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

RNF10

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs10056	snp	G/T	0	0	stop-gained, nc-transcript-variant	RNF10	GRCh38.p7	12:120576601	TCTGAAGAGAAAGGA[G/T]GAAAGAAAAGAAAAA	9921
rs10505	snp	A/C	0	0	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576998	CTGGGTTGGACTGCT[A/C]TAATGCATCTCAAAG	9921
rs488313	snp	C/T	0.0607341	0.163335	intron-variant	RNF10	GRCh38.p7	12:120573203	ccatattagatatta[C/T]tgtggcagtggaatt	9921
rs489854	snp	G/T	0.494272	0.053207	intron-variant	RNF10	GRCh38.p7	12:120567862	GCATTTCATTATGGg[G/T]gtgtgtgtgtgtgtg	9921
rs492574	snp	C/T	0.491525	0.0645418	intron-variant	RNF10	GRCh38.p7	12:120568155	TAGGCTCAAGCCATC[C/T]CCCCACCTCAGCCTC	9921
rs516479	snp	A/G	0.390838	0.206555	intron-variant	RNF10	GRCh38.p7	12:120568498	ACAGAGCTAGACTCC[A/G]TCTCAAAAAAAAAAA	9921
rs532725	snp	C/T	0.494442	0.0524218	intron-variant	RNF10	GRCh38.p7	12:120562271	TCTTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT	9921
rs533843	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120559271	actgcaacctccacc[C/T]cctcggttcaaacga	9921
rs541126	snp	A/G	0.302936	0.244331	utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534593	ACCGAGGACGAGGAG[A/G]CCGGGGCTCGGGAGT	9921
rs546417	snp	A/C	0.421593	0.181813	intron-variant	RNF10	GRCh38.p7	12:120566787	AAAAAAAATTGAATT[A/C]TGTAAATGGGTTTAC	9921
rs560385	snp	A/G	0.0607341	0.163335	intron-variant	RNF10	GRCh38.p7	12:120559891	taatagaaacagggt[A/G]tctctatgttggcca	9921
rs567156	snp	C/T	0.337614	0.234145	intron-variant	RNF10	GRCh38.p7	12:120566573	GGTTTCACCATGTTG[C/T]CCAGCCTGGTCTTGA	9921
rs568055	snp	A/T	0	0	intron-variant	RNF10	GRCh38.p7	12:120543244	CTGATATAACTATAC[A/T]AAAGTACCTGTCTGC	9921
rs568058	snp	C/T	0.0217236	0.101931	intron-variant	RNF10	GRCh38.p7	12:120566657	ctcccacctcagcct[C/T]ccgagtagccgggac	9921
rs574858	snp	C/T	0.398714	0.200958	intron-variant	RNF10	GRCh38.p7	12:120572893	aaaaaaaaggccagg[C/T]gcagtggttcatgtc	9921
rs585510	snp	C/T	0.391024	0.206427	intron-variant	RNF10	GRCh38.p7	12:120562330	ccgagatcacgccac[C/T]gcactccagcctggg	9921
rs603574	snp	C/T	0.393803	0.204501	intron-variant	RNF10	GRCh38.p7	12:120560640	TTTCAAATACAGCCT[C/T]TTCTCTGGGGTGAAA	9921
rs608724	snp	A/G	0.498734	0.0251279	intron-variant	RNF10	GRCh38.p7	12:120574045	GGGACCTAATGGGAG[A/G]TGTATGGGTCATGGG	9921
rs614053	snp	C/T	0.0607341	0.163335	intron-variant	RNF10	GRCh38.p7	12:120548950	gggcgcggtggctca[C/T]gcctgtaatcccagc	9921
rs614226	snp	C/T	0.296109	0.245711	intron-variant	RNF10	GRCh38.p7	12:120536707	TTAGAGTGGTCTGTT[C/T]AAAGCAATTGATAAG	9921
rs630654	snp	C/T	0.0614824	0.164198	intron-variant	RNF10	GRCh38.p7	12:120547574	aggtgtggtggctca[C/T]gcctgtaatcccagc	9921
rs651627	snp	A/G	0.389152	0.207694	intron-variant	RNF10	GRCh38.p7	12:120571395	TCAATTTGTCCAGCC[A/G]TATTAGAATGAGAGG	9921
rs787829	snp	C/T	0.49614	0.0437598	intron-variant	RNF10	GRCh38.p7	12:120545273	gcaagctctgcctcc[C/T]ggggttcacgccgtt	9921
rs787830	snp	C/G	0.378765	0.214288	intron-variant	RNF10	GRCh38.p7	12:120548388	gTCTGGATAAGAAAC[C/G]AGCAGAAGAGAGCAC	9921
rs787831	snp	A/G	0.382279	0.212137	intron-variant	RNF10	GRCh38.p7	12:120548939	cctcccaaagtgctg[A/G]gattacaggcgtgag	9921
rs787832	snp	A/G	0.335559	0.234904	intron-variant	RNF10	GRCh38.p7	12:120548998	attagggaaatgata[A/G]catgtctgtgctcat	9921
rs787833	snp	A/C	0.398354	0.201224	intron-variant	RNF10	GRCh38.p7	12:120549818	aataaataataaata[A/C]aAATTTAAAAAAGGA	9921
rs787834	snp	C/T	0.382279	0.212137	intron-variant	RNF10	GRCh38.p7	12:120550657	gctagagtgcagtgg[C/T]gtgatcttggctcac	9921
rs787835	snp	C/T	0.030278	0.119257	intron-variant	RNF10	GRCh38.p7	12:120550665	gcagtggcgtgatct[C/T]ggctcactgccagct	9921
rs787947	snp	C/T	0.498852	0.0239341	intron-variant	RNF10	GRCh38.p7	12:120568926	CATCAAAAAGTATCT[C/T]TCttggccaggtaca	9921
rs787949	snp	C/T	0.0204374	0.0990014	intron-variant	RNF10	GRCh38.p7	12:120560678	AACATTCAAAGCTCA[C/T]GATGGTGTAGCTAAA	9921
rs812018	snp	A/G	0	0	intron-variant	RNF10	GRCh38.p7	12:120550724	gcctcagcctcccga[A/G]tagctgggactatag	9921
rs1043097	snp	C/T	0	0	utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534781	CGCGCCCGCTCCGCT[C/T]CGACTGCCGTCGCCG	9921
rs1137266	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120567448	tggcttatgcctgta[A/G]tcccagcactttggg	9921
rs1137270	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120567519	CAGCCTGACCAACAC[A/G]GTGAAACCCTATCTC	9921
rs1137272	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120567543	ctatctctactgaaa[A/G]tgcaaaaattagcag	9921
rs1137273	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120567547	ctctactgaaagtgc[A/G]aaaattagcagggca	9921
rs1137274	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120567548	tctactgaaagtgca[A/G]aaattagcagggcat	9921
rs1137275	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120567608	tgggaggctgaggca[A/G]cagaattgcttgaac	9921
rs1167711	snp	C/G	0.49614	0.0437598	intron-variant	RNF10	GRCh38.p7	12:120551823	TTAAAGACtgtatta[C/G]tccattctctcattg	9921
rs1167712	snp	G/T	0.496649	0.0407971	intron-variant	RNF10	GRCh38.p7	12:120553653	catgatccacccgcc[G/T]cggcctcccaaagtg	9921
rs1167713	snp	C/T	0.398714	0.200958	intron-variant	RNF10	GRCh38.p7	12:120554210	atgcctggcctaatt[C/T]ttctatttttagtag	9921
rs1167714	snp	A/G	0.382473	0.212016	intron-variant	RNF10	GRCh38.p7	12:120555262	tcttggctcactgca[A/G]cctctgcctccaggg	9921
rs1167715	snp	A/G	0.398534	0.201091	intron-variant	RNF10	GRCh38.p7	12:120543668	ggactccaggcatat[A/G]caccattcttggctt	9921
rs1167716	snp	C/T	0.398534	0.201091	intron-variant	RNF10	GRCh38.p7	12:120543607	gccatgttgcccaga[C/T]gggtctcaaactcct	9921
rs1167717	snp	C/T	0.0197687	0.0974348	intron-variant	RNF10	GRCh38.p7	12:120542380	gatcacttgagtcca[C/T]gagtttgcgaccagc	9921
rs1167718	snp	G/T	0.498547	0.0269177	intron-variant	RNF10	GRCh38.p7	12:120541591	aaaaattagccaggc[G/T]tggtggcgggcgcct	9921
rs1167719	snp	C/T	0.382279	0.212137	intron-variant	RNF10	GRCh38.p7	12:120540936	CCCGGGAGGTGGAGG[C/T]TGCGGCAAGGCCGAG	9921
rs1167720	snp	C/T	0.382279	0.212137	intron-variant	RNF10	GRCh38.p7	12:120540898	CACTACACTCCAGCC[C/T]GGGCAACAAGAGCAA	9921
rs1167721	snp	C/T	0.382279	0.212137	intron-variant	RNF10	GRCh38.p7	12:120540015	GAAACCCATCTCTAC[C/T]AAAAATACAAAAATT	9921
rs1167722	snp	C/T	0.382279	0.212137	intron-variant	RNF10	GRCh38.p7	12:120539995	ATACAAAAATTAGGC[C/T]GGTGTGGTGGTGGAC	9921
rs1167723	snp	C/T	0.378765	0.214288	intron-variant	RNF10	GRCh38.p7	12:120539578	AGCTAGAAATGAAGA[C/T]GCCAAGTAATTTAAC	9921
rs1167757	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120543980	tcggcctcccaaagt[A/G]ctgggattacaggca	9921
rs1167758	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120543968	agtactgggattaca[A/G]gcatgagccaccatg	9921
rs1184538	snp	C/T	0.49614	0.0437598	intron-variant	RNF10	GRCh38.p7	12:120551380	gctcactgcaacctc[C/T]gcctctcgggttcaa	9921
rs1710138	snp	A/T	0	0	intron-variant	RNF10	GRCh38.p7	12:120538788	GGTATTATGAGGCAG[A/T]TATTTTGAGGTTGGT	9921
rs2280168	snp	C/T	0.241141	0.249849	intron-variant	RNF10	GRCh38.p7	12:120571155	TGATTATATTCGTCA[C/T]GTTCCAAGGGGTGTC	9921
rs2292680	snp	A/C	0.383439	0.21141	intron-variant	RNF10	GRCh38.p7	12:120575345	TCTTACTGAGACCCT[A/C]AAATTGGGAATTCCG	9921
rs2292681	snp	C/T	0.47201	0.114942	intron-variant	RNF10	GRCh38.p7	12:120557529	TGAAACATGGACACT[C/T]ATATGTAGCAGGGCA	9921
rs2673626	snp	G/T	0	0	intron-variant	RNF10	GRCh38.p7	12:120553557	acaaaattagccagg[G/T]ggtgggcgcctgtag	9921
rs2743850	snp	A/G	0.00636936	0.0560724	intron-variant	RNF10	GRCh38.p7	12:120567745	AAAGAAGGGAATGTA[A/G]TTCTTCTATTCACGT	9921
rs3049456	in-del	-/A/AA/AAA	0.444133	0.157519	intron-variant	RNF10	GRCh38.p7	12:120541437	aaaaaaaaaaaaaaa[-/A/AA/AAA]ggaaaaCTCAGGGGA	9921
rs3049489	in-del	-/T/TT	0	0	intron-variant	RNF10	GRCh38.p7	12:120541452	ttttttttttttttt[-/T/TT]gagacggagtctcac	9921
rs3049493	in-del	-/TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	0	0	intron-variant	RNF10	GRCh38.p7	12:120553069	TTTTTTTTTTTTTTT[lengthTooLong]GAGATGTAGTCTCGC	9921
rs3088345	snp	C/G	0.383439	0.21141	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577038	CACTGCTCTGCTGTA[C/G]CATCATGTCAGGGCT	9921
rs3168677	snp	C/G	0	0	intron-variant	RNF10	GRCh38.p7	12:120555146	TCAAAGTAGGCCTCA[C/G]CCTTGTGGCAGGGAG	9921
rs3203671	snp	C/T	0.00358779	0.0422022	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576719	ACAAAAGCATGGGGG[C/T]AAAAAAAACAAAAAC	9921
rs3213565	snp	A/G	0.390651	0.206682	intron-variant	RNF10	GRCh38.p7	12:120554598	GCAGCCCTGGTTCAT[A/G]AGGCACTGCACTAGG	9921
rs3817301	snp	C/T	0.136506	0.222754	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120576224	GCCACCCTGTACCAA[C/T]TCAAGATTCTAAAGG	9921
rs3817302	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120560530	TAAGAAATCTAAGAA[A/G]CCCAGAGATGTAGTC	9921
rs3999427	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120550770	ctaatttttttattt[G/T]tatttttagtagaga	9921
rs4102203	snp	A/G	0.121369	0.214369	intron-variant	RNF10	GRCh38.p7	12:120538568	GATATTTACTGCTGC[A/G]TGTTCTCAGAAATAC	9921
rs4347449	snp	A/C	0.334412	0.235318	intron-variant	RNF10	GRCh38.p7	12:120556414	cgggtacctgtagtc[A/C]cagctacttgggagg	9921
rs4766969	snp	A/G	0.393619	0.204631	intron-variant	RNF10	GRCh38.p7	12:120550435	TTGTTGACTGAGCAC[A/G]AGCTCTTAGATCTAA	9921
rs4767910	snp	C/T	0.39121	0.2063	intron-variant	RNF10	GRCh38.p7	12:120553437	AGACAAAGTCTTGCT[C/T]TGTCACCCAGGCTGG	9921
rs4767912	snp	A/G	0.393803	0.204501	intron-variant	RNF10	GRCh38.p7	12:120543399	GCTTATAATCCCAGC[A/G]CTTTGGGAGGCTGAG	9921
rs4767913	snp	C/T	0.243633	0.249919	intron-variant	RNF10	GRCh38.p7	12:120548412	AGAGCACAGTCAGGG[C/T]GGGAGGAAAATTGCT	9921
rs4767914	snp	C/T	0.391024	0.206427	intron-variant	RNF10	GRCh38.p7	12:120556014	GGCTTGTCTCAAACT[C/T]CCAGCTTCAAGTGAT	9921
rs4767915	snp	A/G	0.24449	0.249939	intron-variant	RNF10	GRCh38.p7	12:120561324	AGGAGTACCTGAAAC[A/G]GCAAGAATTACACAA	9921
rs5801387	in-del	-/T	0.42574	0.177808	intron-variant	RNF10	GRCh38.p7	12:120540131	TAGGAATTTATTATC[-/T]TTTTTTTTTTTGTAG	9921
rs5801391	in-del	-/T	0	0	intron-variant	RNF10	GRCh38.p7	12:120548676	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCGC	9921
rs7133978	snp	A/T	0.334871	0.235153	intron-variant	RNF10	GRCh38.p7	12:120559059	attaacttttaattt[A/T]aaattatttttttta	9921
rs7138112	snp	C/T	0.496105	0.0439572	intron-variant	RNF10	GRCh38.p7	12:120559934	actcctaacttcagg[C/T]gatccacctgcctca	9921
rs7299954	snp	C/T	0.256619	0.249912	intron-variant	RNF10	GRCh38.p7	12:120558790	ttggcaggctagtct[C/T]gaactcccgagctca	9921
rs7488320	snp	G/T	0.391024	0.206427	intron-variant	RNF10	GRCh38.p7	12:120543827	aaaaattagctgggt[G/T]tggtggtgcacacct	9921
rs7956232	snp	A/G	0.00795532	0.062565	intron-variant	RNF10	GRCh38.p7	12:120563751	TGGGCATGGGGAGGG[A/G]TGGGGAGCCTCCTGG	9921
rs7956884	snp	C/T	0.0566069	0.158427	intron-variant	RNF10	GRCh38.p7	12:120556361	aacacggtgaaaccc[C/T]gtctctactaaaaaa	9921
rs7956998	snp	A/G	0.337386	0.23423	intron-variant	RNF10	GRCh38.p7	12:120557129	CATACATGTACCTAC[A/G]TTGTAAACAATTTTA	9921
rs7961574	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120545435	ctgacctcgtgatcc[A/G]cccacctcggcctcc	9921
rs7962410	snp	C/T	0.254664	0.249956	intron-variant	RNF10	GRCh38.p7	12:120545436	tgacctcgtgatccg[C/T]ccacctcggcctccc	9921
rs7966798	snp	A/G	0.00676609	0.0577691	intron-variant	RNF10	GRCh38.p7	12:120541560	ctgcctcagcctccc[A/G]agcagctgggactac	9921
rs7970747	snp	A/G	0.0729998	0.176553	intron-variant	RNF10	GRCh38.p7	12:120542453	gccaccaagtccagc[A/G]CTGAAACTTTGCTTT	9921
rs7970776	snp	A/G	0.0729998	0.176553	intron-variant	RNF10	GRCh38.p7	12:120569027	ccaggctggagtgca[A/G]tagtgcaatctcagc	9921
rs7971844	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120542660	cgggttcaaatgatt[C/T]tcatgccttagcctc	9921
rs7972244	snp	A/G	0.337614	0.234145	intron-variant	RNF10	GRCh38.p7	12:120557069	GAATGGCGTGAACCA[A/G]GGAGATGGACCGTCT	9921
rs7973555	snp	G/T	0.269809	0.249214	intron-variant	RNF10	GRCh38.p7	12:120568824	gctgtgatgcattca[G/T]tagctcactgcagtc	9921
rs7973558	snp	C/T	0.00358779	0.0422022	intron-variant	RNF10	GRCh38.p7	12:120538742	ATCCCCCTGGGCCGA[C/T]AGAACTGCCAGGGAG	9921
rs9669663	snp	C/T	0.382279	0.212137	intron-variant	RNF10	GRCh38.p7	12:120557016	GAGCGTGGTGGCAGG[C/T]GCCTGTAGTCCCAGC	9921
rs9705874	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120557101	aaaaaaaaaaaaaaa[A/G]gaaaaaaaTGATCAT	9921
rs9706503	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120557102	aaaaaaaaaaaaaaa[A/G]aaaaaaaTGATCATA	9921
rs9888315	snp	C/G	0.335788	0.23482	intron-variant	RNF10	GRCh38.p7	12:120559216	AGACGGAGTCTTGCT[C/G]TGTTTCCCAGGCTGG	9921
rs10515974	snp	A/G	0.0755793	0.179102	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577365	ATCGAGCTTGTTTTC[A/G]GTGACTGGCTTGAGT	9921
rs10592227	in-del	-/CT	0.0729998	0.176553	intron-variant	RNF10	GRCh38.p7	12:120546235	TGCAAGAAAAAAACA[-/CT]CTACTATGTGTTGTC	9921
rs10709360	in-del	-/A	0	0	upstream-variant-2KB	RNF10	GRCh38.p7	12:120534014	GAGCGACTCCGCCTC[-/A]AAAAAAAAAAAAAAG	9921
rs10774555	snp	A/G	0.390838	0.206555	upstream-variant-2KB	RNF10	GRCh38.p7	12:120534175	CCCATTATTTTGAAT[A/G]CCCTCACAGTGGGGT	9921
rs10774556	snp	A/G	0.498813	0.0243321	intron-variant	RNF10	GRCh38.p7	12:120557038	AGTCCCAGCTACTCC[A/G]GAGGCTGAGGCAGGA	9921
rs10774557	snp	A/G	0.382279	0.212137	intron-variant	RNF10	GRCh38.p7	12:120560196	CGCTTTTGTTGCCCA[A/G]GCTGGAATGCAGTGG	9921
rs10774558	snp	A/T	0.382666	0.211895	intron-variant	RNF10	GRCh38.p7	12:120571774	CTCTGATTCAGGTGG[A/T]ATTTATCTGTTACAT	9921
rs10849758	snp	C/T	0.389152	0.207694	upstream-variant-2KB	RNF10	GRCh38.p7	12:120533346	AGGTGTGAGCCACCA[C/T]GCCCGGCTGCCCAAC	9921
rs10849759	snp	A/T	0.391024	0.206427	intron-variant	RNF10	GRCh38.p7	12:120556685	AAGTTACTGGTAGAT[A/T]ACTTCTAGACCCTTT	9921
rs10849760	snp	C/T	0.378568	0.214407	intron-variant	RNF10	GRCh38.p7	12:120558865	GTGAGCCACTGTGAC[C/T]GGCCAAGAAAACCAC	9921
rs10849762	snp	A/G	0.382279	0.212137	intron-variant	RNF10	GRCh38.p7	12:120559799	CTCCTGGGTTCAAGC[A/G]ATTTTCTTACTCCAG	9921
rs10849764	snp	C/T	0.382666	0.211895	intron-variant	RNF10	GRCh38.p7	12:120572227	GCCTGCCACCACGCC[C/T]GGCTAATTTTTTGTA	9921
rs11065154	snp	C/T	0.390838	0.206555	upstream-variant-2KB	RNF10	GRCh38.p7	12:120533614	AGTGCCGTAAAGTGA[C/T]ATTAAATGTAAGGTA	9921
rs11065155	snp	A/G	0.244205	0.249933	intron-variant	RNF10	GRCh38.p7	12:120538822	ATGAAGCACTGCCCT[A/G]GCATTCTTCCTGTTA	9921
rs11065156	snp	A/G	0.030665	0.119967	intron-variant	RNF10	GRCh38.p7	12:120544273	CATGCCTTTAATCCT[A/G]ACAGTTTGGAAGGCC	9921
rs11065157	snp	A/G	0.376989	0.215346	intron-variant	RNF10	GRCh38.p7	12:120544897	CAACAATGGGGGATT[A/G]GTTACATTATTCTGT	9921
rs11065158	snp	A/G	0.398354	0.201224	intron-variant	RNF10	GRCh38.p7	12:120544930	gtatgtggccaagaa[A/G]ggtacagcaattaat	9921
rs11065159	snp	A/G	0.0329836	0.124112	intron-variant	RNF10	GRCh38.p7	12:120545778	TCCTGACCTCAGGTG[A/G]TCCACCTGCCTCGGC	9921
rs11065160	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120557097	TCTCAAAAAAAAAAA[A/G]AAAAGAAAAAAATGA	9921
rs11065161	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120562161	CCCACTCTCCACCCT[C/T]TGATAGGCCTCAGTG	9921
rs11065162	snp	G/T	0	0	intron-variant	RNF10	GRCh38.p7	12:120564995	TTATGTATATATTGT[G/T]GGATATCGGGGTTAG	9921
rs11065163	snp	C/T	0.382666	0.211895	intron-variant	RNF10	GRCh38.p7	12:120572434	GTTTGTACTGAGAAA[C/T]AAGCAAGAATTGAGC	9921
rs11272674	in-del	-/TTGGAGAGAATGACATCT			intron-variant	RNF10	GRCh38.p7	12:120543002	TTTAGGTGGTCAGGT[-/TTGGAGAGAATGACATCT]CATTTATACAGTGAG	9921
rs11277370	in-del	-/TCTGTT	0.379354	0.213933	upstream-variant-2KB	RNF10	GRCh38.p7	12:120532965	ATCTGCTTTTTGTTC[-/TCTGTT]TCTACTTTTTAAAAA	9921
rs11373766	in-del	-/A/AA	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120567335	TCGTTTTAATAGCTC[-/A/AA]AAAAAAAAAAAAACA	9921
rs11374622	in-del	-/A	0	0	intron-variant	RNF10	GRCh38.p7	12:120559066	TTAATTTTAAATTAT[-/A]TTTTTTTATTTTAAA	9921
rs11378458	in-del	-/T	0	0	intron-variant	RNF10	GRCh38.p7	12:120570204	TTTTTTTTTTTTTTT[-/T]AAGATGGAGTTTTGC	9921
rs11542860	snp	C/G	0.00398564	0.0444627	utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534530	GCTCGCGCAACCTCC[C/G]TCGCCTCCCCTTCCC	9921
rs11611781	snp	C/T	0.322007	0.239405	intron-variant	RNF10	GRCh38.p7	12:120574653	GTACTTGGCTGGGCA[C/T]GGTGTCTCATGCCTG	9921
rs11611814	snp	A/G	0.136847	0.222927	intron-variant	RNF10	GRCh38.p7	12:120551993	TAGGAGGAAGACTGC[A/G]TAAGAGGAAATGCTA	9921
rs11611938	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120545225	tcgccctgtcaccca[G/T]gctggagtgcagtgg	9921
rs11612519	snp	A/G	0.255503	0.249939	intron-variant	RNF10	GRCh38.p7	12:120576357	TCTCCCAACAACCAC[A/G]TTAAATGGGTGTACC	9921
rs11615264	snp	C/T	0.254944	0.249951	intron-variant	RNF10	GRCh38.p7	12:120551100	aaattatcctcccac[C/T]tcagccttccaagta	9921
rs11830833	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	RNF10	GRCh38.p7	12:120532626	tcttgggctcaagtg[A/G]tcatccctcctcagc	9921
rs12231143	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120567887	tgtgtgtgtgtatgt[A/G]tatatatatatgtaa	9921
rs12304739	snp	A/T	0.0707826	0.174302	intron-variant	RNF10	GRCh38.p7	12:120558579	tatgtatatatatat[A/T]tttttttgagacaga	9921
rs12309824	snp	A/C	0.386313	0.209568	intron-variant	RNF10	GRCh38.p7	12:120552779	TGAGAGGCTTTTTTT[A/C]AGCTATTGTGGGAAA	9921
rs12367471	snp	A/C	0.0103295	0.0711199	upstream-variant-2KB	RNF10	GRCh38.p7	12:120532566	CTTTAAAttttattt[A/C]tttagggacagagtc	9921
rs12369178	snp	C/T	0.398354	0.201224	intron-variant	RNF10	GRCh38.p7	12:120544814	CATAATCACCTAAGC[C/T]TCTgtgtaaagagac	9921
rs12371550	snp	C/T	0.39121	0.2063	intron-variant	RNF10	GRCh38.p7	12:120549840	AAAAAAGGAAGTGGG[C/T]AGTGGACCACAGGAT	9921
rs12814055	snp	A/G	0.391024	0.206427	intron-variant	RNF10	GRCh38.p7	12:120549588	ccaggagtttgagac[A/G]ggcctggctaatgtg	9921
rs12827839	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120552064	actccagcctgggtg[A/T]cagagtgagactctg	9921
rs16950277	snp	A/T	6.61212e-05	0.00574945	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563391	TGAAGAAACCACGGA[A/T]GTTTGTTCTCTGGAC	9921
rs16950279	snp	C/T	0.0752113	0.178743	intron-variant	RNF10	GRCh38.p7	12:120566451	CATGTGTGATGTCCT[C/T]AACTGTTGGAAACTA	9921
rs16950282	snp	A/C	0.0755793	0.179102	intron-variant	RNF10	GRCh38.p7	12:120571525	GAAAAGGAGAGACTT[A/C]ACAGGCTAATGTTGC	9921
rs16950287	snp	A/G	0.0711525	0.174681	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120576264	GGAGAAGTCAGTCTC[A/G]AAGCCTGTTGCACTC	9921
rs16950293	snp	A/G	0.271972	0.249033	downstream-variant-500B	RNF10	GRCh38.p7	12:120577658	CTTGAATAGGTTAAC[A/G]TGACAGCTACTATGA	9921
rs17487343	snp	C/T	0.0372196	0.131242	intron-variant	RNF10	GRCh38.p7	12:120565002	TATATTGTTGGATAT[C/T]GGGGTTAGGACCCCC	9921
rs17487385	snp	A/T	0.0785177	0.181917	intron-variant	RNF10	GRCh38.p7	12:120570553	TAGTAATAAGAGTAC[A/T]GACCATGTGAGGGCC	9921
rs17584461	snp	A/C	0.0785177	0.181917	intron-variant	RNF10	GRCh38.p7	12:120566433	TAGACCTTTGGGGGT[A/C]CGCATGTGTGATGTC	9921
rs17584503	snp	A/G	0.0391387	0.134304	intron-variant	RNF10	GRCh38.p7	12:120570668	CTAGTCAGAATGGAT[A/G]GAGAAGTGTATTACC	9921
rs17852961	snp	G/T	0	0	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120560754	CCAGTACTCCAAGTT[G/T]CTGCTGGCCTCTAAG	9921
rs28437349	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120547081	AAATTGGGAAATAAC[C/T]TAAATGCCTATCTAC	9921
rs28647710	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120535616	ACTTAAAAAACTAAT[A/T]AAAAACAAAACAAAT	9921
rs28874658	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120551628	TATTTTTAAATTTTA[C/G]ATTTTATTTTTTAGA	9921
rs34034209	in-del	-/T	0	0	intron-variant	RNF10	GRCh38.p7	12:120540855	TGCCAGTTTACTTTC[-/T]TTTTTTTTTTTTTTT	9921
rs34120761	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120559176	GGTCTTGAACTACTC[-/T]TTTTTTTTTTTTTTT	9921
rs34126106	in-del	-/T	0.39121	0.2063	downstream-variant-500B	RNF10	GRCh38.p7	12:120577874	TTTCAGTCTCATCCA[-/T]TGTATTATGGAGAAA	9921
rs34167702	in-del	-/A	0.391024	0.206427	intron-variant	RNF10	GRCh38.p7	12:120559157	TCTTGCTATGTTGAT[-/A]GGCTGGTCTTGAACT	9921
rs34289034	in-del	-/C			intron-variant	RNF10	GRCh38.p7	12:120535303	TCATCAGTCCACGCT[-/C]CCTAAAACCACTAAG	9921
rs34444083	in-del	-/TA	0.391024	0.206427	intron-variant	RNF10	GRCh38.p7	12:120558567	ATATAATATAATATG[-/TA]TATATATATATTTTT	9921
rs34649105	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120558168	ATGGTATTGAAACAA[-/T]TTGATTCTCCCTAAG	9921
rs34710944	in-del	-/C			intron-variant	RNF10	GRCh38.p7	12:120548160	AGAACTTCAGTTTGG[-/C]AAATGTTATATGTAC	9921
rs34773021	in-del	-/T/TT	0.472896	0.113214	intron-variant	RNF10	GRCh38.p7	12:120572061	TTTTTTTTTTTTTTT[-/T/TT]CCTCTTCTCCAAGAC	9921
rs34775380	in-del	-/A	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120567701	GCGAGACTTTGTCTC[-/A]AAAAAAAAAAAAAAA	9921
rs34889649	in-del	-/A			intron-variant	RNF10	GRCh38.p7	12:120556531	TGAGACTCCGTCTCA[-/A]AAAAAAAAAAAAAAA	9921
rs34947890	in-del	-/T	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120548660	GATTTTTTTTCTTTC[-/T]TTTTTTTTTTTTTTT	9921
rs34978569	in-del	-/A			intron-variant	RNF10	GRCh38.p7	12:120540319	GGGCATTCATAATTT[-/A]AAAAGTCTGTGCAAG	9921
rs35051578	in-del	-/T	0.337614	0.234145	intron-variant	RNF10	GRCh38.p7	12:120570184	CCACCACACCCAGCC[-/T]TTTTTTTTTTTTTTT	9921
rs35057862	in-del	-/T	0.430136	0.173352	intron-variant	RNF10	GRCh38.p7	12:120553906	AATGACAGTCTTCTG[-/T]TTTTTTTTTTTTTTT	9921
rs35143751	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120554963	GTTCCTGGTTCTTCC[-/T]TGGAGTCCATTTTGT	9921
rs35169785	in-del	-/A	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120544356	AGACCCCAACTCTAC[-/A]AAAAAAAAAAAAAAA	9921
rs35194242	in-del	-/A			intron-variant	RNF10	GRCh38.p7	12:120566762	GTGAGACCCCATCTC[-/A]AAAAAAAAAAAAAAA	9921
rs35217139	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120571732	GGGATACAGCATCAG[-/T]TTTTAACTGGTCTCT	9921
rs35265703	in-del	-/G			intron-variant	RNF10	GRCh38.p7	12:120553446	TTGCTCTGTCACCCA[-/G]GGCTGGAGTGCAGTG	9921
rs35265771	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120569436	GGGATTAGAACCTGG[-/T]TTCTTGAGGACTGCA	9921
rs35271224	in-del	-/T	0.398894	0.200825	intron-variant	RNF10	GRCh38.p7	12:120553251	ACCACCCCCGTCTAA[-/T]TTTTTTATTTTTATT	9921
rs35485584	in-del	-/A			intron-variant	RNF10	GRCh38.p7	12:120575572	GTCAAGGTAGGTCTG[-/A]AAAAGAAGTTGGACC	9921
rs35500973	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120573253	TTTGTCTCAGCGTCC[-/T]TTCATTTTCAACTCA	9921
rs35536836	in-del	-/A/AA			intron-variant	RNF10	GRCh38.p7	12:120567346	CGTTTTAATAGCTCA[-/A/AA]AAAAAAAAAAACAGT	9921
rs35567785	in-del	-/TT			intron-variant	RNF10	GRCh38.p7	12:120572912	TTTTTTTTTTTTTTT[-/TT]AAACTAGGCTTTATT	9921
rs35572445	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120557751	TTGAATATATCTAAG[-/T]CATCAGAAAGTGAAG	9921
rs35590307	in-del	-/T			frameshift-variant, nc-transcript-variant	RNF10	GRCh38.p7	12:120563600	ACGCCTCAGCAGCTC[-/T]TCCTTGTTACTACTT	9921
rs35607217	snp	C/G	0.110872	0.20771	intron-variant	RNF10	GRCh38.p7	12:120550895	GCCACCACACCCGGC[C/G]CAGAATGCGGCGTTA	9921
rs35696148	snp	A/G	0.136847	0.222927	intron-variant	RNF10	GRCh38.p7	12:120545383	ATTTTTAGTAGAGAC[A/G]GGATTTCACTGTGTT	9921
rs35724270	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120559686	CCGTACTCCGCCTGG[G/T]GTTATTTTTTTTTAA	9921
rs35754429	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120535437	CTGGTCCCAGATCCA[-/T]TTCCTCTGTCGAAGA	9921
rs35778168	in-del	-/A			upstream-variant-2KB	RNF10	GRCh38.p7	12:120534004	GAGCGACTCCGCCTC[-/A]AAAAAAAAAAAAAAA	9921
rs35785040	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120554329	ACAAGTGTGAGCCAC[-/T]TGTGCCTGGCCGAGA	9921
rs35926438	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120553141	CAGGCTAGAGTGCGG[G/T]GGCGTGATCTCGGCT	9921
rs35989748	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120564690	CTTCCTTCCCAGTTA[-/T]TTTATTCTGTCAGTG	9921
rs36003775	in-del	-/C			intron-variant	RNF10	GRCh38.p7	12:120546776	CTTGCCTCCTTTTTT[-/C]CCCTGAAGGTTATGA	9921
rs36018229	in-del	-/A	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120557086	AAAAAAAAAAAAAAA[-/A]GAAAAAAATGATCAT	9921
rs36040889	in-del	-/T	0.379746	0.213696	intron-variant	RNF10	GRCh38.p7	12:120545348	ACCATGCCCGGCTAA[-/T]TTTTTTTTTTTTTTT	9921
rs56303470	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120566548	GGGCAGATCACTTGA[G/T]CTCAGGAGTTCAAGA	9921
rs56337100	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120569096	CTGCCTCAGCCTCCA[A/G]GTAGTTTGGATTACA	9921
rs56774004	in-del	-/A	0.466181	0.125563	intron-variant	RNF10	GRCh38.p7	12:120575077	AACCCCGTCTCTACT[-/A]AAAAAAAAAAAATCC	9921
rs57490290	in-del	-/GG/GGTG			intron-variant	RNF10	GRCh38.p7	12:120567861	GCATTTCATTATGGG[-/GG/GGTG]TGTGTGTGTGTGTGT	9921
rs57516040	in-del	-/A/AT/TT			intron-variant	RNF10	GRCh38.p7	12:120558578	TATGTATATATATAT[-/A/AT/TT]TTTTTTTTGAGACAG	9921
rs57531334	in-del	-/GTG	0.109814	0.206997	intron-variant	RNF10	GRCh38.p7	12:120569344	TATTTAAAACTTGTG[-/GTG]ACCATTTTGTTCATA	9921
rs57819919	in-del	-/A			intron-variant	RNF10	GRCh38.p7	12:120566779	AAAAAAAAAAAAAAA[-/A]TTGAATTCTGTAAAT	9921
rs58304342	in-del	-/TTTTTTTTTTTT/TTTTTTTTTTTTTT	0	0	intron-variant	RNF10	GRCh38.p7	12:120569549	CATCTTTTTTTTTTT[-/TTTTTTTTTTTT/TTTTTTTTTTTTTT]GAGACAGGGTCTCGC	9921
rs58440772	snp	C/G	0.0755793	0.179102	intron-variant	RNF10	GRCh38.p7	12:120553324	CAAACTCCTGACCTC[C/G]TGATCCACCTGCCTC	9921
rs58820431	snp	C/T	0.077417	0.180873	intron-variant	RNF10	GRCh38.p7	12:120538441	TTTTCTTGATCTTTC[C/T]GGCTAGAGTCGCATA	9921
rs58940766	snp	G/T	0.0726307	0.176182	intron-variant	RNF10	GRCh38.p7	12:120553684	CTGGGATTACAGGCG[G/T]GAGCCACGGCACCCA	9921
rs59055537	snp	C/T	0.0755793	0.179102	intron-variant	RNF10	GRCh38.p7	12:120538453	TTCCGGCTAGAGTCG[C/T]ATACCACAGTTTCTT	9921
rs59126768	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120545349	CCATGCCCGGCTAAT[-/T]TTTTTTTTTTTTTTT	9921
rs59211409	snp	A/G	0.108402	0.206034	intron-variant	RNF10	GRCh38.p7	12:120566269	CCTTTTTATTATGGA[A/G]ATATCAAGACAAGTA	9921
rs59222685	snp	A/G	0.109461	0.206758	intron-variant	RNF10	GRCh38.p7	12:120574004	TCCCCCAGGGAGGGC[A/G]TTAATCTGTTCATGA	9921
rs59307587	snp	A/G/T	0.0737376	0.17729	intron-variant	RNF10	GRCh38.p7	12:120538993	AGAATTTCAGGGCCC[A/G/T]TTGGCTGGATTCCTT	9921
rs59362568	snp	C/T	0.00318978	0.0398085	intron-variant	RNF10	GRCh38.p7	12:120535533	TGGGTCCCAGTTTGC[C/T]AGACCTTGAGTGAGT	9921
rs59563250	in-del	-/A			intron-variant	RNF10	GRCh38.p7	12:120544373	AAAAAAAAAAAAAAA[-/A]TTGGCTGGGAGTGTT	9921
rs59701890	snp	G/T	0.0341408	0.126114	intron-variant	RNF10	GRCh38.p7	12:120553049	AAAGGTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT	9921
rs60046963	in-del	-/AAG/AGA			downstream-variant-500B	RNF10	GRCh38.p7	12:120578013	TATTCAGGCGCAATA[-/AAG/AGA]AGAGCGGAACTACAA	9921
rs60142817	in-del	-/A/AA	0	0	intron-variant	RNF10	GRCh38.p7	12:120567347	CTCAAAAAAAAAAAA[-/A/AA]CAGTTTAGAAAGCCT	9921
rs60324462	in-del	-/A			intron-variant	RNF10	GRCh38.p7	12:120556557	AAAAAAAAAAAAAAA[-/A]GCTTGAACTCTCACT	9921
rs60839171	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120571703	CTTGTGTACTGGATA[C/T]TATTGTAGGGGCTGG	9921
rs60917018	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120565293	CTGTATCATGAGTCT[C/T]AGTACCTCCTAAACA	9921
rs61125653	in-del	-/A/AAA	0	0	intron-variant	RNF10	GRCh38.p7	12:120556557	AAAAAAAAAAAAAAA[-/A/AAA]GCTTGAACTCTCACT	9921
rs61351912	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120569322	AACAAAGTGTCCATC[A/G]TTGGAATATTTAAAA	9921
rs61509406	in-del	-/T	0	0	intron-variant	RNF10	GRCh38.p7	12:120559177	TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTTGC	9921
rs61534510	snp	G/T	0.0341408	0.126114	intron-variant	RNF10	GRCh38.p7	12:120553057	TTTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT	9921
rs61741840	snp	C/T	6.59457e-05	0.00574182	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120546436	TGGATCCAAGCGTTA[C/T]AATCGCAAACGTGAA	9921
rs61760870	snp	A/G	0.0300927	0.118915	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563043	GATGGCTCCCTTGGC[A/G]AAGGAGTCTGTTTTT	9921
rs61760871	snp	C/T	0.00223886	0.0333829	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120566936	CCGAGGGCCATGGGG[C/T]CCTCTCCATTTCTCC	9921
rs61760872	snp	C/G	0.0405411	0.136482	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575693	TCCAAAGAAAGGTGA[C/G]GATGGTCCACTGGTG	9921
rs61945887	snp	C/T	0.144632	0.226711	intron-variant	RNF10	GRCh38.p7	12:120535929	GTAGGATGTTAGGAG[C/T]TGGCAGAGGCTAGAG	9921
rs61945888	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120539853	AACTTTTTTTTTTCC[C/T]TCAAGACAGTCTTGC	9921
rs61945889	snp	A/T	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120552103	AAAAAAAAAAAAAAT[A/T]CCTCTTCCTGGCCGG	9921
rs61945890	snp	G/T	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120553923	TTTTTTTTTTTTTTG[G/T]TGACAGAGTCTCCCT	9921
rs61945891	snp	C/T	0.0244538	0.107838	intron-variant	RNF10	GRCh38.p7	12:120556283	CTCACGCCTATAATC[C/T]CAGCACTTTGGGAGG	9921
rs61945909	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120570997	TCTTCCTGTACCGGT[C/T]GCTGATTTCACTGGT	9921
rs62783262	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120553039	AAGGAAGAGGAAAGG[G/T]TTTTTTTTTTTTTTT	9921
rs63002361	in-del	-/T/TT	0.375	0.216506	intron-variant	RNF10	GRCh38.p7	12:120551312	TTTTTTTTTTTTTTT[-/T/TT]GAAATGGAGTTTTGC	9921
rs63190362	in-del	-/A	0.497907	0.0322805	intron-variant	RNF10	GRCh38.p7	12:120540079	CCTCATGAGGAACTT[-/A]AAAAAAAAAAAAATA	9921
rs66497230	in-del	-/GTTTCT	0	0	upstream-variant-2KB	RNF10	GRCh38.p7	12:120532968	TGCTTTTTGTTCTCT[-/GTTTCT]ACTTTTTAAAAAAAA	9921
rs66865335	in-del	-/T	0	0	intron-variant	RNF10	GRCh38.p7	12:120540142	TATCTTTTTTTTTTT[-/T]GTAGAGATGGGGGTC	9921
rs71076633	in-del	-/T	0.375	0.216506	intron-variant	RNF10	GRCh38.p7	12:120560155	GTTTTTTTTTTTTTT[-/T]GAGACAGAGTTTCGC	9921
rs71076634	in-del	-/TT	0	0	intron-variant	RNF10	GRCh38.p7	12:120562291	TTTTTTTTTTTTTTT[-/TT]GAGACAGAGTTTTGC	9921
rs71076635	in-del	-/AA	0.46855	0.121392	intron-variant	RNF10	GRCh38.p7	12:120567701	GCGAGACTTTGTCTC[-/AA]AAAAAAAAAAAAAAA	9921
rs71451893	in-del	-/A	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120564606	AAGACCATGTCTCAG[-/A]AAAAAAAAATTGGGC	9921
rs71454649	snp	A/G	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120551765	CTCCTGAGTGGCTGA[A/G]AGTGCAGGTGTGCAT	9921
rs73225245	snp	C/T	0.078151	0.181571	upstream-variant-2KB	RNF10	GRCh38.p7	12:120532830	CCAACCACGCCTAAA[C/T]GAAATTGTTTATCTG	9921
rs73225248	snp	C/G	0.078151	0.181571	upstream-variant-2KB	RNF10	GRCh38.p7	12:120533714	TTAACGCTAGAATAA[C/G]AACCATAAATTGGCC	9921
rs73225249	snp	A/T	0.0391387	0.134304	intron-variant	RNF10	GRCh38.p7	12:120535036	AGAGTCGTTGCTCTC[A/T]TCGGCTGGGTTACTC	9921
rs73225250	snp	A/G	0.00636936	0.0560724	intron-variant	RNF10	GRCh38.p7	12:120538032	CTAACAAAAGGGTAC[A/G]CTCAAGCTCCGCATA	9921
rs73230303	snp	C/T	0.0785177	0.181917	intron-variant	RNF10	GRCh38.p7	12:120542486	AATTGTTACTACTAG[C/T]GCCATGTTTGACACT	9921
rs73230305	snp	C/T	0.0785177	0.181917	intron-variant	RNF10	GRCh38.p7	12:120546972	GCATATATCTATAGT[C/T]TCAAATTTTTTTTAG	9921
rs73230306	snp	A/G	0.0785177	0.181917	intron-variant	RNF10	GRCh38.p7	12:120547533	TCCTGGCCTTAAGCA[A/G]TCCTCTCATCTTGGC	9921
rs73230308	snp	A/G	0.0785177	0.181917	intron-variant	RNF10	GRCh38.p7	12:120549183	GATGGAGGTGGGTTC[A/G]GAGGTAGTTGGAATT	9921
rs73230313	snp	C/T	0.0680775	0.171477	intron-variant	RNF10	GRCh38.p7	12:120557254	CAGTTCTTCAAGCAG[C/T]GAACCTTCTGGTGGC	9921
rs73230314	snp	A/G	0.0785177	0.181917	intron-variant	RNF10	GRCh38.p7	12:120558150	AAGATAGATTTCTCA[A/G]TAAATGGTATTGAAA	9921
rs73230318	snp	C/T	0.0785177	0.181917	intron-variant	RNF10	GRCh38.p7	12:120560134	TTTGAGCTTTTCTTT[C/T]TCTGTGTGTGGTTTT	9921
rs73230322	snp	A/G	0.0785177	0.181917	intron-variant	RNF10	GRCh38.p7	12:120573082	TTTCTGTGTTGAAAA[A/G]AAGTTGCAGATATCC	9921
rs73403975	snp	C/T	0.250168	0.25	intron-variant	RNF10	GRCh38.p7	12:120537347	AAAAACTCATGTAGG[C/T]CGGGTGCGGTGGCTC	9921
rs73403977	snp	A/T	0.0729998	0.176553	intron-variant	RNF10	GRCh38.p7	12:120537640	GTAAAGGCCCTTTGT[A/T]AGATTTTACAAATAA	9921
rs73403991	snp	A/G	0.0729998	0.176553	intron-variant	RNF10	GRCh38.p7	12:120550583	TGTGGAGAATGTGGC[A/G]TTTTTTTGTTTTTTG	9921
rs73403994	snp	C/T	0.0271762	0.113356	intron-variant	RNF10	GRCh38.p7	12:120551973	AACGGGAAGCAGGCA[C/T]ATCTTAGGAGGAAGA	9921
rs74389854	snp	C/G	0	0	intron-variant	RNF10	GRCh38.p7	12:120555732	AATTCCTGACCTCAG[C/G]TGATCCTCCCGACTT	9921
rs74484842	snp	G/T	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120555808	GCCTCTTTTTTTTTT[G/T]GAGACAGTCTTGCTC	9921
rs74574163	snp	C/T	0.0119607	0.0764022	intron-variant	RNF10	GRCh38.p7	12:120575609	TTAAATTCTCTCCCC[C/T]ACTTCTTTCCCACTT	9921
rs74619819	snp	A/G	0.0763149	0.179815	intron-variant	RNF10	GRCh38.p7	12:120573250	CACATTTGTCTCAGC[A/G]TCCTTCATTTTCAAC	9921
rs74733240	snp	C/T	0.0748431	0.178382	upstream-variant-2KB	RNF10	GRCh38.p7	12:120532493	TAGGTAAGAACATCA[C/T]TTGTTAGCTATGTGA	9921
rs74737365	snp	A/G	0.0356815	0.128715	intron-variant	RNF10	GRCh38.p7	12:120536586	GCCGTGTCAGGAAAT[A/G]GCATGTATGCAGACT	9921
rs74743278	snp	A/G			upstream-variant-2KB	RNF10	GRCh38.p7	12:120533398	TATTCTTTAGAGACA[A/G]GGGTCTCGCTATATT	9921
rs74784936	snp	G/T			upstream-variant-2KB	RNF10	GRCh38.p7	12:120533401	TCTTTAGAGACAGGG[G/T]TCTCGCTATATTCCC	9921
rs74797192	snp	A/T	0.5	0	upstream-variant-2KB	RNF10	GRCh38.p7	12:120533150	ACTATGCTTGGCTAA[A/T]TTTTTTTTCTTTCTC	9921
rs74892322	snp	A/T	0.136847	0.222927	upstream-variant-2KB	RNF10	GRCh38.p7	12:120533371	CCCAACTAATTTTTT[A/T]AAAAATATTTTTATT	9921
rs75032459	snp	G/T	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120550616	TGCTTTTTTTTTTTT[G/T]GACGAAGTCTCGCTC	9921
rs75090367	snp	A/C	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120557085	GGAGATGGACCGTCT[A/C]AAAAAAAAAAAAAAA	9921
rs75111771	snp	C/T	0.292266	0.246401	intron-variant	RNF10	GRCh38.p7	12:120572140	GGCGCGATCTTGGCT[C/T]GCTGTAAGCTCCGCC	9921
rs75323518	snp	A/G	0.0123036	0.0774623	intron-variant	RNF10	GRCh38.p7	12:120564022	GCCTAGCCATCCTAA[A/G]TTCACAAACCTTCAA	9921
rs75381630	snp	G/T	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120560153	GTGTGTGGTTTTTTT[G/T]GTTTTTTTTTTTTTT	9921
rs75400502	snp	A/G	0.136847	0.222927	intron-variant	RNF10	GRCh38.p7	12:120542696	TAGCTGGGATTACAG[A/G]CGTGTGGCACCACAC	9921
rs75420991	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120542272	AAGCAATCCTTCCAA[C/G]TCAGCCTCTCAGCTA	9921
rs75499170	snp	A/T	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120575088	TACTAAAAAAAAAAA[A/T]ATCCAAAAATTAGCC	9921
rs75547523	snp	G/T	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120550615	TTGCTTTTTTTTTTT[G/T]GGACGAAGTCTCGCT	9921
rs75652711	snp	C/T	0.0755793	0.179102	intron-variant	RNF10	GRCh38.p7	12:120550246	TAGAACGGAAACCTG[C/T]AGGTGTGGTTGGCTG	9921
rs75668021	snp	A/G	0.0337553	0.125452	intron-variant	RNF10	GRCh38.p7	12:120552985	TCGGCCTTTGACCTT[A/G]AGTAACTTAACAGCT	9921
rs75690030	snp	A/C	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120552083	AGTGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA	9921
rs75731481	snp	C/T	0.0356815	0.128715	intron-variant	RNF10	GRCh38.p7	12:120573060	GTTATATATTTGCTT[C/T]CTCTTTTTTCTGTGT	9921
rs75788994	snp	A/G	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120557104	AAAAAAAAAAAAAGA[A/G]AAAAATGATCATACA	9921
rs75820420	snp	G/T	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120552028	CTTTTTTTTTTTTTT[G/T]AGCTGAGGTCGCGCC	9921
rs75827905	snp	A/G	0.136847	0.222927	intron-variant	RNF10	GRCh38.p7	12:120540686	GAGTTGATTTTGGCA[A/G]CTAAAATCACTAATC	9921
rs75841500	snp	G/T	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120551291	GCGCCCATCCTAGTG[G/T]TTTTTTTTTTTTTTT	9921
rs75894293	snp	C/T			upstream-variant-2KB	RNF10	GRCh38.p7	12:120533362	GCCCGGCTGCCCAAC[C/T]AATTTTTTAAAAAAT	9921
rs75914748	snp	C/G	0.0729998	0.176553	intron-variant	RNF10	GRCh38.p7	12:120551997	AGGAAGACTGCATAA[C/G]AGGAAATGCTACATA	9921
rs75928248	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120556347	AGACCATCCTGGCTA[A/C]CACGGTGAAACCCCG	9921
rs75983791	snp	G/T	0.00517822	0.0506191	intron-variant	RNF10	GRCh38.p7	12:120556231	TATGAGCAGGGGCTT[G/T]TGACCTTAAAGCTTG	9921
rs76073173	snp	A/G	0.0752113	0.178743	intron-variant	RNF10	GRCh38.p7	12:120556865	GCTTAAAGAGCTATC[A/G]TACAAAGCCAGGCGC	9921
rs76181214	snp	C/T	0.101319	0.200983	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575982	GAGTGCCCAGGGTTG[C/T]CAAACATACTACACA	9921
rs76183013	snp	C/G	0.0360663	0.129354	intron-variant	RNF10	GRCh38.p7	12:120564153	AGTTAATGCTGTTCC[C/G]TGCTTCTCTGGTTCA	9921
rs76237390	snp	G/T	0.0337553	0.125452	intron-variant	RNF10	GRCh38.p7	12:120549855	CAGTGGACCACAGGA[G/T]CTAAGCCAAATCTGA	9921
rs76260752	snp	A/T	0.0748431	0.178382	upstream-variant-2KB	RNF10	GRCh38.p7	12:120532775	GAGCTTCAGCACAGT[A/T]GACCAAACCAAAACA	9921
rs76349174	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120542273	AGCAATCCTTCCAAC[A/T]CAGCCTCTCAGCTAG	9921
rs76563683	snp	C/T	0	0	intron-variant	RNF10	GRCh38.p7	12:120537682	CTTGAGGCAGCATTC[C/T]TTTTTTTTTGTTTAA	9921
rs76584805	snp	G/T	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120540869	CTTTTTTTTTTTTTT[G/T]TTGAGACAGAGTTTT	9921
rs76699329	snp	A/G	0.322245	0.239334	intron-variant	RNF10	GRCh38.p7	12:120557081	CCAAGGAGATGGACC[A/G]TCTCAAAAAAAAAAA	9921
rs76740462	snp	A/C/G/T	0.0218838	0.102303	intron-variant	RNF10	GRCh38.p7	12:120576570	TTTAAGTTAAGCTGT[A/C/G/T]TTTCTGTGTCTCCCT	9921
rs77292633	snp	A/G	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120536263	CCTCGTCTCCATAAG[A/G]AAAAAAAAAAATTAG	9921
rs77368762	snp	C/T	0.0399052	0.1355	intron-variant	RNF10	GRCh38.p7	12:120572491	GGAACATGAAATAAT[C/T]GTGGAGGTGAGGTGA	9921
rs77374590	snp	A/G/T	0.0252424	0.109538	intron-variant	RNF10	GRCh38.p7	12:120546267	TTGCTCAAAGCACTC[A/G/T]TGCTCTGGCCCAAAC	9921
rs77387369	snp	A/T	0.0755793	0.179102	intron-variant	RNF10	GRCh38.p7	12:120550462	CTAAGTTTGGGGCAT[A/T]AAGGGTGGAAGACCG	9921
rs77405287	snp	A/C	0	0	intron-variant	RNF10	GRCh38.p7	12:120567702	CGAGACTTTGTCTCA[A/C]AAAAAAAAAAAAAAA	9921
rs77621371	in-del	-/AA			intron-variant	RNF10	GRCh38.p7	12:120557108	AAAAAAAAAGAAAAA[-/AA]TGATCATACATGTAC	9921
rs77627710	snp	A/C	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120568243	CAGCCAGACCCTCTC[A/C]AAAAAAAAAAGAAAA	9921
rs77682502	snp	A/G	0.00993419	0.0697739	intron-variant	RNF10	GRCh38.p7	12:120541133	AAGCATTGGGATTAT[A/G]GGCATGAGCCACCGT	9921
rs77866404	snp	C/G			upstream-variant-2KB	RNF10	GRCh38.p7	12:120533400	TTCTTTAGAGACAGG[C/G]GTCTCGCTATATTCC	9921
rs77933939	snp	A/C/G	0.00245903	0.0349781	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120560735	TTATAGATGAACAGC[A/C/G]CAGCCAGTACTCCAA	9921
rs77955762	snp	C/T	0.292266	0.246401	intron-variant	RNF10	GRCh38.p7	12:120572145	GATCTTGGCTTGCTG[C/T]AAGCTCCGCCTCCCG	9921
rs77959261	snp	A/T	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120555655	ACCACTCCCAGCTAA[A/T]TTTTTTTTGTATTTT	9921
rs77992287	snp	A/G	0.0356815	0.128715	intron-variant	RNF10	GRCh38.p7	12:120535448	ATCCATTCCTCTGTC[A/G]AAGAGGAAGTCATCC	9921
rs78091129	snp	A/T	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120555653	CCACCACTCCCAGCT[A/T]ATTTTTTTTTGTATT	9921
rs78198329	snp	A/C	0.5	0	upstream-variant-2KB	RNF10	GRCh38.p7	12:120534004	AGAGCGACTCCGCCT[A/C]AAAAAAAAAAAAAAA	9921
rs78225964	snp	A/C	0.5	0	upstream-variant-2KB	RNF10	GRCh38.p7	12:120534005	GAGCGACTCCGCCTC[A/C]AAAAAAAAAAAAAAG	9921
rs78299441	snp	C/T	0.0759472	0.179459	intron-variant	RNF10	GRCh38.p7	12:120573113	TGAATGATACTTTAC[C/T]GCTAAGTACTTAGGA	9921
rs78445606	snp	A/C	0	0	intron-variant	RNF10	GRCh38.p7	12:120544357	AGACCCCAACTCTAC[A/C]AAAAAAAAAAAAAAA	9921
rs78640946	snp	C/T	0.00557542	0.0525036	intron-variant	RNF10	GRCh38.p7	12:120540474	CTCCTGTTCTACCCT[C/T]GAGTTTTTCCCATGT	9921
rs78656582	snp	C/T	0.00597247	0.0543191	intron-variant	RNF10	GRCh38.p7	12:120550428	GAGGATTTTGTTGAC[C/T]GAGCACAAGCTCTTA	9921
rs78714477	snp	G/T	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120550617	GCTTTTTTTTTTTTG[G/T]ACGAAGTCTCGCTCT	9921
rs78714658	snp	A/G	0.292266	0.246401	intron-variant	RNF10	GRCh38.p7	12:120572141	GCGCGATCTTGGCTT[A/G]CTGTAAGCTCCGCCT	9921
rs78733951	snp	A/C	0.137187	0.223099	intron-variant	RNF10	GRCh38.p7	12:120546829	ATTTCCTTTATGACA[A/C]ATTTGGGGTTCCTTA	9921
rs78750822	snp	A/C	0.0509478	0.151255	intron-variant	RNF10	GRCh38.p7	12:120537944	GCCTTAGGAACGTAA[A/C]AGCTAAGACCAGTGC	9921
rs78780669	snp	C/T	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120537681	CCTTGAGGCAGCATT[C/T]TTTTTTTTTTGTTTA	9921
rs78853682	snp	G/T	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120560166	TTTGTTTTTTTTTTT[G/T]TTGAGACAGAGTTTC	9921
rs78983640	snp	G/T	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120560154	TGTGTGGTTTTTTTT[G/T]TTTTTTTTTTTTTTG	9921
rs79079641	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120566004	TTTGATCTGGTTCTC[A/C]AAAATAAGTTTCATT	9921
rs79185082	snp	G/T	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120560169	GTTTTTTTTTTTTTT[G/T]AGACAGAGTTTCGCT	9921
rs79185674	snp	G/T	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120551309	TTTTTTTTTTTTTTT[G/T]TTTGAAATGGAGTTT	9921
rs79207443	snp	C/T	0.0391733	0.134358	intron-variant	RNF10	GRCh38.p7	12:120560925	TAAACCTTTTCACTT[C/T]CTCGGCGTTCTGTGG	9921
rs79245244	snp	C/G	0.0154538	0.0865337	intron-variant	RNF10	GRCh38.p7	12:120548407	AGAAGAGAGCACAGT[C/G]AGGGCGGGAGGAAAA	9921
rs79287466	snp	A/C	0.5	0	upstream-variant-2KB	RNF10	GRCh38.p7	12:120534006	AGCGACTCCGCCTCA[A/C]AAAAAAAAAAAAAGA	9921
rs79428211	snp	A/C	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120557087	AGATGGACCGTCTCA[A/C]AAAAAAAAAAAAAAG	9921
rs79563051	snp	G/T	0	0	upstream-variant-2KB	RNF10	GRCh38.p7	12:120532350	GTGGGTGGATCACGA[G/T]GTCAGGAGTTCGAGA	9921
rs79661429	snp	A/C	0	0	intron-variant	RNF10	GRCh38.p7	12:120544356	GAGACCCCAACTCTA[A/C]AAAAAAAAAAAAAAA	9921
rs79704806	snp	C/T	0.0755793	0.179102	intron-variant	RNF10	GRCh38.p7	12:120573567	GTATAAAAGATTACC[C/T]GACGCCGAGTCATTT	9921
rs79736037	snp	C/T	0.0752113	0.178743	upstream-variant-2KB	RNF10	GRCh38.p7	12:120534307	ACATTTCCCAGAATA[C/T]CTCACCCCCTCTCCA	9921
rs79890883	snp	A/T	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120552101	AAAAAAAAAAAAAAA[A/T]TTCCTCTTCCTGGCC	9921
rs79920634	in-del	-/AAAAAA			intron-variant	RNF10	GRCh38.p7	12:120540087	GGAACTTAAAAAAAA[-/AAAAAA]TAGGGGTGTGTGGGG	9921
rs80072520	snp	C/T	0.0154538	0.0865337	intron-variant	RNF10	GRCh38.p7	12:120565329	TCTGTTCATCTAGTC[C/T]AGCTGGGCCTACTGT	9921
rs80103950	in-del	-/TTTTTT			intron-variant	RNF10	GRCh38.p7	12:120572916	TTTTTTTTTTTTTTT[-/TTTTTT]AAACTAGGCTTTATT	9921
rs80136474	snp	G/T	0.0244538	0.107838	intron-variant	RNF10	GRCh38.p7	12:120550543	TGGAAGTCTTGGGCT[G/T]CCTGTGTTGCACAAG	9921
rs80201714	snp	C/G	0.0741063	0.177655	intron-variant	RNF10	GRCh38.p7	12:120561553	CTTAGAGCAATAGAA[C/G]CCCATATTTATTGAG	9921
rs111247951	in-del	-/T	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120552014	GGAAATGCTACATAC[-/T]TTTTTTTTTTTTTGA	9921
rs111294792	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120550765	CCATGCCCAGCTAAT[A/T]TTTTGTATTTTTAGT	9921
rs111406025	snp	A/G	0	0	intron-variant	RNF10	GRCh38.p7	12:120555635	TGGGACTACAGGCAC[A/G]CACCACCACTCCCAG	9921
rs111468271	snp	C/T	0.0729998	0.176553	intron-variant	RNF10	GRCh38.p7	12:120552215	GCATGGTCAACATGG[C/T]GAAACCCTGTCTCTA	9921
rs111482782	snp	A/T	0.0399286	0.135536	intron-variant	RNF10	GRCh38.p7	12:120570019	TGCCCCAGCCTCCTG[A/T]GTAGCTGTGTAGCGT	9921
rs111483466	snp	A/G/T	9.89001e-05	0.00703151	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546441	CCAAGCGTTATAATC[A/G/T]CAAACGTGAACTTTC	9921
rs111484991	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120545775	AACTCCTGACCTCAG[A/G]TGATCCACCTGCCTC	9921
rs111919381	snp	C/T	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120539993	GTGTCCACCACCACA[C/T]CGGCCTAATTTTTGT	9921
rs112105384	snp	A/G	0.0752113	0.178743	intron-variant	RNF10	GRCh38.p7	12:120567631	GCTTGAACCTGGGAG[A/G]CGGAGGTCTCAGTGA	9921
rs112124375	snp	C/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120548344	TGAGTGTTCCAAAAA[C/T]GGATTAGGTTCAAGA	9921
rs112380143	snp	G/T	0.0810805	0.184299	intron-variant	RNF10	GRCh38.p7	12:120539801	TAGTTCTTGGCAGTT[G/T]TTCTCAGTGGTGGCT	9921
rs112461916	snp	C/T	0.0322114	0.122752	downstream-variant-500B	RNF10	GRCh38.p7	12:120577851	TTTCTGTTAAATGTG[C/T]ATGGTACTTTCAGTC	9921
rs112635551	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120549396	GTTGTATTTGTTAGC[C/T]CTGTTTGTCTGCTGC	9921
rs112642341	snp	A/G	0.0755793	0.179102	intron-variant	RNF10	GRCh38.p7	12:120540350	TGATTCTGGTGTGCA[A/G]CCAGGATTGAGAACC	9921
rs112757664	in-del	-/A	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120552400	GTAAGACTCCGTCTC[-/A]AAAAAAAAAGCTGTG	9921
rs112784456	snp	A/C	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120574897	GCGCCATTGCACTCC[A/C]GCCTGGGCAACAAGA	9921
rs112788889	snp	A/C	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120564609	ACCATGTCTCAGAAA[A/C]AAAAAATTGGGCTTC	9921
rs112865272	snp	A/C	0.118584	0.212673	intron-variant	RNF10	GRCh38.p7	12:120541965	CCCGCCTCCCAGGTT[A/C]ACACCGTTCTCCTGC	9921
rs113009191	snp	A/G	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120556142	GAAGTTATAAACTCT[A/G]GGTATCCCCTTGTTG	9921
rs113121287	snp	C/G			splice-donor-variant	RNF10	GRCh38.p7	12:120552699	CTTTTTACAGGCCAA[C/G]TGAGTATTGCTACCC	9921
rs113139244	snp	C/G	0.000349142	0.0132079	utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534783	CGCCCGCTCCGCTCC[C/G]ACTGCCGTCGCCGCC	9921
rs113273581	snp	G/T	0.5	0	upstream-variant-2KB	RNF10	GRCh38.p7	12:120532992	TTTTAAAAAAAAGTT[G/T]AGACAGGGTCTCCCT	9921
rs113281996	snp	C/T	0.0123036	0.0774623	intron-variant	RNF10	GRCh38.p7	12:120547762	AGGGATCAGATCATG[C/T]GGGGCTTTGAAGGAC	9921
rs113282879	snp	G/T	0	0	downstream-variant-500B	RNF10	GRCh38.p7	12:120578012	TGTATTCAGGCGCAA[G/T]AAGAGCGGAACTACA	9921
rs113308343	snp	A/G	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120549507	GTGGGTGATGGGGCC[A/G]GGCGCAGTGGCTCAC	9921
rs113311592	snp	C/T	0	0	intron-variant	RNF10	GRCh38.p7	12:120567286	TACTCCCCTGTATGC[C/T]TAAACATCTTTGTAC	9921
rs113333301	in-del	-/A	0.5	0	intron-variant	RNF10	GRCh38.p7	12:120573585	GCCGAGTCATTTATC[-/A]AAAAAAAAAAAAAAA	9921
rs113372731	snp	A/G	0.00835141	0.0640778	intron-variant	RNF10	GRCh38.p7	12:120555702	GGTTTCTCCATGTTG[A/G]TCAGGCTGGTCTTGA	9921
rs113425941	snp	A/G	0.0126979	0.078662	intron-variant	RNF10	GRCh38.p7	12:120554608	TGCCTCATGAACCAG[A/G]GCTGCTAATGGCCTG	9921
rs113454376	snp	C/G	0.0755793	0.179102	intron-variant	RNF10	GRCh38.p7	12:120536372	TGAGGCTGCGGTGAG[C/G]TATATCACGATACTG	9921
rs113508474	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120572513	GTGAGGTGAGAAGAG[A/G]GGGGGATCCTGAAAA	9921
rs113560686	snp	C/G			missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120566879	TTCCTGCCTTCAATT[C/G]TTATACCTGCTCCTC	9921
rs113602432	snp	C/T	0.136847	0.222927	intron-variant	RNF10	GRCh38.p7	12:120569554	TTTTTTTTTTTGAGA[C/T]AGGGTCTCGCTCTGT	9921
rs113611687	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120566102	CCCAGAAAAGGACTT[C/T]GGTGTTTTGACTCCA	9921
rs113724341	snp	C/T	0.108755	0.206276	intron-variant	RNF10	GRCh38.p7	12:120568695	TGGCCAGGCTGGTCT[C/T]GAACTCCTGGCCTCA	9921
rs113747194	snp	A/G	0.0729998	0.176553	intron-variant	RNF10	GRCh38.p7	12:120541085	TGGTCTCGAACTCCC[A/G]ACCTCAGGTGATCCG	9921
rs113759866	snp	A/G	0.0788843	0.182262	intron-variant	RNF10	GRCh38.p7	12:120555582	AACCTCTGCCTGCCA[A/G]GTTCAAGCGATTCTC	9921
rs113763821	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120556816	GTATTAGTTTTATTA[C/T]ATTTAACGGTTATTA	9921
rs113889003	snp	C/T	0.0729998	0.176553	intron-variant	RNF10	GRCh38.p7	12:120543581	CTGAGGCTGGTGGAT[C/T]GCTTGAGCTCAGGAG	9921
rs113900199	in-del	-/AGA/GAA	0	0	downstream-variant-500B	RNF10	GRCh38.p7	12:120578014	ATTCAGGCGCAATAA[-/AGA/GAA]GAGCGGAACTACAAA	9921
rs113973960	snp	G/T	0.272241	0.249009	intron-variant	RNF10	GRCh38.p7	12:120543957	AACATGCTGGGCATG[G/T]TGGCTCATGCCTGTA	9921
rs114065753	snp	G/T	0.0225045	0.103662	intron-variant	RNF10	GRCh38.p7	12:120560096	CCATTTCTTTATTCT[G/T]TATTGTTGGTTTTAC	9921
rs114112489	snp	A/G	0.0111196	0.0737302	intron-variant	RNF10	GRCh38.p7	12:120569693	ACAGGCAGCACCACC[A/G]TACCCTGCTAATTTT	9921
rs114353985	snp	C/T	0.0337553	0.125452	intron-variant	RNF10	GRCh38.p7	12:120551073	CCACTGCAGCCTTGA[C/T]CTACTGGGCTCAAAT	9921
rs114414203	snp	A/C/G	0.00478085	0.0486577	intron-variant	RNF10	GRCh38.p7	12:120566020	AAAATAAGTTTCATT[A/C/G]AATCCAGGGGATTAG	9921
rs114646723	snp	A/G	0.0170251	0.090679	intron-variant	RNF10	GRCh38.p7	12:120571793	TATCTGTTACATAAA[A/G]TGAGCCATTTCTCTT	9921
rs114775205	snp	C/T	0.000692372	0.0185932	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546537	TTAACAAGATGCCTC[C/T]TCAAAGGGGCGGCGG	9921
rs114823195	snp	A/G	0.0248432	0.108648	intron-variant	RNF10	GRCh38.p7	12:120549229	TAATTTTCTCAGTGG[A/G]ATATCTAAGGTGAGC	9921
rs114853199	snp	G/T	0.0244538	0.107838	intron-variant	RNF10	GRCh38.p7	12:120539627	CTTAATTTGGTAATG[G/T]GGGGAGGCTGAGATA	9921
rs114971948	snp	G/T	0.0197687	0.0974348	intron-variant	RNF10	GRCh38.p7	12:120569856	CTGTGATACCGAGAT[G/T]GTGTTTTCACATACT	9921
rs115181663	snp	A/G	0.0345262	0.126772	intron-variant	RNF10	GRCh38.p7	12:120567658	GTGAGACAAGGTTGC[A/G]TCACTGCATTCCAGC	9921
rs115557041	snp	A/G	0.00358779	0.0422022	intron-variant	RNF10	GRCh38.p7	12:120539543	TCTGACCTCTAGGCC[A/G]AGCCACCTGTTAGAA	9921
rs115569479	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120548660	GGATTTTTTTTCTTT[C/T]TTTTTTTTTTTTTTT	9921
rs116178325	snp	A/G	0.0126979	0.078662	intron-variant	RNF10	GRCh38.p7	12:120547031	CATAAAGACATTTAT[A/G]TACAAGGGTATTCAC	9921
rs116264015	snp	C/T	0.00358779	0.0422022	intron-variant	RNF10	GRCh38.p7	12:120572122	CCCAGGCTGGAGTTC[C/T]GTGGCGCGATCTTGG	9921
rs116409253	snp	G/T	0.0126979	0.078662	intron-variant	RNF10	GRCh38.p7	12:120546979	TCTATAGTCTCAAAT[G/T]TTTTTTAGGAGTTTC	9921
rs116412176	snp	C/T	0.0158469	0.0875917	intron-variant	RNF10	GRCh38.p7	12:120550323	GAGTTCAGGGTATTG[C/T]GAGGATAATCAGGAA	9921
rs116491325	snp	A/G	0.0162398	0.0886349	intron-variant	RNF10	GRCh38.p7	12:120566052	GTGACCTGAGGTCCC[A/G]TTATCCACTAGAACA	9921
rs116505392	snp	A/G	0.00318978	0.0398085	intron-variant	RNF10	GRCh38.p7	12:120566092	GAGTCCTTGGCCCAG[A/G]AAAGGACTTCGGTGT	9921
rs116720495	snp	A/G	0.0185938	0.0946107	intron-variant	RNF10	GRCh38.p7	12:120546068	TCCTTAATACAGAAT[A/G]CCTGTTTCATTTCCT	9921
rs116727495	snp	A/G	0.00365034	0.0425658	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120562975	CTGTCGGGATTGGCC[A/G]GAAGCAGAAGGGAGG	9921
rs116987251	snp	A/G	0.0437281	0.141251	intron-variant	RNF10	GRCh38.p7	12:120572289	GCCAGTAGGGTCTCA[A/G]TCTCCTGACCTCGTG	9921
rs117054838	snp	C/G	0.0785177	0.181917	intron-variant	RNF10	GRCh38.p7	12:120555797	CATCGTACCTGGCCT[C/G]TTTTTTTTTTTGAGA	9921
rs117112459	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120555118	CATTGGCAGCCATTC[A/G]TAGCAATCACTATCA	9921
rs117264981	snp	A/C	0.0785177	0.181917	intron-variant	RNF10	GRCh38.p7	12:120559822	TACTCCAGCCTCCCT[A/C]GTAGCTGGGATTATA	9921
rs117311262	snp	C/T	0.00358779	0.0422022	upstream-variant-2KB	RNF10	GRCh38.p7	12:120533729	GAACCATAAATTGGC[C/T]GGGCGCGGTGGCTCA	9921
rs117319218	snp	G/T	0.00755907	0.0610114	intron-variant	RNF10	GRCh38.p7	12:120535191	TGCTCGATTAAGCAG[G/T]TGCTGTTCTTATCGC	9921
rs117382618	snp	A/G	0.00318978	0.0398085	intron-variant	RNF10	GRCh38.p7	12:120561624	TCACTTAAGCTTCTA[A/G]TGTGGTAGATAGAAC	9921
rs117533586	snp	A/G	0.00993419	0.0697739	intron-variant	RNF10	GRCh38.p7	12:120544958	AATCATGCTTCTGAA[A/G]ACTAGGGATGCATAA	9921
rs117584449	snp	C/T	0.029116	0.117091	intron-variant	RNF10	GRCh38.p7	12:120555988	GAGACGGGGTTCCAC[C/T]GTGTTGTCCAGGCTT	9921
rs117725109	snp	C/T	0.0785177	0.181917	intron-variant	RNF10	GRCh38.p7	12:120543748	GAGGCTGCAGTAAGC[C/T]GAGATCATGCCACTG	9921
rs117747152	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120562068	GTAAACCTGTGTCAT[A/G]GGGGTTTGTTATACA	9921
rs118143694	snp	C/T	0.0256215	0.110247	intron-variant	RNF10	GRCh38.p7	12:120548891	TAGCCACGGTGGTCT[C/T]GATCTTCTGACCTTG	9921
rs118152539	snp	G/T	0.0232847	0.105357	intron-variant	RNF10	GRCh38.p7	12:120544568	AGGCTGAAGTGGGAG[G/T]GTGGCTTGAGCCTGA	9921
rs118185033	snp	C/T	0.0123036	0.0774623	intron-variant	RNF10	GRCh38.p7	12:120556910	GTAATTCCAGGACTT[C/T]GGGAGGCCGAGGCGG	9921
rs137862286	snp	C/G	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120537181	CGTGGTGGCACGCAC[C/G]TGTAGTCCCAGCTGT	9921
rs137902657	snp	A/G	0.000115513	0.00759888	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546548	CCTCCTCAAAGGGGC[A/G]GCGGCAGCAGCAAAC	9921
rs137927490	snp	A/G	0.00478085	0.0486577	intron-variant	RNF10	GRCh38.p7	12:120565800	GGGAATTGGGGCTTC[A/G]CTAAGAATGCTGGGG	9921
rs137974756	snp	G/T	0.0785177	0.181917	intron-variant	RNF10	GRCh38.p7	12:120559552	ACCACACCTGGCTAG[G/T]TTTTGTATTTTTAGT	9921
rs138031591	snp	C/G	1.74821e-05	0.00295647	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563600	CACGCCTCAGCAGCT[C/G]TCCTTGTTACTACTT	9921
rs138042413	snp	C/G	0.00438332	0.0466095	intron-variant	RNF10	GRCh38.p7	12:120559938	CTAACTTCAGGTGAT[C/G]CACCTGCCTCAGCCT	9921
rs138042726	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120568897	AGAGTGCTGGGATTC[C/T]AGGTGTGAGCCACTG	9921
rs138120728	snp	C/T	0.0189856	0.0955633	intron-variant	RNF10	GRCh38.p7	12:120536088	TTTGAAGTCCCTAAA[C/T]GTGGAGGTCCAGTTT	9921
rs138164075	snp	A/G	0.0263992	0.111815	intron-variant	RNF10	GRCh38.p7	12:120556069	GTTGGGATTACAGGC[A/G]TGAGCCACCACGCCC	9921
rs138268654	in-del	-/A			intron-variant	RNF10	GRCh38.p7	12:120565869	CTCTGACTCTTTATT[-/A]AAGGGACCAGCTATA	9921
rs138359658	snp	A/G	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120569297	TGCCTGGCCTCTGTC[A/G]GGCATTCTTAACAAA	9921
rs138470008	snp	A/G	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120549511	GTGATGGGGCCGGGC[A/G]CAGTGGCTCACAGCT	9921
rs138491572	snp	C/T	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120542234	GGTGCCATCATAGCA[C/T]ACCGCAGCCTCAACC	9921
rs138683853	snp	C/G/T	3.29838e-05	0.00406092	missense, synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563499	AGAGGCCTGTGATGA[C/G/T]TTGGAGTTAGCAGAT	9921
rs138738342	snp	A/G/T	9.97407e-05	0.00706119	synonymous-codon, missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120565465	TCAGCGCCAAAAGAA[A/G/T]GCTCGGGAGGAACGC	9921
rs138783662	snp	C/T	0.00478085	0.0486577	intron-variant	RNF10	GRCh38.p7	12:120564710	TTCTGTCAGTGGTTC[C/T]CAGGTTTTTTTCTGT	9921
rs138808962	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120559840	AGCTGGGATTATAGG[C/T]GCCCGTCACCACGCC	9921
rs138848226	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120568661	TTGTATTTTTAATAG[A/C]GACAGGGTCTCTCCA	9921
rs139020183	snp	C/T	0.078151	0.181571	intron-variant	RNF10	GRCh38.p7	12:120545282	GCCTCCTGGGGTTCA[C/T]GCCGTTCTCCTGCCT	9921
rs139040272	snp	C/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120573023	CTTTTGACCTAGATT[C/T]ACTAATTGTTACTAT	9921
rs139119394	snp	C/T	0.00517822	0.0506191	intron-variant	RNF10	GRCh38.p7	12:120554600	TAGTGCAGTGCCTCA[C/T]GAACCAGGGCTGCTA	9921
rs139168584	snp	A/G	0.0178098	0.0926698	intron-variant	RNF10	GRCh38.p7	12:120554035	TTAGCCTCCTAAGTA[A/G]CTGGGACTACAGGCG	9921
rs139223862	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120550949	AAAAAAGGAAGTTAT[C/T]TGACTGGATGGTATA	9921
rs139229598	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120540664	AGGTAACTGGAAGAC[A/G]AGAAACGAGTTGATT	9921
rs139332694	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120573946	CAGTGGCAGACATCA[C/G]TCATCAGCTCTTTCA	9921
rs139390378	in-del	-/AAG	0.379942	0.213577	downstream-variant-500B	RNF10	GRCh38.p7	12:120578012	GTATTCAGGCGCAAT[-/AAG]AAGAGCGGAACTACA	9921
rs139403078	snp	A/C/T	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120561502	ATTCTGATGGCTGCT[A/C/T]ATCCCCAGACCACAC	9921
rs139403251	snp	C/G	9.98901e-05	0.00706648	intron-variant	RNF10	GRCh38.p7	12:120560687	ACCATCGTGAGCTTT[C/G]AATGTTGCATTTCTT	9921
rs139558500	snp	C/T	3.29527e-05	0.00405898	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120566886	CTTCAATTCTTATAC[C/T]TGCTCCTCTGATTCT	9921
rs139592862	in-del	-/A	0.0785177	0.181917	intron-variant	RNF10	GRCh38.p7	12:120551538	TCCTGACCTCAGGTG[-/A]TCCGCCTACCTCAGC	9921
rs139601055	snp	C/T	0.000247066	0.0111118	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120562974	TCTGTCGGGATTGGC[C/T]GGAAGCAGAAGGGAG	9921
rs139676525	snp	C/T	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120570966	CTAGAGTTACTGTAA[C/T]GATGAAGCTCTTCCC	9921
rs139711502	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120537732	GACCATGTTTGCCAC[C/T]GCCAGTGTCTGCTTT	9921
rs139788197	snp	A/G	1.64803e-05	0.00287052	synonymous-codon, missense, nc-transcript-variant, intron-variant	RNF10	GRCh38.p7	12:120571198	CCTTTCAGACTTTCT[A/G]CTGACCCCTCTGTCA	9921
rs139810953	snp	G/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120574963	GAGGGTACTAGGCCG[G/T]GCACAGTGGCTCACG	9921
rs139895552	snp	A/G/T	0.0178098	0.0926698	intron-variant	RNF10	GRCh38.p7	12:120552273	GGTTTAATCCCACAC[A/G/T]CCTGTAATCCCAGCT	9921
rs139927970	snp	G/T	0.00914312	0.0669923	intron-variant	RNF10	GRCh38.p7	12:120554416	AGAGGAAATCTGGCT[G/T]ACTGCTGTTTGATGG	9921
rs139972463	snp	A/G	3.29734e-05	0.00406025	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120560838	GCTGGCAGAGGAGAA[A/G]CACACTCCCGAGTCC	9921
rs140008777	snp	C/G	0.00398564	0.0444627	intron-variant	RNF10	GRCh38.p7	12:120546200	TGTTTTGAGGGAGGG[C/G]ACCCGTTAGGCTTCA	9921
rs140042315	in-del	-/CCT	0.0752113	0.178743	cds-indel, nc-transcript-variant	RNF10	GRCh38.p7	12:120534593	ACTCCCGAGCCCCGG[-/CCT]CCTCGTCCTCGGTCG	9921
rs140165853	snp	C/T	0.000757501	0.0194468	synonymous-codon, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575826	TCCTGCCCCTGTGGA[C/T]AGCGACGGGGAGAGT	9921
rs140267477	snp	C/T	0.00557542	0.0525036	intron-variant	RNF10	GRCh38.p7	12:120544595	CTGAGAGGTGGAGGT[C/T]GTAGTGAACGAGATT	9921
rs140501925	snp	C/T	0.0337553	0.125452	intron-variant	RNF10	GRCh38.p7	12:120555836	CTCTGTCGCCCCAGC[C/T]GGAGTGCAGTGGCGC	9921
rs140592884	snp	A/G	0.0189856	0.0955633	intron-variant	RNF10	GRCh38.p7	12:120567429	ACCAGAAGGCCGGGC[A/G]TGGTGGCTTATGCCT	9921
rs140614674	snp	A/G	4.94458e-05	0.00497197	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546447	GTTATAATCGCAAAC[A/G]TGAACTTTCCTACCC	9921
rs140658625	snp	A/G	0.00279162	0.0372561	intron-variant	RNF10	GRCh38.p7	12:120544182	CAGTGAGCCGAGATT[A/G]CGCCACTGCACTCCA	9921
rs140664614	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120547702	AGCAAGTAGGCTACC[A/G]TAAGTGGAGGAGGAG	9921
rs140812598	in-del	-/TA			intron-variant	RNF10	GRCh38.p7	12:120558568	TATAATATAATATGT[-/TA]ATATATATATTTTTT	9921
rs140878921	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120545023	ATCTTCTATGCTTGT[C/T]ATTTTATATAAGATT	9921
rs140944218	snp	A/G	0.0023933	0.0345097	intron-variant	RNF10	GRCh38.p7	12:120548345	GAGTGTTCCAAAAAC[A/G]GATTAGGTTCAAGAA	9921
rs140980445	snp	A/G	0.0189856	0.0955633	upstream-variant-2KB	RNF10	GRCh38.p7	12:120533932	GAATGGCGTGAACCC[A/G]GGAGGCGGAGCTTGC	9921
rs141133066	snp	C/G/T	0.00358779	0.0422022	intron-variant	RNF10	GRCh38.p7	12:120572688	GCAACCACCGCCTCC[C/G/T]GGGTTCAAGCAATTC	9921
rs141191211	snp	C/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120536992	TTAACTCTGATTACC[C/T]AACAAGATGATACAG	9921
rs141295691	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120568686	TCTCCATGTTGGCCA[C/G]GCTGGTCTCGAACTC	9921
rs141319399	snp	C/T	0.00318978	0.0398085	intron-variant	RNF10	GRCh38.p7	12:120561942	ACTAGGTTAGTTTCA[C/T]GTTCTTAGATTTCTG	9921
rs141417887	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120571602	GGATTTAGTCCTCAG[A/G]TGTTACTGTAGACGT	9921
rs141682432	snp	A/G	0.00517822	0.0506191	intron-variant	RNF10	GRCh38.p7	12:120568899	AGTGCTGGGATTCCA[A/G]GTGTGAGCCACTGTA	9921
rs141693740	snp	C/T	0.00636936	0.0560724	intron-variant	RNF10	GRCh38.p7	12:120556596	AATGTATAAAATCAT[C/T]TGAGAATGACATAGC	9921
rs141785696	snp	A/T	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120554509	GCAGAAGAAAACAGT[A/T]CATGGATTTAGACTT	9921
rs141790207	snp	A/G	0.00676609	0.0577691	intron-variant	RNF10	GRCh38.p7	12:120554222	ATTTTTCTATTTTTA[A/G]TAGAGATGGGGTTTC	9921
rs141862202	snp	C/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120559852	AGGCGCCCGTCACCA[C/T]GCCCAGCTAATTTTT	9921
rs141882801	snp	A/G	1.66868e-05	0.00288845	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120565485	GGGAGGAACGCCGCC[A/G]AGAGCGCAGGATTGA	9921
rs141915839	snp	A/G	1.65081e-05	0.00287293	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546551	CCTCAAAGGGGCGGC[A/G]GCAGCAGCAAACTCT	9921
rs142141596	snp	C/G	0.00478085	0.0486577	intron-variant	RNF10	GRCh38.p7	12:120536169	GCTCATGCCTGTAAT[C/G]CGAACACTTTGGGAG	9921
rs142173135	snp	G/T	0.00318978	0.0398085	intron-variant	RNF10	GRCh38.p7	12:120569880	ACATACTGTCTTTTC[G/T]GAAAGCTGCTTTTTG	9921
rs142236423	snp	A/G	0.00358779	0.0422022	intron-variant	RNF10	GRCh38.p7	12:120573529	TCAAACTATTTGGAT[A/G]CTGTCTCAGTCCATT	9921
rs142248705	snp	A/T	0.00358779	0.0422022	intron-variant	RNF10	GRCh38.p7	12:120537340	CTTCTGTAAAAACTC[A/T]TGTAGGCCGGGTGCG	9921
rs142258983	snp	C/G	0.00795532	0.062565	intron-variant	RNF10	GRCh38.p7	12:120540946	CCGCAACCTCCACCT[C/G]CCGGGTTCAAGCTAT	9921
rs142308916	in-del	-/TTAA	0.0433465	0.140692	intron-variant	RNF10	GRCh38.p7	12:120558995	TGGCAATAATTACTT[-/TTAA]TTAATTAAATTCATT	9921
rs142405808	snp	C/G	0.000977559	0.0220867	missense, splice-acceptor-variant, nc-transcript-variant	RNF10	GRCh38.p7	12:120563346	GAGTTTGCTGCAACA[C/G]GGTGTGCTGGAGTAT	9921
rs142525943	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120553209	TTGCCTCAGCCTCCC[A/G]AATAGCTGGGACTAC	9921
rs142630143	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120547985	AGATATTACTTCCAT[A/G]TAGAGCCAAGACTTT	9921
rs142745942	snp	C/T	0.00438332	0.0466095	intron-variant	RNF10	GRCh38.p7	12:120560480	TTCTGATATTACATA[C/T]AATGCTGTAACAATA	9921
rs142752056	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120564871	TACAAACCAAAAATA[A/G]CTGGATTTGGTTGCT	9921
rs142763100	snp	A/G	4.94368e-05	0.00497152	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557315	GTGCCATCTTGCCCA[A/G]TATGCCTCTATCCAC	9921
rs142848642	snp	C/T	0.00755907	0.0610114	intron-variant	RNF10	GRCh38.p7	12:120570916	TTCAAAAGCAAAGAC[C/T]TTTCTTACAGTTGGA	9921
rs142886432	in-del	-/TTTGGAGAGAATGACATC	0.379158	0.214052	intron-variant	RNF10	GRCh38.p7	12:120543001	TTTTAGGTGGTCAGG[-/TTTGGAGAGAATGACATC]TCATTTATACAGTGA	9921
rs142900172	snp	A/G	0.0785177	0.181917	intron-variant	RNF10	GRCh38.p7	12:120556263	ACTCTCGCCGGGCGC[A/G]GTGGCTCACGCCTAT	9921
rs142970792	snp	C/T	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120566087	GAACTGAGTCCTTGG[C/T]CCAGAAAAGGACTTC	9921
rs143053960	snp	A/G	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120542574	TATTTGTTTTTTGAG[A/G]CAGAGTCTCACTCTG	9921
rs143229921	snp	A/G	0.00795532	0.062565	intron-variant	RNF10	GRCh38.p7	12:120548378	GAACCTCTGAGTCTG[A/G]ATAAGAAACCAGCAG	9921
rs143295112	snp	C/G	0.0107246	0.0724382	intron-variant	RNF10	GRCh38.p7	12:120552333	TGAACCTGGGAGGCA[C/G]AGGTTGCAGTGAGCC	9921
rs143322499	in-del	-/GAATT	0.25634	0.24992	intron-variant	RNF10	GRCh38.p7	12:120567968	TAAATGTATAGAAAA[-/GAATT]GAAGGCCAGGCACGG	9921
rs143456860	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120565832	CCATCGTTCCCCATG[C/G]TCTCTGGATCACTGA	9921
rs143473515	snp	A/C	0.136506	0.222754	intron-variant	RNF10	GRCh38.p7	12:120541520	GCTCACTGCTAGCCC[A/C]GCCTCCCGGGTTCAC	9921
rs143542654	snp	C/G/T	3.29779e-05	0.00406055	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120560843	CAGAGGAGAAGCACA[C/G/T]TCCCGAGTCCTGCTT	9921
rs143647396	snp	C/T	0.0023933	0.0345097	intron-variant	RNF10	GRCh38.p7	12:120562742	AGATTCTAAGCAGAT[C/T]CCAATCCTTAGTGGG	9921
rs143719101	snp	G/T	0.00082462	0.0202887	intron-variant	RNF10	GRCh38.p7	12:120566815	TACAAGGGTTATCTT[G/T]CCTTTGCAGACCCAG	9921
rs143720189	snp	C/T	0.00358779	0.0422022	intron-variant	RNF10	GRCh38.p7	12:120558798	CTAGTCTCGAACTCC[C/T]GAGCTCAAGTGATCT	9921
rs143857913	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120555614	TGCCTCAGCCTCCCG[A/T]GTAACTGGGACTACA	9921
rs143862424	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120565922	TCTGATAAGATGGAA[A/G]TTTTGATAGACTAGG	9921
rs143912154	snp	A/G	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120546205	TGAGGGAGGGGACCC[A/G]TTAGGCTTCATTATT	9921
rs143915915	snp	A/T	0.0244538	0.107838	intron-variant	RNF10	GRCh38.p7	12:120549529	GTGGCTCACAGCTGT[A/T]ATCCCAGCACTTTGG	9921
rs144013875	snp	C/T	0.0170251	0.090679	intron-variant	RNF10	GRCh38.p7	12:120560212	GCTGGAATGCAGTGG[C/T]ATGATCTTGGCTCAC	9921
rs144046411	snp	C/G	0.000955047	0.0218314	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120565146	CTGTGAACTGGCTTT[C/G]CAACCTCCTGTGGTC	9921
rs144230392	snp	C/T	0.00636936	0.0560724	intron-variant	RNF10	GRCh38.p7	12:120556880	ATACAAAGCCAGGCG[C/T]GGTGGCTCACGCCGG	9921
rs144267571	snp	A/G	0.0352966	0.128072	intron-variant	RNF10	GRCh38.p7	12:120574755	ACATGGAGAAACCCC[A/G]TCTTTACTAAAAATA	9921
rs144316613	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RNF10	GRCh38.p7	12:120532412	GTGAGCCACCGTGCC[C/T]GGCCCCATATGCATG	9921
rs144325199	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120538805	ATTTTGAGGTTGGTG[C/G]TATGAAGCACTGCCC	9921
rs144374907	snp	A/C	0.000131828	0.00811768	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120546463	TGAACTTTCCTACCC[A/C]AAAAATGAAAGTTTT	9921
rs144434374	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120537998	TCTGATGCAGTGACT[C/T]CACGATGAGATGGTT	9921
rs144473739	snp	C/G	0.0189856	0.0955633	intron-variant	RNF10	GRCh38.p7	12:120544198	CGCCACTGCACTCCA[C/G]CCTGGGCAATAGAGT	9921
rs144536329	snp	A/G	0.000131791	0.00811655	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120557413	ACTGAGTGAGAAGAC[A/G]TGGAGTAAATGTCCC	9921
rs144576807	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120546187	CTACGCTGTGTTTGT[-/T]TTTGAGGGAGGGGAC	9921
rs144581855	snp	A/G	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120547766	ATCAGATCATGTGGG[A/G]CTTTGAAGGACTTTG	9921
rs144584909	in-del	-/AT/TAT/TT			intron-variant	RNF10	GRCh38.p7	12:120558577	ATATGTATATATATA[-/AT/TAT/TT]TTTTTTTTTGAGACA	9921
rs144595102	snp	C/T	0.0162398	0.0886349	intron-variant	RNF10	GRCh38.p7	12:120542155	ACAGGCGTGAGCCAC[C/T]GTGCCTGGCCTTTTT	9921
rs144648484	snp	A/G	0.00438332	0.0466095	intron-variant	RNF10	GRCh38.p7	12:120574876	GGTTGCGGTAAGCCA[A/G]GATTTGCGCCATTGC	9921
rs144698671	snp	A/G	0.0217236	0.101931	intron-variant	RNF10	GRCh38.p7	12:120554157	TGATTCACCTGCCTC[A/G]GCCTCCCAAAGTGCT	9921
rs144767915	in-del	-/TTT	0.378568	0.214407	intron-variant	RNF10	GRCh38.p7	12:120540869	TGCCAGTTTACTTTC[-/TTT]TTTTTTTTTTTTTTG	9921
rs144898588	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120554629	TAATGGCCTGCATTT[C/G]ATTTCTAAGTGAATA	9921
rs144944835	snp	A/G	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120561051	GCAGAGAATGGCTAA[A/G]AAAGCCAATTTGTTT	9921
rs145039001	in-del	-/GGGT			intron-variant	RNF10	GRCh38.p7	12:120567860	AGCATTTCATTATGG[-/GGGT]GTGTGTGTGTGTGTG	9921
rs145275147	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120574967	GTACTAGGCCGGGCA[C/T]AGTGGCTCACGCCTA	9921
rs145288520	snp	C/T	0.0232847	0.105357	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577001	TGAGATGCATTAGAG[C/T]AGTCCAACCCAGAAT	9921
rs145343225	snp	C/T	6.58935e-05	0.00573955	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563042	TGATGGCTCCCTTGG[C/T]GAAGGAGTCTGTTTT	9921
rs145347413	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120561800	ATAATACGTTGCAGC[C/T]GTATTTGTTCAAATG	9921
rs145382209	snp	C/T	0.00358779	0.0422022	intron-variant	RNF10	GRCh38.p7	12:120543993	AGTACTTTGGGAGGC[C/T]GAGGTGAGTGGATCA	9921
rs145527012	snp	A/G	0.0283406	0.115616	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576904	TCTCTTCCTGCCAAG[A/G]TTTTTAGTTCATTGC	9921
rs145695976	snp	A/G	3.29484e-05	0.00405871	synonymous-codon, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575877	TGTGCCCAGTTTTCA[A/G]AATTCCTTCAGCCAA	9921
rs145708971	snp	A/G	0.00438332	0.0466095	intron-variant	RNF10	GRCh38.p7	12:120535577	TTACTTGTAAAGGTA[A/G]GTGGAGGTAATATAA	9921
rs145736802	snp	G/T	3.3054e-05	0.00406521	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563392	GAAGAAACCACGGAA[G/T]TTTGTTCTCTGGACA	9921
rs145779566	snp	A/G	0.000164815	0.00907637			GRCh38.p7	12:120552654	GGGAAAGAGGAACAA[A/G]TGGGGACATAAGCCT	9921
rs145813848	snp	C/T	0.00398564	0.0444627	intron-variant	RNF10	GRCh38.p7	12:120557852	AGAGAGTAGATTAAT[C/T]ATTGGTTTCAAGTTT	9921
rs145862827	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120555665	GCTAATTTTTTTTTG[G/T]ATTTTTTTTTAGTAG	9921
rs145867367	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577328	TGTAACTCACGAAGC[C/T]CTGAGACCTGCTACC	9921
rs145888745	snp	C/T	0.00279162	0.0372561	intron-variant	RNF10	GRCh38.p7	12:120536417	TGGGTAACAGAGACC[C/T]CCATCTCTAAACAGT	9921
rs146023397	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120554309	GCCTCCCCAAGTGCT[A/G]GGATTACAAGTGTGA	9921
rs146144762	snp	C/T	0.0337553	0.125452	intron-variant	RNF10	GRCh38.p7	12:120569713	CTGCTAATTTTTGTA[C/T]TTTTAGTAGAGATGG	9921
rs146236915	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120554577	GCTCAGAACTGAGGC[C/T]GAGGTCCTAGTGCAG	9921
rs146297351	snp	A/G	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120566832	CTTTGCAGACCCAGA[A/G]GTCCACATTCCCCTC	9921
rs146309808	snp	C/G/T	0.000148254	0.00860859	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120562964	GGGAAGAGGCTCTGT[C/G/T]GGGATTGGCCGGAAG	9921
rs146363950	snp	C/T	0.0170251	0.090679	intron-variant	RNF10	GRCh38.p7	12:120570335	GGGATTACAGGTGCC[C/T]GCCACCATGCCCAGC	9921
rs146367061	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120573629	ATGACTCTGCTGGCT[G/T]GAGGACTGGGCATCT	9921
rs146385121	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120537563	AAACCGGGAGGCGGA[A/G]GTTGCAGTAAGCCAA	9921
rs146484374	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120548059	TTTTGGCATAAGCCC[A/G]ATTCAGGTACCTTTT	9921
rs146566206	snp	A/G			upstream-variant-2KB	RNF10	GRCh38.p7	12:120532841	TAAACGAAATTGTTT[A/G]TCTGACCTTCTGAGA	9921
rs146667323	snp	A/G	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120548760	CGCTCTTGGGTTCAC[A/G]CCATTCTCCTGCCTC	9921
rs146685862	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120552447	TTTGGGTTTCTGCTA[C/T]AAATCAGTGTCATCC	9921
rs146788376	snp	A/G	0.0372196	0.131242	intron-variant	RNF10	GRCh38.p7	12:120562466	TTTAGTAGAGATGGG[A/G]TTTCTCCATGTTGGT	9921
rs146802529	snp	C/T	0.000165134	0.00908513	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120546418	AGATGGAAAGAACTC[C/T]AGTGGATCCAAGCGT	9921
rs146826529	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120567040	ATGCAAAGCTTTGGT[A/G]TCTGAGTTTACAACC	9921
rs146861677	snp	A/C	0.0138799	0.0821421	intron-variant	RNF10	GRCh38.p7	12:120555612	CCTGCCTCAGCCTCC[A/C]GAGTAACTGGGACTA	9921
rs146996951	snp	C/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120571608	AGTCCTCAGATGTTA[C/T]TGTAGACGTACCCAG	9921
rs146999993	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120535867	AGTCACTGACTTGTC[C/T]ACCAGGGTGAAATTG	9921
rs147264429	snp	C/T	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120550081	TTTTCTAGCTGCCTG[C/T]GCTAGAGAAGTAAAA	9921
rs147344253	in-del	-/ACTC			intron-variant	RNF10	GRCh38.p7	12:120537973	GCTACTACAGCAGAT[-/ACTC]AGGAGCTCTGATGCA	9921
rs147354400	snp	C/T	0.00795532	0.062565	intron-variant	RNF10	GRCh38.p7	12:120560500	CTGTAACAATAAACG[C/T]GTGACTAAAGTTTTG	9921
rs147370516	snp	C/G/T	0.000477925	0.0154512	missense, synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120565174	GTCTCTAAGGAAACC[C/G/T]TAGAGATGTTCTCAG	9921
rs147386656	snp	C/T	0.0391387	0.134304	intron-variant	RNF10	GRCh38.p7	12:120550757	GCCCGCCACCATGCC[C/T]AGCTAATTTTTTGTA	9921
rs147613084	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120571637	AGGAAAGAGGCCAAG[A/C]ATAGCTGAGGCAGAA	9921
rs147632591	snp	C/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120540904	TTGTTGCCCAGGCTG[C/G]AGTGTAGTGGTGCAG	9921
rs147661957	snp	A/G	0.0103295	0.0711199	intron-variant	RNF10	GRCh38.p7	12:120544176	AGGTTGCAGTGAGCC[A/G]AGATTGCGCCACTGC	9921
rs147730561	in-del	-/AAAA	0.0755793	0.179102	intron-variant	RNF10	GRCh38.p7	12:120558455	AAATGTGTATTAATT[-/AAAA]AAAAATCCTCAGATA	9921
rs147753889	snp	C/T	0.00676609	0.0577691	intron-variant	RNF10	GRCh38.p7	12:120555542	GCCCAGGCTGGAGTA[C/T]AGTGGTGCAATCTTG	9921
rs147768290	snp	A/C	0.00026357	0.0114767	missense, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575896	TCCTTCAGCCAAGCT[A/C]TTGAAGCAGCCTTCA	9921
rs147770115	snp	G/T	0.00478085	0.0486577	intron-variant	RNF10	GRCh38.p7	12:120557011	TAGCTGAGCGTGGTG[G/T]CAGGCGCCTGTAGTC	9921
rs147859998	snp	C/T	0.00755907	0.0610114	intron-variant	RNF10	GRCh38.p7	12:120571527	AAAGGAGAGACTTAA[C/T]AGGCTAATGTTGCAC	9921
rs147876361	snp	C/T	0.0364509	0.129988	intron-variant	RNF10	GRCh38.p7	12:120574914	CCTGGGCAACAAGAG[C/T]GAAACTCCATCTCGA	9921
rs147936384	snp	A/G	0.000230597	0.0107352	missense, utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120575659	GAAAAGCAAAAGCAG[A/G]TGTGTGGCCCAAAAC	9921
rs148043070	snp	A/G	8.24042e-05	0.00641836	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557662	AATGGATGAATGTAG[A/G]CCATCCCATTCATCT	9921
rs148143877	snp	C/T	0.00438332	0.0466095	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577501	TTGAGCTGAATTTGA[C/T]GTGAATTCTTTTGCT	9921
rs148229374	snp	C/G	0.00279162	0.0372561	intron-variant	RNF10	GRCh38.p7	12:120536532	GGATATGGCAAACTT[C/G]TTTACCTGGTGTGAG	9921
rs148232308	snp	A/G	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120560343	ATCTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	9921
rs148356990	snp	C/T	0.0185938	0.0946107	intron-variant	RNF10	GRCh38.p7	12:120545705	ACCATGCGCGGCTAA[C/T]TTTTTGTATTTTTAA	9921
rs148444919	snp	A/G	0.0755793	0.179102	intron-variant	RNF10	GRCh38.p7	12:120556448	AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGATG	9921
rs148477214	snp	A/G	0.0325976	0.123435	intron-variant	RNF10	GRCh38.p7	12:120547959	GAGGTGGTGAGAGAC[A/G]TTAAGATTTGAGATA	9921
rs148508902	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120559520	GTCCTGAGTAGCTGA[A/G]ATTACAGGCACGCAC	9921
rs148578113	in-del	-/AAA			intron-variant	RNF10	GRCh38.p7	12:120557086	GAGATGGACCGTCTC[-/AAA]AAAAAAAAAAAAAAG	9921
rs148586638	in-del	-/A	0.0729998	0.176553	intron-variant	RNF10	GRCh38.p7	12:120548363	TAGGTTCAAGAACTG[-/A]AACCTCTGAGTCTGG	9921
rs148604245	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120555260	GATCTTGGCTCACTG[C/T]AACCTCTGCCTCCAG	9921
rs148713329	snp	A/G	0.0785177	0.181917	intron-variant	RNF10	GRCh38.p7	12:120569781	GGCTTCAAGTGATCC[A/G]CCTGCCTCGGCCTCC	9921
rs148739063	snp	C/T	0.0755793	0.179102	intron-variant	RNF10	GRCh38.p7	12:120574782	AATACAAAAATTAGC[C/T]GGGCGTGGTGGTGCA	9921
rs148757034	snp	C/T	0.00279162	0.0372561	intron-variant	RNF10	GRCh38.p7	12:120538887	CTGCCTTGAAGAATG[C/T]CTCTGAGCTGTAAAT	9921
rs148836482	snp	A/G	8.23839e-05	0.00641757	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120576652	TTCAGCACCTCAGTC[A/G]TCCACACCAAGTGAC	9921
rs148849373	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576914	CCAAGGTTTTTAGTT[A/C]ATTGCCAGTTTAGTC	9921
rs148852812	snp	A/G	0.00279162	0.0372561	intron-variant	RNF10	GRCh38.p7	12:120541372	GTGATGTGAAATGGA[A/G]TTAAGGAAAGCAAAG	9921
rs148914216	snp	A/C	0.0185938	0.0946107	intron-variant	RNF10	GRCh38.p7	12:120535606	AATTAAATAAACTTA[A/C]AAAACTAATTAAAAA	9921
rs148974387	snp	C/T	0.0329836	0.124112	intron-variant	RNF10	GRCh38.p7	12:120557883	GTTTAATCTATACAT[C/T]CTAATTTTTCATTTT	9921
rs149001705	snp	A/C/T	0.00478085	0.0486577	intron-variant	RNF10	GRCh38.p7	12:120549506	AGTGGGTGATGGGGC[A/C/T]GGGCGCAGTGGCTCA	9921
rs149061940	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120571678	GAATATTTTAAAAAT[C/G]ATTTGATAACTTGTG	9921
rs149113802	snp	G/T	0.00279162	0.0372561	intron-variant	RNF10	GRCh38.p7	12:120567807	CAAGAATAAATGTTC[G/T]TGGGTTTTAAAAAAA	9921
rs149220464	snp	C/T	0.0788843	0.182262	intron-variant	RNF10	GRCh38.p7	12:120551541	TGACCTCAGGTGATC[C/T]GCCTACCTCAGCCTC	9921
rs149375899	snp	A/G	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120554050	GCTGGGACTACAGGC[A/G]CGTGTCACCATGCCC	9921
rs149497258	snp	C/T	8.23608e-05	0.00641667	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563871	CCTCGTGCGGGAGTA[C/T]GGCAGCCTGGAGAGG	9921
rs149593517	snp	C/G	0.00557542	0.0525036	intron-variant	RNF10	GRCh38.p7	12:120573972	TTTCAGGAATGAATG[C/G]GAGAATAGGTCTCCC	9921
rs149749031	snp	A/G	0.0107246	0.0724382	intron-variant	RNF10	GRCh38.p7	12:120570991	CTTCCCTCTTCCTGT[A/G]CCGGTCGCTGATTTC	9921
rs149778618	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120535328	ACTAAGTTGTTCTAC[C/T]CTTTAATGTTGAATT	9921
rs149816443	snp	C/T	0.000164745	0.00907442	missense, synonymous-codon, nc-transcript-variant, intron-variant	RNF10	GRCh38.p7	12:120571236	CCAGTCAGGGCAGTC[C/T]CTCATTCTGCGTTGG	9921
rs149995353	snp	A/T	0.0372196	0.131242	intron-variant	RNF10	GRCh38.p7	12:120567496	TCACGAGGTCAGGAA[A/T]TCAAGACCAGCCTGA	9921
rs150043680	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120561719	CTGGTATTTGAATTC[C/T]CTTCTCCCTGACTCC	9921
rs150118608	snp	A/G	0.000576431	0.0169671	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575714	TCCACTGGTGAAGGG[A/G]GAGTTTGGCTTCTTT	9921
rs150150750	snp	A/G	0.000196522	0.00991071	intron-variant	RNF10	GRCh38.p7	12:120563299	TGCCACATTGCTTTC[A/G]GAAAGCAGGAGATAT	9921
rs150275640	snp	C/T	0.0111196	0.0737302	intron-variant	RNF10	GRCh38.p7	12:120548965	ATGAGCCACCGCGCC[C/T]GGCTGAGGGATTTTA	9921
rs150282383	snp	A/G	0.000148447	0.00861404	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120546544	GATGCCTCCTCAAAG[A/G]GGCGGCGGCAGCAGC	9921
rs150306336	in-del	-/A			intron-variant	RNF10	GRCh38.p7	12:120537146	GAGACCCTGTCCTAC[-/A]AAAAAATAAATGAGC	9921
rs150327340	snp	A/G	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120544659	AAACCTTGTCTCTAA[A/G]TAAATAAAGTGCATA	9921
rs150334309	snp	C/T	6.86742e-05	0.00585939	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563587	AAGTCAGGCTTCACA[C/T]GCCTCAGCAGCTCTC	9921
rs150416049	snp	C/T	0.00438332	0.0466095	intron-variant	RNF10	GRCh38.p7	12:120555977	TATTTTCATTAGAGA[C/T]GGGGTTCCACCGTGT	9921
rs150463542	in-del	-/C			intron-variant	RNF10	GRCh38.p7	12:120559984	TGAGCCACCACACCC[-/C]AGCTGGCTTGGTCTT	9921
rs150527064	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120556769	TTGTCACTTTTTTCT[A/G]TTTAATGTAGAACCC	9921
rs150600491	snp	A/G	0.00494288	0.0494672	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120560730	CATTCTTATAGATGA[A/G]CAGCACAGCCAGTAC	9921
rs150629669	snp	A/C	0.000153988	0.00877328	missense, nc-transcript-variant, intron-variant	RNF10	GRCh38.p7	12:120571192	TGGTTCCCTTTCAGA[A/C]TTTCTGCTGACCCCT	9921
rs150729346	snp	A/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120537113	TGAGGCAGGCCGATT[A/T]CTTGAGCCCAGGAGT	9921
rs150874060	snp	A/G	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120546001	GAATCTGGTTATGTT[A/G]TAGTAATTTAAAAAG	9921
rs150896248	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120561435	TGAGATATTGATTGC[A/G]TAGGTTAAGCTCAGT	9921
rs151036584	snp	C/T	0.00279162	0.0372561	intron-variant	RNF10	GRCh38.p7	12:120570943	TGGAGTAGATTCTAC[C/T]ATGACTTCTAGAGTT	9921
rs151072838	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120558903	GTCCACAGAATTTTC[A/G]TTAATGAACATACCA	9921
rs151251189	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120540491	AGTTTTTCCCATGTA[C/T]ATCCTGGCAAGTTGT	9921
rs151315852	snp	A/G	1.65441e-05	0.00287607	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563388	CGATGAAGAAACCAC[A/G]GAAGTTTGTTCTCTG	9921
rs180704096	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120540933	AGTCTCGGCCTTGCC[A/G]CAACCTCCACCTCCC	9921
rs180711859	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120559275	CAACCTCCACCTCCT[C/T]GGTTCAAACGATTTT	9921
rs180721199	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120549401	ATTTGTTAGCCCTGT[G/T]TGTCTGCTGCAGGGC	9921
rs181009144	snp	A/G/T	0.00398763	0.0445073	intron-variant	RNF10	GRCh38.p7	12:120545482	CAGGCATGAGCCACC[A/G/T]CGCCTGGCCATTTTT	9921
rs181027048	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120553795	CTTTTGTTTCCTTTT[A/G]TGTGGCCCTAGTCAT	9921
rs181029139	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120572664	GCAATGGCGTGATCT[C/T]GGCTCACTGCAACCA	9921
rs181056468	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120536953	CTGCTATGTCCTTCA[C/T]TTTGAATATGTTGGT	9921
rs181074635	snp	C/T	0.00358779	0.0422022	intron-variant	RNF10	GRCh38.p7	12:120564303	ACTCTTTGAGTACTA[C/T]AAATTTTTCATCAAA	9921
rs181206732	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120558902	TGTCCACAGAATTTT[C/T]GTTAATGAACATACC	9921
rs181208654	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120539994	TGTCCACCACCACAC[C/T]GGCCTAATTTTTGTA	9921
rs181341161	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120569461	ACTGCACTACTGTGA[C/T]GCTCTTCTGCTTAAC	9921
rs181353831	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120550509	AGAGCCATGTGGAGA[C/T]GAAAAATAAGGGATG	9921
rs181462500	snp	C/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120572313	CCTCGTGATCCGCCT[C/G]CCTCAGCCTCCCAAA	9921
rs181472536	snp	A/C/G	0.00438332	0.0466095	intron-variant	RNF10	GRCh38.p7	12:120536614	ACTGATTTTGCAGTT[A/C/G]TGCACATGCGTAGCT	9921
rs181480164	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120553370	TGGGATTACAAGCAT[A/G]AGCCACCATGCCCAG	9921
rs181488456	snp	G/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120565274	GGGGAGGAAACTTAT[G/T]GAACTGTATCATGAG	9921
rs181631901	snp	A/G	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120546708	ACAAGAGGTAGAGGA[A/G]TAGATAATCAAAGCA	9921
rs181653093	snp	A/T	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120559699	GGTGTTATTTTTTTT[A/T]AATTTTATTTTTTGA	9921
rs181807216	snp	A/G	0.000253158	0.0112479	intron-variant	RNF10	GRCh38.p7	12:120546380	TCAGCTTCTTAAGAC[A/G]TTCTTTTGTGTTTCT	9921
rs181882299	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120550063	CATGTGTGTAATCAT[A/G]CATTTTCTAGCTGCC	9921
rs181953705	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120564894	TGGTTGCTTATTCCA[C/T]CTTGCTGTAGGTTGA	9921
rs182100034	snp	C/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120569688	GGATTACAGGCAGCA[C/G]CACCATACCCTGCTA	9921
rs182110104	snp	C/T	0.00398564	0.0444627	intron-variant	RNF10	GRCh38.p7	12:120550627	TTTTGGACGAAGTCT[C/T]GCTCTGTCGTCCAGG	9921
rs182166011	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120568803	AGAGATAGGGTCTTG[C/T]TCAGTGCTGTGATGC	9921
rs182286901	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120543285	GGTGAGGCCTGAGCA[G/T]AGGAATTCCGTAAAA	9921
rs182359641	snp	A/G			upstream-variant-2KB	RNF10	GRCh38.p7	12:120532692	TAAAATTTAGTTATT[A/G]AGAAGATTAAATGTG	9921
rs182410283	snp	C/T	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120566265	TTCACCTTTTTATTA[C/T]GGAAATATCAAGACA	9921
rs182423221	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120547893	AGACTAAGAGACTAC[A/C]AAGATATTCTTGGTG	9921
rs182565555	snp	A/G	0.0785177	0.181917	intron-variant	RNF10	GRCh38.p7	12:120570165	GCTGGGATTACAGGC[A/G]TGAGCCACCACACCC	9921
rs182574759	snp	C/G	0.00557542	0.0525036	upstream-variant-2KB	RNF10	GRCh38.p7	12:120534282	CGAGACCCGGATGTA[C/G]GCAAAAACTACATTT	9921
rs182688625	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120556394	AAATTAGCCCGGCGC[A/G]GTGGCGGGTACCTGT	9921
rs182716986	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120538268	CCCCCTTTTCTACCT[C/T]GTGGAAGAAAGCCCT	9921
rs182719975	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120555646	GCACGCACCACCACT[C/T]CCAGCTAATTTTTTT	9921
rs182883272	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120574654	TACTTGGCTGGGCAC[A/C/G]GTGTCTCATGCCTGT	9921
rs182949599	snp	C/T	0.0023933	0.0345097	intron-variant	RNF10	GRCh38.p7	12:120575273	ACTCACTGCTTCCTC[C/T]GACAGCTCGATGTTT	9921
rs182986988	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120538837	GGCATTCTTCCTGTT[A/G]TTCTGGTACCAGAAA	9921
rs183017297	snp	A/C	0.00557542	0.0525036	intron-variant	RNF10	GRCh38.p7	12:120541209	TGGCTTTACCTAAAT[A/C]TATGCAAACCGTGAG	9921
rs183094494	snp	A/G/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120542146	GCTGGGATTACAGGC[A/G/T]TGAGCCACCGTGCCT	9921
rs183335877	snp	A/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120560098	ATTTCTTTATTCTTT[A/T]TTGTTGGTTTTACTG	9921
rs183419563	snp	C/T	3.29544e-05	0.00405908	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120566891	ATTCTTATACCTGCT[C/T]CTCTGATTCTGCTTT	9921
rs183455415	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120548242	GTTAACTGTGAATCA[A/G]CAGTCAAGGAAGAGA	9921
rs183571874	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120551375	TCTTGGCTCACTGCA[A/G]CCTCTGCCTCTCGGG	9921
rs183578406	snp	A/G	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120564566	GGAGATCAAGTCTGC[A/G]GTGAGCTGGCCTGGG	9921
rs183588138	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120545791	TGATCCACCTGCCTC[C/G]GCCTTCCAAAGTGCT	9921
rs183601309	snp	A/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120570985	GAAGCTCTTCCCTCT[A/T]CCTGTACCGGTCGCT	9921
rs183721702	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120549040	GGTGAGAGGCAAAGT[C/G]ATGTGGGGAAAAGGG	9921
rs183780731	snp	A/T	0.00358779	0.0422022	intron-variant	RNF10	GRCh38.p7	12:120569892	TTCTGAAAGCTGCTT[A/T]TTGTTTTGTTTTGTT	9921
rs183811943	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF10	GRCh38.p7	12:120532866	CTGAGAAATCATCAA[A/G]TCCCCAAACTGGTCA	9921
rs183881292	snp	C/G	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120568206	GCCCAGATTGGGCCA[C/G]TGCACTCTAGCCTGG	9921
rs183949258	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120573385	ATGGCCAGTTGTTTT[A/G]TAGAATATCCTACAG	9921
rs183978494	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120537733	ACCATGTTTGCCACC[A/G]CCAGTGTCTGCTTTT	9921
rs184077395	snp	A/C	3.7723e-05	0.00434282	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534904	CTCTTCGGGCAGCAG[A/C]AAAGGGCAACAGCCG	9921
rs184126441	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120554463	AATTTTAGTTCAAGG[A/G]ATGCCTTTGGGGAAT	9921
rs184325047	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120535472	GTCATCCTTCAGTGG[A/C]TATTCATTGTGGGGT	9921
rs184435469	snp	G/T	0.000102258	0.00714973	intron-variant	RNF10	GRCh38.p7	12:120552707	AGGCCAAGTGAGTAT[G/T]GCTACCCCTCAGAGG	9921
rs184489305	snp	C/T	0.0023933	0.0345097	intron-variant	RNF10	GRCh38.p7	12:120557962	TCTGTGGTCAGCCAG[C/T]CTTGGTGCCTGTCGT	9921
rs184495200	snp	A/T	0.000399281	0.0141238	downstream-variant-500B	RNF10	GRCh38.p7	12:120577603	ATTGTGAGCTTTTTG[A/T]TTTTTTAAGTTCATT	9921
rs184499256	snp	C/G	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120539776	TCCATTTTGGAATGT[C/G]TCTTGACAGTAGTTC	9921
rs184628600	snp	G/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120559000	ATAATTACTTTTAAT[G/T]AATTAAATTCATTAA	9921
rs184651890	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120543994	GTACTTTGGGAGGCC[A/G]AGGTGAGTGGATCAC	9921
rs184726883	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120568372	TTGTCTTATATATAA[A/C]GAATGTTTAAAGTGT	9921
rs184824019	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120544717	ATAAATCGGTGTAAC[C/G]GTTCTAGAAAGCAAC	9921
rs184918703	snp	A/G	1.64776e-05	0.00287028	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563930	TGGAGATTGCTGGCT[A/G]CTCCATGTCTGAGGT	9921
rs184970946	snp	C/T	0.00557542	0.0525036	intron-variant	RNF10	GRCh38.p7	12:120539111	AAACTGTGTGTCAGC[C/T]ACTATGGTAGGCATT	9921
rs185153375	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120567591	CTGTAGTCCCAGCTA[C/T]TTGGGAGGCTGAGGC	9921
rs185260077	snp	A/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120548483	CTGATAGGTTAAGAA[A/T]AGGACTGAAAGTTGA	9921
rs185391012	snp	A/T	0.00318978	0.0398085	intron-variant	RNF10	GRCh38.p7	12:120536379	GCGGTGAGCTATATC[A/T]CGATACTGCATACCA	9921
rs185448206	snp	C/T	0.0429648	0.14013	intron-variant	RNF10	GRCh38.p7	12:120553244	GCATACCACCACCCC[C/T]GTCTAATTTTTTTAT	9921
rs185561642	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120569515	TGTGGCAGATCATTA[A/G]ATACATTATTTGTGA	9921
rs185565042	snp	C/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120571367	TTATGGGAACCTCCT[C/G]CAGGGATTGTTACCT	9921
rs185575109	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120550568	CACAAGCAAACAGAA[C/T]GTGGAGAATGTGGCG	9921
rs185584125	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120576092	TAGTGTCATTTAAAT[A/C]ATACTCCATTTGGTA	9921
rs185589504	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120549902	TTTGGAGGTCCTAGT[A/G]GGGGTAAAGAATTGT	9921
rs185709486	snp	A/C	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120572318	TGATCCGCCTGCCTC[A/C]GCCTCCCAAAGAGCT	9921
rs185719637	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120536819	GGGCTCCTCTTTAAG[C/T]CACTAACATACATTC	9921
rs185725932	snp	C/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120553495	GCAAGCTCCACCTCC[C/T]GGAGCTTCATGCCAT	9921
rs185731363	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120557159	AGAAAGATATGTTGA[A/G]TATAAGGATGTACGG	9921
rs185782488	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120559845	GGATTATAGGCGCCC[A/G]TCACCACGCCCAGCT	9921
rs185803657	snp	A/G	0.0107246	0.0724382	intron-variant	RNF10	GRCh38.p7	12:120541651	ATGTTAGCCAGGATG[A/G]TCTCTATCTCCTGAC	9921
rs185890866	snp	A/C	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120572751	GGTTACAGGCGCCTA[A/C]CACCATGCCCGGCTA	9921
rs185902775	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120537162	AAAAAATAAATGAGC[C/T]GGGCGTGGTGGCACG	9921
rs186014449	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120554065	GCGTGTCACCATGCC[C/T]GGCTAATTTTTTTTG	9921
rs186127980	snp	C/G	0.00478085	0.0486577	intron-variant	RNF10	GRCh38.p7	12:120564916	GTAGGTTGACAGTTT[C/G]TCTTTGGCTTTTCAA	9921
rs186131861	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120537896	AGGTTAGGAAACTGG[A/G]TATTGGCTGATTTTT	9921
rs186140429	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120546386	TCTTAAGACGTTCTT[C/T]TGTGTTTCTTGCTTT	9921
rs186260817	snp	A/G	0.0138799	0.0821421	intron-variant	RNF10	GRCh38.p7	12:120541046	ATTTTTAGTAGAGAC[A/G]GGGTTTCTCCATGTT	9921
rs186268712	snp	A/G	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120559600	ATGTTGGCCAGCATG[A/G]TCTCAATCTCTTGAT	9921
rs186410648	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120540564	GGTCCCAGGCCTGAT[A/G]GTACCTTCAACCTTT	9921
rs186528528	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120547286	AGAAGCAAGGGAGCA[C/T]ACTATATGGTTGTTT	9921
rs186677657	snp	A/G	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120568850	CAGTCTTGAACTCCT[A/G]GGCTCAAGTGATCCT	9921
rs186687295	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120566404	TTTGGGTTTTAGCTT[C/T]TGTCTGCATCCTCTA	9921
rs186718142	snp	C/T	0.00557542	0.0525036	intron-variant	RNF10	GRCh38.p7	12:120547975	TTAAGATTTGAGATA[C/T]TACTTCCATATAGAG	9921
rs186763474	snp	A/T	0.00279162	0.0372561	intron-variant	RNF10	GRCh38.p7	12:120565718	GTCAAAGTGCCTAGC[A/T]CATAGTAAGGATTAA	9921
rs186843561	snp	A/G	0.0337553	0.125452	intron-variant	RNF10	GRCh38.p7	12:120570169	GGATTACAGGCGTGA[A/G]CCACCACACCCAGCC	9921
rs186860009	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120552039	TTTTGAGCTGAGGTC[A/G]CGCCACTGCACTCCA	9921
rs186910939	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120550371	GAAAGTGACAGTGGG[C/G]CAGCTAGGACAAGCT	9921
rs187041853	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120554634	GCCTGCATTTGATTT[C/G]TAAGTGAATAGATGA	9921
rs187060835	snp	A/G	4.94417e-05	0.00497176	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563015	GGCATTCTTATAGAT[A/G]AACAGCACAGCCAGT	9921
rs187166497	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120555893	TCTTGGGTTCAAGCA[A/G]TTCTCATGCCTCAGC	9921
rs187171378	snp	C/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120574757	ATGGAGAAACCCCGT[C/T]TTTACTAAAAATACA	9921
rs187175715	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120538432	CTACCAGGATTTTCT[C/T]GATCTTTCCGGCTAG	9921
rs187223741	snp	C/T	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120573487	GTGACATTTTGATTA[C/T]CTTTTAAGAGTAAAA	9921
rs187300824	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	RNF10	GRCh38.p7	12:120533632	TAAATGTAAGGTATT[A/G]TCATTATTAACGTTA	9921
rs187397476	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120550817	TAGCCAGGGTGGTCT[C/T]GATCTCCTGACCTCG	9921
rs187529557	snp	A/G	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120538901	GCCTCTGAGCTGTAA[A/G]TGGACCTGGAGATTT	9921
rs187587613	snp	C/G/T	0.00130835	0.0255437	missense, stop-gained, intron-variant, nc-transcript-variant	RNF10	GRCh38.p7	12:120563344	TAGAGTTTGCTGCAA[C/G/T]AGGGTGTGCTGGAGT	9921
rs187662092	snp	A/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120575369	AGTAAGAATCTCTTG[A/T]GCCTTCTGTGCAGTG	9921
rs187664300	snp	C/T	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120569734	GTAGAGATGGGGTTT[C/T]GCCATGTTGGCCAGG	9921
rs187717714	snp	A/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120567209	AGCTCTTTAGGCAGG[A/T]TAGTTGAAAATGGAG	9921
rs187830745	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120560222	AGTGGCATGATCTTG[A/G]CTCACTGCGACCTCT	9921
rs187957379	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120556395	AATTAGCCCGGCGCA[G/T]TGGCGGGTACCTGTA	9921
rs188043483	snp	G/T	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120562029	ACTTTTAAGTTCAGG[G/T]GTACAAATGCAGGTT	9921
rs188058790	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120543286	GTGAGGCCTGAGCAT[A/G]GGAATTCCGTAAAAG	9921
rs188123919	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120542793	TCTGGCCTCATGTGA[C/T]CTGCCTGCCTTGGCC	9921
rs188134870	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120548579	TTTACACAGTACTTT[G/T]CAGTGGCTTTGCTCT	9921
rs188220240	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120568271	AAAATACTGAGACAG[A/G]TGTGTTCCAAATTGG	9921
rs188236497	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120549394	TGGTTGTATTTGTTA[C/G]CCCTGTTTGTCTGCT	9921
rs188423977	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120567753	GAATGTAATTCTTCT[A/G]TTCACGTACTAATGG	9921
rs188466159	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120569946	CGCCCGGGCTGGAGT[A/G]CAGTGGTGCGATTTT	9921
rs188470768	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120544288	AACAGTTTGGAAGGC[C/T]GAGGCAGGATTGCTT	9921
rs188566584	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120551491	TTCAGTAGAGATGGG[G/T]TTTCACCATATTGCC	9921
rs188653337	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120553740	GACAATTGAATGACA[A/G]GTTGAAGTGCTTGGC	9921
rs188661169	snp	A/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120572420	ATGTAATTACAGCAG[A/T]TTGTACTGAGAAATA	9921
rs188665418	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120536824	CCTCTTTAAGCCACT[A/C]ACATACATTCATTAG	9921
rs188820344	snp	C/G	0.00279162	0.0372561	intron-variant	RNF10	GRCh38.p7	12:120539890	ACCCAGGCTGGAGTT[C/G]AGTGGCGCGATCTCA	9921
rs188863621	snp	C/T	9.88549e-05	0.00702977	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120576651	GTTCAGCACCTCAGT[C/T]GTCCACACCAAGTGA	9921
rs188903933	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120548283	AGAGCTGTCAGCATA[C/T]AGTTGGTGCTTAAAG	9921
rs189140269	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120553336	CTCGTGATCCACCTG[C/T]CTCGGCCTCCCAAAG	9921
rs189154321	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120536566	ATTGGAGTATGGGTT[C/T]TCGGGCCGTGTCAGG	9921
rs189241881	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120540760	CTGTCTTATCAGTGA[A/G]CATTTCTGTAAGCAT	9921
rs189248336	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF10	GRCh38.p7	12:120532759	CCCATTGTTTTGCAC[C/T]GAGCTTCAGCACAGT	9921
rs189286796	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120539528	CTTGCTGACTGGTAT[G/T]CTGACCTCTAGGCCG	9921
rs189294781	snp	A/G	0.00398564	0.0444627	intron-variant	RNF10	GRCh38.p7	12:120557169	GTTGAGTATAAGGAT[A/G]TACGGGGATAGAGAT	9921
rs189382081	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120564265	GAGAAATGTCACAAA[C/T]TTGTTGTAAGATTTA	9921
rs189449859	snp	A/G	0.00279162	0.0372561	intron-variant	RNF10	GRCh38.p7	12:120545886	TTCTGTCAATTTAAC[A/G]GCTTCTGAATTTGAC	9921
rs189515513	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120559238	CCAGGCTGGAGTGCA[A/G]TGGTGTGATCTCGGC	9921
rs189658253	snp	C/T	0.0752113	0.178743	intron-variant	RNF10	GRCh38.p7	12:120545342	GCCCGCCACCATGCC[C/T]GGCTAATTTTTTTTT	9921
rs189709762	snp	A/G	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120550469	TGGGGCATTAAGGGT[A/G]GAAGACCGTTTGATT	9921
rs189729268	snp	C/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120566676	CTGAGGTGGGAGGAT[C/T]GCTTGAGCCTGGGAG	9921
rs189744418	snp	G/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120548165	CTTCAGTTTGGAAAT[G/T]TTATATGTACATTGA	9921
rs189878978	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120569607	CACAAGGCACAATCT[C/T]GGCTCACTGCAACCT	9921
rs189895354	snp	C/T	0.0364509	0.129988	intron-variant	RNF10	GRCh38.p7	12:120550609	TTTTGTTTGCTTTTT[C/T]TTTTTTGGACGAAGT	9921
rs189947623	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120569379	CATATCATTTTGCAG[A/G]TTAGGAACCTGTGGC	9921
rs190042382	snp	C/G	0.00636936	0.0560724	intron-variant	RNF10	GRCh38.p7	12:120572151	GGCTTGCTGTAAGCT[C/G]CGCCTCCCGGGTTCA	9921
rs190381681	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120568648	GCCTGGCTAATTTTT[A/G]TATTTTTAATAGAGA	9921
rs190394640	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120559975	GTGCTGAACGTGAGC[C/T]ACCACACCCAGCTGG	9921
rs190518335	snp	A/G	0.0107246	0.0724382	intron-variant	RNF10	GRCh38.p7	12:120574355	CCTTTTAAGTGGCAT[A/G]TTTGCAGTTGGGGCT	9921
rs190523639	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120552856	CCCGCCCTTCCTTTC[C/T]TTTACCCACTTTCCA	9921
rs190528699	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120538035	ACAAAAGGGTACACT[C/T]AAGCTCCGCATAATC	9921
rs190537074	snp	C/T	0.00318978	0.0398085	intron-variant	RNF10	GRCh38.p7	12:120554872	AAGGCACTGTGGTGA[C/T]GCAGCAGCTGTTGGC	9921
rs190628450	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120549968	CCGGTCTGGACAACA[C/G]AATGCTCAAAGTTAA	9921
rs190783941	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120571129	AGGGCTCACTCATCT[C/T]TCTTGTTAAGGACAC	9921
rs190794306	snp	C/T	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120535693	CATAATGTCTATTGT[C/T]GTGTGTTGGACTATA	9921
rs190796793	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120542881	GTAAGGGTCACTGTC[C/T]GTAAGCAGGATTTAA	9921
rs190867730	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120541185	AATAAGCCCTTGCCA[C/T]GTAGAATCTGGCTTT	9921
rs190877390	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120559672	ACAGGTGTGAGCCAC[C/T]GTACTCCGCCTGGTG	9921
rs190923718	snp	A/G	0.00438332	0.0466095	intron-variant	RNF10	GRCh38.p7	12:120572820	TGGCCAGGCTGGTCT[A/G]GAACTCTTGACCTCA	9921
rs191051982	snp	A/G	0.00597247	0.0543191	intron-variant	RNF10	GRCh38.p7	12:120560374	GGTCAGGCTGGTCTC[A/G]AACTCTTGATCTCAA	9921
rs191128506	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120568283	CAGATGTGTTCCAAA[C/T]TGGTAGTAGTGTTAC	9921
rs191156539	snp	A/G	0.00835141	0.0640778	intron-variant	RNF10	GRCh38.p7	12:120565770	TAGTGGGTGATATAC[A/G]CCTGTTCCAGAGATG	9921
rs191282653	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120535293	GTTTGTGTGACTCAT[A/C]AGTCCACGCTCCTAA	9921
rs191291836	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120552399	AGTAAGACTCCGTCT[C/T]AAAAAAAAAAGCTGT	9921
rs191384629	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120547846	TAAGGTAACCTGATG[C/T]GGAGTTTTAAAGGGG	9921
rs191476230	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120570692	TATTACCTAGGGAGT[A/G]TTGGGGAAAAGTTTG	9921
rs191529559	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120542091	CAGGATGGTCTTGAT[C/T]TCCTGACCTCGTGAT	9921
rs191606987	snp	A/C	0.00914312	0.0669923	intron-variant	RNF10	GRCh38.p7	12:120548783	CCTGCCTCAGTCTCC[A/C]GAGTAGCTGGGACTA	9921
rs191618446	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120555933	AGCTGGGATTACAGG[C/T]GTGCACCACTATGCC	9921
rs191628034	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120574871	GCAGAGGTTGCGGTA[A/C]GCCAAGATTTGCGCC	9921
rs191921489	snp	A/C/G	6.59178e-05	0.00574066	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120565094	GACAGCGTCACAGAT[A/C/G]TCTCTCTCACTTGCC	9921
rs191936178	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120569854	ATCTGTGATACCGAG[A/G]TTGTGTTTTCACATA	9921
rs191943816	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF10	GRCh38.p7	12:120532820	GAATTTCTACCCAAC[C/T]ACGCCTAAACGAAAT	9921
rs191948241	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120569995	CCTCGCGGGTTCAAG[C/T]GATTCTCCTGCCCCA	9921
rs191967391	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120551532	TTGAACTCCTGACCT[C/G]AGGTGATCCGCCTAC	9921
rs191983114	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF10	GRCh38.p7	12:120533719	GCTAGAATAAGAACC[A/G]TAAATTGGCCGGGCG	9921
rs192047152	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120554134	ATGGTCTTGATCTCC[C/T]GACCTCGTGATTCAC	9921
rs192198787	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120557018	GCGTGGTGGCAGGCG[C/T]CTGTAGTCCCAGCTA	9921
rs192238144	snp	A/C	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120550942	TTAATATAAAAAAGG[A/C]AGTTATCTGACTGGA	9921
rs192333533	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577573	AAATAGTTGCAATAA[A/G]TCACCTGCACAAGCA	9921
rs192341681	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120539531	GCTGACTGGTATTCT[A/G]ACCTCTAGGCCGAGC	9921
rs192344779	snp	A/G	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120557846	GTTTGTAGAGAGTAG[A/G]TTAATTATTGGTTTC	9921
rs192426279	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120537522	AATCCCAGCTACTCG[G/T]GGGGCTGAGGCAGGA	9921
rs192462466	snp	A/G	0.00358779	0.0422022	intron-variant	RNF10	GRCh38.p7	12:120562243	TGAGAACATGTGTGC[A/G]ATATTTGGTTTTTCT	9921
rs192473581	snp	C/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120543466	CCCAGGAGTTTGAGA[C/T]CAGCCTGGGCAACAT	9921
rs192610876	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120538936	GGCTTTGAAAATTGA[A/G]GTGATTTGAAGCCTT	9921
rs192638432	snp	C/T	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120568090	TCTCTACAAAAAATA[C/T]GAAATTTAGCCAGGT	9921
rs192669805	snp	C/G	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120538731	GCTCTTGTCCCATCC[C/G]CCTGGGCCGATAGAA	9921
rs192832337	snp	A/G	4.94173e-05	0.00497053	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563864	TGCGCTGCCTCGTGC[A/G]GGAGTACGGCAGCCT	9921
rs192904421	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120548311	AAGCTGTGGAACTAA[A/G]TGAGATAGATTAAGG	9921
rs193047494	snp	C/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120544633	TGCACTCTAGCCTGG[C/G]TGACAGAGCAAAACC	9921
rs193052467	snp	G/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120571130	GGGCTCACTCATCTC[G/T]CTTGTTAAGGACACC	9921
rs193069975	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120535986	AGTTTGTACTAATCT[C/T]TGCTCTCTTTTGTAT	9921
rs193156692	snp	A/G	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120567441	GGCGTGGTGGCTTAT[A/G]CCTGTAATCCCAGCA	9921
rs193233330	snp	C/T	0.0189856	0.0955633	intron-variant	RNF10	GRCh38.p7	12:120553138	ACCCAGGCTAGAGTG[C/T]GGTGGCGTGATCTCG	9921
rs199502625	snp	A/T	1.65389e-05	0.00287562	intron-variant	RNF10	GRCh38.p7	12:120557711	ATTTTGGGGACAAAT[A/T]ATCCTGGGTACATTC	9921
rs199533622	in-del	-/TTG			intron-variant	RNF10	GRCh38.p7	12:120551293	CCCATCCTAGTGTTT[-/TTG]TTTTTTTTTTTTTTT	9921
rs199550295	snp	A/C			upstream-variant-2KB	RNF10	GRCh38.p7	12:120533129	TACAGGTGTGCAGCC[A/C]CAGCCACTATGCTTG	9921
rs199589946	in-del	-/G			intron-variant	RNF10	GRCh38.p7	12:120557097	CTCAAAAAAAAAAAA[-/G]AAAAGAAAAAAATGA	9921
rs199692114	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120545545	CTTTTATTTATTTAA[-/T]TAAATTTTTTTTTGA	9921
rs199779791	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120563125	AATGCTGTCATTGAG[C/G]TGGTAGGCATTACTG	9921
rs199793842	in-del	-/C			intron-variant	RNF10	GRCh38.p7	12:120573994	AGGTCTCCCATCCCC[-/C]AGGGAGGGCATTAAT	9921
rs199799889	in-del	-/TGT			intron-variant	RNF10	GRCh38.p7	12:120567864	ATTTCATTATGGGTG[-/TGT]GTGTGTGTGTGTGTG	9921
rs199816721	snp	C/T			upstream-variant-2KB	RNF10	GRCh38.p7	12:120534020	AAAAAAAAAAAAAAA[C/T]AACCATAAATCAAAC	9921
rs199817281	in-del	-/GG			intron-variant	RNF10	GRCh38.p7	12:120567858	AAAGCATTTCATTAT[-/GG]GGGTGTGTGTGTGTG	9921
rs199823633	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120573585	CGCCGAGTCATTTAT[A/C]AAAAAAAAAAAAAAA	9921
rs199838762	in-del	-/A	0.0788843	0.182262	intron-variant	RNF10	GRCh38.p7	12:120536464	TGACTTAAAACAAAC[-/A]AAAAAAAACAGAAAA	9921
rs199859075	in-del	-/GGGT			intron-variant	RNF10	GRCh38.p7	12:120565394	TGACCATGTTGTCCT[-/GGGT]CTACCTCTTTACAAC	9921
rs199883755	snp	C/T	9.89952e-05	0.00703476	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576699	ACCTTCTCCATCTGG[C/T]TTTTGTTTTTGTTTT	9921
rs199993342	snp	C/G/T	3.31072e-05	0.0040685	intron-variant	RNF10	GRCh38.p7	12:120552487	ATACTGATTCATTCT[C/G/T]ATTCTCTCTAGGTAG	9921
rs200013056	snp	A/C/G/T			intron-variant	RNF10	GRCh38.p7	12:120567971	ATGTATAGAAAAGAA[A/C/G/T]TGAAGGCCAGGCACG	9921
rs200067824	snp	A/C/G	4.94942e-05	0.00497444	intron-variant	RNF10	GRCh38.p7	12:120563989	GGCAGCAGTATTAAC[A/C/G]TAATCTCTTTGAGGT	9921
rs200114523	in-del	-/TTG	0.0244538	0.107838	intron-variant	RNF10	GRCh38.p7	12:120535689	TACACATAATGTCTA[-/TTG]TTGTGTGTTGGACTA	9921
rs200143363	in-del	-/TT			intron-variant	RNF10	GRCh38.p7	12:120558586	TATATATTTTTTTTT[-/TT]GAGACAGAGTCTGGC	9921
rs200160020	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120568474	GGCACATGGTTTATT[A/T]ATTTCTTTTTTTTTT	9921
rs200199431	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120561053	AGAGAATGGCTAAAA[A/C]AGCCAATTTGTTTTG	9921
rs200200679	snp	A/G	0.00013182	0.00811742	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120554723	CTATTTCTAGCTGCC[A/G]ATTTGTGGTGTCTGA	9921
rs200277775	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120568493	CTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTAGC	9921
rs200354349	snp	A/G	0.00199792	0.0315431	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120560819	AAGTAGCACTAGAGC[A/G]GCAGCTGGCAGAGGA	9921
rs200377129	snp	C/T	3.29592e-05	0.00405938	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120566913	TTCTGCTTTGGGTCC[C/T]ACCAGCACCGAGGGC	9921
rs200422237	in-del	-/AAAAA			intron-variant	RNF10	GRCh38.p7	12:120540088	CCTCATGAGGAACTT[-/AAAAA]AAAAAAAAATAGGGG	9921
rs200443491	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120572077	TTTTTTTTTTTTTTT[C/T]CTCTTCTCCAAGACG	9921
rs200471488	in-del	-/C			intron-variant	RNF10	GRCh38.p7	12:120562271	TCTTTTTCTTTCTTT[-/C]TTTTTTTTTTTTTTT	9921
rs200473562	snp	A/G	0.00127873	0.0252533	intron-variant	RNF10	GRCh38.p7	12:120563313	CGGAAAGCAGGAGAT[A/G]TCCTTTCTGTTGACT	9921
rs200520173	in-del	-/A	0.0360663	0.129354	intron-variant	RNF10	GRCh38.p7	12:120545175	GAAGAGAAAAACAAG[-/A]AACATTTTTATTTTT	9921
rs200522110	in-del	-/GTGT			intron-variant	RNF10	GRCh38.p7	12:120567861	AGCATTTCATTATGG[-/GTGT]GTGTGTGTGTGTGTG	9921
rs200541332	snp	C/T	5.01107e-05	0.00500528	intron-variant	RNF10	GRCh38.p7	12:120546392	GACGTTCTTTTGTGT[C/T]TCTTGCTTTCAGATG	9921
rs200623156	in-del	-/TTTTTTTTTT			intron-variant	RNF10	GRCh38.p7	12:120551291	GCGCCCATCCTAGTG[-/TTTTTTTTTT]TTTTTTTTTTTTGAA	9921
rs200683852	snp	C/T	9.88354e-05	0.00702908	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557593	TTGGTGATACCATTA[C/T]GATGCAGCTGATGAA	9921
rs200686697	snp	A/G	3.29495e-05	0.00405877	missense, nc-transcript-variant, intron-variant	RNF10	GRCh38.p7	12:120571247	AGTCCCTCATTCTGC[A/G]TTGGGAGTCTGGAAG	9921
rs200696006	snp	A/G	9.88663e-05	0.00703018	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576675	CAAGTGACACTACTG[A/G]CCCAGGCTACCTTCT	9921
rs200697104	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120553338	CGTGATCCACCTGCC[G/T]CGGCCTCCCAAAGTG	9921
rs200710725	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120563804	GATAGAGCCCCTTGT[C/T]CTCAGCGGAAGATGG	9921
rs200723970	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120575581	GGTCTGAAAAAGAAG[C/T]TGGACCAGCTACTTA	9921
rs200843598	in-del	-/G			intron-variant	RNF10	GRCh38.p7	12:120551295	CATCCTAGTGTTTTT[-/G]TTTTTTTTTTTTTTT	9921
rs200876147	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120555765	CCTCCCAAAGTGGTG[A/G]GATTACAGGCATGAG	9921
rs200938003	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120568475	GCACATGGTTTATTA[A/C]TTTCTTTTTTTTTTT	9921
rs201011098	snp	A/G/T			intron-variant	RNF10	GRCh38.p7	12:120549825	AATAAATAAAAATTT[A/G/T]AAAAAGGAAGTGGGC	9921
rs201135278	in-del	-/TA			intron-variant	RNF10	GRCh38.p7	12:120559944	CAGGTGATCCACCTG[-/TA]CCTCAGCCTCCCAAA	9921
rs201143861	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120567972	TGTATAGAAAAGAAT[G/T]GAAGGCCAGGCACGG	9921
rs201155461	in-del	-/C			intron-variant	RNF10	GRCh38.p7	12:120562274	TTTCTTTCTTTCTTT[-/C]TTTTTTTTTTTTTTT	9921
rs201209630	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120546625	TTTGAGAATGTCCTT[C/T]CTAGAGCATAAGCAT	9921
rs201217014	snp	C/T	8.24219e-05	0.00641905	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546534	CTTTTAACAAGATGC[C/T]TCCTCAAAGGGGCGG	9921
rs201228341	snp	A/C	0.000576525	0.0169685	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120566897	ATACCTGCTCCTCTG[A/C]TTCTGCTTTGGGTCC	9921
rs201421747	snp	G/T	1.64925e-05	0.00287158	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120566969	TCAGCAGAAGTCCAG[G/T]TTCCCATGCAGGTAA	9921
rs201430212	snp	A/G	4.95364e-05	0.00497652	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575966	GTAAGGGCAGAGGCT[A/G]GAGTGCCCAGGGTTG	9921
rs201456381	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120540855	TGCCAGTTTACTTTC[-/T]TTTTTTTTTTTTTTT	9921
rs201461855	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120573354	TTTGCCCATATCCCC[-/T]TTTTTTTTCCCTTCC	9921
rs201519227	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120572079	TTTTTTTTTTTTTCC[C/T]CTTCTCCAAGACGGA	9921
rs201559304	snp	C/G			upstream-variant-2KB	RNF10	GRCh38.p7	12:120533126	AACTACAGGTGTGCA[C/G]CCACAGCCACTATGC	9921
rs201579071	snp	A/C	0.00486471	0.0490784	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575716	CACTGGTGAAGGGGG[A/C]GTTTGGCTTCTTTCC	9921
rs201585715	snp	A/G	3.29522e-05	0.00405894	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120554733	CTGCCAATTTGTGGT[A/G]TCTGAAGACCAAGAC	9921
rs201588245	snp	A/G	4.94262e-05	0.00497098	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557429	TGGAGTAAATGTCCC[A/G]TCTGTTACAGTTCTG	9921
rs201659121	snp	G/T	0.000713616	0.0188759	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120546586	CTCTTCTTTTAATGG[G/T]GGAAGACGAGATGAG	9921
rs201672608	snp	C/T	4.94572e-05	0.00497254	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120560785	GAGCAGGTGCTGCAC[C/T]GGGTAGTTCTGGAGG	9921
rs201728776	snp	C/T	0.000181247	0.00951792	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120566847	AGTCCACATTCCCCT[C/T]GAGAATCTACAGCAG	9921
rs201785641	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120568479	ATGGTTTATTAATTT[C/T]TTTTTTTTTTTTTTG	9921
rs201909932	snp	C/T	1.65266e-05	0.00287455	intron-variant	RNF10	GRCh38.p7	12:120554670	TCTGCTGAGGGTTTA[C/T]TGGTAGATCCTGACA	9921
rs201978332	in-del	-/AAAAAAA			intron-variant	RNF10	GRCh38.p7	12:120540086	CCTCATGAGGAACTT[-/AAAAAAA]AAAAAAATAGGGGTG	9921
rs201985020	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120568480	TGGTTTATTAATTTC[-/T]TTTTTTTTTTTTTGA	9921
rs202008944	in-del	-/C/TC			intron-variant	RNF10	GRCh38.p7	12:120562270	TCTTTTTCTTTCTTT[-/C/TC]CTTTTTTTTTTTTTT	9921
rs202018576	snp	A/G	0.000399281	0.0141238	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557409	TTTCACTGAGTGAGA[A/G]GACGTGGAGTAAATG	9921
rs202051571	snp	G/T	0.185472	0.241529	intron-variant	RNF10	GRCh38.p7	12:120567866	TTCATTATGGGTGTG[G/T]GTGTGTGTGTGTGTG	9921
rs202184106	in-del	-/ATTA	0.0228947	0.104514	intron-variant	RNF10	GRCh38.p7	12:120568471	CCTGGCACATGGTTT[-/ATTA]ATTTCTTTTTTTTTT	9921
rs202213305	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120537682	CTTGAGGCAGCATTC[-/T]TTTTTTTTTGTTTAA	9921
rs202229670	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120544502	TCTCTACAAAAAACA[A/C]AAAAATCAGCTGGAC	9921
rs367607538	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120542205	TCACTCTGTAGCCCA[G/T]GGTGGAGAGCAGTGG	9921
rs367609284	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120549163	TAACAAAAGGAAGGC[C/T]TGGTGATGGAGGTGG	9921
rs367617736	snp	A/T	1.66852e-05	0.0028883	intron-variant	RNF10	GRCh38.p7	12:120560904	GAGAGGATGCATTGG[A/T]GATGCTAAACCTTTT	9921
rs367785959	snp	C/T	0.000520454	0.0161232	intron-variant	RNF10	GRCh38.p7	12:120552716	GAGTATTGCTACCCC[C/T]CAGAGGAAAGGGAAA	9921
rs367963197	snp	A/G	3.29625e-05	0.00405958	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120560790	GGTGCTGCACCGGGT[A/G]GTTCTGGAGGAGAAA	9921
rs368001408	snp	C/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120542514	ACTAACTGTTGCTAA[C/G]TGAAGTAATAGGTAA	9921
rs368033923	snp	C/T	1.64749e-05	0.00287005	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575779	CTATAGTTTTAACAC[C/T]GGTATTTTTTAGATG	9921
rs368045439	snp	A/C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576782	GAACAGATTAGCTCT[A/C/G]GGGGGAGGGGGTTTC	9921
rs368050444	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120538069	TAAAAAGATTTCTGC[A/G]GTATCTCATAAGCTG	9921
rs368063696	in-del	-/G			intron-variant	RNF10	GRCh38.p7	12:120558047	TAAAGAGTGTGATAA[-/G]TGCTCACAATGAATG	9921
rs368176272	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120569785	TCAAGTGATCCGCCT[C/G]CCTCGGCCTCCCAGT	9921
rs368183309	snp	A/G	3.29495e-05	0.00405877	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120552537	GTTTAGCCCTGCCCA[A/G]TTCTCTGGTCCTAAG	9921
rs368186683	snp	A/G	0.00398564	0.0444627	intron-variant	RNF10	GRCh38.p7	12:120536647	GCCATAGATCCCTCA[A/G]AAGATAGAAGGTAAC	9921
rs368193921	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120561393	GATTCTTGAAGCATC[A/G]CAACCACTGGTTGTT	9921
rs368226293	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120545443	GTGATCCGCCCACCT[C/T]GGCCTCCCAAAGTGC	9921
rs368266319	snp	A/G	1.89274e-05	0.00307625	intron-variant	RNF10	GRCh38.p7	12:120565555	GAACTTTCATCTTTG[A/G]CTAGCACTGCTGTAC	9921
rs368275703	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120553017	TGAGATTTAGCCTCT[C/G]CTTTATAAGGAAGAG	9921
rs368403066	in-del	-/T	0.00131154	0.0255744	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576710	TGGTTTTTGTTTTTG[-/T]TTTTTTTTTCCCCCA	9921
rs368411568	snp	C/T	1.64751e-05	0.00287007	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575719	TGGTGAAGGGGGAGT[C/T]TGGCTTCTTTCCATA	9921
rs368436753	snp	C/T	1.71384e-05	0.00292727	intron-variant	RNF10	GRCh38.p7	12:120560931	TTTTCACTTTCTCGG[C/T]GTTCTGTGGTGAAAA	9921
rs368535783	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120549845	AGGAAGTGGGCAGTG[C/G]ACCACAGGATCTAAG	9921
rs368567464	snp	A/G	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120536843	TACATTCATTAGTCA[A/G]TTGCAATAAATGCCT	9921
rs368655799	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120554012	CAGGTTCAAGTGATT[C/G]TCCTGCCTTAGCCTC	9921
rs368774808	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120553905	AATGACAGTCTTCTG[-/T]TTTTTTTTTTTTTTT	9921
rs368816127	snp	C/T	1.68732e-05	0.00290454	intron-variant	RNF10	GRCh38.p7	12:120565407	CTGGGTCTACCTCTT[C/T]ACAACCTGACCAATC	9921
rs368854890	in-del	-/TGT			intron-variant	RNF10	GRCh38.p7	12:120535693	CATAATGTCTATTGT[-/TGT]GTGTTGGACTATAGG	9921
rs368896123	snp	A/G	1.64727e-05	0.00286986	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120562999	AGGGAGGTCACTGGT[A/G]TTGTGGCTGCTCTGG	9921
rs368940837	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120563645	GTGCCGGAAGAGAGG[G/T]CTGGGTTGCCGCAGA	9921
rs368945993	snp	A/C	0.00398564	0.0444627	intron-variant	RNF10	GRCh38.p7	12:120559465	TCCCGGCTCACTGCA[A/C]TCTCCGCCTCCCAGG	9921
rs369126447	snp	A/G	1.64817e-05	0.00287064	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120566837	CAGACCCAGAAGTCC[A/G]CATTCCCCTCGAGAA	9921
rs369208983	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120540819	AATAAGTGAAGAAAT[G/T]AAGACAGCCTTCTTG	9921
rs369232522	snp	C/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120550861	TCAGCCTCCCAAAGT[C/G]CTGGGATTACAGGCA	9921
rs369265034	snp	C/T	1.64732e-05	0.0028699	intron-variant	RNF10	GRCh38.p7	12:120562936	TGGTGTTCTCTCTGG[C/T]CACGTTAGACTCGGG	9921
rs369310451	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120562638	AGTAATGGGATTGCT[C/G]GGTGAAATTTTATTT	9921
rs369538561	snp	C/T	0.000281096	0.011852	intron-variant	RNF10	GRCh38.p7	12:120571159	CCCCTTGGAACGTGA[C/T]GAATATAATCAGGTC	9921
rs369584876	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120572934	TTTAAACTAGGCTTT[A/T]TTGCTATTGCTTTTT	9921
rs369639764	snp	A/C/G	3.29853e-05	0.00406098	intron-variant	RNF10	GRCh38.p7	12:120563983	GGGTCAGGCAGCAGT[A/C/G]TTAACCTAATCTCTT	9921
rs369655335	snp	A/G	1.64925e-05	0.00287158	intron-variant	RNF10	GRCh38.p7	12:120554837	CCAAGCCCATAAGCT[A/G]TGAATGGGAGCACTA	9921
rs369715030	snp	A/G	0.000197733	0.00994119	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563476	GAACCAGAGCCTGAG[A/G]GGTTGCCAGAGGCCT	9921
rs369719020	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120538364	TGAGATTTTGTTCCA[A/G]TGGCTGGCTTAAATT	9921
rs369853121	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120555018	GATGGTGTATGAAAG[A/G]CTCTGATCTGAAGAT	9921
rs369863715	snp	C/T			intron-variant, synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120574487	TTTACTGGCCTGTGG[C/T]TGGATCTGAAAGTTA	9921
rs369880539	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120555370	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCTTGT	9921
rs369960872	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120570775	CAGGTCATAGTGTCT[A/G]CTATCGGGAATGTAA	9921
rs370024005	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120562267	TTTTTCTTTTTCTTT[C/T]TTTCTTTTTTTTTTT	9921
rs370089454	snp	A/T	0.000153988	0.00877328	intron-variant	RNF10	GRCh38.p7	12:120546395	GTTCTTTTGTGTTTC[A/T]TGCTTTCAGATGGAA	9921
rs370094183	snp	C/G/T	3.29675e-05	0.00405991	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120566953	CTCTCCATTTCTCCT[C/G/T]TCAGCAGAAGTCCAG	9921
rs370138571	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF10	GRCh38.p7	12:120533279	GCTGGTCTTGAACTC[C/T]TGGCCTCAAGTGATC	9921
rs370334473	snp	A/G	0.000153988	0.00877328	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120575663	AGCAAAAGCAGATGT[A/G]TGGCCCAAAACTGCT	9921
rs370335001	snp	C/T	4.94923e-05	0.0049743	intron-variant	RNF10	GRCh38.p7	12:120565197	GTTCTCAGGTGAGAA[C/T]GCCCCTGCTCTGCTT	9921
rs370442567	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120546985	GTCTCAAATTTTTTT[-/T]AGGAGTTTCTTAGCT	9921
rs370502396	snp	C/T	0.00398564	0.0444627	intron-variant	RNF10	GRCh38.p7	12:120552889	TGGATGTTTTTGGTA[C/T]TTAATATAATGCTTA	9921
rs370503787	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120557005	AAAAATTAGCTGAGC[G/T]TGGTGGCAGGCGCCT	9921
rs370508067	snp	C/T	0.00279162	0.0372561	intron-variant	RNF10	GRCh38.p7	12:120544977	AGGGATGCATAAAAA[C/T]GCTCACAGAGTAGTA	9921
rs370510889	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120543458	CGCCTGAGCCCAGGA[A/G]TTTGAGACCAGCCTG	9921
rs370511084	snp	A/G	0.000576782	0.0169723	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120560829	AGAGCAGCAGCTGGC[A/G]GAGGAGAAGCACACT	9921
rs370551365	snp	A/T	9.88386e-05	0.00702919	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120552557	CTGGTCCTAAGAAGA[A/T]CAACCTGAACCACTT	9921
rs370581281	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120561263	ATTCTAGAGGTGTTT[C/T]GAAAGACATTGTGGA	9921
rs370623140	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120536327	TACTTGGAAGGGTAA[A/G]GTGGGAGGATCGCTT	9921
rs370715751	snp	C/T	0.000153988	0.00877328	intron-variant	RNF10	GRCh38.p7	12:120563771	GAGCCTCCTGGGGAC[C/T]GGCCAAGACTGGTGT	9921
rs370738566	in-del	-/G	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120568648	GCCTGGCTAATTTTT[-/G]TATTTTTAATAGAGA	9921
rs370824308	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120549419	TCTGCTGCAGGGCTG[A/C]TGTGGAATAGGAAAA	9921
rs370942961	snp	A/G			intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120576079	CTTCAGCACACTCTA[A/G]TGTCATTTAAATAAT	9921
rs371038241	snp	A/C	1.64746e-05	0.00287002	intron-variant	RNF10	GRCh38.p7	12:120557530	GCCCTGCTACATATG[A/C]GTGTCCATGTTTCAG	9921
rs371145531	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120572317	GTGATCCGCCTGCCT[C/T]AGCCTCCCAAAGAGC	9921
rs371176763	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120560146	TTTTTCTGTGTGTGG[-/T]TTTTTTTGTTTTTTT	9921
rs371322841	in-del	-/AAGT			intron-variant	RNF10	GRCh38.p7	12:120536724	AAGCAATTGATAAGT[-/AAGT]TTATTTTTGTACTCT	9921
rs371355537	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120569775	ACTCATGGCTTCAAG[G/T]GATCCGCCTGCCTCG	9921
rs371457131	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120537257	GTTCGAGGTTGCAGT[A/G]AGCCACGATCACTCC	9921
rs371485318	snp	C/T	3.29457e-05	0.00405854	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120562960	ACTCGGGAAGAGGCT[C/T]TGTCGGGATTGGCCG	9921
rs371489725	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120540842	CCTTCTTGCTGAGTG[C/T]CAGTTTACTTTCTTT	9921
rs371508976	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120562257	CGATATTTGGTTTTT[C/T]TTTTTCTTTCTTTCT	9921
rs371535595	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120562503	GGTCTTGAACTTCCA[A/G]CCTCAGGTGATCCGC	9921
rs371538644	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120573575	GATTACCCGACGCCG[A/G]GTCATTTATCAAAAA	9921
rs371545443	snp	A/G	0.00438332	0.0466095	intron-variant	RNF10	GRCh38.p7	12:120553132	TCTGCCACCCAGGCT[A/G]GAGTGCGGTGGCGTG	9921
rs371560189	snp	C/T	3.29489e-05	0.00405874	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575788	TAACACTGGTATTTT[C/T]TAGATGAGAACAGCT	9921
rs371637338	snp	G/T	0.000153988	0.00877328	intron-variant	RNF10	GRCh38.p7	12:120554681	TTTATTGGTAGATCC[G/T]GACAGTCTAGCTTTT	9921
rs371674760	snp	A/G	4.11362e-05	0.00453502	intron-variant	RNF10	GRCh38.p7	12:120565571	CTAGCACTGCTGTAC[A/G]TCGTTGTATAGAACT	9921
rs371676221	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120557509	ATCCCAATCTCTTCA[C/G]TCCTTGCCCTGCTAC	9921
rs371682626	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120555808	CCTCTTTTTTTTTTT[-/T]GAGACAGTCTTGCTC	9921
rs371787819	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120544654	GAGCAAAACCTTGTC[G/T]CTAAATAAATAAAGT	9921
rs371792374	snp	C/T	0.000138447	0.0083189	intron-variant	RNF10	GRCh38.p7	12:120552714	GTGAGTATTGCTACC[C/T]CTCAGAGGAAAGGGA	9921
rs371914150	snp	A/C/G	9.88528e-05	0.00702981	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575739	TTCTTTCCATAAAAG[A/C/G]CTGTTTCTAGAAAAA	9921
rs371920910	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120574206	TTTAATGAAATCGGC[A/G]TCTGCCAACACAAAC	9921
rs372114461	snp	C/T	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120558678	GGTTTGAGCGATTCT[C/T]GTGCCTCAGCCTCCC	9921
rs372180730	snp	A/C	0.000117709	0.00767078	intron-variant	RNF10	GRCh38.p7	12:120565411	GTCTACCTCTTTACA[A/C]CCTGACCAATCTGCA	9921
rs372333043	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120545847	CCCAGCCCCCAGTAT[A/G]CTTTTAGAGCTCAAC	9921
rs372337787	snp	A/C	6.749e-05	0.00580865	intron-variant	RNF10	GRCh38.p7	12:120560922	TGCTAAACCTTTTCA[A/C]TTTCTCGGCGTTCTG	9921
rs372395039	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120555208	CTTTTTTGAGAAAGA[A/G]TCTCACTCTGTTGCC	9921
rs372408874	in-del	-/G			intron-variant	RNF10	GRCh38.p7	12:120557102	AAAAAAAAAAAAAAA[-/G]AAAAAAATGATCATA	9921
rs372428079	snp	A/G	0.000154734	0.00879448	intron-variant	RNF10	GRCh38.p7	12:120560932	TTTCACTTTCTCGGC[A/G]TTCTGTGGTGAAAAC	9921
rs372493264	snp	A/G	3.295e-05	0.00405881	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557336	CTCTATCCACCTACT[A/G]CAGCCAAGATAACCC	9921
rs372578799	snp	A/G	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120543524	TTTAAAAATTAGGTC[A/G]GGCCTGATGGCTCAC	9921
rs372583460	snp	C/T	1.6477e-05	0.00287024	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120554796	AGTTAACTGGGACTT[C/T]GTGGAACAAGTGGTG	9921
rs372686292	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120570400	CATGTTGGCCAGCCT[C/G]GTCTTGAACTCCTGA	9921
rs372688477	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120567879	TGTGTGTGTGTGTGT[A/G]TGTATGTATATATAT	9921
rs372749458	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120574284	GACAAGGCATCCCTG[C/T]TTGAACCCCATGGGG	9921
rs372869021	in-del	-/TT			intron-variant	RNF10	GRCh38.p7	12:120554260	GGCCAGGCTGGTCTC[-/TT]TAACTCCTGACCTCA	9921
rs372901479	in-del	-/TTGAA			intron-variant	RNF10	GRCh38.p7	12:120567971	ATGTATAGAAAAGAA[-/TTGAA]GGCCAGGCACGGTGG	9921
rs372957238	snp	C/T	1.64942e-05	0.00287173	intron-variant	RNF10	GRCh38.p7	12:120554842	CCCATAAGCTATGAA[C/T]GGGAGCACTAAATAA	9921
rs373069114	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120564741	TCTGTTTTTCTGCCA[A/G]CAAATAACTTTATCT	9921
rs373069215	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120548949	TGCTGGGATTACAGG[C/T]ATGAGCCACCGCGCC	9921
rs373152990	snp	C/T	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120535441	GTCCCAGATCCATTC[C/T]TCTGTCGAAGAGGAA	9921
rs373156222	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120570154	CCTCCCAAAGTGCTG[A/G]GATTACAGGCGTGAG	9921
rs373216050	snp	A/G	0.000116925	0.00764518	intron-variant	RNF10	GRCh38.p7	12:120552456	CTGCTATAAATCAGT[A/G]TCATCCTAATCTGAA	9921
rs373272492	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120537544	GAGGCAGGAGAATCC[C/G]TTGAAACCGGGAGGC	9921
rs373340814	snp	C/T	3.31038e-05	0.00406827	intron-variant	RNF10	GRCh38.p7	12:120571154	GGACACCCCTTGGAA[C/T]GTGACGAATATAATC	9921

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