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

RNF217

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs471429	snp	C/G	0.345704	0.230956	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087885	AAAAGAAATCTCCCT[C/G]ACTAAAAATATGATC	154214
rs472505	snp	G/T	0.0584853	0.160693	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088070	ATGTTGCCCAGGCTG[G/T]TCTCAAACTCTTGGG	154214
rs473130	snp	A/G	0.0667028	0.170006	intron-variant	RNF217	GRCh38.p7	6:125055265	GGGGCAGTCTCTCAA[A/G]TGAATACAAATAAGT	154214
rs473306	snp	C/G	0.223522	0.248594	intron-variant	RNF217	GRCh38.p7	6:125031244	gatgctaggagctgc[C/G]atgaaggcctctgac	154214
rs474025	snp	A/G	0.498206	0.0298983	intron-variant	RNF217	GRCh38.p7	6:125051280	AGACCCAATGACAAT[A/G]GGATAAAGGGAAAAC	154214
rs475076	snp	A/G	0.0150982	0.0855637	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125057966	CCTACCTGCCAATTC[A/G]TCTGGTGTTTTAAGT	154214
rs475133	snp	C/T	0.107694	0.205546	intron-variant	RNF217	GRCh38.p7	6:125031412	TTTTCCAAACATTTA[C/T]GCTGTTTCCCTTTTA	154214
rs476080	snp	C/T	0.101301	0.200969	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081863	ATCAAGGAAAAGAAG[C/T]TCTGCACCTTATGTG	154214
rs478591	snp	C/T	0.0535932	0.154675	intron-variant	RNF217	GRCh38.p7	6:125051756	CCTCTTGCTACTTTA[C/T]GTGGGTACCTCTTGT	154214
rs478948	snp	C/T	0.489201	0.0726845	intron-variant	RNF217	GRCh38.p7	6:125031885	tccattttcacactt[C/T]tgacaaagacataca	154214
rs479063	snp	C/T	0.0670745	0.170406	intron-variant	RNF217	GRCh38.p7	6:125077228	TCCTCCACTCATTCA[C/T]GGAGGACCTGCAATA	154214
rs482014	snp	C/T	0.49607	0.0441545	intron-variant	RNF217	GRCh38.p7	6:125044149	AGTCTTCATAGCATG[C/T]TTTTCTACTCCAAGT	154214
rs484003	snp	A/G	0.109814	0.206997	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092107	TTCCTGCCAACAGGT[A/G]GGTCCTGCTGGACAG	154214
rs484433	snp	C/T	0.101658	0.201233	intron-variant	RNF217	GRCh38.p7	6:125082771	TCTTCTTTGTATGTT[C/T]GTACACTGCAAATAA	154214
rs484636	snp	A/G	0.479258	0.0997024	intron-variant	RNF217	GRCh38.p7	6:125071253	AATTCAAAATTTGAA[A/G]TATGGTTTCTACCAA	154214
rs484822	snp	C/T	0.0505692	0.150756	intron-variant	RNF217	GRCh38.p7	6:125077886	GTGAACCATTTTCCT[C/T]CTTAGAAGCATATGA	154214
rs485640	snp	A/T	0.499987	0.00259581	intron-variant	RNF217	GRCh38.p7	6:125044502	CCTCCCTTCTCTCCT[A/T]ATCTAGCTTCGTAGT	154214
rs487403	snp	A/G	0.0704125	0.17392	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087572	TGGAGACAGTATACA[A/G]AGTTAAAGCAACTGA	154214
rs489245	snp	A/G	0.0667028	0.170006	intron-variant	RNF217	GRCh38.p7	6:125054333	TGAGGTTTAGTCTAA[A/G]GCTCCATGGGGAGCA	154214
rs491270	snp	A/T	0.477768	0.103061	intron-variant	RNF217	GRCh38.p7	6:125070258	tccactcattgattg[A/T]tgggtacttagattg	154214
rs492800	snp	C/T	0.499928	0.00598999	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081565	GCCATAGAGAGAATA[C/T]GAGTGTAAATGTAAT	154214
rs494856	snp	A/G	0.477768	0.103061	intron-variant	RNF217	GRCh38.p7	6:125073609	TTTCTTGCCCAAATC[A/G]TGATTTGTTGGTAAC	154214
rs495548	snp	C/T	0.485118	0.0849685	intron-variant	RNF217	GRCh38.p7	6:125073628	TTTGTTGGTAACTCT[C/T]GACCCTAGGTGCTTA	154214
rs495860	snp	C/G	0.0995161	0.199636	intron-variant	RNF217	GRCh38.p7	6:125075899	CATATATAACATACA[C/G]TGTGGTAGTCACCGC	154214
rs496878	snp	G/T	0.0670745	0.170406	intron-variant	RNF217	GRCh38.p7	6:125075790	GAAAGATATTGTATA[G/T]AAATTAGAGCCATCT	154214
rs497277	snp	G/T	0.447162	0.153712	intron-variant	RNF217	GRCh38.p7	6:125054956	TATCTCACAACCACA[G/T]ACCCACCACATGGAG	154214
rs497574	snp	A/G	0.482534	0.0918038	intron-variant	RNF217	GRCh38.p7	6:125075764	CATCTTTATCTGTGC[A/G]TACTTTGTTGCATGA	154214
rs497969	snp	C/T	0.109461	0.206758	intron-variant	RNF217	GRCh38.p7	6:125038895	aaccaccatggcaca[C/T]gtttacctatgcaac	154214
rs499176	snp	A/C	0.487305	0.0786545	intron-variant	RNF217	GRCh38.p7	6:125058280	AAAATTTTTATAAAC[A/C]ATGTATATTCTTATT	154214
rs500439	snp	C/T	0.0648419	0.167978	intron-variant	RNF217	GRCh38.p7	6:125079329	AAAAATTCTAAGTTT[C/T]AAATCAAGTCGTATA	154214
rs501934	snp	A/G	0.109814	0.206997	intron-variant	RNF217	GRCh38.p7	6:125031997	AAAGGCACTCCTTAC[A/G]TGGCAGCAGCAAGAG	154214
rs502056	snp	C/T	0.482234	0.0925596	intron-variant	RNF217	GRCh38.p7	6:125065166	CGTAGTGGCAGTCGC[C/T]TGTAGTCCCAGCTAC	154214
rs502837	snp	C/T	0.108402	0.206034	intron-variant	RNF217	GRCh38.p7	6:125032094	tagcatgggaaagac[C/T]ggccccccatgattc	154214
rs502889	snp	A/G	0.143284	0.226079	intron-variant	RNF217	GRCh38.p7	6:125027007	aaatgttaaaaaata[A/G]tttaaaaaatttaaa	154214
rs502940	snp	A/T	0.155987	0.23165	intron-variant	RNF217	GRCh38.p7	6:125026995	ATAGTTTAAAAAATT[A/T]AAAAAAGAATGGTAC	154214
rs503812	snp	A/C	0.14665	0.227637	intron-variant	RNF217	GRCh38.p7	6:125042744	GCCTTGGATTGCTCT[A/C]GTCCCTAAACTGCAT	154214
rs503819	snp	C/T	0.452227	0.146984	intron-variant	RNF217	GRCh38.p7	6:125058788	CCAGAAAACTTTGGA[C/T]TTGATGTCTATAGTA	154214
rs504637	snp	A/G	0.067446	0.170804	intron-variant	RNF217	GRCh38.p7	6:125054151	TATGGAACTTCCATT[A/G]GGGATGTAGATGTCT	154214
rs506058	snp	A/C	0.492727	0.0598633	intron-variant	RNF217	GRCh38.p7	6:125044620	CTATATAATGAGAAT[A/C]ATAGGAACAAGTAAG	154214
rs508123	snp	A/G	0.109814	0.206997	intron-variant	RNF217	GRCh38.p7	6:125035247	atgttgaataggagt[A/G]gtgagagagggcatc	154214
rs508732	snp	A/G	0.49533	0.0480965	intron-variant	RNF217	GRCh38.p7	6:125044327	GCTAGAGTATTTTTC[A/G]TAAGTAGTGAACAAT	154214
rs510795	snp	C/T	0.110167	0.207236	intron-variant	RNF217	GRCh38.p7	6:125035520	ggtttgttgtctgca[C/T]gtttctcattgcttt	154214
rs511449	snp	C/T	0.0944967	0.195752	intron-variant	RNF217	GRCh38.p7	6:125078442	GTCATTTATTTGGCT[C/T]ATGGTTCTGGAGGCT	154214
rs512342	snp	C/G	0.47666	0.105476	intron-variant	RNF217	GRCh38.p7	6:125078546	CAAGCCCACGAGACA[C/G]AGAAAATGGGAGCCA	154214
rs518619	snp	C/T	0.0607341	0.163335	intron-variant	RNF217	GRCh38.p7	6:125072654	ATGAGGCAAAACTTA[C/T]TAGAACAAGTTTTTC	154214
rs520292	snp	A/T	0.486133	0.082104	intron-variant	RNF217	GRCh38.p7	6:125074044	ACCTCTCTGTAAGGC[A/T]GAAGCTTACCTGCCA	154214
rs520297	snp	C/G	0.486133	0.082104	intron-variant	RNF217	GRCh38.p7	6:125074048	CTCTGTAAGGCAGAA[C/G]CTTACCTGCCAAGTG	154214
rs521323	snp	A/C	0.222928	0.24853	intron-variant	RNF217	GRCh38.p7	6:125039516	GGAGACTTTAACACC[A/C]CATTTTCAATATTAG	154214
rs522187	snp	C/T	0.109814	0.206997	intron-variant	RNF217	GRCh38.p7	6:125036496	agatccaaaaggaat[C/T]gcaacaaaagccaaa	154214
rs522238	snp	G/T	0.415727	0.187175	intron-variant	RNF217	GRCh38.p7	6:125057362	AAACCCCATCTCTAC[G/T]AAAAATATAAAAATT	154214
rs523217	snp	A/G	0.0696718	0.173152	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086097	GAACATATCCATAAG[A/G]TTGTACATTTGTTTT	154214
rs524695	snp	C/T	0.0700422	0.173537	intron-variant	RNF217	GRCh38.p7	6:125082720	TTAAAGAATGAAATA[C/T]TGAAGAAGTAAATAC	154214
rs524864	snp	C/T	0.100944	0.200705	intron-variant	RNF217	GRCh38.p7	6:125082777	TTGTATGTTCGTACA[C/T]TGCAAATAAATAAAC	154214
rs526790	snp	A/T	0.0700422	0.173537	intron-variant	RNF217	GRCh38.p7	6:125079888	TGTTACTAACCTAGG[A/T]ATAAGAGATAGTATG	154214
rs528201	snp	G/T	0.0611083	0.163768	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092517	TCAAACTATTTTGAT[G/T]GTCATTGTACGAGCT	154214
rs529218	snp	C/T	0.0667028	0.170006	intron-variant	RNF217	GRCh38.p7	6:125059227	GACCTGGCTTTCTAA[C/T]AGAAGTGATGTCTAA	154214
rs529337	snp	A/G	0.0566069	0.158427	intron-variant	RNF217	GRCh38.p7	6:125065831	GCTGTTGGCTCAGTC[A/G]GTAGGCAAATCGTAA	154214
rs530999	snp	C/G	0.0599851	0.162463	intron-variant	RNF217	GRCh38.p7	6:125059402	AATGAGGCCTTCCCC[C/G]CTTTCTCTTGCCTTT	154214
rs537650	snp	C/T	0.478104	0.102316	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090503	AAAGAGAAAAAAATT[C/T]GAGTGTTTATCTGTT	154214
rs539463	snp	A/C	0.489201	0.0726845	intron-variant	RNF217	GRCh38.p7	6:125031884	gtatgtctttgtcaa[A/C]agtgtgaaaatggac	154214
rs539676	snp	G/T	0.478104	0.102316	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090773	AGTTTAAAATGGACC[G/T]GGTTGAAAAGAGATT	154214
rs540840	snp	A/C	0.123452	0.215605	intron-variant	RNF217	GRCh38.p7	6:125071129	ACAACTTGAGGAGGA[A/C]AGGTACTATTTTCTT	154214
rs544426	snp	A/G	0.497933	0.032082	intron-variant	RNF217	GRCh38.p7	6:125071536	TGTGTGTGTGTGTGT[A/G]TATATCTTATTACAG	154214
rs545008	snp	C/T	0.0681886	0.171594	intron-variant	RNF217	GRCh38.p7	6:125050654	TTACACATTCTTATA[C/T]ATGGGAAACAGTTCT	154214
rs545124	snp	A/G	0.0700422	0.173537	intron-variant	RNF217	GRCh38.p7	6:125079792	AAATAGGGAAAAGAA[A/G]CAAAAAATTAAGTAT	154214
rs546893	snp	G/T	0.109814	0.206997	intron-variant	RNF217	GRCh38.p7	6:125036891	ttattatttattata[G/T]ttattatatattatt	154214
rs547130	snp	A/G	0.479095	0.100076	intron-variant	RNF217	GRCh38.p7	6:125071828	ATTTATGAGTGGCCA[A/G]TTTTATCTAATGGAT	154214
rs548862	snp	G/T	0.394354	0.204112	intron-variant	RNF217	GRCh38.p7	6:125050187	CAAGTGCAGACTGAA[G/T]AAATGATCCCCCTTT	154214
rs548865	snp	G/T	0.394171	0.204242	intron-variant	RNF217	GRCh38.p7	6:125050184	TTCCAAGTGCAGACT[G/T]AATAAATGATCCCCC	154214
rs552705	snp	C/T	0.156319	0.231784	intron-variant	RNF217	GRCh38.p7	6:125028989	AACTTCTTGATTTTG[C/T]TATTGGTCAACCAGG	154214
rs554975	snp	A/T	0.109814	0.206997	intron-variant	RNF217	GRCh38.p7	6:125040119	TTTGAAGGTTTTTTC[A/T]TGTCTCTATCTCCTT	154214
rs554999	snp	C/T	0.475437	0.108066	intron-variant	RNF217	GRCh38.p7	6:125066329	AGAGCAAAAGTTAGT[C/T]CTATGATGACCATAG	154214
rs555347	snp	G/T	0.0640965	0.167152	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087292	CAAAAATAAGAAAAT[G/T]TATGCCAAAAAACGT	154214
rs556142	snp	C/T	0.0592355	0.161582	intron-variant	RNF217	GRCh38.p7	6:125050478	TTTCTTTCTTATAAA[C/T]CCTCTGAGTAGAAAT	154214
rs556308	snp	A/G	0.478188	0.10213	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087421	TCTCCCAACTATTGA[A/G]AGTGATCTTTCCCAT	154214
rs556784	snp	C/T	0.110167	0.207236	intron-variant	RNF217	GRCh38.p7	6:125033106	ctatttttCTTTTTT[C/T]TTCTTTTTTCAATAT	154214
rs560739	snp	A/G	0.481473	0.0944461	intron-variant	RNF217	GRCh38.p7	6:125050985	TACCCTTGAAAAAAC[A/G]TATAACACTCAGCTA	154214
rs561365	snp	A/C	0.125634	0.217214	intron-variant	RNF217	GRCh38.p7	6:125067020	TACGAGGGTTCATGG[A/C]GAAAGGACTCAACAC	154214
rs562841	snp	A/T	0.0562307	0.157967	intron-variant	RNF217	GRCh38.p7	6:125070008	ATCCCTTTCCCACTC[A/T]TACCTCCTATTCCTA	154214
rs564516	snp	C/T	0.499942	0.00539106	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081732	ACTGTGATTCATGTA[C/T]CTTATAAAGCATTAT	154214
rs565056	snp	A/G	0.0633504	0.166319	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091204	AAGGAAGAAGTTGGT[A/G]AATAAAAGCCAGGGA	154214
rs565968	snp	C/T	0.470521	0.117772	intron-variant	RNF217	GRCh38.p7	6:125060977	CTAACATTGCAAACA[C/T]TTCTCATATTACTGA	154214
rs567448	snp	C/T	0.498109	0.0306926	intron-variant	RNF217	GRCh38.p7	6:125053320	AGTAGCAGGAACTGC[C/T]TATGTTGATTGTAGG	154214
rs571846	snp	C/T	0.0532157	0.154195	intron-variant	RNF217	GRCh38.p7	6:125080418	TTGACAAACTTCCAA[C/T]AAATGGCTGTATTAG	154214
rs572110	snp	C/T	0.0667028	0.170006	intron-variant	RNF217	GRCh38.p7	6:125053644	GGTTGTTTCCTTACT[C/T]GACTTGATGAATTAT	154214
rs573804	snp	C/T	0.154993	0.231244	intron-variant	RNF217	GRCh38.p7	6:125049765	AACTATATTCTTTTT[C/T]ACTCCCCCATGCCCT	154214
rs575035	snp	A/C	0.124491	0.216211	intron-variant	RNF217	GRCh38.p7	6:125037955	AATTGAGCAATGAGG[A/C]CTGAGATTTGTACTT	154214
rs576419	snp	A/G	0.479583	0.0989539	intron-variant	RNF217	GRCh38.p7	6:125049480	CTTTTCAACCTTGGT[A/G]AATCCAACACCTCAA	154214
rs576558	snp	G/T	0.190583	0.249022	intron-variant	RNF217	GRCh38.p7	6:125047532	ATGTCTATCAATTTG[G/T]TGTAGGTAAGAAGAG	154214
rs577387	snp	A/G	0.124491	0.216211	intron-variant	RNF217	GRCh38.p7	6:125037953	TAAATTGAGCAATGA[A/G]GACTGAGATTTGTAC	154214
rs580862	snp	A/G	0.105569	0.204058	intron-variant	RNF217	GRCh38.p7	6:125041437	GTATTGTCTTTATAT[A/G]ATACAGACTTTTTAC	154214
rs723051	snp	C/T	0.0240643	0.107019	intron-variant	RNF217	GRCh38.p7	6:125079770	GGTTATGTGCAAGTA[C/T]AATTTAAAATAGGGA	154214
rs723052	snp	C/G	0.0240643	0.107019	intron-variant	RNF217	GRCh38.p7	6:125079869	AAATGATGTTTTAGA[C/G]CAATGTTACTAACCT	154214
rs911966	snp	A/C	0.470715	0.117409	intron-variant	RNF217	GRCh38.p7	6:125070947	GTATACATCTGCCCA[A/C]AAGTATTTGTCTCCA	154214
rs973396	snp	A/T	0.155987	0.23165	intron-variant	RNF217	GRCh38.p7	6:125026656	TAACTGTGATTCCCT[A/T]TTTTTTTTCTCAGAG	154214
rs990788	snp	C/T	0.470618	0.117591	intron-variant	RNF217	GRCh38.p7	6:125069547	cccatcaacagtgga[C/T]tggataaagaaaatg	154214
rs992970	snp	C/T	0.497776	0.0332724	intron-variant	RNF217	GRCh38.p7	6:125043859	TGTTAAAAGTATAAA[C/T]TGTTGCATAATTTTA	154214
rs1044723	snp	A/G	0.152001	0.229992	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091073	TCTTACACTTTTTAG[A/G]GCAATCAACTTATTT	154214
rs1044724	snp	A/C	0.152001	0.229992	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091085	TAGAGCAATCAACTT[A/C]TTTCCAAATTATTAT	154214
rs1322632	snp	A/T	0.00636936	0.0560724	intron-variant	RNF217	GRCh38.p7	6:125080124	GAACAGACTGAGCTA[A/T]GTGCATAGGAGAAAA	154214
rs1322633	snp	A/G	0.340559	0.233022	intron-variant	RNF217	GRCh38.p7	6:125082133	AGTTTCTGACTCGGT[A/G]TATGGGAAAAGTCCA	154214
rs1322634	snp	C/T	0.478685	0.10101	intron-variant	RNF217	GRCh38.p7	6:125082248	TTTTAAGCTAAATGC[C/T]ATAGATAAAGGCTGC	154214
rs1334421	snp	A/G	0.243919	0.249926	intron-variant	RNF217	GRCh38.p7	6:124969572	ACAAATAGTAAGAAA[A/G]ACCATTTATTGGACA	154214
rs1334422	snp	A/T			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982623	GTTTTATAGATCATT[A/T]ATTAATAATATATTT	154214
rs1334423	snp	A/G	0	0	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982730	GGCATTTGGTTTCTA[A/G]ATGATATGCAAACAC	154214
rs1334424	snp	A/G	0.3742	0.216966	intron-variant	RNF217	GRCh38.p7	6:124986940	tttcctgtcatcagt[A/G]ttaattgtaaatatt	154214
rs1334425	snp	C/T	0.376592	0.215579	intron-variant	RNF217	GRCh38.p7	6:124991504	ggctttattatcttc[C/T]aataatgatgtgttt	154214
rs1334426	snp	A/G	0.3742	0.216966	intron-variant	RNF217	GRCh38.p7	6:124995947	AAGAATCAAGAAAAG[A/G]AAAACATTTGGAATA	154214
rs1334427	snp	C/G	0.378962	0.21417	intron-variant	RNF217	GRCh38.p7	6:124997557	CACATTGATGAAGGG[C/G]AAGTCAGAGTGGAAA	154214
rs1334428	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125008343	catagttgaccacaa[A/G]taagtgaaatcatgg	154214
rs1334433	snp	C/T	0	0	intron-variant	RNF217	GRCh38.p7	6:124966485	GCAAATGTGTCAAGC[C/T]TAAACTTTCAGGGTT	154214
rs1413594	snp	A/G	0.226188	0.248863	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982337	GGGATTTAATTTTTG[A/G]ATCATGACAGTTTAG	154214
rs1413595	snp	A/G	0.206336	0.246157	intron-variant	RNF217	GRCh38.p7	6:125012527	TGATTATAATTTAAC[A/G]TGAACCTCATTGATA	154214
rs1413596	snp	A/G	0.121369	0.214369	intron-variant	RNF217	GRCh38.p7	6:125013574	AAAAGTAGTCTGAAA[A/G]CTTTGGCTGTTTTCT	154214
rs1413597	snp	C/G	0.155987	0.23165	intron-variant	RNF217	GRCh38.p7	6:125013607	TAGTAAAGACTTATA[C/G]AGTTCGTATTCAGCT	154214
rs1413598	snp	C/T	0.451856	0.147493	intron-variant	RNF217	GRCh38.p7	6:125015653	TATATATATTGGTAT[C/T]GCTACATCCAGTATA	154214
rs1812965	snp	A/G	0.480618	0.0965156	intron-variant	RNF217	GRCh38.p7	6:125075070	TTGTCCAACCTGTGG[A/G]CCACTTGCTGCCCAG	154214
rs1830651	snp	A/G	0.399611	0.200291	intron-variant	RNF217	GRCh38.p7	6:125047563	AAGCAGGGGCAAATG[A/G]ACCAACATCTTAAAT	154214
rs1931657	snp	A/G	0.139225	0.224118	intron-variant	RNF217	GRCh38.p7	6:125008467	CAGGGTCCATGAATC[A/G]CATGCATACTGCGAG	154214
rs1931658	snp	C/G	0.118235	0.212457	intron-variant	RNF217	GRCh38.p7	6:125015277	AATATATCTTCATTA[C/G]ATGTATTGATTTTAA	154214
rs2039493	snp	G/T	0.492871	0.0592773	intron-variant	RNF217	GRCh38.p7	6:125022451	TGGACTAGGAAGGAT[G/T]AGCAGGCTGACAGGG	154214
rs2093522	snp	A/G	0.123798	0.215808	intron-variant	RNF217	GRCh38.p7	6:125070549	cattcttgtaggagt[A/G]aggtggtatctcatt	154214
rs2151882	snp	A/G	0	0	intron-variant	RNF217	GRCh38.p7	6:124994399	attcttttgaacgga[A/G]acataattacaccta	154214
rs2181281	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125062749	gcccggctaattttt[C/G]tatttttagtagaga	154214
rs2184351	snp	A/G	0	0	intron-variant	RNF217	GRCh38.p7	6:124993898	CAGGAGATCCTCTGG[A/G]GAGGTGAGTGGGAAT	154214
rs2224643	snp	C/T	0.460477	0.134905	intron-variant	RNF217	GRCh38.p7	6:125039861	ctcctgggtaaataa[C/T]gaaattaaggcagaa	154214
rs2246855	snp	C/T	0.155656	0.231515	intron-variant	RNF217	GRCh38.p7	6:125028034	aaactactcctctga[C/T]aagaaattaatcacc	154214
rs2325762	snp	G/T	0.375	0.216506	intron-variant	RNF217	GRCh38.p7	6:124990633	CAATTCTGGTTATAT[G/T]TTAAAGGTAGATCTA	154214
rs2325763	snp	A/G	0.405429	0.195811	intron-variant	RNF217	GRCh38.p7	6:124990326	gaaagccagtggcag[A/G]tacagaatacttacc	154214
rs2325764	snp	A/G	0.3748	0.216622	intron-variant	RNF217	GRCh38.p7	6:124989214	ATTACTAGCATAAGC[A/G]CTCATCAAAATATTG	154214
rs2325765	snp	A/G	0.356169	0.226336	intron-variant	RNF217	GRCh38.p7	6:124988871	TCAACTGACATACAG[A/G]TACGGCTTAACTGTT	154214
rs2325766	snp	C/T			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961696	TAATGCTAAGGATTA[C/T]GAATTCTAAATGCTG	154214
rs2475843	snp	A/G	0.163892	0.234703	intron-variant	RNF217	GRCh38.p7	6:125036773	aaaatgctcatcatc[A/G]ctggtcattagagaa	154214
rs2759261	snp	C/T	0.15665	0.231917	intron-variant	RNF217	GRCh38.p7	6:125027862	ttaactggggtgaga[C/T]ggtatctcttgtagt	154214
rs2759262	snp	C/T	0.156319	0.231784	intron-variant	RNF217	GRCh38.p7	6:125028414	ccattttttattagg[C/T]tattatatatttctt	154214
rs2759263	snp	G/T	0.423413	0.180077	intron-variant	RNF217	GRCh38.p7	6:125029286	AACATCAAAAGCAAA[G/T]ACAGCTTTTTAAAAA	154214
rs2759264	snp	C/T	0.429987	0.173507	intron-variant	RNF217	GRCh38.p7	6:125027294	ccatccctacctccc[C/T]gccaatgcccaacta	154214
rs2759265	snp	C/T	0.156319	0.231784	intron-variant	RNF217	GRCh38.p7	6:125027300	ctacctccccgccaa[C/T]gcccaactacccttc	154214
rs2875692	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124993803	TGACACACTCTTTAC[C/G]CAGCCCCTTCTTTAT	154214
rs3048572	in-del	-/CT	0.348134	0.229934	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961543	ATTTAAAATTTCTCT[-/CT]TTTTCTTCGCCTACA	154214
rs3048573	in-del	-/TTTTGTTTT			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961223	GGAAGCCAGCCCTTG[-/TTTTGTTTT]TTTTCTCCTGAGAGG	154214
rs3080911	in-del	-/A	0	0	intron-variant	RNF217	GRCh38.p7	6:125021269	CAAGACTCCGTCTCA[-/A]AAAAAAAAAAAAAAG	154214
rs3173134	snp	C/T	0	0	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091756	CCTTACAACTTATTC[C/T]TGGCAATATTTTGTC	154214
rs3221828	microsatellite	(CA)17/18/19/20/21/22/23/24	0.763848	0.130604	intron-variant	RNF217	GRCh38.p7	6:125071487	AGATATATATATATA[(CA)17/18/19/20/21/22/23/24]ATATGTAGGCAGATG	154214
rs3927600	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124985183	ATTATATTCTTT[A/G]	154214
rs4464821	snp	A/G	0.288646	0.246995	intron-variant	RNF217	GRCh38.p7	6:125068065	TCATGGATAATATTC[A/G]TGTGTTTTTTTAAAA	154214
rs4555935	snp	C/T	0.491473	0.0647364	intron-variant	RNF217	GRCh38.p7	6:125031031	ttctttgcacatgca[C/T]gcggaacaccacatg	154214
rs4587189	snp	A/C	0.356383	0.226236	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084060	TAGGTCAAGGTCTTA[A/C]ATCATTTAATATCCT	154214
rs4895613	snp	G/T	0.35574	0.226537	intron-variant	RNF217	GRCh38.p7	6:124997547	TGACAGCAGACACAT[G/T]GATGAAGGGCAAGTC	154214
rs4895620	snp	A/G/T	0.566319	0.184215	intron-variant	RNF217	GRCh38.p7	6:125021512	CCTCGTGATCTACCC[A/G/T]CCTCGGCCTCCCAAA	154214
rs4895621	snp	A/C	0.274929	0.248754	intron-variant	RNF217	GRCh38.p7	6:125022992	AGGTATTAGAGATGC[A/C]AGAATAAACAAGGCA	154214
rs4896638	snp	C/T	0.37778	0.214877	intron-variant	RNF217	GRCh38.p7	6:124983785	GGAAAAGATACTTAA[C/T]GGGTTAGTGTCTTAG	154214
rs4896641	snp	A/G	0.3744	0.216852	intron-variant	RNF217	GRCh38.p7	6:124985738	AAATCAGATTTATGA[A/G]TGTCTAGCTCTGGGA	154214
rs4896649	snp	G/T	0.357664	0.225629	intron-variant	RNF217	GRCh38.p7	6:124989389	cttcttttgacgtat[G/T]caatagtaatgagaa	154214
rs5012579	snp	A/G	0.356169	0.226336	intron-variant	RNF217	GRCh38.p7	6:124988868	AATAACAGTTAAGCC[A/G]TATCTGTATGTCAGT	154214
rs5879766	in-del	-/ATAAC	0.45946	0.136478	intron-variant	RNF217	GRCh38.p7	6:125063678	TTTTGCACAATAATT[-/ATAAC]ATAACAGGATTGGTA	154214
rs6149796	in-del	-/ACCTTACCATTGGTAAGTAGCTTTATT/ACCTTACCATTGGTAAGTAGCTTTCTT	0.5	0	intron-variant	RNF217	GRCh38.p7	6:124989059	CAATATAATTTAATT[lengthTooLong]TGCTTGTCTAACAAA	154214
rs6569406	snp	C/T	0.231482	0.249313	intron-variant, upstream-variant-2KB, missense	RNF217, RNF217-AS1	GRCh38.p7	6:124963977	AGTTGAAGTACTTTT[C/T]TTTCACTGAGGTTTT	154214
rs6569408	snp	G/T	0.19459	0.243782	intron-variant	RNF217	GRCh38.p7	6:125023150	GATACAGTTTTGAGG[G/T]ATTACAAAAGGCTTC	154214
rs6569409	snp	G/T	0.340559	0.233022	intron-variant	RNF217	GRCh38.p7	6:125028741	TCACTTAAAAGAGAA[G/T]GGTGTAAGAGCTTTT	154214
rs6569411	snp	A/T	0.0322114	0.122752	intron-variant	RNF217	GRCh38.p7	6:125063080	GTTCGTAATAGTTTT[A/T]ATATTAAATTTAAAG	154214
rs6569412	snp	A/T	0.164873	0.23506	intron-variant	RNF217	GRCh38.p7	6:125072278	ATATTCATAATAATA[A/T]TAAAGGCAGCACTGT	154214
rs6569413	snp	C/T	0.214239	0.247429	intron-variant	RNF217	GRCh38.p7	6:125076066	CAATAGAGGAAGGTG[C/T]TTAGTTGCACAGATG	154214
rs6899594	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124979507	aagataccagcgtgg[C/T]gcagagcaccaaagg	154214
rs6905212	snp	A/G	0.205417	0.245993	intron-variant	RNF217	GRCh38.p7	6:125023409	TTAATTAGTGGAGTT[A/G]TATGATCAGACTTGT	154214
rs6906570	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125071079	CAGTTCTTTTTTTTA[A/G]ATACTTTGTGGGCAT	154214
rs6909569	snp	G/T	0.205417	0.245993	intron-variant	RNF217	GRCh38.p7	6:125023428	GATCAGACTTGTGTT[G/T]TAAAAAGAGTGCTCC	154214
rs6910983	snp	A/G	0.00953873	0.0683987	intron-variant	RNF217	GRCh38.p7	6:125071456	TTTTCAACCTATGAT[A/G]TTTTCAACTTGGAGC	154214
rs6911261	snp	G/T	0.104149	0.203046	intron-variant	RNF217	GRCh38.p7	6:125038242	AGTTGTATTAGCATT[G/T]TACACACGGAGCAGC	154214
rs6911262	snp	A/T	0.108402	0.206034	intron-variant	RNF217	GRCh38.p7	6:125038243	GTTGTATTAGCATTT[A/T]ACACACGGAGCAGCA	154214
rs6911561	snp	A/G	0.471483	0.115954	intron-variant	RNF217	GRCh38.p7	6:125071810	ATTCAAATGTCATTC[A/G]TGATTTATGAGTGGC	154214
rs6912067	snp	A/G	0.471483	0.115954	intron-variant	RNF217	GRCh38.p7	6:125072060	TGTGTTTTAAAAACA[A/G]AGATGACACTGTTAA	154214
rs6912698	snp	A/G	0.373799	0.217195	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981889	aaaatttggccgggc[A/G]tggttatgggcacct	154214
rs6918189	snp	A/T	0.0930568	0.194599	intron-variant	RNF217	GRCh38.p7	6:125026547	TTGAGAGCGTAAACG[A/T]GTCATCAGTACTCCA	154214
rs6920132	snp	A/G	0.0667028	0.170006	intron-variant	RNF217	GRCh38.p7	6:125030848	ctagacggtgcccca[A/G]tagggacactgtgta	154214
rs6921147	snp	A/G	0.472989	0.113031	intron-variant	RNF217	GRCh38.p7	6:125031215	actttttcctccagc[A/G]cctccaggcctgtga	154214
rs6926080	snp	C/T	0.48955	0.071525	intron-variant	RNF217	GRCh38.p7	6:125024492	ggaggctgaggcagg[C/T]ggatcacctgagctc	154214
rs6926311	snp	A/G	0.48679	0.0801892	intron-variant	RNF217	GRCh38.p7	6:125061804	AAATATGTTGCTTCT[A/G]AGTTTAAAAAGTCAT	154214
rs6928650	snp	A/T	0.0581099	0.160244	intron-variant	RNF217	GRCh38.p7	6:124989883	aaaaaaaaaacacca[A/T]caaaataaagacaac	154214
rs6929098	snp	C/T	0.067446	0.170804	intron-variant	RNF217	GRCh38.p7	6:125041047	acaagacaaggatgc[C/T]ctctctcaccactcc	154214
rs6929881	snp	C/T	0.0352966	0.128072	intron-variant	RNF217	GRCh38.p7	6:125078224	ACTAGGGAATCTAAC[C/T]TTAACCTCTAATACC	154214
rs6932035	snp	A/G	0.031825	0.122064	intron-variant	RNF217	GRCh38.p7	6:125062757	aatttttgtattttt[A/G]gtagagacgaggttt	154214
rs6932834	snp	A/T	0.356169	0.226336	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090873	ATTAGTTATACTATT[A/T]ACTTTGATAATCACA	154214
rs6933898	snp	A/C	0.0107246	0.0724382	missense, intron-variant, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962663	GGGACAgcgcccggg[A/C]gcccccgctgcgcgc	154214
rs6941072	snp	A/C	0.442385	0.15965	intron-variant	RNF217	GRCh38.p7	6:124984705	aagacctagatgtgt[A/C]atcaaattttaagtg	154214
rs7454748	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125021498	tcttgaactcctgac[C/T]tcgtgatctacccac	154214
rs7743211	snp	C/T	0.0178098	0.0926698	intron-variant	RNF217	GRCh38.p7	6:125044402	GTTGTGTCCACACTT[C/T]GTGCTTTAATCTTTT	154214
rs7744271	snp	C/T	0.206336	0.246157	intron-variant	RNF217	GRCh38.p7	6:125010882	CTCCCAGGTCTACCA[C/T]GGTACCTAAAATTCT	154214
rs7746049	snp	A/G	0.247053	0.249983	intron-variant	RNF217	GRCh38.p7	6:124998545	TGGCTCAAACCTGTA[A/G]TCGCAACACTTTGGG	154214
rs7746376	snp	A/C	0.0349115	0.127424	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086779	ACACAAGTCAGGTTA[A/C]AACATGATATCTTTA	154214
rs7746860	snp	C/G	0.151001	0.229563	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087075	AGAGACAGGAGGGGC[C/G]TAAAAACTCACTCTG	154214
rs7746892	snp	C/G	0.151001	0.229563	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087117	ACATTAGAATTCCTT[C/G]CTGACCTTTGTCAAA	154214
rs7747579	snp	C/T	0.093417	0.194889	intron-variant	RNF217	GRCh38.p7	6:125053883	TTAGAAGAGTTTGTG[C/T]GTTGATCATAGTGCT	154214
rs7750072	snp	C/T	0.481319	0.0948228	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124968073	AGGCATGAGCCACCG[C/T]GCCTGGCCCCATAAA	154214
rs7751033	snp	A/G	0.157642	0.232314	intron-variant	RNF217	GRCh38.p7	6:125005270	AGCCTCAAACTTGGC[A/G]TCTCAGGTCAGTCAG	154214
rs7753550	snp	A/G	0.3746	0.216737	intron-variant	RNF217	GRCh38.p7	6:124987915	attggattaattaac[A/G]tacattagaaagtct	154214
rs7754082	snp	A/G	0.305436	0.243776	intron-variant	RNF217	GRCh38.p7	6:125018028	AAAGTTTTTATAAGT[A/G]TAACAACTATCCATT	154214
rs7754642	snp	A/G	0.487305	0.0786545	intron-variant	RNF217	GRCh38.p7	6:125076414	TGTGTTTGCTTTTAT[A/G]TTGGTCAAGATAAGC	154214
rs7756487	snp	C/T	0.103794	0.20279	intron-variant	RNF217	GRCh38.p7	6:125000437	GTAAATGTAAGGGGG[C/T]ATTATAGATATCAGA	154214
rs7756705	snp	A/G	0.0134861	0.0810011	intron-variant	RNF217	GRCh38.p7	6:125000717	AGTATCTACATGCCT[A/G]CATTTTAAGGAAGTT	154214
rs7757147	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125000968	GAGAAATGTCTTTCA[A/C]TTACATATAGTGAAA	154214
rs7760717	snp	A/G	0.440746	0.161604	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125006881	ttgaacccaggaggc[A/G]gaggttgcaatgagc	154214
rs7761012	snp	A/C	0.29175	0.246489	intron-variant	RNF217	GRCh38.p7	6:124976890	TATATCACCTTTTGA[A/C]TCATGGAGGCTTTTC	154214
rs7761123	snp	A/G	0.157311	0.232183	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125006898	aggttgcaatgagcc[A/G]agatcgcgccattgc	154214
rs7761517	snp	A/C	0.297128	0.245518	intron-variant	RNF217	GRCh38.p7	6:124977194	TTTCTGACTAGTTGC[A/C]AGATTAACATCAGGG	154214
rs7762807	snp	C/T	0.493925	0.054776	intron-variant	RNF217	GRCh38.p7	6:125023059	GAAAACAAACAATTT[C/T]GCTAGAATAGGATAA	154214
rs7767078	snp	C/T	0.0901694	0.192235	intron-variant	RNF217	GRCh38.p7	6:124978229	attccttctgtgctg[C/T]ttcaccagtcagaaa	154214
rs7767549	snp	A/G	0.0599851	0.162463	intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967843	gagtgcaatggcttc[A/G]tcttggctcactgca	154214
rs7767722	snp	A/G	0.0256215	0.110247	intron-variant	RNF217	GRCh38.p7	6:125055543	TTATAGAGCGAATCC[A/G]AGTTTCAAAGCATCT	154214
rs7768007	snp	A/G	0.0352966	0.128072	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090900	CACAAAACTATGTGG[A/G]AGAAATCATTCTGAT	154214
rs7768186	snp	A/G/T	0.0244538	0.107838	intron-variant	RNF217	GRCh38.p7	6:125055843	CAATGGCAAATGGAA[A/G/T]TAAACATTTTATATT	154214
rs7768477	snp	A/G	0.155325	0.23138	intron-variant	RNF217	GRCh38.p7	6:125003104	ATTTTAAacacacac[A/G]cacacaaacacacac	154214
rs7768636	snp	A/G	0.0486741	0.148216	intron-variant	RNF217	GRCh38.p7	6:125056339	ctaccttccagcatt[A/G]ttttgaggatgaaaa	154214
rs7768650	snp	A/G	0.152001	0.229992	intron-variant	RNF217	GRCh38.p7	6:125003183	CAGATATATGGGTGA[A/G]TAGAAGAGATTTAAC	154214
rs7768909	snp	C/G	0.239614	0.249784	upstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962484	GCCCCCGCTGCCCGC[C/G]GGCGCCGGGTGGGGG	154214
rs7772639	snp	A/G	0.155656	0.231515	intron-variant	RNF217	GRCh38.p7	6:125003546	gattcactgcacagt[A/G]tggtgactgtagtta	154214
rs7772667	snp	A/G	0.201727	0.245295	intron-variant	RNF217	GRCh38.p7	6:125003615	TATTCATAAACATAT[A/G]AGGTGATGGATTTGT	154214
rs7774635	snp	A/C	0.00398564	0.0444627	intron-variant, upstream-variant-2KB, missense	RNF217, RNF217-AS1	GRCh38.p7	6:124963893	TGTATATTCCAGGAA[A/C]GAGTGAATGTTTAAA	154214
rs8180579	snp	C/T	0.344815	0.231323	intron-variant	RNF217	GRCh38.p7	6:125024416	ggtaaaatcccatct[C/T]cactaaaataccaaa	154214
rs9321013	snp	A/G	0.390464	0.206809	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009775	TCTCCGTGCACATTC[A/G]TTGGGAGAACTTTCA	154214
rs9321014	snp	A/G	0.386694	0.20932	intron-variant	RNF217	GRCh38.p7	6:125036844	ttagaatggcgatta[A/G]aaagccaggaaataa	154214
rs9321015	snp	A/G	0.386504	0.209444	intron-variant	RNF217	GRCh38.p7	6:125036926	atttattataaagca[A/G]gaaataacagatgga	154214
rs9321016	snp	C/T	0.127599	0.217986	intron-variant	RNF217	GRCh38.p7	6:125062252	AAGCATTACTTCTCT[C/T]TTAGTGAGTTTTTAC	154214
rs9321017	snp	C/T	0.127599	0.217986	intron-variant	RNF217	GRCh38.p7	6:125062360	AATTTTTATTTATAA[C/T]TGTATTTTGGCAGGT	154214
rs9321018	snp	A/G	0.0345262	0.126772	intron-variant	RNF217	GRCh38.p7	6:125063688	TAATTATAACATAAC[A/G]GGATTGGTAGTATGT	154214
rs9321019	snp	A/T	0.488363	0.0753851	intron-variant	RNF217	GRCh38.p7	6:125075235	CTTCTTCTAGTGTGG[A/T]CAAAAGATTGGACAC	154214
rs9372802	snp	C/T	0.376592	0.215579	intron-variant	RNF217	GRCh38.p7	6:124992529	GCAAGATACTGGATT[C/T]GGTTAGCTTGTTCTA	154214
rs9372803	snp	G/T	0.376195	0.215812	intron-variant	RNF217	GRCh38.p7	6:124992566	TATATAATAAAAGTT[G/T]AGAATAGTGAGAAGA	154214
rs9372804	snp	A/G	0.376394	0.215696	intron-variant	RNF217	GRCh38.p7	6:124994277	GAACTATTTTGTTGC[A/G]TATCTATTCCCACTC	154214
rs9372806	snp	C/T	0.440333	0.16209	intron-variant	RNF217	GRCh38.p7	6:125046857	TAGTTAATTTATTTA[C/T]TGTTTTTATGCAGGC	154214
rs9375379	snp	C/G	0.364817	0.222075	intron-variant	RNF217	GRCh38.p7	6:124980029	TGCTAGGTTTTACAA[C/G]TCTGTGTATCAGCTG	154214
rs9375381	snp	A/G	0.0142736	0.0832652	intron-variant	RNF217	GRCh38.p7	6:124997818	GCTTTTCTAGACTCT[A/G]CTAACTTAATGTATT	154214
rs9375382	snp	C/G	0.484421	0.0868729	intron-variant	RNF217	GRCh38.p7	6:124998069	TATGTTCAGAGCAAA[C/G]TTTTAATATTTCTTC	154214
rs9375383	snp	A/C	0.496348	0.0425753	intron-variant	RNF217	GRCh38.p7	6:125033008	ttgtacttttccctg[A/C]tgacttatgaagttg	154214
rs9375384	snp	A/C	0.494976	0.0498674	intron-variant	RNF217	GRCh38.p7	6:125034915	AGAGGTCCTTCACAT[A/C]CCTTGTAAGTTGGAT	154214
rs9375385	snp	C/T	0.492871	0.0592773	intron-variant	RNF217	GRCh38.p7	6:125040267	atggggatatcacca[C/T]ggatcccacagcaat	154214
rs9375386	snp	A/G	0.398714	0.200958	intron-variant	RNF217	GRCh38.p7	6:125047328	ACAATTATGGCAATA[A/G]TGAAATGTTTTACGT	154214
rs9375387	snp	C/T	0.0295035	0.117819	intron-variant	RNF217	GRCh38.p7	6:125070462	taacttgcagttcca[C/T]aaacataaaagtgtt	154214
rs9385360	snp	C/T	0.293294	0.246223	intron-variant	RNF217	GRCh38.p7	6:124994368	TTCAGTATGTATCTC[C/T]CTAAAGTGAGGACTT	154214
rs9385361	snp	G/T	0.115392	0.210667	intron-variant	RNF217	GRCh38.p7	6:125019833	TCCCCTTTTTTGCAG[G/T]GGGGGGGGAGTGAAA	154214
rs9385362	snp	A/G	0.453331	0.145452	intron-variant	RNF217	GRCh38.p7	6:125064324	TTTATGGTATGCCAA[A/G]CTCTAGACCTTAGTT	154214
rs9385363	snp	C/G	0.488302	0.0755777	intron-variant	RNF217	GRCh38.p7	6:125065317	AAAAAAAAAGTCATG[C/G]AAATGTTATTTTGTG	154214
rs9388395	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124985809	AAGGTTGTACTTTTT[A/G]TATAAAAAACCAGGA	154214
rs9388396	snp	A/G	0.376394	0.215696	intron-variant	RNF217	GRCh38.p7	6:124994376	GTATCTCCCTAAAGT[A/G]AGGACTTATTCTTTT	154214
rs9388397	snp	A/G	0.390651	0.206682	intron-variant	RNF217	GRCh38.p7	6:125003258	ATCGAGAGGCTGTAT[A/G]GTTGTACAATCACTG	154214
rs9388398	snp	A/G	0.497881	0.0324789	intron-variant	RNF217	GRCh38.p7	6:125011665	TTTATATGAGAGAGC[A/G]AGGAGTGTCAGGTTC	154214
rs9388399	snp	C/T	0.396909	0.202282	intron-variant	RNF217	GRCh38.p7	6:125012651	TTTGTTCCTATGTTT[C/T]CCTTTGGTGCTCCTT	154214
rs9388400	snp	C/T	0.268995	0.249277	intron-variant	RNF217	GRCh38.p7	6:125019503	tatatatgttattct[C/T]atatgactattacat	154214
rs9388401	snp	A/G	0.34659	0.230587	intron-variant	RNF217	GRCh38.p7	6:125027911	gacatcagtgatgtt[A/G]agcatcttttcatat	154214
rs9388402	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125031194	gtgggcccagcccac[G/T]aaaccactttttcct	154214
rs9388403	snp	G/T	0.0252325	0.109451	intron-variant	RNF217	GRCh38.p7	6:125038547	GTAAGCTAGAGGATG[G/T]CTATTTAAGGATTCA	154214
rs9388404	snp	C/T	0.473634	0.111748	intron-variant	RNF217	GRCh38.p7	6:125074000	TTCAAACACAGGGCT[C/T]TGTGAAGTCAAAGCT	154214
rs9388405	snp	G/T	0.0023933	0.0345097	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087347	ACCTGCACATAAGCC[G/T]TAATGTGAGTCTTCA	154214
rs9398772	snp	C/T	0.00716266	0.059414	intron-variant	RNF217	GRCh38.p7	6:125044044	TAGCAATGTTAAAAG[C/T]TACTATGAATTTAGT	154214
rs9398773	snp	A/C	0.472522	0.113946	intron-variant	RNF217	GRCh38.p7	6:125073676	ACTTGCCTATCTAGG[A/C]AAGCACTCTCTAGTC	154214
rs9401790	snp	C/T	0.257141	0.249898	missense, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963311	TAGGGGATCCCTATG[C/T]GCCCCTCATGGTGCT	154214
rs9401791	snp	A/C	0.356169	0.226336	intron-variant	RNF217	GRCh38.p7	6:124987066	actagcatgtatgca[A/C]attcataatttggac	154214
rs9401792	snp	C/G	0.392881	0.205147	intron-variant	RNF217	GRCh38.p7	6:125003719	TATATAATTATTTGT[C/G]AATTTTAAAAATACA	154214
rs9401793	snp	A/C	0.0267878	0.112589	intron-variant	RNF217	GRCh38.p7	6:125004955	TTATGGTTCTGGAGG[A/C]TGGGAAGTCCAAGTG	154214
rs9401794	snp	C/T	0.302184	0.244493	intron-variant	RNF217	GRCh38.p7	6:125019445	tctacatttagaata[C/T]tgtgactatataagc	154214
rs9401795	snp	A/G	0.269267	0.249256	intron-variant	RNF217	GRCh38.p7	6:125021565	CCACTGCACCCGGCC[A/G]GAAAATGCTTACCTT	154214
rs9401798	snp	C/T	0.495252	0.0484902	intron-variant	RNF217	GRCh38.p7	6:125033221	tttttatacttaagt[C/T]ttagggtacatgtgc	154214
rs9401799	snp	G/T	0.495634	0.0465208	intron-variant	RNF217	GRCh38.p7	6:125034645	GATGCCTCCAGCTTT[G/T]TTCTTTTGGCTTAGG	154214
rs9401800	snp	G/T	0.417196	0.185864	intron-variant	RNF217	GRCh38.p7	6:125044486	TTGCGTTTTGATGTA[G/T]CCTCCCTTCTCTCCT	154214
rs9401802	snp	A/G	0.189261	0.242509	intron-variant	RNF217	GRCh38.p7	6:125061552	TATTTAGATATTTAA[A/G]CTCCACTTCTGGCAT	154214
rs9401803	snp	G/T	0.147656	0.228091	intron-variant	RNF217	GRCh38.p7	6:125072041	AACCTATGTTTTAAG[G/T]CTTTGTGTTTTAAAA	154214
rs9401804	snp	C/T	0.00478085	0.0486577	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085453	AATTTTTTACTAAGT[C/T]TCATCAAGATCTTAA	154214
rs9482581	snp	A/T	0.370162	0.219229	intron-variant	RNF217	GRCh38.p7	6:124992903	CTAAAACGATTTATG[A/T]CTTTGATGATGTTAC	154214
rs9482582	snp	G/T	0.366679	0.221102	intron-variant	RNF217	GRCh38.p7	6:124993404	TTCCACTAAAATTAT[G/T]ATCATTAGCCCATCT	154214
rs9482583	snp	C/T	0.359787	0.224604	intron-variant	RNF217	GRCh38.p7	6:124997233	ctatagaagagttca[C/T]ggctccatgtatttg	154214
rs9482584	snp	A/C	0	0	intron-variant	RNF217	GRCh38.p7	6:124998650	ctaaaaatacaaaaa[A/C]cctagtgaagcatgg	154214
rs9482586	snp	A/G	0.0437281	0.141251	intron-variant	RNF217	GRCh38.p7	6:125036432	tttataatcctttgg[A/G]tatatacccagtaat	154214
rs9482588	snp	A/G	0.0260105	0.111035	intron-variant	RNF217	GRCh38.p7	6:125050517	ATAAACACTACACAA[A/G]TATTTTCTCATGTGG	154214
rs9482590	snp	C/T	0.126909	0.217598	intron-variant	RNF217	GRCh38.p7	6:125063442	TTCTGGATTCTGATA[C/T]GCCATCTCTATACAA	154214
rs9482591	snp	C/T	0.0916144	0.193427	intron-variant	RNF217	GRCh38.p7	6:125066727	AACATATTTTGCAGC[C/T]GTGAGAGCAGAGATT	154214
rs9482592	snp	A/G	0.0240643	0.107019	intron-variant	RNF217	GRCh38.p7	6:125077456	TGAAAATGCTTTTGT[A/G]GATTGACTTTTTACC	154214
rs9482593	snp	A/G	0.151668	0.229849	intron-variant	RNF217	GRCh38.p7	6:125078824	TTTTCCCCACCCCAA[A/G]CACAGCTGCCTCTTA	154214
rs9482594	snp	A/G	0.152001	0.229992	intron-variant	RNF217	GRCh38.p7	6:125079141	CCACGTGCTCAGCTA[A/G]AGATCAGAGGTTCTG	154214
rs9482595	snp	A/G	0.0225045	0.103662	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084085	TATCCTAACCTTGTT[A/G]TCTCTTGCCTCCTCC	154214
rs9491273	snp	C/G	0.0387552	0.1337	intron-variant	RNF217	GRCh38.p7	6:124991248	gctcactcagaacca[C/G]cttctcggactcttt	154214
rs9491274	snp	A/G	0.372189	0.218105	intron-variant	RNF217	GRCh38.p7	6:124998837	ATTTTGTCAACATAA[A/G]ATTATAAGCACCTGT	154214
rs9491275	snp	C/G	0.389152	0.207694	intron-variant	RNF217	GRCh38.p7	6:125002482	CTTAGAGAATTGCTT[C/G]CTTCTCTATGCTTTG	154214
rs9491277	snp	C/T	0.367297	0.220775	intron-variant	RNF217	GRCh38.p7	6:125008131	CCTGGTGGCAGGCAC[C/T]TATAGTCCCAGCTAC	154214
rs9491279	snp	C/T	0	0	intron-variant	RNF217	GRCh38.p7	6:125012279	AGCACAACAGAATGA[C/T]TATGTTTCAGTTTGA	154214
rs9491280	snp	G/T	0.493201	0.0579089	intron-variant	RNF217	GRCh38.p7	6:125025666	AAGGAAGGGAGGGAG[G/T]GAGGAAAGAAGGGAG	154214
rs9491282	snp	C/T	0.390277	0.206936	intron-variant	RNF217	GRCh38.p7	6:125034513	atagttgtagatatg[C/T]gacattatttctgag	154214
rs9491283	snp	C/G	0.0670745	0.170406	intron-variant	RNF217	GRCh38.p7	6:125037767	TTGTGATTATTGTTA[C/G]TGCTTTCGTTGCAAT	154214
rs9491285	snp	C/T	0.0437281	0.141251	intron-variant	RNF217	GRCh38.p7	6:125043056	TCCAGACTCCTAAGA[C/T]GGCTTCATGCTCTGC	154214
rs9491286	snp	A/G			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045488	AGATGTCACATGGCA[A/G]AAGCAGCCAGATTAG	154214
rs9491287	snp	C/T	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:125047610	ATTCCTTTTGATTAG[C/T]AGAGGAAAAGAAAAT	154214
rs9491289	snp	A/G	0.02016	0.0983543	intron-variant	RNF217	GRCh38.p7	6:125054603	CAACAATGAGCACCC[A/G]TGCTACACAAAGCTC	154214
rs9491290	snp	A/G	0.0252325	0.109451	intron-variant	RNF217	GRCh38.p7	6:125054958	CCATGTGGTGGGTAT[A/G]TGGTTGTGAGATAGC	154214
rs9491291	snp	C/T	0.0252325	0.109451	intron-variant	RNF217	GRCh38.p7	6:125057040	ACTATATTGATATAT[C/T]TCTAATAATAGAATG	154214
rs9491292	snp	A/T	0.12932	0.218944	intron-variant	RNF217	GRCh38.p7	6:125061525	TTTTATTATCAAATT[A/T]TATGAGCTCTTTATT	154214
rs9491293	snp	A/G/T	0.127944	0.218179	intron-variant	RNF217	GRCh38.p7	6:125061629	GAGTGGTAGGTTTTC[A/G/T]TTTTTTTTTAAATTA	154214
rs9491294	snp	G/T	0.132409	0.220618	intron-variant	RNF217	GRCh38.p7	6:125062891	TCTTAATGCAAAGTA[G/T]TTTTCAGTCACTTAT	154214
rs9491295	snp	C/T	0.0803491	0.183626	intron-variant	RNF217	GRCh38.p7	6:125063073	AAGTCTAGTTCGTAA[C/T]AGTTTTAATATTAAA	154214
rs9491296	snp	C/G	0.131723	0.220251	intron-variant	RNF217	GRCh38.p7	6:125064931	ATAAAGTAGAATTAG[C/G]ttctgaatataacca	154214
rs9491297	snp	A/G	0.131723	0.220251	intron-variant	RNF217	GRCh38.p7	6:125065580	gttgagagcTGTGTT[A/G]TAGATGATGAGGGCT	154214
rs9491299	snp	A/C	0.0908922	0.192833	intron-variant	RNF217	GRCh38.p7	6:125068153	ATGAAAAAGAAGTAC[A/C]TGATCTGGGCCCCTG	154214
rs9491300	snp	A/C	0.164546	0.234942	intron-variant	RNF217	GRCh38.p7	6:125069538	tatataccacatttt[A/C]tttatccagtccact	154214
rs9491301	snp	A/G	0.157642	0.232314	intron-variant	RNF217	GRCh38.p7	6:125069922	tgggtaaattcttta[A/G]tggtgatttctgaga	154214
rs9491302	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125070238	tatatagcatgtttt[C/T]tttatccactcattg	154214
rs9491303	snp	G/T	0.0821764	0.185298	intron-variant	RNF217	GRCh38.p7	6:125074388	GAGAGGTGTTATCTT[G/T]TAAGTGACATTTTTG	154214
rs9491304	snp	C/T	0.15665	0.231917	intron-variant	RNF217	GRCh38.p7	6:125077556	ATAGAAACACAGACA[C/T]CTGCCCATAAACAAA	154214
rs9491305	snp	A/G	0.0279526	0.114869	intron-variant	RNF217	GRCh38.p7	6:125077621	GCAGGGTTCTTCGGC[A/G]GAATATTTCTTCTTC	154214
rs9491306	snp	C/T	0.0283406	0.115616	intron-variant	RNF217	GRCh38.p7	6:125078713	GGCCTGTCTTTTGTG[C/T]GTGCAGGCGCATGTG	154214
rs9491307	snp	C/T	0.00478085	0.0486577	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087652	GTCATCTCTTTAAAT[C/T]TGGGAGGAATCAGAA	154214
rs10080977	snp	A/G	0.362313	0.223351	intron-variant	RNF217	GRCh38.p7	6:125010878	AGCCCTCCCAGGTCT[A/G]CCACGGTACCTAAAA	154214
rs10214719	snp	A/G	0.0818113	0.184966	intron-variant	RNF217	GRCh38.p7	6:125062513	AAAACATAACCCACC[A/G]CATTAAGGTCAACTT	154214
rs10223681	snp	G/T	0.029116	0.117091	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087899	TCACTAAAAATATGA[G/T]CAATCAAAACTACCA	154214
rs10485341	snp	C/T	0.486984	0.079614	intron-variant	RNF217	GRCh38.p7	6:125075847	ATAATCAAGACTTTA[C/T]TCTTTGCGATAAAAT	154214
rs10485342	snp	C/T	0.124144	0.21601	intron-variant	RNF217	GRCh38.p7	6:125074198	ACAGCATATTACAGG[C/T]GGGCACTTCATACAT	154214
rs10485343	snp	C/T	0.173643	0.238054	intron-variant	RNF217	GRCh38.p7	6:125050155	AATAAGAATGAAACC[C/T]AGAATTGCACCTACC	154214
rs10485344	snp	A/G	0.0263992	0.111815	intron-variant	RNF217	GRCh38.p7	6:125026533	CACGTTTACGCTCTC[A/G]ATGCTCTAAAGGCTT	154214
rs10485345	snp	A/G	0.153332	0.230554	intron-variant	RNF217	GRCh38.p7	6:125001201	ATTCAGCATTCCCTA[A/G]TATAACTAACTCCAA	154214
rs10596029	in-del	-/AACAA			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961230	GGAGAAAAAAAACAA[-/AACAA]GGGCTGGCTTCCCAA	154214
rs10711866	in-del	-/T	0.14933	0.228835	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124960669	GCTGTGGGAATATAC[-/T]TTTTGGCATCCATTA	154214
rs10872293	snp	C/T	0.455502	0.142369	intron-variant	RNF217	GRCh38.p7	6:125061792	TATATCTTTTGTAAA[C/T]ATGTTGCTTCTGAGT	154214
rs11154282	snp	A/G	0.38286	0.211774	intron-variant	RNF217	GRCh38.p7	6:125011830	TATCTACTTTGATCA[A/G]CTGTGATGTTCAAAG	154214
rs11154283	snp	A/T	0.490119	0.0695896	intron-variant	RNF217	GRCh38.p7	6:125017165	AAAACTTTTTATGAC[A/T]CTGCCTTTCAATATG	154214
rs11154284	snp	C/T	0.496905	0.0392151	intron-variant	RNF217	GRCh38.p7	6:125017207	TAGTCATATGAATTT[C/T]CTTAGAATTTTATGC	154214
rs11154285	snp	C/T	0.307423	0.243316	intron-variant	RNF217	GRCh38.p7	6:125017418	GGCAGCTGTTCCTTC[C/T]CCATCTTTGGTAGCT	154214
rs11154287	snp	C/T	0.397813	0.201621	intron-variant	RNF217	GRCh38.p7	6:125031086	caccctctgaagcca[C/T]agcccgagctgtatg	154214
rs11154288	snp	C/T	0.317692	0.240661	intron-variant	RNF217	GRCh38.p7	6:125049706	TTATGATTGTTATTA[C/T]TATTAGGCAAAGAGA	154214
rs11154289	snp	A/G	0.381697	0.212499	intron-variant	RNF217	GRCh38.p7	6:125057769	ATCCTTGCCAAAGCA[A/G]TTCTTTCCTGTAGTA	154214
rs11154290	snp	A/G	0.369346	0.219673	intron-variant	RNF217	GRCh38.p7	6:125062000	ACTTTCCCCTCATCA[A/G]TTGATTTGTAATTTC	154214
rs11154291	snp	C/T	0.0916144	0.193427	intron-variant	RNF217	GRCh38.p7	6:125067783	GTAGAGATAAAGATC[C/T]ACCTTTGTTGGAATA	154214
rs11389498	in-del	-/C/G			intron-variant	RNF217	GRCh38.p7	6:125066997	GTGGAATGTTGCAGG[-/C/G]AGTATTATACGAGGG	154214
rs11413849	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124984549	CCTTTCTCAAAAAAA[A/T]AAAAAAAAAAAAGAA	154214
rs11451710	in-del	-/T	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125004064	GGTTACAGTTTTTTT[-/T]CTTTAAAATTCATCC	154214
rs11751039	snp	C/G	0.472896	0.113214	intron-variant	RNF217	GRCh38.p7	6:125067054	CTTGAGGAATCCAAG[C/G]GAGCTAGGTTGTGGA	154214
rs11751639	snp	A/C	0.0185938	0.0946107	intron-variant	RNF217	GRCh38.p7	6:125037904	CATGACCAACACTTA[A/C]AACCATGATCAGAGT	154214
rs11753660	snp	C/T	0.368938	0.219895	intron-variant	RNF217	GRCh38.p7	6:125011030	TGACTCTTTAGATTT[C/T]TTACATCACTTTGGA	154214
rs11754154	snp	A/G	0.403684	0.197183	intron-variant	RNF217	GRCh38.p7	6:125047134	TAATTCCATAAATTA[A/G]GATATTCAATTTTTT	154214
rs11754841	snp	C/T	0.418974	0.184249	intron-variant	RNF217	GRCh38.p7	6:124979133	TTTCAGGCTTCAGGC[C/T]GTCTTGGCTTGAAGG	154214
rs11758382	snp	G/T	0	0	intron-variant	RNF217	GRCh38.p7	6:124994977	AGGCTACTAATATTG[G/T]GTAAAAATGGGATGT	154214
rs11962762	snp	A/G	0.0166325	0.0896639	intron-variant, upstream-variant-2KB, missense	RNF217, RNF217-AS1	GRCh38.p7	6:124963785	AACTAACAAGCAGTG[A/G]GCATAGAATAAATAT	154214
rs11965842	snp	G/T	0	0	intron-variant	RNF217	GRCh38.p7	6:125013660	TAGCACAGTAAAAGA[G/T]AAGTATGTGAATTCT	154214
rs11969178	snp	C/G	0.0614824	0.164198	intron-variant	RNF217	GRCh38.p7	6:125054414	AATCAGACACAAGCT[C/G]TGGTAGTGTGAGAGC	154214
rs12110319	snp	C/T	0.109814	0.206997	intron-variant	RNF217	GRCh38.p7	6:125057821	GTAGTTTGAGTCTTA[C/T]AGAGGGGGAGGTATT	154214
rs12175234	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125033352	ctcccccctcccccc[A/C]ccccacaacagtccc	154214
rs12192918	snp	A/G	0.494526	0.0520291	intron-variant	RNF217	GRCh38.p7	6:125020984	CAAGTTGTAATTACT[A/G]TCATGGAACGTAAAT	154214
rs12194694	snp	A/G	0.00673393	0.0576335	intron-variant, upstream-variant-2KB, missense	RNF217, RNF217-AS1	GRCh38.p7	6:124963898	ATTCCAGGAAAGAGT[A/G]AATGTTTAAAAAAAT	154214
rs12195736	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125010231	ATACTGGGCTGCTCA[A/G]TGTGACTGGTAATTA	154214
rs12197409	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125032063	atctcgtgagactta[C/T]tcattatcacaagaa	154214
rs12203925	snp	G/T	0.0271762	0.113356	intron-variant	RNF217	GRCh38.p7	6:124994762	TATATTTCCAACTAT[G/T]CTTTCATCTTTTTTA	154214
rs12204645	snp	A/G	0.494484	0.0522255	intron-variant	RNF217	GRCh38.p7	6:125020193	CAGATGTCTGCCAAG[A/G]TCTTGATTATTCTAT	154214
rs12207846	snp	G/T	0.376791	0.215463	intron-variant	RNF217	GRCh38.p7	6:124997026	actcctgcaagttta[G/T]gttctacaaacacgg	154214
rs12211389	snp	C/G	0.380138	0.213458	intron-variant	RNF217	GRCh38.p7	6:124998797	AGCGAGACTCTGTCT[C/G]AAAAAACAAAAATTG	154214
rs12212692	snp	A/C			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981861	gtctctactaaaaat[A/C]caaaaaaaaaaaaaa	154214
rs12213635	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125000294	TAACATGAATTATTA[C/T]TTAAAAATTTGTCTT	154214
rs12523681	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125074247	TTCTTCAAAATGATC[A/T]CAGTCACCAAGAAAC	154214
rs12660986	snp	A/G	0.145642	0.227177	intron-variant	RNF217	GRCh38.p7	6:124968733	GATTTTTCCCTCCTA[A/G]AGCTTTTATACCTGA	154214
rs12664303	snp	C/T	0.397813	0.201621	intron-variant	RNF217	GRCh38.p7	6:125048528	CCTTGTAATGTTTAT[C/T]TTAATGTTATTCTGA	154214
rs13196351	snp	C/G	0.154661	0.231107	intron-variant	RNF217	GRCh38.p7	6:125025521	CTTTCTACCGAGGAG[C/G]GAGGGAGGAAGGGAT	154214
rs13197518	snp	G/T			missense, intron-variant, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962786	CGGGCTGGAGTAAGA[G/T]CCGAGCACCGGCGCA	154214
rs13197636	snp	G/T			stop-gained, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962869	CAGTTGGAGCTGGAG[G/T]AGGAAGAGGAGGAAG	154214
rs13197637	snp	A/G/T	1.81092e-05	0.00300903	missense, stop-gained, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962872	TTGGAGCTGGAGGAG[A/G/T]AAGAGGAGGAAGCTG	154214
rs13197804	snp	C/T	0.355311	0.226737	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981689	tacgctatcatatat[C/T]gccagggtgaaaatc	154214
rs13200005	snp	C/T	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125033505	caatttcatccatgt[C/T]cctacaaaggacatg	154214
rs13200116	snp	C/T	0.419456	0.183806	intron-variant	RNF217	GRCh38.p7	6:125033571	ggtgtatatgtgcca[C/T]attttcttaatccag	154214
rs13201990	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125035438	caacccagaatttca[A/T]atccagccaaactaa	154214
rs13205778	snp	A/T	0.244205	0.249933	intron-variant	RNF217	GRCh38.p7	6:124998412	TAAATCTGTCTGCTT[A/T]TCTCCATCTTCACTT	154214
rs13209472	snp	A/G	0.378765	0.214288	intron-variant	RNF217	GRCh38.p7	6:124998901	TTCTCACTTTGGTCC[A/G]GAACAATGCCTTACA	154214
rs17052573	snp	A/G	0.407674	0.194008	intron-variant	RNF217	GRCh38.p7	6:124985668	GAATTTTAAGGACAC[A/G]TAAAGCCACAATATA	154214
rs17052599	snp	C/G	0.152667	0.230274	intron-variant	RNF217	GRCh38.p7	6:125011858	AAGAAACTCTTCTCG[C/G]TGAGATAATAACTGC	154214
rs17052615	snp	A/G	0.155987	0.23165	intron-variant	RNF217	GRCh38.p7	6:125014266	GAGATTTTGGAAATA[A/G]TGATAGCAATCACTC	154214
rs17052665	snp	G/T	0.0364509	0.129988	intron-variant	RNF217	GRCh38.p7	6:125053210	TTGTCCCAGCTTCTA[G/T]TCTGGCAGTTACTAT	154214
rs17052705	snp	A/G	0.00597247	0.0543191	intron-variant	RNF217	GRCh38.p7	6:125077409	GTATCAAATGCCCTC[A/G]GTGCATACAAACCCA	154214
rs17052714	snp	C/G	0.00636936	0.0560724	intron-variant	RNF217	GRCh38.p7	6:125080686	GGGATTCTGATGTTG[C/G]ACTCTGCTATGTATA	154214
rs17052719	snp	A/G	0.0287284	0.116357	intron-variant	RNF217	GRCh38.p7	6:125082320	AATAAAATGATTTTC[A/G]TATGTCAACTTGGGT	154214
rs17720559	snp	A/G	0.368119	0.220336	intron-variant	RNF217	GRCh38.p7	6:124966415	TGAACCACATCAAAA[A/G]GGCATAGTGAGTGCT	154214
rs17722237	snp	A/G	0.396546	0.202545	intron-variant	RNF217	GRCh38.p7	6:125045955	GCTTCAAAAAAAGTC[A/G]AAGATGGGAGAGACA	154214
rs17779477	snp	C/G	0.151334	0.229706	intron-variant	RNF217	GRCh38.p7	6:125080355	GTATACATGTCTGGT[C/G]ATCTGGTTCCAAAGA	154214
rs17779663	snp	C/T	0.00801747	0.0628049	intron-variant	RNF217	GRCh38.p7	6:125082594	TGCAAATGATATGAC[C/T]GTGGACAATAAAGAA	154214
rs28360578	snp	A/G	0.143959	0.226396	intron-variant	RNF217	GRCh38.p7	6:125021748	TTCCTTTATAAAGTC[A/G]TTTATCAGCTGTACA	154214
rs28374785	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125033351	CCTCCCCCCTCCCCC[C/G/T]ACCCCACAACAGTCC	154214
rs28496521	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125063855	TTATTCATAATTTAT[G/T]ATAAATTTGGAATTA	154214
rs28547569	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125046141	GAGCATTTCAGAGCA[A/G]GGGATGAGTAAGTGC	154214
rs28612472	snp	A/G	0.367503	0.220665	intron-variant	RNF217	GRCh38.p7	6:125007979	AAAATTTATGTGGCC[A/G]GGCCTGGTGGCTCAT	154214
rs28616026	snp	A/T	0.367503	0.220665	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125007059	ATAAAGTTCTAGACA[A/T]TTAATTCTGAGATTT	154214
rs28625936	snp	A/G	0.367297	0.220775	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125007062	AAGTTCTAGACAATT[A/G]ATTCTGAGATTTGTT	154214
rs28700225	snp	C/G	0.368529	0.220116	intron-variant	RNF217	GRCh38.p7	6:124978313	TGCTCCACCTGCTTA[C/G]CCCGGCAGGCTGCAT	154214
rs28703312	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124975481	TGTTGCCTGGGCAGG[A/C]GTGCAGTGGCTCAAT	154214
rs28833574	snp	C/T	0.0126979	0.078662	intron-variant	RNF217	GRCh38.p7	6:125035104	GATTTTGGGCAGAGA[C/T]AATGGGGTTTTCTAG	154214
rs34048906	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:124979682	TAGTATAGATCCTCC[-/C]ATGGAAATTATACTT	154214
rs34053929	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:124988597	TGTTCACTAGCTTTT[-/T]AAATTTGTCAAACTA	154214
rs34181408	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125041450	ATAATACAGACTTTT[-/T]ACCATGGCCAACAAG	154214
rs34214742	in-del	-/G			intron-variant	RNF217	GRCh38.p7	6:125025083	GTCAGGAAAATCAGG[-/G]AATGTGATGTGCTAG	154214
rs34249175	in-del	-/A	0.419296	0.183954	intron-variant	RNF217	GRCh38.p7	6:125045144	AGTAATACTGTATAC[-/A]AAAAAAAAAATGAAA	154214
rs34254487	in-del	-/G			intron-variant	RNF217	GRCh38.p7	6:124995873	TTGCAGTGAGCCGAG[-/G]ATCGTGTCATTGCAC	154214
rs34267556	in-del	-/TT			intron-variant	RNF217	GRCh38.p7	6:125021269	TAACATGGAAAAAGC[-/TT]TTTTTTTTTTTTTTG	154214
rs34293295	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125044771	ATGTGCCCAGAGTTT[-/T]AGTGCTGAAGTATTC	154214
rs34301584	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:125061215	GGGTTAAAGAATACC[-/C]TAAGTTTTTAGTATT	154214
rs34412026	in-del	-/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088036	TTTTTTTTTTTTTTT[-/T]GAGACAGAGGTTCTC	154214
rs34458789	in-del	-/C			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982605	AACTTATAATCATTG[-/C]CCGTTTTATAGATCA	154214
rs34482928	in-del	-/G			intron-variant	RNF217	GRCh38.p7	6:124985472	CTCTTAGTTATTTTG[-/G]GAAGTGAATTTCTAT	154214
rs34493802	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:125077423	AGTGCATACAAACCC[-/C]AAGTTTAATTATCCA	154214
rs34549001	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:124965469	CCCAGCTACTTGGAA[-/A]GGCTGAGGCAGAAGA	154214
rs34561311	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:124993285	TTTTACAAGTATCTT[-/T]GGGTTTTCTGACTAA	154214
rs34583129	in-del	-/C			intron-variant, utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:124966818	CTGTGACAAAGGCCA[-/C]ATTGGTAGGTGTCAT	154214
rs34607926	snp	A/G	0.0329836	0.124112	intron-variant	RNF217	GRCh38.p7	6:125026918	TGTGTTTTGGATACA[A/G]TAAATATTAATATTA	154214
rs34627580	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:125015662	GGTATCGCTACATCC[-/C]AGTATATTTTCTCTA	154214
rs34689016	in-del	-/G			intron-variant	RNF217	GRCh38.p7	6:125023587	ATCTATATCTCAAGG[-/G]AAATGAAATTAGTAT	154214
rs34723320	in-del	-/T			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125083039	ACTGAGAGGAACCTT[-/T]CTACCATCTCATCTC	154214
rs34727287	snp	A/G	0.100231	0.200173	intron-variant	RNF217	GRCh38.p7	6:124993704	ACATAGGAAGGCCGG[A/G]TAGGCCAGCTGTTTG	154214
rs34759038	in-del	-/TT	0.0535932	0.154675	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086400	GCCTCATTTTAAAAC[-/TT]GAGGGATTTAAATCA	154214
rs34789030	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:125050719	TGTTCTGGTTTTCCC[-/C]TGACACCATCACTTT	154214
rs34860876	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125058571	ATTGTTTTGCTTTTT[-/T]GCAAATCTGGTAAAG	154214
rs34875299	in-del	-/G			intron-variant	RNF217	GRCh38.p7	6:125066361	CCCGTCGCCCTCTGG[-/G]ACATGTCCCCACTCT	154214
rs34876592	in-del	-/G			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982430	ATACTTTTTCAATAT[-/G]TTATCTCACTTTCCA	154214
rs34890554	in-del	-/T	0.499382	0.017561	intron-variant	RNF217	GRCh38.p7	6:125044059	TTACTATGAATTTAG[-/T]TTTTTTTTTTAATTG	154214
rs34909133	in-del	-/GAG			intron-variant	RNF217	GRCh38.p7	6:124988022	CAGGCCACATAGGAG[-/GAG]ATAATGCTCGGGTGA	154214
rs34927393	in-del	-/AA	0.4862	0.0819127	intron-variant	RNF217	GRCh38.p7	6:124997461	AGGTTCACACAACTC[-/AA]GAGTTAATATATTCC	154214
rs34965023	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125028634	GGAAAGAGCATAAAA[-/A]TAAAACTGGAAATAA	154214
rs35017427	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125074559	TAGGAACTTCAAAAA[-/A]CTTTTTATTCCTAAA	154214
rs35066049	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:124994300	CCCACTCACTTCCCC[-/C]TTCCCTTCCTTATTT	154214
rs35081305	in-del	-/A			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961899	CACACCCACTCAGGG[-/A]TGTGCGTGTGTGTGT	154214
rs35087333	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:125065948	TGTTCTCTTCTCCCC[-/C]AAAATGGTTCTTCTC	154214
rs35100819	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125073982	AGCTAGTGGAGCTAG[-/T]AATTCAAACACAGGG	154214
rs35109110	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125008784	TTCCTTCTCTTTGTT[-/T]CAAGCTTAATTAGGT	154214
rs35130441	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:124994659	CTACAACCTGCTTTT[-/T]GTATATATCCTCAAA	154214
rs35136006	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125044383	TTAATCATTTAAAAA[-/A]TTAGTTGTGTCCACA	154214
rs35148637	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125037300	GCTGTTGTATCAAAA[-/A]TACCAGAAACGGAGT	154214
rs35154807	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:124965679	GTACTTGGTTTTCCC[-/C]TGTTCCAGGAAGGTT	154214
rs35155385	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124996491	TCTACCAATTCATGG[G/T]TTTCTTTTTCTATTT	154214
rs35223447	in-del	-/T/TT	0.499663	0.0129749	intron-variant	RNF217	GRCh38.p7	6:125007249	CATTTTTTTTTTTTT[-/T/TT]GAGATGGAGTTTCCC	154214
rs35248447	snp	A/G	0.399432	0.200425	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086319	AGGAAATTTTTTTTC[A/G]ATAAAAATAAAATTT	154214
rs35294854	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124977282	GACACCAAAGTAAGT[A/T]TAATGATTTAGAAAG	154214
rs35310826	snp	G/T	0.155656	0.231515	intron-variant	RNF217	GRCh38.p7	6:125026353	TGGGATCCTGGTAGG[G/T]TCTTTATCAGGAGTA	154214
rs35322947	in-del	-/C			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084039	AATTATAGATAATTC[-/C]TGCTTTAGGTCAAGG	154214
rs35355221	snp	C/T	0.416545	0.186448	intron-variant	RNF217	GRCh38.p7	6:124976275	TCCCTCCCTCCCTCC[C/T]GCTCTCTCTCCTTTC	154214
rs35374262	in-del	-/C	0.0667028	0.170006	intron-variant	RNF217	GRCh38.p7	6:125053637	TTTGTGGGTTGTTTC[-/C]TTACTCGACTTGATG	154214
rs35377423	in-del	-/AG/GA	0	0	intron-variant	RNF217	GRCh38.p7	6:125072855	CATAATAAAGAAACA[-/AG/GA]CATGGATTCAAAATC	154214
rs35389094	in-del	-/G			intron-variant	RNF217	GRCh38.p7	6:125043877	ATACTTTTAACAGGT[-/G]CAATACTAATAAGGA	154214
rs35397980	snp	A/T	0.23031	0.249223	intron-variant	RNF217	GRCh38.p7	6:124978227	GGATTCCTTCTGTGC[A/T]GCTTCACCAGTCAGA	154214
rs35545666	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:125011774	AGTTCTTTACTTTTC[-/C]ATTGCATTTCACTTT	154214
rs35553840	in-del	-/G			intron-variant	RNF217	GRCh38.p7	6:124980302	CAATTTGCTTTTTTT[-/G]CAGTCTTTCGTTAAT	154214
rs35561609	in-del	-/T	0.376592	0.215579	intron-variant	RNF217	GRCh38.p7	6:124992178	TTTGAGTAGCAAGGC[-/T]GTAGAATGCTCTAAA	154214
rs35574496	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125080017	CTGTGATATTTGAGA[-/A]GGAAAAAGAAAATCA	154214
rs35606374	in-del	-/G			intron-variant	RNF217	GRCh38.p7	6:125010442	TACTGTAATTCTCTT[-/G]CTAAACAAGCAATTC	154214
rs35672227	in-del	-/A	0.351635	0.228408	intron-variant, upstream-variant-2KB, utr-variant-3-prime	RNF217, RNF217-AS1	GRCh38.p7	6:124964441	TCTGGACAATGTCTT[-/A]AGAGTCCCATATGTG	154214
rs35767917	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125041604	ACTGGAGCCAATGTT[-/T]CTTGTTTCCTTTGTT	154214
rs35831046	snp	G/T	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125060444	TTTTAGTAAATATTG[G/T]TATTTATTTATTTAT	154214
rs35859132	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124991297	CCCATGTCTGCATTA[A/G]GACCTTTCCAGTAGC	154214
rs35878374	in-del	-/G			intron-variant	RNF217	GRCh38.p7	6:125072478	GCCTGCTGCATTTGG[-/G]AATATAATAATACTA	154214
rs35878634	snp	A/G	0.473359	0.112298	intron-variant	RNF217	GRCh38.p7	6:125067001	GAATGTTGCAGGAGT[A/G]TTATACGAGGGTTCA	154214
rs35889719	in-del	-/G			intron-variant	RNF217	GRCh38.p7	6:124980208	ACATCTTTTGCGAAG[-/G]ATGTCCATAATTATT	154214
rs35946385	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125062756	TAATTTTTGTATTTT[-/T]AGTAGAGACGAGGTT	154214
rs35986204	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:125052594	AAAATATGTTTTCCC[-/C]ATATGGAGAATTTCT	154214
rs36008126	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:124987754	AGCTGGGACTATACC[-/C]TTGCCTGGCTCTTAT	154214
rs36014454	snp	C/T	0.030954	0.120494	synonymous-codon, nc-transcript-variant	RNF217	GRCh38.p7	6:125057980	CCAAGGAGAGTGGCA[C/T]TTAAAACACCAGACG	154214
rs36026279	snp	C/G	0.231189	0.249291	intron-variant	RNF217	GRCh38.p7	6:125008982	AAATGTGTTTCCCCT[C/G]GTTTAATGGTTGAAA	154214
rs36050144	in-del	-/G			intron-variant	RNF217	GRCh38.p7	6:125057829	AGTCTTATAGAGGGG[-/G]AGGTATTTTAAATTA	154214
rs36058992	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125018947	CCACATGTTCCAGCA[-/A]CTAACAGCTGGACAT	154214
rs36060063	snp	A/G	0.34437	0.231505	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124967858	ATCTTGGCTCACTGC[A/G]ACCTTTGCCTCCCGG	154214
rs36148957	in-del	-/T	0.311369	0.242351	intron-variant	RNF217	GRCh38.p7	6:125033449	GGTGTTTGGTTTTTT[-/T]GTCCTTGTGATAGTT	154214
rs36158552	snp	A/T	0.342134	0.232404	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961137	AACCCAATAACAACT[A/T]CGAGATTAAAAAATA	154214
rs41507346	snp	A/G	0.14933	0.228835	intron-variant	RNF217	GRCh38.p7	6:125025038	GTATCCTCCTTTGTG[A/G]ATTTTCCCTGCATCT	154214
rs41517847	snp	A/G	0.0341408	0.126114	intron-variant	RNF217	GRCh38.p7	6:125075781	TGTATAGAAATTAGA[A/G]CCATCTTTATCTGTG	154214
rs41523048	snp	C/T	0.151668	0.229849	intron-variant	RNF217	GRCh38.p7	6:125023367	GTTTTCACTTTATCC[C/T]GAACACAAGGGCATT	154214
rs55705569	in-del	-/T	0	0	intron-variant	RNF217	GRCh38.p7	6:125008756	TTTTTTTTTTTTTTT[-/T]AACCCTGTAGGTTTC	154214
rs55738637	snp	G/T	0.00358779	0.0422022	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125083597	AGGCCCAGTAACCTT[G/T]TACTTACCCAGTTCC	154214
rs55924553	snp	A/G	1.64879e-05	0.00287118	intron-variant, utr-variant-5-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125009228	AATCAAAGCTGTTGT[A/G]TAATTAGTTCTCTTC	154214
rs55937562	snp	A/G	0.00597247	0.0543191	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125083539	CTGAAGTGTATATGC[A/G]TAGGGGCGTGAATGT	154214
rs56007458	snp	A/C	0.0341408	0.126114	intron-variant	RNF217	GRCh38.p7	6:125074533	ACTGAAATACTGCAC[A/C]TAATTTGGAGTTAGG	154214
rs56048457	snp	G/T	0.40595	0.195396	intron-variant	RNF217	GRCh38.p7	6:124966194	TAGCCTTTTTTAGTT[G/T]GTTAAAAATACAGGA	154214
rs56189963	snp	C/T	0.0119091	0.0762411	intron-variant	RNF217	GRCh38.p7	6:124998893	GGAATCTATTCTCAC[C/T]TTGGTCCAGAACAAT	154214
rs56294755	in-del	-/GTTTGA	0	0	intron-variant	RNF217	GRCh38.p7	6:124989642	AACACTTAAATTTGA[-/GTTTGA]TATAATTTTCATGTT	154214
rs56298622	snp	A/T	0.0325976	0.123435	intron-variant	RNF217	GRCh38.p7	6:124988794	CCACAGAGAATGTTC[A/T]TTCATAGAGACTGAT	154214
rs56367046	snp	C/T	0.00291102	0.03804	intron-variant	RNF217	GRCh38.p7	6:125082816	TTTAAAATAGGAAAA[C/T]CTAAATGCCTCTCAT	154214
rs56400684	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125037245	GGCAGAAAAAGTTTT[A/C]CAACTTTATTTTTCT	154214
rs56411912	snp	A/G	0.155656	0.231515	intron-variant	RNF217	GRCh38.p7	6:125012064	AGCCTTAGATTAAAT[A/G]AAAGAGATAGTCAGA	154214
rs57155603	snp	C/T	0.0479149	0.147179	intron-variant	RNF217	GRCh38.p7	6:125022139	CACCTACCTTGGCCT[C/T]CCAAAGTGCTGGGAT	154214
rs57288886	snp	A/G	0.0267878	0.112589	intron-variant	RNF217	GRCh38.p7	6:124976444	CAGCTAATTTTTTGT[A/G]TTTTTAGTAGAGATG	154214
rs57503125	in-del	-/TAACA			intron-variant	RNF217	GRCh38.p7	6:125063684	ACAATAATTATAACA[-/TAACA]GGATTGGTAGTATGT	154214
rs57724575	snp	C/G	0.0349115	0.127424	intron-variant	RNF217	GRCh38.p7	6:125066158	CTAACCTGGGGCAAG[C/G]CATCATCGTCTTTCT	154214
rs57903248	snp	C/T	0.0599851	0.162463	intron-variant	RNF217	GRCh38.p7	6:124981207	TTATGTTTAAAACAG[C/T]CATTAAATTTGTAAT	154214
rs58240474	in-del	-/T	0.0349115	0.127424	intron-variant	RNF217	GRCh38.p7	6:125001890	TGTTACTCCCATCAA[-/T]TTATTCCCTGACAGA	154214
rs58375751	snp	C/T	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125053824	TAAGATTCTTAGCTC[C/T]GATAACTTTATTCTT	154214
rs58658025	snp	A/G	0.188946	0.24243	intron-variant	RNF217	GRCh38.p7	6:125055694	CAATAGAAGATAACC[A/G]AATTAACTTTTCAGG	154214
rs58793551	in-del	-/TTAC			intron-variant	RNF217	GRCh38.p7	6:125062424	GATCAAGATACTTAC[-/TTAC]AAGTATGATTTTTAT	154214
rs58808898	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124985631	GATCAAGTTTCAGAA[A/T]TAAAGCAGTTTCAAA	154214
rs58944874	snp	A/T	0.153332	0.230554	intron-variant	RNF217	GRCh38.p7	6:125001456	ATTAATGTTACCACC[A/T]GTCTTATAACATGGC	154214
rs59219100	snp	G/T	0.0142736	0.0832652	intron-variant	RNF217	GRCh38.p7	6:124976384	AGCAATTCTCCTGCC[G/T]CAGCCTCCTGAGTAG	154214
rs59344673	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125003495	CATCATTATCATCAT[C/G]GTCATCCAAAGATGA	154214
rs59462089	in-del	-/AT			intron-variant	RNF217	GRCh38.p7	6:125013351	TTGCATGTTTTGTGT[-/AT]GTGTGTGTGTGTGTG	154214
rs59775061	in-del	-/ACACATATAAATTACTTAGCACCACATAT	0.153665	0.230694	intron-variant	RNF217	GRCh38.p7	6:125049644	GAATTAAATGAAATC[lengthTooLong]GACACATACTGGAAA	154214
rs59911756	snp	A/C	0.406814	0.194704	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982307	GTTTGCAAGAAGTTT[A/C]TCTGTAAATGTGATG	154214
rs59923339	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090019	TCAGCTGACAAGAAA[C/T]CCTTCTAAGACCCAT	154214
rs59977474	in-del	-/GGGA			intron-variant	RNF217	GRCh38.p7	6:125025775	GGAGGGAGGGAGGGA[-/GGGA]AGGAAGGAAGGAAGG	154214
rs60220443	snp	C/T	0.0391387	0.134304	intron-variant	RNF217	GRCh38.p7	6:125001655	TCCAGAGTTCACACA[C/T]TTGTCTTGGTCTTTC	154214
rs60384087	in-del	-/A			downstream-variant-500B	RNF217	GRCh38.p7	6:125092680	TTAAAAAATTAAAAA[-/A]TAAAACTTCACAGCA	154214
rs60399881	snp	A/G	0.0414363	0.137845	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087306	TGTATGCCAAAAAAC[A/G]TTTTTAGATTTTAAT	154214
rs60591491	snp	A/C	0.0611083	0.163768	intron-variant	RNF217	GRCh38.p7	6:124981135	AAGAATACTGTTTAT[A/C]ATGTTTGTGAAAAAA	154214
rs60695660	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125013519	AGAAGGTCAAGCAGG[C/T]ACCACAGCCCTGAGG	154214
rs61208735	in-del	-/ATAG			intron-variant	RNF217	GRCh38.p7	6:125074352	TAGATAGATAGATAG[-/ATAG]GGATGGGAGGAAGGG	154214
rs61361981	snp	A/G	0.232943	0.249417	intron-variant	RNF217	GRCh38.p7	6:125027781	CACCAAAAGTGTACA[A/G]AGGTTCCCTTTTCTC	154214
rs61446997	in-del	-/GATAAGG			intron-variant, upstream-variant-2KB	RNF217-AS1, RNF217	GRCh38.p7	6:124960540	ACCTAAGGGATAAGG[-/GATAAGG]AATAAAATGGTAAAC	154214
rs61496685	in-del	-/GTGTGTGT			intron-variant	RNF217	GRCh38.p7	6:125071530	TGTGTGTGTGTGTGT[-/GTGTGTGT]ATATCTTATTACAGG	154214
rs61622422	in-del	-/GG			intron-variant	RNF217	GRCh38.p7	6:125019841	TTGCAGTGGGGGGGG[-/GG]AGTGAAAAAATCCTT	154214
rs62431248	snp	C/G	0.5	0	intron-variant	RNF217	GRCh38.p7	6:124969739	TGGAATTATATGCTA[C/G]GCTGTGGAAATGGAA	154214
rs62431249	snp	A/G	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:124971327	ATGTTTTGAGGAAGC[A/G]AAAGGCTGCCACTCA	154214
rs62431250	snp	A/T	0.0119091	0.0762411	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971766	GCCGATTTACTGTTA[A/T]GTTTTAATGGCAACA	154214
rs62431251	snp	A/G	0.5	0	intron-variant	RNF217	GRCh38.p7	6:124998585	TGGGCGGATCATGAG[A/G]TCAGGAGATCAAGAC	154214
rs62433313	snp	A/G	0.00318978	0.0398085	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125006570	CAATGAAAGCATACT[A/G]TTCTGAGCAAATATA	154214
rs62433314	snp	C/T	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125020563	ATCTGGTTGTTGTTG[C/T]CTTTTTTTTTTTAAA	154214
rs62433315	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125033653	AGTGCCGCAATAAAC[A/T]TATGTGTGCATGTGT	154214
rs62433316	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125033661	AATAAACATATGTGT[A/G]CATGTGTCTTTATAG	154214
rs62433317	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125033691	GCAGCATGATTTATA[A/G]TCCTTTGGGTATATA	154214
rs62433318	snp	A/C	0.49614	0.0437598	intron-variant	RNF217	GRCh38.p7	6:125039053	ATCCCTGCTGTGTCC[A/C]TGTGTTCTTGTTGTT	154214
rs62433879	snp	A/G/T	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125054707	AATTGTGGCCTGGGC[A/G/T]ATGCAGTCACATGGT	154214
rs62433881	snp	G/T	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125068906	TGGAATGAAAGGAAG[G/T]ATTTAGTAGGATGAC	154214
rs62433882	snp	A/G	0.445592	0.155704	intron-variant	RNF217	GRCh38.p7	6:125071530	TGTGTGTGTGTGTGT[A/G]TGTGTGTATATCTTA	154214
rs62433883	snp	A/G	0.462909	0.131034	intron-variant	RNF217	GRCh38.p7	6:125071532	TGTGTGTGTGTGTGT[A/G]TGTGTATATCTTATT	154214
rs62433884	snp	A/G	0.482831	0.0910472	intron-variant	RNF217	GRCh38.p7	6:125071534	TGTGTGTGTGTGTGT[A/G]TGTATATCTTATTAC	154214
rs62433885	snp	C/T	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125072536	GCTAGAAAGTGCAAA[C/T]TTATTTAAATGAAAT	154214
rs62433887	snp	A/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088012	AAATAAGTTACAAAA[A/T]TCTTTTTTTTTTTTT	154214
rs62768263	snp	G/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088036	TTTTTTTTTTTTTTT[G/T]GAGACAGAGGTTCTC	154214
rs66477833	snp	C/T	0.0501905	0.150254	intron-variant	RNF217	GRCh38.p7	6:124988150	GGGATCTGGGTTGCA[C/T]GCTCCTTATGAGAAT	154214
rs66917505	in-del	-/A	0	0	intron-variant	RNF217	GRCh38.p7	6:125009986	AAAAAAAAAAAAAAA[-/A]GAATGCTAAGCTGTC	154214
rs66980280	snp	A/G	0.34303	0.232046	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088038	TTTTTTTTTTTTTTG[A/G]GACAGAGGTTCTCTC	154214
rs67041668	snp	C/G	0.0452528	0.143452	intron-variant	RNF217	GRCh38.p7	6:125080174	ATGTGCTTATATATT[C/G]TAAACTCTTAAGCAT	154214
rs67446157	multinucleotide-polymorphism	GC/TT	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125031885	GTCCATTTTCACACT[GC/TT]TGACAAAGACATACA	154214
rs67458734	snp	A/T	0.400325	0.199756	intron-variant	RNF217	GRCh38.p7	6:125016841	AATATAGATGATGGG[A/T]TGATGGGTGCAGCAA	154214
rs67895703	in-del	-/CA	0.202651	0.245475	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091646	AGTTGAAATGACTCT[-/CA]GTTTTATCTATAGCT	154214
rs68067092	in-del	-/A	0.375996	0.215928	intron-variant	RNF217	GRCh38.p7	6:124984548	TCTTTTTTTTTTTTT[-/A]TTTTTTTGAGAAAGG	154214
rs71024708	in-del	-/AGTGTAAGGA	0	0	intron-variant	RNF217	GRCh38.p7	6:124976304	TCCAGCCCAGGTGAC[-/AGTGTAAGGA]AGGGAGGAAGGGAGG	154214
rs71541260	multinucleotide-polymorphism	GA/TT	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125038242	AGTTGTATTAGCATT[GA/TT]ACACACGGAGCAGCA	154214
rs71551735	in-del	CACTC/TACT	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125066998	TGAACCCTCGTATAA[CACTC/TACT]CCTGCAACATTCCAC	154214
rs71561832	snp	G/T	0.154661	0.231107	intron-variant	RNF217	GRCh38.p7	6:125024635	AGGCACGAGAGAATC[G/T]CTTGAGCCCGGGAGG	154214
rs71706851	in-del	-/AC			intron-variant	RNF217	GRCh38.p7	6:125060357	AGTATATATGTGTAT[-/AC]ACACACACACACACA	154214
rs71755084	in-del	-/ATAG			intron-variant	RNF217	GRCh38.p7	6:125074349	TAGATAGATAGATAG[-/ATAG]GGATGGGAGGAAGGG	154214
rs72268010	in-del	-/TACT	0.0532157	0.154195	intron-variant	RNF217	GRCh38.p7	6:125062417	TCCTCATGATCAAGA[-/TACT]TACTTACAAGTATGA	154214
rs72551973	in-del	-/AA/CA			intron-variant	RNF217	GRCh38.p7	6:124997460	CAGGTTCACACAACT[-/AA/CA]CRAGTTAATATATTC	154214
rs72613291	snp	A/G	0.0256215	0.110247	intron-variant	RNF217	GRCh38.p7	6:124976695	CTTTTTCTAGAGATG[A/G]GGTTTCACCATGTTG	154214
rs72613292	snp	A/G	0.172028	0.23753	intron-variant	RNF217	GRCh38.p7	6:124987241	TATGTTTCACATATC[A/G]TATAGTTCACATATT	154214
rs72613293	snp	A/C	0.0263992	0.111815	intron-variant	RNF217	GRCh38.p7	6:124997966	CATGTTGAATCCTGA[A/C]TGTCTGCCTGACTCC	154214
rs72613294	snp	A/G	0.0905309	0.192535	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125006639	TTATTTCTGAGTTTT[A/G]ATTTTTACTATTAAA	154214
rs72963780	snp	A/C	0.463451	0.130149	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961695	ACAGCATTTAGAATT[A/C]ATAATCCTTAGCATT	154214
rs72967607	snp	C/T	0.405082	0.196086	intron-variant	RNF217	GRCh38.p7	6:124972012	CAAGTGTCATATAGC[C/T]ATCTCTCTCCTGAAC	154214
rs72969649	snp	C/T	0.145642	0.227177	intron-variant	RNF217	GRCh38.p7	6:125025817	TTTACAAATGTACTC[C/T]CTTATGAGTGGGGAA	154214
rs72969682	snp	A/G	0.0456336	0.143994	intron-variant	RNF217	GRCh38.p7	6:125046237	GAGAGGCAGCTGATC[A/G]GGCAGATAAGAGCAG	154214
rs72969686	snp	C/T	0.033436	0.1249	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125048216	ATGGCCACAGTATGG[C/T]ACCCTGTACTGAGAC	154214
rs72969688	snp	A/G	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:125048683	TGAAGTTTGAGACCT[A/G]AAATATCATATATGG	154214
rs72971305	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125062243	TTATGTATTAAGCAT[C/T]ACTTCTCTCTTAGTG	154214
rs72971326	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125076156	AAAAAGGTATTGCAA[A/G]TACATTTATATCTGC	154214
rs73578097	snp	A/G	0.0908922	0.192833	intron-variant	RNF217	GRCh38.p7	6:125033128	TTTCAATATATCCAA[A/G]GCCATATAATTAATA	154214
rs73579224	snp	A/G	0.0103295	0.0711199	intron-variant	RNF217	GRCh38.p7	6:125021581	GAAAATGCTTACCTT[A/G]TGTTACATGGAAAAG	154214
rs73579225	snp	A/G	0.0475351	0.146656	intron-variant	RNF217	GRCh38.p7	6:125022717	AATAGTCCAGAACAG[A/G]ATGCTGATTTTTCTA	154214
rs73580021	snp	A/G	0.209997	0.246779	intron-variant	RNF217	GRCh38.p7	6:125054124	GTGAACTTGTGGGCT[A/G]TTGGAGAGATTAGAC	154214
rs73580024	snp	A/C	0.20511	0.245937	intron-variant	RNF217	GRCh38.p7	6:125060596	ATTACAGGCATGAGC[A/C]ACCATGCCTGAGTAA	154214
rs73580031	snp	A/G	0.0134861	0.0810011	intron-variant	RNF217	GRCh38.p7	6:125067560	AAATATTTAGTATGG[A/G]TATCTAAATGGATGG	154214
rs73580047	snp	A/G	0.00883572	0.0658771	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125076745	GTGGTGAGAGATACC[A/G]CCAGCTCCGATTTTT	154214
rs73770781	snp	A/G	0.0248432	0.108648	intron-variant, upstream-variant-2KB, missense	RNF217, RNF217-AS1	GRCh38.p7	6:124963829	GGAGAAAAGAATTGG[A/G]ATAAATATTTCAGAC	154214
rs73770783	snp	C/T	0.00835141	0.0640778	intron-variant	RNF217	GRCh38.p7	6:124970339	AGTGATACAGGCGAA[C/T]GCAGTTTGAACTGGT	154214
rs73770785	snp	C/T	0.0505692	0.150756	intron-variant	RNF217	GRCh38.p7	6:124989269	GTATAACTACAGTCT[C/T]ACTGCATAATAAACA	154214
rs73770786	snp	C/G	0.0166325	0.0896639	intron-variant	RNF217	GRCh38.p7	6:124992144	GTAATGCCAGTAATG[C/G]TGACCTGCAGCATCA	154214
rs73770787	snp	A/G	0.0391387	0.134304	intron-variant	RNF217	GRCh38.p7	6:125003043	GTAATAATAGTGGTA[A/G]CCAAAGATTAAATGG	154214
rs73770789	snp	A/G	0.152667	0.230274	intron-variant	RNF217	GRCh38.p7	6:125004708	GTTAAAATTATAAAT[A/G]CCTAAATATATGCAC	154214
rs73770791	snp	C/T	0.156319	0.231784	intron-variant	RNF217	GRCh38.p7	6:125007704	TGTCTTATAGTCATC[C/T]TTACTGGGGGGAAAC	154214
rs73770792	snp	A/G	0.156319	0.231784	intron-variant	RNF217	GRCh38.p7	6:125007797	ATGTAGGGGGCATAC[A/G]TTCCAAGACTCCCAG	154214
rs73770795	snp	A/G	0.183886	0.241099	intron-variant	RNF217	GRCh38.p7	6:125013351	TTGCATGTTTTGTGT[A/G]TGTGTGTGTGTGTGT	154214
rs73772615	snp	A/G	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125052288	TGTCATGCGTTTTGT[A/G]TGTGTGTGTGTGTGT	154214
rs73772618	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125071240	AAGTAACATGCGTTT[A/G]GTAGAAACCATATTT	154214
rs73772620	snp	A/G	0.0349115	0.127424	intron-variant	RNF217	GRCh38.p7	6:125073453	ATTATTTTGCTTAAA[A/G]AAGGATTCTCAAATT	154214
rs73772624	snp	A/C	0.0341408	0.126114	intron-variant	RNF217	GRCh38.p7	6:125076144	GAGCTGAAAACTAAA[A/C]AGGTATTGCAAATAC	154214
rs73772626	snp	C/T	0.0345262	0.126772	intron-variant	RNF217	GRCh38.p7	6:125078384	CACCTTTAATTTGGT[C/T]GTGGCAGTGTGTTTC	154214
rs74331705	snp	A/G	0.0244538	0.107838	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090764	TATTTTTCAAGTTTA[A/G]AATGGACCGGGTTGA	154214
rs74344593	snp	A/G	0.0209421	0.100162	intron-variant	RNF217	GRCh38.p7	6:125005212	CCATAACAGGCCTGT[A/G]TGTTAGGTTTATAAC	154214
rs74350699	snp	C/T	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125020565	CTGGTTGTTGTTGCC[C/T]TTTTTTTTTTAAATT	154214
rs74406940	snp	C/T	0.00874735	0.0655527	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088504	AGACTATTCTCATTG[C/T]TTCTTTGGAGCATTA	154214
rs74408364	snp	C/T	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125014627	AATTATGGTCAGAAG[C/T]AGTTCAAAATCACAC	154214
rs74516762	snp	A/C	0.0205511	0.0992634	intron-variant	RNF217	GRCh38.p7	6:124993009	TAGACTGAGAAACAA[A/C]TGTCAGTGCTCTTGC	154214
rs74527417	snp	A/G	0.0611083	0.163768	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085101	ACATATATACCAACG[A/G]GCTGAATAACATACT	154214
rs74689753	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125078999	CCACTGTCCTTGTGT[G/T]ATGTGACACAACTTG	154214
rs74714636	snp	A/G	0.0103295	0.0711199	intron-variant	RNF217	GRCh38.p7	6:124980751	TGTTGATTTTATGCT[A/G]AATGACTGAGTTGCC	154214
rs74763691	snp	C/T	0.00517822	0.0506191	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088358	GGGACTCCTTTGAAA[C/T]TCTGATTTTGAAAAT	154214
rs74775028	snp	A/G	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:124978367	CCTGTGCCCACCGTG[A/G]CTCTGCGCTCAGCCC	154214
rs74829915	snp	A/G	0.0130921	0.0798413	intron-variant	RNF217	GRCh38.p7	6:125055733	CTTAATGTTAGATGC[A/G]TAAGGAAAAGCAATT	154214
rs74885812	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125043399	TTCTGATCCCCCCAG[A/G]TCTGAGATTACTATA	154214
rs74895810	snp	A/G	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:125071394	TTGCCAGCATTTTTT[A/G]GATATTGTGTTTTGT	154214
rs74937746	snp	C/T	0.0898077	0.191933	intron-variant	RNF217	GRCh38.p7	6:124997671	GGAAACAGCCTGTGG[C/T]GATGAGATACCTGGA	154214
rs74940037	snp	A/C	0.0513262	0.151752	intron-variant	RNF217	GRCh38.p7	6:125082793	TGCAAATAAATAAAC[A/C]TAGACATTTTAAAAT	154214
rs74941739	snp	A/G	0.0333695	0.124785	intron-variant	RNF217	GRCh38.p7	6:125032340	TCAATTTTGATAGGT[A/G]GAACTCCATACCCAT	154214
rs74947689	snp	A/T	0.00636936	0.0560724	intron-variant	RNF217	GRCh38.p7	6:125082203	GCAGCTGGTTCAGGG[A/T]CCATACTTTGAGAAC	154214
rs75008772	snp	C/T	0.153	0.230415	intron-variant	RNF217	GRCh38.p7	6:125062610	AGATGGAGTCTCACT[C/T]TTTTCACCCGGGATG	154214
rs75121814	snp	A/G	0.0298908	0.118541	intron-variant	RNF217	GRCh38.p7	6:124973234	CTCTGCATCCTCTTC[A/G]GTCCCTTCTTCTATC	154214
rs75170616	snp	A/G	0.164546	0.234942	intron-variant	RNF217	GRCh38.p7	6:125078061	TGAGGTTAATGGAAC[A/G]TAATTTTCCACAGCC	154214
rs75211966	snp	A/G	0.0341408	0.126114	intron-variant	RNF217	GRCh38.p7	6:124973129	TAAATGAAAATTTCA[A/G]TATTTCATTTTCTTG	154214
rs75279605	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124984557	AAAAAAAAAAAAAAA[A/G]AAAAGAAAGAAAGAA	154214
rs75291018	snp	G/T	0.0228947	0.104514	intron-variant	RNF217	GRCh38.p7	6:125056579	AGAAGAGCTGTGATT[G/T]TAATTGCCACTCAGC	154214
rs75379897	snp	C/T	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:124978651	CAGCTCCTTTATTCT[C/T]GTCGCCCACAGCTCA	154214
rs75469355	snp	C/T	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:125067561	AATATTTAGTATGGG[C/T]ATCTAAATGGATGGT	154214
rs75547663	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124977079	TCTACAAACTAAAAA[C/T]TTGGAATCAGAATTT	154214
rs75591276	snp	C/T	0.0115144	0.0749975	intron-variant	RNF217	GRCh38.p7	6:125010517	CTATACCAATTTCCA[C/T]TTCTTCTGATGCAAA	154214
rs75632851	snp	C/T	0.0182019	0.0936463	intron-variant	RNF217	GRCh38.p7	6:124972588	AACTGTCCCACTACA[C/T]CTATAGAGATATTAA	154214
rs75719670	snp	C/G	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125046161	TGAGTAAGTGCACGG[C/G]CCCCGAGGCTAAGGC	154214
rs75738321	snp	C/T			stop-lost, utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125082935	ACAGGTATGCACTGG[C/T]AACATGCAGATGATT	154214
rs75761367	snp	A/G	0.0547245	0.156101	intron-variant	RNF217	GRCh38.p7	6:125043712	ATTTGAATTATAATA[A/G]CATCGTAACACTGTA	154214
rs75797338	snp	A/G	0.0425829	0.139564	intron-variant	RNF217	GRCh38.p7	6:125014977	ATGCACTGGTCCTGT[A/G]TTGTGTAAATATATT	154214
rs75801973	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124969688	TTTAGGCTCTGGGGA[C/T]ACAAGAGACTAAAAC	154214
rs75804258	snp	C/T	0.0170251	0.090679	intron-variant	RNF217	GRCh38.p7	6:124979177	AGGACCTGACCCTGT[C/T]TGCCTACAAATTTGT	154214
rs75811105	in-del	-/AA			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961511	AGGGTTAAAAAAAAA[-/AA]CTTCTAAGAGAACAC	154214
rs75849566	snp	A/G			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009483	AGGCAGAAAAAAAAA[A/G]GAAAAACAGAGACTA	154214
rs75872615	snp	C/T	0.0150606	0.0854603	intron-variant	RNF217	GRCh38.p7	6:125004525	GCAAATTAAAGATAA[C/T]GAGAATGACTTTCTT	154214
rs75889541	snp	G/T	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125032722	TATGAACTATGATCA[G/T]TTTTGAGCTTATTTT	154214
rs75991824	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125021216	TCTACTCTCTGAAGT[A/G]TTATACAATGTTCAG	154214
rs76177793	snp	A/T	0.0287284	0.116357	intron-variant	RNF217	GRCh38.p7	6:125062559	ATTTGAATCTTATTG[A/T]TCCTTTTGTTTGTTT	154214
rs76178110	snp	A/G	0.0558544	0.157504	intron-variant	RNF217	GRCh38.p7	6:125070541	ATTATGGCCATTCTT[A/G]TAGGAGTAAGGTGGT	154214
rs76194917	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125015097	CACTTAGCAATCACT[C/T]AGAAGTTTCATTGAT	154214
rs76344567	snp	A/G	0.00279162	0.0372561	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089649	AGTACATAACAGGAA[A/G]GAAAAAGGGAGAGAC	154214
rs76344600	snp	A/C/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125019837	CTTTTTTGCAGTGGG[A/C/G]GGGGAGTGAAAAAAT	154214
rs76384386	snp	A/G	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125072115	GGGGAATTCATCAGC[A/G]TAAGAAATGTATTAT	154214
rs76551797	in-del	-/GAA			intron-variant	RNF217	GRCh38.p7	6:124984560	AAAAAAAAAAAAAAA[-/GAA]AGAAAGAAAGAAAAT	154214
rs76617896	snp	A/G	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:125053922	GTTCATTAGGACAAT[A/G]TATTTAGTAAACATC	154214
rs76653698	snp	A/G	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125037090	TTGAAAAAAAAAAAA[A/G]GTCCTGCCCACTGCC	154214
rs76674333	snp	A/T	0.00478085	0.0486577	intron-variant	RNF217	GRCh38.p7	6:125067048	CACCATCTTGAGGAA[A/T]CCAAGGGAGCTAGGT	154214
rs76710364	snp	C/T	0.0329836	0.124112	intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967362	GTACTATGTTCATTT[C/T]AGAAATCTTCCACCA	154214
rs76740197	snp	A/G	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:125072728	TGGCAAAAACAAGAA[A/G]ACACAGATATACCTT	154214
rs76789863	snp	A/G	0.0166325	0.0896639	intron-variant	RNF217	GRCh38.p7	6:124999131	GGAAAAACATACTGT[A/G]TATTATACTGAAGAC	154214
rs76849906	snp	A/G	0.0170251	0.090679	intron-variant	RNF217	GRCh38.p7	6:124975107	AGCTAATTATAGGCT[A/G]CCTGGCAAATTGCTT	154214
rs76862620	snp	C/T	0.030665	0.119967	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009461	TCTTTCTAGAAAGAA[C/T]GTAAGAAGGCAGAAA	154214
rs76875071	snp	A/T	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125037092	GAAAAAAAAAAAAAG[A/T]CCTGCCCACTGCCCT	154214
rs77026276	snp	A/G	0.0850919	0.187897	intron-variant	RNF217	GRCh38.p7	6:125047502	ATAACATTTCCCAGA[A/G]GTCAGGCTTCTCCAA	154214
rs77028369	snp	A/G	0.0295035	0.117819	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085938	CTCATTCTTTTATAA[A/G]TTACTGCATAATCCA	154214
rs77182504	snp	C/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:125059567	TCCAAGTTAGCCTGG[C/T]TCTACAACTGGATTT	154214
rs77222230	snp	A/C	0.00636936	0.0560724	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086521	GCCATTGTGAAAAGT[A/C]GGAAAGAATATGTTG	154214
rs77249425	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124987042	TTTGCCGAATATAGA[C/T]ATTAGTCTACTAGCA	154214
rs77274874	snp	A/G	0.0275645	0.114116	intron-variant	RNF217	GRCh38.p7	6:124997418	CAATTACTTAACCAT[A/G]TGCGAAAGTGACTGT	154214
rs77351256	snp	A/G	0.0130921	0.0798413	intron-variant	RNF217	GRCh38.p7	6:125016513	TTTAATGGAATCTGT[A/G]CAGAAAAGTATTAAC	154214
rs77459765	snp	C/T	0.00318978	0.0398085	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090630	GAAAATTAGAAGAAA[C/T]TTCTTGATCATAAGA	154214
rs77496024	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125050013	TGAAGGGGATTGTCA[C/T]TGAACTTACGAAAAT	154214
rs77556648	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:124979351	AGAAAGGAGTTAGGC[A/G]TGGGCAGCTCTCTAA	154214
rs77602413	snp	A/C	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125071739	CTAAATATTCAATTC[A/C]TTAAATGTCAGTCAT	154214
rs77616351	snp	A/C	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125067659	AGCCATGAAATGATG[A/C]TGAGTTTGGTTTTGT	154214
rs77632291	snp	C/G	0.0111196	0.0737302	intron-variant	RNF217	GRCh38.p7	6:125066016	TCCAGCTGCTCAGGC[C/G]AAGAACTTTAGGTTA	154214
rs77643155	snp	A/C	0.0123036	0.0774623	intron-variant	RNF217	GRCh38.p7	6:125043492	TGCAAAGCTTCAGTA[A/C]CTAGCCCGTACCTGC	154214
rs77687766	snp	A/G	0.0916144	0.193427	intron-variant	RNF217	GRCh38.p7	6:125068963	AAGATGAAGCTGAAG[A/G]AGGGGAAAACTGGCA	154214
rs77696651	snp	G/T	0.0275645	0.114116	intron-variant	RNF217	GRCh38.p7	6:124994922	TGAGGTATACTACGA[G/T]AATTTTTTATGATCC	154214
rs77760169	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125025090	AAAATCAGGAATGTG[A/C]TGTGCTAGAGGTCAA	154214
rs77783960	snp	A/C	0.0174175	0.0916809	intron-variant	RNF217	GRCh38.p7	6:125064739	ATTTTAAAATGAGGA[A/C]AAAATAAGTACGTGT	154214
rs77847763	snp	A/C	0.00478085	0.0486577	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087144	CAAATGAGGGCACAT[A/C]TGCCAAGACATCAGT	154214
rs77865050	snp	A/G	0.00914312	0.0669923	intron-variant	RNF217	GRCh38.p7	6:124972410	TTACTCTCCACACAT[A/G]TGCCAGAGGGTTCTT	154214
rs77876150	snp	C/T	0.00795532	0.062565	intron-variant	RNF217	GRCh38.p7	6:124999094	TTCTTAAGGTGACTT[C/T]GTGCCTCTAAAAAGC	154214
rs77905247	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125011578	ACTTGGAAAAAAATC[A/G]CTCGGTTAATGTCTG	154214
rs77906933	snp	A/G	0.0263992	0.111815	intron-variant	RNF217	GRCh38.p7	6:125005478	CAGGCAAGAGAATAA[A/G]CTTGATCTCTGCAGG	154214
rs78038884	snp	A/G	0.0611083	0.163768	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084325	TTTTCTCAACCTACA[A/G]AAGCTTTAAAAATAA	154214
rs78078717	snp	A/G	0.0368353	0.130617	intron-variant	RNF217	GRCh38.p7	6:125015984	AGAAAGCACAATACA[A/G]AGCAGTATGTGTCTA	154214
rs78109568	snp	A/G	0	0	intron-variant	RNF217	GRCh38.p7	6:124997462	AGGTTCACACAACTC[A/G]AGTTAATATATTCCC	154214
rs78134897	snp	C/T	0.151334	0.229706	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089609	GATTTAGATATGCCA[C/T]ACTCAATATATTTAG	154214
rs78278280	snp	A/G	0.00914312	0.0669923	intron-variant	RNF217	GRCh38.p7	6:125062796	TGACCAGCTTATCTC[A/G]AACTCCTGATCTCAG	154214
rs78479972	snp	A/G	0.00438332	0.0466095	intron-variant	RNF217	GRCh38.p7	6:124978618	TTTTCCCATAGTCTG[A/G]CAAGCGGGAGTGTGC	154214
rs78497861	snp	C/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125016785	CCTTGCCCCCTACCC[C/G]CTGACAGGCCCCAGT	154214
rs78594179	snp	C/T	0.0329836	0.124112	intron-variant	RNF217	GRCh38.p7	6:125055486	AATGTGATAGTTCAG[C/T]ACTTAATCACAAAGA	154214
rs78618500	snp	C/T	0	0	intron-variant	RNF217	GRCh38.p7	6:125021269	TAACATGGAAAAAGC[C/T]TTTTTTTTTTTTTTT	154214
rs78709984	snp	A/G	0.00478085	0.0486577	intron-variant	RNF217	GRCh38.p7	6:125077971	AGAACATGTATACGC[A/G]AATGCACTTTCACAT	154214
rs78772892	snp	A/T	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125079314	CATATTACTTCTTAC[A/T]AAAATTCTAAGTTTT	154214
rs78783433	snp	A/G	0.02016	0.0983543	intron-variant	RNF217	GRCh38.p7	6:124974091	ATCCCAAGGGATGTG[A/G]AAGCTGCATGACATT	154214
rs78799143	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125016381	AAAAGGTGGGATATA[C/T]TAAAGCTGTGTTTTG	154214
rs78903668	snp	A/G	0.128632	0.218563	intron-variant	RNF217	GRCh38.p7	6:125049839	GGGGTAAAATTGACT[A/G]TGTCTGGAAGAGGAG	154214
rs78968193	snp	C/G	0.0225045	0.103662	intron-variant	RNF217	GRCh38.p7	6:124978882	AGCAAAGCTGTCAGC[C/G]GACAGGGCACCCTGA	154214
rs79048000	snp	C/T	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125005599	TCCTTTGAAAATCTT[C/T]TGAAAGAACTTTTTT	154214
rs79052351	snp	C/T	0	0	intron-variant	RNF217	GRCh38.p7	6:125009987	ACAGCTTAGCATTCT[C/T]TTTTTTTTTTTTTTA	154214
rs79156970	snp	A/G	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:124996514	TTCTATTTTTATGAT[A/G]TCTTTTATGAAGAGT	154214
rs79231474	snp	C/G	0.0501905	0.150254	intron-variant	RNF217	GRCh38.p7	6:124998404	GCCTCATGTAAATCT[C/G]TCTGCTTATCTCCAT	154214
rs79280246	snp	C/T	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125033198	ACAGATTCTGTGTTC[C/T]TTTTTTTTTTTTATA	154214
rs79315560	snp	C/T	0.0364509	0.129988	intron-variant	RNF217	GRCh38.p7	6:125013942	AGAAACATAATGCCC[C/T]GCTGACTACATGTGC	154214
rs79390940	snp	G/T	0	0	intron-variant	RNF217	GRCh38.p7	6:125013346	GGTGCTTGCATGTTT[G/T]GTGTATGTGTGTGTG	154214
rs79392876	snp	A/G	0.00874735	0.0655527	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125083165	AAAATGGTCACTTTC[A/G]TAAACTATAAACATC	154214
rs79414219	snp	A/G	0.0322114	0.122752	intron-variant	RNF217	GRCh38.p7	6:125050157	TAGGTGCAATTCTGG[A/G]TTTCATTCTTATTCC	154214
rs79418529	snp	C/T	0.0174175	0.0916809	intron-variant	RNF217	GRCh38.p7	6:125064350	TAGTTGTTAGAAGCA[C/T]GATTGTTTGACGGCA	154214
rs79421499	snp	C/T	0.0535932	0.154675	intron-variant	RNF217	GRCh38.p7	6:125066034	GAACTTTAGGTTATC[C/T]CAGACTCTGCTTCTT	154214
rs79489741	snp	C/G	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125082661	ATTATTATTAAACTG[C/G]TATCACTGAGGGTGC	154214
rs79533736	snp	C/T	0.0490535	0.14873	intron-variant	RNF217	GRCh38.p7	6:125059623	ACGTTGGGGAAATTC[C/T]GAATAAACTGATGTA	154214
rs79596915	snp	A/G	0.0916144	0.193427	intron-variant	RNF217	GRCh38.p7	6:125067953	AGCAATAGTGTATCA[A/G]AGGTCAGTAAGGAGG	154214
rs79710943	snp	C/T	0.0166325	0.0896639	intron-variant, upstream-variant-2KB, synonymous-codon	RNF217, RNF217-AS1	GRCh38.p7	6:124964314	AGGTGCCAACTCTTC[C/T]GTGAAGCGTTGCCTC	154214
rs79779196	snp	A/C	0.0209421	0.100162	intron-variant	RNF217	GRCh38.p7	6:125054869	ATGTTTCTGGCCCTG[A/C]AACCACACTTTGAGC	154214
rs79876099	snp	A/G	0.0737376	0.17729	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981462	CCAAACATTGGTTTG[A/G]TTGGGGGGGCGGTGA	154214
rs79899494	snp	C/T	0.0718919	0.175435	intron-variant	RNF217	GRCh38.p7	6:125050317	ATAATCCCCATTCTT[C/T]TTCCCACAAATGTTA	154214
rs79903450	snp	C/T	0.0433465	0.140692	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125006406	TTCCTAGCATAGTTA[C/T]TATTATAATATTATT	154214
rs79942604	snp	A/G	0.030278	0.119257	intron-variant	RNF217	GRCh38.p7	6:125073012	CATAATAGGCTCTAC[A/G]CAAAAATTAGCGCTC	154214
rs79977753	snp	C/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125041583	GAGGCAAATCAGACA[C/T]CTTCTGACTGGAGCC	154214
rs80006374	snp	A/G	0.0162398	0.0886349	intron-variant	RNF217	GRCh38.p7	6:125063443	TCTGGATTCTGATAC[A/G]CCATCTCTATACAAA	154214
rs80036297	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125026045	GATAGCCCATATGAT[C/G/T]GTGGAGACCATCTGC	154214
rs80039879	snp	C/T	0.0217236	0.101931	intron-variant	RNF217	GRCh38.p7	6:125077173	CAGTGTCATGTATAT[C/T]TTTGTAATGGACAAT	154214
rs80073034	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125066277	AACGCAGATTACATC[A/T]CTCTGCTCAAAATTG	154214
rs80080541	snp	A/G	0.0539704	0.155153	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091564	ATATTAAACACCAGA[A/G]ATTAAAGCCATTAAA	154214
rs80158870	snp	A/G	0.155987	0.23165	intron-variant	RNF217	GRCh38.p7	6:125008041	GCGGGTGGATCACGA[A/G]GTCAGTAGATCAAGA	154214
rs80165157	snp	A/C	0.00795532	0.062565	intron-variant	RNF217	GRCh38.p7	6:125071689	ATTTCATCTTATGAC[A/C]TTAAGTATAGAAAGA	154214
rs80194656	snp	C/G	0.0189856	0.0955633	intron-variant	RNF217	GRCh38.p7	6:124978512	GGGGGTTACAGTTCT[C/G]GCTTGTGGAGTCCCA	154214
rs80201123	snp	C/G	0.096524	0.197345	intron-variant	RNF217	GRCh38.p7	6:125075144	AAAACATTATGAGAT[C/G]GTTTTTGCAATTTTT	154214
rs111231912	snp	A/G	0.108048	0.20579	intron-variant	RNF217	GRCh38.p7	6:125035755	ATGTTCTTTTTGATT[A/G]TCTTTAGAAGCTTTT	154214
rs111232017	snp	A/T	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:125042454	CATCTGATTGCCTCT[A/T]TGTGTTCAATAAAAT	154214
rs111232976	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125021289	TTTTTTTTTTTGAGA[C/T]GGAGTCTTGGTCTGT	154214
rs111351058	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125034857	TTCCATTTGTTTGTA[C/T]CCTCTTTTATTTCAT	154214
rs111356425	in-del	-/A	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125008255	ATAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAGT	154214
rs111406001	snp	A/G	0.5	0	intron-variant	RNF217	GRCh38.p7	6:124993676	TTAGAGCTAGGTGCA[A/G]GTGCTGGGCGGCACA	154214
rs111414331	snp	A/G	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125054513	CTCTTCTCTGTCTTT[A/G]CCTCCATGAAGGCAT	154214
rs111421344	snp	A/G	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125056279	CAAGTTATTTAATCT[A/G]TCTGAGTCTCATTTC	154214
rs111436790	in-del	-/CTTCCTTACA	0.5	0	intron-variant	RNF217	GRCh38.p7	6:124976302	TTCCTCCCTTCCTCC[-/CTTCCTTACA]CTGTCACCTGGGCTG	154214
rs111443807	in-del	-/T	0	0	intron-variant	RNF217	GRCh38.p7	6:125040695	TTTGGTTTGCCAGTA[-/T]TTTATTGAGGATTTT	154214
rs111446640	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124984558	AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA	154214
rs111460767	in-del	-/T	0	0	intron-variant	RNF217	GRCh38.p7	6:125026656	TCTGAGAAAAAAAAA[-/T]AGGGAATCACAGTTA	154214
rs111503177	snp	A/C	0.0244538	0.107838	intron-variant	RNF217	GRCh38.p7	6:125036925	TATTTATTATAAAGC[A/C]GGAAATAACAGATGG	154214
rs111520357	snp	A/G	0.0252325	0.109451	intron-variant	RNF217	GRCh38.p7	6:125053473	TATATTTGCAGTGCT[A/G]CTTTACACATGGATG	154214
rs111560210	snp	A/G	0.5	0	intron-variant	RNF217	GRCh38.p7	6:124970913	GTTCCAGCAGGATGA[A/G]GTTTGAAATTGACCA	154214
rs111613817	snp	A/C	0.00438332	0.0466095	downstream-variant-500B	RNF217	GRCh38.p7	6:125093040	CAATGATTTTCCTAG[A/C]TCTGTCACTAAGGAA	154214
rs111656876	snp	C/T	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125031033	CTTTGCACATGCACG[C/T]GGAACACCACATGGA	154214
rs111658916	snp	A/G	0.127599	0.217986	intron-variant	RNF217	GRCh38.p7	6:125039562	AAAATTAACAAGGAC[A/G]TTGAGGACTTGAACT	154214
rs111669612	snp	C/G	0.00438332	0.0466095	intron-variant	RNF217	GRCh38.p7	6:124989572	TCACACAAAAGCAGC[C/G]ATAAACAGTGCATAA	154214
rs111695036	snp	C/T	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125071535	GTGTGTGTGTGTGTG[C/T]GTATATCTTATTACA	154214
rs111734761	snp	A/G	0.00716266	0.059414	intron-variant	RNF217	GRCh38.p7	6:125030957	TTTGCCTGGGCATCC[A/G]GGCGTTTCCCTACAT	154214
rs111778320	snp	C/T	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125055405	CACAAAGCGTCAGAT[C/T]CTTTATTATTCTGAT	154214
rs111814408	snp	A/T	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125031821	TTCCACATTTTCGGG[A/T]ATCTTTTCAGCAATG	154214
rs111818902	snp	C/G	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:125041395	CCAAGAAGAGCATGT[C/G]AGTCCTCCTCATAAA	154214
rs111835374	snp	A/G	0	0	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009771	TCCATCTCCGTGCAC[A/G]TTCGTTGGGAGAACT	154214
rs111898147	snp	C/G	0.0146672	0.084371	intron-variant	RNF217	GRCh38.p7	6:125039443	AGGAGCACCCAGATT[C/G]ATAAAACGAGTTCTT	154214
rs111906649	snp	G/T	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125053699	GGCAGGTGAGTCGGC[G/T]TACTTTCATCTCAGT	154214
rs111918156	snp	A/C	0.5	0	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961227	TCAGGAGAAAAAAAA[A/C]AAAACAAGGGCTGGC	154214
rs112011277	snp	A/C/G	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981586	TGAATCTGCCTTTTT[A/C/G]CATAAACAGCAAGGC	154214
rs112047604	snp	A/G	0.5	0	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086238	TTTTTAAAGAAAATC[A/G]TCTTTTGAAGGGTAA	154214
rs112059626	snp	A/G	0.5	0	intron-variant	RNF217	GRCh38.p7	6:124991404	TAGTGGCCTTCTTTT[A/G]GCAACCCATGTATAC	154214
rs112075959	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124989637	TTTGTAAACACTTAA[A/G]TTTGATATAATTTTC	154214
rs112116062	snp	A/G	0.00993419	0.0697739	intron-variant	RNF217	GRCh38.p7	6:125061521	ATATTTTTATTATCA[A/G]ATTTTATGAGCTCTT	154214
rs112150051	in-del	-/TATAA	0.0341408	0.126114	intron-variant	RNF217	GRCh38.p7	6:124973564	TGATTGAAAATAAAT[-/TATAA]TATGTTTGCTATAAA	154214
rs112151477	snp	A/G			intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967086	TTGATTTAGAGCTCT[A/G]AATCCAAGGCAGAGA	154214
rs112174512	snp	A/G	0.040671	0.13668	intron-variant	RNF217	GRCh38.p7	6:125026911	GAGTAATTGTGTTTT[A/G]GATACAGTAAATATT	154214
rs112185219	snp	A/G	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125016179	AACTTAATAACTGCT[A/G]GAGGCATATGGTTCT	154214
rs112194178	snp	C/T	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:125050320	ATCCCCATTCTTCTT[C/T]CCACAAATGTTAAGC	154214
rs112247982	in-del	-/A	0.0876345	0.190099	intron-variant	RNF217	GRCh38.p7	6:125066738	CAGCTGTGAGAGCAG[-/A]GATTTGATCTATTTT	154214
rs112279020	snp	C/T	0.0383715	0.133092	intron-variant	RNF217	GRCh38.p7	6:125066252	CAGCTAGAATGATGC[C/T]GTTAAACATAACGCA	154214
rs112375380	snp	A/G	0.0115144	0.0749975	intron-variant	RNF217	GRCh38.p7	6:125032978	CTTTCCAAATTACAC[A/G]TGAGTGTGGTTTTAT	154214
rs112459056	snp	C/T	0.0138799	0.0821421	intron-variant	RNF217	GRCh38.p7	6:125020484	TCTTTCTCAGAATGA[C/T]GGGCTGGAGCCTAGT	154214
rs112480218	snp	C/G	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125072854	AGCATAATAAAGAAA[C/G]ACATGGATTCAAAAT	154214
rs112538609	in-del	-/A	0.367913	0.220446	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009474	AATGTAAGAAGGCAG[-/A]AAAAAAAAAGAAAAA	154214
rs112576766	snp	A/T	0.00597247	0.0543191	intron-variant	RNF217	GRCh38.p7	6:125070500	CACCACATTCACACC[A/T]ACATCTATTGTTTTT	154214
rs112717779	snp	G/T	0.5	0	intron-variant	RNF217	GRCh38.p7	6:124990418	AATATATCTGCAATT[G/T]ATTTTATAAGAGATA	154214
rs112719336	snp	A/G	0.00438332	0.0466095	intron-variant	RNF217	GRCh38.p7	6:124972922	CTGCTCTGTGCTTCC[A/G]TTAGACTACAAAGCT	154214
rs112725996	snp	C/T	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125002798	TAAGTACTTACTGTG[C/T]ATTGTGGAATCTATT	154214
rs112741001	snp	A/G	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125077011	AAGAATAAAATTTAA[A/G]ACTTAAATTTTGTTA	154214
rs112743330	snp	G/T	0.0463947	0.145069	intron-variant	RNF217	GRCh38.p7	6:125052284	ACCTTGTCATGCGTT[G/T]TGTGTGTGTGTGTGT	154214
rs112809827	snp	A/G	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125029068	AGAACAGGATTCTCT[A/G]AAATGTATTTTCAAT	154214
rs112840591	snp	C/G	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125069313	TAGTCTACTGTGATA[C/G]AAGCAGCTGTTTCTT	154214
rs112894975	in-del	-/TTTGAG	0.0256215	0.110247	intron-variant	RNF217	GRCh38.p7	6:124989637	TTGTAAACACTTAAA[-/TTTGAG]TTTGATATAATTTTC	154214
rs112903308	snp	C/T	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:125032626	GTTTCTGGAAGGAAA[C/T]GACAACCATTTTGTG	154214
rs112906578	snp	C/T	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:124987339	ACTTTTTTTATTCCC[C/T]CTAAGAGAAATCCCA	154214
rs112927716	snp	A/G	0.0916144	0.193427	intron-variant	RNF217	GRCh38.p7	6:125067607	AATAAAATAATGGAG[A/G]CAGAGTTAGAGTTAT	154214
rs112943638	in-del	-/T	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125044058	TTACTATGAATTTAG[-/T]TTTTTTTTTTTAATT	154214
rs112949290	snp	C/T	0.0217236	0.101931	intron-variant	RNF217	GRCh38.p7	6:125069889	TAGTTTTTGGGGTAC[C/T]GTTGGTTTTTGGTTA	154214
rs112978294	snp	A/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124973809	ACAGATTCTTCCAGA[A/T]CCTAGGAACATAAAA	154214
rs113010343	snp	C/T	0.0123036	0.0774623	intron-variant	RNF217	GRCh38.p7	6:125035355	TAGATAGCTCTCTCT[C/T]GGCAGAAACTCTACA	154214
rs113010735	snp	A/G	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125066982	ACACTATTGCACTTC[A/G]GTGGAATGTTGCAGG	154214
rs113016102	snp	C/T	0.0197687	0.0974348	intron-variant	RNF217	GRCh38.p7	6:125070942	GAAACTGGAGACAAA[C/T]ACTTGTGGGCAGATG	154214
rs113064255	snp	A/T	0.0244538	0.107838	intron-variant	RNF217	GRCh38.p7	6:125030356	CCAAAGTCTTAACTC[A/T]TTTCAGCATTAACCC	154214
rs113095882	snp	A/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125030516	TTCCAAATGGGAGCT[A/G]TTGGCCAAAAGGCCA	154214
rs113111128	snp	A/G	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125002900	TTGTAATAGTTCTGG[A/G]TCTACAGCATAAGGC	154214
rs113149022	snp	G/T	0.5	0	intron-variant	RNF217	GRCh38.p7	6:124985769	AGGAAGAGAGAGGTA[G/T]CAAGGAATTATATTC	154214
rs113161323	snp	A/G	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981726	ACTGTTTAACATAGA[A/G]TAAAGATCTTGGCCG	154214
rs113167308	snp	C/T	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:125036838	TGCCACTTAGAATGG[C/T]GATTAAAAAGCCAGG	154214
rs113169776	snp	C/T	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125001532	TGACAATTGAAATAA[C/T]TAAGTAAACTTATTC	154214
rs113181621	snp	A/T	0.0252325	0.109451	intron-variant	RNF217	GRCh38.p7	6:125055748	ATAAGGAAAAGCAAT[A/T]TTTTTCCTTCTTTCC	154214
rs113189603	snp	A/G	0.0158469	0.0875917	intron-variant	RNF217	GRCh38.p7	6:125040967	TAAGAGCTGTTTATG[A/G]CAAACCCATAGCCAA	154214
rs113220408	snp	A/G	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125052715	CATTTTCTCCTCTCT[A/G]TAACATGCTGTACCT	154214
rs113243840	snp	C/T	0	0	intron-variant	RNF217	GRCh38.p7	6:125061342	GCATTTTAAGTATTT[C/T]TTAAATATTAATTTA	154214
rs113299404	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124989636	ATTTGTAAACACTTA[A/G]ATTTGATATAATTTT	154214
rs113330934	snp	G/T	0	0	intron-variant	RNF217	GRCh38.p7	6:125004064	AAATGAGGGGTTACA[G/T]TTTTTTTCTTTAAAA	154214
rs113359186	snp	C/T	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125030818	GAGGACAGTGGCCCT[C/T]TTCTTGCAGCTCCAC	154214
rs113390342	snp	C/T	0.5	0	intron-variant	RNF217	GRCh38.p7	6:124994995	AAAAATGGGATGTTA[C/T]GTATCCAAGTATTAA	154214
rs113455879	in-del	-/T	0.5	0	intron-variant	RNF217	GRCh38.p7	6:124995882	GCCGAGATCGTGTCA[-/T]TTGCACTCCAGCCTG	154214
rs113456737	snp	A/G	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125052294	GCGTTTTGTGTGTGT[A/G]TGTGTGTGTGTGTGT	154214
rs113542766	snp	A/G	0.00438332	0.0466095	intron-variant	RNF217	GRCh38.p7	6:125037541	TAGAAAAATTCAAAG[A/G]CATCTAGCACTAAGC	154214
rs113570629	snp	A/G	0.0364509	0.129988	intron-variant	RNF217	GRCh38.p7	6:124990332	TATTCTGTATCTGCC[A/G]CTGGCTTTCTAATTT	154214
rs113572672	snp	A/G	0.00716266	0.059414	intron-variant	RNF217	GRCh38.p7	6:125016303	CACTCGAATTTTACC[A/G]TGAAGGAGAGAAGAG	154214
rs113592444	snp	C/T	0.0333695	0.124785	intron-variant	RNF217	GRCh38.p7	6:125065057	GAGGCGGGCGGATCA[C/T]GAGGTCAGGAGATCG	154214
rs113622961	snp	A/C	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125053862	TTGAAGCCCTGCTTG[A/C]CTCTTTTAGAAGAGT	154214
rs113733059	in-del	-/A	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125045143	AGTAATACTGTATAC[-/A]AAAAAAAAAAATGAA	154214
rs113782889	snp	C/T	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:125030960	GCCTGGGCATCCGGG[C/T]GTTTCCCTACATCTT	154214
rs113787744	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125045087	ACATTCATTATGTTA[C/T]CTTAAAAATTACACA	154214
rs113864225	snp	A/G	0.144296	0.226554	intron-variant	RNF217	GRCh38.p7	6:125030070	GCAGCAGCAAGAGAA[A/G]ATGAAGAAGAAGCAA	154214
rs113962504	snp	G/T	0.0252325	0.109451	intron-variant	RNF217	GRCh38.p7	6:125052517	TACTGGCATTTCCAT[G/T]CAGGGAAGAGATCCC	154214
rs113973870	snp	A/G	0.0146672	0.084371	intron-variant	RNF217	GRCh38.p7	6:125031719	AGCTAGTCTCTAGGA[A/G]GTTCCAAACTTTCCC	154214
rs114084797	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087660	TTTAAATTTGGGAGG[A/G]ATCAGAAGCTAAAGA	154214
rs114103798	snp	A/G	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:124983600	TTTCATAAGGGTGTG[A/G]GGGAGATACCTAACG	154214
rs114121932	snp	C/G	0.0490535	0.14873	intron-variant	RNF217	GRCh38.p7	6:125046510	TCCAAATTTTTGAGC[C/G]TCACCAGGTGACTAA	154214
rs114124269	snp	G/T	0.00835141	0.0640778	intron-variant	RNF217	GRCh38.p7	6:125020682	TTGGCTTGTCTTGTT[G/T]GAAACTATTTTTACC	154214
rs114157995	snp	A/G	0.00914312	0.0669923	intron-variant	RNF217	GRCh38.p7	6:124965937	TTTAGCATCTACAGC[A/G]TTGTCTGGTATATAA	154214
rs114218180	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125023107	AAGCACAGGTTGCTA[C/T]AGGAGCAAGTCTTGT	154214
rs114229877	snp	G/T	0.029116	0.117091	downstream-variant-500B	RNF217	GRCh38.p7	6:125092789	ATTCAAGGGTGTGCT[G/T]TTGGGAAGGTGGATT	154214
rs114263817	snp	A/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125014772	ATTTTTGTGATGAAA[A/G]GAAGTTATTTTTAAA	154214
rs114280978	snp	A/T	0.0130921	0.0798413	intron-variant	RNF217	GRCh38.p7	6:125070839	GATTTTATCTAGAGT[A/T]AAATATTTGTTGGGG	154214
rs114323274	snp	A/G	0.0256215	0.110247	intron-variant	RNF217	GRCh38.p7	6:124985316	ATTTTTAATTTTTGC[A/G]GATACATAATAGGTA	154214
rs114328143	snp	A/G	0.0298908	0.118541	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089661	GAAAGAAAAAGGGAG[A/G]GACAGACTTGAGTGT	154214
rs114333876	snp	A/G	0.00914312	0.0669923	intron-variant	RNF217	GRCh38.p7	6:124986840	ATAAAGTATCTTGAA[A/G]TTTGTAATATAGATT	154214
rs114345326	snp	C/T	0.00636936	0.0560724	intron-variant	RNF217	GRCh38.p7	6:124979928	TCTCATGTCCTGTCA[C/T]TTACTGGATCTTTGC	154214
rs114391862	snp	A/T	0.0322114	0.122752	intron-variant	RNF217	GRCh38.p7	6:125064729	TATATTTAATATTTT[A/T]AAATGAGGACAAAAT	154214
rs114407343	snp	C/T	0.0142736	0.0832652	intron-variant	RNF217	GRCh38.p7	6:124976036	TATATTCCATGTGTC[C/T]TCAAGTGTTGGTGCT	154214
rs114415389	snp	A/T	0.00676609	0.0577691	intron-variant	RNF217	GRCh38.p7	6:124966249	GTGTCAATTCTATGG[A/T]CCCTCTACTCAAAGG	154214
rs114449532	snp	C/T	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:125069287	ATCAGCATCTATTTA[C/T]TTTTGCAGCATAGTC	154214
rs114504717	snp	C/G/T	0.0349115	0.127424	intron-variant	RNF217	GRCh38.p7	6:125048891	TTATGTTCTGAACAT[C/G/T]GTCAAACTCATACTA	154214
rs114518620	snp	G/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125018210	TTATATCTGTATCTT[G/T]TACAGTGTTTTAAAT	154214
rs114525335	snp	A/G/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125004864	CTTTCTAAAGGCCTT[A/G/T]TCTTAGTCCATTTTT	154214
rs114569448	snp	C/T	0.0193772	0.0965046	intron-variant	RNF217	GRCh38.p7	6:125025802	AGGAAGGAAGGGATA[C/T]TTACAAATGTACTCT	154214
rs114575819	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124976302	TTTCCTCCCTTCCTC[A/C]CTGTCACCTGGGCTG	154214
rs114632036	snp	C/G	0.0310518	0.120672	intron-variant	RNF217	GRCh38.p7	6:125014111	TGCTGTTTGCTTAGA[C/G]AACCTCAGGTAGCAC	154214
rs114680629	snp	A/G/T	0.0111256	0.0738101	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092350	AATTTCCGACTTTTC[A/G/T]TAATGTCCCAATGAC	154214
rs114698555	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125008711	CAGCCCCAGCTTGTA[C/T]CTATCTGGTCCTTTC	154214
rs114722264	snp	C/T	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:125000734	ATTTTAAGGAAGTTT[C/T]CCATATTCCTATTTC	154214
rs114763396	snp	A/C	0.0111196	0.0737302	intron-variant	RNF217	GRCh38.p7	6:124986933	ATTAATGTTTCCTGT[A/C]ATCAGTGTTAATTGT	154214
rs114889897	snp	A/G	0.0107246	0.0724382	intron-variant	RNF217	GRCh38.p7	6:125043412	AGGTCTGAGATTACT[A/G]TACTTCTCCTGAAAA	154214
rs114893014	snp	C/T	0.0111196	0.0737302	intron-variant	RNF217	GRCh38.p7	6:124977611	TCTAAATGGATTTGA[C/T]AGAGCTCTGTTGGTT	154214
rs114898631	snp	A/T	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982599	ACATAATAACTTATA[A/T]TCATTGCCGTTTTAT	154214
rs114902474	snp	A/G	0.0209421	0.100162	intron-variant	RNF217	GRCh38.p7	6:125053730	ATAGCACAGATTTCT[A/G]GTAAAACTAAGGGTA	154214
rs114902786	snp	C/T	0.0193772	0.0965046	intron-variant	RNF217	GRCh38.p7	6:125026550	AGAGCGTAAACGTGT[C/T]ATCAGTACTCCACAT	154214
rs115011867	snp	A/G	0.0364509	0.129988	intron-variant	RNF217	GRCh38.p7	6:124998753	CTGCAGTGAGCCATC[A/G]CACCACTGCACTCCA	154214
rs115035779	snp	C/G	0.0126979	0.078662	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081733	CTGTGATTCATGTAC[C/G]TTATAAAGCATTATT	154214
rs115043393	snp	C/T	0.00636936	0.0560724	intron-variant	RNF217	GRCh38.p7	6:125002018	ATTCTCCATATGAAA[C/T]AAGATCTTTAGTTAC	154214
rs115077325	snp	C/T	0.084728	0.187577	intron-variant	RNF217	GRCh38.p7	6:125027352	TCTACTCTCTATGTC[C/T]GTGAGTTCAATTGAT	154214
rs115085068	snp	C/T	0.0460142	0.144533	intron-variant	RNF217	GRCh38.p7	6:125065527	ACACTCCAGCAACAA[C/T]TAAATTCTGAAGCGT	154214
rs115215221	snp	G/T	0.0569829	0.158885	intron-variant	RNF217	GRCh38.p7	6:125042927	CAGAAATGTACTGCT[G/T]CCCAATAACAAGTGC	154214
rs115231673	snp	C/T	0.00597247	0.0543191	intron-variant	RNF217	GRCh38.p7	6:125070033	TTCCTAGTCCCCAAA[C/T]TTCATGAGATCATCT	154214
rs115256854	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:124973070	GTAGGAGCTAATATC[A/G]TCAATATGTAAACTA	154214
rs115262945	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125005918	ATAGTATTTAAAATT[C/T]AGATAAAAATCATTT	154214
rs115275795	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124988135	GAACTGCACATGCGA[A/G]GGATCTGGGTTGCAC	154214
rs115288836	snp	G/T	0.0626037	0.165477	intron-variant	RNF217	GRCh38.p7	6:124991006	CAGGATTTTGAGGTT[G/T]CAGTGAGCCAAGATC	154214
rs115316823	snp	C/T	0.021333	0.101051	intron-variant	RNF217	GRCh38.p7	6:125058490	GGCTTTGAATCCTTG[C/T]GATCTTTTGCTTTTC	154214
rs115318654	snp	A/G	0.0505692	0.150756	intron-variant	RNF217	GRCh38.p7	6:124992420	CTAAGAGGCTATAGA[A/G]CATTGATTTTAAGAA	154214
rs115349104	snp	C/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125013531	AGGTACCACAGCCCT[C/G]AGGCCAGAATATGTC	154214
rs115368195	snp	A/G	0.0126979	0.078662	intron-variant	RNF217	GRCh38.p7	6:125017853	GGGTTAACATATGCA[A/G]TGGTGAAAGGTCAAA	154214
rs115501550	snp	A/G	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:125005038	AGGGCAAGCCAGGGT[A/G]CCAGGCAGAAAGGGA	154214
rs115510509	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124976287	TCCCGCTCTCTCTCC[C/T]TTCCTCCCTTCCTCC	154214
rs115574287	snp	C/T	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:124999178	CCCCTAGTCCAGTTC[C/T]GAGACTGGCTGATCT	154214
rs115583903	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125049088	GACGTCAGCTTCCAA[C/T]TAGAAATCTAATTTC	154214
rs115643950	snp	A/T	0.0107246	0.0724382	intron-variant	RNF217	GRCh38.p7	6:125015081	ATAGACTTCCACCTA[A/T]CACTTAGCAATCACT	154214
rs115662489	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125029671	TTGTTGGTAAAAATG[A/T]AGAACGTGCATTTTT	154214
rs115704502	snp	C/T	0.0023933	0.0345097	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009528	CTATATCAATGTACT[C/T]ATTTATTATGATGAT	154214
rs115840095	snp	A/G	0.0498117	0.149749	intron-variant	RNF217	GRCh38.p7	6:125048608	ATTATGGCTTTTGCT[A/G]TCAATTCAACTGTTT	154214
rs115878995	snp	C/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:124970551	GATGTGCCTTTTAGA[C/T]ATTCATGAAGGGATG	154214
rs115881393	snp	A/G	0.0014654	0.0270287	intron-variant, missense	RNF217	GRCh38.p7	6:125082478	ACTTACTGGAACCTC[A/G]TAAGTGGTAGAACCA	154214
rs115882461	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125052753	TCTCATCTTCAAGAA[A/G]AGCATCTTCAGTTTT	154214
rs115984671	snp	C/T	0.0138799	0.0821421	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124960962	GGTCAGACCGATAGA[C/T]GACATGGCATTTAGA	154214
rs116028008	snp	C/T	0.0260105	0.111035	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086091	TTGCATGAACATATC[C/T]ATAAGGTTGTACATT	154214
rs116037547	snp	A/T	0.0166325	0.0896639	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961908	CTCAGGGTGTGCGTG[A/T]GTGTGTGCGCGGGTG	154214
rs116044830	snp	A/G	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:124994719	TCTTTTGTGCTAGTA[A/G]GTGCTACTTTAGGCA	154214
rs116066563	snp	C/T	0.00676609	0.0577691	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085845	ACAAATAGAAAAATA[C/T]TCTTACTGTGCTGTG	154214
rs116093334	snp	A/G	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:125036660	GAATCTACAAGTAAC[A/G]TAAACATATTTACAA	154214
rs116133376	snp	A/C	0.00597247	0.0543191	intron-variant	RNF217	GRCh38.p7	6:125061705	TAAATATGTTATTCT[A/C]TTTCTTTGTGGTCAA	154214
rs116164916	snp	C/T	0.029116	0.117091	intron-variant	RNF217	GRCh38.p7	6:124969660	TAAATACTTATTACA[C/T]ACAAGGCACTGTTTT	154214
rs116204911	snp	A/C	0.0107246	0.0724382	intron-variant	RNF217	GRCh38.p7	6:125050473	CTTTTTTTCTTTCTT[A/C]TAAACCCTCTGAGTA	154214
rs116255530	snp	A/G	0.0170251	0.090679	intron-variant	RNF217	GRCh38.p7	6:124979111	TATCCAGAGCTGGCA[A/G]TTTCGTTTTCAGGCT	154214
rs116290201	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125052951	TCCATTTATTGTACA[C/T]TTAGCAAGGATCAGG	154214
rs116306887	snp	A/G	0.0154538	0.0865337	intron-variant	RNF217	GRCh38.p7	6:125029665	TAAATGTTGTTGGTA[A/G]AAATGTAGAACGTGC	154214
rs116377893	snp	C/G	0.00393558	0.0441849	missense, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963149	CTCCCAGCACCCGCT[C/G]TTCCTTCCCCAGCCC	154214
rs116403810	snp	A/G	0.0685596	0.171987	intron-variant	RNF217	GRCh38.p7	6:125026781	GACCCTGTGGAAGAC[A/G]AGTGGGGTGTGAAAT	154214
rs116503844	snp	C/T	0.0498117	0.149749	intron-variant	RNF217	GRCh38.p7	6:124995215	TTTTGTGAAATATTA[C/T]ACATACAAAAGAATA	154214
rs116513403	snp	A/G	0.00914312	0.0669923	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085462	CTAAGTTTCATCAAG[A/G]TCTTAAAAAGAGAGA	154214
rs116592234	snp	C/T	0.003364	0.040874	synonymous-codon, nc-transcript-variant	RNF217	GRCh38.p7	6:125076686	AACTGAAGGATGTGA[C/T]CATATGACCTGCTCA	154214
rs116620995	snp	A/G	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:125026620	GGGAAGATAACTTTG[A/G]AACAAGTATTTAAAA	154214
rs116622335	snp	C/T	0.0126979	0.078662	intron-variant	RNF217	GRCh38.p7	6:125019692	CATTTTTTTCCTTCT[C/T]ACAGGCACACTGTCT	154214
rs116624634	snp	A/C	0.00914312	0.0669923	intron-variant	RNF217	GRCh38.p7	6:124977813	ATCTCATCACCTCTT[A/C]TGAAAAAACAAATTG	154214
rs116792511	snp	A/C	0.00755907	0.0610114	intron-variant	RNF217	GRCh38.p7	6:125063778	CATTTCAAGATGCAG[A/C]ACCAGTTTCAGAGAG	154214
rs116796717	snp	A/G	0.0170251	0.090679	intron-variant	RNF217	GRCh38.p7	6:124987733	CTCCTGCCTCAACCC[A/G]TGGAATAGCTGGGAC	154214
rs116812086	snp	A/G	0.0119091	0.0762411	intron-variant	RNF217	GRCh38.p7	6:125029775	TAAGTAGTTTTGAAG[A/G]TGAAAAGTTTTGGAA	154214
rs116879009	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124984355	TGTTCGACAGCAACC[C/T]GGGCAACATAGAGAA	154214
rs116933621	snp	A/C	0.00597247	0.0543191	intron-variant	RNF217	GRCh38.p7	6:125042993	GACTTGAAAGAAACT[A/C]TCTCTCACATTCTGA	154214
rs117176495	snp	A/G	0.0225045	0.103662	intron-variant	RNF217	GRCh38.p7	6:125000484	TTCAGCCATTTTTAT[A/G]TGATATAATATTCTA	154214
rs117176638	snp	C/T	0.0543475	0.155628	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045784	GACTTGATTTTTTTT[C/T]CAGTGGTCCCAATGT	154214
rs117188038	snp	A/C	0.0111196	0.0737302	intron-variant	RNF217	GRCh38.p7	6:125032812	GATAGTAAGGAGGGA[A/C]GAAAAGTTTAAGTAA	154214
rs117204930	snp	C/T	0.0103295	0.0711199	intron-variant	RNF217	GRCh38.p7	6:124989306	TTTGCCATGTAATTA[C/T]GTAGCAAAATAATCC	154214
rs117240492	snp	C/T	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:124976986	TTTCCTGATACTTTG[C/T]TCGTTTTTTTGTTTG	154214
rs117395327	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125075528	ACAAAACTATCAGAA[C/T]TTCTGAGACTCACTC	154214
rs117418347	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125064947	TTCTGAATATAACCA[A/G]TCTCATCAATTTACA	154214
rs117468662	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125025001	AAATGCAACCTCAGA[G/T]ACTCAGGAAGCCTTA	154214
rs117471250	snp	A/G	0.00439822	0.046688	intron-variant	RNF217	GRCh38.p7	6:125051441	TTACATTTCTTATCT[A/G]CCACCCTCTGTGCTA	154214
rs117542700	snp	A/G	0.417521	0.185571	intron-variant	RNF217	GRCh38.p7	6:125019831	TGTCCCCTTTTTTGC[A/G]GTGGGGGGGGAGTGA	154214
rs117564762	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125015117	GTTTCATTGATACCA[A/G]TGTGTATGCTATCTG	154214
rs117576321	snp	A/C	0.0119091	0.0762411	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088637	GCTAGAGAAGTGACT[A/C]TTTTAGAATAACAGT	154214
rs117608130	snp	A/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125002102	TGGTATTGTTAGAGA[A/G]TAAAATACTGGAGAG	154214
rs117608432	snp	C/T	0.00398564	0.0444627	intron-variant, upstream-variant-2KB, downstream-variant-500B, synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124964841	TCCAAAATATAAGCC[C/T]GCCTCCAGGGAAGTC	154214
rs117624987	snp	A/G	0.00676609	0.0577691	intron-variant	RNF217	GRCh38.p7	6:125005704	CATGTACCATATTAC[A/G]TTCGAAATATGATTT	154214
rs117846937	snp	A/T	0.00716266	0.059414	intron-variant	RNF217	GRCh38.p7	6:125054955	ACTCCATGTGGTGGG[A/T]ATGTGGTTGTGAGAT	154214
rs117933340	snp	C/G	0.0295035	0.117819	intron-variant	RNF217	GRCh38.p7	6:125043504	GTACCTAGCCCGTAC[C/G]TGCCTCAGAATTGTG	154214
rs117981213	snp	C/G	0.416218	0.186739	intron-variant	RNF217	GRCh38.p7	6:124976290	CGCTCTCTCTCCTTT[C/G]CTCCCTTCCTCCCTG	154214
rs117992230	snp	C/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:124972705	TTTCTTTCCTTGCTG[C/T]CCTAACTCTCTTTGC	154214
rs118000331	snp	A/G	0.040671	0.13668	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086671	GGGTCAAACCTTTTG[A/G]TACAAGCAACATCTT	154214
rs118003895	snp	C/T	0.0182019	0.0936463	intron-variant	RNF217	GRCh38.p7	6:125002599	CGACCACAGCCACCC[C/T]GTTTTCCTCTTCTTG	154214
rs118078766	snp	A/G	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125023497	TAAAGTAGTACAGCC[A/G]TTACAGAAGACAGTA	154214
rs118094755	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125068916	GGAAGGATTTAGTAG[A/G]ATGACATGTATAATC	154214
rs118104622	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125039645	ATTAACAGAATATAC[A/G]TTTGTCTCAGTGCCA	154214
rs118106888	snp	C/G	0.0103295	0.0711199	intron-variant	RNF217	GRCh38.p7	6:124984181	CAAATTACTGGAACA[C/G]AGAAAAGTGCTAATA	154214
rs118124979	snp	A/G	0.0248432	0.108648	intron-variant	RNF217	GRCh38.p7	6:124969612	TAAACATTCTTACAT[A/G]TATTTTTATTTAATT	154214
rs137872706	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124984992	AAGACAAAGCACCCA[A/G]TAGAAAAGAAATGCA	154214
rs137897191	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124998517	TAAAAACTGTGTAGA[A/T]GGCCAGGTGCCGTGG	154214
rs137942083	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125031039	ACATGCACGCGGAAC[A/G]CCACATGGAAGCTGT	154214
rs137981529	snp	G/T	1.67094e-05	0.0028904	missense, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081475	TAATTATGGTTTTGG[G/T]ATTGGCACTAGGGGC	154214
rs138003856	snp	A/T	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:125065737	TTAGTTTCCATTTTC[A/T]TTTCTTTTCAGGTTT	154214
rs138004047	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125023227	AAAAATATGTGTAAA[A/G]TATGTCCTGGGTAGA	154214
rs138013458	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089531	CATTGAATGTAACTG[A/G]TATTAACCCTATTCT	154214
rs138016792	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124979508	AGATACCAGCGTGGC[A/G]CAGAGCACCAAAGGC	154214
rs138093458	in-del	-/G	0.47726	0.104176	intron-variant	RNF217	GRCh38.p7	6:125066995	CAGTGGAATGTTGCA[-/G]GGAGTATTATACGAG	154214
rs138119645	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125017654	GCTCAAGTCTTATAA[A/C]CCTATCATTAAAATA	154214
rs138125920	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125017064	CCTTTTCTCTTTGCT[G/T]CTTTTCCCTTTTGCT	154214
rs138141789	snp	G/T	0.0119091	0.0762411	intron-variant	RNF217	GRCh38.p7	6:125028315	CAAAGATAATTTGAG[G/T]ACCCCAAGATAGGAG	154214
rs138223947	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124971317	ACTTAATTACATGTT[A/T]TGAGGAAGCGAAAGG	154214
rs138246230	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125044531	GTCCTTTGAATACAT[A/T]AATTTTGTAAATTAC	154214
rs138267127	snp	A/G	0.00636936	0.0560724	intron-variant	RNF217	GRCh38.p7	6:124978967	AATGGGGGAATGCAA[A/G]CTGATTGGTCCATGG	154214
rs138293014	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125037562	AGCACTAAGCCCTGT[A/G]GTTGCTGCTGAGTAA	154214
rs138330071	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967149	ACATAAATCTGGAAC[A/G]TTCATTTCAGAAGTA	154214
rs138383480	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125000381	ACACTTTGAGAAACA[C/T]ACATAATGTTATATG	154214
rs138385815	snp	A/C	0.0103295	0.0711199	intron-variant	RNF217	GRCh38.p7	6:125049885	ATGGAAAATTAGTTC[A/C]GTTTGAAATATGTTG	154214
rs138388970	snp	C/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125066524	TTCTTACCACAGATG[C/T]GTGCACTGCCAGCTC	154214
rs138399120	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124990206	TTTGTTGTTAATTAA[C/T]CTCCTTCTGAATTAC	154214
rs138414087	snp	A/G	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961023	GCCTCAGACACACAT[A/G]TATGATGGAAATGTT	154214
rs138434664	in-del	-/TAGAG	0.235564	0.249583	intron-variant	RNF217	GRCh38.p7	6:124980695	TTCTTTGTTTTTGGT[-/TAGAG]TAGAGTGATAAAGTA	154214
rs138476704	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125071148	TACTATTTTCTTCAT[A/G]CAGATGGTTCCCAAG	154214
rs138485712	snp	A/G	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:124993503	TCATTCCTCAGTTGC[A/G]CAAATATTCACTGAG	154214
rs138498007	snp	A/C	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125006962	CTCAAAAAAGAAAAA[A/C]AGAATGCATGATAGA	154214
rs138510845	snp	A/G	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:124993088	TTTTGTAATAATTGA[A/G]TTCAAATAGTAAAAT	154214
rs138598871	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125029852	CTGTGAATTAGCTGA[G/T]ATGACGACAGCACTG	154214
rs138609048	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125062032	CTCTAAATTATATCT[A/T]AAATTACAATATCTT	154214
rs138633589	snp	C/T	0.0513262	0.151752	intron-variant	RNF217	GRCh38.p7	6:125051920	AGTGAAGAAATGGGT[C/T]CTCGGACAAGAAATA	154214
rs138715759	snp	A/G	0.0142736	0.0832652	intron-variant	RNF217	GRCh38.p7	6:125030891	CCACATTTTCCTCCC[A/G]CACTGCCCTAGCAGA	154214
rs138716536	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124980495	TGTTGAATTGTTTTG[G/T]ATAAGTCATTTGCTT	154214
rs138729612	in-del	-/AAAAC	0.231775	0.249335	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961223	CCTCTCAGGAGAAAA[-/AAAAC]AAAACAAGGGCTGGC	154214
rs138755152	snp	A/C	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125054366	AAGGGCAGGAAAATA[A/C]TCTCTGCAGCTGCCC	154214
rs138764964	snp	C/T	0.00874735	0.0655527	intron-variant	RNF217	GRCh38.p7	6:124975012	AATTCTGGGCTTTTT[C/T]ATTCATGTGAATGAC	154214
rs138793773	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:124974626	ATTACAGCTTCAGCT[A/G]TAGTTAAAATATTTG	154214
rs138798715	snp	A/G	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:125040938	AGGTATTGATGGAAT[A/G]TATCTCAAAATAATA	154214
rs138817676	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125012668	CTTTGGTGCTCCTTA[A/G]CATAATATGGTAGCA	154214
rs138827013	snp	G/T	0.0142736	0.0832652	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971714	CTGCCTCGGCCTCCC[G/T]AAGTGCTGAGATTAC	154214
rs138857014	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124983935	GAGGGCCTGTTCCTC[A/T]TGCATGGCACCTTCT	154214
rs138909484	snp	C/T	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:124995101	TTGAGTAGGGAGATG[C/T]TTGTGGTTTGTCAGT	154214
rs138920138	snp	A/G	0.00307051	0.0390618	intron-variant	RNF217	GRCh38.p7	6:125076907	TGGGAATTAAGTAGT[A/G]AAAATAGAACTTGGA	154214
rs138971876	snp	A/C	0.00953873	0.0683987	intron-variant	RNF217	GRCh38.p7	6:125071454	CATTTTCAACCTATG[A/C]TATTTTCAACTTGGA	154214
rs138988779	snp	A/G	0.00176202	0.0296295	missense, utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125082926	CGATCACGGACAGGT[A/G]TGCACTGGTAACATG	154214
rs139010277	snp	A/G	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:125037192	TGCCACTGTCACACT[A/G]ATGTAATTCCTATAG	154214
rs139013106	in-del	-/ATAGGGTCAGATAGT	0.00676609	0.0577691	intron-variant	RNF217	GRCh38.p7	6:124979657	TGACTTACAAAGGTA[-/ATAGGGTCAGATAGT]ATAGATCCTCCATGG	154214
rs139054297	snp	G/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125047424	TTGAGAGTGAAATAT[G/T]TAAAAATTGACAAAT	154214
rs139089461	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124972952	TTGATGCATGTAAAG[A/G]CATTATTAATCTGTT	154214
rs139135790	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086893	GTCCCAAGGCTCCAA[C/T]TGAGCCTTTATCTTT	154214
rs139142227	in-del	-/AATG	0.366473	0.221211	intron-variant	RNF217	GRCh38.p7	6:124977446	CAAAGATTATAAAAT[-/AATG]AAGCCAGTTCTAAAA	154214
rs139153998	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, missense	RNF217, RNF217-AS1	GRCh38.p7	6:124963925	AAATGTATCCCTTGG[C/T]CTTTGCCTACTTTTC	154214
rs139174573	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125052447	CTAAGGCAAGGATCA[C/T]TTGGCCACATTTGGA	154214
rs139174695	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125002635	AATTGTCAGTGTCAC[A/G]CTGGCCCCGTATGTT	154214
rs139179532	in-del	-/TG			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124968334	TGTGTGCAAAATGTA[-/TG]TGTGTGTGTGTGTGC	154214
rs139194543	snp	A/G	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:124969363	TACTTAAAAATGTTT[A/G]TTTTTTTCAAATTCA	154214
rs139198726	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045686	TAATCTAGTAACCTT[A/G]TAGGAAGGCTGATCT	154214
rs139232420	snp	A/G	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:125030075	AGCAAGAGAAAATGA[A/G]GAAGAAGCAAAAGCA	154214
rs139252852	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125013732	CAATTACATCCCAGT[C/T]ATTCATTGTGTCATC	154214
rs139265718	snp	A/C	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125069213	GAGACAATTATTGCT[A/C]TCAGAGTGTTGGCCT	154214
rs139268641	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-3-prime	RNF217, RNF217-AS1	GRCh38.p7	6:124964612	AGTCCCTAACTAAAA[A/G]TGCAAACAAAGACTT	154214
rs139291324	snp	G/T	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967802	TTTTTTTCTTTGAGA[G/T]AATCTCCCTCTTGTC	154214
rs139319831	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125010104	TCTTCAGGGTGTACT[C/G]CCTGTTCTCTGCATT	154214
rs139405622	snp	G/T	0.00874735	0.0655527	intron-variant	RNF217	GRCh38.p7	6:125019541	CCTAAATTTTCCCCT[G/T]TTTATTTTTTAGCTT	154214
rs139408927	snp	C/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124978246	TCACCAGTCAGAAAT[C/G]TCTTTGGCCACTGCT	154214
rs139441405	snp	C/T	0.00438332	0.0466095	intron-variant	RNF217	GRCh38.p7	6:125055469	TTCATTAGAGATTCA[C/T]AAATGTGATAGTTCA	154214
rs139473463	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125058329	ATTTAAGGAGGCCAC[A/G]TATAAATATTGACTT	154214
rs139513719	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125014307	AGTTTGTACTGCTCT[A/G]AATTCCAGGCTGTAC	154214
rs139541817	snp	A/G	1.65748e-05	0.00287874	stop-gained, nc-transcript-variant	RNF217	GRCh38.p7	6:125057971	CTGCCAATTCGTCTG[A/G]TGTTTTAAGTGCCAC	154214
rs139569888	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125074981	GAGCATTTTCAATAA[A/G]ATTTCTAAGCAAAGA	154214
rs139617496	snp	A/G	0.00163055	0.0285065	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009285	GAAAGGGATGAAGGT[A/G]AAGTACATAGATGAA	154214
rs139664635	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124990863	TGAGGCCAGGAGTTC[A/G]AGACCAGCCTGAGCA	154214
rs139668346	snp	C/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:124987612	AAATTAGTGTGAAAA[C/T]GGAGATCTTGCTTCT	154214
rs139701267	snp	A/T	0.00716266	0.059414	intron-variant	RNF217	GRCh38.p7	6:125034365	TTCATCTTGAATTAA[A/T]TTTTGTATAAGGTGT	154214
rs139716209	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125063231	GTTTCTAAGTCAAAA[A/C]TTAAAAGTGAGATGC	154214
rs139746353	snp	A/G	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125074145	AAGTCCTGCCAGCCA[A/G]TTGACAAACTTTTCT	154214
rs139765938	snp	C/T	0.00676609	0.0577691	intron-variant, utr-variant-5-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:124996646	TTGTGTAACCTGAAG[C/T]ATATACAGTGTGAGC	154214
rs139819003	snp	A/T	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:124995451	AGTTGTGCACATTTT[A/T]AATCACTTTTATAAA	154214
rs139842242	snp	A/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125058750	GGAAGACTCTCCTAC[A/G]GGAGGTCAGCCAGTA	154214
rs139855127	snp	A/C	0.00795532	0.062565	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089888	TTGTATTGTTTCAAG[A/C]CACTAGTATCTAAAT	154214
rs139888335	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084363	ACAAGTAACTAGACT[A/G]TGATATGCCTTTGCT	154214
rs139888829	snp	C/G/T	0.00716266	0.059414	intron-variant	RNF217	GRCh38.p7	6:124991828	ATTTAGTTCCTCAGT[C/G/T]CTAGTAGCAACTTTT	154214
rs139888853	snp	C/T	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:125041229	AAATCTCATTGATTC[C/T]ACTTCCAAAATACAC	154214
rs139904922	snp	A/G	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:124972515	TTTAAACTTTATAAC[A/G]GTATCTCATGTCCCT	154214
rs139928698	snp	C/T	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:125047278	TTTAAATGTGTTGTT[C/T]TTATGAAATGGGTAA	154214
rs140064999	snp	G/T	0.00478085	0.0486577	intron-variant	RNF217	GRCh38.p7	6:125068449	AAGCTCATCTATTGA[G/T]TACTGTCTTCATACT	154214
rs140065066	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125025082	AAGTCAGGAAAATCA[A/G]GAATGTGATGTGCTA	154214
rs140086309	in-del	-/AGGG	0.209997	0.246779	intron-variant	RNF217	GRCh38.p7	6:125025576	GGAAGAAAAGAAGGA[-/AGGG]AGGGAGGGAGGGAGG	154214
rs140100167	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125070936	CTTGGTGAAACTGGA[A/G]ACAAATACTTGTGGG	154214
rs140137243	snp	A/C	0.00597247	0.0543191	intron-variant	RNF217	GRCh38.p7	6:125030052	AAAGGCATTTCTTAC[A/C]TGGCAGCAGCAAGAG	154214
rs140168996	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125055542	TTTATAGAGCGAATC[C/T]GAGTTTCAAAGCATC	154214
rs140177984	snp	C/T	1.66316e-05	0.00288367	synonymous-codon, nc-transcript-variant	RNF217	GRCh38.p7	6:125057965	CCCTACCTGCCAATT[C/T]GTCTGGTGTTTTAAG	154214
rs140213445	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124997976	CCTGAATGTCTGCCT[G/T]ACTCCGGCATTCCTT	154214
rs140246676	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124993111	AGTAAAATATACTTG[A/G]TATATGAACTTTCTT	154214
rs140246907	snp	A/G	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125042665	GTTGGATGGTATCCC[A/G]ATGTGGTTGATTAAC	154214
rs140268831	snp	C/G	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:124976609	CTTCATAGTGATTCT[C/G]TTGCCTCAGCCTCCC	154214
rs140319300	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125039420	CTAAATATATATGCA[A/C]CCAATACAGGAGCAC	154214
rs140334377	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124973302	CTCATGGTTAATTTC[A/G]CTTCACTGACTCAGT	154214
rs140334513	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125023681	ACCACCTAAGTGCCC[A/G]TTGATAGATGAGTGG	154214
rs140379969	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124979093	CACTCTGGTCATTGA[C/T]TCTATCCAGAGCTGG	154214
rs140414860	snp	A/T	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125027033	CATTTTTGTGGGTAC[A/T]TAGTAGGTGTATATA	154214
rs140470814	snp	C/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:124978749	CAGCTCATTTGTTCT[C/G]ACTGCCCACAGCTTG	154214
rs140487823	snp	G/T	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:125016388	GGGATATACTAAAGC[G/T]GTGTTTTGAATTGAG	154214
rs140521257	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125056714	AGTGACGTGACATAG[A/C]GGAGCAAAGAGAGTG	154214
rs140531000	snp	C/T	0.00676609	0.0577691	intron-variant	RNF217	GRCh38.p7	6:124974880	ATGTTTCCAGAAGCA[C/T]AGATGTTGTCCTCGA	154214
rs140534966	snp	G/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125025877	CTGTTGGATTTTTAT[G/T]CTGTCAAGTACAAGG	154214
rs140584094	snp	C/T	0.0103295	0.0711199	intron-variant	RNF217	GRCh38.p7	6:125038840	TTTTTTCTAATTTAA[C/T]TTTTAAGTTCTGTGA	154214
rs140596835	snp	C/T	0.00517822	0.0506191	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085099	ATACATATATACCAA[C/T]GGGCTGAATAACATA	154214
rs140610507	snp	C/T	0.0433465	0.140692	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982013	ATCCTGGCAACAGAG[C/T]GAGACTCTGTCTCAA	154214

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