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
rs373354028	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120572963	TTTCCTTTGAACTTT[A/T]TTTTGAAATACAGAG	9921
rs373432892	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120540301	ATTGAACCCGTGGGT[A/C]CTGGGCATTCATAAT	9921
rs373465055	in-del	-/C			intron-variant	RNF10	GRCh38.p7	12:120540854	GTGCCAGTTTACTTT[-/C]TTTTTTTTTTTTTTT	9921
rs373521218	snp	G/T	0.000498198	0.015775	intron-variant	RNF10	GRCh38.p7	12:120546399	TTTTGTGTTTCTTGC[G/T]TTCAGATGGAAAGAA	9921
rs373577689	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120575108	AAAAATTAGCCAGGC[G/T]GGTGCCTGTAATCCC	9921
rs373656404	snp	A/G	1.64988e-05	0.00287213	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563505	CTGTGATGACTTGGA[A/G]TTAGCAGATGACAAT	9921
rs373794206	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575740	TCTTTCCATAAAAGG[C/T]TGTTTCTAGAAAAAG	9921
rs373821449	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120541667	TCTCTATCTCCTGAC[G/T]TCGTGATCCACCTGC	9921
rs373831032	snp	A/G	6.58968e-05	0.00573969	intron-variant	RNF10	GRCh38.p7	12:120557537	TACATATGAGTGTCC[A/G]TGTTTCAGTGTTGTT	9921
rs373837828	snp	C/T	0.0023933	0.0345097	upstream-variant-2KB	RNF10	GRCh38.p7	12:120533965	TCAGCCCAGATCGCG[C/T]CACTGCACTCTAGCC	9921
rs373953144	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120546877	GTTATCACTCTTGAA[C/T]TAGAGGTACTTTTTG	9921
rs374110521	snp	A/G	3.29506e-05	0.00405884	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575757	GTTTCTAGAAAAAGA[A/G]TTGTTTCTATAGTTT	9921
rs374264680	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120541486	GTCGCCCAGACTGGA[A/G]TGCAGTGGCACGATC	9921
rs374298144	snp	A/G	3.32154e-05	0.00407512	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120565449	TTGAGAAGAGGAAAC[A/G]TCAGCGCCAAAAGAA	9921
rs374300314	snp	C/G/T	0.000216018	0.0103906	intron-variant	RNF10	GRCh38.p7	12:120552475	TCCTAATCTGAAATA[C/G/T]TGATTCATTCTCATT	9921
rs374593114	snp	A/G	0.00010266	0.00716376	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534952	GGGGCCAGCCGGCGA[A/G]TCTAAACCCAAGAGC	9921
rs374676279	snp	A/G	1.69919e-05	0.00291473	intron-variant	RNF10	GRCh38.p7	12:120552705	ACAGGCCAAGTGAGT[A/G]TTGCTACCCCTCAGA	9921
rs374761306	snp	A/G	4.96093e-05	0.00498018	intron-variant	RNF10	GRCh38.p7	12:120565226	TTCTCTTTATAGTAG[A/G]GTTCAGGGATTCTTG	9921
rs374784902	snp	A/G	4.94173e-05	0.00497053	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120562965	GGAAGAGGCTCTGTC[A/G]GGATTGGCCGGAAGC	9921
rs374793380	snp	C/T	0.000164799	0.00907592	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120566922	GGGTCCCACCAGCAC[C/T]GAGGGCCATGGGGCC	9921
rs374866107	snp	A/C/T	3.74611e-05	0.00432775	intron-variant	RNF10	GRCh38.p7	12:120565550	TTCAGGAACTTTCAT[A/C/T]TTTGACTAGCACTGC	9921
rs374875330	snp	C/T	9.90491e-05	0.00703667	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120560867	CCTGCTTTATTGAGG[C/T]AGCTATCCAGGAGCT	9921
rs375013175	snp	C/T	0.00279162	0.0372561	intron-variant	RNF10	GRCh38.p7	12:120550734	CCCGAGTAGCTGGGA[C/T]TATAGGTGCCCGCCA	9921
rs375013547	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120566273	TTTATTATGGAAATA[C/T]CAAGACAAGTAGAAC	9921
rs375098491	snp	A/G	3.29451e-05	0.00405851	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563893	CTGGAGAGGAGCCCC[A/G]AGAAGATCTCAGCAA	9921
rs375164698	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120556923	TTTGGGAGGCCGAGG[C/T]GGGCGGATCACAAGG	9921
rs375200717	snp	A/G	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120563179	AAGAGGGGACAATGA[A/G]TATTTTCTGTATGCT	9921
rs375311527	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120562275	TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT	9921
rs375315522	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120543571	CTTTGGGAGGCTGAG[A/G]CTGGTGGATCGCTTG	9921
rs375361486	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120537210	GTGAAGAGGCTGAGG[C/G]AGGGGAGGAGGAAGA	9921
rs375363253	in-del	-/A	0.0142736	0.0832652	upstream-variant-2KB	RNF10	GRCh38.p7	12:120533618	CCGTAAAGTGATATT[-/A]AATGTAAGGTATTGT	9921
rs375375600	snp	A/T	1.64735e-05	0.00286993	intron-variant	RNF10	GRCh38.p7	12:120562906	TAAGTGTGTGTCTGG[A/T]AACTTAACCTTCTCT	9921
rs375435599	snp	C/T	0.0107246	0.0724382	intron-variant	RNF10	GRCh38.p7	12:120550906	CGGCCCAGAATGCGG[C/T]GTTATTTTTAAGCTT	9921
rs375590265	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120573855	CCAGCTACTTCAGAT[C/T]CCTTCTGTGGTAAGG	9921
rs375618829	snp	A/G	6.59196e-05	0.00574068	intron-variant	RNF10	GRCh38.p7	12:120554811	TGTGGAACAAGTGGT[A/G]AGTAGCTCAGCCAAG	9921
rs375621919	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120550027	CTAGACTATAGAACA[C/G]TCCTGTCTAATAGAT	9921
rs375630450	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120568336	TGAAATGTTCAAATG[A/G]GCCTTTAGCCTTCAA	9921
rs375631535	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120536794	TGTGAATTCTCAACT[A/G]ATTTTTCTGGGGCTC	9921
rs375665129	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120552920	AATAACTTAGTATCA[C/T]GATAAGGTAGAAAAC	9921
rs375707466	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120536695	GTTGGAACTGGTTTA[A/G]AGTGGTCTGTTCAAA	9921
rs375742604	snp	C/T	0.00993419	0.0697739	intron-variant	RNF10	GRCh38.p7	12:120562530	CCGCCCACCTCAGTC[C/T]CCCAAAGTGCTGGGA	9921
rs375850249	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120576456	TGTATACCAAGACTG[A/G]TATTGGCATCTAGGC	9921
rs375902863	snp	C/G	1.64732e-05	0.0028699	missense, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575853	GAGTGATAATTCAGA[C/G]CGTGTTCCTGTGCCC	9921
rs376026028	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120549250	TAAGGTGAGCCAAGA[A/G]GAGATTTGGAAGCCT	9921
rs376044446	snp	A/G	9.8974e-05	0.007034	intron-variant	RNF10	GRCh38.p7	12:120554844	CATAAGCTATGAATG[A/G]GAGCACTAAATAAAG	9921
rs376172432	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120552409	CGTCTCAAAAAAAAA[A/G]GCTGTGTAAAAGGAG	9921
rs376181456	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120561449	CATAGGTTAAGCTCA[C/G]TAGGCTCAGTAATTT	9921
rs376213424	snp	C/T	0.000101471	0.00712217	intron-variant	RNF10	GRCh38.p7	12:120546379	ATCAGCTTCTTAAGA[C/T]GTTCTTTTGTGTTTC	9921
rs376363088	snp	A/C	0.00279162	0.0372561	intron-variant	RNF10	GRCh38.p7	12:120574117	GAGGGTCAAATGTCT[A/C]AACCGTAGGAGACCC	9921
rs376406563	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120560305	TACAGGCATGCCCTA[C/T]CAGGCCCGACTAACT	9921
rs376427405	snp	A/G/T	0.000313236	0.0125112	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546432	CCAGTGGATCCAAGC[A/G/T]TTATAATCGCAAACG	9921
rs376455543	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120575213	TGCACGCCAGCCTGG[G/T]CAACAAGAGCTAAAC	9921
rs376504606	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120551377	TTGGCTCACTGCAAC[C/T]TCTGCCTCTCGGGTT	9921
rs376525062	snp	C/T	1.67382e-05	0.00289289	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120565497	GCCGAGAGCGCAGGA[C/T]TGAGATAGAGGAGAA	9921
rs376587631	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120569538	ATTTGTGATATGCAT[C/T]TTTTTTTTTTTGAGA	9921
rs376611659	snp	G/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120559375	TTTGTGTGTGTGTGT[G/T]GTGCTTTTTTTGTTT	9921
rs376638212	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120543555	GCCTGTAATCCCAGC[A/C]CTTTGGGAGGCTGAG	9921
rs376665232	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120550692	AGCTCTGCCTCCTGG[A/T]TTCACGGCATTCTCC	9921
rs376818128	snp	C/T	1.64743e-05	0.00287	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557551	CATGTTTCAGTGTTG[C/T]TGCCACAGAGTCACA	9921
rs376837117	snp	A/C/T	0.00517822	0.0506191	intron-variant	RNF10	GRCh38.p7	12:120574335	CAGGAATAAAATGTT[A/C/T]TCTGCCTTTTAAGTG	9921
rs376891121	in-del	-/AA			intron-variant	RNF10	GRCh38.p7	12:120540091	CTTAAAAAAAAAAAA[-/AA]TAGGGGTGTGTGGGG	9921
rs377026080	snp	A/G			missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120560842	GCAGAGGAGAAGCAC[A/G]CTCCCGAGTCCTGCT	9921
rs377054423	snp	C/G/T	0.000288698	0.0120116	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534953	GGGCCAGCCGGCGAG[C/G/T]CTAAACCCAAGAGCG	9921
rs377208770	snp	C/T	1.77599e-05	0.00297987	intron-variant	RNF10	GRCh38.p7	12:120576574	AGTTAAGCTGTCTTT[C/T]TGTGTCTCCCTTTAG	9921
rs377274864	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120562263	TTGGTTTTTCTTTTT[C/T]TTTCTTTCTTTTTTT	9921
rs377281032	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120562343	GCAGTGGCGTGATCT[C/T]GGCTCATCACAACCT	9921
rs377296896	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120572018	CCTTGTAAGAAGTCC[A/G]TATAAACTTCTTTGA	9921
rs377306606	snp	A/G	6.59457e-05	0.00574182	intron-variant	RNF10	GRCh38.p7	12:120554710	TTTCCTGTCTTTCCT[A/G]TTTCTAGCTGCCAAT	9921
rs377371836	in-del	-/T/TT	0.413748	0.188909	intron-variant	RNF10	GRCh38.p7	12:120572900	CCACTGCGCCTGGCC[-/T/TT]TTTTTTTTTTTTTTT	9921
rs377456759	snp	C/T	1.64727e-05	0.00286986	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563909	AGAAGATCTCAGCAA[C/T]TGTGGTGGAGATTGC	9921
rs377565232	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120575354	CAATTTGAGGGTCTC[A/G]GTAAGAATCTCTTGT	9921
rs377595155	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120547783	TTTGAAGGACTTTGG[C/T]TTTTGTTCAGAGAGA	9921
rs377608191	snp	C/T	0.000164677	0.00907256	intron-variant	RNF10	GRCh38.p7	12:120563634	CCAAGGTGAGGGTGC[C/T]GGAAGAGAGGGCTGG	9921
rs386766979	multinucleotide-polymorphism	CA/TG			intron-variant	RNF10	GRCh38.p7	12:120572140	GGCGCGATCTTGGCT[CA/TG]CTGTAAGCTCCGCCT	9921
rs397713588	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120572076	TTTTTTTTTTTTTTT[-/T]CCTCTTCTCCAAGAC	9921
rs397790613	in-del	-/AGA	0	0	downstream-variant-500B	RNF10	GRCh38.p7	12:120578016	TCAGGCGCAATAAGA[-/AGA]GCGGAACTACAAAAA	9921
rs397849914	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120540857	GCCAGTTTACTTTCT[-/T]TTTTTTTTTTTTTTG	9921
rs397959053	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120545365	TTTTTTTTTTTTTTT[-/T]GGATTTTTAGTAGAG	9921
rs398021353	in-del	-/A	0	0	intron-variant	RNF10	GRCh38.p7	12:120575089	ACTAAAAAAAAAAAA[-/A]TCCAAAAATTAGCCA	9921
rs527449664	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120566416	CTTTTGTCTGCATCC[C/T]CTAGACCTTTGGGGG	9921
rs527576617	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120552818	AAGGGAATTGGTCTC[A/G]TTCTTTTTCTGTTCA	9921
rs527636897	snp	A/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120553271	TTATTTTTATTTTTG[A/T]TAGAGACGGGGTTTC	9921
rs527639830	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120546272	CAAAGCACTCATGCT[C/G]TGGCCCAAACCCAGA	9921
rs527829267	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120552253	TACAAAAATCAGCTG[A/G]GTGTGGTTTAATCCC	9921
rs527830597	snp	C/T			missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563849	TGCACCCTGTGAATG[C/T]GCGCTGCCTCGTGCG	9921
rs527873052	snp	A/G	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120573571	AAAAGATTACCCGAC[A/G]CCGAGTCATTTATCA	9921
rs527919958	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120541335	TTATATACCTATCCT[C/T]GTAGAATCTCCTTTG	9921
rs527920471	snp	C/T	0.000798403	0.0199641	utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534378	GGCGACTCGTCGCCA[C/T]TCCCGGAGCAGGTCG	9921
rs528060717	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120568425	AGAGTTACTATAATT[G/T]CAGAGAACTATCTTT	9921
rs528063751	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120560231	ATCTTGGCTCACTGC[A/G]ACCTCTGCCTCCTGG	9921
rs528083108	snp	G/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120567864	ATTTCATTATGGGTG[G/T]GTGTGTGTGTGTGTG	9921
rs528124001	in-del	-/T/TT	0.434398	0.168811	intron-variant	RNF10	GRCh38.p7	12:120560154	GTGTGGTTTTTTTTG[-/T/TT]TTTTTTTTTTTTTTG	9921
rs528226868	snp	A/G	0.00636936	0.0560724	intron-variant	RNF10	GRCh38.p7	12:120554066	CGTGTCACCATGCCC[A/G]GCTAATTTTTTTTGT	9921
rs528230348	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120548338	AAGGAGTGAGTGTTC[C/T]AAAAACGGATTAGGT	9921
rs528363072	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120535829	GTACTAGGTGAAGTT[C/T]TTACCTCTGTTTTCA	9921
rs528381137	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120542259	TCAACCTTGGCTTAA[A/G]CAATCCTTCCAACTC	9921
rs528382005	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120542828	AAAGTGCTGGGATTA[C/T]AGGGAGCCACCATGC	9921
rs528481464	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120575577	GGTAGGTCTGAAAAA[G/T]AAGTTGGACCAGCTA	9921
rs528498663	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120536472	AAACAAACAAAAAAA[A/C]CAGAAAATTGTAAGG	9921
rs528528148	in-del	-/A			intron-variant	RNF10	GRCh38.p7	12:120556370	AACCCCGTCTCTACT[-/A]AAAAAAAAAAATTAG	9921
rs528621978	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120569157	TATTTTTAGTAGAGA[C/T]AGGGTTTCTCCATGT	9921
rs528644493	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120576196	AAGATACAGTGGGGT[A/G]TACAACCTGTATCCT	9921
rs528686158	snp	C/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120562168	TCCACCCTCTGATAG[C/G]CCTCAGTGTGTGTTC	9921
rs528756214	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120549900	GATTTGGAGGTCCTA[A/G]TGGGGGTAAAGAATT	9921
rs528831352	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120547167	CAGATAAAAAAAATA[C/T]AGACTGAGGGAAGTA	9921
rs528953386	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120572762	CCTACCACCATGCCC[A/G]GCTAATTTTTGTATT	9921
rs528988773	snp	G/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120544386	AAATTGGCTGGGAGT[G/T]TTGGCTCATGCCTAT	9921
rs529242467	snp	C/G	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120565600	CTCTGTGTCTGGGAC[C/G]TGGGAGCCAGACCTT	9921
rs529256076	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120571884	AGCTGGGTGGGGGAA[C/T]GATAGGCTAGTGAGG	9921
rs529299888	snp	A/G	0.000148308	0.00861	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120565092	TCGACAGCGTCACAG[A/G]TATCTCTCTCACTTG	9921
rs529456254	snp	A/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120545667	CTCAGCCTCCCAAGT[A/T]TCTGGGATTATAGGT	9921
rs529552259	snp	A/C	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120540207	GCTTCAAATGATCCT[A/C]CCACCTTAGCCTCCC	9921
rs529587787	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120568625	GGATTACAGGTGTGC[A/G]TCACCATGCCTGGCT	9921
rs529671596	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF10	GRCh38.p7	12:120533057	CGTATCTCACTGCAA[C/T]CTCCAACTGCTGGGC	9921
rs529772551	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120551403	GGGTTCAAGCGATTC[A/T]CCTGCCTCAGCCTCC	9921
rs529836125	snp	C/T	0.00279162	0.0372561	intron-variant	RNF10	GRCh38.p7	12:120573811	CCTTCAGCCAAGCTA[C/T]TGAAGCAGCCTTTGT	9921
rs529860349	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120567137	AAATTCTTTTATTCA[C/T]CTTTCCCACTTGCTA	9921
rs529936139	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120554019	AAGTGATTCTCCTGC[C/T]TTAGCCTCCTAAGTA	9921
rs529985392	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120561758	CCTTGGGTAGAGTCC[G/T]GTGTATTTAACTTTT	9921
rs529997681	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120547676	GTAGTGCGTTTATTG[A/G]TTTGAGGTAAAGCAA	9921
rs530136681	snp	A/G			upstream-variant-2KB	RNF10	GRCh38.p7	12:120533569	CCGCCACGCCAGGCT[A/G]AAGAAATAAAGTGAT	9921
rs530201433	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120542131	TCAGCATCCCAAAGT[A/G]CTGGGATTACAGGCG	9921
rs530215237	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120574886	AGCCAAGATTTGCGC[C/T]ATTGCACTCCAGCCT	9921
rs530347362	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120535628	AATTAAAAACAAAAC[A/G]AATGAACTAAGGTCT	9921
rs530373402	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120568656	AATTTTTGTATTTTT[A/G]ATAGAGACAGGGTCT	9921
rs530434903	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120560994	GGTGAGATGATGGAC[A/G]CTGGGGATTAAGTTA	9921
rs530442379	snp	A/T	0.00557542	0.0525036	intron-variant	RNF10	GRCh38.p7	12:120549541	TGTAATCCCAGCACT[A/T]TGGGAGGCCAAGGAG	9921
rs530449498	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120562792	CCTGTTTCCCTCAAA[G/T]TTGAGATATTTAAGC	9921
rs530450063	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120559009	TTTAATTAATTAAAT[C/T]CATTAAAATAATTAA	9921
rs530497749	snp	A/G	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120561836	ACAGGCATAAGAAAG[A/G]CTACATAGAATTAGA	9921
rs530666086	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120571906	CTAGTGAGGCTTGCT[C/G]TGAAACCACTTTGTT	9921
rs530667752	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120555338	AGGCACCCGCCACCA[C/T]GCCTGGCTAATTTTT	9921
rs530685538	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120549645	CAAAAATTAACCGGG[C/T]GTGATGGCAGGTGCC	9921
rs530687754	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120543018	TGGAGAGAATGACAT[C/G]TCATTTATACAGTGA	9921
rs530775281	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120569538	TTTGTGATATGCATC[-/T]TTTTTTTTTTTGAGA	9921
rs530798988	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120576364	ACAACCACGTTAAAT[C/G]GGTGTACCTCACGTT	9921
rs530824582	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120537108	GAGGCTGAGGCAGGC[C/T]GATTACTTGAGCCCA	9921
rs530894010	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576858	TCCAGCTTCCTGTCT[A/T]TACACCAAAATAAAG	9921
rs530932160	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120576263	TGGAGAAGTCAGTCT[C/T]GAAGCCTGTTGCACT	9921
rs531023588	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120564039	TCACAAACCTTCAAG[G/T]CCTTTAGTTTTTGTA	9921
rs531054646	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120570330	TAGCTGGGATTACAG[G/T]TGCCCGCCACCATGC	9921
rs531084928	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120556594	AAAATGTATAAAATC[A/G]TCTGAGAATGACATA	9921
rs531295227	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120539520	AGCAGAAACTTGCTG[A/G]CTGGTATTCTGACCT	9921
rs531404080	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120571396	CTCTCATTCTAATAC[A/G]GCTGGACAAATTGAG	9921
rs531455001	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120553846	ATCTAGACTGAAGTA[A/G]CCGTTTTGTACTTTA	9921
rs531477010	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RNF10	GRCh38.p7	12:120577992	GACTTGTCTTCAGGG[C/T]GCCTTGTATTCAGGC	9921
rs531491551	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120566382	ATAGAAGGACAGTTA[C/T]TGTAAATTTGGGTTT	9921
rs531527033	snp	A/C	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120565720	CAAAGTGCCTAGCAC[A/C]TAGTAAGGATTAAGA	9921
rs531622334	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120558439	CAACTTAAAACATTA[A/G]AAATGTGTATTAATT	9921
rs531759262	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120538140	GACCTCTTGAATTAC[A/C]GAGTACTGAGTTGAG	9921
rs531812206	in-del	-/G	0.00517822	0.0506191	intron-variant	RNF10	GRCh38.p7	12:120537206	AGCTGTGAAGAGGCT[-/G]AGGCAGGGGAGGAGG	9921
rs531841176	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120546210	GAGGGGACCCGTTAG[G/T]CTTCATTATTGCAAG	9921
rs531978901	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120540331	TTTAAAAAGTCTGTG[C/T]AAGTGATTCTGGTGT	9921
rs531979286	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120546661	CTGATCCCATCCCCC[A/G]TCCCCCAGTTTATCA	9921
rs532017773	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120573536	ATTTGGATACTGTCT[C/T]AGTCCATTTGTGTGG	9921
rs532067593	snp	G/T	0.00716266	0.059414	intron-variant	RNF10	GRCh38.p7	12:120540912	CAGGCTGGAGTGTAG[G/T]GGTGCAGTCTCGGCC	9921
rs532100803	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120574067	TTAGGTCCCCACTTC[C/T]AGCATTGGGGATCAG	9921
rs532108416	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120567230	GAAAATGGAGTCTTC[C/G]CTTTGACCCACCTAT	9921
rs532222301	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120551702	TTTGCAGGTGTATCA[G/T]AGTGCACTGCAACCT	9921
rs532262102	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120553507	TCCCGGAGCTTCATG[A/C]CATTCTCCTGCCTCA	9921
rs532270720	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120567793	AGTAATTTGTAGAAC[A/G]AGAATAAATGTTCGT	9921
rs532271915	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120541535	CGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT	9921
rs532475367	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120574170	AAGTTCACCAAAGTG[A/G]AACATAATGAAGAAA	9921
rs532493776	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120535728	TGTCCTTTAACAGGG[A/G]AGGTTTTATTTCTGT	9921
rs532536658	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120574927	AGCGAAACTCCATCT[C/T]GAACAAAACAAAAAA	9921
rs532553234	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120558119	TGATTAAAATAGCAT[A/T]TCAGTCTCTGGGGAA	9921
rs532602289	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120561366	CCTGGGTCTTTTATC[C/T]TCCACAACAGAGATT	9921
rs532645060	snp	A/G	0.00029079	0.0120545	intron-variant	RNF10	GRCh38.p7	12:120560929	CCTTTTCACTTTCTC[A/G]GCGTTCTGTGGTGAA	9921
rs532687203	snp	C/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120555447	TTGGCCTCCCAAAGT[C/G]TTGGGGTTACAGGCG	9921
rs532745775	snp	G/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120549045	GAGGCAAAGTGATGT[G/T]GGGAAAAGGGAGAGA	9921
rs532892630	snp	C/T	0.00279162	0.0372561	intron-variant	RNF10	GRCh38.p7	12:120555985	TTAGAGACGGGGTTC[C/T]ACCGTGTTGTCCAGG	9921
rs532913985	snp	C/T	1.64871e-05	0.00287111	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546536	TTTAACAAGATGCCT[C/T]CTCAAAGGGGCGGCG	9921
rs532960621	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120576376	AATGGGTGTACCTCA[C/T]GTTACAGATGGGGAA	9921
rs533062061	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120549833	AAAATTTAAAAAAGG[A/C]AGTGGGCAGTGGACC	9921
rs533131910	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120549569	GAGGGTGGATCTCCT[C/G]AGGCCAGGAGTTTGA	9921
rs533198164	snp	A/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120544260	AGGCATGGTGGTTCA[A/T]GCCTTTAATCCTAAC	9921
rs533283511	snp	A/G			utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534383	CTCGTCGCCATTCCC[A/G]GAGCAGGTCGGCCTC	9921
rs533356595	in-del	-/GTTTTT	0.00136771	0.0261148	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576697	TACCTTCTCCATCTG[-/GTTTTT]GTTTTTGTTTTTGTT	9921
rs533402659	snp	C/T	1.64885e-05	0.00287123	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120565084	TAGGATGTTCGACAG[C/T]GTCACAGATATCTCT	9921
rs533454647	snp	C/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120545511	TTAAAAAGGATATGA[C/T]TCAATCTGATCCAAT	9921
rs533473090	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120551777	TGAGAGTGCAGGTGT[A/G]CATTACCGTTGCCTA	9921
rs533487959	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120561481	CATATAACAAGTTCT[A/G]GGGTGATTCTGATGG	9921
rs533495815	snp	A/G	0.00318978	0.0398085	intron-variant	RNF10	GRCh38.p7	12:120564967	ACTGTTTCCAGCCCC[A/G]GTGCTGGCTGTGTTA	9921
rs533523675	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120551011	TTATTTTTGAGACAG[C/G]GTCTTGTGGTGTCGC	9921
rs533528872	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120564702	GTTATTTATTCTGTC[A/G]GTGGTTCCCAGGTTT	9921
rs533531429	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120555654	ACCACTCCCAGCTAA[-/T]TTTTTTTTTGTATTT	9921
rs533537638	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120571497	GATTATGTCATGGAC[A/G]TCCGCTCTGTTGGAA	9921
rs533575610	snp	A/G	0.000798403	0.0199641	downstream-variant-500B	RNF10	GRCh38.p7	12:120578071	AGCTGCTACATGACC[A/G]TGCAGTAATGATGTC	9921
rs533686539	snp	C/G	3.30147e-05	0.00406279	intron-variant	RNF10	GRCh38.p7	12:120565202	CAGGTGAGAATGCCC[C/G]TGCTCTGCTTCTCTT	9921
rs533686651	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120545077	ATTAAAAGGAAAACA[C/G]TGTTAATGAGTTAGT	9921
rs533709704	snp	A/T	0.0197687	0.0974348	intron-variant	RNF10	GRCh38.p7	12:120558577	AATATGTATATATAT[A/T]TTTTTTTTTGAGACA	9921
rs533745449	snp	A/G/T	3.29545e-05	0.00405911	intron-variant	RNF10	GRCh38.p7	12:120557515	ATCTCTTCACTCCTT[A/G/T]CCCTGCTACATATGA	9921
rs533754692	snp	C/G			missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557598	GATACCATTACGATG[C/G]AGCTGATGAAGAGGG	9921
rs533826360	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120545761	CCAGGCTGGTCTCAA[A/G]CTCCTGACCTCAGGT	9921
rs533957283	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120551393	TCTGCCTCTCGGGTT[C/G]AAGCGATTCTCCTGC	9921
rs534138699	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120545376	TTTTTGGATTTTTAG[C/T]AGAGACAGGATTTCA	9921
rs534150533	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120539805	TCTTGGCAGTTGTTC[C/T]CAGTGGTGGCTGTGC	9921
rs534378181	in-del	-/A			intron-variant	RNF10	GRCh38.p7	12:120535570	AGTTTACTTACTTGT[-/A]AAGGTAGGTGGAGGT	9921
rs534401164	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120541139	TGGGATTATAGGCAT[A/G]AGCCACCGTGTCTGG	9921
rs534449269	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120539773	TTGTCCATTTTGGAA[A/T]GTGTCTTGACAGTAG	9921
rs534452743	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120547123	AGAGTAAATTACGTT[C/T]CATACCATGCAATTA	9921
rs534541920	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120559585	AGACGGGGTTTCACC[A/C]TGTTGGCCAGCATGG	9921
rs534549383	snp	A/G	0.00438332	0.0466095	intron-variant	RNF10	GRCh38.p7	12:120556989	AACCCCGTCTCTACT[A/G]AAAAATTAGCTGAGC	9921
rs534554079	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120567323	CTTTATTGTAGCATC[A/G]TTTTAATAGCTCAAA	9921
rs534610783	snp	G/T	0.00318978	0.0398085	intron-variant	RNF10	GRCh38.p7	12:120553061	TTTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT	9921
rs534668309	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120564581	AGTGAGCTGGCCTGG[C/G]CGGCAGAGCAAGACC	9921
rs534835196	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120561323	TAGGAGTACCTGAAA[C/T]GGCAAGAATTACACA	9921
rs534896460	snp	A/G	4.94947e-05	0.00497443	intron-variant	RNF10	GRCh38.p7	12:120554854	GAATGGGAGCACTAA[A/G]TAAAGGCACTGTGGT	9921
rs534963229	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577165	TAAAATGGATTTAGG[A/G]CACCCAGTTTGAATT	9921
rs535072901	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120543947	GGGGGAATAAAACAT[G/T]CTGGGCATGGTGGCT	9921
rs535136311	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120576506	CACTCTTAGCTCCCA[C/G]TCTGTGACTCTCAGT	9921
rs535146904	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120561784	CTTTTGCTTTCTTTC[C/T]ATAATACGTTGCAGC	9921
rs535187698	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120559248	GTGCAATGGTGTGAT[C/G]TCGGCTCACTGCAAC	9921
rs535306234	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120543274	GAATCTTAGAGGGTG[A/G]GGCCTGAGCATAGGA	9921
rs535406931	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120536662	AAAGATAGAAGGTAA[C/G]CAGTCCTTTTGGTCA	9921
rs535432753	snp	A/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120564476	AAATACAAAAAAAAA[A/T]TAGCTGGGTATGATG	9921
rs535556475	snp	C/T	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120545152	AGAATTGAACACATA[C/T]TATAATTGAAGAGAA	9921
rs535589273	snp	A/G			downstream-variant-500B	RNF10	GRCh38.p7	12:120577903	AAACAGATCCCAGAA[A/G]TGTCAGTAGGTAGCA	9921
rs535624740	snp	A/G	3.76067e-05	0.00433612	intron-variant	RNF10	GRCh38.p7	12:120563656	GAGGGCTGGGTTGCC[A/G]CAGAGGTGTTTCAGA	9921
rs535860983	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120550327	TCAGGGTATTGCGAG[A/G]ATAATCAGGAAGTAT	9921
rs535861037	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120556719	GGCCTTTATGCATAC[A/C]TATTAAGTTTTTTTA	9921
rs535983981	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120544736	CTAGAAAGCAACCTA[A/G]GGATGTGTAAATGGC	9921
rs535988864	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120551277	AGATGTGAGCCACTG[C/T]GCCCATCCTAGTGTT	9921
rs535993466	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120545794	TCCACCTGCCTCGGC[C/G]TTCCAAAGTGCTGGG	9921
rs536009854	snp	C/T	0.00318978	0.0398085	intron-variant	RNF10	GRCh38.p7	12:120558693	CGTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	9921
rs536011068	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120552952	TGTTTGGAATTGGAC[C/T]TAGATTTGAATCTTG	9921
rs536191769	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577183	CCCAGTTTGAATTGC[A/G]GTTTTTTTTTTTCTG	9921
rs536225102	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120573096	AGAAGTTGCAGATAT[C/T]CTGAATGATACTTTA	9921
rs536267454	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120565273	GGGGGAGGAAACTTA[C/T]GGAACTGTATCATGA	9921
rs536276459	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120572211	AGCTGGGACTATAGG[C/T]GCCTGCCACCACGCC	9921
rs536319832	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120552355	CAGTGAGCCAAGATC[A/G]TGCCATTGCACTCCA	9921
rs536357022	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120550721	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	9921
rs536388702	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120573611	AAAAAGTTTATTTGG[C/T]TCATGACTCTGCTGG	9921
rs536444624	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120575194	TGAGCCAATATTGTG[C/G]CATTGCACGCCAGCC	9921
rs536614338	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120541055	AGAGACGGGGTTTCT[C/G]CATGTTGGTCAGGCT	9921
rs536709766	in-del	-/TTAAT	0.00636936	0.0560724	intron-variant	RNF10	GRCh38.p7	12:120559027	TTAAAATAATTAAAA[-/TTAAT]TTAATTAATTAAATT	9921
rs536753633	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534463	ACCGAGACAGCCAGC[C/T]CTCTCCCCTGCCTCG	9921
rs536784024	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120541769	CTCTCGCTCTGTCAC[C/T]TAGGCTGGCATGCAG	9921
rs536872358	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120568528	TCACCCAGGCTGGAG[G/T]GCACTGGTGCAATCT	9921
rs536909121	snp	A/G			upstream-variant-2KB	RNF10	GRCh38.p7	12:120532483	GCTTGTCTCATAGGT[A/G]AGAACATCACTTGTT	9921
rs536972813	snp	A/G	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120553646	CTGACTTCATGATCC[A/G]CCCGCCTCGGCCTCC	9921
rs536979143	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120566201	TAGGTGTTTGGCACA[C/T]GTCCTGAACTTTGAG	9921
rs537001198	snp	A/G	0.00557542	0.0525036	intron-variant	RNF10	GRCh38.p7	12:120560472	TTGAGCTTTTCTGAT[A/G]TTACATACAATGCTG	9921
rs537018663	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120547921	GTGAGAGTGATGGAA[A/G]CTTTGAAAGAGGGTG	9921
rs537055475	snp	C/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120554156	GTGATTCACCTGCCT[C/T]GGCCTCCCAAAGTGC	9921
rs537137726	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120556090	CACCACGCCCAGCTT[C/T]AGTTGCACTTTCAAA	9921
rs537155673	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120572546	AACTGCTGGACTTAG[A/G]GATGATTAACAAGTG	9921
rs537221819	snp	C/G	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120569217	CAGGTGATCCGCCAG[C/G]TGACCTCAGGTAATC	9921
rs537223842	snp	A/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120574986	GGCTCACGCCTATAA[A/T]CCCAGCACTTTGGGA	9921
rs537311859	snp	C/T	0.00318978	0.0398085	intron-variant	RNF10	GRCh38.p7	12:120540824	GTGAAGAAATGAAGA[C/T]AGCCTTCTTGCTGAG	9921
rs537385311	snp	C/T	1.6473e-05	0.00286988	missense, utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120575668	AAGCAGATGTGTGGC[C/T]CAAAACTGCTCCAAA	9921
rs537406545	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120537765	TGGCTTCTGCTGTGC[C/G]TGTTCGTTTAGCAAG	9921
rs537424633	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577247	AGTAGGCTGTCCTTG[A/G]CACTTGCATGTGTGA	9921
rs537443832	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120569252	TGCCTTGGCCTCCCA[A/G]AGTCCTGGGATTACA	9921
rs537588077	snp	C/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120570863	AGTCCCTGACAGTAC[C/G]TATCCTTGAGAGCCA	9921
rs537641467	in-del	-/AT	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120556607	TCATCTGAGAATGAC[-/AT]AGCATAAAAACTTAA	9921
rs537779170	snp	A/C/G	0.000115312	0.00759235	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557402	CACTATCTTTCACTG[A/C/G]GTGAGAAGACGTGGA	9921
rs538090592	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF10	GRCh38.p7	12:120532496	GTAAGAACATCACTT[A/G]TTAGCTATGTGATAA	9921
rs538168035	snp	A/G	0.0023933	0.0345097	intron-variant	RNF10	GRCh38.p7	12:120550810	ACTGTGTTAGCCAGG[A/G]TGGTCTCGATCTCCT	9921
rs538223617	snp	C/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120559493	AGGTTCAAGAGATTC[C/T]CCTGCCTCAGCGTCC	9921
rs538274782	in-del	-/GTAGCT	0.00122224	0.0246907	intron-variant	RNF10	GRCh38.p7	12:120570020	GCCCCAGCCTCCTGA[-/GTAGCT]GTGTAGCGTGCCACC	9921
rs538337097	snp	C/G	1.64925e-05	0.00287158	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546430	CTCCAGTGGATCCAA[C/G]CGTTATAATCGCAAA	9921
rs538342448	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120539772	CTTGTCCATTTTGGA[A/G]TGTGTCTTGACAGTA	9921
rs538400087	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120547047	TACAAGGGTATTCAC[C/T]GCTTTGTTTGTAGTT	9921
rs538418050	snp	A/G	0.00795532	0.062565	intron-variant	RNF10	GRCh38.p7	12:120572257	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTATT	9921
rs538418462	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120540574	CTGATGGTACCTTCA[A/G]CCTTTAGCTGCCTTT	9921
rs538509257	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120555551	GGAGTACAGTGGTGC[A/G]ATCTTGGCTCACTGC	9921
rs538555719	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120541113	CCGCCCGCCTCGGCC[C/T]CCCAAAGCATTGGGA	9921
rs538577395	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120572876	AAAGTGCTGGGATTA[C/T]AGACATGAACCACTG	9921
rs538626281	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120567511	ttcaagaccagcctg[A/G]ccaacacagtgaaac	9921
rs538631496	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120558807	AACTCCCGAGCTCAA[C/G]TGATCTGCCCGCCTT	9921
rs538700922	in-del	-/CAC	0.0107246	0.0724382	intron-variant	RNF10	GRCh38.p7	12:120567822	TGGGTTTTAAAAAAA[-/CAC]CACCACCACCACCAC	9921
rs538816380	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120561087	TTTGTTTGATGACAG[C/T]AGAGAAGGTTTAACC	9921
rs538825821	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120554215	TGGCCTAATTTTTCT[A/G]TTTTTAGTAGAGATG	9921
rs538838733	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120553110	TTTTTTTGAGATGTA[G/T]TCTCGCTCTGCCACC	9921
rs538887414	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120553649	ACTTCATGATCCACC[C/T]GCCTCGGCCTCCCAA	9921
rs538999837	snp	A/C	0.000557258	0.0166829	intron-variant, splice-acceptor-variant	RNF10	GRCh38.p7	12:120574466	TTTTATTGTCCTTGC[A/C]GGAATTTTACTGGCC	9921
rs539058807	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120535393	TGAGGGCCCAAGGAC[C/G]TTTCAAACTCAGATC	9921
rs539122677	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120575128	CCTGTAATCCCAGCT[A/C]CTTGGGAGGCTGAGA	9921
rs539165928	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120554665	CAATTTCTGCTGAGG[A/G]TTTATTGGTAGATCC	9921
rs539166338	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120539068	GAACGCTTTGGATTT[A/T]TTAATGATAGGCTTT	9921
rs539302669	in-del	-/TCT			cds-indel, nc-transcript-variant	RNF10	GRCh38.p7	12:120577278	AAGGAGGGTTTTGCC[-/TCT]TCTTGAGCATGGCTT	9921
rs539392672	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120569818	GCTGGGATTATAGGC[C/T]TGAGCCACTGTGCCC	9921
rs539548392	snp	A/G	0.00358779	0.0422022	intron-variant	RNF10	GRCh38.p7	12:120535976	TTTATTTCGAAGTTT[A/G]TACTAATCTCTGCTC	9921
rs539613456	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120537348	AAAACTCATGTAGGC[C/T]GGGTGCGGTGGCTCA	9921
rs539615989	snp	A/G	0.00398564	0.0444627	intron-variant	RNF10	GRCh38.p7	12:120544646	GGGTGACAGAGCAAA[A/G]CCTTGTCTCTAAATA	9921
rs539750919	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120537941	GCTGCCTTAGGAACG[C/T]AACAGCTAAGACCAG	9921
rs539790463	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120562645	GGATTGCTGGGTGAA[A/G]TTTTATTTCTGTCTT	9921
rs539810318	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120556194	AAGAATAATAATTTC[A/G]AAATGATGGGCACTT	9921
rs539846492	snp	C/T	6.73934e-05	0.00580449	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563361	GGGTGTGCTGGAGTA[C/T]CTGTCTGCCTTCGAT	9921
rs539860388	snp	C/T	6.58903e-05	0.00573941	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563859	GAATGTGCGCTGCCT[C/T]GTGCGGGAGTACGGC	9921
rs539904083	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120544121	AATCCTAGCTACTTG[A/G]GAGGCCAAGGCAGGA	9921
rs540287598	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120553426	TTTTTTTTTTGAGAC[A/C]AAGTCTTGCTCTGTC	9921
rs540329411	snp	C/T	1.90395e-05	0.00308535	intron-variant	RNF10	GRCh38.p7	12:120565556	AACTTTCATCTTTGA[C/T]TAGCACTGCTGTACG	9921
rs540491572	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	RNF10	GRCh38.p7	12:120577764	AAGAAATCCTATCAG[A/G]AAATTTCCTGGATGG	9921
rs540513253	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120539162	AATCCTCATGATTCT[A/C]TGAGGAAGTATGGTA	9921
rs540576552	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120538296	CCTTTGGTTTCTATT[C/G]TGTAAACTGTCATTA	9921
rs540624655	snp	A/G	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120540024	ATTTTTAGTAGAGAT[A/G]GGTTTCGCCATGTTG	9921
rs540770582	snp	A/T	0	0	upstream-variant-2KB	RNF10	GRCh38.p7	12:120532980	TCTGTTTCTACTTTT[A/T]AAAAAAAAGTTTAGA	9921
rs540803470	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120537337	AAACTTCTGTAAAAA[C/T]TCATGTAGGCCGGGT	9921
rs540891308	in-del	-/C			upstream-variant-2KB	RNF10	GRCh38.p7	12:120534260	ACAAAAACCAAAAAA[-/C]AAACCACGAGACCCG	9921
rs540901186	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120573369	CTTTTTTTTCCCTTC[C/T]ATGGCCAGTTGTTTT	9921
rs540966828	in-del	-/AT	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120557740	CTTTAAGGTGATTGA[-/AT]ATATATCTAAGCATC	9921
rs541175646	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120554341	CCACTGTGCCTGGCC[A/G]AGAACAGTCTTTTCA	9921
rs541279958	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120574881	CGGTAAGCCAAGATT[C/T]GCGCCATTGCACTCC	9921
rs541536016	snp	C/T			upstream-variant-2KB	RNF10	GRCh38.p7	12:120534078	TCCAATGTTTGGCTA[C/T]ATTATTATCAGTGTA	9921
rs541605529	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120564189	TGTAGTTTGGGGATA[C/T]AGATATTTCTTTTAT	9921
rs541623584	snp	G/T	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120548105	ATTCTTTCAAGAAGA[G/T]CACAAAGTTTTTTTG	9921
rs541680716	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120562844	TCTCATTGCCTTTTA[A/G]CTTTTGGTCCTGTTG	9921
rs541725347	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120536108	AGGTCCAGTTTAAAA[C/T]TTGTCAAGATTAAAA	9921
rs541806504	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120568936	CAAGAAAGATACTTT[C/T]TGATGCTTACGTCTG	9921
rs541869967	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120561759	CTTGGGTAGAGTCCT[A/G]TGTATTTAACTTTTG	9921
rs542003760	in-del	-/TTGTT	0.00518648	0.0506591	intron-variant	RNF10	GRCh38.p7	12:120572591	TGCCAAATACTTGTT[-/TTGTT]TTGTTTTGTTTTGTT	9921
rs542198484	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120564787	CTCAGCTGTGGGGCC[C/T]TGAAAAAATCAGAAA	9921
rs542232222	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120543523	ATTTAAAAATTAGGT[C/T]GGGCCTGATGGCTCA	9921
rs542237744	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120576217	CCTGTATCCTTTAGA[A/G]TCTTGAGTTGGTACA	9921
rs542387912	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120564021	GGCCTAGCCATCCTA[A/G]GTTCACAAACCTTCA	9921
rs542409133	snp	C/T	0.00159617	0.0282053	intron-variant, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120539426	TGTAGTAAGGCCATA[C/T]GTTGCCCCTCTGGAG	9921
rs542437934	in-del	-/A	0.00285367	0.0376655	intron-variant	RNF10	GRCh38.p7	12:120566801	TCTGTAAATGGGTTT[-/A]CAAGGGTTATCTTTC	9921
rs542465048	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120571982	TAAGTGAGGAAGATG[G/T]ATGGACAGCTTGACA	9921
rs542675489	in-del	-/A	0.483126	0.0902898	intron-variant	RNF10	GRCh38.p7	12:120557085	GAGATGGACCGTCTC[-/A]AAAAAAAAAAAAAAA	9921
rs542693375	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120538544	GCTTCATTCCAGTAG[C/T]GTTAATAGGTATTTC	9921
rs542791848	snp	A/G	0.00557542	0.0525036	intron-variant	RNF10	GRCh38.p7	12:120559095	AAAAATTAACTGGGC[A/G]TGCAGGTATAGTTAA	9921
rs542885351	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RNF10	GRCh38.p7	12:120532783	GCACAGTAGACCAAA[C/T]CAAAACAGAGTTACT	9921
rs542946503	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120539896	GCTGGAGTTCAGTGG[C/T]GCGATCTCAGCTCAC	9921
rs542953676	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120543294	TGAGCATAGGAATTC[C/T]GTAAAAGCTCATCTG	9921
rs542979603	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120541873	TGGTTTATCTTTTTC[-/T]TTTTTTTTTTTGAGA	9921
rs543020253	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120565682	AATAGGCTTGCTTGC[A/C]AATATAATGAGTTAA	9921
rs543209197	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120559632	TTGTGATCCGCCTAC[C/G]TCAGCCTCCCAAAGT	9921
rs543229174	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120560191	AGTTTCGCTTTTGTT[C/G]CCCAAGCTGGAATGC	9921
rs543245228	snp	A/G	3.71609e-05	0.00431034	intron-variant	RNF10	GRCh38.p7	12:120552746	AGTAGGACTCTCCGG[A/G]TAGCTGTGGTGCCTC	9921
rs543369122	snp	C/G	3.37633e-05	0.00410859	intron-variant	RNF10	GRCh38.p7	12:120546613	TGAGGTATGGAATTT[C/G]AGAATGTCCTTTCTA	9921
rs543376985	snp	A/G	0.00318978	0.0398085	intron-variant	RNF10	GRCh38.p7	12:120548226	TAAGTAGAGGTAGGT[A/G]GTTAACTGTGAATCA	9921
rs543417359	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120555078	CCTCCTGATCTGGGT[C/T]GGGCTCATTACAGGG	9921
rs543516224	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120535026	GCTGCTGGGGAGAGT[C/T]GTTGCTCTCATCGGC	9921
rs543536087	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120548690	TTGAGATGGAGTCTC[A/G]CTCTGTCCCCCCAGG	9921
rs543660414	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120576012	ATGTACTGCCATTCC[C/T]GCCTGGATTCAGTGG	9921
rs543662875	in-del	-/A	0.4941	0.0539917	intron-variant	RNF10	GRCh38.p7	12:120566762	GTGAGACCCCATCTC[-/A]AAAAAAAAAAAAAAA	9921
rs543664414	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120569035	GAGTGCAATAGTGCA[A/G]TCTCAGCTTACTGCA	9921
rs543800765	snp	A/C	0.00636936	0.0560724	intron-variant	RNF10	GRCh38.p7	12:120554441	TGATGGAGTCACGGT[A/C]TAGGTTAATTTTAGT	9921
rs543822200	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120569608	ACAAGGCACAATCTC[A/G]GCTCACTGCAACCTC	9921
rs543946083	snp	C/T	1.66034e-05	0.00288122	intron-variant	RNF10	GRCh38.p7	12:120563763	GGGGTGGGGAGCCTC[C/T]TGGGGACTGGCCAAG	9921
rs543967804	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120536338	GTAAGGTGGGAGGAT[C/T]GCTTAAGCTCAAGGA	9921
rs544081011	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB	RNF10	GRCh38.p7	12:120533975	TCGCGCCACTGCACT[C/G]TAGCCTGGGCGACAG	9921
rs544176976	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120562889	GCCCTTGCCCTTCAA[A/G]CTAAGTGTGTGTCTG	9921
rs544226519	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120551104	TATCCTCCCACCTCA[C/G]CCTTCCAAGTAGATG	9921
rs544347950	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120573366	CCCCTTTTTTTTCCC[-/T]TCCATGGCCAGTTGT	9921
rs544422582	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120549763	GCACTCCAGCTTGGG[C/T]GACAGAGCAAGACTC	9921
rs544480715	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120537602	CATTGCACTCCAGCC[C/T]GTCTAAAAAAACAAA	9921
rs544503489	snp	G/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120544777	ATATTTTATCTGTCA[G/T]TTCCACTTTTTGAGA	9921
rs544564979	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120544228	TGAGACTGTTAAAAA[C/T]AAAAAAAAGATAAAC	9921
rs544591355	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120538068	ATAAAAAGATTTCTG[C/T]AGTATCTCATAAGCT	9921
rs544671393	snp	A/G	0.00318978	0.0398085	intron-variant	RNF10	GRCh38.p7	12:120571059	GTTGAAAGTTGGATC[A/G]ATGTTTGCTTTTTTT	9921
rs544682584	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120551667	CTCACCCTGTTGCCC[A/G]GGCTGGAGTGCAGTG	9921
rs544686313	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120539976	GAGTAGCTGGATTGC[A/G]GGTGTCCACCACCAC	9921
rs544745659	snp	A/G	0.0023933	0.0345097	intron-variant	RNF10	GRCh38.p7	12:120545472	GCTAGGATTACAGGC[A/G]TGAGCCACCGCGCCT	9921
rs544773248	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120557020	GTGGTGGCAGGCGCC[C/T]GTAGTCCCAGCTACT	9921
rs544834537	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120564899	GCTTATTCCACCTTG[C/T]TGTAGGTTGACAGTT	9921
rs544858486	snp	G/T	0.0111196	0.0737302	intron-variant	RNF10	GRCh38.p7	12:120555511	TTTTTTTTTGAGACG[G/T]AGTTTCGCTCTTGTT	9921
rs544873646	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120572652	CAAGGCTGGAGTGCA[A/G]TGGCGTGATCTCGGC	9921
rs545017638	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120571799	TTACATAAAATGAGC[C/T]ATTTCTCTTCACTTT	9921
rs545022509	in-del	-/AGTT	0.000398618	0.0141121	intron-variant	RNF10	GRCh38.p7	12:120567014	ATGAATTCACCCATC[-/AGTT]AGACCTTATGCAAAG	9921
rs545248169	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120573235	GCATATTTATATCTC[C/T]ACATTTGTCTCAGCG	9921
rs545295371	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF10	GRCh38.p7	12:120533875	AGCCGGGCGTGGTGG[C/T]GGGCGCCTGTGGTCC	9921
rs545381415	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120549270	TTTGGAAGCCTGAGG[A/G]GTGAAGGAGTTGTCT	9921
rs545461570	snp	A/T			upstream-variant-2KB	RNF10	GRCh38.p7	12:120533382	TTTTAAAAAATATTT[A/T]TATTCTTTAGAGACA	9921
rs545550903	snp	A/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120547474	TTTTTCTTTTTCTTT[A/T]TTAGAGAGTGGATCT	9921
rs545697530	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120535081	CTTTCTTTTATAGCT[C/G]CTACCTGCCCTTTTC	9921
rs545699180	snp	C/T	0.00716266	0.059414	intron-variant	RNF10	GRCh38.p7	12:120541927	GCTGGAGTGCAGTGG[C/T]GCAATCTTGGCTCAC	9921
rs545760861	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120541299	GTCTTGGATAATGAG[A/G]TTGGAGGATATGTGT	9921
rs545781814	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120574804	GGTGGTGCATGCCTA[G/T]AATCCCAGCTACTCA	9921
rs545787397	snp	C/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120535562	GTGCCCCGAGTTTAC[C/T]TACTTGTAAAGGTAG	9921
rs545872760	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120568370	GTTTGTCTTATATAT[A/G]AAGAATGTTTAAAGT	9921
rs545875246	snp	C/T	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120536820	GGCTCCTCTTTAAGC[C/T]ACTAACATACATTCA	9921
rs546124406	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120555210	TTTTTGAGAAAGAGT[C/G]TCACTCTGTTGCCCA	9921
rs546126873	in-del	-/A	0.340402	0.233083	intron-variant	RNF10	GRCh38.p7	12:120575077	ACCCCGTCTCTACTA[-/A]AAAAAAAAAAAATCC	9921
rs546138239	snp	C/T	0.00676609	0.0577691	intron-variant	RNF10	GRCh38.p7	12:120569985	GCAACTTCCCCCTCG[C/T]GGGTTCAAGCGATTC	9921
rs546407439	snp	A/G	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120543823	ATTTAAAAATTAGCT[A/G]GGTGTGGTGGTGCAC	9921
rs546547148	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120536985	AGTGGAATTAACTCT[A/G]ATTACCCAACAAGAT	9921
rs546567378	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120543215	AAAAATTACTCAGAT[A/G]ATATTACAGGTCTGC	9921
rs546585678	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577008	CATTAGAGCAGTCCA[A/T]CCCAGAATGGCACAC	9921
rs546598102	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120549120	GGAGCAGTTGTCTTA[C/G]ATAGGAACTCTACCA	9921
rs546644105	snp	A/C/G	0.000543478	0.0164757	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120557594	TGGTGATACCATTAC[A/C/G]ATGCAGCTGATGAAG	9921
rs546657710	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120568610	CCTCATGAGTAGCTG[C/G]GATTACAGGTGTGCG	9921
rs546671339	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120556518	CCTGGGTGACAGAGT[A/G]AGACTCCGTCTCAAA	9921
rs546770679	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120537721	TTAGAAAGCTTGACC[A/G]TGTTTGCCACCGCCA	9921
rs546799358	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120574040	CCACCCCCATGACCC[A/G]TACATCTCCCATTAG	9921
rs546819983	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120576389	CACGTTACAGATGGG[A/G]AAACTGAGGTCCAGG	9921
rs546833806	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120537163	AAAAATAAATGAGCC[A/G]GGCGTGGTGGCACGC	9921
rs546851346	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120546091	CATTTCCTGTAACTT[C/T]ATCTGACTGAACTTT	9921
rs546867778	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120545105	AGTGCTCTGTGGGTA[C/T]TGGCAACTTTAAATT	9921
rs546883417	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120569851	CCTATCTGTGATACC[A/G]AGATTGTGTTTTCAC	9921
rs546915286	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120538820	GTATGAAGCACTGCC[C/G]TGGCATTCTTCCTGT	9921
rs546939827	snp	A/C/G	0.00398691	0.0444912	upstream-variant-2KB	RNF10	GRCh38.p7	12:120532339	GGTCAGGCTGGTCTC[A/C/G]ATCTCCTGACCTGTT	9921
rs546997642	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120559361	TAATTTTTGTTTTTT[G/T]TGTGTGTGTGTGTTG	9921
rs547001614	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120554523	TTCATGGATTTAGAC[C/T]TCTGCCTGCTGAGTC	9921
rs547014136	snp	G/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120556689	TACTGGTAGATTACT[G/T]CTAGACCCTTTTTAG	9921
rs547016329	snp	A/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120564987	TGGCTGTGTTATGTA[A/T]ATATTGTTGGATATC	9921
rs547021809	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577211	CTGACACATGGCCAG[A/G]CTGTGGTGCCAGCTT	9921
rs547051159	snp	A/C	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120564473	AAAAAATACAAAAAA[A/C]AATTAGCTGGGTATG	9921
rs547077677	in-del	-/AG	0.00557542	0.0525036	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577139	CCTTGTTAAAGAAAC[-/AG]GGGTGGGAATAAAAT	9921
rs547079038	snp	C/T			utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534621	GGTCGCCGCTGCCGC[C/T]GGGCTTAACAGCCCC	9921
rs547180740	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120548959	ACAGGCATGAGCCAC[C/T]GCGCCCGGCTGAGGG	9921
rs547251409	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120552854	GCCCCGCCCTTCCTT[C/T]CTTTTACCCACTTTC	9921
rs547299745	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120545522	ATGACTCAATCTGAT[C/T]CAATATGCTTTTATT	9921
rs547411809	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120553294	GGGGTTTCACCATAT[C/T]GGCCAGGCTGGTCTC	9921
rs547463177	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120540472	CACTCCTGTTCTACC[C/T]TCGAGTTTTTCCCAT	9921
rs547498549	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120546346	TGGGAGGTGGAGGGC[A/C]GTTGGCTAAGTGAAT	9921
rs547576000	snp	A/T	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120574314	GTTTGTCTCTTGATA[A/T]TTTTCCAGGAATAAA	9921
rs547703411	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120561070	GCCAATTTGTTTTGG[G/T]CTTTGTTTGATGACA	9921
rs547703599	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120573572	AAAGATTACCCGACG[C/G]CGAGTCATTTATCAA	9921
rs547771155	in-del	-/A	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120537473	CTCTACTAAAAGTAC[-/A]AAAAATTAGTCCGGC	9921
rs547777707	in-del	-/TTGTT	0.0020012	0.0315689	intron-variant	RNF10	GRCh38.p7	12:120572595	AATACTTGTTTTGTT[-/TTGTT]TTGTTTTGTTTTGTT	9921
rs547964044	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120535258	GCTAGTATTTGGCTC[A/C]CAGCAGGCCTTAAGA	9921
rs548018614	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120547881	GTGGAAGCAGGAAGA[C/T]TAAGAGACTACAAAG	9921
rs548026363	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534396	CCGGAGCAGGTCGGC[C/T]TCGGCCCAGGGGCGA	9921
rs548038993	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120535679	TTGCGCCAAATACAC[A/G]TAATGTCTATTGTTG	9921
rs548094411	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120536053	GCGACAGTGGGGATG[G/T]TGTGGCAGAGAGGGA	9921
rs548101834	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120554119	ACCGTGTTAGCCAGG[A/G]TGGTCTTGATCTCCT	9921
rs548185272	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120554095	GTATTTTTAGTAGAA[C/T]GGGGTTTCACCGTGT	9921
rs548305098	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120536523	TCACCTGCTGGATAT[A/G]GCAAACTTGTTTACC	9921
rs548333200	in-del	-/TTG	0.000346332	0.0131547	cds-indel, nc-transcript-variant	RNF10	GRCh38.p7	12:120576702	TTCTCCATCTGGTTT[-/TTG]TTTTTGTTTTTTTTT	9921
rs548344803	snp	A/G	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120569719	ATTTTTGTATTTTTA[A/G]TAGAGATGGGGTTTC	9921
rs548354093	snp	C/G	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120542260	CAACCTTGGCTTAAG[C/G]AATCCTTCCAACTCA	9921
rs548472702	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120574977	GGGCACAGTGGCTCA[C/G]GCCTATAATCCCAGC	9921
rs548490902	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120535834	AGGTGAAGTTTTTAC[C/G]TCTGTTTTCACTGTG	9921
rs548509857	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120549926	GAATTGTTGGAGTCA[C/G]GACTAAACCTGGGGA	9921
rs548551393	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120569211	TGACCTCAGGTGATC[C/T]GCCAGCTGACCTCAG	9921
rs548638150	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120538326	AATGGCCATTTGCTT[C/T]CTAGCTACATGATTA	9921
rs548664180	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120544552	GTCTCAGCTGCTCAG[A/G]AGGCTGAAGTGGGAG	9921
rs548728214	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120565934	GAAATTTTGATAGAC[C/T]AGGAAATGCAGGAAG	9921
rs548754713	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120571369	ATGGGAACCTCCTCC[A/G]GGGATTGTTACCTCT	9921
rs548796451	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	RNF10	GRCh38.p7	12:120577887	CATTGTATTATGGAG[A/C]AAACAGATCCCAGAA	9921
rs548796482	snp	A/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120570779	TCATAGTGTCTACTA[A/T]CGGGAATGTAAAAGC	9921
rs548827574	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120556928	GAGGCCGAGGCGGGC[A/G]GATCACAAGGTCAGG	9921
rs548946857	snp	C/G			missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120560782	AAGGAGCAGGTGCTG[C/G]ACCGGGTAGTTCTGG	9921
rs549153717	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120564477	AATACAAAAAAAAAT[C/T]AGCTGGGTATGATGA	9921
rs549269021	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120544624	TTGTGCCACTGCACT[C/G]TAGCCTGGGTGACAG	9921
rs549269971	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120539629	TAATTTGGTAATGGG[A/G]GGAGGCTGAGATATA	9921
rs549335877	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120558250	GATAGATTGAAGAAG[G/T]AAATGTAAAAAATCC	9921
rs549375744	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120551334	GAGTTTTGCTCTTGA[C/T]GCCAGGCTGGAGTGC	9921
rs549461386	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RNF10	GRCh38.p7	12:120532488	TCTCATAGGTAAGAA[A/C]ATCACTTGTTAGCTA	9921
rs549533530	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120545211	TTTGAGACGGAGTCT[C/T]GCCCTGTCACCCAGG	9921
rs549544550	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120553340	TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT	9921
rs549567593	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120559428	TCTCACTCTGTTGCC[A/C]GGCTGGAATGCAGTG	9921
rs549621390	snp	A/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120545690	TTATAGGTGCCCGCC[A/T]CCATGCGCGGCTAAT	9921
rs549664478	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120572224	GGCGCCTGCCACCAC[A/G]CCCGGCTAATTTTTT	9921
rs549699571	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120540294	AGCCTAGATTGAACC[C/T]GTGGGTCCTGGGCAT	9921
rs549706011	snp	A/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120546985	GTCTCAAATTTTTTT[A/T]AGGAGTTTCTTAGCT	9921
rs549724562	snp	A/G	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120541521	CTCACTGCTAGCCCC[A/G]CCTCCCGGGTTCACG	9921
rs549766596	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120547701	AAGCAAGTAGGCTAC[C/T]GTAAGTGGAGGAGGA	9921
rs549828818	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120572819	TTGGCCAGGCTGGTC[C/T]AGAACTCTTGACCTC	9921
rs549846392	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120554023	GATTCTCCTGCCTTA[C/G]CCTCCTAAGTAGCTG	9921
rs549859223	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120567177	CTTTACCCTGCCAGC[G/T]TCTAAGCACCTCAAG	9921
rs549864764	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534467	AGACAGCCAGCCCTC[C/T]CCCCTGCCTCGCGGC	9921
rs549988898	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120574890	AAGATTTGCGCCATT[A/G]CACTCCAGCCTGGGC	9921
rs549990691	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120567986	TTGAAGGCCAGGCAC[A/G]GTGGCTCACACCTGT	9921
rs550086256	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120565634	CACTTGTTTTCTTCA[A/G]CTTTTAAATGTGAAT	9921
rs550287312	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120559284	CCTCCTCGGTTCAAA[C/T]GATTTTCCTTCCTCA	9921
rs550404453	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120561024	AGTTCCATTCCACAT[C/T]TAAGACAATAAGCAG	9921
rs550474610	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120538574	CTGAGAACATGCAGC[A/C/G]GTAAATATCCTGTGA	9921
rs550608120	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120576466	GACTGGTATTGGCAT[C/T]TAGGCAGTCTAATTC	9921
rs550639737	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120540563	GGGTCCCAGGCCTGA[C/T]GGTACCTTCAACCTT	9921
rs550754170	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120543669	AGCCAAGAATGGTGT[A/G]TATGCCTGGAGTCCC	9921
rs550815682	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120543023	AGAATGACATCTCAT[C/T]TATACAGTGAGGTTG	9921
rs550819494	snp	C/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120574312	GGGTTTGTCTCTTGA[C/T]ATTTTTCCAGGAATA	9921
rs550901785	in-del	-/ACTT	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120564748	TTCTGCCAACAAATA[-/ACTT]TATCTTCTCTGTTCG	9921
rs550982149	snp	A/G	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120545015	AACAATATATCTTCT[A/G]TGCTTGTCATTTTAT	9921
rs551011560	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120556134	TTTCTACTGAAGTTA[C/T]AAACTCTAGGTATCC	9921
rs551031413	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120571454	CTGCCTGTCGGAGCT[C/T]TATGCAGCATGGAGT	9921
rs551157897	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120565727	CCTAGCACATAGTAA[A/G]GATTAAGAGGAAATT	9921
rs551198468	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	RNF10	GRCh38.p7	12:120577998	TCTTCAGGGCGCCTT[A/G]TATTCAGGCGCAATA	9921
rs551343392	snp	A/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120558455	AAATGTGTATTAATT[A/T]AAAAAAAATCCTCAG	9921
rs551493864	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120545754	ATGTTGGCCAGGCTG[A/G]TCTCAAACTCCTGAC	9921
rs551504818	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120552193	TGAGGTCAAGAGTTG[A/G]AGACCAGCATGGTCA	9921
rs551733999	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120552811	AAGCAGAAAGGGAAT[G/T]GGTCTCGTTCTTTTT	9921
rs551792192	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120545719	ATTTTTTGTATTTTT[A/G]ATAGACATGGGGTTT	9921
rs551962000	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120540919	GAGTGTAGTGGTGCA[G/T]TCTCGGCCTTGCCGC	9921
rs552026387	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120573566	GGTATAAAAGATTAC[C/G]CGACGCCGAGTCATT	9921
rs552043605	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120536655	TCCCTCAAAAGATAG[A/C]AGGTAACCAGTCCTT	9921
rs552074205	in-del	-/GACTA	0.00557542	0.0525036	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120576287	TTGCACTCTGTTCAT[-/GACTA]GACAAGAATCACATA	9921
rs552108428	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120535747	TTTTATTTCTGTAAT[C/G]AAGTCTGTCAATATT	9921
rs552148097	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534309	ATTTCCCAGAATACC[G/T]CACCCCCTCTCCACT	9921
rs552169596	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120535408	CTTTCAAACTCAGAT[A/C]TCTTATTTAATAACC	9921
rs552171486	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120542207	ACTCTGTAGCCCAGG[A/G]TGGAGAGCAGTGGTG	9921
rs552197194	snp	C/T	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120559905	TATCTCTATGTTGGC[C/T]AGGCTGGTTTCGAAC	9921
rs552232744	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120548299	AGTTGGTGCTTAAAG[C/T]TGTGGAACTAAGTGA	9921
rs552233989	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120567250	GACCCACCTATTTTT[A/G]TTTCTAGTTTTTGTT	9921
rs552359270	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120575410	ATTTCCTAAGGAACA[A/G]ACAGCTTATGGTTTA	9921
rs552370828	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120554052	TGGGACTACAGGCGC[A/G]TGTCACCATGCCCGG	9921
rs552390558	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120561120	GGGCTTTTAAAGCTC[C/T]TTCTAGAGCTGAAAG	9921
rs552402281	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120567633	TTGAACCTGGGAGGC[A/G]GAGGTCTCAGTGAGA	9921
rs552414738	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120555490	TCTGGCCCAGTTGTA[C/G]TTTTTTTTTTTTTTG	9921
rs552533661	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120569132	ATGCCACCATGCCTG[A/G]CTAATTTTGTATTTT	9921
rs552539307	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577352	TGCTACCCCTAAGAT[C/T]GAGCTTGTTTTCAGT	9921
rs552553063	in-del	-/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120538070	AAAAGATTTCTGCAG[-/T]TATCTCATAAGCTGA	9921
rs552573659	snp	A/C			upstream-variant-2KB	RNF10	GRCh38.p7	12:120532416	GCCACCGTGCCCGGC[A/C]CCATATGCATGATTT	9921
rs552576895	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120544520	AAATCAGCTGGACAT[C/G]GTGGTGAGTGCCTGT	9921
rs552613982	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120568696	GGCCAGGCTGGTCTC[A/G]AACTCCTGGCCTCAA	9921
rs552778190	snp	A/G			upstream-variant-2KB	RNF10	GRCh38.p7	12:120533318	CCTCAGACTCCCAAA[A/G]GGCTGGAATTACAGG	9921
rs552993625	snp	C/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120536039	GGAAGGTGTTTTCAG[C/T]GACAGTGGGGATGTT	9921
rs552997931	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120568901	TGCTGGGATTCCAGG[C/T]GTGAGCCACTGTACC	9921
rs553007638	snp	C/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120542456	ACCAAGTCCAGCGCT[C/G]AAACTTTGCTTTCTA	9921
rs553036797	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120575177	GGAGGCACAGGTCAC[A/C]GTGAGCCAATATTGT	9921
rs553091042	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120550266	GTGGTTGGCTGAGAT[G/T]GGAGGGGCAAGCTAA	9921
rs553134212	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120536635	ATGCGTAGCTTTGCC[A/G]TAGATCCCTCAAAAG	9921
rs553141948	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120542300	CTAGGACTGCAGGTG[C/T]GTGCCACCACATTGG	9921
rs553151775	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120537515	CACCTGTAATCCCAG[C/T]TACTCGGGGGGCTGA	9921
rs553156250	snp	A/G	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120544156	TGCTGGAACCCGGGA[A/G]GTAGAGGTTGCAGTG	9921
rs553275731	snp	C/T	1.65685e-05	0.00287819	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563384	CCTTCGATGAAGAAA[C/T]CACGGAAGTTTGTTC	9921
rs553322474	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120545606	GCTGTGGCACGATCT[C/G]GGCTCACTGCAACCT	9921
rs553355220	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120570967	TAGAGTTACTGTAAC[A/G]ATGAAGCTCTTCCCT	9921
rs553484651	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120550746	GGACTATAGGTGCCC[A/G]CCACCATGCCCAGCT	9921
rs553564496	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120551454	CACCTGCCACTGCAC[C/T]CGGCTAGTTTTTTTT	9921
rs553574346	snp	C/G/T	6.59211e-05	0.0057408	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576683	ACTACTGGCCCAGGC[C/G/T]ACCTTCTCCATCTGG	9921
rs553707274	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577397	ATAGGAGGAGGAGTC[C/T]GGTACAGCTGCAGGA	9921
rs553718877	snp	A/G	1.65326e-05	0.00287507	intron-variant	RNF10	GRCh38.p7	12:120565221	TCTGCTTCTCTTTAT[A/G]GTAGGGTTCAGGGAT	9921
rs553818088	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120539332	TACTGGCATGTGCAT[C/T]ATTCCTGATACCACC	9921
rs554137645	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120539831	TGTGCATCAGAATCT[C/T]CTCAGGAACTTTTTT	9921
rs554304682	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120535443	CCCAGATCCATTCCT[C/T]TGTCGAAGAGGAAGT	9921
rs554370538	snp	A/G	0.000115326	0.00759274	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120566876	AGTTTCCTGCCTTCA[A/G]TTCTTATACCTGCTC	9921
rs554395452	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120559595	TCACCATGTTGGCCA[A/G]CATGGTCTCAATCTC	9921
rs554458953	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120553115	TTGAGATGTAGTCTC[A/G]CTCTGCCACCCAGGC	9921
rs554525938	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120547125	AGTAAATTACGTTTC[A/G]TACCATGCAATTATG	9921
rs554618329	snp	C/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120553529	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	9921
rs554685442	snp	C/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120541146	ATAGGCATGAGCCAC[C/T]GTGTCTGGCCATTTT	9921
rs554691852	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120568814	CTTGCTCAGTGCTGT[C/G]ATGCATTCATTAGCT	9921
rs554758174	snp	A/G	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120548598	TGGCTTTGCTCTAAA[A/G]GGGAGCAGAGATGTG	9921
rs554816365	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120568213	TTGGGCCACTGCACT[C/G]TAGCCTGGGCAACAC	9921
rs554865702	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120537380	GCCTGTAATCCCAGC[A/C]CTTTGGGAGGCCGAG	9921
rs554978507	snp	A/G	0.00438332	0.0466095	intron-variant	RNF10	GRCh38.p7	12:120560670	AATTCCTATTTAGCT[A/G]CACCATCGTGAGCTT	9921
rs555046606	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120576517	CCCACTCTGTGACTC[C/T]CAGTAATGAAAACTG	9921
rs555055497	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120562028	AACTTTTAAGTTCAG[A/G]GGTACAAATGCAGGT	9921
rs555090646	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120536676	ACCAGTCCTTTTGGT[C/G]AGTGTTGGAACTGGT	9921
rs555098334	snp	G/T	0.00279162	0.0372561	intron-variant	RNF10	GRCh38.p7	12:120559363	ATTTTTGTTTTTTTT[G/T]TGTGTGTGTGTTGTG	9921
rs555304549	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120563691	ACCCGGTGCTCTAAG[A/C]AGAGGAGCGCCACTA	9921
rs555406095	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120562874	GAGAGGCCATTCTAA[A/G]CCCTTGCCCTTCAAG	9921
rs555521202	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120567425	TCACACCAGAAGGCC[A/G]GGCGTGGTGGCTTAT	9921
rs555613339	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120538033	TAACAAAAGGGTACA[C/T]TCAAGCTCCGCATAA	9921
rs555655164	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120550350	GGAAGTATGAGTGGC[A/G]TCAGAGAAAGTGACA	9921
rs555795513	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120544737	TAGAAAGCAACCTAG[C/G]GATGTGTAAATGGCT	9921
rs555849220	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120536203	GAGGTGGGAGGATAG[A/C]TTGAGCCCAGGAGTT	9921
rs555883420	snp	A/C	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577521	ATTCTTTTGCTGCTT[A/C]ATAAAGTGACCTCTA	9921
rs555916791	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120557747	GGTGATTGAATATAT[C/T]TAAGCATCAGAAAGT	9921
rs555948416	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120545827	TACAGGCGTGAGCCA[C/T]TGCGCCCAGCCCCCA	9921
rs556080555	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120539898	TGGAGTTCAGTGGCG[C/T]GATCTCAGCTCACTT	9921
rs556152868	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120565876	TCTTTATTAAAGGGA[A/C]CAGCTATACACAGCA	9921
rs556211452	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120567482	CCAAGGCGGGTGGAT[C/T]ACGAGGTCAGGAATT	9921
rs556215427	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF10	GRCh38.p7	12:120532806	GAGTTACTCAAGGTG[A/G]ATTTCTACCCAACCA	9921
rs556361409	snp	G/T	0.00874735	0.0655527	intron-variant	RNF10	GRCh38.p7	12:120553475	TGGCACGATCTCAGC[G/T]CGCTGCAAGCTCCAC	9921
rs556454042	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120540509	CCTGGCAAGTTGTCC[A/G]CAAAACATTTCAAAA	9921
rs556550791	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120563078	CCAGGAAGGTTAGTG[C/T]GTTCCTGTTACTAAG	9921
rs556750137	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120559983	CGTGAGCCACCACAC[A/C]CAGCTGGCTTGGTCT	9921
rs556852798	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120547290	GCAAGGGAGCACACT[A/G]TATGGTTGTTTTAAG	9921
rs556896463	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120535950	GAGGCTAGAGTCCCG[A/G]TGTTCTTCATTTTAT	9921
rs556925002	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120542829	AAGTGCTGGGATTAC[A/G]GGGAGCCACCATGCC	9921
rs556931725	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120548742	TCGGCTCACTGCAAC[A/C]TCCGCTCTTGGGTTC	9921
rs556980136	snp	A/C	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120541594	CGCCCGCCACCAAGC[A/C]TGGCTAATTTTTTGT	9921
rs556989616	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120541795	TGCAGTGGTGCAAAC[A/G]TAACTGACTGAAACC	9921
rs557050408	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120574904	TGCACTCCAGCCTGG[A/G]CAACAAGAGCGAAAC	9921
rs557050468	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120548784	CTGCCTCAGTCTCCC[A/G]AGTAGCTGGGACTAC	9921
rs557051336	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120535494	TTGTGGGGTTAAGAG[C/T]GCAGACTATGAATTC	9921
rs557071865	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120555592	TGCCAGGTTCAAGCG[A/G]TTCTCCTGCCTCAGC	9921
rs557084986	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120572656	GCTGGAGTGCAATGG[C/T]GTGATCTCGGCTCAC	9921
rs557124568	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120542387	GCAAACTCGTGGACT[C/T]AAGTGATCCTCTTGC	9921
rs557125971	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120544049	CCTGGCCAATGTGGC[A/G]AAACTCCATCTCTAC	9921
rs557241098	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120575056	CCAGCCTGGCCAACA[C/T]GGTGAAACCCCGTCT	9921
rs557300202	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120568870	CAAGTGATCCTCCTG[C/T]CTGAGCCTCCCAGAG	9921
rs557358257	snp	A/G	0.000399281	0.0141238	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120576608	AGAAAGGAGGAAAGA[A/G]AAGAAAAAAACAGAA	9921
rs557375282	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120569959	GTGCAGTGGTGCGAT[C/T]TTGGCTCACTGCAAC	9921
rs557438979	snp	A/G/T	0.000116144	0.00761969	intron-variant	RNF10	GRCh38.p7	12:120563767	TGGGGAGCCTCCTGG[A/G/T]GACTGGCCAAGACTG	9921
rs557713229	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120562719	ACTAATTTACACTCC[C/G]CAGTGTCAGATTCTA	9921
rs557911235	in-del	-/A			intron-variant	RNF10	GRCh38.p7	12:120546225	CTTCATTATTGCAAG[-/A]AAAAAAACACTCTAC	9921
rs557930333	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120539268	TATGAAGTCCTAGGC[A/G]GTATTTTTCAATAAG	9921
rs557937223	snp	A/G			missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557641	TGGTGGCTTTGCCCA[A/G]ATCCAAATGGATGAA	9921
rs558050003	snp	A/G	0	0	intron-variant	RNF10	GRCh38.p7	12:120544793	TTCCACTTTTTGAGA[A/G]TTTGACATAATCACC	9921
rs558089921	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120548431	AGGAAAATTGCTGAA[A/T]GGTGTTGCAGAAGGT	9921
rs558188596	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120545302	TTCTCCTGCCTCAGC[C/T]TCCCGAGTAGCTGGG	9921
rs558211608	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120560071	AGGTGTGAGCCACTG[C/T]GCTGGTCCACCATTT	9921
rs558322305	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120541116	CCCGCCTCGGCCTCC[C/T]AAAGCATTGGGATTA	9921
rs558346394	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF10	GRCh38.p7	12:120532523	ATAATAGGCAAATTA[C/T]CTGGACTTTTGGAGT	9921
rs558374721	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120572267	GAGACAGGGTTTCAC[C/T]GTATTAGCCAGTAGG	9921
rs558453334	snp	A/G	0.00119737	0.0244387	utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534706	GTCGCCATGAAGGCC[A/G]AGAACCGCTGCCGCC	9921
rs558463759	snp	C/G	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120566716	GCAGTGAACAGAGAT[C/G]GTACCACTACACTCC	9921
rs558493372	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120547060	ACTGCTTTGTTTGTA[A/G]TTGCGAAATTGGGAA	9921
rs558520837	snp	G/T	0.0341408	0.126114	intron-variant	RNF10	GRCh38.p7	12:120553053	GTTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT	9921
rs558581290	snp	A/G	1.6477e-05	0.00287024	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546495	ACAACCAGTCCCGTC[A/G]CTCCAGTTCACAGAA	9921
rs558618178	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120559495	GTTCAAGAGATTCTC[C/T]TGCCTCAGCGTCCTG	9921
rs558636759	snp	A/G	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120560072	GGTGTGAGCCACTGC[A/G]CTGGTCCACCATTTC	9921
rs558637123	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120568149	ACTTGGGAGGCTGAG[A/G]TGGGGAGATGGCTTG	9921
rs558690124	in-del	-/AA			intron-variant	RNF10	GRCh38.p7	12:120566778	AAAAAAAAAAAAAAA[-/AA]TTGAATTCTGTAAAT	9921
rs558720085	in-del	-/C	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120570233	GCTCTATCACCCAGG[-/C]TGGAGCACAATGGCA	9921
rs558727240	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120574524	AAGGAGCTATTGGAA[A/G]AGCAGACTAAAAGGT	9921
rs558756988	in-del	-/TTGTT	0.00915404	0.0670315	intron-variant	RNF10	GRCh38.p7	12:120572586	AGTTATGCCAAATAC[-/TTGTT]TTGTTTTGTTTTGTT	9921
rs558798087	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120573903	CAGGGTTGTCAAACA[C/G]ACATGTACTGCCATT	9921
rs558882743	snp	A/G	1.64982e-05	0.00287208	intron-variant	RNF10	GRCh38.p7	12:120554701	GTCTAGCTTTTTCCT[A/G]TCTTTCCTATTTCTA	9921
rs558973733	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120550999	ATTTTTAATTTATTA[C/T]TTTTGAGACAGGGTC	9921
rs559104678	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120548015	TTTGTTAGATGTGGG[A/G]TCTGAGCAGAGAAAA	9921
rs559154863	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120553114	TTTGAGATGTAGTCT[C/T]GCTCTGCCACCCAGG	9921
rs559297815	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120536471	AAAACAAACAAAAAA[A/G]ACAGAAAATTGTAAG	9921
rs559321472	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120567151	ATCTTTCCCACTTGC[C/T]ATACTGACTGCTTTA	9921
rs559337839	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120556098	CAGCTTCAGTTGCAC[-/T]TTTCAAAGCCACTGA	9921
rs559393242	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120535575	ACTTACTTGTAAAGG[G/T]AGGTGGAGGTAATAT	9921
rs559456466	snp	C/T	1.70246e-05	0.00291754	intron-variant	RNF10	GRCh38.p7	12:120560928	ACCTTTTCACTTTCT[C/T]GGCGTTCTGTGGTGA	9921
rs559500809	snp	G/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120542796	GGCCTCATGTGATCT[G/T]CCTGCCTTGGCCTCC	9921
rs559573698	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120576177	AATTCTGAGGAACTC[G/T]TCCAAGATACAGTGG	9921
rs559575328	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120555227	CACTCTGTTGCCCAG[A/G]CTGGAGTACAGTGGT	9921
rs559584191	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120556008	TGTCCAGGCTTGTCT[C/T]AAACTCCCAGCTTCA	9921
rs559613963	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120561639	GTGTGGTAGATAGAA[C/G]TATCCCCTTTCATGG	9921
rs559615122	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120535557	AGTGAGTGCCCCGAG[A/T]TTACTTACTTGTAAA	9921
rs559619595	snp	A/G/T	1.6473e-05	0.00286988	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563029	GAACAACTGGTGCTG[A/G/T]TGGCTCCCTTGGCGA	9921
rs559815852	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120575567	AGTTAGTCAAGGTAG[C/G]TCTGAAAAAGAAGTT	9921
rs559882734	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120550527	AAAATAAGGGATGAC[C/T]TGGAAGTCTTGGGCT	9921
rs560028048	snp	A/G	0.000798403	0.0199641	downstream-variant-500B	RNF10	GRCh38.p7	12:120577848	GTGTTTCTGTTAAAT[A/G]TGTATGGTACTTTCA	9921
rs560144503	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120550891	ATGAGCCACCACACC[C/T]GGCCCAGAATGCGGC	9921
rs560169183	snp	G/T	0.000693619	0.0186099	intron-variant	RNF10	GRCh38.p7	12:120571320	TTGTGAAGCAGCCCA[G/T]GGGTATTTAACATGA	9921
rs560302439	snp	C/G			intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120576233	TCTTGAGTTGGTACA[C/G]GGTGGCTAATTAGAT	9921
rs560306498	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120544853	GTATTATATTAAACT[A/G]ACAAAAAATTAGAAG	9921
rs560400913	snp	A/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120537730	TTGACCATGTTTGCC[A/T]CCGCCAGTGTCTGCT	9921
rs560504748	snp	A/T	0.00318978	0.0398085	intron-variant	RNF10	GRCh38.p7	12:120545550	ATTTATTTAATTAAA[A/T]TTTTTTTTGAGATAA	9921
rs560520350	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120559504	ATTCTCCTGCCTCAG[C/T]GTCCTGAGTAGCTGA	9921
rs560534880	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120558122	TTAAAATAGCATTTC[A/G]GTCTCTGGGGAAAAG	9921
rs560549810	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB	RNF10	GRCh38.p7	12:120532981	CTGTTTCTACTTTTT[A/T]AAAAAAAGTTTAGAC	9921
rs560641005	snp	A/G	3.86384e-05	0.00439519	intron-variant	RNF10	GRCh38.p7	12:120565561	TCATCTTTGACTAGC[A/G]CTGCTGTACGTCGTT	9921
rs560659785	snp	C/G	1.64738e-05	0.00286995	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120552558	TGGTCCTAAGAAGAT[C/G]AACCTGAACCACTTG	9921
rs560683610	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RNF10	GRCh38.p7	12:120533977	GCGCCACTGCACTCT[A/C]GCCTGGGCGACAGAG	9921
rs560694811	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120551873	ACTGGGTAATTTATG[A/G]AAAAGAGTGGCTTAA	9921
rs560812100	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120546015	TATAGTAATTTAAAA[A/G]GGAATCTCTTCTGTC	9921
rs560833897	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120572696	CGCCTCCCGGGTTCA[A/G]GCAATTCTCCTGCCT	9921
rs560937650	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120547666	ACGGGAGGTGGTAGT[A/G]CGTTTATTGGTTTGA	9921
rs560949011	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120540170	GTCTCACCATGTTGC[C/T]CAGGCTGGTCTCAAA	9921
rs560976270	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120553848	CTAGACTGAAGTAAC[C/T]GTTTTGTACTTTATA	9921
rs560992688	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120560129	GTTGGTTTGAGCTTT[G/T]CTTTTTCTGTGTGTG	9921
rs561001183	snp	A/C	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120548153	TGAGATAAAGAACTT[A/C]AGTTTGGAAATGTTA	9921
rs561180434	snp	A/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120567043	CAAAGCTTTGGTGTC[A/T]GAGTTTACAACCCCG	9921
rs561223738	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120575282	TTCCTCCGACAGCTC[A/G]ATGTTTTTAGGGGTC	9921
rs561262253	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120574884	TAAGCCAAGATTTGC[A/G]CCATTGCACTCCAGC	9921
rs561333834	snp	A/G	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120542113	CCTCGTGATCCACCC[A/G]CCTCAGCATCCCAAA	9921
rs561339956	in-del	-/TT			intron-variant	RNF10	GRCh38.p7	12:120540870	TTTTTTTTTTTTTTT[-/TT]GAGACAGAGTTTTGC	9921
rs561405895	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120541473	GGAGTCTCACTCTGT[C/T]GCCCAGACTGGAATG	9921
rs561437589	snp	C/T	0.00358779	0.0422022	intron-variant	RNF10	GRCh38.p7	12:120556455	AGAATGGCGTGAACC[C/T]GGGAGATGGAGCTTG	9921
rs561500717	snp	A/T	0.0023933	0.0345097	upstream-variant-2KB	RNF10	GRCh38.p7	12:120534092	ACATTATTATCAGTG[A/T]ATATTATTATTGTTA	9921
rs561570637	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120568946	ACTTTTTGATGCTTA[C/T]GTCTGATTTCTCAGG	9921
rs561629649	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120556329	CACGGGGTCAGGAGA[G/T]CGAGACCATCCTGGC	9921
rs561735554	snp	C/T	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120555289	AGGGTTCAAGCAATT[C/T]TCATGCCTCAGCCTC	9921
rs561765258	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120560993	GGGTGAGATGATGGA[C/T]GCTGGGGATTAAGTT	9921
rs561805500	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120543630	AACATGGCAAAACCC[C/T]GTCTATATCAAAAAT	9921
rs561848317	in-del	-/GTG	8.23974e-05	0.00641809	cds-indel, nc-transcript-variant	RNF10	GRCh38.p7	12:120552653	GGGAAAGAGGAACAA[-/GTG]GTGGGGACATAAGCC	9921
rs561903360	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120543015	GTTTGGAGAGAATGA[C/T]ATCTCATTTATACAG	9921
rs561993089	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120545236	CCCAGGCTGGAGTGC[A/C]GTGGCACGATCTCAG	9921
rs562109260	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120537523	ATCCCAGCTACTCGG[C/G]GGGCTGAGGCAGGAG	9921
rs562142512	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120538327	ATGGCCATTTGCTTC[C/G]TAGCTACATGATTAA	9921
rs562176362	snp	A/G	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120550940	TGTTAATATAAAAAA[A/G]GAAGTTATCTGACTG	9921
rs562183459	snp	C/T	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120569726	TATTTTTAGTAGAGA[C/T]GGGGTTTCGCCATGT	9921
rs562243613	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RNF10	GRCh38.p7	12:120577951	AAGTCTCCCGCCATT[C/T]CTACTTCCTGTGAGT	9921
rs562314162	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120556117	CAAAGCCACTGATGT[A/G]TTTTCTACTGAAGTT	9921
rs562346441	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120550679	TCGGCTCACTGCCAG[C/T]TCTGCCTCCTGGATT	9921
rs562427700	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120572468	GGTAAGGAGGGTTCC[C/G]AAGTCAAGGAACATG	9921
rs562462308	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120571998	ATGGACAGCTTGACA[C/T]GTGCCCTTGTAAGAA	9921
rs562510494	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120548852	TTTTTTTGTATTTTT[A/C]GTAGAGACGGGGTTT	9921
rs562588972	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120566364	AACTATATTAAAGAC[A/G]TTATAGAAGGACAGT	9921
rs562692977	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120538117	ATTCTGCTGGGAATC[A/G]TTGAAAGGACCTCTT	9921
rs562710402	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120539457	GTGCTTGTCAACTAC[C/T]CTGGATGATGGGTAA	9921
rs562712821	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120553668	TCGGCCTCCCAAAGT[G/T]CTGGGATTACAGGCG	9921
rs562787942	snp	A/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120558428	TAAATGTTTAGCAAC[A/T]TAAAACATTAAAAAT	9921
rs562906899	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120565687	GCTTGCTTGCAAATA[C/T]AATGAGTTAATATGG	9921
rs562921637	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120540311	TGGGTCCTGGGCATT[A/C]ATAATTTAAAAAGTC	9921
rs562942343	snp	G/T			utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534548	GCCTCCCCTTCCCCC[G/T]CAGCCTCCGCCCCGC	9921
rs562970971	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120552776	CTGTGAGAGGCTTTT[C/T]TTAAGCTATTGTGGG	9921
rs562972801	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120553175	TGCAACCTCTGCCTC[A/C]CGGGTTTAAGTGATT	9921
rs563009357	snp	G/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120559141	TTTAGCAGAGATGAG[G/T]TCTTGCTATGTTGAT	9921
rs563097281	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120572073	ACAGTTTTTTTTTTT[G/T]TTTCCTCTTCTCCAA	9921
rs563231763	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120573534	CTATTTGGATACTGT[C/G]TCAGTCCATTTGTGT	9921
rs563354054	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120567782	GGGAAGATAAAAGTA[A/G]TTTGTAGAACAAGAA	9921
rs563407703	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120554459	GGTTAATTTTAGTTC[A/G]AGGGATGCCTTTGGG	9921
rs563410057	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120542698	GCTGGGATTACAGGC[A/G]TGTGGCACCACACCT	9921
rs563493059	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120546708	CAAGAGGTAGAGGAA[-/T]TAGATAATCAAAGCA	9921
rs563578827	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120571107	TGTAATTTTCCAGAC[A/C]TGACTCAGGGCTCAC	9921
rs563626394	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120569636	CTCTGCGTCCCAGGT[G/T]GAAGCAATTCTTGTG	9921
rs563626429	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120561960	TCTTAGATTTCTGTT[C/T]TGGAAGTTTTTTGTA	9921
rs563662565	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120569062	TGCAACCTCTGCCTC[A/C]TGGGTTCAAGCGATT	9921
rs563764429	in-del	-/A	0.3746	0.216737	intron-variant	RNF10	GRCh38.p7	12:120552083	GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	9921
rs563769184	snp	A/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120535697	ATGTCTATTGTTGTG[A/T]GTTGGACTATAGGAT	9921
rs563786892	snp	A/G	0.000559929	0.0167228	intron-variant	RNF10	GRCh38.p7	12:120562940	GTTCTCTCTGGCCAC[A/G]TTAGACTCGGGAAGA	9921
rs563897287	in-del	-/T	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120553188	CCCGGGTTTAAGTGA[-/T]TTTTTTTGCCTCAGC	9921
rs563897339	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120542592	GAGTCTCACTCTGCT[G/T]CCCAGGCTGGAGTGC	9921
rs564044933	in-del	-/T			upstream-variant-2KB	RNF10	GRCh38.p7	12:120532429	GCCCCATATGCATGA[-/T]TTTCTAAATCTCAGT	9921
rs564156510	snp	A/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120555409	CTGTTTTTGAACTCC[A/T]GACTGCAAGTGATCC	9921
rs564178717	snp	A/G	0.00438332	0.0466095	intron-variant	RNF10	GRCh38.p7	12:120556371	AACCCCGTCTCTACT[A/G]AAAAAAAAAATTAGC	9921
rs564249972	snp	A/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120537153	TGTCCTACAAAAAAA[A/T]AAATGAGCCGGGCGT	9921
rs564251949	snp	C/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120544244	AAAAAAAAGATAAAC[C/G]AGGCATGGTGGTTCA	9921
rs564313220	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120543698	CCAGCTACTTGGGGG[G/T]CTGAGGCAGGAGGAT	9921
rs564339766	snp	A/C	0.00636936	0.0560724	intron-variant	RNF10	GRCh38.p7	12:120537608	ACTCCAGCCCGTCTA[A/C]AAAAACAAAAACTCA	9921
rs564432848	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120570416	GTCTTGAACTCCTGA[C/G]CTCAGGTGATCCACC	9921
rs564496675	in-del	-/A	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120541205	AATCTGGCTTTACCT[-/A]AATCTATGCAAACCG	9921
rs564594622	snp	A/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120571121	CCTGACTCAGGGCTC[A/T]CTCATCTCTCTTGTT	9921
rs564604046	in-del	-/T	0.0023933	0.0345097	intron-variant	RNF10	GRCh38.p7	12:120545493	CACCGCGCCTGGCCA[-/T]TTTTAAAAAGGATAT	9921
rs564635792	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120550988	TGTATTTAATTATTT[C/T]TAATTTATTATTTTT	9921
rs564739193	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RNF10	GRCh38.p7	12:120532833	ACCACGCCTAAACGA[A/C]ATTGTTTATCTGACC	9921
rs564775362	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120551730	CCTTGAATTCCTGGG[C/G]TCAAGTGCCCCTCTT	9921
rs564802488	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120559241	GGCTGGAGTGCAATG[A/G]TGTGATCTCGGCTCA	9921
rs564838100	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120566409	GTTTTAGCTTTTGTC[G/T]GCATCCTCTAGACCT	9921
rs564870572	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120549535	CACAGCTGTAATCCC[A/G]GCACTTTGGGAGGCC	9921
rs564969959	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120571865	GCCAAAGCAGCTTCC[G/T]TGGAGCTGGGTGGGG	9921
rs564986875	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120559758	TGGAGTGCAATGGTG[C/T]GATCTTGGCTCACTG	9921
rs565208905	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120553801	TTTCCTTTTGTGTGG[C/T]CCTAGTCATAATTGA	9921
rs565345848	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120542191	TTTGAGACAGAGGCT[C/T]ACTCTGTAGCCCAGG	9921
rs565354526	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120546752	GAGAGGGTTAACCAG[A/G]TTTGAAACCTTGCCT	9921
rs565435912	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120548438	TTGCTGAAAGGTGTT[G/T]CAGAAGGTGATCAGT	9921
rs565455489	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120541330	TTTCTTTATATACCT[A/G]TCCTCGTAGAATCTC	9921
rs565541805	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120535082	TTTCTTTTATAGCTC[C/T]TACCTGCCCTTTTCC	9921
rs565553217	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120574290	GCATCCCTGCTTGAA[A/C]CCCATGGGGTTTGTC	9921
rs565613223	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120535432	AATAACCTGGTCCCA[C/G]ATCCATTCCTCTGTC	9921
rs565716544	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120559917	GGCCAGGCTGGTTTC[A/G]AACTCCTAACTTCAG	9921
rs565733942	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120547065	TTTGTTTGTAGTTGC[A/G]AAATTGGGAAATAAC	9921
rs565747491	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120535825	CCAAGTACTAGGTGA[A/C]GTTTTTACCTCTGTT	9921
rs565783353	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120560227	CATGATCTTGGCTCA[C/T]TGCGACCTCTGCCTC	9921
rs565815526	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120561150	GGAGCAAGTCAAAAT[G/T]ATTTTATAACTAATT	9921
rs565953333	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120574559	AGGGGCTGTTGAAGC[A/G]GTGTCAGGAGAGAGT	9921
rs565971433	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120562105	CACCCAGGTATTAAG[C/T]TTAGTACCCATTGGT	9921
rs566035150	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120555509	TTTTTTTTTTTGAGA[C/T]GGAGTTTCGCTCTTG	9921
rs566059337	snp	C/G	0.0023933	0.0345097	intron-variant	RNF10	GRCh38.p7	12:120568745	CCTCCCAAAGTGCTG[C/G]GATTGCAGGTGGGAG	9921
rs566208714	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120549133	TAGATAGGAACTCTA[C/T]CAGTTCATCCCCAGT	9921
rs566544753	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120537176	CCGGGCGTGGTGGCA[C/T]GCACCTGTAGTCCCA	9921
rs566610168	in-del	-/A	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120565929	GATGGAAATTTTGAT[-/A]AGACTAGGAAATGCA	9921
rs566669417	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563413	TCTCTGGACACTCCT[C/T]CTAGACCTCTTGCTC	9921
rs566739866	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120564475	AAAATACAAAAAAAA[A/G]TTAGCTGGGTATGAT	9921
rs566810897	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120544698	TTATGTTGTTAGAGT[A/G]TAAATAAATCGGTGT	9921
rs566913888	snp	G/T	0.00318978	0.0398085	intron-variant	RNF10	GRCh38.p7	12:120556693	GGTAGATTACTTCTA[G/T]ACCCTTTTTAGGCCT	9921
rs566958359	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120538395	TGCCCTTCATTTGTA[C/T]ACAGGAAATATGTAA	9921
rs566975114	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120550666	CAGTGGCGTGATCTC[A/G]GCTCACTGCCAGCTC	9921
rs566992559	in-del	-/ATC			intron-variant	RNF10	GRCh38.p7	12:120552916	CTTAAATAACTTAGT[-/ATC]ATGATAAGGTAGAAA	9921
rs567026904	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120539621	GTGGCCCTTAATTTG[A/G]TAATGGGGGGAGGCT	9921
rs567078489	in-del	-/T			utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577184	CAGTTTGAATTGCAG[-/T]TTTTTTTTTTTCTGA	9921
rs567100494	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120545147	TTTTCAGAATTGAAC[A/G]CATATTATAATTGAA	9921
rs567167105	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120552325	GAGTCACTTGAACCT[A/G]GGAGGCAGAGGTTGC	9921
rs567206982	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120572168	GCCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC	9921
rs567208111	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120574928	GCGAAACTCCATCTC[A/G]AACAAAACAAAAAAA	9921
rs567229750	snp	G/T	0.00318978	0.0398085	intron-variant	RNF10	GRCh38.p7	12:120566435	GACCTTTGGGGGTAC[G/T]CATGTGTGATGTCCT	9921
rs567298193	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120567003	GGTGAAATTTAATGA[A/G]TTCACCCATCAGTTA	9921
rs567327056	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120552056	GCCACTGCACTCCAG[C/T]CTGGGTGACAGAGTG	9921
rs567371153	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120565821	AATGCTGGGGGCCAT[C/T]GTTCCCCATGCTCTC	9921
rs567419146	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120573573	AAGATTACCCGACGC[C/T]GAGTCATTTATCAAA	9921
rs567480015	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120574319	TCTCTTGATATTTTT[C/T]CAGGAATAAAATGTT	9921
rs567582134	snp	A/C	0.00318978	0.0398085	intron-variant	RNF10	GRCh38.p7	12:120546975	TATATCTATAGTCTC[A/C]AATTTTTTTTAGGAG	9921
rs567649720	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	RNF10	GRCh38.p7	12:120533681	TGAGATAGACTAAAG[A/G]CCATAAATCAATTGG	9921
rs567734248	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534437	CTGTGTCGGAGACAC[C/T]AGTCCCCGACACCGA	9921
rs567805743	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120567438	CCGGGCGTGGTGGCT[C/T]ATGCCTGTAATCCCA	9921
rs567885135	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120567878	GTGTGTGTGTGTGTG[C/T]GTGTATGTATATATA	9921
rs567970688	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120559971	CAAAGTGCTGAACGT[A/G]AGCCACCACACCCAG	9921
rs568001438	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120540352	ATTCTGGTGTGCAGC[A/C]AGGATTGAGAACCAC	9921
rs568077117	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120537295	TCTAGCCTGGGTGGC[A/G]GAGTGAGACCCCGTC	9921
rs568102875	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120541751	TTTTTTTTTAGAGAC[A/C]AGCTCTCGCTCTGTC	9921
rs568207597	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120542375	CCCAGGCTGGTCGCA[A/G]ACTCGTGGACTCAAG	9921
rs568321267	in-del	-/A	0.00597247	0.0543191	intron-variant	RNF10	GRCh38.p7	12:120547157	TAGAATAAGACAGAT[-/A]AAAAAAATATAGACT	9921
rs568400628	in-del	-/TTGTT	0.0019972	0.0315375	intron-variant	RNF10	GRCh38.p7	12:120572585	AGTTATGCCAAATAC[-/TTGTT]TTGTTTTGTTTTGTT	9921
rs568401107	snp	A/G	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120574978	GGCACAGTGGCTCAC[A/G]CCTATAATCCCAGCA	9921
rs568422021	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120549927	AATTGTTGGAGTCAG[A/G]ACTAAACCTGGGGAA	9921
rs568482359	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120576518	CCACTCTGTGACTCT[C/T]AGTAATGAAAACTGG	9921
rs568611506	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120570806	AAGCTGAGCTGATTA[A/C]ATTTTATCTTTTTCT	9921
rs568640360	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120535419	AGATCTCTTATTTAA[C/T]AACCTGGTCCCAGAT	9921
rs568642987	snp	C/T	0.000188058	0.00969504	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577208	TTTCTGACACATGGC[C/T]AGGCTGTGGTGCCAG	9921
rs568681656	snp	C/T	0.00636936	0.0560724	intron-variant	RNF10	GRCh38.p7	12:120556082	GCGTGAGCCACCACG[C/T]CCAGCTTCAGTTGCA	9921
rs568766573	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120556979	AACACAGTGAAACCC[C/T]GTCTCTACTAAAAAA	9921
rs568804021	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120537290	TGCACTCTAGCCTGG[A/G]TGGCAGAGTGAGACC	9921
rs568815986	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120537735	CATGTTTGCCACCGC[C/T]AGTGTCTGCTTTTCT	9921
rs568920230	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120564482	AAAAAAAAATTAGCT[A/G]GGTATGATGATGTGC	9921
rs569077331	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120556787	TAATGTAGAACCCCC[A/G]ACATACCTGTTGTGT	9921
rs569154073	snp	A/C	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120565116	TCACTTGCCACTCAC[A/C]TGTGAGTTCAGCATC	9921
rs569301678	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120559916	TGGCCAGGCTGGTTT[C/T]GAACTCCTAACTTCA	9921
rs569321207	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120551359	GAGTGCAATGGTGTG[A/C]TCTTGGCTCACTGCA	9921
rs569415612	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF10	GRCh38.p7	12:120533317	TCCTCAGACTCCCAA[A/G]GGGCTGGAATTACAG	9921
rs569437479	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120556918	AGGACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA	9921
rs569474160	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120555297	AGCAATTCTCATGCC[C/T]CAGCCTCCTGAGTAG	9921
rs569475848	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120539645	GGAGGCTGAGATATA[C/G]CTACTGCTACTTGGT	9921
rs569567950	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120541108	GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGCAT	9921
rs569589319	in-del	-/AGATCT	0.00478085	0.0486577	intron-variant	RNF10	GRCh38.p7	12:120549089	GTCCTTGAGTCCTTG[-/AGATCT]AGTGAGAAGTGGAGC	9921
rs569636363	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120559867	CGCCCAGCTAATTTT[G/T]TGTATTTTTAATAGA	9921
rs569687216	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120573664	AGTGCCTCAGGCTGC[C/T]TCCACTCATGGTACA	9921
rs569718543	snp	A/G	0.00279162	0.0372561	intron-variant	RNF10	GRCh38.p7	12:120553032	CCTTTATAAGGAAGA[A/G]GAAAGGTTTTTTTTT	9921
rs569756570	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120541528	CTAGCCCCGCCTCCC[A/G]GGTTCACGCCATTCT	9921
rs569813786	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120568032	GGAGGCCAAGGTGGG[C/T]AGATTCCCTTGAGCT	9921
rs569929179	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120535341	ACCCTTTAATGTTGA[A/G]TTAACATTGGATAGT	9921
rs569990317	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120541620	TTTGTATTTTTAGTA[C/G]AGATGGGGTTTCACC	9921
rs570085274	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120574371	TTTGCAGTTGGGGCT[C/T]ATAGTGGCCTTCAGC	9921
rs570191310	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120560493	TACAATGCTGTAACA[A/G]TAAACGCGTGACTAA	9921
rs570480825	snp	A/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120535966	TGTTCTTCATTTTAT[A/T]TCGAAGTTTGTACTA	9921
rs570506510	snp	A/G	1.64738e-05	0.00286995	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575706	GAGGATGGTCCACTG[A/G]TGAAGGGGGAGTTTG	9921
rs570515932	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120543051	TTGACAGACTATGGG[C/T]GTGAAGTGGTTGCTT	9921
rs570575633	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120542452	AGCCACCAAGTCCAG[C/T]GCTGAAACTTTGCTT	9921
rs570698777	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120536587	CCGTGTCAGGAAATG[A/G]CATGTATGCAGACTG	9921
rs570736393	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120544056	AATGTGGCGAAACTC[C/T]ATCTCTACTAAAAAT	9921
rs570757175	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120569790	TGATCCGCCTGCCTC[A/G]GCCTCCCAGTGTGCT	9921
rs570760896	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120537909	GGATATTGGCTGATT[G/T]TTAAAGTTGAAACTA	9921
rs570773925	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120569315	CATTCTTAACAAAGT[A/G]TCCATCATTGGAATA	9921
rs570880433	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120556158	GGTATCCCCTTGTTG[A/G]TCCTAGTAGGGTATC	9921
rs570911445	snp	A/T	0.00279162	0.0372561	intron-variant	RNF10	GRCh38.p7	12:120556632	AACTTAAGTTTTATT[A/T]AAAAAAAATGAAGTC	9921
rs571036511	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120538506	ATTTATATAACATTC[C/T]TTTTCTTGATTATAT	9921
rs571056579	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120543772	GCCACTGCACTCCAG[C/T]CTGGGTGACAAAAGT	9921
rs571073756	snp	C/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120550635	GAAGTCTCGCTCTGT[C/T]GTCCAGGCTAGAGTG	9921
rs571133541	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577159	TGGGAATAAAATGGA[A/T]TTAGGACACCCAGTT	9921
rs571147877	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120565733	ACATAGTAAGGATTA[A/C]GAGGAAATTCAGCCT	9921
rs571177306	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RNF10	GRCh38.p7	12:120578007	CGCCTTGTATTCAGG[C/T]GCAATAAGAGCGGAA	9921
rs571208759	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120558480	CCTCAGATATGGGTG[A/G]ATTTTTGAACCAGGC	9921
rs571320243	in-del	-/TTTA			intron-variant	RNF10	GRCh38.p7	12:120542553	TTTTTAAGTTCTAAC[-/TTTA]TTTATTTGTTTTTTG	9921
rs571332935	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120571496	AGATTATGTCATGGA[C/T]GTCCGCTCTGTTGGA	9921
rs571356346	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120566535	GGGAGGCCAAGGTGG[A/G]CAGATCACTTGAGCT	9921
rs571374562	snp	A/G	0.0158469	0.0875917	intron-variant	RNF10	GRCh38.p7	12:120567883	TGTGTGTGTGTGTGT[A/G]TGTATATATATATAT	9921
rs571395311	snp	G/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120540463	TCATCTTATCACTCC[G/T]GTTCTACCCTCGAGT	9921
rs571396054	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120572475	AGGGTTCCGAAGTCA[A/C]GGAACATGAAATAAT	9921
rs571400626	snp	A/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120569151	ATTTTGTATTTTTAG[A/T]AGAGACAGGGTTTCT	9921
rs571452281	snp	C/G	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120551387	GCAACCTCTGCCTCT[C/G]GGGTTCAAGCGATTC	9921
rs571582181	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120550619	TTTTTTTTTTTTGGA[C/T]GAAGTCTCGCTCTGT	9921
rs571600752	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120552817	AAAGGGAATTGGTCT[C/T]GTTCTTTTTCTGTTC	9921
rs571664771	snp	C/G	0.00835141	0.0640778	intron-variant	RNF10	GRCh38.p7	12:120545753	CATGTTGGCCAGGCT[C/G]GTCTCAAACTCCTGA	9921
rs571719651	snp	C/T	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120540386	TCTGAGATTTAAAAC[C/T]TCACCCATAGTTCCT	9921
rs571768591	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120572968	TTTGAACTTTATTTT[C/G]AAATACAGAGTTGAA	9921
rs571802800	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120539606	AACTGTGAAAAACTT[A/G]TGGCCCTTAATTTGG	9921
rs571840784	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120537308	GCAGAGTGAGACCCC[A/G]TCTCAAAACAAGAAA	9921
rs571845293	snp	C/G/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	RNF10	GRCh38.p7	12:120534332	TCTCCACTATATATA[C/G/T]AGTCCATCCGGGTTC	9921
rs571894300	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534711	CATGAAGGCCGAGAA[C/T]CGCTGCCGCCGCCGA	9921
rs571908288	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RNF10	GRCh38.p7	12:120533417	TCTCGCTATATTCCC[C/G]AGGCTGGTCTGGAAC	9921
rs571937986	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120553683	GCTGGGATTACAGGC[A/G]TGAGCCACGGCACCC	9921
rs571946868	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120567256	CCTATTTTTGTTTCT[A/G]GTTTTTGTTTGAGAT	9921
rs572041894	snp	A/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120545936	ACAGTTTTGCTGTTA[A/T]TGCCTTTTGAATATA	9921
rs572048755	snp	C/T	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120546499	CCAGTCCCGTCGCTC[C/T]AGTTCACAGAAAAGC	9921
rs572109180	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120550631	GGACGAAGTCTCGCT[C/G]TGTCGTCCAGGCTAG	9921
rs572170365	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120573314	TTGTCAAGTCTCTTT[A/G]GTCTCCTTTGATCTA	9921
rs572185670	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120554232	TTTTAGTAGAGATGG[A/G]GTTTCACCCTGTTGG	9921
rs572209422	snp	G/T			missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557456	TCTGTGCATAAGAAG[G/T]ATCTCAAGAGGTGAG	9921
rs572224223	snp	C/T	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120553802	TTCCTTTTGTGTGGC[C/T]CTAGTCATAATTGAA	9921
rs572224644	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120560579	AGACCTTATTTTAAG[A/G]CCATTGTTAAATTAT	9921
rs572225376	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120559494	GGTTCAAGAGATTCT[A/C]CTGCCTCAGCGTCCT	9921
rs572277032	snp	C/T	0.0023933	0.0345097	intron-variant	RNF10	GRCh38.p7	12:120573915	ACACACATGTACTGC[C/T]ATTCCCACTGGGATC	9921
rs572334710	snp	C/T	1.6659e-05	0.00288604	intron-variant	RNF10	GRCh38.p7	12:120567022	ACCCATCAGTTAGAC[C/T]TTATGCAAAGCTTTG	9921
rs572482107	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120547573	TGCTGGGATTACAGG[C/T]ATGAGCCACCACACC	9921
rs572599540	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120544981	ATGCATAAAAATGCT[C/T]ACAGAGTAGTAAGCA	9921
rs572671984	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120542055	GTATTTTTAGTAGAG[A/G]CAGGGTTTCACCATG	9921
rs572684464	in-del	-/G	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120550216	ACTGGCTGCTGTGTT[-/G]GGACATTACAGCTGT	9921
rs572702575	snp	C/T	0.00358779	0.0422022	intron-variant	RNF10	GRCh38.p7	12:120548504	TGAAAGTTGACCATT[C/T]GATTTGAAAATGGCA	9921
rs572722659	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120575212	TTGCACGCCAGCCTG[A/G]GCAACAAGAGCTAAA	9921
rs572736357	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120535576	CTTACTTGTAAAGGT[A/G]GGTGGAGGTAATATA	9921
rs572961119	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120537518	CTGTAATCCCAGCTA[C/T]TCGGGGGGCTGAGGC	9921
rs573029182	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120562808	TTGAGATATTTAAGC[A/G]CCTAATTCCTTCCCA	9921
rs573155122	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120556261	GAACTCTCGCCGGGC[A/G]CGGTGGCTCACGCCT	9921
rs573193650	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120555707	CTCCATGTTGGTCAG[A/G]CTGGTCTTGAATTCC	9921
rs573210304	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120545696	GTGCCCGCCACCATG[C/T]GCGGCTAATTTTTTG	9921
rs573274340	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120541952	GCTCACTGCAAGCCC[C/T]GCCTCCCAGGTTCAC	9921
rs573307610	snp	A/G	0.00159617	0.0282053	intron-variant	RNF10	GRCh38.p7	12:120544169	GAGGTAGAGGTTGCA[A/G]TGAGCCGAGATTGCG	9921
rs573327218	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120570032	TGAGTAGCTGTGTAG[C/T]GTGCCACCATGCCTG	9921
rs573382345	snp	A/G	0.00119737	0.0244387	intron-variant	RNF10	GRCh38.p7	12:120551456	CCTGCCACTGCACCC[A/G]GCTAGTTTTTTTTTT	9921
rs573418646	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120575409	CATTTCCTAAGGAAC[A/C]AACAGCTTATGGTTT	9921
rs573448320	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577431	CAGGGCCATCTGAAG[C/T]GGTAGCATTGCCACC	9921
rs573477453	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120564765	TTTATCTTCTCTGTT[C/T]GTCCCCCTCAGCTGT	9921
rs573514251	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120570980	ACGATGAAGCTCTTC[C/T]CTCTTCCTGTACCGG	9921
rs573515852	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120565251	TTCTTGTGGCTAGAC[A/G]CCCAGTGGGGGAGGA	9921
rs573811063	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120545427	TCAATCTCCTGACCT[C/T]GTGATCCGCCCACCT	9921
rs573899368	snp	A/G	0.000929973	0.0215435	intron-variant, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120539375	TCATTCAGAATTACT[A/G]ATTTCAGCTGGATTC	9921
rs573930167	in-del	-/TTTC			intron-variant	RNF10	GRCh38.p7	12:120539137	GCATTTTACAGAAGT[-/TTTC]TTTCTTAATCCTCAT	9921
rs573973292	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120543077	TGCTTTCAAAATTTG[G/T]TCTCTGATTTATTAA	9921
rs574034637	snp	C/T			synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563878	CGGGAGTACGGCAGC[C/T]TGGAGAGGAGCCCCG	9921
rs574045769	snp	A/G	0.000148271	0.00860893	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120566884	GCCTTCAATTCTTAT[A/G]CCTGCTCCTCTGATT	9921
rs574398473	in-del	-/TTGTTTTGTT			intron-variant	RNF10	GRCh38.p7	12:120572586	AGTTATGCCAAATAC[-/TTGTTTTGTT]TTGTTTTGTTTTGTT	9921
rs574403517	snp	A/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120540846	CTTGCTGAGTGCCAG[A/T]TTACTTTCTTTTTTT	9921
rs574404871	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120534974	CCCAAGAGCGGTAAG[A/G]ACGGGCCTGCGGCAG	9921
rs574411010	snp	C/G			downstream-variant-500B	RNF10	GRCh38.p7	12:120577793	GGATGAGGGTGTTCT[C/G]GCCTCCAGATGAGGG	9921
rs574435683	in-del	-/AA	0.0387552	0.1337	intron-variant	RNF10	GRCh38.p7	12:120536263	CCTCGTCTCCATAAG[-/AA]AAAAAAAAAATTAGC	9921
rs574450010	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120554437	TGTTTGATGGAGTCA[C/T]GGTCTAGGTTAATTT	9921
rs574467524	snp	C/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120541181	TCTTAATAAGCCCTT[C/G]CCATGTAGAATCTGG	9921
rs574499882	in-del	-/C	0.00557542	0.0525036	intron-variant	RNF10	GRCh38.p7	12:120539850	GGAACTTTTTTTTTT[-/C]CCCTCAAGACAGTCT	9921
rs574520177	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120576142	GCCACCCCAGAGAAA[C/T]TGATGACGCCTGAAA	9921
rs574529886	snp	A/G	0.00438332	0.0466095	intron-variant	RNF10	GRCh38.p7	12:120547220	AAACAGTTTTAGAAG[A/G]TGCTTTAAAGACACC	9921
rs574576298	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120548685	TTTTTTTGAGATGGA[G/T]TCTCGCTCTGTCCCC	9921
rs574615125	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120554926	TTCTGCCTGGCCTTT[C/T]TATAGATGTTTCCCA	9921
rs574675566	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120568254	TCTCAAAAAAAAAAA[G/T]AAAAATACTGAGACA	9921
rs574691508	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120573979	AATGAATGCGAGAAT[A/G]GGTCTCCCATCCCCC	9921
rs574767737	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120542373	TGCCCAGGCTGGTCG[C/T]AAACTCGTGGACTCA	9921
rs574839563	snp	A/G	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120575331	CTTAACCAGAAAGTC[A/G]GAATTCCCAATTTGA	9921
rs574868093	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120569605	GGCACAAGGCACAAT[C/T]TCGGCTCACTGCAAC	9921
rs574963708	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120542641	CACTGCAACCTCTGC[C/G]TCCCGGGTTCAAATG	9921
rs575033306	snp	A/C/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120536683	CTTTTGGTCAGTGTT[A/C/G]GAACTGGTTTAGAGT	9921
rs575047285	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120536229	GAGTTTCACACCAGC[C/T]TGGGCAAGATAGTAA	9921
rs575088467	in-del	-/A	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120570888	AGCCAGCCTTTGTGG[-/A]AAAGTATAGCATTTC	9921
rs575192851	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120572105	ACGGAGTCTCCCTGT[C/T]CCCCAGGCTGGAGTT	9921
rs575245545	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120555876	TCACTGTAACCTCCA[C/T]CTCTTGGGTTCAAGC	9921
rs575280398	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120562883	TTCTAAGCCCTTGCC[C/T]TTCAAGCTAAGTGTG	9921
rs575305772	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120542510	TGACACTAACTGTTG[C/G]TAACTGAAGTAATAG	9921
rs575356705	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120556331	CGGGGTCAGGAGATC[A/G]AGACCATCCTGGCTA	9921
rs575722015	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120545831	GGCGTGAGCCATTGC[A/G]CCCAGCCCCCAGTAT	9921
rs575733120	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120545477	GATTACAGGCATGAG[C/T]CACCGCGCCTGGCCA	9921
rs575736634	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120544761	AATGGCTTTAATGAC[C/T]ATATTTTATCTGTCA	9921
rs575740022	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577551	AGGTGCATTAGAATG[C/T]GAAGGCAAATAGTTG	9921
rs575749769	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120553546	AGTAGCTGGGACTAC[A/G]GGCGCCCACCCCCTG	9921
rs575860109	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120539964	CCTCAGCCTCCTGAG[C/T]AGCTGGATTGCAGGT	9921
rs575880498	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120571616	GATGTTACTGTAGAC[G/T]TACCCAGGAAAGAGG	9921
rs575894293	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120557804	CATGTTCATATTAGT[C/T]ATAGGATTCCAGTAG	9921
rs575920336	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120570998	CTTCCTGTACCGGTC[A/G]CTGATTTCACTGGTG	9921
rs575994366	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120536307	CACACACCTGTAACC[C/T]TACCTACTTGGAAGG	9921
rs576457978	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120559984	GTGAGCCACCACACC[C/T]AGCTGGCTTGGTCTT	9921
rs576458441	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120553200	GTGATTTTTTTGCCT[C/T]AGCCTCCCGAATAGC	9921
rs576495391	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120559679	TGAGCCACCGTACTC[C/T]GCCTGGTGTTATTTT	9921
rs576796468	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120541298	AGTCTTGGATAATGA[G/T]GTTGGAGGATATGTG	9921
rs576797532	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120535065	TCGGGGACAGGCTCC[A/G]CTTTCTTTTATAGCT	9921
rs576832739	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120547394	CCTCCTGGGCTCAAG[G/T]GATCCTCCCACCTCA	9921
rs576864235	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120575102	AAATCCAAAAATTAG[C/T]CAGGCGGGTGCCTGT	9921
rs576888787	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120543493	ACATAGTGAGACCCC[C/T]GTCTGCACAAAAAAA	9921
rs576895715	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120574786	CAAAAATTAGCCGGG[C/T]GTGGTGGTGCATGCC	9921
rs576940814	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120541803	TGCAAACATAACTGA[C/T]TGAAACCTTGAACTC	9921
rs576948238	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120542733	AATGTTTGTATTTCT[A/C]GTAAAGATGGGGCTT	9921
rs577001198	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120568339	AATGTTCAAATGGGC[C/T]TTTAGCCTTCAAAAA	9921
rs577037685	snp	C/T	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120555150	AGTAGGCCTCAGCCT[C/T]GTGGCAGGGAGGCAC	9921
rs577063076	snp	A/C	1.64985e-05	0.0028721	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120560741	ATGAACAGCACAGCC[A/C]GTACTCCAAGTTGCT	9921
rs577070937	snp	A/C	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120536817	TGGGGCTCCTCTTTA[A/C]GCCACTAACATACAT	9921
rs577148922	snp	A/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120569650	TTGAAGCAATTCTTG[A/T]GCCTCAGCCTCCCGA	9921
rs577298125	snp	C/T	0.00597247	0.0543191	intron-variant	RNF10	GRCh38.p7	12:120535302	ACTCATCAGTCCACG[C/T]TCCTAAAACCACTAA	9921
rs577329493	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120576106	TAATACTCCATTTGG[C/T]ATGTCAGATAGGACC	9921
rs577332211	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120564617	TCAGAAAAAAAAAAT[G/T]GGGCTTCATTTTCTA	9921
rs577454143	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120569963	AGTGGTGCGATTTTG[A/G]CTCACTGCAACTTCC	9921
rs577642575	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120550466	GTTTGGGGCATTAAG[C/G]GTGGAAGACCGTTTG	9921
rs577697268	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120548883	CACCGTGTTAGCCAC[G/T]GTGGTCTCGATCTTC	9921
rs577740963	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120570615	GTCCAACACTGTTCA[C/G]GGCAGTGGATAGACT	9921
rs577808125	snp	C/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120550842	ACCTCGTGATCCGCC[C/T]GCCTCAGCCTCCCAA	9921
rs577850147	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120537607	CACTCCAGCCCGTCT[A/G]AAAAAACAAAAACTC	9921
rs577858984	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120562796	TTTCCCTCAAAGTTG[A/G]GATATTTAAGCACCT	9921
rs578016547	snp	C/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120544808	ATTTGACATAATCAC[C/G]TAAGCCTCTGTGTAA	9921
rs578039922	snp	C/T	1.64765e-05	0.00287019	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546491	TTTAACAACCAGTCC[C/T]GTCGCTCCAGTTCAC	9921
rs578070650	snp	A/G	0.00199481	0.0315187	intron-variant	RNF10	GRCh38.p7	12:120571693	CATTTGATAACTTGT[A/G]TACTGGATACTATTG	9921
rs578107627	snp	A/G	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120539121	TCAGCCACTATGGTA[A/G]GCATTTTACAGAAGT	9921
rs578254286	snp	G/T	0.000399281	0.0141238	intron-variant	RNF10	GRCh38.p7	12:120558900	AGTGTCCACAGAATT[G/T]TCGTTAATGAACATA	9921
rs745308694	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120575223	CCTGGGCAACAAGAG[C/T]TAAACTGTCTAAAAA	9921
rs745337476	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120544043	GACCAGCCTGGCCAA[A/T]GTGGCGAAACTCCAT	9921
rs745363300	in-del	-/A			intron-variant	RNF10	GRCh38.p7	12:120543177	ATTGTACTTACCAAG[-/A]AATAATTTTTTCTAA	9921
rs745364642	snp	C/T	3.29451e-05	0.00405851	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563892	CCTGGAGAGGAGCCC[C/T]GAGAAGATCTCAGCA	9921
rs745364827	snp	A/G	6.58979e-05	0.00573974	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575766	AAAAGAGTTGTTTCT[A/G]TAGTTTTAACACTGG	9921
rs745412599	in-del	-/A/AA			intron-variant	RNF10	GRCh38.p7	12:120556530	GTGAGACTCCGTCTC[-/A/AA]AAAAAAAAAAAAAAA	9921
rs745417589	snp	G/T	1.66123e-05	0.00288199	intron-variant	RNF10	GRCh38.p7	12:120565023	TAGGACCCCCTGCTT[G/T]CAGAGTTAGGCTTGC	9921
rs745419232	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120536044	GTGTTTTCAGCGACA[A/G]TGGGGATGTTGTGGC	9921
rs745440489	snp	A/G	2.0021e-05	0.00316388	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534935	CCCCGCTCCGCCTCG[A/G]CGGGGCCAGCCGGCG	9921
rs745498276	snp	C/G	1.64846e-05	0.0028709	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120560833	CAGCAGCTGGCAGAG[C/G]AGAAGCACACTCCCG	9921
rs745524503	snp	C/T	1.69758e-05	0.00291335	intron-variant	RNF10	GRCh38.p7	12:120560926	AAACCTTTTCACTTT[C/T]TCGGCGTTCTGTGGT	9921
rs745543597	snp	A/G	3.36553e-05	0.00410201	intron-variant	RNF10	GRCh38.p7	12:120546608	CGAGATGAGGTATGG[A/G]ATTTGAGAATGTCCT	9921
rs745562659	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120555166	GTGGCAGGGAGGCAC[A/T]TGAATGAGCCACACA	9921
rs745566182	in-del	-/CAG	1.64849e-05	0.00287092	cds-indel, nc-transcript-variant	RNF10	GRCh38.p7	12:120566955	CTCCATTTCTCCTCT[-/CAG]CAGAAGTCCAGGTTC	9921
rs745600077	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120550146	ATATATCTAAAATCT[A/G]AAAGTTTACCACGTG	9921
rs745662966	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120539057	GCTCTTGACAGGAAC[A/G]CTTTGGATTTATTAA	9921
rs745678324	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120550922	GTTATTTTTAAGCTT[C/G]GTTGTTAATATAAAA	9921
rs745702060	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120571826	TTTGAGAGGGGAAGA[-/T]TTGTCTTGGTTATAC	9921
rs745712610	snp	A/G	1.64795e-05	0.00287045	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120552520	GAGGCTCAACGGGCA[A/G]AGTTTAGCCCTGCCC	9921
rs745722908	snp	C/G	1.64773e-05	0.00287026	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563469	AGTGTCTGAACCAGA[C/G]CCTGAGGGGTTGCCA	9921
rs745749962	snp	A/G	1.65389e-05	0.00287562	intron-variant	RNF10	GRCh38.p7	12:120566989	CATGCAGGTAAACAG[A/G]TGAAATTTAATGAAT	9921
rs745803264	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120562576	ACCACACCTGGCCGT[A/G]TGTGTCTTTACAGTA	9921
rs745831090	snp	C/T	0.000150234	0.00866571	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563373	GTATCTGTCTGCCTT[C/T]GATGAAGAAACCACG	9921
rs745875981	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120572356	CAGGCATGAGCCACC[A/G]TGCCCGGCCATTGAC	9921
rs745922320	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120567862	GCATTTCATTATGGG[-/T]GTGTGTGTGTGTGTG	9921
rs745943960	snp	A/G	5.00079e-05	0.00500015	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563558	CTGAGTCCAGCCAGC[A/G]GGAACCCATCACCAA	9921
rs745988373	snp	C/T	1.64814e-05	0.00287061	missense, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575924	TCATGAAACTGGACA[C/T]ACCAGCTACTTCAGA	9921
rs745989392	snp	C/T	1.64779e-05	0.00287031	intron-variant	RNF10	GRCh38.p7	12:120557517	CTCTTCACTCCTTGC[C/T]CTGCTACATATGAGT	9921
rs746016406	snp	A/G	1.70038e-05	0.00291575	splice-acceptor-variant	RNF10	GRCh38.p7	12:120576589	CTGTGTCTCCCTTTA[A/G]AAGAGAAAGGAGGAA	9921
rs746062177	in-del	-/G			intron-variant	RNF10	GRCh38.p7	12:120556223	TTTTCTTTATGAGCA[-/G]GGGGCTTTTGACCTT	9921
rs746130262	snp	C/T			missense, synonymous-codon, nc-transcript-variant, intron-variant	RNF10	GRCh38.p7	12:120571248	GTCCCTCATTCTGCG[C/T]TGGGAGTCTGGAAGA	9921
rs746192822	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120547706	AGTAGGCTACCGTAA[A/G]TGGAGGAGGAGAGGT	9921
rs746201563	snp	C/G/T			intron-variant	RNF10	GRCh38.p7	12:120535314	ACGCTCCTAAAACCA[C/G/T]TAAGTTGTTCTACCC	9921
rs746222722	snp	C/T	1.69691e-05	0.00291278	intron-variant	RNF10	GRCh38.p7	12:120565397	CCATGTTGTCCTGGG[C/T]CTACCTCTTTACAAC	9921
rs746227302	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120536552	CCTGGTGTGAGACCA[C/T]TGGAGTATGGGTTCT	9921
rs746231878	in-del	-/AG	1.64741e-05	0.00286998	frameshift-variant, nc-transcript-variant	RNF10	GRCh38.p7	12:120557558	CAGTGTTGTTGCCAC[-/AG]AGTCACATCAGTATG	9921
rs746275913	snp	A/G	1.67203e-05	0.00289134	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120565491	AACGCCGCCGAGAGC[A/G]CAGGATTGAGATAGA	9921
rs746291640	snp	C/T			downstream-variant-500B	RNF10	GRCh38.p7	12:120577620	TTTTTAAGTTCATTA[C/T]AGGTAAGCTAGACAA	9921
rs746331062	snp	C/T	1.64738e-05	0.00286995	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563062	GAGTCTGTTTTTCAA[C/T]CCAGGAAGGTTAGTG	9921
rs746348709	snp	A/G	3.37923e-05	0.00411036	intron-variant	RNF10	GRCh38.p7	12:120552701	TTTTACAGGCCAAGT[A/G]AGTATTGCTACCCCT	9921
rs746378505	snp	A/C/G	3.30285e-05	0.00406366	intron-variant	RNF10	GRCh38.p7	12:120554692	ATCCTGACAGTCTAG[A/C/G]TTTTTCCTGTCTTTC	9921
rs746422047	snp	A/G			intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120576310	AAGAATCACATATGT[A/G]TGGCGTGCTATGTGC	9921
rs746452403	snp	C/T	0.00110223	0.02345	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577279	AGGAGGGTTTTGCCT[C/T]TTCTTGAGCATGGCT	9921
rs746454365	snp	A/G/T	1.64844e-05	0.00287087	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563486	CTGAGGGGTTGCCAG[A/G/T]GGCCTGTGATGACTT	9921
rs746510909	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120563127	TGCTGTCATTGAGCT[G/T]GTAGGCATTACTGTG	9921
rs746609961	snp	C/G	4.94205e-05	0.0049707	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120552544	CCTGCCCAGTTCTCT[C/G]GTCCTAAGAAGATCA	9921
rs746663122	snp	A/G	0.000378941	0.0137596	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120552648	TAGCTGGGGAAAGAG[A/G]AACAAGTGGGGACAT	9921
rs746664072	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120544213	GCCTGGGCAATAGAG[C/T]GAGACTGTTAAAAAC	9921
rs746681452	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120576384	TACCTCACGTTACAG[A/G]TGGGGAAACTGAGGT	9921
rs746773965	snp	C/T	0.000115311	0.00759224	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120552605	AACCCCGTGGCCAGA[C/T]GGGTCACTTTGAAGG	9921
rs746790612	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120569850	GCCTATCTGTGATAC[C/T]GAGATTGTGTTTTCA	9921
rs746792671	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120542006	TGAGTAGCTGGGACT[A/G]CAGGCTCCCGCCACC	9921
rs746803228	snp	C/G	1.65669e-05	0.00287805	intron-variant	RNF10	GRCh38.p7	12:120571144	CTCTTGTTAAGGACA[C/G]CCCTTGGAACGTGAC	9921
rs746826819	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120540796	AACTGTTTCCTTGCC[A/G]GTGTGGTAATAAGTG	9921
rs746846154	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120544051	TGGCCAATGTGGCGA[A/C]ACTCCATCTCTACTA	9921
rs746856077	snp	C/T	0.000362396	0.0134561	synonymous-codon, missense, nc-transcript-variant, intron-variant	RNF10	GRCh38.p7	12:120571237	CAGTCAGGGCAGTCC[C/T]TCATTCTGCGTTGGG	9921
rs746858092	snp	C/G	3.34616e-05	0.00409019	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563564	CCAGCCAGCAGGAAC[C/G]CATCACCAAGTCAGG	9921
rs746897284	in-del	-/CCGCCT	2.82115e-05	0.00375566	cds-indel, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534842	CCAACGCCGCCGCCA[-/CCGCCT]CCGCCTCCGACATGG	9921
rs746913283	snp	C/G	1.87633e-05	0.00306289	intron-variant	RNF10	GRCh38.p7	12:120563668	GCCGCAGAGGTGTTT[C/G]AGAGGTGACCCGGTG	9921
rs746932652	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120564805	AAAAAATCAGAAACA[A/G]CTGATGGGCTTTAGA	9921
rs746982813	snp	A/G	1.64757e-05	0.00287012	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120557636	GGTGTTGGTGGCTTT[A/G]CCCAAATCCAAATGG	9921
rs747030851	snp	C/T	1.64803e-05	0.00287052	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120546454	TCGCAAACGTGAACT[C/T]TCCTACCCCAAAAAT	9921
rs747083327	snp	C/T	3.30077e-05	0.00406236	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576718	TGTTTTTGTTTTTTT[C/T]TCCCCCATGCTTTTG	9921
rs747136612	snp	A/G	3.35576e-05	0.00409606	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120565500	GAGAGCGCAGGATTG[A/G]GATAGAGGAGAACAA	9921
rs747175463	snp	A/G	1.64765e-05	0.00287019	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546483	ATGAAAGTTTTAACA[A/G]CCAGTCCCGTCGCTC	9921
rs747177102	snp	C/T	3.29804e-05	0.00406068	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546431	TCCAGTGGATCCAAG[C/T]GTTATAATCGCAAAC	9921
rs747226884	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120573768	GCCGTTTTAAACAAC[C/T]GTGTTCCTGTGCCCA	9921
rs747339834	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120537652	TGTTAGATTTTACAA[A/G]TAACACATATGTGCC	9921
rs747364566	snp	A/G	1.64741e-05	0.00286998	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563070	TTTTCAACCCAGGAA[A/G]GTTAGTGTGTTCCTG	9921
rs747389756	snp	A/T	1.66624e-05	0.00288633	intron-variant	RNF10	GRCh38.p7	12:120566774	CTCAAAAAAAAAAAA[A/T]AAAAATTGAATTCTG	9921
rs747411433	snp	C/T	1.64936e-05	0.00287168	intron-variant	RNF10	GRCh38.p7	12:120554705	AGCTTTTTCCTGTCT[C/T]TCCTATTTCTAGCTG	9921
rs747463113	snp	A/G	3.29712e-05	0.00406011	intron-variant	RNF10	GRCh38.p7	12:120554825	TGAGTAGCTCAGCCA[A/G]GCCCATAAGCTATGA	9921
rs747471809	snp	A/G	5.64215e-05	0.00531108	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534842	CCCAACGCCGCCGCC[A/G]CCGCCTCCGACATGG	9921
rs747489482	in-del	-/C	1.64806e-05	0.00287054	frameshift-variant, nc-transcript-variant, intron-variant	RNF10	GRCh38.p7	12:120571196	TCCCTTTCAGACTTT[-/C]TGCTGACCCCTCTGT	9921
rs747572561	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120536661	AAAAGATAGAAGGTA[A/G]CCAGTCCTTTTGGTC	9921
rs747607438	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120551725	TGCAACCTTGAATTC[A/C]TGGGCTCAAGTGCCC	9921
rs747640372	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120566171	CAAGTGTATACTTGG[A/G]GTCCCAACACCGTGT	9921
rs747649450	in-del	-/GACTGCCCCTGCTGCTGGGGA	3.03725e-05	0.00389684	intron-variant	RNF10	GRCh38.p7	12:120535001	GCAGTGGGCGGGGGC[-/GACTGCCCCTGCTGCTGGGGA]GAGTCGTTGCTCTCA	9921
rs747701120	snp	C/T	1.6623e-05	0.00288292	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120552686	TTAACAAGGAACTCT[C/T]TTTACAGGCCAAGTG	9921
rs747710537	in-del	-/TTTGGAGAGAATGACATC			intron-variant	RNF10	GRCh38.p7	12:120543000	TTTTAGGTGGTCAGG[-/TTTGGAGAGAATGACATC]TTTGGAGAGAATGAC	9921
rs747731001	snp	A/C			utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577457	CCACCATCTCCCTCT[A/C]ATCTAGAGCAGTTTT	9921
rs747755891	snp	A/G	1.87556e-05	0.00306226	intron-variant	RNF10	GRCh38.p7	12:120552744	AAAGTAGGACTCTCC[A/G]GATAGCTGTGGTGCC	9921
rs747772965	snp	A/G	1.64765e-05	0.00287019	missense, synonymous-codon, nc-transcript-variant, intron-variant	RNF10	GRCh38.p7	12:120571263	TTGGGAGTCTGGAAG[A/G]AGACTCTCCCTTCCC	9921
rs747790148	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120565290	GAACTGTATCATGAG[C/T]CTTAGTACCTCCTAA	9921
rs747816690	in-del	-/AAAAA			intron-variant	RNF10	GRCh38.p7	12:120540081	TCATGAGGAACTTAA[-/AAAAA]AAAAAAATAGGGGTG	9921
rs747873640	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120573937	ACTGGGATCCAGTGG[C/T]AGACATCACTCATCA	9921
rs747909551	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120542446	GGCATGAGCCACCAA[A/G]TCCAGCGCTGAAACT	9921
rs747984548	snp	A/G	4.94173e-05	0.00497053	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563860	AATGTGCGCTGCCTC[A/G]TGCGGGAGTACGGCA	9921
rs747988858	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120541559	CCTGCCTCAGCCTCC[C/T]GAGCAGCTGGGACTA	9921
rs748014859	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120539269	ATGAAGTCCTAGGCG[G/T]TATTTTTCAATAAGC	9921
rs748037746	snp	C/T	0.000266245	0.0115348	intron-variant	RNF10	GRCh38.p7	12:120560695	GAGCTTTGAATGTTG[C/T]ATTTCTTTGATCTTG	9921
rs748040908	snp	A/G	0.000253389	0.011253	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577269	CATGTGTGAAAGGAG[A/G]GTTTTGCCTCTTCTT	9921
rs748095559	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120552768	TGGTGCCTCTGTGAG[A/T]GGCTTTTTTTAAGCT	9921
rs748107231	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120572611	TTGTTTTGTTTTGTT[A/T]TGAGTTGAAGTCTTG	9921
rs748131170	snp	C/T	1.64765e-05	0.00287019	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546494	AACAACCAGTCCCGT[C/T]GCTCCAGTTCACAGA	9921
rs748147007	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120540979	TCCTGCCTCAGCCCC[C/T]GGAGTAGCTGGGATT	9921
rs748181315	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120537821	CATGCTTCTTCACTA[A/G]CCATAATCCACTGCT	9921
rs748226473	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120573049	ACTATTTTGCTGTTA[C/T]ATATTTGCTTTCTCT	9921
rs748230146	in-del	-/AAA			intron-variant	RNF10	GRCh38.p7	12:120567701	GCGAGACTTTGTCTC[-/AAA]AAAAAAAAAAAAAAA	9921
rs748238798	snp	A/G	1.7403e-05	0.00294978	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120565526	AACAAGAAACAGGGC[A/G]AGTGTAAGTTCAGGA	9921
rs748244710	snp	G/T	1.65641e-05	0.00287781	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120546577	ACTCTTTAGCTCTTC[G/T]TTTAATGGTGGAAGA	9921
rs748257842	in-del	-/TTGTT			intron-variant	RNF10	GRCh38.p7	12:120568966	ATTTCTCAGGCATTC[-/TTGTT]TTGTTTTGTTTTGTT	9921
rs748330445	snp	A/G	1.64969e-05	0.00287196	intron-variant	RNF10	GRCh38.p7	12:120554843	CCATAAGCTATGAAT[A/G]GGAGCACTAAATAAA	9921
rs748411720	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120562344	CAGTGGCGTGATCTC[A/G]GCTCATCACAACCTC	9921
rs748417076	snp	A/T	1.6483e-05	0.00287076	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563418	GGACACTCCTTCTAG[A/T]CCTCTTGCTCTCCCT	9921
rs748568698	snp	C/T	1.64743e-05	0.00287	synonymous-codon, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575799	TTTTTTAGATGAGAA[C/T]AGCTTAGTTCCTCCT	9921
rs748579098	snp	A/G	2.18878e-05	0.00330809	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534851	GCCGCCACCGCCTCC[A/G]ACATGGACAAGAACA	9921
rs748591628	in-del	-/ATATT			intron-variant	RNF10	GRCh38.p7	12:120545149	TTCAGAATTGAACAC[-/ATATT]ATAATTGAAGAGAAA	9921
rs748600889	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120570585	GCTGCTGGGGGAGAG[A/C]ATAGGGCCCCTCTCG	9921
rs748613259	snp	C/T	4.94222e-05	0.00497078	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557351	GCAGCCAAGATAACC[C/T]GTTGTGGACACATCT	9921
rs748625894	snp	G/T	8.27767e-05	0.00643284	intron-variant	RNF10	GRCh38.p7	12:120565058	GTTGAGTATTGGTCC[G/T]TTTTCCAATGTAGGA	9921
rs748630500	snp	G/T	5.99862e-05	0.00547627	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534939	GCTCCGCCTCGGCGG[G/T]GCCAGCCGGCGAGTC	9921
rs748746413	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120538882	GTAATCTGCCTTGAA[G/T]AATGCCTCTGAGCTG	9921
rs748758109	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120541333	CTTTATATACCTATC[A/C]TCGTAGAATCTCCTT	9921
rs748818916	snp	G/T	1.88831e-05	0.00307265	utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534764	TGAGCCTGGGTCCCC[G/T]CCGCGCCCGCTCCGC	9921
rs748825593	snp	C/G	1.64732e-05	0.0028699	splice-donor-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575689	CTGCTCCAAAGAAAG[C/G]TGAGGATGGTCCACT	9921
rs748876290	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120566306	TGTAATTAACCTGCA[C/T]GTTTGTTACCCAGCC	9921
rs748924190	in-del	-/AGTT	0.000115366	0.00759405	intron-variant	RNF10	GRCh38.p7	12:120557488	TTGAGACATTTACTC[-/AGTT]AGATCCCAATCTCTT	9921
rs748929472	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120552832	CGTTCTTTTTCTGTT[C/T]ACCACTGCCCCGCCC	9921
rs748937368	in-del	-/C	0.000187038	0.00966872	intron-variant	RNF10	GRCh38.p7	12:120539343	GCATCATTCCTGATA[-/C]CACCTCTCTCTTCCT	9921
rs748950886	snp	A/T	4.25035e-05	0.00460976	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534830	CCGCTGAGCTCCCCC[A/T]ACGCCGCCGCCACCG	9921
rs749039206	in-del	-/AA			intron-variant	RNF10	GRCh38.p7	12:120567702	CGAGACTTTGTCTCA[-/AA]AAAAAAAAAAAAAAA	9921
rs749074675	snp	C/T	1.64844e-05	0.00287087	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120560828	TAGAGCAGCAGCTGG[C/T]AGAGGAGAAGCACAC	9921
rs749094770	snp	C/T	1.65954e-05	0.00288053	intron-variant	RNF10	GRCh38.p7	12:120560708	TGCATTTCTTTGATC[C/T]TGCTGGCATTCTTAT	9921
rs749122189	snp	C/T	1.648e-05	0.0028705	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120546526	AAGCAAGACTTTTAA[C/T]AAGATGCCTCCTCAA	9921
rs749156853	in-del	-/TTTTG			intron-variant	RNF10	GRCh38.p7	12:120569890	TTTCTGAAAGCTGCT[-/TTTTG]TTTTGTTTTGTTTTG	9921
rs749177719	snp	C/T	1.64871e-05	0.00287111	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120566828	TTTCCTTTGCAGACC[C/T]AGAAGTCCACATTCC	9921
rs749286782	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120538919	GACCTGGAGATTTTA[A/T]TGGCTTTGAAAATTG	9921
rs749374259	snp	C/T	1.71029e-05	0.00292424	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563349	TTTGCTGCAACAGGG[C/T]GTGCTGGAGTATCTG	9921
rs749381533	snp	C/G/T	3.29534e-05	0.00405904	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120566900	CCTGCTCCTCTGATT[C/G/T]TGCTTTGGGTCCCAC	9921
rs749425704	snp	A/G	1.64762e-05	0.00287016	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563445	CCCTCTGGTAGAAGA[A/G]GAGGAAGCAGTGTCT	9921
rs749468403	snp	A/G	8.2373e-05	0.00641714	intron-variant	RNF10	GRCh38.p7	12:120563074	CAACCCAGGAAGGTT[A/G]GTGTGTTCCTGTTAC	9921
rs749480552	snp	A/T	1.65957e-05	0.00288055	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563548	ACCATTTGCACTGAG[A/T]CCAGCCAGCAGGAAC	9921
rs749505550	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120563193	AGTATTTTCTGTATG[C/T]TTGTTATTAGTTCTT	9921
rs749505824	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120548961	AGGCATGAGCCACCG[C/T]GCCCGGCTGAGGGAT	9921
rs749523880	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120545975	GGCCTAGGACAACCC[C/T]TTGTAGTATAGAATC	9921
rs749536096	snp	C/G	1.64789e-05	0.0028704	intron-variant	RNF10	GRCh38.p7	12:120557512	CCAATCTCTTCACTC[C/G]TTGCCCTGCTACATA	9921
rs749563997	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120559749	TGCCCAGGCTGGAGT[A/G]CAATGGTGCGATCTT	9921
rs749600825	snp	C/G			synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120552594	TTTCACTTTTGAACC[C/G]CGTGGCCAGACGGGT	9921
rs749612496	in-del	-/G			intron-variant	RNF10	GRCh38.p7	12:120555796	CATCGTACCTGGCCT[-/G]CTTTTTTTTTTTGAG	9921
rs749650943	snp	C/G	1.64779e-05	0.00287031	missense, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575906	AAGCTATTGAAGCAG[C/G]CTTCATGAAACTGGA	9921
rs749656896	snp	C/T			upstream-variant-2KB	RNF10	GRCh38.p7	12:120533042	GTGCACTGGCACGAT[C/T]GTATCTCACTGCAAC	9921
rs749690593	snp	G/T	5.10417e-05	0.00505156	intron-variant	RNF10	GRCh38.p7	12:120565389	GGTAATGACCATGTT[G/T]TCCTGGGTCTACCTC	9921
rs749704155	in-del	-/TTTTTAT			intron-variant	RNF10	GRCh38.p7	12:120545179	GAAAAACAAGAAACA[-/TTTTTAT]TTTTTATTTTTTATT	9921
rs749887354	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120556637	AAGTTTTATTAAAAA[A/G]AAATGAAGTCTTTTT	9921
rs749991782	snp	A/G	1.64784e-05	0.00287035	intron-variant	RNF10	GRCh38.p7	12:120557472	ATCTCAAGAGGTGAG[A/G]TTGAGACATTTACTC	9921
rs750003149	snp	A/G/T	4.94192e-05	0.00497067	missense, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575855	GTGATAATTCAGACC[A/G/T]TGTTCCTGTGCCCAG	9921
rs750004265	snp	C/T	3.30792e-05	0.00406675	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575989	CAGGGTTGTCAAACA[C/T]ACTACACATGTACTG	9921
rs750031822	in-del	-/G			intron-variant	RNF10	GRCh38.p7	12:120550289	AAGCTAATTGGAAGA[-/G]GAGGAGGTCAAGGAC	9921
rs750046793	snp	G/T	1.68912e-05	0.00290608	intron-variant	RNF10	GRCh38.p7	12:120534985	TAAGGACGGGCCTGC[G/T]GCAGTGGGCGGGGGC	9921
rs750049681	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120566646	ACGTGCCTGTGGTCC[C/T]GGCTACTCGGGAGGC	9921
rs750058332	snp	C/T	3.29468e-05	0.00405861	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120565131	CTGTGAGTTCAGCAT[C/T]TGTGAACTGGCTTTG	9921
rs750098273	snp	C/T	1.70185e-05	0.00291701	intron-variant	RNF10	GRCh38.p7	12:120546369	AAGTGAATGTATCAG[C/T]TTCTTAAGACGTTCT	9921
rs750107069	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120568673	TAGAGACAGGGTCTC[A/T]CCATGTTGGCCAGGC	9921
rs750117345	snp	A/G	3.3077e-05	0.00406662	intron-variant	RNF10	GRCh38.p7	12:120565225	CTTCTCTTTATAGTA[A/G]GGTTCAGGGATTCTT	9921
rs750168666	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120539571	GAACTAGAGCTAGAA[A/G]TGAAGATGCCAAGTA	9921
rs750183269	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120564625	AAAAAATTGGGCTTC[A/G]TTTTCTACTATTTCA	9921
rs750311424	snp	G/T	1.66261e-05	0.00288319	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120565466	CAGCGCCAAAAGAAG[G/T]CTCGGGAGGAACGCC	9921
rs750348941	snp	C/T	1.64751e-05	0.00287007	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120552630	TGAAGGCAGTGGACA[C/T]GGTAGCTGGGGAAAG	9921
rs750357392	snp	A/G	1.76148e-05	0.00296767	intron-variant	RNF10	GRCh38.p7	12:120552726	ACCCCTCAGAGGAAA[A/G]GGAAAGTAGGACTCT	9921
rs750364829	snp	C/T	1.64735e-05	0.00286993	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563026	CTGGAACAACTGGTG[C/T]TGATGGCTCCCTTGG	9921
rs750426110	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577063	AGGGCTTCCTGGACT[C/T]AGTACACCTCTCAGT	9921
rs750459502	snp	G/T	1.64762e-05	0.00287016	missense, nc-transcript-variant, intron-variant	RNF10	GRCh38.p7	12:120571224	TGTCACCCACTGCCA[G/T]TCAGGGCAGTCCCTC	9921
rs750476706	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120553539	CCTCCCGAGTAGCTG[G/T]GACTACAGGCGCCCA	9921
rs750512359	snp	C/T	3.73748e-05	0.00432273	intron-variant	RNF10	GRCh38.p7	12:120563655	AGAGGGCTGGGTTGC[C/T]GCAGAGGTGTTTCAG	9921
rs750519209	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120542237	GCCATCATAGCACAC[C/T]GCAGCCTCAACCTTG	9921
rs750558134	snp	A/G	0.00111421	0.0235767	intron-variant, utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120574499	TGGTTGGATCTGAAA[A/G]TTAATGATGAAGGAG	9921
rs750611679	snp	C/T	1.6476e-05	0.00287014	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563828	AAGATGGACAGCATA[C/T]GTTCCTGCACCCTGT	9921
rs750700301	in-del	-/C	1.64874e-05	0.00287113	frameshift-variant, nc-transcript-variant	RNF10	GRCh38.p7	12:120563414	CTCTGGACACTCCTT[-/C]TAGACCTCTTGCTCT	9921
rs750795022	snp	G/T	0.000593697	0.0172191	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576705	TCCATCTGGTTTTTG[G/T]TTTTGTTTTTTTTTC	9921
rs750824600	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120548553	GGAGGATGGGAAGAA[C/G]AAACAGCAAATTTAC	9921
rs750834461	in-del	-/C			intron-variant	RNF10	GRCh38.p7	12:120568090	TCTCTACAAAAAATA[-/C]GAAATTTAGCCAGGT	9921
rs750877950	snp	C/T	1.64868e-05	0.00287109	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120560762	CCAAGTTGCTGCTGG[C/T]CTCTAAGGAGCAGGT	9921
rs750886587	snp	C/T	0.000102219	0.00714837	intron-variant	RNF10	GRCh38.p7	12:120565570	ACTAGCACTGCTGTA[C/T]GTCGTTGTATAGAAC	9921
rs750906052	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120553957	TCGCCCAGGCTGGAG[C/T]GTAGTGGCGTGATCT	9921
rs750935728	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120573252	CATTTGTCTCAGCGT[C/T]CTTCATTTTCAACTC	9921
rs751013829	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120560538	CTCTGGGTTTCTTAG[A/G]TTTCTTATATCAAGA	9921
rs751071405	snp	A/G	3.866e-05	0.00439642	intron-variant	RNF10	GRCh38.p7	12:120576551	AGGGGACAAGGGATG[A/G]CATTTTAAGTTAAGC	9921
rs751081133	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120547227	TTTAGAAGGTGCTTT[A/G]AAGACACCTTCTCTG	9921
rs751120719	snp	G/T	1.65468e-05	0.00287631	intron-variant	RNF10	GRCh38.p7	12:120565234	ATAGTAGGGTTCAGG[G/T]ATTCTTGTGGCTAGA	9921
rs751224475	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120571885	GCTGGGTGGGGGAAC[A/G]ATAGGCTAGTGAGGC	9921
rs751262497	snp	C/T	1.6473e-05	0.00286988	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563030	AACAACTGGTGCTGA[C/T]GGCTCCCTTGGCGAA	9921
rs751273181	in-del	-/GTGAGCTG			intron-variant	RNF10	GRCh38.p7	12:120564567	GAGATCAAGTCTGCA[-/GTGAGCTG]GCCTGGGCGGCAGAG	9921
rs751352713	snp	C/T	4.94401e-05	0.00497168	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120566912	ATTCTGCTTTGGGTC[C/T]CACCAGCACCGAGGG	9921
rs751357131	in-del	-/CAAGTG	1.64757e-05	0.00287012	cds-indel, nc-transcript-variant	RNF10	GRCh38.p7	12:120554777	TGCTGATCCTGATAC[-/CAAGTG]ATTAGTTAACTGGGA	9921
rs751447105	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120574301	TGAACCCCATGGGGT[G/T]TGTCTCTTGATATTT	9921
rs751458516	snp	C/G	1.83353e-05	0.00302776	intron-variant	RNF10	GRCh38.p7	12:120552740	AGGGAAAGTAGGACT[C/G]TCCGGATAGCTGTGG	9921
rs751463202	snp	C/T	1.64751e-05	0.00287007	intron-variant	RNF10	GRCh38.p7	12:120575624	CACTTCTTTCCCACT[C/T]TGGCAGATGCTGAGG	9921
rs751466881	snp	C/T	1.64795e-05	0.00287045	intron-variant	RNF10	GRCh38.p7	12:120563115	CCGTTCCTCAAATGC[C/T]GTCATTGAGCTGGTA	9921
rs751484804	snp	C/G	5.81277e-05	0.00539078	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534818	CCCCCGTTGATGCCG[C/G]TGAGCTCCCCCAACG	9921
rs751512291	snp	A/G	1.64735e-05	0.00286993	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563852	ACCCTGTGAATGTGC[A/G]CTGCCTCGTGCGGGA	9921
rs751514446	snp	A/G	1.64751e-05	0.00287007	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575732	GTTTGGCTTCTTTCC[A/G]TAAAAGGCTGTTTCT	9921
rs751522013	snp	C/T	1.64749e-05	0.00287005	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120554751	TGAAGACCAAGACTA[C/T]ACAGCTCATTTTGCT	9921
rs751555609	snp	A/G	0.000115313	0.0075923	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120552611	GTGGCCAGACGGGTC[A/G]CTTTGAAGGCAGTGG	9921
rs751563596	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120536275	AAGAAAAAAAAAAAA[C/T]TAGCCGAGTGTGGTG	9921
rs751590250	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120565965	TTGGATTTAAGAGAT[A/C]TTTCGTAGCAGTAAG	9921
rs751601376	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120574572	GCGGTGTCAGGAGAG[A/G]GTTTAGTTAGTTTTC	9921
rs751658901	snp	A/C	1.66446e-05	0.00288479	intron-variant	RNF10	GRCh38.p7	12:120560688	CCATCGTGAGCTTTG[A/C]ATGTTGCATTTCTTT	9921
rs751695158	in-del	-/CT			intron-variant	RNF10	GRCh38.p7	12:120535834	AGGTGAAGTTTTTAC[-/CT]CTGTTTTCACTGTGC	9921
rs751707080	snp	A/G	1.64825e-05	0.00287071	intron-variant	RNF10	GRCh38.p7	12:120563957	AGGTGAGGCCTTCCT[A/G]TAGAAATGGAGGGTC	9921
rs751785103	snp	A/G	4.94499e-05	0.00497217	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120560786	AGCAGGTGCTGCACC[A/G]GGTAGTTCTGGAGGA	9921
rs751787672	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120542362	TCTTGCTATGTTGCC[C/G]AGGCTGGTCGCAAAC	9921
rs751913257	snp	C/T	1.6476e-05	0.00287014	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120566883	TGCCTTCAATTCTTA[C/T]ACCTGCTCCTCTGAT	9921
rs751932993	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120549575	GGATCTCCTGAGGCC[A/C]GGAGTTTGAGACGGG	9921
rs751935548	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120566256	TTTTTTGTTTTCACC[-/T]TTTTATTATGGAAAT	9921
rs751945365	in-del	-/AA	1.64757e-05	0.00287012	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575750	AAAGGCTGTTTCTAG[-/AA]AAAGAGTTGTTTCTA	9921
rs751988016	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120538678	AGAGAGAAGGTAGGC[A/C]GTTTATGGGCAGGCA	9921
rs752059239	snp	A/T			missense, utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120575664	GCAAAAGCAGATGTG[A/T]GGCCCAAAACTGCTC	9921
rs752063427	snp	A/C/G	3.29512e-05	0.00405891	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557333	TGCCTCTATCCACCT[A/C/G]CTGCAGCCAAGATAA	9921
rs752165813	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120548799	GAGTAGCTGGGACTA[C/T]AGCTGGGACTATTAG	9921
rs752189774	snp	A/G	1.66701e-05	0.002887	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120565482	CTCGGGAGGAACGCC[A/G]CCGAGAGCGCAGGAT	9921
rs752224502	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120537365	GGTGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	9921
rs752240070	snp	A/G	5.36687e-05	0.00517991	intron-variant	RNF10	GRCh38.p7	12:120563290	GTCTGCATTTGCCAC[A/G]TTGCTTTCGGAAAGC	9921
rs752289695	snp	A/G	6.58924e-05	0.0057395	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563048	CTCCCTTGGCGAAGG[A/G]GTCTGTTTTTCAACC	9921
rs752299282	snp	A/G	1.6476e-05	0.00287014	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120554778	TGCTGATCCTGATAC[A/G]TTAGTTAACTGGGAC	9921
rs752497084	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120554643	TGATTTCTAAGTGAA[G/T]AGATGACAATTTCTG	9921
rs752534210	snp	C/T	0.000131778	0.00811614	synonymous-codon, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575832	CCCTGTGGACAGCGA[C/T]GGGGAGAGTGATAAT	9921
rs752569216	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120567127	GAGGTACATCAAATT[C/G]TTTTATTCATCTTTC	9921
rs752583784	snp	G/T	1.64757e-05	0.00287012	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575742	TTTCCATAAAAGGCT[G/T]TTTCTAGAAAAAGAG	9921
rs752588724	snp	A/G	1.64879e-05	0.00287118	intron-variant	RNF10	GRCh38.p7	12:120563974	AGAAATGGAGGGTCA[A/G]GCAGCAGTATTAACC	9921
rs752589483	snp	A/G	1.64825e-05	0.00287071	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120565088	ATGTTCGACAGCGTC[A/G]CAGATATCTCTCTCA	9921
rs752598449	snp	C/T	3.33217e-05	0.00408163	intron-variant	RNF10	GRCh38.p7	12:120557273	CCTTCTGGTGGCATT[C/T]TGTTTCAGCGCATTT	9921
rs752601268	snp	A/C	4.60925e-05	0.00480043	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534827	ATGCCGCTGAGCTCC[A/C]CCAACGCCGCCGCCA	9921
rs752622272	in-del	-/CAT	1.64735e-05	0.00286993	cds-indel, nc-transcript-variant	RNF10	GRCh38.p7	12:120557362	AACCCGTTGTGGACA[-/CAT]CTTCTGCTGGGCATG	9921
rs752637201	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120569355	TGTGGTGACCATTTT[A/G]TTCATATGCATATCA	9921
rs752643444	in-del	-/G	1.81109e-05	0.00300917	intron-variant	RNF10	GRCh38.p7	12:120563627	CTTTTACCAAGGTGA[-/G]GGGTGCCGGAAGAGA	9921
rs752643854	snp	A/G	1.64819e-05	0.00287066	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120560811	GGAGGAGAAAGTAGC[A/G]CTAGAGCAGCAGCTG	9921
rs752652612	snp	A/C	1.92298e-05	0.00310073	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534882	GCGGCTCCAACAGCT[A/C]CTCCGCCTCTTCGGG	9921
rs752727743	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120563138	AGCTGGTAGGCATTA[C/G]TGTGAGATCTAAACC	9921
rs752728188	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120553689	ATTACAGGCGTGAGC[C/T]ACGGCACCCAACCAG	9921
rs752729407	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576833	AGAAAATTTTAAATA[C/T]AGTGTATTTTCCAGC	9921
rs752806246	in-del	-/T			utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576984	TAAGATTGAGTCCCC[-/T]TTGAGATGCATTAGA	9921
rs752829169	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120549685	AGTTACTTGGGAGGC[A/T]GAGGCAGGAGAATTG	9921
rs752839772	snp	A/G	1.66101e-05	0.0028818	intron-variant	RNF10	GRCh38.p7	12:120560893	GAGCTCAAGGTGAGA[A/G]GATGCATTGGAGATG	9921
rs752867300	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120575067	AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAA	9921
rs752943660	snp	A/G	1.65433e-05	0.002876	intron-variant	RNF10	GRCh38.p7	12:120552488	TACTGATTCATTCTC[A/G]TTCTCTCTAGGTAGC	9921
rs752949273	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120570721	TGCATCCTTGTGCTG[A/G]ATCTTGTTGATGTGT	9921
rs752950320	snp	C/G	1.64738e-05	0.00286995	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120552600	TTTTGAACCCCGTGG[C/G]CAGACGGGTCACTTT	9921
rs752952458	snp	C/T	3.29468e-05	0.00405861	missense, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575818	TTAGTTCCTCCTGCC[C/T]CTGTGGACAGCGACG	9921
rs753030792	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120544665	TGTCTCTAAATAAAT[A/G]AAGTGCATAAGTAAT	9921
rs753043189	snp	A/G	1.65064e-05	0.00287279	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563515	TTGGAGTTAGCAGAT[A/G]ACAATCTTAAAGAGG	9921
rs753096104	snp	C/T	1.64909e-05	0.00287144	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120566966	CTCTCAGCAGAAGTC[C/T]AGGTTCCCATGCAGG	9921
rs753096569	snp	A/G	1.64784e-05	0.00287035	intron-variant	RNF10	GRCh38.p7	12:120557500	CTCAGTTAGATCCCA[A/G]TCTCTTCACTCCTTG	9921
rs753130041	in-del	-/ATTTT			intron-variant	RNF10	GRCh38.p7	12:120559701	TGTTATTTTTTTTTA[-/ATTTT]ATTTTTTGAGGCAGA	9921
rs753199233	snp	C/T	1.77385e-05	0.00297808	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563613	CTCTCCTTGTTACTA[C/T]TTTTACCAAGGTGAG	9921
rs753209706	snp	A/G	6.33734e-05	0.00562874	intron-variant	RNF10	GRCh38.p7	12:120535001	GCAGTGGGCGGGGGC[A/G]ACTGCCCCTGCTGCT	9921
rs753250531	snp	A/G	3.29473e-05	0.00405864	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557566	TTGCCACAGAGTCAC[A/G]TCAGTATGTTGTTGG	9921
rs753290938	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120554932	CTGGCCTTTCTATAG[A/C]TGTTTCCCAGAGGTC	9921
rs753296585	in-del	-/GAG	1.68151e-05	0.00289953	cds-indel, nc-transcript-variant	RNF10	GRCh38.p7	12:120565505	CGCAGGATTGAGATA[-/GAG]GAGAACAAGAAACAG	9921
rs753360132	in-del	-/TTAGA			intron-variant	RNF10	GRCh38.p7	12:120568987	TTGTTTTGTTTTGTT[-/TTAGA]TGGAGTTTCGCTCTT	9921
rs753416889	snp	C/T	4.96545e-05	0.00498245	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563387	TCGATGAAGAAACCA[C/T]GGAAGTTTGTTCTCT	9921
rs753473815	snp	G/T	1.64751e-05	0.00287007	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575755	CTGTTTCTAGAAAAA[G/T]AGTTGTTTCTATAGT	9921
rs753555873	snp	C/T	1.64751e-05	0.00287007	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120557443	CATCTGTTACAGTTC[C/T]GTGCATAAGAAGGAT	9921
rs753577810	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120545150	TCAGAATTGAACACA[C/T]ATTATAATTGAAGAG	9921
rs753588470	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120537516	ACCTGTAATCCCAGC[C/T]ACTCGGGGGGCTGAG	9921
rs753606434	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120549424	TGCAGGGCTGATGTG[G/T]AATAGGAAAAGAGTT	9921
rs753607127	snp	C/T	2.36516e-05	0.00343878	intron-variant	RNF10	GRCh38.p7	12:120534976	CAAGAGCGGTAAGGA[C/T]GGGCCTGCGGCAGTG	9921
rs753614943	snp	A/G			intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120576013	TGTACTGCCATTCCC[A/G]CCTGGATTCAGTGGC	9921
rs753666425	snp	C/T	4.95675e-05	0.00497808	intron-variant	RNF10	GRCh38.p7	12:120565214	CCCCTGCTCTGCTTC[C/T]CTTTATAGTAGGGTT	9921
rs753670946	snp	G/T	1.64732e-05	0.0028699	missense, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575840	ACAGCGACGGGGAGA[G/T]TGATAATTCAGACCG	9921
rs753719530	snp	C/T	3.29451e-05	0.00405851	intron-variant	RNF10	GRCh38.p7	12:120562939	TGTTCTCTCTGGCCA[C/T]GTTAGACTCGGGAAG	9921
rs753757052	snp	C/G	1.67332e-05	0.00289246	intron-variant	RNF10	GRCh38.p7	12:120560909	GATGCATTGGAGATG[C/G]TAAACCTTTTCACTT	9921
rs753783245	snp	C/T	1.64917e-05	0.00287151	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120552509	TCTAGGTAGCAGAGG[C/T]TCAACGGGCAGAGTT	9921
rs753828007	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120566683	GGGAGGATCGCTTGA[G/T]CCTGGGAGGCAGAGG	9921
rs753914087	snp	A/G	1.65149e-05	0.00287353	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120566979	TCCAGGTTCCCATGC[A/G]GGTAAACAGGTGAAA	9921
rs753961310	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120539828	GGCTGTGCATCAGAA[A/T]CTCCTCAGGAACTTT	9921
rs753972908	snp	G/T	1.64738e-05	0.00286995	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120552607	CCCCGTGGCCAGACG[G/T]GTCACTTTGAAGGCA	9921
rs753976084	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120537875	GCAGGATATGTGGAG[A/G]TTAAAAGGTTAGGAA	9921
rs754004910	snp	G/T			utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576948	TTGACCCATGTGTAA[G/T]TAATTTTTCTCAACC	9921
rs754021603	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120574756	CATGGAGAAACCCCG[C/T]CTTTACTAAAAATAC	9921
rs754051396	snp	A/T	3.29544e-05	0.00405908	synonymous-codon, missense, nc-transcript-variant, intron-variant	RNF10	GRCh38.p7	12:120571207	CTTTCTGCTGACCCC[A/T]CTGTCACCCACTGCC	9921
rs754054379	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120564400	CAGCACTTTTGGGAG[A/G]CCTACTCAGGCAGAT	9921
rs754231274	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120560354	AGACGGGGTTTCACC[A/G]TGTTGGTCAGGCTGG	9921
rs754272036	snp	C/T	1.6486e-05	0.00287102	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576692	CCAGGCTACCTTCTC[C/T]ATCTGGTTTTTGTTT	9921
rs754280886	snp	A/T	1.66513e-05	0.00288537	intron-variant	RNF10	GRCh38.p7	12:120546396	TTCTTTTGTGTTTCT[A/T]GCTTTCAGATGGAAA	9921
rs754318302	snp	C/T	4.94189e-05	0.00497062	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120557591	TGTTGGTGATACCAT[C/T]ACGATGCAGCTGATG	9921
rs754318414	snp	C/T	1.64868e-05	0.00287109	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563810	GCCCCTTGTCCTCAG[C/T]GGAAGATGGACAGCA	9921
rs754371284	snp	A/C	1.65463e-05	0.00287626	intron-variant	RNF10	GRCh38.p7	12:120557714	TTGGGGACAAATAAT[A/C]CTGGGTACATTCTTT	9921
rs754417003	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120547270	TTGAGAGAGACCTAA[A/G]AGAAGCAAGGGAGCA	9921
rs754426221	snp	A/C	1.70377e-05	0.00291865	intron-variant	RNF10	GRCh38.p7	12:120565381	TGGGAGGAGGTAATG[A/C]CCATGTTGTCCTGGG	9921
rs754487704	in-del	-/A			intron-variant	RNF10	GRCh38.p7	12:120540085	GAGGAACTTAAAAAA[-/A]AAAAAAATAGGGGTG	9921
rs754506539	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120541244	ATCTTGAAAGCAGCA[A/G]TTAGGGTCAAACAGG	9921
rs754519126	snp	C/T	1.66521e-05	0.00288544	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120565478	AAGGCTCGGGAGGAA[C/T]GCCGCCGAGAGCGCA	9921
rs754558919	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120559625	CTTGATCTTGTGATC[C/T]GCCTACCTCAGCCTC	9921
rs754567659	snp	C/T	1.64732e-05	0.0028699	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120562969	GAGGCTCTGTCGGGA[C/T]TGGCCGGAAGCAGAA	9921
rs754650270	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120546002	AATCTGGTTATGTTA[C/T]AGTAATTTAAAAAGG	9921
rs754775331	snp	G/T	4.94254e-05	0.00497094	intron-variant	RNF10	GRCh38.p7	12:120575625	ACTTCTTTCCCACTT[G/T]GGCAGATGCTGAGGG	9921
rs754788650	snp	C/G	1.8365e-05	0.00303021	intron-variant	RNF10	GRCh38.p7	12:120552742	GGAAAGTAGGACTCT[C/G]CGGATAGCTGTGGTG	9921
rs754832287	in-del	-/TCTCCTGCCTTAGCCTCCTAAG	1.6476e-05	0.00287014	frameshift-variant, nc-transcript-variant	RNF10	GRCh38.p7	12:120554779	CTGATCCTGATACAT[-/TCTCCTGCCTTAGCCTCCTAAG]TAGTTAACTGGGACT	9921
rs754843780	snp	A/C/T	4.94241e-05	0.00497092	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120554758	CAAGACTACACAGCT[A/C/T]ATTTTGCTGATCCTG	9921
rs754895834	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120536280	AAAAAAAAAATTAGC[C/T]GAGTGTGGTGGCACA	9921
rs754896684	snp	A/T	5.64318e-05	0.00531157	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534819	CCCCGTTGATGCCGC[A/T]GAGCTCCCCCAACGC	9921
rs754921142	in-del	-/GAACAGCGGCTC	1.99289e-05	0.00315659	cds-indel, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534861	CTCCGACATGGACAA[-/GAACAGCGGCTC]GAACAGCGGCTCCAA	9921
rs754928488	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120565980	CTTTCGTAGCAGTAA[A/G]CACAGCCTTTTGATC	9921
rs754968382	snp	C/G	1.6473e-05	0.00286988	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563857	GTGAATGTGCGCTGC[C/G]TCGTGCGGGAGTACG	9921
rs754983515	snp	A/G			synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120552660	GAGGAACAAGTGGGG[A/G]CATAAGCCTTTTAAC	9921
rs755021451	snp	A/G	1.64844e-05	0.00287087	intron-variant	RNF10	GRCh38.p7	12:120563963	GGCCTTCCTGTAGAA[A/G]TGGAGGGTCAGGCAG	9921
rs755055689	snp	A/G	3.32779e-05	0.00407895	intron-variant	RNF10	GRCh38.p7	12:120560689	CATCGTGAGCTTTGA[A/G]TGTTGCATTTCTTTG	9921
rs755074952	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120562167	CTCCACCCTCTGATA[A/G]GCCTCAGTGTGTGTT	9921
rs755087608	snp	A/G	1.65231e-05	0.00287424	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546561	GCGGCGGCAGCAGCA[A/G]ACTCTTTAGCTCTTC	9921
rs755185411	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120543604	CTCAGGAGTTTGAGA[C/T]CCATCTGGGCAACAT	9921
rs755199385	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120574640	TTAAAACTGGAGGGT[A/G]CTTGGCTGGGCACGG	9921
rs755362992	in-del	-/TG			intron-variant	RNF10	GRCh38.p7	12:120546179	TGGTTTGATCTACGC[-/TG]TGTTTGTTTTGAGGG	9921
rs755367036	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120556927	GGAGGCCGAGGCGGG[C/T]GGATCACAAGGTCAG	9921
rs755403231	snp	C/G	1.64906e-05	0.00287142	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563410	TGTTCTCTGGACACT[C/G]CTTCTAGACCTCTTG	9921
rs755483090	snp	C/T	1.64743e-05	0.00287	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563063	AGTCTGTTTTTCAAC[C/T]CAGGAAGGTTAGTGT	9921
rs755555878	snp	C/T	1.64741e-05	0.00286998	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563052	CTTGGCGAAGGAGTC[C/T]GTTTTTCAACCCAGG	9921
rs755565273	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120537722	TAGAAAGCTTGACCA[C/T]GTTTGCCACCGCCAG	9921
rs755589433	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120537393	GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAT	9921
rs755622425	in-del	-/T	1.64735e-05	0.00286993	frameshift-variant, nc-transcript-variant	RNF10	GRCh38.p7	12:120557393	GCATCCTGCACTATC[-/T]TTTCACTGAGTGAGA	9921
rs755679496	snp	G/T	1.7887e-05	0.00299052	intron-variant	RNF10	GRCh38.p7	12:120563296	ATTTGCCACATTGCT[G/T]TCGGAAAGCAGGAGA	9921
rs755696361	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120547592	AGCCACCACACCTGG[C/G]CATGTTACATGGTTT	9921
rs755701684	in-del	-/CA			intron-variant	RNF10	GRCh38.p7	12:120567700	AGCGAGACTTTGTCT[-/CA]AAAAAAAAAAAAAAA	9921
rs755704139	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120567160	ACTTGCTATACTGAC[A/T]GCTTTACCCTGCCAG	9921
rs755719256	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120566654	GTGGTCCCGGCTACT[C/T]GGGAGGCTGAGGTGG	9921
rs755749788	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120536389	ATATCACGATACTGC[A/G]TACCATCCAGCCTGG	9921
rs755812957	snp	C/T	8.2373e-05	0.00641714	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575743	TTCCATAAAAGGCTG[C/T]TTCTAGAAAAAGAGT	9921
rs755887226	snp	C/T	1.64727e-05	0.00286986	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563863	GTGCGCTGCCTCGTG[C/T]GGGAGTACGGCAGCC	9921
rs755905816	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120543745	TTGGAGGCTGCAGTA[A/G]GCCGAGATCATGCCA	9921
rs755973320	snp	C/G/T	8.99817e-05	0.00670703	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534828	TGCCGCTGAGCTCCC[C/G/T]CAACGCCGCCGCCAC	9921
rs756024724	snp	C/T	1.91097e-05	0.00309103	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534886	CTCCAACAGCTCCTC[C/T]GCCTCTTCGGGCAGC	9921
rs756032228	in-del	-/T	1.64819e-05	0.00287066	intron-variant	RNF10	GRCh38.p7	12:120563956	GAGGTGAGGCCTTCC[-/T]GTAGAAATGGAGGGT	9921
rs756044100	snp	A/G/T			intron-variant	RNF10	GRCh38.p7	12:120553692	ACAGGCGTGAGCCAC[A/G/T]GCACCCAACCAGGAA	9921
rs756118625	in-del	-/A			intron-variant	RNF10	GRCh38.p7	12:120556631	AACTTAAGTTTTATT[-/A]AAAAAAAAATGAAGT	9921
rs756153614	snp	C/T	1.66588e-05	0.00288602	intron-variant	RNF10	GRCh38.p7	12:120560900	AGGTGAGAGGATGCA[C/T]TGGAGATGCTAAACC	9921
rs756157707	snp	A/G	1.6577e-05	0.00287893	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546581	TTTAGCTCTTCTTTT[A/G]ATGGTGGAAGACGAG	9921
rs756211252	snp	C/T	1.65111e-05	0.0028732	intron-variant	RNF10	GRCh38.p7	12:120552496	CATTCTCATTCTCTC[C/T]AGGTAGCAGAGGCTC	9921
rs756251731	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120564190	GTAGTTTGGGGATAT[A/G]GATATTTCTTTTATT	9921
rs756292620	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120562355	TCTCGGCTCATCACA[A/G]CCTCTGCCTCCAAGG	9921
rs756292933	snp	C/G			synonymous-codon, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575946	TACTTCAGATCCCCT[C/G]TCTGGTAAGGGCAGA	9921
rs756339801	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120563178	GAAGAGGGGACAATG[A/C]GTATTTTCTGTATGC	9921
rs756365497	in-del	-/AC			utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577067	CTTCCTGGACTCAGT[-/AC]ACCTCTCAGTTTGTC	9921
rs756469367	snp	G/T	1.64923e-05	0.00287156	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120566968	CTCAGCAGAAGTCCA[G/T]GTTCCCATGCAGGTA	9921
rs756471038	snp	C/G	3.29592e-05	0.00405938	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563422	ACTCCTTCTAGACCT[C/G]TTGCTCTCCCTCTGG	9921
rs756496956	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120571958	ATACTCAGCATTCCT[A/G]CATTCAGATAAGTGA	9921
rs756518610	snp	C/T	1.64765e-05	0.00287019	missense, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575897	CCTTCAGCCAAGCTA[C/T]TGAAGCAGCCTTCAT	9921
rs756519075	snp	C/T	1.64735e-05	0.00286993	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557571	ACAGAGTCACATCAG[C/T]ATGTTGTTGGTGATA	9921
rs756524465	snp	A/G	3.30169e-05	0.00406293	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563519	AGTTAGCAGATGACA[A/G]TCTTAAAGAGGGGAC	9921
rs756533232	snp	C/T	1.64789e-05	0.0028704	intron-variant	RNF10	GRCh38.p7	12:120557506	TAGATCCCAATCTCT[C/T]CACTCCTTGCCCTGC	9921
rs756546896	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120543295	GAGCATAGGAATTCC[A/G]TAAAAGCTCATCTGT	9921
rs756586217	snp	A/G	7.5092e-05	0.00612702	intron-variant	RNF10	GRCh38.p7	12:120535017	ACTGCCCCTGCTGCT[A/G]GGGAGAGTCGTTGCT	9921
rs756641247	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120551833	TATTACTCCATTCTC[-/T]CATTGCTATTAAGAA	9921
rs756652281	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120570829	CTTTTTCTTGGAGCT[A/G]TTTCATCCTTGTAAA	9921
rs756674770	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120539797	ACAGTAGTTCTTGGC[A/G]GTTGTTCTCAGTGGT	9921
rs756701021	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120553958	CGCCCAGGCTGGAGT[A/G]TAGTGGCGTGATCTC	9921
rs756720221	snp	C/G	9.89071e-05	0.00703163	intron-variant	RNF10	GRCh38.p7	12:120554821	GTGGTGAGTAGCTCA[C/G]CCAAGCCCATAAGCT	9921
rs756737286	snp	A/G	8.38838e-05	0.00647571	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534831	CGCTGAGCTCCCCCA[A/G]CGCCGCCGCCACCGC	9921
rs756778898	snp	A/G	4.94271e-05	0.00497102	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557325	GCCCAATATGCCTCT[A/G]TCCACCTACTGCAGC	9921
rs756841668	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120537568	GGGAGGCGGAGGTTG[C/G]AGTAAGCCAAGATTG	9921
rs756857035	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120555049	GTGTAAGCTGGGAAG[G/T]AGTAACCCCTTACCC	9921
rs756862406	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120567270	TAGTTTTTGTTTGAG[A/G]TACTCCCCTGTATGC	9921
rs756863067	snp	C/G	1.89224e-05	0.00307585	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534910	GGGCAGCAGCAAAGG[C/G]CAACAGCCGCCCCGC	9921
rs756896237	in-del	-/GTT	4.16103e-05	0.00456108	intron-variant	RNF10	GRCh38.p7	12:120565574	GCACTGCTGTACGTC[-/GTT]GTATAGAACTCTGTG	9921
rs756915829	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120568823	TGCTGTGATGCATTC[A/G]TTAGCTCACTGCAGT	9921
rs756976680	snp	C/T	1.64768e-05	0.00287021	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120565101	TCACAGATATCTCTC[C/T]CACTTGCCACTCACC	9921
rs756997830	snp	A/G	0.000428809	0.0146363	intron-variant	RNF10	GRCh38.p7	12:120563991	CAGCAGTATTAACCT[A/G]ATCTCTTTGAGGTAG	9921
rs757132399	snp	A/G	1.64866e-05	0.00287106	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120552513	GGTAGCAGAGGCTCA[A/G]CGGGCAGAGTTTAGC	9921
rs757148393	snp	A/G			intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120576090	TCTAGTGTCATTTAA[A/G]TAATACTCCATTTGG	9921
rs757154787	in-del	-/G			utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577488	CTTATGCCTTGGTTT[-/G]AGCTGAATTTGATGT	9921
rs757257007	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120539861	TTTTTCCCTCAAGAC[A/C]GTCTTGCTCTGTCAC	9921
rs757259089	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120552379	CACTCCAGCCTGGAT[A/G]ACAGAGTAAGACTCC	9921
rs757287340	snp	C/G	1.64762e-05	0.00287016	missense, nc-transcript-variant, intron-variant	RNF10	GRCh38.p7	12:120571214	CTGACCCCTCTGTCA[C/G]CCACTGCCAGTCAGG	9921
rs757309663	snp	A/C/G	4.9576e-05	0.00497855	intron-variant	RNF10	GRCh38.p7	12:120566984	GTTCCCATGCAGGTA[A/C/G]ACAGGTGAAATTTAA	9921
rs757414439	snp	A/G	1.66283e-05	0.00288338	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563551	ATTTGCACTGAGTCC[A/G]GCCAGCAGGAACCCA	9921
rs757468556	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120564597	CGGCAGAGCAAGACC[A/G]TGTCTCAGAAAAAAA	9921
rs757527818	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120538539	CTACAGCTTCATTCC[A/C]GTAGTGTTAATAGGT	9921
rs757609041	snp	A/G	5.52105e-05	0.00525378	intron-variant	RNF10	GRCh38.p7	12:120563635	CAAGGTGAGGGTGCC[A/G]GAAGAGAGGGCTGGG	9921
rs757634356	snp	A/C	4.94352e-05	0.00497143	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546464	GAACTTTCCTACCCC[A/C]AAAATGAAAGTTTTA	9921
rs757745516	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120540631	TCTCTCACTTGACAT[A/G]TCTGTCTTCATACCC	9921
rs757848397	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120559750	GCCCAGGCTGGAGTG[C/T]AATGGTGCGATCTTG	9921
rs757898926	snp	C/T	1.64784e-05	0.00287035	intron-variant	RNF10	GRCh38.p7	12:120557473	TCTCAAGAGGTGAGA[C/T]TGAGACATTTACTCA	9921
rs757898961	snp	A/C	2.02743e-05	0.00318383	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534936	CCCGCTCCGCCTCGG[A/C]GGGGCCAGCCGGCGA	9921
rs757931101	snp	C/T	4.96528e-05	0.00498236	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575994	TTGTCAAACATACTA[C/T]ACATGTACTGCCATT	9921
rs757948977	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120570648	TCTGTGGGAAGTGTT[C/T]AGCTCTAGTCAGAAT	9921
rs757950187	snp	G/T	1.68886e-05	0.00290586	intron-variant	RNF10	GRCh38.p7	12:120534986	AAGGACGGGCCTGCG[G/T]CAGTGGGCGGGGGCG	9921
rs757974587	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120545075	AGATTAAAAGGAAAA[C/T]ACTGTTAATGAGTTA	9921
rs757991242	snp	C/T	1.64735e-05	0.00286993	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120565142	GCATCTGTGAACTGG[C/T]TTTGCAACCTCCTGT	9921
rs758149147	snp	C/T	1.6476e-05	0.00287014	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120552636	CAGTGGACATGGTAG[C/T]TGGGGAAAGAGGAAC	9921
rs758180471	in-del	-/GCCGCCGAGGCCCCCGTTGAT	1.74595e-05	0.00295456	utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534792	GCTCCGACTGCCGTC[-/GCCGCCGAGGCCCCCGTTGAT]GCCGCCGAGGCCCCC	9921
rs758191279	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120569533	ACATTATTTGTGATA[C/T]GCATCTTTTTTTTTT	9921
rs758273973	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120564691	CTTCCTTCCCAGTTA[C/T]TTATTCTGTCAGTGG	9921
rs758286955	snp	A/G	1.76508e-05	0.00297071	intron-variant	RNF10	GRCh38.p7	12:120552728	CCCTCAGAGGAAAGG[A/G]AAAGTAGGACTCTCC	9921
rs758300709	snp	A/G			upstream-variant-2KB	RNF10	GRCh38.p7	12:120534093	CATTATTATCAGTGT[A/G]TATTATTATTGTTAC	9921
rs758309740	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120545864	TTTTAGAGCTCAACT[A/T]CTTTTGTTCTGTCAA	9921
rs758326654	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120565939	TTTGATAGACTAGGA[A/G]ATGCAGGAAGTTGGA	9921
rs758347475	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120542238	CCATCATAGCACACC[A/G]CAGCCTCAACCTTGG	9921
rs758361509	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577088	CTCAGTTTGTCTTTT[A/G]AAAAACAGCTGAATC	9921
rs758398303	snp	A/G	1.6476e-05	0.00287014	missense, synonymous-codon, nc-transcript-variant, intron-variant	RNF10	GRCh38.p7	12:120571227	CACCCACTGCCAGTC[A/G]GGGCAGTCCCTCATT	9921
rs758443878	snp	C/G	1.64746e-05	0.00287002	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563839	CATATGTTCCTGCAC[C/G]CTGTGAATGTGCGCT	9921
rs758451315	snp	A/C	1.6489e-05	0.00287128	intron-variant	RNF10	GRCh38.p7	12:120575601	CCAGCTACTTAAATT[A/C]TCTCCCCCACTTCTT	9921
rs758464691	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120573365	TCCCCTTTTTTTTCC[C/T]TTCCATGGCCAGTTG	9921
rs758533723	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120575112	ATTAGCCAGGCGGGT[A/G]CCTGTAATCCCAGCT	9921
rs758540605	snp	A/G	1.64735e-05	0.00286993	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557608	CGATGCAGCTGATGA[A/G]GAGGGAGAAAGGGGT	9921
rs758585796	snp	A/T			utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576752	GGCTGCTGTAATTTT[A/T]AAGTATTTGAGTTTG	9921
rs758586614	snp	C/G/T	3.29931e-05	0.00406149	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576715	TTTTGTTTTTGTTTT[C/G/T]TTTTCCCCCATGCTT	9921
rs758590273	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120551399	TCTCGGGTTCAAGCG[A/G]TTCTCCTGCCTCAGC	9921
rs758646358	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120540745	GAAATGAGCAGTTTA[C/G]TGTCTTATCAGTGAG	9921
rs758709939	snp	C/T	1.67178e-05	0.00289113	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120565492	ACGCCGCCGAGAGCG[C/T]AGGATTGAGATAGAG	9921
rs758828389	snp	A/G	1.6477e-05	0.00287024	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546471	CCTACCCCAAAAATG[A/G]AAGTTTTAACAACCA	9921
rs758895236	snp	C/T			missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563012	GTGTTGTGGCTGCTC[C/T]GGAACAACTGGTGCT	9921
rs758899278	snp	C/T			intron-variant, synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120574493	GGCCTGTGGTTGGAT[C/T]TGAAAGTTAATGATG	9921
rs758940510	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120560545	TTTCTTAGATTTCTT[A/G]TATCAAGAGCAGAGC	9921
rs758965467	snp	A/G	1.78163e-05	0.0029846	intron-variant	RNF10	GRCh38.p7	12:120563307	TGCTTTCGGAAAGCA[A/G]GAGATATCCTTTCTG	9921
rs758989247	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120561581	GAGTGATCAGCATTT[A/G]ATAGGACTTGTGCTA	9921
rs758993609	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120547728	AGGAGAGGTAGGAAA[C/T]GTACCCAAAGACTAG	9921
rs759013546	snp	A/C	0.000115637	0.00760295	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120560729	GCATTCTTATAGATG[A/C]ACAGCACAGCCAGTA	9921
rs759080117	snp	G/T	1.65386e-05	0.00287559	intron-variant	RNF10	GRCh38.p7	12:120557710	AATTTTGGGGACAAA[G/T]AATCCTGGGTACATT	9921
rs759149384	in-del	-/TGTGT			intron-variant	RNF10	GRCh38.p7	12:120567862	GCATTTCATTATGGG[-/TGTGT]GTGTGTGTGTGTGTG	9921
rs759168076	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120573797	CAGTTTCAAAATAGC[C/T]TTCAGCCAAGCTATT	9921
rs759218471	snp	A/G	1.64803e-05	0.00287052	intron-variant	RNF10	GRCh38.p7	12:120563116	CGTTCCTCAAATGCT[A/G]TCATTGAGCTGGTAG	9921
rs759252604	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120560254	CCTCCTGGGTTCAAG[C/G]GATTCTCCTGCCTCA	9921
rs759300613	in-del	-/A	1.64855e-05	0.00287097	frameshift-variant, nc-transcript-variant	RNF10	GRCh38.p7	12:120563416	CTGGACACTCCTTCT[-/A]GACCTCTTGCTCTCC	9921
rs759344486	snp	C/T	1.64817e-05	0.00287064	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120566836	GCAGACCCAGAAGTC[C/T]ACATTCCCCTCGAGA	9921
rs759376769	in-del	-/TCTGTT			upstream-variant-2KB	RNF10	GRCh38.p7	12:120532964	ATCTGCTTTTTGTTC[-/TCTGTT]TCTGTTTCTACTTTT	9921
rs759397407	snp	A/G	1.68613e-05	0.00290351	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563360	AGGGTGTGCTGGAGT[A/G]TCTGTCTGCCTTCGA	9921
rs759508911	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120537177	CGGGCGTGGTGGCAC[A/G]CACCTGTAGTCCCAG	9921
rs759510477	snp	C/T	1.64732e-05	0.0028699	synonymous-codon, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575829	TGCCCCTGTGGACAG[C/T]GACGGGGAGAGTGAT	9921
rs759554848	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120549166	CAAAAGGAAGGCCTG[A/G]TGATGGAGGTGGGTT	9921
rs759611212	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120562172	CCCTCTGATAGGCCT[C/T]AGTGTGTGTTCCCCT	9921
rs759631767	snp	A/C			synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120565484	CGGGAGGAACGCCGC[A/C]GAGAGCGCAGGATTG	9921
rs759679089	snp	A/G	1.64746e-05	0.00287002	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557408	CTTTCACTGAGTGAG[A/G]AGACGTGGAGTAAAT	9921
rs759679169	snp	A/C	1.93913e-05	0.00311372	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534877	GAACAGCGGCTCCAA[A/C]AGCTCCTCCGCCTCT	9921
rs759696966	snp	C/T	1.64887e-05	0.00287125	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120565187	CCCTAGAGATGTTCT[C/T]AGGTGAGAATGCCCC	9921
rs759735188	snp	C/T	2.10506e-05	0.00324421	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534959	GCCGGCGAGTCTAAA[C/T]CCAAGAGCGGTAAGG	9921
rs759807099	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120554545	TGCTGAGTCTTTGGG[G/T]TCTTTCCAGAGCTGG	9921
rs759865796	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120555891	CCTCTTGGGTTCAAG[C/G]AATTCTCATGCCTCA	9921
rs759868302	snp	C/T	3.29473e-05	0.00405864	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120552595	TTCACTTTTGAACCC[C/T]GTGGCCAGACGGGTC	9921
rs759875200	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120565559	TTTCATCTTTGACTA[A/G]CACTGCTGTACGTCG	9921
rs759889142	snp	C/T	1.64732e-05	0.0028699	intron-variant	RNF10	GRCh38.p7	12:120562924	CTTAACCTTCTCTGG[C/T]GTTCTCTCTGGCCAC	9921
rs759956116	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120545481	ACAGGCATGAGCCAC[C/T]GCGCCTGGCCATTTT	9921
rs759986975	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120564110	GTAAGTGAAGTGTCC[C/T]CTCAGCATGCCAGGG	9921
rs760001652	snp	C/G	5.06744e-05	0.00503335	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120576592	TGTCTCCCTTTAGAA[C/G]AGAAAGGAGGAAAGA	9921
rs760032886	snp	G/T	1.65192e-05	0.00287391	intron-variant	RNF10	GRCh38.p7	12:120571168	ACGTGACGAATATAA[G/T]CAGGTCTCTGGTTCC	9921
rs760043933	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120549356	AGGCACATGAGGGTC[C/T]ACTGTGGTGAGGCTG	9921
rs760065956	in-del	-/TT	1.64761e-05	0.00287015	frameshift-variant, nc-transcript-variant	RNF10	GRCh38.p7	12:120546520	ACAGAAAAGCAAGAC[-/TT]TTAACAAGATGCCTC	9921
rs760206216	snp	A/G	1.64781e-05	0.00287033	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120566848	GTCCACATTCCCCTC[A/G]AGAATCTACAGCAGT	9921
rs760265294	snp	A/G	1.64827e-05	0.00287073	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120566923	GGTCCCACCAGCACC[A/G]AGGGCCATGGGGCCC	9921
rs760298941	snp	G/T	1.67091e-05	0.00289038	intron-variant	RNF10	GRCh38.p7	12:120552451	GGTTTCTGCTATAAA[G/T]CAGTGTCATCCTAAT	9921
rs760319909	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120571371	GGGAACCTCCTCCAG[A/G]GATTGTTACCTCTCA	9921
rs760356960	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120576490	CTAATTCCAGAGCCT[C/T]CACTCTTAGCTCCCA	9921
rs760380903	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120575274	CTCACTGCTTCCTCC[A/G]ACAGCTCGATGTTTT	9921
rs760387340	snp	C/T	6.63856e-05	0.00576094	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557282	GGCATTTTGTTTCAG[C/T]GCATTTGTAGCCATG	9921
rs760433898	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120562691	TCACCACACTGTCTT[C/T]CACAATGATTGAACT	9921
rs760523271	snp	C/G	3.29457e-05	0.00405854	missense, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575833	CCTGTGGACAGCGAC[C/G]GGGAGAGTGATAATT	9921
rs760587634	snp	C/T	1.64961e-05	0.00287189	missense, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575947	ACTTCAGATCCCCTC[C/T]CTGGTAAGGGCAGAG	9921
rs760597028	in-del	-/AAACAG	1.65089e-05	0.00287301	cds-indel, nc-transcript-variant	RNF10	GRCh38.p7	12:120576616	GGAAAGAAAAGAAAA[-/AAACAG]AAACAGAAGCTCCTG	9921
rs760636693	snp	C/G	3.30289e-05	0.00406366	intron-variant	RNF10	GRCh38.p7	12:120565207	GAGAATGCCCCTGCT[C/G]TGCTTCTCTTTATAG	9921
rs760646652	snp	C/G	2.24474e-05	0.00335011	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534968	TCTAAACCCAAGAGC[C/G]GTAAGGACGGGCCTG	9921
rs760697990	snp	A/C	1.70464e-05	0.0029194	intron-variant	RNF10	GRCh38.p7	12:120546359	GCAGTTGGCTAAGTG[A/C]ATGTATCAGCTTCTT	9921
rs760709914	snp	A/G			intron-variant, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120539425	CTGTAGTAAGGCCAT[A/G]TGTTGCCCCTCTGGA	9921
rs760763949	snp	C/G	3.29451e-05	0.00405851	intron-variant	RNF10	GRCh38.p7	12:120562937	GGTGTTCTCTCTGGC[C/G]ACGTTAGACTCGGGA	9921
rs760793140	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120557824	GATTCCAGTAGGTTA[A/G]GGTGGGGTTTGTAGA	9921
rs760796158	in-del	-/T	1.73288e-05	0.00294348	intron-variant	RNF10	GRCh38.p7	12:120546638	TTCTAGAGCATAAGC[-/T]ATGAGATCTGATCCC	9921
rs760817063	snp	C/G	0.00069511	0.0186299	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563009	CTGGTGTTGTGGCTG[C/G]TCTGGAACAACTGGT	9921
rs760823520	snp	C/G	1.64738e-05	0.00286995	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120552601	TTTGAACCCCGTGGC[C/G]AGACGGGTCACTTTG	9921
rs760823912	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576877	ACCAAAATAAAGTAT[C/T]GACACAAGAGATCTC	9921
rs760832928	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120558671	CCTCCCGGGTTTGAG[C/T]GATTCTCGTGCCTCA	9921
rs760877996	snp	A/G			downstream-variant-500B	RNF10	GRCh38.p7	12:120577863	GTGTATGGTACTTTC[A/G]GTCTCATCCATTGTA	9921
rs760888395	snp	A/G			upstream-variant-2KB	RNF10	GRCh38.p7	12:120533992	AGCCTGGGCGACAGA[A/G]CGACTCCGCCTCAAA	9921
rs760961446	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120544683	GTGCATAAGTAATTA[C/T]TATGTTGTTAGAGTA	9921
rs760970566	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120553206	TTTTTGCCTCAGCCT[C/G]CCGAATAGCTGGGAC	9921
rs761015017	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120545607	CTGTGGCACGATCTC[A/G]GCTCACTGCAACCTC	9921
rs761017754	snp	A/G	1.71971e-05	0.00293227	intron-variant	RNF10	GRCh38.p7	12:120552711	CAAGTGAGTATTGCT[A/G]CCCCTCAGAGGAAAG	9921
rs761094767	snp	C/G	1.6507e-05	0.00287284	intron-variant, missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120571174	CGAATATAATCAGGT[C/G]TCTGGTTCCCTTTCA	9921
rs761116735	in-del	-/C	1.64732e-05	0.0028699	intron-variant	RNF10	GRCh38.p7	12:120562935	TGGTGTTCTCTCTGG[-/C]CCACGTTAGACTCGG	9921
rs761152008	snp	A/T	1.65302e-05	0.00287486	intron-variant	RNF10	GRCh38.p7	12:120571326	AGCAGCCCAGGGGTA[A/T]TTAACATGAACTCTG	9921
rs761193675	snp	C/T	0.000247954	0.0111317	utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534777	CCGCCGCGCCCGCTC[C/T]GCTCCGACTGCCGTC	9921
rs761199512	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120566375	AGACATTATAGAAGG[A/G]CAGTTATTGTAAATT	9921
rs761202876	snp	A/C	1.65042e-05	0.0028726	intron-variant	RNF10	GRCh38.p7	12:120563798	GTGTGTGATAGAGCC[A/C]CTTGTCCTCAGCGGA	9921
rs761264111	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120535428	ATTTAATAACCTGGT[C/G]CCAGATCCATTCCTC	9921
rs761276029	in-del	-/A			intron-variant	RNF10	GRCh38.p7	12:120559156	TCTTGCTATGTTGAT[-/A]AGGCTGGTCTTGAAC	9921
rs761338411	snp	C/T	1.64871e-05	0.00287111	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563489	AGGGGTTGCCAGAGG[C/T]CTGTGATGACTTGGA	9921
rs761350208	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120539522	CAGAAACTTGCTGAC[C/T]GGTATTCTGACCTCT	9921
rs761359348	snp	C/T	1.64836e-05	0.0028708	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120566950	GCCCTCTCCATTTCT[C/T]CTCTCAGCAGAAGTC	9921
rs761379310	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120570086	GAGATGGGGTTTCAC[C/T]GTGTTAGCCAGGATG	9921
rs761385594	snp	A/G	1.64754e-05	0.00287009	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557450	TACAGTTCTGTGCAT[A/G]AGAAGGATCTCAAGA	9921
rs761389436	snp	G/T	1.7271e-05	0.00293857	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563591	CAGGCTTCACACGCC[G/T]CAGCAGCTCTCCTTG	9921
rs761496796	snp	G/T	2.36376e-05	0.00343777	intron-variant	RNF10	GRCh38.p7	12:120534977	AAGAGCGGTAAGGAC[G/T]GGCCTGCGGCAGTGG	9921
rs761508466	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120564004	CTAATCTCTTTGAGG[A/T]AGGCCTAGCCATCCT	9921
rs761512968	snp	G/T			upstream-variant-2KB	RNF10	GRCh38.p7	12:120534207	GGGGCGGAGGTGGGG[G/T]AGGAAATAAAAAAAA	9921
rs761583876	snp	C/T	1.64751e-05	0.00287007	intron-variant	RNF10	GRCh38.p7	12:120557536	CTACATATGAGTGTC[C/T]ATGTTTCAGTGTTGT	9921
rs761708696	snp	C/T	1.70382e-05	0.0029187	intron-variant	RNF10	GRCh38.p7	12:120546366	GCTAAGTGAATGTAT[C/T]AGCTTCTTAAGACGT	9921
rs761732327	snp	A/G	1.64779e-05	0.00287031	stop-lost, nc-transcript-variant	RNF10	GRCh38.p7	12:120576666	CGTCCACACCAAGTG[A/G]CACTACTGGCCCAGG	9921
rs761797310	snp	A/C	1.64743e-05	0.00287	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563017	GTGGCTGCTCTGGAA[A/C]AACTGGTGCTGATGG	9921
rs761865712	in-del	-/TTTCCCACTTT	3.29636e-05	0.00405964	intron-variant	RNF10	GRCh38.p7	12:120575615	TCTCTCCCCCACTTC[-/TTTCCCACTTT]GGCAGATGCTGAGGG	9921
rs761905166	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120536791	AACTGTGAATTCTCA[A/G]CTAATTTTTCTGGGG	9921
rs761909944	snp	C/T			downstream-variant-500B	RNF10	GRCh38.p7	12:120578083	ACCATGCAGTAATGA[C/T]GTCAGATGAGGCCAG	9921
rs761962636	in-del	-/AG	1.73818e-05	0.00294798	intron-variant	RNF10	GRCh38.p7	12:120552718	GTATTGCTACCCCTC[-/AG]AGGAAAGGGAAAGTA	9921
rs762003332	snp	C/T	8.23744e-05	0.0064172	intron-variant	RNF10	GRCh38.p7	12:120563089	AGTGTGTTCCTGTTA[C/T]TAAGTGGCTGCCGTT	9921
rs762006401	in-del	-/TTGTT			intron-variant	RNF10	GRCh38.p7	12:120572590	TGCCAAATACTTGTT[-/TTGTT]TTGTTTTGTTTTGTT	9921
rs762027692	in-del	-/GAA	0.000232728	0.0107847	cds-indel, nc-transcript-variant	RNF10	GRCh38.p7	12:120563377	CTGTCTGCCTTCGAT[-/GAA]GAAACCACGGAAGTT	9921
rs762035397	snp	A/G	0.000107187	0.00731997	utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534790	TCCGCTCCGACTGCC[A/G]TCGCCGCCGAGGCCC	9921
rs762116863	snp	A/G			upstream-variant-2KB	RNF10	GRCh38.p7	12:120533734	ATAAATTGGCCGGGC[A/G]CGGTGGCTCACGTCT	9921
rs762151714	snp	C/G	0.000185995	0.00964172	intron-variant	RNF10	GRCh38.p7	12:120574437	ATTCCTCAGGGGCAT[C/G]AGGATTGTTCTGATT	9921
rs762157169	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120542861	GGCCTTAAATTGTAA[C/G]TAAGGTAAGGGTCAC	9921
rs762192274	in-del	-/A/AA			intron-variant	RNF10	GRCh38.p7	12:120557088	ATGGACCGTCTCAAA[-/A/AA]AAAAAAAAAAAAAGA	9921
rs762235020	snp	C/G	1.64833e-05	0.00287078	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563811	CCCCTTGTCCTCAGC[C/G]GAAGATGGACAGCAT	9921
rs762340321	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120554167	GCCTCGGCCTCCCAA[A/C]GTGCTGGGATTACAG	9921
rs762347532	snp	A/G	1.65021e-05	0.00287241	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120560737	ATAGATGAACAGCAC[A/G]GCCAGTACTCCAAGT	9921
rs762387931	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120548421	TCAGGGCGGGAGGAA[A/T]ATTGCTGAAAGGTGT	9921
rs762390030	snp	C/T	1.65392e-05	0.00287564	intron-variant	RNF10	GRCh38.p7	12:120563784	ACTGGCCAAGACTGG[C/T]GTGTGATAGAGCCCC	9921
rs762445284	snp	A/C	1.65143e-05	0.00287348	intron-variant	RNF10	GRCh38.p7	12:120557694	GGAGGTGAGTTCTTT[A/C]AATTTTGGGGACAAA	9921
rs762493166	snp	C/T	3.49834e-05	0.00418216	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563602	CGCCTCAGCAGCTCT[C/T]CTTGTTACTACTTTT	9921
rs762526605	snp	G/T	1.69815e-05	0.00291384	intron-variant	RNF10	GRCh38.p7	12:120546371	GTGAATGTATCAGCT[G/T]CTTAAGACGTTCTTT	9921
rs762680687	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120548186	TGTACATTGAAATTC[A/C]TATTTGATAAATATA	9921
rs762683304	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120571839	AGATTGTCTTGGTTA[C/T]ACTGCACCTAGCCAA	9921
rs762695838	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120540924	TAGTGGTGCAGTCTC[C/G]GCCTTGCCGCAACCT	9921
rs762733330	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120540391	GATTTAAAACTTCAC[C/G]CATAGTTCCTTCTCC	9921
rs762812058	snp	C/T	1.66355e-05	0.002884	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120565469	CGCCAAAAGAAGGCT[C/T]GGGAGGAACGCCGCC	9921
rs762864761	snp	A/G	1.82174e-05	0.00301801	intron-variant	RNF10	GRCh38.p7	12:120565542	AGTGTAAGTTCAGGA[A/G]CTTTCATCTTTGACT	9921
rs762864903	snp	C/T	3.29462e-05	0.00405857	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563027	TGGAACAACTGGTGC[C/T]GATGGCTCCCTTGGC	9921
rs762887275	snp	C/T			upstream-variant-2KB	RNF10	GRCh38.p7	12:120533515	CTTATGGCCTGTTTC[C/T]GCCTCTGTCTCCTGG	9921
rs762917964	snp	C/T	0.000148301	0.00860978	intron-variant	RNF10	GRCh38.p7	12:120563108	GTGGCTGCCGTTCCT[C/T]AAATGCTGTCATTGA	9921
rs762981364	snp	A/G	1.68633e-05	0.00290368	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534814	GAGGCCCCCGTTGAT[A/G]CCGCTGAGCTCCCCC	9921
rs763081348	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120537037	TTGACCAAAGCAAGT[A/G]TTTGTCATTGTTAAC	9921
rs763106217	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120553545	GAGTAGCTGGGACTA[C/T]AGGCGCCCACCCCCT	9921
rs763107187	snp	C/T	6.58924e-05	0.0057395	missense, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575819	TAGTTCCTCCTGCCC[C/T]TGTGGACAGCGACGG	9921
rs763143106	snp	G/T	1.69879e-05	0.00291439	intron-variant	RNF10	GRCh38.p7	12:120557231	CTAAAACTTTGACAG[G/T]CCCTAATCAGTTCTT	9921
rs763178057	snp	C/T	3.29549e-05	0.00405911	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563928	GGTGGAGATTGCTGG[C/T]TACTCCATGTCTGAG	9921
rs763196486	snp	C/T	0.00011805	0.00768186	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534868	CATGGACAAGAACAG[C/T]GGCTCCAACAGCTCC	9921
rs763196976	in-del	-/G	1.64789e-05	0.0028704	frameshift-variant, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575913	TGAAGCAGCCTTCAT[-/G]AAACTGGACACACCA	9921
rs763224205	snp	C/T	3.30398e-05	0.00406434	intron-variant	RNF10	GRCh38.p7	12:120565067	TGGTCCTTTTTCCAA[C/T]GTAGGATGTTCGACA	9921
rs763277140	snp	C/G/T	6.59689e-05	0.00574288	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120560847	GGAGAAGCACACTCC[C/G/T]GAGTCCTGCTTTATT	9921
rs763373754	snp	C/T	1.6483e-05	0.00287076	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120560784	GGAGCAGGTGCTGCA[C/T]CGGGTAGTTCTGGAG	9921
rs763384533	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120575479	ATATAGAGGACATGA[C/G]TAGAACAGTGTGTTA	9921
rs763431421	snp	C/T	1.64757e-05	0.00287012	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120566881	CCTGCCTTCAATTCT[C/T]ATACCTGCTCCTCTG	9921
rs763439286	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120576499	GAGCCTCCACTCTTA[C/G]CTCCCACTCTGTGAC	9921
rs763444530	in-del	-/A			intron-variant	RNF10	GRCh38.p7	12:120566764	GAGACCCCATCTCAA[-/A]AAAAAAAAAAAAAAA	9921
rs763514111	snp	A/C	3.32591e-05	0.0040778	intron-variant	RNF10	GRCh38.p7	12:120552472	TCATCCTAATCTGAA[A/C]TACTGATTCATTCTC	9921
rs763525880	snp	G/T	1.64773e-05	0.00287026	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120566855	TTCCCCTCGAGAATC[G/T]ACAGCAGTTTCCTGC	9921
rs763567441	snp	G/T	3.29462e-05	0.00405857	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120552571	ATCAACCTGAACCAC[G/T]TGTTGAATTTCACTT	9921
rs763602182	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120548470	TTGTCAAGTGTTGCT[A/G]ATAGGTTAAGAATAG	9921
rs763690328	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120568646	ATGCCTGGCTAATTT[C/T]TGTATTTTTAATAGA	9921
rs763695637	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120549405	GTTAGCCCTGTTTGT[C/T]TGCTGCAGGGCTGAT	9921
rs763713065	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120538540	TACAGCTTCATTCCA[A/G]TAGTGTTAATAGGTA	9921
rs763743417	snp	C/T	9.88533e-05	0.00702971	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120557431	GAGTAAATGTCCCAT[C/T]TGTTACAGTTCTGTG	9921
rs763780862	snp	A/C/G	4.94558e-05	0.00497251	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563488	GAGGGGTTGCCAGAG[A/C/G]CCTGTGATGACTTGG	9921
rs763792133	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120556248	GACCTTAAAGCTTGA[A/G]CTCTCGCCGGGCGCG	9921
rs763798530	snp	A/G	2.25446e-05	0.00335735	intron-variant	RNF10	GRCh38.p7	12:120534971	AAACCCAAGAGCGGT[A/G]AGGACGGGCCTGCGG	9921
rs763843029	snp	C/G	1.65704e-05	0.00287836	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120557284	CATTTTGTTTCAGCG[C/G]ATTTGTAGCCATGAA	9921
rs763897888	snp	C/G	1.89669e-05	0.00307946	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534894	GCTCCTCCGCCTCTT[C/G]GGGCAGCAGCAAAGG	9921
rs763923022	snp	A/G	1.6473e-05	0.00286988	synonymous-codon, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575835	TGTGGACAGCGACGG[A/G]GAGAGTGATAATTCA	9921
rs763935722	in-del	-/GTTTTT	0.00136771	0.0261148	cds-indel, nc-transcript-variant	RNF10	GRCh38.p7	12:120576698	TACCTTCTCCATCTG[-/GTTTTT]GTTTTTGTTTTTTTT	9921
rs764067261	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120574285	ACAAGGCATCCCTGC[C/T]TGAACCCCATGGGGT	9921
rs764068894	snp	C/T			downstream-variant-500B	RNF10	GRCh38.p7	12:120577966	CCTACTTCCTGTGAG[C/T]ATGGCAGTCTGACTT	9921
rs764120071	in-del	-/GCAGAGGCTCAACGG	6.60022e-05	0.00574428	cds-indel, nc-transcript-variant	RNF10	GRCh38.p7	12:120552502	CATTCTCTCTAGGTA[-/GCAGAGGCTCAACGG]GCAGAGTTTAGCCCT	9921
rs764143150	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120564313	TACTATAAATTTTTC[A/G]TCAAACATATGCAGA	9921
rs764174595	in-del	-/TT			intron-variant	RNF10	GRCh38.p7	12:120547998	ATATAGAGCCAAGAC[-/TT]TTTGTTAGATGTGGG	9921
rs764191166	snp	A/G	6.58892e-05	0.00573936	intron-variant	RNF10	GRCh38.p7	12:120562938	GTGTTCTCTCTGGCC[A/G]CGTTAGACTCGGGAA	9921
rs764196710	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120565791	TCCAGAGATGGGAAT[C/T]GGGGCTTCGCTAAGA	9921
rs764231524	in-del	-/TTTTTTTTTTTTTTTTTTTTTTTTT			intron-variant	RNF10	GRCh38.p7	12:120553057	TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT	9921
rs764362163	snp	C/T	1.72412e-05	0.00293604	intron-variant	RNF10	GRCh38.p7	12:120552712	AAGTGAGTATTGCTA[C/T]CCCTCAGAGGAAAGG	9921
rs764421624	snp	C/T			upstream-variant-2KB	RNF10	GRCh38.p7	12:120533659	GTTATTATTATTATT[C/T]CTAATATGAGATAGA	9921
rs764456627	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120553571	CCCTGGCTAATTTTG[-/T]TTTTTGTATTTTTAG	9921
rs764483134	snp	A/C	1.83051e-05	0.00302527	intron-variant	RNF10	GRCh38.p7	12:120563633	ACCAAGGTGAGGGTG[A/C]CGGAAGAGAGGGCTG	9921
rs764485279	snp	A/C/G	3.31149e-05	0.00406898	intron-variant	RNF10	GRCh38.p7	12:120571334	AGGGGTATTTAACAT[A/C/G]AACTCTGCTGCTCAT	9921
rs764535790	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120552326	AGTCACTTGAACCTG[A/G]GAGGCAGAGGTTGCA	9921
rs764613670	snp	C/T	1.64822e-05	0.00287068	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576689	GGCCCAGGCTACCTT[C/T]TCCATCTGGTTTTTG	9921
rs764621612	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120540419	CCCAGGAACTTGATA[-/T]TTTTTTGTTTTCCAA	9921
rs764647074	snp	C/T	4.94189e-05	0.00497062	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557587	ATGTTGTTGGTGATA[C/T]CATTACGATGCAGCT	9921
rs764649043	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120566183	TGGGGTCCCAACACC[A/G]TGTAGGTGTTTGGCA	9921
rs764681226	snp	C/T	3.30028e-05	0.00406205	intron-variant	RNF10	GRCh38.p7	12:120563799	TGTGTGATAGAGCCC[C/T]TTGTCCTCAGCGGAA	9921
rs764739398	snp	A/G	4.94311e-05	0.00497123	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557463	ATAAGAAGGATCTCA[A/G]GAGGTGAGATTGAGA	9921
rs764760050	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120571671	GAGTTTAGAATATTT[A/T]AAAAATCATTTGATA	9921
rs764779913	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120573804	AAAATAGCCTTCAGC[C/G]AAGCTATTGAAGCAG	9921
rs764881493	in-del	-/T	0.00131154	0.0255744	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576711	TGGTTTTTGTTTTTG[-/T]TTTTTTTTCCCCCAT	9921
rs764916940	snp	A/G	1.70113e-05	0.00291639	intron-variant	RNF10	GRCh38.p7	12:120546368	TAAGTGAATGTATCA[A/G]CTTCTTAAGACGTTC	9921
rs764993020	snp	C/T			upstream-variant-2KB	RNF10	GRCh38.p7	12:120533809	TCAGGAGATCAAGAC[C/T]ATCCTGGCTAACACG	9921
rs765006055	snp	C/T	5.17558e-05	0.00508677	intron-variant	RNF10	GRCh38.p7	12:120534984	GTAAGGACGGGCCTG[C/T]GGCAGTGGGCGGGGG	9921
rs765006275	snp	A/C	1.65337e-05	0.00287517	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575985	TGCCCAGGGTTGTCA[A/C]ACATACTACACATGT	9921
rs765059446	snp	A/G	1.64779e-05	0.00287031	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576671	ACACCAAGTGACACT[A/G]CTGGCCCAGGCTACC	9921
rs765061391	snp	C/T	3.30677e-05	0.00406605	intron-variant	RNF10	GRCh38.p7	12:120565223	TGCTTCTCTTTATAG[C/T]AGGGTTCAGGGATTC	9921
rs765074961	snp	A/G	1.6473e-05	0.00286988	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120562950	GCCACGTTAGACTCG[A/G]GAAGAGGCTCTGTCG	9921
rs765218080	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120566519	ATAATCCCAACACTT[C/T]GGGAGGCCAAGGTGG	9921
rs765236118	snp	A/T	1.64773e-05	0.00287026	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120554727	TTCTAGCTGCCAATT[A/T]GTGGTGTCTGAAGAC	9921
rs765254101	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120537970	AGTGCTACTACAGCA[G/T]ATACTCAGGAGCTCT	9921
rs765263258	snp	A/G	1.64738e-05	0.00286995	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563019	GGCTGCTCTGGAACA[A/G]CTGGTGCTGATGGCT	9921
rs765302074	snp	G/T	1.64762e-05	0.00287016	missense, nc-transcript-variant, intron-variant	RNF10	GRCh38.p7	12:120571220	CCTCTGTCACCCACT[G/T]CCAGTCAGGGCAGTC	9921
rs765308571	snp	A/C	0.000191326	0.00977887	intron-variant	RNF10	GRCh38.p7	12:120552718	GTATTGCTACCCCTC[A/C]GAGGAAAGGGAAAGT	9921
rs765429535	snp	G/T	1.64784e-05	0.00287035	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563819	CCTCAGCGGAAGATG[G/T]ACAGCATATGTTCCT	9921
rs765438052	in-del	-/TTA			upstream-variant-2KB	RNF10	GRCh38.p7	12:120533645	TTGTCATTATTAACG[-/TTA]TTATTATTATTCCTA	9921
rs765438222	in-del	-/GGA	1.65051e-05	0.00287267	cds-indel, nc-transcript-variant	RNF10	GRCh38.p7	12:120563402	GGAAGTTTGTTCTCT[-/GGA]GGACACTCCTTCTAG	9921
rs765440875	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120565878	TTTATTAAAGGGACC[A/G]GCTATACACAGCAAG	9921
rs765461181	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120535797	CTACCTTTAATTGAG[A/G]GCTTACCATGTGCCA	9921
rs765501811	snp	A/C/G	0.00015436	0.0087841	utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534807	CGCCGCCGAGGCCCC[A/C/G]GTTGATGCCGCTGAG	9921
rs765600693	snp	C/T	1.64751e-05	0.00287007	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563921	CAACTGTGGTGGAGA[C/T]TGCTGGCTACTCCAT	9921
rs765682614	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120574402	AGTTACAAAGCTGGC[C/T]TTGGCCAAGTGGAAT	9921
rs765706820	snp	A/C/G	3.2955e-05	0.00405914	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546468	TTTCCTACCCCAAAA[A/C/G]TGAAAGTTTTAACAA	9921
rs765722815	in-del	-/TG			intron-variant	RNF10	GRCh38.p7	12:120559090	TTTTAAAAAATTAAC[-/TG]GGCATGCAGGTATAG	9921
rs765752791	snp	A/G	6.62504e-05	0.00575507	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575999	AAACATACTACACAT[A/G]TACTGCCATTCCCGC	9921
rs765765405	snp	C/T	3.29473e-05	0.00405864	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557565	GTTGCCACAGAGTCA[C/T]ATCAGTATGTTGTTG	9921
rs765903787	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120572807	GGTTTTACCATGTTG[A/G]CCAGGCTGGTCTAGA	9921
rs765908198	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120540426	AACTTGATATTTTTT[A/G]TTTTCCAAAATCTAA	9921
rs765908876	snp	C/G/T	4.94999e-05	0.00497473	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120546547	GCCTCCTCAAAGGGG[C/G/T]GGCGGCAGCAGCAAA	9921
rs765915281	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120545865	TTTAGAGCTCAACTT[C/G]TTTTGTTCTGTCAAT	9921
rs765926463	snp	A/G	1.65176e-05	0.00287376	intron-variant	RNF10	GRCh38.p7	12:120557695	GAGGTGAGTTCTTTA[A/G]ATTTTGGGGACAAAT	9921
rs766017568	in-del	-/TTT			intron-variant	RNF10	GRCh38.p7	12:120564292	TTTAAAATTAGACTC[-/TTT]GAGTACTATAAATTT	9921
rs766018940	snp	C/T	1.84106e-05	0.00303397	intron-variant	RNF10	GRCh38.p7	12:120565545	GTAAGTTCAGGAACT[C/T]TCATCTTTGACTAGC	9921
rs766053813	snp	C/G	1.64789e-05	0.0028704	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576676	AAGTGACACTACTGG[C/G]CCAGGCTACCTTCTC	9921
rs766103524	in-del	-/A	1.64912e-05	0.00287147	intron-variant	RNF10	GRCh38.p7	12:120554708	TTTTCCTGTCTTTCC[-/A]TATTTCTAGCTGCCA	9921
rs766105279	snp	A/G/T	3.32714e-05	0.00407858	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120565470	GCCAAAAGAAGGCTC[A/G/T]GGAGGAACGCCGCCG	9921
rs766158251	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120551335	AGTTTTGCTCTTGAT[A/G]CCAGGCTGGAGTGCA	9921
rs766220288	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120537043	AAAGCAAGTATTTGT[C/T]ATTGTTAACATTTCA	9921
rs766233079	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120536126	GTCAAGATTAAAAAA[A/G]CTGTTTAGAGTGAGA	9921
rs766257458	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120547130	ATTACGTTTCATACC[A/G]TGCAATTATGATAGA	9921
rs766289075	snp	A/G	1.77137e-05	0.00297599	intron-variant	RNF10	GRCh38.p7	12:120552731	TCAGAGGAAAGGGAA[A/G]GTAGGACTCTCCGGA	9921
rs766368122	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120554428	GCTTACTGCTGTTTG[A/T]TGGAGTCACGGTCTA	9921
rs766374320	snp	C/T	9.79288e-05	0.00699677	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534871	GGACAAGAACAGCGG[C/T]TCCAACAGCTCCTCC	9921
rs766382214	snp	C/G	4.94222e-05	0.00497078	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575722	TGAAGGGGGAGTTTG[C/G]CTTCTTTCCATAAAA	9921
rs766392801	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120574540	AGCAGACTAAAAGGT[A/C]GTGAGGGGCTGTTGA	9921
rs766405489	snp	C/T	1.64814e-05	0.00287061	intron-variant	RNF10	GRCh38.p7	12:120563114	GCCGTTCCTCAAATG[C/T]TGTCATTGAGCTGGT	9921
rs766434646	snp	G/T	6.06447e-05	0.00550624	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534817	GCCCCCGTTGATGCC[G/T]CTGAGCTCCCCCAAC	9921
rs766460552	snp	A/C	1.64749e-05	0.00287005	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120554745	GGTGTCTGAAGACCA[A/C]GACTACACAGCTCAT	9921
rs766477414	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120542328	TGGGCTAATTTTTAA[A/G]TTTTTTGTAGAGATG	9921
rs766629772	snp	A/G	1.65176e-05	0.00287376	intron-variant	RNF10	GRCh38.p7	12:120565068	GGTCCTTTTTCCAAT[A/G]TAGGATGTTCGACAG	9921
rs766649169	in-del	-/AGTG			intron-variant	RNF10	GRCh38.p7	12:120540755	GTTTACTGTCTTATC[-/AGTG]AGCATTTCTGTAAGC	9921
rs766691991	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120537596	TTGCACCATTGCACT[C/T]CAGCCCGTCTAAAAA	9921
rs766798936	snp	C/T	3.3012e-05	0.00406262	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120546550	TCCTCAAAGGGGCGG[C/T]GGCAGCAGCAAACTC	9921
rs766844119	snp	C/T	1.64833e-05	0.00287078	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120566952	CCTCTCCATTTCTCC[C/T]CTCAGCAGAAGTCCA	9921
rs766872494	in-del	-/A			intron-variant	RNF10	GRCh38.p7	12:120536263	CCTCGTCTCCATAAG[-/A]AAAAAAAAAAATTAG	9921
rs766878683	snp	C/T	5.00079e-05	0.00500015	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120565481	GCTCGGGAGGAACGC[C/T]GCCGAGAGCGCAGGA	9921
rs766893019	snp	C/T	1.64792e-05	0.00287042	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120546460	ACGTGAACTTTCCTA[C/T]CCCAAAAATGAAAGT	9921
rs766908827	snp	A/T	3.29511e-05	0.00405887	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120566882	CTGCCTTCAATTCTT[A/T]TACCTGCTCCTCTGA	9921
rs766948585	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120565912	GCCAGGTGGGTCTGA[-/T]AAGATGGAAATTTTG	9921
rs767015719	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120560345	CTTTAGTAGAGACGG[C/G]GTTTCACCATGTTGG	9921
rs767045849	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120561258	ATTCTATTCTAGAGG[C/T]GTTTTGAAAGACATT	9921
rs767218978	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120574323	TTGATATTTTTCCAG[C/G]AATAAAATGTTCTCT	9921
rs767247967	snp	C/T	3.57884e-05	0.00423	intron-variant	RNF10	GRCh38.p7	12:120563289	GGTCTGCATTTGCCA[C/T]ATTGCTTTCGGAAAG	9921
rs767255282	in-del	-/AAG	1.65538e-05	0.00287691	cds-indel, nc-transcript-variant	RNF10	GRCh38.p7	12:120576609	GAAAGGAGGAAAGAA[-/AAG]AAAAAAACAGAAACA	9921
rs767337093	in-del	-/GAG	1.6476e-05	0.00287014	cds-indel, nc-transcript-variant	RNF10	GRCh38.p7	12:120563443	CTCCCTCTGGTAGAA[-/GAG]GAGGAAGCAGTGTCT	9921
rs767433773	snp	C/G	5.14178e-05	0.00507014	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534823	GTTGATGCCGCTGAG[C/G]TCCCCCAACGCCGCC	9921
rs767437490	snp	A/G	1.68547e-05	0.00290294	intron-variant	RNF10	GRCh38.p7	12:120557255	AGTTCTTCAAGCAGT[A/G]AACCTTCTGGTGGCA	9921
rs767463807	snp	G/T	1.64844e-05	0.00287087	intron-variant	RNF10	GRCh38.p7	12:120563964	GCCTTCCTGTAGAAA[G/T]GGAGGGTCAGGCAGC	9921
rs767486283	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120550789	TTTTAGTAGAGACAG[A/G]GTTTCACTGTGTTAG	9921
rs767509811	snp	A/G	1.64732e-05	0.0028699	missense, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575830	GCCCCTGTGGACAGC[A/G]ACGGGGAGAGTGATA	9921
rs767518780	snp	A/G	0.000197817	0.00994332	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120565085	AGGATGTTCGACAGC[A/G]TCACAGATATCTCTC	9921
rs767576998	in-del	-/T	3.34493e-05	0.00408944	intron-variant	RNF10	GRCh38.p7	12:120546391	AGACGTTCTTTTGTG[-/T]TTCTTGCTTTCAGAT	9921
rs767633855	snp	A/G	1.93134e-05	0.00310746	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534879	ACAGCGGCTCCAACA[A/G]CTCCTCCGCCTCTTC	9921
rs767685238	snp	A/G	2.14788e-05	0.00327703	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534963	GCGAGTCTAAACCCA[A/G]GAGCGGTAAGGACGG	9921
rs767711233	snp	A/G	1.65337e-05	0.00287517	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120560880	GGCAGCTATCCAGGA[A/G]CTCAAGGTGAGAGGA	9921
rs767764480	snp	C/T	1.64762e-05	0.00287016	intron-variant	RNF10	GRCh38.p7	12:120562928	ACCTTCTCTGGTGTT[C/T]TCTCTGGCCACGTTA	9921
rs767775588	in-del	-/GAATT			intron-variant	RNF10	GRCh38.p7	12:120567967	TAAATGTATAGAAAA[-/GAATT]GAATTGAAGGCCAGG	9921
rs767818652	in-del	-/AAA			intron-variant	RNF10	GRCh38.p7	12:120558438	GCAACTTAAAACATT[-/AAA]AATGTGTATTAATTA	9921
rs767878008	snp	A/G	1.64735e-05	0.00286993	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120552596	TCACTTTTGAACCCC[A/G]TGGCCAGACGGGTCA	9921
rs767928782	snp	A/G	1.64852e-05	0.00287094	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120566957	CCATTTCTCCTCTCA[A/G]CAGAAGTCCAGGTTC	9921
rs767950860	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120564112	AAGTGAAGTGTCCCC[C/T]CAGCATGCCAGGGTT	9921
rs767956452	snp	C/T	1.75523e-05	0.00296241	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563605	CTCAGCAGCTCTCCT[C/T]GTTACTACTTTTACC	9921
rs767972334	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120539584	AAATGAAGATGCCAA[A/G]TAATTTAACTGTGAA	9921
rs768056108	snp	A/T	1.65021e-05	0.00287241	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563513	ACTTGGAGTTAGCAG[A/T]TGACAATCTTAAAGA	9921
rs768109281	snp	A/C	1.64792e-05	0.00287042	intron-variant	RNF10	GRCh38.p7	12:120557494	CATTTACTCAGTTAG[A/C]TCCCAATCTCTTCAC	9921
rs768131174	snp	A/G	1.65119e-05	0.00287327	intron-variant, splice-acceptor-variant	RNF10	GRCh38.p7	12:120571170	GTGACGAATATAATC[A/G]GGTCTCTGGTTCCCT	9921
rs768143625	in-del	-/GCA	6.60289e-05	0.00574544	cds-indel, nc-transcript-variant	RNF10	GRCh38.p7	12:120546551	CTCAAAGGGGCGGCG[-/GCA]GCAGCAGCAAACTCT	9921
rs768278078	snp	G/T	1.82108e-05	0.00301746	intron-variant	RNF10	GRCh38.p7	12:120563632	TACCAAGGTGAGGGT[G/T]CCGGAAGAGAGGGCT	9921
rs768295370	snp	A/C/G			intron-variant	RNF10	GRCh38.p7	12:120576439	CAAAGACACCCACTT[A/C/G]GTGTATACCAAGACT	9921
rs768331600	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120550408	GATAAAAGGTTGAGA[A/G]TGTGGAGGATTTTGT	9921
rs768394534	snp	C/T	3.41588e-05	0.00413258	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563583	CACCAAGTCAGGCTT[C/T]ACACGCCTCAGCAGC	9921
rs768442752	snp	A/T	0.000271334	0.0116444	intron-variant, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120539447	CCCTCTGGAGGTGCT[A/T]GTCAACTACTCTGGA	9921
rs768445341	snp	A/G	3.75361e-05	0.00433205	intron-variant	RNF10	GRCh38.p7	12:120563672	CAGAGGTGTTTCAGA[A/G]GTGACCCGGTGCTCT	9921
rs768499730	snp	C/G	1.64749e-05	0.00287005	intron-variant	RNF10	GRCh38.p7	12:120557531	CCCTGCTACATATGA[C/G]TGTCCATGTTTCAGT	9921
rs768503669	in-del	-/TCTG			intron-variant	RNF10	GRCh38.p7	12:120564066	TGTATTTTTAGTCTT[-/TCTG]TCAGTGATGGTGCTG	9921
rs768635121	snp	A/G	1.64741e-05	0.00286998	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563014	GTTGTGGCTGCTCTG[A/G]AACAACTGGTGCTGA	9921
rs768693625	snp	C/T	5.11217e-05	0.00505552	intron-variant	RNF10	GRCh38.p7	12:120546361	AGTTGGCTAAGTGAA[C/T]GTATCAGCTTCTTAA	9921
rs768730816	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120570434	CAGGTGATCCACCCA[C/T]CTCAGCCTCCCAAAG	9921
rs768732657	in-del	-/C	1.64735e-05	0.00286993	frameshift-variant, nc-transcript-variant	RNF10	GRCh38.p7	12:120563056	CGAAGGAGTCTGTTT[-/C]TTCAACCCAGGAAGG	9921
rs768767968	snp	C/G			synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120546457	CAAACGTGAACTTTC[C/G]TACCCCAAAAATGAA	9921
rs768775613	in-del	-/TGT			intron-variant	RNF10	GRCh38.p7	12:120567862	GCATTTCATTATGGG[-/TGT]GTGTGTGTGTGTGTG	9921
rs768798010	snp	A/G	1.68442e-05	0.00290204	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120565507	CAGGATTGAGATAGA[A/G]GAGAACAAGAAACAG	9921
rs768884209	snp	C/T	7.10669e-05	0.00596057	intron-variant	RNF10	GRCh38.p7	12:120563314	GGAAAGCAGGAGATA[C/T]CCTTTCTGTTGACTT	9921
rs768928605	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120560682	GCTACACCATCGTGA[A/G]CTTTGAATGTTGCAT	9921
rs769045999	in-del	-/AG	1.64768e-05	0.00287021	frameshift-variant, nc-transcript-variant, intron-variant	RNF10	GRCh38.p7	12:120571264	GGGAGTCTGGAAGAA[-/AG]GACTCTCCCTTCCCT	9921
rs769082841	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120568138	TAGTCCCAGCTACTT[C/G]GGAGGCTGAGGTGGG	9921
rs769089899	snp	C/G/T	0.000147414	0.00858416	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534846	ACGCCGCCGCCACCG[C/G/T]CTCCGACATGGACAA	9921
rs769094816	in-del	-/G			intron-variant	RNF10	GRCh38.p7	12:120570564	GTACTGACCATGTGA[-/G]GGCCTGCTGCTGGGG	9921
rs769203369	snp	C/T	1.64779e-05	0.00287031	missense, synonymous-codon, nc-transcript-variant, intron-variant	RNF10	GRCh38.p7	12:120571272	TGGAAGAAGACTCTC[C/T]CTTCCCTTCCTTTGC	9921
rs769241900	in-del	-/GGGA			intron-variant	RNF10	GRCh38.p7	12:120535017	CTGCCCCTGCTGCTG[-/GGGA]GGGAGAGTCGTTGCT	9921
rs769308748	snp	C/T	6.96609e-05	0.00590132	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563598	CACACGCCTCAGCAG[C/T]TCTCCTTGTTACTAC	9921
rs769327263	snp	C/T	1.66454e-05	0.00288486	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120552688	AACAAGGAACTCTTT[C/T]TACAGGCCAAGTGAG	9921
rs769332139	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120566212	CACATGTCCTGAACT[C/T]TGAGAAAACTGATAT	9921
rs769443680	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120565340	AGTCCAGCTGGGCCT[A/C]CTGTTGTGGGTTTAG	9921
rs769488048	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120540364	AGCCAGGATTGAGAA[C/T]CACCACTCTGAGATT	9921
rs769499492	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120564962	GCACTACTGTTTCCA[A/G]CCCCAGTGCTGGCTG	9921
rs769523467	snp	A/G			missense, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575821	GTTCCTCCTGCCCCT[A/G]TGGACAGCGACGGGG	9921
rs769554847	snp	A/G	1.64966e-05	0.00287194	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557680	ATCCCATTCATCTAG[A/G]AGGTGAGTTCTTTAA	9921
rs769575341	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120573962	TCATCAGCTCTTTCA[A/G]GAATGAATGCGAGAA	9921
rs769577054	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120560014	TAAACTTCTAAACTC[A/G]AGCAATCTTCCTGTC	9921
rs769581272	snp	C/T	1.66239e-05	0.00288299	intron-variant	RNF10	GRCh38.p7	12:120560701	TGAATGTTGCATTTC[C/T]TTGATCTTGCTGGCA	9921
rs769607794	snp	C/T	1.64857e-05	0.00287099	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120546439	ATCCAAGCGTTATAA[C/T]CGCAAACGTGAACTT	9921
rs769630404	snp	C/G	1.6483e-05	0.00287076	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120560794	CTGCACCGGGTAGTT[C/G]TGGAGGAGAAAGTAG	9921
rs769645199	in-del	-/A			intron-variant	RNF10	GRCh38.p7	12:120564028	CCATCCTAAGTTCAC[-/A]AACCTTCAAGGCCTT	9921
rs769715679	snp	C/T	1.64784e-05	0.00287035	intron-variant	RNF10	GRCh38.p7	12:120563101	TTACTAAGTGGCTGC[C/T]GTTCCTCAAATGCTG	9921
rs769822261	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120565648	AACTTTTAAATGTGA[A/G]TCATGAGAGCACCTC	9921
rs769868419	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120548035	AGCAGAGAAAAGGAT[A/G]AGTAATGTTTTTGGC	9921
rs769871307	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120567636	AACCTGGGAGGCGGA[A/G]GTCTCAGTGAGACAA	9921
rs769892274	snp	A/G	1.75068e-05	0.00295857	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120565528	CAAGAAACAGGGCAA[A/G]TGTAAGTTCAGGAAC	9921
rs769905989	in-del	-/GGGGGAGTTT	3.29473e-05	0.00405864	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575711	TGGTCCACTGGTGAA[-/GGGGGAGTTT]GGCTTCTTTCCATAA	9921
rs769947156	snp	A/G	1.65304e-05	0.00287488	intron-variant	RNF10	GRCh38.p7	12:120566795	TTGAATTCTGTAAAT[A/G]GGTTTACAAGGGTTA	9921
rs769959834	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120567632	CTTGAACCTGGGAGG[C/T]GGAGGTCTCAGTGAG	9921
rs769984466	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120537904	AAACTGGATATTGGC[G/T]GATTTTTAAAGTTGA	9921
rs770014286	snp	A/G	1.64741e-05	0.00286998	missense, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575801	TTTTAGATGAGAACA[A/G]CTTAGTTCCTCCTGC	9921
rs770032656	snp	A/G	3.29484e-05	0.00405871	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557352	CAGCCAAGATAACCC[A/G]TTGTGGACACATCTT	9921
rs770071879	snp	C/T	1.65359e-05	0.00287536	intron-variant	RNF10	GRCh38.p7	12:120565062	AGTATTGGTCCTTTT[C/T]CCAATGTAGGATGTT	9921
rs770088211	snp	A/G	2.01607e-05	0.00317489	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534944	GCCTCGGCGGGGCCA[A/G]CCGGCGAGTCTAAAC	9921
rs770112141	snp	A/C	2.01558e-05	0.00317451	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534859	CGCCTCCGACATGGA[A/C]AAGAACAGCGGCTCC	9921
rs770146234	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120550086	TAGCTGCCTGCGCTA[A/G]AGAAGTAAAAAGTCC	9921
rs770294777	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120557128	TCATACATGTACCTA[C/T]GTTGTAAACAATTTT	9921
rs770349979	snp	A/G			upstream-variant-2KB	RNF10	GRCh38.p7	12:120532818	GTGAATTTCTACCCA[A/G]CCACGCCTAAACGAA	9921
rs770358034	snp	A/G	1.64727e-05	0.00286986	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563872	CTCGTGCGGGAGTAC[A/G]GCAGCCTGGAGAGGA	9921
rs770384529	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120574122	TCAAATGTCTAAACC[A/G]TAGGAGACCCAAACT	9921
rs770399439	snp	C/T	1.64746e-05	0.00287002	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120565155	GGCTTTGCAACCTCC[C/T]GTGGTCTCTAAGGAA	9921
rs770411062	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120542697	AGCTGGGATTACAGG[C/T]GTGTGGCACCACACC	9921
rs770434287	snp	A/G	3.30655e-05	0.00406591	intron-variant	RNF10	GRCh38.p7	12:120563787	GGCCAAGACTGGTGT[A/G]TGATAGAGCCCCTTG	9921
rs770446636	snp	C/T	0.000130183	0.00806688	utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534768	CCTGGGTCCCCGCCG[C/T]GCCCGCTCCGCTCCG	9921
rs770499934	in-del	-/AGG			intron-variant	RNF10	GRCh38.p7	12:120574819	TAATCCCAGCTACTC[-/AGG]AGGATGAGGCAGGAG	9921
rs770524762	snp	C/T	1.64732e-05	0.0028699	splice-donor-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575690	TGCTCCAAAGAAAGG[C/T]GAGGATGGTCCACTG	9921
rs770554243	snp	C/T	3.30732e-05	0.00406638	intron-variant	RNF10	GRCh38.p7	12:120560723	TTGCTGGCATTCTTA[C/T]AGATGAACAGCACAG	9921
rs770673532	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120535176	ATTAATACTCAAAAC[C/T]GCTCGATTAAGCAGG	9921
rs770686714	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120544184	GTGAGCCGAGATTGC[A/G]CCACTGCACTCCAGC	9921
rs770721954	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120560920	GATGCTAAACCTTTT[C/T]ACTTTCTCGGCGTTC	9921
rs770724752	in-del	-/T	3.2956e-05	0.00405918	intron-variant	RNF10	GRCh38.p7	12:120557522	CACTCCTTGCCCTGC[-/T]ACATATGAGTGTCCA	9921
rs770748090	snp	A/G	1.6661e-05	0.00288621	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546594	TTAATGGTGGAAGAC[A/G]AGATGAGGTATGGAA	9921
rs770803003	in-del	-/TT			intron-variant	RNF10	GRCh38.p7	12:120540856	GCCAGTTTACTTTCT[-/TT]TTTTTTTTTTTTTTG	9921
rs770887761	snp	A/G	1.64866e-05	0.00287106	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120566829	TTCCTTTGCAGACCC[A/G]GAAGTCCACATTCCC	9921
rs770902197	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120562468	TAGTAGAGATGGGGT[C/T]TCTCCATGTTGGTCA	9921
rs771031783	snp	A/G	1.69464e-05	0.00291083	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563355	GCAACAGGGTGTGCT[A/G]GAGTATCTGTCTGCC	9921
rs771084696	snp	A/G	1.64762e-05	0.00287016	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563452	GTAGAAGAGGAGGAA[A/G]CAGTGTCTGAACCAG	9921
rs771086821	snp	C/G	1.69654e-05	0.00291246	intron-variant	RNF10	GRCh38.p7	12:120557241	GACAGTCCCTAATCA[C/G]TTCTTCAAGCAGTGA	9921
rs771109617	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120538095	AGCTGAACACTTCAT[A/G]TACTTGATTCTGCTG	9921
rs771128580	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120565210	AATGCCCCTGCTCTG[C/T]TTCTCTTTATAGTAG	9921
rs771132242	snp	C/T	3.29462e-05	0.00405857	synonymous-codon, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575820	AGTTCCTCCTGCCCC[C/T]GTGGACAGCGACGGG	9921
rs771133862	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120569323	ACAAAGTGTCCATCA[A/T]TGGAATATTTAAAAC	9921
rs771173517	snp	G/T	0.00037154	0.0136247	intron-variant, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120539420	TGATTCTGTAGTAAG[G/T]CCATATGTTGCCCCT	9921
rs771180742	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120571047	GAACATGGAAGAGTT[C/G]AAAGTTGGATCAATG	9921
rs771189433	snp	C/T	1.64789e-05	0.0028704	synonymous-codon, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575910	TATTGAAGCAGCCTT[C/T]ATGAAACTGGACACA	9921
rs771214352	snp	A/G/T	3.29464e-05	0.00405861	intron-variant	RNF10	GRCh38.p7	12:120562908	AGTGTGTGTCTGGAA[A/G/T]CTTAACCTTCTCTGG	9921
rs771290820	in-del	-/A	1.68408e-05	0.00290175	intron-variant	RNF10	GRCh38.p7	12:120546382	GCTTCTTAAGACGTT[-/A]CTTTTGTGTTTCTTG	9921
rs771297903	snp	C/T	5.10217e-05	0.00505057	intron-variant	RNF10	GRCh38.p7	12:120565391	TAATGACCATGTTGT[C/T]CTGGGTCTACCTCTT	9921
rs771353655	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120545460	GCCTCCCAAAGTGCT[A/G]GGATTACAGGCATGA	9921
rs771408833	snp	C/T	1.64732e-05	0.0028699	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120552585	CTTGTTGAATTTCAC[C/T]TTTGAACCCCGTGGC	9921
rs771522534	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120552950	CATGTTTGGAATTGG[A/T]CCTAGATTTGAATCT	9921
rs771531270	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120562582	CCTGGCCGTATGTGT[C/T]TTTACAGTAGAATGA	9921
rs771533783	snp	A/G	1.6473e-05	0.00286988	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120562976	TGTCGGGATTGGCCG[A/G]AAGCAGAAGGGAGGT	9921
rs771579645	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120555387	GGGTTTCACCTTGTT[C/G]GCCAGGCTGTTTTTG	9921
rs771663009	snp	A/G/T	3.31808e-05	0.00407302	intron-variant	RNF10	GRCh38.p7	12:120565040	AGAGTTAGGCTTGCT[A/G/T]TTGTTGAGTATTGGT	9921
rs771702199	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120575264	GAGGGTACTACTCAC[C/T]GCTTCCTCCGACAGC	9921
rs771716293	snp	A/G	1.64855e-05	0.00287097	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120560835	GCAGCTGGCAGAGGA[A/G]AAGCACACTCCCGAG	9921
rs771718056	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120543114	TTTTCTTCTTTCTGA[A/G]GCATTGTTTAACCTT	9921
rs771743893	snp	C/G			intron-variant, splice-donor-variant	RNF10	GRCh38.p7	12:120539469	TACTCTGGATGATGG[C/G]TAAGCAACTTGCTTG	9921
rs771856939	snp	A/G	1.64806e-05	0.00287054	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120566918	CTTTGGGTCCCACCA[A/G]CACCGAGGGCCATGG	9921
rs771867119	snp	A/G	1.64749e-05	0.00287005	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120552536	AGTTTAGCCCTGCCC[A/G]GTTCTCTGGTCCTAA	9921
rs771917253	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120539200	AGTCCTGTTTCACAG[A/C]AAAGAAAATAGAGGC	9921
rs771966728	snp	A/G/T	5.01419e-05	0.00500688	synonymous-codon, missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563562	GTCCAGCCAGCAGGA[A/G/T]CCCATCACCAAGTCA	9921
rs771974880	snp	A/C	1.64836e-05	0.0028708	missense, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575926	ATGAAACTGGACACA[A/C]CAGCTACTTCAGATC	9921
rs772018040	snp	A/G	9.88549e-05	0.00702977	intron-variant	RNF10	GRCh38.p7	12:120557527	CTTGCCCTGCTACAT[A/G]TGAGTGTCCATGTTT	9921
rs772059016	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120550202	TAGCTACATGTAGCT[A/G]CTGGCTGCTGTGTTG	9921
rs772134446	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120571302	CCCAGGTAAATCCTT[A/T]GCTTGTGAAGCAGCC	9921
rs772206831	snp	C/T	1.64751e-05	0.00287007	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557412	CACTGAGTGAGAAGA[C/T]GTGGAGTAAATGTCC	9921
rs772254824	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120548647	TATGAGCTTGAGGGA[-/T]TTTTTTTTCTTTCTT	9921
rs772306886	snp	A/G	0.000371955	0.0136323	intron-variant	RNF10	GRCh38.p7	12:120539476	GATGATGGGTAAGCA[A/G]CTTGCTTGTGATTAC	9921
rs772317730	snp	A/G	1.69545e-05	0.00291152	intron-variant	RNF10	GRCh38.p7	12:120565400	TGTTGTCCTGGGTCT[A/G]CCTCTTTACAACCTG	9921
rs772335681	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120559843	TGGGATTATAGGCGC[C/T]CGTCACCACGCCCAG	9921
rs772341422	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120572406	TACGGATCTTTCTTA[C/T]GTAATTACAGCAGTT	9921
rs772358194	snp	A/G	1.64933e-05	0.00287165	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546429	ACTCCAGTGGATCCA[A/G]GCGTTATAATCGCAA	9921
rs772371029	snp	G/T	1.64727e-05	0.00286986	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563000	GGGAGGTCACTGGTG[G/T]TGTGGCTGCTCTGGA	9921
rs772389939	in-del	-/A			intron-variant	RNF10	GRCh38.p7	12:120561231	TCTTTGTTTTCTGGG[-/A]AAATACTTAAGATTC	9921
rs772470292	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120566339	AATTATGAATAGTTA[A/G]AACAAGGTTAACTAT	9921
rs772622585	in-del	-/CTT	3.29473e-05	0.00405864	intron-variant	RNF10	GRCh38.p7	12:120562915	GTCTGGAAACTTAAC[-/CTT]CTCTGGTGTTCTCTC	9921
rs772751132	snp	G/T	1.65282e-05	0.00287469	intron-variant	RNF10	GRCh38.p7	12:120571323	TGAAGCAGCCCAGGG[G/T]TATTTAACATGAACT	9921
rs772753699	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120552784	GGCTTTTTTTAAGCT[A/G]TTGTGGGAAAGAAGC	9921
rs772821419	snp	C/G	1.64746e-05	0.00287002	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557550	CCATGTTTCAGTGTT[C/G]TTGCCACAGAGTCAC	9921
rs772824781	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120540379	CCACCACTCTGAGAT[G/T]TAAAACTTCACCCAT	9921
rs772843551	snp	A/G	1.65105e-05	0.00287315	intron-variant	RNF10	GRCh38.p7	12:120571314	CTTTGCTTGTGAAGC[A/G]GCCCAGGGGTATTTA	9921
rs772852802	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120546966	TAAAATGCATATATC[C/T]ATAGTCTCAAATTTT	9921
rs772882750	snp	C/T	1.65124e-05	0.00287331	intron-variant	RNF10	GRCh38.p7	12:120557693	AGGAGGTGAGTTCTT[C/T]AAATTTTGGGGACAA	9921
rs772894842	in-del	-/GA	3.75298e-05	0.00433168	intron-variant	RNF10	GRCh38.p7	12:120535020	GCCCCTGCTGCTGGG[-/GA]GAGTCGTTGCTCTCA	9921
rs772934634	snp	G/T	1.64784e-05	0.00287035	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576673	ACCAAGTGACACTAC[G/T]GGCCCAGGCTACCTT	9921
rs772963514	snp	A/G	3.2963e-05	0.00405961	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120560822	TAGCACTAGAGCAGC[A/G]GCTGGCAGAGGAGAA	9921
rs773014777	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120548082	TACCTTTTGCTGGAA[C/T]GGAGAACATTCTTTC	9921
rs773058731	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120552991	TTGACCTTAAGTAAC[-/T]TTAACAGCTTTGAGA	9921
rs773093369	in-del	-/A			intron-variant	RNF10	GRCh38.p7	12:120567830	TAAAAAAACACCACC[-/A]CCACCACAAAACTAA	9921
rs773131270	snp	A/C	1.64754e-05	0.00287009	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546507	GTCGCTCCAGTTCAC[A/C]GAAAAGCAAGACTTT	9921
rs773150960	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120537964	AAGACCAGTGCTACT[A/G]CAGCAGATACTCAGG	9921
rs773177620	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120566594	TGGTGAAACCTCATC[-/T]CTTTAAAAATTCAAA	9921
rs773183244	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120554230	ATTTTTAGTAGAGAT[A/G]GGGTTTCACCCTGTT	9921
rs773196544	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120560079	GCCACTGCGCTGGTC[C/T]ACCATTTCTTTATTC	9921
rs773261609	snp	A/G	1.80843e-05	0.00300696	intron-variant	RNF10	GRCh38.p7	12:120565539	GCAAGTGTAAGTTCA[A/G]GAACTTTCATCTTTG	9921
rs773284974	snp	C/T	1.64762e-05	0.00287016	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120554732	GCTGCCAATTTGTGG[C/T]GTCTGAAGACCAAGA	9921
rs773314170	snp	A/G	1.64789e-05	0.0028704	intron-variant	RNF10	GRCh38.p7	12:120563102	TACTAAGTGGCTGCC[A/G]TTCCTCAAATGCTGT	9921
rs773314632	snp	G/T	1.64754e-05	0.00287009	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563923	ACTGTGGTGGAGATT[G/T]CTGGCTACTCCATGT	9921
rs773330892	snp	C/G	5.92154e-05	0.00544097	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534865	CGACATGGACAAGAA[C/G]AGCGGCTCCAACAGC	9921
rs773374838	snp	A/G	1.64749e-05	0.00287005	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575717	ACTGGTGAAGGGGGA[A/G]TTTGGCTTCTTTCCA	9921
rs773417578	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120537005	CCCAACAAGATGATA[C/T]AGAATTCTATAGTAG	9921
rs773544596	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120544468	TTAAGACCAGCCTGG[A/G]CAACAAAGGCAAACC	9921
rs773560714	snp	G/T	0.00012183	0.00780385	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534947	TCGGCGGGGCCAGCC[G/T]GCGAGTCTAAACCCA	9921
rs773615266	snp	G/T	1.64741e-05	0.00286998	intron-variant	RNF10	GRCh38.p7	12:120562905	CTAAGTGTGTGTCTG[G/T]AAACTTAACCTTCTC	9921
rs773685175	snp	C/G	4.9597e-05	0.00497956	intron-variant	RNF10	GRCh38.p7	12:120565063	GTATTGGTCCTTTTT[C/G]CAATGTAGGATGTTC	9921
rs773718834	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120562799	CCCTCAAAGTTGAGA[C/T]ATTTAAGCACCTAAT	9921
rs773771963	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120570944	GGAGTAGATTCTACC[A/G]TGACTTCTAGAGTTA	9921
rs773775702	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120543349	TTGAGAATCATTGTA[A/T]TAAGATAAAAGTGGG	9921
rs773789068	snp	C/T	1.65209e-05	0.00287405	intron-variant	RNF10	GRCh38.p7	12:120557699	TGAGTTCTTTAAATT[C/T]TGGGGACAAATAATC	9921
rs773827480	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120573281	TCAGGGCAGAATCCT[A/G]TTACTCCCTGCATTT	9921
rs773840344	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120555634	CTGGGACTACAGGCA[C/T]GCACCACCACTCCCA	9921
rs773867350	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120574219	GCATCTGCCAACACA[A/G]ACTCATCTTGAGTAA	9921
rs773876210	snp	A/G	5.00647e-05	0.00500298	intron-variant	RNF10	GRCh38.p7	12:120552459	CTATAAATCAGTGTC[A/G]TCCTAATCTGAAATA	9921
rs773895895	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120542830	AGTGCTGGGATTACA[A/G]GGAGCCACCATGCCT	9921
rs773908688	snp	A/G			downstream-variant-500B	RNF10	GRCh38.p7	12:120577945	GATCACAAGTCTCCC[A/G]CCATTCCTACTTCCT	9921
rs773954459	snp	A/T	1.67781e-05	0.00289634	intron-variant	RNF10	GRCh38.p7	12:120546605	AGACGAGATGAGGTA[A/T]GGAATTTGAGAATGT	9921
rs774021336	snp	A/G	1.65263e-05	0.00287452	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120560726	CTGGCATTCTTATAG[A/G]TGAACAGCACAGCCA	9921
rs774057953	snp	A/T	3.29451e-05	0.00405851	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563884	TACGGCAGCCTGGAG[A/T]GGAGCCCCGAGAAGA	9921
rs774064611	snp	A/C	5.57844e-05	0.00528101	intron-variant	RNF10	GRCh38.p7	12:120565548	AGTTCAGGAACTTTC[A/C]TCTTTGACTAGCACT	9921
rs774076897	snp	G/T	3.29712e-05	0.00406011	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120546535	TTTTAACAAGATGCC[G/T]CCTCAAAGGGGCGGC	9921
rs774081050	snp	C/G	1.6483e-05	0.00287076	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120566835	TGCAGACCCAGAAGT[C/G]CACATTCCCCTCGAG	9921
rs774108276	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120537135	CCCAGGAGTTCGAGA[C/T]CCTGTCCTACAAAAA	9921
rs774161483	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120538336	TGCTTCCTAGCTACA[C/T]GATTAATTTCTTTGA	9921
rs774183489	in-del	-/TT/TTT			intron-variant	RNF10	GRCh38.p7	12:120551299	CTAGTGTTTTTTTTT[-/TT/TTT]TTTTTTTTTTTTTGA	9921
rs774218292	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120562517	AACCTCAGGTGATCC[A/G]CCCACCTCAGTCTCC	9921
rs774234208	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120536787	CTCCAACTGTGAATT[C/T]TCAACTAATTTTTCT	9921
rs774240591	in-del	-/AG			intron-variant	RNF10	GRCh38.p7	12:120544638	TCTAGCCTGGGTGAC[-/AG]AGCAAAACCTTGTCT	9921
rs774293912	snp	C/T	1.65206e-05	0.00287403	intron-variant	RNF10	GRCh38.p7	12:120565213	GCCCCTGCTCTGCTT[C/T]TCTTTATAGTAGGGT	9921
rs774295571	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120567905	TATATATATGTAAAT[A/G]TATAGAAAAACTTCT	9921
rs774407546	snp	A/G	1.68937e-05	0.0029063	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563358	ACAGGGTGTGCTGGA[A/G]TATCTGTCTGCCTTC	9921
rs774431894	snp	C/T	0.000174722	0.00934507	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534874	CAAGAACAGCGGCTC[C/T]AACAGCTCCTCCGCC	9921
rs774440896	snp	A/G	1.65031e-05	0.00287251	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120560865	GTCCTGCTTTATTGA[A/G]GCAGCTATCCAGGAG	9921
rs774458732	snp	A/G	1.64765e-05	0.00287019	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563466	AGCAGTGTCTGAACC[A/G]GAGCCTGAGGGGTTG	9921
rs774462925	snp	A/G	5.06889e-05	0.00503407	intron-variant	RNF10	GRCh38.p7	12:120557252	ATCAGTTCTTCAAGC[A/G]GTGAACCTTCTGGTG	9921
rs774504407	snp	A/G	1.64789e-05	0.0028704	missense, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575911	ATTGAAGCAGCCTTC[A/G]TGAAACTGGACACAC	9921
rs774506367	snp	C/T	1.64991e-05	0.00287215	stop-gained, nc-transcript-variant	RNF10	GRCh38.p7	12:120565078	CCAATGTAGGATGTT[C/T]GACAGCGTCACAGAT	9921
rs774517961	snp	A/G	1.64741e-05	0.00286998	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557406	ATCTTTCACTGAGTG[A/G]GAAGACGTGGAGTAA	9921
rs774538765	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120555851	TGGAGTGCAGTGGCG[C/T]GATGTTGGCTCACTG	9921
rs774559334	snp	C/G	3.2969e-05	0.00405998	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120565177	TCTAAGGAAACCCTA[C/G]AGATGTTCTCAGGTG	9921
rs774593078	in-del	-/AAGT			intron-variant	RNF10	GRCh38.p7	12:120556050	TGTCTCGGCCTCCCA[-/AAGT]GTTGGGATTACAGGC	9921
rs774653774	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577506	CTGAATTTGATGTGA[A/G]TTCTTTTGCTGCTTA	9921
rs774687538	snp	A/G	4.94173e-05	0.00497053	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120562985	TGGCCGGAAGCAGAA[A/G]GGAGGTCACTGGTGT	9921
rs774728097	snp	G/T	1.65304e-05	0.00287488	intron-variant	RNF10	GRCh38.p7	12:120571160	CCCTTGGAACGTGAC[G/T]AATATAATCAGGTCT	9921
rs774742025	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120564109	TGTAAGTGAAGTGTC[C/T]CCTCAGCATGCCAGG	9921
rs774744514	snp	C/G	1.67685e-05	0.00289551	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120552696	ACTCTTTTTACAGGC[C/G]AAGTGAGTATTGCTA	9921
rs774762473	snp	A/G			upstream-variant-2KB	RNF10	GRCh38.p7	12:120533245	TTTAATAGGGTCGGG[A/G]TTTTGCTATGTTGGC	9921
rs774769340	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120569344	TATTTAAAACTTGTG[A/G]TGACCATTTTGTTCA	9921
rs774801649	snp	A/G	9.89527e-05	0.00703325	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546543	AGATGCCTCCTCAAA[A/G]GGGCGGCGGCAGCAG	9921
rs774891180	snp	C/G	1.64732e-05	0.0028699	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120552592	AATTTCACTTTTGAA[C/G]CCCGTGGCCAGACGG	9921
rs774950456	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120542735	TGTTTGTATTTCTAG[G/T]AAAGATGGGGCTTCA	9921
rs775085246	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120549314	AATGAATGGACTGCA[A/G]AAGCGTACTAGGATT	9921
rs775086175	snp	A/G	1.64852e-05	0.00287094	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120560837	AGCTGGCAGAGGAGA[A/G]GCACACTCCCGAGTC	9921
rs775104486	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120569623	GGCTCACTGCAACCT[C/T]TGCGTCCCAGGTTGA	9921
rs775106880	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120562607	GAATGATTTATATTC[C/T]TTTGGCTATATACCC	9921
rs775128899	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120539279	AGGCGGTATTTTTCA[A/G]TAAGCTTTGTATAAT	9921
rs775163649	in-del	-/AAAAAC	1.65225e-05	0.00287419	cds-indel, nc-transcript-variant	RNF10	GRCh38.p7	12:120576614	GAGGAAAGAAAAGAA[-/AAAAAC]AGAAACAGAAGCTCC	9921
rs775201689	snp	A/G	3.34169e-05	0.00408746	intron-variant	RNF10	GRCh38.p7	12:120552450	GGGTTTCTGCTATAA[A/G]TCAGTGTCATCCTAA	9921
rs775202544	snp	C/G	1.64806e-05	0.00287054	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563478	ACCAGAGCCTGAGGG[C/G]TTGCCAGAGGCCTGT	9921
rs775210109	snp	A/G	1.68136e-05	0.0028994	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563364	TGTGCTGGAGTATCT[A/G]TCTGCCTTCGATGAA	9921
rs775358397	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120550236	ATTACAGCTGTAGAA[C/T]GGAAACCTGTAGGTG	9921
rs775367992	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120571319	CTTGTGAAGCAGCCC[A/G]GGGGTATTTAACATG	9921
rs775427244	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120538491	GCTAATTGCCTGAAC[A/G]TTTATATAACATTCC	9921
rs775460531	snp	C/T			upstream-variant-2KB	RNF10	GRCh38.p7	12:120533604	TGTATGAAGAAGTGC[C/T]GTAAAGTGATATTAA	9921
rs775486963	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120567914	GTAAATGTATAGAAA[A/C]ACTTCTGTTAGAAGG	9921
rs775510927	snp	C/T	1.64939e-05	0.0028717	missense, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575944	GCTACTTCAGATCCC[C/T]TCTCTGGTAAGGGCA	9921
rs775532683	snp	C/T			upstream-variant-2KB	RNF10	GRCh38.p7	12:120533350	GTGAGCCACCACGCC[C/T]GGCTGCCCAACTAAT	9921
rs775534719	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120560634	CCCCATTTTCACCCC[A/G]GAGAAAAGGCTGTAT	9921
rs775550315	snp	C/G	1.69126e-05	0.00290792	intron-variant	RNF10	GRCh38.p7	12:120565404	GTCCTGGGTCTACCT[C/G]TTTACAACCTGACCA	9921
rs775555305	snp	C/G			downstream-variant-500B	RNF10	GRCh38.p7	12:120577778	GGAAATTTCCTGGAT[C/G]GATGAGGGTGTTCTG	9921
rs775593828	snp	C/T	6.67193e-05	0.0057754	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534967	GTCTAAACCCAAGAG[C/T]GGTAAGGACGGGCCT	9921
rs775604527	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120540039	GGGTTTCGCCATGTT[A/G]GCCAGGCTGGTCTCA	9921
rs775642665	snp	A/G	0.000186029	0.00964261	intron-variant	RNF10	GRCh38.p7	12:120539499	GTGATTACAGCATGA[A/G]TCAGCAGCAGAAACT	9921
rs775716902	snp	A/G	3.29538e-05	0.00405904	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563008	ACTGGTGTTGTGGCT[A/G]CTCTGGAACAACTGG	9921
rs775740926	snp	A/C	3.29603e-05	0.00405944	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546452	AATCGCAAACGTGAA[A/C]TTTCCTACCCCAAAA	9921
rs775743023	in-del	-/A			intron-variant	RNF10	GRCh38.p7	12:120547134	CGTTTCATACCATGC[-/A]ATTATGATAGAATAA	9921
rs775769363	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120571108	GTAATTTTCCAGACC[C/T]GACTCAGGGCTCACT	9921
rs775798866	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120566348	TAGTTAGAACAAGGT[A/T]AACTATATTAAAGAC	9921
rs775864769	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120552354	GCAGTGAGCCAAGAT[C/T]GTGCCATTGCACTCC	9921
rs775906667	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120555490	CTGGCCCAGTTGTAC[-/T]TTTTTTTTTTTTTTG	9921
rs775907906	snp	C/T	0.000124618	0.00789263	utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534776	CCCGCCGCGCCCGCT[C/T]CGCTCCGACTGCCGT	9921
rs775920963	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120557770	CAGAAAGTGAAGCCT[C/T]TGGGCAGGGCACATC	9921
rs775976699	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120565767	TAATAGTGGGTGATA[C/T]ACACCTGTTCCAGAG	9921
rs776033499	snp	A/G	1.65086e-05	0.00287298	intron-variant, missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120571172	GACGAATATAATCAG[A/G]TCTCTGGTTCCCTTT	9921
rs776078407	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120535390	GGGTGAGGGCCCAAG[A/G]ACCTTTCAAACTCAG	9921
rs776086594	snp	C/T	1.65263e-05	0.00287452	intron-variant	RNF10	GRCh38.p7	12:120571324	GAAGCAGCCCAGGGG[C/T]ATTTAACATGAACTC	9921
rs776119099	in-del	-/TC	0.000494071	0.0157096	intron-variant	RNF10	GRCh38.p7	12:120562927	AACCTTCTCTGGTGT[-/TC]TCTCTGGCCACGTTA	9921
rs776143776	snp	C/T	1.65143e-05	0.00287348	intron-variant	RNF10	GRCh38.p7	12:120563796	TGGTGTGTGATAGAG[C/T]CCCTTGTCCTCAGCG	9921
rs776149316	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120573508	AAGAGTAAAACAATT[A/C]ACATGTCAAACTATT	9921
rs776194203	snp	C/G	1.64808e-05	0.00287057	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120566942	GCCATGGGGCCCTCT[C/G]CATTTCTCCTCTCAG	9921
rs776207559	in-del	-/TCT	1.65485e-05	0.00287645	cds-indel, nc-transcript-variant	RNF10	GRCh38.p7	12:120546572	AGCAAACTCTTTAGC[-/TCT]TCTTTTAATGGTGGA	9921
rs776208742	snp	A/T			upstream-variant-2KB	RNF10	GRCh38.p7	12:120533023	CTCTGTCACTCATAC[A/T]GGAGTGCACTGGCAC	9921
rs776229441	snp	C/G	1.64749e-05	0.00287005	intron-variant	RNF10	GRCh38.p7	12:120557535	GCTACATATGAGTGT[C/G]CATGTTTCAGTGTTG	9921
rs776230652	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120539474	TGGATGATGGGTAAG[A/C]AACTTGCTTGTGATT	9921
rs776251725	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120557975	AGTCTTGGTGCCTGT[C/T]GTCAAGAAACTCAGT	9921
rs776273908	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120563795	CTGGTGTGTGATAGA[G/T]CCCCTTGTCCTCAGC	9921
rs776307567	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120551583	GGATTACAGGCATGA[A/G]CTACTATTCCTGGTC	9921
rs776365643	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120540341	CTGTGCAAGTGATTC[C/T]GGTGTGCAGCCAGGA	9921
rs776370703	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120572560	GAGATGATTAACAAG[C/T]GGCTCCCAGGAGTTA	9921
rs776426981	snp	C/G	3.40785e-05	0.00412772	intron-variant	RNF10	GRCh38.p7	12:120546362	GTTGGCTAAGTGAAT[C/G]TATCAGCTTCTTAAG	9921
rs776546474	snp	A/C/T	3.29768e-05	0.00406048	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557673	GTAGACCATCCCATT[A/C/T]ATCTAGGAGGTGAGT	9921
rs776585651	in-del	-/T	1.64806e-05	0.00287054	intron-variant	RNF10	GRCh38.p7	12:120563120	CCTCAAATGCTGTCA[-/T]TGAGCTGGTAGGCAT	9921
rs776585816	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120566434	AGACCTTTGGGGGTA[C/T]GCATGTGTGATGTCC	9921
rs776599447	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120571447	AAGTTAACTGCCTGT[C/T]GGAGCTTTATGCAGC	9921
rs776607034	snp	C/T	1.65179e-05	0.00287379	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575973	CAGAGGCTGGAGTGC[C/T]CAGGGTTGTCAAACA	9921
rs776636696	snp	A/G	1.70828e-05	0.00292252	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120565518	TAGAGGAGAACAAGA[A/G]ACAGGGCAAGTGTAA	9921
rs776639073	snp	A/G	1.66158e-05	0.0028823	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120565436	TCTGCAGATGACATT[A/G]AGAAGAGGAAACGTC	9921
rs776664164	snp	C/T	1.64773e-05	0.00287026	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120576657	CACCTCAGTCGTCCA[C/T]ACCAAGTGACACTAC	9921
rs776689837	snp	A/G	3.29495e-05	0.00405877	intron-variant	RNF10	GRCh38.p7	12:120563079	CAGGAAGGTTAGTGT[A/G]TTCCTGTTACTAAGT	9921
rs776833330	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120535555	TGAGTGAGTGCCCCG[A/G]GTTTACTTACTTGTA	9921
rs776850534	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120563317	AAGCAGGAGATATCC[-/T]TTCTGTTGACTTAGA	9921
rs776859303	snp	C/T	1.64838e-05	0.00287083	intron-variant	RNF10	GRCh38.p7	12:120554714	CTGTCTTTCCTATTT[C/T]TAGCTGCCAATTTGT	9921
rs776885129	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120536785	TTCTCCAACTGTGAA[A/T]TCTCAACTAATTTTT	9921
rs776910731	snp	C/T	1.7608e-05	0.0029671	utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534788	GCTCCGCTCCGACTG[C/T]CGTCGCCGCCGAGGC	9921
rs776955496	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120542145	TGCTGGGATTACAGG[C/T]GTGAGCCACCGTGCC	9921
rs776961489	snp	C/G			downstream-variant-500B	RNF10	GRCh38.p7	12:120577984	GGCAGTCTGACTTGT[C/G]TTCAGGGCGCCTTGT	9921
rs777004659	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120543186	ACCAAGAAATAATTT[C/T]TTCTAAGTTTAAAAA	9921
rs777123614	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120567184	CTGCCAGCTTCTAAG[A/C]ACCTCAAGGAGCTCT	9921
rs777183097	in-del	-/T	3.29554e-05	0.00405914	intron-variant	RNF10	GRCh38.p7	12:120557481	GGTGAGATTGAGACA[-/T]TTACTCAGTTAGATC	9921
rs777194595	snp	C/T	1.78902e-05	0.00299078	intron-variant	RNF10	GRCh38.p7	12:120563298	TTGCCACATTGCTTT[C/T]GGAAAGCAGGAGATA	9921
rs777253684	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120567598	CCCAGCTACTTGGGA[C/G]GCTGAGGCAACAGAA	9921
rs777259128	snp	G/T	8.23608e-05	0.00641667	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563902	AGCCCCGAGAAGATC[G/T]CAGCAACTGTGGTGG	9921
rs777259411	in-del	-/C	3.29739e-05	0.00406028	intron-variant	RNF10	GRCh38.p7	12:120575605	CTACTTAAATTCTCT[-/C]CCCCACTTCTTTCCC	9921
rs777266663	snp	C/T	1.64732e-05	0.0028699	synonymous-codon, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575678	GTGGCCCAAAACTGC[C/T]CCAAAGAAAGGTGAG	9921
rs777281124	snp	A/G	6.5912e-05	0.00574035	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120554802	CTGGGACTTTGTGGA[A/G]CAAGTGGTGAGTAGC	9921
rs777282213	in-del	-/ATAG	1.65293e-05	0.00287479	intron-variant	RNF10	GRCh38.p7	12:120565218	GCTCTGCTTCTCTTT[-/ATAG]ATAGTAGGGTTCAGG	9921
rs777431974	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120536527	CTGCTGGATATGGCA[A/G]ACTTGTTTACCTGGT	9921
rs777484709	snp	C/T	9.96231e-05	0.00705703	intron-variant	RNF10	GRCh38.p7	12:120560707	TTGCATTTCTTTGAT[C/T]TTGCTGGCATTCTTA	9921
rs777508213	snp	C/T	1.64757e-05	0.00287012	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575746	CATAAAAGGCTGTTT[C/T]TAGAAAAAGAGTTGT	9921
rs777564095	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120562422	AGGAATTACAGGCAT[G/T]CCCCACCATGCCTGG	9921
rs777589612	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120574816	CTATAATCCCAGCTA[C/T]TCAGGAGGATGAGGC	9921
rs777620025	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120545449	CGCCCACCTCGGCCT[A/C]CCAAAGTGCTAGGAT	9921
rs777680870	snp	A/G	1.6483e-05	0.00287076	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120560823	AGCACTAGAGCAGCA[A/G]CTGGCAGAGGAGAAG	9921
rs777740003	snp	A/G	1.65831e-05	0.00287945	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546582	TTAGCTCTTCTTTTA[A/G]TGGTGGAAGACGAGA	9921
rs777761444	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120543979	ATGCCTGTAATCCCA[C/G]TACTTTGGGAGGCCG	9921
rs777793143	snp	A/G	8.25239e-05	0.00642302	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120552499	TCTCATTCTCTCTAG[A/G]TAGCAGAGGCTCAAC	9921
rs777902220	snp	A/C			intron-variant	RNF10	GRCh38.p7	12:120548953	GGGATTACAGGCATG[A/C]GCCACCGCGCCCGGC	9921
rs777935114	snp	A/T	0.000543662	0.0164783	intron-variant	RNF10	GRCh38.p7	12:120557510	TCCCAATCTCTTCAC[A/T]CCTTGCCCTGCTACA	9921
rs777935936	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576793	CTCTGGGGGGAGGGG[A/G]TTTCCACAATGTGAG	9921
rs777946550	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120538912	GTAAATGGACCTGGA[G/T]ATTTTAATGGCTTTG	9921
rs778043432	snp	A/C			utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534753	CCTGAACGCCATGAG[A/C]CTGGGTCCCCGCCGC	9921
rs778055418	snp	G/T	3.29533e-05	0.00405901	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120566899	ACCTGCTCCTCTGAT[G/T]CTGCTTTGGGTCCCA	9921
rs778079330	snp	C/G	1.64735e-05	0.00286993	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557374	ACACATCTTCTGCTG[C/G]GCATGCATCCTGCAC	9921
rs778110394	snp	C/G	1.6477e-05	0.00287024	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563430	TAGACCTCTTGCTCT[C/G]CCTCTGGTAGAAGAG	9921
rs778113513	snp	A/C	1.64795e-05	0.00287045	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120565165	CCTCCTGTGGTCTCT[A/C]AGGAAACCCTAGAGA	9921
rs778129951	snp	C/T	0.000186619	0.00965789	intron-variant	RNF10	GRCh38.p7	12:120539351	CCTGATACCACCTCT[C/T]TCTTCCTTTCATTCA	9921
rs778161611	snp	A/G	4.95487e-05	0.00497714	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563524	GCAGATGACAATCTT[A/G]AAGAGGGGACCATTT	9921
rs778172112	snp	C/T	1.6477e-05	0.00287024	synonymous-codon, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575898	CTTCAGCCAAGCTAT[C/T]GAAGCAGCCTTCATG	9921
rs778228394	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120559637	ATCCGCCTACCTCAG[C/T]CTCCCAAAGTGCTGG	9921
rs778236106	in-del	-/G			intron-variant	RNF10	GRCh38.p7	12:120539703	AACAACTGAGAAGCT[-/G]GGTTAAGTTTTTAAG	9921
rs778239776	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120538060	ATAATCCCATAAAAA[G/T]ATTTCTGCAGTATCT	9921
rs778295631	snp	A/C	1.89968e-05	0.00308189	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534915	GCAGCAAAGGGCAAC[A/C]GCCGCCCCGCTCCGC	9921
rs778352149	snp	C/T	3.29522e-05	0.00405894	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120557328	CAATATGCCTCTATC[C/T]ACCTACTGCAGCCAA	9921
rs778373688	snp	A/G	1.70162e-05	0.00291682	intron-variant	RNF10	GRCh38.p7	12:120565384	GAGGAGGTAATGACC[A/G]TGTTGTCCTGGGTCT	9921
rs778378995	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120555072	CCTTACCCTCCTGAT[C/T]TGGGTTGGGCTCATT	9921
rs778387833	snp	C/G	3.33572e-05	0.00408381	intron-variant	RNF10	GRCh38.p7	12:120546394	CGTTCTTTTGTGTTT[C/G]TTGCTTTCAGATGGA	9921
rs778443357	snp	G/T	3.58841e-05	0.00423565	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534836	AGCTCCCCCAACGCC[G/T]CCGCCACCGCCTCCG	9921
rs778448828	snp	A/G	1.64841e-05	0.00287085	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120560832	GCAGCAGCTGGCAGA[A/G]GAGAAGCACACTCCC	9921
rs778449623	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120575126	TGCCTGTAATCCCAG[C/G]TACTTGGGAGGCTGA	9921
rs778514412	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120564149	AATCAGTTAATGCTG[-/T]TCCCTGCTTCTCTGG	9921
rs778623327	snp	C/T	0.000263561	0.0114765	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575763	AGAAAAAGAGTTGTT[C/T]CTATAGTTTTAACAC	9921
rs778674747	snp	C/T	1.65007e-05	0.00287229	intron-variant	RNF10	GRCh38.p7	12:120563994	CAGTATTAACCTAAT[C/T]TCTTTGAGGTAGGCC	9921
rs778678856	snp	C/T	0.000115307	0.00759211	missense, downstream-variant-500B, nc-transcript-variant	RNF10	GRCh38.p7	12:120575854	AGTGATAATTCAGAC[C/T]GTGTTCCTGTGCCCA	9921
rs778707735	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120550062	CCATGTGTGTAATCA[C/T]ACATTTTCTAGCTGC	9921
rs778733829	snp	A/G	1.64754e-05	0.00287009			GRCh38.p7	12:120565110	TCTCTCTCACTTGCC[A/G]CTCACCTGTGAGTTC	9921
rs778753346	snp	A/G	4.94246e-05	0.0049709			GRCh38.p7	12:120552629	TTGAAGGCAGTGGAC[A/G]TGGTAGCTGGGGAAA	9921
rs778768175	snp	C/T			upstream-variant-2KB	RNF10	GRCh38.p7	12:120532406	ACAGGTGTGAGCCAC[C/T]GTGCCCGGCCCCATA	9921
rs778798355	snp	C/G	3.32917e-05	0.0040798	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563553	TTGCACTGAGTCCAG[C/G]CAGCAGGAACCCATC	9921
rs778892876	snp	A/G	1.64849e-05	0.00287092	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120552515	TAGCAGAGGCTCAAC[A/G]GGCAGAGTTTAGCCC	9921
rs779008208	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120540659	CCCTTAGGTAACTGG[A/G]AGACGAGAAACGAGT	9921
rs779047386	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120550907	GGCCCAGAATGCGGC[A/G]TTATTTTTAAGCTTG	9921
rs779057805	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120549172	GAAGGCCTGGTGATG[A/G]AGGTGGGTTCGGAGG	9921
rs779108278	snp	C/T	1.72353e-05	0.00293553	intron-variant	RNF10	GRCh38.p7	12:120576583	GTCTTTCTGTGTCTC[C/T]CTTTAGAAGAGAAAG	9921
rs779188232	snp	C/G	1.84483e-05	0.00303707	intron-variant	RNF10	GRCh38.p7	12:120563643	GGGTGCCGGAAGAGA[C/G]GGCTGGGTTGCCGCA	9921
rs779203338	snp	G/T	0.000165145	0.00908543	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576704	CTCCATCTGGTTTTT[G/T]TTTTTGTTTTTTTTT	9921
rs779307410	snp	C/T	1.69968e-05	0.00291515	intron-variant	RNF10	GRCh38.p7	12:120565393	ATGACCATGTTGTCC[C/T]GGGTCTACCTCTTTA	9921
rs779326232	in-del	-/AAA			intron-variant	RNF10	GRCh38.p7	12:120566762	GTGAGACCCCATCTC[-/AAA]AAAAAAAAAAAAAAA	9921
rs779328858	snp	A/T	0.00222717	0.033296	intron-variant, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120539443	TTGCCCCTCTGGAGG[A/T]GCTTGTCAACTACTC	9921
rs779355188	in-del	-/GA	1.64762e-05	0.00287016	intron-variant	RNF10	GRCh38.p7	12:120557529	TGCCCTGCTACATAT[-/GA]GTGTCCATGTTTCAG	9921
rs779356543	snp	C/T	3.34119e-05	0.00408715	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120565490	GAACGCCGCCGAGAG[C/T]GCAGGATTGAGATAG	9921
rs779371937	snp	C/G			intron-variant	RNF10	GRCh38.p7	12:120547649	AATAGCACATGCAAG[C/G]GACGGGAGGTGGTAG	9921
rs779384041	snp	A/C	4.96175e-05	0.00498059	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546410	TTGCTTTCAGATGGA[A/C]AGAACTCCAGTGGAT	9921
rs779437760	snp	C/T			utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534409	GCCTCGGCCCAGGGG[C/T]GAGTATCCGTTGCTG	9921
rs779439179	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120544236	TAAAAACAAAAAAAA[-/T]GATAAACCAGGCATG	9921
rs779493764	snp	A/C	1.64738e-05	0.00286995	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563061	GGAGTCTGTTTTTCA[A/C]CCCAGGAAGGTTAGT	9921
rs779500831	snp	A/G	2.93569e-05	0.00383114	intron-variant	RNF10	GRCh38.p7	12:120534995	CCTGCGGCAGTGGGC[A/G]GGGGCGACTGCCCCT	9921
rs779503141	in-del	-/TTTTTTTTT			intron-variant	RNF10	GRCh38.p7	12:120551291	GCGCCCATCCTAGTG[-/TTTTTTTTT]TTTTTTTTTTTTTGA	9921
rs779619508	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120544183	AGTGAGCCGAGATTG[C/T]GCCACTGCACTCCAG	9921
rs779646928	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120538881	GGTAATCTGCCTTGA[A/G]GAATGCCTCTGAGCT	9921
rs779657168	snp	G/T	1.64735e-05	0.00286993	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120565143	CATCTGTGAACTGGC[G/T]TTGCAACCTCCTGTG	9921
rs779712060	snp	A/G			downstream-variant-500B	RNF10	GRCh38.p7	12:120577835	GCCAGAATCACCAGT[A/G]TTTCTGTTAAATGTG	9921
rs779849179	snp	A/G	1.6546e-05	0.00287624	intron-variant	RNF10	GRCh38.p7	12:120565233	TATAGTAGGGTTCAG[A/G]GATTCTTGTGGCTAG	9921
rs779855080	in-del	-/CGCCGC	4.19437e-05	0.00457931	cds-indel, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534831	GCTGAGCTCCCCCAA[-/CGCCGC]CGCCGCCGCCACCGC	9921
rs779856247	snp	A/G	1.64773e-05	0.00287026	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120552644	ATGGTAGCTGGGGAA[A/G]GAGGAACAAGTGGGG	9921
rs779878425	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120551186	AGACATGGGATCCCT[G/T]TGTTGTCTAGACTGG	9921
rs779883047	snp	G/T	1.86827e-05	0.0030563	intron-variant	RNF10	GRCh38.p7	12:120563662	TGGGTTGCCGCAGAG[G/T]TGTTTCAGAGGTGAC	9921
rs779883738	snp	C/T	1.67033e-05	0.00288987	intron-variant	RNF10	GRCh38.p7	12:120567026	ATCAGTTAGACCTTA[C/T]GCAAAGCTTTGGTGT	9921
rs779934312	snp	A/G	1.64735e-05	0.00286993	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120557609	GATGCAGCTGATGAA[A/G]AGGGAGAAAGGGGTG	9921
rs779973223	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120559887	TTTTTAATAGAAACA[A/G]GGTATCTCTATGTTG	9921
rs779974333	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120565964	GTTGGATTTAAGAGA[G/T]CTTTCGTAGCAGTAA	9921
rs780164791	snp	C/T	1.64735e-05	0.00286993	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120563851	CACCCTGTGAATGTG[C/T]GCTGCCTCGTGCGGG	9921
rs780206246	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120572419	TATGTAATTACAGCA[A/G]TTTGTACTGAGAAAT	9921
rs780228013	snp	A/G	8.54244e-05	0.0065349	intron-variant	RNF10	GRCh38.p7	12:120565581	TGTACGTCGTTGTAT[A/G]GAACTCTGTGTCTGG	9921
rs780304232	in-del	-/CTT	1.65844e-05	0.00287957	intron-variant	RNF10	GRCh38.p7	12:120571140	TCTCTCTTGTTAAGG[-/CTT]ACACCCCTTGGAACG	9921
rs780335704	snp	A/C	1.64741e-05	0.00286998	synonymous-codon, nc-transcript-variant	RNF10	GRCh38.p7	12:120563065	TCTGTTTTTCAACCC[A/C]GGAAGGTTAGTGTGT	9921
rs780462991	snp	G/T	1.64768e-05	0.00287021	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546477	CCAAAAATGAAAGTT[G/T]TAACAACCAGTCCCG	9921
rs780489515	in-del	-/A			intron-variant	RNF10	GRCh38.p7	12:120562004	GTCAGATTCTCTTTT[-/A]TTTTTTTTAACTTTT	9921
rs780538476	snp	A/G	1.77963e-05	0.00298292	intron-variant	RNF10	GRCh38.p7	12:120563310	TTTCGGAAAGCAGGA[A/G]ATATCCTTTCTGTTG	9921
rs780583381	snp	C/G	6.59402e-05	0.00574158	intron-variant	RNF10	GRCh38.p7	12:120554823	GGTGAGTAGCTCAGC[C/G]AAGCCCATAAGCTAT	9921
rs780609992	in-del	-/T	9.69885e-05	0.00696311	intron-variant	RNF10	GRCh38.p7	12:120534981	CGGTAAGGACGGGCC[-/T]TGCGGCAGTGGGCGG	9921
rs780637406	in-del	-/AA			intron-variant	RNF10	GRCh38.p7	12:120566763	TGAGACCCCATCTCA[-/AA]AAAAAAAAAAAAAAA	9921
rs780710417	snp	A/G	1.64732e-05	0.0028699	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120575691	GCTCCAAAGAAAGGT[A/G]AGGATGGTCCACTGG	9921
rs780728165	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120536362	TCAAGGAAGTTGAGG[C/T]TGCGGTGAGCTATAT	9921
rs780743480	snp	G/T	1.64751e-05	0.00287007	missense, synonymous-codon, nc-transcript-variant, intron-variant	RNF10	GRCh38.p7	12:120571257	TCTGCGTTGGGAGTC[G/T]GGAAGAAGACTCTCC	9921
rs780837999	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120546122	TACAAGGACAGTGGT[G/T]AAGCTGTGTAAAGTA	9921
rs780875958	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120566079	AACACAAGGAACTGA[A/G]TCCTTGGCCCAGAAA	9921
rs780908036	snp	C/T	1.66153e-05	0.00288225	intron-variant	RNF10	GRCh38.p7	12:120563760	GGAGGGGTGGGGAGC[C/T]TCCTGGGGACTGGCC	9921
rs780952895	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577374	GTTTTCAGTGACTGG[C/T]TTGAGTCATAGGAGG	9921
rs780985497	snp	A/G	1.64746e-05	0.00287002	splice-acceptor-variant	RNF10	GRCh38.p7	12:120575630	TTTCCCACTTTGGCA[A/G]ATGCTGAGGGTTGGA	9921
rs780988278	snp	C/G	1.65272e-05	0.0028746	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120552675	ACATAAGCCTTTTAA[C/G]AAGGAACTCTTTTTA	9921
rs781006129	snp	A/T			intron-variant	RNF10	GRCh38.p7	12:120574147	CAAACTCCTAGAGAC[A/T]AAGGGAGAAGTTCAC	9921
rs781041511	snp	C/T	5.54472e-05	0.00526503	intron-variant	RNF10	GRCh38.p7	12:120552743	GAAAGTAGGACTCTC[C/T]GGATAGCTGTGGTGC	9921
rs781090142	in-del	-/CCTT	3.36723e-05	0.00410305	intron-variant	RNF10	GRCh38.p7	12:120557257	TCTTCAAGCAGTGAA[-/CCTT]CCTTCTGGTGGCATT	9921
rs781091268	snp	A/G	1.6477e-05	0.00287024	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546492	TTAACAACCAGTCCC[A/G]TCGCTCCAGTTCACA	9921
rs781157507	snp	C/T	3.32806e-05	0.00407912	intron-variant	RNF10	GRCh38.p7	12:120560690	ATCGTGAGCTTTGAA[C/T]GTTGCATTTCTTTGA	9921
rs781174798	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120542430	AAGTGTTGAGACAAC[C/T]GGCATGAGCCACCAA	9921
rs781211899	snp	A/G			missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120552662	GGAACAAGTGGGGAC[A/G]TAAGCCTTTTAACAA	9921
rs781241339	in-del	-/TG			intron-variant	RNF10	GRCh38.p7	12:120535846	TACCTCTGTTTTCAC[-/TG]TGCCAGTCACTGACT	9921
rs781279361	snp	A/G	0.000414422	0.0143889	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577240	TTAATGGAGTAGGCT[A/G]TCCTTGGCACTTGCA	9921
rs781287814	in-del	-/CAA			intron-variant	RNF10	GRCh38.p7	12:120567700	AGCGAGACTTTGTCT[-/CAA]AAAAAAAAAAAAAAA	9921
rs781313153	in-del	-/TGTT			intron-variant	RNF10	GRCh38.p7	12:120568776	CTACTGTGCCCAGCC[-/TGTT]TGTTTTTAAGAGATA	9921
rs781337403	snp	A/C/T	8.33346e-05	0.00645455	intron-variant	RNF10	GRCh38.p7	12:120560683	CTACACCATCGTGAG[A/C/T]TTTGAATGTTGCATT	9921
rs781364919	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120548921	GTGATCCGCCCGCTT[C/T]GGCCTCCCAAAGTGC	9921
rs781382303	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120568964	CTGATTTCTCAGGCA[C/T]TCTTGTTTTGTTTTG	9921
rs781463397	snp	A/C	1.65616e-05	0.00287759	missense, nc-transcript-variant	RNF10	GRCh38.p7	12:120546576	AACTCTTTAGCTCTT[A/C]TTTTAATGGTGGAAG	9921
rs781501757	snp	A/G	1.72421e-05	0.00293611	synonymous-codon, intron-variant, nc-transcript-variant	RNF10	GRCh38.p7	12:120563343	TTAGAGTTTGCTGCA[A/G]CAGGGTGTGCTGGAG	9921
rs781534090	snp	A/C/G	6.62312e-05	0.00575431	intron-variant	RNF10	GRCh38.p7	12:120566789	AAAAAATTGAATTCT[A/C/G]TAAATGGGTTTACAA	9921
rs781687166	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120538832	GCCCTGGCATTCTTC[C/T]TGTTATTCTGGTACC	9921
rs781692478	snp	A/G	3.99186e-05	0.0044674	missense, utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534938	CGCTCCGCCTCGGCG[A/G]GGCCAGCCGGCGAGT	9921
rs796066365	in-del	-/TTTTTTTTTTTTTTT			intron-variant	RNF10	GRCh38.p7	12:120559185	ACTACTCTTTTTTTT[-/TTTTTTTTTTTTTTT]GAGACGGAGTCTTGC	9921
rs796068684	in-del	-/GTG			intron-variant	RNF10	GRCh38.p7	12:120569341	GAATATTTAAAACTT[-/GTG]GTGACCATTTTGTTC	9921
rs796164645	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120550365	GTCAGAGAAAGTGAC[A/G]GTGGGCCAGCTAGGA	9921
rs796351487	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120555686	TTTTTAGTAGAGATG[G/T]GGTTTCTCCATGTTG	9921
rs796380932	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120548749	ACTGCAACCTCCGCT[C/T]TTGGGTTCACGCCAT	9921
rs796394368	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120566603	CTCATCTCTTTAAAA[A/G]TTCAAAAAATTAGCT	9921
rs796434473	in-del	G/TTTT			intron-variant	RNF10	GRCh38.p7	12:120540861	TTACTTTCTTTTTTT[G/TTTT]TTTTTTGAGACAGAG	9921
rs796454551	in-del	-/T			downstream-variant-500B	RNF10	GRCh38.p7	12:120577875	TTCAGTCTCATCCAT[-/T]GTATTATGGAGAAAA	9921
rs796596224	in-del	-/A			upstream-variant-2KB	RNF10	GRCh38.p7	12:120534005	GAGCGACTCCGCCTC[-/A]AAAAAAAAAAAAAAG	9921
rs796619503	in-del	-/T			intron-variant	RNF10	GRCh38.p7	12:120555491	CTGGCCCAGTTGTAC[-/T]TTTTTTTTTTTTTGA	9921
rs796841180	in-del	-/AAAAA			intron-variant	RNF10	GRCh38.p7	12:120540079	CCTCATGAGGAACTT[-/AAAAA]AAAAAAAAATAGGGG	9921
rs796909484	in-del	-/TC			intron-variant	RNF10	GRCh38.p7	12:120562270	TTCTTTTTCTTTCTT[-/TC]TTTTTTTTTTTTTTT	9921

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