A/T	0.021333	0.101051	intron-variant	RNF216	GRCh38.p7	7:5722565	CCGGCTAATTTTTTG[A/T]ATTTTTAGTAAAGAC	54476
rs181742009	snp	C/T	0.00914312	0.0669923	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782005	TGCAAATATATTCTG[C/T]GGATTTCCTGTGGGC	54476
rs181759038	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5756848	ACCATGTCGCCCAGG[C/T]TGGCCTCGAAATCCT	54476
rs181760732	snp	G/T	0.00914312	0.0669923	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768854	TTTTAGTAGAGACAG[G/T]GTTTCACCATGTTAG	54476
rs181799229	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5641685	GCATAGTGCCCAGTA[C/T]TCAGCATTTAGAAAA	54476
rs181842000	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5776258	AAAGAACTCAGAGTC[C/T]CATCAATCAGAGAAT	54476
rs181845931	snp	A/G	0.00716266	0.059414	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5621037	GGCAGTCCAACAGGT[A/G]TGGGCGCCAGCAAGG	54476
rs181846679	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5748487	CTGGTCTTGAACTCT[C/T]GGCCTTGGCCTCCCA	54476
rs181860949	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5724055	ATGAAATGAAGTTAA[C/T]GGGAAAATGTGAGAT	54476
rs181883707	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5702986	GCACCCTACATGATA[C/T]ACCTGTAAGGGAGCG	54476
rs181890573	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5744262	CTACATATGGATATA[C/T]AGCATTTTAAGTAAA	54476
rs181895581	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5714655	ATTCCCATACTGTGT[C/T]TGTTATGCTGGTGTC	54476
rs181900897	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5732969	AGCCAAAGTAGATTA[A/C]CTGCCATGTGGTTCT	54476
rs181954163	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5771292	ATTTAAACAGAAAGG[C/T]AAAATAAGTTTCTAG	54476
rs181956873	snp	A/G	0.00636936	0.0560724	intron-variant	RNF216	GRCh38.p7	7:5727431	CCTCATCTTGCACAA[A/G]CTCTTAGCAGCATTT	54476
rs181957141	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5758639	TTTAATGACCGCCCT[A/G]CTGGGTTTTGGACTT	54476
rs182006615	snp	A/G	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5689570	TCTCTTGGACTTCCT[A/G]CAAGTTTTTAAAGCA	54476
rs182014649	snp	A/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5656082	GAGACCAGCCTGGGC[A/T]ACATGGTCAAACCCC	54476
rs182052695	snp	A/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670348	CTGCTGCCCGACTGC[A/T]GAGGACCCAGCCATG	54476
rs182057349	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5687790	AGGACCTAAGTTTAA[A/C]GGTGCTAAGAGTTTT	54476
rs182063232	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5705049	CCCAGCATTTCTAAG[A/C]TAATAATAATCTCCC	54476
rs182069464	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5631703	TTTCTTTTCCTTATA[C/T]ATATTGATTAAAACA	54476
rs182073930	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5721935	CAATTTATGATTTTC[C/T]TTTTGGAGACAGAGC	54476
rs182089747	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5731936	TCTGCAGCCCCCGCC[A/G]GGGACCCACGTCAAA	54476
rs182095075	snp	A/G	0.0146672	0.084371	intron-variant	RNF216	GRCh38.p7	7:5657494	ATAGCTTGAACCCAG[A/G]AGGTAGTGGTTGCGG	54476
rs182095908	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5762129	ATAAAATTCATATGA[C/T]ACAACACAGTTAAAT	54476
rs182115440	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656290	ACAAACAAAGTGCTG[A/G]GATTACAGGTGTGAG	54476
rs182116063	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5735735	AACACCACCAATCTA[C/T]GGCCTGGTAGTGTAC	54476
rs182140662	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5686639	ATTTCTTTAAATACA[C/T]GTGAGCTGGGTTTGG	54476
rs182148190	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5765410	TGGAGGTTGCAGTGA[A/G]CTGAGATTGTGCCAC	54476
rs182152560	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5636385	AACAGAGAAAGAAAG[C/T]TACTGTTCACCACTT	54476
rs182155273	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5742071	TTTATTTTTGAGACA[C/G]AGTTTTCCTCTGCTA	54476
rs182164714	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5738437	AATATGGCTGGGAGC[A/G]GTGGCTCACACCTGT	54476
rs182249642	snp	C/T	0.00597247	0.0543191	intron-variant	RNF216	GRCh38.p7	7:5649470	GCTGTGATTGTGCCA[C/T]TGTATTCCAGCCTGG	54476
rs182272743	snp	A/G	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5627486	CACTCGGTGGTTCAC[A/G]CCTGTAACCCCAGCA	54476
rs182284413	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5734056	ATTTTAAAAGCTTAG[C/G]AGGGGAAAAAAATCT	54476
rs182288457	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672416	TGTTTGTTAAATTTA[A/G]TAACAAGAAGTGAAG	54476
rs182292875	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5723065	CTACTCGCTAGCTGT[A/G]TAACATCTGCCAAGT	54476
rs182301667	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5706777	CTGAAAGCATCTTAG[C/T]AGTCACTTGCCTGTT	54476
rs182323807	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5640840	AGGCTTTGGAATCAG[C/T]GTTATGCTGGCTTTG	54476
rs182335612	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673020	TCTTAACAAGAGACA[C/T]GGGGCAGGGGCAGGG	54476
rs182336630	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5654072	AAAAAATCATTCTGG[G/T]TGGAAAACACTGGAG	54476
rs182341121	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5690757	CTGCTGATGCTCCTG[C/T]AATACAGCCCACACT	54476
rs182344407	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5707426	CTTAATTTCTCTTTT[A/T]GGAGTGTTTGTTAGT	54476
rs182344586	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667022	ATGTTGCTCAGACTG[C/G]TCTCAAACTCCTGGG	54476
rs182350077	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5759524	TGTAAGAATACAGTA[C/T]ACAAAACATACAATA	54476
rs182364892	snp	A/G	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5745757	ACACAAAAATCAGCC[A/G]GGTGTGGTGGCACAC	54476
rs182385026	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5647132	GTGAAAAAAAAAAAG[C/G]GAAAAAGTTGCCTCT	54476
rs182413440	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5778516	AACTTAAGTTCCAAG[A/G]AGGCAGAACCAAAGT	54476
rs182420876	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5752497	GATTGTAAAATCCAT[A/C]TAAAAATTTAAGTGC	54476
rs182445248	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5736488	CCTCCACCTCCCAGC[C/T]GCCTGCCTTGGCCTC	54476
rs182446581	snp	A/G	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5628454	CTTTAATACAACTTA[A/G]AAGTTTTTTTTCTTT	54476
rs182447035	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5644981	AGGCACGTGCCACCA[C/T]GCCTGGCTAATTTTT	54476
rs182449856	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5651161	GTAAATGTGGCCACA[A/G]TCTAGTTACAATCAT	54476
rs182450589	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5778914	ACACCTGGCTAATTT[C/T]TGTATTTTTAGTAGA	54476
rs182452007	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5628019	GTTTCTGATACAGAT[C/T]GGCGGGGTCTGGAGG	54476
rs182460494	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677871	AATGTAAGGGAGCTA[C/G]AAAAACAGCTCTTTG	54476
rs182463095	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5656164	ATCCCAGCTACTCTG[C/G]AAGCTGAGACAGGAG	54476
rs182465460	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669687	CACTTGAGGTCAGGA[A/G]TTTTGAGACCAGCCT	54476
rs182487068	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782883	GTACACCTTCAAGTA[A/G]AGATATCAAGTCAGT	54476
rs182517366	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5757654	AAAGAATATATACAG[A/T]ATGTATAATTCCATT	54476
rs182546251	snp	C/T	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5660795	GGCTGGTCTCAAACT[C/T]CTGGAGTCAAGCAAT	54476
rs182606180	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5693547	GAGCAGGAACTAGCT[A/T]GGAAGAAGCCGGCAT	54476
rs182611363	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5648175	GCAATGGCGTGATCT[C/T]GGCTCACCATAACCT	54476
rs182679155	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5749952	ATTTAAGGAAACTTT[C/T]TTCTTTTAAGGTTAT	54476
rs182686898	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5736795	TGGGAGGTGAGCAGC[A/G]TCTCTGCCCGGCCGC	54476
rs182694442	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5724889	TATTTCATCAATAAG[A/G]ATGACAGAATTTTGG	54476
rs182695036	snp	A/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5725580	TGGCAGCTGGGTGCG[A/G]TGGCTGACGCCTGTA	54476
rs182702594	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662738	CAGATAACTGTATAC[C/T]CTGAGGAAGATGGTG	54476
rs182706583	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5645112	GAGCCACCGTGCCCC[A/G/T]CCTGTTTGCCTATTT	54476
rs182730494	snp	C/G	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5694212	TTAGGACGGCCTACT[C/G]AATTTCTTTATTTGC	54476
rs182739622	snp	A/T	0.0150606	0.0854603	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754326	TTGAACAGTTACTTA[A/T]AAAAAAAATTTTTTT	54476
rs182746923	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5777397	GAAGCAATGCAATGA[C/T]AGCTGTGCTTTAGAA	54476
rs182755613	snp	C/T	0.0287284	0.116357	intron-variant	RNF216	GRCh38.p7	7:5772173	GGGAGGTGGAGGTTG[C/T]GGTGAGCCGAGATCA	54476
rs182761811	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5728793	AGAATACAATTTAAC[A/G]GCAGTAAGAGCGACC	54476
rs182762534	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5763754	TTTTAAAATTTTTTT[A/G]TAGAGACAGGGTCTC	54476
rs182763921	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5699323	ACACCTAAAAACACA[A/T]ATAACAATGAGAAAC	54476
rs182768136	snp	A/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5769498	GAGTCTGAGGTGGGC[A/G]GACTGCTTGAGCTCA	54476
rs182880878	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5632335	AAGAAGGACCCAGCT[C/G]GCCTGAATGAGTTCT	54476
rs182881222	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5691773	GTATGAAATTGAGGT[C/G]AGAGGAAACTACACC	54476
rs182887144	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5709537	ACGGCTTTTTCTGCA[A/G]GTGATCTAACTACTC	54476
rs182903392	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753441	AAACACAAACTTTAA[C/G]AATCATTTAAGCAAA	54476
rs182903580	snp	C/T	0.00874735	0.0655527	intron-variant	RNF216	GRCh38.p7	7:5738630	GGAGAATGGCCTGAA[C/T]CTGGGAGGCGGAGCT	54476
rs182916351	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5637071	ATACTGCCTGTGGAG[A/C]TCTTCATAGCTCCAG	54476
rs182916773	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5727758	CATGATGATGATGAT[A/G]ATAATACAGACTGCT	54476
rs182919668	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5687335	TGGGAGGCGGAGGTT[A/G]CAGTGAGCTGAGACT	54476
rs182927229	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5715390	AGTATTAATCCATAC[C/T]TAAAACAGCGAGGTT	54476
rs182937578	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663445	ACAAATTAGCCAGGT[A/G]TGGTGGCGTTCGCCT	54476
rs182969936	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5778687	GAGTTCAAGTTCCAC[A/G]CTGACCCTTACAAGT	54476
rs183005151	snp	C/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5769041	CTAAATAAACTGAAA[C/G]ATAATGAAAACAAAA	54476
rs183005746	snp	G/T	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5658510	AAAAATACAAAAATA[G/T]AGCTGGCTGTGGTGG	54476
rs183016970	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5765932	CAGTCCAGCCTGAGC[A/G]ACAGAGTGAGACTCT	54476
rs183023556	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5769755	AAAAGACTGAAAATC[A/G]GCCAGGCGTGGTGAC	54476
rs183024205	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5739061	CCACTGGCTTGGGAA[A/G]GGGATGGGGAGTGAG	54476
rs183026508	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5757740	TGAGGTAAGGACTAA[C/T]TGCAAAGAGGCACAA	54476
rs183029783	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5742558	TTAAATTAGATAATA[C/T]CAAGCATTGGTGAGG	54476
rs183032568	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5683633	CTACCCCTTTGAGTG[C/T]ACACTTAACCTGGAG	54476
rs183038482	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5732134	TCCTATTACAGAGGG[C/T]GACAAGAATTCAGAG	54476
rs183049312	snp	C/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5718953	ATAAGCCACTGTGCC[C/T]GGCCAGAAACGAATA	54476
rs183051117	snp	A/G	0.0170251	0.090679	intron-variant	RNF216	GRCh38.p7	7:5715867	CTGCTTCAGCCTCCC[A/G]AGTAGTGGGGATTAC	54476
rs183069106	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5636722	CAAACGGAACAGAAT[A/C]TCCGGCTGTGGCTAT	54476
rs183073478	snp	A/T	0.000399281	0.0141238	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619878	ATCACCTGATCTTCC[A/T]CCCTGGCAGGGGAGT	54476
rs183131473	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712374	GCTACTCAGGAGGCT[A/G]AGGCATGAGAATTGC	54476
rs183182086	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663014	ATTTTGCCTAAGAAT[A/C]TCTCTTCTCCTCTGG	54476
rs183186409	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678207	GGCCCTCTGCTGACC[A/G]CCTGCTGTAACTTTT	54476
rs183192790	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5693841	AAAGACAGAGATGGA[C/T]GCGGGTAGAGACTCT	54476
rs183203236	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5651680	TTTGAGACGGAGTCT[C/T]GCTCTGTTGGCAGGC	54476
rs183220584	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5703980	CTTTTATGTAACACT[C/T]TTCAGTCTCACACCA	54476
rs183231118	snp	C/T	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5682559	ACTACAGGTGCCCAC[C/T]ACCATGCCGGGCTAT	54476
rs183244212	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5760376	ACAAAATTAGCAGGG[C/T]GTAGTGGCACATGCC	54476
rs183246324	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5746683	AAACAGCATCCCTAA[C/T]TTCTAAAAATTGGAG	54476
rs183295002	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5757212	CTTAAAAATCCCCAC[A/T]ATAATGGTGGATTTG	54476
rs183300380	snp	C/T	0.046775	0.145601	intron-variant	RNF216	GRCh38.p7	7:5653532	CGTGAACCCGGGAGG[C/T]GGAGCTTGCAGTGAG	54476
rs183301415	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5623792	CTTTAGCCAGGTGTG[C/G]CTTGATTGATTCCTG	54476
rs183301880	snp	G/T	0.00398564	0.0444627	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665461	AAGAAATCTTGAAGT[G/T]TTATTTCTGTGGATT	54476
rs183304409	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5731208	GGAAAACTGTGTGTT[C/G]ACATTTACAGTAAAA	54476
rs183310969	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682180	CTAAATTGCAAAGTT[A/G]GCAGATTCTGTACCT	54476
rs183314440	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5697904	GTCTAACAGAGCAGG[C/G]GAGAGAAGGGCAAAA	54476
rs183315336	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678707	CCTGCTACCCTCCAA[C/G]CACGCTTCCAGGAAA	54476
rs183322551	snp	C/T	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5653989	AGTTTTTTCTTTATC[C/T]TATGAGCACTAGGAA	54476
rs183356621	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5760594	CCTCAAGGCTAAGCC[A/T]GAATCTTCTGGCAAA	54476
rs183362691	snp	C/T	0.0197687	0.0974348	intron-variant	RNF216	GRCh38.p7	7:5640054	GTGAGCCACCGCGCC[C/T]GGCCAATTTTTTTTT	54476
rs183363202	snp	A/G	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5772627	TCATTAAATGTCTAC[A/G]AAGAGTTAATAGTCA	54476
rs183364900	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5623229	TTAAACCAACCTCAA[C/T]GGAATCTAGCCTGGG	54476
rs183373363	snp	C/T	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5734978	CAACATGGTGAAACC[C/T]TATCTCTACTAAAAA	54476
rs183453972	snp	C/T	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5637634	TCACTGCATCCCTAA[C/T]GTCCCGGGCTAAAGC	54476
rs183457364	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5644272	AACTGTTAACTATGG[C/T]GGCTACACTATTTCT	54476
rs183476657	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5698494	TTCTGGGCTCAGGTG[A/C]TCTTCCCGCCTCAGC	54476
rs183511254	snp	A/C	0.0178098	0.0926698	intron-variant	RNF216	GRCh38.p7	7:5723570	GAGAATGGCGTGAAC[A/C]CAGGAGGCGGAGTTT	54476
rs183529755	snp	A/G	0.0142736	0.0832652	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620606	GACCCTCCAAGGAAA[A/G]AGGCCGCCGCTCCTT	54476
rs183537879	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5725210	CAGTCACTCCTTGGA[C/T]TGGCCTGTCCAGATG	54476
rs183553599	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5640276	TATTATTTTTTAGTC[C/T]GGCCTTGATGTAATG	54476
rs183568983	snp	A/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666598	ATGAGGTTGATTCCC[A/T]AAGAACCCCACCTGC	54476
rs183588930	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5773786	TTGGCCAGGCTGATC[A/T]TGAACTCCTGACTTC	54476
rs183594272	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5747425	ATATTCAGGACCTGA[C/T]AAGTACTATCCAGTC	54476
rs183612380	snp	A/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5777062	GGTAAAAAGTCTGAA[A/T]ACCCTGCTGAGAGAT	54476
rs183626571	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5749561	AATAACTAAATTTCC[C/T]TGTCAACTGTGTCAT	54476
rs183647724	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672080	AAGGAGTAGATGGCA[C/G]TGGATCAGAGAAGTT	54476
rs183693871	snp	A/C	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5777513	AGAAGAATACAAGAC[A/C]CTGACTGCAGAGTTA	54476
rs183697451	snp	A/G	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5627654	CGGGAGGCTGAGGCA[A/G]GAGAATGGCTTGAAC	54476
rs183704533	snp	A/C	0.00557542	0.0525036	intron-variant	RNF216	GRCh38.p7	7:5744059	AAGAGAAGTAACAGA[A/C]AACAGAAACAAATAT	54476
rs183709263	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5732373	AAATGGTCTGTTTTT[A/G]CGTGTTTTCTCAAGT	54476
rs183715705	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5721351	CATTAGCCAACCTAC[C/T]ATCCATTTTTTGACC	54476
rs183745860	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5689392	AAAGAAAGAAGAAGA[A/G]AAGTGAAAGGCAAAA	54476
rs183751075	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5706668	TACTGTGAATAATGC[G/T]GCAATGAACACAGGA	54476
rs183773181	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5758406	TTTGACCTAATAAAA[C/T]TTGCTCAATTTTAAA	54476
rs183774371	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5771049	TTGACCTTGTGATTC[A/G]CCCACCTTGGCCTCC	54476
rs183792100	snp	C/T	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5632959	AAACGGGAGTCTCAC[C/T]CACCCAGCGGAACTG	54476
rs183805352	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5659550	GGAGTTTGGAAAGCT[A/C]GGCTGACCAGGTGGG	54476
rs183813959	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5691231	ATGGTGAAGGGGAGA[C/G]AAGCCACCTGACACC	54476
rs183827722	snp	G/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5763308	TATACTAAAATGGAT[G/T]GATTTTATTTTAATT	54476
rs183852786	snp	C/T	0.0418186	0.138422	intron-variant	RNF216	GRCh38.p7	7:5736594	CCATCGTCTGGGATA[C/T]GAGGAGCCCCTCTGC	54476
rs183892035	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5692264	GGATTTGCCACTAAG[C/T]CTTTTACTTGTTCCT	54476
rs183894228	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668530	GCCAGGCCACAAAGC[A/G]GACTTTTAATCTTTC	54476
rs183897450	snp	A/C	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5710033	TGCTGGGATTACAGG[A/C]ATGAGCCACTGGGCA	54476
rs183901787	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5686095	AGGCGTGGTGATGCA[C/T]GTCTGTAATCCCAGC	54476
rs183921165	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5723219	CATATTAAGTGCTCA[A/C]TGTTAATTACTGTAA	54476
rs183931447	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5748041	TGCTCCAAGAAAAAT[C/G]AAACTGTTGCTAAGC	54476
rs183941967	snp	G/T	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5735122	CTGCACTCCAGCCTG[G/T]GCAAGAGAGTGAGAC	54476
rs183953842	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5723673	ATAAATAAATAAATG[C/T]AATTAAGTCTACAAA	54476
rs183977908	snp	C/T	0.0463947	0.145069	intron-variant	RNF216	GRCh38.p7	7:5648521	ATGAGGTCAGGAGAT[C/T]GAGACCATCCTGGTT	54476
rs184001976	snp	A/T	0.00199481	0.0315187	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673700	GAGCAACACAGCATG[A/T]CCTTGTCTCTACAAA	54476
rs184012041	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5774433	GGCAGAGGGAGAACC[C/T]ACCTCCAAAAAAATT	54476
rs184012354	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5761194	ATCAAAACTCTTGCC[A/G]TGTATCTGGTCAGGG	54476
rs184031984	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5765271	GTTGAGACCAGCCTG[A/G]GCAACACAGTGAGGA	54476
rs184054213	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5751200	CAACAACAACAAAAA[A/G]AAGTGTGATAATGAG	54476
rs184054994	snp	C/T	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5737820	CCAGGCTGAGCACGG[C/T]GGCTTATGGCTGTAA	54476
rs184063882	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5726623	AGCACTTTGGGAGGC[C/T]GAGGCAGGTGGATCA	54476
rs184070354	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713876	TATTTCCATTTTACA[C/G]AGGAAGAAACAGTGG	54476
rs184106369	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5708256	TGTCTGTTAGGTCTA[C/T]AGTGTTGTTCAAGTC	54476
rs184113314	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5629947	GTGACAGATGGGGTA[C/T]TGAGTCCATTCTGGA	54476
rs184114129	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5777979	ATCAACGTTTTCAAC[A/C/G]ATCTTTTTAGAACTG	54476
rs184114454	snp	A/C/G	0.0158469	0.0875917	intron-variant	RNF216	GRCh38.p7	7:5779889	GCAGAGAGGAGCTGA[A/C/G]GGGACATACTACATC	54476
rs184123952	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5631027	GCAACTGTTCTAAGG[C/T]GTGCTTTATTCTATA	54476
rs184145584	snp	A/G	0	0	intron-variant	RNF216	GRCh38.p7	7:5657180	CTCACTCTCTAGGGG[A/G]AGAGAAGTCACTGAC	54476
rs184226936	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5646509	CTATCCTGGCTAACA[C/T]GGTGAAACCCCATCT	54476
rs184232851	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5656793	TTAATGAATAAAGCA[A/G]AAGATTAAATTCAAT	54476
rs184233391	snp	A/G	0.00557542	0.0525036	intron-variant	RNF216	GRCh38.p7	7:5763917	CAGACGGCAGGGCAC[A/G]ACAGCTCATGGCTGT	54476
rs184236374	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671480	TGAGGCTGATGGGGT[A/G]AGCGCTATTCCAATC	54476
rs184246564	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5689086	CTGTGAAACAAAATG[A/G]TATCCTATTATATGG	54476
rs184255089	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5754951	GAGAATCGCTTTAAC[C/T]TGGGAGATGGAGGCT	54476
rs184256035	snp	C/T	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5737037	GTTCCCAACAGCTTA[C/T]TGAGAACGGGCCATG	54476
rs184257711	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767352	TGAGGCAGAAGCAGC[A/G]ATTTCAATGGGCTGA	54476
rs184270471	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5739813	CAAAACCAGCCTGGC[C/T]AACATGGTGAAACCC	54476
rs184270695	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663565	CTCCAGTCTGGGCGA[C/T]ACAGCGAGACTCCAC	54476
rs184273922	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5646978	GTTGAGCCCTAGACA[C/T]GTACGTAGTCTTCTA	54476
rs184276381	snp	A/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5730166	AATGACCTGCATGCT[A/G]AAGTACTTAGAGGGA	54476
rs184287062	snp	A/C	0.00597247	0.0543191	intron-variant	RNF216	GRCh38.p7	7:5695144	GAAGTTAGCACTTAA[A/C]CTATCCACGGTTCTT	54476
rs184296400	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713453	AAATGGAGTCTGCAT[A/G]ATGAACAGAGAACTC	54476
rs184324316	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5780224	CTTCCTCACAAGGGA[A/G]GAAACCCCATTTTTG	54476
rs184349252	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5648827	TAGAAGACATTCTAC[A/G]GGCCAATTATCAAAT	54476
rs184353970	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5660079	CCCGCCTCTATCTTC[C/T]GAGTAGCTCGGACTA	54476
rs184365649	snp	A/C			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674343	TTCAAATTTTTAGTA[A/C]AGATGGGATTTCACC	54476
rs184389150	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5750408	AAATATGTGGTTAGT[A/C]AGGCAAACTGGTCTT	54476
rs184415780	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5726067	GGATCACTTGAGCTT[A/G]GGTGTTCAAGGCTTG	54476
rs184422665	snp	A/C			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664305	CTTTCAGGTTAATTC[A/C]TTACAGCTTCAGCCT	54476
rs184428129	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5633370	CATTTGAGGTCAGGA[G/T]TTTGAGACCAGTCTG	54476
rs184432431	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680487	GCTCACTGCAATCTC[C/T]ACCTCCCGGGTTCAA	54476
rs184442754	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5695778	CAAACTGTTCCCTTA[C/T]GTGTTCTTCCCTTGC	54476
rs184450835	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674938	GGAGGTGGAGGTTGC[A/G]GTGAGCTGAGATCGC	54476
rs184474832	snp	A/C/T			intron-variant	RNF216	GRCh38.p7	7:5726326	GTACAGGTAAAATCA[A/C/T]ATGACAATGGGCTGG	54476
rs184483995	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713586	CATTCAGGTTCATAA[C/T]ATAAAAGCTAACTGG	54476
rs184485277	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5701832	GTAAGGGCTTCAAAA[G/T]AACTGTTGAAACAGA	54476
rs184494201	snp	C/T	0.00795532	0.062565	intron-variant	RNF216	GRCh38.p7	7:5638620	CAGATTGTGGCCAGG[C/T]AGAAAAGCAAGCATT	54476
rs184514272	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652234	CTTCTGAAATAACTC[C/T]ATGAGGCTGCAGAGA	54476
rs184534977	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5649341	AGGTCGCAATGACCC[A/G]AGGCACTCTAACCTA	54476
rs184570022	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780620	TGAGGCAGGAAAATC[A/G]CTTGAATCCGGGAGG	54476
rs184585415	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5755173	AGAAAGGAAGGAAAG[A/T]GAGGAAAGGAAGAAG	54476
rs184594945	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5730352	CGTAAAATATTTCAA[C/T]TTTTCTGTAGGTTTG	54476
rs184641140	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5717560	GGAATGATGTATGCA[C/G]AAACTTATCATGGCA	54476
rs184650858	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5634219	TGGGGGAAGAACGGG[C/T]GGCTTTTCTTCTTCA	54476
rs184654980	snp	A/C	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5654140	AAAGCCACTCAGGAG[A/C]GAGGCCATGAAGGCC	54476
rs184669995	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5660458	GACCACACCTGGCTA[A/G]TTTTTCTATTTTTAG	54476
rs184699168	snp	G/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767587	AATCTCAGCAAACAT[G/T]TATTGTTGAGAGGGA	54476
rs184712191	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5739651	GGAATCCAAACACAA[A/G]TAAGTTACAATCTCA	54476
rs184716240	snp	C/T	0.00874735	0.0655527	intron-variant	RNF216	GRCh38.p7	7:5728843	CTCTGCTGGTGCGTG[C/T]GCTCCTGTTCTGGCC	54476
rs184723516	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5740346	TTAGCCAGGATGGTC[C/T]TGATATCCTGATCTT	54476
rs184726431	snp	C/T	1.64838e-05	0.00287083	missense	RNF216	GRCh38.p7	7:5716737	ATACTGTTCTTCATT[C/T]ATCTGTAGGGCAAGC	54476
rs184753977	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667496	TAAGGAACAATGCCC[A/G]GGAACCAGGGGAACC	54476
rs184760320	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5634741	TTTGCGTCCCGTCAG[A/G]GTCAAGTGCTCACCC	54476
rs184761606	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5684019	AAGACCAAGGCAGCA[G/T]CAAGTTGATTTGGTC	54476
rs184764530	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5649513	GACACTGTCTCAAGG[C/T]GAGAAAAAAAACGTT	54476
rs184768034	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5700177	CCTGGAAGGCTGGAA[A/G]CCCTGCAGTGCTCTG	54476
rs184775686	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5720327	CTTCTCATGCTGATC[C/T]ACACTTCCATTTAAT	54476
rs184812314	snp	C/G	0.00159617	0.0282053	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620262	TAAGTGCAAATACTA[C/G]ATTCCTCTCTCCAGT	54476
rs184838463	snp	C/G	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5770211	TCACATCTGTAACCC[C/G]AGCACTTTCGGAGGC	54476
rs184867315	snp	C/T	0.0146672	0.084371	intron-variant	RNF216	GRCh38.p7	7:5743037	GGAGGCCAAGGCAGG[C/T]GGATCACGAGGTCAG	54476
rs184961666	snp	A/G	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5758061	GAAAAAAGTTCTCAT[A/G]ATGGGTGCAGAGTAT	54476
rs184965358	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5774994	AGGTGATCCACCCCC[C/T]CGACACTCACCAAAG	54476
rs184969748	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5706268	ACACAATACAAAAAC[C/T]ACCCAATTAACACAT	54476
rs184974571	snp	A/G	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5761711	GAATCGCTTGAACCC[A/G]GGAGGCTGAAGTTGC	54476
rs184979110	snp	C/T	0.00557542	0.0525036	intron-variant	RNF216	GRCh38.p7	7:5625605	AGAAATGAGTGATTT[C/T]CCCACACAATTGTTT	54476
rs184984462	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5732202	TCTCCATCCTAGAAT[C/T]CACTGGTGTGCACTG	54476
rs184985887	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5707441	TGGAGTGTTTGTTAG[C/T]GTACAGGAACGCAAC	54476
rs185001894	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5654924	GAAACAAACCCTGTG[C/G]CTGACTATTGCAGGA	54476
rs185019198	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5685010	CACAGCATAGGTGGA[A/G]GGGTGAAGAGAGTGC	54476
rs185038887	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5772455	TGTGTCACCCAGGCT[A/G]GAGTGCAGTGGTGCG	54476
rs185039018	snp	C/T	0.0158469	0.0875917	intron-variant	RNF216	GRCh38.p7	7:5759885	ATCCACCCGCCTCGG[C/T]CTCCCAAAGTGCTGG	54476
rs185052828	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5746381	ACGGCTTGAGTCAAG[A/C]CCCCAAGATTATGGC	54476
rs185054398	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5734323	TAAACTTAACATAAT[C/G]CTGAGTGAAAAGAAA	54476
rs185065613	snp	C/T	0.00953873	0.0683987	intron-variant	RNF216	GRCh38.p7	7:5723110	GTGCTTCACTTTTTT[C/T]CTATAAAATGATAAT	54476
rs185108132	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5717278	AGATTACTTGAACCT[C/G]GGAGGCAGAGGTTGC	54476
rs185115268	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668046	AATTCATGTATCCAG[C/G]GACAGAAGAATACAA	54476
rs185141832	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622782	GCAATGGTACAGACA[C/T]CAGCCTTGGGGGAGG	54476
rs185153628	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5639860	TGCCTCCTGGGTTCA[C/T]GCCATTCTCCTGCCT	54476
rs185163187	snp	A/C	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5762482	CCAACACGGTGAAAC[A/C]CCATCTCTACTAAAA	54476
rs185237749	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5701085	GGACAGAGAGTGCAG[A/G]CCCTGAGAGTGGGAG	54476
rs185264370	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5683812	GATAAAACCTGTTAA[A/C]AGTGCAAGATAAGCC	54476
rs185267597	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5653020	TGCTTGGCAGGGCCT[G/T]TTTGGATCTCGTTAA	54476
rs185270735	snp	A/G	0.00557542	0.0525036	intron-variant	RNF216	GRCh38.p7	7:5776312	ACTATAGCCGGGCAC[A/G]GTGGCTCAAGCCTGT	54476
rs185274823	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5706036	TCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT	54476
rs185280386	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5762869	AGCAAACAAGACAAA[A/T]CATGAACATATGTTA	54476
rs185280714	snp	C/G	0.00636936	0.0560724	intron-variant	RNF216	GRCh38.p7	7:5748769	TTGGTCAACAGTATG[C/G]TATTAGTACTTAAGT	54476
rs185280948	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665110	GCCAGGACACACAAA[A/G]TTCTAACATGAATTC	54476
rs185298291	snp	C/T	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5736388	CGGCCTCCCGAGGTG[C/T]CGGGATTGCAGATGG	54476
rs185302663	snp	A/C	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5724635	GAGCCTGAAAAGTTC[A/C]TAGTAAATACAAATA	54476
rs185312098	snp	A/G	0.00398564	0.0444627	intron-variant, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711397	AAAAGGTGTGTGTGT[A/G]GGGAGGGAGGGGTAG	54476
rs185350352	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621428	AGTGCTGGGATTACA[A/G]GCGGGAGCCACCGCG	54476
rs185359116	snp	C/T	0.0287284	0.116357	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670984	TGAACTGCTTGGTTC[C/T]GGGGGAGCTGCCGGA	54476
rs185360479	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5776550	CAGTGAGCTAAGATC[A/G]GGCCACTGCACTCTA	54476
rs185396813	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5777853	AAAATCTTCAGTGGG[A/C]GGGCTAAACAATTTA	54476
rs185411542	snp	A/G	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5750880	CCAGTCATGGGATGC[A/G]AGATTACCTACTAAC	54476
rs185421834	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5655125	TCATAAGGGAAGAAA[C/T]CCCATTTTTGAGATG	54476
rs185438598	snp	C/G	0.0189856	0.0955633	intron-variant	RNF216	GRCh38.p7	7:5737407	CCCAGGGTCCTCTGC[C/G]TAGGAAAACCAGAGA	54476
rs185444355	snp	C/T	0.0146672	0.084371	intron-variant	RNF216	GRCh38.p7	7:5629670	CATCTCTACTAAAAA[C/T]ACAAAAATTAGCTAG	54476
rs185465849	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656507	GACTGGGGGAAACCA[C/T]GGAGTTCACCGTCAT	54476
rs185472091	snp	C/G	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5719895	AGACAAGCTTCATAT[C/G]CTGGGATGTGGCAGA	54476
rs185481326	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672840	GGAGCTGGGGCTTTC[C/T]AGGACACAGGGACAC	54476
rs185486268	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5688678	TTTACACATCTGACA[C/G]TGTATCTTCTGGAGA	54476
rs185487190	snp	A/C	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5690103	GGAGGCTTAGGCGGG[A/C]GGATCACCTGAGGTC	54476
rs185493127	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5707273	TATGCATTTTAGGGA[C/T]GTCTTTCCATTTATT	54476
rs185499957	snp	A/G	0.00557542	0.0525036	intron-variant	RNF216	GRCh38.p7	7:5642829	AAAAGCTATGTGCCC[A/G]AACACAACTGCAATT	54476
rs185502595	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5626357	TCAACTCTCTAGACT[A/G]GGAGCTGGCAAGCCT	54476
rs185503688	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5641773	AGCATGGTGGTGCAC[A/G]CCTGTAATCCCAGAA	54476
rs185521385	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5764563	TGAGGCGAGAGAATC[A/G]CTTGAACCCGGGAGG	54476
rs185547044	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5632122	TGCTGGGCTCACCCT[C/G]GACAGCGGTCTATAG	54476
rs185563104	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5647889	CCTTCTAAATTTTCT[A/C]CTTTATTCAAGTCTT	54476
rs185567881	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5657745	CCCCACCCATACGCC[C/G]AAATGACATACAGAA	54476
rs185622900	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5624598	TCCAGTCGGGCCCTG[C/T]TTAGCCCCCAAGGCT	54476
rs185626671	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5660863	ATGTGAGCCACCATG[C/G]CTGGCCTGGGGAACA	54476
rs185631222	snp	A/G	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5748394	AATTCCAAGTAGCTG[A/G]GATTATAGGTGCTCA	54476
rs185639776	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5766286	CAGAGTGAGACACTG[C/T]CTCAAAAAACTAAAA	54476
rs185641701	snp	C/T	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5692534	TCACTGGCTGTATCC[C/T]GTCCGACAGTGCCAG	54476
rs185706934	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5650534	GCTGCTCATTTGGGT[A/G/T]GTCTGCAGAATTCAG	54476
rs185712687	snp	A/T	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5627987	TCTGAGGCACCTGCA[A/T]AGGAGCGCGAGCCCA	54476
rs185766342	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675201	AACAGTCTGTTGTAT[C/G]CTAGTTACTATGCTG	54476
rs185772888	snp	G/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5735362	GGGAGCCAGCAGGAA[G/T]AACAGAATATGATTC	54476
rs185776721	snp	A/G	0.0107246	0.0724382	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754494	TAAGGATGAGGAGTT[A/G]CCAAGCTCCTCACTT	54476
rs185782238	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5724234	CAGGGAAGAGGAGAA[A/G]GGCAGTCAGGCTGAT	54476
rs185784783	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5710409	CCTCAGAGAATAATG[A/G]TCTCTCCTCTTCTTT	54476
rs185798410	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5778707	CCCTTACAAGTTTTG[C/G]GACTAGATATTTTTC	54476
rs185820915	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5661502	GGAGAATTATTCCCA[A/T]TTTTAAAAAAGTAAA	54476
rs185829117	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677070	AGAAATACCACTACA[G/T]ACCACATACATCTCC	54476
rs185835058	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5692797	TTAATACAAACAAAA[C/G]AAAAATTCTTTTGCT	54476
rs185845343	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5710850	AGCACACAAGGGACA[C/T]GCTAGCACTCTGCTT	54476
rs185864323	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5714373	AACCAATTCTCCTGC[C/T]TCAGCCTCCCCAGTA	54476
rs185929167	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681899	ACGGGATCTGTGTAG[C/T]CCCTAAGGGTGGTAA	54476
rs185934773	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5765404	GGAAGGTGGAGGTTG[C/T]AGTGAGCTGAGATTG	54476
rs185945335	snp	C/T	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5738337	CTCAGGCAATCCTCT[C/T]GCCTCAGCCTCCCAA	54476
rs185969513	snp	A/C/T	0.00239393	0.0345281	intron-variant	RNF216	GRCh38.p7	7:5631928	GCTTAGCTCACACCC[A/C/T]CTTCTCCACGCCACG	54476
rs186055111	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782142	GGATCACTTGAGGTC[A/G]GACGTTGGAGACCAG	54476
rs186057603	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5778484	AAACTATGTGTAATT[C/T]TGGTCTCCTCTGCTA	54476
rs186063677	snp	C/T	0.0146672	0.084371	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768889	GATGGTCTTGATCTC[C/T]TGACCTCGTGATCCA	54476
rs186063931	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5697728	TTGAGGTGCTTAGGA[G/T]GCAAGGGTGCTCGCC	54476
rs186065395	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5756912	AAGTGCTGGCATTAC[A/G]AGCATGAGCCACTGC	54476
rs186070592	snp	C/T	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5752003	CCAGCCTGGCCAAGA[C/T]AGTTAAACCTATCTC	54476
rs186071688	snp	A/G	1.64735e-05	0.00286993	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741148	GGATGGGCAGGCTGA[A/G]GAGAAGAGGGGCCTG	54476
rs186075477	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5650875	TAATGGTACCCACCT[C/G]TGCTGCATACTTGGG	54476
rs186091431	snp	C/T	0.00636936	0.0560724	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677689	GTAGGTGAATCCCCT[C/T]CCAGTCCTGGCCTGA	54476
rs186203516	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5635947	CAAACTCTTACATTC[A/G]AAAGACAAAGACACT	54476
rs186211643	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662719	CTTAGAGTCTACTCA[C/G]AAACAGATAACTGTA	54476
rs186220072	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782708	TACAAAAATTAGCTG[A/G]GCATGGTGGTGCGTG	54476
rs186223055	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5653705	TACAGTGAAGGAAAA[C/T]ATAGTGTTGTCAGTT	54476
rs186231444	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665590	AGTTACAAGGCACCG[A/T]GACACCAGCTTGACT	54476
rs186234135	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5693159	CCAATCTGGCCCTCT[A/G]CCAATTTTTGTAAAT	54476
rs186241070	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5757627	TTACCTTTCACAAAA[G/T]AATTCCAGTACAAAG	54476
rs186285620	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753044	CCAACTCTTTAAGTT[A/T]TTCCTGACAGGGGTA	54476
rs186287902	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5771512	GAAAAGAAAAAGAAT[A/C]CCGGCGGGGTGCAGT	54476
rs186292799	snp	A/C	0.0275645	0.114116	intron-variant	RNF216	GRCh38.p7	7:5738448	GAGCGGTGGCTCACA[A/C]CTGTAATCCCAGCAC	54476
rs186295600	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5727505	GTGGAGGTGGGAGGA[C/T]AGCCTGAGGCCAGGA	54476
rs186296336	snp	C/G/T	0.00119752	0.0244452	intron-variant	RNF216	GRCh38.p7	7:5758822	GATAAGACTGGACTT[C/G/T]TGAGTTAATGCTAGA	54476
rs186298636	snp	C/G	0.000148257	0.00860851	missense, intron-variant	RNF216	GRCh38.p7	7:5741680	ATGGGTTGTTACACA[C/G]TGAAAAATAGCTGCT	54476
rs186299931	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5714865	GAAGAATTCTACTGT[C/G]CCCTGAAAAGAAATC	54476
rs186315611	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682340	CAGCCATGGAGCACA[C/T]GTTACTACTTAGCTT	54476
rs186322336	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5697947	GTCAAAGATAAGAGC[A/G]GAAGAAATTGTGATC	54476
rs186348016	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5697285	TCACCATCACTCTCT[C/T]ATCCCACTGATGGTC	54476
rs186384258	snp	C/T	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5776852	GTTGCAGTGAGCTGA[C/T]ATTGTGCCACTGCAC	54476
rs186390266	snp	C/T	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5769238	TTCTCCTGCCTCAGC[C/T]TCCCGAGTAGCTGGG	54476
rs186408411	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5722919	GCAGGAGAATCGCTT[C/G]AGCTTGGGAAGTGGA	54476
rs186441468	snp	A/C	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5639391	TACACATAGAGGAGA[A/C]ACACACTTCTGTTTT	54476
rs186442307	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5651188	TCATGCAGAAGAGAA[C/T]ATCACCTTCAGGGAA	54476
rs186443697	snp	C/G	0.00795532	0.062565	intron-variant	RNF216	GRCh38.p7	7:5686378	ACAACCACCCTGAAG[C/G]GGGCTGGGACAGAAA	54476
rs186444906	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662741	ATAACTGTATACTCT[C/G]AGGAAGATGGTGAGT	54476
rs186460948	snp	C/T	0.00398564	0.0444627	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664699	CCCAAGGGTAGGCTG[C/T]ACGCTTCCCCCACTG	54476
rs186478425	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5756199	CTGCCTCCTGAGAAG[C/G]TGCCTGCTTCTCCTT	54476
rs186482880	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5740623	CTAGTAAGTGCCATA[C/T]TGGACAGCATAGGTC	54476
rs186493287	snp	C/T	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5730563	GATCGCACTGAAGTA[C/T]AGATATATTCTGAAA	54476
rs186495670	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5771698	GCTACTCAGGAGGCT[A/G]AGGTGGGAAGATCTC	54476
rs186499377	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5718071	AACCAAAGACTAACA[A/G]TAATGGTTATATATA	54476
rs186501061	snp	A/G	0.0162398	0.0886349	intron-variant	RNF216	GRCh38.p7	7:5745509	AAGCATAAAAATTGG[A/G]AAGACAGATCAGATG	54476
rs186515627	snp	A/C	0.00755907	0.0610114	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668850	CGGTGTATCTTCCCC[A/C]TATCTTTACTACGGG	54476
rs186576751	snp	A/C	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667051	GGCTCAAAGGATGCA[A/C]CCGCCTCGGCCTCCC	54476
rs186578700	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5683819	CCTGTTAAAAGTGCA[A/C]GATAAGCCCAGCAGA	54476
rs186611672	snp	A/C			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622062	GCAGAAACGTCTCCC[A/C]CAGCAGTTGGGCTGC	54476
rs186617210	snp	A/C	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5733737	GGAAATACAATTAGT[A/C]AACAAATATTTGAAA	54476
rs186625174	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5652707	GGGCTAGGTGGCTGA[C/T]GCCTGTAGTACCAGC	54476
rs186635187	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5640995	ATGAGGAGTAGCTGA[C/T]AATTAGTTTCTCAAA	54476
rs186636754	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5624497	TGAAAAGTTTCAGAT[C/T]CCAAGTCCACAAGCG	54476
rs186646712	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5690911	GGAATTGCGATTTGG[G/T]GGCTGAAGACAACCT	54476
rs186650349	snp	A/C	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5654134	GCTAGTAAAGCCACT[A/C]AGGAGAGAGGCCATG	54476
rs186651436	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5735912	CCAGCCTGGCCAACA[A/C/T]AGGGAAACTGTCTCT	54476
rs186655582	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680968	TGGCTGGGCCATGGC[A/G]GAGAGCCTGGACTTC	54476
rs186709497	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5759065	CACAATCCGTTCTGG[G/T]TGCAACAGTGAGTTC	54476
rs186716920	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656135	TTAGCCGGGCATGGT[A/G]GCGGGCTTCTGTAAT	54476
rs186738534	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5687084	TATAGAAACACCAGG[A/T]TCAAAATCAAAATCT	54476
rs186755206	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5718284	TACTAAGGTGGCTGA[A/G]GCAGGAGAAGCCCTT	54476
rs186772612	snp	C/T	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5628107	GGGAGCCTCAGAGTC[C/T]CAAGGGAATAAAAGT	54476
rs186779411	snp	A/G	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5645027	TCATCATATTGGCCA[A/G]GGTCATCTCGAACTC	54476
rs186783441	snp	A/G	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5656215	TGGAGGTTGCATTGA[A/G]CTGAGATGGTGCCAC	54476
rs186799896	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5774551	GTGACATTGTGCTAT[G/T]TTTATTAACTGTTAC	54476
rs186872466	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669877	AGCCTGGGCAAGACT[C/T]CATCTCAAAAAAAAA	54476
rs186880126	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5647289	AACAATGCAGCTGAC[A/T]TGCCATGTCCACATC	54476
rs186884260	snp	C/T	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5687524	GATACTGTAGAAAGA[C/T]TCTCATATTGGCACT	54476
rs186890335	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5704239	GTTTATATTAATGCC[A/G]TATTAATATAAACGC	54476
rs186901630	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5623392	TGGCACCTTGGAAGG[C/T]GGCACGTCCACCCAC	54476
rs186908724	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672596	AACACATGTTGAATT[A/G]CATTTTTATCCACTT	54476
rs186917007	snp	A/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5644312	TCAATGTATACTGGT[A/G]TCATTTTTTCTATAT	54476
rs186923395	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5706899	GTTTTTATAGTTTCA[G/T]GTCTTACACTTAAGT	54476
rs186956536	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5731066	GCAAACTCCTCTGAA[A/G]TTTATGTATCAATTG	54476
rs186960775	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5703049	AGGGACCCATGCTGG[A/G]CTCTGAAGAAAGTGA	54476
rs186966932	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5748528	ATTATAGGCGTGAGC[C/T]ACCGTGTCCAGTTTC	54476
rs187009937	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5733036	GTTCCATCTGAAGGC[C/G]ATTTAAAGATGCACA	54476
rs187032920	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5777447	GTGTAAGATGGCATG[C/T]AGGAGACAACCGGTG	54476
rs187041605	snp	A/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5763791	CTGCCCAGGCTGGTT[A/T]GGATATCCCGGTCTC	54476
rs187058349	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750376	TTCCAGCAAAGCAAA[C/T]TTAAATATGTGCTTT	54476
rs187062834	snp	C/T	0.0107246	0.0724382	intron-variant	RNF216	GRCh38.p7	7:5736813	TCTGCCCGGCCGCCC[C/T]GTCTGAGAAGTGAGG	54476
rs187065149	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5778562	AGCCCCAGGACATAG[C/T]ATATCGGATGGCACA	54476
rs187069834	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5725660	TTCGACACCAGTCTG[A/G]CCAACATGGTGAAAC	54476
rs187096786	snp	A/G	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5657508	GGAGGTAGTGGTTGC[A/G]GTGAGCCGAAATCTT	54476
rs187105035	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5640077	TTTTTTTTTTTTTTT[A/T]AATGAGATGGGGGTC	54476
rs187187747	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5633848	AGGTAGAATTTACCA[A/G]AGAGGTTTTAATTAA	54476
rs187197235	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5649069	TTGCTTGAAAACACT[A/G]TAGCAGTTTAAAAAC	54476
rs187209863	snp	C/G	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5693687	GGAAATTCCCCTTTG[C/G]TATATCAAAGCTGCT	54476
rs187211987	snp	A/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5744690	ATAAAGAAAACTTCT[A/G]GCTAGGCACGGTTGG	54476
rs187223269	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674660	AATGAAAAAAGTCAG[C/G]TGGGAATTCCTGGGG	54476
rs187234169	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5725142	GGAAGAAGGAAGCCA[A/G]CAAGTGCAGCCACTT	54476
rs187269866	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5765720	GGCTGAGGCGGGCAG[A/G]CTGCCTGAGCTCAGG	54476
rs187281853	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5765861	CTCAGGAGGCTGAGG[C/T]AGAATTGCTTGAACC	54476
rs187283285	snp	C/G	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5735038	GTAATCCAAGCTACT[C/G]AGGAGGCTGAGGCAG	54476
rs187285569	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754193	CAGGGTCTTGCTCTA[C/T]TGCCCAGACTGCAGT	54476
rs187291077	snp	A/G	0.0295035	0.117819	intron-variant	RNF216	GRCh38.p7	7:5723576	GGCGTGAACCCAGGA[A/G]GCGGAGTTTGCAGTG	54476
rs187300475	snp	A/G	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5643326	AAGTGAAAAATGGGG[A/G]AAAATCATGGTTGAT	54476
rs187302398	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5738790	TTGTTACAATCGTAG[C/G]GAAGAAAATGTCTTA	54476
rs187307213	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5728129	TAGTTCTCACCCCAA[C/T]AAATGATACTAACAT	54476
rs187313970	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5691883	TACCTTCCCACTTAA[G/T]GCTTTTACAGCGGAA	54476
rs187321602	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5709858	CTCCTGGGCTCAACT[C/G]ATTGTCCTGCCTCAG	54476
rs187353134	snp	C/G	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5749047	TTTATCAGAAAAACA[C/G]GACCTAACTCCAATG	54476
rs187364602	snp	A/C	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768612	ATGTTCTCTGACAAC[A/C]GTCAATAAAAGATAA	54476
rs187394114	snp	A/C/G	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5770073	GAAAATCGGCTGGGC[A/C/G]TGGTGGCTCACGCCT	54476
rs187403490	snp	C/T	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5757910	CTGTAATCCTAGCAC[C/T]TCGTGAGGCAGAGGC	54476
rs187414131	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677956	CCACACTCTTAACTG[C/G]AGCAGTAAGACCACA	54476
rs187443994	snp	A/G	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5693968	GTTGTTGACCAAAAA[A/G]ACAAAGGCTTCCAAC	54476
rs187445671	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5731430	AGACTCTCTTCACAC[A/C]AAACCCACTAGCTTT	54476
rs187466447	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF216, MIR6874	GRCh38.p7	7:5711861	TCAGAACAGCAGAAC[C/T]GACATTACTTCAAAC	54476
rs187466601	snp	C/G/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5627542	CACGAGGTCAGGAGA[C/G/T]AGAGATCATCCTGGC	54476
rs187491012	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736684	AGTGAGGAGCGTCTC[C/T]GCCGGGCCACCCATC	54476
rs187497437	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5725508	GAGACAGGCAATCCC[C/T]GAATGCCATTTTAAC	54476
rs187504278	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712403	GCTTGAACTCAGGAG[A/G]CGGAGGTTGTAGTGA	54476
rs187506505	snp	C/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5655521	TGAGGCAGGAGAATT[C/G]CTTGAACCTGGGGGG	54476
rs187507399	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5651562	AATAACGTCAGGAGA[C/T]AGATATGCACCCTCA	54476
rs187507684	snp	A/C	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663078	CAGTGGCTTGGGAAA[A/C]CCAAATGACCCGGGA	54476
rs187513660	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5646226	TTTTGTAAATTAGCC[A/G]GGCATGGTGGTGCAT	54476
rs187513841	snp	A/G	0.00597247	0.0543191	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678286	TTTACTGCCATCTAC[A/G]AGACTTTCAATTATG	54476
rs187539761	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5700245	CCTCAGCACACACCA[C/G]AAGCCGCACACGTGC	54476
rs187557201	snp	C/T	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5739189	ACCAAATTGTATATT[C/T]AAAAATGATTAAAAT	54476
rs187561686	snp	A/C	0.00835141	0.0640778	intron-variant	RNF216	GRCh38.p7	7:5632579	GTCAGGGGTTCGAGA[A/C]CAGCCTGGCCAACAT	54476
rs187572512	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5716328	CAGCCTGGCCAACAT[A/G]GTGAAACCCCGTCTC	54476
rs187576866	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5658923	AGGCCTGGAGAGTGC[A/G]GCAATGTGTCGGAGT	54476
rs187584566	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767114	ATGACAAAGTATTAA[C/T]AGCCTATAGTAGACC	54476
rs187607463	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5763128	GACAAAAAAAACAAC[A/C]ACCCATGTCTATTAT	54476
rs187607612	snp	A/G	0.00318978	0.0398085	utr-variant-5-prime, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781675	CCGCGGCGTCACCTC[A/G]CGCCTGCGCACAGCG	54476
rs187614804	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5772666	CAGCATTTTCTCAAC[C/T]TATAGAATGTGAAGT	54476
rs187616181	snp	C/G	0.0107246	0.0724382	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754495	AAGGATGAGGAGTTG[C/G]CAAGCTCCTCACTTA	54476
rs187620705	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5739757	TATAATCGAAGCACT[C/T]TGGGAGGTCGAGGCA	54476
rs187621978	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5766017	GCACAATGGCTCACA[C/T]TTGTAATCCAGGAAA	54476
rs187635413	snp	A/T	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5728959	ACCAAGGCCTTTAAG[A/T]GCCATCTATTTTAGG	54476
rs187637306	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5648598	CCAGGCATGGTGGCG[A/G]GCACTCATAGTCCCA	54476
rs187640055	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5716847	TTTATTTCCATAAAC[A/C]TAACTCCAGTATTGC	54476
rs187640446	snp	C/T	0.00557542	0.0525036	intron-variant	RNF216	GRCh38.p7	7:5633128	GGGAGTACAGGCGTC[C/T]GCCCCATGCCCAGCT	54476
rs187641460	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5684328	TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG	54476
rs187715839	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620276	AGATTCCTCTCTCCA[C/G]TTTTAAGGCAAGTAA	54476
rs187786746	snp	A/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712984	TCTCTCTGCCTGTTC[A/T]TCTCTGAGAAATCAC	54476
rs187787835	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5699491	CTCCCTGCTCAAGCT[A/G]TTCTTCCCATACTGG	54476
rs187794895	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5731375	TTATTTAGCTAGCTG[C/T]CAAGCTAGACTGATG	54476
rs187802679	snp	A/G	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5687847	GACAACCCAGTGGGT[A/G]AGGCAGAGATCATGA	54476
rs187827635	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5728801	ATTTAACGGCAGTAA[C/G]AGCGACCAAGAGGAG	54476
rs187839213	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5651773	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA	54476
rs187851430	snp	A/G	0.00398564	0.0444627	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673298	CTTACGGTAATTAGC[A/G]TGGCCCTGTCAGTGG	54476
rs187863877	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5769537	AGACCAGCCTGGGCA[A/G]CATGGTGAAACGCTG	54476
rs187864084	snp	A/C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678840	CATGAGAGCTGGACT[A/C/G]GATAAATTAAGAGGC	54476
rs187871941	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5757665	ACAGTATGTATAATT[C/G]CATTTATATGAAATG	54476
rs187879791	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5742254	GTTTTGCCATGTTGG[C/T]CACGCTCGTCTCAAA	54476
rs187882270	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5731941	AGCCCCCGCCGGGGA[A/C]CCACGTCAAAGCCTT	54476
rs187892768	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5719477	TGGCTGTGCCCAAAA[C/G]CAAAGATGTTGTCAG	54476
rs187899834	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5779541	TCTCTCCCTTCTCAG[C/T]GCGTAAAGAATGTTC	54476
rs187907176	snp	A/G	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5705624	TTTAAAAAAAACTGC[A/G]GTAGGCTGGGCACGG	54476
rs187914949	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754470	ATGCCTGACTTAATT[C/G]TGGATTTTTAAGGAT	54476
rs187992131	snp	C/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5640350	TTCATGCTGTCCTCT[C/G]TCTCCCCAGCGTAGT	54476
rs187992788	snp	C/T	0.00676609	0.0577691	intron-variant	RNF216	GRCh38.p7	7:5636399	GTTACTGTTCACCAC[C/T]TGAGCTCTTACTGTG	54476
rs188000240	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666913	GCTCAAGCCTGGGCT[C/T]AAGTGATCCTGCCCC	54476
rs188021448	snp	A/T	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5698558	CCCATGCCTTATTAA[A/T]TTTTTTTCTATTTTG	54476
rs188082292	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5719001	AATGGTATAAGCACC[A/G]AGATTTATTTCAAGT	54476
rs188090285	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5747444	TACTATCCAGTCTAC[C/T]TATGGGCCAGGCAAA	54476
rs188123535	snp	A/C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5637457	GTTAGGAGCTTGTTC[A/C/T]GTGATAGAACATTCC	54476
rs188138148	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663515	CCTGAACCCGGGAGG[C/T]GGAGCTTGCAGTGAG	54476
rs188152813	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5694530	GTTCAGTTCCAACAT[C/T]TGCTATGAGATCAGA	54476
rs188172960	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5774075	AAAGAATTCTGATGA[C/T]GGAATTTCTACTCTT	54476
rs188207418	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643035	ATTTGCTTGCTCATC[C/T]GATCTGTCTGGCACT	54476
rs188212789	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5626580	AATTTAGCCAGGCAT[C/G]GTGGTGTGAGCCTGT	54476
rs188222131	snp	A/G	0.0103295	0.0711199	intron-variant	RNF216	GRCh38.p7	7:5655339	TGAAACGTCTTTTGA[A/G]AAGACTGTAGCACTT	54476
rs188227891	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668537	CACAAAGCGGACTTT[C/T]AATCTTTCCCTCCTT	54476
rs188232162	snp	A/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5710053	GCCACTGGGCAACCA[A/G]TGCAGCTGCTTTTAA	54476
rs188278335	snp	C/T	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5654026	AAAAGGTGCCAAGTA[C/T]GGAAGTAACACGATC	54476
rs188279631	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5656615	AAGTAGCCCGCCAGG[C/T]CACGTTCTTCACGTC	54476
rs188297080	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5683159	AAAAAACAGACACCA[A/C/G]ACCACAAGCTAGAAA	54476
rs188299537	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5688802	CAGTTTATTTAGCTT[C/T]CTTATTAGTGAAAGA	54476
rs188308623	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5761213	ATCTGGTCAGGGGAA[C/T]ATCTGAAGCTTATGC	54476
rs188310775	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5748213	TCTTAAACCAGTTTC[C/T]GCCAGCTTATAGAGG	54476
rs188313588	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5715449	AGTAATTCTTTATAT[A/C]AAGTTATCATATTCA	54476
rs188316853	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5717571	TGCACAAACTTATCA[C/T]GGCACTATTTATAAT	54476
rs188324614	snp	A/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5735150	GACTTCGTCTCAAAA[A/T]AAATAAATAAATAAA	54476
rs188331014	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5723718	ATTTTCCTGCATGAC[C/T]ATAAAAAGGACAGAG	54476
rs188335936	snp	C/T	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5720078	AAACAATGATTGTGA[C/T]GATGGCTCTACGACA	54476
rs188337419	snp	C/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5686269	CGTGCTTCTCCAAAC[C/T]CTCAAGAACACCACT	54476
rs188343699	snp	C/G/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5702345	AAAGTAGCTGAAATA[C/G/T]AGGGGTAAAAAACTA	54476
rs188344746	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5636957	GCAGAAGACACAGAA[C/T]GAGGAGGAGAAGAAA	54476
rs188350946	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5623839	TTGGGACTTCCTCAC[C/T]ATCAAGGAGATGCCA	54476
rs188368454	snp	A/G	4.9436e-05	0.00497148	intron-variant	RNF216	GRCh38.p7	7:5760954	TACAGCTGTGATACT[A/G]AAAGAAAAAGCCACA	54476
rs188414684	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5742707	TTCAAGCAATTATCC[G/T]GCCACAGCCTCCCGA	54476
rs188422069	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5763439	AGTTTGATACTAGCC[A/G]GGCCAACGTGGTGAA	54476
rs188460667	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5778231	ACCATTCAGTAGTAA[C/T]AATGGTTCAGTTCCA	54476
rs188473994	snp	A/C	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5765351	AATCTGTAATCCCAG[A/C]TACTTGGGAGGCTGA	54476
rs188479834	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5751231	GACACCAGAACCTAT[A/G]AAGTATATGCTGGGA	54476
rs188484607	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5689291	ATAGGAAAAGTGACA[G/T]AAGTTACGCTCAGTT	54476
rs188492517	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5706315	TCTGTTAGCAAAATG[C/T]TGTACAGCTGATCTC	54476
rs188496190	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5738043	TGTTTAAGCCAAGAT[C/G]GCACCACTGCACTCT	54476
rs188552238	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5630428	CTCAGCCCAGGGTGG[A/G]GTAAAATGGCGTGAT	54476
rs188555930	snp	A/G	0.0130921	0.0798413	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622603	AGGACTGCCGTTGGT[A/G]GCCTGGGGGATGCGA	54476
rs188558006	snp	C/T	0.000148254	0.00860844	missense	RNF216	GRCh38.p7	7:5721103	GGAAGGAGAGCACGT[C/T]GGTCATAGGACCTAC	54476
rs188558191	snp	A/C	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5646543	CTAAAAATACAAAAA[A/C]TTAGCTGGGTGTGGT	54476
rs188560299	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5656901	TCCGGCCACCACCTC[C/T]TCCAAGCCCAGCAAG	54476
rs188576534	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671576	TTGGGAGGCCAAGGC[A/G]GGCGGATCAAGAGGT	54476
rs188579870	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671243	CTGCTCATGCCTGAA[A/T]AGACTTGCCTTTGGC	54476
rs188592608	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5706040	CCTGGCTAACATGGT[A/G]AAACCCCGTCTCTAC	54476
rs188612749	snp	G/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5732154	AGAATTCAGAGTACA[G/T]TTTCCTATAAAACCA	54476
rs188620845	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5749567	TAAATTTCCTTGTCA[A/G]CTGTGTCATTATAAT	54476
rs188629095	snp	A/G	0.00119737	0.0244387	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619987	CCCAATCACTTGGAC[A/G]AATCTGTCGGCGGCC	54476
rs188644760	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673743	TTAGCTGGGTGCAGT[A/G]GTGCGCACCTGTAAT	54476
rs188647858	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5711224	AGGGAACAAAGATCT[C/G]CAACAGTAATGCACC	54476
rs188651853	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5760377	CAAAATTAGCAGGGC[A/G]TAGTGGCACATGCCT	54476
rs188661829	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5708537	TCATTCTCTTTTTCA[C/T]TTTCAGTACAGTACT	54476
rs188675564	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5734655	GAAAAATAAAAAATG[C/T]TTTAAGAGTTTGGGT	54476
rs188692225	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5661718	TGAGGCATGAGAATC[A/G]TTCGAACCTGGGAGG	54476
rs188704867	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5626186	CTATCAAAACCCCCA[C/G]ATGAGGTCATCTAGC	54476
rs188705456	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5777068	AAGTCTGAATACCCT[C/G]CTGAGAGATCACACA	54476
rs188715696	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5748578	TTCCTCAGCTTACTT[C/T]ATTATAAGAATGCAG	54476
rs188717796	snp	C/G	0.0150606	0.0854603	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5780275	AAAATGACCTGGCCA[C/G]GCTGGAGCCAGGTGC	54476
rs188717925	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5779890	CAGAGAGGAGCTGAC[C/G]GGACATACTACATCT	54476
rs188722793	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5661516	ATTTTTAAAAAAGTA[A/C]ATACGGCTGGGCATG	54476
rs188724546	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736026	TGAACCTGGGAGATG[C/G]AGGCTGCAGTGAGCT	54476
rs188724891	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767540	TAGACTCCCCAAAAT[C/T]CAACAGCAGAGAAGC	54476
rs188726632	snp	C/T	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5754965	CCTGGGAGATGGAGG[C/T]TGCAGTAAGCCAAGA	54476
rs188728650	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677225	GAGACTGCTCAGCAC[A/G]TGCTTCTGCAACATC	54476
rs188728819	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5724260	CTGATGAAGGGACAA[C/T]AGTCAGAATCTCTCT	54476
rs188739071	snp	C/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5692997	CCATTTAAGACACAA[C/T]TGTGGGCATATTGCA	54476
rs188807013	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670417	AAAAGGAGACACCCA[A/G]AACTAGAGGAGAGTG	54476
rs188863836	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5723237	TTAATTACTGTAATT[A/G]TCAATGCTACAAATT	54476
rs188869771	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664347	TACTGTCCTTCCTTT[C/G]TTTGCTCCCTAATGT	54476
rs188879262	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680577	CAGCTAATTTTTTTT[A/G]TATTTTACTAGAGAC	54476
rs188886767	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5695881	CAAGGTATCAAAAGG[C/T]TGTTTGTGTTGCACT	54476
rs188888416	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5726105	AACATGGGGACACCC[C/T]GTCTCTACTAAAAAT	54476
rs188918664	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5659653	TTGTAGGACCTTGCA[A/G]CACCCCCTTTCTAAA	54476
rs188933294	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5691513	GGAAGGCAGTGCTGG[G/T]GTGTGTAGAAGAGAA	54476
rs188947834	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5746871	GAAATTCACTTGAAT[C/T]CTAAGACTCCAAATT	54476
rs188953589	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750978	TTGCAGAGCAGACTA[C/T]TTGGTTAAAACAAGG	54476
rs188959294	snp	C/G	0.00119737	0.0244387	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5777534	TGCAGAGTTAGAGTC[C/G]ATGGGATCTGTGTAT	54476
rs188964431	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5737683	TAAGCACCTGGAAAG[A/G]GGCCCTTCCTTCTCA	54476
rs188968499	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5750665	ACACAGAGTTCACTA[C/G]GATGGCCAATGCCAC	54476
rs188974909	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5726459	CTATATCCACCCCAC[C/T]CTGTAACAGGATGCT	54476
rs188980835	snp	C/G			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713628	CTAGAGTCAAACTCA[C/G]TGGTCTATAAGCCCC	54476
rs189057874	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5628802	TGTTGGGATTACAGG[C/T]ATGAGCCATCACACC	54476
rs189067448	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5629758	CTTGAATCTGGGAGG[C/G]AGAGGCTGCAGTTAG	54476
rs189079523	snp	A/C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5634479	CCCCACCCCTTGCTG[A/C/T]CCCCAGCAACAGGAA	54476
rs189086485	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5656359	CACATTCTTCAATCT[C/G]TGGTTTACAAGAAAG	54476
rs189087910	snp	A/G	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5660637	GGTTGGAGTGTAGTG[A/G]CACAATCTTGGCTCA	54476
rs189107100	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5692381	AAGCGGTCATAGCAA[C/T]GCCGGGTGAATCAGA	54476
rs189150153	snp	C/G	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5771607	TCTGAGACCAGCCTG[C/G]ACAACATGGCAAAAC	54476
rs189159099	snp	A/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5737204	CCGCCTTGGGATGCT[A/G]TTGATCTATTACCTT	54476
rs189190300	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5740495	CTGTCCTCCATGCTT[C/G]ATGATGAGGTAAGCT	54476
rs189216164	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667902	GTCTGGGCATGGGAT[A/G]GGAAGGAGGAAGTCG	54476
rs189216295	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5634952	GGGAAAGAGTCTGGC[A/G]AGGTCCCCACCCCTC	54476
rs189222238	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5649701	TCTAAGATGCAGAGG[C/T]GATGATTCTTTCACA	54476
rs189224499	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5661295	TGCCCAGTCAGTGGC[A/G]CCAGCATAGCTCATG	54476
rs189248472	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB	RNF216	GRCh38.p7	7:5783029	ATAGAGTAAGACCCC[A/G]TCTTTACAAAAATAA	54476
rs189250574	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5764424	AGGCTGAGGAGAGCG[C/G]ATCACTTGAAGTCAG	54476
rs189263090	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768060	ATCAAGATGATTTGC[C/T]GGTACTCTAATTTGC	54476
rs189339915	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620967	ACAATCCTGTTGCTG[C/G]CGCATGGAGCCTGCC	54476
rs189350427	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5637707	ACCACCCCTGGATAA[C/G]TTTGGGATTTTTTGT	54476
rs189363874	snp	A/C			intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652088	CAACAGTTTCCTATA[A/C]CACAGACATAAGCAA	54476
rs189365137	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5649367	ACCTAGGTGACAGAC[A/G]GAGACTCCGTCTCCA	54476
rs189372414	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	RNF216	GRCh38.p7	7:5781933	CAGGTGGTTGTGGAT[A/G]TTTACTCGATATCTA	54476
rs189377946	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5652851	ATCATTAGAAGGACG[A/C]ACAAGGAAAAATTTC	54476
rs189383177	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674962	AGATCGCGCCACTGC[A/G]CTCCAGCCTGGGCGA	54476
rs189391100	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768823	CCCACCACCACGCCC[A/G]GCTATTTTTTTGTAT	54476
rs189393909	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681102	CCTCAACAGCTTGTC[C/T]CTGGCTCTTTGAACG	54476
rs189398542	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5756275	ATGGAACTGTGAGTC[A/C]ATTAAACCTCTTTCC	54476
rs189426091	snp	C/T	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5758116	CTCCAAAGTCAGTAA[C/T]TTTCCAAAATGAATT	54476
rs189440676	snp	A/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5732321	CATTACATGTGCATA[A/T]TTGATGTGGCGACAA	54476
rs189457271	snp	A/C	0.0189856	0.0955633	intron-variant	RNF216	GRCh38.p7	7:5755435	ATTAATACAAAGGGC[A/C]ATCTGTGTATAATCA	54476
rs189475792	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663883	AGCCTGGGCGACAGA[C/G]AGGGAGTCCGTCTCA	54476
rs189477953	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679341	AGTGACATATTTTGG[A/G]CAAATCCTTCAGCCC	54476
rs189481110	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5730363	TCAATTTTTCTGTAG[C/G]TTTGAAAATTTTCAT	54476
rs189539552	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5772561	ATTTTCTTTGCCTTC[C/T]TGGGAGAAACCACTG	54476
rs189551518	snp	A/C/G	0.0197834	0.0975812	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780656	CTTGCAGTGAGCCGG[A/C/G]ATCGCGCCACTGCAC	54476
rs189553217	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5760347	CGTGGAGAAACCCCA[C/T]CTCTACTAAAAATAC	54476
rs189559130	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5746679	ATAAAAACAGCATCC[C/T]TAATTTCTAAAAATT	54476
rs189610760	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5642501	ATTACAAGTGTGAGC[A/C]ACTGTGCCTGGCCTA	54476
rs189624481	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5771160	CATTGCAGAGCAGTG[A/G]AAAACATGACCTTTC	54476
rs189624649	snp	G/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5758464	CTCTTGAGCAACACT[G/T]ATTTCAACAGTGTGG	54476
rs189634470	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5744064	AAGTAACAGACAACA[A/G]AAACAAATATACAAG	54476
rs189638370	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5732377	GGTCTGTTTTTACGT[G/T]TTTTCTCAAGTAAAT	54476
rs189642824	snp	A/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5706714	TTCCCAAAGGATTTC[A/T]ATTCCTTTCCACCGG	54476
rs189649142	snp	A/G	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5721707	CCAACACCTATCATC[A/G]GTTTTTAATTTTAGC	54476
rs189661572	snp	C/G	0.0154538	0.0865337	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664942	GCTGGGATTACAGGC[C/G]CCCGCCACCAGGCCT	54476
rs189679967	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5697294	CTCTCTCATCCCACT[C/G]ATGGTCAGTTAGGGC	54476
rs189686469	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5730192	AGGGAAGTGTACTCA[A/T]GTTTTTGCAATTTAC	54476
rs189701002	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5726634	AGGCCGAGGCAGGTG[A/G]ATCACCTGAGGTCAG	54476
rs189704580	snp	C/G	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5743050	GGCGGATCACGAGGT[C/G]AGGAGATCGAGACCA	54476
rs189744325	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5639603	GTAGCTGGTATTACA[G/T]GCATCCAACACCATG	54476
rs189751255	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668323	CCGCCTCCCAGGTTC[A/G]CACCATTCTCCTGCC	54476
rs189751371	snp	A/C	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5776348	CAGCACTTTGGGAGG[A/C]CAAGGCGGGCGGATC	54476
rs189773030	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5701471	CTCACTGGGCAGCTA[C/T]TACTTCGTGACACAA	54476
rs189778092	snp	A/G	0.00636936	0.0560724	intron-variant	RNF216	GRCh38.p7	7:5776574	CACTCTAGCCTGGGC[A/G]ACAGAGCAAGACTCC	54476
rs189782055	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5645051	CGAACTCCTGATCTC[A/G]TGATCCACCTGCCTC	54476
rs189783609	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5770442	CTCCAGCCTGGGCAA[C/T]GAGAGCAAAACTCCG	54476
rs189783832	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656280	TCACAAACAAACAAA[C/T]AAAGTGCTGGGATTA	54476
rs189786315	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5763017	TGGAACAGAAACACA[C/G]AAGTTATTGATGGGG	54476
rs189792392	snp	C/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5731758	TGCAGTTCTCACACA[C/G]TTCCCTTTCTACTGG	54476
rs189796841	snp	C/T	0.0130921	0.0798413	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670036	AGTTCGAGCAATTCT[C/T]CTGTCTCAGCCTCCC	54476
rs189800780	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5687709	TCAAGAATGACAGAA[A/G]TGCCAGTGTCTTACT	54476
rs189802957	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5719118	GGGCATGGTGGTGCA[C/T]GCCTGTAACCCCAAC	54476
rs189804797	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5748983	CTCTACCAAAATATA[C/T]GAGAGAACTCTGATA	54476
rs189809269	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736399	GGTGCCGGGATTGCA[C/G]ATGGAGTCTCGTTCA	54476
rs189811242	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5704895	TGTGAATGCTGTTAT[C/T]CATAGGTGAAAGTCA	54476
rs189907907	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5639283	TCATGTGATCCTTGG[C/T]TATGATCTAGGGGTG	54476
rs189924267	snp	A/C	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5648003	GGTGGGCCACCCAGA[A/C]ACTGCATAGCTCTGG	54476
rs189940150	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5657974	CCTTGCCCTCAAGGA[A/G]TGCACTCTACTGAGA	54476
rs189947796	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672950	AAAATGTACAAAAAA[A/G]GTACTGAGATGTCCT	54476
rs189950306	snp	A/G	0.00795532	0.062565	intron-variant	RNF216	GRCh38.p7	7:5690750	CCCTTCTCTGCTGAT[A/G]CTCCTGCAATACAGC	54476
rs189955936	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5717356	GAAACTCCATCTCAA[A/C]AAACAAACAAACATA	54476
rs189992983	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5744716	GTTGGCTTATGCCTA[C/T]AATCCCAGCACTTTG	54476
rs189996051	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5655023	CCAACCCAGCCCCTT[C/T]CAGGAGTAACAGCTT	54476
rs189997320	snp	C/T	0	0	intron-variant	RNF216	GRCh38.p7	7:5764764	TGATCCCTTAAATTC[C/T]TTTTCAAGAGTAAGG	54476
rs190000417	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5762514	TTTAAAAAATAATAA[C/T]AAATAAATAAATAAT	54476
rs190014327	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5685527	AAACAGCAAGCTACA[C/T]GGTGAACTACATCAA	54476
rs190036741	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5733924	GTTTTCATTGTAAAA[A/G]TGTAGTCATTGCTGC	54476
rs190041417	snp	A/G	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5739935	TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC	54476
rs190046835	snp	A/C	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5723042	TTGAAGCCAGATTCC[A/C]AGCTGGGCTACTCGC	54476
rs190058330	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5707368	CTTGGTTAAGTTGTT[C/G]CTAAGTATTCCAACT	54476
rs190154117	snp	C/T	0.00438332	0.0466095	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621452	CACCGCGCCGGGCCA[C/T]CTTAGATCTTAGAGC	54476
rs190195498	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676080	AGTGCAACGCGATCT[C/T]GGCTCACTGTAACCT	54476
rs190231760	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5778893	GGATTACAGGCGCAC[A/G]CCATCACACCTGGCT	54476
rs190237245	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5765878	GAATTGCTTGAACCC[A/G]GGAGGCAGAGGTTGC	54476
rs190238364	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5624828	TGCTGGGAAACTCAG[A/G]GGCCACACTGGGCAA	54476
rs190241344	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754278	CTCCCATGTCAGCTT[A/C]CCAAGTAGCTAGGAC	54476
rs190244259	snp	C/G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5735367	CCAGCAGGAAGAACA[C/G/T]AATATGATTCCCAAG	54476
rs190251184	snp	C/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5733149	TTTAGTTTAGTTGTG[C/G]AGTTAACACTGTCCT	54476
rs190254824	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5654457	TTTGGGAGGCCAAGG[A/C]AGGCAAATCATTTGA	54476
rs190277346	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5650617	TTTTCCCAACTTCTA[C/T]AGGCTACCTCAATCC	54476
rs190281370	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5644783	AGTGTTGGGATTACA[C/T]GCATGAGCCACTGTG	54476
rs190285896	snp	C/T	0.00597247	0.0543191	intron-variant	RNF216	GRCh38.p7	7:5627993	GCACCTGCATAGGAG[C/T]GCGAGCCCAGGTTTC	54476
rs190326519	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5761737	GTTGCAGTGAGCCAA[A/G]ATCGTGGCACTGCAC	54476
rs190326995	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5758862	GACTTTGGGGACTGT[G/T]GGGAAGACGCAATTG	54476
rs190331052	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5777937	TAGGACAGATAAGTA[A/G]GTACATCCTCATGTG	54476
rs190426012	snp	C/G	0.00676609	0.0577691	intron-variant	RNF216	GRCh38.p7	7:5731457	CTTTGTCTATTATCA[C/G]CATGAAATACTTCCA	54476
rs190430547	snp	A/G	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5647750	CTTCCCGTATCTATC[A/G]GCTACCAAGACCTGT	54476
rs190434589	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5631951	ACGCCACGGGAGGCT[A/G]GCAAGGATTTCATAA	54476
rs190448408	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5692635	CCTTCCACACACCAC[A/G]AAACGCCATCCCTCG	54476
rs190449319	snp	A/T	0.0178098	0.0926698	intron-variant	RNF216	GRCh38.p7	7:5657576	CTGTCTAAAAAAAAA[A/T]AATAATAAAATAAAA	54476
rs190464568	snp	A/G	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5763496	TTAGCCAGGCGTGGT[A/G]GCAGGCACCTGTAAT	54476
rs190467435	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5749756	TACAAGTTTGAGTTC[A/G]TACTATCGGACTAAA	54476
rs190473844	snp	A/G			upstream-variant-2KB	RNF216	GRCh38.p7	7:5782471	ATGTCCATAATCCCC[A/G]CGCTTTGGAAGGCCA	54476
rs190501076	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5724042	GAAACTGAATCAAAT[A/G]AAATGAAGTTAATGG	54476
rs190507009	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5641791	TGTAATCCCAGAACT[C/T]TGAGAGGCCAAAGCA	54476
rs190548257	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5647078	GCTTTCAACACAATC[C/T]ACTGGGAGGCTGTTT	54476
rs190554044	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5695152	CACTTAACCTATCCA[C/T]GGTTCTTCATCTGTA	54476
rs190556301	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672201	AGGCTGTAGAGACTG[G/T]GACTAAGTCCCAGAA	54476
rs190563069	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5775477	CCTGGCTCTCCAGAA[C/T]ACTTCCTGTAAATAT	54476
rs190582006	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5748448	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATCT	54476
rs190629419	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5778494	TAATTTTGGTCTCCT[C/G]TGCTAAAACTTAAGT	54476
rs190641851	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5715369	TCTAGCTCAAGATAC[G/T]AACACAGTATTAATC	54476
rs190676652	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5631495	GGTGCTGTTCTCAGC[G/T]CACTGGTTTTGGTCC	54476
rs190710791	snp	C/T	0.0460142	0.144533	intron-variant	RNF216	GRCh38.p7	7:5765773	CACAGTGAAACCCCG[C/T]CTCTACTAAAATACA	54476
rs190715149	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753119	CAAGCAGCCCGTGCA[C/T]TTAAGCATTAAGAGC	54476
rs190716874	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5682486	GGTCTTGTCTTACTG[A/C]AACCCCTGCTTCCTG	54476
rs190719081	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5738607	CAGCTACTCGGGAGG[C/G]TGAGGCAGGAGAATG	54476
rs190721383	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5698167	CCTAGTTTTAAAATC[C/T]TCGGTTTTCTAGAAA	54476
rs190727580	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5636227	TGTTCACTTATGTGT[A/C]AAGAGCTGGCTTTCC	54476
rs190731014	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5727733	GACCCTGTTTCTAAA[C/T]AAGAATAACCATGAT	54476
rs190759349	snp	C/T	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713459	AGTCTGCATAATGAA[C/T]AGAGAACTCTCCAGA	54476
rs190788610	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5724838	CATTTTTGGGGATCA[A/G]ACCTAAATAACCTCT	54476
rs190798448	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5657297	ACTGGGCCGGGTGCA[C/G]TGGCTCACACCTGTA	54476
rs190817726	snp	A/C	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5689509	ATTTTCTAAAAAAAA[A/C]CAAAAAACAAAAAAC	54476
rs190830563	snp	A/G	0.0329836	0.124112	intron-variant	RNF216	GRCh38.p7	7:5769267	GGACTACAGGCGTGC[A/G]CCACCACGCCCAGCT	54476
rs190839115	snp	C/G	0.0023933	0.0345097	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619870	CCTAGCAGATCACCT[C/G]ATCTTCCTCCCTGGC	54476
rs190847653	snp	A/G	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5636686	GAAACGGGGCTGATC[A/G]CTGTTTTGATGGGAA	54476
rs190856421	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5693393	TGGATGCTGACCCCC[C/T]GGTATGGACCTCCAC	54476
rs190863530	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5651212	CAGGGAAGGGTGAAG[C/G]AGTTAGACAATCTTC	54476
rs190863776	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5686631	TGTCAACTATTTCTT[C/T]AAATACATGTGAGCT	54476
rs190874001	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5702886	CGACCCACTCAGCTC[C/T]GCCATTTACCATCAC	54476
rs190875611	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662780	GGAAACTAAAGCCAG[A/G]TAGGGGGCAGGCAGT	54476
rs190878305	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678003	GTAACCAGATTTTGC[A/G]ACTGTTCTTGGTATT	54476
rs190880738	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5765408	GGTGGAGGTTGCAGT[A/G]AGCTGAGATTGTGCC	54476
rs190885862	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5718118	AGGTGCAGTGGCTCA[C/T]GCCTATAATCCCAGC	54476
rs190971662	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5740624	TAGTAAGTGCCATAT[C/T]GGACAGCATAGGTCT	54476
rs190980960	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5632256	AGATCCATGACAGAC[A/C]ATGGTGCATCCCCTC	54476
rs190990725	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5693757	TGAAGCATACTGTGA[C/T]CAAATTAGGAAGCAA	54476
rs191037867	snp	C/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5734329	TAACATAATGCTGAG[C/T]GAAAAGAAATCAGAC	54476
rs191045505	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711610	TCAACCGTTACTCAC[A/C]AAGTACTCGTCCTCA	54476
rs191046111	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5723178	AATGAATTAATCCAT[C/T]AAAGCACTTAGAAAA	54476
rs191089680	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5739056	GGGTGCCACTGGCTT[A/G]GGAAGGGGATGGGGA	54476
rs191093286	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5757651	TACAAAGAATATATA[A/C]AGTATGTATAATTCC	54476
rs191097143	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677865	TACTGGAATGTAAGG[C/G]AGCTAGAAAAACAGC	54476
rs191097961	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5759355	CAATGACCAACCCCT[C/T]TTCTTCCTCCTCCTC	54476
rs191103839	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5715804	TGGAGTGCAGTGGCA[C/T]GATCTTGGCTCACTG	54476
rs191129346	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5716421	GGTTAGACATACCTC[A/G]TTAACTCTAAAGTGA	54476
rs191140168	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5697753	CTCGCCTGGAGAAGA[A/C]AGAAGCTAGGAGCAC	54476
rs191170064	snp	C/T			upstream-variant-2KB	RNF216	GRCh38.p7	7:5782816	TTATGCCACTGCACT[C/T]CAGCCTGGGTAACAG	54476
rs191199800	snp	G/T	0.0482946	0.147699	intron-variant	RNF216	GRCh38.p7	7:5639885	CTGCCTCAACCTCCT[G/T]AGTAGCTGGGACTAC	54476
rs191206391	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5653517	GAAGCAGGAGAAAGG[C/T]GTGAACCCGGGAGGC	54476
rs191222055	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665326	AAAGCCTCCCCCACC[A/T]CACTCCCTAGTCCTG	54476
rs191225681	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681908	GTGTAGCCCCTAAGG[C/G]TGGTAACCCCCAGTG	54476
rs191234092	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5748255	CTGTCTTTGTGCCCT[A/G]CAGTTCACCTTTTGA	54476
rs191238459	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5735312	TATGAGCTTAGAGTC[A/C]AATTTAGAAAATACA	54476
rs191289627	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669631	GGTGCAGTGGTTCAC[A/G]CCTGTAATCCCAGCA	54476
rs191303162	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5703371	ATTAGAGTGCTGTTA[A/G]TAAGTGCCAACCACC	54476
rs191308219	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5774562	CTATTTTTATTAACT[A/G]TTACCTGCGAAACAG	54476
rs191327340	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5761434	AATTCAATTCACAAA[A/G]AAGAAAACACAGAAG	54476
rs191334381	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5771724	ATCTCTTGAGCTCGA[A/G]AGGTGGAGGTTGCAG	54476
rs191338313	snp	G/T	0.0103295	0.0711199	intron-variant	RNF216	GRCh38.p7	7:5728206	ATGTCCCTTCCTCAG[G/T]GTGGCCCTTCTGGAG	54476
rs191341150	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5628450	ATAACTTTAATACAA[C/T]TTAAAAGTTTTTTTT	54476
rs191342965	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620529	TGGAGAACCAGGGTG[C/G]GTGCTCACGGCAGCC	54476
rs191344396	snp	C/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5745587	TAATGGTAAGGTGAT[C/T]GAGTATAAAATTAAT	54476
rs191348176	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5731090	TCAATTGGGTGTTAA[C/T]GTAATGAAGTCACTG	54476
rs191388580	snp	A/G	0.00676609	0.0577691	intron-variant	RNF216	GRCh38.p7	7:5699094	TATACAAAAGCAGAG[A/G]ATGTAATGAACCCTA	54476
rs191401110	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5777109	ACACTACACGTGGAG[A/G]GAAAGAGCCAGTGGA	54476
rs191427806	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5756927	AAGCATGAGCCACTG[C/T]GCCTGGCTGAGCTTT	54476
rs191479357	snp	C/T	0.0172553	0.0912683	intron-variant	RNF216	GRCh38.p7	7:5721213	GCATGCAGACAACTA[C/T]GTGTTAGGAACCTGG	54476
rs191481604	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750382	CAAAGCAAATTTAAA[A/T]ATGTGCTTTCAAATA	54476
rs191497972	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5623968	CTCTCCTGTGCTGGG[C/T]TGAGTGCCAGGACAC	54476
rs191504913	snp	C/G/T	0.00597247	0.0543191	intron-variant	RNF216	GRCh38.p7	7:5640365	CTCTCCCCAGCGTAG[C/G/T]AGCTAGTGTGACCTG	54476
rs191533754	snp	A/G	0.00874735	0.0655527	intron-variant	RNF216	GRCh38.p7	7:5687269	GGCATGGTGGCGGGC[A/G]CCTGTAATCTCAGCT	54476
rs191551770	snp	C/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5777477	GCCAGGAAACAAGAG[C/G]CAACAGTACCTAGGG	54476
rs191555236	snp	C/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5743755	GTCCCTAGAAGAAAG[C/G]AGATGGTGAATCTCA	54476
rs191563341	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5763830	CTTCTGCCTTGGCTT[C/T]CCAAAGTGCTGCGAT	54476
rs191565419	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5732352	ACCAGACACGGACTA[A/G]CTTTAAAATGGTCTG	54476
rs191573023	snp	C/T	0.000263539	0.0114761	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741232	TGCTGAAACAACAAG[C/T]GGCCCAGTTCTGCTT	54476
rs191575168	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5635327	ACACAATGATATTTA[C/T]GACAGTGATGAGAAA	54476
rs191594406	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5718345	GAGATCCTGCCACTG[C/G]ACTCCAGCCTGGGTG	54476
rs191612450	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656146	TGGTGGCGGGCTTCT[A/G]TAATCCCAGCTACTC	54476
rs191642275	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5640223	GTTTTTCATGTATCC[C/T]TAATCTTTGTTTATG	54476
rs191651539	snp	A/C	0.0158469	0.0875917	intron-variant	RNF216	GRCh38.p7	7:5689969	AAAAGAGAAGAGAAG[A/C]GGAGGGCAGGTAACC	54476
rs191660280	snp	C/T	0.0126979	0.078662	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666144	GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC	54476
rs191692056	snp	A/C/T	0.0291275	0.117185	intron-variant	RNF216	GRCh38.p7	7:5723625	GCACTCCAGCCTGGG[A/C/T]GACAGAGCAAGACTC	54476
rs191726246	snp	C/G	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767575	GAGCTGAGCAGAAAT[C/G]TCAGCAAACATGTAT	54476
rs191727082	snp	A/G	0.00835141	0.0640778	intron-variant	RNF216	GRCh38.p7	7:5773346	CTCCTGGGTTCAAGC[A/G]ATTCTTCTGCCTCAA	54476
rs191732600	snp	A/G	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780471	GGAGGCCGAGGCGGA[A/G]GGATCACCTGAGGTC	54476
rs191753975	snp	A/G	0.0142736	0.0832652	intron-variant	RNF216	GRCh38.p7	7:5660443	AATACAGGCGCCCGC[A/G]ACCACACCTGGCTAA	54476
rs191758908	snp	A/G	0.00279162	0.0372561	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674771	GAGGCCGAGGTTGGC[A/G]GATCACCTGAGATCA	54476
rs191768246	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5692135	GAAAAGGCTTAGCAC[A/G]GCTATTTGAAAAATA	54476
rs191768447	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5747469	GGCAAAGCCTGAAAT[A/G]TCAGACGTGACCCTT	54476
rs191774575	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5710029	AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACTG	54476
rs191777196	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5735043	CCAAGCTACTCAGGA[A/G]GCTGAGGCAGAAGAA	54476
rs191786829	snp	A/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5623736	AACACACCTGGCTTC[A/T]CTGCTTTTCAGCCTC	54476
rs191805090	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5655729	GCTCTCTCTGTGTAG[C/T]GTCTTTAAAATGTAC	54476
rs191872281	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5627544	CGAGGTCAGGAGATA[A/G]AGATCATCCTGGCTA	54476
rs191873720	snp	C/G	0.00199481	0.0315187	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663368	GGTGGATCATGACGT[C/G]AGGAGATCGAGACCA	54476
rs191878423	snp	A/G	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5646423	AGGGGGCCAGGTGCC[A/G]TGGCTCACACCTGTA	54476
rs191878580	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5629853	AAAAAAAAAAAAGAG[A/G]GAGGGAGGGTTTAGG	54476
rs191883174	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678617	AAAGGAGTGCTTATA[A/G]GGAGGCCGGCACTCG	54476
rs191885847	snp	C/G	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5763281	ATGCATTTGTCAAAA[C/G]TCACTGAACTATATA	54476
rs191889980	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5694134	ATAGTCAGTTTTACA[C/T]TATTGAGAAAAGAAG	54476
rs191890933	snp	A/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5656729	ACTTTGCAATATAAA[A/G]AAAGCACTTCCGTCT	54476
rs191907312	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712405	TTGAACTCAGGAGGC[A/G]GAGGTTGTAGTGAGC	54476
rs191912907	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712311	ATGGCAAAACCTCGT[C/T]TCTACTAAAAATAAG	54476
rs191927723	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672742	TGAGGAGGCTGCTGT[A/G]GTCTTCCTGGTGAGC	54476
rs191929934	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5778619	CTTTCAGAATAAATA[A/G]CACTCACTAATTATA	54476
rs191933722	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5653841	CAACACTCCAGACAA[C/T]GGGCAGCAAGAGAAG	54476
rs191950612	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5707043	GACTACCTTTTCCCC[C/T]GGTGGGTGTTCTTTG	54476
rs192004086	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5725534	TTAACACAGTTTCAG[C/T]TGTCTACCCAGCATG	54476
rs192054287	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673463	ACAAGAGTGACAAAG[C/G]CTCTAGAAGCCACTG	54476
rs192067779	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5708026	GCCACCATGCCCGGA[C/T]AGTGTGTTTAGTTCT	54476
rs192095688	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5752386	TTAGAAAGAGTAGTA[C/T]CATAAAAATTGCTCT	54476
rs192097486	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643715	TTTAAACCACTCTAA[C/T]GTATACAATTCAGGG	54476
rs192106791	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668961	CCACAGGGCTCTTAT[C/G]CAGCCGAAATCTAGT	54476
rs192111766	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5727368	ACTTACTAATCTATG[C/T]TTATTATTGAGTGGC	54476
rs192122604	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5700938	AGTTCTCTAGTATAG[C/T]GTATCGCCGTCTTTG	54476
rs192132043	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5648453	GGGACAGGCCAGGCA[C/T]GGTGGCTCACACCTG	54476
rs192142288	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5779863	TCAATGAATGGGCTG[A/G]GGTGGGTGGGGCAGA	54476
rs192147906	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754475	TGACTTAATTGTGGA[C/T]TTTTAAGGATGAGGA	54476
rs192151740	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5728990	ATCCTGCGGGGAGAA[C/T]GCTGGGAGCTGTCAG	54476
rs192160681	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5716911	AAGGTTACCTGTGAA[A/T]AAATTTTAAGTGGAT	54476
rs192170596	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5728840	GGTCTCTGCTGGTGC[A/G]TGCGCTCCTGTTCTG	54476
rs192175240	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5718743	GTAGAGACAGAGTTT[C/T]GCCATGTTGGTCAGG	54476
rs192186366	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675126	GTGAATTTTTTATTT[G/T]AAATAATGGCAGGGA	54476
rs192193806	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5749430	TGCTGGGATTACAGG[C/T]GTGAGCCACCACGTC	54476
rs192198841	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5710275	TGAGGCAGGAGAACT[A/G]CTTGAAGCCAGGAGG	54476
rs192211475	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5725143	GAAGAAGGAAGCCAA[A/C]AAGTGCAGCCACTTC	54476
rs192218293	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5779896	GGAGCTGACGGGACA[C/T]ACTACATCTAAAACG	54476
rs192226301	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767121	AGTATTAATAGCCTA[C/T]AGTAGACCAACCCTT	54476
rs192235715	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5633304	AGTAAGGCCGGGTGC[A/C/G]GTGGCTCATGCCTGT	54476
rs192240030	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5648642	CTGAGGCAGGAGAAC[A/G]GTGTGAACCTGGGAG	54476
rs192240549	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754830	GCCAGGAGTTCGAGA[C/T]GAGCCTGGCCAACAT	54476
rs192241635	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5659834	GGCTAACCTGCGATG[A/G]GGCAATAGCAGCACA	54476
rs192242835	snp	A/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5739776	GAGGTCGAGGCAGGC[A/G]GATCACCTGAGGTCA	54476
rs192256919	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673907	GCTCTATCGCCCAGG[C/T]TGGTGTGCACTGGCA	54476
rs192292147	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5776856	CAGTGAGCTGATATT[A/G]TGCCACTGCACTCCA	54476
rs192326556	snp	A/C			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781144	AGGCACGGCCCGCCT[A/C]CCGCCGCTCCTCCAG	54476
rs192334651	snp	A/C	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5694937	CAATATACTTTCCAA[A/C]GACCCTGGTTAACTG	54476
rs192386043	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5725932	TTTCATAAACTGGTA[C/T]GGTGGTGGAAGCAAA	54476
rs192402282	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5732026	CATATACTCTTCATC[C/T]CTAAGCTCCCCGCTT	54476
rs192403462	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5659364	TGCGACATTTAAGCT[C/G]AGTCCTAAAGGAGGA	54476
rs192404865	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5637591	TCACTCTGTCACCCA[C/G]GCAGAAGTGTAGTGG	54476
rs192407837	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5719864	TGCATAAGTGCTTTC[C/T]TCATACCTGGATATA	54476
rs192415081	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663563	CACTCCAGTCTGGGC[A/G]ACACAGCGAGACTCC	54476
rs192426227	snp	G/T	0.00874735	0.0655527	intron-variant	RNF216	GRCh38.p7	7:5690981	CCAGCACACAGCCAG[G/T]AGAGGCTGAAGCTCC	54476
rs192445103	snp	C/T	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5770822	TTTTTTTTTCTTTCC[C/T]CCCGAAACAGTGTCT	54476
rs192456985	snp	G/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652194	ATTGAATTCACAGGT[G/T]CCAGGCATTTATATG	54476
rs192466469	snp	G/T	0.00438332	0.0466095	upstream-variant-2KB	RNF216	GRCh38.p7	7:5783254	CCTGCCTCAGCCTCC[G/T]GAGTAGCTGGGATTA	54476
rs192470068	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5738399	CTGGCCCGTATTTAT[C/T]CCTTTTATAATGAAA	54476
rs192475573	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663982	ACATGGAGATGCGAT[C/G]GAGATGAAGCCTGGA	54476
rs192477697	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5769661	CCTAAGAGGCAGAAG[C/T]TGCAGTAAGCTAAGA	54476
rs192478363	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5757718	AGTGGTTTCCTTAGG[C/T]CTGGAGTGAGGTAAG	54476
rs192480009	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5680136	GGGACATCTCCCCCA[C/T]GAGCTGGCCCTGAAG	54476
rs192488217	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5695457	TGCTGCCTCGGAGCC[C/T]GGACTAAGCAAGGCT	54476
rs192490658	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713546	GGAGGCAGACTGAAT[C/T]ACCCCAGGTAAGAGA	54476
rs192491040	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5742477	AAATCTAAATCTCAT[C/T]AGTAACTAGCAAAAT	54476
rs192509960	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5632702	GAATCGCTTGAACCC[A/G]GGAGGCACAGGTTGC	54476
rs192524855	snp	C/G	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5766261	TGCCACTGCACTCCA[C/G]CCTGGGTGACAGAGT	54476
rs192534445	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5723731	ACCATAAAAAGGACA[C/G]AGGAGGGAGAACCGT	54476
rs192549380	snp	A/G	1.75693e-05	0.00296384	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739369	TAGAAACAAATAAGA[A/G]CATAATTTATATTTC	54476
rs192562144	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5654038	GTACGGAAGTAACAC[A/G]ATCAGGTATGTCTTT	54476
rs192564722	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5634215	ACCATGGGGGAAGAA[C/T]GGGTGGCTTTTCTTC	54476
rs192588759	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5692421	TGTTAGTCAGACATA[C/G]TCTGTGGGAAAAGGC	54476
rs192610581	snp	C/G	5.00438e-05	0.00500194	intron-variant	RNF216	GRCh38.p7	7:5641138	TAAAGCAATAGGCAG[C/G]CATGTGTCTACTTAC	54476
rs192617065	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5624543	TGTCTGCAGAGCCTG[A/G]AAAAGTCTTGCAGAT	54476
rs192628085	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5654136	TAGTAAAGCCACTCA[A/G]GAGAGAGGCCATGAA	54476
rs192631484	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667149	GCCCTATGGTGGGTT[A/G]TAAAGTCACTTCAGT	54476
rs192642870	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5683919	CACAGAGAATAGGGA[A/C]GGGCATCACTTGTGT	54476
rs192650664	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5699807	GACGCACATTTTCTA[A/C]CTGTGGTCTGTGGGA	54476
rs192675052	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5683590	CAAGTTTTGTGATGG[A/G]AGAGAGGTGCCAGTT	54476
rs192685235	snp	C/G	0.000280101	0.011831	intron-variant	RNF216	GRCh38.p7	7:5760965	TACTAAAAGAAAAAG[C/G]CACAGGGAAAGGGAT	54476
rs192743903	snp	G/T	0.0205511	0.0992634	intron-variant	RNF216	GRCh38.p7	7:5737020	CACCCCGTCTGGGAG[G/T]TGTTCCCAACAGCTT	54476
rs192754007	snp	A/C	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713281	ACTGAAAACAGGGAC[A/C]TGGGTGGAGCCTCTA	54476
rs192761416	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5651797	GGGATTACAGGCAAG[C/T]GCCACCATACCCAGC	54476
rs192773895	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671372	GAACTGAACTGTGTC[C/T]CCCTCAAATGCATAT	54476
rs192780558	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5758130	ATTTTCCAAAATGAA[C/T]TAGTTGTTCTTAAAG	54476
rs192803477	snp	A/T			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620202	TCTTGTTTTTATACA[A/T]AGTGACAGATCATGC	54476
rs192804657	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5758039	AAAAACAAAACTCTA[C/T]ATACCTGAAAAAAGT	54476
rs192815629	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5732188	TCATCAGTGGTAATT[C/T]TCCATCCTAGAATTC	54476
rs192833322	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5706257	GTGGTGAAAACACAC[A/T]ATACAAAAACTACCC	54476
rs192837845	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666917	AAGCCTGGGCTCAAG[G/T]GATCCTGCCCCCTCA	54476
rs192888489	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5649120	GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGTA	54476
rs192899289	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5774373	AGCCCAGGAGTTCAA[C/T]GCTGCAAGTAAGCTA	54476
rs192904048	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5691680	AAGTAGAATCTTCTA[C/T]CTGGCATGGACACAT	54476
rs192909305	snp	C/T	0.00795532	0.062565	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668011	GTTGGTATTTTAGGG[C/T]GCTGTGTAAAGATGG	54476
rs192931984	snp	C/T	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5746974	TTGAAAGATTAACTG[C/T]AAAAAGCTAATGAAA	54476
rs192943204	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5723335	TAATAAGATTTATTT[A/T]CAGTCCTTTATTTTA	54476
rs192951423	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5642160	CCGTTTATGATTTTA[C/G]TTACTCAGCAACTGT	54476
rs193008112	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5636992	AAAGTGCTGAGAATA[C/G]GCCAGACTGTTAACA	54476
rs193015909	snp	G/T	0.0314385	0.121371	intron-variant	RNF216	GRCh38.p7	7:5629611	AGGCGGGCGGATCAC[G/T]ACGTCAGGAGTTTGA	54476
rs193020296	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5742886	CAGGTGTGGGGCACC[A/G]CGCTTGGCCGATGTG	54476
rs193027315	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5720089	GTGACGATGGCTCTA[A/C]GACACTGGCCTGATT	54476
rs193036900	snp	C/T	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5688888	TACTGTGCAAAGCAC[C/T]GTGTTCTTCAATATA	54476
rs193055257	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5770175	CCATCAAACAAGATT[A/T]CTTGGGCTGGGCGCC	54476
rs193079084	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656413	CAAAGTACACTTTGA[C/T]GAGTAACCTCAAAAC	54476
rs193080157	snp	C/G	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5764481	GGCAAAACGCCGTCT[C/G]TACTAAAAATACAAA	54476
rs193086374	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5688598	AAGGCGCATGTATTT[A/G]CCAGCTTTATCCTTT	54476
rs193091619	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5737367	CTAATCTCAAGTACC[C/T]AGGGACACAAACACT	54476
rs193155774	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5654832	CTACATCCCATTCAG[C/T]AAACAAAGGTGATAT	54476
rs193157470	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5709375	CCAGCGTCACAAATT[C/T]CCCAGCCTTTGATGC	54476
rs193158805	snp	A/G	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5684429	TGGGCCTTCTAAGCC[A/G]AGCCTCTGCATTAAA	54476
rs193167664	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5760506	GGGCAATGAGTAAAA[C/T]TCCATCTCAAAAAAA	54476
rs193171865	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5734879	ATAAAAGGTTTGCAG[A/G]GCATGGTGGCTCACG	54476
rs193173399	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5625262	GAGTTGAGAGCAGCC[A/G]AGCTGGGGAGAAGGA	54476
rs193216427	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5645633	GTCTTGCTCTGTCCC[C/T]ACGCTGGTGTGCAGT	54476
rs193243185	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670835	GGGAGGAACTTGTAG[C/T]GGTGGCCATATAAGG	54476
rs193243186	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5777678	GAGAAAGAAAACGAA[A/C]ATTGTGTTAACTTTA	54476
rs193247281	snp	C/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5750728	GGAGCAAGACTCCCC[C/G]TCATAAATGTGAGAC	54476
rs193248464	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5705629	AAAAAACTGCGGTAG[A/G]CTGGGCACGGTGGCT	54476
rs199543105	in-del	-/T	0.031825	0.122064	intron-variant	RNF216	GRCh38.p7	7:5644100	GATTGAGTTTTTTTT[-/T]GCTTTTTGGCTGGTG	54476
rs199599761	in-del	-/TGT			intron-variant	RNF216	GRCh38.p7	7:5625852	GCAACAGTGGATGAC[-/TGT]ACTATTAAATTCTCC	54476
rs199612178	snp	A/C/G	1.6625e-05	0.00288309	missense, synonymous-codon	RNF216	GRCh38.p7	7:5623087	TCTGTGGCTGTGGCA[A/C/G]GTTCTGCGGAACGGG	54476
rs199633311	in-del	-/CAAT	0.00557542	0.0525036	intron-variant	RNF216	GRCh38.p7	7:5707786	TGGAGTACAGCGGCA[-/CAAT]CTCTGCTCACCGCAA	54476
rs199640368	snp	A/C/G	8.2367e-05	0.006417	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741319	AGAGACTGGAAGTAA[A/C/G]GATGATCTAACCAGC	54476
rs199654906	in-del	-/G			intron-variant	RNF216	GRCh38.p7	7:5774722	TAAAATACAGTTCAA[-/G]GGGGGGAAAAAATCT	54476
rs199668867	snp	A/G	1.67913e-05	0.00289748	missense, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712832	GTTGGGAACGAACAC[A/G]TGCAGCTGCCTTCCA	54476
rs199685797	in-del	-/A	0.0652144	0.168387	intron-variant	RNF216	GRCh38.p7	7:5652791	GAGACCCTGTCCCTT[-/A]AAAAAAAAGACAAAG	54476
rs199696428	snp	C/G	0.00299542	0.0385842	intron-variant	RNF216	GRCh38.p7	7:5690516	CTCTCCCTGCACCAT[C/G]TACCACTTAGACCAG	54476
rs199699810	in-del	-/T	0.0215465	0.101533	intron-variant	RNF216	GRCh38.p7	7:5735142	GAGAGTGAGACTTCG[-/T]CTCAAAAAAAATAAA	54476
rs199705245	snp	C/T			upstream-variant-2KB	RNF216	GRCh38.p7	7:5782720	CTGGGCATGGTGGTG[C/T]GTGCCTGTAATCCGA	54476
rs199715491	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5629459	GGGAAGATCCTGTCT[C/G]AGAAAAAAAAAAGTG	54476
rs199719941	in-del	-/C	0.110167	0.207236	intron-variant	RNF216	GRCh38.p7	7:5731728	TTTCTAAGATGACCT[-/C]CTAGGTGCTATACCT	54476
rs199768007	snp	A/G/T			intron-variant	RNF216	GRCh38.p7	7:5632005	GCAGAGAGTGGCTGG[A/G/T]CCACCAAGGTGGGCA	54476
rs199777167	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5694436	ATAACATTTGACCTT[C/T]AAATCCCTGCTTTCC	54476
rs199804558	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5642037	GACTCTATCTTAAAA[A/G]AAAAAAAAGAAAAAA	54476
rs199847664	in-del	-/AAAC	0.0146672	0.084371	intron-variant	RNF216	GRCh38.p7	7:5744639	TCTGAAGACTCTACA[-/AAAC]AAACAAACAAACAAA	54476
rs199851333	snp	C/T	0.163236	0.234461	intron-variant	RNF216	GRCh38.p7	7:5748611	TATTTTTTATATACA[C/T]ACACACACACACACA	54476
rs199886954	snp	A/G	1.65403e-05	0.00287574	intron-variant	RNF216	GRCh38.p7	7:5716675	AAGAGAAAACAGCCC[A/G]TGAAAATGCCCAGAA	54476
rs199935271	snp	C/T			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5621174	ATGGGTATCTTAGTT[C/T]TTTTTTTTTTTTTTT	54476
rs199947854	snp	C/T	1.67052e-05	0.00289004	intron-variant	RNF216	GRCh38.p7	7:5725318	CACCAACACAGTTTG[C/T]ATTACCTTGTTCAAA	54476
rs199956340	in-del	-/A			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663931	AAAAAACCCCAAAAC[-/A]AAAAAAAAAGTTCAC	54476
rs200020320	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5705922	CAACAAAAACTAAAA[C/T]AAAACAAAACAAAAC	54476
rs200027226	snp	A/G	0.000116348	0.00762629	synonymous-codon	RNF216	GRCh38.p7	7:5622902	AAAGTGCATGGGCAG[A/G]TTGTGCTCCAGGGGC	54476
rs200036930	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5690343	AAAAAAAAAAAAAAA[-/A]GATTTTAAAGATCCT	54476
rs200050294	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5647331	TTTCTTTCTTTCTTT[-/C]TTTTTTTTTTTTTTT	54476
rs200061775	snp	C/G	0.000548378	0.0165496	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752895	TCTTCATGCTGCTGA[C/G]GAGCTGGGGTGACCA	54476
rs200065272	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5721009	CCCAGAAACACACCC[A/C]AAGACCAGAGCACAT	54476
rs200074434	in-del	-/GTGGTGGT	0.00716266	0.059414	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679195	CCTCGGGTAGGGGTG[-/GTGGTGGT]GTGGTGGTGCGGTGG	54476
rs200077790	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5774190	TTTAAATCTTGGTTT[-/A]CMCMTTTAGTCAATC	54476
rs200091098	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712705	TGGCACGCTCTGCCT[A/G]AGAACGAACCTGACA	54476
rs200107868	in-del	-/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754334	AAAAAATTTTTTTTT[-/T]GTAGAGATGGAGTCT	54476
rs200117198	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5776948	AGAGAGAGAGAGAAA[A/G]AAAGAAAGAAAGAAA	54476
rs200150481	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5734883	AAGGTTTGCAGGGCA[C/T]GGTGGCTCACGTCTC	54476
rs200170526	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5637561	CATTTCTTTCCCTTT[C/T]TTTGAGACATGGTCT	54476
rs200206644	snp	A/G			upstream-variant-2KB	RNF216	GRCh38.p7	7:5782231	TGGCGGATGCCTGTA[A/G]TCCCAGCTACTCAGG	54476
rs200227974	in-del	-/T			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5621172	GAATGGGTATCTTAG[-/T]TTTTTTTTTTTTTTT	54476
rs200307481	snp	C/T	3.57258e-05	0.0042263	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739281	GTATACTTACACATT[C/T]AGATCATAATAATTC	54476
rs200333574	snp	C/G	4.94214e-05	0.00497074	synonymous-codon	RNF216	GRCh38.p7	7:5729459	TGCATAGTGTCCTTT[C/G]AGCTCGTGCAGGGCC	54476
rs200341642	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5750936	GATGGCGCTTCTTGC[C/T]TGCACACAGATAAAA	54476
rs200347536	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5773324	CTCAGCTCACTGCAA[C/T]CTCCACCTCCTGGGT	54476
rs200420546	snp	A/G	1.65124e-05	0.00287331	synonymous-codon	RNF216	GRCh38.p7	7:5623055	GAAGGGTGGGTGCGC[A/G]AAGGCATAGGGTGGC	54476
rs200428847	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5689930	GGGTGACTCTGTCTC[-/A]AAACAAAAAAAAAAA	54476
rs200431949	in-del	-/C	0.0279526	0.114869	intron-variant	RNF216	GRCh38.p7	7:5642458	ACCTCAGGTGATCCA[-/C]CTGCCTCGGCCTCCC	54476
rs200434435	snp	A/G	1.65345e-05	0.00287524	synonymous-codon, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712756	CGCAACCTCCTCCTC[A/G]GCTTTTCGCTCATAG	54476
rs200453921	snp	C/T	1.64906e-05	0.00287142	missense	RNF216	GRCh38.p7	7:5623012	TGAGTGGGAAGTTGT[C/T]GAACACAGGCCGCAC	54476
rs200498854	in-del	-/C	0.0185938	0.0946107	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5680331	AGAATGCGATCCACT[-/C]CCCCCAAGCCCAAGT	54476
rs200571402	in-del	-/A	0.0471551	0.14613	intron-variant	RNF216	GRCh38.p7	7:5657566	TCTAAAAAAAAAAAA[-/A]TAATAAAATAAAATG	54476
rs200643372	in-del	-/AAAAAAAAAAAA	0.0463947	0.145069	intron-variant	RNF216	GRCh38.p7	7:5738088	AATAAGACTGTCTCC[-/AAAAAAAAAAAA]AAAAAAAAAAAAAAA	54476
rs200688079	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5724216	AAGCTAGAGAAGGGC[A/G]CACAGGGAAGAGGAG	54476
rs200705778	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753028	GTTGGCACTATCACA[C/T]CCAACTCTTTAAGTT	54476
rs200742026	snp	A/G	0.000399281	0.0141238	synonymous-codon	RNF216	GRCh38.p7	7:5622926	CAGGGGCATGTGGAT[A/G]GGACCGAAGTCATAG	54476
rs200751710	snp	A/G	0.00199805	0.0315441	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741345	CCAGCAGTCTTCTTC[A/G]ATGGCCTGATCATCT	54476
rs200765603	in-del	-/G			intron-variant	RNF216	GRCh38.p7	7:5722377	TCTCATGTTTTTTTT[-/G]TTTGTTTGTTTGTTT	54476
rs200768498	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5683262	CTTTGTTTATTCATT[-/A]AAAAAAAAAGGGGAA	54476
rs200769983	snp	A/C/T	5.09371e-05	0.00504642	missense, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712848	TGCAGCTGCCTTCCA[A/C/T]GCAGCTGAGCTCCAA	54476
rs200811409	in-del	-/TC	0.0240643	0.107019	intron-variant	RNF216	GRCh38.p7	7:5632986	ACTGGAAGAGCACTT[-/TC]TGTTTTTTTTGAGAC	54476
rs200817631	snp	G/T	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5690534	CCACTTAGACCAGGG[G/T]AGGAGGCGCCACCTT	54476
rs200820177	snp	A/C	0.0166325	0.0896639	intron-variant	RNF216	GRCh38.p7	7:5705964	AAACAAAACAAAACA[A/C]AACACCACTCTGGGA	54476
rs200837140	in-del	-/G	0.0166325	0.0896639	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679212	TGGTGGTGCGGTGGC[-/G]GGGGGGCGGTGCACA	54476
rs200838092	snp	A/C	0.000362343	0.0134551	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741272	GTTCCTGAGGAACGA[A/C]CTGGTTTGTTATTTC	54476
rs200847164	snp	C/G/T	0.000148535	0.00861675	missense	RNF216	GRCh38.p7	7:5622942	GGACCGAAGTCATAG[C/G/T]TGACCCGCACGTTGG	54476
rs200880910	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5765968	AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAATAGA	54476
rs200881302	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5727816	CTGCCTGCCTCCTCC[A/G]CTTGGTCTTTGCATG	54476
rs200898483	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5739822	CCTGGCCAACATGGT[A/G]AAACCCCGTCTCTAC	54476
rs200911241	in-del	-/TTG			intron-variant	RNF216	GRCh38.p7	7:5722379	CTCATGTTTTTTTTT[-/TTG]TTTGTTTGTTTGTTT	54476
rs200935457	in-del	-/ACACACACAC			intron-variant	RNF216	GRCh38.p7	7:5748612	ATTTTTTATATACAT[-/ACACACACAC]ACACACACACACACA	54476
rs200945128	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5708393	ATTTGCTTCACATAT[G/T]TGGGTGCACTGATGT	54476
rs200949911	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5756006	GGCTGTGTCCCCACC[A/C]AAAATCTCATCTTGA	54476
rs200962326	in-del	-/C	0.0142736	0.0832652	intron-variant	RNF216	GRCh38.p7	7:5624979	TGGCGCTTACCTTAA[-/C]CCCCCCTCCTCAGTG	54476
rs200965513	in-del	-/GT			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754120	TTTTTCTTTTGTGTG[-/GT]GTGTGTGTGTGTGTG	54476
rs200978705	in-del	-/T	0.0322114	0.122752	intron-variant	RNF216	GRCh38.p7	7:5627743	GAGGGAGACTCTGTC[-/T]TAAAAAAAAAAAAAA	54476
rs200997201	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5740099	GTGGCTACCAGATGT[A/C]ACACCTTTTTTTTTT	54476
rs201018816	in-del	-/T	0.0854556	0.188216	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680568	CAGCTAATTTTTTTT[-/T]GTATTTTACTAGAGA	54476
rs201023713	in-del	-/TC	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5763598	TTCTTTTTGAGCCAG[-/TC]TCTCTCTGTCATCCT	54476
rs201028513	snp	A/C/T	0.000115334	0.0075931	missense	RNF216	GRCh38.p7	7:5641296	CAGCGGCAAGACATG[A/C/T]GGTTGCAGCCTTCAG	54476
rs201033964	snp	C/T	0.000399281	0.0141238	missense, intron-variant	RNF216	GRCh38.p7	7:5741718	GATTCAAATGCTGCT[C/T]TAGACTTTTTAGGCC	54476
rs201036560	snp	A/G	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5727827	CTCCGCTTGGTCTTT[A/G]CATGTCAGGAGTCCT	54476
rs201049388	snp	A/T	1.9691e-05	0.0031377	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712895	AGGCAAAGAAAAAAA[A/T]ATCAATACCATTTAT	54476
rs201054258	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5722381	CATGTTTTTTTTTTT[G/T]TTTGTTTGTTTGTTT	54476
rs201073433	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5651656	TTGCATTCTTTTTTT[C/T]TTTTTTTTTTTGAGA	54476
rs201100224	in-del	-/CTCACTGTAAGG/TTTCCTCACTGTAAGG	0.185155	0.241444	intron-variant	RNF216	GRCh38.p7	7:5734608	AACCAAATGGCTTTC[lengthTooLong]AAGGTTAAATACCCA	54476
rs201103418	in-del	-/G			intron-variant	RNF216	GRCh38.p7	7:5707719	GTGTGTGTGTGTGGT[-/G]TTTTTTTTTTTTTTT	54476
rs201146568	in-del	-/GAAG			intron-variant	RNF216	GRCh38.p7	7:5755185	AAGAGAGGAAAGGAA[-/GAAG]GAAGGAAGGAAGGGA	54476
rs201147881	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5689434	GAGGAGGCAGGGCGC[C/T]TAGAAACCCACATCC	54476
rs201149545	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5750938	TGGCGCTTCTTGCTT[A/G]CACACAGATAAAACA	54476
rs201172961	in-del	-/TTT	0.418707	0.184494	intron-variant	RNF216	GRCh38.p7	7:5774760	CCCATTCCAAGTTAC[-/TTT]TTTTTTTTTTATTGA	54476
rs201192054	snp	A/C/G	0.00015594	0.00882869	intron-variant	RNF216	GRCh38.p7	7:5725278	TGTGAAGAAGAAAAG[A/C/G]TACAGTGTTGCAGCT	54476
rs201228022	snp	G/T	0.0807149	0.183963	intron-variant	RNF216	GRCh38.p7	7:5757412	ATATATCAGCTCTTT[G/T]TGTGTGTGTGTGTGG	54476
rs201243385	snp	C/T	0.00199797	0.0315435	intron-variant	RNF216	GRCh38.p7	7:5739261	ACCACAAAAAAAGCA[C/T]GGTAGTATACTTACA	54476
rs201307797	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5739019	TAGTAGCCAAATCCA[C/T]ATAGAAAGAAAGTAG	54476
rs201325081	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5687415	AAAAAAAAAAAAAAA[A/G]AAAAAGAAAAGAAAA	54476
rs201360154	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5776966	AGAAAGAAAGAAAGA[C/T]AAAGAAAGTGAAAGA	54476
rs201372782	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5710372	CTCAAAACTTAAAAA[-/C]AAAAACAAAAACAAA	54476
rs201380992	snp	C/T	4.94768e-05	0.00497352	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741054	TTCCAAATTGGGCTC[C/T]TGAGATTCTTGCATT	54476
rs201394644	in-del	-/CA			utr-variant-3-prime	RNF216	GRCh38.p7	7:5621760	CATCTGTCAATGGGC[-/CA]GAGTGATGCCTCAGG	54476
rs201396046	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5724559	GTCATGTCAGCAGAG[-/C]CACTGCTCCACAGAC	54476
rs201399848	snp	A/G	5.83459e-05	0.00540088	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5730754	CAGACTGCTACTGGG[A/G]TTTATAATGATTCTG	54476
rs201457738	snp	A/C/G	8.25438e-05	0.00642389	missense	RNF216	GRCh38.p7	7:5623053	GGGAAGGGTGGGTGC[A/C/G]CGAAGGCATAGGGTG	54476
rs201465706	in-del	-/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768679	GTTTTTTTTTTTTTT[-/T]GGGACAGAGTCTTGC	54476
rs201467770	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5640360	CCTCTCTCTCCCCAG[A/C/T]GTAGTAGCTAGTGTG	54476
rs201470389	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5709750	TGCCCTCAGGCTTTT[A/T]TTTTTTAAATTTTTT	54476
rs201473271	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5757408	ACAGATATATCAGCT[C/T]TTTTTGTGTGTGTGT	54476
rs201478860	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5642381	ACCATGCCCAGCTAA[G/T]TTTTGTATTTTTAGT	54476
rs201594250	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5737525	ATGATCAATTAAAAA[A/T]AATAATAATAATAAT	54476
rs201641553	in-del	-/CTTT	0.0142736	0.0832652	intron-variant	RNF216	GRCh38.p7	7:5640724	ACTCACTTGGTCATG[-/CTTT]CTATTTGCTAATATT	54476
rs201643224	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5766150	AAAAAACTAGCTGCG[C/T]GGGGTGGCATGTACC	54476
rs201648752	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5690947	TGAGTCAACTTGGAC[C/T]CTGTGGTTCAGGGCT	54476
rs201660964	snp	A/G	0.000725211	0.0190284	utr-variant-5-prime	RNF216	GRCh38.p7	7:5761095	AGACATGCATATATG[A/G]GACTGCTAATATCTA	54476
rs201661041	in-del	-/AAAC	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5762694	GAGACTCTGTCTCGA[-/AAAC]AAACAAACAAACAAA	54476
rs201661241	snp	A/G	0.00137813	0.0262139	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712876	CAACTAGAAAAAGGC[A/G]AAAAGGCAAAGAAAA	54476
rs201663977	snp	A/G	0.000399281	0.0141238	missense	RNF216	GRCh38.p7	7:5721140	GTCGCTTATTTTCAA[A/G]AAAGAACATCCTCTT	54476
rs201687940	in-del	-/A	0.0475351	0.146656	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663898	GAGGGAGTCCGTCTC[-/A]AAAAAACAAAACAAA	54476
rs201691738	snp	C/T	0.000151046	0.00868908	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753026	AGGTTGGCACTATCA[C/T]ATCCAACTCTTTAAG	54476
rs201704295	in-del	-/G			intron-variant	RNF216	GRCh38.p7	7:5722402	TGTTTGTTTTGTTTT[-/G]TTTTTGAGACAGAGT	54476
rs201704800	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5755359	TTTCAAAGTATACTT[-/A]AAAAAAAAATTGAAA	54476
rs201710376	in-del	-/AACT			intron-variant	RNF216	GRCh38.p7	7:5699047	ACTTGTTTTTTTTAA[-/AACT]AACTTTTTATTGTAG	54476
rs201710919	snp	C/G	0.00199792	0.0315431	synonymous-codon, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712735	AAGCTCGTCGGCGTA[C/G]GCTGCCGCAACCTCC	54476
rs201738986	in-del	-/CTTGAA			intron-variant	RNF216	GRCh38.p7	7:5742813	GTTGGCCAGGCTGGT[-/CTTGAA]CTCCTGACCTCAGAT	54476
rs201748010	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5727905	TTTCCATATGCTGAT[C/G]ACTCTCAAAGTCCTA	54476
rs201752029	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5763115	GAGAGTAATGGGGAC[-/A]AAAAAAAACAACAAC	54476
rs201760351	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5755243	AGGGAAGGATGAAAG[A/G]AAGGAAGGAAGGAAG	54476
rs201760442	in-del	-/T	0.0154538	0.0865337	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676560	TCCGTCCTGTCTGCC[-/T]GGCTGTGTGACCAAC	54476
rs201763146	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5630384	CAATCATCTCGTACC[-/T]TTTTTTTTTCCCTCT	54476
rs201794175	in-del	-/ATC/ATCTT/ATCTTTTT			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5621171	GAATGGGTATCTTAG[-/ATC/ATCTT/ATCTTTTT]TTTTTTTTTTTTTTT	54476
rs201810333	in-del	-/A	0.0509478	0.151255	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713345	CTGAGAGAAATGAGG[-/A]AGATCTCCTGAACAG	54476
rs201821155	snp	A/G	0.000296917	0.0121807	synonymous-codon	RNF216	GRCh38.p7	7:5622953	ATAGTTGACCCGCAC[A/G]TTGGGCAGAGGGGGC	54476
rs201872284	in-del	-/T	0.0633504	0.166319	intron-variant	RNF216	GRCh38.p7	7:5688728	GTCTTATTTTTTTTT[-/T]GGACTGGGATATCTG	54476
rs201881247	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5651337	GTTCAAGCAATTCTC[C/T]TGCCTTAGCCTCCCA	54476
rs201883229	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5759718	CTCACTACAACCTCT[A/G]CCTCCCAGGTTCAAG	54476
rs201903444	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741447	TTCCAAAGGATCGCT[C/T]TCTGTGTAAAGAAGG	54476
rs201905595	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5775296	GTTCTCTCACCCAAT[C/T]TTCTGGTTTTCAAAA	54476
rs201907827	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5738733	AAAAAAAAAAAAAAA[A/T]GCTTCCATGTATTTC	54476
rs201926546	snp	A/G	0.000658696	0.018136	missense, intron-variant	RNF216	GRCh38.p7	7:5741649	TCAGAATCATCCTGT[A/G]CCCCAGAATCAAACA	54476
rs201947043	in-del	-/T	0.0115144	0.0749975	intron-variant	RNF216	GRCh38.p7	7:5623600	ACTGCACTTAGCCTC[-/T]TTTTTTTTAAAGAAA	54476
rs201968813	snp	C/T	4.94964e-05	0.00497451	missense	RNF216	GRCh38.p7	7:5623027	TGAACACAGGCCGCA[C/T]GGGAGGCAGGGGGAA	54476
rs201976922	snp	C/T			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620804	TGCCTGGGGCTCTTG[C/T]TGGAGCCACGTGCCT	54476
rs201988452	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5748607	AGTATATTTTTTATA[C/T]ACATACACACACACA	54476
rs201991571	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5772996	TGTTGGCCAGGCTAG[G/T]CTCGAACTACTGACC	54476
rs202033038	snp	C/T	3.30251e-05	0.00406343	missense, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712728	ACCTGACAAGCTCGT[C/T]GGCGTAGGCTGCCGC	54476
rs202071766	in-del	-/AAAACAAAACAAAAC			intron-variant	RNF216	GRCh38.p7	7:5705918	ATCTCAACAAAAACT[-/AAAACAAAACAAAAC]AAAACAAAACAAAAC	54476
rs202076348	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5778911	ATCACACCTGGCTAA[-/T]TTTTGTATTTTTAGT	54476
rs202085510	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5749341	TTTTTAGTAGAGACG[A/G]GGTTTCACCATGTTG	54476
rs202131937	snp	C/T	0.000164728	0.00907398	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5729544	GCTTGGATGAAGCAG[C/T]GCTGGTCAAGAGGGG	54476
rs202149734	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5624888	AGCTCCCACACCCCC[A/C]CCTGCCAGCAGACAC	54476
rs202153645	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5698904	TCTTAAAAAACTGAA[G/T]AAGCCACAAAACAGG	54476
rs202169482	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5734803	CACTCCAGCTTGGGC[A/G]ACAAGGGCAAAACTC	54476
rs202199208	in-del	-/G	0.0482946	0.147699	intron-variant	RNF216	GRCh38.p7	7:5639887	GCCTCAACCTCCTGA[-/G]TAGCTGGGACTACAG	54476
rs202237418	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5761669	CACGTGCCTGTAATC[C/T]CAGCTACTCTGGACA	54476
rs367549298	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5739838	AAACCCCGTCTCTAC[C/T]AAAAAAATACAAAAA	54476
rs367553530	snp	A/C/T			intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5780123	AATGCCAACCCAGCC[A/C/T]CTTCCAGGAGTAACA	54476
rs367554205	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5759976	AATTTACTCTCTACT[A/G]GAAAAATCATCTTTG	54476
rs367578439	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5773358	AGCGATTCTTCTGCC[C/T]CAACCTCCAGAATAG	54476
rs367599300	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5696156	ACTGACATCCACAGT[C/T]CATGTGGTGACGAAG	54476
rs367600474	snp	A/C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5714324	AGTGCAATGGCACGA[A/C/T]CTCAACTCACCACAA	54476
rs367627305	snp	C/G	3.33673e-05	0.00408442	synonymous-codon	RNF216	GRCh38.p7	7:5622896	GGGGCCAAAGTGCAT[C/G]GGCAGGTTGTGCTCC	54476
rs367637356	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5633686	GCTCAGCAGGGCGCA[G/T]AAAGAACTCAGCCTG	54476
rs367660553	snp	C/G/T	6.59875e-05	0.00574371	synonymous-codon	RNF216	GRCh38.p7	7:5715146	CGTCAGCTCCTCGAA[C/G/T]GGAAATTCCCCATAG	54476
rs367661416	snp	A/G	2.982e-05	0.00386123	intron-variant, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711713	CCATGAGGGCAGCCC[A/G]TAATACCATAATTCA	54476
rs367697176	in-del	-/ACCT			utr-variant-3-prime	RNF216	GRCh38.p7	7:5621910	TGGACAGCACCCTCT[-/ACCT]GCCTTCAGCAACCAC	54476
rs367699938	in-del	-/CA			intron-variant	RNF216	GRCh38.p7	7:5772359	AAATTCCATGGACAA[-/CA]GTTACAAAAAAACTA	54476
rs367707024	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5635650	ATGCTGCGCTGGCCT[G/T]AGGGGAGAAGGCAGG	54476
rs367737151	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665137	ATTCTTCTAACAGTG[C/T]CTTGTAATGATCTGA	54476
rs367746074	snp	A/G	3.29462e-05	0.00405857	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741154	GCAGGCTGAGGAGAA[A/G]AGGGGCCTGAAATCC	54476
rs367757777	snp	A/C	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5762713	AAACAAACAAACAAA[A/C]AAAAAATTAAAAATA	54476
rs367862979	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5740355	ATGGTCTTGATATCC[C/T]GATCTTGTGATCCAC	54476
rs367900007	snp	A/G	1.65211e-05	0.00287407	stop-gained, upstream-variant-2KB	RNF216	GRCh38.p7	7:5752965	TGATGGGCCCATCTC[A/G]GAGATTGATCCACTC	54476
rs367944850	snp	A/C/T	0.00358891	0.0422285	intron-variant	RNF216	GRCh38.p7	7:5744926	GCAGTGAGCCAAGAT[A/C/T]GCGCCATTGCACTCC	54476
rs367973890	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5698925	ACAAAACAGGACATT[C/T]GAATAAGGGTCTTTC	54476
rs367988200	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672114	GCCCCTTTGTGCACA[C/T]GCTGTGCCCTCTGAT	54476
rs368046641	snp	A/G	3.76627e-05	0.00433934	intron-variant	RNF216	GRCh38.p7	7:5740933	AGAAAAAAACTCAGT[A/G]TATGTAGTGTCTACA	54476
rs368072526	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5636685	GGAAACGGGGCTGAT[A/C]GCTGTTTTGATGGGA	54476
rs368106475	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5778889	GCTGGGATTACAGGC[A/G]CACGCCATCACACCT	54476
rs368116086	snp	C/G	6.66345e-05	0.00577172	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753010	GAACACTGTTACTGG[C/G]AGGTTGGCACTATCA	54476
rs368124283	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663562	GCACTCCAGTCTGGG[C/T]GACACAGCGAGACTC	54476
rs368130919	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5650246	GGAATCAACATATAT[C/T]ACATTTGGATGTTCT	54476
rs368131805	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5655826	TGCTCCTAAACTCAG[A/C]AAATGCTTACGCATA	54476
rs368146902	snp	C/G	3.43018e-05	0.00414122	intron-variant	RNF216	GRCh38.p7	7:5715019	ACTCCAGGAATGTGT[C/G]CTATATACATGGGAC	54476
rs368164439	snp	C/T	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5707126	CTGTATTATGTTCCA[C/T]TGGTCTACATGTCTG	54476
rs368171236	snp	C/G			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620448	CCCCAGTGCTTCTCT[C/G]CCCAATGCTGTCACT	54476
rs368195816	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5694740	CTCTGTAGCTGCGTA[A/G]CTTGTGTTGGGCTGG	54476
rs368212463	snp	C/T	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5728792	TAGAATACAATTTAA[C/T]GGCAGTAAGAGCGAC	54476
rs368225138	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5747340	GCTAACACATGGTGG[A/G]ACCAGGGGAAGGAGA	54476
rs368226571	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5710443	CTTCCCAATTGTACA[C/T]AAGCACTTTCACTGG	54476
rs368237448	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5763583	TGTAGTCTTTTTTAT[C/T]TCTTTTTGAGCCAGT	54476
rs368272649	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5723047	GCCAGATTCCCAGCT[A/G]GGCTACTCGCTAGCT	54476
rs368275619	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5689980	GAAGAGGAGGGCAGG[C/T]AACCCCCCTTATTTG	54476
rs368278117	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675150	GCAGGGAACAATGTA[A/G]TGATTCTGGAACGCT	54476
rs368288850	in-del	-/G			intron-variant	RNF216	GRCh38.p7	7:5761657	GGGCGTGGTGGCACG[-/G]TGCCTGTAATCCCAG	54476
rs368300262	in-del	-/GT			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754119	TTTTTCTTTTGTGTG[-/GT]GTGTGTGTGTGTGTG	54476
rs368304531	snp	C/G	1.64773e-05	0.00287026	synonymous-codon	RNF216	GRCh38.p7	7:5652505	CTGACACTTCCTACA[C/G]GTTTCCTGGGGATAA	54476
rs368341086	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5640258	CATTTGCCAGTGAGA[A/C]TTTATTATTTTTTAG	54476
rs368341165	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5648501	GAGGCCAAGGCAGGC[A/G]GATCATGAGGTCAGG	54476
rs368342313	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5775494	CTTCCTGTAAATATG[C/T]CTGCCACTTCTGCAA	54476
rs368350646	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621378	GGGGACTCAAACTCC[C/T]GACCTCAACTCATCC	54476
rs368356343	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5634061	GCAGCCACAGGCTGA[A/C]TGTTCCCAAAATAAC	54476
rs368395602	in-del	-/GGAA	0.0372196	0.131242	intron-variant	RNF216	GRCh38.p7	7:5726933	TACCTGATTTGAAAC[-/GGAA]GGAAGGGTGTGTGAG	54476
rs368403959	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5715555	ATGAGAGATGTTACC[C/G]AAAAAACTTTCAAAA	54476
rs368418624	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5723758	CCGTGTCTCACTCTT[C/T]GAGTCAAGCAATTAT	54476
rs368434165	snp	A/C/T	6.58896e-05	0.00573943	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741256	TCTGCTTCAGGCTGC[A/C/T]GTTCCTGAGGAACGA	54476
rs368497514	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5707384	CTAAGTATTCCAACT[A/T]TTTTGATGTATTATA	54476
rs368506692	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5695272	ATACAAAACCACCTG[C/T]GCAGACCCAGTGCAG	54476
rs368529869	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5731957	CCACGTCAAAGCCTT[C/T]TCCCTCATCCTGACA	54476
rs368556994	in-del	-/G			intron-variant	RNF216	GRCh38.p7	7:5687415	AAAAAAAAAAAAAAA[-/G]AAAAAGAAAAGAAAA	54476
rs368557518	snp	A/C/T	0.000126288	0.00794552	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712875	CCAACTAGAAAAAGG[A/C/T]GAAAAGGCAAAGAAA	54476
rs368570210	snp	A/G	4.94703e-05	0.0049732	synonymous-codon	RNF216	GRCh38.p7	7:5622971	GGGCAGAGGGGGCAC[A/G]TACGGGGCTGGGATA	54476
rs368602855	snp	C/T			synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739314	AAAATGAATTATTTC[C/T]TCAATAAACCCATTT	54476
rs368607128	snp	C/T	0.000115642	0.00760314	intron-variant	RNF216	GRCh38.p7	7:5729389	TACCATGGGAAGATG[C/T]AGTCAAGAGGTGTGA	54476
rs368627248	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5749540	CAGTCATAATTTTGG[C/T]TCAGAAATAACTAAA	54476
rs368649118	snp	C/G	1.64727e-05	0.00286986	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741533	TTGCTGCTTGGTTAT[C/G]ACTCGGTCCAGGCTT	54476
rs368657376	snp	A/T	0.000153988	0.00877328	intron-variant	RNF216	GRCh38.p7	7:5716709	ACAAGGTGAGATTTC[A/T]AACTACCTTTTGATA	54476
rs368696627	in-del	-/AAGT	0.00199481	0.0315187	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669895	TCTCAAAAAAAAAGA[-/AAGT]AAGTGAGATTGTGGA	54476
rs368717706	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673752	TGCAGTGGTGCGCAC[C/T]TGTAATTCCAGCATT	54476
rs368727020	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5642153	AGTACATCCGTTTAT[G/T]ATTTTAGTTACTCAG	54476
rs368737146	in-del	G/TT			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676027	TTCTTTTTTCTTTTT[G/TT]TTTTGAGACAGAGTC	54476
rs368756889	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682444	AGACAGTCTCACTCT[A/G]TTGCCCAGGCTGCAG	54476
rs368761941	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5683763	CACAGCAGTAGATAA[G/T]CAATGAGCCATACAA	54476
rs368777880	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678096	ATGTGCACTCCAATG[C/T]CTGACGCCCCACTGT	54476
rs368788748	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5624202	GACAGTGAGGAGGCC[A/G]CTTGTTGCTTATGGC	54476
rs368790474	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5699245	ATCTTTTCATTTATA[A/T]ATATTTCAGTTTGTA	54476
rs368801323	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670728	TCGTAACACAGTATG[C/T]TGAAATGTGACTTCC	54476
rs368805744	in-del	-/T	0.00835141	0.0640778	intron-variant	RNF216	GRCh38.p7	7:5693396	ATGCTGACCCCCCGG[-/T]ATGGACCTCCACTGT	54476
rs368808928	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5651802	TACAGGCAAGCGCCA[C/T]CATACCCAGCTAATT	54476
rs368829873	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5726600	CGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT	54476
rs368862069	snp	A/G	0.000153988	0.00877328	intron-variant	RNF216	GRCh38.p7	7:5641392	CTGAAATAAGAAAAC[A/G]TAATTTGGAGCTGGG	54476
rs368886188	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667391	AAAAGGCACCAAAAG[C/G]CTCATTCTCACAATA	54476
rs368892755	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5760577	ACATGTTCCAAAATT[C/G]CCCTCAAGGCTAAGC	54476
rs368908632	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5746951	AACAGAATTCTAAAA[C/T]AGCTTTTTTGAAAGA	54476
rs368928882	snp	A/C/T	0.000115521	0.00759923	intron-variant	RNF216	GRCh38.p7	7:5716788	AACAAAAAAGGCACA[A/C/T]ATTCAGACACAAATT	54476
rs368933437	in-del	-/AA	0.494976	0.0498674	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768295	GTCGCTATTAGGGGG[-/AA]AAAAAAAAAAAAAGG	54476
rs368939552	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5660813	GGAGTCAAGCAATCC[A/G]CAAGCTTCAGCCTCC	54476
rs368994120	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5717075	AAAACTAAGTTTGGC[C/T]GGGTGGGATGGCTCA	54476
rs368999130	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673068	CGACTCAGGGTGGTG[A/G]GGGCCTATGTGCACG	54476
rs368999318	snp	C/T	0.000102347	0.00715283	intron-variant	RNF216	GRCh38.p7	7:5624007	GCCAGCAGAAGCCTG[C/T]ATGGCCTGGCTGCTG	54476
rs369010110	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5729279	CATTTAGTCCGTCAC[A/G]ATGAGCAAATACCCA	54476
rs369013998	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5742393	ACAAAAATAACTCCA[C/T]AGCAGATACAACAAT	54476
rs369048691	in-del	-/AA/AAA	0.49655	0.04139	intron-variant	RNF216	GRCh38.p7	7:5765952	GTGAGACTCTGTCTC[-/AA/AAA]AAAAAAAAAAAAAAA	54476
rs369065974	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5723016	AAAAGCACGTGGTTA[C/G]ACAGTAAGCTTTGAA	54476
rs369112711	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5645963	TTTAGTTCTTTGCCC[A/G]TGGTTTCACCTGGCT	54476
rs369168799	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5638684	GCTCTGTCACCCAGG[C/T]TACAGTGCAGTGGCA	54476
rs369172733	snp	C/T	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5740018	AAAAAAAAAACAAAC[C/T]AAAAACAAAACAAAA	54476
rs369184855	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5723926	ACTACTAATGTAAAT[C/G]AAGTGTAATTTCTAT	54476
rs369207621	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5747787	AAAAGGGGAAAAAAA[A/T]AGAAAAAATAAATAA	54476
rs369224651	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5701821	ACACTTCTCACGTAA[C/G]GGCTTCAAAAGAACT	54476
rs369226029	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5764120	TGCTTCAACCAGGGA[A/G]GCAGAGGTTGTAGAG	54476
rs369237265	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5763640	CAGCTACACGATCAC[G/T]GCTCACTACAGCCTT	54476
rs369275264	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5772021	GGTGGATCACCTGAG[C/G]TCAGGAGTTCGAGAC	54476
rs369293438	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5726171	TGGTCCCAGGTACTC[A/G]GAGGCTAAGATAGGA	54476
rs369343110	snp	A/G	1.65002e-05	0.00287225	synonymous-codon	RNF216	GRCh38.p7	7:5623028	GAACACAGGCCGCAC[A/G]GGAGGCAGGGGGAAG	54476
rs369346660	snp	C/T	0.000189794	0.00973967	intron-variant	RNF216	GRCh38.p7	7:5725286	AGAAAAGGTACAGTG[C/T]TGCAGCTACACACTG	54476
rs369357994	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674770	GGAGGCCGAGGTTGG[C/T]AGATCACCTGAGATC	54476
rs369415799	snp	C/G/T	0.000310705	0.0124606	intron-variant	RNF216	GRCh38.p7	7:5730673	AACAACAAAGCACAG[C/G/T]ATTTCCAGGCAGTGA	54476
rs369421499	snp	C/G/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665972	AGATCGAGACGATCC[C/G/T]GGCTAACACGGTGAA	54476
rs369422539	snp	C/G/T			intron-variant	RNF216	GRCh38.p7	7:5692564	GAGCTTGTGCTGCAA[C/G/T]CAGAGCCCGTGCAGA	54476
rs369425608	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5704526	TCTAAATGCACGTAG[C/T]GATTTGCTTTGGTAC	54476
rs369433049	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5701436	TCATCTCCTGAGGCC[A/G]CACATCTGCACACAC	54476
rs369439165	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5660494	ACAGGGTTTCACCAT[C/G]TCGGCCAGGATGGTC	54476
rs369443623	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5737357	TCACCACTCCCTAAT[C/T]TCAAGTACCCAGGGA	54476
rs369516612	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5721938	TTTATGATTTTCTTT[C/T]TGGAGACAGAGCCTT	54476
rs369520677	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5688823	TAGTGAAAGAGTTGC[C/T]CTTAATAATATGATA	54476
rs369540679	in-del	-/CA			intron-variant	RNF216	GRCh38.p7	7:5704953	TGTAATCATAACACA[-/CA]TTCTCTCCACTGCAA	54476
rs369547541	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5658144	CTTCATGGGATTGAC[C/T]ACAGTAAGTGCCATG	54476
rs369572162	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5693393	GGATGCTGACCCCCC[-/C]GGTATGGACCTCCAC	54476
rs369598430	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5720308	GACCATGAAGATAAA[-/A]GACCTTCTCATGCTG	54476
rs369608894	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5641678	TACCCTGGCATAGTG[C/T]CCAGTACTCAGCATT	54476
rs369621756	snp	C/G			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712234	CCTGTAGTCCCAGCA[C/G]TTTGGGAGGCTGAGG	54476
rs369628982	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5650932	TTCATTTTCTGAGTA[C/G]CAAACTCCTTCCATA	54476
rs369631890	snp	A/G	1.80422e-05	0.00300346	intron-variant, nc-transcript-variant	RNF216, MIR6874	GRCh38.p7	7:5711842	ACAGGACGGGCACCT[A/G]GAGTCAGAACAGCAG	54476
rs369650904	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5725651	GGTCAGGAGTTCGAC[A/C]CCAGTCTGGCCAACA	54476
rs369658960	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5742021	TAGTCATTCATAGAT[A/T]AAAGCTTGAGATATA	54476
rs369680360	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5751117	GGTGTGCTGTGCACC[C/T]TCAGAAAGTTTTAAA	54476
rs369720329	snp	C/G	1.64762e-05	0.00287016	missense	RNF216	GRCh38.p7	7:5641207	GGCAAGGGGCTCCTG[C/G]TGAGCGGGGATGTTG	54476
rs369753877	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5640821	TGTTAGGGCTATCTC[C/T]GTCAGGCTTTGGAAT	54476
rs369771777	in-del	-/TT			intron-variant	RNF216	GRCh38.p7	7:5653628	AAAAAAAAAAAAGAA[-/TT]AAAAAAAAATGTTAA	54476
rs369778446	snp	C/G/T	5.63537e-05	0.00530794	intron-variant	RNF216	GRCh38.p7	7:5624155	ATGAGAAGGATGAAC[C/G/T]TGTAGCTTCATGCAG	54476
rs369780264	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5642430	TGTTGGCCAGGCTGG[G/T]CTGGAACTCCCGACC	54476
rs369833191	snp	A/G/T	6.58892e-05	0.00573936	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741270	CCGTTCCTGAGGAAC[A/G/T]ACCTGGTTTGTTATT	54476
rs369842222	snp	G/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670054	GTCTCAGCCTCCCGA[G/T]TAGCTGGGATTACAG	54476
rs369865768	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5707781	CAGGCTGGAGTACAG[C/T]GGCACAATCTCTGCT	54476
rs369886319	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5735267	AAAGCAATAATCTCT[A/G]AAGAAACCAACTCTA	54476
rs369892501	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5708514	CTGTAATTCAAGTAC[C/T]CATACAATCATTCTC	54476
rs369916775	in-del	-/GACT			intron-variant	RNF216	GRCh38.p7	7:5626409	AGGCCTAAGAAAAAA[-/GACT]AAAAAAAAAAAAAAG	54476
rs369945377	snp	A/T	5.23775e-05	0.00511723	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739359	TCTTGCTTCCTAGAA[A/T]CAAATAAGAACATAA	54476
rs370004752	snp	G/T	1.67902e-05	0.00289738	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752879	ATCATCCAGGTCCTC[G/T]TCTTCATGCTGCTGA	54476
rs370006041	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5704314	TATTACTGGCAAAGA[C/T]ACTGCAATGAGAAAG	54476
rs370008302	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5761825	TTCAAACCACTGGGG[G/T]GGCAAAAAAGGCAAG	54476
rs370038009	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671613	TTCGAGACCAGCCTG[A/G]CCAACATGGTGAAAC	54476
rs370055013	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5686179	AGTGAGCCGAGATCA[C/T]GCTGCTGCACTCCAG	54476
rs370069485	snp	A/T	0.000153988	0.00877328	intron-variant	RNF216	GRCh38.p7	7:5721209	AAAAGCATGCAGACA[A/T]CTATGTGTTAGGAAC	54476
rs370077844	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5760393	TAGTGGCACATGCCT[A/G]TAATCCCAGCTACTC	54476
rs370092618	snp	A/C	1.68678e-05	0.00290407	intron-variant	RNF216	GRCh38.p7	7:5725479	CCTTCTGTAAATAGA[A/C]AATAAGAATACACGA	54476
rs370098025	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781668	GGCCCTGCCGCGGCG[C/T]CACCTCGCGCCTGCG	54476
rs370109940	in-del	-/AGTG	0.342806	0.232136	intron-variant	RNF216	GRCh38.p7	7:5756113	TTCTGCTCTCGTGAT[-/AGTG]AGTGAGTCTTGAGGT	54476
rs370158829	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5718153	TGGGAGGCCAAGGTG[C/G]GGGGATTGCTTAAGG	54476
rs370178502	snp	C/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753324	TCTCTATTCCTCCTG[C/G]GAATAAATGTCTATT	54476
rs370185183	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5771081	AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCA	54476
rs370187514	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5744848	GTGGTAGCGCATGCC[C/T]GTAATCCCAGTTATT	54476
rs370192981	snp	A/G			upstream-variant-2KB	RNF216	GRCh38.p7	7:5781737	AGAGGCACTCCGGGT[A/G]CTGCGGAGGAGGGAC	54476
rs370226254	snp	A/G	0.000572686	0.016912	synonymous-codon, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711779	TCGGCAGTGAGGATT[A/G]GGACAGCTGAACCTC	54476
rs370235293	in-del	-/CCATCA			intron-variant	RNF216	GRCh38.p7	7:5640686	ATTGTTAATATTAAA[-/CCATCA]TTGCATTTCTAGAAC	54476
rs370240192	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5644245	TCTATGTTTAACTTA[C/T]TGGGGAAAGCCAACT	54476
rs370242659	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5682941	GAAAAAAATTCTACA[C/T]TTCCAACTCAGGAGC	54476
rs370246545	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5651534	ACCCTGCCCGGCTGT[C/G]AGACAATCTCTGAAT	54476
rs370281330	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5736111	AATAAATAAATAGCT[C/T]TCCCTCTCCCTGTCC	54476
rs370288793	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5722550	CGCCCGCCACCATGC[C/T]CGGCTAATTTTTTGT	54476
rs370328786	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5728346	GCACTGTGGGAGGCT[A/G]AGGTGGGCAGATCAT	54476
rs370335998	snp	A/T	3.31038e-05	0.00406827	intron-variant	RNF216	GRCh38.p7	7:5716665	AAAACATGGTAAGAG[A/T]AAACAGCCCATGAAA	54476
rs370378342	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5658057	GTGCACGCACACACG[A/G]CAGGGGAGCATGCAT	54476
rs370379222	in-del	-/AG			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768687	TTTTTTTTTTGGGAC[-/AG]AGTCTTGCTCTGTCG	54476
rs370421138	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5647443	GGTTCAAGGGATCCT[C/T]CTGCCTCAGCCTCCC	54476
rs370425106	snp	A/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681327	CATCATTTACCTGTT[A/T]TAGGAAAAAATACAA	54476
rs370438662	snp	A/C/T	0.00279258	0.0372817	intron-variant	RNF216	GRCh38.p7	7:5703010	GGGAGCGTCCTTCTG[A/C/T]GGCCTGAACCTGAAG	54476
rs370440591	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5626533	ACCAGCCTGGGCAAC[A/T]AAGTGAGATCCTATC	54476
rs370442254	in-del	-/CTTTCCTCCGTTGCTCATCACT	0.0142736	0.0832652	intron-variant	RNF216	GRCh38.p7	7:5653136	GGCTCCTAAGGGAGA[-/CTTTCCTCCGTTGCTCATCACT]CATCGGCATGGATGT	54476
rs370443740	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5630236	CAGTGCTGGCTTCTT[C/T]AAGAGAGGCTGCTGG	54476
rs370471300	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666356	TCACGATTATAAACT[A/G]GTGGTCAGGGAAGGC	54476
rs370474613	snp	A/C	0.000153988	0.00877328	intron-variant	RNF216	GRCh38.p7	7:5652539	ACAGACACAAAGACA[A/C]CTCCTGGTGAGTGGA	54476
rs370504464	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5738480	TTGGGAGGCCGAGGC[A/G]GGTGGATCACGAGGT	54476
rs370506256	in-del	-/T	0.0414363	0.137845	intron-variant	RNF216	GRCh38.p7	7:5639408	ACACTTCTGTTTTCC[-/T]TTTTTTTTTGAGAAC	54476
rs370515697	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5773662	AACCTCCGTCTCCCA[A/G]GTTCAAGCGATTCTC	54476
rs370535577	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5737961	GACAGGGTGGAGTAC[C/G]CCTGTAATGCCAGCT	54476
rs370556781	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5716327	CCAGCCTGGCCAACA[C/T]GGTGAAACCCCGTCT	54476
rs370576171	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5714118	CAGGCACCCACCACC[A/G]CACCTGGCTAATTTT	54476
rs370584066	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5634600	GAGCAGAGACTTCAC[C/G/T]GGCTCAGGGCTGGCC	54476
rs370599339	snp	A/C	5.50585e-05	0.00524654	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622824	ACACTCCTACCCCAA[A/C]CGGGCTTTGTGCTGC	54476
rs370615006	in-del	-/AC			intron-variant	RNF216	GRCh38.p7	7:5748612	ATTTTTTATATACAT[-/AC]ACACACACACACACA	54476
rs370619106	snp	A/G	5.473e-05	0.00523087	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622838	AACGGGCTTTGTGCT[A/G]CTCAATGGGGATTCG	54476
rs370635603	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5705560	AGACTTTGTTCTCAC[C/T]CATGCTGCACATCCC	54476
rs370641671	snp	C/T	0.000477842	0.0154497	intron-variant	RNF216	GRCh38.p7	7:5721014	AAACACACCCCAAGA[C/T]CAGAGCACATCTTCC	54476
rs370642635	snp	C/G/T	3.35397e-05	0.00409499	intron-variant	RNF216	GRCh38.p7	7:5725469	AATTGGTAGTGGCA[C/G/T]	54476
rs370648716	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5738774	GTGGTTGCAGAACAT[G/T]TTGTTACAATCGTAG	54476
rs370661308	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5758997	CAATGTTGGAGATGC[A/G]GCCTGGTGGGAGGTA	54476
rs370668691	snp	C/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5748400	AAGTAGCTGGGATTA[C/T]AGGTGCTCACCACCA	54476
rs370669567	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5693338	AGTCTGCTGACCCCT[A/G]GTATGGATGTTTACA	54476
rs370674291	snp	C/G	4.94328e-05	0.00497131	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741077	CTTGCATTGGAAAGG[C/G]TGGACCTGGCTCTTC	54476
rs370682550	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5775793	AGAAATGCTTGAACC[C/T]GGGATGCAAAGCTTG	54476
rs370686230	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667967	GTTCCAGGGTACAGC[A/G]CAGCTTCAAGCTGAG	54476
rs370699538	in-del	-/CAAA			intron-variant	RNF216	GRCh38.p7	7:5744654	AAACAAACAAACAAA[-/CAAA]AAACAACCCTCGAAG	54476
rs370702417	snp	C/G	1.64746e-05	0.00287002	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741370	TCATCTGCTAGAGCA[C/G]CTGACTCTCCTAGAT	54476
rs370707197	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5728033	TACTCAGATGTCTCA[C/T]AGGCCCTTCTCAGCA	54476
rs370727623	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5723340	AGATTTATTTTCAGT[C/T]CTTTATTTTAAAAAA	54476
rs370732553	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668519	TGAGCCACCGTGCCA[A/G]GCCACAAAGCGGACT	54476
rs370743255	snp	A/C/G	2.03718e-05	0.00319147	intron-variant	RNF216	GRCh38.p7	7:5624175	GCTTCATGCAGTGCT[A/C/G]AGGCCCCGTGGGACA	54476
rs370744030	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5758453	TACACAGTTGACTCT[C/T]GAGCAACACTGATTT	54476
rs370754982	snp	C/G	1.66846e-05	0.00288826	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741014	GCTCTTGATCTACCT[C/G]TGCAGCTTCTTGCCC	54476
rs370757776	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781554	ACTCGTCACTCAAGT[C/T]GCCGGCTAGCCAGGC	54476
rs370777954	snp	A/G	0.000437904	0.0147905	intron-variant	RNF216	GRCh38.p7	7:5716644	TTTGCCATCAAAAAT[A/G]CTGACAAAACATGGT	54476
rs370785821	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5723173	ACATAAATGAATTAA[C/T]CCATTAAAGCACTTA	54476
rs370824818	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663974	TCTGTGCCACATGGA[A/G]ATGCGATGGAGATGA	54476
rs370833339	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5742811	ATGTTGGCCAGGCTG[C/G]TCTTGAACTCCTGAC	54476
rs370835718	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5761354	AAGAGACAAAGTACT[A/G]ACAGAGAAATGACAT	54476
rs370837902	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5765710	TACTTCGGGCGGCTG[A/C]GGCGGGCAGACTGCC	54476
rs370843939	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5776643	GGGCAGGTAGTCAGT[A/G]AAGGTTTCACAGGAA	54476
rs370874433	in-del	-/AAA	0.0182019	0.0936463	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667322	CTATAGGTCACAAAC[-/AAA]AAAGTTTAAAAGCCA	54476
rs370892902	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5733663	AGGAAAACATTAACC[-/A]AAAAAAAAAAAAAAA	54476
rs370921000	snp	C/G	3.29788e-05	0.00406058	intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652383	GAAGTTGAGAATCAG[C/G]CCATAGCCCCTCTGA	54476
rs370931481	snp	C/T			upstream-variant-2KB	RNF216	GRCh38.p7	7:5782733	TGCGTGCCTGTAATC[C/T]GAGCTACTCGGGAGG	54476
rs371017395	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5747517	ATGTTTCAGCTCTAC[A/G]GTGTTATCTGAAAGC	54476
rs371040185	in-del	-/G			intron-variant	RNF216	GRCh38.p7	7:5723029	TAGACAGTAAGCTTT[-/G]AAGCCAGATTCCCAG	54476
rs371069800	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671564	AATCCCAGTACTTTG[A/G]GAGGCCAAGGCGGGC	54476
rs371091782	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5639925	CCACCACGCCCGGCT[A/C]ATTTTTTGTATTTTT	54476
rs371105465	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5744048	AAAATCAAAACAAGA[C/G]AAGTAACAGACAACA	54476
rs371114894	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5776879	GCACTCCAGCCTGTG[C/T]GACAGAGGGAGACTC	54476
rs371128240	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5765567	CCCAGGAGTTCGACA[A/C]TGCAGTGTGCCACCA	54476
rs371149121	in-del	-/ATTG			intron-variant	RNF216	GRCh38.p7	7:5715686	GTAATGTACCAGGCT[-/ATTG]ATTGACTCCTTTTAT	54476
rs371156952	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5627834	GAGAGGCTCTCTTTT[G/T]GGGAGAAGAGCTCTG	54476
rs371232219	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5635416	ACTCTTTTGTAGAAT[A/C]AATTTTTAAGGTTAA	54476
rs371245595	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5733621	TACATTTTCTGTAAT[A/G]AACAAACCTGTATTA	54476
rs371247645	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5752610	GTTGTAGCAATGACA[A/G]CAGTGGAATTTGGTG	54476
rs371252112	snp	A/G			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622440	TTCCCAGGCCCGCAG[A/G]TGCAGCCCCCTCTGC	54476
rs371261520	snp	A/G	1.64781e-05	0.00287033	intron-variant	RNF216	GRCh38.p7	7:5760979	GCCACAGGGAAAGGG[A/G]TGAAGTGAGAACAAA	54476
rs371280334	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671247	TCATGCCTGAATAGA[C/T]TTGCCTTTGGCTCAT	54476
rs371328318	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5736520	CAAAGTGCCGAGATT[G/T]CAGCCTCTGCCCGGC	54476
rs371333445	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5771394	CATAAAAGAAAAAAC[A/T]GAAACACTATACATT	54476
rs371431845	snp	C/G/T	0.000115306	0.00759223	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741623	GATCCAGAAATTCAC[C/G/T]GTAGTCATCCTCAGA	54476
rs371438133	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5715845	CTCCCAGGTTCAAGC[G/T]ATTCTCCTGCTTCAG	54476
rs371438892	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5716406	CCCATCTTGCCCTGA[A/G]GTTAGACATACCTCG	54476
rs371454649	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5749823	GTAACTGCTAACCAA[A/G]ATCAAACAGCAAAAA	54476
rs371459722	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5625252	GGTCCTCCAGGAGTT[A/G]AGAGCAGCCGAGCTG	54476
rs371465610	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5766422	ATGGTATTTGGAGAT[A/G]GAGTCTGTGGGAGGT	54476
rs371465679	snp	A/G	3.79889e-05	0.0043581	intron-variant	RNF216	GRCh38.p7	7:5752814	TCACCAACTTGCAAT[A/G]ATGTCTCATTGTAAG	54476
rs371481169	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5629397	TAGAGCCCAAGGAGG[C/T]TGAGGCTGCAGTGAG	54476
rs371482772	snp	A/G/T	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622518	TGCTACCCAGGGGTC[A/G/T]GCTCCGAGGAGAGGC	54476
rs371488828	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5654225	GGGAGGAAGTAAGAC[C/T]GGTGGGTGTAGAGAT	54476
rs371491830	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5688267	AAAATGTAACTAGAC[A/G]GTAAATTGAGCCAAG	54476
rs371499485	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5727600	ATCCAGGTGTGGTGG[C/T]GTGCACCTGTAGTCC	54476
rs371504867	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671705	AGCTATTTGGAAGGC[C/T]GAGGCAGGAGAATCT	54476
rs371506682	snp	G/T			intron-variant, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711390	AAATGGCAAAAGGTG[G/T]GTGTGTGGGGAGGGA	54476
rs371531838	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671209	GCTGGAAATCCTGAT[C/G]AACACAGAGGGGACC	54476
rs371533313	snp	C/G/T	3.29453e-05	0.00405854	synonymous-codon, missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741252	CAGTTCTGCTTCAGG[C/G/T]TGCCGTTCCTGAGGA	54476
rs371536469	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5749261	GTTTAAGCGATTCTA[A/C]TGCCTCAGCCTCCTG	54476
rs371558326	snp	A/C/G	3.29506e-05	0.00405884	missense	RNF216	GRCh38.p7	7:5721112	GCACGTCGGTCATAG[A/C/G]ACCTACAATGTCGTC	54476
rs371573304	snp	C/T	0.000153988	0.00877328	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741042	CCCCCAAATGTTTTC[C/T]AAATTGGGCTCTTGA	54476
rs371579896	snp	A/G	1.67209e-05	0.00289139	synonymous-codon, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712822	CAGCTCACTGGTTGG[A/G]AACGAACACGTGCAG	54476
rs371634763	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5717301	GAGGTTGCAGTGAGC[C/T]GAAATCGCACCATTG	54476
rs371647103	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5702946	GGCTGCTGTGGGGAC[C/T]AATATGAGCTGAGAG	54476
rs371686018	snp	C/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780999	CAGCCCCCAGCGCCC[C/G]GCAGAAGGGTTTGAC	54476
rs371692506	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5755981	TACTGTCTATAGATT[C/G]ATATGGTTTGGCTGT	54476
rs371711295	snp	C/T	4.98037e-05	0.00498993	intron-variant	RNF216	GRCh38.p7	7:5721201	GACAATGCAAAAGCA[C/T]GCAGACAACTATGTG	54476
rs371726176	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5739891	GCCTGTGATCCCAGC[A/T]ACTCGGGAGGCAGAG	54476
rs371759259	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5624807	TGCAGGCAGATGTGG[A/G]AGCTGTGCTGGGAAA	54476
rs371780795	snp	G/T			utr-variant-3-prime	RNF216	GRCh38.p7	7:5621356	ATTTTGTATTTTTAG[G/T]AGAGACGGGGACTCA	54476
rs371828670	snp	C/T	6.86648e-05	0.00585898	intron-variant, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711752	CTAGAAAAAAATGTG[C/T]CTCCCTACCTTTCGG	54476
rs371833754	snp	C/T	4.94507e-05	0.00497221	intron-variant	RNF216	GRCh38.p7	7:5652525	CCTGGGGATAAAGGA[C/T]AGACACAAAGACAAC	54476
rs371836824	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5660196	GGGCTCAAGCGATCT[A/G]CCCACCATGGCCTCC	54476
rs371866654	snp	C/T	0.00119737	0.0244387	intron-variant, nc-transcript-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666679	AGGTGGGGCCTCTCC[C/T]GCCTTCCTGCCGAGC	54476
rs371899345	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5695527	AGTGCCTCTCCCTGC[C/T]GGTCTCCTGCTCTCT	54476
rs371908440	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5774734	TCAAGGGGGGAAAAA[-/A]TCTTTATTTTCCCAT	54476
rs371909272	snp	C/T	0.000181316	0.00951973	synonymous-codon, intron-variant	RNF216	GRCh38.p7	7:5741705	GCTGCTCTTATCTGA[C/T]TCAAATGCTGCTCTA	54476
rs371911172	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5776519	AGAATGGCGAGAACC[C/T]GGGAGGCGGAGCTTG	54476
rs371969166	snp	C/G	3.87034e-05	0.00439889	intron-variant, nc-transcript-variant	RNF216, MIR6874	GRCh38.p7	7:5711855	CTAGAGTCAGAACAG[C/G]AGAACTGACATTACT	54476
rs372013197	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5733020	TTAAAATGGCCAGAC[C/G]GTTCCATCTGAAGGC	54476
rs372026770	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5631163	TACTCAAGGAAACAA[A/C]CAGCCAAAACGCAGA	54476
rs372046703	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669064	TAGAGAGTATTTCAA[C/T]GCAGGCAGGTGGCTA	54476
rs372052687	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5650702	CCTTCTCACGTTTGT[C/T]TGACTCTTCGTCCCA	54476
rs372057838	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665634	CCACACATAGCTGCC[A/G]GCTTTTTACTATACT	54476
rs372074665	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5706934	AATCCATTTAAAGAG[C/T]TGATTTTTGTGTTAT	54476
rs372081090	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5655322	GTCCCGGAGAACATA[C/T]CTGAAACGTCTTTTG	54476
rs372092181	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5658394	GGGCACAGTGGCTCA[A/T]GCCTGTAGTCTCAGC	54476
rs372096400	snp	A/C/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5726052	GAGGATGACGGGGGT[A/C/G]GATCACTTGAGCTTA	54476
rs372108527	snp	A/G	4.94181e-05	0.00497057	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741257	CTGCTTCAGGCTGCC[A/G]TTCCTGAGGAACGAC	54476
rs372112026	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5659919	AAAGGGACTTTATTA[A/C]TATTCTTCTTAATAT	54476
rs372140840	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673076	GGTGGTGGGGGCCTA[C/T]GTGCACGGTGTGGGC	54476
rs372152768	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670051	CCTGTCTCAGCCTCC[C/G]GATTAGCTGGGATTA	54476
rs372161549	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5683995	AGGGGTCTTGTGGCG[C/G]GATGTGTGAAGACCA	54476
rs372177142	in-del	-/AAAAAAAAAAA			intron-variant	RNF216	GRCh38.p7	7:5687404	CACCTCAAAAAAAAA[-/AAAAAAAAAAA]GAAAAAGAAAAGAAA	54476
rs372200929	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5734653	TTGAAAAATAAAAAA[A/T]GCTTTAAGAGTTTGG	54476
rs372213799	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5693002	TAAGACACAATTGTG[A/G]GCATATTGCACCCAT	54476
rs372227558	in-del	-/CAGTCCCATG	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5635155	GAAAGCACTGCCTCC[-/CAGTCCCATG]CAGTAAAAATCACAC	54476
rs372237798	snp	A/G	1.64741e-05	0.00286998	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5729537	GTCAGCAGCTTGGAT[A/G]AAGCAGCGCTGGTCA	54476
rs372242149	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5736198	TACTGCTGCCATCTC[G/T]GCTCACTGCAACCTC	54476
rs372260373	snp	A/G	0.000153988	0.00877328	missense	RNF216	GRCh38.p7	7:5652413	AATTCTGTTACTCAC[A/G]TAGAGGTACGGTACT	54476
rs372287066	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5645614	TTTTTTTTTTTGCAA[C/T]AGAGTCTTGCTCTGT	54476
rs372299694	snp	C/G	0.00993419	0.0697739	intron-variant	RNF216	GRCh38.p7	7:5707207	GAGGCTTCCAGCTTT[C/G]TTCTTCTTTCTTAAG	54476
rs372318107	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5742107	GCTGGAGTGCAATGG[C/T]GCGATCTCGGCTCAC	54476
rs372336440	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5745657	GTAATCTCAGCACTT[C/T]GGGAGGCTGAGGTGG	54476
rs372347863	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5778128	ACCATGGTGAAACCG[A/C]AATCCTTACCATGGC	54476
rs372374639	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5720272	CAACACACCCCTCCT[-/T]CCTCAGCCTACTCAA	54476
rs372380804	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5774995	GTGATCCACCCCCCC[-/C]GACACTCACCAAAGT	54476
rs372395928	snp	A/G	0.000257984	0.0113545	synonymous-codon, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711770	CCCTACCTTTCGGCA[A/G]TGAGGATTAGGACAG	54476
rs372434713	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5630278	GAACTACAACTCTGG[A/G]GCTCCAGACCTGGCT	54476
rs372499106	in-del	-/AAACAAAACAAAACAAAACA			intron-variant	RNF216	GRCh38.p7	7:5705949	AAACAAAACAAAACA[-/AAACAAAACAAAACAAAACA]CCACTCTGGGAGGCC	54476
rs372528580	snp	A/G	0.000133893	0.00818099	intron-variant	RNF216	GRCh38.p7	7:5624040	CTGTCCTGGGGGCCT[A/G]GGGAGGGGCACTTGC	54476
rs372530732	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5728862	CCTGTTCTGGCCACA[A/G]CTACAAAGCAGGCAC	54476
rs372547256	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5702215	GCTGCAGCAGCCCTG[A/C]AGAGGGAGTGGGAGT	54476
rs372548325	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5777658	CAAAGCAGATGATGA[A/G]TTCAGAGAAAGAAAA	54476
rs372548954	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672536	ACAGGAGATGGACTT[C/T]GAATTGATGTTCTGA	54476
rs372567291	snp	A/G	0.0142736	0.0832652	intron-variant	RNF216	GRCh38.p7	7:5737875	TGAGCAGATCATGAG[A/G]TCAGGGTTTCAAGAC	54476
rs372611045	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5773004	AGGCTAGTCTCGAAC[C/T]ACTGACCTCTGGTGA	54476
rs372656015	in-del	-/G	0.478437	0.10157	intron-variant	RNF216	GRCh38.p7	7:5642046	TTAAAAAAAAAAAAA[-/G]AAAAAAAAAAAGAAA	54476
rs372675901	in-del	-/AAAC			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675663	AACAAACAAACAAAC[-/AAAC]GAACAAAGGAGCAAG	54476
rs372686370	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5728591	AAAAAAAAAGAAAAA[A/G]AAAAAGAAAAAGAAA	54476
rs372693334	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5764223	ATTAAAAAAAAAAAA[A/C]AACAGATAAGTATCC	54476
rs372700256	snp	A/T	0.00016512	0.00908475	intron-variant	RNF216	GRCh38.p7	7:5729404	TAGTCAAGAGGTGTG[A/T]CCCCAACAGGAAGAC	54476
rs372706082	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5686272	GCTTCTCCAAACTCT[C/G]AAGAACACCACTGCT	54476
rs372711319	snp	A/G	9.2477e-05	0.00679926	intron-variant	RNF216	GRCh38.p7	7:5730687	GCATTTCCAGGCAGT[A/G]ACTGCAAAACATGAA	54476
rs372724830	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780455	AGACTGTAGCACTTT[A/G]GGAGGCCGAGGCGGA	54476
rs372733247	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5689362	CATATTTGTAGTATT[-/A]AAAAAAAAAAAAAAA	54476
rs372742316	in-del	-/TTTTTTTT			intron-variant	RNF216	GRCh38.p7	7:5644828	TTTTTTTCTTTTTTT[-/TTTTTTTT]GAAACGGAGTCTTGC	54476
rs372746288	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5697312	GGTCAGTTAGGGCCG[C/T]GGTTGCCCTTTCTCT	54476
rs372752732	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5743428	TTGTCCCTGAGTGAA[A/T]GGTTAAATAAACTAT	54476
rs372763748	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5629495	AACTGAATTGTAAAC[C/T]TAAAAATGGCAAATT	54476
rs372766874	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5708118	AGATACTTGGTATGA[C/T]TTTGATCTTAAATTT	54476
rs372767554	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5765457	CAACAGGGTGAGACT[C/T]CATCTCAAAAAATAA	54476
rs372771049	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5758065	AAAGTTCTCATGATG[A/G]GTGCAGAGTATACAT	54476
rs372775923	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5624183	CAGTGCTGAGGCCCC[A/G]TGGGACAGTGAGGAG	54476
rs372791347	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664673	CAGGGGCTGTGGAAG[A/G]CCAGTTGCCGCCCAA	54476
rs372814651	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5634262	TCCCCTTAGAAAGCT[G/T]ACTGGGAATTGCAAG	54476
rs372834686	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5763586	AGTCTTTTTTATTTC[C/T]TTTTGAGCCAGTCTC	54476
rs372835427	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675055	CGGTACAGAATGGCA[A/G]CTGCTGAAAAGCCAG	54476
rs372838930	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664454	TGTGAGAAAGTACTG[C/T]ATATGTTTCAATTAG	54476
rs372846913	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5634618	CTCAGGGCTGGCCCT[A/G]GCTTCTGCAGCCACC	54476
rs372865139	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652227	AGTTTGTCTTCTGAA[A/G]TAACTCCATGAGGCT	54476
rs372881443	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5642017	CAGCCTATGTAACAG[A/C]GTGAGACTCTATCTT	54476
rs372890069	snp	C/T	0.00795532	0.062565	intron-variant	RNF216	GRCh38.p7	7:5726686	AACATGGCAAAACCC[C/T]GTCTCTAGTAAAAAT	54476
rs372892308	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5742683	TCACTCCAACTTCTG[C/T]CTCCCAGGTTCAAGC	54476
rs372913117	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5709749	GTGCCCTCAGGCTTT[A/T]ATTTTTTAAATTTTT	54476
rs372933892	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5776468	GGCGTGGTGGCGGGC[A/G]CCTGTAGTCCTAGCT	54476
rs373019151	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680748	ACCCCAGACAAAAGA[C/T]GTCTGAAGCACCACT	54476
rs373054401	snp	A/G	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5633697	CGCAGAAAGAACTCA[A/G]CCTGACACAGAAGAC	54476
rs373091885	snp	C/T	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5733424	TTGATTACGTTTTAG[C/T]GATTTTTCTAGACAA	54476
rs373109444	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5776686	GCTAAAGTGAGAGAC[A/G]TGTCAGATCTGGGTT	54476
rs373182101	snp	G/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670230	TGAGCTACCGTGCCT[G/T]CCCTGGAAATCACTT	54476
rs373190471	in-del	-/TCGG			intron-variant	RNF216	GRCh38.p7	7:5655748	TTAAAATGTACTCTC[-/TCGG]TCTTCTAAACAGTGT	54476
rs373222000	snp	A/C/G	4.94189e-05	0.00497062	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741307	GGCTGTTGGTTCAGA[A/C/G]ACTGGAAGTAAGGAT	54476
rs373238422	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5736008	TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGA	54476
rs373266864	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5656889	TAGACAAATGTATCC[C/G]GCCACCACCTCCTCC	54476
rs373291151	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5760412	TCCCAGCTACTCAGG[A/C]GGCTCAGACCGGAGA	54476
rs373311978	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5748314	AATGCTGAAACTCTA[C/T]CCCAGGGAAGCTCTG	54476
rs373322433	snp	A/C	0.00438332	0.0466095	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739429	CAAGACAGATGGCAA[A/C]AAGTATAATAAAATG	54476
rs373324407	snp	A/C	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5695229	ATCTAACATCTACAA[A/C]TGCAAGTCAAGAGTA	54476
rs373353973	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671897	GCACGAAGACAGTCC[C/T]CTGCAAGCCAAGGAG	54476
rs373371049	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5696082	CTGACTCCCAGGAGG[C/G]ACGGAAGGACAAGAA	54476
rs373382119	snp	C/T	1.64768e-05	0.00287021	intron-variant	RNF216	GRCh38.p7	7:5721028	ACCAGAGCACATCTT[C/T]CTACCTCTGCCATCT	54476
rs373383311	snp	C/T	3.29766e-05	0.00406045	missense	RNF216	GRCh38.p7	7:5716723	CAAACTACCTTTTGA[C/T]ACTGTTCTTCATTCA	54476
rs373383588	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5733134	AGTTTCCATTAACAT[G/T]TTAGTTTAGTTGTGG	54476
rs373399603	in-del	-/CTCT			intron-variant	RNF216	GRCh38.p7	7:5714765	AGGCTGCAAGGTTCT[-/CTCT]TTCTGAGGTAACCTT	54476
rs373416089	snp	C/T	0.000395289	0.0140531	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741385	GCTGACTCTCCTAGA[C/T]TTGATAACAGCTCTG	54476
rs373443789	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5680224	CTGTGTCCTCTTCCG[C/G]AAGTCTCTTCATGCT	54476
rs373476928	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5697868	AGGGCTGTGGGAACA[C/T]GAGATGTTTTTAGCA	54476
rs373481679	snp	C/T	1.7967e-05	0.0029972	intron-variant	RNF216	GRCh38.p7	7:5740970	TGATAAAATAAAACT[C/T]ACCGTTTCTTTCACT	54476
rs373482307	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5747525	GCTCTACGGTGTTAT[A/C]TGAAAGCAAAATAGA	54476
rs373497223	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5779419	TCCCCACACCCCAGG[A/C]GCAATAAATTATGAA	54476
rs373531497	in-del	-/GG			intron-variant	RNF216	GRCh38.p7	7:5707717	TCAGTGTGTGTGTGT[-/GG]TTTTTTTTTTTTTTT	54476
rs373552715	snp	C/T	3.31417e-05	0.00407059	missense	RNF216	GRCh38.p7	7:5641353	TGGCATTTTCTAATG[C/T]GGGCAGCAGTCATTT	54476
rs373574460	in-del	-/TGAGGCAATCCCTG	0.0142736	0.0832652	intron-variant	RNF216	GRCh38.p7	7:5655486	GCCTGTAATCCCAGC[-/TGAGGCAATCCCTG]TGAGGCTGAGGCAGG	54476
rs373598166	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5751745	CACTTCTCCTCAGCT[C/G]AGTGGAACACCTACT	54476
rs373625414	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5639782	TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT	54476
rs373629144	in-del	-/GGG			cds-indel	RNF216	GRCh38.p7	7:5623082	GGCATCTGTGGCTGT[-/GGG]GGCAGGTTCTGCGGA	54476
rs373633089	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5704667	ACCTAGTGGCAACTC[A/G]TTCCACAGCCCACAA	54476
rs373670774	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5683412	TTCCTGCAACAGTGC[C/T]CAGAGGTGTCTATAT	54476
rs373726004	snp	A/C/G	0.00318978	0.0398085	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674952	CAGTGAGCTGAGATC[A/C/G]CGCCACTGCACTCCA	54476
rs373733949	snp	A/C/T	9.17534e-05	0.00677272	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622825	CACTCCTACCCCAAA[A/C/T]GGGCTTTGTGCTGCT	54476
rs373744722	snp	C/T	0.000153988	0.00877328	intron-variant	RNF216	GRCh38.p7	7:5624166	GAACCTGTAGCTTCA[C/T]GCAGTGCTGAGGCCC	54476
rs373747364	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5638455	TCAAGTACACGCACT[A/C]CATCTTCGGATCTGT	54476
rs373749391	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673322	TCAGTGGAGCTGCTG[C/T]TCAAGAACAGGCTCG	54476
rs373758114	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5628763	TGGGCTCAAGCGATG[C/G]ACCCAACCTTGGTCT	54476
rs373785974	snp	C/G	0.000153988	0.00877328	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741113	CACTTGCTAACTGCT[C/G]GTCTTCAAACTCTCC	54476
rs373787213	snp	A/C			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620556	AGCCCTGTGGTCCCC[A/C]GTGCCTGGCTCGGGG	54476
rs373834108	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5639706	CTCAGGTGATCCACC[C/T]GCCTTGGTTTCCCAA	54476
rs373836043	in-del	-/G			upstream-variant-2KB	RNF216	GRCh38.p7	7:5783576	ACAATAGTCTTGATG[-/G]CGGCAATGAGTGTTC	54476
rs373847772	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5747796	AAAAAAAAGAAAAAA[A/T]AAATAATAACTAGAT	54476
rs373851144	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5758634	TAAGATTTAATGACC[A/G]CCCTGCTGGGTTTTG	54476
rs373854509	snp	C/G	0.000239267	0.0109351	intron-variant	RNF216	GRCh38.p7	7:5725297	AGTGTTGCAGCTACA[C/G]ACTGCCACCAACACA	54476
rs373855177	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5731702	TCTGTTCTTTCTCTT[A/G]CTCCAGTAGATTTCT	54476
rs373884421	snp	C/G/T	3.29746e-05	0.00406035	missense	RNF216	GRCh38.p7	7:5641326	GATTTGATGAGGCCA[C/G/T]TCCCACACTTGTGGC	54476
rs373889912	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5723418	TTTGGGAGGCCGAGG[C/T]GGGCGGATCACGAGG	54476
rs373892123	snp	A/G	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5738569	CAAAATTAGCCAGGC[A/G]TGCTGGCAGGCGCCT	54476
rs373928316	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5630037	CTTGGAAAAAGGCCA[C/T]GCTACAAATCTAGGA	54476
rs373969635	snp	C/T	6.68527e-05	0.00578117	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752886	AGGTCCTCTTCTTCA[C/T]GCTGCTGAGGAGCTG	54476
rs374043397	snp	A/G	0.000153988	0.00877328	intron-variant	RNF216	GRCh38.p7	7:5725484	TGTAAATAGAAAATA[A/G]GAATACACGAGACAG	54476
rs374045755	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5626203	TGAGGTCATCTAGCC[G/T]CTTTGTGAACACTCC	54476
rs374050276	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753430	TTGCTCATCTTAAAC[A/C]CAAACTTTAAGAATC	54476
rs374062269	snp	A/G	3.30164e-05	0.00406289	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712691	GAAGAGTTGGCAGAT[A/G]GCACGCTCTGCCTGA	54476
rs374072181	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5661083	TAGCTGGAATTACAG[C/G]TATGCACCACCATGC	54476
rs374080529	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5697243	GACCCATGTCGCTCA[A/T]GCAGAGCCGCATGTT	54476
rs374104480	in-del	-/GTGTGT			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754120	TTTTTCTTTTGTGTG[-/GTGTGT]GTGTGTGTGTGTGTG	54476
rs374179885	in-del	-/GGAAACTG	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5746585	TTGACTGAGTCAGAT[-/GGAAACTG]GGAAACTGCAAAGTG	54476
rs374184702	snp	A/C	0.000193127	0.00982477	intron-variant	RNF216	GRCh38.p7	7:5739234	TACATATATTTTACC[A/C]CCACCACCACCACCA	54476
rs374223757	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5735351	CTAGGCACCATGGGA[A/G]CCAGCAGGAAGAACA	54476
rs374227655	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5709456	GAACTGTTCTCTCTA[C/T]GGGAAAAAGAGGGTC	54476
rs374240472	in-del	-/GAGT	0.0345262	0.126772	intron-variant	RNF216	GRCh38.p7	7:5648711	CCAGCCTGGGTGACA[-/GAGT]GAGACTCTGTCTCAA	54476
rs374242402	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5749775	TATCGGACTAAATAT[C/T]CAAAATTCTAATGAA	54476
rs374248478	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677723	CATTCTCCACTTCCT[A/G]TGCAGAGTCCTGGGA	54476
rs374248715	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5630085	GAGAGGGGAAAAATA[A/G]AAGGAAAGAGGATGA	54476
rs374249947	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5727300	TCACCACCTCACCCT[C/T]ATGACCACAAGCTTT	54476
rs374251836	snp	C/G	0.000153988	0.00877328	missense	RNF216	GRCh38.p7	7:5721059	CTTTGATTTTCTGCT[C/G]ATAGAACTCCTGCTC	54476
rs374252404	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5646482	GCAGATAATGAGGTC[C/T]GGAGATCGAGACTAT	54476
rs374254297	snp	A/C	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5743271	GTCTCAAATAAATAA[A/C]TAAATACACAAATAC	54476
rs374254730	snp	C/G/T	0.00011531	0.00759236	missense	RNF216	GRCh38.p7	7:5721056	TCTCTTTGATTTTCT[C/G/T]CTCATAGAACTCCTG	54476
rs374256724	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5699114	AATGAACCCTATGCA[C/T]CCATTATCGTGTTTA	54476
rs374258339	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5736028	AACCTGGGAGATGGA[A/G]GCTGCAGTGAGCTGA	54476
rs374263582	snp	C/G	4.98136e-05	0.00499042	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5752995	CTACAGGAAAGCAGA[C/G]AACACTGTTACTGGG	54476
rs374264565	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5771529	CGGCGGGGTGCAGTG[A/G]CTCATGCCTGTAATC	54476
rs374272752	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5627724	TGCACTCCAGCCTGG[C/T]GACAGAGGGAGACTC	54476
rs374280986	snp	A/C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5762737	AAAAATACAGTATGC[A/C/G]TAAGAATGACCTCAG	54476
rs374288672	snp	A/G	7.42129e-05	0.00609105	intron-variant	RNF216	GRCh38.p7	7:5623228	ATTAAACCAACCTCA[A/G]TGGAATCTAGCCTGG	54476
rs374289769	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5734179	AGAATGTTCACAGCT[A/G]CATTATTTGTGACAG	54476
rs374294468	snp	C/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753042	ATCCAACTCTTTAAG[C/T]TTTTCCTGACAGGGG	54476
rs374314379	snp	A/C			utr-variant-5-prime, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781717	CTAAGGACAGGAAGA[A/C]CCATAGAGGCACTCC	54476
rs374351343	snp	A/G	0.000288281	0.0120024	splice-donor-variant	RNF216	GRCh38.p7	7:5730713	ATGAACATGACACTT[A/G]CCTTTGTCTCATCTT	54476
rs374355925	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675076	GAAAAGCCAGCTTCA[C/T]ATGTAACTAAAGCAG	54476
rs374357653	snp	A/C	1.67379e-05	0.00289287	intron-variant	RNF216	GRCh38.p7	7:5725465	GAAAAGGAAAGGTTC[A/C]TTCTGTAAATAGAAA	54476
rs374367071	snp	A/G	0.000164715	0.0090736	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741624	ATCCAGAAATTCACC[A/G]TAGTCATCCTCAGAA	54476
rs374369090	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5644511	TGATATTGTTTGCCC[A/G]TTTTTTTTTTTTGAG	54476
rs374369120	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5718255	GCATGGTGGGGCGCA[C/G]CTGTAATCCCAGCTA	54476
rs374370298	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5654379	CTTCTGGTGGGATGT[A/C]GTAAAAAGCCTCAAT	54476
rs374412126	snp	A/G	8.23635e-05	0.00641677	synonymous-codon	RNF216	GRCh38.p7	7:5652436	ACGGTACTTGATGTC[A/G]TCTTTTTCAGCCAGC	54476
rs374418266	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5648014	CAGACACTGCATAGC[C/T]CTGGGTGTTTTGTAA	54476
rs374431242	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5725755	CTCAGGAGGCTGCGG[A/C]AGGAGAATCGCTTGA	54476
rs374433921	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5727804	CCTCCTTCCTGTCTG[C/T]CTGCCTCCTCCGCTT	54476
rs374453807	snp	G/T	0.00015097	0.0086869	synonymous-codon	RNF216	GRCh38.p7	7:5623082	TGGCATCTGTGGCTG[G/T]GGCAGGTTCTGCGGA	54476
rs374456589	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5736252	CCTGCCGAGTGCCTG[C/T]GATTGCAGGTGCGCG	54476
rs374463957	snp	A/G	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5633524	AGGCTGCAGTGAGCC[A/G]AGATCACATCACTGC	54476
rs374465376	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754886	TACAAAAATTAGCCG[A/G]GTGTGGTGGCATGCA	54476
rs374471258	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RNF216	GRCh38.p7	7:5783425	GCGAGCCACTAAACC[C/T]GGCCAGAGGATTGTT	54476
rs374481544	snp	A/G	1.65493e-05	0.00287652	stop-gained, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712764	CCTCCTCGGCTTTTC[A/G]CTCATAGTACTTATA	54476
rs374494024	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5632756	CATTCCAGCCTGGGC[A/G]ACAAGAGCAAAACTC	54476
rs374504035	snp	A/G	0.000484228	0.0155525	intron-variant	RNF216	GRCh38.p7	7:5730832	TCTGCAGAAACAAAT[A/G]ATGTTACTTTCATAC	54476
rs374521552	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5693840	CAAAGACAGAGATGG[A/G]CGCGGGTAGAGACTC	54476
rs374521899	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5737385	GGACACAAACACTGC[A/G]GAAGACCCCAGGGTC	54476
rs374536048	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674560	TTAAGCCCAGGAGGT[C/T]GAGGCTGCAGTGACC	54476
rs374574709	in-del	-/TG			intron-variant	RNF216	GRCh38.p7	7:5757423	TTTTTGTGTGTGTGT[-/TG]GTGGCTATTTGCATG	54476
rs374586124	snp	C/G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5748404	AGCTGGGATTATAGG[C/G/T]GCTCACCACCATGCC	54476
rs374590754	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5759106	TGGTTGTTTAAAAGT[G/T]TGTGGCACCTCTTCC	54476
rs374616288	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5695897	GTTTGTGTTGCACTG[-/C]AAAGACTAAGCAGAG	54476
rs374622115	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5623486	TTTTTTTTTTTAATA[G/T]ATGGGGTTTTGCCAT	54476
rs374635180	snp	A/C	0.0126979	0.078662	intron-variant	RNF216	GRCh38.p7	7:5710381	TAAAAACAAAAACAA[A/C]AACAAAAAACGTCCT	54476
rs374638417	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5648864	AATCTCATTTGGATC[C/T]TAACCTGAACAAACT	54476
rs374664542	snp	A/C			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682319	ACACCCGTCCCTCTA[A/C]AAGGGCAGCCATGGA	54476
rs374698335	snp	C/T	9.34868e-05	0.00683627	intron-variant	RNF216	GRCh38.p7	7:5752826	AATAATGTCTCATTG[C/T]AAGTTTAAAGAAAAC	54476
rs374713560	snp	C/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780674	CGCGCCACTGCACTC[C/T]AGCCTGGGCAACAGA	54476
rs374729014	in-del	-/ACT			intron-variant	RNF216	GRCh38.p7	7:5751825	AACTGGGATCTTTAA[-/ACT]AAAAAAAAAAAAAAA	54476
rs374743185	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5750510	ATGCCTGTTATTTAG[A/G]TTGCAGCACTGTTCA	54476
rs374759095	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5758066	AAGTTCTCATGATGG[G/T]TGCAGAGTATACATA	54476
rs374763668	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5715341	AATGATATGCTGTTT[C/T]GTGCTATATAAATCT	54476
rs374804188	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5694404	AATCTATTCTGACCA[C/T]GAGCACTATCTGGGT	54476
rs374809313	snp	C/T	0.000197827	0.00994356	synonymous-codon	RNF216	GRCh38.p7	7:5721150	TTCAAGAAAGAACAT[C/T]CTCTTTTCTATTTTT	54476
rs374810205	snp	C/G	0.000131776	0.00811608	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741499	ACTTTCTGCTCTGAT[C/G]TGGGGTTGACAATGT	54476
rs374814239	snp	C/T	1.68917e-05	0.00290613	synonymous-codon	RNF216	GRCh38.p7	7:5623106	CTGCGGAACGGGCCT[C/T]GGGAGGGCCTCCACC	54476
rs374828959	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5764807	TGCAGTGGCTCATGC[C/T]TATAATCCCACCACT	54476
rs374834777	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5635867	AACCAAATGGCTAGG[C/T]GATAATTGTACCAAA	54476
rs374845359	in-del	-/C			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672228	AGAAAACCAAGAATG[-/C]CACCGATTTATTTTC	54476
rs374852971	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5777149	TCCAGCAGTCTTTGA[C/T]AAGGCATGTGAACGA	54476
rs374906084	in-del	-/GGGGTG			intron-variant	RNF216	GRCh38.p7	7:5623944	CACCTGAGGGACAGC[-/GGGGTG]ACCCCCTCCTCTCCT	54476
rs374910601	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5641026	TTTTTTCTTTGGTTA[C/T]CAGTCTATGTAATTT	54476
rs374914168	snp	A/C/G	7.23188e-05	0.0060129	missense, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711775	CCTTTCGGCAGTGAG[A/C/G]ATTAGGACAGCTGAA	54476
rs374925637	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5725214	CACTCCTTGGACTGG[C/T]CTGTCCAGATGCTCA	54476
rs374932674	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5695936	GAAAACATGTTTCCC[A/G]TCAGAACGCATCCAA	54476
rs374954951	snp	G/T	3.32878e-05	0.00407956	missense, intron-variant	RNF216	GRCh38.p7	7:5741791	GTTTGATGAGATTGG[G/T]TCGTGATCTCTGAGG	54476
rs374985580	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5770166	AGCGAAACCCCATCA[A/G]ACAAGATTACTTGGG	54476
rs374994537	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5707854	CCTCAGCCTCCCAAG[C/T]AGCTGCGATTACAGG	54476
rs374998859	snp	A/G	1.64855e-05	0.00287097	intron-variant	RNF216	GRCh38.p7	7:5652528	GGGGATAAAGGACAG[A/G]CACAAAGACAACTCC	54476
rs375027678	snp	A/G	1.81506e-05	0.00301247	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622845	TTTGTGCTGCTCAAT[A/G]GGGATTCGGGGCCAT	54476
rs375033530	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5635504	CTTACCAGGTTTCTG[C/T]GTTTCCTCATCAATC	54476
rs375036100	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5653763	GAGACAGTGAAGGCT[A/T]GAGGAAGTGAGGCCT	54476
rs375038148	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5776553	TGAGCTAAGATCGGG[C/T]CACTGCACTCTAGCC	54476
rs375050417	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5747747	AGGAGACTCCATCTC[A/C]AAAAAAAAAAAAAAA	54476
rs375051555	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5694681	CTGCCCTGGAGCAGA[A/G]ATGTGTATGGTGGCC	54476
rs375065011	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5775844	ACTGCACTCCTGCCT[A/G]GGTGACAGAGCGAGA	54476
rs375075256	snp	A/C	0.00100118	0.0223515	intron-variant, nc-transcript-variant	RNF216, MIR6874	GRCh38.p7	7:5711860	GTCAGAACAGCAGAA[A/C]TGACATTACTTCAAA	54476
rs375082945	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5653004	ACACAGTAGCACGAG[C/T]TGCTTGGCAGGGCCT	54476
rs375109786	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5644721	TGTTGTCCAGGCTGG[C/T]CTTAAACTCCTGGGC	54476
rs375121377	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670634	TCTCCACCCCTACTG[C/T]TTCATTAGTTTCTTC	54476
rs375136020	snp	C/T	3.29614e-05	0.00405951	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741068	CTTGAGATTCTTGCA[C/T]TGGAAAGGCTGGACC	54476
rs375141078	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5697204	CTCCGCCAATAAGAC[C/T]CCACCACGGCCTGGT	54476
rs375148061	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665967	TCAGGAGATCGAGAC[C/G]ATCCTGGCTAACACG	54476
rs375150577	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5649277	GGCGCCTGTAATCCC[A/G]GCTACTCGGGAGGCT	54476
rs375151531	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5696148	GGAAACACACTGACA[A/T]CCACAGTCCATGTGG	54476
rs375164611	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5640253	GATGTCATTTGCCAG[C/T]GAGAATTTATTATTT	54476
rs375167234	snp	C/T			upstream-variant-2KB	RNF216	GRCh38.p7	7:5783232	CCTTCTGGGCTCAAG[C/T]GATTCTCCTGCCTCA	54476
rs375179866	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5733355	TCCCTAAAAATAAGT[A/T]CACGTGTGAGACTCA	54476
rs375199403	snp	A/C/G	6.95645e-05	0.00589729	intron-variant	RNF216	GRCh38.p7	7:5641122	TTCTATTTTCTCCCT[A/C/G]TAAAGCAATAGGCAG	54476
rs375223869	snp	C/T			intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652206	GGTGCCAGGCATTTA[C/T]ATGTTAGTTTGTCTT	54476
rs375248380	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5747227	AACAGGTCATAGTTT[A/T]AAAATGTCCTAAACC	54476
rs375258710	in-del	-/GATCC			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677482	AAAAATGAAATAAAA[-/GATCC]AAGCCATATCGAAAG	54476
rs375277026	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5740029	AAACCAAAAACAAAA[A/C]AAAAAAAACCCGCCT	54476
rs375277624	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5637489	GAAATAGAGAACACC[C/T]GGTTACCACAGAGGA	54476
rs375306690	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5648905	CACATGTAAAGCTAA[C/T]TTGAGATAATTAGTG	54476
rs375324333	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5689598	GCATAAGAAATGTAG[A/T]TTTAGGGCTGTAATT	54476
rs375352224	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5744891	GCAGCAGAATCACTT[C/G]AACCTGGGAGGCAGA	54476
rs375354409	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5762956	TCCTTTAAAAAGAAG[C/T]ATCATGGTGTTAAAG	54476
rs375382714	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5723817	ACAAACTGAAAAGGA[C/G]AAAAATGGGATCCCT	54476
rs375382980	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5756407	GAAACCATATGGCCC[A/G]CGAGGCTAAAATATT	54476
rs375404695	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5744287	AGTAAATACAGTTGA[A/G]GAGAGAAATTAGTGC	54476
rs375483732	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5659659	GACCTTGCAGCACCC[C/T]CTTTCTAAACTAAGG	54476
rs375493802	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5744569	CAAAGTAGAACAACA[C/G]TCTGTTTTGTTTAAT	54476
rs375516590	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672567	GAATAAAAAGAGGTT[C/T]CCAGAATTCATAAAA	54476
rs375533981	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712222	CGGTGGCTCACGCCT[A/G]TAGTCCCAGCACTTT	54476
rs375552822	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5631942	CCCTTCTCCACGCCA[C/T]GGGAGGCTGGCAAGG	54476
rs375578688	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667994	TGAGCAGGTAACTTC[A/G]CGTTGGTATTTTAGG	54476
rs375583458	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712081	ATAAACACGTCCCAA[C/T]CTTAATGAGAACTCC	54476
rs375584180	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5706216	CACAGCGACACTCCA[C/T]CTCAAAAAAAAAAAA	54476
rs375634424	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5756656	GACAGGGTCGCTCTC[C/T]GTTGCCCAGGCTAGA	54476
rs375637420	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5724434	CAGAAACAAATACTG[G/T]ATGGCTATGTACAAG	54476
rs375639283	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5740173	ACTCTGTCGCCCAGG[C/T]TGGAGTGCAGTGGCA	54476
rs375648774	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5655232	TGCTCTGCTCACCCT[C/G]TACGTCACAGTGCTT	54476
rs375677208	snp	A/G/T	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670294	CCATTTCCTGCACAT[A/G/T]CACTGCTCCCCTGAG	54476
rs375679146	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5743455	CTATTACTTATTTGT[C/T]CTACAAAATACTCTA	54476
rs375686642	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5686302	TGCCACGTGGTTTCT[A/G]TGGGGGCTTCTGACA	54476
rs375701040	snp	A/C			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768363	CACACACACACACAC[A/C]CACACACACACACAC	54476
rs375723514	snp	A/G/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5688840	TTAATAATATGATAC[A/G/T]AATTCCCAAATGATG	54476
rs375761600	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5729273	TCTTTTCATTTAGTC[C/T]GTCACGATGAGCAAA	54476
rs375765416	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5763964	GAGGCCGAGGCAGGC[A/G]GATCACTCGAGGTCA	54476
rs375798979	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5759639	ATTTTTCTTCTTTTT[C/T]TTTTTTTTTTGAGAC	54476
rs375819461	snp	C/T	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5660442	GAATACAGGCGCCCG[C/T]GACCACACCTGGCTA	54476
rs375838375	snp	A/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675485	TACGAAAAATAAATT[A/T]AAAAAAATTAGCTGA	54476
rs375855124	in-del	-/TTCCATCTC			intron-variant	RNF216	GRCh38.p7	7:5760506	GGGCAATGAGTAAAA[-/TTCCATCTC]AAAAAAAGAAAAAAA	54476
rs375885929	snp	A/G	6.64209e-05	0.00576247	intron-variant	RNF216	GRCh38.p7	7:5721202	ACAATGCAAAAGCAT[A/G]CAGACAACTATGTGT	54476
rs375887797	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5726850	GCGACAGAGCGTGAC[A/T]CTGTCTTAAAAAAAA	54476
rs375927503	snp	C/T	1.64958e-05	0.00287187	missense	RNF216	GRCh38.p7	7:5715142	ACTGCGTCAGCTCCT[C/T]GAATGGAAATTCCCC	54476
rs375943565	snp	A/G	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5686159	ATCCAGAAGGCAGAG[A/G]TTGCAGTGAGCCGAG	54476
rs375947906	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5725788	CCAGGAGGCGGAGGT[C/T]GCAGTGAGCCGAGAC	54476
rs376022492	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619577	AGGCTGTGCCAACAG[C/T]GAGGGTAGCAGGGCC	54476
rs376049020	in-del	-/AAGG			intron-variant	RNF216	GRCh38.p7	7:5726939	ATTTGAAACGGAAGG[-/AAGG]GTGTGTGAGGTAAGG	54476
rs376049503	in-del	-/GAAA			intron-variant	RNF216	GRCh38.p7	7:5776964	AAAGAAAGAAAGAAA[-/GAAA]AAGAAAGTGAAAGAA	54476
rs376050608	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5647154	GTTGCCTCTGGCAGT[C/T]TTTGCCAGGTTAATT	54476
rs376065267	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5692417	TCCTTGTTAGTCAGA[C/T]ATACTCTGTGGGAAA	54476
rs376071890	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5749196	CCCTCTGTCATACAG[G/T]CTAGAGTGCAGTGGC	54476
rs376096873	in-del	-/ACAC/ACACACAC			intron-variant	RNF216	GRCh38.p7	7:5698384	CTTAGATTCTTTTAT[-/ACAC/ACACACAC]ACACACACACACACA	54476
rs376119380	snp	C/G			intron-variant, nc-transcript-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662480	TAAGATTTGGTAATG[C/G]CATTGCTTGAGATTA	54476
rs376126209	snp	A/G			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620083	ATTTACAAAAGTCCC[A/G]GTTACATATGATACA	54476
rs376151728	in-del	-/G	0.00636936	0.0560724	intron-variant	RNF216	GRCh38.p7	7:5659402	AGGTATGGGTACAGA[-/G]GGAAGAGCAAGGGTG	54476
rs376155909	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5643674	TGCATTCTTTTGCTG[C/T]GGTAAAATGCACATA	54476
rs376165965	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5639353	AGCTGCTAGCCCACC[A/C/T]CTGGGCTGTTCATCT	54476
rs376169926	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5694793	CTGGGCAGAAATTTT[A/C]CAGCCACTCTCTCAA	54476
rs376175919	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5736065	ACCACTGCACTCTAG[A/C]CTAGGTGACAGAGTG	54476
rs376180548	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673898	CAGAGTCTTGCTCTA[C/T]CGCCCAGGCTGGTGT	54476
rs376181376	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5708125	TGGTATGATTTTGAT[C/G]TTAAATTTGTTAAGA	54476
rs376208079	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665360	AAAGGGCTTCTTTGG[C/G]GAAGATTTCATGTTG	54476
rs376231270	snp	A/C			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681820	GACTACATAAACGGG[A/C]AACACCCAGAAAAGG	54476
rs376245816	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5723509	AAAATTAGCCGGACT[C/T]GGTGGCGGGCACCTG	54476
rs376251541	in-del	-/GAGT			intron-variant	RNF216	GRCh38.p7	7:5756120	CTCGTGATAGTGAGT[-/GAGT]CTTGAGGTGTCCGAT	54476
rs376256798	snp	C/T	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5773798	ATCTTGAACTCCTGA[C/T]TTCAGTGATCTGCCT	54476
rs376378022	snp	A/G	1.69559e-05	0.00291164	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5740997	CACTAGTAGTTCAAC[A/G]AGCTCTTGATCTACC	54476
rs376451333	snp	C/G	0.000153988	0.00877328	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741265	GGCTGCCGTTCCTGA[C/G]GAACGACCTGGTTTG	54476
rs376460734	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5689903	CCAAGATTGCGCCAC[C/T]GCATTCCAGCCTGGG	54476
rs376479573	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671963	TCATTTCAGATTTCT[A/G]GCTCCAAAACTGTAG	54476
rs376516312	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5722672	CAGGATTACAGGCAT[C/G]AGCCACCGCGCCCAG	54476
rs376518117	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5711266	GCTCCCACGTAATAT[A/G]GTCAGTTCTCATGAG	54476
rs376529733	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5653935	CCCTGGAGGCCTGCA[C/T]GCACCAGACCAGGCA	54476
rs376544891	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5761544	TACAATCCCAGCACT[C/T]TGGGAGGCCGAGGCG	54476
rs376603161	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680885	TTGTCCTTTCTGTTC[C/T]GCCTCCAAAATGCAC	54476
rs376607290	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5723114	TTCACTTTTTTTCTA[C/T]AAAATGATAATAATG	54476
rs376616591	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5704799	CCGTCACTGCCTCAG[G/T]TCCCCATATAACATT	54476
rs376626070	snp	G/T	1.64806e-05	0.00287054	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741069	TTGAGATTCTTGCAT[G/T]GGAAAGGCTGGACCT	54476
rs376643128	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673696	GCCTGAGCAACACAG[C/T]ATGACCTTGTCTCTA	54476
rs376643917	snp	C/T	1.64838e-05	0.00287083	synonymous-codon	RNF216	GRCh38.p7	7:5716740	CTGTTCTTCATTCAT[C/T]TGTAGGGCAAGCAAA	54476
rs376646826	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5710381	AAAAACAAAAACAAA[-/C]AACAAAAAACGTCCT	54476
rs376647298	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712427	GTAGTGAGCCAAGAT[C/T]GCACCACTGTACTCC	54476
rs376675404	in-del	-/AA			intron-variant	RNF216	GRCh38.p7	7:5631678	CAACATAAAAAAAAA[-/AA]TGCCATTATTTCTTT	54476
rs376681189	in-del	-/GGAAA	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5773494	ATTTCCCCGCCTTGG[-/GGAAA]TCTCCCAAAGTGCTG	54476
rs376724290	snp	C/T	0.0138799	0.0821421	intron-variant	RNF216	GRCh38.p7	7:5650922	CATTGCCCACTTCAT[C/T]TTCTGAGTACCAAAC	54476
rs376731058	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5684988	TATCAGATTTGAGCA[C/G]TCTTTACACAGCATA	54476
rs376739180	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5740906	TTTTTTTTTGCAATG[-/A]AAAAAAAAAAAAGAA	54476
rs376747905	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5740091	GGCAAATAGTGGCTA[A/C]CAGATGTAACACCTT	54476
rs376749450	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5725091	TGAATTTTCTAACAC[A/C]ACACAAAATTTTCCT	54476
rs376754159	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713743	ACCAAAGAAAACAAA[C/T]GGAAAAAGACGACAT	54476
rs376759297	snp	A/G	4.94303e-05	0.00497119	synonymous-codon	RNF216	GRCh38.p7	7:5761049	GTGAATTACCTCTTC[A/G]TTGTTGTTTCCCTCT	54476
rs376775747	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5633705	GAACTCAGCCTGACA[C/G]AGAAGACTCTGGCTT	54476
rs376802207	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5707549	CAGATTTTTCTATGT[A/G]TAAGATCATGTTATC	54476
rs376878330	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666123	GTGAGTGGAGATCAC[A/G]CCACTGCACTCCAGC	54476
rs376924574	snp	C/G	5.64435e-05	0.00531211	intron-variant	RNF216	GRCh38.p7	7:5739259	CCACCACAAAAAAAG[C/G]ATGGTAGTATACTTA	54476
rs376990169	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662809	GTGTGAACAGGGAGG[A/G]TGCCATCTGACACTG	54476
rs376993042	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5700538	GTGTGTGGTTTCTAG[A/G]AAGAGGGCCACTCCA	54476
rs376996320	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5698098	TATGAGGCTATGGGG[A/G]TTTCATCTGAGAAAC	54476
rs377009286	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5710384	AAACAAAAACAAAAA[A/C]AAAAAACGTCCTCAG	54476
rs377009603	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5752210	AAAAATGAAAGTACA[A/G]TGAAAGAAAAGATGT	54476
rs377039575	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5760664	CAACACCTGCAGTAT[C/T]TCAGAACATAAAGGC	54476
rs377055344	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5688008	GAGGGAAAAACAGCC[A/G]TTTTGACAATTTTCA	54476
rs377062060	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665817	TTTAACAGAATCACC[A/G]AGACTATATCAGCAA	54476
rs377062924	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5727308	TCACCCTTATGACCA[C/G]AAGCTTTCCAGCTGT	54476
rs377065088	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5630095	AAATAGAAGGAAAGA[A/G]GATGAGGAGGAGCCA	54476
rs377065551	snp	C/T	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5646558	ATTAGCTGGGTGTGG[C/T]GGCACACAACTGTAG	54476
rs377067529	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781214	TCGGGCCCGGGGGAG[A/G]GAAGCGCGGTCTCCC	54476
rs377067572	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5698745	CAGAGAAGCTGGAAA[A/G]CACCAGGTCCCTACC	54476
rs377082085	snp	C/T			upstream-variant-2KB	RNF216	GRCh38.p7	7:5783436	AACCCGGCCAGAGGA[C/T]TGTTTGAGCCCAGGA	54476
rs377100931	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5755545	TCAAAGGGAGGATTT[C/G]TAATTGCGCAGATAA	54476
rs377102257	in-del	-/CT	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5638670	GGAGACAGGGTCTTG[-/CT]CTGTCACCCAGGCTA	54476
rs377117965	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5652747	GGCTGTGGCAGGCCA[C/G]GAGTTTGAGACCAGC	54476
rs377133944	snp	A/G	0.000200619	0.0100134	intron-variant	RNF216	GRCh38.p7	7:5725317	CCACCAACACAGTTT[A/G]CATTACCTTGTTCAA	54476
rs377153389	snp	A/G			upstream-variant-2KB	RNF216	GRCh38.p7	7:5782550	AATAGCAAGACCCCA[A/G]CTCTTAAAATAATTG	54476
rs377162857	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674052	TTTTTTTTTTTACGA[C/T]GGAGTCTTGCCTTGT	54476
rs377166747	snp	C/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780627	GGAAAATCGCTTGAA[C/T]CCGGGAGGCAGAGCT	54476
rs377189667	snp	C/G	1.64768e-05	0.00287021	synonymous-codon	RNF216	GRCh38.p7	7:5729438	GTAGAGTACCTTTCG[C/G]GTGATTGCATAGTGT	54476
rs377192550	in-del	-/G			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622350	GTTTTGGATGGGGGG[-/G]ACAGCATCTTGGCCC	54476
rs377221721	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5638364	AACTCAGTGAACAGT[A/G]TTGCAGACAGAACTT	54476
rs377240452	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5702744	TTTTAAAAAGTGAAA[C/T]TTTAAAAAGTGAAAA	54476
rs377241912	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5738241	AAAAATTTTTTTAAA[A/G]TAAGAGACAAGGTCC	54476
rs377251763	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5773432	ATTTTTAGTAGAGAC[A/C]ATGTTTCACCATGTT	54476
rs377252092	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5654775	GGACATACATTTAAA[C/T]GCACTGCTTCCGAGG	54476
rs377277574	snp	G/T	0.0425829	0.139564	intron-variant	RNF216	GRCh38.p7	7:5761158	AAAGGAAGCAAAGAG[G/T]AACAGTAAGAATGAG	54476
rs377284123	snp	A/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712022	TGGCTCTTATCAGGA[A/G]ACATAAGCACCACAT	54476
rs377308433	snp	G/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767347	GGACCTGAGGCAGAA[G/T]CAGCAATTTCAATGG	54476
rs377309484	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5721716	ATCATCGGTTTTTAA[C/T]TTTAGCCATTCTGGT	54476
rs377309844	in-del	-/ACACATACACACACAC			intron-variant	RNF216	GRCh38.p7	7:5698411	CACACACACACACAC[-/ACACATACACACACAC]GCATGCATGCTGGAG	54476
rs377313391	snp	C/G	1.64743e-05	0.00287	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741365	CCTGATCATCTGCTA[C/G]AGCAGCTGACTCTCC	54476
rs377335810	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5657673	CTCAGCCAGGGACCA[C/T]AGGACCGTGGGCTTC	54476
rs377344875	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5730421	TCTTGTTTTGCTTTA[C/G]GAATTTGCTTTGTAG	54476
rs377356710	snp	G/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768680	GTTTTTTTTTTTTTT[G/T]GGACAGAGTCTTGCT	54476
rs377371968	snp	A/T	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5638962	TACTTATAATTTTTT[A/T]AAACTTCCTCTGTCC	54476
rs377403342	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5728317	AGGCACGGTGGCTCA[C/T]GTAGGTAATCCCAGC	54476
rs377420292	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5769837	AGGTCAGGAGTTTGA[C/G]ACCAGCCTGGCCAAC	54476
rs377482457	snp	C/T	6.6759e-05	0.00577711	intron-variant	RNF216	GRCh38.p7	7:5715215	GTCAAGAAACACACA[C/T]GAAATGTCCTGCACT	54476
rs377486255	snp	C/G	8.23608e-05	0.00641667	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741428	CGGATGACTGGTTCT[C/G]AGTTTCCAAAGGATC	54476
rs377491826	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5757120	ATGTTTATTACATTT[A/G]TTGACCATGTTCTTC	54476
rs377494551	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5642444	GTCTGGAACTCCCGA[A/C]CTCAGGTGATCCACC	54476
rs377498743	snp	C/T	1.64757e-05	0.00287012	missense	RNF216	GRCh38.p7	7:5641284	ATCTGGGCACCACAG[C/T]GGCAAGACATGCGGT	54476
rs377507486	snp	A/G	1.80357e-05	0.00300292	intron-variant	RNF216	GRCh38.p7	7:5624133	TCATCTTCCTAAAAC[A/G]CAAGCAATGAGAAGG	54476
rs377548684	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5746593	AGTCAGATGGAAACT[A/G]CAAAGTGATTGGCTA	54476
rs377554033	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5635264	TTGATGACAGATCAA[C/T]GATCACACCCACCCC	54476
rs377554258	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5762035	GCATAATAGAATATA[C/T]GGACAGGGATGGTCA	54476
rs377555172	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671524	AGAAGGACAGAGAGA[A/G]CCGGGCACGGTGGCT	54476
rs377559732	snp	C/T	1.65015e-05	0.00287237	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712710	CGCTCTGCCTGAGAA[C/T]GAACCTGACAAGCTC	54476
rs377563284	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5745565	ACTGAAAAATCACTA[A/C]AGATAATAATGGTAA	54476
rs377567302	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768787	CTGCCTCACCCTCCC[A/G]AGTAACTAAGACTAC	54476
rs377568301	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5744003	TCAATCAAAAATAAC[G/T]AGGCATACAAGAACT	54476
rs377569454	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681628	GTTGTTCTTGCTTAG[A/G]AAGTGTCAAGGACGA	54476
rs377573106	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5659130	GTGGTGCAGAATAAG[A/G]TCTGAGTGACGGTGG	54476
rs377576167	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5630493	AGTGATCTTCTCACC[G/T]TAGGCTCCCCGAGTA	54476
rs377593117	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5724781	CTTTACTGGGTGGAA[C/G]CAACTCAGATAAAAT	54476
rs377594609	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5731132	GGTTAAACTACAAAA[C/T]TGGAAAATTTTAAGA	54476
rs377597829	in-del	-/CACT			intron-variant	RNF216	GRCh38.p7	7:5635279	TGATCACACCCACCC[-/CACT]AACTTCACTTTTTTT	54476
rs377600055	snp	A/G	6.59424e-05	0.00574168	intron-variant	RNF216	GRCh38.p7	7:5721001	ACCAGAATCCCAGAA[A/G]CACACCCCAAGACCA	54476
rs377619684	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5745889	TGATAGATTGAGACT[A/G]TCTTAAAAAAAAAAA	54476
rs377626834	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5715811	CAGTGGCACGATCTT[C/G]GCTCACTGCAACCTC	54476
rs377627761	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681892	CATGAAGACGGGATC[C/T]GTGTAGCCCCTAAGG	54476
rs377640224	multinucleotide-polymorphism	AA/GC			upstream-variant-2KB	RNF216	GRCh38.p7	7:5783420	CAGGAGCGAGCCACT[AA/GC]ACCCGGCCAGAGGAT	54476
rs377645168	snp	C/T	0.000313302	0.0125121	intron-variant	RNF216	GRCh38.p7	7:5624168	ACCTGTAGCTTCATG[C/T]AGTGCTGAGGCCCCG	54476
rs377655683	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5730312	ACTGTTAACTAGTAC[C/T]AGTGGTAGGTATATA	54476
rs377655821	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5704520	ATAAAGTCTAAATGC[A/T]CGTAGCGATTTGCTT	54476
rs377659380	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5685881	GTGAATTCTTTATAT[G/T]TGGAGCACTATAATG	54476
rs377674225	snp	A/G	3.45859e-05	0.00415834	missense, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711819	CTGTCCAACAGAGCC[A/G]GAAAGCTACAGGACG	54476
rs377687460	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5650307	GCTGCCAGGTTTAAA[G/T]AGGACCCAGTGGTGG	54476
rs377690417	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5635100	AGCTAGGGATCCTGG[C/G]CTAGTGACCTACACA	54476
rs377692133	snp	C/T			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622145	GGGCCAGCTTCAGAA[C/T]CATCCAGTGTACCGC	54476
rs377700330	snp	A/C			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620406	CTCTGGGCACTGGCA[A/C]GGCCCCTTGCTGGCT	54476
rs377704911	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5714431	GTCTGGCTAATCTTG[C/T]ATTTTTAGTAGAGAT	54476
rs377706040	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5737629	TAATGGCTCCAACAG[C/T]GTCATTGTACAAATT	54476
rs377706123	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5757660	TATATACAGTATGTA[C/T]AATTCCATTTATATG	54476
rs377707695	snp	A/G	9.74659e-05	0.00698022	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5730793	CTTTGGATAATCTGG[A/G]TTTTCCAGAAGAAAA	54476
rs377755489	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5719143	CCCAACAATTTGGGC[A/G]GCTGAGTTGGGAGGA	54476
rs386709752	multinucleotide-polymorphism	AAT/GAC			utr-variant-3-prime, cds-indel	RNF216	GRCh38.p7	7:5621586	GCGGGCCACTCCGGA[AAT/GAC]TGATGCAGCCCCACC	54476
rs386709753	in-del	ACTATTAA/TGTTCTCCTAC			intron-variant	RNF216	GRCh38.p7	7:5625853	GCAACAGTGGATGAC[ACTATTAA/TGTTCTCCTAC]ATTCTCCTACATTCT	54476
rs386709754	in-del	GAG/TA			intron-variant	RNF216	GRCh38.p7	7:5639885	CTGCCTCAACCTCCT[GAG/TA]TAGCTGGGACTACAG	54476
rs386709755	multinucleotide-polymorphism	CA/TG			intron-variant	RNF216	GRCh38.p7	7:5642606	GGCATCACAGGTGTG[CA/TG]CCACCACATCACCAC	54476
rs386709756	multinucleotide-polymorphism	CAC/GAG			intron-variant	RNF216	GRCh38.p7	7:5643544	GTTATCTGTGCTCAC[CAC/GAG]CAGCCAGTGTGTGGG	54476
rs386709757	multinucleotide-polymorphism	CT/TC			intron-variant	RNF216	GRCh38.p7	7:5645266	TCTTGGATGTATAGA[CT/TC]CTTGTTCTTCATCAG	54476
rs386709758	in-del	CT/GAAGAA			intron-variant	RNF216	GRCh38.p7	7:5650193	TCCTCTATCACTAAG[CT/GAAGAA]GCCCAACATTTGGGA	54476
rs386709759	multinucleotide-polymorphism	CA/TT			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674766	TCTAGGAGGCCGAGG[CA/TT]GGCAGATCACCTGAG	54476
rs386709761	multinucleotide-polymorphism	CC/GG			intron-variant	RNF216	GRCh38.p7	7:5728530	AGTGAGCCGAGATTA[CC/GG]CCACTGCACTCCAGC	54476
rs386709762	multinucleotide-polymorphism	AA/GC			intron-variant	RNF216	GRCh38.p7	7:5734124	AATAGGAAGGTGGAT[AA/GC]CAGGGTGTGGGGCAA	54476
rs386709763	multinucleotide-polymorphism	CA/TG			intron-variant	RNF216	GRCh38.p7	7:5764271	TGTGGTGAAACTATA[CA/TG]GGCTATTGGACAGTA	54476
rs386709764	multinucleotide-polymorphism	CAC/TAG			intron-variant	RNF216	GRCh38.p7	7:5766168	GGTGGCATGTACCTA[CAC/TAG]TTTTAGCTACCCAGG	54476
rs387907368	snp	C/T			missense	RNF216	GRCh38.p7	7:5641285	AACCGCATGTCTTGC[C/T]GCTGTGGTGCCCAGA	54476
rs387907369	snp	A/T			stop-gained	RNF216	GRCh38.p7	7:5715095	GTTCTGCAAAGAGTG[A/T]CTCATCAGATATGCC	54476
rs387907370	in-del	-/GA			frameshift-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741401	ATCCGAAGACTCAGA[-/GA]CAGAGCTGTTATCAA	54476
rs397698515	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5697088	CTATTTATCTTCAAA[-/A]GTCCTGCTTCCTTCT	54476
rs397759660	in-del	-/A	0	0	intron-variant	RNF216	GRCh38.p7	7:5776614	AAAAAAAAAAAAAAA[-/A]GACTATAGGGGAAGG	54476
rs397763936	in-del	-/TG			intron-variant	RNF216	GRCh38.p7	7:5757426	TTGTGTGTGTGTGTG[-/TG]GCTATCTGCATGATG	54476
rs397775035	in-del	-/A	0	0	intron-variant	RNF216	GRCh38.p7	7:5745912	AAAAAAAAAAAAAAA[-/A]GAGCAACGAGAACAC	54476
rs397789464	in-del	-/A	0	0	intron-variant	RNF216	GRCh38.p7	7:5649398	AAGGAAAAAAAAAAA[-/A]GACAGAAAGAAAGGG	54476
rs397816564	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5722380	CATGTTTTTTTTTTT[-/T]GTTTGTTTGTTTGTT	54476
rs397830912	in-del	-/A	0	0	intron-variant	RNF216	GRCh38.p7	7:5626684	TAAAAAAAAAAAAAA[-/A]GGAAGAAAGAAAAAA	54476
rs397841509	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5694439	CATTTGACCTTGAAA[-/A]TCCCTGCTTTCCTCC	54476
rs397888964	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5629471	CTCAGAAAAAAAAAA[-/A]GTGAAGATAACTGAA	54476
rs397889291	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5764660	CTCAAAAAAAAAAAA[-/A]GACTCTTCATAAGAA	54476
rs397890059	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5651667	TTTTCTTTTTTTTTT[-/T]GAGACGGAGTCTCGC	54476
rs397891078	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5654711	AAAAAAAAAAAAAAA[-/A]AGGCTCAATCAATGG	54476
rs397891079	in-del	-/A			upstream-variant-2KB	RNF216	GRCh38.p7	7:5782860	TCAAAAAAAAAAAAA[-/A]TTGCCAAGTACACCT	54476
rs397966487	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5707696	TCTTAGTAAAAAAAA[-/A]GCTTTTCAGTGTGTG	54476
rs398003513	in-del	-/T	0	0	intron-variant	RNF216	GRCh38.p7	7:5628701	TTTTTTTTTTTTTTT[-/T]GTAGAAATGGGGTTT	54476
rs398003514	in-del	-/A	0	0	intron-variant	RNF216	GRCh38.p7	7:5653624	AAAAAAAAAAAAAAA[-/A]GAATTAAAAAAAAAT	54476
rs398003515	in-del	-/T	0	0	intron-variant	RNF216	GRCh38.p7	7:5684120	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCGC	54476
rs398003517	in-del	-/A	0	0	intron-variant	RNF216	GRCh38.p7	7:5740012	GTCTCAAAAAAAAAA[-/A]CAAACCAAAAACAAA	54476
rs398003518	in-del	-/T	0	0	intron-variant	RNF216	GRCh38.p7	7:5749168	TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTCCC	54476
rs398003519	in-del	-/T	0	0	intron-variant	RNF216	GRCh38.p7	7:5750937	ATGGCGCTTCTTGCT[-/T]GCACACAGATAAAAC	54476
rs398003521	in-del	-/T	0	0	intron-variant	RNF216	GRCh38.p7	7:5769138	TTTTTTTTTTTTTTT[-/T]GACGGAGTTCCCCTC	54476
rs398047576	in-del	-/TG	0.5	0	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754121	TTTTCTTTTGTGTGG[-/TG]TGTGTGTGTGTGTGT	54476
rs527238870	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677684	TGAGAGTAGGTGAAT[C/T]CCCTTCCAGTCCTGG	54476
rs527244120	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678280	TCCCATTTTACTGCC[A/G]TCTACAAGACTTTCA	54476
rs527253030	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5684489	AGTTTGTCAGCCCTG[A/G]CCTATTCCAGGAAGC	54476
rs527257848	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5716512	AACAGGAACATCTAT[C/T]ATCTTCCCTTCAATT	54476
rs527266025	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5745300	TCACTTCTAAAAAAA[C/T]TTTTTTAAGTCAAAG	54476
rs527267351	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5779113	ATGAATTATGTCTCT[A/G]AAGAGCTAGAATATA	54476
rs527305185	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672639	TTGCTGGTACCCGAC[A/G]ATAAAGACTCATCGC	54476
rs527313120	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678696	TGCCTCCTGGGCCTG[C/T]TACCCTCCAAGCACG	54476
rs527326122	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5641703	AGCATTTAGAAAAGG[A/T]CTGCTCTATTTGTTA	54476
rs527379220	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5774925	CAGCTAATTTTATAT[G/T]TTTAGTAGAGATGAG	54476
rs527389487	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5625553	AACGGACAGTTTGCA[G/T]GTTTACTTACTAGGT	54476
rs527398633	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712567	AAATAAAAATAAATA[A/C]GTAAAATTATTGATA	54476
rs527401370	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5706869	CATGAAGCTTTCCAC[C/T]TACGTTTTCTTCTAG	54476
rs527430873	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673083	GGGGCCTATGTGCAC[A/G]GTGTGGGCATTCCCA	54476
rs527455949	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620813	CTCTTGCTGGAGCCA[C/T]GTGCCTAGGGTACAG	54476
rs527461100	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5694333	TGCTACTCAATGATA[C/T]TCTCTTTAAGGAATG	54476
rs527463914	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5759695	GGAGTGCAGTGGCAC[A/G]ATCTCAGCTCACTAC	54476
rs527471011	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5730912	AATATAGTCCTTAGT[C/G]ACACATTACAACTGG	54476
rs527471102	snp	C/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5725647	TTGAGGTCAGGAGTT[C/G]GACACCAGTCTGGCC	54476
rs527472347	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780491	CACCTGAGGTCAGAC[A/G]TTAGAGACCAGCCTG	54476
rs527473655	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5661747	GGCAGAGGTTGCAGT[A/G]AGCTGAGATTGTGCC	54476
rs527502124	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5621162	AAGGCAGAAAGAATG[A/G]GTATCTTAGTTTTTT	54476
rs527528462	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5636364	TTTGGCTTCATTTTG[A/T]TAACTAACAGAGAAA	54476
rs527536208	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656587	GAGCATGCATGCTGG[A/G]TAGTTTGTTAACAAG	54476
rs527539429	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5651775	TGCCTCAGCCTCCCG[A/C]GTAGCTGGGATTACA	54476
rs527544632	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5779597	GTAATTCTTGTGCTT[C/T]GGGAGGCTGAGGGTC	54476
rs527546094	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5721791	AGCATTCAAATATAC[A/G]AGGGGCTGAAGGAAC	54476
rs527550533	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5650841	CACATGGGCCTCAGC[C/T]GCCTCATCTGTAAGA	54476
rs527550681	snp	G/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754819	GATCACTTGAGGCCA[G/T]GAGTTCGAGACGAGC	54476
rs527584783	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750341	TTTTTAAAGACCAAT[C/T]TGAGATTCCTCATCA	54476
rs527600198	in-del	-/AAG			intron-variant	RNF216	GRCh38.p7	7:5747774	AAAAAAAAAAAAAAA[-/AAG]GGGAAAAAAAAAGAA	54476
rs527628290	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5684065	CTGGTCTGTGATGGT[A/G]GGACCAGTGTTTCCA	54476
rs527635675	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5739152	GTGATAGTTGCATAA[A/T]AATGTGAATTTACTT	54476
rs527643161	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5630302	CCTGGCTTGAGTGCA[C/T]ATGCAGCTCTACCCC	54476
rs527643880	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5635644	AGGGAGATGCTGCGC[C/T]GGCCTGAGGGGAGAA	54476
rs527675162	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671754	AGGTTGCAGTGAGCC[A/G]AGATTGTGCCACTGC	54476
rs527687402	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666642	ACGGGGAGCTCTCAA[A/G]CCTTCTGAGCTGCGC	54476
rs527689643	snp	C/G	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5629711	AGGCGTCTGTAATCT[C/G]AACTACTCGGGAGGC	54476
rs527700541	snp	G/T	0.0185938	0.0946107	intron-variant	RNF216	GRCh38.p7	7:5769170	GTTGCCAGACTGGAG[G/T]GCAGTGGCACAATCT	54476
rs527717152	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5705824	GGGCAGGAGAATTGC[C/T]TGAACCTGGGAGGCG	54476
rs527727932	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674399	CCTGACCTCATGATC[C/T]GCCTGCCTCAGCCTC	54476
rs527747871	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5766866	CAACTATAAAGGGTG[C/T]GTGTGTATGTTTAGA	54476
rs527786181	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5700116	CCACGGGGACAGGGG[G/T]TGTTTTCATGCTTGC	54476
rs527808049	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5735444	TTGGTTAAAGAAATT[A/T]AAAAAAGATTAAAAA	54476
rs527819871	snp	C/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5759195	CTGTCATGATTGTAA[C/G]TTTCCTAAGGCCTCC	54476
rs527823635	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5625371	TTATTTTCCTAGACA[C/T]GGCGTCAGAGCCTAA	54476
rs527846483	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5661192	TGATCTGCCCACCTC[A/G]GCCTCCCAAAGTGCT	54476
rs527848169	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682402	TGACAGTTTTACTTT[C/G]ATTTTTTTTCTTTTT	54476
rs527860628	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5720980	CTAACTAAACCCTAA[A/G]AGCAAACCAGAATCC	54476
rs527862713	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5783255	CTGCCTCAGCCTCCT[A/G]AGTAGCTGGGATTAC	54476
rs527868301	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5749076	TGCCTTTTAGTTCAC[A/G]TGACTTAGGTATTTT	54476
rs527908765	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5743850	ACCTCCCAGGAACTG[A/G]ATCGCAGCGTGGAGA	54476
rs527909224	in-del	-/C	0.0248432	0.108648	intron-variant	RNF216	GRCh38.p7	7:5736276	GTGCGCGCCGCCACG[-/C]CTGACTGGTTTTCGT	54476
rs527930065	snp	G/T	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5715924	TTTTTTGTATTTTTA[G/T]TAGAGACGGGGTTTC	54476
rs527962771	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5646395	AAACAAAACAAAACA[A/G]AAGGAAAAAAAAAGG	54476
rs527963814	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5707826	CCTCCCTGGTTCAAG[C/T]GATTCTCTCCTGCCT	54476
rs527970297	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5640156	GCCCACCTTGGCCTT[C/T]AAAAGTGCTGGCATC	54476
rs527978440	in-del	-/A	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5723459	GAGACCATCCTGGCT[-/A]ACATGGTGAAACCCC	54476
rs527983355	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5635657	GCTGGCCTGAGGGGA[A/G]AAGGCAGGCCTGGGA	54476
rs527988818	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5778550	ACTTGATCCCAAAGC[C/T]CCAGGACATAGCATA	54476
rs527993576	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5744643	AAGACTCTACAAAAC[A/G]AACAAACAAACAAAA	54476
rs527997296	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5640770	TTTAAAATCTAGATT[A/G]TAAGTGAGTCTCATA	54476
rs528009621	snp	A/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5705378	CCTGTGAGACCTCTG[A/G]CTTTCTCCCCACCTT	54476
rs528013541	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671499	GCTATTCCAATCTGA[C/T]AGCCTTATAAGAAGG	54476
rs528021726	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5727188	CCCAGTGTGGCGGTG[C/T]TGAGAAGGTGATCTC	54476
rs528022914	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5773343	CACCTCCTGGGTTCA[A/T]GCGATTCTTCTGCCT	54476
rs528046429	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5691677	GTGAAGTAGAATCTT[C/G]TATCTGGCATGGACA	54476
rs528051162	in-del	-/AAA			intron-variant	RNF216	GRCh38.p7	7:5738115	AAAAAAAAAAAAAAA[-/AAA]TTACAATTATTTCAC	54476
rs528055841	snp	G/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5758296	TATGGCTACAATCAC[G/T]ACCAAGTTAGAATAC	54476
rs528058592	snp	C/G	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5624279	GCACACCGTTCCTTC[C/G]TATTTCCCCGAAGGC	54476
rs528067393	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5660067	GCAAGCAATTCTCCC[A/G]CCTCTATCTTCCGAG	54476
rs528074259	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5763581	GTTGTAGTCTTTTTT[A/C]TTTCTTTTTGAGCCA	54476
rs528075723	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5724797	CAACTCAGATAAAAT[A/C]TGAGTTGTTATAACA	54476
rs528077574	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5729934	GAATCTATGGGGAGT[C/T]GGAAGATCAAGCAAC	54476
rs528081628	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5757254	TTTTAGATCTGCCAA[C/T]TTTTGCTTTGTATAT	54476
rs528083173	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5624688	CCCCCTCGGACCTTG[C/G]CGTCTCTTCTCCCAA	54476
rs528127951	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5628711	TTTTTTGTAGAAATG[G/T]GGTTTCACCATGTTG	54476
rs528130583	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5650533	TGCTGCTCATTTGGG[G/T]TGTCTGCAGAATTCA	54476
rs528132173	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5655364	GCACTTTGGGAGGCC[G/T]AGGCGGAGGGATCAC	54476
rs528139579	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5720382	CATTTTCTTAATAAC[A/G]TTTTCTCTAGCTTAC	54476
rs528140769	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5725088	ACATGAATTTTCTAA[C/T]ACCACACAAAATTTT	54476
rs528144289	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5755767	TGAACATTCTTGTGC[A/T]AGTCTTTGGTGTACT	54476
rs528155602	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5758686	GTCTTTCTTTTGGCC[A/C]ATTTCTCCCTTTTGG	54476
rs528175992	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5626421	AAAGACTAAAAAAAA[A/G]AAAAAGAAAAAAAGA	54476
rs528180623	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5687425	AAAAAGAAAAAGAAA[A/G]GAAAAGAAAGAAAAG	54476
rs528194593	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753931	ACTCGGGAGGCAGAG[A/G]TTGCAGTGAGCTGAG	54476
rs528247285	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671606	TCAGCAGTTCGAGAC[C/T]AGCCTGACCAACATG	54476
rs528272836	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5737646	TCATTGTACAAATTA[C/G]AAAAAAGTACCTACA	54476
rs528278930	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664872	ACAATCTTGGCTCAC[C/T]GCAACCTCCACCTCC	54476
rs528284757	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670201	GGCCTCCCAAAGTGC[C/T]GGAATTACAGGCGTG	54476
rs528290943	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5690976	CTTATCCAGCACACA[A/G]CCAGGAGAGGCTGAA	54476
rs528295994	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5709816	CTAGAGTGCAGTGGC[A/G]CAATCATGGCTCAGT	54476
rs528296898	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670683	TGACCTTTGGAAGCA[A/G]AAGTACAGCTAAGGT	54476
rs528302252	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5718686	CTCCCAAGTAGCTGG[G/T]ATTACAGGTGTGTGC	54476
rs528310407	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5772483	GCGATCTCGGCTTAC[G/T]GCAACTTCCATCTCC	54476
rs528311713	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5733376	GTGAGACTCAGGAAG[G/T]AGGAGAACAGAACTG	54476
rs528325020	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5738162	AGGAGGGGAAAGAGT[A/G]TATTTTTCATTTTAT	54476
rs528342448	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5659616	TTCTGGCTGCTACTG[C/T]TAAAGGGATGGTTTG	54476
rs528350524	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5716886	CAATTACACAGTTTA[C/G]CAGTTCAAAAAGGTT	54476
rs528358675	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5654776	GACATACATTTAAAC[A/G]CACTGCTTCCGAGGG	54476
rs528365101	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5629224	AAAAGTGAAGACAAT[G/T]CCAGTGCTTTGGGAG	54476
rs528369264	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5634346	GGTCATGTGTGGCCA[A/C]AGCTGTTGTTAATAA	54476
rs528411097	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5733851	GTATTGTCGAAGAGT[G/T]GTTAAAGCAATTCAC	54476
rs528427844	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5778936	TTTAGTAGAGACGGG[A/G]TTTCACCATGTTGGC	54476
rs528436841	snp	A/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5763141	ACAACCCATGTCTAT[A/T]ATGGAAGGAGAAAAG	54476
rs528437184	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680669	GGCCTCCCAAAGTGC[C/T]GGGATTACAGGTGTG	54476
rs528441930	snp	C/G	0.0115144	0.0749975	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781454	CCGCCCCCACCCCCG[C/G]AGCTCCACAGAGGCG	54476
rs528466469	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5723858	AGGGATTCTTAGCCT[A/G]TGTCCTTATAAAAAG	54476
rs528470563	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5752810	CAGATCACCAACTTG[C/T]AATAATGTCTCATTG	54476
rs528472539	in-del	-/CCAT	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667447	AACTGAAAACCAGCC[-/CCAT]CTCTAGTTACCCTGG	54476
rs528474109	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5781896	GAGCCACCATCTCCC[A/C]AGAGCTGAAAAGGGT	54476
rs528499345	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681246	TAATGTAGGAACCTC[C/T]CTACCTCAGGAAATC	54476
rs528504631	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713875	TTATTTCCATTTTAC[A/G]GAGGAAGAAACAGTG	54476
rs528521986	snp	A/C	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5714366	CAGATTCAACCAATT[A/C]TCCTGCCTCAGCCTC	54476
rs528523500	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643943	TCATAGGAATGGAAA[C/T]CACACGTGTGTTTTT	54476
rs528528869	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5719768	AAAATGCCTGCCAAA[C/T]ACCTATTTTGAATAA	54476
rs528531458	snp	G/T			missense	RNF216	GRCh38.p7	7:5652461	GCCAGCTCTTCACAG[G/T]TGAGGCCATTATGTT	54476
rs528541801	snp	A/G	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5649968	ATAGGATAACACACC[A/G]TTCTACTTGAACGAC	54476
rs528560120	snp	G/T	0.0193772	0.0965046	intron-variant	RNF216	GRCh38.p7	7:5638649	TTTTTTTTTTTTTTT[G/T]GGGGGGGAGACAGGG	54476
rs528572047	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5644380	TAGTCATCCTAATAG[A/G]TGTGAAGCGGTATCT	54476
rs528585851	snp	A/C			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673671	TCATCACAGCAAATA[A/C]AAATATTAAGCCTGA	54476
rs528610503	snp	G/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5639084	TCTTCCCGTCTCACT[G/T]GCAGTTGAGGAAGAA	54476
rs528611667	snp	G/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5772151	GGCAGGAGAATCGTT[G/T]GAACCCGGGAGGTGG	54476
rs528642601	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5762022	CTCCAAGAAATACGC[A/G]TAATAGAATATACGG	54476
rs528656193	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5628254	TGTCTTGGGAGTCAC[A/G]CCCTTAGGAGTCTAA	54476
rs528656522	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5732766	GTGGGGAAGCCTGTC[C/G]GACTTCAATCTGCCC	54476
rs528685806	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5727870	GGTATCTCTGGGTAC[A/C]TCATCCTGGCTGGTG	54476
rs528702112	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5739933	GCTTGAACCCAGGAG[A/G]CGGAGGTTGCAGTGA	54476
rs528737623	in-del	-/AAA	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5765069	AAGCAAGACTCTCTT[-/AAA]AAAAAAAAAAAAAGT	54476
rs528738590	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5653894	ATGTTCAGTTCCTAT[A/G]GCTGGACTGCAGACA	54476
rs528743598	snp	A/T	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5756721	TGACCTACTACTGGG[A/T]TCAAGTGACCCTCCC	54476
rs528745208	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5723591	GGCGGAGTTTGCAGT[A/G]AGCCGAGATTGCGCC	54476
rs528747916	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5691470	TCAAGGTTAAAGGCA[A/G]TAATGGAGAGAGCTA	54476
rs528784362	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5752343	TAAAGTAGCCTTGAC[G/T]ATATGAAAAGACAAA	54476
rs528807774	snp	C/G			intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5777523	AAGACACTGACTGCA[C/G]AGTTAGAGTCGATGG	54476
rs528826373	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5757668	GTATGTATAATTCCA[C/T]TTATATGAAATGACA	54476
rs528844410	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5641076	TCAAATTTTGTTACG[A/T]ATATTCAAAATATTT	54476
rs528873968	snp	C/T			upstream-variant-2KB	RNF216	GRCh38.p7	7:5782675	GCCACCATGGTGAAA[C/T]CCCGTCTCTACTAAA	54476
rs528900954	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5771310	AATAAGTTTCTAGAA[G/T]ATAACACAAAATCTC	54476
rs528916975	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736753	TCTGGGATGTGAGGA[A/G]CGCCTCTGCCAGGCT	54476
rs528922646	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5660744	CACCATGCCTGGCTA[A/G]TTTTTTGTAGAGATG	54476
rs528940270	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5696045	CTGTGGCTCTCAGCA[C/T]AACCCAGCACGGCCT	54476
rs528956687	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5696056	AGCACAACCCAGCAC[A/G]GCCTTGATCCCTGAC	54476
rs528969150	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5702180	TGCCTCTGCGAGTTT[C/T]GAGGGGAGAAACCTG	54476
rs528970692	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5692788	CAAGTTCTCTTAATA[C/T]AAACAAAACAAAAAT	54476
rs528986423	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5702761	TTAAAAAGTGAAAAC[G/T]GACAGAAGTACTCAG	54476
rs528997854	snp	G/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682456	TCTGTTGCCCAGGCT[G/T]CAGTGCAGTGGCGCG	54476
rs528998232	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5761659	GGCGTGGTGGCACGT[G/T]CCTGTAATCCCAGCT	54476
rs528998368	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5766561	GGGAGAAGGCAGTTG[C/T]CTGAGATCCAGGAAG	54476
rs529007533	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5737008	CTGCCCGGCCGCCAC[C/T]CCGTCTGGGAGGTGT	54476
rs529013058	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5627850	GGGAGAAGAGCTCTG[A/G]CCCCCTGTGGCACTG	54476
rs529020475	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5732328	TGTGCATATTTGATG[C/T]GGCGACAAACCAGAC	54476
rs529029711	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5685414	CCTGGGATGGAAGCC[A/C]GGGTGTAAGGGAGGA	54476
rs529036458	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5751037	AGTTGGGGCCCTAGC[C/T]GAGGAGCAGCCTCCA	54476
rs529116973	snp	G/T			utr-variant-3-prime	RNF216	GRCh38.p7	7:5621667	CTCTCAGAACCCCAT[G/T]GCAACACGACAAGGA	54476
rs529122133	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5751484	TTCATTTGATCTTCC[C/T]AGAAATTGAAAGAAA	54476
rs529141820	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5718251	CCAGGCATGGTGGGG[C/T]GCACCTGTAATCCCA	54476
rs529144503	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5717732	AGTGACTGCCAGGAT[A/G]CATGGTTAAATGAAA	54476
rs529160710	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5642838	GTGCCCAAACACAAC[C/T]GCAATTTTCTACAGC	54476
rs529170246	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5769076	TCAAAATTTATGTGA[A/C]GGAGGTAAAATAGTT	54476
rs529174777	snp	C/G/T			intron-variant	RNF216	GRCh38.p7	7:5642514	GCCACTGTGCCTGGC[C/G/T]TATTTTTTTTGAGAC	54476
rs529177384	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673747	CTGGGTGCAGTGGTG[C/T]GCACCTGTAATTCCA	54476
rs529184047	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5775583	AGCAAAAAGTGGGCA[A/G]AGCAGGCCAGGTGCA	54476
rs529198853	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780697	GCAACAGAGCAAGAC[G/T]CCGTCTCAAAGAAAA	54476
rs529199921	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5687262	TAAACTGGGCATGGT[A/G]GCGGGCGCCTGTAAT	54476
rs529200290	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5740826	ATGTCTTCAGAGTGT[C/G]TCTTCTATTCTGTAC	54476
rs529241948	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5731358	ATTGAGTTACACGTG[A/G]TTTATTTAGCTAGCT	54476
rs529279572	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5694951	AAGACCCTGGTTAAC[C/G/T]GACATACAAATCCAC	54476
rs529284465	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712149	GATTGTATCTACGGG[C/T]CAGAAGATTTGGGGG	54476
rs529287330	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5657111	TCTCAGAAGCAGAAC[A/G]AAGTACAAACTGCTC	54476
rs529301269	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5652677	TCTTTTAATAGAAGA[A/G]GTTAAGAGGTGGTAG	54476
rs529301278	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5657524	GTGAGCCGAAATCTT[C/G]CCATTGCACTCCAGC	54476
rs529326417	snp	A/G	4.94352e-05	0.00497143	intron-variant	RNF216	GRCh38.p7	7:5760960	TGTGATACTAAAAGA[A/G]AAAGCCACAGGGAAA	54476
rs529347895	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5755465	ACCACCACAAGGTCA[A/C/G]GAAATATTTCTAGCA	54476
rs529356108	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5722444	GCCCAGGCAAGGGTG[C/G]AGTGGTGCGATCTCG	54476
rs529361055	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621524	CGAATGACGGTGCCC[A/G]CCTGCCCCAGGCACC	54476
rs529361553	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5653319	TAAAGAGCCAGGCGC[A/G]GTGGCTCACACCTGT	54476
rs529365491	snp	A/G	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5779502	AGCCGACTAAATTGA[A/G]ATGTTTCATAGAATC	54476
rs529382984	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5689937	CTCTGTCTCAAACAA[A/C]AAAAAAAAAAGAACA	54476
rs529393232	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5695347	CCACAGAGACGAAAA[C/T]GACACGCCAGCCTGT	54476
rs529398845	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5647646	TCCTATACTTAATCT[C/G]TCCCACTCCTGGTTC	54476
rs529413452	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5756051	ATCCCCACAAGTCAC[G/T]AGCGGGACAGGTGGA	54476
rs529417944	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622038	AAAAGCTGCTCATCA[C/T]CCAGGGTGGCAGAAA	54476
rs529433249	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5779536	CCGCTTCTCTCCCTT[A/C]TCAGCGCGTAAAGAA	54476
rs529450428	snp	C/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753670	TCCTGTCTAGTTCCA[C/T]GGGAATATCAAAGGT	54476
rs529468768	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5774811	TTGCCCAGGCTGGAG[C/T]GCAATGGTGCAATCT	54476
rs529469744	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668752	AACGCTGTTAGGAAG[C/T]AGCCGGGGTCTGCTG	54476
rs529479964	snp	C/G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5735601	GGGCTAAAAGAACAC[C/G/T]CCTGAAGAAATCATC	54476
rs529487578	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5739748	GCTCATGCCTATAAT[C/G]GAAGCACTTTGGGAG	54476
rs529496560	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5740231	TCCTGGGTTCACACC[A/G]TTCTCCTGCCTCAGC	54476
rs529501064	in-del	-/AT	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668177	CTGGTAGTTTTTCAC[-/AT]TCTCATAAAAATCAA	54476
rs529516522	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672986	CAGCTCAGGATCTGC[A/G]GTTTATAGATGTATT	54476
rs529517279	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5706313	GGTCTGTTAGCAAAA[C/T]GTTGTACAGCTGATC	54476
rs529529512	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5769812	GAGGCCAAGATAGAC[A/G]GATCACTTGAGGTCA	54476
rs529540982	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5631596	ACTTGAATCCCATGG[A/G]GGTCCCATGACATTT	54476
rs529543067	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666039	GGCGTGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT	54476
rs529551584	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669630	AGGTGCAGTGGTTCA[C/T]GCCTGTAATCCCAGC	54476
rs529558864	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5632022	CACCAAGGTGGGCAG[C/T]GTGCTGAGGCCAGGG	54476
rs529559259	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5661852	GAAGGCTCAGAGGGT[C/T]CAATTAATTTGGTCG	54476
rs529564906	snp	A/C	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5735931	GAAACTGTCTCTACT[A/C]AAAACACAAAAATTA	54476
rs529572075	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5700943	TCTAGTATAGCGTAT[C/T]GCCGTCTTTGTTTCT	54476
rs529580452	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5700233	TATCACTTTCCACCT[C/T]AGCACACACCACAAG	54476
rs529587217	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664740	TCCTCTGCACTCCCA[A/G]AAACAAGATAATCCA	54476
rs529606205	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5770531	ATACCATATTCACGG[C/G]TGGGAAAGTTCAATT	54476
rs529612422	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5689144	TATGCAGAACCAAAA[C/G]CACAGGAGGGAGGTG	54476
rs529637704	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5705586	ATCCCTCTTGGCAGA[C/G]GGAAAAAATGAACCA	54476
rs529645166	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5683401	CCAACTCTATTTTCC[G/T]GCAACAGTGCCCAGA	54476
rs529646005	snp	A/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5765121	TTTTACACATTCAAA[A/G]ACTAAGAGAGTTTAC	54476
rs529649543	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5660265	GCCCTGTTTTAAATT[-/C]TTTTTTTTTTTTTTT	54476
rs529674355	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5719560	CAGAGATGGGACAAT[C/G]TGAATATCACCAAGA	54476
rs529683554	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5716069	TATTTATTTTTAATT[A/T]TTATTAGAAATGGGG	54476
rs529695096	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754710	CCCAAGAAAAAGACA[C/G]ACAATCTTGGTGTAC	54476
rs529697498	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5721743	TGGTGGGTGCAAATG[G/T]GCTGTATGATTTTCA	54476
rs529723869	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5775750	TGCAGGCACCTGTAG[C/T]CCCAGCTACTCGGGA	54476
rs529726248	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677618	GTGTTAGCATCCTCA[G/T]ATTGGAAAGAACTGA	54476
rs529740706	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5651742	CAACCTCCGCCTCCC[A/G]GGTTCAACTAATTAT	54476
rs529755085	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711529	TCCTAAAGAAGATGA[C/T]ATAAAATAGGAATCC	54476
rs529782089	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5739672	TACAATCTCATGCCA[G/T]CCCTCAAGCAGCACA	54476
rs529784084	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5640991	CAGCATGAGGAGTAG[C/G]TGATAATTAGTTTCT	54476
rs529788918	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750272	ACCTCCAGATGCTGG[A/T]TACAGCACACAAAGA	54476
rs529797754	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5738146	ACCTCTGCAGATTAG[A/G]AGGAGGGGAAAGAGT	54476
rs529812358	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5699544	AACACTAGCTTTTTG[C/T]TGTGTTCTTCACCCA	54476
rs529826468	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666615	AGAACCCCACCTGCA[A/G]GGATCCCTTTCACGG	54476
rs529829078	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5774207	CCATTTAGTCAATCG[A/G]TGGCTCCAGATAAAT	54476
rs529841215	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678206	GGGCCCTCTGCTGAC[C/T]GCCTGCTGTAACTTT	54476
rs529851702	snp	A/C	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5624883	CATGCAGCTCCCACA[A/C]CCCCACCTGCCAGCA	54476
rs529861308	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5759418	GAAGACCTTTAGAAT[C/G]GTCCACTTCCACTTA	54476
rs529873407	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5660686	TGGCTCAAGCGATCC[G/T]CCCACCTCAGCCTCC	54476
rs529874396	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5654380	TTCTGGTGGGATGTC[A/G]TAAAAAGCCTCAATC	54476
rs529874656	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677234	CAGCACGTGCTTCTG[C/T]AACATCAGCCAAGGA	54476
rs529888477	snp	C/T	0.00795532	0.062565	intron-variant	RNF216	GRCh38.p7	7:5661185	CCTCAAGTGATCTGC[C/T]CACCTCGGCCTCCCA	54476
rs529906513	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5730134	CATCAAAAGAAAAAA[C/G]ATATTCCACTCTGGG	54476
rs529920407	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5763922	GGCAGGGCACGACAG[C/T]TCATGGCTGTAATCT	54476
rs529926878	snp	C/G	1.6473e-05	0.00286988	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741410	GCTCTGTCTCTGAGT[C/G]TTCGGATGACTGGTT	54476
rs529939471	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5625336	GTCCCAACAATGCAA[A/G]CAGTCTAATGAAAGC	54476
rs529940878	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5687067	CACAGTCAAGTGAAT[A/G]TTATAGAAACACCAG	54476
rs529956919	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5759161	GCCATGTGAGACAAG[C/T]GTGCTTCCCCTTTTC	54476
rs529967125	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656186	AGACAGGAGAATTGC[C/T]TGAACCCAGGAGGTG	54476
rs529967985	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5725589	GGTGCGGTGGCTGAC[A/G]CCTGTAATCCCAACA	54476
rs529968342	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620707	AGGAGAAACATCACT[C/G]TGGGCTCCCCCTCCC	54476
rs529986685	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5649517	CTGTCTCAAGGCGAG[-/A]AAAAAAACGTTTTGA	54476
rs530040705	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5765447	CCAGCCTAGGCAACA[C/G]GGTGAGACTCCATCT	54476
rs530041010	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5772904	CTGCCTCACCCTCCC[A/G]AGTAGCTGGGATTAC	54476
rs530062131	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754412	AGTGCTCCTCCCACC[C/T]CGGCCTCCCAAGAAG	54476
rs530073894	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5778068	TCCATCCCTTGACAT[C/G]TTTTCATACGGCATT	54476
rs530100866	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5764107	GAGGCAGGAGAATTG[C/T]TTCAACCAGGGAGGC	54476
rs530129148	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768784	CTCCTGCCTCACCCT[A/C]CCGAGTAACTAAGAC	54476
rs530142311	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5738657	AGCTTGCAGTGAGCC[A/G]AGATCGCACCACTGG	54476
rs530145692	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5698777	CTTATATAGAAGAAT[C/G]TTGTGCAGAGAAACT	54476
rs530148351	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5705706	CTGAGGTCAGGAGTT[C/T]GAGACCAGACGGACC	54476
rs530156124	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5739132	AGTTCTGAAGATGGA[C/T]GGTGGTGATAGTTGC	54476
rs530157340	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5634485	CCCTTGCTGTCCCCA[A/G]CAACAGGAAGTTGGG	54476
rs530173601	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666032	TTAGCCGGGCGTGGT[G/T]GCGGGCGCCTGTAGT	54476
rs530213695	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5635869	CCAAATGGCTAGGCG[A/G]TAATTGTACCAAATT	54476
rs530219012	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5655303	CTTACTGAAGGGCCC[A/G]AGGGTCCCGGAGAAC	54476
rs530235632	snp	C/G	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5701940	CTGGTCTCCTGAGAA[C/G]GTGGAAACACTAACC	54476
rs530239010	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5734457	GTTTGGTTTGTGATA[A/C]ATTATTGAGCTGTGC	54476
rs530240793	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5779563	AGAATGTTCTGGCAG[A/G]GCACGGTGGCTAAAG	54476
rs530272663	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782604	CCTGTAATCCCAGCA[A/C]ATTGGGAGGCCGAGG	54476
rs530282324	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619879	TCACCTGATCTTCCT[C/T]CCTGGCAGGGGAGTG	54476
rs530299770	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5748727	AGTAGTTAAGTAGTT[A/C]TTAAGTAGTACTAAG	54476
rs530328670	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5645828	CTCCTGACCTCAAGT[C/G]ATCCGCCCACGTCAG	54476
rs530334683	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5743175	CTGACGGAGCAGAAT[C/T]GCTTGAACCAGGGAG	54476
rs530335026	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5749048	TTATCAGAAAAACAG[G/T]ACCTAACTCCAATGC	54476
rs530340398	snp	A/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5704300	CCAACTGGAATTTAT[A/G]TTACTGGCAAAGACA	54476
rs530348563	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5709940	TTAAAATTTTTTTTG[G/T]AGAGATAGGGTCTAT	54476
rs530354791	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682327	CCCTCTAAAAGGGCA[C/G]CCATGGAGCACATGT	54476
rs530357009	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676040	TTTTTTTTGAGACAG[A/T]GTCTTGCTCTGTTGC	54476
rs530364143	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5720300	CAACGTGAAGACCAT[A/C/G]AAGATAAAGACCTTC	54476
rs530365552	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5746511	AACTCAGGCTTTTGG[A/C]ATCTGTGGGTATGTG	54476
rs530368055	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5650402	TGAAGGCTGTGCTTT[G/T]TAAGTAATTCTCCTT	54476
rs530371611	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678266	AGTCTGAAAAATCTT[C/T]CCATTTTACTGCCAT	54476
rs530376586	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5714894	TCTGCTGTGCTCAGA[A/G]AACCCACATAATCAC	54476
rs530382163	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5645146	GATTAGGCTGTTCTC[C/T]TACTGCTTTCAAGAT	54476
rs530383515	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5733279	TTTCACGAGAATTTT[A/T]ATGTGTTTAAGGATC	54476
rs530398533	snp	A/G	0.00914312	0.0669923	upstream-variant-2KB	RNF216	GRCh38.p7	7:5783185	GCCAGGCTGGAGTGC[A/G]GTGGCACGATCTTGG	54476
rs530419285	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768158	GTCCAGACTTTGATT[A/T]AAAAAAAAATTACCA	54476
rs530430658	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5729098	CTGAGCCACCTGGGG[A/G]ATGGATGGTCGTGTG	54476
rs530444599	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5762628	ACCCGGGAGGCAGAG[G/T]TTGCAGTGAGCCGAG	54476
rs530480953	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5629073	GTGTGGTGGCGTGTG[C/T]CTGTAATCCCAGCTA	54476
rs530493156	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5771381	AAACAGTACTATCCA[C/T]AAAAGAAAAAACTGA	54476
rs530495220	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5660012	CAGGCTGGAGTGCAG[C/T]GGTGCCATTATAGCT	54476
rs530498917	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5625895	GCCTCAGATGCCAAG[G/T]GATGGGTTTGGACTA	54476
rs530502490	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664720	TCCCCCACTGGCCAG[C/G]ATTCTCCTCTGCACT	54476
rs530506016	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5777910	CTGTCCAATGAAAAT[C/T]AGTTTAGAAACTAGG	54476
rs530525095	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5644761	CTGCCCGACCTTGGC[C/G]TCTCAAAGTGTTGGG	54476
rs530545426	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5624232	CCATGGAACAAGCCC[A/G]AAGCCTGCTGCTGGC	54476
rs530598192	snp	A/G	1.65124e-05	0.00287331	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5729567	AAGAGGGGTCAATTT[A/G]GAATAGTCAAAAAAG	54476
rs530615579	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5741964	ACATTTATCTTAACA[C/T]TGAAATTTGATTACA	54476
rs530617181	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5763700	CTCAGCCTCAGAGTA[A/G]CTGGGACCACAGGCA	54476
rs530650328	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5737095	AAAGGGGGAAATGTG[G/T]GGAAAAGATAGAGAA	54476
rs530651561	snp	C/T	0.000798403	0.0199641	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619613	ACTGCAGTGTCTCAC[C/T]AGTCAGGGAAGGGAC	54476
rs530656381	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5638537	TCTGAAAACTACCTA[C/T]CAGCAGCCAGGTACT	54476
rs530679974	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5758151	GTTCTTAAAGAAACT[C/G]TTCAAGTATATTTAA	54476
rs530681340	snp	C/G	0	0	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664200	GTATCTATCTCCTCT[C/G]TGAAAGAACATTATT	54476
rs530683651	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5689202	GGGTCTGGGGAGGTG[A/G]ATGCTTGACGGGGGC	54476
rs530685624	snp	C/G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5716338	AACATGGTGAAACCC[C/G/T]GTCTCTACTAAAAAT	54476
rs530692265	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5638978	AAACTTCCTCTGTCC[A/G]TTTTTGAGTTGAGGT	54476
rs530692620	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5633520	GTTCAGGCTGCAGTG[A/G]GCCGAGATCACATCA	54476
rs530699417	snp	A/G/T	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5781839	TCCCCCACGAGGCAG[A/G/T]AGGGTGAAAGGAAAG	54476
rs530702333	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5733048	GGCCATTTAAAGATG[C/T]ACATAAAGCAACTGA	54476
rs530727428	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5633830	ACTTGAAGACGGCAA[A/G]TGAGGTAGAATTTAC	54476
rs530733343	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5737570	AAATATAAATCTGAT[A/G]ACAGTGGTTGCCTCT	54476
rs530756556	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5763612	GTCTCTCTCTGTCAT[C/T]CTGGCTGGAGAGCAG	54476
rs530758580	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5734869	AAATAAATAAATAAA[A/T]GGTTTGCAGGGCATG	54476
rs530766903	snp	C/T	0	0	intron-variant	RNF216	GRCh38.p7	7:5742353	AACCCAGCCCTGAAT[C/T]ATAATTTAACCTGAG	54476
rs530797842	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670082	CAGGCACGCACCACC[A/G]TGCCCAGCTATTTAT	54476
rs530798498	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5653833	AAACAGATCAACACT[C/T]CAGACAATGGGCAGC	54476
rs530817084	snp	A/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5772044	TTCGAGACCAGCCTG[A/T]CCAACATGGAGAAAC	54476
rs530825798	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5702943	TAGGGCTGCTGTGGG[A/G]ACCAATATGAGCTGA	54476
rs530836562	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5649100	AAGAAAGTGACGGCC[A/G]GGCGGGCGCGGTGGC	54476
rs530875475	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643514	ATGCAGCCAGCGACA[A/G]CCCAGACTCCTGTAG	54476
rs530889641	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5691428	AAGAGCAGGAACAGA[A/T]GAATGCGTAAGTGTA	54476
rs530890598	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781290	ACTTCGCGAAGTGGC[C/G]AGAGGGGGCCACCCG	54476
rs530913368	snp	C/T	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5751653	TTCTGTCTCCCTGTC[C/T]CAGCCTGACAAGAAA	54476
rs530914927	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643892	CTACAGATTGCCATT[A/C]TGAGGCTAGGCAAAT	54476
rs530916785	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5747451	CAGTCTACTTATGGG[C/G]CAGGCAAAGCCTGAA	54476
rs530946419	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5680180	CAGAGCTCGCCCTGG[A/G]AACACACGCTCCCCT	54476
rs530974802	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5654164	GAAGGCCCAGACAAG[A/G]GTGGTGGGCAAGGAC	54476
rs530980559	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5702125	TGGCTCTGAAATGCA[A/G]GTGGGTGTGGGCTCT	54476
rs530980625	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5695512	GCGCCTACTGCTGAG[A/C]GTGCCTCTCCCTGCC	54476
rs531024217	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5690756	TCTGCTGATGCTCCT[G/T]CAATACAGCCCACAC	54476
rs531034880	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5765906	TGCAGTGAGCCCAGA[C/T]TGCACCACTGCAGTC	54476
rs531051612	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5631526	ATCTCAAAGGCAGAA[A/G]CGAATGCTTCAAGAT	54476
rs531054804	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680605	GACGGGGTTTCACCA[C/T]GTTGGCCAGGATGGT	54476
rs531071609	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5761556	ACTTTGGGAGGCCGA[A/G]GCGGGCAGGTCATGA	54476
rs531081757	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5727710	CTCCAGCCTGGGTGA[C/G]AGAGAGAGACCCTGT	54476
rs531086671	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5696869	GCAAGGTGTTCCAAT[G/T]CCCTTGATATTCTAT	54476
rs531096581	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5705190	GATCTAGGGTCACTG[A/G]TTTATGGAGCACCTA	54476
rs531098680	snp	A/G	0.00199481	0.0315187	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622142	AATGGGCCAGCTTCA[A/G]AACCATCCAGTGTAC	54476
rs531128178	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5731983	TGACATCTCAATGCA[C/T]TTCCCTTTGCCGTTA	54476
rs531134005	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622742	TGGGAAGAAAACCAG[C/T]CTACCCTTCAAGCTG	54476
rs531151141	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5690922	TTGGGGGCTGAAGAC[A/T]ACCTACAGATGAGTC	54476
rs531158541	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5723797	GAGCAGTGTTTAGAC[A/G]GAAAACAAACTGAAA	54476
rs531166750	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679222	GTGGCGGGGGGGCGG[C/T]GCACACAGCTAACAA	54476
rs531172271	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5732265	AATTAGCCACCAGCA[A/G]AAATCGCGTCTGTAG	54476
rs531173095	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5780193	TTCCTGGCAATTCCG[C/T]TACTAATTCATGGGT	54476
rs531200619	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5746423	GTGGGTGCAACTCCA[C/T]TTGCTGCTAGCATAC	54476
rs531201684	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5776194	AACAAGAATTGGTTA[C/T]GCATCATCGGGAATA	54476
rs531205790	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5657999	CTGAGAGAGTTACAT[A/G]TCGGGGCAAATCAAG	54476
rs531239928	snp	A/G			intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652269	GAAACAGAGGCTCAA[A/G]GGTTAGATTACTTCC	54476
rs531296111	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5775852	CCTGCCTGGGTGACA[A/G]AGCGAGATTCCATCT	54476
rs531309588	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5632068	TGTAGGTTCCAAGGA[C/T]GGCCGGCAGTTCTCA	54476
rs531361327	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5689872	TTGAATCCAGGAGGC[A/G]GGGGGTTGCAGTGAG	54476
rs531376190	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5642639	CCTGGCTTTCATGCC[C/T]GGCCATTTTTTGTAT	54476
rs531387681	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5755428	TCTATGAATTAATAC[A/G]AAGGGCCATCTGTGT	54476
rs531387901	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5657059	TGTCCGTCCCCATGC[A/G]TGCTAGATTTCAGTT	54476
rs531389131	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5726584	CAAATCAGGGTGGGC[A/G]CGGTGGCTCACGCCT	54476
rs531414828	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5637551	CAGGATTATACATTT[C/G]TTTCCCTTTTTTTGA	54476
rs531428993	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5703487	GGAGGCTGCAGATGC[C/G]TGTTTTTTAACCAAC	54476
rs531443158	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5707803	ATCTCTGCTCACCGC[A/C]ACCTCCACCTCCCTG	54476
rs531469653	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5765535	CTCAGGAAGCTGAAG[C/G]AGGAGGACTGCTTGA	54476
rs531472446	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5647588	ATCCTTCCGCCTTGG[C/T]CTCCCAAAGTGCTGG	54476
rs531508015	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5638573	CATTTCCATTTATTT[A/G]ATTATTAGGGGTGGC	54476
rs531513878	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5660635	CAGGTTGGAGTGTAG[C/T]GGCACAATCTTGGCT	54476
rs531593249	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5717141	GGCAGATCACCTGAG[A/G]TCAGGAGTTCGAGAC	54476
rs531593504	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5722714	TTTTTAAATTCAAAC[C/G]TTTTCTTCAGAAAAC	54476
rs531605076	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750653	AATGCATGGGCCACA[C/G]AGAGTTCACTAGGAT	54476
rs531605767	snp	G/T			upstream-variant-2KB	RNF216	GRCh38.p7	7:5781917	TGAAAAGGGTATGGG[G/T]CAGGTGGTTGTGGAT	54476
rs531606756	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667238	CAAGTATTTGTTTTA[C/T]AAAACTGTTTCTGTT	54476
rs531613357	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5779703	GCGTGGTGGTGCGCG[C/T]CTGTAATTCCAGCTA	54476
rs531636794	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5648274	ACCATGCCTGGGTAA[C/T]TTTGTATTTTTAGTA	54476
rs531637168	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5735865	TTTGGGAGGCCGAGG[C/T]AGATGGATCACCTGA	54476
rs531639733	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5642269	CTAGCCTGGGGCACA[C/G]TGGCTCCATCTCAGC	54476
rs531643147	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5745781	GGCACACACCTGTAA[C/T]CCCAGCTACTCTCGG	54476
rs531652745	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5759847	CATGTTGGTCAGGCT[A/G]GTCTCGAACTCCTGA	54476
rs531666667	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656682	TTGTCCTCAAAATAC[A/G]TTAAGGTGTTTTGGC	54476
rs531667496	in-del	-/TAA			intron-variant	RNF216	GRCh38.p7	7:5737546	TAATAATAATAATAA[-/TAA]ATAAATAAATATAAA	54476
rs531668714	snp	C/G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216, RNF216-IT1	GRCh38.p7	7:5662290	CCTGCCACCTTTGGG[C/G/T]AGTTGCATGTCTGGC	54476
rs531683499	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5731240	ACAGTCTGCTAAGAG[A/G]TGTAATAAATGAAAT	54476
rs531700450	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621403	TCATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT	54476
rs531716286	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674783	GGCAGATCACCTGAG[A/G]TCAGGAGTTCAAGAC	54476
rs531716354	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5718211	CATGGCGAAACCCTG[C/T]CTCTACTAAAAATAC	54476
rs531739394	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5731001	TGCACTGAATTTCTA[C/T]CTTTGTGAAAGACAA	54476
rs531745869	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671800	AAGAGACCAAAACTC[C/T]GTCTCAAAAAAAAAA	54476
rs531755783	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5694875	TGTTTTGATTTTGAA[A/C]ATTTATTTATAATCA	54476
rs531756660	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5764515	CAGCTTGGTGTGGTG[C/G]CATGCACCTGTAATC	54476
rs531779179	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665774	CTTAGTTACTCAAAT[A/G]CAGACGACTGTTTCT	54476
rs531804642	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750235	CAGTGAGTAAATCTG[C/T]CTCTTCCTGGCAGGC	54476
rs531813673	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5769123	CAGTTCCAAATGCCT[-/T]TTTTTTTTTTTTTTT	54476
rs531819803	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5686927	TGACAGGAGGCAGAG[C/T]TCAGGTCGTAATGCT	54476
rs531822501	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5700819	CTGCCCGCTGCCATG[A/G]GTGGGCAGGATGACC	54476
rs531827438	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5640868	TTGAACAGATACATG[C/T]GTAAGTTTCCTTACT	54476
rs531839604	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5745020	CTTTTTATGAAGTCA[C/G]AATCATGCTTATAAA	54476
rs531847174	snp	A/C	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5716440	ACTCTAAAGTGATAT[A/C]TAAGTTGTAAACTTT	54476
rs531869985	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5626626	GCAGTGATCGTGCTA[C/G]TGCACTCCACCCTCC	54476
rs531870199	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5621217	TTTGCTTTTGTTGCT[C/T]AGGCTGGAGTGCAGT	54476
rs531875670	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5689277	CTAGTTTGTGAGGTA[C/T]AGGAAAAGTGACAGA	54476
rs531880213	snp	C/G			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712064	TGAATATAAACCACT[C/G]AATAAACACGTCCCA	54476
rs531890220	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5654308	ACTATCTAATAAAAA[G/T]AATTTAAAAAGGGAG	54476
rs531890350	snp	C/T	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768881	TTAGCCAGGATGGTC[C/T]TGATCTCCTGACCTC	54476
rs531898844	snp	A/C	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5739712	GCCTAGATAAAAACA[A/C]CTGGGTGGCCGGGTG	54476
rs531907405	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711427	GCAGGGGCTATTTGA[A/G]CACAGGTGGTGAAGA	54476
rs531930119	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5636342	ATAAGACTCTTAGTT[G/T]AATGCTTTTGGCTTC	54476
rs531940594	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5718907	CAAGTGATTGCCTGC[C/T]TTGGCCTCCCAAAGT	54476
rs531944202	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5773523	TGAGATTACAGGAGT[G/T]AGCCACCACACCCAG	54476
rs531944505	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5779010	CGGCCTCCCAAAGTG[C/T]TGGGATTACGGGCGT	54476
rs531945216	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672409	AGAGTTATGTTTGTT[A/C]AATTTAATAACAAGA	54476
rs531954979	snp	C/G	0.00159617	0.0282053	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620402	TGCTCTCTGGGCACT[C/G]GCACGGCCCCTTGCT	54476
rs531964398	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5710912	GTGACAATTGTTATA[C/G]CAACAGCCTGGGGTG	54476
rs531980175	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5693666	ACTGTAGGTCTTTTG[A/G]TAAGAGGAAATTCCC	54476
rs531991209	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620636	TCCCCACCAGCCCAG[C/T]GTGGCCAGAACAGCT	54476
rs532013672	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5635695	GAGGACAAATGACCC[A/G]GGTGGAAACCCAGGC	54476
rs532027225	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5725561	CATGGCTAACAATTG[A/G]TAGTGGCAGCTGGGT	54476
rs532037717	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5705864	GTGAGCCAAGATCAT[A/C]CCATTGCACTCCAGC	54476
rs532040901	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5721479	TCACTACTGAGGACA[C/T]TTGGGTTTGCTGTTT	54476
rs532044948	snp	A/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5645932	TACTTGTTCATACAC[A/T]GTGCTCCTGGTTTCC	54476
rs532068187	snp	G/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5651424	TTTTGTAGAGATGAG[G/T]TTTTACCATATTGCC	54476
rs532068248	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5769710	ACCTGGGAGACAGTG[A/C]GAGCTGTCTCAAAAA	54476
rs532083161	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5646450	TGTAATCCCAGCACC[A/T]TGGGAGGCAGAGGCG	54476
rs532086721	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5631106	GAAACCTCCTTTCTC[C/G]CCTTACAAGACGTAA	54476
rs532122584	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5759108	GTTGTTTAAAAGTGT[G/T]TGGCACCTCTTCCCC	54476
rs532122733	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753990	ACAGAGTGAGACCCC[A/G]TCTCAAATTTTAAAA	54476
rs532130709	in-del	-/C	0.00557542	0.0525036	intron-variant	RNF216	GRCh38.p7	7:5641770	CTGAGCATGGTGGTG[-/C]ACGCCTGTAATCCCA	54476
rs532134463	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5734158	AGAGTTCAGGAGACA[A/T]GCAGGAGAATGTTCA	54476
rs532140094	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5765068	AAGCAAGACTCTCTT[-/A]AAAAAAAAAAAAAAA	54476
rs532146085	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5698123	AGAAACTCTCTTAGC[C/T]TGTTTATTTTTGAAA	54476
rs532161998	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5733927	TTCATTGTAAAAATG[G/T]AGTCATTGCTGCTCA	54476
rs532178772	in-del	-/A			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674467	AGCCCTACATCTCTT[-/A]AAAAAAAAAAAAAGG	54476
rs532179516	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5651015	TGCTTGCCTTGCCCA[C/T]GTGACAATCTAGACC	54476
rs532257966	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5715976	TCAAACCCCTGACCT[C/T]GTGATGTGCCTGCCT	54476
rs532263618	snp	A/G	0	0	intron-variant	RNF216	GRCh38.p7	7:5624463	GTTTGGAGAGGGCTG[A/G]GTCTGAGTGGGCACA	54476
rs532287071	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5629796	GGTGCCACTGCACTC[C/T]AGCCTGGGCAACAGA	54476
rs532289694	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5683166	AGACACCAGACCACA[A/G]GCTAGAAATGCAGCA	54476
rs532291078	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675555	GCTGAGGCAGGGGGA[C/T]TGCTTGAGCCCAGGA	54476
rs532307715	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5624805	AGTGCAGGCAGATGT[A/G]GGAGCTGTGCTGGGA	54476
rs532332030	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681874	ATTCAAAAGCAAGTT[C/G]AACATGAAGACGGGA	54476
rs532336269	snp	A/G	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5777163	ACAAGGCATGTGAAC[A/G]AAGAAGACATTGTGG	54476
rs532360246	snp	A/G	0.00557542	0.0525036	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675575	TGAGCCCAGGAGGTC[A/G]GGCTGCAGTGAGCTA	54476
rs532360862	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768694	TGGGACAGAGTCTTG[C/T]TCTGTCGCCCAGGCT	54476
rs532371238	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5777590	AAGGAATCAAAGTTG[A/T]CCTAGACGCTGAGAT	54476
rs532387759	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5763620	CTGTCATCCTGGCTG[C/G]AGAGCAGCTACACGA	54476
rs532408327	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5730048	TTGAAGTTTTTAAAA[A/C]CCAAACTGTTTACAT	54476
rs532414781	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5761852	CAAGTATGTAAGACA[C/T]GGGAAATCATCTTAT	54476
rs532415896	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5715016	TAGACTCCAGGAATG[C/T]GTCCTATATACATGG	54476
rs532421983	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5660655	CAATCTTGGCTCACT[A/G]CAGTCGCGACCTCCC	54476
rs532457927	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5772527	TTCAATCCTTTCCTT[C/T]CTCTCTGAGAAAATC	54476
rs532488418	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5758796	AGGTGGAAGGGACTA[A/G]ACTTGTCACAGATAA	54476
rs532519505	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5635505	TTACCAGGTTTCTGC[A/G]TTTCCTCATCAATCC	54476
rs532530090	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5748676	ATATACTAACTAAAG[A/C]ATGTTAACCATGTTA	54476
rs532573935	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5714780	CTCTTTCTGAGGTAA[C/G]CTTCCCTCTGAATAC	54476
rs532580664	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5743031	ATTCAGGGAGGCCAA[C/G]GCAGGCGGATCACGA	54476
rs532580831	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5654305	TGTACTATCTAATAA[A/C]AAGAATTTAAAAAGG	54476
rs532597414	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5655940	CGGCTTACTGCAACC[C/T]CCACCTCCTGGGCTC	54476
rs532604348	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674178	GGGATTATAGGCACC[C/T]ACCACCACGCCCAGC	54476
rs532636089	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5709905	GACTATGGGCACACA[C/T]CACCATGCCTAGCTG	54476
rs532640864	in-del	-/TTTTTTTTTTTTTTTTTTTTTTTT	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5740105	ACCAGATGTAACACC[-/TTTTTTTTTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTG	54476
rs532645130	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5654141	AAGCCACTCAGGAGA[C/G]AGGCCATGAAGGCCC	54476
rs532660572	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5684238	CTCCGGAGTAGTTAG[A/G]ACTACAGGCACCCGC	54476
rs532670396	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5738252	TAAAATAAGAGACAA[A/G]GTCCCACTCTGGCTC	54476
rs532671343	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670734	CACAGTATGTTGAAA[C/T]GTGACTTCCCTCTCA	54476
rs532712388	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5687311	TGAGGAGGGAGAATC[A/G]CTTGAACCTGGGAGG	54476
rs532712616	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5724666	CTTTCCAGCTTTATA[A/G]TTACCTGAGTTTCCA	54476
rs532714271	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681384	CCTTGGCCCCAAACA[C/T]GTCACATTTTATAGC	54476
rs532772302	snp	C/G	0.0023933	0.0345097	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664088	TAGATTTGAGCGGCA[C/G]AAGGTGCTGAATGTC	54476
rs532773104	snp	A/C	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5722852	CATGGTGAAACCCCC[A/C]AGGCATGATGGCGCA	54476
rs532786937	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5654826	CCTCACCTACATCCC[A/G]TTCAGTAAACAAAGG	54476
rs532807398	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5649998	CATGCAGATAGAACC[A/T]GGTGAACAGGAAGTA	54476
rs532814631	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5762065	ATTATAGCAAATATG[C/T]AATAAAAGCAATTGG	54476
rs532824529	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5743737	CAACAGTTCCTCTGG[A/G]AAGTCCCTAGAAGAA	54476
rs532828045	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5732822	AGCTGATCTGACATG[C/T]TAGCAGTTCTAGAGA	54476
rs532841279	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753183	TTTTGGGAACTGCTA[A/G]AGAACATCTAACAAT	54476
rs532860218	snp	A/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5644422	TGATTTGTATTTCTG[A/T]AATGACTAATGACGT	54476
rs532860658	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5728538	GAGATTAGGCCACTG[C/T]ACTCCAGCCTGGGCA	54476
rs532878776	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5720257	CCTGAGACAGCAAAA[C/T]CAACACACCCCTCCT	54476
rs532892415	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5691590	AGTTTTAAGTCTATT[C/G]TTTAAAATGCCCAGC	54476
rs532901773	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5762582	CTGATATCCCAGCTA[C/G]TCAGGAAGCTAAGGC	54476
rs532903937	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5757285	TTTCCTATCATGTTA[C/G]TAAGTATACAGGGAT	54476
rs532936181	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669562	TAAATCAAGACCTAA[A/G]CTTTGTATCAAATCT	54476
rs532967603	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5772005	TTGGAAGGCCGAGGC[A/G]GGTGGATCACCTGAG	54476
rs532994618	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767487	TAACCTCCTCACCCC[C/G]CACCAAGTTGTTAAC	54476
rs533013836	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713414	GGAGAGCAGAGCTGA[A/G]GGGTGGCCTGAAGTC	54476
rs533040698	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643811	CCCCAAAAGGAAACC[C/T]TGTACCCACTAAGCA	54476
rs533044300	snp	C/T	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753883	GCCTGTAATCCCAGC[C/T]ATTCAGGAGGCTGAG	54476
rs533050242	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5703511	AACCAACAAACTGGT[C/T]CACTGCAGATGTGAA	54476
rs533056721	in-del	-/CTGAGAGCCTTCCATCAGTGCCG			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662622	CTTCCACCAGTGCCA[-/CTGAGAGCCTTCCATCAGTGCCG]CTGAGAGCCTTCCAT	54476
rs533060385	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5637992	CTGGGAGGCCCTCCC[C/G]GCAACAACCTGTAGT	54476
rs533087118	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5623707	CTGAGGAGCTGGGAT[C/G]GCAGATGTGTGCCAA	54476
rs533096027	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5628865	GAAGTTCCTTCCACA[A/G]TCAGTTTCTCTGAAG	54476
rs533097270	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5632994	AGCACTTTCTGTTTT[C/T]TTTGAGACAGAGTCG	54476
rs533102811	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5771254	CTCATGCCTTACACA[A/G]AAACAATTTTAGATA	54476
rs533124728	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780732	AAAAAAAAAAAAGTA[A/C]AAGAAAAAAGAACGT	54476
rs533143587	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5727135	AGCGGGGTGGCTATG[A/C]TGCAGTGTTTGCCTG	54476
rs533144947	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5752120	AAACCAGAAGGCGGA[A/G]GTTGCAGTGAGCCAA	54476
rs533148705	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622111	CTCTGTCCCAGCTGC[C/T]TTAAGAGGCTCTTTC	54476
rs533155019	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5657561	AACAAGAGTGAAATT[C/T]TGTCTAAAAAAAAAA	54476
rs533178249	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5747418	GAGGATGATATTCAG[G/T]ACCTGACAAGTACTA	54476
rs533190602	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5688926	AGTCTGAACTCAAAT[C/G]TTGACTGAATGAGAG	54476
rs533201464	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5722848	CCAACATGGTGAAAC[C/T]CCCCAGGCATGATGG	54476
rs533213866	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5723167	TTTGAAACATAAATG[A/T]ATTAATCCATTAAAG	54476
rs533215425	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5653348	GTAATCCCAGGAATT[C/T]GGGAGGCCGAGGTGG	54476
rs533216660	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5708056	TCATACTTTGTGAAT[A/T]TTCTTGCTGTTTGTG	54476
rs533221899	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5648597	GCCAGGCATGGTGGC[A/G]GGCACTCATAGTCCC	54476
rs533256059	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5771409	TGAAACACTATACAT[C/T]AAAATTAAGCATGTC	54476
rs533260445	snp	G/T	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5749415	CTCGGCCTCCCAAAG[G/T]GCTGGGATTACAGGC	54476
rs533264679	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5776511	GAGGCAGGAGAATGG[C/T]GAGAACCCGGGAGGC	54476
rs533267600	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5751523	AACCAGTTTCTTAAA[C/T]AGGGCAGTTTAAATC	54476
rs533271511	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5736804	AGCAGCGTCTCTGCC[C/T]GGCCGCCCCGTCTGA	54476
rs533281160	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5708685	TTGCAAGCTCTTGCT[G/T]CTTCTGGTGCCTGTC	54476
rs533283846	snp	C/T	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5628458	AATACAACTTAAAAG[C/T]TTTTTTTCTTTTTTA	54476
rs533288333	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5718343	CCGAGATCCTGCCAC[C/T]GCACTCCAGCCTGGG	54476
rs533304648	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5751686	TAACTTTGAAAGGAC[A/T]TTGCTTCTGCTCTCT	54476
rs533314839	in-del	-/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5722090	ACCACACCCAGCTAA[-/T]TTTTTTTGTATTTTT	54476
rs533321104	in-del	-/A	0.330714	0.236612	intron-variant	RNF216	GRCh38.p7	7:5629461	AAGATCCTGTCTCAG[-/A]AAAAAAAAAAGTGAA	54476
rs533321558	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5732208	TCCTAGAATTCACTG[A/G]TGTGCACTGAGGTTA	54476
rs533324088	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665982	GATCCTGGCTAACAC[A/G]GTGAAACCCCGTTTC	54476
rs533336313	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5756068	GCGGGACAGGTGGAG[G/T]TAATCGGATCATGGG	54476
rs533341821	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5761513	TATGTTTCAGCCAGA[C/T]GCAGTGGCTCACGCC	54476
rs533374530	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622638	AGGGGCAGTTCACAT[C/T]GCAGCTCTCTCCGAA	54476
rs533379849	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5626758	TAGCTAAGTGAGCTC[A/G]GCAGGTTCCTGAGTA	54476
rs533381805	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5649902	CTTTTCCTGTCTGTT[C/T]GATAATCAGAGAACA	54476
rs533399274	in-del	-/TAC	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5635491	TAAAATACCTTTCCT[-/TAC]CAGGTTTCTGCGTTT	54476
rs533399969	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736356	CCAGCTCCTAACCGG[A/G]ACTGATCTGCCAGCC	54476
rs533411743	snp	A/T	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5765464	GTGAGACTCCATCTC[A/T]AAAAATAAAAAAATA	54476
rs533422898	snp	A/C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5653792	CTGAGATCCAAAGGA[A/C/T]GAGTCAACGATGAAT	54476
rs533429161	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5751121	TGCTGTGCACCCTCA[C/G]AAAGTTTTAAATGTT	54476
rs533440946	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5632522	GAACAAGCGTAATGA[C/T]GTGTCAGGCCAGGGT	54476
rs533445035	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5626732	CAGGAGGGCCGTGGG[A/C]CTACACCTCTTAGCT	54476
rs533447478	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5687328	TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC	54476
rs533448243	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5685452	GAGGGCAGGGCTATA[C/G]AAATTGTTCTGTTAC	54476
rs533481842	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5627198	GTTACGGCTAGTTGG[A/C]GGTAAACTGGGACAA	54476
rs533496764	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5746954	AGAATTCTAAAATAG[C/T]TTTTTTGAAAGATTA	54476
rs533504258	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5654906	ACAAACCCATTTTTA[A/T]AAGAAACAAACCCTG	54476
rs533511907	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5685930	TTGTAGAAAACGATG[C/T]AAAAAATTCCGGCCG	54476
rs533521605	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736022	CACTTGAACCTGGGA[G/T]ATGGAGGCTGCAGTG	54476
rs533551295	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5777033	ACTTAGGGCTCCTGG[A/G]CCCAGAGTCATCAGG	54476
rs533558237	snp	A/C	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675969	CCACCTCAGCCTTCC[A/C]AAGTGCTGGGATTAC	54476
rs533560765	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667985	GCTTCAAGCTGAGCA[A/G]GTAACTTCGCGTTGG	54476
rs533563543	in-del	-/AT			intron-variant	RNF216	GRCh38.p7	7:5653245	ATTCTAGGATCCTTC[-/AT]AGTTTATAAAATGCT	54476
rs533570368	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673631	TTCTCCATTTGGCTA[C/G]ATCTGGAGAATAAAA	54476
rs533574887	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668472	TCGTGATCTGCCCGC[C/T]TCGGCCTCCCAAAGT	54476
rs533574981	snp	C/T	0.00159617	0.0282053	intron-variant, nc-transcript-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662439	CTTGCCACTTACCTC[C/T]TCAAAGGTGGCCAGG	54476
rs533575193	snp	A/C	9.23574e-05	0.00679486	intron-variant	RNF216	GRCh38.p7	7:5641111	TAAAAATATATTTCT[A/C]TTTTCTCCCTATAAA	54476
rs533581046	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5765168	AAGAGCTATTAAAAA[A/G]ATGAACTTCAAGACC	54476
rs533584085	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5706105	TGTGCCTGTAGTCCC[A/G]GCTATTCAGGAGGCT	54476
rs533596324	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5706324	AAAATGTTGTACAGC[C/T]GATCTCTAAACAACT	54476
rs533598701	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5635936	TGGACAGGTTTCAAA[A/C]TCTTACATTCAAAAG	54476
rs533627014	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5631127	CAAGACGTAACAGGA[C/G]AAAACAAAACAAAAC	54476
rs533639403	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5769939	GGCTGAGACAGAGGA[A/G]TCACTTGAACCCAGG	54476
rs533639701	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662856	TTGTGTAGAGCTGGC[A/C]CTTCTGCTTGAGCCT	54476
rs533662672	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5631692	AAATGCCATTATTTC[C/T]TTTCCTTATACATAT	54476
rs533669317	snp	A/C	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5700273	TGCACTCACACACAG[A/C]CCCTTCTCAAGGACA	54476
rs533669489	in-del	-/GGTT	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5635496	TACCTTTCCTTACCA[-/GGTT]TCTGCGTTTCCTCAT	54476
rs533669856	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670856	CCATATAAGGAGGCC[A/G]TCTGTAGCCTTTTTC	54476
rs533728725	snp	C/G	0.00835141	0.0640778	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754434	CCCAAGAAGTCACTG[C/G]GATGACAGGCATGAG	54476
rs533777699	in-del	-/GCAGGATGG	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669127	CCAGTCCCGTGCTAT[-/GCAGGATGG]GCAGGACTGTCTGCA	54476
rs533811576	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5735374	GAAGAACAGAATATG[A/G]TTCCCAAGAACTTAA	54476
rs533821449	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5683522	GGCCACAGGCACATA[A/G]CATCATGACTTAACC	54476
rs533822642	snp	A/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5778808	GAGTGCAGTGGCACA[A/T]TCTCGGATCACTGCA	54476
rs533830986	snp	A/G	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5747338	CAGCTAACACATGGT[A/G]GGACCAGGGGAAGGA	54476
rs533838319	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5699946	TCAGCTACCACATTG[C/T]AACTGGAATCTGACC	54476
rs533898489	in-del	-/T	0.498503	0.0273153	intron-variant	RNF216	GRCh38.p7	7:5705922	AACAAAAACTAAAAC[-/T]AAAACAAAACAAAAC	54476
rs533899497	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5764593	GCGGAGGTTGCAGTA[A/G]GCCAAGATTGTGCCA	54476
rs533905194	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5694161	GAAGAATCCAGAAAG[A/G]TCTTACTAAAAAGGG	54476
rs533957998	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5651101	CATAAAGAAAAGCTG[A/C]CTGCTTGGCAAGTTG	54476
rs533961659	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5692966	TGTCTGTGTCAGCAA[A/G]CATCTCTTCCTCCTC	54476
rs533969944	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5749285	CCTCCTGAGTAGCTG[C/G]AATTACAGGCACGTG	54476
rs533996144	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5723656	CGTCTCAAAAAAAAA[A/T]AATAAATAAATAAAT	54476
rs534007639	snp	A/G	0.00597247	0.0543191	intron-variant	RNF216	GRCh38.p7	7:5655860	CGAAGAAACGCTCTT[A/G]AATGGTTTTTTTTTG	54476
rs534009086	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5646153	ATACTGAGAAGAGTC[C/T]AGAAATCAGGTTGCT	54476
rs534034398	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5624968	CTGCTTCATGAGTGG[C/T]GCTTACCTTAACCCC	54476
rs534036961	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5688327	ACATATCTGGAAATC[A/G]TAAACAAGGGGCTGC	54476
rs534048959	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5744304	AGAGAAATTAGTGCA[C/T]TGAAAGCCAGGTCAG	54476
rs534050052	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667125	ATGACTTTTAAACTA[C/T]AAACTGTGGCCCTAT	54476
rs534055017	in-del	-/ATCAGTCAGCTTGA	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5766700	TTGTTAGTCTATGGT[-/ATCAGTCAGCTTGA]GCTGACTAATACAGG	54476
rs534056637	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5745280	AATGTAACAGAATCC[C/T]ACATTCACTTCTAAA	54476
rs534069990	snp	A/G	0.00199481	0.0315187	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620453	GTGCTTCTCTCCCCA[A/G]TGCTGTCACTGGTCC	54476
rs534088827	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670458	GGTTGGGTAAAAAAA[G/T]TCTTTTACTTCCTCT	54476
rs534097781	snp	A/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5635374	GCTGTGGAAGCTGGG[A/T]GATGGGACAATCTGG	54476
rs534106256	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5772362	TTCCATGGACAACAG[C/T]TACAAAAAAACTAGA	54476
rs534108490	snp	A/C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5714947	AAGCATACCAGCAGA[A/C/T]CTCCACCTCACCCTC	54476
rs534117032	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5743253	GAGACAGAGCAAGAC[C/T]CTGTCTCAAATAAAT	54476
rs534121652	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5737915	CAACATGATGAAACC[C/G]TGTCTCTACTAAAAA	54476
rs534126103	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671620	CCAGCCTGACCAACA[G/T]GGTGAAACACCGTCT	54476
rs534143294	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665097	ACCACCGCACCCAGC[C/T]AGGACACACAAAATT	54476
rs534147210	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670881	TTTTTCAGGGGTGAG[A/G]GTCCACCCTGGGAAG	54476
rs534158174	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5624529	TCGGCATGGCAGCCT[A/G]TCTGCAGAGCCTGGA	54476
rs534169539	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5704241	TTATATTAATGCCGT[A/T]TTAATATAAACGCCT	54476
rs534194422	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5660361	CAGTGGCGCAATCTC[A/G]GCTCACTGCAAGCTC	54476
rs534197282	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5725020	ATTCGCATCAAACCT[C/T]TGAGACCAGTTTTTC	54476
rs534197303	in-del	-/A			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780716	CTCAAAGAAAAGGAG[-/A]AAAAAAAAAAAAGTA	54476
rs534205061	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5655535	TGCTTGAACCTGGGG[G/T]GCGGAGGTTGCAGTG	54476
rs534207796	snp	C/G			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680952	CAGCCTAGATCCCCT[C/G]TGGCTGGGCCATGGC	54476
rs534248924	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5763365	GCTAGGAGCGATGGC[C/T]CACACCTGTAATCCC	54476
rs534255653	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5650720	ACTCTTCGTCCCACA[C/G]TAAGGACTTTCTGCT	54476
rs534265630	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5630252	AAGAGAGGCTGCTGG[C/T]GTCACGGGAAGAACT	54476
rs534267824	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5705246	CGTACACACTGGATG[C/T]CTCCCCTAAAAACTC	54476
rs534297417	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620120	TTACACACAGTAGTT[A/G]AAACGGAATTATTTT	54476
rs534298716	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5654966	AAACAACAGCTGGAG[A/G]ATAGATGAGCTGATG	54476
rs534312029	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5649702	CTAAGATGCAGAGGC[A/G]ATGATTCTTTCACAT	54476
rs534353720	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5644205	GTGAGTACCTGAGAG[C/T]GGAACTGCTGGGTCA	54476
rs534362488	snp	A/G	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5777675	TCAGAGAAAGAAAAC[A/G]AAAATTGTGTTAACT	54476
rs534413077	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5742710	AAGCAATTATCCTGC[C/T]ACAGCCTCCCGAGTA	54476
rs534429894	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5738387	TGAACCATATGTCTG[A/G]CCCGTATTTATCCCT	54476
rs534439706	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5634141	TTTTGAGACTTTTTT[C/T]CCAACACTTCTGGTC	54476
rs534461012	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5704776	GTCACTGAGCCAGCT[C/G]CACCAGGCCGTCACT	54476
rs534477414	in-del	-/AGC	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5656789	ATGATTAATGAATAA[-/AGC]AGAAGATTAAATTCA	54476
rs534484429	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5728573	GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAGAAA	54476
rs534510349	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5732912	TTGCTGCCTTCATCC[A/T]ACTGAAGCTGACCAC	54476
rs534512946	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5658474	CCAGCCTGGCAAACA[C/T]AGTGAGACCCCATCT	54476
rs534522530	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5642047	TAAAAAAAAAAAAAG[-/A]AAAAAAAAAAGAAAG	54476
rs534553775	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678788	TCACACAGAAGGTGA[C/T]GGAGCAGATTTCTCG	54476
rs534573136	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5687068	ACAGTCAAGTGAATG[G/T]TATAGAAACACCAGG	54476
rs534592521	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5765377	GCTGAGGTAAGAGAA[C/T]TGCTTCAGCTTGGAA	54476
rs534599016	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5724044	AACTGAATCAAATGA[A/C]ATGAAGTTAATGGGA	54476
rs534628429	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5729132	TGTCCCAAGTTGGAA[A/C]GCAAATCAGGAAGGA	54476
rs534652236	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5687937	GGTCGTGTCCAGAAT[C/T]CCGGACTGTCATGCC	54476
rs534652490	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782126	GGAGGCCAAGGCGGG[A/T]GGATCACTTGAGGTC	54476
rs534669552	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5714511	GATCCGCCTACCTCG[C/G]CCTCCCAAAGTGCTG	54476
rs534684206	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5644604	TCCGCCTCCTGGGCT[C/G]AAGTGATTTCCCACC	54476
rs534692051	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782619	CATTGGGAGGCCGAG[A/G]CAGGCAGATCACTTG	54476
rs534694060	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5777305	AATTATTCTATGAAG[C/T]AGTAAGTATTAGGGT	54476
rs534734580	snp	A/G	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5736860	AGCCACCCCATCTGA[A/G]AAGTGAGGAGCCCCT	54476
rs534751135	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5708903	CAAAAAGCAGCCTTC[C/G]AGGTGCACTGGACTC	54476
rs534762658	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5702466	TCGGGTTGTCAGCTC[G/T]CTCCCTTCTGAATAA	54476
rs534765861	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675674	CAAACGAACAAAGGA[A/G]CAAGGTCATGAAGCC	54476
rs534805492	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5627901	GCCACTGCCTGATTT[G/T]TATCACTAAGCTTCC	54476
rs534807087	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664304	CCTTTCAGGTTAATT[C/T]ATTACAGCTTCAGCC	54476
rs534811417	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5633553	GCACTCCAGCCTGGG[C/T]GACAGAGGGAGACTC	54476
rs534822115	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5659033	TATGAAAGAGATGAG[A/G]GTGAGAGAGAAGCCT	54476
rs534823443	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5696440	ATGTAAAGCACCTGA[C/G]GACTAAAACAAATTC	54476
rs534839640	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663741	TGTCTCTACTAAAAA[C/T]ACAAAAATTAGCCGG	54476
rs534844914	snp	C/T	0.00835141	0.0640778	intron-variant	RNF216	GRCh38.p7	7:5697077	CCTCAACAGGGTCTA[C/T]TTATCTTCAAAGTCC	54476
rs534868847	snp	A/C	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5762709	AAACAAACAAACAAA[A/C]AAAAAAAAAATTAAA	54476
rs534892997	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5722958	TAAAATTAAAAAAAA[A/C]AACAGCAACAAAAAA	54476
rs534895375	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5689421	AACATCCAAAGCCGA[G/T]GAGGCAGGGCGCCTA	54476
rs534912480	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5692214	AATGGGAATTTTTTA[G/T]TTGTTTATATGTACA	54476
rs534926074	snp	A/C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5686561	AATCTGTACAATGCA[A/C/T]GCCAGTGTTCCTAAA	54476
rs534935908	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780552	AAATACAAAAATTAG[A/C]TGGACGTGGTGGCAA	54476
rs534960464	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5757857	GGTTGATGCATAATA[A/G]AAAATTATTAATGTT	54476
rs534972170	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780803	AGGCCCTTAGGGATT[C/T]ACAGAGCCCTGTCGG	54476
rs534977836	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5643095	GAAAAAAAGGCTCTC[C/T]TAAAATGGACAGAGG	54476
rs535006586	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5758469	GAGCAACACTGATTT[C/T]AACAGTGTGGGTCCC	54476
rs535032875	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5744530	CTAAATAAGGGAAAA[A/T]ACATAAGGAGTCACA	54476
rs535038030	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669211	CTACTAAGCAGAGTT[C/G]CATCTGACAAGATCT	54476
rs535062479	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5638070	CGCAGTCCCCACTAT[A/G]CCTTCCTGCCTCCTA	54476
rs535095305	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662643	GCCTTCCATCAGTGC[C/T]GCTGAGAGCCTTCCA	54476
rs535096919	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5765614	CAGCCAGGGTGAGAG[A/C]GAGACCCTGCCTCTG	54476
rs535108231	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5695205	TGACCTCCTGGGTCC[A/G]GCTTATAAATCTAAC	54476
rs535111277	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5657365	CTGAGGTTGGGAGTT[C/T]GAGACCAGCCTGACC	54476
rs535120710	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5650566	TGAGGTTGTAGGACC[A/G]GGGTCTCTATTTTCT	54476
rs535151710	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5766948	CCAGAGGCTAAAAGA[C/G]AGAATAAAATTACAA	54476
rs535158918	in-del	-/TT	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780820	CAGAGCCCTGTCGGA[-/TT]TGTCAGAAATTTCTG	54476
rs535159189	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5761251	ATTCCTTAAGAAAAC[A/G]TATCCAAGGAGGTGG	54476
rs535166828	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5695561	TGCAGAGCAGAAGAC[A/G]CCGCAGCTATAGACA	54476
rs535187432	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5690600	AGTGCTTTCCCTGTA[C/G]ATCTGCAAGCATCAC	54476
rs535198797	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5756834	GACATGAGAATCTCA[A/C]CATGTCGCCCAGGCT	54476
rs535210920	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5751311	TTTGGTCAGGTCCTG[C/G]GTGAAAGCCTAACAA	54476
rs535225864	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672817	TGCTGTAGAGCACTG[A/G]GAGGCGAGGAGCTGG	54476
rs535226459	in-del	-/GGT	0.336474	0.234568	intron-variant	RNF216	GRCh38.p7	7:5658560	TACTTGGGAGGCTGA[-/GGT]GGGGGAGGATTTCTT	54476
rs535265576	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5779847	AAAAAAAAAAAAATG[C/T]TCAATGAATGGGCTG	54476
rs535287772	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5718489	AATTTTTACAACCTT[A/G]GACAAAAAAACAAAA	54476
rs535298117	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5774999	ATCCACCCCCCCGAC[A/G]CTCACCAAAGTGGTG	54476
rs535300460	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5746693	CCTAATTTCTAAAAA[C/T]TGGAGTACTCTGCCT	54476
rs535307116	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5649110	CGGCCGGGCGGGCGC[A/G]GTGGCTCACGCCTGT	54476
rs535361780	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5740454	TAATATCACCACTAA[C/T]AGAACTTTGTTGGAT	54476
rs535368185	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5735827	AGGCCAGGTGCAGTG[A/G]GTCACACCTGTAATC	54476
rs535388046	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674186	AGGCACCCACCACCA[C/T]GCCCAGCTAATTTTT	54476
rs535389513	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668171	CTGCCCCTGGTAGTT[C/T]TTCACATTCTCATAA	54476
rs535389595	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5765273	TGAGACCAGCCTGGG[A/C]AACACAGTGAGGACT	54476
rs535420729	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768754	GCAAGCTCCGCCTCC[C/T]GGGTTTACGCCATTC	54476
rs535430091	snp	A/G	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5736455	GCAGTGCAGTGGCGC[A/G]ATCTCGGCTCGCTAC	54476
rs535437281	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656737	ATATAAAGAAAGCAC[C/T]TCCGTCTTCCTTTAT	54476
rs535448717	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5760707	TCCTTTATAATCACC[A/T]CGCCTTCAAAAACTG	54476
rs535456274	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5726814	AGTGAGCTGAGATCG[C/T]GCCACTGCACTCCAG	54476
rs535456571	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5732013	ACTTCAGGAGTCCCA[C/T]ATACTCTTCATCTCT	54476
rs535471143	snp	G/T	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5726214	CCTGAGAGGCAGGGT[G/T]GCAGTGAGCCATGAT	54476
rs535479918	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5661722	GCATGAGAATCGTTC[A/G]AACCTGGGAGGCAGA	54476
rs535493353	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5764954	ACACATCTGTGATCC[A/C]AGCTACTCCTGAGGC	54476
rs535502759	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5657749	ACCCATACGCCCAAA[G/T]GACATACAGAAGGCC	54476
rs535531279	snp	C/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5627359	GAGTGTGGCAGCCTT[C/G]GCCCTCCTTGTGAGG	54476
rs535532251	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5684342	TCGATCTCCTGACCT[C/T]GTGACCCACCTGCCT	54476
rs535535927	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5637293	AAAAGAAGGATGACT[C/T]GGGCTTGGCTTTCTA	54476
rs535550205	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5647112	CCCTGAGGAAGTTGT[A/G]AAAGGTGAAAAAAAA	54476
rs535564653	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5684288	TTGTTTTTGTATTTT[C/T]AGTAGAGACGGGGTT	54476
rs535588581	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5641834	GAGCTCAGGAGTTTG[A/G]GACCAGCCTGACCAA	54476
rs535613697	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5630989	TGAGAACACTGCTGT[C/T]GGGCTGGGAGCGTGT	54476
rs535615347	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5708717	GAGGTATCACAGGCC[A/C]TCTGGAGCTGCTGTA	54476
rs535624465	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5739977	CACTGTACCCCAGCC[G/T]GGGTGACAGAGTGAG	54476
rs535646368	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5752399	TATCATAAAAATTGC[G/T]CTATAAATATAACAG	54476
rs535650807	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5735337	AATACACAAGAAAAC[C/T]AGGCACCATGGGAGC	54476
rs535665205	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666755	CCTTCCAAAGGATTT[C/G]CTCCCCATAGATGCT	54476
rs535668315	snp	C/G	3.7477e-05	0.00432864	intron-variant	RNF216	GRCh38.p7	7:5730697	GCAGTGACTGCAAAA[C/G]ATGAACATGACACTT	54476
rs535677139	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5661340	AGCCTGAACTTACAG[C/G]TGTGCGCCACCATGC	54476
rs535687989	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5642330	GAGATTCTCCCACTT[A/C]AGTCTCCCAAGTAGC	54476
rs535696349	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5699868	TGACAGAGACCCTCT[A/G]TATTCTTTATCTTTG	54476
rs535704826	snp	A/G			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622703	TCCACTCTTCCAGGA[A/G]CAGTAGCCCTTCTAG	54476
rs535726198	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5770393	TTGAACCTGGGAGGC[A/G]GAGGTTGTGGTGAGC	54476
rs535733903	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5637047	CTGCCCTTTGTCTCT[A/G]GAGATGAAATACTGC	54476
rs535769978	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5625482	CCAGAGCAGCAACTG[A/G]AAGGAAGACAATCCT	54476
rs535773753	in-del	-/AAAAAAAAAAAAAAAAAAAAG			intron-variant	RNF216	GRCh38.p7	7:5747756	CATCTCAAAAAAAAA[-/AAAAAAAAAAAAAAAAAAAAG]GGGAAAAAAAAAGAA	54476
rs535774016	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5643695	AATGCACATAAAATT[C/G]ACTTTTTAAACCACT	54476
rs535814318	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5759900	TCTCCCAAAGTGCTG[A/G]GATTACAGGAGTGAG	54476
rs535823936	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5689298	AAGTGACAGAAGTTA[A/C]GCTCAGTTTTTGTAA	54476
rs535831273	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5721635	AAAGTGGTTGTACCA[A/G]TTTACACCCTTCCTC	54476
rs535927418	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5779271	AGATTTCTCCACAGG[A/G]GCTTCAGGAGTTCTC	54476
rs535952544	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5734731	CGGGAGACTGAGGCA[A/G]GAGAATCACCTGAAC	54476
rs535974237	snp	C/G	0.000119574	0.00773129	intron-variant	RNF216	GRCh38.p7	7:5739244	TTACCACCACCACCA[C/G]CACCACAAAAAAAGC	54476
rs535980202	snp	A/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5705977	CAAAACACCACTCTG[A/G]GAGGCCGAAGCAGGT	54476
rs535990905	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5694779	TCTGCCAGGGTGCAC[A/T]GGGCAGAAATTTTAC	54476
rs535997566	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619998	GGACGAATCTGTCGG[C/T]GGCCCCTGTAACTTG	54476
rs536002874	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5625175	GCAAACCCAAACACG[A/C]CAACTGCCGGCTCAG	54476
rs536004951	in-del	-/AAAG	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669890	CTCCATCTCAAAAAA[-/AAAG]AAAGTAAGTGAGATT	54476
rs536038190	in-del	-/AA			intron-variant	RNF216	GRCh38.p7	7:5654712	AAAAAAAAAAAAAAA[-/AA]GGCTCAATCAATGGG	54476
rs536061413	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5725196	AAAATAGTTCCTGTC[A/C]GTCACTCCTTGGACT	54476
rs536074316	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5764050	CAAGAAATTATCCAG[A/G]TGTGGTGGCAGGTGC	54476
rs536075962	in-del	-/TTTTTTTTTTTTT	0.417845	0.185278	intron-variant	RNF216	GRCh38.p7	7:5742587	GGATGGTGAAAAATC[-/TTTTTTTTTTTTT]TTTTTTTTTTTTTTG	54476
rs536079711	snp	G/T	0.00557542	0.0525036	intron-variant	RNF216	GRCh38.p7	7:5758853	ATGAGTTAAGACTTT[G/T]GGGACTGTTGGGAAG	54476
rs536101095	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5759319	GGCATTTCTTTACAG[C/G]CAGTGGAGAACGAAC	54476
rs536109896	snp	A/G	9.9108e-05	0.00703876	synonymous-codon	RNF216	GRCh38.p7	7:5715083	GACTGCCTCTTGGGC[A/G]TATCTGATGAGACAC	54476
rs536123641	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5783361	TCTTGAACTCCTGAC[C/G]TCAGGTAATCTACCC	54476
rs536160895	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5623592	ATGTGAGCCACTGCA[C/T]TTAGCCTCTTTTTTT	54476
rs536168240	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5688945	ACTGAATGAGAGAAG[C/T]GGGAAAAATATTCAC	54476
rs536173415	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5725798	GAGGTCGCAGTGAGC[C/T]GAGACTGCACCACTG	54476
rs536187317	snp	A/G/T	0.000798403	0.0199641	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620999	TTCCAAGGCACTGTC[A/G/T]TTCAGGCTAGTAGCA	54476
rs536190845	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5682532	CCTGCCTCAGCCACC[C/T]GAGTAGCTGGGACTA	54476
rs536214207	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5772615	GATCGGGGCTTCTCA[C/T]TAAATGTCTACAAAG	54476
rs536228670	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5744133	TAACAGCATGTTTAG[A/G]GAAATCAAAGACTAG	54476
rs536251441	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665534	TGGAATAGAAGCTTT[A/G]TATGTGGTTTCTGTG	54476
rs536254399	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768237	AGGAGGATCACTTGA[A/G]CCCAGGAGTTTAAGA	54476
rs536268267	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671590	CGGGCGGATCAAGAG[G/T]TCAGCAGTTCGAGAC	54476
rs536272947	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5697559	TATTCTTTTGTTTGT[C/T]TAAAGAGATGAGGTC	54476
rs536335648	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5737054	GAGAACGGGCCATGA[G/T]GACGATGACAGCTGT	54476
rs536345934	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768898	GATCTCCTGACCTCG[C/T]GATCCACCCGCCTCG	54476
rs536346375	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5698169	TAGTTTTAAAATCCT[C/T]GGTTTTCTAGAAATC	54476
rs536346615	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5692505	CGGGGCCCTGACTTC[C/T]GGTCCAAGGTTTCTC	54476
rs536358819	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5692903	TGAGCATCCTCAAAA[A/G]CGATTCACTGCTACC	54476
rs536364819	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619763	CCTGCAAAAGAAACC[A/G]ACTGCACCTTTCTTG	54476
rs536366422	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5699152	TCGACTCATAACCAA[C/T]CTGAGCTTATCTATA	54476
rs536370118	snp	A/G	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5630656	CCTCCGCCTCCCAAA[A/G]TGCAGGGATTACAGG	54476
rs536375430	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5762316	TCACCTAAGGTGAGG[A/T]GTTTGAGACCAGCCT	54476
rs536378886	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671931	GGCCTCACAAGAAAC[A/G]AAATCTGCTGACAAC	54476
rs536382975	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5769266	GGGACTACAGGCGTG[C/T]GCCACCACGCCCAGC	54476
rs536394619	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5717327	CATTGCACTCTAGCC[A/C/T]GGGCAACAAGAGTGA	54476
rs536428776	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5655452	AAAATACAAAAATTA[C/G]CTGGACGTGGTGGCA	54476
rs536432243	snp	C/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5742225	CTAATTTTTGTGTTT[C/G]TAAGAGAGATGGGGT	54476
rs536438920	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5724904	AATGACAGAATTTTG[C/G]AGAAACGTGGCTATT	54476
rs536461258	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675663	AAACAAACAAACAAA[C/T]GAACAAAGGAGCAAG	54476
rs536464462	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669909	AAAGTAAGTGAGATT[A/G]TGGATGGTGCGTTTG	54476
rs536470098	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5710097	GGGGGTGGTGGCTTA[C/T]ACCTGTAATACCAGC	54476
rs536471980	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5632731	GCAGTGAGCCAAGAT[C/G]ACGCGACTGCATTCC	54476
rs536472120	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753713	TTTTAAAAAAAAGCA[C/T]TGGCCGGGAGCAGTG	54476
rs536486946	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5709143	AATGAGGAGTCAGTA[C/T]GTGCTAGTTTCACCA	54476
rs536511161	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5748913	TAACGAAGGCTATAA[G/T]ATCTGCTTCTCTGTG	54476
rs536520381	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5645655	GTGTGCAGTGGTGCA[C/G]TCTCAGCTCACTGCA	54476
rs536536624	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5653089	AACTCGCTTCTACTG[C/G]ATTGAAGAATGGCCT	54476
rs536537498	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5685693	CACCTCCTCTGCTCT[C/G]AAACTCCCAGCCACA	54476
rs536541892	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5772302	AGTAGTAACAGCAGA[A/G]TAGTCTTTGAATCTC	54476
rs536579088	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767646	TGCTCTGCCACCCAG[G/T]CTGAAGTAATGGTGC	54476
rs536582721	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5723430	AGGCGGGCGGATCAC[A/G]AGGTCAGGAGATCGA	54476
rs536597595	snp	C/T	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5749216	AGTGCAGTGGCGTGA[C/T]CTTGGCTCACTGCAA	54476
rs536632882	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5723377	CAATTGGCCGGGTGC[A/G]GTGGCTCAAGCCTGT	54476
rs536645360	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5733510	AATATACTCAATTTC[C/T]ATGAGGTTAAACTGT	54476
rs536649498	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5659811	CCAAGCCTGGCAGGG[A/G]CAGGAAAGGCTAACC	54476
rs536653948	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5721853	ATGAGAATAAAAGAG[A/G]GCAGAATAACAAATA	54476
rs536666959	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5757348	TCATTATGAACTCTA[C/T]CAATGCTTCTGGCTG	54476
rs536678327	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5734035	TTAGAAACCCAAAAA[G/T]AAAGTATTTTAAAAG	54476
rs536687780	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5654439	GGTGCCTCATTCCAG[C/T]ACTTTGGGAGGCCAA	54476
rs536708179	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5660228	AAACTGTTGGGATTA[G/T]AAATATGAGCCACAG	54476
rs536708555	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5655133	GAAGAAACCCCATTT[C/T]TGAGATGAGGCACAG	54476
rs536715821	snp	A/G			missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741229	TCATGCTGAAACAAC[A/G]AGCGGCCCAGTTCTG	54476
rs536771466	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5729760	AAAACGGTGGCTCAG[A/G]GAGGTTAAACAAACC	54476
rs536785701	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5758512	TTTTCTTCCACTTGT[A/G]TCACTCCTGAGACAG	54476
rs536788537	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680745	GGCACCCCAGACAAA[A/G]GATGTCTGAAGCACC	54476
rs536794368	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5747843	AAGTATAGTGGCACA[A/G]TCATAGCTCACTACA	54476
rs536794545	snp	A/C/T	0.000528519	0.0162477	missense, upstream-variant-2KB	RNF216	GRCh38.p7	7:5752964	GTGATGGGCCCATCT[A/C/T]GGAGATTGATCCACT	54476
rs536817032	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5656635	TTCTTCACGTCATCA[C/T]GGAGGTTGCTGGTTA	54476
rs536825625	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782089	GGGCACAGTGGCTCA[C/T]GCCTGTAATCCCAGC	54476
rs536842706	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663208	TTTCCAAATGCCAGG[C/T]GCTCCTTGCGGCAAA	54476
rs536850029	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678513	GGAAAATGGCTCTGG[A/G]CCCGCCTGAGTAGTC	54476
rs536878973	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5732472	AAAACATGTTTGAGA[A/G]GTTCATCTCTCCCCA	54476
rs536888234	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5714447	ATTTTTAGTAGAGAT[A/G]GGGTTTCTCCATGTT	54476
rs536889853	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5627490	CGGTGGTTCACGCCT[G/T]TAACCCCAGCACTTT	54476
rs536913655	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5658372	TTAAATAAAATTATT[A/T]TGGGCCGGGCACAGT	54476
rs536921935	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676547	TCACAGTCTCCCGTC[C/T]GTCCTGTCTGCCTGG	54476
rs536925510	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5742654	AGGCTGGAGTGCAAT[A/G]GCATGATCTCAGCTC	54476
rs536930200	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5633683	TGAGCTCAGCAGGGC[G/T]CAGAAAGAACTCAGC	54476
rs536935794	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5658072	GCAGGGGAGCATGCA[C/T]GTGCATGCAGAGGAG	54476
rs536941201	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5761862	AGACATGGGAAATCA[C/T]CTTATACATTGCTGG	54476
rs536947715	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5691147	ACCGTGTGTGTAGAC[A/C/G]GTGAGCCTGGGTGAT	54476
rs536966474	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5704223	CGTCTTATATTAATA[A/C]GTTTATATTAATGCC	54476
rs536968088	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5732895	CAACCCTTAGATAGT[C/T]GTTGCTGCCTTCATC	54476
rs536968759	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5634044	GATATGAACAGTAAT[C/T]AGCAGCCACAGGCTG	54476
rs536978443	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670341	CACAGTGCTGCTGCC[C/T]GACTGCAGAGGACCC	54476
rs536985754	snp	C/G	0.0112339	0.0740996	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739572	GATCTGGTTCTCTGT[C/G]CCCATTTTACAGATC	54476
rs537001691	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5623263	AGGGCAGCGACCTCT[C/G]GACACGGGAGTGGCT	54476
rs537031932	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5746639	AGCCAACGTCATCCC[A/G]GTCCTGAGATATACA	54476
rs537032293	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5717803	TTAAATTATTTATGA[A/G]ACAGAGTCTCACTTT	54476
rs537043431	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5728659	ACAGTCCTTGGCTTG[A/G]TTCTTCCCTTCCTAC	54476
rs537073403	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643061	GCACTGACATGAAAT[A/T]ATAATGGGTATGGAG	54476
rs537112553	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5637710	ACCCCTGGATAACTT[C/T]GGGATTTTTTGTAGA	54476
rs537123843	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5649639	AAAAAAAACACATCA[A/C]CAGATTCCTTTGGGC	54476
rs537148906	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622232	GAAAGTTAGGCGGCA[A/G]CAGAACAAAACCCCC	54476
rs537151388	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5638026	TGCGCAGCAGCCCCC[G/T]TGGATGGGCCCCACA	54476
rs537151955	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5632755	GCATTCCAGCCTGGG[C/T]GACAAGAGCAAAACT	54476
rs537155674	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736523	AGTGCCGAGATTTCA[C/G]CCTCTGCCCGGCCGC	54476
rs537162581	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5644088	TAGTTTATTCATGAG[G/T]TGATGGATTGAGTTT	54476
rs537177667	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676482	CTGGGGAACCCCACC[A/G]AGCTGCACCTGCATT	54476
rs537209778	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5771503	ATGTTAACTGAAAAG[A/T]AAAAGAATCCCGGCG	54476
rs537251498	snp	A/T	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663591	TCCACCTCAGGAAAA[A/T]AAAAAAAAAAAAAAA	54476
rs537280978	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5702411	TTTATTCATATTGGC[A/G]TTTTGTTATAATGCG	54476
rs537283973	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5652798	CTGTCCCTTAAAAAA[A/C]AGACAAAGAGTTGGG	54476
rs537291415	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5633019	GAGTCGTGCTCTATC[A/G]CCCAGGCTGGAGTGC	54476
rs537320183	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713305	GCCTCTAGTTCCTAC[C/T]CGCTTCAGAAGGAAT	54476
rs537330263	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712460	CCTGGGCGACAGAGC[A/G]AGAATCCACCTCAAA	54476
rs537338409	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5766759	AACACATATAGCACA[C/G]AAAATAATGAAACAG	54476
rs537342373	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5696271	AAAACATGTTGCAAA[A/G]GGAGAATTAAGCAAT	54476
rs537344110	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5649849	ACCAGAACAAACAGC[C/T]CCTGGCAACTGGTAT	54476
rs537352806	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5697017	GGGTAGGGGAAGTCT[C/G]CAAAATAAAATCCAC	54476
rs537360243	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5642489	AAAAGTGCTGGGATT[A/G]CAAGTGTGAGCCACT	54476
rs537393417	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5710745	CCACTCCACTCCCAC[A/C]CTTTCCATCCTTTGG	54476
rs537398446	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5731539	ACCCAACACATGTTA[A/C]CTATCCAGGCTCTTC	54476
rs537409750	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5660182	GCTCTCAAATTTCTG[C/G]GCTCAAGCGATCTGC	54476
rs537432406	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667468	CTAGTTACCCTGGAG[A/G]TGACTCTGCTGATAA	54476
rs537435295	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5773277	AGACAGAGTCTCCCA[C/T]TGTCACCTGGGCTGG	54476
rs537441235	snp	A/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5648619	CATAGTCCCAGCTAC[A/T]CGGGAGGCTGAGGCA	54476
rs537446565	snp	G/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781210	GGCCTCGGGCCCGGG[G/T]GAGGGAAGCGCGGTC	54476
rs537452213	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5770630	TAGATATATACTAGA[C/T]GACTTTAGAATTTAC	54476
rs537460231	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674113	CGGCTCACTGCAACC[C/T]CCGCCTCCTGGGTTC	54476
rs537470705	snp	A/G	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5686935	GGCAGAGCTCAGGTC[A/G]TAATGCTCACTCACT	54476
rs537476951	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5634731	GTGGCCATGTTTTGC[A/G]TCCCGTCAGGGTCAA	54476
rs537481777	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5648541	CCATCCTGGTTAACA[C/T]GGTGAAACCCCGTCT	54476
rs537483120	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5700455	CATCTCTCCCTTGAT[A/G]AGGCCACAGACACAG	54476
rs537484574	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5775647	GGCCGAGGTGAGTGG[A/G]TTATTTGAGGTCAGG	54476
rs537494158	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780774	GATCTAAGTACCTAG[A/G]ACAGCTGCTACCCAG	54476
rs537495561	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5771940	AGAGAAATGTAAACT[A/G]AAACCACAAGGGGCC	54476
rs537506293	in-del	-/CA	0.0130921	0.0798413	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620703	CCTTAGGAGAAACAT[-/CA]CTCTGGGCTCCCCCT	54476
rs537522799	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5747056	ACTCCTACTGCTCCC[A/G]TTTTACCTGAATACT	54476
rs537523804	snp	A/C	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5771053	CCTTGTGATTCGCCC[A/C]CCTTGGCCTCCCAAA	54476
rs537524320	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5626259	CATAATCACTAAGTG[A/G]GTCAACATGAAGGAC	54476
rs537546408	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5701112	GGAGCACACACACGA[C/G]AGCCTCCCCCAGCAC	54476
rs537549680	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669222	AGTTGCATCTGACAA[C/G]ATCTCTGATTCCGAC	54476
rs537558632	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5695163	TCCACGGTTCTTCAT[C/G]TGTACAACAAGCATG	54476
rs537572545	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674761	GTGGCTCTAGGAGGC[C/T]GAGGTTGGCAGATCA	54476
rs537574846	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5731534	CCCAGACCCAACACA[C/T]GTTAACTATCCAGGC	54476
rs537576821	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5760550	CAAAACAAAACTGTA[A/G]AACAAAAAAATACAT	54476
rs537604748	snp	A/G	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5684204	ACCTTCCAGGTTCAC[A/G]CCATTCTCCCACCTC	54476
rs537632367	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5646674	CTCCAGCCTGGCGAC[A/G]GAGCGAGACTCCATC	54476
rs537661728	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5755606	TCTTTCTTGCAAATA[A/G]TGTTTGAGATACATC	54476
rs537685554	snp	C/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5779207	CTCTCTCAACTATCC[C/T]ATTCATCAACTTTCG	54476
rs537701363	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5756108	CCCCATTCTGCTCTC[A/G]TGATAGTGAGTGAGT	54476
rs537703170	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750822	AATTTCACCATCAGT[A/G]GTAGCCTCTGCAGAT	54476
rs537710575	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711693	GTAAACAGCAGATAT[C/T]TGGGCCATGAGGGCA	54476
rs537736880	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5711076	CAGTGTTCAACTCTA[A/G]TCATGCAATTTTAGA	54476
rs537770516	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5756331	TTTCTTCCTAGCAGT[A/G]TGAAAGCAGACTAAT	54476
rs537775421	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5706473	CATTTAAGTGGAATC[A/G]TGCAGTATCTGTCCT	54476
rs537775688	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5708022	GGGAGCCACCATGCC[C/T]GGACAGTGTGTTTAG	54476
rs537780790	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679068	TACAGAGATTAGATA[C/T]AGTGGAATGAATAAC	54476
rs537790645	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5685510	AAACATTACAACTTT[C/G]AAAACAGCAAGCTAC	54476
rs537822157	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5710366	CCTGCCTCAAAACTT[-/A]AAAAACAAAAACAAA	54476
rs537822331	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5694004	CACAAGCAAAGAACA[C/T]GAGAGAAGCACAGTG	54476
rs537835165	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5740329	GACAGGGTTTCACCG[C/T]GTTAGCCAGGATGGT	54476
rs537835282	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5735682	GGGAGAAGAGTTACA[G/T]AAGACAGGAAACAGC	54476
rs537837124	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5779826	ACAGCCAGACTCCGC[C/T]TCAAAAAAAAAAAAA	54476
rs537839918	in-del	-/A	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5637090	TCATAGCTCCAGCTG[-/A]AAAAAAAAATCTATT	54476
rs537850058	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668108	TTTGTGGATATCAGA[C/T]AGGACATCTTGCAAG	54476
rs537860887	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656239	GTGCCACTGCACTCC[A/G]GCCTGGGCGGCAGAG	54476
rs537866117	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5731158	TAAGAAAAGCAGCTA[C/T]TCTTTGTCGAGAAAA	54476
rs537872052	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736075	TCTAGCCTAGGTGAC[A/G]GAGTGAGACTCCGTC	54476
rs537873129	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5759236	GAGGCCGCTATGTTT[A/C]CTATACAGCCTACAG	54476
rs537882825	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5706891	TTCTTCTAGTTTTTA[C/T]AGTTTCAGGTCTTAC	54476
rs537904828	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662582	TGAAAGGAATGAAGA[C/T]ACTCTCATGTTCCCA	54476
rs537909935	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754491	TTTTAAGGATGAGGA[C/G]TTGCCAAGCTCCTCA	54476
rs537921598	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5632170	TTTGAGATCTGAGTT[C/T]CTGTTCATGCCATTT	54476
rs537934280	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5705745	GAAACCCCGCCTCTA[C/T]AAAAATACAACATTA	54476
rs537937977	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5655243	CCCTCTACGTCACAG[G/T]GCTTCTTCTGTAGGT	54476
rs537964276	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5626780	TCCTGAGTATCCCTG[C/T]GTCCAGGAAGCTCAT	54476
rs537989909	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5683559	TCAGAACTCTCTGAA[C/G]AGGTAAGATGTTCTC	54476
rs537996633	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5702288	AAGGCGGGCCAAGGG[A/C/G]AGAGGCAGGTGCTTC	54476
rs537996844	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754859	ATGGTAAAACCCCAT[C/T]TCTACTACAAATACA	54476
rs538014003	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671527	AGGACAGAGAGAGCC[A/G]GGCACGGTGGCTCAC	54476
rs538020227	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5715520	TGCTAATGTGATTAT[A/C]AACAGCAAGGATAAG	54476
rs538020525	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5721807	AGGGGCTGAAGGAAC[A/G]GTACCTAGATTCACC	54476
rs538022560	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5716272	CCCAGCACTTTGGGA[A/G]GTTGAGATGGGTGGA	54476
rs538025967	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5744843	TGGGAGTGGTAGCGC[A/G]TGCCTGTAATCCCAG	54476
rs538039423	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665696	AGGGTAAAGTCTTTC[C/T]GGAATAAATCAAAGT	54476
rs538062801	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672090	TGGCAGTGGATCAGA[A/G]AAGTTCCCGCCCCTT	54476
rs538078680	snp	A/C	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666177	TCTCAAAAAAAAAAA[A/C]AAAAAAAATCCGAAA	54476
rs538083854	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5716561	AGAGTGACTATACTA[C/G]ATCACGTATCTGACT	54476
rs538091796	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5711258	ACAGCTCTGCTCCCA[C/T]GTAATATAGTCAGTT	54476
rs538137315	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5636567	GAACAGGCTTGTGTG[A/G]CAGTGCATGCTTTGT	54476
rs538145121	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5739895	GTGATCCCAGCTACT[C/T]GGGAGGCAGAGACAG	54476
rs538147828	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5661522	AAAAAAGTAAATACG[A/G]CTGGGCATGGTGGTT	54476
rs538154232	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5769250	AGCCTCCCGAGTAGC[G/T]GGGACTACAGGCGTG	54476
rs538165489	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781544	GCCGACACTCACTCG[C/T]CACTCAAGTCGCCGG	54476
rs538183650	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5758904	GTGAGAAGGACAAGA[A/G]ACTTGGGAGGGGCTG	54476
rs538193398	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620526	GCCTGGAGAACCAGG[C/G]TGGGTGCTCACGGCA	54476
rs538193501	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5625427	GGTTGGAATATTAAT[A/G]ATGATCAGTTTGGAT	54476
rs538204690	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5688487	ATGTGCTAAGAAATA[C/G]AGAAGTTATTATAAA	54476
rs538215054	snp	A/C			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669887	AGACTCCATCTCAAA[A/C]AAAAAGAAAGTAAGT	54476
rs538225306	snp	A/G			intron-variant, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711362	AATCAAAGAAGCGTC[A/G]TTTGGACTTTGAAAA	54476
rs538237476	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5714548	CAGGCGTGAGCCACC[C/T]GGGCAAAAAGTCATC	54476
rs538237688	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5655898	GTCTCACTCTGTCAC[C/T]CTGGCTGGAGTGCTG	54476
rs538241273	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5650600	TGGCTGTCAGCTGAG[G/T]GTTTTCCCAACTTCT	54476
rs538275424	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5645475	ATAATTTCAACAGCC[A/G]TATCTTCAAGATCTC	54476
rs538275874	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5689500	TGGAGGCCATTTTCT[-/A]AAAAAAAAACAAAAA	54476
rs538310570	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5639808	TCTGTCGCCCAGGCT[G/T]GAGTGCAGTGGCATG	54476
rs538317208	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5715538	CAGCAAGGATAAGGA[A/G]TATGAGAGATGTTAC	54476
rs538321138	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5749122	TTTGGAAAACAGCTG[C/T]GTTCTGATCAGCAAA	54476
rs538328388	snp	C/G/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5632733	AGTGAGCCAAGATCA[C/G/T]GCGACTGCATTCCAG	54476
rs538351274	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5640188	CAGGCGTGAGCTACT[A/G]TGCCTGACCCTCTCC	54476
rs538353470	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5738433	AAGAAATATGGCTGG[C/G]AGCGGTGGCTCACAC	54476
rs538381014	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5749966	TTTTCTTTTAAGGTT[A/G]TTATAGCTTATAGCA	54476
rs538396947	snp	G/T	0.0517044	0.152246	intron-variant	RNF216	GRCh38.p7	7:5707720	GTGTGTGTGTGTGGT[G/T]TTTTTTTTTTTTTTT	54476
rs538402651	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5643029	GGGTCTATTTGCTTG[C/T]TCATCCGATCTGTCT	54476
rs538406139	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5773065	GATTACAGGCATGAG[A/C]CACCATGCCTGGCCC	54476
rs538409742	snp	C/G			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620518	ACAGAGGGGCCTGGA[C/G]AACCAGGGTGGGTGC	54476
rs538455471	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5724200	TCAAAGAGACCCTGA[A/C]AAGCTAGAGAAGGGC	54476
rs538464685	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5729682	GAATTACATGTGTAG[A/G]AAAGAATAACATTTG	54476
rs538473318	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5705458	GTTCTCCAACTCCAA[C/G]GGCAGTTATGGTCCT	54476
rs538476241	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5630001	CAGGCATATGAGCAT[C/T]ACCATCCTGTGAAGA	54476
rs538516349	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5724877	GTTTTCAGCAGTTAT[C/T]TCATCAATAAGAATG	54476
rs538529570	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5763749	TGAATTTTTAAAATT[G/T]TTTTGTAGAGACAGG	54476
rs538530144	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5655376	GCCGAGGCGGAGGGA[A/T]CACCTGAGGTCAGAC	54476
rs538534972	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5698933	GGACATTCGAATAAG[A/G]GTCTTTCCAGTCCCC	54476
rs538538358	snp	C/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5692781	TATTTTTCAAGTTCT[C/G]TTAATACAAACAAAA	54476
rs538547165	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5699760	GCTGGGTGGTTGATT[C/T]CACTTGCAGTGATGT	54476
rs538562239	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5730186	ACTTAGAGGGAAGTG[C/T]ACTCATGTTTTTGCA	54476
rs538575123	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782351	GCAACCCTCCATCTC[A/G]AAAAAAAAAAAAAGT	54476
rs538582593	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619986	ACCCAATCACTTGGA[C/T]GAATCTGTCGGCGGC	54476
rs538584244	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782710	CAAAAATTAGCTGGG[C/T]ATGGTGGTGCGTGCC	54476
rs538584477	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5691372	TTCCTGTTCTGGCTG[C/G]ATTGCTCCTGGCTGG	54476
rs538645433	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676390	AACACAAAACAAAGC[G/T]GCCCTTAAAAGTGCT	54476
rs538672134	snp	A/G	1.71979e-05	0.00293235	intron-variant	RNF216	GRCh38.p7	7:5715002	CAACATGGTCTCCTT[A/G]GACTCCAGGAATGTG	54476
rs538679388	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5777744	ATTATGGATATAAAT[A/G]TGCAAACAATTAGTC	54476
rs538686992	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5732958	CTAAGTTAACCAGCC[A/G]AAGTAGATTACCTGC	54476
rs538688194	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5710176	ACCAGCCTGGCCAAC[A/G]TGGTGAAACCTCATC	54476
rs538698028	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5743479	TACTCTACAACTGAC[C/T]CCTACCAAAAAAAGA	54476
rs538708437	snp	C/T	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5690781	CCACACTAGAGCTCA[C/T]GCCCCGACAGCCTGC	54476
rs538713606	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5778209	CATACCTTTTCCCCC[C/T]GCATTCACCATTCAG	54476
rs538715732	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5772677	CAACTTATAGAATGT[G/T]AAGTTATAGATACTA	54476
rs538723305	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5628543	TTTCCTTTTCTTTGA[A/G]ACAGTGTCTTGCTCT	54476
rs538728654	snp	A/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5634665	GCCCAGCACCCAAAT[A/G]CCACTATCTGGAGCA	54476
rs538736689	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5633905	CATCCTCCCTTAGCT[C/T]GTCCCTCCACAAATA	54476
rs538743713	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5703953	ATTCCAGAAGCATCA[C/G]CTTCAAATCTCCTTT	54476
rs538753759	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5697189	TAAAGTTCTCCCCAT[C/G]TCCGCCAATAAGACC	54476
rs538754902	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670962	AGGAGGCCTAGAGTG[C/T]TTTCTGTGAACTGCT	54476
rs538760651	snp	A/T	0.00557542	0.0525036	intron-variant	RNF216	GRCh38.p7	7:5623481	TTTTTTTTTTTTTTT[A/T]AATAGATGGGGTTTT	54476
rs538761751	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5704830	TTTCACTTTATTTTC[C/T]ATGATGGGCCAAACA	54476
rs538780764	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5776760	ACAAAAATTAGCTGG[A/G]TGTGGTGGCTCATGC	54476
rs538793663	in-del	-/G	0.000379416	0.0137682	intron-variant	RNF216	GRCh38.p7	7:5729413	GGTGTGACCCCAACA[-/G]GAAGACCAAGTAGAG	54476
rs538799144	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781022	GGTTTGACGCACTTG[C/T]GGCGCCCTCGCGAGT	54476
rs538816453	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5686415	TCCCCATTTCTCTGA[C/T]GAGGAAAGTCAGAGT	54476
rs538818481	snp	A/T	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5680326	CATCATAGAATGCGA[A/T]CCACTCCCCCAAGCC	54476
rs538822751	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5729186	CACTCCTGCATTCCA[C/T]AGTAGAAGGTATTAC	54476
rs538836463	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5747259	GGGGAAGACTTTCAG[A/T]CATTTTTTAAAGAAT	54476
rs538837313	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5655092	CTGGCAATTCCGTTA[C/T]TAATTCATGGGTCTT	54476
rs538844623	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5718637	CTGCAACCAACCTCG[A/G]CCTCCCATGTTCAAG	54476
rs538858285	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5757928	GTGAGGCAGAGGCAA[C/T]TGGATCACTTGAGCC	54476
rs538865895	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5650914	CAAATTGCCATTGCC[C/G]ACTTCATTTTCTGAG	54476
rs538886008	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5776311	GACTATAGCCGGGCA[C/T]GGTGGCTCAAGCCTG	54476
rs538897588	in-del	-/CT	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5637505	GGTTACCACAGAGGA[-/CT]CACATCTTTTCAAAA	54476
rs538904484	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5708502	ATTCAGTAGAAACTG[C/T]AATTCAAGTACCCAT	54476
rs538931508	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680712	CAGCACTCAACACTT[C/G]TACTTGGATATCTAA	54476
rs538932518	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5638211	AATCTTCCTGTTTCT[C/T]TTCTTCCATGTTTTA	54476
rs538941920	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5760705	ACTCCTTTATAATCA[C/T]CACGCCTTCAAAAAC	54476
rs538947257	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674774	GCCGAGGTTGGCAGA[C/T]CACCTGAGATCAGGA	54476
rs538966561	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5708983	CTCTTGTTCTCAGCA[G/T]CCCCCAGGGACCTAG	54476
rs538978174	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681634	CTTGCTTAGGAAGTG[A/T]CAAGGACGAGTCCCA	54476
rs538982143	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753453	TAAGAATCATTTAAG[C/G]AAACCTATGTCAATG	54476
rs538985141	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669832	GGGAGGTGGAGATAA[C/G]ATCGAGCTGAGATCG	54476
rs539031036	snp	A/G/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5770457	CGAGAGCAAAACTCC[A/G/T]TCTCAAAAAAAAAAA	54476
rs539057877	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664364	TTGCTCCCTAATGTC[C/T]TTCCCCAATTTAATG	54476
rs539061388	snp	C/G	0.00557542	0.0525036	intron-variant	RNF216	GRCh38.p7	7:5657849	ATAAAGTTCAGCAAA[C/G]TCAAAGCTCAGGTAG	54476
rs539065329	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5633646	CAGGGAGGGAGATTT[A/G]TTTCCTTTCCTTGAA	54476
rs539068852	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5756296	ACCTCTTTCCGTCAT[A/C]AATTACCCAGTCTCA	54476
rs539091824	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5759922	AGGAGTGAGCCACCA[A/C]GCCTGGCCTGGGGGA	54476
rs539130280	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5697527	TCTTCTGTACCATGG[C/G]TGGGCTAAGGCTTTT	54476
rs539131665	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5762364	CCCATCTCTATTAAA[A/C]ACACACACACAGGCT	54476
rs539134361	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767581	AGCAGAAATCTCAGC[A/G]AACATGTATTGTTGA	54476
rs539141012	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5733413	AAGGTATCAATTTGA[C/T]TACGTTTTAGTGATT	54476
rs539172320	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664958	CCCGCCACCAGGCCT[A/G]GCTAATTTTTGTATT	54476
rs539172929	in-del	-/TTTT	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668225	AATAGCAAAGCGGAC[-/TTTT]TTTTTTTTTTTTGAG	54476
rs539199283	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5751967	CTGAGGGGGGCGGAT[C/T]ACGAGGTCAGGAGTT	54476
rs539208380	snp	C/G	0.00438332	0.0466095	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668294	AGTGGCGCAATCTTG[C/G]CTCACTGCAAGCTCC	54476
rs539216178	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5686192	CATGCTGCTGCACTC[C/T]AGCCTGGGTTGACAG	54476
rs539221254	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5723645	GAGCAAGACTCCGTC[C/T]CAAAAAAAAAAAATA	54476
rs539225778	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5649200	CAGCTTGGCCAACCA[C/T]GGCCGACAAAGTAAA	54476
rs539241101	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5740891	ACGCATACCAACAAC[C/T]TTTTTTTTTGCAATG	54476
rs539257689	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5771042	CGAACTCTTGACCTT[G/T]TGATTCGCCCACCTT	54476
rs539258454	snp	A/G	0.00159617	0.0282053	utr-variant-5-prime, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781664	TTCCGGCCCTGCCGC[A/G]GCGTCACCTCGCGCC	54476
rs539264946	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5649603	GGCAAGTTGAAGCCC[A/G]TGGAGCACCCTCTCT	54476
rs539270518	snp	A/G	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5719333	GTAAGCCATGATTGC[A/G]TCACTGCACTCCAGC	54476
rs539273502	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668836	GGGCGTTCTAGTCAC[A/G]GTGTATCTTCCCCAT	54476
rs539283385	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736503	CGCCTGCCTTGGCCT[C/T]CCAAAGTGCCGAGAT	54476
rs539286032	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5747543	AAAGCAAAATAGATG[C/T]CCCTTTATAAACTAA	54476
rs539295809	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5632371	TGCTCTCCTTCTGGC[C/T]CCTCCTAATCCCAGT	54476
rs539324691	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5638751	CAAATGATCCTCCTG[C/T]CTCAGCCTCCCAAGT	54476
rs539344552	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5742128	CTCGGCTCACTGCAA[C/T]CTCTGCCTCCCGGGC	54476
rs539357522	snp	A/G	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5639564	CGCCTCCTGGGTTCA[A/G]GCAATTCTTTCTCAG	54476
rs539359706	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5695573	GACACCGCAGCTATA[A/G]ACAAGTTCTATTGCC	54476
rs539371744	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5732357	ACACGGACTAGCTTT[A/C]AAATGGTCTGTTTTT	54476
rs539384860	snp	A/C	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5761283	TCAAAAAAAAAAAAA[A/C]CCACACAAACTCAAA	54476
rs539385520	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5719507	GAGACTACAGGGGTC[A/G]GGTTAAGAGAGACTA	54476
rs539389091	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5773295	TCACCTGGGCTGGAG[C/T]GCAGTGGTGCAATCT	54476
rs539392925	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622293	TGAGTAGGTGTAAGA[A/G]GGGAGGAGAGGTGCC	54476
rs539431271	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750781	TTACTTATGCCTCTC[A/G]CGTGGCAGGACAACG	54476
rs539432195	snp	A/C/T	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5722491	GCCCCCCGGGGTTCA[A/C/T]GCCATTCTCCTGCCT	54476
rs539439993	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5647190	TCTGGTGGGAGATAG[G/T]AGTTTTTGGAATTCC	54476
rs539449099	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5696168	AGTCCATGTGGTGAC[A/G]AAGAGCAGTTGGTAC	54476
rs539465416	in-del	-/A	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5699050	GTTTTTTTTAAAACT[-/A]AACTTTTTATTGTAG	54476
rs539466964	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5644090	GTTTATTCATGAGTT[A/G]ATGGATTGAGTTTTT	54476
rs539507087	snp	A/G	0.00557542	0.0525036	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712252	TGGGAGGCTGAGGTG[A/G]GTGGATCATTTGAGG	54476
rs539514186	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5691079	AGAACTCTGTTCTCA[C/T]GGGTTGATCTGCCAT	54476
rs539536726	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5641477	TAAAATGATCACTTA[C/T]GGCTTTTTTGTGACA	54476
rs539544908	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664092	TTTGAGCGGCACAAG[A/G]TGCTGAATGTCTGAG	54476
rs539551402	snp	A/G	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5642977	AAGAGGCTGTAAAGA[A/G]TTAAGGTTACAGTCT	54476
rs539554483	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5637134	TGAAGTTCCTAGAGA[C/T]GGTTGCCTCCCACTG	54476
rs539584047	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5770741	TTAAGTTACACTAAT[C/T]AAGACAATATTGTAT	54476
rs539608104	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5775622	CACCTGTAATCCCAA[A/C]ACTTTGAGAGGCCGA	54476
rs539654686	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5726337	ATCACATGACAATGG[A/G]CTGGTGAGTCCCATT	54476
rs539655185	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656782	CTGAATAATGATTAA[A/C/T]GAATAAAGCAGAAGA	54476
rs539664155	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5710591	AAGTAGACTTTCCTT[A/G]TATTTTATCTCTCCC	54476
rs539671341	in-del	-/ACTG	0.0142736	0.0832652	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677629	CTCAGATTGGAAAGA[-/ACTG]ACTAAGAACAGGTCT	54476
rs539675553	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5694648	GAGGCCCACTTGTGG[C/T]GCAATTTGAGGACCT	54476
rs539715299	snp	C/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652131	CTAAGTTAATTAAAA[C/T]GCGTTACTTGCTTAT	54476
rs539718326	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5726694	AAAACCCCGTCTCTA[C/G]TAAAAATACAAAAAA	54476
rs539720007	snp	C/G	0	0	intron-variant	RNF216	GRCh38.p7	7:5721943	GATTTTCTTTTTGGA[C/G]ACAGAGCCTTGCTCT	54476
rs539740015	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5701663	AGCTAGAATTAAAGC[A/G]TAAGTGGGTTTAATA	54476
rs539747100	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5766111	CAATATAGCTAGACC[C/T]TGTCTCTACGAAAAA	54476
rs539759851	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5627456	AGGGGCAATTTCATA[A/G]CATTAAAGACTAGAC	54476
rs539780177	in-del	-/C	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5771794	GGAGTGAAACCCTGT[-/C]CCCCCCACCAAAAAA	54476
rs539783882	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5755557	TTTCTAATTGCGCAG[A/G]TAAGTTTTGCATGTT	54476
rs539791977	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678441	CTCCCCAAGCGCAGA[C/G]AAAAATGAGATTCAG	54476
rs539803433	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5652782	GCAACAGAGTGAGAC[C/T]CTGTCCCTTAAAAAA	54476
rs539814208	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5684896	GGTGCTTGGGAGTCC[G/T]GCATGGGGGGCTGGG	54476
rs539821997	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5768989	AAATCCACACATTAA[C/T]GAAGAAATTACAATG	54476
rs539841069	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666486	GAGCAGGGTGGGCAG[A/G]GCTGTAAGGTGGAGA	54476
rs539871431	snp	G/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5660952	CCTTAGGTTTTTTTT[G/T]TTTTTTTTTTTTTTT	54476
rs539882737	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5630723	AGCGCCAAGCACAGT[A/G]ACAACAACAGTAGTT	54476
rs539917200	snp	G/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5775026	GGTGAGATTACAGTC[G/T]TAAGTCACTGTGCCT	54476
rs539924385	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5651529	GAGCTACCCTGCCCG[C/G]CTGTGAGACAATCTC	54476
rs539945700	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5693508	TTTAATGCTAAGAAG[C/T]TCCAAGACATTTGAG	54476
rs539961313	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5707023	ACAGAGCACCATTAA[C/T]CAGAGACTACCTTTT	54476
rs539966727	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679390	GGCAAGCTGTGGTCC[A/G]GCCAGCCTCACAAGG	54476
rs539971578	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5658036	ATAATGGGGGTTCAG[C/T]GTAATGTGCACGCAC	54476
rs539983043	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5621054	GGGCGCCAGCAAGGA[C/T]ATAGCAGCAGGCTGC	54476
rs539988326	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5730108	ATAGTATACGCTGTA[C/T]ACAAATCTCACATCA	54476
rs540022733	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676464	CATCTGTGAGAACTG[C/T]CGCTGGGGAACCCCA	54476
rs540032535	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216, RNF216-IT1	GRCh38.p7	7:5661934	TTACTCTAGTCCCAC[C/T]GTGTGCCCACATGGC	54476
rs540053050	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5760048	TCTTCCATGGAATTT[A/G]TAATTGCAAAAAATG	54476
rs540056825	in-del	-/C	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5736686	TGAGGAGCGTCTCTG[-/C]CGGGCCACCCATCAT	54476
rs540085374	snp	A/G	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5639894	CCTCCTGAGTAGCTG[A/G]GACTACAGGCGCCTG	54476
rs540088306	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5760488	GCCATTGCACTCTGG[C/T]CTGGGCAATGAGTAA	54476
rs540107701	snp	C/G/T			intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739477	GGCTGTGAAGCAGGT[C/G/T]TGTGTGTGTCTTCAA	54476
rs540122721	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5634831	CTGGACTGTGCTGCC[C/G]TGCTTGGGAAAGCCC	54476
rs540128784	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5718798	GTGATCTGCCCACCT[C/T]GGCCTTCCAAAGCAT	54476
rs540132861	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5773187	TGGTATTTAAAAGAA[A/C]AGCTCTGGTATCAAA	54476
rs540144269	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5684389	TGGGATTACAGGTGC[A/G]AGCCACTGCGCCTGG	54476
rs540161530	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5739076	GGGGATGGGGAGTGA[A/G]TGTTTAATGCGGACA	54476
rs540163304	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621573	GCTTCAGGAGGTGGC[A/G]GGCCACTCCGGAGAC	54476
rs540169832	snp	A/G	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5736987	TCTGGGAAGTGAGGA[A/G]CCCCTCTGCCCGGCC	54476
rs540183140	snp	A/G	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5625218	AGATAGCTGACTATA[A/G]GAGGGCTCTGTTCCC	54476
rs540187381	snp	C/G	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5660598	TTAATGATTGACTGA[C/G]ACAGGGTCTCACTGT	54476
rs540197096	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666452	GGGGGAAAGAATTCC[A/G]GGCACCAGGAACAGG	54476
rs540225419	snp	A/G	0.00159617	0.0282053	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619847	GGTAGCCGCCCTAGC[A/G]GGATTTGCCTAGCAG	54476
rs540244574	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5630907	TCTCGTCTCAAAGCC[G/T]GAGCTGTTAACCACA	54476
rs540246420	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5655691	GGCAAGCAAACACCA[A/G]GCTGGGGAGTTTAAC	54476
rs540256376	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782507	GGAGGATCGCTTGAG[A/G]CCAGGAGTTCAAGAC	54476
rs540265209	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5655174	GCAAAATGACCTGGC[C/G]AGGCTGGAGCCAGGT	54476
rs540283217	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5775745	GTGGTTGCAGGCACC[C/T]GTAGTCCCAGCTACT	54476
rs540299566	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620279	TTCCTCTCTCCAGTT[A/T]TAAGGCAAGTAAGAG	54476
rs540319329	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753766	CTTTGGGAGGCCGAG[C/G]TGGGTGGATCATGAG	54476
rs540335629	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5698246	CTGGTTGCAGCTGGA[C/T]TGCATGTAAGCAGTT	54476
rs540336087	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5688649	GAAGGCTCACTCTGC[A/G]CACCTTACCTTGCTT	54476
rs540341332	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5720672	CTCTGGGTCACACTT[C/T]GAGAGCCACTGGTTT	54476
rs540399692	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670686	CCTTTGGAAGCAAAA[C/G]TACAGCTAAGGTGGT	54476
rs540400567	in-del	-/AA	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5637775	GAACTCCTGAGACTC[-/AA]GAGATCTGCCCGCCT	54476
rs540409982	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5743654	TGTATATGTACCCAC[A/G]TGTATATACACATGG	54476
rs540416202	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5639462	TGAGCCACCACACAT[A/G]GCTCCACATTTTTTT	54476
rs540427561	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767727	CCTCAGCCTCCTGAG[G/T]AGTGGGGACTACAGG	54476
rs540450713	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5634366	GTTGTTAATAAACTT[G/T]CAATGATTTCATGAG	54476
rs540469701	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5765068	AAAGCAAGACTCTCT[C/T]AAAAAAAAAAAAAAA	54476
rs540481042	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5692074	TCCTACCCAGAGTTT[C/T]GCTGAAAAATAGAAT	54476
rs540496631	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5733597	AAGTTTATACTTTTC[G/T]CTATCATTTACATTT	54476
rs540524725	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5734280	TAGCAATGGAAAATA[C/T]ATAAACTGTGGTTCT	54476
rs540566052	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5773707	CTGAGTAGCTGGGAC[A/G]ACACATGCGTGCCAC	54476
rs540580950	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665961	CCGAGGTCAGGAGAT[C/T]GAGACGATCCTGGCT	54476
rs540592129	snp	G/T	3.78136e-05	0.00434803	intron-variant	RNF216	GRCh38.p7	7:5624156	TGAGAAGGATGAACC[G/T]GTAGCTTCATGCAGT	54476
rs540629056	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5724563	TGTCAGCAGAGCCAC[C/T]GCTCCACAGACTGGC	54476
rs540636071	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753136	TAAGCATTAAGAGCC[A/T]TGTTTCTATGCTGAC	54476
rs540695364	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5714658	CCCATACTGTGTTTG[C/T]TATGCTGGTGTCCAG	54476
rs540707987	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5771722	AGATCTCTTGAGCTC[A/G]AGAGGTGGAGGTTGC	54476
rs540713003	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669401	TATCCATTCTTTTCA[A/G]TGTGGCTGAAAAGAC	54476
rs540715672	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681838	CACCCAGAAAAGGAG[A/G]ATAGGAGGTGAAAAG	54476
rs540727334	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5702784	GTACTCAGACACAAG[C/T]AGAGTTAAAAATCCT	54476
rs540729108	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675951	TGACCTCAGATGATC[C/T]GCCCACCTCAGCCTT	54476
rs540739455	in-del	-/CTGAGTAG	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5648230	TCTTGCCTCAGCCTC[-/CTGAGTAG]CTGGCATTACAGGCA	54476
rs540739819	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5638912	AGCTTACAGACATGA[A/G]CCACTGCACCTGGCC	54476
rs540747003	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5627250	ATGGTCCTCCTGGAG[A/G]AAATCCACAGAAAAG	54476
rs540756092	snp	A/G	0.00478085	0.0486577	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675234	CACTTCACAGACATC[A/G]CCTCATTCAATTCTT	54476
rs540765907	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5695528	GTGCCTCTCCCTGCC[A/G]GTCTCCTGCTCTCTC	54476
rs540770942	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669943	ATCCTTTTTTTTTTT[C/T]TGAGATGGAGTCTCG	54476
rs540771329	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5742965	TTTGGCACTATTTAT[A/T]AAAATAAAAAACGTA	54476
rs540796894	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5709306	AAGATGCCAGGAGTT[A/G]GGAGCTTCCTCCCAA	54476
rs540800487	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5703416	GAGCTGCCCTGGCAT[C/T]GATAGCTGGTCCACA	54476
rs540810860	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5733105	TGCTCAACTCAGCTT[C/T]GGGCCTTATTTCCAG	54476
rs540811057	in-del	-/GGTAGATG	0.0111196	0.0737302	intron-variant	RNF216	GRCh38.p7	7:5735539	GAAAACCAGTAACAC[-/GGTAGATG]AGTTAAAAGGAGATT	54476
rs540824465	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5742832	AACTCCTGACCTCAG[A/G]TGACTGGCCCACCTC	54476
rs540851106	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5728982	ATTTTAGGATCCTGC[A/G]GGGAGAACGCTGGGA	54476
rs540875787	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5628807	GGATTACAGGCATGA[A/G]CCATCACACCCAGCT	54476
rs540884057	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5763447	ACTAGCCGGGCCAAC[G/T]TGGTGAAACCCATTT	54476
rs540923816	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643413	CCCCGCAGGATGTGC[C/T]CCCGGGGCAGGACAG	54476
rs540945511	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5778822	AATCTCGGATCACTG[A/C]AACCTCCGCCTCCCG	54476
rs540962308	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679936	AAGAAACACAATAGG[A/G]ACCCTGTATGCACAG	54476
rs540963300	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5723898	AAGGCTAAGTGTGAG[C/T]CATAAACATTAAACT	54476
rs540970966	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5747403	GAATATTATTTTCCT[A/G]AGGATGATATTCAGG	54476
rs540971686	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5655415	CCAGCCTGGCCAACA[C/T]GGAGAAACCCCATCT	54476
rs540988114	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RNF216	GRCh38.p7	7:5781784	GAGAGGGCCGCCTAG[C/T]CGCGCCTGCATCCGG	54476
rs540990723	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674928	CTTGAACCAGGGAGG[C/T]GGAGGTTGCAGTGAG	54476
rs541007959	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5707672	AGTGATATCCTTGCC[G/T]TGTTCCTGATCTTAG	54476
rs541021556	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5719107	GAAAGTTGGCAGGGC[A/G]TGGTGGTGCATGCCT	54476
rs541023740	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662801	GGCAGGCAGTGTGAA[C/T]AGGGAGGGTGCCATC	54476
rs541032814	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5686646	TAAATACATGTGAGC[C/T]GGGTTTGGAAGATTT	54476
rs541035194	snp	C/T			intron-variant, nc-transcript-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662435	AATACTTGCCACTTA[C/T]CTCCTCAAAGGTGGC	54476
rs541048170	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5701424	TAGGATCTCCGTTCA[C/T]CTCCTGAGGCCGCAC	54476
rs541050055	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5638406	CCAACTGTCTCCTGC[A/G]GATAACCTTTTCTAA	54476
rs541053905	snp	A/G	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5757577	AAGGAATGAGTTACT[A/G]ATATATGCAACAACA	54476
rs541058578	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5714058	CCAAGGCTGGAGTGC[A/C]GTGGTGCGATCTCAG	54476
rs541071382	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5632811	CCTCCAGTGCCCCAT[C/T]GCTACTCCAGAAGGT	54476
rs541073873	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5708622	AGATTTTGCTAAATC[A/G]TAGGCTAATATAAGT	54476
rs541094154	snp	A/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5633413	AAACCCCGTCTCTAC[A/T]AAAATACGAAAATTA	54476
rs541114007	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5627563	TCATCCTGGCTAACA[C/T]GGTGAAACCCTGTCT	54476
rs541115502	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5627185	TACCTTGTTCAATGT[C/T]ACGGCTAGTTGGCGG	54476
rs541137115	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5633761	GGGTGGGAGGAAGAC[A/G]CAGCAAGAGCTTGTG	54476
rs541145303	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5642268	CCTAGCCTGGGGCAC[A/T]GTGGCTCCATCTCAG	54476
rs541150598	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622055	CAGGGTGGCAGAAAC[A/G]TCTCCCCCAGCAGTT	54476
rs541152117	in-del	-/CTC	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5651871	CAGGATGGTCTCAAT[-/CTC]CTCCTGACCTCGTGA	54476
rs541165162	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5727591	AAAAAGATCATCCAG[C/G]TGTGGTGGCGTGCAC	54476
rs541178557	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5625297	GAGGGATGGTGGTCC[C/T]TGATATCGTGAGAGG	54476
rs541187676	snp	A/C	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5780046	GACTATTGCAGGAAG[A/C]TGGAGGACAAACAAC	54476
rs541191898	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5756555	TTCCAACACCATGCC[C/T]GGCTAATTTTTGTAT	54476
rs541260311	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5642131	TACCTTAATGAGTCA[C/T]CTCTGTAGTACATCC	54476
rs541292385	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5718853	TGAGCCATCCCACCC[A/G]GCCAAACTTAAGTTT	54476
rs541328422	snp	A/C	0.00795532	0.062565	intron-variant	RNF216	GRCh38.p7	7:5686277	TCCAAACTCTCAAGA[A/C]CACCACTGCTGCCAC	54476
rs541333502	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5632494	GTGTCCCTGGATCAG[C/G]AAGGGCTCAAAAGAA	54476
rs541347448	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5770826	TTTTTCTTTCCCCCC[A/G]AAACAGTGTCTTGCT	54476
rs541350942	snp	A/G	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781177	CGCGCTCGGGTGCAC[A/G]GACACCGCCTCCGCG	54476
rs541362628	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5736311	TTTTTTGGTGGAGAT[A/G]GGGTTTCGCTGTGTT	54476
rs541388787	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5771121	CCAGATTCAGTCTTA[C/T]ATGAATGTTTATGAC	54476
rs541395591	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668966	GGGCTCTTATCCAGC[C/T]GAAATCTAGTCATCT	54476
rs541403145	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5736562	CTGGGAAGTGAGGAG[C/T]GTCTCTGCCTGGCCG	54476
rs541428333	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5734458	TTTGGTTTGTGATAA[A/G]TTATTGAGCTGTGCA	54476
rs541437582	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663233	GGCAAAGATGACGTC[C/T]TGCTGGTCACTATGG	54476
rs541456191	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5701963	CACTAACCCAGGAAG[A/G]CAGCTCAGGACCAGA	54476
rs541459603	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5689720	CACTTTGGGGAGGCC[A/G]AGGCAGGTGGATCAC	54476
rs541470276	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5695803	CCTTGCTTTGCCTGT[A/C]AACGGATGTGTTTAT	54476
rs541479122	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5755229	AAAGGAAGGAAGGGA[C/G]GGAAGGATGAAAGGA	54476
rs541479817	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5695366	ACGCCAGCCTGTCCT[A/G]ACCTCACACTCCCCA	54476
rs541511109	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5701582	CGTTCTTATTGTACA[C/T]GGAAAGGAAATGTGG	54476
rs541517707	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5647413	ATCATGGCTTACTGC[A/G]GCCTCGAACTCCTGG	54476
rs541528475	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5761425	TTAACAGGCAATTCA[A/G]TTCACAAAAAAGAAA	54476
rs541545697	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5657912	AATCCAAGAACCTCT[A/G]TTTTTCCTAGGTCAA	54476
rs541558841	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5684455	TTAAAACAAATGCTG[A/G]TCTTTAGGCTCCTCT	54476
rs541565384	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5761927	GCAATTAGCAATACG[C/T]CCTAAATTACAAATG	54476
rs541588720	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679169	ACAGACTTTTCAGGA[G/T]GATCCTGTCACCCTC	54476
rs541603115	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5717555	AACAGGGAATGATGT[A/G]TGCACAAACTTATCA	54476
rs541612676	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673054	ATCCATCTCTCCATC[A/G]ACTCAGGGTGGTGGG	54476
rs541614360	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5746332	AATCACTGGCAATAA[C/T]TGTATTTTTTGCTCC	54476
rs541627092	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5764423	GAGGCTGAGGAGAGC[A/G]GATCACTTGAAGTCA	54476
rs541639007	snp	A/C	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5706229	CATCTCAAAAAAAAA[A/C]AAAAAAAAAATTGTG	54476
rs541679308	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5661725	TGAGAATCGTTCGAA[C/T]CTGGGAGGCAGAGGT	54476
rs541733286	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673560	GAAGAGAGCAAGTTG[C/T]AGGATCAAGTGCAGG	54476
rs541736618	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5694738	TTCTCTGTAGCTGCG[C/T]AGCTTGTGTTGGGCT	54476
rs541739119	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5715891	GGATTACAGGCACCC[A/G]CCACTATGCCCAGCT	54476
rs541746108	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5625628	AATTGTTTGTGAACC[A/G]CAAGGATTCTGGAGT	54476
rs541782898	snp	C/T	0.00358779	0.0422022	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5621132	CACCTGTCTTCAAAG[C/T]CTCCATCCTGGGCAA	54476
rs541789063	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5760197	TATTCCCTTTACAAA[C/T]CAATAAAATTCCCCA	54476
rs541789097	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5724394	CAACTATCTTGCAAA[A/G]TAGCACTTTCTCCAC	54476
rs541790917	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668380	AGGCACCCACCACCA[C/T]GCCCGGCTAATGTTT	54476
rs541798909	snp	C/T	0.0174175	0.0916809	intron-variant	RNF216	GRCh38.p7	7:5776556	GCTAAGATCGGGCCA[C/T]TGCACTCTAGCCTGG	54476
rs541799723	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750113	GCATATCTGTCCTTT[C/T]AATAAAAGGACACAA	54476
rs541802363	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5722475	GCTCACTGTCAGCTC[C/T]GCCCCCCGGGGTTCA	54476
rs541839730	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656972	AATCCAAAAGAAAAT[C/G]TGAGCCCACAGGCCA	54476
rs541852057	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652239	GAAATAACTCCATGA[A/G]GCTGCAGAGATGAGG	54476
rs541854488	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5646329	GCTGAGATCGCATCA[C/G/T]TGCCACTGCACTCCA	54476
rs541864030	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5755679	TATATGAATATAACA[C/T]AAAATTATTCCTTCT	54476
rs541891596	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5640641	CTTCTCACCATCTAC[A/G]GATACCATATAATGA	54476
rs541897149	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750537	TTCACTGAGTTTTTA[A/T]TATCTACCTGTTAGA	54476
rs541897683	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781614	TTACTCCTCAGAAGC[C/T]GCAGCTGCGAGCTCC	54476
rs541901357	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5742524	ACAGTATTTTTTTCC[A/C]TGTAAGACCGGCAAA	54476
rs541905906	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5778963	TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTTA	54476
rs541906110	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5659801	TGTGCCAACACCAAG[A/C]CTGGCAGGGGCAGGA	54476
rs541906208	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671697	GTAATCCCAGCTATT[C/T]GGAAGGCTGAGGCAG	54476
rs541918730	snp	C/G	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5751959	TTGGGAGGCTGAGGG[C/G]GGCGGATCACGAGGT	54476
rs541942640	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5773845	GTCCTGGGATAACAG[G/T]CGAGTCACCGTGCCT	54476
rs541959559	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681542	GCTAGGCAGGACCTG[C/T]AGCACCAAGGACAGT	54476
rs541971543	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5730260	TTGTGCTGATGGACA[C/G]ACAGAGGACATATGT	54476
rs541984930	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750874	TTTAACCCAGTCATG[C/G]GATGCGAGATTACCT	54476
rs541985023	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5745632	GGGCAGGGCACGGTG[G/T]CTCACGCCTGTAATC	54476
rs542036891	snp	G/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753892	CCCAGCTATTCAGGA[G/T]GCTGAGGCAGGAGAA	54476
rs542046525	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5729203	GTAGAAGGTATTACA[C/T]TCCATGTTTTTACGG	54476
rs542048928	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5728902	TCCTTCATGGAAGAC[A/G]CCTGTGTTACCCACC	54476
rs542053451	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5723515	AGCCGGACTCGGTGG[C/T]GGGCACCTGTAGTCC	54476
rs542073244	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5725492	GAAAATAAGAATACA[C/T]GAGACAGGCAATCCC	54476
rs542073393	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5759048	TTTCATAAATGATTT[A/C]GCACAATCCGTTCTG	54476
rs542084324	snp	A/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5651328	GCCTCCCTGGTTCAA[A/G]CAATTCTCTTGCCTT	54476
rs542089273	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5631438	TGAGGTGAGAGGCTG[C/T]AGTGCCTCCCTGGGT	54476
rs542137556	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216, RNF216-IT1	GRCh38.p7	7:5662176	AGAGGCAGGATGGGA[C/T]GGAATCAGACCTGAG	54476
rs542143850	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5726042	AGCACTGTGGGAGGA[C/T]GACGGGGGTGGATCA	54476
rs542156956	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5749437	ATTACAGGCGTGAGC[C/T]ACCACGTCGGGCCTA	54476
rs542171832	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5682956	TTTCCAACTCAGGAG[C/T]AAGCATAGGTAAACC	54476
rs542177113	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656564	CTCCCGCCCTCTCAG[G/T]GGGGAAGGAGCATGC	54476
rs542183093	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5731167	CAGCTACTCTTTGTC[A/G]AGAAAACTATGAACA	54476
rs542185120	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5726701	CGTCTCTAGTAAAAA[C/T]ACAAAAAATTAGCTG	54476
rs542202323	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5733786	AGAAATGTCACTTAT[A/G]CTACTTCATGCCTAC	54476
rs542235225	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5710223	AAATCAGTCAGGCGT[C/G]GTGGCGCATACCTGT	54476
rs542245623	snp	C/T	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5738496	GGTGGATCACGAGGT[C/T]AGGAGATCGAGACCA	54476
rs542257231	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5773308	AGTGCAGTGGTGCAA[C/T]CTCAGCTCACTGCAA	54476
rs542271785	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5739133	GTTCTGAAGATGGAT[G/T]GTGGTGATAGTTGCA	54476
rs542274376	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665871	GACATTTATATAAAA[A/T]TTCCAAGACCAAGGC	54476
rs542279878	snp	A/G	5.00856e-05	0.00500403	intron-variant	RNF216	GRCh38.p7	7:5641137	ATAAAGCAATAGGCA[A/G]CCATGTGTCTACTTA	54476
rs542289453	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5734196	ATTATTTGTGACAGT[C/G]AGAACTCAAATGCCT	54476
rs542310614	snp	G/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780342	CCCTCTACGTCACAG[G/T]GCTTCTTCTGTAGGT	54476
rs542311465	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5711274	GTAATATAGTCAGTT[C/T]TCATGAGGAGAAACA	54476
rs542313270	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5635534	CCTCCCTTTCACAGC[C/T]TTCCTCCCTAATTCC	54476
rs542352906	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5729900	TTCTATTACAGAATA[C/T]GTAAGAGAGACAGTC	54476
rs542355228	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666629	AGGGATCCCTTTCAC[A/G]GGGAGCTCTCAAGCC	54476
rs542359520	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5725083	CTCACACATGAATTT[C/T]CTAACACCACACAAA	54476
rs542396692	snp	A/C			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668650	AAAAGGGTCAACTCG[A/C]CACAGAAGAATGATA	54476
rs542414472	snp	A/C/G			intron-variant	RNF216	GRCh38.p7	7:5770998	TTGTTAGTAGAGACA[A/C/G]GGTTTCACCATGTTG	54476
rs542445213	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5688029	ACAATTTTCACTTTG[C/T]TTGATGGAAGGAACT	54476
rs542446738	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5639012	TAGACCATAGGGAGA[C/G]TCCTCAGTATAACAT	54476
rs542454179	snp	C/G	0	0	intron-variant	RNF216	GRCh38.p7	7:5650254	CATATATCACATTTG[C/G]ATGTTCTGCTCTTAT	54476
rs542466010	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5645832	TGACCTCAAGTGATC[C/T]GCCCACGTCAGCCTC	54476
rs542468791	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5693452	TTGTTCCCTGCTGAT[G/T]GGTATTGCATTGGAT	54476
rs542469340	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5758871	GACTGTTGGGAAGAC[A/G]CAATTGTATTTAGCA	54476
rs542487706	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5639430	TTTGAGAACCCAAAG[A/T]GCCGGGATTACACCC	54476
rs542507346	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5734880	TAAAAGGTTTGCAGG[A/G]CATGGTGGCTCACGT	54476
rs542524737	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5634260	CCTCCCCTTAGAAAG[C/G]TGACTGGGAATTGCA	54476
rs542526408	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5757047	ATTATCATGTAATTC[A/T]AAATATCTTCTAATT	54476
rs542530618	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5775625	CTGTAATCCCAAAAC[C/T]TTGAGAGGCCGAGGT	54476
rs542538125	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620550	CACGGCAGCCCTGTG[A/G]TCCCCCGTGCCTGGC	54476
rs542542335	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5777889	AAACATCAAGATTTT[C/T]TTCAACTGTCCAATG	54476
rs542563676	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5634233	GTGGCTTTTCTTCTT[C/T]ATTGCACTTTTCCTC	54476
rs542584668	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5704412	CAAGGATTAGCGACT[A/G]CTTTAGCCATCTTGC	54476
rs542597940	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670997	TCCGGGGGAGCTGCC[A/G]GAGTGGCAGCCTGCT	54476
rs542603661	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5743556	ATTAAGTGAAGAAAA[G/T]CAAGCTGCAAAATCA	54476
rs542610616	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768062	CAAGATGATTTGCCG[C/G]TACTCTAATTTGCAC	54476
rs542614022	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5623547	TCAACTGATCCACCT[G/T]CCTCACCCTCCCGAG	54476
rs542614657	snp	G/T	0.00597247	0.0543191	intron-variant	RNF216	GRCh38.p7	7:5772719	AGATATCAAAACCAG[G/T]TTAGCAAAGTTTTAC	54476
rs542623920	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5660017	TGGAGTGCAGTGGTG[C/T]CATTATAGCTCACTA	54476
rs542637593	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5691934	ACAGACCCCAGGGGC[C/T]GACAGTCAGGCCCTC	54476
rs542689338	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5624259	TGGCCAGTGGGGCCT[C/G]GGCTGCACACCGTTC	54476
rs542738266	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5758659	GTTTTGGACTTGTGT[A/G]GGACCTCTTGCGTCT	54476
rs542750944	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5758056	TACCTGAAAAAAGTT[A/C]TCATGATGGGTGCAG	54476
rs542759424	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5693116	CGCTATGGTATATGC[C/T]ACGGGTTGGCAAACT	54476
rs542777678	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5781861	AAAGGAAAGGAGACC[A/C]CCATATCCGACCCCA	54476
rs542783726	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5724406	AAAATAGCACTTTCT[C/T]CACCACTGAAGTCAG	54476
rs542800728	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5694312	CACTGAGCTTGCTTC[C/T]GCCACTGCTACTCAA	54476
rs542816266	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5635018	CTATGGGCACCTAAC[A/G]ACCATGTATTTGTGG	54476
rs542816878	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675300	AGAATTAGAAGCCCC[A/T]GAGGGGACAGGCTTT	54476
rs542819412	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5771972	GGCGTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	54476
rs542828744	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5778714	AAGTTTTGGGACTAG[A/G]TATTTTTCAGCACCT	54476
rs542864432	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5696630	CCTCTTCCTTGGCTG[C/T]TGCCATCCTCGCTTT	54476
rs542870906	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5709796	GTCTTAGTCTGTTGT[C/T]CAGGCTAGAGTGCAG	54476
rs542875755	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5655369	TTGGGAGGCCGAGGC[A/G]GAGGGATCACCTGAG	54476
rs542920970	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675839	CTCAGCCTCCTGAGT[A/T]GCTGGGATTACAGGC	54476
rs542927778	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5697230	CTGGTCAGGCCCAGA[C/T]CCATGTCGCTCATGC	54476
rs542941783	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667966	GGTTCCAGGGTACAG[C/T]GCAGCTTCAAGCTGA	54476
rs542945117	snp	C/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5762009	ACCTCTGTGTGTTCT[C/G]CAAGAAATACGCATA	54476
rs542978987	snp	C/T	0.00358779	0.0422022	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679897	CCCTGGGCAGGTGAG[C/T]CAGGCGGCTCCACAG	54476
rs542981780	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664514	TTCAAGACATGGAAG[C/T]TGATCTCTCTTCAAT	54476
rs542984333	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670650	TTCATTAGTTTCTTC[A/G]TGTCCGACAACCTAA	54476
rs542990240	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5728259	CCTCCCGTTTTACCC[C/T]TTCAAAGCCCCTCTA	54476
rs543045769	snp	G/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673532	TGACCTGTCACGTGG[G/T]GCAGTATGCAGGGAA	54476
rs543067153	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5649937	CAGCCAGTGAGGACC[C/T]TGATTATGTCGTTCA	54476
rs543073986	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5746838	GAATGTTCCAGATGA[A/G]AAAGAGTGTTCATCC	54476
rs543080780	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652037	GGCGTATCATTTTGT[A/T]TTCTGGAGGTGGGCA	54476
rs543089177	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5680366	TACCCGAGTCCTCCA[C/T]GTGGTGGGCTTGTCA	54476
rs543096624	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5775867	GAGCGAGATTCCATC[C/T]CAAAAAAAAAAAGAA	54476
rs543098712	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5752768	GGTGCTGTTCTACAA[C/G]AAGGCCCACAAGAGT	54476
rs543109009	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5692583	AGCCCGTGCAGAAGG[C/T]GAGCGAGGAGAAAGG	54476
rs543132870	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5718382	CGAGACTCCGTCTCA[A/T]AAAACAAACAAACAA	54476
rs543164015	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5632866	CAATGAGTACCATGA[C/T]GAAGCACACGAATGG	54476
rs543182943	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5708566	CTCAATAAATTACAT[C/G]AGATACTCATACTTT	54476
rs543183762	snp	G/T	0.00636936	0.0560724	intron-variant	RNF216	GRCh38.p7	7:5748072	TCCATACCAATAGGC[G/T]GTATCAGGCAAATAT	54476
rs543194631	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669045	CTAATATTATAAAGA[C/G]CATTAGAGAGTATTT	54476
rs543215944	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5657883	CAGTGAACTTTCTTT[C/T]CTTTTACTAAGGGAA	54476
rs543221962	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5756019	CCAAAAATCTCATCT[G/T]GAATTGTAATCCCAT	54476
rs543223776	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663923	AACAAAACAAAAAAA[A/C]CCCAAAACAAAAAAA	54476
rs543228661	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736971	CTGCCCGGCTGCCCC[C/T]TCTGGGAAGTGAGGA	54476
rs543270024	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5722747	GTTTTTGGGGCCAGG[A/C]GCAGTGACTCACGCC	54476
rs543316682	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5737251	TCTCTGAAACATGTG[C/G]TGTGTCCACTCAGGG	54476
rs543327397	snp	C/T			intron-variant, downstream-variant-500B	RNF216, RNF216-IT1	GRCh38.p7	7:5662151	CTGGAGAGCTGCGAA[C/T]GGCTCAGTAAGAGGC	54476
rs543381625	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675139	TTTAAATAATGGCAG[C/G]GAACAATGTAGTGAT	54476
rs543404316	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5648857	TGCAATGAATCTCAT[G/T]TGGATCCTAACCTGA	54476
rs543407301	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667859	GACTTAAAGTCACTG[C/G]ATCAGATTGGGGAAA	54476
rs543429819	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216, RNF216-IT1	GRCh38.p7	7:5662306	AGTTGCATGTCTGGC[A/G]GTATAGCAAAAGGAA	54476
rs543434666	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5718081	TAACAATAATGGTTA[C/T]ATATAAACAAAGCAG	54476
rs543442823	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682189	AAAGTTGGCAGATTC[C/T]GTACCTACGTGCCAG	54476
rs543451588	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781094	GATGTGAGGGAAGAG[A/G]AGGAAAAACGCCGCC	54476
rs543467619	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5747358	CAGGGGAAGGAGAGG[C/G]AGTAAAAACGGATAA	54476
rs543483067	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5736269	ATTGCAGGTGCGCGC[C/T]GCCACGCCTGACTGG	54476
rs543501583	snp	A/G			synonymous-codon	RNF216	GRCh38.p7	7:5623154	AGGCTTCTCCAGCGG[A/G]GGTCCAATGCGTTTG	54476
rs543517912	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5637865	ATTTCTTTTTCTTTA[A/C]GATCAAGTCTTGTTC	54476
rs543535544	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5626637	GCTACTGCACTCCAC[C/T]CTCCACCCTGGGCGA	54476
rs543553304	snp	A/G	0.000399281	0.0141238	missense, intron-variant	RNF216	GRCh38.p7	7:5741682	GGGTTGTTACACACT[A/G]AAAAATAGCTGCTCT	54476
rs543555001	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5644315	TGTATACTGGTGTCA[-/T]TTTTTTCTATATCTC	54476
rs543583999	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5758657	GGGTTTTGGACTTGT[A/G]TGGGACCTCTTGCGT	54476
rs543601677	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5721969	GCTCTGCTGCTCACG[C/T]TGGAGTGCAGTGGCA	54476
rs543612225	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5716946	GAGCTAGAAAATACA[A/G]GACAATATTTCTTAA	54476
rs543616681	snp	G/T	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664695	GCCGCCCAAGGGTAG[G/T]CTGCACGCTTCCCCC	54476
rs543623277	snp	C/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768925	CTCGACCTCCCAAAG[C/T]GCTGGGATTACAGGC	54476
rs543653562	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5646964	TTTTCTGAGCATGTG[C/T]TGAGCCCTAGACATG	54476
rs543682847	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5642097	AGATGAGGTTTAGAT[A/G]AAGTGCATTTAGTAC	54476
rs543689800	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5690789	GAGCTCATGCCCCGA[C/G]AGCCTGCAGGGATGT	54476
rs543701324	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5685664	AGAAGCCAACCTGAC[A/T]TCAGTCCTGGTCTCA	54476
rs543703140	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5779513	TTGAGATGTTTCATA[G/T]AATCTTCCCGCTTCT	54476
rs543718518	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622379	CCTCACAGCTGTGGC[A/G]GTGCCTCTGCGGGCC	54476
rs543749893	snp	C/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5660663	GCTCACTGCAGTCGC[C/G]ACCTCCCTGGCTCAA	54476
rs543789466	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672760	CTTCCTGGTGAGCAG[C/T]GCAAGGTAGAGGATG	54476
rs543794866	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5775080	GTATTTCCAATGCCT[A/G]GCACAGTTGTTGAAC	54476
rs543804669	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5765083	TAAAAAAAAAAAAAA[A/G]AGTAAGGATGGGATA	54476
rs543830988	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754643	AAATGGCCATAGTGA[A/G]TAAGACCCCTGCACC	54476
rs543833721	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5764286	CAGGCTATTGGACAG[C/T]AGTAAAAATAAAACC	54476
rs543845859	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620644	AGCCCAGTGTGGCCA[A/G]AACAGCTGGAACTCC	54476
rs543851092	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5700061	CACTCCTCTTTGCTA[C/T]TGTTCCCCTTCTCCA	54476
rs543864713	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5632430	GCTCCTTTCTGATGA[C/G]CAAGGCCAGGCTGAG	54476
rs543875747	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5700828	GCCATGGGTGGGCAG[C/G]ATGACCAGTGCCCTC	54476
rs543880461	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5647412	AATCATGGCTTACTG[C/T]GGCCTCGAACTCCTG	54476
rs543881630	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5770779	AGAAAAACAGACCAA[C/T]GGAACAGAGTGCAGA	54476
rs543884539	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5621080	GCTGCCCCCAAGCCC[A/G]GCCTCCCTGCGCACC	54476
rs543895999	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5632891	GAATGGCACCACAGT[A/G]GGCAGTGCACCCCAA	54476
rs543910032	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5751291	GTGGCACTGATGCCC[A/G]AAGGTTTGGTCAGGT	54476
rs543931642	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5721731	TTTTAGCCATTCTGG[C/T]GGGTGCAAATGTGCT	54476
rs543961258	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5684415	CCTGGCCCACAAGCT[C/G]GGCCTTCTAAGCCGA	54476
rs543962011	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5689121	ACCATCAGTGCCTTG[A/T]GAGCCAATATGCAGA	54476
rs543989057	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5705254	CTGGATGTCTCCCCT[A/G]AAAACTCAACATGTC	54476
rs543995446	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678006	ACCAGATTTTGCGAC[G/T]GTTCTTGGTATTCTA	54476
rs544011159	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5749149	CAAAAATGCCCATGT[-/A]TTTTTTTTTTTTTTT	54476
rs544014123	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5699436	AAGAGTTTTATTAGC[A/G]AATACCTAGACCTCA	54476
rs544016871	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5627146	CCAACCTCTGTAGCA[C/T]AGAAACTGAGGTCCC	54476
rs544019653	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5745078	GTACACACAAACCTA[C/T]GGGCCAATCTCCACC	54476
rs544031502	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5647258	TGTATTTTTTGAGAA[C/G]AACTAAAGTTTGGTG	54476
rs544032464	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671662	ACAAAAAAATCAGCT[A/G]GGCGCGGTGGCGGGC	54476
rs544049326	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5705671	CCCAGCACTTTGGGA[G/T]GCCAAGGCAGGCAGA	54476
rs544054433	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750481	AAAATTACATTTCAA[A/G]AGAAAACTCCAGTAT	54476
rs544062986	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5710632	CAGTGTGCTGCATGG[C/G]CCTGCCCCTACTCAG	54476
rs544063753	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5699405	GATAAGGAGTAAAAA[C/G]CCCCTAAAACCCAGG	54476
rs544074024	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5722064	GGAGCTGGGACTATA[C/G]AGGCAGATGCCACCA	54476
rs544075797	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5696259	TCAGCAGCTGGGAAA[A/G]CATGTTGCAAAAGGA	54476
rs544076630	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5779952	TGCTCTGGTCCCCCA[C/T]CTACATCCCATTCAG	54476
rs544103724	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5635467	AAATCAGTTTCCAAC[C/T]TAAAAGTCTAAAATA	54476
rs544105452	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5625311	CCTGATATCGTGAGA[C/G]GATTAGCAAGTCCCA	54476
rs544148480	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5725575	GGTAGTGGCAGCTGG[A/G]TGCGGTGGCTGACGC	54476
rs544170066	in-del	-/TT	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753036	TATCACATCCAACTC[-/TT]TAAGTTTTTCCTGAC	54476
rs544191695	snp	A/G	0.000159962	0.00894177	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739596	ACAGATCCATTCTTC[A/G]TTGCTTCAACAAATA	54476
rs544198698	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5759147	TTGTTCCTGCTCCAG[C/G]CATGTGAGACAAGCG	54476
rs544216701	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5661554	ACTCTTGTAATCCAA[A/G]CATTTTGGGAGGCCG	54476
rs544223327	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754237	CATAGCTCACTGCAG[A/C]TTCAACCTCCTAGGC	54476
rs544229196	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5778013	CTTCTGTGACCAAAG[A/G]ACATGCTTCTGCTTC	54476
rs544243395	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5779047	CACCATTCCCAACTA[A/T]GTTCTATTATCTTTA	54476
rs544253523	in-del	-/TCT			intron-variant	RNF216	GRCh38.p7	7:5760598	AAGGCTAAGCCAGAA[-/TCT]TCTGGCAAAAAAGAA	54476
rs544278908	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5682753	TAGAGTTAGAATAAT[C/T]ATGTGCAACACTTTT	54476
rs544280781	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676486	GGAACCCCACCGAGC[C/T]GCACCTGCATTGAGT	54476
rs544290016	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5760138	AATTCGAATTTAACA[C/G]GAAATTTCACAAACA	54476
rs544296457	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5689542	TAGGCTTGTAGTCAA[A/G]TAGTTTTCCTTTTCT	54476
rs544309854	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5783477	GCTGTGAGCTATGAT[C/T]GCACTGCTGCACTCC	54476
rs544317690	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5772871	CAACCCTCTGCATCC[C/T]GGGTTCAAGCAATTC	54476
rs544326132	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5726367	TCTGTAGGCAAATCT[A/T]CCATGTTGTTTCTCT	54476
rs544330453	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750241	GTAAATCTGTCTCTT[C/G]CTGGCAGGCTCAGGA	54476
rs544344685	in-del	-/A	0.0023933	0.0345097	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674834	AACCCCATCTCTACT[-/A]AAAAATACAAAAATT	54476
rs544365569	in-del	-/A			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679134	AACATCTTAGTTATC[-/A]AAGTCATTTAATCCT	54476
rs544384723	snp	A/G	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5634992	TACCTGGTTCATGGG[A/G]CTCAGGGACCCTATG	54476
rs544403116	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5660441	GGAATACAGGCGCCC[A/G]CGACCACACCTGGCT	54476
rs544404438	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5739117	TTGAGAAGATGAAAG[A/G]GTTCTGAAGATGGAT	54476
rs544408589	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5640457	CCCCTGGGCCAATCG[C/T]TGTCACCTCCCTGTG	54476
rs544409242	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5758123	GTCAGTAATTTTCCA[A/G]AATGAATTAGTTGTT	54476
rs544454321	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5706162	AAGGTGGAGGTTGCA[A/G]TGAGCTGAGATTGCA	54476
rs544457101	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5766358	ATGCTCTAAAGTGTG[C/T]CACGCCTGGCCTCCA	54476
rs544476643	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5763913	AAAACAGACGGCAGG[A/G]CACGACAGCTCATGG	54476
rs544489317	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5735036	CTGTAATCCAAGCTA[C/G]TCAGGAGGCTGAGGC	54476
rs544496969	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5631266	ATGTGCCATCCCCTG[A/T]AACAGCCCACTTGTC	54476
rs544498064	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753187	GGGAACTGCTAGAGA[A/G]CATCTAACAATTACT	54476
rs544506079	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681887	TTCAACATGAAGACG[A/G]GATCTGTGTAGCCCC	54476
rs544521471	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666974	CACATGCCACCATAC[C/T]TGGCTAATTTTTTGT	54476
rs544525926	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5735397	GAACTTAACATATCA[C/G]AACAATCAAACTCAC	54476
rs544536049	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5730402	GTTAAGAGTTTTGGC[C/T]AATTCTTGTTTTGCT	54476
rs544541074	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753851	AATACAAAAATTAGC[C/T]ATGCGTGGTGGCGCA	54476
rs544576065	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5693059	AATATCTTGGAGACA[C/G]CTCCATATTTGCACA	54476
rs544582336	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5687878	TCTCACCATTTTACA[A/G]ATGAGGAAACCAAGT	54476
rs544586055	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5737463	ACCTTCCCTCCACTA[A/T]TGTCCTGTGACCCTG	54476
rs544603347	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5715337	AAACAATGATATGCT[C/G]TTTCGTGCTATATAA	54476
rs544613875	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5720734	ATTCCAGCTGACTTG[C/T]ACATTTGATACTATA	54476
rs544630769	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5639393	CACATAGAGGAGAAA[C/T]ACACTTCTGTTTTCC	54476
rs544650519	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5743717	GATACATGCTAAACT[A/G]GTAACAACAGTTCCT	54476
rs544667323	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5646241	GGGCATGGTGGTGCA[C/T]GCTTGTAGTCCCAGC	54476
rs544668861	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5655563	GTGAGCAGAGATCGC[A/G]CCACTGCACTCCAGC	54476
rs544669168	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5640047	TACAGGCGTGAGCCA[C/T]CGCGCCCGGCCAATT	54476
rs544673679	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5737945	ATACAAAAATTAGCC[A/G]GACAGGGTGGAGTAC	54476
rs544694838	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670571	AATGTTTATGAGCAA[C/G]AAATTAATGGTATGC	54476
rs544698222	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663967	TGCCTATTCTGTGCC[A/G]CATGGAGATGCGATG	54476
rs544727393	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5709700	CACCAACATGCCAAG[C/T]TGATACTCACTAGAT	54476
rs544731269	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665202	AGGGGATTCCTCTCT[A/G]TCCTCAAAGTACAGT	54476
rs544735972	snp	A/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671386	CTCCCTCAAATGCAT[A/T]TGTGAAGCCCTCAAC	54476
rs544762172	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5738637	GGCCTGAACCTGGGA[A/G]GCGGAGCTTGCAGTG	54476
rs544816771	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643817	AAGGAAACCCTGTAC[C/T]CACTAAGCAGGCATT	54476
rs544822267	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712452	TACTCCAGCCTGGGC[A/G]ACAGAGCGAGAATCC	54476
rs544822654	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5686830	GCATTAGACTCTCAT[A/G]AGGAGTGTGCAACTC	54476
rs544854890	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5698438	ACACGCATGCATGCT[A/G]GAGTACAGTGGCATG	54476
rs544859981	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5773960	TCATTTTTACAGCTA[A/G]TTTAGTTGAAATGTC	54476
rs544862690	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5624218	CTTGTTGCTTATGGC[C/T]ATGGAACAAGCCCGA	54476
rs544875589	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5654539	TAAAAATACAAAAAT[G/T]AGTTGGGCGTGGTAG	54476
rs544884031	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713766	GACGACATTTTAAAA[A/G]TAACTAGCTAAAATT	54476
rs544889446	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5649780	GACAGTGTATTACTT[C/T]AAGCCTCAACAGATG	54476
rs544893615	snp	A/C	0.00636936	0.0560724	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665271	AAATGCAGAAATTCA[A/C]ATCTGGGAGTGGCCA	54476
rs544900530	snp	C/T	0.000798403	0.0199641	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619877	GATCACCTGATCTTC[C/T]TCCCTGGCAGGGGAG	54476
rs544900898	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5624590	GACAAATGTCCAGTC[A/G]GGCCCTGCTTAGCCC	54476
rs544927689	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5638464	CGCACTACATCTTCG[A/G]ATCTGTACACAGTAA	54476
rs544930468	snp	A/C			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753257	GAAATCTGTTTACAA[A/C]ATTTTCTTGACTGCC	54476
rs544937732	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620169	AAGGTAAAGAAAAAG[G/T]TTAATGAACTAATCG	54476
rs544940707	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670047	TTCTCCTGTCTCAGC[C/T]TCCCGATTAGCTGGG	54476
rs544949077	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5742283	AACTCCTGGCCTCAA[A/G]TGATCCGCCTCCCTC	54476
rs544951581	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5720261	AGACAGCAAAACCAA[A/C]ACACCCCTCCTCCTC	54476
rs544953812	snp	C/T	0.0103295	0.0711199	intron-variant	RNF216	GRCh38.p7	7:5725035	TTGAGACCAGTTTTT[C/T]CCCCCAAGCTTAACA	54476
rs544974417	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5777383	TTTCTAGCCAATGGG[A/G]AGCAATGCAATGACA	54476
rs544997077	snp	A/C/G			intron-variant	RNF216	GRCh38.p7	7:5772639	TACAAAGAGTTAATA[A/C/G]TCAAATAATATCAGC	54476
rs544998079	in-del	-/AT	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5642568	GTTCAAACGGTTCAC[-/AT]GTCTCAGCTTCCCAA	54476
rs545014368	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5633807	CGGCCTTTCCAGAAA[C/T]GTGCTGCACTTGAAG	54476
rs545038797	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622650	CATCGCAGCTCTCTC[C/T]GAACTCCACCATTTG	54476
rs545039693	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5644667	ACACCACCATGCCCA[A/G]TTAATTTTTAAATTT	54476
rs545056380	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5628884	GTTTCTCTGAAGCAT[C/T]TGAAATTCCTCAAGT	54476
rs545064225	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5772440	AAATGTGCTTCTTGC[G/T]GTGTCACCCAGGCTG	54476
rs545073835	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5703571	AAAAACAGCAAATGC[C/T]ACAAAGAATAGGATG	54476
rs545075166	snp	A/G	1.64974e-05	0.00287201	missense	RNF216	GRCh38.p7	7:5623032	ACAGGCCGCACGGGA[A/G]GCAGGGGGAAGGGTG	54476
rs545081522	in-del	-/TTAAT			intron-variant	RNF216	GRCh38.p7	7:5645588	ATTTCTGTTGGTTTC[-/TTAAT]TTTTCTTTTTTTTTT	54476
rs545085503	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5697311	TGGTCAGTTAGGGCC[A/G]TGGTTGCCCTTTCTC	54476
rs545094439	snp	A/G	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5733695	GGAATTCAAAGAGAA[A/G]AGAGAAGTAAACAAT	54476
rs545100536	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5690903	TTCATCATGGAATTG[C/T]GATTTGGGGGCTGAA	54476
rs545141953	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5649985	TCTACTTGAACGACA[C/T]GCAGATAGAACCTGG	54476
rs545148825	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5697800	GTAGTAGGTGCTGGC[C/G]TTGAGGGTGAAAAGT	54476
rs545152464	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5775798	TGCTTGAACCCGGGA[C/T]GCAAAGCTTGCAGTG	54476
rs545164339	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5649376	ACAGACGGAGACTCC[A/G]TCTCCAAAGGAAAAA	54476
rs545182921	snp	A/G/T			intron-variant	RNF216	GRCh38.p7	7:5756841	GAATCTCACCATGTC[A/G/T]CCCAGGCTGGCCTCG	54476
rs545208732	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5752122	ACCAGAAGGCGGAGG[C/T]TGCAGTGAGCCAAGA	54476
rs545211619	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5752627	AGTGGAATTTGGTGC[A/G]TTAATAGTCAGATGG	54476
rs545246331	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5748005	TCAGGGTGACTGGTA[G/T]AGCAACTCCCTAAAT	54476
rs545246503	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5707800	ACAATCTCTGCTCAC[C/T]GCAACCTCCACCTCC	54476
rs545254802	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5702082	TCGCTGCCGGGTTCT[C/T]GGAGCCCACGCTGAC	54476
rs545260060	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5637494	AGAGAACACCTGGTT[A/G]CCACAGAGGACTCAC	54476
rs545302245	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681066	CCTTCCCACACTGGG[G/T]TCTCAGCTCCTGTGT	54476
rs545314789	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5702609	AACACATCTACTCTA[C/T]GCTGTATTTACTGTG	54476
rs545315208	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5625875	AATTCTCCTACATTC[C/T]CTAGGCCTCAGATGC	54476
rs545361823	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5685245	TAGCTGGAGACAGTG[A/G]GCACGAACAAAACCA	54476
rs545378944	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5732676	TGGAGGCACAGAAAA[G/T]GAAGGACAAAGTTTT	54476
rs545382596	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663823	GAATCACTTGAACCC[A/C]GAAGGCAGAGGGTGC	54476
rs545383076	in-del	-/AG			intron-variant	RNF216	GRCh38.p7	7:5747775	AAAAAAAAAAAAAAA[-/AG]GGGAAAAAAAAAGAA	54476
rs545383587	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5633202	CAGGCTGGTCTCGAA[C/G]TCCTGACCTTGTGAT	54476
rs545383651	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5732215	ATTCACTGGTGTGCA[A/C]TGAGGTTATGCAAAC	54476
rs545394318	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5761517	TTTCAGCCAGACGCA[A/G]TGGCTCACGCCTACA	54476
rs545419425	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5696544	AAGGAGGAGCAGGCC[A/G]GGGCAGCCTCCTAGA	54476
rs545425883	snp	C/G	0.00199481	0.0315187	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5780117	TAAAACAATGCCAAC[C/G]CAGCCCCTTCCAGGA	54476
rs545430474	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5761988	CCAGGTATATCAGCT[A/G]AAGAAACCTCTGTGT	54476
rs545430819	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5718252	CAGGCATGGTGGGGC[A/G]CACCTGTAATCCCAG	54476
rs545452537	in-del	-/G	0.00159617	0.0282053	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622344	GCACGGGTTTTGGAT[-/G]GGGGGGACAGCATCT	54476
rs545510884	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780597	AGCTGAGGCAATCCC[C/T]GTGAGGCTGAGGCAG	54476
rs545517748	snp	G/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5757058	ATTCAAAATATCTTC[G/T]AATTTTCATTGTGAT	54476
rs545520233	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5734701	AGGTAACACATGCCT[A/G]TAATCCCAGCTATTC	54476
rs545538276	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674308	GTTGGGATTACAAGC[A/G]TAAGCCACTGTGCCT	54476
rs545549743	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5640369	CCCCAGCGTAGTAGC[C/T]AGTGTGACCTGGGAA	54476
rs545553729	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216, RNF216-IT1	GRCh38.p7	7:5662216	TCTTACTGGTAACGA[C/T]AGGAACCTGCTAATC	54476
rs545555191	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712589	TTATTGATAATCTTA[C/T]TTCTCAGCAAGAAAT	54476
rs545571137	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713191	AGTTGTTCCCCTCTA[A/C]AGATATTAGAAAGCT	54476
rs545597973	snp	A/G			intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5651956	CTGGCCTGCATTTTA[A/G]TAAGTGAGTATTTGT	54476
rs545607459	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643169	AACAGCTATTCAATA[C/T]TGCTGAAATGTTAAA	54476
rs545609906	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5637847	CACCAGGCCAAATTA[C/T]GCATTTCTTTTTCTT	54476
rs545669041	snp	A/C			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673509	GGTGATGTGAAGAAC[A/C]GCAAAGCTGACCTGT	54476
rs545692521	snp	A/T	0.00557542	0.0525036	intron-variant	RNF216	GRCh38.p7	7:5760805	TTATTAATCCATTTG[A/T]AATGAATGAGTCTTA	54476
rs545698668	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5684590	TCTGGCTGATGTCAG[A/G]GGCAGTAAAGCCCAT	54476
rs545720065	snp	A/G	0.0166325	0.0896639	intron-variant	RNF216	GRCh38.p7	7:5736889	CTCCGCCCGGCAGCC[A/G]CCCCGTCCGGGAAGT	54476
rs545764664	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5692377	TAAAAAGCGGTCATA[A/G]CAACGCCGGGTGAAT	54476
rs545770577	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5745551	GAAATTAAGAGTCAA[A/C]TGAAAAATCACTACA	54476
rs545814803	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652285	GGTTAGATTACTTCC[A/C]CAAGATCACTCCAGA	54476
rs545823487	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5726503	CTTCCACTGGTGAGG[A/T]TCCCTTTTCTTTCCT	54476
rs545829471	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5648126	TTTTTTTTTTCTTGA[A/G]ATGGAGTTTTGCTCT	54476
rs545849667	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672300	AAATACATGTTTACT[C/T]TGGGGGAATGATAAT	54476
rs545853187	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5718017	GGGTAAATAAAAATA[C/T]GTATACTTATTTGCT	54476
rs545861055	snp	C/T	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5739996	TGACAGAGTGAGACT[C/T]GGTCTCAAAAAAAAA	54476
rs545871185	in-del	-/C	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5690512	TCTCCTCTCCCTGCA[-/C]CATCTACCACTTAGA	54476
rs545878071	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5751038	GTTGGGGCCCTAGCC[A/G]AGGAGCAGCCTCCAC	54476
rs545906927	snp	C/T	0.0123036	0.0774623	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621391	CCCGACCTCAACTCA[C/T]CCGCCCGCCTCGGCC	54476
rs545907121	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5636334	CCTTCTTTATAAGAC[C/T]CTTAGTTGAATGCTT	54476
rs545927896	in-del	-/A	0.373397	0.217424	intron-variant	RNF216	GRCh38.p7	7:5779657	TAGACTCCGTCTCTT[-/A]AAAAAAAAAAAAAAA	54476
rs545933546	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768645	AGGTAATTCTGAAAT[A/G]TGAGAAATGAAGCAA	54476
rs545946381	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5746104	AAAAACGGCTAACTC[C/T]CTTTTTTGGGAAGTA	54476
rs545964807	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5740658	TAATTCAATAAAACT[A/G]CTTTAAGGGTTTCCA	54476
rs545984133	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5651384	GGTGCGTGCCCACCA[A/C]TCCTGGATAATTTTA	54476
rs545986704	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5735807	AATTGATAAAGATTA[A/G]GGGAAGGCCAGGTGC	54476
rs546001627	snp	A/G			utr-variant-5-prime, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781723	ACAGGAAGAACCATA[A/G]AGGCACTCCGGGTAC	54476
rs546004272	snp	A/G	0.0166325	0.0896639	intron-variant	RNF216	GRCh38.p7	7:5646408	CAAAAGGAAAAAAAA[A/G]GGGGGCCAGGTGCCG	54476
rs546031648	snp	A/T	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5756072	GACAGGTGGAGGTAA[A/T]CGGATCATGGGGGCA	54476
rs546041376	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5646836	TCCTGATCTTTGCAG[C/T]TGGAGTACTCTGAGT	54476
rs546042220	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5726499	AATCCTTCCACTGGT[A/G]AGGATCCCTTTTCTT	54476
rs546058727	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5626528	TTGAGACCAGCCTGG[C/G]CAACAAAGTGAGATC	54476
rs546061615	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5709392	CCAGCCTTTGATGCA[A/G]CTGGTTTCTGGATTT	54476
rs546075742	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5755370	TACTTAAAAAAAAAT[G/T]GAAAGAATAACACAG	54476
rs546083705	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5690100	CTGGGAGGCTTAGGC[A/G]GGCGGATCACCTGAG	54476
rs546093849	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621950	CACCCGGGGCACACA[C/T]GGGGCAGGGGTGGCA	54476
rs546122568	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5691265	CCACTCGGGCCGACG[A/G]CAGCATTTGACTGCT	54476
rs546124950	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5729309	ATCTATTTATCTTCA[C/T]CCTAATAAATTCCTT	54476
rs546129380	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5744981	CCATCTCCAAAAAGA[A/C]AAAAAAAAAAGAAAA	54476
rs546134293	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750168	GCTTTGACTGGAATG[C/T]CATATTTCAAAATGT	54476
rs546149793	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5722172	TAAATGATCCACCAG[C/T]CTTGGCCTCCCAAAG	54476
rs546172149	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5779490	TTCCTTAAAGCAAGC[C/T]GACTAAATTGAGATG	54476
rs546182898	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5735088	AAGACGGAGGTTGCA[A/G]TGAGCCAGGATCACG	54476
rs546238166	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5655368	TTTGGGAGGCCGAGG[A/C]GGAGGGATCACCTGA	54476
rs546246624	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5735462	AAAAGATTAAAAATA[C/T]AGGCAAAGAGCAAAA	54476
rs546259814	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5774577	GTTACCTGCGAAACA[A/G]AAAAATCAAAATAGC	54476
rs546262831	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672846	GGGGCTTTCTAGGAC[A/G]CAGGGACACAGGCAG	54476
rs546263992	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5706279	AAACTACCCAATTAA[C/T]ACATTTTTAAGTGTA	54476
rs546272951	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5715439	TATTCTTTAGAGTAA[G/T]TCTTTATATAAAGTT	54476
rs546276410	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5706693	ACAGGAACATGCTGA[A/G]ATCCTTTCCCAAAGG	54476
rs546286779	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5631498	GCTGTTCTCAGCTCA[A/C]TGGTTTTGGTCCATC	54476
rs546298024	snp	C/G			intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5766895	GAGACTGATATTCAC[C/G]AGATAGCTGTATAAT	54476
rs546313218	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5623838	CTTGGGACTTCCTCA[A/C]CATCAAGGAGATGCC	54476
rs546314436	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5755827	AAATGCTGAGTCATG[G/T]GGTAAGCATATGCTC	54476
rs546315905	snp	C/G	0.00119737	0.0244387	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619946	CTGCCAGGACCCAGT[C/G]GGGGAGGTGAGGATG	54476
rs546325255	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5631887	CACGCTCTGCCCCCA[A/C/T]GAGGTCCTGCTGCCT	54476
rs546328904	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5645276	ATAGACTCTTGTTCT[C/T]CATCAGATTTGGGAA	54476
rs546348805	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5700481	CACAGAAAAATGTCA[C/T]TAAATTATTTTAGTA	54476
rs546371737	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5703857	ACTTGACTTACACAG[C/G]TCTGAGTTTATAAAG	54476
rs546373361	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5721431	TCCTGTCACTAGTGT[A/G]CTATGTGAATATACC	54476
rs546382103	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5633864	AGAGGTTTTAATTAA[A/G]AAGAGAGAAACAAAA	54476
rs546386760	snp	A/C	0.0103295	0.0711199	intron-variant	RNF216	GRCh38.p7	7:5683074	TTAAAAAACAAAAAA[A/C]AAAACCGCAGGGCAC	54476
rs546389850	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5715932	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCACGTT	54476
rs546389979	snp	A/G	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5772092	TACAAAATTAGCTGG[A/G]CATGGTGGCCCATGC	54476
rs546393845	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5749545	ATAATTTTGGTTCAG[A/G]AATAACTAAATTTCC	54476
rs546407330	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5783629	GGCTTATGGGGGCTT[C/G]CATGGGACAGAAAAA	54476
rs546415002	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5629248	TTGGGAGGCTGAGGC[A/G]GCAGGATCGCTTGAG	54476
rs546429941	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5772516	GGTTTAAGCGATTCA[A/G]TCCTTTCCTTCCTCT	54476
rs546430877	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5640808	CTGTAGTTTTCTTTG[G/T]TAGGGCTATCTCCGT	54476
rs546437086	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5704477	GAGAAAGGTAAAAGC[G/T]TATGCGCTAATAACA	54476
rs546453674	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5629750	GAGAATCACTTGAAT[C/G]TGGGAGGCAGAGGCT	54476
rs546471754	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677439	GGCTTTCCTCTATAA[A/G]AGGAAAACAAAAAGG	54476
rs546502554	snp	A/C/T	0.00159617	0.0282053	upstream-variant-2KB	RNF216	GRCh38.p7	7:5783290	ATGTGCCACCACGCC[A/C/T]GGCTAATTTTCGTAT	54476
rs546513647	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5683737	ATTACAACTGTTTTT[A/G]AAGTGCTCAGCACAG	54476
rs546526345	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768155	AATGTCCAGACTTTG[A/C]TTAAAAAAAAAATTA	54476
rs546531281	in-del	-/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669931	TGCGTTTGGAAATCC[-/T]TTTTTTTTTTTTTGA	54476
rs546534547	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5698053	CATACAAGCTTCTGA[C/T]GGGAAATAAAACTGA	54476
rs546535548	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5729672	ATCATTTTAAGAATT[A/G]CATGTGTAGAAAAGA	54476
rs546544751	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5733873	GCAATTCACACATAT[A/G]AGTTGCTTTTTAGAT	54476
rs546575743	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5648564	CCCCGTCTCTACTAA[A/T]AATACAAAAAAAAAT	54476
rs546591207	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5758299	GGCTACAATCACTAC[C/G]AAGTTAGAATACATT	54476
rs546594241	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5720450	ACCAAACGTGCTCAT[C/T]GACTATTATGGGTAA	54476
rs546596546	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5708945	CCGTGGGTCCTCTGG[C/T]GCAGTACAAACCACC	54476
rs546629762	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5758695	TTGGCCAATTTCTCC[C/T]TTTTGGAACAGGAGT	54476
rs546645635	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5633594	AAAACAAAACAAAAC[A/G]AAACAAAAACAAGGA	54476
rs546648443	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5687463	GGGGACATGATGTGG[C/G]ATTTTCAGAAACCAA	54476
rs546669934	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5748743	TTAAGTAGTACTAAG[C/T]AGTTAAGGCTTTGGT	54476
rs546677537	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5719782	ATACCTATTTTGAAT[A/G]ATCATAGTTTTTCTG	54476
rs546687208	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782689	ACCCCGTCTCTACTA[A/G]AAATACAAAAATTAG	54476
rs546706803	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5714957	GCAGAACTCCACCTC[A/G]CCCTCAAAGAGGCAC	54476
rs546711731	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682133	GCGGGCCCACGCTGC[C/T]AGGAAAAACCGTTGG	54476
rs546719111	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5626699	AGGAAGAAAGAAAAA[A/G]GAAAGAAAGTTGTGC	54476
rs546722164	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB	RNF216	GRCh38.p7	7:5783279	GGATTACAAGCATGT[C/G]CCACCACGCCCGGCT	54476
rs546733308	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5639122	AAGTTCTGGCTGATG[A/G]GACTGAAGCAGAAGT	54476
rs546775524	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675486	ACGAAAAATAAATTT[A/T]AAAAAATTAGCTGAG	54476
rs546805097	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5770221	AACCCCAGCACTTTC[A/G]GAGGCCAAGGTGGGC	54476
rs546819990	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5697471	GTTTAGAGGAGAAGA[C/T]GAAGTGTCAGGCAAG	54476
rs546820849	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5686096	GGCGTGGTGATGCAC[A/G]TCTGTAATCCCAGCT	54476
rs546836320	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5623816	ATTCCTGAGCTCAAA[C/G]CCACCCCTTGGGACT	54476
rs546836868	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5658811	TGTAACGTACAAATA[A/C]ACACATACGCTGGGG	54476
rs546844535	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5691061	GCTCACACAGCCGTG[C/G]AAAGAACTCTGTTCT	54476
rs546851356	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5756837	ATGAGAATCTCACCA[A/T]GTCGCCCAGGCTGGC	54476
rs546859413	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5696818	GACGGCATGTCCCCA[C/G]GTTACTAGAAATGAC	54476
rs546875411	snp	A/C	0.000399281	0.0141238	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619650	GCCATGGCCTCTCAG[A/C]CCAGGCACTTCCTGT	54476
rs546890586	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781552	TCACTCGTCACTCAA[C/G]TCGCCGGCTAGCCAG	54476
rs546903316	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665452	CTTTGAAAAAAGAAA[A/T]CTTGAAGTGTTATTT	54476
rs546905185	snp	A/G			utr-variant-3-prime	RNF216	GRCh38.p7	7:5621322	TGGGATTATAGGCAT[A/G]CGCCACCTTGTCCGG	54476
rs546952732	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643948	GGAATGGAAATCACA[C/T]GTGTGTTTTTGTGCC	54476
rs546955053	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5759722	CTACAACCTCTGCCT[C/T]CCAGGTTCAAGTGAT	54476
rs546963948	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669071	TATTTCAACGCAGGC[A/T]GGTGGCTACAGATGG	54476
rs547004693	snp	A/G	0.000498081	0.0157731	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752858	CACTTCTGTCAGGAT[A/G]ACATCATCATCCAGG	54476
rs547005628	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675051	ATGTCGGTACAGAAT[G/T]GCAACTGCTGAAAAG	54476
rs547032528	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5644386	TCCTAATAGGTGTGA[A/G]GCGGTATCTTATTAT	54476
rs547049219	snp	C/T	0.0174175	0.0916809	intron-variant	RNF216	GRCh38.p7	7:5735545	CAGTAACACGGTAGA[C/T]GAGTTAAAAGGAGAT	54476
rs547059645	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5701575	GTGCAACCGTTCTTA[C/T]TGTACACGGAAAGGA	54476
rs547069713	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5637908	TGGAGTGCGGTGGCG[C/T]GATCTTGGCTCACTG	54476
rs547075785	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5761678	GTAATCCCAGCTACT[C/G]TGGACACTGAGGCAG	54476
rs547095484	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5652593	AAAAGGGATATGAAA[A/T]GAGCTTTACTTGGCT	54476
rs547108266	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5691058	CCAGCTCACACAGCC[A/G/T]TGCAAAGAACTCTGT	54476
rs547115333	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5737660	AGAAAAAAGTACCTA[C/T]ATTGGGCTAAGCACC	54476
rs547124087	snp	A/C	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670213	TGCTGGAATTACAGG[A/C]GTGAGCTACCGTGCC	54476
rs547127148	snp	G/T			upstream-variant-2KB	RNF216	GRCh38.p7	7:5782810	CAGTGATTATGCCAC[G/T]GCACTTCAGCCTGGG	54476
rs547156924	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5650619	TTCCCAACTTCTACA[A/G]GCTACCTCAATCCTT	54476
rs547174474	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5757273	TGCTTTGTATATTTT[C/T]CTATCATGTTACTAA	54476
rs547175179	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5653911	CTGGACTGCAGACAG[C/T]AAGCATGGCCCTGGA	54476
rs547178460	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5732778	GTCGGACTTCAATCT[C/G]CCCACCTCTTCATAT	54476
rs547206589	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5746607	TGCAAAGTGATTGGC[C/T]AGGTAGGACATCTTG	54476
rs547236545	snp	A/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5654249	TAGAGATGAGTCGCC[A/G]TGCCTGGCCCTTTTG	54476
rs547251855	in-del	-/A	0.0023933	0.0345097	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663468	TTCGCCTGTAGTCCC[-/A]AGCTACTCGGGAGGC	54476
rs547254318	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5642341	ACTTCAGTCTCCCAA[A/G]TAGCTGGGATTACAG	54476
rs547263871	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5752345	AAGTAGCCTTGACTA[C/T]ATGAAAAGACAAAAT	54476
rs547277242	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5740022	AAAAAACAAACCAAA[A/G]ACAAAACAAAAAAAA	54476
rs547292340	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680707	GCGCCCAGCACTCAA[C/T]ACTTCTACTTGGATA	54476
rs547300579	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5775595	GCAAAGCAGGCCAGG[A/T]GCAGTGGCTCACACC	54476
rs547308009	snp	A/C	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5719217	GAAACCCAGGCTCTA[A/C]AAAAAAAGTTAGCCA	54476
rs547328495	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5740855	ACATCTAGATATATA[C/T]TTCTTAGGAAAATGA	54476
rs547346463	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5726675	CCAGCCTGGACAACA[A/T]GGCAAAACCCCGTCT	54476
rs547358106	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5649503	GACAGAATAAGACAC[C/T]GTCTCAAGGCGAGAA	54476
rs547360125	in-del	-/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5626751	ACCTCTTAGCTAAGT[-/G]GAGCTCGGCAGGTTC	54476
rs547388863	snp	A/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5770974	CACCACGCCCGGCTA[A/T]TTTTTGTATTGTTAG	54476
rs547402355	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5756369	CTTTCATGCTACAAT[A/G]GTATAGCTGAATAGT	54476
rs547408574	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5632637	CAAAAATTAGCCAGG[C/T]GTGGTGGTGGGTGCC	54476
rs547409814	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5727111	GTCCCAGTCTGGGCA[A/G]CAATGAGAAGCGGGG	54476
rs547417182	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736465	GGCGCGATCTCGGCT[C/T]GCTACAACCTCCACC	54476
rs547423174	in-del	-/CAAAA	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5646373	GGCGAGACTCCATCC[-/CAAAA]CAAAACAAAACAAAA	54476
rs547426416	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5696078	ATCCCTGACTCCCAG[A/G]AGGCACGGAAGGACA	54476
rs547441268	snp	A/C/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754598	GGTACATGAGGCACA[A/C/G]GAGTCAAGAGAGAAA	54476
rs547443303	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5627362	TGTGGCAGCCTTGGC[C/T]CTCCTTGTGAGGGCC	54476
rs547454851	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663541	GTGAGCTGAGATTGC[A/G]CCACTGCACTCCAGT	54476
rs547471074	snp	C/T	0.000399281	0.0141238	missense	RNF216	GRCh38.p7	7:5622885	TGCCGCGGCTGGGGG[C/T]CAAAGTGCATGGGCA	54476
rs547476911	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750743	CTCATAAATGTGAGA[A/C]TCTTACTCTCCTTAA	54476
rs547477050	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5708751	TGCCCAGCTCTTTTT[C/T]GGCCTCAGCAGCTCC	54476
rs547481749	snp	A/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5732351	AACCAGACACGGACT[A/T]GCTTTAAAATGGTCT	54476
rs547498585	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5722459	CAGTGGTGCGATCTC[C/G]GCTCACTGTCAGCTC	54476
rs547511118	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5751061	GCCTCCACCCAAACT[A/C]TGGGTATTACCCTCC	54476
rs547512855	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5643395	ACCAGGCAGGAAACA[C/T]AGCCCCGCAGGATGT	54476
rs547517880	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5658187	CTCCATGCAACCAAT[A/G]AAGTGCTTCTCCTAC	54476
rs547518901	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5653324	AGCCAGGCGCGGTGG[C/G]TCACACCTGTAATCC	54476
rs547527254	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5647718	CTGAGAATCATTCTA[C/G]ACTCCTTCCGCTCTT	54476
rs547529977	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5684837	CCTCACATTTTTAAG[C/G]TGATGAAAAGAGAGG	54476
rs547544611	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5686084	AAAAATTAGCCAGGC[A/G]TGGTGATGCACGTCT	54476
rs547547172	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5658512	AAATACAAAAATATA[G/T]CTGGCTGTGGTGGTA	54476
rs547561563	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5727882	TACCTCATCCTGGCT[A/G]GTGAGATTTTCCATA	54476
rs547610873	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5729816	ACTACTAAAGAAGTA[C/T]AGTTGGGGATTTAAA	54476
rs547618289	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5631600	GAATCCCATGGGGGT[C/T]CCATGACATTTTCTC	54476
rs547651826	snp	A/G			utr-variant-3-prime	RNF216	GRCh38.p7	7:5621686	ACACGACAAGGACAA[A/G]GCAGGGCATGAGGAG	54476
rs547653042	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5735622	AGAAATCATCCAGAA[C/T]GCATCTCAGAGACAA	54476
rs547653476	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668785	GCCTGCCCTTCCAGG[A/G]CTTCATGCCCTTCAT	54476
rs547656798	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5632101	TCTGCATGGCTCAGG[C/T]TGGGTTGCTGGGCTC	54476
rs547665206	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5645558	ATCTCAGCTATTGTA[A/C]TTTTGGGGTACAGAA	54476
rs547669309	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5731071	CTCCTCTGAAGTTTA[C/T]GTATCAATTGGGTGT	54476
rs547673386	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5751585	CTTTAATTCTTACAC[A/G]GGAAAGGTGGCCTGA	54476
rs547684065	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5775933	GAAGATGACATGCCC[A/G]TGTCACACCAGGCCT	54476
rs547685294	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713353	AATGAGGAAGATCTC[C/T]TGAACAGCTGGACCA	54476
rs547685369	snp	C/T	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5707470	ACTGATTTTTATGTG[C/T]TAATTTTGTATCCTG	54476
rs547692489	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5769280	GCGCCACCACGCCCA[C/G]CTAATTTTTGTATTT	54476
rs547708820	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676749	ACTGGGAGAGAAAGA[A/C]AACTCCTAAACATAC	54476
rs547716211	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5642533	TTTTTTTGAGACTCA[C/T]TGCAACCTCCATTTC	54476
rs547718994	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5771688	CCTAGTCCCAGCTAC[C/T]CAGGAGGCTGAGGTG	54476
rs547774586	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5696922	ACTCCCTTTCAAGGA[C/T]CTACAAAATTCACCC	54476
rs547786659	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621336	TGCGCCACCTTGTCC[A/G]GCTAATTTTGTATTT	54476
rs547790673	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5711110	ATGGCTTAGAGCGTA[A/T]TTGTCTAGGTGGATG	54476
rs547792073	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5694991	ACTGTATTTCTATTA[C/G]TTAAGGCTTCTGTGG	54476
rs547792514	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5716501	TAATGATTTTTAACA[C/G]GAACATCTATTATCT	54476
rs547817523	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621530	ACGGTGCCCGCCTGC[C/T]CCAGGCACCTTGGGT	54476
rs547821175	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656751	CTTCCGTCTTCCTTT[A/G]TTCATTTTCTGCTGC	54476
rs547836228	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5635845	TTTGGAAAAATGAGT[C/G]TCTCTTAACCAAATG	54476
rs547839435	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712206	AGCTACAGTCTGGGC[A/G]CGGTGGCTCACGCCT	54476
rs547859856	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5756059	AAGTCACGAGCGGGA[C/G]AGGTGGAGGTAATCG	54476
rs547868734	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5690309	TCTAGCCTGGGCAAC[A/G]AGAGTGAAATTCCAT	54476
rs547890724	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5685437	AGGGAGGATTGTTGG[A/G]AGGGCAGGGCTATAG	54476
rs547904195	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5779083	AATGCAAATATAATG[A/G]TATCAGGTATGAGAA	54476
rs547904824	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5722771	TCACGCCTGTAATCC[C/T]AGCACTTTGGGAGGC	54476
rs547909978	snp	A/C	0.00199481	0.0315187	intron-variant, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711590	CTGCCATCTCAGTAA[A/C]CATGTCAACCGTTAC	54476
rs547932948	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5721438	ACTAGTGTACTATGT[A/G]AATATACCACAATTT	54476
rs547939337	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5656023	CCTGTAATCCCAGCA[C/G]TTTGGAAGGCTGAGG	54476
rs547945694	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5731251	AGAGATGTAATAAAT[G/T]AAATATAAAAGACCT	54476
rs547946861	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5763940	ATGGCTGTAATCTAA[A/G]CACCTTGGGAGGCCG	54476
rs547947499	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5740280	TACAGGCGCCCGCCA[C/G]CACGCCCGGCTAATT	54476
rs547961963	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5769833	CTTGAGGTCAGGAGT[C/T]TGAGACCAGCCTGGC	54476
rs547979517	snp	A/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667320	TACTATAGGTCACAA[A/T]CAAAAAAGTTTAAAA	54476
rs547991134	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5655641	AAGACAAGACCAGAC[C/T]ATGTAGCTAGATATG	54476
rs548023749	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5693772	CCAAATTAGGAAGCA[A/G]GAAGGCTGATGTCTC	54476
rs548027840	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5688208	TGATTAGTCTTCTTT[C/T]GATTACTTTTATATT	54476
rs548031905	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620430	GCTGGCTGGTCTGAA[A/G]ACCCCCAGTGCTTCT	54476
rs548035655	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5735961	AGCCAGACATGATGG[C/T]GCATGCCTGTAATCC	54476
rs548037785	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5700977	CCCCTCCTGTACTCA[C/T]TTCTTCTGAATGTCA	54476
rs548040129	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5688834	TTGCTCTTAATAATA[C/T]GATACGAATTCCCAA	54476
rs548046155	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677254	TCAGCCAAGGAGTCG[C/T]TATCTGCTGTTGTCT	54476
rs548078449	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5694594	CAAATCTCAGTTCTT[C/G]TTTATAGGAAAACCT	54476
rs548078524	in-del	-/A			upstream-variant-2KB	RNF216	GRCh38.p7	7:5782352	AACCCTCCATCTCGA[-/A]AAAAAAAAAAAAGTA	54476
rs548079828	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5626727	TGCAGCAGGAGGGCC[A/G]TGGGCCTACACCTCT	54476
rs548086181	in-del	-/TATT	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753336	CTGGGAATAAATGTC[-/TATT]TTATTTAAATTGTTT	54476
rs548091100	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667953	CAGCAGAAGTGCTGG[C/T]TCCAGGGTACAGCGC	54476
rs548110105	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5725591	TGCGGTGGCTGACGC[C/T]TGTAATCCCAACACT	54476
rs548113463	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF216, RNF216-IT1	GRCh38.p7	7:5662381	CATGAAAGTGTTCCA[C/T]AGTCACTCCCTCAAC	54476
rs548152606	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671482	AGGCTGATGGGGTGA[A/G]CGCTATTCCAATCTG	54476
rs548158143	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5778766	TTATTATTTTTGAGA[A/C]GGAGTCTCGCTCTGT	54476
rs548162611	in-del	-/AAAA	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5646692	GCGAGACTCCATCTT[-/AAAA]AAAAAAAAAAGAAAG	54476
rs548165727	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5721744	GGTGGGTGCAAATGT[C/G]CTGTATGATTTTCAA	54476
rs548202064	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5684013	TGTGTGAAGACCAAG[A/G]CAGCAGCAAGTTGAT	54476
rs548208039	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5683473	TCCTGAGGTGGGTCC[C/T]GTATCACCCCCATCC	54476
rs548217069	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768786	CCTGCCTCACCCTCC[C/T]GAGTAACTAAGACTA	54476
rs548217193	snp	A/C	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5765552	GGAGGACTGCTTGAG[A/C]CCAGGAGTTCGACAC	54476
rs548222929	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5641673	TAAAGTACCCTGGCA[C/T]AGTGCCCAGTACTCA	54476
rs548225755	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5744806	GGTGAAACCCCATCT[A/C]TACTAAAACTACAAA	54476
rs548250361	snp	C/T	0.00557542	0.0525036	intron-variant	RNF216	GRCh38.p7	7:5772907	CCTCACCCTCCCGAG[C/T]AGCTGGGATTACAGG	54476
rs548253634	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5769086	TGTGAAGGAGGTAAA[A/C]TAGTTTATTAGACAC	54476
rs548258122	snp	C/T	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5745136	ATTAGCAAATGGAAT[C/T]CCCAGCAGCACATTA	54476
rs548262909	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678222	GCCTGCTGTAACTTT[C/T]AGCTCCTCACCAGAC	54476
rs548282313	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5719343	ATTGCATCACTGCAC[C/T]CCAGCCTAAGTAACA	54476
rs548296571	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5705325	TTCCAGTTTTGTAAA[C/T]AGCATCATCAACTAC	54476
rs548297605	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5762409	AAGCCTGTAATCCCA[A/G]CACTTTGGGAGGCTG	54476
rs548299226	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5764229	AAAAAAAAAAAACAG[A/G]TAAGTATCCATTCAA	54476
rs548324862	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5661215	AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACTG	54476
rs548347933	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5702310	AGGTGCTTCTACCAT[C/T]AGCATCTGACATGAG	54476
rs548366641	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5730442	TGCTTTGTAGGATTA[A/C]AGATATGGAGAATTC	54476
rs548373505	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5634072	CTGACTGTTCCCAAA[A/C]TAACCATTTGAGCGC	54476
rs548375284	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5644140	GAATTGTGGTTAAAT[C/G]AACATTCTTGCACAA	54476
rs548375923	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666108	GAGGCAGAGCTTGCA[C/G]TGAGTGGAGATCACG	54476
rs548404769	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5624936	GCTGCTGCCTCAGGA[C/T]AGACCACCCGTGATG	54476
rs548431405	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5772782	GATATTCCTTTTTTT[-/T]TTTTTTTTTTTTGAG	54476
rs548446030	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5720313	ATGAAGATAAAGACC[C/T]TCTCATGCTGATCCA	54476
rs548451283	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620744	GGGTTGAGGCCAGCA[A/C]CTGTCTAGGGCTGTT	54476
rs548472273	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676074	GGCTAGAGTGCAACG[C/T]GATCTCGGCTCACTG	54476
rs548482551	snp	A/G	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682330	TCTAAAAGGGCAGCC[A/G]TGGAGCACATGTTAC	54476
rs548489157	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754724	ACACAATCTTGGTGT[A/G]CCCAATGAAAAAGTT	54476
rs548516904	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5645244	CCTACTTGGAATTCA[C/T]TCAGCTTCTTGGATG	54476
rs548531981	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5729108	TGGGGGATGGATGGT[C/T]GTGTGACCTGTCCCA	54476
rs548533015	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665565	CTAATGCTGCCCCCT[A/G]GGGATGGAAAGTTAC	54476
rs548534368	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5749764	TGAGTTCGTACTATC[A/G]GACTAAATATCCAAA	54476
rs548534638	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5651479	TCAAGCGATCTACCT[A/G]CCTTAGCCTCCCAAA	54476
rs548539132	in-del	-/TTCTTTT			intron-variant	RNF216	GRCh38.p7	7:5715734	CCAATCACCAACTCA[-/TTCTTTT]TTTTTTTTTTTTTTT	54476
rs548546128	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5755614	GCAAATAATGTTTGA[A/G]ATACATCCATACTGC	54476
rs548555175	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5704688	CAGCCCACAAATAAG[C/G]ACAGAAGATTAGGCA	54476
rs548595003	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5710375	AAAACTTAAAAACAA[A/C]AACAAAAACAAAAAA	54476
rs548597451	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5634555	GCTGTGGCTGGGAAG[A/G]GCAGGGAGGCAGGAC	54476
rs548598878	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5629930	TCTTGGACTTGGGAT[A/G]AGTGACAGATGGGGT	54476
rs548618558	snp	A/C/G/T	0.000134435	0.0081977	intron-variant	RNF216	GRCh38.p7	7:5725311	ACACTGCCACCAACA[A/C/G/T]AGTTTGCATTACCTT	54476
rs548626718	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5778094	GCATTTGAGTTATTT[A/C]TTTTAAACCACAAAT	54476
rs548639230	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5743763	AAGAAAGGAGATGGT[A/G]AATCTCAGGCTTTAG	54476
rs548642903	snp	C/T	0.00020112	0.0100259	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5729588	GTCAAAAAAGTCTAT[C/T]TTAGGCAACTGAAAT	54476
rs548666596	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5734468	GATAAATTATTGAGC[C/T]GTGCATCTTTACTTT	54476
rs548669223	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5771452	AAATTCAGAATGAAA[A/C]GGCAAGCCACCAGGA	54476
rs548682464	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5731605	ACAGTAGTGCAGACA[A/G]AGTGGGTGGGGTACA	54476
rs548698199	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5655329	AGAACATATCTGAAA[C/T]GTCTTTTGAAAAGAC	54476
rs548699951	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753282	ACTGCCAATTTCTTT[A/G]AAGTGAAATAATGGT	54476
rs548703375	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5735118	GCCACTGCACTCCAG[C/T]CTGGGCAAGAGAGTG	54476
rs548706551	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5763112	ATATGAGAGTAATGG[A/G]GACAAAAAAAACAAC	54476
rs548744335	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5710903	GCGACTGTTGTGACA[A/G]TTGTTATAGCAACAG	54476
rs548745948	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5644547	GTCTCACTCTGTCAT[C/T]CAGGCTGGAGTGCAG	54476
rs548749435	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5730138	AAAAGAAAAAAGATA[A/T]TCCACTCTGGGTAAT	54476
rs548796324	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5758232	AATTTTGAAATGATC[A/G]TAAATACAAGTTATA	54476
rs548798477	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5633521	TTCAGGCTGCAGTGA[A/G]CCGAGATCACATCAC	54476
rs548801544	snp	A/T	0.00119737	0.0244387	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5777627	ACCACAGGATGGTGA[A/T]GCTATTAAGGAAGAA	54476
rs548815539	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5714906	AGAGAACCCACATAA[A/T]CACATACATCAGGTA	54476
rs548826821	snp	A/G	0.0368353	0.130617	intron-variant	RNF216	GRCh38.p7	7:5687404	CACCTCAAAAAAAAA[A/G]AAAAAAAAAAGAAAA	54476
rs548829088	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5732901	TTAGATAGTTGTTGC[C/T]GCCTTCATCCAACTG	54476
rs548835238	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5633843	AAGTGAGGTAGAATT[C/T]ACCAGAGAGGTTTTA	54476
rs548835794	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	RNF216	GRCh38.p7	7:5783193	GGAGTGCGGTGGCAC[A/G]ATCTTGGCTCACTGC	54476
rs548881918	snp	A/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5742389	TAAAACAAAAATAAC[A/T]CCACAGCAGATACAA	54476
rs548903956	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5738336	ACTCAGGCAATCCTC[G/T]TGCCTCAGCCTCCCA	54476
rs548910701	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5709325	GCTTCCTCCCAATCA[C/T]ATGGTGCTGTGCCAG	54476
rs548911357	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5658964	AATACTTCCATTAAT[G/T]AGTGAGCTTGAGACC	54476
rs548917854	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5718396	AAAAAACAAACAAAC[A/G]AAATGCGAGAAAGGG	54476
rs548969912	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5737617	AGACAAGGCCACTAA[C/T]GGCTCCAACAGTGTC	54476
rs548973903	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5703780	CTGATGGTCTCTCGT[C/T]GTTAGCGCTTGCTTC	54476
rs549020658	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5629168	CCACTGCACTCCAGC[C/T]TGGGTGACAGAGCAA	54476
rs549022179	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5638028	CGCAGCAGCCCCCTT[A/G]GATGGGCCCCACACC	54476
rs549022612	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5686967	GCCCAGTGCTCACCT[C/T]CTGTGTGGCCTGGGG	54476
rs549025190	snp	C/T	8.32189e-05	0.00645	synonymous-codon, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712807	GGGGAGCACCTTCTC[C/T]AGCTCACTGGTTGGG	54476
rs549038918	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5724029	ATACCTAAAACAAGA[A/T]ACTGAATCAAATGAA	54476
rs549039841	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5692283	TTACTTGTTCCTCAC[A/C]TACCAAAAGCTAACT	54476
rs549053190	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664768	CCAAACTGCCTGGGT[A/C/G]CAGTTCTTAAAGGAC	54476
rs549084919	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619642	ACTCAAATGCCATGG[C/T]CTCTCAGCCCAGGCA	54476
rs549088245	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5628489	AAATAAAAAAATTAC[A/G]CTTTTAGCTAATATG	54476
rs549091495	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713831	CATTAAACTCATCAC[C/T]TCATTTAGCTTTCAA	54476
rs549100842	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5719948	TTATTACACAGAATA[C/T]TGAAAAGATGTTTCC	54476
rs549104893	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5650094	GAATGTAGGAATGTG[C/T]CATCTCTATGAAGTT	54476
rs549110921	in-del	-/TTTTTTTCTTTTTT			intron-variant	RNF216	GRCh38.p7	7:5644820	TGTTTGCCTATTTTC[-/TTTTTTTCTTTTTT]TTTTTTTTTGAAACG	54476
rs549119748	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619920	TACTACTGGGCCTTC[C/T]GGGCCTGCTCCTGCC	54476
rs549124427	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5747152	TTCAACTGTTTCCTT[A/C]TAAAACAGAACAACC	54476
rs549130574	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5649474	TGATTGTGCCATTGT[A/G]TTCCAGCCTGGATGA	54476
rs549137199	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5737104	AATGTGGGGAAAAGA[C/T]AGAGAAATCAGATTG	54476
rs549144454	snp	A/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5695542	CGGTCTCCTGCTCTC[A/T]CTCTGCAGAGCAGAA	54476
rs549146916	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5686379	CAACCACCCTGAAGG[C/G]GGCTGGGACAGAAAA	54476
rs549149979	snp	C/T			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622452	CAGGTGCAGCCCCCT[C/T]TGCCCTTGGCCCAAC	54476
rs549153690	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5708833	AAGCCAGTCCCTCAG[A/G]CAGCCCCTTGAGAAG	54476
rs549160280	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5771830	GCCCAAAGGAAAAAT[A/G]GGGCAAACAATTTGA	54476
rs549167766	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643913	CTAGGCAAATGCCCA[C/T]ATGCCTCTGATATTT	54476
rs549215208	snp	A/C			missense	RNF216	GRCh38.p7	7:5715121	AGAACAAGTGAGCAT[A/C]TGCGCACTGCGTCAG	54476
rs549243467	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664222	AACATTATTTCCTCC[A/C]TATTGGGTCTTATTT	54476
rs549259545	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672337	GTTATATCAGTTACT[C/T]TGGTCTTTACTAATG	54476
rs549270467	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5623303	GATCAAAGCACAAAA[C/T]GTGGACACCTCCCAA	54476
rs549273754	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5727354	TATCCTGCCTTTGCA[C/T]TTACTAATCTATGCT	54476
rs549276831	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767534	CAGGACTAGACTCCC[A/C]AAAATCCAACAGCAG	54476
rs549278384	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5733191	GAATAATGGAAAGGA[A/C]AGCAGTGTCAGGAAA	54476
rs549283073	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670185	GTGAGGCACCCGCCT[C/T]GGCCTCCCAAAGTGC	54476
rs549288391	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5702160	CCTGCCGGGGGGTCA[A/G]CAGTTGCCTCTGCGA	54476
rs549326257	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5770661	AGGAAAACAGCCAAG[A/G]ATAACCAAAGCATTC	54476
rs549332442	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673722	CTCTACAAAAAAATT[A/T]AAAAATTAGCTGGGT	54476
rs549333616	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5630838	GGCACTATGAACTGA[C/T]TGCCACGCTGCAGAT	54476
rs549341758	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5649104	AAGTGACGGCCGGGC[A/G]GGCGCGGTGGCTCAC	54476
rs549357457	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5627807	TCTCCCCTGATAAAA[C/T]ACGAGGGACAAGAGA	54476
rs549357950	in-del	-/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5706218	CAGCGACACTCCATC[-/T]CAAAAAAAAAAAAAA	54476
rs549362704	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5774781	TTTTTTTATTGAGAC[A/G]AAGTTTTGCTCTTGT	54476
rs549376800	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643529	GCCCAGACTCCTGTA[G/T]TTATCTGTGCTCACC	54476
rs549395048	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781292	TTCGCGAAGTGGCGA[A/G]AGGGGGCCACCCGGC	54476
rs549396567	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5631583	ACACTACCAAGTTAC[C/T]TGAATCCCATGGGGG	54476
rs549411889	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5770919	TTCAAGCGATTCTCC[A/T]GCTTCAGCCTCCAGA	54476
rs549414591	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5752309	GAAAAATTCAAAATG[C/T]TTTCTGGCTGAGGAA	54476
rs549437153	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5680197	ACACACGCTCCCCTC[C/T]ACTTTAACACTCTGT	54476
rs549446984	in-del	-/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5723651	ACTCCGTCTCAAAAA[-/T]AAAAAAATAAATAAA	54476
rs549448609	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5771276	TTTTAGATAACTACA[C/T]ATTTAAACAGAAAGG	54476
rs549451436	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5747453	GTCTACTTATGGGCC[A/T]GGCAAAGCCTGAAAT	54476
rs549464046	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671516	GCCTTATAAGAAGGA[C/G]AGAGAGAGCCGGGCA	54476
rs549483703	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668127	ACATCTTGCAAGGTA[C/T]TGTTTATATAGCAGG	54476
rs549495325	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5741996	TATATACTATCTGTA[A/G]GAATCAAAGTAGTCA	54476
rs549496677	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674765	CTCTAGGAGGCCGAG[C/G]TTGGCAGATCACCTG	54476
rs549522902	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5658194	CAACCAATAAAGTGC[G/T]TCTCCTACTGGGATC	54476
rs549534073	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5738504	ACGAGGTCAGGAGAT[C/G/T]GAGACCATCCTGGCT	54476
rs549542998	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5706130	GAGGCTGAGGCAGGA[C/G]AATCGCTTGCACCCG	54476
rs549549146	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5632188	GTTCATGCCATTTGC[C/G]CTGGCCAGTGGGGGC	54476
rs549553974	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5657742	CCTCCCCACCCATAC[A/G]CCCAAATGACATACA	54476
rs549558236	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5761640	AAAATACAAAAATTA[G/T]CTGGGCGTGGTGGCA	54476
rs549584703	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5732277	GCAAAAATCGCGTCT[A/G]TAGGGAAAGGCCTGA	54476
rs549617261	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5658053	TAATGTGCACGCACA[A/C]ACGGCAGGGGAGCAT	54476
rs549667219	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679244	AGCTAACAAGTGGTG[A/G]GACAGGCATCTGAAC	54476
rs549673618	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673162	GCCCCACCTGCGGGC[A/G]GTACCGCACTGGTCA	54476
rs549692585	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5647090	ATCCACTGGGAGGCT[A/G/T]TTTCAGCCCTGAGGA	54476
rs549738307	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712655	ATCTGATGCAAGTGC[C/T]CAGGTAGTTTTCACA	54476
rs549755263	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5683978	TAAGGGCAAGATCCA[C/G]TAGGGGTCTTGTGGC	54476
rs549772899	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5740783	TCCTGAAGGTTAAGT[A/G]TAGTAAAGGAACCCT	54476
rs549798036	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5637010	CAGACTGTTAACACC[C/T]ACCCTCACGCTAACT	54476
rs549800411	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5642813	AAAACTTTTCAATTT[A/G]AAAAGCTATGTGCCC	54476
rs549815091	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5708408	TTGGGTGCACTGATG[C/T]CGGGTGCATATACAG	54476
rs549826769	snp	C/T	0.00597247	0.0543191	intron-variant	RNF216	GRCh38.p7	7:5736087	GACAGAGTGAGACTC[C/T]GTCTCAAAAATAAAT	54476
rs549855696	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754942	CTGAGGCAGGAGAAT[C/T]GCTTTAACCTGGGAG	54476
rs549865361	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736417	GGAGTCTCGTTCACT[A/C]AGTGCTCAGTGTTGC	54476
rs549872596	snp	A/G	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5731033	AAAATTTAAAAAGCA[A/G]TGAACATACTGATTA	54476
rs549873423	snp	A/C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678172	TGTGCCCAAATCTAG[A/C/G]TTTACTTCTGAGGCT	54476
rs549890518	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5750385	AGCAAATTTAAATAT[A/G]TGCTTTCAAATATGT	54476
rs549892424	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5657064	GTCCCCATGCGTGCT[A/G]GATTTCAGTTGCTGA	54476
rs549902622	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5731987	ATCTCAATGCATTTC[C/T]CTTTGCCGTTACTTC	54476
rs549911540	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5759866	TCGAACTCCTGACCT[C/T]GTGATCCACCCGCCT	54476
rs549928773	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5703778	ACCTGATGGTCTCTC[A/G]TCGTTAGCGCTTGCT	54476
rs549951544	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736706	CCACCCATCATCTGA[C/G]ACGTGGGGAGCGCCT	54476
rs549953262	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5716570	ATACTAGATCACGTA[C/T]CTGACTATAACTTGG	54476
rs549953468	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5722392	TTTTGTTTGTTTGTT[C/T]GTTTTGTTTTTTTTT	54476
rs549960036	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5640937	CCTGAAGAATTAAAA[G/T]AATTTGCCTATAAAA	54476
rs549969316	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5647610	AAGTGCTGGGATTAC[C/T]GGTGTGGCAGCCATT	54476
rs549985112	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5726106	ACATGGGGACACCCC[A/G]TCTCTACTAAAAATA	54476
rs549985977	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5684774	TAGTTAGGAAAAACA[A/G]AACTTTACCTTTACA	54476
rs550005018	snp	A/C			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754431	CCTCCCAAGAAGTCA[A/C]TGGGATGACAGGCAT	54476
rs550021093	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5739722	AAACACCTGGGTGGC[C/T]GGGTGCAGTGGCTCA	54476
rs550022995	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5735329	ATTTAGAAAATACAC[A/C]AGAAAACTAGGCACC	54476
rs550025512	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5640910	TATTTCAGAGGGCAC[A/G]GAGTTTTATTTCCTG	54476
rs550032022	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5684222	ATTCTCCCACCTCAG[C/T]CTCCGGAGTAGTTAG	54476
rs550036156	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5651994	TCAGCCACACAGTAC[G/T]ATACAAGTAATGGTT	54476
rs550084795	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5746496	TGCAGGGAGGGTATA[A/C]ACTCAGGCTTTTGGA	54476
rs550088293	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5685897	TGGAGCACTATAATG[C/T]ATTTCTATGTACTGA	54476
rs550096113	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5710942	GCGAACATATAAAAT[A/G]GCCAGAAATATTAAT	54476
rs550102451	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5661309	CGCCAGCATAGCTCA[A/T]GGCGGTCTCCTCAGT	54476
rs550103863	snp	A/C			upstream-variant-2KB	RNF216	GRCh38.p7	7:5782505	CAGGAGGATCGCTTG[A/C]GGCCAGGAGTTCAAG	54476
rs550108187	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5705895	CTGGGCAAGAAGAGC[A/G]AAACTCCATCTCAAC	54476
rs550175136	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5700185	GCTGGAAACCCTGCA[A/G]TGCTCTGTGCTGAGA	54476
rs550175437	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5694090	AAGTGCCAAGGAAAT[C/T]ATACCACTTAGCTCT	54476
rs550180076	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5630953	CTGAATCGGAACTTC[C/T]GGCAAACCTGACTGG	54476
rs550186141	snp	A/G	0.00119737	0.0244387	intron-variant, nc-transcript-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666680	GGTGGGGCCTCTCCC[A/G]CCTTCCTGCCGAGCT	54476
rs550204032	in-del	-/A	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5738201	GAAAACTTATTTTTT[-/A]AAAAAAGCATATTTA	54476
rs550214574	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5625430	TGGAATATTAATAAT[C/G]ATCAGTTTGGATTTT	54476
rs550238420	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5694563	GTCAGAATTAAGGTA[A/G]GTTTAAACGACAAAA	54476
rs550240262	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5760365	CTACTAAAAATACAA[A/C]ATTAGCAGGGCGTAG	54476
rs550248974	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5694926	TATAGAAAAGACAAT[A/G]TACTTTCCAAAGACC	54476
rs550272981	snp	C/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5689897	AGTGAGCCAAGATTG[C/T]GCCACTGCATTCCAG	54476
rs550286998	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5654483	TTTGAGGTCAGAAGT[C/T]CGAGACCAGCCTGGC	54476
rs550290013	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5726595	GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	54476
rs550290942	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5715977	CAAACCCCTGACCTC[A/G]TGATGTGCCTGCCTT	54476
rs550301181	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5696106	ACAAGAAAGCAGCCA[A/C]CAGCTCCAGACAAAT	54476
rs550317995	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621509	AGAAGCCAATGGCAG[C/T]GAATGACGGTGCCCG	54476
rs550328314	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5645933	ACTTGTTCATACACT[G/T]TGCTCCTGGTTTCCT	54476
rs550336208	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5721817	GGAACAGTACCTAGA[C/T]TCACCACAATATATT	54476
rs550356608	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5773646	GATCTCAGCTCACTG[C/T]AACCTCCGTCTCCCA	54476
rs550374815	in-del	-/T	0.470811	0.117228	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768665	AATGAAGCAACTTTG[-/T]TTTTTTTTTTTTTTG	54476
rs550402164	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5749613	TTTTAACCACAGCCA[C/T]TTTAAGTCTTGCTGT	54476
rs550407208	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5624482	TGAGTGGGCACAGCC[C/T]GAAAAGTTTCAGATC	54476
rs550428034	snp	A/G	0.00676609	0.0577691	intron-variant	RNF216	GRCh38.p7	7:5633468	TAATCCCAGCTACTC[A/G]GGAGGGTGAGGCAGG	54476
rs550428987	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5764007	CAGCCTGGCCAACAT[A/G]GGCGAAACCCTGCTT	54476
rs550438672	snp	C/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5769255	CCCGAGTAGCTGGGA[C/G]TACAGGCGTGCGCCA	54476
rs550438844	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5744702	TCTGGCTAGGCACGG[C/T]TGGCTTATGCCTATA	54476
rs550442461	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5774137	TAACTCTCTGACACT[C/G]AAGTCTTTTAATCTG	54476
rs550451486	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5730657	TAACAACAACAACAA[C/T]AACAACAAAGCACAG	54476
rs550459369	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768701	GAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC	54476
rs550465128	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620407	TCTGGGCACTGGCAC[A/G]GCCCCTTGCTGGCTG	54476
rs550524470	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675988	TGCTGGGATTACAGG[C/T]GTGAGCTACTGCGCC	54476
rs550560513	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5749140	TCTGATCAGCAAAAA[C/T]GCCCATGTATTTTTT	54476
rs550563569	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5693255	TAAAGGCAGAGTTAG[A/G]TAGCTGGGATAGATA	54476
rs550566376	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753994	AGTGAGACCCCATCT[A/C]AAATTTTAAAAAAAA	54476
rs550576989	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5688715	TATCCATACTTATTA[A/T]CAGGCTTGTCTTATT	54476
rs550579867	snp	G/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5730097	TAAACAGATGTATAG[G/T]ATACGCTGTATACAA	54476
rs550611062	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5646460	GCACCTTGGGAGGCA[G/T]AGGCGGGCAGATAAT	54476
rs550612885	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5688161	CAGGCTTTCACGCAC[A/G]GAACTGTGTAAAACT	54476
rs550653840	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671575	TTTGGGAGGCCAAGG[C/T]GGGCGGATCAAGAGG	54476
rs550683268	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5683295	AAAAGACCTTGCTGG[A/G]TTTTGTTTTATTTTT	54476
rs550697638	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677544	TAATAATGGCAAACC[C/G]TTACAAAGGGACCAT	54476
rs550702120	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5709921	CACCATGCCTAGCTG[A/G]GTTTTAAAATTTTTT	54476
rs550716745	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5729731	GAAGTTACCAGCCCT[A/G]TAAGACAGATGAGAA	54476
rs550730971	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5757775	ATCTTTTTGGAGTGA[C/T]AGAAAATGTTCCATA	54476
rs550751801	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5652829	GGAGGAGAGGGGAGT[A/G]GTAAGAATCATTAGA	54476
rs550769235	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5634470	ACCCTTAGCCCCCAC[A/C]CCTTGCTGTCCCCAG	54476
rs550773027	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670755	TTCCCTCTCATCTTT[C/G]TTGAGTTGTGTTTTC	54476
rs550790016	snp	C/G	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680724	CTTCTACTTGGATAT[C/G]TAAAAGGCACCCCAG	54476
rs550829602	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5724884	GCAGTTATTTCATCA[A/G]TAAGAATGACAGAAT	54476
rs550834392	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5654148	TCAGGAGAGAGGCCA[C/T]GAAGGCCCAGACAAG	54476
rs550838562	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665506	CCTGAGCCACCAGGA[A/T]TAGGTGACAAATTGG	54476
rs550853245	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681385	CTTGGCCCCAAACAC[A/G]TCACATTTTATAGCT	54476
rs550865253	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5752424	TAACAGGAAGATTTG[C/T]TTTGGATTACGCAAA	54476
rs550912656	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664123	CTGGAGGCTGGCAAG[A/G]CAAAGCACATCTTCT	54476
rs550914712	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5658311	TCCAACAATGAAACA[C/T]AGTTCAAAAGATTCC	54476
rs550918067	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5650002	CAGATAGAACCTGGT[A/G]AACAGGAAGTAGCAG	54476
rs550929763	in-del	-/A	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5740697	AACTCAAGGAATTTG[-/A]AAAAAAACAAGGGAC	54476
rs550934504	snp	G/T	0.000399281	0.0141238	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619581	TGTGCCAACAGCGAG[G/T]GTAGCAGGGCCCTGG	54476
rs550942192	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5709393	CAGCCTTTGATGCAA[A/C]TGGTTTCTGGATTTC	54476
rs550945064	snp	C/T	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5722864	CCCCAGGCATGATGG[C/T]GCACACCTGTAATTA	54476
rs550977959	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5658875	CAATAAAATTGTACA[A/T]CTGCCGCTCTCAATA	54476
rs550991041	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5639200	AGCAGGCTCTTTAGC[C/G]TCACTGCAGCCCCTT	54476
rs551012066	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782582	TGGCCAGGCGTGGTG[G/T]TTCACGCCTGTAATC	54476
rs551017302	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5737698	GGGCCCTTCCTTCTC[A/T]GCCTTGGCAGGGAAG	54476
rs551024155	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5629426	AGCTATGATTGTGCC[A/G]TTGTACTGGCACAAC	54476
rs551045472	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5757312	GGATTAGCTTATCTT[C/T]TCAGTGCACTGAATC	54476
rs551074240	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5686430	TGAGGAAAGTCAGAG[G/T]AAATGATGTGCGGAC	54476
rs551074611	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664984	GTATTTTTTAGGAGA[C/G]ACTGGGTTTCACCAC	54476
rs551077621	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5696225	CTGTCAGGAGGCCCA[C/T]GGAAAAAAAGCAGGG	54476
rs551092498	snp	A/G			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622228	ATGAGAAAGTTAGGC[A/G]GCAACAGAACAAAAC	54476
rs551124383	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5632498	CCCTGGATCAGCAAG[C/G]GCTCAAAAGAACAAG	54476
rs551140440	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5649615	CCCGTGGAGCACCCT[C/T]TCTCTAAAAAAAAAA	54476
rs551150432	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5719347	CATCACTGCACTCCA[C/G]CCTAAGTAACACATG	54476
rs551173427	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5762590	CCAGCTAGTCAGGAA[A/G]CTAAGGCAGGAGAAT	54476
rs551190452	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782069	GTAAAGTGGGTCCCA[C/T]GGCTGGGCACAGTGG	54476
rs551219503	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5741881	CTCCTTATGTACTTA[C/T]ATTGAGCTTCCGAGA	54476
rs551230823	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5729063	GACTCTCTACAGACC[G/T]TACGTCCTATCACTG	54476
rs551254198	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5748263	GTGCCCTACAGTTCA[C/T]CTTTTGAAGGAAAAA	54476
rs551256188	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675602	GCTAGGATCACATCA[A/C]TGCGCTCCAGCCTGG	54476
rs551284342	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5637703	CACCACCACCCCTGG[A/G]TAACTTTGGGATTTT	54476
rs551286536	snp	A/C	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5714424	CCACCAGGTCTGGCT[A/C]ATCTTGTATTTTTAG	54476
rs551301414	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663571	TCTGGGCGACACAGC[C/G]AGACTCCACCTCAGG	54476
rs551309536	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5737052	TTGAGAACGGGCCAT[A/G]ATGACGATGACAGCT	54476
rs551309963	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5721767	ATTTTCAACCATTTT[C/T]ATTTTCAAAGCATTC	54476
rs551317040	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5771410	GAAACACTATACATT[A/G]AAATTAAGCATGTCT	54476
rs551339856	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5771275	ATTTTAGATAACTAC[A/T]CATTTAAACAGAAAG	54476
rs551339885	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5732825	TGATCTGACATGCTA[G/T]CAGTTCTAGAGAAGT	54476
rs551351181	snp	C/G	4.09945e-05	0.0045272	intron-variant	RNF216	GRCh38.p7	7:5624006	GGCCAGCAGAAGCCT[C/G]CATGGCCTGGCTGCT	54476
rs551378086	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5628873	TTCCACAATCAGTTT[C/T]TCTGAAGCATTTGAA	54476
rs551400949	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5762121	AGGAATAAATAAAAT[C/T]CATATGATACAACAC	54476
rs551404936	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5766134	ACGAAAAATAAAAAT[C/T]AAAAAACTAGCTGCG	54476
rs551414257	snp	C/T			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622091	GCCCAGCAGGGCCAC[C/T]AGGCCTCTGTCCCAG	54476
rs551471301	in-del	-/AAATTTTAAAAAGTG	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5702726	ATTCACTATGCTTTT[-/AAATTTTAAAAAGTG]AAATTTTAAAAAGTG	54476
rs551480919	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5654341	AAATGGAACAGAATG[C/G]TGAGGGAGCTGAGAA	54476
rs551490731	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5751129	ACCCTCAGAAAGTTT[C/T]AAATGTTTCCATACA	54476
rs551498073	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5648983	TAGTTTTGTTAGTGG[A/T]CATAAAGGTAAGTGC	54476
rs551500759	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5717740	CCAGGATGCATGGTT[A/G]AATGAAAAATGCAGT	54476
rs551521912	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674725	TATAGTTGTGCAAAG[C/T]GGGGGGTCTTTAAAG	54476
rs551550489	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713419	GCAGAGCTGAGGGGT[A/G]GCCTGAAGTCAGAGT	54476
rs551568159	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5638009	CAACAACCTGTAGTG[A/G]CTGCGCAGCAGCCCC	54476
rs551583604	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5746615	GATTGGCTAGGTAGG[A/G]CATCTTGGAGCCAAC	54476
rs551593537	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5776015	TTTCATTCAAATACC[A/G]GTTGCTCATCCTAAC	54476
rs551599465	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712390	AGGCATGAGAATTGC[C/T]TGAACTCAGGAGGCG	54476
rs551604740	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5633000	TTCTGTTTTTTTTGA[A/G]ACAGAGTCGTGCTCT	54476
rs551619364	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5687349	TGCAGTGAGCTGAGA[C/G]TGCGTCACTGCTCCA	54476
rs551639259	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5726709	GTAAAAATACAAAAA[A/G]TTAGCTGGACGTGGT	54476
rs551641895	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5765183	AATGAACTTCAAGAC[C/T]GGGCATGGTGGCTCA	54476
rs551650230	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5731490	GTAAGGCTATATAGA[G/T]TGAGATAACACACAC	54476
rs551660847	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5731407	ACAGATCATGTTTTC[C/G]TATGAACAGACTCTC	54476
rs551663219	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622119	CAGCTGCCTTAAGAG[A/G]CTCTTTCAATGGGCC	54476
rs551697861	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5648194	TCACCATAACCTCTG[C/T]CCCATAGGTTCAAGT	54476
rs551700045	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5727142	TGGCTATGATGCAGT[A/G]TTTGCCTGAAACTCC	54476
rs551718239	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5771760	TGTGATCCCGCCACT[A/G]CATTCCAGCCTGGGC	54476
rs551730020	snp	A/G	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5756044	TCCCATAATCCCCAC[A/G]AGTCACGAGCGGGAC	54476
rs551747834	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5774392	GCAAGTAAGCTATGA[C/T]AGCACCATTGCACTC	54476
rs551749581	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5779596	TGTAATTCTTGTGCT[G/T]TGGGAGGCTGAGGGT	54476
rs551810513	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5756665	GCTCTCTGTTGCCCA[A/G]GCTAGAGTACAATAG	54476
rs551813972	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5652785	ACAGAGTGAGACCCT[A/G]TCCCTTAAAAAAAAG	54476
rs551826044	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5689114	TGGCACCACCATCAG[C/T]GCCTTGTGAGCCAAT	54476
rs551832874	snp	C/G	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780335	CTGCTCACCCTCTAC[C/G]TCACAGTGCTTCTTC	54476
rs551852345	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5751579	CCTCTGCTTTAATTC[G/T]TACACAGGAAAGGTG	54476
rs551883246	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711666	AAATCCTTCTTATAC[A/G]TCAGCAGTCAGGTAA	54476
rs551883366	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5746952	ACAGAATTCTAAAAT[A/G]GCTTTTTTGAAAGAT	54476
rs551894658	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679428	TTGTGAGGATGCAGG[C/T]GCTGAGCGCACTGGT	54476
rs551895230	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677810	GCAGAGACCATTAGA[A/G]TAACTAAATCAGAAT	54476
rs551896882	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5685939	ACGATGTAAAAAATT[A/C]CGGCCGGGCGCGGTG	54476
rs551927214	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5759751	ATTCTCCTGCCTCAG[C/T]CTCCCAAGTAGCTGG	54476
rs551932642	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736385	CCTCGGCCTCCCGAG[A/G]TGCCGGGATTGCAGA	54476
rs551940638	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5632154	GGTTCACCTGAACCT[A/G]TTTGAGATCTGAGTT	54476
rs551969822	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5638515	CAGTGTAGCAGATGC[C/T]AACAAATCTGAAAAC	54476
rs551974001	in-del	-/AA			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768296	TCGCTATTAGGGGGA[-/AA]AAAAAAAAAAAAGGC	54476
rs551982217	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5683537	GCATCATGACTTAAC[C/T]ACCTCATCAGAACTC	54476
rs551982218	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5689248	CTCCAGAAGCTGATA[C/T]GGCAGCATTTTGGCT	54476
rs551997941	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5765465	TGAGACTCCATCTCA[A/G]AAAATAAAAAAATAA	54476
rs552003508	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5770623	TTAAGAATAGATATA[C/T]ACTAGATGACTTTAG	54476
rs552017543	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662901	AGAGAAGCGTTCCAG[C/G]TACAGGGAATGCAAG	54476
rs552032524	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5731945	CCCGCCGGGGACCCA[C/T]GTCAAAGCCTTCTCC	54476
rs552033123	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5636381	AACTAACAGAGAAAG[A/T]AAGTTACTGTTCACC	54476
rs552033186	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5658048	CAGTGTAATGTGCAC[A/G]CACACACGGCAGGGG	54476
rs552052613	snp	G/T	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5763984	ACTCGAGGTCAGGAG[G/T]TTGAGACCAGCCTGG	54476
rs552059688	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5779115	GAATTATGTCTCTAA[A/C]GAGCTAGAATATAGC	54476
rs552086854	snp	C/T	1.64773e-05	0.00287026	missense	RNF216	GRCh38.p7	7:5761056	ACCTCTTCATTGTTG[C/T]TTCCCTCTTCCATTT	54476
rs552094104	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656191	GGAGAATTGCTTGAA[A/C/T]CCAGGAGGTGGAGGT	54476
rs552097756	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754828	AGGCCAGGAGTTCGA[C/G]ACGAGCCTGGCCAAC	54476
rs552107252	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5773166	TGATGTTATTAATAA[A/G]TAGCATGGTATTTAA	54476
rs552153305	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5727190	CAGTGTGGCGGTGTT[C/G]AGAAGGTGATCTCAT	54476
rs552161906	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712067	ATATAAACCACTCAA[C/T]AAACACGTCCCAACC	54476
rs552183388	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750372	AAATTTCCAGCAAAG[C/T]AAATTTAAATATGTG	54476
rs552212494	in-del	-/AAAC	0.156918	0.232818	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675639	AGCAAGACCCTCTCA[-/AAAC]AAACAAACAAACAAA	54476
rs552214792	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5725829	CACTGCACCACTGCA[C/T]TCCAGCCTGGGCAAA	54476
rs552221324	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676211	GAGATAGGGTTTTGC[C/G]ATGTTGGTCAGGCTG	54476
rs552248863	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5769229	TTCAAGTGATTCTCC[C/T]GCCTCAGCCTCCCGA	54476
rs552269671	snp	C/G	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5688852	TACGAATTCCCAAAT[C/G]ATGATAACAGCTACT	54476
rs552278801	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667415	CACAATAGGAAGTCC[C/G]AAGGATCACTGCCAG	54476
rs552333804	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5722748	TTTTTGGGGCCAGGC[A/G]CAGTGACTCACGCCT	54476
rs552334849	snp	A/G	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5699725	TTACACTGGACATGA[A/G]GGGCAGCAGGCTTTC	54476
rs552339959	snp	G/T	0.00835141	0.0640778	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668010	CGTTGGTATTTTAGG[G/T]CGCTGTGTAAAGATG	54476
rs552360163	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5721528	GCTGCTTATAGCCAT[C/T]TGTTGGTGAATGTAT	54476
rs552371518	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5730496	AAGATAAGAATTACA[A/G]GGAAAGATAGAAGTT	54476
rs552373052	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5651784	CTCCCGAGTAGCTGG[A/G]ATTACAGGCAAGCGC	54476
rs552378971	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5777931	AGAAACTAGGACAGA[C/T]AAGTAAGTACATCCT	54476
rs552387304	snp	G/T	0.00398564	0.0444627	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5621179	TATCTTAGTTTTTTT[G/T]TTTTTTTTTTTAAAG	54476
rs552391913	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620871	CTGAGGTCACCTCTT[C/T]AGCTGTGATGTCTAC	54476
rs552393644	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5764473	GTCAACATGGCAAAA[C/T]GCCGTCTCTACTAAA	54476
rs552410862	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5738858	AAACAACTCAGTTAT[A/C]ATAATTCTATAACCA	54476
rs552439180	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5656226	TTGAGCTGAGATGGT[A/G]CCACTGCACTCCAGC	54476
rs552454593	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5779636	CCAGGAGTTGGGCAG[C/G]ACAGCTAGACTCCGT	54476
rs552477415	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750627	AATCGCAAGGAATAA[C/G]TCTCATGCCTAATGC	54476
rs552486951	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5707839	AGCGATTCTCTCCTG[A/C]CTCAGCCTCCCAAGT	54476
rs552511080	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5640166	GCCTTCAAAAGTGCT[A/G]GCATCACAGGCGTGA	54476
rs552515657	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5644221	GGAACTGCTGGGTCA[C/T]ATGGTAATTCTATGT	54476
rs552545870	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5635161	ACTGCCTCCCAGTCC[C/T]ATGCAGTAAAAATCA	54476
rs552550324	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5644613	TGGGCTCAAGTGATT[G/T]CCCACCTCAGCCTCC	54476
rs552568238	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5682912	TGCATTGCGTTAATG[C/T]AGCATCAAAACCAGA	54476
rs552587734	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5705838	CTTGAACCTGGGAGG[C/T]GGAGGTTATGGTGAG	54476
rs552593621	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5630318	ATGCAGCTCTACCCC[C/T]ACTACCTAACCTGGA	54476
rs552633927	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5624969	TGCTTCATGAGTGGC[A/G]CTTACCTTAACCCCC	54476
rs552635498	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5630896	GACCCAGGCAATCTC[A/G]TCTCAAAGCCTGAGC	54476
rs552653597	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5720050	TAAAAATGTAAGTGC[A/G]TGGTGGTGAAGAAAA	54476
rs552655147	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670479	TACTTCCTCTTTTTG[C/T]TTATTCTTGGATTTA	54476
rs552714797	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5714524	CGGCCTCCCAAAGTG[A/C]TGGGATTACAGGCGT	54476
rs552738212	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5628488	AAAATAAAAAAATTA[C/T]GCTTTTAGCTAATAT	54476
rs552747283	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5685625	AGAGGGGAGGGGGCA[C/T]AGTGGAAAAGGAAGT	54476
rs552795299	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5778189	TGACATAGCGGGCCT[C/T]ACCTCATACCTTTTC	54476
rs552815322	snp	A/C	2.90584e-05	0.00381161	intron-variant, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711727	CATAATACCATAATT[A/C]AATATACATCTAGAA	54476
rs552827037	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5723960	ATACTTCCAGGGTCC[C/T]TCAAGATTATCTGAT	54476
rs552830436	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5723733	CATAAAAAGGACAGA[A/G]GAGGGAGAACCGTGT	54476
rs552831344	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5645111	TGAGCCACCGTGCCC[C/T]GCCTGTTTGCCTATT	54476
rs552866225	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5659074	CTAGGCTTCTGATGT[A/C]GGACACTAGCGAGAT	54476
rs552874575	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5697151	TCACCCAGCTTTGCT[C/T]GTGTCATTCTCTGGG	54476
rs552875214	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5693728	GTGTTGTTCTAAAGT[C/T]AGGCAAGACTGCCTG	54476
rs552875714	snp	C/G	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5649705	AGATGCAGAGGCGAT[C/G]ATTCTTTCACATCTC	54476
rs552877553	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5734634	ACCCAGGTAGAGTCT[A/G]TCGTTGAAAAATAAA	54476
rs552878789	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5705399	TCCCCACCTTCACAT[A/G]CAACATATCACCTTC	54476
rs552891846	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5714136	CCTGGCTAATTTTTG[C/T]ATTTTTAGCAGAGAT	54476
rs552919098	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5623384	CTCCACAGTGGCACC[C/T]TGGAAGGTGGCACGT	54476
rs552935074	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5745140	GCAAATGGAATCCCC[A/T]GCAGCACATTACTAC	54476
rs552936520	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5638923	ATGAGCCACTGCACC[C/T]GGCCAGCAAGCAGCT	54476
rs552949232	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5708330	ATTGAAAGTGAGGTA[C/T]TGCAATCTCCTACTA	54476
rs552980416	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5654484	TTGAGGTCAGAAGTT[C/T]GAGACCAGCCTGGCT	54476
rs552990067	snp	G/T			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713260	GGCAGGGACTCAAAG[G/T]AATAAACTGAAAACA	54476
rs552995765	in-del	-/AGA	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754033	GTGACCTAAAAGAAG[-/AGA]AGAAGAAAGAAACGA	54476
rs552998580	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5765816	AAAAAATTAGCCAGG[C/T]GTGGCAGTATGTGCC	54476
rs552998907	in-del	-/TT	0.0213279	0.10104	intron-variant	RNF216	GRCh38.p7	7:5774762	ATTCCAAGTTACTTT[-/TT]TTTTTTTTTTATTGA	54476
rs553006480	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5627996	CCTGCATAGGAGCGC[A/G]AGCCCAGGTTTCTGA	54476
rs553025517	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5689465	CTTCTGTTGTCAAGT[C/G]ATCAATAATTTCCCA	54476
rs553055874	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5728168	ACCCCTTTCACCAAA[C/G]TCCTATGTGGGTCTG	54476
rs553065659	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5737918	CATGATGAAACCCTG[C/T]CTCTACTAAAAATAC	54476
rs553068617	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5638143	ACCACCTGCCCCTGT[A/G]GTAACTTGGGTCTGT	54476
rs553073045	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5777345	TACATCAACAGATAA[C/T]TGAAACAGAGCTCAG	54476
rs553115682	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5694691	GCAGAGATGTGTATG[A/G]TGGCCATGCCCTTCA	54476
rs553131493	snp	A/C	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780572	CGTGGTGGCAAATGC[A/C]TGTAATCCCAGCTGA	54476
rs553137919	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5758496	TCCCCTTATTTGCAG[A/T]TTTTCTTCCACTTGT	54476
rs553138703	snp	A/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5709636	CATAGACAAACAAAA[A/T]CATATGTGGTGTTCC	54476
rs553146464	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5737163	CATAGGAGACTCCAT[C/T]TTGTTCTGTACTAAG	54476
rs553164872	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5762344	CCTGGCCAACATGGT[A/G]AAACCCCATCTCTAT	54476
rs553181644	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5691311	GACCCACTTTACTCA[C/T]TGCTCCTTACTTCTC	54476
rs553181814	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5757503	CTTCATTTTTAAGCC[C/T]ATTTTCACTAGGTAC	54476
rs553193767	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5729079	TACGTCCTATCACTG[A/G]TAACTGAGCCACCTG	54476
rs553197567	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5774957	TTTCGCCATCTTAGG[G/T]TGGTCTTGAAATGCC	54476
rs553208255	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5648794	AGTTAAATGATACCA[C/T]GAGAAACCAGCCAAC	54476
rs553218912	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5752593	GTAAGATACACTATA[A/T]TGTTGTAGCAATGAC	54476
rs553219140	snp	A/C	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780808	CTTAGGGATTTACAG[A/C]GCCCTGTCGGATTTG	54476
rs553271300	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5646607	CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAG	54476
rs553275430	in-del	-/A			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669730	AAAACCCCATCTACT[-/A]AAAATACAAAAATTA	54476
rs553288886	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713502	CTCAGTTTCAGAATG[C/T]TGGAAAATGGGCTCA	54476
rs553289305	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5694649	AGGCCCACTTGTGGC[A/G]CAATTTGAGGACCTG	54476
rs553301349	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5751934	GGCTCACGCCTATAA[C/T]CTCAGCACTTTGGGA	54476
rs553311391	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5760710	TTTATAATCACCACG[A/C]CTTCAAAAACTGATG	54476
rs553338627	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667939	CATCCTGAGTCATTC[A/G]GCAGAAGTGCTGGTT	54476
rs553343323	snp	G/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5702537	AGGCAGGGTGGGAAG[G/T]GAGGCAAGCAACATT	54476
rs553345181	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	RNF216	GRCh38.p7	7:5781793	GCCTAGTCGCGCCTG[C/T]ATCCGGGCTCTCCGC	54476
rs553351652	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5736877	AGTGAGGAGCCCCTC[C/T]GCCCGGCAGCCGCCC	54476
rs553381960	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5680288	GTTCCTTTGTCCCCC[A/G]CCCTGCCCCCAGCTA	54476
rs553401172	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5761255	CTTAAGAAAACATAT[C/T]CAAGGAGGTGGGTCA	54476
rs553407231	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5690684	CAAACAGAAGTCCAC[A/C]AAGGCAGTGGGAAGT	54476
rs553472469	snp	C/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5627916	TTATCACTAAGCTTC[C/T]GTGATAAATCCCAGT	54476
rs553481415	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663767	GCCGGGTGTGGTGGC[A/G]CACGCCTGTAGTCCC	54476
rs553488820	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5717886	CTCCCAGGCTCAAGA[C/G]ATCCTCCCACCTCAG	54476
rs553504911	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5751317	CAGGTCCTGGGTGAA[A/G]GCCTAACAAAAAGGG	54476
rs553524382	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5761955	ATGTACATTCCCTGT[A/G]ACTTAGCAATTCCAC	54476
rs553526299	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5766967	ATAAAATTACAAGCC[A/C]AAATGAGGATGCTAC	54476
rs553529587	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673188	GGTCACCAGCACCAC[C/T]CCAAGCGGGGGAAGT	54476
rs553532811	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5695563	CAGAGCAGAAGACAC[C/T]GCAGCTATAGACAAG	54476
rs553533771	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643096	AAAAAAAGGCTCTCC[C/T]AAAATGGACAGAGGA	54476
rs553536998	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5755787	TTTGGTGTACTCATT[G/T]TAGCTGGATACATTC	54476
rs553546296	snp	C/G			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681560	CACCAAGGACAGTGT[C/G]TTCCTCCTCCTTGAT	54476
rs553551520	snp	A/T	0.000798403	0.0199641	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622234	AAGTTAGGCGGCAAC[A/T]GAACAAAACCCCCGC	54476
rs553560079	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679702	ATGGAATGTGCTACT[C/G]CAAGGAACAATTAAA	54476
rs553569310	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5648677	AGCTTGCAGTGAGCC[A/G]AGATAGCGCCACTGC	54476
rs553583275	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673222	TGGTTATTGAGATTC[C/T]TCTATGAAGCCACAA	54476
rs553590834	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5692249	CTTCTAAGCAGACAA[A/G]GATTTGCCACTAAGC	54476
rs553618681	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5637423	TTTTTAGGGGTCTCT[C/T]ATCCCAGCTTCCCAC	54476
rs553621566	snp	G/T	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674223	TTAGTAGAGACGGGG[G/T]TTCACCATGTTGGTC	54476
rs553649050	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668191	CATTCTCATAAAAAT[C/G]AAATCCCTTCTCAGA	54476
rs553666148	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5637808	GGGCTCTCGAAGTGC[G/T]GGGATTACAGGCATG	54476
rs553688117	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5634031	TTTTCACAAATCAGA[C/T]ATGAACAGTAATCAG	54476
rs553705257	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668967	GGCTCTTATCCAGCC[A/G]AAATCTAGTCATCTC	54476
rs553712798	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5695211	CCTGGGTCCGGCTTA[C/T]AAATCTAACATCTAC	54476
rs553727767	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5718137	TATAATCCCAGCACT[A/T]TGGGAGGCCAAGGTG	54476
rs553732385	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5693086	CACAACGGGATTCCA[C/T]GTCATTCTTTTAAAC	54476
rs553744759	in-del	-/CTT	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5710464	CTTTCACTGGCAGAC[-/CTT]CTTTGAAACCTTACC	54476
rs553753409	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750419	TAGTCAGGCAAACTG[C/G]TCTTACTGTGATTAT	54476
rs553772639	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5726815	GTGAGCTGAGATCGC[A/G]CCACTGCACTCCAGC	54476
rs553779582	snp	C/T	0.00159617	0.0282053	intron-variant, downstream-variant-500B	RNF216, RNF216-IT1	GRCh38.p7	7:5662197	CAGACCTGAGGATAC[C/T]CTTTCTTACTGGTAA	54476
rs553791162	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5626850	AGTATGTAAAGGATG[C/T]AGCCCAAAGTAAATG	54476
rs553800022	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5726350	GGGCTGGTGAGTCCC[A/G]TTCTGTAGGCAAATC	54476
rs553815267	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5756262	CCTTCCCAGCAATAT[A/G]GAACTGTGAGTCAAT	54476
rs553816723	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5661758	CAGTGAGCTGAGATT[G/T]TGCCACTACACTCCA	54476
rs553841158	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5745525	AAGACAGATCAGATG[C/T]ACGTTTTCAAGAAAT	54476
rs553843653	snp	C/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780902	CTTGGATCCCTGGTC[C/T]TGTTCCACCGGGAGC	54476
rs553846543	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5646777	TGTATTAGCTTAGTG[A/G]TCAATGCCAGGAAAA	54476
rs553852594	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5765889	CCCGGGAGGCAGAGG[-/T]TTGCAGTGAGCCCAG	54476
rs553869292	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5716963	ACAATATTTCTTAAG[C/T]ATGACTCAAAATGTA	54476
rs553876468	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5722976	CAGCAACAAAAAAAA[C/T]CAGTTTTTGGTATTA	54476
rs553881820	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5684346	TCTCCTGACCTCGTG[A/T]CCCACCTGCCTTGGC	54476
rs553888717	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5727376	ATCTATGCTTATTAT[C/T]GAGTGGCCAAGTCTA	54476
rs553917592	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5764983	GCTGAGGCTAGAGGA[C/T]TGCTTGAGCCCATGA	54476
rs553920240	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656086	CCAGCCTGGGCAACA[C/T]GGTCAAACCCCATCT	54476
rs553920707	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665940	GGAGGCCGAGACAGG[C/T]GGATCCCGAGGTCAG	54476
rs553922974	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5775013	CACTCACCAAAGTGG[G/T]GAGATTACAGTCGTA	54476
rs553951144	snp	A/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5740457	TATCACCACTAATAG[A/T]ACTTTGTTGGATGAC	54476
rs553993955	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5752434	ATTTGTTTTGGATTA[C/G]GCAAACTGATTATAT	54476
rs553994142	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5720334	TGCTGATCCACACTT[C/T]CATTTAATGAATATG	54476
rs554003858	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5706630	TTGACGAACATGTCA[C/G]TAAGTGGTTTCCATC	54476
rs554004983	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5739986	CCAGCCTGGGTGACA[A/G]AGTGAGACTCGGTCT	54476
rs554006542	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5701193	GACTAAAGGAGAGCT[A/G]TCATTTCTTATAGAA	54476
rs554026914	snp	C/T	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5725887	GGTAAAATAAATAGG[C/T]AGCATTTCTTTATTT	54476
rs554028053	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5631872	TCCATTGTAGAAGGT[C/T]ACGCTCTGCCCCCAC	54476
rs554048158	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5685487	CAAGACACTAAGGGA[C/T]GCACACTAAACATTA	54476
rs554066300	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5727917	GATGACTCTCAAAGT[C/G]CTATCACCATAAAAC	54476
rs554091822	snp	A/G	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5651626	GAGAAAGAGATTTCA[A/G]TATTACTTCGGTCAT	54476
rs554100933	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5754971	AGATGGAGGCTGCAG[C/T]AAGCCAAGATCATGC	54476
rs554139285	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5710490	CCTTACCAGGAAATG[C/T]AGTTCCCAGCTCCTT	54476
rs554159555	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5635358	TAACACGCCAAAGCC[A/G]GCTGTGGAAGCTGGG	54476
rs554162112	snp	C/T	0.000248174	0.0111367	intron-variant	RNF216	GRCh38.p7	7:5716673	GTAAGAGAAAACAGC[C/T]CATGAAAATGCCCAG	54476
rs554175465	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5639665	AGGTTTCACCATATT[A/G]GTCAGGCTGGTCTTG	54476
rs554182627	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5684298	ATTTTTAGTAGAGAC[A/G]GGGTTTCACTGTGTT	54476
rs554261637	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5691756	ACCGGAGAGTTACTA[A/G]TGTATGAAATTGAGG	54476
rs554285494	snp	A/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5739060	GCCACTGGCTTGGGA[A/T]GGGGATGGGGAGTGA	54476
rs554317345	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5661378	GTAGGCTTAGGTTTT[C/T]TGTTAAAGAAATAAA	54476
rs554318985	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782949	TTATACCTGGAATCC[A/G]AACATTTTGGGAAAT	54476
rs554322597	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5734755	CCTGAACCTGGGAGG[C/T]GAAGGTTGCAGTGAG	54476
rs554325704	snp	C/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5699879	CTCTGTATTCTTTAT[C/G]TTTGTCTCAAAGTCA	54476
rs554329131	snp	A/C/G	0.00676609	0.0577691	intron-variant	RNF216	GRCh38.p7	7:5762433	GAGGCTGAGATAGGC[A/C/G]GATCATGAGGTCAGG	54476
rs554336895	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5699169	TGAGCTTATCTATAC[A/C]CTACCTGTTCACTCA	54476
rs554365713	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666291	GATTGTAAGTGCTGA[A/G]GAGAAAAAAATAAAG	54476
rs554379760	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5660932	CTAGCTCCATGCTCC[C/T]GAAGCCTTAGGTTTT	54476
rs554389334	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5642217	CAAGGTTCTGTTTTG[-/T]TTTTTTTTTTTTTGA	54476
rs554389445	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5693454	GTTCCCTGCTGATGG[A/G]TATTGCATTGGATTT	54476
rs554408778	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	RNF216	GRCh38.p7	7:5783381	GTAATCTACCCACCT[C/T]GGCCTACCAAAGTGC	54476
rs554409637	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5621005	GGCACTGTCGTTCAG[A/G]CTAGTAGCAAAGTTC	54476
rs554425712	snp	C/G			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622763	CTTCAAGCTGACTTA[C/G]GATGCAATGGTACAG	54476
rs554432850	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753718	AAAAAAAGCATTGGC[C/T]GGGAGCAGTGGCTCA	54476
rs554450677	snp	C/T	0.00676609	0.0577691	intron-variant	RNF216	GRCh38.p7	7:5694137	GTCAGTTTTACACTA[C/T]TGAGAAAAGAAGAAT	54476
rs554454051	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5758874	TGTTGGGAAGACGCA[A/G]TTGTATTTAGCAATG	54476
rs554476095	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5710227	CAGTCAGGCGTGGTG[A/G]CGCATACCTGTGATC	54476
rs554478553	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5715604	CATAAGGAGTGTGAA[C/T]GGGTCTATCGAGGTC	54476
rs554494553	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768270	AGCCTGGGAAACATA[G/T]TGAGATCTTGTCGCT	54476
rs554512423	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682207	ACCTACGTGCCAGCC[A/C]ACACTGACTTTTTCT	54476
rs554524073	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5775688	CAGCCTGGCCAACAC[A/G]GTAAAACCTGTCTCT	54476
rs554532215	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5637759	TTCCAAAGCTGGTCT[G/T]GAACTCCTGAGACTC	54476
rs554535652	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5697713	ATCTTTACAAGCAAT[G/T]TGAGGTGCTTAGGAT	54476
rs554544438	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5651423	TTTTTGTAGAGATGA[A/G]GTTTTACCATATTGC	54476
rs554548988	in-del	-/A	0.428182	0.17536	intron-variant	RNF216	GRCh38.p7	7:5733664	AGGAAAACATTAACC[-/A]AAAAAAAAAAAAAAA	54476
rs554574498	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5721445	TACTATGTGAATATA[A/C]CACAATTTATTATCT	54476
rs554574976	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5773723	ACACATGCGTGCCAC[C/T]ATGCTGGTTAATTTT	54476
rs554580737	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5763359	TTGAGGGCTAGGAGC[A/G]ATGGCTCACACCTGT	54476
rs554582770	in-del	-/T	0.294576	0.245994	intron-variant	RNF216	GRCh38.p7	7:5772776	GAAAAAAGATATTCC[-/T]TTTTTTTTTTTTTTT	54476
rs554603579	snp	A/G	3.77458e-05	0.00434413	intron-variant	RNF216	GRCh38.p7	7:5739258	ACCACCACAAAAAAA[A/G]CATGGTAGTATACTT	54476
rs554608635	snp	A/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5639864	TCCTGGGTTCACGCC[A/T]TTCTCCTGCCTCAAC	54476
rs554611253	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5692912	TCAAAAGCGATTCAC[C/T]GCTACCCATTTCTTA	54476
rs554617438	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619832	CCCAATGTGGGCCTT[A/G]GTAGCCGCCCTAGCG	54476
rs554656063	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620055	CTGGAGGGAGCAGAG[C/T]GCACAAACATTTATT	54476
rs554663319	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5629566	AGAAGCGGCGTCTTG[C/T]GCCTGTAATCCCAGC	54476
rs554702065	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5623916	GGCCGCGTGGGTGAA[A/G]TCAGGTCTATAGCCA	54476
rs554729977	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5771974	CGTGGTGGCTCACGC[A/C]TGTAATCCCAGCACT	54476
rs554743171	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5758541	AGCAGGACTGCACGA[A/G]ACTTTCAGGAGCCTA	54476
rs554750622	snp	A/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754119	GTTTTTCTTTTGTGT[A/G]GTGTGTGTGTGTGTG	54476
rs554762662	snp	A/G/T			intron-variant	RNF216	GRCh38.p7	7:5689075	GGCTGCCGATTCTGT[A/G/T]AAACAAAATGATATC	54476
rs554768141	snp	C/T	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5710329	CGTGCCACTGCACTC[C/T]AGCCTGGGCAACAGA	54476
rs554812610	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5724915	TTTGGAGAAACGTGG[C/T]TATTAGCCATTCTCT	54476
rs554814217	in-del	-/C	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5742996	GGCCAGGCGTGGTGG[-/C]TCATGCCTGTAATCC	54476
rs554863560	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5777257	GGTGAGCACTTCTCA[A/T]TTCTCCTGATTCATA	54476
rs554863987	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676423	CGGCAGTTGCAAAAA[A/G]TATGATTCTGAACCA	54476
rs554879716	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5630749	TAGTTAACATGCACT[C/G]AGAGATTACTATGCA	54476
rs554896741	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5749243	GCAACCTCCATCTCC[C/T]GGGTTTAAGCGATTC	54476
rs554900319	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5762980	GTTAAAGCCAAGACA[C/T]TACATCTCCATGGAC	54476
rs554902406	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5772332	CCTCAAATTCTTACA[C/T]AGTAACAGAAAAAAT	54476
rs554904165	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5698789	AATCTTGTGCAGAGA[A/G]ACTACACAGGAAACC	54476
rs554906916	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5752006	GCCTGGCCAAGATAG[A/T]TAAACCTATCTCTGC	54476
rs554908921	snp	A/C	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5644744	TCCTGGGCTTAAGCT[A/C]TCTGCCCGACCTTGG	54476
rs554924316	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671032	TGTTGCTAATATCAT[C/T]TGTTATAGCAACAAA	54476
rs554932910	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5744186	AAGAAGAATCGAACG[C/T]AAATTCCAGAATGGA	54476
rs554937380	in-del	-/TC			intron-variant	RNF216	GRCh38.p7	7:5633405	CACGGTGAAACCCCG[-/TC]TCTCTACTAAAATAC	54476
rs554954358	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5698203	GTTTGGGCTAGAGGG[A/G]CACTCAAAAGGTCAT	54476
rs554969178	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5658676	AAAAAAAAAAAAAAA[A/T]TTTTTTAACTGACTT	54476
rs554974964	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5729277	TTCATTTAGTCCGTC[A/G]CGATGAGCAAATACC	54476
rs554979321	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5734039	AAACCCAAAAAGAAA[C/G]TATTTTAAAAGCTTA	54476
rs554993772	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5704236	TACGTTTATATTAAT[C/G]CCGTATTAATATAAA	54476
rs555014980	snp	G/T	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5757955	AGCCCAGCAGTTCAA[G/T]ACCAGCCTTGCCAGG	54476
rs555016851	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5687265	ACTGGGCATGGTGGC[A/G]GGCGCCTGTAATCTC	54476
rs555024685	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5723696	TCTACAAACTTCCCT[C/G]TAATGTATTTTCCTG	54476
rs555029179	snp	A/G/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5660249	TGAGCCACAGAGCCC[A/G/T]GCCCTGTTTTAAATT	54476
rs555033105	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5724409	ATAGCACTTTCTCCA[A/C]CACTGAAGTCAGAAA	54476
rs555037991	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5747847	ATAGTGGCACAATCA[C/T]AGCTCACTACAGCCT	54476
rs555040977	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781123	CCCGCCTGGGCTGGG[A/G]TTCACAGGCACGGCC	54476
rs555061680	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675200	TAACAGTCTGTTGTA[A/C/T]GCTAGTTACTATGCT	54476
rs555066746	snp	C/T	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5719969	AGATGTTTCCAACGG[C/T]CAAAACTTGGTAAAG	54476
rs555085322	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5655142	CCATTTTTGAGATGA[A/G]GCACAGGCCCACCAG	54476
rs555115026	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5686466	CACAGTGGTGGCTTA[A/G]GAGTCTGAATGTTAT	54476
rs555127244	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680789	GGGCTCCCCTGTATC[C/T]CTGAAGGACACAGCC	54476
rs555146877	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5655519	GCTGAGGCAGGAGAA[C/T]TGCTTGAACCTGGGG	54476
rs555153157	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5714500	TGACCTCAGGTGATC[C/T]GCCTACCTCGGCCTC	54476
rs555160805	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5737317	TTAAACACATGCTTG[A/C]AGGCAGCATGCTTGT	54476
rs555174473	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5728537	CGAGATTAGGCCACT[A/G]CACTCCAGCCTGGGC	54476
rs555197380	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5628798	AAAATGTTGGGATTA[C/T]AGGCATGAGCCATCA	54476
rs555213336	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5644185	CTTGTTTTCACTTAT[A/G]TTGGGTGAGTACCTG	54476
rs555221462	snp	C/T	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5761385	CTTGATACAAATATG[C/T]TAACAAAGAAATGGG	54476
rs555222351	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5639265	CCTTTTCAGACAATG[A/G]CCTCATGTGATCCTT	54476
rs555243626	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663649	TTCGTGCCTGTAATC[A/G]CAGCACTTTGGGAGG	54476
rs555258014	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5627540	ACCACGAGGTCAGGA[A/G]ATAGAGATCATCCTG	54476
rs555261119	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5634088	TAACCATTTGAGCGC[C/T]TGGCACAAAACTATT	54476
rs555294497	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663140	GCACTTAGCTTATGC[A/G]TTGTTACTGCACTTT	54476
rs555295636	in-del	-/T	0.0193772	0.0965046	intron-variant	RNF216	GRCh38.p7	7:5628457	AATACAACTTAAAAG[-/T]TTTTTTTTCTTTTTT	54476
rs555296906	snp	A/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712918	CCATTTATAGAAAAA[A/T]AAAAAGCGTCAGTGG	54476
rs555325435	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5637286	ACCCAGCAAAAGAAG[A/G]ATGACTCGGGCTTGG	54476
rs555326240	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5686255	AAAAAAAAATGGAGC[A/G]TGCTTCTCCAAACTC	54476
rs555331261	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664701	CAAGGGTAGGCTGCA[C/T]GCTTCCCCCACTGGC	54476
rs555351482	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5762195	TTATGTAAGTTAATA[C/T]AAAAATTTAAAATAC	54476
rs555361502	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5718783	AACTCCTGATCTCAG[A/G]TGATCTGCCCACCTC	54476
rs555381605	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5691700	CATGGACACATGGTT[C/T]TGGCCACCCGGCAGG	54476
rs555395018	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5736533	TTTCAGCCTCTGCCC[A/G]GCCGCCACCCCGTCT	54476
rs555399370	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5632758	TTCCAGCCTGGGCGA[C/G]AAGAGCAAAACTCCA	54476
rs555405794	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5781752	ACTGCGGAGGAGGGA[C/T]CGGGGGGCTCACCAT	54476
rs555425275	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5728666	TTGGCTTGGTTCTTC[C/T]CTTCCTACAGGTAAG	54476
rs555452126	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5732170	TTTCCTATAAAACCA[C/T]TGTCATCAGTGGTAA	54476
rs555457938	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643069	ATGAAATAATAATGG[G/T]TATGGAGGGAGAAAA	54476
rs555512558	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782112	ATCCCAGCACTTTGG[A/G]AGGCCAAGGCGGGTG	54476
rs555531536	snp	C/T	3.29451e-05	0.00405851	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741479	TACCTTCTTCCAAGA[C/T]GATGACTTTCTGCTC	54476
rs555536253	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5627530	AGGCAGGCGGACCAC[A/G]AGGTCAGGAGATAGA	54476
rs555553028	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5766184	AGTTTTAGCTACCCA[C/G]GAGTCTGAAGCAGGA	54476
rs555577083	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5761884	CATTGCTGGTTTGAA[A/G]AGTAACTTGGAAAAG	54476
rs555588544	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669173	GCCTGAGAGGAATAT[G/T]GGCGGTCGGGCTCCA	54476
rs555611174	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5708186	GGAAAATGTTCCATG[A/C/T]GCAACAGAGGAGAAA	54476
rs555611708	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5756900	TTTGGCCTTCCAAAG[C/T]GCTGGCATTACAAGC	54476
rs555622020	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5728054	CTTCTCAGCACATTG[G/T]CAACCAACGTTTCCC	54476
rs555623873	in-del	-/A	0.0103295	0.0711199	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664858	GGAGTGCAATGGCAC[-/A]AATCTTGGCTCACCG	54476
rs555649928	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5647271	AAGAACTAAAGTTTG[C/G]TGAACAATGCAGCTG	54476
rs555671485	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5691176	ATCAACGTGACAGCA[C/T]TTCTGCTCATGCCAA	54476
rs555678437	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5717832	TTGTCGCCCAGGCTG[C/G]AGTGCAGTGGTGCAA	54476
rs555683716	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5723414	GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC	54476
rs555721840	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5708145	ATTTGTTAAGACCTG[A/T]ATTATGATCTAATAT	54476
rs555725003	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5735540	AAAACCAGTAACACG[A/G]TAGATGAGTTAAAAG	54476
rs555731842	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5700457	TCTCTCCCTTGATGA[A/G]GCCACAGACACAGAA	54476
rs555743883	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5694712	ATGCCCTTCAGCCTA[C/T]GGAAAGTACATTCTC	54476
rs555745151	snp	A/G/T	0.000115696	0.00760505	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741033	AGCTTCTTGCCCCCA[A/G/T]ATGTTTTCCAAATTG	54476
rs555788637	snp	C/G			upstream-variant-2KB	RNF216	GRCh38.p7	7:5783608	TTCTCTAAGACAGTA[C/G]AGTGTGGCTTATGGG	54476
rs555805460	snp	A/G	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5695172	CTTCATCTGTACAAC[A/G]AGCATGTCTGGGTTA	54476
rs555813068	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5740581	TATTTAACTGTAAGA[C/T]ATTTAAATGTAAACA	54476
rs555813834	snp	C/T	0	0	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621400	AACTCATCCGCCCGC[C/T]TCGGCCTCCCAAAGT	54476
rs555834431	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674152	CTCCTGCCTCAGCCT[C/T]CTGAATAGCTGGGAT	54476
rs555834567	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5771070	CTTGGCCTCCCAAAG[C/T]GCTGGGATTACAGGC	54476
rs555837364	snp	G/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5764808	GCAGTGGCTCATGCC[G/T]ATAATCCCACCACTT	54476
rs555844197	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5660343	TGTCACCAGGCTAGA[G/T]TGCAGTGGCGCAATC	54476
rs555846606	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5773513	CCCAAAGTGCTGAGA[C/T]TACAGGAGTGAGCCA	54476
rs555848298	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621755	CCTCTCATCTGTCAA[C/T]GGGCCAGAGTGATGC	54476
rs555860280	snp	G/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5701879	CCCAGCAAAAGACGT[G/T]TCCCAAACAATGCCT	54476
rs555864199	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5646347	CCACTGCACTCCAGA[C/T]GGGGTGACAAGGCGA	54476
rs555933810	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5647928	TAAAGCTACTTGCCC[C/T]GTAGCCACCAAAATC	54476
rs555938261	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5773812	ACTTCAGTGATCTGC[C/G]TGCCTCAGCCTCCCA	54476
rs555953028	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5652823	GTTGGGGGAGGAGAG[A/G]GGAGTGGTAAGAATC	54476
rs555955579	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5626781	CCTGAGTATCCCTGC[A/G]TCCAGGAAGCTCATC	54476
rs555967021	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5769480	GTAATCCCAGCACTT[A/T]GGGAGTCTGAGGTGG	54476
rs555974554	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5685025	GGGGTGAAGAGAGTG[C/T]CCAGGATTCTTGCTG	54476
rs555975296	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678338	CAATATATTACCTGC[A/G]TTTCATAAACAGGAT	54476
rs555984713	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5715798	CCGAACTGGAGTGCA[A/G]TGGCACGATCTTGGC	54476
rs555997854	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5750851	ATAACCTGCACTCCC[C/T]GCTTTAATTTAACCC	54476
rs556020989	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5655247	CTACGTCACAGTGCT[G/T]CTTCTGTAGGTGAAC	54476
rs556033439	snp	A/G	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5721994	GTGGCACATTCACAG[A/G]TCACTGCAGCCTCAA	54476
rs556035692	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780484	GAGGGATCACCTGAG[A/G]TCAGACGTTAGAGAC	54476
rs556039605	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5711259	CAGCTCTGCTCCCAC[A/G]TAATATAGTCAGTTC	54476
rs556046206	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5734226	TATCAAAAGTAGATG[C/G]AAAATTTCATTGCTA	54476
rs556054250	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5770154	AAGTTTAAGGCCAGC[A/G]AAACCCCATCAAACA	54476
rs556062764	in-del	-/AAAAAAAAAAA	0.251296	0.249997	intron-variant	RNF216	GRCh38.p7	7:5687395	GTGAAACTCCACCTC[-/AAAAAAAAAAA]AAAAAAAAAGAAAAA	54476
rs556063726	snp	A/G	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5748986	TACCAAAATATATGA[A/G]AGAACTCTGATAATC	54476
rs556091503	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5687124	AGGAAGACCAGGTAC[A/G]GTGGCTCATGCCTGT	54476
rs556091613	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5742384	ACTACTAAAACAAAA[A/C]TAACTCCACAGCAGA	54476
rs556095688	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216, RNF216-IT1	GRCh38.p7	7:5662118	CGTGCAGCTGCAGCT[C/G]TGCAGGATGTCTGCT	54476
rs556102933	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5706173	TGCAGTGAGCTGAGA[C/T]TGCACCACTGCACTC	54476
rs556105588	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754269	CAAGCAATCCTCCCA[C/T]GTCAGCTTCCCAAGT	54476
rs556111615	snp	A/G			utr-variant-5-prime, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781570	GCCGGCTAGCCAGGC[A/G]GGTTCGGCGGCCTTC	54476
rs556118282	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5631790	AGAGATCAATCCTGG[A/G]AACATTCTGATATCT	54476
rs556120630	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679601	ATGTGCAATTATTTG[A/G]TAAGGCTTAGCTCCA	54476
rs556120697	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673439	AGAAGAGAAGAAGGG[A/G]CCAGACTAACAAGAG	54476
rs556121108	snp	A/T	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672091	GGCAGTGGATCAGAG[A/T]AGTTCCCGCCCCTTT	54476
rs556141768	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5631285	AGCCCACTTGTCGGC[C/G]TCTGGTCCCTGGCAC	54476
rs556142402	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754492	TTTAAGGATGAGGAG[C/T]TGCCAAGCTCCTCAC	54476
rs556161233	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5626276	TCAACATGAAGGACT[A/G]CAGTAACTCAAGAGG	54476
rs556169919	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5731164	AAGCAGCTACTCTTT[C/G]TCGAGAAAACTATGA	54476
rs556180564	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666998	TTTTTGTACAGACCA[C/G]GTCTTGCTATGTTGC	54476
rs556185373	snp	A/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5682891	AAAGCTTTACATATA[A/T]AGCTTTGCATTGCGT	54476
rs556201337	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677253	ATCAGCCAAGGAGTC[A/G]CTATCTGCTGTTGTC	54476
rs556204009	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5760561	TGTAGAACAAAAAAA[C/T]ACATGTTCCAAAATT	54476
rs556224536	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5726755	TCCCAGCTACTTGGG[A/G]GGCTAAGGCATGAGA	54476
rs556228200	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5749970	CTTTTAAGGTTATTA[C/T]AGCTTATAGCAATTT	54476
rs556270310	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5688498	AATACAGAAGTTATT[A/G]TAAACAAAAAGCAAA	54476
rs556277383	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656948	AGACCTTTGGGTCTG[C/T]TGGCAAAGAATCCAA	54476
rs556281643	snp	G/T	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5731536	CAGACCCAACACATG[G/T]TAACTATCCAGGCTC	54476
rs556283910	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5778475	TTATTTAGGAAACTA[C/T]GTGTAATTTTGGTCT	54476
rs556285163	in-del	-/GAA	0.0146672	0.084371	intron-variant	RNF216	GRCh38.p7	7:5647118	GAAGTTGTGAAAGGT[-/GAA]GAAAAAAAAAAAGGG	54476
rs556290822	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5646301	TTGGGCCCAGAGGTG[A/G]AGGTTGCAGTGAGCT	54476
rs556321142	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5779265	TTTATCAGATTTCTC[C/T]ACAGGGGCTTCAGGA	54476
rs556397627	in-del	-/AA			intron-variant	RNF216	GRCh38.p7	7:5654687	GCCAGACTCCGCCTC[-/AA]AAAAAAAAAAAAAAA	54476
rs556414151	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5641800	AGAACTTTGAGAGGC[C/T]AAAGCAGGAAGATCA	54476
rs556418691	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5660864	TGTGAGCCACCATGC[C/G]TGGCCTGGGGAACAT	54476
rs556430146	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667491	GCTGATAAGGAACAA[C/T]GCCCGGGAACCAGGG	54476
rs556448775	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5735399	ACTTAACATATCAGA[A/G]CAATCAAACTCACAG	54476
rs556451776	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5706531	CAATGTCCCTCAAGG[C/T]GGTTTATCTGTGTTG	54476
rs556454912	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5636645	TGCTGGGTTGGAATT[C/T]GATCGGTCTCCTGGT	54476
rs556483049	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5655959	CCTCCTGGGCTCAAG[C/T]GATCTCCCACCTCAG	54476
rs556486613	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5725718	AGCCGGGCATGGTGG[C/T]GCACGCCTGTAATCC	54476
rs556505251	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5783497	TGCTGCACTCCAGCC[C/T]GGATGACAGAACAAC	54476
rs556506074	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5661699	TCCCAGCTACTTGGG[A/G]GGCTGAGGCATGAGA	54476
rs556521805	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5639402	GAGAAACACACTTCT[A/G]TTTTCCTTTTTTTTT	54476
rs556534865	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5735691	GTTACAGAAGACAGG[A/C]AACAGCTACAAAATT	54476
rs556537851	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5651602	TAAGGCTAGATTGTT[A/C]TGAGAGAAGAGAAAG	54476
rs556543538	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5693416	ACCTCCACTGTACTG[A/G]GGTACCAAAATGTAC	54476
rs556559838	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5758951	TTTGGATCTGTGTCC[C/T]TGCCCAAATTTCATA	54476
rs556562678	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5639847	TCACTGCAAGCTCTG[A/C]CTCCTGGGTTCACGC	54476
rs556589351	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5689640	TTGAGTAAAATCATT[C/T]AGATATGCAGAGTTT	54476
rs556612648	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5639739	TGCTAGGATTATAGG[C/T]ATGTGACACCGTGCC	54476
rs556664279	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5646678	AGCCTGGCGACAGAG[C/T]GAGACTCCATCTTAA	54476
rs556670871	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5721551	GAATGTATGTCCGCA[A/G]TTTACCTGCGAATTG	54476
rs556672502	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5763469	AACCCATTTCTACTA[A/G]AAATATAAAAATTAG	54476
rs556672919	snp	A/C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5715854	TCAAGCGATTCTCCT[A/C/G]CTTCAGCCTCCCGAG	54476
rs556679534	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5777778	AGTTTAACAGCTCTA[A/G]GAATCCTATTATCTG	54476
rs556684912	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666228	AAGGACTATGGGTCC[C/T]GCTCTGCAGTGGGGA	54476
rs556688221	in-del	-/A	0.388775	0.207946	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663587	AGACTCCACCTCAGG[-/A]AAAAAAAAAAAAAAA	54476
rs556693918	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5743532	TGGGAAGCTTCACTA[A/C]GAAATGCCATTAAGT	54476
rs556696064	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5710195	TGAAACCTCATCTCT[A/T]CTAAAAATATAAAAA	54476
rs556705378	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5705528	TGGAACAAACTCAAA[C/T]CTCAGTAGTTCAAAA	54476
rs556719773	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5693075	CTCCATATTTGCACA[A/C]CGGGATTCCACGTCA	54476
rs556738639	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5640494	TCCACCTGCAAACCT[C/T]ACCTGCTTTCTTTCC	54476
rs556742229	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5729877	ATATTTACGAACAAC[G/T]ATTTTTTTTCTATTA	54476
rs556743125	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5634671	CACCCAAATACCACT[A/G]TCTGGAGCACTTCCC	54476
rs556782429	snp	A/G	0.000798403	0.0199641	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619714	GGCTTCTCCTGGTTT[A/G]CTTGACCTTTAGGTG	54476
rs556783995	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665798	TGTTTCTCTCGAATG[A/G]CTGTTTAACAGAATC	54476
rs556805605	snp	G/T			upstream-variant-2KB	RNF216	GRCh38.p7	7:5783393	CCTCGGCCTACCAAA[G/T]TGCTGGAATTACAGG	54476
rs556825349	in-del	-/AAGAA			intron-variant	RNF216	GRCh38.p7	7:5774056	GCCCCAACCTGTGAG[-/AAGAA]AAGAATTCTGATGAT	54476
rs556831267	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5655105	TATTAATTCATGGGT[C/T]TTCCTCATAAGGGAA	54476
rs556853618	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5692442	GGGAAAAGGCAGCAG[C/T]TGGAAACAGTCTTGA	54476
rs556865455	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5625147	TCACAAGCAGCAGAG[C/T]GGCAACACCGTGGCA	54476
rs556872689	snp	G/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5709761	TTTTATTTTTTAAAT[G/T]TTTTTCTTTTAAAGA	54476
rs556874714	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5720550	AGCTGCACAGGGGGA[A/G]GCACTCCTAACTTTC	54476
rs556886210	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5650211	GAAGCCCAACATTTG[A/G]GAGGCTGTTTTTGAT	54476
rs556926898	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5687232	GAAACCCCATCTCTA[C/T]TAAAAATACAAAAAT	54476
rs556933395	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5770856	TCTGTCGCCCAGGCC[A/G]GAGTGCAGTGGTGTG	54476
rs556937664	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5697192	AGTTCTCCCCATCTC[C/T]GCCAATAAGACCCCA	54476
rs556951415	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5650998	CTACAGGCTACATAC[A/G]GTGCTTGCCTTGCCC	54476
rs556998954	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5697537	CATGGCTGGGCTAAG[C/G]CTTTTTTATTCTTTT	54476
rs557023972	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676408	CCTTAAAAGTGCTGA[C/T]GGCAGTTGCAAAAAG	54476
rs557030210	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5772683	ATAGAATGTGAAGTT[A/G]TAGATACTATCAAAA	54476
rs557041830	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5769317	GAGAAGGGGTTTCAC[C/T]ATGTTGGCCAGGATG	54476
rs557044294	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5623905	GCCTGAGATGTGGCC[A/G]CGTGGGTGAAGTCAG	54476
rs557075797	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5633659	TTGTTTCCTTTCCTT[C/G]AATTCCTTTGAGCTC	54476
rs557110332	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5628557	AGACAGTGTCTTGCT[C/G/T]TGCTGTCCAGGCTGG	54476
rs557176754	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753735	GGAGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA	54476
rs557194874	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782392	CCTGGCCTCAGGAAG[A/T]TTAGGTTTTAGTGAG	54476
rs557250051	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5742827	TCTTGAACTCCTGAC[C/G]TCAGATGACTGGCCC	54476
rs557252413	snp	A/C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5771962	CAAGGGGCCGGGCGT[A/C/G]GTGGCTCACGCCTGT	54476
rs557260369	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5714555	GAGCCACCCGGGCAA[A/G]AAGTCATCTTCTTAA	54476
rs557288585	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5714006	AAAACATAAACTTTA[C/T]TTATTTATTTTTCTG	54476
rs557289147	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5761844	AAAAAAGGCAAGTAT[G/T]TAAGACATGGGAAAT	54476
rs557316346	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675774	TAACGCAATGGTGCG[A/G]TCTCAGCTCACTGAA	54476
rs557369287	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5685631	GAGGGGGCATAGTGG[A/G]AAAGGAAGTAAAACA	54476
rs557383240	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5686165	AAGGCAGAGGTTGCA[C/G]TGAGCCGAGATCATG	54476
rs557383340	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679872	CGCCTTTCTGCTAAG[C/T]GGCCAGAGTCCCTGG	54476
rs557410663	in-del	-/AG	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5628069	CCCAGCCTGCCATTC[-/AG]AGTTCTTCCTGGAGA	54476
rs557445466	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5680336	TGCGATCCACTCCCC[C/G]AAGCCCAAGTCTCCT	54476
rs557446811	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5698243	CTTCTGGTTGCAGCT[A/G]GACTGCATGTAAGCA	54476
rs557470793	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5654547	CAAAAATTAGTTGGG[C/T]GTGGTAGCTGGTGAC	54476
rs557484475	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5653974	AAGGGCATGATGAGC[A/C]GTTTTTTCTTTATCC	54476
rs557506981	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5691112	TTTTAAGTTCCGACA[A/G]AAGCACACCCATTTC	54476
rs557558250	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674790	CACCTGAGATCAGGA[C/G]TTCAAGACCAGCCTG	54476
rs557573213	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643682	TTTGCTGTGGTAAAA[G/T]GCACATAAAATTGAC	54476
rs557593140	snp	C/T	0.00557542	0.0525036	intron-variant	RNF216	GRCh38.p7	7:5633221	TGACCTTGTGATCCA[C/T]CCGCCTTGGCCTCCC	54476
rs557610232	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5657480	GCTGAGGCAGGAGAA[C/T]AGCTTGAACCCAGGA	54476
rs557610507	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663162	CTGCACTTTTAGTGG[C/T]GTCTTGTAATTATCT	54476
rs557612061	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5638242	AAGTGTAGATATATA[C/T]AGAATTACTTTTTGT	54476
rs557615022	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5649205	TGGCCAACCACGGCC[A/G]ACAAAGTAAAACCCC	54476
rs557623321	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5765375	AGGCTGAGGTAAGAG[A/G]ATTGCTTCAGCTTGG	54476
rs557640569	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5697607	CTGGCCTCAGCCTCC[C/T]GTGCAGCTGGGACTA	54476
rs557650537	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5638780	GTAGCTATGACTACA[A/G]GTGAGCACCACATCT	54476
rs557651117	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5761284	CAAAAAAAAAAAAAA[A/C]CACACAAACTCAAAA	54476
rs557683610	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5742140	CAACCTCTGCCTCCC[A/G]GGCTCAAGCAACTCT	54476
rs557688941	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5653522	AGGAGAAAGGCGTGA[A/T]CCCGGGAGGCGGAGC	54476
rs557691351	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663847	AGGGTGCAATGAGCC[A/G]AGATCCTGCCACTGT	54476
rs557694869	snp	C/T	0.00795532	0.062565	intron-variant	RNF216	GRCh38.p7	7:5731841	CTGGCAGAAAGAGGG[C/T]AGAGAAAAAGTGCTC	54476
rs557701619	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5695024	AACTTTAACTGAGCC[-/A]AAAAAATACACTAAT	54476
rs557711358	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5690771	GCAATACAGCCCACA[C/T]TAGAGCTCATGCCCC	54476
rs557716671	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5647834	TACTACAAACCTATA[A/T]TGGAGCCCTATGATA	54476
rs557718479	snp	C/G	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5641996	TGAGACCGTGTCACT[C/G]CACCCCAGCCTATGT	54476
rs557733510	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5734010	AAAAATGTAGTTATT[A/G]TCATGCCACTTAGAA	54476
rs557743867	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5648836	TTCTACAGGCCAATT[A/G]TCAAATGCAATGAAT	54476
rs557754686	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5723009	AGAATAGAAAAGCAC[A/G]TGGTTAGACAGTAAG	54476
rs557817359	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5751969	GAGGGGGGCGGATCA[C/T]GAGGTCAGGAGTTCA	54476
rs557826712	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5726641	GGCAGGTGGATCACC[A/T]GAGGTCAGGTGTTCA	54476
rs557830055	snp	C/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753099	ACTAGTGTAACGTAC[C/T]TCCTCAAGCAGCCCG	54476
rs557841681	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781036	GCGGCGCCCTCGCGA[C/G]TGCCGGGTGACAGTC	54476
rs557842076	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5745575	CACTACAGATAATAA[C/T]GGTAAGGTGATTGAG	54476
rs557865347	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5723371	TAAATGCAATTGGCC[A/G]GGTGCGGTGGCTCAA	54476
rs557865596	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736174	TGATGCCCAGCCGAA[C/G]CTGGACTGTACTGCT	54476
rs557865990	snp	A/G	5.33367e-05	0.00516386	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5740974	AAAATAAAACTTACC[A/G]TTTCTTTCACTAGTA	54476
rs557867332	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5718050	TCCATAAAATAAGGA[A/G]AGGTAAACCAAAGAC	54476
rs557889349	snp	G/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5636804	TTTTGAGCAAATCTA[G/T]AAACTTTCTCAGGTT	54476
rs557890890	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5771048	CTTGACCTTGTGATT[C/T]GCCCACCTTGGCCTC	54476
rs557896612	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5726353	CTGGTGAGTCCCATT[C/G]TGTAGGCAAATCTTC	54476
rs557897349	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5770642	AGATGACTTTAGAAT[C/T]TACAGGAAAACAGCC	54476
rs557923047	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5626225	GAACACTCCACAAGG[A/G]GGAACTTACTACCTT	54476
rs557932767	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643237	TTTGCTTCTGCATTT[G/T]TAAGAGTAGTACTGG	54476
rs557973440	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5701255	AATCTACCCCTTTAC[A/G]TGGCAGAACACTGGG	54476
rs557973736	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5707581	GTGAACTTGCACGGA[C/T]ATAGATGCTTTTGCT	54476
rs557975236	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5765642	CTGAAACAAACAAAA[A/G]GCATGAAAAAGAAAC	54476
rs557990336	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5770753	AATTAAGACAATATT[A/G]TATTGACAAAAGAAA	54476
rs558007477	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5721967	TTGCTCTGCTGCTCA[C/T]GCTGGAGTGCAGTGG	54476
rs558017321	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5626999	ACTAATCACAACCAA[C/G]AGGACTGCACAACCA	54476
rs558020386	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5651690	AGTCTCGCTCTGTTG[C/G]CAGGCTGGAGTGCAC	54476
rs558022889	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5732079	GTCCACGGAACACAA[C/T]GCCTGAGGCCCAAAG	54476
rs558036921	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5727457	CATTTAATAACATAG[C/G]CTGGGCATGGTGGCA	54476
rs558050955	snp	A/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5772129	TCCCAGCTACTCAGG[A/T]CGCTGAGGCAGGAGA	54476
rs558055762	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621957	GGCACACACGGGGCA[C/G]GGGTGGCACCCAGGG	54476
rs558055875	snp	A/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5627476	AAAGACTAGACACTC[A/G]GTGGTTCACGCCTGT	54476
rs558070664	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5624836	AACTCAGGGGCCACA[C/T]TGGGCAAGCCCCAGA	54476
rs558070957	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5722516	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	54476
rs558079013	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5647191	CTGGTGGGAGATAGG[A/T]GTTTTTGGAATTCCC	54476
rs558107710	snp	C/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5630763	TGAGAGATTACTATG[C/T]ACCAGCCCCTGTCTA	54476
rs558142012	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5699951	TACCACATTGCAACT[A/G]GAATCTGACCTTGAA	54476
rs558144464	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5631174	ACAAACAGCCAAAAC[A/G]CAGAGCAAGGGGCTG	54476
rs558145274	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5746143	CTCATGGAGCTGCAA[A/G]TGTCGGAAGTCCTTC	54476
rs558152050	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5771861	ATTAACAACGGCTGA[A/G]TACCCCGAGGAAACG	54476
rs558153187	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5750435	TCTTACTGTGATTAT[A/C]TTTGGTAGAAATGGG	54476
rs558185114	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5625583	TTATTAATGTCACAG[A/C]CAAGACAGAAATGAG	54476
rs558192366	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5637175	CAGGGGGCTGAGGAG[A/G]TGAGTCAGCAGAAGG	54476
rs558195551	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5653356	AGGAATTTGGGAGGC[C/T]GAGGTGGGCGGATCA	54476
rs558205508	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5700375	GGAGGTAAAACATTT[A/C]TTATAAAAAGGTATT	54476
rs558215493	snp	A/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5775028	TGAGATTACAGTCGT[A/T]AGTCACTGTGCCTGG	54476
rs558220990	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673333	GCTGTTCAAGAACAG[A/G]CTCGACAGAATGGAG	54476
rs558237455	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668297	GGCGCAATCTTGGCT[A/C]ACTGCAAGCTCCGCC	54476
rs558257533	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664148	TCTTCTCCATGCAGA[C/G]AGTTGTTTTTTTGTA	54476
rs558263166	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5769423	GCCTGGCCGCAAATG[C/T]CTTATTTTAAACAAA	54476
rs558303167	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5775626	TGTAATCCCAAAACT[C/T]TGAGAGGCCGAGGTG	54476
rs558309612	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5707031	CCATTAATCAGAGAC[A/T]ACCTTTTCCCCCGGT	54476
rs558323779	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5624015	AAGCCTGCATGGCCT[A/G]GCTGCTGCTCTGTCC	54476
rs558323801	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5661568	AGCATTTTGGGAGGC[C/T]GAGTAGGGTGGATCA	54476
rs558343199	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5694174	AGGTCTTACTAAAAA[A/G]GGCATTTTGTAAACT	54476
rs558343206	in-del	-/AT			intron-variant	RNF216	GRCh38.p7	7:5742454	AAATGTTCAAAAAAC[-/AT]ATAAAAAAATCTAAA	54476
rs558368715	snp	A/G	0.0154538	0.0865337	intron-variant	RNF216	GRCh38.p7	7:5732192	CAGTGGTAATTCTCC[A/G]TCCTAGAATTCACTG	54476
rs558398385	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5778809	AGTGCAGTGGCACAA[C/T]CTCGGATCACTGCAA	54476
rs558398469	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5773197	AAGAACAGCTCTGGT[A/G]TCAAATTTGAACTGC	54476
rs558420412	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5715784	TCTCACTCTGTTGCC[C/T]GAACTGGAGTGCAGT	54476
rs558434916	snp	C/G	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5755159	GGAAAGAAGGAAGGA[C/G]AAAGGAAGGAAAGAG	54476
rs558442181	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5749344	TTAGTAGAGACGAGG[C/T]TTCACCATGTTGGCC	54476
rs558453410	in-del	-/C	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753822	GAACACGGTGAAACA[-/C]CGTCTCTACTAAAAA	54476
rs558458125	snp	A/C	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5705637	GCGGTAGGCTGGGCA[A/C]GGTGGCTCACCCTGT	54476
rs558480829	snp	A/G	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5758601	GATGTGGAGTCAAAG[A/G]AGGTTATTTTGGACC	54476
rs558481290	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5763732	GCACCACCATGCCTA[A/G]CTGAATTTTTAAAAT	54476
rs558500497	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678467	TTCAGAGATTCATGC[C/T]ACCTGGCGTCCCCAC	54476
rs558502679	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5684927	GGTGGGGTGGGGTGT[C/T]AGTCTGTAGCTTTGT	54476
rs558553071	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5777143	CGGCCTTCCAGCAGT[C/T]TTTGACAAGGCATGT	54476
rs558572645	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5758875	GTTGGGAAGACGCAA[C/T]TGTATTTAGCAATGT	54476
rs558580497	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682260	CTATCTTGTTCTGAA[A/G]TCCTTTGGAATCACC	54476
rs558581036	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5735676	GATTGTGGGAGAAGA[A/G]TTACAGAAGACAGGA	54476
rs558619284	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5635414	TTACTCTTTTGTAGA[A/G]TAAATTTTTAAGGTT	54476
rs558623356	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5731145	AACTGGAAAATTTTA[A/G]GAAAAGCAGCTACTC	54476
rs558640972	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5682653	CTCAAATGATCCACC[C/T]ACCTCAGCCTCCCAA	54476
rs558649042	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5723663	AAAAAAAAAAATAAA[C/T]AAATAAATGCAATTA	54476
rs558707713	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5759419	AAGACCTTTAGAATG[C/G]TCCACTTCCACTTAA	54476
rs558710798	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620125	CACAGTAGTTGAAAC[A/G]GAATTATTTTATCTA	54476
rs558724613	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5749920	ACTGCTGGTTCTTTT[A/C]ATGTTTTGTTTTCCA	54476
rs558727347	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713484	TCCAGACCTTTCCTC[C/T]CCCTCAGTTTCAGAA	54476
rs558743826	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5702045	AGGGATCAGGGAGGT[C/T]GGCGACATCTGAGGC	54476
rs558792452	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5744324	AGCCAGGTCAGAATA[A/G]CCATAGTAAGGCATA	54476
rs558802732	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665633	ACCACACATAGCTGC[C/T]GGCTTTTTACTATAC	54476
rs558822123	snp	G/T	0.00302641	0.038782	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741572	TTTCTGTTTGGCCAC[G/T]TGGCTTAGTGAATTC	54476
rs558844440	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5763395	CAGCACTTTGAGAGG[C/G]TGAGGAGGGCAGATC	54476
rs558862534	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5634197	GCTGGCCAGCCTCCT[C/G]TGACCATGGGGGAAG	54476
rs558880180	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5730174	GCATGCTGAAGTACT[C/T]AGAGGGAAGTGTACT	54476
rs558885879	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5744831	TACAAAATTAGCTGG[G/T]AGTGGTAGCGCATGC	54476
rs558887585	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5739086	AGTGAGTGTTTAATG[C/T]GGACAGAGTTTCAGT	54476
rs558891835	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666485	GGAGCAGGGTGGGCA[A/G]AGCTGTAAGGTGGAG	54476
rs558919396	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768401	CACACACAGCTTAAA[C/T]TGACAGACCTTAAGG	54476
rs558924409	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5655889	TGAGCCAGGGTCTCA[A/C]TCTGTCACCCTGGCT	54476
rs558925667	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739415	TTCAAATGGCAATAC[A/G]AGACAGATGGCAAAA	54476
rs558959108	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5698378	GAGCTGTCTTAGATT[A/C]TTTTATACACACACA	54476
rs558960438	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5725032	CCTTTGAGACCAGTT[A/T]TTCCCCCCAAGCTTA	54476
rs558976871	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620480	GTCCAGGCAGGAGCC[C/T]GAGGTTCAGGCCCTG	54476
rs558988997	snp	A/C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5720681	ACACTTTGAGAGCCA[A/C/T]TGGTTTAGAAGATAC	54476
rs559012423	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670026	CTGCCTCCCAAGTTC[A/G]AGCAATTCTCCTGTC	54476
rs559024068	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664683	GGAAGGCCAGTTGCC[A/G]CCCAAGGGTAGGCTG	54476
rs559027239	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5660365	GGCGCAATCTCGGCT[C/T]ACTGCAAGCTCTGCC	54476
rs559116698	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5697744	GCAAGGGTGCTCGCC[C/T]GGAGAAGACAGAAGC	54476
rs559120658	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5634624	GCTGGCCCTGGCTTC[C/T]GCAGCCACCTCCTCA	54476
rs559151584	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5772004	TTTGGAAGGCCGAGG[C/T]GGGTGGATCACCTGA	54476
rs559172743	snp	G/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5746916	AGATTCTTACTGGCA[G/T]TCAGAAGCCTCAAAG	54476
rs559194242	snp	G/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5710087	TCTTCAGGCTGGGGG[G/T]GGTGGCTTACACCTG	54476
rs559203768	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5747412	TTTCCTGAGGATGAT[A/G]TTCAGGACCTGACAA	54476
rs559206745	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5704794	CCAGGCCGTCACTGC[C/G]TCAGGTCCCCATATA	54476
rs559209772	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5649362	CTCTAACCTAGGTGA[C/G]AGACGGAGACTCCGT	54476
rs559212682	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5629603	GGAGGCCGAGGCGGG[C/T]GGATCACGACGTCAG	54476
rs559244544	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5756991	TTTTCCTCAAAACAT[C/G]GCATTACATGTATCT	54476
rs559249722	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5629964	GAGTCCATTCTGGAG[C/T]CAAGTCCCTCAGGAA	54476
rs559249805	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5624178	TCATGCAGTGCTGAG[A/G]CCCCGTGGGACAGTG	54476
rs559298179	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5729822	AAAGAAGTATAGTTG[C/G]GGATTTAAACCAATC	54476
rs559301907	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5627196	ATGTTACGGCTAGTT[A/G]GCGGTAAACTGGGAC	54476
rs559317146	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5772476	CAGTGGTGCGATCTC[A/G/T]GCTTACTGCAACTTC	54476
rs559318731	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5657139	CTCCCTTACTTTTAA[A/G]TGGTTCCTACAGTGA	54476
rs559334040	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5752117	TTGAAACCAGAAGGC[A/G]GAGGTTGCAGTGAGC	54476
rs559340043	snp	C/T	0	0	intron-variant	RNF216	GRCh38.p7	7:5627619	GAGCGTGGTGGTACA[C/T]GCCTATAATCCCAGC	54476
rs559340410	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680504	CCTCCCGGGTTCAAG[C/G]GATTCCCCTGCTTCA	54476
rs559352348	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5727122	GGCAGCAATGAGAAG[C/T]GGGGTGGCTATGATG	54476
rs559369102	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5759145	TCTTGTTCCTGCTCC[A/G]GCCATGTGAGACAAG	54476
rs559369567	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5766639	TCCAAATTCCAGAAC[C/T]GTGAGAAAATAAATT	54476
rs559372580	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5776814	GCTGAGGCACAAGAA[C/T]GGCTTGAACCTGGGA	54476
rs559393196	snp	A/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5633440	ATTAGCTGGGCCTGG[A/T]GGCGTGCACCTGTAA	54476
rs559395710	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5732821	GAGCTGATCTGACAT[A/G]CTAGCAGTTCTAGAG	54476
rs559396446	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5653332	GCGGTGGCTCACACC[C/T]GTAATCCCAGGAATT	54476
rs559413749	snp	A/G	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5702842	TGCTCAGTACGTGAC[A/G]GAAGGGAGGCTCACA	54476
rs559413827	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5709258	AGGTCTGAATATTAG[A/G]TATATGTTCCAGTCT	54476
rs559424954	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5723125	TCTATAAAATGATAA[A/T]AATGGCACATACATC	54476
rs559430019	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5775195	CTAGGCAACAACAAT[C/T]AGGATTTTCTTCAGT	54476
rs559435453	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713673	TTTCAAACAGCTCTT[C/T]AACATGAACAAAAAG	54476
rs559456813	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5751513	AAGAGTGAACAACCA[A/G]TTTCTTAAACAGGGC	54476
rs559486494	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5702038	ATTTCCTAGGGATCA[A/G/T]GGAGGTCGGCGACAT	54476
rs559508795	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5649845	TCTCACCAGAACAAA[C/T]AGCCCCTGGCAACTG	54476
rs559510314	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5643417	GCAGGATGTGCTCCC[A/G]GGGCAGGACAGGAAG	54476
rs559530366	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5628310	AAAATGACGGCACTC[A/G]GCTACAATGACCTAC	54476
rs559534528	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5684426	AGCTGGGCCTTCTAA[A/G]CCGAGCCTCTGCATT	54476
rs559538580	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5680081	GACCATGGATAGACT[G/T]CCTGCTGCAATCAGG	54476
rs559544224	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622630	GCGAGGGGAGGGGCA[C/G]TTCACATCGCAGCTC	54476
rs559545488	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5707168	TACTGTAGCTTTGTA[A/G]TAAGTTTTGAAGTCA	54476
rs559548689	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5646550	TACAAAAAATTAGCT[C/G]GGTGTGGTGGCACAC	54476
rs559549175	snp	C/G	0.00199481	0.0315187	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674717	CACTCATTTATAGTT[C/G]TGCAAAGCGGGGGGT	54476
rs559562832	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5623696	ACCTCTGCCTCCTGA[A/G]GAGCTGGGATCGCAG	54476
rs559569411	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5657922	CCTCTATTTTTCCTA[A/G]GTCAAGAATGCACAT	54476
rs559590736	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5771191	ACTATATGATGCTGT[-/A]ACTCAAAAGCCATAT	54476
rs559647364	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5637971	GTGCCTCAGGCTCCC[G/T]AGCAGCTGGGAGGCC	54476
rs559655917	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5642572	AAACGGTTCACATGT[C/T]TCAGCTTCCCAAGTA	54476
rs559658899	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5632515	CTCAAAAGAACAAGC[A/G]TAATGATGTGTCAGG	54476
rs559661676	snp	C/T	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5657534	ATCTTGCCATTGCAC[C/T]CCAGCCTGGGCAACA	54476
rs559664460	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713395	ACTGGAAACCACTCA[A/T]AGAGGAGAGCAGAGC	54476
rs559692301	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5637381	GCTAAGGGTTTCACT[A/G]GGTCATAAGCTTTGT	54476
rs559695221	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5631398	CTTGAGCCAGAAATC[G/T]AAGCTGCACATGGGG	54476
rs559697499	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5695372	GCCTGTCCTGACCTC[A/C]CACTCCCCAGTCTGA	54476
rs559711081	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5644569	GGAGTGCAGTAGTGT[A/T]ATATCAGCTCACTGC	54476
rs559735272	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5701838	GCTTCAAAAGAACTG[C/T]TGAAACAGACAACTT	54476
rs559750906	in-del	-/TATAA	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5755280	AGGAACCTATCACCT[-/TATAA]TAAAGTCCAGTGTTT	54476
rs559779243	snp	A/C	1.64781e-05	0.00287033	intron-variant	RNF216	GRCh38.p7	7:5760992	GGATGAAGTGAGAAC[A/C]AACAACTTACCTTGT	54476
rs559780814	snp	A/C	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5765776	AGTGAAACCCCGTCT[A/C]TACTAAAATACAAAA	54476
rs559786161	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5690344	AAAAAAAAAAAAAAA[C/G]ATTTTAAAGATCCTT	54476
rs559799864	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5771124	GATTCAGTCTTATAT[A/G]AATGTTTATGACAAA	54476
rs559820280	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5690258	CTTGCACACAGGAAG[C/G]GGAGGTTGCAGTGAG	54476
rs559821683	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5719828	TAAAAAGTGGCCAAT[A/G]CAGCTGCTTTGTGGC	54476
rs559828462	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736577	CGTCTCTGCCTGGCC[A/G]CCCATCGTCTGGGAT	54476
rs559863617	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712020	GCTGGCTCTTATCAG[A/G]AAACATAAGCACCAC	54476
rs559872648	snp	A/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5684043	TTTGGTCTGGCAGTA[A/T]CAGGTACTGGTCTGT	54476
rs559878753	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5699927	TAAAAGGCCTTTTAC[A/G]TTCTCAGCTACCACA	54476
rs559882474	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621431	GCTGGGATTACAGGC[A/G]GGAGCCACCGCGCCG	54476
rs559895654	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5732643	CCAACACAACTCTTC[A/T]GGAGGTTAAGTGACA	54476
rs559957063	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5746356	TTGCTCCCTCTTTGC[A/G]GAGGTCTTTACGGCT	54476
rs559963515	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5770845	CAGTGTCTTGCTCTG[C/T]CGCCCAGGCCGGAGT	54476
rs559968106	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5656126	ATACAAAAATTAGCC[A/G]GGCATGGTGGCGGGC	54476
rs559974450	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679308	GGCACTGGACTAAGG[A/G]CCTGTTTGTCACCAT	54476
rs559990819	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736325	TGGGGTTTCGCTGTG[C/T]TGGCCGGGCTGGTCT	54476
rs559997320	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662816	CAGGGAGGGTGCCAT[C/G]TGACACTGGTTTGTC	54476
rs560009045	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679174	CTTTTCAGGAGGATC[C/T]TGTCACCCTCGGGTA	54476
rs560025609	in-del	-/TTCT/TTCTT/TTCTTTT/TTCTTTTT/TTTTTTT			intron-variant	RNF216	GRCh38.p7	7:5759633	GAGTCATTTTTCTTC[lengthTooLong]TTTTTTTTTTTTTTT	54476
rs560033092	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5774906	GGCATGTTGCCACCA[C/T]GCCCAGCTAATTTTA	54476
rs560036797	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5717556	ACAGGGAATGATGTA[G/T]GCACAAACTTATCAT	54476
rs560049110	snp	C/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780481	GCGGAGGGATCACCT[C/G]AGGTCAGACGTTAGA	54476
rs560055833	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5755338	ACATGTAAGGTTCCA[A/G]TTAGCTTTTCAAAGT	54476
rs560065650	snp	C/G	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5722033	CTCAGGCAATCCTCC[C/G]GCCTCAGCCTCCTGA	54476
rs560075961	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5724471	TGTTCTGAACTCTGG[C/G]TAAATTTGGCTGAAT	54476
rs560078284	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668459	TGATTTCCTGACCTC[A/G]TGATCTGCCCGCCTC	54476
rs560085334	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5744619	ACCTCAAAGAATACA[C/T]TGGTTCTGAAGACTC	54476
rs560097366	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5765451	CCTAGGCAACAGGGT[A/G]AGACTCCATCTCAAA	54476
rs560124936	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5759654	TTTTTTTTTTTGAGA[C/T]GGAGTCTTGCCCTGT	54476
rs560138220	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750596	CCTATAAGCTGAAGC[C/T]GGACAAATCTACGCA	54476
rs560142042	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671736	CTTCAAACTGGAAGG[C/T]GGAGGTTGCAGTGAG	54476
rs560149743	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678631	AAGGAGGCCGGCACT[C/T]GTAGTGACAAATATC	54476
rs560164826	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652255	GCTGCAGAGATGAGG[A/C]AACAGAGGCTCAAGG	54476
rs560198197	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656995	ACAGGCCAAAGTCAC[C/T]GGGTTCTGTGTTTGT	54476
rs560210672	snp	C/G/T			intron-variant	RNF216	GRCh38.p7	7:5649997	ACATGCAGATAGAAC[C/G/T]TGGTGAACAGGAAGT	54476
rs560265071	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5773331	CACTGCAACCTCCAC[C/T]TCCTGGGTTCAAGCG	54476
rs560270307	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5745637	GGGCACGGTGGCTCA[C/T]GCCTGTAATCTCAGC	54476
rs560278225	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5647419	GCTTACTGCGGCCTC[A/G]AACTCCTGGGTTCAA	54476
rs560290143	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5700105	GACACAGACACCCAC[A/G]GGGACAGGGGGTGTT	54476
rs560293083	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5739146	ATGGTGGTGATAGTT[C/G]CATAATAATGTGAAT	54476
rs560308439	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5625642	CGCAAGGATTCTGGA[A/G]TTAGGAATTTCCTTC	54476
rs560309424	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5705768	CAACATTAGCCGGGC[A/G]TGGTGGCACATGCAG	54476
rs560330987	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5661746	AGGCAGAGGTTGCAG[C/T]GAGCTGAGATTGTGC	54476
rs560346730	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5621141	TCAAAGCCTCCATCC[C/T]GGGCAAAGGCAGAAA	54476
rs560355000	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5629465	ATCCTGTCTCAGAAA[A/C]AAAAAAGTGAAGATA	54476
rs560359606	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5749071	TCCAATGCCTTTTAG[C/T]TCACGTGACTTAGGT	54476
rs560363804	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5729183	TCACACTCCTGCATT[C/G]CACAGTAGAAGGTAT	54476
rs560370245	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5631470	ACTGGTCTCCAGTGG[C/T]CTCTGACCAGGTGCT	54476
rs560385120	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5661248	CCCAGCCCCTGCAGG[C/T]TGTTTTTCGAAGGGA	54476
rs560395527	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656576	CAGGGGGGAAGGAGC[A/G]TGCATGCTGGGTAGT	54476
rs560411634	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5638286	AAGCATATATAAAAT[C/T]TGACATATCTCCTGT	54476
rs560416394	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5703000	ATACCTGTAAGGGAG[C/T]GTCCTTCTGCGGCCT	54476
rs560417718	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5699658	TACAGAAACAGAGCA[C/T]GAACTGTTATTTAGT	54476
rs560423000	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5727069	CATGTCCTGTGGCTA[C/T]GCTGTTAGGGTGCAG	54476
rs560442072	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753912	AGGCAGGAGAATCGT[C/T]TGAACTCGGGAGGCA	54476
rs560449710	in-del	-/GA	0.0023933	0.0345097	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679824	TTAGACCCTCAGCAG[-/GA]GAGACTATCATGCTC	54476
rs560450382	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5720870	CCACAAACATAAGTA[C/T]TATGACAAAATCCAG	54476
rs560464238	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5731181	CGAGAAAACTATGAA[C/T]AAGTAAGAAGTGGAA	54476
rs560468706	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5651774	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC	54476
rs560485267	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5778977	TCGAACTCCTGACCT[C/T]AGGTGATCTGCCCGC	54476
rs560497043	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5711332	TGGAGATGCCACTAA[A/G]ATGCCCAGTTCCTCA	54476
rs560523313	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5757214	TAAAAATCCCCACTA[A/T]AATGGTGGATTTGTC	54476
rs560523552	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5629700	GGTGCAGTGGCAGGC[A/G]TCTGTAATCTCAACT	54476
rs560568100	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5630089	GGGGAAAAATAGAAG[C/G]AAAGAGGATGAGGAG	54476
rs560568138	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5734232	AAGTAGATGGAAAAT[G/T]TCATTGCTAAGTGGT	54476
rs560568427	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5766783	GAAACAGGGTCTTAA[C/T]TTCAAGTAACAAATG	54476
rs560583115	snp	A/C/G	3.45335e-05	0.00415521	intron-variant	RNF216	GRCh38.p7	7:5729610	AACTGAAATGAGAGA[A/C/G]AAGCATAAAATCAGA	54476
rs560606889	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5636274	CAGAAAACTGTGGTA[G/T]GCTGTGACTGTTCGC	54476
rs560613362	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5645842	TGATCCGCCCACGTC[A/G]GCCTCCCAAAGTGCT	54476
rs560630731	snp	A/T	0.000112784	0.00750862	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739491	TCTGTGTGTGTCTTC[A/T]AATTCAACACTAGTT	54476
rs560631064	snp	A/G			utr-variant-5-prime, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781621	TCAGAAGCCGCAGCT[A/G]CGAGCTCCGTGGCAG	54476
rs560644607	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5772986	GGTTTCACCATGTTG[A/G]CCAGGCTAGTCTCGA	54476
rs560645127	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5769656	TTGAGCCTAAGAGGC[A/G]GAAGTTGCAGTAAGC	54476
rs560665796	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5735441	TTATTGGTTAAAGAA[A/G]TTAAAAAAAGATTAA	54476
rs560692612	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5639356	TGCTAGCCCACCCCT[C/G]GGCTGTTCATCTCTG	54476
rs560711966	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5714623	ACCACAAACTCGGTG[A/G]TGTAAAACAATGTAA	54476
rs560749946	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5715393	ATTAATCCATACCTA[A/C]AACAGCGAGGTTTTC	54476
rs560754398	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5633847	GAGGTAGAATTTACC[A/G]GAGAGGTTTTAATTA	54476
rs560757469	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5660060	CCTGGGTGCAAGCAA[A/T]TCTCCCGCCTCTATC	54476
rs560766952	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5709807	TTGTCCAGGCTAGAG[A/T]GCAGTGGCGCAATCA	54476
rs560774079	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619921	ACTACTGGGCCTTCC[A/G]GGCCTGCTCCTGCCA	54476
rs560787461	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754310	ACAGGTGCACACTAC[C/T]TTGAACAGTTACTTA	54476
rs560791711	snp	A/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5778107	TTCTTTTAAACCACA[A/T]ATCTCACCATGGTGA	54476
rs560793405	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5736888	CCTCCGCCCGGCAGC[C/T]GCCCCGTCCGGGAAG	54476
rs560793888	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5682962	ACTCAGGAGCAAGCA[C/T]AGGTAAACCAACATA	54476
rs560810770	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5715880	CCGAGTAGTGGGGAT[C/T]ACAGGCACCCGCCAC	54476
rs560829458	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5725087	CACATGAATTTTCTA[A/C]CACCACACAAAATTT	54476
rs560865034	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768574	ATGCCGTAACAAATT[C/T]TGAAGGCTTGAAATC	54476
rs560867406	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5646360	GACGGGGTGACAAGG[C/T]GAGACTCCATCCCAA	54476
rs560878338	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5733837	AACATCATAACTCAG[A/T]ATTGTCGAAGAGTTG	54476
rs560901345	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5763517	CACCTGTAATCCCAG[C/G]TACTTGGAAGGCTGA	54476
rs560929076	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5692054	AAAGGTATAATTTCC[A/G]ACATTCCTACCCAGA	54476
rs560930745	in-del	-/TA			intron-variant	RNF216	GRCh38.p7	7:5751827	CTGGGATCTTTAAAC[-/TA]AAAAAAAAAAAAAAA	54476
rs560947370	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5698514	CCCGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	54476
rs560973821	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665892	AGACCAAGGCCGGGC[A/G]CGGTAGCTCACATCT	54476
rs560975862	snp	A/T	0.0178098	0.0926698	intron-variant	RNF216	GRCh38.p7	7:5758292	AAATTATGGCTACAA[A/T]CACTACCAAGTTAGA	54476
rs560999101	snp	G/T	0.00199481	0.0315187	upstream-variant-2KB	RNF216	GRCh38.p7	7:5781892	CAAGGAGCCACCATC[G/T]CCCCAGAGCTGAAAA	54476
rs561035180	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5660533	TTGACCTGGTGATCC[A/C]CCCATCTCGGCCTCC	54476
rs561047220	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5690882	CACATGTGTAAAATG[C/T]ACACATTCATCATGG	54476
rs561047312	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675367	TTTGGCATGGTGTAG[C/T]GGCTCATGCCTGTAA	54476
rs561060482	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5704466	TTTGCACAACTGAGA[A/T]AGGTAAAAGCGTATG	54476
rs561069673	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5647611	AGTGCTGGGATTACC[A/G]GTGTGGCAGCCATTC	54476
rs561084266	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782472	TGTCCATAATCCCCG[C/T]GCTTTGGAAGGCCAA	54476
rs561096083	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5723792	CCAAAGAGCAGTGTT[C/T]AGACGGAAAACAAAC	54476
rs561103722	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5742423	TGAAAGAATGCTAAC[A/C]CATCAGAAGAATAAG	54476
rs561111809	snp	C/T	0.00358779	0.0422022	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675897	TATTTTTAGTAGAGA[C/T]GGGGTTTCTCTATGT	54476
rs561113771	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670195	CGCCTCGGCCTCCCA[A/C]AGTGCTGGAATTACA	54476
rs561125834	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670657	GTTTCTTCATGTCCG[A/C]CAACCTAAGGTGACC	54476
rs561141229	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5695969	AACAGACTTCATTTC[C/T]TCACACAACAAGGAT	54476
rs561153673	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5696661	TGACTACTGCCCCAC[C/G]TCTCCCCTCTTGCCC	54476
rs561156295	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5703804	TTGCTTCATGAGTGT[G/T]CCTAAACCTCCACCT	54476
rs561177146	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768071	TTGCCGGTACTCTAA[C/T]TTGCACACCTAAAAA	54476
rs561195973	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681229	GTTTCTCATACTATG[A/C]CTAATGTAGGAACCT	54476
rs561212343	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5719761	TTTTGAGAAAATGCC[A/T]GCCAAATACCTATTT	54476
rs561215248	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5691441	GATGAATGCGTAAGT[A/G]TACAAGAGAGGTTTC	54476
rs561226330	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5752342	TTAAAGTAGCCTTGA[C/T]TATATGAAAAGACAA	54476
rs561230980	snp	A/C/T	1.64743e-05	0.00287	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741362	TGGCCTGATCATCTG[A/C/T]TAGAGCAGCTGACTC	54476
rs561237589	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5772725	CAAAACCAGGTTAGC[A/T]AAGTTTTACAACAGA	54476
rs561238617	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5654648	GCAGAGATGGCACCA[A/C]TGCACTTTAGCCTGG	54476
rs561246539	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5653418	CCTGGCTAACACGGT[A/G]AAACCCTGTCTCTAC	54476
rs561262762	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675162	GTAGTGATTCTGGAA[C/T]GCTCAAATAAGGTAC	54476
rs561305166	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669258	GTAAAGTTGAGAAGC[C/T]CTGACCTCTTTTGAT	54476
rs561306233	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5719209	AGCATGGGGAAACCC[A/G]GGCTCTACAAAAAAA	54476
rs561314869	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5746852	AAAAAGAGTGTTCAT[C/G]CAAGAAATTCACTTG	54476
rs561318193	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5702750	AAAGTGAAATTTTAA[A/G]AAGTGAAAACTGACA	54476
rs561326769	in-del	-/GTC	1.6473e-05	0.00286988	cds-indel	RNF216	GRCh38.p7	7:5652433	GGTACGGTACTTGAT[-/GTC]GTCTTTTTCAGCCAG	54476
rs561335926	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750116	TATCTGTCCTTTTAA[C/T]AAAAGGACACAACTG	54476
rs561346394	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5748095	GCAAATATCAGACCC[C/T]TCCCTAACTCTGATT	54476
rs561358559	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5649945	GAGGACCTTGATTAT[A/G]TCGTTCAATAGGATA	54476
rs561375426	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680649	CCTTGTGATCTGCCC[A/G]ACTCGGCCTCCCAAA	54476
rs561390820	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5633038	AGGCTGGAGTGCAGT[G/T]GTGCGATCTCTGCTC	54476
rs561392227	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674582	GCAGTGACCTATGAT[C/T]GCACCACTGCACTCC	54476
rs561417681	snp	A/G			intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5777503	TAGGGGGAGGAGAAG[A/G]ATACAAGACACTGAC	54476
rs561421701	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5658732	TGATTTATTTCATTA[A/C]ACCCTTTTAAATTTT	54476
rs561447154	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5633402	TCAACACGGTGAAAC[C/G]CCGTCTCTACTAAAA	54476
rs561448306	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5626940	TGGTGCACACTGGGA[A/G]ACACCCACAGTATTT	54476
rs561458277	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5766013	CTGGGCACAATGGCT[C/T]ACACTTGTAATCCAG	54476
rs561470090	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669361	TCTTTGCCACTGGCA[A/G]TCACAGGGAGGCTGA	54476
rs561472397	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5777103	GACCTGACACTACAC[A/G]TGGAGGGAAAGAGCC	54476
rs561483601	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5732765	AGTGGGGAAGCCTGT[C/G]GGACTTCAATCTGCC	54476
rs561487358	snp	C/T			upstream-variant-2KB	RNF216	GRCh38.p7	7:5782587	AGGCGTGGTGGTTCA[C/T]GCCTGTAATCCCAGC	54476
rs561491605	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643399	GGCAGGAAACACAGC[A/C]CCGCAGGATGTGCTC	54476
rs561509271	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5627810	CCCCTGATAAAACAC[A/G]AGGGACAAGAGAGGC	54476
rs561542289	snp	A/G/T			utr-variant-3-prime	RNF216	GRCh38.p7	7:5621583	GTGGCGGGCCACTCC[A/G/T]GAGACTGATGCAGCC	54476
rs561564879	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5728308	TTTTTGGCCAGGCAC[A/G]GTGGCTCATGTAGGT	54476
rs561565943	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5762016	TGTGTTCTCCAAGAA[A/G]TACGCATAATAGAAT	54476
rs561577230	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5654233	GTAAGACTGGTGGGT[A/G]TAGAGATGAGTCGCC	54476
rs561586908	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5751031	GGTTTTAGTTGGGGC[C/T]CTAGCCGAGGAGCAG	54476
rs561592293	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5776365	AAGGCGGGCGGATCA[C/T]GAGGTCAGGAGACGG	54476
rs561619816	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679259	GGACAGGCATCTGAA[C/T]ATGGCCATGCTGCTC	54476
rs561620874	snp	C/T	1.64806e-05	0.00287054	missense, intron-variant	RNF216	GRCh38.p7	7:5741700	AAATAGCTGCTCTTA[C/T]CTGATTCAAATGCTG	54476
rs561626118	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713317	TACCCGCTTCAGAAG[A/G]AATTGGCTGACTCTG	54476
rs561631994	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5653557	AGTGAGCCGAGATCG[C/T]GCCACTGCACTCCAG	54476
rs561635328	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5723579	GTGAACCCAGGAGGC[C/G]GAGTTTGCAGTGAGC	54476
rs561646941	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5684887	GAAGGAAAGGGTGCT[C/T]GGGAGTCCTGCATGG	54476
rs561649672	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5757220	TCCCCACTATAATGG[A/T]GGATTTGTCCAATTC	54476
rs561662742	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5708574	ATTACATGAGATACT[C/T]ATACTTTATTCTAAA	54476
rs561744895	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5707884	GCGCACGCAACCACA[C/G]CCAGCTAAATTTTTG	54476
rs561760605	in-del	-/C	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5659705	CTAGGGGAACAGGCT[-/C]GGAGTGTGGATTTGA	54476
rs561761799	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736278	GCGCGCCGCCACGCC[G/T]GACTGGTTTTCGTAT	54476
rs561774769	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5756397	AGTTGCAACAGAAAC[A/C]ATATGGCCCGCGAGG	54476
rs561781865	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5731264	ATGAAATATAAAAGA[C/T]CTTCTGTTAATTCAT	54476
rs561783721	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669055	AAAGAGCATTAGAGA[A/G]TATTTCAACGCAGGC	54476
rs561803688	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5685780	GGGAAAAGAGCTTTA[A/G]ATATTCAAAGCCCCA	54476
rs561813616	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5746510	AAACTCAGGCTTTTG[C/G]AATCTGTGGGTATGT	54476
rs561821996	snp	C/T	0.00597247	0.0543191	intron-variant	RNF216	GRCh38.p7	7:5723057	CAGCTGGGCTACTCG[C/T]TAGCTGTGTAACATC	54476
rs561835312	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5751355	GTTAAATAAAAATTA[C/T]AGGAGGCCACTGTTT	54476
rs561837495	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5770847	GTGTCTTGCTCTGTC[A/G]CCCAGGCCGGAGTGC	54476
rs561842032	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5657070	ATGCGTGCTAGATTT[C/T]AGTTGCTGACTTCCA	54476
rs561845081	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663452	AGCCAGGTGTGGTGG[C/T]GTTCGCCTGTAGTCC	54476
rs561851353	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5702176	CAGTTGCCTCTGCGA[A/G]TTTCGAGGGGAGAAA	54476
rs561856497	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652358	CTCTACCAAAAAGCA[C/G]GTTAATGGGGAAGTT	54476
rs561863147	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622015	CCTCCCCCAGAAAGC[A/C]AGGGGGGAAAAGCTG	54476
rs561864218	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5648885	TGAACAAACTAACTG[C/T]AGTACACATGTAAAG	54476
rs561871678	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5690795	ATGCCCCGACAGCCT[A/G]CAGGGATGTACACAC	54476
rs561877372	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5623247	AATCTAGCCTGGGAC[C/T]AGGGCAGCGACCTCT	54476
rs561905961	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5716985	CAAAATGTAGAATAA[A/G]TAAGGGAAAAGGCTG	54476
rs561914168	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5641647	GTGTTTTGAGAATTA[C/T]AGACAAAATATAAAG	54476
rs561914878	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5690283	AGTGAGCCAAGATCG[C/T]GCCATTGCACTCTAG	54476
rs561927287	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5685397	CTCCTCCCCACAGAA[A/G]CCCTGGGATGGAAGC	54476
rs561942877	in-del	-/T	0.00358779	0.0422022	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620596	AGGAATCAGGGACCC[-/T]CCAAGGAAAGAGGCC	54476
rs561949875	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5642100	TGAGGTTTAGATAAA[C/G]TGCATTTAGTACTAT	54476
rs561950054	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5717718	ATGAATTGCTGCAGA[C/G]TGACTGCCAGGATGC	54476
rs561957137	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5701345	TTTTCCACCTGCCCA[C/T]TTTAGGGGAACTCCA	54476
rs561959610	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5632450	GCCAGGCTGAGGTGA[A/G]AGGGAGTGGATGCTG	54476
rs561972502	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668338	ACACCATTCTCCTGC[C/T]TCAGCCTCCCGAGTA	54476
rs561975035	snp	A/C/G			intron-variant	RNF216	GRCh38.p7	7:5642442	TGGTCTGGAACTCCC[A/C/G]ACCTCAGGTGATCCA	54476
rs562000009	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5627088	CCCAAGGGACACTTA[C/T]GGCCTTCGATGGCAC	54476
rs562007053	snp	C/G	1.65135e-05	0.00287341	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712673	GGTAGTTTTCACAAT[C/G]GGGAAGAGTTGGCAG	54476
rs562007546	snp	A/G	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5648384	AGTGCTGGGGTTACA[A/G]GCGTGAGCCACTGTG	54476
rs562036788	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662775	TCAGAGGAAACTAAA[A/G]CCAGGTAGGGGGCAG	54476
rs562047890	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5729750	GACAGATGAGAAAAC[A/G]GTGGCTCAGAGAGGT	54476
rs562058984	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5700881	CCAATGCACCAAGAA[C/G]ACAAACCCTGGATTT	54476
rs562063118	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5770810	ACAGATTCTTTTTTT[C/T]TTTTTCTTTCCCCCC	54476
rs562099995	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711527	TGTCCTAAAGAAGAT[A/G]ATATAAAATAGGAAT	54476
rs562107531	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5743350	TCTATAAACTCTATC[A/G]AAAAAGGGCATATAC	54476
rs562110256	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5745080	ACACACAAACCTACG[A/G]GCCAATCTCCACCTG	54476
rs562116775	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5721512	GGTTAATCTGAATAG[C/T]GCTGCTTATAGCCAT	54476
rs562137014	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5694244	GGAACAGTTTTCAAA[C/T]AAGTCTTTCAGCTTC	54476
rs562149400	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216, RNF216-IT1	GRCh38.p7	7:5662359	CCGCATAAACAGAGA[C/T]AGGCTCCATGAAAGT	54476
rs562153695	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5779438	ATAAATTATGAAATA[A/C]AAAACCAAGGCAAAG	54476
rs562159512	in-del	-/G			intron-variant	RNF216	GRCh38.p7	7:5730910	AGAATATAGTCCTTA[-/G]TCACACATTACAACT	54476
rs562174889	snp	G/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753560	TCTAACCATCTAAAT[G/T]TAGTAATTCTATTCA	54476
rs562195342	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5695329	CATTCACACGTCCAG[C/T]AGCCACAGAGACGAA	54476
rs562206380	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667248	TTTTATAAAACTGTT[C/T]CTGTTCCACCTATAT	54476
rs562229669	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5721733	TTAGCCATTCTGGTG[A/G]GTGCAAATGTGCTGT	54476
rs562241035	snp	A/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5774164	TCTGGGCTTCGGATA[A/T]TACTGCCTATGTTTA	54476
rs562277999	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5632976	ACCCAGCGGAACTGG[A/C]AGAGCACTTTCTGTT	54476
rs562285025	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5779527	AGAATCTTCCCGCTT[C/G]TCTCCCTTCTCAGCG	54476
rs562286361	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5631569	CATGTTTTCTCCTGA[C/T]ACTACCAAGTTACTT	54476
rs562298204	snp	A/C	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5709390	CCCCAGCCTTTGATG[A/C]AACTGGTTTCTGGAT	54476
rs562310718	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5721282	TTCTCTCTGATGGTA[C/T]GTTTCATGACTTTTC	54476
rs562316423	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5651470	TTCGTGAGCTCAAGC[A/G]ATCTACCTGCCTTAG	54476
rs562324542	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5625117	GCTAAGGTGTGGGCC[C/T]GAGGGGGCTGAGGCT	54476
rs562326883	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5627702	CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA	54476
rs562328110	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5711962	ACATCCCCTTTATAC[G/T]CCTTAGTTTTCCTTA	54476
rs562337394	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5705584	ACATCCCTCTTGGCA[C/G]AGGGAAAAAATGAAC	54476
rs562338837	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5688750	TTTGGACTGGGATAT[C/G]TGTAAAACTGTGGGT	54476
rs562353059	snp	A/G	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5683394	GCAGCTTCCAACTCT[A/G]TTTTCCTGCAACAGT	54476
rs562361398	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5699417	AAAGCCCCTAAAACC[C/T]AGGAAGAGTTTTATT	54476
rs562373365	snp	C/T			intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739600	ATCCATTCTTCATTG[C/T]TTCAACAAATATTGA	54476
rs562384645	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5649330	CTGGGAGGCGGAGGT[C/T]GCAATGACCCGAGGC	54476
rs562397568	snp	G/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5740097	TAGTGGCTACCAGAT[G/T]TAACACCTTTTTTTT	54476
rs562437094	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656517	AACCACGGAGTTCAC[C/T]GTCATCCCAAATACA	54476
rs562438266	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5706776	GCTGAAAGCATCTTA[A/G]TAGTCACTTGCCTGT	54476
rs562472512	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5693718	CCCTGTGCTTGTGTT[G/T]TTCTAAAGTTAGGCA	54476
rs562479261	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5726012	CTGGGTGCAGTGGCT[C/G]ACACCTGTAATCCTA	54476
rs562513151	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5689131	CCTTGTGAGCCAATA[C/T]GCAGAACCAAAAGCA	54476
rs562526009	snp	G/T	0.100231	0.200173	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676028	TCTTTTTTCTTTTTT[G/T]TTTTGAGACAGAGTC	54476
rs562550798	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750248	TGTCTCTTCCTGGCA[G/T]GCTCAGGAACCTCCA	54476
rs562560725	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5760761	TCAATGACTGCATAT[G/T]AACAGCGTCTTGCCA	54476
rs562578599	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5763955	GCACCTTGGGAGGCC[A/G]AGGCAGGCGGATCAC	54476
rs562586305	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5651735	CTCACTGCAACCTCC[A/G]CCTCCCGGGTTCAAC	54476
rs562617182	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5772872	AACCCTCTGCATCCC[A/G]GGTTCAAGCAATTCT	54476
rs562632906	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5646977	TGTTGAGCCCTAGAC[A/G]TGTACGTAGTCTTCT	54476
rs562638202	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5730412	TTGGCCAATTCTTGT[C/T]TTGCTTTAGGAATTT	54476
rs562653908	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5773234	TCAAGTCCTTTTTTT[C/T]CCCCAAATAAGATTT	54476
rs562655633	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5705681	TGGGAGGCCAAGGCA[A/G]GCAGATCACCTGAGG	54476
rs562656284	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5759160	AGCCATGTGAGACAA[G/T]CGTGCTTCCCCTTTT	54476
rs562713004	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5655289	CAGCCAGGGCGCTTC[C/T]TACTGAAGGGCCCGA	54476
rs562735150	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666596	GCATGAGGTTGATTC[C/T]CAAAGAACCCCACCT	54476
rs562745490	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675642	CAAGACCCTCTCAAA[A/G]CAAACAAACAAACAA	54476
rs562763116	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5625331	AGCAAGTCCCAACAA[C/T]GCAAGCAGTCTAATG	54476
rs562780477	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656174	CTCTGGAAGCTGAGA[C/G]AGGAGAATTGCTTGA	54476
rs562800253	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5635868	ACCAAATGGCTAGGC[A/G]ATAATTGTACCAAAT	54476
rs562803965	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671475	TTAAATGAGGCTGAT[A/G]GGGTGAGCGCTATTC	54476
rs562807591	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5722095	CACCCAGCTAATTTT[C/T]TTGTATTTTTTTAGA	54476
rs562812785	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681907	TGTGTAGCCCCTAAG[C/G]GTGGTAACCCCCAGT	54476
rs562820364	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5710351	GGCAACAGAGTGAGA[A/C]CCTGCCTCAAAACTT	54476
rs562837941	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5639656	ATTAGAGACAGGTTT[C/T]ACCATATTGGTCAGG	54476
rs562861135	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666018	AAAATACAAAAAAAT[C/T]AGCCGGGCGTGGTGG	54476
rs562883196	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5705269	AAAAACTCAACATGT[C/T]CAAAACAAAAGTAAT	54476
rs562931808	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5692604	AGGAGAAAGGCAGAG[A/C]TGCTCAGTTCCAGCT	54476
rs562958080	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5733273	TTTGGATTTCACGAG[A/C]ATTTTAATGTGTTTA	54476
rs562958146	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5737964	AGGGTGGAGTACGCC[G/T]GTAATGCCAGCTACT	54476
rs562959655	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5738640	CTGAACCTGGGAGGC[A/G]GAGCTTGCAGTGAGC	54476
rs562987764	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5744478	AGGGAAGGGAAGGAG[A/G]GGGACACATAATGGT	54476
rs562994728	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5733716	AGTAAACAATTCACA[C/G]GCAAGGGAAATACAA	54476
rs562998420	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5739126	TGAAAGAGTTCTGAA[C/G]ATGGATGGTGGTGAT	54476
rs562999840	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712547	CAATGGTTCTGAGGC[A/G]TAAAAAATAAAAATA	54476
rs563039039	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5659450	GAGGGTCCGTCTCAT[C/G]CTGAGAAAGTCAGTA	54476
rs563039857	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5710636	GTGCTGCATGGGCCT[A/G]CCCCTACTCAGCTTA	54476
rs563051044	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5654875	CTAACTATTACCCAC[C/T]GAAACATACAGCAGC	54476
rs563064429	in-del	-/AGG			intron-variant	RNF216	GRCh38.p7	7:5726980	GCCTGCAAGAGAAGA[-/AGG]AAGAGTGGGAGCCTT	54476
rs563091011	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674176	CTGGGATTATAGGCA[C/T]CCACCACCACGCCCA	54476
rs563105752	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5719525	TTAAGAGAGACTAAC[C/T]TGAAGGGGCAGCCAA	54476
rs563120739	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5633825	GCTGCACTTGAAGAC[A/G]GCAAGTGAGGTAGAA	54476
rs563149163	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782583	GGCCAGGCGTGGTGG[C/T]TCACGCCTGTAATCC	54476
rs563168046	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5763438	GAGTTTGATACTAGC[C/T]GGGCCAACGTGGTGA	54476
rs563169338	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5687940	CGTGTCCAGAATCCC[A/G]GACTGTCATGCCACA	54476
rs563171830	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664702	AAGGGTAGGCTGCAC[A/G]CTTCCCCCACTGGCC	54476
rs563177151	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5720862	TTATGAAACCACAAA[A/C]ATAAGTATTATGACA	54476
rs563185655	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5725053	CCCAAGCTTAACAGC[A/G]CACTCAAATACCTTC	54476
rs563188407	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668414	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT	54476
rs563221807	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5714877	TGTGCCCTGAAAAGA[A/T]ATCTGCTGTGCTCAG	54476
rs563252739	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5763061	ACTACTGAACTCTGG[A/G]GATAGGAAACAGAGA	54476
rs563269386	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5737497	AATCCCCCTCTGCGA[C/G]AAACAACCAAGAATG	54476
rs563270748	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5646940	AGGTGAAAGCCTAGG[C/G]TCTTGGGTTTTTCTG	54476
rs563272747	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5624288	TCCTTCCTATTTCCC[C/T]GAAGGCCTCCTTCCT	54476
rs563287054	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5638970	ATTTTTTTAAACTTC[C/T]TCTGTCCATTTTTGA	54476
rs563290453	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5704369	TCAAAATTAGCTTGT[A/G]GCTCATGTCTTAAAT	54476
rs563322999	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5762602	GAAGCTAAGGCAGGA[A/G]AATGGCATGAACCCG	54476
rs563326120	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5781811	CCGGGCTCTCCGCCT[C/G]CGGAGACTTGACTCC	54476
rs563331700	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5644742	ACTCCTGGGCTTAAG[C/T]TATCTGCCCGACCTT	54476
rs563331960	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5696577	CGCGTGCCCAAGATC[A/G]TGTCCTATGGTCTCG	54476
rs563335481	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5623709	GAGGAGCTGGGATCG[C/T]AGATGTGTGCCAACA	54476
rs563340482	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5748027	TCCCTAAATTCCTAT[A/G]CTCCAAGAAAAATCA	54476
rs563357762	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5629614	CGGGCGGATCACGAC[A/G]TCAGGAGTTTGAGAC	54476
rs563388658	snp	C/T	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5777680	GAAAGAAAACGAAAA[C/T]TGTGTTAACTTTAAT	54476
rs563394070	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665204	GGGATTCCTCTCTAT[C/T]CTCAAAGTACAGTAA	54476
rs563425502	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5742344	GAGCCACTGAACCCA[C/G]CCCTGAATTATAATT	54476
rs563426856	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5692184	GAGGGAACTATGAAT[C/T]GAGGCTGGCAGCCAA	54476
rs563430477	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5723539	GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGTAG	54476
rs563440263	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5752678	ATCCAGAAACAGACT[C/G]AAACATACAGCTTCT	54476
rs563444798	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5719092	TAGCATCAGAGAAAA[A/G]AAAGTTGGCAGGGCA	54476
rs563452675	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5651053	TACGAGCGGAAGTGA[C/G]ATATATGTATATAAT	54476
rs563456088	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670068	ATTAGCTGGGATTAC[A/G]GGCACGCACCACCAT	54476
rs563460626	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680590	TTGTATTTTACTAGA[A/G]ACGGGGTTTCACCAT	54476
rs563461784	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713784	ACTAGCTAAAATTTA[C/T]GAGGCATTTACCATG	54476
rs563498538	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5741941	TCCCTTAACAATACC[G/T]ATTCTTTACATTTAT	54476
rs563521972	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5723516	GCCGGACTCGGTGGC[A/G]GGCACCTGTAGTCCC	54476
rs563524082	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674954	GTGAGCTGAGATCGC[A/G]CCACTGCACTCCAGC	54476
rs563527087	in-del	-/A	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5689572	TCTTGGACTTCCTAC[-/A]AGTTTTTAAAGCATA	54476
rs563528727	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5732928	ACTGAAGCTGACCAC[A/G]TGTGAGTGAAAGGTC	54476
rs563536054	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5771188	TTCTACTATATGATG[C/T]TGTACTCAAAAGCCA	54476
rs563546608	snp	A/G	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5776980	AAAAAGAAAGTGAAA[A/G]AAAGGAAGAGAAAGA	54476
rs563554373	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5702087	GCCGGGTTCTCGGAG[C/T]CCACGCTGACTCTAG	54476
rs563559632	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5728239	CCTTGGTCTACCTTA[C/G]GTTGCCTCCCGTTTT	54476
rs563585429	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5772043	GTTCGAGACCAGCCT[C/G]ACCAACATGGAGAAA	54476
rs563597084	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5627698	GTTGCAGTGAGCCGA[A/G]ATCGCGCCACTGCAC	54476
rs563604607	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5686376	TCACAACCACCCTGA[A/C]GGGGGCTGGGACAGA	54476
rs563611135	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5654143	GCCACTCAGGAGAGA[A/G]GCCATGAAGGCCCAG	54476
rs563628075	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5756680	GGCTAGAGTACAATA[C/G]CATGAACACAAGTTC	54476
rs563641637	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5658604	GGAGGTTGCAGTGAG[C/T]TATGATCAAGCTACT	54476
rs563645461	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5633485	GAGGGTGAGGCAGGA[A/G]AATCACTTGAACCCA	54476
rs563652036	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5692451	CAGCAGTTGGAAACA[A/G]TCTTGAATTCTAACT	54476
rs563654605	snp	C/T	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5702928	CCAGTGTCTATTTTG[C/T]AGGGCTGCTGTGGGG	54476
rs563663788	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5649446	CTCAGGAGGTCAAGG[A/C/T]TAAGGTTAGCTGTGA	54476
rs563669051	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5653816	GATGAATAGGGCGGC[A/G]AAAACAGATCAACAC	54476
rs563682159	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5707801	CAATCTCTGCTCACC[G/T]CAACCTCCACCTCCC	54476
rs563715445	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5757079	TCATTGTGATTTCTT[C/T]TCACACTGGGTGCAG	54476
rs563723867	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678742	GCACTGTGAGAGCTA[C/T]AGCAGTGGGACAAGC	54476
rs563752141	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5752200	AAAAAATAAAAAAAA[A/T]GAAAGTACAATGAAA	54476
rs563757840	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669028	TTTTTAGTTCTGTGG[A/G]CCTAATATTATAAAG	54476
rs563777281	snp	C/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5716313	TCAGGAGTTCAAGAC[C/T]AGCCTGGCCAACATG	54476
rs563790125	snp	A/G			intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652132	TAAGTTAATTAAAAC[A/G]CGTTACTTGCTTATT	54476
rs563842508	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673515	GTGAAGAACAGCAAA[A/G]CTGACCTGTCACGTG	54476
rs563847850	snp	A/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5775807	CCGGGATGCAAAGCT[A/T]GCAGTGAGCCTAGAA	54476
rs563848128	snp	C/G	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5770864	CCAGGCCGGAGTGCA[C/G]TGGTGTGATCTCGGC	54476
rs563853037	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781267	GACCCGAGGGGCCGG[A/C]CCGCGAAACTTCGCG	54476
rs563857948	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5637848	ACCAGGCCAAATTAC[C/G]CATTTCTTTTTCTTT	54476
rs563859120	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5759462	ATATTTTCTTTCTCT[C/T]CCTTATGATTTTCTT	54476
rs563862992	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5732688	AAATGAAGGACAAAG[C/T]TTTTCTTCTACAGAA	54476
rs563880919	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5707353	AGTCTTTACCCACTC[C/T]TTGGTTAAGTTGTTC	54476
rs563884234	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736612	GGAGCCCCTCTGCCC[A/G]GCTGCCCAGTCTGGG	54476
rs563901847	snp	A/C/T			intron-variant	RNF216	GRCh38.p7	7:5699867	GTGACAGAGACCCTC[A/C/T]GTATTCTTTATCTTT	54476
rs563905030	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662968	TCAGAGAATCCAGCA[A/C]CCACACCCCCTATGC	54476
rs563982019	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5760873	ATTCTAGTCTAACTA[C/G]TCTTTTTGTCAAAAA	54476
rs563994904	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780600	TGAGGCAATCCCTGT[A/G]AGGCTGAGGCAGGAA	54476
rs564014587	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5684715	ACCCTAGCAGCAATT[C/G]CAGTGGGTGTTCAAG	54476
rs564018794	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5755912	CATCTGCAGTGTAGG[A/T]TAGTACGTTGCTTCA	54476
rs564022202	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5727702	CCACTGTACTCCAGC[C/T]TGGGTGAGAGAGAGA	54476
rs564026365	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5761525	AGACGCAGTGGCTCA[C/T]GCCTACAATCCCAGC	54476
rs564033701	snp	A/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5717587	GGCACTATTTATAAT[A/T]GCAAAAACCTGGAAA	54476
rs564042091	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674356	TACAGATGGGATTTC[A/T]CCACATTGGCCATGC	54476
rs564046087	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5707341	TTTCAGTGTATAAGT[C/G]TTTACCCACTCCTTG	54476
rs564075350	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750914	ACAGAGAAGATTCTG[G/T]GCAGTTGATGGCGCT	54476
rs564102689	snp	C/G	9.89462e-05	0.00703302	intron-variant	RNF216	GRCh38.p7	7:5729417	TGACCCCAACAGGAA[C/G]ACCAAGTAGAGTACC	54476
rs564111131	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5703227	CCAGCTATTTGGTTC[C/T]TGTCAACGCTACTTC	54476
rs564111622	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5746388	GAGTCAAGCCCCCAA[A/G]ATTATGGCCAGACAG	54476
rs564114771	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5739697	AGCACACAACCTAGT[A/G]CCTAGATAAAAACAC	54476
rs564158510	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5740740	AGCACCAGGCCACCA[C/T]GATATGCAGTTAGAA	54476
rs564168174	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667229	TCCATGTGTCAAGTA[C/T]TTGTTTTATAAAACT	54476
rs564168423	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673654	GAATAAAACACCCCA[C/T]ATCATCACAGCAAAT	54476
rs564189095	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712621	TCAAAAAACCTGGAA[G/T]ATAAACACAATTTTC	54476
rs564201860	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5750640	AAGTCTCATGCCTAA[G/T]GCATGGGCCACACAG	54476
rs564214088	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5726973	CCATTCCGCCTGCAA[A/G]AGAAGAAGGAAGAGT	54476
rs564224643	snp	A/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5717120	GCACTTTGGAAGGCC[A/G]AGGTGGGCAGATCAC	54476
rs564228453	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668500	AGTGCTGGGATTACA[C/G]ATGTGAGCCACCGTG	54476
rs564233704	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667727	CCAGCTCCTGCCTGC[A/T]GGAACTCCACTGTCA	54476
rs564238152	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5735857	CCCAGCACTTTGGGA[A/G]GCCGAGGCAGATGGA	54476
rs564246329	snp	C/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF216, RNF216-IT1	GRCh38.p7	7:5662258	TCAGACTGGACACGT[C/G]TGAGGAAGTAGCTGT	54476
rs564247108	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5658055	ATGTGCACGCACACA[C/T]GGCAGGGGAGCATGC	54476
rs564252596	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5637532	CAAAACCATGAGTAG[C/T]TCTCAGGATTATACA	54476
rs564266339	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5621198	TTTTTTTTAAAGATA[A/G]AGTTTTGCTTTTGTT	54476
rs564273070	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5657058	GTGTCCGTCCCCATG[C/T]GTGCTAGATTTCAGT	54476
rs564276648	snp	C/G			downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619619	GTGTCTCACCAGTCA[C/G]GGAAGGGACTCAAAT	54476
rs564276973	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5642299	CTCACTGCAACCTCC[A/G]CCTCCCCGGGTTCAA	54476
rs564300912	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5726549	CTGTTAGATTTCCCT[C/T]ATCAGGATTTAAATG	54476
rs564314766	snp	G/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5769708	CAACCTGGGAGACAG[G/T]GAGAGCTGTCTCAAA	54476
rs564318069	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5689841	GCCACTTGGGAGGCT[A/G]AGGCAGGAGAATCAC	54476
rs564325182	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5651135	ATTTCCCACTTTCTT[G/T]GGGTTTGAGTGTAAA	54476
rs564360342	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5722208	GGATTACAGGTGTGA[G/T]CCACAACGCCTGGCC	54476
rs564373808	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5722653	CCTCGGCCTCCCAAA[A/G]TGCCAGGATTACAGG	54476
rs564378675	snp	A/C			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5711992	AAAAACACAGATTGA[A/C]CCTCTTCTTTGTGCT	54476
rs564385480	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652316	CTGGGGTGGCTCAAG[C/T]GTGTTCTTCCGACAA	54476
rs564388516	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5744669	CAAAAAACAACCCTC[A/G]AAGAAATAAAGAAAA	54476
rs564405663	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5647555	CCCAGGCTGGTCTTC[A/G]ACTCCTGGGTTCAAG	54476
rs564423722	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5745002	AAAAAGAAAACTTCT[A/C]AACTTTTTATGAAGT	54476
rs564429081	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656679	CTTTTGTCCTCAAAA[C/T]ACATTAAGGTGTTTT	54476
rs564441835	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5709481	AGGGTCTGGAGCTTT[C/G]TCTTCTGTCATCTTG	54476
rs564449762	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5694428	TCTGGGTAATAACAT[C/T]TGACCTTGAAATCCC	54476
rs564487031	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5700146	CGGTATTACCATAGC[A/T]ACAATTTCTCTTCTA	54476
rs564487553	snp	A/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5641462	TTATTTATTTTCACA[A/T]AAAATGATCACTTAT	54476
rs564490628	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5715960	GTTGACCAGGCTGGT[C/G]TCAAACCCCTGACCT	54476
rs564509984	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5772584	AACCACTGTGCCTCA[A/G]AGGCAGTAAGCCCCA	54476
rs564529290	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5625751	ACAGAAAGGCAGATG[G/T]ACTGAGTAAGTAATT	54476
rs564534025	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5770259	CTGAGGTGGGGAGTT[A/T]GAGACCAGCCTGACC	54476
rs564535091	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5624770	TCCAAGCCTCAGACA[C/T]GAACCGAAGAGGCAC	54476
rs564550662	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5700609	ATAGCTAACTAGTAC[A/C]CAAAACCACAAAAAG	54476
rs564563206	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677458	AAAACAAAAAGGAAA[A/G]CTAGAAGAAAAAATG	54476
rs564564924	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5685628	GGGGAGGGGGCATAG[C/T]GGAAAAGGAAGTAAA	54476
rs564586013	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5734111	CACAAACATAGCCAA[C/T]AGGAAGGTGGATGCC	54476
rs564619477	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5731217	TGTGTTCACATTTAC[A/G]GTAAAAAACAGTCTG	54476
rs564628385	snp	A/C	0	0	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754659	TAAGACCCCTGCACC[A/C]GCAGGAAATTGTAGA	54476
rs564629138	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5725548	GCTGTCTACCCAGCA[A/T]GGCTAACAATTGGTA	54476
rs564660145	in-del	-/G	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5719789	TTTTGAATAATCATA[-/G]TTTTTCTGTCACTTT	54476
rs564675813	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5635694	CGAGGACAAATGACC[C/T]GGGTGGAAACCCAGG	54476
rs564690900	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5710295	AAGCCAGGAGGCGGA[C/G]GTTGCAGTGAGCTGA	54476
rs564727379	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678572	AGGTGAGTGACCTCA[C/T]CTCTCCCAGCTTCAG	54476
rs564740536	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5778995	GTGATCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC	54476
rs564749163	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750199	GCAAACAATGCCTGG[C/T]TTTAAGCATTCCCTG	54476
rs564753351	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5705231	GGCATTGTAAAAACA[C/T]GTACACACTGGATGT	54476
rs564755013	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677978	AAGACCACAGTGATC[G/T]TTCCAGGGGGTAACC	54476
rs564759475	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5629774	AGAGGCTGCAGTTAG[C/T]CGAGATGGTGCCACT	54476
rs564760360	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620342	GCAAGCCCTGCAGGG[A/C]AGAGAGAGGGAGCCA	54476
rs564777929	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5720546	TTTCAGCTGCACAGG[A/G]GGAAGCACTCCTAAC	54476
rs564798334	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5630157	TGCTGTCTCGGGGCT[A/G]AGTCACAAACAGGAA	54476
rs564816402	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672384	CCACTCTGCAAAAAC[A/G]CCAAGTTGGAGAGTT	54476
rs564820114	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5775925	GGCTGGAAGAAGATG[A/G]CATGCCCGTGTCACA	54476
rs564820542	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5756391	CTGAATAGTTGCAAC[A/G]GAAACCATATGGCCC	54476
rs564833145	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5660981	TTTGAAACAGCATCT[C/T]GCTTTGTCACCCAGG	54476
rs564838078	snp	C/T			intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739486	GCAGGTCTGTGTGTG[C/T]CTTCAAATTCAACAC	54476
rs564839174	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5718852	ATGAGCCATCCCACC[C/T]GGCCAAACTTAAGTT	54476
rs564850184	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754335	TACTTAAAAAAAAAA[C/T]TTTTTTTTGTAGAGA	54476
rs564868932	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5763848	AAAGTGCTGCGATTA[C/G]AGGTGTGAACCACCA	54476
rs564885481	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5688132	GGATTCCCACAGTTG[A/G]CTGGTGGGGACACCA	54476
rs564890723	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5778991	TTAGGTGATCTGCCC[A/G]CCTCGGCCTCCCAAA	54476
rs564895374	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5699232	TCCCAGATTACAAAT[A/C]TTTTCATTTATAAAT	54476
rs564907651	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5759071	CCGTTCTGGTTGCAA[A/C]AGTGAGTTCTTGTGA	54476
rs564912065	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681347	AAAAAATACAAACTT[C/T]ATTCTGAAAGAGAAA	54476
rs564914076	snp	A/C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5687301	CTTGGGAGGCTGAGG[A/C/G]GGGAGAATCACTTGA	54476
rs564916747	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5634420	TAGTTTCAAATTATT[A/C]CCAGATTAGCCACAG	54476
rs564920310	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782508	GAGGATCGCTTGAGG[C/G]CAGGAGTTCAAGACC	54476
rs564937819	snp	C/T	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5688655	TCACTCTGCGCACCT[C/T]ACCTTGCTTTACACA	54476
rs564949166	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620612	CCAAGGAAAGAGGCC[A/G]CCGCTCCTTCCCCAC	54476
rs564971030	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656138	GCCGGGCATGGTGGC[A/G]GGCTTCTGTAATCCC	54476
rs564984194	in-del	-/CAAAA			intron-variant	RNF216	GRCh38.p7	7:5646372	GGCGAGACTCCATCC[-/CAAAA]CAAAACAAAACAAAA	54476
rs564990995	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5683920	ACAGAGAATAGGGAC[G/T]GGCATCACTTGTGTC	54476
rs565007947	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5777560	TGTATGTCACTGGCC[A/T]TCAGGGCAAGAAGAA	54476
rs565009934	snp	A/T	0.00914312	0.0669923	upstream-variant-2KB	RNF216	GRCh38.p7	7:5783049	TACAAAAATAAAAAT[A/T]AGCCGGGCATGGTGG	54476
rs565015973	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5629303	GCAACACAGTGAGAA[C/T]CCAGCTCTACAAAAT	54476
rs565032034	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5651395	ACCACTCCTGGATAA[C/T]TTTATTTTTTATTTT	54476
rs565047570	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5730035	ATAATGACAATGATT[A/G]AAGTTTTTAAAAACC	54476
rs565077148	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5639957	GTAGAGACGGGGTTT[C/T]GCCATGTTAGCCAGG	54476
rs565077524	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5709863	GGGCTCAACTGATTG[C/T]CCTGCCTCAGTCTCT	54476
rs565100593	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5720200	CAGAGATGTGAACTG[C/T]GGGGACCCACTTATG	54476
rs565105904	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665453	TTTGAAAAAAGAAAT[C/T]TTGAAGTGTTATTTC	54476
rs565112190	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5634897	GGGTAGCAAAACTGC[C/T]AGGGCCCCTTTCTAC	54476
rs565164177	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5652521	GTTTCCTGGGGATAA[A/G]GGACAGACACAAAGA	54476
rs565184369	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675961	TGATCCGCCCACCTC[A/T]GCCTTCCAAAGTGCT	54476
rs565191947	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5769027	GTTAACTATTTTGAC[G/T]AAATAAACTGAAAGA	54476
rs565214835	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5714686	CAGAGAAACTCACTT[C/T]GGAGAGAGAAATATG	54476
rs565218499	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5734894	GGCATGGTGGCTCAC[A/G]TCTCCCAGCACTTTG	54476
rs565247404	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675503	AAAAATTAGCTGAGT[A/G]TAGTGGTGCCCACTT	54476
rs565255206	snp	G/T	0.00279162	0.0372561	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672842	AGCTGGGGCTTTCTA[G/T]GACACAGGGACACAG	54476
rs565256130	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5758114	ATCTCCAAAGTCAGT[A/G]ATTTTCCAAAATGAA	54476
rs565266998	snp	G/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5701069	AGCACAGCAGTGCTG[G/T]GGACAGAGAGTGCAG	54476
rs565283857	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5639469	CCACACATGGCTCCA[C/T]ATTTTTTTTTTTGAG	54476
rs565291743	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5645036	TGGCCAGGGTCATCT[C/T]GAACTCCTGATCTCG	54476
rs565302232	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5659352	CTAGTCAGAGGATGC[C/G]ACATTTAAGCTGAGT	54476
rs565329636	snp	A/C	0	0	intron-variant	RNF216	GRCh38.p7	7:5766083	GACGCTAGGGGTTCA[A/C]GACCAGCCTGGGCAA	54476
rs565365410	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5743023	ATCCCAGCATTCAGG[G/T]AGGCCAAGGCAGGCG	54476
rs565366771	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5748952	TCTATATATGCGTTA[C/T]GTGTGTGTGGTATTT	54476
rs565387115	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5772523	GCGATTCAATCCTTT[A/C]CTTCCTCTCTGAGAA	54476
rs565416801	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5654822	GTTCCCTCACCTACA[A/T]CCCATTCAGTAAACA	54476
rs565441684	in-del	-/G			intron-variant	RNF216	GRCh38.p7	7:5746148	GGAGCTGCAAGTGTC[-/G]GAAGTCCTTCTCAGG	54476
rs565444913	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5762063	TCATTATAGCAAATA[C/T]GTAATAAAAGCAATT	54476
rs565475492	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5691065	ACACAGCCGTGCAAA[C/G]AACTCTGTTCTCACG	54476
rs565494881	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5769290	GCCCAGCTAATTTTT[C/G]TATTTTTAGTAGAGA	54476
rs565495484	snp	A/C	0.00597247	0.0543191	intron-variant	RNF216	GRCh38.p7	7:5623682	CCAGTGATGCTCCCA[A/C]CTCTGCCTCCTGAGG	54476
rs565499988	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5746611	AAGTGATTGGCTAGG[C/T]AGGACATCTTGGAGC	54476
rs565504847	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5765097	AAAGTAAGGATGGGA[C/T]AAAACAATTTTTACA	54476
rs565547032	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5692572	GCTGCAAGCAGAGCC[C/T]GTGCAGAAGGCGAGC	54476
rs565552817	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5696146	GGGGAAACACACTGA[C/G]ATCCACAGTCCATGT	54476
rs565568780	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5723902	CTAAGTGTGAGTCAT[A/G]AACATTAAACTACTA	54476
rs565570652	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5729313	ATTTATCTTCACCCT[A/C]ATAAATTCCTTAGCA	54476
rs565586400	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5740883	TGAAGTCCACGCATA[C/G]CAACAACTTTTTTTT	54476
rs565592881	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668835	TGGGCGTTCTAGTCA[C/T]GGTGTATCTTCCCCA	54476
rs565610388	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5655181	GACCTGGCCAGGCTG[G/T]AGCCAGGTGCATGTG	54476
rs565625267	snp	G/T	3.29457e-05	0.00405854	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741282	AACGACCTGGTTTGT[G/T]ATTTCACGGGGCTGT	54476
rs565629635	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5658199	AATAAAGTGCTTCTC[C/T]TACTGGGATCTACGT	54476
rs565632287	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5750450	CTTTGGTAGAAATGG[A/G]AGTGACTTAGAGAGG	54476
rs565655662	snp	A/G	0.00835141	0.0640778	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669075	TCAACGCAGGCAGGT[A/G]GCTACAGATGGCCCC	54476
rs565658533	snp	A/G			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620152	TCTATTTTTACTACC[A/G]GAAGGTAAAGAAAAA	54476
rs565701064	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5652708	GGCTAGGTGGCTGAC[A/G]CCTGTAGTACCAGCA	54476
rs565712762	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679388	AGGGCAAGCTGTGGT[C/T]CGGCCAGCCTCACAA	54476
rs565731176	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5709383	ACAAATTCCCCAGCC[C/T]TTGATGCAACTGGTT	54476
rs565733024	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5641436	AGGAAAAAAATATGG[A/C]CATTAAGCATTTATT	54476
rs565746925	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5637679	GAGCTGGGAACACAG[A/G]TGTGCACGCACCACC	54476
rs565761517	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5708765	TTGGCCTCAGCAGCT[A/C]CAAGGCATCTAGAGT	54476
rs565775622	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673903	TCTTGCTCTATCGCC[C/T]AGGCTGGTGTGCACT	54476
rs565793413	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736894	CCCGGCAGCCGCCCC[C/G]TCCGGGAAGTGAGGA	54476
rs565795308	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5661098	GTATGCACCACCATG[C/T]CCGGCTAATTTTTGT	54476
rs565841727	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5637079	TGTGGAGCTCTTCAT[A/T]GCTCCAGCTGAAAAA	54476
rs565843011	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5771342	ACAATCTTAGAGGTG[C/G]AAAAGATACCCTAAA	54476
rs565845413	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673297	GCTTACGGTAATTAG[C/T]GTGGCCCTGTCAGTG	54476
rs565849577	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5775621	ACACCTGTAATCCCA[A/G]AACTTTGAGAGGCCG	54476
rs565858902	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5745966	CATTGCCTGATGCTA[A/G]ACTCACAATAAAGAC	54476
rs565899487	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5631658	CTCAGGGATTTGGTT[C/T]TCATCAACATAAAAA	54476
rs565913289	snp	C/G	0.00119737	0.0244387	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621552	ACCTTGGGTGGGCCA[C/G]GCCCTGCTTCAGGAG	54476
rs565934800	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5770994	TGTATTGTTAGTAGA[C/G]ACAGGGTTTCACCAT	54476
rs565951180	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736469	CGATCTCGGCTCGCT[A/G]CAACCTCCACCTCCC	54476
rs565958052	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5707514	TATATTAATTCTAAC[A/T]AGTTTTTTTGTGGAA	54476
rs565970214	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5728151	TACTAACATCTTCCA[C/T]GACCCCTTTCACCAA	54476
rs565971031	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5756066	GAGCGGGACAGGTGG[A/G]GGTAATCGGATCATG	54476
rs565971977	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676209	GAGAGATAGGGTTTT[C/G]CCATGTTGGTCAGGC	54476
rs565973511	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5731092	AATTGGGTGTTAATG[C/T]AATGAAGTCACTGAA	54476
rs565975383	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5727586	GAAATAAAAAGATCA[G/T]CCAGGTGTGGTGGCG	54476
rs565983811	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5648010	CACCCAGACACTGCA[C/T]AGCTCTGGGTGTTTT	54476
rs565983899	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5719464	AAACGGGGTCATTTG[A/G]CTGTGCCCAAAAGCA	54476
rs565987654	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5726300	AAACTGTCCAAGCTG[C/T]CCTTGAATAAGTACA	54476
rs565989295	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5687293	CTCAGCTACTTGGGA[A/G]GCTGAGGAGGGAGAA	54476
rs566017402	in-del	-/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5771221	TATGGGGTGGGAGTA[-/G]GGGGTAACAACCCCT	54476
rs566027883	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5632667	CTGTAATTCCAGCTA[C/T]TTGGGAGGCTGAGGC	54476
rs566032474	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5722804	AGGAGGGCACATCAT[C/G]TAAGGTTAGGAGTTC	54476
rs566045034	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5717735	GACTGCCAGGATGCA[C/T]GGTTAAATGAAAAAT	54476
rs566068856	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5689939	CTGTCTCAAACAAAA[A/C]AAAAAAAAGAACAGA	54476
rs566073857	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5626731	GCAGGAGGGCCGTGG[A/G]CCTACACCTCTTAGC	54476
rs566096568	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5711152	TAAAAACTCTAAGTG[C/G]CTTCTAAATAGCTGA	54476
rs566124889	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5770606	ACAACCTTTATCAGG[G/T]TTTAAGAATAGATAT	54476
rs566129931	snp	A/T	0.00199481	0.0315187	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678919	GGGAGCATGGCTGGT[A/T]TATCAGTTGCTCTCC	54476
rs566131006	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5626739	GCCGTGGGCCTACAC[A/C]TCTTAGCTAAGTGAG	54476
rs566144494	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5685440	GAGGATTGTTGGGAG[A/G]GCAGGGCTATAGAAA	54476
rs566149043	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5779102	CAGGTATGAGAATGA[A/T]TTATGTCTCTAAAGA	54476
rs566149776	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5735975	GCGCATGCCTGTAAT[A/C]CCAGCTACTTGGGAG	54476
rs566164620	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5686128	TTCGGGAGGCTGAGG[C/G]AGGAGAATCGCTTGA	54476
rs566166161	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5701009	CCCTGAGATTCTAAA[A/C]CTTCTGAGTAGGAGT	54476
rs566177970	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674694	CTAGTCCAAAAAGAG[A/C/G]TGACACTCACTCATT	54476
rs566225865	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5700251	CACACACCACAAGCC[A/G]CACACGTGCACTCAC	54476
rs566235528	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5735649	ACAAAGAGGTGGACT[C/T]AGAGACATGGAGATT	54476
rs566241424	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677999	GGGGGTAACCAGATT[C/T]TGCGACTGTTCTTGG	54476
rs566246660	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5657192	GGGGAGAGAAGTCAC[C/T]GACATGCCACAGGGC	54476
rs566252829	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5755005	TGCACTCCAGCCTGG[A/G]TGCTAGAGCAAGACC	54476
rs566258907	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5656693	ATACATTAAGGTGTT[C/T]TGGCTGTTCATGAGG	54476
rs566280134	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5695014	TTCTGTGGCTCAACT[G/T]TAACTGAGCCAAAAA	54476
rs566287646	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5694632	CTCCAAGCCAAAGGA[A/T]GAGGCCCACTTGTGG	54476
rs566289476	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5661866	TCCAATTAATTTGGT[A/C]GAGGTCACAGAGCTT	54476
rs566290427	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5764253	CATTCAAACCAGCAA[C/T]GGTGTGGTGAAACTA	54476
rs566314362	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5624627	CTGGCCTTGGCTCCT[A/G]GGCCAGGCCTCGGGG	54476
rs566316500	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5716502	AATGATTTTTAACAG[C/G]AACATCTATTATCTT	54476
rs566319382	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5688246	AAAGCAGAGTAGAAA[A/G]CTGTTAAAATGTAAC	54476
rs566326848	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5773756	TATTTTTAGTAGAGA[A/C]GTGGTTTTGTCATGT	54476
rs566327564	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5693883	GGAGATGCTATTTGC[C/T]TAAGAAATCAGCCTT	54476
rs566346270	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5765163	ACTCAAAGAGCTATT[A/T]AAAAAATGAACTTCA	54476
rs566348207	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5759951	GAGTCATTTTTGTAA[A/G]GTCAAATGTAATTTA	54476
rs566351458	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	RNF216	GRCh38.p7	7:5783390	CCACCTCGGCCTACC[A/G]AAGTGCTGGAATTAC	54476
rs566385220	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5760478	TCGAGATTACGCCAT[C/T]GCACTCTGGCCTGGG	54476
rs566388557	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678240	CTCCTCACCAGACCA[A/G]TAAGAAAACCAGTCT	54476
rs566413435	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5769398	TGGGATTACAGGCGT[A/G]AGCCACCGCGCCTGG	54476
rs566432212	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750323	GTTTCCTAGCAGAGA[C/T]ATTTTTTAAAGACCA	54476
rs566436476	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5744814	CCCATCTCTACTAAA[A/G]CTACAAAATTAGCTG	54476
rs566436888	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5641002	GTAGCTGATAATTAG[C/T]TTCTCAAATTTTTTC	54476
rs566454191	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5694318	GCTTGCTTCCGCCAC[A/T]GCTACTCAATGATAT	54476
rs566471659	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5636485	TTCCCTCCAAAACCA[C/T]GATGGGACAACTCCC	54476
rs566474245	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5778767	TATTATTTTTGAGAC[A/G]GAGTCTCGCTCTGTC	54476
rs566512019	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656206	CCCAGGAGGTGGAGG[C/T]TGCATTGAGCTGAGA	54476
rs566518150	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5745267	GATGCTGAAATTGAA[C/T]GTAACAGAATCCTAC	54476
rs566528348	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672638	CTTGCTGGTACCCGA[C/T]GATAAAGACTCATCG	54476
rs566528399	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666866	GTCACCCAGGCTGGG[A/G]TGCAGTCAGTGGTGC	54476
rs566545594	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5739767	GCACTTTGGGAGGTC[A/G]AGGCAGGCGGATCAC	54476
rs566551154	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5692943	TCTATCCTTCCAAAT[A/G]GATTTTATGTCTGTG	54476
rs566555116	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666114	GAGCTTGCAGTGAGT[G/T]GAGATCACGCCACTG	54476
rs566567644	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620798	TTGTCCTGCCTGGGG[A/C]TCTTGCTGGAGCCAC	54476
rs566584899	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667331	ACAAACAAAAAAGTT[C/T]AAAAGCCATTAATTT	54476
rs566597939	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5763689	AATCCTCCTGCCTCA[G/T]CCTCAGAGTAGCTGG	54476
rs566605667	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5769934	CAGGAGGCTGAGACA[C/G]AGGAATCACTTGAAC	54476
rs566639798	snp	A/C	0.00874735	0.0655527	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620432	TGGCTGGTCTGAAGA[A/C]CCCCAGTGCTTCTCT	54476
rs566645419	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5715661	AGCTATAACTAAAGC[A/G]GCAACCTCAAGTAAT	54476
rs566659230	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5693343	GCTGACCCCTGGTAT[C/G]GATGTTTACAGAAAA	54476
rs566675967	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5779569	TTCTGGCAGAGCACG[A/G]TGGCTAAAGCCTGTA	54476
rs566690424	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754415	GCTCCTCCCACCTCG[A/G]CCTCCCAAGAAGTCA	54476
rs566703257	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675668	AACAAACAAACGAAC[A/C]AAGGAGCAAGGTCAT	54476
rs566703393	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5725641	GATCCCTTGAGGTCA[A/G]GAGTTCGACACCAGT	54476
rs566723509	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5683520	AAGGCCACAGGCACA[C/T]AGCATCATGACTTAA	54476
rs566724319	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5734044	CAAAAAGAAAGTATT[C/T]TAAAAGCTTAGGAGG	54476
rs566751941	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5721522	AATAGCGCTGCTTAT[A/G]GCCATTTGTTGGTGA	54476
rs566755353	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5624521	ACAAGCGCTCGGCAT[A/G]GCAGCCTGTCTGCAG	54476
rs566768270	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5743215	TGCAGTGAGCCAAGA[C/T]GGTACCACAGCACTC	54476
rs566774409	in-del	-/CTG	0.00795532	0.062565	intron-variant	RNF216	GRCh38.p7	7:5686283	CTCTCAAGAACACCA[-/CTG]CTGCCACGTGGTTTC	54476
rs566777598	snp	A/G	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5660332	GAGTCTCGCTTTGTC[A/G]CCAGGCTAGAGTGCA	54476
rs566797602	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5749815	GGATTTGTGTAACTG[C/T]TAACCAAGATCAAAC	54476
rs566807386	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5743800	TCCCTGAGGACTATG[C/G]CACTGAAGTAAGGGC	54476
rs566868711	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768288	AGATCTTGTCGCTAT[G/T]AGGGGGAAAAAAAAA	54476
rs566880381	snp	C/T	0.00835141	0.0640778	intron-variant	RNF216	GRCh38.p7	7:5698870	AACATTTTCCTGTTA[C/T]GTTGCACATTTTCTC	54476
rs566913982	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5729791	TGTCTGGAGCCGACA[C/G]ACTAGTTTTACTACT	54476
rs566919136	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5659969	TTTTTTTTTTTTTTT[C/T]TTAGAGACAAGGTCT	54476
rs566925920	snp	A/C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5730156	CACTCTGGGTAATGA[A/C/T]CTGCATGCTGAAGTA	54476
rs566929090	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666428	GAGGGAGAGAGTCTG[A/G]TGCTATCTGGGGGAA	54476
rs566939047	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5682506	CCTGCTTCCTGGGTT[C/T]AAGCGATTCTCCTGC	54476
rs566946733	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5660700	CTCCCACCTCAGCCT[C/T]CCAAGTAGCTGGGAC	54476
rs566956951	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5655859	ACGAAGAAACGCTCT[G/T]GAATGGTTTTTTTTT	54476
rs566989195	snp	A/G	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5730453	ATTAAAGATATGGAG[A/G]ATTCGTTCAATTCTT	54476
rs566996958	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5624963	GATGCCTGCTTCATG[A/T]GTGGCGCTTACCTTA	54476
rs566997848	snp	A/G/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5650103	AATGTGTCATCTCTA[A/G/T]GAAGTTCTGGTGGTC	54476
rs567008628	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5772637	TCTACAAAGAGTTAA[C/T]AGTCAAATAATATCA	54476
rs567011360	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5742685	ACTCCAACTTCTGCC[C/T]CCCAGGTTCAAGCAA	54476
rs567034450	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5650468	TAGTAGTCCAGATGC[C/T]TTATCACAGGGCTGC	54476
rs567042432	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5709584	ACAAGAAGCTACATG[A/G]CTACCTTCAAGTTCA	54476
rs567065393	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665589	AAGTTACAAGGCACC[A/G]AGACACCAGCTTGAC	54476
rs567098226	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5704765	TTCCTCTGGTGGTCA[C/T]TGAGCCAGCTCCACC	54476
rs567116429	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672494	AGCATCAAGACAATT[C/T]GGAGTTTAACCCACT	54476
rs567119342	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680853	CCTCCTTTCTCTTTA[C/T]CCCCACTCATTCCAG	54476
rs567126028	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5733269	GCTTTTTGGATTTCA[C/T]GAGAATTTTAATGTG	54476
rs567130687	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5732911	GTTGCTGCCTTCATC[C/T]AACTGAAGCTGACCA	54476
rs567154241	snp	C/T	0.00438332	0.0466095	intron-variant	RNF216	GRCh38.p7	7:5687051	TAATTGGATTCATCA[C/T]CACAGTCAAGTGAAT	54476
rs567156605	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5711046	TTCTTTACTCTCCCC[A/G]AGGCAAAGATATTGC	54476
rs567165927	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5705116	TTTTGCTGCTCATTT[C/T]AGACTCCAAAATCTT	54476
rs567179233	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5728707	TATTTTAACCACTAC[A/G]ATAACTCCACGTTTG	54476
rs567182867	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5724037	AACAAGAAACTGAAT[A/C]AAATGAAATGAAGTT	54476
rs567183764	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678632	AGGAGGCCGGCACTC[A/G]TAGTGACAAATATCA	54476
rs567187042	snp	A/C	1.65756e-05	0.00287881	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5752984	ATTGATCCACTCTAC[A/C]GGAAAGCAGAGAACA	54476
rs567194788	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5772944	CCACCATGTCTGGCT[A/G]ATTTTTGTATTTTTT	54476
rs567217397	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681525	GTTCTCAAGCCTCTA[C/G]GGCTAGGCAGGACCT	54476
rs567220570	snp	A/C	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5710377	AACTTAAAAACAAAA[A/C]CAAAAACAAAAAACG	54476
rs567224186	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5654468	AAGGCAGGCAAATCA[C/T]TTGAGGTCAGAAGTT	54476
rs567227518	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712925	TAGAAAAATAAAAAG[C/T]GTCAGTGGTTAAAAA	54476
rs567229465	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5623780	GGGTCTACTTTTCTT[A/T]AGCCAGGTGTGGCTT	54476
rs567231951	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5777823	AGGAAAGGTTTTAAA[C/T]CAAAAATTAAACTCA	54476
rs567242615	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5729116	GGATGGTCGTGTGAC[A/C]TGTCCCAAGTTGGAA	54476
rs567267592	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5692307	GCTAACTGTTACACA[C/T]ACTAGGAAAGTAACA	54476
rs567278820	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5624472	GGGCTGGGTCTGAGT[A/G]GGCACAGCCTGAAAA	54476
rs567285886	snp	C/G	0.000399281	0.0141238	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619647	AATGCCATGGCCTCT[C/G]AGCCCAGGCACTTCC	54476
rs567310893	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5703007	TAAGGGAGCGTCCTT[C/G]TGCGGCCTGAACCTG	54476
rs567336669	snp	A/G	0.0185938	0.0946107	intron-variant	RNF216	GRCh38.p7	7:5687409	CAAAAAAAAAAAAAA[A/G]AAAAAGAAAAAGAAA	54476
rs567341095	snp	C/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781384	CCCCTTGGCCCGATC[C/G]CGCCCGGGCCTCGGC	54476
rs567361265	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782123	TTGGGAGGCCAAGGC[A/G]GGTGGATCACTTGAG	54476
rs567379073	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753382	TTATCATTCAAAAAA[C/T]AGTAAAATTTTAATT	54476
rs567397869	snp	G/T	0.00119737	0.0244387	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782616	GCACATTGGGAGGCC[G/T]AGGCAGGCAGATCAC	54476
rs567404436	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713846	CTCATTTAGCTTTCA[A/G]AACAATGCTATGATT	54476
rs567437719	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5658978	TTAGTGAGCTTGAGA[C/T]CAAAGACAGAAAGAT	54476
rs567447605	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5633055	TGCGATCTCTGCTCA[C/T]TGCAACCTCCGCCTC	54476
rs567452970	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5766921	ATAATGATAATGTCC[C/T]TGGGTCCTGTTCCAG	54476
rs567453090	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669476	CCTCAAGTGAAAGAT[C/T]ATATTGACAGATTTA	54476
rs567492115	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5623339	ACTGCAAGAAACCAA[A/G]AACAAATCTGTACTT	54476
rs567492419	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5697056	TTTTGTTCTGCATTG[C/G]AAAGCCCTCAACAGG	54476
rs567501843	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643539	CTGTAGTTATCTGTG[C/G]TCACCACCAGCCAGT	54476
rs567512032	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664794	AGGACACACAAAATT[C/T]TTTTTTTTCTTTTTT	54476
rs567522160	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5762261	GGCGTGGTGGCTCAC[A/C]CCTGTAATCCCAGCT	54476
rs567568407	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5635680	GCCTGGGAATACTCC[A/G]AGGACAAATGACCCG	54476
rs567569078	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5723722	TCCTGCATGACCATA[A/G]AAAGGACAGAGGAGG	54476
rs567572277	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5774826	TGCAATGGTGCAATC[G/T]CAGTTCACTGCAACA	54476
rs567575333	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5659554	TTTGGAAAGCTAGGC[C/T]GACCAGGTGGGAAAT	54476
rs567577268	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5762688	CAGAGCGAGACTCTG[C/T]CTCGAAAACAAACAA	54476
rs567589083	snp	C/T	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5629192	AGAGCAAGACTCTGT[C/T]TCAAAAAAAAAAAAA	54476
rs567606505	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5650373	AGTGCCAGGAACCGA[C/T]AGGACAATCAGAATG	54476
rs567608335	snp	C/G	0.00835141	0.0640778	intron-variant	RNF216	GRCh38.p7	7:5776566	GGCCACTGCACTCTA[C/G]CCTGGGCGACAGAGC	54476
rs567615164	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5717835	TCGCCCAGGCTGGAG[C/G/T]GCAGTGGTGCAATCT	54476
rs567627307	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5718402	CAAACAAACAAAATG[A/C]GAGAAAGGGACAGCA	54476
rs567630421	in-del	-/AAAT	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5723655	CGTCTCAAAAAAAAA[-/AAAT]AAATAAATAAATAAA	54476
rs567667207	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5776131	CCATATCCATATGTG[A/C]AAGCTGTGGATATGG	54476
rs567695051	snp	A/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5770965	GGCATGCACCACCAC[A/G]CCCGGCTAATTTTTG	54476
rs567695457	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5771855	ATTTGAATTAACAAC[A/G]GCTGAGTACCCCGAG	54476
rs567698474	snp	C/T	4.94173e-05	0.00497053	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741518	GGTTGACAATGTCAT[C/T]TGCTGCTTGGTTATG	54476
rs567705945	snp	C/T	0.00318978	0.0398085	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674766	TCTAGGAGGCCGAGG[C/T]TGGCAGATCACCTGA	54476
rs567715453	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674978	CTCCAGCCTGGGCGA[C/G]AGAGAGAGACTCTGT	54476
rs567715574	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5771534	GGGTGCAGTGGCTCA[C/T]GCCTGTAATCCCTGC	54476
rs567729834	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736845	GCCCCTCCGCCCCGC[A/T]GCCACCCCATCTGAG	54476
rs567734713	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622206	CCTGACTTTCCAGAG[A/G]CCGAGGATGAGAAAG	54476
rs567735911	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5708187	GAAAATGTTCCATGC[A/G]CAACAGAGGAGAAAA	54476
rs567737978	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643926	CATATGCCTCTGATA[C/T]TTCATAGGAATGGAA	54476
rs567739443	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5695196	TGGGTTATATGACCT[C/T]CTGGGTCCGGCTTAT	54476
rs567763950	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663672	TTGGGAGGCTGAGGC[A/G]GGCAGGTCACGAGGT	54476
rs567764113	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5648641	GCTGAGGCAGGAGAA[C/T]GGTGTGAACCTGGGA	54476
rs567780121	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5632535	GATGTGTCAGGCCAG[A/G]GTAGAAGTTAGCCCT	54476
rs567788982	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5765563	TGAGCCCAGGAGTTC[C/G]ACACTGCAGTGTGCC	54476
rs567795463	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5702452	TACCTTTCCCTATTT[C/T]GGGTTGTCAGCTCTC	54476
rs567798110	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5756784	AACCCAAGACCACCA[C/T]ACCCAGCTAAATTTT	54476
rs567830976	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5686010	GACGGATCATCTGAG[C/G]TGAGGAGTTCGAGAC	54476
rs567848156	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5695560	CTGCAGAGCAGAAGA[C/T]ACCGCAGCTATAGAC	54476
rs567859599	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5723244	CTGTAATTATCAATG[C/T]TACAAATTAAAAAAA	54476
rs567863138	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622819	CATCCACACTCCTAC[C/T]CCAAACGGGCTTTGT	54476
rs567878802	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5649108	GACGGCCGGGCGGGC[A/G]CGGTGGCTCACGCCT	54476
rs567894510	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678347	ACCTGCGTTTCATAA[A/G]CAGGATCAGAAGAAT	54476
rs567896045	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5653372	GAGGTGGGCGGATCA[C/T]GAGGTCATGAGGTCA	54476
rs567897613	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5755065	CAAGGGAGGGAGGGA[C/G]GGAACTGAAGGAAAG	54476
rs567918073	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679654	AATCAAAACCACTGA[A/T]ATCGAGAGAATAGCC	54476
rs567921961	snp	C/G	0.00795532	0.062565	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678835	GAAGACATGAGAGCT[C/G]GACTGGATAAATTAA	54476
rs567931221	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5740818	CCATTTTCATGTCTT[C/G]AGAGTGTCTCTTCTA	54476
rs567955180	in-del	-/TCCAG			intron-variant	RNF216	GRCh38.p7	7:5759580	GTTATCAGTAAGGCT[-/TCCAG]TCAACAGTAGGCTAT	54476
rs567962504	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643080	ATGGGTATGGAGGGA[A/G]AAAAAAAGGCTCTCC	54476
rs567972528	snp	A/G			downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619958	AGTCGGGGAGGTGAG[A/G]ATGCTGGTTTAGACC	54476
rs567979199	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780795	TGCTACCCAGGCCCT[C/T]AGGGATTTACAGAGC	54476
rs567984350	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5701557	AAAAGCTCTACGAGG[A/T]AGGTGCAACCGTTCT	54476
rs567984791	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673167	ACCTGCGGGCAGTAC[C/T]GCACTGGTCACCAGC	54476
rs568007529	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5701132	TCCCCCAGCACGTGG[C/T]TCTCCCCAGGTTGCA	54476
rs568010810	in-del	-/AAAAAAAAAAAA			intron-variant	RNF216	GRCh38.p7	7:5738106	AAAAAAAAAAAAAAA[-/AAAAAAAAAAAA]TTACAATTATTTCAC	54476
rs568016405	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5765833	TGGCAGTATGTGCCT[C/G]TAATCCCAGCTACTC	54476
rs568028893	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5632216	GGCAGGAGGGGCTGC[C/T]GGCTGCATCTTTACT	54476
rs568028996	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5736093	GTGAGACTCCGTCTC[A/C]AAAATAAATAAATAG	54476
rs568033602	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668145	TTTATATAGCAGGCA[C/G/T]AGAAAAGCGGCTGCC	54476
rs568053290	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5770715	TTACAGTAGGAGATA[C/T]TGTATTACTATTAAG	54476
rs568068274	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5632597	GCCTGGCCAACATGG[C/G]GAAACCCCATCTCTA	54476
rs568081076	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5656568	CGCCCTCTCAGGGGG[A/G]AAGGAGCATGCATGC	54476
rs568082067	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5651603	AAGGCTAGATTGTTA[C/T]GAGAGAAGAGAAAGA	54476
rs568090410	in-del	-/TATACATACTCGTC	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5758074	ATGATGGGTGCAGAG[-/TATACATACTCGTC]TAACAAAATATATCT	54476
rs568096434	snp	A/T	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662640	AGAGCCTTCCATCAG[A/T]GCCGCTGAGAGCCTT	54476
rs568101686	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5627327	AGGACCGTGCTGGAC[A/G]CTGCAGACACAGTGA	54476
rs568106283	snp	C/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767430	GGGACAAAATTCCAG[C/G]AAGGAAGAATCCACT	54476
rs568107111	snp	A/G	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5731660	GAAGCTTCTTTGCTC[A/G]GAGGGTAATGGGGAC	54476
rs568116049	snp	A/C	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5647644	TTTCCTATACTTAAT[A/C]TCTCCCACTCCTGGT	54476
rs568119583	snp	C/T	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5731994	TGCATTTCCCTTTGC[C/T]GTTACTTCAGGAGTC	54476
rs568120285	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5745493	ATTAGACACGTGAAA[A/G]AAGCATAAAAATTGG	54476
rs568123694	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5657336	ACTTTGGGAGGTGGA[A/G]GCAGGTGGATCACCT	54476
rs568150873	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5651610	GATTGTTATGAGAGA[A/G]GAGAAAGAGATTTCA	54476
rs568161109	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5684329	AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT	54476
rs568180418	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5680121	ACGTTCTTCACACAA[C/G]GGACATCTCCCCCAC	54476
rs568186015	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621759	TCATCTGTCAATGGG[C/T]CAGAGTGATGCCTCA	54476
rs568195434	snp	A/G	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5726027	CACACCTGTAATCCT[A/G]GCACTGTGGGAGGAT	54476
rs568209220	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5770443	TCCAGCCTGGGCAAC[A/G]AGAGCAAAACTCCGT	54476
rs568236830	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5717235	GCGTGCACCTGTAAT[C/T]CCAGCTACTTGGGAG	54476
rs568236939	snp	C/T	0.000330365	0.0128481	intron-variant, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711712	GCCATGAGGGCAGCC[C/T]ATAATACCATAATTC	54476
rs568237381	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750399	TGTGCTTTCAAATAT[A/G]TGGTTAGTCAGGCAA	54476
rs568260364	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5779820	GGAAATACAGCCAGA[C/T]TCCGCCTCAAAAAAA	54476
rs568280606	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5635804	TGTATTAACATCTAT[A/G]AATGTTAGGCTCAGT	54476
rs568287242	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5745844	GATGTTGCAGTGAGC[C/T]GAGATCAGGCCACTG	54476
rs568296860	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5774996	GTGATCCACCCCCCC[A/G]ACACTCACCAAAGTG	54476
rs568304105	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5775581	CCAGCAAAAAGTGGG[C/G]AAAGCAGGCCAGGTG	54476
rs568320309	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5735336	AAATACACAAGAAAA[C/T]TAGGCACCATGGGAG	54476
rs568336459	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5770337	GTGGTGGCACATGCC[C/T]GTAATCCCAGCTACT	54476
rs568342313	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5661719	GAGGCATGAGAATCG[C/T]TCGAACCTGGGAGGC	54476
rs568343819	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712175	GGGGGTGCCAAGATA[A/T]GTAGACAGAAGTTTG	54476
rs568350145	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5636664	CGGTCTCCTGGTGAG[A/G]ATCAAGGAAACGGGG	54476
rs568356385	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5688925	AAGTCTGAACTCAAA[C/T]GTTGACTGAATGAGA	54476
rs568363234	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767497	ACCCCCCACCAAGTT[A/G]TTAACCTATGCCACA	54476
rs568394466	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5728453	GTGGTGAGCACCTAC[-/A]GTCCCAGCTACTCAG	54476
rs568394908	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5637045	CTCTGCCCTTTGTCT[C/G]TAGAGATGAAATACT	54476
rs568405700	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5735563	GTTAAAAGGAGATTA[C/T]ACTCTACTGAAGAGA	54476
rs568436191	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5731046	CAATGAACATACTGA[C/T]TAAGGCAAACTCCTC	54476
rs568437125	in-del	-/TT	0.00993419	0.0697739	intron-variant	RNF216	GRCh38.p7	7:5774471	TTAAAAAATAAAAAC[-/TT]TTTTTAAAAACTAAA	54476
rs568458537	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5694572	AAGGTAAGTTTAAAC[A/G]ACAAAACAAATCTCA	54476
rs568474758	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5726206	CACTTGAGCCTGAGA[A/G]GCAGGGTTGCAGTGA	54476
rs568478479	snp	C/T	0.00914312	0.0669923	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621323	GGGATTATAGGCATG[C/T]GCCACCTTGTCCGGC	54476
rs568480416	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5693664	GAACTGTAGGTCTTT[C/T]GATAAGAGGAAATTC	54476
rs568499054	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5697710	AGAATCTTTACAAGC[A/C]ATTTGAGGTGCTTAG	54476
rs568542940	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5719142	CCCCAACAATTTGGG[A/C]GGCTGAGTTGGGAGG	54476
rs568549687	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5708414	GCACTGATGTCGGGT[A/G]CATATACAGATGGTC	54476
rs568554807	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5644849	TTTTTTTTTGAAACG[C/G]AGTCTTGCTCTGTTG	54476
rs568557412	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5691649	AGCACAACTTCTTAG[C/T]GTCCTCAATCAAGTG	54476
rs568597676	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5716032	AGGAGTGAGCCACTG[C/T]ATCCAGCCCCATTCT	54476
rs568619648	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5717315	CCGAAATCGCACCAT[C/T]GCACTCTAGCCCGGG	54476
rs568630800	snp	C/T			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622468	TGCCCTTGGCCCAAC[C/T]GTGGGCCCCTCCAGG	54476
rs568633841	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5764035	CTTCTACTAAAAATA[C/G]AAGAAATTATCCAGA	54476
rs568643315	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5630974	ACCTGACTGGGGGCC[G/T]GAGAACACTGCTGTC	54476
rs568652561	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671930	GGGCCTCACAAGAAA[C/T]GAAATCTGCTGACAA	54476
rs568656584	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5769263	GCTGGGACTACAGGC[A/G]TGCGCCACCACGCCC	54476
rs568667298	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5692883	ACTCCTCCCTTAACC[C/T]TTGGTGAGCATCCTC	54476
rs568670223	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5759316	TTGGGCATTTCTTTA[C/T]AGCCAGTGGAGAACG	54476
rs568684526	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5661834	AAAAAGGTAAGAGAA[A/G]AAGAAGGCTCAGAGG	54476
rs568685960	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666711	TCTCACAGCCTGGAA[A/G]GGGCAGGAGGGGAGG	54476
rs568691730	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5643535	ACTCCTGTAGTTATC[C/T]GTGCTCACCACCAGC	54476
rs568699952	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5661313	AGCATAGCTCATGGC[A/G]GTCTCCTCAGTAGCC	54476
rs568729191	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5693276	GGGATAGATACCATA[C/T]GGTCCGCAAAGCCTG	54476
rs568735292	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5776820	GCACAAGAATGGCTT[C/G]AACCTGGGAGGAGGA	54476
rs568735293	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619996	TTGGACGAATCTGTC[A/G]GCGGCCCCTGTAACT	54476
rs568744152	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5769807	TTTGGGAGGCCAAGA[C/T]AGACGGATCACTTGA	54476
rs568746671	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5764558	GAGGTTGAGGCGAGA[A/G]AATCGCTTGAACCCG	54476
rs568775168	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5625442	AATGATCAGTTTGGA[C/T]TTTTTCATGCCGATC	54476
rs568789546	snp	C/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5646045	ATGTGTCCTCAGAGA[C/T]GGTTTCTATCAACTA	54476
rs568800277	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5744130	AAGTAACAGCATGTT[C/T]AGGGAAATCAAAGAC	54476
rs568803053	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5694099	GGAAATTATACCACT[A/T]AGCTCTTTGATAGAT	54476
rs568809124	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5720554	GCACAGGGGGAAGCA[C/T]TCCTAACTTTCATGT	54476
rs568825527	snp	G/T	0.00478085	0.0486577	intron-variant	RNF216	GRCh38.p7	7:5749208	CAGGCTAGAGTGCAG[G/T]GGCGTGATCTTGGCT	54476
rs568830177	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5682522	AAGCGATTCTCCTGC[C/T]TCAGCCACCCGAGTA	54476
rs568840958	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5739055	TGGGTGCCACTGGCT[G/T]GGGAAGGGGATGGGG	54476
rs568841322	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5710457	ATAAGCACTTTCACT[A/G]GCAGACCTTCTTTGA	54476
rs568851967	in-del	-/T	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5698092	ACTTTTATGAGGCTA[-/T]TGGGGATTTCATCTG	54476
rs568885364	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5778737	CAGCACCTCAGTTTC[C/T]TTTTTTAAAATTATT	54476
rs568898709	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5772571	CCTTCCTGGGAGAAA[C/T]CACTGTGCCTCAGAG	54476
rs568898806	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767599	CATGTATTGTTGAGA[A/G]GGATTTTTTTTTTTT	54476
rs568914110	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5749689	AATTATAATCCTAAA[A/G]TGCTGTGTGTTCAAA	54476
rs568925681	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5773092	GCCCCAGGTATTCCC[A/G]CTTTTAAAACTGACA	54476
rs568930985	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5697551	GGCTTTTTTATTCTT[G/T]TGTTTGTTTAAAGAG	54476
rs568973727	snp	C/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768230	CTGAAGCAGGAGGAT[C/G]ACTTGAGCCCAGGAG	54476
rs568978704	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5710982	AAAAGAAATAAAGTT[G/T]TGATCCATTAGTTTA	54476
rs569008812	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5762306	GGTGGATGGATCACC[C/T]AAGGTGAGGAGTTTG	54476
rs569021439	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5763633	TGGAGAGCAGCTACA[C/T]GATCACGGCTCACTA	54476
rs569049500	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5623913	TGTGGCCGCGTGGGT[G/T]AAGTCAGGTCTATAG	54476
rs569052840	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5650627	TTCTACAGGCTACCT[A/C]AATCCTTGGCTCATG	54476
rs569062824	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674220	TTTTTAGTAGAGACG[A/G]GGTTTCACCATGTTG	54476
rs569073089	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5645635	CTTGCTCTGTCCCCA[C/T]GCTGGTGTGCAGTGG	54476
rs569100493	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753646	TGGGTAACACAAACT[A/G]GTATTTTTTCCTGTC	54476
rs569116355	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675135	TTATTTTAAATAATG[A/G]CAGGGAACAATGTAG	54476
rs569140270	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670311	ACTGCTCCCCTGAGA[A/T]GACACATGCCTGACC	54476
rs569160918	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5629429	TATGATTGTGCCATT[C/G]TACTGGCACAACAGG	54476
rs569164275	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5688188	AACTGAAAGCATTTC[A/G]AAAATGATTAGTCTT	54476
rs569177964	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675638	AGAGCAAGACCCTCT[A/C]AAAACAAACAAACAA	54476
rs569188672	snp	A/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754001	CCCCATCTCAAATTT[A/T]AAAAAAAATGCATTA	54476
rs569199837	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5709926	TGCCTAGCTGAGTTT[C/T]AAAATTTTTTTTGTA	54476
rs569204422	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665006	TTTCACCACGTTGGC[C/G]AGGCTGGTCTTGAAC	54476
rs569205705	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5744047	GAAAATCAAAACAAG[A/G]GAAGTAACAGACAAC	54476
rs569242289	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5737725	GAAGAAACTCACCTG[C/G]AACCTTGACTGAGAA	54476
rs569247941	snp	A/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5772290	TGGGAAGACAGTAGT[A/T]GTAACAGCAGAATAG	54476
rs569253055	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5763287	TTGTCAAAACTCACT[G/T]AACTATATACTAAAA	54476
rs569275349	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5729737	ACCAGCCCTATAAGA[C/G]AGATGAGAAAACGGT	54476
rs569276462	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5738275	TCTGGCTCCCAGGCT[A/G]GAGTGCAGTAGCGTA	54476
rs569278388	snp	C/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5733492	AAGGAGAGAAAAACA[C/T]TGAATATACTCAATT	54476
rs569284174	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670758	CCTCTCATCTTTGTT[C/G]AGTTGTGTTTTCAGC	54476
rs569292049	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665520	ATTAGGTGACAAATT[A/G]GAATAGAAGCTTTAT	54476
rs569314591	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5704611	ATACTTTTCAAACAC[C/G]CAAGAGGAAGAAAAC	54476
rs569343283	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5658881	AATTGTACATCTGCC[A/G]CTCTCAATACTGAAG	54476
rs569348832	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5689363	ATATTTGTAGTATTA[-/A]AAAAAAAAAAAAAAA	54476
rs569364708	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5734004	ATTTAAAAAAATGTA[A/G]TTATTATCATGCCAC	54476
rs569366177	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782084	TGGCTGGGCACAGTG[A/G]CTCACGCCTGTAATC	54476
rs569379881	snp	A/C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5629909	CCTAGTCCCTCATAA[A/C/G]ATACTTCTTGGACTT	54476
rs569389704	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5650076	TAGAGAGAGAAATCC[C/T]TTGAATGTAGGAATG	54476
rs569393214	in-del	-/AAAACAAAACA	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5633589	CAAACAAAACAAAAC[-/AAAACAAAACA]AAAACAAGGAAATAA	54476
rs569393551	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5660191	TTTCTGGGCTCAAGC[A/G]ATCTGCCCACCATGG	54476
rs569401606	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5777196	GCGGATGCTCCAGCA[C/T]TGGCCACCTCTGCTG	54476
rs569406339	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5714065	TGGAGTGCAGTGGTG[C/T]GATCTCAGCTCACTA	54476
rs569429402	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5644067	CATTGTATGAATATA[C/T]CATATTAGTTTATTC	54476
rs569475289	snp	C/G	3.29468e-05	0.00405861	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741383	CAGCTGACTCTCCTA[C/G]ATTTGATAACAGCTC	54476
rs569484961	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5638013	AACCTGTAGTGGCTG[C/T]GCAGCAGCCCCCTTG	54476
rs569496684	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5709395	GCCTTTGATGCAACT[A/G]GTTTCTGGATTTCTC	54476
rs569503181	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754028	ATTAAGTGACCTAAA[A/G]GAAGAGAAGAAGAAA	54476
rs569518497	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736817	CCCGGCCGCCCCGTC[A/T]GAGAAGTGAGGAGCC	54476
rs569563251	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5644430	ATTTCTGTAATGACT[A/G]ATGACGTTCAGCATG	54476
rs569570789	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5691650	GCACAACTTCTTAGC[A/G]TCCTCAATCAAGTGA	54476
rs569579686	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5697773	GCTAGGAGCACAACA[C/G]GTTAGGTCAGAGTAG	54476
rs569582691	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5777600	AGTTGACCTAGACGC[A/T]GAGATCAGGTGACCA	54476
rs569587128	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5728600	GAAAAAGAAAAAGAA[A/G]AAGAAAAGGTGGAAG	54476
rs569588707	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5730086	TGAGATCTGGTTAAA[C/T]AGATGTATAGTATAC	54476
rs569590958	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5691114	TTAAGTTCCGACAGA[A/G]GCACACCCATTTCTC	54476
rs569600023	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5639215	CTCACTGCAGCCCCT[C/T]TGCTGCTTGGAATGT	54476
rs569624998	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5641498	TTTTGTGACATTAAA[A/C]AGTGAAAAGAGCCTA	54476
rs569635709	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5658349	ATAAGCACAAAGTTT[C/T]CATCTCATTAAATAA	54476
rs569641607	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5732851	GAAGTCACTCCTGCA[A/G]AGTAAGCCAGGCTAG	54476
rs569644595	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5654375	GACCCTTCTGGTGGG[A/C]TGTCGTAAAAAGCCT	54476
rs569649519	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5751769	ACCTACTGAATTTTA[C/T]GGAAGGAAGTGTTCC	54476
rs569662010	snp	A/G/T			intron-variant	RNF216	GRCh38.p7	7:5684532	CTTCTCCTGGGCCTG[A/G/T]CCCCATGCAGTTCGA	54476
rs569669249	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5649638	AAAAAAAAACACATC[A/G]CCAGATTCCTTTGGG	54476
rs569683904	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5686434	GAAAGTCAGAGTAAA[C/T]GATGTGCGGACAGTC	54476
rs569697115	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679220	CGGTGGCGGGGGGGC[A/G]GTGCACACAGCTAAC	54476
rs569727022	snp	C/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5762630	CCGGGAGGCAGAGGT[C/T]GCAGTGAGCCGAGAT	54476
rs569729227	snp	C/T			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622193	AAGGATTTCTCAGCC[C/T]GACTTTCCAGAGACC	54476
rs569744849	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5723976	TCAAGATTATCTGAT[A/T]AGTAAAATTAAAGAA	54476
rs569761142	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781724	CAGGAAGAACCATAG[A/C]GGCACTCCGGGTACT	54476
rs569767913	snp	A/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5723659	CTCAAAAAAAAAAAA[A/T]AAATAAATAAATGCA	54476
rs569791444	snp	A/C/G	3.4339e-05	0.0041435	missense, synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5740990	TTTCTTTCACTAGTA[A/C/G]TTCAACGAGCTCTTG	54476
rs569795158	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669161	CTGCACCTGCCAGCC[G/T]GAGAGGAATATGGGC	54476
rs569804209	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5632735	TGAGCCAAGATCACG[C/T]GACTGCATTCCAGCC	54476
rs569809907	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643055	TGTCTGGCACTGACA[G/T]GAAATAATAATGGGT	54476
rs569814461	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668894	CTATCTAGTTAGCAT[A/C]CTATCCACCTGATGC	54476
rs569835385	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5687537	GACTCTCATATTGGC[A/G]CTTGTGGACCTAAAT	54476
rs569847998	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643509	CTTCTATGCAGCCAG[C/T]GACAGCCCAGACTCC	54476
rs569852374	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5771431	AAGCATGTCTACTCA[C/T]CAAAGAAATTCAGAA	54476
rs569862655	snp	A/G	0.00159617	0.0282053	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739441	CAAAAAGTATAATAA[A/G]ATGACTAAAGACTAG	54476
rs569899042	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5627917	TATCACTAAGCTTCC[A/G]TGATAAATCCCAGTG	54476
rs569902004	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5626776	AGGTTCCTGAGTATC[C/G]CTGCGTCCAGGAAGC	54476
rs569933942	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5761855	GTATGTAAGACATGG[C/G]AAATCATCTTATACA	54476
rs569938873	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621647	GAGGTCTGTGAACTC[A/C]CAGCCTCTCAGAACC	54476
rs569939761	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5771784	CCTGGGCAATGGGAG[A/T]GAAACCCTGTCCCCC	54476
rs569942979	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5693198	ACTGGGACACAGCCA[C/T]ATTCATTTGTTTACA	54476
rs569946011	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5702375	ATTTCCACAGGGCCA[A/G]GCAGAAACAAAAATA	54476
rs569957012	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5727989	TTTCCAAACTTTCTA[C/G]TCCATTCAACCTCCC	54476
rs569970170	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5684396	ACAGGTGCGAGCCAC[C/T]GCGCCTGGCCCACAA	54476
rs569976460	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622131	GAGGCTCTTTCAATG[C/G]GCCAGCTTCAGAACC	54476
rs569993359	snp	C/T	0.00478085	0.0486577	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669176	TGAGAGGAATATGGG[C/T]GGTCGGGCTCCAGCT	54476
rs570008486	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5696246	AAAAGCAGGGCTCTC[A/G]GCAGCTGGGAAAACA	54476
rs570013800	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780771	CACGATCTAAGTACC[C/T]AGGACAGCTGCTACC	54476
rs570056114	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780352	CACAGTGCTTCTTCT[G/T]TAGGTGAACGTGTGG	54476
rs570056553	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713436	CCTGAAGTCAGAGTC[C/T]GAAATGGAGTCTGCA	54476
rs570063778	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5685486	CCAAGACACTAAGGG[A/T]TGCACACTAAACATT	54476
rs570076740	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5645683	GCAACCTCCATCTGC[C/T]GGGTTCAAATGATTC	54476
rs570097782	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5774972	TTGGTCTTGAAATGC[C/T]GACCTCAGGTGATCC	54476
rs570098977	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5656437	TCAAAACATGAAGAA[A/C]AGGGTATCGTGGCCA	54476
rs570108310	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5751595	TACACAGGAAAGGTG[A/G]CCTGAAGCAGCCTGA	54476
rs570126142	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5775636	AAACTTTGAGAGGCC[A/G]AGGTGAGTGGATTAT	54476
rs570138676	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5707645	AGTGTTATATAGCAT[A/G]GAAGTGGTGACAGTG	54476
rs570139674	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5765534	ACTCAGGAAGCTGAA[C/G]CAGGAGGACTGCTTG	54476
rs570142014	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667117	GGCCAGCCATGACTT[C/T]TAAACTATAAACTGT	54476
rs570159451	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5654983	TAGATGAGCTGATGT[G/T]TGGCTCCTAACCTCT	54476
rs570190309	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5700438	GTGAAATTTCTAACA[C/T]GCATCTCTCCCTTGA	54476
rs570191643	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5731963	CAAAGCCTTCTCCCT[C/T]ATCCTGACATCTCAA	54476
rs570253661	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5701109	GTGGGAGCACACACA[C/T]GACAGCCTCCCCCAG	54476
rs570259058	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5653360	ATTTGGGAGGCCGAG[A/G]TGGGCGGATCACGAG	54476
rs570266704	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5726718	CAAAAAATTAGCTGG[A/T]CGTGGTAGCAAGCGC	54476
rs570287644	snp	A/G	0.00914312	0.0669923	intron-variant	RNF216	GRCh38.p7	7:5755568	GCAGATAAGTTTTGC[A/G]TGTTTTTGAGTATAT	54476
rs570288544	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5690482	AATCTATCAGCTGCT[A/G]CCACAGAATGAAATT	54476
rs570294038	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5657291	GGTGAGACTGGGCCG[A/G]GTGCAGTGGCTCACA	54476
rs570323453	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5652787	AGAGTGAGACCCTGT[A/C]CCTTAAAAAAAAGAC	54476
rs570325342	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677755	TGTTGCTCAGGAAAT[A/C]CTAGGAATCAGAGTC	54476
rs570346411	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5647866	AGTGGCTTAGACTAC[C/T]GTAATGGCCTTCTAA	54476
rs570359734	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5636988	GAAAAAAGTGCTGAG[A/G]ATAGGCCAGACTGTT	54476
rs570362259	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5774658	TGGTAAATACCATCA[A/C]AATAGCTGCATTGTA	54476
rs570373431	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5779130	AGAGCTAGAATATAG[A/C]AATGCCTAGAATTTT	54476
rs570379939	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5756107	CCCCCATTCTGCTCT[C/G]GTGATAGTGAGTGAG	54476
rs570397426	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5636558	TAAGCCAGAGAACAG[A/G]CTTGTGTGACAGTGC	54476
rs570424780	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5739827	CCAACATGGTGAAAC[A/C]CCGTCTCTACTAAAA	54476
rs570435541	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5636405	GTTCACCACTTGAGC[G/T]CTTACTGTGGAGTGG	54476
rs570455551	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676329	TCCATGCCAAAGAAA[C/T]TTCTTTCTCTCCAGC	54476
rs570462974	snp	A/C	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5740299	GCCCGGCTAATTTTT[A/C]ATTTTTTTAGTAGAG	54476
rs570463109	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5735681	TGGGAGAAGAGTTAC[A/G]GAAGACAGGAAACAG	54476
rs570464547	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5688115	TTCCTGCTCTATGTC[C/G]TGGATTCCCACAGTT	54476
rs570466586	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678101	CACTCCAATGCCTGA[C/T]GCCCCACTGTGGAGC	54476
rs570472907	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667428	CCCAAGGATCACTGC[C/T]AGGAACTGAAAACCA	54476
rs570501061	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5770625	AAGAATAGATATATA[C/T]TAGATGACTTTAGAA	54476
rs570504417	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5749923	GCTGGTTCTTTTAAT[A/G]TTTTGTTTTCCAGAT	54476
rs570529250	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5765219	TTAATCCCAGGACTT[C/T]GGGAGGTCGAGGCCA	54476
rs570540996	snp	C/T	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5705726	CCAGACGGACCAACA[C/T]GGAGAAACCCCGCCT	54476
rs570551791	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5731531	CCACCCAGACCCAAC[A/G]CATGTTAACTATCCA	54476
rs570552338	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5778888	AGCTGGGATTACAGG[C/T]GCACGCCATCACACC	54476
rs570552426	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5689261	TATGGCAGCATTTTG[A/G]CTAGTTTGTGAGGTA	54476
rs570581017	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5716236	AGGGTCAGTAGCCAG[C/G]TGTAGTGGCTCACAC	54476
rs570581772	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662555	TGCAGGTAACAGAGA[C/T]AGTTTCTGCACTGAA	54476
rs570617958	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5646669	CTGCACTCCAGCCTG[A/G]CGACAGAGCGAGACT	54476
rs570630928	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5759843	TCACCATGTTGGTCA[C/G]GCTGGTCTCGAACTC	54476
rs570633962	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5764588	GGGAGGCGGAGGTTG[C/G]AGTAGGCCAAGATTG	54476
rs570638888	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5765705	CCCAGTACTTCGGGC[A/G]GCTGAGGCGGGCAGA	54476
rs570676484	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5743945	TCTATAGAGAAACAA[C/T]ATCATACAGAATCCC	54476
rs570683009	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5640177	TGCTGGCATCACAGG[C/T]GTGAGCTACTGTGCC	54476
rs570688170	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5721806	AAGGGGCTGAAGGAA[C/G]AGTACCTAGATTCAC	54476
rs570703434	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5745421	ATTTATGTCTGTGGC[C/T]ATTCGTGCTCTTCTC	54476
rs570707491	snp	A/C			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622497	GGGAGATGCTCTCGG[A/C]TGCCTTGCTACCCAG	54476
rs570708954	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5693395	GATGCTGACCCCCCG[A/G]TATGGACCTCCACTG	54476
rs570714114	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5716526	TTATCTTCCCTTCAA[C/T]TCTGATTCAGTGTGG	54476
rs570729626	snp	A/G	0.00159617	0.0282053	intron-variant, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711670	CCTTCTTATACATCA[A/G]CAGTCAGGTAAACAG	54476
rs570748400	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5657050	CCTGGAAGGTGTCCG[A/T]CCCCATGCGTGCTAG	54476
rs570753329	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5641058	CTATATTCTTCTCCT[A/T]AGTCAAATTTTGTTA	54476
rs570759831	snp	A/G	0.00318978	0.0398085	intron-variant	RNF216	GRCh38.p7	7:5765289	AACACAGTGAGGACT[A/G]TCTATACTGAAAATA	54476
rs570764839	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666160	GACAGAGTGAGACTC[C/T]GTCTCAAAAAAAAAA	54476
rs570778064	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620525	GGCCTGGAGAACCAG[A/G]GTGGGTGCTCACGGC	54476
rs570782671	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5653432	TGAAACCCTGTCTCT[A/G]CTAAAAATACAAAAA	54476
rs570788265	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5655892	GCCAGGGTCTCACTC[G/T]GTCACCCTGGCTGGA	54476
rs570796588	snp	A/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5731894	AGGTGCCAGTGTTTG[A/G]GGACCGGTTTGGAGA	54476
rs570799811	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5735212	CAGGAGTCTAAAGTC[A/G]TTTCAAACTGACACT	54476
rs570825792	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666656	AGCCTTCTGAGCTGC[A/G]CCTCTGAAGGTGGGG	54476
rs570875903	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5717170	ACCAGCCTGACCAAC[A/T]TGGAAAAACCCCATC	54476
rs570876124	snp	A/T	0.00953873	0.0683987	intron-variant	RNF216	GRCh38.p7	7:5650536	TGCTCATTTGGGTTG[A/T]CTGCAGAATTCAGTT	54476
rs570916071	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620872	TGAGGTCACCTCTTC[A/G]GCTGTGATGTCTACA	54476
rs570917528	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5656228	GAGCTGAGATGGTGC[C/T]ACTGCACTCCAGCCT	54476
rs570935379	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5720479	AAGGCTTCCTGTCAA[C/T]GGTAGGCTGTTCACA	54476
rs570936979	in-del	-/ATC			intron-variant	RNF216	GRCh38.p7	7:5715455	TCTTTATATAAAGTT[-/ATC]ATATTCAATCCCATG	54476
rs570941894	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670931	CAAGACGAACCACCA[C/T]GCCTCTCCCTTCCCT	54476
rs570960561	snp	A/C	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5688871	ATAACAGCTACTAAC[A/C]TTACTGTGCAAAGCA	54476
rs570971253	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5726086	GTTCAAGGCTTGCCC[A/G]GGCAACATGGGGACA	54476
rs570973318	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5721543	TTGTTGGTGAATGTA[C/T]GTCCGCAATTTACCT	54476
rs570986430	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5743330	TCATCATTTTTTCAT[A/C]CTGTTCTATAAACTC	54476
rs570998571	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5733579	TTGTTCTATAAATGA[A/G]CTAAGTTTATACTTT	54476
rs571004813	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5645474	CATAATTTCAACAGC[C/T]GTATCTTCAAGATCT	54476
rs571023368	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768843	TTTTTTTGTATTTTT[A/G]GTAGAGACAGGGTTT	54476
rs571032154	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5635238	GGAAGATGAAGAAAC[C/T]GAGGTCAGTTTTGAT	54476
rs571042805	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5773039	CACGCCTCAGCCTCC[C/T]ACAGTGGTGGGATTA	54476
rs571043901	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5645882	GGCGTGAGCCACTGC[A/G]CCTGGCTGGTTTCTT	54476
rs571061777	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5763746	AGCTGAATTTTTAAA[A/G]TTTTTTTGTAGAGAC	54476
rs571068933	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5693865	AGACTCTCTGGCCAA[C/G]AAGGAGATGCTATTT	54476
rs571071833	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671526	AAGGACAGAGAGAGC[A/C/T]GGGCACGGTGGCTCA	54476
rs571092495	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5629256	CTGAGGCAGCAGGAT[C/T]GCTTGAGGCCAGGAT	54476
rs571110576	snp	A/G	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753443	ACACAAACTTTAAGA[A/G]TCATTTAAGCAAACC	54476
rs571127264	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5683877	ATTACAGAAAAAAGA[C/T]AAACACCACATGAAT	54476
rs571128661	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5623822	GAGCTCAAACCCACC[C/T]CTTGGGACTTCCTCA	54476
rs571131746	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5773491	CGTGATTTCCCCGCC[C/T]TGGTCTCCCAAAGTG	54476
rs571135986	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5705410	ACATGCAACATATCA[A/C]CTTCTAATCCTCTAC	54476
rs571147969	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5729164	CAGCATTAGAATGCA[C/T]CTTTCACACTCCTGC	54476
rs571161560	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5724095	CTGAGACAGGTTTAT[A/G]ACCTGACAGCAATGT	54476
rs571171696	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672961	AAAAAGTACTGAGAT[A/G]TCCTGGCTACAGCTC	54476
rs571187234	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5689493	CCACTTTCTGGAGGC[C/T]ATTTTCTAAAAAAAA	54476
rs571194891	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5748752	ACTAAGTAGTTAAGG[C/T]TTTGGTCAACAGTAT	54476
rs571200010	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5705854	GGAGGTTATGGTGAG[C/T]CAAGATCATACCATT	54476
rs571215911	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619982	TTAGACCCAATCACT[C/T]GGACGAATCTGTCGG	54476
rs571219975	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5707221	TGTTCTTCTTTCTTA[A/T]GACTGTCTAGGATAT	54476
rs571222558	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5724861	TAACCTCTTCAAAAG[C/G]GTTTTCAGCAGTTAT	54476
rs571228746	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676300	TTGACCACCGCGGCC[A/G]GCCTCAAGTTCTTTC	54476
rs571269078	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5751473	AACCTGGGAAGTTCA[C/T]TTGATCTTCCTAGAA	54476
rs571269447	snp	G/T	0.00676609	0.0577691	intron-variant	RNF216	GRCh38.p7	7:5708949	GGGTCCTCTGGCGCA[G/T]TACAAACCACCCAGC	54476
rs571274663	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682144	CTGCTAGGAAAAACC[A/G]TTGGCTTTCTTTCCC	54476
rs571290517	snp	C/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5777147	CTTCCAGCAGTCTTT[C/G]ACAAGGCATGTGAAC	54476
rs571291830	snp	A/G	0.0150606	0.0854603	intron-variant	RNF216	GRCh38.p7	7:5687338	GAGGCGGAGGTTGCA[A/G]TGAGCTGAGACTGCG	54476
rs571298850	snp	C/G	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5749119	CCATTTGGAAAACAG[C/G]TGTGTTCTGATCAGC	54476
rs571307928	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5697506	GGGGCCAAACCCTCA[C/T]TGGCCTCTTCTGTAC	54476
rs571319118	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5715527	GTGATTATAAACAGC[A/C]AGGATAAGGAGTATG	54476
rs571325546	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5777743	CATTATGGATATAAA[C/T]ATGCAAACAATTAGT	54476
rs571328099	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5733401	GAACTGTAAGAGAAG[G/T]TATCAATTTGATTAC	54476
rs571337999	snp	A/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5682469	CTGCAGTGCAGTGGC[A/G]CGGTCTTGTCTTACT	54476
rs571340729	in-del	-/AT	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681952	GCTACAAAGATGACC[-/AT]ATCTCCCTGTGCCAC	54476
rs571367300	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5692418	CCTTGTTAGTCAGAC[A/T]TACTCTGTGGGAAAA	54476
rs571371072	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5710134	GAAGGCTGAGGTGGG[C/T]GGATCACTGGAGGCC	54476
rs571379299	snp	C/G			upstream-variant-2KB	RNF216	GRCh38.p7	7:5783017	CGATCCTGGGCAATA[C/G]AGTAAGACCCCATCT	54476
rs571382521	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5703011	GGAGCGTCCTTCTGC[A/G]GCCTGAACCTGAAGC	54476
rs571383829	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5659643	TTTGCTGGGGTTGTA[A/G]GACCTTGCAGCACCC	54476
rs571384159	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5709377	AGCGTCACAAATTCC[C/T]CAGCCTTTGATGCAA	54476
rs571395199	snp	G/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673979	AATTCTCCTGCCTCA[G/T]CCTCTGAGTGGCTGA	54476
rs571429463	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5733876	ATTCACACATATAAG[C/T]TGCTTTTTAGATGAG	54476
rs571433163	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5698090	AGTACTTTTATGAGG[C/T]TATGGGGATTTCATC	54476
rs571452133	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5691138	ATTTCTCTAACCGTG[C/T]GTGTAGACGGTGAGC	54476
rs571496169	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5691560	TGTGTGTGAGAAAAA[C/T]AGAGTATGTGTGTTA	54476
rs571497798	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5763215	ATGAGGGAACCTTTC[C/T]GGGTTAAGTCACACT	54476
rs571502071	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5757280	TATATTTTCCTATCA[C/T]GTTACTAAGTATACA	54476
rs571508160	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5686408	AACAGGATCCCCATT[G/T]CTCTGATGAGGAAAG	54476
rs571525673	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5638689	GTCACCCAGGCTACA[C/G]TGCAGTGGCAAGAAC	54476
rs571529694	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5711303	CAGTCAAATAAATAA[C/T]CTACCAGATGTGATG	54476
rs571529768	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675052	TGTCGGTACAGAATG[C/G]CAACTGCTGAAAAGC	54476
rs571562586	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5633642	TTAACAGGGAGGGAG[A/G]TTTGTTTCCTTTCCT	54476
rs571566177	snp	C/G	0.000798403	0.0199641	utr-variant-5-prime, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781602	CTACCGCGCCGCTTA[C/G]TCCTCAGAAGCCGCA	54476
rs571573756	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5761760	CACTGCACTCCAGCC[C/T]GGGCAACAGAGTGAG	54476
rs571577858	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5748218	AACCAGTTTCTGCCA[A/G]CTTATAGAGGCTGCA	54476
rs571599906	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5771956	AAACCACAAGGGGCC[A/G]GGCGTGGTGGCTCAC	54476
rs571621313	snp	A/C	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5772187	GCGGTGAGCCGAGAT[A/C]AAGCCATTGCACTCC	54476
rs571627384	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5776664	TTCACAGGAATAGCC[A/G]TATCAAGCTAAAGTG	54476
rs571627957	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5639177	TAACATTCCTTAAGA[C/G]ATAGGGAAGCAGGCT	54476
rs571629070	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5742110	GGAGTGCAATGGTGC[A/G]ATCTCGGCTCACTGC	54476
rs571651191	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RNF216	GRCh38.p7	7:5781945	GATGTTTACTCGATA[C/T]CTACTGATTTGCCCT	54476
rs571653202	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5776665	TCACAGGAATAGCCA[C/T]ATCAAGCTAAAGTGA	54476
rs571654252	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767579	TGAGCAGAAATCTCA[A/G]CAAACATGTATTGTT	54476
rs571654700	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675497	ATTTAAAAAAATTAG[C/G]TGAGTGTAGTGGTGC	54476
rs571672862	snp	C/G/T	0.00319074	0.0398324	intron-variant	RNF216	GRCh38.p7	7:5655836	CTCAGCAAATGCTTA[C/G/T]GCATATTACGAAGAA	54476
rs571700269	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5761262	AAACATATCCAAGGA[A/G]GTGGGTCAAAAAAAA	54476
rs571709550	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669759	TAGTCCGACATGGTG[C/T]TGTGCACTTGTGATC	54476
rs571717559	in-del	-/A	0.00874735	0.0655527	intron-variant	RNF216	GRCh38.p7	7:5740001	AGTGAGACTCGGTCT[-/A]CAAAAAAAAAACAAA	54476
rs571730991	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5632413	AATGAATTCTCAGCA[C/G]AGCTCCTTTCTGATG	54476
rs571733272	snp	A/G	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5685193	TACAATGTCCACCAC[A/G]GATGGGTGGGCATGG	54476
rs571751950	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5631459	CTCCCTGGGTCACTG[C/G]TCTCCAGTGGCCTCT	54476
rs571762319	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5633900	ACAAACATCCTCCCT[C/T]AGCTTGTCCCTCCAC	54476
rs571781525	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5752378	GTTCTTGGTTAGAAA[G/T]AGTAGTATCATAAAA	54476
rs571781687	in-del	-/AAAAAG	0.00835141	0.0640778	intron-variant	RNF216	GRCh38.p7	7:5728579	CTCCGTCTCAAAAAA[-/AAAAAG]AAAAAGAAAAAGAAA	54476
rs571794098	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5652601	TATGAAATGAGCTTT[A/C]CTTGGCTTGAATTCT	54476
rs571812232	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680709	GCCCAGCACTCAACA[A/C]TTCTACTTGGATATC	54476
rs571828915	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5649169	GGGGGATCACTTGAG[C/G]TCAGGAGTTCGAGAC	54476
rs571841488	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5718516	AAAACCAATTCTCTA[A/G]AAGTTCAAAACAAAC	54476
rs571848038	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5720098	GCTCTACGACACTGG[C/T]CTGATTCATGCCAAG	54476
rs571852509	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713890	AGAGGAAGAAACAGT[A/G]GCTTAAGGAATTTAA	54476
rs571865448	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5639323	AATGCTGGAAGCAAC[C/T]GGATCCCAGATAAGA	54476
rs571869154	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5740482	GATGACAGAAACACT[A/G]TCCTCCATGCTTGAT	54476
rs571888188	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5764965	ATCCCAGCTACTCCT[A/G]AGGCTGAGGCTAGAG	54476
rs571889579	in-del	-/CTTTT	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5769121	TACAGTTCCAAATGC[-/CTTTT]TTTTTTTTTTTTTGA	54476
rs571889971	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667678	TCCCAGGGTTTTGCT[A/G]GGAATCTTGGCCTGG	54476
rs571895859	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5721548	GGTGAATGTATGTCC[A/G]CAATTTACCTGCGAA	54476
rs571899281	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5703046	CAGAGGGACCCATGC[A/T]GGGCTCTGAAGAAAG	54476
rs571931867	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621940	CCACTGAGAACACCC[A/G]GGGCACACACGGGGC	54476
rs571958999	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5740040	AAAACAAAAAAAACC[C/T]GCCTGGGTAAAGTAG	54476
rs571965724	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662690	GGATCGGTATAAAAC[A/G]AAGCCCTTGTCCTCT	54476
rs571967428	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5649570	CTTTGGTCCCAGAGG[C/G]GCTATATGATAAGGA	54476
rs571967561	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643549	CTGTGCTCACCACCA[A/G]CCAGTGTGTGGGTAA	54476
rs571975007	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5653001	AAAACACAGTAGCAC[A/G]AGCTGCTTGGCAGGG	54476
rs571978069	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5760280	CCAGCACTTTGGCAG[A/G]CTGAGGCGGGCGGAT	54476
rs571999058	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5755809	GATACATTCTAGGAG[C/T]GGAAATGCTGAGTCA	54476
rs572014960	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5760786	TTGCCAGCAAATTAA[C/T]AGCTTATTAATCCAT	54476
rs572020751	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5726456	CACCTATATCCACCC[A/C/T]ACCCTGTAACAGGAT	54476
rs572033861	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750892	TGCGAGATTACCTAC[G/T]AACTCAACAGAGAAG	54476
rs572058975	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5717968	CACCTGTAATCCCAG[C/G]TACTTGGTCTGCTAC	54476
rs572062960	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5751318	AGGTCCTGGGTGAAA[A/G]CCTAACAAAAAGGGA	54476
rs572069948	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5647180	TAATTCTTGCTCTGG[C/T]GGGAGATAGGAGTTT	54476
rs572084472	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5724477	GAACTCTGGCTAAAT[C/T]TGGCTGAATGAAAAA	54476
rs572084527	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5747833	TCCCAGGCTGAAGTA[C/T]AGTGGCACAATCATA	54476
rs572094195	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643859	CTTGCCCTGCAACCC[A/G]CAGCGTGCTTTTGGG	54476
rs572097800	snp	A/C	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5653512	AGGCTGAAGCAGGAG[A/C]AAGGCGTGAACCCGG	54476
rs572109005	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5722605	CTGTGTTAGCCAGGA[C/T]GGTCTTGATCTCCCG	54476
rs572111794	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672292	CTGCCCCTAAATACA[G/T]GTTTACTTTGGGGGA	54476
rs572129991	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5770726	GATATTGTATTACTA[C/T]TAAGTTACACTAATT	54476
rs572142439	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5745527	GACAGATCAGATGCA[A/C]GTTTTCAAGAAATTA	54476
rs572153625	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5648024	ATAGCTCTGGGTGTT[C/T]TGTAATTTGAGATGC	54476
rs572157154	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5642257	TTGCTCTGTCACCTA[A/G]CCTGGGGCACAGTGG	54476
rs572170396	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5700582	CACAGGCTGTGACAA[A/G]CCTGAGAAGCAATAG	54476
rs572182905	in-del	-/T	0.293551	0.246177	intron-variant	RNF216	GRCh38.p7	7:5640061	ACCGCGCCCGGCCAA[-/T]TTTTTTTTTTTTTTT	54476
rs572192329	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5648814	AACCAGCCAACTCTA[A/G]AAGACATTCTACAGG	54476
rs572195117	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5736170	CCTCTGATGCCCAGC[C/T]GAAGCTGGACTGTAC	54476
rs572198788	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5693935	AATAACTGTTCTATA[A/C]GATGGAATTCACTTG	54476
rs572231794	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681657	GAGTCCCATTCCTCA[A/G]CTGGGGATAGTTTTC	54476
rs572232444	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5739994	GGTGACAGAGTGAGA[C/T]TCGGTCTCAAAAAAA	54476
rs572236977	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5707004	GCATGTGGATATTCA[A/G]TTTACAGAGCACCAT	54476
rs572243791	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5631878	GTAGAAGGTCACGCT[C/T]TGCCCCCACGAGGTC	54476
rs572246684	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216, RNF216-IT1	GRCh38.p7	7:5662213	CTTTCTTACTGGTAA[C/T]GATAGGAACCTGCTA	54476
rs572255732	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5731932	TGATTCTGCAGCCCC[C/T]GCCGGGGACCCACGT	54476
rs572266748	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5657398	CAGGGAGAAACCCCA[C/T]CTCTACTAAAAATAC	54476
rs572276772	snp	A/G	0.00874735	0.0655527	intron-variant	RNF216	GRCh38.p7	7:5626413	CTAAGAAAAAAGACT[A/G]AAAAAAAAAAAAAGA	54476
rs572280896	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667264	CTGTTCCACCTATAT[A/T]TATTTATGTTTGGAT	54476
rs572282161	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5725513	AGGCAATCCCTGAAT[C/G]CCATTTTAACACAGT	54476
rs572284119	snp	A/G	0.000555302	0.0166536	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5730763	ACTGGGATTTATAAT[A/G]ATTCTGTCTTCTCTC	54476
rs572333421	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5651371	AGCTGGGACTACAGG[A/T]GCGTGCCCACCACTC	54476
rs572334106	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5726479	AACAGGATGCTGGAG[C/T]TCAAAATCCTTCCAC	54476
rs572345759	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5725895	AAATAGGCAGCATTT[A/C]TTTATTTTCATTTTC	54476
rs572349629	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621446	GGGAGCCACCGCGCC[A/G]GGCCATCTTAGATCT	54476
rs572370530	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5773855	AACAGGCGAGTCACC[A/G]TGCCTGGCCCCAAGC	54476
rs572378352	snp	C/T	1.65233e-05	0.00287426	intron-variant	RNF216	GRCh38.p7	7:5716691	TGAAAATGCCCAGAA[C/T]AAACAAGGTGAGATT	54476
rs572396115	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5651630	AAGAGATTTCAGTAT[C/T]ACTTCGGTCATTGCA	54476
rs572405777	snp	C/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768623	CAACAGTCAATAAAA[C/G]ATAATTAGGTAATTC	54476
rs572415121	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5626952	GGAGACACCCACAGT[A/G]TTTCTTTCAGGGGTC	54476
rs572444867	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5641915	GTGCACACCTGTAAT[C/T]CCAGCTACTTGGGAG	54476
rs572459827	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5684386	TCCTGGGATTACAGG[C/T]GCGAGCCACTGCGCC	54476
rs572478913	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5630099	AGAAGGAAAGAGGAT[A/G]AGGAGGAGCCAGGGG	54476
rs572484882	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5636747	GGCTATCAGAGGAAA[C/T]TGGAGGGATTTGTAT	54476
rs572491268	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5775024	GTGGTGAGATTACAG[C/T]CGTAAGTCACTGTGC	54476
rs572494201	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5779455	AAACCAAGGCAAAGC[C/T]AGGCCATGTATTAGC	54476
rs572498205	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711371	AGCGTCGTTTGGACT[C/T]TGAAAATGGCAAAAG	54476
rs572501727	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5636294	TGACTGTTCGCTTCT[A/G]GTTTTTTGCTTCCTA	54476
rs572544650	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5770194	GGGCTGGGCGCCGTG[A/G]CTCACATCTGTAACC	54476
rs572560536	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5706277	AAAAACTACCCAATT[A/T]ACACATTTTTAAGTG	54476
rs572565391	in-del	-/T	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5750324	TTCCTAGCAGAGACA[-/T]TTTTTTAAAGACCAA	54476
rs572568415	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5730327	CAGTGGTAGGTATAT[A/G]AATGATCAACGTAAA	54476
rs572576786	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5683011	ACAACCTCCCATGAC[A/G]GGGTCACAAACTCCT	54476
rs572583622	snp	C/T	0.00716266	0.059414	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620593	CTCAGGAATCAGGGA[C/T]CCTCCAAGGAAAGAG	54476
rs572591162	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5721400	TGTTTATGCTCCAAT[A/T]GGAAGGCATCTCCTA	54476
rs572595279	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5771667	AGCCAGGCGCAGTAG[C/T]GGGCACCTAGTCCCA	54476
rs572639006	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5688645	AGCAGAAGGCTCACT[C/G]TGCGCACCTTACCTT	54476
rs572650039	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5639977	TGTTAGCCAGGATGG[A/T]CTCGATCTCCTGACC	54476
rs572654188	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5721664	TCCATCAGCAATGCA[A/T]GTGAGTTCCAGTCTC	54476
rs572659392	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5759381	TCCTCTTCAGCCTAC[A/T]CAATGTGAGGATGAT	54476
rs572673952	in-del	-/T	1.82735e-05	0.00302265	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622837	AAACGGGCTTTGTGC[-/T]GCTCAATGGGGATTC	54476
rs572687452	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5770590	GATGTGTAGATTTAA[C/T]ACAACCTTTATCAGG	54476
rs572704702	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677208	CAAACACATGTGATT[C/T]AGAGACTGCTCAGCA	54476
rs572710614	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5734260	GGTATAAATGGAATA[C/T]CATTTAGCAATGGAA	54476
rs572717003	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5716375	ATTAGCTGGGCATTT[A/T]TTTTACATACAGAAA	54476
rs572725111	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5683731	TTAGGAATTACAACT[C/G]TTTTTAAAGTGCTCA	54476
rs572729923	snp	A/G	1.66466e-05	0.00288496	intron-variant	RNF216	GRCh38.p7	7:5715206	CTGCAGGCAGTCAAG[A/G]AACACACATGAAATG	54476
rs572738966	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5624554	CCTGGAAAAGTCTTG[C/G]AGATGTCCTCAACTG	54476
rs572777363	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5736897	GGCAGCCGCCCCGTC[C/T]GGGAAGTGAGGAGCC	54476
rs572794593	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5660584	CATGGAGCCCTGTTT[C/T]AATGATTGACTGAGA	54476
rs572809568	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5778990	CTTAGGTGATCTGCC[C/T]GCCTCGGCCTCCCAA	54476
rs572843141	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5734756	CTGAACCTGGGAGGC[A/G]AAGGTTGCAGTGAGC	54476
rs572844513	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5758880	GAAGACGCAATTGTA[C/T]TTAGCAATGTGAGAA	54476
rs572851336	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5660951	GCCTTAGGTTTTTTT[G/T]TTTTTTTTTTTTTTT	54476
rs572856497	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665932	GCACTTTGGGAGGCC[A/G]AGACAGGCGGATCCC	54476
rs572863206	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5692539	GGCTGTATCCTGTCC[A/G]ACAGTGCCAGAGCTT	54476
rs572871719	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5699201	CCCTCCTCCTTCAGT[A/G]TAATTTTGAAGCAAA	54476
rs572894360	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5649584	GGGCTATATGATAAG[G/T]AAAGGCAAGTTGAAG	54476
rs572941978	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5763833	CTGCCTTGGCTTCCC[A/G]AAGTGCTGCGATTAC	54476
rs572972791	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5777957	ATCCTCATGTGTGGA[A/G]GGTAAAATCAACGTT	54476
rs572994979	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782473	GTCCATAATCCCCGC[A/G]CTTTGGAAGGCCAAG	54476
rs573012876	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5693490	AGAATAAAATTAAAC[C/T]CCTTTAATGCTAAGA	54476
rs573019147	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5764149	AGTAAGCTGAGATCA[C/T]GCCATTGCACTCCAG	54476
rs573034065	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5783024	GGGCAATAGAGTAAG[A/T]CCCCATCTTTACAAA	54476
rs573071249	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5699066	AACTTTTTATTGTAG[A/G]AAATTTTAAACATAT	54476
rs573107958	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5632805	CGAAGCCCTCCAGTG[C/T]CCCATCGCTACTCCA	54476
rs573112111	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5743595	ATGATTCCATTTACT[G/T]AAAATATGTCAATAA	54476
rs573121012	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767169	CCACTACAGAAAGGA[C/T]GAATATATAAAACAC	54476
rs573132186	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5777016	TGAGCACAACAGCTT[A/T]CACTTAGGGCTCCTG	54476
rs573139163	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5758085	AGAGTATACATACTC[A/G]TCTAACAAAATATAT	54476
rs573156641	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5623999	TCAGGGAGGCCAGCA[A/G]AAGCCTGCATGGCCT	54476
rs573158242	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5762515	TTAAAAAATAATAAT[A/T]AATAAATAAATAATA	54476
rs573167410	in-del	-/A	0.280256	0.248162	intron-variant	RNF216	GRCh38.p7	7:5764211	AAGAATAAACTAATT[-/A]AAAAAAAAAAAAAAC	54476
rs573197036	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5724540	GCCACAGGCCAGGGC[C/G]AATGTCATGTCAGCA	54476
rs573213118	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5720153	TACAAACTCAATATG[C/G]TGAAAAAGCAAATAT	54476
rs573215596	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5698241	TTCTTCTGGTTGCAG[C/T]TGGACTGCATGTAAG	54476
rs573216453	snp	A/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768585	AATTTTGAAGGCTTG[A/T]AATCACACAGCATGT	54476
rs573242370	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5724986	AAGTCTGGGTAGTTT[G/T]TACCTAATAACACAG	54476
rs573244028	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5695458	GCTGCCTCGGAGCCC[A/G]GACTAAGCAAGGCTG	54476
rs573251405	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5692056	AGGTATAATTTCCGA[C/T]ATTCCTACCCAGAGT	54476
rs573260481	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5758581	CCAGTGTGCCATGAA[C/T]GTGAGATGTGGAGTC	54476
rs573277198	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5721892	GTAAATGATCTGTTT[A/T]GGTTTTGTACTTGTT	54476
rs573278237	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5645020	AGGCGTTTCATCATA[C/T]TGGCCAGGGTCATCT	54476
rs573282122	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681819	TGACTACATAAACGG[G/T]AAACACCCAGAAAAG	54476
rs573301287	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5747398	AAGCAGAATATTATT[G/T]TCCTGAGGATGATAT	54476
rs573301855	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5655159	CACAGGCCCACCAGG[G/T]CAAAATGACCTGGCC	54476
rs573302868	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674874	TAGTGGCACGCACCT[A/G]TAATCCCAGCTACTC	54476
rs573303548	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5720635	CGCAGACCCCCAAGA[A/G]AGTCTTGGGAAACCC	54476
rs573314983	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5737330	TGAAGGCAGCATGCT[C/T]GTTAAGAGTCATCAC	54476
rs573338092	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5747874	GCCTTGAATTCCTGA[A/G]CTCAAGTGATCCTCC	54476
rs573348139	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5699795	GCCACAGATACAGAC[A/G]CACATTTTCTAACTG	54476
rs573357314	snp	A/G	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5763362	AGGGCTAGGAGCGAT[A/G]GCTCACACCTGTAAT	54476
rs573359882	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5650333	GGTGGGCTATGTGTG[A/G]CAGACCAAGACGCTG	54476
rs573362796	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5637547	CTCTCAGGATTATAC[A/G]TTTCTTTCCCTTTTT	54476
rs573374488	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5626942	GTGCACACTGGGAGA[C/T]ACCCACAGTATTTCT	54476
rs573376174	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5650712	TTTGTTTGACTCTTC[A/G]TCCCACACTAAGGAC	54476
rs573383039	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5624270	GCCTGGGCTGCACAC[C/T]GTTCCTTCCTATTTC	54476
rs573385113	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5748534	GGCGTGAGCCACCGT[C/G]TCCAGTTTCTTTATG	54476
rs573396190	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664660	TCCCCAACACCCCCA[A/G]GGGCTGTGGAAGGCC	54476
rs573427745	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5633749	TGCAGGTAGGGTGGG[C/T]GGGAGGAAGACGCAG	54476
rs573434325	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665095	GAACCACCGCACCCA[A/G]CCAGGACACACAAAA	54476
rs573435343	snp	C/T	0.00636936	0.0560724	intron-variant	RNF216	GRCh38.p7	7:5645751	GCCCGCCACCACATC[C/T]AGCTAATTTTTGTGT	54476
rs573445101	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5697269	ATGTTCCTCACAGCA[C/G]TCACCATCACTCTCT	54476
rs573481897	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5727584	ATGAAATAAAAAGAT[A/C]ATCCAGGTGTGGTGG	54476
rs573487584	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5623588	GCAGATGTGAGCCAC[C/T]GCACTTAGCCTCTTT	54476
rs573507279	snp	A/C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5772470	GGAGTGCAGTGGTGC[A/C/G]ATCTCGGCTTACTGC	54476
rs573517986	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643724	CTCTAACGTATACAA[C/T]TCAGGGATATTTTGA	54476
rs573524048	snp	A/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5733075	CTGAGACTGAGCTAC[A/T]ACAAAATCCCAGCCT	54476
rs573543039	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5728115	GCAGATGTTTATACT[A/G]GTTCTCACCCCAATA	54476
rs573544198	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5728964	GGCCTTTAAGTGCCA[G/T]CTATTTTAGGATCCT	54476
rs573545678	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5680442	GAGTCTTGCCCTGTC[A/G]CCAGCCTGGAGAGCA	54476
rs573560744	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5733584	CTATAAATGAGCTAA[C/G]TTTATACTTTTCTCT	54476
rs573568691	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5634121	TGCCAAAGCCTTTAC[A/G]GTCCTTTTGAGACTT	54476
rs573582793	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680799	GTATCCCTGAAGGAC[A/G]CAGCCACCCACTGGC	54476
rs573590487	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5655410	AGAGACCAGCCTGGC[C/T]AACACGGAGAAACCC	54476
rs573602333	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5776374	GGATCACGAGGTCAG[C/G]AGACGGAGACCATCC	54476
rs573605853	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5703434	TAGCTGGTCCACACT[C/T]ATTTACATTCTCTTC	54476
rs573622195	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5649340	GAGGTCGCAATGACC[C/T]GAGGCACTCTAACCT	54476
rs573646692	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5776744	ACTCTACTAAAAAAA[C/T]ACAAAAATTAGCTGG	54476
rs573651000	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5632488	ACCAAGGTGTCCCTG[C/G]ATCAGCAAGGGCTCA	54476
rs573652669	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5638365	ACTCAGTGAACAGTG[C/T]TGCAGACAGAACTTT	54476
rs573675028	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5742230	TTTTGTGTTTCTAAG[A/T]GAGATGGGGTTTTGC	54476
rs573685435	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5771982	CTCACGCCTGTAATC[C/T]CAGCACTTTGGAAGG	54476
rs573694614	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5638821	TGATATTTTGTAAAG[A/G]TGGGGGTCTCACTAT	54476
rs573699387	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5781774	GCTCACCATAGAGAG[G/T]GCCGCCTAGTCGCGC	54476
rs573707572	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713608	GCTAACTGGCTCCTA[C/T]GCACCTAGAGTCAAA	54476
rs573732143	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5646351	TGCACTCCAGACGGG[C/G]TGACAAGGCGAGACT	54476
rs573738523	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5761922	GAATAGCAATTAGCA[A/C]TACGCCCTAAATTAC	54476
rs573761958	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5756424	GAGGCTAAAATATTA[A/G]CTACTTAGCTCTTCA	54476
rs573771462	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5708615	TGCAAGAAGATTTTG[C/G]TAAATCGTAGGCTAA	54476
rs573771541	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5714093	CTAAGCCTCCCGAGT[A/G]GCTGGATTACAGGCA	54476
rs573785575	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5632790	CTCCAAAAAACAAAA[C/T]GAAGCCCTCCAGTGC	54476
rs573790170	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5709241	TTGAGCAGCCTCCTG[A/G]AAGGTCTGAATATTA	54476
rs573814681	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5633404	AACACGGTGAAACCC[C/T]GTCTCTACTAAAATA	54476
rs573832815	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5690796	TGCCCCGACAGCCTG[C/T]AGGGATGTACACACG	54476
rs573841262	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5696348	AAATTAAGCTTATTC[C/G]ACATGCCTTCGGCTG	54476
rs573866502	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5648906	ACATGTAAAGCTAAT[C/T]TGAGATAATTAGTGG	54476
rs573871219	snp	G/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670667	GTCCGACAACCTAAG[G/T]TGACCTTTGGAAGCA	54476
rs573884079	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5770966	GCATGCACCACCACG[C/G/T]CCGGCTAATTTTTGT	54476
rs573908135	snp	C/T	3.30458e-05	0.0040647	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741035	CTTCTTGCCCCCAAA[C/T]GTTTTCCAAATTGGG	54476
rs573921960	snp	G/T	0.00199481	0.0315187	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667659	CTTGGGCTACCTCTG[G/T]GCTTCCCAGGGTTTT	54476
rs573929737	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5714029	TTTTTCTGAGACAGA[C/G]TCTCGCCCTGTCACC	54476
rs573951831	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5701351	ACCTGCCCACTTTAG[C/G]GGAACTCCATGCTCT	54476
rs573985828	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664865	CAATGGCACAATCTT[A/G]GCTCACCGCAACCTC	54476
rs574063300	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5621109	CCCTTACCCCAGGTC[C/T]AGGTGACCACCTGTC	54476
rs574063845	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5657907	AAGGGAATCCAAGAA[A/C]CTCTATTTTTCCTAG	54476
rs574070877	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5627176	CTGAGAAAGTACCTT[C/G]TTCAATGTTACGGCT	54476
rs574104046	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5756504	GGTTCAAGCGATTCT[C/T]AGGCCTCAGCCTCCT	54476
rs574144582	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5685138	TCTGCCTCTCTACCT[C/T]ACTGGAGGCTCATGG	54476
rs574153183	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5691914	GTCAAGACAAGTAAT[G/T]AAAGACAGACCCCAG	54476
rs574157092	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679163	CTCCTAACAGACTTT[C/T]CAGGAGGATCCTGTC	54476
rs574160561	snp	C/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754794	GAACTTTGGGAGGCC[C/T]AGACAGGCAGATCAC	54476
rs574181806	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5780036	CCCTGTGCCTGACTA[C/T]TGCAGGAAGATGGAG	54476
rs574214242	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5717024	AACACTTTGAACAGC[A/C]AAGAATAGCATCAAC	54476
rs574220598	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5690004	TTATTTGCCGAGTTC[A/G]CCTGTATTATATTTT	54476
rs574241878	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780540	CGTCTCTACTAAAAA[C/T]ACAAAAATTAGCTGG	54476
rs574276700	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678567	ACCTCAGGTGAGTGA[C/T]CTCACCTCTCCCAGC	54476
rs574278759	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750852	TAACCTGCACTCCCC[A/G]CTTTAATTTAACCCA	54476
rs574282990	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5775702	CGGTAAAACCTGTCT[C/G]TACTAAAAATACAAA	54476
rs574284441	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5707091	AGCTGATCATAAATG[C/T]GTGGATTTATTTCTG	54476
rs574298361	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5749038	CTTCAATCTTTTATC[A/C]GAAAAACAGGACCTA	54476
rs574314421	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5722145	GTCCAGGCTGGTCTT[C/G]AAGTCCTGGGCTAAA	54476
rs574315461	snp	G/T	0	0	intron-variant	RNF216	GRCh38.p7	7:5746305	GGACTTTTGGGAATG[G/T]GGGGGCTCACAAATC	54476
rs574326389	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5702544	GTGGGAAGGGAGGCA[A/T]GCAACATTTGCCTTT	54476
rs574350421	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5764355	AAACAAAGATAAAAA[C/T]AGACTCTTCAGGCTG	54476
rs574373437	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5742505	AATGAAAAATTAAAA[C/G]AAGACAGTATTTTTT	54476
rs574376213	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5700026	TTAGGCTTTGCTCTC[A/G]TCTTGCTCGATGCCC	54476
rs574396678	in-del	-/A	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753053	TAAGTTTTTCCTGAC[-/A]GGGGTACAGCCTAAA	54476
rs574407047	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5726789	AGTGAACCTGGAAAG[C/T]GGAGGTTGCAGTGAG	54476
rs574417416	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5726444	CTTCTCTGTGTGCAC[A/C]TATATCCACCCCACC	54476
rs574437744	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5764815	CTCATGCCTATAATC[C/G]CACCACTTTGGGAAG	54476
rs574461325	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5755662	TCTTGTATATAATCC[A/G]CTATATGAATATAAC	54476
rs574466577	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5731166	GCAGCTACTCTTTGT[C/T]GAGAAAACTATGAAC	54476
rs574469612	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5722581	ATTTTTAGTAAAGAC[A/G]GGGTTTCACTGTGTT	54476
rs574486822	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5749431	GCTGGGATTACAGGC[A/G]TGAGCCACCACGTCG	54476
rs574496569	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677310	ACTGTATGGGTGGTC[G/T]GGGCAATGCCATCTG	54476
rs574503610	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5764898	CTTGGTGAGACCCCA[C/T]CTCTACAAAAAACTG	54476
rs574511522	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656971	GAATCCAAAAGAAAA[C/T]CTGAGCCCACAGGCC	54476
rs574525528	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5750111	TTGCATATCTGTCCT[C/T]TTAATAAAAGGACAC	54476
rs574532465	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739451	AATAAAATGACTAAA[A/G]ACTAGAAAAGGGCTG	54476
rs574549160	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5706178	TGAGCTGAGATTGCA[C/T]CACTGCACTCCAGCC	54476
rs574558151	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5722580	TATTTTTAGTAAAGA[C/T]GGGGTTTCACTGTGT	54476
rs574558191	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677822	AGAGTAACTAAATCA[G/T]AATCCAGTAGAATCA	54476
rs574559985	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671687	GCGGGCACCTGTAAT[A/C]CCAGCTATTTGGAAG	54476
rs574566364	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5763216	TGAGGGAACCTTTCC[A/G]GGTTAAGTCACACTC	54476
rs574590393	snp	A/C	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5739963	AGCTGAGATCGCACC[A/C]CTGTACCCCAGCCTG	54476
rs574591824	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5750531	GCACTGTTCACTGAG[A/T]TTTTATTATCTACCT	54476
rs574623381	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5749874	TGATAAAAGAAGAAT[A/C]ATGGGTTTTTATGGC	54476
rs574628374	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5778577	CATATCGGATGGCAC[A/G]GTAGATGATCTTCAA	54476
rs574631295	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5706561	GTTAGTATGTGCCAG[A/G]AGTTCCTTCTTTTCA	54476
rs574659097	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216, RNF216-IT1	GRCh38.p7	7:5662125	CTGCAGCTGTGCAGG[A/G]TGTCTGCTTCCTGGA	54476
rs574664086	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5631376	GGAAAGCTCATAACC[C/T]TCATCTCTTGAGCCA	54476
rs574674246	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5723938	AATCAAGTGTAATTT[C/T]TATCTTATACTTCCA	54476
rs574715426	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5750827	CACCATCAGTAGTAG[C/T]CTCTGCAGATAACCT	54476
rs574729874	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5735414	ACAATCAAACTCACA[A/G]AGAAGCTATGTTTAT	54476
rs574739341	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5660899	AACAGAGGTCTAAAA[C/T]TCCTGCTTTTCACAG	54476
rs574746720	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5683592	AGTTTTGTGATGGGA[G/T]AGAGGTGCCAGTTGC	54476
rs574754238	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656033	CAGCACTTTGGAAGG[C/G]TGAGGGGAGCGGATT	54476
rs574766230	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5735701	ACAGGAAACAGCTAC[A/G]AAATTTCCAGAACTG	54476
rs574767502	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5682911	TTGCATTGCGTTAAT[A/G]TAGCATCAAAACCAG	54476
rs574775072	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5744512	TTCAAATAACCATTC[A/G]AACTAAATAAGGGAA	54476
rs574784043	snp	A/G			utr-variant-5-prime, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781592	GCGGCCTTCGCTACC[A/G]CGCCGCTTACTCCTC	54476
rs574798680	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656523	GGAGTTCACCGTCAT[C/G/T]CCAAATACAGTAAGC	54476
rs574815048	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5646755	GTGTGGTCACTGAAG[C/T]CTCTGTTGTATTAGC	54476
rs574835290	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5710669	AGCCTCCTTCACACT[C/T]CTAGCACCAGTAAGC	54476
rs574852732	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5783577	ACAATAGTCTTGATG[C/T]GGCAATGAGTGTTCC	54476
rs574897588	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5744914	GAGGCAGAGGTTGCA[A/G]TGAGCCAAGATCGCG	54476
rs574905775	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5773830	CCTCAGCCTCCCAAA[C/G]TCCTGGGATAACAGG	54476
rs574918569	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5715858	GCGATTCTCCTGCTT[C/T]AGCCTCCCGAGTAGT	54476
rs574921180	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5758647	CCGCCCTGCTGGGTT[C/T]TGGACTTGTGTGGGA	54476
rs574951469	snp	C/T	0.00597247	0.0543191	intron-variant	RNF216	GRCh38.p7	7:5688027	TGACAATTTTCACTT[C/T]GCTTGATGGAAGGAA	54476
rs574962195	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5763790	GCTGCCCAGGCTGGT[A/T]TGGATATCCCGGTCT	54476
rs574965233	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5640509	CACCTGCTTTCTTTC[C/T]GATCCCCAAACAGAC	54476
rs574978063	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5725070	ACTCAAATACCTTCT[C/T]ACACATGAATTTTCT	54476
rs574997681	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5711265	TGCTCCCACGTAATA[C/T]AGTCAGTTCTCATGA	54476
rs575001652	snp	C/T	1.68795e-05	0.00290507	intron-variant	RNF216	GRCh38.p7	7:5641131	CTCCCTATAAAGCAA[C/T]AGGCAGCCATGTGTC	54476
rs575002836	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5689688	CCAGGCATGGTGGCT[C/T]ACGCCTGTAATCCTA	54476
rs575089022	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620219	GTGACAGATCATGCA[A/C]ATTTTTTTCAGTTTT	54476
rs575093784	in-del	-/AAACAAAACA			intron-variant	RNF216	GRCh38.p7	7:5633575	GGGAGACTCCCTCTC[-/AAACAAAACA]AAACAAAACAAAACA	54476
rs575099250	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5646691	GCGAGACTCCATCTT[-/A]AAAAAAAAAAAAAAG	54476
rs575099917	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5651270	GCTCTGTCGCCCAGG[A/C]TGTAGTGTTGTAGTG	54476
rs575106368	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5693437	CAAAATGTACTGAAA[C/T]TGTTCCCTGCTGATG	54476
rs575128769	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5720107	CACTGGCCTGATTCA[C/T]GCCAAGGCACCACTG	54476
rs575130697	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5743551	ATGCCATTAAGTGAA[A/G]AAAAGCAAGCTGCAA	54476
rs575141728	snp	C/G	0.0023933	0.0345097	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620677	TCAAATGACCCACCC[C/G]TGGGGTTTGGCCTTA	54476
rs575142010	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665234	AATCATCTCTCAAAG[G/T]AAGGAGAACCTTTAC	54476
rs575146637	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5710203	CATCTCTACTAAAAA[C/T]ATAAAAATCAGTCAG	54476
rs575175154	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670262	CATAAACAACCTGGA[C/T]GTGAGACTTTCAGGA	54476
rs575177526	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5775620	CACACCTGTAATCCC[A/G]AAACTTTGAGAGGCC	54476
rs575183911	snp	C/T	5.11854e-05	0.00505866	intron-variant	RNF216	GRCh38.p7	7:5715029	TGTGTCCTATATACA[C/T]GGGACATATTACACA	54476
rs575184395	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5639420	TTCCTTTTTTTTTGA[A/G]AACCCAAAGTGCCGG	54476
rs575192174	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5774058	CCCAACCTGTGAGAA[A/G]AAAAGAATTCTGATG	54476
rs575236407	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5629627	ACGTCAGGAGTTTGA[C/G]ACAGGCCTGGCCAAT	54476
rs575237242	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5623541	CTGGGCTCAACTGAT[C/T]CACCTGCCTCACCCT	54476
rs575246150	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620537	CAGGGTGGGTGCTCA[C/T]GGCAGCCCTGTGGTC	54476
rs575269542	in-del	-/A	0.32153	0.239548	intron-variant	RNF216	GRCh38.p7	7:5690327	GTGAAATTCCATCTC[-/A]AAAAAAAAAAAAAAA	54476
rs575271051	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665823	AGAATCACCGAGACT[A/G]TATCAGCAACGCCTA	54476
rs575278541	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5742586	AGGATGGTGAAAAAT[-/C]TTTTTTTTTTTTTTT	54476
rs575294000	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5763490	TAAAAATTAGCCAGG[C/G]GTGGTGGCAGGCACC	54476
rs575304885	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668545	GGACTTTTAATCTTT[C/T]CCTCCTTGCTAGTGA	54476
rs575323191	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5630017	ACCATCCTGTGAAGA[C/G]GACACTTGGAAAAAG	54476
rs575327606	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5772693	AAGTTATAGATACTA[G/T]CAAAATATACAGATA	54476
rs575354257	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782399	TCAGGAAGTTTAGGT[G/T]TTAGTGAGCAAGTGA	54476
rs575369858	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768546	AGAACATTCACAAAA[A/C]AGACTGTATGCCATG	54476
rs575389465	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5687261	ATAAACTGGGCATGG[G/T]GGCGGGCGCCTGTAA	54476
rs575428929	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674794	TGAGATCAGGAGTTC[A/G]AGACCAGCCTGACCA	54476
rs575439935	in-del	-/AAAAAAA			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666179	TCAAAAAAAAAAAAA[-/AAAAAAA]TCCGAAACCAGTATG	54476
rs575445229	snp	A/G	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754219	GCAGTACAATGGTGC[A/G]ATCATAGCTCACTGC	54476
rs575447032	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5776698	GACGTGTCAGATCTG[C/G]GTTTATCCTTTAAAA	54476
rs575447335	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5771679	TAGCGGGCACCTAGT[A/C]CCAGCTACTCAGGAG	54476
rs575456136	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5698482	GCGGCCTCGATCTTC[C/T]GGGCTCAGGTGATCT	54476
rs575460707	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5709787	AAAGACAGAGTCTTA[C/G]TCTGTTGTCCAGGCT	54476
rs575473241	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5644916	TGCAACCTCCACCTC[C/T]TGGGTTCAAGAGATT	54476
rs575484349	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5771971	GGGCGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC	54476
rs575518043	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5771004	GTAGAGACAGGGTTT[C/G]ACCATGTTGGCCAGG	54476
rs575555107	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5630405	TTTTCCCTCTAGACA[A/G]GGTCTTGCTCAGCCC	54476
rs575558796	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5628662	TGGTAGCTCAGACTA[C/T]AGGCGCCCACCACCA	54476
rs575569793	snp	A/C	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5691915	TCAAGACAAGTAATG[A/C]AAGACAGACCCCAGG	54476
rs575577334	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675829	ATTCTCCTGCCTCAG[C/T]CTCCTGAGTAGCTGG	54476
rs575578589	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5696592	GTGTCCTATGGTCTC[A/G]CTTCGGCCGCTCTTC	54476
rs575581412	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664455	GTGAGAAAGTACTGC[A/T]TATGTTTCAATTAGG	54476
rs575594576	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5728878	CTACAAAGCAGGCAC[C/T]GTGTGCTGTCCTTCA	54476
rs575597865	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5691113	TTTAAGTTCCGACAG[A/C]AGCACACCCATTTCT	54476
rs575608673	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5723767	ACTCTTTGAGTCAAG[C/G]AATTATAGCCCAAAG	54476
rs575618959	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5770241	CCAAGGTGGGCGGAT[A/C]GCCTGAGGTGGGGAG	54476
rs575621769	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5751393	AGTGTGTGCACTAGA[C/G]CCCAAAAGACCAGAC	54476
rs575623411	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5756860	AGGCTGGCCTCGAAA[A/T]CCTAGGCTCAAGTTA	54476
rs575624809	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5748861	ACCATGTTGTTCAAG[C/T]GTAAACTGTATTTGA	54476
rs575628460	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5628141	GCATCCTCACCCTCC[A/G]AAGACAGCCACCCCA	54476
rs575638822	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5772464	CAGGCTGGAGTGCAG[C/T]GGTGCGATCTCGGCT	54476
rs575645361	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5718357	CTGCACTCCAGCCTG[C/G]GTGACAAAGCGAGAC	54476
rs575653997	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679873	GCCTTTCTGCTAAGC[A/G]GCCAGAGTCCCTGGG	54476
rs575658480	snp	A/G	0.00398564	0.0444627	intron-variant	RNF216	GRCh38.p7	7:5751977	CGGATCACGAGGTCA[A/G]GAGTTCAAGACCAGC	54476
rs575667032	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5762843	TTTTTCTTTCTTTTA[A/G]AGATATTTAAAGCAA	54476
rs575678398	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5686645	TTAAATACATGTGAG[C/T]TGGGTTTGGAAGATT	54476
rs575681663	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5695109	ATATAGCCAAGAAGT[G/T]CAATGACTTCAAGCT	54476
rs575696296	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5658621	ATGATCAAGCTACTG[C/T]ACTCCAGTCTGGGTG	54476
rs575713491	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5724246	GAAGGGCAGTCAGGC[C/T]GATGAAGGGACAACA	54476
rs575719013	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5708548	TTCACTTTCAGTACA[A/G]TACTCAATAAATTAC	54476
rs575723947	snp	C/T	0.00279162	0.0372561	intron-variant	RNF216	GRCh38.p7	7:5692502	CCGCGGGGCCCTGAC[C/T]TCTGGTCCAAGGTTT	54476
rs575727346	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5632983	GGAACTGGAAGAGCA[C/T]TTTCTGTTTTTTTTG	54476
rs575756254	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5659251	GAGACACCGGAGATA[A/C]AGCAATAAACAAGTT	54476
rs575760068	snp	A/C	0.00119737	0.0244387	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669343	AGATCTTTAGAAGAC[A/C]AATCTTTGCCACTGG	54476
rs575765771	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5680339	GATCCACTCCCCCAA[A/G]CCCAAGTCTCCTACC	54476
rs575768889	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5654578	TGTAATCCCAGCTAC[C/T]TGGGAGGCTGAGGCA	54476
rs575802821	snp	G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5642319	CCCGGGTTCAAGAGA[G/T]TCTCCCACTTCAGTC	54476
rs575855460	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5766431	GGAGATGGAGTCTGT[C/G]GGAGGTGATTAGAAT	54476
rs575875313	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5628026	ATACAGATCGGCGGG[G/T]TCTGGAGGACACTGC	54476
rs575877093	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663181	TTGTAATTATCTGAT[C/T]ATGTCACATCTTTTC	54476
rs575877968	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5709095	GGACTCATGCTCCAA[C/T]TCCTTCCCTCCCGAG	54476
rs575881031	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5657490	GAGAATAGCTTGAAC[C/G]CAGGAGGTAGTGGTT	54476
rs575905594	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5685634	GGGGCATAGTGGAAA[A/C]GGAAGTAAAACACCA	54476
rs575918137	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5777313	TATGAAGCAGTAAGT[A/G]TTAGGGTGGTTTGTT	54476
rs575922234	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5633660	TGTTTCCTTTCCTTG[A/T]ATTCCTTTGAGCTCA	54476
rs575933253	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5756342	CAGTGTGAAAGCAGA[C/T]TAATACAGTTGCTTT	54476
rs575953059	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736903	CGCCCCGTCCGGGAA[G/T]TGAGGAGCCCCTCCG	54476
rs575984306	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5642441	CTGGTCTGGAACTCC[C/T]GACCTCAGGTGATCC	54476
rs575986371	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5737233	TTACCCCCAACCCAG[C/T]GCTCTCTGAAACATG	54476
rs575988278	in-del	-/TTTT			intron-variant	RNF216	GRCh38.p7	7:5647348	TTTTTTTTTTTTTTT[-/TTTT]GAGATAGGGTCTTGC	54476
rs576012588	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5624869	TTGGGTTTTTGCCAC[A/G]TGCAGCTCCCACACC	54476
rs576016839	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5746833	ATGTGGAATGTTCCA[C/G]ATGAAAAAGAGTGTT	54476
rs576062476	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5708914	CTTCGAGGTGCACTG[C/G]ACTCTGCCTACTGTA	54476
rs576067638	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713561	CACCCCAGGTAAGAG[A/G]CTTCAGAGCCATTCA	54476
rs576073618	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5747351	GTGGGACCAGGGGAA[A/G]GAGAGGGAGTAAAAA	54476
rs576106589	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736242	CCTGCCTCAGCCTGC[C/T]GAGTGCCTGTGATTG	54476
rs576120534	snp	C/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5637210	TGCCTGGGAATGTCT[C/G]TCACACAGGGGCACG	54476
rs576126387	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664617	CAGGACTGGAAATGC[A/G]CATTCTGCCTGTGTC	54476
rs576132463	snp	C/G/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5765700	GTAATCCCAGTACTT[C/G/T]GGGCGGCTGAGGCGG	54476
rs576135016	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5644191	TTCACTTATGTTGGG[A/T]GAGTACCTGAGAGCG	54476
rs576138298	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5707366	TCCTTGGTTAAGTTG[A/T]TCCTAAGTATTCCAA	54476
rs576140174	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5728464	CTACAGTCCCAGCTA[C/T]TCAGGAGGCTGAGAC	54476
rs576148029	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5756136	AGTCTTGAGGTGTCC[A/G]ATGGTTTTATATGCA	54476
rs576171916	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5760924	AATGGTACAAAATAG[A/G]TTCATTTCAAAAGAT	54476
rs576200991	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5726923	GGAGAAGGGGTACCT[A/G]ATTTGAAACGGAAGG	54476
rs576204232	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5732137	TATTACAGAGGGCGA[C/T]AAGAATTCAGAGTAC	54476
rs576204483	snp	A/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5690188	AAAAATTAGCCAGGC[A/T]TGGTGGTGCACACCT	54476
rs576220986	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643693	AAAATGCACATAAAA[C/T]TGACTTTTTAAACCA	54476
rs576222869	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5637859	TTACGCATTTCTTTT[C/T]CTTTAAGATCAAGTC	54476
rs576261723	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5695273	TACAAAACCACCTGC[A/G]CAGACCCAGTGCAGC	54476
rs576262554	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713483	CTCCAGACCTTTCCT[C/T]CCCCTCAGTTTCAGA	54476
rs576269884	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5627016	GGACTGCACAACCAC[C/T]ACTCTGCCTCACCTC	54476
rs576272053	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5701710	TAACCACTGAGCTAT[A/C]CCGTTTCCCTCACTG	54476
rs576279628	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5684562	ATGTTCCCTGGGGTT[A/G]CTGGAAATCAAGTCT	54476
rs576281004	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5653526	GAAAGGCGTGAACCC[A/G]GGAGGCGGAGCTTGC	54476
rs576305460	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621996	CTCCCTAAGGAGGCC[C/T]ACTCCTCCCCCAGAA	54476
rs576308655	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5647214	GAATTCCCTACACTG[C/T]CATGTTTTTGTAATG	54476
rs576319918	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754606	AGGCACAGGAGTCAA[A/G]AGAGAAAATGTACAC	54476
rs576329471	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5685880	TGTGAATTCTTTATA[C/T]TTGGAGCACTATAAT	54476
rs576336329	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5686342	AAGAGCCCTTACCTG[C/T]TGCGGCCTCATTTGC	54476
rs576339065	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5636809	AGCAAATCTAGAAAC[C/T]TTCTCAGGTTAGAAG	54476
rs576373453	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5699019	CTAACACTGAAGACA[C/G]CTAGAGTTTTTGACT	54476
rs576379961	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672900	GAGCCCTACTGGATT[C/T]TATCGTTTGACCAAG	54476
rs576395643	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667856	CTGGACTTAAAGTCA[A/C]TGGATCAGATTGGGG	54476
rs576398409	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5699998	AGAAATTCCACCCAA[C/G]AGCAGCTTCAGCTTA	54476
rs576428558	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5723033	CAGTAAGCTTTGAAG[C/T]CAGATTCCCAGCTGG	54476
rs576433740	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668318	AAGCTCCGCCTCCCA[A/G]GTTCACACCATTCTC	54476
rs576439106	snp	C/G	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5710545	AGGCTGTGCAGTGCT[C/G]TACATTTCTCACCTG	54476
rs576453005	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622378	CCCTCACAGCTGTGG[C/T]AGTGCCTCTGCGGGC	54476
rs576477731	snp	A/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5706715	TCCCAAAGGATTTCA[A/T]TTCCTTTCCACCGGC	54476
rs576500330	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679015	CACAAGTGTAGAATA[C/T]TTTAAAAGTTATTGA	54476
rs576519207	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5689540	CCTAGGCTTGTAGTC[A/G]AGTAGTTTTCCTTTT	54476
rs576532441	in-del	-/C	0.0111196	0.0737302	intron-variant	RNF216	GRCh38.p7	7:5735536	ACTGAAAACCAGTAA[-/C]ACGGTAGATGAGTTA	54476
rs576538773	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5653366	GAGGCCGAGGTGGGC[A/G]GATCACGAGGTCATG	54476
rs576555030	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5721718	CATCGGTTTTTAATT[A/T]TAGCCATTCTGGTGG	54476
rs576555681	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5770758	AGACAATATTGTATT[A/G]ACAAAAGAAAAACAG	54476
rs576577510	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5621070	ATAGCAGCAGGCTGC[C/G]CCCAAGCCCGGCCTC	54476
rs576592758	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652139	ATTAAAACGCGTTAC[G/T]TGCTTATTTAGAAAA	54476
rs576598185	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5770815	TTCTTTTTTTTTTTT[G/T]CTTTCCCCCCGAAAC	54476
rs576605934	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5750447	TATCTTTGGTAGAAA[C/T]GGGAGTGACTTAGAG	54476
rs576653131	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5773201	ACAGCTCTGGTATCA[A/T]ATTTGAACTGCATCT	54476
rs576666114	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5683847	AGAATTTACAGCCTA[A/G]TTGCTATGGCCATCA	54476
rs576682843	snp	C/T	8.03374e-05	0.00633737	intron-variant, nc-transcript-variant	RNF216, MIR6874	GRCh38.p7	7:5711885	TTCAAACATTAAAGC[C/T]TGATCTGGTTCCAGC	54476
rs576691905	snp	G/T	0	0	intron-variant	RNF216	GRCh38.p7	7:5779925	CGCCACTGTTTCCGA[G/T]GGACGCGGATATGCT	54476
rs576698804	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5755193	AAAGGAAGAAGGAAG[A/G]AAGGAAGGGAGGGAA	54476
rs576718096	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5705645	CTGGGCACGGTGGCT[C/T]ACCCTGTAATCCCAG	54476
rs576748263	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5764280	ACTATACAGGCTATT[A/G]GACAGTAGTAAAAAT	54476
rs576834725	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5774612	CTTACATTACAAGGC[C/T]ATGTTGAAAAATGAG	54476
rs576847377	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682288	ACCTCAGAGGCTACT[C/T]GACCAGGTTACCCTC	54476
rs576851967	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5694177	TCTTACTAAAAAGGG[C/G]ATTTTGTAAACTTTC	54476
rs576857469	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754224	ACAATGGTGCGATCA[C/T]AGCTCACTGCAGCTT	54476
rs576871998	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5645869	TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC	54476
rs576872801	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5735392	CCCAAGAACTTAACA[G/T]ATCAGAACAATCAAA	54476
rs576891179	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666955	GAGTAGCTGTGACCA[C/G]AGGCACATGCCACCA	54476
rs576919684	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5702234	GGGAGTGGGAGTGGC[A/C]GCATAGTCCATGTTC	54476
rs576979327	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671656	AAAAATACAAAAAAA[C/T]CAGCTGGGCGCGGTG	54476
rs576987144	snp	C/G/T			intron-variant	RNF216	GRCh38.p7	7:5642152	TAGTACATCCGTTTA[C/G/T]GATTTTAGTTACTCA	54476
rs576999005	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5777152	AGCAGTCTTTGACAA[C/G]GCATGTGAACGAAGA	54476
rs577001699	snp	C/T	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5744840	AGCTGGGAGTGGTAG[C/T]GCATGCCTGTAATCC	54476
rs577032486	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5656874	TTTCTCAAGAACCAG[C/T]AGACAAATGTATCCG	54476
rs577035641	snp	A/C/T	0.000335589	0.0129492	intron-variant	RNF216	GRCh38.p7	7:5741863	TCTTTCCTATGCCTA[A/C/T]CCCTCCTTATGTACT	54476
rs577054061	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5711252	ACCTAGACAGCTCTG[C/T]TCCCACGTAATATAG	54476
rs577064895	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5744458	AGGAGGAAGGAAAAC[A/C]AGGGAGGGAAGGGAA	54476
rs577068850	snp	A/G	0.0023933	0.0345097	intron-variant	RNF216	GRCh38.p7	7:5659896	CACATTTTCTGATAT[A/G]GCTTCAGAAAGGGAC	54476
rs577071019	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5640382	GCTAGTGTGACCTGG[A/G]AAACATAGCCCCTAC	54476
rs577080987	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5660403	TTCAAGTGATTCTCC[C/T]ACCTCAGCCTCTCGA	54476
rs577086975	snp	C/G	0.00358779	0.0422022	intron-variant	RNF216	GRCh38.p7	7:5763423	ATCATTTGAGGTCAG[C/G]AGTTTGATACTAGCC	54476
rs577096452	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5635981	GAAAACAATTCTCTG[C/T]AGTTTCTCGTAGCCA	54476
rs577103173	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5630821	CACAGCTCCCTGAGT[A/C]AGGCACTATGAACTG	54476
rs577104284	snp	C/T	0.000747775	0.0193217	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739561	AGGTCTTGAGAGATC[C/T]GGTTCTCTGTCCCCA	54476
rs577106987	snp	C/G	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781262	CAGCAGACCCGAGGG[C/G]CCGGCCCGCGAAACT	54476
rs577130104	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5650113	CTCTATGAAGTTCTG[C/G]TGGTCTGGAGGTCAG	54476
rs577154563	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620153	CTATTTTTACTACCA[C/G]AAGGTAAAGAAAAAG	54476
rs577156237	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753823	AACACGGTGAAACAC[C/T]GTCTCTACTAAAAAT	54476
rs577158668	snp	A/G	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5716279	CTTTGGGAGGTTGAG[A/G]TGGGTGGATCACCTG	54476
rs577172165	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF216	GRCh38.p7	7:5783066	GCCGGGCATGGTGGT[A/G]CGCACCTATAGTCCC	54476
rs577177363	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5644640	CTCCTGAGTAGCTGG[A/T]AATACAGGCTTACAC	54476
rs577179009	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666503	CTGTAAGGTGGAGAG[A/G]AGGGTTGGGTTTGCA	54476
rs577187325	snp	C/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739425	AATACAAGACAGATG[C/G]CAAAAAGTATAATAA	54476
rs577199238	snp	A/C	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5650786	TAATCCAGATAACCT[A/C]CCCATCTCAAGGTCC	54476
rs577214940	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5689773	AGCCTGGCCTGCGTG[A/G]CAAAATTCCGTCTCT	54476
rs577258444	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5742731	CTCCCGAGTAGCTGG[A/G]ATTATAGGCGCACAC	54476
rs577293758	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5737926	AACCCTGTCTCTACT[A/G]AAAATACAAAAATTA	54476
rs577294578	snp	A/G	0.00676609	0.0577691	intron-variant	RNF216	GRCh38.p7	7:5701568	GAGGTAGGTGCAACC[A/G]TTCTTATTGTACACG	54476
rs577327532	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5748517	AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCG	54476
rs577331139	snp	A/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5733668	AAACATTAACCAAAA[A/T]AAAAAAAAAAAGGAA	54476
rs577345694	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5720692	GCCACTGGTTTAGAA[A/G]ATACTTATTAAACAA	54476
rs577422328	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5655235	TCTGCTCACCCTCTA[C/T]GTCACAGTGCTTCTT	54476
rs577429814	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5729846	ACCAATCTTACAGCC[A/G]TCTTCTTTCCATACC	54476
rs577432927	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5639993	CTCGATCTCCTGACC[C/T]TGTGATCCACCCGCC	54476
rs577441369	snp	A/G	0.00716266	0.059414	intron-variant	RNF216	GRCh38.p7	7:5633997	ATGAGTGATTAAAAA[A/G]GGGAAAAGATTCAAT	54476
rs577445832	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5698426	ACACATACACACACA[C/T]GCATGCATGCTGGAG	54476
rs577446897	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5692586	CCGTGCAGAAGGCGA[A/G]CGAGGAGAAAGGCAG	54476
rs577475175	in-del	-/AAAT	0.369958	0.21934	intron-variant	RNF216	GRCh38.p7	7:5734825	CAAAACTCTCTCTCA[-/AAAT]AAATAAATAAATAAA	54476
rs577481080	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5704798	GCCGTCACTGCCTCA[G/T]GTCCCCATATAACAT	54476
rs577486602	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5655584	GCACTCCAGCCTGGG[C/G]AACAGAGCAAGACTC	54476
rs577518787	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5748422	TCACCACCATGCCCA[A/G]CTAATTTTTGTATTT	54476
rs577524722	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5629970	ATTCTGGAGTCAAGT[C/T]CCTCAGGAAACATTC	54476
rs577536036	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5644250	GTTTAACTTATTGGG[A/G]AAAGCCAACTGTTAA	54476
rs577551076	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5644512	ATATTGTTTGCCCAT[-/T]TTTTTTTTTTTGAGA	54476
rs577559434	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5639645	TTTATATTTTTATTA[A/G]AGACAGGTTTCACCA	54476
rs577564480	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675267	CCCTCTGCACACACG[C/G]TAGGTTCTGCACAGA	54476
rs577579395	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5702591	CTTTAAAAGAATCTA[A/G]CAAACACATCTACTC	54476
rs577593809	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5688067	GCAAATGGAACCGAA[A/G]AGGTAATTAGAGCAG	54476
rs577625987	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5772417	AAATTACTATAAACA[C/G]AAGATTTAAATGTGC	54476
rs577639564	snp	C/T	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5660490	AGAGACAGGGTTTCA[C/T]CATGTCGGCCAGGAT	54476
rs577643501	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5704378	GCTTGTGGCTCATGT[C/G]TTAAATATCAGGAAT	54476
rs577660457	snp	C/T	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5624589	GGACAAATGTCCAGT[C/T]GGGCCCTGCTTAGCC	54476
rs577676858	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668093	GGTTGACAATACCCC[C/T]TTGTGGATATCAGAC	54476
rs577703756	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767907	CCCAGCCTGTTGAGA[A/G]AGATTAAAGGTCAAG	54476
rs577711677	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681600	CCACTGACCACACTG[A/T]CAACCTTTCAATGTT	54476
rs577719491	snp	G/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5691815	AACATATTTTCGATG[G/T]TTTAAATAACTTCTC	54476
rs577743536	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5709263	TGAATATTAGATATA[C/T]GTTCCAGTCTTCTTT	54476
rs577747907	in-del	-/ACGA			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665078	GCTGCGATTACAGGC[-/ACGA]ACCACCGCACCCAGC	54476
rs577772771	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5649885	GAATGATTTGGAAAA[C/T]GCTTTTCCTGTCTGT	54476
rs577804751	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5709659	GGTGTTCCTATTTGG[A/G]ATCTTAAGAGCCCCT	54476
rs577813327	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5719503	GTCAGAGACTACAGG[A/G]GTCGGGTTAAGAGAG	54476
rs577818828	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5704289	TTCCTGAAAAGCCAA[A/C]TGGAATTTATATTAC	54476
rs577840066	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5775761	GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	54476
rs577871366	in-del	-/A			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669883	GCAAGACTCCATCTC[-/A]AAAAAAAAAGAAAGT	54476
rs577874982	snp	C/T	0.00199481	0.0315187	intron-variant	RNF216	GRCh38.p7	7:5776301	GTAATAAAGAGACTA[C/T]AGCCGGGCACGGTGG	54476
rs577896555	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5627994	CACCTGCATAGGAGC[A/G]CGAGCCCAGGTTTCT	54476
rs577906543	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5757524	CACTAGGTACAGAAT[C/T]GTAGATGAGTAGGTA	54476
rs577918277	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5708357	ACTATTTTTGTGTTA[C/T]TTTTCCCTTCGGCTG	54476
rs577919729	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736881	AGGAGCCCCTCCGCC[C/T]GGCAGCCGCCCCGTC	54476
rs577920722	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5702061	GGCGACATCTGAGGC[A/C]CCAGGTCGCTGCCGG	54476
rs577935356	snp	C/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5686617	CTTAGAACTGCACTT[C/G]TCAACTATTTCTTTA	54476
rs577944506	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5633168	AGTTTTAGTAGAGAC[A/G]GGGTTTCACCATATT	54476
rs577955018	in-del	-/AAACA	0.00517822	0.0506191	intron-variant	RNF216	GRCh38.p7	7:5633574	GGGAGACTCCCTCTC[-/AAACA]AAACAAAACAAAACA	54476
rs577997425	snp	A/G	0.00159617	0.0282053	intron-variant	RNF216	GRCh38.p7	7:5732672	CATTTGGAGGCACAG[A/G]AAATGAAGGACAAAG	54476
rs578000805	snp	A/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5658558	AGCTACTTGGGAGGC[A/T]GAGGGGGAGGATTTC	54476
rs578021496	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5766992	TGCTACTATGTATGA[A/G]CCATTTTTCTTATCA	54476
rs578027149	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	RNF216	GRCh38.p7	7:5782275	AAAATCACTTGAACC[C/T]GGGAGGCGGAGGTTG	54476
rs578027882	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5758595	ATGTGAGATGTGGAG[A/T]CAAAGGAGGTTATTT	54476
rs578039598	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5732934	GCTGACCACGTGTGA[A/G]TGAAAGGTCTAAGTT	54476
rs578055600	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669241	TCTGATTCCGACACA[C/T]AGTAAAGTTGAGAAG	54476
rs578061464	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5659084	GATGTAGGACACTAG[C/T]GAGATTGGTGGAAAC	54476
rs578065444	snp	A/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5756759	TATCCCAAGTACCTG[A/G]GACCTGGTAAACCCA	54476
rs578071562	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5691377	GTTCTGGCTGGATTG[A/C]TCCTGGCTGGATTGC	54476
rs578078329	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5697186	GAGTAAAGTTCTCCC[A/C]ATCTCCGCCAATAAG	54476
rs578101550	snp	G/T	0	0	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663793	GTCCCAGCTACTCAG[G/T]AGGCTGAGACAGAAG	54476
rs578120027	snp	C/G	0.000798403	0.0199641	intron-variant	RNF216	GRCh38.p7	7:5761983	CACTTCCAGGTATAT[C/G]AGCTAAAGAAACCTC	54476
rs578129220	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5734553	ACACAATAAAGAATA[C/T]GTGGAAAGGCTTCAG	54476
rs578132752	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713053	ATCTTTGATATCACT[A/G]AAGGACCTCTATTAG	54476
rs578147627	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5762353	CATGGTGAAACCCCA[C/T]CTCTATTAAAAACAC	54476
rs578152371	in-del	-/TTGCTCTTAATAATATGATACGAA	0.00119737	0.0244387	intron-variant	RNF216	GRCh38.p7	7:5688819	TTATTAGTGAAAGAG[-/TTGCTCTTAATAATATGATACGAA]TTCCCAAATGATGAT	54476
rs578166237	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5771157	TAGCATTGCAGAGCA[A/G]TGGAAAACATGACCT	54476
rs578178552	snp	A/G	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5736584	GCCTGGCCGCCCATC[A/G]TCTGGGATATGAGGA	54476
rs578180480	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5692341	TTATTTGCTGATTTC[A/G]CAACCCAAAGCAGAC	54476
rs578182460	snp	A/C	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5746736	GCCTTTTCATGTATA[A/C]AACTTCTGGCTCCAG	54476
rs578186796	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5643140	GCCTGCAACTCAACA[C/T]TGCTGAAATGTTAAA	54476
rs578207667	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713241	GAGCTGAGTGGTGGG[A/G]AGGGGCAGGGACTCA	54476
rs578209717	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5632828	CTACTCCAGAAGGTG[C/T]ACCTATGGATCACAG	54476
rs578223730	snp	C/T	0.000399281	0.0141238	intron-variant	RNF216	GRCh38.p7	7:5638190	ACTGTTTGTTTTCGA[C/T]GTGAAAATCTTCCTG	54476
rs578234841	snp	A/G	1.64754e-05	0.00287009	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741106	TCATCATCACTTGCT[A/G]ACTGCTGGTCTTCAA	54476
rs730882248	snp	A/G			synonymous-codon, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711761	TCCTCACTGCCGAAA[A/G]GTAGGGAGGCACATT	54476
rs745309786	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5697194	TTCTCCCCATCTCCG[C/T]CAATAAGACCCCACC	54476
rs745354177	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5759557	TAACGCATGTGTTGA[C/T]TGTTTATGTTATCAG	54476
rs745363798	in-del	-/AAGG			intron-variant	RNF216	GRCh38.p7	7:5755243	GGGAAGGATGAAAGG[-/AAGG]AAGGAAGGAAGGAAG	54476
rs745365465	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5769242	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	54476
rs745394380	in-del	-/G			intron-variant	RNF216	GRCh38.p7	7:5697170	TCATTCTCTGGGCCT[-/G]GAGTAAAGTTCTCCC	54476
rs745396983	snp	A/C			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767423	GACTTAAGGGACAAA[A/C]TTCCAGCAAGGAAGA	54476
rs745414361	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5653525	AGAAAGGCGTGAACC[C/T]GGGAGGCGGAGCTTG	54476
rs745418912	snp	C/T	2.50881e-05	0.00354167	intron-variant, nc-transcript-variant	RNF216, MIR6874	GRCh38.p7	7:5711879	CATTACTTCAAACAT[C/T]AAAGCCTGATCTGGT	54476
rs745439485	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5770967	CATGCACCACCACGC[C/T]CGGCTAATTTTTGTA	54476
rs745463946	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5647828	TTATAATACTACAAA[C/T]CTATATTGGAGCCCT	54476
rs745469260	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680891	TTTCTGTTCCGCCTC[C/T]AAAATGCACCTCACA	54476
rs745489441	snp	C/T	1.64841e-05	0.00287085	missense	RNF216	GRCh38.p7	7:5641176	TCGGTCCAGAGAGAG[C/T]ATCTTGAACACTCCT	54476
rs745504258	snp	C/G	3.29451e-05	0.00405851	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741574	TCTGTTTGGCCACTT[C/G]GCTTAGTGAATTCAG	54476
rs745513144	snp	C/T	3.52181e-05	0.00419617	intron-variant	RNF216	GRCh38.p7	7:5730839	AAACAAATGATGTTA[C/T]TTTCATACTGCTTCC	54476
rs745522866	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5696247	AAAGCAGGGCTCTCA[A/G]CAGCTGGGAAAACAT	54476
rs745532290	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5732993	TGGTTCTCTAATGAA[C/T]AGGCTTCCTGCTTAA	54476
rs745548639	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5637425	TTTAGGGGTCTCTTA[A/T]CCCAGCTTCCCACCC	54476
rs745558380	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663048	CACCTACTCACCAGT[C/T]CTCCTTTCAAATACC	54476
rs745559221	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5634610	TTCACGGGCTCAGGG[A/C]TGGCCCTGGCTTCTG	54476
rs745561818	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5626295	TAACTCAAGAGGGTT[C/G]GGTGGGCAGTTTGAA	54476
rs745584197	snp	C/T	3.29457e-05	0.00405854	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741495	GATGACTTTCTGCTC[C/T]GATCTGGGGTTGACA	54476
rs745613035	snp	C/T	1.64773e-05	0.00287026	missense	RNF216	GRCh38.p7	7:5729440	AGAGTACCTTTCGGG[C/T]GATTGCATAGTGTCC	54476
rs745613441	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5716211	ACCCATTCTTAATAC[C/G]ACATTAGAAAGGGTC	54476
rs745632553	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5745221	CCAACTAAGAGGTCA[A/T]GGAAGAAAAACCACA	54476
rs745635533	snp	A/T	4.94719e-05	0.00497328	utr-variant-5-prime	RNF216	GRCh38.p7	7:5761107	ATGGGACTGCTAATA[A/T]CTAAACATGGTGACC	54476
rs745646917	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5738733	AAAAAAAAAAAAAAA[-/T]GCTTCCATGTATTTC	54476
rs745666494	in-del	-/AAC			intron-variant	RNF216	GRCh38.p7	7:5638410	CTGTCTCCTGCGGAT[-/AAC]CTTTTCTAATTAAGA	54476
rs745671649	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5758734	AATGCATGTACCCCC[A/G]TAGTATCTTGGGAAT	54476
rs745680393	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5682640	TTGAACTCCTGACCT[C/T]AAATGATCCACCCAC	54476
rs745682845	snp	A/G			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620930	CTGGGGAAGCACAGG[A/G]AGCATATTTAAGGTA	54476
rs745716911	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5706658	ATCTTGTGGCTACTG[G/T]GAATAATGCTGCAAT	54476
rs745745214	snp	A/G	3.29755e-05	0.00406038	missense	RNF216	GRCh38.p7	7:5623003	GCCCCATGTTGAGTG[A/G]GAAGTTGTTGAACAC	54476
rs745760717	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5720796	AGGCTGAGGGAGGAG[A/G]TAAAATAGATACACT	54476
rs745806378	snp	C/T	2.9271e-05	0.00382553	intron-variant, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711722	CAGCCCATAATACCA[C/T]AATTCAATATACATC	54476
rs745813947	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5719130	GCATGCCTGTAACCC[C/T]AACAATTTGGGCGGC	54476
rs745831843	snp	A/G/T			intron-variant	RNF216	GRCh38.p7	7:5740276	GGACTACAGGCGCCC[A/G/T]CCACCACGCCCGGCT	54476
rs745843457	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5657260	TTCAGCTCTCTGTTC[C/T]GTCACCTCAAAAAAT	54476
rs745849722	snp	A/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681943	TCTAAAGAATGCTAC[A/T]AAGATGACCATCTCC	54476
rs745863156	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669847	CATCGAGCTGAGATC[A/G]CACCACTGCACTCCA	54476
rs745892103	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5710458	TAAGCACTTTCACTG[A/G]CAGACCTTCTTTGAA	54476
rs745898861	snp	A/C	1.67385e-05	0.00289292	intron-variant	RNF216	GRCh38.p7	7:5715224	CACACATGAAATGTC[A/C]TGCACTTAAGGAGAG	54476
rs745900637	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5749446	GTGAGCCACCACGTC[A/G]GGCCTATATGGATGT	54476
rs745910067	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5630671	GTGCAGGGATTACAG[A/G]TGTGAGCCACTGCAC	54476
rs745961646	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677224	AGAGACTGCTCAGCA[C/T]GTGCTTCTGCAACAT	54476
rs745978079	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666340	GAGAGGGGGAAATAG[C/T]TCACGATTATAAACT	54476
rs745980631	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5701313	AGTGATGAGTCATCT[C/T]CTGTTCCCTGATGGG	54476
rs745987556	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5748410	GATTATAGGTGCTCA[C/G]CACCATGCCCAGCTA	54476
rs745990015	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5739893	CTGTGATCCCAGCTA[A/C]TCGGGAGGCAGAGAC	54476
rs746001614	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5631762	CAGCTAAAATCAGCC[A/G]TAATTCCTCACCAGA	54476
rs746003951	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5724447	TGTATGGCTATGTAC[A/G]AGGATGCCTGTTCTG	54476
rs746019517	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5757766	CACAAGGGAATCTTT[C/T]TGGAGTGATAGAAAA	54476
rs746022217	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5640550	TAATTTCCTTGCCAG[C/G]CTTGCTCCTCCTCTA	54476
rs746030717	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5709969	ATGTTGCTCAGGCTG[A/G]TCTCGGACTCCTAGT	54476
rs746067237	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5685902	CACTATAATGCATTT[C/T]TATGTACTGACCTTG	54476
rs746080152	snp	A/G	1.76275e-05	0.00296874	missense	RNF216	GRCh38.p7	7:5623149	TCCACAGGCTTCTCC[A/G]GCGGGGGTCCAATGC	54476
rs746089255	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5709483	GGTCTGGAGCTTTCT[A/C]TTCTGTCATCTTGAC	54476
rs746119138	snp	A/C/G	3.29643e-05	0.00405971	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5729557	AGCGCTGGTCAAGAG[A/C/G]GGTCAATTTAGAATA	54476
rs746123754	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5748934	CTTCTCTGTGTCTCC[A/G]TGTCTATATATGCGT	54476
rs746126716	in-del	-/CA			intron-variant	RNF216	GRCh38.p7	7:5773718	GACGACACATGCGTG[-/CA]CCACCATGCTGGTTA	54476
rs746130603	snp	A/C/G	0.000131778	0.00811628	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741290	GGTTTGTTATTTCAC[A/C/G]GGGCTGTTGGTTCAG	54476
rs746150199	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5705033	TTTAAACTTAGCATG[C/G]CCCAGCATTTCTAAG	54476
rs746160531	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5658642	AGTCTGGGTGACAGA[A/G]AGAGACTGTCTCAAA	54476
rs746163899	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5728058	TCAGCACATTGGCAA[-/C]CAACGTTTCCCAGAC	54476
rs746167837	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5694233	CTTTATTTGCTGGAA[C/G]AGTTTTCAAACAAGT	54476
rs746176452	snp	G/T			missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5729574	GTCAATTTAGAATAG[G/T]CAAAAAAGTCTATTT	54476
rs746212215	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5715950	GTTTCACCACGTTGA[A/C]CAGGCTGGTCTCAAA	54476
rs746215892	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5624249	AGCCTGCTGCTGGCC[A/T]GTGGGGCCTGGGCTG	54476
rs746235007	snp	A/G	1.65116e-05	0.00287324	missense, upstream-variant-2KB	RNF216	GRCh38.p7	7:5752956	CAGATATGGTGATGG[A/G]CCCATCTCGGAGATT	54476
rs746256708	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5778084	TTTTCATACGGCATT[G/T]GAGTTATTTCTTTTA	54476
rs746268092	in-del	-/AAAC			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675643	AGACCCTCTCAAAAC[-/AAAC]AAACAAACAAACAAA	54476
rs746276970	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5647385	GTTGTTCAGGCTGGA[A/G]TACACTTGTACAATC	54476
rs746280202	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5625093	CCTGGCTGGCTGCAG[A/G]GCCAAGGGGCTAAGG	54476
rs746295834	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5778018	GTGACCAAAGGACAT[A/G]CTTCTGCTTCTAGCC	54476
rs746303360	snp	C/T	1.7224e-05	0.00293457	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5711946	TTTGAGCTGGACATT[C/T]ACATCCCCTTTATAC	54476
rs746311396	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5643748	ATTTTGAGTATTCAC[C/G]ATGTTATACAATCAA	54476
rs746317006	in-del	-/ACC			intron-variant	RNF216	GRCh38.p7	7:5739231	TATTACATATATTTT[-/ACC]ACCACCACCACCACC	54476
rs746326036	snp	C/T			downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619586	CAACAGCGAGGGTAG[C/T]AGGGCCCTGGCACTG	54476
rs746356228	snp	C/T	3.34823e-05	0.00409146	intron-variant	RNF216	GRCh38.p7	7:5721218	CAGACAACTATGTGT[C/T]AGGAACCTGGGCCAG	54476
rs746357774	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5630724	GCGCCAAGCACAGTG[A/G]CAACAACAGTAGTTA	54476
rs746386979	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5743829	GCCAAGCTGGAAATA[C/T]CCTGGACCTCCCAGG	54476
rs746398799	in-del	-/TTTT			intron-variant	RNF216	GRCh38.p7	7:5659857	GCAGCACACCTGTAC[-/TTTT]TTTGTTAAGAAGAAG	54476
rs746410563	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767523	CCACATACATGCAGG[A/G]CTAGACTCCCCAAAA	54476
rs746411828	snp	C/G	1.64857e-05	0.00287099	missense	RNF216	GRCh38.p7	7:5721144	CTTATTTTCAAGAAA[C/G]AACATCCTCTTTTCT	54476
rs746418588	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670914	AGGACTCAAGGTCTT[C/T]CCAAGACGAACCACC	54476
rs746457488	snp	C/G/T	9.90633e-05	0.00703729	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712682	CACAATGGGGAAGAG[C/G/T]TGGCAGATGGCACGC	54476
rs746460940	snp	C/T	1.64727e-05	0.00286986	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741467	TGTAAAGAAGGCTAC[C/T]TTCTTCCAAGATGAT	54476
rs746461058	snp	C/T	1.91305e-05	0.00309272	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5730727	TGCCTTTGTCTCATC[C/T]TGGCTGGCCAGCAGA	54476
rs746469731	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5722938	TTGGGAAGTGGACTC[C/T]GTCTTAAAATTAAAA	54476
rs746490837	in-del	-/AAA			intron-variant	RNF216	GRCh38.p7	7:5654687	GCCAGACTCCGCCTC[-/AAA]AAAAAAAAAAAAAAA	54476
rs746491479	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5751725	TCTTTGTCTATAAAG[C/T]CAACCACTTCTCCTC	54476
rs746513678	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5642682	TGAGGTTTCACCATG[C/T]TGGCCAGGCTGGTCT	54476
rs746521061	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5732087	AACACAACGCCTGAG[G/T]CCCAAAGAGAGGAAA	54476
rs746531633	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5644511	GATATTGTTTGCCCA[-/T]TTTTTTTTTTTTGAG	54476
rs746536249	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5770932	CCTGCTTCAGCCTCC[A/G]GAGTTGCTGGAATTA	54476
rs746545445	in-del	-/G			intron-variant	RNF216	GRCh38.p7	7:5636712	GGGAACGGGACAAAC[-/G]GAACAGAATCTCCGG	54476
rs746570618	snp	A/G	1.89209e-05	0.00307573	intron-variant	RNF216	GRCh38.p7	7:5624157	GAGAAGGATGAACCT[A/G]TAGCTTCATGCAGTG	54476
rs746583340	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5742776	AATTTTTCTATTTTT[C/G]TTAGAGACAGGGTTT	54476
rs746583540	snp	C/G			missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752850	AGAAAACTCACTTCT[C/G]TCAGGATGACATCAT	54476
rs746601189	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5776620	AAAAAAAAAAGACTA[C/T]AGGGGAAGGGCAGGT	54476
rs746603898	snp	A/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666221	TCCTACTAAGGACTA[A/T]GGGTCCTGCTCTGCA	54476
rs746606929	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5638106	AGACGTCTGGATGCT[A/C]CATCCAGACATCATT	54476
rs746630882	in-del	-/ACTGCACCACTGC			intron-variant	RNF216	GRCh38.p7	7:5725802	TCGCAGTGAGCCGAG[-/ACTGCACCACTGC]ACTGCACCACTGCAC	54476
rs746637942	snp	G/T	4.94597e-05	0.00497266	utr-variant-5-prime	RNF216	GRCh38.p7	7:5761094	CAGACATGCATATAT[G/T]GGACTGCTAATATCT	54476
rs746645455	snp	C/T	6.71513e-05	0.00579406	synonymous-codon, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712831	GGTTGGGAACGAACA[C/T]GTGCAGCTGCCTTCC	54476
rs746652973	snp	C/G	1.64735e-05	0.00286993	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741400	TTTGATAACAGCTCT[C/G]TCTCTGAGTCTTCGG	54476
rs746672320	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5721979	TCACGCTGGAGTGCA[C/G]TGGCACATTCACAGA	54476
rs746682653	snp	G/T	1.65658e-05	0.00287795	missense, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712775	TTTCGCTCATAGTAC[G/T]TATACAGGATGGTCT	54476
rs746696722	snp	A/G	1.66604e-05	0.00288616	intron-variant	RNF216	GRCh38.p7	7:5725455	TAAAAATTGAGAAAA[A/G]GAAAGGTTCCTTCTG	54476
rs746722830	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5626412	CTAAGAAAAAAGACT[-/A]AAAAAAAAAAAAAAG	54476
rs746725067	snp	A/G	1.64773e-05	0.00287026	synonymous-codon	RNF216	GRCh38.p7	7:5761013	CTTACCTTGTCCCCG[A/G]TGGCAGTGAAAGTTG	54476
rs746737605	snp	C/T	1.64822e-05	0.00287068	synonymous-codon	RNF216	GRCh38.p7	7:5725370	CTGGTTCATTTGTTT[C/T]CTCTTCTTCCTTTTT	54476
rs746760196	snp	A/G			upstream-variant-2KB	RNF216	GRCh38.p7	7:5782388	TGTTCCTGGCCTCAG[A/G]AAGTTTAGGTTTTAG	54476
rs746803970	snp	A/G			utr-variant-5-prime, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781580	CAGGCAGGTTCGGCG[A/G]CCTTCGCTACCGCGC	54476
rs746828427	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5708534	CAATCATTCTCTTTT[G/T]CACTTTCAGTACAGT	54476
rs746830827	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5697362	AGAAATGCTCAATAC[A/G]TATCTGCTGAACGAA	54476
rs746832844	in-del	-/CC			intron-variant	RNF216	GRCh38.p7	7:5705163	TCCCTGTGTTACTGA[-/CC]CCCGGATCACTGATC	54476
rs746865554	snp	C/T	1.65064e-05	0.00287279	missense	RNF216	GRCh38.p7	7:5622939	ATGGGACCGAAGTCA[C/T]AGTTGACCCGCACGT	54476
rs746894123	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679211	GTGGTGGTGCGGTGG[C/T]GGGGGGGCGGTGCAC	54476
rs746913911	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5717302	AGGTTGCAGTGAGCC[A/G]AAATCGCACCATTGC	54476
rs746915378	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5693011	ATTGTGGGCATATTG[C/T]ACCCATTGTTCTACG	54476
rs746929773	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5682960	CAACTCAGGAGCAAG[C/G]ATAGGTAAACCAACA	54476
rs746938392	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5746231	AAGGTTAGGCTGCAC[C/T]GTGAGAGAGCATTTG	54476
rs746947360	snp	C/T			missense	RNF216	GRCh38.p7	7:5623144	CCTTCTCCACAGGCT[C/T]CTCCAGCGGGGGTCC	54476
rs746969171	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5648013	CCAGACACTGCATAG[C/T]TCTGGGTGTTTTGTA	54476
rs746989710	snp	G/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673296	TGCTTACGGTAATTA[G/T]CGTGGCCCTGTCAGT	54476
rs746996088	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5727987	ATTTTCCAAACTTTC[C/T]AGTCCATTCAACCTC	54476
rs747005540	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5769358	CTTGACCCTGTGATC[C/T]GCTGGCCTTGGCCTC	54476
rs747040126	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5701921	TGGAACAGGAGGTTC[A/G]TGACTGGTCTCCTGA	54476
rs747044009	snp	A/G	1.64784e-05	0.00287035	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5729549	GATGAAGCAGCGCTG[A/G]TCAAGAGGGGTCAAT	54476
rs747054051	snp	C/T	3.29468e-05	0.00405861	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741289	TGGTTTGTTATTTCA[C/T]GGGGCTGTTGGTTCA	54476
rs747069310	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5773733	GCCACCATGCTGGTT[A/G]ATTTTTGTATTTTTA	54476
rs747070009	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5764993	GAGGATTGCTTGAGC[A/C]CATGAGTTCCAAGTT	54476
rs747096553	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668740	GTCCCGAGGAAGAAC[A/G]CTGTTAGGAAGTAGC	54476
rs747111271	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5692180	GGAAGAGGGAACTAT[A/G]AATCGAGGCTGGCAG	54476
rs747136513	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5640669	TGATTTACGTTAATA[C/G]AATTGTTAATATTAA	54476
rs747137425	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5774840	CTCAGTTCACTGCAA[C/T]ATCCCCTCCAGAGTT	54476
rs747145243	snp	C/G			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622335	CTGCAGTGGCGCACG[C/G]GTTTTGGATGGGGGG	54476
rs747182290	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677369	TTATCTCCATTGTAA[C/G]ACTGGACTACTAATC	54476
rs747185634	snp	C/T	1.64741e-05	0.00286998	missense	RNF216	GRCh38.p7	7:5729457	ATTGCATAGTGTCCT[C/T]TGAGCTCGTGCAGGG	54476
rs747185671	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5701411	AGTTCCCCCTTTCTA[A/G]GATCTCCGTTCATCT	54476
rs747205368	snp	C/T	3.30753e-05	0.00406652	missense	RNF216	GRCh38.p7	7:5623074	GCATAGGGTGGCATC[C/T]GTGGCTGTGGCAGGT	54476
rs747206782	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5764673	AAAGACTCTTCATAA[A/G]AAGCAATTAACACTA	54476
rs747220764	snp	A/C	1.79162e-05	0.00299295	missense, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711837	AAGCTACAGGACGGG[A/C]ACCTAGAGTCAGAAC	54476
rs747232763	snp	A/C	3.29468e-05	0.00405861	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741170	AGGGGCCTGAAATCC[A/C]ACCTTGCTGGGGTTC	54476
rs747241969	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5740336	TTTCACCGTGTTAGC[A/C]AGGATGGTCTTGATA	54476
rs747273538	snp	A/C/T	1.648e-05	0.0028705	missense	RNF216	GRCh38.p7	7:5721127	GACCTACAATGTCGT[A/C/T]GCTTATTTTCAAGAA	54476
rs747276324	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667547	CAGGAGCAGGGCCAT[A/G]CATAGGAAGCAGATC	54476
rs747312376	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5758603	TGTGGAGTCAAAGGA[A/G]GTTATTTTGGACCTT	54476
rs747319191	in-del	-/TTCT			intron-variant	RNF216	GRCh38.p7	7:5749890	ATGGGTTTTTATGGC[-/TTCT]TTATTTGAAACACTG	54476
rs747325511	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5720404	CTAGCTTACCTTATT[C/T]TAAGAATACAGCATG	54476
rs747343036	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5686858	CTCAGATCCCTTGCA[C/T]GAGCAGTTCACAACA	54476
rs747348422	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5697854	GCCTTGAAGCTAAGA[A/G]GGCTGTGGGAACACG	54476
rs747348459	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5748948	CGTGTCTATATATGC[A/G]TTATGTGTGTGTGGT	54476
rs747360336	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5650842	ACATGGGCCTCAGCC[A/G]CCTCATCTGTAAGAG	54476
rs747386567	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676725	AATAATGGCATTTCC[A/G]GCCTAACAACTGGGA	54476
rs747391214	in-del	-/ATGTGTCT	1.66601e-05	0.00288614	intron-variant	RNF216	GRCh38.p7	7:5641140	AAGCAATAGGCAGCC[-/ATGTGTCT]ACTTACAGTGGGATC	54476
rs747415238	snp	A/C/T	3.45197e-05	0.00415435	intron-variant	RNF216	GRCh38.p7	7:5721223	AACTATGTGTTAGGA[A/C/T]CCTGGGCCAGCCATG	54476
rs747419024	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5659093	CACTAGCGAGATTGG[C/T]GGAAACATGAACTTA	54476
rs747430560	in-del	-/TTTTTTGA			intron-variant	RNF216	GRCh38.p7	7:5715754	TTTTTTTTTTTTTTT[-/TTTTTTGA]GATGGAGTCTCACTC	54476
rs747438165	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5749506	CTAGAAATCTGATAT[A/G]TCTTGGTATAAATGC	54476
rs747462330	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5735006	AAATACAAAAACTAG[-/C]TGGGCGGTGGGCACC	54476
rs747465105	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5661345	GAACTTACAGGTGTG[C/T]GCCACCATGCCCAGC	54476
rs747491123	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5768956	ATGAGCCACTGTGCC[C/T]GGCCAAAGCAACTTT	54476
rs747497628	snp	A/C			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672066	CATTGATGACTATCA[A/C]GGAGTAGATGGCAGT	54476
rs747500697	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5770709	GAGGATTTACAGTAG[C/G]AGATATTGTATTACT	54476
rs747519344	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5719572	AATGTGAATATCACC[A/G]AGAATAAAAGACTAC	54476
rs747525981	snp	C/T	1.64751e-05	0.00287007	missense	RNF216	GRCh38.p7	7:5721044	CTACCTCTGCCATCT[C/T]TTTGATTTTCTGCTC	54476
rs747533081	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5695944	GTTTCCCGTCAGAAC[A/G]CATCCAAGGAACAGA	54476
rs747555044	snp	C/G			intron-variant, downstream-variant-500B	RNF216, RNF216-IT1	GRCh38.p7	7:5662214	TTTCTTACTGGTAAC[C/G]ATAGGAACCTGCTAA	54476
rs747559626	snp	A/G	3.29478e-05	0.00405867	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741321	AGACTGGAAGTAAGG[A/G]TGATCTAACCAGCAG	54476
rs747567101	snp	C/G	1.6513e-05	0.00287336	missense	RNF216	GRCh38.p7	7:5641159	GTCTACTTACAGTGG[C/G]ATCGGTCCAGAGAGA	54476
rs747579721	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676741	GCCTAACAACTGGGA[C/G]AGAAAGAAAACTCCT	54476
rs747582557	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5743932	CCAATTAAGATCCTC[C/T]ATAGAGAAACAACAT	54476
rs747591834	in-del	-/TTTTTTTT			intron-variant	RNF216	GRCh38.p7	7:5715737	ATCACCAACTCATTC[-/TTTTTTTT]TTTTTTTTTTTTTTT	54476
rs747598266	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5714549	AGGCGTGAGCCACCC[A/G]GGCAAAAAGTCATCT	54476
rs747598356	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5704350	GCCCTTAGTCTCACA[C/T]GGGTCAAAATTAGCT	54476
rs747609095	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5645204	TGACTCTGATGTGTC[A/G]TGGTGTGGACTTCTT	54476
rs747613195	snp	A/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670947	GCCTCTCCCTTCCCT[A/T]GGAGGCCTAGAGTGT	54476
rs747615490	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5778118	CACAAATCTCACCAT[A/G]GTGAAACCGAAATCC	54476
rs747617326	snp	C/T	1.64776e-05	0.00287028	missense	RNF216	GRCh38.p7	7:5761008	AACAACTTACCTTGT[C/T]CCCGATGGCAGTGAA	54476
rs747620185	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5657709	CATCTGTGTCTTCTA[C/G]TTGTCAAAGATGCTG	54476
rs747633732	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666383	AGGCCTCTCTGCGAA[A/G]GTGCATGTAAGTGAA	54476
rs747656620	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5634525	AGCAGAGCTTGGAGT[A/G]GCACATGCTGCGCAG	54476
rs747664990	snp	A/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753796	GGTCAGGAGTTTGAG[A/T]CCAGCCAGACGAACA	54476
rs747670544	snp	A/G	0.000200743	0.0100165	intron-variant	RNF216	GRCh38.p7	7:5760493	TGCACTCTGGCCTGG[A/G]CAATGAGTAAAATTC	54476
rs747676731	snp	C/T	1.65351e-05	0.00287528	missense, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712755	CCGCAACCTCCTCCT[C/T]GGCTTTTCGCTCATA	54476
rs747693423	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681658	AGTCCCATTCCTCAA[C/T]TGGGGATAGTTTTCT	54476
rs747708456	in-del	-/GGCAGGGGG	1.64988e-05	0.00287213	cds-indel	RNF216	GRCh38.p7	7:5623032	ACAGGCCGCACGGGA[-/GGCAGGGGG]AAGGGTGGGTGCGCG	54476
rs747721558	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5729697	AAAAGAATAACATTT[A/G]TTCTAATTACTCTAT	54476
rs747754554	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5744835	AAATTAGCTGGGAGT[C/G]GTAGCGCATGCCTGT	54476
rs747768115	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5690147	CAGCCTGGCCATGGT[A/G]AAACCCTGTCTCTAC	54476
rs747773226	snp	C/G	3.29669e-05	0.00405984	missense	RNF216	GRCh38.p7	7:5725366	AATACTGGTTCATTT[C/G]TTTTCTCTTCTTCCT	54476
rs747780115	snp	C/T			missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752945	ATCTGAGGAGTCAGA[C/T]ATGGTGATGGGCCCA	54476
rs747781708	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5648727	GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAG	54476
rs747792565	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5764639	GGCAACAGAGCAAGA[C/T]ACCGTCTCAAAAAAA	54476
rs747800746	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5656248	CACTCCAGCCTGGGC[A/G]GCAGAGCAAGATTCA	54476
rs747809161	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5778686	TGAGTTCAAGTTCCA[C/T]GCTGACCCTTACAAG	54476
rs747810521	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680806	TGAAGGACACAGCCA[C/T]CCACTGGCTGCTCAT	54476
rs747828682	snp	C/T	1.73915e-05	0.0029488	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5740984	TTACCGTTTCTTTCA[C/T]TAGTAGTTCAACGAG	54476
rs747828748	snp	C/T	3.45149e-05	0.00415406	intron-variant	RNF216	GRCh38.p7	7:5725289	AAAGGTACAGTGTTG[C/T]AGCTACACACTGCCA	54476
rs747836604	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5779933	TTTCCGAGGGACGCG[C/G]ATATGCTCTGGTCCC	54476
rs747854176	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5643864	CCTGCAACCCACAGC[A/G]TGCTTTTGGGCTCTA	54476
rs747854533	snp	A/T	1.74245e-05	0.0029516	missense	RNF216	GRCh38.p7	7:5622870	GGCCATCAGAAGCGA[A/T]GCCGCGGCTGGGGGC	54476
rs747870714	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5647971	CCATGACATTCATTT[A/G]CTTAGAAGTATTTCA	54476
rs747875851	snp	C/T	0.000149399	0.00864159	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739560	AAGGTCTTGAGAGAT[C/T]TGGTTCTCTGTCCCC	54476
rs747876633	in-del	-/AA			intron-variant	RNF216	GRCh38.p7	7:5777838	TCAAAAATTAAACTC[-/AA]AATCTTCAGTGGGCG	54476
rs747882809	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5698766	GGTCCCTACCACTTA[C/T]ATAGAAGAATCTTGT	54476
rs747916787	in-del	-/GT			intron-variant	RNF216	GRCh38.p7	7:5686491	GTTATCTGTTCTCTG[-/GT]GTTAAGTGCTGCTTA	54476
rs747923197	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5655712	GGAGTTTAACATTTG[A/G]AGCTCTCTCTGTGTA	54476
rs747924560	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5724390	AAGTCAACTATCTTG[A/C]AAAATAGCACTTTCT	54476
rs747975314	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5689101	ATATCCTATTATATG[A/G]CACCACCATCAGTGC	54476
rs748010065	snp	C/G	1.64947e-05	0.00287177	intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652365	AAAAAGCAGGTTAAT[C/G]GGGAAGTTGAGAATC	54476
rs748034674	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5649269	TGGTAGCAGGCGCCT[A/G]TAATCCCAGCTACTC	54476
rs748035268	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5630306	GCTTGAGTGCATATG[C/T]AGCTCTACCCCCACT	54476
rs748038227	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681773	CTTACTGACTGGCCA[C/T]GGCATCTCATCAACA	54476
rs748052073	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674567	CAGGAGGTCGAGGCT[A/G]CAGTGACCTATGATC	54476
rs748054248	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5735027	GGTGGGCACCTGTAA[C/T]CCAAGCTACTCAGGA	54476
rs748063362	snp	C/G	1.64792e-05	0.00287042	missense	RNF216	GRCh38.p7	7:5641306	ACATGCGGTTGCAGC[C/G]TTCAGATTTGATGAG	54476
rs748065015	snp	A/G	1.6701e-05	0.00288968	intron-variant	RNF216	GRCh38.p7	7:5715218	AAGAAACACACATGA[A/G]ATGTCCTGCACTTAA	54476
rs748065974	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5684424	CAAGCTGGGCCTTCT[A/C]AGCCGAGCCTCTGCA	54476
rs748145986	snp	A/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675016	AACAAACAAACAAAC[A/T]ATATATATATATAAA	54476
rs748166384	in-del	-/AGG			intron-variant	RNF216	GRCh38.p7	7:5765536	TCAGGAAGCTGAAGC[-/AGG]AGGACTGCTTGAGCC	54476
rs748177680	snp	C/G	3.29457e-05	0.00405854	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741161	GAGGAGAAGAGGGGC[C/G]TGAAATCCCACCTTG	54476
rs748212381	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5690051	GTTTTATGGCCAGGC[A/G]CGGTGGGTGGCTCAT	54476
rs748214112	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5718280	CAGCTACTAAGGTGG[C/G]TGAGGCAGGAGAAGC	54476
rs748228494	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5648286	TAATTTTGTATTTTT[A/G]GTAGAGACAGAGGTT	54476
rs748235479	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5623264	GGGCAGCGACCTCTG[C/G]ACACGGGAGTGGCTC	54476
rs748254168	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5684252	GGACTACAGGCACCC[A/G]CCACCACGCCCAGCT	54476
rs748266152	in-del	-/AAGGAAGGAAGGG			intron-variant	RNF216	GRCh38.p7	7:5755214	GGGAGGGAAGGAAGA[-/AAGGAAGGAAGGG]AAGGAAGGAAGGGAG	54476
rs748291749	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5692399	CGGGTGAATCAGAAC[C/T]CATCCTTGTTAGTCA	54476
rs748294894	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5708023	GGAGCCACCATGCCC[A/G]GACAGTGTGTTTAGT	54476
rs748307665	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5642546	CACTGCAACCTCCAT[G/T]TCCTGGGTTCAAACG	54476
rs748329404	snp	C/T	3.29935e-05	0.00406149	missense	RNF216	GRCh38.p7	7:5623023	TTGTTGAACACAGGC[C/T]GCACGGGAGGCAGGG	54476
rs748337849	snp	A/T	2.76339e-05	0.00371701	intron-variant, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711736	ATAATTCAATATACA[A/T]CTAGAAAAAAATGTG	54476
rs748340518	snp	C/G	1.64792e-05	0.00287042	intron-variant	RNF216	GRCh38.p7	7:5721017	CACACCCCAAGACCA[C/G]AGCACATCTTCCTAC	54476
rs748341295	in-del	-/TT	1.6477e-05	0.00287024	frameshift-variant	RNF216	GRCh38.p7	7:5761056	ACCTCTTCATTGTTG[-/TT]TCCCTCTTCCATTTT	54476
rs748347602	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5653875	CTGGCAGGCAAAGCC[A/G]GGCATGTTCAGTTCC	54476
rs748350948	snp	A/G			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622489	CCCCTCCAGGGAGAT[A/G]CTCTCGGCTGCCTTG	54476
rs748359098	in-del	-/GG			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671913	TGCAAGCCAAGGAGA[-/GG]GGGGCCTCACAAGAA	54476
rs748363302	snp	A/C/T	3.64985e-05	0.00427179	intron-variant	RNF216	GRCh38.p7	7:5741846	ATTTTAATAATTCAA[A/C/T]TTCTTTCCTATGCCT	54476
rs748369886	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5702703	ATCAAGAAGTCTGTG[A/G]TGAATAGATTCACTA	54476
rs748374866	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5742334	TTACAGGCATGAGCC[A/G]CTGAACCCAGCCCTG	54476
rs748380155	snp	C/T	1.64765e-05	0.00287019	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741082	ATTGGAAAGGCTGGA[C/T]CTGGCTCTTCATCAT	54476
rs748389354	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5652531	GATAAAGGACAGACA[C/T]AAAGACAACTCCTGG	54476
rs748391540	snp	A/G	1.66554e-05	0.00288573	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5730813	CCAGAAGAAAATTAC[A/G]AAGTCTGCAGAAACA	54476
rs748398889	snp	C/T			upstream-variant-2KB	RNF216	GRCh38.p7	7:5782560	CCCCAACTCTTAAAA[C/T]AATTGCTGGCCAGGC	54476
rs748441802	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5626010	TGCTGCTGCCTGGCC[A/T]CGTGTTCTGAGCAAG	54476
rs748444372	snp	C/T	1.64868e-05	0.00287109	missense	RNF216	GRCh38.p7	7:5716765	AGCAAAAAGTCTTCA[C/T]GCTGAAGAACAAAAA	54476
rs748463167	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678546	CCATGGCTACTTACT[A/G]AAGTGACCTCAGGTG	54476
rs748472606	snp	A/C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672460	GAATGAAACTACACA[A/C/T]ACATGATGTAGTGCT	54476
rs748483330	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5740381	TCCACCCACCTTGGC[C/T]TCCCAAAGTGCTGGG	54476
rs748489753	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5701988	ACCAGAAGGGAGCAC[C/G]AGGATGTTGTCTGGG	54476
rs748511754	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5641755	AATGGAGAGAACAGG[A/C]TGAGCATGGTGGTGC	54476
rs748549962	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667866	AGTCACTGGATCAGA[C/T]TGGGGAAAGGAGCCA	54476
rs748561164	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5651056	GAGCGGAAGTGAGAT[A/C]TATGTATATAATTCC	54476
rs748585339	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5642861	TCTACAGCACAAACC[A/T]TCTCTGTAAGAGCAC	54476
rs748593041	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5750371	AAAATTTCCAGCAAA[A/G]CAAATTTAAATATGT	54476
rs748608443	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5775729	CAAAAACTAGCCAGG[C/G]GTGGTTGCAGGCACC	54476
rs748610411	snp	C/T	1.81027e-05	0.00300849	missense	RNF216	GRCh38.p7	7:5624056	GGGAGGGGCACTTGC[C/T]TCCATTCTTTCTTTT	54476
rs748621721	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5758717	AACAGGAGTATATAC[A/G]CAATGCATGTACCCC	54476
rs748646253	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662905	AAGCGTTCCAGGTAC[A/G]GGGAATGCAAGCAGG	54476
rs748660199	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5721251	ATGTCCATTCTTCCC[A/G]GCCTCATCCTCCACC	54476
rs748670948	snp	C/T	1.92313e-05	0.00310085	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5730715	GAACATGACACTTGC[C/T]TTTGTCTCATCTTGG	54476
rs748692170	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5706363	CATGACTGAAACTTC[C/T]CACTGCACAGTGACT	54476
rs748708055	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5661605	GTCAGGAGTTTGAGA[C/T]CAGCCTGGCCAACAT	54476
rs748708523	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5730884	CCCATTGCTTCAAAT[G/T]CAATGGTTGAAGAAT	54476
rs748714004	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5710367	CCTGCCTCAAAACTT[-/A]AAAACAAAAACAAAA	54476
rs748715577	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5749701	AAAGTGCTGTGTGTT[C/T]AAAGATGTATATGCG	54476
rs748734311	snp	C/T			intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652024	TATTATTATCACAGG[C/T]GTATCATTTTGTATT	54476
rs748739124	snp	A/C			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781070	AACTTTCGCGGAACA[A/C]GCGCTCCAGATGTGA	54476
rs748742654	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5695562	GCAGAGCAGAAGACA[A/C]CGCAGCTATAGACAA	54476
rs748742656	in-del	-/GTTA			intron-variant	RNF216	GRCh38.p7	7:5706546	TGGTTTATCTGTGTT[-/GTTA]GTATGTGCCAGGAGT	54476
rs748774432	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5625416	TCTTTGCTGTGGGTT[A/G]GAATATTAATAATGA	54476
rs748785818	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5765839	TATGTGCCTGTAATC[C/T]CAGCTACTCAGGAGG	54476
rs748799448	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5716636	AAAACAAATTTGCCA[C/T]CAAAAATGCTGACAA	54476
rs748819374	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673107	ATTCCCACCACTCTC[C/T]GGACCTCCGGAGACC	54476
rs748840697	snp	C/T	1.64751e-05	0.00287007	stop-lost	RNF216	GRCh38.p7	7:5622860	GGGGATTCGGGGCCA[C/T]CAGAAGCGATGCCGC	54476
rs748847872	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5738472	CCAGCACTTTGGGAG[G/T]CCGAGGCGGGTGGAT	54476
rs748854238	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5720459	GCTCATCGACTATTA[C/T]GGGTAAGGCTTCCTG	54476
rs748856869	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5649642	AAAAACACATCACCA[C/G]ATTCCTTTGGGCATC	54476
rs748879250	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5732866	AAGTAAGCCAGGCTA[C/G]TACTCCAACCTTTCA	54476
rs748882399	snp	A/G	2.92402e-05	0.00382351	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739520	TTCCCAGATTCATCT[A/G]TCTACATAGAAGATG	54476
rs748890474	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5716162	CTCTCAAAGTGCTGG[A/G]ATTACAGGCACGAGC	54476
rs748894554	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5698054	ATACAAGCTTCTGAC[A/G]GGAAATAAAACTGAA	54476
rs748907029	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5745063	TCAAGGATATCATAC[A/G]TACACACAAACCTAC	54476
rs748924383	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5700568	AAGCTTCTGATCCCC[A/G]CAGGCTGTGACAAGC	54476
rs748958859	snp	A/C	1.65015e-05	0.00287237	missense	RNF216	GRCh38.p7	7:5721166	CTCTTTTCTATTTTT[A/C]TGTCACCTAGAAGAT	54476
rs748967371	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5705361	GGTCCAAACCAGACA[C/T]GCCTGTGAGACCTCT	54476
rs748976135	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5773235	CAAGTCCTTTTTTTT[-/C]CCCAAATAAGATTTT	54476
rs748982195	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5766942	CCTGTTCCAGAGGCT[A/G]AAAGAGAGAATAAAA	54476
rs748989052	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5769365	CTGTGATCTGCTGGC[C/G]TTGGCCTCCCGAAGT	54476
rs749007806	in-del	-/ATTTG			intron-variant	RNF216	GRCh38.p7	7:5640603	AAATCAAGAAGAAAT[-/ATTTG]ATTTGATTTCTTAAA	54476
rs749012116	snp	C/T	1.72472e-05	0.00293654	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739310	TCTTAAAATGAATTA[C/T]TTCCTCAATAAACCC	54476
rs749013323	snp	A/G			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620483	CAGGCAGGAGCCCGA[A/G]GTTCAGGCCCTGCCT	54476
rs749037144	snp	A/G	1.64727e-05	0.00286986	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741614	GAGGCCCAAGATCCA[A/G]AAATTCACCGTAGTC	54476
rs749042325	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5723932	AATGTAAATCAAGTG[A/T]AATTTCTATCTTATA	54476
rs749046665	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5701248	GTTGAAAAATCTACC[C/T]CTTTACATGGCAGAA	54476
rs749051777	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5772510	CTCCCAGGTTTAAGC[A/G]ATTCAATCCTTTCCT	54476
rs749055914	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5638896	TGCCTTGACCTCCCA[A/G]AGCTTACAGACATGA	54476
rs749061447	snp	C/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753062	CCTGACAGGGGTACA[C/G]CCTAAAGCCAACTTC	54476
rs749063680	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5707874	GCGATTACAGGCGCA[C/T]GCAACCACACCCAGC	54476
rs749063717	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5763907	AAAAATAAAACAGAC[A/G]GCAGGGCACGACAGC	54476
rs749065759	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5656439	AAAACATGAAGAACA[C/G]GGTATCGTGGCCATC	54476
rs749076914	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5774526	GCACAGTGCCTGATA[C/T]ATACTAAGTGTGACA	54476
rs749103998	snp	G/T	1.6477e-05	0.00287024	synonymous-codon	RNF216	GRCh38.p7	7:5641202	CTCCTGGCAAGGGGC[G/T]CCTGGTGAGCGGGGA	54476
rs749123091	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680985	AGAGCCTGGACTTCA[A/G]GCCATCCCACCCCTC	54476
rs749133468	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5691127	GAAGCACACCCATTT[C/G]TCTAACCGTGTGTGT	54476
rs749146208	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5714812	AATAAGATGATGAAC[A/G]AAGGAGGTGCTCCTC	54476
rs749174011	snp	C/G/T	6.59733e-05	0.00574307	synonymous-codon	RNF216	GRCh38.p7	7:5715131	AGCATCTGCGCACTG[C/G/T]GTCAGCTCCTCGAAT	54476
rs749177499	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5639374	CTGTTCATCTCTGTA[C/T]TTACACATAGAGGAG	54476
rs749188451	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668739	AGTCCCGAGGAAGAA[C/T]GCTGTTAGGAAGTAG	54476
rs749212408	snp	A/G	1.64738e-05	0.00286995	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5729540	AGCAGCTTGGATGAA[A/G]CAGCGCTGGTCAAGA	54476
rs749240431	snp	C/T	1.65181e-05	0.00287381	missense	RNF216	GRCh38.p7	7:5623060	GTGGGTGCGCGAAGG[C/T]ATAGGGTGGCATCTG	54476
rs749256887	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5763140	AACAACCCATGTCTA[C/T]TATGGAAGGAGAAAA	54476
rs749259120	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5655427	ACACGGAGAAACCCC[A/G]TCTCTACTAAAAATA	54476
rs749261016	snp	A/C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666095	GGCGTGAACCTGGGA[A/C/G]GCAGAGCTTGCAGTG	54476
rs749265726	snp	A/G	1.64751e-05	0.00287007	synonymous-codon	RNF216	GRCh38.p7	7:5729450	TCGGGTGATTGCATA[A/G]TGTCCTTTGAGCTCG	54476
rs749285667	in-del	-/AT			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678146	TACATAAATTTGCCA[-/AT]ACTCAGGCATGTGCC	54476
rs749318380	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5708725	ACAGGCCCTCTGGAG[C/G]TGCTGTAAGCTGCCC	54476
rs749337808	snp	C/G			upstream-variant-2KB	RNF216	GRCh38.p7	7:5783541	AGAAGCAAACAAAAA[C/G]AAAACAGGGAAATGA	54476
rs749345659	in-del	-/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673543	GTGGGGCAGTATGCA[-/G]GGAAGAGAGCAAGTT	54476
rs749357107	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5747692	GACGTGCATGTTGCA[A/G]TGAGTCAAGATTGCA	54476
rs749372256	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5638473	TCTTCGGATCTGTAC[A/T]CAGTAACTGCCCACT	54476
rs749376001	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5744729	TATAATCCCAGCACT[A/T]TGGGAGCCTGAGGCA	54476
rs749378284	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5650055	GCTACATGAATGCCA[A/G]AAGGTTAGAGAGAGA	54476
rs749382430	snp	A/G	1.65504e-05	0.00287662	stop-gained, intron-variant	RNF216	GRCh38.p7	7:5741767	TCAGATCTTGCCACT[A/G]GGCAGCTGGTTTGAT	54476
rs749402884	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5764122	CTTCAACCAGGGAGG[A/C]AGAGGTTGTAGAGTA	54476
rs749408415	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5755785	TCTTTGGTGTACTCA[C/T]TTTAGCTGGATACAT	54476
rs749435108	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5659421	AGAGCAAGGGTGAAG[G/T]CTTCAGGGCAGGAGA	54476
rs749442615	in-del	-/ACCACCACCACC	2.3304e-05	0.00341343	intron-variant	RNF216	GRCh38.p7	7:5739231	TATTACATATATTTT[-/ACCACCACCACC]ACCACCACAAAAAAA	54476
rs749443418	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5759039	GGGGTGGTATTTCAT[-/A]AATGATTTAGCACAA	54476
rs749448484	snp	C/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767265	AGAAGCACATCAGGA[C/G]ATGACACATTCATCC	54476
rs749452977	snp	C/G	1.64833e-05	0.00287078	intron-variant	RNF216	GRCh38.p7	7:5652522	TTTCCTGGGGATAAA[C/G]GACAGACACAAAGAC	54476
rs749474988	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5706771	CCTTTGCTGAAAGCA[C/T]CTTAGTAGTCACTTG	54476
rs749489930	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5771490	TAAAAACTCTTGCAT[A/G]TTAACTGAAAAGAAA	54476
rs749491604	snp	C/G	3.29674e-05	0.00405988	missense	RNF216	GRCh38.p7	7:5716751	TCATCTGTAGGGCAA[C/G]CAAAAAGTCTTCATG	54476
rs749501110	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5694122	TGATAGATCAAGATA[C/G]TCAGTTTTACACTAT	54476
rs749511975	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5624206	GTGAGGAGGCCGCTT[A/G]TTGCTTATGGCCATG	54476
rs749528774	snp	A/C/T	3.29457e-05	0.00405854	missense	RNF216	GRCh38.p7	7:5729478	TCGTGCAGGGCCCAC[A/C/T]TGATGTCCTGACTAC	54476
rs749544387	snp	A/C	1.67688e-05	0.00289554	intron-variant	RNF216	GRCh38.p7	7:5715228	CATGAAATGTCCTGC[A/C]CTTAAGGAGAGGGGG	54476
rs749546394	snp	A/G	1.90076e-05	0.00308277	intron-variant	RNF216	GRCh38.p7	7:5730700	GTGACTGCAAAACAT[A/G]AACATGACACTTGCC	54476
rs749551199	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5756776	ACCTGGTAAACCCAA[C/G]ACCACCATACCCAGC	54476
rs749551786	in-del	-/AAC			intron-variant	RNF216	GRCh38.p7	7:5730645	TCCCACAGAGATAAC[-/AAC]AACAACAACAACAAC	54476
rs749561759	snp	C/T	6.58968e-05	0.00573969	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741376	GCTAGAGCAGCTGAC[C/T]CTCCTAGATTTGATA	54476
rs749566593	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5649306	CTGAGGCAGTAGAGT[C/T]GCTTGAACCTGGGAG	54476
rs749581661	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5685212	GGGTGGGCATGGAGG[C/T]AGCTCCCCTGGCTGT	54476
rs749603476	in-del	-/A			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662706	AGCCCTTGTCCTCTT[-/A]AGAGTCTACTCACAA	54476
rs749616497	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5702811	TCCTGAAGCCTCCTT[A/G]CTATGACGCCAGCCC	54476
rs749695586	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5732022	GTCCCATATACTCTT[A/C]ATCTCTAAGCTCCCC	54476
rs749702415	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5704198	GCCATTCAAGTCCTC[C/T]TCCAGAGGCCGTCTT	54476
rs749704401	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5693330	ACAGAAAAAGTCTGC[C/T]GACCCCTGGTATGGA	54476
rs749712969	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5692704	AAATAAGCCTTCCAA[A/C]ACACCAGAAGAAATA	54476
rs749739000	snp	C/T	3.9976e-05	0.00447062	intron-variant	RNF216	GRCh38.p7	7:5624024	TGGCCTGGCTGCTGC[C/T]CTGTCCTGGGGGCCT	54476
rs749743097	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5760859	CATTATCTGATATAA[G/T]TCTAGTCTAACTAGT	54476
rs749817722	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5741860	ATTTCTTTCCTATGC[C/T]TATCCCTCCTTATGT	54476
rs749833511	snp	A/G	1.65113e-05	0.00287322	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712675	TAGTTTTCACAATGG[A/G]GAAGAGTTGGCAGAT	54476
rs749846641	snp	C/T	0.00292031	0.0381002	intron-variant	RNF216	GRCh38.p7	7:5760456	AGGAGGCGGAGCTCG[C/T]GGTGAGTCGAGATTA	54476
rs749853413	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5639763	CGTGCCTAGCCTTAA[-/T]TTTTTTTTTTTTTTG	54476
rs749862881	in-del	-/AAATG	0.000573499	0.016924	intron-variant	RNF216	GRCh38.p7	7:5741824	TATTTGTCTAAGAAA[-/AAATG]AAATTTTAATAATTC	54476
rs749882248	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5718816	CCTTCCAAAGCATGT[A/G]ATCATGCTGGGATTA	54476
rs749884723	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5708295	CCTTACTAATCTTCT[C/G]CCTGGTGGTGCTAAC	54476
rs749903688	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5649822	TGGCTGCTGTTTTAG[A/G]TGTCATCTCTCACCA	54476
rs749939922	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674877	TGGCACGCACCTGTA[A/G]TCCCAGCTACTCGGG	54476
rs749972397	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5708971	CCACCCAGCTTTCTC[C/T]TGTTCTCAGCAGCCC	54476
rs749981434	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5735379	ACAGAATATGATTCC[C/T]AAGAACTTAACATAT	54476
rs749995616	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5638899	CTTGACCTCCCAAAG[C/G]TTACAGACATGAGCC	54476
rs750005494	snp	C/G	1.6607e-05	0.00288153	intron-variant	RNF216	GRCh38.p7	7:5715196	GCTGGCCATCCTGCA[C/G]GCAGTCAAGAAACAC	54476
rs750034649	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5693801	TCTAAAGCTGGTCAC[A/C]CATGGCCAGGCAGCC	54476
rs750041544	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5705604	AAAAAATGAACCATA[C/T]GCCCTTTAAAAAAAA	54476
rs750058512	snp	A/G/T	3.33113e-05	0.00408102	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5729581	TAGAATAGTCAAAAA[A/G/T]GTCTATTTTAGGCAA	54476
rs750083607	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673961	TGCCTCTTGGGCTCA[A/G]GTAATTCTCCTGCCT	54476
rs750090108	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5746636	TGGAGCCAACGTCAT[A/C]CCGGTCCTGAGATAT	54476
rs750090769	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5718002	CTGGATAAGAAAGAC[A/G]GGTAAATAAAAATAC	54476
rs750107872	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5772513	CCAGGTTTAAGCGAT[A/T]CAATCCTTTCCTTCC	54476
rs750132409	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5684795	TACCTTTACAGAGTT[A/C]TTTCCTCTAGTAAAC	54476
rs750159402	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5766145	AAATTAAAAAACTAG[C/T]TGCGCGGGGTGGCAT	54476
rs750160675	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5723577	GCGTGAACCCAGGAG[A/G]CGGAGTTTGCAGTGA	54476
rs750163066	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5759878	CCTCGTGATCCACCC[A/G]CCTCGGTCTCCCAAA	54476
rs750166684	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5703026	GGCCTGAACCTGAAG[C/G]TCTTCAGAGGGACCC	54476
rs750173731	snp	A/C	1.68587e-05	0.00290329	missense	RNF216	GRCh38.p7	7:5623103	GTTCTGCGGAACGGG[A/C]CTCGGGAGGGCCTCC	54476
rs750175815	in-del	-/CA			intron-variant	RNF216	GRCh38.p7	7:5707872	CTGCGATTACAGGCG[-/CA]CGCAACCACACCCAG	54476
rs750215318	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5776263	ACTCAGAGTCCCATC[A/G]ATCAGAGAATAAAGT	54476
rs750231229	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5692862	TATACAATGTGACAC[A/G]TGCACACTCCTCCCT	54476
rs750257076	snp	A/C			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662904	GAAGCGTTCCAGGTA[A/C]AGGGAATGCAAGCAG	54476
rs750269757	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5691217	TGCCAGGTCTACCCA[C/T]GGTGAAGGGGAGACA	54476
rs750271506	snp	A/G	1.88973e-05	0.00307381	intron-variant	RNF216	GRCh38.p7	7:5641412	TTGGAGCTGGGAGGG[A/G]AGATGAGGAGGAAAA	54476
rs750290084	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5742736	GAGTAGCTGGGATTA[C/T]AGGCGCACACCTCTA	54476
rs750302887	snp	A/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671457	TTTAAAGAGGTGATT[A/T]TATTAAATGAGGCTG	54476
rs750313790	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5634085	AAATAACCATTTGAG[A/C]GCTTGGCACAAAACT	54476
rs750316080	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5652849	GAATCATTAGAAGGA[C/T]GCACAAGGAAAAATT	54476
rs750337562	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5701844	AAAGAACTGTTGAAA[A/C]AGACAACTTACTATG	54476
rs750348811	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712146	CATGATTGTATCTAC[A/G]GGCCAGAAGATTTGG	54476
rs750363974	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5751101	TAACGGCAGTCTCCT[C/T]GGTGTGCTGTGCACC	54476
rs750368750	snp	C/G	1.65343e-05	0.00287521	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752922	ACCAGCATTGGAATC[C/G]TTTCCTCATCTGAGG	54476
rs750371647	in-del	-/TTT			intron-variant	RNF216	GRCh38.p7	7:5722370	TTGCTCATTCTCATG[-/TTT]TTTTTTTTGTTTGTT	54476
rs750372582	snp	A/G	1.64738e-05	0.00286995	missense	RNF216	GRCh38.p7	7:5721101	CTGGAAGGAGAGCAC[A/G]TCGGTCATAGGACCT	54476
rs750383929	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5761407	AGAAATGGGCTAAGG[G/T]TATTAACAGGCAATT	54476
rs750392492	snp	A/G	3.3048e-05	0.00406484	synonymous-codon, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712732	GACAAGCTCGTCGGC[A/G]TAGGCTGCCGCAACC	54476
rs750407958	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5642347	GTCTCCCAAGTAGCT[A/G]GGATTACAGGCGCCC	54476
rs750408648	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768204	GCCTGTAATCCTAGC[A/G]CTTTGGGAGGCTGAA	54476
rs750414714	in-del	-/ACACAC			intron-variant	RNF216	GRCh38.p7	7:5748622	TACATACACACACAC[-/ACACAC]ACACACACACACACA	54476
rs750418086	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5632638	AAAAATTAGCCAGGC[A/G]TGGTGGTGGGTGCCT	54476
rs750422168	snp	A/G	3.40634e-05	0.00412681	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752864	TGTCAGGATGACATC[A/G]TCATCCAGGTCCTCT	54476
rs750427415	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5702334	ACATGAGGGATAAAG[C/T]AGCTGAAATACAGGG	54476
rs750430208	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5644006	GTTCACCTATGTTGT[-/A]AGCATGTATCGATAC	54476
rs750430357	in-del	-/TATTT			intron-variant	RNF216	GRCh38.p7	7:5644813	GCCTGGCTGTTTGCC[-/TATTT]TCTTTTTTTCTTTTT	54476
rs750439671	snp	C/T	1.64727e-05	0.00286986	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741421	GAGTCTTCGGATGAC[C/T]GGTTCTGAGTTTCCA	54476
rs750440865	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5689593	TTAAAGCATAAGAAA[C/T]GTAGTTTTAGGGCTG	54476
rs750469806	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5759133	TTCCCCAACCCCTCT[C/T]GTTCCTGCTCCAGCC	54476
rs750497968	in-del	-/GGGGA			intron-variant	RNF216	GRCh38.p7	7:5695047	CACTAATGGGCCAAT[-/GGGGA]GGGGACACAGATGGG	54476
rs750498034	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5711297	GAGAAACAGTCAAAT[A/G]AATAACCTACCAGAT	54476
rs750540057	in-del	-/AAAAAAAAAAAAA			intron-variant	RNF216	GRCh38.p7	7:5738088	AATAAGACTGTCTCC[-/AAAAAAAAAAAAA]AAAAAAAAAAAAAAA	54476
rs750544172	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5721577	AATTGCTAGATCATG[C/G]GATAGGCTTACTTCC	54476
rs750546821	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5687750	CTAAGGAAGGAGAAG[A/G]TAAGTGAATCCACTA	54476
rs750549178	snp	A/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5680067	CTACCCTGTTTAATG[A/T]CCATGGATAGACTTC	54476
rs750572899	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5750553	TATCTACCTGTTAGA[C/T]AGCAGGAACCTGCTT	54476
rs750574414	snp	A/C/T			intron-variant	RNF216	GRCh38.p7	7:5770592	TGTGTAGATTTAATA[A/C/T]AACCTTTATCAGGTT	54476
rs750575891	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5707036	AATCAGAGACTACCT[A/T]TTCCCCCGGTGGGTG	54476
rs750631695	snp	C/T	3.29484e-05	0.00405871	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741363	GGCCTGATCATCTGC[C/T]AGAGCAGCTGACTCT	54476
rs750632489	snp	A/C	4.98716e-05	0.00499333	synonymous-codon, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712798	GATGGTCTGGGGGAG[A/C]ACCTTCTCCAGCTCA	54476
rs750666291	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5625789	ACATTCCCTTGGTTT[C/G]GTAGATGAAAGATTC	54476
rs750666688	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5696563	CAGCCTCCTAGACAC[A/G]CGTGCCCAAGATCGT	54476
rs750668515	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678238	AGCTCCTCACCAGAC[C/T]AATAAGAAAACCAGT	54476
rs750681459	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5729046	GCACTGCTGTGTTCC[C/T]GGACTCTCTACAGAC	54476
rs750683440	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5751185	TTTCTCCAGCTGGAA[A/C]AACAACAACAAAAAA	54476
rs750685532	snp	C/T	1.64819e-05	0.00287066	synonymous-codon	RNF216	GRCh38.p7	7:5725397	TTTTCCACTGGTTTC[C/T]GGTGACAGCTCCTGC	54476
rs750687701	snp	C/T	6.61157e-05	0.00574922	missense, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712731	TGACAAGCTCGTCGG[C/T]GTAGGCTGCCGCAAC	54476
rs750737135	snp	A/G	0.000226168	0.0106317	intron-variant	RNF216	GRCh38.p7	7:5760443	ATCATTTGAACCCAG[A/G]AGGCGGAGCTCGTGG	54476
rs750743019	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5686793	ATTTTTCCACGGACA[G/T]GGCGTGGAGAGATGG	54476
rs750775455	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5744634	TTGGTTCTGAAGACT[A/C]TACAAAACAAACAAA	54476
rs750782063	in-del	-/CT			intron-variant	RNF216	GRCh38.p7	7:5630772	ACTATGCACCAGCCC[-/CT]GTCTACACACCTCAC	54476
rs750787292	in-del	-/AA			intron-variant	RNF216	GRCh38.p7	7:5761270	CCAAGGAGGTGGGTC[-/AA]AAAAAAAAAAAACCA	54476
rs750787910	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5646032	TTTAGTATGCCCAAT[A/G]TGTCCTCAGAGATGG	54476
rs750789230	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5757743	GGTAAGGACTAACTG[C/T]AAAGAGGCACAAGGG	54476
rs750809398	snp	A/C			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682215	GCCAGCCCACACTGA[A/C]TTTTTCTCAAATCTA	54476
rs750821577	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5706020	GGTCAGGAGATCAAG[A/T]TCATCCTGGCTAACA	54476
rs750837298	snp	A/G	1.6557e-05	0.00287719	missense	RNF216	GRCh38.p7	7:5622912	GGCAGGTTGTGCTCC[A/G]GGGGCATGTGGATGG	54476
rs750846990	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5687316	AGGGAGAATCACTTG[A/G]ACCTGGGAGGCGGAG	54476
rs750858333	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5636080	TCTCAAATCCAGACT[A/G]CCAGGTGCCTGTTCC	54476
rs750875172	snp	C/G	1.86371e-05	0.00305257	intron-variant	RNF216	GRCh38.p7	7:5740942	CTCAGTATATGTAGT[C/G]TCTACATTTACTTGA	54476
rs750906003	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753719	AAAAAAGCATTGGCC[A/G]GGAGCAGTGGCTCAC	54476
rs750909895	snp	C/T			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620901	CAGCCGCCCTCTGCT[C/T]CCAGAGATCCTCCCT	54476
rs750928346	snp	A/C	1.64958e-05	0.00287187	synonymous-codon, intron-variant	RNF216	GRCh38.p7	7:5741720	TTCAAATGCTGCTCT[A/C]GACTTTTTAGGCCTT	54476
rs750933450	snp	A/G	1.82463e-05	0.0030204	intron-variant	RNF216	GRCh38.p7	7:5641401	GAAAACATAATTTGG[A/G]GCTGGGAGGGAAGAT	54476
rs750939996	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5650314	GGTTTAAATAGGACC[C/T]AGTGGTGGGCTATGT	54476
rs750945148	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5649308	GAGGCAGTAGAGTCG[C/T]TTGAACCTGGGAGGC	54476
rs750956493	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5779468	GCCAGGCCATGTATT[A/G]GCCTTCTTCCTTAAA	54476
rs750984673	snp	A/C			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780733	AAAAAAAAAAAGTAA[A/C]AGAAAAAAGAACGTT	54476
rs750991998	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712640	AACACAATTTTCATC[A/G]TCTGATGCAAGTGCC	54476
rs751041475	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5703813	GAGTGTGCCTAAACC[C/T]CCACCTTGTGGCCCT	54476
rs751051162	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5773371	CCTCAACCTCCAGAA[G/T]AGCTGGGATTAAGGG	54476
rs751061451	snp	A/G	8.25294e-05	0.00642323	missense	RNF216	GRCh38.p7	7:5622940	TGGGACCGAAGTCAT[A/G]GTTGACCCGCACGTT	54476
rs751065460	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665785	AAATACAGACGACTG[C/T]TTCTCTCGAATGGCT	54476
rs751073854	snp	A/G			intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739463	AAAGACTAGAAAAGG[A/G]CTGTGAAGCAGGTCT	54476
rs751095196	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5656888	GTAGACAAATGTATC[C/T]GGCCACCACCTCCTC	54476
rs751105838	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5723689	AATTAAGTCTACAAA[C/G]TTCCCTCTAATGTAT	54476
rs751125604	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5700914	ATCTCTCCACTGCAA[C/T]TAATTTGGAGTTCTC	54476
rs751135288	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674951	GCAGTGAGCTGAGAT[C/T]GCGCCACTGCACTCC	54476
rs751140479	snp	C/G	3.4379e-05	0.00414588	intron-variant	RNF216	GRCh38.p7	7:5715003	AACATGGTCTCCTTA[C/G]ACTCCAGGAATGTGT	54476
rs751149228	snp	G/T			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620288	CCAGTTTTAAGGCAA[G/T]TAAGAGGGGGCTGTG	54476
rs751177969	snp	G/T	5.22034e-05	0.00510872	synonymous-codon, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711793	TAGGACAGCTGAACC[G/T]CTTCACATCACTGTC	54476
rs751191569	snp	C/G	1.64841e-05	0.00287085	intron-variant	RNF216	GRCh38.p7	7:5729428	GGAAGACCAAGTAGA[C/G]TACCTTTCGGGTGAT	54476
rs751197629	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5639809	CTGTCGCCCAGGCTG[C/G]AGTGCAGTGGCATGA	54476
rs751204482	snp	A/G	4.94197e-05	0.00497066	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741188	CTTGCTGGGGTTCCG[A/G]CCTTGGAAAAGCGGG	54476
rs751234065	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5709205	TGCCCTTTCCTGTGA[C/G]ACAAGACAGAAACCA	54476
rs751236270	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5774162	AATCTGGGCTTCGGA[C/T]AATACTGCCTATGTT	54476
rs751246798	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5638992	CATTTTTGAGTTGAG[A/G]TGAATAGACCATAGG	54476
rs751253895	snp	C/T	3.53888e-05	0.00420632	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752846	TTAAAGAAAACTCAC[C/T]TCTGTCAGGATGACA	54476
rs751254832	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5638382	GCAGACAGAACTTTG[C/T]GAACTTGTCCAACTG	54476
rs751257721	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5729376	CTGTTCATTCTGTTA[C/T]CATGGGAAGATGTAG	54476
rs751263351	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675962	GATCCGCCCACCTCA[A/G]CCTTCCAAAGTGCTG	54476
rs751265210	in-del	-/GAG	1.66407e-05	0.00288446	cds-indel	RNF216	GRCh38.p7	7:5752893	CTTCTTCATGCTGCT[-/GAG]GAGCTGGGGTGACCA	54476
rs751268689	snp	A/C	1.64871e-05	0.00287111	missense	RNF216	GRCh38.p7	7:5622992	GGCTGGGATAGGCCC[A/C]ATGTTGAGTGGGAAG	54476
rs751292223	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5707489	TTTTGTATCCTGCAC[C/T]TTTACTGAATATATT	54476
rs751304897	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5660385	CAAGCTCTGCCTCTT[A/G]GGTTCAAGTGATTCT	54476
rs751308444	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5718113	GGGCCAGGTGCAGTG[A/G]CTCACGCCTATAATC	54476
rs751309483	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5773140	GGGTCTCTCATTTGA[A/C]ATAATGATATTGATG	54476
rs751319798	snp	A/C/T			intron-variant	RNF216	GRCh38.p7	7:5699989	ATAAACACAAGAAAT[A/C/T]CCACCCAACAGCAGC	54476
rs751320915	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5623967	CCTCTCCTGTGCTGG[A/G]TTGAGTGCCAGGACA	54476
rs751335064	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5691710	TGGTTCTGGCCACCC[A/G]GCAGGGAGTCCATCA	54476
rs751341614	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5718899	CCTGGCCTCAAGTGA[C/T]TGCCTGCCTTGGCCT	54476
rs751349715	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5624642	GGGCCAGGCCTCGGG[A/G]AGAGGAGGAAGGTGC	54476
rs751354534	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5629725	TCAACTACTCGGGAG[A/G]CTGAGGCAGGAGAAT	54476
rs751358429	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5627684	CCTGGGAGGTGGAGG[C/T]TGCAGTGAGCCGAGA	54476
rs751366257	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5747416	CTGAGGATGATATTC[A/G]GGACCTGACAAGTAC	54476
rs751366987	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5756463	GAGCCCTAGTTATCT[C/T]GGTTCCCTGCAACCT	54476
rs751367623	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5649151	CTTTGGGAGGCTGAG[A/G]TGGGGGGATCACTTG	54476
rs751373282	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5694827	GTTCTAGGTGTTGTC[A/G]AAATAGCTAAGCATT	54476
rs751439306	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5777795	AATCCTATTATCTGT[A/G]TATTTTTACAATAGG	54476
rs751484279	snp	A/G	3.30469e-05	0.00406477	intron-variant	RNF216	GRCh38.p7	7:5716805	TTCAGACACAAATTT[A/G]GTAAAAATGACACTA	54476
rs751497957	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5743392	GCATAAACAGAAAAA[A/T]GCCTAGAGACATTGT	54476
rs751510675	snp	A/T	3.45334e-05	0.00415518	intron-variant	RNF216	GRCh38.p7	7:5741818	GAGGTTTATTTGTCT[A/T]AGAAAAAATGAAATT	54476
rs751513067	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5728630	GGGGCTTGGCCTAGA[C/T]CTTAGCATGAGCCAC	54476
rs751521302	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5634135	CGGTCCTTTTGAGAC[A/T]TTTTTTCCAACACTT	54476
rs751523698	in-del	-/TTTT			intron-variant	RNF216	GRCh38.p7	7:5774760	CCCATTCCAAGTTAC[-/TTTT]TTTTTTTTTATTGAG	54476
rs751553061	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5693908	AGCCTTAAAAATGAC[A/T]CAACGAAAATTAATA	54476
rs751562236	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5658928	TGGAGAGTGCAGCAA[C/T]GTGTCGGAGTTATGT	54476
rs751575509	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753856	AAAAATTAGCCATGC[A/G]TGGTGGCGCATGCCT	54476
rs751580349	snp	A/G	1.64784e-05	0.00287035	intron-variant	RNF216	GRCh38.p7	7:5760967	CTAAAAGAAAAAGCC[A/G]CAGGGAAAGGGATGA	54476
rs751586216	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5755033	ACCCTATCTCAGGCT[-/A]AAAAAAAAAAAGGAA	54476
rs751651090	snp	C/T	1.65108e-05	0.00287317	missense, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712725	CGAACCTGACAAGCT[C/T]GTCGGCGTAGGCTGC	54476
rs751671958	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5731219	GTTCACATTTACAGT[-/A]AAAAAACAGTCTGCT	54476
rs751680889	snp	A/T			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712996	TTCATCTCTGAGAAA[A/T]CACACTTAAATCATG	54476
rs751697546	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5751429	CTCAAAACGGAAGCA[C/T]CCATGTAAGTTTCAT	54476
rs751698451	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679079	GATACAGTGGAATGA[A/G]TAACAGCAGCAGCTA	54476
rs751700858	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5643333	AAATGGGGAAAAATC[A/G]TGGTTGATTCCTTCA	54476
rs751701167	snp	C/T	1.71199e-05	0.00292569	missense	RNF216	GRCh38.p7	7:5623120	TCGGGAGGGCCTCCA[C/T]CCTCTGCACCTTCTC	54476
rs751702196	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5698006	GATCAGCTTCTCAGA[C/T]ATAGGCAGCTTTTGA	54476
rs751732384	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663683	AGGCGGGCAGGTCAC[A/G]AGGTCAGGAGTTCGA	54476
rs751768442	snp	A/G	1.68207e-05	0.00290001	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753031	GGCACTATCACATCC[A/G]ACTCTTTAAGTTTTT	54476
rs751777063	snp	C/T	4.36557e-05	0.00467183	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5711915	CTCCATGTGGCTGTT[C/T]ATATGAAGATGGAGT	54476
rs751779177	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5687833	TCCTTTAATCTTCAG[A/T]CAACCCAGTGGGTGA	54476
rs751792052	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5688627	TTACATTTATACAAA[A/G]TGAGCAGAAGGCTCA	54476
rs751799115	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5653042	TCTCGTTAATCTCTG[C/T]AAAATCCCTGTGCCC	54476
rs751835266	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5711179	CTGAAAGATTTTAAG[A/G]CATTCTTAGTTCACA	54476
rs751847063	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5720010	TGCTTTATCAAAGAC[A/T]TTTTCAGGTGAAACT	54476
rs751853855	snp	A/T	0.000172577	0.00928757	intron-variant	RNF216	GRCh38.p7	7:5739658	AAACACAAATAAGTT[A/T]CAATCTCATGCCAGC	54476
rs751856564	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5707235	AAGACTGTCTAGGAT[A/G]TTTGGGATCCTTTGT	54476
rs751872006	in-del	-/GGA			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620708	GAGAAACATCACTCT[-/GGA]GGGCTCCCCCTCCCC	54476
rs751888616	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670901	ACCCTGGGAAGGCAG[C/G]ACTCAAGGTCTTCCC	54476
rs751894147	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678290	CTGCCATCTACAAGA[C/T]TTTCAATTATGTTCT	54476
rs751903697	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5746566	TGAGGGAGGCCTCAG[C/G]TGTCTTGACTGAGTC	54476
rs751907429	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662872	CTTCTGCTTGAGCCT[A/G]AAGGCTATCTGGTAG	54476
rs751921699	in-del	-/A	0.5	0	frameshift-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5729576	CAATTTAGAATAGTC[-/A]AAAAAGTCTATTTTA	54476
rs751938766	snp	C/G	1.81056e-05	0.00300873	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622848	GTGCTGCTCAATGGG[C/G]ATTCGGGGCCATCAG	54476
rs751949788	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5657680	AGGGACCACAGGACC[A/G]TGGGCTTCCAGGCCA	54476
rs751970717	snp	C/T	1.74955e-05	0.00295761	intron-variant	RNF216	GRCh38.p7	7:5641383	TTTTCTTCACTGAAA[C/T]AAGAAAACATAATTT	54476
rs751972356	snp	A/C	3.29495e-05	0.00405877	missense	RNF216	GRCh38.p7	7:5641276	GGTAGCACATCTGGG[A/C]ACCACAGCGGCAAGA	54476
rs751979555	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5696883	TTCCCTTGATATTCT[A/G]TATCTGATCTCTCCC	54476
rs752003293	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5702065	ACATCTGAGGCCCCA[C/G]GTCGCTGCCGGGTTC	54476
rs752013164	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5733838	ACATCATAACTCAGT[A/G]TTGTCGAAGAGTTGT	54476
rs752036668	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5706090	CCGGGCATGGTGGCA[C/T]GTGCCTGTAGTCCCA	54476
rs752038628	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5716931	TTTAAGTGGATCAGA[C/G]AGCTAGAAAATACAG	54476
rs752041957	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672869	ACAGGCAGCACACTC[C/T]CAGGATAATGCTGAG	54476
rs752050609	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5646150	ATTATACTGAGAAGA[A/G]TCTAGAAATCAGGTT	54476
rs752061541	snp	A/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682320	CACCCGTCCCTCTAA[A/T]AGGGCAGCCATGGAG	54476
rs752075507	snp	C/G	1.64923e-05	0.00287156	missense	RNF216	GRCh38.p7	7:5715117	TTGCAGAACAAGTGA[C/G]CATCTGCGCACTGCG	54476
rs752100519	snp	A/C	1.6473e-05	0.00286988	missense, intron-variant	RNF216	GRCh38.p7	7:5741650	CAGAATCATCCTGTG[A/C]CCCAGAATCAAACAA	54476
rs752115753	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5754992	AAGATCATGCCACTG[C/T]ACTCCAGCCTGGGTG	54476
rs752145566	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5636389	GAGAAAGAAAGTTAC[C/T]GTTCACCACTTGAGC	54476
rs752145607	in-del	-/AAGAAAGTTATTTTTGT			intron-variant	RNF216	GRCh38.p7	7:5646704	CTTAAAAAAAAAAAA[-/AAGAAAGTTATTTTTGT]AAAGACTATTCCTTG	54476
rs752151469	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5683380	GTTGGAGGCTCACTG[A/C]AGCTTCCAACTCTAT	54476
rs752157557	in-del	-/ATATTAACT			intron-variant	RNF216	GRCh38.p7	7:5756418	GCCCGCGAGGCTAAA[-/ATATTAACT]ACTTAGCTCTTCAAA	54476
rs752158280	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5640209	GACCCTCTCCCCCAG[C/T]TTTTCATGTATCCCT	54476
rs752161532	snp	C/T			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620267	GCAAATACTAGATTC[C/T]TCTCTCCAGTTTTAA	54476
rs752183460	in-del	-/CACC			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754654	TGAATAAGACCCCTG[-/CACC]CACCCGCAGGAAATT	54476
rs752193464	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5725065	AGCACACTCAAATAC[C/G]TTCTCACACATGAAT	54476
rs752224343	in-del	-/G			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620162	CTACCAGAAGGTAAA[-/G]AAAAAGTTTAATGAA	54476
rs752226626	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5727122	GGCAGCAATGAGAAG[-/C]GGGGTGGCTATGATG	54476
rs752238171	snp	C/G	3.30431e-05	0.00406454	missense	RNF216	GRCh38.p7	7:5622928	GGGGCATGTGGATGG[C/G]ACCGAAGTCATAGTT	54476
rs752242819	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5657033	CCTTCCTTGCAAAGC[C/T]ACCTGGAAGGTGTCC	54476
rs752258774	in-del	-/GTTTATCATGTTAAAGTAATAAGATTTATTTTCAGTCCTTTAT	1.65897e-05	0.00288003	intron-variant	RNF216	GRCh38.p7	7:5725445	GACAAGGCCTAAAAA[lengthTooLong]TTGAGAAAAGGAAAG	54476
rs752269827	snp	A/C	3.30595e-05	0.00406554	missense	RNF216	GRCh38.p7	7:5725433	TTTAATGGCATCAGA[A/C]AAGGCCTAAAAATTG	54476
rs752269843	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5774372	GAGCCCAGGAGTTCA[A/G]TGCTGCAAGTAAGCT	54476
rs752293352	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5631409	AATCTAAGCTGCACA[A/T]GGGGGCCCAGCACTG	54476
rs752306435	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676988	CCTTAAAAGCCAAAC[C/T]AAACCAAAACCCACC	54476
rs752322571	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669668	GAGGCCAAGGTGGGC[A/G]GATCACTTGAGGTCA	54476
rs752324109	snp	A/G	1.6937e-05	0.00291002	missense, intron-variant	RNF216	GRCh38.p7	7:5741806	GTCGTGATCTCTGAG[A/G]TTTATTTGTCTAAGA	54476
rs752324749	snp	C/T	3.30246e-05	0.0040634	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741041	GCCCCCAAATGTTTT[C/T]CAAATTGGGCTCTTG	54476
rs752338491	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5718346	AGATCCTGCCACTGC[A/C]CTCCAGCCTGGGTGA	54476
rs752345141	in-del	-/GAA			intron-variant	RNF216	GRCh38.p7	7:5755152	GAGGAAGGAAAGAAG[-/GAA]GAAGGAGAAAGGAAG	54476
rs752360168	snp	A/G	3.30126e-05	0.00406266	intron-variant	RNF216	GRCh38.p7	7:5652552	CAACTCCTGGTGAGT[A/G]GACACCACAGAAGTT	54476
rs752373555	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5710993	AGTTTTGATCCATTA[A/G]TTTAGTTTATTCTTC	54476
rs752378438	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5701081	CTGTGGACAGAGAGT[A/G]CAGACCCTGAGAGTG	54476
rs752392576	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667255	AAACTGTTTCTGTTC[C/T]ACCTATATTTATTTA	54476
rs752415231	snp	A/G	3.29468e-05	0.00405861	missense	RNF216	GRCh38.p7	7:5652486	TATGTTCTTTCCAGA[A/G]TCCCTGACACTTCCT	54476
rs752415298	snp	G/T	1.65026e-05	0.00287246	intron-variant	RNF216	GRCh38.p7	7:5716791	AAAAAAGGCACACAT[G/T]CAGACACAAATTTAG	54476
rs752465467	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5701560	AGCTCTACGAGGTAG[C/G]TGCAACCGTTCTTAT	54476
rs752467043	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5709775	TTTTTTTCTTTTAAA[C/G]ACAGAGTCTTAGTCT	54476
rs752481703	snp	C/T	3.30513e-05	0.00406504	missense, intron-variant	RNF216	GRCh38.p7	7:5741743	TAGGCCTTTCTTCTC[C/T]CAACCTTTTCAGATC	54476
rs752501092	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5748713	AACAGTATGCTATTA[A/G]TAGTTAAGTAGTTAT	54476
rs752502518	snp	A/C			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676170	ATATGCCACCAGGCC[A/C]GGCTAATTTTTTTGT	54476
rs752580483	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5728046	CACAGGCCCTTCTCA[G/T]CACATTGGCAACCAA	54476
rs752588814	snp	C/T	1.74821e-05	0.00295647	missense	RNF216	GRCh38.p7	7:5624116	CCTCAATAAGCTTCT[C/T]ATCATCTTCCTAAAA	54476
rs752589295	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5749110	TAAGTAAGACCATTT[C/G]GAAAACAGCTGTGTT	54476
rs752595985	snp	A/G	1.71699e-05	0.00292996	intron-variant	RNF216	GRCh38.p7	7:5729606	AGGCAACTGAAATGA[A/G]AGAGAAGCATAAAAT	54476
rs752609543	snp	A/C	1.64982e-05	0.00287208	intron-variant	RNF216	GRCh38.p7	7:5716711	AAGGTGAGATTTCAA[A/C]CTACCTTTTGATACT	54476
rs752611737	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5660541	GTGATCCACCCATCT[C/T]GGCCTCCCAAAGTGG	54476
rs752627210	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5729889	AACTATTTTTTTTCT[A/G]TTACAGAATACGTAA	54476
rs752633657	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5726319	TGAATAAGTACAGGT[A/T]AAATCACATGACAAT	54476
rs752641930	snp	A/G	3.6959e-05	0.00429862	intron-variant	RNF216	GRCh38.p7	7:5623222	AAAAACATTAAACCA[A/G]CCTCAATGGAATCTA	54476
rs752659479	snp	A/G	1.84896e-05	0.00304047	intron-variant	RNF216	GRCh38.p7	7:5730682	GCACAGCATTTCCAG[A/G]CAGTGACTGCAAAAC	54476
rs752665806	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5719211	CATGGGGAAACCCAG[G/T]CTCTACAAAAAAAGT	54476
rs752685840	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5777869	GGGCTAAACAATTTA[A/G]CATAAAACATCAAGA	54476
rs752692482	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5624774	AGCCTCAGACACGAA[A/C]CGAAGAGGCACTGTG	54476
rs752699727	snp	A/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767092	TACAGAGACTTTGGC[A/T]CTGGCCATGACAAAG	54476
rs752710962	snp	C/G	8.23716e-05	0.00641709	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741353	CTTCTTCGATGGCCT[C/G]ATCATCTGCTAGAGC	54476
rs752727407	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5743646	TAAAAGTATGTATAT[A/G]TACCCACATGTATAT	54476
rs752744901	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5693936	ATAACTGTTCTATAA[A/G]ATGGAATTCACTTGC	54476
rs752745336	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5685722	CATGGCAAGTCACCA[C/G]CACTGCAGATGCCCA	54476
rs752747986	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5634238	TTTTCTTCTTCATTG[A/C]ACTTTTCCTCCCCTT	54476
rs752758722	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5714151	TATTTTTAGCAGAGA[C/T]GGGGTTTCACCATGT	54476
rs752785925	snp	A/G			missense	RNF216	GRCh38.p7	7:5624110	GGATTTCCTCAATAA[A/G]CTTCTCATCATCTTC	54476
rs752796747	snp	C/G			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713412	GAGGAGAGCAGAGCT[C/G]AGGGGTGGCCTGAAG	54476
rs752803327	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5769717	AGACAGTGAGAGCTG[-/T]CTCAAAAAAAAGAAA	54476
rs752815293	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5729400	GATGTAGTCAAGAGG[A/T]GTGACCCCAACAGGA	54476
rs752850733	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5704748	GGTGGGGACTTCTCT[C/T]ATTCCTCTGGTGGTC	54476
rs752870041	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5744299	TGAAGAGAGAAATTA[G/T]TGCATTGAAAGCCAG	54476
rs752902269	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680532	TCAGCCTCCTGAGTA[A/G]CTGGGACTACAGGCG	54476
rs752929444	snp	C/T	8.23662e-05	0.00641688	missense	RNF216	GRCh38.p7	7:5721109	AGAGCACGTCGGTCA[C/T]AGGACCTACAATGTC	54476
rs752950717	snp	A/C/G			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620168	GAAGGTAAAGAAAAA[A/C/G]TTTAATGAACTAATC	54476
rs752956468	in-del	-/G			intron-variant	RNF216	GRCh38.p7	7:5646835	ATCCTGATCTTTGCA[-/G]TTGGAGTACTCTGAG	54476
rs752971996	in-del	-/TTTTTTTTTTTTTTTTTTTTTTTTT			intron-variant	RNF216	GRCh38.p7	7:5660273	TTTAAATTCTTTTTT[-/TTTTTTTTTTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTG	54476
rs752972208	snp	A/G	1.64735e-05	0.00286993	missense	RNF216	GRCh38.p7	7:5641248	TCATATCCATTAATA[A/G]AAACTCGACAGAGGT	54476
rs753010499	in-del	-/CC			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681241	TGCCTAATGTAGGAA[-/CC]CCTCCCTACCTCAGG	54476
rs753018253	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5779020	AAGTGCTGGGATTAC[A/G]GGCGTGAGCCACACC	54476
rs753036691	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5658655	GAGAGAGACTGTCTC[-/A]AAAAAAAAAAAAAAA	54476
rs753039623	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5649527	GCGAGAAAAAAAACG[-/T]TTTGACATCTGGCAG	54476
rs753042729	snp	C/T	1.64727e-05	0.00286986	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741542	GGTTATGACTCGGTC[C/T]AGGCTTGGGTTCTCT	54476
rs753056209	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5735233	AACTGACACTGCCCT[C/T]GGGGACTTGAAAGAA	54476
rs753065769	snp	C/G	1.66128e-05	0.00288204	intron-variant	RNF216	GRCh38.p7	7:5641142	GCAATAGGCAGCCAT[C/G]TGTCTACTTACAGTG	54476
rs753087602	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5772297	ACAGTAGTAGTAACA[A/G]CAGAATAGTCTTTGA	54476
rs753102420	snp	C/T	2.16499e-05	0.00329006	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712906	AAAAAATCAATACCA[C/T]TTATAGAAAAATAAA	54476
rs753103362	snp	A/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664639	GCCTGTGTCCCAGCC[A/T]GGCTCTCCCCAACAC	54476
rs753149301	snp	C/T			downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619592	CGAGGGTAGCAGGGC[C/T]CTGGCACTGCAGTGT	54476
rs753149432	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5637876	TTTAAGATCAAGTCT[C/T]GTTCTGTTGTCCTGG	54476
rs753166501	snp	A/G	1.651e-05	0.0028731	synonymous-codon	RNF216	GRCh38.p7	7:5715089	CTCTTGGGCATATCT[A/G]ATGAGACACTCTTTG	54476
rs753168314	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5751310	GTTTGGTCAGGTCCT[A/G]GGTGAAAGCCTAACA	54476
rs753194698	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5716371	AAAATTAGCTGGGCA[-/T]TTTTTTTTACATACA	54476
rs753196591	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664021	GACCTGGAGGGGCTC[C/G]TAATCAACCACCGTA	54476
rs753205837	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5747199	AATTCCTGACTTACA[A/T]GCTACGGATAAAAAC	54476
rs753207256	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5732764	CAGTGGGGAAGCCTG[G/T]CGGACTTCAATCTGC	54476
rs753214122	snp	A/C/T	4.95506e-05	0.00497727	intron-variant	RNF216	GRCh38.p7	7:5729405	AGTCAAGAGGTGTGA[A/C/T]CCCAACAGGAAGACC	54476
rs753214328	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673708	CAGCATGACCTTGTC[C/T]CTACAAAAAAATTAA	54476
rs753216073	snp	C/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753919	AGAATCGTTTGAACT[C/T]GGGAGGCAGAGGTTG	54476
rs753281424	snp	C/T	3.33539e-05	0.00408361	missense, intron-variant	RNF216	GRCh38.p7	7:5741793	TTGATGAGATTGGGT[C/T]GTGATCTCTGAGGTT	54476
rs753300348	snp	C/G	1.64819e-05	0.00287066	utr-variant-5-prime	RNF216	GRCh38.p7	7:5761081	CCATTTTCAAATGCA[C/G]ACATGCATATATGGG	54476
rs753308374	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674811	GACCAGCCTGACCAA[C/T]ATGGCAAAACCCCAT	54476
rs753309447	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5705212	GAGCACCTACTATGT[C/G]CCAGGCATTGTAAAA	54476
rs753316677	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5658750	CCTTTTAAATTTTCT[A/G]TATCTGTGTATGTTT	54476
rs753317229	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669792	AGCTACTCGGGAGGC[C/T]GAGGTAGGAGAATTG	54476
rs753319340	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5759607	TAGGCTATTCGTACT[G/T]AAGTTTTGGTGGAGT	54476
rs753323285	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5717822	GAGTCTCACTTTGTC[A/G]CCCAGGCTGGAGTGC	54476
rs753346261	snp	A/C			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622823	CACACTCCTACCCCA[A/C]ACGGGCTTTGTGCTG	54476
rs753378167	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5748711	CAACAGTATGCTATT[-/A]AGTAGTTAAGTAGTT	54476
rs753396617	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5746630	ACATCTTGGAGCCAA[A/C]GTCATCCCGGTCCTG	54476
rs753412104	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5683618	GTTGCAATCCTGGCT[C/T]TACCCCTTTGAGTGC	54476
rs753434053	snp	A/G	1.6473e-05	0.00286988	missense	RNF216	GRCh38.p7	7:5652465	GCTCTTCACAGGTGA[A/G]GCCATTATGTTCTTT	54476
rs753442382	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5637266	GTGGGCTGCACCTCC[C/T]GATCACCCAGCAAAA	54476
rs753443942	snp	C/T			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622227	GATGAGAAAGTTAGG[C/T]GGCAACAGAACAAAA	54476
rs753499667	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5702089	CGGGTTCTCGGAGCC[C/T]ACGCTGACTCTAGAC	54476
rs753504916	snp	C/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754469	CATGCCTGACTTAAT[C/T]GTGGATTTTTAAGGA	54476
rs753513185	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5657727	GTCAAAGATGCTGGT[C/T]CTCCCCACCCATACG	54476
rs753533709	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5750368	ATCAAAATTTCCAGC[A/C]AAGCAAATTTAAATA	54476
rs753538833	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5726790	GTGAACCTGGAAAGC[A/G]GAGGTTGCAGTGAGC	54476
rs753597899	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5701653	TGAGTGGAGGAGCTA[G/T]AATTAAAGCATAAGT	54476
rs753645952	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5764668	AAAAAAAAGACTCTT[A/C]ATAAGAAGCAATTAA	54476
rs753645994	in-del	-/AA			intron-variant	RNF216	GRCh38.p7	7:5654688	CCAGACTCCGCCTCA[-/AA]AAAAAAAAAAAAAAA	54476
rs753662477	snp	A/G			missense	RNF216	GRCh38.p7	7:5641264	AAACTCGACAGAGGT[A/G]GCACATCTGGGCACC	54476
rs753665259	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5773696	CCTCAGCCTCCCTGA[A/G]TAGCTGGGACGACAC	54476
rs753707871	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677847	GAATCAGGGGAAGGA[A/G]GATACTGGAATGTAA	54476
rs753717097	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5710889	GCTGCAAGATGCCAG[A/C]GACTGTTGTGACAAT	54476
rs753734060	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5740678	AAGGGTTTCCATTTG[C/G]AGTGAACTCAAGGAA	54476
rs753738864	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5776099	AATCAATACAGAAAA[A/G]GTTTACTGTTAGCTC	54476
rs753739330	snp	A/G	5.07061e-05	0.00503492	missense	RNF216	GRCh38.p7	7:5623107	TGCGGAACGGGCCTC[A/G]GGAGGGCCTCCACCC	54476
rs753739633	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5775416	ATTTTTCCTTATGTA[C/T]ATGCTCCTAAACTAC	54476
rs753752528	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5632480	GATCAGCGACCAAGG[C/T]GTCCCTGGATCAGCA	54476
rs753760347	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5687602	TGACAAGCCTCTCTG[C/T]CTGCCCCTTGTGAAA	54476
rs753765960	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5710044	CAGGCATGAGCCACT[A/G]GGCAACCAATGCAGC	54476
rs753766604	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5774231	GATAAATTGTTCAAT[C/T]TCCTAGGCCAATTTC	54476
rs753768250	in-del	-/G	1.65367e-05	0.00287543	intron-variant	RNF216	GRCh38.p7	7:5716814	AAATTTAGTAAAAAT[-/G]ACACTAACCATTTAG	54476
rs753812307	in-del	-/GC			intron-variant	RNF216	GRCh38.p7	7:5661797	AGACAATGAGACTCT[-/GC]GCTCAAACAAAAACA	54476
rs753825781	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5749340	ATTTTTAGTAGAGAC[A/G]AGGTTTCACCATGTT	54476
rs753846183	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5651496	CTTAGCCTCCCAAAA[C/T]GCCAGGATTACAGGC	54476
rs753855311	snp	C/G	1.64732e-05	0.0028699	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741206	TTGGAAAAGCGGGCC[C/G]TGGGAATTCATGCTG	54476
rs753857164	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5640413	AATGCCCTGAAATGG[C/T]TCTCATCACACTCCA	54476
rs753863949	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5624957	ACCCGTGATGCCTGC[C/T]TCATGAGTGGCGCTT	54476
rs753865681	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5660436	AGATGGGAATACAGG[C/T]GCCCGCGACCACACC	54476
rs753867189	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5685791	TTTAAATATTCAAAG[C/T]CCCATTAATCCTCAT	54476
rs753867895	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5743504	AAAAGAGGTAGCTCA[C/G]TCTGTACTGAAATGG	54476
rs753888329	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5779222	TATTCATCAACTTTC[G/T]ATCTGCCTCACTCAC	54476
rs753902426	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5765499	ATAAGGCATGGTGGT[A/G]CATGCCCGTAGTCCC	54476
rs753961924	in-del	-/TGGA			intron-variant	RNF216	GRCh38.p7	7:5745673	GGAGGCTGAGGTGGG[-/TGGA]TGGATAACTTGAGGT	54476
rs753980343	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5695711	CCCCTAGTCATCCTC[A/G]GATGGATGGTGCACA	54476
rs753981128	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5778448	AGTACTTCCAACAAT[A/T]CTTTAATATACTTAT	54476
rs753981927	snp	A/G/T	0.000230596	0.0107355	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741538	GCTTGGTTATGACTC[A/G/T]GTCCAGGCTTGGGTT	54476
rs753982095	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5715415	GAGGTTTTCGTGTTT[C/T]TTTTCTGGTATTCTT	54476
rs753983074	snp	C/T	2.1985e-05	0.00331542	intron-variant	RNF216	GRCh38.p7	7:5739233	TTACATATATTTTAC[C/T]ACCACCACCACCACC	54476
rs754011074	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5744433	GAAGAAGCTGTTTCT[C/T]TGGTAGAGGAGGAGG	54476
rs754020622	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681348	AAAAATACAAACTTT[A/G]TTCTGAAAGAGAAAA	54476
rs754038032	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5645889	GCCACTGCGCCTGGC[A/T]GGTTTCTTAATTTCT	54476
rs754043322	in-del	-/CCA			intron-variant	RNF216	GRCh38.p7	7:5637008	CCAGACTGTTAACAC[-/CCA]CCACCCTCACGCTAA	54476
rs754046405	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5689501	TGGAGGCCATTTTCT[-/A]AAAAAAAACAAAAAA	54476
rs754084942	in-del	-/AAA			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768295	GTCGCTATTAGGGGG[-/AAA]AAAAAAAAAAAAGGC	54476
rs754092582	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5634855	AAAGCCCTCAGTGAC[A/G]TCGAAACCCTGTCTG	54476
rs754097284	snp	C/G			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713343	CTCTGAGAGAAATGA[C/G]GAAGATCTCCTGAAC	54476
rs754113883	snp	A/T	1.81836e-05	0.00301521	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712877	AACTAGAAAAAGGCG[A/T]AAAGGCAAAGAAAAA	54476
rs754115852	snp	C/G	1.85403e-05	0.00304464	intron-variant	RNF216	GRCh38.p7	7:5624148	GCAAGCAATGAGAAG[C/G]ATGAACCTGTAGCTT	54476
rs754117129	snp	A/G	1.64727e-05	0.00286986	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741436	TGGTTCTGAGTTTCC[A/G]AAGGATCGCTTTCTG	54476
rs754141198	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5755961	ATCATGCTCATTCAT[A/T]TATATACTGTCTATA	54476
rs754174779	in-del	-/AAAAAAAAAAAAAAAAAAAATTGGGGGGAAAACACACAA			intron-variant	RNF216	GRCh38.p7	7:5706219	GCGACACTCCATCTC[lengthTooLong]AAAAAAAAAAAAAAA	54476
rs754176482	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5723533	GCACCTGTAGTCCCA[C/G]CTACTCGGGAGGCTG	54476
rs754177424	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5705814	CGGGAGGCTGGGGCA[A/G]GAGAATTGCTTGAAC	54476
rs754185162	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5682845	AGTCCTACTCTAGGG[A/G]TCTATTCTAAGGAAT	54476
rs754214719	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680665	ACTCGGCCTCCCAAA[A/G]TGCTGGGATTACAGG	54476
rs754224270	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5655917	GCTGGAGTGCTGTAG[C/T]GTGATCTCGGCTTAC	54476
rs754234177	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675772	TGTAACGCAATGGTG[C/T]GATCTCAGCTCACTG	54476
rs754236064	snp	A/C	1.64906e-05	0.00287142	synonymous-codon	RNF216	GRCh38.p7	7:5622968	GTTGGGCAGAGGGGG[A/C]ACGTACGGGGCTGGG	54476
rs754262319	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5714310	GTTGCCCAGGCTGGA[A/G]TGCAATGGCACGATC	54476
rs754264666	snp	C/T	6.59272e-05	0.00574101	synonymous-codon	RNF216	GRCh38.p7	7:5725406	GGTTTCTGGTGACAG[C/T]TCCTGCCATTTTTTA	54476
rs754286695	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5743718	ATACATGCTAAACTG[A/G]TAACAACAGTTCCTC	54476
rs754291429	snp	G/T	3.29554e-05	0.00405914	missense	RNF216	GRCh38.p7	7:5761004	AACAAACAACTTACC[G/T]TGTCCCCGATGGCAG	54476
rs754296413	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5737467	TCCCTCCACTATTGT[A/C]CTGTGACCCTGCCTA	54476
rs754304992	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667686	TTTTGCTGGGAATCT[C/T]GGCCTGGCAGGAACA	54476
rs754308113	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753337	TGGGAATAAATGTCT[A/G]TTTTATTTAAATTGT	54476
rs754316281	in-del	-/TT			intron-variant	RNF216	GRCh38.p7	7:5749151	AAAATGCCCATGTAT[-/TT]TTTTTTTTTTTTTTT	54476
rs754321719	snp	A/G	1.65255e-05	0.00287445	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741034	GCTTCTTGCCCCCAA[A/G]TGTTTTCCAAATTGG	54476
rs754375036	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5707535	TTTTGTGGAAATTGC[A/G]GATTTTTCTATGTAT	54476
rs754387350	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665822	CAGAATCACCGAGAC[C/T]ATATCAGCAACGCCT	54476
rs754390760	snp	G/T	1.65759e-05	0.00287883	missense	RNF216	GRCh38.p7	7:5725329	TTTGCATTACCTTGT[G/T]CAAACTTGAAATCAA	54476
rs754391508	snp	C/G/T	4.96112e-05	0.00498032	missense	RNF216	GRCh38.p7	7:5622919	TGTGCTCCAGGGGCA[C/G/T]GTGGATGGGACCGAA	54476
rs754420455	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665535	GGAATAGAAGCTTTA[C/T]ATGTGGTTTCTGTGC	54476
rs754427225	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5774233	TAAATTGTTCAATCT[C/T]CTAGGCCAATTTCCT	54476
rs754444984	in-del	-/TT			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675715	ACTCTATTCAAATTC[-/TT]TTTTTTTTTTGAGGT	54476
rs754448862	snp	C/G	3.37633e-05	0.00410859	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752872	TGACATCATCATCCA[C/G]GTCCTCTTCTTCATG	54476
rs754453229	snp	C/G/T			intron-variant	RNF216	GRCh38.p7	7:5685467	GAAATTGTTCTGTTA[C/G/T]TTTCCAAGACACTAA	54476
rs754474047	snp	A/C			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620347	CCCTGCAGGGCAGAG[A/C]GAGGGAGCCAGCTGC	54476
rs754485925	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5700933	TTTGGAGTTCTCTAG[C/T]ATAGCGTATCGCCGT	54476
rs754494362	snp	C/T	1.7864e-05	0.00298859	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5740973	TAAAATAAAACTTAC[C/T]GTTTCTTTCACTAGT	54476
rs754499830	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680734	GATATCTAAAAGGCA[C/T]CCCAGACAAAAGATG	54476
rs754499982	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668357	GCCTCCCGAGTAGTT[A/G]GGACTATAGGCACCC	54476
rs754515569	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5773487	ACCTCGTGATTTCCC[C/G]GCCTTGGTCTCCCAA	54476
rs754546018	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5714509	GTGATCCGCCTACCT[C/T]GGCCTCCCAAAGTGC	54476
rs754548103	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5724862	AACCTCTTCAAAAGG[C/G]TTTTCAGCAGTTATT	54476
rs754553645	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5691021	CACCCCCTGCAGCAC[C/T]TTTTCTGCCTGTCGT	54476
rs754564803	snp	A/G			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620162	CTACCAGAAGGTAAA[A/G]AAAAAGTTTAATGAA	54476
rs754569253	snp	G/T	1.6473e-05	0.00286988	synonymous-codon	RNF216	GRCh38.p7	7:5652466	CTCTTCACAGGTGAG[G/T]CCATTATGTTCTTTC	54476
rs754613099	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5638997	TTGAGTTGAGGTGAA[C/T]AGACCATAGGGAGAC	54476
rs754620355	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5737952	AATTAGCCGGACAGG[A/G]TGGAGTACGCCTGTA	54476
rs754630220	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5725629	GCCAAGTGGGCAGAT[-/C]CCTTGAGGTCAGGAG	54476
rs754642905	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5762948	CCCTCTCTTCCTTTA[A/T]AAAGAAGTATCATGG	54476
rs754657972	snp	G/T	1.76702e-05	0.00297234	missense	RNF216	GRCh38.p7	7:5622863	GATTCGGGGCCATCA[G/T]AAGCGATGCCGCGGC	54476
rs754677616	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5722641	GTGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC	54476
rs754696892	snp	A/C/T	3.86729e-05	0.00439719	intron-variant	RNF216	GRCh38.p7	7:5641416	AGCTGGGAGGGAAGA[A/C/T]GAGGAGGAAAAAAAT	54476
rs754724016	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5685030	GAAGAGAGTGCCCAG[C/G]ATTCTTGCTGATGGT	54476
rs754734916	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5638196	TGTTTTCGATGTGAA[A/C]ATCTTCCTGTTTCTT	54476
rs754766200	snp	A/G	1.66551e-05	0.00288571	intron-variant	RNF216	GRCh38.p7	7:5715207	TGCAGGCAGTCAAGA[A/G]ACACACATGAAATGT	54476
rs754768781	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5743642	TTTCTAAAAGTATGT[A/C]TATGTACCCACATGT	54476
rs754784445	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5708547	TTTCACTTTCAGTAC[A/G]GTACTCAATAAATTA	54476
rs754798358	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5763540	AAGGCTGAGGCAGGA[A/G]AATAACTTGAACCCA	54476
rs754808244	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5728817	AGCGACCAAGAGGAG[G/T]AAGCCAAGGTCTCTG	54476
rs754813906	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5685648	AAGGAAGTAAAACAC[C/T]AGAAGCCAACCTGAC	54476
rs754816880	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5757292	TCATGTTACTAAGTA[C/T]ACAGGGATTAGCTTA	54476
rs754825004	snp	A/G	5.1079e-05	0.00505341	intron-variant	RNF216	GRCh38.p7	7:5729599	CTATTTTAGGCAACT[A/G]AAATGAGAGAGAAGC	54476
rs754828823	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5634149	CTTTTTTTCCAACAC[C/T]TCTGGTCCCCAGGGC	54476
rs754872404	in-del	-/AAAAAA			intron-variant	RNF216	GRCh38.p7	7:5776900	AGGGAGACTCTGTCC[-/AAAAAA]AAAAAAAAAAAAGAG	54476
rs754879871	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5693913	TAAAAATGACACAAC[A/G]AAAATTAATAACTGT	54476
rs754890297	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5718127	GGCTCACGCCTATAA[A/T]CCCAGCACTTTGGGA	54476
rs754905702	snp	A/G	1.76936e-05	0.00297431	missense	RNF216	GRCh38.p7	7:5623152	ACAGGCTTCTCCAGC[A/G]GGGGTCCAATGCGTT	54476
rs754907533	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5656981	GAAAATCTGAGCCCA[C/T]AGGCCAAAGTCACCG	54476
rs754909394	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5723757	ACCGTGTCTCACTCT[C/T]TGAGTCAAGCAATTA	54476
rs754924326	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5755502	TAGCCCCCTTGTGCT[C/T]TCTCCCAATTTCTGC	54476
rs754930218	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5649153	TTGGGAGGCTGAGGT[A/G]GGGGGATCACTTGAG	54476
rs754934362	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5659179	GTTCCAGACCAGCTT[A/T]CTTATTCACTCATTT	54476
rs754953817	snp	G/T	3.39616e-05	0.00412064	missense	RNF216	GRCh38.p7	7:5623113	ACGGGCCTCGGGAGG[G/T]CCTCCACCCTCTGCA	54476
rs754965452	in-del	-/A			upstream-variant-2KB	RNF216	GRCh38.p7	7:5782846	AGTGAGACTGTGTCT[-/A]CAAAAAAAAAAAAAT	54476
rs754965917	in-del	-/T	3.3534e-05	0.00409461	intron-variant	RNF216	GRCh38.p7	7:5725313	CTGCCACCAACACAG[-/T]TTTGCATTACCTTGT	54476
rs754967618	snp	A/G	3.30426e-05	0.0040645	intron-variant	RNF216	GRCh38.p7	7:5729383	TTCTGTTACCATGGG[A/G]AGATGTAGTCAAGAG	54476
rs755016232	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5756522	GCCTCAGCCTCCTGA[A/G]TAGCTGGGATTACAG	54476
rs755033799	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663516	CTGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC	54476
rs755041689	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5742289	TGGCCTCAAGTGATC[C/T]GCCTCCCTCAGCCTC	54476
rs755043406	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5702657	GGAAGAGGATGTGCT[G/T]GCGTGTGTAATTAAC	54476
rs755046862	snp	A/C			intron-variant, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711361	CAATCAAAGAAGCGT[A/C]GTTTGGACTTTGAAA	54476
rs755049416	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5635291	CCCCACTAACTTCAC[-/T]TTTTTTTTTTTTTTT	54476
rs755053999	snp	A/C	1.64811e-05	0.00287059	intron-variant	RNF216	GRCh38.p7	7:5721010	CCAGAAACACACCCC[A/C]AGACCAGAGCACATC	54476
rs755067487	snp	G/T			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713068	AAAGGACCTCTATTA[G/T]CCCAAATCACAATCC	54476
rs755073252	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5703748	TTCTTCAGTTACTCT[A/G]ATTAAACTCTCACCA	54476
rs755083580	snp	A/T	3.39403e-05	0.00411934	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752867	CAGGATGACATCATC[A/T]TCCAGGTCCTCTTCT	54476
rs755102547	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5633554	CACTCCAGCCTGGGC[A/G]ACAGAGGGAGACTCC	54476
rs755131281	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5693101	CGTCATTCTTTTAAA[C/T]GCTATGGTATATGCT	54476
rs755140708	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5777815	TTTACAATAGGAAAG[C/G]TTTTAAATCAAAAAT	54476
rs755145981	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5750646	CATGCCTAATGCATG[C/G]GCCACACAGAGTTCA	54476
rs755166629	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5653101	CTGGATTGAAGAATG[A/G]CCTACTTCAGTTCAC	54476
rs755178147	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5625779	ATTAGATAACACATT[A/C]CCTTGGTTTGGTAGA	54476
rs755180358	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5760429	GCTCAGACCGGAGAA[A/T]CATTTGAACCCAGGA	54476
rs755190951	in-del	-/TG			intron-variant	RNF216	GRCh38.p7	7:5764002	AGACCAGCCTGGCCA[-/TG]ACATGGGCGAAACCC	54476
rs755207653	in-del	-/TT			intron-variant	RNF216	GRCh38.p7	7:5769122	ACAGTTCCAAATGCC[-/TT]TTTTTTTTTTTTTTT	54476
rs755210221	snp	G/T	2.48376e-05	0.00352395	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5730795	TTGGATAATCTGGGT[G/T]TTCCAGAAGAAAATT	54476
rs755211230	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5688648	AGAAGGCTCACTCTG[C/T]GCACCTTACCTTGCT	54476
rs755233949	snp	A/C/G			intron-variant	RNF216	GRCh38.p7	7:5751270	CCAAAATGATGGTAA[A/C/G]TGAGAGTGGCACTGA	54476
rs755249738	snp	C/T			downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619583	TGCCAACAGCGAGGG[C/T]AGCAGGGCCCTGGCA	54476
rs755263260	snp	A/C	3.29457e-05	0.00405854	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741443	GAGTTTCCAAAGGAT[A/C]GCTTTCTGTGTAAAG	54476
rs755279840	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5689850	GAGGCTGAGGCAGGA[C/G]AATCACTTGAATCCA	54476
rs755299608	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5696978	TGTGTCCCTCCATTA[C/T]GCCAGCAACAGCTCC	54476
rs755302227	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5759306	TTACCCAGTCTTGGG[C/T]ATTTCTTTACAGCCA	54476
rs755307614	snp	A/C	1.90525e-05	0.00308641	intron-variant	RNF216	GRCh38.p7	7:5730702	GACTGCAAAACATGA[A/C]CATGACACTTGCCTT	54476
rs755309044	snp	G/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662895	TCTGGTAGAGAAGCG[G/T]TCCAGGTACAGGGAA	54476
rs755326602	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663753	AAATACAAAAATTAG[C/G]CGGGTGTGGTGGCGC	54476
rs755327327	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5749664	CACTTTCTGAAAGCT[C/G]TTTGCAAGCAATTAT	54476
rs755333407	snp	C/T	1.85858e-05	0.00304837	intron-variant	RNF216	GRCh38.p7	7:5624150	AAGCAATGAGAAGGA[C/T]GAACCTGTAGCTTCA	54476
rs755364803	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5651883	CAATCTCCTGACCTC[A/G]TGATCCGCCAGCCTC	54476
rs755380039	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5627300	GCCCCATACACAGCA[A/G]CCACACCAGTCAGGA	54476
rs755397608	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5766793	CTTAATTTCAAGTAA[A/C]AAATGTCTGTGGCAC	54476
rs755416252	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5751442	CATCCATGTAAGTTT[C/G]ATACTACCAAACCTA	54476
rs755420957	snp	C/T	1.64779e-05	0.00287031	missense	RNF216	GRCh38.p7	7:5761057	CCTCTTCATTGTTGT[C/T]TCCCTCTTCCATTTT	54476
rs755456229	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5745646	GGCTCACGCCTGTAA[A/T]CTCAGCACTTTGGGA	54476
rs755459963	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5721825	ACCTAGATTCACCAC[A/G]ATATATTATAACATG	54476
rs755477173	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5696026	ACCCCACTTGAAGGA[C/G]GGGCTGTGGCTCTCA	54476
rs755485817	snp	A/G	1.65151e-05	0.00287355	synonymous-codon, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712744	GGCGTAGGCTGCCGC[A/G]ACCTCCTCCTCGGCT	54476
rs755491673	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5707237	GACTGTCTAGGATAT[C/T]TGGGATCCTTTGTGG	54476
rs755493818	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678626	CTTATAAGGAGGCCG[A/G]CACTCGTAGTGACAA	54476
rs755502061	snp	A/G	0.00010011	0.00707425	synonymous-codon, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712816	CTTCTCCAGCTCACT[A/G]GTTGGGAACGAACAC	54476
rs755504353	snp	A/C			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672893	TGCTGAGGAGCCCTA[A/C]TGGATTCTATCGTTT	54476
rs755545978	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5716001	CTGCCTTGGCCTTCC[A/G]AAGTGCTGGGATTAC	54476
rs755551998	snp	C/T	2.24223e-05	0.00334823	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739496	GTGTGTCTTCAAATT[C/T]AACACTAGTTCCCAG	54476
rs755557568	snp	C/T	0.000330077	0.0128425	missense	RNF216	GRCh38.p7	7:5725407	GTTTCTGGTGACAGC[C/T]CCTGCCATTTTTTAA	54476
rs755562444	snp	C/G	5.52837e-05	0.00525726	intron-variant	RNF216	GRCh38.p7	7:5641405	ACATAATTTGGAGCT[C/G]GGAGGGAAGATGAGG	54476
rs755572169	snp	A/G			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622164	CCAGTGTACCGCAGC[A/G]GCCTGGCCTGGGAAA	54476
rs755588574	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5646195	TTGAGATTGTTTAGT[A/G]ACTTTTAAAAATTAT	54476
rs755621627	snp	A/C			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754450	GATGACAGGCATGAG[A/C]CACCATGCCTGACTT	54476
rs755622565	snp	A/C/G	4.94868e-05	0.00497407	missense, intron-variant	RNF216	GRCh38.p7	7:5741721	TCAAATGCTGCTCTA[A/C/G]ACTTTTTAGGCCTTT	54476
rs755624935	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672110	TCCCGCCCCTTTGTG[C/T]ACACGCTGTGCCCTC	54476
rs755637912	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5691744	CTAACTCTAGACACC[A/G]GAGAGTTACTAGTGT	54476
rs755641024	snp	G/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668607	ACAGGAGATATGAAC[G/T]GAGGATGAGGGTCAA	54476
rs755716968	snp	G/T	1.66101e-05	0.0028818	intron-variant	RNF216	GRCh38.p7	7:5715197	CTGGCCATCCTGCAG[G/T]CAGTCAAGAAACACA	54476
rs755718413	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5717014	TGACACATAAAACAC[C/T]TTGAACAGCAAAGAA	54476
rs755724467	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5723899	AGGCTAAGTGTGAGT[C/G]ATAAACATTAAACTA	54476
rs755725930	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5763805	TTGGATATCCCGGTC[A/T]CAAGCATTCCTTCTG	54476
rs755730154	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667292	GATGAAGCTTATGGT[A/G]ATTTATATTTCTTAC	54476
rs755731314	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669712	CAGCCTGGCCAACAT[A/G]GCAAAACCCCATCTA	54476
rs755757538	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5656274	ATTCAGTCACAAACA[A/G]ACAAACAAAGTGCTG	54476
rs755758941	snp	A/G	1.64765e-05	0.00287019	missense	RNF216	GRCh38.p7	7:5641291	CACCACAGCGGCAAG[A/G]CATGCGGTTGCAGCC	54476
rs755762293	snp	C/G	0.000104292	0.00722045	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739481	GTGAAGCAGGTCTGT[C/G]TGTGTCTTCAAATTC	54476
rs755767807	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5632452	CAGGCTGAGGTGAGA[A/G]GGAGTGGATGCTGAT	54476
rs755779318	in-del	-/ACATA			intron-variant	RNF216	GRCh38.p7	7:5748656	CACACACACACACAC[-/ACATA]ATATACTAACTAAAG	54476
rs755783427	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5694175	GGTCTTACTAAAAAG[A/G]GCATTTTGTAAACTT	54476
rs755797023	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5739770	CTTTGGGAGGTCGAG[A/G]CAGGCGGATCACCTG	54476
rs755804955	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5743356	AACTCTATCGAAAAA[G/T]GGCATATACAAGAAT	54476
rs755812160	snp	C/G			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5621009	CTGTCGTTCAGGCTA[C/G]TAGCAAAGTTCAGGC	54476
rs755836091	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5691077	AAAGAACTCTGTTCT[C/T]ACGGGTTGATCTGCC	54476
rs755837503	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5700112	ACACCCACGGGGACA[A/G]GGGGTGTTTTCATGC	54476
rs755838897	snp	A/G	3.29859e-05	0.00406102	synonymous-codon	RNF216	GRCh38.p7	7:5715125	CAAGTGAGCATCTGC[A/G]CACTGCGTCAGCTCC	54476
rs755840461	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5773706	CCTGAGTAGCTGGGA[C/T]GACACATGCGTGCCA	54476
rs755840464	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676200	TATTTTTAGGAGAGA[C/T]AGGGTTTTGCCATGT	54476
rs755844397	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5726730	TGGACGTGGTAGCAA[G/T]CGCCTGTAATCCCAG	54476
rs755844779	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5657169	AAACCTGTCAACTCA[C/T]TCTCTAGGGGGAGAG	54476
rs755878331	snp	C/T	1.64762e-05	0.00287016	missense	RNF216	GRCh38.p7	7:5729443	GTACCTTTCGGGTGA[C/T]TGCATAGTGTCCTTT	54476
rs755883175	snp	C/T	1.68917e-05	0.00290613	missense	RNF216	GRCh38.p7	7:5623105	TCTGCGGAACGGGCC[C/T]CGGGAGGGCCTCCAC	54476
rs755895480	snp	C/G	1.64735e-05	0.00286993	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5729533	GGAGGTCAGCAGCTT[C/G]GATGAAGCAGCGCTG	54476
rs755929805	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5747734	TGGCCTGGGCAACAG[A/G]AGACTCCATCTCAAA	54476
rs755975893	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5624781	GACACGAACCGAAGA[C/G]GCACTGTGAGTGCAG	54476
rs755980129	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5719310	AGCCCAGGAGGTAGG[C/T]TGAAGCAGTAAGCCA	54476
rs755991152	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5685765	AATCAAATTCATCTT[C/G]GGAAAAGAGCTTTAA	54476
rs755997444	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5771244	AACCCCTTCCTCATG[-/C]CCTTACACAAAAACA	54476
rs755999023	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5701175	CTGAACTTGAATAAC[A/G]TGGACTAAAGGAGAG	54476
rs756009628	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5638681	CTTGCTCTGTCACCC[A/G]GGCTACAGTGCAGTG	54476
rs756016394	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674398	TCCTGACCTCATGAT[C/G]CGCCTGCCTCAGCCT	54476
rs756021727	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5773690	CTCCTGCCTCAGCCT[-/C]CCTGAGTAGCTGGGA	54476
rs756040579	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5772384	AAAACTAGACAAGAA[A/T]GAATCTCCACAAACA	54476
rs756041054	in-del	-/A			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663904	GTCCGTCTCAAAAAA[-/A]CAAAACAAAACAAAA	54476
rs756064275	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5774400	GCTATGATAGCACCA[C/T]TGCACTCCAGCATAG	54476
rs756077213	snp	C/T	1.65274e-05	0.00287462	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752926	GCATTGGAATCCTTT[C/T]CTCATCTGAGGAGTC	54476
rs756155015	in-del	-/AAACA			intron-variant	RNF216	GRCh38.p7	7:5633575	GGGAGACTCCCTCTC[-/AAACA]AAACAAAACAAAACA	54476
rs756155335	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768295	GTCGCTATTAGGGGG[A/G]AAAAAAAAAAAAAAG	54476
rs756172246	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5634835	ACTGTGCTGCCCTGC[C/T]TGGGAAAGCCCTCAG	54476
rs756179563	snp	C/T	3.29674e-05	0.00405988	missense	RNF216	GRCh38.p7	7:5716741	TGTTCTTCATTCATC[C/T]GTAGGGCAAGCAAAA	54476
rs756181615	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5693957	ATTCACTTGCTGTTG[C/T]TGACCAAAAAAACAA	54476
rs756208574	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713417	GAGCAGAGCTGAGGG[A/G]TGGCCTGAAGTCAGA	54476
rs756215364	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5777941	ACAGATAAGTAAGTA[C/T]ATCCTCATGTGTGGA	54476
rs756223636	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5704767	CCTCTGGTGGTCACT[A/G]AGCCAGCTCCACCAG	54476
rs756224176	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5756641	GTTTTTTGTTTTTGC[A/G]ACAGGGTCGCTCTCT	54476
rs756235075	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5742400	TAACTCCACAGCAGA[C/T]ACAACAATGAAAGAA	54476
rs756282319	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669584	ATCAAATCTGCCAGA[C/T]ATCACTGTTGAAACT	54476
rs756283994	in-del	-/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673859	TCTCTCTTTCTCTCA[-/T]TTTTTTTTTTTTTTT	54476
rs756296916	in-del	-/GAGT			utr-variant-3-prime	RNF216	GRCh38.p7	7:5621762	TCTGTCAATGGGCCA[-/GAGT]GATGCCTCAGGCACC	54476
rs756304130	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5752542	TGATTCTGAAAAAAT[A/G]TGGGATAATATGGAA	54476
rs756321785	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5777789	TCTAAGAATCCTATT[A/T]TCTGTGTATTTTTAC	54476
rs756339470	snp	C/G	2.03631e-05	0.00319079	intron-variant	RNF216	GRCh38.p7	7:5624010	AGCAGAAGCCTGCAT[C/G]GCCTGGCTGCTGCTC	54476
rs756345098	snp	A/G	1.83626e-05	0.00303001	intron-variant	RNF216	GRCh38.p7	7:5624140	CCTAAAACGCAAGCA[A/G]TGAGAAGGATGAACC	54476
rs756360378	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5728894	GTGTGCTGTCCTTCA[C/T]GGAAGACGCCTGTGT	54476
rs756364408	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5634254	ACTTTTCCTCCCCTT[A/G]GAAAGCTGACTGGGA	54476
rs756367213	in-del	-/CATA			intron-variant	RNF216	GRCh38.p7	7:5748657	ACACACACACACACA[-/CATA]ATATACTAACTAAAG	54476
rs756408955	snp	A/C	4.94344e-05	0.00497139	intron-variant	RNF216	GRCh38.p7	7:5760993	GATGAAGTGAGAACA[A/C]ACAACTTACCTTGTC	54476
rs756422203	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5704023	TCATTCCTAAAAGCA[A/G]CACACTGAAAACAAA	54476
rs756423972	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673423	ACTGGCCTGGTTTGC[A/G]AGAAGAGAAGAAGGG	54476
rs756442697	snp	A/G	1.66239e-05	0.00288299	missense, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712799	ATGGTCTGGGGGAGC[A/G]CCTTCTCCAGCTCAC	54476
rs756470866	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5642560	TTTCCTGGGTTCAAA[C/T]GGTTCACATGTCTCA	54476
rs756526514	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712372	AGGCTACTCAGGAGG[C/T]TGAGGCATGAGAATT	54476
rs756531130	snp	A/C	0.000426621	0.0145989	intron-variant	RNF216	GRCh38.p7	7:5760450	GAACCCAGGAGGCGG[A/C]GCTCGTGGTGAGTCG	54476
rs756536259	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5770677	ATAACCAAAGCATTC[A/G]TGGAGAAAAACAAAA	54476
rs756538589	snp	C/G			downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619593	GAGGGTAGCAGGGCC[C/G]TGGCACTGCAGTGTC	54476
rs756562209	in-del	-/A	0.163265	0.234472	intron-variant	RNF216	GRCh38.p7	7:5760523	CCATCTCAAAAAAAG[-/A]AAAAAAAAAAACAAA	54476
rs756570962	snp	A/C			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665914	CTCACATCTGTAATC[A/C]CAGCACTTTGGGAGG	54476
rs756594575	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5682551	TAGCTGGGACTACAG[A/G]TGCCCACCACCATGC	54476
rs756599525	snp	C/T			missense, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712769	TCGGCTTTTCGCTCA[C/T]AGTACTTATACAGGA	54476
rs756608908	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5735299	CAAGAACTCAAGATA[G/T]GAGCTTAGAGTCAAA	54476
rs756617918	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5698202	TGTTTGGGCTAGAGG[A/G]ACACTCAAAAGGTCA	54476
rs756626561	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5776376	ATCACGAGGTCAGGA[C/G]ACGGAGACCATCCTG	54476
rs756638314	snp	A/G	3.59486e-05	0.00423946	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622853	GCTCAATGGGGATTC[A/G]GGGCCATCAGAAGCG	54476
rs756657530	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5685495	TAAGGGATGCACACT[A/G]AACATTACAACTTTG	54476
rs756676614	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5721909	GTTTTGTACTTGTTT[C/T]ACTGATTTGGCAATT	54476
rs756690726	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5628457	TAATACAACTTAAAA[C/G]TTTTTTTTCTTTTTT	54476
rs756700641	snp	A/C	1.64727e-05	0.00286986	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741570	TCTTTCTGTTTGGCC[A/C]CTTGGCTTAGTGAAT	54476
rs756700869	in-del	-/CTAG			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713770	ACATTTTAAAAATAA[-/CTAG]CTAAAATTTATGAGG	54476
rs756705205	snp	A/C	1.80788e-05	0.0030065	intron-variant	RNF216	GRCh38.p7	7:5740965	TTACTTGATAAAATA[A/C]AACTTACCGTTTCTT	54476
rs756707893	snp	A/C	1.6492e-05	0.00287154	missense	RNF216	GRCh38.p7	7:5715118	TGCAGAACAAGTGAG[A/C]ATCTGCGCACTGCGT	54476
rs756709809	snp	A/G	1.65097e-05	0.00287308	synonymous-codon	RNF216	GRCh38.p7	7:5641160	TCTACTTACAGTGGG[A/G]TCGGTCCAGAGAGAG	54476
rs756738813	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5760746	ACTGTCTCTTAAGAC[G/T]CAATGACTGCATATT	54476
rs756747169	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664654	TGGCTCTCCCCAACA[C/G]CCCCAGGGGCTGTGG	54476
rs756766303	snp	A/C	0.000171821	0.00926721	intron-variant	RNF216	GRCh38.p7	7:5715009	GTCTCCTTAGACTCC[A/C]GGAATGTGTCCTATA	54476
rs756798878	in-del	-/AAGGAAGGAAGGGAGGGAAGGAAGA			intron-variant	RNF216	GRCh38.p7	7:5755190	AGGAAAGGAAGAAGG[-/AAGGAAGGAAGGGAGGGAAGGAAGA]AAGGAAGGAAGGGAG	54476
rs756807142	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5634395	AGAGGCTTCCAAAGA[A/G]CTTAAGATTTAGTTT	54476
rs756830217	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669793	GCTACTCGGGAGGCC[A/G]AGGTAGGAGAATTGC	54476
rs756878685	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5646504	CGAGACTATCCTGGC[C/T]AACACGGTGAAACCC	54476
rs756884815	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5717049	ATCAACAAAAACAAA[C/G]TGAACAAATAAAAAC	54476
rs756884836	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5657746	CCCACCCATACGCCC[A/G]AATGACATACAGAAG	54476
rs756892619	snp	C/G			upstream-variant-2KB	RNF216	GRCh38.p7	7:5783176	ACTCTGTCAGCCAGG[C/G]TGGAGTGCGGTGGCA	54476
rs756904694	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5726952	GGAAGGGTGTGTGAG[C/G]TAAGGCCATTCCGCC	54476
rs756914396	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5725841	CACTCCAGCCTGGGC[-/A]AAAAAAAAAAAAAAA	54476
rs756916345	snp	A/G			upstream-variant-2KB	RNF216	GRCh38.p7	7:5782953	ACCTGGAATCCGAAC[A/G]TTTTGGGAAATGGAG	54476
rs756930173	in-del	-/T	1.66355e-05	0.002884	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753003	AAGCAGAGAACACTG[-/T]TACTGGGAGGTTGGC	54476
rs756948642	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5755371	ACTTAAAAAAAAATT[C/G]AAAGAATAACACAGC	54476
rs756953765	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5771670	CAGGCGCAGTAGCGG[G/T]CACCTAGTCCCAGCT	54476
rs756992044	snp	A/C	1.64825e-05	0.00287071	splice-donor-variant	RNF216	GRCh38.p7	7:5729431	AGACCAAGTAGAGTA[A/C]CTTTCGGGTGATTGC	54476
rs757007859	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5701746	CAGCAACAGCCACGC[A/G]TTTCACTGCCATTCA	54476
rs757014447	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5775458	CCTAGGGCTCTGTAG[C/T]GCCCCTGGCTCTCCA	54476
rs757027529	snp	G/T	1.64917e-05	0.00287151	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741055	TCCAAATTGGGCTCT[G/T]GAGATTCTTGCATTG	54476
rs757045404	snp	C/T	1.64871e-05	0.00287111	missense	RNF216	GRCh38.p7	7:5622994	CTGGGATAGGCCCCA[C/T]GTTGAGTGGGAAGTT	54476
rs757046985	snp	A/G	1.64732e-05	0.0028699	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741143	CTAGAGGATGGGCAG[A/G]CTGAGGAGAAGAGGG	54476
rs757058535	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5773708	TGAGTAGCTGGGACG[A/T]CACATGCGTGCCACC	54476
rs757062233	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5728523	AGGCTGCAGTGAGCC[A/G]AGATTAGGCCACTGC	54476
rs757077358	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5657251	TTCAGAAATTTCAGC[A/T]CTCTGTTCTGTCACC	54476
rs757084338	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5764749	AAACTTCAAATTCTA[C/T]GATCCCTTAAATTCT	54476
rs757094882	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5651552	ACAATCTCTGAATAA[A/C]GTCAGGAGATAGATA	54476
rs757104166	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5740729	GCAGGTATGACAGCA[C/G]CAGGCCACCATGATA	54476
rs757106327	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5725207	TGTCAGTCACTCCTT[C/G]GACTGGCCTGTCCAG	54476
rs757125082	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5691810	TTTCAAACATATTTT[C/T]GATGTTTTAAATAAC	54476
rs757158948	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5706643	CAGTAAGTGGTTTCC[A/G]TCTTGTGGCTACTGT	54476
rs757191400	snp	A/G	1.64942e-05	0.00287173	intron-variant	RNF216	GRCh38.p7	7:5720990	CCTAAGAGCAAACCA[A/G]AATCCCAGAAACACA	54476
rs757193995	snp	A/G	1.7361e-05	0.00294621	intron-variant	RNF216	GRCh38.p7	7:5741822	TTTATTTGTCTAAGA[A/G]AAAATGAAATTTTAA	54476
rs757203696	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5711244	AGTAATGCACCTAGA[C/T]AGCTCTGCTCCCACG	54476
rs757210504	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5640440	TCCAGATCTGAGGCC[A/G]GCCCCTGGGCCAATC	54476
rs757237302	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5738499	GGATCACGAGGTCAG[A/G]AGATCGAGACCATCC	54476
rs757268566	snp	C/G	1.6477e-05	0.00287024	missense	RNF216	GRCh38.p7	7:5652506	TGACACTTCCTACAG[C/G]TTTCCTGGGGATAAA	54476
rs757297752	snp	A/G	1.64746e-05	0.00287002	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741354	TTCTTCGATGGCCTG[A/G]TCATCTGCTAGAGCA	54476
rs757300320	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5631711	CCTTATACATATTGA[A/T]TAAAACAATCTTGGG	54476
rs757300405	snp	A/G			synonymous-codon	RNF216	GRCh38.p7	7:5641340	AGTCCCACACTTGTG[A/G]CATTTTCTAATGCGG	54476
rs757305899	in-del	-/T/TT			intron-variant	RNF216	GRCh38.p7	7:5722372	CTCATTCTCATGTTT[-/T/TT]TTTTTTTTGTTTGTT	54476
rs757308028	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5720189	AGCTTGATCAACAGA[A/G]ATGTGAACTGTGGGG	54476
rs757308376	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5630321	CAGCTCTACCCCCAC[C/T]ACCTAACCTGGAACC	54476
rs757318093	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5625718	AGTTTGCTGATTAAA[C/T]TTCAGATCAACAATG	54476
rs757331434	snp	C/G/T	3.44479e-05	0.00415006	intron-variant	RNF216	GRCh38.p7	7:5729608	GCAACTGAAATGAGA[C/G/T]AGAAGCATAAAATCA	54476
rs757356080	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5696898	ATATCTGATCTCTCC[C/T]TCCCTCCCACTCCCT	54476
rs757361864	snp	C/T	1.64727e-05	0.00286986	missense	RNF216	GRCh38.p7	7:5729509	TGAGCACTTTGAAGT[C/T]GGCCATGAGGAGGTC	54476
rs757379374	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5718163	AGGTGGGGGGATTGC[C/T]TAAGGTCAGGAGTTT	54476
rs757380129	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5634886	GGACACTGCTGGGGT[A/G]GCAAAACTGCCAGGG	54476
rs757380790	snp	A/T	4.94181e-05	0.00497057	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741286	ACCTGGTTTGTTATT[A/T]CACGGGGCTGTTGGT	54476
rs757404849	snp	C/T	1.72609e-05	0.00293771	synonymous-codon	RNF216	GRCh38.p7	7:5623130	CTCCACCCTCTGCAC[C/T]TTCTCCACAGGCTTC	54476
rs757444399	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671580	GAGGCCAAGGCGGGC[A/G]GATCAAGAGGTCAGC	54476
rs757444515	in-del	-/AAAC			intron-variant	RNF216	GRCh38.p7	7:5683127	ATAATTATATGGTAA[-/AAAC]AAACAAACAAACAAA	54476
rs757472363	snp	C/T	8.91464e-05	0.00667572	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5711917	CCATGTGGCTGTTCA[C/T]ATGAAGATGGAGTTT	54476
rs757493988	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5744489	GGAGGGGGACACATA[A/G]TGGTTAGTTCAAATA	54476
rs757505119	snp	G/T	1.80628e-05	0.00300517	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622851	CTGCTCAATGGGGAT[G/T]CGGGGCCATCAGAAG	54476
rs757543078	snp	G/T	0.000549149	0.0165612	intron-variant	RNF216	GRCh38.p7	7:5760426	GAGGCTCAGACCGGA[G/T]AATCATTTGAACCCA	54476
rs757553285	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680691	ACAGGTGTGAGCCAC[C/T]GCGCCCAGCACTCAA	54476
rs757554823	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5757511	TTAAGCCTATTTTCA[C/G]TAGGTACAGAATCGT	54476
rs757556752	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5743759	CTAGAAGAAAGGAGA[A/T]GGTGAATCTCAGGCT	54476
rs757575010	in-del	-/TTTA			intron-variant	RNF216	GRCh38.p7	7:5714002	TGAAAAAACATAAAC[-/TTTA]TTTATTTATTTTTCT	54476
rs757575059	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5644475	TTGGTCATTTGTACA[C/T]CTTTCTGGAGAAATA	54476
rs757596414	snp	C/T	3.30202e-05	0.00406313	missense, upstream-variant-2KB	RNF216	GRCh38.p7	7:5752953	AGTCAGATATGGTGA[C/T]GGGCCCATCTCGGAG	54476
rs757600198	in-del	-/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669932	TGCGTTTGGAAATCC[-/T]TTTTTTTTTTTTGAG	54476
rs757609147	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5731603	CACAGTAGTGCAGAC[-/A]AGAGTGGGTGGGGTA	54476
rs757612147	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5704251	GCCGTATTAATATAA[A/G]CGCCTCATTTCAGAG	54476
rs757622066	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5704996	GGGGCATAAAAAGAT[A/G]TGAATAAATGAAAAA	54476
rs757642925	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5755962	TCATGCTCATTCATT[A/T]ATATACTGTCTATAG	54476
rs757643630	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681403	ACATTTTATAGCTAC[A/G]CAGAAACAACTGTGG	54476
rs757662044	in-del	-/AA	1.65492e-05	0.00287651	frameshift-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5729576	CAATTTAGAATAGTC[-/AA]AAAAGTCTATTTTAG	54476
rs757709510	snp	C/T	0.000101673	0.00712923	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739478	GCTGTGAAGCAGGTC[C/T]GTGTGTGTCTTCAAA	54476
rs757713293	snp	A/T	1.648e-05	0.0028705	missense	RNF216	GRCh38.p7	7:5721130	CTACAATGTCGTCGC[A/T]TATTTTCAAGAAAGA	54476
rs757732048	in-del	-/AG			intron-variant	RNF216	GRCh38.p7	7:5755171	GGAGAAAGGAAGGAA[-/AG]AGAGGAAAGGAAGAA	54476
rs757744264	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5683703	CACCTTCCTCTCAGG[A/G]TTACTGTGAGGATTA	54476
rs757745366	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5778496	ATTTTGGTCTCCTCT[A/G]CTAAAACTTAAGTTC	54476
rs757767381	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5727796	CTCAACTTCCTCCTT[-/C]CTGTCTGCCTGCCTC	54476
rs757783277	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5723730	GACCATAAAAAGGAC[A/G]GAGGAGGGAGAACCG	54476
rs757791697	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5751028	TTTGGTTTTAGTTGG[C/G]GCCCTAGCCGAGGAG	54476
rs757793469	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674889	GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAA	54476
rs757793877	snp	A/G	1.67421e-05	0.00289323	missense, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712826	TCACTGGTTGGGAAC[A/G]AACACGTGCAGCTGC	54476
rs757797088	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5762766	AGCAACTTCAGGACA[C/G]TGACTATTTCTGGGT	54476
rs757798212	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5647164	GCAGTTTTTGCCAGG[C/T]TAATTCTTGCTCTGG	54476
rs757802792	snp	C/T	1.64743e-05	0.00287	missense	RNF216	GRCh38.p7	7:5641278	TAGCACATCTGGGCA[C/T]CACAGCGGCAAGACA	54476
rs757805668	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5698619	GGCTGGTCTTGAACT[C/G]ATAACCTCAAGCAAT	54476
rs757808274	snp	A/C			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713464	GCATAATGAACAGAG[A/C]ACTCTCCAGACCTTT	54476
rs757817570	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5654315	AATAAAAAGAATTTA[A/G]AAAGGGAGAAAAATG	54476
rs757849262	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5643732	TATACAATTCAGGGA[C/T]ATTTTGAGTATTCAC	54476
rs757851314	snp	A/G	3.29457e-05	0.00405854	missense, intron-variant	RNF216	GRCh38.p7	7:5741655	TCATCCTGTGCCCCA[A/G]AATCAAACAATGGGT	54476
rs757871382	snp	A/T			upstream-variant-2KB	RNF216	GRCh38.p7	7:5783210	TCTTGGCTCACTGCA[A/T]CCTCCACCTTCTGGG	54476
rs757884957	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5752707	CTAAATCTAAGAGTA[C/T]ACGAGGTAGAATGGA	54476
rs757906900	snp	A/G	1.65894e-05	0.00288	intron-variant	RNF216	GRCh38.p7	7:5725441	CATCAGACAAGGCCT[A/G]AAAATTGAGAAAAGG	54476
rs757907418	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5656120	CTAAAAATACAAAAA[G/T]TAGCCGGGCATGGTG	54476
rs757915996	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5703061	TGGGCTCTGAAGAAA[A/G]TGACTCACCTTGGAG	54476
rs757916531	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5634645	CACCTCCTCAGGTCA[C/G]ACAAGCCCAGCACCC	54476
rs757945784	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673053	TATCCATCTCTCCAT[C/T]GACTCAGGGTGGTGG	54476
rs757945800	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5653558	GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC	54476
rs757960841	snp	C/T	3.2969e-05	0.00405998	utr-variant-5-prime	RNF216	GRCh38.p7	7:5761089	AAATGCAGACATGCA[C/T]ATATGGGACTGCTAA	54476
rs757984285	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5769258	GAGTAGCTGGGACTA[C/T]AGGCGTGCGCCACCA	54476
rs757991054	in-del	-/AG	1.65202e-05	0.00287399	intron-variant	RNF216	GRCh38.p7	7:5729395	GGGAAGATGTAGTCA[-/AG]AGGTGTGACCCCAAC	54476
rs757991436	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5760969	AAAAGAAAAAGCCAC[A/G]GGGAAAGGGATGAAG	54476
rs757995905	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5636437	AGTTCAGGTTCCCAA[G/T]CAATCCCTAGTCATT	54476
rs758013906	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664690	CAGTTGCCGCCCAAG[A/G]GTAGGCTGCACGCTT	54476
rs758016726	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5746698	TTTCTAAAAATTGGA[C/G]TACTCTGCCTTCTGG	54476
rs758022692	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5747389	AAGCAGCAGAAGCAG[A/C]ATATTATTTTCCTGA	54476
rs758023783	snp	C/G/T			intron-variant	RNF216	GRCh38.p7	7:5649107	TGACGGCCGGGCGGG[C/G/T]GCGGTGGCTCACGCC	54476
rs758045429	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5731325	AATCTCTATGGTAAT[-/A]ATAAAGCTCTATGAG	54476
rs758078652	in-del	-/CTGTGG	1.65307e-05	0.0028749	cds-indel	RNF216	GRCh38.p7	7:5623073	GGCATAGGGTGGCAT[-/CTGTGG]CTGTGGCAGGTTCTG	54476
rs758116231	snp	C/T	1.64887e-05	0.00287125	missense	RNF216	GRCh38.p7	7:5622985	CGTACGGGGCTGGGA[C/T]AGGCCCCATGTTGAG	54476
rs758116890	snp	C/T	4.95511e-05	0.00497726	missense	RNF216	GRCh38.p7	7:5622931	GCATGTGGATGGGAC[C/T]GAAGTCATAGTTGAC	54476
rs758134518	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5708316	TGGTGCTAACAATGA[C/T]TGAAAGTGAGGTATT	54476
rs758138192	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5692895	ACCCTTGGTGAGCAT[A/C]CTCAAAAGCGATTCA	54476
rs758148648	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5705851	GGCGGAGGTTATGGT[A/G]AGCCAAGATCATACC	54476
rs758151365	snp	A/G	3.30513e-05	0.00406504	synonymous-codon, intron-variant	RNF216	GRCh38.p7	7:5741746	GCCTTTCTTCTCCCA[A/G]CCTTTTCAGATCTTG	54476
rs758158390	snp	C/T	1.72383e-05	0.00293578	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5740988	CGTTTCTTTCACTAG[C/T]AGTTCAACGAGCTCT	54476
rs758167305	snp	A/T	1.65059e-05	0.00287275	intron-variant	RNF216	GRCh38.p7	7:5652554	ACTCCTGGTGAGTGG[A/T]CACCACAGAAGTTCC	54476
rs758182400	snp	A/T	1.70901e-05	0.00292314	missense, intron-variant	RNF216	GRCh38.p7	7:5741811	GATCTCTGAGGTTTA[A/T]TTGTCTAAGAAAAAA	54476
rs758183889	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5711106	AAAAATGGCTTAGAG[C/T]GTATTTGTCTAGGTG	54476
rs758193299	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5647961	GTAACTTAGGCCATG[A/T]CATTCATTTGCTTAG	54476
rs758194748	snp	C/G/T			intron-variant	RNF216	GRCh38.p7	7:5728620	AAAGGTGGAAGGGGC[C/G/T]TGGCCTAGACCTTAG	54476
rs758213312	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5755441	ACAAAGGGCCATCTG[C/T]GTATAATCACCACCA	54476
rs758222126	snp	A/T	4.94197e-05	0.00497066	synonymous-codon	RNF216	GRCh38.p7	7:5652487	ATGTTCTTTCCAGAG[A/T]CCCTGACACTTCCTA	54476
rs758243805	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5658878	TAAAATTGTACATCT[C/G]CCGCTCTCAATACTG	54476
rs758252416	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5775786	AGGCAGGAGAAATGC[C/T]TGAACCCGGGATGCA	54476
rs758258914	snp	A/G	1.64882e-05	0.00287121	synonymous-codon	RNF216	GRCh38.p7	7:5622983	CACGTACGGGGCTGG[A/G]ATAGGCCCCATGTTG	54476
rs758262465	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5688638	CAAAGTGAGCAGAAG[A/G]CTCACTCTGCGCACC	54476
rs758264247	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5683906	ATTCTCCAGCCTGCA[C/G]AGAGAATAGGGACGG	54476
rs758295896	in-del	-/AT			intron-variant	RNF216	GRCh38.p7	7:5777947	AGTAAGTACATCCTC[-/AT]ATGTGTGGAGGGTAA	54476
rs758302192	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5776282	AGAGAATAAAGTCAC[A/T]AGTGTAATAAAGAGA	54476
rs758322454	in-del	-/AAA			intron-variant	RNF216	GRCh38.p7	7:5751828	TGGGATCTTTAAACT[-/AAA]AAAAAAAAAAAAAAA	54476
rs758327225	snp	A/C/G	5.54558e-05	0.00526548	intron-variant	RNF216	GRCh38.p7	7:5730683	CACAGCATTTCCAGG[A/C/G]AGTGACTGCAAAACA	54476
rs758330939	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5718044	TGCTTTTCCATAAAA[C/T]AAGGAAAGGTAAACC	54476
rs758354785	snp	A/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671458	TTAAAGAGGTGATTA[A/T]ATTAAATGAGGCTGA	54476
rs758363342	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5632730	TGCAGTGAGCCAAGA[A/T]CACGCGACTGCATTC	54476
rs758404993	in-del	-/CT			intron-variant	RNF216	GRCh38.p7	7:5696067	GCACGGCCTTGATCC[-/CT]GACTCCCAGGAGGCA	54476
rs758425001	in-del	-/TCTC			intron-variant	RNF216	GRCh38.p7	7:5705144	TTTTTCCAGCCTAGA[-/TCTC]TCTCTCCCTGTGTTA	54476
rs758426937	snp	C/G	3.94999e-05	0.00444392	intron-variant, nc-transcript-variant	RNF216, MIR6874	GRCh38.p7	7:5711909	TTCCAGCTCCATGTG[C/G]CTGTTCATATGAAGA	54476
rs758453997	snp	C/T			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622252	ACAAAACCCCCGCCG[C/T]GAGATGGGTCTGCTG	54476
rs758460722	snp	A/C			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712182	CCAAGATATGTAGAC[A/C]GAAGTTTGAGCTACA	54476
rs758465921	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5766148	TTAAAAAACTAGCTG[C/T]GCGGGGTGGCATGTA	54476
rs758467508	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5750575	AACCTGCTTAGTTCC[A/T]GAAGCCCTATAAGCT	54476
rs758469380	snp	A/G	1.64732e-05	0.0028699	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741218	GCCCTGGGAATTCAT[A/G]CTGAAACAACAAGCG	54476
rs758470395	snp	A/G	5.00948e-05	0.00500449	intron-variant	RNF216	GRCh38.p7	7:5715219	AGAAACACACATGAA[A/G]TGTCCTGCACTTAAG	54476
rs758486915	snp	C/G	5.04723e-05	0.00502331	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752876	ATCATCATCCAGGTC[C/G]TCTTCTTCATGCTGC	54476
rs758509469	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5625806	TAGATGAAAGATTCT[C/T]AGAATAAACTCCCTG	54476
rs758517663	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5650722	TCTTCGTCCCACACT[A/T]AGGACTTTCTGCTTT	54476
rs758530441	snp	A/T	1.65119e-05	0.00287327	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752940	TCCTCATCTGAGGAG[A/T]CAGATATGGTGATGG	54476
rs758531022	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5701870	CTATGAAAGCCCAGC[A/G]AAAGACGTGTCCCAA	54476
rs758555281	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5774435	CAGAGGGAGAACCTA[C/T]CTCCAAAAAAATTCA	54476
rs758585321	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662728	TACTCACAAACAGAT[A/G]ACTGTATACTCTGAG	54476
rs758630596	snp	A/C/T			intron-variant	RNF216	GRCh38.p7	7:5732374	AATGGTCTGTTTTTA[A/C/T]GTGTTTTCTCAAGTA	54476
rs758637412	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5696601	GGTCTCGCTTCGGCC[C/G]CTCTTCACCAAAGCC	54476
rs758646054	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5706048	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATG	54476
rs758648109	snp	C/G	1.9681e-05	0.00313689	intron-variant	RNF216	GRCh38.p7	7:5739247	CCACCACCACCACCA[C/G]CACAAAAAAAGCATG	54476
rs758680261	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5710014	CTGCCTCAGCCTCTC[A/G]AAGTGCTGGGATTAC	54476
rs758728249	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5742446	GAATAAGAAATGTTC[-/A]AAAAAACATATAAAA	54476
rs758735889	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5695933	ACAGAAAACATGTTT[A/C]CCGTCAGAACGCATC	54476
rs758778756	snp	C/G/T			intron-variant	RNF216	GRCh38.p7	7:5766558	ACAGGGAGAAGGCAG[C/G/T]TGTCTGAGATCCAGG	54476
rs758780591	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5649359	GCACTCTAACCTAGG[A/T]GACAGACGGAGACTC	54476
rs758802853	snp	C/G	3.18933e-05	0.0039932	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5730816	GAAGAAAATTACAAA[C/G]TCTGCAGAAACAAAT	54476
rs758815287	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5778614	ATGTACTTTCAGAAT[A/G]AATAGCACTCACTAA	54476
rs758838369	snp	C/T			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620956	AGGTACCGAAGACAA[C/T]CCTGTTGCTGCCGCA	54476
rs758845396	snp	A/G	1.64727e-05	0.00286986	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741550	CTCGGTCCAGGCTTG[A/G]GTTCTCTTTCTGTTT	54476
rs758851204	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5636148	TGGCCATGCAAGGAC[C/T]AGTCAGTATATTCAC	54476
rs758856139	in-del	-/AAAAAAAAAAAA			intron-variant	RNF216	GRCh38.p7	7:5738101	TCCAAAAAAAAAAAA[-/AAAAAAAAAAAA]AAAAAATTACAATTA	54476
rs758860045	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5737822	AGGCTGAGCACGGTG[C/G]CTTATGGCTGTAATC	54476
rs758888335	snp	C/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753762	AGCACTTTGGGAGGC[C/T]GAGGTGGGTGGATCA	54476
rs758913755	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5656909	CCACCTCCTCCAAGC[C/G]CAGCAAGTGTGATAA	54476
rs758918425	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5715653	ACTATTGAAGCTATA[A/G]CTAAAGCAGCAACCT	54476
rs758939060	in-del	-/TTT			intron-variant	RNF216	GRCh38.p7	7:5749150	AAAAATGCCCATGTA[-/TTT]TTTTTTTTTTTTTTT	54476
rs758943381	snp	C/T	4.96528e-05	0.00498236	intron-variant	RNF216	GRCh38.p7	7:5641151	AGCCATGTGTCTACT[C/T]ACAGTGGGATCGGTC	54476
rs758943700	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5658059	GCACGCACACACGGC[A/T]GGGGAGCATGCATGT	54476
rs758952620	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5644986	CGTGCCACCACGCCT[A/G]GCTAATTTTTGCATT	54476
rs758957518	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5705052	AGCATTTCTAAGCTA[A/C]TAATAATCTCCCTGA	54476
rs758985699	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676872	GCCCTGGGTCTATGA[C/G]CAGGTGTGCATCCAG	54476
rs759008343	snp	C/T	1.89256e-05	0.00307611	intron-variant	RNF216	GRCh38.p7	7:5752818	CAACTTGCAATAATG[C/T]CTCATTGTAAGTTTA	54476
rs759011711	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5744737	CAGCACTTTGGGAGC[C/T]TGAGGCAGATGGATC	54476
rs759033084	snp	G/T	1.64961e-05	0.00287189	intron-variant	RNF216	GRCh38.p7	7:5652546	CAAAGACAACTCCTG[G/T]TGAGTGGACACCACA	54476
rs759038607	snp	G/T	4.94173e-05	0.00497053	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741454	GGATCGCTTTCTGTG[G/T]AAAGAAGGCTACCTT	54476
rs759042396	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5634967	GAGGTCCCCACCCCT[C/G]TGCAAGGGCTACCTG	54476
rs759044362	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5646052	CTCAGAGATGGTTTC[C/T]ATCAACTACTTTTTT	54476
rs759063276	snp	A/G	5.00613e-05	0.00500281	stop-gained, intron-variant	RNF216	GRCh38.p7	7:5741794	TGATGAGATTGGGTC[A/G]TGATCTCTGAGGTTT	54476
rs759067925	snp	C/T	5.64308e-05	0.00531152	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739472	AAAAGGGCTGTGAAG[C/T]AGGTCTGTGTGTGTC	54476
rs759068450	in-del	-/TCTTTT			intron-variant	RNF216	GRCh38.p7	7:5715735	CAATCACCAACTCAT[-/TCTTTT]TTTTTTTTTTTTTTT	54476
rs759077729	snp	A/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677765	GAAATCCTAGGAATC[A/T]GAGTCTGCCCAAGGG	54476
rs759088273	in-del	-/AAAG			intron-variant	RNF216	GRCh38.p7	7:5747772	AAAAAAAAAAAAAAA[-/AAAG]AAAGGGGAAAAAAAA	54476
rs759094413	in-del	-/G			intron-variant	RNF216	GRCh38.p7	7:5684967	GCTTCAGGATGTGCA[-/G]GGGGGTATCAGATTT	54476
rs759095708	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5749975	AAGGTTATTATAGCT[C/T]ATAGCAATTTGGTAT	54476
rs759102534	in-del	-/GAT			intron-variant	RNF216	GRCh38.p7	7:5748913	TAACGAAGGCTATAA[-/GAT]CTGCTTCTCTGTGTC	54476
rs759113500	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5709681	AGAGCCCCTGGGAAG[C/T]TCCCACCAACATGCC	54476
rs759117099	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667180	AGATTATGACTAGTG[C/G]ATTTAAAGTTAGAAC	54476
rs759126974	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5641769	GCTGAGCATGGTGGT[A/G]CACGCCTGTAATCCC	54476
rs759140527	in-del	-/A			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620109	ATACAGGCTTTTTAC[-/A]CACAGTAGTTGAAAC	54476
rs759154660	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5640293	GCCTTGATGTAATGC[A/G]AGAAAAACCTTATCT	54476
rs759169300	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5701520	TGACACTTTACCCAC[A/G]CTGTTTCCATTGGTT	54476
rs759184147	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5775025	TGGTGAGATTACAGT[C/T]GTAAGTCACTGTGCC	54476
rs759201788	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5779061	ATGTTCTATTATCTT[G/T]AACAATAATGCAAAT	54476
rs759207236	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5757995	GAGACCCTCTCTTGA[C/T]TAAAGAAAAAAAAAT	54476
rs759212195	snp	G/T	3.29457e-05	0.00405854	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741411	CTCTGTCTCTGAGTC[G/T]TCGGATGACTGGTTC	54476
rs759219235	snp	C/T			intron-variant, nc-transcript-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662478	ATTAAGATTTGGTAA[C/T]GGCATTGCTTGAGAT	54476
rs759240483	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5720547	TTCAGCTGCACAGGG[C/G]GAAGCACTCCTAACT	54476
rs759243070	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5635653	CTGCGCTGGCCTGAG[A/G]GGAGAAGGCAGGCCT	54476
rs759252464	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5709260	GTCTGAATATTAGAT[A/T]TATGTTCCAGTCTTC	54476
rs759255012	snp	A/G	6.59076e-05	0.00574016	missense	RNF216	GRCh38.p7	7:5761015	TACCTTGTCCCCGAT[A/G]GCAGTGAAAGTTGTT	54476
rs759265957	snp	C/T	1.73018e-05	0.00294119	missense	RNF216	GRCh38.p7	7:5624104	CCTTCTGGATTTCCT[C/T]AATAAGCTTCTCATC	54476
rs759268865	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5749079	CTTTTAGTTCACGTG[A/C]CTTAGGTATTTTTGG	54476
rs759277255	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5651204	ATCACCTTCAGGGAA[C/G]GGTGAAGCAGTTAGA	54476
rs759292104	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5695591	AAGTTCTATTGCCCT[G/T]TTATGGTAGAAAAAT	54476
rs759297438	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5659784	TACTTCCTGAAACAA[A/G]GTGTGCCAACACCAA	54476
rs759300832	snp	C/G	3.30398e-05	0.00406434	intron-variant	RNF216	GRCh38.p7	7:5716695	AATGCCCAGAATAAA[C/G]AAGGTGAGATTTCAA	54476
rs759313241	snp	A/G	1.91834e-05	0.00309698	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5730748	GGCCAGCAGACTGCT[A/G]CTGGGATTTATAATG	54476
rs759326740	in-del	-/G	5.1917e-05	0.00509469	intron-variant	RNF216	GRCh38.p7	7:5741819	GGTTTATTTGTCTAA[-/G]GAAAAAATGAAATTT	54476
rs759343490	in-del	-/TT			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670461	TGGGTAAAAAAAGTC[-/TT]TTACTTCCTCTTTTT	54476
rs759353250	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5766070	GGGAGAATCACTTGA[C/T]GCTAGGGGTTCAAGA	54476
rs759354354	snp	A/G	1.82267e-05	0.00301878	intron-variant	RNF216	GRCh38.p7	7:5730674	ACAACAAAGCACAGC[A/G]TTTCCAGGCAGTGAC	54476
rs759355409	snp	G/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675908	GAGACGGGGTTTCTC[G/T]ATGTTGGTCAGGCTG	54476
rs759397328	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5694642	AAGGATGAGGCCCAC[C/T]TGTGGCGCAATTTGA	54476
rs759403122	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5769611	CACCTGTGGTACCAG[C/T]TACATGGGAGGCCGG	54476
rs759403134	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5717282	TACTTGAACCTGGGA[A/G]GCAGAGGTTGCAGTG	54476
rs759407259	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5661689	AAGTCTATAATCCCA[C/G]CTACTTGGGAGGCTG	54476
rs759415961	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5778301	TAAACTACTCTTCTT[C/T]ACTGCCTCTTGGACC	54476
rs759446723	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5778735	TTCAGCACCTCAGTT[C/T]CTTTTTTTAAAATTA	54476
rs759447796	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5658217	TGGGATCTACGTCTT[-/A]AGTGAAACGCTTTTC	54476
rs759477958	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5689241	GGCCTGGCTCCAGAA[A/G]CTGATATGGCAGCAT	54476
rs759484197	snp	G/T	1.73812e-05	0.00294793	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739356	AAATCTTGCTTCCTA[G/T]AAACAAATAAGAACA	54476
rs759485765	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681063	GACCCTTCCCACACT[A/G]GGGTCTCAGCTCCTG	54476
rs759494508	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5744165	TTGAGAACTGCAGCC[A/G]AGAAGAAGAAGAATC	54476
rs759500393	snp	C/T			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620092	AGTCCCAGTTACATA[C/T]GATACAGGCTTTTTA	54476
rs759507862	snp	A/G	1.65806e-05	0.00287924	synonymous-codon, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712782	CATAGTACTTATACA[A/G]GATGGTCTGGGGGAG	54476
rs759514977	snp	C/T	1.65029e-05	0.00287248	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712702	AGATGGCACGCTCTG[C/T]CTGAGAACGAACCTG	54476
rs759522664	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754881	ACAAATACAAAAATT[A/G]GCCGGGTGTGGTGGC	54476
rs759524594	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5704649	TCATGGAGCATCTGT[A/G]CCACCTAGTGGCAAC	54476
rs759537105	snp	C/T	1.6473e-05	0.00286988	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741625	TCCAGAAATTCACCG[C/T]AGTCATCCTCAGAAT	54476
rs759552295	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5715039	ATACATGGGACATAT[A/T]ACACAGTTCTTACCT	54476
rs759555543	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5680316	CTAGCTCTGTCATCA[C/T]AGAATGCGATCCACT	54476
rs759559112	snp	C/G	1.64811e-05	0.00287059	missense	RNF216	GRCh38.p7	7:5725379	TTGTTTTCTCTTCTT[C/G]CTTTTTCCACTGGTT	54476
rs759562703	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5696457	ACTAAAACAAATTCA[C/T]TGGCCGGTGGGAATG	54476
rs759597276	snp	C/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768097	AAAAAACTTAAACCA[C/T]AATGGAGGAGTATCA	54476
rs759603641	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671476	TAAATGAGGCTGATG[A/G]GGTGAGCGCTATTCC	54476
rs759608613	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5748190	TCTGATGAACTACTA[C/T]ATATAGATCTTAAAC	54476
rs759698845	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5735953	CAAAAATTAGCCAGA[C/G]ATGATGGCGCATGCC	54476
rs759704278	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5704666	CACCTAGTGGCAACT[C/T]GTTCCACAGCCCACA	54476
rs759708656	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5734948	TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC	54476
rs759726346	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753858	AAATTAGCCATGCGT[A/G]GTGGCGCATGCCTGT	54476
rs759745566	snp	A/C			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620521	GAGGGGCCTGGAGAA[A/C]CAGGGTGGGTGCTCA	54476
rs759747146	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665119	CACAAAATTCTAACA[C/T]GAATTCTTCTAACAG	54476
rs759756323	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665333	CCCCCACCTCACTCC[C/G]TAGTCCTGAGGAAAG	54476
rs759757401	snp	A/G	1.94797e-05	0.00312081	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712893	AAAGGCAAAGAAAAA[A/G]AAATCAATACCATTT	54476
rs759762334	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5685040	CCCAGGATTCTTGCT[C/G]ATGGTGAGCCACGCT	54476
rs759779248	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664593	AGAGAACTTCTGGTT[C/T]AGAGGGGTCAGGACT	54476
rs759805072	snp	C/T	1.64738e-05	0.00286995	missense	RNF216	GRCh38.p7	7:5641239	CAGAAATGGTCATAT[C/T]CATTAATAGAAACTC	54476
rs759817541	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5654063	GTCTTTTAAAAAAAA[C/T]CATTCTGGGTGGAAA	54476
rs759855634	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5629920	ATAAGATACTTCTTG[C/G]ACTTGGGATAAGTGA	54476
rs759873163	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5644044	TTTTTATGGTTGGAT[-/A]AATATTCCATTGTAT	54476
rs759901140	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5633990	AGAAACTATGAGTGA[C/T]TAAAAAGGGGAAAAG	54476
rs759912950	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5744908	ACCTGGGAGGCAGAG[G/T]TTGCAGTGAGCCAAG	54476
rs759946689	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5708794	GTAGGTTGGGTTCTG[C/T]CAGCAGTGAGTTGGG	54476
rs759983145	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5766392	TCCTATATTGAAGCT[C/T]TGACCTCCAATATAA	54476
rs759986740	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5702068	TCTGAGGCCCCAGGT[C/T]GCTGCCGGGTTCTCG	54476
rs759992948	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5746591	TGAGTCAGATGGAAA[C/T]TGCAAAGTGATTGGC	54476
rs759994976	snp	A/G	5.4807e-05	0.00523455	missense, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711772	CTACCTTTCGGCAGT[A/G]AGGATTAGGACAGCT	54476
rs760012625	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5735219	CTAAAGTCGTTTCAA[A/G]CTGACACTGCCCTTG	54476
rs760013854	in-del	-/AA			intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5780144	AGGAGTAACAGCTTG[-/AA]AACAATACATGGCAT	54476
rs760021344	in-del	-/C			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680778	TCTGGCCCCTGGGCT[-/C]CCCCTGTATCCCTGA	54476
rs760026704	snp	A/T			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622806	GGGGAGGGTTCTCCA[A/T]CCACACTCCTACCCC	54476
rs760035443	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5742175	CCTCAGCCTCCCAAG[C/T]AGCTGGGATTACAAA	54476
rs760070924	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5755849	CATATGCTCCATTTT[A/G]GCAGATAACACTAAA	54476
rs760072440	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5642086	CATTGTCAAGGAGAT[A/G]AGGTTTAGATAAAGT	54476
rs760083303	snp	A/C	1.64746e-05	0.00287002	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741111	ATCACTTGCTAACTG[A/C]TGGTCTTCAAACTCT	54476
rs760106512	snp	C/T	0.000164891	0.00907846	missense	RNF216	GRCh38.p7	7:5622970	TGGGCAGAGGGGGCA[C/T]GTACGGGGCTGGGAT	54476
rs760108788	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5693529	GACATTTGAGGAAGG[A/T]AAGAGCAGGAACTAG	54476
rs760114924	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5683550	ACCACCTCATCAGAA[C/T]TCTCTGAACAGGTAA	54476
rs760142030	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5775214	ATTTTCTTCAGTTAT[C/G]AAGTATTGCCCATTA	54476
rs760168672	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5727725	GAGAGAGAGACCCTG[C/T]TTCTAAACAAGAATA	54476
rs760180223	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5776068	TTGTAAGTCTGTACT[A/C]ATACAATTAATATTA	54476
rs760210712	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5726597	GCGCGGTGGCTCACG[A/C]CTGTAATCCCAGCAC	54476
rs760212462	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5775010	CGACACTCACCAAAG[C/T]GGTGAGATTACAGTC	54476
rs760239846	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5741965	CATTTATCTTAACAC[C/T]GAAATTTGATTACAC	54476
rs760244555	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5777241	AGAGAAAAATGGCCC[A/G]GGTGAGCACTTCTCA	54476
rs760280926	snp	A/C/T	9.15417e-05	0.00676491	intron-variant	RNF216	GRCh38.p7	7:5623202	GGATGTGGGGATTAG[A/C/T]GGAGAAAAACATTAA	54476
rs760297983	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5624639	CCTGGGCCAGGCCTC[C/G]GGGAGAGGAGGAAGG	54476
rs760304810	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5625198	CGGCTCAGCAAGCAG[C/G]AAAGAGATAGCTGAC	54476
rs760333116	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670909	AAGGCAGGACTCAAG[A/G]TCTTCCCAAGACGAA	54476
rs760339546	snp	C/T	1.75588e-05	0.00296295	missense	RNF216	GRCh38.p7	7:5624070	CCTCCATTCTTTCTT[C/T]TCTGTTCCTCTTCAG	54476
rs760342593	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5771007	GAGACAGGGTTTCAC[C/T]ATGTTGGCCAGGCTG	54476
rs760344096	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5750086	CTTATTTTTATGGCA[A/G]TATCATTATTTGCAT	54476
rs760360418	snp	C/T	1.67668e-05	0.00289537	intron-variant	RNF216	GRCh38.p7	7:5641135	CTATAAAGCAATAGG[C/T]AGCCATGTGTCTACT	54476
rs760375750	snp	C/T			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622554	TGTGAGCAGCAGGGA[C/T]CTGGTCTATGGCCTA	54476
rs760382572	snp	C/T	4.20884e-05	0.0045872	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5711913	AGCTCCATGTGGCTG[C/T]TCATATGAAGATGGA	54476
rs760390754	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5689113	ATGGCACCACCATCA[G/T]TGCCTTGTGAGCCAA	54476
rs760391937	snp	C/T	3.30131e-05	0.00406269	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712695	AGTTGGCAGATGGCA[C/T]GCTCTGCCTGAGAAC	54476
rs760395206	snp	A/G	1.80922e-05	0.00300762	intron-variant	RNF216	GRCh38.p7	7:5730666	CAACAACAACAACAA[A/G]GCACAGCATTTCCAG	54476
rs760409877	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5687459	TTAAGGGGACATGAT[A/G]TGGGATTTTCAGAAA	54476
rs760431567	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5643432	GGGGCAGGACAGGAA[A/G]AGAAGCCGGAGCTGT	54476
rs760432932	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5720780	GAGCGAAATGGAACC[A/G]AGGCTGAGGGAGGAG	54476
rs760434075	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5740633	CCATATTGGACAGCA[C/T]AGGTCTAGGTAATTC	54476
rs760450229	snp	C/G	1.64743e-05	0.00287	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741344	ACCAGCAGTCTTCTT[C/G]GATGGCCTGATCATC	54476
rs760503249	snp	C/G	1.6473e-05	0.00286988	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741266	GCTGCCGTTCCTGAG[C/G]AACGACCTGGTTTGT	54476
rs760510101	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5661723	CATGAGAATCGTTCG[A/T]ACCTGGGAGGCAGAG	54476
rs760523791	in-del	-/CAATGA	3.29451e-05	0.00405851	cds-indel, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741514	TGGGGTTGACAATGT[-/CAATGA]CATTTGCTGCTTGGT	54476
rs760589558	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5696562	GCAGCCTCCTAGACA[C/T]GCGTGCCCAAGATCG	54476
rs760590171	snp	A/T	2.72305e-05	0.00368979	intron-variant, nc-transcript-variant	RNF216, MIR6874	GRCh38.p7	7:5711886	TCAAACATTAAAGCC[A/T]GATCTGGTTCCAGCT	54476
rs760611796	in-del	-/T	0.00027843	0.0117956	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712897	GCAAAGAAAAAAAAA[-/T]CAATACCATTTATAG	54476
rs760626929	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5731520	CTGATGTATCACCAC[C/G]CAGACCCAACACATG	54476
rs760627066	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5636890	ACAAGGAAAAAGCAC[A/G]TGAGAAACCCACACC	54476
rs760641641	snp	A/G	1.65899e-05	0.00288005	intron-variant	RNF216	GRCh38.p7	7:5721197	ATACGACAATGCAAA[A/G]GCATGCAGACAACTA	54476
rs760653831	in-del	-/G			intron-variant	RNF216	GRCh38.p7	7:5626294	TAACTCAAGAGGGTT[-/G]GGGTGGGCAGTTTGA	54476
rs760657050	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5744344	AGTAAGGCATAGACA[A/G]AATGCAACATTAGAT	54476
rs760658129	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5695702	TAGTGTTCTCCCCTA[A/G]TCATCCTCGGATGGA	54476
rs760661468	in-del	-/A/AA			intron-variant	RNF216	GRCh38.p7	7:5776905	ACTCTGTCCAAAAAA[-/A/AA]AAAAAAAAAAAAGAG	54476
rs760667796	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5633233	CACCCGCCTTGGCCT[-/C]CCCGAAGTGCTGGGC	54476
rs760685458	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5690632	TAACCCTAAATAGTA[A/G]GCAGGACTGGCACTG	54476
rs760687491	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5706747	GCCTTTTCACTCTGT[C/T]GATGGTTTCCTTTGC	54476
rs760701304	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671533	GAGAGAGCCGGGCAC[A/G]GTGGCTCACGCCTGT	54476
rs760709107	snp	C/G	3.29451e-05	0.00405851	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741528	GTCATTTGCTGCTTG[C/G]TTATGACTCGGTCCA	54476
rs760709894	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5758084	CAGAGTATACATACT[C/T]GTCTAACAAAATATA	54476
rs760736849	snp	G/T			intron-variant, nc-transcript-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662534	GGTCGGTTTTGTTCA[G/T]AGCAATGCAGGTAAC	54476
rs760761787	snp	C/T	1.64727e-05	0.00286986	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741427	TCGGATGACTGGTTC[C/T]GAGTTTCCAAAGGAT	54476
rs760776566	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682117	AGGCACCTGAGGCCA[C/T]GCGGGCCCACGCTGC	54476
rs760785708	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5689363	CATATTTGTAGTATT[-/A]AAAAAAAAAAAAAAA	54476
rs760785905	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667613	TCACTTGGGCAGAAA[C/T]AAGCCAGGCTGACCT	54476
rs760792168	snp	A/C			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754068	TGACGCACCTCATCA[A/C]TGCAATTTTTGAAAT	54476
rs760810222	snp	C/G			utr-variant-3-prime	RNF216	GRCh38.p7	7:5621536	CCCGCCTGCCCCAGG[C/G]ACCTTGGGTGGGCCA	54476
rs760823895	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5724610	TCACAGCCTAAGGGA[C/T]TTTCTTTTAGAGCCT	54476
rs760878490	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5779118	TTATGTCTCTAAAGA[C/G]CTAGAATATAGCAAT	54476
rs760887806	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5705678	CTTTGGGAGGCCAAG[A/G]CAGGCAGATCACCTG	54476
rs760891064	in-del	-/CTTT			intron-variant	RNF216	GRCh38.p7	7:5710863	CACGCTAGCACTCTG[-/CTTT]CTTAAGAGCTGCAAG	54476
rs760931090	in-del	-/TAC			intron-variant	RNF216	GRCh38.p7	7:5745150	TCCCCAGCAGCACAT[-/TAC]TACTACATTACAATG	54476
rs760940487	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5629936	ACTTGGGATAAGTGA[C/T]AGATGGGGTATTGAG	54476
rs760981957	snp	A/C			upstream-variant-2KB	RNF216	GRCh38.p7	7:5783604	TTCCTTCTCTAAGAC[A/C]GTAGAGTGTGGCTTA	54476
rs760993536	snp	A/G	1.6916e-05	0.00290822	intron-variant	RNF216	GRCh38.p7	7:5725481	TTCTGTAAATAGAAA[A/G]TAAGAATACACGAGA	54476
rs760994579	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5714197	CGAACTCCTAATCTT[A/G]TGATCCACCCAACTT	54476
rs760995539	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5644305	TCCCACCTCAATGTA[C/T]ACTGGTGTCATTTTT	54476
rs761015202	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5764311	AAAACCACACATAAA[A/G]ATGTCATAAGGTAGA	54476
rs761020190	snp	A/T	1.6477e-05	0.00287024	missense	RNF216	GRCh38.p7	7:5761047	AAGTGAATTACCTCT[A/T]CATTGTTGTTTCCCT	54476
rs761048757	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5709583	CACAAGAAGCTACAT[A/G]GCTACCTTCAAGTTC	54476
rs761048838	snp	A/T	1.6476e-05	0.00287014	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741094	GGACCTGGCTCTTCA[A/T]CATCACTTGCTAACT	54476
rs761061630	snp	C/T	0.000230878	0.0107418	intron-variant	RNF216	GRCh38.p7	7:5652541	AGACACAAAGACAAC[C/T]CCTGGTGAGTGGACA	54476
rs761069998	snp	C/G	3.2963e-05	0.00405961	missense	RNF216	GRCh38.p7	7:5725399	TTCCACTGGTTTCTG[C/G]TGACAGCTCCTGCCA	54476
rs761073821	in-del	-/AAG			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767038	ACAGCTAATCCTAAC[-/AAG]AACCCTATAATCCTG	54476
rs761088991	snp	C/G	1.6492e-05	0.00287154	missense	RNF216	GRCh38.p7	7:5622963	CGCACGTTGGGCAGA[C/G]GGGGCACGTACGGGG	54476
rs761109424	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5757021	TCATAAATGTAATAG[A/G]CTACATTTTCATTAT	54476
rs761114493	snp	A/G	3.29843e-05	0.00406092	intron-variant	RNF216	GRCh38.p7	7:5716780	TGCTGAAGAACAAAA[A/G]AGGCACACATTCAGA	54476
rs761129937	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5755486	ATTTCTAGCACATTA[A/G]TAGCCCCCTTGTGCT	54476
rs761130065	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5649698	ACTTCTAAGATGCAG[A/T]GGCGATGATTCTTTC	54476
rs761143303	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5653600	GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	54476
rs761147492	snp	C/T	0.000166138	0.0091127	missense, intron-variant	RNF216	GRCh38.p7	7:5741787	GCTGGTTTGATGAGA[C/T]TGGGTCGTGATCTCT	54476
rs761155556	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5638033	CAGCCCCCTTGGATG[C/G]GCCCCACACCCTCTC	54476
rs761174522	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5723443	ACGAGGTCAGGAGAT[A/C]GAGACCATCCTGGCT	54476
rs761202374	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5625453	TGGATTTTTTCATGC[C/T]GATCTGATGACACCC	54476
rs761203962	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5773026	CTCTGGTGATCCACA[C/T]GCCTCAGCCTCCCAC	54476
rs761222819	snp	C/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767708	GGTTCAAGCCATTTT[C/T]CTGCCTCAGCCTCCT	54476
rs761233063	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5761373	GAGAAATGACATCTT[A/G]ATACAAATATGCTAA	54476
rs761233566	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674813	CCAGCCTGACCAACA[C/T]GGCAAAACCCCATCT	54476
rs761264228	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5773966	TTACAGCTAATTTAG[C/T]TGAAATGTCAGGCTT	54476
rs761271927	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712392	GCATGAGAATTGCTT[A/G]AACTCAGGAGGCGGA	54476
rs761324294	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5649067	ATTTGCTTGAAAACA[C/T]TATAGCAGTTTAAAA	54476
rs761349870	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669099	TGGCCCCCCTTGGTG[A/G]AAACTATCCCACCCA	54476
rs761410372	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5684592	TGGCTGATGTCAGGG[A/G]CAGTAAAGCCCATCC	54476
rs761415654	in-del	-/TCTT			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673849	AGACCTCCATCTCTC[-/TCTT]TCTCTCATTTTTTTT	54476
rs761427211	in-del	-/A			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674996	GAGAGACTCTGTCTC[-/A]AAAAAACAAACAAAC	54476
rs761433343	snp	C/G	4.94181e-05	0.00497057	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741190	TGCTGGGGTTCCGGC[C/G]TTGGAAAAGCGGGCC	54476
rs761448480	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5703406	ATCACAGCTGGAGCT[A/G]CCCTGGCATTGATAG	54476
rs761456094	snp	A/G	1.65203e-05	0.002874	intron-variant	RNF216	GRCh38.p7	7:5721175	ATTTTTATGTCACCT[A/G]GAAGATATACGACAA	54476
rs761468526	in-del	-/G			intron-variant	RNF216	GRCh38.p7	7:5693416	CCTCCACTGTACTGA[-/G]GGTACCAAAATGTAC	54476
rs761469213	snp	C/T	1.79271e-05	0.00299386	missense	RNF216	GRCh38.p7	7:5623164	AGCGGGGGTCCAATG[C/T]GTTTGAAGGTGTTCT	54476
rs761498986	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5750973	AAGTATTGCAGAGCA[A/G]ACTACTTGGTTAAAA	54476
rs761522435	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5658756	AAATTTTCTGTATCT[C/G]TGTATGTTTTGCCAT	54476
rs761527954	snp	C/T	5.04223e-05	0.00502082	missense	RNF216	GRCh38.p7	7:5623099	GCAGGTTCTGCGGAA[C/T]GGGCCTCGGGAGGGC	54476
rs761547211	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5742881	GATTACAGGTGTGGG[G/T]CACCGCGCTTGGCCG	54476
rs761577119	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5728349	CTGTGGGAGGCTGAG[A/G]TGGGCAGATCATCTG	54476
rs761586025	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5627354	GTGAGGAGTGTGGCA[A/G]CCTTGGCCCTCCTTG	54476
rs761596456	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670123	ATTTTTAGTAGAGAC[A/G]GGGCTTCACCATGTT	54476
rs761606720	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5730458	AGATATGGAGAATTC[A/G]TTCAATTCTTTGTGG	54476
rs761607696	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5634068	CAGGCTGACTGTTCC[C/T]AAAATAACCATTTGA	54476
rs761610775	snp	C/T	1.72961e-05	0.00294071	missense, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711801	CTGAACCTCTTCACA[C/T]CACTGTCCAACAGAG	54476
rs761643221	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5702122	CCTTGGCTCTGAAAT[C/G]CAGGTGGGTGTGGGC	54476
rs761647081	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5771904	AAATAAATGAAAAAG[C/T]GTCCAACATTATGAG	54476
rs761653831	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679435	GATGCAGGCGCTGAG[C/T]GCACTGGTGCACACA	54476
rs761666855	snp	A/C	1.6569e-05	0.00287824	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752907	TGAGGAGCTGGGGTG[A/C]CCAGCATTGGAATCC	54476
rs761675851	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5626845	GCTCAAGTATGTAAA[C/G]GATGTAGCCCAAAGT	54476
rs761689911	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5775543	AAGACTTTCAAATTT[A/G]ATGAGTTAATCCCTT	54476
rs761700234	in-del	-/TACA			intron-variant	RNF216	GRCh38.p7	7:5748611	TATTTTTTATATACA[-/TACA]CACACACACACACAC	54476
rs761732700	snp	A/T	1.71472e-05	0.00292802	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739329	CTCAATAAACCCATT[A/T]GCTACATCTGGAAAT	54476
rs761744052	snp	A/T	1.65935e-05	0.00288036	missense, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712788	ACTTATACAGGATGG[A/T]CTGGGGGAGCACCTT	54476
rs761745997	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780867	GCACGCTCCAGGGTT[A/G]GTTGCAAGTGGCCCA	54476
rs761750117	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5706971	AGATATGGTATCAGC[A/G]TCTAAGTTCATTCTT	54476
rs761758021	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5759045	GTATTTCATAAATGA[C/T]TTAGCACAATCCGTT	54476
rs761762184	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663350	CTTTGGGAGGCCGAG[A/G]CAGGTGGATCATGAC	54476
rs761803147	snp	C/T	1.64727e-05	0.00286986	synonymous-codon	RNF216	GRCh38.p7	7:5721075	ATAGAACTCCTGCTC[C/T]TGTTGCACAGCTGGA	54476
rs761805444	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662656	GCCGCTGAGAGCCTT[C/T]CATCAGTGCCAGAGA	54476
rs761812574	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5719617	ATCAATTTGCCAATA[C/T]TTTAAATACTTATCT	54476
rs761826343	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5697668	AAAGGTTTTGATGGA[A/G]TCCAGAGACAGAAGG	54476
rs761833627	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5710890	CTGCAAGATGCCAGC[A/G]ACTGTTGTGACAATT	54476
rs761838953	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5687675	CAGAGAAATTAAGTG[C/T]CCCCAAATGACCAGG	54476
rs761842163	in-del	-/AG			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780882	GGTTGCAAGTGGCCC[-/AG]AGTCTTGGATCCCTG	54476
rs761845967	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5750406	TCAAATATGTGGTTA[G/T]TCAGGCAAACTGGTC	54476
rs761847598	snp	G/T	1.64768e-05	0.00287021	missense	RNF216	GRCh38.p7	7:5761028	ATGGCAGTGAAAGTT[G/T]TTCAAGTGAATTACC	54476
rs761876529	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5652743	GGAAGGCTGTGGCAG[A/G]CCAGGAGTTTGAGAC	54476
rs761888397	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673388	GAAAGCATCTACAAG[A/G]ACAGGCAGGCAGGTG	54476
rs761916861	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5779262	TTCTTTATCAGATTT[A/C]TCCACAGGGGCTTCA	54476
rs761920023	snp	C/G/T	6.59918e-05	0.00574388	missense	RNF216	GRCh38.p7	7:5622952	CATAGTTGACCCGCA[C/G/T]GTTGGGCAGAGGGGG	54476
rs761935230	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5739153	TGATAGTTGCATAAT[A/G]ATGTGAATTTACTTA	54476
rs761961260	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5766504	CTCTGAGAAGAAGAG[A/G]TCTAGAGAGCTTGCT	54476
rs761962683	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5699297	TGAAACTAATGCAGC[A/T]TATCAAAATTACACC	54476
rs761996445	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682188	CAAAGTTGGCAGATT[C/T]TGTACCTACGTGCCA	54476
rs762021113	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5771207	ACTCAAAAGCCATAT[A/G]TGGGGTGGGAGTAGG	54476
rs762022660	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5696560	GGGCAGCCTCCTAGA[C/T]ACGCGTGCCCAAGAT	54476
rs762047981	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5645966	AGTTCTTTGCCCATG[A/G]TTTCACCTGGCTTTC	54476
rs762067228	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5757546	GAGTAGGTAAAAACA[C/G]TATTTAGCAATTAAA	54476
rs762069464	snp	C/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754276	TCCTCCCATGTCAGC[C/T]TCCCAAGTAGCTAGG	54476
rs762075981	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5657477	GAGGCTGAGGCAGGA[C/G]AATAGCTTGAACCCA	54476
rs762081232	snp	A/G			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620835	AGGGTACAGGGCAGA[A/G]GGAGCTGAGGCTCCC	54476
rs762093339	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5631923	GGATTGCTTAGCTCA[A/C]ACCCCCTTCTCCACG	54476
rs762098589	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5705866	GAGCCAAGATCATAC[A/C]ATTGCACTCCAGCCT	54476
rs762099212	snp	C/T	3.29478e-05	0.00405867	missense	RNF216	GRCh38.p7	7:5652414	ATTCTGTTACTCACA[C/T]AGAGGTACGGTACTT	54476
rs762099941	snp	C/G/T	3.29904e-05	0.00406132	synonymous-codon, missense, intron-variant	RNF216	GRCh38.p7	7:5741719	ATTCAAATGCTGCTC[C/G/T]AGACTTTTTAGGCCT	54476
rs762125060	snp	A/G/T	3.29632e-05	0.00405964	missense	RNF216	GRCh38.p7	7:5725392	TTCCTTTTTCCACTG[A/G/T]TTTCTGGTGACAGCT	54476
rs762130180	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5724802	CAGATAAAATCTGAG[C/T]TGTTATAACACTCAA	54476
rs762130262	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5727425	TTTAGTCCTCATCTT[G/T]CACAAACTCTTAGCA	54476
rs762137602	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5635967	ACAAAGACACTGTAG[A/G]AAACAATTCTCTGTA	54476
rs762177929	snp	C/G	1.67992e-05	0.00289816	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741005	GTTCAACGAGCTCTT[C/G]ATCTACCTCTGCAGC	54476
rs762191947	snp	A/C			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676757	AGAAAGAAAACTCCT[A/C]AACATACAGTGCAAC	54476
rs762218461	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5700797	TGAGCAGCCCTGGCA[A/T]CCAAGCCTGCCCGCT	54476
rs762220060	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5726204	ATCACTTGAGCCTGA[C/G]AGGCAGGGTTGCAGT	54476
rs762232959	snp	A/G	5.67167e-05	0.00532495	intron-variant	RNF216	GRCh38.p7	7:5740926	AAAAAAAAGAAAAAA[A/G]CTCAGTATATGTAGT	54476
rs762250191	in-del	-/AAG			intron-variant	RNF216	GRCh38.p7	7:5688454	GTTGACACTAGTGAA[-/AAG]AAGAACACATACTGA	54476
rs762266442	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5691403	ATTGCTCCAGGCCCA[C/T]TAATGATACAAGAGC	54476
rs762273759	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5763486	AATATAAAAATTAGC[A/C]AGGCGTGGTGGCAGG	54476
rs762281379	in-del	-/G			intron-variant	RNF216	GRCh38.p7	7:5630246	TCTTCAAGAGAGGCT[-/G]GCTGGCGTCACGGGA	54476
rs762287634	snp	C/T			downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620040	GGTGGAGAGACGAAG[C/T]TGGAGGGAGCAGAGC	54476
rs762293134	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5715433	TTCTGGTATTCTTTA[C/G]AGTAATTCTTTATAT	54476
rs762295333	snp	A/C	1.77944e-05	0.00298276	intron-variant	RNF216	GRCh38.p7	7:5641391	ACTGAAATAAGAAAA[A/C]ATAATTTGGAGCTGG	54476
rs762334231	snp	A/G			intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739448	TATAATAAAATGACT[A/G]AAGACTAGAAAAGGG	54476
rs762342656	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5737567	AATAAATATAAATCT[A/G]ATGACAGTGGTTGCC	54476
rs762357498	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5757885	GTTGGCCAGGAGCAG[C/T]GGCTCACACCTGTAA	54476
rs762358977	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5640875	GATACATGTGTAAGT[C/T]TCCTTACTTTGCTCT	54476
rs762360929	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5630944	CTCAGGTTTCTGAAT[C/T]GGAACTTCTGGCAAA	54476
rs762373114	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5635416	ACTCTTTTGTAGAAT[-/A]AATTTTTAAGGTTAA	54476
rs762404784	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5710653	CCCTACTCAGCTTAT[A/G]AGCCTCCTTCACACT	54476
rs762411204	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5760427	AGGCTCAGACCGGAG[-/A]ATCATTTGAACCCAG	54476
rs762417899	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5759191	CTTCTGTCATGATTG[-/T]TAAGTTTCCTAAGGC	54476
rs762438805	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673948	TCACTGCAACATCTG[C/T]CTCTTGGGCTCAAGT	54476
rs762458855	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5764703	AAAGTAATAAAATAT[C/G]ATCTTTAGGTAGTAG	54476
rs762464461	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5747159	GTTTCCTTATAAAAC[A/G]GAACAACCTGAAAAT	54476
rs762464972	snp	G/T	1.64738e-05	0.00286995	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741138	CTCTCCTAGAGGATG[G/T]GCAGGCTGAGGAGAA	54476
rs762470770	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5627019	TGCACAACCACCACT[-/C]CTGCCTCACCTCAAC	54476
rs762470825	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5685553	ATCAAGGCAAATTCT[A/G]TTACTTTTTCCTCTT	54476
rs762476962	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5643296	GATGTGGTGACTACC[C/T]AGCCAGTAATATAAA	54476
rs762483308	in-del	-/G			intron-variant	RNF216	GRCh38.p7	7:5756154	GGTTTTATATGCACT[-/G]GCATTTCCCCTGCTT	54476
rs762486566	snp	A/G	1.93497e-05	0.00311038	intron-variant, nc-transcript-variant	RNF216, MIR6874	GRCh38.p7	7:5711856	TAGAGTCAGAACAGC[A/G]GAACTGACATTACTT	54476
rs762487101	snp	C/T	3.29457e-05	0.00405854	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741186	ACCTTGCTGGGGTTC[C/T]GGCCTTGGAAAAGCG	54476
rs762492956	snp	A/G	1.65056e-05	0.00287272	missense	RNF216	GRCh38.p7	7:5623051	GGGGGAAGGGTGGGT[A/G]CGCGAAGGCATAGGG	54476
rs762509508	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5748526	GGATTATAGGCGTGA[A/G]CCACCGTGTCCAGTT	54476
rs762518586	in-del	-/T	1.87601e-05	0.00306263	intron-variant	RNF216	GRCh38.p7	7:5752825	AATAATGTCTCATTG[-/T]TAAGTTTAAAGAAAA	54476
rs762536124	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5650320	AATAGGACCCAGTGG[G/T]GGGCTATGTGTGGCA	54476
rs762548856	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5657966	GGCTTGGTCCTTGCC[C/G]TCAAGGAGTGCACTC	54476
rs762576658	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5694722	GCCTATGGAAAGTAC[A/G]TTCTCTGTAGCTGCG	54476
rs762582176	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5629728	ACTACTCGGGAGGCT[C/G]AGGCAGGAGAATCAC	54476
rs762595099	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675578	GCCCAGGAGGTCGGG[C/T]TGCAGTGAGCTAGGA	54476
rs762596632	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5709617	AGGCCATGTATATTC[C/T]TCCCATAGACAAACA	54476
rs762604400	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713798	ATGAGGCATTTACCA[C/T]GTGTCAAACAATAAG	54476
rs762610415	snp	C/T	3.42237e-05	0.00413651	intron-variant	RNF216	GRCh38.p7	7:5730866	TTCCAAATCCCACAC[C/T]TGCCCATTGCTTCAA	54476
rs762613913	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5771993	AATCCCAGCACTTTG[A/G]AAGGCCGAGGCGGGT	54476
rs762628971	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5623870	AAACTATATTCAAGG[C/T]GTTGAAGGCCTTTCC	54476
rs762645430	snp	C/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767745	TGGGGACTACAGGCA[C/G]ACGCCACCATGCCCA	54476
rs762646861	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5644016	TGTTGTAGCATGTAT[C/T]GATACTTCATTCCTT	54476
rs762654733	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5765787	TCTCTACTAAAATAC[-/A]AAAAAAAAAAAAAAA	54476
rs762660164	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5649869	GCAACTGGTATGCTG[C/T]GAATGATTTGGAAAA	54476
rs762663731	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5773246	TTTCCCCAAATAAGA[-/T]TTTTTTTTTTTTTTG	54476
rs762668188	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671176	GGCTCAGCAACTGCT[C/T]CATGTGCCCATGTGA	54476
rs762672429	in-del	-/T/TT			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666814	TACTACAGCAATGAC[-/T/TT]TTTTTTTTTTTTTTT	54476
rs762705099	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5718864	ACCCGGCCAAACTTA[A/C]GTTTTTTTAGTCTTG	54476
rs762705676	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5757100	CTGGGTGCAGAATCC[A/C]ACCTATGTTTATTAC	54476
rs762711660	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5777093	CACACAGAAAGACCT[A/G]ACACTACACGTGGAG	54476
rs762726769	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5729330	TAAATTCCTTAGCAA[A/T]CATAAACCATCCCAA	54476
rs762765001	snp	C/T	3.30153e-05	0.00406283	intron-variant	RNF216	GRCh38.p7	7:5716796	AGGCACACATTCAGA[C/T]ACAAATTTAGTAAAA	54476
rs762774752	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5693835	GCATGCAAAGACAGA[C/G]ATGGACGCGGGTAGA	54476
rs762780520	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5777674	TTCAGAGAAAGAAAA[C/T]GAAAATTGTGTTAAC	54476
rs762799674	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5634086	AATAACCATTTGAGC[A/G]CTTGGCACAAAACTA	54476
rs762812573	snp	C/T	1.95808e-05	0.0031289	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5730759	TGCTACTGGGATTTA[C/T]AATGATTCTGTCTTC	54476
rs762819460	snp	A/G	8.78835e-05	0.00662827	synonymous-codon	RNF216	GRCh38.p7	7:5624120	AATAAGCTTCTCATC[A/G]TCTTCCTAAAACGCA	54476
rs762819878	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5761644	TACAAAAATTAGCTG[A/G]GCGTGGTGGCACGTG	54476
rs762821807	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5751197	GAACAACAACAACAA[A/C]AAAAAGTGTGATAAT	54476
rs762844847	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5766784	AAACAGGGTCTTAAT[C/T]TCAAGTAACAAATGT	54476
rs762868908	snp	A/C			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670360	TGCAGAGGACCCAGC[A/C]ATGTGATAGTGGGCT	54476
rs762876119	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5744033	TTAATGCAGCAACAG[A/G]AAATCAAAACAAGAG	54476
rs762879867	in-del	-/TTTTTT			intron-variant	RNF216	GRCh38.p7	7:5715739	CACCAACTCATTCTT[-/TTTTTT]TTTTTTTTTTTTTTT	54476
rs762895166	snp	A/C	1.69931e-05	0.00291483	intron-variant	RNF216	GRCh38.p7	7:5725302	TGCAGCTACACACTG[A/C]CACCAACACAGTTTG	54476
rs762897049	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5720863	ATGAAACCACAAACA[-/T]TAAGTATTATGACAA	54476
rs762909026	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5721750	TGCAAATGTGCTGTA[G/T]GATTTTCAACCATTT	54476
rs762913196	snp	C/T	1.67391e-05	0.00289297	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753023	GGGAGGTTGGCACTA[C/T]CACATCCAACTCTTT	54476
rs762923746	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5770094	GCTCACGCCTGTAGT[A/C]CCACCACTTTGGGAG	54476
rs762939163	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5689207	TGGGGAGGTGGATGC[C/T]TGACGGGGGCAAAGG	54476
rs762948181	snp	A/G	0.000168251	0.00917045	intron-variant	RNF216	GRCh38.p7	7:5739635	CTCTGTCTAGACAAA[A/G]GGAATCCAAACACAA	54476
rs762951653	snp	C/G/T	2.25904e-05	0.00336076	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712910	AATCAATACCATTTA[C/G/T]AGAAAAATAAAAAGC	54476
rs762978438	snp	C/T			downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620015	GCCCCTGTAACTTGC[C/T]GGATGGCGGGGTGGA	54476
rs762980353	snp	C/T	1.74668e-05	0.00295518	splice-acceptor-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712865	CAGCTGAGCTCCAAC[C/T]AGAAAAAGGCGAAAA	54476
rs762983585	snp	A/G			upstream-variant-2KB	RNF216	GRCh38.p7	7:5782743	TAATCCGAGCTACTC[A/G]GGAGGCCGAGGCACA	54476
rs762990639	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5643190	AAATGTTAAACAGCT[A/C]TTCAATATTGCACAA	54476
rs762999540	snp	A/G	1.69189e-05	0.00290846	missense	RNF216	GRCh38.p7	7:5622882	CGATGCCGCGGCTGG[A/G]GGCCAAAGTGCATGG	54476
rs763012386	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5701861	GACAACTTACTATGA[A/G]AGCCCAGCAAAAGAC	54476
rs763014155	in-del	-/G	1.88372e-05	0.00306891	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712887	AGGCGAAAAGGCAAA[-/G]AAAAAAAAATCAATA	54476
rs763022460	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664569	GTAGACCCTGAAAAT[A/G]TGTGCCCAAGAGAAC	54476
rs763055905	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5633523	CAGGCTGCAGTGAGC[C/G]GAGATCACATCACTG	54476
rs763095260	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5735131	AGCCTGGGCAAGAGA[A/G]TGAGACTTCGTCTCA	54476
rs763119063	snp	A/C			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681915	CCCTAAGGGTGGTAA[A/C]CCCCAGTGGTTTTCT	54476
rs763135338	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5698991	AACCAAAACAATGAG[A/G]GCACAGATAAAGCTA	54476
rs763141457	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5721575	CGAATTGCTAGATCA[C/T]GGGATAGGCTTACTT	54476
rs763149369	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5722123	AGAGATGGGATTTTG[C/T]CATGTTGTCCAGGCT	54476
rs763152375	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5688580	TTTTGAAGAAAAAAG[G/T]TAAAGGCGCATGTAT	54476
rs763155936	snp	C/G/T			intron-variant	RNF216	GRCh38.p7	7:5708050	TAGTTCTCATACTTT[C/G/T]TGAATTTTCTTGCTG	54476
rs763156935	snp	G/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682234	TTCTCAAATCTAGAC[G/T]CCAAAAATCCCTATC	54476
rs763163615	snp	A/C			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768244	TCACTTGAGCCCAGG[A/C]GTTTAAGACCAGCCT	54476
rs763173252	snp	A/G	3.29473e-05	0.00405864	synonymous-codon	RNF216	GRCh38.p7	7:5641259	AATAGAAACTCGACA[A/G]AGGTAGCACATCTGG	54476
rs763200435	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673528	AAGCTGACCTGTCAC[A/G]TGGGGCAGTATGCAG	54476
rs763202402	snp	C/T	3.64651e-05	0.0042698	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622839	ACGGGCTTTGTGCTG[C/T]TCAATGGGGATTCGG	54476
rs763205415	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5746498	CAGGGAGGGTATAAA[C/G]TCAGGCTTTTGGAAT	54476
rs763229316	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5637068	GAAATACTGCCTGTG[C/G]AGCTCTTCATAGCTC	54476
rs763233175	snp	A/C			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753744	GCTCACGCCTGTAAT[A/C]CCAGCACTTTGGGAG	54476
rs763246874	snp	A/G	1.65051e-05	0.00287267	synonymous-codon	RNF216	GRCh38.p7	7:5715158	GAATGGAAATTCCCC[A/G]TAGCAGCAGCGACAC	54476
rs763263520	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5716662	GACAAAACATGGTAA[A/G]AGAAAACAGCCCATG	54476
rs763268708	snp	C/T	5.0531e-05	0.00502623	synonymous-codon	RNF216	GRCh38.p7	7:5641370	GGCAGCAGTCATTTT[C/T]TCTTCACTGAAATAA	54476
rs763271758	snp	C/T			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622669	CTCCACCATTTGGGA[C/T]GTCTTTATTATGGAT	54476
rs763284593	snp	A/C/T	3.591e-05	0.00423721	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739391	TTATATTTCATTCAC[A/C/T]AGAATGGTTTCAAAT	54476
rs763290628	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5746972	TTTTGAAAGATTAAC[G/T]GCAAAAAGCTAATGA	54476
rs763331679	in-del	-/ACAA			intron-variant	RNF216	GRCh38.p7	7:5656267	GAGCAAGATTCAGTC[-/ACAA]ACAAACAAACAAAGT	54476
rs763337085	snp	A/C/G			intron-variant	RNF216	GRCh38.p7	7:5727630	CTAGCTACATGGGAG[A/C/G]CTGAGGCAGGAGGAT	54476
rs763349920	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5693800	CTCTAAAGCTGGTCA[-/C]CCATGGCCAGGCAGC	54476
rs763381430	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5632296	AGTCTCTGTGCCTCA[C/T]CCTTGGTTTCTGGCA	54476
rs763396026	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5683304	TGCTGGATTTTGTTT[C/T]ATTTTTAAAGAGACA	54476
rs763399106	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5760804	CTTATTAATCCATTT[G/T]TAATGAATGAGTCTT	54476
rs763435330	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5657602	TAAAATGGTGAGACT[A/G]TAAATCTCCAGCACT	54476
rs763439593	in-del	-/TTC			utr-variant-3-prime, cds-indel, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620186	TAATGAACTAATCGT[-/TTC]TTGTTTTTATACAAA	54476
rs763447957	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5643433	GGGCAGGACAGGAAG[A/T]GAAGCCGGAGCTGTG	54476
rs763450375	snp	C/T	1.64974e-05	0.00287201	synonymous-codon	RNF216	GRCh38.p7	7:5715098	ATATCTGATGAGACA[C/T]TCTTTGCAGAACAAG	54476
rs763461674	in-del	-/A			upstream-variant-2KB	RNF216	GRCh38.p7	7:5782429	ATAACTGACTAAAAT[-/A]ACTGCTCCTGCTGGG	54476
rs763468998	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5632863	ATCCAATGAGTACCA[G/T]GACGAAGCACACGAA	54476
rs763501382	snp	C/T	4.94173e-05	0.00497053	missense	RNF216	GRCh38.p7	7:5729502	TGACTACTGAGCACT[C/T]TGAAGTCGGCCATGA	54476
rs763515140	snp	C/G/T	5.5157e-05	0.00525128	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622812	GGTTCTCCATCCACA[C/G/T]TCCTACCCCAAACGG	54476
rs763545525	snp	G/T			missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741085	GGAAAGGCTGGACCT[G/T]GCTCTTCATCATCAC	54476
rs763554942	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5691497	GCTATGGTGGGGGTG[A/G]GGAAGGCAGTGCTGG	54476
rs763558799	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669032	TAGTTCTGTGGACCT[A/G]ATATTATAAAGAGCA	54476
rs763585187	snp	C/G	1.66726e-05	0.00288722	missense	RNF216	GRCh38.p7	7:5623091	TGGCTGTGGCAGGTT[C/G]TGCGGAACGGGCCTC	54476
rs763588399	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5698025	GGCAGCTTTTGAAAC[-/T]TCAAATGCTTTTCAT	54476
rs763604028	snp	C/T	1.66001e-05	0.00288094	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752899	CATGCTGCTGAGGAG[C/T]TGGGGTGACCAGCAT	54476
rs763619417	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5755326	ACACAACACACCACA[C/T]GTAAGGTTCCAATTA	54476
rs763649384	in-del	-/TG			intron-variant	RNF216	GRCh38.p7	7:5728747	CAAAAGAAACATCAC[-/TG]TGTTTGCTGAGAATC	54476
rs763651978	snp	G/T			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622680	GGGACGTCTTTATTA[G/T]GGATCCGTCCACTCT	54476
rs763681048	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712026	TCTTATCAGGAAACA[C/T]AAGCACCACATGAGG	54476
rs763687899	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5702086	TGCCGGGTTCTCGGA[G/T]CCCACGCTGACTCTA	54476
rs763709421	in-del	-/CAT	0.000188626	0.00970965	cds-indel	RNF216	GRCh38.p7	7:5752860	CTTCTGTCAGGATGA[-/CAT]CATCATCCAGGTCCT	54476
rs763725706	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5764599	GTTGCAGTAGGCCAA[C/G]ATTGTGCCACTACAC	54476
rs763745683	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5701589	ATTGTACACGGAAAG[G/T]AAATGTGGCTTAGGG	54476
rs763753865	snp	A/G/T	3.29474e-05	0.00405867	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741139	TCTCCTAGAGGATGG[A/G/T]CAGGCTGAGGAGAAG	54476
rs763754969	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5683596	TTGTGATGGGAGAGA[C/G]GTGCCAGTTGCAATC	54476
rs763770441	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5632457	TGAGGTGAGAGGGAG[C/T]GGATGCTGATCAGCG	54476
rs763773743	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677023	ACATGAAACGAACCT[C/T]GTAAGAGAACTAACT	54476
rs763801197	in-del	-/AGT			intron-variant	RNF216	GRCh38.p7	7:5744557	CACAGATTAAGACAA[-/AGT]AGAACAACAGTCTGT	54476
rs763807693	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5740677	TAAGGGTTTCCATTT[C/G]GAGTGAACTCAAGGA	54476
rs763811947	snp	A/G	3.64904e-05	0.00427128	intron-variant	RNF216	GRCh38.p7	7:5752836	CATTGTAAGTTTAAA[A/G]AAAACTCACTTCTGT	54476
rs763827346	snp	A/C	1.65116e-05	0.00287324	intron-variant	RNF216	GRCh38.p7	7:5716799	CACACATTCAGACAC[A/C]AATTTAGTAAAAATG	54476
rs763848064	in-del	-/AGAG			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674979	TCCAGCCTGGGCGAC[-/AGAG]AGAGACTCTGTCTCA	54476
rs763861261	snp	C/T			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622208	TGACTTTCCAGAGAC[C/T]GAGGATGAGAAAGTT	54476
rs763864272	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5698688	CATGAGCCACCGCTC[A/C]GGCCTCTTGGATTCT	54476
rs763876984	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5711113	GCTTAGAGCGTATTT[A/G]TCTAGGTGGATGCTA	54476
rs763877846	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5758974	ATTTCATATTCAACT[A/G]TAAACCCCAATGTTG	54476
rs763895153	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5731871	CAGCTCTGCTCCTTT[C/T]CTCATCCAGGTGCCA	54476
rs763896590	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5742049	ATAGTTTGAATTATA[A/G]TTTATTTTTATTTTT	54476
rs763906664	snp	C/T	1.75693e-05	0.00296384	missense, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711787	GAGGATTAGGACAGC[C/T]GAACCTCTTCACATC	54476
rs763916901	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5651490	ACCTGCCTTAGCCTC[C/T]CAAAATGCCAGGATT	54476
rs763919400	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5758126	AGTAATTTTCCAAAA[A/T]GAATTAGTTGTTCTT	54476
rs763921283	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5658382	TTATTTTGGGCCGGG[A/C]ACAGTGGCTCATGCC	54476
rs763925722	snp	G/T			intron-variant, nc-transcript-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662553	AATGCAGGTAACAGA[G/T]ACAGTTTCTGCACTG	54476
rs763928511	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5687601	GTGACAAGCCTCTCT[G/T]CCTGCCCCTTGTGAA	54476
rs763928750	snp	C/T	1.64727e-05	0.00286986	synonymous-codon	RNF216	GRCh38.p7	7:5721066	TTTCTGCTCATAGAA[C/T]TCCTGCTCTTGTTGC	54476
rs763966855	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768852	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	54476
rs763978808	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5728322	CGGTGGCTCATGTAG[A/G]TAATCCCAGCACTGT	54476
rs763985728	snp	C/T	3.3961e-05	0.0041206	intron-variant	RNF216	GRCh38.p7	7:5730869	CAAATCCCACACCTG[C/T]CCATTGCTTCAAATG	54476
rs763995228	snp	C/T	1.73072e-05	0.00294165	intron-variant	RNF216	GRCh38.p7	7:5641123	TCTATTTTCTCCCTA[C/T]AAAGCAATAGGCAGC	54476
rs764002568	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5750263	GGCTCAGGAACCTCC[A/G]GATGCTGGATACAGC	54476
rs764013891	in-del	-/TTTTTTG			intron-variant	RNF216	GRCh38.p7	7:5715754	TTTTTTTTTTTTTTT[-/TTTTTTG]AGATGGAGTCTCACT	54476
rs764018618	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677841	CCAGTAGAATCAGGG[A/G]AAGGAGGATACTGGA	54476
rs764057916	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5695710	TCCCCTAGTCATCCT[C/T]GGATGGATGGTGCAC	54476
rs764064259	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5745725	ACCAACATGGTGAAA[-/C]CCCATCTCTACTAAA	54476
rs764067384	in-del	-/AAAAAAAAAAA			intron-variant	RNF216	GRCh38.p7	7:5738090	TAAGACTGTCTCCAA[-/AAAAAAAAAAA]AAAAAAAAAAAAAAA	54476
rs764071175	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5720885	TTATGACAAAATCCA[C/G]GTTTTTTCTTTTAAA	54476
rs764079518	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5626466	CCCCAACAAATTAAG[C/T]GAACTGATCCAGAAA	54476
rs764081820	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5774205	TCCCATTTAGTCAAT[C/T]GGTGGCTCCAGATAA	54476
rs764102068	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5634844	CCCTGCTTGGGAAAG[C/T]CCTCAGTGACATCGA	54476
rs764116009	snp	A/C/T			intron-variant	RNF216	GRCh38.p7	7:5770385	AGAATCACTTGAACC[A/C/T]GGGAGGCGGAGGTTG	54476
rs764117185	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5650406	GGCTGTGCTTTGTAA[G/T]TAATTCTCCTTCCAA	54476
rs764124358	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672561	TTCTGAGAATAAAAA[C/G]AGGTTTCCAGAATTC	54476
rs764138474	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667647	CTTTGCTCACTGCTT[A/G]GGCTACCTCTGGGCT	54476
rs764149790	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5696494	AGCAGCAACTGCCCA[A/G]TGATCTACTCCAGGG	54476
rs764156217	in-del	-/TTCT			intron-variant	RNF216	GRCh38.p7	7:5707211	CTTCCAGCTTTGTTC[-/TTCT]TTCTTAAGACTGTCT	54476
rs764188412	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5635928	ATTTGAACTGGACAG[A/G]TTTCAAACTCTTACA	54476
rs764196801	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5749332	ATTTTTGTATTTTTA[A/G]TAGAGACGAGGTTTC	54476
rs764223823	in-del	-/GAGTGCTTGTAGCCA			intron-variant	RNF216	GRCh38.p7	7:5769905	GCCAGGCTTGGTGGC[-/GAGTGCTTGTAGCCA]GAGTGCTTGTAGCCA	54476
rs764228194	snp	C/G	6.58903e-05	0.00573941	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741273	TTCCTGAGGAACGAC[C/G]TGGTTTGTTATTTCA	54476
rs764231631	in-del	-/TG			intron-variant	RNF216	GRCh38.p7	7:5779462	GGCAAAGCCAGGCCA[-/TG]TATTAGCCTTCTTCC	54476
rs764246508	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5729919	AGAGAGACAGTCAAA[C/G]AATCTATGGGGAGTT	54476
rs764258214	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5705801	AATCACAGCTACTCG[C/G]GAGGCTGGGGCAGGA	54476
rs764305385	in-del	-/TC			intron-variant	RNF216	GRCh38.p7	7:5650116	ATGAAGTTCTGGTGG[-/TC]TCTGGAGGTCAGGCA	54476
rs764306925	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681335	ACCTGTTTTAGGAAA[A/G]AATACAAACTTTATT	54476
rs764311704	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5748059	ACTGTTGCTAAGCTC[A/C]ATACCAATAGGCGGT	54476
rs764353980	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5779158	TTTGTAAACACATTA[A/T]ATAGTAGCTGGTAGT	54476
rs764355118	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5696565	GCCTCCTAGACACGC[A/G]TGCCCAAGATCGTGT	54476
rs764373872	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5723398	TCAAGCCTGTAATCT[C/T]GCACTTTGGGAGGCC	54476
rs764385138	snp	C/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753294	TTTAAAGTGAAATAA[C/T]GGTCTCCCAATCCAT	54476
rs764394430	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5752620	TGACAACAGTGGAAT[A/T]TGGTGCGTTAATAGT	54476
rs764410251	snp	A/G			synonymous-codon, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711814	CATCACTGTCCAACA[A/G]AGCCGGAAAGCTACA	54476
rs764416884	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5655853	CATATTACGAAGAAA[C/T]GCTCTTGAATGGTTT	54476
rs764419405	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5689686	GGCCAGGCATGGTGG[C/T]TCACGCCTGTAATCC	54476
rs764421731	in-del	-/A	0.000746803	0.0193092	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712888	GGCGAAAAGGCAAAG[-/A]AAAAAAAATCAATAC	54476
rs764426996	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5636244	AGAGCTGGCTTTCCA[C/G]TCTGCTCCCTAATCC	54476
rs764444596	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5744384	CGTCAAGAACAAAAA[A/G]GTCTTCAAAACACAT	54476
rs764452328	snp	C/G/T			intron-variant	RNF216	GRCh38.p7	7:5704972	CTCTCCACTGCAAAA[C/G/T]GTTGCTGAGGGGCAT	54476
rs764464402	snp	C/T	1.65067e-05	0.00287282	missense	RNF216	GRCh38.p7	7:5715159	AATGGAAATTCCCCA[C/T]AGCAGCAGCGACACT	54476
rs764471333	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5682771	GTGCAACACTTTTGG[A/G]AAGAAATTTGAAACT	54476
rs764478108	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5685430	GGGTGTAAGGGAGGA[C/T]TGTTGGGAGGGCAGG	54476
rs764505808	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5707063	GGTGTTCTTTGCACC[C/G]TTGTTGAAGATCAGC	54476
rs764507364	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5690718	CAGGGCTAGTGAGAG[G/T]TAGAGTGAAGATCTC	54476
rs764521549	snp	A/G	4.94776e-05	0.00497357	synonymous-codon	RNF216	GRCh38.p7	7:5715112	ACTCTTTGCAGAACA[A/G]GTGAGCATCTGCGCA	54476
rs764544730	snp	A/T	1.64741e-05	0.00286998	missense	RNF216	GRCh38.p7	7:5641270	GACAGAGGTAGCACA[A/T]CTGGGCACCACAGCG	54476
rs764550112	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5748458	AGAGACGGGGTTTCA[C/T]CATCTTGGCCAGACT	54476
rs764552138	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5735311	ATATGAGCTTAGAGT[C/G]AAATTTAGAAAATAC	54476
rs764558701	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5705580	CTGCACATCCCTCTT[C/G]GCAGAGGGAAAAAAT	54476
rs764570011	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5773972	CTAATTTAGTTGAAA[C/T]GTCAGGCTTGTAGTT	54476
rs764582620	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5735239	CACTGCCCTTGGGGA[C/T]TTGAAAGAAGCAAAA	54476
rs764599832	in-del	-/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668224	AATAGCAAAGCGGAC[-/T]TTTTTTTTTTTTTTT	54476
rs764612831	in-del	-/T	3.33667e-05	0.00408439	intron-variant	RNF216	GRCh38.p7	7:5725320	CCAACACAGTTTGCA[-/T]TACCTTGTTCAAACT	54476
rs764651811	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5708242	GAATATTTTGTATGT[A/G]TCTGTTAGGTCTATA	54476
rs764660364	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5649070	TGCTTGAAAACACTA[C/T]AGCAGTTTAAAAACA	54476
rs764673788	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5637891	TGTTCTGTTGTCCTG[A/G]GTGGAGTGCGGTGGC	54476
rs764678326	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672915	CTATCGTTTGACCAA[C/G]GGGGATGTCTTGAAA	54476
rs764691233	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5699866	TGTGACAGAGACCCT[C/G]TGTATTCTTTATCTT	54476
rs764694337	snp	C/G/T	3.75198e-05	0.00433114	intron-variant	RNF216	GRCh38.p7	7:5752825	CAATAATGTCTCATT[C/G/T]TAAGTTTAAAGAAAA	54476
rs764700304	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5763295	ACTCACTGAACTATA[C/T]ACTAAAATGGATGGA	54476
rs764713115	snp	C/G	1.64746e-05	0.00287002	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741114	ACTTGCTAACTGCTG[C/G]TCTTCAAACTCTCCT	54476
rs764748077	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5747356	ACCAGGGGAAGGAGA[A/G]GGAGTAAAAACGGAT	54476
rs764766061	snp	A/G	1.65214e-05	0.0028741	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741036	TTCTTGCCCCCAAAT[A/G]TTTTCCAAATTGGGC	54476
rs764781941	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5766608	TCCAACAATGCTGAA[A/G]CTCTATTCTCAGACT	54476
rs764783959	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5770679	AACCAAAGCATTCAT[A/G]GAGAAAAACAAAAGG	54476
rs764803497	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5703410	CAGCTGGAGCTGCCC[A/T]GGCATTGATAGCTGG	54476
rs764822098	snp	A/G	3.34549e-05	0.00408978	missense, intron-variant	RNF216	GRCh38.p7	7:5741796	ATGAGATTGGGTCGT[A/G]ATCTCTGAGGTTTAT	54476
rs764825312	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5757046	CATTATCATGTAATT[A/C]AAAATATCTTCTAAT	54476
rs764840198	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673852	CCTCCATCTCTCTCT[C/T]TCTCTCATTTTTTTT	54476
rs764843600	snp	A/G			upstream-variant-2KB	RNF216	GRCh38.p7	7:5783003	CCAGGAGTTTGAGAC[A/G]ATCCTGGGCAATAGA	54476
rs764867167	snp	A/G	8.24817e-05	0.00642137	intron-variant	RNF216	GRCh38.p7	7:5652550	GACAACTCCTGGTGA[A/G]TGGACACCACAGAAG	54476
rs764870634	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5685516	TACAACTTTGAAAAC[A/T]GCAAGCTACACGGTG	54476
rs764892505	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668536	CCACAAAGCGGACTT[C/T]TAATCTTTCCCTCCT	54476
rs764899729	in-del	-/AC			intron-variant	RNF216	GRCh38.p7	7:5731225	CATTTACAGTAAAAA[-/AC]AGTCTGCTAAGAGAT	54476
rs764902629	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5710985	AGAAATAAAGTTTTG[A/G]TCCATTAGTTTAGTT	54476
rs764908245	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674823	CAACATGGCAAAACC[C/T]CATCTCTACTAAAAA	54476
rs764920439	snp	C/T	1.6473e-05	0.00286988	missense	RNF216	GRCh38.p7	7:5652470	TCACAGGTGAGGCCA[C/T]TATGTTCTTTCCAGA	54476
rs764955187	snp	C/T			synonymous-codon	RNF216	GRCh38.p7	7:5622872	CCATCAGAAGCGATG[C/T]CGCGGCTGGGGGCCA	54476
rs764957867	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5730605	TCGGCTAGTCTTTAA[A/G]AACTTGTCCCAACAA	54476
rs764971477	snp	C/T	1.82477e-05	0.00302051	intron-variant	RNF216	GRCh38.p7	7:5730675	CAACAAAGCACAGCA[C/T]TTCCAGGCAGTGACT	54476
rs764976295	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5774321	ATGTGCCCAAGTCCC[A/C]GCTTTACTGTGGTTG	54476
rs765000989	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5702135	ATGCAGGTGGGTGTG[C/G]GCTCTGCCACCTGCC	54476
rs765019115	snp	A/T	1.73342e-05	0.00294394	missense	RNF216	GRCh38.p7	7:5624109	TGGATTTCCTCAATA[A/T]GCTTCTCATCATCTT	54476
rs765025959	snp	C/T	1.64743e-05	0.00287	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741350	AGTCTTCTTCGATGG[C/T]CTGATCATCTGCTAG	54476
rs765026679	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5722176	TGATCCACCAGCCTT[A/G]GCCTCCCAAAGTGCT	54476
rs765026868	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5729300	CAAATACCCATCTAT[C/T]TATCTTCACCCTAAT	54476
rs765031829	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5721570	ACCTGCGAATTGCTA[C/G]ATCATGGGATAGGCT	54476
rs765035148	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5717893	GCTCAAGAGATCCTC[C/T]CACCTCAGCTTCCCG	54476
rs765043348	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5623753	TGCTTTTCAGCCTCA[A/G]AAGGATCAGCTGGGT	54476
rs765057816	in-del	-/AGCCATTAA			intron-variant	RNF216	GRCh38.p7	7:5658243	TTTTCCAGCAATGAC[-/AGCCATTAA]AGCCAAGTATCTGAA	54476
rs765067813	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662727	CTACTCACAAACAGA[C/T]AACTGTATACTCTGA	54476
rs765069396	snp	C/T	1.91705e-05	0.00309595	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5730749	GCCAGCAGACTGCTA[C/T]TGGGATTTATAATGA	54476
rs765095183	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677974	CAGTAAGACCACAGT[C/G]ATCTTTCCAGGGGGT	54476
rs765100076	in-del	-/TTTTTTT			intron-variant	RNF216	GRCh38.p7	7:5715738	TCACCAACTCATTCT[-/TTTTTTT]TTTTTTTTTTTTTTT	54476
rs765100195	snp	C/G	1.65111e-05	0.0028732	intron-variant	RNF216	GRCh38.p7	7:5716698	GCCCAGAATAAACAA[C/G]GTGAGATTTCAAACT	54476
rs765122239	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669181	GGAATATGGGCGGTC[A/G]GGCTCCAGCTATACC	54476
rs765135550	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5760140	TTCGAATTTAACAGG[A/C]AATTTCACAAACATG	54476
rs765147542	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5633259	TGGGCTTACAGGTGT[C/G]AGCCACTGCGCCCAG	54476
rs765152327	snp	C/T			missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741011	CGAGCTCTTGATCTA[C/T]CTCTGCAGCTTCTTG	54476
rs765156428	snp	C/G	1.65798e-05	0.00287917	missense, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712783	ATAGTACTTATACAG[C/G]ATGGTCTGGGGGAGC	54476
rs765163007	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5632249	CTGCCACAGATCCAT[C/G]ACAGACCATGGTGCA	54476
rs765172420	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5775568	TCCCTTTGACTTCCC[A/G]GCAAAAAGTGGGCAA	54476
rs765190551	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5660498	GGTTTCACCATGTCG[A/G]CCAGGATGGTCTCCA	54476
rs765206046	snp	A/C			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712519	TTTTCCATTAATAGA[A/C]TTACTGGTTACTCAA	54476
rs765213596	snp	A/C	3.68623e-05	0.00429299	intron-variant	RNF216	GRCh38.p7	7:5623219	GAGAAAAACATTAAA[A/C]CAACCTCAATGGAAT	54476
rs765234979	in-del	-/A	1.73643e-05	0.0029465	intron-variant	RNF216	GRCh38.p7	7:5741821	GTTTATTTGTCTAAG[-/A]AAAAATGAAATTTTA	54476
rs765257136	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5732449	TAGATATGATTTCTT[A/G]AAAAAACAAAACATG	54476
rs765274032	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5688456	TGACACTAGTGAAAA[C/G]AAGAACACATACTGA	54476
rs765274792	snp	G/T	1.6593e-05	0.00288031	intron-variant	RNF216	GRCh38.p7	7:5721198	TACGACAATGCAAAA[G/T]CATGCAGACAACTAT	54476
rs765295498	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5650273	TTCTGCTCTTATCCA[C/T]TTACTGCTGATCTAA	54476
rs765306399	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5636997	GCTGAGAATAGGCCA[C/G]ACTGTTAACACCCAC	54476
rs765311484	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5719675	CATTCTATAACAGAT[A/G]GATCAAAACAATAAA	54476
rs765318126	snp	C/T	4.17275e-05	0.0045675	intron-variant	RNF216	GRCh38.p7	7:5739235	ACATATATTTTACCA[C/T]CACCACCACCACCAC	54476
rs765319052	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5776130	TCCATATCCATATGT[A/G]AAAGCTGTGGATATG	54476
rs765327870	snp	A/G	1.64738e-05	0.00286995	stop-gained	RNF216	GRCh38.p7	7:5721104	GAAGGAGAGCACGTC[A/G]GTCATAGGACCTACA	54476
rs765330061	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5759058	GATTTAGCACAATCC[A/G]TTCTGGTTGCAACAG	54476
rs765356095	snp	G/T	1.83024e-05	0.00302504	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622831	TACCCCAAACGGGCT[G/T]TGTGCTGCTCAATGG	54476
rs765390172	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5626874	GTAAATGCTCATGAT[A/T]AGGACACAGGAACAC	54476
rs765396065	snp	C/G			upstream-variant-2KB	RNF216	GRCh38.p7	7:5781873	ACCCCCATATCCGAC[C/G]CCACAAGGAGCCACC	54476
rs765400260	in-del	-/GAG			intron-variant	RNF216	GRCh38.p7	7:5637169	AGCTGCCAGGGGGCT[-/GAG]GAGGTGAGTCAGCAG	54476
rs765408314	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5651599	TGGTAAGGCTAGATT[A/G]TTATGAGAGAAGAGA	54476
rs765438150	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5770551	AAAGTTCAATTTTGC[A/G]AAGATGTCCTTTCAC	54476
rs765440685	snp	A/G	1.6473e-05	0.00286988	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741627	CAGAAATTCACCGTA[A/G]TCATCCTCAGAATCA	54476
rs765445210	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5766517	AGATCTAGAGAGCTT[A/G]CTTTTTCTCTCCATC	54476
rs765448062	snp	C/T	1.64735e-05	0.00286993	missense	RNF216	GRCh38.p7	7:5641246	GGTCATATCCATTAA[C/T]AGAAACTCGACAGAG	54476
rs765500938	snp	C/G	1.65141e-05	0.00287346	missense	RNF216	GRCh38.p7	7:5715087	GCCTCTTGGGCATAT[C/G]TGATGAGACACTCTT	54476
rs765513171	snp	G/T	3.29451e-05	0.00405851	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741540	TTGGTTATGACTCGG[G/T]CCAGGCTTGGGTTCT	54476
rs765520728	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5650149	TATATCATGATATCC[C/T]TTCCAAAGCTAGGCT	54476
rs765533943	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5774990	CCTCAGGTGATCCAC[A/C]CCCCCGACACTCACC	54476
rs765554557	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5646982	AGCCCTAGACATGTA[A/C]GTAGTCTTCTAGATC	54476
rs765596599	in-del	-/AAAAAAAAAAAAAAAAAAAAAAATAAAA			intron-variant	RNF216	GRCh38.p7	7:5653603	AGACTCTGTCTCAAA[-/AAAAAAAAAAAAAAAAAAAAAAATAAAA]AAAAAAAAAAAAAAA	54476
rs765607361	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5749323	GCCTGGTTAATTTTT[A/G]TATTTTTAGTAGAGA	54476
rs765615109	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5746431	AACTCCATTTGCTGC[C/T]AGCATACAGGGGTGC	54476
rs765615906	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5779420	CCCCACACCCCAGGC[A/G]CAATAAATTATGAAA	54476
rs765622909	snp	C/T	1.64732e-05	0.0028699	stop-gained	RNF216	GRCh38.p7	7:5729475	AGCTCGTGCAGGGCC[C/T]ACTTGATGTCCTGAC	54476
rs765644727	in-del	-/A			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780614	TGAGGCTGAGGCAGG[-/A]AAATCGCTTGAATCC	54476
rs765645547	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5687302	TTGGGAGGCTGAGGA[A/G]GGAGAATCACTTGAA	54476
rs765649698	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667995	GAGCAGGTAACTTCG[C/T]GTTGGTATTTTAGGG	54476
rs765655765	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5656883	AACCAGTAGACAAAT[A/G]TATCCGGCCACCACC	54476
rs765662032	snp	C/T	4.9879e-05	0.0049937	intron-variant	RNF216	GRCh38.p7	7:5641141	AGCAATAGGCAGCCA[C/T]GTGTCTACTTACAGT	54476
rs765678893	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5757591	TGATATATGCAACAA[A/C]AGGGATGAATCTCAA	54476
rs765697567	in-del	-/CA			intron-variant	RNF216	GRCh38.p7	7:5692624	AGTTCCAGCTCCTTC[-/CA]CACACACCACAAAAC	54476
rs765706397	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5631102	TTCTGAAACCTCCTT[C/T]CTCCCCTTACAAGAC	54476
rs765707116	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5777839	AAAAATTAAACTCAA[-/A]AATCTTCAGTGGGCG	54476
rs765715189	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5744490	GAGGGGGACACATAA[C/T]GGTTAGTTCAAATAA	54476
rs765736805	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5650338	GCTATGTGTGGCAGA[C/T]CAAGACGCTGAGCGG	54476
rs765747779	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5645977	CATGGTTTCACCTGG[C/G]TTTCTGAGCATATTT	54476
rs765768349	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5700830	CATGGGTGGGCAGGA[C/T]GACCAGTGCCCTCCC	54476
rs765773341	snp	A/G	3.29462e-05	0.00405857	missense	RNF216	GRCh38.p7	7:5652446	ATGTCGTCTTTTTCA[A/G]CCAGCTCTTCACAGG	54476
rs765778248	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5724804	GATAAAATCTGAGTT[C/G]TTATAACACTCAAGT	54476
rs765781602	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675952	GACCTCAGATGATCC[A/G]CCCACCTCAGCCTTC	54476
rs765785361	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666966	ACCACAGGCACATGC[C/T]ACCATACCTGGCTAA	54476
rs765791970	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5699918	ACTGAGGAATAAAAG[A/G]CCTTTTACGTTCTCA	54476
rs765794299	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5632135	CTGGACAGCGGTCTA[C/T]AGAGGTTCACCTGAA	54476
rs765799854	snp	A/C	3.60789e-05	0.00424714	intron-variant	RNF216	GRCh38.p7	7:5740967	ACTTGATAAAATAAA[A/C]CTTACCGTTTCTTTC	54476
rs765801250	snp	C/T	1.64798e-05	0.00287047	missense	RNF216	GRCh38.p7	7:5761062	TCATTGTTGTTTCCC[C/T]CTTCCATTTTCAAAT	54476
rs765810520	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5638967	ATAATTTTTTTAAAC[A/T]TCCTCTGTCCATTTT	54476
rs765811148	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669335	AAATGATGAGATCTT[C/T]AGAAGACCAATCTTT	54476
rs765826331	snp	C/T	1.65318e-05	0.002875	intron-variant	RNF216	GRCh38.p7	7:5716686	GCCCATGAAAATGCC[C/T]AGAATAAACAAGGTG	54476
rs765831946	snp	A/G			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620891	GTGATGTCTACAGCC[A/G]CCCTCTGCTCCCAGA	54476
rs765852102	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5656121	TAAAAATACAAAAAT[C/T]AGCCGGGCATGGTGG	54476
rs765869673	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665679	TTCGAGGACAGAGTG[A/G]GAGGGTAAAGTCTTT	54476
rs765890988	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5737717	TTGGCAGGGAAGAAA[C/G]TCACCTGCAACCTTG	54476
rs765924192	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5757192	TTTCAGTTACTGAAA[A/C]AAGTCTTAAAAATCC	54476
rs765930406	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5661657	AAAATACAAAAATTA[C/G]CCAGGCGTGGTGGTG	54476
rs765930668	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5749063	GACCTAACTCCAATG[C/T]CTTTTAGTTCACGTG	54476
rs765959122	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5772803	TTTTTTTGAGACAGA[A/G]TTTCGCTCTTGTCAT	54476
rs765974189	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5709623	TGTATATTCCTCCCA[C/T]AGACAAACAAAAACA	54476
rs765977902	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676779	CAGTGCAACCTGAGC[C/T]ACGACACAGAAAAGC	54476
rs765988212	snp	C/G	1.66217e-05	0.0028828	intron-variant	RNF216	GRCh38.p7	7:5715200	GCCATCCTGCAGGCA[C/G]TCAAGAAACACACAT	54476
rs765999708	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5773345	CCTCCTGGGTTCAAG[C/T]GATTCTTCTGCCTCA	54476
rs766004440	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5718894	GAACTCCTGGCCTCA[A/C]GTGATTGCCTGCCTT	54476
rs766018787	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5646547	AAATACAAAAAATTA[C/G]CTGGGTGTGGTGGCA	54476
rs766033008	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5634101	GCTTGGCACAAAACT[A/G]TTTTTGCCAAAGCCT	54476
rs766039655	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5649870	CAACTGGTATGCTGC[A/G]AATGATTTGGAAAAT	54476
rs766047213	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5691461	AGAGAGGTTTCAAGG[C/T]TAAAGGCAGTAATGG	54476
rs766051319	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5777197	CGGATGCTCCAGCAC[C/T]GGCCACCTCTGCTGA	54476
rs766054636	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5657969	TTGGTCCTTGCCCTC[A/G]AGGAGTGCACTCTAC	54476
rs766136201	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5693844	GACAGAGATGGACGC[A/G]GGTAGAGACTCTCTG	54476
rs766147457	in-del	-/TTT			intron-variant	RNF216	GRCh38.p7	7:5722382	ATGTTTTTTTTTTTG[-/TTT]GTTTGTTTGTTTTGT	54476
rs766165446	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5709141	GCAATGAGGAGTCAG[C/T]ACGTGCTAGTTTCAC	54476
rs766169049	in-del	-/A			intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652249	CATGAGGCTGCAGAG[-/A]TGAGGAAACAGAGGC	54476
rs766171325	snp	A/C/G	8.25212e-05	0.00642291	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712696	GTTGGCAGATGGCAC[A/C/G]CTCTGCCTGAGAACG	54476
rs766176203	snp	C/T			downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620035	GGCGGGGTGGAGAGA[C/T]GAAGCTGGAGGGAGC	54476
rs766181991	snp	A/G	1.66654e-05	0.00288659	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753012	ACACTGTTACTGGGA[A/G]GTTGGCACTATCACA	54476
rs766203671	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5729344	ATCATAAACCATCCC[A/G]ATTTCCACAAGCTGA	54476
rs766219257	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5766832	AAAAATGTTTAAAAG[G/T]TGAAACTAAAATTCT	54476
rs766222806	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5685000	GCAGTCTTTACACAG[A/C]ATAGGTGGAGGGGTG	54476
rs766225151	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5643235	CCTTTGCTTCTGCAT[A/T]TGTAAGAGTAGTACT	54476
rs766226194	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5756423	CGAGGCTAAAATATT[A/T]ACTACTTAGCTCTTC	54476
rs766255810	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5703663	TAAATACAAGTGACA[A/T]TGGGAAAAGATGGGT	54476
rs766258569	snp	G/T	1.66557e-05	0.00288575	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5729582	AGAATAGTCAAAAAA[G/T]TCTATTTTAGGCAAC	54476
rs766262398	snp	G/T	1.64743e-05	0.00287	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741348	GCAGTCTTCTTCGAT[G/T]GCCTGATCATCTGCT	54476
rs766273671	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5752097	GGCTGAGGCAGGAGA[A/G]TTGCTTGAAACCAGA	54476
rs766282621	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5777754	TAAATATGCAAACAA[G/T]TAGTCTAGAGTTTAA	54476
rs766290800	snp	C/T	3.34846e-05	0.0040916	synonymous-codon, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712825	CTCACTGGTTGGGAA[C/T]GAACACGTGCAGCTG	54476
rs766309670	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5623881	AAGGCGTTGAAGGCC[G/T]TTCCATAAGCCTGAG	54476
rs766315927	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5694204	TTTCCATTTTAGGAC[A/G]GCCTACTCAATTTCT	54476
rs766320743	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5763446	TACTAGCCGGGCCAA[C/T]GTGGTGAAACCCATT	54476
rs766348616	snp	C/T	1.65211e-05	0.00287407	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752932	GAATCCTTTCCTCAT[C/T]TGAGGAGTCAGATAT	54476
rs766365685	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5743342	CATACTGTTCTATAA[A/C]CTCTATCGAAAAAGG	54476
rs766367830	snp	A/T	3.46831e-05	0.00416417	intron-variant, nc-transcript-variant	RNF216, MIR6874	GRCh38.p7	7:5711901	TGATCTGGTTCCAGC[A/T]CCATGTGGCTGTTCA	54476
rs766371147	in-del	-/G			intron-variant	RNF216	GRCh38.p7	7:5656946	GAGACCTTTGGGTCT[-/G]GTTGGCAAAGAATCC	54476
rs766387238	in-del	-/AGAA	2.31206e-05	0.00339996	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712912	CAATACCATTTATAG[-/AGAA]AAAAATAAAAAGCGT	54476
rs766402362	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664585	TGTGCCCAAGAGAAC[C/T]TCTGGTTTAGAGGGG	54476
rs766404300	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5652867	ACAAGGAAAAATTTC[G/T]CTCCCTAGATCAAAA	54476
rs766422005	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669263	GTTGAGAAGCTCTGA[C/T]CTCTTTTGATCCAGG	54476
rs766430843	snp	G/T	0.000428705	0.0146345	intron-variant	RNF216	GRCh38.p7	7:5739229	TTTATTACATATATT[G/T]TACCACCACCACCAC	54476
rs766440219	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5627657	GAGGCTGAGGCAGGA[A/G]AATGGCTTGAACCTG	54476
rs766446986	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5688588	AAAAAAGTTAAAGGC[A/G]CATGTATTTACCAGC	54476
rs766449344	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5701937	TGACTGGTCTCCTGA[A/G]AAGGTGGAAACACTA	54476
rs766471256	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5751235	CCAGAACCTATAAAG[C/T]ATATGCTGGGACCAG	54476
rs766475427	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5635362	ACGCCAAAGCCAGCT[A/G]TGGAAGCTGGGTGAT	54476
rs766475558	snp	C/G			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712183	CAAGATATGTAGACA[C/G]AAGTTTGAGCTACAG	54476
rs766481206	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5627173	TCCCTGAGAAAGTAC[C/G]TTGTTCAATGTTACG	54476
rs766484579	snp	C/T			intron-variant, downstream-variant-500B	RNF216, RNF216-IT1	GRCh38.p7	7:5662186	TGGGATGGAATCAGA[C/T]CTGAGGATACCCTTT	54476
rs766488878	snp	C/T	2.12326e-05	0.00325819	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5730774	TAATGATTCTGTCTT[C/T]TCTCTTTGGATAATC	54476
rs766492677	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5653944	CCTGCACGCACCAGA[C/T]CAGGCAAGGCCTTGA	54476
rs766509613	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5749152	AAATGCCCATGTATT[-/T]TTTTTTTTTTTTTTT	54476
rs766532719	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5642401	GTATTTTTAGTAGAA[A/G]TGGGGTTTCACCATG	54476
rs766535534	in-del	-/TC			intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739619	AACAAATATTGAGCA[-/TC]TCTGTCTAGACAAAG	54476
rs766542329	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5636600	CACTGAACTTCTGAA[-/T]GGCTTTGTGTTCTCA	54476
rs766547016	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5701755	CACGCATTTCACTGC[-/T]CATTCATGGCCTCAC	54476
rs766552410	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682034	GCCACTTCTGTGGCC[A/G]GCTGCTGCCTCTTCT	54476
rs766561744	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5722339	TAATACATTTTATTT[C/T]GATTCTCCTTTTCTC	54476
rs766572535	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5775794	GAAATGCTTGAACCC[A/G]GGATGCAAAGCTTGC	54476
rs766621214	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679071	AGAGATTAGATACAG[C/T]GGAATGAATAACAGC	54476
rs766626232	snp	G/T	1.6525e-05	0.00287441	intron-variant	RNF216	GRCh38.p7	7:5729381	CATTCTGTTACCATG[G/T]GAAGATGTAGTCAAG	54476
rs766628122	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5683347	ACCCAGGCTGGAGTG[C/T]AGTGGTACAATCCAC	54476
rs766634468	in-del	-/AG			intron-variant	RNF216	GRCh38.p7	7:5761445	CAAAAAAGAAAACAC[-/AG]AAGATGCTCAACCTC	54476
rs766670267	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5733828	ACAAAAAATAACATC[A/G]TAACTCAGTATTGTC	54476
rs766671168	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5746518	GCTTTTGGAATCTGT[A/G]GGTATGTGGATTCCT	54476
rs766674430	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5637788	TCAAGAGATCTGCCC[A/G]CCTTGGGCTCTCGAA	54476
rs766687139	snp	A/C			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780758	AACGTTCTCTTTGCA[A/C]GATCTAAGTACCTAG	54476
rs766713741	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5707104	TGTGTGGATTTATTT[A/C]TGAGCACTGTATTAT	54476
rs766716300	snp	G/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673539	TCACGTGGGGCAGTA[G/T]GCAGGGAAGAGAGCA	54476
rs766746548	snp	C/G	1.6492e-05	0.00287154	synonymous-codon	RNF216	GRCh38.p7	7:5622965	CACGTTGGGCAGAGG[C/G]GGCACGTACGGGGCT	54476
rs766772595	snp	G/T	3.67728e-05	0.00428778	intron-variant	RNF216	GRCh38.p7	7:5624142	TAAAACGCAAGCAAT[G/T]AGAAGGATGAACCTG	54476
rs766818704	in-del	-/TG			intron-variant	RNF216	GRCh38.p7	7:5643535	ACTCCTGTAGTTATC[-/TG]TGCTCACCACCAGCC	54476
rs766822024	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5715659	GAAGCTATAACTAAA[G/T]CAGCAACCTCAAGTA	54476
rs766837334	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5689097	AATGATATCCTATTA[C/T]ATGGCACCACCATCA	54476
rs766854607	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5700099	CGCCCTGACACAGAC[A/C]CCCACGGGGACAGGG	54476
rs766859830	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5726578	TGTGTTCAAATCAGG[A/G]TGGGCGCGGTGGCTC	54476
rs766862574	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5754981	TGCAGTAAGCCAAGA[C/T]CATGCCACTGCACTC	54476
rs766879177	snp	C/T			upstream-variant-2KB	RNF216	GRCh38.p7	7:5782447	TGCTCCTGCTGGGCA[C/T]AGTGGCTCATGTCCA	54476
rs766892426	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5657616	TATAAATCTCCAGCA[C/T]TCTTGAGGTAAAAGG	54476
rs766913396	snp	C/T	1.6566e-05	0.00287797	missense	RNF216	GRCh38.p7	7:5715186	CACTCAATCAGCTGG[C/T]CATCCTGCAGGCAGT	54476
rs766937619	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682286	TCACCTCAGAGGCTA[C/T]TTGACCAGGTTACCC	54476
rs766940588	snp	A/G	1.65444e-05	0.00287609	missense	RNF216	GRCh38.p7	7:5622916	GGTTGTGCTCCAGGG[A/G]CATGTGGATGGGACC	54476
rs766944412	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5639983	CCAGGATGGTCTCGA[C/T]CTCCTGACCTTGTGA	54476
rs766951280	snp	C/T			upstream-variant-2KB	RNF216	GRCh38.p7	7:5782763	GCCGAGGCACAAGAA[C/T]TGCTTGAACCGAGGA	54476
rs766952965	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5631360	GGGAGTGGGGAGCTT[A/G]GGAAAGCTCATAACC	54476
rs766963004	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677808	ATGCAGAGACCATTA[C/G]AGTAACTAAATCAGA	54476
rs766963914	snp	C/T	1.64953e-05	0.00287182	intron-variant	RNF216	GRCh38.p7	7:5652543	ACACAAAGACAACTC[C/T]TGGTGAGTGGACACC	54476
rs766974543	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5656937	TAATAATCTTGAGAC[C/T]TTTGGGTCTGTTGGC	54476
rs766980488	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5745627	AACAAGGGCAGGGCA[C/T]GGTGGCTCACGCCTG	54476
rs766983712	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5646110	TTGCTTTATAAATTA[C/T]TGTTGAAAACTGGGT	54476
rs767014523	in-del	-/AAAC			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675640	AGCAAGACCCTCTCA[-/AAAC]AAACAAACAAACAAA	54476
rs767022604	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5653143	AAGGGAGACTTTCCT[A/C]CGTTGCTCATCACTC	54476
rs767047048	snp	A/T	1.64914e-05	0.00287149	missense	RNF216	GRCh38.p7	7:5715120	CAGAACAAGTGAGCA[A/T]CTGCGCACTGCGTCA	54476
rs767058307	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5740580	TTATTTAACTGTAAG[A/G]CATTTAAATGTAAAC	54476
rs767092585	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667991	AGCTGAGCAGGTAAC[C/T]TCGCGTTGGTATTTT	54476
rs767100420	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5773654	CTCACTGCAACCTCC[A/G]TCTCCCAGGTTCAAG	54476
rs767111076	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5658092	ATGCAGAGGAGAAAG[A/C]GGTGAGTCAGACAAG	54476
rs767117755	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5710816	CCTCCCCAGGCAGTC[C/T]AACACCTGACCCACT	54476
rs767125004	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5701549	TTTTGCACAAAAGCT[C/G]TACGAGGTAGGTGCA	54476
rs767134350	snp	C/G			intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739474	AAGGGCTGTGAAGCA[C/G]GTCTGTGTGTGTCTT	54476
rs767143684	snp	A/G	1.64727e-05	0.00286986	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5729518	TGAAGTCGGCCATGA[A/G]GAGGTCAGCAGCTTG	54476
rs767151828	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5709772	AAATTTTTTTCTTTT[A/G]AAGACAGAGTCTTAG	54476
rs767179508	snp	C/T			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620174	AAAGAAAAAGTTTAA[C/T]GAACTAATCGTTTCT	54476
rs767195404	snp	A/C/T	3.30225e-05	0.0040633	missense	RNF216	GRCh38.p7	7:5623054	GGAAGGGTGGGTGCG[A/C/T]GAAGGCATAGGGTGG	54476
rs767238439	snp	A/C	1.72844e-05	0.00293971	missense, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711803	GAACCTCTTCACATC[A/C]CTGTCCAACAGAGCC	54476
rs767267326	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5685655	TAAAACACCAGAAGC[C/T]AACCTGACATCAGTC	54476
rs767303715	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5704719	TAAACTCTCCTTTCT[C/T]ATCCAAAGGACAAGG	54476
rs767311334	snp	C/G	5.28849e-05	0.00514195	intron-variant, nc-transcript-variant	RNF216, MIR6874	GRCh38.p7	7:5711884	CTTCAAACATTAAAG[C/G]CTGATCTGGTTCCAG	54476
rs767321399	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5700998	CTGAATGTCATCCCT[A/G]AGATTCTAAACCTTC	54476
rs767322553	snp	C/T	1.65422e-05	0.0028759	intron-variant	RNF216	GRCh38.p7	7:5721183	GTCACCTAGAAGATA[C/T]ACGACAATGCAAAAG	54476
rs767323601	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5695650	GAGATGACAGAATGG[A/T]AAGTTGTCATTTGTT	54476
rs767344819	snp	C/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5768104	TTAAACCACAATGGA[C/G]GAGTATCATTTGGAA	54476
rs767349292	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5648552	AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT	54476
rs767355627	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5686396	GCTGGGACAGAAAAC[A/G]GGATCCCCATTTCTC	54476
rs767374065	snp	C/T	1.64727e-05	0.00286986	synonymous-codon	RNF216	GRCh38.p7	7:5721087	CTCTTGTTGCACAGC[C/T]GGAAGGAGAGCACGT	54476
rs767378243	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5661710	TGGGAGGCTGAGGCA[G/T]GAGAATCGTTCGAAC	54476
rs767389466	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5694867	ACTACTCCTGTTTTG[A/G]TTTTGAACATTTATT	54476
rs767393418	in-del	-/CA			intron-variant	RNF216	GRCh38.p7	7:5627787	CCCCCTTTTTTCCCT[-/CA]GACTCTCCCCTGATA	54476
rs767404334	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5744184	AGAAGAAGAATCGAA[C/T]GCAAATTCCAGAATG	54476
rs767411351	snp	A/G	1.66225e-05	0.00288287	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5752999	AGGAAAGCAGAGAAC[A/G]CTGTTACTGGGAGGT	54476
rs767419458	snp	A/T	1.6473e-05	0.00286988	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741192	CTGGGGTTCCGGCCT[A/T]GGAAAAGCGGGCCCT	54476
rs767437373	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5726194	AGATAGGACAATCAC[C/T]TGAGCCTGAGAGGCA	54476
rs767446065	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5758023	AATTAATGCAGCTAA[C/T]AAAAACAAAACTCTA	54476
rs767446130	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5748615	TTTTATATACATACA[C/T]ACACACACACACACA	54476
rs767464473	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5650345	GTGGCAGACCAAGAC[A/G]CTGAGCGGAACCAGT	54476
rs767466211	snp	C/T	0.000148944	0.00862842	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752914	CTGGGGTGACCAGCA[C/T]TGGAATCCTTTCCTC	54476
rs767492406	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5729870	CCATACCATATTTAC[A/G]AACAACTATTTTTTT	54476
rs767500481	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5635654	TGCGCTGGCCTGAGG[A/G]GAGAAGGCAGGCCTG	54476
rs767510241	snp	G/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753205	TCTAACAATTACTAT[G/T]CTCAAGATTATCAAC	54476
rs767519529	snp	C/T	1.71328e-05	0.00292679	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752860	CTTCTGTCAGGATGA[C/T]ATCATCATCCAGGTC	54476
rs767569201	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5655705	AGGCTGGGGAGTTTA[A/G]CATTTGGAGCTCTCT	54476
rs767571384	snp	A/G	1.65184e-05	0.00287384	synonymous-codon, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712729	CCTGACAAGCTCGTC[A/G]GCGTAGGCTGCCGCA	54476
rs767572883	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5660502	TCACCATGTCGGCCA[A/G]GATGGTCTCCATCTC	54476
rs767580975	in-del	-/CAAGA			intron-variant	RNF216	GRCh38.p7	7:5644334	TTTCTATATCTCTGT[-/CAAGA]CTTGTTATTTTCCAT	54476
rs767582435	snp	A/G	1.6473e-05	0.00286988	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741415	GTCTCTGAGTCTTCG[A/G]ATGACTGGTTCTGAG	54476
rs767598541	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5743639	TCATTTCTAAAAGTA[C/T]GTATATGTACCCACA	54476
rs767612061	snp	C/T	1.79664e-05	0.00299714	intron-variant	RNF216	GRCh38.p7	7:5624132	ATCATCTTCCTAAAA[C/T]GCAAGCAATGAGAAG	54476
rs767616045	in-del	-/GGCGA			utr-variant-5-prime, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781663	TTCCGGCCCTGCCGC[-/GGCGA]GGCGTCACCTCGCGC	54476
rs767631495	snp	C/T	1.6477e-05	0.00287024	missense	RNF216	GRCh38.p7	7:5761029	TGGCAGTGAAAGTTG[C/T]TCAAGTGAATTACCT	54476
rs767659116	snp	C/G	1.66117e-05	0.00288194	synonymous-codon, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712795	CAGGATGGTCTGGGG[C/G]AGCACCTTCTCCAGC	54476
rs767659193	in-del	-/ACAC			intron-variant	RNF216	GRCh38.p7	7:5748624	CATACACACACACAC[-/ACAC]ACACACACACACACA	54476
rs767660066	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5699695	AGAGATGGCAGGGAC[C/T]GCTGCCTTAGCCTGT	54476
rs767684610	snp	C/G	1.64776e-05	0.00287028	intron-variant	RNF216	GRCh38.p7	7:5760986	GGAAAGGGATGAAGT[C/G]AGAACAAACAACTTA	54476
rs767701300	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5714070	TGCAGTGGTGCGATC[A/T]CAGCTCACTAAGCCT	54476
rs767711218	in-del	-/TAAAAACAGGAGGGAGAAGGGGTACCTGAT			intron-variant	RNF216	GRCh38.p7	7:5726896	AAGTCTTTGCCATCC[lengthTooLong]TTGAAACGGAAGGAA	54476
rs767750053	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5689258	TGATATGGCAGCATT[C/T]TGGCTAGTTTGTGAG	54476
rs767769418	snp	A/C/G			intron-variant	RNF216	GRCh38.p7	7:5763659	CACTACAGCCTTGAA[A/C/G]CCCTGGGCTCAAGCA	54476
rs767786116	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5735220	TAAAGTCGTTTCAAA[A/C]TGACACTGCCCTTGG	54476
rs767799044	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712616	AAATGTCAAAAAACC[C/T]GGAAGATAAACACAA	54476
rs767806716	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5760477	GTCGAGATTACGCCA[C/T]TGCACTCTGGCCTGG	54476
rs767829520	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5777848	AACTCAAAATCTTCA[C/G]TGGGCGGGCTAAACA	54476
rs767858695	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5698062	TTCTGACGGGAAATA[A/C]AACTGAAAAAAAAGT	54476
rs767861847	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5637861	ACGCATTTCTTTTTC[C/T]TTAAGATCAAGTCTT	54476
rs767872366	in-del	-/TTC			intron-variant	RNF216	GRCh38.p7	7:5759627	TTGGTGGAGTCATTT[-/TTC]TTCTTCTTTTTTTTT	54476
rs767873301	snp	A/C/T	3.61332e-05	0.00425036	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622852	TGCTCAATGGGGATT[A/C/T]GGGGCCATCAGAAGC	54476
rs767886189	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5702315	CTTCTACCATTAGCA[C/T]CTGACATGAGGGATA	54476
rs767902226	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5723350	TCAGTCCTTTATTTT[A/G]AAAAATAAATGCAAT	54476
rs767902357	snp	G/T			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713259	GGGCAGGGACTCAAA[G/T]TAATAAACTGAAAAC	54476
rs767915764	snp	C/T	6.58924e-05	0.0057395	synonymous-codon, intron-variant	RNF216	GRCh38.p7	7:5741663	TGCCCCAGAATCAAA[C/T]AATGGGTTGTTACAC	54476
rs767920066	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5706938	CATTTAAAGAGTTGA[-/T]TTTTGTGTTATGATA	54476
rs767981806	snp	C/G	3.3534e-05	0.00409461	intron-variant	RNF216	GRCh38.p7	7:5725313	ACTGCCACCAACACA[C/G]TTTGCATTACCTTGT	54476
rs767987468	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5755938	CTTCACGTCCTTATG[A/G]GAACACAATCATGCT	54476
rs768021221	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5717821	AGAGTCTCACTTTGT[C/T]GCCCAGGCTGGAGTG	54476
rs768026192	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5770534	CCATATTCACGGGTG[C/G]GAAAGTTCAATTTTG	54476
rs768034068	snp	A/G	0.00104026	0.0227826	intron-variant	RNF216	GRCh38.p7	7:5760457	GGAGGCGGAGCTCGT[A/G]GTGAGTCGAGATTAC	54476
rs768052902	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5708179	CCATCCTGGAAAATG[C/T]TCCATGCGCAACAGA	54476
rs768060419	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5732161	AGAGTACATTTTCCT[A/T]TAAAACCATTGTCAT	54476
rs768079365	snp	C/T	1.8054e-05	0.00300444	intron-variant	RNF216	GRCh38.p7	7:5641396	AATAAGAAAACATAA[C/T]TTGGAGCTGGGAGGG	54476
rs768106266	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712346	AATGTGGTGGTGCAC[A/G]CCTGTAATCCAGGCT	54476
rs768126169	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5778174	ATCACCTGACCTTGC[C/T]GACATAGCGGGCCTT	54476
rs768135535	snp	C/T	1.65586e-05	0.00287733	intron-variant	RNF216	GRCh38.p7	7:5716669	CATGGTAAGAGAAAA[C/T]AGCCCATGAAAATGC	54476
rs768139919	in-del	-/TGGGAAATACAGCCAGACTCCGCCTCAAAAAAAAAA			intron-variant	RNF216	GRCh38.p7	7:5779803	CACTGCACTTTAGCC[lengthTooLong]AAAAAATGCTCAATG	54476
rs768141455	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673705	ACACAGCATGACCTT[C/G]TCTCTACAAAAAAAT	54476
rs768172393	snp	G/T	1.65116e-05	0.00287324	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712676	AGTTTTCACAATGGG[G/T]AAGAGTTGGCAGATG	54476
rs768174774	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679914	AGGCGGCTCCACAGT[C/T]GGCTTTAAGAAACAC	54476
rs768192435	snp	C/G			upstream-variant-2KB	RNF216	GRCh38.p7	7:5783592	CGGCAATGAGTGTTC[C/G]TTCTCTAAGACAGTA	54476
rs768192772	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5703036	TGAAGCTCTTCAGAG[A/G]GACCCATGCTGGGCT	54476
rs768194565	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5772125	GTAATCCCAGCTACT[C/G]AGGACGCTGAGGCAG	54476
rs768199027	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5653998	TTTATCCTATGAGCA[C/T]TAGGAAGCCCCCAAA	54476
rs768207780	snp	A/C			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678745	CTGTGAGAGCTACAG[A/C]AGTGGGACAAGCTGC	54476
rs768214991	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664714	CACGCTTCCCCCACT[A/G]GCCAGCATTCTCCTC	54476
rs768223808	snp	A/G	1.72668e-05	0.00293822	intron-variant	RNF216	GRCh38.p7	7:5725285	AAGAAAAGGTACAGT[A/G]TTGCAGCTACACACT	54476
rs768243299	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5721991	GCAGTGGCACATTCA[C/G]AGATCACTGCAGCCT	54476
rs768249100	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5628936	TGCAGTTGGCTCATG[C/T]CTGTAATCCCAGCAC	54476
rs768260196	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5633599	AAAACAAAACAAAAC[-/A]AAAACAAGGAAATAA	54476
rs768262823	snp	C/T	1.651e-05	0.0028731	missense	RNF216	GRCh38.p7	7:5721170	TTTCTATTTTTATGT[C/T]ACCTAGAAGATATAC	54476
rs768267749	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5713980	TGACTCCAAAGGTCA[C/T]GCTCTTTGAAAAAAC	54476
rs768278816	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5693584	GCCAAGCTTAAAGAG[C/G]GAACTTCAGAGCAAG	54476
rs768316289	snp	A/C	1.71472e-05	0.00292802	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739323	TATTTCCTCAATAAA[A/C]CCATTTGCTACATCT	54476
rs768331192	snp	C/G			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712684	CAATGGGGAAGAGTT[C/G]GCAGATGGCACGCTC	54476
rs768331795	snp	G/T			missense	RNF216	GRCh38.p7	7:5652439	GTACTTGATGTCGTC[G/T]TTTTCAGCCAGCTCT	54476
rs768339115	snp	C/G			downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619868	TGCCTAGCAGATCAC[C/G]TGATCTTCCTCCCTG	54476
rs768355146	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5760092	TACACCTCAGCATGA[C/T]TTTTTTCCTTTTAGC	54476
rs768359156	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664206	ATCTCCTCTCTGAAA[A/G]AACATTATTTCCTCC	54476
rs768361536	snp	A/C	0.000134309	0.00819369	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739525	AGATTCATCTGTCTA[A/C]ATAGAAGATGAGGTC	54476
rs768376912	in-del	-/TT			intron-variant	RNF216	GRCh38.p7	7:5776699	CGTGTCAGATCTGGG[-/TT]TTTATCCTTTAAAAG	54476
rs768392777	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5653695	CCTAATAGGTTACAG[C/T]GAAGGAAAACATAGT	54476
rs768404052	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5688321	AGACTCACATATCTG[C/G]AAATCATAAACAAGG	54476
rs768417988	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5777247	AAATGGCCCAGGTGA[C/G]CACTTCTCAATTCTC	54476
rs768439302	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5653831	GAAAACAGATCAACA[C/T]TCCAGACAATGGGCA	54476
rs768442220	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5701439	TCTCCTGAGGCCGCA[C/T]ATCTGCACACACCAT	54476
rs768444972	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5703726	CACGAAAAGACTACA[C/T]CAGATGTTCTTCAGT	54476
rs768457698	snp	C/G			upstream-variant-2KB	RNF216	GRCh38.p7	7:5782396	GCCTCAGGAAGTTTA[C/G]GTTTTAGTGAGCAAG	54476
rs768467399	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5752459	TTATATATATATCTT[C/T]ATATTTTGGAACTAA	54476
rs768474255	snp	A/T	1.64727e-05	0.00286986	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741618	CCCAAGATCCAGAAA[A/T]TCACCGTAGTCATCC	54476
rs768479669	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5685864	AAAACATTTTCAGTA[-/T]TGTGAATTCTTTATA	54476
rs768480634	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5642806	CTAATGAAAAACTTT[G/T]CAATTTGAAAAGCTA	54476
rs768525706	snp	C/G	4.94173e-05	0.00497053	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741520	TTGACAATGTCATTT[C/G]CTGCTTGGTTATGAC	54476
rs768550427	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5636923	CAATCCCAGGCATGG[A/G]AAGCAACGGGAGGAG	54476
rs768559210	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5688803	AGTTTATTTAGCTTT[C/T]TTATTAGTGAAAGAG	54476
rs768560483	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5772669	CATTTTCTCAACTTA[C/T]AGAATGTGAAGTTAT	54476
rs768594731	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5652588	TCAACAAAAGGGATA[C/T]GAAATGAGCTTTACT	54476
rs768595073	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5634736	CATGTTTTGCGTCCC[A/G]TCAGGGTCAAGTGCT	54476
rs768596220	snp	C/T	1.64811e-05	0.00287059	missense	RNF216	GRCh38.p7	7:5725380	TGTTTTCTCTTCTTC[C/T]TTTTTCCACTGGTTT	54476
rs768602199	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5716341	ATGGTGAAACCCCGT[C/G]TCTACTAAAAATACA	54476
rs768608039	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5648176	CAATGGCGTGATCTC[A/G]GCTCACCATAACCTC	54476
rs768619299	snp	C/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767794	AGTAAAGAGGAGACT[C/T]TGTTATGTTGGCCAG	54476
rs768627197	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5698683	ATAGGCATGAGCCAC[C/T]GCTCCGGCCTCTTGG	54476
rs768628514	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673336	GTTCAAGAACAGGCT[C/T]GACAGAATGGAGTGG	54476
rs768632728	snp	A/G			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622436	ATGCTTCCCAGGCCC[A/G]CAGGTGCAGCCCCCT	54476
rs768643138	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5775687	CCAGCCTGGCCAACA[A/C]GGTAAAACCTGTCTC	54476
rs768650322	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5771868	ACGGCTGAGTACCCC[A/G]AGGAAACGCAAAAGG	54476
rs768669730	in-del	-/GACA			intron-variant	RNF216	GRCh38.p7	7:5730256	AAAGTTGTGCTGATG[-/GACA]GACAGAGGACATATG	54476
rs768674925	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682119	GCACCTGAGGCCATG[C/T]GGGCCCACGCTGCTA	54476
rs768679037	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5692279	CCTTTTACTTGTTCC[G/T]CACATACCAAAAGCT	54476
rs768685479	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5733299	GTTTAAGGATCAGTG[G/T]TTGTTTCTGAGTGAC	54476
rs768696130	in-del	-/AAAATAAAT			intron-variant	RNF216	GRCh38.p7	7:5723654	CCGTCTCAAAAAAAA[-/AAAATAAAT]AAAATAAATAAATAA	54476
rs768697658	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5637639	GCATCCCTAACGTCC[C/T]GGGCTAAAGCAATCG	54476
rs768766656	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5682983	AACCAACATAAATCT[C/G]TGTGATGGAATGACA	54476
rs768771413	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5727112	TCCCAGTCTGGGCAG[C/G]AATGAGAAGCGGGGT	54476
rs768772383	snp	A/G	1.71237e-05	0.00292602	intron-variant	RNF216	GRCh38.p7	7:5715022	CCAGGAATGTGTCCT[A/G]TATACATGGGACATA	54476
rs768779035	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5759038	GGGGGTGGTATTTCA[A/T]AAATGATTTAGCACA	54476
rs768788836	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5657419	CTAAAAATACAAAAT[G/T]AGCTGGGCGTGGTGG	54476
rs768792607	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670211	AGTGCTGGAATTACA[A/G]GCGTGAGCTACCGTG	54476
rs768796555	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5725753	TACTCAGGAGGCTGC[A/G]GCAGGAGAATCGCTT	54476
rs768848367	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5740412	ATTACAGGTGTGAGC[A/C]AGCACGCCCAGCCCT	54476
rs768870480	snp	C/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754691	TCCTCTCTTGAAGAA[C/T]TGACCCAAGAAAAAG	54476
rs768876902	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5657975	CTTGCCCTCAAGGAG[A/T]GCACTCTACTGAGAG	54476
rs768877358	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5691374	CCTGTTCTGGCTGGA[G/T]TGCTCCTGGCTGGAT	54476
rs768885067	snp	A/T	1.76316e-05	0.00296909	intron-variant	RNF216	GRCh38.p7	7:5741829	GTCTAAGAAAAAATG[A/T]AATTTTAATAATTCA	54476
rs768905450	in-del	-/AACA	3.29549e-05	0.00405911	intron-variant	RNF216	GRCh38.p7	7:5760989	AAGGGATGAAGTGAG[-/AACA]AACAACTTACCTTGT	54476
rs768911038	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5748556	TTCTTTATGATTTTC[C/T]TAACCTTTCCTCAGC	54476
rs768922237	snp	C/T	1.64841e-05	0.00287085	synonymous-codon	RNF216	GRCh38.p7	7:5716752	CATCTGTAGGGCAAG[C/T]AAAAAGTCTTCATGC	54476
rs768940013	snp	A/G	1.65647e-05	0.00287786	missense, intron-variant	RNF216	GRCh38.p7	7:5741775	TGCCACTGGGCAGCT[A/G]GTTTGATGAGATTGG	54476
rs768979510	snp	A/C	5.0352e-05	0.00501732	intron-variant	RNF216	GRCh38.p7	7:5715229	ATGAAATGTCCTGCA[A/C]TTAAGGAGAGGGGGA	54476
rs768981922	snp	C/G	1.64811e-05	0.00287059	intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652395	CAGCCCATAGCCCCT[C/G]TGAATTCTGTTACTC	54476
rs768993337	in-del	-/ATAAA	1.82871e-05	0.00302377	intron-variant	RNF216	GRCh38.p7	7:5740957	GTCTACATTTACTTG[-/ATAAA]ATAAAACTTACCGTT	54476
rs769009836	snp	C/T	0.000137466	0.00828941	intron-variant	RNF216	GRCh38.p7	7:5739227	TTTTTATTACATATA[C/T]TTTACCACCACCACC	54476
rs769029031	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5686882	CACAACAGGGTTCAC[A/G]CTCCTGAGACTCTAA	54476
rs769034499	snp	A/G	3.56462e-05	0.00422159	intron-variant	RNF216	GRCh38.p7	7:5729632	AAAATCAGAGGCCAG[A/G]CAGTACATTTCCCAT	54476
rs769040988	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5640674	TACGTTAATAGAATT[A/G]TTAATATTAAACCAT	54476
rs769060350	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5686149	AATCGCTTGAATCCA[C/G]AAGGCAGAGGTTGCA	54476
rs769070328	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5639594	GTCTCCTGAGTAGCT[G/T]GTATTACAGGCATCC	54476
rs769071178	in-del	-/AAA			intron-variant	RNF216	GRCh38.p7	7:5737547	AATAATAATAATAAT[-/AAA]TAAATAAATATAAAT	54476
rs769089631	snp	G/T	1.64985e-05	0.0028721	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5729565	TCAAGAGGGGTCAAT[G/T]TAGAATAGTCAAAAA	54476
rs769105436	snp	A/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676730	TGGCATTTCCGGCCT[A/T]ACAACTGGGAGAGAA	54476
rs769131095	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5701438	ATCTCCTGAGGCCGC[A/G]CATCTGCACACACCA	54476
rs769137105	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5773759	TTTTAGTAGAGAAGT[C/G]GTTTTGTCATGTTGG	54476
rs769146861	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5650239	GATTTTTGGAATCAA[C/T]ATATATCACATTTGG	54476
rs769175702	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5659168	AGGCGAGTTTAGTTC[C/T]AGACCAGCTTACTTA	54476
rs769190921	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5714336	CGATCTCAACTCACC[A/G]CAACCTCTGCCTCCC	54476
rs769238486	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5625315	ATATCGTGAGAGGAT[C/T]AGCAAGTCCCAACAA	54476
rs769241830	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666392	TGCGAAGGTGCATGT[A/G]AGTGAAGACTTAAGA	54476
rs769259546	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5705204	GATTTATGGAGCACC[C/T]ACTATGTGCCAGGCA	54476
rs769261218	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5708770	CTCAGCAGCTCCAAG[G/T]CATCTAGAGTAGGTT	54476
rs769264483	snp	C/T	3.55549e-05	0.00421618	intron-variant	RNF216	GRCh38.p7	7:5730847	GATGTTACTTTCATA[C/T]TGCTTCCAAATCCCA	54476
rs769275094	snp	G/T	5.83096e-05	0.0053992	intron-variant	RNF216	GRCh38.p7	7:5624036	TGCTCTGTCCTGGGG[G/T]CCTGGGGAGGGGCAC	54476
rs769294773	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5716432	CCTCGTTAACTCTAA[A/G]GTGATATCTAAGTTG	54476
rs769303185	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5643910	AGGCTAGGCAAATGC[A/C]CATATGCCTCTGATA	54476
rs769313048	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5694634	CCAAGCCAAAGGATG[A/G]GGCCCACTTGTGGCG	54476
rs769314297	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5720413	CTTATTCTAAGAATA[C/T]AGCATGTAATACACA	54476
rs769331092	in-del	-/TTTA			frameshift-variant, intron-variant	RNF216	GRCh38.p7	7:5741807	TCGTGATCTCTGAGG[-/TTTA]TTTGTCTAAGAAAAA	54476
rs769333718	snp	G/T	3.32331e-05	0.0040762	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752896	CTTCATGCTGCTGAG[G/T]AGCTGGGGTGACCAG	54476
rs769344293	in-del	-/GCCCCCCAGGCTGAAGTAATGGTGCGATCTTG			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767636	ATGGAGTTTTGCTCT[lengthTooLong]GCCACCCAGGCTGAA	54476
rs769347457	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5695408	CGGCAGAAGCGCCAC[A/G]TCGCCTTCCTCTCCT	54476
rs769372341	snp	A/G	1.77843e-05	0.00298191	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739283	ATACTTACACATTCA[A/G]ATCATAATAATTCTT	54476
rs769392919	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5661397	TAAAGAAATAAATGA[C/G]ACCTGCTAGGACTGA	54476
rs769396345	snp	A/G			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620440	CTGAAGACCCCCAGT[A/G]CTTCTCTCCCCAATG	54476
rs769434657	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5624511	TCCCAAGTCCACAAG[C/T]GCTCGGCATGGCAGC	54476
rs769438089	snp	A/C/G	8.5769e-05	0.00654813	intron-variant	RNF216	GRCh38.p7	7:5715017	AGACTCCAGGAATGT[A/C/G]TCCTATATACATGGG	54476
rs769460880	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5723153	ATCTCATAAGGCTAT[C/T]TGAAACATAAATGAA	54476
rs769464668	snp	A/T	1.64727e-05	0.00286986	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741497	TGACTTTCTGCTCTG[A/T]TCTGGGGTTGACAAT	54476
rs769481609	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5645902	GCTGGTTTCTTAATT[G/T]CTATCTATACTCTCT	54476
rs769486215	snp	C/G	3.29592e-05	0.00405938	missense	RNF216	GRCh38.p7	7:5641189	AGCATCTTGAACACT[C/G]CTGGCAAGGGGCTCC	54476
rs769508612	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664945	GGGATTACAGGCGCC[C/T]GCCACCAGGCCTGGC	54476
rs769513363	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5764645	AGAGCAAGACACCGT[C/T]TCAAAAAAAAAAAAA	54476
rs769518808	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5706732	TCCTTTCCACCGGCT[C/G]CCTTTTCACTCTGTT	54476
rs769528914	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5631101	ATTCTGAAACCTCCT[C/T]TCTCCCCTTACAAGA	54476
rs769537868	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5743950	AGAGAAACAACATCA[A/T]ACAGAATCCCAAAAT	54476
rs769539473	snp	C/T	1.80478e-05	0.00300392	intron-variant	RNF216	GRCh38.p7	7:5641116	ATATATTTCTATTTT[C/T]TCCCTATAAAGCAAT	54476
rs769550370	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5645387	ATTGGTACATCAGAT[A/G]ATGTTCTACAGGTCC	54476
rs769570154	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5625630	TTGTTTGTGAACCGC[-/A]AGGATTCTGGAGTTA	54476
rs769572532	snp	A/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681799	CAACAGCCATCCCTC[A/T]ATCCTGACTACATAA	54476
rs769599759	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5772900	TCTCCTGCCTCACCC[A/T]CCCGAGTAGCTGGGA	54476
rs769600468	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5734082	AATCTCCAACAAACA[A/G]TTCTGCTGGAAGACA	54476
rs769615962	snp	C/T	3.29837e-05	0.00406088	utr-variant-5-prime	RNF216	GRCh38.p7	7:5761109	GGGACTGCTAATATC[C/T]AAACATGGTGACCAT	54476
rs769617442	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5637026	ACCCTCACGCTAACT[C/G]CCACTCTGCCCTTTG	54476
rs769640575	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5703944	AGAATACATATTCCA[A/G]AAGCATCACCTTCAA	54476
rs769668598	in-del	-/CTCT			intron-variant	RNF216	GRCh38.p7	7:5655715	GTTTAACATTTGGAG[-/CTCT]CTCTGTGTAGTGTCT	54476
rs769669257	snp	A/C/G	4.94306e-05	0.00497124	missense, synonymous-codon	RNF216	GRCh38.p7	7:5761019	TTGTCCCCGATGGCA[A/C/G]TGAAAGTTGTTCAAG	54476
rs769671024	snp	C/T	1.6473e-05	0.00286988	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741413	CTGTCTCTGAGTCTT[C/T]GGATGACTGGTTCTG	54476
rs769706011	snp	A/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664391	AATGAGTTAAACTAC[A/T]AACAGCAGTTATTAC	54476
rs769710724	in-del	-/ACAGAC	1.64836e-05	0.0028708	intron-variant	RNF216	GRCh38.p7	7:5652524	TCCTGGGGATAAAGG[-/ACAGAC]ACAAAGACAACTCCT	54476
rs769719581	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5744271	GATATATAGCATTTT[A/C]AGTAAATACAGTTGA	54476
rs769725260	snp	A/G	8.24477e-05	0.00642005	intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652374	GTTAATGGGGAAGTT[A/G]AGAATCAGCCCATAG	54476
rs769730103	in-del	-/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672725	GAACAGAGAAGGCCA[-/G]GTGAGGAGGCTGCTG	54476
rs769735892	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5708032	ATGCCCGGACAGTGT[C/G]TTTAGTTCTCATACT	54476
rs769737942	snp	C/T	0.000165824	0.00910409	intron-variant, splice-acceptor-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739622	AAATATTGAGCATCT[C/T]TGTCTAGACAAAGGG	54476
rs769755123	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679985	GGGAGTCTCTTGCTG[A/G]GATCATTACATCCTC	54476
rs769780767	snp	C/T	1.67391e-05	0.00289297	intron-variant	RNF216	GRCh38.p7	7:5715225	ACACATGAAATGTCC[C/T]GCACTTAAGGAGAGG	54476
rs769781964	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5698788	GAATCTTGTGCAGAG[A/G]AACTACACAGGAAAC	54476
rs769799311	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5637688	ACACAGGTGTGCACG[C/T]ACCACCACCCCTGGA	54476
rs769804686	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664939	GTAGCTGGGATTACA[A/G]GCGCCCGCCACCAGG	54476
rs769810156	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5747605	AAATTAGAGACAAAG[A/G]TCATGCACGGTGGCA	54476
rs769829611	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5697691	ACAGAAGGTGGGGAA[A/G]GGAAGAATCTTTACA	54476
rs769841278	snp	C/T	1.67466e-05	0.00289362	intron-variant	RNF216	GRCh38.p7	7:5725466	AAAAGGAAAGGTTCC[C/T]TCTGTAAATAGAAAA	54476
rs769876749	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5766350	GATGAGTGATGCTCT[A/C]AAGTGTGTCACGCCT	54476
rs769893553	in-del	-/AAAC			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675000	AGACTCTGTCTCAAA[-/AAAC]AAACAAACAAACAAT	54476
rs769896008	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5735555	GTAGATGAGTTAAAA[A/G]GAGATTACACTCTAC	54476
rs769925786	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5693238	TGGTTACTTTCACGC[C/T]ATAAAGGCAGAGTTA	54476
rs769980198	snp	G/T	3.30764e-05	0.00406659	missense, intron-variant	RNF216	GRCh38.p7	7:5741755	CTCCCAACCTTTTCA[G/T]ATCTTGCCACTGGGC	54476
rs769981023	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5722773	ACGCCTGTAATCCCA[A/G]CACTTTGGGAGGCCA	54476
rs770001833	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5710435	TCTTTGGCCTTCCCA[A/G]TTGTACATAAGCACT	54476
rs770013576	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681036	CTCCAGCCATACCCC[A/G]CAGATACCCCAGACC	54476
rs770024795	snp	A/C/G	4.94412e-05	0.00497178	synonymous-codon, missense, intron-variant	RNF216	GRCh38.p7	7:5741699	AAAATAGCTGCTCTT[A/C/G]TCTGATTCAAATGCT	54476
rs770029020	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5649278	GCGCCTGTAATCCCA[C/G]CTACTCGGGAGGCTG	54476
rs770032230	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5717409	ACTTCGCTGGCGAGG[A/C]TGTGTGGTAGTGGGC	54476
rs770052669	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5690116	GGCGGATCACCTGAG[A/G]TCAGGAGTTTAAGAC	54476
rs770056139	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5683181	AGCTAGAAATGCAGC[A/C]TCACATGGTAGAAGG	54476
rs770060517	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670544	CCTTAGGAGATTCCA[C/T]CATTTCACAGAAATG	54476
rs770131413	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5721272	ATCCTCCACCTTCTC[C/T]CTGATGGTACGTTTC	54476
rs770132402	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5720043	GTGTCTTAAAAATGT[-/A]AAGTGCATGGTGGTG	54476
rs770136857	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5641574	TTCAGTAAATTACTC[A/C]CCTGCCTGGAGACTC	54476
rs770154314	snp	C/G	1.76443e-05	0.00297016	missense	RNF216	GRCh38.p7	7:5623150	CCACAGGCTTCTCCA[C/G]CGGGGGTCCAATGCG	54476
rs770154409	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678557	TACTAAAGTGACCTC[A/G]GGTGAGTGACCTCAC	54476
rs770164077	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5749718	AAGATGTATATGCGA[A/G]AAATGAAACGAACTC	54476
rs770164668	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5705917	CATCTCAACAAAAAC[-/T]AAAACAAAACAAAAC	54476
rs770175788	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741246	GCGGCCCAGTTCTGC[C/T]TCAGGCTGCCGTTCC	54476
rs770191039	snp	C/G/T	3.29469e-05	0.00405864	missense, intron-variant	RNF216	GRCh38.p7	7:5741676	AACAATGGGTTGTTA[C/G/T]ACACTGAAAAATAGC	54476
rs770214884	snp	C/T			utr-variant-3-prime	RNF216	GRCh38.p7	7:5621674	AACCCCATGGCAACA[C/T]GACAAGGACAAGGCA	54476
rs770217523	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5765278	CCAGCCTGGGCAACA[C/G]AGTGAGGACTATCTA	54476
rs770228886	snp	C/G	1.64732e-05	0.0028699	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741179	AAATCCCACCTTGCT[C/G]GGGTTCCGGCCTTGG	54476
rs770286317	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675732	TTTTTTTTTTGAGGT[A/G]GAGTTTCGCTCTTGT	54476
rs770287596	snp	C/T	0.000109776	0.00740781	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5711954	GGACATTCACATCCC[C/T]TTTATACTCCTTAGT	54476
rs770295200	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5624657	GAGAGGAGGAAGGTG[C/T]GACAGTGAGGATGGT	54476
rs770296067	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5642862	CTACAGCACAAACCT[C/T]CTCTGTAAGAGCACC	54476
rs770330490	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5657486	GCAGGAGAATAGCTT[C/G]AACCCAGGAGGTAGT	54476
rs770336191	in-del	-/ACC			intron-variant	RNF216	GRCh38.p7	7:5739230	TATTACATATATTTT[-/ACC]ACCACCACCACCACC	54476
rs770366507	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662951	GGGACAGGACAGAGC[A/G]CTCAGAGAATCCAGC	54476
rs770400291	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5696167	CAGTCCATGTGGTGA[C/T]GAAGAGCAGTTGGTA	54476
rs770440453	snp	A/G	3.29853e-05	0.00406098	intron-variant	RNF216	GRCh38.p7	7:5716781	GCTGAAGAACAAAAA[A/G]GGCACACATTCAGAC	54476
rs770450994	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5774592	GAAAAATCAAAATAG[C/T]TATTCTTACATTACA	54476
rs770460880	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5720468	CTATTATGGGTAAGG[C/T]TTCCTGTCAACGGTA	54476
rs770481973	snp	A/G	1.90893e-05	0.00308938	intron-variant, nc-transcript-variant	RNF216, MIR6874	GRCh38.p7	7:5711853	ACCTAGAGTCAGAAC[A/G]GCAGAACTGACATTA	54476
rs770487412	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5626166	GGTTAACACATAAGA[A/C]TTCTCTATCAAAACC	54476
rs770492496	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5687026	GATAAAAGCAGAGCC[C/G]TGATTATTCTAATTG	54476
rs770522960	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5745106	ACCTGTAAGATCTAC[A/G]GAGAAAACACTAATA	54476
rs770532747	snp	A/C	1.66181e-05	0.00288249	intron-variant	RNF216	GRCh38.p7	7:5730833	CTGCAGAAACAAATG[A/C]TGTTACTTTCATACT	54476
rs770579705	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5758737	GCATGTACCCCCATA[C/G]TATCTTGGGAATAAT	54476
rs770585905	snp	G/T	1.91206e-05	0.00309192	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5730730	CTTTGTCTCATCTTG[G/T]CTGGCCAGCAGACTG	54476
rs770592295	in-del	-/AAT			intron-variant	RNF216	GRCh38.p7	7:5737526	TGATCAATTAAAAAT[-/AAT]AATAATAATAATAAT	54476
rs770596833	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5695572	AGACACCGCAGCTAT[A/G]GACAAGTTCTATTGC	54476
rs770601544	snp	A/G	1.67063e-05	0.00289014	intron-variant	RNF216	GRCh38.p7	7:5725460	ATTGAGAAAAGGAAA[A/G]GTTCCTTCTGTAAAT	54476
rs770615403	snp	C/T			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5621056	GCGCCAGCAAGGACA[C/T]AGCAGCAGGCTGCCC	54476
rs770619949	snp	C/G/T	6.5908e-05	0.00574023	missense	RNF216	GRCh38.p7	7:5761014	TTACCTTGTCCCCGA[C/G/T]GGCAGTGAAAGTTGT	54476
rs770633469	snp	C/T	1.73972e-05	0.00294929	missense	RNF216	GRCh38.p7	7:5624077	TCTTTCTTTTCTGTT[C/T]CTCTTCAGCCTCCTT	54476
rs770634835	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5718925	GGCCTCCCAAAGTGC[A/T]GGGATTACATGCATA	54476
rs770639223	snp	A/G	1.6473e-05	0.00286988	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741407	ACAGCTCTGTCTCTG[A/G]GTCTTCGGATGACTG	54476
rs770642803	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5706405	CTTCTCCCAGCCTCT[A/G]GCACCCAGGGTTCTA	54476
rs770652844	in-del	-/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677024	ATGAAACGAACCTCG[-/T]TAAGAGAACTAACTA	54476
rs770658196	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5656445	TGAAGAACAGGGTAT[C/T]GTGGCCATCGCGCGG	54476
rs770658811	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5645651	GCTGGTGTGCAGTGG[C/T]GCAGTCTCAGCTCAC	54476
rs770679495	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5636609	TCTGAATGGCTTTGT[A/G]TTCTCAGAAGCCCCA	54476
rs770686474	snp	C/T	1.65729e-05	0.00287857	missense, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712778	CGCTCATAGTACTTA[C/T]ACAGGATGGTCTGGG	54476
rs770694080	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672383	CCCACTCTGCAAAAA[C/T]GCCAAGTTGGAGAGT	54476
rs770706076	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5644021	TAGCATGTATCGATA[C/T]TTCATTCCTTTTTAT	54476
rs770712872	in-del	-/TTGT			intron-variant	RNF216	GRCh38.p7	7:5696198	CCGCATGGCTTTAAA[-/TTGT]TTGTATTTCTGTCAG	54476
rs770717520	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5744080	AAACAAATATACAAG[A/G]GTTTCACACAGTGAA	54476
rs770721279	snp	A/C			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753887	GTAATCCCAGCTATT[A/C]AGGAGGCTGAGGCAG	54476
rs770742349	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5778829	GATCACTGCAACCTC[C/T]GCCTCCCGAGTTCAT	54476
rs770774616	in-del	-/GGGGT			intron-variant	RNF216	GRCh38.p7	7:5684910	CTGCATGGGGGGCTG[-/GGGGT]GGGGTGGGGTGTTAG	54476
rs770785618	snp	G/T	3.29625e-05	0.00405958	missense	RNF216	GRCh38.p7	7:5725375	TCATTTGTTTTCTCT[G/T]CTTCCTTTTTCCACT	54476
rs770789072	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5759383	CTCTTCAGCCTACTC[-/A]ATGTGAGGATGATGA	54476
rs770798798	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681024	TCATGCTGCTGCCTC[C/T]AGCCATACCCCGCAG	54476
rs770800866	in-del	-/TCTT	1.64727e-05	0.00286986	frameshift-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741555	TCCAGGCTTGGGTTC[-/TCTT]TCTGTTTGGCCACTT	54476
rs770835110	snp	C/G	1.71035e-05	0.00292429	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5740993	CTTTCACTAGTAGTT[C/G]AACGAGCTCTTGATC	54476
rs770873344	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675290	TGCACAGACAAGAAT[C/T]AGAAGCCCCAGAGGG	54476
rs770888381	snp	A/C			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681822	CTACATAAACGGGAA[A/C]CACCCAGAAAAGGAG	54476
rs770890399	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671190	TCCATGTGCCCATGT[A/G]AAGGCTGGAAATCCT	54476
rs770897672	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5699236	AGATTACAAATCTTT[C/T]CATTTATAAATATTT	54476
rs770917576	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753095	GGCTACTAGTGTAAC[A/G]TACCTCCTCAAGCAG	54476
rs770919675	snp	C/T	1.70168e-05	0.00291687	intron-variant	RNF216	GRCh38.p7	7:5725300	GTTGCAGCTACACAC[C/T]GCCACCAACACAGTT	54476
rs770920276	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5746604	AACTGCAAAGTGATT[G/T]GCTAGGTAGGACATC	54476
rs770928352	snp	C/T	1.64781e-05	0.00287033	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5729551	TGAAGCAGCGCTGGT[C/T]AAGAGGGGTCAATTT	54476
rs770938855	snp	C/G			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620504	GGCCCTGCCTCTGGA[C/G]AGAGGGGCCTGGAGA	54476
rs770939477	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5630446	AAAATGGCGTGATTA[C/T]AGCTCACTGCAGCCT	54476
rs770964144	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5729409	AAGAGGTGTGACCCC[A/T]ACAGGAAGACCAAGT	54476
rs770964244	in-del	-/GAGGTGA			intron-variant	RNF216	GRCh38.p7	7:5632443	GAGCAAGGCCAGGCT[-/GAGGTGA]GAGGGAGTGGATGCT	54476
rs770976751	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5709376	CAGCGTCACAAATTC[A/C]CCAGCCTTTGATGCA	54476
rs771029566	snp	A/G	6.85542e-05	0.00585426	missense	RNF216	GRCh38.p7	7:5622876	CAGAAGCGATGCCGC[A/G]GCTGGGGGCCAAAGT	54476
rs771033428	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5724079	GTGAGATGCAGCAAA[A/C]CTGAGACAGGTTTAT	54476
rs771034520	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5740874	TTAGGAAAATGAAGT[-/C]CACGCATACCAACAA	54476
rs771046250	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665050	TGATCTGCCCGCCTC[C/G]GCCTCCCAAAGTGCT	54476
rs771083367	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5718368	CCTGGGTGACAAAGC[A/G]AGACTCCGTCTCAAA	54476
rs771090256	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673601	CACAGCCCAGAATGA[A/G]GGTCTGCAAGGAATT	54476
rs771092760	snp	C/G	1.64942e-05	0.00287173	missense	RNF216	GRCh38.p7	7:5715136	CTGCGCACTGCGTCA[C/G]CTCCTCGAATGGAAA	54476
rs771112859	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5700179	TGGAAGGCTGGAAAC[C/G]CTGCAGTGCTCTGTG	54476
rs771124499	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5773000	GGCCAGGCTAGTCTC[C/G]AACTACTGACCTCTG	54476
rs771129641	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5656453	AGGGTATCGTGGCCA[A/T]CGCGCGGGACCACAC	54476
rs771135918	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5639389	CTTACACATAGAGGA[A/G]AAACACACTTCTGTT	54476
rs771144096	snp	C/T	1.68872e-05	0.00290574	intron-variant	RNF216	GRCh38.p7	7:5715043	ATGGGACATATTACA[C/T]AGTTCTTACCTTTCC	54476
rs771145542	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5747097	CTGAATATTCACAGT[A/C]TACTAACTCTGAGTT	54476
rs771159855	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5776594	GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	54476
rs771185779	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5645076	TGCCTCAGCCTCCCA[A/G]AGTACTGGGATTACA	54476
rs771209374	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5746806	AAATAATTCAGAATT[-/A]TGATGACCATGATGT	54476
rs771216799	snp	A/G	1.88977e-05	0.00307384	stop-gained, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711766	GCCTCCCTACCTTTC[A/G]GCAGTGAGGATTAGG	54476
rs771228738	snp	C/T	4.94254e-05	0.00497094	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741105	TTCATCATCACTTGC[C/T]AACTGCTGGTCTTCA	54476
rs771234199	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5638909	CAAAGCTTACAGACA[C/T]GAGCCACTGCACCTG	54476
rs771293921	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5623623	TAAAGAAAAACAGAT[A/G]GGGTCTTGCTATTTT	54476
rs771302227	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5741878	TCCCTCCTTATGTAC[C/T]TATATTGAGCTTCCG	54476
rs771303065	snp	G/T	3.29457e-05	0.00405854	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741175	CCTGAAATCCCACCT[G/T]GCTGGGGTTCCGGCC	54476
rs771321382	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5729127	TGACCTGTCCCAAGT[C/T]GGAAAGCAAATCAGG	54476
rs771332201	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5638474	CTTCGGATCTGTACA[C/G]AGTAACTGCCCACTA	54476
rs771343982	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5755803	TAGCTGGATACATTC[C/T]AGGAGTGGAAATGCT	54476
rs771366382	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5643240	GCTTCTGCATTTGTA[A/G]GAGTAGTACTGGATA	54476
rs771391003	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5684428	CTGGGCCTTCTAAGC[C/T]GAGCCTCTGCATTAA	54476
rs771396617	snp	C/T	1.64741e-05	0.00286998	synonymous-codon	RNF216	GRCh38.p7	7:5721051	TGCCATCTCTTTGAT[C/T]TTCTGCTCATAGAAC	54476
rs771408511	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5633941	CACAGTTCTGTCCAC[A/G]CAGCAGGGTATAGAC	54476
rs771414489	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679670	ATCGAGAGAATAGCC[C/T]TGTCATGGAATCTCC	54476
rs771416517	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668942	TTCACACCTTCACTC[A/G]TCCCCACAGGGCTCT	54476
rs771418530	in-del	-/A	2.06098e-05	0.00321006	intron-variant	RNF216	GRCh38.p7	7:5641424	GGGAAGATGAGGAGG[-/A]AAAAAATATGGCCAT	54476
rs771428845	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5626484	ACTGATCCAGAAAAC[C/T]GGTGGGAGGATCACT	54476
rs771442094	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5632892	AATGGCACCACAGTG[A/G]GCAGTGCACCCCAAA	54476
rs771473077	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5760897	TCAAAAACGAAATGT[C/T]CCTGGATTCTAAATG	54476
rs771498706	snp	A/G	1.65121e-05	0.00287329	missense	RNF216	GRCh38.p7	7:5623165	GCGGGGGTCCAATGC[A/G]TTTGAAGGTGTTCTC	54476
rs771501726	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5702072	AGGCCCCAGGTCGCT[A/G]CCGGGTTCTCGGAGC	54476
rs771503307	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5692718	ACACACCAGAAGAAA[C/T]AGCTTGGAGTTTGAA	54476
rs771522627	in-del	-/A/AA			intron-variant	RNF216	GRCh38.p7	7:5647119	AAGTTGTGAAAGGTG[-/A/AA]AAAAAAAAAAAGGGA	54476
rs771525128	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5633067	TCACTGCAACCTCCG[C/T]CTCCCGGGTTCAAGT	54476
rs771562315	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5688075	AACCGAAGAGGTAAT[C/T]AGAGCAGTAAATAAG	54476
rs771572320	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5626304	AGGGTTGGGTGGGCA[A/G]TTTGAAGGCCTCCAT	54476
rs771574713	snp	C/T	3.59667e-05	0.00424052	missense	RNF216	GRCh38.p7	7:5624058	GAGGGGCACTTGCCT[C/T]CATTCTTTCTTTTCT	54476
rs771584009	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5750641	AGTCTCATGCCTAAT[A/G]CATGGGCCACACAGA	54476
rs771585227	snp	C/G	1.859e-05	0.00304871	intron-variant	RNF216	GRCh38.p7	7:5729644	CAGGCAGTACATTTC[C/G]CATACAGGGGAAATC	54476
rs771587648	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5702985	GGCACCCTACATGAT[A/C]TACCTGTAAGGGAGC	54476
rs771640025	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5771831	CCCAAAGGAAAAATG[C/G]GGCAAACAATTTGAA	54476
rs771646715	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670968	CCTAGAGTGTTTTCT[C/G]TGAACTGCTTGGTTC	54476
rs771653100	snp	C/T			intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652326	TCAAGCGTGTTCTTC[C/T]GACAACAGTATGCCC	54476
rs771661826	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5637579	TGAGACATGGTCTCA[C/T]TCTGTCACCCAGGCA	54476
rs771661900	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5733034	CGGTTCCATCTGAAG[C/G]CCATTTAAAGATGCA	54476
rs771676531	snp	C/T	1.6507e-05	0.00287284	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712690	GGAAGAGTTGGCAGA[C/T]GGCACGCTCTGCCTG	54476
rs771680151	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5775989	TTTAAAAATGTCTAT[A/T]AACGATTGTTTTTCA	54476
rs771683505	snp	A/G	3.29468e-05	0.00405861	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741389	ACTCTCCTAGATTTG[A/G]TAACAGCTCTGTCTC	54476
rs771721295	snp	C/T	1.73261e-05	0.00294325	missense	RNF216	GRCh38.p7	7:5622873	CATCAGAAGCGATGC[C/T]GCGGCTGGGGGCCAA	54476
rs771734800	snp	C/T	1.64741e-05	0.00286998	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741326	GGAAGTAAGGATGAT[C/T]TAACCAGCAGTCTTC	54476
rs771736298	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5710570	CACCTGGACTACTCA[A/G]TAGGCAAGTAGACTT	54476
rs771742659	snp	C/G	1.64776e-05	0.00287028	missense	RNF216	GRCh38.p7	7:5761009	ACAACTTACCTTGTC[C/G]CCGATGGCAGTGAAA	54476
rs771766081	snp	C/G/T	3.29648e-05	0.00405974	missense	RNF216	GRCh38.p7	7:5725368	TACTGGTTCATTTGT[C/G/T]TTCTCTTCTTCCTTT	54476
rs771767628	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677217	GTGATTTAGAGACTG[C/G]TCAGCACGTGCTTCT	54476
rs771769619	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5774001	TAAGCAGACTGCTAG[-/T]TAACGGTTCAAAAAA	54476
rs771795303	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5627558	AGAGATCATCCTGGC[G/T]AACACGGTGAAACCC	54476
rs771796070	snp	C/T	0.000209666	0.0102366	intron-variant	RNF216	GRCh38.p7	7:5760512	TGAGTAAAATTCCAT[C/T]TCAAAAAAAGAAAAA	54476
rs771799564	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5721349	ACCATTAGCCAACCT[A/C]CCATCCATTTTTTGA	54476
rs771813185	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673213	GGAAGTCAGTGGTTA[C/T]TGAGATTCTTCTATG	54476
rs771818999	snp	C/G	1.71953e-05	0.00293212	intron-variant	RNF216	GRCh38.p7	7:5725292	GGTACAGTGTTGCAG[C/G]TACACACTGCCACCA	54476
rs771831695	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5696322	AGAAATTAAGCTGAT[C/T]TGAGTGAGAGAAATT	54476
rs771846982	in-del	-/TT			intron-variant	RNF216	GRCh38.p7	7:5774793	GACGAAGTTTTGCTC[-/TT]GTTGCCCAGGCTGGA	54476
rs771849685	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669878	GCCTGGGCAAGACTC[C/T]ATCTCAAAAAAAAAG	54476
rs771851078	snp	A/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663131	GCTCCCACAGCACTT[A/T]GCTTATGCGTTGTTA	54476
rs771858096	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5636805	TTTGAGCAAATCTAG[A/C]AACTTTCTCAGGTTA	54476
rs771876955	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5720920	TTGCATATATCCAAA[C/T]TTAACAGTCTGAAGA	54476
rs771910390	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5750054	CCTCCAGAATTTGCA[A/C]ACTATTCATGAGTAT	54476
rs771925449	snp	A/C	1.7154e-05	0.0029286	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739334	TAAACCCATTTGCTA[A/C]ATCTGGAAATCTTGC	54476
rs771977208	snp	C/T	1.64765e-05	0.00287019	missense, intron-variant	RNF216	GRCh38.p7	7:5741688	TTACACACTGAAAAA[C/T]AGCTGCTCTTATCTG	54476
rs771983037	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666345	GGGGAAATAGTTCAC[A/G]ATTATAAACTGGTGG	54476
rs771989048	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5708161	ATTATGATCTAATAT[A/T]CTCCATCCTGGAAAA	54476
rs771991598	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5725536	AACACAGTTTCAGCT[A/G]TCTACCCAGCATGGC	54476
rs772002281	snp	G/T	1.64963e-05	0.00287192	intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652366	AAAAGCAGGTTAATG[G/T]GGAAGTTGAGAATCA	54476
rs772012394	snp	C/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753971	CTGCACTCTAGCCTG[C/G]GTGACAGAGTGAGAC	54476
rs772020531	snp	A/T			upstream-variant-2KB	RNF216	GRCh38.p7	7:5781931	GGCAGGTGGTTGTGG[A/T]TGTTTACTCGATATC	54476
rs772043611	snp	C/T			intron-variant, nc-transcript-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662496	CATTGCTTGAGATTA[C/T]CACCATCACTGAAAC	54476
rs772053903	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5745323	AGTCAAAGTAAATGA[C/T]TAGTTCCTTAACATA	54476
rs772054033	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5646583	CTGTAGTCCCAGCCA[C/G]TCAGGAGGCTGAGGC	54476
rs772061212	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681946	AAAGAATGCTACAAA[A/G]ATGACCATCTCCCTG	54476
rs772061680	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5707530	AGTTTTTTTGTGGAA[A/C]TTGCAGATTTTTCTA	54476
rs772077768	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5705571	TCACTCATGCTGCAC[A/G]TCCCTCTTGGCAGAG	54476
rs772108586	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5698471	CATGGTTCACAGCGG[C/T]CTCGATCTTCTGGGC	54476
rs772109184	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5690617	TCTGCAAGCATCACA[C/T]AACCCTAAATAGTAA	54476
rs772134704	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5685071	CTGGATGAAGGCAGC[A/G]TCTTGCCTGCCCTCA	54476
rs772171212	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5736353	TCTCCAGCTCCTAAC[C/T]GGGACTGATCTGCCA	54476
rs772180514	snp	G/T	1.64852e-05	0.00287094	synonymous-codon	RNF216	GRCh38.p7	7:5641322	TTCAGATTTGATGAG[G/T]CCAGTCCCACACTTG	54476
rs772185857	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5739902	CAGCTACTCGGGAGG[C/T]AGAGACAGAAGAATC	54476
rs772212483	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5764150	GTAAGCTGAGATCAC[A/G]CCATTGCACTCCAGG	54476
rs772215893	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5686719	ATATTACCTACAGAA[C/G]ATCTTAAAACAGCGG	54476
rs772216616	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667506	TGCCCGGGAACCAGG[A/G]GAACCCCCCAGCCTT	54476
rs772242508	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5640623	ATTTGATTTCTTAAA[C/T]GTCTTCTCACCATCT	54476
rs772243747	snp	C/T	1.64749e-05	0.00287005	missense	RNF216	GRCh38.p7	7:5729451	CGGGTGATTGCATAG[C/T]GTCCTTTGAGCTCGT	54476
rs772245818	snp	C/G	5.38353e-05	0.00518794	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712874	TCCAACTAGAAAAAG[C/G]CGAAAAGGCAAAGAA	54476
rs772250319	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5752742	GGGCTGTTCTCAGAA[A/C]GAGTACAAGAGGTGC	54476
rs772258838	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673816	CAGGAGTTTGAGACC[A/G]GCCTAGGAAAGATAG	54476
rs772273691	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5709486	CTGGAGCTTTCTCTT[C/G]TGTCATCTTGACACT	54476
rs772284581	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5631783	CCTCACCAGAGATCA[A/G]TCCTGGGAACATTCT	54476
rs772296161	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5736679	TAGGAAGTGAGGAGC[A/G]TCTCTGCCGGGCCAC	54476
rs772296930	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5773853	ATAACAGGCGAGTCA[C/T]CGTGCCTGGCCCCAA	54476
rs772298697	snp	C/T	3.35886e-05	0.00409795	intron-variant	RNF216	GRCh38.p7	7:5725471	GAAAGGTTCCTTCTG[C/T]AAATAGAAAATAAGA	54476
rs772311759	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5773721	CGACACATGCGTGCC[A/C]CCATGCTGGTTAATT	54476
rs772314921	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5639541	CGATCTCAGCTCACT[A/G]CAACCTCCGCCTCCT	54476
rs772336749	snp	A/G	1.64876e-05	0.00287116	missense	RNF216	GRCh38.p7	7:5716766	GCAAAAAGTCTTCAT[A/G]CTGAAGAACAAAAAA	54476
rs772343425	in-del	-/T	1.64792e-05	0.00287042	frameshift-variant	RNF216	GRCh38.p7	7:5761069	TGTTTCCCTCTTCCA[-/T]TTTCAAATGCAGACA	54476
rs772359168	snp	A/G	4.97946e-05	0.00498947	missense, intron-variant	RNF216	GRCh38.p7	7:5741784	GCAGCTGGTTTGATG[A/G]GATTGGGTCGTGATC	54476
rs772363229	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5647710	CTAGAAGCCTGAGAA[C/T]CATTCTAGACTCCTT	54476
rs772384746	snp	A/G	1.64879e-05	0.00287118	intron-variant	RNF216	GRCh38.p7	7:5652532	ATAAAGGACAGACAC[A/G]AAGACAACTCCTGGT	54476
rs772437508	snp	A/G	1.64789e-05	0.0028704	intron-variant	RNF216	GRCh38.p7	7:5721018	ACACCCCAAGACCAG[A/G]GCACATCTTCCTACC	54476
rs772462682	in-del	ACATTAACCAAAAAAAAAAAAAAA/CATT			intron-variant	RNF216	GRCh38.p7	7:5733655	TTCATAACCAGGAAA[ACATTAACCAAAAAAAAAAAAAAA/CATT]AGGAATTCAAAGAGA	54476
rs772470401	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5694284	TCTAGGTATGCAGTA[C/G]TTGAATCATTCACAC	54476
rs772484246	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5693256	AAAGGCAGAGTTAGG[C/T]AGCTGGGATAGATAC	54476
rs772498990	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5718622	CATGATTTTGGCTCA[C/T]TGCAACCAACCTCGA	54476
rs772517763	snp	A/T	1.9228e-05	0.00310059	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5730716	AACATGACACTTGCC[A/T]TTGTCTCATCTTGGC	54476
rs772518658	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5650123	TTCTGGTGGTCTGGA[A/G]GTCAGGCATGTATAT	54476
rs772530931	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5627095	GACACTTATGGCCTT[C/T]GATGGCACAAGGGGG	54476
rs772533860	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5729803	ACAGACTAGTTTTAC[C/T]ACTAAAGAAGTATAG	54476
rs772556619	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5757059	TTCAAAATATCTTCT[A/G]ATTTTCATTGTGATT	54476
rs772564320	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5659730	ATTTGATTCTTGCTT[A/C]GATTTCCTCAACAGT	54476
rs772564837	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5661455	TTTGCATACACATCT[C/T]AATCTTCACAGCAAC	54476
rs772566320	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670921	AAGGTCTTCCCAAGA[C/T]GAACCACCATGCCTC	54476
rs772572280	in-del	-/CA			intron-variant	RNF216	GRCh38.p7	7:5640907	GAATATTTCAGAGGG[-/CA]CAGAGTTTTATTTCC	54476
rs772581208	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5745264	TAAGATGCTGAAATT[C/G]AATGTAACAGAATCC	54476
rs772605866	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675621	GCTCCAGCCTGGGTG[A/G]CAGAGCAAGACCCTC	54476
rs772607790	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5685944	GTAAAAAATTCCGGC[C/T]GGGCGCGGTGGCTCA	54476
rs772623870	snp	C/T	1.76811e-05	0.00297326	synonymous-codon	RNF216	GRCh38.p7	7:5624066	CTTGCCTCCATTCTT[C/T]CTTTTCTGTTCCTCT	54476
rs772631558	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5756895	CCCACTTTGGCCTTC[A/C]AAAGTGCTGGCATTA	54476
rs772652449	snp	C/G	1.87198e-05	0.00305933	intron-variant	RNF216	GRCh38.p7	7:5729645	AGGCAGTACATTTCC[C/G]ATACAGGGGAAATCA	54476
rs772655188	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5743853	TCCCAGGAACTGAAT[C/T]GCAGCGTGGAGAGTT	54476
rs772655200	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5729270	ATTTCTTTTCATTTA[A/G]TCCGTCACGATGAGC	54476
rs772656158	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5764700	ACTAAAGTAATAAAA[C/T]ATGATCTTTAGGTAG	54476
rs772689049	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5725665	CACCAGTCTGGCCAA[-/C]ATGGTGAAACCCTGT	54476
rs772701134	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5695411	CAGAAGCGCCACATC[A/G]CCTTCCTCTCCTGTT	54476
rs772730250	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5743995	ACTTACACTCAATCA[A/C]AAATAACTAGGCATA	54476
rs772740383	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5746910	AGAACGAGATTCTTA[A/C]TGGCATTCAGAAGCC	54476
rs772752471	snp	G/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767733	CCTCCTGAGTAGTGG[G/T]GACTACAGGCACACG	54476
rs772754357	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5748499	TCTTGGCCTTGGCCT[C/T]CCAAAGTGCTGGGAT	54476
rs772766232	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5650312	CAGGTTTAAATAGGA[C/G]CCAGTGGTGGGCTAT	54476
rs772807468	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5704387	TCATGTCTTAAATAT[C/T]AGGAATCCTCAAGGA	54476
rs772808384	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5768990	AATCCACACATTAAC[A/G]AAGAAATTACAATGA	54476
rs772812331	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5635163	TGCCTCCCAGTCCCA[G/T]GCAGTAAAAATCACA	54476
rs772827008	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5757869	ATAAAAAATTATTAA[C/T]GTTGGCCAGGAGCAG	54476
rs772835163	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5778774	TTTGAGACGGAGTCT[C/T]GCTCTGTCACCCAGG	54476
rs772851811	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670358	ACTGCAGAGGACCCA[A/G]CCATGTGATAGTGGG	54476
rs772855268	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5627608	AAAAATTAGCTGAGC[A/G]TGGTGGTACACGCCT	54476
rs772857896	snp	A/T	1.80807e-05	0.00300667	missense	RNF216	GRCh38.p7	7:5623177	TGCGTTTGAAGGTGT[A/T]CTCTGAAAGGGATGT	54476
rs772862807	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5643112	AAAATGGACAGAGGA[A/C]TACATAAAGCATGCC	54476
rs772868322	in-del	-/T/TTTTTTTTTTTTT			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675714	ACTCTATTCAAATTC[-/T/TTTTTTTTTTTTT]TTTTTTTTTTTTGAG	54476
rs772869427	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5719687	GATGGATCAAAACAA[C/T]AAATTCTAATTTCTG	54476
rs772899066	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5694664	GCAATTTGAGGACCT[C/G]CCTGCCCTGGAGCAG	54476
rs772899081	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5705280	ATGTCCAAAACAAAA[C/G]TAATCTCTCCTGAAT	54476
rs772931298	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680922	TCTAACCCACTCCTA[C/T]CTGGGTCCAAAACCC	54476
rs772966098	snp	A/C	1.64743e-05	0.00287	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741335	GATGATCTAACCAGC[A/C]GTCTTCTTCGATGGC	54476
rs772986987	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5698960	CCCCAAGAGTGAACT[A/G]GAAAGCAGCAAAGCA	54476
rs773015457	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5634599	GGAGCAGAGACTTCA[C/T]GGGCTCAGGGCTGGC	54476
rs773016918	in-del	-/GGTGTGTG			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754119	GTTTTTCTTTTGTGT[-/GGTGTGTG]TGTGTGTGTGTGTGT	54476
rs773017477	snp	C/T	1.6473e-05	0.00286988	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741258	TGCTTCAGGCTGCCG[C/T]TCCTGAGGAACGACC	54476
rs773034443	snp	A/C/G	3.2955e-05	0.00405914	missense, intron-variant	RNF216	GRCh38.p7	7:5741691	CACACTGAAAAATAG[A/C/G]TGCTCTTATCTGATT	54476
rs773037026	snp	A/C	0.00011993	0.00774277	intron-variant	RNF216	GRCh38.p7	7:5725295	ACAGTGTTGCAGCTA[A/C]ACACTGCCACCAACA	54476
rs773052581	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5653883	CAAAGCCGGGCATGT[A/T]CAGTTCCTATGGCTG	54476
rs773073410	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713769	GACATTTTAAAAATA[A/G]CTAGCTAAAATTTAT	54476
rs773075860	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664526	AAGTTGATCTCTCTT[C/T]AATCAGGATAAAAGG	54476
rs773078839	snp	A/C	6.65613e-05	0.00576855	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753005	GCAGAGAACACTGTT[A/C]CTGGGAGGTTGGCAC	54476
rs773102249	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5743130	GCTGGACATGGTGGC[A/G]TGTGCCTGCAATCCC	54476
rs773127617	in-del	-/A	0.000746803	0.0193092	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712887	GGCGAAAAGGCAAAG[-/A]AAAAAAAAATCAATA	54476
rs773128891	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5643992	TGTGTTGTTTTCTAG[A/G]TTCACCTATGTTGTA	54476
rs773131915	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5725507	CGAGACAGGCAATCC[C/G]TGAATGCCATTTTAA	54476
rs773139481	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5761565	GGCCGAGGCGGGCAG[A/G]TCATGAGGTTAGGAG	54476
rs773143600	snp	C/T	1.72749e-05	0.0029389	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739349	CATCTGGAAATCTTG[C/T]TTCCTAGAAACAAAT	54476
rs773188606	in-del	-/GAAA			intron-variant	RNF216	GRCh38.p7	7:5776952	AGAGAGAGAAAAAAA[-/GAAA]GAAAGAAAGAAAAAG	54476
rs773191940	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666734	AGGGGAGGCTGTGAC[C/T]AAGCCCCTTCCAAAG	54476
rs773193731	snp	A/G			upstream-variant-2KB	RNF216	GRCh38.p7	7:5782297	CGGAGGTTGTAGTGA[A/G]CCAACATGGCGCCCC	54476
rs773219561	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5778144	AATCCTTACCATGGC[A/C]TACAAAACGCTACCA	54476
rs773250624	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5772914	CTCCCGAGTAGCTGG[A/G]ATTACAGGCATGCGC	54476
rs773262303	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5683291	AAACAAAAGACCTTG[A/C]TGGATTTTGTTTTAT	54476
rs773266546	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5723204	GAAAAGTGACTGGTA[C/T]ATATTAAGTGCTCAA	54476
rs773271542	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5645985	CACCTGGCTTTCTGA[A/G]CATATTTAAGACAGC	54476
rs773290213	snp	C/T	4.94303e-05	0.00497119	missense	RNF216	GRCh38.p7	7:5761042	TGTTCAAGTGAATTA[C/T]CTCTTCATTGTTGTT	54476
rs773316583	snp	C/G	3.29522e-05	0.00405894	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741089	AGGCTGGACCTGGCT[C/G]TTCATCATCACTTGC	54476
rs773321420	snp	C/T			upstream-variant-2KB	RNF216	GRCh38.p7	7:5782683	GGTGAAACCCCGTCT[C/T]TACTAAAAATACAAA	54476
rs773335431	snp	C/T			upstream-variant-2KB	RNF216	GRCh38.p7	7:5783476	TGCTGTGAGCTATGA[C/T]TGCACTGCTGCACTC	54476
rs773335873	snp	C/T	1.69885e-05	0.00291444	intron-variant	RNF216	GRCh38.p7	7:5641128	TTTCTCCCTATAAAG[C/T]AATAGGCAGCCATGT	54476
rs773371606	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5746911	GAACGAGATTCTTAC[C/T]GGCATTCAGAAGCCT	54476
rs773381311	snp	C/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753055	AGTTTTTCCTGACAG[C/G]GGTACAGCCTAAAGC	54476
rs773382254	snp	A/T			missense, intron-variant	RNF216	GRCh38.p7	7:5741802	TTGGGTCGTGATCTC[A/T]GAGGTTTATTTGTCT	54476
rs773411335	in-del	-/TTT			intron-variant	RNF216	GRCh38.p7	7:5774761	CCATTCCAAGTTACT[-/TTT]TTTTTTTTTATTGAG	54476
rs773414926	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668867	ATCTTTACTACGGGA[A/G]ATAGTAAAACACTAT	54476
rs773420580	snp	C/T	1.71182e-05	0.00292554	intron-variant	RNF216	GRCh38.p7	7:5715023	CAGGAATGTGTCCTA[C/T]ATACATGGGACATAT	54476
rs773437997	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5693282	GATACCATATGGTCC[A/G]CAAAGCCTGAAATAT	54476
rs773463246	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5638463	ACGCACTACATCTTC[A/G]GATCTGTACACAGTA	54476
rs773471407	snp	G/T	1.64741e-05	0.00286998	missense	RNF216	GRCh38.p7	7:5729456	GATTGCATAGTGTCC[G/T]TTGAGCTCGTGCAGG	54476
rs773477257	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5701743	ATGCAGCAACAGCCA[A/C]GCATTTCACTGCCAT	54476
rs773479514	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5722854	TGGTGAAACCCCCCA[G/T]GCATGATGGCGCACA	54476
rs773500706	snp	C/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754884	AATACAAAAATTAGC[C/T]GGGTGTGGTGGCATG	54476
rs773512217	in-del	-/CTGTAAGAG			intron-variant	RNF216	GRCh38.p7	7:5642865	CAGCACAAACCTTCT[-/CTGTAAGAG]CACCCTGAGGCTGAG	54476
rs773515449	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5771944	AAATGTAAACTAAAA[C/T]CACAAGGGGCCGGGC	54476
rs773524637	in-del	-/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753534	CAAGTTTCCTTTAAA[-/T]ATATATATAATCTAA	54476
rs773529685	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5684395	TACAGGTGCGAGCCA[C/T]TGCGCCTGGCCCACA	54476
rs773538076	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5708044	TGTGTTTAGTTCTCA[C/T]ACTTTGTGAATTTTC	54476
rs773544377	in-del	-/CA			intron-variant	RNF216	GRCh38.p7	7:5769919	GCGAGTGCTTGTAGC[-/CA]GGAGGCTGAGACAGA	54476
rs773550601	snp	C/T	0.000104753	0.00723639	intron-variant, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711757	AAAAAATGTGCCTCC[C/T]TACCTTTCGGCAGTG	54476
rs773567481	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5746480	TACCAGCTGTGTTGA[C/G]TGCAGGGAGGGTATA	54476
rs773579532	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5636482	AACTTCCCTCCAAAA[-/C]CATGATGGGACAACT	54476
rs773589424	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5716593	TAACTTGGCTGAACT[A/G]CAAACTCACCAAACA	54476
rs773603934	snp	C/T	1.64936e-05	0.00287168	intron-variant	RNF216	GRCh38.p7	7:5652540	CAGACACAAAGACAA[C/T]TCCTGGTGAGTGGAC	54476
rs773613770	in-del	-/AA			intron-variant	RNF216	GRCh38.p7	7:5746735	TGCCTTTTCATGTAT[-/AA]AACTTCTGGCTCCAG	54476
rs773614158	snp	G/T			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622615	GGTGGCCTGGGGGAT[G/T]CGAGGGGAGGGGCAG	54476
rs773639292	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5688532	TCCCCTCTTGTCAAG[A/C]CTTCCTGTAGCAGTT	54476
rs773659215	snp	C/T	1.6473e-05	0.00286988	missense	RNF216	GRCh38.p7	7:5652435	TACGGTACTTGATGT[C/T]GTCTTTTTCAGCCAG	54476
rs773688964	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5749066	CTAACTCCAATGCCT[C/T]TTAGTTCACGTGACT	54476
rs773715901	snp	A/G	3.29853e-05	0.00406098	intron-variant	RNF216	GRCh38.p7	7:5716777	TCATGCTGAAGAACA[A/G]AAAAGGCACACATTC	54476
rs773724510	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5632248	GCTGCCACAGATCCA[C/T]GACAGACCATGGTGC	54476
rs773742542	snp	C/G	1.66029e-05	0.00288117	missense, intron-variant	RNF216	GRCh38.p7	7:5741785	CAGCTGGTTTGATGA[C/G]ATTGGGTCGTGATCT	54476
rs773745620	in-del	-/G			intron-variant	RNF216	GRCh38.p7	7:5773861	CGAGTCACCGTGCCT[-/G]GCCCCAAGCCAAATT	54476
rs773773199	snp	C/T	1.92018e-05	0.00309847	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5730721	GACACTTGCCTTTGT[C/T]TCATCTTGGCTGGCC	54476
rs773773896	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5647034	TACTCATTGCCTCAG[A/G]CAGCTGCAGCTGGTA	54476
rs773779084	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5641852	CCAGCCTGACCAACA[C/T]GGTGAAACTGTCTCT	54476
rs773781502	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5764554	TCAGGAGGTTGAGGC[A/G]AGAGAATCGCTTGAA	54476
rs773826803	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5748812	AAAAGTTATATGCAG[A/G]TTTTAAACTGCACAG	54476
rs773897679	in-del	-/GGCCGCGCTCGGGTGCACGGACACCGCCTCCGCGGCGGCCTCG			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5781159	CCCGCCGCTCCTCCA[lengthTooLong]GGCCCGGGGGAGGGA	54476
rs773900821	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5688981	TAGGTAAAGGAAATA[C/G]TCCTTTTTCTTCAAG	54476
rs773915416	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5702042	CCTAGGGATCAGGGA[A/G]GTCGGCGACATCTGA	54476
rs773919646	in-del	-/AACT			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677031	CGAACCTCGTAAGAG[-/AACT]AACTAGTGGCCTGAC	54476
rs773927811	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5696238	CATGGAAAAAAAGCA[C/G]GGCTCTCAGCAGCTG	54476
rs773952819	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5749858	TTACATGAGACTGAA[C/T]TGATAAAAGAAGAAT	54476
rs773953859	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5758851	GAATGAGTTAAGACT[C/T]TGGGGACTGTTGGGA	54476
rs773954480	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5778540	CCAAAGTGTCACTTG[A/T]TCCCAAAGCCCCAGG	54476
rs773973624	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5631412	CTAAGCTGCACATGG[G/T]GGCCCAGCACTGAGG	54476
rs773974718	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5648386	TGCTGGGGTTACAGG[A/C]GTGAGCCACTGTGCC	54476
rs773985184	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5736230	CTGCCTGATTCTCCT[A/G]CCTCAGCCTGCCGAG	54476
rs773994605	snp	A/G	1.79171e-05	0.00299303	synonymous-codon	RNF216	GRCh38.p7	7:5623163	CAGCGGGGGTCCAAT[A/G]CGTTTGAAGGTGTTC	54476
rs773994931	in-del	-/CAGT			intron-variant	RNF216	GRCh38.p7	7:5729911	AATACGTAAGAGAGA[-/CAGT]CAAAGAATCTATGGG	54476
rs774005240	snp	A/T	0.000120594	0.00776417	intron-variant, nc-transcript-variant	RNF216, MIR6874	GRCh38.p7	7:5711877	GACATTACTTCAAAC[A/T]TTAAAGCCTGATCTG	54476
rs774010533	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5710734	TTTCTCCATCTCCAC[C/T]CCACTCCCACCCTTT	54476
rs774023078	in-del	-/AA/AAA			intron-variant	RNF216	GRCh38.p7	7:5765968	AAAAAAAAAAAAAAG[-/AA/AAA]AAAGAAAGAAATAGA	54476
rs774023119	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5698218	ACACTCAAAAGGTCA[C/T]GTGGGCTTTCTTCTG	54476
rs774027868	in-del	-/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678897	CCGAGCTCCTAGAGA[-/G]GAAGTGGGGAGCATG	54476
rs774039619	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5625520	GTAGAAGATGGGCAG[A/C]CCCATCGAGGGCTAA	54476
rs774052617	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5690397	GCATGGTTAGCAATG[C/T]TCAGAAGCTAGGTCA	54476
rs774053707	snp	C/G	1.66974e-05	0.00288936	missense	RNF216	GRCh38.p7	7:5623095	TGTGGCAGGTTCTGC[C/G]GAACGGGCCTCGGGA	54476
rs774055422	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5750546	TTTTTATTATCTACC[C/T]GTTAGATAGCAGGAA	54476
rs774056086	snp	A/T	1.65116e-05	0.00287324	synonymous-codon	RNF216	GRCh38.p7	7:5721171	TTCTATTTTTATGTC[A/T]CCTAGAAGATATACG	54476
rs774074866	snp	C/T	1.64727e-05	0.00286986	synonymous-codon	RNF216	GRCh38.p7	7:5721069	CTGCTCATAGAACTC[C/T]TGCTCTTGTTGCACA	54476
rs774075389	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5744147	GGGAAATCAAAGACT[A/G]GATTGAGAACTGCAG	54476
rs774080786	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5650342	TGTGTGGCAGACCAA[C/G]ACGCTGAGCGGAACC	54476
rs774084531	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5661663	CAAAAATTAGCCAGG[C/T]GTGGTGGTGCAAGTC	54476
rs774088282	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672420	TGTTAAATTTAATAA[C/G]AAGAAGTGAAGCAAC	54476
rs774095781	snp	C/G/T	6.58994e-05	0.00573986	synonymous-codon	RNF216	GRCh38.p7	7:5641214	GGCTCCTGGTGAGCG[C/G/T]GGATGTTGGCAGAAA	54476
rs774134583	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5714008	AACATAAACTTTATT[G/T]ATTTATTTTTCTGAG	54476
rs774143115	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667111	GTGCCTGGCCAGCCA[C/T]GACTTTTAAACTATA	54476
rs774151766	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5757965	TTCAAGACCAGCCTT[G/T]CCAGGCAACATAGTG	54476
rs774165417	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5745133	AATATTAGCAAATGG[A/G]ATCCCCAGCAGCACA	54476
rs774176050	snp	G/T			intron-variant, downstream-variant-500B	RNF216, RNF216-IT1	GRCh38.p7	7:5662427	TACTTGTAAATACTT[G/T]CCACTTACCTCCTCA	54476
rs774176143	snp	C/G	1.65888e-05	0.00287996	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752902	GCTGCTGAGGAGCTG[C/G]GGTGACCAGCATTGG	54476
rs774186144	snp	A/T	1.71428e-05	0.00292765	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739328	CCTCAATAAACCCAT[A/T]TGCTACATCTGGAAA	54476
rs774190539	in-del	-/CT			intron-variant	RNF216	GRCh38.p7	7:5773692	CCTGCCTCAGCCTCC[-/CT]GAGTAGCTGGGACGA	54476
rs774191532	in-del	-/ATACATACAC			intron-variant	RNF216	GRCh38.p7	7:5748606	CAGTATATTTTTTAT[-/ATACATACAC]ACACACACACACACA	54476
rs774202034	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681035	CCTCCAGCCATACCC[C/T]GCAGATACCCCAGAC	54476
rs774213465	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5705444	TCAAATCTGCTCCTG[C/T]TCTCCAACTCCAAGG	54476
rs774223282	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5704646	TCCTCATGGAGCATC[A/T]GTGCCACCTAGTGGC	54476
rs774235345	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5729844	AAACCAATCTTACAG[C/G]CATCTTCTTTCCATA	54476
rs774237020	snp	C/T	1.64727e-05	0.00286986	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741619	CCAAGATCCAGAAAT[C/T]CACCGTAGTCATCCT	54476
rs774243305	snp	C/T	2.30934e-05	0.00339796	intron-variant	RNF216	GRCh38.p7	7:5739225	ATTTTTTATTACATA[C/T]ATTTTACCACCACCA	54476
rs774274552	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5696191	GTTGGTACCGCATGG[-/C]TTTAAATTGTTTGTA	54476
rs774280203	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5656456	GTATCGTGGCCATCG[C/T]GCGGGACCACACTTT	54476
rs774282580	in-del	-/AAAAA			intron-variant	RNF216	GRCh38.p7	7:5654686	GCCAGACTCCGCCTC[-/AAAAA]AAAAAAAAAAAAAAA	54476
rs774283041	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671362	TGGCTGTTATGAACT[A/G]AACTGTGTCTCCCTC	54476
rs774298290	snp	G/T	1.64727e-05	0.00286986	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741523	ACAATGTCATTTGCT[G/T]CTTGGTTATGACTCG	54476
rs774321644	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5649836	GATGTCATCTCTCAC[C/T]AGAACAAACAGCCCC	54476
rs774328665	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5704599	TTTTGCTGACACATA[C/G]TTTTCAAACACCCAA	54476
rs774333056	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5765045	CACTGCACTCCAGCC[C/T]AGGAAACAAAGCAAG	54476
rs774371322	snp	C/T	1.6696e-05	0.00288924	missense	RNF216	GRCh38.p7	7:5622895	GGGGGCCAAAGTGCA[C/T]GGGCAGGTTGTGCTC	54476
rs774409760	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5724263	ATGAAGGGACAACAG[C/T]CAGAATCTCTCTCCA	54476
rs774414486	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5756697	ATGAACACAAGTTCT[C/T]TGCAGCCTTGACCTA	54476
rs774419209	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5700180	GGAAGGCTGGAAACC[C/G]TGCAGTGCTCTGTGC	54476
rs774450331	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5762033	ACGCATAATAGAATA[C/T]ACGGACAGGGATGGT	54476
rs774457096	snp	A/T	1.65855e-05	0.00287967	missense, intron-variant	RNF216	GRCh38.p7	7:5741782	GGGCAGCTGGTTTGA[A/T]GAGATTGGGTCGTGA	54476
rs774457105	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664589	CCCAAGAGAACTTCT[A/G]GTTTAGAGGGGTCAG	54476
rs774460608	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665080	TGCGATTACAGGCAC[A/G]AACCACCGCACCCAG	54476
rs774463453	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5752383	TGGTTAGAAAGAGTA[A/G]TATCATAAAAATTGC	54476
rs774514057	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5735929	GGGAAACTGTCTCTA[C/G]TAAAAACACAAAAAT	54476
rs774521285	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5724742	ACAGAAAGGGATGAT[C/G]TCTAGAAAAGTTGTA	54476
rs774526605	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5708741	TGCTGTAAGCTGCCC[A/G]GCTCTTTTTTGGCCT	54476
rs774533742	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5755846	AAGCATATGCTCCAT[C/T]TTGGCAGATAACACT	54476
rs774551921	snp	A/C	1.64817e-05	0.00287064	missense	RNF216	GRCh38.p7	7:5725389	TTCTTCCTTTTTCCA[A/C]TGGTTTCTGGTGACA	54476
rs774577321	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5656491	CCCCTTGTGCCTTTC[C/T]GACTGGGGGAAACCA	54476
rs774603374	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5718462	GTTTTATAGTTTTTA[C/T]TTCAGAACTAAAATT	54476
rs774608848	snp	G/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682171	TCCCCTTTTCTAAAT[G/T]GCAAAGTTGGCAGAT	54476
rs774616993	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5699492	TCCCTGCTCAAGCTA[C/T]TCTTCCCATACTGGC	54476
rs774620008	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5747107	ACAGTCTACTAACTC[C/T]GAGTTGCCTTTCTTC	54476
rs774621414	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5748170	TGGCCTTACAAACAT[C/T]GTTTTCTGATGAACT	54476
rs774629026	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5623667	CCAACCTCCTGGGAT[A/C]CAGTGATGCTCCCAC	54476
rs774634750	snp	A/G	3.29538e-05	0.00405904	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741079	TGCATTGGAAAGGCT[A/G]GACCTGGCTCTTCAT	54476
rs774653312	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5626792	CTGCGTCCAGGAAGC[C/T]CATCTGTAAATGGGC	54476
rs774687563	snp	A/G	1.69026e-05	0.00290706	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5740999	CTAGTAGTTCAACGA[A/G]CTCTTGATCTACCTC	54476
rs774694407	snp	C/T	1.64787e-05	0.00287038	intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652402	TAGCCCCTCTGAATT[C/T]TGTTACTCACATAGA	54476
rs774702113	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5735186	GTTTGTGTAATCCAA[A/G]AACTTCAAGACAGGA	54476
rs774703066	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754826	TGAGGCCAGGAGTTC[A/G]AGACGAGCCTGGCCA	54476
rs774711224	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5717713	TCCCTATGAATTGCT[A/G]CAGAGTGACTGCCAG	54476
rs774738180	snp	C/T	1.65029e-05	0.00287248	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5729566	CAAGAGGGGTCAATT[C/T]AGAATAGTCAAAAAA	54476
rs774747712	snp	A/G	1.69043e-05	0.00290721	intron-variant	RNF216	GRCh38.p7	7:5715242	CACTTAAGGAGAGGG[A/G]GAGCCTTGTCTCCCA	54476
rs774753431	in-del	-/C	1.6476e-05	0.00287014	frameshift-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741089	AGGCTGGACCTGGCT[-/C]TTCATCATCACTTGC	54476
rs774795280	in-del	-/TCA			intron-variant	RNF216	GRCh38.p7	7:5743315	AAAAATGTATGTCTG[-/TCA]TCATTTTTTCATACT	54476
rs774795719	snp	A/G	1.6612e-05	0.00288196	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752897	TTCATGCTGCTGAGG[A/G]GCTGGGGTGACCAGC	54476
rs774802520	snp	C/T	1.65168e-05	0.00287369	missense	RNF216	GRCh38.p7	7:5715168	TCCCCATAGCAGCAG[C/T]GACACTCAATCAGCT	54476
rs774802705	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5706831	GGTATTATACCCAGG[-/A]AAATCATTGCCAAGA	54476
rs774806536	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5762916	TGGGGTAGTAGACTT[C/G]TATTTTTGTAATCCA	54476
rs774823145	snp	A/T			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622779	GATGCAATGGTACAG[A/T]CACCAGCCTTGGGGG	54476
rs774830197	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5623466	CAGTGACTCAGTTAC[-/T]TTTTTTTTTTTTTTT	54476
rs774847661	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5766382	GCCTCCAAATTCCTA[C/T]ATTGAAGCTCTGACC	54476
rs774848514	snp	C/T	3.30093e-05	0.00406246	synonymous-codon	RNF216	GRCh38.p7	7:5623046	AGGCAGGGGGAAGGG[C/T]GGGTGCGCGAAGGCA	54476
rs774877218	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5702074	GCCCCAGGTCGCTGC[C/T]GGGTTCTCGGAGCCC	54476
rs774884102	in-del	CCACTGCACTCCAGCCTGGGCAAAAAAAA/GCCTGGGCAAGAGTGAGACTATGTCTC			intron-variant	RNF216	GRCh38.p7	7:5725821	CACCACTGCACTGCA[lengthTooLong]AAAAAAAAAAGGAAT	54476
rs774884816	snp	A/C/T	3.57406e-05	0.00422721	intron-variant	RNF216	GRCh38.p7	7:5729634	AATCAGAGGCCAGGC[A/C/T]GTACATTTCCCATAC	54476
rs774902076	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5632916	CCCCAAATGCAGTGT[C/T]AAGGACAAAGGGTCA	54476
rs774907603	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5633950	GTCCACGCAGCAGGG[C/T]ATAGACAGGAGAAAA	54476
rs774907606	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5727714	AGCCTGGGTGAGAGA[A/G]AGAGACCCTGTTTCT	54476
rs774920795	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5637805	CTTGGGCTCTCGAAG[C/T]GCTGGGATTACAGGC	54476
rs774931083	snp	A/G			upstream-variant-2KB	RNF216	GRCh38.p7	7:5783585	CTTGATGCGGCAATG[A/G]GTGTTCCTTCTCTAA	54476
rs774942860	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5689111	ATATGGCACCACCAT[-/C]AGTGCCTTGTGAGCC	54476
rs774958435	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5658326	TAGTTCAAAAGATTC[C/T]TATTTTAATAAGCAC	54476
rs774960569	snp	C/G/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672750	CTGCTGTGGTCTTCC[C/G/T]GGTGAGCAGCGCAAG	54476
rs774974457	snp	G/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668012	TTGGTATTTTAGGGC[G/T]CTGTGTAAAGATGGC	54476
rs774981843	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5643301	GGTGACTACCTAGCC[A/T]GTAATATAAAAGTGA	54476
rs775006240	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5759774	GTAGCTGGGACTACA[C/G]GCATGCACCACCACG	54476
rs775018853	snp	C/G/T			upstream-variant-2KB	RNF216	GRCh38.p7	7:5782779	TGCTTGAACCGAGGA[C/G/T]GGGGAGGTTGTAGTG	54476
rs775047603	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5693442	TGTACTGAAATTGTT[C/T]CCTGCTGATGGGTAT	54476
rs775062583	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5777236	CGACCAGAGAAAAAT[A/G]GCCCAGGTGAGCACT	54476
rs775074992	in-del	-/CTT			intron-variant	RNF216	GRCh38.p7	7:5706487	CGTGCAGTATCTGTC[-/CTT]CTATGACTGGCTAAT	54476
rs775075695	snp	A/G			intron-variant, nc-transcript-variant	RNF216, MIR6874	GRCh38.p7	7:5711908	GTTCCAGCTCCATGT[A/G]GCTGTTCATATGAAG	54476
rs775083282	snp	G/T			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712664	AAGTGCCCAGGTAGT[G/T]TTCACAATGGGGAAG	54476
rs775152203	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5776050	CTTTGGATATCCATC[C/G]TTTTGTAAGTCTGTA	54476
rs775171551	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5765103	AGGATGGGATAAAAC[A/C]ATTTTTACACATTCA	54476
rs775182554	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5649467	TTAGCTGTGATTGTG[-/C]CATTGTATTCCAGCC	54476
rs775190492	snp	C/T	1.64977e-05	0.00287203	synonymous-codon	RNF216	GRCh38.p7	7:5721162	CATCCTCTTTTCTAT[C/T]TTTATGTCACCTAGA	54476
rs775219059	in-del	-/ACA			intron-variant	RNF216	GRCh38.p7	7:5630724	GCGCCAAGCACAGTG[-/ACA]ACAACAGTAGTTAAC	54476
rs775222357	snp	C/G	3.54868e-05	0.00421214	intron-variant	RNF216	GRCh38.p7	7:5730849	TGTTACTTTCATACT[C/G]CTTCCAAATCCCACA	54476
rs775224816	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682053	GCTGCCTCTTCTCAG[A/G]GTGGGGATGATGGAG	54476
rs775243459	snp	A/G	1.70003e-05	0.00291545	synonymous-codon, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712849	GCAGCTGCCTTCCAT[A/G]CAGCTGAGCTCCAAC	54476
rs775279062	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5750071	CTATTCATGAGTATT[C/T]TTATTTTTATGGCAA	54476
rs775279723	in-del	-/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665393	CTTAAATATTTTTTG[-/T]TTTCATACACACCTC	54476
rs775284690	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5745454	TCAACACTATTAAAA[C/T]TTTTGAGGAAGTACC	54476
rs775296467	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5746121	TTTTTTGGGAAGTAA[C/T]GTTTTCCTCATGGAG	54476
rs775297714	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5720750	ACATTTGATACTATA[C/T]TTAGAAAAATTAAAG	54476
rs775313215	snp	A/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672467	ACTACACACACATGA[A/T]GTAGTGCTTGTAGCA	54476
rs775325017	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673260	AGCATGGCCTCTCCC[C/T]GCCCACCTATCTACC	54476
rs775341572	snp	A/G	1.6477e-05	0.00287024	missense	RNF216	GRCh38.p7	7:5641197	GAACACTCCTGGCAA[A/G]GGGCTCCTGGTGAGC	54476
rs775361573	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5696392	TTTAAATGACTGGGA[A/T]AAAACTTGTGAAGGT	54476
rs775383603	snp	C/G	3.30087e-05	0.00406242	utr-variant-5-prime	RNF216	GRCh38.p7	7:5761116	CTAATATCTAAACAT[C/G]GTGACCATCTGTTTC	54476
rs775402489	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5626306	GGTTGGGTGGGCAGT[A/T]TGAAGGCCTCCATGT	54476
rs775421221	in-del	-/AAAAAAAAAAAA			intron-variant	RNF216	GRCh38.p7	7:5738089	ATAAGACTGTCTCCA[-/AAAAAAAAAAAA]AAAAAAAAAAAAAAA	54476
rs775456364	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5685151	CTCACTGGAGGCTCA[C/T]GGCCTCCAGTGATTG	54476
rs775498258	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5756939	CTGCGCCTGGCTGAG[C/G]TTTTTACTTCTTGTC	54476
rs775505541	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5779090	ATATAATGATATCAG[G/T]TATGAGAATGAATTA	54476
rs775521733	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665267	TTCCAAATGCAGAAA[C/T]TCAAATCTGGGAGTG	54476
rs775528039	snp	A/G	1.66588e-05	0.00288602	synonymous-codon	RNF216	GRCh38.p7	7:5641361	TCTAATGCGGGCAGC[A/G]GTCATTTTTTCTTCA	54476
rs775533608	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5770983	CGGCTAATTTTTGTA[C/T]TGTTAGTAGAGACAG	54476
rs775543042	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5691150	GTGTGTGTAGACGGT[A/G]AGCCTGGGTGATCAA	54476
rs775564991	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5701285	GGAGCTGGTAGAAAT[G/T]AGTTGAGTGGTGAGT	54476
rs775591179	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5630794	CACACCTCACATGGA[C/T]CTCAGTTTCACCACA	54476
rs775596856	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753249	AGGTTGGAGAAATCT[A/G]TTTACAAAATTTTCT	54476
rs775600884	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5631789	CAGAGATCAATCCTG[G/T]GAACATTCTGATATC	54476
rs775612685	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5645754	CGCCACCACATCCAG[C/T]TAATTTTTGTGTTTT	54476
rs775627543	snp	C/G			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681123	TCTTTGAACGCCTAG[C/G]CTCTTGCTTATAATT	54476
rs775628447	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5706727	TCAATTCCTTTCCAC[C/T]GGCTGCCTTTTCACT	54476
rs775662458	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5708410	GGGTGCACTGATGTC[A/G]GGTGCATATACAGAT	54476
rs775668314	in-del	-/AA	3.29772e-05	0.00406048	intron-variant	RNF216	GRCh38.p7	7:5652532	ATAAAGGACAGACAC[-/AA]AGACAACTCCTGGTG	54476
rs775675397	snp	A/G			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620538	AGGGTGGGTGCTCAC[A/G]GCAGCCCTGTGGTCC	54476
rs775680846	snp	A/G	1.64887e-05	0.00287125	intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652378	ATGGGGAAGTTGAGA[A/G]TCAGCCCATAGCCCC	54476
rs775691792	in-del	-/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682412	CTTTCATTTTTTTTC[-/T]TTTTTTTTTTTTTTT	54476
rs775706269	snp	A/G	5.08608e-05	0.0050426	synonymous-codon	RNF216	GRCh38.p7	7:5622881	GCGATGCCGCGGCTG[A/G]GGGCCAAAGTGCATG	54476
rs775707204	snp	C/T	0.000166987	0.00913594	intron-variant, splice-acceptor-variant	RNF216	GRCh38.p7	7:5739627	TTGAGCATCTCTGTC[C/T]AGACAAAGGGAATCC	54476
rs775733733	snp	C/G	6.69815e-05	0.00578673	intron-variant	RNF216	GRCh38.p7	7:5715226	CACATGAAATGTCCT[C/G]CACTTAAGGAGAGGG	54476
rs775734161	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5709510	TGACACTACCCCACA[A/C]CACATGCCTTTACGG	54476
rs775737202	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5701348	TCCACCTGCCCACTT[C/T]AGGGGAACTCCATGC	54476
rs775737556	snp	A/C/G			intron-variant	RNF216	GRCh38.p7	7:5690715	GCCCAGGGCTAGTGA[A/C/G]AGGTAGAGTGAAGAT	54476
rs775738826	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5715211	GGCAGTCAAGAAACA[C/T]ACATGAAATGTCCTG	54476
rs775756851	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5639563	CCGCCTCCTGGGTTC[A/G]AGCAATTCTTTCTCA	54476
rs775813441	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666536	CTGCCTGGGGCCTGA[C/G]CCCAGAGTAAACAGA	54476
rs775818567	in-del	-/G			intron-variant	RNF216	GRCh38.p7	7:5649399	AGGAAAAAAAAAAAA[-/G]ACAGAAAGAAAGGGA	54476
rs775823440	in-del	-/CTT			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780344	CTCTACGTCACAGTG[-/CTT]CTTCTGTAGGTGAAC	54476
rs775868369	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5748947	CCGTGTCTATATATG[C/T]GTTATGTGTGTGTGG	54476
rs775872934	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5638731	CAGCCTTGACCTCCC[A/G]GGCTCAAATGATCCT	54476
rs775931627	in-del	-/AATAAT			intron-variant	RNF216	GRCh38.p7	7:5737523	GAATGATCAATTAAA[-/AATAAT]AATAATAATAATAAT	54476
rs775946237	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673843	ATAGAGAGACCTCCA[C/T]CTCTCTCTTTCTCTC	54476
rs775947758	snp	C/G	1.64727e-05	0.00286986	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741250	CCCAGTTCTGCTTCA[C/G]GCTGCCGTTCCTGAG	54476
rs775952867	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5737549	TAATAATAATAATAA[-/A]TAAATAAATATAAAT	54476
rs775961689	in-del	-/G			intron-variant	RNF216	GRCh38.p7	7:5655628	GGGGGGACAAAAAAA[-/G]ACAAGACCAGACCAT	54476
rs775969387	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5766544	CATCATGTGAGAACA[C/T]AGGGAGAAGGCAGTT	54476
rs775976676	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5756916	GCTGGCATTACAAGC[A/G]TGAGCCACTGCGCCT	54476
rs775980474	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5649577	CCCAGAGGGGCTATA[C/T]GATAAGGAAAGGCAA	54476
rs775991294	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5629019	TGTGGCTAACACGGT[A/G]AAACCCCATCTCTAC	54476
rs775996179	snp	G/T	1.64966e-05	0.00287194	intron-variant	RNF216	GRCh38.p7	7:5652545	ACAAAGACAACTCCT[G/T]GTGAGTGGACACCAC	54476
rs775997451	snp	G/T	1.67089e-05	0.00289035	missense	RNF216	GRCh38.p7	7:5623089	TGTGGCTGTGGCAGG[G/T]TCTGCGGAACGGGCC	54476
rs775999162	snp	C/G	1.6473e-05	0.00286988	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741182	TCCCACCTTGCTGGG[C/G]TTCCGGCCTTGGAAA	54476
rs776010018	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5693611	CAAGCTACAACCTCC[C/G]CAAGTGTCAATTCCT	54476
rs776013995	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5694394	ATGAGCTCAGAATCT[A/G]TTCTGACCACGAGCA	54476
rs776043759	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678189	TTACTTCTGAGGCTC[C/T]GGGGCCCTCTGCTGA	54476
rs776046717	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5718679	CCTCATCCTCCCAAG[C/T]AGCTGGGATTACAGG	54476
rs776100872	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5684576	TGCTGGAAATCAAGT[C/T]TGGCTGATGTCAGGG	54476
rs776128890	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5627188	CTTGTTCAATGTTAC[A/G]GCTAGTTGGCGGTAA	54476
rs776129537	in-del	-/GGATG			intron-variant	RNF216	GRCh38.p7	7:5638028	CGCAGCAGCCCCCTT[-/GGATG]GGCCCCACACCCTCT	54476
rs776134453	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5708849	CAGCCCCTTGAGAAG[C/T]CCAAATGCTGAACAC	54476
rs776143046	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672822	TAGAGCACTGGGAGG[C/T]GAGGAGCTGGGGCTT	54476
rs776157397	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5645598	GTTTCTTAATTTTTC[-/T]TTTTTTTTTTTGCAA	54476
rs776201406	snp	C/G/T			intron-variant	RNF216	GRCh38.p7	7:5725147	AAGGAAGCCAACAAG[C/G/T]GCAGCCACTTCCTAA	54476
rs776208223	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5704307	GAATTTATATTACTG[A/G]CAAAGACACTGCAAT	54476
rs776211172	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5763206	TTAAGTGACATGAGG[A/G]AACCTTTCCGGGTTA	54476
rs776283721	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678803	CGGAGCAGATTTCTC[A/G]ACTCCACTTCATCAG	54476
rs776295419	in-del	-/ACTT			intron-variant	RNF216	GRCh38.p7	7:5690850	CCACACCAGCCTGAC[-/ACTT]AATAACACATACGCA	54476
rs776297236	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664832	TGAAGTTTTGCTCTT[A/G]TTGCCCAGGCTGGAG	54476
rs776312395	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5710367	CTGCCTCAAAACTTA[-/A]AAAACAAAAACAAAA	54476
rs776314912	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5690702	GGCAGTGGGAAGTGC[C/T]CAGGGCTAGTGAGAG	54476
rs776316836	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5714216	TCCACCCAACTTAGC[A/C]TCCCAAAGTGCTGGG	54476
rs776322001	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5634496	CCCAGCAACAGGAAG[G/T]TGGGGGAGGGAGCAG	54476
rs776328031	snp	A/C	1.65021e-05	0.00287241	intron-variant	RNF216	GRCh38.p7	7:5716787	GAACAAAAAAGGCAC[A/C]CATTCAGACACAAAT	54476
rs776355060	snp	A/G/T	8.23681e-05	0.00641702	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741349	CAGTCTTCTTCGATG[A/G/T]CCTGATCATCTGCTA	54476
rs776373223	in-del	-/G			intron-variant	RNF216	GRCh38.p7	7:5690674	ACAGAAGAGCAAACA[-/G]GAAGTCCACAAAGGC	54476
rs776374692	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5627892	AGCATGCAGGCCACT[A/G]CCTGATTTTTATCAC	54476
rs776379339	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5778057	GCCTTGCAGGCTCCA[G/T]CCCTTGACATGTTTT	54476
rs776382188	snp	C/T	1.91261e-05	0.00309236	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5730731	TTTGTCTCATCTTGG[C/T]TGGCCAGCAGACTGC	54476
rs776393751	snp	C/T	1.72826e-05	0.00293956	missense	RNF216	GRCh38.p7	7:5624086	TCTGTTCCTCTTCAG[C/T]CTCCTTCTGGATTTC	54476
rs776396037	snp	C/T	1.64811e-05	0.00287059	synonymous-codon	RNF216	GRCh38.p7	7:5725376	CATTTGTTTTCTCTT[C/T]TTCCTTTTTCCACTG	54476
rs776399703	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5771891	GCAAAAGGCCAATAA[A/G]TAAATGAAAAAGTGT	54476
rs776407735	in-del	-/GA			intron-variant	RNF216	GRCh38.p7	7:5756051	ATCCCCACAAGTCAC[-/GA]GCGGGACAGGTGGAG	54476
rs776412443	snp	A/G	1.648e-05	0.0028705	intron-variant	RNF216	GRCh38.p7	7:5760957	AGCTGTGATACTAAA[A/G]GAAAAAGCCACAGGG	54476
rs776415157	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5742096	CTGCTACCCAGGCTG[C/G]AGTGCAATGGTGCGA	54476
rs776416384	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5733368	GTACACGTGTGAGAC[A/T]CAGGAAGTAGGAGAA	54476
rs776423846	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5735012	AAAAACTAGCTGGGC[A/G]GTGGGCACCTGTAAT	54476
rs776434588	snp	G/T			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712090	TCCCAACCTTAATGA[G/T]AACTCCTTGCATATA	54476
rs776447106	snp	A/C/T	5.10559e-05	0.0050523	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5740996	TCACTAGTAGTTCAA[A/C/T]GAGCTCTTGATCTAC	54476
rs776454316	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664296	TATACGACCCTTTCA[A/G]GTTAATTCATTACAG	54476
rs776461079	snp	C/T	1.65762e-05	0.00287886	synonymous-codon, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712780	CTCATAGTACTTATA[C/T]AGGATGGTCTGGGGG	54476
rs776467376	snp	A/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663348	CACTTTGGGAGGCCG[A/T]GGCAGGTGGATCATG	54476
rs776480814	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679410	GCCTCACAAGGGGCT[A/G]GGTTGTGAGGATGCA	54476
rs776503329	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5730413	TGGCCAATTCTTGTT[C/T]TGCTTTAGGAATTTG	54476
rs776514174	snp	C/T	1.65034e-05	0.00287253	intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712697	TTGGCAGATGGCACG[C/T]TCTGCCTGAGAACGA	54476
rs776520878	in-del	-/C	1.65562e-05	0.00287712	frameshift-variant, intron-variant	RNF216	GRCh38.p7	7:5741773	CTTGCCACTGGGCAG[-/C]TGGTTTGATGAGATT	54476
rs776545880	in-del	-/GC			intron-variant	RNF216	GRCh38.p7	7:5625067	ACCCGCCAAGTGGGT[-/GC]GCCCATCTTTCCTGG	54476
rs776547253	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5653710	TGAAGGAAAACATAG[A/T]GTTGTCAGTTTTAAG	54476
rs776566844	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5626757	TTAGCTAAGTGAGCT[C/T]GGCAGGTTCCTGAGT	54476
rs776597824	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669283	TTTGATCCAGGTCTT[C/G]GTTTTGCTGATCCTC	54476
rs776610420	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5746357	TGCTCCCTCTTTGCA[G/T]AGGTCTTTACGGCTT	54476
rs776643083	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5648238	CAGCCTCCTGAGTAG[C/T]TGGCATTACAGGCAT	54476
rs776647258	snp	A/G	0.000934714	0.0215982	intron-variant	RNF216	GRCh38.p7	7:5725301	TTGCAGCTACACACT[A/G]CCACCAACACAGTTT	54476
rs776665537	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5691383	GCTGGATTGCTCCTG[C/G]CTGGATTGCTCCAGG	54476
rs776665586	snp	C/G	4.95823e-05	0.00497882	missense	RNF216	GRCh38.p7	7:5715079	CAAAGACTGCCTCTT[C/G]GGCATATCTGATGAG	54476
rs776691410	snp	A/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672599	ACATGTTGAATTACA[A/T]TTTTATCCACTTACA	54476
rs776704459	snp	A/G			utr-variant-3-prime	RNF216	GRCh38.p7	7:5621567	GGCCCTGCTTCAGGA[A/G]GTGGCGGGCCACTCC	54476
rs776704904	snp	G/T			intron-variant, splice-acceptor-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662567	AGACAGTTTCTGCAC[G/T]GAAAGGAATGAAGAC	54476
rs776719567	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5745494	TTAGACACGTGAAAG[A/C]AGCATAAAAATTGGA	54476
rs776720783	snp	G/T	1.64735e-05	0.00286993	missense	RNF216	GRCh38.p7	7:5729465	GTGTCCTTTGAGCTC[G/T]TGCAGGGCCCACTTG	54476
rs776771040	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5771135	ATATGAATGTTTATG[A/G]CAAAAGTAGCATTGC	54476
rs776771165	snp	A/G			upstream-variant-2KB	RNF216	GRCh38.p7	7:5782500	CAAGGCAGGAGGATC[A/G]CTTGAGGCCAGGAGT	54476
rs776784552	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780558	AAAAATTAGCTGGAC[A/G]TGGTGGCAAATGCCT	54476
rs776800966	snp	C/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754730	TCTTGGTGTACCCAA[C/T]GAAAAAGTTGGTTTA	54476
rs776806292	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5749611	GTTTTTAACCACAGC[C/G]ATTTTAAGTCTTGCT	54476
rs776809455	snp	C/T	1.64947e-05	0.00287177	missense	RNF216	GRCh38.p7	7:5715138	GCGCACTGCGTCAGC[C/T]CCTCGAATGGAAATT	54476
rs776852107	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677506	CATATCGAAAGGCCA[C/T]TTATATGGCTTCTGG	54476
rs776863547	snp	C/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5780857	CGCACGCCGCGCACG[C/T]TCCAGGGTTGGTTGC	54476
rs776887119	snp	C/G	1.64746e-05	0.00287002	missense	RNF216	GRCh38.p7	7:5641232	ATGTTGGCAGAAATG[C/G]TCATATCCATTAATA	54476
rs776890352	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5682128	GCCATGCGGGCCCAC[A/G]CTGCTAGGAAAAACC	54476
rs776902379	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5740455	AATATCACCACTAAT[A/T]GAACTTTGTTGGATG	54476
rs776919008	snp	C/G	3.73232e-05	0.00431975	intron-variant	RNF216	GRCh38.p7	7:5739262	CCACAAAAAAAGCAT[C/G]GTAGTATACTTACAC	54476
rs776934361	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5656754	CCGTCTTCCTTTATT[C/T]ATTTTCTGCTGCCTG	54476
rs776935208	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5640841	GGCTTTGGAATCAGC[A/G]TTATGCTGGCTTTGA	54476
rs776950279	in-del	-/AT			intron-variant	RNF216	GRCh38.p7	7:5749921	CTGCTGGTTCTTTTA[-/AT]GTTTTGTTTTCCAGA	54476
rs776952350	in-del	-/TCAA			intron-variant, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711345	AAGATGCCCAGTTCC[-/TCAA]TCAAAGAAGCGTCGT	54476
rs776975735	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5716433	CTCGTTAACTCTAAA[C/G]TGATATCTAAGTTGT	54476
rs776997402	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5765195	GACCGGGCATGGTGG[C/T]TCACGCCTTTAATCC	54476
rs777015085	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5740362	TGATATCCTGATCTT[A/G]TGATCCACCCACCTT	54476
rs777020537	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5727392	GAGTGGCCAAGTCTA[C/T]AAGTCTACCATCTAC	54476
rs777034682	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5773985	AATGTCAGGCTTGTA[G/T]TTAAGCAGACTGCTA	54476
rs777037835	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5774893	CTCCCAAGTTACAGG[C/T]ATGTTGCCACCATGC	54476
rs777046723	in-del	-/A			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712472	GCGAGAATCCACCTC[-/A]AAAAAAAAAAAAAGA	54476
rs777092689	snp	C/T	1.66696e-05	0.00288696	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752889	TCCTCTTCTTCATGC[C/T]GCTGAGGAGCTGGGG	54476
rs777098396	snp	G/T	3.29995e-05	0.00406185	missense	RNF216	GRCh38.p7	7:5623038	CGCACGGGAGGCAGG[G/T]GGAAGGGTGGGTGCG	54476
rs777125231	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5650987	AAGTCACCCAACTAC[A/G]GGCTACATACGGTGC	54476
rs777170690	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5745689	TGGATAACTTGAGGT[C/G]AAGAGTTAGAGACCA	54476
rs777173855	snp	C/T			downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620022	TAACTTGCCGGATGG[C/T]GGGGTGGAGAGACGA	54476
rs777190926	in-del	-/G	0.000296711	0.0121765	intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652389	GAGAATCAGCCCATA[-/G]CCCCTCTGAATTCTG	54476
rs777191881	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5764419	CTGGGAGGCTGAGGA[C/G]AGCGGATCACTTGAA	54476
rs777201071	snp	A/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754464	GCCACCATGCCTGAC[A/T]TAATTGTGGATTTTT	54476
rs777205444	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672924	GACCAAGGGGGATGT[C/G]TTGAAATTGGAAAAT	54476
rs777210941	snp	A/G			intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5780048	CTATTGCAGGAAGAT[A/G]GAGGACAAACAACAG	54476
rs777238871	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5772703	TACTATCAAAATATA[C/G]AGATATCAAAACCAG	54476
rs777242850	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5709608	AAGTTCAGCAGGCCA[C/T]GTATATTCCTCCCAT	54476
rs777244960	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5720449	TACCAAACGTGCTCA[G/T]CGACTATTATGGGTA	54476
rs777258789	snp	A/G			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5621026	AGCAAAGTTCAGGCA[A/G]TCCAACAGGTATGGG	54476
rs777283895	snp	C/T	1.64741e-05	0.00286998	missense	RNF216	GRCh38.p7	7:5721053	CCATCTCTTTGATTT[C/T]CTGCTCATAGAACTC	54476
rs777294181	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5646284	TGAGGCATGAGAATC[A/G]CTTGGGCCCAGAGGT	54476
rs777302460	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672142	GATCTTCTTCATACA[C/T]GTTGGAGACGTTAAG	54476
rs777307401	snp	A/C	1.67553e-05	0.00289437	missense, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712828	ACTGGTTGGGAACGA[A/C]CACGTGCAGCTGCCT	54476
rs777334833	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5710613	ATCTCTCCCCACCTC[A/G]GGACAGTGTGCTGCA	54476
rs777367744	in-del	-/TA			intron-variant	RNF216	GRCh38.p7	7:5649572	TGGTCCCAGAGGGGC[-/TA]TATATGATAAGGAAA	54476
rs777384482	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5682518	GTTCAAGCGATTCTC[C/T]TGCCTCAGCCACCCG	54476
rs777388149	snp	A/C/G			intron-variant	RNF216	GRCh38.p7	7:5636570	CAGGCTTGTGTGACA[A/C/G]TGCATGCTTTGTTTC	54476
rs777396891	snp	C/T			intron-variant, downstream-variant-500B	RNF216, RNF216-IT1	GRCh38.p7	7:5662305	CAGTTGCATGTCTGG[C/T]GGTATAGCAAAAGGA	54476
rs777401363	snp	C/T	1.64857e-05	0.00287099	utr-variant-5-prime	RNF216	GRCh38.p7	7:5761093	GCAGACATGCATATA[C/T]GGGACTGCTAATATC	54476
rs777420192	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5657140	TCCCTTACTTTTAAA[A/T]GGTTCCTACAGTGAA	54476
rs777420230	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5707038	CAGAGACTACCTTTT[-/C]CCCCCGGTGGGTGTT	54476
rs777428996	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5701206	CTGTCATTTCTTATA[A/G]AATGTATCAGTTAGC	54476
rs777442113	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5723921	ATTAAACTACTAATG[C/T]AAATCAAGTGTAATT	54476
rs777447998	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5631680	ACATAAAAAAAAAAA[A/T]GCCATTATTTCTTTT	54476
rs777450811	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5725148	AGGAAGCCAACAAGT[A/G]CAGCCACTTCCTAAA	54476
rs777478719	snp	C/T	3.42149e-05	0.00413598	missense, intron-variant	RNF216	GRCh38.p7	7:5741812	ATCTCTGAGGTTTAT[C/T]TGTCTAAGAAAAAAT	54476
rs777481711	snp	C/T	1.64735e-05	0.00286993	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741393	TCCTAGATTTGATAA[C/T]AGCTCTGTCTCTGAG	54476
rs777496548	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5763100	GGAAATGGACTCATA[G/T]GAGAGTAATGGGGAC	54476
rs777504998	in-del	GAGATGGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTG/TTTAGGGGGTTCCCCCTTTCCCCCCCGCCGGGGT			intron-variant	RNF216	GRCh38.p7	7:5684121	TTTTTTTTTTTTTTT[lengthTooLong]GCGTGATCTTGGCTC	54476
rs777528693	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5718799	TGATCTGCCCACCTC[A/G]GCCTTCCAAAGCATG	54476
rs777532869	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5651311	GGCTCACTGCAACCT[C/G]TGCCTCCCTGGTTCA	54476
rs777539320	snp	A/G	1.64773e-05	0.00287026	missense	RNF216	GRCh38.p7	7:5761012	ACTTACCTTGTCCCC[A/G]ATGGCAGTGAAAGTT	54476
rs777540795	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5716046	GCATCCAGCCCCATT[C/G]TTTTATTTATTTATT	54476
rs777554882	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5630379	AGAAGCCAATCATCT[C/T]GTACCTTTTTTTTTC	54476
rs777564331	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5706765	TGGTTTCCTTTGCTG[-/A]AAGCATCTTAGTAGT	54476
rs777568305	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5726750	TGTAATCCCAGCTAC[C/T]TGGGGGGCTAAGGCA	54476
rs777576980	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5773694	TGCCTCAGCCTCCCT[A/G]AGTAGCTGGGACGAC	54476
rs777593520	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5632106	ATGGCTCAGGCTGGG[-/T]TGCTGGGCTCACCCT	54476
rs777607198	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5656401	CATTTTGGAAGGCAA[A/C]GTACACTTTGACGAG	54476
rs777615094	snp	G/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667340	AAAGTTTAAAAGCCA[G/T]TAATTTAGAATTCAT	54476
rs777620100	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5709939	TTTAAAATTTTTTTT[A/G]TAGAGATAGGGTCTA	54476
rs777624826	snp	C/T	3.2975e-05	0.00406035	synonymous-codon	RNF216	GRCh38.p7	7:5622989	CGGGGCTGGGATAGG[C/T]CCCATGTTGAGTGGG	54476
rs777641472	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5640372	CAGCGTAGTAGCTAG[C/T]GTGACCTGGGAAACA	54476
rs777644716	snp	C/T			utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620456	CTTCTCTCCCCAATG[C/T]TGTCACTGGTCCAGG	54476
rs777669971	snp	A/C	0.000167062	0.009138	intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753019	TACTGGGAGGTTGGC[A/C]CTATCACATCCAACT	54476
rs777676348	snp	A/G	1.65149e-05	0.00287353	synonymous-codon	RNF216	GRCh38.p7	7:5622932	CATGTGGATGGGACC[A/G]AAGTCATAGTTGACC	54476
rs777679052	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5695005	AGTTAAGGCTTCTGT[C/G]GCTCAACTTTAACTG	54476
rs777688256	in-del	-/AAATAAAT			intron-variant	RNF216	GRCh38.p7	7:5734826	CAAAACTCTCTCTCA[-/AAATAAAT]AAATAAATAAATAAA	54476
rs777708022	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5685196	AATGTCCACCACGGA[C/T]GGGTGGGCATGGAGG	54476
rs777708104	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5685786	AGAGCTTTAAATATT[C/T]AAAGCCCCATTAATC	54476
rs777709062	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5690438	CTGACTGCTTTGTTA[A/G]GGTTTCCCAGGTAGT	54476
rs777726778	snp	C/T	4.95741e-05	0.00497841	synonymous-codon, intron-variant	RNF216	GRCh38.p7	7:5741747	CCTTTCTTCTCCCAA[C/T]CTTTTCAGATCTTGC	54476
rs777726854	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5709340	CATGGTGCTGTGCCA[A/G]GGGGAGGAACTCTGG	54476
rs777729192	snp	A/G	1.72525e-05	0.002937	missense	RNF216	GRCh38.p7	7:5622874	ATCAGAAGCGATGCC[A/G]CGGCTGGGGGCCAAA	54476
rs777743803	snp	C/T	3.295e-05	0.00405881	missense	RNF216	GRCh38.p7	7:5652497	CAGAGTCCCTGACAC[C/T]TCCTACAGGTTTCCT	54476
rs777755663	snp	A/G			intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739408	GAATGGTTTCAAATG[A/G]CAATACAAGACAGAT	54476
rs777762944	snp	A/C/G	9.88344e-05	0.00702912	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741231	ATGCTGAAACAACAA[A/C/G]CGGCCCAGTTCTGCT	54476
rs777774277	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5657236	CAATCCAGAAGTAGC[C/T]TCAGAAATTTCAGCT	54476
rs777795346	snp	C/T	1.70574e-05	0.00292035	missense	RNF216	GRCh38.p7	7:5623116	GGCCTCGGGAGGGCC[C/T]CCACCCTCTGCACCT	54476
rs777796093	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676302	GACCACCGCGGCCAG[C/T]CTCAAGTTCTTTCCA	54476
rs777798857	snp	C/G/T	6.59593e-05	0.00574248	intron-variant, downstream-variant-500B	RNF216	GRCh38.p7	7:5652371	CAGGTTAATGGGGAA[C/G/T]TTGAGAATCAGCCCA	54476
rs777818550	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5700131	GTGTTTTCATGCTTG[C/T]GGTATTACCATAGCA	54476
rs777820147	snp	A/G	3.30164e-05	0.00406289	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752946	TCTGAGGAGTCAGAT[A/G]TGGTGATGGGCCCAT	54476
rs777834402	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5743673	ATATACACATGGATA[C/T]ATACAAATTCAAAGA	54476
rs777835645	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5639352	GAGCTGCTAGCCCAC[A/C]CCTGGGCTGTTCATC	54476
rs777841579	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5758089	TATACATACTCGTCT[A/C]ACAAAATATATCTCC	54476
rs777844358	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5719339	CATGATTGCATCACT[A/G]CACTCCAGCCTAAGT	54476
rs777856851	snp	C/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767238	TTCAGGGGCTCTGAT[C/G]CATGAAAAATGAGAA	54476
rs777859989	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5756383	TGGTATAGCTGAATA[C/G]TTGCAACAGAAACCA	54476
rs777866534	snp	C/G	1.65225e-05	0.00287419	missense	RNF216	GRCh38.p7	7:5623066	GCGCGAAGGCATAGG[C/G]TGGCATCTGTGGCTG	54476
rs777885019	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5626161	TCCAGGGTTAACACA[C/T]AAGAATTCTCTATCA	54476
rs777886744	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5647101	GGCTGTTTCAGCCCT[C/G]AGGAAGTTGTGAAAG	54476
rs777902188	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5724526	TAGTTCTACATTCTG[C/T]CACAGGCCAGGGCGA	54476
rs777940856	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5729055	TGTTCCCGGACTCTC[C/T]ACAGACCTTACGTCC	54476
rs777942401	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5757482	TTTTTTAAATCTTTA[C/T]TTTACCTTCATTTTT	54476
rs777956050	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5649284	GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	54476
rs777967278	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5634307	CCCTCTGAGATTCTG[A/G]GGGTGGGTTGGGGCT	54476
rs777982496	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5769142	TTTTTTTTTTTTGAC[A/G]GAGTTCCCCTCTGTT	54476
rs777986907	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5695128	TGACTTCAAGCTACA[A/C]GAAGTTAGCACTTAA	54476
rs777995180	snp	A/G	3.29489e-05	0.00405874	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5729545	CTTGGATGAAGCAGC[A/G]CTGGTCAAGAGGGGT	54476
rs777996035	in-del	-/GA			intron-variant	RNF216	GRCh38.p7	7:5682533	CTGCCTCAGCCACCC[-/GA]GTAGCTGGGACTACA	54476
rs778006798	snp	C/T			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680703	CACCGCGCCCAGCAC[C/T]CAACACTTCTACTTG	54476
rs778013843	snp	C/T	3.29457e-05	0.00405854	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741167	AAGAGGGGCCTGAAA[C/T]CCCACCTTGCTGGGG	54476
rs778026989	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5718317	ACCCAGGAGTCAGAC[A/G]TTGCAGTGAGCCGAG	54476
rs778030776	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5747654	TACTCTGGAGGCTGA[C/G]GCACAAGAATCACTA	54476
rs778035430	snp	A/G			synonymous-codon	RNF216	GRCh38.p7	7:5729441	GAGTACCTTTCGGGT[A/G]ATTGCATAGTGTCCT	54476
rs778045741	in-del	-/ATTA	1.8368e-05	0.00303046	intron-variant	RNF216	GRCh38.p7	7:5623213	TTAGTGGAGAAAAAC[-/ATTA]AACCAACCTCAATGG	54476
rs778078684	snp	A/G	1.65217e-05	0.00287412	synonymous-codon	RNF216	GRCh38.p7	7:5641157	GTGTCTACTTACAGT[A/G]GGATCGGTCCAGAGA	54476
rs778092238	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5704053	ACTAATGAATTCTTT[A/G]TCTGAGAACACACAA	54476
rs778109278	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5628545	TCCTTTTCTTTGAGA[C/T]AGTGTCTTGCTCTGC	54476
rs778113373	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5721918	TTGTTTCACTGATTT[C/G]GCAATTTATGATTTT	54476
rs778114618	snp	A/G/T			intron-variant	RNF216	GRCh38.p7	7:5655837	TCAGCAAATGCTTAC[A/G/T]CATATTACGAAGAAA	54476
rs778120915	in-del	-/TGTA			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674503	GTGGTGGCACACACC[-/TGTA]TGTAGTCCCAGCTAA	54476
rs778132195	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5750711	CAACAGCAAACCACA[C/T]TGGAGCAAGACTCCC	54476
rs778136330	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5751392	AAGTGTGTGCACTAG[A/G]CCCCAAAAGACCAGA	54476
rs778156035	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5633824	TGCTGCACTTGAAGA[C/T]GGCAAGTGAGGTAGA	54476
rs778162981	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5654227	GAGGAAGTAAGACTG[C/G]TGGGTGTAGAGATGA	54476
rs778182105	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5694094	GCCAAGGAAATTATA[C/T]CACTTAGCTCTTTGA	54476
rs778183712	snp	C/T	1.64784e-05	0.00287035	missense	RNF216	GRCh38.p7	7:5721124	TAGGACCTACAATGT[C/T]GTCGCTTATTTTCAA	54476
rs778184662	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5688058	CTAGCGACCGCAAAT[A/G]GAACCGAAGAGGTAA	54476
rs778200888	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5777949	GTAAGTACATCCTCA[C/T]GTGTGGAGGGTAAAA	54476
rs778221501	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5645015	TTTTTAGGCGTTTCA[A/T]CATATTGGCCAGGGT	54476
rs778248725	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5643595	CATATTCTGATGGTG[A/G]CATAAGCCATGCCCT	54476
rs778256881	snp	G/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669599	TATCACTGTTGAAAC[G/T]GAGACTGTGTTGGCC	54476
rs778272977	snp	C/G	1.65184e-05	0.00287384	missense	RNF216	GRCh38.p7	7:5725431	TTTTTAATGGCATCA[C/G]ACAAGGCCTAAAAAT	54476
rs778274655	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678605	TCCCTATCTATAAAA[A/G]GAGTGCTTATAAGGA	54476
rs778283137	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5737644	TGTCATTGTACAAAT[C/T]AGAAAAAAGTACCTA	54476
rs778284628	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5688856	AATTCCCAAATGATG[A/G]TAACAGCTACTAACA	54476
rs778290382	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5702745	TTTAAAAAGTGAAAT[C/T]TTAAAAAGTGAAAAC	54476
rs778303202	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5733262	TTCCCTTGCTTTTTG[C/G]ATTTCACGAGAATTT	54476
rs778321071	snp	A/C	1.9482e-05	0.00312099	intron-variant	RNF216	GRCh38.p7	7:5739251	CACCACCACCACCAC[A/C]AAAAAAGCATGGTAG	54476
rs778327565	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5746634	CTTGGAGCCAACGTC[A/T]TCCCGGTCCTGAGAT	54476
rs778352880	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5651734	GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAA	54476
rs778373011	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5682638	TCTTGAACTCCTGAC[C/G]TCAAATGATCCACCC	54476
rs778374326	snp	C/T	1.64727e-05	0.00286986	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741565	GGTTCTCTTTCTGTT[C/T]GGCCACTTGGCTTAG	54476
rs778393807	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5706454	CTGACTACTTTAGAT[C/T]CTGCATTTAAGTGGA	54476
rs778404252	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5722839	CCAACCTGTCCAACA[C/T]GGTGAAACCCCCCAG	54476
rs778413785	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5636655	GAATTCGATCGGTCT[C/T]CTGGTGAGAATCAAG	54476
rs778415011	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5760755	TAAGACTCAATGACT[A/G]CATATTAACAGCGTC	54476
rs778420419	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5637404	AGCTTTGTAATCTGA[A/G]TGATTTTTAGGGGTC	54476
rs778420491	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5732964	TAACCAGCCAAAGTA[C/G]ATTACCTGCCATGTG	54476
rs778421046	in-del	-/TTTTTTTTTTTTTTTTTTTTTTTT			intron-variant	RNF216	GRCh38.p7	7:5740107	CCAGATGTAACACCT[-/TTTTTTTTTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTGT	54476
rs778427445	snp	C/G	6.58903e-05	0.00573941	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741461	TTTCTGTGTAAAGAA[C/G]GCTACCTTCTTCCAA	54476
rs778460753	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5671319	CCCAACTGAATCACA[C/T]GTGCTAAAAAGACAC	54476
rs778471742	snp	C/T	1.65326e-05	0.00287507	missense, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5712754	GCCGCAACCTCCTCC[C/T]CGGCTTTTCGCTCAT	54476
rs778483882	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5697008	CAGGGACGGGGGTAG[C/G]GGAAGTCTCCAAAAT	54476
rs778491862	snp	C/T	8.80181e-05	0.00663335	missense	RNF216	GRCh38.p7	7:5622867	CGGGGCCATCAGAAG[C/T]GATGCCGCGGCTGGG	54476
rs778492488	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5776416	GTGAAACCCCGTCTC[G/T]ACTTAAAAAAAAAAA	54476
rs778504347	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5627510	CCCAGCACTTTGGGA[A/G]GCTGAGGCAGGCGGA	54476
rs778522032	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5746043	GGTCTGGCAACCCAA[A/G]GGGACAGAGACTGTT	54476
rs778522040	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5647800	TTTCTTAAATTTATC[C/T]CCTCTTCTCCATTTA	54476
rs778525036	snp	C/T	3.29739e-05	0.00406028	missense	RNF216	GRCh38.p7	7:5725359	ATGTAAGAATACTGG[C/T]TCATTTGTTTTCTCT	54476
rs778538425	snp	A/T	0.000136398	0.00825713	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739530	CATCTGTCTACATAG[A/T]AGATGAGGTCTAGAA	54476
rs778547772	snp	A/C			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662977	CCAGCACCCACACCC[A/C]CTATGCCCTCAATGG	54476
rs778558506	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5652990	TTGGGTTTTTAAAAC[-/A]ACAGTAGCACGAGCT	54476
rs778559130	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5691889	CCCACTTAATGCTTT[C/T]ACAGCGGAAGTCAAG	54476
rs778588985	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5720733	CATTCCAGCTGACTT[C/G]CACATTTGATACTAT	54476
rs778598081	snp	C/G			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622235	AGTTAGGCGGCAACA[C/G]AACAAAACCCCCGCC	54476
rs778616945	snp	A/C			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679049	AAGTTGTAAAATTTA[A/C]GAGTACAGAGATTAG	54476
rs778624283	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753920	GAATCGTTTGAACTC[A/G]GGAGGCAGAGGTTGC	54476
rs778627832	snp	A/C	0.000205276	0.010129	intron-variant	RNF216	GRCh38.p7	7:5760464	GAGCTCGTGGTGAGT[A/C]GAGATTACGCCATTG	54476
rs778633218	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5769095	GGTAAAATAGTTTAT[C/T]AGACACAATTTACAG	54476
rs778634148	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5657252	TCAGAAATTTCAGCT[A/C]TCTGTTCTGTCACCT	54476
rs778637618	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664045	CACCGTACATCTCAG[C/G]TATCTTTGGATTTCT	54476
rs778651038	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5740161	AGATAGAGTCTCACT[C/G]TGTCGCCCAGGCTGG	54476
rs778676390	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5707480	ATGTGCTAATTTTGT[A/G]TCCTGCACCTTTACT	54476
rs778695260	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5703022	CTGCGGCCTGAACCT[A/G]AAGCTCTTCAGAGGG	54476
rs778708975	snp	A/T					GRCh38.p7	7:5621067	GACATAGCAGCAGGC[A/T]GCCCCCAAGCCCGGC	54476
rs778722026	snp	A/G					GRCh38.p7	7:5657768	ATACAGAAGGCCAGA[A/G]AGACACTGATTTTAA	54476
rs778754361	snp	C/T					GRCh38.p7	7:5771715	GGTGGGAAGATCTCT[C/T]GAGCTCGAGAGGTGG	54476
rs778775273	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5701288	GCTGGTAGAAATGAG[C/T]TGAGTGGTGAGTGAT	54476
rs778797975	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5669844	TAACATCGAGCTGAG[A/G]TCGCACCACTGCACT	54476
rs778818672	snp	G/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676504	ACCTGCATTGAGTAC[G/T]CAGGCCAAGCCAGTG	54476
rs778818921	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5650634	GGCTACCTCAATCCT[G/T]GGCTCATGGCCACCT	54476
rs778852351	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5775467	CTGTAGTGCCCCTGG[A/C]TCTCCAGAATACTTC	54476
rs778856452	in-del	-/TTTTG			upstream-variant-2KB	RNF216	GRCh38.p7	7:5783113	GAGGTGGGAGGATTT[-/TTTTG]TTTTGTTTTGTTTTG	54476
rs778863288	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5701789	ACCCAGTGCTGTGCA[C/G]AGCTGCACATCAATC	54476
rs778866932	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5726961	TGTGAGGTAAGGCCA[C/T]TCCGCCTGCAAGAGA	54476
rs778886549	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5739882	GTGGTATGTGCCTGT[A/G]ATCCCAGCTACTCGG	54476
rs778896399	in-del	-/A			intron-variant	RNF216	GRCh38.p7	7:5776899	AGGGAGACTCTGTCC[-/A]AAAAAAAAAAAAAAA	54476
rs778902197	snp	A/C/T			intron-variant	RNF216	GRCh38.p7	7:5758538	GACAGCAGGACTGCA[A/C/T]GAGACTTTCAGGAGC	54476
rs778920037	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5640518	TCTTTCCGATCCCCA[A/G]ACAGACCCTATGTGT	54476
rs778934385	snp	C/T	3.41799e-05	0.00413385	intron-variant	RNF216	GRCh38.p7	7:5729603	TTTAGGCAACTGAAA[C/T]GAGAGAGAAGCATAA	54476
rs778950222	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5691146	AACCGTGTGTGTAGA[C/T]GGTGAGCCTGGGTGA	54476
rs778968145	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5730135	ATCAAAAGAAAAAAG[A/G]TATTCCACTCTGGGT	54476
rs778968396	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5738617	GGAGGCTGAGGCAGG[A/C]GAATGGCCTGAACCT	54476
rs778993881	snp	A/T	0.000194566	0.0098613	intron-variant, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711735	CATAATTCAATATAC[A/T]TCTAGAAAAAAATGT	54476
rs779002691	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5707978	GTGATCCACTTGCCT[C/T]GGCCTCCCACAGTGC	54476
rs779003851	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675494	TAAATTTAAAAAAAT[C/T]AGCTGAGTGTAGTGG	54476
rs779016938	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5661869	AATTAATTTGGTCGA[A/G]GTCACAGAGCTTTAG	54476
rs779062827	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5725224	ACTGGCCTGTCCAGA[G/T]GCTCAGCAGACACCT	54476
rs779066109	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5720276	CACACCCCTCCTCCT[C/G]AGCCTACTCAACGTG	54476
rs779080822	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5749439	TACAGGCGTGAGCCA[C/G]CACGTCGGGCCTATA	54476
rs779083822	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5773709	GAGTAGCTGGGACGA[C/T]ACATGCGTGCCACCA	54476
rs779087267	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5657427	ACAAAATTAGCTGGG[C/T]GTGGTGGCGCATGCC	54476
rs779100566	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5647187	TGCTCTGGTGGGAGA[C/T]AGGAGTTTTTGGAAT	54476
rs779106045	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5686789	GACTATTTTTCCACG[G/T]ACAGGGCGTGGAGAG	54476
rs779155102	in-del	-/A	1.64779e-05	0.00287031	intron-variant	RNF216	GRCh38.p7	7:5760992	GGATGAAGTGAGAAC[-/A]AACAACTTACCTTGT	54476
rs779161524	snp	A/C	1.81896e-05	0.0030157	intron-variant	RNF216	GRCh38.p7	7:5741843	GAAATTTTAATAATT[A/C]AATTTCTTTCCTATG	54476
rs779168249	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5709436	ATGGTCCTTCCGTTG[C/T]TGTTGAACTGTTCTC	54476
rs779183486	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5640460	CTGGGCCAATCGCTG[A/T]CACCTCCCTGTGGCT	54476
rs779194444	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5625059	ATTGAAAAAACCCGC[C/G]AAGTGGGTGCCCATC	54476
rs779218485	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5695235	CATCTACAACTGCAA[A/G]TCAAGAGTACCAAAT	54476
rs779231594	snp	A/C			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5670906	GGGAAGGCAGGACTC[A/C]AGGTCTTCCCAAGAC	54476
rs779243852	snp	A/G	1.64838e-05	0.00287083	missense	RNF216	GRCh38.p7	7:5716753	ATCTGTAGGGCAAGC[A/G]AAAAGTCTTCATGCT	54476
rs779272448	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713736	GACAAACACCAAAGA[A/G]AACAAATGGAAAAAG	54476
rs779301890	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5685849	AAGGCTGGACAAAAG[C/T]AAAACATTTTCAGTA	54476
rs779327216	snp	A/T	2.81488e-05	0.00375148	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5730807	GGTTTTCCAGAAGAA[A/T]ATTACAAAGTCTGCA	54476
rs779329332	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5705015	ATAAATGAAAAAACA[C/T]ACTTTAAACTTAGCA	54476
rs779340301	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5704253	CGTATTAATATAAAC[A/G]CCTCATTTCAGAGCG	54476
rs779377543	in-del	-/GGTG			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754119	GTTTTTCTTTTGTGT[-/GGTG]TGTGTGTGTGTGTGT	54476
rs779380490	snp	A/G	3.29457e-05	0.00405854	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741444	AGTTTCCAAAGGATC[A/G]CTTTCTGTGTAAAGA	54476
rs779384547	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5634929	ATTTGCAGCTTCATT[C/G]ATCCATGGGGAAAGA	54476
rs779401862	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5752408	AATTGCTCTATAAAT[A/G]TAACAGGAAGATTTG	54476
rs779402624	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5660799	GGTCTCAAACTCCTG[A/G]AGTCAAGCAATCCGC	54476
rs779415692	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5694187	AAGGGCATTTTGTAA[A/G]CTTTCCATTTTAGGA	54476
rs779439899	snp	C/G	1.87746e-05	0.00306381	intron-variant	RNF216	GRCh38.p7	7:5624154	AATGAGAAGGATGAA[C/G]CTGTAGCTTCATGCA	54476
rs779467639	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5762775	AGGACAGTGACTATT[G/T]CTGGGTAAGGGAGAA	54476
rs779476296	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5628774	GATGCACCCAACCTT[A/G]GTCTCCCCAAAATGT	54476
rs779504690	snp	C/T	1.64768e-05	0.00287021	missense	RNF216	GRCh38.p7	7:5641292	ACCACAGCGGCAAGA[C/T]ATGCGGTTGCAGCCT	54476
rs779519196	snp	C/G	3.57603e-05	0.00422834	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622856	CAATGGGGATTCGGG[C/G]CCATCAGAAGCGATG	54476
rs779527143	in-del	-/TT			intron-variant	RNF216	GRCh38.p7	7:5709447	GTTGTTGTTGAACTG[-/TT]CTCTCTATGGGAAAA	54476
rs779537129	snp	A/G	3.53326e-05	0.00420298	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739287	TTACACATTCAGATC[A/G]TAATAATTCTTAAAA	54476
rs779546170	snp	C/G	1.9287e-05	0.00310534	intron-variant	RNF216	GRCh38.p7	7:5752795	GAGTGGCTGAAAAAT[C/G]AGATCACCAACTTGC	54476
rs779548636	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5742769	TCCAGCTAATTTTTC[G/T]ATTTTTGTTAGAGAC	54476
rs779554416	in-del	-/AAAT			intron-variant	RNF216	GRCh38.p7	7:5734833	TCTCTCAAAATAAAT[-/AAAT]AAATAAATAAATAAA	54476
rs779557968	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5722894	AATTCCAGCTACTTG[C/T]GAGGCTGAGGCAGGA	54476
rs779566862	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5764307	AAATAAAACCACACA[C/T]AAAAATGTCATAAGG	54476
rs779580893	snp	G/T	1.64776e-05	0.00287028	synonymous-codon	RNF216	GRCh38.p7	7:5761007	AAACAACTTACCTTG[G/T]CCCCGATGGCAGTGA	54476
rs779601924	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5689037	CTTGGTTCTGCTGTG[A/G]CTTCCTCTCTCATAA	54476
rs779614144	snp	A/G	1.73246e-05	0.00294312	intron-variant	RNF216	GRCh38.p7	7:5725273	CTGACTGTGAAGAAG[A/G]AAAGGTACAGTGTTG	54476
rs779619326	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5733327	GACACAAAAAGCACA[C/G]AGGGTCAGCAAGTCC	54476
rs779636733	snp	A/G	3.78508e-05	0.00435017	intron-variant	RNF216	GRCh38.p7	7:5641410	ATTTGGAGCTGGGAG[A/G]GAAGATGAGGAGGAA	54476
rs779640907	snp	C/G			downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619762	GCCTGCAAAAGAAAC[C/G]GACTGCACCTTTCTT	54476
rs779644280	in-del	-/G			intron-variant	RNF216	GRCh38.p7	7:5701997	GAGCACCAGGATGTT[-/G]TCTGGGACAAGGAAG	54476
rs779654414	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5755463	TCACCACCACAAGGT[C/G]AGGAAATATTTCTAG	54476
rs779666149	snp	C/G	2.36253e-05	0.00343687	intron-variant, utr-variant-5-prime	RNF216	GRCh38.p7	7:5739499	TGTCTTCAAATTCAA[C/G]ACTAGTTCCCAGATT	54476
rs779670847	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5638094	CCTCCTAGACCCAGA[C/G]GTCTGGATGCTCCAT	54476
rs779697674	snp	C/G	1.6473e-05	0.00286988	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741599	ATTCAGAGATTCCAG[C/G]AGGCCCAAGATCCAG	54476
rs779699067	snp	C/T	1.64933e-05	0.00287165	synonymous-codon	RNF216	GRCh38.p7	7:5715128	GTGAGCATCTGCGCA[C/T]TGCGTCAGCTCCTCG	54476
rs779731331	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5747415	CCTGAGGATGATATT[C/T]AGGACCTGACAAGTA	54476
rs779733535	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664678	GCTGTGGAAGGCCAG[C/T]TGCCGCCCAAGGGTA	54476
rs779796716	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5698634	CATAACCTCAAGCAA[C/T]CCTCCTGCCTCATTC	54476
rs779797598	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5683913	AGCCTGCACAGAGAA[C/T]AGGGACGGGCATCAC	54476
rs779817111	snp	C/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754218	TGCAGTACAATGGTG[C/T]GATCATAGCTCACTG	54476
rs779817820	in-del	-/AAAG			intron-variant	RNF216	GRCh38.p7	7:5775247	GAAAATATGGGAAAC[-/AAAG]GAAGTCAGGAAGAAA	54476
rs779849959	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5647968	AGGCCATGACATTCA[C/T]TTGCTTAGAAGTATT	54476
rs779857578	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664185	ATGGGCAAAAAAAGC[A/G]TATCTATCTCCTCTC	54476
rs779861149	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5761545	ACAATCCCAGCACTT[G/T]GGGAGGCCGAGGCGG	54476
rs779865333	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5637606	GGCAGAAGTGTAGTG[A/G]CGCAGTCAGGGCTCA	54476
rs779892183	in-del	-/AC			intron-variant	RNF216	GRCh38.p7	7:5706251	AAAATTGTGGTGAAA[-/AC]ACACAATACAAAAAC	54476
rs779927911	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5740312	TTAATTTTTTTAGTA[C/G]AGACAGGGTTTCACC	54476
rs779933564	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5740341	CCGTGTTAGCCAGGA[C/T]GGTCTTGATATCCTG	54476
rs779936524	in-del	-/ACCACC			intron-variant	RNF216	GRCh38.p7	7:5739231	TATTACATATATTTT[-/ACCACC]ACCACCACCACCACA	54476
rs779945060	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5653813	AACGATGAATAGGGC[A/G]GCGAAAACAGATCAA	54476
rs779958992	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5641585	ACTCACCTGCCTGGA[G/T]ACTCAGTTTCCTCAT	54476
rs779962596	in-del	-/G			intron-variant	RNF216	GRCh38.p7	7:5645027	TCATCATATTGGCCA[-/G]GGTCATCTCGAACTC	54476
rs779974880	in-del	-/TGTTT			intron-variant	RNF216	GRCh38.p7	7:5695423	ATCGCCTTCCTCTCC[-/TGTTT]TTTCTTATGGCTGCT	54476
rs779980675	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5702410	TTTTATTCATATTGG[C/T]GTTTTGTTATAATGC	54476
rs779985350	snp	A/G	1.6483e-05	0.00287076	intron-variant	RNF216	GRCh38.p7	7:5652520	GGTTTCCTGGGGATA[A/G]AGGACAGACACAAAG	54476
rs780001979	snp	A/C			upstream-variant-2KB	RNF216	GRCh38.p7	7:5781957	ATATCTACTGATTTG[A/C]CCTAATTCGTTTGGC	54476
rs780033673	snp	A/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754665	CCCTGCACCCGCAGG[A/G]AATTGTAGATTCCTC	54476
rs780040270	snp	C/T	1.64833e-05	0.00287078	synonymous-codon	RNF216	GRCh38.p7	7:5716743	TTCTTCATTCATCTG[C/T]AGGGCAAGCAAAAAG	54476
rs780040792	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5750588	CCTGAAGCCCTATAA[C/G]CTGAAGCTGGACAAA	54476
rs780046771	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5632754	TGCATTCCAGCCTGG[A/G]CGACAAGAGCAAAAC	54476
rs780059376	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5773728	TGCGTGCCACCATGC[A/T]GGTTAATTTTTGTAT	54476
rs780065096	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5657375	GAGTTCGAGACCAGC[C/G]TGACCAACAGGGAGA	54476
rs780086901	snp	C/T	1.64732e-05	0.0028699	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741204	CCTTGGAAAAGCGGG[C/T]CCTGGGAATTCATGC	54476
rs780088912	snp	C/G	1.6476e-05	0.00287014	missense	RNF216	GRCh38.p7	7:5729446	CCTTTCGGGTGATTG[C/G]ATAGTGTCCTTTGAG	54476
rs780100174	snp	A/G	1.65165e-05	0.00287367	missense	RNF216	GRCh38.p7	7:5623059	GGTGGGTGCGCGAAG[A/G]CATAGGGTGGCATCT	54476
rs780101975	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5701909	TCTTCATGTGAATGG[A/G]ACAGGAGGTTCGTGA	54476
rs780111278	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5642561	TTCCTGGGTTCAAAC[A/G]GTTCACATGTCTCAG	54476
rs780140034	snp	A/G			utr-variant-3-prime	RNF216	GRCh38.p7	7:5622281	TGCTGCCTCATCTGA[A/G]TAGGTGTAAGAGGGG	54476
rs780148312	snp	A/G	1.64732e-05	0.0028699	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741158	GCTGAGGAGAAGAGG[A/G]GCCTGAAATCCCACC	54476
rs780194898	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5717259	TTGGGAGGCTGAAGC[A/C]GGAAGATTACTTGAA	54476
rs780195749	snp	C/G/T	3.31945e-05	0.00407383	intron-variant	RNF216	GRCh38.p7	7:5721199	ACGACAATGCAAAAG[C/G/T]ATGCAGACAACTATG	54476
rs780202325	snp	C/T	1.64727e-05	0.00286986	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741269	GCCGTTCCTGAGGAA[C/T]GACCTGGTTTGTTAT	54476
rs780206929	snp	C/G			upstream-variant-2KB	RNF216	GRCh38.p7	7:5783371	CTGACCTCAGGTAAT[C/G]TACCCACCTCGGCCT	54476
rs780260724	snp	A/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667540	CATCCTGCAGGAGCA[A/G]GGCCATGCATAGGAA	54476
rs780263734	in-del	-/C			intron-variant	RNF216	GRCh38.p7	7:5630925	CTGTTAACCACATAA[-/C]CCCCTCAGGTTTCTG	54476
rs780264175	snp	A/G	5.25841e-05	0.00512731	intron-variant	RNF216	GRCh38.p7	7:5729623	GAGAAGCATAAAATC[A/G]GAGGCCAGGCAGTAC	54476
rs780266582	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5651790	AGTAGCTGGGATTAC[A/C]GGCAAGCGCCACCAT	54476
rs780268037	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5686854	GCAACTCAGATCCCT[C/T]GCATGAGCAGTTCAC	54476
rs780280087	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5710463	ACTTTCACTGGCAGA[C/T]CTTCTTTGAAACCTT	54476
rs780300302	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5718376	ACAAAGCGAGACTCC[A/G]TCTCAAAAAACAAAC	54476
rs780346814	snp	C/T	1.65405e-05	0.00287576	missense, intron-variant	RNF216	GRCh38.p7	7:5741758	CCAACCTTTTCAGAT[C/T]TTGCCACTGGGCAGC	54476
rs780363518	snp	A/G			intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681649	TCAAGGACGAGTCCC[A/G]TTCCTCAACTGGGGA	54476
rs780365536	snp	G/T	1.65974e-05	0.0028807	missense	RNF216	GRCh38.p7	7:5725327	AGTTTGCATTACCTT[G/T]TTCAAACTTGAAATC	54476
rs780392220	snp	A/G	0.000209139	0.0102238	intron-variant	RNF216	GRCh38.p7	7:5760455	CAGGAGGCGGAGCTC[A/G]TGGTGAGTCGAGATT	54476
rs780415286	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5770612	TTTATCAGGTTTTAA[G/T]AATAGATATATACTA	54476
rs780417500	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5695682	TGGTTTTGGCAGCCA[C/G]AGAATAGTGTTCTCC	54476
rs780418157	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5711160	CTAAGTGGCTTCTAA[A/G]TAGCTGAAAGATTTT	54476
rs780458295	snp	A/G	1.64732e-05	0.0028699	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741300	TTCACGGGGCTGTTG[A/G]TTCAGAGACTGGAAG	54476
rs780463477	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5695394	CCAGTCTGAGGGCCC[A/G]GCAGAAGCGCCACAT	54476
rs780464199	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5779544	CTCCCTTCTCAGCGC[G/T]TAAAGAATGTTCTGG	54476
rs780464431	snp	C/G			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5662763	ATGGTGAGTACCTCA[C/G]AGGAAACTAAAGCCA	54476
rs780467152	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5775635	AAAACTTTGAGAGGC[C/T]GAGGTGAGTGGATTA	54476
rs780476440	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5720397	GTTTTCTCTAGCTTA[A/C]CTTATTCTAAGAATA	54476
rs780482730	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5722384	TTTTTTTTTTTGTTT[-/T]GTTTGTTTGTTTTGT	54476
rs780523336	snp	C/T	1.64776e-05	0.00287028	missense	RNF216	GRCh38.p7	7:5761003	GAACAAACAACTTAC[C/T]TTGTCCCCGATGGCA	54476
rs780523924	snp	A/C			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676559	GTCCGTCCTGTCTGC[A/C]TGGCTGTGTGACCAA	54476
rs780534871	snp	C/G	4.04727e-05	0.0044983	intron-variant	RNF216	GRCh38.p7	7:5624017	GCCTGCATGGCCTGG[C/G]TGCTGCTCTGTCCTG	54476
rs780575152	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5706077	TGCAAAAAATTAGCC[A/G]GGCATGGTGGCATGT	54476
rs780600619	snp	C/T			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5753791	CATGAGGTCAGGAGT[C/T]TGAGACCAGCCAGAC	54476
rs780620626	in-del	-/TT			intron-variant	RNF216	GRCh38.p7	7:5659953	AATTACATTCATTAA[-/TT]TTTTTTTTTTTTTTT	54476
rs780621336	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5766563	GAGAAGGCAGTTGTC[C/T]GAGATCCAGGAAGAG	54476
rs780639560	in-del	-/AGC			intron-variant	RNF216	GRCh38.p7	7:5737862	TGAGAGGTGGAGGTG[-/AGC]AGATCATGAGGTCAG	54476
rs780643080	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5727211	GTGATCTCATCTCTC[C/T]TTCAATGCCAGCCCC	54476
rs780644017	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5632611	GCGAAACCCCATCTC[C/T]ACTAAAAATACAAAA	54476
rs780653854	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5778638	TCACTAATTATAGAA[C/G]GATAATTAGTGGCAT	54476
rs780676641	in-del	-/A/AA	0.445367	0.239419	intron-variant	RNF216	GRCh38.p7	7:5760522	CCATCTCAAAAAAAG[-/A/AA]AAAAAAAAAAAACAA	54476
rs780678121	snp	C/G	1.64732e-05	0.0028699	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741492	GATGATGACTTTCTG[C/G]TCTGATCTGGGGTTG	54476
rs780693172	snp	C/G	1.65127e-05	0.00287334	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5752939	TTCCTCATCTGAGGA[C/G]TCAGATATGGTGATG	54476
rs780697986	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5634998	GTTCATGGGGCTCAG[A/G]GACCCTATGGGCACC	54476
rs780703169	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5656197	TTGCTTGAACCCAGG[A/C]GGTGGAGGTTGCATT	54476
rs780710984	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5654585	CCAGCTACTTGGGAG[A/G]CTGAGGCAGGAGAAT	54476
rs780713902	snp	C/G	1.64898e-05	0.00287135	synonymous-codon	RNF216	GRCh38.p7	7:5641169	AGTGGGATCGGTCCA[C/G]AGAGAGCATCTTGAA	54476
rs780729500	snp	C/G	1.64879e-05	0.00287118	utr-variant-5-prime	RNF216	GRCh38.p7	7:5761096	GACATGCATATATGG[C/G]ACTGCTAATATCTAA	54476
rs780756396	in-del	-/GTGT			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5754124	TCTTTTGTGTGGTGT[-/GTGT]GTGTGTGTGTGTGTG	54476
rs780765305	snp	A/C/T	6.86429e-05	0.0058581	intron-variant	RNF216	GRCh38.p7	7:5715014	CTTAGACTCCAGGAA[A/C/T]GTGTCCTATATACAT	54476
rs780806861	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5649967	AATAGGATAACACAC[C/T]GTTCTACTTGAACGA	54476
rs780812571	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5666379	GGGAAGGCCTCTCTG[C/T]GAAGGTGCATGTAAG	54476
rs780820138	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5630232	AAAGCAGTGCTGGCT[C/T]CTTCAAGAGAGGCTG	54476
rs780829729	in-del	-/TAAAA			intron-variant	RNF216	GRCh38.p7	7:5705917	CATCTCAACAAAAAC[-/TAAAA]CAAAACAAAACAAAA	54476
rs780841105	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5691046	TGTCGTCTCTTCCCA[A/G]CTCACACAGCCGTGC	54476
rs780868992	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5738000	GACTGAGCAGGAGAA[C/T]TGCTTGAACCTGGGA	54476
rs780877344	snp	A/C			intron-variant, upstream-variant-2KB	RNF216, MIR6874	GRCh38.p7	7:5713539	CCAGGCAGGAGGCAG[A/C]CTGAATCACCCCAGG	54476
rs780901134	snp	C/T	1.64732e-05	0.0028699	synonymous-codon, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741144	TAGAGGATGGGCAGG[C/T]TGAGGAGAAGAGGGG	54476
rs780901680	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665891	AAGACCAAGGCCGGG[C/T]GCGGTAGCTCACATC	54476
rs780931267	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5699995	ACAAGAAATTCCACC[C/T]AACAGCAGCTTCAGC	54476
rs780958120	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5657128	AGTACAAACTGCTCC[C/T]TTACTTTTAAATGGT	54476
rs780972229	snp	A/C			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668146	TTATATAGCAGGCAT[A/C]GAAAAGCGGCTGCCC	54476
rs780982998	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5706551	TATCTGTGTTGTTAG[C/T]ATGTGCCAGGAGTTC	54476
rs781014559	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5628993	CTTGAGGCCAGGAGT[C/T]AAGAGACCAGTGTGG	54476
rs781019137	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5690050	GGTTTTATGGCCAGG[A/C]GCGGTGGGTGGCTCA	54476
rs781037100	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5684227	CCCACCTCAGCCTCC[A/G]GAGTAGTTAGGACTA	54476
rs781040171	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5719157	CGGCTGAGTTGGGAG[A/G]ACGGCTTGAGGCCAG	54476
rs781047303	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5774332	TCCCAGCTTTACTGT[G/T]GTTGCTGAAGCAAGA	54476
rs781048909	snp	A/C			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673342	GAACAGGCTCGACAG[A/C]ATGGAGTGGGCTGGA	54476
rs781059493	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5773631	GGAGTGCAGTGGCAC[A/G]ATCTCAGCTCACTGC	54476
rs781068791	snp	G/T			intron-variant	RNF216	GRCh38.p7	7:5633628	AAGCGGATTGCATTT[G/T]AACAGGGAGGGAGAT	54476
rs781071313	snp	A/G	1.64868e-05	0.00287109	synonymous-codon	RNF216	GRCh38.p7	7:5622995	TGGGATAGGCCCCAT[A/G]TTGAGTGGGAAGTTG	54476
rs781089807	snp	C/T	1.67323e-05	0.00289239	intron-variant	RNF216	GRCh38.p7	7:5725464	AGAAAAGGAAAGGTT[C/T]CTTCTGTAAATAGAA	54476
rs781115519	snp	A/C			intron-variant	RNF216	GRCh38.p7	7:5693115	ACGCTATGGTATATG[A/C]TACGGGTTGGCAAAC	54476
rs781118218	snp	A/G	2.93733e-05	0.00383221	intron-variant, downstream-variant-500B	RNF216, MIR6874	GRCh38.p7	7:5711721	GCAGCCCATAATACC[A/G]TAATTCAATATACAT	54476
rs781126752	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5685032	AGAGAGTGCCCAGGA[C/T]TCTTGCTGATGGTGA	54476
rs781127013	snp	C/T			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674394	AAACTCCTGACCTCA[C/T]GATCCGCCTGCCTCA	54476
rs781130024	snp	C/T	3.34342e-05	0.00408852	intron-variant	RNF216	GRCh38.p7	7:5715222	AACACACATGAAATG[C/T]CCTGCACTTAAGGAG	54476
rs781239242	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5708621	AAGATTTTGCTAAAT[C/T]GTAGGCTAATATAAG	54476
rs781256557	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5772085	CTAAAAATACAAAAT[C/T]AGCTGGGCATGGTGG	54476
rs781264493	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5728839	AGGTCTCTGCTGGTG[C/T]GTGCGCTCCTGTTCT	54476
rs781277080	snp	C/G			intron-variant	RNF216	GRCh38.p7	7:5771052	ACCTTGTGATTCGCC[C/G]ACCTTGGCCTCCCAA	54476
rs781279616	snp	A/T			intron-variant	RNF216	GRCh38.p7	7:5762343	GCCTGGCCAACATGG[A/T]GAAACCCCATCTCTA	54476
rs781290798	snp	A/C/T	3.50154e-05	0.0041841	intron-variant	RNF216	GRCh38.p7	7:5741827	TTGTCTAAGAAAAAA[A/C/T]GAAATTTTAATAATT	54476
rs781302423	in-del	-/CACAG			intron-variant	RNF216	GRCh38.p7	7:5684995	TTTGAGCAGTCTTTA[-/CACAG]CATAGGTGGAGGGGT	54476
rs781306757	snp	C/T			intron-variant	RNF216	GRCh38.p7	7:5702690	AAACCTTCCCAGGAT[C/T]AAGAAGTCTGTGATG	54476
rs781312375	in-del	-/A			intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663897	GAGGGAGTCCGTCTC[-/A]AAAAAAACAAAACAA	54476
rs781341328	in-del	-/A/AA	0.00840454	0.0643284	intron-variant	RNF216	GRCh38.p7	7:5760514	GTAAAATTCCATCTC[-/A/AA]AAAAAAAGAAAAAAA	54476
rs781373409	snp	C/G			intron-variant, upstream-variant-2KB	RNF216	GRCh38.p7	7:5767032	CATAACACAGCTAAT[C/G]CTAACAAGAACCCTA	54476
rs781378141	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5750065	TGCAAACTATTCATG[A/G]GTATTCTTATTTTTA	54476
rs781379803	in-del	-/T			intron-variant	RNF216	GRCh38.p7	7:5659954	ATTACATTCATTAAT[-/T]TTTTTTTTTTTTTTT	54476
rs781396306	snp	A/C/G	9.88344e-05	0.00702912	missense, utr-variant-5-prime	RNF216	GRCh38.p7	7:5741233	GCTGAAACAACAAGC[A/C/G]GCCCAGTTCTGCTTC	54476
rs781406365	snp	C/G	0.000241167	0.0109784	intron-variant	RNF216	GRCh38.p7	7:5760439	GAGAATCATTTGAAC[C/G]CAGGAGGCGGAGCTC	54476
rs781416037	snp	C/T	3.51803e-05	0.00419391	missense	RNF216	GRCh38.p7	7:5623147	TCTCCACAGGCTTCT[C/T]CAGCGGGGGTCCAAT	54476
rs781424199	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5701966	TAACCCAGGAAGGCA[A/G]CTCAGGACCAGAAGG	54476

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