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

HERC1

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs75420351	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63752141	TAATGTAATGATGAA[C/T]AGCTTGAAGATTTTT	8925
rs75450391	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63787990	AAAAAAAAGACAAAA[A/C]AAAACAAAAAACCTT	8925
rs75464731	snp	C/T	0.0655868	0.168795	intron-variant	HERC1	GRCh38.p7	15:63678923	ACCTGACACTAATAA[C/T]AGCATCTGTCTCCTA	8925
rs75467798	snp	C/T	0.0225271	0.103711	intron-variant	HERC1	GRCh38.p7	15:63642948	CATTTGATATAACTA[C/T]AATATTACCTTTGAT	8925
rs75471694	snp	C/T	0.0566069	0.158427	intron-variant	HERC1	GRCh38.p7	15:63705516	TGAAAATGAAAAAAT[C/T]ATGTGTGCATTGCTT	8925
rs75480383	snp	C/G	0.0966517	0.197444	intron-variant	HERC1	GRCh38.p7	15:63803131	GATCGCTTAAGCCTA[C/G]GAGGCTGCAGTGAGC	8925
rs75509131	snp	C/G	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63759546	CTTATCTTAACTTCA[C/G]ATTTCTTTATTGTTA	8925
rs75517236	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63825951	TTTTTTTAGTAGAGA[A/C]GGGGTTTCACCATGT	8925
rs75547633	snp	A/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63790578	GCAAGACTCCGTCTC[A/T]AAAAAAAATTTTTTT	8925
rs75593412	snp	A/C	0.00835141	0.0640778	intron-variant	HERC1	GRCh38.p7	15:63656605	ACAAAGTAAAACAGG[A/C]ATGTTCACAAAGCAT	8925
rs75604699	snp	A/T	0.0138799	0.0821421	intron-variant	HERC1	GRCh38.p7	15:63830954	AGAAAATGCTAGCAG[A/T]TGTGACCTTCCTGGC	8925
rs75638392	snp	A/G	0.00386776	0.0438055	intron-variant	HERC1	GRCh38.p7	15:63746879	ATCTCAGAGAAAGAC[A/G]TGGTTTGAGATACAG	8925
rs75641301	snp	C/T	0.0655868	0.168795	intron-variant	HERC1	GRCh38.p7	15:63667536	ATGAATTAGAAGATA[C/T]AGCTATAAAAACTAT	8925
rs75651205	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63831886	CATGCAACATCAGGG[C/T]GCCTGCATTGGAAAT	8925
rs75662856	snp	A/G	0	0	intron-variant	HERC1	GRCh38.p7	15:63824845	CAAGTCAGACGTAGG[A/G]AAAAAAAAAAACACT	8925
rs75663391	snp	G/T	0.499859	0.0083854	intron-variant	HERC1	GRCh38.p7	15:63618234	catatggctagccag[G/T]tttcccagcaccatt	8925
rs75685587	snp	C/G	0.0414363	0.137845	intron-variant	HERC1	GRCh38.p7	15:63763771	CCTAGGTACATATTA[C/G]AAGGGTATTTATTTT	8925
rs75691465	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63626767	ATACAAACTCACTTC[A/G]GTTTCCTGTAAATAA	8925
rs75713882	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63616003	AAATACGGCACAGCA[A/G]TAACAAACTCACAAT	8925
rs75714572	in-del	-/CAA			intron-variant	HERC1	GRCh38.p7	15:63809789	CCTTGTTTAGAATAG[-/CAA]AAAAAAAAAAAAAAG	8925
rs75770778	snp	A/T	0.455024	0.143057	intron-variant	HERC1	GRCh38.p7	15:63739920	AGCATATTTTATTTT[A/T]TTTTTTTTCAGACAG	8925
rs75778032	snp	C/G	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63826044	CTGGAACTAACAGGT[C/G]TGAGCCACCACGCCC	8925
rs75781755	snp	A/G	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63796724	TGGACAACTTGAAGC[A/G]GAAGCTTTCAGGTCA	8925
rs75866427	snp	A/G	0.02016	0.0983543	intron-variant	HERC1	GRCh38.p7	15:63832233	AATACATCTTAACTC[A/G]CTTCCAAGATATATA	8925
rs75894300	snp	A/G	0.030278	0.119257	downstream-variant-500B, utr-variant-3-prime	HERC1, FBXL22	GRCh38.p7	15:63608566	GCTAATGTCTGCCTC[A/G]ATGGTAACCCCTAGT	8925
rs75897756	snp	A/G	0.0648419	0.167978	intron-variant	HERC1	GRCh38.p7	15:63688325	CTCACTAGGAGGCTG[A/G]GAAAGCCTGGGGGAA	8925
rs75902347	snp	A/G	0.0456336	0.143994	intron-variant	HERC1	GRCh38.p7	15:63726818	AAAAGAAAGTTCCGC[A/G]TTCATGTTATGAGAT	8925
rs75914275	snp	A/C	0.0670745	0.170406	intron-variant	HERC1	GRCh38.p7	15:63649655	GTATTTTTAAAAGCA[A/C]ATGCCAAAAAGCTAA	8925
rs75946507	snp	A/C	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63760436	GCAGAGACACCATCC[A/C]AAAAAAAAAAAAAAA	8925
rs75962830	snp	A/G	0.108402	0.206034	intron-variant	HERC1	GRCh38.p7	15:63817400	AAAGGTAAACATTAC[A/G]TATGTCAAGGATTTG	8925
rs76062349	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63630271	ATTGTTTTAAACCAT[A/G]GTATAATACTTCTTT	8925
rs76073539	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63673723	GATATCAGAATACTA[C/T]GTATTTTGGTTTGTT	8925
rs76075647	snp	A/T	0.021333	0.101051	intron-variant	HERC1	GRCh38.p7	15:63674238	TGACCAAAAAAAAAA[A/T]TTTTTTTTTTTTACA	8925
rs76114496	snp	C/G/T	0.0107913	0.0726592	synonymous-codon	HERC1	GRCh38.p7	15:63669656	AGTCTGTGCCCGACG[C/G/T]GTGGGAAGTACAGTG	8925
rs76128558	snp	A/G	0.0252325	0.109451	intron-variant	HERC1	GRCh38.p7	15:63817395	ATCTGAAAGGTAAAC[A/G]TTACGTATGTCAAGG	8925
rs76143796	snp	A/C	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63825747	TTCATTAGAAAACCA[A/C]GAAAAAAAAGAAAAA	8925
rs76189419	snp	C/T	0.0626037	0.165477	intron-variant	HERC1	GRCh38.p7	15:63683701	TTACCCAGGCTGGCA[C/T]GCAGTAGTGTAAACA	8925
rs76198318	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63801007	AACCAAGCCTACGTA[A/T]TGCAGCTTCCATAAA	8925
rs76205041	snp	A/C	0.00121338	0.0246012	missense	HERC1	GRCh38.p7	15:63674411	GATCTGGAACGAGCG[A/C]AAGCCATGATCTATA	8925
rs76226628	snp	G/T	0.02016	0.0983543	intron-variant	HERC1	GRCh38.p7	15:63767555	TACAAAATTTTAGCC[G/T]GGCGTGGTGGCGGGC	8925
rs76227313	snp	C/T	0.0142736	0.0832652	intron-variant	HERC1	GRCh38.p7	15:63806592	TGTCCCTTTCAGCCA[C/T]TGGCACCCTAGCTTT	8925
rs76276065	snp	C/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63705327	CCTAGCTTTTTTTTT[C/T]CTTTTTGGCAGAGAC	8925
rs76276503	snp	C/G	0.00676609	0.0577691	intron-variant	HERC1	GRCh38.p7	15:63828815	TAAGATTAAACTAAA[C/G]GGAGTGGTAAAGAAA	8925
rs76283802	snp	A/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63630807	ACGTTCTGAATAAAT[A/T]AAAAGTGTGAAGCTG	8925
rs76285931	snp	A/G	0.0547245	0.156101	intron-variant	HERC1	GRCh38.p7	15:63642831	CTAAATAGTTGCACT[A/G]TTTTGGACAAGTAGT	8925
rs76319278	snp	A/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63723549	TTCTCCAAAAGGATG[A/T]GACACTCTACCAATT	8925
rs76321761	snp	G/T	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63820979	AATTCAAGTTTTGTT[G/T]TCACATATTACTTAG	8925
rs76398865	snp	C/T	0.0414363	0.137845	intron-variant	HERC1	GRCh38.p7	15:63685596	GTTGGTTAATGAGAT[C/T]TGTTGTAACTGGCTA	8925
rs76415338	snp	G/T			missense	HERC1	GRCh38.p7	15:63659783	GTGGCTGTGACCATT[G/T]CTACTGATGCTCCCA	8925
rs76418665	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63610052	CCCTATCCCTCCTTG[A/C]AAACATAACTATTTT	8925
rs76428965	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63733505	TGACAATTACTTATT[C/T]TAATGTTCAAAATAA	8925
rs76441772	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63719295	GAGCAGAGATCTAAA[C/T]GAAGTGGGGGAAAAA	8925
rs76450208	snp	C/T	0.0622301	0.165053	intron-variant	HERC1	GRCh38.p7	15:63743242	TCTGTGTATTTTCTT[C/T]TTTTTTCTTTTTTTC	8925
rs76453046	snp	C/T	0.444533	0.157025	intron-variant	HERC1	GRCh38.p7	15:63619453	gatattggtctaaaa[C/T]tctctttttttgttg	8925
rs76465062	snp	A/G	0.0154056	0.086403	synonymous-codon	HERC1	GRCh38.p7	15:63616448	ATGGAAACTCTCCTC[A/G]GTAATCCCACTGTCT	8925
rs76470154	snp	C/T	0.0689305	0.172377	intron-variant	HERC1	GRCh38.p7	15:63706560	AACTCCTAAACATTC[C/T]CAGATTTTTAAAGCG	8925
rs76478061	snp	C/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63681602	TTAAAAAAAAAAAAA[C/T]TTCCCCTACGTGATA	8925
rs76530403	snp	C/G	0.0715223	0.175059	intron-variant	HERC1	GRCh38.p7	15:63675416	ACAGGAAATATTTTA[C/G]ACTCTGCAGGGCACA	8925
rs76535505	snp	A/G	0.0667028	0.170006	intron-variant	HERC1	GRCh38.p7	15:63778414	TAAAGCAGAAGGCAC[A/G]GTTTAAGACAGCAGG	8925
rs76537165	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63611064	GGCTTATAGGATGAG[A/T]AAGTGCTTGCCAGAG	8925
rs76537198	snp	A/G	0.0599851	0.162463	intron-variant	HERC1	GRCh38.p7	15:63829735	CTTGGAGAAGTAGTC[A/G]ACTCCAGGACTGGTG	8925
rs76538038	snp	A/G	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63703928	TCTCAAAAAAAAAAA[A/G]GAAAGAAAAAAAAAG	8925
rs76543697	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63670815	ATACCAGCATACTTT[A/G]GGAGGCTGAGGCCAC	8925
rs76574278	snp	C/T	0	0	intron-variant	HERC1	GRCh38.p7	15:63692979	TGGTCAGTCTGGTCT[C/T]GAACTCCCGACCTCA	8925
rs76630268	snp	C/T	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63785873	TCAGAGAGATTATTC[C/T]TCTTTTTCTTTTTTA	8925
rs76640183	snp	A/G	0.0479149	0.147179	intron-variant	HERC1	GRCh38.p7	15:63804764	CAATAAGAAAACTCA[A/G]TTTTTAAAATGAGCA	8925
rs76645912	snp	G/T	0	0	intron-variant	HERC1	GRCh38.p7	15:63695404	TTTTTTTTTTTTTTT[G/T]AGATGGAGTCTTGCT	8925
rs76668598	snp	C/T	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63711499	AGGAGGAAGTATAAA[C/T]AAAATGTCATGATAC	8925
rs76744224	snp	C/T	0.0260207	0.111123	intron-variant	HERC1	GRCh38.p7	15:63726430	AATGGATAAGTTATC[C/T]AAAAGGAAAATGGAT	8925
rs76813158	snp	C/T	0.02016	0.0983543	intron-variant	HERC1	GRCh38.p7	15:63831571	ACGATGTCATCATTA[C/T]CATCATTTTAAGATC	8925
rs76836538	snp	C/T	0.171704	0.237423	intron-variant	HERC1	GRCh38.p7	15:63746412	CCCCCAAATTTAACA[C/T]TGTATTATAATACTA	8925
rs76864518	snp	A/T	0.0460142	0.144533	intron-variant	HERC1	GRCh38.p7	15:63659020	TCACATCTACTGATT[A/T]TAAGTGCTTTGAGAA	8925
rs76892063	snp	G/T	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63672232	TATCATCATAAGAGA[G/T]AGAATGTTAGACTAC	8925
rs76927788	snp	A/G	0.0252325	0.109451	intron-variant	HERC1	GRCh38.p7	15:63722104	TCCTGACCTCAAGTG[A/G]TACCTCCCACCTCAG	8925
rs76946928	snp	A/C/T	0.0107246	0.0724382	intron-variant	HERC1	GRCh38.p7	15:63680301	ATTAACCTTGCTAAC[A/C/T]GAGAAAATTCTACAT	8925
rs76965353	snp	C/T	0.0532157	0.154195	intron-variant	HERC1	GRCh38.p7	15:63814282	TTACAACAAATATAT[C/T]ACTTTTCACACTTAG	8925
rs76985055	snp	A/T	0.375	0.216506	intron-variant	HERC1	GRCh38.p7	15:63647655	GTGGCTGAATAGAAT[A/T]CTATCAGGTATATAT	8925
rs77005371	snp	C/G	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63613189	CTCTCTTAATTTTTC[C/G]GTCTGAAAAAAGCAG	8925
rs77010591	snp	A/G/T	0.0213413	0.101131	intron-variant	HERC1	GRCh38.p7	15:63629605	ATTAGGAAGGATCAC[A/G/T]TCACGGCACTGCCAG	8925
rs77066856	snp	C/G	0.0659589	0.169201	intron-variant	HERC1	GRCh38.p7	15:63776425	TTGTAGAATGGAACA[C/G]CCACTTTGGAAAGGT	8925
rs77075313	snp	A/G	0.040671	0.13668	intron-variant	HERC1	GRCh38.p7	15:63609577	GCCTGGCACAGGATG[A/G]GAGTGTAGTAAGAGG	8925
rs77080166	snp	A/C	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63723546	ACATTCTCCAAAAGG[A/C]TGTGACACTCTACCA	8925
rs77087691	snp	C/G	0.0118607	0.07609	utr-variant-3-prime, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609057	TATTGAGGGAGAGAA[C/G]GGAGGGTGAGAGCAC	8925
rs77099700	snp	C/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63644510	CTTTGTTTTTTTTTT[C/T]TGTTTTTGCTTTTTA	8925
rs77106746	snp	C/G	0.040671	0.13668	intron-variant	HERC1	GRCh38.p7	15:63718289	ATGTGGCCCAATCAG[C/G]ACAAAGAGAGGAATA	8925
rs77106865	snp	G/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63741026	TTTACATCTATGTTG[G/T]TTTTTTTTTTATTTT	8925
rs77107306	snp	A/G	0.175897	0.238765	intron-variant	HERC1	GRCh38.p7	15:63681502	ACACCTAGTGTGACT[A/G]TTACTATTTTCAAAA	8925
rs77148449	snp	C/T	0.067446	0.170804	intron-variant	HERC1	GRCh38.p7	15:63763230	AATAAAAAGAAACGA[C/T]AGAATTAGAATATCA	8925
rs77151950	snp	A/G	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63828358	CCTTTTTTTTTTTTA[A/G]GACAAAGTTTTGCTC	8925
rs77169245	snp	A/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63730309	AAATTTTTTTTTTTA[A/T]TTAGCTGAGCATGGT	8925
rs77248963	snp	A/C	0.0345262	0.126772	intron-variant	HERC1	GRCh38.p7	15:63652313	CTAAAAGAAAATTTC[A/C]AAAAATTTTAGTGAC	8925
rs77258879	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63825170	AAAAATTAGCCAGGT[A/G]TGGCAGCACACACCC	8925
rs77328052	snp	C/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63827094	AGATGAATGGTTGAA[C/G]AGGTTAAGAAACATC	8925
rs77339802	snp	A/G	0.0231532	0.105074	intron-variant	HERC1	GRCh38.p7	15:63734866	TAATATCAAAAGAGA[A/G]AAGTATACTGATTGG	8925
rs77340786	snp	C/T	0.0626037	0.165477	intron-variant	HERC1	GRCh38.p7	15:63667765	TCTAAAAATATAAAA[C/T]GAAGTACAGTTGACT	8925
rs77357604	snp	C/T	0.0663309	0.169604	intron-variant	HERC1	GRCh38.p7	15:63831092	AAGTTGTGTAGACCT[C/T]TGTTGTTGTTTGTTT	8925
rs77380928	in-del	-/TTA			intron-variant	HERC1	GRCh38.p7	15:63701040	GGGGGGTGTTTTTTT[-/TTA]AATATTAAAATTTTA	8925
rs77438195	snp	C/T	0.0154538	0.0865337	intron-variant	HERC1	GRCh38.p7	15:63829013	AGTATACTTACTCTA[C/T]ATCATGAAAGCCAGG	8925
rs77455514	snp	A/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63829264	TCTCTACTAAAAATT[A/T]AAAAAAAATCAGCGG	8925
rs77516070	snp	A/C			missense	HERC1	GRCh38.p7	15:63775517	AGTTTAGAATACAGA[A/C]CAGCAACTCCCTCTC	8925
rs77517168	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63740055	ATCTGGGACTACAGG[A/C]ATGCGCCACCAGACT	8925
rs77568702	snp	A/G	0.0984431	0.198823	intron-variant	HERC1	GRCh38.p7	15:63804304	TCAAAAAGTATTGCT[A/G]GCCGGGCACAGTGGC	8925
rs77573824	snp	A/C	0.0659589	0.169201	intron-variant	HERC1	GRCh38.p7	15:63799557	CTTTCTGCCAGTATC[A/C]AAAGGAGGCAATGAT	8925
rs77575316	snp	A/T	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63816601	TCATGATGAGATTTT[A/T]ACCTATTTATTTACC	8925
rs77612960	in-del	-/AAAG			intron-variant	HERC1	GRCh38.p7	15:63730045	AAAAAAAAAAAAAAA[-/AAAG]CATTATATCCTTTCT	8925
rs77615461	snp	A/G	0.0414363	0.137845	intron-variant	HERC1	GRCh38.p7	15:63744956	GCCCATGGGCTCTTC[A/G]GTTAGCAGGTGATGA	8925
rs77619883	snp	G/T	0.0659589	0.169201	intron-variant	HERC1	GRCh38.p7	15:63797512	TCATCACACCAGGAC[G/T]GTTTTTCACACTCCA	8925
rs77620446	snp	C/T	0.00636936	0.0560724	intron-variant	HERC1	GRCh38.p7	15:63811414	CTAGGTGAAAAGCGC[C/T]ATTCTTCATTTTTTC	8925
rs77715851	snp	C/G	0.263535	0.249633	intron-variant	HERC1	GRCh38.p7	15:63649082	CATCTCGGCCAGGCA[C/G]GGTGGCTCACGCCTG	8925
rs77735327	snp	A/T	0.0244538	0.107838	intron-variant	HERC1	GRCh38.p7	15:63682615	CATCTCTACAAAATA[A/T]ACAAAAACAAACAAA	8925
rs77811935	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63788536	ATAAAGTAACAATAG[A/C]AAAACTTAATGAAGC	8925
rs77812916	snp	C/T	0.0150606	0.0854603	intron-variant	HERC1	GRCh38.p7	15:63826324	GTTTAATTTTCATTA[C/T]GACTGCCCTTCTTCC	8925
rs77832846	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63799197	GTTCTGATACTTAAG[A/G]CTTTAACAAAAAGTA	8925
rs77840866	snp	A/C	0.329783	0.236927	intron-variant	HERC1	GRCh38.p7	15:63732108	CTGGTTCAAGCAACT[A/C]TCCCACCTCGGCCTC	8925
rs77844337	snp	A/G	0.0372196	0.131242	intron-variant	HERC1	GRCh38.p7	15:63705205	GTCACACAGGCTGGA[A/G]TGCAGTGGCATGATC	8925
rs77885398	snp	A/G	0.00914312	0.0669923	intron-variant	HERC1	GRCh38.p7	15:63630774	GAGGCTAAAGCTGCT[A/G]TTCTGGAAAGGTACA	8925
rs77891017	snp	A/G	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63712354	TAACTGGATTGGGAA[A/G]GGGTGGAGAATAAAG	8925
rs77891602	snp	A/T	0.02016	0.0983543	intron-variant	HERC1	GRCh38.p7	15:63684523	TGGACAAAAAGGTCT[A/T]GATAAAAATAACAAA	8925
rs77896373	snp	A/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63681604	AAAAAAAAAAAAACT[A/T]CCCCTACGTGATAAA	8925
rs77964412	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63819772	AACTATGTCATTGAG[C/G]CTGGCCATGTCTATG	8925
rs77972385	in-del	-/TTT			intron-variant	HERC1	GRCh38.p7	15:63706726	TGCTCTTTTTTTTTT[-/TTT]GAGACAGGGTCTCAC	8925
rs77974507	snp	G/T	0.0652144	0.168387	intron-variant	HERC1	GRCh38.p7	15:63794286	CTCGCCCTGAATTCT[G/T]TCTTGCGTGAGATCC	8925
rs77989708	snp	C/G	0.0517044	0.152246	intron-variant	HERC1	GRCh38.p7	15:63719569	ATTTTTGAAAGCTCA[C/G]TCTGCTGAGTGGAGA	8925
rs78016693	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63808994	CATTCTTATGGCCTC[C/G]CTAAAATAAAAAATG	8925
rs78043072	snp	C/T	0.0399052	0.1355	intron-variant	HERC1	GRCh38.p7	15:63704276	TTCACATTCAAATTA[C/T]AGTTTTTTCTTAGTT	8925
rs78044194	snp	A/C	0.0205511	0.0992634	intron-variant	HERC1	GRCh38.p7	15:63832319	CGTACATTTATGCAT[A/C]AGACAGGCACCTAGG	8925
rs78063098	snp	A/C/T	0.250865	0.249999	intron-variant	HERC1	GRCh38.p7	15:63660333	TCAAAGAAATAAAAA[A/C/T]AATAAATAAATAAAT	8925
rs78063383	snp	C/T	0.00716266	0.059414	intron-variant	HERC1	GRCh38.p7	15:63641333	TTTAGGCATGACTTA[C/T]CTTCATTTGATTCTG	8925
rs78079961	snp	A/G	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63624773	AACTCAGGATTAGGA[A/G]CTATTAGTAACCTTT	8925
rs78084910	snp	A/G	0.00519162	0.0506839	intron-variant	HERC1	GRCh38.p7	15:63734869	TATCAAAAGAGAAAA[A/G]TATACTGATTGGCCT	8925
rs78088275	snp	G/T	0.0652144	0.168387	intron-variant	HERC1	GRCh38.p7	15:63786686	TCTATTTATAAGAAA[G/T]GTACAGTACAGGATG	8925
rs78111261	snp	A/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63821748	AAAAAAAAAAAAAAA[A/T]AATCAGATAATCTAA	8925
rs78158636	snp	C/T	0.0603597	0.1629	intron-variant	HERC1	GRCh38.p7	15:63827784	TGTAGTATATTCACA[C/T]AACGGAATAACATTC	8925
rs78188233	snp	C/T	0.0659589	0.169201	intron-variant	HERC1	GRCh38.p7	15:63818767	AACATTTCACTACTG[C/T]CACATATCTGCCTTT	8925
rs78272672	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63635866	TTACTGTGTAATATA[C/T]TTTTACTATATTTTC	8925
rs78276338	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63633719	CAAGAATGCACAACA[A/G]AAGCTTCTAAACTTC	8925
rs78277310	snp	C/G	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63659605	ACAACTGGCTAAAGA[C/G]ACTTGTTGGGGTGAG	8925
rs78277541	snp	A/T	0.0704125	0.17392	intron-variant	HERC1	GRCh38.p7	15:63614471	GGAGACAAACACTAA[A/T]CCCTGGCTGTGTAAA	8925
rs78279488	in-del	-/GA			intron-variant	HERC1	GRCh38.p7	15:63760454	AAAAAAAAAAAAAAA[-/GA]AGACACAAAGGAAAA	8925
rs78285098	snp	A/T	0.02016	0.0983543	intron-variant	HERC1	GRCh38.p7	15:63790806	TTAATTCTCTGTACT[A/T]CTCTTCAGTCTTAAA	8925
rs78323570	snp	A/G	0.0704125	0.17392	intron-variant	HERC1	GRCh38.p7	15:63634090	TTCCAAATATCTACA[A/G]TGGTTTCAGAGCATA	8925
rs78336653	snp	A/G	0.040671	0.13668	intron-variant	HERC1	GRCh38.p7	15:63656940	TCATTTATCCCTACA[A/G]ATGACAATCAGGCGG	8925
rs78339751	snp	A/G	0.0368353	0.130617	intron-variant	HERC1	GRCh38.p7	15:63656615	ACAGGAATGTTCACA[A/G]AGCATAAATTTTCAT	8925
rs78341289	snp	A/G	0.0279145	0.114796	intron-variant	HERC1	GRCh38.p7	15:63643073	CCTAAAATGAGATAT[A/G]TTTACCAATACACAC	8925
rs78381038	snp	A/G	0.5	0	missense	HERC1	GRCh38.p7	15:63734842	ACTGATAAAGTTTCA[A/G]TTACCACCTAATATC	8925
rs78411394	snp	A/G	0.375	0.216506	intron-variant	HERC1	GRCh38.p7	15:63647396	ATTTACATTCCCACC[A/G]ACAGGGTGTAAGAGT	8925
rs78427109	snp	A/G	0	0	intron-variant	HERC1	GRCh38.p7	15:63760453	AAAAAAAAAAAAAAA[A/G]AAGACACAAAGGAAA	8925
rs78464419	snp	G/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63683223	CTAAAGTTTCATCCT[G/T]ATCAGGGAAAGCTCC	8925
rs78471468	snp	A/G	0.0663309	0.169604	intron-variant	HERC1	GRCh38.p7	15:63813543	AAAAACAATAAAATG[A/G]AGATTTACACTACTC	8925
rs78488326	snp	C/T	0.00795532	0.062565	intron-variant	HERC1	GRCh38.p7	15:63667946	CTTCCACTTAATGAA[C/T]AGTAAATATATCTTC	8925
rs78501075	snp	A/T	0.32955	0.237006	intron-variant	HERC1	GRCh38.p7	15:63732107	CCTGGTTCAAGCAAC[A/T]CTCCCACCTCGGCCT	8925
rs78501477	snp	A/G	0.0252325	0.109451	intron-variant	HERC1	GRCh38.p7	15:63823958	ACGCAATAGCAAAAA[A/G]CAAAAATGAATAACC	8925
rs78512963	snp	A/G	0.0345262	0.126772	intron-variant	HERC1	GRCh38.p7	15:63722428	AATAGATCCATTTAC[A/G]TAGCACGGAATATAA	8925
rs78515517	snp	C/G	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63820046	TATGTAAATTAGCTA[C/G]ATTTAGTCATTCCAC	8925
rs78517126	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63738996	ATTTTTTTTTTTTCA[A/T]ATTGACATATAATCC	8925
rs78520774	snp	C/T	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63683890	TCTAATTGCCTGGAC[C/T]TGACTATAAGCTAAA	8925
rs78590919	snp	A/T	0.0209421	0.100162	intron-variant	HERC1	GRCh38.p7	15:63665157	TCACAGCAATCTTTT[A/T]ACACTTAAAGGGGCA	8925
rs78594811	snp	C/G	0.0193772	0.0965046	intron-variant	HERC1	GRCh38.p7	15:63691571	ACTGTAATAAGATCA[C/G]TTGAAAATAAATGAA	8925
rs78614236	snp	C/T	0.0360663	0.129354	intron-variant	HERC1	GRCh38.p7	15:63737493	CCAGATATATATATA[C/T]ACATATATATATCTT	8925
rs78615739	snp	A/G	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63824843	CACAAGTCAGACGTA[A/G]GAAAAAAAAAAAACA	8925
rs78649500	snp	C/T	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63793959	GACCTTCTAATAAAA[C/T]AGGTTACAGTAAAGG	8925
rs78655579	snp	C/T	0.02016	0.0983543	intron-variant	HERC1	GRCh38.p7	15:63805674	ACAAAAGGTCAGACA[C/T]TATGGCTGAGGCCTA	8925
rs78656140	snp	A/G	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63748251	TATATACATATATAC[A/G]TTAAAGCTGAATGAG	8925
rs78656274	snp	A/G	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63613201	TTCCGTCTGAAAAAA[A/G]CAGATATTGCTGCTC	8925
rs78657326	snp	C/G	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63649639	AGATAATATTCACTT[C/G]GTATTTTTAAAAGCA	8925
rs78663880	snp	C/G	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63801951	CCCACTCAGATGTAC[C/G]AAAGGAATCTCTAAC	8925
rs78685408	snp	C/T	0.02016	0.0983543	intron-variant	HERC1	GRCh38.p7	15:63765056	CTGACGGCTGACTTA[C/T]GCAAGAAGCTGCCTT	8925
rs78686299	snp	C/T	0.0341408	0.126114	intron-variant	HERC1	GRCh38.p7	15:63750931	AAAAGAGTGAGACCC[C/T]GAGTTCAAAATAAAA	8925
rs78687715	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63662590	GAATAAGGCATTACA[C/T]TGATTAAATGGAACC	8925
rs78732015	snp	G/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63825782	AATTTTTTTTTTTTT[G/T]AGATGGAGTCTCGTT	8925
rs78738976	snp	A/G	0.0115144	0.0749975	intron-variant	HERC1	GRCh38.p7	15:63706575	CCAGATTTTTAAAGC[A/G]TACATATTTTAAAGA	8925
rs78747363	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63632437	CAGCATGTCAAGGGC[A/G]GTAGAAAAGAAGAGG	8925
rs78796463	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63801005	TCAACCAAGCCTACG[C/T]AATGCAGCTTCCATA	8925
rs78806317	snp	C/T	0.0248432	0.108648	intron-variant	HERC1	GRCh38.p7	15:63703391	CATGGAAAGAGCAGC[C/T]GAAAATGTGTATACA	8925
rs78822375	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63808992	CTCATTCTTATGGCC[G/T]CCCTAAAATAAAAAA	8925
rs78824147	snp	C/T	0.0298908	0.118541	intron-variant	HERC1	GRCh38.p7	15:63616129	TGGGACAAAATCTCT[C/T]TGTTCACAAACCAAG	8925
rs78835439	snp	A/C	0.0375992	0.131856	intron-variant	HERC1	GRCh38.p7	15:63718543	CACAGCTTGCAGAAA[A/C]ACATAGAAATTAATT	8925
rs78837403	snp	A/G	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63785198	AAGAGGCCAAGGTGG[A/G]AGGAAGCTTTAGGCC	8925
rs78857043	snp	A/C	0.179105	0.239737	intron-variant	HERC1	GRCh38.p7	15:63668667	GATTTCAGGGCAAAA[A/C]AATATCACCAAGGAT	8925
rs78896533	snp	C/T	0.0193772	0.0965046	intron-variant	HERC1	GRCh38.p7	15:63795259	CTAAAGCTTGCCTTT[C/T]TCAATGGTTTTATTA	8925
rs78907238	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63700773	AAAAATAACAACCTA[C/T]CTAAAAATTTCCCCA	8925
rs78922900	snp	C/G	0.0505692	0.150756	intron-variant	HERC1	GRCh38.p7	15:63787518	CCCAAAATGAACTGA[C/G]GGTATGTTACTGAAA	8925
rs78962982	snp	A/G	0.0138799	0.0821421	intron-variant	HERC1	GRCh38.p7	15:63638097	TGGCTAAAGATCCTA[A/G]GAAGTTTTTAGCCCC	8925
rs78972249	snp	C/T	0.02016	0.0983543	intron-variant	HERC1	GRCh38.p7	15:63773123	ATTTGTTGGTTGACA[C/T]CTGGTAACAAAGGAT	8925
rs78998206	snp	A/G	0.00294365	0.0382513	synonymous-codon	HERC1	GRCh38.p7	15:63733098	AAGTAGGGAGGCTAC[A/G]TGGGTATGATCTTGC	8925
rs79022805	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63747915	GAAATTTTTATGCAC[A/G]ATCAAAAACGAAAAT	8925
rs79062716	snp	A/G	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63610147	TAAAAAAAAAAAAAA[A/G]AACCTGTCTTCTCTC	8925
rs79088625	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63720000	GTACATTTAAGTGGG[C/T]AAGAAATGAAACAAC	8925
rs79092379	snp	C/T	0.0197687	0.0974348	intron-variant	HERC1	GRCh38.p7	15:63665686	TTCAGTACAATTTTA[C/T]ACAAAAATTATGAAA	8925
rs79094360	snp	C/T	0.02016	0.0983543	intron-variant	HERC1	GRCh38.p7	15:63691879	GCAAATTTCACGTTA[C/T]GTGCATTTTACCACA	8925
rs79123077	in-del	-/TT			intron-variant	HERC1	GRCh38.p7	15:63738992	GTTTATTTTTTTTTT[-/TT]CAAATTGACATATAA	8925
rs79157803	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63637779	AAAGGGAAGAGTTGA[A/T]ATAACTATGCAGTCC	8925
rs79176409	snp	A/C	0.0335676	0.125128	missense	HERC1	GRCh38.p7	15:63725445	TTCTTTCTAGATCCA[A/C]AAGCCATACCCAGGA	8925
rs79184094	snp	C/T	0.00914312	0.0669923	intron-variant	HERC1	GRCh38.p7	15:63742947	CTATAGTTTTTCTTT[C/T]CTTGCAATGTTTTGG	8925
rs79228948	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63822754	AGACTATTATAATTA[A/C]CCACACAGGAGATGG	8925
rs79246166	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63773463	AAAAAAAAAAAAAAA[A/G]ACTTGATCAATGTAA	8925
rs79267723	snp	A/G	0.0287284	0.116357	intron-variant	HERC1	GRCh38.p7	15:63676483	TTGTTCCGGCCGAGC[A/G]TGGTGGCTCATGTCT	8925
rs79279857	snp	A/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63828356	TTCCTTTTTTTTTTT[A/T]AAGACAAAGTTTTGC	8925
rs79292693	snp	C/T	0.0663309	0.169604	intron-variant	HERC1	GRCh38.p7	15:63830287	CCCCAATATGATGCA[C/T]TGAGAAGGACACAAC	8925
rs79374032	snp	C/G	0.330249	0.23677	intron-variant	HERC1	GRCh38.p7	15:63739072	TTTAGTCTATTCAGA[C/G]TTGTGCAACCATCAC	8925
rs79375822	snp	A/T	0.0197687	0.0974348	intron-variant	HERC1	GRCh38.p7	15:63667418	ACGGAAGATGAGATT[A/T]AAAAAAAACAAATCA	8925
rs79410476	snp	C/T	0.100588	0.200439	intron-variant	HERC1	GRCh38.p7	15:63767145	TAGCTGGATTACAAG[C/T]GCACGCCACCATGCT	8925
rs79418206	snp	G/T	0.0391387	0.134304	intron-variant	HERC1	GRCh38.p7	15:63610406	CGACCACGGTAGTCA[G/T]TTACTGATGCTGACA	8925
rs79421212	snp	A/G	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63663771	ATGTTAATCATATAG[A/G]AAAAAACTTCAATAA	8925
rs79452983	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63812520	GATTCAAAAGGAAAT[A/G]GGAAGTTTCTCCTGT	8925
rs79472798	snp	C/T	0.0193772	0.0965046	intron-variant	HERC1	GRCh38.p7	15:63655472	AAACAAAGAGAAAAA[C/T]AACACTGCCTTCATC	8925
rs79477466	snp	A/G	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63613200	TTTCCGTCTGAAAAA[A/G]GCAGATATTGCTGCT	8925
rs79490559	snp	A/T	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63763874	AAGTTACCAGCACAT[A/T]ATTCAAAAATCAAAA	8925
rs79503123	snp	C/T	0.0490535	0.14873	intron-variant	HERC1	GRCh38.p7	15:63719606	TTATAGGGACAGCAA[C/T]AGCAGAAGTAATTAT	8925
rs79538392	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63709798	TAGATTTCTAGTGGG[C/T]TTACTGGGAAGACAT	8925
rs79549965	snp	G/T	7.25058e-05	0.0060206	missense	HERC1	GRCh38.p7	15:63656187	GCAAGAGATAGGCTT[G/T]TTAGCCTTGCTATGC	8925
rs79552571	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63688364	ACGTGATTAAGGGTG[A/C]CATTTTTGACATACT	8925
rs79554011	snp	A/C	0	0	intron-variant	HERC1	GRCh38.p7	15:63809793	GTTTAGAATAGCAAA[A/C]AAAAAAAAAAAAGTA	8925
rs79559105	snp	C/T	0.00546685	0.0519956	intron-variant	HERC1	GRCh38.p7	15:63746900	TGAGATACAGATTCA[C/T]AAGTCCTATTCTCTT	8925
rs79620829	snp	A/G	0	0	intron-variant	HERC1	GRCh38.p7	15:63610146	TTAAAAAAAAAAAAA[A/G]GAACCTGTCTTCTCT	8925
rs79644651	snp	A/G	0.0693013	0.172766	intron-variant	HERC1	GRCh38.p7	15:63786687	CTATTTATAAGAAAT[A/G]TACAGTACAGGATGG	8925
rs79685102	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63787985	AAAAAAAAAAAAAGA[A/C]AAAACAAAACAAAAA	8925
rs79686310	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63639814	TCTATATGTGGCATA[C/T]AACCCACAAGATGAC	8925
rs79704534	snp	G/T	0.0287284	0.116357	intron-variant	HERC1	GRCh38.p7	15:63663532	ACAATCCCAGCTCAC[G/T]GTAACCCTGAACCCC	8925
rs79711865	snp	C/T	0.000283373	0.0118999	missense	HERC1	GRCh38.p7	15:63665932	ACCTTTCACTAAAAC[C/T]TTCCTCCATTTCAGC	8925
rs79714693	snp	C/T	0.178465	0.239547	intron-variant	HERC1	GRCh38.p7	15:63701264	TTTATGGGAGGTAGT[C/T]TTACATATTCATTAT	8925
rs79718858	snp	C/G	0.040671	0.13668	intron-variant	HERC1	GRCh38.p7	15:63760244	ACAAAAAAAAACAGA[C/G]GGAGGGAGTCTATGG	8925
rs79731249	snp	C/T	0.0283406	0.115616	intron-variant	HERC1	GRCh38.p7	15:63818370	TACAAAAACCCTTTC[C/T]TGCCTGCCTACTCTG	8925
rs79732157	snp	C/T	0.0402882	0.136092	intron-variant	HERC1	GRCh38.p7	15:63800975	AGAGTTAATCACCAA[C/T]GGTCAACGATTTAAT	8925
rs79787166	snp	A/G	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63647491	CAATCCAGCGATACC[A/G]CTGCTAGGTATCTAT	8925
rs79790626	snp	A/T	0.0356815	0.128715	intron-variant	HERC1	GRCh38.p7	15:63748241	AAAAAATATATATAT[A/T]CATATATACATTAAA	8925
rs79790777	snp	C/T	0.00597247	0.0543191	intron-variant	HERC1	GRCh38.p7	15:63814905	AGTATTTTAATGCAA[C/T]GTACTAATGTGAGCT	8925
rs79826128	snp	C/T	0.0158469	0.0875917	intron-variant	HERC1	GRCh38.p7	15:63781006	AGTGATTTCAAAATG[C/T]TGAAGATAAAATGTA	8925
rs79849161	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63641273	TCTTTATTTTACTCT[A/G]GTGAAAATAAAGCAA	8925
rs79881652	snp	C/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63770291	TTCCTCCGTAAGACA[C/T]TTTCGGTCCCTTTGC	8925
rs79883717	snp	A/C	0.0154538	0.0865337	intron-variant	HERC1	GRCh38.p7	15:63810893	AGGAGTACATAACAT[A/C]ACCTACATAGTGTTA	8925
rs79890462	snp	C/T	0.00676609	0.0577691	intron-variant	HERC1	GRCh38.p7	15:63807436	CTAGCTTGGCTTCCA[C/T]TGCTCCAGCTCTCAT	8925
rs79907206	snp	A/G	0.0648419	0.167978	intron-variant	HERC1	GRCh38.p7	15:63732438	CATTATTAGCACTGA[A/G]TCATAATGATCTGGC	8925
rs79908474	snp	C/T	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63785961	TCTTCCCACTTGGGC[C/T]TCCCAAAGTGCTGGG	8925
rs79919472	snp	C/T	0.0126165	0.0784161	intron-variant	HERC1	GRCh38.p7	15:63747893	AATAATAAAACAGTC[C/T]TAAAATGAAATTTTT	8925
rs79957244	snp	C/G	0.0138799	0.0821421	intron-variant	HERC1	GRCh38.p7	15:63832612	TATACATAGGTACTA[C/G]ACCCAAACAGACAAT	8925
rs79976004	snp	A/T	0.201727	0.245295	intron-variant	HERC1	GRCh38.p7	15:63695384	TGAGTCTGTATAATC[A/T]TTTTTTTTTTTTTTT	8925
rs79986168	snp	A/G	0.0581099	0.160244	intron-variant	HERC1	GRCh38.p7	15:63785008	GACAAAGAGAGGAAG[A/G]GGAAAGGAGTTACAA	8925
rs79992938	snp	G/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63828359	CTTTTTTTTTTTTAA[G/T]ACAAAGTTTTGCTCT	8925
rs80008300	in-del	-/AAAA			intron-variant	HERC1	GRCh38.p7	15:63696948	TAAAAAAAAAAAAAA[-/AAAA]TTATTTTGAAATAAT	8925
rs80024345	snp	G/T	0.00437853	0.0465843	intron-variant	HERC1	GRCh38.p7	15:63645463	AAACTAAGACGTATA[G/T]ATGCAAATTGACAAC	8925
rs80029078	snp	A/C	0.0547245	0.156101	intron-variant	HERC1	GRCh38.p7	15:63740265	TGTATCACTACTTCA[A/C]TCCTTTTTATGGCTA	8925
rs80032429	snp	A/C	0.0064007	0.0562084	missense	HERC1	GRCh38.p7	15:63658650	GGTCATGAGGGTTTG[A/C]TAGGGCAGCTGCCTG	8925
rs80047978	snp	A/G	0.169435	0.236663	intron-variant	HERC1	GRCh38.p7	15:63806495	TTTGTTATTATTTGC[A/G]TACCTGTCTTCATCA	8925
rs80054172	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63798283	AATCTGATGTTACTC[C/T]CTTAGTGAAAACCCC	8925
rs80054863	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63832157	TTGTCATGTGATTTG[A/G]GGGAAATATTATGAC	8925
rs80056088	snp	C/T	0.0138799	0.0821421	intron-variant	HERC1	GRCh38.p7	15:63815507	ATGTAGTAAATGTTA[C/T]ATAGTGACTGATGAA	8925
rs80084213	snp	G/T	0.0501905	0.150254	intron-variant	HERC1	GRCh38.p7	15:63810117	AAATGATTACTATGA[G/T]ATACTAAGTTAAAAA	8925
rs80088271	snp	A/G	0.0663309	0.169604	intron-variant	HERC1	GRCh38.p7	15:63638599	ACAGCCATGTACTAC[A/G]TACCAAGTGTGTGCC	8925
rs80096136	snp	C/T	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63666731	ATCCAAGTTCCATAT[C/T]TGTAAATCTGTATAC	8925
rs80145154	snp	C/T	0.00835141	0.0640778	intron-variant	HERC1	GRCh38.p7	15:63615124	CAACTAGAGTGGAGA[C/T]GCTGAGCTGGGAAGC	8925
rs80156324	snp	A/G	0.0182019	0.0936463	intron-variant	HERC1	GRCh38.p7	15:63614698	TGAAATGCTATTAAT[A/G]ACTGTATTATCAAAA	8925
rs80181687	snp	G/T	0.095934	0.196885	intron-variant	HERC1	GRCh38.p7	15:63784987	TTTTGGAAACTAAGT[G/T]TCTCAGACAAAGAGA	8925
rs80201845	snp	A/G	0.000563231	0.0167719	synonymous-codon	HERC1	GRCh38.p7	15:63661779	TGTTGACTTAGATTT[A/G]GTCTTCATGGCTAAG	8925
rs80203202	snp	C/T	0.00419902	0.0456276	missense	HERC1	GRCh38.p7	15:63725486	TGAGGTAATGGCAGA[C/T]CAGCAGGATCAATTA	8925
rs80204188	snp	A/C	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63768511	GTTGCAACCTCTCCA[A/C]ATTCCCTAGTTAGCT	8925
rs80205347	snp	A/G	0.0475351	0.146656	intron-variant	HERC1	GRCh38.p7	15:63792706	TGACCAAATGTGTGG[A/G]AGATTTTCTCCACAC	8925
rs80235525	snp	A/T	0.0399052	0.1355	intron-variant	HERC1	GRCh38.p7	15:63782344	ACATTCTGAAAAACC[A/T]AGGGCACCTAAGAAT	8925
rs80248301	snp	C/T	0.0154538	0.0865337	intron-variant	HERC1	GRCh38.p7	15:63816358	GCTGCTCCAGTTCTT[C/T]GACAGCTTTTAATAA	8925
rs80251214	snp	C/T	0.151334	0.229706	intron-variant	HERC1	GRCh38.p7	15:63655119	AGGACTTTGGGAGGT[C/T]GAGGTGGGAGGATCA	8925
rs80265381	snp	C/T	0.0663309	0.169604	intron-variant	HERC1	GRCh38.p7	15:63709733	CAATATGTAAAGCAC[C/T]GTGTAGGAGATATCA	8925
rs111265744	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63618961	GACAATTTGACTTCC[C/T]CTTTTCCTAACTGAA	8925
rs111410388	snp	C/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63684704	TTCTCTACCTTCTAG[C/T]GGGGGAAAAAAATCT	8925
rs111531959	in-del	-/A	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63757130	TTCTAAACCTATTTG[-/A]AAAAAAAAATACATT	8925
rs111577041	in-del	-/A	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63674315	CAACAGCACAAAAGC[-/A]AAAAAAAAAAAAATC	8925
rs111597565	snp	A/G	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63752299	CCTATACATGACAGA[A/G]TAAGTGGCCAGCTCA	8925
rs111605289	snp	A/G	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63705477	ATTTTAAGTAACAAC[A/G]TTTATTCTTTTGAGC	8925
rs111607865	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63805937	AACAGAGCAAGACCC[C/T]ATCTCAAAACAAAAA	8925
rs111632626	snp	A/G	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63793848	TAGGAGCTGGGTAAA[A/G]TGAGGCTGAGACCTA	8925
rs111699325	snp	A/G	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63623579	CTAATTTACCTACGT[A/G]TCACTAACAGCATCA	8925
rs111722218	snp	C/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63674095	TTTTGTTTTACAAAA[C/T]GTAGTAATAATTGCT	8925
rs111747044	snp	A/G	0.0205511	0.0992634	intron-variant	HERC1	GRCh38.p7	15:63691237	TTGGGAGGCTGAGGC[A/G]GGCAGATCACTTAAG	8925
rs111747714	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63737547	TATATATATATATAT[A/C]TCTTTTTTTTTTTTA	8925
rs111762379	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63833713	TCCCGAAACGGCCCC[C/G]GCCGGCCCTGCGCGG	8925
rs111764186	snp	C/T	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63793702	CCCTGAATTCTTTCT[C/T]GCGCAAGATCCAAGA	8925
rs111776050	snp	A/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63820193	TGTTCAGTGTGCTAG[A/T]GTTATTCCTTTATAT	8925
rs111834387	snp	C/G	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63770012	TTTCCTTCCGTTCTG[C/G]CTGTTTTTACTCAAA	8925
rs111850058	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63620545	TTCAATTCCTGGATA[C/T]CCTTGTTAACTTTCT	8925
rs111873527	snp	A/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63709167	AATATATATATATAT[A/T]TTTTATTTTTTTGTA	8925
rs111884935	in-del	-/A	0.310878	0.242475	intron-variant	HERC1	GRCh38.p7	15:63711315	GTAATATCCTGTCTC[-/A]AAAAAAAAGGGAAAT	8925
rs111918936	snp	A/G	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63654651	TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA	8925
rs111972512	snp	A/G	0.0655868	0.168795	intron-variant	HERC1	GRCh38.p7	15:63747188	TTGTTGGCTAGGTGC[A/G]GTGGCTCATGCCTGT	8925
rs112009411	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63802158	GGTCCAGGTCTCCCC[A/T]CTCCTGCCACATGTA	8925
rs112027308	snp	C/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63657856	TATGTGGATAAACCA[C/T]CAGACCCTGCTTCAG	8925
rs112090180	snp	A/G	0.00597247	0.0543191	intron-variant	HERC1	GRCh38.p7	15:63816936	TACATATCTCCCGAT[A/G]GAAACAAAAATCACT	8925
rs112109480	snp	C/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63673678	ATGAAAGTAGAGACT[C/T]TAAAATTTATTTTAA	8925
rs112134914	snp	C/G	0.0707826	0.174302	intron-variant	HERC1	GRCh38.p7	15:63793709	TTCTTTCTTGCGCAA[C/G]ATCCAAGAACCCTCT	8925
rs112158787	snp	C/T	0.00676609	0.0577691	intron-variant	HERC1	GRCh38.p7	15:63807314	ATTGAGAGGCACACA[C/T]AGGAGGAAATGGGAG	8925
rs112174350	snp	C/T	0.0197687	0.0974348	intron-variant	HERC1	GRCh38.p7	15:63671198	ACAAGAGTGAAACTT[C/T]GTCTCAAAAAAAAAA	8925
rs112226526	in-del	-/GCTTTAGTA	0.361894	0.223562	intron-variant	HERC1	GRCh38.p7	15:63743986	ATCTAAACTGTATCT[-/GCTTTAGTA]ACGTTGTGGTTCTTG	8925
rs112305294	snp	A/G	0.16976	0.236773	intron-variant	HERC1	GRCh38.p7	15:63789557	GATCCCCGCACTTCG[A/G]AAAGCCGAGGCAGGC	8925
rs112377991	snp	C/T	0.0123036	0.0774623	intron-variant	HERC1	GRCh38.p7	15:63687086	TGTGTGTCATATTGT[C/T]TGAATTTTACTCTAC	8925
rs112382815	snp	A/G	6.91934e-05	0.00588149	intron-variant	HERC1	GRCh38.p7	15:63612565	CAGCCACCTGCTCCC[A/G]GGAGAGGTTGCTCAT	8925
rs112390971	snp	C/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63708319	AATTATGTAACTCAT[C/T]ATGCTTTTCCTGTGT	8925
rs112409282	snp	A/G	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63777985	AACACCATTTATTAA[A/G]TAATCCAGGACTTCT	8925
rs112433998	snp	C/G	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63732051	CTGTCACCCAGGCTG[C/G]AGTGCAGTGGTGCGA	8925
rs112476291	snp	C/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63719468	CGGCCTTGCAGGCCA[C/G]TACAAGTCCTCCAGG	8925
rs112544777	snp	C/T	0.0123036	0.0774623	intron-variant	HERC1	GRCh38.p7	15:63806394	GTTGTAATCACCCTA[C/T]GCTCACCAACACAGA	8925
rs112579010	in-del	-/T	0	0	intron-variant	HERC1	GRCh38.p7	15:63822603	AAAAAAAAAAATTTT[-/T]AAATAATAATTGTAA	8925
rs112582885	snp	C/G	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63719433	AGACATCAGAGAGCT[C/G]GCTGGGGACCAGATC	8925
rs112593021	snp	C/T	0.211516	0.24702	intron-variant	HERC1	GRCh38.p7	15:63621500	TCTCGAGGAGTATCT[C/T]TGTGGCATTCTCTGT	8925
rs112681509	snp	C/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63753901	TACTCATGCCGGGCA[C/T]GGAGGTTCATGCCTG	8925
rs112721642	in-del	-/TGAC	0.0693013	0.172766	intron-variant	HERC1	GRCh38.p7	15:63784243	AAAATATTTTCAAAT[-/TGAC]TATTATCTAACAAAT	8925
rs112744626	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63618993	GCCCTTTATTTCCTT[C/T]TCCTGCCTGATTGCC	8925
rs112791137	snp	C/T	0.00349513	0.0416575	missense	HERC1	GRCh38.p7	15:63678139	CGGCTCTGAACCGAG[C/T]GGCTTTTCTTTAGCT	8925
rs112880368	snp	G/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63817097	CAGGGCAAACAACCT[G/T]CTTTCTTTTAAAAAA	8925
rs112898120	snp	A/G	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63650300	AGTCCCAGCTACCTG[A/G]GAGATGGAGGCTGCA	8925
rs112911550	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63693184	CTCTGTCTCAACAAC[A/C]ACAAAAAAAACCCAG	8925
rs112964926	in-del	-/T	0.476574	0.105661	intron-variant	HERC1	GRCh38.p7	15:63693248	GGAATTTTCTTTTTC[-/T]TTTTTTTTTTTTTGA	8925
rs112973474	snp	C/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63623494	ACAGATGGTGAGTCA[C/T]TGGTAGATGCCTAAG	8925
rs113010385	snp	A/G	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63617215	CCTTCCTGTGTCCAT[A/G]TGTTCTCATTGTTCA	8925
rs113023760	snp	A/C	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63712058	ATTAGCATCTTATTT[A/C]TCTTTACCCTAAATG	8925
rs113039303	snp	C/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63710999	GAAGTCATTGCAGGA[C/T]TCTGAGCAGAGAAAC	8925
rs113081937	snp	A/T	0.00119737	0.0244387	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834793	TGTACCTGGTTTTAC[A/T]CCTTTCCAGCCACCT	8925
rs113183225	snp	C/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63784762	ATAGGTGGCTGCCAC[C/T]GCATCCAGCTAATTT	8925
rs113192897	snp	A/G	0.115438	0.210697	intron-variant	HERC1	GRCh38.p7	15:63698400	TACAGCCTGGGCAAC[A/G]AGAGCGAAACTCCGT	8925
rs113207869	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63833029	CTCTAAGATAACATG[C/T]CTTTTACATAACCTC	8925
rs113208657	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63833747	GCAAAGCACACACGC[A/G]CGCGCGCACACACAC	8925
rs113246715	snp	C/G	0.0402882	0.136092	intron-variant	HERC1	GRCh38.p7	15:63653201	ATCCCAGCACTGTGG[C/G]AGGCCAAGGCAGGCG	8925
rs113277828	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63833341	GCCTCCACCCCGCTA[A/C]AGGCGGCCGGCGCCT	8925
rs113285909	snp	C/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63738742	TGGAACAATCTATCT[C/T]CAAGTATTCTTCTAA	8925
rs113310450	snp	C/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63615112	CCCTGACTAACCCAA[C/G]TAGAGTGGAGACGCT	8925
rs113406188	snp	C/T	0.0185938	0.0946107	intron-variant	HERC1	GRCh38.p7	15:63631685	AGCTGGGATTACAGG[C/T]GCCTGCCACCACGCT	8925
rs113430984	snp	A/G	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63820898	TACTACTACATTAAC[A/G]TTACTACCATTATCA	8925
rs113523730	snp	A/C	0.0520825	0.152737	intron-variant	HERC1	GRCh38.p7	15:63644400	CATTGGATTCTTAGC[A/C]TCTATAGAAAAAATA	8925
rs113525458	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63829465	GTGTGTGTGTGCACA[C/T]ATATGTTTATATAAA	8925
rs113535517	in-del	-/TTCGCCATA	0.172997	0.237846	intron-variant	HERC1	GRCh38.p7	15:63695230	CTGTAGAGACAGGGT[-/TTCGCCATA]TTTCGCCATATTGTC	8925
rs113580718	snp	A/G	0.0119091	0.0762411	intron-variant	HERC1	GRCh38.p7	15:63636365	AACCTCCACCTCCCC[A/G]GTTCAAGTGATTCTC	8925
rs113586071	snp	A/C/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63773105	GTTATTTTAACTAAA[A/C/T]AGATTTGTTGGTTGA	8925
rs113603860	snp	A/G	0	0	intron-variant	HERC1	GRCh38.p7	15:63647209	CAGTGAGCCAAGATC[A/G]CGCCACTGCACTCCA	8925
rs113616666	in-del	-/A	0.312593	0.242037	intron-variant	HERC1	GRCh38.p7	15:63728963	AAAAAAGAGCAGATT[-/A]TAAAAAATCTCACTT	8925
rs113715234	snp	C/T	0.00358779	0.0422022	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835542	TGCCCACTTTTTCTT[C/T]TTCTTTTTTTTGAGA	8925
rs113752258	in-del	-/A	0.268995	0.249277	intron-variant	HERC1	GRCh38.p7	15:63727559	AGCCTTAGGATAGAT[-/A]TAGACTCCAATGGAA	8925
rs113765742	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63741504	ATTTAGTAGATACGG[A/G]GTTTCACCATGTTAG	8925
rs113798263	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63631695	ACAGGCGCCTGCCAC[C/G]ACGCTCGGCTAATTT	8925
rs113801625	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63636333	TGGAGTGCAGTGGTG[C/T]GATCTCGGCTCACTG	8925
rs113824124	snp	C/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63697923	AGAACTATGGAAGAA[C/T]TGTGGACATGTTAAA	8925
rs113849113	snp	A/T	0	0	intron-variant	HERC1	GRCh38.p7	15:63655530	ATTATTATCTATGGT[A/T]AACTCAAATCATAAT	8925
rs113891103	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63833746	GGCAAAGCACACACG[C/T]GCGCGCGCACACACA	8925
rs114037445	snp	C/T	0.00676609	0.0577691	intron-variant	HERC1	GRCh38.p7	15:63782290	CTTGCTAAGGGCTAA[C/T]GAAGCTGGTGGACTT	8925
rs114042446	snp	A/G	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63650471	CAGGTTGGAGTGAGT[A/G]CAATGGCATGATCAT	8925
rs114055745	snp	A/G	0.0314385	0.121371	intron-variant	HERC1	GRCh38.p7	15:63676170	GCCTCCCAAACTGCC[A/G]GGATTACAAGTGTGA	8925
rs114059611	snp	A/C/T	0.0178098	0.0926698	intron-variant	HERC1	GRCh38.p7	15:63806750	CTTTGTTGTTGTAAG[A/C/T]TGGAACTCTGCCCAG	8925
rs114153979	snp	C/T	0.0607341	0.163335	downstream-variant-500B, intron-variant	HERC1, FBXL22	GRCh38.p7	15:63608148	TTCCACTTGGCTGCC[C/T]TCCCCACTGAGACAT	8925
rs114159254	snp	A/G	0.00309905	0.0392418	synonymous-codon	HERC1	GRCh38.p7	15:63694025	TTCTTCTTCTTCACC[A/G]TCTTCTTGCTCCCCT	8925
rs114168463	snp	A/T	0.0193772	0.0965046	intron-variant	HERC1	GRCh38.p7	15:63749263	ATGTTCAGAAGAGTA[A/T]TTTATGAACAAAGCA	8925
rs114223896	snp	A/G	0.0513262	0.151752	intron-variant	HERC1	GRCh38.p7	15:63818403	ATAAGGAGCCAAACC[A/G]ACAGATGGCAGACGA	8925
rs114227545	snp	A/C	0.0197687	0.0974348	intron-variant	HERC1	GRCh38.p7	15:63782837	AGAAGTTGATTCTAA[A/C]CCCTACGGATGACTT	8925
rs114228821	snp	A/G	0.0663309	0.169604	intron-variant	HERC1	GRCh38.p7	15:63825078	CTGTGGGAGGCCGAG[A/G]CAGGGAGATCACTTG	8925
rs114249214	snp	C/T	0.0498117	0.149749	intron-variant	HERC1	GRCh38.p7	15:63737678	AGCCACTGTGCCTGG[C/T]CAAGATAATTTTTTA	8925
rs114316120	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63657115	TATCGAACAGTTTTC[C/T]AAAGTGGTTATACCA	8925
rs114372804	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63825813	CTTGTCCCCCAGGCT[A/G]AGTATAGCGGTGGGT	8925
rs114459100	snp	A/C	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63720806	AATATTCAATTTTAA[A/C]AGCAAACTAAAGTAA	8925
rs114465843	snp	A/G	0.0349115	0.127424	intron-variant	HERC1	GRCh38.p7	15:63799501	CAAGACTCTGCCTCT[A/G]AAAAAAAAAAAATAG	8925
rs114468224	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63799962	GTGTGAGACTCCATC[A/T]TTACAGAAAAAAATA	8925
rs114504509	snp	C/T	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63647356	AAAAAACAACAGATG[C/T]CGGCAAGAAAGTGGT	8925
rs114509614	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63699600	TCATGTGCATATTTA[C/T]TGCAGGTTGTGAAAC	8925
rs114511841	snp	A/T	0.0652144	0.168387	intron-variant	HERC1	GRCh38.p7	15:63673220	AAAGTATTTATATAT[A/T]TTTTTTAATTGTTAA	8925
rs114514649	snp	C/T	0.0337553	0.125452	intron-variant	HERC1	GRCh38.p7	15:63695208	ACTTGGCTAATTTTT[C/T]GTATTTTCTGTAGAG	8925
rs114518520	snp	C/T	0.0130921	0.0798413	intron-variant, downstream-variant-500B	HERC1	GRCh38.p7	15:63668837	CACAGATTTCAACAA[C/T]ACTCTCTCAATAATA	8925
rs114554616	snp	A/G	0.000762309	0.0195083	synonymous-codon	HERC1	GRCh38.p7	15:63678051	CTCTGAGAGGTCAGC[A/G]AGGCCATGCCTAGTA	8925
rs114563781	snp	C/T	0.0103295	0.0711199	intron-variant	HERC1	GRCh38.p7	15:63730738	TTAGCGGCAGCCAGC[C/T]ATCTGCAATTTACTC	8925
rs114573741	snp	A/G	0.0333238	0.124705	intron-variant	HERC1	GRCh38.p7	15:63785403	AGCCTGGGCAATAAG[A/G]TGAGACAAAGTCTCT	8925
rs114578108	snp	A/C	0.02016	0.0983543	intron-variant	HERC1	GRCh38.p7	15:63784114	ACTCATAAAAATGAG[A/C]AAATTTCCAAAGGTT	8925
rs114589700	snp	C/T	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63712197	AATGTGGAAGGTGGG[C/T]ACAAGGCAAGAGGTG	8925
rs114598446	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63801862	CAAGGCTTTTACCTA[C/T]CTCATATGCTAATGA	8925
rs114651471	snp	C/T	0.0410537	0.137264	intron-variant	HERC1	GRCh38.p7	15:63688250	AGAATCTAGAGATTG[C/T]ATGGATAGAGAAATG	8925
rs114676043	snp	A/C	0.0352966	0.128072	intron-variant	HERC1	GRCh38.p7	15:63772617	AGAATCAGAAAACAA[A/C]GTTAGAAAAACATGT	8925
rs114696483	snp	A/G	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63803269	ATTTTCCAGGAAGGG[A/G]AGTGGAGGTACAGAG	8925
rs114797708	snp	A/G	0.0356815	0.128715	intron-variant	HERC1	GRCh38.p7	15:63764564	CCCCATGGGTATATT[A/G]CCCACCTGCCTTCCA	8925
rs114890690	snp	C/T	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63641925	TATTTCTTCAGAACC[C/T]GCAGAATAAGGCATC	8925
rs114997988	snp	C/T	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63718135	ACACAACCCCCTCCT[C/T]GGTTTTCACTTCTCT	8925
rs115009857	snp	C/T	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63740748	TCTACTCAGATTCTT[C/T]GTTCATTTTTAAAAC	8925
rs115011384	snp	C/G	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63693398	ACAGGCATGCGTCAC[C/G]ATGCCAGGCTAATTT	8925
rs115012264	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63723727	CGTTCAAAATGGAAT[A/G]ATATCCTCTTTGAGA	8925
rs115013514	snp	C/T	0.0648419	0.167978	intron-variant	HERC1	GRCh38.p7	15:63668348	AATTACAGAAATTAG[C/T]TGGGTGTGGTGGCAT	8925
rs115022440	snp	A/G	0.0418186	0.138422	intron-variant	HERC1	GRCh38.p7	15:63767150	GGATTACAAGTGCAC[A/G]CCACCATGCTTAGCT	8925
rs115027405	snp	C/T	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63820781	CCTTGGCCTCCCAAG[C/T]AGCTAGGACTATAGG	8925
rs115090520	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63724647	GTAGCCTGTCTAATC[C/T]AAATCATTATTTTAT	8925
rs115096615	snp	A/T	0.0119091	0.0762411	intron-variant	HERC1	GRCh38.p7	15:63801827	TTCATGTACATACAT[A/T]TTTGGATCCCAGCAA	8925
rs115118101	snp	G/T	0.0119286	0.0763022	intron-variant	HERC1	GRCh38.p7	15:63649959	TAACTAGTTTTTACT[G/T]AATTCTTAAAAAGAA	8925
rs115150012	snp	A/G	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63803120	TGAGATGGGAGGATC[A/G]CTTAAGCCTACGAGG	8925
rs115152653	snp	C/T	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63718164	CTAAGCTGAATATTT[C/T]TGATACTTTCTAGTC	8925
rs115153199	snp	G/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63754899	CACAGCACTTACCTT[G/T]TGTTGTCCTGTTTCA	8925
rs115201011	snp	C/T	0.02016	0.0983543	intron-variant	HERC1	GRCh38.p7	15:63683473	ACATTCAGTGGCTAA[C/T]GAGTTCTTATAAAAT	8925
rs115245190	snp	C/T	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63639273	TAAGATTATAAAACC[C/T]TATTTTTATTATATC	8925
rs115264323	snp	A/T	0.0150606	0.0854603	intron-variant	HERC1	GRCh38.p7	15:63744215	CTCTCCTCAGCCACC[A/T]AAAGCTGGGGGTGGA	8925
rs115276448	snp	A/G	0.0150606	0.0854603	intron-variant	HERC1	GRCh38.p7	15:63774313	AATAGTACTTGGCAT[A/G]TAGTAAATGTTTAAC	8925
rs115315686	snp	C/T	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63720329	TAACAATGTAGTATA[C/T]TCAGTAGATTTCAAA	8925
rs115431344	snp	C/T	0.0119091	0.0762411	intron-variant	HERC1	GRCh38.p7	15:63615108	TGGGCCCTGACTAAC[C/T]CAACTAGAGTGGAGA	8925
rs115476553	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63698492	GTTTGTAGGAGACAT[A/G]TGAAGACTTCTGAGT	8925
rs115507550	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63788821	ACTTGGAGGCTGGGG[C/T]AGGAGATCGCGCCAT	8925
rs115521816	snp	A/G	0.0659589	0.169201	intron-variant	HERC1	GRCh38.p7	15:63788547	ATAGCAAAACTTAAT[A/G]AAGCACAAAAAGTAC	8925
rs115559987	snp	G/T	0.0244538	0.107838	intron-variant	HERC1	GRCh38.p7	15:63646127	TATGGCTGTGATCAT[G/T]GTGCTCTTCTGATTT	8925
rs115606097	snp	A/G	0.00102646	0.0226313	synonymous-codon	HERC1	GRCh38.p7	15:63686425	TTTCCCTCCACTGCC[A/G]TGAGTTAAAATCTGT	8925
rs115611256	snp	A/C	0.0142736	0.0832652	intron-variant	HERC1	GRCh38.p7	15:63793145	AGAGGCGTCTGAACC[A/C]GAGCAACTCCATCTT	8925
rs115618219	snp	C/T	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63631342	ACTGCACTGAAATTC[C/T]ACTCTCAAAAGCCAT	8925
rs115627737	snp	G/T	0.0260105	0.111035	intron-variant	HERC1	GRCh38.p7	15:63822829	AGATTAGAAATGTAT[G/T]CAGAAAATAGAGCCA	8925
rs115630661	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63827832	AAGTACTGATACATG[C/T]TACAACATGGATGAA	8925
rs115660471	snp	G/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63654884	AAAAAAAAAAAAAAT[G/T]TATTATACAACAATC	8925
rs115677281	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63765075	AGAAGCTGCCTTTCC[C/T]TTTGTTCCGAAGCAG	8925
rs115728354	snp	C/G/T	0.0399052	0.1355	intron-variant	HERC1	GRCh38.p7	15:63683041	TTCGGGAGGCTGAGG[C/G/T]GGGAGAATCCCTTGA	8925
rs115732707	snp	A/G	0.00545444	0.0519372	missense	HERC1	GRCh38.p7	15:63648161	ATCCCACTGCAAATG[A/G]TCTGTCTTCACTGAA	8925
rs115739332	snp	A/G	0.0115144	0.0749975	intron-variant	HERC1	GRCh38.p7	15:63798416	TACCCTCTCCCACCT[A/G]CGTAACAGACACTTA	8925
rs115740478	snp	A/G	0.0345262	0.126772	intron-variant	HERC1	GRCh38.p7	15:63745276	CTGGTGTCTCAGTAT[A/G]TCACCTGCCCCTCTG	8925
rs115788175	snp	C/T	0.0663309	0.169604	intron-variant	HERC1	GRCh38.p7	15:63671334	CTATGACTGTGCTGC[C/T]GTAATCCAGTCTCAG	8925
rs115791239	snp	A/G	0.0707826	0.174302	intron-variant	HERC1	GRCh38.p7	15:63643713	CTGAATCAGTAATAA[A/G]ATATCAATCTGATTC	8925
rs115792169	snp	C/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63610190	CTTGAAATCAGCCCT[C/G]CTCCCCAGAGCCCAC	8925
rs115797572	snp	C/T	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63754785	GCAATATGAAAAACA[C/T]AATCATTTCTAACAT	8925
rs115845090	snp	A/T	0.0138799	0.0821421	intron-variant	HERC1	GRCh38.p7	15:63650047	ATTTCATAATAGCCT[A/T]CTAATGAATAAGACC	8925
rs115855854	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63710978	GACTTCTAGTCTGAG[A/G]AAAGGGAAGTCATTG	8925
rs115858521	snp	A/T	0.00636936	0.0560724	intron-variant	HERC1	GRCh38.p7	15:63777452	AATTTTGCTGTTTTA[A/T]ATTTGGCCAGTTTGA	8925
rs115860661	snp	A/C	0.0138799	0.0821421	intron-variant	HERC1	GRCh38.p7	15:63672236	ATCATAAGAGAGAGA[A/C]TGTTAGACTACTTGC	8925
rs115867188	snp	C/T	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63784570	CTTCACTGCATAAAT[C/T]TGAATTTCTTATATA	8925
rs115893480	snp	A/T	0.00835141	0.0640778	intron-variant	HERC1	GRCh38.p7	15:63812583	TGAGAATCTCTCAGG[A/T]TGACAAAAAATAAGC	8925
rs115907334	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63651633	GTCAATAAAGACATT[C/T]AAATTCTGTATGTGT	8925
rs115983877	snp	A/C	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63721141	GAAATATCAGAAAAT[A/C]CATCTTAGAAAGTAA	8925
rs115985909	snp	A/G	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63630297	TCTTTGGCCGCAGTC[A/G]AGAGAGAAAGACATA	8925
rs115995586	snp	A/G	0.0115144	0.0749975	intron-variant	HERC1	GRCh38.p7	15:63791125	GACATACAGAAATTT[A/G]CAGTTTGGGGATAAA	8925
rs116040183	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63660253	TGAACCTGGGAGGCC[A/G]TGGCTGCAGTAAGCT	8925
rs116041887	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63743613	AAAGGATTCTGAGGC[A/C]TTCTTCAAAATGTCA	8925
rs116045619	snp	C/T	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63780776	AAGACCGAGCACAGC[C/T]ACTACATCAACATCT	8925
rs116100168	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63764997	GTGAAAAGGAAATAA[A/G]ACCTTGAGACTCCAA	8925
rs116103211	snp	A/G	0.0162398	0.0886349	intron-variant	HERC1	GRCh38.p7	15:63755751	GCACCACTGCACTCC[A/G]GCCTGGGTGACAAAG	8925
rs116143018	snp	C/G	0.0391387	0.134304	utr-variant-3-prime	HERC1, FBXL22	GRCh38.p7	15:63608628	CACGCTCCAATTCCT[C/G]AATCTGCTTTATTTC	8925
rs116145276	snp	C/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63717665	CTCCTCACTCCAGGA[C/G]TTCAAAACCAGCCTG	8925
rs116147545	snp	A/G	0.00447584	0.0470944	intron-variant	HERC1	GRCh38.p7	15:63661724	AGGTATCTTCAGGAG[A/G]TCTGGATATCTACAC	8925
rs116150899	snp	C/G	0.0402882	0.136092	intron-variant	HERC1	GRCh38.p7	15:63769956	TCCCCTCACATTTGT[C/G]TGCTTAAGATATTCA	8925
rs116174450	snp	A/G	0.0182284	0.0939223	intron-variant	HERC1	GRCh38.p7	15:63648351	AGACAAAATGTAGGC[A/G]TACAGTGGGGATTCC	8925
rs116209745	snp	A/G	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63793502	GGAACCCTCAGTTTC[A/G]GGAATTGCCCACCCC	8925
rs116210803	snp	A/C	0.0138799	0.0821421	intron-variant	HERC1	GRCh38.p7	15:63828067	TGCACCATCTTGTGA[A/C]TATACTAGAAACCAC	8925
rs116238605	snp	A/C	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63611953	ACTTTGGGAGGCCAA[A/C]GTGACCAGATCACCT	8925
rs116242351	snp	C/T	0.0158469	0.0875917	intron-variant	HERC1	GRCh38.p7	15:63720007	TAAGTGGGTAAGAAA[C/T]GAAACAACATTTCTT	8925
rs116251656	snp	A/G	0.0524604	0.153226	intron-variant	HERC1	GRCh38.p7	15:63751733	CTTTATTTTTTTCAC[A/G]CATATATATTTGATT	8925
rs116277574	snp	C/T	0.0150606	0.0854603	intron-variant	HERC1	GRCh38.p7	15:63804156	ATTCACAGACCGAAA[C/T]GTAAGAGCTAAAACT	8925
rs116310927	snp	C/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63832308	ATACATATATACGTA[C/G]ATTTATGCATAAGAC	8925
rs116326284	snp	A/G	0.00467641	0.0481283	intron-variant	HERC1	GRCh38.p7	15:63628859	TTCAATTAGAAAGAG[A/G]AAGAGAGGAAGTCAA	8925
rs116338011	snp	C/G	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63822795	AACCAGAATAAGGCA[C/G]AGATGACAAAATGTG	8925
rs116375944	snp	A/C/T			intron-variant	HERC1	GRCh38.p7	15:63712910	CCTGTCTCACATGTA[A/C/T]AAAAAAAAAAGTTTT	8925
rs116391963	snp	A/C	0.0345262	0.126772	intron-variant	HERC1	GRCh38.p7	15:63691612	TTCTTTATCCTCTTG[A/C]AACTTAATATAAGCC	8925
rs116393001	snp	C/T	0.0138799	0.0821421	intron-variant	HERC1	GRCh38.p7	15:63647998	CTCTGACTTCTCCAC[C/T]GTGTAATCTATGCAT	8925
rs116429346	snp	A/G	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63787601	AAGAATGACTTTGAT[A/G]GGTCAAACTATTATA	8925
rs116455805	snp	A/G	0.000550179	0.0165767	intron-variant	HERC1	GRCh38.p7	15:63664455	CAAAGAAAAGGATAC[A/G]GAACATAAAATTACC	8925
rs116458080	snp	A/G	0.00676609	0.0577691	intron-variant	HERC1	GRCh38.p7	15:63719387	AGGCCAGTGTGGCTG[A/G]GGCAAACCGTGCATG	8925
rs116484115	snp	C/T	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63642272	ATTTGAAAGCCAAGA[C/T]ATATTTTGTATACTT	8925
rs116543356	snp	A/G	0.0150606	0.0854603	intron-variant	HERC1	GRCh38.p7	15:63672041	AAGACATGCCCTTTC[A/G]TTTGAAAAGCAGACT	8925
rs116549442	snp	A/G	0.0162398	0.0886349	intron-variant	HERC1	GRCh38.p7	15:63773065	ACTTGAAATATACAT[A/G]TATCATTTATAAGTG	8925
rs116611386	snp	C/G	0.00676609	0.0577691	intron-variant	HERC1	GRCh38.p7	15:63687206	CAGGATGAAGGCAGA[C/G]AGACTGACTAATCAG	8925
rs116677296	snp	A/G	0.00953873	0.0683987	intron-variant	HERC1	GRCh38.p7	15:63770884	TCTCAGACAACAGTA[A/G]AGTGTAAGAAACATG	8925
rs116705267	snp	C/T	0.0659589	0.169201	intron-variant	HERC1	GRCh38.p7	15:63794267	TTTCACTTTACTCTA[C/T]AGACTCGCCCTGAAT	8925
rs116729248	snp	C/T	0.0158469	0.0875917	intron-variant	HERC1	GRCh38.p7	15:63633346	CATAAAACAATCACA[C/T]AGAAGGACTTCTGTA	8925
rs116739150	snp	G/T	0.0134861	0.0810011	intron-variant	HERC1	GRCh38.p7	15:63820791	CCAAGTAGCTAGGAC[G/T]ATAGGCATGCCACCA	8925
rs116800120	snp	A/G	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63748464	GCCCCTCTGGTTCTA[A/G]GAGTCCAGAAAATAT	8925
rs116885486	snp	C/T	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63762803	CTCTTCACAAAAATA[C/T]TGCAACTAATTGTTG	8925
rs116890874	snp	C/T	0.0228947	0.104514	intron-variant	HERC1	GRCh38.p7	15:63826994	TCACACTTACAGAAA[C/T]CTACCTTGAAGATAC	8925
rs116892342	snp	A/G	0.0142736	0.0832652	intron-variant	HERC1	GRCh38.p7	15:63822789	GGTTTAAACCAGAAT[A/G]AGGCAGAGATGACAA	8925
rs116923934	snp	A/T	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63644129	ATTAGTGAGTTGGCT[A/T]CTCCTTCCCTCCCTC	8925
rs116967176	snp	A/G	0.0282622	0.115466	synonymous-codon	HERC1	GRCh38.p7	15:63774787	GCCTTTCTCCATGGT[A/G]TGTACAACTGCCGAA	8925
rs117036717	snp	A/G	0.0218588	0.102233	intron-variant	HERC1	GRCh38.p7	15:63656399	ATGGATAAAGAAAAT[A/G]GATTTCTTAAGGGAC	8925
rs117039403	snp	C/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63759789	GAAGTCAACATATTA[C/G]TTTGCTAGCACATGA	8925
rs117044596	snp	A/G	0.0256215	0.110247	intron-variant	HERC1	GRCh38.p7	15:63710067	ACTACTATGGCAAAA[A/G]TGCAGACCACTGCAG	8925
rs117062127	snp	C/T	0.0193772	0.0965046	intron-variant	HERC1	GRCh38.p7	15:63665825	TATTTATCAACTTTA[C/T]ATACAATTAGAAGCA	8925
rs117148149	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63736073	CCCAGAATGGAAAGG[A/G]AAAAACAGCATCAAA	8925
rs117185859	snp	A/G	0.0298908	0.118541	intron-variant	HERC1	GRCh38.p7	15:63814602	GCTGGGATTACAGGC[A/G]TGCACCATCACATCC	8925
rs117213271	snp	A/G	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63722907	ACCCGCGGATATGGG[A/G]AGACTACTATACTTC	8925
rs117214067	snp	A/G	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63693818	CTAAATCATATATAC[A/G]TGAAGAGAAAAGAGG	8925
rs117250066	snp	C/T	0.00874735	0.0655527	intron-variant	HERC1	GRCh38.p7	15:63728735	GGGGAGCAAAGAGGA[C/T]AGAAGGCAAAATTCG	8925
rs117254643	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63657914	TGCTCTACAGTGTGA[A/G]CCACTGTCATAAATC	8925
rs117275825	snp	A/T	0.00597247	0.0543191	intron-variant	HERC1	GRCh38.p7	15:63751232	ACTGTAACTTTTCTA[A/T]GTTTAGATATGTTTA	8925
rs117293288	snp	C/T	0.0154538	0.0865337	intron-variant	HERC1	GRCh38.p7	15:63726751	AAATTCTTCTAAAAC[C/T]TCAGGAAGAGATAAC	8925
rs117302683	snp	C/T	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63795540	TGATACAAAAGGTTC[C/T]TATTTTGAATTACTC	8925
rs117317564	snp	C/T	0.0185938	0.0946107	intron-variant	HERC1	GRCh38.p7	15:63698252	GAAACTTTGTCTCTC[C/T]TAATAATACAAAAAA	8925
rs117356077	snp	C/T	0.0150606	0.0854603	intron-variant	HERC1	GRCh38.p7	15:63697125	AAACCTAAAGTAAAA[C/T]AGTATTAATTAAAAG	8925
rs117359339	snp	C/T	0.0134861	0.0810011	intron-variant	HERC1	GRCh38.p7	15:63638038	AAGGGTTTGGCGCTA[C/T]ATCGTACCAGGATTA	8925
rs117394050	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63614223	CAACCCTCAGAAGAA[A/G]GGTCATCAGAAAAGC	8925
rs117400957	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63614247	GAAAAGCCTGGACAC[C/T]ATCTTAGAGCCTGGT	8925
rs117407232	snp	A/G	0.0115144	0.0749975	intron-variant	HERC1	GRCh38.p7	15:63707652	GACAAAACAAGGCCG[A/G]GAGTGGTGGCTCACA	8925
rs117428071	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63622071	TTAATTTACAAGTCC[A/G]TGAAACAGGATCCAA	8925
rs117445496	snp	A/C	0.00993419	0.0697739	intron-variant	HERC1	GRCh38.p7	15:63828687	AAGCAGTGTTTAGTA[A/C]CTATAATGTTTCATA	8925
rs117586333	snp	C/T	0.0236746	0.106192	intron-variant	HERC1	GRCh38.p7	15:63771778	CCCAATAAGGAGCTA[C/T]ATTATAGGGTATGGC	8925
rs117598128	snp	C/T	0.0165278	0.0893908	intron-variant	HERC1	GRCh38.p7	15:63815257	CTAATTTATATTTCA[C/T]GCTCTCCACCTTCCA	8925
rs117601032	snp	C/T	0.0279526	0.114869	intron-variant	HERC1	GRCh38.p7	15:63630311	CGAGAGAGAAAGACA[C/T]AACTAGACTTACAAA	8925
rs117602042	snp	C/T	0.0422008	0.138995	intron-variant	HERC1	GRCh38.p7	15:63817321	GTATGATAATGTTAT[C/T]ATGGTTATGCTATAA	8925
rs117660857	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63632200	CTTCAGTCATGGTTT[A/G]CTTCCTCTTCCTCAC	8925
rs117707716	snp	A/G	0.0138799	0.0821421	intron-variant	HERC1	GRCh38.p7	15:63697371	TACAGTGGAATTATG[A/G]ATTTGGGGGAAGAAT	8925
rs117721499	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63756995	TTGTCCAGGTTATGA[C/T]TGAATGAAACAACAA	8925
rs117726434	snp	C/T	0.0111196	0.0737302	intron-variant	HERC1	GRCh38.p7	15:63691113	CTCTCCGTCCATGCA[C/T]TGACTGTCTCACAGG	8925
rs117760756	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63800943	AGACCTCAAGGGAGA[C/G]GAAAAGGGGTGGAGA	8925
rs117762519	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63776670	ACAGGTTGCGCATTT[C/G]TTAAAACCTAGTGGG	8925
rs117786985	snp	C/T	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63722895	TTGGAACACATCACC[C/T]GCGGATATGGGGAGA	8925
rs117819852	snp	A/G	0.0295035	0.117819	intron-variant	HERC1	GRCh38.p7	15:63711427	GAATCTCACTAGACT[A/G]TAAGACTGGGAGTAT	8925
rs117844515	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63613208	TGAAAAAAGCAGATA[C/T]TGCTGCTCTCATGTG	8925
rs117856030	snp	C/T	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63764456	TTATTCCAAGGGACA[C/T]AGGGCTCTCGAAACA	8925
rs117894525	snp	A/G	0.00438332	0.0466095	intron-variant, downstream-variant-500B	HERC1	GRCh38.p7	15:63669110	AGCAGTAACAAAACG[A/G]TATCTAGAAAATCCC	8925
rs117960804	snp	C/T	0.0119091	0.0762411	intron-variant	HERC1	GRCh38.p7	15:63806630	CAAGGGCTCAGAACA[C/T]TGTAGAAGAGGAATT	8925
rs117972734	snp	A/G	0.0165278	0.0893908	intron-variant	HERC1	GRCh38.p7	15:63747646	AGTAAGTCAAAACTC[A/G]AAAGGAATAATTTAT	8925
rs117994834	snp	A/C	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63786005	GCCACCATGCCCAAC[A/C]CAAGAGATAATTCTT	8925
rs118019608	snp	A/C	0.00279162	0.0372561	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834811	TTTCCAGCCACCTTC[A/C]TGGTGTCTTTCCTTC	8925
rs118030403	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63686819	ACATAAAAGTGTGTC[C/T]AACCATGCTTGAGAA	8925
rs118046941	snp	A/G	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63610753	ACACTTAAACTGGCA[A/G]GAAGGGCCTGTGTGT	8925
rs118053000	snp	A/G	0.0622301	0.165053	intron-variant	HERC1	GRCh38.p7	15:63733648	CGCTTGAGTCCAGGA[A/G]TTCAAGACCAGCCTG	8925
rs118053682	snp	A/G	0.0279526	0.114869	intron-variant	HERC1	GRCh38.p7	15:63816933	CCTTACATATCTCCC[A/G]ATGGAAACAAAAATC	8925
rs118083377	snp	A/G	0.0165278	0.0893908	intron-variant	HERC1	GRCh38.p7	15:63652798	CTGGATTACAGGCAC[A/G]TGCCACCACAACTGG	8925
rs118084831	snp	C/G	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63627256	AATCTTAGGACCCCC[C/G]CTAAGAAATAGAGGG	8925
rs118110594	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63679900	CATGAAATAGTGCCT[C/T]AATATTAATATATCG	8925
rs118127176	snp	C/T	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63638130	AGAGAAAATCACTAA[C/T]TAGGAGTATCTAAAC	8925
rs137865338	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63641987	CTACAAGGATAGCTG[C/T]AAAAGAGGTAGCACT	8925
rs137898069	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63681544	CAACACTGGCCTTTG[A/G]CTAGGACCTGGGAAT	8925
rs137911679	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63771450	AGTTTTTTTTTTTTT[-/T]GAGACAGTCTTGGTC	8925
rs137916365	snp	A/C	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63783805	GGGTGCAGTGGCTCA[A/C]ACCTGTAATCCCAAC	8925
rs137926425	snp	C/G	0.0209368	0.10015	missense	HERC1	GRCh38.p7	15:63749706	ACTATTCTTGTGGCA[C/G]CCAGTTCTTCAATAA	8925
rs137927318	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63793802	GTTCCCTGTGTTAGA[A/G]ATGTGTGAACCAAAG	8925
rs137929537	snp	G/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63709511	CACAGTTGAGGCAAG[G/T]ACAACAGGCATTATT	8925
rs137931546	snp	C/T	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63676611	AAATATAAAAATTAG[C/T]CGGGCATGATGGTGG	8925
rs137967909	snp	C/T	0.0103295	0.0711199	intron-variant	HERC1	GRCh38.p7	15:63818875	AAAACCACTTCAGTA[C/T]TACTGCAGCCTACTA	8925
rs137979147	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63722246	TACCATGGTACTTAA[C/T]AGTATATCTTATCTC	8925
rs137982534	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63648867	TTCTGTTAATGGAAT[A/G]CCATGTAAGCAGGCA	8925
rs138008572	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63736136	AACTGACTTAAAAGA[C/T]CTGAAATGGCTACAC	8925
rs138014399	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63663508	TCACTCAAGCTGGAG[C/T]GCAATGGCACAATCC	8925
rs138041862	snp	C/T	0.0111196	0.0737302	intron-variant	HERC1	GRCh38.p7	15:63779395	AAAAAGCAAAAGAAT[C/T]AGCCAGGCATTATTT	8925
rs138052173	snp	C/T	0.000580821	0.0170315	missense	HERC1	GRCh38.p7	15:63674768	GTTGGGATTCCACAC[C/T]TGGCAGTGTTGGATC	8925
rs138067068	snp	A/C	0.00279162	0.0372561	downstream-variant-500B, utr-variant-3-prime	HERC1, FBXL22	GRCh38.p7	15:63608339	TGGTACTGAGAGGGG[A/C]GGAGCAGCTGAGGGA	8925
rs138069909	in-del	-/A	0.0667028	0.170006	intron-variant	HERC1	GRCh38.p7	15:63734008	CGCTATAAAAATAAG[-/A]AAAAAAAAATTAGCC	8925
rs138073059	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63708628	TAACAGTAGATAACA[C/T]GTCATATAATACATT	8925
rs138082820	snp	A/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63636435	GCCACCATATCTGGC[A/T]AATTTTTGTATTTTT	8925
rs138136662	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63705225	GTGGCATGATCACAG[C/T]ACCCTGCAACTTCGA	8925
rs138157339	snp	A/G	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63804535	AAGTTGCAGTGAGCC[A/G]AGATCGTACCATTGC	8925
rs138179660	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63695687	GCCACCACGCCCGGC[C/T]GAGTCTGTATAATCT	8925
rs138188749	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63814193	ACAACTATACATCAT[A/C]ATTTAACAATGATTA	8925
rs138208471	snp	A/G	0.0279526	0.114869	intron-variant	HERC1	GRCh38.p7	15:63622494	TGTGCCACCATGACC[A/G]GCTAATTTTTGCATT	8925
rs138229811	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63810320	GGTGTATACACATAC[A/T]CTGAAATAGTACTCA	8925
rs138239424	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63735710	AGATAAACTCCATAG[C/T]GCCTGTCAGTTCTAA	8925
rs138244233	snp	A/C/T	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63724060	TTTTTCTAATACATA[A/C/T]AAGTAAACAAAATAA	8925
rs138247230	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63764452	TGATTTATTCCAAGG[C/G]ACACAGGGCTCTCGA	8925
rs138299515	snp	A/G	0.0103295	0.0711199	intron-variant	HERC1	GRCh38.p7	15:63832071	ACAACAACCCCAGAT[A/G]ACAATCTATCCTATT	8925
rs138304970	snp	G/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63732385	ATTCCAGCAGTAAGA[G/T]GCTGAGAAGAAACCA	8925
rs138312899	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63657807	AACTATTTGCTTTAT[A/G]TAGTTTGAGGTTGGG	8925
rs138313726	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63821930	ACCAGGTAGGCAAGT[A/G]ATTCTATTTCAGGAA	8925
rs138315780	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63755591	CGAGTTCAGCCTGGG[A/C]AACATGGCAAAACCC	8925
rs138325997	snp	A/G	0.0150606	0.0854603	intron-variant	HERC1	GRCh38.p7	15:63652870	GGCCAGGCTGGTCTC[A/G]AATGCCTGGCCTCAA	8925
rs138356587	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63705561	TTTTTTTCTATGGAT[A/G]AGAAACCTAACATTC	8925
rs138360051	snp	A/C	8.31207e-05	0.0064462	synonymous-codon	HERC1	GRCh38.p7	15:63612344	CCTCATGAAAAGCAC[A/C]CGCTCCTCATTGGAG	8925
rs138371120	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63772798	ATCCCAAACAAAGCA[C/T]GGCATGCTTTTCTTA	8925
rs138372887	in-del	-/AC	0.0244538	0.107838	intron-variant	HERC1	GRCh38.p7	15:63755131	CTAACAAAATAAATG[-/AC]AGTCTTTGGCCTAGT	8925
rs138392113	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63743949	TGGGCTTTCCAGATA[C/T]TTTAAAGGACTTGGG	8925
rs138407982	snp	C/G	0.000234146	0.0108175	intron-variant	HERC1	GRCh38.p7	15:63645440	GATAACAGTCTATAC[C/G]AATATAAAAACTAAG	8925
rs138435265	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63759708	ACTACAGTGACTATC[A/T]ATTTGTTTTCTGCCT	8925
rs138447978	snp	C/T	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63689916	TGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCTGA	8925
rs138449209	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63685330	TGGGGGCAGGTCACA[C/T]TGGTATCATGTTAAC	8925
rs138474828	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63629304	AGTCCTCACAGCTCC[A/G]ACTGCTAAAAACTAA	8925
rs138494647	snp	C/T	0.0162398	0.0886349	intron-variant	HERC1	GRCh38.p7	15:63619557	TATTGATTGGAATAG[C/T]TTCAGAAGGAATGGT	8925
rs138495818	snp	C/T	0.0182019	0.0936463	intron-variant	HERC1	GRCh38.p7	15:63685505	TTGTCCAGTGCTAAA[C/T]TGATGACTAATCTAC	8925
rs138508562	snp	C/T	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63676052	GGGATTACAGGCGCA[C/T]GCCACTACGGCTGGC	8925
rs138526510	snp	G/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63797706	CTTCCTTTACTGCAA[G/T]GTAGTGGTCTCTGTT	8925
rs138534091	snp	A/G	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63726949	CCTTACTCACCTGAT[A/G]GACTGAATCTTAGCA	8925
rs138535952	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63791806	AGAATAAAGAAGTTG[A/G]TATTTCTTCAAATAT	8925
rs138540333	snp	G/T	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63671130	ATCGCTTGAACTCAG[G/T]AGGCTGAGGTTACGG	8925
rs138563290	snp	A/C/T	0.00199481	0.0315187	intron-variant, missense	HERC1	GRCh38.p7	15:63702141	AATTAAACATGCCAT[A/C/T]ATGTACTTGCTTGAA	8925
rs138574651	snp	A/G	0.0640965	0.167152	intron-variant	HERC1	GRCh38.p7	15:63788778	AAAAATTAGCTGGGC[A/G]TGGTGGCAAGTGCCT	8925
rs138580960	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63713072	AATAATTTGCATGTC[A/C]CTAAACTACAGAGCA	8925
rs138587385	snp	A/T	0.00795532	0.062565	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834945	GAGAAGCACACAAAC[A/T]TACAAGCCATGAATG	8925
rs138592904	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63809526	GGAGCTGTGGATAAC[A/G]CTAAGATAATGAAGA	8925
rs138610041	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63641078	TCTAATAAGTGGAGA[C/T]GATATTCAGTCTGAT	8925
rs138620185	snp	C/T	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63821426	CCAGGCATGGTGGCA[C/T]GCACCTGTAGTCCCA	8925
rs138630046	in-del	-/AG	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63803937	GTGGTACTTTCATCA[-/AG]ATAGATCAACAGAAC	8925
rs138670714	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63814786	CATTAGCTTTCAAGA[C/T]GCAGAAAATTTAAAT	8925
rs138675762	snp	C/T			upstream-variant-2KB	HERC1	GRCh38.p7	15:63835273	CATATTAAGTACTCA[C/T]TAAATGATGGGTCTT	8925
rs138677296	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63731793	ACTCTGATCCTGTAA[A/G]TGCTGATGAGTACAG	8925
rs138721064	snp	A/C/G	0.00438476	0.0466401	intron-variant	HERC1	GRCh38.p7	15:63615469	AAAAAGATTAGCTAG[A/C/G]CGTGGTGACACATGC	8925
rs138766959	in-del	-/TCTT	0.0648419	0.167978	intron-variant	HERC1	GRCh38.p7	15:63743570	GCCCAGCTCACTAAG[-/TCTT]TCTTCTGCCATCAAT	8925
rs138779687	snp	C/T	0.00636936	0.0560724	intron-variant	HERC1	GRCh38.p7	15:63741688	TATGATGTAAGGGGC[C/T]AACTTCATTCTTTTG	8925
rs138788434	in-del	-/TCTCTC			intron-variant	HERC1	GRCh38.p7	15:63744165	GTGTGTGTGTGTGTG[-/TCTCTC]TCTCTCTCTCTCTCT	8925
rs138791841	snp	A/T	0.0170251	0.090679	intron-variant	HERC1	GRCh38.p7	15:63668531	CTAACTACTACAACA[A/T]GCTGCCTTTACCCAT	8925
rs138793895	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63657532	CTTTACACATTCTGT[C/T]GGTTAGATGCATTAC	8925
rs138821975	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63772488	ACATGTGACCATAAA[C/T]ACATTATTTTATTGT	8925
rs138828182	snp	A/G	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63701389	ACCAAAATATTCTAT[A/G]GAATGGCTGACGAAG	8925
rs138849923	snp	C/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63739497	CCACTGCACCCAGCC[C/T]ACTAAGGTATTGCTA	8925
rs138854741	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63807799	CTACCTTTGTGCCCC[C/G]ACTCATGCTGTTGTC	8925
rs138855321	snp	A/G	0.000156985	0.00885819	intron-variant	HERC1	GRCh38.p7	15:63665880	GGGGCTTTGAAATTT[A/G]TAACACATGGAACAA	8925
rs138855490	snp	A/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63768781	CTGGCTCTTACTGAA[A/T]GGGTCTCATCCTGAG	8925
rs138861642	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63696430	TTTTTAACACTTAGA[A/C]AATTCTGACATTTCA	8925
rs138912779	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63783144	AGAGGACTGACTCCT[C/T]TTGAATTTTGAAAGA	8925
rs138916852	in-del	-/T	0.02016	0.0983543	intron-variant	HERC1	GRCh38.p7	15:63813862	ACCTGAGGTCAGGAG[-/T]TTTGAGACCAGCCTG	8925
rs138932031	snp	A/G	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63792722	AGATTTTCTCCACAC[A/G]CCAAGCAAGCAATCT	8925
rs138962471	in-del	-/T	0.309963	0.242702	intron-variant	HERC1	GRCh38.p7	15:63649707	TCCGTCAGCTAGACG[-/T]GTAAGTGCAGTCATT	8925
rs138983524	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63800692	ATATATAATTTGTGC[A/G]ATTTGTTTAATGTCC	8925
rs138991623	in-del	-/TGTCTC			intron-variant	HERC1	GRCh38.p7	15:63744163	GTGTGTGTGTGTGTG[-/TGTCTC]TCTCTCTCTCTCTCT	8925
rs139079538	snp	G/T	0.0287284	0.116357	intron-variant	HERC1	GRCh38.p7	15:63613162	CTAACTCCCAGCTCT[G/T]CCAATTATTAACTCT	8925
rs139115203	snp	A/G	0.0166325	0.0896639	intron-variant	HERC1	GRCh38.p7	15:63775766	AATGCAGCCGGGTGC[A/G]GTGGCTCACGCCTGT	8925
rs139124421	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63638082	GTGGTCGATAAAATC[C/T]GGCTAAAGATCCTAG	8925
rs139175515	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63608912	AATCACAGAAAAATA[A/G]AAACATCTAATTTCT	8925
rs139189404	snp	C/G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63728863	GTGACTACACAGAAG[C/G/T]CCAAAGAAAGAATTT	8925
rs139192703	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63653709	ACAGAATGTAAATAC[C/T]ATGTAAACAGTTATA	8925
rs139200162	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63726038	TCAGGCTGGAGTGCA[A/G]TGGCATGATCTTGGG	8925
rs139212149	snp	C/G/T	3.65994e-05	0.00427769	missense	HERC1	GRCh38.p7	15:63652417	GTTAGCACTCACAAT[C/G/T]TGTTGAACACACAGG	8925
rs139223552	snp	A/G	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63769719	AAATTAGCCAGGCAT[A/G]GTGGCGGGCACCTGT	8925
rs139247366	snp	C/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63744429	GTGTCCTTCCCTTCA[C/G]GGGGAGTGAGGTCCC	8925
rs139251249	snp	A/C	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63816487	GTAACTACTGCCCTG[A/C]ACAAATTACTTTTGA	8925
rs139254869	snp	C/T	0.02016	0.0983543	intron-variant	HERC1	GRCh38.p7	15:63691419	TGCAGTGAGTTGAGA[C/T]CACACCACTGCACTC	8925
rs139256681	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63647231	TGCACTCCAGCCTGG[A/G]CGAAAAAGCTAGACT	8925
rs139258279	snp	C/G	9.09959e-05	0.00674461	intron-variant	HERC1	GRCh38.p7	15:63746868	GTATAGCTAAAATCT[C/G]AGAGAAAGACGTGGT	8925
rs139264101	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63723020	ATAGTTACACTATTT[G/T]CCACAAAGGGAAAAA	8925
rs139265743	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63646567	AACACTTTGGGAGGC[C/T]GAGGTGGGCGGATCA	8925
rs139276078	snp	A/G	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63649147	ATCACAAGGTGAGGA[A/G]ATCGAGACCATCCTG	8925
rs139294423	snp	C/T	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63761551	ATGATCACAGCACTG[C/T]ACACTCTAGCCTGGG	8925
rs139299732	snp	C/T	0.0494327	0.149241	intron-variant	HERC1	GRCh38.p7	15:63687136	ACAGAATGATGTATA[C/T]AGGAGATCTCTGATC	8925
rs139313347	snp	C/T	0.0298908	0.118541	intron-variant	HERC1	GRCh38.p7	15:63630863	TTTATTCATAAAAAT[C/T]TTTTAAAAAGTTGTA	8925
rs139313516	snp	G/T	0.0700422	0.173537	intron-variant	HERC1	GRCh38.p7	15:63762514	ATTTTTAATAGAGAC[G/T]AGGTTTCACCATATT	8925
rs139315502	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63801635	AGCTCAATAAATATT[G/T]CCTGAATTAAGCTAA	8925
rs139323548	snp	C/T	0.0162398	0.0886349	intron-variant	HERC1	GRCh38.p7	15:63687403	ATTAGTCAGGTGTGG[C/T]GGCAGGTGCCTGTAA	8925
rs139326996	snp	C/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63831156	GTGTCTCCCAGGCTG[C/G]AGTAGAGTGGTGCAA	8925
rs139329223	snp	A/G	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63798377	ACAATCAGGAATTAA[A/G]GTGTTTTCCAGGTAA	8925
rs139330705	snp	A/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63765183	TACTGAGCGCCAGAG[A/T]AATACATAATTCCAC	8925
rs139368600	snp	A/G	0.0209421	0.100162	intron-variant	HERC1	GRCh38.p7	15:63714513	GCACAAATTTGGAGC[A/G]AAGACAGTATTCTTC	8925
rs139372260	snp	A/G	0.00162911	0.0284938	intron-variant	HERC1	GRCh38.p7	15:63643597	ATAAAGATAAATTAT[A/G]TAAGTTCAAGATTTA	8925
rs139382130	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63799006	GTTGACTTTTTTAAA[A/G]CGTCATCTCTGGGCT	8925
rs139393353	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63827757	TGTACCTCAACTGAC[A/G]CATGAACAAAATGTA	8925
rs139401511	snp	A/G	0.0490535	0.14873	intron-variant	HERC1	GRCh38.p7	15:63760412	TGCCACTGTACTCCA[A/G]CCCGGGCAGCAGAGA	8925
rs139454336	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63806018	CCAATGCTGGTATTC[C/T]CAAAAGTTCTAGAAC	8925
rs139461010	snp	C/T	0.0140251	0.082558	intron-variant	HERC1	GRCh38.p7	15:63626198	AAGGAAACAGCATTG[C/T]TTTCACTTTTCACAT	8925
rs139467237	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63736927	ATCACACTCTTACCC[A/G]TGATTGGCTTCGAAG	8925
rs139522211	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63802643	AAATCCAAACTGACA[C/T]ACATACATAAATTAC	8925
rs139538463	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63737418	ATATATATATATATC[G/T]TTTTTCCAGATATAT	8925
rs139613398	snp	A/G	0.0260105	0.111035	intron-variant	HERC1	GRCh38.p7	15:63692102	CCAAGAAGCAAGGTC[A/G]GAATCTGTGCTAAAA	8925
rs139648855	snp	A/G	0.0182019	0.0936463	intron-variant	HERC1	GRCh38.p7	15:63627495	CCTGGCCAATATGGC[A/G]AAACACCATCTCTAC	8925
rs139650646	snp	C/T	0.0119091	0.0762411	intron-variant	HERC1	GRCh38.p7	15:63727994	TGTAGTATCAGTGTT[C/T]ATTCACTTTCAGAAA	8925
rs139652183	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63801789	TAGGGATTCTATCTG[C/G]AGTCCACTTCAGTCT	8925
rs139654760	snp	A/T	0.00676609	0.0577691	intron-variant	HERC1	GRCh38.p7	15:63671984	AAGCATCACTTGGAA[A/T]TTACAAACCTATTAA	8925
rs139656203	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63630364	GATGTGCTTGGAGTA[C/T]TGCAGTAGATTATGA	8925
rs139692386	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63785639	GCCAGGAATGGTGGC[A/G]CATGATGTGGTCCCA	8925
rs139697771	snp	G/T			missense	HERC1	GRCh38.p7	15:63732979	ATTTCAGCCAGGTGG[G/T]TATCTGGATGGCAGC	8925
rs139700911	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63612864	CCTGATGCCAGCCCC[A/G]CTCACTCATATTCCT	8925
rs139702436	snp	C/T	0.0138799	0.0821421	intron-variant	HERC1	GRCh38.p7	15:63683059	GAGAATCCCTTGAAA[C/T]TGGCAGGTGGAGGTT	8925
rs139702976	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63789607	GTTCGAGACCAGCCT[C/G]GCCAACATGGTGAAA	8925
rs139708330	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63740643	AGTGGTATCTCAGTG[C/T]GGTTTTGATTTGTAT	8925
rs139715278	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63666837	CTAAAAAGTTTAGTC[C/T]CTCAACATATGTGTT	8925
rs139741898	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63615692	ACATATTAGCAGATT[C/T]TGGCATACCCAGTCA	8925
rs139743206	snp	A/G	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63819948	TAAGTTTAAACGTGC[A/G]TTAAATAATACATGG	8925
rs139745033	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63784407	GTATTTGTGTATACT[A/G]TAATAGTTCATATAC	8925
rs139745343	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63794943	TGGTGGTGTGTACCT[A/G]TAGTCCCAGCTACTC	8925
rs139754041	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63702405	TCAAAATATTTAAAG[A/T]TTAGGGGCGATAATC	8925
rs139759139	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63724743	GGGGTACCAGATAAG[C/T]CTTCATGTTCAGTCT	8925
rs139808862	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63832317	TACGTACATTTATGC[A/C]TAAGACAGGCACCTA	8925
rs139809826	snp	A/G	0.0197687	0.0974348	intron-variant	HERC1	GRCh38.p7	15:63621826	TAGTTTTCGTGCCAC[A/G]GTTTTCAGCTCCATC	8925
rs139816941	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63698387	CTCACCATTGCACTA[C/T]AGCCTGGGCAACGAG	8925
rs139821091	snp	C/T	1.65993e-05	0.00288086	missense	HERC1	GRCh38.p7	15:63678154	CGGCTTTTCTTTAGC[C/T]TCTGACCTGACTCTT	8925
rs139827570	in-del	-/G	0.0287284	0.116357	intron-variant	HERC1	GRCh38.p7	15:63670176	GTTATGGAAAGAAAA[-/G]GTAACTGTCTAGTCA	8925
rs139830307	snp	C/T	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63664726	TGATAAAATTTGAAA[C/T]ACATCTTTATCCCTT	8925
rs139840287	snp	C/T	0.000994101	0.0222725	intron-variant	HERC1	GRCh38.p7	15:63638694	ACCATCATACAGTTA[C/T]CTTCATCTTTACTGA	8925
rs139874944	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63609403	GTGGACACAGAGACT[A/G]GGCCAGATAGAATGA	8925
rs139875402	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63793199	GCTGAGACCTACCAG[C/G]CTGAATTCCCAGGAG	8925
rs139886399	snp	C/T	0.02016	0.0983543	intron-variant	HERC1	GRCh38.p7	15:63780766	GGTTAGCTGTAAGAC[C/T]GAGCACAGCTACTAC	8925
rs139887212	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63719655	AAATGATGATGACTC[A/T]GAAAAAGGTAAGAGC	8925
rs139896454	snp	A/C	0.0119091	0.0762411	intron-variant	HERC1	GRCh38.p7	15:63653374	CTTGAACCCGGGAGG[A/C]GGGGACTACAGTGAG	8925
rs139898201	snp	C/T	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63750481	ACAAAATCAAAACAA[C/T]CAGCAATCTGAATGA	8925
rs139906239	snp	A/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63677529	AACAGAAATGATCAA[A/T]ATGCAAAAAGCCAAA	8925
rs139924560	snp	A/T	0.000366661	0.013535	intron-variant	HERC1	GRCh38.p7	15:63725252	TCCAACTGAGGTACA[A/T]ACAGGCATGTATTTT	8925
rs139924686	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63769187	CTTTGGGAGGCCTAT[A/G]CAGGTGGATCACCTG	8925
rs139929853	snp	A/T	0.0287284	0.116357	intron-variant	HERC1	GRCh38.p7	15:63650186	GACGGGCGGATCACC[A/T]GAGGTCAGGAATTCG	8925
rs139947542	snp	A/G	0.0205511	0.0992634	intron-variant	HERC1	GRCh38.p7	15:63791016	TAAAAAAGTTTTTCA[A/G]AGGGTTGACTGTATC	8925
rs139951886	snp	A/G	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63715869	GTGTAGTCAGTGGGT[A/G]AAATTTATAATTTTA	8925
rs139955147	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63832967	ATATTCTAAGTATTA[C/T]AGACATTTCTTAAAC	8925
rs139957266	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63766740	TGGAGTGCAATGGCA[C/T]GATCTCGGCTCACTA	8925
rs139958932	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63609747	TCCCTGTCCTCATGT[A/G]CATTCTGCCTCCTTT	8925
rs139977611	in-del	-/AC	0.0185938	0.0946107	intron-variant	HERC1	GRCh38.p7	15:63704119	AAAAGGAAAAAAAAT[-/AC]AGTCATTTATTTTAC	8925
rs139985026	snp	A/G	0.0341408	0.126114	intron-variant	HERC1	GRCh38.p7	15:63829410	CCTGGGTGACAGAGT[A/G]AGGCCCTGTCTCAAA	8925
rs140016531	snp	C/T	0.030278	0.119257	intron-variant	HERC1	GRCh38.p7	15:63823781	CTACTATTATTCCAT[C/T]ATTATTATTCCATTA	8925
rs140072434	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63649578	CTTTCAATTCAGTAA[C/G]TAATTAAAATTAAAA	8925
rs140084273	snp	C/T	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63818366	TGTGTACAAAAACCC[C/T]TTCCTGCCTGCCTAC	8925
rs140101758	snp	A/G	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63766574	ACAGAATGAGACTCC[A/G]TCTCAAAATAAAAAA	8925
rs140104439	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63709790	AAAAATCCTAGATTT[C/T]TAGTGGGTTTACTGG	8925
rs140105278	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63648300	TGATAATGCAACCAT[C/T]GCAAGTAAATTTCCA	8925
rs140136366	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63707175	TGCCTAAAGCCTTGA[A/C]GTAGTGCCTTATTTT	8925
rs140160746	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63733182	ACAAGTAACTAGCGT[-/A]ATATGCACTAGAAAA	8925
rs140163415	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63815701	TGGATATATTTTTTT[C/T]ACTCTGTTCAAATCC	8925
rs140169879	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63745687	CTTCAGTGCCTCTTT[C/T]AGTGATATGAAGTTA	8925
rs140177688	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63682463	AGTGGGAGGGGAAAG[A/G]GTTCAAAAACCCCTG	8925
rs140178900	snp	A/C	0.0119091	0.0762411	intron-variant	HERC1	GRCh38.p7	15:63660260	GGGAGGCCGTGGCTG[A/C]AGTAAGCTGAGATCA	8925
rs140195765	snp	A/G	0.0509478	0.151255	intron-variant	HERC1	GRCh38.p7	15:63811741	GTGAACCCAGAAGGT[A/G]GAGCTTGCAGTGAGC	8925
rs140222643	snp	C/T	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63799473	CCACTGCACTCTAGC[C/T]TGGGTGATAGAGCAA	8925
rs140236384	snp	C/T	0.0689305	0.172377	intron-variant	HERC1	GRCh38.p7	15:63722061	GTAGAGACAGGGTTT[C/T]GCCATGTTGGCCAGG	8925
rs140265304	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63791942	TCACTGATTTAATCA[A/C]CTGCTTTCCAGTGTA	8925
rs140268884	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63830761	TAAAATCCATCAACC[A/C]ATCATCTGATACAAC	8925
rs140285259	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63813651	GTGTGGGAAGAAGAG[A/G]AGAGGAAACTATCCA	8925
rs140301919	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63826262	TTGGTTTTTTGGCAC[C/T]GCTAAAATCTAATAG	8925
rs140304406	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63774471	GAATCCACAAAGCTA[A/T]AACTATAAACCTGAC	8925
rs140305651	snp	A/G	0.0115144	0.0749975	intron-variant	HERC1	GRCh38.p7	15:63716715	TTAAAATATCATGCT[A/G]TAAATTTATTCATAT	8925
rs140315209	snp	C/T	0.0252325	0.109451	intron-variant	HERC1	GRCh38.p7	15:63645159	AAGTAAAAATATTTC[C/T]GAATTGCAATCAATT	8925
rs140358223	snp	A/G/T	0.00915349	0.0671449	intron-variant	HERC1	GRCh38.p7	15:63824435	GCTACTTAGGAGGCC[A/G/T]AGGCAGGAGAATCAC	8925
rs140368706	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63770901	GTGTAAGAAACATGG[C/G]TTCTAGGCTGGGCAC	8925
rs140372880	snp	C/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63810592	ATAACCTTTTTTATA[C/T]TATGTAAGTTTCTTA	8925
rs140381066	snp	C/T	8.6494e-05	0.00657568	intron-variant	HERC1	GRCh38.p7	15:63699021	AACAGAATAAACATA[C/T]ATCAATGGCAATCAA	8925
rs140383419	snp	C/T	0.00597247	0.0543191	intron-variant	HERC1	GRCh38.p7	15:63684201	ACATGTTAAGCTTTC[C/T]AGAATAGTTGCAGTT	8925
rs140438625	in-del	-/AACC	0.437259	0.165632	intron-variant	HERC1	GRCh38.p7	15:63800883	GCTGGTTGCCAGAGA[-/AACC]AACCAAGTGATAAAA	8925
rs140439274	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63806395	TTGTAATCACCCTAC[C/G]CTCACCAACACAGAT	8925
rs140442034	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63824364	CAGTGAAACCCCATC[G/T]CTACTAAAAATACAA	8925
rs140450623	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63680411	ATGTTTTAAGAACCA[C/G]AAAGTATTAGAGAGA	8925
rs140508968	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63777036	AATATTGCAGGGAAG[A/G]TGTCTCTCAAGCAAG	8925
rs140509325	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63808286	TTTTAGAACATCAAC[A/G]TACTTTTTCTTTCCT	8925
rs140516202	snp	A/G	0.0182019	0.0936463	intron-variant	HERC1	GRCh38.p7	15:63739229	TTTAGATGGAGACTC[A/G]TTCTGTTGCCCAGGC	8925
rs140524377	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63640915	AGAGAATCCTGGTAG[C/T]CATCAAAGGAAAAGC	8925
rs140530517	snp	C/T	0.0107246	0.0724382	intron-variant	HERC1	GRCh38.p7	15:63618836	TTTGTGATTTTTGCA[C/T]ATTGATTTTGTATCC	8925
rs140556028	snp	A/C	0.000454614	0.0150699	intron-variant	HERC1	GRCh38.p7	15:63652582	AATAATTTTCTATTC[A/C]AATGATTTTATTATT	8925
rs140568625	in-del	-/A	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63610934	GGGTTTGAGGGCTGT[-/A]ACCCAGTGTTCAGGA	8925
rs140575071	snp	A/C	0.0360663	0.129354	intron-variant	HERC1	GRCh38.p7	15:63772605	CAGAAAGTATTAAGA[A/C]TCAGAAAACAAAGTT	8925
rs140600378	snp	C/T	0.0268082	0.112764	intron-variant	HERC1	GRCh38.p7	15:63664000	TTTACATGCCCAGAA[C/T]GTAATCCTAGAATTT	8925
rs140632966	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63803702	TTCCTCCTAACCACT[C/G]TTTCAAGATTATTAA	8925
rs140649190	snp	A/G	0.0588605	0.161139	intron-variant	HERC1	GRCh38.p7	15:63707758	ACAAGGTGAAACCCC[A/G]TCTCCACTAAAAATA	8925
rs140651284	snp	A/G	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63633665	CAGTTTAGCTGGATT[A/G]ATAGCTTATTTAAAA	8925
rs140668677	snp	A/T	0.00914312	0.0669923	intron-variant	HERC1	GRCh38.p7	15:63644143	TACTCCTTCCCTCCC[A/T]CTCCACCCTTTCTCC	8925
rs140703182	snp	A/G	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63738215	CAGAGATATTCAATA[A/G]AATAATTAAATAATA	8925
rs140716374	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63685054	TTTGTCTTGAAAGCT[G/T]CTGTGAGCACTTTAA	8925
rs140724885	snp	C/G	0	0	intron-variant	HERC1	GRCh38.p7	15:63756309	AAACTGTAAAGCAGA[C/G]ATACAAAAGATTAAG	8925
rs140737621	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63735165	AATCTCTGCTTTCAT[A/G]AGCCTACAGTCTAAT	8925
rs140742435	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63661167	ATGTTATAGGCTAAC[A/G]TAATAAAAACTGCTG	8925
rs140759316	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63796488	TCCATCATCGATCAT[G/T]CCGGGGTGTAGACTG	8925
rs140761358	snp	C/T	0.02016	0.0983543	intron-variant	HERC1	GRCh38.p7	15:63725923	AATGCTTTTTAAGGC[C/T]TGAATTCAGAATTGT	8925
rs140788466	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63825082	GGGAGGCCGAGGCAG[A/G]GAGATCACTTGAGGC	8925
rs140789375	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63751981	TCATAAAAAAAGAAG[C/T]ACATGATGCTCAAGG	8925
rs140792783	snp	C/T	0.00398564	0.0444627	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834382	GGCCGGCGGCAGGGC[C/T]AGGGCCTCACCCCTT	8925
rs140804461	snp	C/G/T	0.00716266	0.059414	intron-variant	HERC1	GRCh38.p7	15:63759050	TTTCCTTTAATAGGG[C/G/T]ATTTAGAGTCTATTT	8925
rs140819055	in-del	-/ACACAT/ACAT			intron-variant	HERC1	GRCh38.p7	15:63718121	CACACACACACACAC[-/ACACAT/ACAT]ACAACCCCCTCCTTG	8925
rs140832415	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63752791	CAGGTTAGAAAACCT[A/G]GTTCCTTCTCAGATA	8925
rs140836125	snp	G/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63622285	TATTATCATTGATTT[G/T]GTCTCAATAAATACC	8925
rs140836204	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63679921	TAATATATCGTAAAG[C/T]CAATTTCTGAAAGTA	8925
rs140853434	snp	A/C	0.0655868	0.168795	intron-variant	HERC1	GRCh38.p7	15:63793315	TAAAGAAGCTGGCCC[A/C]AACCCACCAAAACCA	8925
rs140854301	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63821225	CCAGGAGTTTGAGAC[C/T]AGCCTAGGCAACAGA	8925
rs140866149	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63793629	TGCCTATGGAGCAGA[C/T]ATTCTTTATTCCTTT	8925
rs140930579	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63786917	TCAACTCAATAAATT[-/A]TTATTTTTTTTTTTT	8925
rs140940738	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63710264	CAGCAGGTAGGTGTT[C/T]TGTTGTTGTTATGTG	8925
rs140947797	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63610075	ACTATTTTCTAAACA[A/C]TTTGTAATAATAGTA	8925
rs140952144	in-del	-/A	0.0252325	0.109451	intron-variant	HERC1	GRCh38.p7	15:63759472	TGAATCCATACTCAT[-/A]ATAAGTATCATGCTT	8925
rs141007352	snp	A/G	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63779308	TCCAAGAAATAGCCT[A/G]GAAAAACTATTATAT	8925
rs141008934	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63719059	CTGTTCCAAGCGCTG[A/T]GGATATAGCAGTGAA	8925
rs141014376	snp	C/T	0.0256215	0.110247	intron-variant	HERC1	GRCh38.p7	15:63646066	ATGCACCCCTTACAT[C/T]CCAATAGCAAACACT	8925
rs141069702	snp	C/T	0.0566069	0.158427	intron-variant	HERC1	GRCh38.p7	15:63714737	TATCTTTAGTAGAGA[C/T]GGGGTTTCACCATGT	8925
rs141080435	snp	C/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63731215	TCCTGTAAATAATCA[C/T]GTGCTGAATATCTTT	8925
rs141087130	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63721339	GACCAGCCATGGCCA[A/G]CATGGCATAAACCCC	8925
rs141097490	snp	A/G	0.00426512	0.0459822	intron-variant	HERC1	GRCh38.p7	15:63648048	ATCCCATAAAATTAC[A/G]TTTTTTAAAGATGCA	8925
rs141141747	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63693519	AAAGTGTTGGCATTA[C/T]GGTTGTGAGCCACTG	8925
rs141147660	snp	C/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63749098	TTTTTTAAATCAGCA[C/T]GTAGAGATGAGAGAG	8925
rs141150955	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63763107	ACAATAGCCATGGCC[C/T]CCTGGTGTCCCACCT	8925
rs141155187	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63717724	AAAAATACAAAAAAT[C/T]AGCAGGGCGTGGTGG	8925
rs141163148	snp	A/C	0.00953873	0.0683987	intron-variant	HERC1	GRCh38.p7	15:63645384	AGAATAGCAACTGGC[A/C]ATAAACTCTTTAAGA	8925
rs141167444	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63622648	TGTTTCCTCATCTTT[C/G]ACAAGAGGATAACAA	8925
rs141213085	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63810766	TTACAAAGGGGAAAA[A/T]AGTGTACATTTGCAA	8925
rs141214703	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63807536	GGCCTTGGGAACATG[A/C]CAATACTCTGCTGCT	8925
rs141220405	snp	A/G	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63738634	AACAGCAGCAATGTG[A/G]TTACTGCAAATAGAT	8925
rs141225310	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63643186	ATTCAGCAACGTCCA[A/G]TCACATACCTACTAC	8925
rs141232437	snp	C/G	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63628189	GGAGGTCAGGAATTT[C/G]AGACCAGCCTGGCCA	8925
rs141271203	snp	A/C	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63730128	TTAGATGGTAAAATT[A/C]ATCAAGCTACTTCTA	8925
rs141274060	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63771494	GGAGTGCAATGGTGC[C/G]ATCTCAGCTCACTGC	8925
rs141277059	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63804980	TGTGTAGAACTCTCA[C/T]ACACTGCTGGTAGAA	8925
rs141309106	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63697786	TTAAGGCAATACCTG[A/C]CAGGTTTCTGCAATG	8925
rs141331867	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63791453	ATCAATGCAGCAAGA[C/T]TTGCCAAACATAAGG	8925
rs141332010	snp	G/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63742110	TATTAAGTCTTGCAA[G/T]CCATAAACATGAGGT	8925
rs141342240	snp	A/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	HERC1	GRCh38.p7	15:63668909	ACTTGGACAACAGTA[A/T]CAACCAATTTGAGCC	8925
rs141348087	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63614974	CAGGTTGGTGACCTG[A/G]AGGTAAGCTTGTGTG	8925
rs141363085	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63805813	CCATGTATAGTGGTA[C/T]GCTTCTGTGGTCCTA	8925
rs141379412	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63709337	AAAATGGGTTTTTTT[G/T]TAGTCTTTTTAAAAA	8925
rs141384472	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63637940	TGGGCTAGAAAGAAG[C/T]AGAAACTCGTACATA	8925
rs141395578	snp	A/G	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63787542	ACTGAAAGAAGAGAG[A/G]ACCAATGGTGGGCAA	8925
rs141404541	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63703811	CTACTTGAGAGGCTC[A/C]GATGGGAGGGTCACT	8925
rs141414233	snp	A/C/G	0.0104743	0.0716078	intron-variant	HERC1	GRCh38.p7	15:63686355	TATTAGATTTTCTAC[A/C/G]TACCTTCCACTGATA	8925
rs141415966	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63617461	ATGAATAGTGCCGCA[A/G]TAAACATACGTGTGC	8925
rs141417922	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63627507	GGCGAAACACCATCT[C/T]TACTAAAAATATTAA	8925
rs141445385	snp	C/T	0.00597247	0.0543191	intron-variant	HERC1	GRCh38.p7	15:63797980	GCCCCATAATATCAC[C/T]CCCTGGAAAAATTAA	8925
rs141447564	snp	A/G	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63727422	AGATAGGCCCTCAAG[A/G]TCATCTTTCCAACTC	8925
rs141450593	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63816097	ACAGCCAAACCATAT[A/C]CCTAACATTTCCCAA	8925
rs141451793	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63701703	TTAAGAACAGGAAAC[A/G]CACTATGTGGAAGCA	8925
rs141467601	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63700901	AAAGAATAAAGTAGA[G/T]GCTAATGTAAAAAAT	8925
rs141475889	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835245	AAAATATATGTAAAG[C/T]TCACATACGGCACAT	8925
rs141517117	snp	C/T	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63754973	TCAGGATCATGATGG[C/T]ATTGCTTTTATCCCA	8925
rs141523202	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63682274	GTTTGCTACCCCAGA[C/T]GCTCTTGGCCTTGCT	8925
rs141533214	snp	C/G	0.00018296	0.00956276	intron-variant	HERC1	GRCh38.p7	15:63623702	GACTAGATAACTCAG[C/G]AGGGGACACTGCAGG	8925
rs141538304	snp	A/C	0.00636936	0.0560724	intron-variant	HERC1	GRCh38.p7	15:63676247	ATCCTTTCTGAAACA[A/C]GGCAAAGAATGAGAG	8925
rs141550985	snp	A/G	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63794128	GGGGAGGCATGAATA[A/G]TCCACCCCTTGTTTA	8925
rs141571536	snp	A/G	0.0123036	0.0774623	intron-variant	HERC1	GRCh38.p7	15:63612802	TCAAGTCCAATTTAG[A/G]AGCCTGCCTTCCCTC	8925
rs141582502	in-del	-/A	0.0566069	0.158427	intron-variant	HERC1	GRCh38.p7	15:63705508	ATATACATGAAAATG[-/A]AAAAAATTATGTGTG	8925
rs141599959	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63718294	GCCCAATCAGCACAA[A/C]GAGAGGAATAATCAT	8925
rs141601975	snp	A/G	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63671139	ACTCAGGAGGCTGAG[A/G]TTACGGTGAGCCCAG	8925
rs141624946	snp	G/T	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63788379	AATCAGTAATGAGAT[G/T]TAAAGAAACTATAAT	8925
rs141627446	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63667892	TCCTAGCCTACTCAA[C/T]GGGAATATGACTATA	8925
rs141642559	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63630180	AGCTTACTACATGCC[A/G]GGCACTTAACAGTGT	8925
rs141663885	snp	C/T	0.0107246	0.0724382	intron-variant	HERC1	GRCh38.p7	15:63788843	TCGCGCCATTGCACT[C/T]CAGCCTGGGTAACAG	8925
rs141670849	snp	A/C	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63714241	TATATTAGTTACAAC[A/C]AAAAATTCCCTTTCC	8925
rs141681855	snp	G/T	0.02016	0.0983543	intron-variant	HERC1	GRCh38.p7	15:63787154	GTCTCAATAAATTAT[G/T]ATTATCATATTATTA	8925
rs141690240	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63711241	GAGGCAGGAGGATTG[C/T]TTGAGCTCAGGAGTT	8925
rs141700842	snp	A/G	0.00676609	0.0577691	intron-variant	HERC1	GRCh38.p7	15:63676743	CCTGGGCGACAGAGC[A/G]AGATTCCGTCTCAAA	8925
rs141731116	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63798721	ACCTTATTTTAATTC[C/T]CTGCCATACAACCTA	8925
rs141750184	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63726493	ATGGCACAAATTCAA[A/G]AAATAGGAATAAACA	8925
rs141764656	snp	C/T	0.000717411	0.0189259	intron-variant	HERC1	GRCh38.p7	15:63732892	TCCCTACCCCTTTAT[C/T]CTTTTTTTACTACAA	8925
rs141804029	snp	C/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63743531	GCCTCCAAAAGTGCT[C/G]GGATTACAGGCGTGA	8925
rs141805954	snp	A/G	0.00398564	0.0444627	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834667	CACGTGAAACCCCAT[A/G]AGGGGAAGGACACAG	8925
rs141808300	snp	A/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	HERC1	GRCh38.p7	15:63669357	TATTTCTCTCCGAAA[A/T]GGCCATAATTCAATC	8925
rs141818232	snp	C/T	0.0103295	0.0711199	intron-variant	HERC1	GRCh38.p7	15:63767470	TTTGGGAGGCCAAGG[C/T]GGGTGGATCATCTGA	8925
rs141838203	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63724300	TTAAAGACCCCTTGA[A/C]AAACCATGATTTTAC	8925
rs141841722	snp	C/T	0.0633504	0.166319	intron-variant	HERC1	GRCh38.p7	15:63649345	TGACAGAGCGAGACT[C/T]CTTCTCAAAACAAAA	8925
rs141870333	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63765809	TGGGCACCTGCCACC[A/G]GGACTTCCTGAGGCT	8925
rs141875254	in-del	-/AAAAG			intron-variant	HERC1	GRCh38.p7	15:63652038	GAGACTCAGTCTCAA[-/AAAAG]AAAAAAACAAAACAA	8925
rs141879319	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63663282	AGTTCTTAACTGCCA[C/T]ACATGTAGGTGAGAA	8925
rs141883645	in-del	-/ATTCTTA	0.0652144	0.168387	intron-variant	HERC1	GRCh38.p7	15:63768025	CCATTAATAATCATT[-/ATTCTTA]ATTATTCTCTTCAGC	8925
rs141884474	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63615384	GAAGCTGAGGCAGGT[A/G]GATCACTTGAGGCCA	8925
rs141911299	snp	A/G	0.0119091	0.0762411	intron-variant	HERC1	GRCh38.p7	15:63704900	CCCACCACCACGCCC[A/G]GCTAATTTTTTGTAT	8925
rs141933666	snp	A/C	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63815005	AAATGAGTTCCAAAG[A/C]ATTTCTAAATCTGAA	8925
rs141939707	snp	C/T	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63792288	ATTTGAATAAAATAA[C/T]CTCCGAAGTCCTTTC	8925
rs141945022	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63718969	TAATTTTTATAGCTT[C/T]AGTCATCCAACACCT	8925
rs141964439	snp	A/T	0.00597247	0.0543191	intron-variant	HERC1	GRCh38.p7	15:63657579	TCTATGGCTTGCTTT[A/T]TTACTTTCTTACTTT	8925
rs141975386	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63827343	AGGAGGATCGCTTAA[A/G]CCCAGGGGATTAAGG	8925
rs141979703	in-del	-/AT			intron-variant	HERC1	GRCh38.p7	15:63829585	TATATATATATATAT[-/AT]ATATATATAATATAC	8925
rs142044246	snp	C/G	0.0260105	0.111035	intron-variant	HERC1	GRCh38.p7	15:63651907	CGGGCATGGTGGCAG[C/G]CACCTGTAGTCCCAG	8925
rs142055977	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63688619	AATCCAACACTTAGA[C/T]TGAATAGAAGAAGAA	8925
rs142063728	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63768798	GGTCTCATCCTGAGA[C/T]GGGAATGATGCCCAC	8925
rs142075179	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63697417	CTCATTACACTATAT[C/T]GACATGACTTAATAC	8925
rs142093103	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63703220	TCCTACATATTCACT[G/T]TCTCAGACCAAGGGC	8925
rs142098478	snp	C/T	0.100588	0.200439	intron-variant	HERC1	GRCh38.p7	15:63767161	GCACGCCACCATGCT[C/T]AGCTAATTTTTTTGT	8925
rs142108980	snp	C/T	1.70012e-05	0.00291553	intron-variant	HERC1	GRCh38.p7	15:63694569	AAGACAAAGAGACAG[C/T]TAAGAATCTTCCTTT	8925
rs142124229	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63821430	GCATGGTGGCATGCA[C/T]CTGTAGTCCCAGCTA	8925
rs142126832	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63740192	GCAGATTACAGGTGT[A/G]GGCCACTGCATCCAG	8925
rs142130100	snp	A/C	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63784106	ATGCTCATACTCATA[A/C]AAATGAGCAAATTTC	8925
rs142156372	snp	A/T	0.0298908	0.118541	intron-variant	HERC1	GRCh38.p7	15:63757510	GATCTCAAACGATCC[A/T]CCCGCCTTGGCCTCC	8925
rs142165873	snp	C/T	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63782966	GCAGCAATCTCATGA[C/T]AAAATTTTAACGGAT	8925
rs142166486	snp	C/T	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63653429	GTCTGGGTGAGACTC[C/T]GTTAAAAAAAAACTG	8925
rs142168062	snp	A/C	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63820685	AACAGAGACGTTATC[A/C]TTTTTTTTTTGCTTT	8925
rs142172063	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63708715	TTAAAAAGCATTTCA[C/T]TTACGAACAATTCAG	8925
rs142191661	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63819593	GTTCTCTTCTAACAT[C/T]TATTCCTCTCCTTGG	8925
rs142213994	in-del	-/GAC			intron-variant	HERC1	GRCh38.p7	15:63787983	AAAAAAAAAAAAAAA[-/GAC]AAAACAAAACAAAAA	8925
rs142218127	in-del	-/T			frameshift-variant	HERC1	GRCh38.p7	15:63652517	CCAAAAGACCTTTTT[-/T]ATTACACCAAACACA	8925
rs142231491	snp	C/G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63817669	GCAGTCAGCCAAGTT[C/G/T]GCGCCACTACACTCC	8925
rs142272241	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63824368	GAAACCCCATCTCTA[C/T]TAAAAATACAAAAAA	8925
rs142291149	snp	C/T	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63631740	GAGACGGCGTTTCGC[C/T]ATGTTGGCCAGGCTG	8925
rs142352147	snp	A/C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63711960	AAAGTTCCTCAAGTA[A/C/G]AAGCAATCTTCTAGA	8925
rs142352530	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63639873	TAAAGCACTAACAAA[A/G]TACCTATGGACAAAA	8925
rs142362238	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63642749	ACTGTCACCAAAGTA[C/T]GGGGTGTAGTAGAAA	8925
rs142427069	snp	C/T	0.0232847	0.105357	intron-variant	HERC1	GRCh38.p7	15:63803304	TAAATAGCCCAAGGT[C/T]ACAACTGCCAGTAAT	8925
rs142427828	snp	A/G	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63638297	ATGACTTTCTTTAAT[A/G]ATTCCTCATAATAGA	8925
rs142434922	in-del	-/A	0.0225045	0.103662	intron-variant	HERC1	GRCh38.p7	15:63798096	CTCACTAAAGCACTT[-/A]TTTTAGAGAAGTGTG	8925
rs142468926	snp	C/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63746051	CTCTAATCTACATTA[C/G]TTCCTTTTTTCTACT	8925
rs142470603	snp	C/T	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63747416	AGTGAACTGAGATCA[C/T]GCCACTGCACTCTAG	8925
rs142471563	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63818975	AAATTTATGTAAAAC[A/G]CCTAGGCTTTTGGTA	8925
rs142480754	snp	C/T	1.66043e-05	0.00288129	synonymous-codon	HERC1	GRCh38.p7	15:63674409	TTTATAGATCATGGC[C/T]TGCGCTCGTTCCAGA	8925
rs142483762	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63750019	AAATAAAAATAACTG[A/G]TCATAGAAAAAACAG	8925
rs142503479	snp	C/T	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63725902	AAATGACATTCAAGA[C/T]TGTTTAATGCTTTTT	8925
rs142531455	snp	C/G	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63803280	AGGGAAGTGGAGGTA[C/G]AGAGAGGCTAAATAG	8925
rs142532425	snp	G/T	0.0138799	0.0821421	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834164	AGGTGCTGGGGACAC[G/T]TTGCTACCGCGCGGC	8925
rs142536163	in-del	-/AT	0.0248432	0.108648	intron-variant	HERC1	GRCh38.p7	15:63737350	ACAAAACACTTCCAG[-/AT]ATATATATATATCTT	8925
rs142537034	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63764714	CCAGGTATGTCAGGT[C/G]ACCATCAAGTGATGG	8925
rs142537231	snp	C/G	0.031825	0.122064	intron-variant	HERC1	GRCh38.p7	15:63766960	TGGGATTACAGGCGT[C/G]AGCCACCATGCCCAG	8925
rs142543106	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63690145	TCACTCCAGGCTGGG[C/T]GACAGAGCGAGACTC	8925
rs142543858	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63805215	GGTACATCATAATAT[A/G]TGCATACAATGGCAT	8925
rs142544633	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63664346	TGATATCCAAATAGC[A/T]GTTCTGTTAATGTGG	8925
rs142551158	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63766643	TACTTAGAATTTTTT[A/G]AGTTTCGTAATACAT	8925
rs142553976	snp	A/T	0.0325976	0.123435	intron-variant	HERC1	GRCh38.p7	15:63635028	AAAGACCAATGCTTT[A/T]AAAAATTTTTTTTTT	8925
rs142560537	snp	A/G	0.00636936	0.0560724	intron-variant	HERC1	GRCh38.p7	15:63616894	AGCCACATGTGGACC[A/G]TAGTTATTGTTTCAC	8925
rs142571550	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63780475	ACCTGTAATCCCAGT[A/G]CTTTGGGAGGCCGAG	8925
rs142578274	snp	G/T	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63706701	AAACAGCTTCTTAAT[G/T]TATTTACTATGCTCT	8925
rs142594434	snp	C/T	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63800355	TCTCTTCTATAGACG[C/T]CTGAGATCCTTAACT	8925
rs142606357	snp	C/T	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63793369	GGTAGTCCATACTGC[C/T]CATTATACACTAATT	8925
rs142611494	snp	C/T	0.0205511	0.0992634	intron-variant	HERC1	GRCh38.p7	15:63721315	GATCACCTGAGGTCA[C/T]GAGTTCGAGACCAGC	8925
rs142617300	snp	A/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63801676	TCCAGGTAGTCCATT[A/T]TGCATATTGAATATA	8925
rs142640461	in-del	-/TT	0.0287284	0.116357	intron-variant	HERC1	GRCh38.p7	15:63629935	GAATACATCAACCTC[-/TT]GAGTCTCTTATCAGT	8925
rs142650802	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63779425	TTAAAACAAAATAGC[A/C]CAGCCACAGCTTTTA	8925
rs142656764	snp	A/T	0.00874735	0.0655527	intron-variant	HERC1	GRCh38.p7	15:63659089	TATTTTGTATTCCCT[A/T]TACCAAAAATTTACC	8925
rs142673524	in-del	-/AC	0.0603597	0.1629	intron-variant	HERC1	GRCh38.p7	15:63660874	TGTACACAAATACAA[-/AC]ACACACACACACACG	8925
rs142692222	snp	C/T	0.0232847	0.105357	intron-variant	HERC1	GRCh38.p7	15:63779938	AGAATCGCTCGAACC[C/T]GGGAGGTGGAGGTTG	8925
rs142695284	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63829472	TGTGCACATATATGT[A/T]TATATAAATATATAT	8925
rs142747126	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63625142	CACACACACACGCAC[A/G]CACACACAATAGCTA	8925
rs142753603	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63609615	TCCTTCATACCCATC[C/T]ACCAAGAGGGTGCAG	8925
rs142768471	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63695911	CTGGATTAATAAAAC[C/T]GAGCCAGCAAATAAT	8925
rs142776598	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63819921	CTTATCTGCAAATAA[A/G]GTTTTACCCCATAAG	8925
rs142779987	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63612083	GTCCCAGCTACTGCG[A/G]AGGCTGAGGCAGGAG	8925
rs142780610	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63751526	GCAGCGTTCCTTCGG[C/T]TGAGCACCAGATGAG	8925
rs142789067	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63660427	CACCATCTCCTGAAA[-/A]CTTAACCAAACTGCA	8925
rs142829699	snp	A/G	0.0103295	0.0711199	intron-variant	HERC1	GRCh38.p7	15:63691276	TTCAAGACCAGCCTG[A/G]CCAACATGGTGAAAC	8925
rs142829886	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63735871	CAGGACAAATCTTTA[A/C]TGACTTTCTCAGAGT	8925
rs142863301	snp	A/G	1.73105e-05	0.00294193	intron-variant	HERC1	GRCh38.p7	15:63665895	ATAACACATGGAACA[A/G]AAGTACAGAAACTGG	8925
rs142876852	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63801191	TCATTTATAATAAAC[C/T]AGTCATTGTAAATAG	8925
rs142884921	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63732414	CAGCAATAGTGACAA[A/T]AGCTATAACATTATT	8925
rs142886526	snp	A/G	0.00953873	0.0683987	intron-variant	HERC1	GRCh38.p7	15:63644853	TTAAGCTAATTCAGG[A/G]TGACAATTACTTATA	8925
rs142921393	snp	A/C/T	0.00636936	0.0560724	intron-variant	HERC1	GRCh38.p7	15:63736691	TCGGCTCACGGCAAC[A/C/T]TCCACCTCTGGGGTT	8925
rs142923015	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63783428	AAAAAAGTATTTTTT[A/G]ATTAAGGTACATACA	8925
rs142929421	snp	C/T	0.0252325	0.109451	intron-variant	HERC1	GRCh38.p7	15:63664147	TCTTACCACTGATGC[C/T]AAACATTAAACATGC	8925
rs142936354	in-del	-/TGTGTGTGTGTGTGTGTGTGTGTGTGTG			intron-variant	HERC1	GRCh38.p7	15:63744111	TTCTCCCAAACAGAC[-/TGTGTGTGTGTGTGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT	8925
rs142943641	snp	C/G	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63744824	AATCAGGGATCCCAA[C/G]AGTGTATTTGGTACT	8925
rs142980230	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63807121	ATTATAACACTACCC[C/T]ACTTTATAAATTTGC	8925
rs142983358	snp	C/T	1.70953e-05	0.00292359	intron-variant	HERC1	GRCh38.p7	15:63616391	TCTGTGCATATAGGA[C/T]GTCAACACCAGTAGA	8925
rs142984371	snp	C/T	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63828176	AATATAAGAGAACAC[C/T]CACATATATTTTCAT	8925
rs142986860	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63761212	CTATCAAAAAGAATA[A/G]ACACTGACACAGAGA	8925
rs143013371	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63791790	AATTTTTTCCTTACT[A/G]AGAATAAAGAAGTTG	8925
rs143048871	snp	C/T	0.0287284	0.116357	intron-variant	HERC1	GRCh38.p7	15:63619684	TCAGAGCCTGTTTGG[C/T]CTATTCAGAGATTCA	8925
rs143087202	snp	C/T	0.0107246	0.0724382	intron-variant	HERC1	GRCh38.p7	15:63681766	CCTTGGGTTCTGAAT[C/T]TCTAATGGGGTTCTC	8925
rs143095483	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63659236	GGTATCATGAAAGAC[-/A]AAAAAAAAATCAAAA	8925
rs143097937	snp	C/T	0.00386004	0.0437621	utr-variant-3-prime, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609044	CAGAAGTGAGCATTA[C/T]TGAGGGAGAGAAGGG	8925
rs143131927	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63830242	AAAGTTAAAATACCA[C/T]TAGCAAAAAGACATG	8925
rs143141943	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63763202	TGGTGTTGGGTCTGA[C/T]CACCCCAACACTAAT	8925
rs143161489	snp	C/G/T	0.0154538	0.0865337	intron-variant	HERC1	GRCh38.p7	15:63636942	TGAAAAGAACCTGAG[C/G/T]TTCTAGGAACTTGTT	8925
rs143194649	snp	C/T	0.00636936	0.0560724	intron-variant	HERC1	GRCh38.p7	15:63675274	AAACACAGAGAAAAA[C/T]GAGTCTATTATGAGA	8925
rs143199500	snp	C/T	8.58406e-05	0.0065508	intron-variant	HERC1	GRCh38.p7	15:63648054	TAAAATTACGTTTTT[C/T]AAAGATGCATTTACC	8925
rs143229625	in-del	-/CA	0.0426437	0.139654	intron-variant	HERC1	GRCh38.p7	15:63747683	GCACACACGCGCGCG[-/CA]CACACACACACAAAG	8925
rs143250798	snp	A/T	0.00557542	0.0525036	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835092	GTGCTTCACTGTCAG[A/T]CACTGGTGGGAATTC	8925
rs143258169	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63768496	AACAACAAATACTTG[A/G]TTGCAACCTCTCCAA	8925
rs143260232	snp	C/G	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63738683	GAAATAAGAAAAGAG[C/G]AACACAAATAGCTGT	8925
rs143266233	snp	C/T	0.0244538	0.107838	intron-variant	HERC1	GRCh38.p7	15:63665617	TTTATATCACTTGTA[C/T]GAGATAAAATTATTT	8925
rs143267946	snp	A/C	0.177503	0.239258	intron-variant	HERC1	GRCh38.p7	15:63652040	GACTCAGTCTCAAAA[A/C]AGAAAAAAACAAAAC	8925
rs143268967	in-del	-/TGAAAG	0.0020135	0.0316653	intron-variant	HERC1	GRCh38.p7	15:63729695	TGAAGTGCTTGAAAC[-/TGAAAG]TAACAACCTACCATA	8925
rs143278098	snp	C/T	0.0582896	0.160459	intron-variant	HERC1	GRCh38.p7	15:63723170	TTACTCCCTTTATCT[C/T]CTTTATCTTACCTTT	8925
rs143293711	snp	G/T	0.00716266	0.059414	intron-variant	HERC1	GRCh38.p7	15:63782851	ACCCCTACGGATGAC[G/T]TTGAGAGGTTCAAGA	8925
rs143331314	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63722798	TTAAACTTTACCATG[C/G]GCAAGTATGTACACA	8925
rs143331823	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63831815	AATTGAGATTTTCAA[A/G]AGATGTTTATATTAA	8925
rs143334825	snp	C/T	0.00111631	0.0235989	intron-variant	HERC1	GRCh38.p7	15:63694582	AGTTAAGAATCTTCC[C/T]TTCAGTAAACAAAGC	8925
rs143342111	snp	C/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63765598	TCTCCCACAACTCCT[C/T]ATTGTAACCCACACA	8925
rs143342478	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63719280	GATAAGGTTACATTT[C/G]AGCAGAGATCTAAAT	8925
rs143353864	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63646182	CACATCTTCTAACTC[C/G]TGGTTTCATGCATTT	8925
rs143359892	snp	C/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63831094	GTTGTGTAGACCTTT[C/G]TTGTTGTTTGTTTTG	8925
rs143366834	snp	C/T	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63734991	AAGCATGCAAGTCCT[C/T]CTTCAGATGTCTTTA	8925
rs143369302	snp	A/C	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63728066	CCGTACCAACAAATT[A/C]AAAGGATTAAAACTG	8925
rs143397892	snp	A/G	0.000306572	0.0123771	intron-variant	HERC1	GRCh38.p7	15:63622804	TAATGAACACTTGCT[A/G]ACTGCCATACCTGTC	8925
rs143406089	snp	C/T	0.0130921	0.0798413	intron-variant	HERC1	GRCh38.p7	15:63810350	AGCCATAAAAAGAAA[C/T]GAAATTTTGATATAT	8925
rs143429687	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63611264	CAGACTGTGGAAGTG[C/T]TTAAGGCAGCTAAGG	8925
rs143430984	snp	G/T	0.02016	0.0983543	intron-variant	HERC1	GRCh38.p7	15:63795943	CCTTTAAATAAGGAA[G/T]AGGAACAGGCTACGA	8925
rs143435104	snp	C/G	1.65737e-05	0.00287864	missense	HERC1	GRCh38.p7	15:63725361	AATATGCAGTGTCCT[C/G]TTCCTCTGGAGACAC	8925
rs143442746	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63651478	CATATAGACTAGAGT[A/G]TATAACTGATTCTTC	8925
rs143502886	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63718377	AGTTTCTTAGAACCA[A/G]TATCACACTTGGTAA	8925
rs143508709	snp	C/T	0.00312795	0.0394232	missense	HERC1	GRCh38.p7	15:63645525	CCTTTCCCTGGAAGG[C/T]GGCACCAAGCAATGC	8925
rs143571739	snp	A/G	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63649097	CGGTGGCTCACGCCT[A/G]TAATCCCAGGACTTT	8925
rs143578318	snp	C/T	0.00478085	0.0486577	intron-variant, downstream-variant-500B	HERC1	GRCh38.p7	15:63669262	TTGCAGCTAAAGCAG[C/T]ACTTAAAGGGAAACT	8925
rs143600242	snp	A/C	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63809989	GCCAGGAAACAATCT[A/C]AAGTCCACAAATAAT	8925
rs143611400	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63711606	ATTCTTTATGTAGCA[C/T]TTTATACTTTTTCAA	8925
rs143632694	snp	A/T	0.0252325	0.109451	intron-variant	HERC1	GRCh38.p7	15:63663571	AGACATCCTCCTGTC[A/T]CAGCCTCTGAGTAGC	8925
rs143640075	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63765756	GATATATTATGTCGC[A/C]CTAAAATGTATAAAA	8925
rs143696558	snp	C/G	0.00835141	0.0640778	intron-variant	HERC1	GRCh38.p7	15:63705316	ATGCATCCACGCCTA[C/G]CTTTTTTTTTTCTTT	8925
rs143710444	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63813109	AAGAAGATTTTCAAA[A/G]TAAGACCTTCATAAA	8925
rs143717447	snp	C/T	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63741678	TTTTTTTGTATATGA[C/T]GTAAGGGGCCAACTT	8925
rs143746677	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63826285	TCTAATAGGATTGCC[C/T]TAACCCAGAACTTTA	8925
rs143749414	snp	A/G	0.0298908	0.118541	intron-variant	HERC1	GRCh38.p7	15:63760009	ATTGCTCATCTACAG[A/G]TCTATCACAGCCAGT	8925
rs143758889	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63656474	AAAATGTAAGCTGCA[C/T]TATCATTAGCCATAC	8925
rs143763238	snp	A/G	0.0663309	0.169604	intron-variant	HERC1	GRCh38.p7	15:63702895	GGGATCACGAGGTCA[A/G]GAGTTCAAGACCAGC	8925
rs143786459	snp	G/T	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63629161	CACCATCTTGGCCAG[G/T]CTGATCTTGAACTCC	8925
rs143789226	snp	A/G	0.0193772	0.0965046	intron-variant	HERC1	GRCh38.p7	15:63771680	TCAGGTGATCTGCCC[A/G]CCTCGGCCTCCCAAA	8925
rs143792996	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63664766	AATTATGCATATAAC[A/C]TTTCCTGTGACCTGA	8925
rs143817982	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63794293	TGAATTCTTTCTTGC[A/G]TGAGATCCAAGAACC	8925
rs143849175	snp	C/T	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63781136	CACTAATAAAACTGT[C/T]ACAAACAGTTTTATT	8925
rs143857583	snp	G/T	0.00795532	0.062565	intron-variant	HERC1	GRCh38.p7	15:63707325	TAAACCTTCTGGTAG[G/T]ATTTGAAAAGATTTT	8925
rs143884407	snp	C/G	0.0154538	0.0865337	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835800	TTGGCCTCCCAAAGT[C/G]CTGGGATTACAGGGG	8925
rs143895106	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63740121	TCACCATTTGGCCAG[A/G]CTGGTCTCAAACTCC	8925
rs143905395	snp	C/T	0.000119337	0.00772361	intron-variant	HERC1	GRCh38.p7	15:63666519	AATATCACTAGATAC[C/T]GTGAGTAAAAAGTGT	8925
rs143908646	snp	A/C/G	0.00716625	0.0594738	intron-variant	HERC1	GRCh38.p7	15:63816030	CCGGGTCCCTCCCCC[A/C/G]ACACGTAGGGATTAT	8925
rs143912369	snp	C/T	0.00835141	0.0640778	intron-variant	HERC1	GRCh38.p7	15:63776883	TAAATTTTGCCTCAA[C/T]AAATACTGAATAATG	8925
rs143944723	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63629487	GTAACAATAAATAAA[C/T]ATATACAAAAACATA	8925
rs143950608	snp	C/T	0.0119091	0.0762411	intron-variant	HERC1	GRCh38.p7	15:63783874	AGATCAAGACCATCC[C/T]GGCCAACATGGTGAA	8925
rs143960035	snp	C/G	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63620887	TGAGCCTATATGTGT[C/G]TCTGCATGTGAGATG	8925
rs143978354	snp	C/T	0.0182019	0.0936463	intron-variant	HERC1	GRCh38.p7	15:63796102	GTCTTTAAATAAATT[C/T]TGCTTCTAAGAGAAG	8925
rs143993221	snp	G/T	0.00119976	0.024463	intron-variant	HERC1	GRCh38.p7	15:63795536	GCTCTGATACAAAAG[G/T]TTCCTATTTTGAATT	8925
rs144000249	snp	C/T	0.0256215	0.110247	intron-variant	HERC1	GRCh38.p7	15:63645962	GACTCAAAAGGGATA[C/T]GTTATCTCTCATTAG	8925
rs144013506	snp	C/T	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63697746	AGGAGTGAGCCACCG[C/T]GCCCGGCCAATCTTA	8925
rs144013522	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	HERC1, FBXL22	GRCh38.p7	15:63608716	ATTCATGTAAAACTG[A/T]CCTTTCTAATGAACA	8925
rs144055754	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63760147	GGGACAACAGAAAGG[A/C]AAGATGGAAAGGAAA	8925
rs144063716	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63685823	CTGGCATGGGGGAAC[C/T]TGACTGGTAAACAGT	8925
rs144066815	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63805282	AAACAACACAATGGT[C/T]ATTCATTACAAGCAA	8925
rs144077302	snp	C/T	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63736677	ACAGTGGCACAATCT[C/T]GGCTCACGGCAACCT	8925
rs144094976	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63691952	GTAAGCAGACATTTT[A/C]GGGTAAGGACCAGGG	8925
rs144095244	snp	A/T	0.0501905	0.150254	intron-variant	HERC1	GRCh38.p7	15:63647677	TGCAGCCATAAAAAG[A/T]ATGAAATCAGGTATT	8925
rs144117980	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63797785	CAAAATGTTTACTGT[A/G]TACCTATGAGATTTC	8925
rs144119204	snp	A/T	0.0170251	0.090679	intron-variant	HERC1	GRCh38.p7	15:63755979	CCTACCTCATTACCT[A/T]ATACCACACCTGCCC	8925
rs144124865	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63762560	GAACTCCTGACCTCA[A/G]GTAATCCACCCACCT	8925
rs144127772	snp	A/G	0.00795532	0.062565	intron-variant	HERC1	GRCh38.p7	15:63688057	ATTTACAATTTTAAA[A/G]GATCATTCTGGATCC	8925
rs144129273	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63682513	CAGGGGCTCACACCT[A/G]TAATCTTAGCACTTT	8925
rs144158769	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63799019	AAGCGTCATCTCTGG[A/G]CTTACTTTTTAAGAT	8925
rs144162223	snp	A/G	0.0205511	0.0992634	intron-variant	HERC1	GRCh38.p7	15:63626348	TCTTTATCAGGGGGC[A/G]GAGAAAAAAATAAAA	8925
rs144166394	in-del	-/TTGTT	0.181058	0.240306	intron-variant	HERC1	GRCh38.p7	15:63681176	CTGAGACTAGGTGTA[-/TTGTT]TTGTTTTGTTTTGTT	8925
rs144198851	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63659637	TAATGTTGAACCATT[A/G]GTCTTATTTACTTTT	8925
rs144209038	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63822250	GGACTTTGCAGGTCA[C/T]GGCTAGGAATTTGGC	8925
rs144221369	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63727053	GAGGCTGAGGTGGGC[A/G]GATCACAAGGTCAGG	8925
rs144222228	snp	A/G	0.00755907	0.0610114	intron-variant	HERC1	GRCh38.p7	15:63612655	GATGCCTGCTCGTCC[A/G]CTCCCCAGACCCTCT	8925
rs144225154	snp	C/T	0.0119091	0.0762411	intron-variant	HERC1	GRCh38.p7	15:63653019	TATAGCTTTAAGGTA[C/T]TATGCACTAATGCAT	8925
rs144256848	snp	C/T	0.000149074	0.00863221	missense	HERC1	GRCh38.p7	15:63775097	ACAGGCATCATCCAA[C/T]TTTGTCTTAGAAGCG	8925
rs144294726	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63627882	ATTTCATAATAAATT[A/G]AAAATAAAACAAACA	8925
rs144325076	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63687221	GAGACTGACTAATCA[A/G]GATATCCCTGCAAGT	8925
rs144335858	snp	A/G	0.0547245	0.156101	intron-variant	HERC1	GRCh38.p7	15:63621620	ATTCTCCCACTTTCA[A/G]GTACACCAATCAGAT	8925
rs144359967	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63672830	AATTTCTATGAAAGA[C/T]TGACAGAAAAAAATA	8925
rs144361668	snp	A/C	0.00993419	0.0697739	intron-variant	HERC1	GRCh38.p7	15:63612893	CTAATCATATGTGCC[A/C]ATGTGCTGTCAAACT	8925
rs144453129	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63802491	CTTGCATTCTAGAAC[C/T]ACCAGTTCACAATCC	8925
rs144455613	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63820736	CTGCCTAGGCTAGTG[C/T]TGAACTCCTGTGCTC	8925
rs144463337	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63706352	AACTTTTTATTTCAA[C/T]GTGTGTGTACACGTG	8925
rs144465181	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63667032	GCTGTCTAGTGTTTC[C/T]AAGCACAAGGATGCT	8925
rs144520314	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63784859	CAGGTGATCAGCCCA[C/T]CTCGGCCTCCCAAAG	8925
rs144522472	snp	C/T	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63829051	CAGAGACAGAAGGAA[C/T]GGGAGAAGGTTAGAA	8925
rs144528859	snp	C/G	0.031825	0.122064	intron-variant	HERC1	GRCh38.p7	15:63762069	TTCCAATAAAAGAAA[C/G]CAGGACTTTTTTCAG	8925
rs144537688	snp	A/C	0.00275043	0.0369818	synonymous-codon	HERC1	GRCh38.p7	15:63658642	CACCACACGGTCATG[A/C]GGGTTTGCTAGGGCA	8925
rs144568031	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63773156	CGAAAAGACTAATCA[A/G]TGTAGGCCGGGTGTG	8925
rs144571029	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63702404	ATCAAAATATTTAAA[C/G]ATTAGGGGCGATAAT	8925
rs144593316	snp	A/G	0.0166325	0.0896639	intron-variant	HERC1	GRCh38.p7	15:63717749	TGGTGGTGCATGCCT[A/G]TAATCCCAGCTACTC	8925
rs144596922	in-del	-/G	0.0419251	0.138581	intron-variant	HERC1	GRCh38.p7	15:63809519	CACATCAGGAGCTGT[-/G]GATAACACTAAGATA	8925
rs144609799	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63715024	ATCAAAGCAATAAAC[A/C]CTCTCAGAGTCCAGA	8925
rs144619662	snp	A/G	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63644325	TCTGACTGGCCACTC[A/G]GTGTTTTAAACAATT	8925
rs144621797	snp	A/G	0.030665	0.119967	intron-variant	HERC1	GRCh38.p7	15:63825107	TGAGGCCGGGAGTTC[A/G]AGAGCAGTCTGGCCA	8925
rs144628956	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63712594	GAAGTCAGAACAAGA[G/T]ATTGAAACCATTAAC	8925
rs144629848	snp	C/G	0.0298908	0.118541	intron-variant	HERC1	GRCh38.p7	15:63759180	AGACAAGAATCCTAT[C/G]ATTCTTGAAACATAC	8925
rs144666966	snp	C/T	0.0150606	0.0854603	intron-variant	HERC1	GRCh38.p7	15:63822709	ACAGCCTATAAGAGG[C/T]CAAGTGAGAAAACAA	8925
rs144667147	snp	C/G	0.0341408	0.126114	intron-variant	HERC1	GRCh38.p7	15:63691232	GCACTTTGGGAGGCT[C/G]AGGCGGGCAGATCAC	8925
rs144669723	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63821383	CATAGCAAAACCCCA[C/T]CTCTACTAAAAACAC	8925
rs144672483	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63710846	TGTGTTGCAGATTCA[C/T]GCAACAGCTAAGAGT	8925
rs144682417	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63754206	TAGAGTAAAACATAT[A/G]TATGTCAAAACATAT	8925
rs144683590	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63640507	ATATTCTAAATTAAC[C/T]TACCGTAGTCTGAAA	8925
rs144732371	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63757102	ACATTATGGCAAGAA[C/T]CATATAAAATGTATT	8925
rs144739879	snp	C/T	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63752256	GTCATAAAACACTTT[C/T]ATACCACTGCCTGAC	8925
rs144810894	snp	C/T	0.00185722	0.0304165	intron-variant	HERC1	GRCh38.p7	15:63638794	GAAAAACAGGGGGTA[C/T]ATAATGATCAATTCT	8925
rs144821959	in-del	-/CA	0.0256215	0.110247	intron-variant	HERC1	GRCh38.p7	15:63734464	ATACTACAAATAAAC[-/CA]CAGAGTGTCTGGCTT	8925
rs144840751	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63751351	ATACCATATAGTCTA[A/G]GAGCGTAGTAGGCTA	8925
rs144848882	snp	C/T	0.0193772	0.0965046	intron-variant	HERC1	GRCh38.p7	15:63649213	CAAAAATTAGCTGGG[C/T]GTGGTGGCGAGTGCC	8925
rs144872006	snp	C/T	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63799100	CTTCAAATCAGTCAA[C/T]GACACGGAGTTGTTC	8925
rs144874174	snp	A/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63729735	TGATTTAAGCAGCAT[A/T]ATATGGGCTGGGTGC	8925
rs144886776	snp	A/G	0.0107246	0.0724382	intron-variant	HERC1	GRCh38.p7	15:63613404	CTCCTCCAATATTAT[A/G]CAGTAGTGCATACCC	8925
rs144899554	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63721742	GAGAATGACACAGAG[A/G]AAGAAAACTAGAGAT	8925
rs144959967	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63772254	GGTACCCTCTTCCCA[C/T]TAAGGAGCAATATTG	8925
rs144971124	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63701124	AATATAAAATGCGCA[A/G]GGAACTGATATTAGA	8925
rs144973995	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63831024	TGTTTTCAACATCAT[A/G]ATAATCTGCAATACA	8925
rs144996400	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63617634	CCACCAACAGTGTAA[A/C]AGTGTTCCTATTTCT	8925
rs145019690	snp	A/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63807584	AAACTCTACAACTAG[A/T]CCATTTATTTCCTGT	8925
rs145021293	snp	C/T	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63698410	GCAACGAGAGCGAAA[C/T]TCCGTCTCCAAAAAA	8925
rs145056564	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63805080	CTACTCCTTAGGTAT[C/T]TGCCCAGAAAAATGA	8925
rs145058589	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63736065	CCCCCCTCCCCAGAA[C/T]GGAAAGGAAAAAACA	8925
rs145073616	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63806188	TTTTTCTCTTTGAGA[C/T]AGGGTCTTGCTCTGT	8925
rs145077530	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63791552	ACATTTCCAATAAAA[C/T]TTTTAGTTACTGGAT	8925
rs145084621	snp	C/T	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63736936	TTACCCATGATTGGC[C/T]TCGAAGCCAAAGGTT	8925
rs145086846	snp	A/T	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63693784	GACTCTAAGCAGAGA[A/T]GTTTGGTCAGAAGCT	8925
rs145087801	snp	A/G	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63717689	CAGCCTGGTCAACAC[A/G]GTGAAACCCCATGTC	8925
rs145093863	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63688351	GGGAAGAAACAGAAC[A/G]TGATTAAGGGTGCCA	8925
rs145138918	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63824711	ACGTCTGTCAGTGGA[C/T]GGCTCTATAAAGAAA	8925
rs145139618	snp	A/C/T	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63660732	TTTGAAAAAAAAATA[A/C/T]ACCTAATAGAAATTA	8925
rs145139790	snp	A/G	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63803148	AGGCTGCAGTGAGCC[A/G]TAATTGTGCCCCTGG	8925
rs145148725	in-del	-/CGCGCG			intron-variant	HERC1	GRCh38.p7	15:63833744	CCGGCAAAGCACACA[-/CGCGCG]CGCGCACACACACAC	8925
rs145163667	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63665464	TTGAACCGGGGAGGC[A/G]GAGGTTGCTGCAGTG	8925
rs145172952	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63704222	AAAATCTCTTTGAAA[A/G]TATAATCTCCTAAAT	8925
rs145173323	snp	A/G	0.0287284	0.116357	intron-variant	HERC1	GRCh38.p7	15:63657288	TTTTTTTGAGACAGG[A/G]TCTCACTATGTTTCC	8925
rs145205291	snp	A/C	0.0119091	0.0762411	intron-variant	HERC1	GRCh38.p7	15:63782458	TAAATATTTTAAGCC[A/C]ACTGTTAAGACCTAC	8925
rs145211343	snp	A/C	0.0111196	0.0737302	intron-variant	HERC1	GRCh38.p7	15:63708176	CATCACTGTGTCAGG[A/C]AATAAAACATTTTCA	8925
rs145214136	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63753888	GATATAAAAAAGATA[C/G]TCATGCCGGGCACGG	8925
rs145225836	snp	C/G	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63681282	TCATGGCTCACTGAA[C/G]CGTCAAATTCCTGGG	8925
rs145237723	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63816850	TTCACAATTTTGCAA[C/T]CACTGATGAATTAAG	8925
rs145249014	snp	C/T	0.0107246	0.0724382	intron-variant	HERC1	GRCh38.p7	15:63720268	GCTACCACACTCGGC[C/T]TCTTCCCATTCTTTA	8925
rs145253016	snp	A/G	0.0345262	0.126772	intron-variant	HERC1	GRCh38.p7	15:63646933	GAAAAAATGCTCAAC[A/G]TCACTAATCATCAGA	8925
rs145264044	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63617614	GGTTGAACTAGTTTA[C/T]AGTCCCACCAACAGT	8925
rs145286513	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63793767	CAGTACAGAACCTCT[A/G]TGGGTTCAGCTATCT	8925
rs145286544	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63749303	CTGTTTTTATTAGTG[C/T]TTCTACTTTTTATTG	8925
rs145295831	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63622022	GTCCAGCTTTGTTCC[A/G]TTGCTGGTGAGGAGC	8925
rs145306352	snp	A/G	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63734151	CAGCGTGGATGACAG[A/G]GCAAGACTCTGTCTC	8925
rs145315975	in-del	-/CAACCA	0.0689305	0.172377	intron-variant	HERC1	GRCh38.p7	15:63629670	CTCTCAGTAAGAGTG[-/CAACCA]CAATGACGAGCAGCT	8925
rs145317697	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63660350	ATAAATAAATAAATA[A/C]ATACATACATACATA	8925
rs145348092	snp	A/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63678530	AAATGTCACAGACAC[A/T]CTGAAGTTAGTAGTG	8925
rs145348241	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63792092	TTTATATTCAATTGA[C/T]CAATATTCTCCAACC	8925
rs145364790	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63776573	TGGTTGCCTCTAGAG[A/G]GTGACAGCATGAACT	8925
rs145394094	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63793219	ATTCCCAGGAGGTTA[C/G]GCATTCTAAATCACA	8925
rs145406028	snp	C/T	0.0292243	0.117295	synonymous-codon	HERC1	GRCh38.p7	15:63674373	CCCAAACTGGTCTTC[C/T]AAAAGCCCATGAACC	8925
rs145440324	in-del	-/A	0.0640965	0.167152	intron-variant	HERC1	GRCh38.p7	15:63689197	TAAAGTAAGAAGTGG[-/A]AAAAAAAAGGATACA	8925
rs145444387	snp	C/T	0.0260105	0.111035	intron-variant	HERC1	GRCh38.p7	15:63693379	CTCCCAAGCAGCTGG[C/T]ACTACAGGCATGCGT	8925
rs145458067	snp	G/T	0.0205511	0.0992634	intron-variant	HERC1	GRCh38.p7	15:63791019	AAAAGTTTTTCAAAG[G/T]GTTGACTGTATCTAT	8925
rs145469037	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63715952	GCTCTCTTCCTCACC[A/G]CTCAGACGTCTTCGA	8925
rs145517328	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63645218	TTTAAACTTATTTGT[A/G]GTACATACAATCTTT	8925
rs145585192	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63641098	TTCAGTCTGATACCC[A/G]CATCCATCCCTATCC	8925
rs145585321	snp	A/G	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63684205	GTTAAGCTTTCTAGA[A/G]TAGTTGCAGTTTGCA	8925
rs145609815	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63820737	TGCCTAGGCTAGTGT[A/T]GAACTCCTGTGCTCA	8925
rs145611894	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63753239	AGGATGTTAACAAAC[A/G]AGCATTTTTATTACA	8925
rs145628440	snp	G/T	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63735344	TTAAGAATTACAGAA[G/T]TAGAACACATGGACA	8925
rs145629224	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63643659	ATAAAATTGGCAAGG[G/T]GGAGAGATAATTTCT	8925
rs145632130	snp	C/T	0.00953873	0.0683987	intron-variant	HERC1	GRCh38.p7	15:63650576	GCATATGTCACCACG[C/T]CTGGCTGTCTGTAAC	8925
rs145632417	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63662577	GCACTGGTTCCTAGA[A/G]TAAGGCATTACATTG	8925
rs145658811	snp	C/T	0.0162398	0.0886349	intron-variant	HERC1	GRCh38.p7	15:63622431	CTCCTGGGTTCAAAT[C/T]AAGTGATTCTCCTGC	8925
rs145661578	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63778116	AACTTGAAGATACAG[A/G]ATGCCAAAATTGCAA	8925
rs145661748	snp	C/T	0.00914312	0.0669923	intron-variant	HERC1	GRCh38.p7	15:63732085	CAGCTCACTTCAGCC[C/T]CTGCTCCCTGGTTCA	8925
rs145696170	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63639231	CATTTCAGTCAACAA[C/T]AAACTGCATGTGTGA	8925
rs145697123	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63772614	TTAAGAATCAGAAAA[C/G]AAAGTTAGAAAAACA	8925
rs145723838	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63741590	GGGATTACAGGCGTG[C/T]GCCTGGCCCTATGTT	8925
rs145731421	snp	C/T	0.0126979	0.078662	intron-variant	HERC1	GRCh38.p7	15:63644519	TTTTTTCTGTTTTTG[C/T]TTTTTACCCTCTCCA	8925
rs145732993	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63814581	CATACCTTAGCCACC[C/T]GAGTAGCTGGGATTA	8925
rs145755754	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63786977	TTGCCCAGTCGGTAG[C/T]GCAATGGCATGGTCT	8925
rs145764029	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63683333	AAAAACAAAACAAGT[A/G]TCTATAACTGGTGGG	8925
rs145774235	snp	C/T	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63622382	GCCCAGGCTGGAGTA[C/T]AGTGGCCTGATCTCG	8925
rs145801119	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63733810	TAAGCCATGATCGTG[C/T]CACTGCACTCCAGCC	8925
rs145826006	snp	C/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63806960	ACCATGTTGGCCAGA[C/G]TGGTCTTGAATTCCT	8925
rs145880094	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63628908	TGGTGGCAGACATAA[A/G]TAAGTTAATAACTGT	8925
rs145908223	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63665335	TCTGGAGTTCGAGAC[C/T]GTCCTGGCCAACATG	8925
rs145922289	snp	A/G	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63787193	ATGGAGTCTCACTCC[A/G]TCACCAAGGATGGAG	8925
rs145925300	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63711258	TGAGCTCAGGAGTTC[A/G]AGGCTGCACTGAGCA	8925
rs145926362	snp	A/G	0.00716266	0.059414	intron-variant	HERC1	GRCh38.p7	15:63665710	TATGAAATTTCTTCT[A/G]GCATGAAAACACCTA	8925
rs145955277	snp	G/T	0.00127461	0.0252127	intron-variant	HERC1	GRCh38.p7	15:63642910	CTATGATTTCTAAAG[G/T]TCCTTACAAGCTTAC	8925
rs145971585	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63709628	CTGAGTCAGATTTCA[C/T]AGCTGATTTCCCAAA	8925
rs145974555	snp	A/C	0.0366962	0.13039	intron-variant	HERC1	GRCh38.p7	15:63638400	TTTCTATTTTTTATC[A/C]TGTTAGTTACCTGTT	8925
rs145988571	snp	A/G	0.00636936	0.0560724	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835266	TACGGCACATATTAA[A/G]TACTCATTAAATGAT	8925
rs145989941	snp	C/G	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63725095	ATTTCTATTTCCTCT[C/G]GGGGCTCTTTTCACC	8925
rs145989988	snp	C/T	0.030278	0.119257	intron-variant	HERC1	GRCh38.p7	15:63769155	GGGCACAGTGGTTCA[C/T]GCCTGTAATCCCAGC	8925
rs146005427	snp	A/G	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63832578	CAACCACCACTAACA[A/G]AATTGTAAAAATATA	8925
rs146008811	snp	C/T	0.0252325	0.109451	intron-variant	HERC1	GRCh38.p7	15:63766735	CAGGCTGGAGTGCAA[C/T]GGCACGATCTCGGCT	8925
rs146027764	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63612070	GCACGCACCTGTAGT[C/T]CCAGCTACTGCGGAG	8925
rs146032767	snp	C/G	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63783116	TTAATTGATAATGCA[C/G]TAGCAGAGTTAGAGA	8925
rs146052857	snp	C/T	0.0260105	0.111035	intron-variant	HERC1	GRCh38.p7	15:63709146	TGCACACCACAACAC[C/T]CAGCTAATATATATA	8925
rs146075248	snp	C/T	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63696404	TGAAACTCTGTATGC[C/T]AAAAACAGTATTTTT	8925
rs146094675	snp	G/T	0.0260105	0.111035	intron-variant	HERC1	GRCh38.p7	15:63691392	GATCACTTGAGCCTG[G/T]AAGTGAGAGGTTGCA	8925
rs146109418	snp	C/G	0.00597247	0.0543191	intron-variant	HERC1	GRCh38.p7	15:63819045	CATCTTGGCCCATTC[C/G]TAATGCCAAGCACTT	8925
rs146113378	snp	C/G	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63750156	GTGTTTCTCACTATT[C/G]CGGTGAGATTTAAGA	8925
rs146113520	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63707011	ACATAGCTATAAGGA[A/G]GCTCAAGCACATATA	8925
rs146117218	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63616409	CAACACCAGTAGAAA[C/G]ATAGACTGGCCAGGA	8925
rs146129415	snp	A/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63815132	GGTCTTCATGCTTTC[A/T]ATCTTCACTAGGACG	8925
rs146133158	snp	C/G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63745086	GAGACTTGCGACTCT[C/G/T]ACTGGTCCCCTATCC	8925
rs146159060	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63613665	TACATAATAAAATTT[A/G]TTATATATATAAAAA	8925
rs146159842	snp	C/T	0.44638	0.154709	intron-variant	HERC1	GRCh38.p7	15:63618972	ttcctcttttcctaa[C/T]tgaatgccctttatt	8925
rs146169024	snp	A/G	0.00795532	0.062565	intron-variant	HERC1	GRCh38.p7	15:63817784	AATATAGATGAAACA[A/G]GACTGCCTATGAGTT	8925
rs146178551	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63638075	AAGGGGAGTGGTCGA[G/T]AAAATCTGGCTAAAG	8925
rs146188376	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63824293	AATCCCAGCACTTTG[A/G]GAGGCCGAGGTGGGC	8925
rs146197233	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63676313	GTCACTGGTTTCTTA[A/G]CTTGGTAGAATGGAG	8925
rs146213317	snp	C/T	0.040671	0.13668	intron-variant	HERC1	GRCh38.p7	15:63744043	GGTCTTGGACAAGAT[C/T]TGGGAGAATTCTCTG	8925
rs146216838	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63671472	GAAACTATTATTCCA[G/T]TAAGAGAGCTAACAT	8925
rs146233060	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63801368	CTGAGCCCTTAAACC[A/T]GTGTAGTCTGATGCT	8925
rs146235072	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63687306	GCAATTTGAGAGACC[A/G]AAGCGGGCGGATCAC	8925
rs146235462	snp	A/C	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63732653	CCCTTGCTCATTATT[A/C]TTCTCTCTAAAAATG	8925
rs146251714	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63798851	GTCAGTTTTTTATAC[A/G]CCCTAAGCATTTAGT	8925
rs146254132	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63728838	GAGGAAGAGGAGAGA[A/G]AAAAGGACTGTGACT	8925
rs146258344	snp	A/G	1.65726e-05	0.00287855	missense	HERC1	GRCh38.p7	15:63630578	CCAGCCAGGACAGGG[A/G]TTTGTTGCGGTCGAT	8925
rs146270564	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835646	GGTTTAAGCGATTCT[C/T]CTGCCTCAGCCTCCC	8925
rs146303170	snp	C/T	0.00795532	0.062565	intron-variant	HERC1	GRCh38.p7	15:63797840	AAATCCGTAAGATAG[C/T]TATTAATAACATAAA	8925
rs146317478	snp	A/C	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63657721	GACCAAGAAGCAATT[A/C]TTCTATGTTACCTTC	8925
rs146334190	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63727951	ACTCATTCAACAACT[C/T]TCTGTTGAACACCTA	8925
rs146351483	snp	A/G	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63788939	TAGGAGTTCATTCCA[A/G]GAATATAATGATGGC	8925
rs146373739	snp	C/T	0.0193772	0.0965046	intron-variant	HERC1	GRCh38.p7	15:63784252	TCAAATTGACTATTA[C/T]CTAACAAATAATTCA	8925
rs146375199	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63709825	ACATACTAATAATAC[A/G]TAAATAAGTCCAACA	8925
rs146379082	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63612829	CCTCTACCACAAAAT[C/T]TCAGCCCACTGGGGC	8925
rs146390156	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63819598	CTTCTAACATCTATT[C/T]CTCTCCTTGGCAAAA	8925
rs146393826	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63647279	AATTTACATTAAAAG[-/A]AAAAAAAAAACACAA	8925
rs146396801	snp	C/G	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63615557	AGAGGCTGCAGTGAG[C/G]TGAGACTGAACCACT	8925
rs146429961	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63796171	TGAAGAGGAACCTTT[A/G]TTTTTTACAAGTAGA	8925
rs146479868	snp	C/T	0.00163011	0.0285026	intron-variant	HERC1	GRCh38.p7	15:63649695	GGAAGTTGGAGACTC[C/T]GTCAGCTAGACGTAA	8925
rs146496018	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63721316	ATCACCTGAGGTCAC[A/G]AGTTCGAGACCAGCC	8925
rs146498400	snp	C/T	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63647793	TTTAAGTGGTTATTA[C/T]TAAAAAGACAAAAAA	8925
rs146515934	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63762739	AATCAAGCATTTATT[A/C]TGCTCTTCCCATATA	8925
rs146533626	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63807515	AATGGCTTCCCAATA[C/G]TGTTAGGCCTTGGGA	8925
rs146534491	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63738614	TGGTGGGAAAGCATA[C/G]AAGAAACAGCAGCAA	8925
rs146564750	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63628161	TTTGGGAGGCTGAGG[C/T]GGGCGGATCACTGGA	8925
rs146583633	snp	A/G	0.0150606	0.0854603	intron-variant	HERC1	GRCh38.p7	15:63631661	TCTCCCTGCCTCAGC[A/G]TCCCGAGTAGCTGGG	8925
rs146585741	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63708587	TAAACTTAGGGTTGG[C/T]ATTCTCTGTTTTAGC	8925
rs146616993	snp	A/G	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63703657	CTTTGGGAGGCCAAG[A/G]TGGGTGGACTGCTTG	8925
rs146634407	snp	C/T	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63700527	TCAAAATTCGTAACA[C/T]GGAGCTAATATTACA	8925
rs146651976	snp	C/G	0.0663309	0.169604	intron-variant	HERC1	GRCh38.p7	15:63833607	GGAGGCCTCTAGAGC[C/G]GGGGACCCGGGGGAT	8925
rs146652991	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63721882	TGCTTGTTTTTTGAG[A/G]CAGAGTCTCACTCTG	8925
rs146671124	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63830665	GGGGGAGCTTGGTGA[A/G]GAGTATGTAAGAACT	8925
rs146682137	snp	A/G	0.00636936	0.0560724	intron-variant	HERC1	GRCh38.p7	15:63610509	AGGGTTGTTTCCAGA[A/G]CTGAGTAGAAATGAG	8925
rs146687818	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63825120	TCGAGAGCAGTCTGG[C/T]CAACTTGGCAAAACC	8925
rs146700635	snp	A/T	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63613015	TTGAAAATAATTATA[A/T]CCTTTTTGTAAAAAT	8925
rs146713718	snp	C/T	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63767247	ACCTCAGGCAATCCA[C/T]CCGTCTCGGCCTCCC	8925
rs146736627	snp	C/G	0.0150606	0.0854603	intron-variant	HERC1	GRCh38.p7	15:63684060	TCTGAAAAACATCTT[C/G]GATGCTGGCTGGACT	8925
rs146738321	snp	C/G	0.0197687	0.0974348	intron-variant	HERC1	GRCh38.p7	15:63649107	CGCCTGTAATCCCAG[C/G]ACTTTGGGAGGCCAA	8925
rs146754363	snp	C/T	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63795956	AAGAGGAACAGGCTA[C/T]GACCTAATGCTTGCT	8925
rs146756256	snp	A/G	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63725601	CTACCGTACTGCAAT[A/G]AGATACTGATGCAAA	8925
rs146771747	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63816183	CAGAGATCAAATAAA[G/T]TTGGAAAATACTAAT	8925
rs146773108	snp	A/C	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63776940	GAAGTAAACAGACAT[A/C]TGTAGTTTATTTTGA	8925
rs146775525	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63704441	ATGAACTATTACTTA[C/T]AAACTTAACTAATAT	8925
rs146791752	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63779411	GCCAGGCATTATTTT[-/A]AAAACAAAATAGCAC	8925
rs146839378	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63666727	CCTCATCCAAGTTCC[A/G]TATTTGTAAATCTGT	8925
rs146843064	snp	A/G	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63609811	AAGGAAGGGGCAGTC[A/G]ATTAAACTCCAGTCC	8925
rs146856643	snp	A/T	0.031825	0.122064	intron-variant	HERC1	GRCh38.p7	15:63764773	ACAATAATTGACTGC[A/T]GCCAGCACCAGGGAA	8925
rs146858979	snp	C/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63664792	CCTGAGCAATAACTT[C/T]GTCTGATTTTGAATT	8925
rs146865746	snp	C/T	0.00716266	0.059414	intron-variant	HERC1	GRCh38.p7	15:63690271	ACATGTTTCTTCCTA[C/T]AGCGGTCCAAACCTA	8925
rs146876346	snp	G/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63781274	CACTTGACTTTACTG[G/T]GCTGTACAGATACTG	8925
rs146878597	snp	C/T	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63707588	CAGCAATTTCAATTG[C/T]ACTCTATCATACAAT	8925
rs146878704	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63660809	GACTTTTAAACCAGC[A/G]TTGTTGCTATTAAAT	8925
rs146904485	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63800514	ACAGTACAGTACCAG[A/C]GATATTAATTAGGTA	8925
rs146962649	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63689295	GGTTGAAGAGATAAT[C/G]AGAAGAAAGTGGCTG	8925
rs146978077	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63747429	CATGCCACTGCACTC[C/T]AGCCTGGGCGACAGA	8925
rs146978602	snp	C/T	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63704903	ACCACCACGCCCGGC[C/T]AATTTTTTGTATTTT	8925
rs146993500	snp	C/T	0.0138799	0.0821421	intron-variant	HERC1	GRCh38.p7	15:63813895	GAAACCCCGTCTCTA[C/T]AAAAAATGCAAAAAT	8925
rs146994508	snp	A/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63743127	TTTTCTTCATGAGAT[A/T]TTTCTTTAAGGCCAA	8925
rs147025302	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63832027	AGAATTACAAGAGGC[A/C]TTAATAGGCCATTTA	8925
rs147067861	snp	C/T	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63668407	CTGAGGTGGGAGAAC[C/T]GCTTGAGCCCAAGAG	8925
rs147080531	snp	C/T	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63800025	TGTAGTCCTAGCTAC[C/T]GGGGAGGCTGAGGCA	8925
rs147083603	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63685465	TGCACCTTATCATAA[C/T]ACCTCAGTCCTGGAC	8925
rs147083982	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63730771	AAATGATTTAGAGAG[A/G]GAGAACAAATTTGGC	8925
rs147096832	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63797378	TCCTCAATTACTCTT[A/G]TAGAGAAAATCATTA	8925
rs147100322	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63726564	GAATATTACAAATAA[A/C]TTTATGCCAATAAAT	8925
rs147113327	snp	A/G	0.00318978	0.0398085	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834912	TTCCAGAAGTTTGCA[A/G]TCCAATTGGAGGCGT	8925
rs147130639	snp	A/C	0.0182019	0.0936463	intron-variant	HERC1	GRCh38.p7	15:63773580	TGAGACAGATTCTCG[A/C]TCTGTTGCCCAGGAG	8925
rs147148078	snp	C/T	0.0170251	0.090679	intron-variant	HERC1	GRCh38.p7	15:63810367	AAATTTTGATATATA[C/T]TATGAGGAGATCTTT	8925
rs147164747	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63806302	CCACCTCACCTACAT[A/G]ATCTTTACCTGTCAA	8925
rs147176207	in-del	-/CTA	0.00874735	0.0655527	intron-variant	HERC1	GRCh38.p7	15:63814620	CACCATCACATCCAG[-/CTA]CTTTTTGTACTAGTT	8925
rs147205261	snp	C/T	0.00636936	0.0560724	intron-variant	HERC1	GRCh38.p7	15:63663657	AAAGACAGGGTCTTG[C/T]TATGTGGCCCAGGCT	8925
rs147221561	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63705555	TTCTGTTTTTTTTCT[A/G]TGGATGAGAAACCTA	8925
rs147221664	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63659204	AATAACAAGTTCTAT[A/G]AATCTTTTTATTGCT	8925
rs147237027	snp	C/T	0.0174175	0.0916809	intron-variant	HERC1	GRCh38.p7	15:63756252	GAATAATTATAAGAA[C/T]ATAAGAATTAAAATT	8925
rs147239190	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63683008	AGGCATGCTGATGCG[C/T]GCCTCCAGTCTCACC	8925
rs147246147	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63720098	AGTCAGGTGCTTTTT[C/T]TTCCCTTTTTTTTTT	8925
rs147252483	snp	C/T	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63794387	CTATGGAAGCTTCAT[C/T]ACTAGCTATTACTGG	8925
rs147270311	snp	A/G	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63793245	TCACAGGATGAGACA[A/G]GAGGTCGGCACAAGA	8925
rs147312545	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63646006	TAAGAGTTATCCTTA[C/T]TGACTAATAATCATT	8925
rs147327558	snp	A/C	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63760241	CACACAAAAAAAAAC[A/C]GAGGGAGGGAGTCTA	8925
rs147329416	snp	C/T	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63643826	AAAGTTCTAATTATC[C/T]CTCAGAGACAGGAAA	8925
rs147329532	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63685880	AACTGATACAGGCTG[A/G]CTTATTGTATCTAGA	8925
rs147344830	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63736752	GCTGGGATTACAGGC[A/G]TGCGCCACCATGCCC	8925
rs147346469	snp	A/G	0.0170251	0.090679	intron-variant	HERC1	GRCh38.p7	15:63664218	GTAGATTTTGAGAAA[A/G]TATATAAATGCTCTT	8925
rs147348338	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63621809	CTTGTGCATTCATCA[C/T]GTAGTTTTCGTGCCA	8925
rs147364859	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63625219	AATTTACTTTATTTC[C/T]CCGACCTCCCTTTCC	8925
rs147377413	snp	A/G	0.000332629	0.012892	synonymous-codon	HERC1	GRCh38.p7	15:63775324	TTTTCTAAGTGCCCC[A/G]GCAAATGGGGAATCT	8925
rs147432232	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63739849	TCAAACAAACAAATA[A/G]ATAAATAAATAAATG	8925
rs147449405	snp	C/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63719502	TACTCGGGGAAAAAT[C/G]AGAAGCAGCATTAGA	8925
rs147469276	snp	A/G	0.0236495	0.106139	intron-variant, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609286	GGAGAGAGACCCAGA[A/G]CCGTGACTGGGGACA	8925
rs147481039	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63822874	TAGACTGGTTAAAGG[A/G]TATAAAGAAAAAAGG	8925
rs147504046	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63711721	AACGCTAGCATTTCT[C/T]TATGAGCTGTCACAT	8925
rs147511471	in-del	-/T	0.0718919	0.175435	intron-variant	HERC1	GRCh38.p7	15:63824137	CAAAGAGACAAGAGA[-/T]TAAGTGTTGATGAGG	8925
rs147522411	snp	C/T	0.0138799	0.0821421	intron-variant	HERC1	GRCh38.p7	15:63682299	CTTGCTAGCTAAAGT[C/T]AGGAAAAAAGAGCAG	8925
rs147535606	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63794189	AGCAACCAGCAGCCC[C/T]TGGGGCTGTTCTGTC	8925
rs147538057	snp	C/T	0.00636936	0.0560724	intron-variant	HERC1	GRCh38.p7	15:63723626	CCTCTGAGCTATACC[C/T]TACAACTCTGGCGTT	8925
rs147572174	snp	A/C/G	0.000360221	0.0134162	intron-variant	HERC1	GRCh38.p7	15:63698709	GAGCTCTCATAAGGA[A/C/G]TAAATATCAAAGACT	8925
rs147572288	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63651517	AACCTTGGCTAGCAG[C/T]ATTTAACAGTTACAC	8925
rs147588494	snp	A/G	0.000581854	0.0170467	synonymous-codon	HERC1	GRCh38.p7	15:63694467	GTTTAGCAGACCAGT[A/G]GAAATTGCCAAAGAA	8925
rs147604605	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63752292	GTGGCCTCCTATACA[C/T]GACAGAATAAGTGGC	8925
rs147619698	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63817229	CAAATAAACTATAGA[C/T]CTATATCTATCTATA	8925
rs147621533	snp	C/T	0.00993419	0.0697739	intron-variant	HERC1	GRCh38.p7	15:63747438	GCACTCTAGCCTGGG[C/T]GACAGAGCAAGACAC	8925
rs147674868	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63751664	TTGATCATTATTTCA[C/T]GCTCAAGTTTAATGG	8925
rs147677350	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63678619	CAGAGATGTTAGGAA[A/T]ATTTGAAAGATGAAT	8925
rs147694097	snp	A/G	0.000879267	0.020949	synonymous-codon	HERC1	GRCh38.p7	15:63674385	TTCCAAAAGCCCATG[A/G]ACCACTAATTTATAG	8925
rs147706742	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63803247	AAAAAGTACTTGTAT[C/T]ATCCCCATTTTCCAG	8925
rs147723012	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63800195	TCTCCACTAATGCAT[A/T]TGTTAATATTTTTCT	8925
rs147735150	snp	A/G	0.00597247	0.0543191	intron-variant	HERC1	GRCh38.p7	15:63634577	AAATATGAATTTCAC[A/G]TTGGGAAACAGTTAA	8925
rs147780378	snp	C/T	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63733671	CCAGCCTGGGCAACA[C/T]AGCAAAACCCCCTCT	8925
rs147782358	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63660225	CTCAGGAGGCTGAGA[C/T]CGGAGAATTGCTTGA	8925
rs147811925	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63791308	ATGTTCCAATGAGCA[C/T]CTCCTTGGTATATTA	8925
rs147815112	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63824294	ATCCCAGCACTTTGG[A/G]AGGCCGAGGTGGGCA	8925
rs147829701	in-del	-/C	0.0659589	0.169201	intron-variant	HERC1	GRCh38.p7	15:63820924	ATCATTAGGGGACAA[-/C]CAAATAGCTTAAACA	8925
rs147829785	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63787527	AACTGAGGGTATGTT[A/G]CTGAAAGAAGAGAGA	8925
rs147839298	snp	A/G	0.0182019	0.0936463	intron-variant	HERC1	GRCh38.p7	15:63614363	GAAAAATGGCACCCA[A/G]GAGTGCCTGGCACCA	8925
rs147856000	snp	C/G	0.00914312	0.0669923	intron-variant	HERC1	GRCh38.p7	15:63617440	TGGTTCCAAGTCTTT[C/G]CTATTATGAATAGTG	8925
rs147857286	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63618528	AAGTAGTTTTTTCCA[-/A]TTCTGTGAAGAAAGT	8925
rs147886362	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63715089	CATTGGTGTTTGGGG[A/C]AGACCTGCTTCTAAT	8925
rs147905057	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63640897	TCACTTTCCTCCTTT[A/G]TAAGAGAATCCTGGT	8925
rs147932476	snp	A/G	0.00398564	0.0444627	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834490	CAATCACATAAAAGC[A/G]TTTCACTTGACCTAC	8925
rs147951638	in-del	-/AT	0.0138799	0.0821421	intron-variant	HERC1	GRCh38.p7	15:63701905	TGAAAAGGGCATTAA[-/AT]AAGCTTCTACATAAC	8925
rs147983531	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63821016	CGATGAACAATTATA[C/T]GCTCTTGATAATGTT	8925
rs147992883	in-del	-/A	0.0681886	0.171594	intron-variant	HERC1	GRCh38.p7	15:63810424	CATTTGTGTAAAAAT[-/A]AAAAAAAAGAGGGGC	8925
rs148026313	in-del	-/GC	0.0711525	0.174681	intron-variant	HERC1	GRCh38.p7	15:63785687	GTGGGATGATCCCTT[-/GC]GCGCTCAGGAGGTCA	8925
rs148054016	snp	C/T	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63773336	GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	8925
rs148058998	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HERC1	GRCh38.p7	15:63669348	ACAGCACATTATTTC[A/T]CTCCGAAATGGCCAT	8925
rs148073051	snp	C/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63787939	GTACTCCAGTCTTGG[C/T]GACAGGGTGAGACCC	8925
rs148090474	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63765757	ATATATTATGTCGCC[C/G]TAAAATGTATAAAAG	8925
rs148095131	snp	C/T	0.000513283	0.0160118	synonymous-codon	HERC1	GRCh38.p7	15:63663071	AAACATAGCTTCCAT[C/T]GCCTCATCATCAAGA	8925
rs148108223	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63801129	ATGCCCCTACCCCCT[C/G]TATCTTGCCCTATGC	8925
rs148110100	snp	G/T	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63779121	AAATAATTAGAAAAA[G/T]ATAAGAAAAAAGAAT	8925
rs148111551	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63704628	AAAATTTAATTCCTA[A/G]GTCAAAATGAACTAC	8925
rs148121104	snp	C/G	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63615323	AATATAAATACAAAG[C/G]AATCACCAAGTGCGG	8925
rs148128516	snp	A/C	0.00216386	0.0328215	synonymous-codon	HERC1	GRCh38.p7	15:63718682	TTCTGATAAGTGTTT[A/C]CCAGGTTGATATCTA	8925
rs148130477	snp	A/G	0.000827872	0.0203286	intron-variant	HERC1	GRCh38.p7	15:63645702	AAATGGAAGGAAGAG[A/G]AAAAAAATCAGAGTA	8925
rs148143152	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63826629	CAGAACTAATGGACT[C/T]TACCTGCACATAATA	8925
rs148144973	snp	C/G	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63760146	AGGGACAACAGAAAG[C/G]AAAGATGGAAAGGAA	8925
rs148149215	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63656570	AAGTATTGGCATATA[C/T]TTGAAGTACAATTGA	8925
rs148175383	in-del	-/ATAT			intron-variant	HERC1	GRCh38.p7	15:63826833	ATATATATATATATA[-/ATAT]TATATATATAAAGTA	8925
rs148179105	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63808137	ACAAAAAAAAAAAAA[-/A]TACATCACTACAATG	8925
rs148219329	snp	C/T	0.00504465	0.0499687	intron-variant	HERC1	GRCh38.p7	15:63643084	ATATATTTACCAATA[C/T]ACACCATTGAACTGT	8925
rs148255834	in-del	-/AC	0.00256476	0.0357183	intron-variant	HERC1	GRCh38.p7	15:63747887	TAAGAAAATAATAAA[-/AC]AGTCTTAAAATGAAA	8925
rs148265171	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63805326	CATTATTATTCATTA[C/T]TTGGAGATTCAACAT	8925
rs148270894	snp	A/G	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63709246	AACTCCTGGGCTCAA[A/G]CAATCCTCCCACCTC	8925
rs148272811	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63637447	GGCAAAGGTTTGTAC[A/G]ACCAAACCTACATTA	8925
rs148285303	snp	A/G	0.00239473	0.03452	intron-variant	HERC1	GRCh38.p7	15:63818142	TTTATAGCTCTCTGT[A/G]AAAAAAAGTGTTTAA	8925
rs148300727	snp	A/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63797852	TAGTTATTAATAACA[A/T]AAAACAATTTTCAAA	8925
rs148303476	snp	A/G	0.0271762	0.113356	intron-variant	HERC1	GRCh38.p7	15:63727201	GAATCACTTGAACCC[A/G]GGAGGCAGAGGTTGC	8925
rs148315043	snp	A/G	0.0150606	0.0854603	intron-variant	HERC1	GRCh38.p7	15:63618293	GTTTCTGTCAGGTTT[A/G]TCAAAGATCAGATAG	8925
rs148317251	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835146	TGTGACCTTGGGCAA[A/G]TTGCTTGACCTCTCT	8925
rs148338552	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63754849	TCATAGAGTCACTTC[A/G]GTGAACCATTAGAAT	8925
rs148340070	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63682196	GAAGGTGGACTGCTA[C/T]CTGTTGTGAGGGGCA	8925
rs148354835	snp	A/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63794068	GCCATGACAGTTTAC[A/T]AATCCCATGGCACTG	8925
rs148358840	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63694996	TATGCTAGAGCCTTA[C/T]GATGGTTTTTAATTA	8925
rs148367628	snp	C/T	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63623025	CAACCAACAATTTCA[C/T]ACTTTATTTTTGTGG	8925
rs148404160	snp	G/T	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63766882	AGGTTTCTCCATGTT[G/T]GTTCAGGCTGGTCTG	8925
rs148408533	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63664298	ATGAATGTATGCTAC[A/G]ATTTAAATAAAATTA	8925
rs148410422	in-del	-/TG	0.0554779	0.157039	intron-variant	HERC1	GRCh38.p7	15:63740694	TTGAACATTTTTTCA[-/TG]TGTTTACTGGCTATT	8925
rs148423349	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63780435	ATTAAAAAGGTAAAA[C/G]AGAAGGCCGGGCGCG	8925
rs148424795	snp	A/T	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63706460	AATAACCCCTTTCCA[A/T]CATAATGGAATGTAC	8925
rs148434448	in-del	-/A	0.0599851	0.162463	intron-variant	HERC1	GRCh38.p7	15:63684709	ACCTTCTAGCGGGGG[-/A]AAAAAAATCTATGTT	8925
rs148440053	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63814915	TGCAATGTACTAATG[A/T]GAGCTATGATTATTA	8925
rs148454377	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63829124	CCATGGTTTTAAATA[C/T]ATATAGAATACAGGC	8925
rs148459081	snp	C/G	0.0205511	0.0992634	intron-variant	HERC1	GRCh38.p7	15:63732808	ATGTTTTTCCCCTTG[C/G]GGGAGAGGGGTCTAG	8925
rs148543977	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63757424	CGCGCCATCATGCCC[A/G]GCTAATTTTTGTAAA	8925
rs148547017	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63683627	ACTTAAAACACTATT[A/G]TCAGGTCCTACACCA	8925
rs148580730	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63710003	AACTTTTAAGGCAAA[C/T]AGTGCTTTAGCAAAG	8925
rs148583089	snp	C/T	0.0287284	0.116357	intron-variant	HERC1	GRCh38.p7	15:63639017	GTGATTCAAAGCTAG[C/T]CATGTGTTTTCTGAA	8925
rs148594083	snp	A/G	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63819748	TGGATGGGGTTTTCT[A/G]TCAGCCAAAACTATG	8925
rs148596597	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63751352	TACCATATAGTCTAG[A/G]AGCGTAGTAGGCTAC	8925
rs148610951	snp	A/G	0.0659589	0.169201	intron-variant	HERC1	GRCh38.p7	15:63799389	CTTGTAGTCCCAGCT[A/G]CTCAGGAGGCTAAGG	8925
rs148613637	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63729830	GAGGTTGAGACCAGC[C/T]TGGCCAACATGGTGA	8925
rs148634728	snp	A/T	0.0115144	0.0749975	intron-variant	HERC1	GRCh38.p7	15:63666659	CATCCATTTATGTTA[A/T]ACTTTGTAAAGATTT	8925
rs148649234	snp	A/G	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63784008	GAGGCAGAGGTTACA[A/G]TGAGCCAAGATTATG	8925
rs148665947	snp	A/G	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63795686	TTTATACTTTCTGCA[A/G]AAAGGGTATACTCGC	8925
rs148683878	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63626571	ATGGAAATGGGAAAC[C/T]TAGCAGAGCCAACTC	8925
rs148707616	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63744162	TGTGTGTGTGTGTGT[C/G]TGTCTCTCTCTCTCT	8925
rs148718351	snp	C/T	0.0138799	0.0821421	intron-variant	HERC1	GRCh38.p7	15:63822580	AACAGAGCAAGACTC[C/T]GTCTCAAAAAAAAAA	8925
rs148737911	in-del	-/AAC	0.306679	0.24349	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835425	TGAAGCATACTCAAA[-/AAC]CAACAAGCAAAAGCT	8925
rs148738870	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63678750	ACATTTTACATTGTT[C/G]AAGGGGTGCAAAAGT	8925
rs148756062	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63720363	GGGTGGGAGAGTTAT[A/T]GTCCACCCTGCTCCC	8925
rs148793071	snp	A/G	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63672861	TTCTTACTTATATAC[A/G]TCTTTGTATTCACTA	8925
rs148806789	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63612695	TCAGACCGCCAGGCA[C/T]GAGAGTCAGTCAAAA	8925
rs148807778	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63790509	CATGAACCAGGGAGG[C/T]GGAGCTTGCAGTGAG	8925
rs148810841	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63651034	AAAAAATTTAAGTTT[A/G]TAACTACTAGGTTAG	8925
rs148858182	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63759981	GGAGGATAGTGGGGC[C/T]AAGGGAGTCAGAATT	8925
rs148862688	snp	A/C	0.0252325	0.109451	intron-variant	HERC1	GRCh38.p7	15:63655335	CTCCAGTTTGGGTGA[A/C]AGAGTGAGACTCTGT	8925
rs148895440	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63711439	ACTATAAGACTGGGA[A/G]TATGAAGTGGAAGCA	8925
rs148906157	in-del	-/AGAG	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63704397	TTCCATATGCATGAT[-/AGAG]ATTTGAGAGAAAACA	8925
rs148911174	snp	A/T	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63753740	TTTAGTCATTCATTG[A/T]GTTGTTAATACTGAA	8925
rs148914239	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63725894	ATCCATTAAAATGAC[A/G]TTCAAGATTGTTTAA	8925
rs148930928	snp	C/T	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63704625	CCAAAAATTTAATTC[C/T]TAAGTCAAAATGAAC	8925
rs148943963	snp	A/C	0.00914312	0.0669923	intron-variant	HERC1	GRCh38.p7	15:63813049	CATCAACTTACAATC[A/C]ACGATATTGAGATAC	8925
rs148947660	snp	C/T	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63741629	TGAGTTTTACAGTTA[C/T]AGCTCTTATATTTAG	8925
rs148951519	snp	C/T	0.0256215	0.110247	intron-variant	HERC1	GRCh38.p7	15:63644556	CTAACCCTAGCTTCA[C/T]GAATTTATGTTACTC	8925
rs148978446	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63796997	CCATCATGGCCGGAA[C/G]TAGTTTATCAGGTTA	8925
rs148981615	snp	C/T	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63771493	TGGAGTGCAATGGTG[C/T]GATCTCAGCTCACTG	8925
rs148983737	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63699243	AGTGTCTCTGTAAGC[A/G]CTTTAGCAACACGCT	8925
rs148998587	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63807041	ATGAGCCACCACACC[C/T]GGCCTGAGTGATTTT	8925
rs149003032	snp	C/G	0.0225045	0.103662	intron-variant	HERC1	GRCh38.p7	15:63629077	GCCTCAGCCTCCCAA[C/G]TGGCTGAGATTACAG	8925
rs149021186	in-del	-/CA	0.261332	0.249743	intron-variant	HERC1	GRCh38.p7	15:63802157	TGGTCCAGGTCTCCC[-/CA]ACTCCTGCCACATGT	8925
rs149066495	snp	G/T	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63793836	CTCCACCTTGAGTAG[G/T]AGCTGGGTAAAATGA	8925
rs149069045	snp	A/G	0.02016	0.0983543	intron-variant	HERC1	GRCh38.p7	15:63722462	TCTCCCTTATCCATG[A/G]TCTTGCTTTTCATGG	8925
rs149103648	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63748110	ATATGCCTGTAGTCC[C/T]AGTTACCCAGGAGGC	8925
rs149105560	snp	A/C	1.75847e-05	0.00296514	intron-variant	HERC1	GRCh38.p7	15:63675126	TGGGAAGCTTTAATA[A/C]AGATCAGAATGACAC	8925
rs149115234	in-del	-/G	0.207253	0.246318	intron-variant	HERC1	GRCh38.p7	15:63639985	TCACTATGGAGGCCT[-/G]TGCCATCAGATTGAA	8925
rs149119833	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63791723	TAAGCTGTAAGCCCA[G/T]TCACACCAACTATAA	8925
rs149123900	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63613635	CCTATATTATCGTGT[G/T]GTACACCTTAAATAT	8925
rs149124309	snp	A/G	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63688597	TCTTTGAGAAGGAAT[A/G]GGGATTAATCCAACA	8925
rs149133583	snp	A/G	0.00358779	0.0422022	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835037	TAGATACATGTTTGT[A/G]TGTCACATGAGGCAG	8925
rs149141397	snp	C/T	0.0154538	0.0865337	intron-variant	HERC1	GRCh38.p7	15:63665486	GCTGCAGTGAGCCGA[C/T]ATCGCGCCACTGCAC	8925
rs149158124	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63708480	TCTGTTTTCATATGC[G/T]AAATCAAATCCTGCC	8925
rs149189404	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63831089	CCAAAGTTGTGTAGA[C/T]CTTTGTTGTTGTTTG	8925
rs149195507	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63660508	ATAAGTTGACAGCAA[C/T]AGCAAATGCTACAGC	8925
rs149209181	snp	A/G	0.0193772	0.0965046	intron-variant	HERC1	GRCh38.p7	15:63776760	TGCTTGAGCTCAGGA[A/G]TTTGAGACCCGCCTG	8925
rs149244618	snp	A/G	0.0295035	0.117819	intron-variant	HERC1	GRCh38.p7	15:63705931	GCTACTTGGGAGGCT[A/G]GAGTAGGAGGATCCC	8925
rs149258971	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63740604	TAGCCAGCCTTTTTG[A/G]TTACTGTCACTTAGT	8925
rs149259307	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63814845	TGAAACCTACCTGTC[C/T]ACGTCTCAAAATTGT	8925
rs149261140	snp	A/C	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63743974	CTTGGGTATTATGAT[A/C]TAAACTGTATCTACG	8925
rs149265192	snp	C/T	0.000510943	0.0159753	intron-variant	HERC1	GRCh38.p7	15:63645457	ATATAAAAACTAAGA[C/T]GTATAGATGCAAATT	8925
rs149281975	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63685336	CAGGTCACATTGGTA[C/T]CATGTTAACCTGTGC	8925
rs149295956	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63772896	TTACCTATGATAAAA[C/T]TGTAAAACATGACCC	8925
rs149298022	snp	A/G	0.00795532	0.062565	intron-variant	HERC1	GRCh38.p7	15:63702213	AATACACTACCACAC[A/G]AGAATCAGAAAACAA	8925
rs149311133	snp	A/C	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63809586	TCCTGGGCCACTGCA[A/C]AAGTTGAGTTGAGAA	8925
rs149322499	snp	A/C/T	0.000224472	0.010592	intron-variant	HERC1	GRCh38.p7	15:63630417	CCAACTGAGGAACAC[A/C/T]GTGAGATTTCTAGAA	8925
rs149325973	in-del	-/AAGA	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63809010	CTAAAATAAAAAATG[-/AAGA]AATAGCAAAAATATC	8925
rs149338563	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63615471	AAAGATTAGCTAGGC[A/G]TGGTGACACATGCCT	8925
rs149348648	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63800945	ACCTCAAGGGAGAGG[A/G]AAAGGGGTGGAGATA	8925
rs149349707	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63731915	AAAAACAACAGGAAA[C/T]ACGTGTACAATGTAC	8925
rs149419636	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63750615	AAGACTGCTGCTGAG[A/G]GATTAAACCACTTCA	8925
rs149436663	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63793057	ACCAGATGAAGAGGA[C/T]AGGGCAGGATATGGG	8925
rs149440780	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63691012	GTTATGTAACTTGAC[C/T]AAAGCCACACAAGCT	8925
rs149457868	snp	C/T	0.00268061	0.0365119	missense	HERC1	GRCh38.p7	15:63666030	CCTAGAACGGCTGCT[C/T]CAGGCCTAGAGTCTG	8925
rs149476899	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63681679	TGCTGAATACCTGCT[C/G]TCCTTCTGGGAGTAT	8925
rs149508555	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63736429	TTCTAGCAGTAGCTT[A/C]GAAGAGCCTTCCTTT	8925
rs149513509	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63636860	AGAGCCAAGGACCAG[C/T]AGAACCCATAGGAAC	8925
rs149515322	snp	C/T	0.00795532	0.062565	utr-variant-3-prime	HERC1, FBXL22	GRCh38.p7	15:63608648	TGCTTTATTTCTCTG[C/T]ATAAGGAACCCTGAA	8925
rs149525266	snp	A/C/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63779494	AGAAACACTAATAAC[A/C/G]TGAGACATGAATATA	8925
rs149561732	snp	A/G	0.0314385	0.121371	intron-variant	HERC1	GRCh38.p7	15:63767773	TTTGGAGAGTTCTCC[A/G]AAGAGCTGAGTATTA	8925
rs149568447	snp	C/T	3.31417e-05	0.00407059	synonymous-codon	HERC1	GRCh38.p7	15:63612512	GAGGAGGGACAGCAG[C/T]GGCACAGGAACAATC	8925
rs149598534	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63658154	TCATCCCCTTTTTAC[A/G]TTACACTCCACAGTA	8925
rs149627794	snp	A/G	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63789667	GCTAGGCGTTGTGGC[A/G]GGCACCTGTAATCCC	8925
rs149630766	snp	A/G	0.0726307	0.176182	intron-variant	HERC1	GRCh38.p7	15:63714619	CAGTGGCACGATCTC[A/G]GCTCACTGCAACCTC	8925
rs149645302	snp	A/G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63822048	CTCTACAGGGGTGAA[A/G/T]TCTGAGGCACTCTCT	8925
rs149649237	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63726975	TAGCAAGTTCTGAGA[C/T]GCTTTAGAAAAGAAT	8925
rs149651001	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63652921	TCTCAAAATTCTGGG[A/C]TTACAGGCATAAGCC	8925
rs149660606	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63802296	AGAAAAAACTTTTTC[A/G]TTGTTATTATTGCTA	8925
rs149698595	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63699073	TAGATAAGGCTGAGT[A/G]CTGCTACCATAACCA	8925
rs149716514	in-del	-/AAAAAAGAAA			intron-variant	HERC1	GRCh38.p7	15:63652036	GCGAGACTCAGTCTC[-/AAAAAAGAAA]AAAACAAAACAAAAC	8925
rs149727749	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63682845	GATTAAAAAAAAAAA[-/A]GATGCAAAGGCTGGG	8925
rs149747079	snp	A/G	0.0652144	0.168387	intron-variant	HERC1	GRCh38.p7	15:63793691	CTGTGGACTCGCCCT[A/G]AATTCTTTCTTGCGC	8925
rs149749785	snp	C/G/T	0.0376037	0.131863	intron-variant	HERC1	GRCh38.p7	15:63766741	GGAGTGCAATGGCAC[C/G/T]ATCTCGGCTCACTAT	8925
rs149752142	snp	C/G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63692103	CAAGAAGCAAGGTCG[C/G/T]AATCTGTGCTAAAAT	8925
rs149767093	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63741371	TTCTTGTCTCCCAGG[C/T]TGGAGTGCAATGGTG	8925
rs149769838	snp	C/T	0.0197687	0.0974348	intron-variant	HERC1	GRCh38.p7	15:63667580	TAATTTATTATGGAG[C/T]TTATGTGTAAAAGTG	8925
rs149788276	snp	A/G	0.00716266	0.059414	intron-variant	HERC1	GRCh38.p7	15:63683091	CAGGGAGCCGAGCTT[A/G]TGCCACTGCACTCCA	8925
rs149801962	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63795024	TTAGCCAAGATTGTG[C/T]CACTGCATTCCAGCC	8925
rs149804637	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63725067	AATATGACAGAGTAG[A/G]ACCAGACCTACAATT	8925
rs149807676	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63825766	AAAAAGAAAAATAAT[-/A]AATTTTTTTTTTTTT	8925
rs149817817	snp	A/G	0.00398564	0.0444627	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834485	AAGTTCAATCACATA[A/G]AAGCGTTTCACTTGA	8925
rs149819842	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63806466	CACATGTACATTTAT[A/C]ATACTCTGCCTGGTT	8925
rs149825836	snp	G/T	0.00719997	0.0595663	intron-variant	HERC1	GRCh38.p7	15:63638703	CAGTTATCTTCATCT[G/T]TACTGACCTCAGGTC	8925
rs149832660	snp	C/T	0.0150606	0.0854603	intron-variant	HERC1	GRCh38.p7	15:63609806	CACATAAGGAAGGGG[C/T]AGTCAATTAAACTCC	8925
rs149842268	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63677838	AGTGTAACTCAACAG[A/G]TCATACCTGATAGTA	8925
rs149868040	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63626244	GCATACAGAGAAGTT[A/G]AGATAATTACACAAT	8925
rs149886825	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63613177	GCCAATTATTAACTC[C/T]CTTAATTTTTCCGTC	8925
rs149912176	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63660339	AAATAAAAACAATAA[A/G]TAAATAAATAAATAC	8925
rs149913864	in-del	-/C			intron-variant	HERC1	GRCh38.p7	15:63705667	CAGGCTTTTAGAAAA[-/C]CTGCCACTAGTGGCA	8925
rs149914693	in-del	-/TTCT	0.0142736	0.0832652	intron-variant	HERC1	GRCh38.p7	15:63746015	TCAATTGTTTTTCTG[-/TTCT]TTATTTTTTTAATTT	8925
rs149942173	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63791489	TCTTTTTCAAAACAA[A/G]ATCAGCAGAGGGAAG	8925
rs149958011	snp	A/T	0.0260105	0.111035	intron-variant	HERC1	GRCh38.p7	15:63824499	AGATCATGCCACTGT[A/T]CTCCAGCCTGGGCAA	8925
rs149963604	snp	A/C	0.00597247	0.0543191	intron-variant	HERC1	GRCh38.p7	15:63729097	ACTACCCCCAAACCA[A/C]GACTAAAGGAATCTT	8925
rs149965482	snp	A/G	0.000115953	0.00761333	missense	HERC1	GRCh38.p7	15:63654150	TCCAATTTGATAAAG[A/G]AGCATTTTCTAAGAT	8925
rs149979885	snp	C/G	0.0252325	0.109451	intron-variant	HERC1	GRCh38.p7	15:63707826	CCCAGCTACTTGGGA[C/G]GCTAAGGCAGGAGAA	8925
rs149998268	snp	A/G	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63720122	TTTTTTTTTTTTAAG[A/G]GACAGGGTCTCACTC	8925
rs150014831	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63761860	GGAAGAAGATATAAA[G/T]GTAAAGGTTAAGTAA	8925
rs150032998	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63703493	TTCCTCTCATCAGGC[G/T]TTTAGTAATTCAAGA	8925
rs150035605	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63672411	AACACCAAGATTCAG[C/T]TGGGCATACTATTCA	8925
rs150054418	in-del	-/GT			intron-variant	HERC1	GRCh38.p7	15:63832271	ATAGGTGCAGAATAC[-/GT]GTGTGTGTGTGTGTG	8925
rs150072390	in-del	-/CGCG			intron-variant	HERC1	GRCh38.p7	15:63833744	CCGGCAAAGCACACA[-/CGCG]CGCGCGCACACACAC	8925
rs150097513	snp	A/C	0.0825414	0.185628	intron-variant	HERC1	GRCh38.p7	15:63788759	CCGTCTCTACTAAAA[A/C]TACAAAAATTAGCTG	8925
rs150116696	snp	G/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63796494	ATCGATCATTCCGGG[G/T]TGTAGACTGTAAACC	8925
rs150117727	snp	C/T	0.00636936	0.0560724	intron-variant	HERC1	GRCh38.p7	15:63725964	AGATCCAGACCCATG[C/T]TTTCTTTTTTTCTGG	8925
rs150131204	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63808370	ACAGCTCACTGGAGC[C/T]TTGAACTCCTGGGTC	8925
rs150134694	snp	C/G	0.0150606	0.0854603	intron-variant	HERC1	GRCh38.p7	15:63739333	CTCCCAAGCGGCTAG[C/G]ACTACAAGCACACGC	8925
rs150138601	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63640968	TTTAGGATCACTGTC[C/T]GGACAAGTTCAAACG	8925
rs150152353	snp	C/T	9.84165e-05	0.00701417	intron-variant	HERC1	GRCh38.p7	15:63753101	CTATAAAAACAAACA[C/T]ATTAAACAATTTACT	8925
rs150155057	snp	C/T	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63680000	AGAAGAAATAGCTTA[C/T]TATATTTATAAACTC	8925
rs150185598	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63628581	TTGATGGTTTCACAA[C/T]GATGCTGGATACAGT	8925
rs150203913	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63615458	TACCAAAAAATAAAA[A/G]GATTAGCTAGGCGTG	8925
rs150223831	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63663358	TTATACCTATCACGT[A/G]TGTTTCCTCTCTTGC	8925
rs150270591	snp	A/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63827547	TATAGTATACTCTCC[A/T]CATAAAAAAGAAGGG	8925
rs150273788	snp	C/T	0.00914312	0.0669923	intron-variant	HERC1	GRCh38.p7	15:63731650	TAGTGATCAGCCTTT[C/T]AATGTGGGCGGGATA	8925
rs150288191	snp	C/T	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63783754	ATAAAAGCAGTAGAC[C/T]GTGACTCCCCAAAGA	8925
rs150310250	snp	G/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63722180	CTATAAAATTAATTT[G/T]CTCAAATAATATTAG	8925
rs150324932	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63830911	AGTAAACAACTACTT[C/T]ATGCTCTTTTTCACT	8925
rs150326607	snp	C/G	0.00189815	0.0307486	intron-variant	HERC1	GRCh38.p7	15:63764092	AGCCACGATTATTAC[C/G]TACCTCTTCAAAGAG	8925
rs150346795	snp	A/C	1.66463e-05	0.00288494	missense	HERC1	GRCh38.p7	15:63674731	TGTTCATGATTTTTT[A/C]TTTTCCCTTCTGTTA	8925
rs150363835	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63716984	TGCTAAGGACAATGT[C/T]AACTTGATTTCCCAC	8925
rs150377972	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	HERC1, FBXL22	GRCh38.p7	15:63608118	GCTAGCAGTTGCTGG[C/T]CTTTCTGTAACACCT	8925
rs150432716	snp	C/T	0.0182019	0.0936463	intron-variant	HERC1	GRCh38.p7	15:63701923	GCTTCTACATAACAA[C/T]TGAGACTAAGCCCAA	8925
rs150484048	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63633710	GTGGGCATTCAAGAA[C/T]GCACAACAGAAGCTT	8925
rs150502906	snp	C/T	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63743542	TGCTGGGATTACAGG[C/T]GTGAGCCACCATGCC	8925
rs150504709	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63670806	ACACCTGTAATACCA[C/G]CATACTTTGGGAGGC	8925
rs150532313	in-del	-/AA	0.0704125	0.17392	intron-variant	HERC1	GRCh38.p7	15:63817141	AGATGAAGAGAGTCT[-/AA]AGATTTAAAATGATG	8925
rs150535457	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63737083	TAAGACAGAACGGGA[A/G]GCTACTAAAAAAGGA	8925
rs150573235	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63691953	TAAGCAGACATTTTA[C/G]GGTAAGGACCAGGGA	8925
rs150589145	snp	A/T	0.000149428	0.00864245	synonymous-codon	HERC1	GRCh38.p7	15:63732969	CTTCATCAAAATTTC[A/T]GCCAGGTGGGTATCT	8925
rs150621547	snp	C/T	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63819947	ATAAGTTTAAACGTG[C/T]GTTAAATAATACATG	8925
rs150625374	snp	A/C	0.02016	0.0983543	intron-variant	HERC1	GRCh38.p7	15:63724526	TTTTCTTTTCTTTTC[A/C]GCTCTCCTTCTTTCC	8925
rs150627357	snp	A/G	0.00636936	0.0560724	intron-variant	HERC1	GRCh38.p7	15:63649451	TAACTTTCAAAGGAG[A/G]CTTGGAATCTGCTAT	8925
rs150637962	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63832304	CTCTATACATATATA[C/T]GTACATTTATGCATA	8925
rs150641424	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63766573	GACAGAATGAGACTC[C/T]GTCTCAAAATAAAAA	8925
rs150656711	snp	C/G	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63780751	AAAACAGAGACTAAA[C/G]GTTAGCTGTAAGACC	8925
rs150675624	snp	A/C	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63792555	TACTTTAAACTCCTA[A/C]AATTTTGGCATTTTT	8925
rs150678107	snp	A/C	0.0322114	0.122752	intron-variant	HERC1	GRCh38.p7	15:63719054	ACTTACTGTTCCAAG[A/C]GCTGTGGATATAGCA	8925
rs150696805	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63609669	CCCCCACAGAGCAGG[C/T]AGAATGGAAAGAACG	8925
rs150707627	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63805983	AACCCAATTACTTGC[A/G]GGCCCTGCCTCTTGT	8925
rs150712946	snp	G/T	0.0158469	0.0875917	intron-variant	HERC1	GRCh38.p7	15:63709437	CTCCATTGATCTGTT[G/T]TCCCCATTTATAATT	8925
rs150783298	snp	A/T	0.0287284	0.116357	intron-variant	HERC1	GRCh38.p7	15:63653445	GTTAAAAAAAAACTG[A/T]TTAAGTAATACAATT	8925
rs150797724	snp	A/G	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63769489	TATAGCCCATTAAAT[A/G]TATAACTTCATTTGT	8925
rs150800103	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63697987	ACTTTAAGGCTATGC[A/C]AACATCTTATGTCTC	8925
rs150819294	snp	C/T	0.00795532	0.062565	intron-variant	HERC1	GRCh38.p7	15:63646281	TCTTCATGAACGGAA[C/T]TTCTGACATTACTGG	8925
rs150833060	snp	A/G	0.0298908	0.118541	intron-variant	HERC1	GRCh38.p7	15:63761433	TAAAAATAAAAATAA[A/G]AAAATTAGCCAGGTG	8925
rs150836233	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63686902	GAGAAGGCAGTAAGC[A/G]GCTGGTCAAATGAGA	8925
rs150851093	snp	A/C	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63798376	TACAATCAGGAATTA[A/C]AGTGTTTTCCAGGTA	8925
rs150867346	snp	C/G/T	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63810876	CCTCCTGAGGTGATT[C/G/T]AAGGAGTACATAACA	8925
rs150869193	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63740388	TAATGCTGTTATTAA[C/T]ATTCATGTACAAGTT	8925
rs150871017	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63714345	TAAAGGTCTTTGCTG[A/G]AACAGAATTTAGTTT	8925
rs150872039	snp	A/G	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63624423	TTATTTTGGCTGGGC[A/G]CAGTGGCTCATGCCT	8925
rs150884843	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63821766	TCAGATAATCTAATT[C/T]AGAGACAGTTTTACT	8925
rs150887620	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63755161	GTAAATCTGCTCTCA[C/T]GGCTTCTCAGTAACT	8925
rs150939207	snp	G/T	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63725903	AATGACATTCAAGAT[G/T]GTTTAATGCTTTTTA	8925
rs150944919	snp	A/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63616925	ACAGCACATGGACTA[A/T]ATTCTGAACTATTTT	8925
rs150953452	snp	C/T	0.00279162	0.0372561	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834359	CCAGGCGAAGGGACA[C/T]GTGTTACGGCCGGCG	8925
rs150959717	snp	C/T	2.05691e-05	0.00320689	intron-variant	HERC1	GRCh38.p7	15:63664629	AGCAACACAAAGTTT[C/T]TGAAACCATTATGGA	8925
rs150975911	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63679449	AAACCTGAAAGCTTC[C/T]ACTACATAATGGCTA	8925
rs150990163	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63793492	AAAAGGGGGAGGAAC[A/C]CTCAGTTTCGGGAAT	8925
rs150998047	snp	A/G	0.0154538	0.0865337	intron-variant	HERC1	GRCh38.p7	15:63622043	GGTGAGGAGCTGCGT[A/G]ATCATTCTGTTTTTA	8925
rs151005555	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63829379	AGTAAGCTATGATCA[C/T]GCCACGGCACTGCAG	8925
rs151016679	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63611876	CATAGTTTGTTTTCC[C/T]CAACATAAAAGCAAC	8925
rs151025071	snp	G/T	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63785297	GGCATGGTGGTACAC[G/T]ACTGTGGTCCCAGCA	8925
rs151028198	snp	A/G	0.00755907	0.0610114	intron-variant	HERC1	GRCh38.p7	15:63710138	GAATCTTTGATTTCC[A/G]AGTAGGCAGTGCAGT	8925
rs151039144	in-del	-/A	0.0655868	0.168795	intron-variant	HERC1	GRCh38.p7	15:63783526	ATACACTGAGAAACC[-/A]AAAAAAACTGTGTGA	8925
rs151135181	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63648298	AATGATAATGCAACC[A/C]TTGCAAGTAAATTTC	8925
rs151149290	snp	C/G/T	0.0233268	0.105743	intron-variant	HERC1	GRCh38.p7	15:63763347	TAATGGAAGAATACA[C/G/T]GTATACAGACATAAC	8925
rs151151600	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63688826	ATTCCCAGGAATTTG[C/T]GTTTGGGAAACTAGG	8925
rs151165121	snp	C/T	0.0667028	0.170006	intron-variant	HERC1	GRCh38.p7	15:63799423	GAGGATCACTTGAGC[C/T]CAGGAGGTCAAGGCT	8925
rs151170432	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63703307	TTCAACAGCGTGAAT[C/G]TTAGTATCCCCACTG	8925
rs151185904	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63716711	TTGATTAAAATATCA[C/T]GCTGTAAATTTATTC	8925
rs151192416	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63626936	AGTAGGTGCTATTAT[C/T]ATCCTCATTTTACAG	8925
rs151199681	snp	A/G	0.113685	0.209567	intron-variant	HERC1	GRCh38.p7	15:63824316	AGGTGGGCAGATCAC[A/G]AGGTCAGGAGATGGA	8925
rs151202543	snp	A/G	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63757835	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	8925
rs151238719	snp	G/T	0.0193772	0.0965046	intron-variant	HERC1	GRCh38.p7	15:63746333	CTGTACTTTCTATTA[G/T]TACCTACCAAAAGAG	8925
rs151240521	snp	C/T	0.00953873	0.0683987	intron-variant	HERC1	GRCh38.p7	15:63673810	GCTCACTGTAACCTC[C/T]GCCTCCCAGGTTCAA	8925
rs151245685	snp	G/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63633512	CAGCTGCATGCAGAG[G/T]GTTACAAAGGATTAC	8925
rs151255311	snp	C/T	0.0205511	0.0992634	intron-variant	HERC1	GRCh38.p7	15:63791012	ATCCTAAAAAAGTTT[C/T]TCAAAGGGTTGACTG	8925
rs151322641	snp	C/T	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63803635	AAGGTTTTAATGAAC[C/T]AATTGCCAATTCAGT	8925
rs151323780	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63735110	CCTGGTAAGGCTCTG[C/T]GCAAAGTGATTTGGG	8925
rs180672540	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63714836	ACAGCCGTGAGCCAC[C/T]GCACCTGGCCCAAAG	8925
rs180678282	snp	G/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63746706	GAAAAACCAAATCTG[G/T]TGGGAGAGCAGGAAT	8925
rs180679938	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63737891	GCAATGACTTCACAA[C/G]TCTTACTGAAAAATG	8925
rs180686628	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63787077	GAAGTCCTGACCTCA[A/C]GTGATCTGCCTGCCT	8925
rs180691518	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63768071	TCCCTCACTTCTCAG[A/G]TAGCTTTCAATAACT	8925
rs180693070	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63704989	GTGATCCGCCCACCT[C/G]AGCCTCCCAAAGTGC	8925
rs180701297	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63729151	TTCCTATTCCAGAGG[C/T]TTCTGGCTCTCTTAA	8925
rs180714793	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63684995	GCCTGGGTGACAGAG[C/G]AAGACTCCGTCTCAA	8925
rs180737389	snp	A/T	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63817153	TCTAAAGATTTAAAA[A/T]GATGTAATAAACATG	8925
rs180752092	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63807801	ACCTTTGTGCCCCCA[C/T]TCATGCTGTTGTCCT	8925
rs180758778	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63760319	GGAAAACTAATCCTA[C/T]GTAGAAATAAGCAAC	8925
rs180770156	snp	C/T	0.00795532	0.062565	intron-variant	HERC1	GRCh38.p7	15:63827034	GATACCAAAATACTA[C/T]GCGCAAGGCTATTTA	8925
rs180771950	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63779049	GAAGAATGAATTATA[A/G]AAGTGTTCAAGGAAG	8925
rs180777219	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63798240	TTCTCCCCAGTTCTA[C/G]TGTATCCTCCATCTT	8925
rs180822944	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63663582	TGTCTCAGCCTCTGA[A/G]TAGCTAGGACTACAG	8925
rs180834092	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63617850	CGCCCACTTTTTGAT[A/G]GGGTTGTTTTTTTCT	8925
rs180862267	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63641927	TTTCTTCAGAACCTG[A/C]AGAATAAGGCATCTA	8925
rs180908875	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63804009	AACTGATGCTTATCT[A/G]AAGTGTCAAGGCAGT	8925
rs180916460	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63823628	TCTCAATTCTCACAA[A/G]GATGGTACATAACTA	8925
rs180959993	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63647426	TTAGTACAAACTCTA[C/T]AGAAAACAGTATGGG	8925
rs180972038	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63625179	TTGTTACTGGACTAG[C/T]CCATAAAGATAGACA	8925
rs180976351	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63709163	AGCTAATATATATAT[A/T]TATTTTTTATTTTTT	8925
rs180984838	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63669951	TGGGGGAATACAGCC[A/G]TTAGCAAAATAGATG	8925
rs180987499	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63637953	AGCAGAAACTCGTAC[A/G]TAAGAATGAGTCATG	8925
rs180998588	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63657736	CTTCTATGTTACCTT[C/T]AATAAACTTTATTGA	8925
rs181007420	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63764559	ATACTCCCCATGGGT[A/G]TATTGCCCACCTGCC	8925
rs181016987	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63742548	CTTTATTTTATTCCT[C/G]ATCTTAGGGGGAAGG	8925
rs181018117	snp	G/T	0.00200274	0.031581	missense	HERC1	GRCh38.p7	15:63689606	GTAGTTTTATTTCTT[G/T]TTCTTTTTCCTTTAT	8925
rs181033389	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63791511	AGAGGGAAGTTCAAA[G/T]AACAAAATAGAACAT	8925
rs181047196	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63782148	ACCTAAGGTAACTGA[C/T]GAAAGTAGTTATATT	8925
rs181049979	snp	A/C	0.0154538	0.0865337	intron-variant	HERC1	GRCh38.p7	15:63833545	GTCTCTCGGCCCTCT[A/C]CGCGGGCGCCTCGGC	8925
rs181060838	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63722228	CAAACTTGCATAGTA[C/T]TTTACCATGGTACTT	8925
rs181061204	snp	C/T	0.00597247	0.0543191	intron-variant	HERC1	GRCh38.p7	15:63811645	AAACCCCGTCTCTCC[C/T]AAAATTATACAAAAT	8925
rs181073920	snp	A/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63681200	TTTGTTTTGTTTTGT[A/T]TTGTTTTTAATTTTC	8925
rs181076096	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63700922	TGTAAAAAATATATA[C/T]ATTCTTTTTTCATTT	8925
rs181080396	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63732289	TACAGGCATAAGACA[A/C]CGCGCCTGGCCTGAA	8925
rs181081154	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63773934	AAATTGATTATACTA[C/T]GCTATTTTATTATTT	8925
rs181082646	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63752703	AAGGGAAGCTAAATG[C/T]TAAAACATTTTAGAA	8925
rs181103738	snp	A/G	0.000399281	0.0141238	missense	HERC1	GRCh38.p7	15:63774746	CAGTCAAAGCTGATC[A/G]TTCCTTCCTGGCTTG	8925
rs181117978	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63813692	CCCAGGACATTACCA[C/T]TGTATGCCTGTGTTT	8925
rs181123426	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63793844	TGAGTAGGAGCTGGG[C/T]AAAATGAGGCTGAGA	8925
rs181129135	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63617156	CTAATGCTATCCCTC[C/T]CCGCTCCCCTCACCC	8925
rs181188852	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835877	AGGACTGCTTACTTT[A/G]AAGACCAATCAAGAG	8925
rs181193834	snp	C/T	0.0138799	0.0821421	intron-variant	HERC1	GRCh38.p7	15:63822894	AAGAAAAAAGGAGAA[C/T]CATAGATCACTTAGG	8925
rs181214508	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63763361	ATGTATACAGACATA[A/C]CACCTGAGACTGATC	8925
rs181225906	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63803863	TATCTGACTTTTAAG[C/T]TTATTATTAATATAA	8925
rs181244935	snp	C/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63781639	CAATATTGAAATTAG[C/G]CCAACTAATAACCCT	8925
rs181280581	snp	A/C	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63613680	ATTATATATATAAAA[A/C]AAAACTGGGCCAAGT	8925
rs181285874	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63647125	CCAGTTTGGTGGTGG[A/G]TGCCTGTAATCCCAG	8925
rs181324745	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63720546	AGATAAAAATGTTAT[A/G]TGCTGGTTTTCATTT	8925
rs181330669	snp	C/T	0.00597247	0.0543191	intron-variant	HERC1	GRCh38.p7	15:63700240	TATTGCTAATATTCA[C/T]CCACATTACTAAGTG	8925
rs181341411	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63656947	TCCCTACAGATGACA[A/G]TCAGGCGGTTTCCAA	8925
rs181343009	snp	G/T	0.00755907	0.0610114	intron-variant	HERC1	GRCh38.p7	15:63680931	ATAACACGAAAATAA[G/T]CGCATCAATTTAGAA	8925
rs181356382	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63636913	CTGCTGTGCTCTTCA[C/G]ACTCAGATCACAATG	8925
rs181364209	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63781114	TGGTAATGATGAACA[A/G]TATAATCACTAATAA	8925
rs181372005	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63763121	CCCCTGGTGTCCCAC[A/C]TTTCTCTCTCAAACT	8925
rs181375039	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63710140	ATCTTTGATTTCCGA[C/G]TAGGCAGTGCAGTCA	8925
rs181379582	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63753741	TTAGTCATTCATTGT[A/G]TTGTTAATACTGAAA	8925
rs181379844	snp	C/T	0.00015338	0.00875594	intron-variant	HERC1	GRCh38.p7	15:63732878	CTTGACTAAAGAGAT[C/T]CCTACCCCTTTATTC	8925
rs181383179	snp	C/G	0.000556216	0.0166673	synonymous-codon	HERC1	GRCh38.p7	15:63689673	CCACATACAATCAGA[C/G]AGAAGGGAAAATAAG	8925
rs181391581	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63624635	AAGGAGGTTGAGGCT[G/T]CAGTGAGCTGAGATA	8925
rs181404086	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63670529	GTTCGCCCAGTAAGA[A/G]CCAAGTGCAACTCTA	8925
rs181448099	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63741921	AGTTGGAAAGTGTGA[G/T]CCTTCTAACTTTCCT	8925
rs181496036	snp	A/G	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63741068	GACTCTTGCCCTGTC[A/G]CCCAGGCTGGAGTGC	8925
rs181503156	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63699674	TTTACTGTAAAATGA[C/T]ACCTATATAAAATTA	8925
rs181503927	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63647762	ACAGAAAGGCAAATA[C/T]TACATTTTTTTCACT	8925
rs181507070	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63625807	GTCCAGCAGCATCAT[A/G]TCCAACCTCTAGACT	8925
rs181565103	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63774257	TGTTAGCTCCATGGG[G/T]GTGGAAACTGTATCC	8925
rs181567479	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63812620	TGAAAATAAATCCAT[A/C]CCTGTGGAACTCATG	8925
rs181573300	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63816882	AGTCTAAGCAATTAT[C/T]ATCAACAGCTGCTAA	8925
rs181641279	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63719757	AGATCAGATCTGTGA[C/T]GTGAGAATATGAGAG	8925
rs181647203	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834740	CCAAGTGGACATTAA[A/G]TTGTTGAGTGAATAC	8925
rs181665127	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63778298	GATTTGGAGTGACTC[C/G]CAGAAAGATTAAATC	8925
rs181673625	snp	C/T	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63759922	AGTATCTGAGGACAG[C/T]TGCCAGTCCCTAATA	8925
rs181674162	snp	A/G	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63793481	CTATATGGTCTAAAA[A/G]GGGGAGGAACCCTCA	8925
rs181684665	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63796961	AGGAGGGTATTATGA[A/G]GCATATCTGGCTCCC	8925
rs181695266	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63704061	AGGTTCAACTGCCCA[A/T]CTGAAGATTTTATGG	8925
rs181700029	snp	A/C	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63661407	AAAGTCTGTTTTTTT[A/C]ATCAGGAAAAAGATC	8925
rs181702043	snp	C/T	5.54165e-05	0.00526357	intron-variant	HERC1	GRCh38.p7	15:63656053	TCAGTCAGAAATAAT[C/T]AATGTAACGGGGAAA	8925
rs181704742	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63684504	CTCTTGCATCCAACC[A/C]TTCTGGACAAAAAGG	8925
rs181709165	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63640799	ATCTAAGCTATCACA[C/T]TGCATATAGTACATT	8925
rs181713153	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63613252	CTGTATATGAGTAAC[C/T]ACATGAAATTCTGTG	8925
rs181727951	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63828326	GAGAGAGTGACACTT[C/T]TCAGTACAACTTTTT	8925
rs181783996	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63680365	AAAAATCTTATTGGG[A/G]TTTTACTATCTTCCT	8925
rs181815436	snp	A/C/T	0.000466378	0.0152638	intron-variant	HERC1	GRCh38.p7	15:63636154	AAGCCTGGAACAGAA[A/C/T]AGAAACCCAACAGGA	8925
rs181825858	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63676028	CCTGCCTTAGCTCCC[C/T]GAGTAGCTGGGATTA	8925
rs181827714	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63777852	TTTTTTAAAAACCTG[A/G]GTCTTTAGTCCATCT	8925
rs181844021	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63808308	TTCTTTCCTCAAAGA[A/C]ACAGGGTCTTGCTCT	8925
rs181854192	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63630720	GATCAGTCATTTAGC[G/T]TATTATGGTGGAATG	8925
rs181859827	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63827440	AAAAAAAAAAAGACC[A/G]AAGAAAATGAAAGGA	8925
rs181922428	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63713141	TATATATACGAAAAA[C/T]TGTGCCTCCTCATTT	8925
rs181923471	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63758788	CATAAAAGTGACAAA[A/C]TGCACAAAAGAGTCA	8925
rs181942168	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63737080	GTGTAAGACAGAACG[C/G]GAGGCTACTAAAAAA	8925
rs181949481	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63694603	TAAACAAAGCATTTA[C/T]TAAAATGAATAATTT	8925
rs181950698	snp	C/T	3.58333e-05	0.00423265	synonymous-codon	HERC1	GRCh38.p7	15:63643002	AACTTCTGGAATCCA[C/T]ACTGTGGTCTGAATA	8925
rs181952425	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63618808	CTCTGTCTGTTATTG[C/G]TGTATAAGAATGTTT	8925
rs181954878	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63651862	CCAACATAGTGAAAC[C/T]CTGTCTCTACTAATA	8925
rs181956438	snp	G/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63675317	GTGATACTAAATGCA[G/T]AAGCAATGAGATGCT	8925
rs182037773	snp	C/T	1.76521e-05	0.00297081	intron-variant	HERC1	GRCh38.p7	15:63729389	AAGAAAAAAAGTTCC[C/T]AAATTACTACTTTGA	8925
rs182039619	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63769849	CATCAGAGCAAGACT[C/G]TCTGTCTTAAAAAAT	8925
rs182043846	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63796473	ATTTCGCTTCTAACC[G/T]CCATCATCGATCATT	8925
rs182086261	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63695440	GCCCAGGCTGGAGTG[C/T]AGTGGGGTGATCTTC	8925
rs182087895	snp	A/G	0.0197687	0.0974348	intron-variant	HERC1	GRCh38.p7	15:63771534	CTCCCAGGTTCAAGC[A/G]ATTCTCCCTGCCTCA	8925
rs182095388	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63809634	AAGAGGAACAATATA[C/T]TGAACTTGTACGGAG	8925
rs182101951	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63789993	AGGAAAACCCCAAAA[A/C]GTCTGTCAGAACAGC	8925
rs182102635	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63695979	CTACTGCATTATTTA[A/G]GAAATGGAACCAAGG	8925
rs182113114	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63747687	ACACGCGCGCGCACA[C/T]ACACACACAAAGATA	8925
rs182115986	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	HERC1, FBXL22	GRCh38.p7	15:63608196	TCTTTAATTCCATCA[C/T]GTGCTCATTTTGTCT	8925
rs182117598	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63730728	GCTTAAATACTTAGC[A/G]GCAGCCAGCCATCTG	8925
rs182120501	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63677477	ACAAAATGCAATGAA[C/G]AGATTAGCTGGCTGG	8925
rs182130706	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63653054	ATTATCTGAGACCTA[C/T]TATAATCTTTACTAA	8925
rs182130764	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63631253	CTAGAGGGTGCCAGC[C/T]AGCCCCTGATGCGCA	8925
rs182168760	snp	C/T	0.00755907	0.0610114	intron-variant	HERC1	GRCh38.p7	15:63737626	CTCAGGTGGTCCGCC[C/T]GCCTCGGCCTCCAAA	8925
rs182190188	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63685837	CTTGACTGGTAAACA[A/G]TCCCCTATACTGATA	8925
rs182205322	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63785100	GACTCAAATAAATAT[A/G]TAAAGACTCAAATGC	8925
rs182213160	snp	C/G	0.00795532	0.062565	intron-variant	HERC1	GRCh38.p7	15:63766722	CACTCTTGTTGCCCA[C/G]GCTGGAGTGCAATGG	8925
rs182214818	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63806361	CTCAAAGGTGACTTC[C/T]TCCATGAAGCTTTTC	8925
rs182238064	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63744727	GTGAATACTGCCTGG[C/T]CTAGGTCTCACCCTT	8925
rs182252541	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime	HERC1, FBXL22	GRCh38.p7	15:63608758	TGTACAATTTCATGT[C/T]CACTGGGTGGATTTA	8925
rs182270041	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63825476	TATGTATATCAAAAC[A/G]TCATGTGTACACATT	8925
rs182297620	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63788025	GCCAGTTTCATCAAA[C/T]TGAACTCAAAGGAAA	8925
rs182309859	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63747135	TAAAAGTGCCTGTGC[C/T]ATCCAGTTTGGGTAA	8925
rs182325388	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63816557	ACATCAGTGACCAGC[C/T]CCATACTCTAAGTCA	8925
rs182368415	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63665598	ATTAAAATGAATACT[C/T]GATTTTATATCACTT	8925
rs182383885	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63621818	TCATCACGTAGTTTT[C/T]GTGCCACGGTTTTCA	8925
rs182407063	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63629241	AGGTGTGAGCCACCA[C/T]GCCCAGCCCCCAATA	8925
rs182442842	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63706089	GAAAAATGCTTAAGA[A/G]AGTTTTTAGTTATCA	8925
rs182452902	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63664805	TTTGTCTGATTTTGA[A/G]TTCTTCCAACAACAA	8925
rs182456322	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63724233	TCTCAGGAGGTCCTT[C/T]AGGACTGTCACAAGG	8925
rs182458238	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63707042	ACTCTGAAACACTAA[C/G]TAAAAAACTCACATT	8925
rs182466681	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63672468	CACAGGCATCAGTAT[A/G]GCAGACATTAAAGGT	8925
rs182470065	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63702611	GTTTTATCAAAGTAC[A/C]AAATTACTAACATAT	8925
rs182477523	snp	C/T	0.00676609	0.0577691	intron-variant	HERC1	GRCh38.p7	15:63754424	TGAGTCATTCTACAC[C/T]AGGCATATATAACTG	8925
rs182477745	snp	C/T	0.00636936	0.0560724	intron-variant	HERC1	GRCh38.p7	15:63659459	GGTCTCACCATGTTG[C/T]CCAGCCTGGTCTTGA	8925
rs182479476	snp	C/T	0.00993419	0.0697739	intron-variant	HERC1	GRCh38.p7	15:63649165	CGAGACCATCCTGGC[C/T]AACATGGTGAAACCC	8925
rs182480543	snp	A/C	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63682388	GGGCCCAAATATTCC[A/C]ACAAGTGGGCTTTAG	8925
rs182489962	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63627231	TCTAAGAAACAAAAT[C/T]CCTATGGGGAATCTT	8925
rs182571768	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63639641	GAGGTTGTTAGATCA[C/T]GTGCTGTCCTGTAGT	8925
rs182587471	snp	A/G	0.000387102	0.0139069	intron-variant	HERC1	GRCh38.p7	15:63615937	TAGGAACAGAAGAAA[A/G]CAGAATTTTTATTAC	8925
rs182609220	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63755652	AGGCATGGTGGCGCA[C/T]GTCTATAGTCCCAGC	8925
rs182613789	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63793915	CCACAGGATGAGATA[A/G]GAGGTCAGCACAAAA	8925
rs182614197	snp	C/T	0.00169067	0.0290255	synonymous-codon	HERC1	GRCh38.p7	15:63686389	CCCAGAAGTTACTCC[C/T]GTAGATGCCAATCCA	8925
rs182628640	snp	C/T	0.000399281	0.0141238	missense	HERC1	GRCh38.p7	15:63645054	TGGTCTGTGTAGTAT[C/T]TTGAGGAATGCGCCA	8925
rs182651932	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63828841	AGAAAATAACTAACC[C/T]AAGTAACTTTGGAAA	8925
rs182741386	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63711475	ATATTAATGCAGATG[A/G]AGGAGAAAAGGAGGA	8925
rs182750585	snp	G/T	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63615255	AATTCAGAACCGATT[G/T]AAGGCACTGGGTATG	8925
rs182858808	snp	C/G	0.000100183	0.00707682	intron-variant	HERC1	GRCh38.p7	15:63649676	AAAAAGCTAAGTCTA[C/G]AAAGGAAGTTGGAGA	8925
rs182861181	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63673970	CCTCAAGTGATCTGC[C/T]CACCTCGGCCTCCCA	8925
rs182861457	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63813836	ACTTTGGGAGGCCGA[A/G]GCAGGTGGATCACCT	8925
rs182879560	snp	C/T	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63775816	GCCAAAGTGGGCAGA[C/T]CACTTGAGGCCAGGA	8925
rs182899640	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63765933	TTTCTAAACTGATAG[A/T]GAAAGATCAATTTCT	8925
rs182901100	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63804458	GGGCATGGTGGCGGG[C/T]GCCTGTCATTCCAGC	8925
rs182903367	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63756340	CCAAAGGGTTGAAGG[A/G]GCAACTGCAGAAAGA	8925
rs182916591	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63794619	CCAAAGATTTTAGGA[A/G]TTATATTCCAGGAGA	8925
rs182920162	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63776289	CATATCCAAAACTGA[A/G]CTCCTATTCTACCAG	8925
rs182925340	snp	C/G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63711938	GCTACCAATTAACTC[C/G/T]AAGTCCAAAGTTCCT	8925
rs182935581	snp	G/T	0	0	synonymous-codon	HERC1	GRCh38.p7	15:63734829	CATGGTTGCTCCCAC[G/T]GATAAAGTTTCAATT	8925
rs182938556	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63691325	ACAAAAATTAGCTGG[C/G]AGTGGTGGTGCACGC	8925
rs182970616	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63614824	GGATAACTCAAATGA[A/T]ATAGAAAATGCATTC	8925
rs182973347	snp	A/C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63643837	TATCCCTCAGAGACA[A/C/G]GAAAATACTGACTAC	8925
rs182978313	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63620798	TAAAGTTGTTTTATC[A/G]GAGACTAGGATTGCA	8925
rs182992874	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63805419	GGTTCTAGCTGCATG[A/T]AATTCTAGAGTAAAA	8925
rs183015026	snp	A/T	3.33261e-05	0.0040819	synonymous-codon	HERC1	GRCh38.p7	15:63690640	TAAGTTACCAACCAG[A/T]GGGATACCTGGAGGG	8925
rs183035079	snp	C/T	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63729963	CCCAGGAGGCAGAGG[C/T]TGCAGTGAGCCAAGA	8925
rs183036638	snp	C/T	0.0170256	0.0906804	intron-variant	HERC1	GRCh38.p7	15:63747677	ACACATGCACACACG[C/T]GCGCGCACACACACA	8925
rs183040974	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63799668	AAAGAAAAATATAGA[A/C]TTTGAGGAAAAGACA	8925
rs183045246	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63686045	TTTCCTAGACAAAAA[C/T]ATCACACGCTTTGCT	8925
rs183049827	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63706456	TGTAAATAACCCCTT[C/T]CCATCATAATGGAAT	8925
rs183054508	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63665315	AAGGTGGGTGGATCA[C/T]GAAGTCTGGAGTTCG	8925
rs183056717	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63818877	AACCACTTCAGTATT[A/G]CTGCAGCCTACTAGT	8925
rs183062248	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63611414	CTCTAAGCCCTCTTA[C/T]TCCTAAGCCATCTGT	8925
rs183067570	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63690094	CTTGAACCCAGGAGG[C/T]GGAGGCTGCAGTGAG	8925
rs183068744	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63780496	GGAGGCCGAGGTGGG[C/T]GGATCACGAGGTCAG	8925
rs183077224	snp	A/G	0.000196689	0.00991493	intron-variant	HERC1	GRCh38.p7	15:63648227	AAACAAAAGAGTAAG[A/G]AAAAGATAATTATTT	8925
rs183140690	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63819422	AAATAAATGTAAGTT[A/G]TTATTCTCTATTTGC	8925
rs183193408	snp	A/C	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63744295	GACCTAAAGCTAGCA[A/C]AGCACCAGCACAGCA	8925
rs183195356	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63830277	CACCATGTACCCCCA[A/G]TATGATGCATTGAGA	8925
rs183215883	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63710856	ATTCACGCAACAGCT[A/G]AGAGTCCAGTGTGAC	8925
rs183234177	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63702028	TACTTGTCCTTACAA[C/G]TTTGGTTTTTAAATG	8925
rs183247554	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63628117	AAATACCGGCCAGGC[A/G]CTGTGGCTCATGCCT	8925
rs183255288	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63658424	CGTCTAACATCTTTC[A/G]TTCAACAGTACATAT	8925
rs183259646	snp	G/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63784666	AGGCTGGAGTGCAGT[G/T]GCGCAATCTCGGCTC	8925
rs183292772	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63761186	AAATCTACTAGAGAA[C/T]GACCCTCAAACTATC	8925
rs183298238	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63782783	CATCCATGGTTCATG[C/G]GGAAAAGGCCAAAGT	8925
rs183301781	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63738542	TCCTTAAGTCTACAG[A/G]TAGTTCAAATAAAAA	8925
rs183305282	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63779781	AGCACTTTTGGAGGT[C/T]GAGGTGGGAGGATCA	8925
rs183311124	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63716002	GCCCCAGAGGACATA[A/T]TTTGAATGGCCCTAT	8925
rs183313141	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63744054	AGATCTGGGAGAATT[A/C]TCTGGATTATCAGGC	8925
rs183319057	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63671690	TTTAAAAAGTTGCCC[A/G]GGTGGCCTTGGGCAC	8925
rs183322774	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63697075	GGTACATTTATGAAA[A/G]CTAAGACATTAACAT	8925
rs183347780	snp	C/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63626326	ATTTGTGTTGGTTTT[C/T]AAAATGTCTTTATCA	8925
rs183352773	snp	G/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63798649	CCTACAATTATTTAG[G/T]ATTGTCACTCCCCTA	8925
rs183440649	snp	A/G	8.28535e-05	0.00643583	synonymous-codon	HERC1	GRCh38.p7	15:63678000	TATCACAGCCAGCAC[A/G]GGCCACACCTCTATG	8925
rs183458676	snp	A/G	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63789456	AGCAGTATTGACTCT[A/G]GAGTCAAGTAGAATA	8925
rs183464419	snp	A/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63633696	TCAAGACCTAGCATG[A/T]GGGCATTCAAGAATG	8925
rs183466963	snp	A/G	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63612120	TTGAAGCTAGGAAGC[A/G]GAGGTTGCAGTAAGC	8925
rs183473759	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63723034	TTCCACAAAGGGAAA[A/C]ACAAATTGTTTAAAA	8925
rs183483511	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63681291	ACTGAAGCGTCAAAT[C/T]CCTGGGCTCAAGCAA	8925
rs183483792	snp	A/C	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63761568	CACTCTAGCCTGGGC[A/C]ACAGAGCAAGACTGT	8925
rs183492296	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63639522	CCCATCATTAAGTGA[G/T]GCATAGCTACAGTTA	8925
rs183508692	snp	A/C	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63718473	ACATGTATTGAACAT[A/C]TGCAATAACCAAGGC	8925
rs183519177	snp	A/G	0.00122433	0.0247116	synonymous-codon	HERC1	GRCh38.p7	15:63698788	GGGACTTGTAGACAT[A/G]CTTTCCTCTGGCTCT	8925
rs183529759	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63654887	AAAAAAAAAAATTTA[C/T]TATACAACAATCAAT	8925
rs183531390	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63679885	TTCAAATTGCCAGAA[C/T]ATGAAATAGTGCCTT	8925
rs183600314	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63717572	TTAATAAGTAGTTTC[A/G]GCCAGGTGAGGTGGC	8925
rs183605355	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63679161	GCAGAAAGCACCAGG[A/C]CATCATTCGAACCAG	8925
rs183632651	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63633011	GGGAGGGAGTGTGCA[A/G]GGGCAGAGGCAGTTT	8925
rs183639722	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63693538	TGTGAGCCACTGCGC[C/T]TGGCCTGGGGGACAA	8925
rs183652605	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63703245	AAGGGCTTAGACCAA[C/T]TGTGAAACATTAACT	8925
rs183656939	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63724789	AGCAATATATACAAA[A/T]GGGAGATGCTGCAGA	8925
rs183658891	snp	A/G	3.31521e-05	0.00407123	missense	HERC1	GRCh38.p7	15:63675025	AGCACAGAAGCCGTC[A/G]GGCCTCGGAATCGCG	8925
rs183717953	snp	C/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63738935	ACCAGGATATTCCTC[C/T]AACCCCATTTGAGGG	8925
rs183725048	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63808689	GTAATAGATACAATT[A/C]ATCCAGAAATGCAAA	8925
rs183759883	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63650574	AGGCATATGTCACCA[C/T]GCCTGGCTGTCTGTA	8925
rs183761136	snp	C/T	0.000298527	0.0122137	synonymous-codon	HERC1	GRCh38.p7	15:63628735	GTGGCAGCGGCCAGC[C/T]GAGATCTGCCGAACA	8925
rs183777419	snp	C/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63731669	GTGGGCGGGATAGAG[C/G]ACTAAGACTTGTATT	8925
rs183803778	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63687748	TTGAAATTAAAGCAG[A/G]TGACACGACAAAGAG	8925
rs183813645	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63697840	CCTATAGCCTATTTG[A/T]TAGAAGCAAGCCACT	8925
rs183820217	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63809836	AAAAGGGGAAATGAC[A/G]TTTTTTGTTTTCTGC	8925
rs183823479	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63770765	ACTTATAGCTGGGAG[A/G]TAAGTTCTGGCCCAG	8925
rs183845049	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63772658	GGATTTGAATATTGA[A/G]TAAGAAAACACAAAG	8925
rs183846455	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63653932	TACTATTATATCAAA[C/T]CAGCATACAGAGAAA	8925
rs183934888	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63653299	TACAAAAAAATTAGC[C/T]GAGTGTGGTGGTGTA	8925
rs183962458	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63610057	TCCCTCCTTGCAAAC[A/G]TAACTATTTTCTAAA	8925
rs183978098	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63707694	AGCACTTTGGAAAGC[C/T]GAGGCAGGTGGATCG	8925
rs184025776	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63814707	CTCCTGGCCTCAAGT[C/T]ATCTGCCCGCCTCGG	8925
rs184030501	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63817919	AAAAAATGCTGTATG[A/G]GAATTGAATTATCAT	8925
rs184036126	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63748872	CTCATCTACCTGATG[C/G]ACTAAACACGTACAG	8925
rs184049564	snp	C/T	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63790353	GGAGGCCGAGGCGGG[C/T]GGATCACGAGGTCAG	8925
rs184084603	snp	A/G	0.000298348	0.01221	intron-variant	HERC1	GRCh38.p7	15:63641454	TGTATCTCTAGGAGT[A/G]AGTGTAATGAGTTAC	8925
rs184088011	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63617158	AATGCTATCCCTCCC[C/T]GCTCCCCTCACCCCA	8925
rs184110070	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63631837	TGAGCCACGGCGCCC[A/G]GCCCTCCCAAGTCTT	8925
rs184116174	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63767791	GAGCTGAGTATTACA[C/T]GGCAGAACTTTTTTG	8925
rs184137485	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63746078	TACTTGCTTTGGGTT[A/G]AGTTGACTCTTCTTT	8925
rs184137545	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63795148	ATACAAATTATATCA[G/T]TTTTAAATGTATCAA	8925
rs184143792	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63815190	TGGCTCTGATTGTCT[A/G]AAAGTTAAATATGTC	8925
rs184153724	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63727919	ATAAATATTATTTTA[A/G]CTTGGAACTAGAGTA	8925
rs184160001	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63684715	CTAGCGGGGGAAAAA[A/T]ATCTATGTTGGGCCA	8925
rs184160638	snp	C/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63708814	ATTTCAGCTGGAAAA[C/G]CCAAACCATCCCAAG	8925
rs184161650	snp	A/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63776842	TCAGTGAAAGTGCAC[A/T]TGAGATTTTTACATT	8925
rs184175645	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63704297	TTTCTTAGTTGGAAA[A/G]ATGAAGATTCTACTT	8925
rs184176393	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63739994	CAGCTCACCGCAACC[C/T]CTGCCTCCCGGTTTC	8925
rs184201017	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63624674	GCACTCCAGCCTGGG[C/T]ACAGAGTGAGACCCT	8925
rs184271588	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63811259	AGAATGTCCTTCTTC[C/T]TAGAAGATACATGCC	8925
rs184272720	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63791351	AAAATTTTCAGATTT[A/T]TATGTATATATGTAC	8925
rs184284641	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63832394	TATCAAAGAGACATA[C/T]TCATCCCACACTAAT	8925
rs184287644	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63752032	GTGTATACATCAAAT[A/T]CATAAGCATCTTCTA	8925
rs184302830	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63773690	CTAGGATTACAGGTG[C/T]GCACCACCACACCCG	8925
rs184311816	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63762381	CAGGCTGGAGCACAG[A/T]GGCATGATCTCTACT	8925
rs184326420	snp	C/G	0.0150606	0.0854603	intron-variant	HERC1	GRCh38.p7	15:63689310	GAGAAGAAAGTGGCT[C/G]AAACATGCAGATTAC	8925
rs184337681	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63647157	TACTCAGGAGACTGA[A/G]GCAGAAGAATTGCTT	8925
rs184346935	snp	C/T	4.97484e-05	0.00498715	missense	HERC1	GRCh38.p7	15:63616468	TCCCACTGTCTTCAA[C/T]GTGAAGAATGCTGTT	8925
rs184371348	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63758655	CTTAAGAAATAAAGT[A/G]GAAAAAATCACCATG	8925
rs184385181	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63713115	TCACATGCTTTTTCA[C/T]TGCTGTTGTTTATAT	8925
rs184390734	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63822309	ACTTTAAAATAGCCA[A/G]GTGCTGTGGCTCACG	8925
rs184413330	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63803580	GGCGTGAGCCAACAC[A/G]CCCAGCCCCATACTA	8925
rs184427914	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63795886	GAGGAGAATCAAGGA[A/G]GCAGGAAGTTAACTT	8925
rs184435961	snp	G/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63640768	CATTAATACTCCTTT[G/T]CTGCTCCAGGATCCA	8925
rs184496752	snp	C/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63736113	ACAGAAAGGAACAGA[C/G]AAAGGGTAACTGACT	8925
rs184501732	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63683548	CATATTTCTGAGTGG[C/G]TCAATCTGGACTCCA	8925
rs184530817	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63640068	GCCATGCATACCAGC[A/C]AAGACTTATTAGGGG	8925
rs184542515	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63751273	TACCATTATATTACA[A/G]TTTCTGAAGGTATTC	8925
rs184547615	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63820444	TAAATTTTATTAACA[C/T]TGAAATATAATCTTC	8925
rs184556530	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63773151	GATACCGAAAAGACT[A/G]ATCAATGTAGGCCGG	8925
rs184559736	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63708253	AGGCCTCAGAACCAG[A/G]AAAATCTGGTTCTCT	8925
rs184564220	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63731744	AACAATATTAATTGA[C/T]ACACAAACAATTCAA	8925
rs184566539	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63777553	GTTTGTTGGTCATCT[A/G]GATATGCTCTTCTGG	8925
rs184568474	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63688338	TGGGAAAGCCTGGGG[A/G]AAGAAACAGAACGTG	8925
rs184577862	snp	A/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63815587	ATGAAACAATGAACC[A/T]ACATTTGCCTCTGGC	8925
rs184585453	snp	A/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63807475	AGTGTTCCTCTTCTT[A/T]TCCCCTCAGACTTAA	8925
rs184621553	snp	G/T	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63699311	TGCTTAGCTTAAAAT[G/T]CTCTGCAGTATTAAA	8925
rs184655477	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63660484	GGGAAAGGGAGTCAA[C/T]GTAGTTAAATAAGTT	8925
rs184664455	snp	A/C	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63616142	CTCTGTTCACAAACC[A/C]AGCCTGTTGAACTCT	8925
rs184668440	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63691724	TAAAATACCATGTGC[C/T]GTAGAGGATTACATT	8925
rs184673633	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63650278	AGGCATGGTGGCACG[C/T]GCCTGTAGTCCCAGC	8925
rs184683127	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63801840	ATTTTTGGATCCCAG[C/G]AACTCCCAAGGCTTT	8925
rs184687083	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63740768	ATTTTTAAAACTGGG[G/T]TATCTGTCTTTTTTA	8925
rs184691167	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63668603	AGTAAAGACAAACCA[C/T]CCTAACAATTTTTAA	8925
rs184696226	snp	C/T	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63646680	GGGAGTGGTGGCGGG[C/T]GCCTGTAATCCCAGC	8925
rs184697351	snp	G/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63762926	TCTCCTAGGCTCCTA[G/T]TCCCATTATCTCAAG	8925
rs184704007	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63719594	TGGAGAACTGACTTA[C/T]AGGGACAGCAATAGC	8925
rs184723686	snp	C/T	0.0111196	0.0737302	intron-variant	HERC1	GRCh38.p7	15:63826907	ATGCAAATTGGTATA[C/T]TTGTGGAGGAAAATC	8925
rs184752220	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63735504	ACATATGTAACTAAC[A/G]TGCACATTGTGCACA	8925
rs184790559	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63825998	AAACTCCTGACCTCA[A/G]GTGATCCACCCACCT	8925
rs184798655	snp	A/C/G	0.00239393	0.0345281	intron-variant	HERC1	GRCh38.p7	15:63778150	ATTGTAAATAAAAAA[A/C/G]AGAAAAAGTCAACCA	8925
rs184802477	snp	G/T	0	0	intron-variant	HERC1	GRCh38.p7	15:63712660	TCTCTTAAAGTTATT[G/T]TTGAAAAAATTTTTA	8925
rs184803511	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63816863	AATCACTGATGAATT[A/T]AGAAGTCTAAGCAAT	8925
rs184806950	snp	A/G	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63796832	ATAAAGGGTTATGGA[A/G]ACCAAGGTTTTATCA	8925
rs184807896	snp	A/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63674253	TTTTTTTTTTTTTAC[A/T]AATCACTTACAGAAT	8925
rs184811359	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63737495	AGATATATATATATA[C/T]ATATATATATCTTTT	8925
rs184823051	snp	A/T	0.00795532	0.062565	intron-variant	HERC1	GRCh38.p7	15:63758909	CCCCAACTTTTTTTT[A/T]AAATAGATGGGGTCT	8925
rs184826105	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63713152	AAAATTGTGCCTCCT[C/T]ATTTAATCAGAAATT	8925
rs184826905	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63628382	GTGACAGAGCAAGAC[A/T]CCATCTCAAAAAAAA	8925
rs184840243	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63667070	GCCTTATGAAGAAAA[C/T]ACATATGTTAGATAA	8925
rs184851549	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63646056	ACTTAAAAAAATGCA[C/G]CCCTTACATCCCAAT	8925
rs184852605	snp	C/T	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63786934	TATTTTTTTTTTTTT[C/T]ATTTTTTGAGACGGA	8925
rs184860997	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63757444	ATTTTTGTAAATAAT[A/T]TTAGTAGAGACGGGG	8925
rs184865305	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63721840	CTTTGAAAATATGTA[A/C]ATAAAATTAATTTTC	8925
rs184907026	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63780648	AATGGTGTGAACCCG[A/G]GAGGCGGAGGTTACG	8925
rs184914037	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63833763	CGCGCGCACACACAC[A/G]CACACACACACACAC	8925
rs184967500	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63622489	AGGCATGTGCCACCA[C/T]GACCGGCTAATTTTT	8925
rs185013363	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63801082	TCAAGATGCTGGGAG[A/G]GTGGCATGTCAGGAA	8925
rs185021589	snp	C/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63732068	GTGCAGTGGTGCGAC[C/G]TCAGCTCACTTCAGC	8925
rs185038373	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63745448	ATCACTGGGATCAGC[A/G]GTTCCCCTCTGGCTA	8925
rs185040476	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63703544	AAATGCTGTATGAGG[C/G]AAAACATTTTACATT	8925
rs185053042	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63661400	TTAATCAAAAGTCTG[C/T]TTTTTTCATCAGGAA	8925
rs185134008	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63726227	CCTCAGGTGATCCGG[C/T]GGCCTCAGCCTCCCA	8925
rs185167994	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63657155	CTCACTAACAATGTA[C/T]GGGAGTTTTAGCTGT	8925
rs185169524	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63684153	ACACTCTTTAAGAGA[C/T]TGTATTCTCAATACC	8925
rs185172418	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63681124	AACTACTCTCTTGCA[C/T]ATACCTCTGTTTAGA	8925
rs185178127	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63637193	TTAATGAAATACATG[C/T]ATGATTGCTACTGCT	8925
rs185188278	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63790572	GACACAGCAAGACTC[C/T]GTCTCAAAAAAAAAT	8925
rs185194857	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63719961	TGGTATTTGATGCCA[C/T]AAAAGTATATACTGT	8925
rs185197544	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63613930	AATACCCCACCAAAG[C/T]CTGCCAAACGAAAAC	8925
rs185206779	snp	G/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63680418	AAGAACCAGAAAGTA[G/T]TAGAGAGAAAGGAGA	8925
rs185252461	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63763238	GAAACGATAGAATTA[A/G]AATATCATATTTTTG	8925
rs185265261	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63830387	ACCCAAAATGAAAGA[A/C]GTTCTAAAAAATAAC	8925
rs185273850	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63789493	TGCCCACTTGTCACC[A/T]CTATTATCAATAATG	8925
rs185276566	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63816935	TTACATATCTCCCGA[C/T]GGAAACAAAAATCAC	8925
rs185278434	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63770902	TGTAAGAAACATGGG[C/T]TCTAGGCTGGGCACG	8925
rs185297380	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63700154	GAATAATGGTTTTAG[C/T]TGTCGTTGACTTTTA	8925
rs185310026	snp	C/T	0.00597247	0.0543191	intron-variant	HERC1	GRCh38.p7	15:63797055	GGCCATTCAGATGGT[C/T]AGAGAGCTTAGAATT	8925
rs185314923	snp	A/G	0.000124821	0.00789903	intron-variant	HERC1	GRCh38.p7	15:63747678	CACATGCACACACGC[A/G]CGCGCACACACACAC	8925
rs185317539	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63653167	TTAAGTAGGCCAGGT[A/G]CAGTGGCTCACACCT	8925
rs185323517	snp	A/G	1.65638e-05	0.00287778	synonymous-codon	HERC1	GRCh38.p7	15:63677940	GCGCCCAGTTTGCTT[A/G]TGAACACACCGACCT	8925
rs185323644	snp	A/C	0.000552851	0.0166169	intron-variant	HERC1	GRCh38.p7	15:63729195	CAAGTGTTCTTACTT[A/C]TTAATGACTGATTAA	8925
rs185329901	snp	C/T	9.22807e-05	0.00679204	intron-variant	HERC1	GRCh38.p7	15:63656061	AAATAATCAATGTAA[C/T]GGGGAAAAGTACTGA	8925
rs185333460	snp	G/T	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63631575	ATGAAGTTTCGCTCT[G/T]GTCGCCCAGGCTGGA	8925
rs185339628	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63609576	CGCCTGGCACAGGAT[A/G]AGAGTGTAGTAAGAG	8925
rs185360024	snp	A/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63810636	TTGCTTCTTTTTTTT[A/T]ATTTAAAAAAAGGGC	8925
rs185363539	snp	A/C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63808191	AAGCAGCTATAAGCA[A/C/T]ATTTATTATGTTTTT	8925
rs185382101	snp	C/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63781133	AATCACTAATAAAAC[C/T]GTCACAAACAGTTTT	8925
rs185385856	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63827162	GGGTGCAGTGGCTCA[C/T]GCCTATAATCCCAAC	8925
rs185387787	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63715410	TCAACTGCAAAAGTT[C/T]CCTCAGCCTAGGTTT	8925
rs185391460	snp	A/G	0.00108381	0.0232537	intron-variant	HERC1	GRCh38.p7	15:63746873	GCTAAAATCTCAGAG[A/G]AAGACGTGGTTTGAG	8925
rs185397433	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63737912	CTGAAAAATGATTTC[C/T]AATTTAGAATTTTAT	8925
rs185401116	snp	C/T	0	0	intron-variant	HERC1	GRCh38.p7	15:63696543	CAGAATAAAAAAGGT[C/T]AGAGTACAATAGGAA	8925
rs185401352	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63787847	GTGTATGCCTGTGGT[C/T]CCAGCTGGGGAGGCA	8925
rs185405380	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63768483	AATGTGTTGCTACAA[C/T]AACAAATACTTGGTT	8925
rs185411514	snp	A/C	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63812365	TGTATTGTAACATGA[A/C]TGGAGGTAAGTTTTA	8925
rs185430973	snp	C/T	0.000899038	0.0211828	missense	HERC1	GRCh38.p7	15:63706785	TTACACTTACCTCTC[C/T]TTCTGTGAGATGCTG	8925
rs185457704	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63624036	ACACCAGGTACTAAT[A/G]TAAGTACTATTACTA	8925
rs185469753	snp	A/G	0.00165167	0.0286898	intron-variant	HERC1	GRCh38.p7	15:63655733	ATGTTTCAGTAGTAT[A/G]AAACTTACCTTTCTT	8925
rs185493475	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63612907	CCATGTGCTGTCAAA[C/T]TATGCATGTGTGGAC	8925
rs185515763	snp	A/C	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63792351	ATGTTCAACACACAA[A/C]ATTGGTTCTTACTAC	8925
rs185531687	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63833792	ACACACACACACACA[C/G]GACCAGGAGGACGGT	8925
rs185593457	snp	A/C	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63680257	AAGCTTTTATGAGAC[A/C]GAACAAAAGTTACTA	8925
rs185612502	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	HERC1, FBXL22	GRCh38.p7	15:63608376	TCAGAGAGACCCAGG[A/G]TGACAGAAGAACAAT	8925
rs185616997	snp	A/G	3.78888e-05	0.00435235	missense	HERC1	GRCh38.p7	15:63634747	CCTGTCCAATCTGAT[A/G]TCCCTCCAGTGCAGT	8925
rs185627318	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63813787	GAATACAGCATTTTG[C/T]CCAGGTATGGTGGCT	8925
rs185629433	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835898	CAATCAAGAGACTCC[C/G]TCTTTTACCATCTCC	8925
rs185650033	snp	G/T	8.28246e-05	0.00643471	synonymous-codon	HERC1	GRCh38.p7	15:63775036	GCTCACAACTTCAAT[G/T]GCAGTATGAATGACA	8925
rs185668909	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63793861	AAATGAGGCTGAGAC[C/G]TACTGGGCTGCATTC	8925
rs185703495	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63785316	GTGGTCCCAGCAACT[C/T]AGGCTTGGGTGGGAG	8925
rs185727919	snp	C/T	0.0020732	0.0321294	intron-variant	HERC1	GRCh38.p7	15:63694699	GTTAAACACAAAATA[C/T]AGAACATAACTAGTA	8925
rs185730075	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63643239	ATTTTAAAAACACTT[A/G]TCATCAGTAAGAAAA	8925
rs185736189	snp	G/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63618867	TGATACTTTGCTGAA[G/T]TTGCCTATCAGCTTA	8925
rs185738513	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63675355	AAGAATATTCACTAA[C/T]ATATAATGTATGCCA	8925
rs185808151	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63626804	GTACAGTGCAATTCC[C/T]AGATTTATTATTATT	8925
rs185810578	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63742289	CATTCTTTGATTGTA[C/T]ATTGTTGGTGTATAG	8925
rs185816065	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63767406	TATCTACTGGGCAGA[A/T]AAACAATAAATAATA	8925
rs185826371	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63721028	AAGTTTTTATTCACC[C/T]TATATCTAGTTTTTT	8925
rs185827168	snp	A/G	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63806998	TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT	8925
rs185842236	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63700299	TATAACATCCTATTA[C/T]GTGAATATACTACAT	8925
rs185868959	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63690046	GCATGTGCCTATAGT[C/T]CCAGCTACTTGGAGG	8925
rs185919233	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63793669	ATAAACTCACTTTCA[C/G]TTTACTCTGTGGACT	8925
rs185923318	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63774357	TATGAAAATAAGAGG[G/T]TTTTTTTTCTAAAGA	8925
rs185951028	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63710641	CCAGAAAAAACAAAG[C/T]AAGGCAAGGGGGACA	8925
rs185954761	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63753814	TTATAAATTGTGCCA[C/T]CATCAAATAAAAGAA	8925
rs185960730	snp	C/G/T	0.00112857	0.0237285	intron-variant	HERC1	GRCh38.p7	15:63733179	GGAACAAGTAACTAG[C/G/T]GTAATATGCACTAGA	8925
rs185978431	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63685445	GGGATTATATTTCTT[A/G]TGTGTGCACCTTATC	8925
rs185987399	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63641939	CTGCAGAATAAGGCA[C/T]CTACTATATTTCAAA	8925
rs186009499	snp	C/G	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63760716	AAGATCCAACATGCA[C/G]ATAATAGAAATCCCT	8925
rs186012143	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63817447	AGGCCGGGTGTGGTC[A/G]CTCACACCTGTAATC	8925
rs186021274	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63798417	ACCCTCTCCCACCTA[C/G]GTAACAGACACTTAA	8925
rs186034757	snp	A/C	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63824634	GCACCTCTGAGAGAG[A/C]GCTGCACTCCCATGT	8925
rs186084766	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63705238	AGTACCCTGCAACTT[C/T]GAATTCCTGGGCTCC	8925
rs186118398	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63663752	GGCATGAGCCACTGA[C/T]ATAATGTTAATCATA	8925
rs186131063	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63617856	CTTTTTGATGGGGTT[G/T]TTTTTTTCTTGTAAA	8925
rs186139111	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63636602	AAATTGAATTTGTAG[C/G]CATAACCTAGCAAAA	8925
rs186159885	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63779067	GTGTTCAAGGAAGAG[C/T]AGACTCAATGACATA	8925
rs186160913	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63647444	AAAACAGTATGGGGA[C/T]TTCTCAATGAACAAA	8925
rs186175034	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63808979	GATACTTCAAGAACT[C/T]ATTCTTATGGCCTCC	8925
rs186175213	snp	A/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63625298	TTTCTCAGATTAATT[A/T]ATGTAACAACCCTGA	8925
rs186179432	snp	C/T	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63778490	AGAGGAAAGAAAAAG[C/T]AAAAAGGAAGAGAGA	8925
rs186236651	snp	A/G	0.00305478	0.0389623	synonymous-codon	HERC1	GRCh38.p7	15:63689637	CTGAATAGCATGTTT[A/G]GCCTGAGCAATGGGT	8925
rs186244864	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63670159	TAATGGTTTACAGGC[A/G]AGTTATGGAAAGAAA	8925
rs186251848	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63613292	AATTCTACCCTGCTC[C/T]GTTCTCTTAGCATCA	8925
rs186286625	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63804152	AATGATTCACAGACC[A/G]AAACGTAAGAGCTAA	8925
rs186294645	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63823945	AGGAACTCACACAAC[A/G]CAATAGCAAAAAACA	8925
rs186300792	snp	C/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63743299	ATGGAGTCTCACTCT[C/G]TCACCAGGCTGGAGT	8925
rs186303140	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63782767	TAGATGCCATTAAGA[A/G]CATCCATGGTTCATG	8925
rs186310989	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63737660	GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCT	8925
rs186314209	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63764737	AGTGATGGTCAGGCA[A/G]TGGTTAACTGTCTCT	8925
rs186319144	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63695688	CCACCACGCCCGGCC[A/G]AGTCTGTATAATCTA	8925
rs186337893	snp	C/G	0.00874735	0.0655527	intron-variant	HERC1	GRCh38.p7	15:63759941	CAGTCCCTAATAAAA[C/G]GTCTGGAATTTTGCT	8925
rs186346518	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63652605	TTATTATTTGAAAAA[A/G]TTGTATCCAATTTTT	8925
rs186395167	snp	G/T	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63828517	GCTAATTTTGTATTT[G/T]TAGTAGAGATGGGGT	8925
rs186404292	snp	A/C	0.00676609	0.0577691	intron-variant	HERC1	GRCh38.p7	15:63722395	CAAAGGGAAGATAAT[A/C]GTTAAACAGACTCTT	8925
rs186411243	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63664841	TGTTTAATGAAGCTC[A/C]AATTTAAATGAGATC	8925
rs186419568	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63630920	TAAGAGGCTTCTCCA[A/G]TATCCACATCTTTGA	8925
rs186478978	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63755067	ATTTAAATATCAGCA[C/T]TAAAATCTAGGTCTT	8925
rs186485028	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63711217	GTAATCTCAGCTACT[C/T]GGGAGGCTGAGGCAG	8925
rs186485098	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63781874	AATCGCCTTTTTCCT[C/G]ATATGGGGAAAGTCT	8925
rs186489952	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63671811	ACTAAGGAAAGAGGG[C/G]AAAGAAGAAAAAGGG	8925
rs186504006	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63713956	TCAGTTATTTTCAAC[G/T]TACGGTCCCAGACCA	8925
rs186514490	snp	G/T	0	0	intron-variant	HERC1	GRCh38.p7	15:63676278	GAAAGGTCGACACTT[G/T]CATGTCATTCTGTAA	8925
rs186521568	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63823008	TCATACCTTCTGTGT[C/T]GTACAAATTTAGTTT	8925
rs186569390	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63818315	TGCATAAAGCACTCC[A/G]GCTCACTGAGCTCCC	8925
rs186571407	snp	C/T	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63828956	TACAGGTTAGCAATC[C/T]GTAACCACTTCATGT	8925
rs186605036	snp	C/G	0.00716266	0.059414	intron-variant	HERC1	GRCh38.p7	15:63771802	GTATGGCTTTAGAGA[C/G]GAAGGAGGGAGGAAC	8925
rs186609958	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63809674	AAGGACATTTAGAAG[A/G]TATACTCAGCAGGAC	8925
rs186610181	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63762545	GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG	8925
rs186610416	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63718986	GTCATCCAACACCTG[A/T]ATTTTATCATCTTTC	8925
rs186611432	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63790250	ATTGCTATCTCTACC[A/T]CCAATATTGGTTGTA	8925
rs186614242	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63740332	TCATTTGTTTATCAG[C/T]TGACAGACACATGTT	8925
rs186619441	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63629742	GAGTCAAACTGAGGC[C/T]AATATGAATAATGCT	8925
rs186664736	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63733255	ACTAGCTTAATAAAT[A/C]ATCATCTTCAGGAAG	8925
rs186664925	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63763674	AGTGGTCAAAGTCAC[A/C]ATAGTGGTTACTTTG	8925
rs186679252	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63804713	CATATCCAATGAGAC[A/G]TGTATCAAGAATATA	8925
rs186703679	snp	C/G/T	1.66924e-05	0.00288893	synonymous-codon, missense	HERC1	GRCh38.p7	15:63698977	GTCACTCAGGGATTC[C/G/T]AATTGACTGTGCATA	8925
rs186704086	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63690414	ATAAAGAAAGCAGTC[C/T]TAAAAGTAAACGTTA	8925
rs186715198	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63679981	GTCAAGTACTTTTAA[C/T]GGCAGAAGAAATAGC	8925
rs186716387	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63648727	AAACAGTATCTGTGA[G/T]GGTAGAATGGGAGTG	8925
rs186746867	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63803891	TAAAACTAGTAACTA[C/G]TAATCAAGACGTGGT	8925
rs186774937	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63647832	GTTGGCAAGAAAGTG[A/G]TGAAAAGGGAACTCA	8925
rs186837013	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63765696	CCCACCTCGAGTTAT[A/C]CCATCCTTTCAGATC	8925
rs186839095	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63652023	CCTAGGCAGCAGAGC[A/G]AGACTCAGTCTCAAA	8925
rs186901156	snp	A/C	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63782910	GGTGGAAATAGCAAG[A/C]GAAGTAGAATTAGAA	8925
rs186961970	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63686089	TAGAAGAAAATGTGT[C/T]CTGTGTGACTCCTTA	8925
rs186969222	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63633162	TTTATGGGCGACAAT[A/G]ACTGCTTTATATGTT	8925
rs186982959	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63611712	ATTTAGGGAAGGTTG[C/T]TGGTTGTAGTATGCT	8925
rs186987408	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63665455	GGGAACTGCTTGAAC[C/T]GGGGAGGCGGAGGTT	8925
rs186995409	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63643856	AATACTGACTACTTT[C/T]TAACCAGTGTTTTGA	8925
rs187002405	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63625872	GTTATCTTATTAGCC[A/G]TGAAAGAATTTTCCA	8925
rs187032399	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63812880	CGAAGACTAAATATT[A/G]TAAAATGTCAACTGT	8925
rs187032616	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63811198	AGGTGACAATGAATT[A/C]ATGTTATTTTCCATC	8925
rs187072211	snp	C/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63819100	CAATCACTTACTTTA[C/G]AGATCAAACCTGCAG	8925
rs187103466	snp	A/C	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63683122	GCCTGGGCAACAGAG[A/C]TACACTCTGTCTCAA	8925
rs187111872	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63703030	AATTGCTTGAACAGG[A/G]ACCCGTGAGGAGGAG	8925
rs187112125	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63660021	TTCTGAAAATACATC[C/T]AAAATGCAGATGAGC	8925
rs187139908	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63639864	ATATACAACTAAAGC[A/C]CTAACAAAGTACCTA	8925
rs187145899	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63701271	GAGGTAGTCTTACAT[A/C]TTCATTATTAACCAA	8925
rs187155091	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63774010	TTCCTCTGACAACAC[A/G]CTCTTCACAGATCTT	8925
rs187157402	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63732290	ACAGGCATAAGACAC[C/T]GCGCCTGGCCTGAAG	8925
rs187171623	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63657764	TGATTTATTTTTCTT[C/T]TATATTTAGATCTAA	8925
rs187178837	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63615226	TGAAAACAGTCTCAA[C/T]CCAACCAAAGACCAA	8925
rs187184081	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63766372	GTGGGCAGATCACTT[C/G]AGGTCAGGAGTTCAA	8925
rs187187282	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63724369	TTCACCAGCCATGGC[C/T]AAAATCACTTTCTGG	8925
rs187191699	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63744414	AAAGCCAGCCAGGCC[A/G]TGTCCTTCCCTTCAG	8925
rs187197335	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63795236	AACTGGGTCAATTGT[C/T]TTAGTTACTAAAGCT	8925
rs187210997	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63815272	CGCTCTCCACCTTCC[A/G]TATCTTGCAATATAG	8925
rs187312563	snp	G/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63747144	CTGTGCTATCCAGTT[G/T]GGGTAACATTTTTAT	8925
rs187351892	snp	C/T	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63706274	TATAATATCTCTTCA[C/T]GTAAGAGATAAAGCA	8925
rs187356650	snp	G/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63681224	AATTTTCTAAAGAGA[G/T]GGGGTCTCACTCTGT	8925
rs187363629	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63752760	CTCCACTAAGATTTA[C/T]CTGGGTCACATATGC	8925
rs187369453	snp	C/T	0	0	intron-variant	HERC1	GRCh38.p7	15:63658881	GAGAAACTCACATAT[C/T]TCTAAGTTTGAACTT	8925
rs187371122	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63639524	CATCATTAAGTGATG[A/C]ATAGCTACAGTTACA	8925
rs187375017	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63710021	TGCTTTAGCAAAGGC[C/T]CAAGAGGTATGCTTG	8925
rs187380276	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63638041	GGTTTGGCGCTATAT[C/T]GTACCAGGATTATTA	8925
rs187392951	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63615487	TGGTGACACATGCCT[A/G]TAGTCCCAGCTACTG	8925
rs187409390	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63788093	AGAATAGCTACAATA[C/T]ATAAAGACATTTGTA	8925
rs187414271	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63827863	CCTTGACAAAATTAT[A/G]CTAAGTGAAAGAAGC	8925
rs187436039	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63815078	CATCTAATCTACCTC[C/T]CCTAGAAGTATACCT	8925
rs187443924	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63794783	GTTTAAGAAAAACAC[A/G]TAAAGGGTTCAGTGG	8925
rs187459256	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63756927	GCCTTTTCATGCTCA[C/T]AACTTTGTTGCTGAG	8925
rs187467138	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63734928	TAAAGCGAACTCACT[A/G]ACTACTAGGATCATG	8925
rs187474867	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63776469	TCATAAAACGAAACA[C/T]ATATCTAACCCTATG	8925
rs187513609	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63664449	CTTTCACAAAGAAAA[A/G]GATACGGAACATAAA	8925
rs187536919	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63801123	AACTCCATGCCCCTA[A/C]CCCCTGTATCTTGCC	8925
rs187552051	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63745107	TCCCCTATCCTGCTG[C/T]GACCAAGATGTTATC	8925
rs187557463	snp	A/C	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63712198	ATGTGGAAGGTGGGC[A/C]CAAGGCAAGAGGTGA	8925
rs187581238	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63691338	GGGAGTGGTGGTGCA[C/T]GCCTGTGATCCCAGC	8925
rs187591751	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63729425	TCAAGGTGTAAAAAT[A/G]TCATGGCCTATCCAA	8925
rs187592036	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63770056	CTTCACATTACATAT[A/G]GGATCAAGTCCCCAA	8925
rs187603435	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63825597	ACTTTTGTGGGCTTA[C/T]TTTGTAATCAGTAAA	8925
rs187626048	snp	C/T	0.00597247	0.0543191	intron-variant	HERC1	GRCh38.p7	15:63785241	CCAGCCTGAGCAACA[C/T]AGCAAGACATTACCT	8925
rs187626980	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63685892	CTGGCTTATTGTATC[C/T]AGATTGTACAAACAA	8925
rs187633968	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63767026	TTTTTTTTTGAAATG[G/T]AGTCTTGCTCTGTTG	8925
rs187637874	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63730903	ATTTAGAAAATATCA[A/C]AACTCTATTTTAAAA	8925
rs187638439	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63806668	GTCTAACAAGTCTAC[A/G]GAGAAATAACAAAAT	8925
rs187668393	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63686858	TAATGTTCAAAAGGA[C/G]ATGACTTCTAAGTTG	8925
rs187672609	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63808551	TCAGCCTCCCAAAGT[A/G]CTGGAATTACAGGCG	8925
rs187677295	snp	C/G/T	8.28046e-05	0.00643399	missense	HERC1	GRCh38.p7	15:63645065	GTATCTTGAGGAATG[C/G/T]GCCAAACACATACTA	8925
rs187730788	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63690861	TTTATGTATACATAA[A/T]GGGAAGAGCATTGTA	8925
rs187733957	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63711528	ACAATGAAACGTAAA[C/G]ACACTGTTCAACTTT	8925
rs187775863	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63780662	GGGAGGCGGAGGTTA[C/T]GGTGAGCCAAGATCG	8925
rs187783877	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63819930	AAATAAGGTTTTACC[C/T]CATAAGTTTAAACGT	8925
rs187803278	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63739145	AAAGCCGTGTGCCCA[C/T]TACCAGTCATTCCTT	8925
rs187808151	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63698405	CCTGGGCAACGAGAG[C/T]GAAACTCCGTCTCCA	8925
rs187856567	snp	A/G			missense	HERC1	GRCh38.p7	15:63672539	GGGACTCGGATGCAG[A/G]CACTGTTTCTGTGTC	8925
rs187862487	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63649295	GAGTCAGAGGTTGCA[C/G]TGAGCCGAGATCGCG	8925
rs187866725	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63627638	GAGATTGCGCCATTA[C/T]ACTCCAGCCTGGGCA	8925
rs187868251	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63780497	GAGGCCGAGGTGGGC[A/G]GATCACGAGGTCAGG	8925
rs187869200	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63621990	CTTCTTCTCTCAACT[C/T]GTCAAAGTCATTCTC	8925
rs187931566	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63748017	GATTACCTGAGGTGA[G/T]GAGTTCAAGACCAGC	8925
rs187933766	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63707187	TGAAGTAGTGCCTTA[C/T]TTTCCAAAATTACTA	8925
rs187940173	snp	A/G/T	6.62728e-05	0.00575609	missense	HERC1	GRCh38.p7	15:63654211	TAGTTTGGTTGTCAC[A/G/T]GTCGTGTGCAGCAAG	8925
rs187961447	snp	A/G	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63665680	TCCTTTTTCAGTACA[A/G]TTTTACACAAAAATT	8925
rs187962658	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63621489	GGAGTTGCTCTTCTC[A/G]AGGAGTATCTCTGTG	8925
rs187995024	snp	A/G	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63667585	TATTATGGAGCTTAT[A/G]TGTAAAAGTGAAATG	8925
rs188001046	snp	A/C/G/T	9.93768e-05	0.00704843	synonymous-codon	HERC1	GRCh38.p7	15:63716354	TTCATCCTCTGGCTC[A/C/G/T]GGATGCCCCTCTTCC	8925
rs188006635	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63646100	GAGAATCTGGGATAT[A/G]TTTTGTGTTTATATG	8925
rs188016276	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63697119	TCAACTAAACCTAAA[A/G]TAAAATAGTATTAAT	8925
rs188020528	snp	G/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63623111	AGAACCAAAAGGAAT[G/T]AGAAAGTCAATCCAG	8925
rs188052784	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63798930	ACCATCAGGTTTGGG[A/G]GTGTCCCAATTCCAA	8925
rs188065121	snp	A/G	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63761339	AATACCAGTACTTTG[A/G]GAGCCCGAGGTAGAA	8925
rs188078991	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63738849	ATTTTATTCTAGTAC[C/T]TTTACCCTTTTCAAA	8925
rs188080697	snp	A/C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63687997	TTATCCAAAGAATGA[A/C/T]GAGAAACCATTGGAG	8925
rs188080963	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63780107	ATTGCATTAGATTTA[G/T]GTACTTTCAGAAAAT	8925
rs188084569	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63761973	AGCTCTGTCTACCAT[C/G]AATATAAAAACCTAG	8925
rs188084724	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63707794	GTTAGCTGGGTGTGG[C/T]AGCACACGCCTGTAA	8925
rs188111195	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63679619	GTTTACAATGGAGGG[C/T]ATCCTATTAATACTG	8925
rs188132994	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63784770	CTGCCACCGCATCCA[A/G]CTAATTTTTTTTGTA	8925
rs188136205	snp	A/C	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63830713	CTTTTCTGTAAGTCT[A/C]ACATTATTTCTAAAT	8925
rs188140214	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63800494	GTCACAAGATATCAG[C/T]TTAAACAGTACAGTA	8925
rs188144597	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63825336	GAGCAATATAATTAA[C/T]ATTAGCATATTATAT	8925
rs188150210	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63758120	TATTTAATGCAAATA[A/G]GCATGAATATACACC	8925
rs188220199	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63655304	GGTTGTACTGAGCCA[A/G]GATTGTGCCACTGCA	8925
rs188238959	snp	A/C	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63633748	TCATTATGAACTACC[A/C]AAAGTACTAAAGGTA	8925
rs188246355	snp	C/T	0	0	missense	HERC1	GRCh38.p7	15:63612259	TACTTACCCTATCAA[C/T]CTTCATGATTTGAAA	8925
rs188273151	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63791372	ATATATGTACGTATA[C/T]ATATATTACAAATAC	8925
rs188278916	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63782075	TCCACAACATAAAAG[C/T]GCAAGGTGAAGCAGC	8925
rs188280884	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63811592	AGACGGGCAGATCAC[A/G]AGGTCGGGAGATCGA	8925
rs188361202	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63736037	CAGGGGTTGGTGGGA[G/T]AAGTCAAAAAGACCC	8925
rs188404892	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63615971	GTAGAAATGACAGCA[A/G]AAAGTATTTTACATA	8925
rs188412137	snp	A/G	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63808244	TGATTCTGAATAACG[A/G]CTGCTATCAAACTTG	8925
rs188414183	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63787857	GTGGTCCCAGCTGGG[A/G]AGGCATACTGGGGAG	8925
rs188428800	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63776873	TCACTGCATGTAAAT[C/T]TTGCCTCAACAAATA	8925
rs188432738	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63735798	ATTGAAAAATTCAAG[C/T]ACACAAGAAGAATAA	8925
rs188437905	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63723450	TGATTATGAAATGAT[A/T]AACTTCAAACCATTT	8925
rs188439347	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63805832	TCTGTGGTCCTAGCT[A/G]CTTGGGAAGCTGAGG	8925
rs188453018	snp	A/G	2.15399e-05	0.00328169	synonymous-codon	HERC1	GRCh38.p7	15:63649885	TGGCCAAGCCAGGGC[A/G]GATACCCAATGAGGC	8925
rs188474906	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63682008	AGTGAATCTCTGAAT[G/T]TGAGGGTGGTCTTGG	8925
rs188480508	snp	A/G	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63708502	AATCCTGCCAGAAAC[A/G]AGGGAGCTAGGGAAT	8925
rs188492549	snp	A/T	8.47824e-05	0.0065103	intron-variant	HERC1	GRCh38.p7	15:63680528	ATGCTTGTGAATGGG[A/T]GTCGGTACCTCTCCA	8925
rs188494698	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63688508	CTTAAATGAGTCTGA[A/G]TAAGGTTTCTTTGAG	8925
rs188498894	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63656721	GGCTTTTCTCAGTCA[C/T]GATGCTCTCAGAAGT	8925
rs188502928	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63636659	TGATGACAAGGAAAA[C/T]GAGGATGACAGCAAT	8925
rs188508864	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63613563	AGTAACTATGTGAGG[C/T]GATGGATATGTTAAT	8925
rs188515240	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63668725	TATTCATTAAAAGAA[C/T]GTAAGAATCCTAAAT	8925
rs188560259	snp	A/G	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63751329	TGTAACCTAGGAGCA[A/G]TAGGCTATACCATAT	8925
rs188578418	snp	A/G	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63773273	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAGTA	8925
rs188591816	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63703323	TTAGTATCCCCACTG[C/T]CAAATACTGAGATTA	8925
rs188600212	snp	A/T	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63775972	GAACCTGGGAGGCGG[A/T]GGTTGCAGTGAGCCG	8925
rs188610380	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63734178	TCTCCAAAAAAAGAT[C/T]TAAAAAGAAAGAAAA	8925
rs188624310	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63660764	TATTCTGTGGTAAAG[C/T]TGGTCTTTGAAACCA	8925
rs188660968	snp	G/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63628401	TCTCAAAAAAAAACT[G/T]AGTTGCTGCTAAAAT	8925
rs188663979	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63814148	GGAAAAGAGTATTTC[C/T]GTATATAAATAGACC	8925
rs188710644	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63744067	TTCTCTGGATTATCA[G/T]GCAGAGACTCTTGTT	8925
rs188710697	snp	A/G	0.0126979	0.078662	intron-variant	HERC1	GRCh38.p7	15:63746137	TTACTGATTCGATAT[A/G]TATTTTTTTTAATAT	8925
rs188719244	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63787045	TGGAGTTTCACCATG[C/T]TGGCCAGGCTGGTCT	8925
rs188725027	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63768002	ATAGTCTCCGTTATC[A/G]CCCCACCCCATTAAT	8925
rs188736640	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63616168	ACTCTCGTGACCTCA[C/G]GCCTCCCCTTCCACC	8925
rs188738192	snp	C/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63702117	GTAGGCAAGCTAAAA[C/G]GGGAAAAAAATTAAA	8925
rs188741855	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63674044	ACTATGTATTTTGAG[C/T]CAGATCAATAAATAC	8925
rs188748147	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63628262	CCAGGAATGGTAGTG[C/T]ATGCCTGTAGTCCCA	8925
rs188805187	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63830341	AAACATGCTTAACCT[C/T]AATCAAATCATGAGA	8925
rs188832550	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63728879	CCAAAGAAAGAATTT[A/C]AAGAAGGAAAGTGAA	8925
rs188840964	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63684760	CACCTGTAATCCCAG[C/T]ACTTTGGGAAGCCAA	8925
rs188845056	snp	A/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63704934	TAGTAGAGACAGGGT[A/T]TCACCATGTTAGCCA	8925
rs188854274	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63759421	TGCCTGCCAAAAGCA[C/T]AGGACCCAGAGTGGC	8925
rs188858348	snp	A/G	0.000587989	0.0171362	intron-variant	HERC1	GRCh38.p7	15:63713307	AGTGCATAAAGTAAT[A/G]AAGGGAAGTGAGTAG	8925
rs188859251	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63662195	CAGATAACACAATCG[A/G]AAGGTGTTCTTTGCC	8925
rs188866233	snp	G/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63755724	AAATCAAAGATGCAG[G/T]GGGCTGAGATAGCAC	8925
rs188870301	snp	C/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63794012	CTGCGATGGCCATGA[C/G]AGTGACCTCTGGTTG	8925
rs188878690	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63725217	CAGTTCTCTATTTAG[C/T]AAATCAGAATAGAGA	8925
rs188884518	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63684121	GAGTGTGTTTTCTGG[A/G]GGCAATATACTTCCA	8925
rs188892151	snp	A/G	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63678670	GACTGACTCAATTTA[A/G]TCTAAAATAAGCCTT	8925
rs188900219	snp	A/C/G	0.000315578	0.0125576	synonymous-codon	HERC1	GRCh38.p7	15:63640407	CAAGCATTGCATATA[A/C/G]GGGCTATGAACAAGT	8925
rs188914953	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63631842	CACGGCGCCCGGCCC[C/T]CCCAAGTCTTATTCC	8925
rs188918140	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63778186	GGGTACATGCTTTCA[C/G]CTCCATCCAGCCATA	8925
rs188929645	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63816881	AAGTCTAAGCAATTA[C/T]CATCAACAGCTGCTA	8925
rs188935928	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63796938	TTCTATCAGTAATTC[C/T]AAAAGAGAGGAGGGT	8925
rs188936353	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63749976	CCTTTAGGCATTCAC[C/T]GTATAGGCAGAAAAA	8925
rs188939538	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63790375	CGAGGTCAGGAGATC[A/G]AGACCAACCTGGCTA	8925
rs189087851	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63732212	CACCATATCGGCCAG[C/G]CTGGTCTCAAACTCC	8925
rs189088271	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63773842	GAGACACCGCACCCA[C/G]CCTAAATTTGTATTT	8925
rs189088480	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63810119	ATGATTACTATGATA[A/T]ACTAAGTTAAAAATA	8925
rs189117315	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63689350	AAGCTTAGTACTACA[A/G]GACAAGAGAGAAGAC	8925
rs189126158	snp	C/T	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63661405	CAAAAGTCTGTTTTT[C/T]TCATCAGGAAAAAGA	8925
rs189128515	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63684176	TCAATACCCTCTAGG[C/T]GATGTCCCAACATGT	8925
rs189129160	snp	A/G/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63803902	ACTAGTAATCAAGAC[A/G/T]TGGTAGTGGCAACAA	8925
rs189133669	snp	G/T	0.000399281	0.0141238	missense	HERC1	GRCh38.p7	15:63694468	TTTAGCAGACCAGTG[G/T]AAATTGCCAAAGAAA	8925
rs189146115	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63640774	TACTCCTTTTCTGCT[C/T]CAGGATCCAATCTAA	8925
rs189150579	snp	A/C	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63616844	ACTAAAAATTCAGTT[A/C]TTCGGCTTCCCTAAT	8925
rs189151680	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63650990	TACATCTCCCCAAAC[C/T]CTACTCTGAATACTT	8925
rs189155802	snp	G/T	0.00216606	0.032838	missense	HERC1	GRCh38.p7	15:63675109	CTAGGCGACCAAAAA[G/T]TTGGGAAGCTTTAAT	8925
rs189168131	snp	A/C	0.00874735	0.0655527	intron-variant	HERC1	GRCh38.p7	15:63629013	TGGAGTGCAGTGGCA[A/C]AATCTCAGCTCACTG	8925
rs189182570	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63653824	TGGATGCAGAACCCA[C/T]GGATACAGAGGATCA	8925
rs189202963	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63611112	TGAAGAAGGACTTAC[A/T]AAAGCAGAGGGAACA	8925
rs189207952	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63772988	GAAAATAAATTCAAC[A/G]TAATTGGATTTTATG	8925
rs189220484	snp	A/C	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63713137	TGTTTATATATACGA[A/C]AAATTGTGCCTCCTC	8925
rs189226698	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63736826	TGGGCAGGCTGGTCT[C/T]GAACTCCTGACCTCA	8925
rs189233984	snp	A/G	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63647169	TGAGGCAGAAGAATT[A/G]CTTGAACCTGGGGGT	8925
rs189237719	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63731680	AGAGCACTAAGACTT[A/G]TATTGGAAGAAAAAG	8925
rs189331788	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63820591	AAGGTCTTAAAATAC[A/G]GCAAAACTTTAAAAA	8925
rs189338513	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63769003	ATTTAACAATACCAA[A/G]CCAACAAAATATCCC	8925
rs189349981	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63780959	AGTAAATCATTTTTT[A/T]AATGTATATCCTAAG	8925
rs189358637	snp	A/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63752402	CTATCCTCAACAAAC[A/T]AATAGGGTAAGAGTG	8925
rs189359389	snp	C/T	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63762942	TCCCATTATCTCAAG[C/T]AGCAGAACATGTTCC	8925
rs189367942	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63732502	GAATTTAAGAAACAC[C/T]AGAGATTTAGAATTA	8925
rs189370299	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63801853	AGCAACTCCCAAGGC[G/T]TTTACCTATCTCATA	8925
rs189389413	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63708895	CCAGGTCTCCCTTCA[C/T]CTGAAATGGAATCTG	8925
rs189399678	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63669772	CACAATCTTCTTATA[C/G]AAGAATATGCAACCT	8925
rs189413010	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63823434	TATTCCCATTTTATA[G/T]ATCAGAAAACTGAGA	8925
rs189420352	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63624590	CTCCCAGTTACTCAG[C/G]AGGCTGAGGTGGGTG	8925
rs189444876	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63781484	TGATTGTTATTATTG[C/T]AATTGTTTGGGGGTG	8925
rs189455104	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63741773	GTTTTGGCACTCTTG[C/T]AGAAAATCAGTAAGC	8925
rs189463242	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63700215	GGACACACTCTTTCA[G/T]TCAATATAATATTGC	8925
rs189475904	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63740924	AATGTTTTTAATTTT[A/G]ATGATGTCCAATTTA	8925
rs189477731	snp	A/C	0.000399281	0.0141238	missense	HERC1	GRCh38.p7	15:63689645	CATGTTTGGCCTGAG[A/C]AATGGGTGTCTCCCA	8925
rs189480119	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63710089	CCACTGCAGAAGAAT[A/G]CTGGTTCCAAAAGCA	8925
rs189494327	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63670510	TTTTCCTCTACTAAA[C/T]GATGTTCGCCCAGTA	8925
rs189498612	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63647522	CCAAAGGAAAATAAT[G/T]CATTTTCTCAAAAAG	8925
rs189519815	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63625137	ATGCACACACACACA[C/T]GCACGCACACACAAT	8925
rs189553073	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63813806	GGTATGGTGGCTCGC[A/G]CCTGTAATCCCAGCA	8925
rs189591930	snp	C/G	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63826990	GCAATCACACTTACA[C/G]AAATCTACCTTGAAG	8925
rs189683904	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63646699	TGTAATCCCAGCTAC[C/T]CAGGAGGCTGAGGCA	8925
rs189703422	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63763265	TTTGCAACAAAGCAC[A/G]AAAGAATTAATATAG	8925
rs189714861	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63803599	AGCCCCATACTAACT[G/T]TTTAGAAATTAAAAC	8925
rs189721259	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63720353	TTTCAAATGGGGGTG[A/G]GAGAGTTATTGTCCA	8925
rs189747463	snp	A/G			upstream-variant-2KB	HERC1	GRCh38.p7	15:63835747	CCACCATATTGGCCA[A/G]GCTGGTCTCGAACTC	8925
rs189753690	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63722017	AGGCACACGCCTCCA[C/T]GACCAGCTAATATTT	8925
rs189774357	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63657527	GAATTCTTTACACAT[G/T]CTGTTGGTTAGATGC	8925
rs189774887	snp	A/C	5.15159e-05	0.00507497	intron-variant	HERC1	GRCh38.p7	15:63712746	CTTGAAAACAAAAAT[A/C]TTTCTTTACTGAATC	8925
rs189778380	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63627016	GATTCAGCCCCAGCA[A/G]TGTGGCCCCAGAGCT	8925
rs189782928	snp	A/T	1.66045e-05	0.00288132	missense	HERC1	GRCh38.p7	15:63674382	GTCTTCCAAAAGCCC[A/T]TGAACCACTAATTTA	8925
rs189784908	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63641809	TGGAACTTCAAAATA[A/T]CCTAAATTTTGTCTA	8925
rs189786806	snp	A/C	0.0287284	0.116357	intron-variant	HERC1	GRCh38.p7	15:63637773	TTACTGAAAGGGAAG[A/C]GTTGATATAACTATG	8925
rs189826209	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63763849	ACTTAATACAACATT[C/T]TTTCAATTAAAGTTA	8925
rs189829870	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63809728	GTGTAGTTTTAATCA[A/G]GAAACAAAGTACTGT	8925
rs189836720	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63742359	GCTGAACTCGTTTAT[C/T]AGCCCTAATAGTTGT	8925
rs189853728	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63807725	CCCAACTGTCTCTGC[C/T]CTAGTCAGGTAGGAA	8925
rs189889553	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63829670	TAAACATACCGAGTA[C/T]ACAGATTTTGATTTT	8925
rs189895972	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63767443	AATAAAAACAGCAAA[C/T]ATCCCCAGCACTTTG	8925
rs189917463	snp	A/G	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63726266	GGATTATAGGCATGA[A/G]CCATCATGCCGGGCC	8925
rs189919645	snp	C/T	0.00597247	0.0543191	intron-variant	HERC1	GRCh38.p7	15:63695264	CGGGTTTTAAACTCC[C/T]GAGCTCAAGCAATCC	8925
rs189927541	snp	A/C	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63652065	CAAAACAAAACAAAA[A/C]AAACTGTTGAAAATG	8925
rs189955854	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63650335	GCCGAGATCACGCCA[C/T]TGCACTCCAGCCTGA	8925
rs189969036	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63702336	ATACATGTTATACCA[C/T]GAAACACACATGTTG	8925
rs189970091	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63807032	ATTACAGGCATGAGC[C/T]ACCACACCCGGCCTG	8925
rs189974349	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63761030	GTAACATATTTAAGA[C/T]AGACAAGAAGAAAAG	8925
rs189975239	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63753985	TCGAGGCCAGCCTGG[A/G]CAATAAAGCAAAATC	8925
rs189977000	snp	A/C	0.00755907	0.0610114	intron-variant	HERC1	GRCh38.p7	15:63659097	ATTCCCTATACCAAA[A/C]ATTTACCACACCCTC	8925
rs189977180	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63710826	TTAAGGCCCTAAAGG[G/T]AACTTGTGTTGCAGA	8925
rs189979164	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63682165	GTGGCTATGGAGTTA[C/T]ACATAGTATGAAACA	8925
rs189983533	snp	C/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63733224	GATCCCAGAAAAAAA[C/G]TATACTAATCCACTT	8925
rs189995664	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63639620	CATAAATCTTAAGTA[C/T]ACAAAGAGGTTGTTA	8925
rs189997840	snp	A/C	0.000399281	0.0141238	synonymous-codon	HERC1	GRCh38.p7	15:63615903	ACTCTGGCCAACAAA[A/C]GAATCAAGAGGAATC	8925
rs190022503	snp	C/T	0.0166325	0.0896639	intron-variant	HERC1	GRCh38.p7	15:63692902	TCCCAAATATCAGGA[C/T]AGGCGCAATGGCTCA	8925
rs190037656	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63617460	TATGAATAGTGCCGC[A/C]ATAAACATACGTGTG	8925
rs190055144	snp	C/T	0.000798403	0.0199641	downstream-variant-500B, intron-variant	HERC1, FBXL22	GRCh38.p7	15:63608155	TGGCTGCCCTCCCCA[C/T]TGAGACATGTTGTAA	8925
rs190112589	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63822751	AAGAGACTATTATAA[C/T]TACCCACACAGGAGA	8925
rs190119831	snp	A/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63706970	CAAGTCAAACTAATA[A/T]CAAAATGTCCCTAAA	8925
rs190128079	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63730571	CTATAAAGGACATTA[C/T]AGGGGCAACTGTAGA	8925
rs190131085	snp	A/G	0.0142736	0.0832652	intron-variant	HERC1	GRCh38.p7	15:63686237	TTTATATTATCTTAC[A/G]TAATAATAGAACATT	8925
rs190161676	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63785331	TAGGCTTGGGTGGGA[A/G]GATCGCTTGAGCTCA	8925
rs190163285	snp	A/C	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63828760	GAACCCAAAATGGAA[A/C]AGTAACAATAACAAA	8925
rs190170479	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63675689	CCTCTATAGTTTAAG[C/T]CAAAATATAATTATA	8925
rs190180094	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63745650	GAGTGGCACTGCCTA[C/T]TCAGGACTGTTTTTT	8925
rs190183382	snp	A/G	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63789943	GATGAAGATCACACA[A/G]ACAATATTAGAGGAA	8925
rs190187779	snp	A/G	0.00795532	0.062565	intron-variant	HERC1	GRCh38.p7	15:63703674	GGGTGGACTGCTTGA[A/G]CCCAGTTCAAGACCA	8925
rs190188326	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63817020	TTTACAGGAAATTCA[A/G]GAGACAGGAAGAACA	8925
rs190190197	snp	G/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63771462	TTTTGAGACAGTCTT[G/T]GTCTGTCACCCAGGC	8925
rs190194222	snp	A/T	0.0410537	0.137264	intron-variant	HERC1	GRCh38.p7	15:63809523	TCAGGAGCTGTGGAT[A/T]ACACTAAGATAATGA	8925
rs190220172	snp	A/G	0.00676609	0.0577691	intron-variant	HERC1	GRCh38.p7	15:63826060	TGAGCCACCACGCCC[A/G]GCCAAATAATAATTT	8925
rs190240303	snp	C/T	0.000399281	0.0141238	synonymous-codon	HERC1	GRCh38.p7	15:63746942	TTCATCTGGGACAGT[C/T]GAGTCCATCAGTCTG	8925
rs190248622	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63777655	AGTCTGTCCTCAACA[C/T]TGCAAATATTTCTTC	8925
rs190250339	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63815731	CTCTAACCTAACATG[C/T]TAGTCCGGTCTCATG	8925
rs190290963	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63629935	GAATACATCAACCTC[C/T]TGAGTCTCTTATCAG	8925
rs190385958	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63793095	GCCCAGGGCTTTCAC[A/G]CCCTCTCTGGGGATG	8925
rs190403224	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63685906	CTAGATTGTACAAAC[A/C]ATATGGTTTATGCTA	8925
rs190405957	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63706355	TTTTTATTTCAACGT[C/G]TGTGTACACGTGTAC	8925
rs190412704	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63630981	CCCTCAAGTTTCTTA[C/T]GTTCTTTTTTGAGAC	8925
rs190413762	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63665022	AAGCCTTGGTTACTA[C/T]ATGGCTCCATAGTTA	8925
rs190415359	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63652797	GCTGGATTACAGGCA[C/T]GTGCCACCACAACTG	8925
rs190426110	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63643602	GATAAATTATATAAG[C/T]TCAAGATTTATCATT	8925
rs190428949	snp	A/C	0.000798403	0.0199641	utr-variant-3-prime	HERC1, FBXL22	GRCh38.p7	15:63608705	AATATATGAATATTC[A/C]TGTAAAACTGTCCTT	8925
rs190434109	snp	A/G	0.000501136	0.0158214	intron-variant	HERC1	GRCh38.p7	15:63752903	AAGTATTACTTTTTA[A/G]TCACCTAATCCTCTG	8925
rs190466842	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834735	TAGGTCCAAGTGGAC[A/T]TTAAATTGTTGAGTG	8925
rs190476107	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63799255	TCTGTAATCACAGCA[C/T]TTTGGGAAGCTGAGG	8925
rs190486376	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63818740	AGAAATGGGACATAC[G/T]AAACTTTTATCAACA	8925
rs190490573	snp	A/G	0.0126979	0.078662	intron-variant	HERC1	GRCh38.p7	15:63795952	AAGGAAGAGGAACAG[A/G]CTACGACCTAATGCT	8925
rs190492055	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63635546	GTGCTATACAATCTT[A/G]CAATATGATTTTAGA	8925
rs190498906	snp	C/T	0.000399281	0.0141238	synonymous-codon	HERC1	GRCh38.p7	15:63729348	AAGATGTTTATGAAG[C/T]AATGCCACACTGCTT	8925
rs190530149	snp	C/T	0.00636936	0.0560724	intron-variant	HERC1	GRCh38.p7	15:63758739	CCAGAATTGTTCATA[C/T]ACAAATTATTTAACA	8925
rs190556261	snp	A/C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63719724	ATTTTGAAGGCAGAA[A/C/T]TGACAGAATTTGTTG	8925
rs190562191	snp	C/G	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63680276	CAAAAGTTACTAGAT[C/G]AAATTCTCAATTAAC	8925
rs190597865	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835364	GAGTAGCTACATGAG[A/G]AGTGATGTCATTGTT	8925
rs190604524	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63738886	CACTACCCCGTTTCT[A/G]ATAAATATTAAATCA	8925
rs190610784	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63761392	TAAGACCAGTCTGGG[A/C]AACCATAGCAATACC	8925
rs190630220	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63774602	TCACCAAAAGTCTCA[A/T]ATCATTCACTATTAC	8925
rs190638278	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63813078	ACATAAATGAAACAT[A/G]TTGCCAATCCTCAAA	8925
rs190642339	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63793800	AAGTTCCCTGTGTTA[C/G]AGATGTGTGAACCAA	8925
rs190647180	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63774033	CAGATCTTTCCTTAG[C/T]TCATCACTTCCCTTC	8925
rs190692083	snp	A/G	0.000133185	0.00815932	synonymous-codon	HERC1	GRCh38.p7	15:63690601	CACAGCTTCAAGGAC[A/G]TGAAGTGCAAGGAGC	8925
rs190696191	snp	G/T	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63649158	AGGAGATCGAGACCA[G/T]CCTGGCCAACATGGT	8925
rs190733516	snp	C/T	0.00081152	0.0201271	synonymous-codon	HERC1	GRCh38.p7	15:63775513	AACCAGTTTAGAATA[C/T]AGAACAGCAACTCCC	8925
rs190742735	snp	C/T	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63613034	TTTTGTAAAAATTAT[C/T]TGTGCTCATCGTAAA	8925
rs190762238	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63733417	AATGATTTTAGTACT[A/G]TAAGTAGAGAGGAGT	8925
rs190819961	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63699328	TCTGCAGTATTAAAC[C/T]AGATCATCATTTATG	8925
rs190834165	snp	A/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63614413	TATCAATACATTTCT[A/T]GTCAGTTATTTATTC	8925
rs190834623	snp	C/T	0.00132887	0.0257424	intron-variant	HERC1	GRCh38.p7	15:63655982	ATTGGAAAAACAGAC[C/T]TAATTTTTACATGTA	8925
rs190883032	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63817672	GTCAGCCAAGTTCGC[A/G]CCACTACACTCCAGT	8925
rs190888009	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63715939	GGCATAGAAAGGGGC[C/T]CTCTTCCTCACCGCT	8925
rs190895867	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63738026	TCTCTCAGAAGCTAC[C/T]GATGGATGAAGAAAC	8925
rs190906212	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63696765	AACTATAAGGTAGTA[A/C]TGCTACTGCTTTCTT	8925
rs190911904	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63653295	AAAATACAAAAAAAT[A/T]AGCCGAGTGTGGTGG	8925
rs190913998	snp	G/T	1.6571e-05	0.0028784	missense	HERC1	GRCh38.p7	15:63677996	CTCCTATCACAGCCA[G/T]CACGGGCCACACCTC	8925
rs190923856	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63779302	ATCAACTCCAAGAAA[C/T]AGCCTAGAAAAACTA	8925
rs190934844	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63671872	TTAAGTCATAGTTAA[A/G]AGAGCTCATAAAACA	8925
rs190935644	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63631832	AGGTGTGAGCCACGG[C/T]GCCCGGCCCTCCCAA	8925
rs190991166	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63755577	TGAGCTCAGGAGTTC[A/G]AGTTCAGCCTGGGCA	8925
rs190991795	snp	C/T	1.91415e-05	0.0030936	synonymous-codon	HERC1	GRCh38.p7	15:63626060	GTAGAGCAGCCGGAG[C/T]CTGGCCCGCACCGTG	8925
rs191002137	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63793913	AGCCACAGGATGAGA[C/T]AGGAGGTCAGCACAA	8925
rs191022744	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63711267	GAGTTCGAGGCTGCA[C/T]TGAGCAGCCTGAACT	8925
rs191050591	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63782768	AGATGCCATTAAGAG[C/T]ATCCATGGTTCATGG	8925
rs191058383	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63765046	AAAAATTAAGCTGAC[A/G]GCTGACTTATGCAAG	8925
rs191069930	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63625713	AAAAAAAAAAAAAGA[A/C]AGAAATGGTATGTGT	8925
rs191073481	snp	C/T	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63671426	CTATTATTCCTCTAT[C/T]TTCCTTATTCTTTGA	8925
rs191108548	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63804323	GGGCACAGTGGCTCA[C/T]GCCTGTAATCCCAGC	8925
rs191114850	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63755843	AAAAAGAGAAGATAT[A/G]AGCTCAGTTTCTTAT	8925
rs191117360	snp	A/C	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63784953	TTTAAAGAAATCCAA[A/C]ACAAGGCAAAACCTA	8925
rs191123293	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63766543	CAGATCGCACCACTG[A/C]ACTCCAGCCTAGGTG	8925
rs191130513	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63824025	TCTCCAAATAGGACA[C/T]AAAAATGCCTCAACA	8925
rs191131698	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63806339	CACTTTTCCTTCAAA[G/T]GCCTATCTCAAAGGT	8925
rs191134212	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63798622	TCTCTAACAGGATAC[C/T]TCTCACTTTGACCTA	8925
rs191190618	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63760223	GACTTTTTTTTAACA[C/T]TACACACAAAAAAAA	8925
rs191228528	snp	C/T	0.000399281	0.0141238	missense	HERC1	GRCh38.p7	15:63644993	CACCAGAATGTTACC[C/T]GGCAATTTGATTCCT	8925
rs191231952	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63821724	AGAGTGATACCCTGT[C/G]TCAAAAAAAAAAAAA	8925
rs191234531	snp	C/T	0.0205511	0.0992634	intron-variant	HERC1	GRCh38.p7	15:63714637	TCACTGCAACCTCCA[C/T]CCCCAGGTTCAAGCG	8925
rs191245446	snp	A/C/T	0.000132596	0.00814137	synonymous-codon	HERC1	GRCh38.p7	15:63675024	CAGCACAGAAGCCGT[A/C/T]AGGCCTCGGAATCGC	8925
rs191251477	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63724430	TATTTGGAAATGGAG[A/G]AAAATCCTCAACTGC	8925
rs191253512	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63744622	GCCTCGCCCCATAGC[C/T]ACCACCACCCCAGGC	8925
rs191261772	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63683202	AAGCTTGTAACTTCA[C/T]AAATGCTAAAGTTTC	8925
rs191263852	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63628570	TGGCAGAAGGCTTGA[C/T]GGTTTCACAACGATG	8925
rs191265965	snp	A/C	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63650362	CTGAATGACAGAGCA[A/C]GACTCCGTCTCAAAA	8925
rs191267861	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63703242	ACCAAGGGCTTAGAC[C/T]AATTGTGAAACATTA	8925
rs191310273	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63690056	ATAGTCCCAGCTACT[C/T]GGAGGCTAAGGCAGG	8925
rs191320138	snp	G/T	3.25335e-05	0.00403308	intron-variant	HERC1	GRCh38.p7	15:63648223	ATCAAAACAAAAGAG[G/T]AAGGAAAAGATAATT	8925
rs191335844	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63676849	TCACAATGGGCAGCA[C/T]AATGAACAGTTACAT	8925
rs191381142	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63740404	ATTCATGTACAAGTT[C/T]TTGTGTGGACATATG	8925
rs191395246	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63762723	AAGAGCAGATAGAAA[G/T]AATCAAGCATTTATT	8925
rs191404108	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63790274	GGTTGTAGAAATGGA[A/G]ATGTATGTAAAAGTA	8925
rs191410508	snp	A/G	0.00501975	0.0498465	intron-variant	HERC1	GRCh38.p7	15:63680072	AAGGTTTGAGACTTC[A/G]TTACCTTTTCCCCTG	8925
rs191412492	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63699124	CATGTTTGAATACGC[A/G]CATGCATTAAGTGAA	8925
rs191420557	snp	A/C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63655667	ATAATTTATCATATA[A/C/T]TAACAATGTAAAAAC	8925
rs191423562	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63778828	CTGATGACGACAAAG[C/T]AAAGTGTAAGTTAAC	8925
rs191452883	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63737760	GAGAACACAAAGGAC[A/G]AGAAGAACTTGCTAT	8925
rs191458522	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63780663	GGAGGCGGAGGTTAC[A/G]GTGAGCCAAGATCGT	8925
rs191463634	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63695877	TTGGATCTATTCCCA[C/T]CCAAACTGGATAATA	8925
rs191469610	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63665549	AGAAAAAAAAAAGTT[C/T]AATTCTATCAAATAC	8925
rs191549540	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63808604	CAATATACTTTTTAA[C/T]GAAAGGATCTTTGGG	8925
rs191568270	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63770239	CCTCACAATTGCTGG[C/T]AAAACCCTCCTACTT	8925
rs191576240	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63697621	CACCACGCCCAGTTA[A/T]TTTTTGTATTTTTAG	8925
rs191697410	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63783274	TCTTGTTTTAATAAA[C/T]TGCCAAAGTAATCCC	8925
rs191704351	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63824949	GCTAGGAGAGTAGGG[A/G]AGATGCAGGTCAAGG	8925
rs191705778	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63679833	AACTAGGTCTTGTAG[G/T]TCTTGTGACTGCACG	8925
rs191713296	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63654444	AAGCAAATGGGTTAA[C/T]CCATATCTTTTAAGA	8925
rs191714593	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63633431	GACTCAGATTTCCTT[C/T]GTATTGTTTTCTTAA	8925
rs191715763	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63744227	ACCTAAAGCTGGGGG[C/T]GGAGTGACACAAGCA	8925
rs191718488	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63811258	GAGAATGTCCTTCTT[C/T]TTAGAAGATACATGC	8925
rs191722642	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63790753	CACTTGTTAAATGCT[A/G]GCAGAAGAAACACAG	8925
rs191723539	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63611823	ATCTGGAAATTCTAA[C/G]TATTAATAAGCATGA	8925
rs191735639	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63831932	CAAATGAATGGATGT[A/G]TCACATGCAAACAGC	8925
rs191792377	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63663995	TATATTTTACATGCC[C/T]AGAACGTAATCCTAG	8925
rs191792691	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63788391	GATTTAAAGAAACTA[C/T]AATCACAACAAAATA	8925
rs191802195	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63618805	GCTCTCTGTCTGTTA[G/T]TGGTGTATAAGAATG	8925
rs191806941	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63828281	GTAGAAACAAAGATG[A/G]AGGGATGGAAATGAG	8925
rs191821633	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63717228	CATGTCATTTATCCC[A/C]ATATATGAGTTTCAA	8925
rs191829123	snp	A/G	0.00716266	0.059414	intron-variant	HERC1	GRCh38.p7	15:63751578	AGACTGGACCATACT[A/G]TATAGTATGGTGGGA	8925
rs191840428	snp	A/G	0.0197687	0.0974348	intron-variant	HERC1	GRCh38.p7	15:63773380	ACCCAGGAGGCAGAG[A/G]TTGCAGTGAGTGGAG	8925
rs191848253	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63708571	ACACCTGTCAAACAG[C/T]TAAACTTAGGGTTGG	8925
rs191850411	snp	C/T	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63747374	CTGAGGCAAGAGAAT[C/T]ACTTGAACCTGGGAG	8925
rs191851252	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63731933	GTGTACAATGTACAA[A/T]TCTGGAAAAGGATGA	8925
rs191863768	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63705601	AGCTATTAAGAGAAG[A/G]GTTTCATTCTGAAAT	8925
rs191895695	snp	C/T	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63802933	ATAAAATAGGGGCTG[C/T]GTGTGGTGGCTCATG	8925
rs191967540	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63821894	ATGGAGTTTACATTC[A/T]AGTAAGGAAGACAAA	8925
rs191992887	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63722622	ACCCTCTTGGTTTTA[C/T]GATCTACTGCTGCGG	8925
rs191996037	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63681227	TTTCTAAAGAGATGG[A/G]GTCTCACTCTGTTTC	8925
rs192002537	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63804985	AGAACTCTCATACAC[A/T]GCTGGTAGAAATGTG	8925
rs192022485	snp	C/T	0	0	intron-variant	HERC1	GRCh38.p7	15:63723679	ACTAAATGTCCTACA[C/T]GTGCAATGGTCTTGT	8925
rs192027178	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63765707	TTATCCCATCCTTTC[A/G]GATCAAACCAATAAG	8925
rs192038816	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63794528	GTGACCAGCCCCAAT[C/T]CTGAAGCTAACCAGA	8925
rs192094188	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63639345	GCCTAGAGCATTGAA[C/T]ACAGTCATATTCTGT	8925
rs192094693	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63609782	GCGCCATGGCTGCCT[C/T]GCACAGCTCACATAA	8925
rs192096406	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63642154	ATCAAATCAGCACAT[C/T]GGCTCTAATCTTTAA	8925
rs192114590	snp	A/C	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63731705	AAAAAGAGTACGTAG[A/C]CCAGACCCTGAAGAG	8925
rs192124942	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63688019	CCATTGGAGTATTTT[A/G]AGCAGGGGATGAACA	8925
rs192130788	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63707824	ATCCCAGCTACTTGG[A/G]AGGCTAAGGCAGGAG	8925
rs192133145	snp	C/T	0.00636936	0.0560724	intron-variant	HERC1	GRCh38.p7	15:63668027	GTTGGTGCTGCAATC[C/T]CTGCAATGTTCAAGG	8925
rs192147519	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63646491	AGTATCAAGCAATAG[C/T]AGAGGCTAAAAAAAA	8925
rs192153020	snp	A/G	1.66551e-05	0.00288571	intron-variant	HERC1	GRCh38.p7	15:63623687	AAATGGCCACTAGCA[A/G]ACTAGATAACTCAGC	8925
rs192157136	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63815341	GCTACCTAGGTTTAG[A/G]TCCTGGCTTTGCTAT	8925
rs192172525	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63777236	TCTAAATATAAAATC[G/T]GATGACACTTGCCTT	8925
rs192176256	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63735977	CTAAGGATTAAGAAC[C/T]AAATGCACATATTCT	8925
rs192185199	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63685613	GTTGTAACTGGCTAA[A/G]TCTAGGACCCCTAAA	8925
rs192231642	snp	A/C	0.00676609	0.0577691	intron-variant	HERC1	GRCh38.p7	15:63615987	AAAGTATTTTACATA[A/C]AAATACGGCACAGCA	8925
rs192262964	snp	A/C	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63757408	CATGAGATTATAGGC[A/C]CGCGCCATCATGCCC	8925
rs192266889	snp	C/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63727374	ACTTGGACTAAGTGA[C/G]ACTTGATCACTGAAC	8925
rs192272170	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63693275	TTGAGACAGGCTCTC[A/G]CTCTGTCATCCAGGC	8925
rs192274665	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63735137	TGGGTGCAGAAATGA[A/G]TAAGACAGACAAAAT	8925
rs192276242	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63776830	AAATAAAAAAACTCA[C/G]TGAAAGTGCACTTGA	8925
rs192298287	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63743871	GTGGATGCCAGTAGA[C/T]ATTGAAGAGTTAGGT	8925
rs192319994	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63660442	ACTTAACCAAACTGC[A/G]CTCCTGAAGCATAAG	8925
rs192331631	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63815101	GTATACCTTGTTTTA[C/T]GGATAATGGTTCCCA	8925
rs192336463	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63794996	GTTTGAACCTGGGAG[A/G]CGGGGGTTGCAGTTA	8925
rs192347135	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63814332	GTTAAAATGCAACTT[C/T]TCTTTGTGACCCAAA	8925
rs192400762	snp	A/C/T	0.018221	0.0938453	intron-variant	HERC1	GRCh38.p7	15:63775986	GAGGTTGCAGTGAGC[A/C/T]GAGATCGCGCCACTG	8925
rs192417137	snp	C/T	0.0138799	0.0821421	intron-variant	HERC1	GRCh38.p7	15:63622352	TTTTTTTTTGAGATG[C/T]GGTCTCGCTCTGTTG	8925
rs192460087	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63748141	TAAGGCAGGGGAATC[A/G]CTTGAACCTGGGAAG	8925
rs192461770	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63707666	GGGAGTGGTGGCTCA[C/T]ACCTGTAATCCCAGC	8925
rs192468277	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63658141	GTATTTCTGGTTCTC[A/G]TCCCCTTTTTACATT	8925
rs192485158	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63615228	AAAACAGTCTCAATC[C/T]AACCAAAGACCAATT	8925
rs192515239	snp	A/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63819932	ATAAGGTTTTACCCC[A/T]TAAGTTTAAACGTGC	8925
rs192516147	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63795524	TCAAATAGAAAAGCT[C/G]TGATACAAAAGGTTC	8925
rs192520514	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63711571	AATCCTTTATGGAAG[C/T]TTTTTTAAAACAATA	8925
rs192522773	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63825351	TATTAGCATATTATA[C/T]ACCAGAAATTTTCTA	8925
rs192526843	snp	C/T	0.000933107	0.0215797	synonymous-codon	HERC1	GRCh38.p7	15:63734790	ATGAAGTAATTCCAT[C/T]CGTTCTCGTAATGGA	8925
rs192528848	snp	A/G	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63691226	ATCCCAGCACTTTGG[A/G]AGGCTGAGGCGGGCA	8925
rs192547384	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63672878	CTTTGTATTCACTAC[C/T]GTACTCATTAATTCC	8925
rs192553502	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63649309	AGTGAGCCGAGATCG[C/T]GCCACTGCACTTCAG	8925
rs192556769	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63627784	ATGGAAGATAGATCA[A/G]ATCAGAAAGGGCCCA	8925
rs192571107	snp	C/T	0.00676609	0.0577691	intron-variant	HERC1	GRCh38.p7	15:63806901	TACAGGCATGCGCCA[C/T]CGCGCCCGGCTAAGT	8925
rs192575466	snp	G/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63785301	TGGTGGTACACGACT[G/T]TGGTCCCAGCAACTT	8925
rs192585217	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63628371	CTCCAGCCTAGGTGA[C/T]AGAGCAAGACTCCAT	8925
rs192637313	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63639905	AAAATGAGAAAATAT[G/T]GGACTATGTCATTGA	8925
rs192688196	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63712998	ATACACACACAGGGA[G/T]GAGTAATGTCAGTTG	8925
rs192733585	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63800741	ACATACTTGGTGTTC[A/G]TAATTTCCTTTGTGA	8925
rs192749505	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63718314	GGAATAATCATTCAT[A/G]TGATTTGAATCATTC	8925
rs192751680	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63762365	TTTTGGTCTTATTGC[G/T]CAGGCTGGAGCACAG	8925
rs192753704	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63689037	AAGGATCAAACTCTG[C/T]GGAACACCAACATTT	8925
rs192767333	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63772351	TGTTCAAACACACCA[C/T]TGGCAAACATTTAAT	8925
rs192778581	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63731023	ATATTTTTCATAATA[C/T]TGTACTGCATATTCT	8925
rs192808757	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63810270	GCAGAAATAGACCAA[C/T]TGTCCATCAACAGAT	8925
rs192812360	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63801766	GTGGTACCACAGTGG[A/T]TATATCCTAGGGATT	8925
rs192817064	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63773012	TTTTATGAGACACTC[C/T]TGTCCAAAAGCTTTC	8925
rs192840076	snp	A/G	0.00192985	0.0310033	intron-variant	HERC1	GRCh38.p7	15:63649932	CTTTTCCTCCTAAAA[A/G]GGAAAAAATGTTAAC	8925
rs192859547	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63653830	CAGAACCCACGGATA[C/T]AGAGGATCAAATGCA	8925
rs192863508	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63611283	AGGCAGCTAAGGTCA[C/T]TGGCATTTATTTCGG	8925
rs192915258	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63698623	TACAGGAAAGGGGAA[A/G]GCAAGGAATAGAAGA	8925
rs192917180	snp	C/T	0.000314635	0.0125387	missense	HERC1	GRCh38.p7	15:63669634	TTGGTAACGAAGATA[C/T]TGGAGGAGTCTGTGC	8925
rs192943478	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63780517	ACGAGGTCAGGAGAT[G/T]GAGACCATCCTGGCT	8925
rs192944544	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63819202	GGTTGCAGAACCAGA[A/T]CCAGTTCATTTCTGG	8925
rs192960918	snp	A/G	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63739324	TGCCTCAGCCTCCCA[A/G]GCGGCTAGGACTACA	8925
rs192967499	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63712393	AGATAAGAAAAAAGA[A/G]TCAAGGATGATCCCA	8925
rs192973789	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63674179	CTAATAGAAAAATAA[C/T]AAAAAAGAACTGTTT	8925
rs192979869	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63826307	AGAACTTTAAACTCG[C/T]GGTTTAATTTTCATT	8925
rs192995370	snp	A/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63746023	TTTTCTGTTCTTTAT[A/T]TTTTTAATTTCACTC	8925
rs193000389	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63786797	TTTACTTTGGAATTA[C/T]GAAAATGTTTTGGAA	8925
rs193026931	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63634289	ATCTAAGGAATGATA[C/T]AGAAAAAGCCAAAAA	8925
rs193027837	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63751060	AGGAACTAAAGATAA[C/T]GACAGTGAAATAATG	8925
rs193030023	snp	A/G	0.00953873	0.0683987	intron-variant	HERC1	GRCh38.p7	15:63790455	AGTGGCGGGCGCCTT[A/G]TAGTCCCAGCTACTT	8925
rs193030354	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63666710	TATGTAAATAACCCA[C/T]TCCTCATCCAAGTTC	8925
rs193067530	snp	A/G	0.000369891	0.0135944	intron-variant	HERC1	GRCh38.p7	15:63632560	ACATGAAAGAGAAGT[A/G]GAAAATTATCTATAC	8925
rs193099942	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63684126	TGTTTTCTGGGGGCA[A/G]TATACTTCCAAACAC	8925
rs193102888	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63640650	AACTTTATCCAATGT[A/T]AACATCTTATACAAC	8925
rs193113695	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63767163	ACGCCACCATGCTTA[A/G]CTAATTTTTTTGTAT	8925
rs193124520	snp	G/T	0.000182184	0.00954248	missense	HERC1	GRCh38.p7	15:63725480	GCTGGCTGAGGTAAT[G/T]GCAGACCAGCAGGAT	8925
rs193152745	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63678889	TTTAATCATTCTAAG[G/T]CTTAGCTTTTCATTT	8925
rs193190416	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63691698	AAAAGTATATTGAGC[A/G]TGTAAACATATAAAA	8925
rs193193587	snp	C/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63807294	ACTTCCAGTTGCATT[C/G]GGCCATTGAGAGGCA	8925
rs193198341	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63767645	GGAGGCTGCAGTCAG[C/T]CGAGATCGCCCCACC	8925
rs193218139	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63687442	ACTTAGGAAGCTGAG[A/G]CAGAAGAATCGCTTG	8925
rs193220665	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63612687	CTTGTTTCTCAGACC[G/T]CCAGGCACGAGAGTC	8925
rs193222322	snp	A/C	7.12073e-05	0.00596646	intron-variant	HERC1	GRCh38.p7	15:63645706	GGAAGGAAGAGAAAA[A/C]AAATCAGAGTAATGT	8925
rs193258409	snp	C/T	0.000298295	0.0122089	synonymous-codon	HERC1	GRCh38.p7	15:63660980	CAAACTACCTTCATA[C/T]ACACTGTCTTGCTTG	8925
rs193260190	snp	A/C/T	0.000101494	0.00712306	intron-variant	HERC1	GRCh38.p7	15:63616411	ACACCAGTAGAAACA[A/C/T]AGACTGGCCAGGATT	8925
rs193276051	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63745116	CTGCTGTGACCAAGA[A/T]GTTATCTAAGACACA	8925
rs193276591	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63703521	AGACCACTGAGACTA[A/G]TAAATGCAAATGCTG	8925
rs199512402	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63683482	GGCTAACGAGTTCTT[A/G]TAAAATCATATGTCT	8925
rs199521087	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63780837	AAGACTGATGTGAAA[C/T]AATAATAACCTATAT	8925
rs199544390	snp	A/G	6.81419e-05	0.00583664	missense	HERC1	GRCh38.p7	15:63626109	AGCGCCCCATACTGG[A/G]GGGGCACTGTGTCAG	8925
rs199555951	snp	A/G	0.000199235	0.00997887	intron-variant	HERC1	GRCh38.p7	15:63628635	CCATGGGGTACTGCT[A/G]AAAAAGAAACGCTGC	8925
rs199563151	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63779416	GGCATTATTTTAAAA[G/T]AAAATAGCACAGCCA	8925
rs199583046	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63748976	CAAAAAAAAAAAAAA[A/T]TTCAAAAACCAACCA	8925
rs199600997	snp	C/G	0.00011137	0.0074614	missense	HERC1	GRCh38.p7	15:63672580	GTGGTGGCAGTTGTG[C/G]TGTCCTCCAGAGAGC	8925
rs199602197	snp	A/C	4.96956e-05	0.00498451	synonymous-codon	HERC1	GRCh38.p7	15:63713496	CACGGAGTTGCATGC[A/C]GCAGTGTACACATCC	8925
rs199635033	snp	C/G/T	0.00134507	0.0258987	missense, synonymous-codon	HERC1	GRCh38.p7	15:63674748	TTTCCCTTCTGTTAT[C/G/T]TGATGTTGGGATTCC	8925
rs199643850	in-del	-/AT			intron-variant	HERC1	GRCh38.p7	15:63829512	TATACACACACACAC[-/AT]ATATAAATAATATGT	8925
rs199654305	snp	C/T	1.66679e-05	0.00288681	missense	HERC1	GRCh38.p7	15:63756580	GACCATCAGATCCTT[C/T]AGAAGATGAAACCTT	8925
rs199679380	snp	A/G	0.00217219	0.0328843	intron-variant	HERC1	GRCh38.p7	15:63656062	AATAATCAATGTAAC[A/G]GGGAAAAGTACTGAA	8925
rs199683306	snp	A/G	0.000467864	0.0152877	missense	HERC1	GRCh38.p7	15:63633855	GTACTGACCTGAGGT[A/G]AAGATTTTGCAGTGG	8925
rs199687563	in-del	-/CACT	0.0681886	0.171594	intron-variant	HERC1	GRCh38.p7	15:63614075	CAGTTATGGGATAAA[-/CACT]CAGTTCTAAGAGATG	8925
rs199690859	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63831645	ATATACCCAGCCCCC[-/T]TTTTTTTCTATTTCA	8925
rs199746656	snp	A/T	0.0287284	0.116357	intron-variant	HERC1	GRCh38.p7	15:63619829	TGTATTTCTGTGGGA[A/T]CGGTGGTGATATCCC	8925
rs199749335	in-del	-/TTTTC	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63741604	GCGCCTGGCCCTATG[-/TTTTC]TTTTATGAGTTTTAC	8925
rs199771827	snp	C/T	0.000117005	0.0076478	missense	HERC1	GRCh38.p7	15:63694391	GGGAAACACCCGTCT[C/T]TGGCAACAACTGCAG	8925
rs199774775	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63657830	GGTTGGGACCAAGGC[-/T]TTTTTTTTTCTATGT	8925
rs199804379	snp	C/T	1.65644e-05	0.00287783	synonymous-codon	HERC1	GRCh38.p7	15:63716348	CTCCTCTTCATCCTC[C/T]GGCTCCGGATGCCCC	8925
rs199811363	snp	C/T	8.50015e-05	0.00651871	intron-variant	HERC1	GRCh38.p7	15:63634727	TCTTATTGATTTATT[C/T]CATGCCTGTCCAATC	8925
rs199828316	snp	A/T	0.00337466	0.0409382	intron-variant	HERC1	GRCh38.p7	15:63656378	CAGTAAAGAAAAACA[A/T]CTCAGATGGATAAAG	8925
rs199829930	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63784486	TTTTTTTAAAACCTA[A/G]GAACACTAGTTGCCT	8925
rs199840315	snp	C/G	4.05729e-05	0.00450386	missense	HERC1	GRCh38.p7	15:63654316	GGGCATTAGCCAACT[C/G]CAGAGGGCCTACAGC	8925
rs199840935	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63688435	GTAGAAGATGGGAAT[A/C]TAAGTCTAGAATTCA	8925
rs199848862	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63651969	TGAACCCAGGAGGCA[C/G]AGGTTGTGGTGAGCT	8925
rs199857083	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63805948	ACCCTATCTCAAAAC[A/C]AAAAAAAAAAAACAA	8925
rs199876597	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63706960	ATTCATCATTCAAGT[C/G]AAACTAATAACAAAA	8925
rs199927270	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63760120	GGGCAGAAAAAAAAA[-/T]TGAACTGGATAGGGA	8925
rs199934275	snp	A/G	0.000133563	0.00817089	synonymous-codon	HERC1	GRCh38.p7	15:63658705	GGAGCTCTTTTCTAC[A/G]GAGCCATGGCAACCT	8925
rs199937922	snp	A/C	0.000302539	0.0122954	intron-variant	HERC1	GRCh38.p7	15:63612220	AGCAATAAGGCAGAC[A/C]TTACAAAGGAAAAAA	8925
rs199971171	in-del	-/TA	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63682137	AGGAAAAGATAAAAC[-/TA]TCTGGTACCTAGGTG	8925
rs199983480	snp	A/G	4.9586e-05	0.00497901	synonymous-codon	HERC1	GRCh38.p7	15:63764126	TAATGCTGCCTCGTA[A/G]AGGGAGCACAAGCCA	8925
rs199985740	snp	C/T	0.000216405	0.0103998	missense	HERC1	GRCh38.p7	15:63678241	GTCCAACGGTCTGTT[C/T]GGTGAAGGATACGGA	8925
rs199988730	in-del	-/T	0.0345262	0.126772	intron-variant	HERC1	GRCh38.p7	15:63807052	ACCCGGCCTGAGTGA[-/T]TTTTTTTAAGGCTCA	8925
rs200009446	snp	A/T	3.01237e-05	0.00388084	intron-variant, missense	HERC1	GRCh38.p7	15:63713686	ACATGCAACACAAAA[A/T]CAAGGTCTTAACACA	8925
rs200023211	snp	C/T	0.000108958	0.00738019	missense	HERC1	GRCh38.p7	15:63656089	TGAAAGTAGCTTACC[C/T]GTGTACACAACTGTA	8925
rs200026752	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63701818	AGGAAAGAACTTTAA[-/T]TTTTTTTTTAAGTAT	8925
rs200039834	in-del	-/TTTC			intron-variant	HERC1	GRCh38.p7	15:63693238	TTGGTGCTGGGGAAT[-/TTTC]TTTTTCTTTTTTTTT	8925
rs200044650	in-del	-/TTTCA	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63766999	AAAGTTTTATAGGTT[-/TTTCA]TTTGTTTTTTTTTTT	8925
rs200067991	snp	A/C/T	0.000111555	0.00746775	intron-variant	HERC1	GRCh38.p7	15:63725260	AGGTACAAACAGGCA[A/C/T]GTATTTTAAATGCTG	8925
rs200074092	snp	A/G	8.80088e-05	0.006633	intron-variant	HERC1	GRCh38.p7	15:63645714	GAGAAAAAAAATCAG[A/G]GTAATGTTTCCTTCA	8925
rs200079504	snp	C/T	5.39515e-05	0.00519354	missense	HERC1	GRCh38.p7	15:63696261	CTGAACTCAATCTGC[C/T]TCCTGCCAGTGAGAT	8925
rs200084879	snp	A/G	0.00299544	0.0385843	missense	HERC1	GRCh38.p7	15:63678136	TCTCGGCTCTGAACC[A/G]AGCGGCTTTTCTTTA	8925
rs200096405	in-del	-/CT			intron-variant	HERC1	GRCh38.p7	15:63673368	ATATACACCATGTAC[-/CT]CTCTCTCTCTCTATT	8925
rs200118123	snp	C/T	1.65636e-05	0.00287776	synonymous-codon	HERC1	GRCh38.p7	15:63677928	CAGCGTGGCATGGCG[C/T]CCAGTTTGCTTGTGA	8925
rs200126551	snp	A/G	0.00046376	0.0152205	missense	HERC1	GRCh38.p7	15:63680617	CTTGAGTAAAGCTGG[A/G]CAATGTGAGAGTCTG	8925
rs200133130	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63733851	GCAAAACCCTGTCTC[-/A]AAAAAGAAAAATAAA	8925
rs200134702	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63811027	TTAATGTCATTTGGG[-/A]AAAAAAAAAGGCTGG	8925
rs200151191	snp	A/C	0.00167201	0.0288671	synonymous-codon	HERC1	GRCh38.p7	15:63612371	GGAGAACTCTTCCAG[A/C]GTGTGCCAGAACCAC	8925
rs200169757	snp	A/G	0.000680379	0.0184317	synonymous-codon	HERC1	GRCh38.p7	15:63665951	CTCCATTTCAGCAGC[A/G]TCAGCTGATGGTATG	8925
rs200172699	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63822598	CTCAAAAAAAAAAAA[A/T]TTTTTAAATAATAAT	8925
rs200178566	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63699774	AATCTTTACATTAGA[G/T]AGCAAAATGTTAACA	8925
rs200179886	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63781816	AGTTCTTAAAGAAAC[A/C]AAGAAAGCCACTCCA	8925
rs200195706	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63827550	AGTATACTCTCCACA[A/T]AAAAAAGAAGGGAAC	8925
rs200200988	snp	A/G	0.00052126	0.0161356	intron-variant	HERC1	GRCh38.p7	15:63615734	GAGAGAAACCCAAGC[A/G]TTCATGTGTACCTCC	8925
rs200232684	snp	A/C/T	0.000638258	0.0178545	intron-variant	HERC1	GRCh38.p7	15:63628834	GGAATAAATCACAAA[A/C/T]ATACAGACATTCAAT	8925
rs200243610	snp	C/T	0.000383803	0.0138475	missense	HERC1	GRCh38.p7	15:63658704	AGGAGCTCTTTTCTA[C/T]GGAGCCATGGCAACC	8925
rs200245307	snp	A/G	6.81605e-05	0.00583743	missense	HERC1	GRCh38.p7	15:63696168	CCTTGCCTCCTGTGT[A/G]TCCAACAGTGCCTAA	8925
rs200246221	in-del	-/A	0.0414363	0.137845	intron-variant	HERC1	GRCh38.p7	15:63829264	TCTCTACTAAAAATT[-/A]AAAAAAAATCAGCGG	8925
rs200252549	snp	A/T	0.00025149	0.0112108	synonymous-codon	HERC1	GRCh38.p7	15:63694383	GCTAAGCTGGGAAAC[A/T]CCCGTCTTTGGCAAC	8925
rs200254798	in-del	-/TA	0.0433465	0.140692	intron-variant	HERC1	GRCh38.p7	15:63790210	ATAAACGTAAGCTGC[-/TA]TATTATGATCATTAT	8925
rs200263539	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63691368	CTACTTGGGAGGCTG[A/C]GACGGGAGGATCACT	8925
rs200277711	in-del	-/TTA	0.00676609	0.0577691	intron-variant	HERC1	GRCh38.p7	15:63751831	TTATTATTATTATTA[-/TTA]CTATTATTACTACCA	8925
rs200289739	in-del	-/C	0.0287284	0.116357	intron-variant	HERC1	GRCh38.p7	15:63688435	TAGAAGATGGGAATA[-/C]TAAGTCTAGAATTCA	8925
rs200315195	in-del	-/G			intron-variant	HERC1	GRCh38.p7	15:63655527	AGGATTATTATCTAT[-/G]GTTAACTCAAATCAT	8925
rs200318759	snp	C/T	8.28741e-05	0.00643663	missense	HERC1	GRCh38.p7	15:63654231	TGTGCAGCAAGAGTG[C/T]GCACGAGTTGCTGAG	8925
rs200325012	snp	C/T	1.68055e-05	0.0028987	missense	HERC1	GRCh38.p7	15:63624308	CCCCAAGTTCCAGCA[C/T]TATAATGGGATGTGC	8925
rs200327738	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63743263	TCTTTTTTTCTTTTT[C/T]TTTTTTTTTTTTTTT	8925
rs200336717	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63760467	AAAAGACACAAAGGA[A/C]AAACAGAAATCTGAA	8925
rs200343469	in-del	-/AAAC	0.0154538	0.0865337	intron-variant	HERC1	GRCh38.p7	15:63809231	TCTTCATCAAAAAAT[-/AAAC]AAAAATAAAGGCATG	8925
rs200348742	in-del	-/AC			intron-variant	HERC1	GRCh38.p7	15:63718084	GGCAGCTATTATGTG[-/AC]ACACACACACACACA	8925
rs200361336	in-del	-/T	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63730147	AGCTACTTCTATTTG[-/T]TTTTTTCCATTAAAA	8925
rs200362466	snp	C/T	0.000751949	0.0193755	missense	HERC1	GRCh38.p7	15:63690564	TTTGATCATCTTCTA[C/T]ACCAGATTCACAAGC	8925
rs200386807	snp	C/T	0.000350201	0.0132279	synonymous-codon	HERC1	GRCh38.p7	15:63747011	AATGCTGGTAGCTAC[C/T]CCTCCCGCAAGTGCA	8925
rs200416420	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63737016	GAAATTGTCTAATTT[-/A]AAAAAAAAAGTACAT	8925
rs200434599	in-del	-/AC			intron-variant	HERC1	GRCh38.p7	15:63646834	AACAAACAAACAAAA[-/AC]AAAAACAAAACAAAA	8925
rs200436280	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63622325	TGGAAGTGCCTGTTT[C/T]CTTTTTTTTTTTTTT	8925
rs200491054	snp	C/T	3.72093e-05	0.00431315	missense	HERC1	GRCh38.p7	15:63626067	AGCCGGAGCCTGGCC[C/T]GCACCGTGTGAATGC	8925
rs200493456	snp	C/T			synonymous-codon	HERC1	GRCh38.p7	15:63713472	TATTAACAGGGCACA[C/T]CGATGGATCACGGAG	8925
rs200494888	snp	A/G	2.85914e-05	0.00378086	intron-variant	HERC1	GRCh38.p7	15:63696101	ACAGTTAAAATCTGT[A/G]TATACTGCAAGGTGT	8925
rs200527326	in-del	-/CT	0.0197687	0.0974348	intron-variant	HERC1	GRCh38.p7	15:63631921	TTTTCTCATTCTATA[-/CT]CTCTCTCTCTCTGGG	8925
rs200530157	snp	C/T	0.00150475	0.0273881	intron-variant	HERC1	GRCh38.p7	15:63678399	GGTGGAAAACACATG[C/T]TATTAGTAGTTCTTC	8925
rs200536301	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63628953	TCAATAAAACACATT[C/T]TTTTTTTTTTTTTTT	8925
rs200547665	in-del	-/ATG			intron-variant	HERC1	GRCh38.p7	15:63699555	CCCTTTGGGTTTCAT[-/ATG]TAATATAAGGAACAT	8925
rs200551742	snp	A/C	0.00174757	0.0295081	missense	HERC1	GRCh38.p7	15:63630539	GTGTGTTCAGCTCCA[A/C]CTGCCACATCTTCTA	8925
rs200558951	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63697566	TTCAAGTGATTCTCC[C/T]GCCTCAGCCTCCCAA	8925
rs200587499	snp	C/G	0.00299557	0.0385851	missense	HERC1	GRCh38.p7	15:63636086	CACCACTTTCAGTTA[C/G]GGCCATAGAGTGCCC	8925
rs200587720	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63691643	TTACCTTATTAAAGG[-/A]AAAAAAAAGGAGCAG	8925
rs200608524	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63826812	AAAAAAAAAAAAAAA[A/T]AAATATATATATATA	8925
rs200623063	snp	A/T	0.000140092	0.00836818	synonymous-codon	HERC1	GRCh38.p7	15:63672510	CCTGAGAAGACTAAG[A/T]GGCATCACTCCCGGG	8925
rs200625503	snp	A/C/G/T	3.53265e-05	0.00420265	intron-variant	HERC1	GRCh38.p7	15:63656398	GATGGATAAAGAAAA[A/C/G/T]GGATTTCTTAAGGGA	8925
rs200631595	snp	A/C/G	0.000101197	0.00711266	intron-variant	HERC1	GRCh38.p7	15:63716272	AGCATGCCACAGTTT[A/C/G]TATCTAGAAAGTAAG	8925
rs200639203	snp	A/G	0.000117207	0.00765439	synonymous-codon	HERC1	GRCh38.p7	15:63633962	AGTGTGGTTTAATCC[A/G]CAGGCCACCTAAAGA	8925
rs200643599	snp	A/G	3.32917e-05	0.0040798	intron-variant	HERC1	GRCh38.p7	15:63754501	TAAATAATTTTTTAC[A/G]TACCATTGTCTCCTC	8925
rs200680431	snp	A/G	0.000985433	0.0221753	synonymous-codon	HERC1	GRCh38.p7	15:63764123	ACATAATGCTGCCTC[A/G]TAAAGGGAGCACAAG	8925
rs200707469	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63655727	GACTGTATGTTTCAG[C/T]AGTATGAAACTTACC	8925
rs200717910	snp	C/T	4.96841e-05	0.00498393	synonymous-codon	HERC1	GRCh38.p7	15:63674964	TCGTTTGGTGCTCTG[C/T]TTGCCCATGTCTTCA	8925
rs200728024	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63773241	TGAGGTCAGGAGTTC[C/G]AGACCAGCTATGGTC	8925
rs200742146	snp	C/T	0.00441062	0.0467531	missense	HERC1	GRCh38.p7	15:63643504	GGAGTGATGTGTCCC[C/T]GCAGCTGATAAACAC	8925
rs200745033	snp	C/T	0.000424478	0.0145622	missense	HERC1	GRCh38.p7	15:63674573	TGTGGCCATTTTCAG[C/T]CAGAACTTTTGGTAT	8925
rs200748047	snp	A/G	0.000182492	0.00955054	missense	HERC1	GRCh38.p7	15:63623820	CTCGGGAAGGCAGGC[A/G]GAGGTCTGAAGCATT	8925
rs200760220	in-del	-/CTA			intron-variant	HERC1	GRCh38.p7	15:63688434	GTAGAAGATGGGAAT[-/CTA]ATAAGTCTAGAATTC	8925
rs200768642	snp	C/G/T	3.31614e-05	0.00407181	missense	HERC1	GRCh38.p7	15:63753007	CTCCCAGCACAAACT[C/G/T]TGCGAATGAACATTC	8925
rs200797365	in-del	-/CATA			intron-variant	HERC1	GRCh38.p7	15:63660365	ATACATACATACATA[-/CATA]AAATGCAGATGGACT	8925
rs200853874	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63728935	TAAAGAAAGAGCAGG[-/T]TTTTAAAAAAAAAAA	8925
rs200856543	in-del	-/GAA			intron-variant	HERC1	GRCh38.p7	15:63809009	CCTAAAATAAAAAAT[-/GAA]GAAATAGCAAAAATA	8925
rs200890961	snp	A/G	0.000165637	0.00909896	synonymous-codon	HERC1	GRCh38.p7	15:63645097	GCCACTCTGACAGCC[A/G]CTTAAAAAAATTGAT	8925
rs200898269	snp	C/T	0.00014906	0.00863178	missense	HERC1	GRCh38.p7	15:63686444	GTTAAAATCTGTCCA[C/T]TCTCCACTAGGCAAC	8925
rs200920211	snp	A/C	0.000166445	0.00912111	intron-variant	HERC1	GRCh38.p7	15:63723160	AACTACAAATTTACT[A/C]CCTTTATCTTCTTTA	8925
rs200928970	snp	A/C	0.00299544	0.0385843	missense	HERC1	GRCh38.p7	15:63674737	TGATTTTTTCTTTTC[A/C]CTTCTGTTATTTGAT	8925
rs200934611	in-del	-/CAGA			intron-variant	HERC1	GRCh38.p7	15:63760470	CAAAGGAAAAACAGA[-/CAGA]AATCTGAATTACAAA	8925
rs200964205	snp	C/T	0.000398063	0.0141022	missense	HERC1	GRCh38.p7	15:63678127	TCATTTTCCTCTCGG[C/T]TCTGAACCGAGCGGC	8925
rs200964231	snp	A/G	3.71092e-05	0.00430735	missense	HERC1	GRCh38.p7	15:63643025	TCTGAATAGCTCCAG[A/G]GCCTATCACAACAGT	8925
rs200979460	in-del	-/GG	0.0422008	0.138995	intron-variant	HERC1	GRCh38.p7	15:63833792	ACACACACACACACA[-/GG]ACCAGGAGGACGGTA	8925
rs200983374	snp	C/T	0.000217565	0.0104276	missense	HERC1	GRCh38.p7	15:63649736	TTACCATCCTTTCGA[C/T]AGCAATGCTCCAATT	8925
rs200986714	snp	A/G	0.000344931	0.0131281	intron-variant	HERC1	GRCh38.p7	15:63775657	CATTAGTCCTGCAAA[A/G]GGAGAAGAGAAAACA	8925
rs200988839	snp	A/G	1.65583e-05	0.00287731	missense	HERC1	GRCh38.p7	15:63661874	ACCAGCCATCCACAT[A/G]GGAACCATTGCTGCG	8925
rs200989567	in-del	-/T	0.0107246	0.0724382	intron-variant	HERC1	GRCh38.p7	15:63705544	TTTCCCTCATTTCTG[-/T]TTTTTTTTCTATGGA	8925
rs201044362	snp	A/G	0.000206037	0.0101477	synonymous-codon	HERC1	GRCh38.p7	15:63678351	GCCACGCATCTGCAT[A/G]TCACAAATTTTCACC	8925
rs201049016	in-del	-/AA			intron-variant	HERC1	GRCh38.p7	15:63829478	CATATATGTTTATAT[-/AA]ATATATATATATATA	8925
rs201060589	snp	C/T	3.32519e-05	0.00407736	missense	HERC1	GRCh38.p7	15:63775542	CCTCTCTTGTAGCAA[C/T]AGATTCACTGTCCTC	8925
rs201087034	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63673627	GATACAAGATAAAAC[-/A]AGAGCTTTTCTTTTT	8925
rs201114053	snp	A/T	0.000536465	0.016369	intron-variant	HERC1	GRCh38.p7	15:63723366	TTTATCTAAAAAAAA[A/T]ACTCACGTTACCAAT	8925
rs201126069	snp	A/G	0.000198814	0.00996832	intron-variant	HERC1	GRCh38.p7	15:63694737	CTCGGGCTAAAATGT[A/G]ACCTGCACTGTACAT	8925
rs201195137	in-del	-/AC			intron-variant	HERC1	GRCh38.p7	15:63737494	CAGATATATATATAT[-/AC]ATATATATATCTTTT	8925
rs201209419	snp	G/T	0.0012462	0.0249309	intron-variant	HERC1	GRCh38.p7	15:63652586	ATTTTCTATTCAAAT[G/T]ATTTTATTATTTGAA	8925
rs201213378	in-del	-/TTA	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63739918	TAGCATATTTTATTT[-/TTA]TTTTTTTTTTCAGAC	8925
rs201217308	snp	A/G/T	9.0112e-05	0.00671177	intron-variant	HERC1	GRCh38.p7	15:63612594	ATTCAATGAGTGTGC[A/G/T]TGAACCTGGCACCCA	8925
rs201226535	snp	G/T	8.45587e-05	0.00650171	missense	HERC1	GRCh38.p7	15:63674666	GGTAAAGATAGGACA[G/T]CTGGACTGCTCTGAT	8925
rs201228918	snp	A/G	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63618504	CTTTTTTGGTTCCAT[A/G]TGAACTTTAAAGTAG	8925
rs201249478	snp	A/T	0.000106521	0.0072972	intron-variant	HERC1	GRCh38.p7	15:63694167	TAGGTCCTATGTGAA[A/T]TAAAAGAAAAAAATA	8925
rs201261137	in-del	-/A	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63728144	TTTTATAATTTACTC[-/A]AAGAAATATTTATTT	8925
rs201263833	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63721038	TCACCTTATATCTAG[-/T]TTTTTTTTTAGTTCT	8925
rs201277582	in-del	-/AAAG	0.0256215	0.110247	intron-variant	HERC1	GRCh38.p7	15:63674183	TAGAAAAATAATAAA[-/AAAG]AACTGTTTTCAAGAA	8925
rs201286464	snp	C/G	3.31175e-05	0.00406911	missense	HERC1	GRCh38.p7	15:63612479	CCCACACACCATCTG[C/G]TCCAGTTGTTTTGCT	8925
rs201312041	snp	C/T	0.000269197	0.0115985	missense	HERC1	GRCh38.p7	15:63656276	CTCTCCCTGCTGCTG[C/T]CAAGCACATTAATCG	8925
rs201313531	in-del	-/ACAG			intron-variant	HERC1	GRCh38.p7	15:63760469	AGACACAAAGGAAAA[-/ACAG]ACAGAAATCTGAATT	8925
rs201315565	in-del	-/AC			intron-variant	HERC1	GRCh38.p7	15:63701766	TTTGACATCAAAAAG[-/AC]TTAAAACACAAAAAT	8925
rs201335263	snp	C/T	0.000310008	0.0124462	missense	HERC1	GRCh38.p7	15:63712876	GGACTAGCCGGCTCT[C/T]TGCAGTAAGACTTTC	8925
rs201336383	in-del	-/TA	0.16911	0.236552	intron-variant	HERC1	GRCh38.p7	15:63766251	TAATACTAATTTATT[-/TA]TGTTATATTATATAT	8925
rs201337501	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63786295	AAAAAAAAAAAAAAA[C/T]AAGAAGAAGAAGAAT	8925
rs201341185	snp	C/T	7.96844e-05	0.00631157	intron-variant	HERC1	GRCh38.p7	15:63652588	TTTCTATTCAAATGA[C/T]TTTATTATTTGAAAA	8925
rs201351066	snp	A/G	8.28329e-05	0.00643503	synonymous-codon	HERC1	GRCh38.p7	15:63733005	GCAGCTCTGAGTGCC[A/G]TAAGGTTGATCTGAC	8925
rs201362777	snp	A/C/G	9.95312e-05	0.00705385	missense, synonymous-codon	HERC1	GRCh38.p7	15:63753015	ACAAACTTTGCGAAT[A/C/G]AACATTCCTTGTAAA	8925
rs201366252	snp	A/G	3.53738e-05	0.00420543	intron-variant, synonymous-codon	HERC1	GRCh38.p7	15:63654365	ATGGGCATACAATTG[A/G]GCAATTAAACCTGCT	8925
rs201368473	in-del	-/C	0.0142736	0.0832652	intron-variant	HERC1	GRCh38.p7	15:63686266	TTACATATCACGATT[-/C]TTTTTTCAGTCTTTC	8925
rs201376326	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63747925	TGCACGATCAAAAAC[A/G]AAAATTAAAACATAT	8925
rs201387092	snp	A/G	0.000682347	0.0184583	missense	HERC1	GRCh38.p7	15:63756711	CTAACAGAGCCATCC[A/G]TAGAAATGACAAAAG	8925
rs201399853	in-del	-/GA			intron-variant	HERC1	GRCh38.p7	15:63755130	ACTAACAAAATAAAT[-/GA]CAGTCTTTGGCCTAG	8925
rs201438973	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63760469	AAGACACAAAGGAAA[A/G]ACAGAAATCTGAATT	8925
rs201443157	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63829543	TGTGCACATATATGT[A/G]TGTGTGTGTGTGTGT	8925
rs201445321	in-del	-/CCAG	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63619320	TTTTCGTATGTTGAA[-/CCAG]CCTTGCATCCCAGGG	8925
rs201465812	in-del	-/ACACACACACACAC			intron-variant	HERC1	GRCh38.p7	15:63718084	GGCAGCTATTATGTG[-/ACACACACACACAC]ACACACACACACACA	8925
rs201468213	snp	A/C/T	0.000383861	0.0138489	intron-variant	HERC1	GRCh38.p7	15:63669498	CCCACACATCTGGAA[A/C/T]GCCAACTTTGGATAT	8925
rs201470593	snp	A/G	6.67768e-05	0.00577789	synonymous-codon	HERC1	GRCh38.p7	15:63713562	TTGCTGAGACTGAGG[A/G]GGTGGATCATCAGCT	8925
rs201477937	snp	G/T	3.31928e-05	0.00407373	missense	HERC1	GRCh38.p7	15:63675033	AGCCGTCAGGCCTCG[G/T]AATCGCGCCACATCA	8925
rs201499820	in-del	-/T	0.26818	0.249338	intron-variant	HERC1	GRCh38.p7	15:63675904	TATACTGTATACATC[-/T]TTTTTTTTTTTTTTT	8925
rs201503479	snp	A/G	3.36027e-05	0.00409881	intron-variant	HERC1	GRCh38.p7	15:63628833	GGGAATAAATCACAA[A/G]TATACAGACATTCAA	8925
rs201523092	snp	C/T	6.90632e-05	0.00587595	missense	HERC1	GRCh38.p7	15:63674642	CACTAAGTGACTTCA[C/T]AGCACCGAGGTAAAG	8925
rs201530332	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63725153	TTCTTAGGGCTCCAA[A/G]TCATAGCCCCAGATT	8925
rs201552316	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63736814	GTTTCACCATGTTGG[C/G]CAGGCTGGTCTCGAA	8925
rs201563473	snp	A/G	0.0039921	0.0444985	intron-variant	HERC1	GRCh38.p7	15:63733205	CTAGAAAAGAACACA[A/G]AAGGATCCCAGAAAA	8925
rs201569757	snp	C/T	0.00399197	0.0444977	intron-variant	HERC1	GRCh38.p7	15:63643596	AATAAAGATAAATTA[C/T]ATAAGTTCAAGATTT	8925
rs201594188	snp	A/C	0.0287284	0.116357	intron-variant	HERC1	GRCh38.p7	15:63688433	TAGTAGAAGATGGGA[A/C]TATAAGTCTAGAATT	8925
rs201617716	in-del	-/GGT			intron-variant	HERC1	GRCh38.p7	15:63731994	ATAAAGGGTCTGAAG[-/GGT]GGTGGTGGTGGTGGT	8925
rs201624620	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63676649	TAATCCCAGCTACTC[A/G]GAAGACTGAGGTGGG	8925
rs201631505	snp	G/T	0.000364764	0.0135	missense	HERC1	GRCh38.p7	15:63774797	ATGGTGTGTACAACT[G/T]CCGAAGCCCCCAAAG	8925
rs201668167	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63709165	TAATATATATATATA[-/T]TTTTTTATTTTTTTG	8925
rs201668548	in-del	-/A	0.00712654	0.0592662	intron-variant	HERC1	GRCh38.p7	15:63680491	AACCGAGTTGACTAT[-/A]AATAGAAACAAGAAA	8925
rs201690555	snp	A/G/T	0.000733925	0.0191429	synonymous-codon	HERC1	GRCh38.p7	15:63686527	TTCTTCTTCCAACTC[A/G/T]CCCTGCTTCTACCAG	8925
rs201695207	snp	C/G	1.772e-05	0.00297652	intron-variant	HERC1	GRCh38.p7	15:63729388	GAAGAAAAAAAGTTC[C/G]TAAATTACTACTTTG	8925
rs201703621	in-del	-/C	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63683768	ATCCTCCAGCCTCTG[-/C]CTTCCAAGTACTGGG	8925
rs201705794	snp	A/T	0.00299544	0.0385843	missense	HERC1	GRCh38.p7	15:63648070	AAAGATGCATTTACC[A/T]TATGTGCATCAATTA	8925
rs201715626	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63780093	AGGTTCCAATCTGAA[C/T]TGCATTAGATTTATG	8925
rs201751682	snp	C/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63822733	AAAACAAGGAAACCA[C/G]ATAAGAGACTATTAT	8925
rs201769820	snp	A/G	1.65745e-05	0.00287871	missense	HERC1	GRCh38.p7	15:63718838	TCAGAAGAGCTGCAA[A/G]AACAAATCTAGACAC	8925
rs201774840	snp	A/G	9.94678e-05	0.00705153	intron-variant	HERC1	GRCh38.p7	15:63694725	TAGTACCATAACCTC[A/G]GGCTAAAATGTAACC	8925
rs201779072	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63684058	AGTCTGAAAAACATC[G/T]TGGATGCTGGCTGGA	8925
rs201817580	in-del	-/A	0.179425	0.239831	intron-variant	HERC1	GRCh38.p7	15:63693186	TGTCTCAACAACAAC[-/A]AAAAAAAACCCAGAA	8925
rs201819784	snp	C/G	9.94299e-05	0.00705018	missense	HERC1	GRCh38.p7	15:63623787	CAGCCCCTTCTCCAA[C/G]CAGCTTAACCTTCCA	8925
rs201836684	snp	C/T	3.31301e-05	0.00406989	missense	HERC1	GRCh38.p7	15:63674911	TTCTGCTCAACATCC[C/T]CTTTCTCCTCGGATT	8925
rs201849193	snp	A/C/T	4.97536e-05	0.00498746	missense	HERC1	GRCh38.p7	15:63698823	AACCTGGGGCATTCC[A/C/T]CACATCTCCACTCAC	8925
rs201857266	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63611547	GAGGTTATCGTTGCT[C/T]CCCACATCTTTGGGT	8925
rs201867653	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63723075	ATATCTTTTTCTATT[-/A]AAAAAAAAGGGTGAT	8925
rs201870026	snp	A/G	0.000579456	0.0170115	synonymous-codon	HERC1	GRCh38.p7	15:63612407	CAGCTGATGCTGCTC[A/G]TCCACCTCACGGTAC	8925
rs201872646	in-del	-/TT	0.0287284	0.116357	intron-variant	HERC1	GRCh38.p7	15:63688432	TAGTAGAAGATGGGA[-/TT]ATATAAGTCTAGAAT	8925
rs201872684	snp	C/T	1.65919e-05	0.00288022	missense	HERC1	GRCh38.p7	15:63624272	GGGGCTAACAAAGGC[C/T]GAAGTTGTCCCTGTA	8925
rs201949584	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63828050	TAGATAGTTGTGATG[A/G]TTGCACCATCTTGTG	8925
rs201958813	in-del	-/AG	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63655260	TTGGGAGGCTGAGGC[-/AG]GAGAATCACTTGAGC	8925
rs201961752	snp	C/G/T	0.000283799	0.0119094	missense	HERC1	GRCh38.p7	15:63651375	CTTTCCTCAGCATCC[C/G/T]CTTCCCTAGAATATA	8925
rs201974971	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63631281	GCAAAGTCTGCTAGG[C/T]CCATTTGGCTTGCCC	8925
rs201996483	snp	A/C/T	1.80866e-05	0.00300715	missense	HERC1	GRCh38.p7	15:63643432	ATGTTCATGAGCCCA[A/C/T]CTAGTCCACCAGACA	8925
rs202016769	in-del	-/T	0.0252325	0.109451	intron-variant	HERC1	GRCh38.p7	15:63718491	AATAACCAAGGCACA[-/T]TTTTTTTCTCACATA	8925
rs202024869	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63786920	ACTCAATAAATTATT[-/A]TTTTTTTTTTTTTTA	8925
rs202030170	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63743264	CTTTTTTTCTTTTTC[-/T]TTTTTTTTTTTTTTT	8925
rs202036504	in-del	-/AC			intron-variant	HERC1	GRCh38.p7	15:63717734	AAATTAGCAGGGCGT[-/AC]GGTGGTGCATGCCTG	8925
rs202041791	snp	A/C/T	3.76712e-05	0.00433983	missense	HERC1	GRCh38.p7	15:63723280	ACAGCAATTTCAGGC[A/C/T]GCAATTTATAATCAA	8925
rs202086716	snp	C/G	0.0039921	0.0444985	missense	HERC1	GRCh38.p7	15:63654310	CTGCCAGGGCATTAG[C/G]CAACTCCAGAGGGCC	8925
rs202087825	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63705318	GCATCCACGCCTAGC[-/T]TTTTTTTTTCTTTTT	8925
rs202095127	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63689129	TGGCAGAGAATATAC[A/G]GAGATCCGGGAGAAA	8925
rs202100265	snp	C/G	0.00299557	0.0385851	missense	HERC1	GRCh38.p7	15:63725370	TGTCCTGTTCCTCTG[C/G]AGACACAGGGGAGCC	8925
rs202113858	snp	C/T	0.000169986	0.00921759	missense	HERC1	GRCh38.p7	15:63690547	AATAAAAACCTGGGC[C/T]ATTTGATCATCTTCT	8925
rs202115539	snp	C/G	1.65707e-05	0.00287838	missense	HERC1	GRCh38.p7	15:63678009	CAGCACGGGCCACAC[C/G]TCTATGCAAAGAGTC	8925
rs202120102	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63739919	AGCATATTTTATTTT[-/A]TTTTTTTTTCAGACA	8925
rs202125401	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63617949	TTTTCTCCCATTCTG[-/A]TGGGTCGCCTGTTCA	8925
rs202128593	snp	A/C	0.000325947	0.0127619	missense	HERC1	GRCh38.p7	15:63665956	TTTCAGCAGCATCAG[A/C]TGATGGTATGTCTCC	8925
rs202130230	snp	C/T	0.000161207	0.00897649	missense	HERC1	GRCh38.p7	15:63678340	TCTCGGGGTGTGCCA[C/T]GCATCTGCATATCAC	8925
rs202145791	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63740103	TTTAGTAGAGACAGG[A/G]TTTCACCATTTGGCC	8925
rs202148901	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63619441	ATGTTCATCAAGGAT[A/G]TTGGTCTAAAATTCT	8925
rs202150256	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63720484	AAAAATTTTTAGCCT[A/C]AAATTAATTTTGGTT	8925
rs202170792	snp	G/T	0.000168799	0.00918537	intron-variant	HERC1	GRCh38.p7	15:63659713	ATGCTATAAAATCAA[G/T]GCAAATCAGGATTTC	8925
rs202182659	snp	C/T	0.000149196	0.00863571	missense	HERC1	GRCh38.p7	15:63749437	GCTGAATAGCTATGC[C/T]ATCTAAGCCACTCAC	8925
rs202195874	snp	C/T	0.00125318	0.0250004	missense	HERC1	GRCh38.p7	15:63655772	CTGACTTATCATAGT[C/T]AGGTCTTAGTTTGGC	8925
rs202204675	in-del	-/A	0.030278	0.119257	intron-variant	HERC1	GRCh38.p7	15:63799205	ACTTAAGGCTTTAAC[-/A]AAAAGTAGCTATTGG	8925
rs202206215	snp	A/C/T	0.00012298	0.00784068	intron-variant	HERC1	GRCh38.p7	15:63666154	CTCCCCTAGCACCTA[A/C/T]ACAGGGGAAAAACAG	8925
rs202244454	snp	A/C	1.65751e-05	0.00287876	stop-gained	HERC1	GRCh38.p7	15:63774819	CCCCCAAAGCCATTT[A/C]TATCCATTCAAGAAG	8925
rs207475555	snp	A/G			synonymous-codon	HERC1	GRCh38.p7	15:63640221	AGATTCTGGAAACTG[A/G]GCTCCATTGGTCAGG	8925
rs267604281	snp	A/G			synonymous-codon	HERC1	GRCh38.p7	15:63623863	TTGTCTCGCTATTTG[A/G]ACAAAAATAGGCTTA	8925
rs267604282	snp	A/C			stop-gained	HERC1	GRCh38.p7	15:63674945	GTCGGTGTTTCTTTT[A/C]ATGTCGTTTGGTGCT	8925
rs367546940	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63788898	AAAAAAAAAAATTTA[A/G]CAATGAAAATGAGAA	8925
rs367550280	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63808239	TGTAATGATTCTGAA[A/T]AACGGCTGCTATCAA	8925
rs367550920	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63762231	CTGAAGAGACTAATA[A/G]CCAAAAATGAAACAA	8925
rs367559501	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63828144	ATGGCAATAAGTAAC[A/T]GTATCAGAAGAAAAG	8925
rs367570446	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63819272	TTCAGGGGCTCATTC[C/T]TAAGGCAGCTCCCTC	8925
rs367585281	snp	G/T	1.65891e-05	0.00287998	missense	HERC1	GRCh38.p7	15:63616520	ATCCACCTCCTCCAG[G/T]TCCTCTAGGGTGAGT	8925
rs367588555	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63679348	ATTAAAAATATGTAT[G/T]TTTAAAAACATAGAA	8925
rs367591428	snp	A/G	3.347e-05	0.00409071	intron-variant	HERC1	GRCh38.p7	15:63638397	TCTTTTCTATTTTTT[A/G]TCCTGTTAGTTACCT	8925
rs367611317	snp	G/T	9.51629e-05	0.00689727	missense	HERC1	GRCh38.p7	15:63645597	CAGCATCCCGAAATA[G/T]AGCCCCAGAGTTTCA	8925
rs367615804	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63770278	ACCTCAGGGGTACTT[C/G]CTCCGTAAGACATTT	8925
rs367621148	snp	C/G	0.000159987	0.00894248	missense	HERC1	GRCh38.p7	15:63674820	ATTTTCTGATTTGGA[C/G]CTTGTGGTACTCTGA	8925
rs367624878	in-del	-/A/AA			intron-variant	HERC1	GRCh38.p7	15:63780012	GGGAGACTCCATCTC[-/A/AA]AAAAAAAAAAAAAAA	8925
rs367626289	snp	C/G/T	0.00485185	0.0490184	intron-variant	HERC1	GRCh38.p7	15:63659966	AATAAATGTATAGTA[C/G/T]GTGAATTTAAATATT	8925
rs367626413	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63710037	CAAGAGGTATGCTTG[G/T]GGTCTGGCAGATGAA	8925
rs367635603	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63693274	TTTGAGACAGGCTCT[C/T]GCTCTGTCATCCAGG	8925
rs367646650	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63673254	ATCCTACAAATAAAC[A/C]TAACTAAAATATGAG	8925
rs367651555	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63799536	AGAAAAAGAAAAATA[C/T]TGATCCTTTCTGCCA	8925
rs367657849	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63764366	TGCAAGGAAGTTTTA[A/T]TAAACGAGCTGGCTA	8925
rs367668344	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63809007	TCCCTAAAATAAAAA[A/C]TGAAGAAATAGCAAA	8925
rs367708752	snp	A/G	6.628e-05	0.00575635	synonymous-codon	HERC1	GRCh38.p7	15:63640191	TGGAACAGGTTCTAG[A/G]TCTGGAACGGTAAAA	8925
rs367715460	snp	A/G	0.000167986	0.00916323	missense	HERC1	GRCh38.p7	15:63663163	ATATTCCTTCTCTCC[A/G]ACTTTGATTCCTGTG	8925
rs367720452	snp	C/G	4.35152e-05	0.0046643	missense	HERC1	GRCh38.p7	15:63615856	GGGATACTATTTCCA[C/G]CAGGGATTATAGGAA	8925
rs367724056	snp	C/T	0.000163987	0.00905353	intron-variant	HERC1	GRCh38.p7	15:63658497	GACTTCCAGCTAATG[C/T]ACACTAGAAGTTAAC	8925
rs367739179	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63831875	GCTTTCTCTTCCATG[A/C]AACATCAGGGTGCCT	8925
rs367740632	snp	A/G	1.65627e-05	0.00287769	missense	HERC1	GRCh38.p7	15:63725474	GACTGAGCTGGCTGA[A/G]GTAATGGCAGACCAG	8925
rs367746487	snp	C/T	0.000159987	0.00894249	missense	HERC1	GRCh38.p7	15:63678055	GAGAGGTCAGCGAGG[C/T]CATGCCTAGTATGTT	8925
rs367750871	snp	C/T	1.79403e-05	0.00299497	synonymous-codon	HERC1	GRCh38.p7	15:63756665	GGAGTCTCCAAGGCC[C/T]AGTCTCCCATAGCTG	8925
rs367757111	snp	C/T	8.35275e-05	0.00646195	intron-variant	HERC1	GRCh38.p7	15:63716295	AAAGTAAGAAGGGTA[C/T]ACTCACTGCCAGCTG	8925
rs367757143	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63819344	CCTGCCTGTCTCACA[C/G]AGGTGTTATTCACAT	8925
rs367784998	snp	A/G	1.65817e-05	0.00287933	synonymous-codon	HERC1	GRCh38.p7	15:63775186	CCGGGGGCGTTCACT[A/G]ACAGAATGGACATCT	8925
rs367796952	snp	C/G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63643944	CACATGCTGACTCTA[C/G/T]ATAAATAGATTCCTC	8925
rs367856368	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63788297	TGCATTTCAAAAAAA[A/C]CAATTTAACAGTTAT	8925
rs367861526	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63809605	TTGAGTTGAGAAATA[C/T]GGGCCTAAAATAAAA	8925
rs367865079	snp	A/C	3.31868e-05	0.00407336	missense	HERC1	GRCh38.p7	15:63754522	TTGTCTCCTCCTCCA[A/C]AAGACCATACAGTTC	8925
rs367875167	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63744140	TGTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT	8925
rs367884370	snp	A/C/G	0.00012822	0.00800604	intron-variant	HERC1	GRCh38.p7	15:63623934	ATACAACTCTTACCA[A/C/G]TTTCCCCAAAATCAC	8925
rs367911641	snp	A/C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63817701	GTGTGGGTGACACAG[A/C/T]GAGACTCTGTCTCAA	8925
rs367931850	snp	C/T	2.68532e-05	0.00366413	synonymous-codon	HERC1	GRCh38.p7	15:63641572	ACCCTGCTGTTTCAA[C/T]GCTGTCCTACAGGTT	8925
rs367944555	snp	C/G	0.000248453	0.0111429	synonymous-codon	HERC1	GRCh38.p7	15:63654191	ATCAGCAAGTGTCTG[C/G]AGAGTAGTTTGGTTG	8925
rs367947679	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63761976	TCTGTCTACCATGAA[C/T]ATAAAAACCTAGAAA	8925
rs367954573	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63651572	GAAAAATGAATTATA[A/T]AAGAGTGATATTAGA	8925
rs367959308	snp	C/T	1.88695e-05	0.00307155	missense	HERC1	GRCh38.p7	15:63666142	GGGCATCAGCCTCTC[C/T]CCTAGCACCTATACA	8925
rs367959756	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63691584	CAGTTGAAAATAAAT[C/G]AATATCTGATTTTTC	8925
rs367961570	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63691055	GTTTTAAACAGGTCT[C/G]TTAATCTCCAAAGCT	8925
rs367964987	snp	A/G	4.96824e-05	0.00498385	missense	HERC1	GRCh38.p7	15:63680722	CATGTACTGGCCAGC[A/G]AGAAACTCCAACACA	8925
rs367971124	snp	C/T	0.000292976	0.0120997	synonymous-codon	HERC1	GRCh38.p7	15:63648096	AATTAGAACAATGCC[C/T]CCTTTCTCAAGTGGT	8925
rs367976958	in-del	-/AT			intron-variant	HERC1	GRCh38.p7	15:63681798	AGAAACATCACACAC[-/AT]GTTATTTTTCTTGCT	8925
rs367981307	snp	C/T	5.01626e-05	0.00500787	synonymous-codon	HERC1	GRCh38.p7	15:63698980	ACTCAGGGATTCCAA[C/T]TGACTGTGCATAGGA	8925
rs367997811	snp	C/T	6.62932e-05	0.00575693	missense	HERC1	GRCh38.p7	15:63674879	TTCGCATATCTAAAG[C/T]GGATTCACTCTCAGG	8925
rs368001971	snp	C/G/T	6.55434e-05	0.00572435	intron-variant	HERC1	GRCh38.p7	15:63774668	AAACTATTATGAACT[C/G/T]TAAAGTTGAGACTTA	8925
rs368009541	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63750505	TGAATGATTTTTTTT[A/C]TTTATCTTCAATAGA	8925
rs368019787	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63618821	TGGTGTATAAGAATG[C/T]TTGTGATTTTTGCAC	8925
rs368022123	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63615593	CCAGCCTAGGCGACA[C/G]AGTGAGGTGCTGTCT	8925
rs368022458	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63670767	ACCATATTAGAATGT[C/T]GTATCAGGCAAGCAT	8925
rs368023184	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63633840	CCTAGACTCAAGGCA[A/G]TACTGACCTGAGGTG	8925
rs368023423	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63670687	CTGAAAAGGTTACAA[C/G]GAGTCACAGTGCTAC	8925
rs368023935	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63655513	TAAAGAAACCTACCA[C/G]GATTATTATCTATGG	8925
rs368027433	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63700173	CGTTGACTTTTAAAA[A/G]AGAGTATCATTTTAT	8925
rs368029299	snp	A/G	0.000104118	0.00721444	intron-variant	HERC1	GRCh38.p7	15:63718744	TTTCTGACATCATGA[A/G]AGCAAATATTTGTCT	8925
rs368034502	snp	C/T	0.000167986	0.00916323	intron-variant	HERC1	GRCh38.p7	15:63638401	TTCTATTTTTTATCC[C/T]GTTAGTTACCTGTTG	8925
rs368034821	snp	C/T	0.000182371	0.00954738	intron-variant	HERC1	GRCh38.p7	15:63661047	CAAACATGAAGAACA[C/T]TGCATTTTTATATAA	8925
rs368043430	snp	A/T	6.64673e-05	0.00576448	intron-variant	HERC1	GRCh38.p7	15:63729450	ATCCAAATATCTGAG[A/T]TTCAAGGTCCCTGAT	8925
rs368044703	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63713123	TTTTTCACTGCTGTT[C/G]TTTATATATACGAAA	8925
rs368047551	snp	A/G	4.98965e-05	0.00499457	missense	HERC1	GRCh38.p7	15:63694489	GCCAAAGAAACATCT[A/G]CTGGTTGATAATGAA	8925
rs368054222	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63647381	AGTGGTGAAAAGGGA[A/G]CTCTTAAACACTGTT	8925
rs368054962	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63780012	AGGGAGACTCCATCT[A/C]AAAAAAAAAAAAAAA	8925
rs368062090	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63610688	GCAGCAGCCTGCAGC[C/G]TCAGGAGGCAGCACA	8925
rs368079699	snp	A/T	8.41036e-05	0.00648419	intron-variant	HERC1	GRCh38.p7	15:63664420	GTGCCTTTACATTGC[A/T]TTCAAAATAAGATCT	8925
rs368079926	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63639107	TGTGGGCAAATTACT[A/T]CATCTTTCTGGGCTT	8925
rs368089986	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63813755	GAGATCAAATGCCTA[C/T]CAATGTCCTCTTTCA	8925
rs368093789	snp	C/T	9.95074e-05	0.00705293	missense	HERC1	GRCh38.p7	15:63678116	CCTCTCTCATTTCAT[C/T]TTCCTCTCGGCTCTG	8925
rs368105722	in-del	-/T	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63763579	TTTAAAAGACTTTCC[-/T]TTTTTTTTTTTTTAA	8925
rs368113274	snp	C/T	1.65715e-05	0.00287845	synonymous-codon	HERC1	GRCh38.p7	15:63725500	ACCAGCAGGATCAAT[C/T]AGTTCTGGCCCTCCT	8925
rs368156164	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63766042	GCGACCTGTCTCAGA[C/T]AGTTTTTGGTTTACA	8925
rs368177203	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63783755	TAAAAGCAGTAGACC[A/G]TGACTCCCCAAAGAA	8925
rs368205897	snp	A/C			upstream-variant-2KB	HERC1	GRCh38.p7	15:63834045	GCCCCGCCCAACAGG[A/C]CCAGCGCGGGAGGTG	8925
rs368208689	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63833391	CACTCCCCGGACCCT[A/G]AGAGGGAGTCGGCCG	8925
rs368211214	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63794174	ATAACCATAAAAATG[A/G]GCAACCAGCAGCCCT	8925
rs368216902	snp	C/T	0.000165986	0.00910855	missense	HERC1	GRCh38.p7	15:63640241	CATTGGTCAGGGCTT[C/T]GGCAGCTTTTATAGT	8925
rs368217073	snp	G/T	3.57878e-05	0.00422997	missense	HERC1	GRCh38.p7	15:63672526	GGCATCACTCCCGGG[G/T]ACTCGGATGCAGGCA	8925
rs368223552	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63822599	TCAAAAAAAAAAAAA[-/T]TTTTAAATAATAATT	8925
rs368224518	snp	C/T	1.67506e-05	0.00289396	missense	HERC1	GRCh38.p7	15:63690554	ACCTGGGCCATTTGA[C/T]CATCTTCTACACCAG	8925
rs368224538	snp	G/T	3.31472e-05	0.00407093	synonymous-codon	HERC1	GRCh38.p7	15:63624214	TTTGCCTTGAACCAT[G/T]GTTTTTCCTATGGAG	8925
rs368228102	snp	C/T	0.000100408	0.00708478	missense	HERC1	GRCh38.p7	15:63651277	GCCAGATATTCACCA[C/T]CTTTTCCAAAGCGCC	8925
rs368233302	snp	A/G	1.71855e-05	0.00293129	synonymous-codon	HERC1	GRCh38.p7	15:63634868	AGTGACCACTGCTGA[A/G]TGCTTGAAGCCACAA	8925
rs368242696	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63695091	CCCATGCTGGGGTGC[A/G]GTGGTGCAATCCTGG	8925
rs368247878	snp	C/G	6.72947e-05	0.00580025	missense	HERC1	GRCh38.p7	15:63656321	TATCTGTTAGCCCCA[C/G]AGACTCAAGACCAGC	8925
rs368269544	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63648346	CATTTAGACAAAATG[G/T]AGGCGTACAGTGGGG	8925
rs368294960	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63741341	CCATCTTTTTTTTTT[-/T]GAGACAGAGTTTCAT	8925
rs368295742	snp	A/G/T	0.00015999	0.0089428	intron-variant	HERC1	GRCh38.p7	15:63666192	CTGACTTTGGGCAAA[A/G/T]AATTAGGTCTTTATG	8925
rs368296809	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63772193	ATGCATACAAGCCTA[C/G]ACAATGAGGCTAAAT	8925
rs368315540	snp	A/G	3.3173e-05	0.00407252	intron-variant	HERC1	GRCh38.p7	15:63729491	AAAAGACAAATAATC[A/G]CATACCTCACTAATG	8925
rs368323380	snp	C/G	5.06675e-05	0.00503301	missense	HERC1	GRCh38.p7	15:63774722	ATCTGCATTAATATG[C/G]TCATAAAGCAGTCAA	8925
rs368330368	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63702105	ACCATAAAATATGTA[A/G]GCAAGCTAAAAGGGG	8925
rs368363192	in-del	-/TA			intron-variant	HERC1	GRCh38.p7	15:63701906	GAAAAGGGCATTAAA[-/TA]AGCTTCTACATAACA	8925
rs368376049	snp	A/C	0.000152507	0.00873101	intron-variant	HERC1	GRCh38.p7	15:63630458	CAGCAAGCAATATAA[A/C]TATTTACCTGCCCTT	8925
rs368385929	snp	A/C	4.97179e-05	0.00498562	synonymous-codon	HERC1	GRCh38.p7	15:63654224	ACGGTCGTGTGCAGC[A/C]AGAGTGCGCACGAGT	8925
rs368397438	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63818375	AAACCCTTTCCTGCC[C/T]GCCTACTCTGAAATA	8925
rs368411323	snp	A/C	8.30296e-05	0.00644266	intron-variant	HERC1	GRCh38.p7	15:63725517	GTTCTGGCCCTCCTA[A/C]AGACAAAATCATTAG	8925
rs368412725	snp	A/C	1.65674e-05	0.00287809	missense	HERC1	GRCh38.p7	15:63758233	ATTTTCTCCTGTGTA[A/C]CTTCTACCAACTGAT	8925
rs368432842	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63673478	ATAAACTCCATGAAG[A/G]CAAGGGACTTTGTTT	8925
rs368451078	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63685158	CCTGCAGTTTCCACA[A/G]AACACCTCGAGATGT	8925
rs368460721	snp	C/G	0.000167986	0.00916323	missense	HERC1	GRCh38.p7	15:63637611	TGTGCCATTGGCCTG[C/G]ATGACAAAGGTACAA	8925
rs368465677	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63732065	GGAGTGCAGTGGTGC[A/G]ACCTCAGCTCACTTC	8925
rs368471505	snp	C/T	5.16711e-05	0.00508261	synonymous-codon	HERC1	GRCh38.p7	15:63659887	TAATTCAAATTCTTC[C/T]TCACCAGTTAGCTTT	8925
rs368472341	snp	C/T	0.000327946	0.012801	missense	HERC1	GRCh38.p7	15:63616495	TGTTGAGAGTCTGCA[C/T]GTAGAGCAGATCCAC	8925
rs368509534	in-del	-/TA			intron-variant	HERC1	GRCh38.p7	15:63786919	AACTCAATAAATTAT[-/TA]TTTTTTTTTTTTTTA	8925
rs368517086	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63639576	TGTCTGTTTCATATT[A/G]TATCAATGTTTATCC	8925
rs368521189	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63666607	AGAATATGTGGCTGG[A/G]CACTGTGGCTCACAC	8925
rs368527946	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63705434	TTCTTTCTATTCTAA[C/T]TGTAATTAAATGATG	8925
rs368552326	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63662281	GAAGAGTTAATGAAC[A/G]TGACAATCTGTCCTA	8925
rs368559714	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63701932	TAACAATTGAGACTA[A/G]GCCCAATTCTTAATA	8925
rs368571299	in-del	-/CA			intron-variant	HERC1	GRCh38.p7	15:63625125	CAAATCTCACGCATG[-/CA]CACACACACACGCAC	8925
rs368575620	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63744174	TGTGTGTCTCTCTCT[C/G]TCTCTCTCTCTCTCT	8925
rs368581625	snp	A/G	0.000180871	0.00950804	intron-variant	HERC1	GRCh38.p7	15:63634905	TAAGACAGAACCAAG[A/G]AGAAAGAAAATTTTT	8925
rs368591079	snp	C/T	5.50696e-05	0.00524707	synonymous-codon	HERC1	GRCh38.p7	15:63615804	TCGATATTCAATGGC[C/T]CTCTCCACATATTCC	8925
rs368601789	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63745328	TCAGCACTAGGACTC[A/G]CCTAAGAGTTGCAGT	8925
rs368614752	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63628255	AAATTAGCCAGGAAT[A/G]GTAGTGCATGCCTGT	8925
rs368621080	in-del	-/ACAC			intron-variant	HERC1	GRCh38.p7	15:63813311	GATAATCAGAGATGG[-/ACAC]ACACACACACACACA	8925
rs368637538	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63780654	GTGAACCCGGGAGGC[A/G]GAGGTTACGGTGAGC	8925
rs368637553	snp	G/T	0.02016	0.0983543	intron-variant	HERC1	GRCh38.p7	15:63727179	TACTCAGGAGGTTGA[G/T]CCAGGAGAATCACTT	8925
rs368641226	snp	C/T	1.67128e-05	0.00289069	missense	HERC1	GRCh38.p7	15:63749383	TGTCCCTAGGAAGAG[C/T]AGTCCATGCCAGACT	8925
rs368648123	snp	A/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63656852	CTTCAATATTATGTT[A/T]GTAAGATTCATCCAA	8925
rs368663456	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63751076	GACAGTGAAATAATG[C/T]ATACTCAAAATCATC	8925
rs368673285	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63710396	GGCACTTCAATTAAA[A/G]AAAGGAAAAAACCAA	8925
rs368675679	snp	C/T	7.06789e-05	0.00594428	synonymous-codon, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609210	CAGCTGGCTGGAGTA[C/T]GGGGGCAGCCTCAGC	8925
rs368678518	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63670446	AAATGTACTGTCTAC[C/T]AAGTCAGTAATACAA	8925
rs368683020	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63708800	TAGAAGGGTAACATA[C/T]TTCAGCTGGAAAACC	8925
rs368687351	snp	C/T	1.65817e-05	0.00287933	missense	HERC1	GRCh38.p7	15:63775172	GCATCAGTGCTTGAC[C/T]GGGGGCGTTCACTAA	8925
rs368740544	snp	C/G/T	3.4718e-05	0.00416627	intron-variant	HERC1	GRCh38.p7	15:63749341	TGTTAAAACACACAA[C/G/T]AATTTTTAAACATAG	8925
rs368745704	snp	A/G	3.86556e-05	0.00439617	synonymous-codon	HERC1	GRCh38.p7	15:63718643	AAGTAAACGACTTCG[A/G]ACTTTGTATACACAA	8925
rs368748818	snp	A/C	0.000182332	0.00954635	missense	HERC1	GRCh38.p7	15:63749788	CACAGCCCCAAGCAT[A/C]GACCTGAAAAAAACA	8925
rs368755226	snp	C/T	7.04077e-05	0.00593286	intron-variant	HERC1	GRCh38.p7	15:63623912	AAGAAAGGGAGAAAG[C/T]AATGAAATACAACTC	8925
rs368770762	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63720914	CCTTCATTAAAATTA[C/T]GTTCATTTCATACCA	8925
rs368771386	snp	C/G	9.94118e-05	0.00704954	synonymous-codon	HERC1	GRCh38.p7	15:63666411	CCCCATTTCCAGCAA[C/G]GGAACTGCAATTGCT	8925
rs368777434	snp	C/T	0.000167986	0.00916323	intron-variant	HERC1	GRCh38.p7	15:63712771	TGAATCTGGGTATAC[C/T]TACCAGTGCGTAACC	8925
rs368780718	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63778669	GACTTTGCTATATTG[A/T]CTGAAGAGAATGCAA	8925
rs368788542	snp	C/G	4.97839e-05	0.00498893	intron-variant	HERC1	GRCh38.p7	15:63644948	CTCTGATGTCATATA[C/G]TTTCCATAGTTTCAG	8925
rs368821370	snp	C/G/T	0.000860558	0.0207284	intron-variant	HERC1	GRCh38.p7	15:63672730	TAAGAAAGTAGTAAG[C/G/T]ATTTGTTTTTTCAAA	8925
rs368821834	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63798548	ATCTTCAAACTTTAC[-/A]AAAAAAAAAAAAAAA	8925
rs368830666	snp	A/C	1.72829e-05	0.00293959	synonymous-codon	HERC1	GRCh38.p7	15:63713589	AGCTCGAGCCCCAGA[A/C]CCTGCCCCACTGTTC	8925
rs368844126	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63671062	CAAAAAGTTAGCCGG[C/G]AGTGGTAGCACATGC	8925
rs368857560	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63789089	AAAGGTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT	8925
rs368881274	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63772434	CAAAATAAATAGCCC[A/G]TAAAATGAGGAATTA	8925
rs368886333	in-del	-/G			intron-variant	HERC1	GRCh38.p7	15:63690186	AAAAAAAAAAAAAAA[-/G]AAATATTAACCTATT	8925
rs368890647	snp	A/C/T	9.67154e-05	0.00695338	synonymous-codon	HERC1	GRCh38.p7	15:63649858	TGACCAGGCTGTAGC[A/C/T]GGACCCTCTTCTGGC	8925
rs368892000	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63615044	AGCAAGACAGGGAAA[A/G]GGAAATCCATGTGAG	8925
rs368897544	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63710448	AAATAGATTAGACAG[C/T]TATTTATAAATTTAA	8925
rs368906151	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63652941	AGGCATAAGCCACCA[C/T]ACCCAGCCTCCATTC	8925
rs368913039	snp	A/G	2.23937e-05	0.00334609	intron-variant, synonymous-codon	HERC1	GRCh38.p7	15:63654329	CTCCAGAGGGCCTAC[A/G]GCAGAAGGATCATAG	8925
rs368915046	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63682073	CACTAGAACAACCCT[A/G]ATGCATTAGAATATA	8925
rs368940752	in-del	-/C			intron-variant	HERC1	GRCh38.p7	15:63661194	CTGGTATGTAGGTAC[-/C]ACACATGCTTACAAA	8925
rs368947325	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63822028	ACTGTATTCAGTGAA[G/T]ATCTCTCTACAGGGG	8925
rs368962112	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63810642	CTTTTTTTTAATTTA[A/G]AAAAAGGGCAAAGAT	8925
rs368970084	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63809546	GATAATGAAGAGAAA[C/G]AATGGCCAGGACACA	8925
rs368979977	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63703097	CCTGGGCTACAGAGC[A/G]AGACTCTGTCTCAAA	8925
rs368988693	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63758000	GGCGTGAGCCACTGC[A/G]CCCAGCAAAAATTTA	8925
rs368992922	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63777265	TTCACAAGTTTATGA[C/T]TACTATGCTTAATTC	8925
rs369010759	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63790557	CACTCCAGCCTGGGC[A/G]ACACAGCAAGACTCC	8925
rs369029117	snp	A/C	3.95734e-05	0.00444805	missense	HERC1	GRCh38.p7	15:63626055	AAGTGGTAGAGCAGC[A/C]GGAGCCTGGCCCGCA	8925
rs369039465	snp	A/G	0.0002015	0.0100354	intron-variant	HERC1	GRCh38.p7	15:63652397	TTAAATGGTATACAC[A/G]TGATGTTAGCACTCA	8925
rs369058833	snp	C/T	3.32629e-05	0.00407803	missense	HERC1	GRCh38.p7	15:63630608	TTGTGATTGCGAGCA[C/T]GCCCCTCTGGCAAGC	8925
rs369061402	snp	C/T	0.000108707	0.0073717	intron-variant	HERC1	GRCh38.p7	15:63727625	CAAAGGCATTATTTG[C/T]TCTTTTATTGTCTTT	8925
rs369089188	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63616018	ATAACAAACTCACAA[C/T]TTTTAAGGATAAAAA	8925
rs369129996	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63617015	CATTATCTTTTTTTT[C/T]TTTTATTATTATACT	8925
rs369137525	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63672102	AGTTAAAGAAGTATG[C/T]TTAAAATGAAAACAA	8925
rs369142360	snp	C/T	1.6563e-05	0.00287771	synonymous-codon	HERC1	GRCh38.p7	15:63661800	CATGGCTAAGTACTT[C/T]TCCCTGCAGGTGCCA	8925
rs369144643	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63711286	GCAGCCTGAACTCCA[C/G]CCTGAGTGACAGGGT	8925
rs369156361	snp	C/T	4.96931e-05	0.00498439	synonymous-codon	HERC1	GRCh38.p7	15:63733017	GCCGTAAGGTTGATC[C/T]GACAGATTTCCGTAG	8925
rs369197036	snp	C/T	8.91782e-05	0.00667691	intron-variant	HERC1	GRCh38.p7	15:63630674	TGTGGAAATGTTATG[C/T]ACCACACAACACAGT	8925
rs369207929	snp	C/T	0.000163987	0.00905353	intron-variant	HERC1	GRCh38.p7	15:63612221	GCAATAAGGCAGACA[C/T]TACAAAGGAAAAAAG	8925
rs369210511	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63768293	TTGTTAAAATACAGA[A/T]CCTAATCAGTAAGTA	8925
rs369216037	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63828344	GTACAACTTTTTTCC[-/T]TTTTTTTTTTTTAAG	8925
rs369218408	snp	C/T	5.82575e-05	0.00539679	synonymous-codon	HERC1	GRCh38.p7	15:63696304	TTCCATCCCAGACAA[C/T]AGAACGAGGATCTGA	8925
rs369222257	snp	C/T	0.000165986	0.00910854	synonymous-codon	HERC1	GRCh38.p7	15:63642963	CAATATTACCTTTGA[C/T]CTATTTGAGCAAGCA	8925
rs369230581	snp	C/G	3.32701e-05	0.00407847	intron-variant	HERC1	GRCh38.p7	15:63666479	CTGACAAGGCTGAGA[C/G]AAAAGGAAGAGAAAT	8925
rs369238801	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63829559	TGTGTGTGTGTGTGT[A/G]TGTATATATATATAT	8925
rs369288740	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63787130	TACAGGCATGAGCCA[C/T]CATCCCCAGTCTCAA	8925
rs369318344	snp	C/T	4.97789e-05	0.00498868	synonymous-codon	HERC1	GRCh38.p7	15:63640398	AAGGGAAGCCAAGCA[C/T]TGCATATAGGGGCTA	8925
rs369323535	snp	A/G	1.66776e-05	0.00288765	synonymous-codon	HERC1	GRCh38.p7	15:63677865	AGTAATTTCTGCTTC[A/G]TCCCATTGGACCTTG	8925
rs369326772	snp	C/T	3.31274e-05	0.00406972	missense	HERC1	GRCh38.p7	15:63774893	TCAGAAGCTAATCTA[C/T]GACCTAAAGTGTCTG	8925
rs369327928	snp	A/C/T	5.50306e-05	0.00524526	synonymous-codon	HERC1	GRCh38.p7	15:63652425	TCACAATCTGTTGAA[A/C/T]ACACAGGTCTGTTGC	8925
rs369333746	snp	C/T	1.65679e-05	0.00287814	synonymous-codon	HERC1	GRCh38.p7	15:63716405	TTCCATTTCAGCTTC[C/T]TCATCAATAGTTCGA	8925
rs369347117	snp	A/G	0.00034699	0.0131672	synonymous-codon	HERC1	GRCh38.p7	15:63747026	CCCTCCCGCAAGTGC[A/G]AGAGCAAGGTGATTT	8925
rs369387930	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63645249	TACAAGAAATACAAC[C/T]GAGGCCAATATTCTA	8925
rs369391229	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63827895	AGGCACAAAACGCCA[C/T]ATATTATATGATCCA	8925
rs369415367	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63676044	GAGTAGCTGGGATTA[C/T]AGGCGCACGCCACTA	8925
rs369417104	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63745796	TGTCCTTGGCAGGGG[A/G]AATGATCAGTGGAGC	8925
rs369421510	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63721651	CAATAAAAAGTAAAA[A/T]TGTATTTATTTTTGC	8925
rs369423501	in-del	-/ATATATAC			intron-variant	HERC1	GRCh38.p7	15:63737488	TTTTTCCAGATATAT[-/ATATATAC]ATATATATATCTTTT	8925
rs369423885	snp	A/G	0.00015104	0.00868892	intron-variant	HERC1	GRCh38.p7	15:63764090	AAAGCCACGATTATT[A/G]CGTACCTCTTCAAAG	8925
rs369439468	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63688283	GGTGAGGCATCAAGA[C/T]GACTCCTAGGTTTTT	8925
rs369461656	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63639852	AGATGCTAAGATATA[C/T]ACAACTAAAGCACTA	8925
rs369466297	snp	C/T	3.31246e-05	0.00406955	synonymous-codon	HERC1	GRCh38.p7	15:63774949	TTTAAGAAATGTTGT[C/T]ACTTGCGATAAGCAG	8925
rs369468774	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63620299	TTCCATGTAGTTGAG[C/T]GGTTTTGAGTGAGTT	8925
rs369470878	in-del	-/TGTATG			intron-variant	HERC1	GRCh38.p7	15:63829540	ATGTGTGCACATATA[-/TGTATG]TGTGTGTGTGTGTGT	8925
rs369472966	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63803690	TGATAAAATACATTC[C/T]TCCTAACCACTCTTT	8925
rs369478752	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63675435	CTGCAGGGCACACAG[C/T]CTCAGCTGCAACCAC	8925
rs369489198	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63696881	TTCTGCCCCTATCTT[C/T]CCTAGGAAGACACTC	8925
rs369495753	in-del	-/G			intron-variant	HERC1	GRCh38.p7	15:63787983	AAAAAAAAAAAAAAA[-/G]ACAAAACAAAACAAA	8925
rs369498976	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63796415	AACTGAAACCATCTT[A/T]GCAAAATTATGACAG	8925
rs369504007	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63649339	GCCTGGTGACAGAGC[A/G]AGACTCCTTCTCAAA	8925
rs369505314	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63814715	CTCAAGTTATCTGCC[C/T]GCCTCGGCCTCCCAA	8925
rs369525740	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63688025	GAGTATTTTAAGCAG[A/G]GGATGAACATGCTCT	8925
rs369547448	snp	C/T	3.31735e-05	0.00407255	missense	HERC1	GRCh38.p7	15:63658634	CTTAAAGCCACCACA[C/T]GGTCATGAGGGTTTG	8925
rs369574410	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63658125	AACAGCTGTCTTTTA[A/G]GTATTTCTGGTTCTC	8925
rs369581576	snp	A/G	6.80955e-05	0.00583465	intron-variant	HERC1	GRCh38.p7	15:63727879	GGGACAATTGCTTCA[A/G]ATGAACTTTAAAAAA	8925
rs369588349	snp	G/T	0.000134804	0.00820877	intron-variant	HERC1	GRCh38.p7	15:63622792	ATTTTAGACATATAA[G/T]GAACACTTGCTGACT	8925
rs369600989	snp	A/C	0.000124108	0.00787646	intron-variant	HERC1	GRCh38.p7	15:63712929	AAAAAAAGTTTTTTG[A/C]TTTAGGACTGTTAGT	8925
rs369604966	snp	C/T	8.28e-05	0.00643375	synonymous-codon	HERC1	GRCh38.p7	15:63733050	AGTACACACAGAAGA[C/T]AGGTCAGCAGCATCA	8925
rs369611705	snp	C/T	0.000299282	0.0122291	intron-variant	HERC1	GRCh38.p7	15:63661074	ATAAAACAGTTAGTA[C/T]CCCAAGATGCAAATT	8925
rs369623232	snp	A/G	4.30024e-05	0.00463674	intron-variant	HERC1	GRCh38.p7	15:63633828	GTTGTCTGAAAACCT[A/G]GACTCAAGGCAGTAC	8925
rs369623593	snp	C/G			intron-variant, downstream-variant-500B	HERC1	GRCh38.p7	15:63669002	GAATATTTACCAAAA[C/G]AGATGATATTCTAGG	8925
rs369629288	snp	A/C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63714708	TGCGCGCCACCACAC[A/C/T]GGCTAATTTTTTGTA	8925
rs369635073	snp	C/G	6.6246e-05	0.00575488	missense	HERC1	GRCh38.p7	15:63674989	TCTTCATGAACGCCA[C/G]TGAGATATGTTAGGT	8925
rs369636280	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63786805	GGAATTATGAAAATG[C/T]TTTGGAACTAGAGAC	8925
rs369653683	snp	C/T	2.39926e-05	0.00346349	missense	HERC1	GRCh38.p7	15:63655868	TGTTCTCTTCAGCAA[C/T]TCCTCGGAGAAAGCT	8925
rs369672881	snp	A/G	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63666698	GTACTATAAGAGTAT[A/G]TAAATAACCCACTCC	8925
rs369686177	snp	C/T	1.65605e-05	0.0028775	synonymous-codon	HERC1	GRCh38.p7	15:63636012	CCTGGGCCGCCGCTG[C/T]CTGTCGCTGTTCCCA	8925
rs369735447	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63636385	AAGTGATTCTCTTGC[C/G]TCAGCCTCCTGAGTA	8925
rs369752482	in-del	-/CCACAA			intron-variant	HERC1	GRCh38.p7	15:63629673	TCAGTAAGAGTGCAA[-/CCACAA]TGACGAGCAGCTTCC	8925
rs369761338	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63616920	TTCACACAGCACATG[A/G]ACTATATTCTGAACT	8925
rs369765666	snp	C/T	0.00017709	0.00940818	missense	HERC1	GRCh38.p7	15:63694023	TTTTCTTCTTCTTCA[C/T]CGTCTTCTTGCTCCC	8925
rs369774071	snp	C/T	0.00426074	0.0459588	intron-variant	HERC1	GRCh38.p7	15:63747675	ATACACATGCACACA[C/T]GCGCGCGCACACACA	8925
rs369792267	in-del	-/A/AA	0.0676946	0.173323	intron-variant	HERC1	GRCh38.p7	15:63712910	CTGTCTCACATGTAC[-/A/AA]AAAAAAAAAAGTTTT	8925
rs369792899	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63687945	AAGTTGCTTAGACTA[C/T]AGTGAGCAAAAGGGA	8925
rs369801395	snp	C/T	4.96816e-05	0.00498381	synonymous-codon	HERC1	GRCh38.p7	15:63612404	CACCAGCTGATGCTG[C/T]TCATCCACCTCACGG	8925
rs369812892	snp	C/T	0.0287284	0.116357	intron-variant	HERC1	GRCh38.p7	15:63620415	TGCTTTACTTCCAAC[C/T]ATGTGGTCAATTTTG	8925
rs369826618	snp	A/T	9.7745e-05	0.0069902	missense	HERC1	GRCh38.p7	15:63643040	AGCCTATCACAACAG[A/T]TTGCAAGACAGAGCC	8925
rs369834839	snp	A/G	1.65773e-05	0.00287895	missense	HERC1	GRCh38.p7	15:63669544	CACACGCACCTGTGC[A/G]GTTAGCTGGCCTTGC	8925
rs369838996	snp	G/T	1.70452e-05	0.0029193	intron-variant	HERC1	GRCh38.p7	15:63694573	CAAAGAGACAGTTAA[G/T]AATCTTCCTTTCAGT	8925
rs369839128	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63763977	TCTCTAGAGGTAACA[A/G]CTGGTGCCACTTCCT	8925
rs369845019	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63811831	AAAAAAAAAAAAACA[A/G]AAAGGAAAAAACAAA	8925
rs369849810	snp	A/C	1.66488e-05	0.00288515	missense	HERC1	GRCh38.p7	15:63755275	GTATAATTCCCCATC[A/C]TCTGTGACAGCAGCA	8925
rs369893822	snp	C/T	1.66018e-05	0.00288108	synonymous-codon	HERC1	GRCh38.p7	15:63658675	TGCCTGCTCTCCTAA[C/T]GTTATTCTCCCAGAG	8925
rs369910520	snp	C/G/T	8.31934e-05	0.00644911	intron-variant	HERC1	GRCh38.p7	15:63636149	CCACAAAGCCTGGAA[C/G/T]AGAACAGAAACCCAA	8925
rs369910646	snp	A/C/G	3.5033e-05	0.00418513	missense	HERC1	GRCh38.p7	15:63696221	TGCAGCCTCACAGAC[A/C/G]TGAGTAGTGTGGAGG	8925
rs369912556	snp	A/G	6.65491e-05	0.00576803	missense	HERC1	GRCh38.p7	15:63678233	TGCAGTAAGTCCAAC[A/G]GTCTGTTCGGTGAAG	8925
rs369923218	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63754067	TAGTCCCAGCTACTT[C/G]GGGGGCTGAGGCAGG	8925
rs369932267	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63820527	CTGCTTACTTGAATT[A/G]TATCAAATAAAAGTG	8925
rs369933749	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63772997	TTCAACATAATTGGA[C/T]TTTATGAGACACTCC	8925
rs369934238	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63790973	GAAGGCTTGTTTTTA[C/T]GAACATCATTTTAAC	8925
rs369936324	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63636238	CAATCAAAAACCACC[A/G]AATTGGTACTATGAA	8925
rs369940444	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63616250	AAGTGCAGGAGCCTG[A/C]TCTATTAGAAGCTGT	8925
rs369950378	snp	A/G	8.5692e-05	0.00654513	synonymous-codon	HERC1	GRCh38.p7	15:63674649	TGACTTCATAGCACC[A/G]AGGTAAAGATAGGAC	8925
rs369953941	snp	C/T			synonymous-codon	HERC1	GRCh38.p7	15:63616559	GCACAGCTGCTTCCA[C/T]ACCAGAGGGGCCAAG	8925
rs369961418	snp	A/T	1.69284e-05	0.00290928	missense	HERC1	GRCh38.p7	15:63716460	ACATCTGCAGAGTCC[A/T]GGTTTTCTGATATCT	8925
rs369971353	snp	C/T	0.000116687	0.0076374	synonymous-codon	HERC1	GRCh38.p7	15:63775363	CATCTTTGCCAATGC[C/T]AGCTGGCTGCTAAGA	8925
rs369977219	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63704179	CTACTGTGTCAAAGG[A/G]CAGTCACTAAATATA	8925
rs369983037	snp	C/T	7.86009e-05	0.00626851	missense	HERC1	GRCh38.p7	15:63622840	TGTAACCCACTTCTG[C/T]GGTGGCATTGGGAGA	8925
rs370016069	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63671480	TATTCCAGTAAGAGA[C/G]CTAACATGTAGGAGA	8925
rs370042990	snp	C/T	3.31301e-05	0.00406989	missense	HERC1	GRCh38.p7	15:63775035	AGCTCACAACTTCAA[C/T]TGCAGTATGAATGAC	8925
rs370044211	snp	A/C	1.65762e-05	0.00287886	missense	HERC1	GRCh38.p7	15:63661769	TTTCAGAACTTGTTG[A/C]CTTAGATTTGGTCTT	8925
rs370056180	snp	A/C	1.74637e-05	0.00295492	missense	HERC1	GRCh38.p7	15:63675116	ACCAAAAAGTTGGGA[A/C]GCTTTAATAAAGATC	8925
rs370073027	snp	A/G	0.00111231	0.0235567	missense	HERC1	GRCh38.p7	15:63755324	GACACACAAACAACT[A/G]CCTGCATTGCACACA	8925
rs370091268	in-del	-/TGTATATATA			intron-variant	HERC1	GRCh38.p7	15:63829560	GTGTGTGTGTGTGTG[-/TGTATATATA]TATATATATATATAT	8925
rs370121171	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63653233	ATCACCTGAGGTCAG[A/G]AGTTTGAGACCAGCC	8925
rs370131844	snp	C/T	0.000165986	0.00910855	missense	HERC1	GRCh38.p7	15:63680613	TCTCCTTGAGTAAAG[C/T]TGGACAATGTGAGAG	8925
rs370131890	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63727558	TAGCCTTAGGATAGA[-/T]TAGACTCCAATGGAA	8925
rs370144901	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63666210	TTAGGTCTTTATGTT[A/G]TAAGAGTGTTTGCTA	8925
rs370145221	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63714930	ATGGAAGTACAAACT[C/T]TAAAAATTGATCTGT	8925
rs370151527	snp	C/G	0.00242347	0.0347256	intron-variant	HERC1	GRCh38.p7	15:63729447	CCTATCCAAATATCT[C/G]AGTTTCAAGGTCCCT	8925
rs370155552	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63742864	TTTGTTAGTAGTTTG[C/T]TGAGAATTTTTACAT	8925
rs370175935	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63829575	TGTATATATATATAT[A/G]TATATATATATATAT	8925
rs370178810	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63731691	ACTTGTATTGGAAGA[A/G]AAAGAGTACGTAGAC	8925
rs370179945	snp	C/G	3.31884e-05	0.00407346	intron-variant	HERC1	GRCh38.p7	15:63638555	GAAAACCACAATCAT[C/G]TCAAAATTAGAGTCA	8925
rs370186297	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63811628	TCCTGGCTAACATGG[C/T]GAAACCCCGTCTCTC	8925
rs370242279	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63670013	AACTATAATACCAAG[A/T]TAAGAGGGGTAATTT	8925
rs370264437	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63784225	CTTTTTAAGTACCAG[C/T]GGAAAATATTTTCAA	8925
rs370269808	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63800679	ATGGTTTGCAATTAT[A/G]TATAATTTGTGCGAT	8925
rs370270039	in-del	-/AA	0.187917	0.242169	intron-variant	HERC1	GRCh38.p7	15:63696934	TTATCCTTCTTCTTT[-/AA]AAAAAAAAAAAAAAA	8925
rs370277469	snp	A/C	3.33006e-05	0.00408034	intron-variant	HERC1	GRCh38.p7	15:63654095	CATAACGTGATTAAC[A/C]CACTTTCCACTCAAA	8925
rs370301966	snp	C/T	0.000206101	0.0101493	intron-variant	HERC1	GRCh38.p7	15:63637687	TTATTCTTTATTATA[C/T]TGCTTTAACATGCAA	8925
rs370309433	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63645398	CAATAAACTCTTTAA[C/G]ACTACTGAGAAGCCA	8925
rs370317484	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63738993	TTTATTTTTTTTTTT[C/T]CAAATTGACATATAA	8925
rs370337524	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63699944	GACATACTCTCATCA[C/T]TGGTCCATGCATGGC	8925
rs370346330	snp	A/G	0.000216517	0.0104025	synonymous-codon, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609096	TCAGTAGTCAGTGTC[A/G]GAGCCCTCGGCGTTG	8925
rs370351403	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63644741	TCGTCTATCTGTAGT[A/G]TCAATTATATCCACT	8925
rs370357109	snp	A/G	5.5002e-05	0.00524385	missense	HERC1	GRCh38.p7	15:63645489	ACAACATACGTAGCC[A/G]TCAGTAACTGCAACT	8925
rs370359120	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63637454	GTTTGTACGACCAAA[C/T]CTACATTAGGCCTTA	8925
rs370369189	snp	A/G	5.00129e-05	0.0050004	missense	HERC1	GRCh38.p7	15:63674713	TCATGGTTTTTGGAC[A/G]TGTGTTCATGATTTT	8925
rs370373342	snp	C/T	0.000171294	0.00925299	intron-variant	HERC1	GRCh38.p7	15:63658737	AAAAACATAATTCTG[C/T]TTTGTTCTCAACAAG	8925
rs370387535	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63793251	GATGAGACAGGAGGT[C/T]GGCACAAGACACAGG	8925
rs370398610	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63831756	TGCACCCTCTACTAA[A/C]CCAATCCAGTCCAAT	8925
rs370419938	snp	C/T	1.83879e-05	0.0030321	synonymous-codon	HERC1	GRCh38.p7	15:63756683	TCTCCCATAGCTGCC[C/T]TTCCCGCAAGCTCTA	8925
rs370441141	in-del	-/AA			intron-variant	HERC1	GRCh38.p7	15:63809790	CTTGTTTAGAATAGC[-/AA]AAAAAAAAAAAAAAG	8925
rs370443907	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63755796	AAAAAGAAAGAAAGA[A/T]AAGAGAGGAAGAGAG	8925
rs370454719	snp	G/T	3.36604e-05	0.00410232	intron-variant	HERC1	GRCh38.p7	15:63616418	TAGAAACATAGACTG[G/T]CCAGGATTTACCTCA	8925
rs370458744	snp	A/T			missense	HERC1	GRCh38.p7	15:63723355	CAACTCATACATTTA[A/T]CTAAAAAAAATACTC	8925
rs370465670	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63773444	GCTAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	8925
rs370468925	snp	C/G	0.000219633	0.010477	missense	HERC1	GRCh38.p7	15:63641563	TCCCAGAACACCCTG[C/G]TGTTTCAATGCTGTC	8925
rs370489543	snp	A/G	1.78433e-05	0.00298686	synonymous-codon	HERC1	GRCh38.p7	15:63634793	TTTTTTGTTAGAGGT[A/G]TTTCCAAGACCCAGA	8925
rs370492786	snp	A/G	6.17964e-05	0.00555827	missense	HERC1	GRCh38.p7	15:63643484	TAAAGGCAACAGTCC[A/G]AACAGGAGTGATGTG	8925
rs370495490	snp	C/T	0.000665004	0.0182225	intron-variant	HERC1	GRCh38.p7	15:63672467	ACACAGGCATCAGTA[C/T]GGCAGACATTAAAGG	8925
rs370508068	snp	C/G	0.00605347	0.0546817	intron-variant	HERC1	GRCh38.p7	15:63652370	ATGAGGCATGTTTAG[C/G]ATTCTCTTATTTTAA	8925
rs370520782	snp	C/T	3.31351e-05	0.00407019	missense	HERC1	GRCh38.p7	15:63713419	TGTCCTTCTTCTCTT[C/T]GCTTCTGAAGCTCAT	8925
rs370548000	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63747923	TATGCACGATCAAAA[A/T]CGAAAATTAAAACAT	8925
rs370553306	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63770078	AGTCCCCAAAGCCTA[C/T]AGCATGGGATACAGG	8925
rs370557168	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63788555	ACTTAATGAAGCACA[A/G]AAAGTACAGCTGTAA	8925
rs370560212	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63672852	AAAAAAATATTCTTA[C/G]TTATATACATCTTTG	8925
rs370584422	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63679167	AGCACCAGGCCATCA[C/T]TCGAACCAGAACATG	8925
rs370605686	snp	C/T	3.49058e-05	0.00417752	missense	HERC1	GRCh38.p7	15:63645510	AACTGCAACTTGGAT[C/T]CTTTCCCTGGAAGGC	8925
rs370606413	snp	C/T	1.65869e-05	0.00287979	missense	HERC1	GRCh38.p7	15:63616459	CCTCGGTAATCCCAC[C/T]GTCTTCAATGTGAAG	8925
rs370627508	snp	A/G	1.65985e-05	0.00288079	missense	HERC1	GRCh38.p7	15:63674771	GGGATTCCACACTTG[A/G]CAGTGTTGGATCTAA	8925
rs370630668	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63812869	ATTCCTAGATTCGAA[A/G]ACTAAATATTATAAA	8925
rs370631768	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63724282	GGAATTATCTTTATC[A/T]TGTTAAAGACCCCTT	8925
rs370637638	snp	C/T	0.00716266	0.059414	intron-variant	HERC1	GRCh38.p7	15:63634041	CCGTTTCTGGGACCC[C/T]TTTTCTCTACTTCAG	8925
rs370646277	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63639049	ACCCACAGGTACAAG[A/G]TCATGTGGAGGACCC	8925
rs370651981	snp	C/T	5.04257e-05	0.00502099	missense	HERC1	GRCh38.p7	15:63775560	ATTCACTGTCCTCTG[C/T]AATCCAGGAGCTGTT	8925
rs370682923	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63647025	TTTGGGAGGCTGAGG[C/T]AGGTGGATCACTTGA	8925
rs370713627	snp	C/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63747197	AGGTGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	8925
rs370728248	snp	A/C	0.000256746	0.0113273	intron-variant	HERC1	GRCh38.p7	15:63656362	CAACTGGAACCACTG[A/C]CAGTAAAGAAAAACA	8925
rs370736461	snp	C/G/T	0.000100204	0.00707766	synonymous-codon	HERC1	GRCh38.p7	15:63725314	AGGAGTGTCCATTTC[C/G/T]ACACCGTCACTGAAC	8925
rs370739679	snp	A/G	8.31248e-05	0.00644636	intron-variant	HERC1	GRCh38.p7	15:63623704	CTAGATAACTCAGCA[A/G]GGGACACTGCAGGAA	8925
rs370753889	snp	A/C	0.000167986	0.00916323	intron-variant	HERC1	GRCh38.p7	15:63729474	CCCTGATAGATCACC[A/C]TAAAAGACAAATAAT	8925
rs370758973	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63816451	TCAAGTTCATGCTGA[C/G]AAATCTGGCTCAAGA	8925
rs370761354	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63830989	CAAACTTCTCTGTAA[A/G]TGATTTGACCAACTT	8925
rs370776298	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63632127	AATTCCTTACCCTTC[C/T]CCACAAACCAGCTCA	8925
rs370785502	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63780677	CGGTGAGCCAAGATC[A/G]TGCCACTGCACTCCA	8925
rs370786286	snp	C/T	0.000157987	0.00888643	synonymous-codon	HERC1	GRCh38.p7	15:63623755	GATGGTGTCATCAAA[C/T]ACTCCTCCAGCATCA	8925
rs370789001	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63650450	AGAGGGTCTTGCTGT[A/G]TTGCCCAGGTTGGAG	8925
rs370790860	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63613966	CGAACAAGCTGTTAT[G/T]CTTGGTGGAACACAA	8925
rs370792299	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63661674	AATGTAACTCCTCAC[A/G]TGAAAAATCTACAGT	8925
rs370797485	snp	C/T	3.3888e-05	0.00411617	intron-variant	HERC1	GRCh38.p7	15:63640130	CTCAGCTGCAAATAA[C/T]AGCAGCTCACAGTAC	8925
rs370807057	snp	C/T	0.000207641	0.0101871	synonymous-codon	HERC1	GRCh38.p7	15:63718595	GTCCCGTGATGATGA[C/T]CTTGTTTGAATAAGT	8925
rs370807343	snp	G/T	0.000167986	0.00916324	missense	HERC1	GRCh38.p7	15:63749454	TCTAAGCCACTCACT[G/T]TCTTTGGTTTAGTAA	8925
rs370809691	snp	C/T	0.000228549	0.0106875	missense	HERC1	GRCh38.p7	15:63649757	TGCTCCAATTCTCGA[C/T]GGTGCATGGTGGACA	8925
rs370815220	snp	C/T	0.000296041	0.0121628	intron-variant	HERC1	GRCh38.p7	15:63686330	GACTAAAAGACAAAA[C/T]GCTAAAAACTATTAG	8925
rs370817523	snp	A/G	3.31274e-05	0.00406972	synonymous-codon	HERC1	GRCh38.p7	15:63677925	CAGCAGCGTGGCATG[A/G]CGCCCAGTTTGCTTG	8925
rs370817607	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63744597	GCCTCCCCTTTCCAA[A/G]GCTAGAGGAGCCTCG	8925
rs370821727	snp	A/C	1.65594e-05	0.0028774	missense	HERC1	GRCh38.p7	15:63661951	TTCATGTGCTGATTG[A/C]AGCTGACGACGCTGC	8925
rs370838548	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63806165	GCAGAACACAAGTGG[-/T]TTTTTTTTTTTTCTC	8925
rs370877440	snp	C/G	1.73456e-05	0.00294491	missense	HERC1	GRCh38.p7	15:63634881	GAGTGCTTGAAGCCA[C/G]AAGACATCTAAGACA	8925
rs370879021	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63816839	AATAATAGAATTTCA[C/T]AATTTTGCAATCACT	8925
rs370890182	snp	A/G	0.00131136	0.0255727	synonymous-codon	HERC1	GRCh38.p7	15:63637641	ATTCTGACCACAAAT[A/G]ACCTAGTATAAAAAC	8925
rs370905411	snp	A/G	2.07699e-05	0.00322251	synonymous-codon	HERC1	GRCh38.p7	15:63659932	ATCCAACATGTCCCA[A/G]TCTTCTGGAATTTAA	8925
rs370910789	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63743234	TTGTCTCCTCTGTGT[A/T]TTTTCTTTTTTTTTC	8925
rs370911563	snp	C/T	3.52361e-05	0.00419724	intron-variant	HERC1	GRCh38.p7	15:63680518	GAAAAATGTAATGCT[C/T]GTGAATGGGTGTCGG	8925
rs370911755	snp	A/C/G	1.7532e-05	0.00296069	missense	HERC1	GRCh38.p7	15:63645565	TAGATGGATGGCAGA[A/C/G]TGAATGTAGACAGCA	8925
rs370917119	snp	A/G	1.66944e-05	0.0028891	missense	HERC1	GRCh38.p7	15:63698799	ACATACTTTCCTCTG[A/G]CTCTTTAAAACCTGG	8925
rs370917159	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63752328	ACTTTTTTACTGCCA[-/T]TAACTGATGGATACA	8925
rs370921477	snp	C/T	1.70624e-05	0.00292077	missense	HERC1	GRCh38.p7	15:63713582	GATCATCAGCTCGAG[C/T]CCCAGACCCTGCCCC	8925
rs370923299	snp	A/G	0.00013844	0.00831871	missense	HERC1	GRCh38.p7	15:63764145	GAGCACAAGCCATCC[A/G]ATGTTCTGGTTGGTT	8925
rs370925074	snp	C/G	0.00920423	0.0672116	intron-variant	HERC1	GRCh38.p7	15:63622897	TTTCAAGTTCCTGCA[C/G]AAGAAAGAAAAAAAT	8925
rs370937975	snp	G/T	3.31411e-05	0.00407056	missense	HERC1	GRCh38.p7	15:63775128	CAAATAATAAACTTA[G/T]ACCAGTTCGAACACC	8925
rs370960151	snp	A/G	3.41326e-05	0.004131	synonymous-codon	HERC1	GRCh38.p7	15:63641479	AGTTACCTTTTCATA[A/G]GCATACTGCTCCTGA	8925
rs370968271	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63831985	AAATGATAAGAACCT[C/T]AGGGAACGCAAAATT	8925
rs370974737	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63658987	AGTATTTTCTGTTTT[G/T]TTCATTTTGCCCATG	8925
rs370977063	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63707651	TGACAAAACAAGGCC[A/G]GGAGTGGTGGCTCAC	8925
rs371027988	snp	C/T	1.65704e-05	0.00287836	synonymous-codon	HERC1	GRCh38.p7	15:63756539	CCAACTGAAGACTTC[C/T]CCTTCTGTCGTAAAG	8925
rs371084973	snp	C/T	0.000167986	0.00916323	missense	HERC1	GRCh38.p7	15:63694813	GGGCTCTTTCCAGGG[C/T]AGCAGACAACTGTTG	8925
rs371089836	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63808673	TCAACAGTCTGTTAC[A/G]GTAATAGATACAATT	8925
rs371099050	snp	A/G	0.000117141	0.00765225	missense	HERC1	GRCh38.p7	15:63672571	GTGACTGGAGTGGTG[A/G]CAGTTGTGGTGTCCT	8925
rs371099070	snp	A/G	0.00047866	0.0154629	intron-variant	HERC1	GRCh38.p7	15:63756395	GTCAATTACAACTCC[A/G]ATGCATCTAATTATT	8925
rs371132233	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63618026	TAGATCCCATTTGTC[A/T]ATTTTGGCTTTTGTT	8925
rs371132792	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63776555	ATACTTCAATCAAAA[C/T]AGTGGTTGCCTCTAG	8925
rs371141561	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63665390	TACAAAAAATGAGCC[G/T]GGCATGGTGGCACAT	8925
rs371144516	snp	A/C	3.37747e-05	0.00410928	intron-variant	HERC1	GRCh38.p7	15:63662042	CAAAAGGATTTCATA[A/C]CAAATGATTAGTCAA	8925
rs371144797	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63646172	AATCCTCTTCCACAT[A/C]TTCTAACTCCTGGTT	8925
rs371150754	snp	A/G	1.90503e-05	0.00308623	stop-gained	HERC1	GRCh38.p7	15:63696141	GATAGTGATGCAATC[A/G]GCCACTCTCTCCCTT	8925
rs371152056	snp	A/G	0.000159987	0.00894249	synonymous-codon	HERC1	GRCh38.p7	15:63678048	CAGCTCTGAGAGGTC[A/G]GCGAGGCCATGCCTA	8925
rs371152480	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63822343	GCAATCCCAGCACTT[C/T]GGGAAGCCGAGGCGG	8925
rs371163845	snp	C/T	6.62515e-05	0.00575512	missense	HERC1	GRCh38.p7	15:63725408	ATGCCACCAAGACAC[C/T]GCCCAATAAGGAGAG	8925
rs371180338	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63826887	TTCACACATTACTGG[C/T]GAGAATGCAAATTGG	8925
rs371187803	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63741262	TCGAACTCCTGACCT[C/T]GTGATCCACCCGCCT	8925
rs371189714	snp	G/T			upstream-variant-2KB, utr-variant-5-prime	HERC1	GRCh38.p7	15:63833961	GACGTAAGAGGCGGC[G/T]GCAGCAGCGGCGGCG	8925
rs371190398	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63765639	TCTTTCAACGAACGG[C/T]CAATCAGAATATGTT	8925
rs371192259	snp	A/C/G	3.5173e-05	0.00419351	intron-variant	HERC1	GRCh38.p7	15:63623914	GAAAGGGAGAAAGCA[A/C/G]TGAAATACAACTCTT	8925
rs371200954	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63744170	TGTGTGTGTGTCTCT[C/G]TCTCTCTCTCTCTCT	8925
rs371201509	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63801590	CTTATATCCCTAGTG[C/T]TTATTAGCATAGGTA	8925
rs371202758	in-del	A/TACG			intron-variant	HERC1	GRCh38.p7	15:63739878	TGGACTTACACAATA[A/TACG]GCCCTTTGTGTCTGG	8925
rs371241903	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63673215	TTTACAAAGTATTTA[C/T]ATATTTTTTTTAATT	8925
rs371244791	snp	A/G	0.000116454	0.00762978	missense	HERC1	GRCh38.p7	15:63630609	TGTGATTGCGAGCAC[A/G]CCCCTCTGGCAAGCC	8925
rs371248637	snp	C/T	6.20328e-05	0.00556889	missense	HERC1	GRCh38.p7	15:63645618	CAGAGTTTCACACTG[C/T]CTTCTTTGGCACATG	8925
rs371254434	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63824459	GAATCACTTGAACCC[A/G]GGAGGCAGAGGTTGC	8925
rs371254677	snp	A/G	4.60649e-05	0.00479899	intron-variant, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609301	GCCGTGACTGGGGAC[A/G]TCAGAGTGCCATAAG	8925
rs371256403	snp	C/G/T	0.00013261	0.00814191	missense	HERC1	GRCh38.p7	15:63674866	GATGTTAGGCCTGTT[C/G/T]GCATATCTAAAGCGG	8925
rs371258430	snp	A/T	0.000217812	0.0104335	intron-variant	HERC1	GRCh38.p7	15:63660947	AAAAAAACATGTAAA[A/T]TAAAGAAGCTCTCAA	8925
rs371264866	snp	A/G	0.000781178	0.0197479	synonymous-codon	HERC1	GRCh38.p7	15:63694478	CAGTGGAAATTGCCA[A/G]AGAAACATCTACTGG	8925
rs371273063	snp	A/G/T	0.000122102	0.00781268	missense	HERC1	GRCh38.p7	15:63718672	AACGGTACACTTCTG[A/G/T]TAAGTGTTTACCAGG	8925
rs371276055	snp	G/T	0.0232847	0.105357	intron-variant	HERC1	GRCh38.p7	15:63618855	GATTTTGTATCCTGA[G/T]ACTTTGCTGAAGTTG	8925
rs371280204	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63655599	TTTCCATACACAGTG[A/T]AAAAGTATCTATGCA	8925
rs371285022	snp	A/G	0.000167825	0.00915883	intron-variant	HERC1	GRCh38.p7	15:63752923	CTAATCCTCTGAAAT[A/G]CTCTAAGTCTTTTAT	8925
rs371298119	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63754769	ATTTTTTTAATGCAA[C/T]GCAATATGAAAAACA	8925
rs371315853	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63766074	AACTCACTATAGCCT[C/G]AACCTCCTGGGCTCA	8925
rs371321874	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63786516	AAATGACCATCAAGA[C/T]ATGAATGAATAAACA	8925
rs371344772	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63795034	TTGTGCCACTGCATT[A/C]CAGCCCGGGCAACAG	8925
rs371347023	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63762475	ATTACAGACGTCTGC[C/T]GCCCCACCCAGCTAA	8925
rs371360684	snp	C/T	2.56934e-05	0.00358414	missense	HERC1	GRCh38.p7	15:63652495	GTGCCATCATTGCCA[C/T]TTGTAGCCAAAAGAC	8925
rs371365901	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63789094	TTTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTTTG	8925
rs371382538	snp	A/G	1.80188e-05	0.00300151	synonymous-codon	HERC1	GRCh38.p7	15:63633886	AATTTCCTAAGCCTA[A/G]TTTTCCATAGTCTCC	8925
rs371389261	snp	C/T	1.6591e-05	0.00288015	synonymous-codon	HERC1	GRCh38.p7	15:63674793	TGGATCTAAAGAAAA[C/T]GAAGCGATTTCATTT	8925
rs371402167	in-del	-/AT	0.316485	0.240998	intron-variant	HERC1	GRCh38.p7	15:63829464	TGTGTGTGTGTGCAC[-/AT]ATATGTTTATATAAA	8925
rs371404887	snp	A/G	0.000132672	0.00814362	synonymous-codon	HERC1	GRCh38.p7	15:63775192	GCGTTCACTAACAGA[A/G]TGGACATCTGCTGAA	8925
rs371407529	snp	A/C	4.37206e-05	0.0046753	missense	HERC1	GRCh38.p7	15:63718627	CAAGGTTCTTGCAAG[A/C]AAGTAAACGACTTCG	8925
rs371409376	snp	A/G	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63671069	TTAGCCGGGAGTGGT[A/G]GCACATGCCTGTAAT	8925
rs371426462	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63646830	AACAAACAAACAAAC[A/C]AAAACAAAAACAAAA	8925
rs371439806	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63828353	TTTTTCCTTTTTTTT[C/T]TTTAAGACAAAGTTT	8925
rs371443027	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63819371	ACATCAATTGAGAAA[A/T]TGTTTACAAAAGTAT	8925
rs371464139	snp	C/T	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63614244	TCAGAAAAGCCTGGA[C/T]ACCATCTTAGAGCCT	8925
rs371469130	snp	C/G	0.000351085	0.0132446	intron-variant	HERC1	GRCh38.p7	15:63638399	TTTTCTATTTTTTAT[C/G]CTGTTAGTTACCTGT	8925
rs371470472	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63636490	TGGCCAGGCTGGTCA[C/T]GAACTCCTGACCTCA	8925
rs371477245	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63635117	CAGTGGTGTGATCAC[A/G]GCTCACTGCAGCCCC	8925
rs371486775	in-del	-/AT	0.0611083	0.163768	intron-variant	HERC1	GRCh38.p7	15:63737373	ATATCTTTTTTCCAG[-/AT]ATATATATATATATA	8925
rs371487997	snp	C/G	0.000617809	0.0175648	intron-variant	HERC1	GRCh38.p7	15:63628626	CAGACAGTGCCATGG[C/G]GTACTGCTAAAAAAG	8925
rs371521135	in-del	-/A/AA/AAA	0.473359	0.112298	intron-variant	HERC1	GRCh38.p7	15:63671203	GTGAAACTTTGTCTC[-/A/AA/AAA]AAAAAAAAAAAAAAA	8925
rs371527327	snp	C/T	6.65048e-05	0.00576611	missense	HERC1	GRCh38.p7	15:63674441	CAGCTAATCCCAATG[C/T]TCTCTTTATGGGTGA	8925
rs371529585	in-del	-/C			intron-variant	HERC1	GRCh38.p7	15:63625286	AAGTATCTGAAATTT[-/C]TCAGATTAATTTATG	8925
rs371532854	snp	C/T	0.000601167	0.0173269	intron-variant	HERC1	GRCh38.p7	15:63692589	GAAGAGACAAGTTTA[C/T]GTTACAACCAAGAGC	8925
rs371576830	snp	C/T	2.2566e-05	0.00335894	missense	HERC1	GRCh38.p7	15:63615866	TTCCACCAGGGATTA[C/T]AGGAACCATTTTGCC	8925
rs371579039	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63618695	GAGCAGTGGTTTGTA[C/G]TTCTCCTTGAAGAGG	8925
rs371581302	snp	C/G	6.62855e-05	0.00575659	missense	HERC1	GRCh38.p7	15:63640193	GAACAGGTTCTAGAT[C/G]TGGAACGGTAAAAGA	8925
rs371582209	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63693477	TTGAACTCCTGGGCT[C/G]AAGCAATCCACCCAC	8925
rs371585821	snp	C/G	3.31378e-05	0.00407036	missense	HERC1	GRCh38.p7	15:63663169	CTTCTCTCCGACTTT[C/G]ATTCCTGTGGGCCTG	8925
rs371586985	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63743298	AATGGAGTCTCACTC[C/T]GTCACCAGGCTGGAG	8925
rs371592802	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HERC1	GRCh38.p7	15:63668881	GACAAAAAAACCAGA[A/G]AGGATAAAGAAGACT	8925
rs371608092	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63756269	TAAGAATTAAAATTC[A/C]ATAATGTATACAAAG	8925
rs371611239	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63799133	CAAAATTATAAACTC[C/T]GTAGCTTAGCAGAGA	8925
rs371623414	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63626662	ATGAGGCTTTTACTA[A/C]AAGAATAAGAGTTCT	8925
rs371632027	snp	A/G	1.65886e-05	0.00287993	intron-variant	HERC1	GRCh38.p7	15:63733167	AACAATAAAATAGGA[A/G]CAAGTAACTAGCGTA	8925
rs371633991	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63654800	CTTCAAGCTGGGAGA[C/T]GGAGGTTGCGGTGAG	8925
rs371690640	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63779290	TTAACCCAGACAATC[A/G]ACTCCAAGAAATAGC	8925
rs371704393	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63652652	ATTAAAAGAAAAGCA[A/T]CCATTCCTTTCTTTT	8925
rs371710233	snp	C/G	1.65655e-05	0.00287793	synonymous-codon	HERC1	GRCh38.p7	15:63674910	TTTCTGCTCAACATC[C/G]CCTTTCTCCTCGGAT	8925
rs371715992	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63634397	TGTTGCAATTCAGCC[A/G]TACAACTCAAGGATA	8925
rs371731267	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63661515	GGGTCCTGACCATTA[C/T]TTGCCAACAAGTCAG	8925
rs371733328	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63614509	ACTGACAAGACCCAA[C/T]TTCACTAGGCTAAAG	8925
rs371734643	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63740641	GAAGTGGTATCTCAG[G/T]GTGGTTTTGATTTGT	8925
rs371768176	snp	C/G/T	8.42657e-05	0.0064905	synonymous-codon	HERC1	GRCh38.p7	15:63712829	ATCAGATTCACTCCT[C/G/T]GATTTGATCAGTCTA	8925
rs371769862	snp	A/C			upstream-variant-2KB	HERC1	GRCh38.p7	15:63834082	GAACCGAGAGGAAGG[A/C]GGCTGAGGTGGAGTT	8925
rs371772189	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63720072	AATCACAACATTAGA[C/T]GATGAGGACTAGTCA	8925
rs371777048	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63615091	TTGAAGGTTCATTTA[C/T]GTGGGCCCTGACTAA	8925
rs371805279	snp	A/C/T			intron-variant	HERC1	GRCh38.p7	15:63726687	AAAGAATGAGAATTG[A/C/T]CAGAGTCTGTCTACA	8925
rs371815708	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63770792	CCAGTTACTCAAGGA[C/T]AGAGAAATTCAAGAC	8925
rs371818682	snp	C/G	0.000102921	0.00717287	intron-variant	HERC1	GRCh38.p7	15:63616710	AGGGAATATTTCAAA[C/G]AGCATTTTCCTTATT	8925
rs371833352	snp	C/T	0.000167986	0.00916323	synonymous-codon	HERC1	GRCh38.p7	15:63648120	AAGTGGTTCCTTTGT[C/T]CCCAGTAACAGTTTT	8925
rs371842557	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63616141	TCTCTGTTCACAAAC[C/T]AAGCCTGTTGAACTC	8925
rs371853982	snp	C/G	1.66158e-05	0.0028823	missense	HERC1	GRCh38.p7	15:63616552	GGACACAGCACAGCT[C/G]CTTCCACACCAGAGG	8925
rs371854665	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63829075	GTTAGAATGAACTTT[A/G]TGGTACTGGATTAGA	8925
rs371859723	snp	A/T	0.000165986	0.00910854	missense	HERC1	GRCh38.p7	15:63624168	CTAACCTGGTTGATA[A/T]CCTCTTTACAGTTAT	8925
rs371867701	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63653198	GTAATCCCAGCACTG[C/T]GGGAGGCCAAGGCAG	8925
rs371871759	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63624471	GGAGGCTGTGGTGGG[C/T]GGATCGCTTGAGCCC	8925
rs371899394	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63794285	ACTCGCCCTGAATTC[G/T]TTCTTGCGTGAGATC	8925
rs371907058	snp	A/C/G/T	0.000919235	0.0214238	intron-variant	HERC1	GRCh38.p7	15:63747099	CTGAAACCAAATAAA[A/C/G/T]GTCTATGAATTCTCG	8925
rs371913879	snp	A/G	8.31843e-05	0.00644866	synonymous-codon	HERC1	GRCh38.p7	15:63775333	TGCCCCGGCAAATGG[A/G]GAATCTGAACATACC	8925
rs371976999	snp	C/G	0.000175985	0.00937878	intron-variant	HERC1	GRCh38.p7	15:63649972	CTTAATTCTTAAAAA[C/G]AAAAAAAGGAACAGA	8925
rs371979138	snp	A/C/T	3.31566e-05	0.00407154	synonymous-codon, missense	HERC1	GRCh38.p7	15:63678060	GTCAGCGAGGCCATG[A/C/T]CTAGTATGTTTACCT	8925
rs371995366	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63751133	AGGTATCATATACAC[G/T]CATGCACCATTCGGT	8925
rs372004432	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63705985	CAGTGAGCTATGATG[A/G]TGCCACTGCACTCCA	8925
rs372010338	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63757457	ATTTTAGTAGAGACG[A/G]GGTTTCACCATGTTG	8925
rs372038815	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63629932	GGTGAATACATCAAC[C/G]TCTTGAGTCTCTTAT	8925
rs372075398	snp	A/C	1.68289e-05	0.00290072	missense	HERC1	GRCh38.p7	15:63755319	CAGCTGACACACAAA[A/C]AACTACCTGCATTGC	8925
rs372122413	snp	A/C/T	3.35639e-05	0.00409647	splice-acceptor-variant	HERC1	GRCh38.p7	15:63694550	GACGTTGCTGGGCTT[A/C/T]TAAAAGACAAAGAGA	8925
rs372138455	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63708582	ACAGTTAAACTTAGG[G/T]TTGGTATTCTCTGTT	8925
rs372144787	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63676572	GACCAACCTGGGTAA[C/T]ATGGTGAAACCCTGT	8925
rs372163435	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63819276	GGGGCTCATTCCTAA[A/G]GCAGCTCCCTCTCTC	8925
rs372164069	snp	A/G	1.71231e-05	0.00292597	synonymous-codon, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609144	CATGTAGTTGTCCAT[A/G]TCGATTGAGCGGCAG	8925
rs372167948	snp	C/T			downstream-variant-500B, utr-variant-3-prime	HERC1, FBXL22	GRCh38.p7	15:63608454	TTCTCTGATACGTTA[C/T]TTCCAAGTGAAGCCC	8925
rs372178578	snp	A/G	1.81989e-05	0.00301647	synonymous-codon, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609237	CAGCTGGAAGAAGCA[A/G]GTCTGTGAGGTAGGC	8925
rs372181076	snp	C/T	0.000167986	0.00916323	missense	HERC1	GRCh38.p7	15:63641631	CTGCTGTACAATTCA[C/T]GACCAAAACATCCTG	8925
rs372191034	snp	C/T	0.000167986	0.00916322	missense	HERC1	GRCh38.p7	15:63666368	TACCTGTAGCTTCCA[C/T]GGCTTTGGCAATCTG	8925
rs372198548	snp	A/G	2.72982e-05	0.00369437	missense	HERC1	GRCh38.p7	15:63641573	CCCTGCTGTTTCAAT[A/G]CTGTCCTACAGGTTG	8925
rs372201050	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63625607	GCTGAGGCAGGAGAA[C/T]TGCTTGAACCCAAGA	8925
rs372226906	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63810545	AATGAAGATACAGTA[C/T]GAATGAATGAAAGGG	8925
rs372232724	in-del	-/CCT			upstream-variant-2KB	HERC1	GRCh38.p7	15:63835445	CAAGCAAAAGCTCCT[-/CCT]TTTAACTTGTTGATG	8925
rs372244251	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63787995	AAAGACAAAACAAAA[A/C]AAAAAACCTTACAAG	8925
rs372257132	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63757257	GAAATTCCAGTTTTT[A/T]TTTACTTTTTTTTTT	8925
rs372268673	snp	A/C/G	3.31945e-05	0.00407383	missense	HERC1	GRCh38.p7	15:63638434	CCTGTGAGAATGAGG[A/C/G]AGCTGCTGCAGGTAC	8925
rs372304757	snp	C/T	3.80394e-05	0.00436099	missense	HERC1	GRCh38.p7	15:63713614	CTGTTCATTCTATCT[C/T]GGTCTCGGCTACGAG	8925
rs372306188	snp	C/G/T	9.93648e-05	0.00704795	missense	HERC1	GRCh38.p7	15:63640253	CTTCGGCAGCTTTTA[C/G/T]AGTGGTTGAGAAACA	8925
rs372308270	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63770931	CGGTGGCTCACGCCT[A/G]TAATCCCAGCACTGT	8925
rs372316431	snp	C/T	4.97162e-05	0.00498554	missense	HERC1	GRCh38.p7	15:63624230	GTTTTTCCTATGGAG[C/T]GCACCATTGGCAGAG	8925
rs372318271	snp	C/G	1.66852e-05	0.0028883	missense	HERC1	GRCh38.p7	15:63651367	ATCCCAGGCTTTCCT[C/G]AGCATCCCCTTCCCT	8925
rs372318960	snp	C/T	1.65811e-05	0.00287929	missense	HERC1	GRCh38.p7	15:63775185	ACCGGGGGCGTTCAC[C/T]AACAGAATGGACATC	8925
rs372330999	snp	A/C	0.000167986	0.00916323	intron-variant	HERC1	GRCh38.p7	15:63664434	CTTTCAAAATAAGAT[A/C]TTTCACAAAGAAAAG	8925
rs372333684	snp	A/C/T	2.01485e-05	0.00317393	missense	HERC1	GRCh38.p7	15:63713626	TCTCGGTCTCGGCTA[A/C/T]GAGCTACTTCACGGG	8925
rs372338210	snp	A/G	0.000161987	0.00899818	missense	HERC1	GRCh38.p7	15:63696209	CCTGCTAGGAACTGC[A/G]GCCTCACAGACGTGA	8925
rs372344740	snp	C/T	1.67416e-05	0.00289318	intron-variant	HERC1	GRCh38.p7	15:63635922	TCAACAACTAGTATA[C/T]TTACAATGAAAGGCA	8925
rs372353470	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63631937	CTCTCTCTCTCTGGG[-/T]TTTTTAGATGATACG	8925
rs372357333	snp	C/G	2.07471e-05	0.00322073	missense	HERC1	GRCh38.p7	15:63615842	TGGAAAATGTGAGTG[C/G]GATACTATTTCCACC	8925
rs372359436	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63702573	TTCTGTAAACAATCG[A/T]ACAACCATAGCAAAT	8925
rs372360705	in-del	-/ATC			intron-variant	HERC1	GRCh38.p7	15:63640029	GAAAAATATTTTCCA[-/ATC]TTTCTCTTAAGGGTA	8925
rs372365920	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63680436	GAGAGAAAGGAGAGA[C/T]GAGCAGATAATCTAT	8925
rs372429637	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63767471	TTGGGAGGCCAAGGC[A/G]GGTGGATCATCTGAG	8925
rs372444165	snp	A/T	0.000221104	0.0105121	intron-variant	HERC1	GRCh38.p7	15:63652375	GCATGTTTAGGATTC[A/T]CTTATTTTAAATGGT	8925
rs372447733	snp	C/G/T	0.000105692	0.00726885	intron-variant	HERC1	GRCh38.p7	15:63624377	AATCTAGGCTTAAAA[C/G/T]AAATAACAATTTTCA	8925
rs372447795	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63610949	TACCCAGTGTTCAGG[A/T]GGTGGAGAGAAGGAG	8925
rs372453196	snp	G/T	0.000614133	0.0175126	intron-variant	HERC1	GRCh38.p7	15:63733178	AGGAACAAGTAACTA[G/T]CGTAATATGCACTAG	8925
rs372512998	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63833508	GCCGGGGCACAGACG[G/T]TGTAAGCCGCTGGAG	8925
rs372516618	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63686997	TAAAGACAAGCAGCA[C/T]GTAATGACTGGAAGA	8925
rs372520163	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63648484	ATTAAATTCCTTTGC[G/T]GATTGTAAGTCACCA	8925
rs372528904	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63786869	CCACTAAATCGCTCA[C/T]TTTAAGATGGTTAAT	8925
rs372540459	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63698245	ACATGGTGAAACTTT[A/G]TCTCTCCTAATAATA	8925
rs372555771	snp	C/T	0.000265318	0.0115147	intron-variant	HERC1	GRCh38.p7	15:63638669	TTTAGAATCAAAACA[C/T]TGACTGAGAACCATC	8925
rs372560582	in-del	-/AT	0.000190224	0.00975069	intron-variant	HERC1	GRCh38.p7	15:63630658	AAACAAAACAAAAAC[-/AT]GTGGAAATGTTATGC	8925
rs372579756	snp	C/G			downstream-variant-500B, utr-variant-3-prime	HERC1, FBXL22	GRCh38.p7	15:63608403	CAATGGAAAATAGGG[C/G]CTTCCAACCCAGAGG	8925
rs372581032	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63626462	AGGCAGTTCTTTCAC[A/G]AAAATAAAGCCAAAT	8925
rs372589572	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63703109	GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	8925
rs372596416	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63654699	CTCTACTGAAAATAC[-/A]AAAAAAAAAAAAAAT	8925
rs372596939	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63658746	ATTCTGTTTTGTTCT[C/T]AACAAGGTAAGAAAA	8925
rs372604267	snp	C/T	0.000169986	0.00921758	missense	HERC1	GRCh38.p7	15:63689689	AGAAGGGAAAATAAG[C/T]GCTCAACAATCTGTT	8925
rs372626972	snp	C/G	0.00011922	0.00771984	missense	HERC1	GRCh38.p7	15:63648152	CATCAAAATATCCCA[C/G]TGCAAATGGTCTGTC	8925
rs372635208	snp	A/G	3.31296e-05	0.00406985	synonymous-codon	HERC1	GRCh38.p7	15:63729532	GGCAAAATGCCAGCA[A/G]CTGTTTCTGTAGTGA	8925
rs372637180	snp	C/T	0.000331945	0.0128788	intron-variant	HERC1	GRCh38.p7	15:63712724	CAAAGCCTTACATAT[C/T]ATATACCTTGAAAAC	8925
rs372656439	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63745611	GACACTCTCTGCACC[A/C]TACTGCCACTGCTGC	8925
rs372663371	snp	C/T	0.000159987	0.00894249	missense	HERC1	GRCh38.p7	15:63654255	TGCTGAGCTGCCCAT[C/T]GCCGATGCTGTGAGG	8925
rs372678214	snp	C/T	2.1851e-05	0.0033053	synonymous-codon	HERC1	GRCh38.p7	15:63696325	GAGGATCTGATGAAG[C/T]GCCTCTAAACGAAGC	8925
rs372697483	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63751468	TAAGTGACACATCAC[C/T]GTAATACTGTCACTC	8925
rs372699735	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63827730	ATAACAGCTAAGAAG[C/T]AGAAAACCAAATGTA	8925
rs372746021	snp	C/T	0.000180662	0.00950254	synonymous-codon	HERC1	GRCh38.p7	15:63626072	GAGCCTGGCCCGCAC[C/T]GTGTGAATGCTGACT	8925
rs372757884	in-del	-/AACCTTGATGACT			intron-variant	HERC1	GRCh38.p7	15:63637777	GAAAGGGAAGAGTTG[-/AACCTTGATGACT]ATATAACTATGCAGT	8925
rs372761986	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63823022	TTGTACAAATTTAGT[C/T]TGAGATGTCTATTAG	8925
rs372777243	snp	C/T	1.87689e-05	0.00306335	missense	HERC1	GRCh38.p7	15:63696292	GCTACCTTTTTCTTC[C/T]ATCCCAGACAATAGA	8925
rs372779486	snp	A/G	1.66721e-05	0.00288717	intron-variant	HERC1	GRCh38.p7	15:63725535	ACAAAATCATTAGTT[A/G]TTGTGTCTTTATCTG	8925
rs372784541	snp	A/G	1.65701e-05	0.00287833	synonymous-codon	HERC1	GRCh38.p7	15:63758256	CAACTGATGGCTGCT[A/G]TTGCTCCCCCAAACA	8925
rs372792003	snp	C/T	1.79197e-05	0.00299325	synonymous-codon	HERC1	GRCh38.p7	15:63645497	CGTAGCCATCAGTAA[C/T]TGCAACTTGGATCCT	8925
rs372797630	snp	A/G	0.000301539	0.0122751	intron-variant	HERC1	GRCh38.p7	15:63692363	TTATCTTAATAAAAT[A/G]CAAGTAATATCTATA	8925
rs372810110	snp	C/T	7.98818e-05	0.00631938	synonymous-codon	HERC1	GRCh38.p7	15:63746975	GAGCAAATTTCGAAG[C/T]GGACCTGCCTGCCTC	8925
rs372838040	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63666660	ATCCATTTATGTTAT[A/G]CTTTGTAAAGATTTG	8925
rs372848732	snp	A/T	0.000167986	0.00916323	missense	HERC1	GRCh38.p7	15:63643010	GAATCCATACTGTGG[A/T]CTGAATAGCTCCAGA	8925
rs372851744	snp	A/G	1.70554e-05	0.00292017	intron-variant	HERC1	GRCh38.p7	15:63666520	ATATCACTAGATACC[A/G]TGAGTAAAAAGTGTC	8925
rs372856016	snp	C/G	1.65842e-05	0.00287955	missense	HERC1	GRCh38.p7	15:63623731	GGAATATACCTGGCA[C/G]ATCTCTGTGATGGTG	8925
rs372860281	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63619064	AGAGAGGGCATCCCT[C/G]TCTTGTGCCAGTTTT	8925
rs372873653	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63705884	AATAATAAAAAACTA[G/T]CTGAGCATGGTGGTG	8925
rs372881720	snp	A/G	1.65625e-05	0.00287766	missense	HERC1	GRCh38.p7	15:63774921	CTGCCCCAGAATTAG[A/G]AATAGTGACTCCTTT	8925
rs372895414	snp	C/T	8.29194e-05	0.00643839	synonymous-codon	HERC1	GRCh38.p7	15:63677886	TTGGACCTTGGCAGA[C/T]GTGCTGCCCTCTTTG	8925
rs372901527	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63696780	CTGCTACTGCTTTCT[C/T]TATTAATAAGTTTAT	8925
rs372923243	snp	C/G	1.67942e-05	0.00289772	intron-variant	HERC1	GRCh38.p7	15:63628830	GCTGGGAATAAATCA[C/G]AAATATACAGACATT	8925
rs372933242	snp	A/G	1.65611e-05	0.00287755	missense	HERC1	GRCh38.p7	15:63640300	TCATTTGGATTCCAG[A/G]ATGCAGGGTCAGGGA	8925
rs372965540	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63681475	GTGTTGGGATTATAG[A/G]CATCAGCCACTACAC	8925
rs372967185	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63617152	TCTCCTAATGCTATC[A/C]CTCCCCGCTCCCCTC	8925
rs372970354	snp	A/G	0.000392934	0.0140112	intron-variant	HERC1	GRCh38.p7	15:63630678	GAAATGTTATGCACC[A/G]CACAACACAGTGCTT	8925
rs373029122	snp	C/T	3.17475e-05	0.00398406	intron-variant	HERC1	GRCh38.p7	15:63648209	CAGACACTAACATGA[C/T]CAAAACAAAAGAGTA	8925
rs373031004	snp	A/G	2.67483e-05	0.00365697	missense	HERC1	GRCh38.p7	15:63622857	GTGGCATTGGGAGAG[A/G]GTATAAGAAGGTCAA	8925
rs373063842	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63640792	GGATCCAATCTAAGC[G/T]ATCACACTGCATATA	8925
rs373067186	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63730783	GAGAGAGAACAAATT[A/T]GGCTGAAGAGCACAG	8925
rs373069539	snp	A/C/G/T	0.000282841	0.0118894	intron-variant	HERC1	GRCh38.p7	15:63713320	ATAAAGGGAAGTGAG[A/C/G/T]AGGTCATGTTTTCAG	8925
rs373071533	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63704186	GTCAAAGGGCAGTCA[C/G]TAAATATACAATATT	8925
rs373074601	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63742043	GCAAGAATTTTGATA[A/G]TGATTGCACTCAATC	8925
rs373075664	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63754444	ATATATAACTGAAAA[A/C]TAAATTTTTAAAAAA	8925
rs373088219	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63722492	GTTTCAGTTACTTGC[A/G]ATCAACTGTGGTCCA	8925
rs373088516	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63783228	CATTCATGAAAGGAG[A/G]AGCCAATCAATGCAG	8925
rs373088843	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63773112	TAACTAAATAGATTT[A/G]TTGGTTGACATCTGG	8925
rs373098342	snp	A/C/T	6.53721e-05	0.00571686	missense	HERC1	GRCh38.p7	15:63652472	TGGTAACATTCCATA[A/C/T]GCGGATGGTGCCATC	8925
rs373100664	snp	C/T	1.65603e-05	0.00287747	missense	HERC1	GRCh38.p7	15:63636014	TGGGCCGCCGCTGCC[C/T]GTCGCTGTTCCCATG	8925
rs373101455	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63693208	AACCCAGAAAACAAA[C/G]AGATATCAAAACCCT	8925
rs373104999	snp	C/T	3.99265e-05	0.00446785	synonymous-codon	HERC1	GRCh38.p7	15:63729243	AAACTCACCTCTTAA[C/T]TTTTCTCCAACACTG	8925
rs373105634	snp	C/G	1.65864e-05	0.00287974	missense	HERC1	GRCh38.p7	15:63658636	TAAAGCCACCACACG[C/G]TCATGAGGGTTTGCT	8925
rs373110616	snp	C/G	7.90045e-05	0.00628459	missense	HERC1	GRCh38.p7	15:63693996	TCAGTTTCTCCACTG[C/G]AGTCAACTTTTTTTT	8925
rs373111139	snp	A/G	1.65688e-05	0.00287821	missense	HERC1	GRCh38.p7	15:63666024	CCACTGCCTAGAACG[A/G]CTGCTCCAGGCCTAG	8925
rs373117024	snp	G/T	1.69963e-05	0.00291511	missense	HERC1	GRCh38.p7	15:63698775	TGATGGAGGCCTGGG[G/T]ACTTGTAGACATACT	8925
rs373121321	in-del	-/CCCGCT	0.0142736	0.0832652	intron-variant	HERC1	GRCh38.p7	15:63617155	CTAATGCTATCCCTC[-/CCCGCT]CCCGCTCCCCTCACC	8925
rs373126369	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63811843	ACAGAAAGGAAAAAA[A/C]AAAGGTTATCTTTGA	8925
rs373131810	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63756266	ATATAAGAATTAAAA[A/T]TCAATAATGTATACA	8925
rs373135635	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63665492	GTGAGCCGATATCGC[A/G]CCACTGCACTCCAGC	8925
rs373136951	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63626890	TAAGAGCTTTACATG[A/C]ATGGGGCCACTTACT	8925
rs373138757	in-del	-/AAC	0.000284774	0.0119292	intron-variant	HERC1	GRCh38.p7	15:63633981	GCCACCTAAAGAAAT[-/AAC]AGCATTCCGTAAGGC	8925
rs373139298	in-del	-/CAAAA	0.17654	0.238964	intron-variant	HERC1	GRCh38.p7	15:63649351	AGCGAGACTCCTTCT[-/CAAAA]CAAAACAAAACAAAA	8925
rs373140770	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63692166	TTAGGTTTGTAATCT[C/G]AACAAAGAGGATGAA	8925
rs373149343	snp	C/T	1.65762e-05	0.00287886	missense	HERC1	GRCh38.p7	15:63727770	GCCGAGCCACTGACA[C/T]AGGGAGTAACAGCAG	8925
rs373160324	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63738845	CCTTATTTTATTCTA[G/T]TACTTTTACCCTTTT	8925
rs373161086	in-del	-/TTTA			intron-variant	HERC1	GRCh38.p7	15:63739916	CTTAGCATATTTTAT[-/TTTA]TTTTTTTTTTTTCAG	8925
rs373166035	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63787157	TCAATAAATTATTAT[C/T]ATCATATTATTATTT	8925
rs373180491	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63804443	TACAAAAAATTAGCC[A/G]GGCATGGTGGCGGGC	8925
rs373198279	snp	A/G	0.00038117	0.0138	intron-variant	HERC1	GRCh38.p7	15:63694727	GTACCATAACCTCGG[A/G]CTAAAATGTAACCTG	8925
rs373201199	snp	C/T	1.77118e-05	0.00297583	missense	HERC1	GRCh38.p7	15:63656206	GCCTTGCTATGCCCA[C/T]CTCGTGATCGTTCTG	8925
rs373201379	snp	A/G	0.000127073	0.00796996	intron-variant	HERC1	GRCh38.p7	15:63675167	AAGTGAGGGAAAGAC[A/G]GGAGGAAGGTACGGA	8925
rs373204239	snp	A/G			upstream-variant-2KB	HERC1	GRCh38.p7	15:63835471	GTTGATGTCATCTAC[A/G]TCACTCACAAATATG	8925
rs373219506	snp	A/G	0.00013157	0.00810974	intron-variant	HERC1	GRCh38.p7	15:63723373	AAAAAAAATACTCAC[A/G]TTACCAATTTTAACA	8925
rs373223059	snp	A/G	0.00018729	0.00967522	intron-variant	HERC1	GRCh38.p7	15:63755335	AACTACCTGCATTGC[A/G]CACAAGTAAATACGA	8925
rs373226973	snp	C/T	3.31274e-05	0.00406972	missense	HERC1	GRCh38.p7	15:63774986	CCCATAGGAGGAATC[C/T]TGCTTTCATTTGCTA	8925
rs373231410	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63821102	GCATTGTTTAACTGA[C/G]TCAACAGTCCTCCTT	8925
rs373254747	snp	C/T	0.000167986	0.00916323	intron-variant	HERC1	GRCh38.p7	15:63756399	ATTACAACTCCAATG[C/T]ATCTAATTATTTTTA	8925
rs373270295	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63796932	GTCTTGTTCTATCAG[C/T]AATTCCAAAAGAGAG	8925
rs373281172	snp	C/T	0.000152742	0.00873771	missense	HERC1	GRCh38.p7	15:63637573	CCTAATCTGCCATAA[C/T]TTCCTTCCCCACAAG	8925
rs373301641	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63806119	CATCATCACTACAGA[G/T]ACCTCCCAAATCACC	8925
rs373325927	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63677493	AGATTAGCTGGCTGG[C/T]TTTTTACTATGCCAG	8925
rs373342297	snp	A/G	2.25106e-05	0.00335482	intron-variant	HERC1	GRCh38.p7	15:63643066	GAGCCATCCTAAAAT[A/G]AGATATATTTACCAA	8925
rs373343492	snp	A/G			synonymous-codon	HERC1	GRCh38.p7	15:63698959	TTTCAGGCGAGCCCA[A/G]GAGTCACTCAGGGAT	8925
rs373354422	in-del	-/ATATATATAC			intron-variant	HERC1	GRCh38.p7	15:63829492	TAAATATATATATAT[-/ATATATATAC]ACACACACACATATA	8925
rs373368217	snp	C/G/T	3.44669e-05	0.0041512	intron-variant	HERC1	GRCh38.p7	15:63658743	ATAATTCTGTTTTGT[C/G/T]CTCAACAAGGTAAGA	8925
rs373375539	snp	A/G	0.000165986	0.00910854	intron-variant	HERC1	GRCh38.p7	15:63694283	GACCAGACTTCATAC[A/G]GTTCTACAAAGACAT	8925
rs373384499	snp	A/G	0.000346081	0.0131499	synonymous-codon	HERC1	GRCh38.p7	15:63718580	AAACTTTACCCATCT[A/G]TCCCGTGATGATGAC	8925
rs373392060	snp	A/G	0.000149082	0.00863242	synonymous-codon	HERC1	GRCh38.p7	15:63694778	CGTTTACTTACCAAT[A/G]TGATGCTTGTTTGCT	8925
rs373393506	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63798315	AATGACTACTCAGTG[A/C]TTAACCAGTTAAAGA	8925
rs373399705	in-del	-/A			frameshift-variant	HERC1	GRCh38.p7	15:63733035	AGATTTCCGTAGCCA[-/A]GTACACACAGAAGAT	8925
rs373401846	snp	C/T	0.000155222	0.00880834	intron-variant	HERC1	GRCh38.p7	15:63755348	GCACACAAGTAAATA[C/T]GATGAGTATGCACAT	8925
rs373423213	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63609451	CCGTGGCCCTCGAGG[A/C]TCTGGGTGAAGATGT	8925
rs373424376	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63625564	CCAGGCATGGTGGCC[C/G]AGGCCTGTAATCTCA	8925
rs373436675	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63829571	TGTGTGTATATATAT[A/G]TATATATATATATAT	8925
rs373441556	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63742935	TTAATAGCTGGTCTA[C/T]AGTTTTTCTTTTCTT	8925
rs373447462	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63816116	AACATTTCCCAAAAC[C/T]TGTTCCTCAGATCAC	8925
rs373450046	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63765094	GTTCCGAAGCAGATA[A/G]CTACAGATGAAAGGG	8925
rs373455045	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63681203	GTTTTGTTTTGTTTT[G/T]TTTTTAATTTTCTAA	8925
rs373459995	snp	C/T	0.000430877	0.0146715	synonymous-codon	HERC1	GRCh38.p7	15:63680582	GGCTTCCATGTCTAA[C/T]ACACAGGTAATGAAA	8925
rs373470800	snp	A/G	0.000233497	0.0108025	synonymous-codon	HERC1	GRCh38.p7	15:63775372	CAATGCTAGCTGGCT[A/G]CTAAGAAGGGCATCC	8925
rs373488853	snp	A/G	0.000159987	0.00894248	synonymous-codon	HERC1	GRCh38.p7	15:63612307	CAGTGTTGGCTGGTA[A/G]TCGAGATCTTCCTGA	8925
rs373489534	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63829890	AAATAAATAATGATA[C/G]TATTGGATTATAATC	8925
rs373493156	snp	C/G	1.86079e-05	0.00305018	missense	HERC1	GRCh38.p7	15:63729335	GCAACAAAAGCTGAA[C/G]ATGTTTATGAAGCAA	8925
rs373494715	snp	C/G	1.66843e-05	0.00288823	missense	HERC1	GRCh38.p7	15:63698800	CATACTTTCCTCTGG[C/G]TCTTTAAAACCTGGG	8925
rs373502276	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63613099	TGGGAAGTCCTTCTT[C/T]AGGAAGGCAATAGAA	8925
rs373506688	snp	C/T	2.33664e-05	0.00341799	synonymous-codon	HERC1	GRCh38.p7	15:63764162	TGTTCTGGTTGGTTC[C/T]CTCCACTGACTCCGA	8925
rs373536971	snp	C/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63621658	TGGTCTTTTCACATA[C/G]TCCCATATTTCTTGG	8925
rs373538130	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63672144	AAAATTATTTTCATG[C/G]AGGTGAATATTCCAA	8925
rs373553963	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63776326	CACCCCACCCAAACC[A/T]GTCCCTCCTGTAGAC	8925
rs373557592	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63653491	GTTACAGCTCAGAGA[C/T]CCCATGGGTTAGATT	8925
rs373567163	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63692801	TATGCTATAACTATG[A/C]TGACTAAGTATAATA	8925
rs373579120	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63763549	AAATGGAGGAGGGAA[C/T]CTAGAGATTAAAATA	8925
rs373585182	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63738994	TTATTTTTTTTTTTT[A/C]AAATTGACATATAAT	8925
rs373586204	snp	C/T	0.000128023	0.00799969	intron-variant	HERC1	GRCh38.p7	15:63645445	CAGTCTATACCAATA[C/T]AAAAACTAAGACGTA	8925
rs373587510	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63742617	ACTTTTTCATAGATG[A/C]CCTTTTCAGGTTAAG	8925
rs373601092	snp	A/G	0.000160506	0.00895696	intron-variant	HERC1	GRCh38.p7	15:63764220	ATTGCGGGACACAGC[A/G]TAGGAAGGGGAGAGA	8925
rs373601975	snp	A/C	1.88535e-05	0.00307024	missense	HERC1	GRCh38.p7	15:63696143	TAGTGATGCAATCGG[A/C]CACTCTCTCCCTTGC	8925
rs373605815	snp	A/G	0.000161987	0.00899818	missense	HERC1	GRCh38.p7	15:63725421	ACCGCCCAATAAGGA[A/G]AGCAATTGTTCTTTC	8925
rs373607540	snp	C/T	1.65883e-05	0.00287991	missense	HERC1	GRCh38.p7	15:63756556	CTTCTGTCGTAAAGG[C/T]TAAAGTGTGACCATC	8925
rs373607585	in-del	-/C	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63758865	CCATCTAGTAAAAAA[-/C]ATCACAATGTACTCA	8925
rs373613620	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63829582	TATATATATATATAT[-/A]ATATATATATATAAT	8925
rs373625041	snp	G/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63671686	GAGCTTTAAAAAGTT[G/T]CCCAGGTGGCCTTGG	8925
rs373636527	snp	A/G	0.0174175	0.0916809	intron-variant	HERC1	GRCh38.p7	15:63646681	GGAGTGGTGGCGGGC[A/G]CCTGTAATCCCAGCT	8925
rs373656484	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63690186	AAAAAAAAAAAAAAA[A/G]AAATATTAACCTATT	8925
rs373656985	snp	G/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63701032	GTTTTTTGGGGGGGT[G/T]TTTTTTTTTAAATAT	8925
rs373657295	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63743257	TTTTTTTCTTTTTTT[C/T]TTTTTCTTTTTTTTT	8925
rs373680532	snp	C/T	1.65872e-05	0.00287981	synonymous-codon	HERC1	GRCh38.p7	15:63640167	CATTAGAAATACAAG[C/T]TCATCCTCTGGAACA	8925
rs373686089	snp	C/T	8.28027e-05	0.00643386	synonymous-codon	HERC1	GRCh38.p7	15:63663125	ATTAAAGTCATACAA[C/T]GCCCCTGGGTCTTGC	8925
rs373699871	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63619910	ATTAGTCTTGCTAGC[A/G]GTCTATCAATTTTGT	8925
rs373716359	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63690166	GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA	8925
rs373727879	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63661291	AATTCTATTCCATAA[A/T]GCCTTAAAGATTTTA	8925
rs373733355	in-del	-/C			intron-variant	HERC1	GRCh38.p7	15:63805947	GACCCTATCTCAAAA[-/C]AAAAAAAAAAAAACA	8925
rs373742193	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63738462	TTATATAATGGTTAT[C/G]TAAGACATTAACATA	8925
rs373751059	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63768871	AACATGCTTAGCACA[A/G]TTCCCACTACATAGT	8925
rs373763022	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63793280	GGTCGTAAAGACCAC[A/G]CTGATAAAACTGGTT	8925
rs373764252	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63673253	AATCCTACAAATAAA[A/C]ATAACTAAAATATGA	8925
rs373780037	snp	C/T	1.71425e-05	0.00292762	missense	HERC1	GRCh38.p7	15:63666121	TGGCAAGGACAGTGA[C/T]ATTCTGGGCATCAGC	8925
rs373783943	snp	A/G	0.00228586	0.0337299	synonymous-codon	HERC1	GRCh38.p7	15:63698941	TAACCAGTCTCTGCT[A/G]TGTTTCAGGCGAGCC	8925
rs373816223	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63786540	ATAAACAAAATGTCA[C/T]ATTATCTACACAGTG	8925
rs373824145	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63755791	AACAAAAAAAGAAAG[A/G]AAGAAAAGAGAGGAA	8925
rs373831351	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63825838	GTGGGTCTCAGCTCA[C/T]TGCAACCTCCACCTC	8925
rs373840931	in-del	-/A/AA/AAA			intron-variant	HERC1	GRCh38.p7	15:63808124	GTAATTCTAGTTGAC[-/A/AA/AAA]AAAAAAAAAAAAATA	8925
rs373843941	snp	A/C	1.66299e-05	0.00288352	missense	HERC1	GRCh38.p7	15:63694483	GAAATTGCCAAAGAA[A/C]CATCTACTGGTTGAT	8925
rs373847833	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63773700	AGGTGCGCACCACCA[C/T]ACCCGGATAATTTTT	8925
rs373860230	snp	C/T	1.66228e-05	0.0028829	intron-variant	HERC1	GRCh38.p7	15:63752940	TCTAAGTCTTTTATA[C/T]TCATCCCTTAGTCCT	8925
rs373866588	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63793396	AATTATAATGCATTA[A/G]TATGCTAAAACACAC	8925
rs373874680	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63618772	AGCAACTGTGAATGG[A/G]AGTTCACTCATGATT	8925
rs373882525	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63829461	GTGTGTGTGTGTGTG[C/T]ACATATATGTTTATA	8925
rs373886897	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63683338	CAAAACAAGTGTCTA[C/T]AACTGGTGGGTTTTT	8925
rs373893519	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63717911	TCAATCTTCATTTCC[A/C]ATGGTAGACAACTCT	8925
rs373898861	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63765835	AGGCTGTCACAGGCA[C/T]GTCCTTAACCTTGGC	8925
rs373907100	snp	A/T	0.000163987	0.00905352	missense	HERC1	GRCh38.p7	15:63725495	GGCAGACCAGCAGGA[A/T]CAATTAGTTCTGGCC	8925
rs373909610	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63644028	AGTGACATAGGTAAG[G/T]CCTGTCTATAGGGCT	8925
rs373921368	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63636940	AATGAAAAGAACCTG[A/T]GCTTCTAGGAACTTG	8925
rs373964013	in-del	-/C	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63664075	CTAACAACCACAGAG[-/C]AGTACATCAGAAAAG	8925
rs374003523	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63744138	TGTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT	8925
rs374019165	snp	C/T	3.52212e-05	0.00419635	missense	HERC1	GRCh38.p7	15:63634809	TTTCCAAGACCCAGA[C/T]GACCATAGTCACCAT	8925
rs374025274	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63717076	CAGTCATAAATACCA[C/T]TCAGTATAAAGCACA	8925
rs374033845	snp	A/G	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63748080	AAAACATAAAAATTA[A/G]TCGGGCATGGTGGTA	8925
rs374038284	snp	A/C/T	5.06721e-05	0.00503328	intron-variant	HERC1	GRCh38.p7	15:63651220	TTTAAAAAACTACTT[A/C/T]CAGCAGTTTACTAGT	8925
rs374040576	snp	C/T	1.65787e-05	0.00287907	synonymous-codon	HERC1	GRCh38.p7	15:63678099	CTCTTTGCTCTCCTT[C/T]TCCTCTCTCATTTCA	8925
rs374048295	snp	A/G	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63739753	CGAGGCAGGATAATC[A/G]CTTGAACCCAGGACG	8925
rs374050295	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63663777	TCATATAGAAAAAAA[-/A]CTTCAATAAATATTG	8925
rs374064734	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63808108	TTTAGCATAACATTA[C/T]AGTAATTCTAGTTGA	8925
rs374074455	in-del	-/ATT	0.00597247	0.0543191	intron-variant	HERC1	GRCh38.p7	15:63613009	TGTCTTTTGAAAATA[-/ATT]ATATCCTTTTTGTAA	8925
rs374085693	in-del	-/C	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63818100	AATTACTCTTATTTG[-/C]CAAGTCTGTTAACAA	8925
rs374133987	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63783740	CCTTTGAGAATCTGA[C/T]AAAAGCAGTAGACCG	8925
rs374141345	snp	A/G/T	3.34729e-05	0.00409091	missense	HERC1	GRCh38.p7	15:63694387	AGCTGGGAAACACCC[A/G/T]TCTTTGGCAACAACT	8925
rs374144725	snp	G/T	1.65781e-05	0.00287902	synonymous-codon	HERC1	GRCh38.p7	15:63749486	AGGACCTGTGGAATT[G/T]CCCTGACCACATTGC	8925
rs374151135	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63650124	TTAAAGTTTTTCAGC[C/T]GGGCACAGTGGCTCA	8925
rs374152989	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63695849	CCTCCCAAACTCCAA[C/T]CCCTATCCTTACTTG	8925
rs374154519	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63613405	TCCTCCAATATTATA[C/T]AGTAGTGCATACCCT	8925
rs374157240	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63665826	ATTTATCAACTTTAC[A/T]TACAATTAGAAGCAT	8925
rs374160412	snp	A/C	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63632009	AACCTACATCTTCAT[A/C]ATCAATCCTTCTGGA	8925
rs374170554	snp	C/G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63721732	GACAGGATAAGAGAA[C/G/T]GACACAGAGAAAGAA	8925
rs374174261	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63746131	GTTAAATTACTGATT[C/T]GATATATATTTTTTT	8925
rs374223563	snp	A/C	0.000740762	0.019231	intron-variant	HERC1	GRCh38.p7	15:63643571	ATTCATTATTTTTAA[A/C]ATGCATTAAAATAAA	8925
rs374224646	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63638336	TGGACAAGCTTTATC[A/C]CACAATAAGACAAGC	8925
rs374234775	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63743524	CACCTTGGCCTCCAA[A/C]AGTGCTGGGATTACA	8925
rs374244666	snp	C/T	8.08048e-05	0.00635578	missense	HERC1	GRCh38.p7	15:63637595	CCCCACAAGCCAACA[C/T]TGTGCCATTGGCCTG	8925
rs374249242	snp	C/T	5.21173e-05	0.0051045	missense, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609181	ATGGCATAGCGCAGG[C/T]GCTCGGCCATGACCA	8925
rs374255542	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63679343	TTGACATTAAAAATA[C/T]GTATTTTTAAAAACA	8925
rs374261680	snp	A/G	6.7555e-05	0.00581145	synonymous-codon	HERC1	GRCh38.p7	15:63659866	TAAACCAAGCGGTCC[A/G]GCAAGTAATTCAAAT	8925
rs374266047	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63774249	TACTAGGCTGTTAGC[G/T]CCATGGGGGTGGAAA	8925
rs374269292	snp	A/G/T	0.000149239	0.00863706	missense	HERC1	GRCh38.p7	15:63616467	ATCCCACTGTCTTCA[A/G/T]TGTGAAGAATGCTGT	8925
rs374272319	in-del	-/G			intron-variant	HERC1	GRCh38.p7	15:63683155	AAAAAAAAAAAAAAA[-/G]AAAGAAAAAAAATTA	8925
rs374275205	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63761586	GAGCAAGACTGTCTC[-/A]AAAAAAAAAAAAAAA	8925
rs374308387	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63642438	TGCCTCCTGGGTTCA[A/C]CCAATTCTCCCGCCT	8925
rs374330014	in-del	-/CCC			intron-variant	HERC1	GRCh38.p7	15:63720101	CAGGTGCTTTTTCTT[-/CCC]TTTTTTTTTTTTTTT	8925
rs374357040	snp	C/T	1.65916e-05	0.00288019	intron-variant	HERC1	GRCh38.p7	15:63644946	GACTCTGATGTCATA[C/T]ACTTTCCATAGTTTC	8925
rs374357693	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63806631	AAGGGCTCAGAACAT[C/T]GTAGAAGAGGAATTA	8925
rs374359281	snp	C/T	0.000396368	0.0140722	intron-variant	HERC1	GRCh38.p7	15:63615760	CCTCCCGAGATGTTT[C/T]ATCTCACCTGTCTGT	8925
rs374359585	snp	C/G	7.00611e-05	0.00591825	missense	HERC1	GRCh38.p7	15:63649797	CTTCAATCAGTCCCA[C/G]AGATCCATCCATCCG	8925
rs374360804	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63799036	TTACTTTTTAAGATA[C/T]GTTTCAGAACTAGGT	8925
rs374367917	snp	C/T	1.65649e-05	0.00287788	missense	HERC1	GRCh38.p7	15:63677950	TGCTTGTGAACACAC[C/T]GACCTCCAACTCTAA	8925
rs374369254	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63654006	TGTGTATGTGTACGT[A/G]TGAAAGAGAGTGACA	8925
rs374374721	snp	A/G	2.08153e-05	0.00322602	intron-variant	HERC1	GRCh38.p7	15:63694909	CCTGAATTACACATA[A/G]AGAATTACTTTTTCT	8925
rs374379859	snp	G/T	0.000159987	0.00894248	missense	HERC1	GRCh38.p7	15:63672665	GTGCCTGCTGGGCAG[G/T]GTCACTTTCTTCAGC	8925
rs374385019	snp	A/G	8.32466e-05	0.00645108	synonymous-codon	HERC1	GRCh38.p7	15:63725320	GTCCATTTCTACACC[A/G]TCACTGAACAGTGGC	8925
rs374394141	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63723042	AGGGAAAAACAAATT[C/G]TTTAAAAATGTTAAT	8925
rs374400992	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63678980	TATGCACATAAAGTG[C/T]TTATTAGTACATTGC	8925
rs374417941	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63769362	GAGGCGGGAGCTGCA[A/G]TGAGACGAGATCTTG	8925
rs374444954	snp	A/C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63812811	AAAAAATTATTAAGG[A/C/T]AAGAAATCAAAGATA	8925
rs374448372	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63770916	GTTCTAGGCTGGGCA[C/T]GGTGGCTCACGCCTG	8925
rs374477507	snp	C/G	3.35458e-05	0.00409534	intron-variant	HERC1	GRCh38.p7	15:63640140	AATAATAGCAGCTCA[C/G]AGTACATTTACCATT	8925
rs374478029	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63614723	TCAAAAGAACCATTT[C/T]TGGACACCATATTTA	8925
rs374495794	snp	C/T	3.39795e-05	0.00412172	missense	HERC1	GRCh38.p7	15:63674659	GCACCGAGGTAAAGA[C/T]AGGACAGCTGGACTG	8925
rs374526048	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63726434	GATAAGTTATCTAAA[A/G]GGAAAATGGATAAAT	8925
rs374531552	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63764850	GCAACTTGCTAATAA[G/T]ATCTCAGGAGCTGGG	8925
rs374543092	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63754930	TGCTCATGTTGACTT[C/G]TTTTCATTACCCACT	8925
rs374552441	snp	C/G	0.000167986	0.00916322	intron-variant	HERC1	GRCh38.p7	15:63638388	TCCCATGTTTCTTTT[C/G]TATTTTTTATCCTGT	8925
rs374565654	snp	A/G	0.000130472	0.00807582	missense	HERC1	GRCh38.p7	15:63645591	CAGCACCAGCATCCC[A/G]AAATAGAGCCCCAGA	8925
rs374567563	snp	A/G/T	4.97668e-05	0.00498812	synonymous-codon	HERC1	GRCh38.p7	15:63674799	TAAAGAAAATGAAGC[A/G/T]ATTTCATTTTCTGAT	8925
rs374567906	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63759079	TTATTTGTTATATAG[C/G]CCATTTTTAAGGATA	8925
rs374571339	snp	C/T	0.000760127	0.0194804	intron-variant	HERC1	GRCh38.p7	15:63659945	CAGTCTTCTGGAATT[C/T]AAATAAATAAATGTA	8925
rs374580110	snp	A/G	9.98104e-05	0.00706365	synonymous-codon	HERC1	GRCh38.p7	15:63694452	CAACTGTGACAATAC[A/G]TTTAGCAGACCAGTG	8925
rs374582826	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63824568	AAAAGAAAACCACCA[C/T]ATGATCCAGCAATCT	8925
rs374630578	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63704824	GCTCACTGCAAGCTC[C/T]GCTTCCTGGGTTCAC	8925
rs374631238	snp	G/T	0.00325292	0.040198	intron-variant	HERC1	GRCh38.p7	15:63652550	TCATTACCTAGAAAA[G/T]TTGAAACAGGTAGTC	8925
rs374648046	snp	A/G	1.662e-05	0.00288266	missense	HERC1	GRCh38.p7	15:63674378	ACTGGTCTTCCAAAA[A/G]CCCATGAACCACTAA	8925
rs374650888	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63785387	TGCACCACTGCACTC[C/G]AGCCTGGGCAATAAG	8925
rs374657243	snp	A/G	0.000167986	0.00916322	missense	HERC1	GRCh38.p7	15:63692428	GAAGAACATTTCTGA[A/G]ATGCTATATTTAGAA	8925
rs374671127	snp	C/T	0.000167986	0.00916322	synonymous-codon	HERC1	GRCh38.p7	15:63718631	GTTCTTGCAAGCAAG[C/T]AAACGACTTCGAACT	8925
rs374688915	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63616249	TAAGTGCAGGAGCCT[G/T]CTCTATTAGAAGCTG	8925
rs374706985	snp	C/T	1.74775e-05	0.00295608	intron-variant	HERC1	GRCh38.p7	15:63626171	TGTCCAGAAAGCAAA[C/T]GGGCACTTATGAAGG	8925
rs374710929	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63670981	CTAAGGTGGGCAGAT[C/T]CCCTGAGGTTGGGAG	8925
rs374711611	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63824005	AAATGACTTGAATAG[A/G]TATTTCTCCAAATAG	8925
rs374714129	in-del	-/TATATAAATATA			intron-variant	HERC1	GRCh38.p7	15:63829473	GTGCACATATATGTT[-/TATATAAATATA]TATATATATATATAT	8925
rs374722551	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63813866	TGAGGTCAGGAGTTT[A/G]AGACCAGCCTGGTGA	8925
rs374732664	snp	A/G	0.000200669	0.0100147	intron-variant	HERC1	GRCh38.p7	15:63635927	AACTAGTATATTTAC[A/G]ATGAAAGGCAAACTT	8925
rs374739089	snp	C/T	6.37925e-05	0.00564731	missense	HERC1	GRCh38.p7	15:63615850	GTGAGTGGGATACTA[C/T]TTCCACCAGGGATTA	8925
rs374778145	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63689146	AGATCCGGGAGAAAG[C/T]GTTTTGAAAATAACA	8925
rs374783494	snp	A/G	0.000182157	0.00954176	synonymous-codon	HERC1	GRCh38.p7	15:63640308	ATTCCAGGATGCAGG[A/G]TCAGGGAGACAGTTC	8925
rs374791507	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63707801	GGGTGTGGTAGCACA[C/T]GCCTGTAATCCCAGC	8925
rs374794725	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63687597	TCAATGTGCATTTAT[C/T]AAGCATCTCTATTCT	8925
rs374799571	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63734623	TAACCCATCAAGTAC[G/T]TATGCTCCAAGAACA	8925
rs374805772	snp	C/T	0.000190937	0.00976894	intron-variant	HERC1	GRCh38.p7	15:63630659	AACAAAACAAAAACA[C/T]GTGGAAATGTTATGC	8925
rs374818851	snp	A/G	9.16128e-05	0.00676742	intron-variant	HERC1	GRCh38.p7	15:63655718	CGATTAGAAGACTGT[A/G]TGTTTCAGTAGTATG	8925
rs374823124	snp	C/T	1.68074e-05	0.00289887	intron-variant	HERC1	GRCh38.p7	15:63634012	GCAAATCACAAGACC[C/T]AAAACACACTCCCCC	8925
rs374828607	snp	C/G/T	3.32509e-05	0.00407732	intron-variant	HERC1	GRCh38.p7	15:63666477	GTCTGACAAGGCTGA[C/G/T]ACAAAAGGAAGAGAA	8925
rs374833444	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63632286	TGAATGCCTGGGTTA[C/T]GAACCTACTCAAGAT	8925
rs374839239	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63629434	AGTAATAACAGAATG[A/G]TCTATGGAGCTTTTA	8925
rs374843960	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63650598	GTCTGTAACTATTAA[A/T]AGGGCAAAATGGTAG	8925
rs374847616	in-del	-/AAAA			intron-variant	HERC1	GRCh38.p7	15:63811809	TGAGACTCCGTCTCC[-/AAAA]AAAAAAAAAAAAAAA	8925
rs374850195	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63614027	TGAGGTATGGGGCTG[C/G]CTGCTTGGAGATGGC	8925
rs374864238	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63788874	AGCAAGACTCCGTCT[A/C]AAAAAAAAAAAAAAA	8925
rs374871616	in-del	-/A	0.32955	0.237006	intron-variant	HERC1	GRCh38.p7	15:63730158	TTTGTTTTTTCCATT[-/A]AAAAAAAAAAAAGCA	8925
rs374885302	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63612048	AAAAAATTAGCCAGG[C/T]GTGGTGGCACGCACC	8925
rs374892433	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63634525	AATAAGGGTTACATT[G/T]GTTGGTTTGTCACAT	8925
rs374893320	snp	A/G/T			intron-variant	HERC1	GRCh38.p7	15:63610712	CAGCACAGGGAGGAA[A/G/T]AGCTTTGGCTACACC	8925
rs374895346	snp	A/T	0.0566069	0.158427	intron-variant	HERC1	GRCh38.p7	15:63829592	ATATATATATATATA[A/T]ATAATATACTGATAT	8925
rs374898558	snp	A/G	7.20955e-05	0.00600354	intron-variant	HERC1	GRCh38.p7	15:63692609	CAACCAAGAGCCAAC[A/G]AGAAATAGTCTTATA	8925
rs374904548	snp	A/G	4.96915e-05	0.0049843	missense	HERC1	GRCh38.p7	15:63716350	CCTCTTCATCCTCTG[A/G]CTCCGGATGCCCCTC	8925
rs374912485	snp	C/T	0.000161987	0.00899818	synonymous-codon	HERC1	GRCh38.p7	15:63775237	CGGAGAATGCTGCTG[C/T]TGCTTCACCTTGCCT	8925
rs374945183	snp	A/G	0.000107293	0.0073236	synonymous-codon	HERC1	GRCh38.p7	15:63641571	CACCCTGCTGTTTCA[A/G]TGCTGTCCTACAGGT	8925
rs374953824	snp	C/G	0.00222495	0.0332795	intron-variant	HERC1	GRCh38.p7	15:63628819	GCCTAAGCCGAGCTG[C/G]GAATAAATCACAAAT	8925
rs374956133	in-del	-/GTTTTGTTTTGTTTT			intron-variant	HERC1	GRCh38.p7	15:63681193	GTTTTGTTTTGTTTT[-/GTTTTGTTTTGTTTT]TAATTTTCTAAAGAG	8925
rs374960481	snp	A/G	1.65655e-05	0.00287793	synonymous-codon	HERC1	GRCh38.p7	15:63654146	AGCCTCCAATTTGAT[A/G]AAGGAGCATTTTCTA	8925
rs374963715	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63798547	TATCTTCAAACTTTA[A/C]AAAAAAAAAAAAAAA	8925
rs374995336	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63762124	TGGGGGCAACAAATG[C/T]GTAAGATCAGCCAGA	8925
rs375000040	in-del	-/TT			intron-variant	HERC1	GRCh38.p7	15:63728939	TTTTTTTTTTTTTTT[-/TT]AAAACCTGCtctttc	8925
rs375001242	snp	A/G	0.000296311	0.0121683	missense	HERC1	GRCh38.p7	15:63718605	GATGACCTTGTTTGA[A/G]TAAGTTCAAGGTTCT	8925
rs375001966	snp	C/T	0.000356068	0.0133382	intron-variant	HERC1	GRCh38.p7	15:63658502	CCAGCTAATGTACAC[C/T]AGAAGTTAACTTAGC	8925
rs375002833	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63676482	ATTGTTCCGGCCGAG[C/T]GTGGTGGCTCATGTC	8925
rs375010040	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63731740	AGGAAACAATATTAA[C/T]TGATACACAAACAAT	8925
rs375013051	in-del	-/AGTACTACCATGAAT			intron-variant	HERC1	GRCh38.p7	15:63656995	AGTACTACCATGAAT[-/AGTACTACCATGAAT]GATTGGTCTTTAGGG	8925
rs375052098	snp	A/G/T			intron-variant	HERC1	GRCh38.p7	15:63623531	TATTTATGTAGTAAG[A/G/T]TATCTTGACAAAGCG	8925
rs375057750	in-del	-/GACAAAACAAAAC			intron-variant	HERC1	GRCh38.p7	15:63787983	AAAAAAAAAAAAAAA[-/GACAAAACAAAAC]AAAAAACCTTACAAG	8925
rs375066388	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63794713	TAGCAGGAGATGCCA[C/T]TCTTTCATCTTAGAA	8925
rs375073960	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63612645	GGCGCCTCCTGATGC[C/T]TGCTCGTCCGCTCCC	8925
rs375083552	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63639563	CTTAATTTATATTTG[C/T]CTGTTTCATATTGTA	8925
rs375083953	snp	C/G	0.000225428	0.0106143	missense	HERC1	GRCh38.p7	15:63655802	CCCCTTTGTCTGCTA[C/G]CAATGCCACAAGGGC	8925
rs375085351	in-del	-/AGTCAGGAGGTTGAGAC			intron-variant	HERC1	GRCh38.p7	15:63729809	AGGTACATCACCTGA[-/AGTCAGGAGGTTGAGAC]CAGCCTGGCCAACAT	8925
rs375092246	snp	A/G	1.70313e-05	0.00291811	missense	HERC1	GRCh38.p7	15:63712861	AATTTGGGCTTGTGT[A/G]GACTAGCCGGCTCTC	8925
rs375092681	snp	A/G	1.71773e-05	0.00293059	intron-variant	HERC1	GRCh38.p7	15:63686578	TTTGGAATAATCCAT[A/G]TCTCAGATAAGATAT	8925
rs375095850	snp	A/G	6.90596e-05	0.0058758	missense	HERC1	GRCh38.p7	15:63712878	ACTAGCCGGCTCTCT[A/G]CAGTAAGACTTTCAC	8925
rs375096759	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63693161	CCAGCCTGGGTGACA[G/T]GGTGAGACTCTGTCT	8925
rs375108021	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63619929	TATCAATTTTGTTGA[C/T]CTTTTCAAAAAACCA	8925
rs375114477	snp	C/T	0.000439198	0.0148124	synonymous-codon	HERC1	GRCh38.p7	15:63648126	TTCCTTTGTTCCCAG[C/T]AACAGTTTTCCATCA	8925
rs375118110	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63627429	GTAATCCCAGCACTT[C/T]GGGACGCTGAGGCTT	8925
rs375135750	snp	C/T	0.000121757	0.00780152	synonymous-codon	HERC1	GRCh38.p7	15:63645512	CTGCAACTTGGATCC[C/T]TTCCCTGGAAGGCGG	8925
rs375169418	snp	C/T	0.00016595	0.00910756	synonymous-codon	HERC1	GRCh38.p7	15:63674775	TTCCACACTTGGCAG[C/T]GTTGGATCTAAAGAA	8925
rs375184943	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63776037	AGCGAGACTCCGTCT[A/C]AAAAAAAAAAAAAAA	8925
rs375198275	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63626704	AGACTACAAGGCCTG[A/C]AGCCACAGCTACCCT	8925
rs375212901	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63660060	GCGATGGCTCACGCC[C/T]GTAATCCCAACACTC	8925
rs375226135	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63776313	CTACCAGTACCACCA[A/C]CCCACCCAAACCTGT	8925
rs375273758	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63790470	GTAGTCCCAGCTACT[G/T]GGGAAGCTGAGGCAG	8925
rs375275073	snp	A/C	3.48809e-05	0.00417603	missense	HERC1	GRCh38.p7	15:63634886	CTTGAAGCCACAAGA[A/C]ATCTAAGACAGAACC	8925
rs375280658	in-del	-/A	0.0809769	0.184204	intron-variant	HERC1	GRCh38.p7	15:63659245	GGTATCATGAAAGAC[-/A]AAAAAAAATCAAAAC	8925
rs375283342	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63781065	CAGAAAAAGTATCAT[C/G]TGTTAGGTAATAAAT	8925
rs375295782	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63808124	AGTAATTCTAGTTGA[A/C]AAAAAAAAAAAAATA	8925
rs375298173	snp	C/T	1.65875e-05	0.00287984	synonymous-codon	HERC1	GRCh38.p7	15:63624199	CTGAGGTCCATAGTT[C/T]TTGCCTTGAACCATG	8925
rs375304469	snp	C/T	4.31053e-05	0.00464228	missense	HERC1	GRCh38.p7	15:63643496	TCCGAACAGGAGTGA[C/T]GTGTCCCCGCAGCTG	8925
rs375307824	snp	C/T	1.658e-05	0.00287919	synonymous-codon	HERC1	GRCh38.p7	15:63635964	TTCCTGCCTGACCTG[C/T]ACCACTTCTTCTCCT	8925
rs375308854	snp	C/T	4.97022e-05	0.00498484	synonymous-codon	HERC1	GRCh38.p7	15:63640212	AACGGTAAAAGATTC[C/T]GGAAACTGGGCTCCA	8925
rs375309992	snp	A/C/G	0.000114433	0.00756344	missense	HERC1	GRCh38.p7	15:63672523	AGAGGCATCACTCCC[A/C/G]GGGACTCGGATGCAG	8925
rs375311813	snp	A/G	3.3557e-05	0.00409602	missense	HERC1	GRCh38.p7	15:63656299	ATTAATCGAACTAGC[A/G]TTCGGATATCTGTTA	8925
rs375324400	snp	C/T	1.65649e-05	0.00287788	missense	HERC1	GRCh38.p7	15:63713446	TCATCTATCACAGGA[C/T]TTACTCCTAATATTA	8925
rs375326118	snp	C/T	1.71728e-05	0.00293021	intron-variant	HERC1	GRCh38.p7	15:63656366	TGGAACCACTGCCAG[C/T]AAAGAAAAACATCTC	8925
rs375326418	snp	C/T	1.76708e-05	0.00297239	missense	HERC1	GRCh38.p7	15:63734797	AATTCCATCCGTTCT[C/T]GTAATGGAGGTAACA	8925
rs375333370	snp	A/G	0.000167986	0.00916323	synonymous-codon	HERC1	GRCh38.p7	15:63690598	CAGCACAGCTTCAAG[A/G]ACATGAAGTGCAAGG	8925
rs375333702	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63751136	TATCATATACACTCA[G/T]GCACCATTCGGTCAA	8925
rs375337283	snp	C/T	1.65658e-05	0.00287795	synonymous-codon	HERC1	GRCh38.p7	15:63775105	CATCCAACTTTGTCT[C/T]AGAAGCGCAAATAAT	8925
rs375350975	snp	G/T			missense	HERC1	GRCh38.p7	15:63656167	GCTGTGCTCAAATAG[G/T]CCAGGCAAGAGATAG	8925
rs375370883	snp	A/C/G			intron-variant	HERC1	GRCh38.p7	15:63690779	TTTCAAACTATTATC[A/C/G]CAAGAATTCTGGATC	8925
rs375372024	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63824845	CAAGTCAGACGTAGG[-/A]AAAAAAAAAAACACT	8925
rs375378579	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63635629	AGGTTAAAAGCAAAG[G/T]TTTCCTTTTATCTGT	8925
rs375386857	snp	A/G	0.0240643	0.107019	intron-variant	HERC1	GRCh38.p7	15:63708725	TTTCATTTACGAACA[A/G]TTCAGAATAAATGAG	8925
rs375392442	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63647278	AATTTACATTAAAAG[-/A]AAAAAAAAAAACACA	8925
rs375399482	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63782852	CCCCTACGGATGACT[C/T]TGAGAGGTTCAAGAC	8925
rs375403633	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63799712	GATAGGACAATAAAA[C/T]GCCAAAAAATAATGG	8925
rs375408290	in-del	-/CTTT			intron-variant	HERC1	GRCh38.p7	15:63746017	AATTGTTTTTCTGTT[-/CTTT]ATTTTTTTAATTTCA	8925
rs375410889	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63749024	TTAAACATTAAATCA[A/G]TAAAGCCTAGTTCTG	8925
rs375418502	snp	C/G	1.66029e-05	0.00288117	intron-variant	HERC1	GRCh38.p7	15:63661065	CATTTTTATATAAAA[C/G]AGTTAGTACCCCAAG	8925
rs375421649	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63632920	CAAAAATACTAATTG[C/T]CACTTACCTGTTCGA	8925
rs375426648	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63758533	TACTCATATGGAATA[A/G]ACCACTAAAAGACGC	8925
rs375441017	snp	A/G	0.000304945	0.0123442	intron-variant	HERC1	GRCh38.p7	15:63694563	TTCTAAAAGACAAAG[A/G]GACAGTTAAGAATCT	8925
rs375441661	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63796014	ATATTTAGGCTAAAT[G/T]GTGGGAGCTAAGAAC	8925
rs375449836	snp	A/G	0.000165986	0.00910854	intron-variant	HERC1	GRCh38.p7	15:63754654	TCACCATGACCTTGG[A/G]TAAAACACACACAAC	8925
rs375451665	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63800307	AATCTCTCCTCTGAC[A/G]AGAAGGCCAAGAACT	8925
rs375461409	snp	G/T	0.000165986	0.00910855	intron-variant	HERC1	GRCh38.p7	15:63666159	CTAGCACCTATACAG[G/T]GGAAAAACAGTCTGA	8925
rs375462454	snp	C/G			upstream-variant-2KB	HERC1	GRCh38.p7	15:63834888	CAAAAAATAGAGTTG[C/G]CCTCTGCGTTCCAGA	8925
rs375477932	snp	A/G	0.000173985	0.00932534	missense	HERC1	GRCh38.p7	15:63706794	CCTCTCTTTCTGTGA[A/G]ATGCTGCCAAATCCA	8925
rs375480026	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63629376	TGACTAAACACATCC[C/T]TGGATTCCACTTACG	8925
rs375485591	snp	C/T	8.79763e-05	0.00663177	missense	HERC1	GRCh38.p7	15:63775614	TCACTGGTGGAATCA[C/T]AGTTGCCATGTTGAT	8925
rs375493399	snp	C/T	4.97682e-05	0.00498815	intron-variant	HERC1	GRCh38.p7	15:63729490	TAAAAGACAAATAAT[C/T]GCATACCTCACTAAT	8925
rs375497427	snp	A/G	1.6974e-05	0.0029132	synonymous-codon	HERC1	GRCh38.p7	15:63774717	GCCTCATCTGCATTA[A/G]TATGGTCATAAAGCA	8925
rs375499946	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63787960	GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA	8925
rs375549428	snp	C/T	1.71941e-05	0.00293202	missense	HERC1	GRCh38.p7	15:63641510	AGCATCATGGGGAGC[C/T]GCTCCAAAAATGCTC	8925
rs375556560	snp	C/T	1.65726e-05	0.00287855	missense	HERC1	GRCh38.p7	15:63666051	CTAGAGTCTGCTGTG[C/T]TGCCCGACTGGGGCT	8925
rs375563587	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63765680	TATGACCTGGAAGCC[C/G]CCCACCTCGAGTTAT	8925
rs375595382	snp	A/G	0.000421186	0.0145057	synonymous-codon	HERC1	GRCh38.p7	15:63749756	AGCTTCTGAAGAACC[A/G]CAACCTAGACAAGCT	8925
rs375634665	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63713750	AATAGTCAAAAAGTT[C/T]GGACCAAAAACTTAC	8925
rs375654618	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63763787	AAGGGTATTTATTTT[A/G]TAATAATTCATTAAG	8925
rs375659805	snp	A/G	5.27134e-05	0.00513361	missense	HERC1	GRCh38.p7	15:63641618	GCAGCTGCCCATTCT[A/G]CTGTACAATTCACGA	8925
rs375667433	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63731566	GCCATTACTCCTTAA[C/T]ATCAGATTAAATTTA	8925
rs375674369	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63645192	GATCTGATAGAACCA[C/T]TGCATTATTTTTTAA	8925
rs375693017	snp	C/T	1.77112e-05	0.00297578	synonymous-codon	HERC1	GRCh38.p7	15:63674592	AACTTTTGGTATCAG[C/T]AACAGCTCAGCATAT	8925
rs375695183	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63734386	ACTCTTTATACAAAC[A/G]ATTTCAGACAAAGTT	8925
rs375698720	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63680516	AAGAAAAATGTAATG[C/G]TTGTGAATGGGTGTC	8925
rs375701308	snp	A/T	1.68496e-05	0.0029025	missense	HERC1	GRCh38.p7	15:63716457	TCAACATCTGCAGAG[A/T]CCTGGTTTTCTGATA	8925
rs375721003	snp	A/G	0.000159987	0.00894249	missense	HERC1	GRCh38.p7	15:63626022	AGCAGTCTCCAGGAT[A/G]AGTACATGAGGTCAG	8925
rs375728607	snp	C/T	3.36905e-05	0.00410416	intron-variant	HERC1	GRCh38.p7	15:63716273	GCATGCCACAGTTTG[C/T]ATCTAGAAAGTAAGA	8925
rs375730812	snp	C/T	3.68385e-05	0.00429161	intron-variant	HERC1	GRCh38.p7	15:63652378	TGTTTAGGATTCTCT[C/T]ATTTTAAATGGTATA	8925
rs375753293	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63813927	AGCAGGGCATGGTGG[C/T]GGGTGCCAGTAATCC	8925
rs375787266	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63615994	TTTACATACAAATAC[A/G]GCACAGCAATAACAA	8925
rs375843350	snp	A/C	8.28603e-05	0.00643609	missense	HERC1	GRCh38.p7	15:63775136	AAACTTAGACCAGTT[A/C]GAACACCCATTTCTA	8925
rs375859669	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63790778	CACAGTAGGGTTTTC[-/T]TTTTTTTTTTTTTTA	8925
rs375910680	snp	C/T	1.66106e-05	0.00288184	missense	HERC1	GRCh38.p7	15:63630602	GGTCGATTGTGATTG[C/T]GAGCACGCCCCTCTG	8925
rs375911709	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63787865	AGCTGGGGAGGCATA[C/T]TGGGGAGGCCGCCTG	8925
rs375915620	snp	C/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63745736	GCTCACCTGATTTTT[C/G]GTTCTTATGAAGGTG	8925
rs375917148	snp	A/C	0.00665556	0.0573017	synonymous-codon	HERC1	GRCh38.p7	15:63654272	CCGATGCTGTGAGGA[A/C]AGCCTGGAGGAGAGG	8925
rs375922313	snp	C/T	1.65751e-05	0.00287876	synonymous-codon	HERC1	GRCh38.p7	15:63686398	TACTCCTGTAGATGC[C/T]AATCCATATCCTTTC	8925
rs375922721	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63807044	AGCCACCACACCCGG[C/G]CTGAGTGATTTTTTT	8925
rs375927225	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63827287	ATTAGCCAGGTATAG[C/T]GGTGCACACTTGTAG	8925
rs375935028	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63780647	GAATGGTGTGAACCC[A/G]GGAGGCGGAGGTTAC	8925
rs375937848	in-del	-/A	0.405776	0.195535	intron-variant	HERC1	GRCh38.p7	15:63786277	GATCATGTTTCTATT[-/A]AAAAAAAAAAAAAAA	8925
rs375951174	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63817396	TCTGAAAGGTAAACA[C/T]TACGTATGTCAAGGA	8925
rs375951435	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63663835	AAAAATCAGTTACCT[C/T]AATTATATGAGAAAT	8925
rs375962075	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63618905	TTTGGGATGAGATGA[C/T]GGGGTTTTCTAGATA	8925
rs375963676	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63725019	ATAAGTGATGAAGCA[C/T]TGAGTTAGATGACTT	8925
rs375968062	snp	C/G	4.9694e-05	0.00498443	missense	HERC1	GRCh38.p7	15:63686475	ACTGAGCTTTCTCCG[C/G]GTCAAAGGATACTTC	8925
rs375971299	snp	A/G	1.65649e-05	0.00287788	missense	HERC1	GRCh38.p7	15:63733010	TCTGAGTGCCGTAAG[A/G]TTGATCTGACAGATT	8925
rs375971455	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63620198	GGTATGTTGTGTCTT[C/T]GTTCTCGTTGGTTTC	8925
rs375973798	in-del	-/AGTACTACC/ATGAATAGTACTACC	0.0248432	0.108648	intron-variant	HERC1	GRCh38.p7	15:63656974	CAACATGGGGCTATT[-/AGTACTACC/ATGAATAGTACTACC]ATGAATAGTACTACC	8925
rs375981726	snp	A/C/G	6.62837e-05	0.00575657	synonymous-codon	HERC1	GRCh38.p7	15:63640200	TTCTAGATCTGGAAC[A/C/G]GTAAAAGATTCTGGA	8925
rs375989768	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63706105	AGTTTTTAGTTATCA[C/T]TGGATTTACACTATC	8925
rs376003661	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63611579	CCTTCTGGGGCACAC[A/C]CACCAGTTAATGGTT	8925
rs376017271	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63744172	TGTGTGTGTCTCTCT[C/G]TCTCTCTCTCTCTCT	8925
rs376033397	snp	A/T	1.65721e-05	0.0028785	missense	HERC1	GRCh38.p7	15:63640368	CAACAGCTGATCCAG[A/T]TGAAGTCCCACAGCA	8925
rs376035697	snp	A/C/G	3.79142e-05	0.00435384	utr-variant-3-prime, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609079	TGAGAGCACCCGCAC[A/C/G]GTCAGTAGTCAGTGT	8925
rs376055342	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63768020	CCACCCCATTAATAA[C/T]CATTATTCTTAATTA	8925
rs376058656	snp	C/T	7.06714e-05	0.00594396	synonymous-codon	HERC1	GRCh38.p7	15:63641521	GAGCCGCTCCAAAAA[C/T]GCTCTCATGCAGGGA	8925
rs376060804	snp	A/G	0.000119365	0.00772451	missense	HERC1	GRCh38.p7	15:63696332	TGATGAAGTGCCTCT[A/G]AACGAAGCTTGAGGA	8925
rs376062287	in-del	-/T/TT/TTT			intron-variant	HERC1	GRCh38.p7	15:63743263	CTTTTTTTCTTTTTC[-/T/TT/TTT]TTTTTTTTTTTTTTT	8925
rs376065765	snp	C/T	1.6599e-05	0.00288084	missense	HERC1	GRCh38.p7	15:63666081	TCCTCTTCATCCTCA[C/T]GCCCAGGGTGCTCTA	8925
rs376090615	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63831221	AATTGATCCTCCCAT[A/C]TCAGCCTCCCTAATA	8925
rs376102246	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63756268	ATAAGAATTAAAATT[C/T]AATAATGTATACAAA	8925
rs376131292	snp	C/G	1.65902e-05	0.00288008	intron-variant	HERC1	GRCh38.p7	15:63638789	ATCCTGAAAAACAGG[C/G]GGTACATAATGATCA	8925
rs376140607	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63772337	GGTAACTAGCATTTT[A/G]TTCAAACACACCATT	8925
rs376141616	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63754735	ATAATAAATGTTACA[A/C]CTTTAAAATAGAATT	8925
rs376143004	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63660542	TAATAGAGGTTTAAA[C/G]TAATTAAAAATATTG	8925
rs376171992	snp	A/G	0.000232724	0.0107846	synonymous-codon	HERC1	GRCh38.p7	15:63615894	GCCATCAGCACTCTG[A/G]CCAACAAAAGAATCA	8925
rs376175546	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63732260	CCCAACTCGGCCTCC[C/G]AAAGTGCTGAGATTA	8925
rs376178804	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63705927	CCCAGCTACTTGGGA[A/G]GCTGGAGTAGGAGGA	8925
rs376187755	snp	C/T	1.658e-05	0.00287919	synonymous-codon	HERC1	GRCh38.p7	15:63713394	GGCACTTGTTGAAGG[C/T]TGCTGCAACTGTCCT	8925
rs376187990	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63824479	GCAGAGGTTGCAGTG[A/G]GCTGAGATCATGCCA	8925
rs376192663	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63756388	CGACATTGTCAATTA[C/T]AACTCCAATGCATCT	8925
rs376195217	snp	A/C/G	0.0229296	0.104591	missense, synonymous-codon	HERC1	GRCh38.p7	15:63775396	GGCATCCAAATAGTG[A/C/G]TCCTGCTCATCACTT	8925
rs376197956	snp	A/C	0.000167986	0.00916323	intron-variant	HERC1	GRCh38.p7	15:63645133	AAAACCAAAACATGT[A/C]AATATGCATTAAGTA	8925
rs376211444	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63728147	TTATAATTTACTCAA[A/G]AAATATTTATTTACT	8925
rs376224518	snp	A/C	0.000391053	0.0139776	intron-variant	HERC1	GRCh38.p7	15:63680199	AAAGAAAAAGGAAAT[A/C]GAAATTTTTTTAATT	8925
rs376234542	snp	A/C	3.77202e-05	0.00434266	synonymous-codon	HERC1	GRCh38.p7	15:63729267	AACACTGCCATTCCA[A/C]GGACTTTCTTTGAGC	8925
rs376235781	snp	C/G/T	0.000115516	0.00759909	synonymous-codon	HERC1	GRCh38.p7	15:63764144	GGAGCACAAGCCATC[C/G/T]GATGTTCTGGTTGGT	8925
rs376271895	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63614122	GACCAATTCATATAT[A/G]AAGAAAGAGGAGGAA	8925
rs376280658	snp	A/G	0.000331526	0.0128706	missense	HERC1	GRCh38.p7	15:63723350	ACAGGCAACTCATAC[A/G]TTTATCTAAAAAAAA	8925
rs376289801	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63731918	AACAACAGGAAATAC[A/G]TGTACAATGTACAAT	8925
rs376299394	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63730963	AAAGAAAGTGACTGC[C/T]ACTATAATATTTTTT	8925
rs376313734	in-del	-/ACTA			intron-variant	HERC1	GRCh38.p7	15:63750360	AATACCAAAAGAATC[-/ACTA]ACTGATTTAAGATGC	8925
rs376314696	snp	C/G/T	8.30446e-05	0.00644333	missense	HERC1	GRCh38.p7	15:63622868	AGAGGGTATAAGAAG[C/G/T]TCAACAATACCAGTT	8925
rs376315533	snp	A/G	4.39628e-05	0.00468823	synonymous-codon	HERC1	GRCh38.p7	15:63652473	GGTAACATTCCATAC[A/G]CGGATGGTGCCATCA	8925
rs376321276	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63829462	TGTGTGTGTGTGTGC[A/G]CATATATGTTTATAT	8925
rs376321729	snp	A/G	0.000213261	0.010324	intron-variant	HERC1	GRCh38.p7	15:63641432	ATTCCAAAGCACCAG[A/G]TATCTGTGTATCTCT	8925
rs376321930	snp	A/T	4.95307e-05	0.00497623	synonymous-codon	HERC1	GRCh38.p7	15:63648135	TCCCAGTAACAGTTT[A/T]CCATCAAAATATCCC	8925
rs376323982	snp	C/T	0.000149074	0.00863221	missense	HERC1	GRCh38.p7	15:63674932	TCCTCGGATTCATGT[C/T]GGTGTTTCTTTTCAT	8925
rs376338296	snp	A/C	0.000163987	0.00905353	intron-variant	HERC1	GRCh38.p7	15:63677821	AATATTTGTTTGCTA[A/C]AAGTGTAACTCAACA	8925
rs376342493	snp	A/G/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63737391	ATATATATATATATC[A/G/T]TTTTTCCAGATATAT	8925
rs376343657	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63783256	CAGCAAACTTCACTG[C/T]TGTCTTGTTTTAATA	8925
rs376346394	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63617779	GATGAGCATTTTTTC[A/G]TGTGTCTTTTGGCTG	8925
rs376391409	snp	C/T	0.000167986	0.00916322	intron-variant	HERC1	GRCh38.p7	15:63640147	GCAGCTCACAGTACA[C/T]TTACCATTAGAAATA	8925
rs376400003	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63611863	CCTACTTGAGGGTCA[C/T]AGTTTGTTTTCCCCA	8925
rs376400593	snp	C/T	0.000163987	0.00905353	synonymous-codon	HERC1	GRCh38.p7	15:63649825	CCGTCCCACCAACAA[C/T]AATTCTGGAGACTCT	8925
rs376409443	snp	A/G	1.65658e-05	0.00287795	missense	HERC1	GRCh38.p7	15:63661984	TCACACAGTTCACAC[A/G]CCACCACTTCTTCCC	8925
rs376413220	snp	A/G	3.10082e-05	0.0039374	intron-variant	HERC1	GRCh38.p7	15:63696085	GTGGCTTTGTAAAAT[A/G]ACAGTTAAAATCTGT	8925
rs376415661	snp	C/T	6.62987e-05	0.00575717	synonymous-codon	HERC1	GRCh38.p7	15:63678039	CCTCAGCTGCAGCTC[C/T]GAGAGGTCAGCGAGG	8925
rs376415713	snp	C/T	0.0029606	0.0383606	synonymous-codon	HERC1	GRCh38.p7	15:63775003	GCTTTCATTTGCTAA[C/T]GATAATGGTGGCAAA	8925
rs376418299	snp	C/G	6.64706e-05	0.00576462	missense	HERC1	GRCh38.p7	15:63725326	TTCTACACCGTCACT[C/G]AACAGTGGCGTTTTC	8925
rs376425767	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63752691	TAGAAAAGGTTTAAG[A/G]GAAGCTAAATGCTAA	8925
rs376427330	snp	C/G	0.000167986	0.00916323	missense	HERC1	GRCh38.p7	15:63756538	CCCAACTGAAGACTT[C/G]TCCTTCTGTCGTAAA	8925
rs376427652	snp	C/G	1.67033e-05	0.00288987	intron-variant	HERC1	GRCh38.p7	15:63725542	CATTAGTTATTGTGT[C/G]TTTATCTGGTACTTT	8925
rs376439205	snp	C/T	0.00636936	0.0560724	intron-variant	HERC1	GRCh38.p7	15:63737607	CTGGTCTTCAATTCC[C/T]GGCCTCAGGTGGTCC	8925
rs376444098	snp	A/G	0.000165986	0.00910854	missense	HERC1	GRCh38.p7	15:63637591	CCTTCCCCACAAGCC[A/G]ACACTGTGCCATTGG	8925
rs376466663	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63622021	CGTCCAGCTTTGTTC[C/T]GTTGCTGGTGAGGAG	8925
rs376478254	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63625693	AGTGAGACTCCATCT[A/C]AAAAAAAAAAAAAAA	8925
rs376481932	snp	C/T	1.65778e-05	0.002879	missense	HERC1	GRCh38.p7	15:63678050	GCTCTGAGAGGTCAG[C/T]GAGGCCATGCCTAGT	8925
rs376484883	snp	A/T	0.000337943	0.0129945	intron-variant	HERC1	GRCh38.p7	15:63747132	TCATAAAAGTGCCTG[A/T]GCTATCCAGTTTGGG	8925
rs376495434	snp	C/G	0.000188987	0.00971893	missense	HERC1	GRCh38.p7	15:63764163	GTTCTGGTTGGTTCT[C/G]TCCACTGACTCCGAT	8925
rs376522641	snp	A/G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63724834	GGCACTTTAAGTGGC[A/G/T]AAGAAAAAATTAGGA	8925
rs376571939	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63742144	TTTCCATTTATTTCG[A/G]TCTTCTTTAATTTCT	8925
rs376584426	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63624604	GGAGGCTGAGGTGGG[C/T]GGATCACCTGAGTCC	8925
rs376591272	snp	A/G	4.96808e-05	0.00498377	synonymous-codon	HERC1	GRCh38.p7	15:63636018	CCGCCGCTGCCTGTC[A/G]CTGTTCCCATGGCCA	8925
rs376599580	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63662929	TGTTAGTAAGCTATA[G/T]GAACAGGAGGGCAGG	8925
rs376602356	snp	C/G/T	0.000190517	0.00975854	intron-variant	HERC1	GRCh38.p7	15:63706849	ATTAAAAGTAAAAAG[C/G/T]AAATAAATAAAATTT	8925
rs376623869	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63636219	AGCTGCTACTGAATA[A/C]CCTCAATCAAAAACC	8925
rs376664035	snp	A/G	0.000298028	0.0122035	synonymous-codon	HERC1	GRCh38.p7	15:63661947	TCTCTTCATGTGCTG[A/G]TTGAAGCTGACGACG	8925
rs376674111	snp	C/T	0.000138169	0.00831057	intron-variant	HERC1	GRCh38.p7	15:63712728	GCCTTACATATCATA[C/T]ACCTTGAAAACAAAA	8925
rs376682180	snp	C/G	1.65663e-05	0.002878	missense	HERC1	GRCh38.p7	15:63694803	TTTGCTTGCAGGGCT[C/G]TTTCCAGGGTAGCAG	8925
rs376686768	snp	A/G	1.68306e-05	0.00290087	missense	HERC1	GRCh38.p7	15:63755321	GCTGACACACAAACA[A/G]CTACCTGCATTGCAC	8925
rs376687657	snp	A/G	0.000124291	0.00788226	intron-variant	HERC1	GRCh38.p7	15:63756387	ACGACATTGTCAATT[A/G]CAACTCCAATGCATC	8925
rs376689142	snp	A/G	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63802094	CTGAAAGTGCAGGAG[A/G]AAGAGCCCATTTGCA	8925
rs376723494	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63711928	TGAAAACCTAGCTAC[C/G]AATTAACTCCAAGTC	8925
rs376739060	snp	C/G/T			intron-variant	HERC1	GRCh38.p7	15:63697744	ACAGGAGTGAGCCAC[C/G/T]GCGCCCGGCCAATCT	8925
rs376755573	snp	A/C	1.65949e-05	0.00288048	missense	HERC1	GRCh38.p7	15:63674783	TTGGCAGTGTTGGAT[A/C]TAAAGAAAATGAAGC	8925
rs376771585	snp	C/T	5.29806e-05	0.0051466	missense	HERC1	GRCh38.p7	15:63775617	CTGGTGGAATCATAG[C/T]TGCCATGTTGATTTA	8925
rs376778502	snp	A/G	0.000167986	0.00916322	synonymous-codon	HERC1	GRCh38.p7	15:63666387	TTTGGCAATCTGCCG[A/G]AGAGAGAACCCCATT	8925
rs376781545	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63721504	GCACTCCAGCCTGGA[C/T]GATAAGAGGAGACTC	8925
rs376796383	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63646953	TAATCATCAGAGAAA[A/C]GCAAATTCAAACCAC	8925
rs376809614	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63721989	CTTTAGCCTCCCGAG[C/T]AGCTGGGATTACAGG	8925
rs376830508	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63786947	TTTATTTTTTGAGAC[A/G]GAGTTTCACTCTTGT	8925
rs376844151	snp	A/G			missense, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609142	AGCATGTAGTTGTCC[A/G]TGTCGATTGAGCGGC	8925
rs376860866	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63829244	GGCAAAACAGCAGGA[A/C]CTCGTCTCTACTAAA	8925
rs376899719	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63787244	TCACTGCAACCTCCG[A/C]CTCCAGGATTCAAGC	8925
rs376905628	snp	A/G	0.000215355	0.0103745	synonymous-codon	HERC1	GRCh38.p7	15:63680606	AATGAAATCTCCTTG[A/G]GTAAAGCTGGACAAT	8925
rs376919603	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63817149	AGAGTCTAAAGATTT[A/T]AAATGATGTAATAAA	8925
rs376932970	snp	A/C	1.65734e-05	0.00287862	intron-variant	HERC1	GRCh38.p7	15:63733149	CAGTTGCATTCTCTA[A/C]AGAACAATAAAATAG	8925
rs376933014	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63654650	CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC	8925
rs376949519	snp	C/G	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63772955	AAAAGTAGGTGAAAA[C/G]TTAAATGTCCCTGGT	8925
rs376959351	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63743204	TGTGCTTCAACCTTT[C/T]TTATTCTTTTTCTTT	8925
rs376973876	snp	A/G	4.97162e-05	0.00498554	missense	HERC1	GRCh38.p7	15:63638472	TTTCTTCCAGCTTCT[A/G]CCAGCTGTCCATGCC	8925
rs376999823	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63631533	CAGCTCTCCCAATTC[C/T]TCTTCTTTTTAATCT	8925
rs377016285	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63707046	TGAAACACTAACTAA[A/G]AAACTCACATTAATT	8925
rs377048686	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63619380	AAGCTTTTTGATGTG[C/T]TGCTGGATTCGGTTT	8925
rs377061817	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63698286	AGCCAAGCATGGTGG[C/T]GCATGCCTATAATCT	8925
rs377072857	snp	A/G	4.78847e-05	0.00489286	intron-variant	HERC1	GRCh38.p7	15:63622784	TTATTATTATTTTAG[A/G]CATATAATGAACACT	8925
rs377074161	snp	C/T	0.000348123	0.0131886	intron-variant	HERC1	GRCh38.p7	15:63638688	CTGAGAACCATCATA[C/T]AGTTATCTTCATCTT	8925
rs377086611	snp	C/T	0.000159987	0.00894248	synonymous-codon	HERC1	GRCh38.p7	15:63661797	CTTCATGGCTAAGTA[C/T]TTCTCCCTGCAGGTG	8925
rs377124732	snp	A/C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63702583	AATCGTACAACCATA[A/C/G]CAAATCTTTTAAGTT	8925
rs377125296	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63784305	CCACAGTTCTAGCCA[C/G]AAAGTAGTGAAACCA	8925
rs377126091	snp	A/C/T			intron-variant	HERC1	GRCh38.p7	15:63750547	TTATATAGATTCTTA[A/C/T]CTTCATGCCATCAAA	8925
rs377128369	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63692280	TTTTGATCAAATAGG[C/T]ACGCAGAAAATAAGA	8925
rs377130232	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63730341	GTGCACACCTCTAGT[C/T]CCAGCTACTTGGGAG	8925
rs377131166	snp	C/G	0.000161987	0.00899818	missense	HERC1	GRCh38.p7	15:63640292	AGGCCCATTCATTTG[C/G]ATTCCAGGATGCAGG	8925
rs377134198	snp	A/C	0.000165986	0.00910854	intron-variant	HERC1	GRCh38.p7	15:63616387	CTAGTCTGTGCATAT[A/C]GGACGTCAACACCAG	8925
rs377135470	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63790305	CTTTTTAGGCTAGGC[A/G]CGGTGGCTCATGCCT	8925
rs377137482	snp	C/G/T	4.98155e-05	0.00499056	missense, synonymous-codon	HERC1	GRCh38.p7	15:63624277	TAACAAAGGCCGAAG[C/G/T]TGTCCCTGTACAATG	8925
rs377138267	snp	A/T	3.33856e-05	0.00408555	missense	HERC1	GRCh38.p7	15:63651372	AGGCTTTCCTCAGCA[A/T]CCCCTTCCCTAGAAT	8925
rs377139162	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63798011	CTCTAAATGTTGAGT[A/G]GATGTGAATGAGAAT	8925
rs377143144	snp	C/T	6.63713e-05	0.00576032	synonymous-codon	HERC1	GRCh38.p7	15:63616454	ACTCTCCTCGGTAAT[C/T]CCACTGTCTTCAATG	8925
rs377147575	snp	C/T	6.99191e-05	0.00591225	synonymous-codon	HERC1	GRCh38.p7	15:63696220	CTGCAGCCTCACAGA[C/T]GTGAGTAGTGTGGAG	8925
rs377157760	snp	G/T	1.65715e-05	0.00287845	missense	HERC1	GRCh38.p7	15:63758211	AGGAGCCAGTTTGGG[G/T]TGCAGTATTTTCTCC	8925
rs377161088	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63680266	TGAGACAGAACAAAA[C/G]TTACTAGATCAAATT	8925
rs377162726	snp	C/G	0.00835141	0.0640778	intron-variant	HERC1	GRCh38.p7	15:63707560	CTTGTGCATAGACTT[C/G]ACATTATGGTATCAG	8925
rs377169413	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63667688	CCTTAAGGTGATATT[A/G]TACCACTTCATATGT	8925
rs377195733	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63833749	AAAGCACACACGCGC[A/G]CGCGCACACACACAC	8925
rs377205858	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63617231	TGTTCTCATTGTTCA[A/G]TTCCCACCTATGAGT	8925
rs377207335	snp	C/T	1.65864e-05	0.00287974	synonymous-codon	HERC1	GRCh38.p7	15:63774775	TGAGAGTAGTTTGCC[C/T]TTCTCCATGGTGTGT	8925
rs377210174	snp	C/T	4.52478e-05	0.00475625	missense	HERC1	GRCh38.p7	15:63723206	CAGCATAGTCCTGCA[C/T]GCTGATCCAAAGGCT	8925
rs377229684	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63673630	TACAAGATAAAACAG[A/G]GCTTTTCTTTTTTTA	8925
rs377241829	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63812118	CCATAAACATAGACA[C/T]TAAGTTGCCTACCCT	8925
rs377273877	snp	C/T	2.65573e-05	0.00364389	missense	HERC1	GRCh38.p7	15:63622836	CTATTGTAACCCACT[C/T]CTGCGGTGGCATTGG	8925
rs377277865	snp	A/G	1.65817e-05	0.00287933	synonymous-codon	HERC1	GRCh38.p7	15:63638528	ACATTTACCTCCCAG[A/G]TGCCAGTCCTAGAAA	8925
rs377322807	snp	A/T	0.000236351	0.0108683	intron-variant	HERC1	GRCh38.p7	15:63616414	CCAGTAGAAACATAG[A/T]CTGGCCAGGATTTAC	8925
rs377337124	snp	C/T	1.67812e-05	0.0028966	intron-variant	HERC1	GRCh38.p7	15:63636181	AGGAGTCACTGGATG[C/T]TAAAACTCTCCTCTT	8925
rs377337200	snp	C/T	2.03233e-05	0.00318767	intron-variant	HERC1	GRCh38.p7	15:63645471	ACGTATAGATGCAAA[C/T]TGACAACATACGTAG	8925
rs377344540	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63636274	GAATAATTTCATTAG[-/T]TTTTTTTTTTTTTTT	8925
rs377346681	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63805025	ACTGCTTGGCAGTTT[A/G]TCATAAACACACGCT	8925
rs377348535	snp	A/G	0.000419791	0.0144817	synonymous-codon	HERC1	GRCh38.p7	15:63694046	TTGCTCCCCTTCTCC[A/G]AAAGAGGCCATATGT	8925
rs377350622	snp	C/T	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63826214	CTGGGCAGCACTTGT[C/T]ACCCTAAAAGATGGG	8925
rs377350692	snp	C/T	0.000169986	0.00921759	intron-variant	HERC1	GRCh38.p7	15:63718533	AGCTAGCTCTCACAG[C/T]TTGCAGAAAAACATA	8925
rs377383316	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63665708	ATTATGAAATTTCTT[C/T]TGGCATGAAAACACC	8925
rs377384208	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63627225	TAGATATCTAAGAAA[C/T]AAAATCCCTATGGGG	8925
rs377395410	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63704456	TAAACTTAACTAATA[C/T]AGTATAAACTATAAA	8925
rs377398452	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63815499	GTGCCTGGATGTAGT[A/T]AATGTTACATAGTGA	8925
rs377404008	snp	C/T	1.70936e-05	0.00292344	intron-variant	HERC1	GRCh38.p7	15:63755338	TACCTGCATTGCACA[C/T]AAGTAAATACGATGA	8925
rs377406224	snp	A/G	0.000153932	0.00877167	intron-variant	HERC1	GRCh38.p7	15:63690536	ATAATTTTAAAAATA[A/G]AAACCTGGGCCATTT	8925
rs377417946	snp	C/T			downstream-variant-500B, utr-variant-3-prime	HERC1, FBXL22	GRCh38.p7	15:63608468	ATTTCCAAGTGAAGC[C/T]CACCCTCAATGTAAA	8925
rs377439130	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63632270	AATCTCAGTCCTACT[A/G]TGAATGCCTGGGTTA	8925
rs377451682	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63650651	AAAAACACTGAATGT[A/G]CAAATGTACAAATGT	8925
rs377454738	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63654782	GCTGAGGCAGGAGAA[C/T]TGCTTCAAGCTGGGA	8925
rs377455759	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63689471	GGAGACAGAATGCCA[A/G]GAGAGGAAATGGAAT	8925
rs377460066	snp	G/T	3.61298e-05	0.00425013	intron-variant	HERC1	GRCh38.p7	15:63612596	TCAATGAGTGTGCGT[G/T]AACCTGGCACCCACC	8925
rs377471286	snp	C/G	3.31241e-05	0.00406952	missense	HERC1	GRCh38.p7	15:63669622	CAGAAGGAGAGGTTG[C/G]TAACGAAGATATTGG	8925
rs377471691	snp	C/G/T	5.30812e-05	0.00515153	missense	HERC1	GRCh38.p7	15:63656209	TTGCTATGCCCACCT[C/G/T]GTGATCGTTCTGAGG	8925
rs377473680	snp	A/G	1.85187e-05	0.00304286	missense	HERC1	GRCh38.p7	15:63634758	TGATATCCCTCCAGT[A/G]CAGTCACTCTCTCTG	8925
rs377478362	snp	A/G	0.000310537	0.0124568	intron-variant	HERC1	GRCh38.p7	15:63712939	TTTTGATTTAGGACT[A/G]TTAGTGAACATAAAA	8925
rs377486779	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63672856	AAATATTCTTACTTA[C/T]ATACATCTTTGTATT	8925
rs377489615	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63650200	CTGAGGTCAGGAATT[C/T]GAGACCAGCCTAGTC	8925
rs377497125	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63790956	TGAAAGATATCTTTA[C/T]AGAAGGCTTGTTTTT	8925
rs377530502	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63688063	AATTTTAAAAGATCA[C/T]TCTGGATCCTGTGCA	8925
rs377533574	snp	A/G	2.02059e-05	0.00317845	missense	HERC1	GRCh38.p7	15:63694324	TACCCAGTAGTGATG[A/G]CTAGAATCTGGAGCA	8925
rs377537305	snp	A/G	5.51526e-05	0.00525103	missense	HERC1	GRCh38.p7	15:63718585	TTACCCATCTGTCCC[A/G]TGATGATGACCTTGT	8925
rs377539529	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63669511	AATGCCAACTTTGGA[C/T]ATCATAGTGCATATC	8925
rs377540016	snp	C/T	3.44276e-05	0.00414881	intron-variant	HERC1	GRCh38.p7	15:63729402	CCTAAATTACTACTT[C/T]GAAAGATTCAAGGTG	8925
rs377546517	snp	G/T	1.66568e-05	0.00288585	missense	HERC1	GRCh38.p7	15:63775546	TCTTGTAGCAATAGA[G/T]TCACTGTCCTCTGTA	8925
rs377560628	snp	A/C	8.29745e-05	0.00644052	synonymous-codon	HERC1	GRCh38.p7	15:63665954	CATTTCAGCAGCATC[A/C]GCTGATGGTATGTCT	8925
rs377561505	snp	C/G	0.00914312	0.0669923	intron-variant	HERC1	GRCh38.p7	15:63714813	CGGCCTCCCAAAGTG[C/G]TGGGATTACAGCCGT	8925
rs377586711	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63829573	TGTGTATATATATAT[A/G]TATATATATATATAT	8925
rs377589654	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63633565	CTGGAGATATGTTTC[C/T]AACTATTTCTTCCCT	8925
rs377592300	snp	C/T	4.97006e-05	0.00498476	synonymous-codon	HERC1	GRCh38.p7	15:63775111	ACTTTGTCTTAGAAG[C/T]GCAAATAATAAACTT	8925
rs377649950	snp	G/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63638947	TTGATTTTATGCACT[G/T]TCAGTATTTCCCTTT	8925
rs377667959	snp	A/C/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63671789	TGAAAATCGTAATGC[A/C/G]TTCTTAACTAAGGAA	8925
rs377680465	in-del	-/AT	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63742439	CATCCGCAAACAGAA[-/AT]AGTTTTACAACTTCC	8925
rs377685003	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63653354	AGGCTGAGGCAGGAG[A/C]ATCACTTGAACCCGG	8925
rs377685698	in-del	-/AATA			intron-variant	HERC1	GRCh38.p7	15:63660333	CAAAGAAATAAAAAC[-/AATA]AATAAATAAATAAAT	8925
rs377690860	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63832699	CAGTGAAAAAGATAG[C/T]GATGGCAGAGTTCAG	8925
rs377711475	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63801287	ACTCCCCCGTTTGTA[A/G]GCAATTCAGAAGTGT	8925
rs377712859	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63822185	ACGGATAGTTCAATG[C/T]AGCAGAAGTGGAATA	8925
rs377736630	in-del	-/CATTT			intron-variant	HERC1	GRCh38.p7	15:63767002	GTTTTATAGGTTTTT[-/CATTT]GTTTTTTTTTTTTGA	8925
rs377743596	snp	C/G	1.67953e-05	0.00289782	missense	HERC1	GRCh38.p7	15:63612544	AGGACATCCCTTCTC[C/G]GACTGCAGCCACCTG	8925
rs386383263	in-del	-/CTAT			intron-variant	HERC1	GRCh38.p7	15:63616252	TGCAGGAGCCTGCTC[-/CTAT]TATTAGAAGCTGTTT	8925
rs386383264	in-del	-/AT			intron-variant	HERC1	GRCh38.p7	15:63737547	ATATATATATATATA[-/AT]TCTTTTTTTTTTTTA	8925
rs386784770	in-del	A/TATAACTATGCAGTCCCGTAACT			intron-variant	HERC1	GRCh38.p7	15:63637779	AAAGGGAAGAGTTGA[A/TATAACTATGCAGTCCCGTAACT]CCTTGATGACTATAA	8925
rs386784771	multinucleotide-polymorphism	ATGGC/GTGGT			intron-variant	HERC1	GRCh38.p7	15:63642020	TTTAACTCTGGCTCT[ATGGC/GTGGT]TTATTCTACACAGGC	8925
rs386784772	multinucleotide-polymorphism	CAA/TAG			intron-variant	HERC1	GRCh38.p7	15:63642948	CATTTGATATAACTA[CAA/TAG]TATTACCTTTGATCT	8925
rs386784773	multinucleotide-polymorphism	CGG/TGC			intron-variant	HERC1	GRCh38.p7	15:63651756	AAACTATTAAAAATG[CGG/TGC]CTGGGCGTAGTGGCT	8925
rs386784774	multinucleotide-polymorphism	CCT/TCC			intron-variant	HERC1	GRCh38.p7	15:63668025	GGGTTGGTGCTGCAA[CCT/TCC]CTGCAATGTTCAAGG	8925
rs386784775	multinucleotide-polymorphism	AC/CT			intron-variant	HERC1	GRCh38.p7	15:63692901	TTCCCAAATATCAGG[AC/CT]AGGCGCAATGGCTCA	8925
rs386784776	multinucleotide-polymorphism	AA/TC			intron-variant	HERC1	GRCh38.p7	15:63732107	CCTGGTTCAAGCAAC[AA/TC]TCCCACCTCGGCCTC	8925
rs386784777	in-del	AG/TAA			intron-variant	HERC1	GRCh38.p7	15:63790622	TTTTAAATACTAGAA[AG/TAA]TAGACACCCAAACTC	8925
rs386784778	multinucleotide-polymorphism	GTATATTAAGGTCAGTTTTTTATAC/TTATATTAAGGTCAGTTTTTTATAA			intron-variant	HERC1	GRCh38.p7	15:63798826	AATGGTAACTCATAG[lengthTooLong]GCCCTAAGCATTTAG	8925
rs397704369	in-del	-/A	0.375	0.216506	intron-variant	HERC1	GRCh38.p7	15:63695403	GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA	8925
rs397742101	in-del	-/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63648660	CTCACAATCTATATT[-/T]CTACTTGTTTCTTCA	8925
rs397802816	in-del	-/A	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63760455	AAAAAAAAAAAAAAA[-/A]GACACAAAGGAAAAA	8925
rs397804680	in-del	-/G			intron-variant	HERC1	GRCh38.p7	15:63673629	TACAAGATAAAACAG[-/G]AGCTTTTCTTTTTTT	8925
rs397813980	in-del	-/AT	0	0	intron-variant	HERC1	GRCh38.p7	15:63637403	TTGCTAGATAAAATC[-/AT]ATCAGGTTTTCACTT	8925
rs397815589	in-del	-/A	0.375	0.216506	intron-variant	HERC1	GRCh38.p7	15:63736625	GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAGAG	8925
rs397853980	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63625710	AAAAAAAAAAAAAAA[-/A]GAAAGAAATGGTATG	8925
rs397948490	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63768689	TTATGCCTTTCTACA[-/A]GTATGGAGAAAAATG	8925
rs397975072	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63698437	AAAAAAAAAAAAAAA[-/A]GGCTCTGATGACCTA	8925
rs398027616	in-del	-/A	0	0	intron-variant	HERC1	GRCh38.p7	15:63628968	GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAG	8925
rs398027617	in-del	-/T	0	0	intron-variant	HERC1	GRCh38.p7	15:63805960	ATTGGGTTTTGTTTG[-/T]TTTTTTTTTTTTGTT	8925
rs398039468	in-del	-/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63646512	GCCCAGCCTTCTTGG[-/T]TTTTTTTTTTTTTTA	8925
rs398043424	in-del	-/A	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63748976	CAAAAAAAAAAAAAA[-/A]TTCAAAAACCAACCA	8925
rs398043425	in-del	-/A	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63756270	AAGAATTAAAATTCA[-/A]TAATGTATACAAAGG	8925
rs398043426	in-del	-/A	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63760119	GGGGCAGAAAAAAAA[-/A]TTGAACTGGATAGGG	8925
rs527241214	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63738760	AGTATTCTTCTAAGA[C/T]GCAATGGCTGTCAAA	8925
rs527249589	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63788916	ATGAAAATGAGAAAG[C/T]ACATTAATAGGAGTT	8925
rs527277056	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63696013	TATCTTAAAAAATTT[A/C]AAGTCTTTGTATTTT	8925
rs527284067	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63741180	ATTACAGGCGTGCAC[C/G]TCCACACCTGGCTAA	8925
rs527291305	snp	A/G	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63711175	ATAAAAATTTAAAAA[A/G]TTAGCCAGAAATGGT	8925
rs527300327	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63808292	AACATCAACGTACTT[C/T]TTCTTTCCTCAAAGA	8925
rs527312300	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63702949	TCTCTACTAAAAATA[A/C]AAAAATTAGCTGGGC	8925
rs527351115	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63752012	GGTGTCTGTTATTTG[C/T]CTGTGTGTATACATC	8925
rs527353987	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63828539	AGATGGGGTTTCTCC[A/G]TGTTGGCCAGGCTGG	8925
rs527359079	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63652817	CACCACAACTGGATA[A/G]TTTTTGTATTTTTAG	8925
rs527367219	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63685605	TGAGATCTGTTGTAA[A/C]TGGCTAAGTCTAGGA	8925
rs527368806	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63742569	AGGGGGAAGGTTTTC[A/C]GTCTTTCTCCATTGA	8925
rs527372604	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63716675	ATATAGACACATATA[C/T]GCTCTTCCTTCCTCA	8925
rs527373012	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63745028	CCCTTCTGGCCTGGG[A/G]CATGTCTAGAAATGT	8925
rs527410006	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63659222	TCTTTTTATTGCTTC[A/G]GTATCATGAAAGACA	8925
rs527415054	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63795320	AAAAGAAGTTCAAAG[C/T]AGATAAAGAGTAGTG	8925
rs527439240	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63815519	TTACATAGTGACTGA[A/T]GAAGTCCTTTTCTAA	8925
rs527444650	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63657441	CCATTTGGAGATCCT[C/T]TTTTGTGAAACACTT	8925
rs527446500	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63674014	ACAGGCATGAGCCAC[C/T]ATGCTTGCCAGAATA	8925
rs527448060	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63682719	CTGCCACAATTTACC[G/T]TGTAAATGCTAAATT	8925
rs527469204	snp	G/T	0.000100013	0.00707083	missense	HERC1	GRCh38.p7	15:63775382	TGGCTGCTAAGAAGG[G/T]CATCCAAATAGTGGT	8925
rs527505219	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63767758	TGAAATGTCAATCAC[C/T]TTGGAGAGTTCTCCG	8925
rs527524977	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63724745	GGTACCAGATAAGTC[G/T]TCATGTTCAGTCTAG	8925
rs527532354	snp	C/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	HERC1, FBXL22	GRCh38.p7	15:63608374	AGTCAGAGAGACCCA[C/G]GATGACAGAAGAACA	8925
rs527554008	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63641105	TGATACCCGCATCCA[C/T]CCCTATCCCTCAACT	8925
rs527566327	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63828464	CCTGCCTCAGACTCT[C/T]GGGTAGCTGGGATTA	8925
rs527571538	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63731924	AGGAAATACGTGTAC[A/T]ATGTACAATTCTGGA	8925
rs527580886	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63631489	TGCCCTGGCTCATCA[C/G]TGACCTCTCTTCCCA	8925
rs527584840	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63640515	AATTAACCTACCGTA[A/G]TCTGAAAGTCTGGAA	8925
rs527585368	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63647386	TGAAAAGGGAACTCT[G/T]AAACACTGTTGGTTT	8925
rs527602706	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63822241	CATCATGTAGGACTT[C/T]GCAGGTCATGGCTAG	8925
rs527608583	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63739301	CTCAAAGGTTCAGGC[C/G]ATTCTCCTGCCTCAG	8925
rs527629873	snp	A/C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63782671	AAATACATTTTGTAA[A/C/G]GCTATAGCTGCCACA	8925
rs527643146	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63803400	CTTCTTATCAACATC[A/G]TGGTGTATATCATGC	8925
rs527677575	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63778040	GCATAGCTATCTGCC[A/C]AAAATTTAAGAAAAA	8925
rs527681504	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63762526	GACTAGGTTTCACCA[C/T]ATTGGCCAGGCTGGT	8925
rs527683838	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63703779	GCATAGTGGCATGTG[C/T]CTGCAGTCCCTCCCA	8925
rs527714214	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63753661	ATACATGCTGTTGTT[A/G]AAGACTATGGGGAAG	8925
rs527718491	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63620059	TGTGTTTGCTCTTGC[G/T]TCTCTAGTTCTTTTT	8925
rs527735799	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63627235	AGAAACAAAATCCCT[A/T]TGGGGAATCTTAGGA	8925
rs527736525	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63793003	ATACTTACATTTATG[A/G]GTTTATAATAAAGGC	8925
rs527741742	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63821163	GCATTAGCTCATGCC[C/T]ATAATCCCAGCACTT	8925
rs527742300	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63768366	ATGCCAGTGCTATTG[C/T]CTGTGGCTCACACTT	8925
rs527753095	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63717861	TGAGCGACAGAGCGA[C/G]ACTGTCTCAAAAATA	8925
rs527753120	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63619320	TTTTCGTATGTTGAA[C/T]CAGCCTTGCATCCCA	8925
rs527764320	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63816110	ATACCTAACATTTCC[A/C]AAAACTTGTTCCTCA	8925
rs527778991	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63651757	AACTATTAAAAATGC[A/G]GCTGGGCGTAGTGGC	8925
rs527780809	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63619207	GTTTTTAGCATGAAG[C/G]GTTGTTGAATTTTGT	8925
rs527798624	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63634136	AAAGTAAGTCAACAA[A/G]AAATAATTCTTAATG	8925
rs527813146	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63667012	CCCAAGCATAGTGCT[A/G]AAGTGCTGTCTAGTG	8925
rs527835102	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63740674	TTCCCTAATAATTAA[C/T]GATGTTGAACATTTT	8925
rs527867976	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63794492	AAGTACTAACCCTCT[-/A]ATCATGGCTCAGTCT	8925
rs527889015	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63784353	AACTAAAATGGAGCA[A/G]TCTCCAAGATACACT	8925
rs527889446	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63830428	AAAAATGTCAAGGTC[A/G]TGAAAAACAAAAACT	8925
rs527912436	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63697748	GAGTGAGCCACCGCG[C/T]CCGGCCAATCTTAAT	8925
rs527913921	in-del	-/AAT	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63622665	CAAGAGGATAACAAC[-/AAT]ATTTACTCCTTAGGG	8925
rs527921077	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63648814	TTTTTGAACCCTATG[A/G]AAGTATTACCTATTC	8925
rs527941356	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63756114	AGACCTTATCTGTCT[C/T]GTTCACTGCTACAAG	8925
rs527950707	snp	C/T	0.000636377	0.0178265	intron-variant	HERC1	GRCh38.p7	15:63754696	AACATTAACTCTTTT[C/T]CTCTAGGCCTTGACT	8925
rs527956325	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63648268	GACTTAAAAGACAGA[A/G]ACTTTGAAACAAATA	8925
rs527986543	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63796894	GAGAACAGATTGTAA[A/G]TGTTTCTTATCAGAC	8925
rs528002422	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63661182	ATAATAAAAACTGCT[A/G]GTATGTAGGTACACA	8925
rs528004205	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63769551	GTCCAAAAATAAAGT[A/C]GAAATTAAAATAAAT	8925
rs528007855	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63746160	TTTAATATAGATGTT[C/T]ATAAGCTATAAATTT	8925
rs528024333	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63797770	CCTGTCAGGAGATTA[C/T]AAAATGTTTACTGTA	8925
rs528027512	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63813390	GAGCCCATACATAGA[C/T]TACTCCAAAAGAGCC	8925
rs528035063	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63824888	TATATGTGGAATCTT[-/A]AAAAAAAAAAAAGTC	8925
rs528040148	snp	C/G			missense	HERC1	GRCh38.p7	15:63638442	AATGAGGGAGCTGCT[C/G]CAGGTACCATTACAT	8925
rs528098158	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63665521	GCCTGGCGACAGAGC[A/G]AGACTCCGTCTCAGA	8925
rs528104985	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63765483	TTATATCCATCCAGC[A/G]TTAACATCAATACTG	8925
rs528108106	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63757517	AACGATCCACCCGCC[C/T]TGGCCTCCCAAAGTG	8925
rs528126782	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63630289	ATAATACTTCTTTGG[C/T]CGCAGTCGAGAGAGA	8925
rs528147245	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63771978	AGAAACAAAATTAGC[G/T]GGGCATGGTGGCAGG	8925
rs528182095	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63720398	GGACTGCTAGTCTCC[A/G]TTCATTTGACAGATT	8925
rs528187637	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63629622	CACGGCACTGCCAGG[A/C]AACTCCCAAAGGTGC	8925
rs528204977	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63808138	ACAAAAAAAAAAAAA[C/T]ACATCACTACAATGT	8925
rs528211888	snp	A/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63812790	AAAAAATAAAAATAA[A/T]AAACGAAAAAATTAT	8925
rs528224276	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63678485	TCTTCATACATGTGA[A/G]TTATACCAACTGGCC	8925
rs528224331	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63670616	TCCTGGTGAATGCCT[A/G]TGGGAGCAAGGGGGC	8925
rs528246575	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63743311	TCTGTCACCAGGCTG[A/G]AGTGCAGTGGCACAA	8925
rs528274727	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63610498	GATATAAGGCAAGGG[C/T]TGTTTCCAGAGCTGA	8925
rs528282013	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63695721	TCCTCACAAAGCAGT[G/T]TTTCCTGCCTAAATA	8925
rs528305269	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63710026	TAGCAAAGGCTCAAG[A/C]GGTATGCTTGGGGTC	8925
rs528311467	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63610245	TATGGGAGGTGGATG[A/G]CCCAGCAGCCCAAAT	8925
rs528323262	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63832783	TCAAATAAAATAAAT[C/G]ATTTTTGGAACAAAT	8925
rs528344091	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63617003	GTTTTCTAAAATCAT[C/T]ATCTTTTTTTTTTTT	8925
rs528352156	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63707630	GTGTCAAAGAAGGCC[C/T]GGAAGTGACAAAACA	8925
rs528355630	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63726802	TTCAGTGAACAGGAA[C/T]AAAAGAAAGTTCCGC	8925
rs528355786	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63609825	CAATTAAACTCCAGT[C/G]CATCCATTCAACTGA	8925
rs528400133	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63757297	TGAGACAGAGTCTCG[C/T]TCTGTCACCTGGGCT	8925
rs528400702	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63657230	TTGTGGGTGTGCAAT[C/G]GTATCTCATTGGTGG	8925
rs528408928	snp	A/T	0.000167275	0.00914383	intron-variant	HERC1	GRCh38.p7	15:63664602	TATCAGGGCTACAAG[A/T]GCAAGTGAGAAAGCA	8925
rs528421499	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63800691	TATATATAATTTGTG[C/T]GATTTGTTTAATGTC	8925
rs528434379	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63680437	AGAGAAAGGAGAGAC[A/G]AGCAGATAATCTATA	8925
rs528437347	snp	C/T			missense	HERC1	GRCh38.p7	15:63775464	CTTTGAGGCATAAAA[C/T]TTGTTGGGGCAAAGG	8925
rs528469544	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63803985	AAATAGACCCACATA[C/T]ATATGGCCAACTGAT	8925
rs528471873	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63679597	TTTGGATGAGGTGAA[A/G]GAGAAAGTTTACAAT	8925
rs528487624	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63775992	GCAGTGAGCCGAGAT[C/T]GCGCCACTGCACTCC	8925
rs528511586	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63635033	CAATGCTTTTAAAAA[-/T]TTTTTTTTTTTAATT	8925
rs528512152	snp	C/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63631042	ACAGTGCAGTGGTGC[C/G]ACCTCGGCTCACTGC	8925
rs528541571	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63730600	GAAATGTAAATGTAG[A/G]CTATATATTAAATAA	8925
rs528552721	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63646052	AGAGACTTAAAAAAA[C/T]GCACCCCTTACATCC	8925
rs528574654	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63639021	TTCAAAGCTAGCCAT[A/G]TGTTTTCTGAACACC	8925
rs528579862	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63729902	TGGTGGTGGGTGCCT[A/G]TAATCCCAGCTACCG	8925
rs528597434	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63744010	GTTCTTGCAGCCTCA[C/T]AGAGGTACCACCTTG	8925
rs528612049	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63780397	ATCTAACAACAGGAA[A/G]TAAAGAAAGAAAACA	8925
rs528622985	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63757333	GCAGTGGTGCAATTT[G/T]GTTTCACTATAACCT	8925
rs528623886	snp	C/T	0.000157278	0.00886647	synonymous-codon	HERC1	GRCh38.p7	15:63694121	TAGATCCAACAAGGA[C/T]TGAACTACTTTGGGA	8925
rs528626847	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63686257	AATAGAACATTTACA[C/T]ATCACGATTTTTTTT	8925
rs528637454	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63658871	AATTTCTTAGGAGAA[A/G]CTCACATATTTCTAA	8925
rs528673153	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63618462	GCTTTGTTCTTTTGG[A/C]TTAGGATTGACTTGG	8925
rs528674062	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63767001	AGTTTTATAGGTTTT[C/T]CATTTGTTTTTTTTT	8925
rs528677873	snp	G/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63709181	TTTTTTATTTTTTTG[G/T]AAAGACAAGGTTTGG	8925
rs528689116	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63720397	GGGACTGCTAGTCTC[C/T]GTTCATTTGACAGAT	8925
rs528698066	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63752892	AATTTAAATACAAGT[A/G]TTACTTTTTAGTCAC	8925
rs528717587	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63774438	ATAAAGTTAGATGAA[C/T]TTCCCTAGTTCACAT	8925
rs528718089	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63708612	TTTAGCAAGCAGAGA[A/G]TAACAGTAGATAACA	8925
rs528736587	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63617656	CCTATTTCTCCACAT[C/T]CTCTCCAGCACCTGT	8925
rs528740222	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63766607	GCACATTAATAAAGC[G/T]TATCAACTATTAATG	8925
rs528761636	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63821532	CTGCACTCCAGCCTG[A/G]TAACAGAGTGAGACT	8925
rs528765408	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63723461	TGATAAACTTCAAAC[C/T]ATTTTAAGTAGATGC	8925
rs528796368	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63631666	CTGCCTCAGCGTCCC[A/G]AGTAGCTGGGATTAC	8925
rs528798459	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63814773	CACACACGGCCAACA[C/T]TAGCTTTCAAGATGC	8925
rs528823176	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63722951	CCTATAAATGTATTA[C/T]ATAAATCTCAATTTT	8925
rs528828105	in-del	-/TGTG			intron-variant	HERC1	GRCh38.p7	15:63691935	ACTGACTGTAATCTA[-/TGTG]TGTAAGCAGACATTT	8925
rs528840175	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63683530	GACTTTCTAGCCTAA[A/G]TACATATTTCTGAGT	8925
rs528852131	in-del	-/CAGT	0.174288	0.23826	intron-variant	HERC1	GRCh38.p7	15:63621611	TTGGTTCCATTCTCC[-/CAGT]CACTTTCAGGTACAC	8925
rs528919292	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63823492	ATTCTACCTAACTGG[A/T]AGAAGGAAGAAGGAG	8925
rs528924596	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63634386	GCTACCAGTGATGTT[A/G]CAATTCAGCCATACA	8925
rs528928580	snp	A/G	0	0	intron-variant	HERC1	GRCh38.p7	15:63642743	CTAAGCACTGTCACC[A/G]AAGTATGGGGTGTAG	8925
rs528933108	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63617448	AGTCTTTCCTATTAT[A/G]AATAGTGCCGCAATA	8925
rs528938325	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63648725	AAAAACAGTATCTGT[A/G]AGGGTAGAATGGGAG	8925
rs528945284	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63733207	AGAAAAGAACACAAA[A/G]GGATCCCAGAAAAAA	8925
rs528960119	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63829210	AATAACTTGAGCTCA[A/G]GAGCTCAAGGCCAAC	8925
rs528967903	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63740556	GCAATGCATGAAGGT[A/T]CTAATTTCTCCACCT	8925
rs528972512	in-del	-/AC	0.0115144	0.0749975	intron-variant	HERC1	GRCh38.p7	15:63792444	TACTGACTTTTCAAA[-/AC]CCTTTCCAGATACAA	8925
rs528994233	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63790974	AAGGCTTGTTTTTAC[A/G]AACATCATTTTAACA	8925
rs529002436	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63783313	AGCAACCCCCATCCC[C/G]ATCAGTCAGCAGCCA	8925
rs529004080	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63829934	GATCCCATAAGAACA[C/T]ACTAATATAAACAAA	8925
rs529008367	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63811028	TTAATGTCATTTGGG[A/G]AAAAAAAAGGCTGGG	8925
rs529021648	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63689216	AAAAAGGATACACTA[C/T]ATTTAGCAACAAACA	8925
rs529055613	snp	A/G	0.000284046	0.011914	intron-variant	HERC1	GRCh38.p7	15:63669735	TAGCATAAAAATCCA[A/G]TTTACGAAATAATAC	8925
rs529059210	snp	A/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63614837	GAAATAGAAAATGCA[A/T]TCTTCATTCAATTTC	8925
rs529062848	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63676427	CACTAAATTCTGAAA[C/G]AGTACCACTCCAAAA	8925
rs529080991	snp	C/T	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63621769	TGATACCCTTTCTTC[C/T]AGTTGATCGAATCGG	8925
rs529087724	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63668772	ACAGAGCTTTAAAAT[A/G]TATGAAACAGAAACT	8925
rs529095899	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63744398	ACAATCAGCCAGTGG[C/T]AAAGCCAGCCAGGCC	8925
rs529107255	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63739093	CAACCATCACCACTA[C/T]CCAATTTAGAATATC	8925
rs529118951	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63621255	CCTTCACTTATGAAG[C/T]TTAGTTTGGCTGGAT	8925
rs529129759	snp	G/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63763614	CAAGACTATAGTGTC[G/T]AAGGATGCACATCTG	8925
rs529130635	snp	A/C	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63769351	CTTGAACCTGGGAGG[A/C]GGGAGCTGCAGTGAG	8925
rs529162666	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63824207	ATGTAAATTGGAACC[A/G]CCATTATGGAAAACA	8925
rs529165884	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63810486	AAAATCTCTGGAAGA[C/T]ACATAAGAAACCAAT	8925
rs529204312	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63635355	CATCTGGCCAACTGG[C/T]ACATTTATCTGCCCA	8925
rs529215657	in-del	-/C	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63723556	AAAGGATGTGACACT[-/C]TACCAATTGTGACAC	8925
rs529216456	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63726224	TGACCTCAGGTGATC[A/C]GGCGGCCTCAGCCTC	8925
rs529218979	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63679993	TAATGGCAGAAGAAA[C/T]AGCTTATTATATTTA	8925
rs529244605	snp	G/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63791997	AGTTGGGGGCAAAGT[G/T]TAATAATTGATAACT	8925
rs529251015	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63691252	GGGCAGATCACTTAA[A/G]GCCAGGAGTTCAAGA	8925
rs529254468	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63729700	TGCTTGAAACTGAAA[A/G]TAACAACCTACCATA	8925
rs529261074	snp	A/G	4.35331e-05	0.00466526	intron-variant, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609289	GAGAGACCCAGAGCC[A/G]TGACTGGGGACATCA	8925
rs529292858	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63698035	TCATTTTAGCATTCA[A/G]CAGTGGGTCTTGATT	8925
rs529300073	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63792745	AGCAATCTTGCAGCA[C/G]ACGCTAGCTGGGTGT	8925
rs529307436	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63705344	TTTTTGGCAGAGACA[C/G]GGGTCTCACTATGTT	8925
rs529356013	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63615322	GAATATAAATACAAA[C/G]GAATCACCAAGTGCG	8925
rs529364996	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63717045	AAGAAAAGAATCCTT[A/G]AAACAGATACTCAGA	8925
rs529373836	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63805094	TTTGCCCAGAAAAAT[A/G]AGAATACATGATTAC	8925
rs529389544	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63671997	AATTTACAAACCTAT[C/T]AAAATAGAGTTGGCT	8925
rs529410377	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63756122	TCTGTCTTGTTCACT[C/G]CTACAAGTCTAATGC	8925
rs529413220	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63700339	AGGGAAGTATCTTAA[A/G]GTACCCAATTAAATA	8925
rs529422218	snp	C/G	0.00619381	0.0553041	intron-variant	HERC1	GRCh38.p7	15:63723401	ACATCATAAATTTTG[C/G]TGCTACAGATAAAAT	8925
rs529424105	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63662139	AATATTTCCAACATG[C/T]TCATTAATGCTAAAT	8925
rs529436012	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63764330	AACCAAATCCTAACA[C/T]TAGGTCATGAAACTA	8925
rs529476610	snp	C/T	1.71793e-05	0.00293076	intron-variant	HERC1	GRCh38.p7	15:63677839	GTGTAACTCAACAGA[C/T]CATACCTGATAGTAA	8925
rs529495690	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63778732	CACAAAAACGAACAT[G/T]AGAAAACTCAAGTGC	8925
rs529507585	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63831129	ATTTTGCTTTTGAGA[C/T]AGAGTCTCACTGTGT	8925
rs529533610	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63779455	ATAAAGCAAAAACTA[C/T]AGGAGATGCAAGGAA	8925
rs529534519	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63825652	TAGCAGCAAAGGTGA[C/T]TGTACTTTAAGACTA	8925
rs529543372	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63831836	TTTATATTAATAAGC[A/G]GATTAAGTGACGCAT	8925
rs529584007	snp	A/G	2.27788e-05	0.00337474	missense	HERC1	GRCh38.p7	15:63643505	GAGTGATGTGTCCCC[A/G]CAGCTGATAAACACA	8925
rs529594105	snp	C/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63816590	AGCTATTTATTTCAT[C/G]ATGAGATTTTAACCT	8925
rs529635090	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63691636	ATAAGCCTTACCTTA[C/T]TAAAGGAAAAAAAAA	8925
rs529635765	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63649670	AATGCCAAAAAGCTA[A/G]GTCTAGAAAGGAAGT	8925
rs529636769	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63612171	CCAGCCTGGGCCACA[C/G]AGTGAGACCCTGTCT	8925
rs529647478	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63688655	ACCTATAAAGGAGAA[A/T]GAGAACAGGCCATTC	8925
rs529650627	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63702517	CATCTTCAGCTTAAA[C/T]ATGAAAACTAAAATC	8925
rs529650903	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63611651	GAAGAGGCAGTATGA[C/T]GATCCTTCTGCCAAG	8925
rs529659338	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63717200	GATACAGAGTAGTCA[A/G]ACTCACACAGTACAT	8925
rs529671496	snp	A/G	0.000798403	0.0199641	utr-variant-5-prime	HERC1	GRCh38.p7	15:63833946	CTTGTCAAAGGGAAA[A/G]ACGTAAGAGGCGGCG	8925
rs529686191	snp	A/G	1.66613e-05	0.00288623	missense	HERC1	GRCh38.p7	15:63694417	TGCAGGGGCTGTCCT[A/G]GCATGGTGTCTGTAC	8925
rs529715482	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63788011	AAAAAACCTTACAAG[A/C]CAGTTTCATCAAATT	8925
rs529725155	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63617636	ACCAACAGTGTAAAA[G/T]TGTTCCTATTTCTCC	8925
rs529778851	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63759568	TTATTGTTAGCAAAA[C/G]TAAAGTTTTTCCATC	8925
rs529789259	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63665393	AAAAAATGAGCCGGG[C/T]ATGGTGGCACATGCC	8925
rs529817383	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63760210	CAAACTGGAAAACGA[A/C]TTTTTTTTAACATTA	8925
rs529840641	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63784302	AGACCACAGTTCTAG[C/T]CAGAAAGTAGTGAAA	8925
rs529853726	in-del	-/A	0.205687	0.246041	intron-variant	HERC1	GRCh38.p7	15:63659237	GTATCATGAAAGACA[-/A]AAAAAAAATCAAAAC	8925
rs529873624	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63635290	CTGGCCTCAAGCAAT[C/G]CTCTTGCCTTGGCCT	8925
rs529881562	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63688258	GAGATTGTATGGATA[C/G]AGAAATGGGGGTGAG	8925
rs529888935	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63731368	CACATCAGAAAGAGA[A/C]AATAATTTATTATTT	8925
rs529890176	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63789385	GTGAGCCACCGCGCC[C/T]GGCCAAAAGGTTTTT	8925
rs529896414	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63681360	GTGTACACCATCATG[C/T]CTGGCTAGTTATTTT	8925
rs529902698	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63695293	CCAACAGCCTTGGCC[A/T]CCCAAAGTGCTGGGA	8925
rs529904907	snp	A/T	0.00953873	0.0683987	intron-variant	HERC1	GRCh38.p7	15:63613613	TTTTTACTATCTATA[A/T]GCATATCCTATATTA	8925
rs529916165	snp	A/T	0.000347396	0.0131749	intron-variant	HERC1	GRCh38.p7	15:63774669	AACTATTATGAACTT[A/T]AAAGTTGAGACTTAT	8925
rs529931337	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63646853	AAACAAAACAAAACA[A/G]GAAAAAGCAACTATC	8925
rs529935031	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63687470	TTGAACCGGGGAGGC[A/G]GAGGTTGCAGTAAGC	8925
rs529936786	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63821866	AAACAACATATCCAA[A/G]GTTCCTGCTTTCATG	8925
rs529942228	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834996	ACGGTATAGACAGAC[A/G]AGGGAGTGCTTTCCC	8925
rs529966871	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63744978	AGGTGATGAATGCTG[C/T]CAGTACTGAGTCCTT	8925
rs530013610	snp	A/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63666903	CATGTTTCAGCTCTC[A/T]TGTGAAAAACAAGTG	8925
rs530021848	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63619259	TTGAGATAATCATGT[A/G]GTCTTTATCTTTGGT	8925
rs530023366	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63646222	GCCTAGATGGTCCTG[A/T]AAATATCTGAACTGG	8925
rs530035007	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63767661	CGAGATCGCCCCACC[A/G]CACTCCAGCCTGGGA	8925
rs530035883	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63652719	GTGCAGTGGCTCAAT[C/T]TCAGCTCACTGCAAC	8925
rs530066636	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63808813	GAATGAAGATCCTGA[G/T]GGTCCTTATCATATT	8925
rs530073287	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63717290	CATTTCATGGACTTT[A/C]AAGGTCACCAACAAA	8925
rs530079131	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63626642	AACATATAGGTGCAT[A/G]ATTCATGAGGCTTTT	8925
rs530094016	snp	C/T	0.000399281	0.0141238	missense	HERC1	GRCh38.p7	15:63775310	AGTACAAGCAGTCGT[C/T]TTCTAAGTGCCCCGG	8925
rs530114199	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63709835	AATACATAAATAAGT[A/C]CAACATAAGACAAAC	8925
rs530116321	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63821710	CCAGCCTGGGAGACA[C/G]AGTGATACCCTGTCT	8925
rs530143629	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63731828	GTGTAGCTATATGCA[C/T]CTCTGGCTAGATGGG	8925
rs530146762	in-del	-/A	0.230896	0.249269	intron-variant	HERC1	GRCh38.p7	15:63698420	CGAAACTCCGTCTCC[-/A]AAAAAAAAAAAAAAA	8925
rs530151578	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63632167	TCAGAGGCATCGATG[G/T]TCTCCCACAACTAGA	8925
rs530168562	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63795037	TGCCACTGCATTCCA[A/G]CCCGGGCAACAGAGC	8925
rs530195693	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63814870	AATTGTTAAGAGGAT[A/C]AAATAAGAATTCATA	8925
rs530214026	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63697093	AAGACATTAACATTG[C/G]TACAATACTATCAAC	8925
rs530224172	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63723716	AAAAACCAACGCGTT[A/C]AAAATGGAATGATAT	8925
rs530230868	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63815365	TTGCTATGTCACTAA[C/T]TCTGCAATGTAACCT	8925
rs530295951	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63762436	TCAAGCAATTCTCCT[A/G]CCTCAGCCTCCTGAG	8925
rs530304594	in-del	-/TAA	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63685383	TGATTACAGGTGCCC[-/TAA]TAATTATAAATTCTT	8925
rs530312155	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63714416	CACCAGGAATACCCA[C/T]CTGATGCCAGCCTTT	8925
rs530317187	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63797673	GCATGGCATGGCCAG[C/G]CTCCTGTCAATTAAA	8925
rs530319385	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63613585	TATGTTAATTTGCTT[A/C]ACTATAATAACCTTT	8925
rs530363123	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63660136	CCAGCCTGGCCAACA[C/T]GATGAAACCCCATCC	8925
rs530369575	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63741553	TTCAGGTGATCCACC[C/T]GCCTCGGCATTCCAA	8925
rs530372878	snp	C/G			missense	HERC1	GRCh38.p7	15:63775076	AGACTGAGACCAGGT[C/G]CTGACACAGGCATCA	8925
rs530374502	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63703239	CAGACCAAGGGCTTA[C/G]ACCAATTGTGAAACA	8925
rs530374774	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63710724	AGCACAGGCTTCATG[C/G]AAAAAGTAACATCAG	8925
rs530386227	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63619977	TTTTTTGAAGGTTTT[C/T]TGTGTCTCTATCTCC	8925
rs530391582	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63610841	GAACTGCCCAGCTCA[A/T]GTGGGAGAGAGGGCT	8925
rs530405995	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63809611	TGAGAAATATGGGCC[G/T]AAAATAAAAGAGGAA	8925
rs530413960	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63771055	TTAGCCAGGCATGAT[A/G]GCAAGTGCCTGTAAA	8925
rs530421498	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63660681	ACTTTCCACAATTAG[A/G]GTGGAAATTCAAAAT	8925
rs530436787	snp	C/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63669820	AGTTATAGTTTAATG[C/G]AGGGTGGGGAGAAAG	8925
rs530449704	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63764260	TAAAATTAGTTAAAC[A/C]GTCTACAAAAACAAC	8925
rs530452989	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63641114	CATCCATCCCTATCC[C/G]TCAACTTTGGAATGG	8925
rs530455865	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63667685	ACTACATATGAAGTG[C/G]TACAATATCACCTTA	8925
rs530467532	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63629597	TCAACATCATTAGGA[A/G]GGATCACGTCACGGC	8925
rs530479839	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63637289	CAAAAAGTGTTATTT[A/C]TATTTCACTGAATTC	8925
rs530481066	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63811758	AGCTTGCAGTGAGCC[A/G]AGATCGCGCCACTGT	8925
rs530493349	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63644206	GACAACATAATACTA[C/T]ATGTATTCACTACCC	8925
rs530496240	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63786863	TAAATGCCACTAAAT[C/T]GCTCACTTTAAGATG	8925
rs530500167	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63670516	TCTACTAAATGATGT[A/T]CGCCCAGTAAGAGCC	8925
rs530510428	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63622358	TTTGAGATGTGGTCT[C/T]GCTCTGTTGCCCAGG	8925
rs530518241	snp	C/G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63811387	TGCACCAAAATGTTG[C/G/T]AATTTGTGAATCTAG	8925
rs530527203	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63643970	TCCTCTTTTTGTTGG[C/T]TAATGGTTCTGTCTG	8925
rs530583410	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63778581	TCCTGCAAGGCAAAA[C/T]AGACCCATAAAATTG	8925
rs530606514	snp	C/G	0.000116744	0.00763925	synonymous-codon	HERC1	GRCh38.p7	15:63727735	AGGTGGCAACAAGTC[C/G]AGGAGGTAACTCAAT	8925
rs530607920	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63817917	AGAAAAAATGCTGTA[C/T]GGGAATTGAATTATC	8925
rs530644237	snp	A/C	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63655210	AATAGAAAAATTAGC[A/C]GGGCATGGTGGCATG	8925
rs530645303	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63818407	GGAGCCAAACCGACA[C/G]ATGGCAGACGAAAAG	8925
rs530647909	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63699088	GCTGCTACCATAACC[A/C]ACTGGTGAAAAATGG	8925
rs530655515	in-del	-/TTTAT	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63765860	CTTGGCAAAATAAAC[-/TTTAT]TTTATTTTTTTGAGA	8925
rs530672747	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63684940	CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG	8925
rs530678668	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63686978	GCAACAGAGTTCAGT[A/G]ATTTAAAGACAAGCA	8925
rs530689067	snp	C/T	4.18524e-05	0.00457432	intron-variant	HERC1	GRCh38.p7	15:63622798	GACATATAATGAACA[C/T]TTGCTGACTGCCATA	8925
rs530693764	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63700821	TTCTTTCATGTGACA[C/T]AGAAAAAACTGAAAA	8925
rs530695601	snp	A/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63799944	GCCTGAGCCTGCGCA[A/T]CAGTGTGAGACTCCA	8925
rs530736096	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63609412	GAGACTGGGCCAGAT[A/G]GAATGAGCTGAGGCC	8925
rs530740922	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63799333	TGGCAAAACCCTGTC[C/T]CTCCAAAAATTAAAA	8925
rs530757232	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63707051	CACTAACTAAAAAAC[G/T]CACATTAATTAACAT	8925
rs530788444	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63779687	AATGTATAAATGTTC[C/T]GATGACTGGTAAGGC	8925
rs530798992	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63686157	AACATTTTTGAGATA[A/C]CTTTAGAATTATAAG	8925
rs530817856	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63780936	TGTATATAACTATAA[A/G]TCTAATAAGTAAATC	8925
rs530821363	in-del	-/T	0.00636936	0.0560724	intron-variant	HERC1	GRCh38.p7	15:63670177	TATGGAAAGAAAAGG[-/T]TAACTGTCTAGTCAC	8925
rs530828077	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63693190	CTCAACAACAACAAA[A/G]AAAACCCAGAAAACA	8925
rs530834723	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63685649	TAACTGAAGTCAATA[C/T]TACTGGCCAATCTTA	8925
rs530835264	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63757486	TGGTCAAGCTAGTCT[C/T]GAACTCATGATCTCA	8925
rs530854249	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63645423	AAGCCACACTTAATG[A/C]AGATAACAGTCTATA	8925
rs530862194	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63700368	TATGCATAAAAATTA[C/T]ATCAGTTATGTAACT	8925
rs530870592	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63805892	AAGCTGCAGCAAGCC[A/G]TGATCATGCCACTGC	8925
rs530890807	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63651150	TGTTGGAAGGCTTGT[C/G]AATTTCAAGGTGAAG	8925
rs530906009	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63815943	CCCTTTTAAAACCAT[C/G]AGATCTCATGAGAAC	8925
rs530908627	in-del	-/A	0.0011988	0.0244533	intron-variant	HERC1	GRCh38.p7	15:63818143	TTATAGCTCTCTGTG[-/A]AAAAAAGTGTTTAAG	8925
rs530936167	snp	C/T	3.02641e-05	0.00388987	intron-variant	HERC1	GRCh38.p7	15:63749610	ATTTACACAAGACAA[C/T]AGTTAATACTATTTC	8925
rs530947411	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63780254	TTTTGATTTTGTGAT[C/T]ACTATGAATGGAATT	8925
rs530970415	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63814070	ATCTCAAAAAACAAA[A/C]AACAAACAACAACAA	8925
rs530973615	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63826264	GGTTTTTTGGCACCG[C/T]TAAAATCTAATAGGA	8925
rs530975089	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63736798	TTTTAGTAGAGATGG[A/G]GTTTCACCATGTTGG	8925
rs530986310	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63672489	CATTAAAGGTCAACT[G/T]CTCTACCTGAGAAGA	8925
rs530987962	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63692675	ATCTAATGCAAAATC[C/T]TAGGCTGTCAGCTAC	8925
rs531004733	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63707723	CGCTTGAGGCCAGGA[A/G]TTCGAGACCAGCCGG	8925
rs531017224	snp	C/T	1.65663e-05	0.002878	intron-variant	HERC1	GRCh38.p7	15:63644988	AAAAACACCAGAATG[C/T]TACCTGGCAATTTGA	8925
rs531030195	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63832685	TTTGGAAAAGGGCCC[A/G]GTGAAAAAGATAGTG	8925
rs531053951	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63650465	GTTGCCCAGGTTGGA[C/G]TGAGTACAATGGCAT	8925
rs531073256	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63753429	ACAGGTACTATATGC[A/G]TATAATTTTTCATAA	8925
rs531083952	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63730372	GCTGAGGTGGGAGGA[C/T]CACTTGAGCCCAGGA	8925
rs531086424	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63820346	ATATTACTGACTAAA[A/T]TTCATTATACATGAC	8925
rs531104442	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63668315	TGGGCAACATGGTAC[A/G]ACCCTGTCTCTACAA	8925
rs531120930	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63765730	CCAATAAGATCTTAC[A/C]TGTACTGATTGATAT	8925
rs531141038	in-del	-/A	0.000696795	0.0186524	intron-variant	HERC1	GRCh38.p7	15:63729482	ATCACCATAAAAGAC[-/A]AAATAATCGCATACC	8925
rs531148608	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63726257	AAAGTGCTGGGATTA[C/T]AGGCATGAGCCATCA	8925
rs531154864	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63766553	CACTGCACTCCAGCC[C/T]AGGTGACAGAATGAG	8925
rs531159237	snp	C/T	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63758737	TTCCAGAATTGTTCA[C/T]ATACAAATTATTTAA	8925
rs531174216	snp	A/G	0.00636936	0.0560724	intron-variant	HERC1	GRCh38.p7	15:63631570	TTGAGATGAAGTTTC[A/G]CTCTTGTCGCCCAGG	8925
rs531185033	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63630927	CTTCTCCAATATCCA[C/T]ATCTTTGAAAGGATA	8925
rs531193600	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63689136	GAATATACGGAGATC[C/T]GGGAGAAAGCGTTTT	8925
rs531208832	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63722222	CCACCACAAACTTGC[A/G]TAGTACTTTACCATG	8925
rs531229402	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63688565	TAAGAAATGGGCATA[C/T]GAGTCTGAATAAGGT	8925
rs531249876	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63638994	CTATCACTATCACTA[C/T]GGCATTGGTGATTCA	8925
rs531258355	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63629858	GGAGCTAAAAGTCAC[C/T]GTCATAGCATCTCAG	8925
rs531262356	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63752932	TGAAATACTCTAAGT[C/G]TTTTATACTCATCCC	8925
rs531287275	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63647430	TACAAACTCTATAGA[A/G]AACAGTATGGGGATT	8925
rs531301609	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63665512	TGCACTCCAGCCTGG[C/T]GACAGAGCGAGACTC	8925
rs531302347	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63742726	ATCCAGATAATCACA[C/T]TGTTTTTGTTCATTT	8925
rs531317081	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63782687	GCTATAGCTGCCACA[A/G]ATAGTGATTCCTCTG	8925
rs531321443	snp	A/C	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63682383	AGAAAGGGCCCAAAT[A/C]TTCCCACAAGTGGGC	8925
rs531323908	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63653415	ACCACTGTACTTCAG[A/T]CTGGGTGAGACTCCG	8925
rs531348969	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63769181	CCAGCACTTTGGGAG[C/G]CCTATGCAGGTGGAT	8925
rs531387307	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63620402	ATTTGCTGAGGAGTG[C/T]TTTACTTCCAACTAT	8925
rs531407043	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835184	AGTTCCTTATGTGTC[A/G]ATTTATAATGCCAGT	8925
rs531415921	snp	A/G	0.00157649	0.0280314	missense	HERC1	GRCh38.p7	15:63675040	AGGCCTCGGAATCGC[A/G]CCACATCAAACGGCA	8925
rs531419191	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63710747	AACATCAGAATGAAG[A/G]CTTGAAGAAAGAGAG	8925
rs531422875	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63739346	AGGACTACAAGCACA[C/T]GCCACAACGCCAGGC	8925
rs531444610	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63717949	AGAAAGCCTATTTTC[C/G]TAACATTCAGCTAAA	8925
rs531452327	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63627314	GCTCTTAGGCACAAT[A/G]TTGCTTCAGGGAAAT	8925
rs531460050	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63745595	TCCCCAAGCACCCAG[A/G]GACACTCTCTGCACC	8925
rs531481261	snp	A/G	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63739251	TGCCCAGGCTGGAGT[A/G]CAGTGGCGTGATCTC	8925
rs531482851	snp	A/G	1.65715e-05	0.00287845	missense	HERC1	GRCh38.p7	15:63725369	GTGTCCTGTTCCTCT[A/G]GAGACACAGGGGAGC	8925
rs531494210	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63809815	AAAAAAGTAATAAAA[C/G]CAATGAAAAGGGGAA	8925
rs531506288	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63675608	AGTTTATAAATGGTT[A/G]CTTATAACTTATTTC	8925
rs531516822	snp	G/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63628009	ATGGTTAACTAAGGT[G/T]AGGAATTTGACAAAT	8925
rs531520275	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63732349	ATTCTTTAATATAAA[A/G]AAGTTATTTAATACA	8925
rs531522802	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63776729	CTAACATTCAGGGAC[A/G]CCAAGGCAGGAGGAC	8925
rs531523226	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63816157	AGATGTTATAAGGAG[C/G]AAAAAAGGTTCAGAG	8925
rs531525128	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63823381	AAGATTTTGTTTATT[A/T]CATCCTCACATCAGC	8925
rs531548900	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63682966	CATGGTGAAACCTTA[C/T]ATCTACTAAAAACAC	8925
rs531561673	snp	C/T	1.65652e-05	0.0028779	missense	HERC1	GRCh38.p7	15:63674921	CATCCCCTTTCTCCT[C/T]GGATTCATGTCGGTG	8925
rs531562433	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63762568	GACCTCAGGTAATCC[A/G]CCCACCTCGGCCTCC	8925
rs531564669	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63769215	CTGAGGTCAGGAGTT[A/C]AAAACCAGCCTGGCC	8925
rs531574112	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63726136	ATAGGTGTGCACCAC[A/G]GTGCCTGGCTAATTT	8925
rs531595180	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63634241	AGAGGAAAAGTATAC[A/G]TGACCCAAAAATATT	8925
rs531597637	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	HERC1, FBXL22	GRCh38.p7	15:63608211	CGTGCTCATTTTGTC[C/T]TTGTAGGTTCTTCAT	8925
rs531638136	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63704864	CTGCCTCAGCCTCCC[A/G]AATAGCCAGGACTAC	8925
rs531641995	snp	G/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63641896	TTTTTAAGGAAAAAA[G/T]GTCAATAATTAACTA	8925
rs531660802	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63711455	TATGAAGTGGAAGCA[C/T]AGAGATATTAATGCA	8925
rs531665121	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63613676	ATTTATTATATATAT[A/T]AAAAAAAACTGGGCC	8925
rs531689349	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63698019	TTCAAGTTTTGCTCA[C/T]TCATTTTAGCATTCA	8925
rs531696665	snp	C/T	2.65805e-05	0.00364549	synonymous-codon	HERC1	GRCh38.p7	15:63718688	TAAGTGTTTACCAGG[C/T]TGATATCTAAATGAA	8925
rs531696719	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63710867	AGCTAAGAGTCCAGT[A/G]TGACAGAAGGAGAAT	8925
rs531711937	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63754823	ATCTTCCAAGGTGCT[C/T]CTAAACTGGGTCATA	8925
rs531748392	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63803905	AGTAATCAAGACGTG[A/G]TAGTGGCAACAAGAT	8925
rs531760203	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63731649	TTAGTGATCAGCCTT[C/T]CAATGTGGGCGGGAT	8925
rs531769212	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63755511	CAAGTAAGTGCTGAA[A/G]TACATGCCTGTAATC	8925
rs531784331	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63818651	TAGCTTTGAGAGTTT[C/T]GAAAAATCCTTCTTA	8925
rs531793332	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63785040	TTATCTAGAAAGTTA[C/T]ATAAAAGAAACATAT	8925
rs531794337	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63768244	AGGATGTTGCTTCTC[A/T]AATTTCAATGTTGAC	8925
rs531800706	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63621148	AGTTCTTCCTTTCCA[C/T]GTTTAGTGCTTCCTT	8925
rs531804097	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63763032	TCTCACCACCTATTT[C/G]TTTGTTGGATTACCA	8925
rs531809953	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63780941	ATAACTATAAATCTA[A/G]TAAGTAAATCATTTT	8925
rs531822699	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63614731	ACCATTTTTGGACAC[C/G]ATATTTATGACCACA	8925
rs531829782	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63777842	TTGAGAGATTTTTTT[A/T]AAAAACCTGAGTCTT	8925
rs531838921	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63661224	AATCAATGATTATTT[G/T]ACCAAACTACTGGGG	8925
rs531842422	in-del	-/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63791776	AAAATTTAGAATGAA[-/T]TTTTTTCCTTACTAA	8925
rs531846540	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63801887	TAATGAATCCAGTCA[A/G]AACTTCTCCTGAGCT	8925
rs531854662	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63659187	CACCAAGTTTTTTTT[A/T]AAATAACAAGTTCTA	8925
rs531864848	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63642874	CATCAGGTTTCTCCT[C/G]CATAAAGTGGGGTGG	8925
rs531876191	snp	A/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63660849	TTTTTAAGGGAAAAT[A/T]TAAGTTAACATGTAC	8925
rs531906416	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63740829	CTAGAAACTAGAACC[C/T]CATCAGATCTATGAC	8925
rs531932014	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63648885	ATGTAAGCAGGCACT[A/G]TGACTTTGAATTACC	8925
rs531950041	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63785857	CAACAGGATTGATAT[C/T]TCAGAGAGATTATTC	8925
rs531971933	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63750705	GGGAGGCTATGGCAG[A/G]AGGATCACCCAAGCT	8925
rs531973049	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63615993	TTTTACATACAAATA[C/T]GGCACAGCAATAACA	8925
rs531975677	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63610600	TGGCAAGTCATGCAG[A/C]AAATTTATGGAAAGG	8925
rs531976280	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63643299	TTCCTCAGTATTCAA[A/G]AGATTACTATATAAA	8925
rs532014932	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63750278	GCAATAATTATCACT[C/T]ACAAAGAGGGCCATG	8925
rs532046315	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63759417	AGGCTGCCTGCCAAA[A/C]GCATAGGACCCAGAG	8925
rs532051360	snp	A/G	0.000399281	0.0141238	synonymous-codon	HERC1	GRCh38.p7	15:63616469	CCCACTGTCTTCAAT[A/G]TGAAGAATGCTGTTG	8925
rs532055950	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63747302	CCGCCTCTACTAAAA[A/T]TACAAAAATTAGCTG	8925
rs532064565	snp	C/G			upstream-variant-2KB	HERC1	GRCh38.p7	15:63834123	CGAAAAGGGGAAAGG[C/G]ATTTGGGAGCGAGGG	8925
rs532065249	snp	C/T	0.000399281	0.0141238	missense	HERC1	GRCh38.p7	15:63655792	CTTAGTTTGGCCCCT[C/T]TGTCTGCTAGCAATG	8925
rs532097361	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63708696	GTAGTTAACTTCTAA[A/C]ATTTTAAAAAGCATT	8925
rs532099027	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63665122	GATATTCTATACATC[C/T]CATTTTAGGATAGGC	8925
rs532122128	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63700670	GCTTAATTTTCACCA[C/G]TGCACTCCAGCCTGG	8925
rs532132562	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63758429	AGTCTGGGCATTTTT[A/T]ATACATATCCTCTGA	8925
rs532151069	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63801058	AAAGCTTTCAGGTTG[A/G]TGAACACATCAAGAT	8925
rs532151245	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63794001	ACTCACCAAAACTGC[A/G]ATGGCCATGAGAGTG	8925
rs532158835	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63707650	GTGACAAAACAAGGC[C/T]GGGAGTGGTGGCTCA	8925
rs532184964	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63808644	GAGTAAAGTAAGTTA[C/T]CCACTTGTCAAGTTC	8925
rs532257034	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63701426	ATTAAATCTTCTGCA[A/G]TTTAAAGCAGGGGTT	8925
rs532266449	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63806552	GACTCATGCTTTGCA[A/C]GGCTGGTACTCTGCC	8925
rs532275217	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63664061	CTAGCAGTGAAGCCC[C/T]AACAACCACAGAGCA	8925
rs532287117	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63737710	TATTGAAGGTTATGA[A/C]TTTCCCCACATCAGT	8925
rs532300110	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63743387	CTGCCTTAGCCTCCC[A/G]AGTAGCTGGGACTAC	8925
rs532310070	in-del	-/AAAT	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63825302	AGACTCTGTCTCAAA[-/AAAT]AAATAAAGTTAGCAA	8925
rs532312464	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63787890	CGCCTGAGTCCAGAA[A/G]GTCAAGGCTGCAGTG	8925
rs532359489	snp	A/C	3.1793e-05	0.00398691	intron-variant	HERC1	GRCh38.p7	15:63694275	TGGAGGAAGACCAGA[A/C]TTCATACAGTTCTAC	8925
rs532363128	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63774567	CTCCAAGTATATGAA[A/G]TATTTAATTAACTCA	8925
rs532375976	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63673416	ACAAGAAGAAAAGGA[A/G]TAAGTACAAAGGAAA	8925
rs532386086	snp	A/G	8.36855e-05	0.00646806	intron-variant	HERC1	GRCh38.p7	15:63625901	CAAAGGCAGAGGGAA[A/G]GGCCCTGGGGCCTGG	8925
rs532400029	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63754147	TCACTGCACTCTAGC[C/G]TGGGTAACAAAGCAA	8925
rs532423042	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63773893	TTGGTTTTCACAAAG[A/G]TATATTTCAGTCTTA	8925
rs532443227	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63615262	AACCGATTTAAGGCA[C/G]TGGGTATGGAGAAAA	8925
rs532444130	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime	HERC1	GRCh38.p7	15:63833861	GGTGGGGCGCGGCTC[C/G]GGCGACCCGAGCCCG	8925
rs532456111	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63651688	GACATTGATTCTTAT[C/T]TGCCTAAACTCTTGG	8925
rs532476670	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63731284	AATATGAGAACACTG[C/T]AGGGCCCTTGCTCTA	8925
rs532484007	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63738577	TTTTAAAGAAGAAAA[C/T]TCAGAGAGGGTCAAA	8925
rs532487085	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63827720	AGCATTATTCATAAC[A/T]GCTAAGAAGTAGAAA	8925
rs532492566	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63794461	TCCCCTTCCCAGAGG[C/T]TGGGGATGGGGCTGA	8925
rs532522425	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63660110	GATCACATGAGGTCA[C/G]GAATTTGAGACCAGC	8925
rs532539258	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63674313	CTCAACAGCACAAAA[G/T]CAAAAAAAAAAAAAA	8925
rs532547662	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63827326	ACTTGGGTGGCTGAT[A/G]AAGGAGGATCGCTTA	8925
rs532564445	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63802417	AACCTGGAAACAGAC[A/G]TGCCTATTCGGTGAG	8925
rs532584190	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63624942	ATTTCCTTCCAGTTC[G/T]CTTCTGTGTATGCAC	8925
rs532586955	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63804066	ACAAAAGGTGCTGGA[C/T]CAACTGAATATGCAA	8925
rs532588652	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63723639	CCCTACAACTCTGGC[A/G]TTTTGGCAGGCAGAG	8925
rs532598268	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63631694	TACAGGCGCCTGCCA[C/T]CACGCTCGGCTAATT	8925
rs532610836	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63775834	CTTGAGGCCAGGAGT[C/T]CAAGACGAGCCTGGC	8925
rs532627546	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63767620	GGAGAATCACTTGAA[C/T]CCAGGAGGCGGAGGC	8925
rs532657948	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63666764	AATAAAATTTATTTG[C/T]AATCTCAAAATCAAT	8925
rs532658180	snp	C/G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63659528	AAAGTGCTGGGATTA[C/G/T]GAGCATAAGCCACCA	8925
rs532674795	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63659623	TTGTTGGGGTGAGAT[A/G]ATGTTGAACCATTAG	8925
rs532698572	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63738902	ATAAATATTAAATCA[A/T]CACAGTTCCTACTCA	8925
rs532728234	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63808672	TTCAACAGTCTGTTA[C/T]GGTAATAGATACAAT	8925
rs532742157	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63748205	CACTCCAGCCTGGGC[A/G]ACAGAGTGAGACTCC	8925
rs532751558	snp	A/G	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63817778	GATAGAAATATAGAT[A/G]AAACAAGACTGCCTA	8925
rs532765491	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63801646	TATTTCCTGAATTAA[A/G]CTAAGCAATCTGAAT	8925
rs532768529	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63702594	CATAGCAAATCTTTT[A/G]AGTTTTATCAAAGTA	8925
rs532768760	snp	C/G	0.00716266	0.059414	intron-variant	HERC1	GRCh38.p7	15:63825606	GGCTTATTTTGTAAT[C/G]AGTAAAATGAAGTAT	8925
rs532793367	snp	A/C	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63675979	TGCGATCTCAGCTCA[A/C]TGCAACCTCTGACTA	8925
rs532815758	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63613617	TACTATCTATATGCA[C/T]ATCCTATATTATCGT	8925
rs532817263	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63717201	ATACAGAGTAGTCAG[A/G]CTCACACAGTACATG	8925
rs532828207	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63643198	CCAATCACATACCTA[C/T]TACAAAATTTTCTAG	8925
rs532829246	snp	C/T	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63618555	AAAGTCATTGGTAGC[C/T]TGATGGGGATGGCAT	8925
rs532837021	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63808099	TTATGGAAGTTTAGC[A/G]TAACATTATAGTAAT	8925
rs532851685	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63815226	CCTCCAAAAAGACTT[C/T]AAATCCCCTCTTAAT	8925
rs532855900	snp	G/T	0.000399281	0.0141238	synonymous-codon	HERC1	GRCh38.p7	15:63716426	AATAGTTCGAGTAAA[G/T]GAATGCTCCTGAGGA	8925
rs532865328	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63642774	TAGAAAAAACACTAG[A/G]CTATAAATCAGGAGA	8925
rs532904839	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63676495	AGCGTGGTGGCTCAT[A/G]TCTGTAATCTCAGCA	8925
rs532905180	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63615417	AGTTCAAGACCAGCC[G/T]GGCTAACATGGCAAA	8925
rs532911030	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63776843	CAGTGAAAGTGCACT[C/T]GAGATTTTTACATTT	8925
rs532917498	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63663345	ATAAAACATCAAATT[A/T]TACCTATCACGTGTG	8925
rs532930210	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63816034	GTCCCTCCCCCCACA[C/T]GTAGGGATTATGGGA	8925
rs532940787	in-del	-/TGA			intron-variant	HERC1	GRCh38.p7	15:63697448	AGGTGATGTTAATCT[-/TGA]TTTTTTTTTTTTTTT	8925
rs532944379	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63684414	AAAAATAAACTGTAA[C/G]TGAAATTTTGTCCTG	8925
rs532965464	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63799243	CAGTGGCTCACGTCT[C/G]TAATCACAGCATTTT	8925
rs532979088	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609000	TATAACATCTATGTA[A/G]TTACCATAAAAGTAT	8925
rs532979182	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63755604	GGCAACATGGCAAAA[C/G]CCTGTTTCTTTTAAA	8925
rs532983219	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63733771	GTGGGAGAATCACTT[A/G]AGCCCAAGAGGTTGA	8925
rs532992574	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63636480	TTTACCATGCTGGCC[A/G]GGCTGGTCATGAACT	8925
rs533021547	in-del	-/A	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63762968	TTCCATATAAATGCT[-/A]AAACCATCACAGCTG	8925
rs533039923	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63726228	CTCAGGTGATCCGGC[A/G]GCCTCAGCCTCCCAA	8925
rs533041916	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63823738	TCTTATGAAACCCAG[A/T]TGAAAGAAAAAAAGA	8925
rs533044337	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63712250	TGCACACGTCCACTC[A/G]AAAGAGAAAGTTTAA	8925
rs533045131	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63670322	TTGGAGGGAGAACCC[C/G]TCTTCAGTTGAGAAA	8925
rs533045832	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63830534	TAGAACAAAAAAAAA[A/G]GCATTAATGGGGAAA	8925
rs533081098	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63824265	AGGGCTGGGCGCAGT[G/T]GCTCACGCCTATAAT	8925
rs533083890	snp	C/T	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63669754	ACGAAATAATACATA[C/T]ATCACAATCTTCTTA	8925
rs533129515	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63735233	AAAGGAGTCACATAG[C/G]GAAAGTAAAAGGGTG	8925
rs533138694	snp	C/T	0.00874735	0.0655527	intron-variant	HERC1	GRCh38.p7	15:63706288	ATGTAAGAGATAAAG[C/T]ATCTCTTACATGCTT	8925
rs533144760	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63786136	ATGCACTGCAGTGTG[C/G]CTGTAGTCCCAGCTA	8925
rs533164411	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63766650	AATTTTTTAAGTTTC[A/G]TAATACATTAAAGGT	8925
rs533173068	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63615366	GTAATCCCAACACTT[C/T]GGGAAGCTGAGGCAG	8925
rs533173124	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63622310	AATACCAAGTCTTGA[C/T]GGAAGTGCCTGTTTC	8925
rs533180198	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63712674	TTTTGAAAAAATTTT[C/T]ATATGTCTAAAACAA	8925
rs533205244	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63699071	ACTAGATAAGGCTGA[G/T]TGCTGCTACCATAAC	8925
rs533228154	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63720276	ACTCGGCCTCTTCCC[A/C]TTCTTTAATTCTATG	8925
rs533238752	in-del	-/GCAAAGGTTTGAGAAGG	0.00716266	0.059414	intron-variant	HERC1	GRCh38.p7	15:63637416	ATATGATTTTATCTA[-/GCAAAGGTTTGAGAAGG]GCAAAGGTTTGTACG	8925
rs533278179	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63831251	AGCAGGAATTGCAGG[C/T]ATGCACCACCACGTC	8925
rs533282437	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63799812	TTCTCTAAGCAGGTT[C/T]CAGGAGCCATTCCTA	8925
rs533289740	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63811712	TACTCAGGAGGCTGA[C/G]GCAGGAGAATGGCGT	8925
rs533296587	in-del	-/AGGTGAGGAA			intron-variant	HERC1	GRCh38.p7	15:63736398	CACCAGAAGACTGTC[-/AGGTGAGGAA]ACTCAGGTTTATACC	8925
rs533307188	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63820096	ACTTCATGTAGCACA[A/C]AAGAAATACATACAA	8925
rs533307943	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63793028	AAAGGCTATTACAAA[A/G]GGTATCAATGAACAC	8925
rs533326778	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63679170	ACCAGGCCATCATTC[A/G]AACCAGAACATGACA	8925
rs533329403	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63793398	TTATAATGCATTAGT[A/G]TGCTAAAACACACTC	8925
rs533354129	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63721865	ATTTTCTTTGTTGTT[A/G]TTGCTTGTTTTTTGA	8925
rs533357080	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63823585	TATCTGAACCTCAGA[A/G]CATTGACAATGGTCG	8925
rs533389535	snp	C/G	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63752567	AGAATATTTTCCATA[C/G]CTAAGTGTTCTCTTT	8925
rs533391881	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63721435	GGAGGCTGAGGCAGG[A/G]GAATCGTTTGAACTC	8925
rs533407236	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63644216	TACTATATGTATTCA[C/G]TACCCAAAGATGATG	8925
rs533428553	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63825748	TCATTAGAAAACCAC[A/G]AAAAAAAAGAAAAAT	8925
rs533440229	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63697208	TCCTAGATACCACAT[G/T]GCATTTAGTTGCCAT	8925
rs533456110	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63741876	GCCACTCTATTTTTA[C/T]TACTGTAACTCTAAA	8925
rs533465554	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63819350	TGTCTCACAGAGGTG[C/T]TATTCACATCAATTG	8925
rs533465637	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63826094	AAAAAGAAAACGAAT[A/G]GAATATAAACTCATC	8925
rs533501020	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609347	CCATGACCTCTCCCT[A/G]CCTTCAAGATGGAAT	8925
rs533516276	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63671591	CACTGTATCAGAATC[A/C]CTAGAGAAACTTAAT	8925
rs533533279	snp	A/T	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63680911	TATTTTCAGCATAAA[A/T]AAAAATAACACGAAA	8925
rs533537810	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63787107	TCAGCCTCACAAAGT[C/G]CTGGGATTACAGGCA	8925
rs533540694	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63793136	GGAACTGCCAGAGGC[A/G]TCTGAACCAGAGCAA	8925
rs533557658	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63622959	AGAACAAACCAATTA[C/G]AAGATCATACTGAAA	8925
rs533567364	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63687283	GGTGGCTCACACTTG[C/T]AATCCCAGCAATTTG	8925
rs533574450	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63678568	CCACTGGAATAAGCT[G/T]CCCTGTTATTTACAT	8925
rs533589668	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63773006	ATTGGATTTTATGAG[A/G]CACTCCTGTCCAAAA	8925
rs533614977	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63833969	AGGCGGCGGCAGCAG[A/C]GGCGGCGTCAGGCGA	8925
rs533618207	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63813475	GATAGTGCGAAAGGG[-/T]TTTTTTTTTAATATC	8925
rs533633225	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63621918	CAAGGTTTTTAACTT[C/G]TTTGCCATGGGTTCG	8925
rs533644764	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63737990	GAGCATATTTTCATT[C/T]AATGTATTTTCTATC	8925
rs533644974	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63794633	AGTTATATTCCAGGA[A/G]ACATGAGGAAGACCA	8925
rs533650323	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63827323	GCTACTTGGGTGGCT[A/G]ATGAAGGAGGATCGC	8925
rs533657487	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63729065	GTAGACTCTTTCTAA[A/G]ACCAATCACTGCTAA	8925
rs533670411	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63644855	AAGCTAATTCAGGAT[C/G]ACAATTACTTATATT	8925
rs533671725	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63820674	AAATCAAAAGCAACA[C/G]AGACGTTATCCTTTT	8925
rs533679714	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63744358	CCTGGCTATTGCCTA[C/T]GTTCGCTCAAGACTC	8925
rs533681803	snp	A/C	0.00119808	0.024446	intron-variant	HERC1	GRCh38.p7	15:63788170	GTTAACAAACAAATG[A/C]ATTTGGGTTTCTATT	8925
rs533715983	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63779493	TAGAAACACTAATAA[C/T]GTGAGACATGAATAT	8925
rs533724773	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63825106	TTGAGGCCGGGAGTT[C/T]GAGAGCAGTCTGGCC	8925
rs533734736	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63767303	CCACCGCGCCTGGCC[C/T]ATAGGTTTTAAGTTG	8925
rs533770985	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63760675	CAAAGTATTCAAGAA[A/G]AACTGACAAATATTA	8925
rs533773996	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63773165	TAATCAATGTAGGCC[A/G]GGTGTGGTGGCTCAC	8925
rs533778181	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63781769	AAGCTAAGCCTCTTG[C/T]GCCAGTTAGCCAAGT	8925
rs533782135	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63774214	CTACCTGAAATTATA[C/T]ATTTATTATCTGACT	8925
rs533815117	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63723967	GATGATGAGGTTCTT[A/G]GGCTAGTATCAAAAA	8925
rs533830220	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63821906	TTCTAGTAAGGAAGA[C/T]AAATAATAACCAGGT	8925
rs533842379	in-del	-/T	0.00716266	0.059414	intron-variant	HERC1	GRCh38.p7	15:63695045	TAAAGTATATAATAA[-/T]TTTTTTTTGAGGCAG	8925
rs533847860	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63646385	TATTTTTACATAGAC[C/T]TATCCATGTATATCC	8925
rs533850932	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63731476	ACTTTGTTGTAACAT[C/T]CCTTATAACTTTGGG	8925
rs533851689	in-del	-/CA	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63639680	GTATTTTATCTATGT[-/CA]CAGTTTCTAGAGTAG	8925
rs533862252	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63639303	CTTCTATGTTTACAT[A/G]CACAAATACTTATCA	8925
rs533863551	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63814920	TGTACTAATGTGAGC[C/T]ATGATTATTACAAGT	8925
rs533888304	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63645751	CTTTAAATTCAGTAA[C/T]ACATAACTTATATTT	8925
rs533898407	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63796399	AAACTTAAACTCACA[A/G]AACTGAAACCATCTT	8925
rs533899657	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63745686	TCTTCAGTGCCTCTT[C/T]CAGTGATATGAAGTT	8925
rs533923423	snp	C/G	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63695263	GCGGGTTTTAAACTC[C/G]TGAGCTCAAGCAATC	8925
rs533930720	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63808277	TGGTTTCTTTTTTAG[A/G]ACATCAACGTACTTT	8925
rs533933881	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63745218	GCCTGGCATTGGGGT[C/T]GGGGAGGCGGGGGGT	8925
rs533938528	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63666525	ACTAGATACCGTGAG[C/T]AAAAAGTGTCTTCAT	8925
rs533962919	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63614573	CTAAGAAGGAGCTGG[G/T]AGTGAGGGGTATGGA	8925
rs533977603	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63665794	TAACTAAAATGCCCA[C/T]CTTTTCATATAACTA	8925
rs533977621	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63673571	CATTGACTGAACGAA[C/T]CTCATTTTTATTTCT	8925
rs533980239	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63814679	TTGCCATGTTGGCCA[C/G]GCTGGTCTTGAACTC	8925
rs533984594	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63765291	TACCCCCTTTAAATA[G/T]TGAAGCCCTCAATAT	8925
rs534028055	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63653090	TTTACTTAATAAGTA[C/T]TTTAACATTTTATGT	8925
rs534053855	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63632287	GAATGCCTGGGTTAC[C/G]AACCTACTCAAGATT	8925
rs534071197	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63716131	AGCATCAGAATAGTA[A/C]TAGCACAGTTGTAGG	8925
rs534075210	snp	C/G/T	0.00676609	0.0577691	intron-variant	HERC1	GRCh38.p7	15:63814673	AGGGTTTTGCCATGT[C/G/T]GGCCAGGCTGGTCTT	8925
rs534105114	snp	C/T	1.67716e-05	0.00289578	missense	HERC1	GRCh38.p7	15:63674681	GCTGGACTGCTCTGA[C/T]TTCTGACTGGGCTAC	8925
rs534119126	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63767419	GATAAACAATAAATA[A/G]TACTTTTAAATAAAA	8925
rs534123562	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63734932	GCGAACTCACTGACT[A/G]CTAGGATCATGTAAG	8925
rs534135750	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63776384	ATCCTTCTAGTTCCC[C/T]GAGCCAAAAACTTTG	8925
rs534143431	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63769256	AACCCCGTCTCTACT[A/G]AAAAATACAAAAATC	8925
rs534145868	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63766746	GCAATGGCACGATCT[C/T]GGCTCACTATAACCT	8925
rs534147888	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63653542	TTTTCCTTTTGCGTG[C/T]TGTCCTTCAGTATCT	8925
rs534148680	snp	C/T	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63728385	TATTTCACTATTTCA[C/T]TGTATATCAGGGCAG	8925
rs534162948	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63641981	ACATGACTACAAGGA[C/T]AGCTGCAAAAGAGGT	8925
rs534164130	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63627675	TGAGACTCTGTCTCG[-/A]AAAAAAAAAAAAAAA	8925
rs534217823	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63732191	TTTTTAGTAGAGACG[A/G]GGTTTCACCATATCG	8925
rs534221085	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63648018	AATCTATGCATGTAA[C/T]AAAATTATATTTGTA	8925
rs534221620	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63790031	GAATCTAGGCTATAC[C/T]ATTTACTAGCTGACT	8925
rs534249576	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63702843	GGGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGT	8925
rs534254050	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63739519	GTATTGCTATGGACT[G/T]GCTTACTCTGCACAT	8925
rs534254613	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63782842	TTGATTCTAACCCCT[A/G]CGGATGACTTTGAGA	8925
rs534276320	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63656674	CCAGATCAAGAAACA[A/G]AACATTGCCAGTACC	8925
rs534281454	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63802040	AGTACTTAGAGAATC[A/G]TAAGAGAAAGTGTCA	8925
rs534295196	snp	G/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63809166	ATAGGGATGGAGGGG[G/T]AAGACACAATAGTAT	8925
rs534303151	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63609521	AAGTGAGGAGAAGCT[A/C]TGACTGGCAGGATTG	8925
rs534332138	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63795738	ACACCGAACAAAAGA[A/G]ACAGGGTCATTTATA	8925
rs534336761	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63636522	GTGATCCGCCCACCT[C/T]GGCCTCCCAAAGCGC	8925
rs534358016	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63732597	CTCATTCAGTTCCAA[A/G]TACATTGTTTCATTA	8925
rs534372634	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63755734	TGCAGTGGGCTGAGA[C/T]AGCACCACTGCACTC	8925
rs534378744	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63683051	TGAGGCGGGAGAATC[C/T]CTTGAAACTGGCAGG	8925
rs534385067	snp	C/T	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63703873	AGTGAGCTGTGATCG[C/T]ACCACTGTACTCCAG	8925
rs534403806	snp	C/T	0.00070458	0.0187562	missense	HERC1	GRCh38.p7	15:63656302	AATCGAACTAGCGTT[C/T]GGATATCTGTTAGCC	8925
rs534408583	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63663486	TTAGAGACAGGATCT[C/G]GATCTGTCACTCAAG	8925
rs534445110	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63779127	TTAGAAAAAGATAAG[-/A]AAAAAGAATAATATT	8925
rs534473707	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63736199	CTTTGATTTGTACTG[C/T]AGAATTCCTAGAGGC	8925
rs534480728	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835837	ACCGTGCCCAGCCTG[G/T]TTTTGCCCATTCTAT	8925
rs534485955	snp	A/C/G	1.65891e-05	0.00287998	missense, stop-gained	HERC1	GRCh38.p7	15:63678125	TTTCATTTTCCTCTC[A/C/G]GCTCTGAACCGAGCG	8925
rs534495777	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63685804	TTGCAATGTTGGCCC[G/T]TGGCTGGCATGGGGG	8925
rs534502420	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63754744	GTTACAACTTTAAAA[C/T]AGAATTGAGATTTTT	8925
rs534503048	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63822505	GCAGGATAATCGCTT[A/G]AACTCAGGAGGCAGA	8925
rs534507169	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63829281	AAAAAAATCAGCGGG[A/G]CATGGTGGGTGCACA	8925
rs534515584	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63779767	ACGCCTGTAATCCCA[G/T]CACTTTTGGAGGTCG	8925
rs534534487	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63683666	TTGTTTTTGTTTTTA[A/G]GAGATAGGGTCTCTT	8925
rs534538087	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63737655	AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACTG	8925
rs534538740	snp	A/T	0	0	intron-variant	HERC1	GRCh38.p7	15:63692806	TATAACTATGATGAC[A/T]AAGTATAATAAAGAA	8925
rs534542679	snp	A/T	0.00716266	0.059414	intron-variant	HERC1	GRCh38.p7	15:63790596	AAAAAATTTTTTTTT[A/T]AAAAAGTACTTTTTA	8925
rs534583970	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63695846	ATCCTCCCAAACTCC[-/A]AATCCCTATCCTTAC	8925
rs534599862	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63699192	AAAAATTAGAGCAAT[A/G]TAAGAAAATAAAGGG	8925
rs534605706	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63742599	AATATGATATTAACT[A/G]TAACTTTTTCATAGA	8925
rs534633834	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63786245	GCCACTACACGCCAG[A/G]CTAGACAACACAGCA	8925
rs534639770	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63706440	AAAACATGGAAAATT[A/T]TGTAAATAACCCCTT	8925
rs534642425	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63724004	CAACCCATAGTATAA[C/G]TGAATTATTGTATTT	8925
rs534644457	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63793541	AAAACTCATGAATAA[C/T]TCACCCCTTGTTTAG	8925
rs534666959	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63672071	TTGCTCGAAATTTTT[G/T]TAAGAATAAAAATAC	8925
rs534673440	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63711141	GAGTTTAAGATCAGC[A/C]TGGGCAACAGAGCAA	8925
rs534687208	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63804810	TCACCAAAGATACAT[A/G]AACAGCCAAAAAAGC	8925
rs534690987	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63773164	CTAATCAATGTAGGC[C/T]GGGTGTGGTGGCTCA	8925
rs534726882	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63712451	CACCTACTAAAATAG[A/G]GAATAAAAGAGAAAC	8925
rs534739079	snp	A/G	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63806294	CAATCTTCCCACCTC[A/G]CCTACATAATCTTTA	8925
rs534755587	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63759178	AAAGACAAGAATCCT[A/G]TGATTCTTGAAACAT	8925
rs534755982	in-del	-/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63754448	TAACTGAAAAATAAA[-/C]TTTTTAAAAAACTCA	8925
rs534764339	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63659529	AAGTGCTGGGATTAC[A/G]AGCATAAGCCACCAA	8925
rs534764858	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63687157	ATCTCTGATCACATC[C/T]GTGCTTTATAAACAT	8925
rs534776101	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63718170	TGAATATTTTTGATA[A/C]TTTCTAGTCCTTCTA	8925
rs534810102	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63721442	GAGGCAGGAGAATCG[C/T]TTGAACTCGGAAGGC	8925
rs534812858	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63820388	TTATATAACAAAGTT[C/T]AATGATACTTCATAA	8925
rs534832952	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63678762	GTTCAAGGGGTGCAA[A/G]AGTAAAATCATAAAG	8925
rs534846493	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63801205	CCAGTCATTGTAAAT[A/G]GGATATTTCCCGTGT	8925
rs534855438	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63637949	AAGAAGCAGAAACTC[A/G]TACATAAGAATGAGT	8925
rs534860750	snp	C/G	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63825851	CACTGCAACCTCCAC[C/G]TCCTGGGTTCAAGTG	8925
rs534893348	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63644423	AAAAAATAAAACAAT[C/G]TGGTAACAACAGGCT	8925
rs534898248	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63656577	GGCATATACTTGAAG[C/T]ACAATTGAACTGACA	8925
rs534913712	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63793166	ACTCCATCTTGAGTA[C/G]GGACTGTGTAAAATA	8925
rs534914540	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63689232	ATTTAGCAACAAACA[C/G]TTATCTTTGTCATTT	8925
rs534925896	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63825375	TTTTCTAAAAGTAGA[C/T]TTTAAATGTTCCTAG	8925
rs534947183	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63610800	CCTTACTGTTTTCTG[A/G]ACAAACATCATGGGC	8925
rs534969761	snp	C/T			stop-gained, intron-variant	HERC1	GRCh38.p7	15:63662994	CACACCCAGGTAGGC[C/T]AATCCAGTACCTCTG	8925
rs534979741	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63707803	GTGTGGTAGCACACG[C/T]CTGTAATCCCAGCTA	8925
rs535005979	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63800773	AGGGGAATAGGAGCA[C/T]CTTTTGTTATTCGTA	8925
rs535010616	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63743023	TATTAGCTTCTCTTC[C/T]ACATTCTGGAAGAGT	8925
rs535017320	snp	C/G	0	0	intron-variant	HERC1	GRCh38.p7	15:63715033	ATAAACCCTCTCAGA[C/G]TCCAGAGCTAGAAAT	8925
rs535034972	snp	A/G	0.00636936	0.0560724	intron-variant	HERC1	GRCh38.p7	15:63627599	GAATCGCTTGAACCC[A/G]GGAGGCAGAGGTTGC	8925
rs535038005	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63758039	TTAAAATGAAAAAAA[A/C]TAATGCAGTATATAG	8925
rs535066270	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63722364	CACATCCTTTCAGTC[A/G]TTAAACCATGGCTTG	8925
rs535072852	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63667159	CAGTATGTATTAAAT[A/G]TGGTATCTTTAAACA	8925
rs535089441	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63767996	GTTGTCATAGTCTCC[A/G]TTATCGCCCCACCCC	8925
rs535119890	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63809467	AGATACATAAGCAAT[C/T]ACAGTACAATATGAT	8925
rs535145904	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63630035	ACTTTGTATGCCATC[A/G]TATTATAAAATATAA	8925
rs535149249	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63714783	CGAACTCCTGACCTC[A/G]TGATCCGCCTGCCTC	8925
rs535154308	snp	A/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63717584	TTCGGCCAGGTGAGG[A/T]GGCTCACGCCTATAA	8925
rs535171027	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63822446	CAAAAATTAGCCGGG[C/T]GTGGTGGCGTGTGCC	8925
rs535177763	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63794136	ATGAATAATCCACCC[C/T]TTGTTTAGCATATCA	8925
rs535182712	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63724948	AGTCATGGTTAAGTA[C/T]TCTTACAGTGCTTTA	8925
rs535185264	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63743862	ATGGATGGTGTGGAT[A/G]CCAGTAGATATTGAA	8925
rs535215863	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63682439	TAGCTTGTAGTTGCT[A/C]TCTCCTCCAGTGGGA	8925
rs535215897	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63765214	TATTCTGCTCCTTTT[C/T]TCTTGCAATTTGTGG	8925
rs535221815	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63730333	GCATGGTGGTGCACA[A/C]CTCTAGTCCCAGCTA	8925
rs535227280	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63750724	ATCACCCAAGCTCAG[C/G]AGTTCAATACCAGCC	8925
rs535227912	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63648506	AAGTCACCATAGGTT[A/C]TTTCCTTTTGGACCA	8925
rs535240171	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63701867	GTTTGCTCTGTACTA[G/T]CTGAATACAGGAAAT	8925
rs535242418	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63775723	AAAATTTCATCTTAC[A/G]TTACAATTAATGATT	8925
rs535254182	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63797014	AGTTTATCAGGTTAA[C/G]TTTGGAATGCTTGCT	8925
rs535265035	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63751418	CTCACAATAACAAAA[A/T]GGCCTAATAACACAT	8925
rs535288638	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63697433	GACATGACTTAATAC[A/G]GGTGATGTTAATCTT	8925
rs535301299	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63704027	TTTGAATGGCTCCCA[A/G]ACAGTTCTCAGACTT	8925
rs535337280	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63707452	GGAAGTATATTTCTG[G/T]GTGTTACCTGTGTAT	8925
rs535343781	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63809945	GCCTCCCAAAGTGCT[A/G]TGATTACAGGTGTGA	8925
rs535353408	snp	A/T	1.65965e-05	0.00288062	synonymous-codon	HERC1	GRCh38.p7	15:63623827	AGGCAGGCGGAGGTC[A/T]GAAGCATTCAGCTTA	8925
rs535353658	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63657457	TTTTGTGAAACACTT[A/C]TTAATGTGTTTTGTC	8925
rs535398784	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63619723	CTGGTTTAGTCTTGG[A/G]AGAGTGTATGTGTCG	8925
rs535409700	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63817399	GAAAGGTAAACATTA[C/T]GTATGTCAAGGATTT	8925
rs535411900	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63660409	CCACATAATGAACTA[C/T]GGCACCATCTCCTGA	8925
rs535416720	snp	G/T	0	0	intron-variant	HERC1	GRCh38.p7	15:63733426	AGTACTGTAAGTAGA[G/T]AGGAGTACGAAATGC	8925
rs535453454	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63768574	ATCTGTGGCTTCGTT[A/G]TCTAAAAGCCAACTC	8925
rs535470724	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63626939	AGGTGCTATTATTAT[C/T]CTCATTTTACAGACA	8925
rs535476112	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63816325	CCCTTTTGTCAAGGA[C/G]CCACATTGGGAAATG	8925
rs535483847	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63830832	CAGTCCCATTAATTT[A/G]GAGAGCCCGGTAGGC	8925
rs535487822	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63776958	TAGTTTATTTTGAAA[C/T]GCATCAGAAATAAGA	8925
rs535510295	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63823867	TAACAAAATGAAAAC[A/G]TAGCCTACGGATTTG	8925
rs535510364	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63829439	AAAAAGAAAGAAACG[C/T]CAGTATGTGTGTGTG	8925
rs535515625	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63704770	TTGAGATGGAGTCTC[A/G]CTCTGTCGCCCAGGC	8925
rs535518939	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	HERC1, FBXL22	GRCh38.p7	15:63608322	GTCCAGAGAAGGATG[C/T]GTGGTACTGAGAGGG	8925
rs535542155	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63822799	AGAATAAGGCAGAGA[C/T]GACAAAATGTGATCA	8925
rs535546032	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63632505	TGGCTCTGGCATAAG[C/G]GGTCTTAATGGGGAG	8925
rs535557419	snp	A/C	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63724293	TATCATGTTAAAGAC[A/C]CCTTGAAAAACCATG	8925
rs535559682	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63641359	TTCTGCCCAAATAGC[C/G]CCACTTATTATCCTC	8925
rs535577169	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63642181	TTAAGGGTATGAAAA[A/G]TAATACTGTAGGGAA	8925
rs535589663	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63734011	CTATAAAAATAAGAA[A/G]AAAAAATTAGCCGGG	8925
rs535596667	snp	A/G	6.68382e-05	0.00578054	intron-variant, synonymous-codon	HERC1	GRCh38.p7	15:63654361	AAGGATGGGCATACA[A/G]TTGGGCAATTAAACC	8925
rs535607214	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63740240	TAGAAGGTTCGGTTA[C/G]GTTGTAGTATGTATC	8925
rs535609154	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63678731	CCAGAATGATGAGTC[A/C]TGGACATTTTACATT	8925
rs535622520	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63821091	AAGAATTCACAGCAT[C/T]GTTTAACTGACTCAA	8925
rs535656384	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63675990	CTCACTGCAACCTCT[G/T]ACTACTGAGTTCAAG	8925
rs535677790	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63613851	AATAAAAAACTGGCA[C/T]TAAGGTTGTCCCATA	8925
rs535678200	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63754894	CCCCTCACAGCACTT[A/G]CCTTGTGTTGTCCTG	8925
rs535678590	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63628988	TGGAGTCTTGCTCTG[C/T]TGTCCAGGCTGGAGT	8925
rs535680605	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63621593	CTGCAGAGTGTTTTC[C/T]AACTTGGTTCCATTC	8925
rs535690614	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63611922	AGGCGTGTTGGCTCA[C/T]GCCTGTAATCCCAGC	8925
rs535692830	snp	C/T	0.0592355	0.161582	intron-variant	HERC1	GRCh38.p7	15:63620647	TCTCTTTGTAGGTCA[C/T]TAAGGACTTGGTTTA	8925
rs535730757	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63660907	GGTGAATTTTAGTAA[A/C]AGATGTTAAGCAGAG	8925
rs535731665	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63727232	AATGAGGCAAGATTG[C/T]GCCACTGCATTCCAG	8925
rs535735358	snp	G/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63628523	TGCTATGAAAATACT[G/T]CCAGTGCTAGTAGCA	8925
rs535740202	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63817243	ATCTATATCTATCTA[C/T]AAACCAGAGAAATAT	8925
rs535769330	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63668053	CAAGGGTCAACTGTA[C/T]AGCTAATAAGCCAAC	8925
rs535804309	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63642932	CAAGCTTACACCCTA[A/T]CATTTGATATAACTA	8925
rs535814038	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63684536	CTAGATAAAAATAAC[A/G]AATGATTTTTAAAAA	8925
rs535816292	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63769651	CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC	8925
rs535823643	snp	G/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63784609	TTATCATGCAAATTT[G/T]TTTTTTTTTCCTTTT	8925
rs535826964	snp	A/C	0.0103295	0.0711199	intron-variant	HERC1	GRCh38.p7	15:63662278	TGAGAAGAGTTAATG[A/C]ACATGACAATCTGTC	8925
rs535827588	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63823172	TTTCCACTCTCCAAT[A/G]GGCCCCAGTGACTGT	8925
rs535832993	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63833301	CACCCAAAGGCAGAG[C/G]AGAGGAGGAAGACAC	8925
rs535849856	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63715604	TTAATTGACAGATAC[A/G]GACAATCTCAAAACC	8925
rs535849868	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63698026	TTTGCTCACTCATTT[G/T]AGCATTCAACAGTGG	8925
rs535862972	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63785223	TAGGCCAGGAGTTCA[A/G]GACCAGCCTGAGCAA	8925
rs535887888	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63693469	GGCTGATCTTGAACT[C/T]CTGGGCTCAAGCAAT	8925
rs535902523	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63697920	GGGAGAACTATGGAA[A/G]AATTGTGGACATGTT	8925
rs535916371	in-del	-/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63770268	TTTCAAATAACCTCA[-/G]GGGGTACTTCCTCCG	8925
rs535932375	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63750495	ATCAGCAATCTGAAT[A/G]ATTTTTTTTCTTTAT	8925
rs535937178	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63642397	GGTTGGAGTACAATG[A/G]CGCAGTCTCGGCTCA	8925
rs535952035	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63790798	TTTTTTTTTTAATTC[G/T]CTGTACTTCTCTTCA	8925
rs535964037	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63800758	AATTTCCTTTGTGAT[A/G]GGGGAATAGGAGCAT	8925
rs536000982	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63639070	TGGAGGACCCCACAC[C/T]CCTGTAAACTCTTTG	8925
rs536002679	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63613940	CAAAGTCTGCCAAAC[A/G]AAAACAAAAACGAAC	8925
rs536015878	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63669945	GCAGGTTGGGGGAAT[A/G]CAGCCATTAGCAAAA	8925
rs536029105	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63770282	CAGGGGTACTTCCTC[C/T]GTAAGACATTTTCGG	8925
rs536042120	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63672810	AAATATATTTCACAA[A/G]CATCAATTTCTATGA	8925
rs536043200	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63813764	TGCCTATCAATGTCC[C/T]CTTTCAAGAATACAG	8925
rs536057389	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63802292	AAAAAGAAAAAACTT[C/T]TTCGTTGTTATTATT	8925
rs536058932	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63766738	GCTGGAGTGCAATGG[C/T]ACGATCTCGGCTCAC	8925
rs536064725	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63763983	GAGGTAACAACTGGT[A/G]CCACTTCCTTTTGTA	8925
rs536068959	snp	A/G	1.68199e-05	0.00289994	synonymous-codon	HERC1	GRCh38.p7	15:63624310	CCAAGTTCCAGCATT[A/G]TAATGGGATGTGCTG	8925
rs536070966	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63631738	TAGAGACGGCGTTTC[A/G]CCATGTTGGCCAGGC	8925
rs536098821	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63811412	ATCTAGGTGAAAAGC[A/G]CTATTCTTCATTTTT	8925
rs536106509	snp	A/G	0.000535666	0.0163568	intron-variant	HERC1	GRCh38.p7	15:63723152	TATGAGCTAACTACA[A/G]ATTTACTCCCTTTAT	8925
rs536113390	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63824385	AAAAATACAAAAAAA[C/T]TAGCCGGGTGTGGTG	8925
rs536131732	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63631164	TAAGTTTCTTATATT[A/C]TAAAATGAGAGATCA	8925
rs536149058	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63817970	ATAGATTAATCCAGA[A/G]TCAGGCACAAGTGAG	8925
rs536157545	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63821116	ACTCAACAGTCCTCC[C/T]TTAGCTTAAGAATTA	8925
rs536157824	in-del	-/A	0.41833	0.184838	intron-variant	HERC1	GRCh38.p7	15:63625693	GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA	8925
rs536159409	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63639165	GTTGGGCCAAATGGG[C/T]TTAGAAGGACATTTT	8925
rs536160715	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63729987	GCCAAGATCACGCCA[C/T]TGCACTCCAGCCTGG	8925
rs536162093	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63810728	ACGTGATCTCAAAAT[A/G]CCACCACCTAATTGT	8925
rs536190480	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63776277	TCTCAAAATTAACAT[A/T]TCCAAAACTGAGCTC	8925
rs536194559	snp	C/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63780870	TAACTGAATAAAACA[C/T]ATATGAAAGTAGTTA	8925
rs536197405	snp	A/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63676213	AGCCTACTGTATGCA[A/T]CTTAACCAGGCATCA	8925
rs536231767	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63808955	GAACTCCCAATGTTA[A/T]ATCCAATTGATACTT	8925
rs536239334	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63760415	CACTGTACTCCAGCC[A/C]GGGCAGCAGAGACAC	8925
rs536272390	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63653244	TCAGGAGTTTGAGAC[C/T]AGCCTGGCCAACATG	8925
rs536272425	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63685894	GGCTTATTGTATCTA[C/G]ATTGTACAAACAATA	8925
rs536292522	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63612010	GCCAACATGGTGAAT[C/T]CCCGTCTCTACCAAA	8925
rs536302168	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63692945	CAGCACTTTGGGAGG[C/T]CGAGGCGGGCGGATC	8925
rs536304549	snp	C/T	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63617835	TCTGTTCATATCTTT[C/T]GCCCACTTTTTGATG	8925
rs536318215	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63738153	ACATTATTTCTGTGG[C/T]ATTCTTGCCCAAAAT	8925
rs536345824	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63628531	AAATACTTCCAGTGC[A/T]AGTAGCACAAAGAAT	8925
rs536352061	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63651746	GCTGGCTATAAAACT[A/T]TTAAAAATGCGGCTG	8925
rs536363104	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63625040	TTTCTTCCACTAATT[A/T]CAGTTTGCTAACACT	8925
rs536380111	snp	G/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63742777	TATATTGATTGATTT[G/T]CATACTTTGAAAATG	8925
rs536387169	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63650670	ATGTACAAATGTCAA[C/G]CACTTAAGTCCTTTC	8925
rs536421531	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63782102	CAGCAAGTGCTGATG[A/T]AGAAGCTGCACAAAG	8925
rs536429717	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63681800	AAACATCACACACAT[A/G]TTATTTTTCTTGCTG	8925
rs536431387	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63665181	AGGGGCATCTTCTAC[C/T]AGATATTAAAAACTA	8925
rs536470358	snp	A/G	0.000399281	0.0141238	synonymous-codon	HERC1	GRCh38.p7	15:63680768	TCTGTTTTCCTTCAC[A/G]ATATAAAACTAAAAT	8925
rs536503434	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63695679	AGGTGTGAGCCACCA[C/T]GCCCGGCCGAGTCTG	8925
rs536528591	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63722636	ATGATCTACTGCTGC[A/G]GTATCACAGTGATTG	8925
rs536551737	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63813833	AGCACTTTGGGAGGC[C/T]GAGGCAGGTGGATCA	8925
rs536576456	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63745121	GTGACCAAGATGTTA[C/T]CTAAGACACAAGACA	8925
rs536593982	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63711270	TTCGAGGCTGCACTG[A/G]GCAGCCTGAACTCCA	8925
rs536596213	snp	G/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63773335	TGTAATCCCAGCTAC[G/T]CGGGAGGCTGAGGCA	8925
rs536608249	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63794934	AGCCAGGCGTGGTGG[C/T]GTGTACCTGTAGTCC	8925
rs536614835	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63747156	GTTTGGGTAACATTT[C/T]TATATCTTTAAAAAT	8925
rs536619018	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63744613	GCTAGAGGAGCCTCG[C/T]CCCATAGCTACCACC	8925
rs536619784	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63662423	TTCACTTATTTATAT[A/T]GCAGATTCTCTTTCC	8925
rs536624050	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63655417	TGATGAAGAGAAAGG[C/T]AGTACTGATAAGTAG	8925
rs536629729	snp	C/T	1.65594e-05	0.0028774	synonymous-codon	HERC1	GRCh38.p7	15:63612482	ACACACCATCTGCTC[C/T]AGTTGTTTTGCTGTG	8925
rs536636877	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63698088	TCTAACCTGAAGCAG[A/G]TGTCTAATTTAAACT	8925
rs536642791	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63782748	TGGAAAGGATTCACC[A/G]TTGTAGATGCCATTA	8925
rs536657278	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63666175	GGAAAAACAGTCTGA[C/T]GCTGACTTTGGGCAA	8925
rs536660767	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63661580	TTGCTATGCCATTAT[A/T]CCTGGGAACATGAAT	8925
rs536676213	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63709330	TTTTTTAAAAATGGG[G/T]TTTTTTTTAGTCTTT	8925
rs536680734	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63705026	TACAGGCATGAGCCA[C/T]GACACCCCACCCTCT	8925
rs536693573	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63618628	TATTGATTCTTCCTA[C/T]CCATGAGCATGGAAT	8925
rs536702352	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63763237	AGAAACGATAGAATT[A/G]GAATATCATATTTTT	8925
rs536721192	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63724330	CTTTCTTTAACAAAA[C/T]GTTTCATAAACACCA	8925
rs536762623	snp	A/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63620861	GTAGATCTTCCTCCA[A/T]CCCTTTATTTTGAGC	8925
rs536774670	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63801432	CAGGGACAGCCCGTT[A/G]GTATCTGGAAAGTTG	8925
rs536802684	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63739388	TTTTTAGTAAAAAAG[A/G]GTTTTACCATGTTGG	8925
rs536813369	snp	A/C	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63647510	CTGAGTATCTACCCA[A/C]AGGAAAATAATTCAT	8925
rs536817251	in-del	-/A	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63672183	ATTTACTTTTTGAGG[-/A]AAAAAAAATACTCAA	8925
rs536830284	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835253	TGTAAAGCTCACATA[C/T]GGCACATATTAAGTA	8925
rs536834011	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63688669	ATGAGAACAGGCCAT[C/T]CTATCAAAGTAGGAG	8925
rs536837413	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63623162	TGAAAAGAGTGTAGT[A/G]ATGTTCAAATCGAAT	8925
rs536843616	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63684736	TGTTGGGCCAGGCGC[A/G]GTGGCTCACACCTGT	8925
rs536845310	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63828138	AATTGTATGGCAATA[A/C]GTAACTGTATCAGAA	8925
rs536855264	snp	G/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63778308	GACTCCCAGAAAGAT[G/T]AAATCCACACCGTAT	8925
rs536858422	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63726960	TGATAGACTGAATCT[C/T]AGCAAGTTCTGAGAC	8925
rs536877149	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63691369	TACTTGGGAGGCTGA[A/G]ACGGGAGGATCACTT	8925
rs536877868	snp	A/C	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63828614	AAAGTGCTGGGATTA[A/C]AGGCATGAGCCACCG	8925
rs536880689	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63822023	TTTACACTGTATTCA[G/T]TGAAGATCTCTCTAC	8925
rs536981742	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63649121	GGACTTTGGGAGGCC[A/G]AGGTGGGCGGATCAC	8925
rs536990706	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63796247	GGGTATCATCCCTTA[A/G]GTCCATATGCCAACA	8925
rs537022424	snp	C/T	0.000798403	0.0199641	downstream-variant-500B, utr-variant-3-prime	HERC1, FBXL22	GRCh38.p7	15:63608545	TGGAAGCTCATTCTG[C/T]TCTGGGCTAATGTCT	8925
rs537063409	in-del	-/A	0.184203	0.241186	intron-variant	HERC1	GRCh38.p7	15:63760436	GCAGAGACACCATCC[-/A]AAAAAAAAAAAAAAA	8925
rs537068491	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63772300	GAAGGTAAGGTCCTC[A/G]AGGAAGAGGCTTCTG	8925
rs537085830	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63712318	CATTGGAGACACACT[A/G]ACGGTAAAATTTTTA	8925
rs537087536	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63812276	ACAACCTTCCATCTC[C/T]TAAATCTTCAACCCA	8925
rs537104668	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63621475	CAATTATGTGTCTTG[A/G]AGTTGCTCTTCTCGA	8925
rs537109307	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63677014	TGGATTTCAGATTTT[A/T]TTCCCAAATTTTGGA	8925
rs537114089	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63711579	ATGGAAGCTTTTTTA[A/C]AACAATAACTTATTC	8925
rs537120043	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63810683	GGATGCTAAAACCAA[C/T]GGGAAAGCGTTGTAG	8925
rs537152858	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63719121	TATTATTGTTAGGAG[A/G]AGCAGGGTGGGAGAT	8925
rs537167262	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63811354	GTATGCATGTTTAGA[A/G]GGGAGGAAAAAAGCA	8925
rs537174271	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63727443	TTTCCAACTCCAATG[C/T]TTTTCCTTTTATGCT	8925
rs537177747	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63706902	TTAAGATTTAATAGA[A/G]TATTAGAATAGAAAT	8925
rs537193538	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	HERC1	GRCh38.p7	15:63668939	CTGCTAAACAATTTA[C/T]AGAACACTCAACAAC	8925
rs537197347	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63787777	CTTACTAACCTGGAC[A/G]ATATGGCAAAACCCC	8925
rs537204058	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63741958	TTTCAAGACTGTTTT[A/G]GCTACTCTGGATCCT	8925
rs537205319	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63734495	TAGTACCATAAGAAA[A/C]ACTGGAAAAATTAGT	8925
rs537280733	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63831498	TCCAACTATAACATT[C/G]AAGTTTTGTTTCACA	8925
rs537282024	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63707332	TCTGGTAGTATTTGA[A/G]AAGATTTTTAAATGT	8925
rs537300139	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63623006	AATTTATAATGCCAT[G/T]TGACAACCAACAATT	8925
rs537316174	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63747487	ATTTTGTCAAGTCAT[A/G]AACAACAGTAATTTT	8925
rs537316921	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63706601	AAAGAAAATAGTCTT[C/T]GTTTTAACTCTTCTG	8925
rs537319389	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63713827	AACTTAGTTAAAATT[A/G]CATTTAAAATATACT	8925
rs537320571	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63698515	TTCTGAGTATATTGT[C/T]CTGAGAGATGACAAT	8925
rs537321160	snp	A/G	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63805624	GTGAATTTATGGTAT[A/G]TTAATTATACCTCAT	8925
rs537340652	snp	C/T	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63741403	GATCTCAGCTCACTG[C/T]AACCTCCGCTTCCTG	8925
rs537342001	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63638630	AGCCTGTATGGGAGA[C/T]ACCAGGGCACAAACA	8925
rs537348573	snp	C/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63705781	CATACAATAATCCCA[C/G]CACTTTGGGAGGCCA	8925
rs537348917	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63649308	CAGTGAGCCGAGATC[A/G]CGCCACTGCACTTCA	8925
rs537353999	snp	C/G	0.00597247	0.0543191	intron-variant	HERC1	GRCh38.p7	15:63721497	CGCCACTGCACTCCA[C/G]CCTGGACGATAAGAG	8925
rs537369734	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63631041	TACAGTGCAGTGGTG[C/T]GACCTCGGCTCACTG	8925
rs537388577	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63671431	ATTCCTCTATCTTCC[C/T]TATTCTTTGAACAGA	8925
rs537448957	in-del	-/GA	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63675996	CAACCTCTGACTACT[-/GA]GAGTTCAAGAGATTC	8925
rs537467117	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63681581	GGTAAAGTTTCTTAC[A/G]CTGATTTAAAAAAAA	8925
rs537497525	snp	A/G	6.72235e-05	0.00579717	intron-variant	HERC1	GRCh38.p7	15:63651242	TTTACTAGTGTTTAC[A/G]TGACTCTTACCATTA	8925
rs537502241	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63720677	GCCCACAGAGAATCT[C/T]AGAATGACAATCCTC	8925
rs537507248	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63687866	CATATCTAGAGGTAA[C/T]AGCCAGTTTAAAGCC	8925
rs537516206	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63828026	GGGGTGATGAAAGTG[C/T]TCCGGAATTAGATAG	8925
rs537532753	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63731574	TCCTTAACATCAGAT[A/T]AAATTTACATTTTTA	8925
rs537534265	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63637877	ATAGTTTAGAACAAC[A/C]AAATGGATGAAAGAA	8925
rs537534270	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63629207	CACCCACCTTGGCCT[C/T]CCAAAGTGCTGGGAT	8925
rs537581216	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63676474	TTTTAGATATTGTTC[C/T]GGCCGAGCGTGGTGG	8925
rs537587124	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63781876	TCGCCTTTTTCCTGA[C/T]ATGGGGAAAGTCTGA	8925
rs537595377	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63802989	CCAAGGTGGGAGGCT[C/T]ACTTGAGCCCAGGAG	8925
rs537600555	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63621605	TTCCAACTTGGTTCC[A/G]TTCTCCCACTTTCAG	8925
rs537625020	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63831910	TGGAAATGGAATACA[G/T]GACCAGCAAATGAAT	8925
rs537645187	snp	G/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63700036	AGTAACTTCTATCTA[G/T]TTGCTCCTCCTCCAG	8925
rs537651745	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63656890	AGCATTGAGCAGTTC[A/G]TTTTCATTGACATAT	8925
rs537671329	snp	C/T	1.66313e-05	0.00288364	synonymous-codon	HERC1	GRCh38.p7	15:63753033	CATTCCTTGTAAAGC[C/T]TCAATAACTTTAGGT	8925
rs537679991	snp	A/C	6.76796e-05	0.00581681	intron-variant	HERC1	GRCh38.p7	15:63749802	TAGACCTGAAAAAAA[A/C]AGAAATACGTTACAC	8925
rs537701332	snp	C/G/T			intron-variant	HERC1	GRCh38.p7	15:63808419	CAGCATCCTGAGTAG[C/G/T]TAGGACTACAAGCAC	8925
rs537702264	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63767893	CTCTCCTCACCCCAG[C/T]AAAGCTGCAGAGAAG	8925
rs537704865	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63616080	GCTACTTGATCAGCA[A/G]GAATGTGATGACTCA	8925
rs537726890	snp	A/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63717545	GCTGCAAGAATTACT[A/T]CTGGACTGTTCTTAA	8925
rs537726949	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63709594	CAGGTCAAAGTCCAT[A/G]GTGAGTTTTAACCCT	8925
rs537735143	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63815675	GTGAAGTCAAACACA[C/T]TCTTCATGGTTGGAT	8925
rs537742521	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63695969	CACCTAATCTCTACT[A/G]CATTATTTAGGAAAT	8925
rs537762426	snp	C/G			upstream-variant-2KB	HERC1	GRCh38.p7	15:63834575	TGCCAGGGCCTGGCT[C/G]CTCGGTTTTCTTTTC	8925
rs537763819	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63716747	TATATTGCTATTCAG[C/T]TATAAATTCCTACAG	8925
rs537767980	snp	A/G	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63622593	CCGCCTCAGCCTCCC[A/G]AAGTGCTGGAATTAC	8925
rs537775107	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63809241	AAAATAAACAAAAAT[A/G]AAGGCATGAACCCCT	8925
rs537806514	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63641712	GCTATCACCATTTAA[A/T]CTGCGAAATTCCTTC	8925
rs537841296	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63705325	CGCCTAGCTTTTTTT[C/T]TTCTTTTTGGCAGAG	8925
rs537853007	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63783595	TGCTTTACTGTACTT[A/T]TCGCTTTATTGCAGT	8925
rs537904999	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63681116	TAGATTTTAACTACT[C/G]TCTTGCATATACCTC	8925
rs537920495	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63696498	TATTACTTTTTTTGA[A/T]GATTTTCTAAAAACT	8925
rs537920977	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63640623	CCGAGGATTTCTGTA[C/T]ACCCTTCGCCCAACT	8925
rs537923571	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63680251	AATTGAAAGCTTTTA[C/T]GAGACAGAACAAAAG	8925
rs537957919	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63639803	ATAAATTAGAATCTA[C/T]ATGTGGCATATAACC	8925
rs537988324	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63707991	ATTTGGAAAATGTTA[C/T]ATAAAATCTTTACCT	8925
rs538008402	snp	A/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63660327	TCCATCTCAAAGAAA[A/T]AAAAACAATAAATAA	8925
rs538024373	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63687853	AATTTCTAAGAAACA[C/T]ATCTAGAGGTAATAG	8925
rs538035673	snp	A/G	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63764416	AAGTGCCAATCCCTC[A/G]CTGATTACCTGATTA	8925
rs538038343	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63668451	TGACCCAAGGTCACT[C/G]CAGCCCGGGTGACAG	8925
rs538047161	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63770809	GAGAAATTCAAGACG[A/G]GGAGGATCAGGTCAG	8925
rs538053075	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63788831	TGGGGCAGGAGATCG[C/T]GCCATTGCACTCCAG	8925
rs538054277	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63760899	AAAATTACTGATCTT[G/T]AAAGAGAAAAAAAAA	8925
rs538055979	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63728278	TAGTGAGGGAATGCT[A/T]TCATATTTTTTAAAC	8925
rs538066339	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63769567	GAAATTAAAATAAAT[G/T]TTGGGGCCCGGTGTG	8925
rs538074871	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63675283	GAAAAACGAGTCTAT[C/T]ATGAGAAAATGGGGA	8925
rs538080246	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63635860	TTATAATTACTGTGT[A/G]ATATATTTTTACTAT	8925
rs538088145	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63767830	CAAGTTCTCCCTCTG[C/T]CTTCAAAAGCTGCTA	8925
rs538089884	snp	A/C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63812766	ATCTACATGCTAAAA[A/C/G]TTATAAAGAAAAAAT	8925
rs538095848	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63761173	AGTCTTTATTGAGAA[A/C]TCTACTAGAGAATGA	8925
rs538101647	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63626859	CTGAGTACCTTCTAT[A/G]TGCCTGGCACTATTC	8925
rs538134201	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63733290	TAATTATAAAAACTA[C/T]CCAATTAATCCCATT	8925
rs538142112	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63634707	AACAATGATCAGCTA[A/G]AATATCTTATTGATT	8925
rs538157017	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63724831	AAAGGCACTTTAAGT[A/G]GCGAAGAAAAAATTA	8925
rs538174470	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63736213	GTAGAATTCCTAGAG[A/G]CTCATATACTTCTGC	8925
rs538179010	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63732846	TTTCTATCATAGGTG[A/T]TTAAATGTCAAAATA	8925
rs538188962	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63649036	CCTTCCTCCATTACT[C/T]CAATTTTACTCATTT	8925
rs538193188	snp	A/C/G			intron-variant	HERC1	GRCh38.p7	15:63612059	CAGGCGTGGTGGCAC[A/C/G]CACCTGTAGTCCCAG	8925
rs538196406	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63648299	ATGATAATGCAACCA[G/T]TGCAAGTAAATTTCC	8925
rs538198992	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63776480	AACATATATCTAACC[C/T]TATGACCCAACAATT	8925
rs538213043	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63650600	CTGTAACTATTAATA[C/G]GGCAAAATGGTAGCG	8925
rs538238495	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63689358	TACTACAGGACAAGA[C/G]AGAAGACAGAGAAGA	8925
rs538246830	snp	A/T	0.000134131	0.00818827	synonymous-codon	HERC1	GRCh38.p7	15:63749375	CTCTTACCTGTCCCT[A/T]GGAAGAGCAGTCCAT	8925
rs538247184	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63742232	TTCCTAAGTATCCTA[C/T]TCTTTTTGATGCTTT	8925
rs538254991	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63609970	TTTGTACAATTGAGG[C/T]AAAGACTATGAGGAA	8925
rs538266580	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63697318	TATATTTTGTAGATG[C/T]CCCTAAATTTTGGGT	8925
rs538275121	snp	A/C	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63688873	CAATCAGAAATGGGA[A/C]AAAAAAAGGGGCTGG	8925
rs538284109	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63699963	TCCATGCATGGCCCA[A/G]TTTTGAAATCACATA	8925
rs538297900	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63776789	TGGACAACACAGTGA[A/G]ATCTCGTCTCTACAT	8925
rs538303197	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63703871	GCAGTGAGCTGTGAT[C/T]GCACCACTGTACTCC	8925
rs538317238	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63757796	CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG	8925
rs538318935	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63707188	GAAGTAGTGCCTTAT[G/T]TTCCAAAATTACTAC	8925
rs538325863	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63803504	CATAATTCACTGAAG[C/T]CTTGAACTGCTGGGC	8925
rs538333871	snp	C/T	0.000365661	0.0135165	synonymous-codon	HERC1	GRCh38.p7	15:63654254	TTGCTGAGCTGCCCA[C/T]TGCCGATGCTGTGAG	8925
rs538336300	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63614354	TAACTATGGGAAAAA[C/T]GGCACCCAAGAGTGC	8925
rs538351619	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63806063	CAGTATATATTTTTT[C/T]TTAACATCAACCACT	8925
rs538369264	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63796992	CCTTTCCATCATGGC[C/T]GGAACTAGTTTATCA	8925
rs538370908	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63790145	GAGGGCTACATGATA[C/T]AACACATATAAAGTT	8925
rs538417168	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63676053	GGATTACAGGCGCAC[A/G]CCACTACGGCTGGCT	8925
rs538435814	snp	A/G	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63780448	AACAGAAGGCCGGGC[A/G]CGGTGGCTCATACCT	8925
rs538436252	snp	A/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63814830	CTGCTGTGGAAAATA[A/T]GAAACCTACCTGTCT	8925
rs538436973	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63778547	AGGGTAAAAGAAGAA[A/G]AAGGGGAAATATTTA	8925
rs538442368	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63679839	GTCTTGTAGTTCTTG[A/T]GACTGCACGTTTGAA	8925
rs538461561	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63773272	AACATGGTGAAACCC[C/T]GTCTCTACTAAAAGT	8925
rs538479309	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63639067	ATGTGGAGGACCCCA[C/T]ACCCCTGTAAACTCT	8925
rs538480782	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63817156	AAAGATTTAAAATGA[C/T]GTAATAAACATGCCA	8925
rs538487040	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63718373	CTAAAGTTTCTTAGA[A/C]CCAATATCACACTTG	8925
rs538498177	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63830216	ACTGTGAAGAATACC[A/G]CTAAGGGTTCAAAGT	8925
rs538513257	in-del	-/G			intron-variant	HERC1	GRCh38.p7	15:63734386	ACTCTTTATACAAAC[-/G]ATTTCAGACAAAGTT	8925
rs538526199	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63832916	AAGATGGGTTAGTTT[A/G]TTCAGATTTGTTATT	8925
rs538533699	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63823821	GGAATAATTTAAAAT[A/G]AGAGACATTTCTGCA	8925
rs538546639	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63737071	CTTCAAAAAGTGTAA[C/G]ACAGAACGGGAGGCT	8925
rs538562167	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63691200	GCCGGGCATGGTGAC[C/G]CATGCCTGTAATCCC	8925
rs538568287	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63784457	AAAGGGTTTAATAAT[A/G]AATGCTGAAAACATT	8925
rs538575248	in-del	-/ATATAACTATGCAGTCCCGT	0.442113	0.159977	intron-variant	HERC1	GRCh38.p7	15:63637778	GAAAGGGAAGAGTTG[-/ATATAACTATGCAGTCCCGT]AACTCCTTGATGACT	8925
rs538575604	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63731551	TCTTATCCATTTGCA[A/G]CCATTACTCCTTAAC	8925
rs538582508	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63750130	ATACCATCTTAAAAC[A/T]TCTCCTTTATGTGTT	8925
rs538592792	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63742990	GTAATACTGGCCTCA[C/T]AAAATATAGTTGGGA	8925
rs538599722	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63800888	TTGCCAGAGAAACCA[A/C]CCAAGTGATAAAAGT	8925
rs538615442	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63807433	CCACTAGCTTGGCTT[C/T]CATTGCTCCAGCTCT	8925
rs538619766	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63658287	TCAACAGCCTTAGTT[C/T]CCCATTTCAAGCAAC	8925
rs538633757	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63802701	TAGAAAACTACCAAG[A/G]AACTGGAAAAAAACC	8925
rs538637753	snp	G/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63766672	ATTAAAGGTTAGGGG[G/T]TTTTTTGTTTTGTTT	8925
rs538643300	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63628904	TAGATGGTGGCAGAC[A/T]TAAATAAGTTAATAA	8925
rs538658322	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63665053	AAATGAAAAATAAAG[A/T]TTTAAAGTCATAAGA	8925
rs538661726	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63832289	TGTGTGTGTGTGTGT[C/G]TCTATACATATATAC	8925
rs538672988	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63692260	CTTCTGAAATTAGAG[C/T]TTTCTTTTGATCAAA	8925
rs538692174	snp	A/C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63699255	AGCGCTTTAGCAACA[A/C/T]GCTGCCACAAGAAAA	8925
rs538700593	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63765898	TTTCGCTCTTGTCAC[C/G]CAGGCTGGAGTGCAA	8925
rs538728882	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63706525	AAAATACATGACAAA[C/T]GAGAAAATAACTGAT	8925
rs538767795	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63800042	GGGAGGCTGAGGCAG[A/G]AGGATCCCTTGAGCC	8925
rs538778409	snp	C/T	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63631089	GTTTAAATGATCCTC[C/T]TACCTCAGCCTCCTG	8925
rs538795365	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63805642	AATTATACCTCATCA[A/G]AGCTGACCAAAAACA	8925
rs538805627	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63774246	CTCTACTAGGCTGTT[A/G]GCTCCATGGGGGTGG	8925
rs538807562	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63652082	AACTGTTGAAAATGC[C/T]ACATTCTGATACGGA	8925
rs538816821	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63746858	TGAATATATTGTATA[A/G]CTAAAATCTCAGAGA	8925
rs538838164	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63695489	CTCCCGGGTTCAAGC[A/G]ATTCTCCCTGCCTCA	8925
rs538849461	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63678901	AAGTCTTAGCTTTTC[A/G]TTTAAAACCTGACAC	8925
rs538858886	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63714696	TGGTATTACAGATGC[A/G]CGCCACCACACCGGC	8925
rs538859551	snp	A/C/T	0.000149409	0.00864187	missense	HERC1	GRCh38.p7	15:63630599	TGCGGTCGATTGTGA[A/C/T]TGCGAGCACGCCCCT	8925
rs538860400	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63686288	CAGTCTTTCTACACA[C/T]TTATTATAAGAACCT	8925
rs538874714	snp	C/T	3.44329e-05	0.00414913	intron-variant	HERC1	GRCh38.p7	15:63694679	CTATAAGTTTATCTA[C/T]TAATGTTAAACACAA	8925
rs538885688	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63820436	GATGCTTCTAAATTT[C/T]ATTAACATTGAAATA	8925
rs538890872	in-del	-/AG	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63821975	AAAAAAAGTAAAGCA[-/AG]AGAGATAGGGGATGT	8925
rs538896823	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834756	TTGTTGAGTGAATAC[C/T]CCATCTCCATCTTCC	8925
rs538923599	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63706289	TGTAAGAGATAAAGC[A/C]TCTCTTACATGCTTT	8925
rs538926671	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63751485	TAATACTGTCACTCA[A/G]TAAGGCCTACATAGA	8925
rs538943638	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63819840	TCTGAATTCTCATCC[A/T]GTCTGCATCACTTTC	8925
rs538945592	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63826393	TGGTCCAAATAACTA[C/T]CATACCATGGGTATC	8925
rs538948841	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63736520	CCCTAAAATATAGCC[C/T]AGTCACATCAATCTA	8925
rs538974505	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63794840	GGAGGCCGAGGTGGG[C/T]GGATCACCTGAGGTC	8925
rs538980840	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63658964	TATTTATACTTAATT[G/T]ACCAGTAAGTATTTT	8925
rs538984862	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63686896	AATGATGAGAAGGCA[C/G]TAAGCAGCTGGTCAA	8925
rs539011250	snp	A/C	0.00119737	0.0244387	intron-variant, downstream-variant-500B	HERC1	GRCh38.p7	15:63668876	AAGTAGACAAAAAAA[A/C]CAGAAAGGATAAAGA	8925
rs539011720	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63758831	CCTACCTAGTCTTCA[C/T]GATTGAATAGATAAT	8925
rs539021226	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63610878	GAGTGGGGATGGAGA[A/C]AGAGGGAGGAGAGGC	8925
rs539033875	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63769442	AACAGGGCTAAAGCT[G/T]GGCATTTTTAGAGAA	8925
rs539048903	snp	A/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63750777	TCTCCACAAAAATTT[A/T]AAAAAATTGGTCAAG	8925
rs539049489	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63762755	TGCTCTTCCCATATA[A/G]ACTGTAGCAGAGTAA	8925
rs539064338	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63767868	GTCCATGTGAATGAC[C/T]TTCACACCACTCTCC	8925
rs539066968	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63707851	GGAGAATCACTTGAA[C/T]CCAGGAGGCGGAGGT	8925
rs539071922	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63766518	GCTTGAACCCAGGAG[A/G]CGGAGGTTGCAGATC	8925
rs539080872	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63617441	GGTTCCAAGTCTTTC[C/T]TATTATGAATAGTGC	8925
rs539100103	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63711199	AAATGGTGGCACATG[A/C]CTGTAATCTCAGCTA	8925
rs539115707	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63715087	GTCATTGGTGTTTGG[C/G]GCAGACCTGCTTCTA	8925
rs539119723	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63699194	AAATTAGAGCAATGT[A/T]AGAAAATAAAGGGAA	8925
rs539121928	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63661048	AAACATGAAGAACAT[C/T]GCATTTTTATATAAA	8925
rs539149467	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63740065	ACAGGCATGCGCCAC[C/T]AGACTCAACTAATTT	8925
rs539149817	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63722442	CATAGCACGGAATAT[A/C]ACAGTCTCCCTTATC	8925
rs539179694	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63810019	TAAACTGGTTAAATA[A/C]ATTATACACATATAC	8925
rs539182909	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63627035	GGCCCCAGAGCTTGA[A/G]CCTTTACCTGTCACA	8925
rs539187694	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63675208	GACAAAATAAGGTGC[A/C]TCATGTACACAATAC	8925
rs539188035	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63788323	GTTATTTACTGTAAA[C/T]TGGAGAATTGGGATA	8925
rs539196848	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63738250	TGAAATGTCAAGCTC[A/G]TGAAAGACAAAGAAA	8925
rs539205621	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63768652	TTCTAGGAGCTGGCA[A/C]CAGGGCCATCATGAT	8925
rs539214683	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834180	TTGCTACCGCGCGGC[A/C]CTCACCCTTCAGCCG	8925
rs539223133	snp	C/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63781132	TAATCACTAATAAAA[C/G]TGTCACAAACAGTTT	8925
rs539236817	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63698415	GAGAGCGAAACTCCG[C/T]CTCCAAAAAAAAAAA	8925
rs539259979	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63784667	GGCTGGAGTGCAGTG[C/G]CGCAATCTCGGCTCA	8925
rs539275458	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63697976	TGGGGGAAGATACTT[C/T]AAGGCTATGCAAACA	8925
rs539287495	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63830306	GAAGGACACAACATC[A/G]CTTCTGTAGTTTTCT	8925
rs539295867	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63609867	CATTTAAAATGATAA[C/T]TATGATGACTGGCAG	8925
rs539322589	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63701040	GGGGGGTGTTTTTTT[C/T]TAAATATTAAAATTT	8925
rs539340356	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63744403	CAGCCAGTGGCAAAG[A/C]CAGCCAGGCCGTGTC	8925
rs539378771	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63798154	AACCCCAGAATCAGT[A/G]CTTTAGGATAAAATT	8925
rs539379015	in-del	-/AC	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63706360	TTTCAACGTGTGTGT[-/AC]ACACGTGTACGGGGT	8925
rs539400872	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63796557	GAAAGTTTATTTTGC[C/T]AAGGTTAAGGACATG	8925
rs539425063	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63621400	CTTTGTGGGTAACCC[A/G]ACCTTTCTCTCTGGC	8925
rs539440779	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63763182	ACTTTGTCACCCCCA[C/T]GACCTGGTGTTGGGT	8925
rs539445905	in-del	-/CTGATA	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63623229	TTTACTGGAAAAATC[-/CTGATA]CTAGGTAATGCTGGA	8925
rs539473860	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63784893	TGGGATTACAGGCGT[A/G]AGCCTCTGCCCCTGG	8925
rs539484151	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63730178	AAAAAAAAGCAGCTG[G/T]GTGCGGTAGCTCACA	8925
rs539489755	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63620709	TATATTTAGGATAGT[C/T]AGTTCTTCTTGTTGA	8925
rs539497826	snp	A/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63818172	AGTATTATTTATTTT[A/T]AAATTTTTTTTATTA	8925
rs539511206	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63684164	GAGATTGTATTCTCA[A/G]TACCCTCTAGGTGAT	8925
rs539541742	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63817087	GGAAACTTATCAGGG[C/T]AAACAACCTGCTTTC	8925
rs539543671	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63634530	GGGTTACATTTGTTG[A/G]TTTGTCACATAAACA	8925
rs539566801	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63649254	GCTACTTGGGAGGCT[G/T]AGGCAGGAGAATAGC	8925
rs539575059	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63733579	ATCTGTAGGCTGGGC[A/G]CAGTGGCTCACACCT	8925
rs539645760	snp	A/G	0.000104161	0.00721594	intron-variant	HERC1	GRCh38.p7	15:63747114	CGTCTATGAATTCTC[A/G]GATCATAAAAGTGCC	8925
rs539669411	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63638853	CACAAAGTCCTCTTC[C/T]AATCATTAAGTCTTA	8925
rs539680261	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63754964	TTATAAACTTCAGGA[A/T]CATGATGGTATTGCT	8925
rs539689480	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63615504	AGTCCCAGCTACTGG[A/G]GAGGCTGAGGCCAGA	8925
rs539692847	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63622505	GACCGGCTAATTTTT[A/G]CATTTTTAGTAGAGA	8925
rs539696795	snp	A/G	0.00290311	0.0379885	intron-variant	HERC1	GRCh38.p7	15:63764083	TAATACAAAAGCCAC[A/G]ATTATTACGTACCTC	8925
rs539712697	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63655264	GAGGCTGAGGCAGGA[C/G]AATCACTTGAGCCCA	8925
rs539722721	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63711533	GAAACGTAAAGACAC[C/T]GTTCAACTTTCCTTA	8925
rs539726510	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63818916	ATTAAAATATTGGTT[G/T]AAAAGATATTATAGT	8925
rs539751238	snp	G/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63661526	ATTACTTGCCAACAA[G/T]TCAGAGGTTAACACA	8925
rs539763015	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63719975	ATAAAAGTATATACT[A/G]TGAATACAAGTACAT	8925
rs539805751	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63676867	TGAACAGTTACATAA[C/T]ATCACCAATAAATCC	8925
rs539845310	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63684681	TTTTTCAGAACTGTT[A/C]CTAAAAGTTCTCTAC	8925
rs539850646	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63778972	AAGGAAGAAAGAAAG[A/G]GAAAGAGGTAATTGA	8925
rs539852601	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63692952	TTGGGAGGTCGAGGC[A/G]GGCGGATCACTTGAG	8925
rs539856761	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63770354	TCCCAGTACAGACTT[C/G]TACTATAGCCCATTA	8925
rs539857075	snp	C/T	0	0	intron-variant	HERC1	GRCh38.p7	15:63766245	TTTGATTAATACTAA[C/T]TTATTTATGTTATAT	8925
rs539878656	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63623462	TGCCATTGTTATTCT[C/G]CCAATATTATAACAC	8925
rs539906319	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63637005	AAAAAAACCGTCGGT[A/G]CTCTCTTTGTAGGCT	8925
rs539910447	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63734328	AAAATGGAAAGAAAA[A/G]TATACTCATATTATC	8925
rs539924034	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63832535	ATCATAGTTTCTTTC[A/C]CTTCTACAAATACTG	8925
rs539934125	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63730107	TAACCCTTATGATAC[C/T]AGCTATTAGATGGTA	8925
rs539942318	in-del	-/AAC	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63778054	CCAAAATTTAAGAAA[-/AAC]AAGAAGGAAAAATTA	8925
rs539949852	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63630798	AGGTACACCACGTTC[C/T]GAATAAATAAAAAGT	8925
rs539965636	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63741330	CCGCGCCGGGCCCAT[C/T]TTTTTTTTTTTGAGA	8925
rs539969838	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63729747	CATTATATGGGCTGG[A/G]TGCGGTGACTCACAC	8925
rs539982756	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63805545	GATGAAAAGAGACTA[C/T]ATGATGATTGTGGTG	8925
rs539987692	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63663615	ACATGCCACCATACC[C/T]AGCTAACCGTTTTTT	8925
rs540009394	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63764372	GAAGTTTTATTAAAC[A/G]AGCTGGCTACTGCAT	8925
rs540020022	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63808916	TCATGACAATCAACA[-/T]TTTTTAGTAAATTTA	8925
rs540020213	in-del	-/AA			intron-variant	HERC1	GRCh38.p7	15:63829479	ATATATGTTTATATA[-/AA]TATATATATATATAT	8925
rs540030192	in-del	-/AAC	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63762242	AATAGCCAAAAATGA[-/AAC]AACATGACCTTCACT	8925
rs540046934	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63662716	GTAATTTATCTTTGA[A/C]ATCAGAATCAAATAT	8925
rs540048260	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63736484	AAAGACTTTAAGTGA[C/T]AGACATGAAATATTA	8925
rs540052974	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63670470	AATACAATGGTATAC[A/C]CACAGGAAGGAGTAG	8925
rs540058420	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63658496	AGACTTCCAGCTAAT[A/G]TACACTAGAAGTTAA	8925
rs540064494	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63741065	ACGGACTCTTGCCCT[C/G]TCGCCCAGGCTGGAG	8925
rs540080309	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63755660	TGGCGCATGTCTATA[A/G]TCCCAGCTACTCAGA	8925
rs540092092	snp	A/G	0.00597247	0.0543191	intron-variant	HERC1	GRCh38.p7	15:63699758	GTATTTTTTAAGCTA[A/G]AATCTTTACATTAGA	8925
rs540116617	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63611731	TTGTAGTATGCTCTC[C/T]TCATCCACTTAGGAC	8925
rs540128058	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63724411	AATGATGAATGTACA[C/T]TCATATTTGGAAATG	8925
rs540146786	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63629093	TGGCTGAGATTACAG[A/G]TGCCCGCCACCACAC	8925
rs540162004	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63624442	TGGCTCATGCCTGTA[A/G]TCCCAGCACTTTGGG	8925
rs540162102	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63617150	TATCTCCTAATGCTA[C/T]CCCTCCCCGCTCCCC	8925
rs540171288	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63715459	CCTTCCCCATCTCCA[A/C]CTCCCTTTACTCCAT	8925
rs540176824	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63714697	GGTATTACAGATGCG[C/T]GCCACCACACCGGCT	8925
rs540209966	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63759273	CTGTTCTAAAAACAG[C/T]GAAGGCACAAAGCAA	8925
rs540213016	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63759343	TCATGGCTTATTTAC[C/G]ATTTCTGTAGAATAT	8925
rs540217300	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63640010	TTGAAAGTGACTATC[G/T]GAAAGAAAAATATTT	8925
rs540225578	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63731263	TATGTGTACAATATA[C/T]AAGACAATATGAGAA	8925
rs540232012	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63688790	GTGACTATATGCATG[A/G]GGACATTATGATAAT	8925
rs540234746	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63774478	CAAAGCTAAAACTAT[A/G]AACCTGACTTCTGAT	8925
rs540240001	in-del	-/CAGGCACG			intron-variant	HERC1	GRCh38.p7	15:63649076	CAATTTCATCTCGGC[-/CAGGCACG]GTGGCTCACGCCTGT	8925
rs540304696	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63687416	GGTGGCAGGTGCCTG[C/T]AATCCCAGCTACTTA	8925
rs540324649	in-del	-/CC	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63644156	CTCTCCACCCTTTCT[-/CC]CCCCATCCTTAAGCT	8925
rs540325470	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834333	CGTGGTGGGCAGGGA[A/G]GACCCCGCCGCCAGG	8925
rs540327557	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63779991	TGCACTCCAGCCTGG[C/T]GACAGAGGGAGACTC	8925
rs540330532	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63813430	TCTTCTTAATGTTTA[C/T]AAAATCTGAGTTACT	8925
rs540363508	snp	C/T	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63780565	TTTCTACTAAAAATA[C/T]AAAAAAATTAGCTGG	8925
rs540364624	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63794944	GGTGGTGTGTACCTG[C/T]AGTCCCAGCTACTCA	8925
rs540377238	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63794300	TTTCTTGCGTGAGAT[A/C]CAAGAACCCTCTCCT	8925
rs540388979	snp	A/C/G	0.000341757	0.0130678	intron-variant	HERC1	GRCh38.p7	15:63729378	TGAGTTCTAAGAAGA[A/C/G]AAAAAGTTCCTAAAT	8925
rs540395501	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63712704	AACATATTACTTACT[C/T]TAACCAAAGCCTTAC	8925
rs540407272	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63759950	ATAAAAGGTCTGGAA[C/T]TTTGCTGGAGATAAA	8925
rs540448426	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63673764	GAGTCTCGCTCAGCC[A/G]CCCAGGCTTGAGTGC	8925
rs540461239	snp	A/C	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63708921	ATCTGCTTTCTCTCT[A/C]GTTCTTGTCTTTTCC	8925
rs540484119	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63761245	AGTATTGAGCATTAA[A/G]TAAGTAATCATTTGT	8925
rs540485102	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63673336	TCACAATCATCATGA[C/T]CTTAACATTCCTACT	8925
rs540518686	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63808605	AATATACTTTTTAAC[A/G]AAAGGATCTTTGGGG	8925
rs540540420	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63640800	TCTAAGCTATCACAC[C/T]GCATATAGTACATTT	8925
rs540552351	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63807495	CTCAGACTTAAAAGT[C/G]TACTAATGGCTTCCC	8925
rs540556963	in-del	-/TA	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63677630	ACAGAACAAAAAGAC[-/TA]TGTATTTTTAAAACC	8925
rs540577809	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63632054	TTCTCAATAGCCTAG[C/T]GGACATTTCCACACA	8925
rs540583302	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63784890	TGCTGGGATTACAGG[C/T]GTGAGCCTCTGCCCC	8925
rs540584545	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63739136	AAAAGAAAAAAAGCC[A/G]TGTGCCCATTACCAG	8925
rs540588225	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63789239	GGGACTACAGGCGCC[C/T]GCCACTACGCCCGGC	8925
rs540615546	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834883	GGGGACAAAAAATAG[A/C]GTTGGCCTCTGCGTT	8925
rs540621634	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63688094	GAGAATGGACTTTAG[G/T]GCATAACAATGGAAG	8925
rs540631191	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63827614	AACATACAGTAATCA[C/T]ATGACCCAGCAATTC	8925
rs540659006	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63691403	CCTGGAAGTGAGAGG[C/T]TGCAGTGAGTTGAGA	8925
rs540667668	snp	A/C	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63821668	GGAGGTCAAGGCTGT[A/C]ATGAGCCATGATCCC	8925
rs540667680	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63828277	AGAGGTAGAAACAAA[C/G]ATGGAGGGATGGAAA	8925
rs540702045	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63824224	CATTATGGAAAACAG[C/T]ATGTAGGTTTCTCAA	8925
rs540715140	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63649134	CCAAGGTGGGCGGAT[A/C]ACAAGGTGAGGAGAT	8925
rs540723417	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	HERC1, FBXL22	GRCh38.p7	15:63608647	CTGCTTTATTTCTCT[A/G]CATAAGGAACCCTGA	8925
rs540730522	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63702248	AGAAATTTGATACAG[C/G]AGAGAAACATTTACA	8925
rs540784408	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63615221	CCAGATGAAAACAGT[C/T]TCAATCCAACCAAAG	8925
rs540785690	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63717159	CTCATGACCATTAAA[C/T]AATTTAAGACTTTTA	8925
rs540802063	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63680470	CTGAATACGTGGCAC[C/T]TGAATAACCGAGTTG	8925
rs540803651	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63670242	GTCAGCGGCACAGTC[A/G]GGGAAAGGTACGGGG	8925
rs540815136	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63677192	GGATTTTGGATTTTT[G/T]GATTTGGGATGCTCA	8925
rs540832974	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63768129	ATAGCACATTGCTCA[C/T]CGTCTTCAGATCTCT	8925
rs540840197	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63677162	GCTCAATGGAAATAT[G/T]CATTGGAGCACTTTG	8925
rs540855524	snp	A/C	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63626461	TAGGCAGTTCTTTCA[A/C]AAAAATAAAGCCAAA	8925
rs540867852	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63815900	ATGGGGGCAAGAAGG[A/C]GAAGTGCCTAGCAAA	8925
rs540874566	snp	C/T	7.42914e-05	0.00609428	intron-variant	HERC1	GRCh38.p7	15:63690514	CAAATATGGAAAACA[C/T]CTTCTAATAATTTTA	8925
rs540880649	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63771616	TTTTTATTTTTAATA[C/G]AGACAGGGTTTCACC	8925
rs540880993	snp	A/C/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63676479	GATATTGTTCCGGCC[A/C/G]AGCGTGGTGGCTCAT	8925
rs540882341	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63681970	ATGAGTGTATCAACG[C/T]GTGGAGTCTGACGAG	8925
rs540898028	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63647210	AGTGAGCCAAGATCG[C/T]GCCACTGCACTCCAG	8925
rs540902263	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63822094	AATTATGTGAGCGAG[C/T]CAGCAGTGCAAAAAC	8925
rs540921430	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63684870	AAAAATTAGCCAGGC[A/G]TGGTGGCAGGCGCCT	8925
rs540922186	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63777473	GCCAGTTTGATAGCT[A/G]TACAGGGATACGTTG	8925
rs540924567	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63625817	ATCATGTCCAACCTC[A/T]AGACTGTCCCTAACA	8925
rs540938022	in-del	-/G			intron-variant	HERC1	GRCh38.p7	15:63684960	GTTGCAGTGAGCCAA[-/G]ATCGCACCACTGCAC	8925
rs540953407	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63723535	TCAACCCTTTTACAT[C/T]CTCCAAAAGGATGTG	8925
rs540959074	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63778378	AGACTACAGGGAAGA[C/G]ATTTTAAAGTACATT	8925
rs540974181	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63643180	AGCTAAATTCAGCAA[C/T]GTCCAATCACATACC	8925
rs541009119	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63684247	ATCAATTGACTCTAC[A/G]TCCCTCACCTTTCTC	8925
rs541026728	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63830462	GAACTGTCAGAGATT[C/G]GAGGAAATGAAGAAG	8925
rs541029383	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63645354	TGAGGTAATCTTATA[A/G]TGTTACACATTATAA	8925
rs541038465	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63707211	ATTACTACTCCTTCC[A/T]CTAGCTTCACTTTCT	8925
rs541047791	snp	C/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63690903	GTGCCAGATACTATG[C/G]TATGCTACACATTTC	8925
rs541050549	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63609683	GTAGAATGGAAAGAA[C/T]GACTGTGAGGTGCAG	8925
rs541060346	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63711787	AATCGAGACCAGAAG[C/T]CAAGTCTGACACATC	8925
rs541072785	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63663624	CATACCCAGCTAACC[A/G]TTTTTTAATTTTTTT	8925
rs541088629	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63688177	GCTTGGAATAGGGTG[A/T]TGACAGAAGAGATGA	8925
rs541100649	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63698214	TGAGGTCAGAAGCTC[C/G]AGACCAGCCTGGCCA	8925
rs541102020	snp	A/T	0.00874735	0.0655527	intron-variant	HERC1	GRCh38.p7	15:63706285	TTCATGTAAGAGATA[A/T]AGCATCTCTTACATG	8925
rs541113741	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63616219	GCAGAAAAAAATTAA[C/G]GGGGAAGGAGCAACT	8925
rs541139360	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63705188	GACAGGGTCTCACTG[C/T]TGTCACACAGGCTGG	8925
rs541139820	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63791627	TGAAAGTAAAAAACA[A/G]TTCTTCGAGGGAGTT	8925
rs541160980	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63684652	GGAGGAGTCGGGAGG[A/G]CATTAATGATCTGTT	8925
rs541162288	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63747202	CGGTGGCTCATGCCT[C/G]TAATCCCAGCACTTT	8925
rs541165294	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63670920	AAAAAATTAGCGAGG[A/G]GCCAGGTGCGGTGGC	8925
rs541183341	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63799217	AACAAAAAGTAGCTA[C/T]TGGCCAGGCACAGTG	8925
rs541215709	snp	G/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63764594	ACCTGACAGAATACA[G/T]CCAGCTTTAGTAATG	8925
rs541224085	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63787067	GGCTGGTCTTGAAGT[C/T]CTGACCTCAAGTGAT	8925
rs541225609	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63825729	TTTTCCTGGGAACAT[C/T]AGTTCATTAGAAAAC	8925
rs541232440	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63736742	GCCTTAAGTAGCTGG[A/G]ATTACAGGCATGCGC	8925
rs541232823	snp	C/T	0.00011606	0.00761685	intron-variant	HERC1	GRCh38.p7	15:63764209	ATAATTAAAACATTG[C/T]GGGACACAGCGTAGG	8925
rs541238171	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63827018	AAGATACGGTTCTAA[C/T]GATACCAAAATACTA	8925
rs541242308	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63782497	AAAAAGCTTCCTTTC[A/G]AAACATTACTGTTCA	8925
rs541251983	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63826048	AACTAACAGGTGTGA[A/G]CCACCACGCCCGGCC	8925
rs541254022	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63686021	GTGGGCACTGAATCT[C/T]TAATGGGCTTTCCTA	8925
rs541264046	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63629277	ATACATTCTGATTTT[C/G]TTTATCATAACAGTC	8925
rs541283815	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63831847	AAGCAGATTAAGTGA[C/T]GCATTTACATTTGCT	8925
rs541290884	snp	A/T	0.00597247	0.0543191	intron-variant	HERC1	GRCh38.p7	15:63824611	TTAACCCAAAAGAAA[A/T]AAAAGCAGCACCTCT	8925
rs541300524	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63700184	AAAAAAGAGTATCAT[C/T]TTATATCACCTTTTT	8925
rs541301015	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63693040	ACAAAAATTAGATGG[A/G]TGTGGTGGCACACGC	8925
rs541303587	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63664106	CCAGGGCCTACTTTT[C/T]TGGCACAGTGCCCTT	8925
rs541308678	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63800353	TCTCTCTTCTATAGA[C/T]GCCTGAGATCCTTAA	8925
rs541311990	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63635045	AAAATTTTTTTTTTT[A/G]ATTTTTTTTTAAATT	8925
rs541324360	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63727528	TTTTAAGATTTCAGT[A/G]ATGAAATTCCTTTGA	8925
rs541324775	in-del	-/A	0.00874735	0.0655527	intron-variant	HERC1	GRCh38.p7	15:63776784	CCGCCTGGACAACAC[-/A]GTGAGATCTCGTCTC	8925
rs541328894	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63636426	CAGGCATGTGCCACC[A/G]TATCTGGCTAATTTT	8925
rs541345996	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63771893	GGAAATCCAGCAGTT[-/A]AAAAAAAAAATTATT	8925
rs541348291	snp	A/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63693089	AGGCTGAGGCAGCAC[A/T]ATCGCTTGAACCTGG	8925
rs541400400	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63686006	TTCCCTATAAAAATT[A/G]TGGGCACTGAATCTC	8925
rs541405451	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63629338	GCAACAAGGCCATTC[C/T]AAATCTAGCAGATGA	8925
rs541421441	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63656483	GCTGCACTATCATTA[C/G]CCATACATGTCCTAA	8925
rs541422496	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63757175	AATCAAATAGAAAGT[C/T]CTAGCTGGGCTACAA	8925
rs541428915	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63668000	ATATACAGATTTTCA[A/G]CTGTTCAGGGGGTTG	8925
rs541437008	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63706994	CCCTAAAAACCCACT[A/G]AACATAGCTATAAGG	8925
rs541444054	in-del	-/A	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63805445	AAAAACCACGGTGAT[-/A]AAAAAGCACATCAGT	8925
rs541461960	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609313	GACATCAGAGTGCCA[C/T]AAGGGGGAGTGGGGC	8925
rs541473873	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63702549	AGTATCTGCAAAAAC[A/G]TATTGTCTTTCTGTA	8925
rs541476504	snp	G/T	5.62414e-05	0.0053026	intron-variant	HERC1	GRCh38.p7	15:63615721	CAGCTCTCATTTGGA[G/T]AGAAACCCAAGCATT	8925
rs541492349	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63807797	TCCTACCTTTGTGCC[C/T]CCACTCATGCTGTTG	8925
rs541502597	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63644071	AAAGAGTAAACCAGA[C/T]CTATCTGTAGTACTC	8925
rs541529078	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63808565	TGCTGGAATTACAGG[C/T]GTGAGCCACTGTACA	8925
rs541529801	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63712670	TTATTTTTGAAAAAA[A/T]TTTTATATGTCTAAA	8925
rs541549356	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63628612	TGGGAACTGGCAAGC[A/G]GACAGTGCCATGGGG	8925
rs541561153	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63622240	ATAAATCAGGTTTCA[C/T]GATTAAGTCTGAGCT	8925
rs541566305	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63673728	CAGAATACTATGTAT[C/T]TTGGTTTGTTTTTTG	8925
rs541583356	snp	C/T	0.000447431	0.0149504	missense	HERC1	GRCh38.p7	15:63716328	ATCACTTCATGTTCC[C/T]GTTCCTCCTCTTCAT	8925
rs541589685	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63681243	GTCTCACTCTGTTTC[C/T]CAGGCTGGAGTACAG	8925
rs541591825	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63645297	GATAAGGAGATTACA[A/T]ACCAAGTTTCACACT	8925
rs541592677	in-del	-/AA	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63644056	GCTGCCCTCCAGCAC[-/AA]AGAGTAAACCAGACC	8925
rs541615336	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63735836	ATCCAAAAGCATGTG[C/T]CCTCCAACACAGTTA	8925
rs541620961	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63828449	GGTTCAAGTGATTCT[C/T]CTGCCTCAGACTCTT	8925
rs541621257	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835405	TATGATCTGGGTATT[A/G]TGTGTGAAGCATACT	8925
rs541621840	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63626858	ACTGAGTACCTTCTA[C/T]GTGCCTGGCACTATT	8925
rs541642039	in-del	-/AGTA	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63629660	ATTAACTCTCCTCTC[-/AGTA]AGAGTGCAACCACAA	8925
rs541646399	snp	A/C	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63685534	ACATTTTAAAAGTTA[A/C]GACAAAAGCTTAAGA	8925
rs541660255	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63824090	CAAAACCACAATGAG[G/T]TATCACCTGACACCT	8925
rs541681553	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835010	CGAGGGAGTGCTTTC[C/T]CATGGTTAAATTAGA	8925
rs541686071	snp	A/C	1.66352e-05	0.00288398	missense	HERC1	GRCh38.p7	15:63692497	ATTGCTTTTGAAGAT[A/C]CAACTCTGCGAAGAA	8925
rs541704971	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63749946	TAAAGATTGTTACAG[C/T]GATTTATCATGCTGC	8925
rs541707539	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63813226	GTGGTTTCTCAAGAA[C/T]TGACTTCAAGTACAA	8925
rs541732051	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63695993	AGGAAATGGAACCAA[G/T]GAGCTATCTTAAAAA	8925
rs541732340	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63702933	ACATGGTGAAACTCC[A/G]TCTCTACTAAAAATA	8925
rs541735548	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63650841	AATACTAATAAGCTC[A/G]ATATTACAATAATTA	8925
rs541737506	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63644738	GACTCGTCTATCTGT[A/G]GTATCAATTATATCC	8925
rs541742225	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63795911	TAACTTGTGGAATGC[C/T]GAGAAAGGTAAAAAT	8925
rs541749557	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63742308	GTTGGTGTATAGAAA[C/T]AATTTTTGTACATTT	8925
rs541774667	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63650277	CAGGCATGGTGGCAC[A/G]CGCCTGTAGTCCCAG	8925
rs541779685	snp	G/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63725924	ATGCTTTTTAAGGCC[G/T]GAATTCAGAATTGTC	8925
rs541801312	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63745456	GATCAGCAGTTCCCC[C/T]CTGGCTAGGGTTGGT	8925
rs541809234	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63652725	TGGCTCAATCTCAGC[C/T]CACTGCAACCTCCAT	8925
rs541814594	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63699319	TTAAAATGCTCTGCA[A/G]TATTAAACCAGATCA	8925
rs541814610	snp	A/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63717744	GGGCGTGGTGGTGCA[A/T]GCCTGTAATCCCAGC	8925
rs541832163	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63768242	TTAGGATGTTGCTTC[C/T]CAAATTTCAATGTTG	8925
rs541832529	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63762476	TTACAGACGTCTGCC[A/G]CCCCACCCAGCTAAT	8925
rs541835285	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63618969	GACTTCCTCTTTTCC[C/T]AACTGAATGCCCTTT	8925
rs541857251	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63627219	CTCTCTTAGATATCT[A/G]AGAAACAAAATCCCT	8925
rs541865114	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63671060	TACAAAAAGTTAGCC[A/G]GGAGTGGTAGCACAT	8925
rs541866337	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63752583	CTAAGTGTTCTCTTT[A/C]CCCTCCTTTTTGATC	8925
rs541916870	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63801813	TCAGTCTCCTCCTCT[C/T]CATGTACATACATTT	8925
rs541946219	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63625707	TCAAAAAAAAAAAAA[A/G]AAAGAAAGAAATGGT	8925
rs541949162	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63732257	CCACCCAACTCGGCC[C/T]CCCAAAGTGCTGAGA	8925
rs541976083	snp	A/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63739638	GAGGTAAGGAGTTCA[A/T]GACCAGCCTGGCCAA	8925
rs541997288	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63647835	GGCAAGAAAGTGGTG[A/G]AAAGGGAACTCACGT	8925
rs542002543	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63754432	TCTACACTAGGCATA[C/T]ATAACTGAAAAATAA	8925
rs542013211	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63745936	CATTTTTCTTGGTCA[A/G]TCCAGCCAGAGGTTT	8925
rs542020445	snp	C/G	1.65743e-05	0.00287869	missense	HERC1	GRCh38.p7	15:63661770	TTCAGAACTTGTTGA[C/G]TTAGATTTGGTCTTC	8925
rs542036526	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63746870	ATAGCTAAAATCTCA[C/G]AGAAAGACGTGGTTT	8925
rs542103825	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63797697	AATTAAACTCTTCCT[C/T]TACTGCAATGTAGTG	8925
rs542105851	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63711689	TACACATGGAGCTTA[C/T]AGATAAGTCCATCTC	8925
rs542106723	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63620903	TCTGCATGTGAGATG[C/G]GTTTCCTGAATGCAG	8925
rs542118850	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63627810	GCCCACAGTTGGGTG[C/T]TGAGCACACAAGTAT	8925
rs542127624	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63796614	GATGACATGTACCCA[A/G]GGTGGTCAGGGACAG	8925
rs542131547	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63788440	GGAAGAATTCTATCA[C/T]GACTTCAACAGACAA	8925
rs542132369	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63647378	GAAAGTGGTGAAAAG[A/G]GAACTCTTAAACACT	8925
rs542134390	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63653800	TCCATTGGTAGTTGG[C/T]TGAATCAATGGATGC	8925
rs542138975	snp	A/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63620016	TGCTCTGATCTTAGT[A/T]ATTTATTGCCTTCTG	8925
rs542164773	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63789386	TGAGCCACCGCGCCC[A/G]GCCAAAAGGTTTTTT	8925
rs542173906	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63710760	AGACTTGAAGAAAGA[C/G]AGGGAGTTAGCCATG	8925
rs542198818	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63823080	TCATGGGGGTTTGTT[A/G]TACAGATTATTTCAT	8925
rs542221686	in-del	-/TAAT			intron-variant	HERC1	GRCh38.p7	15:63660332	TCAAAGAAATAAAAA[-/TAAT]CAATAAATAAATAAA	8925
rs542224258	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63764833	CCTGAAACTTGTGAT[C/T]AGCAACTTGCTAATA	8925
rs542231238	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63779933	GCAGGAGAATCGCTC[A/G]AACCCGGGAGGTGGA	8925
rs542238671	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63816739	CCAGTACCAGTGCTG[A/G]CATACAGTGTCCTAA	8925
rs542251660	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63825999	AACTCCTGACCTCAG[G/T]TGATCCACCCACCTC	8925
rs542252338	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63637203	ACATGCATGATTGCT[A/G]CTGCTATTAACATCT	8925
rs542257530	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63804045	AGGAAAAGGATAATC[G/T]TTTCAACAAAAGGTG	8925
rs542260915	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63820686	ACAGAGACGTTATCC[-/T]TTTTTTTTTGCTTTT	8925
rs542265527	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63783259	CAAACTTCACTGTTG[A/T]CTTGTTTTAATAAAT	8925
rs542266234	snp	C/G/T	0.00159649	0.0282165	intron-variant	HERC1	GRCh38.p7	15:63772911	TTGTAAAACATGACC[C/G/T]AATATTTACCATTTA	8925
rs542287595	in-del	-/AAAAC			intron-variant	HERC1	GRCh38.p7	15:63805957	CAAAACAAAAAAAAA[-/AAAAC]AAACAAAACCCAATT	8925
rs542301454	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63753341	ACTTTAAAAGAAACA[C/T]AGACAATTATTTTTC	8925
rs542322704	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63641779	TATCCAAAAAGGCTA[C/T]GCTTTTAATGCCTAT	8925
rs542348665	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63735707	CTAAGATAAACTCCA[C/T]AGCGCCTGTCAGTTC	8925
rs542352766	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63637424	TTATCTAGCAAAGGT[C/T]TGAGAAGGGCAAAGG	8925
rs542377589	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63657667	CTTTTATGGCAGATT[C/G]CTTTTGTGACTTGCT	8925
rs542392817	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63644639	ATAAATCATTCTTCA[C/T]AGCAAGGATTCTGGC	8925
rs542395927	snp	C/T	4.97211e-05	0.00498579	synonymous-codon	HERC1	GRCh38.p7	15:63758205	GAAACTAGGAGCCAG[C/T]TTGGGTTGCAGTATT	8925
rs542438206	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63755807	AAGAAAAGAGAGGAA[C/G]AGAGAGGAGGGGAGA	8925
rs542482598	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63616941	ATTCTGAACTATTTT[C/T]AGAAGAACTATGTAA	8925
rs542491237	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63704551	TTTATTAATATAACA[C/T]ACAACTTTTAGCAAT	8925
rs542494473	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63711306	AGTGACAGGGTAATA[A/T]CCTGTCTCAAAAAAA	8925
rs542509499	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63810224	TTTGTACACCAATGT[G/T]AATAGGAGCATTATT	8925
rs542546019	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63803846	ACATTAAAGATGTAC[A/T]TTATCTGACTTTTAA	8925
rs542559341	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63765474	CATGCCTCATTATAT[C/G]CATCCAGCGTTAACA	8925
rs542567805	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63721146	ATCAGAAAATACATC[C/T]TAGAAAGTAAACTTT	8925
rs542577188	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63721937	GCAATCTTGACTCAC[G/T]GCAACCTCCACCTCC	8925
rs542593106	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63793883	GCTGCATTCCCAGAC[A/G]GTTAAGGCATTCTAA	8925
rs542597700	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63671705	AGGTGGCCTTGGGCA[A/C]ACCAAAAATTGAGAA	8925
rs542607028	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63765651	CGGCCAATCAGAATA[C/T]GTTTAAATCTACCTA	8925
rs542621279	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63819855	AGTCTGCATCACTTT[C/T]TAGCTGCATGATCTT	8925
rs542623134	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63651891	TAATACAAAAATTAG[A/C]CGGGCATGGTGGCAG	8925
rs542628331	snp	C/T	0.00676609	0.0577691	intron-variant	HERC1	GRCh38.p7	15:63797308	AAGTATAGCTTCTTC[C/T]ATCATTCCTTACTGT	8925
rs542630278	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63645980	TATCTCTCATTAGCA[C/T]TTGTATTTATTAAGA	8925
rs542661706	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63622299	TGGTCTCAATAAATA[A/C]CAAGTCTTGATGGAA	8925
rs542673725	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63812641	GGAACTCATGAAGCT[A/G]CACACTAGTAAGCTT	8925
rs542689693	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63693871	TCCCATCATACCTCA[A/T]AAGGAAGAGGAACTC	8925
rs542694838	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63793858	GTAAAATGAGGCTGA[C/G]ACCTACTGGGCTGCA	8925
rs542701445	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63728786	GGCATGTCCAAGGAA[C/G]AGGAGCCTATAGGAA	8925
rs542729782	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63768936	TGCATTATGTATATA[C/T]ATATTGAGAAAGAAG	8925
rs542746084	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63735535	TGTACCCTAAAATTT[A/G]AAGTATAAAAAAAAA	8925
rs542781808	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63703556	AGGGAAAACATTTTA[C/T]ATTTCCTCCTCAAAA	8925
rs542812318	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63723414	TGGTGCTACAGATAA[A/T]ATCTTACCACATTTA	8925
rs542819078	in-del	-/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63755701	GGGAGGACCACCTGA[-/G]CCCCAGGAAATCAAA	8925
rs542822676	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63774387	ACCTGCTGATCACTA[C/G]CCAAAATCTCTAATT	8925
rs542826290	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63750069	CTGCTAAACCACTAA[A/T]CGGCTTGCAATTTGT	8925
rs542841264	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63740892	TTCATTTTCTTGAAA[A/G]TATCCTTTGAAGCAC	8925
rs542843886	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63814756	TTACAGGCGTGAGCC[A/G]CCACACACGGCCAAC	8925
rs542859252	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63766969	AGGCGTGAGCCACCA[C/T]GCCCAGCCTACACTA	8925
rs542884135	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63806908	ATGCGCCACCGCGCC[C/T]GGCTAAGTTTTATAT	8925
rs542906338	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63827532	AAAAGTGCAAAAGAG[C/T]ATAGTATACTCTCCA	8925
rs542910762	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63813355	ACACACACACAAACT[C/T]GTAAGTACACACACT	8925
rs542913581	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63780653	TGTGAACCCGGGAGG[C/T]GGAGGTTACGGTGAG	8925
rs542923418	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63818477	AGGAAAAAATAACAG[A/G]AAGAACTGAAAGACA	8925
rs542931115	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63714613	GGAGTGCAGTGGCAC[A/G]ATCTCGGCTCACTGC	8925
rs542948460	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63663896	CTGAATCATTACTCA[C/T]GTTATAGTATTTCAG	8925
rs542950257	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63781137	ACTAATAAAACTGTC[A/G]CAAACAGTTTTATTT	8925
rs542988177	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63639476	TTCCCAGCGTCAAGA[C/T]TGCCTAACAATGCAT	8925
rs543013663	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63720055	ATGTAGTTGAAAACC[A/G]AAATCACAACATTAG	8925
rs543021154	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63833619	AGCCGGGGACCCGGG[A/G]GATCCGCGGCGCGCC	8925
rs543025779	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63654739	CATGGTATGGTGGCA[C/T]GTGCCTATAATCCCA	8925
rs543035204	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63786138	GCACTGCAGTGTGCC[A/T]GTAGTCCCAGCTACT	8925
rs543058014	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834263	AAGCACAATTGGGGG[C/T]GTTTCACAAAGGGTG	8925
rs543079674	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63693223	CAGATATCAAAACCC[C/T]TGGTGCTGGGGAATT	8925
rs543095832	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63645425	GCCACACTTAATGCA[A/G]ATAACAGTCTATACC	8925
rs543101329	snp	C/G	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63796807	TAAAGAAAGAAATGT[C/G]TGTGTTACAATAAAG	8925
rs543114624	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63693445	GATGGGGTTCCACCA[C/T]GTTGCCCAGGCTGAT	8925
rs543115281	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63701148	TATTAGAACTGCAGA[A/T]GAAAAAGAGACCTTA	8925
rs543118309	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63700377	AAATTATATCAGTTA[C/T]GTAACTAGATAGAAA	8925
rs543149989	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63721785	ACAATCCCGATCATC[A/G]TTAAAAAAACAAAGG	8925
rs543161340	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63610427	GATGCTGACAACCCT[G/T]AGACCGGAGATTAGT	8925
rs543162230	snp	A/G	1.65726e-05	0.00287855	synonymous-codon	HERC1	GRCh38.p7	15:63660998	ACTGTCTTGCTTGCC[A/G]ATTAGATCTGGAGCT	8925
rs543162491	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63653993	GTAATTGTGTGCATG[C/T]GTATGTGTACGTGTG	8925
rs543195281	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63790586	CGTCTCAAAAAAAAA[-/T]TTTTTTTTTTAAAAA	8925
rs543208815	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63627872	CTATACAAAAATTTC[A/G]TAATAAATTAAAAAT	8925
rs543211163	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63677148	AGCACCAACATGATG[C/T]TCAATGGAAATATTC	8925
rs543240333	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63817571	AATACAAAAATTAGC[C/T]GGGCGGGGCAGCACA	8925
rs543260369	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63687329	CGGATCACAAGGTCA[G/T]TAGTTTGAGATCAGC	8925
rs543268282	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63675682	AATAATGCCTCTATA[A/G]TTTAAGCCAAAATAT	8925
rs543322574	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63651668	CAGATGGTTATTATT[C/G]AGAAGACATTGATTC	8925
rs543324693	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63617458	ATTATGAATAGTGCC[A/G]CAATAAACATACGTG	8925
rs543336643	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63773672	CCTCAGCCTCCCAAG[C/T]AGCTAGGATTACAGG	8925
rs543340926	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63731166	CTTAACCACTCCTCT[A/T]TTTTTAGATGTTTCT	8925
rs543342766	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63646573	TTGGGAGGCCGAGGT[A/G]GGCGGATCATGAAGT	8925
rs543345857	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63726202	GGCCAGGCTGGTCTT[A/G]AACTCCTGACCTCAG	8925
rs543375158	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63738341	ATATGGGATCCCAAA[C/T]AGGATCCTGCAACAA	8925
rs543375567	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63730449	GGGCAACAGAAAGCC[A/T]GTCTCTAATAAAATT	8925
rs543379806	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63648615	ATTCCCTATTCAGTA[C/T]GTTTCCATATTCTAT	8925
rs543386486	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63776742	ACGCCAAGGCAGGAG[A/G]ACTGCTTGAGCTCAG	8925
rs543404670	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63751850	TTATTATTATTACTA[C/T]TATTACTACCACTAC	8925
rs543430899	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63783514	ACATAACCTTTATAT[A/G]CACTGAGAAACCAAA	8925
rs543433543	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63755573	TGTTTGAGCTCAGGA[A/G]TTCGAGTTCAGCCTG	8925
rs543437106	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63697663	TTTCACCACGCTGGT[A/G]AGGCTGGTTTCAAAC	8925
rs543454781	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63712626	CATATGTGGTAAACA[C/T]ATATGCAATATAGTT	8925
rs543455989	snp	A/C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63687305	AGCAATTTGAGAGAC[A/C/G]GAAGCGGGCGGATCA	8925
rs543475013	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63818257	TGTCTTTCTAGTCCT[A/G]TGGGCCTATGGTACT	8925
rs543475257	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63810970	GGCAAATTCACATTG[C/T]AGGACATTGTATAAG	8925
rs543475353	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63704375	CAGACTGAATCTCAA[A/C]TTATATTTCCATATG	8925
rs543487342	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63630100	CTGATGTTCCCAGGA[C/T]CTAATCTCACATCTT	8925
rs543493509	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63711984	TTCTAGATAGTTTTC[A/G]CTTTATATTTTACCA	8925
rs543497132	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63614303	ACTCAGTGCTTTCTT[C/T]TGTGAAACAGAGCTG	8925
rs543513369	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63811597	GGCAGATCACGAGGT[C/T]GGGAGATCGAGACCA	8925
rs543528926	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63691017	GTAACTTGACCAAAG[C/T]CACACAAGCTCATAG	8925
rs543555628	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63804454	AGCCGGGCATGGTGG[C/T]GGGCGCCTGTCATTC	8925
rs543560159	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63613533	TCTGAATAGGGACCA[C/T]ACCTTAAGGAAGTGA	8925
rs543581249	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63742262	TTGTACATAAACTTG[G/T]TTCCTTAATTTCATT	8925
rs543591983	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63824087	AATCAAAACCACAAT[A/G]AGGTATCACCTGACA	8925
rs543592450	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63656724	TTTTCTCAGTCACGA[C/T]GCTCTCAGAAGTAAC	8925
rs543607354	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63628059	TTTATTTCTAACAGT[A/G]GGCCTTAGAAAGCTA	8925
rs543609206	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63636254	AATTGGTACTATGAA[A/G]ATAAGAATAATTTCA	8925
rs543613872	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63803312	CCAAGGTCACAACTG[A/C]CAGTAATTGATAGAG	8925
rs543625983	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63633494	AATAATAAGCAGAAA[C/T]GGCAGCTGCATGCAG	8925
rs543645786	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63769958	CCCTCACATTTGTCT[C/G]CTTAAGATATTCAAA	8925
rs543647165	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63692283	TGATCAAATAGGTAC[A/G]CAGAAAATAAGAAAG	8925
rs543714850	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63706232	TTGTTCCTCATGAAA[C/T]TTTTAAAATATTTTT	8925
rs543718414	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63635126	GATCACAGCTCACTG[A/C]AGCCCCAAACTCCTG	8925
rs543727452	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63784748	AAGTAACTGGGACTA[A/T]AGGTGGCTGCCACCG	8925
rs543739955	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63666810	TAGTCATTTGTGACA[C/T]ATGCAGAGGGACTAA	8925
rs543745570	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63820757	TCCTGTGCTCAAGCA[A/G]TTCTCCGGCCTTGGC	8925
rs543752980	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63738460	AATTATATAATGGTT[A/T]TGTAAGACATTAACA	8925
rs543772774	snp	C/G	4.97566e-05	0.00498757	intron-variant	HERC1	GRCh38.p7	15:63733165	AGAACAATAAAATAG[C/G]AACAAGTAACTAGCG	8925
rs543773079	snp	G/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63741028	TACATCTATGTTGTT[G/T]TTTTTTTTATTTTTT	8925
rs543777826	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63615649	AAATAAATTCATACA[C/T]ACATACAGAGGAATT	8925
rs543779296	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63637898	GATGAAAGAAAAAGG[A/G]AGGGGTGATGGGGAA	8925
rs543802449	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63654817	GAGGTTGCGGTGAGC[C/T]GAGACTGCGCCACTG	8925
rs543823736	snp	A/G	4.77794e-05	0.00488748	synonymous-codon	HERC1	GRCh38.p7	15:63655815	TAGCAATGCCACAAG[A/G]GCCTGTGTTACAACA	8925
rs543823737	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63662889	AAAAGACTTTTTAGA[C/G]TGTTTCAACTCTAGG	8925
rs543830434	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63615271	AAGGCACTGGGTATG[C/G]AGAAAAAGGCCTGAG	8925
rs543834045	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63617622	TAGTTTACAGTCCCA[C/G]CAACAGTGTAAAAGT	8925
rs543838850	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63805029	CTTGGCAGTTTATCA[C/T]AAACACACGCTGTAC	8925
rs543868068	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63821338	GGCGGGCGGATCACG[A/C]GGTCAGGAGATGGAG	8925
rs543880970	snp	A/G	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63760023	GGTCTATCACAGCCA[A/G]TGTGGTGGCTCATGC	8925
rs543882204	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63615264	CCGATTTAAGGCACT[C/G]GGTATGGAGAAAAAG	8925
rs543888338	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63715667	ACTGAATGCACACTT[G/T]AACTGGAAATAGCCA	8925
rs543891453	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63621735	CTCGCTTCATTTCAT[G/T]CATTTGATCTTCCAT	8925
rs543903991	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63814716	TCAAGTTATCTGCCC[A/G]CCTCGGCCTCCCAAA	8925
rs543915528	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63719568	TATTTTTGAAAGCTC[A/G]CTCTGCTGAGTGGAG	8925
rs543929470	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63672444	TGAGGACAACTGTGC[C/T]TTCAGAAACACAGGC	8925
rs543975136	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63770667	TTAAGAATCACACAA[A/G]TAAATACAATTTACC	8925
rs543976460	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63631496	GCTCATCAGTGACCT[C/G]TCTTCCCACTCCTTT	8925
rs543977113	snp	A/G	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63763597	TTTTTTTTTTTAATG[A/G]GCAAGACTATAGTGT	8925
rs543984389	in-del	-/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63769934	CATACTAAATGACAA[-/T]TTTTTTTCCCCTCAC	8925
rs543995207	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63793306	TGGTTGCAGTAAAGA[A/G]GCTGGCCCAAACCCA	8925
rs544016010	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63803472	TGATGCCCAGGCTGG[A/C]GTGGCAGCGACACAA	8925
rs544016686	in-del	-/TCT	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63617005	TTTCTAAAATCATTA[-/TCT]TTTTTTTTTTTTATT	8925
rs544022215	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63684954	GCGGAGGTTGCAGTG[A/C]GCCAAGATCGCACCA	8925
rs544033763	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63800690	TTATATATAATTTGT[A/G]CGATTTGTTTAATGT	8925
rs544047080	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63646763	CAGTGAGCTGAGATC[A/G]TGCCACTGTACTCCA	8925
rs544095187	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834938	GGCGTAGGAGAAGCA[C/T]ACAAACATACAAGCC	8925
rs544131920	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63751750	ATATATATTTGATTT[C/T]ATATAACTTAAGGTA	8925
rs544168222	snp	C/G	0	0	intron-variant	HERC1	GRCh38.p7	15:63633267	ACTATAAATGGTGGT[C/G]AATCTGAATATAAGC	8925
rs544174214	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63656412	ATGGATTTCTTAAGG[A/G]ACCATTTGCAGTCCC	8925
rs544208395	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63665848	TAGAAGCATTTATGA[C/T]GGGATATATAATAAA	8925
rs544224331	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63625393	CTGGTAGAAGTGGCT[A/G]GCAGACTTTGTAGAA	8925
rs544226522	snp	C/G			upstream-variant-2KB	HERC1	GRCh38.p7	15:63835005	ACAGACGAGGGAGTG[C/G]TTTCCCATGGTTAAA	8925
rs544239383	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63809710	TCAGTCAACATTTTC[G/T]TAGTGTAGTTTTAAT	8925
rs544245952	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63665389	ATACAAAAAATGAGC[C/T]GGGCATGGTGGCACA	8925
rs544246854	snp	A/G	6.63196e-05	0.00575807	missense	HERC1	GRCh38.p7	15:63775173	CATCAGTGCTTGACC[A/G]GGGGCGTTCACTAAC	8925
rs544258722	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63783720	CTATTGGTAGACCAT[A/G]AATTCCTTTGAGAAT	8925
rs544277250	snp	C/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63673909	TTTGTATTTTTAGTA[C/G]AGACAGGGTTTCACC	8925
rs544279896	snp	C/T	0.000128733	0.00802185	intron-variant	HERC1	GRCh38.p7	15:63723372	TAAAAAAAATACTCA[C/T]GTTACCAATTTTAAC	8925
rs544296051	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63807052	CACCCGGCCTGAGTG[A/G]TTTTTTTAAGGCTCA	8925
rs544325248	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63815992	CATGAGGGTAACCAT[A/C]CCCACGATTCATTTA	8925
rs544334138	snp	C/T	0.488786	0.0740357	intron-variant	HERC1	GRCh38.p7	15:63739195	ACAACCACTAATATA[C/T]TTTTTTTTTTTTTTT	8925
rs544341318	in-del	-/TAAGGAGGAG	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63615164	GAGGACAAACAGGAC[-/TAAGGAGGAG]TAAGGAGGAGTAAGG	8925
rs544365229	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63766486	CTAGATACTTGAGAG[A/G]CTGAGGCAGGAAAAT	8925
rs544367984	in-del	-/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63708494	CTAAATCAAATCCTG[-/C]CAGAAACGAGGGAGC	8925
rs544373459	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63795798	CAGTTTCCACTGGCT[A/G]GAACGGGACCTGACA	8925
rs544376308	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834453	TCATCGCAGCGGCCC[C/T]GGCCCTCCGGCCGGC	8925
rs544396211	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63772168	TAAACTATCCAGTCA[A/G]TTATCAAATATGCAT	8925
rs544406064	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63782369	AAGAATTATTATAAA[A/C]CTACTCTCCCTGTGC	8925
rs544419111	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63762837	AAAAGCTGAGTGTTG[C/T]GAGGGAAACTGAGGC	8925
rs544423747	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63730198	GGTAGCTCACACCTA[C/T]AGTCCCAACACTTTG	8925
rs544437711	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63702879	GGGAGACCAAGGTGG[A/G]GGGATCACGAGGTCA	8925
rs544458508	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63788665	CTCATGCCTGCAATC[A/C]CAGCACTTTGGGAGG	8925
rs544461466	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63666797	TCATGTACTTTTGTA[G/T]TCATTTGTGACATAT	8925
rs544509050	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63802100	GTGCAGGAGGAAGAG[C/G]CCATTTGCAAAGTTC	8925
rs544511145	snp	C/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63765983	TTTACACTCATCTCC[C/G]AGGCATTGTCCTTAA	8925
rs544527295	snp	A/G	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63803273	TCCAGGAAGGGAAGT[A/G]GAGGTACAGAGAGGC	8925
rs544532130	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63795040	CACTGCATTCCAGCC[A/C]GGGCAACAGAGCAAG	8925
rs544547211	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63768171	ACTGTTTCTCTTATT[A/G]CTGGGTCATCTGCTA	8925
rs544551924	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63670937	CCAGGTGCGGTGGCT[C/T]ACATCTGTAATCTCT	8925
rs544556526	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63732231	GTCTCAAACTCCTGA[C/G]CTCAGGTGATCCACC	8925
rs544560237	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63782892	GGAAGTAACTGCAGA[C/T]GTGGTGGAAATAGCA	8925
rs544573637	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63637192	TTTAATGAAATACAT[C/G]CATGATTGCTACTGC	8925
rs544580099	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63809579	AGACCAATCCTGGGC[C/T]ACTGCAAAAGTTGAG	8925
rs544599129	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63775910	AGGCATGGTGGCACA[C/T]ACCTCTAGTCCCAGC	8925
rs544605706	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63822159	GAGTCTGCCTGGCCC[A/G]GTCAGGGAATACGGA	8925
rs544606144	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63770992	TTAGGAGTTCGAGAC[A/C]AGCCTGGCCAACATG	8925
rs544641886	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63735550	AAAGTATAAAAAAAA[A/T]AAAAAGAATTACAGA	8925
rs544642819	snp	A/C	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63822546	AGCCGAGATCATGCC[A/C]CTGCACTCCAGCCTG	8925
rs544645844	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63786443	TGTTCATATGAAAAC[C/T]TGTACACAAACATTC	8925
rs544647388	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63797657	AATAACTCTGTCTCA[G/T]GCATGGCATGGCCAG	8925
rs544648916	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63682105	TTAAATATTGCTGGG[G/T]AAAAAGAAAGAGACG	8925
rs544674437	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63831720	CTTGGAACGTTGGAA[C/T]TGTTATTACTATTTA	8925
rs544676488	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63685364	TGCTGCCTATTATAT[A/G]TTCTGATTACAGGTG	8925
rs544687692	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63688229	ACATTTTAAAGACGA[A/G]CCAACAGAATCTAGA	8925
rs544708115	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63789380	CAGGCGTGAGCCACC[A/G]CGCCCGGCCAAAAGG	8925
rs544724589	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63687453	TGAGACAGAAGAATC[A/G]CTTGAACCGGGGAGG	8925
rs544725808	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63647313	GATATCATCTCACCC[A/C]AGTCAGGATGGTTAT	8925
rs544735222	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63643221	TTTTCTAGGACACAG[C/G]TGATTTTAAAAACAC	8925
rs544757328	snp	A/C/G	0.0111801	0.0739322	synonymous-codon	HERC1	GRCh38.p7	15:63747017	GGTAGCTACCCCTCC[A/C/G]GCAAGTGCAAGAGCA	8925
rs544789908	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63774501	CTTCTGATGCAGTAG[A/T]CTTAACACTGTACCA	8925
rs544816767	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63765441	GATTCAGGCCAGGAC[A/G]GGAAGTGGGAGATCG	8925
rs544819366	snp	C/T	0.0637235	0.166737	intron-variant	HERC1	GRCh38.p7	15:63619853	ATATCCCCTTTGTCA[C/T]TTTTTATTGCGTCTA	8925
rs544827772	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63810080	AGGAAGATCTACAAT[G/T]ATTTGGAATGTATTA	8925
rs544829059	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63670990	GCAGATCCCCTGAGG[C/T]TGGGAGTTCGAGACC	8925
rs544866745	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63710501	CACGTGCTATTATAG[A/G]TGCTTGGGATACAGA	8925
rs544882802	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63627123	GAAATTGTCAGTGCG[C/T]AGGCAGCTCTGCTCA	8925
rs544883206	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63702328	TTTCACCCATACATG[A/T]TATACCATGAAACAC	8925
rs544908606	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63637991	GACTAGCTGAGGTAA[A/G]GAAGAGCAAAAGAGA	8925
rs544909186	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63622711	TGAAGGGGATAATAG[A/G]TGTAAAGCACTTAAA	8925
rs544923879	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63813259	ATCCATTTTACAACA[A/C]AACAGGTTCTTTTCC	8925
rs544939174	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63771709	AAGTGCTGGGATTAC[A/G]GGTGTAAGCCACCAC	8925
rs544954751	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63727563	CTTAGGATAGATAGA[C/T]TCCAATGGAAAAACA	8925
rs544969213	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63771772	CTCTGCCCCAATAAG[C/G]AGCTATATTATAGGG	8925
rs544970636	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63630093	ATATCAACTGATGTT[C/T]CCAGGACCTAATCTC	8925
rs545001484	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63728483	TATCTAATGAGGAAA[G/T]GTTTCAGTTTCACAG	8925
rs545021867	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63684924	TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG	8925
rs545056238	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63825480	TATATCAAAACATCA[A/T]GTGTACACATTAAAT	8925
rs545058971	in-del	-/TTGTTTTGTT	0.00676609	0.0577691	intron-variant	HERC1	GRCh38.p7	15:63681176	CTGAGACTAGGTGTA[-/TTGTTTTGTT]TTGTTTTGTTTTGTT	8925
rs545061761	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63738289	AATTGTTGCAGGACA[C/T]TAAATTGTTACAGAA	8925
rs545074008	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63807416	AGGGCTACAGGTCCT[C/G]ACCACTAGCTTGGCT	8925
rs545075178	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63799821	CAGGTTTCAGGAGCC[A/G]TTCCTAAATCAGACT	8925
rs545080899	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63776844	AGTGAAAGTGCACTT[C/G]AGATTTTTACATTTC	8925
rs545103064	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63741094	AGTGCAATGGTGCGG[C/T]CTCCACTCACTGCAA	8925
rs545111854	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63800510	TTAAACAGTACAGTA[C/T]CAGAGATATTAATTA	8925
rs545115131	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63785690	GGGATGATCCCTTGC[A/G]CTCAGGAGGTCAAGG	8925
rs545128651	snp	A/G	1.65688e-05	0.00287821	missense	HERC1	GRCh38.p7	15:63698846	CCACTCACAAAGCTT[A/G]CAACATTTTCAATCA	8925
rs545134506	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63691110	CCTCTCTCCGTCCAT[G/T]CACTGACTGTCTCAC	8925
rs545149750	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63707482	TCTGGTGGGGGGATG[C/T]AGACAACTGCCTACT	8925
rs545160820	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63820947	CTTAAACACTTGCAA[A/C]CAGAACAAGAGCTAA	8925
rs545177639	snp	A/G	3.56646e-05	0.00422268	intron-variant	HERC1	GRCh38.p7	15:63713305	TCAGTGCATAAAGTA[A/G]TAAAGGGAAGTGAGT	8925
rs545187729	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63696747	TATATGTGAAGGTTT[A/C]AAAACTATAAGGTAG	8925
rs545203384	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63757455	TAATTTTAGTAGAGA[C/T]GGGGTTTCACCATGT	8925
rs545230195	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63686793	AAAATTACATAATAG[A/G]TATAGTAGAAACATA	8925
rs545231344	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63730265	TTCAAGACCAGCATG[A/G]GCAACACAGCAAGAC	8925
rs545235372	snp	C/T	0.0111196	0.0737302	intron-variant	HERC1	GRCh38.p7	15:63780638	GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAGGC	8925
rs545261893	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63826902	TGAGAATGCAAATTG[A/G]TATACTTGTGGAGGA	8925
rs545263056	snp	G/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63693782	CAGACTCTAAGCAGA[G/T]ATGTTTGGTCAGAAG	8925
rs545295249	snp	A/C	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63629528	AATTCTAATCTCCAA[A/C]CCTCTATACTTAGGG	8925
rs545295963	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63823629	CTCAATTCTCACAAG[G/T]ATGGTACATAACTAG	8925
rs545296368	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63819191	TTCTAGGCTTTGGTT[A/G]CAGAACCAGAACCAG	8925
rs545301954	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63794288	CGCCCTGAATTCTTT[C/T]TTGCGTGAGATCCAA	8925
rs545349147	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63796717	GAAAGGCTGGACAAC[C/T]TGAAGCAGAAGCTTT	8925
rs545357943	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63687926	AGAACTACAAGAAGA[A/C]GGCAAGTTGCTTAGA	8925
rs545362623	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63626472	TTCACAAAAATAAAG[C/T]CAAATTTTTCCTTTC	8925
rs545363064	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63771164	ATTGCACTCCAGCCT[A/G]GGTGGCAGAGCAAAA	8925
rs545372035	snp	C/T	0.00953873	0.0683987	intron-variant	HERC1	GRCh38.p7	15:63739002	TTTTTTTCAAATTGA[C/T]ATATAATCCACATGC	8925
rs545395595	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63725856	ATTCTGAGTTTATTC[C/T]TCCAAAATCAACACA	8925
rs545397220	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63682457	TCCTCCAGTGGGAGG[G/T]GAAAGGGTTCAAAAA	8925
rs545402177	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63787688	GAGGATCACTTGAGG[C/T]CAGGATTTCAAGGCT	8925
rs545426471	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63653392	GGACTACAGTGAGCC[A/G]AGATCTCACCACTGT	8925
rs545465399	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63699561	TGGGTTTCATTAATA[C/T]AAGGAACATTCTCAC	8925
rs545470601	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63748943	CCTCCTTGATTTAAA[A/G]TATGACAATTTTTTT	8925
rs545470919	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63802341	CTTAGAAAAGGAAAA[G/T]ATTTGCTGAGTTTGC	8925
rs545489895	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63653335	GTAATCCCAGCTATG[C/T]GGGAGGCTGAGGCAG	8925
rs545502166	snp	C/G/T	0.00159617	0.0282053	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835440	AACAACAAGCAAAAG[C/G/T]TCCTCCTTTTAACTT	8925
rs545510615	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63803221	TTAAATTTAAAAAAC[C/T]AATAAAAAGAAAAAA	8925
rs545526292	snp	C/T	0.00636936	0.0560724	intron-variant	HERC1	GRCh38.p7	15:63790349	TTTAGGAGGCCGAGG[C/T]GGGCGGATCACGAGG	8925
rs545527365	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63696458	TCATATGAATCTATT[A/C]TAAGATAAACATTTA	8925
rs545528202	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63657040	TATTTCTGTTGGATA[C/T]ATACCCAGAAGTGGA	8925
rs545535721	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63714512	TGCACAAATTTGGAG[C/T]GAAGACAGTATTCTT	8925
rs545540094	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63616278	TGTTTAAACTGCTGC[A/G]GTTGAGCTGCTAAGG	8925
rs545576527	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63639409	CCGTATAGTCTTGTT[C/G]CAAGTAGGCTGTATC	8925
rs545617993	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63679177	CATCATTCGAACCAG[A/C]ACATGACAGAAACTA	8925
rs545623794	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63773553	TTATTTTTTTTTATT[C/T]TATTTTATTTTTGAG	8925
rs545629203	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63823322	GAGTCAACTGGCATA[C/T]AGATAGTATTTAAAG	8925
rs545634681	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63826153	ATGTGTTCCAAGCAC[C/T]TGGAGCAGCACTCTT	8925
rs545645424	in-del	-/A	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63810014	AATAATAAACTGGTT[-/A]AATAAATTATACACA	8925
rs545649481	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63634201	TTCAAATGTCTGTGG[C/T]TAAACCATAATCAGT	8925
rs545657927	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63697617	CCACCACCACGCCCA[C/G]TTAATTTTTGTATTT	8925
rs545664240	in-del	-/A	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63781853	ACATAAATGATAAAG[-/A]AGTGAAATCGCCTTT	8925
rs545682003	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63732292	AGGCATAAGACACCG[C/T]GCCTGGCCTGAAGGG	8925
rs545702636	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63792293	AATAAAATAATCTCC[A/G]AAGTCCTTTCCACTT	8925
rs545706738	snp	C/G			upstream-variant-2KB	HERC1	GRCh38.p7	15:63835864	CTATTTCAAGAAAAG[C/G]ACTGCTTACTTTAAA	8925
rs545710215	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63780109	TGCATTAGATTTATG[C/T]ACTTTCAGAAAATAG	8925
rs545715744	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63737405	CGTTTTTCCAGATAT[A/G]TATATATATATCTTT	8925
rs545722170	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63736755	GGGATTACAGGCATG[C/T]GCCACCATGCCCAGG	8925
rs545735499	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63707620	CAAAAAGCTTGTGTC[A/G]AAGAAGGCCCGGAAG	8925
rs545772092	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63790434	TACAAAAAATTAGCC[A/G]GGGGTAGTGGCGGGC	8925
rs545791361	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63746028	TGTTCTTTATTTTTT[A/T]AATTTCACTCTAATC	8925
rs545803531	snp	A/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63753227	TTCTGATAGCTGAGG[A/T]TGTTAACAAACGAGC	8925
rs545817122	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63739724	TGCGCCTGCAGTCCC[A/G]GCTACTCGGGAGGCG	8925
rs545822806	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63703535	AGTAAATGCAAATGC[C/T]GTATGAGGGAAAACA	8925
rs545827929	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63621060	GCTGGTTATTTTGCT[C/T]GTTAGTTGATGCAGT	8925
rs545828983	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63609874	AATGATAATTATGAT[G/T]ACTGGCAGCAAAACA	8925
rs545853616	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63762994	AGCTGTAGACCATGC[A/G]CCTGCCCTTTTGACC	8925
rs545864378	snp	C/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63613442	AGACTCACCACTGTT[C/G]AAGGTTTGTTTCATA	8925
rs545876480	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63619770	CTTCTAGATTTTCTA[A/G]TTTATTTGCATAGAG	8925
rs545885288	snp	C/T	4.64846e-05	0.0048208	synonymous-codon	HERC1	GRCh38.p7	15:63718619	AATAAGTTCAAGGTT[C/T]TTGCAAGCAAGTAAA	8925
rs545900644	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63676254	CTGAAACAAGGCAAA[C/G]AATGAGAGGAAAGGT	8925
rs545920266	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63726016	AGACAGAGTCTCGTT[C/T]TGTCACTCAGGCTGG	8925
rs545927798	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63717632	GCCGAGGTGGGTGGA[C/T]CACTTGAGGTGTTCA	8925
rs545932889	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63762282	ATAATTCAATGTGCT[C/G]AAACTCAAATAGGCT	8925
rs545934009	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63619113	TTTTTGCCCATTCAG[C/T]ATGATATTGGCTGTG	8925
rs545961442	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63741218	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	8925
rs545978300	in-del	-/CTAAGT	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63649667	GCAAATGCCAAAAAG[-/CTAAGT]CTAGAAAGGAAGTTG	8925
rs545998511	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63747227	CACTTTGGGAGGCGG[A/T]GGTGGGTGGATCACC	8925
rs546029760	snp	A/T	0.000106264	0.00728841	synonymous-codon	HERC1	GRCh38.p7	15:63634802	AGAGGTATTTCCAAG[A/T]CCCAGACGACCATAG	8925
rs546033560	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63791757	GCAGTCCCTCTCTCA[A/G]TGTGAAAATTTAGAA	8925
rs546045467	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63615241	TCCAACCAAAGACCA[A/T]TTCAGAACCGATTTA	8925
rs546065201	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63612698	GACCGCCAGGCACGA[C/G]AGTCAGTCAAAAAGG	8925
rs546108537	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63621646	CAGATGTAGATTTGG[C/T]CTTTTCACATAGTCC	8925
rs546110104	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63790918	CCTATCCTATTATTC[C/T]TTTAATTTGGGTATA	8925
rs546113202	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63648442	TTTCATTCTTTTTCA[C/G]GTGGTTGTTGAAAAA	8925
rs546128498	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63643181	GCTAAATTCAGCAAC[G/T]TCCAATCACATACCT	8925
rs546183135	in-del	-/ATTTTAC	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63615977	ATGACAGCAAAAAGT[-/ATTTTAC]ATACAAATACGGCAC	8925
rs546192010	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63763433	GATAAAGAAACATAA[A/G]GAACTGCATCATGAG	8925
rs546195244	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63646777	CGTGCCACTGTACTC[C/T]AGGCTGGGTGACAGA	8925
rs546195824	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63752377	GTCTATAATTATACC[C/T]GGCTCCTCCCTATCC	8925
rs546196805	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63769771	TGAGGCAGGAGAATC[A/G]CTTGAACCCGGGAGG	8925
rs546202713	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63661183	TAATAAAAACTGCTG[C/G]TATGTAGGTACACAC	8925
rs546204937	snp	C/T	0.000399281	0.0141238	intron-variant, missense	HERC1	GRCh38.p7	15:63669408	CATAGCTCAGTTTAA[C/T]GGGGCAGTTCCCCTT	8925
rs546206276	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63827433	TGTCTTAAAAAAAAA[A/G]AAGACCGAAGAAAAT	8925
rs546208993	snp	A/G/T			intron-variant	HERC1	GRCh38.p7	15:63818393	CTACTCTGAAATAAG[A/G/T]AGCCAAACCGACAGA	8925
rs546226117	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63810850	ATAAAGAAGGAAAAT[A/G]GCACTGAGTGCCTCC	8925
rs546229927	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63707177	CCTAAAGCCTTGAAG[G/T]AGTGCCTTATTTTCC	8925
rs546258314	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63657247	TATCTCATTGGTGGG[C/T]TTTTTGTCTTAGGTT	8925
rs546273115	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63627972	TTGACTGCTGTGCCA[A/G]TGCACAGACATCATG	8925
rs546328718	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63756930	TTTTCATGCTCACAA[C/T]TTTGTTGCTGAGTTC	8925
rs546347060	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63649151	CAAGGTGAGGAGATC[A/G]AGACCATCCTGGCCA	8925
rs546357074	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63748490	AATATATATTTCATA[C/T]TAAGAAAAATATCCT	8925
rs546361962	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63777093	GGTAATAGAGAGAAA[A/C]CTCAATCACTGAAGG	8925
rs546366711	snp	C/T	0.00161275	0.0283509	missense	HERC1	GRCh38.p7	15:63713578	GGTGGATCATCAGCT[C/T]GAGCCCCAGACCCTG	8925
rs546394617	snp	A/C/T	9.93591e-05	0.00704767	missense	HERC1	GRCh38.p7	15:63645038	TCTGCACTAGTCACA[A/C/T]TGGTCTGTGTAGTAT	8925
rs546397177	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63643847	AGACAGGAAAATACT[A/G]ACTACTTTTTAACCA	8925
rs546399405	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63730336	TGGTGGTGCACACCT[C/G]TAGTCCCAGCTACTT	8925
rs546400882	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63780526	GGAGATTGAGACCAT[C/T]CTGGCTAACACGGTG	8925
rs546426400	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	HERC1, FBXL22	GRCh38.p7	15:63608691	ATTAAAACAAAATAA[A/G]TATATGAATATTCAT	8925
rs546428586	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63755472	GGAGGCTGTGTTCAG[A/G]CCAAGGATGACTGGC	8925
rs546457639	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63679738	TTCTATTATTCAGCT[A/G]ATAGCATCTTATTAC	8925
rs546462188	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63698335	AGGCAGGAGAATCAC[C/T]TGAACCCAGGAGGCA	8925
rs546462548	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63777806	ATAGGTAATCACCTA[C/T]ACAAAACCACCTTGA	8925
rs546491505	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63743338	ACAATCTGGGCTCAC[G/T]GAAACCTCCACCTCC	8925
rs546505217	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63804415	ACATGGTGAAACCCG[C/T]CTCTACTAAAAATAC	8925
rs546539460	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63750200	TTATCATATAAAATG[A/G]ATTATATAAATCACA	8925
rs546553936	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63773798	ATCCACCCTCCTGAG[A/C]TTCCCAAAAGTGCTG	8925
rs546566346	snp	A/G	3.31241e-05	0.00406952	missense	HERC1	GRCh38.p7	15:63661810	TACTTCTCCCTGCAG[A/G]TGCCACATAACAGGT	8925
rs546586644	snp	C/T	2.77412e-05	0.00372422	synonymous-codon	HERC1	GRCh38.p7	15:63672543	CTCGGATGCAGGCAC[C/T]GTTTCTGTGTCAGTG	8925
rs546593806	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63793938	GCACAAAATACAGGT[C/G]ATAAAGACCTTCTAA	8925
rs546597556	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63609836	CAGTCCATCCATTCA[A/G]CTGACGGTGATGCAT	8925
rs546609761	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63706929	AAATTCATGTAATTA[C/T]AGCAATGTCTTACTT	8925
rs546627168	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63672201	AAAAAATACTCAAAA[A/T]CTTAGGGGAAAAAAT	8925
rs546664710	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63806483	TACTCTGCCTGGTTT[C/G]TTATTATTTGCGTAC	8925
rs546677426	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63820941	AAATAGCTTAAACAC[C/T]TGCAACCAGAACAAG	8925
rs546678897	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63671159	GGTGAGCCCAGATCG[C/T]ACCACTGCACTCCAG	8925
rs546689468	in-del	-/T	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63734388	TCTTTATACAAACGA[-/T]TTCAGACAAAGTTCT	8925
rs546691224	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63805529	GGAACTTTCTGGGTA[G/T]GATGAAAAGAGACTA	8925
rs546704701	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63712978	AATTGGAGCACAGAG[A/G]TAATATACACACACA	8925
rs546719174	snp	C/T	0.00597247	0.0543191	intron-variant	HERC1	GRCh38.p7	15:63780676	ACGGTGAGCCAAGAT[C/T]GTGCCACTGCACTCC	8925
rs546727801	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63806011	TGTCCACCCAATGCT[A/G]GTATTCCCAAAAGTT	8925
rs546737578	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63763227	ACTAATAAAAAGAAA[C/T]GATAGAATTAGAATA	8925
rs546759378	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63631048	CAGTGGTGCGACCTC[A/G]GCTCACTGCAGCCTC	8925
rs546789776	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63686263	ACATTTACATATCAC[A/G]ATTTTTTTTCAGTCT	8925
rs546800900	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63832836	AAGGATAAAAAAAAA[C/T]GTGTCTGTTAGGAAA	8925
rs546814312	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63697523	GCAATGGCGCGATCT[C/T]GGCTCACTGCAACCT	8925
rs546824072	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63742660	TATTCCTAGTTTGTT[A/G]AATATTTTTATCATG	8925
rs546824382	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63639036	GTGTTTTCTGAACAC[C/G]CACAGGTACAAGGTC	8925
rs546852733	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63793551	AATAATTCACCCCTT[G/T]TTTAGTATATAATCA	8925
rs546856307	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63693317	GGTGTGATCTCAGCT[C/T]ACTGCAATCTCCACC	8925
rs546862115	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63807385	TCCCTTCCCACCTCA[C/G]AAAGCCATTTCCTCT	8925
rs546863379	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63652321	AAATTTCAAAAAATT[G/T]TAGTGACAATATGAT	8925
rs546887305	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63707634	CAAAGAAGGCCCGGA[A/T]GTGACAAAACAAGGC	8925
rs546890631	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63801217	AATAGGATATTTCCC[A/G]TGTTCTGTGAGCCAT	8925
rs546891447	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63786923	CAATAAATTATTATT[A/T]TTTTTTTTTTTATTT	8925
rs546895057	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63692827	TAATAAAGAATTATT[A/G]GTGACTAGAGAACAG	8925
rs546898414	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63658876	CTTAGGAGAAACTCA[A/C]ATATTTCTAAGTTTG	8925
rs546945454	snp	C/T	1.65679e-05	0.00287814	missense	HERC1	GRCh38.p7	15:63638755	TTTGTTCATCCATGC[C/T]GTTAATCCATTTACT	8925
rs546962675	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63832158	TGTCATGTGATTTGG[C/G]GGAAATATTATGACT	8925
rs546980774	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63723028	ACTATTTTCCACAAA[A/G]GGAAAAACAAATTGT	8925
rs546987322	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63623965	ATGATATCTTCCCAT[C/T]AGTGAATGAAAAAGC	8925
rs547009527	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63680458	ATAATCTATAAACTG[A/G]ATACGTGGCACTTGA	8925
rs547010129	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63695479	CAACCTCCACCTCCC[A/G]GGTTCAAGCGATTCT	8925
rs547012569	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63611847	AGCATGAATCGGCAG[A/G]CCTACTTGAGGGTCA	8925
rs547018057	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63730686	AAGAAAATGTCCTGG[A/T]TTTTTAAAAATACAT	8925
rs547026030	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63761345	AGTACTTTGGGAGCC[C/T]GAGGTAGAAGGATCA	8925
rs547031423	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63820434	ACGATGCTTCTAAAT[G/T]TTATTAACATTGAAA	8925
rs547039137	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63768584	TCGTTATCTAAAAGC[C/T]AACTCTAGTGATCAC	8925
rs547044000	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63687118	GACATTAGGGAGACC[C/T]ACACAGAATGATGTA	8925
rs547049508	snp	A/G	0.00993419	0.0697739	intron-variant	HERC1	GRCh38.p7	15:63610273	AATGCACCAGAGCCA[A/G]TGATGACACAGCTCA	8925
rs547049707	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63635424	CAGCCTCAGGAAGCC[C/G]AAGCTGAACAGCATA	8925
rs547067903	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63668269	TTAAAAAAAGCAAGA[C/T]TCCCTTGAGGTCAGG	8925
rs547073165	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63668634	AAAGCAGGAGTGGCT[A/G]TAACATCAGAGAAAG	8925
rs547073626	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63783339	AGCCATTAACATCAA[C/G]GCAAGACCCTCCATG	8925
rs547073874	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63713341	ATGTTTTCAGTGTCT[A/C]GTCAGTCCCACCTGG	8925
rs547112268	snp	A/C	0.000798881	0.01997	intron-variant	HERC1	GRCh38.p7	15:63776341	TGTCCCTCCTGTAGA[A/C]TTCTTTCTCTCAATA	8925
rs547127456	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63709207	TTTGGCATGTTCCCA[C/G]GCTGGTCTTGAACTG	8925
rs547133512	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63822805	AGGCAGAGATGACAA[A/C]ATGTGATCAGATTAG	8925
rs547142952	snp	G/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63704974	CGATCTCCTGACCTC[G/T]TGATCCGCCCACCTC	8925
rs547147985	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63760290	CTTAAATCCCAACTC[A/T]TTCTAAGAGTTCAGG	8925
rs547156212	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63659339	TCACCATAACCTCAA[A/G]CTCCTGGGATTAAAC	8925
rs547156701	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63729920	ATCCCAGCTACCGGG[C/G]AGGCTGAGGCAGGAG	8925
rs547209870	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63671845	CTAACCATTCTGCTT[C/G]CCTTATTTCACTTAA	8925
rs547234946	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63804459	GGCATGGTGGCGGGC[A/G]CCTGTCATTCCAGCT	8925
rs547243543	in-del	-/A	0.0154538	0.0865337	intron-variant	HERC1	GRCh38.p7	15:63613676	ATTTATTATATATAT[-/A]AAAAAAAACTGGGCC	8925
rs547264312	snp	A/C/G	4.9689e-05	0.00498418	missense	HERC1	GRCh38.p7	15:63716355	TCATCCTCTGGCTCC[A/C/G]GATGCCCCTCTTCCC	8925
rs547279735	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63813702	TACCATTGTATGCCT[A/G]TGTTTCTGTATGTAC	8925
rs547281847	snp	A/G	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63807828	TCCTCTGTAATGCCC[A/G]CCCCTTCCTTTCCAC	8925
rs547298586	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63804012	TGATGCTTATCTAAA[A/G]TGTCAAGGCAGTTTA	8925
rs547307197	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63617685	GTTGTTTCCTGACTT[C/T]TTAATGATCGCCATT	8925
rs547312024	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63767010	GGTTTTTCATTTGTT[C/T]TTTTTTTTTGAAATG	8925
rs547318009	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63798053	ACTTGTCAAAACACA[C/T]ATGTCCAAGTCCCCA	8925
rs547327244	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63624826	TATAATTACCATTTT[A/T]AAAAACCTTAGAAAA	8925
rs547363235	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63823521	AGCTGGGGGAAAGAA[C/G]AGATCTAACTGGTGA	8925
rs547382216	in-del	-/C	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63740122	CACCATTTGGCCAGG[-/C]TGGTCTCAAACTCCT	8925
rs547386015	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63726226	ACCTCAGGTGATCCG[A/G]CGGCCTCAGCCTCCC	8925
rs547390185	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63627489	GACCAGCCTGGCCAA[C/T]ATGGCGAAACACCAT	8925
rs547391464	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63649379	AACAAAACACACACA[A/C]AAAAAACAATTTCAT	8925
rs547401951	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63816989	AGGGAAAAAAAAATA[C/T]AAACCAACCTATCAA	8925
rs547411683	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63824391	ACAAAAAAATTAGCC[A/G]GGTGTGGTGGCAGGC	8925
rs547421215	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63725572	TTAAGATTCAAAATA[C/T]TTCTCATAGTCTCCT	8925
rs547429772	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63792747	CAATCTTGCAGCAGA[C/T]GCTAGCTGGGTGTCT	8925
rs547454267	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63808645	AGTAAAGTAAGTTAT[C/T]CACTTGTCAAGTTCA	8925
rs547454518	snp	C/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63634418	CTCAAGGATACCAGA[C/T]AGGAGCTACTAGTAT	8925
rs547477613	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63830014	TCCAATTAATAAATG[C/T]AGAAGGAATGAGGGA	8925
rs547481376	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63689265	TTTCGTACTTTGATA[A/C]AAGATAAATGGTGGG	8925
rs547481632	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63655216	AAAATTAGCCGGGCA[C/T]GGTGGCATGTGCCTG	8925
rs547499286	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63697949	TTAAAACCACAATAA[C/T]TAATAAATATTTGGG	8925
rs547501182	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63705372	GTTGCCCAGACTAGC[C/T]TTCCGAAGTGCTGGG	8925
rs547544753	in-del	-/AT	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63622666	AAGAGGATAACAACA[-/AT]ATTTACTCCTTAGGG	8925
rs547547919	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63720413	GTTCATTTGACAGAT[C/T]TGCTAAATATCTGGG	8925
rs547557483	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63732519	GAGATTTAGAATTAA[C/T]GGCATACTAATACAG	8925
rs547562350	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63743624	AGGCATTCTTCAAAA[C/T]GTCAATTGCATTTAT	8925
rs547567432	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63769612	TAATCTCAGCACTTT[C/T]GGAGACTAAGGCAGG	8925
rs547586983	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63821326	TTAGGAGGCTGAGGC[A/G]GGCGGATCACGAGGT	8925
rs547605662	snp	A/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63614870	GCAAGTTGAGGAAAC[A/T]AGACCTAAATTCTGG	8925
rs547616661	snp	C/T	2.3248e-05	0.00340932	intron-variant	HERC1	GRCh38.p7	15:63655994	GACTTAATTTTTACA[C/T]GTAATTTTGGAACAA	8925
rs547617997	in-del	-/T	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63791892	CAGTAACATCTCCTA[-/T]TATTGATGCCCCACA	8925
rs547619244	in-del	-/CTT			intron-variant	HERC1	GRCh38.p7	15:63657454	CTCTTTTGTGAAACA[-/CTT]CTTAATGTGTTTTGT	8925
rs547619265	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63627862	TTTGTGTAGCTATAC[-/A]AAAAATTTCATAATA	8925
rs547643439	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63741488	CGGCTAATTTTTTGT[C/T]ATTTAGTAGATACGG	8925
rs547650210	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63621777	TTTCTTCCAGTTGAT[C/T]GAATCGGTTACTGAG	8925
rs547666446	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63769368	GGAGCTGCAGTGAGA[C/T]GAGATCTTGCCACTG	8925
rs547713403	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63621306	TTCTTTTCTTTAAGA[A/C]TGTTGAATATTGGCC	8925
rs547718868	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63794871	AGGAGTTCAAGTCCA[C/T]CCTAGCCAAAATGGC	8925
rs547722114	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63727235	GAGGCAAGATTGCGC[C/T]ACTGCATTCCAGCCT	8925
rs547725328	snp	G/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63628178	GGCGGATCACTGGAG[G/T]TCAGGAATTTGAGAC	8925
rs547725613	snp	A/C	0.0588605	0.161139	intron-variant	HERC1	GRCh38.p7	15:63620649	TCTTTGTAGGTCACT[A/C]AGGACTTGGTTTATC	8925
rs547738784	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63819189	ATTTCTAGGCTTTGG[C/T]TGCAGAACCAGAACC	8925
rs547754327	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63631514	TTCCCACTCCTTTCA[A/G]AGCCAGCTCTCCCAA	8925
rs547783051	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63615680	AACACAGTAAATACA[C/T]ATTAGCAGATTTTGG	8925
rs547785201	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63741290	CCTCAGCCTCTCAAA[A/G]TGCTGGGATTACAGG	8925
rs547788211	snp	C/T	3.31559e-05	0.00407147	missense	HERC1	GRCh38.p7	15:63638452	CTGCTGCAGGTACCA[C/T]TACATTTCTTCCAGC	8925
rs547806790	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834524	TCCACCTTGTTCATG[C/T]CTTTGCGCCTTATGG	8925
rs547815942	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63649233	TGGCGAGTGCCTGTA[A/G]TCCCAGCTACTTGGG	8925
rs547849755	snp	A/C	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63798484	CCAAGCCTTCAAACC[A/C]CTGCTTCTATCCTCT	8925
rs547867247	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63701646	TCTGCTGAGCCCTAA[C/T]GGATGAAATTAACCC	8925
rs547882176	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63793076	GCAGGATATGGGGCA[A/C]GGGGCCCAGGGCTTT	8925
rs547905866	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63700862	AATATCATAGATGCA[C/T]AATGTATTAAGTTAA	8925
rs547911176	snp	A/G	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63619208	TTTTTAGCATGAAGC[A/G]TTGTTGAATTTTGTC	8925
rs547968846	snp	A/C	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63818778	ACTGCCACATATCTG[A/C]CTTTTTAGAAGCTAC	8925
rs547972192	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63764334	AAATCCTAACATTAG[A/G]TCATGAAACTAACTT	8925
rs547975621	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63779485	AACATAAATAGAAAC[A/G]CTAATAACGTGAGAC	8925
rs547987195	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63731402	CCCAAAAGCAGTTAG[C/T]ATTTTATTTCCATTT	8925
rs547988113	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63794576	AAATTCATTAGCACA[C/T]AAAAAGACACAGATC	8925
rs548005144	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63811917	CTATTGTTAACCATG[G/T]TCTTCCTGATGGAGC	8925
rs548007929	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63670617	CCTGGTGAATGCCTA[C/T]GGGAGCAAGGGGGCA	8925
rs548008296	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63678487	TTCATACATGTGAAT[C/T]ATACCAACTGGCCCC	8925
rs548026787	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63751371	GTAGTAGGCTACACC[A/G]TCTAGGTTTGTGTGG	8925
rs548038513	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63827822	AAAAGGAATGAAGTA[C/T]TGATACATGCTACAA	8925
rs548041818	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63729862	ACCCTGGTCTCTACT[A/G]AAAAATACAAAAATT	8925
rs548078008	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63821887	TGCTTTCATGGAGTT[C/T]ACATTCTAGTAAGGA	8925
rs548081714	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63684567	TTAAAAAATTTAAAG[C/T]TGTAATTACTAAATG	8925
rs548082565	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63676766	GTCTCAAAAAAATAA[A/G]TAATAAAATCAAATA	8925
rs548101574	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63759810	TAGCACATGAAATGG[A/G]AGAGGATAGGGTCAT	8925
rs548101756	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63726943	ATGACACCTTACTCA[A/C]CTGATAGACTGAATC	8925
rs548101974	in-del	-/T	0.000488911	0.0156274	intron-variant	HERC1	GRCh38.p7	15:63651227	AACTACTTTCAGCAG[-/T]TTACTAGTGTTTACA	8925
rs548113587	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63636762	TACTTTCACATAGCA[C/T]CTATGAAACAGATAC	8925
rs548148283	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63744996	GTACTGAGTCCTTTT[C/T]TTCAAGGCAGTGGGT	8925
rs548150786	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63761500	GCTGAGGCTGGAAGA[C/T]CACTTGAGCCCAGGA	8925
rs548177101	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63634599	AACAGTTAAAATTAT[C/G]AATTAGACCATAGCA	8925
rs548186663	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63752809	TCCTTCTCAGATACT[C/T]TACTTCAAACAGAAG	8925
rs548188066	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63827292	CCAGGTATAGCGGTG[C/T]ACACTTGTAGTCCCA	8925
rs548189538	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63687228	ACTAATCAGGATATC[C/T]CTGCAAGTTCAGGTA	8925
rs548212568	snp	C/T	0	0	intron-variant	HERC1	GRCh38.p7	15:63795245	AATTGTCTTAGTTAC[C/T]AAAGCTTGCCTTTTT	8925
rs548241629	snp	A/C			upstream-variant-2KB	HERC1	GRCh38.p7	15:63834433	CGCCCCACGCTCTTT[A/C]TCTCTCATCGCAGCG	8925
rs548269484	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63617638	CAACAGTGTAAAAGT[C/G]TTCCTATTTCTCCAC	8925
rs548275401	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63626657	GATTCATGAGGCTTT[C/T]ACTACAAGAATAAGA	8925
rs548277052	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63810593	TAACCTTTTTTATAC[C/T]ATGTAAGTTTCTTAA	8925
rs548287632	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63633425	TTCATGGACTCAGAT[A/T]TCCTTTGTATTGTTT	8925
rs548305555	snp	G/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63724674	TTATAGAATCAAAAT[G/T]AGAAGCCTAGAGAGA	8925
rs548344821	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63666296	TTAAAAGTTATGTTG[C/T]CTTTAATAAGCTAGG	8925
rs548353017	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63720416	CATTTGACAGATTTG[C/T]TAAATATCTGGGCTA	8925
rs548367205	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63613967	GAACAAGCTGTTATG[C/G]TTGGTGGAACACAAA	8925
rs548389920	in-del	-/CACC	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63776423	AATTGTAGAATGGAA[-/CACC]CACTTTGGAAAGGTG	8925
rs548390450	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63618635	TCTTCCTACCCATGA[C/G]CATGGAATGTTCTTC	8925
rs548393325	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63673538	AAAGTACCCAACACA[A/T]AGTAGGTACTCAACA	8925
rs548399847	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63822207	AGTGGAATAAACAAG[A/G]AGAGGGAGGCAGGGA	8925
rs548420895	snp	C/G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63716709	TTTTGATTAAAATAT[C/G/T]ATGCTGTAAATTTAT	8925
rs548428711	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63687472	GAACCGGGGAGGCAG[A/T]GGTTGCAGTAAGCAG	8925
rs548430156	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63681448	GCAATCCTCCCACCT[C/T]GGCCTCCCAAAGTGT	8925
rs548436300	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63814894	ATTCATATGAAAGTA[C/T]TTTAATGCAATGTAC	8925
rs548441734	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63665579	CATTAAATCAATGTC[C/T]AATATTAAAATGAAT	8925
rs548441924	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63636536	TCGGCCTCCCAAAGC[A/G]CTGGGTTTACAGGCA	8925
rs548453424	snp	A/G	4.0744e-05	0.00451335	intron-variant	HERC1	GRCh38.p7	15:63640480	TATAATATGTCAAAG[A/G]GTTTGTGCCAAATAT	8925
rs548460311	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63641386	CCTCAGACCTCATGC[C/T]TTTAAGGGATAAGTT	8925
rs548462268	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63664963	TACGTTATGAAAATA[A/T]TCACTGAGCTTGTTG	8925
rs548468795	snp	C/T	0.000614674	0.0175203	intron-variant	HERC1	GRCh38.p7	15:63680783	AATATAAAACTAAAA[C/T]AAAAGTGGGATATTC	8925
rs548475288	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63695361	AATTTTAAATGCTTG[A/G]TAATTGTTGAGTCTG	8925
rs548488302	snp	C/G	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63788869	AACAGAGCAAGACTC[C/G]GTCTCAAAAAAAAAA	8925
rs548491207	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63646854	AACAAAACAAAACAA[A/G]AAAAAGCAACTATCT	8925
rs548499916	snp	A/G	4.96849e-05	0.00498397	missense	HERC1	GRCh38.p7	15:63663072	AACATAGCTTCCATC[A/G]CCTCATCATCAAGAT	8925
rs548512726	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63739479	TGGGATTATAGGCGT[A/G]AGCCACTGCACCCAG	8925
rs548513934	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63653469	TACAATTCAATCTTC[A/G]TTTCTTGTTACAGCT	8925
rs548518186	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63753424	AATATACAGGTACTA[C/T]ATGCGTATAATTTTT	8925
rs548520120	in-del	-/T/TT/TTT			intron-variant	HERC1	GRCh38.p7	15:63622326	GAAGTGCCTGTTTCC[-/T/TT/TTT]TTTTTTTTTTTTTTT	8925
rs548539873	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63764261	AAAATTAGTTAAACA[A/G]TCTACAAAAACAACA	8925
rs548543127	snp	A/G	0	0	intron-variant	HERC1	GRCh38.p7	15:63660154	TGAAACCCCATCCCC[A/G]CCAAAAAATACAAAA	8925
rs548545307	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63648220	ATGATCAAAACAAAA[C/G]AGTAAGGAAAAGATA	8925
rs548549690	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63688719	TCACAAAAACCAAGA[C/T]AGGAATTAAGGTAAA	8925
rs548551899	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63745659	TGCCTATTCAGGACT[C/G]TTTTTTCTATCTCTT	8925
rs548556435	in-del	-/AT			intron-variant	HERC1	GRCh38.p7	15:63737400	ATATCGTTTTTCCAG[-/AT]ATATATATATATATA	8925
rs548575551	snp	A/C/T	5.64467e-05	0.00531226	missense	HERC1	GRCh38.p7	15:63696294	TACCTTTTTCTTCCA[A/C/T]CCCAGACAATAGAAC	8925
rs548577788	snp	A/G	3.74329e-05	0.00432609	synonymous-codon	HERC1	GRCh38.p7	15:63756689	ATAGCTGCCTTTCCC[A/G]CAAGCTCTAACAGAG	8925
rs548578178	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63666907	TTTCAGCTCTCATGT[A/G]AAAAACAAGTGTCCT	8925
rs548581273	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63796277	ATATTTTCCAACAGT[C/T]ACATCTTCTGCAACT	8925
rs548581913	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63662510	ACCAATGTATATACA[A/G]ATCCACCATGTACCT	8925
rs548592059	in-del	-/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63653608	TTGCAGATAGATTCC[-/T]TATAAAAATGGGGTA	8925
rs548598673	snp	A/G	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63619296	TATATGCTGGATTAT[A/G]TTTATTGATTTTCGT	8925
rs548646196	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63802756	AAAACTGAAATAAAC[A/G]AGTTACTGCAAGTAA	8925
rs548653803	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63717356	GTCTACAAATGGAGA[A/G]AAAGAGTTTGGTTTT	8925
rs548678538	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63663417	TCACTGGGTTATTGA[C/T]AGGTTTAAGTAAGAG	8925
rs548686050	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63718192	GTCCTTCTATGACAT[A/T]ATTTTTGGACTTTAT	8925
rs548691505	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63709335	TAAAAATGGGTTTTT[C/T]TTTAGTCTTTTTAAA	8925
rs548700469	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63767684	GCCTGGGAAACAAGA[A/G]CGAGGCTCCGTCTCA	8925
rs548708012	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63628915	AGACATAAATAAGTT[A/G]ATAACTGTACCATGC	8925
rs548723005	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63748844	AAATTCAATCTCCTA[A/G]TAGTGACTGAAACTC	8925
rs548740084	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63739940	TTTTCAGACAGAGTC[A/T]CACTCTGTTGCCCAG	8925
rs548768690	snp	A/G	0.000330216	0.0128452	missense	HERC1	GRCh38.p7	15:63649859	GACCAGGCTGTAGCC[A/G]GACCCTCTTCTGGCC	8925
rs548837100	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63771059	CCAGGCATGATAGCA[A/G]GTGCCTGTAAACCCA	8925
rs548881375	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63796848	ACCAAGGTTTTATCA[C/T]GCAGATGAGGCCTCC	8925
rs548887941	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63749176	CTTGCTTCGGAAACA[A/T]GTCTAACCTCAACAT	8925
rs548896502	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63831630	AGGTCAGCTCCTTCA[A/G]TATACCCAGCCCCCT	8925
rs548909646	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63757504	ACTCATGATCTCAAA[C/T]GATCCACCCGCCTTG	8925
rs548927565	in-del	-/TAT	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63644755	ATCAATTATATCCAC[-/TAT]TATCACAGTAACAGT	8925
rs548943708	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835254	GTAAAGCTCACATAC[A/G]GCACATATTAAGTAC	8925
rs548954590	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63679309	AAACAGTTCTCAGCT[A/G]GCCTTAAATTATAAT	8925
rs548959904	snp	A/T	1.69057e-05	0.00290733	intron-variant	HERC1	GRCh38.p7	15:63712766	TTTACTGAATCTGGG[A/T]ATACCTACCAGTGCG	8925
rs548962171	snp	A/T	0.00529097	0.0511614	intron-variant	HERC1	GRCh38.p7	15:63809518	ACACATCAGGAGCTG[A/T]GGATAACACTAAGAT	8925
rs548971959	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63652022	GCCTAGGCAGCAGAG[C/T]GAGACTCAGTCTCAA	8925
rs548991309	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63678719	ATCCTCAAGGCTCCA[A/G]AATGATGAGTCCTGG	8925
rs548992797	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63811800	GGCGACTCAGTGAGA[C/T]TCCGTCTCCAAAAAA	8925
rs548993296	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63686213	TGTATATCCTTCACT[G/T]GGTTTCCATTTATAT	8925
rs548993605	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63805360	TGAATCTCAAAAGCA[A/T]TATGCTAAGCGAAAT	8925
rs549000849	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63833345	CCACCCCGCTAAAGG[C/T]GGCCGGCGCCTGGGG	8925
rs549019204	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63776725	AATCCTAACATTCAG[A/G]GACGCCAAGGCAGGA	8925
rs549030169	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63685657	GTCAATATTACTGGC[C/T]AATCTTATCCCCCTG	8925
rs549039050	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63621847	CAGCTCCATCAGGTC[C/G]TTTAAGGACTTCTCT	8925
rs549048281	snp	G/T	0	0	intron-variant	HERC1	GRCh38.p7	15:63786806	GAATTATGAAAATGT[G/T]TTGGAACTAGAGACG	8925
rs549050095	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63707921	ATGACAGAGCAAGAC[G/T]CCCTCTCAAAAAAAA	8925
rs549052228	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63818501	AAAGACATCTTAAAT[A/G]CGAATATAAAAATAT	8925
rs549054174	snp	A/C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63811384	AGTTGCACCAAAATG[A/C/T]TGCAATTTGTGAATC	8925
rs549056002	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63677663	ACTAGTATTTCAAAG[A/C]ACATGGGTTTAGGAA	8925
rs549057454	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63770216	CTCCAGCTCCCCTGA[C/T]ACACACACCTCACAA	8925
rs549063542	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63780256	TTGATTTTGTGATTA[C/T]TATGAATGGAATTTC	8925
rs549091718	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63693623	CTTGTCAGGATCAAA[C/T]GCTAAGAAAACATCT	8925
rs549123419	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63737349	CAACAAAACACTTCC[A/G]GATATATATATATCT	8925
rs549125180	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63644398	AACATTGGATTCTTA[C/G]CATCTATAGAAAAAA	8925
rs549142916	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63820364	CATTATACATGACTG[A/T]ATACTTGGTTATATA	8925
rs549185317	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63765180	ATCTACTGAGCGCCA[A/G]AGAAATACATAATTC	8925
rs549196128	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63638306	TTTAATGATTCCTCA[C/T]AATAGATTATGAAAT	8925
rs549197343	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63710569	GCTTATATTCTAATG[C/T]AGACTAAGACTAACT	8925
rs549197464	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63807224	TACCCTTCAAGCTCT[A/G]CTTTGCACCCTGTGA	8925
rs549220517	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63692741	GGTCAGAAAACAAAG[A/C]CTAAACTTGAAACGC	8925
rs549229525	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63799352	CAAAAATTAAAAAAT[C/T]AGCCAGGCATGGTGG	8925
rs549229828	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63609808	CATAAGGAAGGGGCA[C/G]TCAATTAAACTCCAG	8925
rs549236332	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63813601	AAATAATTTTTTACC[G/T]ACTCACCTAGCCTTT	8925
rs549245985	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63699121	ACTCATGTTTGAATA[C/T]GCGCATGCATTAAGT	8925
rs549258403	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63773197	CCTGTAATCCCAGCA[C/G]TGTGGGAGGCCAAGG	8925
rs549273155	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63806633	GGGCTCAGAACATTG[C/T]AGAAGAGGAATTAAT	8925
rs549291083	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63609438	AGGCCCTACTGCCCC[A/G]TGGCCCTCGAGGCTC	8925
rs549322142	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63706371	TGTGTACACGTGTAC[A/G]GGGTAAGAAGTTCTC	8925
rs549324730	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63664794	TGAGCAATAACTTTG[C/T]CTGATTTTGAATTCT	8925
rs549325448	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63721594	ATTGGCAGATCTGAA[G/T]AATATGTATCTCATT	8925
rs549333670	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63638999	ACTATCACTATGGCA[C/T]TGGTGATTCAAAGCT	8925
rs549347316	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63617327	CATTCATGTCCCTAC[A/G]TGACATGAACTCATC	8925
rs549359352	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63682997	AAAAATTAGCCAGGC[A/G]TGCTGATGCGTGCCT	8925
rs549361990	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63672007	CCTATTAAAATAGAG[G/T]TGGCTAAAGAAGCAT	8925
rs549364822	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63729898	GGCGTGGTGGTGGGT[A/G]CCTGTAATCCCAGCT	8925
rs549373010	snp	C/G/T	4.97082e-05	0.00498518	missense	HERC1	GRCh38.p7	15:63630507	CATACACATCTCCAT[C/G/T]TGATGCCAAAGCAAG	8925
rs549410778	snp	C/G/T	0.000101463	0.00712197	intron-variant	HERC1	GRCh38.p7	15:63758151	AGATTATCTACCAGT[C/G/T]TGTAAGCTATTTAGA	8925
rs549415484	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63825795	TTGAGATGGAGTCTC[A/G]TTCTTGTCCCCCAGG	8925
rs549452699	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63789814	TCAAAATAAATAAAT[A/T]AATAAATAAATAAAT	8925
rs549462046	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63644883	ATTTCCCAATGGATC[C/T]TGCCCTTTGGGATAT	8925
rs549476547	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63779744	ATTCAGGCCAGGCAC[A/G]GTGGCTCACGCCTGT	8925
rs549487456	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63790502	AGAATGGCATGAACC[A/C]GGGAGGCGGAGCTTG	8925
rs549490102	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63822352	GCACTTTGGGAAGCC[A/G]AGGCGGGCAGATCAC	8925
rs549504410	snp	A/C	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63674337	AAAAAAATCAGATAA[A/C]ATACCTTGCTTAATT	8925
rs549562763	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63750496	TCAGCAATCTGAATG[A/T]TTTTTTTTCTTTATC	8925
rs549585157	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63800762	TCCTTTGTGATAGGG[A/G]AATAGGAGCATCTTT	8925
rs549595623	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63830524	ATTAGACCCTAGAAC[-/A]AAAAAAAAAGGCATT	8925
rs549600764	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63647629	GGATGACTGGATAAC[A/G]AAAACATGGTATATA	8925
rs549604271	in-del	-/AAAC	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63652061	AAACAAAACAAAACA[-/AAAC]AAAAAAACTGTTGAA	8925
rs549606985	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63759669	TTGACTTGTATGAAC[A/T]CAATACAATAAAGAT	8925
rs549651718	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63828574	AAACTCCCAACCTCA[A/G]GTGATCCGCCCTCCT	8925
rs549663375	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63717993	TGATTGTTACCCTTT[C/T]GTCCTAGTTGTGTCC	8925
rs549709477	snp	A/C	0	0	intron-variant	HERC1	GRCh38.p7	15:63630967	TGACACAGTTCAGGC[A/C]CTCAAGTTTCTTATG	8925
rs549711670	snp	C/T	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63783306	ACCTTTCAGCAACCC[C/T]CATCCCGATCAGTCA	8925
rs549743828	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63803547	CCCACCTCTGCCTCC[C/T]AAAGTGCTAGGATTA	8925
rs549773404	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63732353	TTTAATATAAAGAAG[G/T]TATTTAATACAAAGT	8925
rs549777453	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63641912	GTCAATAATTAACTA[C/T]TTCTTCAGAACCTGC	8925
rs549794402	snp	A/G	0.00119737	0.0244387	downstream-variant-500B, missense	HERC1, FBXL22	GRCh38.p7	15:63608273	CTTCCTCCTTGTCTG[A/G]TAGAGTCGCCCTCCA	8925
rs549810645	snp	A/T	0.0146672	0.084371	intron-variant	HERC1	GRCh38.p7	15:63739915	CACTTAGCATATTTT[A/T]TTTTTTTTTTTTTCA	8925
rs549811816	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63661661	TCAGGGAAGGTTAAA[C/T]GTAACTCCTCACGTG	8925
rs549814269	snp	G/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63641274	CTTTATTTTACTCTG[G/T]TGAAAATAAAGCAAG	8925
rs549826820	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63742754	TTTTTTCTATTAATA[C/T]GGTGTATTATATTGA	8925
rs549849982	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63614747	ATATTTATGACCACA[G/T]GAGTGGTCACTCATT	8925
rs549858437	in-del	-/TT	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63631574	GATGAAGTTTCGCTC[-/TT]GTCGCCCAGGCTGGA	8925
rs549867489	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63632108	TTCAACATAACTAAA[A/T]CTAAATTCCTTACCC	8925
rs549886640	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63711467	GCACAGAGATATTAA[C/T]GCAGATGAAGGAGAA	8925
rs549889043	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63747329	GCTGGGCATGATGGC[A/G]GGTGCCTGTAATCCC	8925
rs549927615	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63781695	AAAGGAAGACACCAT[A/G]TCCCTCACTTTAAAT	8925
rs549939427	snp	C/T	0.0023933	0.0345097	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835732	AGTAGAGATGGGGTT[C/T]CACCATATTGGCCAG	8925
rs549947175	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63739354	AAGCACACGCCACAA[C/T]GCCAGGCTAATTTTT	8925
rs549947884	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63734395	ACAAACGATTTCAGA[C/T]AAAGTTCTCAGCATG	8925
rs549971808	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63762577	TAATCCACCCACCTC[G/T]GCCTCCCAAAGTGCT	8925
rs549978218	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63660853	TAAGGGAAAATTTAA[A/G]TTAACATGTACACAA	8925
rs550003106	snp	C/G	3.34303e-05	0.00408828	missense	HERC1	GRCh38.p7	15:63675068	GCAATGGTTCACAGG[C/G]TTCCAGATTATACAA	8925
rs550004060	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63635748	ACGAAAAAGACCATT[C/T]TAACCAATACTAACA	8925
rs550007689	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63621185	CTCTTTTAGGGCAGG[C/G]CTGGTGGTGACAAAA	8925
rs550008261	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63763068	TACCGTGGGGTCCCA[A/G]AGCTCAGGGCCTTTG	8925
rs550009451	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63798595	AGAACTTGAAAACTA[A/G]TGCTTTCTAATTCTC	8925
rs550027386	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63627402	ATAGGCTGGACACAG[C/T]GGCTCACACCTGTAA	8925
rs550035097	in-del	-/AA	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63757056	AGAATGGCAAGACAT[-/AA]AGTTTTCCTTCCTAT	8925
rs550074254	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63714588	GGAGTCTCACTCTGT[C/T]GCCCGGGCTGGAGTG	8925
rs550082542	snp	A/G	1.65669e-05	0.00287805	missense	HERC1	GRCh38.p7	15:63725381	TCTGGAGACACAGGG[A/G]AGCCCTGAAGCATGC	8925
rs550102747	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63733304	ACCCAATTAATCCCA[A/T]TTAGGAAATGGGATT	8925
rs550106572	snp	A/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63741270	CTGACCTCGTGATCC[A/T]CCCGCCTCAGCCTCT	8925
rs550113289	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63648895	GCACTATGACTTTGA[A/T]TTACCCCACTTCCCC	8925
rs550113545	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63795430	GAAGTAGAGATAAAA[C/T]TGAGAGGAAAAAATA	8925
rs550120427	snp	C/G	1.83011e-05	0.00302493	synonymous-codon	HERC1	GRCh38.p7	15:63643452	TCCACCAGACACCAG[C/G]GCCAACCCATCAGAA	8925
rs550143655	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63743513	TGTGATCCACCCACC[C/T]TGGCCTCCAAAAGTG	8925
rs550152069	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63654936	TCAGTAGACTAAGAA[A/G]GCAGCAGAAATAATT	8925
rs550165232	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63824478	GGCAGAGGTTGCAGT[A/G]AGCTGAGATCATGCC	8925
rs550166723	snp	C/T	0.000399281	0.0141238	missense	HERC1	GRCh38.p7	15:63746998	CCTGCCTCCCGAGAA[C/T]GCTGGTAGCTACCCC	8925
rs550170294	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63611194	AGGCAAGCAGCCCAT[C/T]ATGACCAGAACATGA	8925
rs550188417	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63610614	GAAAATTTATGGAAA[A/G]GCTCTTTTATAATCC	8925
rs550195418	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63697846	GCCTATTTGTTAGAA[A/G]CAAGCCACTAAGTCC	8925
rs550201710	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63655141	GGAGGATCACACGAG[A/G]CCAGGAGTTCAAGAC	8925
rs550213836	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63803940	GTACTTTCATCAAGA[C/T]AGATCAACAGAACAG	8925
rs550216584	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63698399	CTACAGCCTGGGCAA[C/T]GAGAGCGAAACTCCG	8925
rs550228431	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63821893	CATGGAGTTTACATT[A/C]TAGTAAGGAAGACAA	8925
rs550244638	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63791138	TTGCAGTTTGGGGAT[A/G]AATACCTGAGAGATG	8925
rs550249970	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63609975	ACAATTGAGGCAAAG[A/T]CTATGAGGAATTTCA	8925
rs550256694	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63797844	CCGTAAGATAGTTAT[G/T]AATAACATAAAACAA	8925
rs550274031	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63785264	CATTACCTTGACAAA[A/G]TGTTTAAAAATTATC	8925
rs550290521	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63765092	TTGTTCCGAAGCAGA[C/T]AGCTACAGATGAAAG	8925
rs550294239	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63754840	TAAACTGGGTCATAG[A/G]GTCACTTCGGTGAAC	8925
rs550327108	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63824350	CATCCTGGCTAACAC[A/G]GTGAAACCCCATCTC	8925
rs550333647	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63639585	CATATTGTATCAATG[C/T]TTATCCAAATGTTTG	8925
rs550338358	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63661227	CAATGATTATTTTAC[A/C]AAACTACTGGGGAGA	8925
rs550349017	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63700696	CCTGGGTGACAGGGC[A/G]AGACCCTGCCTCAAA	8925
rs550369220	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63806578	CTGCCCTACTCTTTT[C/G]TCCCTTTCAGCCACT	8925
rs550370332	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63737748	ATTTTGAAATGTGAG[A/G]ACACAAAGGACAAGA	8925
rs550391187	snp	A/G	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63676741	AGCCTGGGCGACAGA[A/G]CGAGATTCCGTCTCA	8925
rs550408372	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63757514	TCAAACGATCCACCC[A/G]CCTTGGCCTCCCAAA	8925
rs550444953	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63758511	AAATAAAGATAACTA[C/G]ACTATTTACTCATAT	8925
rs550460621	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63683902	GACCTGACTATAAGC[G/T]AAAACCTGACACTGT	8925
rs550478151	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63784567	GCTCTTCACTGCATA[A/C]ATTTGAATTTCTTAT	8925
rs550494292	snp	A/G	0.000399281	0.0141238	synonymous-codon	HERC1	GRCh38.p7	15:63680620	GAGTAAAGCTGGACA[A/G]TGTGAGAGTCTGTTC	8925
rs550498642	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63690300	TAGTAAGAAATTCCA[C/G]ATTTTTCTTTCCTTC	8925
rs550507860	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63737079	AGTGTAAGACAGAAC[A/G]GGAGGCTACTAAAAA	8925
rs550561737	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63672372	GCTTGACTATATAAT[C/T]TCTTAGTTTCTTTCT	8925
rs550586937	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63831645	ATATACCCAGCCCCC[C/T]TTTTTTTCTATTTCA	8925
rs550599603	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63801065	TCAGGTTGGTGAACA[C/T]ATCAAGATGCTGGGA	8925
rs550614814	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63733335	TAGGAAAATGCAACT[C/T]ACAGGTTTTTATTTC	8925
rs550619712	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63657831	GGTTGGGACCAAGGC[C/T]TTTTTTTTCTATGTG	8925
rs550623088	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63787894	TGAGTCCAGAAGGTC[A/G]AGGCTGCAGTGAGCC	8925
rs550640528	snp	A/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63632115	TAACTAAAACTAAAT[A/T]CCTTACCCTTCCCCA	8925
rs550644575	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63794008	AAAACTGCGATGGCC[A/G]TGAGAGTGACCTCTG	8925
rs550649446	snp	C/T	0.000120361	0.00775667	missense	HERC1	GRCh38.p7	15:63645540	CGGCACCAAGCAATG[C/T]CATTTACAATAGATG	8925
rs550651860	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63786898	ATTGTACGTGATGTG[A/T]ACTTCAACTCAATAA	8925
rs550652753	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63664758	AACAGTTCAATTATG[C/T]ATATAACATTTCCTG	8925
rs550654035	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63623614	ATATGAGGCTCACAA[A/G]TGCATCCTTGCTACA	8925
rs550657276	snp	A/G	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63773895	GGTTTTCACAAAGGT[A/G]TATTTCAGTCTTACA	8925
rs550658597	in-del	-/AAG	0.00993419	0.0697739	intron-variant	HERC1	GRCh38.p7	15:63726467	TTAATAAAATTACTC[-/AAG]AAAAAAAGATGGCAC	8925
rs550663944	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63617755	TGCATTTCTCTGATG[A/G]CCAGTGATGATGAGC	8925
rs550670343	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63707205	TCCAAAATTACTACT[C/T]CTTCCTCTAGCTTCA	8925
rs550701130	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63631731	TGTTTAGTAGAGACG[A/G]CGTTTCGCCATGTTG	8925
rs550703870	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63760365	TCAAATCCCATATGA[A/G]GTTATTATAAAGTTG	8925
rs550705389	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63800744	TACTTGGTGTTCGTA[A/C]TTTCCTTTGTGATAG	8925
rs550726305	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63808118	CATTATAGTAATTCT[A/T]GTTGACAAAAAAAAA	8925
rs550752582	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63672752	TTTTTCAAAAATAAC[A/G]GCGGGAATAAAAAAC	8925
rs550769874	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63619973	TTGATTTTTTGAAGG[G/T]TTTTTGTGTCTCTAT	8925
rs550773371	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63624973	ACATAACATTTTTCA[C/T]AGTTAATATCATTCT	8925
rs550785791	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63660111	ATCACATGAGGTCAG[A/G]AATTTGAGACCAGCC	8925
rs550825195	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63687144	ATGTATATAGGAGAT[C/T]TCTGATCACATCTGT	8925
rs550836146	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63787571	AACAAATACTCAAAA[A/C]AAGTTCGCTACATCA	8925
rs550893749	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63665829	TATCAACTTTACATA[C/G]AATTAGAAGCATTTA	8925
rs550901078	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63693393	GCACTACAGGCATGC[A/G]TCACCATGCCAGGCT	8925
rs550916330	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63652928	ATTCTGGGATTACAG[C/G]CATAAGCCACCACAC	8925
rs550919679	snp	A/C/G	0.000295102	0.012144	intron-variant	HERC1	GRCh38.p7	15:63625929	TGGCGAGCATGTCAC[A/C/G]GGCACTGCTTACCAA	8925
rs550927965	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63753815	TATAAATTGTGCCAC[A/C]ATCAAATAAAAGAAC	8925
rs550930908	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63770083	CCAAAGCCTATAGCA[A/T]GGGATACAGGGCCCT	8925
rs550938932	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63695491	CCCGGGTTCAAGCGA[A/T]TCTCCCTGCCTCAGC	8925
rs550950061	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63716538	TTTTAAAACTTTAAA[A/G]AACCTTTAATTTTTT	8925
rs550955693	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63669763	TACATACATCACAAT[C/T]TTCTTATAGAAGAAT	8925
rs550960251	snp	A/G	0.00597247	0.0543191	intron-variant	HERC1	GRCh38.p7	15:63698406	CTGGGCAACGAGAGC[A/G]AAACTCCGTCTCCAA	8925
rs550972198	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63720834	TAACACTCTTTGTTG[G/T]GTTTTAAATTTAGCA	8925
rs550975356	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63702607	TTAAGTTTTATCAAA[A/G]TACCAAATTACTAAC	8925
rs550997032	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63717399	ACTAAATAATGGAGT[A/G]CAAAGCATCTGATTA	8925
rs551024672	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63638633	CTGTATGGGAGACAC[C/G]AGGGCACAAACACAC	8925
rs551034593	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63752144	TGTAATGATGAATAG[C/G]TTGAAGATTTTTAGA	8925
rs551043227	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63636566	ATGAGCCACAGTAAC[C/T]GGCCTAATTTCTTTA	8925
rs551044289	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63781445	TTATTATAACTGTTA[C/T]GGTAACCTGTAATCA	8925
rs551045961	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63821828	GTTTACCACATGCTA[A/G]GGACTTTTCTAGGCA	8925
rs551049917	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63814493	GAGATACAGTCTGGC[G/T]CTGCTGCCCATGCTG	8925
rs551056169	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63695228	TTTCTGTAGAGACAG[C/G]GTTTCGCCATATTGT	8925
rs551057274	snp	C/G	1.70866e-05	0.00292284	intron-variant	HERC1	GRCh38.p7	15:63628864	TTAGAAAGAGGAAGA[C/G]AGGAAGTCAATATGA	8925
rs551086567	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63777744	TTGGTCAAAAGAGTA[C/T]CCCTGCCCGACTCTC	8925
rs551091268	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63731331	CATTATTTTAAAATC[G/T]TAGAACAAATTTGGT	8925
rs551094913	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63715965	CCGCTCAGACGTCTT[C/T]GAGGCTGGTGGACAA	8925
rs551134330	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63752764	ACTAAGATTTATCTG[C/G]GTCACATATGCCAGG	8925
rs551136585	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63745623	ACCATACTGCCACTG[C/T]TGCAGGGGGAGGAGT	8925
rs551180860	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63663355	AAATTATACCTATCA[C/T]GTGTGTTTCCTCTCT	8925
rs551183929	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63785166	GTGGTGGCTCACTCC[C/T]ATAATCCCAACATTT	8925
rs551184198	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63727105	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	8925
rs551195713	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63697142	GTATTAATTAAAAGA[C/G]TATTTGGATTTTAGT	8925
rs551197915	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835238	GAGGAGTAAAATATA[C/T]GTAAAGCTCACATAC	8925
rs551243065	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63706337	GGGAAAAAAAATAGA[A/G]ACTTTTTATTTCAAC	8925
rs551262006	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63618572	GATGGGGATGGCATT[C/G]AATCTATAAATTACC	8925
rs551269797	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63656579	CATATACTTGAAGTA[C/T]AATTGAACTGACAAA	8925
rs551346174	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63772653	TGAGAGGATTTGAAT[A/G]TTGAATAAGAAAACA	8925
rs551355117	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63719705	GGCTGGAGAGTCCAC[A/G]TGCATTTTGAAGGCA	8925
rs551359907	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63627565	TGTAATCCCAGCTAC[A/G]TGGGAGGCTGAGGCA	8925
rs551361398	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63621437	TAACATTTTTTCCTT[C/T]ATTTCAACTTTGGTG	8925
rs551375205	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63825754	GAAAACCACGAAAAA[A/G]AAGAAAAATAATAAT	8925
rs551375532	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63708235	ATGGAAGAAAACAAT[C/T]TCAGGCCTCAGAACC	8925
rs551388882	in-del	-/TGTT	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63807807	TGCCCCCACTCATGC[-/TGTT]TGTTGTCCTCTGTAA	8925
rs551397163	snp	A/G	0.0298908	0.118541	intron-variant	HERC1	GRCh38.p7	15:63737623	GGCCTCAGGTGGTCC[A/G]CCCGCCTCGGCCTCC	8925
rs551403933	snp	C/G	0.00012219	0.00781536	intron-variant	HERC1	GRCh38.p7	15:63692584	ACAGTGAAGAGACAA[C/G]TTTACGTTACAACCA	8925
rs551407556	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63685161	GCAGTTTCCACAAAA[C/T]ACCTCGAGATGTCAT	8925
rs551409351	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63735059	ATAGCTAATCATCAC[C/G]TAACAAATATTTAGT	8925
rs551425230	snp	A/G	6.54815e-05	0.00572158	intron-variant	HERC1	GRCh38.p7	15:63764223	GCGGGACACAGCGTA[A/G]GAAGGGGAGAGACAT	8925
rs551437753	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63628287	GTCCCAGCTACTTGG[A/G]AGGCTGAGGCAGCAG	8925
rs551439527	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63786760	GCTGGAGAGGAAGGG[A/T]AAATGGAGAAACTGG	8925
rs551442659	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63691725	AAAATACCATGTGCC[G/T]TAGAGGATTACATTA	8925
rs551465246	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63831894	ATCAGGGTGCCTGCA[C/T]TGGAAATGGAATACA	8925
rs551488813	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63804440	AAATACAAAAAATTA[A/G]CCGGGCATGGTGGCG	8925
rs551497038	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63635666	AGAACTGTGTGGCAG[A/C]AGTTAAACCACACAA	8925
rs551497609	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63719085	GTGAACAAAACTAAA[C/T]CCCTGATCTAACAGA	8925
rs551516725	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63713785	AGAGGGAAAAATTAT[A/T]TTTTAGACATTATAT	8925
rs551517917	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63710789	TGCAGGCAATAGCAT[A/T]CCAGTCCTAAGAAAC	8925
rs551520584	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63722134	GCCTCCCAAAGTGCT[A/G]AGATTACAGGCGTGA	8925
rs551525864	snp	A/C	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63822558	GCCACTGCACTCCAG[A/C]CTGGGCAACAGAGCA	8925
rs551527011	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63792785	CAATTCAGTTATGAC[A/G]CTACTTACCAGGAGA	8925
rs551540019	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63649284	CTTGAACCAGGGAGT[C/G]AGAGGTTGCAGTGAG	8925
rs551549941	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63820108	ACACAAGAAATACAT[A/G]CAATTTTATCTGCCA	8925
rs551556835	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63649170	CCATCCTGGCCAACA[C/T]GGTGAAACCCTGTCT	8925
rs551580659	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609026	AGTATATCAACATCA[A/T]ATCAGAAGTGAGCAT	8925
rs551588517	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63790299	AAAGTACTTTTTAGG[C/T]TAGGCGCGGTGGCTC	8925
rs551596476	snp	A/T	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63698452	AGGCTCTGATGACCT[A/T]TTGTCATCAACTAGT	8925
rs551615917	snp	A/C	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63804593	CTGTCTCAAAAAAAA[A/C]AACAACACTGTTAAG	8925
rs551624320	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63747472	CTTAAAAAAAAAAAA[A/T]TTTTGTCAAGTCATG	8925
rs551629379	snp	C/G	0.000104902	0.00724156	synonymous-codon	HERC1	GRCh38.p7	15:63649789	ATCAACAACTTCAAT[C/G]AGTCCCAGAGATCCA	8925
rs551636516	snp	A/G	3.57226e-05	0.00422611	missense	HERC1	GRCh38.p7	15:63615778	CTCACCTGTCTGTCC[A/G]TCTCATGAAGTCGAT	8925
rs551651962	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63622960	GAACAAACCAATTAC[A/G]AGATCATACTGAAAA	8925
rs551657482	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63721443	AGGCAGGAGAATCGT[C/T]TGAACTCGGAAGGCG	8925
rs551693346	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63712684	ATTTTTATATGTCTA[A/C]AACAAACATATTACT	8925
rs551696339	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63755609	CATGGCAAAACCCTG[C/T]TTCTTTTAAAAAATA	8925
rs551712041	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63813456	TTACTTATCTTTTAA[C/T]CTAGGATAGTGCGAA	8925
rs551720165	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63671388	TAAAAAAAAAAAAAA[C/G]TGAGAGAGAAAAAAA	8925
rs551720480	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63712305	GGAGAGGAGAGGACA[C/T]TGGAGACACACTAAC	8925
rs551721787	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63753244	GTTAACAAACGAGCA[C/T]TTTTATTACAAGAAA	8925
rs551762456	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63735244	ATAGGGAAAGTAAAA[A/G]GGTGCAGGAACTTGC	8925
rs551769827	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63644888	CCAATGGATCTTGCC[A/C]TTTGGGATATAGTAA	8925
rs551808336	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63644273	ATGAGCAAAAGGAAG[A/G]CAACAGAATGTACAA	8925
rs551810393	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63742491	TATTTCATTATCTTA[C/T]ATAATTGCCCCAGCT	8925
rs551867236	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63786176	TTAAAGTGGGAGGAC[A/T]GCTGGAGGCCAGGAG	8925
rs551887669	in-del	-/TGGAATGAT			intron-variant	HERC1	GRCh38.p7	15:63647870	CACGGGCCTAGAGTG[-/TGGAATGAT]TGGAATGATAGACAA	8925
rs551893850	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63831274	ACCACGTCCAGCAAA[C/T]TTTTGTATTTACCAT	8925
rs551918866	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63717481	GCATTTATAATTTTA[C/T]GATCATGTTATCAAG	8925
rs551921034	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63656007	CATGTAATTTTGGAA[A/C]AAAAATATTTCATTT	8925
rs551927293	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609389	CATGGTTAAGTCAAG[C/T]GGACACAGAGACTGG	8925
rs551932252	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63687802	ATTAGGGAAGGCCTC[A/T]CTGAAGATGTGATAA	8925
rs551940844	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63813012	AGTAAGGAACTAGAA[G/T]AGCTAAAAACACACA	8925
rs551945039	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63671972	AGAAATTTAAGTAAG[C/T]ATCACTTGGAATTTA	8925
rs551949357	in-del	-/T	0.442655	0.159323	intron-variant	HERC1	GRCh38.p7	15:63771437	AGAAAAGCAATCTAG[-/T]TTTTTTTTTTTTTGA	8925
rs551957043	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63757834	TCTGCCTCAGCCTCC[A/C]GAGTAGCTGGGACTA	8925
rs551959650	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63689565	TATGCTGTTAAGAAA[C/T]ACCTTTTAGGAAAAA	8925
rs551970414	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63765083	CCTTTCCTTTTGTTC[C/T]GAAGCAGATAGCTAC	8925
rs551977530	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63806152	TGATGAGCATTTCTG[A/C]AGAACACAAGTGGTT	8925
rs551998726	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63807758	CCTACCAATTCCTAC[A/G]TCACTCAGTTGAGAT	8925
rs552002878	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63664067	GTGAAGCCCTAACAA[C/T]CACAGAGCAGTACAT	8925
rs552059389	snp	C/T	1.65701e-05	0.00287833	missense	HERC1	GRCh38.p7	15:63677987	CATCAACTCCTCCTA[C/T]CACAGCCAGCACGGG	8925
rs552061863	in-del	-/TTCT	0.00119784	0.0244435	intron-variant	HERC1	GRCh38.p7	15:63776342	GTCCCTCCTGTAGAC[-/TTCT]TTCTCTCAATAAATG	8925
rs552094382	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63629752	GAGGCTAATATGAAT[A/G]ATGCTAGACCTTGAA	8925
rs552094512	in-del	-/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63725675	TTTCTCTTTACCAGA[-/C]TGATTTAAAATAATA	8925
rs552102158	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63676790	TCAAATAAAATTTAA[A/G]AAGATATTGTTCTAT	8925
rs552131992	snp	G/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63772209	ACAATGAGGCTAAAT[G/T]GACACTGAGAAAAGA	8925
rs552138908	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63746255	ATCTTAAGTATTAAA[C/T]TTATCTTGTAATTTC	8925
rs552144611	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63723793	TTTAATAGACTTAAG[C/T]AAAAATAATCAGTTA	8925
rs552170624	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63647398	TCTTAAACACTGTTG[A/G]TTTGAATGTAAATTA	8925
rs552172545	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63640561	TTACTGTTTAAGCTT[C/T]TTGCTAGGAAATAAT	8925
rs552186228	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63613637	TATATTATCGTGTTG[C/T]ACACCTTAAATATAC	8925
rs552208139	snp	A/T	1.65762e-05	0.00287886	missense	HERC1	GRCh38.p7	15:63754564	GACAGAGCAATAGTA[A/T]GTGAACTGCCACAAG	8925
rs552209522	snp	C/T	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63646982	ACAATGAGCCATGCA[C/T]GTTGGCTCACGCCTG	8925
rs552215512	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63745549	ACAGGATAGCATTGA[A/G]TTCAATGCCTCACAA	8925
rs552232459	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63632363	GCCCCAGTCCCTAGA[A/G]GGGATGAAGAATGAG	8925
rs552249485	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63620181	TGTGTCCCAGAGATT[C/G]TGGTATGTTGTGTCT	8925
rs552261692	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63619437	ATCAATGTTCATCAA[A/G]GATATTGGTCTAAAA	8925
rs552291680	in-del	-/TT	0.0444908	0.142359	intron-variant	HERC1	GRCh38.p7	15:63644499	ATGTAAGCTTCTTTG[-/TT]TTTTTTTTTTCTGTT	8925
rs552295433	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63652823	AACTGGATAATTTTT[G/T]TATTTTTAGTAGAGA	8925
rs552295682	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835840	GTGCCCAGCCTGGTT[C/T]TGCCCATTCTATTTC	8925
rs552319767	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63626823	TTTATTATTATTGTT[C/T]GTAGTAAAAACTAAC	8925
rs552322900	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63642821	CCTTCTGCTACTAAA[C/T]AGTTGCACTGTTTTG	8925
rs552324710	in-del	-/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63788208	CAGTACAAGTCAGAC[-/T]TGATGATTTGGGGAA	8925
rs552340826	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63752696	AAGGTTTAAGGGAAG[C/T]TAAATGCTAAAACAT	8925
rs552350183	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63745047	GTCTAGAAATGTCAT[C/T]TGAGAGCTGGCATCT	8925
rs552364398	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63776242	CATGGCTATCTAACA[A/G]TTTTGGTTATGGTTG	8925
rs552385394	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63816141	GATCACTAGTTCCTC[A/T]AGATGTTATAAGGAG	8925
rs552397961	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63627251	TGGGGAATCTTAGGA[C/T]CCCCCCTAAGAAATA	8925
rs552401075	snp	A/C	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63768427	GGTATGGAATCATAT[A/C]AGAAGCTAAGTGTTT	8925
rs552410751	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63658234	CACAGACGGTCAATA[C/T]ATTTTGACCTTTAGT	8925
rs552440160	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63782676	CATTTTGTAAGGCTA[C/T]AGCTGCCACAGATAG	8925
rs552454973	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63688486	ATTTAAAACTTGGGA[A/G]TCAAGTCTTAAATGA	8925
rs552470807	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63689188	TTTCCAGAGGTAAAG[A/T]AAGAAGTGGAAAAAA	8925
rs552476061	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63717712	CCCATGTCTACTAAA[A/G]ATACAAAAAATTAGC	8925
rs552499129	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63648282	AGACTTTGAAACAAA[C/T]AATGATAATGCAACC	8925
rs552499859	snp	C/T	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63703800	GTCCCTCCCAGCTAC[C/T]TGAGAGGCTCAGATG	8925
rs552502898	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63648851	AAACAAAACAAACCT[C/T]TTCTGTTAATGGAAT	8925
rs552513058	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63830586	TCTATAGTCAATAGA[A/G]TTACACCAATGCTAA	8925
rs552520467	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63753670	GTTGTTGAAGACTAT[C/G]GGGAAGTAAGCATTC	8925
rs552527739	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63748238	CTCAAAAAATATATA[C/T]ATACATATATACATT	8925
rs552530832	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63641164	ATATATGTGTGGGTC[A/G]GAAAAGGGAAGATAT	8925
rs552535008	in-del	-/CT	0.442113	0.159977	intron-variant	HERC1	GRCh38.p7	15:63637800	TATGCAGTCCCGTAA[-/CT]CCTTGATGACTATAA	8925
rs552538880	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63745626	ATACTGCCACTGCTG[C/T]AGGGGGAGGAGTGGC	8925
rs552561544	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63660781	GGTCTTTGAAACCAC[A/G]TTCTTTTCCTTTGAC	8925
rs552604146	in-del	-/ATTTGGGTTTCT	0.00119808	0.024446	intron-variant	HERC1	GRCh38.p7	15:63788171	TTAACAAACAAATGA[-/ATTTGGGTTTCT]ATTCTATAATCCAGT	8925
rs552614699	in-del	-/CTC	0.00795532	0.062565	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835440	AACAACAAGCAAAAG[-/CTC]CTCCTTTTAACTTGT	8925
rs552652110	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63803890	ATAAAACTAGTAACT[A/T]GTAATCAAGACGTGG	8925
rs552664559	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63667766	CTAAAAATATAAAAC[A/G]AAGTACAGTTGACTC	8925
rs552680396	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63742195	TCAGTGTACAAGTCT[C/T]ACACTTCTTTTGTTA	8925
rs552717866	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63830185	TATGAACAATAAAGG[A/G]AAGAATAGTAACTTT	8925
rs552747825	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63701596	AAAACCTGATAAAAA[C/T]AGATGCCAGGTCAGT	8925
rs552753553	snp	C/G	1.68843e-05	0.00290549	missense	HERC1	GRCh38.p7	15:63656339	ACTCAAGACCAGCAG[C/G]CAGGCTACAACTGGA	8925
rs552800808	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63615482	AGGCGTGGTGACACA[G/T]GCCTGTAGTCCCAGC	8925
rs552817340	snp	A/C/T			intron-variant	HERC1	GRCh38.p7	15:63705645	TATCATGAAAAAAAA[A/C/T]TTTTTCACAGGCTTT	8925
rs552819465	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63823750	CAGTTGAAAGAAAAA[A/G]AGAAACTATACTATA	8925
rs552819773	in-del	-/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63702590	CAACCATAGCAAATC[-/T]TTTAAGTTTTATCAA	8925
rs552847317	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63791104	AATGGGTTTGTCCTT[C/T]CCTCGGACATACAGA	8925
rs552847822	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63630056	TAAAATATAAAAATA[C/T]TATTGTTTCATTCTT	8925
rs552848022	in-del	-/ACGTAGAA	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63760318	AGGAAAACTAATCCT[-/ACGTAGAA]ATAAGCAACAGAAAA	8925
rs552851400	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63720211	TGGGCTCAAGCGATC[C/T]TCCTGCCTCAGCCTC	8925
rs552887101	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63689324	TGAAACATGCAGATT[A/G]CTCTTCTAAGAAGCT	8925
rs552915109	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63819758	TTTCTATCAGCCAAA[A/C]CTATGTCATTGAGGC	8925
rs552921794	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63697190	TCCTTTTCCAGGATT[G/T]AATCCTAGATACCAC	8925
rs552947673	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63665000	GCTTGCATGCCATCT[A/G]GGACACAAGCCTTGG	8925
rs552953255	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63656701	TACCTCAGAAACCTG[C/G]TTTGGGCTTTTCTCA	8925
rs552968436	snp	A/G	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63786292	AAAAAAAAAAAAAAA[A/G]AAGAAGAAGAAGAAG	8925
rs552969536	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63609531	AAGCTCTGACTGGCA[A/G]GATTGCTTGAGAGAA	8925
rs552971073	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63830991	AACTTCTCTGTAAAT[G/T]ATTTGACCAACTTTT	8925
rs552973830	in-del	-/ACAAGCTTTATCCC	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63638324	TAGATTATGAAATGG[-/ACAAGCTTTATCCC]ACAATAAGACAAGCA	8925
rs552982006	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63664314	ATTTAAATAAAATTA[C/T]GTAAATGCATAGAAA	8925
rs552986298	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63806724	AAATCAGATAATAGA[C/T]TGCATTCTGCCTTTG	8925
rs552999543	in-del	-/ATC	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63726898	AAATTATAGAAAAAT[-/ATC]AGTTATAAACATAGA	8925
rs553007663	snp	C/T	0.00676609	0.0577691	intron-variant	HERC1	GRCh38.p7	15:63831644	AATATACCCAGCCCC[C/T]TTTTTTTTCTATTTC	8925
rs553034935	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63792474	AACCCTATCAGCAAA[G/T]CAGAATGAACGTGTG	8925
rs553037448	snp	A/T	0.00877176	0.0656425	intron-variant	HERC1	GRCh38.p7	15:63772507	TTATTTTATTGTTTT[A/T]ATATATATATATTAA	8925
rs553041772	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63735519	GTGCACATTGTGCAC[A/G]TGTACCCTAAAATTT	8925
rs553049164	in-del	-/AAAG			intron-variant	HERC1	GRCh38.p7	15:63699269	ACGCTGCCACAAGAA[-/AAAG]AAAGGCAGAAGCTGT	8925
rs553054358	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63631237	TTACCTTGCCAAACT[C/T]CTAGAGGGTGCCAGC	8925
rs553056462	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63758044	ATGAAAAAAACTAAT[G/T]CAGTATATAGACCAG	8925
rs553057722	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63670956	TCTGTAATCTCTGCA[C/T]TTTGGGAGGCTAAGG	8925
rs553058483	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63707453	GAAGTATATTTCTGT[C/G]TGTTACCTGTGTATC	8925
rs553068978	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63798961	ACTCAAAGCAAAAAG[A/G]GCACAAATAATTTCT	8925
rs553088200	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63638629	CAGCCTGTATGGGAG[A/T]CACCAGGGCACAAAC	8925
rs553095363	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63714370	TAGTTTTAATATATG[A/G]GGCAAGATTGCCTCC	8925
rs553106664	snp	C/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63693728	CAAGGAGAGGCTGAA[C/G]CTACAGAATGGGCAG	8925
rs553111285	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63711252	ATTGCTTGAGCTCAG[A/G]AGTTCGAGGCTGCAC	8925
rs553145433	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63812453	TTGAATACATCTATT[A/G]CCTTGAGAATTCACT	8925
rs553147056	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63736359	TGTTCATTCTGAATA[C/T]TGAGACTTCTAAACT	8925
rs553151853	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63826698	TTCATTTTCAAGCTA[A/T]AAGAACCAACCATCT	8925
rs553175461	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63720940	TACCAAACAACAAAG[A/G]ATGTTTCCACTATTC	8925
rs553189574	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63825888	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC	8925
rs553191178	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63806365	AAGGTGACTTCTTCC[A/G]TGAAGCTTTTCATGT	8925
rs553198514	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63614818	GAACAAGGATAACTC[A/G]AATGAAATAGAAAAT	8925
rs553214252	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63728412	GCAGAGAAGGTCATT[C/T]AGAAATGAGCTCAGT	8925
rs553215193	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63800785	GCATCTTTTGTTATT[C/T]GTAACAAGCCCCTTT	8925
rs553217629	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63765281	CCAGCCTGCTTACCC[A/C]CTTTAAATAGTGAAG	8925
rs553231075	snp	A/G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63814866	TCAAAATTGTTAAGA[A/G/T]GATCAAATAAGAATT	8925
rs553244007	snp	A/G	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63693044	AAATTAGATGGGTGT[A/G]GTGGCACACGCTTGC	8925
rs553245610	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63700973	AGAATCTGTATTTAG[A/C]CTTAACTTACAAATG	8925
rs553253659	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63684900	TGTAGTCCTAGCTAA[C/T]TGGGAGGCTGAGGCA	8925
rs553258707	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63833490	AGACGCGACCACAGC[A/G]GGGCCGGGGCACAGA	8925
rs553272963	in-del	-/A	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63672837	ATGAAAGATTGACAG[-/A]AAAAAATATTCTTAC	8925
rs553276795	snp	G/T	0.0134861	0.0810011	intron-variant	HERC1	GRCh38.p7	15:63737375	TATCTTTTTTCCAGA[G/T]ATATATATATATATC	8925
rs553298597	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63715058	AGAAATCAATTAAAG[C/T]GGTTAAGAGAATGGT	8925
rs553330359	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63787659	AGTCCTAGCTACTTG[C/G]GAGGCTAAGGCAGGA	8925
rs553346672	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63748234	CCATCTCAAAAAATA[C/T]ATATATACATATATA	8925
rs553349951	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63809474	TAAGCAATTACAGTA[C/T]AATATGATAATGTTC	8925
rs553375074	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63616848	AAAATTCAGTTCTTC[A/G]GCTTCCCTAATCACA	8925
rs553384973	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63809965	TACAGGTGTGAGCCA[C/T]TGCACCCAGCCAGGA	8925
rs553390197	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63794163	ATCATCAACATATAA[C/T]CATAAAAATGAGCAA	8925
rs553397856	in-del	-/A	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63776649	TCAATACTGGTGTGG[-/A]AATACACAGGTTGCG	8925
rs553400329	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63610222	CCTAGGTAAGCCACA[C/T]GTCCTGCTATGGGAG	8925
rs553405862	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63749953	TGTTACAGCGATTTA[C/T]CATGCTGCCTTTAGG	8925
rs553425070	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63764696	GTGTTACAACCCCCA[C/G]CACCAGGTATGTCAG	8925
rs553443427	snp	A/C	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63678794	CACAATCTGGATACA[A/C]ACTGCAAATAAGACA	8925
rs553476502	snp	A/G	1.65638e-05	0.00287778	missense	HERC1	GRCh38.p7	15:63630554	ACTGCCACATCTTCT[A/G]TGATTACTCCAGCCA	8925
rs553503595	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63697567	TCAAGTGATTCTCCC[A/G]CCTCAGCCTCCCAAG	8925
rs553534548	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63666291	GCCTCTTAAAAGTTA[C/T]GTTGTCTTTAATAAG	8925
rs553535755	snp	A/G	0.00636936	0.0560724	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834073	GTGAAAGGGGAACCG[A/G]GAGGAAGGCGGCTGA	8925
rs553546700	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63622657	ATCTTTGACAAGAGG[A/T]TAACAACAATATTTA	8925
rs553549979	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63651775	TGGGCGTAGTGGCTC[A/C]CATCTGTAATCCCAG	8925
rs553555471	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63625221	TTTACTTTATTTCCC[C/T]GACCTCCCTTTCCCC	8925
rs553559543	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63666712	TGTAAATAACCCACT[A/C]CTCATCCAAGTTCCA	8925
rs553562258	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63809141	GAAAGAGTTAATGGT[A/G]TCAAAAGAAATAGGG	8925
rs553576218	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63767567	GCCGGGCGTGGTGGC[A/G]GGCACCTGTAGTCCC	8925
rs553582138	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63822824	TGATCAGATTAGAAA[A/T]GTATTCAGAAAATAG	8925
rs553591632	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63744363	CTATTGCCTATGTTC[A/G]CTCAAGACTCTGTGG	8925
rs553599732	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63785367	TCAAAGCTGTGAGCT[A/G]TAAGTGCACCACTGC	8925
rs553625665	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63743869	GTGTGGATGCCAGTA[A/G]ATATTGAAGAGTTAG	8925
rs553627198	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63610825	ATGGGCCCTGCTCAG[A/C]GAACTGCCCAGCTCA	8925
rs553633920	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63782601	TAAACACAACATCCA[C/T]TCTGCAGCACATGGA	8925
rs553642679	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63696733	AGCTCACAAGGAGAT[A/G]TATGTGAAGGTTTCA	8925
rs553662427	snp	A/G	0.0138799	0.0821421	intron-variant	HERC1	GRCh38.p7	15:63742951	AGTTTTTCTTTTCTT[A/G]CAATGTTTTGGTCCA	8925
rs553696578	snp	G/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63710328	CTAAGGAGCAAAACT[G/T]GAAAAAGTAGGGGGA	8925
rs553708188	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63627860	ATCTTTGTGTAGCTA[C/T]ACAAAAATTTCATAA	8925
rs553711152	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63785386	GTGCACCACTGCACT[A/C]CAGCCTGGGCAATAA	8925
rs553711237	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63755721	AGGAAATCAAAGATG[C/G]AGTGGGCTGAGATAG	8925
rs553711302	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63617419	ATCATTGTTGGACAT[C/T]TGGGTTGGTTCCAAG	8925
rs553720014	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63796560	AGTTTATTTTGCCAA[A/G]GTTAAGGACATGCCT	8925
rs553724464	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63790406	ACACAGTGAAACCCC[A/G]TCTCTACCAAAATAC	8925
rs553735087	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63823875	TGAAAACGTAGCCTA[C/T]GGATTTGGAGAAAAT	8925
rs553735314	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63717613	AATCCTAGCATTTTG[G/T]GAGGCCGAGGTGGGT	8925
rs553736526	snp	A/T	1.68349e-05	0.00290123	intron-variant	HERC1	GRCh38.p7	15:63660940	GATATATAAAAAAAC[A/T]TGTAAAATAAAGAAG	8925
rs553741998	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63750747	TACCAGCCTGGACAA[G/T]GTGGCAAGACCCGAT	8925
rs553746407	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63746010	TCTCCTCAATTGTTT[G/T]TCTGTTCTTTATTTT	8925
rs553748537	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63796617	GACATGTACCCAAGG[G/T]GGTCAGGGACAGCTT	8925
rs553765373	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63733461	AGATAAATAATATGA[C/T]ACATGATTCTACAGT	8925
rs553766635	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63762033	TTTCTAGCACCCTGA[C/T]TGTGGTCTTGAAATA	8925
rs553772706	snp	A/G	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63619726	GTTTAGTCTTGGGAG[A/G]GTGTATGTGTCGAGG	8925
rs553786171	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63787940	TACTCCAGTCTTGGC[A/G]ACAGGGTGAGACCCT	8925
rs553790697	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63815857	TACAATCATGGCAGA[A/G]GGGGTTAGCAAACAC	8925
rs553790798	in-del	-/A	0.0032402	0.0401198	intron-variant	HERC1	GRCh38.p7	15:63645701	AAATGGAAGGAAGAG[-/A]AAAAAAAATCAGAGT	8925
rs553803449	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63753208	CAGATATGAAAAGCT[A/G]TGTTTCTGATAGCTG	8925
rs553807844	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63711159	GGCAACAGAGCAAGA[C/T]ATAAAAATTTAAAAA	8925
rs553838704	snp	A/G	0.000886873	0.0210393	intron-variant	HERC1	GRCh38.p7	15:63635921	TTCAACAACTAGTAT[A/G]TTTACAATGAAAGGC	8925
rs553859492	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63765346	TGTGTAAACCAAAAA[G/T]AAAATTCAAAGGCCC	8925
rs553862275	snp	G/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63621976	TGATCGTCTGAAGCC[G/T]TCTTCTCTCAACTCG	8925
rs553883477	snp	A/G	1.69824e-05	0.00291392	intron-variant	HERC1	GRCh38.p7	15:63616404	GACGTCAACACCAGT[A/G]GAAACATAGACTGGC	8925
rs553885393	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63642934	AGCTTACACCCTATC[A/T]TTTGATATAACTACA	8925
rs553888585	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63626985	AGGTCACTCAGATCA[C/T]ATGTGGAGGAGCTGG	8925
rs553893889	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63830291	AATATGATGCATTGA[A/G]AAGGACACAACATCG	8925
rs553927202	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63740935	TTTTGATGATGTCCA[A/G]TTTATTTTTCCTTTG	8925
rs553946519	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63724977	TACATTCTGGGAAGC[A/C]GTTTCATAACCTCCA	8925
rs553951350	snp	A/G	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63719964	TATTTGATGCCATAA[A/G]AGTATATACTGTGAA	8925
rs553958968	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63746463	ACTCTCCTTATTTAT[A/G]ACCAGTATTCTATTC	8925
rs553960244	snp	A/G	5.24159e-05	0.0051191	intron-variant	HERC1	GRCh38.p7	15:63690529	TCTTCTAATAATTTT[A/G]AAAATAAAAACCTGG	8925
rs553981324	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63771023	GTGAAACCCCGTCTC[-/T]ACTAAAAATACAAAA	8925
rs554021340	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63823218	GTCCATGTTTTCTCA[C/T]CATTTAGCTCCCACG	8925
rs554038031	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63763995	GGTGCCACTTCCTTT[C/T]GTAGCTTTTCCAGAG	8925
rs554041841	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63712500	GTTCACTTGTAGATA[A/G]GTTAAGATTGGGGTA	8925
rs554068940	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63662650	GCAATGTGAGCACAG[C/G]AGCCATGTTATATAA	8925
rs554088114	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63628569	GTGGCAGAAGGCTTG[A/G]TGGTTTCACAACGAT	8925
rs554102362	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63630727	CATTTAGCTTATTAT[A/G]GTGGAATGGCAATGA	8925
rs554108227	snp	C/T			missense	HERC1	GRCh38.p7	15:63747752	AAGGGAGTGGGGGAA[C/T]CTCACTGTTTATTTT	8925
rs554121461	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63773705	CGCACCACCACACCC[A/G]GATAATTTTTGTATT	8925
rs554132475	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63818103	TTACTCTTATTTGCA[A/T]GTCTGTTAACAATAT	8925
rs554146012	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63753896	AAAGATACTCATGCC[A/G]GGCACGGAGGTTCAT	8925
rs554155972	snp	A/C	1.84069e-05	0.00303366	intron-variant	HERC1	GRCh38.p7	15:63634914	ACCAAGGAGAAAGAA[A/C]ATTTTTAAGAAGGGA	8925
rs554157406	snp	C/T	1.74567e-05	0.00295433	intron-variant	HERC1	GRCh38.p7	15:63729661	GATCCTAAAATGACA[C/T]ACAAAGGAAGTTTAT	8925
rs554177245	in-del	-/GTGT	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63742381	AATAGTTGTGTATGA[-/GTGT]GTGTGTGTTCCTTAG	8925
rs554216442	snp	A/C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63610638	ATAATCCTTCCTGCA[A/C/T]GTGGCTTCTCCAGCA	8925
rs554225414	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63683209	TAACTTCATAAATGC[C/T]AAAGTTTCATCCTGA	8925
rs554255516	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63750955	AATAAAATAAAATGA[C/G]AACATATATTTGTAC	8925
rs554266222	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63816259	TATGTACTTGACATT[C/T]CAAGAGAGAATAAAG	8925
rs554284756	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63642205	TAGGGAATAATGTTA[C/T]ATCATAGAATTACTT	8925
rs554287804	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63820612	ACTTTAAAAAGCCTT[A/C]CATAAATACTACTGT	8925
rs554295731	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63777010	TATACACACAAAATT[G/T]TTAATTACAAAATAT	8925
rs554315120	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63625071	CTGTTTAGTGCTGCA[C/T]AGGACTCTGCTGCCT	8925
rs554320192	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63776604	GACTGTGAGGAGCAT[A/G]AGGACACTTCTTGAG	8925
rs554326085	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63784644	ACAGAGTCTCACTCT[G/T]TCACCCAGGCTGGAG	8925
rs554333456	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63658461	TTCTAAAATTCTATC[G/T]CACCCTCCCAAACAC	8925
rs554376803	snp	A/C	1.65723e-05	0.00287852	synonymous-codon	HERC1	GRCh38.p7	15:63661773	AGAACTTGTTGACTT[A/C]GATTTGGTCTTCATG	8925
rs554392544	snp	A/C/T			intron-variant	HERC1	GRCh38.p7	15:63721450	AGAATCGTTTGAACT[A/C/T]GGAAGGCGGAGGTTG	8925
rs554429475	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63624330	GGGATGTGCTGTTCT[C/G]TAACAGAAGGTACGG	8925
rs554434147	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63769665	TCGAGACCAGCCTGG[C/G]CAACATGGTGAAGCC	8925
rs554442428	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63669975	ATAGATGAAAAATGC[C/T]TGCCTTCACAGAGCT	8925
rs554442438	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63804823	ATAAACAGCCAAAAA[A/C]GCGCATGAAAGGATG	8925
rs554490717	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63631219	TCCAACCAACCTCTC[A/C]CCTTACCTTGCCAAA	8925
rs554496994	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63820679	AAAAGCAACAGAGAC[A/G]TTATCCTTTTTTTTT	8925
rs554518086	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63676224	TGCATCTTAACCAGG[C/T]ATCATAAATCCTTTC	8925
rs554586856	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63788428	TGATTGTTTTAAGGA[A/G]GAATTCTATCATGAC	8925
rs554590317	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63766015	CTTGACAAAATAAAC[C/G]TAAATTGATTTGCGA	8925
rs554610852	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63722637	TGATCTACTGCTGCG[A/G]TATCACAGTGATTGT	8925
rs554619796	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63794102	GGAAGTCACCCTATA[C/T]GGTCTAAAAAGGGGA	8925
rs554636406	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63693499	TCCACCCACCTTGGC[C/T]TCCCAAAGTGTTGGC	8925
rs554652937	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63715314	CAGATGACTATCATT[C/T]TTTTATTGTAATTGA	8925
rs554653373	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63738397	CAAAATTTCTAATAA[C/G]ATGTTTACTTAATAG	8925
rs554653803	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63679030	AAAAAAGGTTAACTG[C/T]TATTAGTATTGTGTT	8925
rs554680191	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63785928	CCAGGCTGGTCTCAA[A/G]CTCCTGGACTCAGGC	8925
rs554680577	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63751616	ACAGAAGAGGCCTGA[A/G]AGTGCTGAGACAGAC	8925
rs554684403	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63787049	GTTTCACCATGTTGG[C/T]CAGGCTGGTCTTGAA	8925
rs554697001	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63782800	GAAAAGGCCAAAGTA[C/T]CAATATTAACAAGAG	8925
rs554699561	snp	C/T	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63826012	AGGTGATCCACCCAC[C/T]TCAGCCTCCCAAAGT	8925
rs554709267	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63616309	GCAGCAATGGCATAG[A/C]TATGGCATTGTTCAG	8925
rs554713855	snp	G/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63716117	ATATGTAACCCAAAA[G/T]CATCAGAATAGTACT	8925
rs554721112	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63779937	GAGAATCGCTCGAAC[C/G]CGGGAGGTGGAGGTT	8925
rs554732804	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63801530	AAAGACAATCTTTCA[C/T]ATTAGTCTATAAAGA	8925
rs554738635	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63665699	TACACAAAAATTATG[A/T]AATTTCTTCTGGCAT	8925
rs554754749	snp	C/T	8.67491e-05	0.00658536	intron-variant	HERC1	GRCh38.p7	15:63723158	CTAACTACAAATTTA[C/T]TCCCTTTATCTTCTT	8925
rs554768274	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63708036	ATACATGTACCCCTG[A/G]TGCAGATAAACACAC	8925
rs554769685	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63794941	CGTGGTGGTGTGTAC[C/T]TGTAGTCCCAGCTAC	8925
rs554771921	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63611046	AGGAGATGACTGGCA[C/T]TGGGCTTATAGGATG	8925
rs554791322	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63681822	TTCTTGCTGGGGAAA[A/G]CTTGTGCACTTGTGC	8925
rs554805812	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63821134	AGCTTAAGAATTACT[G/T]GAACTAGCCAGGTGC	8925
rs554818922	in-del	-/CT	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63784367	AATCTCCAAGATACA[-/CT]GTTAAAAAAGAAAAA	8925
rs554819994	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63789176	GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC	8925
rs554820415	in-del	-/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63676317	CTGGTTTCTTAGCTT[-/G]GTAGAATGGAGGGGA	8925
rs554837481	snp	G/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63807488	TTTTCCCCTCAGACT[G/T]AAAAGTGTACTAATG	8925
rs554860457	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63782146	CTACCTAAGGTAACT[C/G]ATGAAAGTAGTTATA	8925
rs554868462	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63672354	CCAAATTCAGTAAAA[A/T]GAGCTTGACTATATA	8925
rs554886364	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63815186	CTTATGGCTCTGATT[A/G]TCTAAAAGTTAAATA	8925
rs554917974	snp	A/G	0.000399281	0.0141238	stop-gained	HERC1	GRCh38.p7	15:63656216	GCCCACCTCGTGATC[A/G]TTCTGAGGTGCTAGC	8925
rs554937852	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63745150	CAAAGTCCTGCCCAC[C/T]CTTCCCTCTCAAGTG	8925
rs554953267	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63702822	TAGAAGTAAATTTAG[C/G]TGGCCGGGCATGGTG	8925
rs554955501	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63803385	CACTAAATCATGCTG[C/T]TTCTTATCAACATCG	8925
rs554956577	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63655434	GTACTGATAAGTAGT[C/T]CCTTCAAAGTGTTAT	8925
rs555003029	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63659061	ACTGAATTACCAATA[C/G]TGCCCAATTCTTTAT	8925
rs555005262	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63646131	GCTGTGATCATTGTG[A/C]TCTTCTGATTTTATT	8925
rs555006142	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63639902	AAGAAAATGAGAAAA[C/T]ATGGGACTATGTCAT	8925
rs555042929	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63695312	AAAGTGCTGGGACTA[C/T]AGATGGGTGCCACCA	8925
rs555049093	snp	C/T	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63743085	ATATTTTGTGGAATT[C/T]ACAAGTGAAGCCATT	8925
rs555050313	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63801956	TCAGATGTACCAAAG[C/G]AATCTCTAACACATC	8925
rs555056439	in-del	-/AA	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63708982	TAAGGAAAGATGATC[-/AA]AAGTCAATCTGGTGT	8925
rs555076433	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63747493	TCAAGTCATGAACAA[C/T]AGTAATTTTTAAAAC	8925
rs555088747	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63735277	GAGCACACAAACAGG[C/G]CAATTAACATGGCCT	8925
rs555118977	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63699466	CAAAGTGTCTACATA[C/T]CTGCAATGAAACATT	8925
rs555132791	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63648531	GGACCAAAATCTACC[A/G]TGAAACTGAGAAGTG	8925
rs555140963	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63615205	AGGCAAGGTCTGAAT[A/G]CCAGATGAAAACAGT	8925
rs555168706	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63822455	GCCGGGCGTGGTGGC[A/G]TGTGCCTGTAATCCC	8925
rs555182678	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63705034	TGAGCCACGACACCC[C/G]ACCCTCTGTAATTTT	8925
rs555186350	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63786225	TATGATTGTGCCTGA[A/G]AATAGCCACTACACG	8925
rs555187871	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63828618	TGCTGGGATTACAGG[C/T]ATGAGCCACCGCACC	8925
rs555230190	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63688023	TGGAGTATTTTAAGC[A/C]GGGGATGAACATGCT	8925
rs555251545	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63785447	TATATTAATAATTCA[A/G]TTCAAAATTAGAAAA	8925
rs555269997	snp	C/T	0.0103295	0.0711199	intron-variant	HERC1	GRCh38.p7	15:63616918	GTTTCACACAGCACA[C/T]GGACTATATTCTGAA	8925
rs555274391	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63643690	CTCATAAAGGATAGT[A/G]AGCTTGACTGAATCA	8925
rs555305632	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63698176	ATCTCAGCACTTTGG[A/G]AGGCCGAGGCAAGTG	8925
rs555319857	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63649125	TTTGGGAGGCCAAGG[C/T]GGGCGGATCACAAGG	8925
rs555325055	snp	A/G			synonymous-codon	HERC1	GRCh38.p7	15:63694439	TGTCTGTACCACACA[A/G]CTGTGACAATACGTT	8925
rs555335954	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63812288	CTCTTAAATCTTCAA[A/C]CCACATTTCCATTGT	8925
rs555358523	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835333	AAAATGTGTATTTCT[A/G]GTAAATGATGTAAGG	8925
rs555363532	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63705846	ACCAGCCTGGGCAAA[C/T]AGGGAGACCTTATCT	8925
rs555364070	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63769369	GAGCTGCAGTGAGAC[G/T]AGATCTTGCCACTGC	8925
rs555397528	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63804244	TTAAATAGCACACAA[C/T]AAATTGATAAGCTAG	8925
rs555398525	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63698518	TGAGTATATTGTTCT[A/G]AGAGATGACAATTTT	8925
rs555419737	in-del	-/AAAAAATAAA	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63809224	TTTAACCTCTTCATC[-/AAAAAATAAA]CAAAAATAAAGGCAT	8925
rs555444018	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63677038	TTTTGGAATATTTAC[A/G]TTGTACTTAGCAGGT	8925
rs555447769	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63622614	CTGGAATTACAGGCG[C/T]AAGCCACCATGCCTG	8925
rs555470043	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63663613	GCACATGCCACCATA[C/T]CCAGCTAACCGTTTT	8925
rs555472829	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63755135	CAAAATAAATGACAG[C/T]CTTTGGCCTAGTAAA	8925
rs555482365	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63720729	CCATTCCATGGAATT[C/G]CTTGCTATTCTGAGA	8925
rs555491799	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63700133	GTTTTAATGTATTCC[G/T]AAGATGAATAATGGT	8925
rs555500493	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63705100	TCTCAAAAGACTTCT[C/T]GATAAAGAAAGCTCT	8925
rs555517933	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63727489	TTCCAATAAAATAAG[A/C]GGACTTACTTAAATT	8925
rs555537819	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63818976	AATTTATGTAAAACG[C/T]CTAGGCTTTTGGTAT	8925
rs555556678	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63818303	CAGCAGAGTTACTGC[A/G]TAAAGCACTCCGGCT	8925
rs555562208	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63779080	AGTAGACTCAATGAC[A/G]TAAAGAAAAATGAAA	8925
rs555581845	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63735383	TGAACATCACACACC[A/G]GGGCCTGTTGTGGGG	8925
rs555596140	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63770209	AAAAGTTCTCCAGCT[C/T]CCCTGACACACACAC	8925
rs555603337	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63771545	AAGCGATTCTCCCTG[A/C]CTCAGCCTCCCAAGT	8925
rs555610528	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63806229	AGAGTGCAGTGGCTA[C/T]TCACAGGTGCAGTCA	8925
rs555618523	snp	C/T	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63734673	TATTTCCTTCTCAGT[C/T]CAAATTTTTAGGATA	8925
rs555631003	snp	A/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63707356	TAAATGTCTTTTTAA[A/T]AAACCTATTACAATA	8925
rs555634641	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63766921	AACCCCAGGTGATCT[A/G]CCCACCTGGGCCTCC	8925
rs555637152	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63609655	CAGCTGCAGGGATGC[C/T]CCCACAGAGCAGGTA	8925
rs555653363	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63741474	CACGCCACTACACCC[A/G]GCTAATTTTTTGTTA	8925
rs555654077	snp	C/G	0.000946384	0.0217324	intron-variant	HERC1	GRCh38.p7	15:63749811	AAAAAACAGAAATAC[C/G]TTACACATAACTTCC	8925
rs555679740	in-del	-/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63794037	GGTTGTCCTCACTGC[-/T]TACACTCCCATCAGC	8925
rs555690788	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63825520	AAATAAGTAAGTAAG[C/T]CTGAAATAAACAAAT	8925
rs555693355	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63820154	AATACATGAAACTTC[C/T]TAGAACAGTGACTGC	8925
rs555703834	snp	A/G	2.05396e-05	0.00320459	utr-variant-3-prime, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609065	GAGAGAAGGGAGGGT[A/G]AGAGCACCCGCACGG	8925
rs555713424	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63716889	CTGCATAAATGTTTA[A/G]TAATTCTAAATTTAA	8925
rs555719858	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63815091	TCCCCTAGAAGTATA[A/C]CTTGTTTTATGGATA	8925
rs555726420	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63788376	ATAAATCAGTAATGA[C/G]ATTTAAAGAAACTAT	8925
rs555727094	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63793739	TCTTGGGGTCTGGAT[A/G]GGGACCCCTTTCCAG	8925
rs555732427	in-del	-/ATAC			intron-variant	HERC1	GRCh38.p7	15:63660350	TAAATAAATAAATAA[-/ATAC]ATACATACATACATA	8925
rs555748578	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63830983	GCTTTGCAAACTTCT[C/G]TGTAAATGATTTGAC	8925
rs555758608	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63815680	GTCAAACACACTCTT[A/C]ATGGTTGGATATATT	8925
rs555789448	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63639091	AAACTCTTTGTGTAG[C/G]TGTGGGCAAATTACT	8925
rs555792438	snp	A/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63800253	CAAAGGGGAAGAGTT[A/T]AAAATTTTTCTGAAG	8925
rs555796115	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63670174	AAGTTATGGAAAGAA[A/T]AGGTAACTGTCTAGT	8925
rs555816617	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63770683	TAAATACAATTTACC[A/G]ATTGAACTTATTTTT	8925
rs555818165	in-del	-/ATAT			intron-variant	HERC1	GRCh38.p7	15:63772508	TATTTTATTGTTTTA[-/ATAT]ATATATATTAAATAT	8925
rs555818617	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63622129	AGTATGTAATTGCAA[A/G]TACTAAATTTTGTGA	8925
rs555829441	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63687338	AGGTCAGTAGTTTGA[C/G]ATCAGCCTGGCTAAT	8925
rs555844414	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63681167	ATATTAAGCCTGAGA[A/C]TAGGTGTATTGTTTT	8925
rs555881091	snp	C/T	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63821982	GTAAAGCAAGAGAGA[C/T]AGGGGATGTAGGGAG	8925
rs555900477	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63625484	GGATCATTTGAGGTC[A/G]GGAGTTCGAGACCAG	8925
rs555903760	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63613323	TAGTGCTGGGCACAG[A/G]CAAGTTGGGGAGTGC	8925
rs555904683	in-del	-/AAAC	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63646814	CTCCATCTCAGGAAA[-/AAAC]AAACAAACAAACAAA	8925
rs555915785	in-del	-/TTAA	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63706696	TATAAAAACAGCTTC[-/TTAA]TTTATTTACTATGCT	8925
rs555938738	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63728181	GAAATATTTATTGAC[A/C]TACCAGGCACAGTTC	8925
rs555948391	snp	A/G			missense	HERC1	GRCh38.p7	15:63640216	GTAAAAGATTCTGGA[A/G]ACTGGGCTCCATTGG	8925
rs555950633	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835350	TAAATGATGTAAGGG[A/T]GTAGCTACATGAGGA	8925
rs555959517	snp	C/T			synonymous-codon	HERC1	GRCh38.p7	15:63758325	AGTCTGAATGCTATC[C/T]GGGCTAGCACATGTT	8925
rs555982603	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63664174	ATGCATCATCACTTC[G/T]TAAATTATAATTGAC	8925
rs555993080	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63799603	AAGAAAATTATGATC[C/T]CCATGGGTAGTAGTG	8925
rs556013614	snp	C/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63699330	TGCAGTATTAAACCA[C/G]ATCATCATTTATGAA	8925
rs556014326	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63657426	TTTCATGTTTATTGG[C/T]CATTTGGAGATCCTC	8925
rs556021815	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63616765	ACAGCTATAGCGTTA[A/G]TCTATACCTGTACTG	8925
rs556031546	snp	A/C/T	0.000177289	0.00941346	intron-variant	HERC1	GRCh38.p7	15:63723389	TTACCAATTTTAACA[A/C/T]CATAAATTTTGGTGC	8925
rs556051462	snp	A/C	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63656911	ATTGACATATACATG[A/C]AATCTGCCACAGTTC	8925
rs556060931	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63748501	CATATTAAGAAAAAT[A/G]TCCTGACTCTATAGA	8925
rs556072952	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63709600	AAAGTCCATGGTGAG[C/T]TTTAACCCTATTCTG	8925
rs556075335	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63626312	AGTTTGGTGTGTGCA[C/T]TTGTGTTGGTTTTTA	8925
rs556079407	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63797374	CACTTCCTCAATTAC[C/T]CTTATAGAGAAAATC	8925
rs556092370	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63757106	TATGGCAAGAACCAT[A/G]TAAAATGTATTCTAA	8925
rs556094270	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63765147	CTCTCTGTTCACCTT[A/G]TCTTATATAAAATGC	8925
rs556099487	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63634025	CCTAAAACACACTCC[C/T]CCGTTTCTGGGACCC	8925
rs556116385	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63666663	CATTTATGTTATACT[C/T]TGTAAAGATTTGTGT	8925
rs556131070	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63758016	CCCAGCAAAAATTTA[C/T]TTTTCTATTAAAATG	8925
rs556132486	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63724257	CACAAGGTTAAACAC[C/T]GACAGCAGTGGAATT	8925
rs556148616	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63657456	CTTTTGTGAAACACT[G/T]CTTAATGTGTTTTGT	8925
rs556154502	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63732253	TGATCCACCCAACTC[A/G]GCCTCCCAAAGTGCT	8925
rs556155002	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63673709	AATATCTCTGAGAAG[A/C]TATCAGAATACTATG	8925
rs556162114	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63619663	CTATTAATTATTGCC[C/T]CAATTTCAGAGCCTG	8925
rs556195110	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63739601	CCCAGCACTTTGGGA[A/G]GTCGAGGCAGGCAGA	8925
rs556208778	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63632457	AAAAGAAGAGGGGAC[A/G]GCCCTTGGCAGGGAC	8925
rs556210423	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63781993	AAGGCTGAGAGAGGT[A/C]AGGAAAATGCAGAAG	8925
rs556217385	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63752571	TATTTTCCATACCTA[A/T]GTGTTCTCTTTACCC	8925
rs556242220	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63738208	AAAATGACAGAGATA[C/T]TCAATAAAATAATTA	8925
rs556243484	snp	C/T	3.31285e-05	0.00406978	missense	HERC1	GRCh38.p7	15:63774989	ATAGGAGGAATCTTG[C/T]TTTCATTTGCTAATG	8925
rs556269903	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63731580	ACATCAGATTAAATT[C/T]ACATTTTTAAATCTG	8925
rs556284130	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63703425	ATTGTCATTTATACA[C/T]CCATTAAACTTCAGT	8925
rs556288224	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63776510	TCCTCTTCTAAAGAT[G/T]TATCCAAAAGAAAAC	8925
rs556294234	snp	A/G	3.32856e-05	0.00407942	missense	HERC1	GRCh38.p7	15:63753037	CCTTGTAAAGCTTCA[A/G]TAACTTTAGGTTTAT	8925
rs556299532	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63762860	ACTGAGGCAGGGCTT[A/G]CATAATGTCCTCTCG	8925
rs556309301	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63793507	CCTCAGTTTCGGGAA[C/T]TGCCCACCCCTCTCC	8925
rs556316806	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63745854	CTCAATTTCCCTTTT[G/T]ATTTCTGTAGGGTCA	8925
rs556319079	snp	A/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63803009	GAGCCCAGGAGTTTG[A/T]GACTAGCCTGGGTGA	8925
rs556320297	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63631847	CGCCCGGCCCTCCCA[A/C]GTCTTATTCCTGTGC	8925
rs556332212	snp	C/T	1.65748e-05	0.00287874	intron-variant	HERC1	GRCh38.p7	15:63661031	TCCCTTGTACCTGCA[C/T]CAAACATGAAGAACA	8925
rs556337937	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63746378	TTTGTATTACAAATA[G/T]ATAGATATTTTTAAG	8925
rs556343157	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63640625	GAGGATTTCTGTATA[C/T]CCTTCGCCCAACTTT	8925
rs556351310	snp	C/T	0.00636936	0.0560724	intron-variant	HERC1	GRCh38.p7	15:63789658	CAAAAATTAGCTAGG[C/T]GTTGTGGCGGGCACC	8925
rs556354316	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63796993	CTTTCCATCATGGCC[A/G]GAACTAGTTTATCAG	8925
rs556359269	in-del	-/AGG	0.00398564	0.0444627	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834928	TCCAATTGGAGGCGT[-/AGG]AGAAGCACACAAACA	8925
rs556371763	snp	A/C	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63653708	AACAGAATGTAAATA[A/C]TATGTAAACAGTTAT	8925
rs556378103	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63809282	AATGAACCAAGGGTC[A/T]GTCCTATTTGTACAT	8925
rs556407939	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63660330	ATCTCAAAGAAATAA[A/G]AACAATAAATAAATA	8925
rs556427342	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63627759	AAGGTAACAGCTACA[A/T]CTGGAAGGAATGGAA	8925
rs556453253	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63719248	TATTTTATATAAGGT[A/G]GTCTGGGAAAGTTTC	8925
rs556489135	snp	C/G	4.51579e-05	0.00475152	intron-variant	HERC1	GRCh38.p7	15:63634719	CTAGAATATCTTATT[C/G]ATTTATTCCATGCCT	8925
rs556489887	snp	C/T	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63812876	GATTCGAAGACTAAA[C/T]ATTATAAAATGTCAA	8925
rs556495260	snp	C/T	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63707156	CTTATTAGCACCTTC[C/T]GGATGCCTAAAGCCT	8925
rs556500137	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63715960	CCTCACCGCTCAGAC[A/G]TCTTCGAGGCTGGTG	8925
rs556506896	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63829380	GTAAGCTATGATCAC[A/G]CCACGGCACTGCAGC	8925
rs556510498	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63676088	TGTATTTTTAGTAGA[A/G]AGAAGGTTTTGCCAT	8925
rs556520063	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63736597	GCATCCATCAGTCTT[C/T]TAGCATCACACTCTC	8925
rs556523267	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63641717	CACCATTTAATCTGC[A/G]AAATTCCTTCTAGTA	8925
rs556528679	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63761884	TAAGTAAAAATTCTA[C/T]AGCTGTGAATTTGAA	8925
rs556539066	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63823829	TTAAAATGAGAGACA[C/T]TTCTGCATAGCAAAA	8925
rs556543612	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63823012	ACCTTCTGTGTTGTA[A/C]AAATTTAGTTTGAGA	8925
rs556558725	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63742697	TGTTGAATTTTGTCA[C/G]ATGCTTTTTCAGCAT	8925
rs556562711	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63644589	CTAGAGGGCTCTCTA[C/T]AAATATATACATTTG	8925
rs556597340	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63742237	AAGTATCCTATTCTT[C/T]TTGATGCTTTTGTAC	8925
rs556631298	snp	A/T	0.00636936	0.0560724	intron-variant	HERC1	GRCh38.p7	15:63733864	CTCAAAAAGAAAAAT[A/T]AAAAAATCACCTATG	8925
rs556636115	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63682638	CAAACAAACAAGAAT[A/G]GAAAGGAACTACTCC	8925
rs556641697	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63724378	CATGGCCAAAATCAC[G/T]TTCTGGTTCATAAAT	8925
rs556641794	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63696535	GCACACATCAGAATA[A/G]AAAAGGTTAGAGTAC	8925
rs556646516	in-del	-/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63654991	CCTTTAAGAAAACAG[-/T]TTTGGCTTTTGTTGC	8925
rs556654636	in-del	-/AAAT			intron-variant	HERC1	GRCh38.p7	15:63650374	CAAGACTCCGTCTCA[-/AAAT]AAATAAATAAATAAA	8925
rs556656191	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63647803	TATTATTAAAAAGAC[A/G]AAAAACAACAGATGT	8925
rs556671231	snp	C/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63688896	GGGGCTGGGGGAAGG[C/G]TTTGAGGGGGAGACA	8925
rs556687951	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63825959	GTAGAGACGGGGTTT[C/T]ACCATGTTGGCCAGG	8925
rs556690667	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63631113	CCTCCTGAGTAGCTT[C/G]GACCACAGGCACATG	8925
rs556722173	in-del	-/T/TT			intron-variant	HERC1	GRCh38.p7	15:63767007	TAGGTTTTTCATTTG[-/T/TT]TTTTTTTTTTTTGAA	8925
rs556727293	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63664380	GACTGAGCACTTAGT[A/T]TCATTAGTTTGAATC	8925
rs556742104	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63668464	CTCCAGCCCGGGTGA[C/T]AGAGCAAGAGGCTGT	8925
rs556743193	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63650068	GAATAAGACCATGAA[A/G]GCAGGATCCTTCATT	8925
rs556775233	snp	A/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63817195	TAAAGTATGAACCTT[A/T]TTTGGATGTCACTTC	8925
rs556778513	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63727229	TGCAATGAGGCAAGA[C/T]TGCGCCACTGCATTC	8925
rs556803364	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63776548	CATAAAAATACTTCA[A/G]TCAAAATAGTGGTTG	8925
rs556814068	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63810696	AATGGGAAAGCGTTG[C/T]AGGAGAGACAACTTT	8925
rs556828941	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63623183	CAAATCGAATCAGTA[A/G]TGATAGCCAACCATT	8925
rs556838192	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63651697	CTTATTTGCCTAAAC[-/T]TCTTGGGAATACTTC	8925
rs556885969	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63721836	CAGCCTTTGAAAATA[C/T]GTACATAAAATTAAT	8925
rs556897964	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63683108	GCCACTGCACTCCAG[C/G]CTGGGCAACAGAGCT	8925
rs556903539	snp	A/C/T	3.31391e-05	0.00407046	intron-variant	HERC1	GRCh38.p7	15:63645108	AGCCACTTAAAAAAA[A/C/T]TGATCACATAAAACC	8925
rs556911419	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63637009	AAACCGTCGGTGCTC[C/T]CTTTGTAGGCTTCAG	8925
rs556936195	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63735641	TGCATTATCTTAGGC[C/T]TCATAACTTCTCTGG	8925
rs556942207	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63650611	AATAGGGCAAAATGG[C/T]AGCGTTATAGAAGAG	8925
rs556952083	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63658382	AAGTATTAACTGAAT[A/G]ACCGATTGAGTGAAT	8925
rs556968638	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63794212	GTTCTGTCTATGGAG[C/T]AGCCATTCTTTCATT	8925
rs556976257	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63791880	AATTATCTGTTGGCA[A/G]TAACATCTCCTATAT	8925
rs557002268	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63699972	GGCCCAATTTTGAAA[C/T]CACATATTTATAATA	8925
rs557035201	snp	A/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63701114	TTTCAAAATGAATAT[A/T]AAATGCGCAAGGAAC	8925
rs557036461	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63685374	TATATGTTCTGATTA[C/T]AGGTGCCCTAATAAT	8925
rs557041780	snp	A/G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63750826	TGGTCCCAGCTACTC[A/G/T]GGAGCTGGGATGGGG	8925
rs557047093	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63831743	ACTATTTATTATTTG[C/T]ACCCTCTACTAACCC	8925
rs557049870	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63651853	CCAGCCTGGCCAACA[C/T]AGTGAAACCCTGTCT	8925
rs557065248	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63793267	GGCACAAGACACAGG[G/T]CGTAAAGACCACGCT	8925
rs557066917	snp	G/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63800062	TCCCTTGAGCCACAG[G/T]AGGTCAAGGCTACAG	8925
rs557073010	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63692269	TTAGAGTTTTCTTTT[C/G]ATCAAATAGGTACGC	8925
rs557073934	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63800889	TGCCAGAGAAACCAA[A/C]CAAGTGATAAAAGTG	8925
rs557109236	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63672261	ACTTGCTGGTCAGCA[C/T]GACAGCTGATTAGAC	8925
rs557165890	in-del	-/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63638290	TATATCATGACTTTC[-/T]TTTAATGATTCCTCA	8925
rs557173613	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63820494	ACCACTTATTTCCAA[A/T]GCTATCAGTTATCAA	8925
rs557181141	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63789140	CTGTCGCCCAGGCTG[C/G]AGTGCAGTGGTGCAA	8925
rs557190303	in-del	-/AT	0.00559996	0.0526177	intron-variant	HERC1	GRCh38.p7	15:63772508	TATTTTATTGTTTTA[-/AT]ATATATATATTAAAT	8925
rs557205477	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63794895	AAATGGCAAAATTCT[A/C]TCTCTACTAAAAATA	8925
rs557209999	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63813795	CATTTTGTCCAGGTA[C/T]GGTGGCTCGCGCCTG	8925
rs557242597	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63788357	TAGTTGGGATACTAC[C/T]GAAATAAATCAGTAA	8925
rs557243755	snp	G/T			intron-variant, downstream-variant-500B	HERC1	GRCh38.p7	15:63669168	CTTCCAAATAGTCCA[G/T]AGGGCAAAGAAGACA	8925
rs557264613	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63826404	ACTACCATACCATGG[G/T]TATCAATACGTACTG	8925
rs557330130	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63803659	ATTCAGTTCCTTCTT[A/G]AAAGTCTTGTTGCTA	8925
rs557330327	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63661552	ACACAGTCAAACTCC[A/G]GGGAAGGATATGTTG	8925
rs557361265	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63610926	GTAAGTTCTGGGTTT[G/T]AGGGCTGTACCCAGT	8925
rs557377651	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63690100	CCCAGGAGGCGGAGG[C/G]TGCAGTGAGCTGAGA	8925
rs557385996	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63743911	AGTCTTCACTGTCTG[A/G]GCTTATCTGTACCCA	8925
rs557396832	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834190	GCGGCCCTCACCCTT[C/T]AGCCGTCGCGGAATC	8925
rs557402349	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63668365	GGGTGTGGTGGCATG[C/T]ACCTGTAGTCCCAGC	8925
rs557406004	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63720197	CAGTCTCAAACCCCT[A/G]GGCTCAAGCGATCCT	8925
rs557408729	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63645957	ATTCTGACTCAAAAG[A/G]GATATGTTATCTCTC	8925
rs557422772	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63768771	CCATCCCTTACTGGC[C/T]CTTACTGAAAGGGTC	8925
rs557430589	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63718474	CATGTATTGAACATA[A/T]GCAATAACCAAGGCA	8925
rs557439222	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63667446	TCAAATGTCTACTGA[C/T]GAAAACTATAGTGTC	8925
rs557469124	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63829248	AAACAGCAGGACCTC[A/G]TCTCTACTAAAAATT	8925
rs557489801	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63707854	GAATCACTTGAACCC[A/G]GGAGGCGGAGGTTGC	8925
rs557534402	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63828032	ATGAAAGTGTTCCGG[A/G]ATTAGATAGTTGTGA	8925
rs557544333	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63805772	GGCAATACAGGGAGA[A/C]CCCATTTCTACAAAA	8925
rs557556056	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63646516	AAAAAAAAAAAACCA[A/C]GAAGGCTGGGCACCG	8925
rs557577866	snp	A/G	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63675268	CATTACAAACACAGA[A/G]AAAAACGAGTCTATT	8925
rs557579741	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63792243	AAGAACACATACCCT[C/T]TTCTCCAGGCCTCAT	8925
rs557603570	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63832052	CATTTAATCCATTCC[A/G]ATAACAACAACCCCA	8925
rs557604289	snp	A/T	0	0	intron-variant	HERC1	GRCh38.p7	15:63798219	ATTCAGCTCCCTGAT[A/T]GCAGGTTCTCCCCAG	8925
rs557607934	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63738269	AAGACAAAGAAAGAC[C/T]AAGGAATTGTTGCAG	8925
rs557608764	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63627598	AGAATCGCTTGAACC[C/T]GGGAGGCAGAGGTTG	8925
rs557624189	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63748881	CTGATGGACTAAACA[C/T]GTACAGTTAGCACTT	8925
rs557668164	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63830925	TTATGCTCTTTTTCA[C/G]TTTTTGTAGTTAAAG	8925
rs557679195	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63643242	TTAAAAACACTTATC[A/T]TCAGTAAGAAAAATG	8925
rs557697030	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63768158	CTGATTCTATTCGAC[C/T]GTTTCTCTTATTGCT	8925
rs557703469	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63754143	TGCATCACTGCACTC[C/T]AGCCTGGGTAACAAA	8925
rs557710491	snp	G/T	0	0	intron-variant	HERC1	GRCh38.p7	15:63818177	TATTTATTTTTAAAT[G/T]TTTTTTATTAAATAA	8925
rs557714244	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63665261	ATTCTAGGCCAGGAA[C/T]GGTGGCTCATGCCTG	8925
rs557717242	in-del	-/CT	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63795057	GGCAACAGAGCAAGA[-/CT]CTGTCTCAAAAAAAA	8925
rs557735263	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63654549	CTGTAAGAAATCTGA[C/T]TCATTAAAAATATAC	8925
rs557743260	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63818930	TTAAAAGATATTATA[A/G]TGCTGCCATTAGAAT	8925
rs557756377	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63783408	TCAGCATTTTTTAGC[-/A]AAAAAAAAAAGTATT	8925
rs557756600	snp	A/G	0.00199481	0.0315187	downstream-variant-500B, utr-variant-3-prime	HERC1, FBXL22	GRCh38.p7	15:63608450	ACGGTTCTCTGATAC[A/G]TTATTTCCAAGTGAA	8925
rs557769103	in-del	-/TCAA	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63676552	CTTGAGGTCAGGAGT[-/TCAA]TCAAGACCAACCTGG	8925
rs557786562	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63810029	AAATAAATTATACAC[A/C]TATACTAGAATTCAA	8925
rs557787069	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63705001	CCTCAGCCTCCCAAA[A/G]TGCTGGGATTACAGG	8925
rs557789181	snp	A/G	0.00636936	0.0560724	intron-variant	HERC1	GRCh38.p7	15:63739583	GTGGCTCATGCCTCT[A/G]ATCCCAGCACTTTGG	8925
rs557790827	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63617017	TTATCTTTTTTTTTT[A/T]TTATTATTATACTTT	8925
rs557819703	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63629099	AGATTACAGGTGCCC[A/G]CCACCACACCTGGCT	8925
rs557822762	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63787628	TATAGAGCCAGACTC[G/T]GTGGCACACATCTAC	8925
rs557867317	snp	C/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63620762	AATGGCCTTCTTTGT[C/G]TCTTTTGATCTTTGT	8925
rs557874802	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63727376	TTGGACTAAGTGACA[C/G]TTGATCACTGAACTG	8925
rs557885560	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63818052	TTGACATGAACTTCA[C/G]AAGTAATCAACATGC	8925
rs557894225	snp	A/G	1.77285e-05	0.00297723	missense, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609215	GGCTGGAGTACGGGG[A/G]CAGCCTCAGCTGGAA	8925
rs557897256	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63676916	ATTATGTAGAGTCAT[G/T]AGACAAATGAGTCTA	8925
rs557916032	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63733592	GCGCAGTGGCTCACA[C/T]CTGTAATCACAGCAC	8925
rs557928617	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63619795	ATAGAGGTGTTTATA[A/G]TATTCTCTGATGGTA	8925
rs557981156	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63784711	CTCCCAGGTTCAAGC[A/G]ACTCTCCTGCCTCAG	8925
rs558009644	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63615547	CCCAGGAGGCAGAGG[C/T]TGCAGTGAGCTGAGA	8925
rs558014089	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63734374	ATAGTCATCTATACT[C/T]TTTATACAAACGATT	8925
rs558019127	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63820482	TAAATTAGGTTAACC[A/G]CTTATTTCCAATGCT	8925
rs558036478	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63757009	ATTGAATGAAACAAC[A/G]AAGTAAAACGCTTAA	8925
rs558041085	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63767920	GAAGTTTAATCTTCA[G/T]TCTCTTCATATAGCT	8925
rs558043425	snp	G/T	0.000166339	0.0091182	intron-variant	HERC1	GRCh38.p7	15:63747127	TCGGATCATAAAAGT[G/T]CCTGTGCTATCCAGT	8925
rs558044982	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63791463	CAAGATTTGCCAAAC[A/G]TAAGGGATGATCTTT	8925
rs558058975	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63805560	TATGATGATTGTGGT[A/G]GTAGTTACATAACTG	8925
rs558062421	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63712603	ACAAGAGATTGAAAC[C/T]ATTAACACATATGTG	8925
rs558066755	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63720612	ATCCTGCTTTATCAG[C/T]AAAAAAAATTGACAA	8925
rs558067142	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63656876	CATCCAAATCTTGTA[A/G]CATTGAGCAGTTCGT	8925
rs558073473	snp	A/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63748321	TGATAAAACCTTTCA[A/T]TTTAGCAACTAAGGA	8925
rs558079832	in-del	-/GAGAA	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63654053	AACTTTGAGCTCCTT[-/GAGAA]GAGAAGAGACTATTT	8925
rs558088494	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63615039	ACAGCAGCAAGACAG[A/G]GAAAGGGAAATCCAT	8925
rs558103355	snp	C/T	8.56091e-05	0.00654196	missense	HERC1	GRCh38.p7	15:63723212	AGTCCTGCATGCTGA[C/T]CCAAAGGCTTCGGGC	8925
rs558107745	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63821254	GAGTGAGACCTCATC[C/T]CTAAAAAAATTAGCA	8925
rs558140311	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63722833	AAAAAACGTAATGTA[C/T]ATAAGGTACGGTACT	8925
rs558141977	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63770428	TGGGCTGTCTAAAGA[C/T]ATGGATGCTCCAAAG	8925
rs558144370	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63821910	AGTAAGGAAGACAAA[C/T]AATAACCAGGTAGGC	8925
rs558147223	snp	A/G	5.8755e-05	0.00541978	intron-variant	HERC1	GRCh38.p7	15:63628646	TGCTAAAAAAGAAAC[A/G]CTGCAGGAGCATGAA	8925
rs558173291	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63734452	TTTCAACTCAGCATA[A/C]TACAAATAAACCACA	8925
rs558198574	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63676270	AATGAGAGGAAAGGT[C/T]GACACTTGCATGTCA	8925
rs558198911	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63636825	GTCACAAAGAGGTCT[C/T]GAAGCTTGTGCAATG	8925
rs558268535	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63777205	GTTTCTTATATCTCA[C/T]TATGCCCTGGTAAAT	8925
rs558334372	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63752433	AAAATACGCATGTAA[A/G]AGTTCGAAGCTTATA	8925
rs558341750	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63670631	ATGGGAGCAAGGGGG[C/G]ATGATTCTACCACTG	8925
rs558342120	in-del	-/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63633010	GGGAGGGAGTGTGCA[-/G]GGGGCAGAGGCAGTT	8925
rs558387787	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63686654	CTACTATGAATCAGT[C/T]ACTGTGCAGGGCAAC	8925
rs558401501	snp	C/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63670688	TGAAAAGGTTACAAG[C/G]AGTCACAGTGCTACT	8925
rs558408622	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63618130	CTTCTAGGGTTTTTA[C/T]GGTTTTAGGTCTAAC	8925
rs558409738	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63622525	TTTAGTAGAGATGGG[A/G]TTTCACCATGTTGGC	8925
rs558423678	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63706159	ATTTGTACACACAAC[C/G]ATGAGTTAACTATAC	8925
rs558424855	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63663567	CTCAAGACATCCTCC[C/T]GTCTCAGCCTCTGAG	8925
rs558460419	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63755897	CTTGGCAATTACTTA[A/G]GTACTCTAAATGCCT	8925
rs558461638	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63662738	ATCAAATATTACCAC[A/G]GTATGACTCTATTCA	8925
rs558486038	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63699827	TCCAAGTCATTTGTC[A/G]ATATTAGCTTTAAAT	8925
rs558495535	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63702474	TGCTTAAGTTGCTGT[G/T]TTGATATCCCACAAC	8925
rs558507958	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63659172	ACAGGATTCTCTTAA[A/C]ACCAAGTTTTTTTTT	8925
rs558513090	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63640866	GTAACTATTTAACCA[C/T]AGAGATCTGCTCTTC	8925
rs558517787	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63764397	CTGCATCACATGATA[A/T]ATTAAGTGCCAATCC	8925
rs558520933	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63632635	GGACTCAATTTAGAG[C/T]ACATTCTGTAACACT	8925
rs558532800	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63731017	TTTAAAATATTTTTC[A/G]TAATATTGTACTGCA	8925
rs558537470	in-del	-/A	0.48978	0.0707512	intron-variant	HERC1	GRCh38.p7	15:63730027	GTGAAACTATGTCTC[-/A]AAAAAAAAAAAAAAA	8925
rs558543791	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63774228	ATATTTATTATCTGA[C/T]TCCTCTACTAGGCTG	8925
rs558559307	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63828636	GAGCCACCGCACCCA[C/G]CCCAGTACACCTTTT	8925
rs558570848	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63709002	TCAATCTGGTGTTTT[C/T]TGTTTGAGACAGTGT	8925
rs558586586	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63791101	TTTAATGGGTTTGTC[C/T]TTTCCTCGGACATAC	8925
rs558588443	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63710690	AAGAAGGAAAATTGA[C/T]ATTTTAAATAGGGTG	8925
rs558593540	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63639700	TTTCTAGAGTAGACA[C/T]TCTCAAATACAAACA	8925
rs558596547	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63788187	TTTGGGTTTCTATTC[C/T]ATAATCCAGTACAAG	8925
rs558628958	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63612633	CCTGTGGGGCTAGGC[A/G]CCTCCTGATGCCTGC	8925
rs558667337	snp	A/C	0.000399281	0.0141238	missense	HERC1	GRCh38.p7	15:63752978	CTGTTGATGTCAAAG[A/C]AAGTGAAGACTGGCT	8925
rs558679714	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63768138	TGCTCATCGTCTTCA[G/T]ATCTCTGATTCTATT	8925
rs558698448	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63750399	GAAAGGGTTAGGTGG[C/G]AAAAAAAAATTTTGT	8925
rs558700771	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63653555	TGTTGTCCTTCAGTA[C/T]CTGTGGGTGATTGGT	8925
rs558701964	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63773520	AGTGTTTGAGTCTTA[A/G]TATTTTAAATTTGTA	8925
rs558716578	snp	A/G	4.97376e-05	0.00498662	missense	HERC1	GRCh38.p7	15:63659768	TCTTCCATACTGTTG[A/G]TGGCTGTGACCATTG	8925
rs558727315	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63770600	TCATATAAGTTAATG[A/T]ATATATTGTGTGTTC	8925
rs558730237	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63646392	ACATAGACTTATCCA[C/T]GTATATCCATGGTCC	8925
rs558730583	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63639340	CAAATGCCTAGAGCA[C/T]TGAATACAGTCATAT	8925
rs558767777	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63814948	AGTTCATGAATAAAA[C/G]TGTATAACCTCAGAT	8925
rs558785385	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63801663	TAAGCAATCTGAATC[C/T]AGGTAGTCCATTATG	8925
rs558794620	snp	G/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63789252	CCCGCCACTACGCCC[G/T]GCTAATTTTTTGTAT	8925
rs558818464	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63666546	GTGTCTTCATAGTCC[C/T]CAATTTCCTAGTATT	8925
rs558834115	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63721211	GTCACCACAACAGAA[C/T]GAATGAATAAATGAT	8925
rs558840115	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63775841	CCAGGAGTTCAAGAC[A/G]AGCCTGGCCAACATT	8925
rs558846549	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63692994	AAGATCAGCCTGGCC[A/T]ACATAGCGAAACCCC	8925
rs558861254	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63673594	TTATTTCTGCATTCA[C/T]ATTCTCCCCAAATGT	8925
rs558862553	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63815962	TCTCATGAGAACTCA[C/T]TATCAGGAAAACAGC	8925
rs558880154	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835271	CACATATTAAGTACT[C/T]ATTAAATGATGGGTC	8925
rs558896629	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63739553	ATACAAATGGAGTTA[C/T]ACAGGCCGAGCGCGG	8925
rs558897895	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63672907	CCAGACTCTACAGAC[A/G]GTATTGTAATGAGCC	8925
rs558910066	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63690426	GTCCTAAAAGTAAAC[A/G]TTATGCTATTGAATA	8925
rs558948333	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63688179	TTGGAATAGGGTGAT[G/T]ACAGAAGAGATGAGG	8925
rs558949607	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63790109	TATAATGGATAATAA[A/G]AGAACCTCTATCATT	8925
rs558951219	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63782154	GGTAACTGATGAAAG[C/T]AGTTATATTAAACAA	8925
rs558955613	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63738423	AATAGTATTAAACCA[A/G]TACTAATTTATTTGT	8925
rs558964738	snp	C/G	5.0841e-05	0.00504162	intron-variant	HERC1	GRCh38.p7	15:63694564	TCTAAAAGACAAAGA[C/G]ACAGTTAAGAATCTT	8925
rs558970782	snp	C/T	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63653136	ACACAGACTAAGAAG[C/T]AATTTTAAAAATTGT	8925
rs558981306	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63642751	TGTCACCAAAGTATG[C/G]GGTGTAGTAGAAAAA	8925
rs558983623	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63649141	GGGCGGATCACAAGG[C/T]GAGGAGATCGAGACC	8925
rs558992615	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63828691	AGTGTTTAGTAACTA[C/T]AATGTTTCATATGCC	8925
rs559001694	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63783470	GACATAATGCTATTA[C/T]ACACTTAACAGACTA	8925
rs559024195	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63784921	TGGCCTATCAGTGCA[A/G]ATTTTCAAAAAGCAT	8925
rs559028866	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63829287	ATCAGCGGGGCATGG[C/T]GGGTGCACATCTGTA	8925
rs559029539	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63702844	GGCATGGTGGCTCAC[A/G]CCTGTAATCCCAGTA	8925
rs559039082	snp	A/C	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63645808	TTTATTTTGAAATCA[A/C]TATTTTATGCAAATC	8925
rs559039939	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63667404	CATGTGAAATAAACA[C/T]GGAAGATGAGATTAA	8925
rs559045360	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63684310	ACTAAATAAAACTGT[A/T]CCCAGAAAGAAACTG	8925
rs559063377	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63627073	GCTTCTGCCCTAAAG[G/T]GGAAGTGAAATCCCT	8925
rs559069035	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63795761	CATTTATAATCTCAC[A/G]CGTCCACCCTACTGC	8925
rs559075529	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63695829	CGTAAGCTCTTGAAA[A/C]CCATCCTCCCAAACT	8925
rs559136044	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63805181	GAAACTCGACTGTCC[A/C]TCATCTGATGAATGA	8925
rs559149479	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63791634	AAAAAACAATTCTTC[A/G]AGGGAGTTCAAATTG	8925
rs559156089	in-del	-/AAT	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63773985	AGGTTATGATAGTCA[-/AAT]AATTAATTTCCTCTG	8925
rs559167224	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63670276	CAGCCCCTTCTCCGA[C/T]GAGAATGTGGAGCAT	8925
rs559167441	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63814898	ATATGAAAGTATTTT[A/C]ATGCAATGTACTAAT	8925
rs559168430	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63725625	ATGCAAAATATTTTA[G/T]GATGAAAACACAAAT	8925
rs559179445	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63691003	CTCAGAGAAGTTATG[A/T]AACTTGACCAAAGCC	8925
rs559203741	snp	C/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63677249	AATTTGTAATTTGCA[C/G]AAATCCTCTCTGAAT	8925
rs559203799	snp	A/G	3.35632e-05	0.0040964	intron-variant	HERC1	GRCh38.p7	15:63669741	AAAAATCCAATTTAC[A/G]AAATAATACATACAT	8925
rs559220388	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63786646	TTGAAAGATGCCAGA[C/T]ATAAAAGGCTATATA	8925
rs559222352	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63757105	TTATGGCAAGAACCA[C/T]ATAAAATGTATTCTA	8925
rs559250292	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63732205	GGGGTTTCACCATAT[C/T]GGCCAGGCTGGTCTC	8925
rs559252868	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63712673	TTTTTGAAAAAATTT[G/T]TATATGTCTAAAACA	8925
rs559303381	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63817724	TGTCTCAAATAATAA[C/T]AACAACAACAATCCA	8925
rs559305327	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63813476	GATAGTGCGAAAGGG[-/T]TTTTTTTTAATATCA	8925
rs559305350	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63635479	TCAGCTGTGTACACA[A/T]GACCTAGACTAAATG	8925
rs559312276	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63688811	TTATGATAATCTAGC[A/G]TTCCCAGGAATTTGC	8925
rs559331057	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63822523	CTCAGGAGGCAGAGG[C/T]TGCAGTGAGCCGAGA	8925
rs559356812	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63824260	TAAAAAGGGCTGGGC[A/G]CAGTTGCTCACGCCT	8925
rs559372073	snp	A/C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63805748	GGTCAGCAGTTCAAG[A/C/T]CCACCCTGGGCAATA	8925
rs559376721	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63727045	CATTTTGGGAGGCTG[A/C]GGTGGGCGGATCACA	8925
rs559383475	snp	A/T			upstream-variant-2KB	HERC1	GRCh38.p7	15:63835911	CCCTCTTTTACCATC[A/T]CCTTAGCTTCCACCC	8925
rs559384281	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63799239	GGCACAGTGGCTCAC[A/G]TCTGTAATCACAGCA	8925
rs559387634	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63680302	TTAACCTTGCTAACC[A/G]AGAAAATTCTACATA	8925
rs559414819	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63699027	ATAAACATATATCAA[C/T]GGCAATCAAGTAGAG	8925
rs559427570	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63818356	AGTTTTATCTTGTGT[A/G]CAAAAACCCTTTCCT	8925
rs559430655	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63690068	ACTTGGAGGCTAAGG[C/T]AGGAGAATCACTTGA	8925
rs559483174	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63830098	TCTACCAATGGATGT[C/T]AAAAATCAATGGGAG	8925
rs559493627	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63610034	GACAGGATTATATAC[A/G]TTCCCTATCCCTCCT	8925
rs559508588	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63729789	GCACTTTGGGAGTCC[A/G]AGGCAGGTACATCAC	8925
rs559515076	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63793386	ATTATACACTAATTA[G/T]AATGCATTAGTATGC	8925
rs559519923	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63830516	GGAACCTAGATTAGA[A/C]CCTAGAACAAAAAAA	8925
rs559520985	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63820063	TTTAGTCATTCCACA[A/G]TGTATATATACTTCA	8925
rs559543823	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63615335	AAGGAATCACCAAGT[A/G]CGGTGGCTCACACCT	8925
rs559545363	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63728873	AGAAGCCCAAAGAAA[G/T]AATTTCAAGAAGGAA	8925
rs559567334	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63656511	TAAGAGTTGCCAAAG[A/G]TATCAAGCTGGAAAC	8925
rs559571278	snp	C/G/T	0.000422303	0.0145252	intron-variant, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609316	ATCAGAGTGCCATAA[C/G/T]GGGGAGTGGGGCTGC	8925
rs559574246	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63664378	GGGACTGAGCACTTA[A/G]TATCATTAGTTTGAA	8925
rs559618397	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63763710	GAGAAAAGAGGTTAT[A/G]ACAAGGCTGTGAAAG	8925
rs559623183	snp	A/G	0.00874735	0.0655527	intron-variant	HERC1	GRCh38.p7	15:63706287	CATGTAAGAGATAAA[A/G]CATCTCTTACATGCT	8925
rs559650947	snp	A/T	1.68306e-05	0.00290087	stop-gained	HERC1	GRCh38.p7	15:63692518	CTGCGAAGAAAAACT[A/T]AAAAATCCCCTAGAT	8925
rs559683447	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63630310	TCGAGAGAGAAAGAC[A/C]TAACTAGACTTACAA	8925
rs559697735	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63792995	AAACACTTATACTTA[C/T]ATTTATGGGTTTATA	8925
rs559707822	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63802295	AAGAAAAAACTTTTT[C/T]GTTGTTATTATTGCT	8925
rs559722052	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63702569	GTCTTTCTGTAAACA[A/G]TCGTACAACCATAGC	8925
rs559727595	snp	A/G			synonymous-codon	HERC1	GRCh38.p7	15:63678249	GTCTGTTCGGTGAAG[A/G]ATACGGATGAGCTGA	8925
rs559730426	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63719649	AGTGAGAAATGATGA[C/T]GACTCAGAAAAAGGT	8925
rs559731394	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63748579	TAATACTTTTCAGTT[C/T]TTGGGACCCAACTAT	8925
rs559732633	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63727542	TGATGAAATTCCTTT[C/G]ATAGCCTTAGGATAG	8925
rs559780899	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63644190	TCTTCCTTTTAGTTA[C/T]GACAACATAATACTA	8925
rs559807852	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63801336	CTGGCATCTGAAGTA[C/T]GAGTAGTCTTGTGGG	8925
rs559846653	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63792001	GGGGGCAAAGTGTAA[A/T]AATTGATAACTGATT	8925
rs559861407	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63819317	ATTTGTCAAATGGAA[A/G]AATAACATCTGCCTG	8925
rs559863025	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63612814	TAGGAGCCTGCCTTC[C/T]CTCTACCACAAAATC	8925
rs559864310	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63616233	AGGGGGAAGGAGCAA[C/G]TAAGTGCAGGAGCCT	8925
rs559871336	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63752699	GTTTAAGGGAAGCTA[A/C]ATGCTAAAACATTTT	8925
rs559880838	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63617385	GGTGTATAAGTGCCA[A/C]ATTTTCTTAATCCAG	8925
rs559889672	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63638945	ACTTGATTTTATGCA[C/G]TGTCAGTATTTCCCT	8925
rs559898999	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63709650	TTTCCCAAAAGTACA[A/C]CACTTTAATTTTACC	8925
rs559915714	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63747979	GCCTGTAATCCTAGC[A/G]CTTTGGGAGGCCAAG	8925
rs559925796	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63660085	ACACTCTGGGAGGCC[A/G]AGGCGACTGGATCAC	8925
rs559929561	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63745011	CTTCAAGGCAGTGGG[C/T]TCCCTTCTGGCCTGG	8925
rs560006246	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835011	GAGGGAGTGCTTTCC[C/T]ATGGTTAAATTAGAT	8925
rs560024348	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63780547	TAACACGGTGAAACC[C/T]CATTTCTACTAAAAA	8925
rs560028255	snp	A/T	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63780074	CCCTTCCAACACACT[A/T]TTGAGGTTCCAATCT	8925
rs560043979	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63828463	TCCTGCCTCAGACTC[C/T]TGGGTAGCTGGGATT	8925
rs560044225	snp	G/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63696011	GCTATCTTAAAAAAT[G/T]TAAAGTCTTTGTATT	8925
rs560044281	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835417	ATTGTGTGTGAAGCA[C/T]ACTCAAAAACAACAA	8925
rs560053607	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63822220	AGGAGAGGGAGGCAG[A/G]GACTACATCATGTAG	8925
rs560071266	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63641790	GCTATGCTTTTAATG[A/C]CTATGGAACTTCAAA	8925
rs560073070	snp	G/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63620040	CCTTCTGCTAGCTTT[G/T]GAATGTGTTTGCTCT	8925
rs560091433	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63779486	ACATAAATAGAAACA[C/T]TAATAACGTGAGACA	8925
rs560093522	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63745471	TCTGGCTAGGGTTGG[C/T]TTAAATGCTCCCTCT	8925
rs560112800	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63739644	AGGAGTTCAAGACCA[A/G]CCTGGCCAACATGGT	8925
rs560147059	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63614117	CCAAAGACCAATTCA[C/T]ATATAAAGAAAGAGG	8925
rs560152325	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63759573	GTTAGCAAAACTAAA[A/G]TTTTTCCATCTATTT	8925
rs560153654	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63752659	AGTTCAGCTTTCCCC[A/G]ACTATCCATAATGTT	8925
rs560163837	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63659218	TAAATCTTTTTATTG[C/T]TTCGGTATCATGAAA	8925
rs560166337	snp	A/T	2.27949e-05	0.00337593	intron-variant	HERC1	GRCh38.p7	15:63725255	AACTGAGGTACAAAC[A/T]GGCATGTATTTTAAA	8925
rs560176021	snp	A/T	6.89774e-05	0.0058723	intron-variant	HERC1	GRCh38.p7	15:63612239	CAAAGGAAAAAAGAA[A/T]AGCTTACTTACCCTA	8925
rs560185131	snp	A/C	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63646886	GTAAAGATGCTTTTA[A/C]CAGAATATATACAAA	8925
rs560187222	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63653312	GCCGAGTGTGGTGGT[A/G]TACATCTGTAATCCC	8925
rs560206190	snp	C/T	0.00755907	0.0610114	intron-variant	HERC1	GRCh38.p7	15:63827675	AAAAATATATGTCCA[C/T]ACAAAAAATTGTACA	8925
rs560234541	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63803791	AAGGCAGGAAGGCAA[A/T]GGACTGAGAATAGCA	8925
rs560240232	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63769105	TTCAGTCAGTTACGA[C/T]TGAAGACACACCTAA	8925
rs560240690	snp	A/G	0.0263992	0.111815	intron-variant	HERC1	GRCh38.p7	15:63618321	TAGTTGTAGATATGC[A/G]GCATTATTTCTGAGG	8925
rs560272918	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63816809	AAATGCCATCTAACA[C/T]ATGAATGAAGAAGGA	8925
rs560278331	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63766726	CTTGTTGCCCAGGCT[A/G]GAGTGCAATGGCACG	8925
rs560291838	snp	A/G			downstream-variant-500B, utr-variant-3-prime	HERC1, FBXL22	GRCh38.p7	15:63608349	AGGGGCGGAGCAGCT[A/G]AGGGAACAAAGTCAG	8925
rs560309978	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63648788	TCACTGTATGCTTTT[A/T]AAAACTTGAATTTTT	8925
rs560312056	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63747224	CAGCACTTTGGGAGG[C/T]GGAGGTGGGTGGATC	8925
rs560314975	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63761222	GAATAGACACTGACA[A/C]AGAGACTAGTATTGA	8925
rs560315151	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63751998	CATGATGCTCAAGGG[G/T]TGTCTGTTATTTGCC	8925
rs560341489	in-del	-/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63613066	AAAATCTGAAAAGTA[-/C]AAAGAAGAAAGTAAA	8925
rs560347756	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63682260	TCACAAGAGAGTTGG[C/T]TTGCTACCCCAGACG	8925
rs560356918	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63739300	TCTCAAAGGTTCAGG[C/T]GATTCTCCTGCCTCA	8925
rs560370695	snp	A/T	0.0103295	0.0711199	intron-variant	HERC1	GRCh38.p7	15:63790586	CCGTCTCAAAAAAAA[A/T]TTTTTTTTTTAAAAA	8925
rs560384093	snp	G/T	3.31285e-05	0.00406978	missense	HERC1	GRCh38.p7	15:63654156	TTGATAAAGGAGCAT[G/T]TTCTAAGATCTCCTC	8925
rs560384344	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63658226	CTTAGCTACACAGAC[A/G]GTCAATACATTTTGA	8925
rs560404302	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63753459	AACTTTAAAAAAGAA[C/T]GTATATGCATATAAT	8925
rs560413423	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63634102	ACAATGGTTTCAGAG[C/T]ATACTACAAATGTTA	8925
rs560423588	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63768235	TAATTATTTAGGATG[C/T]TGCTTCTCAAATTTC	8925
rs560427302	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63783108	ACATAAATTTAATTG[A/G]TAATGCAGTAGCAGA	8925
rs560465696	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63782615	ATTCTGCAGCACATG[C/G]ATAAAGAAGTCATTT	8925
rs560487115	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63809666	TGAATTTTAAGGACA[C/T]TTAGAAGGTATACTC	8925
rs560488483	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63690031	TAGCCAGGCATGGTA[G/T]CATGTGCCTATAGTC	8925
rs560493630	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63803382	AACCACTAAATCATG[C/G]TGCTTCTTATCAACA	8925
rs560496195	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63620906	GCATGTGAGATGGGT[C/T]TCCTGAATGCAGCAC	8925
rs560500914	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63764914	AATGGAGGAGTTTAA[C/T]TGGTATATGACCTTC	8925
rs560505113	snp	A/G/T	0.000183373	0.00957386	synonymous-codon	HERC1	GRCh38.p7	15:63622841	GTAACCCACTTCTGC[A/G/T]GTGGCATTGGGAGAG	8925
rs560520631	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63667690	ATATGAAGTGGTACA[A/G]TATCACCTTAAGGTA	8925
rs560541295	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63693092	CTGAGGCAGCACAAT[C/T]GCTTGAACCTGGGAG	8925
rs560549099	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63798354	TTTTAACCAACAACT[A/G]CCTCTTTACAATCAG	8925
rs560550739	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63717751	GTGGTGCATGCCTGT[A/C]ATCCCAGCTACTCGG	8925
rs560551366	in-del	-/ATAT	0.030665	0.119967	intron-variant	HERC1	GRCh38.p7	15:63737455	ATATCTTTTTTCCAG[-/ATAT]ATATATATATATCTT	8925
rs560575175	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63744902	GGCTCACCCAAAGCC[C/T]TTGACATAGCAGCTG	8925
rs560583578	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63777893	TAAATTCTACATTCA[C/T]CTGGAAGTTTAATAC	8925
rs560588491	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63673976	GTGATCTGCCCACCT[C/T]GGCCTCCCAAAGTGC	8925
rs560599677	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63728799	AAGAGGAGCCTATAG[A/G]AACCCACTGAAAAAG	8925
rs560607131	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63614443	CTCTGAGGATTAAAA[A/C]TATTCATCAACTGGA	8925
rs560613374	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63762952	TCAAGTAGCAGAACA[C/T]GTTCCATATAAATGC	8925
rs560635487	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63755695	TGAGTTGGGAGGACC[A/G]CCTGAGCCCCAGGAA	8925
rs560636144	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63697747	GGAGTGAGCCACCGC[A/G]CCCGGCCAATCTTAA	8925
rs560649163	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63768330	AAGCCTAAGATTCTG[C/T]ATTTCTAACAAATGT	8925
rs560677788	in-del	-/ATCTTTTATGGCAG	0.0170251	0.090679	intron-variant	HERC1	GRCh38.p7	15:63657650	TATTCCAATTTATCA[-/ATCTTTTATGGCAG]ATTCCTTTTGTGACT	8925
rs560684115	snp	A/G	0.0333695	0.124785	intron-variant	HERC1	GRCh38.p7	15:63816093	GGACACAGCCAAACC[A/G]TATACCTAACATTTC	8925
rs560685088	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63717068	TACTCAGACAGTCAT[A/G]AATACCATTCAGTAT	8925
rs560705099	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63671937	TCATTTGTATATACA[C/T]CTGGCAAATTAAAGC	8925
rs560729417	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63803850	TAAAGATGTACATTA[C/T]CTGACTTTTAAGCTT	8925
rs560734300	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63721202	CTGGTAGGAGTCACC[A/T]CAACAGAATGAATGA	8925
rs560744706	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63651427	ATCCCCATCATTCAA[A/G]AGTAAATTAAATCCC	8925
rs560772497	in-del	-/TTC	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63700924	TAAAAAATATATACA[-/TTC]TTTTTTCATTTCCTT	8925
rs560780538	in-del	-/AT	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63647516	TCTACCCAAAGGAAA[-/AT]ATAATTCATTTTCTC	8925
rs560782886	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63657682	CCTTTTGTGACTTGC[C/T]TGAGGAATTTTTGCT	8925
rs560789756	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63615472	AAGATTAGCTAGGCG[C/T]GGTGACACATGCCTG	8925
rs560799789	in-del	-/AA	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63774539	ATTATCAACATGCAT[-/AA]AAGTTTCTTCACTCC	8925
rs560807995	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63767576	GGTGGCGGGCACCTG[C/T]AGTCCCAGCCACTGG	8925
rs560808775	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63703714	ACATGGCGAAACCCC[A/G]TTTCTACAAAATAAA	8925
rs560819606	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63657169	ATGGGAGTTTTAGCT[A/G]TTTCAGTCACTTTTT	8925
rs560830922	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63833308	AGGCAGAGGAGAGGA[A/G]GAAGACACGTCGTCC	8925
rs560831799	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63688373	AGGGTGCCATTTTTG[A/G]CATACTGAGTATGAG	8925
rs560833811	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63771977	CAGAAACAAAATTAG[C/G]TGGGCATGGTGGCAG	8925
rs560839149	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63765482	ATTATATCCATCCAG[C/T]GTTAACATCAATACT	8925
rs560868625	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63819256	CTAGAGGTTGAGATT[A/T]TTCAGGGGCTCATTC	8925
rs560874237	snp	C/T	4.97187e-05	0.00498567	missense	HERC1	GRCh38.p7	15:63758206	AAACTAGGAGCCAGT[C/T]TGGGTTGCAGTATTT	8925
rs560878039	in-del	-/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63811422	AAGCGCTATTCTTCA[-/T]TTTTTTCTATAAATC	8925
rs560882720	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63750070	TGCTAAACCACTAAT[A/C]GGCTTGCAATTTGTT	8925
rs560887886	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63613621	ATCTATATGCATATC[C/T]TATATTATCGTGTTG	8925
rs560889527	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63805942	AGCAAGACCCTATCT[C/T]AAAACAAAAAAAAAA	8925
rs560914464	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63721985	TGTCCTTTAGCCTCC[A/C]GAGTAGCTGGGATTA	8925
rs561000736	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63804053	GATAATCTTTTCAAC[A/G]AAAGGTGCTGGACCA	8925
rs561001358	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63651893	ATACAAAAATTAGCC[A/G]GGCATGGTGGCAGGC	8925
rs561015434	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63787268	TTCAAGCAATTCTCC[C/T]GCCTCAGCCTCCCGA	8925
rs561031797	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63700412	TGGGAAGATAACTAC[C/T]TAAACACTAATGCCC	8925
rs561049495	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63660602	TCTGTAATCATTAGG[A/G]AATGAGTTATTTCAA	8925
rs561071917	snp	C/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63638048	CGCTATATCGTACCA[C/G]GATTATTAGAAAAGG	8925
rs561111332	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63610433	GACAACCCTGAGACC[A/G]GAGATTAGTGGTGGA	8925
rs561181281	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63635142	AGCCCCAAACTCCTG[C/G]GCTCAAGCAATCCTC	8925
rs561196356	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63673256	CCTACAAATAAACAT[A/G]ACTAAAATATGAGTT	8925
rs561206107	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63824270	TGGGCGCAGTTGCTC[A/C]CGCCTATAATCCCAG	8925
rs561208658	snp	C/T	1.67301e-05	0.00289219	missense	HERC1	GRCh38.p7	15:63664554	TAGCTGATGGTCCAC[C/T]TCCAGAAGCTGCATT	8925
rs561227429	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63781183	TATAAAACAATGAAG[C/T]GGAAACCACAGAGAA	8925
rs561227500	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63779076	GAAGAGTAGACTCAA[A/T]GACATAAAGAAAAAT	8925
rs561231661	snp	A/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63681209	TTTTGTTTTGTTTTT[A/T]ATTTTCTAAAGAGAT	8925
rs561233843	snp	C/T	7.87216e-05	0.00627332	synonymous-codon	HERC1	GRCh38.p7	15:63672522	AAGAGGCATCACTCC[C/T]GGGGACTCGGATGCA	8925
rs561236062	snp	G/T			missense	HERC1	GRCh38.p7	15:63775065	CATCGTTGCAAAGAC[G/T]GAGACCAGGTCCTGA	8925
rs561247392	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63671727	AATTGAGAATCACTA[A/C]AATAGACACTCCCCT	8925
rs561262339	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63801624	CACATAGAGGGAGCT[A/C]AATAAATATTTCCTG	8925
rs561283677	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63617648	AAAGTGTTCCTATTT[A/C]TCCACATTCTCTCCA	8925
rs561302881	in-del	-/C	0.00676609	0.0577691	intron-variant	HERC1	GRCh38.p7	15:63743271	CTTTTTCTTTTTTTT[-/C]TTTTTTTTTTAAATG	8925
rs561312280	snp	A/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63684659	TCGGGAGGGCATTAA[A/T]GATCTGTTTTTCAGA	8925
rs561330374	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63736866	CCCACCTCAGCCTCC[C/T]AAAGTGCTGGGATTA	8925
rs561333214	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63641067	ACAAAGATTTATCTA[A/G]TAAGTGGAGACGATA	8925
rs561339656	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63715928	CTCTCCTAATAGGCA[A/T]AGAAAGGGGCTCTCT	8925
rs561363746	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63650178	GAGGCCAAGACGGGC[A/G]GATCACCTGAGGTCA	8925
rs561364550	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63832696	GCCCAGTGAAAAAGA[C/T]AGTGATGGCAGAGTT	8925
rs561370213	snp	A/C	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63800932	GTTCCACCACCAGAC[A/C]TCAAGGGAGAGGAAA	8925
rs561374556	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63722985	ACAGTAGGTTTAAGT[A/G]GAATACATGTATATA	8925
rs561388003	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63784051	AGCCTGGTGACACAG[A/G]AAGACTCTATCTCAA	8925
rs561395975	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63744004	GTTGTGGTTCTTGCA[A/G]CCTCATAGAGGTACC	8925
rs561401610	snp	G/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63833654	GGGCTCCCCCAGCTC[G/T]CCTGCCGCCCACCCG	8925
rs561402290	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63654772	TACTCGGGAGGCTGA[A/G]GCAGGAGAATTGCTT	8925
rs561406416	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63613304	CTCTGTTCTCTTAGC[A/C]TCATAGTGCTGGGCA	8925
rs561452409	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63790967	TTTATAGAAGGCTTG[C/T]TTTTACGAACATCAT	8925
rs561475390	in-del	-/G			intron-variant	HERC1	GRCh38.p7	15:63707954	AAAAAAAAAAAAAAA[-/G]AAGAAGTGACAAAAC	8925
rs561482820	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63766970	GGCGTGAGCCACCAT[A/G]CCCAGCCTACACTAA	8925
rs561485833	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63624711	ATATTATTTGAAAAA[C/T]TGAAAAAAGAACATA	8925
rs561489145	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63689931	CACTTTGGGAGGCTG[A/G]GGCGGGTGGATTGCC	8925
rs561506437	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63642728	GAAATTGTTCAATAT[A/C]TAAGCACTGTCACCA	8925
rs561514800	in-del	-/C			intron-variant	HERC1	GRCh38.p7	15:63670684	GAGCTGAAAAGGTTA[-/C]AAGGAGTCACAGTGC	8925
rs561518069	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63731205	CAACTTTTTTTCCTG[C/T]AAATAATCATGTGCT	8925
rs561519585	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63814764	GTGAGCCACCACACA[C/T]GGCCAACATTAGCTT	8925
rs561541518	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63830398	AAGAAGTTCTAAAAA[A/T]TAACAGTACTCATCA	8925
rs561547451	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63648668	CTATATTTCTACTTG[C/T]TTCTTCAAGTATATG	8925
rs561565702	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63811004	ACTGGCCTAGATTAT[G/T]CAATAAAGTTAATGT	8925
rs561589959	in-del	-/ATAT	0.0295035	0.117819	intron-variant	HERC1	GRCh38.p7	15:63737428	ATATCTTTTTTCCAG[-/ATAT]ATATATATATATCTT	8925
rs561596083	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63797591	CCACCCATCAAACTA[C/T]CCTTGAAAACCCTAA	8925
rs561616574	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63697682	CTGGTTTCAAACTCC[C/T]GATCTCAGGTGATCC	8925
rs561626603	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63754367	GTTAAAGTAACATTT[C/G]TAAAAGCTCAGTTCA	8925
rs561639734	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63774415	ATTTTTCATAAGTTC[A/G]CTAAAACATAAAGTT	8925
rs561673146	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63821530	CACTGCACTCCAGCC[C/T]GGTAACAGAGTGAGA	8925
rs561686804	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63788448	TCTATCATGACTTCA[A/G]CAGACAATTCCTAAG	8925
rs561693327	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63740516	GCCTGTTTTCCAAAG[C/T]ACCTGCACCATTTTA	8925
rs561693782	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63829870	CTGGAACAATTTGAA[C/T]AACAAAATAAATAAT	8925
rs561712552	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63706273	ATATAATATCTCTTC[A/C]TGTAAGAGATAAAGC	8925
rs561716616	snp	C/T	0.00279162	0.0372561	utr-variant-3-prime	HERC1, FBXL22	GRCh38.p7	15:63608877	TGACTGAGAGCACTT[C/T]GTTTTTGTTGTTTTT	8925
rs561736509	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63823412	CCTATGACGTAGCAA[C/T]TATAATTATTCCCAT	8925
rs561752364	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63726902	TATAGAAAAATATCA[A/G]TTATAAACATAGATG	8925
rs561775702	snp	C/T	0.000146784	0.00856564	synonymous-codon	HERC1	GRCh38.p7	15:63648159	ATATCCCACTGCAAA[C/T]GGTCTGTCTTCACTG	8925
rs561781178	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63769997	ATTAGACGGAGTACA[C/T]TTCCTTCCGTTCTGG	8925
rs561804751	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63811623	GACCATCCTGGCTAA[C/G]ATGGTGAAACCCCGT	8925
rs561820476	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63689147	GATCCGGGAGAAAGC[A/G]TTTTGAAAATAACAA	8925
rs561824317	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63746104	TCTTTTTCTAATTTC[C/T]TAAGGTAGAAGGTTA	8925
rs561826875	snp	C/T	3.31559e-05	0.00407147	missense	HERC1	GRCh38.p7	15:63628740	AGCGGCCAGCCGAGA[C/T]CTGCCGAACATTTTT	8925
rs561844357	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63777328	AAGAGGGGGGAAAAT[A/C]ATGATCCTCCATCCC	8925
rs561874369	snp	A/G	0.00874735	0.0655527	intron-variant	HERC1	GRCh38.p7	15:63741274	CCTCGTGATCCACCC[A/G]CCTCAGCCTCTCAAA	8925
rs561878155	snp	C/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63824113	TGACACCTGTGAGGA[C/T]GGCAATTATCAAAGA	8925
rs561882833	snp	C/T	0.0287284	0.116357	intron-variant	HERC1	GRCh38.p7	15:63621241	AGTATTTTATTTCTC[C/T]TTCACTTATGAAGCT	8925
rs561885448	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63711999	GCTTTATATTTTACC[A/G]GTGACACTGTAGCAT	8925
rs561887691	snp	G/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63636274	GAATAATTTCATTAG[G/T]TTTTTTTTTTTTTTT	8925
rs561918753	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63733806	ACAGTAAGCCATGAT[C/T]GTGCCACTGCACTCC	8925
rs561933938	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63727917	TAATAAATATTATTT[C/T]AGCTTGGAACTAGAG	8925
rs561953133	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63778413	TTAAAGCAGAAGGCA[C/T]GGTTTAAGACAGCAG	8925
rs561958880	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63668738	AACGTAAGAATCCTA[A/G]ATGTTTATGAACCTA	8925
rs561968985	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63726203	GCCAGGCTGGTCTTG[A/G]ACTCCTGACCTCAGG	8925
rs561996797	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63635209	TGTGCTACCACACCT[C/G]GCTATTTATTTCTAT	8925
rs562007788	snp	C/T	3.31214e-05	0.00406935	missense	HERC1	GRCh38.p7	15:63661963	TTGAAGCTGACGACG[C/T]TGCATTCACACAGTT	8925
rs562025184	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63756107	AAAGTAGAGACCTTA[C/T]CTGTCTTGTTCACTG	8925
rs562027089	in-del	-/AATT	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63796190	TTTACAAGTAGAATA[-/AATT]AATTATATTTTTTAA	8925
rs562051534	snp	C/T	0.000302644	0.0122976	intron-variant, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609288	AGAGAGACCCAGAGC[C/T]GTGACTGGGGACATC	8925
rs562054951	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63656442	CACATAACATTCACA[C/G]CATCAACAACCATAA	8925
rs562057958	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63715226	AATGAGCTAATCTAT[C/G]CAAAGAACTTGACCA	8925
rs562060316	in-del	-/TACAG	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63751218	TGCCAGTATTTTTAC[-/TACAG]TGTAACTTTTCTATG	8925
rs562066624	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63780717	ACACAATGAGACTCC[A/G]TTTCAAAAAAAAAAA	8925
rs562077853	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63831114	TGTTTGTTTTGTTTT[A/G]TTTTGCTTTTGAGAT	8925
rs562088571	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63615678	TTAACACAGTAAATA[C/T]ATATTAGCAGATTTT	8925
rs562089946	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63621752	ATTTGATCTTCCATC[A/G]CTGATACCCTTTCTT	8925
rs562093535	snp	C/T	2.01201e-05	0.0031717	synonymous-codon	HERC1	GRCh38.p7	15:63655938	TAGATTTACACCTGT[C/T]GCAGCAGAAATCAAG	8925
rs562111689	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63792640	TGGATGATATAGAAC[A/G]AAAGAACTCAGTTTC	8925
rs562116882	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63709158	CACCCAGCTAATATA[C/T]ATATATATTTTTTAT	8925
rs562141568	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63662893	GACTTTTTAGAGTGT[C/T]TCAACTCTAGGCAAG	8925
rs562145974	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63708501	AAATCCTGCCAGAAA[C/T]GAGGGAGCTAGGGAA	8925
rs562161358	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63643994	CTGTCTGTCACACAT[G/T]TGTTCTGCAAGCTTT	8925
rs562170183	snp	A/G	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63804455	GCCGGGCATGGTGGC[A/G]GGCGCCTGTCATTCC	8925
rs562189176	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63755576	TTGAGCTCAGGAGTT[A/C]GAGTTCAGCCTGGGC	8925
rs562208207	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63741679	TTTTTTGTATATGAT[A/G]TAAGGGGCCAACTTC	8925
rs562224109	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63684961	TTGCAGTGAGCCAAG[A/G]TCGCACCACTGCACT	8925
rs562242199	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63691617	TATCCTCTTGAAACT[A/T]AATATAAGCCTTACC	8925
rs562242252	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63747914	TGAAATTTTTATGCA[C/T]GATCAAAAACGAAAA	8925
rs562245954	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63641734	AATTCCTTCTAGTAA[C/G]TGGGACATCTTTGCT	8925
rs562266255	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63818846	CCACCTCTATGCTAA[A/T]CCATGATACAGTCAA	8925
rs562271038	snp	C/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63692313	GAAAAGCCTTCAAAT[C/G]AAGGTTACACATGGA	8925
rs562272047	snp	C/T	1.65858e-05	0.00287969	missense	HERC1	GRCh38.p7	15:63698942	AACCAGTCTCTGCTA[C/T]GTTTCAGGCGAGCCC	8925
rs562282768	snp	A/G	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63825033	ATGAGGGCTGGGCAC[A/G]GTGGCTAATGCCTGT	8925
rs562283218	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63715739	ACTTCTCTTTAAACA[C/T]ATAAATAACTACCTT	8925
rs562285347	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63814720	GTTATCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC	8925
rs562286044	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63680480	GGCACTTGAATAACC[A/G]AGTTGACTATAAATA	8925
rs562287214	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63644690	ATGGATGTGCTCCCA[C/T]GGAGTTTCTATTTTA	8925
rs562296903	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63618278	ATCCTTTCCCCATTT[A/G]TTTCTGTCAGGTTTG	8925
rs562308509	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63701567	TAAATAAATGAGTGT[A/G]GCTGTGTTCCAATAA	8925
rs562309118	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63786544	ACAAAATGTCATATT[A/G]TCTACACAGTGGAAT	8925
rs562372272	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63738609	GAAAATGGTGGGAAA[C/G]CATACAAGAAACAGC	8925
rs562373857	snp	C/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63785875	AGAGAGATTATTCTT[C/T]TTTTTCTTTTTTAGA	8925
rs562393237	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63823298	GGCTTAGGCTGAAGA[C/T]ATAAATGTGAGTCAA	8925
rs562400655	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63807058	GCCTGAGTGATTTTT[C/T]TAAGGCTCAAAATCC	8925
rs562465061	in-del	-/AAAA	0.00518545	0.0506541	intron-variant	HERC1	GRCh38.p7	15:63738553	ACAGGTAGTTCAAAT[-/AAAA]AAATTTTTTAAAGAA	8925
rs562467711	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63759493	TATCATGCTTTTAAA[A/T]TTTTTGGCAAACATA	8925
rs562482745	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63612135	GGAGGTTGCAGTAAG[A/C]TAAAATCATGCCACT	8925
rs562515772	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63703576	CCTCCTCAAAATATT[A/G]GAAGGGGTAAACAAG	8925
rs562520748	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63647323	CACCCCAGTCAGGAT[A/G]GTTATTATTAAAAAG	8925
rs562536257	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63731350	AACAAATTTGGTTTA[A/T]ATCACATCAGAAAGA	8925
rs562556788	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63766544	AGATCGCACCACTGC[A/G]CTCCAGCCTAGGTGA	8925
rs562566303	snp	G/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63633292	ATAAGCTGAAGCTTT[G/T]TAAATCACACTGCTT	8925
rs562590891	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63767653	CAGTCAGCCGAGATC[A/G]CCCCACCGCACTCCA	8925
rs562591829	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63766957	TGCTGGGATTACAGG[C/T]GTGAGCCACCATGCC	8925
rs562624020	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63687469	CTTGAACCGGGGAGG[C/G]AGAGGTTGCAGTAAG	8925
rs562638748	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63712529	TAACCCAACTCATTC[A/G]GGTGGAATGTCCATC	8925
rs562651353	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63624600	CTCAGGAGGCTGAGG[C/T]GGGTGGATCACCTGA	8925
rs562701987	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63710669	ACAGGAAGTGACTAT[C/T]TGGAAAAGAAGGAAA	8925
rs562701998	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63741085	CCAGGCTGGAGTGCA[A/G]TGGTGCGGTCTCCAC	8925
rs562706240	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63789381	AGGCGTGAGCCACCG[C/T]GCCCGGCCAAAAGGT	8925
rs562710652	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63828417	TGATCTTGGCATACC[A/G]CAACCTCCGCCTCCC	8925
rs562716957	snp	A/C	0.0209421	0.100162	intron-variant	HERC1	GRCh38.p7	15:63646833	AAACAAACAAACAAA[A/C]ACAAAAACAAAACAA	8925
rs562719614	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63725143	TTAACCATTTTTCTT[A/G]GGGCTCCAAGTCATA	8925
rs562735756	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63653994	TAATTGTGTGCATGT[A/G]TATGTGTACGTGTGA	8925
rs562753129	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63652717	GAGTGCAGTGGCTCA[A/G]TCTCAGCTCACTGCA	8925
rs562771427	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63660661	CTCATCTCTATTTAT[C/T]TTTTACTTTCCACAA	8925
rs562782370	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63797599	CAAACTATCCTTGAA[A/G]ACCCTAAACTCCAAG	8925
rs562797682	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63751752	ATATATTTGATTTCA[C/T]ATAACTTAAGGTACT	8925
rs562808738	snp	A/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63660112	TCACATGAGGTCAGG[A/T]ATTTGAGACCAGCCT	8925
rs562829235	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63768183	ATTGCTGGGTCATCT[G/T]CTATTAACCTGCTGC	8925
rs562860818	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63626609	ACTAGGGATCTGATA[A/G]CAAGTATTCATGACA	8925
rs562864496	snp	A/G	0.0107246	0.0724382	intron-variant	HERC1	GRCh38.p7	15:63762417	TAACCTCCACCTCCC[A/G]GGTTCAAGCAATTCT	8925
rs562865023	in-del	-/T	0.00398802	0.0444759	intron-variant	HERC1	GRCh38.p7	15:63795537	CTCTGATACAAAAGG[-/T]TCCTATTTTGAATTA	8925
rs562883741	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63818624	TATTGGATTTTATTC[C/T]TTTATATGGCGTAGC	8925
rs562889800	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63816017	CATTTACCTCCCACC[A/G]GGTCCCTCCCCCCAC	8925
rs562891762	snp	A/G	0	0	intron-variant	HERC1	GRCh38.p7	15:63808805	TTCTAGAGGAATGAA[A/G]ATCCTGAGGGTCCTT	8925
rs562895279	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63823524	TGGGGGAAAGAACAG[A/C]TCTAACTGGTGACAA	8925
rs562911062	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63722080	ATGTTGGCCAGGCTG[G/T]TCTCAAACTCCTGAC	8925
rs562915020	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63691217	ATGCCTGTAATCCCA[A/G]CACTTTGGGAGGCTG	8925
rs562918238	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63724557	TCTCAGTCTCTCTTA[C/G]ACTTTCCTTCAGGGA	8925
rs562940659	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63673952	CTGGTCTAGAACTCC[C/T]GGCCTCAAGTGATCT	8925
rs562954472	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63645726	CAGAGTAATGTTTCC[G/T]TCACAAATACTTTAA	8925
rs562970831	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63803770	TTCACAGTCTCAGAA[A/G]CTTGCAAGGCAGGAA	8925
rs562982275	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63722146	GCTGAGATTACAGGC[A/G]TGAGCCACTGTGCCC	8925
rs562988556	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63771053	AATTAGCCAGGCATG[A/G]TAGCAAGTGCCTGTA	8925
rs562989999	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63773356	GGCTGAGGCAGGAGA[A/C]TCGCTTGAACCCAGG	8925
rs563011351	snp	C/G	6.63482e-05	0.00575931	missense	HERC1	GRCh38.p7	15:63775214	TCTGCTGAACCAGAA[C/G]TGCTCTCCGGAGAAT	8925
rs563024523	snp	A/T	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63619920	CTAGCAGTCTATCAA[A/T]TTTGTTGATCTTTTC	8925
rs563031002	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63830668	GGAGCTTGGTGAAGA[A/G]TATGTAAGAACTCTG	8925
rs563040606	snp	C/T	1.6585e-05	0.00287962	missense	HERC1	GRCh38.p7	15:63674825	CTGATTTGGAGCTTG[C/T]GGTACTCTGACTTTT	8925
rs563043473	in-del	-/TTTAC			intron-variant	HERC1	GRCh38.p7	15:63713196	GAATCAGTATCAGTA[-/TTTAC]TTTACTTTAAGTTCA	8925
rs563052726	in-del	-/AGGTTAGAGATGGCTTGTCAGGATCA	0.0490535	0.14873	intron-variant	HERC1	GRCh38.p7	15:63693569	TTTAGGTCAGGACTT[-/AGGTTAGAGATGGCTTGTCAGGATCA]AGGTTAGAGATGGCT	8925
rs563059941	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63753379	CTCCCCCTTTAATGG[C/T]TATATTTCTAACTTC	8925
rs563079556	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63790779	ACAGTAGGGTTTTCT[-/T]TTTTTTTTTTTTTAA	8925
rs563101391	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63807333	AGGAAATGGGAGGAT[A/G]AGAAGTAAAAGAAAT	8925
rs563126958	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63629534	AATCTCCAAACCTCT[A/G]TACTTAGGGTCTGAC	8925
rs563128580	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63796828	TACAATAAAGGGTTA[A/T]GGAGACCAAGGTTTT	8925
rs563131460	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63657103	TTTAGTTGATACTAT[C/T]GAACAGTTTTCCAAA	8925
rs563168605	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63663778	TCATATAGAAAAAAA[C/T]TTCAATAAATATTGG	8925
rs563172165	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63634028	AAAACACACTCCCCC[A/G]TTTCTGGGACCCTTT	8925
rs563173718	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63794529	TGACCAGCCCCAATC[A/C]TGAAGCTAACCAGAG	8925
rs563174078	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63676590	GGTGAAACCCTGTCT[C/T]TACAAAAATATAAAA	8925
rs563175767	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63792639	TTGGATGATATAGAA[C/T]GAAAGAACTCAGTTT	8925
rs563199451	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63617520	ATCCTTTGGGTATAT[A/G]CCCAGTAATGGGATG	8925
rs563211778	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63785845	AAAATTCAAAAACAA[C/T]AGGATTGATATCTCA	8925
rs563225069	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63771725	GGTGTAAGCCACCAC[A/G]CCTGGCCAGCAATCT	8925
rs563243073	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63755838	TTAATAAAAAGAGAA[G/T]ATATGAGCTCAGTTT	8925
rs563244268	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63619231	ATTTTGTCAAAGGCC[G/T]TTTCTGCACCTATTG	8925
rs563244797	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63661694	AAATCTACAGTTCCC[A/C]AGACTTAAGGTATGA	8925
rs563258863	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63720343	ATTCAGTAGATTTCA[A/G]ATGGGGGTGGGAGAG	8925
rs563261599	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63825507	AAATTTATACAATAA[A/G]TAAGTAAGTAAGCCT	8925
rs563262828	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63764749	GCAGTGGTTAACTGT[C/T]TCTCTAAAACAATAA	8925
rs563262865	snp	C/G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63686632	CCTACAAATATTTAT[C/G/T]ATGTATCTACTATGA	8925
rs563276388	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63819198	CTTTGGTTGCAGAAC[C/T]AGAACCAGTTCATTT	8925
rs563279138	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63728484	ATCTAATGAGGAAAG[A/G]TTTCAGTTTCACAGT	8925
rs563300278	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63811757	GAGCTTGCAGTGAGC[C/T]GAGATCGCGCCACTG	8925
rs563303394	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63693154	CTGCACTCCAGCCTG[A/G]GTGACAGGGTGAGAC	8925
rs563318257	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63805854	AAGCTGAGGCAGGAG[A/G]ATTGCCTGAGCCTGG	8925
rs563388632	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63691559	AAAATACATATAACT[A/G]TAATAAGATCAGTTG	8925
rs563395602	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63657606	CTTTTCAAATCACTT[C/T]TGCTAAACAGAGGTT	8925
rs563454326	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63639865	TATACAACTAAAGCA[C/T]TAACAAAGTACCTAT	8925
rs563489663	snp	C/G	0.000740706	0.0192303	missense	HERC1	GRCh38.p7	15:63615872	CAGGGATTATAGGAA[C/G]CATTTTGCCATCAGC	8925
rs563507309	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63832672	AGCTAACAATCATTT[C/T]GGAAAAGGGCCCAGT	8925
rs563523730	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63820764	CTCAAGCAGTTCTCC[G/T]GCCTTGGCCTCCCAA	8925
rs563532048	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63609828	TTAAACTCCAGTCCA[A/T]CCATTCAACTGACGG	8925
rs563547571	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63644907	GGGATATAGTAATGA[C/T]TTTTTTAGTAACCAA	8925
rs563565704	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63670998	CCTGAGGTTGGGAGT[C/T]CGAGACCAGCCTGAC	8925
rs563578278	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63654883	CAAAAAAAAAAAAAA[C/T]TTATTATACAACAAT	8925
rs563606151	snp	A/C	0.000415534	0.0144081	missense	HERC1	GRCh38.p7	15:63678221	TTTTTTTGTTAATGC[A/C]GTAAGTCCAACGGTC	8925
rs563609521	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63787747	TACAGCAAGACTCCA[A/T]CTCTTTTTAAAAAAC	8925
rs563626665	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63749059	TAATTATTTTAATTT[C/T]CTCTTGATATGCAGA	8925
rs563632552	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63717324	ATCCACAAATACTAA[C/G]TCAGTATATGACAAA	8925
rs563644724	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63815627	CTGAAAAATGTCTTA[C/T]TTACCTATCAAAAGT	8925
rs563654178	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63686091	GAAGAAAATGTGTTC[C/T]GTGTGACTCCTTATG	8925
rs563666194	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63736775	CCATGCCCAGGTAAT[C/T]TTTGTATTTTTAGTA	8925
rs563667945	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63699584	ATTCTCACTGACTGT[A/G]TCATGTGCATATTTA	8925
rs563677180	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63645410	TAAGACTACTGAGAA[C/G]CCACACTTAATGCAG	8925
rs563686251	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63745410	AGCCCTCAGTGGCAA[A/G]CCTTGCAGGAATTCA	8925
rs563694988	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63824517	CCAGCCTGGGCAACA[C/G]AGTGAGACTCCATCT	8925
rs563710227	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63833547	CTCTCGGCCCTCTCC[A/G]CGGGCGCCTCGGCTT	8925
rs563714220	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63651099	CACTTCCTCTCTAAT[C/T]TGAAGCACACAGTGC	8925
rs563739616	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63742511	TTGCCCCAGCTAGAA[C/T]AGAAATGGCAGGAGT	8925
rs563747409	snp	A/G	0.00993419	0.0697739	intron-variant	HERC1	GRCh38.p7	15:63775805	CACTTTGGGAGGCCA[A/G]AGTGGGCAGATCACT	8925
rs563752152	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63610332	GGGAGGTGCCACTAG[C/G]TGGCTCTGATGACCT	8925
rs563782401	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63729886	AAAAATTAGCTAGGC[A/G]TGGTGGTGGGTGCCT	8925
rs563798621	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63780122	TGTACTTTCAGAAAA[C/T]AGACATTTTTATGAA	8925
rs563799150	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63796080	ATTTTTAAGAATGTT[A/G]GCACAGGTCTTTAAA	8925
rs563800298	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63700357	ACCCAATTAAATATG[C/T]ATAAAAATTATATCA	8925
rs563806205	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63679190	AGAACATGACAGAAA[A/C]TACTTTGGGCTGCAA	8925
rs563811379	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63660558	TAATTAAAAATATTG[C/T]CATGGGTCCAACAAA	8925
rs563814040	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63609783	CGCCATGGCTGCCTC[A/G]CACAGCTCACATAAG	8925
rs563833996	snp	C/T	0.000399281	0.0141238	missense	HERC1	GRCh38.p7	15:63696156	GGCCACTCTCTCCCT[C/T]GCCTCCTGTGTGTCC	8925
rs563837507	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63750014	TCTGAAAATAAAAAT[A/G]ACTGGTCATAGAAAA	8925
rs563843272	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63707545	CATATATGACTTAAG[C/T]TTGTGCATAGACTTG	8925
rs563859241	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63777768	GACTCTCACACCCAG[A/T]TTCCACATGAATTCT	8925
rs563896035	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63711679	ATTTCAGAATTACAC[A/T]TGGAGCTTATAGATA	8925
rs563907825	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63816149	GTTCCTCAAGATGTT[A/T]TAAGGAGGAAAAAAG	8925
rs563909601	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63646645	TCTCTAGTAAAAATA[C/T]AAAAAAAAAAAAATT	8925
rs564007184	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63638976	TTATTATAAACACTT[C/T]CACTATCACTATCAC	8925
rs564008528	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63682464	GTGGGAGGGGAAAGG[G/T]TTCAAAAACCCCTGA	8925
rs564016134	snp	G/T	0.0111196	0.0737302	intron-variant	HERC1	GRCh38.p7	15:63780639	AGGCAGGAGAATGGT[G/T]TGAACCCGGGAGGCG	8925
rs564018971	snp	C/T	0.00278303	0.0371991	missense	HERC1	GRCh38.p7	15:63689696	AAAATAAGCGCTCAA[C/T]AATCTGTTTTATTGA	8925
rs564021994	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63703542	GCAAATGCTGTATGA[A/G]GGAAAACATTTTACA	8925
rs564046503	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63615308	CTGAATAGGGTTTGG[A/C]ATATAAATACAAAGG	8925
rs564047287	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63722938	AGTAAAATGATTACC[G/T]ATAAATGTATTATAT	8925
rs564058430	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63710455	TTAGACAGTTATTTA[C/T]AAATTTAAAAATAAT	8925
rs564067959	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63822717	TAAGAGGTCAAGTGA[G/T]AAAACAAGGAAACCA	8925
rs564090335	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63614528	ACTAGGCTAAAGATA[C/T]CATTTTTCTGATGGG	8925
rs564090680	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63813468	TAATCTAGGATAGTG[C/T]GAAAGGGTTTTTTTT	8925
rs564103001	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63746030	TTCTTTATTTTTTTA[A/G]TTTCACTCTAATCTA	8925
rs564139873	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63745578	AATTGTTGTGTTCTC[C/T]CTCCCCAAGCACCCA	8925
rs564144230	in-del	-/A	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63748699	TAACTATTGATAAAT[-/A]TTTTTAATTGGTTAG	8925
rs564145088	snp	A/G	1.65616e-05	0.00287759	missense	HERC1	GRCh38.p7	15:63733040	TTCCGTAGCCAGTAC[A/G]CACAGAAGATAGGTC	8925
rs564150196	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63613467	TTCATAAATACTTCT[C/T]TGCTCTTGGCCAACT	8925
rs564151621	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63719491	CCTCCAGGTTTTACT[C/T]GGGGAAAAATGAGAA	8925
rs564151753	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63711448	CTGGGAGTATGAAGT[A/G]GAAGCACAGAGATAT	8925
rs564169448	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63683420	GAGAGGCAAGCTCTA[C/G]ATGGAGATATAGACA	8925
rs564175413	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63693762	GGTCACAACATGAGG[G/T]TTAACAGACTCTAAG	8925
rs564197558	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63790937	AATTTGGGTATATAA[A/C]AACTGAAAGATATCT	8925
rs564201289	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63752759	GCTCCACTAAGATTT[A/C]TCTGGGTCACATATG	8925
rs564212490	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63612888	TATTCCTAATCATAT[A/G]TGCCCATGTGCTGTC	8925
rs564230783	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63736085	AGGAAAAAACAGCAT[C/T]AAAATTTTGGAAACA	8925
rs564233108	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63783901	TGAAACCCCGTCTCT[A/G]ATAAAAATACAAAAA	8925
rs564240542	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63703023	GCAGGAGAATTGCTT[G/T]AACAGGGACCCGTGA	8925
rs564262250	snp	A/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63635034	CAATGCTTTTAAAAA[A/T]TTTTTTTTTTAATTT	8925
rs564274265	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63634225	AATCAGTATGAAAGA[C/T]AGAGGAAAAGTATAC	8925
rs564280129	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63763442	ACATAAGGAACTGCA[C/T]CATGAGTAATCTATC	8925
rs564283138	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63817444	CAGAGGCCGGGTGTG[G/T]TCGCTCACACCTGTA	8925
rs564296728	snp	A/G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63642603	TCAGCCTCCCCAAAG[A/G/T]GCTGGGATTACAGGC	8925
rs564306908	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63791807	GAATAAAGAAGTTGA[C/T]ATTTCTTCAAATATT	8925
rs564307739	in-del	-/AAG			intron-variant	HERC1	GRCh38.p7	15:63685742	GAGTAGACTGTGCAA[-/AAG]AAGGAGTTAACACAA	8925
rs564317242	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63768453	TGTTTAAAAGTAACT[A/G]GTCCCTAGACATACA	8925
rs564319098	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63776704	GGCATGGTGGCTCAC[A/G]CCCATAATCCTAACA	8925
rs564337001	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63621083	GATGCAGTTTCTTCC[C/T]AGCCTCGATGGTCTT	8925
rs564340531	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63762908	TGGCTCCTTGCTTCT[A/C]GCTCTCCTAGGCTCC	8925
rs564349022	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63760779	AAGAAACTGTAATTT[A/G]GGGACATTTTCCTGA	8925
rs564349063	snp	C/T	3.31857e-05	0.00407329	missense	HERC1	GRCh38.p7	15:63675031	GAAGCCGTCAGGCCT[C/T]GGAATCGCGCCACAT	8925
rs564365132	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63732305	CGCGCCTGGCCTGAA[A/G]GGGTTTTAATTTAAT	8925
rs564370144	snp	C/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63741221	TTTAGTAGAGACGGG[C/G]TTTCACCATGTTGGT	8925
rs564380012	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63776252	TAACAGTTTTGGTTA[C/T]GGTTGGATATCTCAA	8925
rs564385460	snp	A/G	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63682843	ATGATTAAAAAAAAA[A/G]AAGATGCAAAGGCTG	8925
rs564391667	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63709303	GCATGAGCCACTGCG[C/T]CTGGCCCAATCTTTT	8925
rs564408437	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63747238	GCGGAGGTGGGTGGA[A/T]CACCTGAAGTCAGGA	8925
rs564426996	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63675466	TCAACCCTGCCATCA[C/T]AGTGCAAAAGCAGCC	8925
rs564475566	snp	C/T	1.67036e-05	0.0028899	synonymous-codon	HERC1	GRCh38.p7	15:63756587	AGATCCTTTAGAAGA[C/T]GAAACCTTTTTAATG	8925
rs564477854	snp	A/C	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63704785	GCTCTGTCGCCCAGG[A/C]TGGAGTGCAGTGGTG	8925
rs564492924	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63797831	TTATCACAAAAATCC[A/G]TAAGATAGTTATTAA	8925
rs564493591	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63624451	CCTGTAGTCCCAGCA[C/T]TTTGGGAGGCTGTGG	8925
rs564496132	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63655071	TCCAAAAGCCAGTAT[C/T]GGCTGGGTGTGGTGG	8925
rs564499263	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63661190	AACTGCTGGTATGTA[G/T]GTACACACATGCTTA	8925
rs564511211	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63715484	CTCCATTTGGATCTT[C/T]TTCCTTTTGTTTAAA	8925
rs564534539	in-del	-/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63797412	AGAATCTAAGATTGG[-/T]TTTTTTTGTGTTATC	8925
rs564537665	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63668672	CAGGGCAAAAAAATA[C/T]CACCAAGGATAAAGG	8925
rs564538560	snp	A/C	0.00478085	0.0486577	intron-variant	HERC1	GRCh38.p7	15:63649157	GAGGAGATCGAGACC[A/C]TCCTGGCCAACATGG	8925
rs564554972	snp	C/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63729179	TAAGACTTTGGAAAG[C/G]CAAGTGTTCTTACTT	8925
rs564557357	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63623568	AAGCTGTTGCTCTAA[C/T]TTACCTACGTATCAC	8925
rs564584918	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63792388	TCCACCTCTGGAAGG[A/T]ATACAAAAAGAATAT	8925
rs564619121	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63755506	GAGTTCAAGTAAGTG[C/T]TGAAATACATGCCTG	8925
rs564621341	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63698361	AGGCAGAGGTTCCAG[C/T]GAGTCAAGATCTCAC	8925
rs564623790	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63763007	GCGCCTGCCCTTTTG[A/C]CCTCCACATTCTCAC	8925
rs564638799	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63699933	CCTTTCGTCATGACA[C/T]ACTCTCATCATTGGT	8925
rs564661124	snp	A/C/T	6.62771e-05	0.00575628	missense	HERC1	GRCh38.p7	15:63698912	TCTGACTCAAAGGAA[A/C/T]AGGAGGAGTTGCATA	8925
rs564661757	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63705239	GTACCCTGCAACTTC[A/G]AATTCCTGGGCTCCT	8925
rs564666918	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63799054	TTCAGAACTAGGTCA[C/T]ACTTGCACATTTAAT	8925
rs564668458	snp	A/G	5.91804e-05	0.00543936	intron-variant	HERC1	GRCh38.p7	15:63622925	AATTTTTTGAGAAAT[A/G]ACAATCAAATGCATG	8925
rs564675188	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63830633	CTGTATTATGGTTAT[A/G]TAAGTTGTTAACATT	8925
rs564681720	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63758422	CAGTTTTAGTCTGGG[A/C]ATTTTTTATACATAT	8925
rs564694383	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63733936	GGGAGGCCAGAGCAG[A/G]AGGATCATTTGAGGC	8925
rs564695769	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63707636	AAGAAGGCCCGGAAG[C/T]GACAAAACAAGGCCG	8925
rs564697648	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63741097	GCAATGGTGCGGTCT[C/T]CACTCACTGCAACCT	8925
rs564700595	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63649558	GGGGGCTAGGAGATA[A/C]ATATCTTTCAATTCA	8925
rs564705470	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63792589	CATAATATATGGTGT[C/G]GTTTTAATGTAAAAT	8925
rs564713627	in-del	-/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63697187	TTTCCTTTTCCAGGA[-/T]TTTAATCCTAGATAC	8925
rs564734929	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63744786	GACAGGTCTAGAAAT[A/G]CCATCTAACAATCAA	8925
rs564759184	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63637446	GGGCAAAGGTTTGTA[C/T]GACCAAACCTACATT	8925
rs564777069	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63671563	CAGTAATTCTCAAAG[G/T]GTACGCTGAAGCCAC	8925
rs564829919	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63750229	CAAAACTGATGTTTA[C/T]TATTTAGTTTTAGAA	8925
rs564854230	snp	C/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63766366	GCTGAGGTGGGCAGA[C/T]CACTTGAGGTCAGGA	8925
rs564878128	snp	C/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63617574	TTCTAGATCCATGAG[C/G]AATCACCACACTGAC	8925
rs564888102	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63702266	AGAAACATTTACATT[C/T]GCTTTTCTTTATATC	8925
rs564897611	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63800736	GAAATACATACTTGG[A/T]GTTCGTAATTTCCTT	8925
rs564909571	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63807034	TACAGGCATGAGCCA[C/T]CACACCCGGCCTGAG	8925
rs564919570	snp	A/G	2.07881e-05	0.00322391	intron-variant	HERC1	GRCh38.p7	15:63664632	AACACAAAGTTTTTG[A/G]AACCATTATGGAAAG	8925
rs564967976	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63787873	AGGCATACTGGGGAG[A/G]CCGCCTGAGTCCAGA	8925
rs564980912	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63706735	TTTTTTTTTGAGACA[A/G]GGTCTCACTAAGATA	8925
rs564984859	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63774528	ACCAACCATATATTA[C/T]CAACATGCATAAAAG	8925
rs564994471	snp	C/G			missense	HERC1	GRCh38.p7	15:63645088	ACATACTAAGCCACT[C/G]TGACAGCCACTTAAA	8925
rs564999807	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63639569	TTATATTTGTCTGTT[G/T]CATATTGTATCAATG	8925
rs565001370	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63744059	TGGGAGAATTCTCTG[C/G]ATTATCAGGCAGAGA	8925
rs565017063	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63827507	TTCCAGGATATACTA[C/T]TGAGTGAAAAAAAGT	8925
rs565019858	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63630847	AAAACATCACAGGCT[C/T]TTTATTCATAAAAAT	8925
rs565030889	snp	C/G	6.47585e-05	0.00568991	intron-variant	HERC1	GRCh38.p7	15:63694264	GAATTCTAAAATGGA[C/G]GAAGACCAGACTTCA	8925
rs565040898	in-del	-/TTGTT	0.00927747	0.0674734	intron-variant	HERC1	GRCh38.p7	15:63681180	ACTAGGTGTATTGTT[-/TTGTT]TTGTTTTGTTTTGTT	8925
rs565071873	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63610515	GTTTCCAGAGCTGAG[C/T]AGAAATGAGCCATTT	8925
rs565099027	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63794464	CCTTCCCAGAGGTTG[A/G]GGATGGGGCTGAAAG	8925
rs565117190	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63685574	CATGGCTTTTTAAGA[C/T]AGACCTGTTGGTTAA	8925
rs565121092	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63731724	GACCCTGAAGAGCCA[A/C]AGGAAACAATATTAA	8925
rs565125374	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63651979	AGGCAGAGGTTGTGG[C/T]GAGCTGAGATTGCAC	8925
rs565132812	snp	C/T			synonymous-codon	HERC1	GRCh38.p7	15:63659863	ATTTAAACCAAGCGG[C/T]CCAGCAAGTAATTCA	8925
rs565139400	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63814820	AGAATCAGCTCTGCT[A/G]TGGAAAATATGAAAC	8925
rs565158891	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63802375	CAAATTGTTTTTGCT[A/G]CATCAATAATGAGAA	8925
rs565172998	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63701401	TATGGAATGGCTGAC[A/G]AAGCCCAAAATTAAA	8925
rs565184725	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63803481	GGCTGGAGTGGCAGC[A/G]ACACAATCATAATTC	8925
rs565203493	snp	A/C/T	6.62782e-05	0.00575633	missense	HERC1	GRCh38.p7	15:63666022	CGCCACTGCCTAGAA[A/C/T]GGCTGCTCCAGGCCT	8925
rs565211985	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63700643	TAGAAAGAATTATTA[A/T]GATTTAAAAAGGCTT	8925
rs565217360	snp	A/G	1.65737e-05	0.00287864	missense	HERC1	GRCh38.p7	15:63775151	CGAACACCCATTTCT[A/G]TAAGTGCATCAGTGC	8925
rs565218537	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63708250	CTCAGGCCTCAGAAC[C/T]AGAAAAATCTGGTTC	8925
rs565221542	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63767063	CTGGAGTGCAGTAGC[A/G]CAGTCTCGGCTCACT	8925
rs565221616	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63823205	CTCCCCTCTGTGTGT[A/C]CATGTTTTCTCATCA	8925
rs565232002	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63797717	GCAATGTAGTGGTCT[C/G]TGTTAATTGATTTTG	8925
rs565241726	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63673363	TACTTATATACACCA[C/T]GTACCTCTCTCTCTC	8925
rs565246409	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63821723	CAGAGTGATACCCTG[C/T]CTCAAAAAAAAAAAA	8925
rs565253221	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63687130	ACCTACACAGAATGA[C/T]GTATATAGGAGATCT	8925
rs565253862	snp	A/G	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63767602	ACTGGGGAGGCTGGG[A/G]CAGGAGAATCACTTG	8925
rs565273097	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63632099	ATGGGTCCATTCAAC[A/G]TAACTAAAACTAAAT	8925
rs565281250	snp	G/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63822149	TAAACCCTGGGAGTC[G/T]GCCTGGCCCGGTCAG	8925
rs565294978	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63675967	GCAGTGCAGTGGTGC[A/G]ATCTCAGCTCACTGC	8925
rs565338360	snp	A/G	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63738572	AAATTTTTTAAAGAA[A/G]AAAATTCAGAGAGGG	8925
rs565352647	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63788745	AACGTGGTGAAGCCC[C/T]GTCTCTACTAAAAAT	8925
rs565359204	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63687430	GTAATCCCAGCTACT[C/T]AGGAAGCTGAGACAG	8925
rs565371356	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63827108	AGAGGTTAAGAAACA[A/T]CTACACAGTCAAGTC	8925
rs565375500	in-del	-/AAGAACCATTT	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63614711	TGACTGTATTATCAA[-/AAGAACCATTT]AAGAACCATTTTTGG	8925
rs565389101	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63781363	CCATTTTTCCAAAAG[A/T]ACGTGTTCACTTCAT	8925
rs565403516	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63776368	AATAAATGGTAACTC[C/G]ATCCTTCTAGTTCCC	8925
rs565413805	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63778753	ACTCAAGTGCATACA[A/G]AGCTATTGCAGAAAA	8925
rs565422980	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63673794	CAGTGGCACAATCTC[A/G]GCTCACTGTAACCTC	8925
rs565431838	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63761306	AGAGACAGGCTGGGC[A/G]CCATGGCTCACGTCT	8925
rs565432433	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63675207	AGACAAAATAAGGTG[C/T]ATCATGTACACAATA	8925
rs565433403	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63619164	TACTATTTTGAGATA[C/T]GTCCCATCAATACCT	8925
rs565439834	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63823695	ATATAACAAATGTCC[A/G]AATGTCTTTGGGCAT	8925
rs565447847	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63709747	CTGTGTAGGAGATAT[C/G]AGGGGCATTTAGGAA	8925
rs565454206	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63808621	AAAGGATCTTTGGGG[A/G]AAAAAAAGAGTAAAG	8925
rs565458947	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63681983	CGTGTGGAGTCTGAC[A/G]AGTCCTTCTAGTGAA	8925
rs565468893	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63633161	TTTTATGGGCGACAA[C/T]AACTGCTTTATATGT	8925
rs565485426	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63717183	ACTTTTACAGAGATG[A/G]GGATACAGAGTAGTC	8925
rs565493368	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63618546	TCTGTGAAGAAAGTC[A/C]TTGGTAGCTTGATGG	8925
rs565499976	snp	A/C			missense	HERC1	GRCh38.p7	15:63754642	CGACTATTGCTGTCA[A/C]CATGACCTTGGATAA	8925
rs565507349	in-del	-/CTCCT	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63739442	CTCAAGTGATCTACC[-/CTCCT]CTCCTCGGCATCCCA	8925
rs565508565	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63697972	TATTTGGGGGAAGAT[A/G]CTTTAAGGCTATGCA	8925
rs565514513	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63804477	TGTCATTCCAGCTAC[C/T]TGGGAGGCTGAGGCA	8925
rs565547731	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63704980	CCTGACCTCGTGATC[C/T]GCCCACCTCAGCCTC	8925
rs565577451	snp	C/T			missense	HERC1	GRCh38.p7	15:63632736	TATACACATGACCAT[C/T]TTTGGTCAAAGCAAC	8925
rs565605249	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63634462	GGGTTTAATAGCAAG[C/T]GGTATTAGTATGTTA	8925
rs565610597	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63815198	ATTGTCTAAAAGTTA[A/C]ATATGTCCGTTCCCT	8925
rs565617538	in-del	-/AC			intron-variant	HERC1	GRCh38.p7	15:63807855	CCACTTATACTTCCT[-/AC]AGTTACTAATTCAAA	8925
rs565628550	snp	C/G	1.65636e-05	0.00287776	missense	HERC1	GRCh38.p7	15:63716384	CCGGTCTCTCTCAGC[C/G]TGTTCTTCCATTTCA	8925
rs565646430	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63636486	ATGCTGGCCAGGCTG[C/G]TCATGAACTCCTGAC	8925
rs565659362	snp	A/G	0.00199481	0.0315187	intron-variant, downstream-variant-500B	HERC1	GRCh38.p7	15:63668862	ATAATAGACAGAACA[A/G]GTAGACAAAAAAACC	8925
rs565673085	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63831333	ACTGATCTTAAACTC[A/C]TGGGCTCAAGCCATC	8925
rs565683586	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63627494	GCCTGGCCAATATGG[C/T]GAAACACCATCTCTA	8925
rs565688568	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63831212	CCCAGGCTCAATTGA[A/T]CCTCCCATCTCAGCC	8925
rs565692592	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63824409	TGTGGTGGCAGGCAC[C/T]TGTAGTCCCAGCTAC	8925
rs565731697	snp	C/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63727273	AGAGCAAGACTCCAT[C/G]TCAAAAAAAGAAAAA	8925
rs565754902	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63614926	GAAGTATGTGATATA[C/T]CTTGAGGAACTTCAA	8925
rs565772029	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63768597	GCCAACTCTAGTGAT[C/T]ACCAAAACAAAAACA	8925
rs565783920	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63743889	TGAAGAGTTAGGTAT[G/T]TATTGTAGTCTTCAC	8925
rs565794628	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63816381	TTTAATAAAAATATG[C/T]TGTCTTATGTAAACT	8925
rs565805964	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63823642	AGGATGGTACATAAC[C/T]AGTGCCATCCTACAT	8925
rs565816710	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63763153	TCTTTTTCTCAATCC[G/T]TTGAATCCACCGGAC	8925
rs565827948	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63691272	GGAGTTCAAGACCAG[A/C]CTGGCCAACATGGTG	8925
rs565850974	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63830889	AAATCGGATCTGGCA[C/T]CTAGTAAGTAAACAA	8925
rs565896899	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63742471	TTTTCAATCTACATG[A/C]GTTTTATTTCATTAT	8925
rs565912981	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63636804	TTTTACAAGTGGGAA[A/C]ACTGAGTCACAAAGA	8925
rs565927025	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63747110	TAAACGTCTATGAAT[C/T]CTCGGATCATAAAAG	8925
rs565934427	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63622006	GTCAAAGTCATTCTC[C/T]GTCCAGCTTTGTTCC	8925
rs565937884	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63785256	TAGCAAGACATTACC[A/T]TGACAAAATGTTTAA	8925
rs565963711	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63723897	TTTTCAGTGTGACAT[C/T]TGACATTCAGAATTC	8925
rs565972640	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63734220	TATTACACTGCAAAT[A/G]AGTACCAATTTTTTT	8925
rs565980484	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63610901	GGAGAGGCACTCCTA[A/C]CTGAATGCAGTAAGT	8925
rs565986847	snp	C/T	0.000168302	0.00917184	intron-variant	HERC1	GRCh38.p7	15:63660941	ATATATAAAAAAACA[C/T]GTAAAATAAAGAAGC	8925
rs565989930	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63727972	TGAACACCTACCTGG[C/T]AGCTGATGTAGTATC	8925
rs565995594	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63719967	TTGATGCCATAAAAG[A/T]ATATACTGTGAATAC	8925
rs566003246	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63792103	TTGACCAATATTCTC[C/T]AACCTTAATGTCTTA	8925
rs566010181	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63621390	ATGTGCTTCCCTTTG[C/T]GGGTAACCCGACCTT	8925
rs566035373	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63658328	GTATGCAGTTTACTC[A/G]GTTGTGATAATGGCA	8925
rs566038931	in-del	-/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63811564	CTGTAATCCCAGCAC[-/T]TTTCGGCGGCCGAGA	8925
rs566040538	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63714729	ATTTTTTGTATCTTT[A/T]GTAGAGATGGGGTTT	8925
rs566060381	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63735214	GCAAGAAAGTATAAA[C/T]GTGAAAGGAGTCACA	8925
rs566083991	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63827297	TATAGCGGTGCACAC[C/T]TGTAGTCCCAGCTAC	8925
rs566101054	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63786041	GAAAAAAATGAAAAC[A/C]ATCAGCTAACAAAAT	8925
rs566115707	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63643582	TTAACATGCATTAAA[A/G]TAAAGATAAATTATA	8925
rs566150802	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63649245	GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	8925
rs566172408	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63740940	ATGATGTCCAATTTA[C/T]TTTTCCTTTGGTTGT	8925
rs566205111	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63608983	ATGTTGGTTTATGTT[C/T]TTATAACATCTATGT	8925
rs566209048	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63828654	CAGTACACCTTTTTA[A/T]ACAGTAGTGTTTAGT	8925
rs566247265	snp	A/G	0.00279162	0.0372561	upstream-variant-2KB, utr-variant-5-prime	HERC1	GRCh38.p7	15:63833964	GTAAGAGGCGGCGGC[A/G]GCAGCGGCGGCGTCA	8925
rs566255461	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63611038	GTTCTTGGAGGAGAT[G/T]ACTGGCATTGGGCTT	8925
rs566265460	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63812812	AAAAATTATTAAGGA[A/G]AGAAATCAAAGATAA	8925
rs566265629	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63629683	TGCAACCACAATGAC[A/G]AGCAGCTTCCTTGTC	8925
rs566274307	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63701647	CTGCTGAGCCCTAAC[A/G]GATGAAATTAACCCA	8925
rs566298062	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63717950	GAAAGCCTATTTTCC[-/T]AACATTCAGCTAAAA	8925
rs566317824	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63670638	CAAGGGGGCATGATT[C/T]TACCACTGAATCCCA	8925
rs566328556	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63637725	AAATGATTCCACGTA[C/T]ACATAGAATGCTTTT	8925
rs566344031	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63738747	CAATCTATCTCCAAG[C/T]ATTCTTCTAAGATGC	8925
rs566348539	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63778926	AACTGAAAGCAGAAA[G/T]AGACAAAAAGAAAGA	8925
rs566356504	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63670033	AGGGGTAATTTGGTA[C/T]GTACAGTTACAGTGC	8925
rs566379836	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63685116	CTTGTCAAGTCTGTC[A/G]AAAGACCACAGTGGG	8925
rs566385180	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63771217	AAAGAAAAGAAACAC[A/G]GGTTCTGGAGACCAA	8925
rs566390141	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63731409	GCAGTTAGTATTTTA[C/T]TTCCATTTCCATATA	8925
rs566421691	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63808081	TTCTTCTTTTGTATT[C/T]CTTTATGGAAGTTTA	8925
rs566426212	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63763376	ACACCTGAGACTGAT[C/T]AAGCCTCTGGATCCA	8925
rs566439563	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63648500	GATTGTAAGTCACCA[C/T]AGGTTCTTTCCTTTT	8925
rs566454099	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63743696	TCTCTGTTAAATTTA[G/T]GTGATAGGATTCTGA	8925
rs566483598	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63752829	TCAAACAGAAGAAGA[A/T]ATTTCATTTTAGCAT	8925
rs566496349	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63611715	TAGGGAAGGTTGTTG[A/G]TTGTAGTATGCTCTC	8925
rs566498342	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63788870	ACAGAGCAAGACTCC[A/G]TCTCAAAAAAAAAAA	8925
rs566501363	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63786194	TGGAGGCCAGGAGTT[C/T]GAGGCTGTAGTATGC	8925
rs566503209	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63732440	TTATTAGCACTGAAT[C/G]ATAATGATCTGGCTT	8925
rs566508234	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63646296	TTTCTGACATTACTG[G/T]GAGCATTTGAACAGG	8925
rs566542526	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63652145	CTTAAAGACCTATAG[C/T]AAATTAGCCTACTGT	8925
rs566544955	snp	G/T	0.00636936	0.0560724	intron-variant	HERC1	GRCh38.p7	15:63619308	TATGTTTATTGATTT[G/T]CGTATGTTGAACCAG	8925
rs566562265	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63701615	TGCCAGGTCAGTCTT[A/G]GCCTCCTAGCTGTAG	8925
rs566562902	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63751385	CATCTAGGTTTGTGT[A/G]GTACTCTCTACAATG	8925
rs566575519	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63653059	CTGAGACCTATTATA[A/G]TCTTTACTAAATATG	8925
rs566605802	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63760533	GAATTAGAAATAAGA[A/G]AAAAAAATCATTTTG	8925
rs566616762	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63774056	TTCCCTTCATTCTGG[C/T]CTCTACTTTAATGTC	8925
rs566626890	snp	A/G	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63673568	AAACATTGACTGAAC[A/G]AATCTCATTTTTATT	8925
rs566640331	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63761532	ATAGAAGCTGCAGGG[A/C]ACTATGATCACAGCA	8925
rs566640434	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63752310	CAGAATAAGTGGCCA[C/G]CTCACTTTTTTACTG	8925
rs566643008	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63821204	GGGTGAGAGGATCAC[C/T]TGAACCCAGGAGTTT	8925
rs566652448	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63618647	TGAGCATGGAATGTT[C/G]TTCCATTTATTTCTA	8925
rs566674396	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63808248	TCTGAATAACGGCTG[C/T]TATCAAACTTGGGTG	8925
rs566706302	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63613068	AATCTGAAAAGTACA[A/G]AGAAGAAAGTAAAAA	8925
rs566716395	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63697612	GGCATCCACCACCAC[A/G]CCCAGTTAATTTTTG	8925
rs566725672	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63631829	TACAGGTGTGAGCCA[C/T]GGCGCCCGGCCCTCC	8925
rs566727656	in-del	-/TT			intron-variant	HERC1	GRCh38.p7	15:63817353	AAGAGATAGACACTC[-/TT]ATCTTTTAAAAATCA	8925
rs566744091	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63770160	CGGGGCTTGCTCTCC[C/G]CACAACTCAATCGCT	8925
rs566751525	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63783386	CTCTTTGAAGGATCA[C/G]AGGACTCTCAGCATT	8925
rs566759463	snp	G/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63710059	GCAGATGAACTACTA[G/T]GGCAAAAATGCAGAC	8925
rs566763819	snp	C/T	1.66333e-05	0.00288381	missense	HERC1	GRCh38.p7	15:63774747	AGTCAAAGCTGATCA[C/T]TCCTTCCTGGCTTGA	8925
rs566769072	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63681489	GGCATCAGCCACTAC[A/G]CCTAGTGTGACTATT	8925
rs566788541	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63726796	AATTATTTCAGTGAA[C/T]AGGAATAAAAGAAAG	8925
rs566834069	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63653498	CTCAGAGACCCCATG[A/G]GTTAGATTAAAATAG	8925
rs566835159	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63666984	GGTCGGTGATTTCCC[G/T]GATTAAAATGGCCCC	8925
rs566836282	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63666553	CATAGTCCTCAATTT[C/T]CTAGTATTGTCCAAG	8925
rs566863002	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63648375	GGATTCCATGTAACA[C/T]ACTTTTTAAAAGTGT	8925
rs566874445	snp	A/G	9.94299e-05	0.00705018	missense	HERC1	GRCh38.p7	15:63612513	AGGAGGGACAGCAGC[A/G]GCACAGGAACAATCC	8925
rs566899028	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63717375	GAGTTTGGTTTTTTA[A/T]ATCTAAGGACTAAAT	8925
rs566942654	snp	C/T	1.72785e-05	0.00293921	intron-variant	HERC1	GRCh38.p7	15:63659699	ACAAATTATAGTAGA[C/T]GCTATAAAATCAATG	8925
rs566970889	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63828832	GAGTGGTAAAGAAAA[C/T]AACTAACCTAAGTAA	8925
rs566971006	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63668647	CTATAACATCAGAGA[A/G]AGCAGATTTCAGGGC	8925
rs566975484	snp	A/G	1.6727e-05	0.00289193	intron-variant	HERC1	GRCh38.p7	15:63666319	AAGCTAGGACTTCTC[A/G]TATCTGTATACACTG	8925
rs566989469	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63739988	TGATGTCAGCTCACC[A/G]CAACCTCTGCCTCCC	8925
rs566991772	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63702584	ATCGTACAACCATAG[A/C]AAATCTTTTAAGTTT	8925
rs566997855	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63763943	TCACCCCACCCCCAC[C/T]CTAGATACCCAGTTC	8925
rs567004566	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63796865	CAGATGAGGCCTCCA[A/G]GTAACAGGCTTCAGA	8925
rs567019792	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63801973	ATCTCTAACACATCA[C/T]GTTTAAAACTGAACT	8925
rs567026129	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63829277	TTAAAAAAAAATCAG[C/T]GGGGCATGGTGGGTG	8925
rs567036938	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63764263	AATTAGTTAAACAGT[C/G]TACAAAAACAACACC	8925
rs567046344	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63644564	AGCTTCATGAATTTA[C/T]GTTACTCGCCTAGAG	8925
rs567069457	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835802	GGCCTCCCAAAGTGC[C/T]GGGATTACAGGGGTG	8925
rs567085976	in-del	-/ATA	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63828690	CAGTGTTTAGTAACT[-/ATA]ATGTTTCATATGCCA	8925
rs567088418	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63641409	GATAAGTTCAAGGCT[A/G]TAATCACATTCCAAA	8925
rs567091676	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63813749	AGGCAGGAGATCAAA[C/T]GCCTATCAATGTCCT	8925
rs567100382	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63762697	TTCATTAAATTGAAA[A/G]CTGGTAAATAAAGAG	8925
rs567103025	snp	A/C	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63732166	CCGCCACGCCTGGCT[A/C]ATTTTTGCATTTTTA	8925
rs567129452	snp	A/C/G	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63726769	AGGAAGAGATAACTC[A/C/G]TATCTTACACAAATT	8925
rs567146004	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835261	TCACATACGGCACAT[A/G]TTAAGTACTCATTAA	8925
rs567147479	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63688723	AAAAACCAAGATAGG[A/T]ATTAAGGTAAATGAA	8925
rs567148024	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63787449	GGCATGAGCCGCCAC[A/G]GCTGACCAATAAATT	8925
rs567156591	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63650559	AGTCCCTGAGGTTCC[A/T]GGCATATGTCACCAC	8925
rs567163753	snp	G/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63745663	TATTCAGGACTGTTT[G/T]TTCTATCTCTTCAGT	8925
rs567190005	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63828667	TATACAGTAGTGTTT[A/G]GTAGAAGCAGTGTTT	8925
rs567202479	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63696394	TCAGACATGATGAAA[C/T]TCTGTATGCCAAAAA	8925
rs567210985	snp	A/C/G	0.000111553	0.00746766	intron-variant	HERC1	GRCh38.p7	15:63615932	TCATCTAGGAACAGA[A/C/G]GAAAACAGAATTTTT	8925
rs567249333	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63706399	CTCCCTGTAACACCA[C/T]TTAAACTGTAACAAC	8925
rs567257303	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63805371	AGCATTATGCTAAGC[A/G]AAATAAGCCAGACAC	8925
rs567272238	snp	C/T	1.69052e-05	0.00290728	missense	HERC1	GRCh38.p7	15:63712845	GATTTGATCAGTCTA[C/T]AATTTGGGCTTGTGT	8925
rs567272961	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63669877	TCATGCAGCACTTTC[A/G]GTATAAATGTAATAA	8925
rs567283099	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63621878	GCATTGGTTATTCTA[C/G]TTAGCCATTCGTCTA	8925
rs567285720	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63813052	CAACTTACAATCAAC[A/G]ATATTGAGATACATA	8925
rs567299107	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63663439	AAGTAAGAGAATCCA[C/T]GCGATGCTTTATAAT	8925
rs567309581	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63720376	ATTGTCCACCCTGCT[C/G]CCAGAGGGACTGCTA	8925
rs567312768	snp	A/G	0.00438332	0.0466095	utr-variant-5-prime	HERC1	GRCh38.p7	15:63833870	CGGCTCCGGCGACCC[A/G]AGCCCGGCTCCGCAG	8925
rs567329860	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63705786	AATAATCCCAGCACT[G/T]TGGGAGGCCAAGGTG	8925
rs567332082	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63771075	GTGCCTGTAAACCCA[A/G]CTACTGGGGAGGCTG	8925
rs567333210	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63813633	CTAACAGGTCAGCTA[C/T]TAGTGTGGGAAGAAG	8925
rs567340215	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63670557	CTAATGAAGTCCCAG[A/C]CAATAGCAGGAAAAT	8925
rs567354056	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63799295	CAGTTGAGCCCAGGA[A/G]TTTGAGACCAGCCTG	8925
rs567357981	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63692046	AGAAATCACATTATG[A/G]TAAGAGAGACTGTAC	8925
rs567386064	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63779751	CCAGGCACGGTGGCT[C/G]ACGCCTGTAATCCCA	8925
rs567398436	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63767686	CTGGGAAACAAGAGC[A/G]AGGCTCCGTCTCAAA	8925
rs567416374	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63811903	TAAACATGGTTTTTC[C/T]ATTGTTAACCATGTT	8925
rs567418263	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63804805	ACACTTCACCAAAGA[C/T]ACATAAACAGCCAAA	8925
rs567427154	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63780350	AAATTATACAAAGAC[A/G]GAACAGGAAATGAAT	8925
rs567437727	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63748204	GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC	8925
rs567448655	snp	A/G	1.65638e-05	0.00287778	synonymous-codon	HERC1	GRCh38.p7	15:63644998	GAATGTTACCTGGCA[A/G]TTTGATTCCTGCTCC	8925
rs567473623	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63739709	CTGGGCATGGTGGTG[C/T]GCGCCTGCAGTCCCG	8925
rs567474053	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63699735	AATACCATTAGATTT[G/T]CCAGTGGGTATTTTT	8925
rs567492143	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63773742	AGAGATGGGGTTTCA[C/T]CATGCTGGCCAGGCT	8925
rs567505562	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63799983	GAAAAAAATATTTTT[A/G]GTTAGCCAGATGTGG	8925
rs567506170	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63735461	ATGACAAGTTGATAG[G/T]TGCAGCACACCAACA	8925
rs567532883	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63769949	ATTTTTTTCCCCTCA[C/T]ATTTGTCTGCTTAAG	8925
rs567534778	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63738083	ATTGAGGCCAACATT[A/G]TCAGTAATAAGATAT	8925
rs567543629	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63735395	ACCGGGGCCTGTTGT[A/G]GGGTGGGGGGAGGGG	8925
rs567558440	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63819767	GCCAAAACTATGTCA[C/T]TGAGGCTGGCCATGT	8925
rs567564538	snp	C/T	0.00993419	0.0697739	intron-variant	HERC1	GRCh38.p7	15:63762993	CAGCTGTAGACCATG[C/T]GCCTGCCCTTTTGAC	8925
rs567573974	snp	A/G	0.00835141	0.0640778	intron-variant	HERC1	GRCh38.p7	15:63811145	CTATAAAAGATATGT[A/G]GGAAACAAGAAAGAT	8925
rs567574187	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63721661	TAAAAATGTATTTAT[C/T]TTTGCCATTTTGATC	8925
rs567576862	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63749216	AAGAAATCTAATGTC[A/C]TTTCTATGATAGAGA	8925
rs567583244	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63831594	TTAAGATCTGAAAAT[C/G]TGAATTTTAAAAATT	8925
rs567608038	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63699151	TGAATCTGAGCAAAA[C/T]GCTTTGGTAAAAACA	8925
rs567624327	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63820375	ACTGAATACTTGGTT[A/C]TATAACAAAGTTCAA	8925
rs567652070	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63654622	CTTTGGGAGGCCAAG[A/G]TGGGAGGATCACCTG	8925
rs567656215	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63623074	TTAGGAAATCCCCCA[C/T]ATGGAAAGCATTCAT	8925
rs567660579	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63772386	TAACTATATTGTGCA[A/G]TGATTAATATCTTTT	8925
rs567668287	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63806667	GGTCTAACAAGTCTA[C/T]GGAGAAATAACAAAA	8925
rs567669716	snp	A/G	8.28137e-05	0.00643428	synonymous-codon	HERC1	GRCh38.p7	15:63630532	AGCAAGTGTGTGTTC[A/G]GCTCCAACTGCCACA	8925
rs567680413	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63683007	CAGGCATGCTGATGC[A/G]TGCCTCCAGTCTCAC	8925
rs567681081	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63819668	TAGTCTCTAAAGTTC[C/T]GTCTCATTGTCACCA	8925
rs567690036	snp	C/T	0.00597247	0.0543191	intron-variant	HERC1	GRCh38.p7	15:63729901	GTGGTGGTGGGTGCC[C/T]GTAATCCCAGCTACC	8925
rs567722859	snp	C/T	0.000399281	0.0141238	missense	HERC1	GRCh38.p7	15:63729272	TGCCATTCCAAGGAC[C/T]TTCTTTGAGCAAATT	8925
rs567734565	snp	A/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63800763	CCTTTGTGATAGGGG[A/T]ATAGGAGCATCTTTT	8925
rs567773286	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63832358	TTTTGCTTGTATAAA[C/T]GCAGGCTATGGAAAC	8925
rs567781316	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63685748	ACTGTGCAAAAGAAG[A/G]AGTTAACACAACAGA	8925
rs567781446	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63826300	CTAACCCAGAACTTT[A/G]AACTCGCGGTTTAAT	8925
rs567791127	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63765213	CTATTCTGCTCCTTT[C/T]CTCTTGCAATTTGTG	8925
rs567812996	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63759673	CTTGTATGAACTCAA[C/T]ACAATAAAGATATTA	8925
rs567815470	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63682427	GAGTAGAAAAATTAG[A/C]TTGTAGTTGCTCTCT	8925
rs567826851	snp	A/C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63690778	ATTTCAAACTATTAT[A/C/T]GCAAGAATTCTGGAT	8925
rs567853262	in-del	-/GG			intron-variant	HERC1	GRCh38.p7	15:63711259	AGCTCAGGAGTTCGA[-/GG]GGCTGCACTGAGCAG	8925
rs567863662	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63731466	ATTCCTTTCAACTTT[C/G]TTGTAACATTCCTTA	8925
rs567869354	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63617360	TTTTTATGGCTGCAT[A/G]GTATTCCATGGTGTA	8925
rs567885188	in-del	-/A	0.226484	0.248892	intron-variant	HERC1	GRCh38.p7	15:63671373	AAGCAGCTGTCTCTT[-/A]AAAAAAAAAAAAAAG	8925
rs567892824	snp	A/G	0.00676609	0.0577691	intron-variant	HERC1	GRCh38.p7	15:63703933	AAAAAAAAAAAGAAA[A/G]AAAAAAAAAGAGAAT	8925
rs567893123	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63616815	GCCACATAAGGCTAA[A/C]GTAATTAAATAAAAC	8925
rs567893544	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63657990	AACTCTCTTCTGTAC[A/T]ATCCTATTTGCCTAT	8925
rs567898559	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63810440	AAAAAAAAGAGGGGC[C/T]ATATATATGAATGCA	8925
rs567916975	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63828175	GAATATAAGAGAACA[A/C]CCACATATATTTTCA	8925
rs567922548	in-del	-/T	0.495782	0.0457324	intron-variant	HERC1	GRCh38.p7	15:63704735	ACAAATACTCTGTAA[-/T]TTTTTTTTTTTTTTT	8925
rs567924281	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63648968	GGAACACCACAGTAA[G/T]AAGAAAGCAGACTTC	8925
rs567931442	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63711010	AGGACTCTGAGCAGA[A/G]AAACGACATGATCTA	8925
rs567931582	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63724275	CAGCAGTGGAATTAT[C/T]TTTATCATGTTAAAG	8925
rs567973587	snp	G/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63758749	TCATATACAAATTAT[G/T]TAACACAGTCACCAC	8925
rs568004426	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63776292	ATCCAAAACTGAGCT[C/T]CTATTCTACCAGTAC	8925
rs568033051	in-del	-/A	0.00279887	0.0373042	intron-variant	HERC1	GRCh38.p7	15:63738556	GGTAGTTCAAATAAA[-/A]AAATTTTTTAAAGAA	8925
rs568040038	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63717576	TAAGTAGTTTCGGCC[A/C]GGTGAGGTGGCTCAC	8925
rs568044184	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63785106	AATAAATATATAAAG[A/G]CTCAAATGCTCCATT	8925
rs568060095	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63634315	AAAAATATTTCCTTG[C/T]TAAAGGACACTCTTG	8925
rs568068877	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63729965	CAGGAGGCAGAGGTT[A/G]CAGTGAGCCAAGATC	8925
rs568070735	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63633630	GGAGACAGAAGCTTA[C/T]CCTTGCAGAATTTTA	8925
rs568073982	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63724930	AGGGGTGCTGCACTG[A/G]TAAGTCATGGTTAAG	8925
rs568119948	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63613779	TCAAAGCTGCAGTGA[A/G]TGCCACTGCACTCCA	8925
rs568146882	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63828606	GGCCTCCCAAAGTGC[G/T]GGGATTACAGGCATG	8925
rs568149231	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63775717	GTTTCCAAAATTTCA[C/T]CTTACATTACAATTA	8925
rs568180691	in-del	-/TG	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63617947	AATTTTCTCCCATTC[-/TG]TGTGGGTCGCCTGTT	8925
rs568183215	snp	A/G	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63620503	GTTCTGTAGATATCT[A/G]TTAGGTCTGCTTGGT	8925
rs568183566	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63803943	CTTTCATCAAGATAG[A/G]TCAACAGAACAGAAC	8925
rs568184123	snp	C/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63822443	AGACAAAAATTAGCC[C/G]GGCGTGGTGGCGTGT	8925
rs568211755	snp	A/G	4.96948e-05	0.00498447	synonymous-codon	HERC1	GRCh38.p7	15:63713484	ACACCGATGGATCAC[A/G]GAGTTGCATGCAGCA	8925
rs568220234	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63718059	AGAGAAGCTCTTTAA[C/G]TATTTTTAAGGCAGC	8925
rs568240811	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63768526	AATTCCCTAGTTAGC[C/T]GTGAAGCATTTCTGA	8925
rs568287494	snp	C/T	5.02256e-05	0.00501102	missense	HERC1	GRCh38.p7	15:63675071	ATGGTTCACAGGGTT[C/T]CAGATTATACAATGG	8925
rs568308558	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63660889	AACACACACACACAC[A/G]AAGGTGAATTTTAGT	8925
rs568310033	snp	C/T	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63628985	AGATGGAGTCTTGCT[C/T]TGTTGTCCAGGCTGG	8925
rs568310530	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63763070	CCGTGGGGTCCCAGA[C/G]CTCAGGGCCTTTGTG	8925
rs568324306	in-del	-/AATG	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63788544	ACAATAGCAAAACTT[-/AATG]AAGCACAAAAAGTAC	8925
rs568339491	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63698213	CTGAGGTCAGAAGCT[C/G]GAGACCAGCCTGGCC	8925
rs568356561	snp	A/T	3.32851e-05	0.00407939	intron-variant	HERC1	GRCh38.p7	15:63642914	GATTTCTAAAGTTCC[A/T]TACAAGCTTACACCC	8925
rs568364482	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63697882	ACTCTCAAGGAGAGA[A/G]GAATTAATCTCCACT	8925
rs568367693	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63667131	GGCCATAAGCTCAAT[A/G]TTAGTGAATAAACAG	8925
rs568377485	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63762691	AGACAATTCATTAAA[C/T]TGAAAACTGGTAAAT	8925
rs568379258	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63734140	CCACCCTACTCCAGC[A/G]TGGATGACAGAGCAA	8925
rs568383309	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63635870	TGTGTAATATATTTT[G/T]ACTATATTTTCTGTT	8925
rs568400705	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63740895	ATTTTCTTGAAAGTA[G/T]CCTTTGAAGCACAAA	8925
rs568417231	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63749068	TAATTTCCTCTTGAT[A/T]TGCAGATATTTAATT	8925
rs568456523	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63791191	CCAGACACTCTGAGA[C/T]AGTTTTACTTAATAA	8925
rs568457517	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63689461	CAGTGGAAAGGGAGA[A/C]AGAATGCCAAGAGAG	8925
rs568481541	in-del	-/CTTG			intron-variant	HERC1	GRCh38.p7	15:63746595	GCCATGCCCTAGGTC[-/CTTG]CTTGCCCTCAGGAAC	8925
rs568511043	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63648349	TTAGACAAAATGTAG[A/G]CGTACAGTGGGGATT	8925
rs568521170	snp	A/C	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63697704	AGGTGATCCACCCAC[A/C]TTGGCCTCCCAAAGT	8925
rs568534246	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63817953	ATCTACCTATTCCCA[C/T]AATAGATTAATCCAG	8925
rs568552058	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63746397	GATATTTTTAAGTTT[C/T]CCCCAAATTTAACAT	8925
rs568552860	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63719911	TAGACATTCTAGAGG[A/G]GATAGTGAGTAAACT	8925
rs568558328	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63720485	AAAATTTTTAGCCTC[A/T]AATTAATTTTGGTTC	8925
rs568583666	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63765455	CGGGAAGTGGGAGAT[C/T]GGACATGCCTCATTA	8925
rs568595728	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63610624	GGAAAGGCTCTTTTA[C/T]AATCCTTCCTGCACG	8925
rs568600930	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63816496	GCCCTGCACAAATTA[C/T]TTTTGAAATTTCTGA	8925
rs568612508	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63663255	GCATAAAATAATTCT[A/G]AATATTTCGCCAGTT	8925
rs568621841	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63782261	TACCTGCCTTCAAAG[A/G]ACAGGTTGAGTCTCT	8925
rs568625644	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63805532	ACTTTCTGGGTATGA[C/T]GAAAAGAGACTATAT	8925
rs568642940	snp	A/G			synonymous-codon	HERC1	GRCh38.p7	15:63645037	TTCTGCACTAGTCAC[A/G]TTGGTCTGTGTAGTA	8925
rs568645565	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63636674	CGAGGATGACAGCAA[C/T]AGTTACAGTCATTAA	8925
rs568651350	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63818503	AGACATCTTAAATAC[A/G]AATATAAAAATATAA	8925
rs568657035	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63610010	GGTAAAAATAGCTAC[C/T]ACTGGAGAGACAGGA	8925
rs568664511	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63777973	GCTAGTTATACCAAC[A/G]CCATTTATTAAGTAA	8925
rs568673770	snp	A/G			missense	HERC1	GRCh38.p7	15:63692434	CATTTCTGAGATGCT[A/G]TATTTAGAAGCACTT	8925
rs568695041	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63824351	ATCCTGGCTAACACA[A/G]TGAAACCCCATCTCT	8925
rs568708771	snp	C/T	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63631732	GTTTAGTAGAGACGG[C/T]GTTTCGCCATGTTGG	8925
rs568719092	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63631160	ATTTTAAGTTTCTTA[C/T]ATTCTAAAATGAGAG	8925
rs568727070	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63639598	TGTTTATCCAAATGT[C/T]TGTATACATAAATCT	8925
rs568734443	snp	A/C			upstream-variant-2KB	HERC1	GRCh38.p7	15:63834447	TATCTCTCATCGCAG[A/C]GGCCCCGGCCCTCCG	8925
rs568734566	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63823866	TTAACAAAATGAAAA[C/T]GTAGCCTACGGATTT	8925
rs568756372	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63753428	TACAGGTACTATATG[C/T]GTATAATTTTTCATA	8925
rs568778307	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63737749	TTTTGAAATGTGAGA[A/C]CACAAAGGACAAGAA	8925
rs568782481	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63639151	TACAAAATTACAGAG[G/T]TGGGCCAAATGGGCT	8925
rs568805387	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63683943	TTATTTCAACCCAAG[G/T]GAGTTGTGCTCAGCT	8925
rs568826186	snp	A/G	0.000277258	0.0117708	missense	HERC1	GRCh38.p7	15:63645636	TCTTTGGCACATGTC[A/G]TAAGAATATGACCTG	8925
rs568827819	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63705178	TTTTTTTTGAGACAG[G/T]GTCTCACTGTTGTCA	8925
rs568891455	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63800747	TTGGTGTTCGTAATT[C/T]CCTTTGTGATAGGGG	8925
rs568898083	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63700009	TGTGAACACAAGAAC[G/T]AGAAAACTAACAGTA	8925
rs568901791	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63794494	GTACTAACCCTCTAA[C/T]CATGGCTCAGTCTTT	8925
rs568908354	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63617209	TGTTCCCCTTCCTGT[A/G]TCCATGTGTTCTCAT	8925
rs568930551	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63650201	TGAGGTCAGGAATTC[A/G]AGACCAGCCTAGTCA	8925
rs568940212	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63657849	TTTTTTCTATGTGGA[C/T]AAACCATCAGACCCT	8925
rs568951546	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63659013	CCATGTATCACATCT[A/G]CTGATTATAAGTGCT	8925
rs568964860	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63821854	AGGCAGTGGAATAAA[A/C]AACATATCCAAGGTT	8925
rs568993478	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63647752	TAAGTCAGACACAGA[A/G]AGGCAAATATTACAT	8925
rs568994278	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63814014	CAGTGAGCTGAGATC[A/G]CACCATTGCACTCCA	8925
rs569021107	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63759823	GGGAGAGGATAGGGT[C/T]ATCTTGGTCAGATAC	8925
rs569021763	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63729972	CAGAGGTTGCAGTGA[A/G]CCAAGATCACGCCAT	8925
rs569024572	snp	C/T	3.3168e-05	0.00407221	synonymous-codon	HERC1	GRCh38.p7	15:63680765	ACCTCTGTTTTCCTT[C/T]ACAATATAAAACTAA	8925
rs569027415	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63723136	ATATATTTGCGAGCA[C/T]TATGAGCTAACTACA	8925
rs569029733	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63780786	ACAGCTACTACATCA[A/C]CATCTGTAAAATTCA	8925
rs569057137	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63826422	TCAATACGTACTGTA[C/T]ATACCGTTCAAAATA	8925
rs569080456	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63814521	CTGGAGTGCAGTGAC[A/G]CAATAGCTCACCACA	8925
rs569102128	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63789146	CCCAGGCTGGAGTGC[A/G]GTGGTGCAATCTCGG	8925
rs569120018	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63618626	GATATTGATTCTTCC[C/T]ACCCATGAGCATGGA	8925
rs569125940	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63796489	CCATCATCGATCATT[C/G]CGGGGTGTAGACTGT	8925
rs569127721	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime	HERC1	GRCh38.p7	15:63833901	AGGCTGCGGCGGTCG[C/T]GTCCTTTATTTTTGC	8925
rs569136864	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63789829	AAATAAATAAATAAA[C/T]AAATAAATGTATTAT	8925
rs569139073	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63653430	TCTGGGTGAGACTCC[A/G]TTAAAAAAAAACTGT	8925
rs569161452	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63795627	CCTGGTGCCACAAAG[A/C]AATAGCACTTGAACA	8925
rs569173863	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63653003	CTATACTTATTTGAA[A/G]TATAGCTTTAAGGTA	8925
rs569225346	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63774640	TCATTAAAAACTGCA[C/T]TGACTTTTCCAAAAA	8925
rs569251252	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63801879	TCATATGCTAATGAA[C/T]CCAGTCAAAACTTCT	8925
rs569257675	snp	C/T	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63617772	CAGTGATGATGAGCA[C/T]TTTTTCATGTGTCTT	8925
rs569267893	snp	C/G			intron-variant, downstream-variant-500B	HERC1	GRCh38.p7	15:63669017	CAGATGATATTCTAG[C/G]CTGTAAGACAAGTCT	8925
rs569288513	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63716541	TAAAACTTTAAAAAA[C/T]CTTTAATTTTTTATC	8925
rs569288542	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63708758	ATCAAAGATATGAAC[A/G]GTAATCTTAAATAAC	8925
rs569298123	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63807451	TTGCTCCAGCTCTCA[A/T]CAGTTTCCAGTGTTC	8925
rs569309606	in-del	-/CAAAA	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63649350	AGCGAGACTCCTTCT[-/CAAAA]CAAAACAAAACAAAA	8925
rs569316030	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63617007	TCTAAAATCATTATC[-/T]TTTTTTTTTTTTATT	8925
rs569316280	snp	C/G	1.78761e-05	0.00298961	missense	HERC1	GRCh38.p7	15:63696251	GACTGGAAGCCTGAA[C/G]TCAATCTGCTTCCTG	8925
rs569319361	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63721474	GAGGTTGCAGTGAGC[C/T]GGGATCACGCCACTG	8925
rs569325268	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63716027	CCCTATCTGATGACT[C/G]ATGAGTTTCATTTCA	8925
rs569342553	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63647481	AACTACCATTTGATC[C/T]AGCAATCCCACTACT	8925
rs569343258	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63688827	TTCCCAGGAATTTGC[A/G]TTTGGGAAACTAGGT	8925
rs569348896	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63672755	TTCAAAAATAACAGC[A/G]GGAATAAAAAACTTC	8925
rs569355466	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63661560	AAACTCCAGGGAAGG[A/C]TATGTTGCTATGCCA	8925
rs569390382	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63745638	CTGCAGGGGGAGGAG[C/T]GGCACTGCCTATTCA	8925
rs569405500	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63802565	GTTTTGTTTATTAAT[A/T]TAAGGTAAAAATTTA	8925
rs569424152	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63770110	CCCTGCCTAGCTTGC[A/C]GCCTCAATCTCATCT	8925
rs569436797	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63695540	TACAGGCGCCCACCA[C/G]CACGCCCAGCTAATT	8925
rs569455263	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63787599	TCAAGAATGACTTTG[A/G]TGGGTCAAACTATTA	8925
rs569465516	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63647151	CCCAGCTACTCAGGA[G/T]ACTGAGGCAGAAGAA	8925
rs569466759	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63793022	TATAATAAAGGCTAT[G/T]ACAAAGGGTATCAAT	8925
rs569474603	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63752775	TCTGGGTCACATATG[C/G]CAGGTTAGAAAACCT	8925
rs569495206	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63799321	GCCTGGGAAATATGG[C/G]AAAACCCTGTCTCTC	8925
rs569507819	in-del	-/TGTA	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63703398	GAGCAGCTGAAAATG[-/TGTA]TGTATACACCCATTG	8925
rs569519359	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63752246	TTGTCAATTAGTCAT[A/G]AAACACTTTTATACC	8925
rs569532118	snp	A/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63811334	AGTCTCACTTAAAGC[A/T]AAATGTATGCATGTT	8925
rs569534900	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63793124	TGCCACCCTCCAGGA[A/G]CTGCCAGAGGCGTCT	8925
rs569535012	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63804307	AAAAGTATTGCTAGC[C/T]GGGCACAGTGGCTCA	8925
rs569541167	snp	G/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63656595	AATTGAACTGACAAA[G/T]TAAAACAGGAATGTT	8925
rs569555205	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63751748	GCATATATATTTGAT[G/T]TCATATAACTTAAGG	8925
rs569556500	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63804623	GAAAATGAAAAGACT[C/T]AGATATGATGAACAC	8925
rs569559535	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63614268	AGAGCCTGGTTTGGG[G/T]TCTTGGCTCTGCTGT	8925
rs569572985	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63621441	ATTTTTTCCTTCATT[G/T]CAACTTTGGTGAATC	8925
rs569594830	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63621823	ACGTAGTTTTCGTGC[C/T]ACGGTTTTCAGCTCC	8925
rs569620212	snp	C/T	3.31214e-05	0.00406935	synonymous-codon	HERC1	GRCh38.p7	15:63612410	CTGATGCTGCTCATC[C/T]ACCTCACGGTACCGC	8925
rs569621193	snp	A/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63662316	AAAATGAGGCTTTTT[A/T]AAAAAAAAACTCCAC	8925
rs569657578	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63628897	TTTTTCTTAGATGGT[A/G]GCAGACATAAATAAG	8925
rs569665055	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63685616	GTAACTGGCTAAGTC[G/T]AGGACCCCTAAAAGG	8925
rs569684658	snp	G/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63719717	CACATGCATTTTGAA[G/T]GCAGAATTGACAGAA	8925
rs569685018	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63818944	AGTGCTGCCATTAGA[A/T]TTATAGTTTTAATCT	8925
rs569686472	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63727166	CTGTAATCCCAGCTA[C/T]TCAGGAGGTTGAGCC	8925
rs569687613	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63628321	TTTGAACCTGGGAGG[C/T]GGAGGCTGCAGTGAG	8925
rs569702597	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63777753	AGAGTATCCCTGCCC[A/G]ACTCTCACACCCAGA	8925
rs569708484	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63676583	GTAACATGGTGAAAC[C/T]CTGTCTCTACAAAAA	8925
rs569720858	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63719097	AAATCCCTGATCTAA[C/T]AGAGCTTATATTATT	8925
rs569721911	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63819592	TGTTCTCTTCTAACA[A/T]CTATTCCTCTCCTTG	8925
rs569777635	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63810655	TAAAAAAAGGGCAAA[C/G]ATAGTTTTCTATGGA	8925
rs569788184	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63778535	ACTGAGTGGTGAAGG[A/G]TAAAAGAAGAAAAAG	8925
rs569791813	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63748098	GGGCATGGTGGTATA[C/T]GCCTGTAGTCCCAGT	8925
rs569794317	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63830928	TGCTCTTTTTCACTT[G/T]TTGTAGTTAAAGAAA	8925
rs569801972	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63685171	CAAAACACCTCGAGA[C/T]GTCATCCACACTCTT	8925
rs569808264	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63699076	ATAAGGCTGAGTGCT[A/G]CTACCATAACCAACT	8925
rs569811878	in-del	-/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63805392	GCCAGACACAAAGAC[-/T]TACATAACTATGGTT	8925
rs569812949	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63817911	AAGATAAGAAAAAAT[A/G]CTGTATGGGAATTGA	8925
rs569822692	snp	G/T	5.27867e-05	0.00513717	synonymous-codon	HERC1	GRCh38.p7	15:63649801	AATCAGTCCCAGAGA[G/T]CCATCCATCCGTCCC	8925
rs569829634	snp	A/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63747473	TTAAAAAAAAAAAAA[A/T]TTTGTCAAGTCATGA	8925
rs569834020	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63755636	AATATGAAAATTAGC[C/T]AGGCATGGTGGCGCA	8925
rs569856329	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63643630	ATTCACTCTTGGAAA[C/T]TTTATATTTCAGAAT	8925
rs569862014	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HERC1	GRCh38.p7	15:63669361	TCTCTCCGAAATGGC[C/T]ATAATTCAATCCACA	8925
rs569881692	in-del	-/A	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63753585	AACCACACCAGGAAT[-/A]AAAAAAAAGTATAAA	8925
rs569896015	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63813469	AATCTAGGATAGTGC[A/G]AAAGGGTTTTTTTTT	8925
rs569900214	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63705741	TTAAATAAAAAATAC[A/G]TTAGGGTAGGCATGG	8925
rs569907590	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63741397	TGGTGTGATCTCAGC[A/T]CACTGCAACCTCCGC	8925
rs569929855	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63750005	AACAGCTGATCTGAA[A/C]ATAAAAATAACTGGT	8925
rs569930474	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63713815	TACAACATAGTTAAC[C/T]TAGTTAAAATTACAT	8925
rs569947165	snp	A/C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63779051	AGAATGAATTATAAA[A/C/T]GTGTTCAAGGAAGAG	8925
rs569954831	snp	C/T	3.31923e-05	0.0040737	synonymous-codon	HERC1	GRCh38.p7	15:63756464	AGGTCCCTGAATAAG[C/T]TTGGGATATTTCTGT	8925
rs569977411	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63805291	AATGGTTATTCATTA[A/C]AAGCAAAATGAATAA	8925
rs570011952	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63786179	AAGTGGGAGGACTGC[C/T]GGAGGCCAGGAGTTC	8925
rs570012764	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63615423	AGACCAGCCTGGCTA[A/T]CATGGCAAAACCCCA	8925
rs570050768	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63831396	ACAGGCGTGAGCTAC[G/T]GTAATCTGGCCAAAA	8925
rs570063906	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63638282	TGAAAGCTATATATC[A/G]TGACTTTCTTTAATG	8925
rs570066242	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63779527	ACTCTTAGTACAAGA[C/T]GGATCAAGTGAACAA	8925
rs570067672	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63821928	TAACCAGGTAGGCAA[C/G]TAATTCTATTTCAGG	8925
rs570076121	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63637843	TAACCAAGAGATGTA[C/T]GAGATTCATCCATTT	8925
rs570083535	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63825247	GAGGTTACAGTGAAC[A/G]CAGATCATGCCATTG	8925
rs570086344	snp	A/C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63795507	CTTGATTTTATTTTC[A/C/T]ATCAAATAGAAAAGC	8925
rs570093844	snp	A/G	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63736069	CCTCCCCAGAATGGA[A/G]AGGAAAAAACAGCAT	8925
rs570109492	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63724082	ACAAAATAAAATTTT[A/G]ATAGTTTCATGATTT	8925
rs570130334	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63773039	TTTCTACTTGTTGCG[C/G]GTAGGGGGAGACTTG	8925
rs570133266	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63806163	TCTGCAGAACACAAG[C/T]GGTTTTTTTTTTTTC	8925
rs570149143	in-del	-/GA	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63767762	ATGTCAATCACTTTG[-/GA]GAGTTCTCCGAAGAG	8925
rs570166209	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63741941	CTAACTTTCCTCTTC[C/T]TTTTCAAGACTGTTT	8925
rs570173052	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63800177	GGGTATGGGGAAATA[G/T]TCTCTCCACTAATGC	8925
rs570192935	snp	G/T	1.67525e-05	0.00289413	missense	HERC1	GRCh38.p7	15:63616642	AAAACTTAAACTGCA[G/T]TAAGTGTTCATCGAG	8925
rs570202464	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63687811	GGCCTCTCTGAAGAT[A/G]TGATAACTGAGACCT	8925
rs570233026	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63791387	CATATATTACAAATA[C/T]GAGCTCTGTGTATAT	8925
rs570241528	snp	A/C	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63687304	CAGCAATTTGAGAGA[A/C]CGAAGCGGGCGGATC	8925
rs570247207	snp	A/C	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63827997	GACTGCTAATGGATA[A/C]ACAGTTTCTTTTGGG	8925
rs570247321	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63695488	CCTCCCGGGTTCAAG[A/C]GATTCTCCCTGCCTC	8925
rs570252596	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63622967	CCAATTACAAGATCA[C/T]ACTGAAAAGAGAATA	8925
rs570262799	snp	G/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63742041	CAGCAAGAATTTTGA[G/T]AGTGATTGCACTCAA	8925
rs570267322	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63670761	TTAAAAACCATATTA[C/G]AATGTCGTATCAGGC	8925
rs570278151	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63701243	TAATGACATTAATTC[A/C]TTAATTTTATGGGAG	8925
rs570284563	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63721483	GTGAGCTGGGATCAC[A/G]CCACTGCACTCCAGC	8925
rs570290206	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63622532	GAGATGGGGTTTCAC[C/T]ATGTTGGCCAGGCTG	8925
rs570298928	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63717916	CTTCATTTCCAATGG[C/T]AGACAACTCTAATCA	8925
rs570304258	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63664083	CACAGAGCAGTACAT[C/G]AGAAAAGCCAGGGCC	8925
rs570312741	snp	G/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63765708	TATCCCATCCTTTCA[G/T]ATCAAACCAATAAGA	8925
rs570335514	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63717486	TATAATTTTACGATC[A/G]TGTTATCAAGATTAC	8925
rs570343616	snp	A/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63678622	AGATGTTAGGAAAAT[A/T]TGAAAGATGAATATA	8925
rs570349393	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63732013	GTGGTGGTGGTGGTG[G/T]TGTTTTGAGATGGGG	8925
rs570373386	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63724823	GAAATTCTAAAGGCA[C/T]TTTAAGTGGCGAAGA	8925
rs570373565	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63716737	TATTCATATCTATAT[C/T]GCTATTCAGCTATAA	8925
rs570379206	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63681556	TTGGCTAGGACCTGG[C/G]AATTTGACTGGTAAA	8925
rs570405462	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63822261	GTCATGGCTAGGAAT[C/T]TGGCTGTTCTTTTAA	8925
rs570417481	snp	C/T			missense	HERC1	GRCh38.p7	15:63672521	TAAGAGGCATCACTC[C/T]CGGGGACTCGGATGC	8925
rs570426434	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63632406	GGAGCTCTGATGGTC[A/C]AGGCAGTATTTGTGG	8925
rs570429158	in-del	-/ATCTCTTCATGTAAGAGATAAAGC	0.0111196	0.0737302	intron-variant	HERC1	GRCh38.p7	15:63706265	TGTAAGAGATATAAT[-/ATCTCTTCATGTAAGAGATAAAGC]ATCTCTTACATGCTT	8925
rs570449404	snp	A/C/G			intron-variant	HERC1	GRCh38.p7	15:63759984	GGATAGTGGGGCCAA[A/C/G]GGAGTCAGAATTGCT	8925
rs570456462	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63731506	GAAAAATTTTTGGTC[A/G]TTAACAAATGGCTAT	8925
rs570461111	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63641251	TAATACAAACTTGGT[A/G]TTTGTTTCTTTATTT	8925
rs570475199	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63640602	GAGTGAGTTGTACAG[A/G]TAGTACCGAGGATTT	8925
rs570480002	in-del	-/AAAT	0.0729998	0.176553	intron-variant	HERC1	GRCh38.p7	15:63789802	GCGAGCCCTGTCTCA[-/AAAT]AAATAAATAAATAAA	8925
rs570485035	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63788961	AATGATGGCTCAACA[C/T]AGGCAAATCTATTAA	8925
rs570495242	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63738879	AATCTTACACTACCC[C/T]GTTTCTGATAAATAT	8925
rs570495368	in-del	-/C	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63648907	TGAATTACCCCACTT[-/C]CCCCAGACAACCAAC	8925
rs570513886	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63647011	TGTAATCCCAGCACT[C/T]TGGGAGGCTGAGGCA	8925
rs570553492	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63746275	CTTGTAATTTCTTTC[C/T]TTGATCCACTGATAA	8925
rs570558791	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63809763	ACTAAGAAATATCCT[A/G]TTCATTGCAGCCTTG	8925
rs570567462	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63745056	TGTCATCTGAGAGCT[C/G]GCATCTGGAACAGGG	8925
rs570586799	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63623960	ATCACATGATATCTT[C/G]CCATCAGTGAATGAA	8925
rs570594001	snp	A/C	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63809224	TTTAACCTCTTCATC[A/C]AAAAATAAACAAAAA	8925
rs570618648	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63633462	AAGGAGACGTGTACC[C/T]GTGTTAATTCAGTGG	8925
rs570625246	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63657273	AGGTTTTTTTTTTTT[C/T]TTTTTTGAGACAGGG	8925
rs570639216	snp	C/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63620206	GTGTCTTTGTTCTCG[C/T]TGGTTTCAAAGAACA	8925
rs570671172	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63682303	CTAGCTAAAGTTAGG[A/G]AAAAAGAGCAGCTCA	8925
rs570671554	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63761801	AATGGCATATTCTAA[G/T]TCTCATCCTTGTATC	8925
rs570689875	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63626242	AAGCATACAGAGAAG[G/T]TGAGATAATTACACA	8925
rs570709490	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63635856	TCTCTTATAATTACT[A/G]TGTAATATATTTTTA	8925
rs570728689	snp	C/T	1.65669e-05	0.00287805	missense	HERC1	GRCh38.p7	15:63775493	GGTACTACTTCCTTA[C/T]TGCTAACCAGTTTAG	8925
rs570742022	snp	A/G	0.0337553	0.125452	intron-variant	HERC1	GRCh38.p7	15:63673621	ATGTGAGGATACAAG[A/G]TAAAACAGAGCTTTT	8925
rs570764828	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63611647	ACAGGAAGAGGCAGT[A/G]TGATGATCCTTCTGC	8925
rs570782385	snp	A/G	0.000116028	0.00761579	missense	HERC1	GRCh38.p7	15:63654232	GTGCAGCAAGAGTGC[A/G]CACGAGTTGCTGAGC	8925
rs570788634	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63754071	CCCAGCTACTTGGGG[A/G]GCTGAGGCAGGAGGA	8925
rs570829028	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63723749	TCTTTGAGAAACAAG[A/G]AACCATTGAAAATGC	8925
rs570833042	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63697288	TTCATGACGACACTT[C/T]GGAAGAGCTGTTCAT	8925
rs570865770	snp	A/C	1.70694e-05	0.00292137	intron-variant	HERC1	GRCh38.p7	15:63749359	TTTTTAAACATAGGC[A/C]CTCTTACCTGTCCCT	8925
rs570869419	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63696445	AAATTCTGACATTTC[A/G]TATGAATCTATTCTA	8925
rs570878195	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63753709	AGTAGGAGTGACTAA[C/T]TAAAGTAGACATAGA	8925
rs570887263	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63653570	TCTGTGGGTGATTGG[C/T]TCCATGATTCCCTGC	8925
rs570891735	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63720865	GGTATTACTCTCCTA[C/T]GCCATTTTTAAAATA	8925
rs570901114	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63803480	AGGCTGGAGTGGCAG[C/T]GACACAATCATAATT	8925
rs570922239	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63660823	CGTTGTTGCTATTAA[A/G]TTCCCTTGAGTTTTT	8925
rs570930220	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63752765	CTAAGATTTATCTGG[G/T]TCACATATGCCAGGT	8925
rs570936658	snp	A/C			missense	HERC1	GRCh38.p7	15:63694054	CTTCTCCGAAAGAGG[A/C]CATATGTAGTACACC	8925
rs570959122	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63660276	AGTAAGCTGAGATCA[C/T]GCCACAGCACTACAG	8925
rs570959441	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63649990	AAAAAGGAACAGAAA[A/C]AAATACTACTTAATT	8925
rs570986507	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63733280	AGGAAGTACATAATT[A/G]TAAAAACTACCCAAT	8925
rs571001959	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63796481	TCTAACCTCCATCAT[C/T]GATCATTCCGGGGTG	8925
rs571034240	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63746140	CTGATTCGATATATA[-/T]TTTTTTTAATATAGA	8925
rs571037999	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63785236	CAAGACCAGCCTGAG[A/C]AACATAGCAAGACAT	8925
rs571054552	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63725727	AATAAAATTTTCCTT[A/G]GAAAAGTTACTAATT	8925
rs571075165	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63641855	GAAATAATAAAATTT[G/T]TGAACTACCTCTGAT	8925
rs571081988	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63783563	TTACTATGACATTGG[C/G]TTTATTGTGATTTAT	8925
rs571086266	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63639052	CACAGGTACAAGGTC[A/G]TGTGGAGGACCCCAC	8925
rs571093559	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63830215	TACTGTGAAGAATAC[C/T]GCTAAGGGTTCAAAG	8925
rs571109310	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63779826	GGAGACCATCCTTGC[C/T]AACATGGTGAAACCC	8925
rs571114875	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63791108	GGTTTGTCCTTTCCT[C/T]GGACATACAGAAATT	8925
rs571142250	snp	A/C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63816271	ATTCCAAGAGAGAAT[A/C/G]AAGTACACATTGTTT	8925
rs571147632	snp	C/T	1.65825e-05	0.00287941	intron-variant	HERC1	GRCh38.p7	15:63638681	ACATTGACTGAGAAC[C/T]ATCATACAGTTATCT	8925
rs571150023	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63690146	CACTCCAGGCTGGGC[A/G]ACAGAGCGAGACTCC	8925
rs571158943	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63697822	TTACAATTTTATCTC[C/T]TTCCTATAGCCTATT	8925
rs571173016	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63609534	CTCTGACTGGCAGGA[C/T]TGCTTGAGAGAATAC	8925
rs571177919	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63743378	GCGATTCTCCTGCCT[C/T]AGCCTCCCGAGTAGC	8925
rs571195057	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63710808	GTCCTAAGAAACAGC[C/T]AGTTAAGGCCCTAAA	8925
rs571195703	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63822952	GTCCTGCCATTTATT[A/C]ATACTAAGAGCAGAT	8925
rs571233497	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63699848	AGCTTTAAATAAATA[C/T]ATAAATGTCCAATTC	8925
rs571247842	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63800035	GCTACTGGGGAGGCT[A/G]AGGCAGGAGGATCCC	8925
rs571256594	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63739432	GAACTATTTATCTCA[A/G]GTGATCTACCCTCCT	8925
rs571268908	snp	G/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63657263	TTTTTGTCTTAGGTT[G/T]TTTTTTTTTTTTTTT	8925
rs571308275	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63678797	AATCTGGATACACAC[G/T]GCAAATAAGACACAG	8925
rs571336869	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63757600	CCATTTGTGGTGAAC[A/C]TAACGGTAAAGTCTG	8925
rs571347746	snp	C/T	0.000200914	0.0100208	intron-variant	HERC1	GRCh38.p7	15:63672702	ATCAATCTCTAGAAA[C/T]CAAAAAAAAGGTTAA	8925
rs571349980	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63664033	TAATGTAATGAGGGA[A/G]TCTGGTCCTTATCTA	8925
rs571362531	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63822738	AAGGAAACCAGATAA[A/G]AGACTATTATAATTA	8925
rs571368827	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63663516	GCTGGAGTGCAATGG[C/T]ACAATCCCAGCTCAC	8925
rs571374675	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63686285	TTTCAGTCTTTCTAC[A/G]CATTTATTATAAGAA	8925
rs571377985	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63773232	CAGATCACCTGAGGT[C/G]AGGAGTTCCAGACCA	8925
rs571394039	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63790300	AAGTACTTTTTAGGC[C/T]AGGCGCGGTGGCTCA	8925
rs571413845	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63799455	CCGTGAGCTATGATC[A/G]TGCCACTGCACTCTA	8925
rs571416791	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63729941	GAGGCAGGAGAATTG[C/T]TTGAACCCCAGGAGG	8925
rs571422031	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63826387	CATTACTGGTCCAAA[C/T]AACTACCATACCATG	8925
rs571451581	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63737029	TTAAAAAAAAAAGTA[C/G]ATAGAAACAAGAACA	8925
rs571455866	snp	C/T	0.00597247	0.0543191	intron-variant	HERC1	GRCh38.p7	15:63814056	AAGCGCAAAACTCCA[C/T]CTCAAAAAACAAAAA	8925
rs571498910	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63742884	AATTTTTACATCTAT[C/T]TTCATAATGGATACT	8925
rs571508715	in-del	-/CCA			intron-variant	HERC1	GRCh38.p7	15:63652801	GATTACAGGCACGTG[-/CCA]CCACAACTGGATAAT	8925
rs571517798	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63806744	TTCTGCCTTTGTTGT[C/T]GTAAGTTGGAACTCT	8925
rs571529523	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63650592	CTGGCTGTCTGTAAC[C/T]ATTAATAGGGCAAAA	8925
rs571530502	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63792944	CCGCACTCCTGGGGT[G/T]TGATTACTTTCTAGA	8925
rs571532018	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63647877	CCTAGAGTGTGGAAT[A/G]ATAGACAAGGGAGAC	8925
rs571535518	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63627589	TGAGGCAGGAGAATC[A/G]CTTGAACCCGGGAGG	8925
rs571541994	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63624885	CAAATTAAGTAATTC[C/T]AAATCCTACCATATA	8925
rs571543822	in-del	-/AA	0.00161649	0.0283836	intron-variant	HERC1	GRCh38.p7	15:63804994	ATACACTGCTGGTAG[-/AA]ATGTGACATGGGAAA	8925
rs571552557	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63631693	TTACAGGCGCCTGCC[A/G]CCACGCTCGGCTAAT	8925
rs571555769	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63691267	GGCCAGGAGTTCAAG[A/C]CCAGCCTGGCCAACA	8925
rs571561243	snp	A/C	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63693331	TCACTGCAATCTCCA[A/C]CTCCCGGGTTCAAGT	8925
rs571580623	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63825891	CCTCAGCCTCCCGAG[C/T]AGCTGGGATTACAGG	8925
rs571601996	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63692829	ATAAAGAATTATTGG[C/T]GACTAGAGAACAGAA	8925
rs571618069	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63624008	CAAGCACTGTGCTAG[G/T]CCCACTGTAACCACA	8925
rs571619962	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63807398	CACAAAGCCATTTCC[C/T]CTAGGGCTACAGGTC	8925
rs571653213	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63801226	TTTCCCGTGTTCTGT[A/G]AGCCATTCTAGCAAA	8925
rs571656374	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63765887	TTTTGAGACTGTTTC[A/G]CTCTTGTCACCCAGG	8925
rs571660915	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63766656	TTAAGTTTCGTAATA[C/T]ATTAAAGGTTAGGGG	8925
rs571677325	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63631069	CTGCAGCCTCAACCT[C/G]TCGGGTTTAAATGAT	8925
rs571680705	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63813710	TATGCCTGTGTTTCT[A/G]TATGTACCATTTTAC	8925
rs571690108	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63703526	ACTGAGACTAGTAAA[G/T]GCAAATGCTGTATGA	8925
rs571690581	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63715074	GGTTAAGAGAATGGT[C/T]ATTGGTGTTTGGGGC	8925
rs571733875	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63802290	TAAAAAAGAAAAAAC[A/T]TTTTCGTTGTTATTA	8925
rs571767241	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63788208	CCAGTACAAGTCAGA[A/C]TGATGATTTGGGGAA	8925
rs571782603	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63747451	GGCGACAGAGCAAGA[C/T]ACCATCTTAAAAAAA	8925
rs571804870	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63667405	ATGTGAAATAAACAC[A/G]GAAGATGAGATTAAA	8925
rs571820514	snp	C/T	1.65699e-05	0.00287831	synonymous-codon	HERC1	GRCh38.p7	15:63612365	CTCATTGGAGAACTC[C/T]TCCAGCGTGTGCCAG	8925
rs571826799	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63752093	CCATAGTGAGAAACA[C/T]GTAGAAGAGATATTC	8925
rs571846187	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63737648	GCCTCCAAAAGTGCT[A/G]GGATTACAGGCGTGA	8925
rs571850179	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63658199	ATCCCCATGATGGCA[A/T]CTGCAGGCTGACTTA	8925
rs571887592	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63611896	ATAAAAGCAACAAGG[A/C]GCAGAGGGCCAGGCG	8925
rs571890819	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63759802	TAGTTTGCTAGCACA[G/T]GAAATGGGAGAGGAT	8925
rs571918585	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63697611	AGGCATCCACCACCA[C/T]GCCCAGTTAATTTTT	8925
rs571948507	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63803230	AAAAACTAATAAAAA[C/G]AAAAAAGTACTTGTA	8925
rs571949527	snp	A/T	0.0566069	0.158427	intron-variant	HERC1	GRCh38.p7	15:63829594	ATATATATATATATA[A/T]AATATACTGATATAT	8925
rs571966699	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63710380	CAGAAACAGGTAATA[C/G]GGCACTTCAATTAAA	8925
rs571980665	in-del	-/T	0.00557542	0.0525036	intron-variant	HERC1	GRCh38.p7	15:63748262	TACATTAAAGCTGAA[-/T]TGAGTTCAACAAGAT	8925
rs571989896	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63751473	GACACATCACTGTAA[C/T]ACTGTCACTCAGTAA	8925
rs571995865	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63617691	TCCTGACTTCTTAAT[A/G]ATCGCCATTCTAATT	8925
rs572000050	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63610870	CTTGTGAAGAGTGGG[A/G]ATGGAGACAGAGGGA	8925
rs572002940	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63717620	GCATTTTGGGAGGCC[A/G]AGGTGGGTGGATCAC	8925
rs572038425	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63815895	TTCACATGGGGGCAA[A/G]AAGGAGAAGTGCCTA	8925
rs572075670	snp	C/G	0.0271762	0.113356	intron-variant	HERC1	GRCh38.p7	15:63619738	GAGAGTGTATGTGTC[C/G]AGGAATTTATCCATT	8925
rs572077208	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63761241	GACTAGTATTGAGCA[C/T]TAAATAAGTAATCAT	8925
rs572085409	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63660087	ACTCTGGGAGGCCGA[A/G]GCGACTGGATCACAT	8925
rs572086011	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63620971	GTCTGTGCCTTTTAA[G/T]TGGAGCATTTAGCCC	8925
rs572096979	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63721252	AATGGGGCCAGGCGC[C/T]GTGGCTCACACCTGT	8925
rs572106463	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63719411	GTGCATGCACAGAAT[G/T]GGTAGAAGACATCAG	8925
rs572114983	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63753223	ATGTTTCTGATAGCT[A/G]AGGATGTTAACAAAC	8925
rs572134061	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63790883	TGTTTTCAATTGTAA[C/T]ATAATCAAAAGTTAT	8925
rs572135031	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63619067	GAGGGCATCCCTCTC[G/T]TGTGCCAGTTTTCAA	8925
rs572140385	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63726705	GAGTCTGTCTACAAA[C/T]AAAACACCAGGGCCA	8925
rs572145278	in-del	-/C	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63620000	CTATCTCCTTCAGTT[-/C]TGCTCTGATCTTAGT	8925
rs572177492	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63726013	AGCAGACAGAGTCTC[A/G]TTCTGTCACTCAGGC	8925
rs572183705	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63830298	TGCATTGAGAAGGAC[A/G]CAACATCGCTTCTGT	8925
rs572187484	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63823275	ATGACACTCAATCTT[A/G]GGGAGGGGGCTTAGG	8925
rs572191061	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63740307	ATTGTATGAATATAC[A/G]AAATTTTGTTCATTT	8925
rs572195676	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63684646	AAATATGGAGGAGTC[A/G]GGAGGGCATTAATGA	8925
rs572198393	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63811432	TCTTCATTTTTTCTA[A/T]AAATCTGAGAAATTT	8925
rs572209072	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63689067	TTGAGATGAAGGCAA[A/G]GTAAAAGTGGCACCA	8925
rs572219179	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63719086	TGAACAAAACTAAAT[A/C]CCTGATCTAACAGAG	8925
rs572224593	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63823876	GAAAACGTAGCCTAC[A/G]GATTTGGAGAAAATA	8925
rs572232985	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63690493	AGATTTGGGTGAATC[A/G]TTTTGCAAATATGGA	8925
rs572261512	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63747225	AGCACTTTGGGAGGC[A/G]GAGGTGGGTGGATCA	8925
rs572267962	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63656471	AATAAAATGTAAGCT[C/G]CACTATCATTAGCCA	8925
rs572269467	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63835431	ATACTCAAAAACAAC[A/G]AGCAAAAGCTCCTCC	8925
rs572287514	snp	C/T	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63739711	GGGCATGGTGGTGTG[C/T]GCCTGCAGTCCCGGC	8925
rs572293080	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63783846	GCTGAAGCGGGCAGA[A/T]CTCGAGGTCAGGAGA	8925
rs572301633	in-del	-/ATT	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63772776	AGAACCCATGTCAAC[-/ATT]CCATATCCCAAACAA	8925
rs572318635	in-del	-/T/TT			intron-variant	HERC1	GRCh38.p7	15:63675903	TATACTGTATACATC[-/T/TT]TTTTTTTTTTTTTTT	8925
rs572319082	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63648420	AAGGGCTACCTACTT[C/T]ATAATCTTTCATTCT	8925
rs572331212	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63653521	TAAAATAGTGAGGCC[A/G]ATTTCTTTTCCTTTT	8925
rs572352720	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63746543	TACAGTTCTAGTAGA[C/T]GATCCAGTCCACTTA	8925
rs572356858	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63647941	TGAGAGATTACTTGA[C/T]GGGTACAATGTATGT	8925
rs572362250	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63709681	CATCCTCCTTTCTAT[A/G]TTTTCATTTCAGTTG	8925
rs572367274	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63621624	TCCCACTTTCAGGTA[C/T]ACCAATCAGATGTAG	8925
rs572367929	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63711565	ATGAGGAATCCTTTA[C/T]GGAAGCTTTTTTAAA	8925
rs572404412	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63771517	CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG	8925
rs572415589	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63818084	AAGCTCTCCTATATA[A/G]TAATTACTCTTATTT	8925
rs572427854	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63740426	GGACATATGTTTTCA[A/G]TGCTCTTGGGTACAG	8925
rs572434067	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63793135	AGGAACTGCCAGAGG[C/T]GTCTGAACCAGAGCA	8925
rs572443485	snp	A/C	1.67061e-05	0.00289011	intron-variant	HERC1	GRCh38.p7	15:63635933	TATATTTACAATGAA[A/C]GGCAAACTTATCCAT	8925
rs572484653	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63623437	TGTCTGTTACATAAA[C/T]GTACATATATGCCAT	8925
rs572511682	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63626739	TAAAAACACATAAAA[G/T]AATAAAAACAAGATA	8925
rs572519857	snp	A/C	0.00398564	0.0444627	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834532	GTTCATGTCTTTGCG[A/C]CTTATGGGACTGCCA	8925
rs572529210	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63776664	GAATACACAGGTTGC[A/G]CATTTGTTAAAACCT	8925
rs572540370	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	HERC1, FBXL22	GRCh38.p7	15:63608683	CAATTCAAATTAAAA[C/T]AAAATAAATATATGA	8925
rs572541796	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63730002	TTGCACTCCAGCCTG[C/G]GCGACAAGAGTGAAA	8925
rs572578600	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63826055	AGGTGTGAGCCACCA[C/T]GCCCGGCCAAATAAT	8925
rs572584043	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63642255	TTTTACTAGAATATT[A/G]AATTTGAAAGCCAAG	8925
rs572592601	snp	A/G	0.000637494	0.0178421	intron-variant	HERC1	GRCh38.p7	15:63655720	ATTAGAAGACTGTAT[A/G]TTTCAGTAGTATGAA	8925
rs572616043	snp	C/T	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63826660	AGCTACATGTATGAA[C/T]GCAGTATTAGTGGAC	8925
rs572624819	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63712528	GTAACCCAACTCATT[C/T]GGGTGGAATGTCCAT	8925
rs572639740	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63662715	TGTAATTTATCTTTG[A/C]CATCAGAATCAAATA	8925
rs572641321	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63810824	TTAAGCAATCAAATT[C/T]AGCATTACCTATAAA	8925
rs572643037	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63804829	AGCCAAAAAAGCGCA[C/T]GAAAGGATGTTCAAC	8925
rs572661533	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63698287	GCCAAGCATGGTGGC[A/G]CATGCCTATAATCTC	8925
rs572706937	snp	A/G	5.01341e-05	0.00500645	intron-variant	HERC1	GRCh38.p7	15:63764060	ATAGCATTTTAACAC[A/G]AAGTTGTTAATACAA	8925
rs572729063	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63825911	GGGATTACAGGCACC[C/T]GCCACCATGCTCAGT	8925
rs572741157	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63772950	ATGCAAAAAGTAGGT[G/T]AAAACTTAAATGTCC	8925
rs572744527	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63751157	ATTCGGTCAATAGCA[A/G]ACCACATTATACAAC	8925
rs572807794	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63759230	AAATGGTGCTATTAA[C/T]ACATCACCAGTAAGG	8925
rs572825085	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63737319	AAAGAACACAGAAAA[C/T]AATGAAGAAGAAATC	8925
rs572848121	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63671782	TACACAGTGAAAATC[A/G]TAATGCCTTCTTAAC	8925
rs572849236	snp	A/G	4.9788e-05	0.00498914	intron-variant	HERC1	GRCh38.p7	15:63638795	AAAAACAGGGGGTAC[A/G]TAATGATCAATTCTG	8925
rs572866040	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63820019	AAAATGATGACTAAA[C/T]GAAGTAATGTATATG	8925
rs572905029	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63645291	CCCAGAGATAAGGAG[A/G]TTACATACCAAGTTT	8925
rs572905221	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63736694	GCTCACGGCAACCTC[C/G]ACCTCTGGGGTTCAA	8925
rs572927415	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63787603	GAATGACTTTGATGG[A/G]TCAAACTATTATAGA	8925
rs572937435	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63686013	TAAAAATTGTGGGCA[C/G]TGAATCTCTAATGGG	8925
rs572949094	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63646629	GCATGGTGAAACCCC[A/G]TCTCTAGTAAAAATA	8925
rs572953734	snp	A/C	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63658475	CTCACCCTCCCAAAC[A/C]CCACCAGACTTCCAG	8925
rs572966036	snp	C/T	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63613013	TTTTGAAAATAATTA[C/T]ATCCTTTTTGTAAAA	8925
rs572973000	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63716125	CCCAAAAGCATCAGA[A/T]TAGTACTAGCACAGT	8925
rs572981096	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63751627	CTGAAAGTGCTGAGA[C/T]AGACTGAGGGAAAAG	8925
rs572986703	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63813172	GCAAATTATTAGATA[C/T]TGTCAATAAATCAGG	8925
rs572988746	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63652585	AATTTTCTATTCAAA[C/T]GATTTTATTATTTGA	8925
rs572999458	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63617470	GCCGCAATAAACATA[C/T]GTGTGCATGTGTCCT	8925
rs573013733	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63708166	CTCCTCAAGGCATCA[C/T]TGTGTCAGGCAATAA	8925
rs573022698	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63788324	TTATTTACTGTAAAT[C/T]GGAGAATTGGGATAA	8925
rs573039409	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63807490	TTCCCCTCAGACTTA[A/G]AAGTGTACTAATGGC	8925
rs573047653	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63800959	GAAAAGGGGTGGAGA[C/T]AGAGTTAATCACCAA	8925
rs573050687	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63715451	ATTATTTTCCTTCCC[C/T]ATCTCCAACTCCCTT	8925
rs573056082	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63673756	TTGAGACAGAGTCTC[A/G]CTCAGCCGCCCAGGC	8925
rs573057123	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63769147	CACAGGCCGGGCACA[A/G]TGGTTCACGCCTGTA	8925
rs573058873	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63766202	CATAGAGGTCAAACA[A/T]TAACTTCATCAATAT	8925
rs573059042	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63739878	TGGACTTACACAATA[A/G]GCCCTTTGTGTCTGG	8925
rs573065416	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63614845	AAATGCATTCTTCAT[G/T]CAATTTCTTGCAAGT	8925
rs573082056	snp	C/G	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63814655	TGTATTTTTAGTAGA[C/G]ACAGGGTTTTGCCAT	8925
rs573083224	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63813891	TGGTGAAACCCCGTC[C/T]CTACAAAAAATGCAA	8925
rs573084646	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63801615	TAGGTAAAGCACATA[C/G]AGGGAGCTCAATAAA	8925
rs573085784	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63815163	TAGCCAACTCTCCAC[A/C]TTCGTCTCTTATGGC	8925
rs573098979	snp	C/T	1.65649e-05	0.00287788	missense	HERC1	GRCh38.p7	15:63775077	GACTGAGACCAGGTC[C/T]TGACACAGGCATCAT	8925
rs573143020	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63795728	CCACGAGAGTACACC[A/G]AACAAAAGAGACAGG	8925
rs573178581	snp	A/G	0.029116	0.117091	intron-variant	HERC1	GRCh38.p7	15:63789184	CAAGCTCCGCCTCCC[A/G]GGTTCACGCCATTCT	8925
rs573178935	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63832826	GTCCCAAGCAAGGAT[-/A]AAAAAAAAATGTGTC	8925
rs573202807	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63745211	CTGTGTAGCCTGGCA[C/T]TGGGGTCGGGGAGGC	8925
rs573207963	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63672368	ATGAGCTTGACTATA[C/T]AATCTCTTAGTTTCT	8925
rs573210617	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63647184	GCTTGAACCTGGGGG[C/T]TGGAAATTGCAGTGA	8925
rs573219468	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63809190	ATAGTATCAACCACT[A/G]ACTGGCTTCAAAGTT	8925
rs573246889	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63822812	GATGACAAAATGTGA[C/T]CAGATTAGAAATGTA	8925
rs573247040	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63637094	CAAAGGTGTTCTCTC[C/T]CCAAGTCACAAAGAA	8925
rs573312662	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63822493	CGGGAGGCTGAGGCA[A/G]GATAATCGCTTGAAC	8925
rs573314169	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834859	ATCAATTAAACTGAC[C/T]GATGACTTGGGGACA	8925
rs573343309	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63780615	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	8925
rs573347933	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63649130	GAGGCCAAGGTGGGC[A/G]GATCACAAGGTGAGG	8925
rs573380157	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63755155	GGCCTAGTAAATCTG[C/T]TCTCACGGCTTCTCA	8925
rs573384399	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63655447	GTCCCTTCAAAGTGT[C/T]ATAATCTTAAAACAA	8925
rs573385290	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63717035	CATCTAGACAAAGAA[A/G]AGAATCCTTAAAACA	8925
rs573417910	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63767585	CACCTGTAGTCCCAG[A/C]CACTGGGGAGGCTGG	8925
rs573421334	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63654775	TCGGGAGGCTGAGGC[A/G]GGAGAATTGCTTCAA	8925
rs573436359	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63632033	TTCTGGAGTTCCAGA[C/T]CTAAATTCTCAATAG	8925
rs573451288	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63681859	CAGGGAGAGAACAGA[A/C]GGAAGCCTACAGGAT	8925
rs573452358	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63626447	TTAACAATAGAACTT[A/C]GGCAGTTCTTTCACA	8925
rs573468849	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63724998	ATAACCTCCAAGCCT[C/T]GGAAAATAAGTGATG	8925
rs573474055	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63677089	TCCCAAATCTGAAAT[A/G]CTCCAATGGGCAACT	8925
rs573499121	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63822061	AAGTCTGAGGCACTC[C/T]CTTTAAACAGAAGCC	8925
rs573508848	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63684825	TCAGCCTGGCCAACA[C/T]GGCAAAACCCTATCT	8925
rs573512203	snp	A/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63681210	TTTGTTTTGTTTTTA[A/T]TTTTCTAAAGAGATG	8925
rs573526824	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63779096	TAAAGAAAAATGAAA[A/G]GGGTGAGAGAAATAA	8925
rs573532612	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63747580	AAGTTTAGCTCTTTT[C/T]TAGATTATAAAAAAG	8925
rs573539571	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63690872	ATAATGGGAAGAGCA[C/T]TGTAAAAAAGTATCT	8925
rs573551695	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63785454	ATAATTCAATTCAAA[A/C]TTAGAAAAACAAAAT	8925
rs573556373	snp	A/C			missense	HERC1	GRCh38.p7	15:63758240	CCTGTGTACCTTCTA[A/C]CAACTGATGGCTGCT	8925
rs573558548	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63828267	GGCATGGGCAAGAGG[C/T]AGAAACAAAGATGGA	8925
rs573562190	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63698612	AAAAGCTCAGGTACA[A/G]GAAAGGGGAAGGCAA	8925
rs573574118	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63698194	GCCGAGGCAAGTGGA[A/T]CACCTGAGGTCAGAA	8925
rs573594919	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63792444	TACTGACTTTTCAAA[A/T]CCCTTTCCAGATACA	8925
rs573647467	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63796569	TGCCAAGGTTAAGGA[C/T]ATGCCTGTGATACAG	8925
rs573648232	in-del	-/TTT/TTTTTTTT/TTTTTTTTTTTTTTT/TTTTTTTTTTTTTTTTTT	0.438806	0.163867	intron-variant	HERC1	GRCh38.p7	15:63720103	GTGCTTTTTCTTCCC[lengthTooLong]TTTTTTTTTTTTTTT	8925
rs573654228	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63622198	CAGAAAATTCATTAT[A/G]GGGAGGCCATGTGGG	8925
rs573688897	in-del	-/ACAG			intron-variant	HERC1	GRCh38.p7	15:63699773	AAATCTTTACATTAG[-/ACAG]CAAAATGTTAACATG	8925
rs573698088	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63806254	CAGTCATAGCTCAGT[A/G]CACCCTCAAGCTCCT	8925
rs573700001	snp	C/G	0.000399281	0.0141238	missense	HERC1	GRCh38.p7	15:63661765	TACCTTTCAGAACTT[C/G]TTGACTTAGATTTGG	8925
rs573702582	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63761739	TATTTTAGGACTGCT[A/G]TTTATGTGTCTATGT	8925
rs573715661	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63651162	TGTGAATTTCAAGGT[A/G]AAGAGAAACCACTGT	8925
rs573721321	snp	A/T			upstream-variant-2KB	HERC1	GRCh38.p7	15:63834848	TTCTAACGAGCATCA[A/T]TTAAACTGACCGATG	8925
rs573721781	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63830409	AAAAATAACAGTACT[C/T]ATCAAAAATGTCAAG	8925
rs573744485	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63778327	TCCACACCGTATCTG[A/G]AAACACTGGAAAAGT	8925
rs573750643	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63720176	TGGTGGCTACATAGC[C/T]CACTGCAGTCTCAAA	8925
rs573775350	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63735312	GCTCATGGAAGATAT[C/T]CCTGAGGATCAGGCA	8925
rs573792165	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63625461	ACTTTGGGAGGTGGA[C/G]GTGGGGGGGATCATT	8925
rs573822179	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63812296	TCTTCAACCCACATT[C/T]CCATTGTTTCAAAAC	8925
rs573838288	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63692056	TTATGATAAGAGAGA[C/T]TGTACAAATTCAGAT	8925
rs573859423	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63629254	CACGCCCAGCCCCCA[A/G]TAATAAAATACATTC	8925
rs573860345	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63643120	TAATTTACATTTAAA[G/T]TTCTATTTCACATTG	8925
rs573866326	snp	A/T	0.00517822	0.0506191	intron-variant	HERC1	GRCh38.p7	15:63824599	CTCTTCTCGGTTTTA[A/T]CCCAAAAGAAATAAA	8925
rs573877887	snp	A/C	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63728296	ATATTTTTTAAACAA[A/C]ATTTGCTTTTTTAAA	8925
rs573884054	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63771088	CAGCTACTGGGGAGG[C/G]TGAGGCACGAGAATA	8925
rs573904390	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63700139	ATGTATTCCTAAGAT[A/G]AATAATGGTTTTAGT	8925
rs573914488	snp	G/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63829147	ATACAGGCAGGGTAC[G/T]GTGGCTCACGCATGG	8925
rs573915322	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63769422	GAGACTCTGTTTCCA[A/G]AAAAAACAGGGCTAA	8925
rs573923529	snp	G/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63691396	ACTTGAGCCTGGAAG[G/T]GAGAGGTTGCAGTGA	8925
rs573939889	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63663618	TGCCACCATACCCAG[C/T]TAACCGTTTTTTAAT	8925
rs573952592	snp	C/T	0.0107246	0.0724382	intron-variant	HERC1	GRCh38.p7	15:63788712	ACCTGAGGTCAGGAG[C/T]TCGAGACCGGCCTGA	8925
rs573958124	snp	A/G	0.000200527	0.0100112	intron-variant	HERC1	GRCh38.p7	15:63734677	TCCTTCTCAGTCCAA[A/G]TTTTTAGGATACTAC	8925
rs573962966	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63830986	TTGCAAACTTCTCTG[C/T]AAATGATTTGACCAA	8925
rs573964111	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63799621	ATGGGTAGTAGTGGA[A/G]ATCAGTTATTAAGGG	8925
rs573996014	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63733807	CAGTAAGCCATGATC[A/G]TGCCACTGCACTCCA	8925
rs573998261	snp	A/T	3.53288e-05	0.00420276	intron-variant	HERC1	GRCh38.p7	15:63732895	CTACCCCTTTATTCT[A/T]TTTTTACTACAATGA	8925
rs574024794	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63740806	GCTGTAAGAATTCTT[C/T]ATATATTCTAGAAAC	8925
rs574038926	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63699379	TTAAGACACTGCTAG[C/T]AAGACCTACTCAAAA	8925
rs574045233	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63759742	AGTTTTTTGGTTTTG[A/C]TGAATCAAGCAAAAC	8925
rs574046273	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63771606	CTGGCTAATTTTTTT[A/G]TTTTTAATAGAGACA	8925
rs574049482	snp	C/T	3.80366e-05	0.00436083	intron-variant	HERC1	GRCh38.p7	15:63662966	AGTCAGAGCAGCCCC[C/T]GCTGCAGTCACACAC	8925
rs574050553	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63794333	GGTCTGGATCAGAAC[C/T]CCTTTCCTGTAACAC	8925
rs574082456	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63670221	AAAACAGTACATGAA[C/T]GATATGTCAGCGGCA	8925
rs574085711	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63622624	AGGCGTAAGCCACCA[C/T]GCCTGGCCTGTTTCC	8925
rs574085871	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63709626	TTCTGAGTCAGATTT[C/T]ATAGCTGATTTCCCA	8925
rs574106203	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63809463	ATAAAGATACATAAG[C/T]AATTACAGTACAATA	8925
rs574112081	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63676993	TGCACAGGATCAGAA[C/G]TGTTCTGGATTTCAG	8925
rs574123697	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63757140	TATTTGAAAAAAAAA[A/T]ACATTTTAATGAAAG	8925
rs574148254	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63622134	GTAATTGCAAATACT[A/G]AATTTTGTGACTTGC	8925
rs574150491	snp	A/C/T	5.12571e-05	0.0050622	missense	HERC1	GRCh38.p7	15:63764190	CGATCAGCAGATGAA[A/C/T]CCTATAATTAAAACA	8925
rs574157179	snp	G/T	1.74683e-05	0.00295531	intron-variant	HERC1	GRCh38.p7	15:63692396	TACTCTAAGACAAAG[G/T]CAAAGGACATGTACC	8925
rs574163669	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63793763	TTTCCAGTACAGAAC[C/T]TCTATGGGTTCAGCT	8925
rs574175049	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63721521	ATAAGAGGAGACTCT[A/G]TCTCAAAAAACAAAA	8925
rs574192977	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63814721	TTATCTGCCCGCCTC[A/G]GCCTCCCAAAGTGCT	8925
rs574199807	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63644698	GCTCCCATGGAGTTT[A/C]TATTTTAATGTACTA	8925
rs574235709	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63742300	TGTACATTGTTGGTG[C/T]ATAGAAACAATTTTT	8925
rs574236690	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63719842	GGAAGACCACATGAA[C/G]AGTTTCGAGGGTAGG	8925
rs574237837	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63657448	GAGATCCTCTTTTGT[C/G]AAACACTTCTTAATG	8925
rs574272118	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63680849	CTGCATTAACCAATA[A/C]TGAAAATATGTTTAT	8925
rs574299067	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63787057	ATGTTGGCCAGGCTG[A/G]TCTTGAAGTCCTGAC	8925
rs574301916	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63793338	CAAAACCAAGATGGC[A/C]ACGAAAGTGGCCTCT	8925
rs574331999	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63650834	AAATGAAAATACTAA[C/T]AAGCTCGATATTACA	8925
rs574347334	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63702907	TCAGGAGTTCAAGAC[A/C]AGCCTGGCCAACATG	8925
rs574348371	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63618894	CTTAAGGAGATTTTG[C/G]GATGAGATGATGGGG	8925
rs574348984	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63710256	AGCACAATCAGCAGG[G/T]AGGTGTTTTGTTGTT	8925
rs574366568	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63758020	GCAAAAATTTATTTT[G/T]CTATTAAAATGAAAA	8925
rs574375440	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63802204	ATTCAGCTGAATGAT[A/T]GATGTTGGTACTCTT	8925
rs574377887	snp	C/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63716909	TCTAAATTTAAAACA[C/G]TATTGGTTTTAATTT	8925
rs574381910	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63684488	TGTGTGAAAACTCTT[C/T]CTCTTGCATCCAACC	8925
rs574383169	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63618289	ATTTGTTTCTGTCAG[A/G]TTTGTCAAAGATCAG	8925
rs574401757	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63749866	AGGGATAAATGAAAT[A/C]TATGAAACTAAAGTG	8925
rs574413179	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63724283	GAATTATCTTTATCA[C/T]GTTAAAGACCCCTTG	8925
rs574418163	in-del	-/C	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63813870	GTCAGGAGTTTGAGA[-/C]CAGCCTGGTGAAACC	8925
rs574440129	snp	A/G	0.000184497	0.00960284	intron-variant	HERC1	GRCh38.p7	15:63716286	TGTATCTAGAAAGTA[A/G]GAAGGGTATACTCAC	8925
rs574443976	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63706611	GTCTTCGTTTTAACT[C/T]TTCTGATAAAATGAT	8925
rs574444110	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63625672	GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC	8925
rs574445390	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63822004	TGTAGGGAGTGGCCA[C/T]TATTTTACACTGTAT	8925
rs574472396	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63627213	ACTTTTCTCTCTTAG[A/T]TATCTAAGAAACAAA	8925
rs574504601	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63696098	ATGACAGTTAAAATC[G/T]GTATATACTGCAAGG	8925
rs574511963	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63673229	ATATATTTTTTTTAA[C/T]TGTTAAGGAATCCTA	8925
rs574524829	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63796558	AAAGTTTATTTTGCC[A/C]AGGTTAAGGACATGC	8925
rs574532453	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63664400	TAGTTTGAATCTTCT[C/T]TAATGTGCCTTTACA	8925
rs574538486	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63817441	ATCCAGAGGCCGGGT[A/G]TGGTCGCTCACACCT	8925
rs574554562	snp	A/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63632487	CTCTTCTAGCAAGAG[A/T]GCTGGCTCTGGCATA	8925
rs574564906	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63732254	GATCCACCCAACTCG[A/G]CCTCCCAAAGTGCTG	8925
rs574585320	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63767480	CAAGGCGGGTGGATC[A/T]TCTGAGGTCAGGAGT	8925
rs574587964	snp	A/C	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63731601	TTTAAATCTGAAAGA[A/C]AAGAATTTTGTAGGA	8925
rs574588680	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63656653	ACAAACCCATGTCAC[C/T]GCCCTCCAGATCAAG	8925
rs574592862	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63673581	ACGAATCTCATTTTT[A/G]TTTCTGCATTCATAT	8925
rs574594487	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63745879	GGGTCAGTAGTAATA[G/T]CTTGTCTTTCATTCC	8925
rs574595227	snp	A/C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63613335	CAGGCAAGTTGGGGA[A/C/G]TGCCAAGTAGGGTGC	8925
rs574605098	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63739612	GGGAGGTCGAGGCAG[C/G]CAGATCACCTGAGGT	8925
rs574610587	in-del	-/GTGC	0.000854609	0.0206537	intron-variant	HERC1	GRCh38.p7	15:63612589	GCTCATTCAATGAGT[-/GTGC]GTGCGTGAACCTGGC	8925
rs574653641	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63752582	CCTAAGTGTTCTCTT[C/T]ACCCTCCTTTTTGAT	8925
rs574657489	snp	A/C/T	0.000697957	0.0186686	intron-variant	HERC1	GRCh38.p7	15:63753089	GACCAAGTTTACCTA[A/C/T]AAAAACAAACACATT	8925
rs574675836	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63612743	CTCTCAACCCTTGTT[A/G]GAGTGCCTCCCTGCT	8925
rs574683622	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63803063	AAAAATAATTTGGCA[A/G]GCATAGTGGTGCACC	8925
rs574696006	snp	C/T	0.00438332	0.0466095	intron-variant	HERC1	GRCh38.p7	15:63823063	ATATAAGTAAACTCA[C/T]GTCATGGGGGTTTGT	8925
rs574697669	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63790345	GCACTTTAGGAGGCC[A/G]AGGCGGGCGGATCAC	8925
rs574698167	in-del	-/AAAAAATAAAAACC	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63709760	TCAGGGGCATTTAGG[-/AAAAAATAAAAACC]AAAAATAAAAACCAA	8925
rs574760051	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63761906	GAATTTGAAAGTATC[A/G]GTATGAACTCATTAG	8925
rs574761132	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63684735	ATGTTGGGCCAGGCG[C/T]GGTGGCTCACACCTG	8925
rs574771285	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63776554	AATACTTCAATCAAA[A/G]TAGTGGTTGCCTCTA	8925
rs574804860	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63660047	TGAGCAGCCAGATGC[A/G]ATGGCTCACGCCTGT	8925
rs574807960	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63642129	CATCATTTAACCATA[C/T]AAAATGTAAATCAAA	8925
rs574873639	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63783780	AAAGAATAAAACTCA[C/T]GATCGGGCCGGGTGC	8925
rs574876686	snp	A/C/G	3.31347e-05	0.00407019	missense	HERC1	GRCh38.p7	15:63638751	ATAATTTGTTCATCC[A/C/G]TGCCGTTAATCCATT	8925
rs574882000	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63688902	GGGGGAAGGGTTTGA[A/G]GGGGAGACACCCAGG	8925
rs574891465	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63822560	CACTGCACTCCAGCC[C/T]GGGCAACAGAGCAAG	8925
rs574892705	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63707179	TAAAGCCTTGAAGTA[C/G]TGCCTTATTTTCCAA	8925
rs574894997	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63662028	ACAAACATGCTGCAC[A/G]AAAGGATTTCATACC	8925
rs574895703	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63682671	CTATTTTCTTAAGCT[G/T]AGCTTTTGCTATTGC	8925
rs574930357	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63736591	CTTTTAGCATCCATC[A/G]GTCTTTTAGCATCAC	8925
rs574938541	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63638039	AGGGTTTGGCGCTAT[A/T]TCGTACCAGGATTAT	8925
rs574939646	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63803789	GCAAGGCAGGAAGGC[A/G]ATGGACTGAGAATAG	8925
rs574945645	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63804292	AACTTTTGTCCTTCA[A/G]AAAGTATTGCTAGCC	8925
rs574969612	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63735644	ATTATCTTAGGCCTC[A/G]TAACTTCTCTGGGTC	8925
rs574992447	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63718417	TAAGTAAATCTCAAA[C/T]CTTTTCCTTTTTTTT	8925
rs575000245	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63768831	CATTTAGAGCTGTTA[C/T]ATAATTAACTGAAAT	8925
rs575005396	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63719267	TGGGAAAGTTTCTGA[G/T]AAGGTTACATTTGAG	8925
rs575008825	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63742240	TATCCTATTCTTTTT[A/G]ATGCTTTTGTACATA	8925
rs575015492	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63728745	GAGGATAGAAGGCAA[A/C]ATTCGGAGGATCCTC	8925
rs575026654	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63668516	CAAACAAAGCAAGAC[C/T]TAACTACTACAACAT	8925
rs575043691	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63777479	TTGATAGCTGTACAG[A/G]GATACGTTGTTACTC	8925
rs575054231	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63664391	TAGTATCATTAGTTT[A/G]AATCTTCTTTAATGT	8925
rs575060355	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63810709	TGTAGGAGAGACAAC[A/T]TTCACGTGATCTCAA	8925
rs575078462	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63769649	ATCTGAGGTCAGGAG[C/T]TCGAGACCAGCCTGG	8925
rs575078672	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63711620	ACTTTATACTTTTTC[A/G]AAAATATTTTCCTAT	8925
rs575078828	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63704501	CTACTCAGTAAGTCT[A/G]GAGCCATTTTCTCTC	8925
rs575082440	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63631859	CCAAGTCTTATTCCT[G/T]TGCCCACCTGCCCTT	8925
rs575094927	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63829072	AAGGTTAGAATGAAC[C/T]TTGTGGTACTGGATT	8925
rs575132205	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63692903	CCCAAATATCAGGAC[A/T]GGCGCAATGGCTCAC	8925
rs575134814	snp	C/G	5.02206e-05	0.00501076	intron-variant	HERC1	GRCh38.p7	15:63758165	TTTGTAAGCTATTTA[C/G]AAAACTTACGGTCTG	8925
rs575135129	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63765964	TGTCTCAGACACTTC[C/T]TGGTTTACACTCATC	8925
rs575138442	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63825965	ACGGGGTTTCACCAT[A/G]TTGGCCAGGCTGGTC	8925
rs575174654	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63816637	CCTTTAAATAAAGTG[C/T]ATTTATTCAACATTC	8925
rs575181552	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63765456	GGGAAGTGGGAGATC[A/G]GACATGCCTCATTAT	8925
rs575185740	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63760082	TTCCAGGACAAAGCC[C/T]CTACACTGAGAAAAA	8925
rs575232207	snp	C/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63831775	ATCCAGTCCAATCAC[C/G]AACACATTCTCCAAA	8925
rs575244561	snp	C/T	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63646475	AATTTTAAAAGAAAC[C/T]AGTATCAAGCAATAG	8925
rs575253983	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63794908	CTATCTCTACTAAAA[A/G]TACAAAAATTAGCCA	8925
rs575266923	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63644631	TAATATAAATAAATC[A/G]TTCTTCATAGCAAGG	8925
rs575304494	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63650143	CACAGTGGCTCATGC[C/T]TGTAATCCTAGCACT	8925
rs575310003	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63758921	TTTTAAATAGATGGG[A/G]TCTCATTATCTTACA	8925
rs575316036	in-del	-/AA	0.00311803	0.0393611	intron-variant	HERC1	GRCh38.p7	15:63696935	ATCCTTCTTCTTTAA[-/AA]AAAAAAAAAAAAAAA	8925
rs575318119	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63658412	TAACAATGACTACGT[C/G]TAACATCTTTCATTC	8925
rs575321584	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63685389	CAGGTGCCCTAATAA[G/T]TATAAATTCTTTGTT	8925
rs575340926	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63624064	CTATCTACCCTGCCT[C/T]AGAAGTGAGGAAACC	8925
rs575365706	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63786474	ACTGGAGCATTACTC[A/G]TAATAGCCAAAAAGT	8925
rs575374676	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63722564	CTTTTAAATTGCATG[C/G]CCTTCTGAGTAGTAT	8925
rs575379816	in-del	-/TAACA			intron-variant	HERC1	GRCh38.p7	15:63815724	TCAAATCCTCTAACC[-/TAACA]TGTTAGTCCGGTCTC	8925
rs575403607	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63623195	GTAATGATAGCCAAC[C/G]ATTATTTTAGTCACA	8925
rs575403751	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63788519	TTCTTTTTAAGCAGT[C/T]AATAAAGTAACAATA	8925
rs575405753	in-del	-/A	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63721622	TTTCATTTTCTTTAT[-/A]AAAAAATAAAGGCCA	8925
rs575443017	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63687310	TTTGAGAGACCGAAG[C/T]GGGCGGATCACAAGG	8925
rs575452440	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63773300	AGTACAAAAATTAGC[C/T]GGGCATGCTAGTGCA	8925
rs575459854	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63692274	GTTTTCTTTTGATCA[A/T]ATAGGTACGCAGAAA	8925
rs575483875	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63813804	CAGGTATGGTGGCTC[A/G]CGCCTGTAATCCCAG	8925
rs575490950	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63671700	TGCCCAGGTGGCCTT[A/G]GGCACACCAAAAATT	8925
rs575493659	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63791000	TAACAACAAAAAATC[A/C]TAAAAAAGTTTTTCA	8925
rs575502478	in-del	-/C			intron-variant	HERC1	GRCh38.p7	15:63811829	AAAAAAAAAAAAAAA[-/C]AGAAAGGAAAAAACA	8925
rs575503781	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63715154	ATTTTGCATCCTTAA[A/G]CCTTAGTTCATTCAT	8925
rs575540554	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63714610	GCTGGAGTGCAGTGG[C/T]ACGATCTCGGCTCAC	8925
rs575600331	snp	C/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63751552	ATGAGAAATACTTGG[C/G]TTGCCTTTAGAGACT	8925
rs575610100	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63819944	CCCATAAGTTTAAAC[A/G]TGCGTTAAATAATAC	8925
rs575613366	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63797419	TAAGATTGGTTTTTT[C/T]GTGTTATCTTTCAGA	8925
rs575633117	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63786043	AAAAAATGAAAACAA[A/T]CAGCTAACAAAATTA	8925
rs575644150	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63797546	ATTTTTTTTTCCCTG[A/C]CCAATCAACATTCCC	8925
rs575644900	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63813289	CCTCCCACCACTACA[A/G]CAGTACTGATAATCA	8925
rs575671896	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63665170	TTTACACTTAAAGGG[A/G]CATCTTCTACTAGAT	8925
rs575705439	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63750910	CCACTGTACTCCAGC[C/T]TGAGCAAAAGAGTGA	8925
rs575734245	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63610931	TTCTGGGTTTGAGGG[C/T]TGTACCCAGTGTTCA	8925
rs575749170	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63660644	CTCCAGAAAAATCAA[C/T]GCTCATCTCTATTTA	8925
rs575762795	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63707904	ACTGCACTCCAGCCC[G/T]GATGACAGAGCAAGA	8925
rs575768403	in-del	-/TG			intron-variant	HERC1	GRCh38.p7	15:63758625	CTGCATACAAAACAC[-/TG]TAGAAAAACAAAGCT	8925
rs575803672	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63821686	GAGCCATGATCCCAC[C/T]ACTGCACTCCAGCCT	8925
rs575806963	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63684186	CTAGGTGATGTCCCA[A/C]CATGTTAAGCTTTCT	8925
rs575815748	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63612028	CGTCTCTACCAAAAT[A/G]TACAAAAAAATTAGC	8925
rs575862727	snp	A/C	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63754269	TACTTTGGTTTTTAA[A/C]AACACATCTAAGTAG	8925
rs575864425	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63711832	AGGCACTACCATCTT[C/T]GTATCACACAGTAAG	8925
rs575887367	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63791475	AACATAAGGGATGAT[C/T]TTTTTCAAAACAAGA	8925
rs575916455	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63827513	GATATACTATTGAGT[A/G]AAAAAAAGTGCAAAA	8925
rs575923770	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63697639	TTTGTATTTTTAGTA[G/T]AGATGGGGTTTCACC	8925
rs575945102	snp	A/C/T	6.20521e-05	0.00556976	synonymous-codon	HERC1	GRCh38.p7	15:63643488	GGCAACAGTCCGAAC[A/C/T]GGAGTGATGTGTCCC	8925
rs575949050	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63731165	ACTTAACCACTCCTC[C/T]ATTTTTAGATGTTTC	8925
rs575965635	in-del	-/CA			intron-variant	HERC1	GRCh38.p7	15:63813349	ACACACACACACACA[-/CA]AACTCGTAAGTACAC	8925
rs575968880	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63705023	GATTACAGGCATGAG[A/C]CACGACACCCCACCC	8925
rs575977795	snp	C/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63639461	ATACACTCTATGATA[C/T]TCCCAGCGTCAAGAT	8925
rs575980750	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63665812	TTTCATATAACTATA[C/T]TTATCAACTTTACAT	8925
rs575982282	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63741507	TAGTAGATACGGGGT[C/T]TCACCATGTTAGGCT	8925
rs575984723	snp	G/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63738281	GACTAAGGAATTGTT[G/T]CAGGACACTAAATTG	8925
rs575986740	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63738267	GAAAGACAAAGAAAG[A/G]CTAAGGAATTGTTGC	8925
rs575993426	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834232	GACCGCCTGCGGGGA[A/C]CTGACTCCACAGATG	8925
rs575998983	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63654731	AGCCACACCATGGTA[C/T]GGTGGCACGTGCCTA	8925
rs576016713	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63712625	ACATATGTGGTAAAC[A/G]TATATGCAATATAGT	8925
rs576041300	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63741090	CTGGAGTGCAATGGT[A/G]CGGTCTCCACTCACT	8925
rs576048779	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63735983	ATTAAGAACTAAATG[C/T]ACATATTCTGTTTCC	8925
rs576062049	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63753287	TGATAGCCTTTTATA[C/T]CTTAATTTCAAGCAA	8925
rs576066148	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63653990	TTTGTAATTGTGTGC[A/G]TGTGTATGTGTACGT	8925
rs576099631	snp	C/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63803700	CATTCCTCCTAACCA[C/G]TCTTTCAAGATTATT	8925
rs576105862	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63771496	AGTGCAATGGTGCGA[A/T]CTCAGCTCACTGCAA	8925
rs576122977	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63709301	AGGCATGAGCCACTG[C/T]GCCTGGCCCAATCTT	8925
rs576143449	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63744928	AGCTGGGTATCAATG[A/C]TGGTTATTCACAGCC	8925
rs576148899	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63784728	CTCTCCTGCCTCAGC[C/T]TCCCAAGTAACTGGG	8925
rs576155795	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63684727	AAAAATCTATGTTGG[C/G]CCAGGCGCGGTGGCT	8925
rs576158721	snp	A/G	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63711218	TAATCTCAGCTACTC[A/G]GGAGGCTGAGGCAGG	8925
rs576162061	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63818215	GTCACAGAAAAAAAA[C/T]TGCAGACAATATTGC	8925
rs576178765	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63741638	CAGTTATAGCTCTTA[C/T]ATTTAGGTCTTTAAT	8925
rs576186644	snp	A/C	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63609609	CACCTGTCCTTCATA[A/C]CCATCCACCAAGAGG	8925
rs576206689	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63743960	GATATTTTAAAGGAC[A/T]TGGGTATTATGATCT	8925
rs576240853	in-del	-/AAATAAAT	0.0456336	0.143994	intron-variant	HERC1	GRCh38.p7	15:63789802	GCGAGCCCTGTCTCA[-/AAATAAAT]AAATAAATAAATAAA	8925
rs576241027	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63783939	GGCATGGTAGTGGGC[A/G]CCTGTAATCCCAGCT	8925
rs576241234	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63613496	CTCAAAACCATCTAC[C/T]ACCATTTAAAAAGTC	8925
rs576248226	snp	A/G	0.000859173	0.0207087	synonymous-codon, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609261	GGTAGGCAGACTGTC[A/G]TAAGGCTGTGGAGAG	8925
rs576252314	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63616052	GGAACACAAAACAGG[C/T]AGGACTGATCAGGCT	8925
rs576269301	snp	A/C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63829738	GGAGAAGTAGTCGAC[A/C/T]CCAGGACTGGTGCAA	8925
rs576280658	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63713098	GAGCAATGCAAGTAA[C/T]TTCACATGCTTTTTC	8925
rs576288380	snp	A/C	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63636246	AACCACCGAATTGGT[A/C]CTATGAAAATAAGAA	8925
rs576298407	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63823527	GGGAAAGAACAGATC[G/T]AACTGGTGACAATGC	8925
rs576332522	snp	A/G	4.68143e-05	0.00483787	intron-variant	HERC1	GRCh38.p7	15:63643071	ATCCTAAAATGAGAT[A/G]TATTTACCAATACAC	8925
rs576338923	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63670136	AAATTATTCACATGG[A/G]TTGAAAGTAATGGTT	8925
rs576350656	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63635109	CTGGAGTGCAGTGGT[A/G]TGATCACAGCTCACT	8925
rs576366624	snp	A/G	0.00318978	0.0398085	intron-variant	HERC1	GRCh38.p7	15:63621685	TTGGAGGCTTTGTTC[A/G]TTTCTTTTTATTCTT	8925
rs576371289	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63642655	TGAGATAGTTTAGTG[C/T]TACTGTCAAAAATCA	8925
rs576381574	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63741017	TGATAAAGATTTACA[C/T]CTATGTTGTTTTTTT	8925
rs576383998	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63622064	TCTGTTTTTAATTTA[C/T]AAGTCCATGAAACAG	8925
rs576399484	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63718490	GCAATAACCAAGGCA[C/T]ATTTTTTTCTCACAT	8925
rs576405813	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63767781	GTTCTCCGAAGAGCT[C/G]AGTATTACATGGCAG	8925
rs576420751	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63716150	CACAGTTGTAGGAGC[A/C]CCTGTCAGCTAATAC	8925
rs576429661	snp	C/T	6.65104e-05	0.00576635	missense	HERC1	GRCh38.p7	15:63628713	GTGGTGCTGTCCATG[C/T]AGCACTGTGGCAGCG	8925
rs576451035	snp	A/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	HERC1, FBXL22	GRCh38.p7	15:63608474	AAGTGAAGCCCACCC[A/T]CAATGTAAAGAAATG	8925
rs576453584	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63722852	AGGTACGGTACTACC[G/T]GTGGTTTCAAGCAAT	8925
rs576457475	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63715633	CCAAAGGCATTGCTG[A/G]TCATGTTTTAGGGTA	8925
rs576457836	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63669516	CAACTTTGGATATCA[C/T]AGTGCATATCAGCAC	8925
rs576470903	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63676945	TACTTATCAAGGAAG[A/T]TACTTGACAGGATGA	8925
rs576476729	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63824487	TGCAGTGAGCTGAGA[C/T]CATGCCACTGTACTC	8925
rs576496045	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63722847	ATATAAGGTACGGTA[C/T]TACCTGTGGTTTCAA	8925
rs576502525	snp	G/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63770552	GTTATTTTTTATAAT[G/T]TGAAGATGTACACTG	8925
rs576526988	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63827401	TGCACTCCAGCCTGA[C/G]CAACAGAGTGAGACT	8925
rs576529549	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63651700	TATTTGCCTAAACTC[C/T]TGGGAATACTTCAGA	8925
rs576551710	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63654700	TCTACTGAAAATACA[-/A]AAAAAAAAAAAAATT	8925
rs576558653	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63799539	AAAAGAAAAATATTG[A/G]TCCTTTCTGCCAGTA	8925
rs576563179	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63821277	AATTAGCAGGGGGCC[A/G]GGTGCAGTGGCTCAC	8925
rs576578046	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63636826	TCACAAAGAGGTCTC[A/G]AAGCTTGTGCAATGT	8925
rs576611443	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63706229	AATTTGTTCCTCATG[A/G]AATTTTTAAAATATT	8925
rs576612417	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63763550	AATGGAGGAGGGAAC[C/T]TAGAGATTAAAATAT	8925
rs576615823	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63734396	CAAACGATTTCAGAC[A/C]AAGTTCTCAGCATGG	8925
rs576625234	snp	G/T	0.00398564	0.0444627	intron-variant	HERC1	GRCh38.p7	15:63748358	AGAATTTGCCATCTT[G/T]AAGAAGAAAACATAC	8925
rs576635381	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63755938	GTCTCTATTAAGATG[C/T]CACCTCTCCTAAGAG	8925
rs576650438	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63612119	CTTGAAGCTAGGAAG[C/T]GGAGGTTGCAGTAAG	8925
rs576654992	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63698528	GTTCTGAGAGATGAC[A/G]ATTTTAAAATGCACT	8925
rs576675769	snp	C/T	0.000202943	0.0100713	intron-variant	HERC1	GRCh38.p7	15:63747716	TACAAAACATACATA[C/T]AACATACCTTGATGA	8925
rs576686795	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63757080	CTTCCTATAAATTCC[C/T]TAGGGTACATTATGG	8925
rs576688650	snp	G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63792609	TAATGTAAAATAATA[G/T]TTAGTATTACCTTCT	8925
rs576714768	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63673003	TTGGTTGTAAGATCT[C/G]ATAAGAGGTTCTCTA	8925
rs576719557	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63805617	TAAAATGGTGAATTT[A/G]TGGTATGTTAATTAT	8925
rs576725429	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63793286	AAAGACCACGCTGAT[A/G]AAACTGGTTGCAGTA	8925
rs576751708	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63656878	TCCAAATCTTGTAGC[A/G]TTGAGCAGTTCGTTT	8925
rs576763433	snp	G/T	0.0349115	0.127424	intron-variant	HERC1	GRCh38.p7	15:63618183	GAATTCATTTTTGTA[G/T]AAGGTGTAAGGAAGG	8925
rs576775380	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63631841	CCACGGCGCCCGGCC[C/T]TCCCAAGTCTTATTC	8925
rs576782909	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63624457	GTCCCAGCACTTTGG[A/G]AGGCTGTGGTGGGCG	8925
rs576788395	snp	A/G	0.000179504	0.00947206	intron-variant	HERC1	GRCh38.p7	15:63656408	GAAAATGGATTTCTT[A/G]AGGGACCATTTGCAG	8925
rs576816798	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63641677	TGCCACATAATAAAT[C/T]TGTTTAAATAAAAAA	8925
rs576824511	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63662887	ATAAAAGACTTTTTA[A/G]AGTGTTTCAACTCTA	8925
rs576829471	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63645312	TACCAAGTTTCACAC[C/T]GGACAACTACTACTC	8925
rs576849149	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63799076	ACATTTAATTTTCAG[A/G]CAAGTTAACTTCAAA	8925
rs576849421	snp	A/G	1.65756e-05	0.00287881	synonymous-codon	HERC1	GRCh38.p7	15:63775159	CATTTCTATAAGTGC[A/G]TCAGTGCTTGACCGG	8925
rs576855064	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63681099	CTTTAATTCTTTACA[C/T]ATAGATTTTAACTAC	8925
rs576858787	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63665345	GAGACCGTCCTGGCC[A/C]ACATGGTGAAACCCT	8925
rs576874325	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63677137	GAAACTTTTTGAGCA[A/C]CAACATGATGCTCAA	8925
rs576876334	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63730228	GGGAGGCCGAGGTGG[A/G]AAGACTGCCTGAGGT	8925
rs576897828	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63813928	GCAGGGCATGGTGGC[A/G]GGTGCCAGTAATCCC	8925
rs576907047	snp	A/T	0.488786	0.0740357	intron-variant	HERC1	GRCh38.p7	15:63739194	AACAACCACTAATAT[A/T]CTTTTTTTTTTTTTT	8925
rs576950212	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63702860	CCTGTAATCCCAGTA[C/T]TTTGGGAGACCAAGG	8925
rs576950454	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63766875	AGAGAAGAGGTTTCT[C/G]CATGTTGGTTCAGGC	8925
rs576959426	snp	C/T			upstream-variant-2KB	HERC1	GRCh38.p7	15:63835801	TGGCCTCCCAAAGTG[C/T]TGGGATTACAGGGGT	8925
rs576974459	snp	A/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63773545	TTTGTATTTTATTTT[A/T]TTTTATTTTATTTTA	8925
rs576987797	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63709523	AAGTACAACAGGCAT[C/T]ATTCTCCACTTCAAA	8925
rs577001058	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63672436	TATTCATATGAGGAC[A/G]ACTGTGCCTTCAGAA	8925
rs577010031	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63752484	TATGAGCCTTTATAA[A/G]GGCTCATAAAATTCT	8925
rs577010345	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63652668	CCATTCCTTTCTTTT[C/G]TTGAGATGAAGTCTT	8925
rs577020468	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63709050	GCTGGAGTGCAGTGG[C/T]GCCATCTCGGCTCAC	8925
rs577020955	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63768154	ATCTCTGATTCTATT[C/T]GACTGTTTCTCTTAT	8925
rs577076084	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63751736	TATTTTTTTCACGCA[C/T]ATATATTTGATTTCA	8925
rs577083012	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63775858	GCCTGGCCAACATTA[A/T]GAAACCCCATCTCTA	8925
rs577087531	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63695239	ACAGGGTTTCGCCAT[A/G]TTGTCCAGGCGGGTT	8925
rs577094832	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63633765	AAGTACTAAAGGTAA[A/G]TTATTTCCAACTAAT	8925
rs577119991	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63828701	AACTATAATGTTTCA[C/T]ATGCCAAAAAATAAT	8925
rs577147384	snp	A/T	6.6486e-05	0.00576529	synonymous-codon	HERC1	GRCh38.p7	15:63659833	CTGAACTGGTTCTGG[A/T]ACAATGCGCCGGTCA	8925
rs577152161	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63790115	GGATAATAAAAGAAC[C/T]TCTATCATTGCCATG	8925
rs577177896	in-del	-/GA	0.0693013	0.172766	intron-variant	HERC1	GRCh38.p7	15:63619048	TTGAATAGGAGTGGT[-/GA]GAGAGGGCATCCCTC	8925
rs577191280	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63659185	AACACCAAGTTTTTT[C/T]TTAAATAACAAGTTC	8925
rs577198236	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63657325	GGTCTCAAACTCCTG[C/G]CTCAAGGGTTCTTCC	8925
rs577209938	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63609842	ATCCATTCAACTGAC[A/G]GTGATGCATCATTTA	8925
rs577232203	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63647232	GCACTCCAGCCTGGG[C/T]GAAAAAGCTAGACTC	8925
rs577237085	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63832292	GTGTGTGTGTGTCTC[C/T]ATACATATATACGTA	8925
rs577237887	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63778430	GTTTAAGACAGCAGG[C/T]GCAATTTAAAAAGAC	8925
rs577243919	snp	C/T	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63643845	AGAGACAGGAAAATA[C/T]TGACTACTTTTTAAC	8925
rs577254813	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	HERC1	GRCh38.p7	15:63834918	AAGTTTGCAATCCAA[C/T]TGGAGGCGTAGGAGA	8925
rs577262518	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63742223	TTAAATGTATTCCTA[A/C]GTATCCTATTCTTTT	8925
rs577267456	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63822153	CCCTGGGAGTCTGCC[C/T]GGCCCGGTCAGGGAA	8925
rs577268000	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63653189	CTCACACCTGTAATC[C/T]CAGCACTGTGGGAGG	8925
rs577286970	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63828322	CAAGGAGAGAGTGAC[A/G]CTTTTCAGTACAACT	8925
rs577310363	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63688226	GTCACATTTTAAAGA[C/T]GAGCCAACAGAATCT	8925
rs577313384	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63789262	CGCCCGGCTAATTTT[C/T]TGTATTTTTAGTAGA	8925
rs577325368	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63778952	AAAGAAAAAGAAGAA[A/G]AGGAAAGGAAGAAAG	8925
rs577338186	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63809549	AATGAAGAGAAAGAA[G/T]GGCCAGGACACAACA	8925
rs577373273	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63810031	ATAAATTATACACAT[A/T]TACTAGAATTCAAGG	8925
rs577375343	in-del	-/TATAGGTAATCACC	0.00199481	0.0315187	intron-variant	HERC1	GRCh38.p7	15:63777790	ATGAATTCTAGATTA[-/TATAGGTAATCACC]TATACAAAACCACCT	8925
rs577375482	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63627121	CTGAAATTGTCAGTG[C/T]GTAGGCAGCTCTGCT	8925
rs577404045	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63762368	TGGTCTTATTGCTCA[C/G]GCTGGAGCACAGTGG	8925
rs577409173	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63771696	CCTCGGCCTCCCAAA[A/G]TGCTGGGATTACAGG	8925
rs577439579	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63626503	ATATTTAATAATTGT[C/T]ATCTTCATAATACCA	8925
rs577448223	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63829309	ACATCTGTAGTCCCA[A/G]CTACTTGGGAGGCTG	8925
rs577450072	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63752274	ACCACTGCCTGACAC[A/G]AGGTGGCCTCCTATA	8925
rs577472318	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63724496	AAAGTATAATCTTTC[C/T]CATTTTGTTTTGTTT	8925
rs577477971	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63779185	AAATACAAAACAAAC[A/G]AAAACAGAGCTGGTT	8925
rs577501988	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63710462	GTTATTTATAAATTT[A/G]AAAATAATTTCCTGA	8925
rs577528157	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63644528	TTTTTGCTTTTTACC[C/T]TCTCCAAACCTTCTA	8925
rs577529453	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63649061	TCATTTTTTAAAAGA[C/T]AATTTCATCTCGGCC	8925
rs577529826	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63684911	CTAATTGGGAGGCTG[A/G]GGCAGGAGAATCGCT	8925
rs577540639	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63717688	CCAGCCTGGTCAACA[C/T]GGTGAAACCCCATGT	8925
rs577548195	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63785675	TCAGCAGGATGAGGT[G/T]GGATGATCCCTTGCG	8925
rs577590495	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63786397	CAACAATTCGACTCC[C/T]AGATCTATACCCAAG	8925
rs577606942	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63831649	ACCCAGCCCCCTTTT[C/T]TTTCTATTTCAAATA	8925
rs577607071	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63822535	AGGTTGCAGTGAGCC[A/G]AGATCATGCCACTGC	8925
rs577622339	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63800840	TGAGGTGACTCTTAG[C/T]GGGCCCTTAGATAGC	8925
rs577626568	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63786311	AAGAAGAAGAAGAAT[C/T]GAAAGACAGCTGTGA	8925
rs577646045	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63815991	GCATGAGGGTAACCA[C/T]CCCCACGATTCATTT	8925
rs577660595	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63779963	AGGTTGCAGTGAGCC[A/G]AGATCACAAGACTGC	8925
rs577670808	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63824743	TGTGATACAAACACA[C/T]TCTGGAATAGTATTC	8925
rs577676098	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63616761	AACAACAGCTATAGC[A/G]TTAGTCTATACCTGT	8925
rs577678585	snp	A/G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63692122	CTGTGCTAAAATATC[A/G/T]TATTAAACAGGATGT	8925
rs577692043	snp	A/G	0.0023933	0.0345097	intron-variant	HERC1	GRCh38.p7	15:63664321	TAAAATTATGTAAAT[A/G]CATAGAAAATGATAT	8925
rs577693705	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63818089	TCCTATATAATAATT[-/A]ACTCTTATTTGCAAG	8925
rs577715433	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63691444	GCACTCCAGCCTGGG[C/T]GACACAGAGAGCCTC	8925
rs577729171	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63663721	TGCCTCCACCTCCCA[A/G]AGTGCTGGGATTATA	8925
rs577733322	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63671577	GTGTACGCTGAAGCC[A/C]CTGTATCAGAATCAC	8925
rs577758759	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63713255	TTCATGTCTATGTTA[A/C]CATCAGAACACTGTA	8925
rs577774751	in-del	-/A	0.00358779	0.0422022	intron-variant	HERC1	GRCh38.p7	15:63799344	GTCTCTCCAAAAATT[-/A]AAAAAATTAGCCAGG	8925
rs577777717	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63791946	TGATTTAATCAACTG[C/T]TTTCCAGTGTAATTC	8925
rs577780450	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63686656	ACTATGAATCAGTTA[C/T]TGTGCAGGGCAACAG	8925
rs577806090	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63621625	CCCACTTTCAGGTAC[A/G]CCAATCAGATGTAGA	8925
rs577806284	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63630090	CCCATATCAACTGAT[A/G]TTCCCAGGACCTAAT	8925
rs577818401	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63637990	GGACTAGCTGAGGTA[A/G]AGAAGAGCAAAAGAG	8925
rs577826205	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63693779	TAACAGACTCTAAGC[A/G]GAGATGTTTGGTCAG	8925
rs577835853	snp	A/T	0.0138799	0.0821421	intron-variant	HERC1	GRCh38.p7	15:63738599	AGGGTCAAAGGAAAA[A/T]GGTGGGAAAGCATAC	8925
rs577877371	snp	A/T	0.0154538	0.0865337	intron-variant	HERC1	GRCh38.p7	15:63735542	TAAAATTTAAAGTAT[A/T]AAAAAAAAAAAAAGA	8925
rs577886603	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63677274	CTGAATTCAAACACA[C/T]CTAAATGCTTTTAAA	8925
rs577888430	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63622681	ATATTTACTCCTTAG[A/G]GTTACAATGAGGACT	8925
rs577897572	snp	G/T	0.00279162	0.0372561	intron-variant	HERC1	GRCh38.p7	15:63685361	CTGTGCTGCCTATTA[G/T]ATGTTCTGATTACAG	8925
rs577908615	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63721775	GTGATTCTGAACAAT[C/T]CCGATCATCGTTAAA	8925
rs577910955	snp	A/T	0.00874735	0.0655527	intron-variant	HERC1	GRCh38.p7	15:63789927	TAAATACTAGAAAGA[A/T]GATGAAGATCACACA	8925
rs577912362	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63833191	AGACTAAACAATGCG[C/T]CCCGCCTCGCCTCCC	8925
rs577962340	snp	A/G	0.00159617	0.0282053	intron-variant	HERC1	GRCh38.p7	15:63609769	GCCTCCTTTGCAGGC[A/G]CCATGGCTGCCTCGC	8925
rs577963263	snp	A/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63610258	TGGCCCAGCAGCCCA[A/T]ATGCACCAGAGCCAG	8925
rs577964108	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63794179	CATAAAAATGAGCAA[C/T]CAGCAGCCCTTGGGG	8925
rs577987893	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63707473	ACCTGTGTATCTGGT[C/G]GGGGGATGTAGACAA	8925
rs578001384	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63727555	TTGATAGCCTTAGGA[C/T]AGATAGACTCCAATG	8925
rs578016168	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63657011	GATTGGTCTTTAGGG[A/G]GCACATATTTAAGTA	8925
rs578023092	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63765333	AAAGGCACAGATCTG[C/T]GTAAACCAAAAATAA	8925
rs578028291	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63767955	TTTCTCCAAGATCTT[C/T]ATAAATTTACTATGT	8925
rs578071057	snp	C/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63616859	CTTCGGCTTCCCTAA[C/T]CACACGTTGAGTTCT	8925
rs578085583	snp	A/G	0.00716266	0.059414	intron-variant	HERC1	GRCh38.p7	15:63759341	AATCATGGCTTATTT[A/G]CCATTTCTGTAGAAT	8925
rs578104616	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63749960	GCGATTTATCATGCT[C/G]CCTTTAGGCATTCAC	8925
rs578111292	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63686070	TTTGCTTCATTTTCA[C/T]TGCTAGAAGAAAATG	8925
rs578115514	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63714378	ATATATGGGGCAAGA[C/T]TGCCTCCAGAGTGAG	8925
rs578117210	snp	C/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63773790	CTCAAGTGATCCACC[C/T]TCCTGAGCTTCCCAA	8925
rs578118532	snp	C/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63616262	CTGCTCTATTAGAAG[C/G]TGTTTAAACTGCTGC	8925
rs578139405	snp	C/G	0.0111196	0.0737302	intron-variant	HERC1	GRCh38.p7	15:63780636	CTGAGGCAGGAGAAT[C/G]GTGTGAACCCGGGAG	8925
rs578162104	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63651796	GTAATCCCAGCATTT[G/T]GGAGGCTGGGGCAGG	8925
rs578171316	snp	G/T	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63736754	TGGGATTACAGGCAT[G/T]CGCCACCATGCCCAG	8925
rs578177431	snp	A/G	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63832596	TTGTAAAAATATAAT[A/G]TATACATAGGTACTA	8925
rs578181059	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63702635	AACATATTTTTACAG[A/G]TTTTGTCAAGAATTT	8925
rs578213666	snp	A/G	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63833496	GACCACAGCGGGGCC[A/G]GGGCACAGACGTTGT	8925
rs578231264	snp	C/T	0.00119737	0.0244387	intron-variant	HERC1	GRCh38.p7	15:63645856	TCCCAATCACTAGAC[C/T]AACTTACCCTTTAAT	8925
rs578241103	snp	A/C	0.000399281	0.0141238	intron-variant	HERC1	GRCh38.p7	15:63645383	AAGAATAGCAACTGG[A/C]AATAAACTCTTTAAG	8925
rs578245636	snp	A/G	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63750748	ACCAGCCTGGACAAT[A/G]TGGCAAGACCCGATC	8925
rs578247028	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63673783	AGGCTTGAGTGCAGT[C/G]GCACAATCTCGGCTC	8925
rs578247429	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63705815	TGGGAGGACTGCTTG[A/C]GCCCAGGAGTTCAAG	8925
rs578254276	snp	C/G	0.0138799	0.0821421	intron-variant	HERC1	GRCh38.p7	15:63742952	GTTTTTCTTTTCTTG[C/G]AATGTTTTGGTCCAC	8925
rs745308769	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63805492	GGAACAGGTGGAGAA[G/T]ATTACAGCCAAGACA	8925
rs745309053	snp	A/G	1.7683e-05	0.00297341	synonymous-codon	HERC1	GRCh38.p7	15:63674565	GTCTGAGTTGTGGCC[A/G]TTTTCAGCCAGAACT	8925
rs745349196	snp	G/T	2.06469e-05	0.00321294	missense	HERC1	GRCh38.p7	15:63649877	CCCTCTTCTGGCCAA[G/T]CCAGGGCAGATACCC	8925
rs745362235	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63654601	CTCACGCCTGTAATC[C/T]CAGTGCTTTGGGAGG	8925
rs745362237	snp	A/G	1.74127e-05	0.0029506	missense	HERC1	GRCh38.p7	15:63656224	CGTGATCGTTCTGAG[A/G]TGCTAGCCATGGCAG	8925
rs745367562	snp	C/T	2.23307e-05	0.00334138	intron-variant	HERC1	GRCh38.p7	15:63633814	TGAAAACTATTTATG[C/T]TGTCTGAAAACCTAG	8925
rs745368170	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63710245	AGTAGGAAAGTAGCA[C/T]AATCAGCAGGTAGGT	8925
rs745376507	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63777542	GAACATCTTATGTTT[C/G]TTGGTCATCTGGATA	8925
rs745392226	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63731714	ACGTAGACCAGACCC[C/T]GAAGAGCCACAGGAA	8925
rs745408860	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63746263	TATTAAATTTATCTT[A/G]TAATTTCTTTCTTTG	8925
rs745415237	snp	C/T	1.68142e-05	0.00289945	intron-variant	HERC1	GRCh38.p7	15:63651239	CAGTTTACTAGTGTT[C/T]ACATGACTCTTACCA	8925
rs745433412	snp	A/G	6.70612e-05	0.00579017	intron-variant	HERC1	GRCh38.p7	15:63634001	CATTCCGTAAGGCAA[A/G]TCACAAGACCTAAAA	8925
rs745439466	snp	A/T	3.48991e-05	0.00417712	intron-variant	HERC1	GRCh38.p7	15:63749325	TTTTTATTGGTGTTT[A/T]TGTTAAAACACACAA	8925
rs745439886	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63830449	AACAAAAACTGAGGA[A/C]CTGTCAGAGATTGGA	8925
rs745441416	snp	A/G	0.000414034	0.0143821	synonymous-codon	HERC1	GRCh38.p7	15:63674922	ATCCCCTTTCTCCTC[A/G]GATTCATGTCGGTGT	8925
rs745447209	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63745044	CATGTCTAGAAATGT[C/T]ATCTGAGAGCTGGCA	8925
rs745454337	snp	A/T	1.65828e-05	0.00287943	missense	HERC1	GRCh38.p7	15:63640171	AGAAATACAAGTTCA[A/T]CCTCTGGAACAGGTT	8925
rs745455881	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63622468	CTCCCAAGTAGCTGG[A/G]ATTACAGGCATGTGC	8925
rs745460108	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63732501	TGAATTTAAGAAACA[C/T]TAGAGATTTAGAATT	8925
rs745476424	snp	A/G	2.63362e-05	0.00362869	missense	HERC1	GRCh38.p7	15:63694078	GTACACCAGTTTGGG[A/G]CAATAAATTCTTCAA	8925
rs745477964	snp	C/T	1.65666e-05	0.00287802	synonymous-codon	HERC1	GRCh38.p7	15:63775489	CAAAGGTACTACTTC[C/T]TTATTGCTAACCAGT	8925
rs745511362	in-del	-/CGCGCGCG			intron-variant	HERC1	GRCh38.p7	15:63833744	CCGGCAAAGCACACA[-/CGCGCGCG]CGCACACACACACAC	8925
rs745514157	snp	A/G	3.35357e-05	0.00409472	missense	HERC1	GRCh38.p7	15:63713359	CAGTCCCACCTGGTC[A/G]TAAGTCCACCCCCTT	8925
rs745528402	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63636501	GTCATGAACTCCTGA[A/C]CTCAAGTGATCCGCC	8925
rs745534559	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63800911	ATAAAAGTGTTGGAA[C/T]TTTCAGTTCCACCAC	8925
rs745561829	snp	A/G	1.84582e-05	0.00303789	intron-variant	HERC1	GRCh38.p7	15:63725280	TTTAAATGCTGCAGA[A/G]AAGCACATTACCCAA	8925
rs745566692	in-del	-/TT			intron-variant	HERC1	GRCh38.p7	15:63695385	GAGTCTGTATAATCT[-/TT]TTTTTTTTTTTTTTT	8925
rs745573803	snp	C/G	1.80889e-05	0.00300735	synonymous-codon	HERC1	GRCh38.p7	15:63656109	ACACAACTGTACAAG[C/G]AGTTTGGCAGCACTA	8925
rs745583638	snp	C/T	0.000134077	0.00818662	synonymous-codon	HERC1	GRCh38.p7	15:63677859	CCTGATAGTAATTTC[C/T]GCTTCATCCCATTGG	8925
rs745584112	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63710492	ACTACCTACCACGTG[C/T]TATTATAGGTGCTTG	8925
rs745591417	snp	C/T	1.66699e-05	0.00288698	missense	HERC1	GRCh38.p7	15:63662020	TCAGACTCACAAACA[C/T]GCTGCACAAAAGGAT	8925
rs745602043	snp	C/T	1.74105e-05	0.00295042	missense	HERC1	GRCh38.p7	15:63659895	ATTCTTCTTCACCAG[C/T]TAGCTTTTCATCTTC	8925
rs745622357	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63678805	TACACACTGCAAATA[A/C]GACACAGAAGTAAAA	8925
rs745625935	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63770173	CCCCACAACTCAATC[A/G]CTTTGTGAGCCTCTC	8925
rs745631654	in-del	-/A	3.60289e-05	0.00424419	intron-variant	HERC1	GRCh38.p7	15:63658765	AGGTAAGAAAAAAAT[-/A]ACATCTGAACTACTA	8925
rs745636917	snp	A/C	1.83947e-05	0.00303266	missense	HERC1	GRCh38.p7	15:63643454	CACCAGACACCAGGG[A/C]CAACCCATCAGAACT	8925
rs745642287	snp	A/G	7.50497e-05	0.00612529	synonymous-codon	HERC1	GRCh38.p7	15:63637569	TTGTCCTAATCTGCC[A/G]TAACTTCCTTCCCCA	8925
rs745642918	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63811637	ACATGGTGAAACCCC[A/G]TCTCTCCTAAAATTA	8925
rs745673428	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63721093	GTGGTATAGAAAACC[C/T]AACTGCACATCCCAA	8925
rs745676697	in-del	-/ATTT			intron-variant	HERC1	GRCh38.p7	15:63657751	CAATAAACTTTATTG[-/ATTT]ATTTTTCTTTTATAT	8925
rs745684469	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63660938	AGGATATATAAAAAA[A/C]CATGTAAAATAAAGA	8925
rs745684574	snp	A/G	1.65652e-05	0.0028779	missense	HERC1	GRCh38.p7	15:63775034	GAGCTCACAACTTCA[A/G]TTGCAGTATGAATGA	8925
rs745687811	snp	A/G	3.34236e-05	0.00408787	synonymous-codon	HERC1	GRCh38.p7	15:63628813	GGTATGGCCTAAGCC[A/G]AGCTGGGAATAAATC	8925
rs745695425	snp	C/T	3.46554e-05	0.00416251	missense	HERC1	GRCh38.p7	15:63718659	ACTTTGTATACACAA[C/T]GGTACACTTCTGATA	8925
rs745703716	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63833572	CGGCTTCTACGCTGC[G/T]CCGAGGCGCCCGGGC	8925
rs745713858	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63676914	CAATTATGTAGAGTC[A/G]TTAGACAAATGAGTC	8925
rs745715534	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63648257	TGTCATTGTCTGACT[C/T]AAAAGACAGAGACTT	8925
rs745720924	snp	C/T	1.65908e-05	0.00288012	synonymous-codon	HERC1	GRCh38.p7	15:63749414	ATGTGATGTTCCAGC[C/T]GAAATCTGCTGAATA	8925
rs745721037	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63810616	TTTCTTAACATTTGC[A/G]TATATTGCTTCTTTT	8925
rs745727166	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63689715	CTGTTTTATTGAAGA[A/C]AAAAGGATAAAATTT	8925
rs745732176	snp	C/G	2.05198e-05	0.00320304	missense	HERC1	GRCh38.p7	15:63643049	CAACAGTTTGCAAGA[C/G]AGAGCCATCCTAAAA	8925
rs745747487	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63716156	TGTAGGAGCCCCTGT[C/G]AGCTAATACAAATTG	8925
rs745748562	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63769233	AACCAGCCTGGCCAA[A/C]ATGGCAAAACCCCGT	8925
rs745750454	snp	G/T			missense	HERC1	GRCh38.p7	15:63623841	CTGAAGCATTCAGCT[G/T]AACTACTTGTCTCGC	8925
rs745761009	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63809862	TCTGCTTTTTTAAAA[C/T]AGAGATAAGGTCTCA	8925
rs745761319	snp	A/T	1.66801e-05	0.00288787	missense	HERC1	GRCh38.p7	15:63612535	GAACAATCCAGGACA[A/T]CCCTTCTCGGACTGC	8925
rs745766115	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63782720	ATCTGGGTAAAGTCA[A/G]TAGAAAATGTTCTGG	8925
rs745775662	snp	G/T	2.10175e-05	0.00324165	intron-variant	HERC1	GRCh38.p7	15:63694911	TGAATTACACATAAA[G/T]AATTACTTTTTCTAT	8925
rs745785326	snp	A/G	8.33021e-05	0.00645322	synonymous-codon	HERC1	GRCh38.p7	15:63674721	TTTGGACATGTGTTC[A/G]TGATTTTTTCTTTTC	8925
rs745794496	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63781455	TGTTATGGTAACCTG[C/T]AATCAGCAAGCTTTG	8925
rs745803563	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63647299	AAAAAACACAATGAG[A/G]TATCATCTCACCCCA	8925
rs745805531	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63658949	TATTTACCATAGGAG[G/T]ATTTATACTTAATTT	8925
rs745820904	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63809545	AGATAATGAAGAGAA[A/G]GAATGGCCAGGACAC	8925
rs745822250	snp	C/T	5.43454e-05	0.00521246	intron-variant	HERC1	GRCh38.p7	15:63612599	ATGAGTGTGCGTGAA[C/T]CTGGCACCCACCAAG	8925
rs745828701	snp	A/G	1.76846e-05	0.00297354	intron-variant	HERC1	GRCh38.p7	15:63689722	ATTGAAGAAAAAAGG[A/G]TAAAATTTGTAAAAA	8925
rs745835061	snp	A/G	3.31384e-05	0.00407039	synonymous-codon	HERC1	GRCh38.p7	15:63666023	GCCACTGCCTAGAAC[A/G]GCTGCTCCAGGCCTA	8925
rs745860024	snp	C/G	1.6684e-05	0.00288821	intron-variant	HERC1	GRCh38.p7	15:63659723	ATCAATGCAAATCAG[C/G]ATTTCAGTTTACCTA	8925
rs745873921	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63821934	GGTAGGCAAGTAATT[C/G]TATTTCAGGAAGCAT	8925
rs745875724	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63735872	AGGACAAATCTTTAA[C/T]GACTTTCTCAGAGTA	8925
rs745883306	snp	A/G			upstream-variant-2KB	HERC1	GRCh38.p7	15:63834905	CTCTGCGTTCCAGAA[A/G]TTTGCAATCCAATTG	8925
rs745888118	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63671703	CCAGGTGGCCTTGGG[A/C]ACACCAAAAATTGAG	8925
rs745889008	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63629635	GGAAACTCCCAAAGG[C/T]GCCTTCAACATTAAC	8925
rs745896684	snp	A/G	1.94941e-05	0.00312197	synonymous-codon	HERC1	GRCh38.p7	15:63672660	TGTCTGTGCCTGCTG[A/G]GCAGGGTCACTTTCT	8925
rs745903917	snp	C/T	4.96824e-05	0.00498385	missense	HERC1	GRCh38.p7	15:63663136	ACAACGCCCCTGGGT[C/T]TTGCTGCAAAGATAT	8925
rs745905579	in-del	-/TATAAC			intron-variant	HERC1	GRCh38.p7	15:63665802	ATGCCCATCTTTTCA[-/TATAAC]TATATTTATCAACTT	8925
rs745910923	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63763350	TGGAAGAATACATGT[A/T]TACAGACATAACACC	8925
rs745918660	in-del	-/CCTA	1.65957e-05	0.00288055	intron-variant	HERC1	GRCh38.p7	15:63725513	ATTAGTTCTGGCCCT[-/CCTA]AAGACAAAATCATTA	8925
rs745920362	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63627752	CAACATTAAGGTAAC[A/G]GCTACATCTGGAAGG	8925
rs745928647	snp	A/G	0.000192024	0.00979669	intron-variant	HERC1	GRCh38.p7	15:63749319	TTCTACTTTTTATTG[A/G]TGTTTATGTTAAAAC	8925
rs745935739	snp	A/G	1.65619e-05	0.00287762	missense	HERC1	GRCh38.p7	15:63640316	ATGCAGGGTCAGGGA[A/G]ACAGTTCTGGTGGTG	8925
rs745946355	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63716097	CCAGAGCTTCTCAGC[C/G]CTGAATATGTAACCC	8925
rs745951885	snp	A/G			intron-variant, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609334	GGAGTGGGGCTGCCC[A/G]TGACCTCTCCCTGCC	8925
rs745961379	snp	A/G	1.76101e-05	0.00296728	intron-variant	HERC1	GRCh38.p7	15:63656396	CAGATGGATAAAGAA[A/G]ATGGATTTCTTAAGG	8925
rs745963113	snp	C/T	6.66478e-05	0.0057723	missense	HERC1	GRCh38.p7	15:63640418	TATAGGGGCTATGAA[C/T]AAGTTGGTCACCACA	8925
rs745970588	in-del	-/AAT			intron-variant	HERC1	GRCh38.p7	15:63694934	TTTTCTATTAGCAAC[-/AAT]AATACCTGCTTGCAA	8925
rs745982745	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63650630	GTTATAGAAGAGAGT[A/G]TAAAGAAAAACACTG	8925
rs745996075	snp	C/T	1.66513e-05	0.00288537	intron-variant	HERC1	GRCh38.p7	15:63623690	TGGCCACTAGCAGAC[C/T]AGATAACTCAGCAGG	8925
rs746000498	snp	A/C	1.65622e-05	0.00287764	missense	HERC1	GRCh38.p7	15:63725424	GCCCAATAAGGAGAG[A/C]AATTGTTCTTTCTAG	8925
rs746000806	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63670717	CTGATCTTGTGTGGA[C/T]GCCTTGAATTCTGTA	8925
rs746001055	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63804150	AAAATGATTCACAGA[C/T]CGAAACGTAAGAGCT	8925
rs746019323	snp	A/G	8.3212e-05	0.00644973	missense	HERC1	GRCh38.p7	15:63640415	GCATATAGGGGCTAT[A/G]AACAAGTTGGTCACC	8925
rs746029933	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63626380	AAAATAAAATGTCTT[C/T]ATTATTATGGAAATG	8925
rs746056097	snp	A/G	1.7238e-05	0.00293576	intron-variant	HERC1	GRCh38.p7	15:63630432	TGTGAGATTTCTAGA[A/G]TATGAGAAAGCAGCA	8925
rs746059923	snp	A/G	1.66751e-05	0.00288744	synonymous-codon	HERC1	GRCh38.p7	15:63755260	TCCTTCACCCCATGT[A/G]TATAATTCCCCATCC	8925
rs746067253	snp	A/T	1.7557e-05	0.0029628	intron-variant	HERC1	GRCh38.p7	15:63699031	ACATATATCAATGGC[A/T]ATCAAGTAGAGCATA	8925
rs746071314	snp	A/G	1.67789e-05	0.00289641	intron-variant	HERC1	GRCh38.p7	15:63718760	AGCAAATATTTGTCT[A/G]AGGATAGTTTTAAGT	8925
rs746090803	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63824577	CCACCATATGATCCA[A/G]CAATCTCTCTTCTCG	8925
rs746098639	snp	A/G	1.65658e-05	0.00287795	missense	HERC1	GRCh38.p7	15:63677966	GACCTCCAACTCTAA[A/G]ACCAGCATCAACTCC	8925
rs746118384	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63639272	TTAAGATTATAAAAC[C/T]TTATTTTTATTATAT	8925
rs746126844	snp	A/T	1.72302e-05	0.0029351	intron-variant	HERC1	GRCh38.p7	15:63712735	ATATCATATACCTTG[A/T]AAACAAAAATCTTTC	8925
rs746133935	snp	C/T	5.476e-05	0.0052323	synonymous-codon	HERC1	GRCh38.p7	15:63694338	GGCTAGAATCTGGAG[C/T]AACCTTGTACTGGCC	8925
rs746135091	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63727983	CTGGTAGCTGATGTA[A/G]TATCAGTGTTTATTC	8925
rs746165548	snp	A/G	0.000209853	0.0102412	intron-variant	HERC1	GRCh38.p7	15:63694304	ACAAAGACATCTACC[A/G]TACTTACCCAGTAGT	8925
rs746196321	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63651465	AAAATAAGGGTTTCA[C/T]ATAGACTAGAGTGTA	8925
rs746201983	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63759826	AGAGGATAGGGTCAT[A/C]TTGGTCAGATACTTT	8925
rs746209028	snp	A/T	2.75486e-05	0.00371127	intron-variant	HERC1	GRCh38.p7	15:63764207	CTATAATTAAAACAT[A/T]GCGGGACACAGCGTA	8925
rs746209914	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63730004	GCACTCCAGCCTGGG[A/C]GACAAGAGTGAAACT	8925
rs746216094	snp	A/G	5.98964e-05	0.00547217	synonymous-codon	HERC1	GRCh38.p7	15:63749786	TCCACAGCCCCAAGC[A/G]TAGACCTGAAAAAAA	8925
rs746218739	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63615053	GGGAAAGGGAAATCC[A/G]TGTGAGGTCATAAGA	8925
rs746224148	snp	A/T	1.88763e-05	0.0030721	synonymous-codon	HERC1	GRCh38.p7	15:63652443	ACAGGTCTGTTGCAG[A/T]GAATATTGCTTCTTG	8925
rs746226509	in-del	-/ACAC			intron-variant	HERC1	GRCh38.p7	15:63718084	GGCAGCTATTATGTG[-/ACAC]ACACACACACACACA	8925
rs746235549	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63829173	CATGGAATCCCAACA[C/G]TCTGAGAGGCCAAGG	8925
rs746238188	snp	C/T	0.000150604	0.00867636	intron-variant	HERC1	GRCh38.p7	15:63635924	AACAACTAGTATATT[C/T]ACAATGAAAGGCAAA	8925
rs746243190	snp	C/T	1.65693e-05	0.00287826	synonymous-codon	HERC1	GRCh38.p7	15:63666408	GAACCCCATTTCCAG[C/T]AAGGGAACTGCAATT	8925
rs746255337	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63692740	AGGTCAGAAAACAAA[C/G]CCTAAACTTGAAACG	8925
rs746263072	snp	A/C	1.6571e-05	0.0028784	intron-variant	HERC1	GRCh38.p7	15:63644981	AGTCTTCAAAAACAC[A/C]AGAATGTTACCTGGC	8925
rs746265796	snp	C/T	1.65633e-05	0.00287774	missense	HERC1	GRCh38.p7	15:63716370	GGATGCCCCTCTTCC[C/T]GGTCTCTCTCAGCCT	8925
rs746280065	snp	C/T	1.70504e-05	0.00291975	intron-variant	HERC1	GRCh38.p7	15:63752909	TACTTTTTAGTCACC[C/T]AATCCTCTGAAATAC	8925
rs746280736	snp	G/T	3.44881e-05	0.00415245	missense	HERC1	GRCh38.p7	15:63626107	TCAGCGCCCCATACT[G/T]GGGGGGCACTGTGTC	8925
rs746290424	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63755390	TAGTCCGTATTTGAT[A/C]CTATACACAGAGACT	8925
rs746301906	snp	A/G	2.03647e-05	0.00319092	missense	HERC1	GRCh38.p7	15:63696314	GACAATAGAACGAGG[A/G]TCTGATGAAGTGCCT	8925
rs746303058	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63663465	ATAATGTTTTTGTTG[A/C]TGTTTTTAGAGACAG	8925
rs746309766	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63650321	GGAGGCTGCAGTGAG[A/C]CGAGATCACGCCACT	8925
rs746316499	snp	A/G	1.65679e-05	0.00287814	missense	HERC1	GRCh38.p7	15:63725489	GGTAATGGCAGACCA[A/G]CAGGATCAATTAGTT	8925
rs746328257	snp	C/T	1.75533e-05	0.00296249	intron-variant	HERC1	GRCh38.p7	15:63641453	GTGTATCTCTAGGAG[C/T]GAGTGTAATGAGTTA	8925
rs746342911	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63825955	TTTAGTAGAGACGGG[A/G]TTTCACCATGTTGGC	8925
rs746357766	snp	C/T	1.71143e-05	0.00292521	intron-variant	HERC1	GRCh38.p7	15:63686347	CTAAAAACTATTAGA[C/T]TTTCTACGTACCTTC	8925
rs746416325	snp	G/T	1.68275e-05	0.0029006	intron-variant	HERC1	GRCh38.p7	15:63716279	CACAGTTTGTATCTA[G/T]AAAGTAAGAAGGGTA	8925
rs746418432	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63631698	GGCGCCTGCCACCAC[A/G]CTCGGCTAATTTTTG	8925
rs746436413	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63720693	AGAATGACAATCCTC[A/T]TCAGGCTCTTAGGAA	8925
rs746436807	snp	C/T	1.65649e-05	0.00287788	synonymous-codon	HERC1	GRCh38.p7	15:63686473	ACACTGAGCTTTCTC[C/T]GGGTCAAAGGATACT	8925
rs746448212	snp	A/G	1.67694e-05	0.00289558	missense	HERC1	GRCh38.p7	15:63658551	ACACTTACCTGACTG[A/G]GAGAAGAGACAGCGC	8925
rs746448719	snp	C/T			missense	HERC1	GRCh38.p7	15:63754601	CTCCTACATTGCTGA[C/T]GTCTTTTACTAATGT	8925
rs746458171	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63796674	GGATATCAATCAATA[C/T]TTGTAAAATGTCCAT	8925
rs746463334	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63807759	CTACCAATTCCTACA[A/T]CACTCAGTTGAGATA	8925
rs746480651	snp	C/T	5.21635e-05	0.00510676	intron-variant	HERC1	GRCh38.p7	15:63630661	CAAAACAAAAACATG[C/T]GGAAATGTTATGCAC	8925
rs746490074	snp	C/T	3.33918e-05	0.00408592	missense	HERC1	GRCh38.p7	15:63651376	TTTCCTCAGCATCCC[C/T]TTCCCTAGAATATAA	8925
rs746498512	snp	C/G	1.65759e-05	0.00287883	missense	HERC1	GRCh38.p7	15:63749452	CATCTAAGCCACTCA[C/G]TTTCTTTGGTTTAGT	8925
rs746500375	snp	C/T	5.15983e-05	0.00507902	intron-variant	HERC1	GRCh38.p7	15:63764049	AAATACATGCCATAG[C/T]ATTTTAACACAAAGT	8925
rs746531551	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63719434	GACATCAGAGAGCTG[A/G]CTGGGGACCAGATCC	8925
rs746534316	snp	A/G	1.94407e-05	0.00311769	synonymous-codon	HERC1	GRCh38.p7	15:63659926	ATCAACATCCAACAT[A/G]TCCCAGTCTTCTGGA	8925
rs746534401	in-del	-/TTT			intron-variant	HERC1	GRCh38.p7	15:63697451	TGATGTTAATCTTGA[-/TTT]TTTTTTTTTTTTTTT	8925
rs746534415	snp	A/G	1.70936e-05	0.00292344	synonymous-codon	HERC1	GRCh38.p7	15:63666119	CATGGCAAGGACAGT[A/G]ATATTCTGGGCATCA	8925
rs746571019	snp	C/T	0.000165618	0.00909843	missense	HERC1	GRCh38.p7	15:63686451	TCTGTCCATTCTCCA[C/T]TAGGCAACACTGAGC	8925
rs746577352	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63776032	GACAAAGCGAGACTC[C/T]GTCTCAAAAAAAAAA	8925
rs746580382	snp	C/T	1.87366e-05	0.00306071	intron-variant	HERC1	GRCh38.p7	15:63615727	TCATTTGGAGAGAAA[C/T]CCAAGCATTCATGTG	8925
rs746583824	snp	C/T	8.50203e-05	0.00651943	missense	HERC1	GRCh38.p7	15:63696159	CACTCTCTCCCTTGC[C/T]TCCTGTGTGTCCAAC	8925
rs746586572	snp	A/G	3.53851e-05	0.0042061	synonymous-codon	HERC1	GRCh38.p7	15:63749672	AGCCAAACAATGACT[A/G]TCTCCAATAGAAACA	8925
rs746588160	snp	A/G	0.000167968	0.00916275	intron-variant	HERC1	GRCh38.p7	15:63625945	GGCACTGCTTACCAA[A/G]CCAGTCTGTGCCTGG	8925
rs746589153	snp	C/T	4.97047e-05	0.00498496	synonymous-codon	HERC1	GRCh38.p7	15:63713517	GTACACATCCTGACC[C/T]TCAGGAAGGTCTGTG	8925
rs746590070	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63819934	AAGGTTTTACCCCAT[A/G]AGTTTAAACGTGCGT	8925
rs746590315	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63644094	TAGTACTCCCACCTC[C/T]ACTGCTGTGATATTC	8925
rs746594036	snp	C/G	1.87023e-05	0.0030579	missense	HERC1	GRCh38.p7	15:63729296	GCAAATTTGCAGAAC[C/G]TGAATAAATATCTGT	8925
rs746597087	snp	C/G	2.53952e-05	0.00356328	intron-variant	HERC1	GRCh38.p7	15:63634683	TAAGCGAACACAGAA[C/G]AAATGAGAAACAATG	8925
rs746605595	snp	C/G	1.65666e-05	0.00287802	synonymous-codon	HERC1	GRCh38.p7	15:63725380	CTCTGGAGACACAGG[C/G]GAGCCCTGAAGCATG	8925
rs746611134	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63778726	CGATACCACAAAAAC[A/G]AACATGAGAAAACTC	8925
rs746611339	in-del	-/GAC			intron-variant	HERC1	GRCh38.p7	15:63625191	TAGTCCATAAAGATA[-/GAC]AAATCAGCAAAATTT	8925
rs746643927	snp	A/C	1.66007e-05	0.00288098	intron-variant	HERC1	GRCh38.p7	15:63694941	TTAGCAACAATAATA[A/C]CTGCTTGCAAAAAGA	8925
rs746645994	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63791215	TTAATAACTTCTCAT[C/T]GTGTGTATGTACAGA	8925
rs746656688	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63685495	CTGGCCAGAGTTGTC[C/T]AGTGCTAAATTGATG	8925
rs746658762	in-del	-/CC			intron-variant	HERC1	GRCh38.p7	15:63754940	GACTTGTTTTCATTA[-/CC]CACTAGATTATAAAC	8925
rs746668389	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63777885	AATTAAAATAAATTC[C/T]ACATTCATCTGGAAG	8925
rs746681629	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63623953	CCCCAAAATCACATG[A/G]TATCTTCCCATCAGT	8925
rs746721227	snp	A/C	1.72633e-05	0.00293791	intron-variant	HERC1	GRCh38.p7	15:63656372	CACTGCCAGTAAAGA[A/C]AAACATCTCAGATGG	8925
rs746721473	snp	C/G	1.67699e-05	0.00289563	missense	HERC1	GRCh38.p7	15:63651262	TCTTACCATTAACTT[C/G]CCAGATATTCACCAT	8925
rs746737458	snp	C/T	1.65883e-05	0.00287991	missense	HERC1	GRCh38.p7	15:63678124	ATTTCATTTTCCTCT[C/T]GGCTCTGAACCGAGC	8925
rs746746372	snp	A/C	5.03495e-05	0.00501719	missense	HERC1	GRCh38.p7	15:63755316	ATCCAGCTGACACAC[A/C]AACAACTACCTGCAT	8925
rs746756647	snp	A/G	6.99864e-05	0.00591509	missense	HERC1	GRCh38.p7	15:63655780	TCATAGTTAGGTCTT[A/G]GTTTGGCCCCTTTGT	8925
rs746758180	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63653984	AACATCTTTGTAATT[A/G]TGTGCATGTGTATGT	8925
rs746773544	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63622612	TGCTGGAATTACAGG[C/T]GTAAGCCACCATGCC	8925
rs746775221	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63759532	AAAAGGAAGATGCCC[C/T]TATCTTAACTTCACA	8925
rs746777908	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63667193	AGATGCACAAAACAA[C/G]ATTATACAGCATACT	8925
rs746800086	snp	A/T	1.70351e-05	0.00291843	intron-variant	HERC1	GRCh38.p7	15:63630451	GAGAAAGCAGCAAGC[A/T]ATATAAATATTTACC	8925
rs746802569	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63789916	AAGAATCCAGCTAAA[A/T]ACTAGAAAGAAGATG	8925
rs746811533	snp	C/G	3.54931e-05	0.00421251	missense	HERC1	GRCh38.p7	15:63648163	CCCACTGCAAATGGT[C/G]TGTCTTCACTGAACC	8925
rs746821952	snp	C/G			missense	HERC1	GRCh38.p7	15:63666416	TTTCCAGCAAGGGAA[C/G]TGCAATTGCTGGAGG	8925
rs746822894	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63700195	TCATTTTATATCACC[-/T]TTTTGGACACACTCT	8925
rs746823738	in-del	-/AC			intron-variant	HERC1	GRCh38.p7	15:63763412	CAATTTATAGGAAAT[-/AC]AGAGGATAAAGAAAC	8925
rs746849559	in-del	-/AAA	0.000335089	0.0129396	intron-variant	HERC1	GRCh38.p7	15:63674315	CAACAGCACAAAAGC[-/AAA]AAAAAAAAAAATCAG	8925
rs746849763	snp	A/G	5.91081e-05	0.00543604	missense	HERC1	GRCh38.p7	15:63655921	GAGTCATCAACTGTG[A/G]TTAGATTTACACCTG	8925
rs746850847	snp	C/T	8.28123e-05	0.00643423	missense	HERC1	GRCh38.p7	15:63630543	GTTCAGCTCCAACTG[C/T]CACATCTTCTATGAT	8925
rs746859330	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63636561	CAGGCATGAGCCACA[G/T]TAACCGGCCTAATTT	8925
rs746860839	snp	A/G	1.66012e-05	0.00288103	intron-variant	HERC1	GRCh38.p7	15:63729477	TGATAGATCACCATA[A/G]AAGACAAATAATCGC	8925
rs746863410	snp	G/T	6.76556e-05	0.00581577	intron-variant	HERC1	GRCh38.p7	15:63712765	CTTTACTGAATCTGG[G/T]TATACCTACCAGTGC	8925
rs746863800	snp	C/G			missense	HERC1	GRCh38.p7	15:63680160	AAGCTAATTTGGGTT[C/G]CTACAGTGTGGCAGC	8925
rs746878096	snp	C/T	3.51853e-05	0.00419421	intron-variant	HERC1	GRCh38.p7	15:63756415	ATCTAATTATTTTTA[C/T]AACCAAAAAGAATGC	8925
rs746888105	in-del	-/CAAAA	0.000232169	0.0107717	intron-variant	HERC1	GRCh38.p7	15:63660960	AAATAAAGAAGCTCT[-/CAAAA]CAAACTACCTTCATA	8925
rs746891901	snp	C/T	1.65655e-05	0.00287793	missense	HERC1	GRCh38.p7	15:63775041	CAACTTCAATTGCAG[C/T]ATGAATGACATCGTT	8925
rs746914974	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63723713	ACAAAAAACCAACGC[A/G]TTCAAAATGGAATGA	8925
rs746917734	snp	C/T	3.83899e-05	0.00438104	missense	HERC1	GRCh38.p7	15:63615820	CTCTCCACATATTCC[C/T]TCCTGTTGGAAAATG	8925
rs746926196	snp	A/C/G			intron-variant	HERC1	GRCh38.p7	15:63649093	GGCACGGTGGCTCAC[A/C/G]CCTGTAATCCCAGGA	8925
rs746932986	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63690843	CATGCTTATGCCTCA[A/G]TTTTTATGTATACAT	8925
rs746933443	snp	C/T	1.66643e-05	0.0028865	missense	HERC1	GRCh38.p7	15:63690588	CACAAGCTGGCAGCA[C/T]AGCTTCAAGGACATG	8925
rs746938438	snp	A/G	1.77307e-05	0.00297742	intron-variant	HERC1	GRCh38.p7	15:63692367	CTTAATAAAATGCAA[A/G]TAATATCTATAAATA	8925
rs746946569	snp	C/T	1.65842e-05	0.00287955	missense	HERC1	GRCh38.p7	15:63718799	GGCTTTCTCCACATG[C/T]TTGACTAAGTAAATT	8925
rs746949194	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63635206	GCATGTGCTACCACA[C/T]CTGGCTATTTATTTC	8925
rs746977703	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63811665	TTATACAAAATTAGC[C/T]GGGTGTGGTGGCAGG	8925
rs746982333	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63833799	CACACACAGGACCAG[A/G]AGGACGGTAGATGAT	8925
rs746986701	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63723648	TCTGGCGTTTTGGCA[A/G]GCAGAGGCCAGAGAA	8925
rs747012563	snp	G/T	1.68122e-05	0.00289928	intron-variant	HERC1	GRCh38.p7	15:63660943	ATATAAAAAAACATG[G/T]AAAATAAAGAAGCTC	8925
rs747014138	snp	C/T	5.09593e-05	0.00504748	missense	HERC1	GRCh38.p7	15:63664569	TTCCAGAAGCTGCAT[C/T]CTCTGTATGATCCAA	8925
rs747031186	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63811174	ATTTAAACACAAATG[C/T]TGCATATTAGGTGAC	8925
rs747054714	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63782854	CCTACGGATGACTTT[C/G]AGAGGTTCAAGACTT	8925
rs747062736	snp	C/G	1.67038e-05	0.00288992	missense	HERC1	GRCh38.p7	15:63658559	CTGACTGAGAGAAGA[C/G]ACAGCGCTCTCATGA	8925
rs747062790	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63648390	TACTTTTTAAAAGTG[C/T]CGCTTATCTGTGACA	8925
rs747079292	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63752428	GAGTGAAAATACGCA[A/T]GTAAAAGTTCGAAGC	8925
rs747088936	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63611101	GGAAAGGGGTGTGAA[A/G]AAGGACTTACTAAAG	8925
rs747092293	snp	A/G	2.0448e-05	0.00319743	synonymous-codon	HERC1	GRCh38.p7	15:63652461	ATATTGCTTCTTGGT[A/G]ACATTCCATACGCGG	8925
rs747093785	in-del	-/G	2.03901e-05	0.0031929	intron-variant	HERC1	GRCh38.p7	15:63753108	ACAAACACATTAAAC[-/G]AATTTACTTGTTTTA	8925
rs747096247	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63705310	AGGTGCATGCATCCA[C/T]GCCTAGCTTTTTTTT	8925
rs747121389	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63631925	TCTCATTCTATACTC[A/T]CTCTCTCTGGGTTTT	8925
rs747124430	snp	A/G/T	0.000115946	0.00761319	missense, synonymous-codon	HERC1	GRCh38.p7	15:63612374	GAACTCTTCCAGCGT[A/G/T]TGCCAGAACCACTGC	8925
rs747129477	snp	C/G	4.37742e-05	0.00467816	missense	HERC1	GRCh38.p7	15:63727671	GCCACTGTAACTCCT[C/G]GTCTTCTAAAAGATC	8925
rs747131856	snp	A/C	3.32823e-05	0.00407922	intron-variant	HERC1	GRCh38.p7	15:63635946	AAAGGCAAACTTATC[A/C]ATTTCCTGCCTGACC	8925
rs747138132	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63688910	GGTTTGAGGGGGAGA[C/T]ACCCAGGCTAGCATT	8925
rs747139588	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63794990	AGAATTGTTTGAACC[C/T]GGGAGGCGGGGGTTG	8925
rs747152695	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63659064	GAATTACCAATACTG[A/C]CCAATTCTTTATTTT	8925
rs747155630	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63823095	GTACAGATTATTTCA[C/T]CACCCAGGTATTAAG	8925
rs747168477	snp	G/T	1.71634e-05	0.0029294	missense	HERC1	GRCh38.p7	15:63640441	TCACCACAAACCACA[G/T]GAGGCTAAAACAAAA	8925
rs747174189	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63803729	TTAAATGATCTCAAT[G/T]GGGTAACAAAAGAAG	8925
rs747178456	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63610280	CAGAGCCAGTGATGA[C/T]ACAGCTCAACGCAGA	8925
rs747185404	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63750808	CATTGTGGCACAGGC[A/C]TGTGGTCCCAGCTAC	8925
rs747187464	in-del	-/AACA			intron-variant	HERC1	GRCh38.p7	15:63736107	TTGGAAACAGAAAGG[-/AACA]GACAAAGGGTAACTG	8925
rs747188181	snp	C/T	5.63063e-05	0.00530566	intron-variant	HERC1	GRCh38.p7	15:63746896	GGTTTGAGATACAGA[C/T]TCACAAGTCCTATTC	8925
rs747189212	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63803839	AGAGAAAACATTAAA[A/G]ATGTACATTATCTGA	8925
rs747195510	snp	A/C/G	0.000126831	0.00796257	intron-variant	HERC1	GRCh38.p7	15:63649707	CTCCGTCAGCTAGAC[A/C/G]TAAGTGCAGTCATTT	8925
rs747196454	snp	A/G	1.66186e-05	0.00288254	intron-variant	HERC1	GRCh38.p7	15:63623707	GATAACTCAGCAGGG[A/G]ACACTGCAGGAATAT	8925
rs747199351	in-del	-/A	5.4371e-05	0.00521369	intron-variant	HERC1	GRCh38.p7	15:63729377	TTGAGTTCTAAGAAG[-/A]AAAAAAGTTCCTAAA	8925
rs747199659	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63629066	AGCAATTTTCTGCCT[C/T]AGCCTCCCAAGTGGC	8925
rs747217311	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63672024	GGCTAAAGAAGCATC[A/G]TAAGACATGCCCTTT	8925
rs747221185	in-del	-/AGTT			intron-variant	HERC1	GRCh38.p7	15:63668113	ATTTAATTCAAAGAA[-/AGTT]AATTAATTCAAAAGA	8925
rs747221621	snp	G/T	1.99051e-05	0.0031547	missense	HERC1	GRCh38.p7	15:63672666	TGCCTGCTGGGCAGG[G/T]TCACTTTCTTCAGCT	8925
rs747226698	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63627832	CACAAGTATGTATTA[C/T]GGTTTTCTTTAAATC	8925
rs747227268	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63702991	TGCCTATAATCCCAG[A/C]TACTCAGGAGGCTGA	8925
rs747234336	snp	C/T			upstream-variant-2KB	HERC1	GRCh38.p7	15:63834959	CATACAAGCCATGAA[C/T]GTGTCACTAATGTAA	8925
rs747250206	snp	A/G	1.6612e-05	0.00288196	intron-variant	HERC1	GRCh38.p7	15:63725518	TTCTGGCCCTCCTAA[A/G]GACAAAATCATTAGT	8925
rs747261958	snp	C/T	3.42413e-05	0.00413757	intron-variant	HERC1	GRCh38.p7	15:63694578	AGACAGTTAAGAATC[C/T]TCCTTTCAGTAAACA	8925
rs747262286	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63794236	TTTCATTCCTTTACT[G/T]TCTTAATAAACTTGC	8925
rs747272870	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63653237	CCTGAGGTCAGGAGT[C/T]TGAGACCAGCCTGGC	8925
rs747289459	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63642159	ATCAGCACATCGGCT[C/T]TAATCTTTAAGGGTA	8925
rs747299831	snp	C/G	5.04868e-05	0.00502403	intron-variant	HERC1	GRCh38.p7	15:63664438	CAAAATAAGATCTTT[C/G]ACAAAGAAAAGGATA	8925
rs747302087	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63762469	GCTGGGATTACAGAC[A/G]TCTGCCGCCCCACCC	8925
rs747303511	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63683839	TTTAACTGCTGCCCC[A/G]AAAAGCTGCTGGCTT	8925
rs747335874	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63670766	AACCATATTAGAATG[G/T]CGTATCAGGCAAGCA	8925
rs747336247	snp	A/G	1.66963e-05	0.00288927	intron-variant	HERC1	GRCh38.p7	15:63669497	TCCCACACATCTGGA[A/G]TGCCAACTTTGGATA	8925
rs747342773	snp	C/T	3.4712e-05	0.00416591	missense	HERC1	GRCh38.p7	15:63693994	TCTCAGTTTCTCCAC[C/T]GGAGTCAACTTTTTT	8925
rs747351566	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63696388	CTTAACTCAGACATG[A/G]TGAAACTCTGTATGC	8925
rs747355718	snp	A/G	1.72794e-05	0.00293928	synonymous-codon	HERC1	GRCh38.p7	15:63753072	TCTGTTGGTATCACC[A/G]TGACCAAGTTTACCT	8925
rs747355848	snp	C/T	1.65638e-05	0.00287778	missense	HERC1	GRCh38.p7	15:63645095	AAGCCACTCTGACAG[C/T]CACTTAAAAAAATTG	8925
rs747374730	snp	A/G	3.33372e-05	0.00408258	synonymous-codon	HERC1	GRCh38.p7	15:63775359	ATACCATCTTTGCCA[A/G]TGCTAGCTGGCTGCT	8925
rs747391229	snp	A/G	6.62317e-05	0.00575426	missense	HERC1	GRCh38.p7	15:63661913	GGCGGTTTGCACTGC[A/G]CCCACAGCCTGGATG	8925
rs747394270	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63815649	ATCAAAAGTTTCTCC[A/G]TATCACTGTAGTGAA	8925
rs747409272	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63670590	AGACAGAAGAAATGA[C/G]GAGTCATAAGTCCTG	8925
rs747429095	snp	C/T	1.70069e-05	0.00291602	synonymous-codon	HERC1	GRCh38.p7	15:63626114	CCCATACTGGGGGGG[C/T]ACTGTGTCAGGCAGG	8925
rs747430535	snp	A/G	3.31647e-05	0.00407201	intron-variant	HERC1	GRCh38.p7	15:63638779	ATTTACTGTTATCCT[A/G]AAAAACAGGGGGTAC	8925
rs747443236	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63828311	GATAGTAAAAACAAG[A/G]AGAGAGTGACACTTT	8925
rs747444687	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63820099	TCATGTAGCACACAA[A/G]AAATACATACAATTT	8925
rs747464639	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63762489	CCGCCCCACCCAGCT[A/G]ATTTTTTGTATTTTT	8925
rs747465543	snp	C/T	4.96907e-05	0.00498426	missense	HERC1	GRCh38.p7	15:63636092	TTTCAGTTAGGGCCA[C/T]AGAGTGCCCATCAGA	8925
rs747465689	snp	C/T	3.31235e-05	0.00406948	missense	HERC1	GRCh38.p7	15:63674970	GGTGCTCTGTTTGCC[C/T]ATGTCTTCATGAACG	8925
rs747466701	snp	A/C/G	8.29145e-05	0.00643826	missense	HERC1	GRCh38.p7	15:63616474	TGTCTTCAATGTGAA[A/C/G]AATGCTGTTGAGAGT	8925
rs747468169	snp	A/G	3.31312e-05	0.00406995	synonymous-codon	HERC1	GRCh38.p7	15:63775021	TAATGGTGGCAAAGA[A/G]CTCACAACTTCAATT	8925
rs747474503	snp	C/G	8.37507e-05	0.00647057	intron-variant	HERC1	GRCh38.p7	15:63752926	ATCCTCTGAAATACT[C/G]TAAGTCTTTTATACT	8925
rs747474808	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63639596	AATGTTTATCCAAAT[A/G]TTTGTATACATAAAT	8925
rs747481210	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63785551	AGGTGGGCGGATCAC[C/T]TGAGCTCAGGAGTTC	8925
rs747507542	in-del	-/TACTTCTATTTGTTTTTTCCATT			intron-variant	HERC1	GRCh38.p7	15:63730136	TAAAATTCATCAAGC[-/TACTTCTATTTGTTTTTTCCATT]AAAAAAAAAAAAGCA	8925
rs747520714	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63706030	CAAGACCCTGTCTCC[-/A]AAAAAAAAAAAAAAA	8925
rs747524091	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63814661	TTTAGTAGAGACAGG[A/G]TTTTGCCATGTTGGC	8925
rs747525071	in-del	-/CCCCATT	1.67075e-05	0.00289023	frameshift-variant	HERC1	GRCh38.p7	15:63616610	TGTGCGAATGGCAAC[-/CCCCATT]AAAATTCCTAAAAAC	8925
rs747546478	snp	C/T	1.72293e-05	0.00293503	intron-variant	HERC1	GRCh38.p7	15:63686580	TGGAATAATCCATGT[C/T]TCAGATAAGATATAT	8925
rs747559050	snp	C/T	1.88856e-05	0.00307285	intron-variant	HERC1	GRCh38.p7	15:63626200	GGAAACAGCATTGCT[C/T]TCACTTTTCACATTT	8925
rs747565573	snp	A/G	1.65767e-05	0.00287891	synonymous-codon	HERC1	GRCh38.p7	15:63666438	TGCTGGAGGAGGAGG[A/G]GAAGTTGAAAGTCTA	8925
rs747583985	snp	C/T			synonymous-codon	HERC1	GRCh38.p7	15:63756734	GACAAAAGTGCAGTA[C/T]TGTCCAGCTTCAATC	8925
rs747591711	in-del	-/CA			intron-variant	HERC1	GRCh38.p7	15:63690918	CTATGCTACACATTT[-/CA]CACACATACATTCTA	8925
rs747599524	snp	C/T	1.66776e-05	0.00288765	synonymous-codon	HERC1	GRCh38.p7	15:63675060	ATCAAACGGCAATGG[C/T]TCACAGGGTTCCAGA	8925
rs747609203	snp	C/T	1.65877e-05	0.00287986	intron-variant	HERC1	GRCh38.p7	15:63660958	TAAAATAAAGAAGCT[C/T]TCAAAACAAACTACC	8925
rs747616073	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63742180	TAATGTTTTGTTCCT[C/T]CAGTGTACAAGTCTT	8925
rs747619561	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63663547	TGTAACCCTGAACCC[C/T]TGGGCTCAAGACATC	8925
rs747621504	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63617815	ATGTCTTCTTTTGAG[-/A]AGTGTCTGTTCATAT	8925
rs747628969	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63633151	ACATTTTAGCTTTTA[C/T]GGGCGACAATAACTG	8925
rs747631903	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63726735	AGATAGTTTCACAGA[C/T]AAATTCTTCTAAAAC	8925
rs747634748	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63638786	GTTATCCTGAAAAAC[-/A]GGGGGTACATAATGA	8925
rs747642423	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63709439	CCATTGATCTGTTGT[C/T]CCCATTTATAATTTT	8925
rs747644472	snp	C/G	0.00011597	0.0076139	missense	HERC1	GRCh38.p7	15:63666389	TGGCAATCTGCCGAA[C/G]AGAGAACCCCATTTC	8925
rs747646678	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63827288	TTAGCCAGGTATAGC[A/G]GTGCACACTTGTAGT	8925
rs747647452	snp	G/T	1.65902e-05	0.00288008	intron-variant	HERC1	GRCh38.p7	15:63644949	TCTGATGTCATATAC[G/T]TTCCATAGTTTCAGA	8925
rs747649992	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63797749	CTGCGCAGCAGGCAG[A/G]GAAAACCTGTCAGGA	8925
rs747654019	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63811927	CCATGTTCTTCCTGA[G/T]GGAGCATATGTAATA	8925
rs747659863	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63675848	CTATTTTCCTCTAGG[C/T]TCATTTTTCTTGTTT	8925
rs747664709	snp	A/C	0.000104756	0.0072365	missense	HERC1	GRCh38.p7	15:63655808	TGTCTGCTAGCAATG[A/C]CACAAGGGCCTGTGT	8925
rs747666464	snp	C/T	5.04367e-05	0.00502153	intron-variant	HERC1	GRCh38.p7	15:63661735	GGAGGTCTGGATATC[C/T]ACACAATTTCAAGGT	8925
rs747672627	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63719960	TGGTATTTGATGCCA[-/T]TAAAAGTATATACTG	8925
rs747675431	snp	C/T	1.73525e-05	0.0029455	intron-variant	HERC1	GRCh38.p7	15:63752901	ACAAGTATTACTTTT[C/T]AGTCACCTAATCCTC	8925
rs747679586	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63798706	TGAGGAATGGATTCC[A/C]CCTTATTTTAATTCT	8925
rs747685285	in-del	-/A	5.24939e-05	0.00512291	intron-variant	HERC1	GRCh38.p7	15:63624113	AATAACATCCATCTG[-/A]AAAAAATCACAGCTC	8925
rs747714857	snp	A/G	4.83173e-05	0.00491491	missense	HERC1	GRCh38.p7	15:63749728	CTTCAATAAGCTTGG[A/G]TCTCAAAGCAGTAGC	8925
rs747718219	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63631790	AGGTGATCCACCCGC[C/T]TCGGCCTCCCAAAAT	8925
rs747726303	snp	C/G	1.6577e-05	0.00287893	missense	HERC1	GRCh38.p7	15:63718853	GAACAAATCTAGACA[C/G]AGTGTCCAAGAGTGA	8925
rs747736470	snp	A/G	2.16997e-05	0.00329384	synonymous-codon	HERC1	GRCh38.p7	15:63643497	CCGAACAGGAGTGAT[A/G]TGTCCCCGCAGCTGA	8925
rs747742466	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63808797	AGTATACTTTCTAGA[A/G]GAATGAAGATCCTGA	8925
rs747748584	snp	C/T	4.4963e-05	0.00474125	intron-variant	HERC1	GRCh38.p7	15:63615952	ACAGAATTTTTATTA[C/T]ATGGTAGAAATGACA	8925
rs747749384	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63687630	GCCAGGTATCCTATC[A/G]GGTCCTCCATATTTA	8925
rs747759485	snp	A/T	2.13472e-05	0.00326698	missense	HERC1	GRCh38.p7	15:63615851	TGAGTGGGATACTAT[A/T]TCCACCAGGGATTAT	8925
rs747778484	snp	A/G	5.11697e-05	0.00505789	missense	HERC1	GRCh38.p7	15:63696173	CCTCCTGTGTGTCCA[A/G]CAGTGCCTAAACCAA	8925
rs747784750	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63720980	GTCTATGCTTACAGT[A/G]TATAAGCAATACAAC	8925
rs747790124	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63807938	CCCTCAATTATCTTT[C/T]TTATCTTGGAATTTC	8925
rs747794166	snp	A/C	1.88525e-05	0.00307016	missense	HERC1	GRCh38.p7	15:63666141	TGGGCATCAGCCTCT[A/C]CCCTAGCACCTATAC	8925
rs747830803	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63821181	AATCCCAGCACTTTG[C/G]GAGGCTGGGGTGAGA	8925
rs747833491	snp	C/G	1.90456e-05	0.00308585	missense	HERC1	GRCh38.p7	15:63696299	TTTTCTTCCATCCCA[C/G]ACAATAGAACGAGGA	8925
rs747852140	snp	A/C			utr-variant-3-prime	HERC1, FBXL22	GRCh38.p7	15:63608861	TATGGAGGGAAAAAC[A/C]TGACTGAGAGCACTT	8925
rs747856897	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63776551	AAAAATACTTCAATC[-/A]AAATAGTGGTTGCCT	8925
rs747862975	snp	C/T	3.67728e-05	0.00428778	missense	HERC1	GRCh38.p7	15:63649733	CATTTACCATCCTTT[C/T]GATAGCAATGCTCCA	8925
rs747872296	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63741437	TCAAGCAATTCTCCT[A/G]CCTCAGCTGGGATTA	8925
rs747877524	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63701087	TCTAGTTACTAATAC[C/T]TATAAATTACTTTTC	8925
rs747878464	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63628988	TGGAGTCTTGCTCTG[-/T]TGTCCAGGCTGGAGT	8925
rs747879912	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63819984	CGCTAAGAGAGTGGA[G/T]GTTAAGTGTTCTCAC	8925
rs747915995	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63686747	ACAGAAGACAAATAC[A/G]TACTGCTAGTATTAC	8925
rs747921467	snp	A/G	6.84322e-05	0.00584905	synonymous-codon	HERC1	GRCh38.p7	15:63756617	GGATCTGTGAGGCTC[A/G]AATGTTAACTTTTTT	8925
rs747928629	snp	C/T	1.71755e-05	0.00293044	synonymous-codon	HERC1	GRCh38.p7	15:63641509	AAGCATCATGGGGAG[C/T]CGCTCCAAAAATGCT	8925
rs747942097	snp	A/G	1.68303e-05	0.00290084	missense	HERC1	GRCh38.p7	15:63623880	CAAAAATAGGCTTAC[A/G]CTTCCGTCCTCTTTA	8925
rs747945731	snp	C/G	5.86734e-05	0.00541602	intron-variant	HERC1	GRCh38.p7	15:63664615	AGTGCAAGTGAGAAA[C/G]CAACACAAAGTTTTT	8925
rs747950930	snp	A/G	3.31598e-05	0.00407171	missense	HERC1	GRCh38.p7	15:63623744	CACATCTCTGTGATG[A/G]TGTCATCAAACACTC	8925
rs747952028	snp	A/C	1.77735e-05	0.00298101	intron-variant	HERC1	GRCh38.p7	15:63694593	TTCCTTTCAGTAAAC[A/C]AAGCATTTATTAAAA	8925
rs747952769	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63792749	ATCTTGCAGCAGACG[C/T]TAGCTGGGTGTCTTC	8925
rs747973587	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63779159	ATATTATTGGATTAC[A/G]TGAGGAAGAAAAATA	8925
rs747979862	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63662884	GAGATAAAAGACTTT[C/T]TAGAGTGTTTCAACT	8925
rs747985189	snp	C/T	1.6599e-05	0.00288084	missense	HERC1	GRCh38.p7	15:63775307	TGGAGTACAAGCAGT[C/T]GTTTTCTAAGTGCCC	8925
rs747994113	snp	G/T	3.80474e-05	0.00436145	synonymous-codon	HERC1	GRCh38.p7	15:63649849	AGACTCTCCTGACCA[G/T]GCTGTAGCCGGACCC	8925
rs748006919	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63831860	GACGCATTTACATTT[C/G]CTTTCTCTTCCATGC	8925
rs748015990	snp	C/T	9.14746e-05	0.00676232	synonymous-codon	HERC1	GRCh38.p7	15:63747083	AAAACTGTGGTGTTC[C/T]CTGAAACCAAATAAA	8925
rs748019019	snp	G/T	1.65666e-05	0.00287802	missense	HERC1	GRCh38.p7	15:63638742	GCCCAAGACATAATT[G/T]GTTCATCCATGCCGT	8925
rs748021465	snp	A/G	6.91587e-05	0.00588001	intron-variant	HERC1	GRCh38.p7	15:63723175	CCCTTTATCTTCTTT[A/G]TCTTACCTTTACTAA	8925
rs748021736	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63667304	CTAATTCAGTGTTCA[C/T]AATAACCTTTTAGAA	8925
rs748038098	snp	C/T	1.70673e-05	0.00292119	missense	HERC1	GRCh38.p7	15:63712864	TTGGGCTTGTGTGGA[C/T]TAGCCGGCTCTCTGC	8925
rs748042698	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63624380	CTAGGCTTAAAAGAA[A/G]TAACAATTTTCACTT	8925
rs748050941	snp	C/T	1.68391e-05	0.0029016	synonymous-codon	HERC1	GRCh38.p7	15:63756440	GAATGCACATACCTT[C/T]CCTTGTAGAGGTCCC	8925
rs748053443	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63760597	TAAATAAATACAGTA[A/G]ATAATGCCCTAAGAG	8925
rs748059385	snp	C/T	1.65663e-05	0.002878	missense	HERC1	GRCh38.p7	15:63630563	TCTTCTATGATTACT[C/T]CAGCCAGGACAGGGA	8925
rs748070202	snp	A/C/T	0.000117707	0.00767087	missense	HERC1	GRCh38.p7	15:63712780	GTATACCTACCAGTG[A/C/T]GTAACCCTCTTCATC	8925
rs748070722	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63637957	GAAACTCGTACATAA[C/G]AATGAGTCATGCAAT	8925
rs748083821	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63681074	TGTTTAGTCCAGAAA[G/T]TAATGAAAACTTTAA	8925
rs748127748	snp	A/G	3.08371e-05	0.00392652	intron-variant	HERC1	GRCh38.p7	15:63672712	AGAAACCAAAAAAAA[A/G]GTTAAGAAAGTAGTA	8925
rs748128372	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63802002	CTCTCGACGTCTACC[A/T]ACCCATGTCTCCCCC	8925
rs748129391	snp	A/C/T			intron-variant	HERC1	GRCh38.p7	15:63711756	TGACCAAGATCCCAC[A/C/T]GCTCTTTAACAGTAG	8925
rs748142009	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63773298	AAAGTACAAAAATTA[C/G]CCGGGCATGCTAGTG	8925
rs748144670	snp	A/G	5.27023e-05	0.00513307	missense	HERC1	GRCh38.p7	15:63774702	TACGTACCAAAGAAC[A/G]CCTCATCTGCATTAA	8925
rs748150522	snp	A/C	1.73878e-05	0.00294849	intron-variant	HERC1	GRCh38.p7	15:63658749	CTGTTTTGTTCTCAA[A/C]AAGGTAAGAAAAAAA	8925
rs748172224	in-del	-/AA	1.68613e-05	0.00290351	intron-variant	HERC1	GRCh38.p7	15:63694559	GGGCTTCTAAAAGAC[-/AA]AGAGACAGTTAAGAA	8925
rs748179905	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63801253	CAAATTACTCAAAGG[C/T]GAGGGGGTAGTTGTA	8925
rs748199286	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63771946	CTTCATGGAAACCCC[A/G]TCTCTACTAAAAATA	8925
rs748207599	snp	A/G	1.65649e-05	0.00287788	synonymous-codon	HERC1	GRCh38.p7	15:63654179	ATCTCCTCCCATATC[A/G]GCAAGTGTCTGCAGA	8925
rs748225638	snp	A/C	1.65811e-05	0.00287929	missense	HERC1	GRCh38.p7	15:63636126	ACAGGAAGTCACCAG[A/C]TGGGTCACCACAAAG	8925
rs748235245	snp	A/G	3.34364e-05	0.00408865	intron-variant	HERC1	GRCh38.p7	15:63654081	ACTATTTCATCTTAC[A/G]TAACGTGATTAACAC	8925
rs748240143	snp	C/T	1.65685e-05	0.00287819	synonymous-codon	HERC1	GRCh38.p7	15:63774844	AAGAAGATATCGCAA[C/T]GAGCCTCGTTGAGCT	8925
rs748247572	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63671597	ATCAGAATCACTAGA[A/G]AAACTTAATTAAAAT	8925
rs748257516	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63691188	AGTAAGCCAACAGCC[A/G]GGCATGGTGACCCAT	8925
rs748262136	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63737094	GGGAGGCTACTAAAA[A/C]AGGAACACTTCCAGA	8925
rs748276974	snp	A/T	1.9674e-05	0.00313634	intron-variant	HERC1	GRCh38.p7	15:63628644	ACTGCTAAAAAAGAA[A/T]CGCTGCAGGAGCATG	8925
rs748287509	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63673253	ATCCTACAAATAAAC[-/A]ATAACTAAAATATGA	8925
rs748288296	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63725241	ATAGAGAAATCTCCA[A/G]CTGAGGTACAAACAG	8925
rs748300416	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63785733	AAGATCATGCTACTA[C/T]ACTGCAGCCTGGTCA	8925
rs748314484	snp	A/T	9.61123e-05	0.00693159	missense	HERC1	GRCh38.p7	15:63747742	GATGAAGGGAAAGGG[A/T]GTGGGGGAATCTCAC	8925
rs748321703	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63783678	TAAGGCAAAGTACAA[A/C]AGTATATAAACCACC	8925
rs748329455	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63649111	TGTAATCCCAGGACT[C/T]TGGGAGGCCAAGGTG	8925
rs748335433	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63612180	GCCACAGAGTGAGAC[C/T]CTGTCTCAACAAAAA	8925
rs748338705	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63611196	GCAAGCAGCCCATTA[C/T]GACCAGAACATGAGA	8925
rs748339654	snp	A/G	1.71452e-05	0.00292785	missense	HERC1	GRCh38.p7	15:63727713	GGAGTCTATTAAGGC[A/G]ATCAAGAGGTGGCAA	8925
rs748345331	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63690067	TACTTGGAGGCTAAG[A/G]CAGGAGAATCACTTG	8925
rs748345488	snp	C/T	1.65679e-05	0.00287814	synonymous-codon	HERC1	GRCh38.p7	15:63686488	CGGGTCAAAGGATAC[C/T]TCTTGGATAGGAAGA	8925
rs748368342	snp	C/T	3.31472e-05	0.00407093	intron-variant	HERC1	GRCh38.p7	15:63694729	ACCATAACCTCGGGC[C/T]AAAATGTAACCTGCA	8925
rs748371399	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63705560	TTTTTTTTCTATGGA[C/T]GAGAAACCTAACATT	8925
rs748372217	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63824633	AGCACCTCTGAGAGA[C/G]AGCTGCACTCCCATG	8925
rs748377597	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63634252	ATACATGACCCAAAA[A/T]TATTCATTCATATCA	8925
rs748380876	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63660355	TAAATAAATAAATAC[A/C]TACATACATAAAATG	8925
rs748400501	snp	A/G	9.26913e-05	0.00680713	intron-variant	HERC1	GRCh38.p7	15:63689566	ATGCTGTTAAGAAAT[A/G]CCTTTTAGGAAAAAC	8925
rs748431524	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63831029	TCAACATCATGATAA[C/T]CTGCAATACATGCTC	8925
rs748433902	snp	G/T	1.69292e-05	0.00290935	intron-variant	HERC1	GRCh38.p7	15:63665910	AAAGTACAGAAACTG[G/T]AATTTCACCTTTCAC	8925
rs748448990	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63795284	TTATTAAAATATTCT[G/T]CTTGCATTTATCATT	8925
rs748452795	snp	A/G	2.25859e-05	0.00336042	synonymous-codon	HERC1	GRCh38.p7	15:63694314	CTACCATACTTACCC[A/G]GTAGTGATGGCTAGA	8925
rs748455663	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63650173	TTTGGGAGGCCAAGA[C/T]GGGCGGATCACCTGA	8925
rs748455969	snp	C/T			missense	HERC1	GRCh38.p7	15:63718876	AAGAGTGACTCATTA[C/T]TTAAAGTTGCACTGT	8925
rs748465892	in-del	-/TGCTG			intron-variant	HERC1	GRCh38.p7	15:63625208	AAATCAGCAAAATTT[-/TGCTG]ACTTTATTTCCCCGA	8925
rs748468811	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63673494	CAAGGGACTTTGTTT[C/T]GTTAACTGCTGTCTC	8925
rs748477408	snp	A/C	1.77212e-05	0.00297663	missense	HERC1	GRCh38.p7	15:63775621	TGGAATCATAGTTGC[A/C]ATGTTGATTTATCCT	8925
rs748484608	snp	C/T	3.33311e-05	0.00408221	missense	HERC1	GRCh38.p7	15:63680153	TCTTCAAAAGCTAAT[C/T]TGGGTTCCTACAGTG	8925
rs748490261	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63629350	TTCCAAATCTAGCAG[A/G]TGAGTCTTAATGACT	8925
rs748490282	in-del	-/ACA	3.32497e-05	0.00407722	intron-variant	HERC1	GRCh38.p7	15:63754665	TTGGATAAAACACAC[-/ACA]ACAACAAAGAAACAA	8925
rs748493004	snp	G/T	1.70029e-05	0.00291568	intron-variant	HERC1	GRCh38.p7	15:63662054	ATACCAAATGATTAG[G/T]CAATTTAACATAAAA	8925
rs748495924	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63717701	CACGGTGAAACCCCA[C/T]GTCTACTAAAAATAC	8925
rs748500333	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63751207	ACGGAGTTTTGATGC[C/T]AGTATTTTTACTGTA	8925
rs748509887	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63713043	CTCTTGTCTGAGCAC[-/A]AAGACCTTCTCAAAA	8925
rs748510319	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63685077	CACTTTAAATTCAAA[C/T]TGATTGCTGAGCTTC	8925
rs748512517	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63670901	GTCTCTACAAAAAAA[-/T]TTCAAAAAATTAGCG	8925
rs748515826	snp	G/T	5.12256e-05	0.00506065	missense	HERC1	GRCh38.p7	15:63656248	ATGGCAGAAGGGCTG[G/T]TGGAGAGGCCAGCTC	8925
rs748525764	snp	A/G	3.31268e-05	0.00406968	synonymous-codon	HERC1	GRCh38.p7	15:63733124	CTTGCAAACTTGTCA[A/G]GATGATATCCAGTTG	8925
rs748530360	in-del	-/AAA			intron-variant	HERC1	GRCh38.p7	15:63738553	ACAGGTAGTTCAAAT[-/AAA]AAAATTTTTTAAAGA	8925
rs748543860	snp	A/G	1.65666e-05	0.00287802	synonymous-codon	HERC1	GRCh38.p7	15:63775503	CCTTATTGCTAACCA[A/G]TTTAGAATACAGAAC	8925
rs748545462	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63649010	TGTCAGACCAGGAAT[A/T]CCCTGCTTCCCCTTC	8925
rs748562496	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63739076	GTCTATTCAGAGTTG[C/T]GCAACCATCACCACT	8925
rs748563478	snp	C/T	3.31647e-05	0.00407201	missense	HERC1	GRCh38.p7	15:63616479	TCAATGTGAAGAATG[C/T]TGTTGAGAGTCTGCA	8925
rs748578028	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63642423	GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA	8925
rs748590857	snp	C/G	0.000107208	0.00732068	intron-variant	HERC1	GRCh38.p7	15:63633829	TTGTCTGAAAACCTA[C/G]ACTCAAGGCAGTACT	8925
rs748594126	snp	A/C	3.33812e-05	0.00408528	intron-variant	HERC1	GRCh38.p7	15:63669504	CATCTGGAATGCCAA[A/C]TTTGGATATCATAGT	8925
rs748594536	snp	C/T	0.000119433	0.00772671	synonymous-codon	HERC1	GRCh38.p7	15:63725296	AAGCACATTACCCAA[C/T]TGAGGAGTGTCCATT	8925
rs748596648	snp	A/C/G	3.31286e-05	0.00406982	missense, synonymous-codon	HERC1	GRCh38.p7	15:63733022	AAGGTTGATCTGACA[A/C/G]ATTTCCGTAGCCAGT	8925
rs748597837	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63731549	GTTCTTATCCATTTG[C/T]AGCCATTACTCCTTA	8925
rs748603472	snp	C/T	1.72904e-05	0.00294022	missense, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609116	CCTCGGCGTTGTCCA[C/T]GTTTCTCGAGAGCAT	8925
rs748603693	snp	A/G	9.94448e-05	0.00705071	missense	HERC1	GRCh38.p7	15:63628746	CAGCCGAGATCTGCC[A/G]AACATTTTTCCCTTG	8925
rs748605757	snp	A/T			missense	HERC1	GRCh38.p7	15:63775215	CTGCTGAACCAGAAC[A/T]GCTCTCCGGAGAATG	8925
rs748606621	snp	C/T	1.82947e-05	0.00302441	missense	HERC1	GRCh38.p7	15:63645490	CAACATACGTAGCCA[C/T]CAGTAACTGCAACTT	8925
rs748627307	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63764062	AGCATTTTAACACAA[A/T]GTTGTTAATACAAAA	8925
rs748628494	snp	C/T	0.000149114	0.00863335	missense	HERC1	GRCh38.p7	15:63698921	AAGGAATAGGAGGAG[C/T]TGCATAACCAGTCTC	8925
rs748637998	in-del	-/AAAAAAAAAAAACAAAAAAACCAATTT			intron-variant	HERC1	GRCh38.p7	15:63821736	GTCTCAAAAAAAAAA[-/AAAAAAAAAAAACAAAAAAACCAATTT]AAAAAAAAAAAAAAT	8925
rs748647000	snp	A/G	0.000132463	0.00813721	synonymous-codon	HERC1	GRCh38.p7	15:63661941	ATGGTTTCTCTTCAT[A/G]TGCTGATTGAAGCTG	8925
rs748650272	snp	A/C	1.65509e-05	0.00287666	missense	HERC1	GRCh38.p7	15:63754569	AGCAATAGTATGTGA[A/C]CTGCCACAAGAAACC	8925
rs748683575	snp	A/G	1.69499e-05	0.00291112	synonymous-codon	HERC1	GRCh38.p7	15:63698995	TTGACTGTGCATAGG[A/G]CCTATATACAAACAG	8925
rs748689386	in-del	-/TGTT			intron-variant	HERC1	GRCh38.p7	15:63618795	CATGATTTGGCTCTC[-/TGTT]TGTCTGTTATTGGTG	8925
rs748693076	snp	A/G	3.33728e-05	0.00408476	missense	HERC1	GRCh38.p7	15:63616600	GAGGCTTCTTTGTGC[A/G]AATGGCAACCCCCAT	8925
rs748702274	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63652578	GTCTAATAATTTTCT[A/G]TTCAAATGATTTTAT	8925
rs748707344	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63776500	ACCCAACAATTCCTC[C/T]TCTAAAGATTTATCC	8925
rs748722729	snp	C/T	2.32507e-05	0.00340952	intron-variant	HERC1	GRCh38.p7	15:63655992	CAGACTTAATTTTTA[C/T]ATGTAATTTTGGAAC	8925
rs748725799	snp	A/G	3.31252e-05	0.00406958	missense	HERC1	GRCh38.p7	15:63669627	GGAGAGGTTGGTAAC[A/G]AAGATATTGGAGGAG	8925
rs748741688	snp	A/G	1.72166e-05	0.00293394	missense	HERC1	GRCh38.p7	15:63678271	ATGAGCTGAATAGTG[A/G]CCTCAGCCAGCACTG	8925
rs748747697	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63829128	GGTTTTAAATATATA[C/T]AGAATACAGGCAGGG	8925
rs748751770	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63815933	GGGGGAAAGCCCCTT[G/T]TAAAACCATCAGATC	8925
rs748757671	snp	C/T	3.31466e-05	0.0040709	missense	HERC1	GRCh38.p7	15:63775451	GGCAACTGTGGTCCT[C/T]TGAGGCATAAAACTT	8925
rs748777808	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63695038	TCATATATAAAGTAT[A/G]TAATAATTTTTTTTT	8925
rs748781821	snp	A/T	1.65671e-05	0.00287807	missense	HERC1	GRCh38.p7	15:63638752	TAATTTGTTCATCCA[A/T]GCCGTTAATCCATTT	8925
rs748784296	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63791318	GAGCATCTCCTTGGT[A/G]TATTATGCTGGGACT	8925
rs748798519	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63786112	AATAAGAATGGAAAG[A/G]CAAGCTAGATGCACT	8925
rs748799207	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63706092	AAATGCTTAAGAGAG[G/T]TTTTAGTTATCATTG	8925
rs748815197	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63710190	TGTAATTTGGACTTG[A/C]GTGGACTAGCCATCT	8925
rs748818451	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63743648	CATTTATCAGCTCCA[A/G]AATTTCTACTTGATT	8925
rs748824076	snp	G/T	1.66183e-05	0.00288251	synonymous-codon	HERC1	GRCh38.p7	15:63775318	CAGTCGTTTTCTAAG[G/T]GCCCCGGCAAATGGG	8925
rs748825277	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63756938	CTCACAACTTTGTTG[C/T]TGAGTTCAAATTCTT	8925
rs748827138	snp	G/T	1.75946e-05	0.00296598	intron-variant	HERC1	GRCh38.p7	15:63729668	AAATGACACACAAAG[G/T]AAGTTTATATTTGAA	8925
rs748829364	snp	G/T			missense	HERC1	GRCh38.p7	15:63634777	TCACTCTCTCTGGAA[G/T]TTTTTTGTTAGAGGT	8925
rs748836788	snp	A/G	0.000113613	0.00753614	missense	HERC1	GRCh38.p7	15:63723281	CAGCAATTTCAGGCC[A/G]CAATTTATAATCAAA	8925
rs748838373	snp	A/C/T	3.6175e-05	0.00425282	missense	HERC1	GRCh38.p7	15:63656105	GTGTACACAACTGTA[A/C/T]AAGCAGTTTGGCAGC	8925
rs748846665	snp	C/T	6.98544e-05	0.00590951	missense	HERC1	GRCh38.p7	15:63756637	TTAACTTTTTTAAAG[C/T]TGACTGATTATTGGA	8925
rs748862999	in-del	-/T	3.68718e-05	0.00429355	intron-variant	HERC1	GRCh38.p7	15:63656057	CAGAAATAATCAATG[-/T]TAACGGGGAAAAGTA	8925
rs748864010	snp	A/C/T	3.54373e-05	0.00420923	synonymous-codon, missense	HERC1	GRCh38.p7	15:63698746	TGCCCTTAACTGCTG[A/C/T]TGTTCCATTGCAATG	8925
rs748869376	snp	A/G	4.97987e-05	0.00498968	intron-variant	HERC1	GRCh38.p7	15:63638583	TCATCCATTCACTCA[A/G]ACAGCCATGTACTAC	8925
rs748878192	in-del	-/TT			intron-variant	HERC1	GRCh38.p7	15:63621075	CGTTAGTTGATGCAG[-/TT]TCTTCCTAGCCTCGA	8925
rs748880719	snp	G/T	1.66882e-05	0.00288857	missense	HERC1	GRCh38.p7	15:63753042	TAAAGCTTCAATAAC[G/T]TTAGGTTTATACACT	8925
rs748881741	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63615445	AAAACCCCATCTCTA[A/C]CAAAAAATAAAAAGA	8925
rs748905335	snp	A/C	1.71661e-05	0.00292963	intron-variant	HERC1	GRCh38.p7	15:63616385	TTCTAGTCTGTGCAT[A/C]TAGGACGTCAACACC	8925
rs748933292	snp	A/G			synonymous-codon	HERC1	GRCh38.p7	15:63692547	ATGGAGTTCGGCTGC[A/G]TGTTGTTTCCTAAGA	8925
rs748939957	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63723392	CCAATTTTAACATCA[A/T]AAATTTTGGTGCTAC	8925
rs748971673	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63798825	AAATGGTAACTCATA[A/G]GTATATTAAGGTCAG	8925
rs748974934	snp	C/T	5.23013e-05	0.0051135	intron-variant	HERC1	GRCh38.p7	15:63692615	AGAGCCAACAAGAAA[C/T]AGTCTTATATCACAT	8925
rs748977967	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63664970	TGAAAATATTCACTG[A/C]GCTTGTTGGAAAAAG	8925
rs748980137	snp	C/T	8.50449e-05	0.00652037	intron-variant	HERC1	GRCh38.p7	15:63666518	AAATATCACTAGATA[C/T]CGTGAGTAAAAAGTG	8925
rs748980636	snp	A/G	6.0033e-05	0.0054784	missense	HERC1	GRCh38.p7	15:63689629	TCCTTTATCTGAATA[A/G]CATGTTTGGCCTGAG	8925
rs748991260	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63722163	GAGCCACTGTGCCCA[A/G]CCTATAAAATTAATT	8925
rs748991540	snp	A/G	1.65726e-05	0.00287855	missense	HERC1	GRCh38.p7	15:63732989	GGTGGGTATCTGGAT[A/G]GCAGCTCTGAGTGCC	8925
rs749016443	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63688515	GAGTCTGAATAAGGT[G/T]TCTTTGAGAAGAAAT	8925
rs749026672	snp	A/G	1.95204e-05	0.00312407	intron-variant	HERC1	GRCh38.p7	15:63694897	CTCTGATCCCATCCT[A/G]AATTACACATAAAGA	8925
rs749042505	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63676035	TAGCTCCCTGAGTAG[C/T]TGGGATTACAGGCGC	8925
rs749052545	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63637779	AAAGGGAAGAGTTGA[-/T]ATAACTATGCAGTCC	8925
rs749064556	snp	A/G	5.05813e-05	0.00502872	intron-variant	HERC1	GRCh38.p7	15:63651225	AAAACTACTTTCAGC[A/G]GTTTACTAGTGTTTA	8925
rs749064559	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63781410	TTGGTAATTCTTACA[A/G]TATTTCAAACTTTTC	8925
rs749072913	snp	C/G	0.000112076	0.00748502	intron-variant	HERC1	GRCh38.p7	15:63747862	GCAACAACTTGTCTA[C/G]AAGGACACATAAGAA	8925
rs749078682	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63767824	ATCTAACAAGTTCTC[C/T]CTCTGCCTTCAAAAG	8925
rs749091996	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63772982	TGGTTTGAAAATAAA[C/T]TCAACATAATTGGAT	8925
rs749092644	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63609854	GACGGTGATGCATCA[C/T]TTAAAATGATAATTA	8925
rs749099790	snp	C/G	1.65825e-05	0.00287941	missense	HERC1	GRCh38.p7	15:63612520	ACAGCAGCGGCACAG[C/G]AACAATCCAGGACAT	8925
rs749103426	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63687912	GATTACTGTGTTCAA[A/G]AACTACAAGAAGAAG	8925
rs749110220	snp	C/T			utr-variant-3-prime, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63608993	ATGTTCTTATAACAT[C/T]TATGTAGTTACCATA	8925
rs749112100	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63796026	AATTGTGGGAGCTAA[G/T]AACATAAAGTACATT	8925
rs749114422	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63734302	TGTACTATTTTAAGG[C/T]ATATAAGATAAAAAT	8925
rs749123230	snp	C/G	1.94392e-05	0.00311757	missense	HERC1	GRCh38.p7	15:63643039	GAGCCTATCACAACA[C/G]TTTGCAAGACAGAGC	8925
rs749131866	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63735636	GGAGCTGCATTATCT[C/T]AGGCCTCATAACTTC	8925
rs749136297	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63743538	AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCA	8925
rs749143773	in-del	-/GT			intron-variant	HERC1	GRCh38.p7	15:63832272	AGGTGCAGAATACGT[-/GT]GTGTGTGTGTGTGTG	8925
rs749144826	snp	A/G	1.70391e-05	0.00291878	intron-variant	HERC1	GRCh38.p7	15:63758126	ATGCAAATAAGCATG[A/G]ATATACACCAGATTA	8925
rs749164025	snp	C/T	3.32917e-05	0.0040798	intron-variant	HERC1	GRCh38.p7	15:63727863	GCAAGAAATTAAACA[C/T]GGGACAATTGCTTCA	8925
rs749165888	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63657633	GGTTTTCTATTTTAT[C/T]GTATTCCAATTTATC	8925
rs749171208	snp	A/T	2.06307e-05	0.00321168	intron-variant	HERC1	GRCh38.p7	15:63632843	TAAGGCACACAACTT[A/T]AAGAAGAAAAAAAAT	8925
rs749182762	snp	G/T	3.42742e-05	0.00413955	intron-variant	HERC1	GRCh38.p7	15:63624151	AAACACACATACATA[G/T]GCTAACCTGGTTGAT	8925
rs749184119	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63748932	GCAAAAATTAACCTC[C/T]TTGATTTAAAGTATG	8925
rs749192147	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63780355	ATACAAAGACAGAAC[A/G]GGAAATGAATCAAAG	8925
rs749201768	snp	A/T	0.000348815	0.0132017	intron-variant	HERC1	GRCh38.p7	15:63713331	TGAGTAGGTCATGTT[A/T]TCAGTGTCTAGTCAG	8925
rs749216793	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63833632	GGGGATCCGCGGCGC[A/G]CCAGGAGGGCTCCCC	8925
rs749217325	snp	C/T	1.65666e-05	0.00287802	intron-variant	HERC1	GRCh38.p7	15:63694748	ATGTAACCTGCACTG[C/T]ACATTTGCAGGAACC	8925
rs749225480	snp	C/T	6.98287e-05	0.00590843	missense	HERC1	GRCh38.p7	15:63674543	GAACAACTGGAGAAC[C/T]TGCACAGTCTGAGTT	8925
rs749237440	snp	A/G	1.66164e-05	0.00288235	missense	HERC1	GRCh38.p7	15:63674413	TAGATCATGGCTTGC[A/G]CTCGTTCCAGATCAG	8925
rs749245157	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63793029	AAGGCTATTACAAAG[G/T]GTATCAATGAACACC	8925
rs749247127	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63656576	TGGCATATACTTGAA[A/G]TACAATTGAACTGAC	8925
rs749253437	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63670644	GGCATGATTCTACCA[A/C]TGAATCCCATGCCCA	8925
rs749255908	snp	G/T	1.656e-05	0.00287745	synonymous-codon	HERC1	GRCh38.p7	15:63612424	CCACCTCACGGTACC[G/T]CACCACTTTCTTCAA	8925
rs749264648	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63676700	GGCAGAAGTTGCAGT[A/G]AGCCAAGATCATGCC	8925
rs749281382	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63762151	CAGAAACAATGAAAC[A/G]TATCAGAAAGCAAGG	8925
rs749285824	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63680393	CCTGTTTGTTGTTAA[C/T]AAATGTTTTAAGAAC	8925
rs749295332	in-del	-/T	3.46924e-05	0.00416473	intron-variant	HERC1	GRCh38.p7	15:63674329	CAAAAAAAAAAAAAA[-/T]CAGATAACATACCTT	8925
rs749334127	snp	C/T			utr-variant-3-prime, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63608996	TTCTTATAACATCTA[C/T]GTAGTTACCATAAAA	8925
rs749338896	snp	A/G	3.31296e-05	0.00406985	missense	HERC1	GRCh38.p7	15:63669652	GAGGAGTCTGTGCCC[A/G]ACGTGTGGGAAGTAC	8925
rs749340318	snp	A/G	4.24421e-05	0.00460644	intron-variant	HERC1	GRCh38.p7	15:63662940	TATATGAACAGGAGG[A/G]CAGGAAAATAAGTCA	8925
rs749348319	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63760843	TCACATCTCTAAGAA[C/T]ATCAACCCAGAATGA	8925
rs749350045	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63766890	CCATGTTGGTTCAGG[A/C]TGGTCTGAAACTCCC	8925
rs749350590	snp	A/G	1.69103e-05	0.00290773	synonymous-codon	HERC1	GRCh38.p7	15:63654278	CTGTGAGGACAGCCT[A/G]GAGGAGAGGCAGCAG	8925
rs749355228	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63624485	GCGGATCGCTTGAGC[C/T]CAGGAGTTCAAGACT	8925
rs749373653	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63814457	TGGGTGGGGGAGGGG[A/G]TTGGAGGTTTTTGTT	8925
rs749375577	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63623670	GATCACTGGAAACAG[C/T]AAAATGGCCACTAGC	8925
rs749381689	snp	C/T	1.65759e-05	0.00287883	synonymous-codon	HERC1	GRCh38.p7	15:63628774	TTGCAGACCTGTTAC[C/T]AGGGTTGGTTCTCGA	8925
rs749386130	snp	A/C	1.65756e-05	0.00287881	intron-variant	HERC1	GRCh38.p7	15:63733154	GCATTCTCTAAAGAA[A/C]AATAAAATAGGAACA	8925
rs749386316	snp	A/G	1.72924e-05	0.00294039	intron-variant	HERC1	GRCh38.p7	15:63699020	AAACAGAATAAACAT[A/G]TATCAATGGCAATCA	8925
rs749411078	snp	C/G			missense	HERC1	GRCh38.p7	15:63727785	CAGGGAGTAACAGCA[C/G]GGAGTTAACAATCTG	8925
rs749414005	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63673800	CACAATCTCGGCTCA[C/G]TGTAACCTCCGCCTC	8925
rs749420168	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63712973	AATGGAATTGGAGCA[C/G]AGAGATAATATACAC	8925
rs749432098	snp	A/G	0.000186268	0.00964881	intron-variant	HERC1	GRCh38.p7	15:63755222	TTACATTTTTAAAAA[A/G]TCTTACCTAATCTTC	8925
rs749432687	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63802241	TAAACCACACAAATT[A/G]TCAATGGTTAGCTGT	8925
rs749441688	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63765378	CAGCAACCATCTGAA[G/T]GGACTCCCTCCTATG	8925
rs749464980	snp	A/G	1.65652e-05	0.0028779	missense	HERC1	GRCh38.p7	15:63774860	GAGCCTCGTTGAGCT[A/G]CCAAACCAAGCAGCA	8925
rs749465401	snp	C/T	1.70945e-05	0.00292351	intron-variant	HERC1	GRCh38.p7	15:63637466	AAACCTACATTAGGC[C/T]TTAGGTTCTAACCAT	8925
rs749466555	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63741848	TGATCTATATATTTA[A/T]CCTTCTGACACAGCC	8925
rs749469567	snp	G/T	7.24192e-05	0.006017	intron-variant	HERC1	GRCh38.p7	15:63718549	TTGCAGAAAAACATA[G/T]AAATTAATTGATTTC	8925
rs749473125	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63773578	TTTGAGACAGATTCT[C/T]GCTCTGTTGCCCAGG	8925
rs749473358	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63726640	AAATGGACTTAAGAA[C/G]AAACATAAGATGGAA	8925
rs749513709	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63650286	TGGCACGCGCCTGTA[G/T]TCCCAGCTACCTGGG	8925
rs749526098	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63772046	AGAATCACTTGAACC[C/T]GGGAGGTGGAGGTTG	8925
rs749526420	snp	A/G	6.72427e-05	0.005798	intron-variant	HERC1	GRCh38.p7	15:63689710	ACAATCTGTTTTATT[A/G]AAGAAAAAAGGATAA	8925
rs749555351	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63813205	GATTTGCTAAAGAAT[A/C]TACAGGTGGTTTCTC	8925
rs749555841	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63691339	GGAGTGGTGGTGCAC[A/G]CCTGTGATCCCAGCT	8925
rs749567144	snp	C/T	1.65663e-05	0.002878	synonymous-codon	HERC1	GRCh38.p7	15:63654200	TGTCTGCAGAGTAGT[C/T]TGGTTGTCACGGTCG	8925
rs749574480	snp	C/T	1.76036e-05	0.00296673	intron-variant	HERC1	GRCh38.p7	15:63677815	CCATTAAATATTTGT[C/T]TGCTAAAAGTGTAAC	8925
rs749577931	in-del	-/TT			intron-variant	HERC1	GRCh38.p7	15:63639257	TGTGAAGATGGTCTC[-/TT]AAGATTATAAAACCT	8925
rs749581255	snp	A/G	1.68471e-05	0.00290228	missense	HERC1	GRCh38.p7	15:63659861	TCATTTAAACCAAGC[A/G]GTCCAGCAAGTAATT	8925
rs749589055	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63741081	TCGCCCAGGCTGGAG[C/T]GCAATGGTGCGGTCT	8925
rs749591713	snp	A/G	1.86291e-05	0.00305192	intron-variant	HERC1	GRCh38.p7	15:63680824	AAAAAATCTATTTAT[A/G]TACTATTAACTGCAT	8925
rs749593470	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63825822	CAGGCTGAGTATAGC[A/G]GTGGGTCTCAGCTCA	8925
rs749604135	snp	C/G	3.32149e-05	0.00407509	missense	HERC1	GRCh38.p7	15:63674758	GTTATTTGATGTTGG[C/G]ATTCCACACTTGGCA	8925
rs749611678	in-del	-/TTT			intron-variant	HERC1	GRCh38.p7	15:63695384	TGAGTCTGTATAATC[-/TTT]TTTTTTTTTTTTTTT	8925
rs749614168	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63783775	TCCCCAAAGAATAAA[A/T]CTCATGATCGGGCCG	8925
rs749624815	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63631482	ACTGCACTGCCCTGG[A/C]TCATCAGTGACCTCT	8925
rs749629796	snp	C/T	4.74845e-05	0.00487237	intron-variant	HERC1	GRCh38.p7	15:63764073	ACAAAGTTGTTAATA[C/T]AAAAGCCACGATTAT	8925
rs749639389	snp	C/T	1.74989e-05	0.00295789	intron-variant	HERC1	GRCh38.p7	15:63656389	AACATCTCAGATGGA[C/T]AAAGAAAATGGATTT	8925
rs749644034	snp	A/G	3.43354e-05	0.00414325	intron-variant	HERC1	GRCh38.p7	15:63658533	ATCATGTGACATAAA[A/G]TAACACTTACCTGAC	8925
rs749650101	snp	A/G	3.32414e-05	0.00407671	synonymous-codon	HERC1	GRCh38.p7	15:63640410	GCATTGCATATAGGG[A/G]CTATGAACAAGTTGG	8925
rs749650491	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63690442	TTATGCTATTGAATA[A/G]AAGACACATTTACAA	8925
rs749653629	snp	G/T	2.32577e-05	0.00341003	intron-variant	HERC1	GRCh38.p7	15:63634714	ATCAGCTAGAATATC[G/T]TATTGATTTATTCCA	8925
rs749659030	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63706743	TGAGACAGGGTCTCA[A/C]TAAGATATTTACTAT	8925
rs749666256	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63796534	TGAGTTAGGTCTCAA[C/T]CAATTTAGAAAGTTT	8925
rs749666944	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63686983	AGAGTTCAGTGATTT[-/A]AAGACAAGCAGCATG	8925
rs749705624	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63660599	CTGTCTGTAATCATT[A/G]GGGAATGAGTTATTT	8925
rs749706509	snp	G/T	1.73381e-05	0.00294427	missense	HERC1	GRCh38.p7	15:63634825	GACCATAGTCACCAT[G/T]CCCAAAGGTGAACAG	8925
rs749708623	snp	C/T	1.7127e-05	0.00292629	intron-variant	HERC1	GRCh38.p7	15:63624343	CTGTAACAGAAGGTA[C/T]GGTTATCAGAAATGG	8925
rs749716464	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63779046	AATGAAGAATGAATT[A/T]TAAAAGTGTTCAAGG	8925
rs749735389	snp	A/C/G	9.84138e-05	0.0070142	missense, stop-gained	HERC1	GRCh38.p7	15:63713621	TTCTATCTCGGTCTC[A/C/G]GCTACGAGCTACTTC	8925
rs749736572	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63801183	GAGTTGTATCATTTA[C/T]AATAAACCAGTCATT	8925
rs749738105	snp	A/G	1.82201e-05	0.00301823	intron-variant	HERC1	GRCh38.p7	15:63734694	TTTTAGGATACTACT[A/G]GTTTACTTACACAGC	8925
rs749751762	in-del	-/A	2.01072e-05	0.00317068	intron-variant	HERC1	GRCh38.p7	15:63755216	ATAACTTACATTTTT[-/A]AAAAAATCTTACCTA	8925
rs749752132	in-del	-/C			intron-variant	HERC1	GRCh38.p7	15:63743517	ATCCACCCACCTTGG[-/C]CTCCAAAAGTGCTGG	8925
rs749753041	snp	C/G	6.14685e-05	0.00554351	missense	HERC1	GRCh38.p7	15:63622821	CTGCCATACCTGTCC[C/G]TATTGTAACCCACTT	8925
rs749753656	snp	C/G/T			intron-variant	HERC1	GRCh38.p7	15:63630398	TCCTAGCTTATCTCT[C/G/T]TCCCCAACTGAGGAA	8925
rs749757338	snp	A/G	1.72027e-05	0.00293275	missense, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609124	TTGTCCACGTTTCTC[A/G]AGAGCATGTAGTTGT	8925
rs749773799	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63753218	AAGCTATGTTTCTGA[C/T]AGCTGAGGATGTTAA	8925
rs749781818	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63719113	AGAGCTTATATTATT[C/G]TTAGGAGGAGCAGGG	8925
rs749788929	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63824317	GGTGGGCAGATCACA[A/T]GGTCAGGAGATGGAG	8925
rs749791338	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63673558	GGTACTCAACAAACA[C/T]TGACTGAACGAATCT	8925
rs749808245	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63778502	AAGCAAAAAGGAAGA[C/G]AGAAGCATGCTTTAA	8925
rs749814085	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63765324	CCTTTGGAAAAAGGC[A/G]CAGATCTGTGTAAAC	8925
rs749817540	snp	A/G	1.66413e-05	0.0028845	missense	HERC1	GRCh38.p7	15:63694436	TGGTGTCTGTACCAC[A/G]CAACTGTGACAATAC	8925
rs749819659	snp	A/G	1.65641e-05	0.00287781	missense	HERC1	GRCh38.p7	15:63680644	TCTGTTCTCCATTGT[A/G]ATAGAGGTTACCACT	8925
rs749834674	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63831577	TCATCATTATCATCA[C/T]TTTAAGATCTGAAAA	8925
rs749837025	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63675695	TAGTTTAAGCCAAAA[A/T]ATAATTATATATTTC	8925
rs749859307	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63713762	GTTTGGACCAAAAAC[A/T]TACTGAAAGAGGGAA	8925
rs749859765	snp	A/G	1.81628e-05	0.00301348	intron-variant	HERC1	GRCh38.p7	15:63775658	ATTAGTCCTGCAAAG[A/G]GAGAAGAGAAAACAG	8925
rs749886310	snp	A/G	1.68261e-05	0.00290048	intron-variant	HERC1	GRCh38.p7	15:63680532	TTGTGAATGGGTGTC[A/G]GTACCTCTCCATTTT	8925
rs749890102	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63802957	GCTCATGCCTATAAT[A/C]CCAACACTTCGGGAG	8925
rs749907709	snp	A/C	7.01336e-05	0.00592131	missense	HERC1	GRCh38.p7	15:63775610	AGCTTCACTGGTGGA[A/C]TCATAGTTGCCATGT	8925
rs749914507	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63727104	AACATGGTGAAACCC[C/G]GTCTCTACTAAAAAT	8925
rs749916084	snp	C/G	1.65693e-05	0.00287826	synonymous-codon	HERC1	GRCh38.p7	15:63663044	ATCATTGTCACTGGT[C/G]AGGTCTTGTCCAAAC	8925
rs749922055	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63737938	TTTATGCCTAAACCA[C/T]TCATGAAGATATTCA	8925
rs749928372	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63791074	AGTTTGGAAAATAAA[A/T]AATAAAGTAGGTTTA	8925
rs749946338	snp	A/G	1.65611e-05	0.00287755	synonymous-codon	HERC1	GRCh38.p7	15:63640266	TATAGTGGTTGAGAA[A/G]CATTCTAACCAGGCC	8925
rs749948096	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63623590	ACGTATCACTAACAG[C/T]ATCACTTTATATGAG	8925
rs749953419	snp	C/T	1.65726e-05	0.00287855	synonymous-codon	HERC1	GRCh38.p7	15:63640365	ACACAACAGCTGATC[C/T]AGATGAAGTCCCACA	8925
rs749963271	snp	C/T	1.65721e-05	0.0028785	missense	HERC1	GRCh38.p7	15:63663174	CTCCGACTTTGATTC[C/T]TGTGGGCCTGCACAG	8925
rs749972173	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63760207	GAACAAACTGGAAAA[C/T]GACTTTTTTTTAACA	8925
rs750005781	snp	C/T	8.28054e-05	0.00643396	missense	HERC1	GRCh38.p7	15:63680709	CGGTGATTAAAGTCA[C/T]GTACTGGCCAGCGAG	8925
rs750014652	snp	C/T	3.33417e-05	0.00408286	missense	HERC1	GRCh38.p7	15:63616594	GGTCCAGAGGCTTCT[C/T]TGTGCGAATGGCAAC	8925
rs750021503	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63821867	AACAACATATCCAAG[A/G]TTCCTGCTTTCATGG	8925
rs750027406	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63759376	TGGTAAAGTCTGTTG[C/T]CATTCAAAAGCCTTT	8925
rs750037517	snp	A/G	5.08014e-05	0.00503965	intron-variant	HERC1	GRCh38.p7	15:63755196	CATTTCTAATTTTCT[A/G]GAAGAATAACTTACA	8925
rs750039908	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63637298	TTATTTATATTTCAC[C/T]GAATTCTAGCATTGC	8925
rs750058608	snp	C/G	1.67416e-05	0.00289318	missense	HERC1	GRCh38.p7	15:63698982	TCAGGGATTCCAATT[C/G]ACTGTGCATAGGACC	8925
rs750061330	snp	C/T	1.68066e-05	0.00289879	intron-variant	HERC1	GRCh38.p7	15:63628836	AATAAATCACAAATA[C/T]ACAGACATTCAATTA	8925
rs750074156	snp	A/C	2.79474e-05	0.00373804	missense	HERC1	GRCh38.p7	15:63718683	TCTGATAAGTGTTTA[A/C]CAGGTTGATATCTAA	8925
rs750084939	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63725996	GGGCGGGGGTGGAGG[A/G]GAGCAGACAGAGTCT	8925
rs750107754	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63692036	TCAAGGCAACAGAAA[C/T]CACATTATGATAAGA	8925
rs750109639	snp	C/T	2.76568e-05	0.00371855	intron-variant	HERC1	GRCh38.p7	15:63694300	TTCTACAAAGACATC[C/T]ACCATACTTACCCAG	8925
rs750113831	snp	C/T	1.75167e-05	0.0029594	intron-variant	HERC1	GRCh38.p7	15:63616731	TTTCCTTATTTCTAT[C/T]AGAAATAAGTTAGCA	8925
rs750117700	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63812594	CAGGTTGACAAAAAA[C/T]AAGCAGAATATGAAA	8925
rs750129534	snp	C/T	1.66161e-05	0.00288232	intron-variant	HERC1	GRCh38.p7	15:63733184	AAGTAACTAGCGTAA[C/T]ATGCACTAGAAAAGA	8925
rs750133484	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63649411	TCTACCAATGATTAT[A/G]ACCTTTTTTTCTCTT	8925
rs750141785	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63697749	AGTGAGCCACCGCGC[C/T]CGGCCAATCTTAATC	8925
rs750146493	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63783927	AAAAATTAGCTGGGC[A/G]TGGTAGTGGGCGCCT	8925
rs750147228	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63690655	AGGGATACCTGGAGG[A/G]GAAAAGACCTTTTCT	8925
rs750153375	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63783308	CTTTCAGCAACCCCC[A/C]TCCCGATCAGTCAGC	8925
rs750160905	snp	C/T	1.68046e-05	0.00289862	intron-variant	HERC1	GRCh38.p7	15:63669745	ATCCAATTTACGAAA[C/T]AATACATACATCACA	8925
rs750163202	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63661058	AACATTGCATTTTTA[C/T]ATAAAACAGTTAGTA	8925
rs750177398	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63689157	AAAGCGTTTTGAAAA[C/T]AACAAAAGGCTAGAG	8925
rs750178834	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63825179	CCAGGTGTGGCAGCA[C/T]ACACCCAGCTACTCC	8925
rs750187367	snp	C/T	4.98931e-05	0.00499441	synonymous-codon	HERC1	GRCh38.p7	15:63666092	CTCATGCCCAGGGTG[C/T]TCTATCATCCACATG	8925
rs750190819	snp	A/T	3.31312e-05	0.00406995	missense	HERC1	GRCh38.p7	15:63674905	TCAGGTTTCTGCTCA[A/T]CATCCCCTTTCTCCT	8925
rs750199439	in-del	-/TTT			intron-variant	HERC1	GRCh38.p7	15:63802323	CTATTTAAGAAAGTA[-/TTT]CACTTAGAAAAGGAA	8925
rs750222893	snp	G/T	1.92239e-05	0.00310026	intron-variant	HERC1	GRCh38.p7	15:63752862	TGCCTAAAAATGTAT[G/T]TATTTGAACTTTAAA	8925
rs750240111	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63779832	CATCCTTGCCAACAT[A/G]GTGAAACCCCGTCTT	8925
rs750245728	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63753895	AAAAGATACTCATGC[C/T]GGGCACGGAGGTTCA	8925
rs750249474	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63673879	AAAGGCACACGCCAT[C/T]ATGCCCGGTTAATTT	8925
rs750252028	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63738658	AATAGATAAATTACT[A/G]TAAGTTTCAGAAATA	8925
rs750252200	snp	C/T	5.00856e-05	0.00500403	intron-variant	HERC1	GRCh38.p7	15:63666326	GACTTCTCATATCTG[C/T]ATACACTGATATATA	8925
rs750273206	snp	A/G	3.50656e-05	0.00418707	intron-variant	HERC1	GRCh38.p7	15:63643572	TTCATTATTTTTAAC[A/G]TGCATTAAAATAAAG	8925
rs750286687	snp	A/G	3.64983e-05	0.00427175	synonymous-codon	HERC1	GRCh38.p7	15:63615801	AAGTCGATATTCAAT[A/G]GCCCTCTCCACATAT	8925
rs750289334	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63824206	AATGTAAATTGGAAC[C/T]GCCATTATGGAAAAC	8925
rs750292174	snp	C/T	1.81975e-05	0.00301636	synonymous-codon	HERC1	GRCh38.p7	15:63634772	TGCAGTCACTCTCTC[C/T]GGAAGTTTTTTGTTA	8925
rs750292695	snp	A/G	3.89962e-05	0.0044155	intron-variant	HERC1	GRCh38.p7	15:63758408	ACAAATAGTCAAGAC[A/G]GTTTTAGTCTGGGCA	8925
rs750296725	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63610976	GGAGTCTGGCTAGGT[C/G]TGCCTTCAGCAATGG	8925
rs750298686	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63630026	CCTAAAGATACTTTG[C/T]ATGCCATCATATTAT	8925
rs750302129	snp	A/T	1.81276e-05	0.00301056	missense	HERC1	GRCh38.p7	15:63713605	CCTGCCCCACTGTTC[A/T]TTCTATCTCGGTCTC	8925
rs750302135	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63663293	GCCATACATGTAGGT[A/G]AGAACCTATCTCAGT	8925
rs750342607	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63704873	CCTCCCGAATAGCCA[A/G]GACTACAGGCGCCCA	8925
rs750365232	snp	A/C	1.6563e-05	0.00287771	missense	HERC1	GRCh38.p7	15:63725442	TTGTTCTTTCTAGAT[A/C]CACAAGCCATACCCA	8925
rs750376232	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63806270	CACCCTCAAGCTCCT[A/C]GGCTGAAGCAATCTT	8925
rs750381398	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63673184	AAAAAACCCACTTAG[C/T]TAACAACTCTAAAAG	8925
rs750386617	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63628840	AATCACAAATATACA[C/G]ACATTCAATTAGAAA	8925
rs750391777	snp	A/C	1.65553e-05	0.00287705	intron-variant	HERC1	GRCh38.p7	15:63634901	CATCTAAGACAGAAC[A/C]AAGGAGAAAGAAAAT	8925
rs750396088	snp	C/G	3.17798e-05	0.00398609	intron-variant	HERC1	GRCh38.p7	15:63749625	CAGTTAATACTATTT[C/G]CTTAAAAACAAATGA	8925
rs750402089	snp	C/T	3.28682e-05	0.00405377	intron-variant, splice-acceptor-variant	HERC1	GRCh38.p7	15:63713693	ACACAAAAACAAGGT[C/T]TTAACACATGGGGAG	8925
rs750423923	snp	C/T	1.65839e-05	0.00287953	synonymous-codon	HERC1	GRCh38.p7	15:63674823	TTCTGATTTGGAGCT[C/T]GTGGTACTCTGACTT	8925
rs750473830	snp	C/G	2.02792e-05	0.00318421	missense	HERC1	GRCh38.p7	15:63655898	TGGGTAGAAACTTTC[C/G]CTGAATTGAGTCATC	8925
rs750475334	snp	G/T	1.68562e-05	0.00290307	synonymous-codon	HERC1	GRCh38.p7	15:63712835	TTCACTCCTCGATTT[G/T]ATCAGTCTATAATTT	8925
rs750482966	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63771753	TCTAGTTTTTTAGAG[C/G]CATCTCTGCCCCAAT	8925
rs750488687	snp	C/T	6.62438e-05	0.00575478	synonymous-codon	HERC1	GRCh38.p7	15:63661821	GCAGGTGCCACATAA[C/T]AGGTAGTACGGATTT	8925
rs750491467	in-del	-/TCTG			intron-variant	HERC1	GRCh38.p7	15:63618794	CTCATGATTTGGCTC[-/TCTG]TCTGTTATTGGTGTA	8925
rs750500724	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63804871	GTAGGGAAATGGAAA[C/T]TGAAACCACAACAAG	8925
rs750500826	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63818078	CATGCTAAGCTCTCC[A/T]ATATAATAATTACTC	8925
rs750512574	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63683695	TTTCTGTTACCCAGG[C/T]TGGCATGCAGTAGTG	8925
rs750514112	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63658465	AAAATTCTATCTCAC[C/T]CTCCCAAACACCACC	8925
rs750525196	snp	A/G	9.81499e-05	0.00700466	intron-variant	HERC1	GRCh38.p7	15:63649696	GAAGTTGGAGACTCC[A/G]TCAGCTAGACGTAAG	8925
rs750531719	snp	A/C	1.68596e-05	0.00290336	missense	HERC1	GRCh38.p7	15:63674349	TAACATACCTTGCTT[A/C]ATTTTGCCCCCAAAC	8925
rs750555635	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63816728	TGCCAATCATCCCAG[C/T]ACCAGTGCTGGCATA	8925
rs750557709	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63795304	CATTTATCATTTTGG[A/G]AAAAGAAGTTCAAAG	8925
rs750558891	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63773036	AGCTTTCTACTTGTT[C/G]CGGGTAGGGGGAGAC	8925
rs750565761	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63713288	TTTGGAAACAAACCA[C/T]TTCAGTGCATAAAGT	8925
rs750567510	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63776115	CAGTTCTGATTCCAT[C/T]ATCTGTGTAACAGTG	8925
rs750583465	snp	C/G	3.78766e-05	0.00435165	missense	HERC1	GRCh38.p7	15:63723238	CGGGCAGGCTCTTTA[C/G]AACAACCCAATGCCA	8925
rs750584056	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63711035	GATCTATGTTTCAAA[A/G]TTATTGCAGGGTTGG	8925
rs750593480	snp	A/G	1.66098e-05	0.00288177	missense	HERC1	GRCh38.p7	15:63630603	GTCGATTGTGATTGC[A/G]AGCACGCCCCTCTGG	8925
rs750594195	snp	C/T	3.31857e-05	0.00407329	missense	HERC1	GRCh38.p7	15:63729598	TTTCTGATGATGATG[C/T]TCCAAGTAGAAATTT	8925
rs750594377	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63744502	GACTAGAGTCAAAAA[C/T]CTTAGAGGTCTACCC	8925
rs750613163	in-del	-/AAA			intron-variant	HERC1	GRCh38.p7	15:63611358	CATGGTCAGACAGGT[-/AAA]GCTTAAGAAAGATGA	8925
rs750623082	snp	A/C	3.69624e-05	0.00429882	intron-variant	HERC1	GRCh38.p7	15:63615927	AGGAATCATCTAGGA[A/C]CAGAAGAAAACAGAA	8925
rs750626459	snp	A/T	1.65795e-05	0.00287914	missense	HERC1	GRCh38.p7	15:63638516	TAAGTAGACATCACA[A/T]TTACCTCCCAGGTGC	8925
rs750637455	snp	C/T	6.05089e-05	0.00550007	intron-variant	HERC1	GRCh38.p7	15:63696389	TTAACTCAGACATGA[C/T]GAAACTCTGTATGCC	8925
rs750637770	snp	A/C	1.70784e-05	0.00292214	intron-variant	HERC1	GRCh38.p7	15:63690689	TATCAATGTGACTTA[A/C]ATTCAAAGTTAAAAT	8925
rs750654502	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63757733	TATTTATTTTGAGAC[A/G]GAGCCTCACTCTGTC	8925
rs750660049	snp	G/T	1.68363e-05	0.00290136	missense	HERC1	GRCh38.p7	15:63732952	AAATTTCTTAAGAGG[G/T]TCTTCATCAAAATTT	8925
rs750660579	snp	C/G	1.65781e-05	0.00287902	missense	HERC1	GRCh38.p7	15:63678101	CTTTGCTCTCCTTCT[C/G]CTCTCTCATTTCATT	8925
rs750662350	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63652221	CTAAGTCCAGATACA[A/G]ATGATTTAAAATTAT	8925
rs750672711	snp	C/T	1.65899e-05	0.00288005	intron-variant	HERC1	GRCh38.p7	15:63661060	CATTGCATTTTTATA[C/T]AAAACAGTTAGTACC	8925
rs750679237	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63665489	GCAGTGAGCCGATAT[C/T]GCGCCACTGCACTCC	8925
rs750681591	snp	A/G	1.65636e-05	0.00287776	synonymous-codon	HERC1	GRCh38.p7	15:63630526	TGCCAAAGCAAGTGT[A/G]TGTTCAGCTCCAACT	8925
rs750685108	snp	A/C	1.70191e-05	0.00291706	intron-variant	HERC1	GRCh38.p7	15:63686569	GGTCAGCATTTTGGA[A/C]TAATCCATGTCTCAG	8925
rs750687439	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63800502	ATATCAGTTTAAACA[G/T]TACAGTACCAGAGAT	8925
rs750687610	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63786821	TTTGGAACTAGAGAC[A/G]GTAGTTGCACAATAC	8925
rs750707071	snp	C/T			missense	HERC1	GRCh38.p7	15:63615824	CCACATATTCCTTCC[C/T]GTTGGAAAATGTGAG	8925
rs750707202	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63704802	GGAGTGCAGTGGTGC[A/G]ATCTCGGCTCACTGC	8925
rs750723915	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63785366	TTCAAAGCTGTGAGC[C/T]ATAAGTGCACCACTG	8925
rs750743848	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63828039	TGTTCCGGAATTAGA[C/T]AGTTGTGATGGTTGC	8925
rs750765161	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63677788	ACTGTCGACAGGCAA[C/T]GGCCTATTTCACCAT	8925
rs750767318	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63664230	ATAATTTCTCAAAAT[C/G]TACAAGTGGCCAGTA	8925
rs750782591	in-del	-/CC	1.66521e-05	0.00288544	frameshift-variant	HERC1	GRCh38.p7	15:63616582	GGGCCAAGTGGAGGT[-/CC]AGAGGCTTCTTTGTG	8925
rs750799075	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63634280	TCAAAAAGTATCTAA[C/G]GAATGATATAGAAAA	8925
rs750805252	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63702304	TTGAAATGCACAGAC[-/A]AAATAGCATTTCACC	8925
rs750809461	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63723113	ATTTTCACTTACATA[C/T]ATTGCATATATATTT	8925
rs750810967	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63769705	CTAAAAATATAAAAA[A/T]ATTAGCCAGGCATGG	8925
rs750815786	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63808390	ACTCCTGGGTCCAAG[G/T]GATCCTCCTGCCTCA	8925
rs750825759	snp	C/T	1.65644e-05	0.00287783	synonymous-codon	HERC1	GRCh38.p7	15:63756497	TGAACTATTTCCATG[C/T]CCCAGTTTCCCATAA	8925
rs750831398	snp	A/T	1.6574e-05	0.00287867	missense	HERC1	GRCh38.p7	15:63727779	CTGACACAGGGAGTA[A/T]CAGCAGGGAGTTAAC	8925
rs750836254	snp	C/T	2.11013e-05	0.00324811	missense	HERC1	GRCh38.p7	15:63756721	CATCCGTAGAAATGA[C/T]AAAAGTGCAGTACTG	8925
rs750837391	snp	A/C	2.66244e-05	0.00364849	intron-variant	HERC1	GRCh38.p7	15:63642944	CTATCATTTGATATA[A/C]CTACAATATTACCTT	8925
rs750838347	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63632892	ATGGCATGTATCAAG[A/G]ACTACCTTCCAACAA	8925
rs750853134	snp	A/C	1.6937e-05	0.00291002	intron-variant, missense	HERC1	GRCh38.p7	15:63658726	ATGGCAACCTGAAAA[A/C]CATAATTCTGTTTTG	8925
rs750866019	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63768578	GTGGCTTCGTTATCT[A/C]AAAGCCAACTCTAGT	8925
rs750875968	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63647666	ATGGAATACTATGCA[C/G]CCATAAAAAGAATGA	8925
rs750879036	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63688114	AACAATGGAAGCAGA[C/T]AGAACACTTAGAAGG	8925
rs750889506	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63721862	TTAATTTTCTTTGTT[G/T]TTGTTGCTTGTTTTT	8925
rs750913684	snp	A/C	1.66098e-05	0.00288177	missense	HERC1	GRCh38.p7	15:63623837	AGGTCTGAAGCATTC[A/C]GCTTAACTACTTGTC	8925
rs750913900	snp	C/T	1.66313e-05	0.00288364	intron-variant	HERC1	GRCh38.p7	15:63694709	AAATATAGAACATAA[C/T]TAGTACCATAACCTC	8925
rs750918092	snp	C/T	3.7123e-05	0.00430814	intron-variant	HERC1	GRCh38.p7	15:63623938	AACTCTTACCAATTT[C/T]CCCAAAATCACATGA	8925
rs750955551	snp	A/G	1.67273e-05	0.00289195	stop-gained	HERC1	GRCh38.p7	15:63674471	ACCGCATGACTGCTC[A/G]CTTCACCATGTGTCG	8925
rs750957858	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63658468	ATTCTATCTCACCCT[C/G]CCAAACACCACCAGA	8925
rs750958167	snp	C/T	0.000571793	0.0168988	intron-variant	HERC1	GRCh38.p7	15:63727636	TTTGCTCTTTTATTG[C/T]CTTTACTTACCATGA	8925
rs750960933	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63736588	GAACTTTTAGCATCC[A/C]TCAGTCTTTTAGCAT	8925
rs750961827	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63646338	GGGTGTTCATAATTC[A/G]CTGTTTTAGCTTTAC	8925
rs750962647	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63822315	AAATAGCCAGGTGCT[A/G]TGGCTCACGCCTGCA	8925
rs750964728	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63828165	AGAAGAAAAGGAATA[A/T]AAGAGAACACCCACA	8925
rs750997648	snp	C/T	4.96874e-05	0.0049841	synonymous-codon	HERC1	GRCh38.p7	15:63686440	GTGAGTTAAAATCTG[C/T]CCATTCTCCACTAGG	8925
rs751008462	snp	A/G			upstream-variant-2KB	HERC1	GRCh38.p7	15:63834721	TCCAGCGCCTAACAT[A/G]GGTCCAAGTGGACAT	8925
rs751013810	snp	C/T	0.000299554	0.0122347	missense	HERC1	GRCh38.p7	15:63749787	CCACAGCCCCAAGCA[C/T]AGACCTGAAAAAAAC	8925
rs751034143	snp	A/G	1.73006e-05	0.00294109	intron-variant	HERC1	GRCh38.p7	15:63658528	TTAGCATCATGTGAC[A/G]TAAAATAACACTTAC	8925
rs751036368	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63779844	CATGGTGAAACCCCG[C/T]CTTTAATAAAAATAC	8925
rs751039538	snp	A/G	4.9769e-05	0.00498819	missense	HERC1	GRCh38.p7	15:63664533	TTGTTACCGCTGAGC[A/G]ACCTCTAGCTGATGG	8925
rs751044460	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63657414	GGTTGAACATCTTTT[C/T]ATGTTTATTGGCCAT	8925
rs751067305	snp	A/G			downstream-variant-500B, utr-variant-3-prime	HERC1, FBXL22	GRCh38.p7	15:63608485	ACCCTCAATGTAAAG[A/G]AATGTTTCTGAATGG	8925
rs751076852	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63740479	TCATACAGTAACTCT[A/C]TGTTTAACTATTTAA	8925
rs751089066	snp	A/C	1.65869e-05	0.00287979	missense	HERC1	GRCh38.p7	15:63658626	TCACTCTCCTTAAAG[A/C]CACCACACGGTCATG	8925
rs751089156	snp	A/T	3.6531e-05	0.00427366	missense	HERC1	GRCh38.p7	15:63652416	TGTTAGCACTCACAA[A/T]CTGTTGAACACACAG	8925
rs751094258	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63825124	GAGCAGTCTGGCCAA[C/T]TTGGCAAAACCCCAT	8925
rs751107002	snp	A/C	8.91385e-05	0.00667542	intron-variant	HERC1	GRCh38.p7	15:63641422	CTATAATCACATTCC[A/C]AAGCACCAGGTATCT	8925
rs751124220	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63715561	GTATGCAGAACACAA[A/G]TAAGTTGATAATAAA	8925
rs751128328	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63832856	CTGTTAGGAAATACA[A/C]TAAAATGTTAACCAT	8925
rs751143885	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63748618	GAAGTGGGAAGTTGG[A/G]GATGTAATGCTAATA	8925
rs751147033	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63670135	GAAATTATTCACATG[A/G]ATTGAAAGTAATGGT	8925
rs751161392	snp	A/T	1.66305e-05	0.00288357	intron-variant	HERC1	GRCh38.p7	15:63648240	AGGAAAAGATAATTA[A/T]TTGTCATTGTCTGAC	8925
rs751164366	snp	C/T	5.02559e-05	0.00501253	intron-variant	HERC1	GRCh38.p7	15:63725552	TGTGTCTTTATCTGG[C/T]ACTTTTAAGATTCAA	8925
rs751164660	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63662144	TTCCAACATGTTCAT[C/T]AATGCTAAATAAAAA	8925
rs751165181	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63738927	TACTCACCACCAGGA[-/T]ATTCCTCCAACCCCA	8925
rs751165598	snp	C/T	1.88159e-05	0.00306718	missense	HERC1	GRCh38.p7	15:63734825	ACAGCATGGTTGCTC[C/T]CACTGATAAAGTTTC	8925
rs751169463	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63761854	TTAAAAGGAAGAAGA[C/T]ATAAATGTAAAGGTT	8925
rs751170598	snp	A/G	1.67739e-05	0.00289597	intron-variant	HERC1	GRCh38.p7	15:63713715	CATGGGGAGAGAAGA[A/G]CAAAGAAAATAACAA	8925
rs751177572	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63811810	TGAGACTCCGTCTCC[-/A]AAAAAAAAAAAAAAA	8925
rs751181141	snp	A/C	4.34339e-05	0.00465994	intron-variant	HERC1	GRCh38.p7	15:63622909	GCAGAAGAAAGAAAA[A/C]AATTTTTTGAGAAAT	8925
rs751183490	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63831715	ACATGCTTGGAACGT[C/T]GGAATTGTTATTACT	8925
rs751187419	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63662439	GCAGATTCTCTTTCC[-/T]GTAGGACTTACATCT	8925
rs751202272	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63650010	ACTACTTAATTCTAA[C/T]ACACACTCAAAGCAG	8925
rs751206032	snp	C/T	1.66704e-05	0.00288703	missense	HERC1	GRCh38.p7	15:63694411	AACAACTGCAGGGGC[C/T]GTCCTAGCATGGTGT	8925
rs751209874	snp	C/G	1.68032e-05	0.0028985	missense	HERC1	GRCh38.p7	15:63712816	CAGGCTGAGACAAAT[C/G]AGATTCACTCCTCGA	8925
rs751211518	snp	C/T	1.66087e-05	0.00288168	missense	HERC1	GRCh38.p7	15:63640405	GCCAAGCATTGCATA[C/T]AGGGGCTATGAACAA	8925
rs751232028	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63678925	CTGACACTAATAATA[A/G]CATCTGTCTCCTACA	8925
rs751234871	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63681982	ACGTGTGGAGTCTGA[C/T]GAGTCCTTCTAGTGA	8925
rs751239026	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63802999	AGGCTCACTTGAGCC[C/G]AGGAGTTTGAGACTA	8925
rs751249393	snp	C/G	4.53607e-05	0.00476217	intron-variant, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609297	CAGAGCCGTGACTGG[C/G]GACATCAGAGTGCCA	8925
rs751269951	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63680930	AATAACACGAAAATA[A/C]TCGCATCAATTTAGA	8925
rs751271610	snp	A/G	1.66715e-05	0.00288712	intron-variant	HERC1	GRCh38.p7	15:63680791	ACTAAAATAAAAGTG[A/G]GATATTCATTAATAC	8925
rs751282128	snp	A/G	1.67217e-05	0.00289147	intron-variant	HERC1	GRCh38.p7	15:63663219	GCTCAGAACAAAACA[A/G]AAAAGGCATTTTATT	8925
rs751284428	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63650748	TAAGGCTAGCTATTC[A/C]TCAAATGTCACACAG	8925
rs751286706	in-del	-/AGATA	6.9081e-05	0.00587671	intron-variant	HERC1	GRCh38.p7	15:63686583	AATAATCCATGTCTC[-/AGATA]AGATATATTCTGAGG	8925
rs751289233	snp	A/G	1.65619e-05	0.00287762	synonymous-codon	HERC1	GRCh38.p7	15:63725458	CACAAGCCATACCCA[A/G]GACTGAGCTGGCTGA	8925
rs751292014	in-del	-/G	2.78408e-05	0.0037309	intron-variant	HERC1	GRCh38.p7	15:63712939	TTTTGATTTAGGACT[-/G]TTAGTGAACATAAAA	8925
rs751292562	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63773226	GGTGGGCAGATCACC[A/T]GAGGTCAGGAGTTCC	8925
rs751295958	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63682752	TTGCTAGAGGTTTGA[C/G]TAAACTTAAGATGTG	8925
rs751296241	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63774203	AGAAATTTTCACTAC[C/T]TGAAATTATATATTT	8925
rs751300383	snp	A/G	0.000100981	0.00710493	intron-variant	HERC1	GRCh38.p7	15:63692582	CTACAGTGAAGAGAC[A/G]AGTTTACGTTACAAC	8925
rs751325821	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63676165	CCTCTGCCTCCCAAA[C/T]TGCCGGGATTACAAG	8925
rs751327877	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63760348	ACAGAAAAGTATTGA[C/G]GTCAAATCCCATATG	8925
rs751335490	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63664030	TACTAATGTAATGAG[A/G]GAATCTGGTCCTTAT	8925
rs751356861	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63726121	CAAGTAGCTGGGAGT[A/G]TAGGTGTGCACCACG	8925
rs751364256	snp	A/C	2.60007e-05	0.00360551	intron-variant	HERC1	GRCh38.p7	15:63645439	AGATAACAGTCTATA[A/C]CAATATAAAAACTAA	8925
rs751368051	snp	C/T	1.65605e-05	0.0028775	missense	HERC1	GRCh38.p7	15:63645029	CACCATCCTTCTGCA[C/T]TAGTCACATTGGTCT	8925
rs751372707	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63637431	GCAAAGGTTTGAGAA[C/G]GGCAAAGGTTTGTAC	8925
rs751374799	snp	A/T	1.67382e-05	0.00289289	intron-variant	HERC1	GRCh38.p7	15:63666498	AGGAAGAGAAATAAG[A/T]ACCTAAATATCACTA	8925
rs751374888	snp	A/G	1.69706e-05	0.0029129	intron-variant	HERC1	GRCh38.p7	15:63661713	CTTAAGGTATGAGGT[A/G]TCTTCAGGAGGTCTG	8925
rs751397526	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63813871	TCAGGAGTTTGAGAC[C/G]AGCCTGGTGAAACCC	8925
rs751400113	snp	A/T	1.66288e-05	0.00288343	missense	HERC1	GRCh38.p7	15:63732964	AGGGTCTTCATCAAA[A/T]TTTCAGCCAGGTGGG	8925
rs751401096	snp	C/T			upstream-variant-2KB	HERC1	GRCh38.p7	15:63835490	CTCACAAATATGATA[C/T]TCTGTCTTTCTTGAA	8925
rs751411027	snp	G/T	3.51636e-05	0.00419292	synonymous-codon	HERC1	GRCh38.p7	15:63626084	CACCGTGTGAATGCT[G/T]ACTTCTCTCAGCGCC	8925
rs751413391	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63784363	GAGCAATCTCCAAGA[C/T]ACACTGTTAAAAAAG	8925
rs751421229	snp	C/T	1.85451e-05	0.00304503	missense	HERC1	GRCh38.p7	15:63696287	GAGATGCTACCTTTT[C/T]CTTCCATCCCAGACA	8925
rs751422762	snp	C/T	1.65674e-05	0.00287809	synonymous-codon	HERC1	GRCh38.p7	15:63638726	CTCAGGTCTGGAAGT[C/T]GCCCAAGACATAATT	8925
rs751428803	snp	C/G/T	8.7057e-05	0.00659714	missense	HERC1	GRCh38.p7	15:63652510	CTTGTAGCCAAAAGA[C/G/T]CTTTTTTATTACACC	8925
rs751431404	in-del	-/AG			intron-variant	HERC1	GRCh38.p7	15:63811036	ATTTGGGAAAAAAAA[-/AG]GCTGGGGTTTACTCT	8925
rs751434502	snp	C/T	1.88745e-05	0.00307195	intron-variant	HERC1	GRCh38.p7	15:63752874	TATTTATTTGAACTT[C/T]AAAATTTAAATACAA	8925
rs751437181	snp	A/G	1.66349e-05	0.00288395	synonymous-codon	HERC1	GRCh38.p7	15:63616439	ATTTACCTCATGGAA[A/G]CTCTCCTCGGTAATC	8925
rs751447743	snp	C/T	4.48873e-05	0.00473726	intron-variant	HERC1	GRCh38.p7	15:63774662	TTCCAAAAACTATTA[C/T]GAACTTTAAAGTTGA	8925
rs751450575	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63812814	AAATTATTAAGGAAA[G/T]AAATCAAAGATAATC	8925
rs751452621	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63826564	TACTATGAATCAATG[C/T]AGCACTTCCATTAAA	8925
rs751459128	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63646498	GCAATAGTAGAGGCT[-/A]AAAAAAAAAAAAAAC	8925
rs751489074	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63612242	GGAAAAAAGAATAGC[-/T]TTACTTACCCTATCA	8925
rs751492788	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63689509	AGAGCAAGGTGCCTC[A/G]GAGGAACAGGCATTC	8925
rs751500636	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63740576	TTTCTCCACCTCCTC[C/T]AATGTTTGCTATTAG	8925
rs751512478	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63797235	TTCTGCTAAGGTGTA[A/G]GCATAGTTTCTATCA	8925
rs751516933	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63661285	TAACCAAATTCTATT[C/G]CATAAAGCCTTAAAG	8925
rs751520545	snp	C/T	1.65842e-05	0.00287955	missense	HERC1	GRCh38.p7	15:63753010	CCAGCACAAACTTTG[C/T]GAATGAACATTCCTT	8925
rs751527113	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63783367	ATGAGCAAAAAGATT[A/C]CAACTCTTTGAAGGA	8925
rs751529066	snp	A/G	1.71708e-05	0.00293003	missense	HERC1	GRCh38.p7	15:63626151	TGCAGAGGTACTGAC[A/G]CACCTGTCCAGAAAG	8925
rs751537577	snp	A/G	2.16097e-05	0.003287	intron-variant	HERC1	GRCh38.p7	15:63698704	TTCCAGAGCTCTCAT[A/G]AGGAGTAAATATCAA	8925
rs751541442	snp	C/T	1.67562e-05	0.00289444	synonymous-codon	HERC1	GRCh38.p7	15:63729626	TTTATCACTATTCTT[C/T]TCTAGCTCTCCAAAT	8925
rs751553855	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63754059	CATGCCTGTAGTCCC[A/T]GCTACTTGGGGGGCT	8925
rs751562058	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63631178	TCTAAAATGAGAGAT[C/T]ATTCAACTTGTCTTG	8925
rs751582149	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63825512	TATACAATAAATAAG[A/T]AAGTAAGCCTGAAAT	8925
rs751584731	snp	G/T	9.95322e-05	0.00705381	synonymous-codon	HERC1	GRCh38.p7	15:63675030	AGAAGCCGTCAGGCC[G/T]CGGAATCGCGCCACA	8925
rs751586314	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63673977	TGATCTGCCCACCTC[A/G]GCCTCCCAAAGTGCT	8925
rs751591460	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63694934	TTTTCTATTAGCAAC[A/G]ATAATACCTGCTTGC	8925
rs751594632	snp	C/G	5.03952e-05	0.00501947	missense	HERC1	GRCh38.p7	15:63674483	CTCGCTTCACCATGT[C/G]TCGCATCAAGAACTG	8925
rs751597402	snp	C/T	1.65789e-05	0.0028791	synonymous-codon	HERC1	GRCh38.p7	15:63713397	ACTTGTTGAAGGTTG[C/T]TGCAACTGTCCTTCT	8925
rs751601627	snp	C/T			missense	HERC1	GRCh38.p7	15:63718584	TTTACCCATCTGTCC[C/T]GTGATGATGACCTTG	8925
rs751610362	snp	A/T	1.66098e-05	0.00288177	intron-variant	HERC1	GRCh38.p7	15:63666343	TACACTGATATATAA[A/T]AACTTATCCTACCTG	8925
rs751611702	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63720059	AGTTGAAAACCGAAA[C/T]CACAACATTAGATGA	8925
rs751637944	snp	C/T	8.03762e-05	0.0063389	intron-variant	HERC1	GRCh38.p7	15:63756766	ATAAACAAAGAATCA[C/T]AAATATAAAATACTT	8925
rs751644353	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63806997	GTGATCCACCCACCT[C/T]GGCCTCCCAAAGTGC	8925
rs751650325	snp	C/G	1.79142e-05	0.00299279	missense	HERC1	GRCh38.p7	15:63656178	ATAGGCCAGGCAAGA[C/G]ATAGGCTTGTTAGCC	8925
rs751650504	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63644572	GAATTTATGTTACTC[A/G]CCTAGAGGGCTCTCT	8925
rs751660522	snp	A/C/T	3.45121e-05	0.00415392	intron-variant	HERC1	GRCh38.p7	15:63665901	CATGGAACAAAAGTA[A/C/T]AGAAACTGGAATTTC	8925
rs751666603	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63733405	CATACTATGCATAAT[A/G]ATTTTAGTACTGTAA	8925
rs751666988	in-del	-/CTG			intron-variant	HERC1	GRCh38.p7	15:63742342	TTTTACCCTGAAGCT[-/CTG]CTGAACTCGTTTATT	8925
rs751673430	snp	C/T	0.000109858	0.00741059	intron-variant	HERC1	GRCh38.p7	15:63656073	TAACGGGGAAAAGTA[C/T]TGAAAGTAGCTTACC	8925
rs751677663	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63643308	ATTCAAGAGATTACT[A/G]TATAAAATGTTTCTA	8925
rs751680392	snp	C/T	8.00256e-05	0.00632506	missense	HERC1	GRCh38.p7	15:63641600	GTTGCCAAAACATGA[C/T]TGGCAGCTGCCCATT	8925
rs751695686	snp	A/G	1.70006e-05	0.00291548	intron-variant	HERC1	GRCh38.p7	15:63640125	AAAATCTCAGCTGCA[A/G]ATAATAGCAGCTCAC	8925
rs751699276	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63819458	AGACAGTTTGCTTAA[C/T]CTTGCTCCTTAATAT	8925
rs751712762	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63766029	CCTAAATTGATTTGC[A/G]ACCTGTCTCAGATAG	8925
rs751716194	snp	C/T	9.88289e-05	0.00702885	missense	HERC1	GRCh38.p7	15:63694032	TCTTCACCGTCTTCT[C/T]GCTCCCCTTCTCCGA	8925
rs751720475	snp	C/T	7.48615e-05	0.00611761	synonymous-codon	HERC1	GRCh38.p7	15:63723252	AGAACAACCCAATGC[C/T]AAGTCTACATAGACA	8925
rs751745649	snp	C/T	0.000122466	0.00782421	intron-variant	HERC1	GRCh38.p7	15:63624110	TAGTAATAACATCCA[C/T]CTGAAAAAATCACAG	8925
rs751764507	snp	A/T	1.6643e-05	0.00288465	synonymous-codon	HERC1	GRCh38.p7	15:63678240	AGTCCAACGGTCTGT[A/T]CGGTGAAGGATACGG	8925
rs751765722	snp	A/G	1.66515e-05	0.00288539	missense	HERC1	GRCh38.p7	15:63775392	GAAGGGCATCCAAAT[A/G]GTGGTCCTGCTCATC	8925
rs751767761	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63764861	ATAAGATCTCAGGAG[C/T]TGGGTGAGTGGGATC	8925
rs751792559	snp	A/G	6.74627e-05	0.00580748	synonymous-codon	HERC1	GRCh38.p7	15:63630630	CTGGCAAGCCTATCA[A/G]GCGATCTGAAAAAAA	8925
rs751817282	snp	A/G	3.68983e-05	0.00429509	intron-variant	HERC1	GRCh38.p7	15:63678385	ATAAAAGTAAAGAGG[A/G]TGGAAAACACATGCT	8925
rs751828620	snp	C/T	7.1673e-05	0.00598593	intron-variant	HERC1	GRCh38.p7	15:63675151	TGACACAGGAAGAAG[C/T]AAGTGAGGGAAAGAC	8925
rs751833400	snp	A/G	8.86407e-05	0.00665676	intron-variant	HERC1	GRCh38.p7	15:63632692	TACCCAAGCAAATAA[A/G]CTGAAAAATGTCTTA	8925
rs751836694	snp	C/T	4.99247e-05	0.00499598	missense	HERC1	GRCh38.p7	15:63659840	GGTTCTGGTACAATG[C/T]GCCGGTCATTTAAAC	8925
rs751845469	snp	C/T	1.66499e-05	0.00288525	synonymous-codon	HERC1	GRCh38.p7	15:63623854	CTTAACTACTTGTCT[C/T]GCTATTTGGACAAAA	8925
rs751846953	snp	A/G	1.65693e-05	0.00287826	missense	HERC1	GRCh38.p7	15:63774837	TCCATTCAAGAAGAT[A/G]TCGCAATGAGCCTCG	8925
rs751857539	snp	A/G			intron-variant, missense	HERC1	GRCh38.p7	15:63654343	CAGCAGAAGGATCAT[A/G]GGAAGGATGGGCATA	8925
rs751868704	in-del	-/A	3.34882e-05	0.00409182	intron-variant	HERC1	GRCh38.p7	15:63651400	ATATAACAGACAGAT[-/A]ATGCAGTTCTAATCC	8925
rs751881338	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63697750	GTGAGCCACCGCGCC[C/T]GGCCAATCTTAATCA	8925
rs751886412	snp	C/T	1.65627e-05	0.00287769	missense	HERC1	GRCh38.p7	15:63669619	CATCAGAAGGAGAGG[C/T]TGGTAACGAAGATAT	8925
rs751923694	in-del	-/A	1.67427e-05	0.00289328	intron-variant	HERC1	GRCh38.p7	15:63638397	TCTTTTCTATTTTTT[-/A]TCCTGTTAGTTACCT	8925
rs751929057	snp	A/T	1.75339e-05	0.00296085	intron-variant	HERC1	GRCh38.p7	15:63690528	ATCTTCTAATAATTT[A/T]AAAAATAAAAACCTG	8925
rs751940901	snp	C/T	3.31285e-05	0.00406978	synonymous-codon	HERC1	GRCh38.p7	15:63654158	GATAAAGGAGCATTT[C/T]CTAAGATCTCCTCCC	8925
rs751943507	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63616282	TAAACTGCTGCGGTT[C/G]AGCTGCTAAGGGCAG	8925
rs751947309	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63653325	GTGTACATCTGTAAT[A/C]CCAGCTATGCGGGAG	8925
rs751947376	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63666895	TCTGCCTTCATGTTT[C/G]AGCTCTCATGTGAAA	8925
rs751950399	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63744696	TAAGGCCCAGGGATT[C/T]TTAAGTTAGCTTATG	8925
rs751952576	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63759151	CTCAGAAATGGGACT[C/T]GGAATTCAAAAAAAG	8925
rs751962149	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63707928	GCAAGACTCCCTCTC[-/A]AAAAAAAAAAAAAAA	8925
rs751963196	snp	C/G	1.65666e-05	0.00287802	missense	HERC1	GRCh38.p7	15:63677903	TGCTGCCCTCTTTGA[C/G]CACTCCCAGCAGCGT	8925
rs751972833	snp	C/G	5.00363e-05	0.00500156	missense	HERC1	GRCh38.p7	15:63718603	ATGATGACCTTGTTT[C/G]AATAAGTTCAAGGTT	8925
rs751994406	snp	A/G	1.65817e-05	0.00287933	synonymous-codon	HERC1	GRCh38.p7	15:63654236	AGCAAGAGTGCGCAC[A/G]AGTTGCTGAGCTGCC	8925
rs752007482	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63757859	GGACTACAGGCATGC[A/G]CCACCATGCCTGGCT	8925
rs752007792	snp	A/C	1.65762e-05	0.00287886	missense	HERC1	GRCh38.p7	15:63727794	ACAGCAGGGAGTTAA[A/C]AATCTGGCAGAGCAT	8925
rs752022073	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63829032	ATGAAAGCCAGGTTT[C/T]TGACAGAGACAGAAG	8925
rs752025542	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63648883	CCATGTAAGCAGGCA[C/T]TATGACTTTGAATTA	8925
rs752026131	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63679430	GGAAATATTATACAT[C/G]ATAAAACCTGAAAGC	8925
rs752027933	snp	C/T	3.31263e-05	0.00406965	missense	HERC1	GRCh38.p7	15:63774975	AGCAGTCCAAGCCCA[C/T]AGGAGGAATCTTGCT	8925
rs752041399	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63811094	AGCAATATATGAATG[C/T]GATTGGATCCTGGAC	8925
rs752058423	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63683067	CTTGAAACTGGCAGG[G/T]GGAGGTTGCAGGGAG	8925
rs752059475	in-del	-/AAAC			intron-variant	HERC1	GRCh38.p7	15:63779177	AGGAAGAAAAATACA[-/AAAC]AAACAAAAACAGAGC	8925
rs752069555	snp	A/G	0.000186515	0.00965519	intron-variant	HERC1	GRCh38.p7	15:63637080	TACAGTGGTTTCTCC[A/G]AAGGTGTTCTCTCTC	8925
rs752073704	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63811400	TGCAATTTGTGAATC[A/T]AGGTGAAAAGCGCTA	8925
rs752075074	snp	G/T	1.65611e-05	0.00287755	missense	HERC1	GRCh38.p7	15:63612490	TCTGCTCCAGTTGTT[G/T]TGCTGTGAGGAGGGA	8925
rs752079854	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63634600	ACAGTTAAAATTATC[A/C]ATTAGACCATAGCAA	8925
rs752080004	snp	C/T	1.65754e-05	0.00287879	missense	HERC1	GRCh38.p7	15:63624255	GCAGAGTGTAGACTC[C/T]TGGGGCTAACAAAGG	8925
rs752095996	snp	C/T	1.98454e-05	0.00314997	intron-variant	HERC1	GRCh38.p7	15:63716497	AATTATCAGAAACTA[C/T]ACTAAATACATTTTT	8925
rs752096021	snp	A/G	4.73115e-05	0.00486349	intron-variant	HERC1	GRCh38.p7	15:63729205	TACTTCTTAATGACT[A/G]ATTAAATTTGAAATG	8925
rs752107110	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63689395	AGATAAAAATGTGAT[C/T]TAGGAGAGAGGAAAT	8925
rs752108505	snp	G/T	1.66029e-05	0.00288117	missense	HERC1	GRCh38.p7	15:63694836	AACTGTTGATAAATT[G/T]TATGCACAGCTACCT	8925
rs752110832	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63724081	AACAAAATAAAATTT[C/T]AATAGTTTCATGATT	8925
rs752129867	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63782248	AGAAATAATTCAATA[C/T]CTGCCTTCAAAGGAC	8925
rs752131365	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63808809	AGAGGAATGAAGATC[C/G]TGAGGGTCCTTATCA	8925
rs752152010	snp	C/T	1.68738e-05	0.00290458	intron-variant	HERC1	GRCh38.p7	15:63666511	AGAACCTAAATATCA[C/T]TAGATACCGTGAGTA	8925
rs752164713	snp	C/G	1.72116e-05	0.00293351	intron-variant	HERC1	GRCh38.p7	15:63658741	ACATAATTCTGTTTT[C/G]TTCTCAACAAGGTAA	8925
rs752174820	snp	A/G	1.65674e-05	0.00287809	missense	HERC1	GRCh38.p7	15:63654138	TTCTGATGAGCCTCC[A/G]ATTTGATAAAGGAGC	8925
rs752198158	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63810231	ACCAATGTTAATAGG[A/G]GCATTATTCATAATA	8925
rs752204616	snp	C/T	1.74955e-05	0.00295761	missense	HERC1	GRCh38.p7	15:63716471	GTCCTGGTTTTCTGA[C/T]ATCTTAAAGAAATTA	8925
rs752211764	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63676680	AGAATTGCTTGAACC[C/T]GGGAGGCAGAAGTTG	8925
rs752218946	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63633159	GCTTTTATGGGCGAC[A/C]ATAACTGCTTTATAT	8925
rs752219737	snp	A/T	1.65888e-05	0.00287996	missense	HERC1	GRCh38.p7	15:63753016	CAAACTTTGCGAATG[A/T]ACATTCCTTGTAAAG	8925
rs752224312	snp	C/T	3.11687e-05	0.00394758	missense	HERC1	GRCh38.p7	15:63652519	AAAAGACCTTTTTTA[C/T]TACACCAAACACATG	8925
rs752231060	snp	G/T	3.31208e-05	0.00406931	missense	HERC1	GRCh38.p7	15:63645048	TCACATTGGTCTGTG[G/T]AGTATCTTGAGGAAT	8925
rs752232602	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63768749	AACTTGGGTTTAAAT[A/C]TAGGCTCCATCCCTT	8925
rs752266027	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63610668	AAGCCTAGCCCAGGA[A/G]CAGAGCAGCAGCCTG	8925
rs752278060	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63827536	GTGCAAAAGAGTATA[G/T]TATACTCTCCACATA	8925
rs752297149	snp	C/G/T	0.000304365	0.0123326	missense	HERC1	GRCh38.p7	15:63727757	TAACTCAATAAAGGC[C/G/T]GAGCCACTGACACAG	8925
rs752305949	snp	C/T	3.31813e-05	0.00407302	synonymous-codon	HERC1	GRCh38.p7	15:63658648	ACGGTCATGAGGGTT[C/T]GCTAGGGCAGCTGCC	8925
rs752318645	snp	A/G			intron-variant, missense	HERC1	GRCh38.p7	15:63702203	AAAAGGAGTAAATAC[A/G]CTACCACACGAGAAT	8925
rs752320738	snp	C/T	1.65792e-05	0.00287912	missense	HERC1	GRCh38.p7	15:63612354	AGCACCCGCTCCTCA[C/T]TGGAGAACTCTTCCA	8925
rs752332019	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63748879	ACCTGATGGACTAAA[C/T]ACGTACAGTTAGCAC	8925
rs752344402	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63715844	ATTCTTGCTCCCTAT[A/C]GAAACAGCAGTGTAG	8925
rs752348026	snp	C/T	1.67556e-05	0.0028944	intron-variant	HERC1	GRCh38.p7	15:63635914	AAACCTATTCAACAA[C/T]TAGTATATTTACAAT	8925
rs752350833	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63628314	GCAGTCATTTGAACC[C/T]GGGAGGCGGAGGCTG	8925
rs752356123	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63609804	CTCACATAAGGAAGG[C/G]GCAGTCAATTAAACT	8925
rs752367639	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63825477	ATGTATATCAAAACA[C/T]CATGTGTACACATTA	8925
rs752379647	snp	A/G	1.68607e-05	0.00290346	intron-variant	HERC1	GRCh38.p7	15:63725562	TCTGGTACTTTTAAG[A/G]TTCAAAATATTTCTC	8925
rs752383115	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63670233	GAATGATATGTCAGC[C/G]GCACAGTCGGGGAAA	8925
rs752385730	snp	A/G	3.33289e-05	0.00408207	intron-variant	HERC1	GRCh38.p7	15:63694705	CACAAAATATAGAAC[A/G]TAACTAGTACCATAA	8925
rs752398916	snp	C/T	1.73706e-05	0.00294703	synonymous-codon	HERC1	GRCh38.p7	15:63626096	GCTGACTTCTCTCAG[C/T]GCCCCATACTGGGGG	8925
rs752399133	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63671086	CACATGCCTGTAATC[A/C]CAACTACTCAGGAGG	8925
rs752401247	snp	A/C	1.65611e-05	0.00287755	synonymous-codon	HERC1	GRCh38.p7	15:63636006	GATCTGCCTGGGCCG[A/C]CGCTGCCTGTCGCTG	8925
rs752426149	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63640019	ACTATCTGAAAGAAA[A/C]ATATTTTCCATTTCT	8925
rs752438439	in-del	-/AATT	7.16872e-05	0.00598652	intron-variant	HERC1	GRCh38.p7	15:63718551	GCAGAAAAACATAGA[-/AATT]AATTGATTTCAAACT	8925
rs752448725	snp	C/T	5.56726e-05	0.00527572	intron-variant	HERC1	GRCh38.p7	15:63680509	TAGAAACAAGAAAAA[C/T]GTAATGCTTGTGAAT	8925
rs752455176	snp	A/G	4.97649e-05	0.00498798	missense	HERC1	GRCh38.p7	15:63658635	TTAAAGCCACCACAC[A/G]GTCATGAGGGTTTGC	8925
rs752462047	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63795803	TCCACTGGCTGGAAC[A/G]GGACCTGACATTCTG	8925
rs752473671	snp	A/T	1.99364e-05	0.00315718	utr-variant-3-prime, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609071	AGGGAGGGTGAGAGC[A/T]CCCGCACGGTCAGTA	8925
rs752475065	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63814986	ATAAAATGAGTGGGG[A/T]CCTAAATGAGTTCCA	8925
rs752500359	snp	A/G	1.71167e-05	0.00292542	intron-variant	HERC1	GRCh38.p7	15:63680027	ACTCTATCTGATGCT[A/G]AACAATAAAATAACA	8925
rs752504161	snp	C/T	1.65916e-05	0.00288019	missense	HERC1	GRCh38.p7	15:63775424	CTTGAAAGAGACTCA[C/T]GTTCAAAGTCTGGCA	8925
rs752504847	snp	A/G	1.72442e-05	0.00293629	synonymous-codon	HERC1	GRCh38.p7	15:63674520	TGCTCGCATCTCCAC[A/G]TCTTCATGAACAACT	8925
rs752505216	snp	A/G	9.66791e-05	0.00695199	intron-variant	HERC1	GRCh38.p7	15:63694266	ATTCTAAAATGGAGG[A/G]AGACCAGACTTCATA	8925
rs752513096	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63775754	TCAAACTGGTGAAAT[A/G]CAGCCGGGTGCGGTG	8925
rs752516298	in-del	-/CA	0.0426437	0.139654	intron-variant	HERC1	GRCh38.p7	15:63747682	GCACACACGCGCGCG[-/CA]CACACACACACACAA	8925
rs752526583	in-del	-/ATC			intron-variant	HERC1	GRCh38.p7	15:63707571	ACTTGACATTATGGT[-/ATC]AGCAATTTCAATTGT	8925
rs752535629	snp	A/T	1.65649e-05	0.00287788	missense	HERC1	GRCh38.p7	15:63640228	GGAAACTGGGCTCCA[A/T]TGGTCAGGGCTTCGG	8925
rs752542720	snp	A/G	3.31912e-05	0.00407363	synonymous-codon	HERC1	GRCh38.p7	15:63616451	GAAACTCTCCTCGGT[A/G]ATCCCACTGTCTTCA	8925
rs752565245	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63742824	GTCATGGGGTACAAT[C/T]TTTTAGGTAAGTTGC	8925
rs752574397	snp	C/T	1.65767e-05	0.00287891	missense	HERC1	GRCh38.p7	15:63732983	CAGCCAGGTGGGTAT[C/T]TGGATGGCAGCTCTG	8925
rs752578978	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63803132	ATCGCTTAAGCCTAC[A/G]AGGCTGCAGTGAGCC	8925
rs752585991	snp	C/G	7.44075e-05	0.00609904	missense	HERC1	GRCh38.p7	15:63632786	GCAACCTTTTTTATT[C/G]CAATTCCACAAAGGA	8925
rs752595576	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63827842	ACATGCTACAACATG[G/T]ATGAACCTTGACAAA	8925
rs752600574	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63818704	AACCAAAGTATTTCA[A/T]ACTATTCTCAAAAGA	8925
rs752625051	snp	A/C	1.71513e-05	0.00292837	intron-variant	HERC1	GRCh38.p7	15:63754467	TTAAAAAACTCAAGA[A/C]AAAAGCCAAAGCTAC	8925
rs752632607	snp	A/G	0.000132463	0.00813721	synonymous-codon	HERC1	GRCh38.p7	15:63661854	ACTCCCACATTCACC[A/G]CCAAACCAGCCATCC	8925
rs752658258	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63651112	ATTTGAAGCACACAG[C/T]GCATAGATTGAAATT	8925
rs752662390	snp	A/C	7.54973e-05	0.00614353	missense	HERC1	GRCh38.p7	15:63723266	CCAAGTCTACATAGA[A/C]AGCAATTTCAGGCCG	8925
rs752664415	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63664040	ATGAGGGAATCTGGT[C/T]CTTATCTAGCAGTGA	8925
rs752666760	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63693536	GTTGTGAGCCACTGC[A/G]CCTGGCCTGGGGGAC	8925
rs752669781	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63727433	CAAGGTCATCTTTCC[A/T]ACTCCAATGCTTTTC	8925
rs752692968	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63785459	TCAATTCAAAATTAG[A/G]AAAACAAAATAAACT	8925
rs752696737	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63666613	TGTGGCTGGGCACTG[C/T]GGCTCACACCTGTAA	8925
rs752698421	snp	C/G	1.65976e-05	0.00288072	missense	HERC1	GRCh38.p7	15:63616534	GGTCCTCTAGGGTGA[C/G]TGGGACACAGCACAG	8925
rs752713954	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63812371	TAACATGACTGGAGG[-/T]TAAGTTTTAGCAGGG	8925
rs752722787	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63741711	TTCTTTTGCATGTGG[G/T]TATACAGTTGTCCAA	8925
rs752729331	snp	C/T	7.91264e-05	0.00628943	missense	HERC1	GRCh38.p7	15:63694045	CTTGCTCCCCTTCTC[C/T]GAAAGAGGCCATATG	8925
rs752737460	snp	G/T	1.65699e-05	0.00287831	synonymous-codon	HERC1	GRCh38.p7	15:63669551	ACCTGTGCGGTTAGC[G/T]GGCCTTGCTGACTGG	8925
rs752746184	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63784469	AATAAATGCTGAAAA[C/G]ATTTTTTTAAAACCT	8925
rs752755964	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63663331	TTGGATCTCAGACCA[C/T]AAAACATCAAATTAT	8925
rs752757091	snp	G/T	0.000186306	0.00964979	intron-variant	HERC1	GRCh38.p7	15:63637122	GAACTCTGATGAAGA[G/T]GTCCTTTAAAGTCTT	8925
rs752757765	snp	A/G	2.52733e-05	0.00355471	intron-variant	HERC1	GRCh38.p7	15:63696110	ATCTGTATATACTGC[A/G]AGGTGTCACCTACCT	8925
rs752784135	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63708920	AATCTGCTTTCTCTC[C/T]AGTTCTTGTCTTTTC	8925
rs752799476	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63787243	TTCACTGCAACCTCC[A/G]CCTCCAGGATTCAAG	8925
rs752805265	snp	C/T	1.65693e-05	0.00287826	missense	HERC1	GRCh38.p7	15:63666046	CAGGCCTAGAGTCTG[C/T]TGTGCTGCCCGACTG	8925
rs752809954	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63632238	TCACATATCCCTAAA[A/C]AACTACCCTTGCCAA	8925
rs752816445	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63797347	CATGTGGCCAAGGGT[C/T]ACAATATTTGTCACT	8925
rs752822516	snp	C/T	1.67638e-05	0.0028951	intron-variant	HERC1	GRCh38.p7	15:63633983	CACCTAAAGAAATAA[C/T]AGCATTCCGTAAGGC	8925
rs752824148	snp	A/G	1.66765e-05	0.00288756	missense	HERC1	GRCh38.p7	15:63651324	CTGATACTCCAGGAA[A/G]CTGGTGAGAAACTTG	8925
rs752837164	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63659491	CTGCTGGCCTCAAGC[A/G]ACCTTCTTTCTTCAG	8925
rs752837906	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63661442	TTAAAATGCCAGAAA[C/T]ATGGTAGAAAATACA	8925
rs752846736	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63754975	AGGATCATGATGGTA[C/T]TGCTTTTATCCCAGA	8925
rs752851964	snp	A/C/G	4.99865e-05	0.00499912	missense	HERC1	GRCh38.p7	15:63659844	CTGGTACAATGCGCC[A/C/G]GTCATTTAAACCAAG	8925
rs752858053	snp	C/T	2.006e-05	0.00316695	intron-variant	HERC1	GRCh38.p7	15:63643395	TAAAAATAAAATCTA[C/T]GCTCTTACCCTTAAA	8925
rs752861543	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63720314	ACCAGTATTGTACTT[C/T]AACAATGTAGTATAT	8925
rs752862077	snp	C/T	2.16946e-05	0.00329345	intron-variant	HERC1	GRCh38.p7	15:63729227	TTTGAAATGAAATAC[C/T]AAACTCACCTCTTAA	8925
rs752867170	snp	A/G	1.6734e-05	0.00289253	synonymous-codon	HERC1	GRCh38.p7	15:63749534	CCAGGCATAAACTTC[A/G]TTATCTAAAAACAAA	8925
rs752871809	snp	C/T	1.65787e-05	0.00287907	missense	HERC1	GRCh38.p7	15:63624261	TGTAGACTCTTGGGG[C/T]TAACAAAGGCCGAAG	8925
rs752872511	snp	A/G			missense	HERC1	GRCh38.p7	15:63747794	TCTCAAGAAAAGAAC[A/G]CAGGTGTGAGAAGGT	8925
rs752873931	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63807204	CTCAAATCAAGCCTA[C/T]TCTCTACCCTTCAAG	8925
rs752877656	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63687229	CTAATCAGGATATCC[C/T]TGCAAGTTCAGGTAA	8925
rs752886124	snp	C/T	5.01157e-05	0.00500553	missense	HERC1	GRCh38.p7	15:63694849	TTTTATGCACAGCTA[C/T]CTGGATTTCAATCTG	8925
rs752889427	snp	G/T	1.77884e-05	0.00298226	intron-variant	HERC1	GRCh38.p7	15:63612585	AGGTTGCTCATTCAA[G/T]GAGTGTGCGTGAACC	8925
rs752895886	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63631343	CTGCACTGAAATTCT[A/C]CTCTCAAAAGCCATG	8925
rs752899774	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63767496	TCTGAGGTCAGGAGT[C/T]AGAGACCAGCCTGAC	8925
rs752906693	in-del	-/TGTGTG			intron-variant	HERC1	GRCh38.p7	15:63829543	GTGCACATATATGTA[-/TGTGTG]TGTGTGTGTGTGTGT	8925
rs752909833	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63754140	GTTTGCATCACTGCA[C/T]TCTAGCCTGGGTAAC	8925
rs752913960	snp	C/G	1.69095e-05	0.00290765	intron-variant	HERC1	GRCh38.p7	15:63651214	GAAGGCTTTAAAAAA[C/G]TACTTTCAGCAGTTT	8925
rs752918464	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63779669	GATTACAATAGGCTT[A/G]TAAATGTATAAATGT	8925
rs752921375	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63808243	ATGATTCTGAATAAC[A/G]GCTGCTATCAAACTT	8925
rs752923188	snp	C/G	1.73794e-05	0.00294778	intron-variant	HERC1	GRCh38.p7	15:63624135	TCACAGCTCATTAGT[C/G]AAACACACATACATA	8925
rs752934872	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63679002	GTACATTGCCAGTCA[C/T]ACTGTAAATGTTAAA	8925
rs752966585	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63733546	ATCTAAACTAATGCA[A/G]AATACTCATTAAAAA	8925
rs752982098	snp	C/T	2.31881e-05	0.00340493	intron-variant	HERC1	GRCh38.p7	15:63755206	TTTCTAGAAGAATAA[C/T]TTACATTTTTAAAAA	8925
rs752996562	snp	C/T	9.73568e-05	0.00697631	intron-variant	HERC1	GRCh38.p7	15:63655703	TTAAAAATAAGAAGT[C/T]GATTAGAAGACTGTA	8925
rs753001304	snp	A/C	9.96066e-05	0.00705644	intron-variant	HERC1	GRCh38.p7	15:63706875	AATTTAGTTGTGAAA[A/C]GTATTTTAAGATTAA	8925
rs753036174	snp	C/T	1.65644e-05	0.00287783	synonymous-codon	HERC1	GRCh38.p7	15:63775081	GAGACCAGGTCCTGA[C/T]ACAGGCATCATCCAA	8925
rs753036522	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63766412	GGCCAACATGGTAAA[A/C]CCTTGTCTCTACTAA	8925
rs753056746	snp	C/T			missense	HERC1	GRCh38.p7	15:63638463	ACCATTACATTTCTT[C/T]CAGCTTCTGCCAGCT	8925
rs753063952	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63654473	GAATTGGCACTTTTG[C/G]AAGCAATTATTTCAC	8925
rs753072870	in-del	-/C	1.65954e-05	0.00288053	frameshift-variant	HERC1	GRCh38.p7	15:63666462	AGTCTACTGCTTGGG[-/C]TCTGACAAGGCTGAG	8925
rs753073941	snp	C/T	1.8239e-05	0.0030198	intron-variant	HERC1	GRCh38.p7	15:63734674	ATTTCCTTCTCAGTC[C/T]AAATTTTTAGGATAC	8925
rs753093396	snp	A/G	0.00027533	0.0117299	synonymous-codon	HERC1	GRCh38.p7	15:63746993	ACCTGCCTGCCTCCC[A/G]AGAATGCTGGTAGCT	8925
rs753106385	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63819578	CTTACACCAATTACT[A/G]TTCTCTTCTAACATC	8925
rs753107374	snp	C/T	0.000138066	0.00830745	synonymous-codon	HERC1	GRCh38.p7	15:63672612	GCTCATAAAGGAGGT[C/T]GTGCTTGAGGCTGAT	8925
rs753113798	in-del	-/TTGT			intron-variant	HERC1	GRCh38.p7	15:63831098	TGTAGACCTTTGTTG[-/TTGT]TTGTTTTGTTTTATT	8925
rs753116590	in-del	-/ATATATAC			intron-variant	HERC1	GRCh38.p7	15:63829494	AATATATATATATAT[-/ATATATAC]ACACACACACATATA	8925
rs753117945	snp	C/T	1.6574e-05	0.00287867	missense	HERC1	GRCh38.p7	15:63630498	TCCCCCAGGCATACA[C/T]ATCTCCATTTGATGC	8925
rs753149845	snp	C/T	2.0013e-05	0.00316324	intron-variant	HERC1	GRCh38.p7	15:63718722	CCAAAATAGAAAAGT[C/T]ACCTAATTTCTGACA	8925
rs753151712	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63666985	GTCGGTGATTTCCCT[G/T]ATTAAAATGGCCCCA	8925
rs753157342	snp	A/G	7.59446e-05	0.0061617	missense	HERC1	GRCh38.p7	15:63648091	GCATCAATTAGAACA[A/G]TGCCTCCTTTCTCAA	8925
rs753158999	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63623521	TAAGAACTGATATTT[A/G]TGTAGTAAGGTATCT	8925
rs753161209	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63699126	TGTTTGAATACGCGC[A/G]TGCATTAAGTGAATC	8925
rs753161290	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63818635	ATTCCTTTATATGGC[A/G]TAGCTTTGAGAGTTT	8925
rs753161951	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63788658	ACAGTGGCTCATGCC[C/T]GCAATCCCAGCACTT	8925
rs753166671	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63668185	ATTTAAAACCAACCA[C/T]ATCAATGATCACATT	8925
rs753174482	snp	A/G	1.71696e-05	0.00292993	intron-variant	HERC1	GRCh38.p7	15:63755343	GCATTGCACACAAGT[A/G]AATACGATGAGTATG	8925
rs753177921	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63640920	ATCCTGGTAGCCATC[-/A]AAGGAAAAGCAAAAA	8925
rs753182476	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63809792	TGTTTAGAATAGCAA[-/A]AAAAAAAAAAAAAGT	8925
rs753186773	snp	A/G	1.66452e-05	0.00288484	missense	HERC1	GRCh38.p7	15:63654259	GAGCTGCCCATTGCC[A/G]ATGCTGTGAGGACAG	8925
rs753188832	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63760128	AAAAAAATTGAACTG[C/G]ATAGGGACAACAGAA	8925
rs753192394	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63637070	CGGGGGCTTGTACAG[C/T]GGTTTCTCCAAAGGT	8925
rs753205955	snp	C/T	1.68923e-05	0.00290618	intron-variant	HERC1	GRCh38.p7	15:63628850	ATACAGACATTCAAT[C/T]AGAAAGAGGAAGAGA	8925
rs753210876	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63759286	AGCGAAGGCACAAAG[A/C]AATTAACATTCACAC	8925
rs753211294	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63790854	AAAAACAAAAAAAGT[C/T]TGTATGACCATATTG	8925
rs753211813	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63609907	AAGGTGTTCAGGATA[C/T]ATTAGGAGGTTAAAG	8925
rs753218903	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63697498	TCACTCTTGTTGCCC[A/G]GGCTGGAGTGCAATG	8925
rs753220134	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63801781	ATATATCCTAGGGAT[A/T]CTATCTGCAGTCCAC	8925
rs753224887	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63712242	AAGGCTTCTGCACAC[A/G]TCCACTCAAAAGAGA	8925
rs753230662	snp	C/T	3.59008e-05	0.00423664	intron-variant	HERC1	GRCh38.p7	15:63615764	CCGAGATGTTTCATC[C/T]CACCTGTCTGTCCAT	8925
rs753239537	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63725822	TTACCCAGACCAAAA[C/T]TCACTATCTTTAGGG	8925
rs753239698	in-del	-/ATAA			intron-variant	HERC1	GRCh38.p7	15:63643945	ACATGCTGACTCTAT[-/ATAA]ATAGATTCCTCTTTT	8925
rs753240535	snp	C/G			synonymous-codon	HERC1	GRCh38.p7	15:63727762	CAATAAAGGCCGAGC[C/G]ACTGACACAGGGAGT	8925
rs753256525	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63640941	AAAGCAAAAAGCTGG[A/C]AGACAGGCTACTTTA	8925
rs753264028	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63771224	AGAAACACGGGTTCT[A/G]GAGACCAAAAACATC	8925
rs753266212	in-del	-/A	0.00424823	0.0458919	intron-variant	HERC1	GRCh38.p7	15:63672703	CAATCTCTAGAAACC[-/A]AAAAAAAAGGTTAAG	8925
rs753267313	in-del	-/A	0.000134925	0.00821246	intron-variant, frameshift-variant	HERC1	GRCh38.p7	15:63654360	GAAGGATGGGCATAC[-/A]ATTGGGCAATTAAAC	8925
rs753284286	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63830349	TTAACCTCAATCAAA[C/T]CATGAGAAAAAACAT	8925
rs753292764	snp	C/T	1.65721e-05	0.0028785	synonymous-codon	HERC1	GRCh38.p7	15:63661986	ACACAGTTCACACAC[C/T]ACCACTTCTTCCCTG	8925
rs753297781	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63679605	AGGTGAAAGAGAAAG[C/T]TTACAATGGAGGGTA	8925
rs753297795	snp	A/C	1.65616e-05	0.00287759	missense	HERC1	GRCh38.p7	15:63669600	CTTTGCCTCCTTCCT[A/C]CTTCATCAGAAGGAG	8925
rs753300186	snp	A/C	1.65641e-05	0.00287781	missense	HERC1	GRCh38.p7	15:63677921	CTCCCAGCAGCGTGG[A/C]ATGGCGCCCAGTTTG	8925
rs753327705	snp	A/G	1.65603e-05	0.00287747	missense	HERC1	GRCh38.p7	15:63733051	GTACACACAGAAGAT[A/G]GGTCAGCAGCATCAG	8925
rs753328934	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63812318	TTTCAAAACAGTAGG[A/C]ATTCCTATGTTAGAA	8925
rs753336453	snp	A/C/T	6.02305e-05	0.00548747	synonymous-codon	HERC1	GRCh38.p7	15:63694061	GAAAGAGGCCATATG[A/C/T]AGTACACCAGTTTGG	8925
rs753337873	snp	C/G	1.78023e-05	0.00298343	missense	HERC1	GRCh38.p7	15:63645574	GGCAGAGTGAATGTA[C/G]ACAGCACCAGCATCC	8925
rs753345282	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63800770	GATAGGGGAATAGGA[C/G]CATCTTTTGTTATTC	8925
rs753384043	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63811536	TGAAAGGGGCCGGGC[A/G]CGGTGGCTCACGCCT	8925
rs753386310	snp	A/C	1.65952e-05	0.00288051	missense	HERC1	GRCh38.p7	15:63640163	TTACCATTAGAAATA[A/C]AAGTTCATCCTCTGG	8925
rs753388373	snp	G/T			missense	HERC1	GRCh38.p7	15:63678212	TTTCCATCATTTTTT[G/T]GTTAATGCAGTAAGT	8925
rs753411021	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63801300	TAGGCAATTCAGAAG[-/T]GTGGGACTCAATACA	8925
rs753438680	snp	C/T	1.66891e-05	0.00288864	intron-variant	HERC1	GRCh38.p7	15:63754685	AACAAAGAAACAACA[C/T]TAACTCTTTTTCTCT	8925
rs753441944	snp	C/G	0.000101792	0.0071334	missense	HERC1	GRCh38.p7	15:63718599	CGTGATGATGACCTT[C/G]TTTGAATAAGTTCAA	8925
rs753451725	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63783098	TTAGAATATTACATA[A/C]ATTTAATTGATAATG	8925
rs753460479	snp	A/C	7.90733e-05	0.00628732	missense	HERC1	GRCh38.p7	15:63648081	TACCTTATGTGCATC[A/C]ATTAGAACAATGCCT	8925
rs753469341	snp	A/C	1.66297e-05	0.0028835	synonymous-codon	HERC1	GRCh38.p7	15:63616562	CAGCTGCTTCCACAC[A/C]AGAGGGGCCAAGTGG	8925
rs753470470	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63610922	TGCAGTAAGTTCTGG[A/G]TTTGAGGGCTGTACC	8925
rs753471485	snp	A/C	1.65822e-05	0.00287938	synonymous-codon	HERC1	GRCh38.p7	15:63774793	CTCCATGGTGTGTAC[A/C]ACTGCCGAAGCCCCC	8925
rs753474295	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63689493	AAATGGAATAAATGA[C/T]AGAGCAAGGTGCCTC	8925
rs753474642	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63736911	CACGCCCGGCCATAG[C/T]ATCACACTCTTACCC	8925
rs753489626	snp	G/T	5.04834e-05	0.00502386	intron-variant	HERC1	GRCh38.p7	15:63636188	ACTGGATGTTAAAAC[G/T]CTCCTCTTTACTTGC	8925
rs753498140	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63783246	CCAATCAATGCAGCA[A/G]ACTTCACTGTTGTCT	8925
rs753504344	snp	A/G	1.77046e-05	0.00297523	intron-variant	HERC1	GRCh38.p7	15:63626186	TGGGCACTTATGAAG[A/G]AAACAGCATTGCTTT	8925
rs753509534	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63822859	AAGATGATTTGCTAA[C/T]AGACTGGTTAAAGGG	8925
rs753514241	snp	A/C	0.000100852	0.00710042	missense	HERC1	GRCh38.p7	15:63689659	GCAATGGGTGTCTCC[A/C]ACATACAATCAGAGA	8925
rs753518306	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63738536	AATATTTCCTTAAGT[C/G]TACAGGTAGTTCAAA	8925
rs753520353	snp	A/C	7.59633e-05	0.00616246	intron-variant	HERC1	GRCh38.p7	15:63716488	TCTTAAAGAAATTAT[A/C]AGAAACTACACTAAA	8925
rs753527323	snp	C/G	1.78261e-05	0.00298542	intron-variant	HERC1	GRCh38.p7	15:63675143	GATCAGAATGACACA[C/G]GAAGAAGCAAGTGAG	8925
rs753531533	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63752094	CATAGTGAGAAACAC[A/G]TAGAAGAGATATTCT	8925
rs753537767	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63704327	TTCTTTTATTCCAAA[A/G]ATATTATTTTGTACA	8925
rs753546743	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63823944	AAGGAACTCACACAA[C/T]GCAATAGCAAAAAAC	8925
rs753548011	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63800137	ACCTAGTCTCTTAAG[-/A]AAAAAAAGAAGAAGA	8925
rs753552985	snp	A/T	1.65674e-05	0.00287809	synonymous-codon	HERC1	GRCh38.p7	15:63698899	GGTAAGATCAAAATC[A/T]GACTCAAAGGAATAG	8925
rs753568023	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63719765	TCTGTGATGTGAGAA[C/T]ATGAGAGAAGTCAAA	8925
rs753574859	snp	G/T	1.73724e-05	0.00294719	missense	HERC1	GRCh38.p7	15:63713593	CGAGCCCCAGACCCT[G/T]CCCCACTGTTCATTC	8925
rs753578517	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63814843	TATGAAACCTACCTG[A/T]CTACGTCTCAAAATT	8925
rs753599659	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63750215	GATTATATAAATCAC[A/G]AAACTGATGTTTATT	8925
rs753601014	snp	G/T			upstream-variant-2KB	HERC1	GRCh38.p7	15:63835895	GACCAATCAAGAGAC[G/T]CCCTCTTTTACCATC	8925
rs753608533	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63633305	TTGTAAATCACACTG[C/G]TTGTGAAATACGTCA	8925
rs753617184	snp	C/T			synonymous-codon	HERC1	GRCh38.p7	15:63624190	TACAGTTATCTGAGG[C/T]CCATAGTTTTTGCCT	8925
rs753630355	snp	C/T			upstream-variant-2KB	HERC1	GRCh38.p7	15:63834815	CAGCCACCTTCATGG[C/T]GTCTTTCCTTCCAGA	8925
rs753631931	snp	C/G			missense	HERC1	GRCh38.p7	15:63698768	ATTGCAATGATGGAG[C/G]CCTGGGGACTTGTAG	8925
rs753637823	snp	A/G	1.69798e-05	0.00291369	synonymous-codon	HERC1	GRCh38.p7	15:63656349	AGCAGCCAGGCTACA[A/G]CTGGAACCACTGCCA	8925
rs753638765	snp	A/T	2.49038e-05	0.00352864	intron-variant	HERC1	GRCh38.p7	15:63758382	AACCTATTAAAAATT[A/T]AAAATATGCAACAAA	8925
rs753648940	snp	C/T	1.65663e-05	0.002878	synonymous-codon	HERC1	GRCh38.p7	15:63758229	CAGTATTTTCTCCTG[C/T]GTACCTTCTACCAAC	8925
rs753658633	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63794586	GCACACAAAAAGACA[C/G]AGATCACTTTGGAGA	8925
rs753666872	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63658755	TGTTCTCAACAAGGT[A/G]AGAAAAAAATACATC	8925
rs753681582	snp	C/G	1.6569e-05	0.00287824	missense	HERC1	GRCh38.p7	15:63666010	CATTTGACTTCCCGC[C/G]ACTGCCTAGAACGGC	8925
rs753703275	snp	A/G	2.22408e-05	0.00333465	intron-variant	HERC1	GRCh38.p7	15:63725261	GGTACAAACAGGCAT[A/G]TATTTTAAATGCTGC	8925
rs753709716	snp	G/T	6.668e-05	0.0057737	synonymous-codon	HERC1	GRCh38.p7	15:63651347	GAAACTTGGATCACT[G/T]GGTGATCCCAGGCTT	8925
rs753722310	snp	A/G	1.65877e-05	0.00287986	missense	HERC1	GRCh38.p7	15:63624269	CTTGGGGCTAACAAA[A/G]GCCGAAGTTGTCCCT	8925
rs753729588	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63816576	TACTCTAAGTCACAA[A/G]CTATTTATTTCATGA	8925
rs753750533	snp	A/G	1.66266e-05	0.00288323	synonymous-codon	HERC1	GRCh38.p7	15:63749395	GAGCAGTCCATGCCA[A/G]ACTATGTGATGTTCC	8925
rs753756678	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63671550	CACAAGACCACAGCA[A/G]TAATTCTCAAAGTGT	8925
rs753757312	in-del	-/CGCGCACA			intron-variant	HERC1	GRCh38.p7	15:63833750	AAGCACACACGCGCG[-/CGCGCACA]CACACACACACACAC	8925
rs753765312	snp	C/T	1.72698e-05	0.00293847	missense	HERC1	GRCh38.p7	15:63775593	AGTGTTCAAGCCATT[C/T]CAGCTTCACTGGTGG	8925
rs753766374	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63734430	CAACAGTAGCACATA[C/T]ACTTGATTTCAACTC	8925
rs753780877	snp	A/C/G	1.7653e-05	0.00297089	missense, stop-gained	HERC1	GRCh38.p7	15:63656210	TGCTATGCCCACCTC[A/C/G]TGATCGTTCTGAGGT	8925
rs753794788	snp	A/T	1.65669e-05	0.00287805	missense	HERC1	GRCh38.p7	15:63640215	GGTAAAAGATTCTGG[A/T]AACTGGGCTCCATTG	8925
rs753796441	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63653057	ATCTGAGACCTATTA[C/T]AATCTTTACTAAATA	8925
rs753806318	snp	A/G	1.70304e-05	0.00291803	intron-variant	HERC1	GRCh38.p7	15:63616698	CTGTAAAATTAAAGG[A/G]AATATTTCAAACAGC	8925
rs753815483	snp	C/T	3.31763e-05	0.00407272	synonymous-codon	HERC1	GRCh38.p7	15:63725338	ACTGAACAGTGGCGT[C/T]TTCATCCAATATGCA	8925
rs753816516	snp	C/T	3.03642e-05	0.0038963	intron-variant	HERC1	GRCh38.p7	15:63694288	GACTTCATACAGTTC[C/T]ACAAAGACATCTACC	8925
rs753823897	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63804024	AAAGTGTCAAGGCAG[G/T]TTAATAGGAAAAGGA	8925
rs753827265	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63646608	AATTCGAGACCAGCC[C/T]GGCCAGCATGGTGAA	8925
rs753833505	in-del	-/T	1.67513e-05	0.00289402	intron-variant	HERC1	GRCh38.p7	15:63752926	TCCTCTGAAATACTC[-/T]TAAGTCTTTTATACT	8925
rs753855504	snp	C/T	1.72665e-05	0.00293819	missense, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609172	CAGTTGTTGATGGCA[C/T]AGCGCAGGCGCTCGG	8925
rs753860051	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63610876	AGAGTGGGGATGGAG[-/A]ACAGAGGGAGGAGAG	8925
rs753867735	snp	A/G	3.50865e-05	0.00418832	intron-variant	HERC1	GRCh38.p7	15:63680519	AAAAATGTAATGCTT[A/G]TGAATGGGTGTCGGT	8925
rs753870661	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63775838	AGGCCAGGAGTTCAA[C/G]ACGAGCCTGGCCAAC	8925
rs753879729	snp	C/T	1.65658e-05	0.00287795	missense	HERC1	GRCh38.p7	15:63729549	TGTTTCTGTAGTGAA[C/T]ATAGCAGTTCATGAA	8925
rs753879780	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63744236	TGGGGGTGGAGTGAC[A/G]CAAGCACCCCTGTGG	8925
rs753882489	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63652029	CAGCAGAGCGAGACT[C/T]AGTCTCAAAAAAGAA	8925
rs753894593	snp	C/T	1.69e-05	0.00290684	intron-variant	HERC1	GRCh38.p7	15:63660927	GTTAAGCAGAGAGGA[C/T]ATATAAAAAAACATG	8925
rs753915775	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63696061	ACCAAAAAGTTTCAC[A/G]TTATTAAAGTGGCTT	8925
rs753915793	snp	A/C	1.68513e-05	0.00290265	intron-variant	HERC1	GRCh38.p7	15:63690669	GGGAAAAGACCTTTT[A/C]TTATTATCAATGTGA	8925
rs753920870	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63632850	CACAACTTTAAGAAG[-/A]AAAAAAATCACTCTT	8925
rs753926140	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63664148	CTTACCACTGATGCT[A/G]AACATTAAACATGCA	8925
rs753945402	snp	G/T	8.50883e-05	0.00652203	intron-variant	HERC1	GRCh38.p7	15:63749597	TCAAATGTAATATAT[G/T]TACACAAGACAACAG	8925
rs753945421	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63756307	GTAAACTGTAAAGCA[C/G]AGATACAAAAGATTA	8925
rs753955323	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63785796	GAAGGAAGGAAAAGG[A/G]GAAGGGGAAGGGAAG	8925
rs753958110	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63615661	ACATACATACAGAGG[A/C]ATTAACACAGTAAAT	8925
rs753962075	snp	C/T	3.35773e-05	0.00409726	intron-variant	HERC1	GRCh38.p7	15:63643561	CCATCCTGAAATTCA[C/T]TATTTTTAACATGCA	8925
rs753965372	snp	C/T	1.65781e-05	0.00287902	missense	HERC1	GRCh38.p7	15:63678065	CGAGGCCATGCCTAG[C/T]ATGTTTACCTTTCTC	8925
rs753966781	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63827911	ATATTATATGATCCA[A/T]TAACACAAAACATCC	8925
rs753972310	in-del	-/AT	1.69458e-05	0.00291078	intron-variant	HERC1	GRCh38.p7	15:63616410	AACACCAGTAGAAAC[-/AT]AGACTGGCCAGGATT	8925
rs753978228	snp	C/T	8.05315e-05	0.00634502	intron-variant	HERC1	GRCh38.p7	15:63625917	GGCCCTGGGGCCTGG[C/T]GAGCATGTCACGGGC	8925
rs753998470	snp	C/T	3.59926e-05	0.00424205	intron-variant	HERC1	GRCh38.p7	15:63718736	TTACCTAATTTCTGA[C/T]ATCATGAGAGCAAAT	8925
rs754005436	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63742921	TGCATCAGAGTACTT[C/T]AATAGCTGGTCTATA	8925
rs754008798	in-del	-/AC			intron-variant	HERC1	GRCh38.p7	15:63815670	CTGTAGTGAAGTCAA[-/AC]ACACTCTTCATGGTT	8925
rs754011428	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63676323	TCTTAGCTTGGTAGA[A/C]TGGAGGGGAAGGCAG	8925
rs754019947	snp	A/G	1.65655e-05	0.00287793	missense	HERC1	GRCh38.p7	15:63729552	TTCTGTAGTGAACAT[A/G]GCAGTTCATGAAGAT	8925
rs754046648	snp	C/T	1.84059e-05	0.00303358	intron-variant	HERC1	GRCh38.p7	15:63652381	TTAGGATTCTCTTAT[C/T]TTAAATGGTATACAC	8925
rs754050475	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63614794	AATGCTTACTTACCT[A/G]TCAGCACAGAACAAG	8925
rs754059098	snp	A/G	2.33092e-05	0.0034138	synonymous-codon	HERC1	GRCh38.p7	15:63713649	TTCACGGGCTGAGAG[A/G]AAACACTGAAAGATT	8925
rs754059137	snp	A/G	1.99874e-05	0.00316122	missense	HERC1	GRCh38.p7	15:63696132	CACCTACCTGATAGT[A/G]ATGCAATCGGCCACT	8925
rs754061001	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63799312	TTGAGACCAGCCTGG[A/G]AAATATGGCAAAACC	8925
rs754070542	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63768369	CCAGTGCTATTGTCT[G/T]TGGCTCACACTTTGA	8925
rs754106281	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63726156	CTGGCTAATTTTTGT[A/G]TTTTTAGTAGAGATG	8925
rs754152116	snp	C/T	2.48352e-05	0.00352377	intron-variant	HERC1	GRCh38.p7	15:63649685	AGTCTAGAAAGGAAG[C/T]TGGAGACTCCGTCAG	8925
rs754181853	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63804815	AAAGATACATAAACA[G/T]CCAAAAAAGCGCATG	8925
rs754186438	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63675555	TTGGTCAGATGTAGT[C/T]TGATGTAAGCTATTC	8925
rs754191273	snp	A/G	1.77181e-05	0.00297636	intron-variant	HERC1	GRCh38.p7	15:63641440	GCACCAGGTATCTGT[A/G]TATCTCTAGGAGTGA	8925
rs754206130	snp	A/G	1.72003e-05	0.00293255	intron-variant	HERC1	GRCh38.p7	15:63674333	AAAAAAAAAAATCAG[A/G]TAACATACCTTGCTT	8925
rs754208466	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63720635	ATTGACAAGGACAAA[C/T]ATGCCAGATTTTAAG	8925
rs754230650	snp	A/T	5.03546e-05	0.00501744	intron-variant	HERC1	GRCh38.p7	15:63663231	ACAAAAAAGGCATTT[A/T]ATTTGCATGCATAAA	8925
rs754240261	snp	C/T			missense	HERC1	GRCh38.p7	15:63645063	TAGTATCTTGAGGAA[C/T]GCGCCAAACACATAC	8925
rs754241910	snp	A/C			stop-gained	HERC1	GRCh38.p7	15:63655767	AACTTCTGACTTATC[A/C]TAGTTAGGTCTTAGT	8925
rs754248820	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63631634	AACCTCTGCCTTCCA[G/T]GTTCAAGCAATTCTC	8925
rs754259144	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63771350	AAATTCAATCTAATG[C/T]AGGCCTGAGGTGGCT	8925
rs754261043	snp	A/G	1.65888e-05	0.00287996	missense	HERC1	GRCh38.p7	15:63664530	TTCTTGTTACCGCTG[A/G]GCGACCTCTAGCTGA	8925
rs754262669	snp	C/G			downstream-variant-500B, stop-gained	HERC1, FBXL22	GRCh38.p7	15:63608248	GGCCAGATGGCATTA[C/G]TGTGGTCCTCTTCCT	8925
rs754266353	snp	C/T	7.01041e-05	0.00592006	missense	HERC1	GRCh38.p7	15:63746992	GACCTGCCTGCCTCC[C/T]GAGAATGCTGGTAGC	8925
rs754271901	snp	C/T	4.67082e-05	0.00483238	intron-variant, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609303	CGTGACTGGGGACAT[C/T]AGAGTGCCATAAGGG	8925
rs754280170	snp	A/G	1.72701e-05	0.0029385	intron-variant	HERC1	GRCh38.p7	15:63755349	CACACAAGTAAATAC[A/G]ATGAGTATGCACATG	8925
rs754280235	snp	A/G	3.31763e-05	0.00407272	missense	HERC1	GRCh38.p7	15:63775223	CCAGAACTGCTCTCC[A/G]GAGAATGCTGCTGCT	8925
rs754291066	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63733759	CAGAAGGCTGAGGTG[C/G]GAGAATCACTTGAGC	8925
rs754295843	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63687298	TAATCCCAGCAATTT[G/T]AGAGACCGAAGCGGG	8925
rs754298548	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63779797	GAGGTGGGAGGATCA[C/T]GAGGTCAAGAGATGG	8925
rs754313144	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63825539	AAATAAACAAATAAA[A/G]TGAGAGAGAAGAGAC	8925
rs754317649	snp	G/T	1.65897e-05	0.00288003	missense	HERC1	GRCh38.p7	15:63630594	TTTGTTGCGGTCGAT[G/T]GTGATTGCGAGCACG	8925
rs754342172	snp	C/T	1.66167e-05	0.00288237	missense	HERC1	GRCh38.p7	15:63678190	CATATCTTAATTTTG[C/T]GAAGCCTTTCCATCA	8925
rs754343884	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63652620	GTTGTATCCAATTTT[C/T]AAAAATCTACCATGA	8925
rs754353523	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63792234	ATCTTGGGCAAGAAC[A/G]CATACCCTCTTCTCC	8925
rs754356507	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63625154	CACGCACACACAATA[A/G]CTAGCCACTTTGTTA	8925
rs754361771	snp	C/T	1.65745e-05	0.00287871	synonymous-codon	HERC1	GRCh38.p7	15:63756545	GAAGACTTCTCCTTC[C/T]GTCGTAAAGGCTAAA	8925
rs754385714	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63700520	TAGGATTTCAAAATT[C/T]GTAACACGGAGCTAA	8925
rs754391692	snp	C/T	0.000180031	0.00948594	intron-variant	HERC1	GRCh38.p7	15:63718943	AAAGGGCTCAGAAAA[C/T]AGTTCAGAGGTAATT	8925
rs754401268	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63832762	CAAGCAGGCCAGAGA[A/G]CTGATTCAAATAAAA	8925
rs754413826	snp	C/T	5.44529e-05	0.00521761	intron-variant	HERC1	GRCh38.p7	15:63625947	CACTGCTTACCAAGC[C/T]AGTCTGTGCCTGGCT	8925
rs754416212	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63819737	ATGACAATACTTGGA[C/T]GGGGTTTTCTATCAG	8925
rs754424910	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63767698	AGCGAGGCTCCGTCT[C/T]AAAAACAAAACAAAA	8925
rs754431884	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63679898	AACATGAAATAGTGC[A/C]TTAATATTAATATAT	8925
rs754438012	in-del	-/TT	4.85402e-05	0.00492623	intron-variant	HERC1	GRCh38.p7	15:63678402	GGAAAACACATGCTA[-/TT]AGTAGTTCTTCTTAG	8925
rs754454591	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63687493	CAGTAAGCAGAAATC[A/G]CGCCACTGCACTCCA	8925
rs754461598	snp	C/G	3.79197e-05	0.00435413	missense	HERC1	GRCh38.p7	15:63672634	GAGGCTGATGGGCTA[C/G]TAGTAACTGGTGTCT	8925
rs754467249	in-del	-/T/TTT/TTTT			intron-variant	HERC1	GRCh38.p7	15:63757262	CCAGTTTTTATTTAC[-/T/TTT/TTTT]TTTTTTTTTTTTTTT	8925
rs754502515	snp	A/C/G	3.34959e-05	0.00409232	intron-variant	HERC1	GRCh38.p7	15:63635913	GAAACCTATTCAACA[A/C/G]CTAGTATATTTACAA	8925
rs754506299	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63735270	CTTGCTTGAGCACAC[A/T]AACAGGGCAATTAAC	8925
rs754514208	snp	C/T	1.76518e-05	0.00297079	intron-variant	HERC1	GRCh38.p7	15:63752893	ATTTAAATACAAGTA[C/T]TACTTTTTAGTCACC	8925
rs754529098	snp	C/T	1.68898e-05	0.00290596	intron-variant	HERC1	GRCh38.p7	15:63716266	TCAAAAAGCATGCCA[C/T]AGTTTGTATCTAGAA	8925
rs754532470	snp	C/T	2.3111e-05	0.00339926	intron-variant, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609300	AGCCGTGACTGGGGA[C/T]ATCAGAGTGCCATAA	8925
rs754539328	snp	C/T	5.23693e-05	0.00511682	missense	HERC1	GRCh38.p7	15:63626091	TGAATGCTGACTTCT[C/T]TCAGCGCCCCATACT	8925
rs754540726	snp	C/T	1.68707e-05	0.00290432	intron-variant	HERC1	GRCh38.p7	15:63680798	TAAAAGTGGGATATT[C/T]ATTAATACTCAAAAA	8925
rs754542602	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63700990	TTAACTTACAAATGA[C/T]AGATTCTGGCTCCTC	8925
rs754552661	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63670154	GAAAGTAATGGTTTA[C/T]AGGCAAGTTATGGAA	8925
rs754552782	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63800756	GTAATTTCCTTTGTG[A/G]TAGGGGAATAGGAGC	8925
rs754554290	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63715313	CCAGATGACTATCAT[G/T]CTTTTATTGTAATTG	8925
rs754563295	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63792721	GAGATTTTCTCCACA[C/T]GCCAAGCAAGCAATC	8925
rs754570718	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63712675	TTTGAAAAAATTTTT[-/A]TATGTCTAAAACAAA	8925
rs754577074	snp	C/G	1.6908e-05	0.00290753	intron-variant	HERC1	GRCh38.p7	15:63694562	CTTCTAAAAGACAAA[C/G]AGACAGTTAAGAATC	8925
rs754578199	snp	C/T	4.96956e-05	0.00498451	missense	HERC1	GRCh38.p7	15:63674912	TCTGCTCAACATCCC[C/T]TTTCTCCTCGGATTC	8925
rs754581653	snp	A/G	1.67427e-05	0.00289328	intron-variant	HERC1	GRCh38.p7	15:63663223	AGAACAAAACAAAAA[A/G]GGCATTTTATTTGCA	8925
rs754593141	snp	C/G	5.46503e-05	0.00522706	intron-variant	HERC1	GRCh38.p7	15:63656082	AAAGTACTGAAAGTA[C/G]CTTACCTGTGTACAC	8925
rs754595820	snp	A/G	3.3162e-05	0.00407184	synonymous-codon	HERC1	GRCh38.p7	15:63674844	ACTCTGACTTTTGAC[A/G]TCATCAGATGTTAGG	8925
rs754621020	in-del	-/AAAAAAAAAAAG			intron-variant	HERC1	GRCh38.p7	15:63687538	CGAGACTCTGTCTCA[-/AAAAAAAAAAAG]AAAAAAAAAAAGAAA	8925
rs754624986	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63733961	TGAGGCCAGGAGTTC[A/G]AGAACAGCCTGGGAA	8925
rs754630847	snp	C/T	1.65622e-05	0.00287764	synonymous-codon	HERC1	GRCh38.p7	15:63725467	TACCCAGGACTGAGC[C/T]GGCTGAGGTAATGGC	8925
rs754632241	snp	A/C	1.65636e-05	0.00287776	missense	HERC1	GRCh38.p7	15:63686443	AGTTAAAATCTGTCC[A/C]TTCTCCACTAGGCAA	8925
rs754632485	snp	C/T	1.72764e-05	0.00293903	intron-variant	HERC1	GRCh38.p7	15:63658529	TAGCATCATGTGACA[C/T]AAAATAACACTTACC	8925
rs754640982	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63823645	ATGGTACATAACTAG[C/T]GCCATCCTACATTGG	8925
rs754654080	snp	A/G	3.45692e-05	0.00415733	intron-variant	HERC1	GRCh38.p7	15:63656375	TGCCAGTAAAGAAAA[A/G]CATCTCAGATGGATA	8925
rs754654828	snp	C/T	1.66263e-05	0.00288321	intron-variant	HERC1	GRCh38.p7	15:63764051	ATACATGCCATAGCA[C/T]TTTAACACAAAGTTG	8925
rs754663051	snp	C/T	3.94003e-05	0.00443831	missense	HERC1	GRCh38.p7	15:63655922	AGTCATCAACTGTGG[C/T]TAGATTTACACCTGT	8925
rs754680043	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63747212	TGCCTGTAATCCCAG[A/C]ACTTTGGGAGGCGGA	8925
rs754689164	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63714017	GAAATGCAAATTATC[A/G]GGCCCACCCCAGACC	8925
rs754692540	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63625384	TAGAAATGGCTGGTA[C/G]AAGTGGCTGGCAGAC	8925
rs754692866	in-del	-/TTC			intron-variant	HERC1	GRCh38.p7	15:63738929	CTCACCACCAGGATA[-/TTC]CTCCAACCCCATTTG	8925
rs754701907	snp	C/G	1.65671e-05	0.00287807	missense	HERC1	GRCh38.p7	15:63638733	CTGGAAGTTGCCCAA[C/G]ACATAATTTGTTCAT	8925
rs754714363	in-del	-/ACA	1.97896e-05	0.00314554	intron-variant	HERC1	GRCh38.p7	15:63716495	AAATTATCAGAAACT[-/ACA]ACACTAAATACATTT	8925
rs754716293	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63644018	AGCTTTAGAAGTGAC[-/A]ATAGGTAAGGCCTGT	8925
rs754717463	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63668631	TAAAAAGCAGGAGTG[A/G]CTATAACATCAGAGA	8925
rs754722179	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63816318	TCCAGAGCCCTTTTG[C/T]CAAGGAGCCACATTG	8925
rs754728413	snp	C/G	8.46991e-05	0.0065071	intron-variant	HERC1	GRCh38.p7	15:63723162	CTACAAATTTACTCC[C/G]TTTATCTTCTTTATC	8925
rs754733271	snp	A/T	0.000299267	0.0122288	synonymous-codon	HERC1	GRCh38.p7	15:63634808	ATTTCCAAGACCCAG[A/T]CGACCATAGTCACCA	8925
rs754742610	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63712727	AGCCTTACATATCAT[A/G]TACCTTGAAAACAAA	8925
rs754743168	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63666286	TCATAGCCTCTTAAA[A/G]GTTATGTTGTCTTTA	8925
rs754753359	snp	A/T	3.40408e-05	0.00412544	intron-variant	HERC1	GRCh38.p7	15:63630640	TATCAGGCGATCTGA[A/T]AAAAACAAAACAAAA	8925
rs754753464	snp	A/T	1.65605e-05	0.0028775	missense	HERC1	GRCh38.p7	15:63661834	AACAGGTAGTACGGA[A/T]TTCCACTCCCACATT	8925
rs754763662	snp	C/T	3.31702e-05	0.00407235	missense	HERC1	GRCh38.p7	15:63775289	AGTGCATAAAAGACA[C/T]GCTGGAGTACAAGCA	8925
rs754764703	snp	C/T	1.66241e-05	0.00288302	missense	HERC1	GRCh38.p7	15:63732965	GGGTCTTCATCAAAA[C/T]TTCAGCCAGGTGGGT	8925
rs754768655	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63650369	ACAGAGCAAGACTCC[A/G]TCTCAAAATAAATAA	8925
rs754780460	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63623973	TTCCCATCAGTGAAT[A/G]AAAAAGCTAGTTTAA	8925
rs754803229	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63681008	TGAATATCTATAGTA[C/T]TTAAAATAAGCAATT	8925
rs754806172	snp	A/C			missense	HERC1	GRCh38.p7	15:63674901	ACTCTCAGGTTTCTG[A/C]TCAACATCCCCTTTC	8925
rs754808106	in-del	-/ATATATAT			intron-variant	HERC1	GRCh38.p7	15:63737517	ATATCTTTTTTCCAG[-/ATATATAT]ATATATATATATATA	8925
rs754817441	snp	A/C	7.47775e-05	0.00611418	missense	HERC1	GRCh38.p7	15:63723259	CCCAATGCCAAGTCT[A/C]CATAGACAGCAATTT	8925
rs754830883	snp	C/G	2.14793e-05	0.00327707	intron-variant	HERC1	GRCh38.p7	15:63698706	CCAGAGCTCTCATAA[C/G]GAGTAAATATCAAAG	8925
rs754833221	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63801992	TAAAACTGAACTCTC[A/G]ACGTCTACCAACCCA	8925
rs754839829	in-del	-/AAACC	8.84917e-05	0.00665117	intron-variant	HERC1	GRCh38.p7	15:63689578	AATACCTTTTAGGAA[-/AAACC]AATTACCTGTAGTTT	8925
rs754846241	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63773269	GTCAACATGGTGAAA[A/C]CCCGTCTCTACTAAA	8925
rs754849846	snp	C/T	1.68142e-05	0.00289945	missense	HERC1	GRCh38.p7	15:63756601	ATGAAACCTTTTTAA[C/T]GGATCTGTGAGGCTC	8925
rs754867002	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63726127	GCTGGGAGTATAGGT[A/G]TGCACCACGGTGCCT	8925
rs754871487	snp	A/G			synonymous-codon	HERC1	GRCh38.p7	15:63649735	TTTACCATCCTTTCG[A/G]TAGCAATGCTCCAAT	8925
rs754876718	snp	G/T	0.000124701	0.00789526	intron-variant	HERC1	GRCh38.p7	15:63615945	GAAGAAAACAGAATT[G/T]TTATTACATGGTAGA	8925
rs754891975	snp	C/T	5.03326e-05	0.00501635	intron-variant	HERC1	GRCh38.p7	15:63666501	AAGAGAAATAAGAAC[C/T]TAAATATCACTAGAT	8925
rs754896509	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63771827	AGGAACCTCCCTGAC[C/T]AGCGAATTTGCTATT	8925
rs754901303	snp	C/T	1.76683e-05	0.00297218	intron-variant	HERC1	GRCh38.p7	15:63692383	TAATATCTATAAATA[C/T]TCTAAGACAAAGGCA	8925
rs754903267	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63741587	GCTGGGATTACAGGC[A/G]TGCGCCTGGCCCTAT	8925
rs754932554	snp	C/T	1.65688e-05	0.00287821	missense	HERC1	GRCh38.p7	15:63666380	CCATGGCTTTGGCAA[C/T]CTGCCGAAGAGAGAA	8925
rs754932962	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63826662	CTACATGTATGAATG[C/T]AGTATTAGTGGACAA	8925
rs754946723	in-del	-/G			intron-variant	HERC1	GRCh38.p7	15:63811670	CAAAATTAGCCGGGT[-/G]TGGTGGCAGGTGCCT	8925
rs754955015	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63812892	ATTATAAAATGTCAA[C/T]TGTCCCCCAAATTGA	8925
rs754960779	snp	C/T	0.000172058	0.00927358	intron-variant	HERC1	GRCh38.p7	15:63649965	GTTTTTACTTAATTC[C/T]TAAAAAGAAAAAAAG	8925
rs754961931	snp	C/T	5.0531e-05	0.00502623	synonymous-codon	HERC1	GRCh38.p7	15:63729632	ACTATTCTTTTCTAG[C/T]TCTCCAAATGCTTGA	8925
rs754969414	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63780443	GGTAAAACAGAAGGC[C/T]GGGCGCGGTGGCTCA	8925
rs754969605	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63661082	GTTAGTACCCCAAGA[C/T]GCAAATTAAGTCATT	8925
rs754970401	snp	C/T	6.62405e-05	0.00575464	missense	HERC1	GRCh38.p7	15:63645036	CTTCTGCACTAGTCA[C/T]ATTGGTCTGTGTAGT	8925
rs754970683	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63833036	ATAACATGTCTTTTA[C/T]ATAACCTCCTGGGAG	8925
rs754979029	in-del	-/C			intron-variant	HERC1	GRCh38.p7	15:63683637	TATTGTCAGGTCCTA[-/C]CACCATCTAAGGTTT	8925
rs754984685	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63797240	CTAAGGTGTAGGCAT[A/G]GTTTCTATCATCCCT	8925
rs754988327	snp	A/C			upstream-variant-2KB	HERC1	GRCh38.p7	15:63835603	GTGCAATGGCACCAT[A/C]TTGGCTCACTGCAAC	8925
rs754990852	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63661338	GGCAACAAACCTACT[C/T]TCTAGGGATTAAGGA	8925
rs754997594	snp	A/G	1.65765e-05	0.00287888	stop-gained	HERC1	GRCh38.p7	15:63713399	TTGTTGAAGGTTGCT[A/G]CAACTGTCCTTCTTC	8925
rs755002094	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63690908	AGATACTATGCTATG[C/T]TACACATTTCACACA	8925
rs755004766	snp	C/G/T	3.3188e-05	0.00407346	intron-variant	HERC1	GRCh38.p7	15:63638552	CTAGAAAACCACAAT[C/G/T]ATCTCAAAATTAGAG	8925
rs755013442	snp	G/T	1.67343e-05	0.00289255	missense	HERC1	GRCh38.p7	15:63641606	AAAACATGATTGGCA[G/T]CTGCCCATTCTGCTG	8925
rs755019875	snp	A/G	8.28919e-05	0.00643732	synonymous-codon	HERC1	GRCh38.p7	15:63727801	GGAGTTAACAATCTG[A/G]CAGAGCATACTGCCA	8925
rs755030172	snp	A/G	5.45123e-05	0.00522046	synonymous-codon	HERC1	GRCh38.p7	15:63642972	CTTTGATCTATTTGA[A/G]CAAGCAGCTACTCCA	8925
rs755068375	snp	A/G	3.31285e-05	0.00406978	synonymous-codon	HERC1	GRCh38.p7	15:63636093	TTCAGTTAGGGCCAT[A/G]GAGTGCCCATCAGAA	8925
rs755085944	snp	A/C	1.74766e-05	0.00295601	intron-variant	HERC1	GRCh38.p7	15:63624118	ACATCCATCTGAAAA[A/C]ATCACAGCTCATTAG	8925
rs755091753	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63706407	AACACCATTTAAACT[A/G]TAACAACTCTGTGAG	8925
rs755094204	snp	A/G	1.65765e-05	0.00287888	intron-variant	HERC1	GRCh38.p7	15:63694726	AGTACCATAACCTCG[A/G]GCTAAAATGTAACCT	8925
rs755109337	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63796172	GAAGAGGAACCTTTA[G/T]TTTTTACAAGTAGAA	8925
rs755140977	snp	C/T	1.65611e-05	0.00287755	synonymous-codon	HERC1	GRCh38.p7	15:63612491	CTGCTCCAGTTGTTT[C/T]GCTGTGAGGAGGGAC	8925
rs755144963	snp	C/G	1.72958e-05	0.00294068	intron-variant	HERC1	GRCh38.p7	15:63686584	ATAATCCATGTCTCA[C/G]ATAAGATATATTCTG	8925
rs755147167	snp	C/T	0.000315937	0.0125646	synonymous-codon	HERC1	GRCh38.p7	15:63694841	TTGATAAATTTTATG[C/T]ACAGCTACCTGGATT	8925
rs755159524	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63766189	CTATTAATATAATCA[C/T]AGAGGTCAAACATTA	8925
rs755170538	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63673409	AGCTAAGACAAGAAG[A/C]AAAGGAATAAGTACA	8925
rs755172862	snp	A/G	3.93771e-05	0.004437	intron-variant	HERC1	GRCh38.p7	15:63678388	AAAGTAAAGAGGGTG[A/G]AAAACACATGCTATT	8925
rs755176046	in-del	-/ATAA	1.68158e-05	0.00289959	intron-variant	HERC1	GRCh38.p7	15:63754485	AAGCCAAAGCTACTG[-/ATAA]ATAATTTTTTACATA	8925
rs755176790	in-del	-/G			intron-variant	HERC1	GRCh38.p7	15:63745418	GTGGCAAGCCTTGCA[-/G]GAATTCAAATTTGGA	8925
rs755176851	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63774685	AAAGTTGAGACTTAT[A/C]GTACGTACCAAAGAA	8925
rs755185919	snp	A/G	3.3305e-05	0.00408061	missense	HERC1	GRCh38.p7	15:63623855	TTAACTACTTGTCTC[A/G]CTATTTGGACAAAAA	8925
rs755204843	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63686052	GACAAAAACATCACA[C/T]GCTTTGCTTCATTTT	8925
rs755210169	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63717495	ACGATCATGTTATCA[A/T]GATTACCAAGCACTT	8925
rs755228005	snp	A/G	1.71519e-05	0.00292842	stop-gained	HERC1	GRCh38.p7	15:63674510	ACTGCAGGGCTGCTC[A/G]CATCTCCACGTCTTC	8925
rs755234884	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63643333	TTTCTACAATTGGTT[A/C]ATTTTTATCACATGT	8925
rs755259116	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63805146	TTTATAGCGTCTTTA[C/T]TCATAATAGCCAAAA	8925
rs755266133	snp	C/G/T	3.68692e-05	0.00429343	synonymous-codon, missense	HERC1	GRCh38.p7	15:63649837	CAACAATTCTGGAGA[C/G/T]TCTCCTGACCAGGCT	8925
rs755267856	in-del	-/A	0.474482	0.137369	intron-variant	HERC1	GRCh38.p7	15:63674314	CAACAGCACAAAAGC[-/A]AAAAAAAAAAAAAAT	8925
rs755274582	snp	C/G	4.47417e-05	0.00472957	missense	HERC1	GRCh38.p7	15:63747061	GTAGCTTCAGGCACA[C/G]CTTGAGAAAACTGTG	8925
rs755282997	in-del	-/G			intron-variant	HERC1	GRCh38.p7	15:63822849	AAATAGAGCCAAGAT[-/G]ATTTGCTAATAGACT	8925
rs755286055	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63764977	CAGTGGCAAAGATTA[C/T]TGCTGTGAAAAGGAA	8925
rs755292109	snp	A/G	4.78847e-05	0.00489286	intron-variant	HERC1	GRCh38.p7	15:63756773	AAGAATCATAAATAT[A/G]AAATACTTCTGTGAG	8925
rs755292840	snp	C/T	0.00040828	0.0142819	missense	HERC1	GRCh38.p7	15:63632727	GACCAAAGGTATACA[C/T]ATGACCATCTTTGGT	8925
rs755322988	snp	C/T			intron-variant, missense	HERC1	GRCh38.p7	15:63654375	AATTGGGCAATTAAA[C/T]CTGCTTAAACAAAAC	8925
rs755327930	snp	A/G	1.65696e-05	0.00287828	synonymous-codon	HERC1	GRCh38.p7	15:63698917	CTCAAAGGAATAGGA[A/G]GAGTTGCATAACCAG	8925
rs755330650	snp	C/G	2.52892e-05	0.00355584	intron-variant	HERC1	GRCh38.p7	15:63755197	ATTTCTAATTTTCTA[C/G]AAGAATAACTTACAT	8925
rs755331278	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63642308	AATGTCTTTGCAATG[C/T]TTCTCCTTTTCAAGG	8925
rs755353533	snp	A/G	1.88973e-05	0.00307381	missense	HERC1	GRCh38.p7	15:63645483	AAATTGACAACATAC[A/G]TAGCCATCAGTAACT	8925
rs755354320	snp	C/G	1.6582e-05	0.00287936	missense	HERC1	GRCh38.p7	15:63754553	TCCCATCTTTAGACA[C/G]AGCAATAGTATGTGA	8925
rs755356608	snp	C/T	1.68289e-05	0.00290072	intron-variant	HERC1	GRCh38.p7	15:63628838	TAAATCACAAATATA[C/T]AGACATTCAATTAGA	8925
rs755359353	snp	A/G	4.96899e-05	0.00498422	missense	HERC1	GRCh38.p7	15:63677917	ACCACTCCCAGCAGC[A/G]TGGCATGGCGCCCAG	8925
rs755361905	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63676179	ACTGCCGGGATTACA[A/T]GTGTGAGCCACCAAG	8925
rs755365504	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63788573	AGTACAGCTGTAATA[C/G]TACCACAGTTGTGGA	8925
rs755381283	snp	A/G	8.4386e-05	0.00649507	missense	HERC1	GRCh38.p7	15:63698990	TCCAATTGACTGTGC[A/G]TAGGACCTATATACA	8925
rs755383386	in-del	-/AC	1.66717e-05	0.00288714	intron-variant	HERC1	GRCh38.p7	15:63654093	TACATAACGTGATTA[-/AC]ACACTTTCCACTCAA	8925
rs755396362	snp	C/G	1.65616e-05	0.00287759	synonymous-codon	HERC1	GRCh38.p7	15:63733101	TAGGGAGGCTACGTG[C/G]GTATGATCTTGCAAA	8925
rs755401231	snp	C/T	1.66713e-05	0.0028871	synonymous-codon	HERC1	GRCh38.p7	15:63616595	GTCCAGAGGCTTCTT[C/T]GTGCGAATGGCAACC	8925
rs755401847	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63622070	TTTAATTTACAAGTC[C/T]ATGAAACAGGATCCA	8925
rs755410658	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63830278	ACCATGTACCCCCAA[A/T]ATGATGCATTGAGAA	8925
rs755425698	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63701397	ATTCTATGGAATGGC[C/T]GACGAAGCCCAAAAT	8925
rs755432380	snp	A/C/G	4.15285e-05	0.00455662	intron-variant	HERC1	GRCh38.p7	15:63716505	GAAACTACACTAAAT[A/C/G]CATTTTTTCCAAAAT	8925
rs755434201	in-del	-/A	1.66034e-05	0.00288122	frameshift-variant	HERC1	GRCh38.p7	15:63638427	TGTTGGGCCTGTGAG[-/A]ATGAGGGAGCTGCTG	8925
rs755466760	snp	A/C	2.32637e-05	0.00341047	intron-variant	HERC1	GRCh38.p7	15:63729211	TTAATGACTGATTAA[A/C]TTTGAAATGAAATAC	8925
rs755487418	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63616307	GGGCAGCAATGGCAT[A/T]GATATGGCATTGTTC	8925
rs755490831	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63787479	TATTTAAATTAAAAA[A/T]ATATATCTGGCAGAT	8925
rs755492286	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63664336	GCATAGAAAATGATA[C/T]CCAAATAGCTGTTCT	8925
rs755508673	snp	C/G	1.79583e-05	0.00299647	intron-variant	HERC1	GRCh38.p7	15:63675154	CACAGGAAGAAGCAA[C/G]TGAGGGAAAGACGGG	8925
rs755548427	snp	A/G	0.000186272	0.0096489	intron-variant	HERC1	GRCh38.p7	15:63637105	TCTCTCCAAGTCACA[A/G]AGAACTCTGATGAAG	8925
rs755552704	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63811227	TCGGTGTGATAAAAG[C/T]ATTGTGGTTAAGTTG	8925
rs755553525	snp	A/G	6.65823e-05	0.00576947	missense	HERC1	GRCh38.p7	15:63659841	GTTCTGGTACAATGC[A/G]CCGGTCATTTAAACC	8925
rs755553890	snp	A/G	1.68502e-05	0.00290255	intron-variant	HERC1	GRCh38.p7	15:63615964	TTACATGGTAGAAAT[A/G]ACAGCAAAAAGTATT	8925
rs755568838	snp	C/T	3.31214e-05	0.00406935	missense	HERC1	GRCh38.p7	15:63645051	CATTGGTCTGTGTAG[C/T]ATCTTGAGGAATGCG	8925
rs755570734	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63811489	TAGAAACAGCTGAAT[C/G]AGGCACAGCTGAGCC	8925
rs755580338	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63676689	TGAACCCGGGAGGCA[A/G]AAGTTGCAGTGAGCC	8925
rs755590028	snp	C/G	3.31279e-05	0.00406975	missense	HERC1	GRCh38.p7	15:63654171	TTTCTAAGATCTCCT[C/G]CCATATCAGCAAGTG	8925
rs755591739	snp	C/T	1.68707e-05	0.00290432	intron-variant	HERC1	GRCh38.p7	15:63666512	GAACCTAAATATCAC[C/T]AGATACCGTGAGTAA	8925
rs755604433	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63724101	GTTTCATGATTTTAT[A/G]ACTTAAAAAGTGAAA	8925
rs755611955	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63799699	GAAGATGGAAAATGA[A/T]AGGACAATAAAATGC	8925
rs755614105	snp	A/G	1.65658e-05	0.00287795	synonymous-codon	HERC1	GRCh38.p7	15:63654143	ATGAGCCTCCAATTT[A/G]ATAAAGGAGCATTTT	8925
rs755623858	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63689459	ATCAGTGGAAAGGGA[A/G]ACAGAATGCCAAGAG	8925
rs755626350	snp	A/T	3.575e-05	0.00422773	intron-variant	HERC1	GRCh38.p7	15:63716476	GGTTTTCTGATATCT[A/T]AAAGAAATTATCAGA	8925
rs755634840	in-del	-/AAG	0.000585766	0.0171038	intron-variant	HERC1	GRCh38.p7	15:63655696	ACATTATTTAAAAAT[-/AAG]AAGTCGATTAGAAGA	8925
rs755653841	in-del	-/TG			intron-variant	HERC1	GRCh38.p7	15:63829544	GTGCACATATATGTA[-/TG]TGTGTGTGTGTGTGT	8925
rs755656959	snp	C/T	1.65756e-05	0.00287881	synonymous-codon	HERC1	GRCh38.p7	15:63732984	AGCCAGGTGGGTATC[C/T]GGATGGCAGCTCTGA	8925
rs755658022	snp	G/T	8.22132e-05	0.00641091	missense	HERC1	GRCh38.p7	15:63723218	GCATGCTGATCCAAA[G/T]GCTTCGGGCAGGCTC	8925
rs755660453	snp	G/T	1.75557e-05	0.00296269	intron-variant	HERC1	GRCh38.p7	15:63626178	AAAGCAAATGGGCAC[G/T]TATGAAGGAAACAGC	8925
rs755675949	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63736735	TGCCTCAGCCTTAAG[G/T]AGCTGGGATTACAGG	8925
rs755693890	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63782397	TGCTCTACTAATCCA[A/G]CAACGAAGCCTGGAT	8925
rs755713814	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63688284	GTGAGGCATCAAGAT[C/G]ACTCCTAGGTTTTTC	8925
rs755725767	snp	A/G	1.656e-05	0.00287745	intron-variant	HERC1	GRCh38.p7	15:63692590	AAGAGACAAGTTTAC[A/G]TTACAACCAAGAGCC	8925
rs755725831	snp	A/G	1.65666e-05	0.00287802	missense	HERC1	GRCh38.p7	15:63698858	CTTACAACATTTTCA[A/G]TCAAAGTGTGAACTC	8925
rs755727012	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63750063	GAGGGTCTGCTAAAC[C/T]ACTAATCGGCTTGCA	8925
rs755748752	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63822821	ATGTGATCAGATTAG[A/G]AATGTATTCAGAAAA	8925
rs755749475	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63781339	CTCATTTGAGCAAGT[A/G]TATTGGTGCCATTTT	8925
rs755751612	snp	A/G	1.65682e-05	0.00287817	missense	HERC1	GRCh38.p7	15:63666391	GCAATCTGCCGAAGA[A/G]AGAACCCCATTTCCA	8925
rs755759806	snp	C/T			upstream-variant-2KB	HERC1	GRCh38.p7	15:63834806	ACTCCTTTCCAGCCA[C/T]CTTCATGGTGTCTTT	8925
rs755764816	in-del	-/AC			intron-variant	HERC1	GRCh38.p7	15:63813314	TAATCAGAGATGGAC[-/AC]ACACACACACACACA	8925
rs755766177	snp	A/G	1.73222e-05	0.00294292	intron-variant	HERC1	GRCh38.p7	15:63752902	CAAGTATTACTTTTT[A/G]GTCACCTAATCCTCT	8925
rs755790170	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63646878	ACTATCTGGTAAAGA[C/T]GCTTTTACCAGAATA	8925
rs755805821	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63821184	CCCAGCACTTTGGGA[A/G]GCTGGGGTGAGAGGA	8925
rs755829541	snp	C/T	0.000233581	0.0108044	missense	HERC1	GRCh38.p7	15:63632802	CAATTCCACAAAGGA[C/T]GTCAATTTTCTACAA	8925
rs755853841	snp	C/G	1.98671e-05	0.00315169	utr-variant-3-prime, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609072	GGGAGGGTGAGAGCA[C/G]CCGCACGGTCAGTAG	8925
rs755856112	snp	C/G	1.75779e-05	0.00296457	intron-variant	HERC1	GRCh38.p7	15:63713325	GGGAAGTGAGTAGGT[C/G]ATGTTTTCAGTGTCT	8925
rs755873428	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63631120	AGTAGCTTGGACCAC[A/C]GGCACATGCCACCAT	8925
rs755875210	snp	A/G/T	6.46466e-05	0.00568505	intron-variant	HERC1	GRCh38.p7	15:63774670	ACTATTATGAACTTT[A/G/T]AAGTTGAGACTTATA	8925
rs755877071	snp	A/C	1.72071e-05	0.00293313	stop-gained	HERC1	GRCh38.p7	15:63775584	AGCTGTTCAAGTGTT[A/C]AAGCCATTTCAGCTT	8925
rs755880560	snp	A/G	0.000156108	0.00883343	intron-variant	HERC1	GRCh38.p7	15:63624136	CACAGCTCATTAGTC[A/G]AACACACATACATAT	8925
rs755887878	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63701169	AGAGACCTTAAAGAT[C/T]ATTTAGTCCAATTTT	8925
rs755893599	snp	A/G	1.7342e-05	0.0029446	missense	HERC1	GRCh38.p7	15:63626097	CTGACTTCTCTCAGC[A/G]CCCCATACTGGGGGG	8925
rs755918217	snp	A/G	1.75718e-05	0.00296405	intron-variant	HERC1	GRCh38.p7	15:63756793	ACTTCTGTGAGTATC[A/G]AAGTATAATATTTAA	8925
rs755918293	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63671479	TTATTCCAGTAAGAG[A/G]GCTAACATGTAGGAG	8925
rs755921970	snp	C/T	1.73754e-05	0.00294744	missense	HERC1	GRCh38.p7	15:63674534	CGTCTTCATGAACAA[C/T]TGGAGAACTTGCACA	8925
rs755933461	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63748882	TGATGGACTAAACAC[A/G]TACAGTTAGCACTTT	8925
rs755953420	snp	C/T	0.00033129	0.0128661	synonymous-codon	HERC1	GRCh38.p7	15:63713421	TCCTTCTTCTCTTCG[C/T]TTCTGAAGCTCATCT	8925
rs755954554	snp	A/G	6.62427e-05	0.00575473	synonymous-codon	HERC1	GRCh38.p7	15:63733044	GTAGCCAGTACACAC[A/G]GAAGATAGGTCAGCA	8925
rs755958301	snp	A/C/G/T	6.70777e-05	0.00579097	intron-variant	HERC1	GRCh38.p7	15:63633991	GAAATAACAGCATTC[A/C/G/T]GTAAGGCAAATCACA	8925
rs755962355	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63833108	CTGCCACCCATCACA[A/G]AACAGATTTCACCAT	8925
rs755974407	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63640040	TTCCATTTCTCTTAA[A/G]GGTATCCTTCTAGCC	8925
rs755986838	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63762095	TTCAGAAAACTAGCT[A/G]GATGATTCCAGATTG	8925
rs755995012	snp	C/T	1.81017e-05	0.00300841	intron-variant	HERC1	GRCh38.p7	15:63680514	ACAAGAAAAATGTAA[C/T]GCTTGTGAATGGGTG	8925
rs755998321	in-del	-/G	1.68004e-05	0.00289826	intron-variant	HERC1	GRCh38.p7	15:63718760	AGCAAATATTTGTCT[-/G]AGGATAGTTTTAAGT	8925
rs755998336	snp	C/G	3.76939e-05	0.00434114	missense	HERC1	GRCh38.p7	15:63723269	AGTCTACATAGACAG[C/G]AATTTCAGGCCGCAA	8925
rs756001876	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63670389	CCACACTGACTGCTC[G/T]TCAGATTTGTCCAAA	8925
rs756006394	snp	A/G	1.65688e-05	0.00287821	missense	HERC1	GRCh38.p7	15:63758218	AGTTTGGGTTGCAGT[A/G]TTTTCTCCTGTGTAC	8925
rs756008269	snp	C/G	9.47015e-05	0.00688053	missense	HERC1	GRCh38.p7	15:63747782	TATCACAGTATCTCT[C/G]AAGAAAAGAACGCAG	8925
rs756011531	snp	A/G	3.41618e-05	0.00413276	intron-variant	HERC1	GRCh38.p7	15:63680034	CTGATGCTAAACAAT[A/G]AAATAACAAATATTC	8925
rs756015339	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63687063	AGAAATCAAATCATG[A/G]AAAACCTTGTGTGTC	8925
rs756022131	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63727546	GAAATTCCTTTGATA[G/T]CCTTAGGATAGATAG	8925
rs756029989	snp	A/C	1.65636e-05	0.00287776	synonymous-codon	HERC1	GRCh38.p7	15:63661974	GACGCTGCATTCACA[A/C]AGTTCACACACCACC	8925
rs756032829	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63792867	CTTCTGATTCCAATC[G/T]CAAGCCCCAGGTTGT	8925
rs756033843	snp	A/G	1.70142e-05	0.00291664	missense	HERC1	GRCh38.p7	15:63678260	GAAGGATACGGATGA[A/G]CTGAATAGTGGCCTC	8925
rs756040005	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63644169	TCTCCCCATCCTTAA[A/G]CTCCTTCTTCCTTTT	8925
rs756042960	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63707576	ACATTATGGTATCAG[A/C]AATTTCAATTGTACT	8925
rs756054356	snp	C/T	0.000182632	0.00955419	synonymous-codon	HERC1	GRCh38.p7	15:63775309	GAGTACAAGCAGTCG[C/T]TTTCTAAGTGCCCCG	8925
rs756061525	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63731603	TAAATCTGAAAGAAA[A/C]GAATTTTGTAGGAAG	8925
rs756072759	snp	C/G	1.65589e-05	0.00287736	missense	HERC1	GRCh38.p7	15:63661861	CATTCACCGCCAAAC[C/G]AGCCATCCACATAGG	8925
rs756073146	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63693539	GTGAGCCACTGCGCC[C/T]GGCCTGGGGGACAAT	8925
rs756077703	snp	C/T	2.08792e-05	0.00323097	intron-variant	HERC1	GRCh38.p7	15:63774674	TTATGAACTTTAAAG[C/T]TGAGACTTATAGTAC	8925
rs756098685	snp	A/T	3.33773e-05	0.00408504	intron-variant	HERC1	GRCh38.p7	15:63640146	AGCAGCTCACAGTAC[A/T]TTTACCATTAGAAAT	8925
rs756104240	snp	C/G	1.98301e-05	0.00314875	intron-variant	HERC1	GRCh38.p7	15:63643397	AAAATAAAATCTATG[C/G]TCTTACCCTTAAAGA	8925
rs756108105	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63814183	AAAAATCTGGACAAC[C/T]ATACATCATAATTTA	8925
rs756116771	snp	C/T	1.6604e-05	0.00288127	missense	HERC1	GRCh38.p7	15:63675037	GTCAGGCCTCGGAAT[C/T]GCGCCACATCAAACG	8925
rs756121133	snp	A/G	1.6566e-05	0.00287797	stop-gained	HERC1	GRCh38.p7	15:63774852	ATCGCAATGAGCCTC[A/G]TTGAGCTGCCAAACC	8925
rs756130735	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63641035	CAATTCAACATAGCT[C/T]TTCCACTAAATTTTC	8925
rs756145293	snp	A/G	8.54975e-05	0.00653769	intron-variant	HERC1	GRCh38.p7	15:63729229	TGAAATGAAATACCA[A/G]ACTCACCTCTTAATT	8925
rs756157399	snp	C/T	1.68596e-05	0.00290336	intron-variant	HERC1	GRCh38.p7	15:63638378	AATTTTCAGTTCCCA[C/T]GTTTCTTTTCTATTT	8925
rs756166723	snp	G/T	1.8182e-05	0.00301507	missense	HERC1	GRCh38.p7	15:63656092	AAGTAGCTTACCTGT[G/T]TACACAACTGTACAA	8925
rs756171697	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63709076	CTCACTATAACCTCC[A/G]CCTCCCAGATTCAAG	8925
rs756184478	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63610147	AAAAAAAAAAAAAAG[-/A]AACCTGTCTTCTCTC	8925
rs756198665	snp	C/T	1.65726e-05	0.00287855	synonymous-codon	HERC1	GRCh38.p7	15:63628756	CTGCCGAACATTTTT[C/T]CCTTGCAGACCTGTT	8925
rs756204757	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63650208	AGGAATTCGAGACCA[A/G]CCTAGTCAACATGGT	8925
rs756210841	snp	C/T	3.3129e-05	0.00406982	synonymous-codon	HERC1	GRCh38.p7	15:63775009	ATTTGCTAATGATAA[C/T]GGTGGCAAAGAGCTC	8925
rs756211434	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63787297	GAGTAGGTGGGACTA[A/C]AGGCATGCACCACCA	8925
rs756213043	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63663341	GACCATAAAACATCA[A/T]ATTATACCTATCACG	8925
rs756215238	in-del	-/AAC			intron-variant	HERC1	GRCh38.p7	15:63700444	CAGAGAAAACAAACT[-/AAC]AACAATATTCAATGT	8925
rs756218712	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63798312	CCAAATGACTACTCA[G/T]TGCTTAACCAGTTAA	8925
rs756218742	snp	A/G	3.37098e-05	0.00410533	synonymous-codon	HERC1	GRCh38.p7	15:63690544	AAAAATAAAAACCTG[A/G]GCCATTTGATCATCT	8925
rs756230250	snp	A/G	1.6701e-05	0.00288968	synonymous-codon	HERC1	GRCh38.p7	15:63692505	TGAAGATACAACTCT[A/G]CGAAGAAAAACTAAA	8925
rs756246264	snp	A/G	1.77957e-05	0.00298287	intron-variant	HERC1	GRCh38.p7	15:63612586	GGTTGCTCATTCAAT[A/G]AGTGTGCGTGAACCT	8925
rs756250611	in-del	-/G	1.73456e-05	0.00294491	frameshift-variant	HERC1	GRCh38.p7	15:63612303	TCAGCAGTGTTGGCT[-/G]GTAGTCGAGATCTTC	8925
rs756256258	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63784694	CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG	8925
rs756258554	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63741763	TCATGAAATAGTTTT[C/G]GCACTCTTGTAGAAA	8925
rs756258858	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63745322	ACCAGTTCAGCACTA[C/G]GACTCGCCTAAGAGT	8925
rs756289514	snp	C/G	1.65806e-05	0.00287924	missense	HERC1	GRCh38.p7	15:63624265	GACTCTTGGGGCTAA[C/G]AAAGGCCGAAGTTGT	8925
rs756296858	snp	C/T	1.68935e-05	0.00290628	intron-variant	HERC1	GRCh38.p7	15:63665913	GTACAGAAACTGGAA[C/T]TTCACCTTTCACTAA	8925
rs756304474	snp	A/G	2.46679e-05	0.00351189	intron-variant	HERC1	GRCh38.p7	15:63696112	CTGTATATACTGCAA[A/G]GTGTCACCTACCTGA	8925
rs756311920	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63754977	GATCATGATGGTATT[C/G]CTTTTATCCCAGAAA	8925
rs756322318	snp	C/T	1.72928e-05	0.00294043	missense	HERC1	GRCh38.p7	15:63694870	TTTCAATCTGAATAT[C/T]TCTCTTAGCTGCTCT	8925
rs756326638	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63811538	AAAGGGGCCGGGCGC[A/G]GTGGCTCACGCCTGT	8925
rs756330502	snp	A/G	1.67153e-05	0.00289091	synonymous-codon	HERC1	GRCh38.p7	15:63674697	TTCTGACTGGGCTAC[A/G]TCATGGTTTTTGGAC	8925
rs756332339	snp	A/G	1.76505e-05	0.00297068	intron-variant	HERC1	GRCh38.p7	15:63677805	GCCTATTTCACCATT[A/G]AATATTTGTTTGCTA	8925
rs756332532	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63675480	ATAGTGCAAAAGCAG[A/C]CACTGATACAACTAA	8925
rs756340819	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63797397	AGAAAATCATTATAA[C/T]AGAATCTAAGATTGG	8925
rs756350795	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63659579	CCACATTATACCTTC[A/C]AAATGTTAAAACAAC	8925
rs756351606	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63674320	GCACAAAAGCAAAAA[A/G]AAAAAAAATCAGATA	8925
rs756351843	snp	C/T	8.28494e-05	0.00643567	missense	HERC1	GRCh38.p7	15:63666007	GATCATTTGACTTCC[C/T]GCCACTGCCTAGAAC	8925
rs756352951	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63825739	AACATCAGTTCATTA[G/T]AAAACCACGAAAAAA	8925
rs756374258	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63766550	CACCACTGCACTCCA[C/G]CCTAGGTGACAGAAT	8925
rs756375706	snp	A/T	5.69071e-05	0.00533388	synonymous-codon	HERC1	GRCh38.p7	15:63689697	AAATAAGCGCTCAAC[A/T]ATCTGTTTTATTGAA	8925
rs756389938	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63767526	CCATGCTGAAACCCC[A/C]TCTCTACTAAAAATA	8925
rs756391097	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63684853	CTCTACTAAAAATAT[-/A]AAAAAATTAGCCAGG	8925
rs756393916	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63778074	GAAGGAAAAATTAAA[G/T]TCTATACCAAACCAC	8925
rs756404290	snp	G/T	1.81972e-05	0.00301633	missense	HERC1	GRCh38.p7	15:63643016	ATACTGTGGTCTGAA[G/T]AGCTCCAGAGCCTAT	8925
rs756408399	snp	A/G	1.66172e-05	0.00288242	intron-variant	HERC1	GRCh38.p7	15:63727846	TATCACATCTATGAA[A/G]GGCAAGAAATTAAAC	8925
rs756416322	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63833346	CACCCCGCTAAAGGC[A/G]GCCGGCGCCTGGGGA	8925
rs756424940	snp	C/T	1.72083e-05	0.00293323	intron-variant	HERC1	GRCh38.p7	15:63755346	TTGCACACAAGTAAA[C/T]ACGATGAGTATGCAC	8925
rs756429644	in-del	-/TAAG			intron-variant	HERC1	GRCh38.p7	15:63825508	AATTTATACAATAAA[-/TAAG]TAAGTAAGCCTGAAA	8925
rs756443576	snp	A/C	2.02493e-05	0.00318186	missense	HERC1	GRCh38.p7	15:63734849	AAGTTTCAATTACCA[A/C]CTAATATCAAAAGAG	8925
rs756443988	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63733578	CATCTGTAGGCTGGG[C/T]GCAGTGGCTCACACC	8925
rs756458324	snp	C/G	9.96959e-05	0.00705961	intron-variant	HERC1	GRCh38.p7	15:63706876	ATTTAGTTGTGAAAA[C/G]TATTTTAAGATTAAG	8925
rs756465521	snp	C/T	1.69568e-05	0.00291172	missense	HERC1	GRCh38.p7	15:63648092	CATCAATTAGAACAA[C/T]GCCTCCTTTCTCAAG	8925
rs756486448	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63655422	AAGAGAAAGGCAGTA[C/T]TGATAAGTAGTCCCT	8925
rs756487485	snp	A/G	1.96277e-05	0.00313264	missense	HERC1	GRCh38.p7	15:63672613	CTCATAAAGGAGGTC[A/G]TGCTTGAGGCTGATG	8925
rs756499224	snp	A/T	9.12909e-05	0.00675552	intron-variant	HERC1	GRCh38.p7	15:63622912	GAAGAAAGAAAAAAA[A/T]TTTTTGAGAAATGAC	8925
rs756503635	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63630386	AGATTATGAATTTCC[C/T]AGCTTATCTCTTTCC	8925
rs756505832	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63644882	TATTTCCCAATGGAT[C/T]TTGCCCTTTGGGATA	8925
rs756513435	snp	C/T	3.33222e-05	0.00408167	synonymous-codon	HERC1	GRCh38.p7	15:63694416	CTGCAGGGGCTGTCC[C/T]AGCATGGTGTCTGTA	8925
rs756526536	in-del	-/CA			intron-variant	HERC1	GRCh38.p7	15:63625126	AATCTCACGCATGCA[-/CA]CACACACACACGCAC	8925
rs756533314	snp	A/G			synonymous-codon	HERC1	GRCh38.p7	15:63747005	CCCGAGAATGCTGGT[A/G]GCTACCCCTCCCGCA	8925
rs756534965	snp	A/G	1.76375e-05	0.00296958	missense, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609211	AGCTGGCTGGAGTAC[A/G]GGGGCAGCCTCAGCT	8925
rs756539757	in-del	-/TATCCTAC	1.65957e-05	0.00288055	frameshift-variant	HERC1	GRCh38.p7	15:63666463	GTCTACTGCTTGGGT[-/TATCCTAC]CTGACAAGGCTGAGA	8925
rs756546393	snp	A/G	3.40611e-05	0.00412667	intron-variant	HERC1	GRCh38.p7	15:63699001	GTGCATAGGACCTAT[A/G]TACAAACAGAATAAA	8925
rs756547006	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63819648	TAAGAAATCAAAGCA[A/T]TAGGTAGTCTCTAAA	8925
rs756563975	snp	C/T	3.33228e-05	0.0040817	synonymous-codon	HERC1	GRCh38.p7	15:63654263	TGCCCATTGCCGATG[C/T]TGTGAGGACAGCCTG	8925
rs756564324	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63831346	TCCTGGGCTCAAGCC[A/G]TCCTCCCACCTCGGC	8925
rs756593560	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63643673	GGGGAGAGATAATTT[A/C]TCTCATAAAGGATAG	8925
rs756594102	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63685286	TTAATTATTCAGACT[A/G]AACTGGGAGCACAGA	8925
rs756599183	snp	A/G	8.10997e-05	0.00636736	intron-variant	HERC1	GRCh38.p7	15:63659967	ATAAATGTATAGTAT[A/G]TGAATTTAAATATTA	8925
rs756604573	snp	C/T	1.84756e-05	0.00303932	intron-variant	HERC1	GRCh38.p7	15:63718732	AAAGTTACCTAATTT[C/T]TGACATCATGAGAGC	8925
rs756615367	snp	A/C	2.07842e-05	0.00322361	missense	HERC1	GRCh38.p7	15:63645619	AGAGTTTCACACTGT[A/C]TTCTTTGGCACATGT	8925
rs756637551	in-del	-/ATTTT			intron-variant	HERC1	GRCh38.p7	15:63728129	CATTAATTTATCTTC[-/ATTTT]ATAATTTACTCAAGA	8925
rs756640153	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63790867	GTTTGTATGACCATA[C/T]TGTTTTCAATTGTAA	8925
rs756642084	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63654498	TTTCACTAAAATATG[C/T]ACACAAGAAATAAAG	8925
rs756646071	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63623556	AAAGCGTTTCAAAAG[C/G]TGTTGCTCTAATTTA	8925
rs756675417	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63818747	GGACATACTAAACTT[C/T]TATCAACATTTCACT	8925
rs756682485	snp	A/G	4.2555e-05	0.00461256	intron-variant	HERC1	GRCh38.p7	15:63655704	TAAAAATAAGAAGTC[A/G]ATTAGAAGACTGTAT	8925
rs756684968	snp	C/T	0.000175166	0.00935694	intron-variant	HERC1	GRCh38.p7	15:63755210	TAGAAGAATAACTTA[C/T]ATTTTTAAAAAATCT	8925
rs756685277	snp	A/G	6.62745e-05	0.00575612	synonymous-codon	HERC1	GRCh38.p7	15:63775461	GTCCTTTGAGGCATA[A/G]AACTTGTTGGGGCAA	8925
rs756693602	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63801807	TCCACTTCAGTCTCC[C/T]CCTCTTCATGTACAT	8925
rs756699637	snp	C/T	1.66161e-05	0.00288232	synonymous-codon	HERC1	GRCh38.p7	15:63662010	TTCCCTGTCTTCAGA[C/T]TCACAAACATGCTGC	8925
rs756738284	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63667023	TGCTAAAGTGCTGTC[C/T]AGTGTTTCTAAGCAC	8925
rs756741206	in-del	-/TGA			intron-variant	HERC1	GRCh38.p7	15:63626216	TCACTTTTCACATTT[-/TGA]AAAATTTCAAGCATA	8925
rs756742443	snp	C/G	1.80088e-05	0.00300068	missense	HERC1	GRCh38.p7	15:63645579	AGTGAATGTAGACAG[C/G]ACCAGCATCCCGAAA	8925
rs756757636	snp	C/T	0.00023655	0.0108729	intron-variant	HERC1	GRCh38.p7	15:63758152	GATTATCTACCAGTT[C/T]GTAAGCTATTTAGAA	8925
rs756757680	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63636376	CCCCGGTTCAAGTGA[C/T]TCTCTTGCCTCAGCC	8925
rs756770625	snp	A/G	2.26027e-05	0.00336167	intron-variant	HERC1	GRCh38.p7	15:63633798	TAACTACTGACATAG[A/G]TGAAAACTATTTATG	8925
rs756786870	snp	C/G	5.19503e-05	0.00509632	missense	HERC1	GRCh38.p7	15:63775596	GTTCAAGCCATTTCA[C/G]CTTCACTGGTGGAAT	8925
rs756787396	snp	A/G	1.65603e-05	0.00287747	synonymous-codon	HERC1	GRCh38.p7	15:63733053	ACACACAGAAGATAG[A/G]TCAGCAGCATCAGAG	8925
rs756796869	snp	A/G	1.65974e-05	0.0028807	missense	HERC1	GRCh38.p7	15:63628728	CAGCACTGTGGCAGC[A/G]GCCAGCCGAGATCTG	8925
rs756801450	in-del	-/TAC			intron-variant	HERC1	GRCh38.p7	15:63761703	TTTTTTCAGTAATCA[-/TAC]AGCAGTAATTATTTG	8925
rs756803786	snp	A/G	3.91037e-05	0.00442158	intron-variant	HERC1	GRCh38.p7	15:63725275	TGTATTTTAAATGCT[A/G]CAGAGAAGCACATTA	8925
rs756806298	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63711447	ACTGGGAGTATGAAG[C/T]GGAAGCACAGAGATA	8925
rs756811109	in-del	-/A	0.000102777	0.00716783	intron-variant	HERC1	GRCh38.p7	15:63656364	ACTGGAACCACTGCC[-/A]GTAAAGAAAAACATC	8925
rs756816701	snp	A/C	1.66396e-05	0.00288436	missense	HERC1	GRCh38.p7	15:63616573	ACACCAGAGGGGCCA[A/C]GTGGAGGTCCAGAGG	8925
rs756817295	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63695633	CCTCAGGTGATCCGA[A/C]CACCTCAGCCTCCCA	8925
rs756823432	snp	A/T	1.65685e-05	0.00287819	missense	HERC1	GRCh38.p7	15:63698910	AATCTGACTCAAAGG[A/T]ATAGGAGGAGTTGCA	8925
rs756824267	in-del	-/TTCT			intron-variant	HERC1	GRCh38.p7	15:63644493	ATAAAGCATGTAAGC[-/TTCT]TTGTTTTTTTTTTCT	8925
rs756835715	snp	A/C/G	3.56813e-05	0.0042237	intron-variant	HERC1	GRCh38.p7	15:63675144	ATCAGAATGACACAG[A/C/G]AAGAAGCAAGTGAGG	8925
rs756836272	in-del	-/AAGA	1.66112e-05	0.00288189	intron-variant	HERC1	GRCh38.p7	15:63672716	ACCAAAAAAAAGGTT[-/AAGA]AAGTAGTAAGGATTT	8925
rs756865580	snp	A/G	3.02586e-05	0.00388952	intron-variant	HERC1	GRCh38.p7	15:63694289	ACTTCATACAGTTCT[A/G]CAAAGACATCTACCA	8925
rs756867688	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63771287	ACAAATATATAATTC[A/G]GTTTAATAAGCATTC	8925
rs756878206	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63738583	AGAAGAAAATTCAGA[G/T]AGGGTCAAAGGAAAA	8925
rs756890803	snp	C/T	1.65589e-05	0.00287736	missense	HERC1	GRCh38.p7	15:63661882	TCCACATAGGAACCA[C/T]TGCTGCGATAGCCCT	8925
rs756896214	snp	C/T	0.000100786	0.00709809	intron-variant	HERC1	GRCh38.p7	15:63680051	AATAACAAATATTCT[C/T]AAATAAAGGTTTGAG	8925
rs756900880	snp	A/C/T	4.2633e-05	0.00461678	intron-variant	HERC1	GRCh38.p7	15:63645465	ACTAAGACGTATAGA[A/C/T]GCAAATTGACAACAT	8925
rs756905760	in-del	-/G			intron-variant	HERC1	GRCh38.p7	15:63793104	TTTCACGCCCTCTCT[-/G]GGGATGCCACCCTCC	8925
rs756908865	snp	G/T	1.65671e-05	0.00287807	missense	HERC1	GRCh38.p7	15:63733001	GATGGCAGCTCTGAG[G/T]GCCGTAAGGTTGATC	8925
rs756911591	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63783301	TCCCAACCTTTCAGC[A/G]ACCCCCATCCCGATC	8925
rs756920435	snp	C/T			missense	HERC1	GRCh38.p7	15:63634824	CGACCATAGTCACCA[C/T]TCCCAAAGGTGAACA	8925
rs756936203	snp	A/T	1.65616e-05	0.00287759	missense	HERC1	GRCh38.p7	15:63669605	CCTCCTTCCTACTTC[A/T]TCAGAAGGAGAGGTT	8925
rs756948741	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63723403	ATCATAAATTTTGGT[A/G]CTACAGATAAAATCT	8925
rs756959428	snp	A/T	1.65655e-05	0.00287793	missense	HERC1	GRCh38.p7	15:63654151	CCAATTTGATAAAGG[A/T]GCATTTTCTAAGATC	8925
rs756964258	snp	A/G	1.66788e-05	0.00288775	synonymous-codon	HERC1	GRCh38.p7	15:63651359	ACTGGGTGATCCCAG[A/G]CTTTCCTCAGCATCC	8925
rs756986650	snp	A/T	1.66018e-05	0.00288108	synonymous-codon	HERC1	GRCh38.p7	15:63749405	TGCCAGACTATGTGA[A/T]GTTCCAGCCGAAATC	8925
rs757008357	snp	C/T	1.6591e-05	0.00288015	missense	HERC1	GRCh38.p7	15:63648139	AGTAACAGTTTTCCA[C/T]CAAAATATCCCACTG	8925
rs757016729	snp	C/T	1.67416e-05	0.00289318	intron-variant	HERC1	GRCh38.p7	15:63754490	AAAGCTACTGATAAA[C/T]AATTTTTTACATACC	8925
rs757032556	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63610927	TAAGTTCTGGGTTTG[A/C]GGGCTGTACCCAGTG	8925
rs757036287	snp	A/C	5.23136e-05	0.0051141	missense	HERC1	GRCh38.p7	15:63713594	GAGCCCCAGACCCTG[A/C]CCCACTGTTCATTCT	8925
rs757036418	snp	A/T	4.13676e-05	0.00454776	intron-variant	HERC1	GRCh38.p7	15:63694907	ATCCTGAATTACACA[A/T]AAAGAATTACTTTTT	8925
rs757044522	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63752212	TATATGCTGATTTCA[A/G]CTTTTCTGCTCCTCT	8925
rs757056299	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63711734	CTCTATGAGCTGTCA[C/T]ATGATATGACCAAGA	8925
rs757059643	snp	C/T	3.15542e-05	0.00397191	intron-variant	HERC1	GRCh38.p7	15:63758398	AAAATATGCAACAAA[C/T]AGTCAAGACAGTTTT	8925
rs757074206	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63736916	CCGGCCATAGCATCA[C/T]ACTCTTACCCATGAT	8925
rs757076215	snp	A/G	8.71979e-05	0.00660237	intron-variant	HERC1	GRCh38.p7	15:63749599	AAATGTAATATATTT[A/G]CACAAGACAACAGTT	8925
rs757079331	snp	A/G	0.00015873	0.00890729	intron-variant	HERC1	GRCh38.p7	15:63625918	GCCCTGGGGCCTGGC[A/G]AGCATGTCACGGGCA	8925
rs757087642	snp	A/C	1.92406e-05	0.0031016	missense	HERC1	GRCh38.p7	15:63696140	TGATAGTGATGCAAT[A/C]GGCCACTCTCTCCCT	8925
rs757095410	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63750365	CAAAAGAATCACTAA[C/G]TGATTTAAGATGCTT	8925
rs757096809	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63704362	GACCTGGTTAACACA[G/T]ACTGAATCTCAAATT	8925
rs757099351	snp	C/G	1.65743e-05	0.00287869	missense	HERC1	GRCh38.p7	15:63725359	CCAATATGCAGTGTC[C/G]TGTTCCTCTGGAGAC	8925
rs757120563	snp	A/T	1.91214e-05	0.00309198	missense	HERC1	GRCh38.p7	15:63729257	ATTTTTCTCCAACAC[A/T]GCCATTCCAAGGACT	8925
rs757120736	snp	C/G	1.82884e-05	0.00302388	missense	HERC1	GRCh38.p7	15:63643451	GTCCACCAGACACCA[C/G]GGCCAACCCATCAGA	8925
rs757122173	snp	A/G	0.000132512	0.00813869	synonymous-codon	HERC1	GRCh38.p7	15:63713475	TAACAGGGCACACCG[A/G]TGGATCACGGAGTTG	8925
rs757123701	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63793855	TGGGTAAAATGAGGC[C/T]GAGACCTACTGGGCT	8925
rs757125002	snp	C/T			missense	HERC1	GRCh38.p7	15:63725427	CAATAAGGAGAGCAA[C/T]TGTTCTTTCTAGATC	8925
rs757129493	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63794644	AGGAGACATGAGGAA[C/G]ACCAAATATATATTT	8925
rs757141322	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63658780	TACATCTGAACTACT[A/G]AAAACATTTCCTATT	8925
rs757146168	snp	C/T	1.66696e-05	0.00288696	missense	HERC1	GRCh38.p7	15:63674716	TGGTTTTTGGACATG[C/T]GTTCATGATTTTTTC	8925
rs757149876	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63717184	CTTTTACAGAGATGG[C/G]GATACAGAGTAGTCA	8925
rs757178884	snp	C/T	3.31334e-05	0.00407009	missense	HERC1	GRCh38.p7	15:63758231	GTATTTTCTCCTGTG[C/T]ACCTTCTACCAACTG	8925
rs757188085	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63781427	ATTTCAAACTTTTCA[C/T]TATTATTATAACTGT	8925
rs757191223	snp	C/T	1.69818e-05	0.00291387	missense	HERC1	GRCh38.p7	15:63656350	GCAGCCAGGCTACAA[C/T]TGGAACCACTGCCAG	8925
rs757197667	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63627548	GCGTGGTGGCACATG[C/G]CTGTAATCCCAGCTA	8925
rs757200906	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63804813	CCAAAGATACATAAA[C/T]AGCCAAAAAAGCGCA	8925
rs757201144	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63683527	GATGACTTTCTAGCC[G/T]AAGTACATATTTCTG	8925
rs757201379	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63716049	TTCATTTCATGATGA[A/G]GCTCAGTGAAGCAGG	8925
rs757202008	in-del	-/C	1.65795e-05	0.00287914	frameshift-variant	HERC1	GRCh38.p7	15:63752961	CCTTAGTCCTACCTG[-/C]CCTGTTGATGTCAAA	8925
rs757210641	snp	C/T	6.93686e-05	0.00588893	missense, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609175	TTGTTGATGGCATAG[C/T]GCAGGCGCTCGGCCA	8925
rs757219034	snp	C/T	5.2744e-05	0.0051351	missense	HERC1	GRCh38.p7	15:63656215	TGCCCACCTCGTGAT[C/T]GTTCTGAGGTGCTAG	8925
rs757219350	snp	A/G	0.000132534	0.00813937	synonymous-codon	HERC1	GRCh38.p7	15:63756527	ATCACCATCTCCCCA[A/G]CTGAAGACTTCTCCT	8925
rs757221928	snp	C/G/T	0.00011599	0.00761464	synonymous-codon	HERC1	GRCh38.p7	15:63775126	CGCAAATAATAAACT[C/G/T]AGACCAGTTCGAACA	8925
rs757233265	snp	C/G/T			intron-variant	HERC1	GRCh38.p7	15:63671567	AATTCTCAAAGTGTA[C/G/T]GCTGAAGCCACTGTA	8925
rs757253228	snp	A/G	5.03132e-05	0.00501538	intron-variant	HERC1	GRCh38.p7	15:63633992	AAATAACAGCATTCC[A/G]TAAGGCAAATCACAA	8925
rs757267481	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63762208	GTTAAAATAACTTAG[G/T]AACCACCCTGAAGAG	8925
rs757271641	snp	C/T	1.6906e-05	0.00290736	missense	HERC1	GRCh38.p7	15:63755238	TCTTACCTAATCTTC[C/T]AAAGTCTCCTTCACC	8925
rs757278763	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63742115	AGTCTTGCAATCCAT[-/A]AACATGAGGTGTGTT	8925
rs757303666	snp	A/C	1.65679e-05	0.00287814	missense	HERC1	GRCh38.p7	15:63630510	ACACATCTCCATTTG[A/C]TGCCAAAGCAAGTGT	8925
rs757314378	snp	A/C	1.68335e-05	0.00290111	intron-variant	HERC1	GRCh38.p7	15:63651233	TTTCAGCAGTTTACT[A/C]GTGTTTACATGACTC	8925
rs757326445	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63670669	TGCCCACACTAATCA[C/G]AGCTGAAAAGGTTAC	8925
rs757330367	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63815258	TAATTTATATTTCAC[A/G]CTCTCCACCTTCCAT	8925
rs757341155	snp	C/T	1.65781e-05	0.00287902	synonymous-codon	HERC1	GRCh38.p7	15:63678096	TTCCTCTTTGCTCTC[C/T]TTCTCCTCTCTCATT	8925
rs757354463	in-del	-/AGG			intron-variant	HERC1	GRCh38.p7	15:63611331	TCTGAAAGGTCTAAA[-/AGG]AGGAGAGTGACATGG	8925
rs757362656	snp	C/T	1.73667e-05	0.0029467	intron-variant	HERC1	GRCh38.p7	15:63755357	TAAATACGATGAGTA[C/T]GCACATGTTAAAACA	8925
rs757363533	in-del	-/ACAC			intron-variant	HERC1	GRCh38.p7	15:63813312	GATAATCAGAGATGG[-/ACAC]ACACACACACACACA	8925
rs757379778	snp	A/G	1.73963e-05	0.00294921	intron-variant	HERC1	GRCh38.p7	15:63718743	ATTTCTGACATCATG[A/G]GAGCAAATATTTGTC	8925
rs757379786	snp	C/G	1.65751e-05	0.00287876	synonymous-codon	HERC1	GRCh38.p7	15:63638507	AGCACCCCATAAGTA[C/G]ACATCACATTTACCT	8925
rs757415004	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63651388	CCCCTTCCCTAGAAT[A/G]TAACAGACAGATATG	8925
rs757424388	snp	A/G	1.76749e-05	0.00297273	missense	HERC1	GRCh38.p7	15:63696236	GTGAGTAGTGTGGAG[A/G]ACTGGAAGCCTGAAC	8925
rs757427256	snp	A/G	3.38828e-05	0.00411585	intron-variant	HERC1	GRCh38.p7	15:63690679	CTTTTCTTATTATCA[A/G]TGTGACTTAAATTCA	8925
rs757443981	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63728320	TTTTAAAAATCAAGA[C/T]CACCTTAAATCATGT	8925
rs757446033	snp	C/T	1.7968e-05	0.00299728	missense	HERC1	GRCh38.p7	15:63615790	TCCATCTCATGAAGT[C/T]GATATTCAATGGCCC	8925
rs757452335	snp	G/T	6.21253e-05	0.00557304	missense	HERC1	GRCh38.p7	15:63694020	TTTTTTTCTTCTTCT[G/T]CACCGTCTTCTTGCT	8925
rs757452947	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63814506	GCTCTGCTGCCCATG[C/T]TGGAGTGCAGTGACA	8925
rs757455088	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63827974	ACTGGGAAGCGGACC[C/T]GGGAAGTGACTGCTA	8925
rs757467524	snp	C/T	1.6563e-05	0.00287771	intron-variant	HERC1	GRCh38.p7	15:63718947	GGCTCAGAAAACAGT[C/T]CAGAGGTAATTTTTA	8925
rs757472599	snp	C/T	1.65999e-05	0.00288091	synonymous-codon	HERC1	GRCh38.p7	15:63666083	CTCTTCATCCTCATG[C/T]CCAGGGTGCTCTATC	8925
rs757476736	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63785808	AGGGGAAGGGGAAGG[A/G]AAGGGAAATTGGTAA	8925
rs757493748	snp	C/G/T	3.37777e-05	0.00410949	intron-variant	HERC1	GRCh38.p7	15:63660929	TAAGCAGAGAGGATA[C/G/T]ATAAAAAAACATGTA	8925
rs757497283	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63664168	TTAAACATGCATCAT[C/T]ACTTCTTAAATTATA	8925
rs757501590	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63756378	AAAATCTGAACGACA[C/T]TGTCAATTACAACTC	8925
rs757504649	snp	A/G	1.68895e-05	0.00290593	intron-variant	HERC1	GRCh38.p7	15:63729417	TGAAAGATTCAAGGT[A/G]TAAAAATATCATGGC	8925
rs757505613	snp	A/T	1.65644e-05	0.00287783	missense	HERC1	GRCh38.p7	15:63677941	CGCCCAGTTTGCTTG[A/T]GAACACACCGACCTC	8925
rs757507167	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63663430	GATAGGTTTAAGTAA[A/G]AGAATCCATGCGATG	8925
rs757510063	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63827036	TACCAAAATACTACG[C/T]GCAAGGCTATTTACA	8925
rs757510326	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63742961	TTCTTGCAATGTTTT[C/G]GTCCACAATTAGGGT	8925
rs757512373	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63641418	AAGGCTATAATCACA[C/T]TCCAAAGCACCAGGT	8925
rs757514803	in-del	-/CCAA	1.66362e-05	0.00288406	frameshift-variant	HERC1	GRCh38.p7	15:63616570	TCCACACCAGAGGGG[-/CCAA]GTGGAGGTCCAGAGG	8925
rs757520941	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63638820	ATTCTGCTTAGGCAA[A/G]ATGCACCTGCTCTTA	8925
rs757523877	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63632609	ACTACTCACCACCTA[A/G]AACAAAAAAAGGACT	8925
rs757535071	in-del	-/TTT			intron-variant	HERC1	GRCh38.p7	15:63701999	AAATCCAACAAAAAA[-/TTT]TTGAGATTGTTTACT	8925
rs757562043	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63741910	GTATGTTTTGAAGTT[C/G]GAAAGTGTGAGCCTT	8925
rs757569399	snp	G/T	1.65647e-05	0.00287786	missense	HERC1	GRCh38.p7	15:63775030	CAAAGAGCTCACAAC[G/T]TCAATTGCAGTATGA	8925
rs757569677	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63804857	AACACCATTAGTCAG[C/T]AGGGAAATGGAAATT	8925
rs757570114	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63615010	GAGATGCCCTCTTAG[C/G]TGAGGCTTAAAGAAC	8925
rs757573089	snp	C/T	6.46475e-05	0.00568503	intron-variant	HERC1	GRCh38.p7	15:63727606	CAAGAGGAACAACTT[C/T]TCTCAAAGGCATTAT	8925
rs757585823	snp	A/C/T	8.54218e-05	0.00653486	intron-variant	HERC1	GRCh38.p7	15:63658537	TGTGACATAAAATAA[A/C/T]ACTTACCTGACTGAG	8925
rs757587440	snp	A/G	2.59676e-05	0.00360321	intron-variant	HERC1	GRCh38.p7	15:63764194	CAGCAGATGAACCCT[A/G]TAATTAAAACATTGC	8925
rs757594239	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63721712	AAAAAATGGACAAAA[C/G]TAATGACAGGATAAG	8925
rs757596189	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63707860	CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG	8925
rs757600125	snp	C/G	1.76858e-05	0.00297365	intron-variant	HERC1	GRCh38.p7	15:63641444	CAGGTATCTGTGTAT[C/G]TCTAGGAGTGAGTGT	8925
rs757609193	snp	A/T	1.67267e-05	0.0028919	intron-variant	HERC1	GRCh38.p7	15:63638398	CTTTTCTATTTTTTA[A/T]CCTGTTAGTTACCTG	8925
rs757611030	snp	G/T	1.72779e-05	0.00293916	intron-variant	HERC1	GRCh38.p7	15:63643567	TGAAATTCATTATTT[G/T]TAACATGCATTAAAA	8925
rs757611707	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63646132	CTGTGATCATTGTGC[G/T]CTTCTGATTTTATTT	8925
rs757624670	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63633317	CTGCTTGTGAAATAC[A/G]TCAGGAAAACCCACA	8925
rs757626327	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63768490	TGCTACAACAACAAA[C/T]ACTTGGTTGCAACCT	8925
rs757632644	snp	A/G	1.65996e-05	0.00288089	synonymous-codon	HERC1	GRCh38.p7	15:63623830	CAGGCGGAGGTCTGA[A/G]GCATTCAGCTTAACT	8925
rs757634346	snp	A/C	1.70162e-05	0.00291682	intron-variant	HERC1	GRCh38.p7	15:63622937	AATGACAATCAAATG[A/C]ATGAAGAGAACAAAC	8925
rs757634958	snp	A/G	1.65655e-05	0.00287793	synonymous-codon	HERC1	GRCh38.p7	15:63725485	CTGAGGTAATGGCAG[A/G]CCAGCAGGATCAATT	8925
rs757639744	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63676382	AAGTTTATGTGTATG[A/T]ATTTTTTGGCTAAGA	8925
rs757639946	snp	A/G	1.65897e-05	0.00288003	synonymous-codon	HERC1	GRCh38.p7	15:63664531	TCTTGTTACCGCTGA[A/G]CGACCTCTAGCTGAT	8925
rs757642287	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63737286	GTATCCCAATAATAA[A/G]GAGTTCCAGAGAGAA	8925
rs757655603	snp	C/T	1.65701e-05	0.00287833	missense	HERC1	GRCh38.p7	15:63612363	TCCTCATTGGAGAAC[C/T]CTTCCAGCGTGTGCC	8925
rs757660008	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63613413	TATTATACAGTAGTG[C/T]ATACCCTACACACAG	8925
rs757665006	snp	C/T	1.66394e-05	0.00288434	missense	HERC1	GRCh38.p7	15:63694441	TCTGTACCACACAAC[C/T]GTGACAATACGTTTA	8925
rs757686152	snp	G/T	1.6563e-05	0.00287771	missense	HERC1	GRCh38.p7	15:63686462	TCCACTAGGCAACAC[G/T]GAGCTTTCTCCGGGT	8925
rs757705061	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63808566	GCTGGAATTACAGGC[A/G]TGAGCCACTGTACAC	8925
rs757705293	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63797579	TTCCCTAGTCCCCCA[C/T]CCATCAAACTATCCT	8925
rs757719245	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63720657	GATTTTAAGAAATTC[C/T]TAAAGCCCACAGAGA	8925
rs757727800	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63675627	ATAACTTATTTCAGT[A/G]AGGACTTCATTTCAT	8925
rs757731394	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63803317	GTCACAACTGCCAGT[A/C]ATTGATAGAGTAAGG	8925
rs757745102	snp	A/C/G	3.37218e-05	0.00410609	missense	HERC1	GRCh38.p7	15:63712830	TCAGATTCACTCCTC[A/C/G]ATTTGATCAGTCTAT	8925
rs757749585	snp	A/G	2.29066e-05	0.0033842	stop-gained	HERC1	GRCh38.p7	15:63655874	CTTCAGCAATTCCTC[A/G]GAGAAAGCTGGGTAG	8925
rs757750709	snp	A/G	1.6633e-05	0.00288378	synonymous-codon	HERC1	GRCh38.p7	15:63640413	TTGCATATAGGGGCT[A/G]TGAACAAGTTGGTCA	8925
rs757760612	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63717947	TCAGAAAGCCTATTT[C/T]CCTAACATTCAGCTA	8925
rs757762925	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63825609	TTATTTTGTAATCAG[G/T]AAAATGAAGTATTAT	8925
rs757782637	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63779798	AGGTGGGAGGATCAC[A/G]AGGTCAAGAGATGGA	8925
rs757800324	snp	A/G	1.69642e-05	0.00291236	intron-variant	HERC1	GRCh38.p7	15:63694567	AAAAGACAAAGAGAC[A/G]GTTAAGAATCTTCCT	8925
rs757806758	snp	A/G	1.6582e-05	0.00287936	missense	HERC1	GRCh38.p7	15:63756549	ACTTCTCCTTCTGTC[A/G]TAAAGGCTAAAGTGT	8925
rs757807498	snp	A/G	1.89349e-05	0.00307686	missense	HERC1	GRCh38.p7	15:63672643	GGGCTAGTAGTAACT[A/G]GTGTCTGTGCCTGCT	8925
rs757808751	snp	A/T	2.19008e-05	0.00330906	intron-variant	HERC1	GRCh38.p7	15:63734872	CAAAAGAGAAAAGTA[A/T]ACTGATTGGCCTGGT	8925
rs757816023	snp	C/T	6.71299e-05	0.00579314	intron-variant	HERC1	GRCh38.p7	15:63634010	AGGCAAATCACAAGA[C/T]CTAAAACACACTCCC	8925
rs757824815	snp	A/T	2.47816e-05	0.00351997	intron-variant	HERC1	GRCh38.p7	15:63649693	AAGGAAGTTGGAGAC[A/T]CCGTCAGCTAGACGT	8925
rs757834371	snp	C/T	1.73963e-05	0.00294921	missense, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609185	CATAGCGCAGGCGCT[C/T]GGCCATGACCAGCTG	8925
rs757835326	snp	A/G	1.71566e-05	0.00292883	intron-variant	HERC1	GRCh38.p7	15:63656364	ACTGGAACCACTGCC[A/G]GTAAAGAAAAACATC	8925
rs757835766	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63778589	GGCAAAATAGACCCA[C/T]AAAATTGAAGACAGA	8925
rs757837543	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63655552	AATCATAATCTATAA[C/G]TAAACTAATATGGTA	8925
rs757843565	snp	A/G	1.65723e-05	0.00287852	synonymous-codon	HERC1	GRCh38.p7	15:63758259	CTGATGGCTGCTATT[A/G]CTCCCCCAAACATAA	8925
rs757851511	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63700521	AGGATTTCAAAATTC[A/G]TAACACGGAGCTAAT	8925
rs757861161	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63699223	AAAGCCCTGTTTGAT[A/G]TACCAGTGTCTCTGT	8925
rs757861329	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63648540	TCTACCATGAAACTG[A/G]GAAGTGAAAGAACCC	8925
rs757868559	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63741152	TTCTGCCCCAGCCTC[A/C]CAAGTAGCTGGGATT	8925
rs757870895	snp	C/T	1.70679e-05	0.00292124	intron-variant	HERC1	GRCh38.p7	15:63674339	AAAAATCAGATAACA[C/T]ACCTTGCTTAATTTT	8925
rs757871033	snp	C/T	1.68522e-05	0.00290272	intron-variant	HERC1	GRCh38.p7	15:63663239	GGCATTTTATTTGCA[C/T]GCATAAAATAATTCT	8925
rs757882249	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63819809	CCCCGCTAGTCTCCA[C/T]CAACATTTTTTCATT	8925
rs757889726	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63623615	TATGAGGCTCACAAA[C/T]GCATCCTTGCTACAT	8925
rs757911960	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63710414	AGGAAAAAACCAAAT[A/G]CATGTGGAAATTTTG	8925
rs757922936	snp	A/G			missense	HERC1	GRCh38.p7	15:63649769	CGACGGTGCATGGTG[A/G]ACACATCAACAACTT	8925
rs757927373	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63654644	GATCACCTGAGGTCA[C/G]GAGTTCGAGACCAGC	8925
rs757927407	snp	C/T	3.33522e-05	0.0040835	missense	HERC1	GRCh38.p7	15:63624291	GTTGTCCCTGTACAA[C/T]GCCCCAAGTTCCAGC	8925
rs757933472	snp	A/G	1.67293e-05	0.00289212	intron-variant	HERC1	GRCh38.p7	15:63758414	AGTCAAGACAGTTTT[A/G]GTCTGGGCATTTTTT	8925
rs757943583	snp	C/T	1.85972e-05	0.0030493	missense	HERC1	GRCh38.p7	15:63713609	CCCCACTGTTCATTC[C/T]ATCTCGGTCTCGGCT	8925
rs757943927	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63738037	CTACTGATGGATGAA[A/G]AAACCCAGCAGAAAC	8925
rs757944682	snp	A/G	2.73669e-05	0.00369901	intron-variant	HERC1	GRCh38.p7	15:63694301	TCTACAAAGACATCT[A/G]CCATACTTACCCAGT	8925
rs757945370	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63713890	GAAATACTAATCTGC[C/T]TTTACAGAATTTTAA	8925
rs757951710	snp	A/G	1.79245e-05	0.00299365	missense	HERC1	GRCh38.p7	15:63634788	GGAAGTTTTTTGTTA[A/G]AGGTATTTCCAAGAC	8925
rs757952890	snp	C/T	3.38977e-05	0.00411676	intron-variant	HERC1	GRCh38.p7	15:63672453	CTGTGCCTTCAGAAA[C/T]ACAGGCATCAGTATG	8925
rs757953215	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63801897	AGTCAAAACTTCTCC[C/T]GAGCTCCAGACCTGG	8925
rs757959093	snp	C/G			missense	HERC1	GRCh38.p7	15:63680728	CTGGCCAGCGAGAAA[C/G]TCCAACACACGTGCC	8925
rs757959275	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63821891	TTCATGGAGTTTACA[C/T]TCTAGTAAGGAAGAC	8925
rs757980910	in-del	-/AT			intron-variant	HERC1	GRCh38.p7	15:63653638	GTATCTGCATAGAAC[-/AT]ATATATATATCCTCC	8925
rs757981190	snp	C/T	3.31329e-05	0.00407005	missense	HERC1	GRCh38.p7	15:63725376	GTTCCTCTGGAGACA[C/T]AGGGGAGCCCTGAAG	8925
rs757981512	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63830461	GGAACTGTCAGAGAT[G/T]GGAGGAAATGAAGAA	8925
rs757988514	snp	A/C	1.65872e-05	0.00287981	missense	HERC1	GRCh38.p7	15:63680767	CTCTGTTTTCCTTCA[A/C]AATATAAAACTAAAA	8925
rs757988699	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63735026	GACTATGAATACATA[A/T]TTTCGATTTGCCACT	8925
rs757997651	snp	A/C	0.000132553	0.00813997	synonymous-codon	HERC1	GRCh38.p7	15:63725443	TGTTCTTTCTAGATC[A/C]ACAAGCCATACCCAG	8925
rs757999962	snp	A/G	1.65756e-05	0.00287881	synonymous-codon	HERC1	GRCh38.p7	15:63680576	GGTCCTGGCTTCCAT[A/G]TCTAACACACAGGTA	8925
rs758017462	snp	G/T	1.66944e-05	0.0028891	splice-acceptor-variant	HERC1	GRCh38.p7	15:63662023	GACTCACAAACATGC[G/T]GCACAAAAGGATTTC	8925
rs758045199	snp	A/G	4.96824e-05	0.00498385	synonymous-codon	HERC1	GRCh38.p7	15:63640287	TAACCAGGCCCATTC[A/G]TTTGGATTCCAGGAT	8925
rs758046515	snp	C/T	1.66546e-05	0.00288566	missense	HERC1	GRCh38.p7	15:63674725	GACATGTGTTCATGA[C/T]TTTTTCTTTTCCCTT	8925
rs758066455	snp	A/T	1.65638e-05	0.00287778	missense	HERC1	GRCh38.p7	15:63663061	GGTCTTGTCCAAACA[A/T]AGCTTCCATCGCCTC	8925
rs758066865	snp	C/T	1.73234e-05	0.00294302	synonymous-codon, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609114	GCCCTCGGCGTTGTC[C/T]ACGTTTCTCGAGAGC	8925
rs758078767	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63762247	CCAAAAATGAAACAA[A/C]ATGACCTTCACTGCA	8925
rs758081119	in-del	-/A	1.74961e-05	0.00295766	intron-variant	HERC1	GRCh38.p7	15:63686318	GGAAAAAAAAGGACT[-/A]AAAAGACAAAATGCT	8925
rs758082345	snp	A/G/T	3.34137e-05	0.00408729	missense	HERC1	GRCh38.p7	15:63694394	AAACACCCGTCTTTG[A/G/T]CAACAACTGCAGGGG	8925
rs758103460	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63726044	TGGAGTGCAGTGGCA[G/T]GATCTTGGGTCACTG	8925
rs758110092	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63637316	ATTCTAGCATTGCTA[C/T]AAGTAACCTGCAATA	8925
rs758110581	snp	A/C	1.81562e-05	0.00301294	missense	HERC1	GRCh38.p7	15:63696273	TGCTTCCTGCCAGTG[A/C]GATGCTACCTTTTTC	8925
rs758120518	snp	A/G	1.66175e-05	0.00288244	intron-variant	HERC1	GRCh38.p7	15:63729456	ATATCTGAGTTTCAA[A/G]GTCCCTGATAGATCA	8925
rs758152739	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63773178	CCGGGTGTGGTGGCT[C/G]ACACCTGTAATCCCA	8925
rs758152789	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63759440	ACCCAGAGTGGCCAT[C/G]CCAGTACCAATTTCA	8925
rs758154285	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63740415	AGTTTTTGTGTGGAC[A/G]TATGTTTTCAATGCT	8925
rs758159891	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63800995	AACGATTTAATCAAC[C/G]AAGCCTACGTAATGC	8925
rs758160641	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63729942	AGGCAGGAGAATTGC[-/T]TGAACCCCAGGAGGC	8925
rs758167919	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63750963	AAAATGAGAACATAT[A/G]TTTGTACTTGTTTCC	8925
rs758175505	snp	C/T	1.66402e-05	0.00288441	intron-variant	HERC1	GRCh38.p7	15:63733188	AACTAGCGTAATATG[C/T]ACTAGAAAAGAACAC	8925
rs758180218	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63724587	ACATGTTGAGTCTCT[C/T]TGTCTTATCAGAGAA	8925
rs758183233	snp	A/G	1.91551e-05	0.0030947	intron-variant	HERC1	GRCh38.p7	15:63752868	AAAATGTATTTATTT[A/G]AACTTTAAAATTTAA	8925
rs758200274	snp	A/G	3.51834e-05	0.0041941	intron-variant	HERC1	GRCh38.p7	15:63713697	AAAAACAAGGTCTTA[A/G]CACATGGGGAGAGAA	8925
rs758202158	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63636511	CCTGACCTCAAGTGA[C/T]CCGCCCACCTCGGCC	8925
rs758214000	snp	C/T	1.66693e-05	0.00288693	intron-variant	HERC1	GRCh38.p7	15:63666330	TCTCATATCTGTATA[C/T]ACTGATATATAAAAA	8925
rs758219390	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63690745	GGCTGCTAAACATTT[A/G]TGGGTGGAACAAACT	8925
rs758222918	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63689778	CTGTATCATGTTAAC[A/T]GTAATATTAACTCGC	8925
rs758223538	snp	A/C	4.98103e-05	0.00499026	synonymous-codon	HERC1	GRCh38.p7	15:63729602	TGATGATGATGTTCC[A/C]AGTAGAAATTTATCA	8925
rs758228219	snp	A/G	1.73171e-05	0.00294249	intron-variant	HERC1	GRCh38.p7	15:63690697	TGACTTAAATTCAAA[A/G]TTAAAATGAACTTCT	8925
rs758233555	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63661161	TGTTTCATGTTATAG[A/G]CTAACATAATAAAAA	8925
rs758237039	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63659997	ACATAAATCTGCTGG[C/T]AATGGTTGTTCTGAA	8925
rs758237813	snp	C/G	1.65715e-05	0.00287845	missense	HERC1	GRCh38.p7	15:63775130	AATAATAAACTTAGA[C/G]CAGTTCGAACACCCA	8925
rs758238906	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63663873	TCTCTCACTGTTCCT[A/G]TAAATTACTGAATCA	8925
rs758269689	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63752280	GCCTGACACAAGGTG[G/T]CCTCCTATACATGAC	8925
rs758277571	snp	C/G	1.65968e-05	0.00288065	missense	HERC1	GRCh38.p7	15:63718785	TTAAGTTACTTGCCG[C/G]CTTTCTCCACATGCT	8925
rs758279238	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63739063	TCAATGGTTTTTAGT[C/T]TATTCAGAGTTGTGC	8925
rs758280388	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63783310	TTCAGCAACCCCCAT[C/T]CCGATCAGTCAGCAG	8925
rs758281746	snp	A/G	1.658e-05	0.00287919	synonymous-codon	HERC1	GRCh38.p7	15:63638519	GTAGACATCACATTT[A/G]CCTCCCAGGTGCCAG	8925
rs758292696	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63687372	GTGAAACCCCGTCTC[C/T]ACTAAAAATACAAAA	8925
rs758303265	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63753927	GCCTGTAATACAAGC[A/T]CTTTGGGAGACTAAA	8925
rs758306461	snp	C/T	3.65344e-05	0.00427386	intron-variant	HERC1	GRCh38.p7	15:63652404	GTATACACGTGATGT[C/T]AGCACTCACAATCTG	8925
rs758309956	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63833605	CAGGAGGCCTCTAGA[A/G]CCGGGGACCCGGGGG	8925
rs758316653	snp	C/T	3.28413e-05	0.0040521	intron-variant	HERC1	GRCh38.p7	15:63749641	CTTAAAAACAAATGA[C/T]TTTACCATGAGAAAG	8925
rs758317894	snp	A/G	3.49993e-05	0.00418311	intron-variant	HERC1	GRCh38.p7	15:63658521	AGTTAACTTAGCATC[A/G]TGTGACATAAAATAA	8925
rs758331601	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63795740	CCGAACAAAAGAGAC[-/A]AGGGTCATTTATAAT	8925
rs758348581	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63610990	TCTGCCTTCAGCAAT[A/G]GTAGGGGCACTCCTG	8925
rs758348720	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63630116	CTAATCTCACATCTT[A/G]CTGTAGTAATGATGA	8925
rs758350962	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63706171	AACCATGAGTTAACT[A/G]TACTATTCATTAACA	8925
rs758366183	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63794925	ACAAAAATTAGCCAG[G/T]CGTGGTGGTGTGTAC	8925
rs758370870	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63627811	CCCACAGTTGGGTGT[C/T]GAGCACACAAGTATG	8925
rs758393126	snp	A/G	1.66076e-05	0.00288158	synonymous-codon	HERC1	GRCh38.p7	15:63756566	AAAGGCTAAAGTGTG[A/G]CCATCAGATCCTTTA	8925
rs758408809	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63824218	AACCGCCATTATGGA[A/G]AACAGTATGTAGGTT	8925
rs758410024	snp	A/C	1.88326e-05	0.00306854	missense	HERC1	GRCh38.p7	15:63643463	CCAGGGCCAACCCAT[A/C]AGAACTAAAGGCAAC	8925
rs758416107	in-del	-/TATT			intron-variant	HERC1	GRCh38.p7	15:63693416	CCAGGCTAATTTTCA[-/TATT]TATTTTTAGTAGAGA	8925
rs758418945	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63800516	GTACAGTACCAGAGA[-/T]TATTAATTAGGTACT	8925
rs758432951	snp	C/T	2.45534e-05	0.00350373	intron-variant	HERC1	GRCh38.p7	15:63649698	AGTTGGAGACTCCGT[C/T]AGCTAGACGTAAGTG	8925
rs758440166	snp	A/C	1.66277e-05	0.00288333	missense	HERC1	GRCh38.p7	15:63623846	GCATTCAGCTTAACT[A/C]CTTGTCTCGCTATTT	8925
rs758443726	snp	A/C	1.66629e-05	0.00288638	missense	HERC1	GRCh38.p7	15:63666098	CCCAGGGTGCTCTAT[A/C]ATCCACATGGCAAGG	8925
rs758468506	snp	C/T	1.66629e-05	0.00288638	missense	HERC1	GRCh38.p7	15:63674369	TGCCCCCAAACTGGT[C/T]TTCCAAAAGCCCATG	8925
rs758474410	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63704897	GCGCCCACCACCACG[C/T]CCGGCTAATTTTTTG	8925
rs758475591	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63684795	GGTGGATCACCTGAG[A/G]TCAGGAGTTCCAGAT	8925
rs758515350	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63828374	GACAAAGTTTTGCTC[C/T]TGTTGCCCAGGCTGC	8925
rs758525848	in-del	-/CTTAG			intron-variant	HERC1	GRCh38.p7	15:63820153	AAATACATGAAACTT[-/CTTAG]AACAGTGACTGCACA	8925
rs758529348	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63717330	AAATACTAAGTCAGT[A/T]TATGACAAAAGTCTA	8925
rs758538480	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63671730	TGAGAATCACTACAA[A/T]AGACACTCCCCTGTT	8925
rs758543608	snp	A/C	1.6867e-05	0.002904	missense	HERC1	GRCh38.p7	15:63712839	CTCCTCGATTTGATC[A/C]GTCTATAATTTGGGC	8925
rs758546456	snp	C/T	0.000302115	0.0122868	missense	HERC1	GRCh38.p7	15:63655768	ACTTCTGACTTATCA[C/T]AGTTAGGTCTTAGTT	8925
rs758546509	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63640630	TTTCTGTATACCCTT[A/C]GCCCAACTTTATCCA	8925
rs758554846	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63742872	TAGTTTGTTGAGAAT[A/T]TTTACATCTATCTTC	8925
rs758563546	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63697737	TGGGATTACAGGAGT[A/G]AGCCACCGCGCCCGG	8925
rs758565711	snp	C/T	1.65806e-05	0.00287924	synonymous-codon	HERC1	GRCh38.p7	15:63678105	GCTCTCCTTCTCCTC[C/T]CTCATTTCATTTTCC	8925
rs758567629	snp	A/G	1.98194e-05	0.00314791	intron-variant	HERC1	GRCh38.p7	15:63692574	AAGAGCAGCTACAGT[A/G]AAGAGACAAGTTTAC	8925
rs758569392	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63765637	ACTCTTTCAACGAAC[A/G]GCCAATCAGAATATG	8925
rs758573469	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63618812	GTCTGTTATTGGTGT[A/G]TAAGAATGTTTGTGA	8925
rs758582293	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63706955	TACTTATTCATCATT[A/C]AAGTCAAACTAATAA	8925
rs758590749	snp	C/T	1.65866e-05	0.00287976	missense	HERC1	GRCh38.p7	15:63775253	TGCTTCACCTTGCCT[C/T]TGTCATGGTATTTAT	8925
rs758596055	snp	G/T	1.7741e-05	0.00297829	intron-variant	HERC1	GRCh38.p7	15:63713316	AGTAATAAAGGGAAG[G/T]GAGTAGGTCATGTTT	8925
rs758602594	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63731133	AAATATTCCATTGAA[C/T]ACATGTACCATAAAT	8925
rs758602689	snp	G/T	3.35762e-05	0.00409719	intron-variant	HERC1	GRCh38.p7	15:63723155	GAGCTAACTACAAAT[G/T]TACTCCCTTTATCTT	8925
rs758609662	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63816924	GACATAAGACCTTAC[A/G]TATCTCCCGATGGAA	8925
rs758620080	snp	C/T	4.99114e-05	0.00499532	missense	HERC1	GRCh38.p7	15:63678232	ATGCAGTAAGTCCAA[C/T]GGTCTGTTCGGTGAA	8925
rs758639576	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63653257	ACCAGCCTGGCCAAC[A/G]TGGAAAAACCCTGTC	8925
rs758641291	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63769688	GTGAAGCCCCATCTC[C/T]ACTAAAAATATAAAA	8925
rs758643728	snp	G/T			missense	HERC1	GRCh38.p7	15:63615839	TGTTGGAAAATGTGA[G/T]TGGGATACTATTTCC	8925
rs758653487	snp	A/C	1.96624e-05	0.00313541	synonymous-codon	HERC1	GRCh38.p7	15:63672663	CTGTGCCTGCTGGGC[A/C]GGGTCACTTTCTTCA	8925
rs758657637	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63744519	TTAGAGGTCTACCCA[A/G]TGTTCTATTGTACTA	8925
rs758665948	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63776171	TTTTTATCTCCAACC[C/G]AGGCCTTCTCCCTAA	8925
rs758670223	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63833398	CGGACCCTGAGAGGG[A/T]GTCGGCCGCCGCCCG	8925
rs758680902	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63743100	CACAAGTGAAGCCAT[C/T]TGCTCCTGGGCTTTT	8925
rs758684341	snp	A/G	1.77256e-05	0.00297699	intron-variant	HERC1	GRCh38.p7	15:63756396	TCAATTACAACTCCA[A/G]TGCATCTAATTATTT	8925
rs758686593	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63828899	AAAGCAAAAATAACT[A/G]CATACAAATACACTA	8925
rs758696768	snp	C/T	0.000138904	0.00833263	missense	HERC1	GRCh38.p7	15:63655904	GAAACTTTCGCTGAA[C/T]TGAGTCATCAACTGT	8925
rs758707438	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63709851	CAACATAAGACAAAC[A/G]GTAAATTATCAGACA	8925
rs758728472	snp	A/G	1.65751e-05	0.00287876	synonymous-codon	HERC1	GRCh38.p7	15:63727786	AGGGAGTAACAGCAG[A/G]GAGTTAACAATCTGG	8925
rs758732011	in-del	-/GGCTTCTTTGTGCG	1.66557e-05	0.00288575	frameshift-variant	HERC1	GRCh38.p7	15:63616587	AAGTGGAGGTCCAGA[-/GGCTTCTTTGTGCG]AATGGCAACCCCCAT	8925
rs758744080	snp	C/G	1.90856e-05	0.00308908	intron-variant	HERC1	GRCh38.p7	15:63716490	TTAAAGAAATTATCA[C/G]AAACTACACTAAATA	8925
rs758755867	snp	A/C/G	3.31308e-05	0.00406995	missense	HERC1	GRCh38.p7	15:63716371	GATGCCCCTCTTCCC[A/C/G]GTCTCTCTCAGCCTG	8925
rs758759952	snp	G/T	1.65605e-05	0.0028775	missense	HERC1	GRCh38.p7	15:63636022	CGCTGCCTGTCGCTG[G/T]TCCCATGGCCAAGTT	8925
rs758760739	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63757795	GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA	8925
rs758763575	snp	C/T	1.65745e-05	0.00287871	intron-variant	HERC1	GRCh38.p7	15:63638700	ATACAGTTATCTTCA[C/T]CTTTACTGACCTCAG	8925
rs758771535	snp	A/G	1.78899e-05	0.00299076	intron-variant	HERC1	GRCh38.p7	15:63652584	TAATTTTCTATTCAA[A/G]TGATTTTATTATTTG	8925
rs758771864	snp	A/G	3.39466e-05	0.00411973	intron-variant, missense	HERC1	GRCh38.p7	15:63658728	GGCAACCTGAAAAAC[A/G]TAATTCTGTTTTGTT	8925
rs758773894	snp	C/G/T	5.77499e-05	0.00537328	intron-variant	HERC1	GRCh38.p7	15:63774684	TAAAGTTGAGACTTA[C/G/T]AGTACGTACCAAAGA	8925
rs758777463	snp	G/T			missense	HERC1	GRCh38.p7	15:63694460	ACAATACGTTTAGCA[G/T]ACCAGTGGAAATTGC	8925
rs758780229	in-del	-/T	1.65627e-05	0.00287769	frameshift-variant	HERC1	GRCh38.p7	15:63636063	CCATCTCCCCAGCTA[-/T]AAGACCTCACCACTT	8925
rs758785574	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63700708	GCGAGACCCTGCCTC[-/A]AAAAAAAAAAAAAAA	8925
rs758802887	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63636653	TAATGGTGATGACAA[C/G]GAAAACGAGGATGAC	8925
rs758803570	snp	A/C	1.6615e-05	0.00288223	missense	HERC1	GRCh38.p7	15:63664542	CTGAGCGACCTCTAG[A/C]TGATGGTCCACTTCC	8925
rs758815284	snp	C/T	1.82941e-05	0.00302435	intron-variant	HERC1	GRCh38.p7	15:63626195	ATGAAGGAAACAGCA[C/T]TGCTTTCACTTTTCA	8925
rs758815891	snp	C/T			missense	HERC1	GRCh38.p7	15:63756673	CAAGGCCCAGTCTCC[C/T]ATAGCTGCCTTTCCC	8925
rs758847999	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63785368	CAAAGCTGTGAGCTA[A/T]AAGTGCACCACTGCA	8925
rs758850661	snp	A/T	0.000117094	0.0076507	intron-variant	HERC1	GRCh38.p7	15:63727641	TCTTTTATTGTCTTT[A/T]CTTACCATGAAGAGG	8925
rs758852867	snp	C/T	0.000356316	0.0133428	intron-variant	HERC1	GRCh38.p7	15:63747679	ACATGCACACACGCG[C/T]GCGCACACACACACA	8925
rs758861535	snp	A/T	1.67178e-05	0.00289113	synonymous-codon	HERC1	GRCh38.p7	15:63753045	AGCTTCAATAACTTT[A/T]GGTTTATACACTCTG	8925
rs758864094	snp	C/T	1.66322e-05	0.00288371	synonymous-codon	HERC1	GRCh38.p7	15:63675051	TCGCGCCACATCAAA[C/T]GGCAATGGTTCACAG	8925
rs758865517	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63664294	GCCTATGAATGTATG[A/C]TACGATTTAAATAAA	8925
rs758890506	snp	C/G/T			intron-variant	HERC1	GRCh38.p7	15:63785889	TCTTTTTCTTTTTTA[C/G/T]AGACAGAGGTCTCAC	8925
rs758900708	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63672276	CGACAGCTGATTAGA[C/T]CTGGGATCACCACTA	8925
rs758914735	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63794292	CTGAATTCTTTCTTG[A/C]GTGAGATCCAAGAAC	8925
rs758931929	snp	A/G	1.65921e-05	0.00288024	intron-variant	HERC1	GRCh38.p7	15:63694717	AACATAACTAGTACC[A/G]TAACCTCGGGCTAAA	8925
rs758935192	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63632946	TTCGACCCAAATCCA[A/C]ACCTGAAATGTTATT	8925
rs758938551	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63768712	GAAAAATGTTGAAAA[C/T]AGCATAAAGTTTTTA	8925
rs758939618	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63764224	CGGGACACAGCGTAG[A/G]AAGGGGAGAGACATA	8925
rs758940428	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63798650	CTACAATTATTTAGG[A/T]TTGTCACTCCCCTAA	8925
rs758955818	snp	C/T	1.7031e-05	0.00291808	intron-variant	HERC1	GRCh38.p7	15:63686570	GTCAGCATTTTGGAA[C/T]AATCCATGTCTCAGA	8925
rs758971797	snp	A/C	1.73057e-05	0.00294152	intron-variant	HERC1	GRCh38.p7	15:63665896	TAACACATGGAACAA[A/C]AGTACAGAAACTGGA	8925
rs758997381	snp	C/T	1.65905e-05	0.0028801	missense	HERC1	GRCh38.p7	15:63658646	ACACGGTCATGAGGG[C/T]TTGCTAGGGCAGCTG	8925
rs759008661	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63688176	GGCTTGGAATAGGGT[G/T]ATGACAGAAGAGATG	8925
rs759013265	snp	A/G	1.65597e-05	0.00287743	missense	HERC1	GRCh38.p7	15:63612447	TTCTTCAAGACTTCC[A/G]CAGAGATCTCGGGCA	8925
rs759016896	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63658499	CTTCCAGCTAATGTA[C/T]ACTAGAAGTTAACTT	8925
rs759017564	in-del	-/CTC	1.65696e-05	0.00287828	cds-indel	HERC1	GRCh38.p7	15:63756538	CCCAACTGAAGACTT[-/CTC]CTTCTGTCGTAAAGG	8925
rs759025554	snp	A/G	1.65982e-05	0.00288077	synonymous-codon	HERC1	GRCh38.p7	15:63727753	GAGGTAACTCAATAA[A/G]GGCCGAGCCACTGAC	8925
rs759038035	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63770879	CTAGTTCTCAGACAA[C/G]AGTAAAGTGTAAGAA	8925
rs759038993	snp	A/C	7.14886e-05	0.00597823	intron-variant	HERC1	GRCh38.p7	15:63623924	AAGCAATGAAATACA[A/C]CTCTTACCAATTTCC	8925
rs759043607	snp	A/G	1.65869e-05	0.00287979	synonymous-codon	HERC1	GRCh38.p7	15:63658633	CCTTAAAGCCACCAC[A/G]CGGTCATGAGGGTTT	8925
rs759055732	in-del	-/AG			intron-variant	HERC1	GRCh38.p7	15:63712459	AAAATAGGGAATAAA[-/AG]AGAAACAGGTTTGGA	8925
rs759062608	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63776631	TGAGATAATATTCTA[C/T]GTCTCAATACTGGTG	8925
rs759065325	snp	C/T			upstream-variant-2KB	HERC1	GRCh38.p7	15:63834726	CGCCTAACATAGGTC[C/T]AAGTGGACATTAAAT	8925
rs759073607	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63716663	TGTACACAAAATATA[C/T]AGACACATATATGCT	8925
rs759083301	snp	A/G	2.20437e-05	0.00331984	synonymous-codon	HERC1	GRCh38.p7	15:63641554	CATGTTCAATCCCAG[A/G]ACACCCTGCTGTTTC	8925
rs759085203	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63749956	TACAGCGATTTATCA[G/T]GCTGCCTTTAGGCAT	8925
rs759086324	snp	C/T	1.66247e-05	0.00288307	missense	HERC1	GRCh38.p7	15:63612345	CTCATGAAAAGCACC[C/T]GCTCCTCATTGGAGA	8925
rs759087630	snp	C/T	1.67787e-05	0.00289639	intron-variant	HERC1	GRCh38.p7	15:63725554	TGTCTTTATCTGGTA[C/T]TTTTAAGATTCAAAA	8925
rs759093745	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63628258	TTAGCCAGGAATGGT[A/G]GTGCATGCCTGTAGT	8925
rs759104746	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63671022	GCCTGACCAGCATGG[A/G]GAAACCCTGTCTCTA	8925
rs759108353	snp	A/C	1.6566e-05	0.00287797	intron-variant	HERC1	GRCh38.p7	15:63694763	TACATTTGCAGGAAC[A/C]GTTTACTTACCAATG	8925
rs759108486	snp	G/T	1.66327e-05	0.00288376	missense	HERC1	GRCh38.p7	15:63686516	AGATTCTCATCTTCT[G/T]CTTCCAACTCGCCCT	8925
rs759122041	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63681145	TCTGTTTAGAAAAAG[-/A]GTTAATATATTAAGC	8925
rs759122893	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63730279	GGGCAACACAGCAAG[A/C]CTTCACCTCTAAAAA	8925
rs759124846	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63715634	CAAAGGCATTGCTGA[C/T]CATGTTTTAGGGTAC	8925
rs759126793	snp	C/G	1.65864e-05	0.00287974	synonymous-codon	HERC1	GRCh38.p7	15:63623815	CCACGCTCGGGAAGG[C/G]AGGCGGAGGTCTGAA	8925
rs759136294	snp	C/T	1.65616e-05	0.00287759	missense	HERC1	GRCh38.p7	15:63636004	TCGATCTGCCTGGGC[C/T]GCCGCTGCCTGTCGC	8925
rs759136742	snp	A/G	3.28877e-05	0.00405497	intron-variant	HERC1	GRCh38.p7	15:63642918	TCTAAAGTTCCTTAC[A/G]AGCTTACACCCTATC	8925
rs759161898	in-del	-/CA	0.00024961	0.0111688	intron-variant	HERC1	GRCh38.p7	15:63747678	ACATGCACACACGCG[-/CA]CGCGCACACACACAC	8925
rs759164836	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63682060	CAGCAATGAGATTCA[A/C]TAGAACAACCCTGAT	8925
rs759168049	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63768524	CAAATTCCCTAGTTA[G/T]CTGTGAAGCATTTCT	8925
rs759176223	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63706193	TCATTAACAAAAGAC[C/T]TTAACTCTCAATGAC	8925
rs759215294	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63678954	CAGTTATTTTAAAGA[A/T]TAAATGAGATTATGC	8925
rs759216361	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63615507	CCCAGCTACTGGGGA[A/G]GCTGAGGCCAGAGAA	8925
rs759245584	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63729120	GGAATCTTCAATAGA[A/C]GGAAATTCAAGACCA	8925
rs759246829	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63614755	GACCACATGAGTGGT[C/T]ACTCATTCACACTCC	8925
rs759251241	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63827787	AGTATATTCACATAA[C/T]GGAATAACATTCAGT	8925
rs759256312	snp	C/G	1.87247e-05	0.00305974	intron-variant	HERC1	GRCh38.p7	15:63674306	AAATAATCTCAACAG[C/G]ACAAAAGCAAAAAAA	8925
rs759280991	snp	C/T	3.31603e-05	0.00407174	synonymous-codon	HERC1	GRCh38.p7	15:63664525	GTGTCTTCTTGTTAC[C/T]GCTGAGCGACCTCTA	8925
rs759283588	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63709744	GCACTGTGTAGGAGA[C/T]ATCAGGGGCATTTAG	8925
rs759293384	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63743923	CTGGGCTTATCTGTA[C/T]CCATCCTTCTTGGGC	8925
rs759301740	snp	A/G	1.75446e-05	0.00296176	synonymous-codon	HERC1	GRCh38.p7	15:63649759	CTCCAATTCTCGACG[A/G]TGCATGGTGGACACA	8925
rs759307643	snp	A/G/T	0.000132612	0.00814185	missense, synonymous-codon	HERC1	GRCh38.p7	15:63669545	ACACGCACCTGTGCG[A/G/T]TTAGCTGGCCTTGCT	8925
rs759311275	snp	C/T	1.66294e-05	0.00288347	missense	HERC1	GRCh38.p7	15:63674443	GCTAATCCCAATGCT[C/T]TCTTTATGGGTGACC	8925
rs759324456	snp	C/T	1.72347e-05	0.00293548	intron-variant	HERC1	GRCh38.p7	15:63626158	GTACTGACACACCTG[C/T]CCAGAAAGCAAATGG	8925
rs759325315	snp	A/C	4.89476e-05	0.00494686	intron-variant	HERC1	GRCh38.p7	15:63753129	ACTTGTTTTAAAGAA[A/C]CTCTACTCTTTTTAA	8925
rs759334615	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63722491	GGTTTCAGTTACTTG[C/T]GATCAACTGTGGTCC	8925
rs759335061	snp	C/T	1.71725e-05	0.00293018	missense	HERC1	GRCh38.p7	15:63645538	GGCGGCACCAAGCAA[C/T]GCCATTTACAATAGA	8925
rs759337262	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63694665	TATTTATTCTTTACC[C/T]ATAAGTTTATCTACT	8925
rs759341699	snp	A/G	1.65781e-05	0.00287902	missense	HERC1	GRCh38.p7	15:63754628	ATGTTGGAATGTTAC[A/G]ACTATTGCTGTCACC	8925
rs759358593	snp	C/T	1.70691e-05	0.00292134	synonymous-codon	HERC1	GRCh38.p7	15:63628678	ATTTCATTCCTCACC[C/T]GGTGCTCTTGGTGGG	8925
rs759370005	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63798872	AGCATTTAGTGGTTG[C/T]ATACTATTTCTTACT	8925
rs759378457	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63663994	TTATATTTTACATGC[A/C]CAGAACGTAATCCTA	8925
rs759385689	in-del	-/GAG			intron-variant	HERC1	GRCh38.p7	15:63609510	CTGTGTGTGTAAAGT[-/GAG]GAGAAGCTCTGACTG	8925
rs759411976	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63784578	CATAAATTTGAATTT[C/T]TTATATATGCATGTA	8925
rs759412132	snp	G/T	3.31873e-05	0.0040734	missense	HERC1	GRCh38.p7	15:63616528	CCTCCAGGTCCTCTA[G/T]GGTGAGTGGGACACA	8925
rs759427793	in-del	-/T	0.000134375	0.00819571	intron-variant	HERC1	GRCh38.p7	15:63643563	TCCTGAAATTCATTA[-/T]TTTTTAACATGCATT	8925
rs759444631	snp	C/T	4.41979e-05	0.00470075	missense	HERC1	GRCh38.p7	15:63694038	CCGTCTTCTTGCTCC[C/T]CTTCTCCGAAAGAGG	8925
rs759461833	snp	A/G	4.96824e-05	0.00498385	missense	HERC1	GRCh38.p7	15:63663126	TTAAAGTCATACAAC[A/G]CCCCTGGGTCTTGCT	8925
rs759463001	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63708759	TCAAAGATATGAACG[A/G]TAATCTTAAATAACC	8925
rs759466094	in-del	-/ATGAAAACACA			intron-variant	HERC1	GRCh38.p7	15:63725627	GCAAAATATTTTATG[-/ATGAAAACACA]AATTATAATACTTTC	8925
rs759468057	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63676195	GTGTGAGCCACCAAG[A/C]CCAGCCTACTGTATG	8925
rs759472880	snp	C/T	4.97929e-05	0.00498939	missense	HERC1	GRCh38.p7	15:63698951	CTGCTATGTTTCAGG[C/T]GAGCCCAAGAGTCAC	8925
rs759479133	snp	C/T	1.68493e-05	0.00290248	missense	HERC1	GRCh38.p7	15:63716458	CAACATCTGCAGAGT[C/T]CTGGTTTTCTGATAT	8925
rs759481146	in-del	-/A	0.000205656	0.0101383	intron-variant	HERC1	GRCh38.p7	15:63632612	CTCACCACCTAGAAC[-/A]AAAAAAAGGACTCAA	8925
rs759482009	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63631196	TCAACTTGTCTTGTC[C/T]TCAAACTTCCAACCA	8925
rs759503955	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63806659	TTAATTCTGGTCTAA[C/G]AAGTCTACGGAGAAA	8925
rs759508566	snp	A/G	1.67475e-05	0.00289369	missense	HERC1	GRCh38.p7	15:63633969	TTTAATCCACAGGCC[A/G]CCTAAAGAAATAACA	8925
rs759517354	in-del	-/ATA			intron-variant	HERC1	GRCh38.p7	15:63712978	AATTGGAGCACAGAG[-/ATA]ATATACACACACAGG	8925
rs759518169	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63632072	ACATTTCCACACATT[C/T]ATTTAGGGCAAATGG	8925
rs759532445	snp	A/G	4.97187e-05	0.00498567	synonymous-codon	HERC1	GRCh38.p7	15:63698833	ATTCCCCACATCTCC[A/G]CTCACAAAGCTTACA	8925
rs759550276	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63767931	TTCAGTCTCTTCATA[C/T]AGCTTCCTTTTCTCC	8925
rs759567034	snp	G/T	5.79727e-05	0.00538359	synonymous-codon	HERC1	GRCh38.p7	15:63718579	CAAACTTTACCCATC[G/T]GTCCCGTGATGATGA	8925
rs759569545	snp	A/G	3.31807e-05	0.00407299	synonymous-codon	HERC1	GRCh38.p7	15:63774772	GCTTGAGAGTAGTTT[A/G]CCTTTCTCCATGGTG	8925
rs759570400	in-del	-/AT			intron-variant	HERC1	GRCh38.p7	15:63829480	TATATGTTTATATAA[-/AT]ATATATATATATATA	8925
rs759590678	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63734470	CAAATAAACCACAGA[C/G]TGTCTGGCTTAGTAC	8925
rs759602040	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63687944	CAAGTTGCTTAGACT[A/G]TAGTGAGCAAAAGGG	8925
rs759604048	snp	A/G	3.31235e-05	0.00406948	missense	HERC1	GRCh38.p7	15:63680685	TAGAGCCACATATCC[A/G]AGGTAGTGCGGTGAT	8925
rs759624813	snp	A/G	1.68309e-05	0.00290089	missense	HERC1	GRCh38.p7	15:63616662	TGTTCATCGAGGCAG[A/G]CAGAAGGGTTAAAAA	8925
rs759636444	snp	C/T	4.48642e-05	0.00473604	synonymous-codon	HERC1	GRCh38.p7	15:63645632	GTCTTCTTTGGCACA[C/T]GTCATAAGAATATGA	8925
rs759638200	snp	C/T	1.67857e-05	0.00289699	missense	HERC1	GRCh38.p7	15:63656290	GCCAAGCACATTAAT[C/T]GAACTAGCGTTCGGA	8925
rs759639077	snp	A/T	1.66192e-05	0.00288259	missense	HERC1	GRCh38.p7	15:63725325	TTTCTACACCGTCAC[A/T]GAACAGTGGCGTTTT	8925
rs759639269	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63733430	CTGTAAGTAGAGAGG[A/G]GTACGAAATGCCAAT	8925
rs759649971	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63777330	GAGGGGGGAAAATCA[C/T]GATCCTCCATCCCAC	8925
rs759653725	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63819488	TCATTAGGTTTCAAG[A/G]TCTACCAAGAAAAGC	8925
rs759653892	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63699906	AGATACATAAATTTG[A/T]TTAACTACAATCCTT	8925
rs759655877	snp	A/T	0.000178958	0.00945764	intron-variant	HERC1	GRCh38.p7	15:63694168	AGGTCCTATGTGAAA[A/T]AAAAGAAAAAAATAA	8925
rs759661530	snp	C/T	1.66832e-05	0.00288814	missense	HERC1	GRCh38.p7	15:63651313	GATATTTGCCACTGA[C/T]ACTCCAGGAAACTGG	8925
rs759663822	snp	A/G	3.31351e-05	0.00407019	synonymous-codon	HERC1	GRCh38.p7	15:63669668	ACGTGTGGGAAGTAC[A/G]GTGGTAGTTGGGTAA	8925
rs759667353	snp	C/G	1.70122e-05	0.00291647	intron-variant	HERC1	GRCh38.p7	15:63749362	TTAAACATAGGCACT[C/G]TTACCTGTCCCTAGG	8925
rs759668113	snp	A/G			intron-variant, downstream-variant-500B	HERC1	GRCh38.p7	15:63669242	AGCATTTCAAAATGT[A/G]TGGGTTGCAGCTAAA	8925
rs759687236	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63780503	GAGGTGGGCGGATCA[A/C]GAGGTCAGGAGATTG	8925
rs759689082	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63788052	GAAAGAAAGTTCAAG[A/T]GCATTTAAAGAATAG	8925
rs759692189	snp	A/G	2.16823e-05	0.00329252	intron-variant	HERC1	GRCh38.p7	15:63634724	ATATCTTATTGATTT[A/G]TTCCATGCCTGTCCA	8925
rs759695135	in-del	-/GCATC	1.72704e-05	0.00293852	frameshift-variant	HERC1	GRCh38.p7	15:63675104	ATCACTAGGCGACCA[-/GCATC]AAAAGTTGGGAAGCT	8925
rs759695762	snp	C/T	3.4424e-05	0.00414859	synonymous-codon	HERC1	GRCh38.p7	15:63758337	ATCTGGGCTAGCACA[C/T]GTTCTCGAATAATCA	8925
rs759701658	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63714211	AAAGAAAAAAAAAAC[A/G]GACAAAATTTAAGTT	8925
rs759712855	snp	C/T	5.69947e-05	0.00533799	intron-variant	HERC1	GRCh38.p7	15:63680494	CGAGTTGACTATAAA[C/T]AGAAACAAGAAAAAT	8925
rs759712973	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63791925	ACTGTTCAAAAACAA[A/T]ATCACTGATTTAATC	8925
rs759720013	snp	A/G/T	3.31577e-05	0.00407161	synonymous-codon	HERC1	GRCh38.p7	15:63624259	AGTGTAGACTCTTGG[A/G/T]GCTAACAAAGGCCGA	8925
rs759739684	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63779596	ACTTTTCCACTAACA[G/T]GATCTATTTCTGGAT	8925
rs759762640	snp	A/G	6.85284e-05	0.00585316	synonymous-codon, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609147	GTAGTTGTCCATGTC[A/G]ATTGAGCGGCAGTTG	8925
rs759768454	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63746860	AATATATTGTATAGC[C/T]AAAATCTCAGAGAAA	8925
rs759779800	snp	A/G	0.000262594	0.0114555	intron-variant	HERC1	GRCh38.p7	15:63659954	GGAATTTAAATAAAT[A/G]AATGTATAGTATGTG	8925
rs759782772	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63624595	AGTTACTCAGGAGGC[G/T]GAGGTGGGTGGATCA	8925
rs759785785	snp	A/T	2.37138e-05	0.0034433	missense	HERC1	GRCh38.p7	15:63643513	TGTCCCCGCAGCTGA[A/T]AAACACACTTGGCTC	8925
rs759788433	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63711504	GAAGTATAAACAAAA[C/T]GTCATGATACAATGA	8925
rs759805106	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63832296	GTGTGTGTCTCTATA[A/C]ATATATACGTACATT	8925
rs759828467	snp	C/T	3.34253e-05	0.00408797	intron-variant, synonymous-codon	HERC1	GRCh38.p7	15:63654362	AGGATGGGCATACAA[C/T]TGGGCAATTAAACCT	8925
rs759837607	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63666935	CCTTTTCATAGTCTA[C/T]TTAGTGCTACATTCT	8925
rs759866978	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63623449	AAATGTACATATATG[C/T]CATTGTTATTCTGCC	8925
rs759867393	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63699032	CATATATCAATGGCA[A/G]TCAAGTAGAGCATAC	8925
rs759874959	snp	G/T	0.000200461	0.0100095	intron-variant	HERC1	GRCh38.p7	15:63637679	TAAATATTTTATTCT[G/T]TATTATATTGCTTTA	8925
rs759886260	in-del	-/A	3.42056e-05	0.00413541	intron-variant	HERC1	GRCh38.p7	15:63640109	CCCAATACCCATGAT[-/A]AAAATCTCAGCTGCA	8925
rs759889450	in-del	-/C	1.9025e-05	0.00308417	intron-variant	HERC1	GRCh38.p7	15:63664608	GCTACAAGTGCAAGT[-/C]GAGAAAGCAACACAA	8925
rs759891542	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63790700	CAACTTTGTGTGTTA[C/T]GTTTCCCTTTCTTTA	8925
rs759913014	snp	A/C/G	8.07337e-05	0.00635305	missense	HERC1	GRCh38.p7	15:63713627	CTCGGTCTCGGCTAC[A/C/G]AGCTACTTCACGGGC	8925
rs759913876	snp	C/T	1.65723e-05	0.00287852	synonymous-codon	HERC1	GRCh38.p7	15:63638474	TCTTCCAGCTTCTGC[C/T]AGCTGTCCATGCCTA	8925
rs759915381	snp	C/T	3.3157e-05	0.00407154	synonymous-codon	HERC1	GRCh38.p7	15:63749498	ATTTCCCTGACCACA[C/T]TGCCCCATTGAGTTA	8925
rs759927545	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63679445	GATAAAACCTGAAAG[C/T]TTCTACTACATAATG	8925
rs759937260	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63831229	CTCCCATCTCAGCCT[C/T]CCTAATAGCAGGAAT	8925
rs759940634	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63759991	GGGGCCAAGGGAGTC[A/C]GAATTGCTCATCTAC	8925
rs759954500	snp	A/G	1.65633e-05	0.00287774	missense	HERC1	GRCh38.p7	15:63718687	ATAAGTGTTTACCAG[A/G]TTGATATCTAAATGA	8925
rs759957200	snp	A/G	1.65737e-05	0.00287864	synonymous-codon	HERC1	GRCh38.p7	15:63660986	ACCTTCATACACACT[A/G]TCTTGCTTGCCAATT	8925
rs759966534	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63771094	CTGGGGAGGCTGAGG[A/C]ACGAGAATAGCTTGA	8925
rs759972144	snp	C/T	3.6543e-05	0.00427436	intron-variant	HERC1	GRCh38.p7	15:63615750	TTCATGTGTACCTCC[C/T]GAGATGTTTCATCTC	8925
rs759972515	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63649302	AGGTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC	8925
rs759974197	in-del	-/TT			intron-variant	HERC1	GRCh38.p7	15:63631573	GATGAAGTTTCGCTC[-/TT]TTGTCGCCCAGGCTG	8925
rs759975674	snp	C/G	1.65644e-05	0.00287783	missense	HERC1	GRCh38.p7	15:63775062	TGACATCGTTGCAAA[C/G]ACTGAGACCAGGTCC	8925
rs759992049	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63772491	TGTGACCATAAATAC[A/C]TTATTTTATTGTTTT	8925
rs760002810	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63712141	ATTTTGAGTAGAGGA[A/G]GTATAAACAGATTTG	8925
rs760004466	snp	C/T	1.65693e-05	0.00287826	missense	HERC1	GRCh38.p7	15:63729511	CCTCACTAATGTTAT[C/T]GATATGGCAAAATGC	8925
rs760008910	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63726375	CAATGAAATAAAAAT[-/A]AGAGACTGAAAAATC	8925
rs760018291	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63725191	CTGCTAATGTTGCAA[C/T]TGGTGCCTGTCAGTT	8925
rs760023312	snp	A/G	0.000110785	0.00744179	synonymous-codon	HERC1	GRCh38.p7	15:63615861	ACTATTTCCACCAGG[A/G]ATTATAGGAACCATT	8925
rs760023452	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63740061	GACTACAGGCATGCG[A/C]CACCAGACTCAACTA	8925
rs760027085	in-del	-/AGAC			intron-variant	HERC1	GRCh38.p7	15:63699770	TAAAATCTTTACATT[-/AGAC]AGACAGCAAAATGTT	8925
rs760027159	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63814927	ATGTGAGCTATGATT[A/G]TTACAAGTTCATGAA	8925
rs760031966	snp	A/G	3.69372e-05	0.00429735	intron-variant	HERC1	GRCh38.p7	15:63652364	ACCAAGATGAGGCAT[A/G]TTTAGGATTCTCTTA	8925
rs760039351	snp	C/T	6.65613e-05	0.00576855	missense	HERC1	GRCh38.p7	15:63690617	TGAAGTGCAAGGAGC[C/T]TTGTTCTTAAGTTAC	8925
rs760053774	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63725642	ATGAAAACACAAATT[A/G]TAATACTTTCTGTAT	8925
rs760059719	snp	C/T	1.71522e-05	0.00292845	intron-variant	HERC1	GRCh38.p7	15:63624349	CAGAAGGTACGGTTA[C/T]CAGAAATGGTACAAT	8925
rs760066601	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63660888	AAACACACACACACA[C/T]GAAGGTGAATTTTAG	8925
rs760070193	snp	C/T	3.018e-05	0.00388447	intron-variant	HERC1	GRCh38.p7	15:63696091	TTGTAAAATGACAGT[C/T]AAAATCTGTATATAC	8925
rs760074733	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63753421	CAAAATATACAGGTA[C/T]TATATGCGTATAATT	8925
rs760078639	snp	C/T	1.70206e-05	0.00291719	intron-variant	HERC1	GRCh38.p7	15:63727881	GACAATTGCTTCAAA[C/T]GAACTTTAAAAAAAG	8925
rs760081703	snp	C/T	1.65751e-05	0.00287876	missense	HERC1	GRCh38.p7	15:63665998	AATAACAGGGATCAT[C/T]TGACTTCCCGCCACT	8925
rs760083409	snp	C/T	1.65696e-05	0.00287828	synonymous-codon	HERC1	GRCh38.p7	15:63666044	TCCAGGCCTAGAGTC[C/T]GCTGTGCTGCCCGAC	8925
rs760092986	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63783195	GCTATCAAACAACAT[A/T]GCATGCTACAGAGAA	8925
rs760093477	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63690366	CACACCCCATAACTT[A/G]ATTTTTTTTGCCCTC	8925
rs760105167	snp	A/G	1.70551e-05	0.00292015	intron-variant	HERC1	GRCh38.p7	15:63754471	AAAACTCAAGAAAAA[A/G]GCCAAAGCTACTGAT	8925
rs760117528	snp	C/G	1.65748e-05	0.00287874	missense	HERC1	GRCh38.p7	15:63654226	GGTCGTGTGCAGCAA[C/G]AGTGCGCACGAGTTG	8925
rs760127140	snp	G/T	1.72326e-05	0.0029353	missense	HERC1	GRCh38.p7	15:63696197	AAACCAAAACACCCT[G/T]CTAGGAACTGCAGCC	8925
rs760135118	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63662362	ATTTTCATCTGGTCA[A/C]AAAATGCATACCTAC	8925
rs760149660	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63783839	TTGGGAGGCTGAAGC[A/G]GGCAGATCTCGAGGT	8925
rs760159671	snp	A/G	3.51512e-05	0.00419218	intron-variant	HERC1	GRCh38.p7	15:63643106	TTGAACTGTAGGTAT[A/G]ATTTACATTTAAATT	8925
rs760166699	snp	C/T	0.00042203	0.0145202	synonymous-codon	HERC1	GRCh38.p7	15:63718592	TCTGTCCCGTGATGA[C/T]GACCTTGTTTGAATA	8925
rs760181656	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63823912	AAATTATGTATCTGT[C/T]AATATCCAAAATGCG	8925
rs760191751	in-del	-/TTACC			intron-variant	HERC1	GRCh38.p7	15:63675824	AATCTTGGTTCTATA[-/TTACC]TTACCTTTCTATTTT	8925
rs760200693	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63738123	ATTAACCTCATGTAA[C/T]AACATACCAAGGACA	8925
rs760210069	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63705909	GTGGTGCACACCTGC[A/G]GTCCCAGCTACTTGG	8925
rs760234756	snp	A/T	9.33402e-05	0.00683091	intron-variant	HERC1	GRCh38.p7	15:63689745	TGTAAAAAGTAACTT[A/T]AAGTATTTTTAGAAA	8925
rs760240544	in-del	-/AC			intron-variant	HERC1	GRCh38.p7	15:63691446	ACTCCAGCCTGGGCG[-/AC]ACAGAGAGCCTCTGT	8925
rs760244075	snp	A/G	1.65839e-05	0.00287953	missense	HERC1	GRCh38.p7	15:63774782	AGTTTGCCTTTCTCC[A/G]TGGTGTGTACAACTG	8925
rs760246279	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63628387	AGAGCAAGACTCCAT[C/T]TCAAAAAAAAACTTA	8925
rs760253940	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63635898	GTTACCTAATTTTAA[A/G]AAACCTATTCAACAA	8925
rs760262485	snp	C/T	1.65622e-05	0.00287764	synonymous-codon	HERC1	GRCh38.p7	15:63774946	TCCTTTAAGAAATGT[C/T]GTTACTTGCGATAAG	8925
rs760269349	snp	A/G	1.65597e-05	0.00287743	synonymous-codon	HERC1	GRCh38.p7	15:63612458	TTCCACAGAGATCTC[A/G]GGCATCCCACACACC	8925
rs760271223	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63765440	TGATTCAGGCCAGGA[C/T]GGGAAGTGGGAGATC	8925
rs760281444	snp	C/T	1.72421e-05	0.00293611	intron-variant	HERC1	GRCh38.p7	15:63749352	ACAAGAATTTTTAAA[C/T]ATAGGCACTCTTACC	8925
rs760284175	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63659545	AGCATAAGCCACCAA[A/G]CCCAGCCAAAACTTA	8925
rs760288090	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63719661	TGATGACTCAGAAAA[A/T]GGTAAGAGCAGCGAA	8925
rs760288448	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63629875	TCATAGCATCTCAGA[C/T]ATCTCACACCAAGGT	8925
rs760296771	snp	C/T	1.67584e-05	0.00289464	missense	HERC1	GRCh38.p7	15:63628695	GTGCTCTTGGTGGGA[C/T]AGGTGGTGCTGTCCA	8925
rs760305236	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63795658	TAAATTTAATTTACT[C/T]AGCAAGGCCATTTTT	8925
rs760310860	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63744719	AGCTTATGGTGAATA[C/T]TGCCTGGCCTAGGTC	8925
rs760315246	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63673710	ATATCTCTGAGAAGA[C/T]ATCAGAATACTATGT	8925
rs760318914	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63718271	TTAAACAGGATAATT[C/T]AAATGTGGCCCAATC	8925
rs760322732	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63764308	TTTATATAATTATGT[A/G]CACTGAAACCAAATC	8925
rs760322735	snp	A/C	1.70145e-05	0.00291667	missense	HERC1	GRCh38.p7	15:63612553	CTTCTCGGACTGCAG[A/C]CACCTGCTCCCGGGA	8925
rs760355884	snp	A/G	3.31323e-05	0.00407002	synonymous-codon	HERC1	GRCh38.p7	15:63694787	ACCAATGTGATGCTT[A/G]TTTGCTTGCAGGGCT	8925
rs760401250	snp	G/T	1.73791e-05	0.00294775	intron-variant	HERC1	GRCh38.p7	15:63665889	AAATTTATAACACAT[G/T]GAACAAAAGTACAGA	8925
rs760427124	in-del	-/GGTA			intron-variant	HERC1	GRCh38.p7	15:63681565	CCTGGGAATTTGACT[-/GGTA]GGTAAAGTTTCTTAC	8925
rs760429038	snp	A/G	1.65636e-05	0.00287776	synonymous-codon	HERC1	GRCh38.p7	15:63640230	AAACTGGGCTCCATT[A/G]GTCAGGGCTTCGGCA	8925
rs760441820	snp	A/G	3.06415e-05	0.00391405	intron-variant	HERC1	GRCh38.p7	15:63642931	ACAAGCTTACACCCT[A/G]TCATTTGATATAACT	8925
rs760444823	snp	C/T	1.79903e-05	0.00299914	missense	HERC1	GRCh38.p7	15:63734740	TGTCCTTTAGATAAG[C/T]TTTCCCATCTATCAG	8925
rs760449040	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63816548	AAAGAACAAACATCA[A/G]TGACCAGCTCCATAC	8925
rs760449240	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63776693	CTAGTGGGCTGGGCA[C/T]GGTGGCTCACACCCA	8925
rs760450885	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63630405	TTATCTCTTTCCCCA[A/C]CTGAGGAACACTGTG	8925
rs760456325	snp	A/G/T	6.63013e-05	0.00575733	missense	HERC1	GRCh38.p7	15:63665992	ACTGCAAATAACAGG[A/G/T]ATCATTTGACTTCCC	8925
rs760458121	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63817679	AAGTTCGCGCCACTA[C/T]ACTCCAGTGTGGGTG	8925
rs760485127	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63804648	GAACACATACATAAA[G/T]AAGAAAATGAAAAGG	8925
rs760486609	snp	G/T	1.6601e-05	0.00288101	intron-variant	HERC1	GRCh38.p7	15:63733176	ATAGGAACAAGTAAC[G/T]AGCGTAATATGCACT	8925
rs760498095	snp	A/T	1.65677e-05	0.00287812	missense	HERC1	GRCh38.p7	15:63669556	TGCGGTTAGCTGGCC[A/T]TGCTGACTGGGAATC	8925
rs760516187	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63710705	CATTTTAAATAGGGT[A/G]GTCAGCACAGGCTTC	8925
rs760518970	snp	C/T	1.66015e-05	0.00288105	synonymous-codon	HERC1	GRCh38.p7	15:63725332	ACCGTCACTGAACAG[C/T]GGCGTTTTCATCCAA	8925
rs760544467	snp	C/G/T	3.38858e-05	0.00411606	intron-variant	HERC1	GRCh38.p7	15:63616686	TTAAAAAGGAACCTG[C/G/T]AAAATTAAAGGGAAT	8925
rs760563299	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63785111	ATATATAAAGACTCA[A/T]ATGCTCCATTTCTAA	8925
rs760564287	snp	C/T	1.71823e-05	0.00293101	missense, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609163	ATTGAGCGGCAGTTG[C/T]TGATGGCATAGCGCA	8925
rs760574108	snp	C/T	1.66128e-05	0.00288204	missense	HERC1	GRCh38.p7	15:63677876	CTTCATCCCATTGGA[C/T]CTTGGCAGACGTGCT	8925
rs760590340	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63651958	GCAGAATCACTTGAA[C/T]CCAGGAGGCAGAGGT	8925
rs760599226	snp	A/G	3.23525e-05	0.00402184	missense	HERC1	GRCh38.p7	15:63718665	TATACACAACGGTAC[A/G]CTTCTGATAAGTGTT	8925
rs760607346	snp	A/G	1.66205e-05	0.00288271	intron-variant	HERC1	GRCh38.p7	15:63754661	GACCTTGGATAAAAC[A/G]CACACAACAACAAAG	8925
rs760607774	snp	C/T	1.69183e-05	0.00290841	missense	HERC1	GRCh38.p7	15:63694369	ACTTTCAAAGCTGTG[C/T]TAAGCTGGGAAACAC	8925
rs760634440	snp	A/T	1.67719e-05	0.0028958	intron-variant	HERC1	GRCh38.p7	15:63628826	CCGAGCTGGGAATAA[A/T]TCACAAATATACAGA	8925
rs760636290	snp	A/C	1.66123e-05	0.00288199	synonymous-codon	HERC1	GRCh38.p7	15:63616547	GAGTGGGACACAGCA[A/C]AGCTGCTTCCACACC	8925
rs760639805	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63695857	ACTCCAATCCCTATC[C/T]TTACTTGGATCTATT	8925
rs760642659	snp	A/C	1.66407e-05	0.00288446	missense	HERC1	GRCh38.p7	15:63698966	CGAGCCCAAGAGTCA[A/C]TCAGGGATTCCAATT	8925
rs760665862	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63821554	GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	8925
rs760685095	snp	A/G	3.33139e-05	0.00408116	intron-variant	HERC1	GRCh38.p7	15:63669721	AAAATAACAGTGGTT[A/G]GCATAAAAATCCAAT	8925
rs760693925	in-del	-/AA			intron-variant	HERC1	GRCh38.p7	15:63818741	GAAATGGGACATACT[-/AA]ACTTTTATCAACATT	8925
rs760696274	snp	A/C	0.00108373	0.0232528	intron-variant	HERC1	GRCh38.p7	15:63694272	AAATGGAGGAAGACC[A/C]GACTTCATACAGTTC	8925
rs760696348	snp	C/T	1.90054e-05	0.00308259	intron-variant	HERC1	GRCh38.p7	15:63706769	ACTATGTTCTTAATA[C/T]TTACACTTACCTCTC	8925
rs760705965	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63709774	GGAAAAATAAAAACC[A/C]AAAAATCCTAGATTT	8925
rs760716930	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63768232	TTTTAATTATTTAGG[A/G]TGTTGCTTCTCAAAT	8925
rs760720907	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63727851	CATCTATGAAGGGCA[A/G]GAAATTAAACATGGG	8925
rs760737114	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63799046	AGATACGTTTCAGAA[A/C]TAGGTCATACTTGCA	8925
rs760745264	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63677300	TTAAATACCCAGTTT[A/G]TGTTAAATAAATGTA	8925
rs760763668	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63827866	TGACAAAATTATGCT[A/G]AGTGAAAGAAGCCAG	8925
rs760768173	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63722853	GGTACGGTACTACCT[C/G]TGGTTTCAAGCAATC	8925
rs760778652	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63687963	TGAGCAAAAGGGAAA[A/G]GTCAAGGAACTCTAG	8925
rs760778841	snp	C/T	1.65614e-05	0.00287757	synonymous-codon	HERC1	GRCh38.p7	15:63680714	ATTAAAGTCATGTAC[C/T]GGCCAGCGAGAAACT	8925
rs760789630	snp	C/T	1.84221e-05	0.00303492	intron-variant	HERC1	GRCh38.p7	15:63652377	ATGTTTAGGATTCTC[C/T]TATTTTAAATGGTAT	8925
rs760789761	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63633782	TATTTCCAACTAATA[A/G]TAACTACTGACATAG	8925
rs760795318	snp	A/C	1.65619e-05	0.00287762	missense	HERC1	GRCh38.p7	15:63663145	CTGGGTCTTGCTGCA[A/C]AGATATTCCTTCTCT	8925
rs760797030	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63747697	GCACACACACACACA[A/C]AGATACAAAACATAC	8925
rs760800432	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63769348	CTGCTTGAACCTGGG[A/T]GGCGGGAGCTGCAGT	8925
rs760815149	in-del	-/A			intron-variant	HERC1	GRCh38.p7	15:63798547	ATCTTCAAACTTTAC[-/A]AAAAAAAAAAAAAAA	8925
rs760819202	snp	A/C/T	6.62497e-05	0.00575509	synonymous-codon	HERC1	GRCh38.p7	15:63725437	AGCAATTGTTCTTTC[A/C/T]AGATCCACAAGCCAT	8925
rs760820700	snp	C/T	2.89868e-05	0.00380691	missense	HERC1	GRCh38.p7	15:63643541	CTCCTGATGATTTCC[C/T]ATATCCATCCTGAAA	8925
rs760821490	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63721457	TTTGAACTCGGAAGG[C/T]GGAGGTTGCAGTGAG	8925
rs760829940	snp	C/T	1.65963e-05	0.0028806	missense	HERC1	GRCh38.p7	15:63674777	CCACACTTGGCAGTG[C/T]TGGATCTAAAGAAAA	8925
rs760834835	snp	A/C	8.89363e-05	0.00666785	intron-variant	HERC1	GRCh38.p7	15:63749579	ATAAAAGAAAAGCCA[A/C]ATTCAAATGTAATAT	8925
rs760848834	snp	A/C	6.48824e-05	0.00569535	intron-variant	HERC1	GRCh38.p7	15:63749797	AAGCATAGACCTGAA[A/C]AAAACAGAAATACGT	8925
rs760851641	snp	A/G	2.04284e-05	0.0031959	missense	HERC1	GRCh38.p7	15:63626049	TCAGAGAAGTGGTAG[A/G]GCAGCCGGAGCCTGG	8925
rs760854779	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63691163	GAGTAAACAGACTAT[A/C]CTTTTCTAAAGTAAG	8925
rs760868686	snp	C/T			missense	HERC1	GRCh38.p7	15:63749470	TCTTTGGTTTAGTAA[C/T]AGGACCTGTGGAATT	8925
rs760873384	snp	C/G	1.79474e-05	0.00299556	intron-variant	HERC1	GRCh38.p7	15:63615765	CGAGATGTTTCATCT[C/G]ACCTGTCTGTCCATC	8925
rs760878985	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63617498	CCTTATAGCAGAATG[C/T]TTTATAATCCTTTGG	8925
rs760879871	snp	C/G	1.74613e-05	0.00295472	missense	HERC1	GRCh38.p7	15:63696218	AACTGCAGCCTCACA[C/G]ACGTGAGTAGTGTGG	8925
rs760897493	snp	C/G			upstream-variant-2KB	HERC1	GRCh38.p7	15:63834310	CATGCAGTGCGCCCC[C/G]TTTTCCTCGTGGTGG	8925
rs760902242	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63632307	TACTCAAGATTTGAA[A/C]CCAGAGTGCCTATGA	8925
rs760903018	snp	A/G	4.34896e-05	0.00466293	missense	HERC1	GRCh38.p7	15:63713639	TACGAGCTACTTCAC[A/G]GGCTGAGAGGAAACA	8925
rs760921271	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63609554	TGAGAGAATACACTA[C/T]GCACAGCGCCTGGCA	8925
rs760923920	snp	C/T	3.31691e-05	0.00407228	intron-variant	HERC1	GRCh38.p7	15:63638670	TTAGAATCAAAACAT[C/T]GACTGAGAACCATCA	8925
rs760925920	snp	C/T	3.43036e-05	0.00414133	intron-variant	HERC1	GRCh38.p7	15:63718919	ATAAAAATGATGCAT[C/T]GACATTTAAAAGGGC	8925
rs760928689	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63689074	GAAGGCAAGGTAAAA[C/G]TGGCACCAAAAAAGA	8925
rs760935609	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63629919	ATAAATAGAGGAGGG[C/T]GAATACATCAACCTC	8925
rs760946536	in-del	-/CTTCA	4.68307e-05	0.00483872	intron-variant	HERC1	GRCh38.p7	15:63696368	ACATATTTTAGAGTT[-/CTTCA]CTTAACTCAGACATG	8925
rs760948152	snp	C/G			missense	HERC1	GRCh38.p7	15:63734773	CCTTGAGGTAAAAGA[C/G]AATGAAGTAATTCCA	8925
rs760964831	snp	A/G	1.66421e-05	0.00288458	intron-variant	HERC1	GRCh38.p7	15:63648249	TAATTATTTGTCATT[A/G]TCTGACTTAAAAGAC	8925
rs760985908	snp	C/T	5.05242e-05	0.00502589	synonymous-codon	HERC1	GRCh38.p7	15:63712826	CAAATCAGATTCACT[C/T]CTCGATTTGATCAGT	8925
rs761001154	snp	A/G	1.65737e-05	0.00287864	synonymous-codon	HERC1	GRCh38.p7	15:63630499	CCCCCAGGCATACAC[A/G]TCTCCATTTGATGCC	8925
rs761009479	snp	A/G			downstream-variant-500B, intron-variant	HERC1, FBXL22	GRCh38.p7	15:63608145	ACCTTCCACTTGGCT[A/G]CCCTCCCCACTGAGA	8925
rs761019047	in-del	-/TGAG			intron-variant	HERC1	GRCh38.p7	15:63658389	AACTGAATGACCGAT[-/TGAG]TGAATAACAATGACT	8925
rs761020990	snp	C/T	1.66699e-05	0.00288698	missense	HERC1	GRCh38.p7	15:63651337	AAACTGGTGAGAAAC[C/T]TGGATCACTGGGTGA	8925
rs761037515	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63701709	ACAGGAAACACACTA[C/T]GTGGAAGCATCAGGA	8925
rs761040273	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63779670	ATTACAATAGGCTTA[C/T]AAATGTATAAATGTT	8925
rs761061047	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63657016	GTCTTTAGGGGGCAC[A/C]TATTTAAGTATTTCT	8925
rs761063908	snp	C/T	1.66167e-05	0.00288237	missense	HERC1	GRCh38.p7	15:63678188	TACATATCTTAATTT[C/T]GTGAAGCCTTTCCAT	8925
rs761069936	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63820673	AAAATCAAAAGCAAC[A/T]GAGACGTTATCCTTT	8925
rs761076946	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63669785	TAGAAGAATATGCAA[C/T]CTGGAAGACTAAACA	8925
rs761082158	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63668223	AAAGGCATACACACC[C/T]CAATTAAAAGGTAGA	8925
rs761088205	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63760133	AATTGAACTGGATAG[A/G]GACAACAGAAAGGAA	8925
rs761090999	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63792020	TGATAACTGATTTAA[C/T]TTTTCATTTTTCCAA	8925
rs761118420	snp	A/T	1.65677e-05	0.00287812	intron-variant	HERC1	GRCh38.p7	15:63656005	TACATGTAATTTTGG[A/T]ACAAAAATATTTCAT	8925
rs761125540	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63700485	ATTTTTGAATTACTA[C/T]ACTGGTGTCAATTAA	8925
rs761144065	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63802513	TCACAATCCTGATCA[A/G]CCAGCTAAATATTGG	8925
rs761150095	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63714854	ACCTGGCCCAAAGAC[A/G]GTATTCTTAATGGGA	8925
rs761150859	in-del	-/CTTCATGAACAAC	1.73933e-05	0.00294895	frameshift-variant	HERC1	GRCh38.p7	15:63675110	AGGCGACCAAAAAGT[-/CTTCATGAACAAC]TGGGAAGCTTTAATA	8925
rs761151398	snp	G/T	1.65627e-05	0.00287769	missense	HERC1	GRCh38.p7	15:63645000	ATGTTACCTGGCAAT[G/T]TGATTCCTGCTCCCA	8925
rs761162158	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63794710	CTCTAGCAGGAGATG[C/T]CACTCTTTCATCTTA	8925
rs761166192	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63768903	AGATCTCAAAACTGA[G/T]AGCAATAATTATTAT	8925
rs761166996	snp	A/C/T	8.06322e-05	0.00634898	missense	HERC1	GRCh38.p7	15:63723223	CTGATCCAAAGGCTT[A/C/T]GGGCAGGCTCTTTAG	8925
rs761170664	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63681564	GACCTGGGAATTTGA[A/C]TGGTAAAGTTTCTTA	8925
rs761172105	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63692851	AGAACAGAACAGTCT[A/C]GGAAGAAGTCGAGCT	8925
rs761204358	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63741293	CAGCCTCTCAAAGTG[A/C]TGGGATTACAGGCGT	8925
rs761205207	snp	G/T			missense	HERC1	GRCh38.p7	15:63713494	ATCACGGAGTTGCAT[G/T]CAGCAGTGTACACAT	8925
rs761218717	in-del	-/TTC	0.000181923	0.00953564	intron-variant	HERC1	GRCh38.p7	15:63678409	ACATGCTATTAGTAG[-/TTC]TTCTTAGTCACTATA	8925
rs761220132	snp	C/T	1.65729e-05	0.00287857	missense	HERC1	GRCh38.p7	15:63661018	GATCTGGAGCTTGTC[C/T]CTTGTACCTGCACCA	8925
rs761222484	snp	A/C	3.33561e-05	0.00408374	missense	HERC1	GRCh38.p7	15:63690647	CCAACCAGAGGGATA[A/C]CTGGAGGGGAAAAGA	8925
rs761233146	snp	A/G	8.91703e-05	0.00667661	intron-variant	HERC1	GRCh38.p7	15:63648038	TTATATTTGTATCCC[A/G]TAAAATTACGTTTTT	8925
rs761235368	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63826196	CCTAAATTTCCAGTG[C/T]TGCTGGGCAGCACTT	8925
rs761249099	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63815283	TTCCATATCTTGCAA[C/T]ATAGAGTAGTGACTA	8925
rs761264488	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63773834	ACAGGCATGAGACAC[C/T]GCACCCAGCCTAAAT	8925
rs761265783	snp	C/T	0.00562463	0.0527321	synonymous-codon	HERC1	GRCh38.p7	15:63706823	CAAATCAACATTTCG[C/T]CTGCCACTCTATTAA	8925
rs761270211	snp	C/T	3.37501e-05	0.00410779	intron-variant	HERC1	GRCh38.p7	15:63630463	AGCAATATAAATATT[C/T]ACCTGCCCTTCTGAA	8925
rs761293652	snp	A/G	2.96705e-05	0.00385154	synonymous-codon	HERC1	GRCh38.p7	15:63718676	GTACACTTCTGATAA[A/G]TGTTTACCAGGTTGA	8925
rs761310341	snp	C/T	1.6574e-05	0.00287867	missense	HERC1	GRCh38.p7	15:63638488	CCAGCTGTCCATGCC[C/T]ACCAGCACCCCATAA	8925
rs761346378	in-del	-/ATTCTATAGC			intron-variant	HERC1	GRCh38.p7	15:63735079	AAATATTTAGTGTTG[-/ATTCTATAGC]ATTCACCCTGGTAAG	8925
rs761354625	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63786671	TATATAATGTATGAT[C/T]CTATTTATAAGAAAT	8925
rs761356311	snp	C/T	6.08384e-05	0.00551502	intron-variant, missense	HERC1	GRCh38.p7	15:63654357	TAGGAAGGATGGGCA[C/T]ACAATTGGGCAATTA	8925
rs761357549	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63633786	TCCAACTAATAATAA[C/G]TACTGACATAGATGA	8925
rs761365611	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63725846	TTTAGGGAGTATTCT[A/G]AGTTTATTCCTCCAA	8925
rs761390841	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63772678	AAAACACAAAGAGGC[C/T]TACACGCCTCCCACA	8925
rs761392521	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63715474	ACTCCCTTTACTCCA[-/T]TTGGATCTTTTTCCT	8925
rs761400639	snp	A/G	1.66413e-05	0.0028845	synonymous-codon	HERC1	GRCh38.p7	15:63690610	AAGGACATGAAGTGC[A/G]AGGAGCCTTGTTCTT	8925
rs761404083	snp	C/T	4.96956e-05	0.00498451	missense	HERC1	GRCh38.p7	15:63775053	CAGTATGAATGACAT[C/T]GTTGCAAAGACTGAG	8925
rs761409118	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63636514	GACCTCAAGTGATCC[A/G]CCCACCTCGGCCTCC	8925
rs761411375	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63754801	AATCATTTCTAACAT[A/C]TTCTCAATCTTCCAA	8925
rs761444799	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63783884	CATCCTGGCCAACAT[A/G]GTGAAACCCCGTCTC	8925
rs761445702	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63795808	TGGCTGGAACGGGAC[C/T]TGACATTCTGTATTT	8925
rs761449867	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63673790	AGTGCAGTGGCACAA[C/T]CTCGGCTCACTGTAA	8925
rs761451003	snp	C/T	0.000273659	0.0116942	intron-variant	HERC1	GRCh38.p7	15:63616706	TTAAAGGGAATATTT[C/T]AAACAGCATTTTCCT	8925
rs761458741	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63630873	AAAATTTTTTAAAAA[A/G]TTGTATCTAAACTCG	8925
rs761472743	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63753808	CTGGTTTTATAAATT[G/T]TGCCACCATCAAATA	8925
rs761489358	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63748772	TAAAATACATTCTAA[C/G]CTATAAATTAGCCCA	8925
rs761490073	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63740250	GGTTAGGTTGTAGTA[C/T]GTATCACTACTTCAC	8925
rs761490358	snp	C/T	0.000101082	0.00710849	missense	HERC1	GRCh38.p7	15:63718600	GTGATGATGACCTTG[C/T]TTGAATAAGTTCAAG	8925
rs761500447	snp	A/T	1.84664e-05	0.00303856	intron-variant	HERC1	GRCh38.p7	15:63690516	AATATGGAAAACATC[A/T]TCTAATAATTTTAAA	8925
rs761502307	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63825114	GGGAGTTCGAGAGCA[C/G]TCTGGCCAACTTGGC	8925
rs761508786	snp	A/G	4.97071e-05	0.00498509	synonymous-codon	HERC1	GRCh38.p7	15:63666038	GGCTGCTCCAGGCCT[A/G]GAGTCTGCTGTGCTG	8925
rs761512488	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63707335	GGTAGTATTTGAAAA[C/G]ATTTTTAAATGTCTT	8925
rs761525337	snp	A/G	1.66696e-05	0.00288696	missense	HERC1	GRCh38.p7	15:63658565	GAGAGAAGAGACAGC[A/G]CTCTCATGACCATGG	8925
rs761531390	in-del	-/AT			intron-variant	HERC1	GRCh38.p7	15:63811139	AAGCAACTATAAAAG[-/AT]ATGTGGGAAACAAGA	8925
rs761544576	snp	A/C			missense	HERC1	GRCh38.p7	15:63661012	CAATTAGATCTGGAG[A/C]TTGTCCCTTGTACCT	8925
rs761545641	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63796721	GGCTGGACAACTTGA[A/G]GCAGAAGCTTTCAGG	8925
rs761553029	snp	A/T	1.67075e-05	0.00289023	intron-variant	HERC1	GRCh38.p7	15:63664451	TTCACAAAGAAAAGG[A/T]TACGGAACATAAAAT	8925
rs761574424	snp	A/G	3.32884e-05	0.00407959	intron-variant	HERC1	GRCh38.p7	15:63725528	CCTAAAGACAAAATC[A/G]TTAGTTATTGTGTCT	8925
rs761575424	snp	A/G	1.84391e-05	0.00303632	synonymous-codon	HERC1	GRCh38.p7	15:63634760	ATATCCCTCCAGTGC[A/G]GTCACTCTCTCTGGA	8925
rs761583916	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63650711	CTGATAACCAAATTG[C/G]CATAAGAAACTTACT	8925
rs761587795	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63765573	CTTCATCTGCATGAT[A/T]AAACCTACCTCTCCC	8925
rs761592911	in-del	-/C			intron-variant	HERC1	GRCh38.p7	15:63744608	CCAAAGCTAGAGGAG[-/C]CTCGCCCCATAGCTA	8925
rs761597330	snp	C/T	1.65767e-05	0.00287891	synonymous-codon	HERC1	GRCh38.p7	15:63654233	TGCAGCAAGAGTGCG[C/T]ACGAGTTGCTGAGCT	8925
rs761597536	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63719573	TTGAAAGCTCACTCT[A/G]CTGAGTGGAGAACTG	8925
rs761605569	snp	A/G	1.65625e-05	0.00287766	synonymous-codon	HERC1	GRCh38.p7	15:63774960	TTGTTACTTGCGATA[A/G]GCAGTCCAAGCCCAT	8925
rs761614665	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63806873	CTGCCTCAGCCTCCC[A/G]AACAGCTGGGATTAC	8925
rs761628465	snp	A/G	1.79053e-05	0.00299204	intron-variant	HERC1	GRCh38.p7	15:63634898	AGACATCTAAGACAG[A/G]ACCAAGGAGAAAGAA	8925
rs761631167	snp	C/T	3.56805e-05	0.00422362	intron-variant	HERC1	GRCh38.p7	15:63658501	TCCAGCTAATGTACA[C/T]TAGAAGTTAACTTAG	8925
rs761637230	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63714414	ATCACCAGGAATACC[C/T]ATCTGATGCCAGCCT	8925
rs761640811	snp	A/C	2.43929e-05	0.00349226	missense	HERC1	GRCh38.p7	15:63713659	GAGAGGAAACACTGA[A/C]AGATTTCTGTAACAT	8925
rs761642890	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63764471	CAGGGCTCTCGAAAC[A/C]ATCAAGGAAGTGGAA	8925
rs761643375	snp	A/C/T	0.00172239	0.029297	missense	HERC1	GRCh38.p7	15:63725441	ATTGTTCTTTCTAGA[A/C/T]CCACAAGCCATACCC	8925
rs761647783	snp	A/G	7.68182e-05	0.00619703	intron-variant	HERC1	GRCh38.p7	15:63640469	AAATACAAGGATATA[A/G]TATGTCAAAGAGTTT	8925
rs761664661	in-del	-/TCTG			upstream-variant-2KB	HERC1	GRCh38.p7	15:63835491	TCACAAATATGATAT[-/TCTG]TCTTTCTTGAATTTG	8925
rs761671199	snp	A/T	2.0578e-05	0.00320758	missense	HERC1	GRCh38.p7	15:63746931	ACCTCTTGGATTTCA[A/T]CTGGGACAGTTGAGT	8925
rs761674054	snp	A/G			missense	HERC1	GRCh38.p7	15:63677860	CTGATAGTAATTTCT[A/G]CTTCATCCCATTGGA	8925
rs761682429	snp	C/T	1.83717e-05	0.00303076	intron-variant	HERC1	GRCh38.p7	15:63652394	ATTTTAAATGGTATA[C/T]ACGTGATGTTAGCAC	8925
rs761710568	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63698622	GTACAGGAAAGGGGA[A/G]GGCAAGGAATAGAAG	8925
rs761717326	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63800165	AGAAAGAAACTGGGG[C/T]ATGGGGAAATATTCT	8925
rs761725682	snp	G/T	1.65712e-05	0.00287843	missense	HERC1	GRCh38.p7	15:63640361	GGTTACACAACAGCT[G/T]ATCCAGATGAAGTCC	8925
rs761732040	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63653148	AAGTAATTTTAAAAA[C/T]TGTTTAAGTAGGCCA	8925
rs761736129	snp	G/T	1.65795e-05	0.00287914	intron-variant	HERC1	GRCh38.p7	15:63661042	TGCACCAAACATGAA[G/T]AACATTGCATTTTTA	8925
rs761738977	snp	C/T	2.28867e-05	0.00338272	missense	HERC1	GRCh38.p7	15:63672575	CTGGAGTGGTGGCAG[C/T]TGTGGTGTCCTCCAG	8925
rs761739102	snp	C/T	6.63086e-05	0.0057576	missense	HERC1	GRCh38.p7	15:63663033	ATTCCCAGAATATCA[C/T]TGTCACTGGTCAGGT	8925
rs761748895	snp	C/T	3.25653e-05	0.00403505	intron-variant	HERC1	GRCh38.p7	15:63612242	AGGAAAAAAGAATAG[C/T]TTACTTACCCTATCA	8925
rs761757990	snp	C/T	3.36474e-05	0.00410153	synonymous-codon	HERC1	GRCh38.p7	15:63712778	GGGTATACCTACCAG[C/T]GCGTAACCCTCTTCA	8925
rs761763593	in-del	-/AAC			intron-variant	HERC1	GRCh38.p7	15:63764270	TAAACAGTCTACAAA[-/AAC]AACACCTATTTGAAG	8925
rs761767970	snp	A/T	1.76232e-05	0.00296838	missense	HERC1	GRCh38.p7	15:63734789	AATGAAGTAATTCCA[A/T]CCGTTCTCGTAATGG	8925
rs761773150	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63732029	TGTTTTGAGATGGGG[A/T]CTCGCTCTGTCACCC	8925
rs761782748	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63684708	CTACCTTCTAGCGGG[A/G]GAAAAAAATCTATGT	8925
rs761793616	snp	A/G	2.87377e-05	0.00379052	missense	HERC1	GRCh38.p7	15:63622875	ATAAGAAGGTCAACA[A/G]TACCAGTTTCAAGTT	8925
rs761796583	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63654028	AGAGTGACACAAAGA[C/G]AGAGACCTAAACTTT	8925
rs761797214	snp	C/G/T	6.5145e-05	0.00570693	intron-variant	HERC1	GRCh38.p7	15:63615924	AAGAGGAATCATCTA[C/G/T]GAACAGAAGAAAACA	8925
rs761798576	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63697643	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCACGC	8925
rs761810927	snp	C/T	3.32651e-05	0.00407817	missense	HERC1	GRCh38.p7	15:63694490	CCAAAGAAACATCTA[C/T]TGGTTGATAATGAAC	8925
rs761819885	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63665330	CGAAGTCTGGAGTTC[A/G]AGACCGTCCTGGCCA	8925
rs761840583	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63823058	TTGTTATATAAGTAA[A/G]CTCATGTCATGGGGG	8925
rs761843177	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63829775	ATAAGATGAGCATGG[A/C]ACAGCCTGTGGCCCC	8925
rs761846635	snp	A/G	8.39666e-05	0.00647891	intron-variant, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609283	TGTGGAGAGAGACCC[A/G]GAGCCGTGACTGGGG	8925
rs761846742	snp	A/G	1.65614e-05	0.00287757	synonymous-codon	HERC1	GRCh38.p7	15:63680735	GCGAGAAACTCCAAC[A/G]CACGTGCCTTCATTA	8925
rs761866702	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63730972	GACTGCTACTATAAT[A/T]TTTTTTGGTGTATTT	8925
rs761868937	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63635549	CTATACAATCTTACA[A/C]TATGATTTTAGAACA	8925
rs761877909	snp	A/G	3.39922e-05	0.00412249	synonymous-codon	HERC1	GRCh38.p7	15:63626120	CTGGGGGGGCACTGT[A/G]TCAGGCAGGCCCAGC	8925
rs761884471	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63666586	TAATGAAATTTTCCT[C/T]TACTCAGAATATGTG	8925
rs761894705	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63788298	GCATTTCAAAAAAAC[C/T]AATTTAACAGTTATT	8925
rs761895486	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63693908	CTAATCATATGCACA[C/G]AATGGGGTTTTAATA	8925
rs761897242	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63757634	CTATTCTTAACACTT[C/T]TTAAAAATCGAGATC	8925
rs761908954	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63710864	AACAGCTAAGAGTCC[A/T]GTGTGACAGAAGGAG	8925
rs761921480	snp	C/T	3.31592e-05	0.00407167	synonymous-codon	HERC1	GRCh38.p7	15:63752961	CCTTAGTCCTACCTG[C/T]CCTGTTGATGTCAAA	8925
rs761923729	in-del	-/AA			intron-variant	HERC1	GRCh38.p7	15:63730028	TGAAACTATGTCTCA[-/AA]AAAAAAAAAAAAAAA	8925
rs761925592	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63758983	ATCCTCCCACCTCAG[C/T]CCCCCAAGTAGCTGA	8925
rs761933558	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63733421	ATTTTAGTACTGTAA[A/G]TAGAGAGGAGTACGA	8925
rs761942463	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63769552	TCCAAAAATAAAGTC[A/G]AAATTAAAATAAATT	8925
rs761949130	snp	A/T	1.65688e-05	0.00287821	synonymous-codon	HERC1	GRCh38.p7	15:63729569	CAGTTCATGAAGATG[A/T]GCAGGCTGACTGTTT	8925
rs761949248	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63744427	CCGTGTCCTTCCCTT[C/T]AGGGGGAGTGAGGTC	8925
rs761953292	snp	A/C	3.3123e-05	0.00406945	missense	HERC1	GRCh38.p7	15:63645007	CTGGCAATTTGATTC[A/C]TGCTCCCACCATCCT	8925
rs761964002	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63709822	AAGACATACTAATAA[C/T]ACATAAATAAGTCCA	8925
rs761966849	snp	C/T	3.34666e-05	0.0040905	intron-variant	HERC1	GRCh38.p7	15:63666318	TAAGCTAGGACTTCT[C/T]ATATCTGTATACACT	8925
rs761976318	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63770655	GGGCAGCAGAGATTA[A/G]GAATCACACAAGTAA	8925
rs761981975	in-del	-/G	3.16261e-05	0.00397643	frameshift-variant	HERC1	GRCh38.p7	15:63648190	AACCATGCAATGCAA[-/G]TAACAGACACTAACA	8925
rs761988716	snp	C/T	3.31763e-05	0.00407272	synonymous-codon	HERC1	GRCh38.p7	15:63775234	CTCCGGAGAATGCTG[C/T]TGCTGCTTCACCTTG	8925
rs761996121	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63643793	TTTCTACTCTTCAAA[C/G]TACAGAAATAACATC	8925
rs762008378	snp	C/T	1.65811e-05	0.00287929	intron-variant	HERC1	GRCh38.p7	15:63638686	GACTGAGAACCATCA[C/T]ACAGTTATCTTCATC	8925
rs762017394	snp	A/G	1.71814e-05	0.00293094	synonymous-codon	HERC1	GRCh38.p7	15:63692541	CCCTAGATGGAGTTC[A/G]GCTGCATGTTGTTTC	8925
rs762021125	in-del	-/C			intron-variant	HERC1	GRCh38.p7	15:63815714	TTACTCTGTTCAAAT[-/C]CCTCTAACCTAACAT	8925
rs762031561	snp	A/T	3.17234e-05	0.00398255	intron-variant	HERC1	GRCh38.p7	15:63696347	AAACGAAGCTTGAGG[A/T]AAAAAACATATTTTA	8925
rs762034553	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63823337	TAGATAGTATTTAAA[A/G]TCATGGAACTAAATA	8925
rs762036916	in-del	-/AAA	9.243e-05	0.00679753	intron-variant	HERC1	GRCh38.p7	15:63632850	CACAACTTTAAGAAG[-/AAA]AAAAATCACTCTTGA	8925
rs762055261	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63615738	GAAACCCAAGCATTC[A/T]TGTGTACCTCCCGAG	8925
rs762075148	snp	C/T	0.000213675	0.010334	intron-variant	HERC1	GRCh38.p7	15:63632602	CATAGTGACTACTCA[C/T]CACCTAGAACAAAAA	8925
rs762094219	snp	C/T	1.65685e-05	0.00287819	synonymous-codon	HERC1	GRCh38.p7	15:63674889	TAAAGCGGATTCACT[C/T]TCAGGTTTCTGCTCA	8925
rs762097769	snp	C/G	4.99476e-05	0.00499713	missense	HERC1	GRCh38.p7	15:63641565	CCAGAACACCCTGCT[C/G]TTTCAATGCTGTCCT	8925
rs762098109	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63811279	AGATACATGCCAATG[C/T]ACTGGGAGAGGACAG	8925
rs762117922	snp	A/G	1.80188e-05	0.00300151	synonymous-codon	HERC1	GRCh38.p7	15:63656127	TTTGGCAGCACTAGG[A/G]GCATTTGATGCCAGA	8925
rs762124793	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63677606	TTACCATTTTTTCCC[C/T]AAAACAAAACAGAAC	8925
rs762144711	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63609627	ATCCACCAAGAGGGT[A/G]CAGACTGGAAGCCAG	8925
rs762145494	snp	A/G	0.00033134	0.012867	synonymous-codon	HERC1	GRCh38.p7	15:63675018	GTCCAGCAGCACAGA[A/G]GCCGTCAGGCCTCGG	8925
rs762153196	snp	A/C/G	6.65528e-05	0.00576824	intron-variant	HERC1	GRCh38.p7	15:63694708	AAAATATAGAACATA[A/C/G]CTAGTACCATAACCT	8925
rs762158557	snp	A/G	1.95314e-05	0.00312495	missense	HERC1	GRCh38.p7	15:63756703	CGCAAGCTCTAACAG[A/G]GCCATCCGTAGAAAT	8925
rs762162129	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63722940	TAAAATGATTACCTA[C/T]AAATGTATTATATAA	8925
rs762170804	snp	A/G	0.00012785	0.00799429	missense	HERC1	GRCh38.p7	15:63649883	TCTGGCCAAGCCAGG[A/G]CAGATACCCAATGAG	8925
rs762177239	snp	A/C	1.6855e-05	0.00290297	intron-variant	HERC1	GRCh38.p7	15:63758156	ATCTACCAGTTTGTA[A/C]GCTATTTAGAAAACT	8925
rs762203755	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63780888	ATGAAAGTAGTTATG[A/G]CCCAAAATTTATAAT	8925
rs762207301	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63610462	GATTAACTCCTAGAA[C/T]GGCAGGAGTAGCCCA	8925
rs762208088	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63701767	TTGACATCAAAAAGA[C/T]TTAAAACACAAAAAT	8925
rs762208763	snp	A/G	1.66763e-05	0.00288753	missense	HERC1	GRCh38.p7	15:63674459	TCTTTATGGGTGACC[A/G]CATGACTGCTCGCTT	8925
rs762210376	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63797364	CAATATTTGTCACTT[C/T]CTCAATTACTCTTAT	8925
rs762211305	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63736386	AACTCTTTTTCCTCA[A/C]CAGAAGACTGTCACT	8925
rs762213636	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63658177	CCACAGTATCAACAC[A/G]GCAAGGATCCCCATG	8925
rs762222956	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63809899	TGCCCAGACTAGTCT[C/T]GAACCCCTGGGTTTA	8925
rs762232538	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63626869	TCTATGTGCCTGGCA[C/T]TATTCTAAGAGCTTT	8925
rs762265221	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63715273	GATGCTCTAAAAGCA[A/T]AGCTAGTTTAAAAAG	8925
rs762269396	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63832802	TTTGGAACAAATATA[C/G]AATGAGGAAGTCCCA	8925
rs762278446	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63794284	GACTCGCCCTGAATT[C/G]TTTCTTGCGTGAGAT	8925
rs762281460	snp	C/T	6.98739e-05	0.00591033	missense	HERC1	GRCh38.p7	15:63694012	AGTCAACTTTTTTTT[C/T]TTCTTCTTCACCGTC	8925
rs762298892	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63628018	TAAGGTGAGGAATTT[C/G]ACAAATGGTCTCAGG	8925
rs762302580	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63688095	AGAATGGACTTTAGG[A/G]CATAACAATGGAAGC	8925
rs762309385	snp	C/G	3.32884e-05	0.00407959	missense	HERC1	GRCh38.p7	15:63713371	GTCATAAGTCCACCC[C/G]CTTCAGAGGCACTTG	8925
rs762317701	in-del	-/A	9.34885e-05	0.00683634	intron-variant	HERC1	GRCh38.p7	15:63706843	CACTCTATTAAAAGT[-/A]AAAAGTAAATAAATA	8925
rs762325572	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63771390	AAATTAAGTCAAACA[A/C]ATATTCTTCCCCAGA	8925
rs762328232	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63793549	TGAATAATTCACCCC[C/T]TGTTTAGTATATAAT	8925
rs762339596	snp	A/G	3.94953e-05	0.00444365	synonymous-codon	HERC1	GRCh38.p7	15:63723225	GATCCAAAGGCTTCG[A/G]GCAGGCTCTTTAGAA	8925
rs762348880	snp	C/T	5.52217e-05	0.00525431	intron-variant	HERC1	GRCh38.p7	15:63656056	GTCAGAAATAATCAA[C/T]GTAACGGGGAAAAGT	8925
rs762358518	snp	C/T	1.66208e-05	0.00288273	missense	HERC1	GRCh38.p7	15:63678203	TGTGAAGCCTTTCCA[C/T]CATTTTTTTGTTAAT	8925
rs762364768	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63716232	AACTTTGCCTTTCTC[C/T]TTCAAGTTAGTTCCC	8925
rs762367428	snp	C/T	1.65677e-05	0.00287812	missense	HERC1	GRCh38.p7	15:63756486	TATTTCTGTGTTGAA[C/T]TATTTCCATGCCCCA	8925
rs762368673	snp	G/T			upstream-variant-2KB	HERC1	GRCh38.p7	15:63834640	TACATCCTTGATCAT[G/T]ACCTCGACCTCCACG	8925
rs762372617	snp	A/G	4.96866e-05	0.00498406	synonymous-codon	HERC1	GRCh38.p7	15:63661806	TAAGTACTTCTCCCT[A/G]CAGGTGCCACATAAC	8925
rs762381150	snp	A/G	1.65993e-05	0.00288086	missense	HERC1	GRCh38.p7	15:63663193	GGGCCTGCACAGAGC[A/G]GTATAATCCCGCTCA	8925
rs762389613	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63669935	CAGCAACAAAGCAGG[A/T]TGGGGGAATACAGCC	8925
rs762408566	snp	G/T	1.65751e-05	0.00287876	missense	HERC1	GRCh38.p7	15:63623793	CTTCTCCAACCAGCT[G/T]AACCTTCCACGCTCG	8925
rs762413762	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63804436	CTAAAAATACAAAAA[A/G]TTAGCCGGGCATGGT	8925
rs762419438	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63748433	AGCAGAGGGCTGAGT[C/T]ACATGATCTACTAAA	8925
rs762429253	snp	C/G	6.23267e-05	0.00558206	intron-variant	HERC1	GRCh38.p7	15:63723370	TCTAAAAAAAATACT[C/G]ACGTTACCAATTTTA	8925
rs762435271	snp	C/T	1.67407e-05	0.00289311	missense	HERC1	GRCh38.p7	15:63694543	AGAAGCAGACGTTGC[C/T]GGGCTTCTAAAAGAC	8925
rs762436545	snp	A/G	1.65674e-05	0.00287809	missense	HERC1	GRCh38.p7	15:63630569	ATGATTACTCCAGCC[A/G]GGACAGGGATTTGTT	8925
rs762504330	in-del	-/T			intron-variant	HERC1	GRCh38.p7	15:63816912	CATCACAAAGAGACA[-/T]TAAGACCTTACATAT	8925
rs762511572	snp	A/T	0.000321066	0.0126661	intron-variant	HERC1	GRCh38.p7	15:63622905	TCCTGCAGAAGAAAG[A/T]AAAAAATTTTTTGAG	8925
rs762522214	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63727149	GACGTGGTGGTGCAT[A/G]CCTGTAATCCCAGCT	8925
rs762524386	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63742576	AGGTTTTCAGTCTTT[C/T]TCCATTGAATATGAT	8925
rs762524456	snp	C/G	1.66007e-05	0.00288098	missense	HERC1	GRCh38.p7	15:63630485	CCTTCTGAATTGCTC[C/G]CCCAGGCATACACAT	8925
rs762539051	snp	C/G	1.66136e-05	0.00288211	missense	HERC1	GRCh38.p7	15:63678175	CCTGACTCTTTAATA[C/G]ATATCTTAATTTTGT	8925
rs762545706	in-del	-/AC	0.000151509	0.0087024	intron-variant	HERC1	GRCh38.p7	15:63732881	ACTAAAGAGATCCCT[-/AC]ACCCCTTTATTCTTT	8925
rs762549888	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63678649	TATAGAGACCAAGCC[A/G]TATATGACTGACTCA	8925
rs762551110	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63749954	GTTACAGCGATTTAT[A/C]ATGCTGCCTTTAGGC	8925
rs762551943	snp	C/T	1.77379e-05	0.00297802	synonymous-codon	HERC1	GRCh38.p7	15:63734802	CATCCGTTCTCGTAA[C/T]GGAGGTAACAGCATG	8925
rs762551956	snp	A/C/G			intron-variant	HERC1	GRCh38.p7	15:63761852	GTTTAAAAGGAAGAA[A/C/G]ATATAAATGTAAAGG	8925
rs762552821	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63681968	TCATGAGTGTATCAA[C/T]GTGTGGAGTCTGACG	8925
rs762566423	snp	C/G	3.56417e-05	0.00422133	synonymous-codon	HERC1	GRCh38.p7	15:63746960	GTCCATCAGTCTGAA[C/G]AGCAAATTTCGAAGT	8925
rs762578317	snp	C/T	2.04748e-05	0.00319953	intron-variant	HERC1	GRCh38.p7	15:63640482	TAATATGTCAAAGAG[C/T]TTGTGCCAAATATTC	8925
rs762587692	snp	C/T	1.65943e-05	0.00288043	missense	HERC1	GRCh38.p7	15:63663021	TCTGGGATCCACATT[C/T]CCAGAATATCATTGT	8925
rs762598633	in-del	-/A	0.0459686	0.144469	intron-variant	HERC1	GRCh38.p7	15:63712911	CTGTCTCACATGTAC[-/A]AAAAAAAAAGTTTTT	8925
rs762601724	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63698037	ATTTTAGCATTCAAC[A/T]GTGGGTCTTGATTGC	8925
rs762607231	snp	A/G	6.72348e-05	0.00579766	synonymous-codon	HERC1	GRCh38.p7	15:63712781	TATACCTACCAGTGC[A/G]TAACCCTCTTCATCT	8925
rs762622478	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63754889	ATGCTCCCCTCACAG[C/T]ACTTACCTTGTGTTG	8925
rs762623556	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63614007	GTCTGGAAAAAAAAT[C/T]AGGCTGAGGTATGGG	8925
rs762630889	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63631954	TTTTAGATGATACGA[A/G]TAAGGATTTAACTAC	8925
rs762640357	snp	C/G	1.65756e-05	0.00287881	missense	HERC1	GRCh38.p7	15:63678047	GCAGCTCTGAGAGGT[C/G]AGCGAGGCCATGCCT	8925
rs762646408	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63813807	GTATGGTGGCTCGCG[C/T]CTGTAATCCCAGCAC	8925
rs762650795	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63663735	AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACTG	8925
rs762675257	in-del	-/AAA			intron-variant	HERC1	GRCh38.p7	15:63809790	CTTGTTTAGAATAGC[-/AAA]AAAAAAAAAAAAAGT	8925
rs762677734	in-del	-/G	2.1017e-05	0.00324161	utr-variant-3-prime, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609060	GAGGGAGAGAAGGGA[-/G]GGGTGAGAGCACCCG	8925
rs762678022	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63675305	AAATGGGGAGATGTG[A/T]TACTAAATGCAGAAG	8925
rs762685480	snp	A/G	8.2814e-05	0.00643429	synonymous-codon	HERC1	GRCh38.p7	15:63672594	GGTGTCCTCCAGAGA[A/G]CTGCTCATAAAGGAG	8925
rs762686925	snp	C/T	1.66095e-05	0.00288175	missense	HERC1	GRCh38.p7	15:63658682	TCTCCTAACGTTATT[C/T]TCCCAGAGGAGCTCT	8925
rs762699628	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63785227	CCAGGAGTTCAAGAC[A/C]AGCCTGAGCAACATA	8925
rs762703598	in-del	-/AGA			downstream-variant-500B, cds-indel	HERC1, FBXL22	GRCh38.p7	15:63608381	GAGACCCAGGATGAC[-/AGA]AGAACAATGGAAAAT	8925
rs762716035	snp	A/G	6.83504e-05	0.00584555	intron-variant	HERC1	GRCh38.p7	15:63755337	CTACCTGCATTGCAC[A/G]CAAGTAAATACGATG	8925
rs762724831	snp	C/T	1.65861e-05	0.00287972	missense	HERC1	GRCh38.p7	15:63716430	GTTCGAGTAAATGAA[C/T]GCTCCTGAGGATCAA	8925
rs762730583	snp	A/T	3.77836e-05	0.00434631	missense	HERC1	GRCh38.p7	15:63655834	TGTGTTACAACAAAG[A/T]TTGGGGAGGTCACAA	8925
rs762742287	snp	A/G	1.65754e-05	0.00287879	missense	HERC1	GRCh38.p7	15:63752983	GATGTCAAAGCAAGT[A/G]AAGACTGGCTCCCAG	8925
rs762753239	snp	C/T	8.53588e-05	0.00653239	missense	HERC1	GRCh38.p7	15:63612265	CCCTATCAACCTTCA[C/T]GATTTGAAATCTCTG	8925
rs762758143	in-del	-/G			intron-variant	HERC1	GRCh38.p7	15:63760456	AAAAAAAAAAAAAAA[-/G]ACACAAAGGAAAAAC	8925
rs762759078	snp	A/G	0.000110807	0.00744253	missense	HERC1	GRCh38.p7	15:63652475	TAACATTCCATACGC[A/G]GATGGTGCCATCATT	8925
rs762775786	snp	C/T	1.65674e-05	0.00287809	synonymous-codon	HERC1	GRCh38.p7	15:63686410	TGCCAATCCATATCC[C/T]TTCCCTCCACTGCCG	8925
rs762777172	in-del	-/A	1.6996e-05	0.00291508	intron-variant	HERC1	GRCh38.p7	15:63630638	CTATCAGGCGATCTG[-/A]AAAAAAACAAAACAA	8925
rs762783747	snp	A/G	0.000877694	0.0209303	synonymous-codon	HERC1	GRCh38.p7	15:63635984	CTTCTTCTCCTTGTA[A/G]GGCCTCGATCTGCCT	8925
rs762796759	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63826325	TTTAATTTTCATTAC[A/G]ACTGCCCTTCTTCCT	8925
rs762804702	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63631000	CTTTTTTGAGACAGG[A/G]TCTCGCTCTGTCGCC	8925
rs762807082	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63825098	GAGATCACTTGAGGC[C/T]GGGAGTTCGAGAGCA	8925
rs762807710	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63741591	GGATTACAGGCGTGC[A/G]CCTGGCCCTATGTTT	8925
rs762820244	snp	A/C	1.66112e-05	0.00288189	missense	HERC1	GRCh38.p7	15:63727747	GTCGAGGAGGTAACT[A/C]AATAAAGGCCGAGCC	8925
rs762822835	snp	A/T	1.65616e-05	0.00287759	missense	HERC1	GRCh38.p7	15:63645011	CAATTTGATTCCTGC[A/T]CCCACCATCCTTCTG	8925
rs762837087	snp	C/G	3.41548e-05	0.00413234	synonymous-codon	HERC1	GRCh38.p7	15:63626138	AGGCAGGCCCAGCTG[C/G]AGAGGTACTGACACA	8925
rs762845417	snp	C/T	0.000134312	0.00819379	intron-variant	HERC1	GRCh38.p7	15:63698681	CATTCAATGGTTCAG[C/T]TTTAAGTTTCCAGAG	8925
rs762846628	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63806905	GGCATGCGCCACCGC[A/G]CCCGGCTAAGTTTTA	8925
rs762861130	snp	C/T	3.31444e-05	0.00407076	missense	HERC1	GRCh38.p7	15:63664490	CTTGCTAGCAGTGTG[C/T]GAGCAGCTAAGTCAA	8925
rs762866694	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63721245	CAAACAAAATGGGGC[C/G]AGGCGCCGTGGCTCA	8925
rs762868809	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63707510	ACTTGGCCTATATGT[A/G]CAGGCAACCATAAAC	8925
rs762899154	snp	G/T	3.67134e-05	0.00428432	intron-variant	HERC1	GRCh38.p7	15:63656064	TAATCAATGTAACGG[G/T]GAAAAGTACTGAAAG	8925
rs762915282	snp	A/G	3.74525e-05	0.00432722	synonymous-codon	HERC1	GRCh38.p7	15:63723248	CTTTAGAACAACCCA[A/G]TGCCAAGTCTACATA	8925
rs762918341	snp	G/T	1.66214e-05	0.00288278	missense	HERC1	GRCh38.p7	15:63658582	TCTCATGACCATGGT[G/T]CTGGCCAGAAGAACC	8925
rs762919308	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63732074	TGGTGCGACCTCAGC[C/T]CACTTCAGCCTCTGC	8925
rs762926694	snp	C/T	2.32588e-05	0.00341011	synonymous-codon	HERC1	GRCh38.p7	15:63764150	CAAGCCATCCGATGT[C/T]CTGGTTGGTTCTCTC	8925
rs762932940	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63699574	TATAAGGAACATTCT[C/T]ACTGACTGTGTCATG	8925
rs762974420	snp	C/G			intron-variant	HERC1	GRCh38.p7	15:63802453	AACTACAGACAAAAT[C/G]AAATCAAACTAATGG	8925
rs762982164	snp	A/T	3.31581e-05	0.00407161	missense	HERC1	GRCh38.p7	15:63686501	ACTTCTTGGATAGGA[A/T]GATTCTCATCTTCTT	8925
rs762989422	snp	C/G			missense	HERC1	GRCh38.p7	15:63654202	TCTGCAGAGTAGTTT[C/G]GTTGTCACGGTCGTG	8925
rs763011437	snp	A/T	1.65649e-05	0.00287788	missense	HERC1	GRCh38.p7	15:63674908	GGTTTCTGCTCAACA[A/T]CCCCTTTCTCCTCGG	8925
rs763014582	snp	C/G	3.31625e-05	0.00407188	synonymous-codon	HERC1	GRCh38.p7	15:63616484	GTGAAGAATGCTGTT[C/G]AGAGTCTGCACGTAG	8925
rs763016052	in-del	-/A	1.6916e-05	0.00290822	intron-variant	HERC1	GRCh38.p7	15:63651207	TAAGAAGAAGGCTTT[-/A]AAAAAACTACTTTCA	8925
rs763026684	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63818265	TAGTCCTATGGGCCT[A/G]TGGTACTTCTGGAAT	8925
rs763028090	snp	C/T	1.92332e-05	0.003101	intron-variant	HERC1	GRCh38.p7	15:63628650	AAAAAAGAAACGCTG[C/T]AGGAGCATGAATATT	8925
rs763038691	snp	A/C/T	3.33585e-05	0.00408391	missense	HERC1	GRCh38.p7	15:63732959	TTAAGAGGGTCTTCA[A/C/T]CAAAATTTCAGCCAG	8925
rs763041554	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63819415	AAACTATAAATAAAT[A/G]TAAGTTGTTATTCTC	8925
rs763060154	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63711493	GAGAAAAGGAGGAAG[G/T]ATAAACAAAATGTCA	8925
rs763061884	snp	C/G	1.65638e-05	0.00287778	missense	HERC1	GRCh38.p7	15:63733027	TGATCTGACAGATTT[C/G]CGTAGCCAGTACACA	8925
rs763066065	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63746815	AGTAAGGGAAACAAC[A/C]TCCAATTGAAATTGT	8925
rs763076398	snp	A/C	1.66704e-05	0.00288703	synonymous-codon	HERC1	GRCh38.p7	15:63775378	TAGCTGGCTGCTAAG[A/C]AGGGCATCCAAATAG	8925
rs763077309	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63829874	AACAATTTGAACAAC[A/G]AAATAAATAATGATA	8925
rs763077626	snp	G/T	5.62224e-05	0.0053017	missense	HERC1	GRCh38.p7	15:63694143	ACTTTGGGACTCAGT[G/T]TATCAGCATAGGTCC	8925
rs763098306	snp	A/G	2.96582e-05	0.00385074	intron-variant	HERC1	GRCh38.p7	15:63756753	CCAGCTTCAATCTAT[A/G]AACAAAGAATCATAA	8925
rs763100547	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63831068	GTATTTCATGTGTAT[A/G]TTAAGCCAAAGTTGT	8925
rs763103139	snp	C/T	1.6729e-05	0.00289209	intron-variant	HERC1	GRCh38.p7	15:63616426	TAGACTGGCCAGGAT[C/T]TACCTCATGGAAACT	8925
rs763107821	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63801560	ACTATCAGAGCAGAG[A/G]CAGTATCGATTTTGC	8925
rs763111827	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63791425	ATGCCTTGTACAAAC[A/G]GAAAGATGAATCATC	8925
rs763112515	in-del	-/C	1.67075e-05	0.00289023	intron-variant	HERC1	GRCh38.p7	15:63663217	CCGCTCAGAACAAAA[-/C]AAAAAAGGCATTTTA	8925
rs763112776	in-del	-/ATT			intron-variant	HERC1	GRCh38.p7	15:63639513	GAACATATCCCCATC[-/ATT]AAGTGATGCATAGCT	8925
rs763115570	snp	G/T			intron-variant	HERC1	GRCh38.p7	15:63778238	CAGACTAAGAAAAAC[G/T]GCAGAAAAGACAGAG	8925
rs763129984	snp	C/G/T	3.31434e-05	0.00407073	missense	HERC1	GRCh38.p7	15:63775518	GTTTAGAATACAGAA[C/G/T]AGCAACTCCCTCTCT	8925
rs763130759	snp	A/G	3.3123e-05	0.00406945	synonymous-codon	HERC1	GRCh38.p7	15:63661823	AGGTGCCACATAACA[A/G]GTAGTACGGATTTCC	8925
rs763153485	snp	C/T	3.39795e-05	0.00412172	intron-variant	HERC1	GRCh38.p7	15:63723378	AAATACTCACGTTAC[C/T]AATTTTAACATCATA	8925
rs763154971	snp	C/T	2.60014e-05	0.00360555	intron-variant	HERC1	GRCh38.p7	15:63645435	ATGCAGATAACAGTC[C/T]ATACCAATATAAAAA	8925
rs763158378	snp	C/T	1.97155e-05	0.00313964	intron-variant	HERC1	GRCh38.p7	15:63632673	CAATGTTTATAATGA[C/T]GTGTACCCAAGCAAA	8925
rs763178353	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63759093	GGCCATTTTTAAGGA[C/T]ATAGTTGTTACTATA	8925
rs763187373	in-del	-/TC			intron-variant	HERC1	GRCh38.p7	15:63735990	ACTAAATGCACATAT[-/TC]TGTTTCCAAAAGCCC	8925
rs763194040	snp	A/C	1.71708e-05	0.00293003	intron-variant	HERC1	GRCh38.p7	15:63749355	AGAATTTTTAAACAT[A/C]GGCACTCTTACCTGT	8925
rs763205489	in-del	-/G			intron-variant	HERC1	GRCh38.p7	15:63733857	ACCCTGTCTCAAAAA[-/G]AAAAATAAAAAAATC	8925
rs763224069	snp	C/T	3.31455e-05	0.00407083	missense	HERC1	GRCh38.p7	15:63624246	GCACCATTGGCAGAG[C/T]GTAGACTCTTGGGGC	8925
rs763250509	snp	C/T	1.68525e-05	0.00290275	intron-variant	HERC1	GRCh38.p7	15:63636190	TGGATGTTAAAACTC[C/T]CCTCTTTACTTGCAG	8925
rs763259633	snp	A/G	1.66849e-05	0.00288828	intron-variant	HERC1	GRCh38.p7	15:63666487	GCTGAGACAAAAGGA[A/G]GAGAAATAAGAACCT	8925
rs763266005	snp	G/T	3.35661e-05	0.00409657	missense	HERC1	GRCh38.p7	15:63675077	CACAGGGTTCCAGAT[G/T]ATACAATGGAGTATC	8925
rs763279541	snp	C/G	1.67332e-05	0.00289246	missense	HERC1	GRCh38.p7	15:63651278	CCAGATATTCACCAT[C/G]TTTTCCAAAGCGCCT	8925
rs763291356	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63749169	ATGACTTCTTGCTTC[A/G]GAAACATGTCTAACC	8925
rs763303775	in-del	-/AATGGACAAGCTTT			intron-variant	HERC1	GRCh38.p7	15:63638319	CATAATAGATTATGA[-/AATGGACAAGCTTT]ATCCCACAATAAGAC	8925
rs763313292	snp	C/T	1.66037e-05	0.00288125	intron-variant	HERC1	GRCh38.p7	15:63669533	GTGCATATCAGCACA[C/T]GCACCTGTGCGGTTA	8925
rs763319093	snp	A/C/T	4.97387e-05	0.00498671	missense	HERC1	GRCh38.p7	15:63758201	CAGAGAAACTAGGAG[A/C/T]CAGTTTGGGTTGCAG	8925
rs763332375	snp	C/T	0.000137675	0.00829568	intron-variant	HERC1	GRCh38.p7	15:63643091	TACCAATACACACCA[C/T]TGAACTGTAGGTATA	8925
rs763352227	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63679361	ATTTTTAAAAACATA[A/G]AATAAAAGGTAATTT	8925
rs763352649	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63648761	GAACTGAGTAGACAG[A/G]AGAAAGACTTTTCAC	8925
rs763361099	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63769737	GGCGGGCACCTGTAA[A/T]CCCAGCTACTTGGGA	8925
rs763363065	snp	C/T	0.000143599	0.00847224	intron-variant	HERC1	GRCh38.p7	15:63729196	AAGTGTTCTTACTTC[C/T]TAATGACTGATTAAA	8925
rs763373285	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63824839	GTGACACAAGTCAGA[C/T]GTAGGAAAAAAAAAA	8925
rs763390207	snp	A/G	1.65759e-05	0.00287883	synonymous-codon	HERC1	GRCh38.p7	15:63749471	CTTTGGTTTAGTAAT[A/G]GGACCTGTGGAATTT	8925
rs763390920	snp	A/C			intron-variant	HERC1	GRCh38.p7	15:63724854	AAAAATTAGGACATA[A/C]TATAATGTCAGCATG	8925
rs763402638	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63782166	AAGTAGTTATATTAA[A/T]CAACAGATTTTCAAT	8925
rs763413099	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63703705	GACTGAGCAACATGG[C/T]GAAACCCCGTTTCTA	8925
rs763415833	snp	A/G	0.000270613	0.011629	intron-variant	HERC1	GRCh38.p7	15:63680193	TGAGGAAAAGAAAAA[A/G]GAAATAGAAATTTTT	8925

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